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Sample records for carbonate crystals precipitated

  1. Graphene crystal growth by thermal precipitation of focused ion beam induced deposition of carbon precursor via patterned-iron thin layers

    Directory of Open Access Journals (Sweden)

    Rius Gemma

    2014-01-01

    Full Text Available Recently, relevant advances on graphene as a building block of integrated circuits (ICs have been demonstrated. Graphene growth and device fabrication related processing has been steadily and intensively powered due to commercial interest; however, there are many challenges associated with the incorporation of graphene into commercial applications which includes challenges associated with the synthesis of this material. Specifically, the controlled deposition of single layer large single crystal graphene on arbitrary supports, is particularly challenging. Previously, we have reported the first demonstration of the transformation of focused ion beam induced deposition of carbon (FIBID-C into patterned graphitic layers by metal-assisted thermal treatment (Ni foils. In this present work, we continue exploiting the FIBID-C approach as a route for graphene deposition. Here, thin patterned Fe layers are used for the catalysis of graphenization and graphitization. We demonstrate the formation of high quality single and few layer graphene, which evidences, the possibility of using Fe as a catalyst for graphene deposition. The mechanism is understood as the minute precipitation of atomic carbon after supersaturation of some iron carbides formed under a high temperature treatment. As a consequence of the complete wetting of FIBID-C and patterned Fe layers, which enable graphene growth, the as-deposited patterns do not preserve their original shape after the thermal treatment

  2. Study of calcium carbonate and sulfate co-precipitation

    KAUST Repository

    Zarga, Y.

    2013-06-01

    Co-precipitation of mineral based salts in scaling is still not well understood and/or thermodynamically well defined in the water industry. This study focuses on investigating calcium carbonate (CaCO3) and sulfate mixed precipitation in scaling which is commonly observed in industrial water treatment processes including seawater desalination either by thermal-based or membrane-based processes. Co-precipitation kinetics were studied carefully by monitoring several parameters simultaneously measured, including: pH, calcium and alkalinity concentrations as well as quartz microbalance responses. The CaCO3 germination in mixed precipitation was found to be different than that of simple precipitation. Indeed, the co-precipitation of CaCO3 germination time was not anymore related to supersaturation as in a simple homogenous precipitation, but was significantly reduced when the gypsum crystals appeared first. On the other hand, the calcium sulfate crystals appear to reduce the energetic barrier of CaCO3 nucleation and lead to its precipitation by activating heterogeneous germination. However, the presence of CaCO3 crystals does not seem to have any significant effect on gypsum precipitation. IR spectroscopy and the Scanning Electronic Microscopy (SEM) were used to identify the nature of scales structures. Gypsum was found to be the dominant precipitate while calcite and especially vaterite were found at lower proportions. These analyses showed also that gypsum crystals promote calcite crystallization to the detriment of other forms. © 2013 Elsevier Ltd.

  3. Ice crystal precipitation at Dome C site (East Antarctica)

    Science.gov (United States)

    Santachiara, G.; Belosi, F.; Prodi, F.

    2016-01-01

    For the first time, falling ice crystals were collected on glass slides covered with a thin layer of 2% formvar in chloroform at the Dome Concordia site (Dome C), Antarctica. Samplings were performed in the framework of the 27th Italian Antarctica expedition of the Italian National Program for Research in Antarctica in the period 21 February-6 August 2012. Events of clear-sky precipitations and precipitations from clouds were considered and the replicas obtained were examined under Scanning Electron Microscope (SEM). Several shapes of ice crystals were identified, including "diamond dust" (plates, pyramids, hollow and solid columns), and crystal aggregates varying in complexity. Single events often contained both small (10 μm to 50 μm) and large (hundreds of microns) crystals, suggesting that crystals can form simultaneously near the ground (height of a few hundred metres) and at higher layers (height of thousands of metres). Images of sampled crystal replicas showed that single bullets are not produced separately, but by the disintegration of combinations of bullets. Rimed ice crystals were absent in the Dome C samples, i.e. the only mode of crystal growth was water vapour diffusion. On considering the aerosol in the sampled crystals, we reached the conclusion that inertial impaction, interception and Brownian motion were insufficient to explain the scavenged aerosol. We therefore presume that phoretic forces play a role in scavenging during the crystal growth process.

  4. INDUSTRIAL CRYSTALLIZATION AND PRECIPITATION FROM SOLUTIONS: STATE OF THE TECHNIQUE

    Directory of Open Access Journals (Sweden)

    M. Giulietti

    2001-12-01

    Full Text Available Crystallization and precipitation from solutions are responsible for 70% of all solid materials produced by the chemical industry. Competing with distillation as a separation and purification technique, their use is widespread. They operate at low temperatures with low energy consumption and yield with high purifications in one single step. Operational conditions largely determine product quality in terms of purity, filterability, flowability and reactivity. Producing a material with the desired quality often requires a sound knowledge of the elementary steps involved in the process: creation of supersaturation, nucleation, crystal growth, aggregation and other secondary processes. Mathematical models coupling these elementary processes to all particles in a crystallizer have been developed to design and optimize crystallizer operation. For precipitation, the spatial distribution of reactants and particles in the reactor is important; thus the tools of computational fluid dynamics are becoming increasingly important. For crystallization of organic chemicals, where incorporation of impurities and crystal shape are critical, molecular modeling has recently appeared as a useful tool. These theoretical developments must be coupled to experimental data specific to each material. Theories and experimental techniques of industrial crystallization and precipitation from solutions are reviewed, and recent developments are highlighted.

  5. Effects of DPPC/Cholesterol liposomes on the properties of freshly precipitated calcium carbonate.

    Science.gov (United States)

    Szcześ, A

    2013-01-01

    DPPC/Cholesterol liposomes of average diameter below 100nm were used as a matrix for calcium carbonate precipitation. Adsorption of calcium ions on the vesicles was determined via zeta potential measurement. It was found that with increasing calcium ions concentration the electrokinetic potential of the vesicles varied toward more positive values. The changes became smaller with the cholesterol content increase. Accumulation of calcium ions close to the vesicles membranes lead to attraction of CO(3)(2-) ions and enhances nucleation and growth of small calcium carbonate crystals that aggregates within lipid vesicles forming porous balls aggregates. However, dipalmitoylphosphatidylcholine (DPPC) does not change the CaCO(3) crystal forms and calcite is the only form obtained during precipitation. Moreover, the influence of the phospholipid on the calcium carbonate precipitation is enhanced by the induction of cholesterol to the lipid membranes. PMID:22796770

  6. Microbially Mediated-Precipitation of Cadmium Carbonate Nanoparticles.

    Science.gov (United States)

    Kang, Serku; Kim, Yumi; Lee, Youngjae; Rohl, Yul

    2015-01-01

    The objectives of this study were to investigate the microbially mediated precipitation of cadmium using microorganisms enriched from rhodoliths and to characterize the mineralogical properties of the precipitates. A 16S rRNA sequence analysis showed the enriched microorganisms contained carbonate forming microorganisms such as Proteus mirabilis. The microorganisms mediated Cd-precipitation with Cd-acetate, but no precipitates were formed without the microbes in D-1 medium. XRD analysis showed the precipitates were poorly crystalline Cd-carbonates (CdCO3). SEM and TEM-EDS analyses showed that the Cd-carbonate minerals were irregular in shape, 20-30 nm in size, and composed of C, O, and Cd. Therefore, microbially mediated precipitation of cadmium carbonates could be used as a precursor of CdO nanoparticles and could play an important role in Cd immobilization in Cd-contaminated water as well as CO2 fixation in natural environments.

  7. Control of calcium carbonate precipitation in anaerobic reactors.

    OpenAIRE

    Langerak, van, B.

    1998-01-01

    Anaerobic treatment of waste waters with a high calcium content may lead to excessive precipitation of calcium carbonate. So far, no proper methods were available to predict or reduce the extent of precipitation in an anaerobic treatment system. Moreover, it also was not clear to what extent precipitation in an anaerobic reactor can be tolerated because adequate knowledge on the structure and quality of methanogenic sludges with high calcium carbonate content was lacking. In this thesis, the ...

  8. Control of calcium carbonate precipitation in anaerobic reactors.

    NARCIS (Netherlands)

    Langerak, van E.P.A.

    1998-01-01

    Anaerobic treatment of waste waters with a high calcium content may lead to excessive precipitation of calcium carbonate. So far, no proper methods were available to predict or reduce the extent of precipitation in an anaerobic treatment system. Moreover, it also was not clear to what extent precipi

  9. Biogrout, ground improvement by microbial induced carbonate precipitation

    NARCIS (Netherlands)

    Van Paassen, L.A.

    2009-01-01

    Biogrout is a new ground improvement method based on microbially induced precipitation of calcium carbonate (MICP). When supplied with suitable substrates, micro-organisms can catalyze biochemical conversions in the subsurface resulting in precipitation of inorganic minerals, which change the mechan

  10. DISSOLUTION OF PLUTONIUM CONTAINING CARRIER PRECIPITATE BY CARBONATE METATHESIS AND SEPARATION OF SULFIDE IMPURITIES THEREFROM BY SULFIDE PRECIPITATION

    Science.gov (United States)

    Duffield, R.B.

    1959-07-14

    A process is described for recovering plutonium from foreign products wherein a carrier precipitate of lanthanum fluoride containing plutonium is obtained and includes the steps of dissolving the carrier precipitate in an alkali metal carbonate solution, adding a soluble sulfide, separating the sulfide precipitate, adding an alkali metal hydroxide, separating the resulting precipitate, washing, and dissolving in a strong acid.

  11. Synthesis of BiFeO3 by carbonate precipitation

    Indian Academy of Sciences (India)

    V Kothai; Rajeev Ranjan

    2012-04-01

    Magnetoelectric multiferroic BiFeO3 (BFO) was synthesized by a simple carbonate precipitation technique of metal nitrate solutions. X-ray powder diffraction and thermo-gravimetric analysis (TGA) revealed that the precipitate consists of an intimate mixture of crystalline bismuth carbonate and an amorphous hydroxide of iron. The precipitate yielded BiFeO3 at an optimal calcination temperature of ∼560°C. Energy dispersive X-ray (EDX) analysis showed 1:1 ratio between Bi and Fe in the oxide. X-ray photoelectron spectroscopy (XPS) studies confirmed that Fe to be in +3 oxidation states both in the precipitated powder and BiFeO3. The synthesized BFO exhibits a very weak ferromagnetic correlation at room temperature and the degree of which increases slightly on cooling down to 10 K suggesting alteration in the long range spatial modulation of the spins arrangement as compared to the bulk BiFeO3.

  12. The skeletal organic matrix from Mediterranean coral Balanophyllia europaea influences calcium carbonate precipitation.

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    Stefano Goffredo

    Full Text Available Scleractinian coral skeletons are made mainly of calcium carbonate in the form of aragonite. The mineral deposition occurs in a biological confined environment, but it is still a theme of discussion to what extent the calcification occurs under biological or environmental control. Hence, the shape, size and organization of skeletal crystals from the cellular level through the colony architecture, were attributed to factors as diverse as mineral supersaturation levels and organic mediation of crystal growth. The skeleton contains an intra-skeletal organic matrix (OM of which only the water soluble component was chemically and physically characterized. In this work that OM from the skeleton of the Balanophyllia europaea, a solitary scleractinian coral endemic to the Mediterranean Sea, is studied in vitro with the aim of understanding its role in the mineralization of calcium carbonate. Mineralization of calcium carbonate was conducted by overgrowth experiments on coral skeleton and in calcium chloride solutions containing different ratios of water soluble and/or insoluble OM and of magnesium ions. The precipitates were characterized by diffractometric, spectroscopic and microscopic techniques. The results showed that both soluble and insoluble OM components influence calcium carbonate precipitation and that the effect is enhanced by their co-presence. The role of magnesium ions is also affected by the presence of the OM components. Thus, in vitro, OM influences calcium carbonate crystal morphology, aggregation and polymorphism as a function of its composition and of the content of magnesium ions in the precipitation media. This research, although does not resolve the controversy between environmental or biological control on the deposition of calcium carbonate in corals, sheds a light on the role of OM, which appears mediated by the presence of magnesium ions.

  13. Precipitation of calcium carbonate in aqueous solutions in presence of ethylene glycol and dodecane.

    Science.gov (United States)

    Natsi, Panagiota D.; Rokidi, Stamatia; Koutsoukos, Petros G.

    2015-04-01

    The formation of calcium carbonate (CaCO3) in aqueous supersaturated solutions has been intensively studied over the past decades, because of its significance for a number of processes of industrial and environmental interest. In the oil and gas production industry the deposition of calcium carbonate affects adversely the productivity of the wells. Calcium carbonate scale deposits formation causes serious problems in water desalination, CO2 sequestration in subsoil wells, in geothermal systems and in heat exchangers because of the low thermal coefficient of the salt. Amelioration of the operational conditions is possible only when the mechanisms underlying nucleation and crystal growth of calcium carbonate in the aqueous fluids is clarified. Given the fact that in oil production processes water miscible and immiscible hydrocarbons are present the changes of the dielectric constant of the fluid phase has serious impact in the kinetics of calcium carbonate precipitation, which remains largely unknown. The problem becomes even more complicated if polymorphism exhibited by calcium carbonate is also taken into consideration. In the present work, the stability of aqueous solutions supersaturated with respect to all calcium carbonate polymorphs and the subsequent kinetics of calcium carbonate precipitation were measured. The measurements included aqueous solutions and solutions in the presence of water miscible (ethylene glycol, MEG) and water immiscible organics (n-dodecane). All measurements were done at conditions of sustained supersaturation using the glass/ Ag/AgCl combination electrode as a probe of the precipitation and pH as the master variable for the addition of titrant solutions with appropriate concentration needed to maintenance the solution supersaturation. Initially, the metastable zone width was determined from measurements of the effect of the solution supersaturation on the induction time preceding the onset of precipitation at free-drift conditions. The

  14. Surface precipitates formed on annealed LSAT (001) single crystal.

    Science.gov (United States)

    Ohashi, Kazuki; Okada, Shunsuke; Sasaki, Katsuhiro; Tokunaga, Tomoharu; Kobayashi, Shunsuke; Yamamoto, Takahisa

    2014-11-01

    LSAT (La0.3Sr0.7)(Al0.65Ta0.35)O3, which has a complex perovskite structure of (A'A'')(B'B'')O3, is expected as an attracting substrates for GaN and high temperature superconductivity oxides solid thin films from a viewpoint of the suitable lattice matching. To grow high quality thin film, it is very important to prepare step-terrace structure on substrates used for thin film growth. For this purpose, a technique of annealing substrates with mirror surface is often used. However, surface precipitates, called surface mounts, are reported to appear after annealing LSAT substrates [1]. In this study, we investigated the surface precipitates formed on annealed LSAT surfaces by TEM/STEM. Further, we directly confirmed the terminated atomic layers at the annealed LSAT surfaces in the area without surface precipitates.Commercially available LSAT single crystal substrates with (001) surfaces (SHINKOSHA CO.,LTD) were used for TEM/STEM observation. After annealing at 1300°C for 30 min in air, the (001) surface structures were observed from [110] direction using cross sectional thin foils. The thin foils were prepared by joining two annealed LSAT (001) surfaces with glue, grinding, polishing and finally Ar ion milling. TEM/STEM observation was conducted by JEOL ARM-200F (a double Cs-corrector type for TEM/STEM) operated at 200kV.Surface mounds were confirmed to appear on LSAT crystal surface after annealing at the annealing condition used in this study. A typical example is shown in Fig. 1. shows TEM bright field image taken from the surface area of LSAT (001) after annealing. The observation direction of the image is [110], which is parallel to the annealed surface. Cross sectional images of surface mounts with 300nm was clearly seen as indicated by the arrows in the image. The height of the mounts is around 20nm, and it is noted that the interfaces between the mounts and LSAT surfaces are hollowed into LSAT crystal with the depth about 10nm. Nano diffractometric and EDS

  15. Small angle neutron scattering (SANS) study of γ' precipitates in single crystals of AM1 superalloy

    OpenAIRE

    Bellet, D; Bastie, P.; Royer, A.; Lajzerowicz, J.; Legrand, J.; Bonnet, R.

    1992-01-01

    The morphology of γ' precipitates of AM1 single crystal superalloys has been studied by small neutron scattering (SANS), and electron microscopy. Due to the single crystal nature of the samples, the SANS patterns are anisotropic and exhibit a fourfold symmetry corresponding both to the shape and to the spatial arrangement of the precipitates in a (001) plane. Measurements for other sample orientations have allowed us to improve the analysis of the shape of the precipitates. After creep deform...

  16. Formate oxidation driven calcium carbonate precipitation by Methylocystis parvus OBBP

    NARCIS (Netherlands)

    Ganendra, G; De Muynck, W; Ho, A.; Arvaniti, EC; Hosseinkhani, B; Ramos, JA; Rahier, H; Boon, N.

    2014-01-01

    Microbially Induced Carbonate Precipitation (MICP) applied in the construction industry poses several disadvantages such as ammonia release to the air and nitric acid production. An alternative MICP from calcium formate by Methylocystis parvus OBBP is presented in this study to overcome these disadv

  17. Microbially-Mediated Precipitation of Calcium Carbonate Nanoparticles.

    Science.gov (United States)

    Kang, Ser Ku; Roh, Yul

    2016-02-01

    The objective of this study was to investigate the biomineralization of carbonate minerals using microorganisms (Wu Do-1) enriched from rhodoliths. A 16S rRNA sequence analysis showed that Wu Do-1 mainly contained Proteus mirabilis. The pH decreased from 6.5 to 5.3 over the first 4 days of incubation due to microbial oxidation of organic acids, after which it increased to 7.8 over the remaining incubation period. XRD analysis showed that the precipitates were Mg-rich cal- cite (MgxCa(1-x)CO3), whereas no precipitates were formed without the addition of Wu Do-1 in D-1 medium. SEM-EDS analyses showed that the Mg-rich calcite had a rhombohedron shape and consisted of Ca, Si and Mg with an extracelluar polymeric substance (EPS). In addition, TEM-EDS analyses revealed they were hexagon in shape, 500-700 nm in size, and composed of Ca, Mg, C, and O. These results indicated that Wu Do-1 induced precipitation of Mg-rich calcite on the cell walls and EPS via the accumulation of Ca and/or Mg ions. Therefore, microbial precipitation of carbonate nanoparticles may play an important role in metal and carbon biogeochemistry, as well as in carbon sequestration in natural environments.

  18. Model of apparent crystal growth rate and kinetics of seeded precipitation from sodium aluminate solution

    Institute of Scientific and Technical Information of China (English)

    LI Xiao-bin; LIU Zhi-jian; XU Xiao-hui; ZHOU Qiu-sheng; PENG Zhi-hong; LIU Gui-hua

    2005-01-01

    Based on the population balance equation in a batch crystallizer characteristic of seeded precipitation, a model to calculate the rate of apparent crystal growth of aluminum hydroxide from the size distribution was deve-loped. The simulation results indicate that the rate of apparent crystal growth during seeded precipitation exhibits a manifest dependence on the crystal size. In general, there is an obvious increase in the apparent crystal growth rate with the augment in crystal size. The apparent activation energy increases with the increase of characteristic crystal size, which indicates that the growth of small crystals is controlled by surface chemical reaction; it is gradually controlled by both the surface reaction and diffusion with the augment in crystal size.

  19. Microscopic modelling of simultaneous two-phase precipitation: application to carbide precipitation in low-carbon steels

    International Nuclear Information System (INIS)

    A thermodynamically-based precipitation model, employing the classical nucleation and growth theories, has been adapted to deal with simultaneous precipitation of metastable and stable phases. This model gives an estimation of the precipitation kinetics (time evolution of radius and density of precipitates for both phases, as well as the evolution of solute fraction) in a wide range of temperature. Results were successfully compared with an experimental isothermal precipitation diagram (Time-Temperature-Transformation, TTT) from the literature for the precipitation of ε carbide and Fe3C in low-carbon steels

  20. Magnesium isotope fractionation in bacterial mediated carbonate precipitation experiments

    Science.gov (United States)

    Parkinson, I. J.; Pearce, C. R.; Polacskek, T.; Cockell, C.; Hammond, S. J.

    2012-12-01

    Magnesium is an essential component of life, with pivotal roles in the generation of cellular energy as well as in plant chlorophyll [1]. The bio-geochemical cycling of Mg is associated with mass dependant fractionation (MDF) of the three stable Mg isotopes [1]. The largest MDF of Mg isotopes has been recorded in carbonates, with foraminiferal tests having δ26Mg compositions up to 5 ‰ lighter than modern seawater [2]. Magnesium isotopes may also be fractionated during bacterially mediated carbonate precipitation and such carbonates are known to have formed in both modern and ancient Earth surface environments [3, 4], with cyanobacteria having a dominant role in carbonate formation during the Archean. In this study, we aim to better constrain the extent to which Mg isotope fractionation occurs during cellular processes, and to identify when, and how, this signal is transferred to carbonates. To this end we have undertaken biologically-mediated carbonate precipitation experiments that were performed in artificial seawater, but with the molar Mg/Ca ratio set to 0.6 and with the solution spiked with 0.4% yeast extract. The bacterial strain used was marine isolate Halomonas sp. (gram-negative). Experiments were run in the dark at 21 degree C for two to three months and produced carbonate spheres of various sizes up to 300 μm in diameter, but with the majority have diameters of ~100 μm. Control experiments run in sterile controls (`empty` medium without bacteria) yielded no precipitates, indicating a bacterial control on the precipitation. The carbonate spheres are produced are amenable to SEM, EMP and Mg isotopic analysis by MC-ICP-MS. Our new data will shed light on tracing bacterial signals in carbonates from the geological record. [1] Young & Galy (2004). Rev. Min. Geochem. 55, p197-230. [2] Pogge von Strandmann (2008). Geochem. Geophys. Geosys. 9 DOI:10.1029/2008GC002209. [3] Castanier, et al. (1999). Sed. Geol. 126, 9-23. [4] Cacchio, et al. (2003

  1. Amorphous calcium carbonate precipitation by cellular biomineralization in mantle cell cultures of Pinctada fucata.

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    Liang Xiang

    Full Text Available The growth of molluscan shell crystals is generally thought to be initiated from the extrapallial fluid by matrix proteins, however, the cellular mechanisms of shell formation pathway remain unknown. Here, we first report amorphous calcium carbonate (ACC precipitation by cellular biomineralization in primary mantle cell cultures of Pinctada fucata. Through real-time PCR and western blot analyses, we demonstrate that mantle cells retain the ability to synthesize and secrete ACCBP, Pif80 and nacrein in vitro. In addition, the cells also maintained high levels of alkaline phosphatase and carbonic anhydrase activity, enzymes responsible for shell formation. On the basis of polarized light microscopy and scanning electron microscopy, we observed intracellular crystals production by mantle cells in vitro. Fourier transform infrared spectroscopy and X-ray diffraction analyses revealed the crystals to be ACC, and de novo biomineralization was confirmed by following the incorporation of Sr into calcium carbonate. Our results demonstrate the ability of mantle cells to perform fundamental biomineralization processes via amorphous calcium carbonate, and these cells may be directly involved in pearl oyster shell formation.

  2. Precipitation of calcium carbonate from a calcium acetate and ammonium carbamate batch system

    Science.gov (United States)

    Prah, J.; Maček, J.; Dražič, G.

    2011-06-01

    In this paper, we report a novel approach for preparing precipitated calcium carbonate using solutions of ammonium carbamate and calcium acetate as the sources of calcium and carbon dioxide, respectively. Two different concentrations of the starting solutions at three different temperatures (15, 25 and 50 °C) were used for the reaction. The influence of temperature and concentration on the polymorphism and the resulting morphology of calcium carbonate are discussed. The most important parameter for controlling a particular crystal structure and precipitate morphology were the concentrations of the initial solutions. When initial solutions with lower concentrations were used, the crystal form of the precipitate changed with time. Regardless the different polymorphism at different temperatures, after one day only the calcite form was detected in all samples, regardless of at which temperature the samples were prepared. At higher concentrations, pure vaterite or a mixture of vaterite and calcite were present at the beginning of the experiment. After one day, pure vaterite was found in the samples that were prepared at 15 and 25 °C. If calcium carbonate precipitated at 50 °C, the XRD results showed a mixture of calcite and vaterite regardless of the time at which the sample was taken. The morphology of calcium carbonate particles prepared at various conditions changed from calcite cubes to spherical particles of vaterite and aragonite needles. When a low starting concentration was used, the morphology at the initial stage was strongly affected by the temperature at which the experiments were conducted. However, after one day only, cubes were present in all cases at low initial concentrations. In contrast, at high concentrations spherical particles precipitated at all three temperatures at the beginning of the reaction. Spherical particles were made up from smaller particles. Over time, the size of the particles was diminishing due to their disintegration into

  3. Efifciency of Concrete Crack-healing based on Biological Carbonate Precipitation

    Institute of Scientific and Technical Information of China (English)

    LUO Mian; QIAN Chunxiang; LI Ruiyang; RONG Hui

    2015-01-01

    The aim of this study was to improve the capacity for crack-repair in concrete by developing a new way. The self-healing agent based on biological carbonate precipitation was developed. Crack-healing capacity of the cement paste specimens with this biochemical agent was researched. Scanning electron microscopy (SEM) and X-ray diffraction (XRD) were used to characterize the precipitation in cracks. The healing efficiency was evaluated by measuring the water permeability after crack healing as well.The experimental results show that the applied biochemical agent can successfully improve the self-healing capacity of the cement paste specimens as larger cracks can be healed. The cracks with a width of 0.48 mm in the specimens with the biochemical agent are nearly fully healed by the precipitation after 80d repair. SEM and XRD analysis results demonstrate that the white precipitation in cracks is calcium carbonate, which displays spherical crystal morphology. Meanwhile, the water permeability test result shows that the biochemical agent can significantly decrease the water permeability of the cement paste specimens, the water permeability of specimens with the biochemical agent respectively decreases by 84%and 96%after 7 d and 28 d immersion in water, however the control specimens only respectively decrease by 41%and 60%, which indicates that the bacteria-based concrete appears to be a promising approach to increase concrete durability.

  4. Multiyear precipitation reduction strongly decreases carbon uptake over northern China

    Science.gov (United States)

    Yuan, Wenping; Liu, Dan; Dong, Wenjie; Liu, Shuguang; Zhou, Guangsheng; Yu, Guirui; Zhao, Tianbao; Feng, Jinming; Ma, Zhuguo; Chen, Jiquan; Chen, Yang; Chen, Shiping; Han, Shijie; Huang, Jianping; Li, Linghao; Liu, Huizhi; Liu, Shaoming; Ma, Mingguo; Wang, Yanfeng; Xia, Jiangzhou; Xu, Wenfang; Zhang, Qiang; Zhao, Xinquang; Zhao, Liang

    2014-05-01

    Drought has been a concern in global and regional water, carbon, and energy cycles. From 1999 to 2011, northern China experienced a multiyear precipitation reduction that significantly decreased water availability as indicated by the Palmer Drought Severity Index and soil moisture measurements. In this study, a light use efficiency model (EC-LUE) and an ecosystem physiological model (IBIS) were used to characterize the impacts of long-term drought on terrestrial carbon fluxes in northern China. EC-LUE and IBIS models showed the reduction of averaged GPP of 0.09 and 0.05 Pg C yr-1 during 1999-2011 compared with 1982-1998. Based on the IBIS model, simulated ecosystem respiration experienced an insignificant decrease from 1999 to 2011. The multiyear precipitation reduction changed the regional carbon uptake of 0.011 Pg C yr-1 from 1982 to 1998 to a net source of 0.018 Pg C yr-1 from 1999 to 2011. Moreover, a pronounced decrease in maize yield in almost all provinces in the study region was found from 1999 to 2011 versus the average of yield from1978 to 2011. The largest maize yield reduction occurred in Beijing (2499 kg ha-1 yr-1), Jilin (2180 kg ha-1 yr-1), Tianjing (1923 kg ha-1 yr-1), and Heilongjiang (1791 kg ha-1 yr-1), and the maize yield anomaly was significantly correlated with the annual precipitation over the entire study area. Our results revealed that recent climate change, especially drought-induced water stress, is the dominant cause of the reduction in the terrestrial carbon sink over northern China.

  5. Precipitation of Co(2+) carbonates from aqueous solution: insights on the amorphous to crystalline transformation.

    Science.gov (United States)

    González-López, Jorge; Fernández-González, Ángeles; Jiménez, Amalia

    2016-04-01

    water content. It was surprising the low solubility product (Ksp) of the new phase Co2CO3(OH)2 in the order of 10-30 and this could explain its appearance only after 7 days of aging. On the other hand, the high solubility product of amorphous is consistent with its instantaneous precipitation at the beginning of the reaction. Solution calorimetry shows a higher value of exothermic solution enthalpy for crystalline cobalt hydroxide carbonate and hence, the solubility result are confirmed. Although geochemical models indicated that aqueous solution was supersaturated with respect both phases, the sequence of obtained phases (first amorphous and next crystalline) indicate that the evolution of the saturation index has to be dropped with respect to amorphous phase with time. These results points towards a simultaneous dissolution of the amorphous and the precipitation of crystalline phase Co2CO3(OH)2 at the first stages of the reaction. González-López, J. ; Fernández-González, Á. ; Jiménez, A. (2015) Prepublication: Crystallization of nanostructured cobalt hydroxide carbonate at ambient conditions: a key precursor of Co3O4. DOI: http://dx.doi.org/10.1180/minmag.2015.079.7.02

  6. Diffusion-reaction compromise the polymorphs of precipitated calcium carbonate

    Institute of Scientific and Technical Information of China (English)

    Han Wang; Wenlai Huang; Yongsheng Han

    2013-01-01

    Diffusion is seldom considered by chemists and materialists in the preparation of materials while it plays an important role in the field of chemical engineering.If we look at crystallization at the atomic level,crystal growth in a solution starts from the diffusion of ions to the growing surface followed by the incorporation of ions into its lattice.Diffusion can be a rate determining step for the growth of crystals.In this paper,we take the crystallization of calcium carbonate as an example to illustrate the microscopic processes of diffusion and reaction and their compromising influence on the morphology of the crystals produced.The diffusion effect is studied in a specially designed three-cell reactor.Experiments show that a decrease of diffusion leads to retardation of supersaturation and the formation of a continuous concentration gradient in the reaction cell,thus promoting the formation of cubic calcite particles.The reaction rate is regulated by temperature.Increase of reaction rate favors the formation of needle-like aragonite particles.When diffusion and reaction play joint roles in the reaction system,their compromise dominates the formation of products,leading to a mixture of cubic and needle-like particles with a controllable ratio.Since diffusion and reaction are universal factors in the preparation of materials,the finding of this paper could be helpful in the controlled synthesis of other materials.

  7. Characterization of precipitates in a niobium-zirconium-carbon alloy

    Science.gov (United States)

    Grobstein, T. L.; Titran, R. H.

    1986-01-01

    A niobium alloy with 1 percent zirconium and 0.063 percent carbon by weight was investigated in the as-rolled and annealed conditions, and after high-temperature (1350 and 1400 K) exposure with and without an applied stress. In the as-rolled and annealed conditions, large metastable carbides were observed in addition to a regular distribution of small particles. During the high-temperature exposure, the majority of the large carbides were dissolved and a more stable carbide phase formed. This finely dispersed phase had a composition determined to be approximately 70 percent ZrC and approximately 30 percent NbC and showed some evidence of an orientation relationship with the matrix. The precipitates appeared to coarsen slightly after approximately 5000 hr exposure in the presence of an applied stress resulted in a decrease in the size and in the interparticle spacing of the stable precipitates. However, the composition of the precipitate phase and its ability to pin dislocations were not affected by the temperature or stress conditions.

  8. Carbon Nanoparticles in Nematic Liquid Crystals

    Institute of Scientific and Technical Information of China (English)

    S.Eren San; Mustafa Okutan; O(g)uz K(o)ysal; Yusuf Yer-li

    2008-01-01

    Fullerene G60,C70,single-walled and multi-walled carbon nanotubes and graphene sheets are doped to nematic liquid crystal(LC)host in the same percentage.Planar samples of these mixtures are prepared and our measurements constitute an optimization basis for possible applications.Fullerene balls are found to be the best compatible material for optical aims and reorientation of LC molecules,while the carbon nanotubes experience some reorientation possibility in LC media and graphene layers are good barriers to preserve reorientation.

  9. Enhancing the Effectiveness of Carbon Dioxide Flooding by Managing Asphaltene Precipitation

    Energy Technology Data Exchange (ETDEWEB)

    Deo, Milind D.

    2002-02-21

    Objectives of this project was to understand asphaltene precipitation in General and carbon dioxide induced precipitation in particular. To this effect, thermodynamic and kinetic experiments with the Rangely crude oil were conducted and thermodynamic and reservoir models were developed.

  10. Model of phosphorus precipitation and crystal formation in electric arc furnace steel slag filters.

    Science.gov (United States)

    Claveau-Mallet, Dominique; Wallace, Scott; Comeau, Yves

    2012-02-01

    The objective of this study was to develop a phosphorus retention mechanisms model based on precipitation and crystallization in electric arc furnace slag filters. Three slag columns were fed during 30 to 630 days with a reconstituted mining effluent at different void hydraulic retention times. Precipitates formed in columns were characterized by X-ray diffraction and transmission electronic microscopy. The proposed model is expressed in the following steps: (1) the rate limiting dissolution of slag is represented by the dissolution of CaO, (2) a high pH in the slag filter results in phosphorus precipitation and crystal growth, (3) crystal retention takes place by filtration, settling and growth densification, (4) the decrease in available reaction volume is caused by crystal and other particulate matter accumulation (and decrease in available reaction time), and (5) the pH decreases in the filter over time if the reaction time is too low (which results in a reduced removal efficiency). Crystal organization in a slag filter determines its phosphorus retention capacity. Supersaturation and water velocity affect crystal organization. A compact crystal organization enhances the phosphorus retention capacity of the filter. A new approach to define filter performance is proposed: saturation retention capacity is expressed in units of mg P/mL voids.

  11. Crystallization behaviour of hydroxide cobalt carbonates by aging: Environmental implications.

    Science.gov (United States)

    González-López, Jorge; Fernández-González, Angeles; Jimenez, Amalia

    2014-05-01

    Cobalt is a naturally occurring element widely distributed in water, sediments and air that is essential for living species, since it is a component of B12 vitamin and it is also a strategic and critical element used in a number of commercial, industrial and military applications. However, relatively high accumulations of cobalt in environment can be toxic for human and animal health. Cobalt usually occurs as Co2+ and Co3+ in aqueous solutions, where Co2+ is the most soluble and hence its mobility in water is higher. The study of the precipitation of cobalt carbonates is of great interest due to the abundance of carbonate minerals in contact with surface water and groundwater which can be polluted with Co2+. Previous works have demonstrated that the formation of Co-bearing calcium carbonates and Co-rich low crystallinity phases takes place at ambient conditions. With the aim of investigating the crystallization behavior of Co- bearing carbonates at ambient temperature, macroscopic batch-type experiments have been carried out by mixing aqueous solutions of CoCl2 (0.05M) and Na2CO3 (0.05M) during increasing reaction times (5 minutes and 1, 5, 24, 48, 96, 168, 720 and 1440 hours). The main goals of this work were (i) to analyse the physicochemical evolution of the system and (ii) to study the evolution of the crystallinity of the solid phases during aging. After a given reaction period, pH, alkalinity and dissolved Co2+ in the aqueous solutions were analysed. The evolution of the morphology and chemical composition of the solids with aging time was examined by SEM and TEM. The precipitates were also analyzed by X-ray powder diffraction (XRD) and the crystallinity degree was followed by the intensity and the full width at high medium (FWHM) of the main peaks. The results show that a low crystallinity phase was obtained at the very beginning of aging. This phase evolves progressively to form hydroxide carbonate cobalt (Co2CO3(OH)2) which crystallize with the spatial

  12. From Carbon Nanotube Crystals to Carbon Nanotube Flowers

    Institute of Scientific and Technical Information of China (English)

    ZHANG Zhengjun; ZHAO Ye; ZHOU Ya

    2005-01-01

    We have investigated the very initial deposition stages of chemical vapor deposition (CVD) with ferrocene (Fe(C5H5)2) and xylene (C8H10) for growing carbon nanotubes, and made clear that the mechanism for the self-organization behaviors of nanotubes at different growth stages by this approach. For instance, the organization of nanotubes into flower-like structures at prolonged deposition is developed from the crystal-like structures formed at early growth stages, both of which are closely related to and determined by the very initial deposition stages of this CVD approach. Based on this approach, ways have been established to build up different architectures of carbon nanotubes, by controlling the initial deposition stages of the CVD process, with which we have realized the selective growth of self-organized carbon nanotube structures. This study provides a new idea for growing carbon nanotube architectures by CVD.

  13. Effect of silk sericin on morphology and structure of calcium carbonate crystal

    Science.gov (United States)

    Zhao, Rui-Bo; Han, Hua-Feng; Ding, Shao; Li, Ze-Hao; Kong, Xiang-Dong

    2013-06-01

    In this paper, silk sericin was employed to regulate the mineralization of calcium carbonate (CaCO3). CaCO3 composite particles were prepared by the precipitation reaction of sodium carbonate with calcium chloride solution in the presence of silk sericin. The as-prepared samples were collected at different reaction time to study the crystallization process of CaCO3 by scanning electron microscopy (SEM), Fourier transform infrared spectroscopy (FTIR), thermogravimetric analysis (TGA) and X-ray diffraction (XRD). The results showed that silk sericin significantly affected the morphology and crystallographic polymorph of CaCO3. With increasing the reaction time, the crystal phase of CaCO3 transferred from calcite dominated to vaterite dominated mixtures, while the morphology of CaCO3 changed from disk-like calcite crystal to spherical vaterite crystal. These studies showed the potential of silk sericin used as a template molecule to control the growth of inorganic crystal.

  14. Mechanism of calcium phosphates precipitation in liquid crystals; Mecanisme de precipitation de phosphates de calcium dans des cristaux liquides

    Energy Technology Data Exchange (ETDEWEB)

    Prelot, B.; Zemb, T

    2004-04-01

    The possibility of using as a precursor an easily wet meso-porous powder would be a breakthrough in the preparation of nuclear waste storage ceramics. A concentrated solution containing ions to be stored would wet a dry powder and then, subjected to mild compression, lead to a micro-crystalline matrix of calcium phosphate at acceptable temperatures. Since no porous calcium phosphate different from calcined bone (patented) is described as porous precursor, we have compared the different synthesis routes towards meso-porous ceramics. First, we considered homogeneous precipitation of slats in water: using initially off-stoichiometry in reaction, micron-sized hydroxyapatite particles are produced with a specific surface up to 100 m{sup 2}/g. Then, we consider the classical route of precipitation of an hybrid material in the miscibility gap of a phase diagram, when an hexagonal liquid crystal is used a matrix for precipitation. The surfactant family consists in single chain surfactants containing phosphates as head-group to poison the growing surface of calcium phosphate nano-domains. Since the reaction is still too brutal, we considered using a cat-anionic precursor material of controllable surface charge. For certain concentrations and molar ratios, a new structure not yet described in surfactant precipitation literature is observed: since the periodicity is lower than twice the chain length, a disordered constant curvature monolayer (instead of the classical cylinder of twice chain length diameter) of surfactant is implied. Finally, we have investigated synthesis routes implying slow dissolution of pre-formed calcium phosphate in an already existing hexagonal matrix. For all these routes of synthesis, micro-structural determinations using SAXS, WARS and BET are performed, with a special attention to comparison of the precipitation material, the matrix obtained with all elements present, and also the material obtained after calcinations. (authors)

  15. Carbonate precipitation by the thermophilic archaeon Archaeoglobus fulgidus: a model of carbon flow for an ancient microorganism

    Directory of Open Access Journals (Sweden)

    P. Ostrom

    2008-08-01

    Full Text Available Microbial carbonate precipitation experiments were conducted using the archaeon bacteria Archaeoglobus fulgidus to determine chemical and isotopic fractionation of organic and inorganic carbon into mineral phases. Carbonate precipitation was induced in two different experiments using A. fulgidus to determine the relative abundance of organically derived carbon incorporated into carbonate minerals as well as to define any distinct phases or patterns that could be attributed to the precipitation process. One experiment used a medium containing 13C-depleted organic carbon and 13C-enriched inorganic carbon, and the other used a 14C-labeled organic carbon source. Results indicated that 0.9–24.8% organic carbon was incorporated into carbonates precipitated by A. fulgidus and that this process was mediated primarily by pH and CO2 emission from cells. Data showed that the carbon in the CO2 produced from this microorganism is incorporated into carbonates and that the rate at which precipitation occurs and the dynamics of the carbonate precipitation process are strongly mediated by the specific steps involved in the biochemical process for lactate oxidation by A. fulgidus.

  16. Elucidating the Effect of Biomolecule Structure on Calcium Carbonate Crystal Formation

    Science.gov (United States)

    Kulbok, K. E.; Duckworth, O.

    2011-12-01

    Anthropogenic emissions of carbon dioxide have lead to a steady increase in atmospheric concentration. This greenhouse gas has been identified as a key driver of climate change and also has lead to increased acidification of marine and terrestrial waters. Calcium carbonate precipitation at the Earth's surface is an integral linkage in the global carbon cycle, especially in regards to regulating atmospheric carbon dioxide. As concern for the effect of increasing atmospheric CO2 levels grows, the need to understand calcium carbonate systems escalates concurrently. Calcium carbonate phases are the most abundant group of biominerals; therefore, elucidating the mechanism of biomineralization is critical to understanding CaCO3 precipitation and may aid in the development of novel carbon sequestration strategies. The ubiquity of microorganisms leads to an extensive number of biomolecules present in the Earth's systems, and thus an extensive range of possible effects on CaCO3 formation. Carboxylic acids are very common biomolecules and have a relatively simple structure, thus making them an ideal family of model compounds. This study examines the kinetics, thermodynamics, phase, and morphology of calcium carbonate crystals precipitated in the presence of carboxylate-containing biomolecules, including citric acid, succinic acid, and aspartic acid. The experiments utilize a unique (NH4)2CO3 gas-diffusion reactor, which allows in-situ measurements of chemical conditions during the precipitation and growth of crystals. Continuous monitoring of the in-situ conditions of pCO2, pH, [Ca2+], and optical absorbance provides data on the supersaturation at which nucleation occurs and the kinetics of mineral growth. The use of scanning electron microscopy and X-ray diffraction provides information on the morphology and mineralogy of precipitates. The combination of these data sets will provide an in-depth view of the ideal concentration of calcium ions required for solution saturation

  17. Small angle neutron scattering (SANS) study of γ' precipitates in single crystals of AM1 superalloy

    Science.gov (United States)

    Bellet, D.; Bastie, P.; Royer, A.; Lajzerowicz, J.; Legrand, J. F.; Bonnet, R.

    1992-06-01

    The morphology of γ' precipitates of AM1 single crystal superalloys has been studied by small neutron scattering (SANS), and electron microscopy. Due to the single crystal nature of the samples, the SANS patterns are anisotropic and exhibit a fourfold symmetry corresponding both to the shape and to the spatial arrangement of the precipitates in a (001) plane. Measurements for other sample orientations have allowed us to improve the analysis of the shape of the precipitates. After creep deformation along the axis, a twofold symmetry corresponding to the “rafting” of the γ' precipitates is observed in the (010) plane. The main effect of heat treatments at 1 050 °C, commonly used for industrial applications, is the coarsening of the precipitates. From the displacement of the correlation peaks towards smaller angles, we deduce an average centre-to-centre spacing between the precipitates which increases with the annealing time from 0.3 μm to 0.6 μm according to the Lifshitz, Slyosov, Wagner behaviour. The results are compared to electron microscopy measurements, performed on the same samples.

  18. High-molecular-weight polymers for protein crystallization: poly-γ-glutamic acid-based precipitants

    International Nuclear Information System (INIS)

    High-molecular-weight poly-γ-glutamic acid-based polymers have been synthesized, tested and adopted for protein crystallization. Protein crystallization has been revolutionized by the introduction of high-throughput technologies, which have led to a speeding up of the process while simultaneously reducing the amount of protein sample necessary. Nonetheless, the chemistry dimension of protein crystallization has remained relatively undeveloped. Most crystallization screens are based on the same set of precipitants. To address this shortcoming, the development of new protein precipitants based on poly-γ-glutamic acid (PGA) polymers with different molecular-weight ranges is reported here: PGA-LM (low molecular weight) of ∼400 kDa and PGA-HM (high molecular weight) of >1000 kDa. It is also demonstrated that protein precipitants can be expanded further to polymers with much higher molecular weight than those that are currently in use. Furthermore, the modification of PGA-like polymers by covalent attachments of glucosamine substantially improved their solubility without affecting their crystallization properties. Some preliminary PGA-based screens are presented here

  19. Co-precipitation of dissolved organic matter by calcium carbonate in Pyramid Lake, Nevada

    Science.gov (United States)

    Leenheer, Jerry A.; Reddy, Michael M.

    2008-01-01

    Our previous research has demonstrated that dissolved organic matter (DOM) influences calcium carbonate mineral formation in surface and ground water. To better understand DOM mediation of carbonate precipitation and DOM co-precipitation and/or incorporation with carbonate minerals, we characterized the content and speciation of DOM in carbonate minerals and in the lake water of Pyramid Lake, Nevada, USA. A 400-gram block of precipitated calcium carbonate from the Pyramid Lake shore was dissolved in 8 liters of 10% acetic acid. Particulate matter not dissolved by acetic acid was removed by centrifugation. DOM from the carbonate rock was fractionated into nine portions using evaporation, dialysis, resin adsorption, and selective precipitations to remove acetic acid and inorganic constituents. The calcium carbonate rock contained 0.23% DOM by weight. This DOM was enriched in polycarboxylic proteinaceous acids and hydroxy-acids in comparison with the present lake water. DOM in lake water was composed of aliphatic, alicyclic polycarboxylic acids. These compound classes were found in previous studies to inhibit calcium carbonate precipitation. DOM fractions from the carbonate rock were 14C-age dated at about 3,100 to 3,500 years before present. The mechanism of DOM co-precipitation and/or physical incorporation in the calcium carbonate is believed to be due to formation of insoluble calcium complexes with polycarboxylic proteinaceous acids and hydroxy-acids that have moderately large stability constants at the alkaline pH of the lake. DOM co-precipitation with calcium carbonate and incorporation in precipitated carbonate minerals removes proteinaceous DOM, but nearly equivalent concentrations of neutral and acidic forms of organic nitrogen in DOM remain in solution. Calcium carbonate precipitation during lime softening pretreatment of drinking water may have practical applications for removal of proteinaceous disinfection by-product precursors.

  20. Identifying appropriate conditions for producing spindle-like causticizing precipitated calcium carbonate for paper filler applications

    Directory of Open Access Journals (Sweden)

    Jin Wang

    2012-11-01

    Full Text Available Causticizing precipitated calcium carbonate (CPCC as a by-product of the green liquor causticizing process can be used as paper filler to save resources and reduce costs. In this study, CPCC was prepared with green liquor and quicklime, which were obtained from an alkali recovery line of a paper mill. The factors influencing crystal morphology of CPCC, such as slaking temperature, slaking time, and causticizing time were investigated. The morphology of CPCC was observed and analyzed for optimizing reaction conditions. The following were compared: properties of CPCC obtained in this study, conventional CPCC (white mud from a paper mill, and commercial PCC as fillers. The results showed that slaking time and causticizing time were important for morphology control. Spindle-like and rod-like CPCC obtained in this study had better drainability and retention, higher paper bulk, opacity, and physical strength compared to conventional CPCC, and had nearly the same performances as commercial PCC.

  1. Selective Precipitation and Concentrating of Perovskite Crystals from Titanium-Bearing Slag Melt in Supergravity Field

    Science.gov (United States)

    Gao, Jintao; Zhong, Yiwei; Guo, Zhancheng

    2016-08-01

    Selective precipitation and concentrating of perovskite crystals from titanium-bearing slag melt in the supergravity field was investigated in this study. Since perovskite was the first precipitated phase from the slag melt during the cooling process, and a greater precipitation quantity and larger crystal sizes of perovskite were obtained at 1593 K to 1563 K (1320 °C to 1290 °C), concentrating of perovskite crystals from the slag melt was carried out at this temperature range in the supergravity field, at which the perovskite transforms into solid particles while the other minerals remain in the liquid melt. The layered structures appeared significantly in the sample obtained by supergravity treatment, and all the perovskite crystals moved along the supergravity direction and concentrated as the perovskite-rich phase in the bottom area, whereas the molten slag concentrated in the upper area along the opposite direction, in which it was impossible to find any perovskite crystals. With the gravity coefficient of G = 750, the mass fraction of TiO2 in the perovskite-rich phase was up to 34.65 wt pct, whereas that of the slag phase was decreased to 12.23 wt pct, and the recovery ratio of Ti in the perovskite-rich phase was up to 75.28 pct. On this basis, an amplification experimental centrifugal apparatus was exploited and the continuous experiment with larger scale was further carried out, the results confirming that selective precipitation and concentrating of perovskite crystals from the titanium-bearing slag melt by supergravity was a feasible method.

  2. Calcium Carbonate Precipitation by Bacillus and Sporosarcina Strains Isolated from Concrete and Analysis of the Bacterial Community of Concrete.

    Science.gov (United States)

    Kim, Hyun Jung; Eom, Hyo Jung; Park, Chulwoo; Jung, Jaejoon; Shin, Bora; Kim, Wook; Chung, Namhyun; Choi, In-Geol; Park, Woojun

    2016-03-01

    Microbially induced calcium carbonate precipitation (CCP) is a long-standing but re-emerging environmental engineering process for production of self-healing concrete, bioremediation, and long-term storage of CO2. CCP-capable bacteria, two Bacillus strains (JH3 and JH7) and one Sporosarcina strain (HYO08), were isolated from two samples of concrete and characterized phylogenetically. Calcium carbonate crystals precipitated by the three strains were morphologically distinct according to field emission scanning electron microscopy. Energy dispersive X-ray spectrometry mapping confirmed biomineralization via extracellular calcium carbonate production. The three strains differed in their physiological characteristics: growth at alkali pH and high NaCl concentrations, and urease activity. Sporosarcina sp. HYO08 and Bacillus sp. JH7 were more alkali- and halotolerant, respectively. Analysis of the community from the same concrete samples using barcoded pyrosequencing revealed that the relative abundance of Bacillus and Sporosarcina species was low, which indicated low culturability of other dominant bacteria. This study suggests that calcium carbonate crystals with different properties can be produced by various CCP-capable strains, and other novel isolates await discovery. PMID:26699752

  3. Calcium Carbonate Precipitation by Bacillus and Sporosarcina Strains Isolated from Concrete and Analysis of the Bacterial Community of Concrete.

    Science.gov (United States)

    Kim, Hyun Jung; Eom, Hyo Jung; Park, Chulwoo; Jung, Jaejoon; Shin, Bora; Kim, Wook; Chung, Namhyun; Choi, In-Geol; Park, Woojun

    2016-03-01

    Microbially induced calcium carbonate precipitation (CCP) is a long-standing but re-emerging environmental engineering process for production of self-healing concrete, bioremediation, and long-term storage of CO2. CCP-capable bacteria, two Bacillus strains (JH3 and JH7) and one Sporosarcina strain (HYO08), were isolated from two samples of concrete and characterized phylogenetically. Calcium carbonate crystals precipitated by the three strains were morphologically distinct according to field emission scanning electron microscopy. Energy dispersive X-ray spectrometry mapping confirmed biomineralization via extracellular calcium carbonate production. The three strains differed in their physiological characteristics: growth at alkali pH and high NaCl concentrations, and urease activity. Sporosarcina sp. HYO08 and Bacillus sp. JH7 were more alkali- and halotolerant, respectively. Analysis of the community from the same concrete samples using barcoded pyrosequencing revealed that the relative abundance of Bacillus and Sporosarcina species was low, which indicated low culturability of other dominant bacteria. This study suggests that calcium carbonate crystals with different properties can be produced by various CCP-capable strains, and other novel isolates await discovery.

  4. STEREOREGULAR POLY(CYCLOHEXENE CARBONATE)S: UNIQUE CRYSTALLIZATION BEHAVIOR

    Institute of Scientific and Technical Information of China (English)

    Guang-peng Wu; Shi-dong Jiang; Xiao-bing Lu; Wei-min Ren; Shou-ke Yan

    2012-01-01

    An example of crystalline CO2-based polymer from the asymmetric alternating copolymerization of CO2 and cyclohexene oxide is reported.Isotacticity of poly(cyclohexene carbonate) (PCHC) has the critical influence on the crystallinity,and only copolymers with a isotacticity of more than 90% are crystallizable.The stereoregular PCHC is a typical semi-crystalline thermoplastic,and possesses a high melting point (Tm) of 215-230℃ and a decomposition temperature of ca.310℃.The spherulitic morphology of (R)-PCHC grows in a clockwise spiral from a center,and that of (S)-PCHC is a counterclockwise spiral,while the stereocomplex of (S)-PCHC/(R)-PCHC (1/1 mass ratio) presents lath-like dendritic crystal.The novel crystalline CO2-based polycarbonate represents a rare example of optically active polymers with unique crystallization behavior.Our findings reflect the critical influence of stereoregularity on the crystallization for this kind of polymeric materials,and may lead to developments of thermal-resistance CO2 copolymers for application in engineering thermoplastics.

  5. Study of precipitated phases in Mn2+ singly doped KBr crystals by optical spectroscopy and EPR

    International Nuclear Information System (INIS)

    The aggregation states of Mn2+ in KBr:Mn2+ doped crystals are investigated using optical techniques. Excitation and luminescence spectra as well as lifetimes are obtained as a function of temperature of different crystals. It is demonstrated that at least three different Mn2+ precipitates are formed inside the KBr. Two of them contain MnBr64- units with slightly distorted octahedral symmetries, while the third one involves two non-equivalent tetrahedral MnBr42- units. These centers exhibit a broad green luminescence band. (orig.)

  6. Kinetics of crystal growth on seeded precipitation of sodium aluminate solutions with new device

    Institute of Scientific and Technical Information of China (English)

    陈金清; 张平民; 甘国耀; 尹周澜; 陈启元

    2004-01-01

    A new device was designed, which can effectively avoid the undesired nucleation and agglomeration of fine particles on the experimental results during the seaded precipitation of sodium aluminate solution, and moreover, the experimental conditions are nearly kept constant during the experiment. With the new device, it is proven that a good result can be obtained on the kinetics study of the crystal growth in seeded precipitation of sodium aluminate solution. Experiments were carried out with the concentration of Na2 O (Nk)170 g/L, the mole ratio of Na2 O to Al2 O3 (αk) all between 1.52 to 2.01, at 65, 70, 75 ℃, respectively. And the kinetics equation of crystal growth of gibbsite was deduced.

  7. Carbonate precipitation through microbial activities in natural environment, and their potential in biotechnology: a review

    Directory of Open Access Journals (Sweden)

    Tingting eZhu

    2016-01-01

    Full Text Available Calcium carbonate represents a large portion of carbon reservoir and is used commercially for a variety of applications. Microbial carbonate precipitation (MCP, a by-product of microbial activities, plays an important metal coprecipitation and cementation role in natural systems. This natural process occurring in various geological settings can be mimicked and used for a number of biotechnology such as metal remediation, carbon sequestration, enhanced oil recovery and construction restoration. In this study, different metabolic activities leading to calcium carbonate precipitation, their native environment, and potential applications and challenges are reviewed.

  8. Exploring Carbon Nanomaterial Diversity for Nucleation of Protein Crystals

    OpenAIRE

    Lata Govada; Hannah S. Leese; Emmanuel Saridakis; Sean Kassen; Benny Chain; Sahir Khurshid; Robert Menzel; Sheng Hu; Shaffer, Milo S. P.; Chayen, Naomi E.

    2016-01-01

    Controlling crystal nucleation is a crucial step in obtaining high quality protein crystals for structure determination by X-ray crystallography. Carbon nanomaterials (CNMs) including carbon nanotubes, graphene oxide, and carbon black provide a range of surface topographies, porosities and length scales; functionalisation with two different approaches, gas phase radical grafting and liquid phase reductive grafting, provide routes to a range of oligomer functionalised products. These grafted m...

  9. GFP facilitates native purification of recombinant perlucin derivatives and delays the precipitation of calcium carbonate.

    Directory of Open Access Journals (Sweden)

    Eva Weber

    Full Text Available Insolubility is one of the possible functions of proteins involved in biomineralization, which often limits their native purification. This becomes a major problem especially when recombinant expression systems are required to obtain larger amounts. For example, the mollusc shell provides a rich source of unconventional proteins, which can interfere in manifold ways with different mineral phases and interfaces. Therefore, the relevance of such proteins for biotechnological processes is still in its infancy. Here we report a simple and reproducible purification procedure for a GFP-tagged lectin involved in biomineralization, originally isolated from mother-of-pearl in abalone shells. An optimization of E. coli host cell culture conditions was the key to obtain reasonable yields and high degrees of purity by using simple one-step affinity chromatography. We identified a dual functional role for the GFP domain when it became part of a mineralizing system in vitro. First, the GFP domain improved the solubility of an otherwise insoluble protein, in this case recombinant perlucin derivatives. Second, GFP inhibited calcium carbonate precipitation in a concentration dependent manner. This was demonstrated here using a simple bulk assay over a time period of 400 seconds. At concentrations of 2 µg/ml and higher, the inhibitory effect was observed predominantly for HCO(3 (- as the first ionic interaction partner, but not necessarily for Ca(2+. The interference of GFP-tagged perlucin derivatives with the precipitation of calcium carbonate generated different types of GFP-fluorescent composite calcite crystals. GFP-tagging offers therefore a genetically tunable tool to gently modify mechanical and optical properties of synthetic biocomposite minerals.

  10. Enhancing the Effectiveness of Carbon Dioxide Flooding by Managing Asphaltene Precipitation

    Energy Technology Data Exchange (ETDEWEB)

    Deo, M.D.

    2001-01-12

    The objective of this project was to identify conditions at which carbon dioxide induced precipitation occurred in crude oils. Establishing compositions of the relevant liquid and solid phases was planned. Other goals of the project were to determine if precipitation occurred in cores and to implement thermodynamic and compositional models to examine the phenomenon. Exploring kinetics of precipitation was also one of the project goals. Crude oil from the Rangely Field (eastern Colorado) was used as a prototype.

  11. Deposition of the platinum crystals on the carbon nanotubes

    Institute of Scientific and Technical Information of China (English)

    2000-01-01

    A new technique and the affecting factors for depositing platinum on the carbon nanotubes were investigated. The results show that the deposited platinum crystals in the atmosphere of hydrogen or nitrogen have a small size and a homogeneous distribution on the surface of the carbon nanotubes. The pretreatment would decrease the platinum particles on the carbon nanotubes significantly.

  12. High precipitation rate in a Middle Triassic carbonate platform: Implications on the relationship between seawater saturation state and carbonate production

    Science.gov (United States)

    Franceschi, Marco; Preto, Nereo; Marangon, Alessandro; Gattolin, Giovanni; Meda, Marco

    2016-06-01

    Three-dimensional geological modeling of the Middle Triassic Latemar carbonate platform is coupled with facies modal analysis to estimate its carbonate precipitation rate (G). The 3D model, strongly constrained by field data, encompasses a specific stratigraphic interval of the platform, bounded by two isochronous surfaces. Modal analysis of thin sections allows estimating the proportion of syndepositional vs postdepositional carbonate in the facies associations of the platform. This, together with the 3D facies distribution in the model that takes into account lateral and vertical facies variability, permits to calculate the volumes of syndepositional carbonate preserved at Latemar between the two considered isochrones. Given the peculiar characteristics of the platform, that does not show evidences of strong dissolution processes or large carbonate mass loss through export in the nearby basins, results can be used to estimate the average precipitation rate of the platform in the considered time interval. This estimate allows discussion in relation to models of ocean water saturation state (Ω) with respect to carbonates in the geological past, and comparison to the calculated precipitation rates of modern tropical coral reef ecosystems at global and reef scale. A high G value is found at Latemar and represents the first empirical confirmation that, in the Triassic, extremes in Ω may have triggered high carbonate precipitation in shallow water settings; moreover, comparison to modern reefs points to a possible common relationship that may link seawater Ω and precipitation rate in carbonate platform ecosystems through geological time.

  13. Mass Transfer and Kinetics Study of Heterogeneous Semi-Batch Precipitation of Magnesium Carbonate

    DEFF Research Database (Denmark)

    Han, B.; Qu, H. Y.; Niemi, H.;

    2014-01-01

    Precipitation kinetics and mass transfer of magnesium carbonate (MgCO3) hydrates from a reaction of magnesium hydroxide (Mg(OH)(2)) and CO2 were analyzed. The effect of CO2 flow rate and mixing intensity on precipitation was investigated under ambient temperature and atmospheric pressure. Raman...

  14. Environmental vs microbial control on ca-carbonate precipitation in fluvial tufa (NW Calabria-Italy)

    Science.gov (United States)

    Manzo, E.; Perri, E.; Tucker, M. E.

    2009-04-01

    -shaped lobes and on the upper downstream face of the dams. Vacuolar tufas, which are observable on the upstream surface of the dams, compose the inner part of the dams and the core of the tongue-shaped bodies. Lamination of stromatolitic tufa is almost even and regular with only gentle doming. Laminae, which are 1-2 mm in thickness, originate by the alternation of two main types of microstructure: dendrolitic and detrital layers. Dendrolites, up to 1-1.5 mm thick contain mineralised upward-branching filaments a few micron in diameter, forming bush-likes fans. Filaments coalesce upward to form a solid carbonate layer. Filaments coalesce upwards to form a solid carbonate layer. They are formed by an envelope of micritic crystals of calcite around the sheath of individual cyanobacterial filaments. Detrital layers consist of a minor amount of mineralised cyanobacterial filaments, which appear mainly in transverse section. Carbonate minerals form thin radiating fibrous crystals around the filaments. Micron sized platy crystals of clay minerals and allochthonous dolomitic grains are abundant in such layers. Laminae of stromatolitic tufa also are characterized by the presence of empty tubes, subspherical/lenticular in section, probably originated by insect encrusted larvae. Vacuolar tufas consist of calcified plant remains that contain abundant large voids. Plant leaves, often with a preferred orientation, are the main component, with stems, twigs and mosses. Sub-millimetric carbonate crusts, which form around the plant material, consist of micro-spar fan-shaped calcite crystals 50-100 μm thick. Remains of cyanobacteria filaments, fungal hyphae and diatoms are absent within these calcite crusts, probably since no was biofilm on their external synsedimentary surface. Calcium carbonate tufa precipitation in the Parmenta stream is probably strongly controlled by the calcite supersaturation of the water, since the saturation index is about 0,7. Calcite in vacuolar tufas lacking evidence

  15. Environmental vs microbial control on ca-carbonate precipitation in fluvial tufa (NW Calabria-Italy)

    Science.gov (United States)

    Manzo, E.; Perri, E.; Tucker, M. E.

    2009-04-01

    -shaped lobes and on the upper downstream face of the dams. Vacuolar tufas, which are observable on the upstream surface of the dams, compose the inner part of the dams and the core of the tongue-shaped bodies. Lamination of stromatolitic tufa is almost even and regular with only gentle doming. Laminae, which are 1-2 mm in thickness, originate by the alternation of two main types of microstructure: dendrolitic and detrital layers. Dendrolites, up to 1-1.5 mm thick contain mineralised upward-branching filaments a few micron in diameter, forming bush-likes fans. Filaments coalesce upward to form a solid carbonate layer. Filaments coalesce upwards to form a solid carbonate layer. They are formed by an envelope of micritic crystals of calcite around the sheath of individual cyanobacterial filaments. Detrital layers consist of a minor amount of mineralised cyanobacterial filaments, which appear mainly in transverse section. Carbonate minerals form thin radiating fibrous crystals around the filaments. Micron sized platy crystals of clay minerals and allochthonous dolomitic grains are abundant in such layers. Laminae of stromatolitic tufa also are characterized by the presence of empty tubes, subspherical/lenticular in section, probably originated by insect encrusted larvae. Vacuolar tufas consist of calcified plant remains that contain abundant large voids. Plant leaves, often with a preferred orientation, are the main component, with stems, twigs and mosses. Sub-millimetric carbonate crusts, which form around the plant material, consist of micro-spar fan-shaped calcite crystals 50-100 μm thick. Remains of cyanobacteria filaments, fungal hyphae and diatoms are absent within these calcite crusts, probably since no was biofilm on their external synsedimentary surface. Calcium carbonate tufa precipitation in the Parmenta stream is probably strongly controlled by the calcite supersaturation of the water, since the saturation index is about 0,7. Calcite in vacuolar tufas lacking evidence

  16. Kinetic study of nucleation and crystal growth during oxalic precipitation in the nuclear industry

    International Nuclear Information System (INIS)

    In spite of an extensive use in chemical industry, most of precipitation processes are based on global and empirical knowledge. However, in the recent years, fundamental and phenomenological theories have been developed and they can be used to better understand the mechanisms of precipitation of plutonium IV oxalate, which is a significant stage of the irradiated fuel reprocessing. For this reason, appropriate methods were developed to study nucleation and crystal growth kinetics in a nuclear environment under a wide range of operating conditions. Each phenomena was studied individually in order to reduce the free parameters of the System. This study bears on the oxalates of plutonium and elements which simulate plutonium behaviour during the precipitation, neodymium III and uranium IV. A compact apparatus of a specific construction was used for nucleation measurements in accordance with the Nielsen's method. The state of the mixing was characterised at the reactor scale (macro-mixing) and at molecular scale (micro-mixing). The experimental results for the studied oxalates are in good agreement with the Volmer and Weber's theory. We propose primary nucleation kinetic laws over a wide range of operating conditions (temperature, non-stoichiometric conditions, acidity...). An original method, using a high seed charge, was developed for the determination of crystal growth kinetics, in a batch crystallizer. The crystal growth rate is first order with respect to the supersaturation and the kinetic constant follows an Arrhenius type relation with activation energies of 14, 29 and 36 kJ.mol-1 for respectively neodymium III, uranium IV and plutonium IV oxalates. The overall growth process is surface integration controlled, with a screw dislocation mechanism.

  17. Carbon partitioning during quenching and partitioning heat treatment accompanied by carbide precipitation

    International Nuclear Information System (INIS)

    Carbon partitioning from martensite into austenite in the quenching and partitioning (Q&P) process has been suggested to be controlled by the constrained carbon equilibrium (CCE) criterion. It defines an approach for predicting the carbon concentration in austenite under the condition that competing reactions such as carbide formation and bainite transformation are suppressed. Carbide precipitation in martensite is, however, often observed during the partitioning step, even in low-carbon steels as well as in high-carbon steels, even when containing a high amount of Si. Therefore, carbon partitioning from martensite into austenite is studied here, considering carbide precipitation in martensite. Carbon partitioning was investigated by means of a field-emission electron probe micro analysis (FE-EPMA) and atom probe tomography (APT), using 1.07 wt.% and 0.59 wt.% carbon steels with various martensite volume fractions. Carbon partitioning from martensite to austenite was clearly observed in all specimens, even though a considerable amount of carbide precipitated inside the martensite. The austenite carbon concentration after the partitioning step was not influenced by either the martensite volume fraction or the bulk carbon content. A modified model for predicting the austenite carbon concentration after the partitioning step was proposed to explain the experimental results by assuming carbon equilibria between austenite, ferrite and cementite under a constrained condition

  18. Suppression of tin precipitation in SiSn alloy layers by implanted carbon

    DEFF Research Database (Denmark)

    Gaiduk, Peter; Hansen, John Lundsgaard; Nylandsted Larsen, Arne;

    2014-01-01

    By combining transmission electron microscopy and Rutherford backscattering spectrometry, we have identified carbon related suppression of dislocations and tin precipitation in supersaturated molecular-beam epitaxial grown SiSn alloy layers. Secondary ion mass spectrometry has exposed the accumul......By combining transmission electron microscopy and Rutherford backscattering spectrometry, we have identified carbon related suppression of dislocations and tin precipitation in supersaturated molecular-beam epitaxial grown SiSn alloy layers. Secondary ion mass spectrometry has exposed...

  19. Disordered nano-wrinkle substrates for inducing crystallization over a wide range of concentration of protein and precipitant

    CERN Document Server

    Ghatak, Anindita Sengupta

    2015-01-01

    There are large number of proteins, the existence of which are known but not their crystal structure, because of difficulty in finding the exact condition for their crystallization. Heterogeneous nucleation on disordered porous substrates with small yet large distribution of pores is considered a panacea for this problem, but a universal nucleant, suitable for crystallizing large variety of proteins does not really exist. To this end, we report here a nano-wrinkled substrate which displays remarkable ability and control over protein crystallization. Experiments with different proteins show that on these substrates, crystals nucleate even at very low protein concentration in buffer. Small number of very large crystals appear for precipitant concentrations varied over orders of magnitude ~0.003-0.3M; for some proteins, crystals appear even without addition of any precipitant, not seen with any other heterogeneous substrates. In essence, these substrates significantly diminish the influence of the above two para...

  20. Can Mg isotopes be used to trace cyanobacteria-mediated magnesium carbonate precipitation in alkaline lakes?

    Science.gov (United States)

    Shirokova, L. S.; Mavromatis, V.; Bundeleva, I.; Pokrovsky, O. S.; Bénézeth, P.; Pearce, C.; Gérard, E.; Balor, S.; Oelkers, E. H.

    2011-07-01

    The fractionation of Mg isotopes was determined during the cyanobacterial mediated precipitation of hydrous magnesium carbonate precipitation in both natural environments and in the laboratory. Natural samples were obtained from Lake Salda (SE Turkey), one of the few modern environments on the Earth's surface where hydrous Mg-carbonates are the dominant precipitating minerals. This precipitation was associated with cyanobacterial stromatolites which were abundant in this aquatic ecosystem. Mg isotope analyses were performed on samples of incoming streams, groundwaters, lake waters, stromatolites, and hydromagnesite-rich sediments. Laboratory Mg carbonate precipitation experiments were conducted in the presence of purified Synechococcus sp cyanobacteria that were isolated from the lake water and stromatolites. The hydrous magnesium carbonates nesquehonite (MgCO3·3H2O) and dypingite (Mg5(CO3)4(OH)25(H2O)) were precipitated in these batch reactor experiments from aqueous solutions containing either synthetic NaHCO3/MgCl2 mixtures or natural Lake Salda water, in the presence and absence of live photosynthesizing Synechococcus sp. Bulk precipitation rates were not to affected by the presence of bacteria when air was bubbled through the system. In the stirred non-bubbled reactors, conditions similar to natural settings, bacterial photosynthesis provoked nesquehonite precipitation, whilst no precipitation occurred in bacteria-free systems in the absence of air bubbling, despite the fluids achieving a similar or higher degree of supersaturation. The extent of Mg isotope fractionation (Δ26Mgsolid-solution) between the mineral and solution in the abiotic experiments was found to be identical, within uncertainty, to that measured in cyanobacteria-bearing experiments, and ranges from -1.4 to -0.7 ‰. This similarity refutes the use of Mg isotopes to validate microbial mediated precipitation of hydrous Mg carbonates.

  1. Microbially Accelerated Carbonate Mineral Precipitation as a Strategy for in Situ Carbon Sequestration and Rehabilitation of Asbestos Mine Sites.

    Science.gov (United States)

    McCutcheon, Jenine; Wilson, Siobhan A; Southam, Gordon

    2016-02-01

    A microbially accelerated process for the precipitation of carbonate minerals was implemented in a sample of serpentinite mine tailings collected from the abandoned Woodsreef Asbestos Mine in New South Wales, Australia as a strategy to sequester atmospheric CO2 while also stabilizing the tailings. Tailings were leached using sulfuric acid in reaction columns and subsequently inoculated with an alkalinity-generating cyanobacteria-dominated microbial consortium that was enriched from pit waters at the Woodsreef Mine. Leaching conditions that dissolved 14% of the magnesium from the serpentinite tailings while maintaining circumneutral pH (1800 ppm, pH 6.3) were employed in the experiment. The mineralogy, water chemistry, and microbial colonization of the columns were characterized following the experiment. Micro-X-ray diffraction was used to identify carbonate precipitates as dypingite [Mg5(CO3)4(OH)2·5H2O] and hydromagnesite [Mg5(CO3)4(OH)2·4H2O] with minor nesquehonite (MgCO3·3H2O). Scanning electron microscopy revealed that carbonate mineral precipitates form directly on the filamentous cyanobacteria. These findings demonstrate the ability of these organisms to generate localized supersaturating microenvironments of high concentrations of adsorbed magnesium and photosynthetically generated carbonate ions while also acting as nucleation sites for carbonate precipitation. This study is the first step toward implementing in situ carbon sequestration in serpentinite mine tailings via microbial carbonate precipitation reactions. PMID:26720600

  2. Soil Organic Carbon and Labile Carbon Along a Precipitation Gradient and Their Responses to Some Environmental Changes

    Institute of Scientific and Technical Information of China (English)

    WANG Shu-Ping; ZHOU Guang-Sheng; GAO Su-Hua; GUO Jian-Ping

    2005-01-01

    Based on data from a field survey in 2001 along the Northeast China transect (NECT), a precipitation gradient,and a short-term simulation experiment under ambient CO2 of 350 μmol mol-1 and doubled CO2 of 700 μmol mol-1 with different soil moisture contents of 30%-45%, 45%-60%, and 60%-80% soil water holding capacity, the distribution of soil organic carbon and labile carbon along the NECT, their relationships with precipitation and their responses to CO2 enrichment and soil moisture changes were analyzed. The results indicated that the soil labile carbon along the gradient was significantly related to soil organic carbon (r = 0.993, P < 0.001). The soil labile carbon decreased more rapidly with depth than organic carbon. The soil organic and labile carbon along the gradient decreased with decrease in longitude in both the topsoils and subsoils, and the coefficient of variation for the labile carbon was greater than that for the organic carbon. Both the soil organic carbon and labile carbon had significant linear relationships with precipitation,with the correlation coefficient of soil organic carbon being lower (0.677 at P <0.001) than that of soil labile carbon (0.712 at P < 0.001). In the simulation experiment with doubled and ambient CO2 and different moisture contents, the coefficient of variation for soil organic carbon was only 1.3%, while for soil labile carbon it was 29.7%. With doubled CO2 concentration (700μmol mol-1), soil labile carbon decreased significantly at 45% to 60% of soil moisture content. These indicated that soil labile carbon was relatively more sensitive to environmental changes than soil organic carbon.

  3. Nano-scaled iron-carbon precipitates in HSLC and HSLA steels

    Institute of Scientific and Technical Information of China (English)

    2007-01-01

    This paper studies the composition, quantity and particle size distribution of nano-scaled precipitates with size less than 20 nm in high strength low carbon (HSLC) steel and their effects on mechanical properties of HSLC steel by means of mass balance calculation of nano-scaled precipitates measured by chemical phase analysis plus SAXS method, high-resolution TEM analysis and thermodynamics calculation, as well as temper rapid cooling treatment of ZJ330. It is found that there existed a large quantity of nano-scaled iron-carbon precipitates with size less than 18 nm in low carbon steel produced by CSP and they are mainly Fe-O-C and Fe-Ti-O-C precipitates formed below temperature A1. These precipitates have ob- vious precipitation strengthening effect on HSLC steel and this may be regarded as one of the main reasons why HSLC steel has higher strength. There also existed a lot of iron-carbon precipitates with size less than 36 nm in HSLA steels.

  4. Nano-scaled iron-carbon precipitates in HSLC and HSLA steels

    Institute of Scientific and Technical Information of China (English)

    FU Jie; WU HuaJie; LIU YangChun; KANG YongLin

    2007-01-01

    This paper studies the composition, quantity and particle size distribution of nano-scaled precipitates with size less than 20 nm in high strength Iow carbon (HSLC) steel and their effects on mechanical properties of HSLC steel by means of mass balance calculation of nano-scaled precipitates measured by chemical phase analysis plus SAXS method, high-resolution TEM analysis and thermodynamics calculation, as well as temper rapid cooling treatment of ZJ330. It is found that there existed a large quantity of nano-scaled iron-carbon precipitates with size less than 18 nm in Iow carbon steel produced by CSP and they are mainly Fe-O-C and Fe-Ti-O-C precipitates formed below temperature A1. These precipitates have obvious precipitation strengthening effect on HSLC steel and this may be regarded as one of the main reasons why HSLC steel has higher strength. There also existed a lot of iron-carbon precipitates with size less than 36 nm in HSLA steels.

  5. Preliminary Study On The Precipitation Of Ammonium Carbonate (AUC) From Uranylfluoride (UO2F2) Solution

    International Nuclear Information System (INIS)

    The preliminary studies on the precipitation process of ammonium uranyl carbonate (AUC)-(NH4)4UO2(CO3)3 from the UO2F2-HF solution system by using precipitation agent of ammonium carbonate (AC)-(NH4)2CO3 and on preparation ability of UO2 powder via AUC route are shown in this report. Our analysis results suggested that a product, identified as ammonium uranyl fluoride (AUF), was found along with the AUC precipitate. In order to prevent the formation of the undesirable AUF precipitate, the AUC precipitation process was carried out in the stable pH media ∼ 9, uranium concentration of 100 g/L and molar ratio of C to U ≥ 7.5. (author)

  6. The transient response of global-mean precipitation to increasing carbon dioxide levels

    International Nuclear Information System (INIS)

    The transient response of global-mean precipitation to an increase in atmospheric carbon dioxide levels of 1% yr-1 is investigated in 13 fully coupled atmosphere-ocean general circulation models (AOGCMs) and compared to a period of stabilization. During the period of stabilization, when carbon dioxide levels are held constant at twice their unperturbed level and the climate left to warm, precipitation increases at a rate of ∼ 2.4% per unit of global-mean surface-air-temperature change in the AOGCMs. However, when carbon dioxide levels are increasing, precipitation increases at a smaller rate of ∼ 1.5% per unit of global-mean surface-air-temperature change. This difference can be understood by decomposing the precipitation response into an increase from the response to the global surface-temperature increase (and the climate feedbacks it induces), and a fast atmospheric response to the carbon dioxide radiative forcing that acts to decrease precipitation. According to the multi-model mean, stabilizing atmospheric levels of carbon dioxide would lead to a greater rate of precipitation change per unit of global surface-temperature change.

  7. Enhancement of carbon nanotube photoluminescence by photonic crystal nanocavities

    OpenAIRE

    Watahiki, R.; Shimada, T; Zhao, P; Chiashi, S.; Iwamoto, S.; Arakawa, Y; Maruyama, S.; Kato, Y. K.

    2012-01-01

    Photonic crystal nanocavities are used to enhance photoluminescence from single-walled carbon nanotubes. Micelle-encapsulated nanotubes are deposited on nanocavities within Si photonic crystal slabs and confocal microscopy is used to characterize the devices. Photoluminescence spectra and images reveal nanotube emission coupled to nanocavity modes. The cavity modes can be tuned throughout the emission wavelengths of carbon nanotubes, demonstrating the ability to enhance photoluminescence from...

  8. Enhancement of carbon nanotube photoluminescence by photonic crystal nanocavities

    OpenAIRE

    Watahiki, R.; Shimada, T; Zhao, P; Chiashi, S.; Iwamoto, S.; Arakawa, Y; Maruyama, S.; Kato, Y. K.

    2012-01-01

    Photonic crystal nanocavities are used to enhance photoluminescence from single-walled carbon nanotubes. Micelle-encapsulated nanotubes are deposited on nanocavities within Si photonic crystal slabs and confocal microscopy is used to characterize the devices.Photoluminescencespectra and images reveal nanotube emission coupled to nanocavity modes. The cavity modes can be tuned throughout the emission wavelengths of carbon nanotubes, demonstrating the ability to enhance photoluminescence from a...

  9. Synthesis and crystal kinetics of cerium oxide nanocrystallites prepared by co-precipitation process

    Energy Technology Data Exchange (ETDEWEB)

    Shih, C.J., E-mail: cjshih@kmu.edu.tw [Department of Fragrance and Cosmetics Science, Kaohsiung Medical University, 100 Shi-Chuan 1st Road, Kaohsiung 807, Taiwan (China); Chen, Y.J. [Institute of Biomedical Sciences, National Sun Yat-Sen University, Kaohsiung 804, Taiwan (China); Hon, M.H. [Department of Materials Science and Engineering, National Cheng Kung University, Tainan 701, Taiwan (China)

    2010-05-15

    Cerium oxide nanocrystallites were synthesized at a relatively low temperature using cerium nitrate as starting materials in a water solution by a co-precipitation process. Effect of calcination temperature on the crystallite growth of cerium oxide nano-powders was investigated by X-ray diffraction, transmission electron microscopy and electron diffraction. The crystallization temperature of the cerium oxide powders was estimated to be about 273 K by XRD analysis. When calcined from 473 to 1273 K, the crystallization of the face-centered cubic phase was observed by XRD. The crystallite size of the cerium oxide increased from 10.0 to 43.8 nm with calcining temperature increasing from 673 to 1273 K. The activation energy for growth of cerium oxide nanoparticles was found to be 16.0 kJ mol{sup -1}.

  10. Synthesis and crystal kinetics of cerium oxide nanocrystallites prepared by co-precipitation process

    International Nuclear Information System (INIS)

    Cerium oxide nanocrystallites were synthesized at a relatively low temperature using cerium nitrate as starting materials in a water solution by a co-precipitation process. Effect of calcination temperature on the crystallite growth of cerium oxide nano-powders was investigated by X-ray diffraction, transmission electron microscopy and electron diffraction. The crystallization temperature of the cerium oxide powders was estimated to be about 273 K by XRD analysis. When calcined from 473 to 1273 K, the crystallization of the face-centered cubic phase was observed by XRD. The crystallite size of the cerium oxide increased from 10.0 to 43.8 nm with calcining temperature increasing from 673 to 1273 K. The activation energy for growth of cerium oxide nanoparticles was found to be 16.0 kJ mol-1.

  11. Synthesis of porous carbon balls from spherical colloidal crystal templates.

    Science.gov (United States)

    Kim, Youngchan; Cho, Chang-Yeol; Kang, Ji-Hwan; Cho, Young-Sang; Moon, Jun Hyuk

    2012-07-17

    Spherical inverse opal (IO) porous carbon was produced utilizing silica colloidal crystal spheres as templates. The spherical colloidal crystals were obtained through the self-assembly of monodisperse particles inside an emulsion droplet with confined geometry. The templates were inverted using a carbon precursor, phenol-formaldehyde (PF) resol. We demonstrated a two-step synthesis involving the subsequent infiltration of the PF resol precursor into the spherical colloidal crystal template and a one-step synthesis using a silica colloidal solution containing dissolved PF resol. In the former case, the sizes of the IO carbon balls were controlled by the size of the colloidal crystal templates, and diameters of a few micrometers up to 50 μm were obtained. The average diameter of the macropores created by the silica particles was 230 nm. Moreover, meso-/macroporous IO carbon balls were created using block-copolymer templates in the PF resol. In the one-step synthesis, the concentration of PF resol in the colloidal solution controlled the diameter of the IO carbon balls. IO balls smaller than 3 μm were obtained from the direct addition of 5% PF resol. The one-step synthesis produced rather irregular porous structures reflecting the less ordered crystallization processes inside the spherical colloidal crystals. Nitrogen adsorption and cyclic voltammetry measurements were conducted to measure the specific area and electroactive surface area of the IO carbon balls. The specific area of the mesopores-incorporated IO carbon balls was 1.3 times higher than that of bare IO carbon balls. Accordingly, the meso-/macroporous porous carbon balls exhibited higher electrocatalytic properties than the macroporous carbon balls.

  12. Microstructural characterization and thermodynamic analysis of precipitates in ultra-low-carbon bake hardened steel

    Energy Technology Data Exchange (ETDEWEB)

    Lee, Taeg-Woo [Department of Advanced Materials Science and Engineering, Kangwon National University, Chuncheon 200-701, Gangwon-do (Korea, Republic of); Kim, Sung-Il. [Sheet Products and Process Research Group, POSCO Technical Research Laboratories, 699, Gumho-dong, Gwangyang, Jeonnam 545-090 (Korea, Republic of); Hong, Moon-Hi [POSCO Center, 892 Daechi-4dong, Gangnam-gu, Seoul 135-777 (Korea, Republic of); Kim, Won-Yong [Gangwon Regional Division, Korea Institute of Industrial Technology, Gangneung 210-340 (Korea, Republic of); Yoo, Young-Gyu [Foundry Technology Center, Korea Institute of Industrial Technology, Incheon 404-170 (Korea, Republic of); Lim, Sung-Hwan, E-mail: shlim@kangwon.ac.kr [Department of Advanced Materials Science and Engineering, Kangwon National University, Chuncheon 200-701, Gangwon-do (Korea, Republic of)

    2014-01-05

    Highlights: • We provide the optimum amounts of Nb in ultra-low-carbon steel. • The density of fine precipitates and yield strength are closely connected. • The bake hardenability was mostly affected by a fine NbC precipitates. • The observed MnS–Cu{sub 2}S precipitate manifests a core–shell structure. -- Abstract: The effects of niobium (Nb) addition on the morphologies, size distributions, crystallography, and thermodynamics of precipitates in ultra-low-carbon bake hardened steels (ULC-BH) were investigated using energy-dispersive X-ray spectrometry (EDS), electron diffraction and high resolution transmission electron microscopy (TEM). The calculated nucleation rate of NbC precipitates indicate that the observed fine precipitates and saturation of yield strength with Nb 90 ppm steel are closely connected to thermodynamic factors. A TEM analysis was also carried out for other fine precipitates in two nitride modes: hexagonal AlN and fcc TiN. The Cu{sub 2}S–MnS complex precipitate was found to manifest a core–shell structure; the core part formed Cu{sub 2}S and the shell part formed MnS. MnS and Cu{sub 2}S have an orientation relationship between (001){sub MnS}//(001){sub Cu{sub 2S}} and [001]{sub MnS}//[001]{sub Cu{sub 2S}}.

  13. [Distribution of soil organic carbon in surface soil along a precipitation gradient in loess hilly area].

    Science.gov (United States)

    Sun, Long; Zhang, Guang-hui; Luan, Li-li; Li, Zhen-wei; Geng, Ren

    2016-02-01

    Along the 368-591 mm precipitation gradient, 7 survey sites, i.e. a total 63 investigated plots were selected. At each sites, woodland, grassland, and cropland with similar restoration age were selected to investigate soil organic carbon distribution in surface soil (0-30 cm), and the influence of factors, e.g. climate, soil depth, and land uses, on soil organic carbon distribution were analyzed. The result showed that, along the precipitation gradient, the grassland (8.70 g . kg-1) > woodland (7.88 g . kg-1) > farmland (7.73 g . kg-1) in concentration and the grassland (20.28 kg . m-2) > farmland (19.34 kg . m-2) > woodland (17.14 kg . m-2) in density. The differences of soil organic carbon concentration of three land uses were not significant. Further analysis of pooled data of three land uses showed that the surface soil organic carbon concentration differed significantly at different precipitation levels (Pcarbon concentration (r=0.838, Pcarbon increased with annual precipitation 0. 04 g . kg-1 . mm-1, density 0.08 kg . m-2 . mm-1. The soil organic carbon distribution was predicted with mean annual precipitation, soil clay content, plant litter in woodland, and root density in farmland.

  14. Preliminary assessment of a method utilizing carbon dioxide and steelmaking slags to produce precipitated calcium carbonate

    International Nuclear Information System (INIS)

    Highlights: ► An NH4-salt-based method utilizes CO2 and steelmaking slags to produce pure CaCO3. ► It was determined if its economic potential warrants moving forward. ► Despite small solvent losses, the method was found to have economical potential. ► The method has significant CO2 emissions reduction potential. ► Scaling up the reactor will allow for a more detailed design for the process. -- Abstract: One of the options that can contribute to the reduction of carbon dioxide emissions for climate change mitigation is the so-called CO2 sequestration by mineral carbonation, or CO2 mineral sequestration. Steel manufacturing could benefit from this option by utilizing its own by-products, i.e. steelmaking slags to combine with CO2. We have recently studied a method, where aqueous solution of ammonium salt (e.g. ammonium acetate, ammonium nitrate and ammonium chloride) is used to extract calcium selectively from the steel converter slag, followed by precipitation of pure calcium carbonate by bubbling CO2 through the produced solution. The ammonium salt solution is recovered and re-used. The purpose of this research was to determine if the economic potential of the method warrants moving forward to large-scale application. Despite the small solvent losses, the method was found to have economical potential. In addition, it has significant CO2 emission reduction potential as well. Scaling up the reactor from the small laboratory scale will allow more detailed design for the process to be made followed by a full economical evaluation including all of the important operational and capital investment costs.

  15. Liquid-Liquid Phase Separation in Supersaturated Lysozyme Solutions and Associated Precipitate Formation/Crystallization

    Science.gov (United States)

    Muschol, Martin; Rosenberger, Franz

    1997-01-01

    Using cloud point determinations, the phase boundaries (binodals) for metastable liquid-liquid (L-L) separation in supersaturated hen egg white lysozyme solutions with 3%, 5%, and 7% (wlv) NaCl at pH= 4.5 and protein concentrations c between 40 and 400 mg/ml were determined. The critical temperature for the binodal increased approximately linearly with salt concentration. The coexisting liquid phases both remained supersaturated but differed widely in protein concentration. No salt repartitioning was observed between the initial and the two separated liquid phases. After the L-L separation, due to the presence of the high protein concentration phase, crystallization occurred much more rapidly than in the initial solution. At high initial protein concentrations, a metastable gel phase formed at temperatures above the liquid binodal. Both crystal nucleation and gel formation were accelerated in samples that had been cycled through the binodal. Solutions in the gel and L-L regions yielded various types of precipitates. Based on theoretical considerations, previous observations with other proteins, and our experimental results with lysozyme, a generic phase diagram for globular proteins is put forth. A limited region in the (T,c) plane favorable for the growth of protein single crystals is delineated.

  16. Suppression of tin precipitation in SiSn alloy layers by implanted carbon

    Energy Technology Data Exchange (ETDEWEB)

    Gaiduk, P. I., E-mail: gaiduk@phys.au.dk [Department of Physics and Astronomy/iNANO, Aarhus University, Gustav Wieds Vej 14, DK-8000 Aarhus C (Denmark); Belarusian State University, prosp. Nezavisimosti 4, 220030 Minsk (Belarus); Lundsgaard Hansen, J., E-mail: johnlh@phys.au.dk; Nylandsted Larsen, A., E-mail: anl@phys.au.dk [Department of Physics and Astronomy/iNANO, Aarhus University, Gustav Wieds Vej 14, DK-8000 Aarhus C (Denmark); Bregolin, F. L., E-mail: f.lipp-bregolin@hzdr.de; Skorupa, W., E-mail: W.Skorupa@hzdr.de [Department of Semiconductor Materials, Helmholtz-Zentrum Dresden-Rossendorf, Bautzner Landstraße 400, 01328 Dresden (Germany)

    2014-06-09

    By combining transmission electron microscopy and Rutherford backscattering spectrometry, we have identified carbon related suppression of dislocations and tin precipitation in supersaturated molecular-beam epitaxial grown SiSn alloy layers. Secondary ion mass spectrometry has exposed the accumulation of carbon in the SiSn layers after high temperature carbon implantation and high temperature thermal treatment. Strain-enhanced separation of point defects and formation of dopant-defect complexes are suggested to be responsible for the effects. The possibility for carbon assisted segregation-free high temperature growth of heteroepitaxial SiSn/Si and GeSn/Si structures is argued.

  17. Exploring Carbon Nanomaterial Diversity for Nucleation of Protein Crystals

    Science.gov (United States)

    Govada, Lata; Leese, Hannah S.; Saridakis, Emmanuel; Kassen, Sean; Chain, Benny; Khurshid, Sahir; Menzel, Robert; Hu, Sheng; Shaffer, Milo S. P.; Chayen, Naomi E.

    2016-02-01

    Controlling crystal nucleation is a crucial step in obtaining high quality protein crystals for structure determination by X-ray crystallography. Carbon nanomaterials (CNMs) including carbon nanotubes, graphene oxide, and carbon black provide a range of surface topographies, porosities and length scales; functionalisation with two different approaches, gas phase radical grafting and liquid phase reductive grafting, provide routes to a range of oligomer functionalised products. These grafted materials, combined with a range of controls, were used in a large-scale assessment of the effectiveness for protein crystal nucleation of 20 different carbon nanomaterials on five proteins. This study has allowed a direct comparison of the key characteristics of carbon-based nucleants: appropriate surface chemistry, porosity and/or roughness are required. The most effective solid system tested in this study, carbon black nanoparticles functionalised with poly(ethylene glycol) methyl ether of mean molecular weight 5000, provides a novel highly effective nucleant, that was able to induce crystal nucleation of four out of the five proteins tested at metastable conditions.

  18. Can Mg isotopes be used to trace cyanobacteria-mediated magnesium carbonate precipitation in alkaline lakes?

    Directory of Open Access Journals (Sweden)

    L. S. Shirokova

    2011-07-01

    Full Text Available The fractionation of Mg isotopes was determined during the cyanobacterial mediated precipitation of hydrous magnesium carbonate precipitation in both natural environments and in the laboratory. Natural samples were obtained from Lake Salda (SE Turkey, one of the few modern environments on the Earth's surface where hydrous Mg-carbonates are the dominant precipitating minerals. This precipitation was associated with cyanobacterial stromatolites which were abundant in this aquatic ecosystem. Mg isotope analyses were performed on samples of incoming streams, groundwaters, lake waters, stromatolites, and hydromagnesite-rich sediments. Laboratory Mg carbonate precipitation experiments were conducted in the presence of purified Synechococcus sp cyanobacteria that were isolated from the lake water and stromatolites. The hydrous magnesium carbonates nesquehonite (MgCO3·3H2O and dypingite (Mg5(CO34(OH25(H2O were precipitated in these batch reactor experiments from aqueous solutions containing either synthetic NaHCO3/MgCl2 mixtures or natural Lake Salda water, in the presence and absence of live photosynthesizing Synechococcus sp. Bulk precipitation rates were not to affected by the presence of bacteria when air was bubbled through the system. In the stirred non-bubbled reactors, conditions similar to natural settings, bacterial photosynthesis provoked nesquehonite precipitation, whilst no precipitation occurred in bacteria-free systems in the absence of air bubbling, despite the fluids achieving a similar or higher degree of supersaturation. The extent of Mg isotope fractionation (Δ26Mgsolid-solution between the mineral and solution in the abiotic experiments was found to be identical, within uncertainty, to that measured in cyanobacteria-bearing experiments, and ranges from −1.4 to −0.7 ‰. This similarity refutes

  19. Interactions in the Geo-Biosphere: Processes of Carbonate Precipitation in Microbial Mats

    Science.gov (United States)

    Dupraz, C.; Visscher, P. T.

    2009-12-01

    Microbial communities are situated at the interface between the biosphere, the lithosphere and the hydrosphere. These microbes are key players in the global carbon cycle, where they influence the balance between the organic and inorganic carbon reservoirs. Microbial populations can be organized in microbial mats, which can be defined as organosedimentary biofilms that are dominated by cyanobacteria, and exhibit tight coupling of element cycles. Complex interactions between mat microbes and their surrounding environment can result in the precipitation of carbonate minerals. This process refers as ‘organomineralization sensu lato' (Dupraz et al. in press), which differs from ‘biomineralization’ (e.g., in shells and bones) by lacking genetic control on the mineral product. Organomineralization can be: (1) active, when microbial metabolic reactions are responsible for the precipitation (“biologically-induced” mineralization) or (2) passive, when mineralization within a microbial organic matrix is environmentally driven (e.g., through degassing or desiccation) (“biologically-influenced” mineralization). Studying microbe-mineral interactions is essential to many emerging fields of the biogeoscience, such as the study of life in extreme environments (e.g, deep biosphere), the origin of life, the search for traces of extraterrestrial life or the seek of new carbon sink. This research approach combines sedimentology, biogeochemistry and microbiology. Two tightly coupled components that control carbonate organomineralization s.l.: (1) the alkalinity engine and (2) the extracellular organic matter (EOM), which is ultimately the location of mineral nucleation. Carbonate alkalinity can be altered both by microbial metabolism and environmental factors. In microbial mats, the net accumulation of carbonate minerals often reflect the balance between metabolic activities that consume/produce CO2 and/or organic acids. For example, photosynthesis and sulfate reduction

  20. Sucrose/bovine serum albumin mediated biomimetic crystallization of calcium carbonate

    Indian Academy of Sciences (India)

    Cheng-Li Yao; Wang-Hua Xu; Ai-Min Ding; Jin-Mao Zhu

    2009-01-01

    To understand the role of the sucrose/bovine serum albumin system in the biomineralization process, we have tested the influence of different concentration of the sucrose/bovine serum albumin (BSA) on calcium carbonate (CaCO3) precipitation. The CaCO3 crystals were characterized by scanning electron microscope (SEM), Fourier transform infrared spectrograph (FT-IR) and powder X-ray diffractometry (XRD). The possible formation mechanism of CaCO3 in the sucrose/bovine serum albumin system was discussed.

  1. Crystal Chemistry of Carbonate Apatites from High-Pressure Synthesis

    Science.gov (United States)

    Fleet, M. E.; Liu, X.

    2007-12-01

    Relatively large (50-200 μm) crystals of carbonate-bearing hydroxylapatite (CHAP) and fluorapatite (CFAP) have been grown from carbonate-rich melts at 1-3 GPa and used to determine structural details beyond the resolution of Rietveld powder diffraction methods, using X-ray single-crystal structure and FTIR spectroscopy. The new information includes the structural location of the channel (type A) and phosphate group (type B) carbonate ions in various composition series, as well as the location of the excess fluoride anion in francolite, substitution mechanisms, and identification of the hydrogen carbonate (bicarbonate) ion as a new apatite channel species. For equivalent conditions of synthesis, the uptake of A-B carbonate is greater for Na-bearing CHAP (up to 2 carbonate ions pfu) than Na-bearing CFAP (about 0.4 pfu). The Na cation and A and B carbonate ions are locally coupled in ratios of 1:1:1 in CHAP and 1:1:2 in CFAP, to minimize the effects of charge compensation and spatial accommodation. An extensive data base of type A and B site occupancies reveals that the amount of A carbonate in type A-B CHAP and CFAP is considerably under represented by the relative band areas for asymmetric stretching (ν3) and out-of-plane bending (ν2) of carbonate in FTIR spectra. The weaker absorption intensity and shift to higher wavenumbers of type A bands indicates that the carbonate ion is bound more weakly in the apatite channel than in the interior of the crystal structure. Thus literature spectra for apatites, and especially for apatite biomineralisation, showing dominant amounts of B carbonate should be re-evaluated.

  2. Estimates of increased black carbon emissions from electrostatic precipitators during powdered activated carbon injection for mercury emissions control.

    Science.gov (United States)

    Clack, Herek L

    2012-07-01

    The behavior of mercury sorbents within electrostatic precipitators (ESPs) is not well-understood, despite a decade or more of full-scale testing. Recent laboratory results suggest that powdered activated carbon exhibits somewhat different collection behavior than fly ash in an ESP and particulate filters located at the outlet of ESPs have shown evidence of powdered activated carbon penetration during full-scale tests of sorbent injection for mercury emissions control. The present analysis considers a range of assumed differential ESP collection efficiencies for powdered activated carbon as compared to fly ash. Estimated emission rates of submicrometer powdered activated carbon are compared to estimated emission rates of particulate carbon on submicrometer fly ash, each corresponding to its respective collection efficiency. To the extent that any emitted powdered activated carbon exhibits size and optical characteristics similar to black carbon, such emissions could effectively constitute an increase in black carbon emissions from coal-based stationary power generation. The results reveal that even for the low injection rates associated with chemically impregnated carbons, submicrometer particulate carbon emissions can easily double if the submicrometer fraction of the native fly ash has a low carbon content. Increasing sorbent injection rates, larger collection efficiency differentials as compared to fly ash, and decreasing sorbent particle size all lead to increases in the estimated submicrometer particulate carbon emissions.

  3. Precipitation diagram and optimization of crystallization conditions at low ionic strength for deglycosylated dye-decolorizing peroxidase from a basidiomycete

    International Nuclear Information System (INIS)

    Precipitation phase diagrams can be rapidly constructed using dispensing-robot technology. These diagrams provide information that assists in optimization of crystal growth. The growth of suitably sized protein crystals is essential for protein structure determination by X-ray crystallography. In general, crystals are grown using a trial-and-error method. However, these methods have been modified with the advent of microlitre dispensing-robot technology and of protocols that rapidly screen for crystal nucleation conditions. The use of one such automatic dispenser for mixing protein drops (1.3–2.0 µl in volume) of known concentration and pH with precipitating solutions (ejecting 2.0 µl droplets) containing salt is described here. The results of the experiments are relevant to a crystallization approach based on a two-step procedure: screening for the crystal nucleation step employing robotics followed by optimization of the crystallization conditions using incomplete factorial experimental design. Large crystals have successfully been obtained using quantities as small as 3.52 mg protein

  4. Morphological changes of gamma prime precipitates in nickel-base superalloy single crystals

    International Nuclear Information System (INIS)

    Changes in the morphology of the gamma prime precipitate were examined during tensile creep at temperatures between 927 and 1038 C in 001-oriented single crystals of a Ni-Al-Mo-Ta superalloy. In this alloy, which has a large negative misfit of -0.80%, the gamma prime particles link together during creep to form platelets, or rafts, which are aligned with their broad faces perpendicular to the applied tensile axis. The dimensions of the gamma and gamma prime phases were measured as directional coarsening developed in an attempt to trace the changing morphology under various stress levels. In addition, the effects of initial microstructure, as well as slight compositional variations, were related to raft development and creep properties. The results showed that directional coarsening of gamma prime began during primary creep, and under certain conditions, continued to develop after the onset of steady-state creep. The length of the rafts increased linearly with time up to a plateau region. The thickness of the rafts, however, remained equal to the initial gamma prime size at least up through the onset of tertiary creep this is a clear indication of the stability of the finely-spaced gamma-gamma prime lamellar structure. It was found that the single crystals with the finest gamma prime size exhibited the longest creep lives, because the resultant rafted structure had a larger number of gamma-gamma prime interfaces per unit volume of material

  5. Enhancing the Effectiveness of Carbon Dioxide Flooding by Managing Asphaltene Precipitation

    Energy Technology Data Exchange (ETDEWEB)

    Deo, Milind D.

    2002-02-21

    This project was undertaken to understand fundamental aspects of carbon dioxide (CO2) induced asphaltene precipitation. Oil and asphaltene samples from the Rangely field in Colorado were used for most of the project. The project consisted of pure component and high-pressure, thermodynamic experiments, thermodynamic modeling, kinetic experiments and modeling, targeted corefloods and compositional modeling.

  6. A wet electrostatic precipitator (WESP) as countermeasure to mist formation in amine based carbon capture

    NARCIS (Netherlands)

    Mertens, J.; Anderlohr, C.; Rogiers, P.; Brachert, L.; Khakharia, P.M.; Goetheer, E.L.V.; Schaber, K.

    2014-01-01

    This study is to our knowledge the first to evaluate the potential of a wet electrostatic precipitator (WESP) to prevent aerosol formation issues inside amine based carbon capture installations. A WESP is a suitable option since this study proves that it is very efficient for the removal of the mist

  7. Carbon-13 NMR studies of liquid crystals

    International Nuclear Information System (INIS)

    High resolution, proton decoupled 13C nmr are observed for a series of neat nematic liquid crystals, the p-alkoxyazoxybenzenes, and a smectic-A liquid crystal, diethylazoxydibenzoate in a magnetic field of 23 kG. The (uniaxial) order parameters S = less than P2(costheta) greater than are found to be about 0.4 and 0.9 for the nematic and smectic-A phase respectively at the clearing points. The order parameter increases with decreasing temperature in the nematic phase but is constant, or nearly so, with temperature in the smectic-A phase. In the nematic series studied, the ordering exhibits an even-odd alternation along the series and qualitative agreement with a recent theory due to Marcelja is found. In both phases, the spectra show that the molecule rotates rapidly about its long axis. Tentative conclusions about molecular conformational motion and 14N spin relaxation are presented for both nematic and smectic-A phases. In the smectic-A phase, the sample is rotated about an axis perpendicular to H0 and the resulting spectra are dicusssed. The theory of observed chemical shifts in liquid crystals is discussed and equations are derived which relate the nmr spectra of liquid-crystals to the order parameters. A model for the smectic-C phase due to Luz and Meiboom and Doane is described and lineshapes are determined on the basis of this model for special cases. The dependence of the order parameters on the molecular potential which give rise to the various degrees of order in the different liquid crystalline phases is examined. To a good approximation the functional dependence of the order parameters on the molecular potential is shown to be a simple one in the limit of small tilt angle in the smectic-C phase

  8. Precipitation kinetics of Mg-carbonates, influence of organic ligands and consequences for CO2 mineral sequestration

    International Nuclear Information System (INIS)

    Forming magnesium carbonate minerals through carbonation of magnesium silicates has been proposed as a safe and durable way to store carbon dioxide, with a possibly high potential to offset anthropogenic CO2 emissions. To date however, chemical reactions involved in this process are facing strong kinetic limitations, which originate in the low reactivity of both Mg-silicates and Mg-carbonates. Numerous studies have focused on the dissolution of Mg-silicates, under the questionable hypothesis that this step limits the whole process. This thesis work focuses instead on the mechanisms and rates of formation of magnesium carbonates, which are the final products of carbonation reactions. The first part of the work is dedicated to studying the influence on magnesite precipitation kinetics of three organic ligands known to accelerate Mg-silicates dissolution rates: oxalate, citrate and EDTA. With help of mixed-flow reactor experiments performed between 100 and 150 C, we show that these ligands significantly reduce magnesite growth rates, through two combined mechanisms: (1) complexation of Mg2+ cations in aqueous solution, which was rigorously estimated from a thermodynamic database established through a critical review of the literature, and (2) adsorption of ligands to a limited number of surface sites, leading to a decrease of the precipitation rate constant. The observed growth inhibition is maximal with citrate. We then used hydrothermal atomic force microscopy to probe the origin of the documented growth inhibition. Our observations show that citrate and oxalate interact with the crystal growth process on magnesite surface, modifying the shape of growth hillocks as well as the step generation frequency through spiral growth. We also show that the ligands adsorb preferentially on different kink-sites, which is probably related to their different structures and chemical properties. We propose that the stronger magnesite growth inhibition caused by citrate is related

  9. Thermal properties of single-walled carbon nanotube crystal

    Institute of Scientific and Technical Information of China (English)

    Hu Li-Jun; Liu Ji; Liu Zheng; Qiu Cai-Yu; Zhou Hai-Qing; Sun Lian-Feng

    2011-01-01

    In this work,the thermal properties of a single-walled carbon nanotube (SWCNT) crystal are studied. The thermal conductivity of the SWCNT crystal is found to have a linear dependence on temperature in the temperature range from 1.9 K to 100.0 K. In addition,a peak (658 W/mK) is found at a temperature of about 100.0 K. The thermal conductivity decreases gradually to a value of 480 W/mK and keeps almost a constant in the temperature range from 100.0 K to 300.0 K. Meanwhile,the specific heat shows an obvious linear relationship with temperature in the temperature range from 1.9 K to 300.0 K. We discuss the possible mechanisms for these unique thermal properties of the single-walled carbon nanotube crystal.

  10. The sensitivity of carbon exchanges in Great Plains grasslands to precipitation variability

    Science.gov (United States)

    Petrie, M. D.; Brunsell, N. A.; Vargas, R.; Collins, S. L.; Flanagan, L. B.; Hanan, N. P.; Litvak, M. E.; Suyker, A. E.

    2016-02-01

    In the Great Plains, grassland carbon dynamics differ across broad gradients of precipitation and temperature, yet finer-scale variation in these variables may also affect grassland processes. Despite the importance of grasslands, there is little information on how fine-scale relationships compare between them regionally. We compared grassland C exchanges, energy partitioning and precipitation variability in eight sites in the eastern and western Great Plains using eddy covariance and meteorological data. During our study, both eastern and western grasslands varied between an average net carbon sink and a net source. Eastern grasslands had a moderate vapor pressure deficit (VPD = 0.95 kPa) and high growing season gross primary productivity (GPP = 1010 ± 218 g C m-2 yr-1). Western grasslands had a growing season with higher VPD (1.43 kPa) and lower GPP (360 ± 127 g C m-2 yr-1). Western grasslands were sensitive to precipitation at daily timescales, whereas eastern grasslands were sensitive at monthly and seasonal timescales. Our results support the expectation that C exchanges in these grasslands differ as a result of varying precipitation regimes. Because eastern grasslands are less influenced by short-term variability in rainfall than western grasslands, the effects of precipitation change are likely to be more predictable in eastern grasslands because the timescales of variability that must be resolved are relatively longer. We postulate increasing regional heterogeneity in grassland C exchanges in the Great Plains in coming decades.

  11. Combined hydrogen production and storage with subsequent carbon crystallization.

    Science.gov (United States)

    Lueking, Angela D; Gutierrez, Humberto R; Fonseca, Dania A; Narayanan, Deepa L; Van Essendelft, Dirk; Jain, Puja; Clifford, Caroline E B

    2006-06-21

    We provide evidence of low-temperature hydrogen evolution and possible hydrogen trapping in an anthracite coal derivative, formed via reactive ball milling with cyclohexene. No molecular hydrogen is added to the process. Raman-active molecular hydrogen vibrations are apparent in samples at atmospheric conditions (300 K, 1 bar) for samples prepared 1 year previously and stored in ambient air. Hydrogen evolves slowly at room temperature and is accelerated upon sample heating, with a first increase in hydrogen evolution occurring at approximately 60 degrees C. Subsequent chemical modification leads to the observation of crystalline carbons, including nanocrystalline diamond surrounded by graphene ribbons, other sp2-sp3 transition regions, purely graphitic regions, and a previously unidentified crystalline carbon form surrounded by amorphous carbon. The combined evidence for hydrogen trapping and carbon crystallization suggests hydrogen-induced crystallization of the amorphous carbon materials, as metastable hydrogenated carbons formed via the high-energy milling process rearrange into more thermodynamically stable carbon forms and molecular hydrogen.

  12. Influence of management and precipitation on carbon fluxes in greatplains grasslands

    Science.gov (United States)

    Rigge, Matthew B.; Wylie, Bruce K.; Zhang, Li; Boyte, Stephen P.

    2013-01-01

    Suitable management and sufficient precipitation on grasslands can provide carbon sinks. The net carbon accumulation of a site from the atmosphere, modeled as the Net Ecosystem Productivity (NEP), is a useful means to gauge carbon balance. Previous research has developed methods to integrate flux tower data with satellite biophysical datasets to estimate NEP across large regions. A related method uses the Ecosystem Performance Anomaly (EPA) as a satellite-derived indicator of disturbance intensity (e.g., livestock stocking rate, fire, and insect damage). To better understand the interactions among management, climate, and carbon dynamics, we evaluated the relationship between EPA and NEP data at the 250 m scale for grasslands in the Central Great Plains, USA (ranging from semi-arid to mesic). We also used weekly estimates of NEP to evaluate the phenology of carbon dynamics, classified by EPA (i.e., by level of disturbance impact). Results show that the cumulative carbon balance over these grasslands from 2000 to 2008 was a weak net sink of 13.7 g C m−2 yr−1. Overall, NEP increased with precipitation (R2 = 0.39, P management practices in the tallgrass and mixed-grass prairie may potentially induce a period of average net carbon sink until a new equilibrium soil organic carbon is achieved. In the shortgrass prairie, management should be considered sustainable if carbon stocks are simply maintained. The consideration of site carbon balance adds to the already difficult task of managing grasslands appropriately to site conditions. Results clarify the seasonal and interannual dynamics of NEP, specifically the influence of disturbance and moisture availability.

  13. Geophysical monitoring and reactive transport modeling of ureolytically-driven calcium carbonate precipitation

    Energy Technology Data Exchange (ETDEWEB)

    Wu, Y.; Ajo-Franklin, J.B.; Spycher, N.; Hubbard, S.S.; Zhang, G.; Williams, K.H.; Taylor, J.; Fujita, Y.; Smith, R.

    2011-07-15

    Ureolytically-driven calcium carbonate precipitation is the basis for a promising in-situ remediation method for sequestration of divalent radionuclide and trace metal ions. It has also been proposed for use in geotechnical engineering for soil strengthening applications. Monitoring the occurrence, spatial distribution, and temporal evolution of calcium carbonate precipitation in the subsurface is critical for evaluating the performance of this technology and for developing the predictive models needed for engineering application. In this study, we conducted laboratory column experiments using natural sediment and groundwater to evaluate the utility of geophysical (complex resistivity and seismic) sensing methods, dynamic synchrotron x-ray computed tomography (micro-CT), and reactive transport modeling for tracking ureolytically-driven calcium carbonate precipitation processes under site relevant conditions. Reactive transport modeling with TOUGHREACT successfully simulated the changes of the major chemical components during urea hydrolysis. Even at the relatively low level of urea hydrolysis observed in the experiments, the simulations predicted an enhanced calcium carbonate precipitation rate that was 3-4 times greater than the baseline level. Reactive transport modeling results, geophysical monitoring data and micro-CT imaging correlated well with reaction processes validated by geochemical data. In particular, increases in ionic strength of the pore fluid during urea hydrolysis predicted by geochemical modeling were successfully captured by electrical conductivity measurements and confirmed by geochemical data. The low level of urea hydrolysis and calcium carbonate precipitation suggested by the model and geochemical data was corroborated by minor changes in seismic P-wave velocity measurements and micro-CT imaging; the latter provided direct evidence of sparsely distributed calcium carbonate precipitation. Ion exchange processes promoted through NH{sub 4}{sup

  14. Geophysical monitoring and reactive transport modeling of ureolytically-driven calcium carbonate precipitation

    Directory of Open Access Journals (Sweden)

    Taylor Joanna

    2011-09-01

    Full Text Available Abstract Ureolytically-driven calcium carbonate precipitation is the basis for a promising in-situ remediation method for sequestration of divalent radionuclide and trace metal ions. It has also been proposed for use in geotechnical engineering for soil strengthening applications. Monitoring the occurrence, spatial distribution, and temporal evolution of calcium carbonate precipitation in the subsurface is critical for evaluating the performance of this technology and for developing the predictive models needed for engineering application. In this study, we conducted laboratory column experiments using natural sediment and groundwater to evaluate the utility of geophysical (complex resistivity and seismic sensing methods, dynamic synchrotron x-ray computed tomography (micro-CT, and reactive transport modeling for tracking ureolytically-driven calcium carbonate precipitation processes under site relevant conditions. Reactive transport modeling with TOUGHREACT successfully simulated the changes of the major chemical components during urea hydrolysis. Even at the relatively low level of urea hydrolysis observed in the experiments, the simulations predicted an enhanced calcium carbonate precipitation rate that was 3-4 times greater than the baseline level. Reactive transport modeling results, geophysical monitoring data and micro-CT imaging correlated well with reaction processes validated by geochemical data. In particular, increases in ionic strength of the pore fluid during urea hydrolysis predicted by geochemical modeling were successfully captured by electrical conductivity measurements and confirmed by geochemical data. The low level of urea hydrolysis and calcium carbonate precipitation suggested by the model and geochemical data was corroborated by minor changes in seismic P-wave velocity measurements and micro-CT imaging; the latter provided direct evidence of sparsely distributed calcium carbonate precipitation. Ion exchange processes

  15. Bioprecipitation of Calcium Carbonate Crystals by Bacteria Isolated from Saline Environments Grown in Culture Media Amended with Seawater and Real Brine

    Science.gov (United States)

    Silva-Castro, G. A.; Uad, I.; Gonzalez-Martinez, A.; Rivadeneyra, A.; Gonzalez-Lopez, J.; Rivadeneyra, M. A.

    2015-01-01

    The precipitation of calcium carbonate and calcium sulphate by isolated bacteria from seawater and real brine obtained in a desalination plant growth in culture media containing seawater and brine as mineral sources has been studied. However, only bioprecipitation was detected when the bacteria were grown in media with added organic matter. Biomineralization process started rapidly, crystal formation taking place in the beginning a few days after inoculation of media; roughly 90% of total cultivated bacteria showed. Six major colonies with carbonate precipitation capacity dominated bacterial community structure cultivated in heterotrophic platable bacteria medium. Taxonomic identification of these six strains through partial 16S rRNA gene sequences showed their affiliation with Gram-positive Bacillus and Virgibacillus genera. These strains were able to form calcium carbonate minerals, which precipitated as calcite and aragonite crystals and showed bacterial fingerprints or bacteria calcification. Also, carbonic anhydrase activity was observed in three of these isolated bacteria. The results of this research suggest that microbiota isolated from sea water and brine is capable of precipitation of carbonate biominerals, which can occur in situ with mediation of organic matter concentrations. Moreover, calcium carbonate precipitation ability of this microbiota could be of importance in bioremediation of CO2 and calcium in certain environments. PMID:26273646

  16. Bioprecipitation of Calcium Carbonate Crystals by Bacteria Isolated from Saline Environments Grown in Culture Media Amended with Seawater and Real Brine

    Directory of Open Access Journals (Sweden)

    G. A. Silva-Castro

    2015-01-01

    Full Text Available The precipitation of calcium carbonate and calcium sulphate by isolated bacteria from seawater and real brine obtained in a desalination plant growth in culture media containing seawater and brine as mineral sources has been studied. However, only bioprecipitation was detected when the bacteria were grown in media with added organic matter. Biomineralization process started rapidly, crystal formation taking place in the beginning a few days after inoculation of media; roughly 90% of total cultivated bacteria showed. Six major colonies with carbonate precipitation capacity dominated bacterial community structure cultivated in heterotrophic platable bacteria medium. Taxonomic identification of these six strains through partial 16S rRNA gene sequences showed their affiliation with Gram-positive Bacillus and Virgibacillus genera. These strains were able to form calcium carbonate minerals, which precipitated as calcite and aragonite crystals and showed bacterial fingerprints or bacteria calcification. Also, carbonic anhydrase activity was observed in three of these isolated bacteria. The results of this research suggest that microbiota isolated from sea water and brine is capable of precipitation of carbonate biominerals, which can occur in situ with mediation of organic matter concentrations. Moreover, calcium carbonate precipitation ability of this microbiota could be of importance in bioremediation of CO2 and calcium in certain environments.

  17. Bioprecipitation of Calcium Carbonate Crystals by Bacteria Isolated from Saline Environments Grown in Culture Media Amended with Seawater and Real Brine.

    Science.gov (United States)

    Silva-Castro, G A; Uad, I; Gonzalez-Martinez, A; Rivadeneyra, A; Gonzalez-Lopez, J; Rivadeneyra, M A

    2015-01-01

    The precipitation of calcium carbonate and calcium sulphate by isolated bacteria from seawater and real brine obtained in a desalination plant growth in culture media containing seawater and brine as mineral sources has been studied. However, only bioprecipitation was detected when the bacteria were grown in media with added organic matter. Biomineralization process started rapidly, crystal formation taking place in the beginning a few days after inoculation of media; roughly 90% of total cultivated bacteria showed. Six major colonies with carbonate precipitation capacity dominated bacterial community structure cultivated in heterotrophic platable bacteria medium. Taxonomic identification of these six strains through partial 16S rRNA gene sequences showed their affiliation with Gram-positive Bacillus and Virgibacillus genera. These strains were able to form calcium carbonate minerals, which precipitated as calcite and aragonite crystals and showed bacterial fingerprints or bacteria calcification. Also, carbonic anhydrase activity was observed in three of these isolated bacteria. The results of this research suggest that microbiota isolated from sea water and brine is capable of precipitation of carbonate biominerals, which can occur in situ with mediation of organic matter concentrations. Moreover, calcium carbonate precipitation ability of this microbiota could be of importance in bioremediation of CO2 and calcium in certain environments. PMID:26273646

  18. Bioactive coatings on Portland cement substrates: Surface precipitation of apatite-like crystals

    Energy Technology Data Exchange (ETDEWEB)

    Gallego, Daniel [Biomedical Engineering Department, Ohio State University, 1080 Carmack Road, 270 Bevis Hall, Columbus (OH) - 43210 (United States); Higuita, Natalia [Biomedical Engineering Department, Ohio State University, 1080 Carmack Road, 270 Bevis Hall, Columbus (OH) - 43210 (United States); Grupo de Investigacion en Ingenieria Biomedica CES-EIA (GIBEC), Carrera 43 A No. 52 Sur - 99, Sabaneta (Colombia); Garcia, Felipe [Grupo de Investigacion en Ingenieria Biomedica CES-EIA (GIBEC), Carrera 43 A No. 52 Sur - 99, Sabaneta (Colombia); Ferrell, Nicholas [Biomedical Engineering Department, Ohio State University, 1080 Carmack Road, 270 Bevis Hall, Columbus (OH) - 43210 (United States); Hansford, Derek J. [Biomedical Engineering Department, Ohio State University, 1080 Carmack Road, 270 Bevis Hall, Columbus (OH) - 43210 (United States)], E-mail: hansford.4@osu.edu

    2008-04-01

    We report a method for depositing bioactive coatings onto cement materials for bone tissue engineering applications. White Portland cement substrates were hydrated under a 20% CO{sub 2} atmosphere, allowing the formation of CaCO{sub 3}. The substrates were incubated in a calcium phosphate solution for 1, 3, and 6 days (CPI, CPII, and CPIII respectively) at 37 deg. C to induce the formation of carbonated apatite. Cement controls were prepared and hydrated with and without CO{sub 2} atmosphere (C+ and C- respectively). The presence of apatite-like crystals was verified by Scanning Electron Microscopy (SEM) and Energy Dispersive Spectroscopy (EDS). The substrate cytocompatibility was evaluated via SEM after 24 hour cell cultures. SEM revealed the presence Ca(OH){sub 2} on C-, and CaCO{sub 3} on C+. Apatite-like crystals were detected only on CPIII, confirmed by phosphorus EDS peaks only for CPIII. Cells attached and proliferated similarly well on all the substrates except C-. These results prove the feasibility of obtaining biocompatible and bioactive coatings on Portland cement for bone tissue engineering applications.

  19. Separation of 1,3-propanediol from glycerol-based fermentations of Klebsiella pneumoniae by alcohol precipitation and dilution crystallization

    Institute of Scientific and Technical Information of China (English)

    GAO Sujun; ZHANG Daijia; SUN Yaqin; XIU Zhilong

    2007-01-01

    The separation of 1,3-propanediol from the glycerol-based fermentation broth of Klebsiella pneumoniae plays an important role during the microbial production of 1,3-propanediol.In this paper,the separation of 1,3-propanediol from fermentative broth by a combination of ultrafiltration and alcohol dilution crystallization was investigated.The broth was first filtered by ultrafiltration,and 99%of cells,89.4% of proteins and 69% of nucleic acids were removed.The obtained broth was further condensed by vacuum distillation,and then alcohol was added.The macromolecular impurities,such as nucleic acids,polysaccharides and proteins,were precipitated,and inorganic and organic salts were crystallized.The optimal volume ratio of alcohol added to the condensed fermentation broth was determined to tivity decreased by 97.4%,89.7% and 95.8%,respectively,compared with the fermentative broth.The influences of pH and water content in condensed broth on alcohol precipitation and dilution crystallization were also investigated.The experimental results indicated that alcohol precipitation and dilution crystallization was feasible and effective for the separation of 1,3-propanediol from actual fermentation broth.

  20. The influence of electron discharge and magnetic field on calcium carbonate (CaCO3) precipitation

    Science.gov (United States)

    Putro, Triswantoro; Endarko

    2016-04-01

    The influences of electron discharge and magnetic field on calcium carbonate (CaCO3) precipitation in water have been successfully investigated. The study used three pairs of magnetic field 0.1 T whilst the electron discharge was generated from television flyback transformer type BW00607 and stainless steel SUS 304 as an electrode. The water sample with an initial condition of 230 mg/L placed in the reactor with flow rate 375 mL/minutes, result showed that the electron discharge can be reduced contain of calcium carbonate the water sample around 17.39% within 2 hours. Meanwhile for the same long period of treatment and flow rate, around 56.69% from initial condition of 520 mg/L of calcium carbonate in the water sample can be achieved by three pairs of magnetic field 0.1 T. When the combination of three pairs of magnetic field 0.1 T and the electron discharge used for treatment, the result showed that the combination of electron discharge and magnetic field methods can be used to precipitate calcium carbonate in the water sample 300 mg/L around 76.66% for 2 hours of treatment. The study then investigated the influence of the polar position of the magnetic field on calcium carbonate precipitation. Two positions of magnetic field were tested namely the system with alternated polar magnetics and the system without inversion of the polar magnetics. The influence of the polar position showed that the percentage reduction in levels of calcium carbonate in the water sample (360 mg/L) is significant different. Result showed that the system without inversion of the polar magnetics is generally lower than the system with alternated polar magnetics, with reduction level at 30.55 and 57.69%, respectively.

  1. Effect of a cyanobacterial community on calcium carbonate precipitation in Puente del Inca (Mendoza, Argentina)

    OpenAIRE

    Ferrari, S.G.; Italiano, M.C.; de Silva, H J

    2002-01-01

    The involvement of cyanobacteria in the precipitation process forming calcium carbonate was studied in samples collected at a geothermal spring located in an area close to Puente del Inca (Mendoza, Argentina). In the summer season profuse cyanobacterial growth is observed at Puente del Inca in areas exposed to sunlight and over which thermal water flows. Differences in cellular structure allowed the recognition of strains of Oscillatoria, Spirulina, Plectonema, and Nostoc, Oscillatoria and...

  2. Nano-sized precipitation and properties of a low carbon niobium micro-alloyed bainitic steel

    International Nuclear Information System (INIS)

    The present work focuses on microstructure evolution and precipitation strengthening during tempering at region of 550–680 °C to elucidate the structure–property relationship in the steel. The effect of tempering on the development of a 700 MPa grade high strength hot rolled cost-effective bainitic steel was studied for infrastructure applications. Granular bainite with dispersed martenisit–austenite (M–A) constituents in the bainitic ferrite matrix was obtained after hot rolling and air cooling to room temperature. The decomposition of M–A constituents to cementite carbides and the precipitation of nano-sized NbC carbides in bainitic matrix on tempering were characterized by scanning electron microscopy (SEM) and transmission electron microscopy (TEM). Nano-sized precipitates of NbC precipitated during tempering were in average diameter of ~4.1–6.1 nm. There were ~86–173 MPa increases in yield strength after tempering at region of 550–680 °C. It is noticeable that those nano-sized NbC precipitates provide an effective way to significantly increase the strength of the low carbon bainitic steel. High yield strength of 716 MPa with high ductility (uniform elongation of 9.3% and total elongation of 22.4%), low yield to tensile ratio of 0.9 and good low temperature toughness of 47 J (half thickness) at –40 °C was obtained after tempering at 680 °C for 30 min

  3. Investigation of Black Carbon Effects on Precipitation and Surface Hydrology over the Western United States

    Science.gov (United States)

    Tseng, H. L. R.; Liou, K. N.; Gu, Y.; Fovell, R. G.; Li, Q.

    2015-12-01

    The current Exceptional Drought (US Drought Monitor) over the western United States warrants an in-depth investigation of possible causes of decreased precipitation and surface hydrology. Black carbon (BC), being the most radiatively-absorptive of any aerosol species, has the potential to semi-directly influence atmospheric physics and dynamics. Aloft, BC can exacerbate the aridity in some areas while increasing precipitation in other locations. On the surface, BC can also alter surface hydrology parameters such as surface runoff and snow water equivalent. In this study, we examine the role of BC and its possible effect on spatial precipitation redistribution and surface hydrology west of and over the Rocky Mountains from an online and coupled meteorological and chemical perspective. In particular, we utilize the Weather Research and Forecasting-Chemistry (WRF-Chem) model at the horizontal resolution of 30 km, employing the Fu-Liou-Gu plane-parallel radiation scheme and a three-dimensional radiation parameterization over mountainous areas to account for BC feedback with clouds, radiation, local circulation, and precipitation. Preliminary results of a January 2005 low pressure system show the inclusion of BC increases (decreases) precipitation on the windward (leeward) side of the Transverse and Peninsular Ranges, and the Sierra Nevada. Results also show BC contributes to an increase in surface runoff on the windward side of the Transverse and Peninsular Ranges, the Sierra Nevada, and Rocky Mountains, but a decrease in snow water equivalent over Sierra Nevada and Rocky Mountains.

  4. Nano-sized precipitation and properties of a low carbon niobium micro-alloyed bainitic steel

    Energy Technology Data Exchange (ETDEWEB)

    Xie, Z.J. [School of Materials Science and Engineering, University of Science and Technology Beijing, Beijing 100083 (China); Department of Materials Science and Engineering, McMaster University, Hamilton L8S 4L8 (Canada); Ma, X.P. [Department of Materials Science and Engineering, McMaster University, Hamilton L8S 4L8 (Canada); Shang, C.J., E-mail: cjshang@ustb.edu.cn [School of Materials Science and Engineering, University of Science and Technology Beijing, Beijing 100083 (China); Wang, X.M. [School of Materials Science and Engineering, University of Science and Technology Beijing, Beijing 100083 (China); Subramanian, S.V. [Department of Materials Science and Engineering, McMaster University, Hamilton L8S 4L8 (Canada)

    2015-08-12

    The present work focuses on microstructure evolution and precipitation strengthening during tempering at region of 550–680 °C to elucidate the structure–property relationship in the steel. The effect of tempering on the development of a 700 MPa grade high strength hot rolled cost-effective bainitic steel was studied for infrastructure applications. Granular bainite with dispersed martenisit–austenite (M–A) constituents in the bainitic ferrite matrix was obtained after hot rolling and air cooling to room temperature. The decomposition of M–A constituents to cementite carbides and the precipitation of nano-sized NbC carbides in bainitic matrix on tempering were characterized by scanning electron microscopy (SEM) and transmission electron microscopy (TEM). Nano-sized precipitates of NbC precipitated during tempering were in average diameter of ~4.1–6.1 nm. There were ~86–173 MPa increases in yield strength after tempering at region of 550–680 °C. It is noticeable that those nano-sized NbC precipitates provide an effective way to significantly increase the strength of the low carbon bainitic steel. High yield strength of 716 MPa with high ductility (uniform elongation of 9.3% and total elongation of 22.4%), low yield to tensile ratio of 0.9 and good low temperature toughness of 47 J (half thickness) at –40 °C was obtained after tempering at 680 °C for 30 min.

  5. Magnesium isotope fractionation during hydrous magnesium carbonate precipitation with and without cyanobacteria

    Science.gov (United States)

    Mavromatis, Vasileios; Pearce, Christopher R.; Shirokova, Liudmila S.; Bundeleva, Irina A.; Pokrovsky, Oleg S.; Benezeth, Pascale; Oelkers, Eric H.

    2012-01-01

    The hydrous magnesium carbonates, nesquehonite (MgCO 3·3H 2O) and dypingite (Mg 5(CO 3) 4(OH) 2·5(H 2O)), were precipitated at 25 °C in batch reactors from aqueous solutions containing 0.05 M NaHCO 3 and 0.025 M MgCl 2 and in the presence and absence of live photosynthesizing Gloeocapsa sp. cyanobacteria. Experiments were performed under a variety of conditions; the reactive fluid/bacteria/mineral suspensions were continuously stirred, and/or air bubbled in most experiments, and exposed to various durations of light exposure. Bulk precipitation rates are not affected by the presence of bacteria although the solution pH and the degree of fluid supersaturation with respect to magnesium carbonates increase due to photosynthesis. Lighter Mg isotopes are preferentially incorporated into the precipitated solids in all experiments. Mg isotope fractionation between the mineral and fluid in the abiotic experiments is identical, within uncertainty, to that measured in cyanobacteria-bearing experiments; measured δ 26Mg ranges from -1.54‰ to -1.16‰ in all experiments. Mg isotope fractionation is also found to be independent of reactive solution pH and Mg, CO 32-, and biomass concentrations. Taken together, these observations suggest that Gloeocapsa sp. cyanobacterium does not appreciably affect magnesium isotope fractionation between aqueous fluid and hydrous magnesium carbonates.

  6. Heterocystous Cyanobacteria in Microbialites Play an Important Role in N2 Fixation and Carbonate Mineral Precipitation

    Science.gov (United States)

    Alcantara-Hernandez, R. J.

    2015-12-01

    Lake Alchichica is a maars type crater-lake located in Central Mexico (pH > 8.9, EC ~13.39 mS cm-1). This limnological system harbors two types of microbialites that can be found around the entire perimeter of the lake (Fig. 1). These structures are representative examples of complex and diverse microbiological assemblages, where microbial activity promotes lithification by trapping, binding and/or precipitating detrital or chemical sediments. Previous studies determined that the microbialites of Lake Alchichica fix N2 to thrive under the N-limiting conditions of the lake, and that these nitrogenase activity peaks are related to heterocystous cyanobacteria that couple photosynthesis to N2 fixation during daylight periods. Heterocystous cyanobacteria (Nostocales) together with Oscillatoriales (non-heterocystous filamentous cyanobacteria) and other cyanobacterial groups have been described as the most abundant cyanobacteria in Alchichica microbialites, and in lithifying mats. Our results suggest that heterocystous cyanobacteria play an important role not only by fixing N2 for biomass construction, but also because their heterocysts host in their external cell membranes main sites for carbonate mineral precipitation including calcium carbonates and siderite. Previous research has shown that the heterocyst is the specialized site for cellular respiration associated to the pH decrease of vegetative/photosynthetic cells, contributing thus to the precipitation of carbonates and the accretion of the organosedimentary structure

  7. Exploring biotic vs. abiotic controls on syngenetic carbonate and clay mineral precipitation

    Science.gov (United States)

    Nascimento, Gabriela S.; McKenzie, Judith A.; Martinez Ruiz, Francisca; Bontognali, Tomaso R. R.; Vasconcelos, Crisogono

    2016-04-01

    A possible syngenetic relationship between carbonate and clay mineral precipitation has been reported for sedimentary rocks deposited in both lacustrine and marine sedimentary environments throughout the geological record. In particular, the mineral dolomite is often found associated with Mg-rich clays, such as stevensite. It is notable that this carbonate/clay association has been recorded in numerous samples taken from modern dolomite precipitating environments; for example, the Coorong lakes, South Australia, coastal sabkhas, Abu Dhabi, UAE and coastal hypersaline lagoons (Lagoa Vermelha and Brejo do Espinho) east of Rio de Janeiro, Brazil. An HRTEM study of samples from these three locations indicates a possible physical/chemical association between the Ca-dolomite and Mg-rich clays, demonstrating a probable co-precipitation. To test this hypothesis, we have conducted a series of biotic and abiotic laboratory experiments. If this syngenesis actually occurs in nature, what, if any, are the biogeochemical processes controlling these precipitation reactions? Our experiments were designed to determine the extent of the biotic versus abiotic component influencing the mineral precipitation and, in the case of a biotic influence, to understand the mechanism through which microorganisms might mediate the formation of clay minerals. The experiments were carried out in the Geomicrobiology Laboratory of ETH Zürich using cultures of living microbes and artificial organic compounds that simulate functional groups present in natural biofilms formed under both aerobic and anaerobic conditions. In addition, pure inorganic experiments were designed to understand possible physico-chemical conditions for diagenetic processes that could induce dissolution of Mg-carbonates and precipitation of Mg-rich clays. Our results show a remarkable biotic influence during the formation of clay minerals. Specifically, extracellular polymeric substances (EPS), released by microbes in their

  8. CVD synthesis of carbon-based metallic photonic crystals

    CERN Document Server

    Zakhidov, A A; Baughman, R H; Iqbal, Z

    1999-01-01

    Three-dimensionally periodic nanostructures on the scale of hundreds of nanometers, known as photonic crystals, are attracting increasing interest because of a number of exciting predicted properties. In particular, interesting behavior should be obtainable for carbon- based structures having a dimensional scale larger than fullerenes and nanotubes, but smaller than graphitic microfibers. We show here how templating of porous opals by chemical vapor deposition (CVD) allows us to obtain novel types of graphitic nanostructures. We describe the synthesis of new cubic forms of carbon having extended covalent connectivity in three dimensions, which provide high electrical conductivity and unit cell dimensions comparable to optical wavelengths. Such materials are metallic photonic crystals that show intense Bragg diffraction. (14 refs).

  9. Bioleaching of incineration fly ash by Aspergillus niger – precipitation of metallic salt crystals and morphological alteration of the fungus

    OpenAIRE

    Tong-Jiang Xu; Thulasya Ramanathan; Yen-Peng Ting

    2014-01-01

    This study examines the bioleaching of municipal solid waste incineration fly ash by Aspergillus niger, and its effect on the fungal morphology, the fate of the ash particles, and the precipitation of metallic salt crystals during bioleaching. The fungal morphology was significantly affected during one-step and two-step bioleaching; scanning electron microscopy revealed that bioleaching caused distortion of the fungal hyphae (with up to 10 μm hyphae diameter) and a swollen pellet structure. I...

  10. Seasonal variations of dissolved organic carbon in precipitation over urban and forest sites in central Poland.

    Science.gov (United States)

    Siudek, Patrycja; Frankowski, Marcin; Siepak, Jerzy

    2015-07-01

    Spatial and temporal variability of carbon species in rainwater (bulk deposition) was studied for the first time at two sites located in urban area of Poznań City and protected woodland area (Jeziory), in central Poland, between April and December 2013. The mean concentration of total carbon (TC) for the first site was 5.86 mg L(-1), whereas for the second, 5.21 mg L(-1). Dissolved organic carbon (DOC) concentration accounted for, on average, 87 and 91 % of total carbon in precipitation at urban and non-urban sites, respectively. Significant changes in TC concentrations in rainwater were observed at both sites, indicating that atmospheric transformation, transport, and removal mechanisms of carbonaceous particles were affected by seasonal fluctuations in biogenic/anthropogenic emission and meteorological conditions (i.e., precipitation height and type, atmospheric transport). During the warm season, the DOC concentration in rainwater was mostly influenced by mixed natural and anthropogenic sources. In contrast, during the cold season, the DOC concentration significantly increased mainly as a result of anthropogenic activities, i.e., intensive coal combustion, domestic wood burning, high-temperature processes, etc. In addition, during the winter measurements, significant differences in mean DOC concentration (Kruskal-Wallis test, p urban and non-urban sites. These data imply that carbonaceous compounds are of crucial importance in atmospheric chemistry and should be considered as an important parameter while considering wet deposition, reactions with different substances, especially over polluted environments.

  11. Isolation and metagenomic characterization of bacteria associated with calcium carbonate and struvite precipitation in a pure moving bed biofilm reactor-membrane bioreactor.

    Science.gov (United States)

    Gonzalez-Martinez, A; Leyva-Díaz, J C; Rodriguez-Sanchez, A; Muñoz-Palazon, B; Rivadeneyra, A; Poyatos, J M; Rivadeneyra, M A; Martinez-Toledo, M V

    2015-01-01

    A bench-scale pure moving bed bioreactor-membrane bioreactor (MBBR-MBR) used for the treatment of urban wastewater was analyzed for the identification of bacterial strains with the potential capacity for calcium carbonate and struvite biomineral formation. Isolation of mineral-forming strains on calcium carbonate and struvite media revealed six major colonies with a carbonate or struvite precipitation capacity in the biofouling on the membrane surface and showed that heterotrophic bacteria with the ability to precipitate calcium carbonate and struvite constituted ~7.5% of the total platable bacteria. These belonged to the genera Lysinibacillus, Trichococcus, Comamomas and Bacillus. Pyrosequencing analysis of the microbial communities in the suspended cells and membrane biofouling showed a high degree of similarity in all the samples collected with respect to bacterial assemblage. The study of operational taxonomic units (OTUs) identified through pyrosequencing suggested that ~21% of the total bacterial community identified in the biofouling could potentially form calcium carbonate or struvite crystals in the pure MBBR-MBR system used for the treatment of urban wastewater.

  12. Concentration, sources and flux of dissolved organic carbon of precipitation at Lhasa city, the Tibetan Plateau

    Science.gov (United States)

    Li, C.

    2015-12-01

    Dissolved organic carbon (DOC) plays important role in climate system, but few data are available on the Tibetan Plateau (TP). In this study 89 precipitation samples were collected at Lhasa, the largest city of southern Tibet, from March to December 2013. The average concentration and wet deposition fluxes of DOC was 1.10 mg C/L and 0.62 g C m-2.yr-1, respectively. Seasonally, low DOC concentration and high flux appeared during monsoon period, which were in line with heavy precipitation amount, reflecting dilution effect of precipitation for the DOC. Compared to other regions, the values of Lhasa were lower than those of large cites (e.g. Beijing and Seoul) mainly because of less air pollution of Lhasa. The relationship between DOC and ion analysis showed that DOC of Lhasa was derived mainly from the natural sources, followed by burning activities. Furthermore, △14C value of DOC indicated that fossil combustion contributed around 20% of the precipitation DOC of Lhasa, indicating that the atmosphere of Lhasa has been influenced by vehicle emissions. Therefore, although atmosphere of Lhasa is relatively clean, pollutants emitted from local sources cannot be ignored.

  13. Effects of transformation temperature on VC interphase precipitation and resultant hardness in low-carbon steels

    International Nuclear Information System (INIS)

    The effects of transformation temperature on VC interphase precipitation in low-carbon steels were investigated mainly by using an Fe–0.1C–1.5Mn–0.4V–0.05Si (mass%) alloy isothermally transformed at different temperatures. The crystallographic relationship between ferrite and austenite as well as the precipitates and resultant hardness were characterized by combining electron backscatter diffraction, three-dimensional atom probe and nanoindentation measurements in the same ferrite grains. It was found that the number density of sheet-like interphase precipitation at non-K–S (Kurdjumov–Sachs) interfaces is significantly increased by decreasing the transformation temperature from 993 K to 923 K, while no great change can be obtained by further lowering the temperature to 873 K. The nanohardness of ferrite grains shows the same trend as that of VC number density. The effects of transformation temperature on VC interphase precipitation are discussed in terms of the driving force for VC nucleation. On the other hand, the temperature dependence of macroscopic hardness does not agree with that for nanohardness due to the fact that fraction of ferrite holding near the K–S orientation relationship with austenite changes substantially with transformation temperature

  14. Effect of Mg/Ca ratios on microbially induced carbonate precipitation

    Science.gov (United States)

    Balci, Nurgul; Demirel, Cansu; Seref Sonmez, M.; Kurt, M. Ali

    2016-04-01

    Influence of Mg/Ca ratios on microbially induced carbonate mineralogy were investigated by series of experiments carried out under various environmental conditions (Mg/Ca ratio, temperature and salinity). Halophilic bacterial cultures used for biomineralization experiments were isolated from hypersaline Lake Acıgöl (Denizli, SW Turkey), displaying extreme water chemistry with an average pH around 8.6 (Balci eta l.,2015). Enriched bacterial culture used in the experiments consisted of Halomonas saccharevitans strain AJ275, Halomonas alimentaria strain L7B; Idiomarina sp. TBZ29, 98% Idiomarina seosensis strain CL-SP19. Biomineralization experiments were set up using above enriched culture with Mg/Ca ratios of 0.05, 1, 4 and 15 and salinity of 8% and 15% experiments at 30oC and 10oC. Additionally, long-term biomineralization experiments were set up to last for a year, for Mg/Ca=4 and Mg/Ca=15 experiments at 30oC. For each experimental condition abiotic experiments were also conducted. Solution chemistry throughout incubation was monitored for Na, K, Mg, Ca, bicarbonate, carbonate, ammonium and phosphate for a month. At the end of the experiments, precipitates were collected and morphology and mineralogy of the biominerals were investigated and results were evaluated using the software DIFFRAC.SUITE EVA. Overall the preliminary results showed chemical precipitation of calcite, halite, hydromagnesite and sylvite. Results obtained from biological experiments indicate that, low Mg/Ca ratios (0.05 and 1) favor chlorapatite precipitation, whereas higher Mg/Ca ratios favor struvite precipitation. Biomineralization of dolomite, huntite and magnesite is favorable at high Mg/Ca ratios (4 and 15), in the presence of halophilic bacteria. Moreover, results indicate that supersaturation with respect to Mg (Mg/Ca=15) combined with NaCl (15%) inhibits biomineralization and forms chemical precipitates. 15% salinity is shown to favor chemical precipitation of mineral phases more than

  15. Enzyme precipitate coatings of glucose oxidase onto carbon paper for biofuel cell applications.

    Science.gov (United States)

    Fischback, Mike; Kwon, Ki Young; Lee, Inseon; Shin, Su Jeong; Park, Hyun Gyu; Kim, Byoung Chan; Kwon, Yongchai; Jung, Hee-Tae; Kim, Jungbae; Ha, Su

    2012-02-01

    Enzymatic biofuel cells (BFC) have a great potential as a small power source, but their practical applications are being hampered by short lifetime and low power density. This study describes the direct immobilization of glucose oxidase (GOx) onto the carbon paper in the form of highly stable and active enzyme precipitation coatings (EPCs), which can improve the lifetime and power density of BFCs. EPCs were fabricated directly onto the carbon paper via a three-step process: covalent attachment (CA), enzyme precipitation, and chemical crosslinking. GOx-immobilized carbon papers via the CA and EPC approaches were used as an enzyme anode and their electrochemical activities were tested under the BFC-operating mode. The BFCs with CA and EPC enzyme anodes produced the maximum power densities of 50 and 250 µW/cm(2) , respectively. The BFC with the EPC enzyme anode showed a stable current density output of >700 µA/cm(2) at 0.18 V under continuous operation for over 45 h. When a maple syrup was used as a fuel under ambient conditions, it also produced a stable current density of >10 µA/cm(2) at 0.18 V for over 25 h. It is anticipated that the direct immobilization of EPC on hierarchical-structured electrodes with a large surface area would further improve the power density of BFCs that can make their applications more feasible.

  16. Control on Crystal Forms of Ultrafine Barium Carbonate Particles and Study on its Mechanism

    Institute of Scientific and Technical Information of China (English)

    2005-01-01

    Barium carbonate particles were prepared by using homogeneous precipitation method and co-precipitation method respectively. Through adding different crystalline controlling modifiers, Barium carbonate particles in five different shapes including linear, needle-like, pillarlike, sphere-like and dumbbell-like were synthesized. These particles were characterized by SEM and XRD, and their synthetic mechanism was discussed in this paper.

  17. Experimental modelling of Calcium carbonate precipitation in the presence of phototrophic anaerobic bacteria Rhodovulum sp.

    Science.gov (United States)

    Bundeleva, Irina; Shirokova, Liudmila; Benezeth, Pascale; Pokrovsky, Oleg; Kompantseva, Elena

    2010-05-01

    Carbonate biomineralization is considered as one of the main natural processes controlling CO2 levels in the atmosphere both in the past and at present time. Haloalcaliphilic Rhodovulum sp. A-20s isolated from soda lake in southern Siberia and halophilic neutrophilic Rhodovulum sp. S-1765 isolated from hypersaline water body in Crimea steppe represent a large group of phototrophic bacteria likely to be involved in CaCO3 formation in soda and saline lakes. These bacteria use organic substrates for non-oxygenic photosynthesis and thus may mediate CaCO3 precipitation without CO2 consumption in highly-saline, highly-alkaline, NaHCO3-rich solutions. In order to provide the link between surface properties of bacteria and their ability to precipitate Ca carbonate, we used a combination of electrophoretic mobility measurements, surface titration and Ca ion adsorption using dead (autoclaved), inactivated (NaN3 - treated) and live cells at 25 °C as a unction of pH (3-11) and NaCl concentrations (0.01, 0.1, 0.5 M). Zeta potential of both bacteria is identical for active, NaN3-inactivated and dead cells at high ionic strength (0.5 M NaCl). The pH of isoelectric point is below 3 and zeta-potential decreases or remain negative up to pH 11. However, at lower ionic strength (0.1 M and 0.01 M NaCl) for live cells the potential increases towards positive values in the alkaline solutions (pH of 9 to 10). Similar to previous results on cyanobacteria (Martinez et al., 2009) there is a net increase in zeta-potential towards more positive values at pH = 10.4 for active cells. In order to better understand this phenomenon, experiments with different concentration of Ca2+ and HCO3- ions as well as experiments with live cultures in the darkness have been carried out. The presence in solution of Ca2+ (0.01 and 0.001 M) and the absence of light in experiment do not change significantly the potential of the cells. However, the presence in solution of HCO3- strongly reduces the zeta

  18. Bioleaching of incineration fly ash by Aspergillus niger – precipitation of metallic salt crystals and morphological alteration of the fungus

    Directory of Open Access Journals (Sweden)

    Tong-Jiang Xu

    2014-09-01

    Full Text Available This study examines the bioleaching of municipal solid waste incineration fly ash by Aspergillus niger, and its effect on the fungal morphology, the fate of the ash particles, and the precipitation of metallic salt crystals during bioleaching. The fungal morphology was significantly affected during one-step and two-step bioleaching; scanning electron microscopy revealed that bioleaching caused distortion of the fungal hyphae (with up to 10 μm hyphae diameter and a swollen pellet structure. In the absence of the fly ash, the fungi showed a linear structure (with 2–4 μm hyphae diameter. Energy-dispersive X-ray spectroscopy and X-ray diffraction confirmed the precipitation of calcium oxalate hydrate crystals at the surface of hyphae in both one-step and two-step bioleaching. Calcium oxalate precipitation affects bioleaching via the weakening of the fly ash, thus facilitating the release of other tightly bound metals in the matrix.

  19. Ellipsometric investigations of photonic crystals based on carbon nanofibers

    CERN Document Server

    Rehammar, R; Arwin, H; Kinaret, J M; Campbell, E E B

    2010-01-01

    Carbon nanofibers (CNF) are used as components of planar photonic crystals (PC). Square and rectangular lattices as well as random patterns of vertically aligned CNF were fabricated and their properties studied using ellipsometry. Conventional methods of ellipsometric analysis used in thin film ellipsometry are not applicable to these samples due to their nanostructured nature. We show that detailed information such as symmetry directions and the band structure of these novel materials can be extracted from considerations of the polarization state in the specular beam.

  20. The influence of xanthan on the crystallization of calcium carbonate

    Science.gov (United States)

    Yang, Xiaodeng; Xu, Guiying

    2011-01-01

    Calcium carbonate (CaCO 3) was crystallized in xanthan (XC) aqueous solutions. The CaCO 3 particles were characterized by scanning electron microscopy (SEM), powder X-ray diffraction (XRD), Fourier transform infrared (FTIR) spectroscopy and thermogravimetry analysis (TGA) methods. The concentrations of XC, Ca 2+ and CO 32- ions and the ratios [Ca 2+]/[CO 32-] and [Mg 2+]/[Ca 2+] show evident influence on the aggregation and growth of CaCO 3 particles. The presence of Mg 2+ ions influences not only the morphology, but also the polymorph of CaCO 3.

  1. Crystallization of Carbon Oxygen Mixtures in White Dwarf Stars

    CERN Document Server

    Horowitz, C J; Berry, D K

    2010-01-01

    We determine the phase diagram for dense carbon/ oxygen mixtures in White Dwarf (WD) star interiors using molecular dynamics simulations involving liquid and solid phases. Our phase diagram agrees well with predictions from Ogata et al. and Medin and Cumming and gives lower melting temperatures than Segretain et al. Observations of WD crystallization in the globular cluster NGC 6397 by Winget et al. suggest that the melting temperature of WD cores is close to that for pure carbon. If this is true, our phase diagram implies that the central oxygen abundance in these stars is less than about 60%. This constraint, along with assumptions about convection in stellar evolution models, limits the effective S factor for the $^{12}$C($\\alpha,\\gamma$)$^{16}$O reaction to S_{300} <= 170 keV barns.

  2. Characteristics of Particulate Carbon in Precipitation during the Rainy Season in Xiamen Island, China

    Directory of Open Access Journals (Sweden)

    Shuhui Zhao

    2016-10-01

    Full Text Available Measuring wet deposition of organic carbon (OC and elemental carbon (EC aerosol is crucial for the understanding of their circulation and climate effect. To further understand the wet deposition of particulate carbon (OC and EC, precipitation samples were collected from April to August 2014 on Xiamen Island in China. EC and water insoluble organic carbon (WIOC concentrations were analyzed using a thermal optical method to investigate temporal variations and wet deposition fluxes. The average EC and WIOC concentrations were 7.3 μgC·L−1 and 495.3 μgC·L−1, respectively, which are both comparable to the results reported in European areas. EC and WIOC concentrations were higher in spring than in summer. Higher EC concentrations were found in April, which were probably associated with the transport of air masses from northern continental areas. Higher WIOC concentrations were found in May and were mainly attributed to air masses from the South China Sea. Lower concentrations of EC and WIOC in the summer were primarily due to the clean air masses transported from the ocean. The wet deposition flux was calculated as the product of concentration and precipitation amount. Average wet deposition fluxes of EC and WIOC were estimated to be 0.6 mgC·m−2·month−1 and 36.7 mgC·m−2·month−1, respectively. Wet deposition fluxes of EC and WIOC exhibited similar concentration trends. The largest flux in EC wet deposition occurred in April (1.8 mgC·m−2·month−1, while the largest flux in WIOC wet deposition occurred in May (63.1 mgC·m−2·month−1.

  3. Stress–strain behavior of ferrite and bainite with nano-precipitation in low carbon steels

    International Nuclear Information System (INIS)

    We systematically investigate stress–strain behavior of ferrite and bainite with nano-sized vanadium carbides in low carbon steels; the ferrite samples were obtained through austenite/ferrite transformation accompanied with interphase precipitation and the bainite samples were via austenite/bainite transformation with subsequent aging. The stress–strain curves of both samples share several common features, i.e. high yield stress, relatively low work hardening and sufficient tensile elongation. Strengthening contributions from solute atoms, grain boundaries, dislocations and precipitates are calculated based on the structural parameters, and the calculation result is compared with the experimentally-obtained yield stress. The contributions from solute atoms and grain boundaries are simply additive, whereas those from dislocations and precipitates should be treated by taking the square root of the sum of the squares of two values. Nano-sized carbides may act as sites for dislocation multiplication in the early stage of deformation, while they may enhance dislocation annihilation in the later stage of deformation. Such enhanced dynamic recovery might be the reason for a relatively large elongation in both ferrite and bainite samples

  4. Biotic and abiotic effects on CO2 sequestration during microbially-induced calcium carbonate precipitation.

    Science.gov (United States)

    Okyay, Tugba Onal; Rodrigues, Debora F

    2015-03-01

    In this study, CO2 sequestration was investigated through the microbially-induced calcium carbonate precipitation (MICP) process with isolates obtained from a cave called 'Cave Without A Name' (Boerne, TX, USA) and the Pamukkale travertines (Denizli, Turkey). The majority of the bacterial isolates obtained from these habitats belonged to the genera Sporosarcina, Brevundimonas, Sphingobacterium and Acinetobacter. The isolates were investigated for their capability to precipitate calcium carbonate and sequester CO2. Biotic and abiotic effects of CO2 sequestration during MICP were also investigated. In the biotic effect, we observed that the rate and concentration of CO2 sequestered was dependent on the species or strains. The main abiotic factors affecting CO2 sequestration during MICP were the pH and medium components. The increase in pH led to enhanced CO2 sequestration by the growth medium. The growth medium components, on the other hand, were shown to affect both the urease activity and CO2 sequestration. Through the Plackett-Burman experimental design, the most important growth medium component involved in CO2 sequestration was determined to be urea. The optimized medium composition by the Plackett-Burman design for each isolate led to a statistically significant increase, of up to 148.9%, in CO2 uptake through calcification mechanisms. PMID:25764465

  5. Performance of separation processes for precipitated calcium carbonate produced with an innovative method from steelmaking slag and carbon dioxide

    Directory of Open Access Journals (Sweden)

    Sebastian eTeir

    2016-02-01

    Full Text Available In this work, experiments were performed to determine the filterability of calcium carbonate produced with an alternative calcium carbonate production concept. The concept uses steelmaking slag as raw material and has potential to fix CO2 emissions and utilize steelmaking slag, simultaneously. As calcium carbonate is precipitated in a solution containing ammonium chloride, calcium chloride and ammonia, the product needs to be washed and hence filtered. In this work different separation processes, including washing, filtering and drying, were tested on two calcium carbonate slurries produced from steel converter slag and CO2 by a laboratory-scale pilot facility, with the aim of obtaining a solid product with a low chloride content using a minimum amount of washing water. The order of maximum filtration rates achievable of the calcium carbonate slurries was determined by experimental work. The tests included pressure filtration and vacuum filtration and the test series contained altogether 21 different filtration cycles with varying combinations of filtering, washing, and drying steps. The filtered cakes were analyzed by their residual moisture content, chloride content and conductivity, and the filtrates by their residual solids content, chloride content and conductivity. Pressure filtration gave a high capacity (400-460 kg/m2h and a low cake residual moisture content (12-14 wt-%. Vacuum filtration gave slightly higher filtration rates (500-610 kg/m2h at the lowest residual chloride contents of the cakes, but the cake residual moisture also stayed higher (25-26 wt-%. As the vacuum filtration tests used a filter cloth with higher permeability than that of the pressure filtration tests, a slightly higher filtration rate was expected. However, both filtration technologies seem suitable for filtering and washing calcium carbonate prepared with the studied method as a residual chloride content as low as 10 ppm of the filtered solids can be achieved

  6. Preparation of Uranium Dioxide by Electrochemical Reduction in Ammonium Carbonate Solutions and Subsequent Precipitation

    International Nuclear Information System (INIS)

    Experiments in a small scale electrolysis cell on cathodic reduction of uranium (VI) to uranium (IV) show the possibility of an efficient way to obtain uranium (IV) in carbonate solutions. From this solution uranium (IV) hydrous oxide precipitates by merely raising the temperature. To obtain larger quantities of material needed for technological testing, a scale-up of the process was attempted. An electrolysis cell of hard PVC (polyvinylchloride) was constructed with a mercury pool cathode of approximately 2.5 dm2 and platinum anodes. The catholyte was separated from the anolyte by cationexchange membranes. The catholyte was circulated between two 50-1 reservoirs and streamed toward the vigorously stirred mercury cathode. The working potential of mercury was controlled against an Ag/AgCl/KC1 (sat.) reference electrode, the potential being held constant at -1.5 V. The current efficiency is approximately 90%; the power consumed for the reduction process is about 0.8 kWh/kg of uranium dioxide. After the electrolysis was completed the precipitation was initiated only by heating the deeply green clear solution up to 70 deg. C in a separate all-glass vessel of 60-1 volume. From 50, 1 of the catholyte solution 1 kg of a centrifuged product (containing about 20% of water) was obtained. The coulometric analysis of the oxygen-uranium ratio always gave results in the range of 2.04 to 2.09. By the procedure described uranium (IV) hydrous oxide is selectively precipitated, and the oxygen-uranium ratio in the precipitate was found to be independent of the degree of completion of the reduction. The product was identified as the alpha phase of uranium dioxide by the X-ray powder diffraction. Experiments in sintering and characterization of uranium dioxide thus obtained for the ceramic nuclear fuel requirements are under way. (author)

  7. Clumped isotope disequilibrium during rapid CO2 uptake and carbonate precipitation in subaerial alkaline springs associated with ongoing serpentinization

    Science.gov (United States)

    Falk, E. S.; Guo, W.; Kelemen, P. B.

    2014-12-01

    Ongoing serpentinization in tectonically exposed ultramafic bodies is manifested at the surface in alkaline springs (pH >11). Where these high-pH waters come in contact with CO2 at the surface, rapid calcite precipitation forms extensive travertines. We study natural travertine samples from Oman and synthetic witherite (BaCO3) from high-pH experiments to identify disequilibrium signals in δ18O, δ13C and clumped isotopes (measured as Δ47) that characterize rapid uptake of atmospheric CO2 and carbonate precipitation from high pH fluids. Kinetic effects preclude the use of clumped or oxygen isotopes for carbonate thermometry in these environments, but trends in δ18O, δ13C and Δ47 could help identify extinct alkaline systems or distinguish CO2 sources. Oman travertines formed at peridotite-hosted alkaline springs have long been known to exhibit a large range of kinetically depleted δ18O and δ13C values. We find fresh carbonate precipitated at these alkaline springs also exhibit large enrichments in Δ47 that covary with the depletions in δ18O and δ13C, thought to arise during hydroxylation of CO2 in high-pH fluids. Witherite precipitated during rapid CO2 uptake and carbonate precipitation in high pH experiments also exhibits disequilibrium values in δ18O, δ13C and Δ47, with the Δ47 of carbonate precipitates strongly affected by the Δ47 the reactant CO2. δ18O, δ13C and Δ47 trends could serve as a marker for carbonates formed in subaerial alkaline environments and track carbon sources in these systems. For example, the δ18O-δ13C slope in carbonates from Martian meteorites is similar to that observed in carbonates from terrestrial alkaline springs, so if corresponding enrichments in Δ47 could be identified in Martian carbonates, it could suggest that alkaline springs were present on the surface of Mars. Clumped isotope signals could also help distinguish carbon sources: kinetic enrichments in Δ47 would be absent or diminished in high-pH carbonates

  8. Impacts of Precipitation Diurnal Timing on Ecosystem Carbon Exchanges in Grasslands: A Synthesis of AmeriFlux Data

    Science.gov (United States)

    Song, X.; Xu, X.; Tweedie, C. E.

    2015-12-01

    Drylands have been found playing an important role regulating the seasonality of global atmospheric carbon dioxide concentrations. Precipitation is a primary control of ecosystem carbon exchanges in drylands where a large proportion of the annual total rainfall arrives through a small number of episodic precipitation events. While a large number of studies use the concept of "precipitation pulses" to explore the effects of short-term precipitation events on dryland ecosystem function, few have specifically evaluated the importance of the diurnal timing of these events. The primary goal of this study was to determine how the diurnal timing of rainfall events impacts land-atmosphere net ecosystem CO2 exchanges (NEE) and ecosystem respiration in drylands. Our research leverages a substantial and existing long-term database (AmeriFlux) that describes NEE, Reco and meteorological conditions at 11 sites situated in different dryland ecosystems in South West America. All sites employ the eddy covariance technique to measure land-atmosphere the CO2 exchange rates between atmosphere and ecosystem. Data collected at these sites range from 4 to 10 years, totaling up to 73 site-years. We found that episodic precipitation events stimulate not only vegetation photosynthesis but also ecosystem respiration. Specifically, the morning precipitation events decrease photosynthesis function at daytime and increase ecosystem respiration at nighttime; the afternoon precipitation events do not stimulate ecosystem photosynthesis at daytime, while stimulate ecosystem respiration; the night precipitations suppress photosynthesis at daytime, and enhance ecosystem respiration at nighttime.

  9. Sublimation properties in carbon containing tungsten-rhenium single crystals

    International Nuclear Information System (INIS)

    Data on sublimation parameters of W-Re single crystals with Re contents varying from 0.1 to 4.2 at % and different quantity of C, are obtained by the Langmuir method at superhigh vacuum. It is shown that the rates of sublimation in specimens with lesser carbon content (4.6X10-2 % at) increase with Re concentration growth (from 2.6 to 3.8% at) and sublimation parameters in specimens with greater carbon content (1.2x10-1 - 1.5x10-1% at) decrease in comparison with W(C=1.5x10-2 % at). The anisotropy of rate and heat of sublimation is observed in equivalent crystallographic directions , one of them is perpendicular to the crystallization direction. Another one - parallel to it. The effects observed are explained by the increase of C solubility in Re and by its redistribution in W bcc - lattice with a temperature increase

  10. Sublimation properties in carbon containing tungsten-rhenium single crystals

    Energy Technology Data Exchange (ETDEWEB)

    Dekhtyar, I.Ya.; Kolesnik, V.N.; Patoka, V.I.; Ovsienko, D.E.; Silant' ev, V.I.; Sosnina, E.I. (AN Ukrainskoj SSR, Kiev. Inst. Metallofiziki)

    Data on sublimation parameters of W-Re single crystals with Re contents varying from 0.1 to 4.2 at % and different quantity of C, are obtained by the Langmuir method at superhigh vacuum. It is shown that the rates of sublimation in specimens with lesser carbon content (4.6X10/sup -2/ % at) increase with Re concentration growth (from 2.6 to 3.8% at) and sublimation parameters in specimens with greater carbon content (1.2x10/sup -1/ - 1.5x10/sup -1/% at) decrease in comparison with W(C=1.5x10/sup -2/ % at). The anisotropy of rate and heat of sublimation is observed in equivalent crystallographic directions <100>, one of them is perpendicular to the crystallization direction. Another one - parallel to it. The effects observed are explained by the increase of C solubility in Re and by its redistribution in W bcc - lattice with a temperature increase.

  11. Atom probe tomography of secondary γ′ precipitation in a single crystal Ni-based superalloy after isothermal aging at 1100 °C

    Energy Technology Data Exchange (ETDEWEB)

    Tan, X.P., E-mail: xptan1985@gmail.com [IM 2NP, UMR 7334 CNRS, Université Aix-Marseille, 13397 Marseille Cedex 20 (France); Mangelinck, D.; Perrin-Pellegrino, C. [IM 2NP, UMR 7334 CNRS, Université Aix-Marseille, 13397 Marseille Cedex 20 (France); Rougier, L. [LSMX, MXG, Ecole Polytechnique Fédérale de Lausanne, 1015 Lausanne (Switzerland); Gandin, Ch.-A. [CEMEF, UMR 7635 CNRS, MINES ParisTech, 06904 Sophia Antipolis (France); Jacot, A. [LSMX, MXG, Ecole Polytechnique Fédérale de Lausanne, 1015 Lausanne (Switzerland); Ponsen, D.; Jaquet, V. [Snecma-SAFRAN Group, Service YQGC, 92702 Colombes (France)

    2014-10-25

    Highlights: • Bimodal size distribution of γ′ precipitates occurs after isothermal aging at 1100 °C. • Characterization of secondary γ′ by atom probe tomography. • It is proposed that the secondary γ′ occurs via a non-classical nucleation. • The coarsening of secondary γ′ precipitates well obeys the classical LSW theory. - Abstract: Secondary γ′ precipitation in a commercial single crystal Ni-based superalloy after the 1100 °C isothermal aging has been investigated by atom probe tomography. After the isothermal aging for 300 s, 1800 s and 3600 s, a bimodal size distribution of larger primary γ′ precipitates and numerous smaller secondary γ′ precipitates was obtained. It is proposed that the secondary γ′ precipitated via a non-classical nucleation mode. The coarsening of secondary γ′ precipitates well obeys the classical LSW theory.

  12. Study of Crystallization Process during La and La2(CO3)3 Precipitation with Sodium Bicarbonate%碳酸氢钠沉淀镧及碳酸镧的结晶过程研究

    Institute of Scientific and Technical Information of China (English)

    焦小燕; 罗贤满; 杨宇俊; 辜子英; 李永绣

    2001-01-01

    Based on pH situ-determination data,together with the results of variation in precipitation volume and precipitation partical size,the properties of lanthanum carbonate precipitated with sodium bicarbonate were investigated.The results show that crystalliazation active zone of lanthanum carbonate is in low molar ratio zone,where the moalr ratio is between 0.541~2.828.However,the crystallization of lanthanum carbonate in high molar ratio zone is inactive.At the same tine,the influence of stirring on the crystallization of lanthanum carbonate was examined ,the crystallization mechanism was discussed and the corresponding reaction equations were proposed.%以pH值原位测定法为基础,结合沉淀体积变化、沉淀粒度及外观形貌分析结果,对NaHCO3沉淀镧的性能及碳酸镧的结晶过程进行了研究。结果表明:碳酸镧结晶活性区域位于低配比区0.541~2.828之间,而在高配比区其结晶是惰性的。同时还考察了搅拌对结晶过程的影响,讨论了NaHCO3沉淀镧时的沉淀反应和结晶化机理。并给出了相关的化学反应方程式。

  13. Influence of precipitating agents on thermodynamic parameters of protein crystallization solutions.

    Science.gov (United States)

    Stavros, Philemon; Saridakis, Emmanuel; Nounesis, George

    2016-09-01

    X-ray crystallography is the most powerful method for determining three-dimensional structures of proteins to (near-)atomic resolution, but protein crystallization is a poorly explained and often intractable phenomenon. Differential Scanning Calorimetry was used to measure the thermodynamic parameters (ΔG, ΔH, ΔS) of temperature-driven unfolding of two globular proteins, lysozyme, and ribonuclease A, in various salt solutions. The mixtures were categorized into those that were conducive to crystallization of the protein and those that were not. It was found that even fairly low salt concentrations had very large effects on thermodynamic parameters. High concentrations of salts conducive to crystallization stabilized the native folded forms of proteins, whereas high concentrations of salts that did not crystallize them tended to destabilize them. Considering the ΔH and TΔS contributions to the ΔG of unfolding separately, high concentrations of crystallizing salts were found to enthalpically stabilize and entropically destabilize the protein, and vice-versa for the noncrystallizing salts. These observations suggest an explanation, in terms of protein stability and entropy of hydration, of why some salts are good crystallization agents for a given protein and others are not. This in turn provides theoretical insight into the process of protein crystallization, suggesting ways of predicting and controlling it. © 2016 Wiley Periodicals, Inc. Biopolymers 105: 642-652, 2016. PMID:27114109

  14. Promising dissolution enhancement effect of soluplus on crystallized celecoxib obtained through antisolvent precipitation and high pressure homogenization techniques.

    Science.gov (United States)

    Homayouni, Alireza; Sadeghi, Fatemeh; Varshosaz, Jaleh; Afrasiabi Garekani, Hadi; Nokhodchi, Ali

    2014-10-01

    Poor solubility and dissolution of hydrophobic drugs have become a major challenge in pharmaceutical development. Drug nanoparticles have been widely accepted to overcome this problem. The aim of this study was to manufacture celecoxib nanoparticles using antisolvent precipitation and high pressure homogenization techniques in the presence of varying concentrations of soluplus(®) as a hydrophilic stabilizer. Antisolvent crystallization followed by freeze drying (CRS-FD) and antisolvent crystallization followed by high pressure homogenization and freeze drying (HPH-FD) were used to obtain celecoxib nanoparticles. The obtained nanoparticles were analyzed in terms of particle size, saturation solubility, morphology (optical and scanning electron microscopy), solid state (DSC, XRPD and FT-IR) and dissolution behavior. The results showed that celecoxib nanoparticle can be obtained when soluplus was added to the crystallization medium. In addition, the results showed that the concentration of soluplus and the method used to prepare nanoparticles can control the size and dissolution of celecoxib. Samples obtained in the presence of 5% soluplus through HPH technique showed an excellent dissolution (90%) within 4min. It is interesting to note that celecoxib samples with high crystallinity showed better dissolution than those celecoxib samples with high amorphous content, although they had the same concentration of soluplus. DSC and XRPD proved that samples obtained via HPH technique are more crystalline than the samples obtained through only antisolvent crystallization technique. PMID:25124835

  15. Mechanistic Study of Magnesium Carbonate Semibatch Reactive Crystallization with Magnesium Hydroxide and CO2

    DEFF Research Database (Denmark)

    Han, B.; Qu, H. Y.; Niemi, H.;

    2014-01-01

    This work investigates semibatch precipitation of magnesium carbonate at ambient temperature and pressure using Mg(OH)(2) and CO2 as starting materials. A thermal analysis method was developed that reflects the dissolution rate of Mg(OH)(2) and the formation of magnesium carbonate. The method...... the liquid and solid phases. A stirring rate of 650 rpm was found to be the optimum speed as the flow rate of CO2 was 1 L/min. Precipitation rate increased with gas flow rate, which indicates that mass transfer of CO2 plays a critical role in this precipitation case. Magnesium carbonate trihydrate...

  16. Morphology and Precipitation Kinetics of MnS in Low-Carbon Steel During Thin Slab Continuous Casting Process

    Institute of Scientific and Technical Information of China (English)

    YU Hao; KANG Yong-lin; ZHAO Zheng-zhi; SUN Hao

    2006-01-01

    The morphology of manganese sulfide formed during thin slab continuous casting process in low-carbon steel produced by compact strip production (CSP) technique was investigated. Using transmission electron microscopy analysis, it was seen that a majority of manganese sulfides precipitated at austenite grain boundaries, the morphologies of which were spherical or close to the spherical shape and the size of MnS precipitates ranged from 30 nm to 100 nm. A mathematical model of the manganese sulfide precipitation in this process was developed based on classical nucleation theory. Under the given conditions, the starting and finishing precipitation temperatures of MnS in the continuous casting thin slab of the studied low-carbon steel are 1 189 ℃ and 1 171 ℃, respectively, and the average diameter of MnS precipitates is about 48 nm within this precipitation temperature range. The influences of chemical components and thermo-mechanical processing conditions on the precipitation behavior of MnS in the same process were also discussed.

  17. Influence of acid-soluble proteins from bivalve Siliqua radiata ligaments on calcium carbonate crystal growth

    Science.gov (United States)

    Huang, Zeng-Qiong; Zhang, Gang-Sheng

    2016-08-01

    In vitro biomimetic synthesis of calcium carbonate (CaCO3) in the presence of shell proteins is a heavily researched topic in biomineralization. However, little is known regarding the function of bivalve ligament proteins in the growth of CaCO3 crystals. In this study, using fibrous protein K58 from Siliqua radiata ligaments or coverslips as substrates, we report the results of our study of CaCO3 precipitation in the presence or absence of acid-soluble proteins (ASP) from inner ligament layers. ASP can disturb the controlling function of K58 or a coverslip on the crystalline phase, resulting in the formation of aragonite, calcite, and vaterite. In addition, we identified the following four primary components from ASP by mass spectroscopy: alkaline phosphatase (ALP), ABC transporter, keratin type II cytoskeletal 1 (KRT 1), and phosphate ABC transporter, phosphate-binding protein (PstS). Further analysis revealed that the first three proteins and especially ALP, which is important in bone mineralisation, could affect the polymorphism and morphology of CaCO3 crystals by trapping calcium ions in their domains. Our results indicate that ALP may play an important role in the formation of aragonite in S. radiata ligaments. This paper may facilitate our understanding of the biomineralization process.

  18. Carbonate precipitation in brine – a potential trigger for tropospheric ozone depletion events

    Directory of Open Access Journals (Sweden)

    R. Sander

    2006-01-01

    Full Text Available Tropospheric ozone depletion events (ODEs at high latitudes were discovered 20 years ago and are attributed to bromine explosions. However, an unresolved issue is the explanation of how the acid-catalyzed reaction cycle is triggered in atmospheric particles derived from alkaline sea water. By simulating the chemistry occuring in polar regions over recently formed sea ice, we can model successfully the transformation of inert sea-salt bromide to reactive bromine monoxide (BrO and the subsequent ODE when precipitation of calcium carbonate from freezing sea water is taken into account. In addition, we found the temperature dependence of the equilibrium BrCl+Br−↔Br2Cl− to be important.

  19. Effect of precipitated calcium carbonate--Cellulose nanofibrils composite filler on paper properties.

    Science.gov (United States)

    He, Ming; Cho, Byoung-Uk; Won, Jong Myoung

    2016-01-20

    A new concept of composite filler was developed by using cellulose nanofibrils (CNF), precipitated calcium carbonate (PCC) and cationic starch (C-starch). In this study, cellulose nanofibrils were utilized in two different ways: a PCC-CNF composite filler and a papermaking additive in sheet forming. The aim was to elucidate their effects on flocculation, filler retention and the strength and optical properties of handsheets. The highest filler retention was obtained by using the PCC-CNF composite filler in paper sheets. The paper filled with the composite fillers had much higher bursting and tensile strengths than conventional PCC loading. It was also found that the paper prepared with PCC-CNF composite fillers became denser with increasing the filler content of paper.

  20. NbC precipitates EELS spectra in a very low carbon microalloyed steel

    Directory of Open Access Journals (Sweden)

    Mancilla, J. E.

    2004-06-01

    Full Text Available In this paper a characterization study by transmission electron microscopy (TEM and electron energy loss spectroscopy (EELS of NbC precipitates in microalloyed steel is presented. The steel was hot rolled in a laboratory scale two-high reversing mill. The shape, size, location, and number of particles per unit area in the steel microstructure are reported. The particles were semi quantitatively analyzed for the heavier alloying elements using EDS, while EELS was used for the lighter elements, e. g. carbon and nitrogen. The EELS study of the precipitates reveals that the carbon is present as a compound (NbC without nitrogen.

    En este trabajo se presenta un estudio de caracterización por espectroscopia de pérdida de energía de electrones (EPEE realizado en un microscopio electrónico de transmisión de los precipitados de NbC en un acero microaleado. El acero se laminó en caliente en un laminador dúo reversible escala laboratorio. Las partículas de precipitados se caracterizaron en tamaños, formas y distribución y se analizaron semicuantitativamente para los elementos de aleación del acero más pesados, empleando un detector por dispersión de energías de rayos X, mientras que la EPEE se empleó para los elementos más ligeros, es decir, el carbono y el nitrógeno. El estudio por EPEE de los precipitados muestra que el carbono está presente como un compuesto (NbC sin que se haya encontrado nitrógeno en los mismos.

  1. Ca-carbonates precipitation and limestone genesis — the microbiogeologist point of view

    Science.gov (United States)

    Castanier, Sabine; Le Métayer-Levrel, Gaële; Perthuisot, Jean-Pierre

    1999-07-01

    Experiments show that the production of carbonate particles by heterotrophic bacteria follows different ways. In heterotrophy, the passive carbonatogenesis is generated by modifications of the medium that lead to the accumulation of carbonate and bicarbonate ions and to the precipitation of solid particles. It is induced by several metabolic pathways of the nitrogen cycle (ammonification of amino-acids, degradation of urea and uric acid, dissimilatory reduction of nitrates) and of the sulphur cycle (dissimilatory reduction of sulphates). The active carbonatogenesis is independent of the mentioned metabolic pathways. The carbonate particles are produced by ionic exchanges through the cell membrane following still poorly known mechanisms. In autotrophy, non-methylotrophic methanogenesis and cyanobacterial photosynthesis also may contribute to the precipitation of carbonates (autotrophic carbonates). As carbonatogenesis is neither restricted to particular taxonomic groups of bacteria nor to specific environments, it has been an ubiquitous phenomenon since Precambrian times. Carbonatogenesis is the response of heterotrophic bacterial communities to an enrichment of the milieu in organic matter. After a phase of latency, there is an exponential increase of bacterial numbers together with the accumulation of metabolic end-products. These induce a pH increase and an accumulation of carbonate and hydrogenocarbonate ions in the medium. This phase ends into a steady state when most part of the initial enrichment is consumed and there is a balance between death and growth in bacterial populations. Particulate carbonatogenesis occurs during the exponential phase and ends more or less after the beginning of the steady state. The active carbonatogenesis seems to start first and to be followed by the passive one which induces the growth of initially produced particles. In eutrophic conditions, the first solid products are patches that appear on the surface of the bacterial bodies

  2. Seeding Experiment of Liquid Carbon Dioxide for Enhancing Winter-time Precipitation in Saga Prefecture,Northern Kyushu,Japan

    Science.gov (United States)

    Wakimizu, K.; Nishiyama, K.; Tomine, K.; Maki, T.; Suzuki, Y.; Morita, O.

    2012-12-01

    Many droughts (shortage of water) have broken out by extreme small amount rainfall in recent Japan. So far,in order to prevent these droughts,artificial rainfall methods with 'AgI' or 'dry ice' have been widely used in Japan. However,these methods have many problems,which a large amount of overcooling liquid in the cumulus cloud was not able to be converted into precipitation efficiently. So as to solve these problems,new artificial rainfall method using liquid carbon dioxide (LC) was proposed by Fukuta (1996). This new method consists of the generation of ice particles by homogeneous nucleation using LC and the subsequent more effective growth for ice particles without competition process. And, this method is called 'Low-Level Penetration Seeding of Homogeneous Ice Nucleant (LOLEPSHIN)' ; this induces a 'Roll-up Expansion of Twin Horizontal Ice-crystal Thermals (RETHIT)' and a subsequent 'Falling growth-Induced Lateral Air Spreading (FILAS)'. This LC method was applied to thin super-cooled cumulus clouds in Saga prefecture, Northern Kyushu, Japan on February 4,2006. The seeding airplane took off the Atugi Airport in Kanagawa Prefecture toward the Iki Island around 0830JST. Many cloud bands were cofirmed in the flight going to the experimental area and the cloud base temperature was approximately -9C (1200m). Scince some young developing thin cumuli were found over the Iki Island, LC seeding to these clouds was carried out two times from 0841JST until 0919JST penetrating the -9C (1200m) altitude. The first precipitation seeding ebded in failure. The second penetration seeding was done for 115 seconds around 0917JST. This penetration led to success of developing one artificial echo (Echo I) in the leeward side of the Iki Island. Eco I moved from NNW to SSW. The maximum area of Echo I were 48km2 (at 1033JST) and first comfirmed by the Kyushu University radar (KU radar) at 1006JST (46 min. after LC seeding) around Mt.Sefuri in Saga Prefecture. It can be inferred that

  3. Analyzing carbon losses from dry soils after precipitation pulses by stable carbon isotopes

    Science.gov (United States)

    Unger, Stephan; Máguas, Cristina; Santos-Pereira, João.; Werner, Christiane

    2010-05-01

    Rain events after drought periods strongly increase soil respiration (Birch effect) and affect plant activity, and thus, may influence the isotopic signal of ecosystem respiration. These CO2-pulses may largely affect the C-balance of arid and semi-arid systems. Here, we evaluate the origins of the Birch effect in a Mediterranean forest and its influence on the isotopic signal of ecosystem (δ13CR) and soil respiration (δ13CSoil). We conducted artificial rain pulses in May and August 2005 and estimated δ13CSoil on intact vegetation, bare and root-free soil in response to watering. After watering in May δ13CSoil showed strong enrichment (-18) and a rapid return to initial values (-27). This transient enrichment was smaller in August than in May (ca. -22). Further, we compared δ13CR and δ13CSoil after first natural rains in October 2005, where both revealed a good relationship over the diurnal and the fortnight cycle. We hypothesize that the 'Birch effect' immediately after irrigation is the result of a hypo-osmotic stress response of the soil microbial community: during sudden moisture changes enriched osmoregulants are rapidly released and mineralized by the soil microbes to avoid cell lysis. After the pulse soil respiration followed a common moisture response. The overall impact of the Birch effect on C-sequestration will depend on both timing and frequency of the rains and thus, on whether the respired CO2 source is microbial or soil organic matter carbon.

  4. Carbon Mineralization by Aqueous Precipitation for Beneficial Use of CO2 from Flue Gas

    Energy Technology Data Exchange (ETDEWEB)

    Brent Constantz; Randy Seeker; Martin Devenney

    2010-06-30

    Calera's innovative Mineralization via Aqueous Precipitation (MAP) technology for the capture and conversion of CO{sub 2} to useful materials for use in the built environment was further developed and proven in the Phase 1 Department of Energy Grant. The process was scaled to 300 gallon batch reactors and subsequently to Pilot Plant scale for the continuous production of product with the production of reactive calcium carbonate material that was evaluated as a supplementary cementitious material (SCM). The Calera SCM{trademark} was evaluated as a 20% replacement for ordinary portland cement and demonstrated to meet the industry specification ASTM 1157 which is a standard performance specification for hydraulic cement. The performance of the 20% replacement material was comparable to the 100% ordinary portland cement control in terms of compressive strength and workability as measured by a variety of ASTM standard tests. In addition to the performance metrics, detailed characterization of the Calera SCM was performed using advanced analytical techniques to better understand the material interaction with the phases of ordinary portland cement. X-ray synchrotron diffraction studies at the Advanced Photon Source in Argonne National Lab confirmed the presence of an amorphous phase(s) in addition to the crystalline calcium carbonate phases in the reactive carbonate material. The presence of carboaluminate phases as a result of the interaction of the reactive carbonate materials with ordinary portland cement was also confirmed. A Life Cycle Assessment was completed for several cases based on different Calera process configurations and compared against the life cycle of ordinary portland cement. In addition to the materials development efforts, the Calera technology for the production of product using an innovative building materials demonstration plant was developed beyond conceptual engineering to a detailed design with a construction schedule and cost estimate.

  5. Controlling the number of walls in multi walled carbon nanotubes/alumina hybrid compound via ball milling of precipitate catalyst

    Energy Technology Data Exchange (ETDEWEB)

    Nosbi, Norlin [School of Materials and Mineral Resources Engineering, Engineering Campus, Universiti Sains Malaysia (USM), 14300 Nibong Tebal, Seberang Perai Selatan, Pulau Pinang (Malaysia); Akil, Hazizan Md, E-mail: hazizan@usm.my [School of Materials and Mineral Resources Engineering, Engineering Campus, Universiti Sains Malaysia (USM), 14300 Nibong Tebal, Seberang Perai Selatan, Pulau Pinang (Malaysia); Cluster for Polymer Composite (CPC), Science and Engineering Research Centre, Engineering Campus, Universiti Sains Malaysia (USM), 14300 Nibong Tebal, Seberang Perai Selatan, Pulau Pinang (Malaysia)

    2015-06-15

    Graphical abstract: - Highlights: • We report that, to manipulate carbon nanotubes geometry and number of walls are by controlling the precipitate catalyst size. • Number of walls and geometry effects depend on the milling time of the precipitate catalyst. • Increasing milling of time will decrease the carbon nanotubes number of walls. • Increasing milling of time will increase the carbon nanotubes thermal conductivity. - Abstract: This paper reports the influence of milling time on the structure and properties of the precipitate catalyst of multi walled carbon nanotubes (MWCNT)/alumina hybrid compound, produced through the chemical vapour deposition (CVD) process. For this purpose, light green precipitate consisted of aluminium, nickel(II) nitrate hexahydrate and sodium hydroxide mixture was placed in a planetary mill equipped with alumina vials using alumina balls at 300 rpm rotation speed for various milling time (5–15 h) prior to calcinations and CVD process. The compound was characterized using various techniques. Based on high-resolution transmission electron microscopy analysis, increasing the milling time up to 15 h decreased the diameter of MWCNT from 32.3 to 13.1 nm. It was noticed that the milling time had a significant effect on MWCNT wall thickness, whereby increasing the milling time from 0 to 15 h reduced the number of walls from 29 to 12. It was also interesting to note that the carbon content increased from 23.29 wt.% to 36.37 wt.% with increasing milling time.

  6. Modeling effects of temperature and precipitation on carbon characteristics and GHGs emissions in Abies fabric forest of subalpine

    Institute of Scientific and Technical Information of China (English)

    LU Xuyang; CHENG Genwei; XIAO Feipeng; FAN Jihui

    2008-01-01

    Abies fabric forest in the eastern slope of Gongga mountain is one type of subalpine dark coniferous forests of southwestern China.It is located on the southeastern edge of the Qinghai-Tibet plateau and is sensitive to climatic changes,A process-oriented biogeochemical model,Forest-DNDC,was applied to simulate the effects of climatic factors,temperature and precipitation changes on carbon characteristics,and greenhouse gases (GHGs) emissions inA.fabric forest.Validation indicated that the Forest-DNDC could be used to predict carbon characteristics and GHGs emissions with reasonable accuracy.The model simulated carbon fluxes,soil carbon dynamics,soil CO2,N2O,and NO emissions with the changes of temperature and precipitation conditions.The results showed that with variation in the baseline temperature from-2℃ to+2℃,the gross primary production (GPP) and soil organic carbon (SOC)increased,and the net primary production (NPP) and net ecosystem production (NEP) decreased because of higher respiration rate.With increasing baseline precipitation the GPP and NPP increased slightly,and the NEP and SOC showed decreasing trend.Soil CO2 emissions increased with the increase of temperature,and CO2 emissions changed little with increased baseline precipitation.With increased temperature and decreased baseline temperature,the total annual soil N2O emissions increased.With the variation of baseline temperature from -2℃ to +2℃,the total annual soil NO emissions increased.The total annual N2O and NO emissions showed increasing trends with the increase of precipitation.The biogeochemical simulation of the typical forest indicated that temperature changes strongly affected carbon fluxes,soil carbon dynamics,and soil GHGs emissions.The precipitation was not a principal factor affecting carbon fluxes,soil carbon dynamics,and soil CO2 emissions,but changes in precipitation could exert strong effect on soil N2O and NO emissions.

  7. Geochemical modeling of the influence of silicate mineral alteration on alkalinity production and carbonate precipitation

    Science.gov (United States)

    Herda, Gerhard; Kraemer, Stephan M.; Gier, Susanne; Meister, Patrick

    2016-04-01

    High CO2 partial pressure (pCO2) in deep rock reservoirs causes acidification of the porefluid. Such conditions occur during injection and subsurface storage of CO2 (to prevent the release of greenhouse gas) but also naturally in zones of strong methanogenic microbial activity in organic matter-rich ocean margin sediments. The acidic fluids are corrosive to carbonates and bear the risk of leakage of CO2 gas to the surface. Porefluid acidification may be moderated by processes that increase the alkalinity, i.e. that produce weak acid anions capable of buffering the acidification imposed by the CO2. Often, alkalinity increases as a result of anaerobic microbial activity, such as anaerobic oxidation of methane. However, on a long term the alteration of silicates, in particular, clay minerals, may be a more efficient mechanism of alkalinity production. Under altered temperature, pressure and porefluid composition at depth, clay minerals may change to thermodynamically more stable states, thereby increasing the alkalinity of the porefluid by partial leaching of Mg-(OH)2 and Ca-(OH)2 (e.g. Wallmann et al., 2008; Mavromatis et al., 2014). This alteration may even be enhanced by a high pCO2. Thus, silicate alteration can be essential for a long-term stabilization of volatile CO2 in the form of bicarbonate or may even induce precipitation of carbonate minerals, but these processes are not fully understood yet. The goal of this study is to simulate the alkalinity effect of silicate alteration under diagenetic conditions and high pCO2 by geochemical modeling. We are using the program PHREEQC (Parkhurst and Appelo, 2013) to generate high rock/fluid ratio characteristics for deep subsurface rock reservoirs. Since we are interested in the long-term evolution of diagenetic processes, over millions of years, we do not consider kinetics but calculate the theoretically possible equilibrium conditions. In a first step we are calculating the saturation state of different clay minerals

  8. Boron isotopic fractionation in laboratory inorganic carbonate precipitation: Evidence for the incorpora-tion of B(OH)3 into carbonate

    Institute of Scientific and Technical Information of China (English)

    2008-01-01

    A laboratory inorganic carbonate precipitation experiment at high pH of 8.96 to 9.34 was conducted, and the boron isotopic fractionations of the precipitated carbonate were measured. The data show that boron isotopic fractionation factors (αcarb-3) between carbonate and B(OH)3 in seawater range 0.937 and 0.965, with an average value of 0.953. Our results together with those reported by Sanyal and collabo-rators show that the αcarb-3 values between carbonate and B(OH)3 in solution are not constant but are negatively correlated with the pH of seawater. The measured boron isotopic compositions of carbonate precipitation (δ11Bcarb) do not exactly lie on the best-fit theoretical δ 11B4-pH curves and neither do they exactly parallel any theoretical δ 11B4-pH curves. Therefore, it is reasonable to argue that a changeable proportion of B(OH)3 with pH of seawater should also be incorporated into carbonate except for the dominant incorporation of B(OH)4- in carbonate . Hence, in the reconstruction of the paleo-pH of sea-water from boron isotopes in marine biogenic carbonates, the use of theoretical boron isotopic frac-tionation factor (α4-3) between B(OH)4- and B(OH)3 is not suitable. Instead, an empirical equation should be established.

  9. Adsorption properties of carbonized polyacrylonitrile deposited on {gamma}-alumina and silica gel by precipitation polymerization

    Energy Technology Data Exchange (ETDEWEB)

    Kustrowski, Piotr, E-mail: kustrows@chemia.uj.edu.pl [Faculty of Chemistry, Jagiellonian University, Ingardena 3, 30-060 Krakow (Poland); Janus, Rafal; Kochanowski, Andrzej; Chmielarz, Lucjan; Dudek, Barbara; Piwowarska, Zofia [Faculty of Chemistry, Jagiellonian University, Ingardena 3, 30-060 Krakow (Poland); Michalik, Marek [Institute of Geological Sciences, Jagiellonian University, Oleandry 2a, 30-063 Krakow (Poland)

    2010-07-15

    The precipitation polymerization method was used for the deposition of various contents of polyacrylonitrile on two oxide-type supports ({gamma}-alumina and silica gel). The synthesized materials were characterized by thermal analysis performed in inert and oxidizing atmospheres. The mechanism of polyacrylonitrile decomposition was proposed. In order to gain effective adsorbents of volatile organic compounds the polyacrylonitrile/support composites were carbonized at elevated temperatures. The texture and morphology of the calcined materials were examined by low-temperature sorption of N{sub 2} and scanning electron microscopy, respectively. An influence of thermal treatment conditions and carbonaceous species loading on adsorption capacity of methyl-ethyl ketone vapour was also determined. Attenuated total reflection Fourier transform infrared spectroscopy measurements revealed that the ladder-type polyacrylonitrile species formed above 250 {sup o}C and stable up to about 350-400 {sup o}C are the most effective sites for methyl-ethyl ketone sorption. The carbonaceous species dispersion was found to be an additional factor influencing the adsorption capacity of the carbonized polyacrylonitrile/support composites.

  10. Capillarity creates single-crystal calcite nanowires from amorphous calcium carbonate.

    Science.gov (United States)

    Kim, Yi-Yeoun; Hetherington, Nicola B J; Noel, Elizabeth H; Kröger, Roland; Charnock, John M; Christenson, Hugo K; Meldrum, Fiona C

    2011-12-23

    Single-crystal calcite nanowires are formed by crystallization of morphologically equivalent amorphous calcium carbonate (ACC) particles within the pores of track etch membranes. The polyaspartic acid stabilized ACC is drawn into the membrane pores by capillary action, and the single-crystal nature of the nanowires is attributed to the limited contact of the intramembrane ACC particle with the bulk solution. The reaction environment then supports transformation to a single-crystal product.

  11. Calcium Carbonate Crystal Growth in Porous Media, in the presence of Water Miscible and Non-Miscible Organic Fluids

    Science.gov (United States)

    Jaho, Sofia; Sygouni, Varvara; Paraskeva, Christakis A.

    2015-04-01

    The deposition of sparingly soluble salts (scaling) within porous media is a major problem encountered in many industrial and environmental applications. In the oil industry scaling causes severe operational malfunctions and, therefore, increasing the total operating and maintenance cost [1]. The most common types of sparingly soluble salts located in oil fields include carbonate and sulfate salts of calcium, strondium and barium[1,2]. Multiple phase flow and tubing surface properties are some of the factors affecting scale formation [3]. The main purpose of the present work was the investigation of the precipitation mechanisms of calcium carbonate (CaCO3) through in situ mixing of two soluble salt solutions in a flow granular medium, in the presence of water miscible organic fluid (ethylene glycol) or non-miscible organic fluid (n-dodecane). All series of experiments were carried out in a two dimensional porous medium made of Plexiglas. For all solutions used in the experiments, the contact angles with the surface of the porous medium and the interfacial tensions were measured. During the experiments, the calcium carbonate crystal growth was continuously monitored and recorded through an optical microscope equipped with a digital programmed video camera. The snap-shots were taken within specific time intervals and their detailed procession gave information concerning the crystal growth rate and kinetics. The pH of the effluent was measured and fluids samples were collected for calcium analysis using Atomic Absorption Spectroscopy (AAS). In all experiments effluent calcium concentration decreased as a function of time, suggesting that CaCO3 precipitation took place inside the porous medium. Crystals of the precipitated salt were identified using Infrared Spectroscopy (IR) and the morphology of the crystals was examined using Scanning Electron Microscopy (SEM). The induction time for precipitation of CaCO3 crystals in the presence of n-dodecane was significantly

  12. Synthesis and Characterisation of Struvite Family Crystals by An Aqueous Precipitation Method

    Directory of Open Access Journals (Sweden)

    Sutiyono S.

    2016-01-01

    Full Text Available Struvite (NH4MgPO4•6H2O is a mineral often found as a scale deposit in an industrial process and piping. The common occurrence of struvite formation is a wide variety of environments. pH solution and environmental temperature are important parameters that control precipitation and subsequent decomposition of struvite. The study aims to characterise the struvite precipitated out the solution through chemical and mineralogical analysis. In this work, struvite solution was prepared by mixing NH4OH , MgCl2 and H3PO4 with the different purity grade (A and B in the mol ratio of 1 : 1 : 1 in the stirred glass vessel tank with volume of 500 ml, and then stirred at 200 rpm for 70 minutes. Temperature of 3°C and an initial pH of 10 were selected. The precipitated deposit was dried at room temperature for 48 hours of being analyzed. Material characterization of the deposits was conducted using XRPD Rietveld method of qualitative and quantitative mineralogical phase analysis. XRF was employed for bulk chemical elemental analysis of the scale obtained. The sample A using analytical grade powder provided the major phases of struvite-(K and struvite. In constrast, the major phase of newberyite and minor phases of lepidocrocite (FeOOH and niter (KNO3 was observed by following changes in the lowest purity of powder (Sample B. Analysis of the experimental data suggests a solution mediated transformation process as a possible mechanism of struvite transformation.

  13. Carbonate precipitates and bicarbonate secretion in the intestine of sea bass, Dicentrarchus labrax.

    Science.gov (United States)

    Faggio, Caterina; Torre, Agata; Lando, Gabriele; Sabatino, Giuseppe; Trischitta, Francesca

    2011-05-01

    The aim of this paper was to study the chemical composition of the precipitates found in the intestine of Dicentrarchus labrax and the source of HCO(3)(-) secreted into the intestinal lumen. The chemical analysis was performed by employing the potentiometric double titration method and by means of an electron microscope coupled with a spectrometer and X-ray powder diffraction. The results obtained suggest the presence of very insoluble intestinal precipitates, presumably formed by a mixture of CaCO(3) and MgCO(3), with a higher quantity of the former with respect to the latter. HCO(3)(-) secretion rate was investigated with the aid of the pH stat method in isolated tissues mounted in Ussing chamber, where the transepithelial electrical parameters were also measured. When the serosal surface of the intestinal mucosa was bathed in HCO(3)(-)-Ringer bubbled with 1% CO(2) in O(2) while the serosal surface was bathed in HCO(3)(-) free Ringer solution bubbled with pure O(2), bicarbonate secretion proceeded at an almost stable rate of 0.9 ± 0.05 μeq cm(-2) h(-1) for about 3 h while I(sc) maintained a constant value of 38 ± 1.5 μA cm(-2). The carbonic anhydrase inhibitor ethoxyzolamide elicited a progressive reduction of HCO(3)(-) secretion that was about 75% of the initial value after 80 min. When serosal HCO(3)(-)-CO(2) saline was substituted with Hepes-O(2) saline base secretion progressively declined reaching a value of about 20% of the initial value. It was also strongly inhibited when Na(+) was substituted with the impermeant cation choline and when either DIDS or ouabain were added to the basolateral side. These results suggest that most of the bicarbonate secreted is of extracellular source and is probably transported across the basolateral membrane by both Na(+) independent mechanism and Na(+) dependent transporter, presumably a NaHCO(3) cotransport. PMID:21152925

  14. Studies on the sublimation of tungsten single crystal (110) face and the influence of carbon

    International Nuclear Information System (INIS)

    Evaporation of tungsten single crystals face (110) is studied in ultrahigh vacuum (better than 1x10-9 torr) by Langmuir method. Small admixtures of carbon are shown to markedly influence the process. Carbon hinders the evaporation and increases the sublimation energy by 25 kcal. The data obtained show that the reported parametres of tungsten evaporation refer to a carbon-containing material

  15. Precipitation pulse dynamics of carbon sequestration and efflux in highly weatherable soils

    Science.gov (United States)

    Barron-Gafford, G.; Minor, R.; Van Haren, J. L.; Dontsova, K.; Troch, P. A.

    2013-12-01

    Soils are the primary pool for terrestrial carbon on Earth, and loss of that carbon to the atmosphere or hydrosphere represents a significant efflux that can impact a host of other downstream processes. Soil respiration (Rsoil), the efflux of CO2 to the atmosphere, represents the major pathway by which carbon is lost from the soil system in more weathered soils. However, in newly formed soils, chemical weathering can significantly deplete soil CO2 concentrations. As vegetation colonizes these soils, multiple interacting and contradictory pathways evolve such that soil CO2 concentrations increase in response to plant inputs but are decreased through chemical reactions. Furthermore, abiotic drivers of soil temperature and moisture likely differentially affect these processes. Understanding the bio-geo-chemical drivers and feedbacks associated with soil CO2 production and efflux in the critical zone necessitates an integrated science approach, drawing on input from plant physiologists, bio- and geochemists, and hydrologists. Here, we created a series of 1-meter deep mesocosms filled with granular basalt that supported either a woody mesquite shrub, a bunchgrass, or was left as bare soil. Use of multiple plant functional types allowed us to explore the impacts of plant structure (primarily rooting profiles) on critical zone function in terms of water and carbon exchange surrounding precipitation pulse dynamics. Each mesocosm was outfitted with an array of soil moisture, temperature, water potential, and CO2 concentration sensors at the near-surface, 30, 55, and 80cm depths to quantify patterns of soil moisture and respiratory CO2 efflux in response to rainfall events of varying magnitude and intervening periods of drought. Five replicates of each were maintained under current ambient or projected (+4oC) air temperatures. In addition, we used minirhizotrons to quantify the response of roots to episodic rainfall and confirm differences among plant types and collected

  16. Misorientation effect of grain boundary on the formation of discontinuous precipitation in second and third generation single crystal superalloys

    Directory of Open Access Journals (Sweden)

    Yu Zhengrong

    2014-01-01

    Full Text Available [001] tilt artificial grain boundaries of Ni-based single crystal superalloys CMSX-4 and DD10 have been prepared by self-diffusion bonding. The microstructural stability of 0 ∼ 30∘ artificial grain boundaries have been investigated after heat treatment at 1100 ∘C for 0 ∼ 300 h. TCP phases and cellular colony developed on boundaries are related to misorientation angle of the bonded boundaries of DD10 and DD10 alloys as well as the bonded boundaries of CMSX-4 and DD10 alloys. The heterogeneous nucleation of TCP phase, enveloped by γ′ film, occurred along 15∘ and 20∘ boundaries. Discontinuous Precipitation (DP reaction occurred along high misorientation angle (20∘∼ 30∘ boundaries. However, no TCP phase formation existed along grain boundaries with different misorientation angles in CMSX-4/CMSX-4 bonded alloys as well as for a 0∘ boundary in DD10/DD10 and CMSX-4/DD10 bonded alloys. The current study clearly suggests that grain boundary precipitation and its morphology were influenced by the misorientation angle of grain boundary and the content of refractory elements in alloy.

  17. Soil carbon dioxide emissions in response to precipitation frequency in the Loess Plateau, China

    Science.gov (United States)

    Precipitation events can induce episodic CO2 emissions, so called the “Birch Effect”, but how precipitation frequency influences the mechanisms responsible for this effect in dryland cropping systems is not well known. We evaluated the effect of three precipitation frequencies (5-, 10-, and 20-d int...

  18. The aging by precipitation of Nb (C,N) in extra low carbon content steel

    International Nuclear Information System (INIS)

    Carbonitride precipitation has been studied in a high-niobium acicular - ferrite - type steel. Interphase precipitation occurred only in those samples in which high transformation temperatures led to distinctly polygonal-ferrite microestructures. In this latter case, precipitation occurred during a subsequent aging treatment, with a strong tendency for heterogeneous nucleation on dislocations. (Author)

  19. Carbon Nanotube Liquid Crystals: Nematic Droplets and Coarsening Dynamics

    Science.gov (United States)

    Behabtu, Natnael; Senyuk, Bohdan; Smalyukh, Ivan; Pasquali, Matteo

    2012-02-01

    On a fundamental basis, carbon nanotubes (CNTs) offer a new model molecule to explore the dynamics and phases of rigid rods and test theories. Their large aspect ratio (100 to 100,000) and persistence length (˜ 100 microns) allow exploring the physics of nematic phases with high Frank elastic constant. Moreover, understanding of CNT liquid crystals is key to their rational processing into ordered materials such as fibers. Here we report the formation of elongated nematic droplets of CNTs in chlorosulfonic acid. In nematic droplets, a continuous transition from a homogeneous to bipolar nematic director field is expected theoretically, as a function of droplet volume; yet, experimental determination of such transition has been elusive. We show that CNT nematic droplets display such transition. We study the coarsening dynamics of positive and negative nematic droplets and observe that two or more droplets merge by matching their nematic director. Merging scenarios that lead to defect formation are not observed. Negative tactoids (isotropic phase in liquid crystalline continuum) merge through attractive forces induced by the nematic director distortion with quadrupolar symmetry.

  20. Study on the Functionality of Nano-Precipitated Calcium Carbonate as Filler in Thermoplastics

    Science.gov (United States)

    Basilia, Blessie A.; Panganiban, Marian Elaine G.; Collado, Archilles Allen V. C.; Pesigan, Michael Oliver D.; de Yro, Persia Ada

    This research aims to investigate the functionality of nano-precipitated calcium carbonate (NPCC) as filler in thermoplastic resins based on property enhancement. Three types of thermoplastics were used: polyethylene (PE), polypropylene (PP) and polyvinyl chloride (PVC). The resins were evaluated by determining the effect of different NPCC loading on the chemical structure, thermal and mechanical properties of thermoplastics. Results showed that there was an interfacial bonding with the NPCC surface and the thermoplastics. Change in absorption peak and area were predominant in the PVC filled composite. There was a decreased in crystallinity of the PE and PP with the addition of filler. Tremendous increase on the tensile and impact strength was exhibited by the NPCC filled PVC composites while PE and PP composites maintained a slight increase in their mechanical properties. Nano-sized filler was proven to improve the mechanical properties of thermoplastics compared with micron-sized filler because nano-sized filler has larger interfacial area between the filler and the polymer matrix.

  1. Thin graphite films formation by carbon precipitation in metals: diffusion approach

    Science.gov (United States)

    Shvets, Petr V.; Obraztsov, Alexander N.

    2016-03-01

    Thin graphite films attract significant interest due to their unique physical properties and potential applications. Chemical vapor deposition in the presence of metal catalysts is one of the most promising and widely used techniques to produce these films. There are many experimental works devoted to the material synthesis; however, the results are usually obtained by the trial-and-error method without a proper understanding of the processes behind the experiment. We theoretically analyze the carbon diffusion processes inside a metal substrate during the deposition. The theory allows interconnection of the deposition parameters with the thickness of produced graphite films. Numerically solving the diffusion equations for the real systems, we obtained a good correlation between simulations and experimental data. Based on our simulations, we made some conclusions about the formation of graphite films by the precipitation process. The numerical simulations were mostly done for the popular nickel substrates, but we also made some calculations for iron, showing that it also could be used to form thin graphite films under certain conditions.

  2. Carbon/Liquid Crystal Polymer Prepreg for Cryogenic and High-Temp Applications Project

    Data.gov (United States)

    National Aeronautics and Space Administration — KaZaK Composites proposes to develop a pultrusion process to produce carbon fiber / liquid crystal polymer (LCP) prepreg, a first for this category of materials and...

  3. Multiwall carbon nanotubes doped ferroelectric liquid crystal composites: A study of modified electrical behavior

    Energy Technology Data Exchange (ETDEWEB)

    Neeraj, E-mail: neerajvenus@gmail.com [Department of Physics, Sant Hira Dass Kanya Maha Vidyalaya, Kala Sanghian, Kapurthala 144623, Punjab (India); Raina, K.K., E-mail: kkraina@gmail.com [Materials Research Laboratory, School of Physics and Materials Science, Thapar University, Patiala 147004, Punjab (India)

    2014-02-01

    We systematically investigated the role of carbon nanotubes and their nature of interaction with the high polarization ferroelectric liquid crystal molecules that causes a change in the dynamic behavior of the liquid crystals. The carbon nanotubes were functionalized with carboxyl group (–COOH) before dispersion in order to enhance their stability in the liquid crystal medium. For the systematic investigation of a non linear behavior of dispersed composite systems, results for various physical properties were determined by thermal, morphological and dielectric studies in the planer aligned 5 μm thickness cells. An effort has also gone into detail to investigate these properties with varying concentration (0.02 wt%, 0.05 wt% and 0.1 wt%) of multiwall carbon nanotubes. The various carbon nanotubes doped ferroelectric liquid crystal thin film composites have shown enhanced dielectric strength and dielectric permittivity values as compared to the undoped sample.

  4. Crystallization and melting behavior of multi-walled carbon nanotube-reinforced nylon-6 composites

    NARCIS (Netherlands)

    Phang, In Yee; Ma, Jianhua; Shen, Lu; Liu, Tianxi; Zhang, Wei-De

    2006-01-01

    The crystallization and melting behavior of neat nylon-6 (PA6) and multi-walled carbon nanotubes (MWNTs)/PA6 composites prepared by simple melt-compounding was comparatively studied. Differential scanning calorimetry (DSC) results show two crystallization exotherms (TCC, 1 and TCC, 2) for PA6/MWNTs

  5. Pentagonal monolayer crystals of carbon, boron nitride, and silver azide

    Energy Technology Data Exchange (ETDEWEB)

    Yagmurcukardes, M., E-mail: mehmetyagmurcukardes@iyte.edu.tr; Senger, R. T., E-mail: tugrulsenger@iyte.edu.tr [Department of Physics, Izmir Institute of Technology, 35430 Urla, Izmir (Turkey); Sahin, H.; Kang, J.; Torun, E.; Peeters, F. M. [Department of Physics, University of Antwerp, Campus Groenenborgerlaan, 2020, Antwerp (Belgium)

    2015-09-14

    In this study, we present a theoretical investigation of structural, electronic, and mechanical properties of pentagonal monolayers of carbon (p-graphene), boron nitride (p-B{sub 2}N{sub 4} and p-B{sub 4}N{sub 2}), and silver azide (p-AgN{sub 3}) by performing state-of-the-art first principles calculations. Our total energy calculations suggest feasible formation of monolayer crystal structures composed entirely of pentagons. In addition, electronic band dispersion calculations indicate that while p-graphene and p-AgN{sub 3} are semiconductors with indirect bandgaps, p-BN structures display metallic behavior. We also investigate the mechanical properties (in-plane stiffness and the Poisson's ratio) of four different pentagonal structures under uniaxial strain. p-graphene is found to have the highest stiffness value and the corresponding Poisson's ratio is found to be negative. Similarly, p-B{sub 2}N{sub 4} and p-B{sub 4}N{sub 2} have negative Poisson's ratio values. On the other hand, the p-AgN{sub 3} has a large and positive Poisson's ratio. In dynamical stability tests based on calculated phonon spectra of these pentagonal monolayers, we find that only p-graphene and p-B{sub 2}N{sub 4} are stable, but p-AgN{sub 3} and p-B{sub 4}N{sub 2} are vulnerable against vibrational excitations.

  6. Growth of Large-Area Single- and Bi-Layer Graphene by Controlled Carbon Precipitation on Polycrystalline Ni Surfaces

    OpenAIRE

    Reina, Alfonso; Thiele, Stefan; Jia, Xiaoting; Bhaviripudi, Sreekar; Dresselhaus, Mildred S.; Schaefer, Juergen A.; Kong, Jing

    2009-01-01

    We report graphene films composed mostly of one or two layers of graphene grown by controlled carbon precipitation on the surface of polycrystalline Ni thin films during atmospheric chemical vapor deposition (CVD). Controlling both the methane concentration during CVD and the substrate cooling rate during graphene growth can significantly improve the thickness uniformity. As a result, one- or two- layer graphene regions occupy up to 87% of the film area. Single layer coverage accounts for 5%–...

  7. Warming rather than increased precipitation increases soil recalcitrant organic carbon in a semiarid grassland after 6 years of treatments.

    Directory of Open Access Journals (Sweden)

    Xiaoqi Zhou

    Full Text Available Improved understanding of changes in soil recalcitrant organic carbon (C in response to global warming is critical for predicting changes in soil organic C (SOC storage. Here, we took advantage of a long-term field experiment with increased temperature and precipitation to investigate the effects of warming, increased precipitation and their interactions on SOC fraction in a semiarid Inner Mongolian grassland of northern China since April 2005. We quantified labile SOC, recalcitrant SOC and stable SOC at 0-10 and 10-20 cm depths. Results showed that neither warming nor increased precipitation affected total SOC and stable SOC at either depth. Increased precipitation significantly increased labile SOC at the 0-10 cm depth. Warming decreased labile SOC (P = 0.038 and marginally but significantly increased recalcitrant SOC at the 10-20 cm depth (P = 0.082. In addition, there were significant interactive effects of warming and increased precipitation on labile SOC and recalcitrant SOC at the 0-10 cm depth (both P<0.05, indicating that that results from single factor experiments should be treated with caution because of multi-factor interactions. Given that the absolute increase of SOC in the recalcitrant SOC pool was much greater than the decrease in labile SOC, and that the mean residence time of recalcitrant SOC is much greater, our results suggest that soil C storage at 10-20 cm depth may increase with increasing temperature in this semiarid grassland.

  8. Effect of oxygen and carbon impurities on the performance of silicon single crystal solar cells

    International Nuclear Information System (INIS)

    BSF solar cells are fabricated using B-doped wafers cut from Czochralski Si(100) single crystals. The effect of unintentional impurities of Oxygen and Carbon atoms on the solar cell performance parameters have been studied. The presence of carbon atoms shows an improvement in all parameters particularly the short circuit current where as oxygen shows an adverse effect. (author). 13 refs, 1 fig

  9. Study on crystal transformation process of magnesium carbonate hydrate based on salt lake magnesium resource utilization

    OpenAIRE

    Du, Juan; Chen, Zhen; WU, Yu-Long; YANG, Ming-De

    2013-01-01

    The crystal transformation process of magnesium carbonate hydrate by the reaction of magnesium sulfate (MgSO4) with ammonium carbonate [(NH4)2CO3] was investigated. MgSO4 is one of the main magnesium resources of the Lop Nur salt lake in the Xinjiang Autonomous Region of China. Magnesium carbonate hydrates with different chemical compositions were prepared. The transformation process of the 2 crystals, MgSO4 and (NH4)2CO3, was analyzed by Raman spectroscopy, and the associated chang...

  10. Studies in sublimation of tungsten single crystal (110) face and the influence of carbon

    Energy Technology Data Exchange (ETDEWEB)

    Dekhtyar, I.Ya.; Kolesnik, V.M.; Patoka, V.I.; Silant' ev, V.I.

    1975-12-01

    Evaporation of the tungsten single crystal (110) face was studied in ultrahigh vacuum (better than 1.10/sup -9/ Torr) using the Langmuir method. The influence of carbon impurities on the evaporation parameters was found out and carbon is shown to increase the sublimation energy by 25 kcal. The data obtained show that the parameters of tungsten evaporation available in literature should be related to carbon-containing materials.

  11. Catalytic Oxidation of Propylene, Toluene, Carbon Monoxide, and Carbon Black over Au/CeO2 Solids: Comparing the Impregnation and the Deposition-Precipitation Methods

    Directory of Open Access Journals (Sweden)

    Antoine Aboukaïs

    2013-01-01

    Full Text Available Au/CeO2 solids were prepared by two methods: deposition-precipitation (DP and impregnation (Imp. The prepared solids were calcined under air at 400°C. Both types of catalysts have been tested in the total oxidation of propylene, toluene, carbon monoxide, and carbon black. Au/CeO2-DP solids were the most reactive owing to the high number of gold nanoparticles and Au+ species and the low concentration of Cl- ions present on its surface compared to those observed in Au/CeO2-Imp solids.

  12. Carbon and hydrogen isotope composition of plant biomarkers as proxies for precipitation changes across Heinrich Events in the subtropics

    Science.gov (United States)

    Arnold, T. E.; Freeman, K.; Brenner, M.; Diefendorf, A. F.

    2014-12-01

    Lake Tulane is a relatively deep (~23 m) solution lake in south-central Florida. Its depth and location on a structural high, the Lake Wales Ridge, enabled continuous lacustrine sediment accumulation over the past >60,000 years. Pollen in the lake sediments indicate repeated major shifts in the vegetation community, with six peaks in Pinus (pine) abundance that coincide with the most intense cold phases of Dansgaard-Oeschger cycles and the Heinrich events that terminate them. Alternating with Pinus peaks are zones with high relative percentages of Quercus (oak), Ambrosia (ragweed), Lyonia (staggerbush) and Ceratiola (rosemary) pollen, genera that today occupy the most xeric sites on the Florida landscape. This suggests the pollen record indicates the Pinus phases, and therefore Heinrich Events, were wetter than the intervening Quercus phases. To test the connection between Heinrich Events and precipitation in Florida, we analyzed the carbon (δ13C) and hydrogen (δD) isotope signatures of plant biomarkers extracted from the Lake Tulane sediment core as proxies of paleohydrology. The δ13C of plant biomarkers, such as n-alkanes and terpenoids, are determined, in part, by changes in water-use efficiency (WUE = Assimilation/Transpiration) in plant communities, which changes in response to shifts in mean annual precipitation. Plant δ13C values can, therefore, provide a rough indication of precipitation changes when other factors, such as plant community, are relatively stable throughout time. Paleohydrology is also recorded in the δD of plant leaf waxes, which are strongly controlled by precipitation δD. In this region, precipitation δD is negatively correlated with rainfall amount (i.e. the "amount" effect) and positively correlated with aridity. Thus, the δ13C and δD signatures of molecular plant biomarkers provide relative indicators of precipitation change, and when combined, provide a test of our hypothesis that vegetation changes in this region are driven

  13. The influence of solution stoichiometry on surface-controlled Ca isotope fractionation during Ca carbonate precipitation from Mono Lake, California

    Science.gov (United States)

    Nielsen, L. C.; Depaolo, D. J.

    2010-12-01

    Precipitation of calcite and aragonite from aqueous solution causes kinetic stable Ca isotope fractionation under conditions where Ca2+ is greatly in excess of CO32-. Research on carbonate mineral growth from low Ca2+:CO32- activity ratio solutions is lacking. Mono Lake, California is a highly alkaline lake with a Ca2+:CO32- activity ratio of 9.6 x 10-4, over five orders of magnitude lower than typical terrestrial fresh and ocean water. Aragonitic tufa towers grow along the lakeshore due to the mixing of lake water and Ca-rich spring water, while fine aragonite particles precipitate directly from the lake water, accumulating on the lake bottom. Variations in the Ca2+:CO32- activity ratio affect calcite growth kinetics and could affect the partitioning of Ca isotopes during carbonate precipitation. However, the relationship between solution stoichiometry, microscopic mineral growth mechanisms and calcium isotope fractionation is poorly understood. We analyzed the Sr and Ca isotopic compositions of a suite of lake water, spring, tufa and lake bottom sediment samples from the Mono Basin. Using the Sr isotope signatures of endmember water sources (pure lake water and shoreline spring water), we determined the compositions of carbonate mineral growth solutions, associated isotope separations (Δ44/40Cas-f = δ44/40Casolid - δ44/40Cafluid) and precipitation rates. While lake bottom aragonite precipitates directly from lake water (Ca2+:CO32- ≈ 10-3), tufa grows from mixed solutions with Ca2+:CO32- activity ratios approaching 10, so carbonate precipitation in Mono Lake spans a four order of magnitude range in solution stoichiometry. At Mono Lake, Δ44/40Cas-f and calculated precipitation rates vary between -0.6±0.15‰ at 1.5×10-9 mol m-2 s-1 for aragonite precipitating from lake water and ~ -1.0±0.15‰ at up to 4×10-8 mol m-2 s-1 for tufa growing from mixed spring and lake water. These values are consistent with fractionation observed during CaCO3 precipitation at

  14. Consolidation of degraded ornamental porous limestone stone by calcium carbonate precipitation induced by the microbiota inhabiting the stone.

    Science.gov (United States)

    Jimenez-Lopez, C; Rodriguez-Navarro, C; Piñar, G; Carrillo-Rosúa, F J; Rodriguez-Gallego, M; Gonzalez-Muñoz, M T

    2007-08-01

    Although it has already been shown that calcareous stone can be consolidated by using a bacterially inoculated culture medium, a more user-friendly method is the in situ application of a sterile culture medium that is able to activate, among the microbial community of the stone, those bacteria with a potential for calcium carbonate precipitation. In order to test this new method for stone consolidation, non-sterilized decayed porous limestone was immersed in sterile nutritional media. Results were compared to those of the runs in which stone sterilized prior to the treatment was used. The effects of the microbial community on stone consolidation were determined by recording the evolution of the culture media chemistry. The treated stone was tested for mechanical resistance and porosity. Results demonstrate that the tested media were able to activate bacteria from the microbial community of the stone. As a consequence of the growth of these bacteria, an alkalinization occurred that resulted in calcium carbonate precipitation. The new precipitate was compatible with the substrate and consolidated the stone without pore plugging. Therefore, a good candidate to in situ consolidate decayed porous limestone is the application of a sterile culture medium with the characteristics specified in the present study.

  15. The peculiar electrical response of liquid crystal-carbon nanotube systems as seen by impedance spectroscopy

    Science.gov (United States)

    García-García, A.; Vergaz, R.; Algorri, J. F.; Geday, M. A.; Otón, J. M.

    2015-09-01

    Conductive nanoparticles, especially elongated ones such as carbon nanotubes, dramatically modify the electrical behavior of liquid crystal cells. These nanoparticles are known to reorient with liquid crystals in electric fields, causing significant variations of conductivity at minute concentrations of tens or hundreds ppm. The above notwithstanding, impedance spectroscopy of doped cells in the frequency range customarily employed by liquid crystal devices, 100 Hz-10 kHz, shows a relatively simple resistor/capacitor response where the components of the cell can be univocally assigned to single components of the electrical equivalent circuit. However, widening the frequency range up to 1 MHz or beyond reveals a complex behavior that cannot be explained with the same simple EEC. Moreover, the system impedance varies with the application of electric fields, their effect remaining after removing the field. Carbon nanotubes are reoriented together with liquid crystal reorientation when applying voltage, but barely reoriented back upon liquid crystal relaxation once the voltage is removed. Results demonstrate a remarkable variation in the impedance of the dielectric blend formed by liquid crystal and carbon nanotubes, the irreversible orientation of the carbon nanotubes and possible permanent contacts between electrodes.

  16. The peculiar electrical response of liquid crystal-carbon nanotube systems as seen by impedance spectroscopy

    International Nuclear Information System (INIS)

    Conductive nanoparticles, especially elongated ones such as carbon nanotubes, dramatically modify the electrical behavior of liquid crystal cells. These nanoparticles are known to reorient with liquid crystals in electric fields, causing significant variations of conductivity at minute concentrations of tens or hundreds ppm. The above notwithstanding, impedance spectroscopy of doped cells in the frequency range customarily employed by liquid crystal devices, 100 Hz–10 kHz, shows a relatively simple resistor/capacitor response where the components of the cell can be univocally assigned to single components of the electrical equivalent circuit. However, widening the frequency range up to 1 MHz or beyond reveals a complex behavior that cannot be explained with the same simple EEC. Moreover, the system impedance varies with the application of electric fields, their effect remaining after removing the field. Carbon nanotubes are reoriented together with liquid crystal reorientation when applying voltage, but barely reoriented back upon liquid crystal relaxation once the voltage is removed. Results demonstrate a remarkable variation in the impedance of the dielectric blend formed by liquid crystal and carbon nanotubes, the irreversible orientation of the carbon nanotubes and possible permanent contacts between electrodes. (paper)

  17. Variation in the stable carbon and nitrogen isotope composition of plants and soil along a precipitation gradient in northern China.

    Directory of Open Access Journals (Sweden)

    Jian-Ying Ma

    Full Text Available Water availability is the most influential factor affecting plant carbon (δ(13C and nitrogen (δ(15N isotope composition in arid and semi-arid environments. However, there are potential differences among locations and/or species in the sensitivity of plant δ(13C and δ(15N to variation in precipitation, which are important for using stable isotope signatures to extract paleo-vegetation and paleo-climate information. We measured δ(13C and δ(15N of plant and soil organic matter (SOM samples collected from 64 locations across a precipitation gradient with an isotherm in northern China. δ(13C and δ(15N for both C(3 and C(4 plants decreased significantly with increasing mean annual precipitation (MAP. The sensitivity of δ(13C to MAP in C(3 plants (-0.6 ± 0.07‰/100 mm was twice as high as that in C(4 plants (-0.3 ± 0.08‰/100 mm. Species differences in the sensitivity of plant δ(13C and δ(15N to MAP were not observed among three main dominant plants. SOM became depleted in (13C with increasing MAP, while no significant correlations existed between δ(15N of SOM and MAP. We conclude that water availability is the primary environmental factor controlling the variability of plant δ(13C and δ(15N and soil δ(13C in the studied arid and semi-arid regions. Carbon isotope composition is useful for tracing environmental precipitation changes. Plant nitrogen isotope composition can reflect relative openness of ecosystem nitrogen cycling.

  18. The Origin of Magnetite Crystals in ALH84001 Carbonate Disks

    Science.gov (United States)

    Thomas-Keprta, K. L.; Clemett, S. J.; Wentworth, S. J.; McKay, D. S.; Gibson, E. K., Jr.

    2012-01-01

    Martian meteorite ALH84001 preserves evidence of interaction with aqueous fluids while on Mars in the form of microscopic carbonate disks believed to have formed approx 3.9 Ga ago at beginning of the Noachian epoch. Intimately associated within and throughout these carbonate disks are nanocrystal magnetites (Fe3O4) with unusual chemical and physical properties, whose origins have become the source of considerable debate. One group of hypotheses argues that these magnetites are the product of partial thermal decomposition of the host carbonate. Alternatively, the origins of magnetite and carbonate may be unrelated; that is, from the perspective of the carbonate the magnetite is allochthonous. We have sought to resolve between these hypotheses through the detailed characterized of the compositional and structural relationships between the carbonate disks, their associated magnetites and the orthopyroxene matrix in which they are embedded. Comparison of these results with experimental thermal decomposition studies of sideritic carbonates conducted under a range of heating scenarios suggests that the magnetite nanocrystals in the ALH84001 carbonate disks are not the products of thermal decomposition.

  19. Dehydration and crystallization of amorphous calcium carbonate in solution and in air.

    Science.gov (United States)

    Ihli, Johannes; Wong, Wai Ching; Noel, Elizabeth H; Kim, Yi-Yeoun; Kulak, Alexander N; Christenson, Hugo K; Duer, Melinda J; Meldrum, Fiona C

    2014-01-01

    The mechanisms by which amorphous intermediates transform into crystalline materials are poorly understood. Currently, attracting enormous interest is the crystallization of amorphous calcium carbonate, a key intermediary in synthetic, biological and environmental systems. Here we attempt to unify many contrasting and apparently contradictory studies by investigating this process in detail. We show that amorphous calcium carbonate can dehydrate before crystallizing, both in solution and in air, while thermal analyses and solid-state nuclear magnetic resonance measurements reveal that its water is present in distinct environments. Loss of the final water fraction--comprising less than 15% of the total--then triggers crystallization. The high activation energy of this step suggests that it occurs by partial dissolution/recrystallization, mediated by surface water, and the majority of the particle then crystallizes by a solid-state transformation. Such mechanisms are likely to be widespread in solid-state reactions and their characterization will facilitate greater control over these processes.

  20. ARTICLES: Orientation in Nematic Liquid Crystals Doped with Orange Dyes and Effect of Carbon Nanoparticles

    Science.gov (United States)

    Alicilar, Ahmet; Akkurt, Fatih; Kaya, Nihan

    2010-06-01

    Some properties of nematic liquid crystal E7 doped with two disperse orange dyes used together and effect of addition of carbon nanoparticles (single walled carbon nanotube or fullerene C60) on them were studied. Two dyes (disperse orange 11 and 13) having high solubility and order parameter were used as co-dopants. A notable increase in order parameter was obtained comparing to that of liquid crystal doped with single dye. When carbon nanoparticles were used as dopant, a decrease in order parameter was observed at low temperatures while it increased at high temperatures. When applied voltage changed, the order parameter abruptly increased in its threshold value and saturated in higher voltages as expected. An appreciable change in textures was not observed with addition of dopants. This addition gave rise to an increase in nematic-isotropic phase transition temperatures compared with that of pure liquid crystal.

  1. Thermodynamic analysis of carbide precipitates in a niobium-zirconium-carbon alloy

    Energy Technology Data Exchange (ETDEWEB)

    Farkas, D.M.; Groza, J.R.; Mukherjee, A.K. [Univ. of California, Davis, CA (United States). Dept. of Chemical Engineering and Materials Science

    1996-01-01

    Precipitation-strengthened niobium alloys have shown promise as high-temperature structural materials for aerospace applications. The achievement of suitable properties and superior creep resistance at service conditions requires that the second phase particles remain relatively small, stable, and evenly dispersed in the matrix. The key to this development lies in the thermodynamic evolution of the precipitate phase. This paper focuses on the thermodynamic driving force for formation of carbides in a precipitation-strengthened refractory metal alloy of niobium; Nb-1%Zr-0.1%C commercially known as PWC-11. An examination of the free energies of formation of the different carbide phases, their evolution and stability at the high temperatures, and a comparison with experimental analysis was made.

  2. Adsorption of crystal violet with diatomite earth&carbon by a modification of hydrothermal carbonization process.

    Science.gov (United States)

    Zhang, Yanzhuo; Li, Jun; Chen, Guanghui; Bian, Wei; Lu, Yun; Li, Wenjing; Zheng, Zhaoming; Cheng, Xiaojie

    2016-01-01

    The high colority and difficulty of decolorization are the most important tasks on printing and dyeing wastewater. This study investigates the ability of diatomite earth&carbon (DE&C) as an adsorbent to removal crystal violet (CV) from aqueous solutions. Fourier transform infrared spectroscopy results indicate the importance of functional groups during the adsorption of CV. The obtained N2 adsorption-desorption isotherm values accord with well IUPAC type II. Our calculations determined a surface area of 73.15 m(2) g(-1) for DE&C and an average pore diameter of 10.56 nm. Equilibrium data of the adsorption process fitted very well to the Langmuir model (R(2) > 0.99). The results of kinetics study showed that the pseudo-second-order model fitted to the experimental data well. The thermodynamic parameters were also evaluated. ΔH° 0 and ΔG° dye. Furthermore the positive value of ΔS° reflected good affinity of the CV dye. PMID:27003089

  3. Effect of pH and phosphate on calcium carbonate polymorphs precipitated at near-freezing temperature

    OpenAIRE

    Hu, Yu-Bin; Wolthers, Mariëtte; Wolf-Gladrow, Dieter A.; Nehrke, Gernot

    2015-01-01

    The effects of pH and phosphate on the precipitation of calcium carbonate polymorphs from aqueous solution were investigated. Experiments were carried out at near-freezing temperature and two different pH conditions (pH 13.4 and 9.0). At each pH condition, solutions having different concentrations of CaCl2 and NaHCO3 were mixed to achieve Ca/CO3 ratios of 1:1 and 10:1 at different pumping rates with and without phosphate. Results showed that, at pH 13.4, only ikaite wa...

  4. Carbon Isotopes in Pinus elliotti from Big Pine Key, Florida: Indicators of Seasonal Precipitation, ENSO and Disturbance Events

    Science.gov (United States)

    Rebenack, C.; Willoughby, H. E.; Anderson, W. T.; Cherubini, P.

    2013-12-01

    The South Florida coastal ecosystem is among the world's subtropical coastlines which are threatened by the potential effects of climate change. A well-developed localized paleohistory is essential in the understanding of the role climate variability/change has on both hydrological dynamics and disturbance event frequency and intensity; this understanding can then aid in the development of better predictive models. High resolution paleoclimate proxies, such as those developed from tree-ring archives, may be useful tools for extrapolating actual climate trends over time from the overlapping long-term and short-term climate cycles, such as the Atlantic Multidecadal Oscillation (AMO) and the El Niño-Southern Oscillation (ENSO). In South Florida, both the AMO and ENSO strongly influence seasonal precipitation, and a more complete grasp of how these cycles have affected the region in the past could be applied to future freshwater management practices. Dendrochronology records for the terrestrial subtropics, including South Florida, are sparse because seasonality for this region is precipitation driven; this is in contrast to the drastic temperature changes experienced in the temperate latitudes. Subtropical seasonality may lead to the complete lack of visible rings or to the formation of ring structures that may or may not represent annual growth. Fortunately, it has recently been demonstrated that Pinus elliottii trees in South Florida produce distinct annual growth rings; however ring width was not found to significantly correlate with either the AMO or ENSO. Dendrochronology studies may be taken a step beyond the physical tree-ring proxies by using the carbon isotope ratios to infer information about physiological controls and environmental factors that affect the distribution of isotopes within the plant. It has been well established that the stable isotope composition of cellulose can be related to precipitation, drought, large-scale ocean/atmospheric oscillations

  5. Effects of cosolvent on formation and morphology of microspheres in precipitation polymerization of divinylbenzene in supercritical carbon dioxide

    Institute of Scientific and Technical Information of China (English)

    Chun Sheng Li; Jing Cui Liang; Xiao Li Zhu; Xiang Zheng Kong

    2011-01-01

    Precipitation polymerizations of divinylbenzene (DVB) in pure supercritical carbon dioxide, and parallel runs with presence of a cosolvent were carried out. The results showed that use of acetone as the cosolvent contributed greatly to the formation of the monodisperse microspheres. PDVB microspheres, with obviously higher uniformity than reported up to date, were achieved using 6-7 mL of acetone in a reactor of 50 mL with DVB concentration of 0.4 mol/L under 16 MPa, a much lower pressure than previously reported without use of cosolvent.

  6. Microbial decomposition of dead grassland roots and its influence on the carbon cycle under changing precipitation patterns

    Science.gov (United States)

    Becerra, C.; Schimel, J.

    2013-12-01

    Soil is the largest reservoir of organic carbon in terrestrial ecosystems and as such, represents a potential sink for carbon dioxide.The decomposition products of dead roots buried in the soil is a contributor to soil organic carbon. However, changing precipitation patterns may affect its fate by influencing the microbial community responsible for decomposing dead roots. To assess the impact of changing precipitation patterns, we constructed microcosms with grassland soil collected from the UCSB Sedgwick Reserve, an active and long-term research site, and dead roots from greenhouse-grown grass, Bromus diandrus. Microcosms were wetted continuously, every seven days, or every twenty days. Sets of microcosms were periodically deconstructed to assess the soil versus the roots-associated microbial community and its function. Differences in respiration rates of microcosms continuously wetted or wetted every 7 days versus microcosms wetted every 20 days existed for the first 70 days. After which, no differences in respiration rates were seen with microcosms containing roots and the no roots control. Relatedly, after a 70% roots mass loss by day 50, there was no difference in the respiration rate of microcosms containing roots and the no roots control. More than half of the roots mass loss had occurred by 30 days. By the end of the incubation period, the roots mass loss in continuously wet and 7-day wetted microcosms were over 80% compared to 67% for the microcosms wetted every 20 days. Microbial biomass in the soil were constant over time and showed no difference in treatment except with the no roots control during the first half of the incubation period. Hydrolytic enzyme activities (β-1,4-glucosidase; α-1,4-glucosidase; β-1,4-xylosidase; β-1,4-cellobiosidase) on the roots versus the soil attached to the roots were over an order greater and decreased faster with the exception of N-acetyl-glucosaminidase and acid phosphatase. Oxidative enzyme activities (phenol

  7. Synthesis of high-purity precipitated calcium carbonate during the process of recovery of elemental sulphur from gypsum waste.

    Science.gov (United States)

    de Beer, M; Doucet, F J; Maree, J P; Liebenberg, L

    2015-12-01

    We recently showed that the production of elemental sulphur and calcium carbonate (CaCO3) from gypsum waste by thermally reducing the waste into calcium sulphide (CaS) followed by its direct aqueous carbonation yielded low-grade carbonate products (i.e. production of high-grade CaCO3 (i.e. >99 mass% as CaCO3) or precipitated calcium carbonate (PCC). The process used an acid gas (H2S) to improve the aqueous dissolution of CaS, which is otherwise poorly soluble. The carbonate product was primarily calcite (99.5%) with traces of quartz (0.5%). Calcite was the only CaCO3 polymorph obtained; no vaterite or aragonite was detected. The product was made up of micron-size particles, which were further characterised by XRD, TGA, SEM, BET and true density. Results showed that about 0.37 ton of high-grade PCC can be produced from 1.0 ton of gypsum waste, and generates about 0.19 ton of residue, a reduction of 80% from original waste gypsum mass to mass of residue that needs to be discarded off. The use of gypsum waste as primary material in replacement of mined limestone for the production of PPC could alleviate waste disposal problems, along with converting significant volumes of waste materials into marketable commodities. PMID:26316100

  8. Study of the effect of nano-sized precipitates on the mechanical properties of boron-added low-carbon steels by neutron scattering techniques.

    Science.gov (United States)

    Seong, B S; Cho, Y R; Shin, E J; Kim, S I; Choi, S-H; Kim, H R; Kim, Y J

    2008-10-01

    Small-angle neutron scattering (SANS) and neutron powder diffraction (ND) techniques were used to study quantitatively the effect of nano-sized precipitates and boron addition on the mechanical properties of low-carbon steels. SANS was used to evaluate nano-sized precipitates, smaller than about 600 A in diameter, and ND was used to determine the weight fraction of the cementite precipitates. Fine core-shell structured spherical precipitates with an average radius of ~50 A, such as MnS and/or CuS, surrounded by BN layers were observed in the boron-added (BA) low-carbon steels; fine spherical precipitates with an average radius of ~48 A were mainly observed in the boron-free (BF) low-carbon steels. In the BA steels, the number of boron precipitates, such as BN, Fe(3)(C,B) and MnS, surrounded by BN layers increased drastically at higher hot-rolling temperatures. The volume fraction of the fine precipitates of the BA steels was higher than that of the BF steels; this difference is related to the rapid growth of the BN layers on the MnS and CuS precipitates. Boron addition to low-carbon steels resulted in a reduction in strength and an improvement in elongation; this behaviour is related to the reduction of the solute carbon and the nitrogen contents in the ferrite matrix caused by the precipitation of BN, as well by the increase in the volume fraction of the cementites. PMID:19461851

  9. Reorientation of single-wall carbon nanotubes in negative anisotropy liquid crystals by an electric field.

    Science.gov (United States)

    García-García, Amanda; Vergaz, Ricardo; Algorri, José F; Zito, Gianluigi; Cacace, Teresa; Marino, Antigone; Otón, José M; Geday, Morten A

    2016-01-01

    Single-wall carbon nanotubes (SWCNT) are anisotropic nanoparticles that can cause modifications in the electrical and electro-optical properties of liquid crystals. The control of the SWCNT concentration, distribution and reorientation in such self-organized fluids allows for the possibility of tuning the liquid crystal properties. The alignment and reorientation of CNTs are studied in a system where the liquid crystal orientation effect has been isolated. Complementary studies including Raman spectroscopy, microscopic inspection and impedance studies were carried out. The results reveal an ordered reorientation of the CNTs induced by an electric field, which does not alter the orientation of the liquid crystal molecules. Moreover, impedance spectroscopy suggests a nonnegligible anchoring force between the CNTs and the liquid crystal molecules. PMID:27547599

  10. Reorientation of single-wall carbon nanotubes in negative anisotropy liquid crystals by an electric field

    Science.gov (United States)

    García-García, Amanda; Vergaz, Ricardo; Algorri, José F; Zito, Gianluigi; Cacace, Teresa; Marino, Antigone; Otón, José M

    2016-01-01

    Summary Single-wall carbon nanotubes (SWCNT) are anisotropic nanoparticles that can cause modifications in the electrical and electro-optical properties of liquid crystals. The control of the SWCNT concentration, distribution and reorientation in such self-organized fluids allows for the possibility of tuning the liquid crystal properties. The alignment and reorientation of CNTs are studied in a system where the liquid crystal orientation effect has been isolated. Complementary studies including Raman spectroscopy, microscopic inspection and impedance studies were carried out. The results reveal an ordered reorientation of the CNTs induced by an electric field, which does not alter the orientation of the liquid crystal molecules. Moreover, impedance spectroscopy suggests a nonnegligible anchoring force between the CNTs and the liquid crystal molecules. PMID:27547599

  11. Preparation and Crystallization of Carbon Nanotube/maleic Anhydride-grafted Polypropylene Composites

    Institute of Scientific and Technical Information of China (English)

    Xiaohua CHEN; Jing HU; Lingping ZHOU; Wenhua LI; Zi YANG; Yanguo WANG

    2008-01-01

    Carbon nanotube (CNT)/maleic acid anhydride (MAH)-grafted polypropylene (PP) composites were prepared by in situ grafting method. Infrared spectroscopy showed that the CNTs were linked to PP by MAH grafting. The microstructures and calorimetry analysis indicated that the crystallization behaviors of the filled and unfilled PP were quite different. The addition of CNTs dramatically reduced the spherulite size, increased crystallization rate and improved the thermal stability of PP. These results confirmed the expected nucleant effect of CNT on the crystallization of PP. Scanning and transmission electron microscopy showed that the CNTs were dispersed homogeneously, indicating that the original CNT bundles were separated into individual tubes by the grafting.

  12. A Layout for the Carbon Capture with Aqueous Ammonia without Salt Precipitation

    DEFF Research Database (Denmark)

    Bonalumi, Davide; Valenti, Gianluca; Lillia, Stefano;

    2016-01-01

    Super Critical power plant. Two layouts are simulated with Aspen Plus employing the recently recalibrated Extended UNIQUAC thermodynamic model. The first one operates at chilling conditions, which yield to salt precipitation, and is taken as reference because already analyzed in previous studies...

  13. Crystallization and self-assembly of flowerlike superstructures of calcium carbonate regulated by pepsin Langmuir monolayers

    International Nuclear Information System (INIS)

    Flowerlike superstructures of calcium carbonate were synthesized at air–water interface in the presence of pepsin Langmuir monolayers as the biomimetic template. The phase structure, morphology, and microstructure of the products obtained at various crystallization stages were characterized by means of X-ray diffraction, scanning electron microscopy, transmission electron microscopy, selected area electron diffraction and high resolution transmission electron microscopy. The structural and morphological evolution processes of the products from monodispersed nanoparticles to nanoparticle aggregates and flowerlike superstructures were investigated. Results indicate that the flowerlike superstructures of calcium carbonate are assembled from amorphous calcium carbonate nanoparticles. The growth and assembly of calcium carbonate minerals are significantly regulated by the pepsin Langmuir monolayers. Namely, the pepsin Langmuir monolayers stabilize amorphous calcium carbonate nanoparticles and direct their transformation to amorphous aggregates via non-oriented aggregation. The present approach presents a feasible way to manipulate the growth of inorganic crystal, which, hopefully, is to help better reveal the role of proteins in mineralization process and understand the mechanism of biomineralization. -- Highlights: ► Pepsin Langmuir monolayer as biomimetic template. ► Flower-like calcite crystals experience a novel assembly and growth process. ► The morphologic evolution and phase transformation were observed. ► The trace of initial nucleation site of CaCO3 at the interface was observed. ► The template directs the crystallization and growth process.

  14. Crystallization and self-assembly of flowerlike superstructures of calcium carbonate regulated by pepsin Langmuir monolayers

    Energy Technology Data Exchange (ETDEWEB)

    Xue, Zhonghui [Key Laboratory for Special Functional Materials of Ministry of Education, Henan University, Kaifeng 475004 (China); School of Physics and Chemistry, Henan Polytechnic University, Jiaozuo 454000 (China); Hu, Binbin; Dai, Shuxi [Key Laboratory for Special Functional Materials of Ministry of Education, Henan University, Kaifeng 475004 (China); Du, Zuliang, E-mail: zld@henu.edu.cn [Key Laboratory for Special Functional Materials of Ministry of Education, Henan University, Kaifeng 475004 (China)

    2012-10-15

    Flowerlike superstructures of calcium carbonate were synthesized at air-water interface in the presence of pepsin Langmuir monolayers as the biomimetic template. The phase structure, morphology, and microstructure of the products obtained at various crystallization stages were characterized by means of X-ray diffraction, scanning electron microscopy, transmission electron microscopy, selected area electron diffraction and high resolution transmission electron microscopy. The structural and morphological evolution processes of the products from monodispersed nanoparticles to nanoparticle aggregates and flowerlike superstructures were investigated. Results indicate that the flowerlike superstructures of calcium carbonate are assembled from amorphous calcium carbonate nanoparticles. The growth and assembly of calcium carbonate minerals are significantly regulated by the pepsin Langmuir monolayers. Namely, the pepsin Langmuir monolayers stabilize amorphous calcium carbonate nanoparticles and direct their transformation to amorphous aggregates via non-oriented aggregation. The present approach presents a feasible way to manipulate the growth of inorganic crystal, which, hopefully, is to help better reveal the role of proteins in mineralization process and understand the mechanism of biomineralization. -- Highlights: Black-Right-Pointing-Pointer Pepsin Langmuir monolayer as biomimetic template. Black-Right-Pointing-Pointer Flower-like calcite crystals experience a novel assembly and growth process. Black-Right-Pointing-Pointer The morphologic evolution and phase transformation were observed. Black-Right-Pointing-Pointer The trace of initial nucleation site of CaCO{sub 3} at the interface was observed. Black-Right-Pointing-Pointer The template directs the crystallization and growth process.

  15. Coprecipitation of (14)C and Sr with carbonate precipitates: The importance of reaction kinetics and recrystallization pathways.

    Science.gov (United States)

    Hodkin, David J; Stewart, Douglas I; Graham, James T; Burke, Ian T

    2016-08-15

    This study investigated the simultaneous removal of Sr(2+) and (14)CO3(2-) from pH>12 Ca(OH)2 solution by the precipitation of calcium carbonate. Initial Ca(2+):CO3(2-) ratios ranged from 10:1 to 10:100 (mM:mM). Maximum removal of (14)C and Sr(2+) both occurred in the system containing 10mM Ca(2+) and 1mM CO3(2-) (99.7% and 98.6% removal respectively). A kinetic model is provided that describes (14)C and Sr removal in terms of mineral dissolution and precipitation reactions. The removal of (14)C was achieved during the depletion of the initial TIC in solution, and was subsequently significantly affected by recrystallization of the calcite precipitate from an elongate to isotropic morphology. This liberated >46% of the (14)C back to solution. Sr(2+) removal occurred as Ca(2+) became depleted in solution and was not significantly affected by the recrystallization process. The proposed reaction could form the basis for low cost remediation scheme for (90)Sr and (14)C in radioactively contaminated waters (<$0.25 reagent cost per m(3) treated).

  16. Crystal structure of Brinzolamide: a carbonic anhydrase inhibitor.

    Science.gov (United States)

    Zheng, Huirong; Lou, Benyong

    2016-05-01

    In crystal structure of the title compound, C12H21N3O5S3 [systematic name: (R)-4-ethyl-amino-2-(3-meth-oxy-prop-yl)-3,4-di-hydro-2H-thieno[3,2-e][1,2]thia-zine-6-sulfonamide 1,1-dioxide], there exist three kinds of hydrogen-bonding inter-actions. The sulfonamide group is involved in hydrogen bonding with the secondary amine and the meth-oxy O atom, resulting in the formation of layers parallel to the bc plane. The layers are linked by an N-H⋯O hydrogen bond involving a sulfonamide O atom as acceptor and the secondary amine H atom as donor, which gives rise to the formation of a unique bilayer structure. The absolute structure of the mol-ecule in the crystal was determined by resonant scattering [Flack parameter = 0.01 (4)]. PMID:27308020

  17. Crystal structure of Brinzolamide: a carbonic anhydrase inhibitor

    Directory of Open Access Journals (Sweden)

    Huirong Zheng

    2016-05-01

    Full Text Available In crystal structure of the title compound, C12H21N3O5S3 [systematic name: (R-4-ethylamino-2-(3-methoxypropyl-3,4-dihydro-2H-thieno[3,2-e][1,2]thiazine-6-sulfonamide 1,1-dioxide], there exist three kinds of hydrogen-bonding interactions. The sulfonamide group is involved in hydrogen bonding with the secondary amine and the methoxy O atom, resulting in the formation of layers parallel to the bc plane. The layers are linked by an N—H...O hydrogen bond involving a sulfonamide O atom as acceptor and the secondary amine H atom as donor, which gives rise to the formation of a unique bilayer structure. The absolute structure of the molecule in the crystal was determined by resonant scattering [Flack parameter = 0.01 (4].

  18. Low Carbon Low Alloy Submicro-Steel with Nano-Precipitates

    Institute of Scientific and Technical Information of China (English)

    SongHongwei; ShiBi; ZhangJunbao; WangXiufang

    2005-01-01

    A submicro-steel sheet was successfully fabricated by severe warm-wiling at 773 K through a single pass. The microstructure was characterized first and the thermal stability of the submicro-steel was investigated by annealing the steel at different temperatures.Results indicate that grains are nearly equiaxial with an average diameter of 300 nm for grains near to the surface and 600 nm for grains at the center of the sheet and the submicro-steel can be subjected to annealing at 773 K without obvious grain growth. The formation of the submicro-structure can be related to a severe plastic deformation-induced grain refinement mechanism. The unusually high thermal stability can be attributed to the pinning effect of numerous uniformly-distributed nano-precipitates in the steel. The average diameter of the larger precipitates is about 30 nm and the smaller less than 10 inn.

  19. The sensitivity of tropical convective precipitation to the direct radiative forcings of black carbon aerosols emitted from major regions

    Directory of Open Access Journals (Sweden)

    C. Wang

    2009-10-01

    Full Text Available Previous works have suggested that the direct radiative forcing (DRF of black carbon (BC aerosols are able to force a significant change in tropical convective precipitation ranging from the Pacific and Indian Ocean to the Atlantic Ocean. In this in-depth analysis, the sensitivity of this modeled effect of BC on tropical convective precipitation to the emissions of BC from 5 major regions of the world has been examined. In a zonal mean base, the effect of BC on tropical convective precipitation is a result of a displacement of ITCZ toward the forcing (warming hemisphere. However, a substantial difference exists in this effect associated with BC over different continents. The BC effect on convective precipitation over the tropical Pacific Ocean is found to be most sensitive to the emissions from Central and North America due to a persistent presence of BC aerosols from these two regions in the lowermost troposphere over the Eastern Pacific. The BC effect over the tropical Indian and Atlantic Ocean is most sensitive to the emissions from South as well as East Asia and Africa, respectively. Interestingly, the summation of these individual effects associated with emissions from various regions mostly exceeds their actual combined effect as shown in the model run driven by the global BC emissions, so that they must offset each other in certain locations and a nonlinearity of this type of effect is thus defined. It is known that anthropogenic aerosols contain many scattering-dominant constituents that might exert an effect opposite to that of absorbing BC. The combined aerosol forcing is thus likely differing from the BC-only one. Nevertheless, this study along with others of its kind that isolates the DRF of BC from other forcings provides an insight of the potentially important climate response to anthropogenic forcings particularly related to the unique particulate solar absorption.

  20. Enzyme-accelerated and structure-guided crystallization of calcium carbonate: role of the carbonic anhydrase in the homologous system.

    Science.gov (United States)

    Müller, Werner E G; Schlossmacher, Ute; Schröder, Heinz C; Lieberwirth, Ingo; Glasser, Gunnar; Korzhev, Michael; Neufurth, Meik; Wang, Xiaohong

    2014-01-01

    The calcareous spicules from sponges, e.g. from Sycon raphanus, are composed of almost pure calcium carbonate. In order to elucidate the formation of those structural skeletal elements, the function of the enzyme carbonic anhydrase (CA), isolated from this species, during the in vitro calcium carbonate-based spicule formation, was investigated. It is shown that the recombinant sponge CA substantially accelerates calcium carbonate formation in the in vitro diffusion assay. A stoichiometric calculation revealed that the turnover rate of the sponge CA during the calcification process amounts to 25 CO2s(-1) × molecule CA(-1). During this enzymatically driven process, initially pat-like particles are formed that are subsequently transformed to rhomboid/rhombohedroid crystals with a dimension of ~50 μm. The CA-catalyzed particles are smaller than those which are formed in the absence of the enzyme. The Martens hardness of the particles formed is ~4 GPa, a value which had been determined for other biogenic calcites. This conclusion is corroborated by energy-dispersive X-ray spectroscopy, which revealed that the particles synthesized are composed predominantly of the elements calcium, oxygen and carbon. Surprising was the finding, obtained by light and scanning electron microscopy, that the newly formed calcitic crystals associate with the calcareous spicules from S. raphanus in a highly ordered manner; the calcitic crystals almost perfectly arrange in an array orientation along the two opposing planes of the spicules, leaving the other two plane arrays uncovered. It is concluded that the CA is a key enzyme controlling the calcium carbonate biomineralization process, which directs the newly formed particles to existing calcareous spicular structures. It is expected that with the given tools new bioinspired materials can be fabricated. PMID:23978410

  1. Precipitation and dissolution of calcium carbonate: key processes bridging the bio- and geosciences (Vladimir Ivanovich Vernadsky Medal Lecture)

    Science.gov (United States)

    Gattuso, J.-P.

    2012-04-01

    In this Vladimir Ivanovich Vernadsky medal lecture, I will focus on the biogeochemical cycle of calcium carbonate (CaCO3) which is arguably one of the best example of a set processes that bridge the bio- and geosciences. The main reactions involved are calcification and dissolution that, respectively, manufacture and destroy calcium carbonate. Biology is intimately involved in these two processes which are key controls of the Earth's climate and leave remains that are of great use to human societies (as building materials) and geoscientists. I will illustrate the bridge between the bio- and geosciences by providing brief examples for each of the following four issues. (1) The marine cycle of CaCO3 and its relationship with climate. The release of CO2 by the precipitation of calcium carbonate and the uptake of CO2 by its dissolution are important controls of atmospheric CO2 and climate. The vertical distribution of Ψ, the ratio of CO2 released/used per CaCO3 precipitated/dissolved in the ocean will be shown to be consistent with the Högbom-Urey reactions. (2) The use of CaCO3 in paleooceanography. The remains of calcium carbonate shells and skeletons are wonderful archives of past environmental changes. Their isotopic composition and the concen-tration of trace elements are invaluable in the reconstruction of past climate. I will address the challenge of calibrating one of the proxies used to reconstruct past ocean pH. (3) The challenge of understanding calcification. Despite having been investigated for decades, many aspects of the physiological and molecular processes involved in calcification by marine organisms remain obscure. Recent breakthroughs, mostly on reef-building corals, will be briefly reviewed. (4) The response of calcification and dissolution to environmental change. The critical importance of CaCO3 precipitation and dissolution as climate controls makes it vital to understand their response to global environmental changes such as ocean warming and

  2. Citrate effects on amorphous calcium carbonate (ACC) structure, stability, and crystallization

    DEFF Research Database (Denmark)

    Tobler, Dominique Jeanette; Rodriguez Blanco, Juan Diego; Dideriksen, Knud;

    2015-01-01

    Understanding the role of citrate in the crystallization kinetics of amorphous calcium carbonate (ACC) is essential to explain the formation mechanisms, stabilities, surface properties, and morphologies of CaCO3 biominerals. It also contributes to deeper insight into fluid-mineral inte...

  3. Thermally induced crystallization and phase evolution in powders derived from amorphous calcium phosphate precipitates with a Ca/P ratio of 1:1

    Science.gov (United States)

    Zyman, Zoltan; Epple, Matthias; Goncharenko, Anton; Rokhmistrov, Dmytro; Prymak, Oleg; Loza, Kateryna

    2016-09-01

    Calcium phosphate powders of calcium pyrophosphate α1-CPP (the metastable phase of the high-temperature polymorph α-CPP) and the polymorph β-CPP (stable in this range), of α1-CPP, β-CPP, α1-TCP (metastable polymorph of the high-temperature phase α-tricalcium phosphate) and β-tricalcium phosphate β-TCP were prepared by heating amorphous calcium phosphate (ACP) precipitates with the nominal Ca/P ratio of 1:1 by nitrate synthesis. α1-CPP/β-CPP resulted from a crystallization at 530-640 °C and subsequent heating to 980 °C of unwashed and lyophilized ACP. α1-CPP/β-CPP/α1-TCP/β-TCP was formed by crystallization at 620-720 °C, followed by heating of six-time washed and lyophilized ACP precipitates from an ultra-short synthesis. The activation energy for the crystallization of ACP to α1-CPP was determined with 165 kJ mol-1. The reason for the occurrence of the TCP phases (Ca/P ratio=1.5) from ACP (Ca/P ratio=1) is discussed. The powders are prospective biomaterials for bone substitution because they combine effective bioactive phases with the metastable polymorphs α1-CPP and α1-TCP.

  4. Influence of surface treatment of carbon fibers on electrochemical crystallization of calcium phosphate

    Institute of Scientific and Technical Information of China (English)

    TAO Ke; HUANG Su-ping; ZHOU Ke-chao

    2005-01-01

    Electrodeposition technique was used to coat calcium phosphate on carbon fiber which can be used to reinforce hydroxyapatite. The differences between fibers treated with and without nitric acid in electrodeposition were evaluated. The X-ray diffractometry results show that CaHPO4·2H2O is obtained as the kind of calcium phosphate coating on carbon fiber. The scanning electron microscopy photographs and deposit kinetic curve indicate that the influences of the functional group attained by nitric acid treatment, the crystal morphology and crystallization of the coating layers on the fiber with and without treatment rate are obviously different. The functional group, especially the acidic group, can act as nucleation centers of electrochemical crystallization.

  5. Effects of Strain-Induced Crystallization on Mechanical Properties of Elastomeric Composites Containing Carbon Nanotubes and Carbon Black

    International Nuclear Information System (INIS)

    The effects of strain-induced crystallization (SIC) on the mechanical properties of elastomeric composites as functions of extension ratio (λ), multi walled carbon nanotube (CNT) content, and carbon black (CB) content are investigated. The differential scanning calorimetry (DSC) analysis shows that the degree of crystallinity increases with the increase in the CB and CNT content. As λ increases, the glass transition temperature (Tg) of the composites increases, and the latent heat of crystallization (LHc) of the composites is maximum at λ=1.5. It is found that the mechanical properties have a linear relation with LHc, depending on the CNT content. According to the TGA (thermogravimetric analysis), the weight loss of the composite matrix is 94.3% and the weight of the composites decreases with the filler content. The ratio of tensile modulus (Ecomp/ Ematrix) is higher than that of tensile strength (σcomp/ σmatrix) because of the CNT orientation inside the elastomeric composites

  6. Testing the limits of the diffusion-production-equilibrium model of soil CO2: The effect of rapid carbonate precipitation on the pedogenic carbonate proxy

    Science.gov (United States)

    Wynn, J. G.; Chelladurai, J. L.

    2009-12-01

    A large body of terrestrial paleoenvironmental proxy research hinges on the well-established diffusion-production-equilibrium model of soil CO2. Although soil CO2 is the linchpin between the isotopic composition of pedogenic carbonate and the terrestrial biomass, it is not preserved directly in paleosols, and the model makes important boundary condition assumptions on processes that control its isotopic composition. The standard model assumes two-end member diffusional mixing between soil-respired CO2 and atmospheric CO2, and equilibrium precipitation of soil CaCO3 in an open system. We modified the boundary conditions of the standard model to specifically account for the flux and stable isotope fractionation of CO2 into the CaCO3 reservoir under partially closed-system conditions. Model calculations show that diversion of a relatively small fraction of the CO2 flux into CaCO3 results in a large change in the isotopic composition of soil CO2 and hence of CaCO3 at the sites of pedogenic carbonate accumulation. We also incubated two types of biomass (derived from C3 and C4 photosynthesis) in synthetic profiles with controlled conditions designed to test this modified model hypothesis. While soil CO2 from the surface horizons validated two-end member mixing, the δ13C values of CO2 from developing carbonate horizons was consistently 13C-depleted by several per mil compared to model predictions. This negative offset from the standard model mixing diagram (a Keeling Plot) is only consistent with the positive fractionation factor for carbonate precipitation in partially-closed system conditions. We also consider the conditions under which terrestrial paleoenvironmental proxy studies may be compromised by inappropriate boundary condition assumptions, in an effort to provide more robust model validation and application to terrestrial proxy data.

  7. Carbon-specific analysis of humic-like substances in atmospheric aerosol and precipitation samples.

    Science.gov (United States)

    Limbeck, Andreas; Handler, Markus; Neuberger, Bernhard; Klatzer, Barbara; Puxbaum, Hans

    2005-11-15

    A new approach for the carbon-specific determination of humic-like substances (HULIS) in atmospheric aerosols is presented. The method is based on a two-step isolation procedure of HULIS and the determination of HULIS carbon with a dissolved organic carbon analyzer. In the first step, a C18 solid-phase extraction is performed to separate HULIS from inorganic and hydrophilic organic sample constituents in aqueous sample solutions. The second isolation step is conducted on a strong anion exchanger to separate HULIS from remaining carbonaceous compounds. This ion chromatographic separation step including the subsequent on-line detection of HULIS carbon was performed fully automated to avoid the risk of sample contamination and to enhance the reproducibility of the method. With a 5-mL sample volume, a limit of detection of 1.0 mg C/L was obtained; this corresponds to an absolute amount of 5 microg of HULIS carbon. The reproducibility of the method given as the relative standard deviation was 4.3% (n = 10). The method was applied for the determination of water-soluble HULIS in airborne particulate matter. PM10 concentrations at an urban site in Vienna, Austria, ranged from around 0.1 to 1.8 microg of C/m(3) (n = 49); the fraction of water-soluble HULIS in OC was 12.1 +/- 7.2% (n = 49).

  8. Dissolved organic carbon and nitrogen in precipitation, throughfall and stemflow from Schima superba and Cunninghamia lanceolata plantations in subtropical China

    Institute of Scientific and Technical Information of China (English)

    GUO Jian-fen; YANG Yu-sheng; CHEN Guang-shui; LIN Peng

    2005-01-01

    Despite growing attention to the role of dissolved organic carbon (DOC) and dissolved organic nitrogen (DON) in forest nutrient cycling, their monthly concentration dynamics in forest ecosystems, especially in subtropical forests only were little known. The goal of this study is to measure the concentrations and monthly dynamics of DOC and DON in precipitation, throughfall and stemflow for two plantations of Schima superba (SS) and Chinese fir (Cunninghamia lanceolata, CF) in Jianou, Fujian, China. Samples of precipitation, throughfall and stemflow were collected on a rain event base from January 2002 to December 2002. Upon collection, all water samples were analyzed for DOC, NO3--N, NH4+-N and total dissolved N (TDN). DON was calculated by subtracting NO3--N and NH4+-N from TDN. The results showed that the precipitation had a mean DOC concentration of 1.7 mg·L-1 and DON concentration of 0.13 mg·L-1. The mean DOC and DON concentrations in throughfall were 11.2 and 0.24 mg·L-1 in the SS and 10.3 and 0.19 mg·L-1 in the CF respectively. Stemflow DOC and DON concentrations in the CF (19.1 and 0.66 mg·L-1 respectively) were significantly higher than those in the SS (17.6 and 0.48 mg·L-1 respectively). No clear monthly variation in precipitation DOC concentration was found in our study, while DON concentration in precipitation tended to be higher in summer or autumn. The monthly variations of DON concentrations were very similar in throughfall and stemflow at both forests, showing an increase at the beginning of the rainy season in March. In contrast, monthly changes of the DOC concentrations in throughfall of the SS and CF were different to those in stemflow. Throughfall DOC concentrations were higher from February to April, while relatively higher DOC concentrations in stemflow were found during September-November period.

  9. ANALYSIS ON THE BEHAVIOR OF PRECIPITATES IN ULTRA-THIN HOT STRIP OF PLAIN LOW CARBON STEEL PRODUCED BY COMPACT STRIP PRODUCTION

    Institute of Scientific and Technical Information of China (English)

    H. Yu; Y.L. Kang; H.B. Dong; D.L. Liu; J. Fu

    2002-01-01

    This paper investigated the mechanism of precipitation and its influence upon prop-erties of ultra-thin hot strips of low carbon steel produced by CSP techniques usingexperiment and thermodynamics theory. The experimental results show that thereare lots of fine and dispersive precipitates in microstructures. By analysis, most ofaluminum nitrides are in grains, while coexisted precipitates of MnS are along grainboundaries. Coexisted precipitates compose cation-vacancy type oxides such as Al2O3in the core, while MnS is at the fringe of surface. The precipitation behavior of AlNand MnS in the hot strip is studied by thermodynamic calculation. At last, implica-tions between strengthening effect and techniques are analyzed using obtained solubilityproducts.

  10. The effect of cobalt and carbon the microstructure and mechanical properties of martensitic precipitation strengthened stainless steels

    Science.gov (United States)

    Komolwit, Piyamanee

    increasing with increasing cobalt content for the same condition. Limited observation on the effects of carbon additions to a 12Cr/12Co/5Mo/4.5Ni martensitic precipitation strengthening stainless steel has been made for carbon levels of 0.005 wt. %, 0.025 wt. % and 0.05 wt. %. A small addition of chromium, one weight percent, to a 0.005C/12Co/5Mo/5Ni martensitic precipitation strengthening stainless steel was found to increase hardness, strength, Charpy impact energy, and ductility. Results on the effects of cobalt, carbon and chromium additions helped in the selection of modified alloys which were used to investigate the effects of composition and heat treatment on strength and toughness. The first set of modified alloys are referred to as the low carbon modified alloys. These alloys have a better Charpy impact energy than the alloys used to investigate the effect of cobalt on strength and the hardness and strength of these alloys are similar to those of alloys used to investigate the effects of cobalt on strength. Fractographs of these alloys show quasi-cleavage fracture, the presence of ductile fracture increases with increasing cobalt content. The martensite start temperature is lowered by the chromium additions and results in the existence of retained austenite even after refrigeration after austenitizing. Refrigeration prior to tempering is not necessary for these alloys to achieve a high yield strength and good Charpy impact energy. The second set of modified alloys are referred to as the carbon-titanium modified alloys. These alloys differ from the first set of modified alloys in that these alloys contain small additions of carbon and titanium and have lower cobalt levels. Lower cobalt levels were required because carbon lowers the martensite start temperature. These alloys have improved Charpy impact energy and ductility. The carbon addition lowers the martensite start temperature and the martensite start temperature of these alloys is sufficiently low that they

  11. Cementation of sand grains based on carbonate precipitation induced by microorganism

    Institute of Scientific and Technical Information of China (English)

    2010-01-01

    Microbes can produce 2 3 CO32-in an environment conductive to precipitation,so the incompact sands will be consolidated.This technology is environmentally friendly not only because it gives strength to the sand body,but also it allows water to penetrate into the sand body,which is unlike silicate cement that will destroy the ecosystem of the earth.After comparing the activity of three kinds of bacteria,the most suitable one was chosen for the study.However,the activity of this bacterium was still not high enough for the purpose,so it was purified.A suitable program for the consolidation and cementation of sands was also found in the experiment.The compressive strength and the porosity of the cemented sand body were tested to characterize the cementation effectiveness.XRD analysis showed that a new phase of calcite was produced between sand grains.The content of calcite was detected by TG.The study showed that the precipitation program was quite important to obtain a sound cemented sand body in addition to the activity of the bacteria.

  12. Crystal structure of Brinzolamide: a carbonic anhydrase inhibitor

    OpenAIRE

    Zheng, Huirong; Lou, Benyong

    2016-01-01

    In crystal structure of the title compound, C12H21N3O5S3 [systematic name: (R)-4-ethyl­amino-2-(3-meth­oxy­prop­yl)-3,4-di­hydro-2H-thieno[3,2-e][1,2]thia­zine-6-sulfonamide 1,1-dioxide], there exist three kinds of hydrogen-bonding inter­actions. The sulfonamide group is involved in hydrogen bonding with the secondary amine and the meth­oxy O atom, resulting in the formation of layers parallel to the bc plane. The layers are linked by an N—H⋯O hydrogen bond involving a sulfonamide O atom as a...

  13. Lanthanide-activated Na5Gd9F32 nanocrystals precipitated from a borosilicate glass: Phase-separation-controlled crystallization and optical property

    International Nuclear Information System (INIS)

    Highlights: • Na5Gd9F32 nanocrystals embedded glass ceramics were fabricated for the first time. • Such glass ceramics were achieved by phase-separation-controlled crystallization. • Elemental mapping evidenced the segregation of activators into the Na5Gd9F32 lattice. • Luminescent color could be tuned by controlling glass crystallization temperature. - Abstract: Lanthanide-activated cubic Na5Gd9F32 nanocrystals were precipitated from a borosilicate glass with a specifically designed composition. The precursor glass is already phase-separated after melt-quenching, which is beneficial to the realization of the controllable glass crystallization for affording desirable size, morphology and activator partition. Elemental mapping in the scanning transmission electron microscopy evidenced that the segregation of lanthanide ions into the Na5Gd9F32 lattice was in situ formed without the requirement of long-range ionic diffusion. Impressively, such fabricated glass ceramic co-doped with Yb3+/Er3+ ions exhibited intense upconversion luminescence, which was about 500 times higher than that of the precursor glass, and its luminescent color could be easily tuned from red to green by controlling glass crystallization temperature. It is anticipated that such phase-separation synthesis strategy with precise control over nanostructure of glass ceramics offer a great opportunity to design other highly transparent nanocomposites with a wide range of tunable optical properties

  14. Synthesis and crystallization behavior of 3 mol% yttria stabilized tetragonal zirconia polycrystals (3Y-TZP) nanosized powders prepared using a simple co-precipitation process

    International Nuclear Information System (INIS)

    Highlights: → The thermal behavior of 3Y-TZP precursor powders had been investigated. → The crystallization behavior of 3Y-TZP nanopowders had been investigated. → The activation energy for crystallization of tetragonal ZrO2 was obtained. → The growth morphology parameter n is approximated as 2.0. → The crystallites show a plate-like morphology. - Abstract: The synthesis and crystallization behavior of 3 mol% yttria stabilized tetragonal zirconia polycrystals (3Y-TZP) nanopowders prepared using a simple co-precipitation process at 348 K and pH = 7 were investigated using differential scanning calorimetry/thermogravimetry (DSC/TG), an X-ray diffractometer (XRD), the Raman spectra, transmission electron microscopy (TEM), selected area electron diffraction (SAED), and an energy dispersive spectrometer (EDS). The activation energy of tetragonal ZrO2 crystallization from 3Y-TZP freeze-dried precursor powders using a non-isothermal method, namely, 169.2 ± 21.9 kJ mol-1, was obtained. The growth morphology parameter n was approximated as 2.0, which indicated that it had a plate-like morphology. The XRD, Raman spectra, and SAED patterns showed that the phase of the tetragonal ZrO2 was maintained at 1273 K. The crystallite size of 3Y-TZP freeze-dried precursor powders calcined at 1273 K for 5 min was 21.3 nm.

  15. Synthesis and crystallization behavior of 3 mol% yttria stabilized tetragonal zirconia polycrystals (3Y-TZP) nanosized powders prepared using a simple co-precipitation process

    Energy Technology Data Exchange (ETDEWEB)

    Hsu, Yu-Wei [Graduate Institute of Applied Science, National Kaohsiung University of Applied Sciences, 415 Chien-Kung Road, Kaohsiung 80782, Taiwan (China); Yang, Ko-Ho, E-mail: yangkoho@cc.kuas.edu.tw [Graduate Institute of Applied Science, National Kaohsiung University of Applied Sciences, 415 Chien-Kung Road, Kaohsiung 80782, Taiwan (China); Department of Mold and Die Engineering, National Kaohsiung University of Applied Sciences, 415 Chien-Kung Road, Kaohsiung 80782, Taiwan (China); Chang, Kuo-Ming [Department of Mechanical Engineering, National Kaohsiung University of Applied Sciences, 415 Chien-Kung Road, Kaohsiung 80782, Taiwan (China); Dental Materials Research Center, National Kaohsiung University of Applied Sciences, 415 Chien-Kung Road, Kaohsiung 80782, Taiwan (China); Yeh, Sung-Wei [Metal Industries Research and Development Centre, 1001 Kaohsiung Highway, Kaohsiung 811, Taiwan (China); Wang, Moo-Chin, E-mail: mcwang@kmu.edu.tw [Department of Fragrance and Cosmetics Science, Kaohsiung Medical University, 100, Shihchuan 1st Road, Kaohsiung 80728, Taiwan (China)

    2011-06-16

    Highlights: > The thermal behavior of 3Y-TZP precursor powders had been investigated. > The crystallization behavior of 3Y-TZP nanopowders had been investigated. > The activation energy for crystallization of tetragonal ZrO{sub 2} was obtained. > The growth morphology parameter n is approximated as 2.0. > The crystallites show a plate-like morphology. - Abstract: The synthesis and crystallization behavior of 3 mol% yttria stabilized tetragonal zirconia polycrystals (3Y-TZP) nanopowders prepared using a simple co-precipitation process at 348 K and pH = 7 were investigated using differential scanning calorimetry/thermogravimetry (DSC/TG), an X-ray diffractometer (XRD), the Raman spectra, transmission electron microscopy (TEM), selected area electron diffraction (SAED), and an energy dispersive spectrometer (EDS). The activation energy of tetragonal ZrO{sub 2} crystallization from 3Y-TZP freeze-dried precursor powders using a non-isothermal method, namely, 169.2 {+-} 21.9 kJ mol{sup -1}, was obtained. The growth morphology parameter n was approximated as 2.0, which indicated that it had a plate-like morphology. The XRD, Raman spectra, and SAED patterns showed that the phase of the tetragonal ZrO{sub 2} was maintained at 1273 K. The crystallite size of 3Y-TZP freeze-dried precursor powders calcined at 1273 K for 5 min was 21.3 nm.

  16. Calcium carbonate crystallizations on hypogean mural paintings: a pilot study of monitoring and diagnostics in Roman catacombs

    Science.gov (United States)

    Tapete, D.; Fratini, F.; Mazzei, B.; Camaiti, M.; Cantisani, E.; Riminesi, C.; Manganelli Del Fà, R.; Cuzman, O.; Tiano, P.

    2012-04-01

    One of the deterioration processes affecting mural paintings and rock surfaces within manmade hypogea consists in the formation of calcium carbonate crystallizations, which can create thick coverage and incrustations, even in some cases speleothems. These chemical reactions necessarily require the availability of calcium sources, which can be also of anthropogenic origin (e.g., lime-based mortars). Microclimate parameters also represent environmental forcing factors, on which the morphology and the degree of crystallinity of the precipitated carbonates depend. Understanding past/recent dynamics of carbonate precipitation implies a deep knowledge of the relationships between the exposed surfaces and the microclimate conditions, the impacts of external factors (e.g., groundwater infiltration and percolation from the overlying soil) and how they change over time. This is particularly fundamental for the preservation of hypogean sites which have not comparison with other typologies of environment due to their uniqueness, such as the ancient catacombs carved underneath the suburbs of Rome (Italy), since the 2nd century AD. In this paper we present the multidisciplinary methodological approach designed for the instrumental monitoring of the microphysical environment of the Catacombs of Saints Mark, Marcellian and Damasus, in the framework of the co-operation between the Institute for the Conservation and Valorization of Cultural Heritage and Pontifical Commission for Sacred Archaeology, Vatican, on the project HYPOGEA. Temperature inside the catacomb and on the surfaces, air relative humidity and CO2 concentration are the main of the parameters continuously measured by means of data loggers installed within the cubicles. Contemporarily, standardized methods of photographic documentation and digital micro-photogrammetry are used for change detection analysis of the painted surfaces and ancient plasters, as well as of the test areas purposely realized by applying fresh

  17. A single crystal carbon self-sputtering simulation

    International Nuclear Information System (INIS)

    Carbon bombardment of graphite and diamond is investigated by molecular dynamics simulations using a many-body potential to describe the low energy interactions splined to a Moliere potential which describes the hard collisions. It is found that no ejection takes place from the perfect graphite {1000} face at bombardment energies of 100 eV and that at normal incidence the yield is below 1% up to 600 eV. At oblique incidence corresponding to the maximum yield angle, the yield can be in excess of ten times that at normal incidence and a much larger proportion of dimer and trimer molecules are ejected. The bulk terminated diamond surfaces are found to be less resistant to erosion than graphite with as much as 23% of material ejected at normal incidence being in the form of dimers. (orig.)

  18. Carbon Mineralization by Aqueous Precipitation for Beneficial Use of CO2 from Flue Gas. Phase I. Final Topical Report

    International Nuclear Information System (INIS)

    Calera's innovative Mineralization via Aqueous Precipitation (MAP) technology for the capture and conversion of CO2 to useful materials for use in the built environment was further developed and proven in the Phase 1 Department of Energy Grant. The process was scaled to 300 gallon batch reactors and subsequently to Pilot Plant scale for the continuous production of product with the production of reactive calcium carbonate material that was evaluated as a supplementary cementitious material (SCM). The Calera SCM(trademark) was evaluated as a 20% replacement for ordinary portland cement and demonstrated to meet the industry specification ASTM 1157 which is a standard performance specification for hydraulic cement. The performance of the 20% replacement material was comparable to the 100% ordinary portland cement control in terms of compressive strength and workability as measured by a variety of ASTM standard tests. In addition to the performance metrics, detailed characterization of the Calera SCM was performed using advanced analytical techniques to better understand the material interaction with the phases of ordinary portland cement. X-ray synchrotron diffraction studies at the Advanced Photon Source in Argonne National Lab confirmed the presence of an amorphous phase(s) in addition to the crystalline calcium carbonate phases in the reactive carbonate material. The presence of carboaluminate phases as a result of the interaction of the reactive carbonate materials with ordinary portland cement was also confirmed. A Life Cycle Assessment was completed for several cases based on different Calera process configurations and compared against the life cycle of ordinary portland cement. In addition to the materials development efforts, the Calera technology for the production of product using an innovative building materials demonstration plant was developed beyond conceptual engineering to a detailed design with a construction schedule and cost estimate.

  19. Evolution of Microstructure and Precipitation State during Thermomechanical Processing of a Low Carbon Microalloyed Steel

    OpenAIRE

    Valles, P.; Gómez, Manuel; Medina, Sebastián F.; Pastor, A.; Vilanova, O.

    2012-01-01

    The increasing demand of sources of energy such as oil and natural gas induces at the steel industry a development on low carbon microalloyed steels for pipeline applications in order to achieve excellent mechanical properties of strength and toughness at a reduced cost. To obtain an adequate fine-grained final structure, the strict control of thermomechanical processing and accelerated cooling is crucial. Depending on the thermomechanical processing conditions and chemical composition, pipel...

  20. Origin of Magnetite Crystals in Martian Meteorite ALH84001 Carbonate Disks

    Science.gov (United States)

    Thomas-Keprta, K.L.; Clemett, S.J.; McKay, D.S.; Gibson, E. K.; Wentworth, S. J.

    2010-01-01

    Martian meteorite ALH84001 preserves evidence of interaction with aqueous fluids while on Mars in the form of microscopic carbonate disks which are believed to have precipitated approx.3.9 Ga ago at beginning of the Noachian epoch. Intimately associated within and throughout these carbonate disks are nanocrystal magnetites (Fe3O4) with unusual chemical and physical properties, whose origins have become the source of considerable debate. One group of hypotheses argues that these Fe3O4 are the product of partial thermal decomposition of the host carbonate. Alternatively, the origins of Fe3O4 and carbonate may be unrelated; that is, from the perspective of the carbonate the magnetite is allochthonous. We have sought to resolve between these hypotheses through the detailed characterized of the compositional and structural relationships of the carbonate disks and associated magnetites with the orthopyroxene matrix in which they are embedded [1]. We focus this discussion on the composition of ALH84001 magnetites and then compare these observations with those from our thermal decomposition studies of sideritic carbonates under a range of plausible geological heating scenarios.

  1. Structural, elastic and electronic Properties of isotropic cubic crystals of carbon and silicon nanotubes : Density functional based tight binding calculations.

    Directory of Open Access Journals (Sweden)

    Alexander L. Ivanovskii

    2008-01-01

    Full Text Available Atomic models of cubic crystals (CC of carbon and graphene-like Si nanotubes are offered and their structural, cohesive, elastic and electronic properties are predicted by means of the DFTB method. Our main findings are that the isotropic crystals of carbon nanotubes adopt a very high elastic modulus B and low compressibility β, namely B = 650 GPa, β = 0.0015 1/GPa. In addition, these crystals preserve the initial conductivity type of their “building blocks”, i.e. isolated carbon and Si nanotubes. This feature may be important for design of materials with the selected conductivity type.

  2. Composition and timing of carbonate vein precipitation within the igneous basement of the Early Cretaceous Shatsky Rise, NW Pacific

    Science.gov (United States)

    Geldmacher, J.; Li, S.; Hauff, F. F.; Garbe-Schoenberg, C.; Yu, S.; Zhao, S.; Rausch, S.

    2013-12-01

    Shatsky Rise is an Early Cretaceous large igneous province located in the NW Pacific ca. 1500 km east of Japan and is the third-largest oceanic plateau on Earth (after Ontong Java and Kerguelen). Numerous calcium carbonate veins were recovered from the igneous basement of Shatsky Rise during Integrated Ocean Drilling Program Expedition 324 (Sager et al., 2010). The chemical (Sr/Ca, Mg/Ca) and isotopic (87Sr/86Sr, 143Nd/144Nd, δ18O, δ13C) compositions of these veins were determined to constrain the timing of vein formation and to provide valuable data for the reconstruction of past seawater composition. A dominant control of seawater chemistry on calcite composition is evident for most investigated vein samples with varying compositional contribution from the basaltic basement. The Sr/Ca ratio of the vein calcite is positively correlated with Mg/Ca and with δ18O, indicating warmer/colder precipitation temperatures with decreasing/increasing Sr/Ca (and Mg/Ca) ratios, respectively. Distinctly higher formation temperatures (as inferred from oxygen isotope ratios) indicative of hydrothermal vein formation are only observed at one site (Site U1350, drilled into the central part of Shatsky Rise). The highest 87Sr/86Sr ratios (least basement influence) of vein samples at each drill site range form 0.707264 to 0.707550 and are believed to best reflect contemporaneous Early Cretaceous seawater composition. In principle, age information can be deduced by correlating these ratios with the global seawater Sr isotope evolution. Since the Sr isotopic composition of seawater has fluctuated three times between the early and mid Cretaceous (McArthur et al., 2001) no unambiguous precipitation ages can be constrained by this method and vein precipitation could have occurred at any time between ˜80 and 140 Ma. However, based on combined chemical and isotopic data and correlations of vein composition with formation depth and inferred temperature, we argue for a rather early

  3. Synthesis and electrochemical characterization of LiNi0.5Mn1.5O4 by one-step precipitation method with ammonium carbonate as precipitating agent

    International Nuclear Information System (INIS)

    Highlights: → Ammonium carbonate is used as the precipitating agent of synthesizing LiNi0.5Mn1.5O4 for the first time. → All the metal ions precipitated in one time, no washing process is needed. → Effect of concentration and hydrothermal on the materials are concerned. → The obtained material shows regular quasi-spherical. → The synthesized materials behave excellent electrochemical properties. - Abstract: Spinel LiNi0.5Mn1.5O4 materials are synthesized by one-step precipitation method. Ammonium carbonate is used as the precipitating agent to obtain a more precise feed ratio without recourse to traditional washing. After annealing at high temperature, the spherical particles become angular and show high levels of crystallinity. The synthesized samples are evaluated using powder X-ray diffraction, scanning electron microscopy, and electrochemical testing. The samples synthesized with different metal ion concentrations yield different morphologies and rate performances. The sample synthesized with 0.2 mol L-1 gives the most uniform particle distribution and the best electrochemical performance. The specific discharge capacity values of the sample at 10 and 15 C are as high as 109.5 and 88.7 mAh g-1, respectively. After the high-rate cycling, its discharge capacity at 0.2 C can be reverted to 97.67% of its initial capacity.

  4. Synthesis of beta carbon nitride nanosized crystal through mechanochemical reaction

    CERN Document Server

    Yin Long Wei; Liu Yu Xian; Sui Jin Ling; Wang Jing Min

    2003-01-01

    Nanosized beta carbon nitride (beta-C sub 3 N sub 4), of grain size several tens of nanometres, has been synthesized by mechanochemical reaction processing. The low-cost synthetic method developed facilitates the novel and effective synthesis of nanosized crystalline beta-C sub 3 N sub 4 (a = 6.36 A, c = 4.648 A) powders. The graphite powders were first milled to a nanoscale state, then the nanosized graphite powders were milled in an atmosphere of NH sub 3 gas. It was found that nanosized beta-C sub 3 N sub 4 was formed after high-energy ball milling under an NH sub 3 atmosphere. After thermal annealing, the shape of the beta-C sub 3 N sub 4 changes from flake-like to sphere-like. The nanosized beta-C sub 3 N sub 4 formed was characterized by x-ray diffraction, Fourier transformation infrared spectroscopy, and transmission electron microscopy. A solid-gas reaction mechanism was proposed for the formation of nanosized beta-C sub 3 N sub 4 at room temperature induced by mechanochemical activation.

  5. Liquid phase adsorption of Crystal violet onto activated carbons derived from male flowers of coconut tree.

    Science.gov (United States)

    Senthilkumaar, S; Kalaamani, P; Subburaam, C V

    2006-08-25

    Adsorption of Crystal violet, a basic dye onto phosphoric and sulphuric acid activated carbons (PAAC and SAAC), prepared from male flowers coconut tree has been investigated. Equilibrium data were successfully applied to study the kinetics and mechanism of adsorption of dye onto both the carbons. The kinetics of adsorption was found to be pseudo second order with regard to intraparticle diffusion. The pseudo second order is further supported by the Elovich model, which in turn intensifies the fact of chemisorption of dye onto both the carbons. Quantitative removal of dye at higher initial pH of dye solution reveals the basic nature of the Crystal violet and acidic nature of the activated carbons. Influence of temperature on the removal of dye from aqueous solution shows the feasibility of adsorption and its endothermic nature. Mass transfer studies were also carried out. The adsorption capacities of both the carbons were found to be 60.42 and 85.84 mg/g for PAAC and SAAC, respectively. Langmuir's isotherm data were used to design single-stage batch adsorption model.

  6. Carbon Mineralization by Aqueous Precipitation for Beneficial Use of CO2 from Flue Gas

    Energy Technology Data Exchange (ETDEWEB)

    Devenney, Martin; Gilliam, Ryan; Seeker, Randy

    2013-08-01

    The objective of this project is to demonstrate an innovative process to mineralize CO2 from flue gas directly to reactive carbonates and maximize the value and versatility of its beneficial use products. The program scope includes the design, construction, and testing of a CO2 Conversion to Material Products (CCMP) Pilot Demonstration Plant utilizing CO2 from the flue gas of a power production facility in Moss Landing, CA. This topical report covers Subphase 2a which is the design phase of pilot demonstration subsystems. Materials of construction have been selected and proven in both lab scale and prototype testing to be acceptable for the reagent conditions of interest. The target application for the reactive carbonate material has been selected based upon small-scale feasibility studies and the design of a continuous fiber board production line has been completed. The electrochemical cell architecture and components have been selected based upon both lab scale and prototype testing. The appropriate quality control and diagnostic techniques have been developed and tested along with the required instrumentation and controls. Finally the demonstrate site infrastructure, NEPA categorical exclusion, and permitting is all ready for the construction and installation of the new units and upgrades.

  7. Carbon Mineralization by Aqueous Precipitation for Beneficial Use of CO2 from Flue Gas

    Energy Technology Data Exchange (ETDEWEB)

    Devenney, Martin; Gilliam, Ryan; Seeker, Randy

    2014-06-01

    The objective of this project is to demonstrate an innovative process to mineralize CO2 from flue gas directly to reactive carbonates and maximize the value and versatility of its beneficial use products. The program scope includes the design, construction, and testing of a CO2 Conversion to Material Products (CCMP) Pilot Demonstration Plant utilizing CO2 from the flue gas of a power production facility in Moss Landing, CA as well as flue gas from coal combustion. This topical report covers Phase 2b, which is the construction phase of pilot demonstration subsystems that make up the integrated plant. The subsystems included are the mineralization subsystem, the Alkalinity Based on Low Energy (ABLE) subsystem, the waste calcium oxide processing subsystem, and the fiber cement board production subsystem. The fully integrated plant is now capable of capturing CO2 from various sources (gas and coal) and mineralizing into a reactive calcium carbonate binder and subsequently producing commercial size (4ftx8ft) fiber cement boards. The topical report provides a description of the “as built” design of these subsystems and the results of the commissioning activities that have taken place to confirm operability. At the end of Phase 2b, the CCMP pilot demonstration is fully ready for testing.

  8. Precipitation in solid solution and structural transformations in single crystals of high rhenium ruthenium-containing nickel superalloys at high-temperature creep

    Energy Technology Data Exchange (ETDEWEB)

    Alekseev, A.A.; Petrushin, N.V.; Zaitsev, D.V.; Treninkov, I.A.; Filonova, E.V. [All-Russian Scientific Research Institute of Aviation Materials (VIAM), Moscow (Russian Federation)

    2010-07-01

    The phase composition and structure of single crystals of two superalloys (alloy 1 and alloy 2) were investigated in this work. For alloy 1 (Re - 9 wt%) the kinetics of precipitation in solid solution at heat treatment (HT) was investigated. TEM and X-Ray examinations have revealed that during HT rhombic phase (R-phase) precipitation (Immm class (BCR)) occurs. The TTT diagram is plotted, it contains the time-temperature area of the existence of R-phase particles. The element content of R-phase is identified (at. %): Re- 51.5; Co- 23.5; Cr- 14.8; Mo- 4.2; W- 3.3; Ta- 2.7. For alloy 2 (Re - 6.5 wt %, Ru - 4 wt %) structural transformations at high-temperature creep are investigated. By dark-field TEM methods it is established, that in alloy 2 the additional phase with a rhombic lattice is formed during creep. Particles of this phase precipitate in {gamma}-phase and their quantity increases during high-temperature creep. It is revealed that during creep 3-D dislocation network is formed in {gamma}-phase. At the third stage of creep the process of inversion structure formation is observed in the alloy, i.e. {gamma}'-phase becomes a matrix. Thus during modeling creep the volume fraction of {gamma}'-phase in the samples increases from 30% (at creep duration of 200 hrs) up to 55% (at 500 hrs). The processes of structure formation in Re and Ru-containing nickel superalloys are strongly affected by decomposition of solid solution during high-temperature creep that includes precipitation of additional TCP-phases. (orig.)

  9. Metagenome-based diversity analyses suggest a significant contribution of non-cyanobacterial lineages to carbonate precipitation in modern microbialites

    Directory of Open Access Journals (Sweden)

    Purificacion eLopez-Garcia

    2015-08-01

    Full Text Available Cyanobacteria are thought to play a key role in carbonate formation due to their metabolic activity, but other organisms carrying out oxygenic photosynthesis (photosynthetic eukaryotes or other metabolisms (e.g. anoxygenic photosynthesis, sulfate reduction, may also contribute to carbonate formation. To obtain more quantitative information than that provided by more classical PCR-dependent methods, we studied the microbial diversity of microbialites from the Alchichica crater lake (Mexico by mining for 16S/18S rRNA genes in metagenomes obtained by direct sequencing of environmental DNA. We studied samples collected at the Western (AL-W and Northern (AL-N shores of the lake and, at the latter site, along a depth gradient (1, 5, 10 and 15 m depth. The associated microbial communities were mainly composed of bacteria, most of which seemed heterotrophic, whereas archaea were negligible. Eukaryotes composed a relatively minor fraction dominated by photosynthetic lineages, diatoms in AL-W, influenced by Si-rich seepage waters, and green algae in AL-N samples. Members of the Gammaproteobacteria and Alphaproteobacteria classes of Proteobacteria, Cyanobacteria and Bacteroidetes were the most abundant bacterial taxa, followed by Planctomycetes, Deltaproteobacteria (Proteobacteria, Verrucomicrobia, Actinobacteria, Firmicutes and Chloroflexi. Community composition varied among sites and with depth. Although cyanobacteria were the most important bacterial group contributing to the carbonate precipitation potential, photosynthetic eukaryotes, anoxygenic photosynthesizers and sulfate reducers were also very abundant. Cyanobacteria affiliated to Pleurocapsales largely increased with depth. Scanning electron microscopy (SEM observations showed considerable areas of aragonite-encrusted Pleurocapsa-like cyanobacteria at microscale. Multivariate statistical analyses showed a strong positive correlation of Pleurocapsales and Chroococcales with aragonite formation at

  10. DISLOCATION PINNING IN HIGH TEMPERATURE DEFORMED Ni3(Al,Ti) SINGLE CRYSTALS CONTAINING DISORDERED γ PRECIPITATES

    Institute of Scientific and Technical Information of China (English)

    W.H. Tian; M. Nemoto

    2006-01-01

    A transmission electron microscopy (TEM) investigation has been performed on the dislocation pinning in LI2-ordered Ni3(Al, Ti) containing disordered γ precipitates. The morphology of deformation induced dislocations in the γ' base alloys containing fine dispersion of disordered γ was investigated by means of weak-beam electron microscopy. The superdislocations are strongly attracted to the disordered particles and dissociate on the (111) plane in the γ particles, while they dissociate on the (010) plane in the γ' matrix. The disordered γ precipitates play an important role as a pinning point during the cross-slip of superdislocations from (111) to (010) planes in the γ'matrix and restrain the cross-slip of superdislocations. The interaction of superdislocations with disordered particles causes the formation of superkinks, jogs and closed loops.

  11. Sizeable magnetic circular dichroism of artificially precipitated Co clusters in amorphous carbon

    Directory of Open Access Journals (Sweden)

    H. S. Hsu

    2012-09-01

    Full Text Available This study examines sizeable magnetic circular dichroism (MCD in Co(20%-doped amorphous carbon (a-C films. While as-grown films exhibit a non-detectable MCD signal, films that undergo rapid thermal annealing (RTA at 600°C in a vacuum yield broad MCD spectra with a large amplitude of ∼3.9 × 104 deg/cm in saturation field 0.78 T at the σ-σ* gap transition (∼5.5 eV. In such films after RTA, the metastable Co-C bonding is decomposed and suitable Co nanoparticles/a-C interfaces are thus formed. Our results indicate that the large change in MCD is contributed from Co nanoparticles and associated with the spin-dependent electronic structure at the Co/a-C interfaces.

  12. Precipitation Behaviors of Nanometer-sized Carbides in a Niobium-Titanium Contained Low-Carbon Steel%含 Nb -Ti 低碳微合金钢纳米碳化物析出行为

    Institute of Scientific and Technical Information of China (English)

    李小琳; 王昭东

    2015-01-01

    采用热膨胀仪、显微硬度计和透射电镜研究了等温温度对 Nb -Ti 微合金钢组织性能及析出行为的影响规律.结果表明,在不同温度下等温淬火均得到铁素体与马氏体的双相组织,且随着等温温度的降低,铁素体的体积分数逐渐增大.实验钢中存在两种主要的析出形态,分别为相间析出和弥散析出,且随着等温温度的降低,析出形态逐渐从相间析出向弥散析出转变.通过 HRTEM确定相间析出碳化物具有 NaCl 型晶体结构,晶格常数为0.432 nm,且与铁素体基体满足 Baker -Nutting (B -N)关系.铁素体相的维氏硬度随着等温温度的降低而逐渐增大.%The microstructure,mechanical properties and precipitation behaviors in a low carbon Nb-Ti micro-alloyed steel were investigated using the dilatometer,Vickers-hardness tester and transmission electron microscope.The results showed that the microstructure of the experimental steel treated by an isothermal quenching process under different temperatures all mainly consisted of ferrite and martensite phases.The volume fraction of ferrite phase increased with the decrease of the isothermal temperature.Both of the interphase precipitation and supersaturated precipitation of carbides appeared in the samples treated by the isothermal quenching process.Along with the decrease of isothermal temperature,the precipitation form gradually changed from the interphase precipitation to supersaturated precipitation.Furthermore,the interphase-precipitated carbides had a NaCl-type crystal structure with a lattice parameter of 0.432 nm and obeyed the Baker -Nutting (B -N)orientation relationship with respect to the ferrite matrix which confirmed by HRTEM. The Vickers-hardness of the ferrite increased with the decrease of the isothermal temperature.

  13. Electrochemical quartz crystal microbalance (EQCM) study of ion dynamics in nanoporous carbons.

    Science.gov (United States)

    Tsai, Wan-Yu; Taberna, Pierre-Louis; Simon, Patrice

    2014-06-18

    Electrochemical quartz crystal microbalance (EQCM) and cyclic voltammetry (CV) measurements were used to characterize ion adsorption in carbide-derived carbon (CDC) with two different average pore sizes (1 and 0.65 nm), from neat and solvated 1-Ethyl-3-methylimidazolium bis(trifluoromethanesulfonyl)imide (EMI-TFSI) electrolytes. From the electrode mass change in neat EMI-TFSI, it was shown that one net charge stored corresponds almost to one single ion at high polarization; in that case, no ion-pairing or charge screening by co-ions were observed. In 2 M EMI-TFSI in acetonitrile electrolyte, experimental solvation numbers were estimated for EMI(+) cation, showing a partial desolvation when cations were adsorbed in confined carbon pores. The extent of desolvation increased when decreasing the carbon pore size (from 1 down to 0.65 nm). The results also suggest that EMI(+) cation owns higher mobility than TFSI(-) anion in these electrolytes.

  14. The study of crystallization and interfacial morphology in polymer/carbon nanotube composites

    Science.gov (United States)

    Minus, Marilyn Lillith

    This study illustrates the ability of SWNT to nucleate and template polymer crystallization and orientation, and produce materials with improved properties and unique polymer morphologies. This research work focuses primarily on the physical interaction between single-wall carbon nanotubes (SWNT) and the flexible polymer system polyvinyl alcohol (PVA). Polymer crystallization in the near vicinity of SWNT (interphase) has been studied to understand the capability of SWNT in influence polymer morphology in bulk films and fibers. Fibrillar crystallization was achieved by shearing PVA/SWNT dispersions and resulted in the formation of oriented PVA/SWNT fibers or ribbons, while PVA solutions produce unoriented fibers. PVA single crystals were grown in PVA solutions as well as PVA/SWNT dispersions over a period of several months at room temperature (25°C). PVA single crystal growth in PVA/SWNT dispersions is templated by SWNT, and these crystals show the presence of new morphologies for PVA. PVA single crystals of differing morphology were also grown at elevated temperatures, and show morphology dependant electron beam irradiation resistance. Gel-spinning was used to produce PVA, and PVA/SWNT fibers where, PVA crystallization in the bulk fiber was observed. With 1 wt% SWNT loading in PVA, the fiber tensile strength increased from 1.6 GPa for the control PVA to 2.6 GPa for PVA/SWNT. Analysis of this data suggests stress of up to ˜120 GPa on the SWNT. This is the highest reported stress on the SWNT to date and confirm excellent reinforcement and load transfer of SWNT in the PVA matrix. Raman spectroscopy data show high SWNT alignment in the fiber where the I0*/I90* ratio is measured to be 106. High-resolution transmission electron microscopy (HR-TEM) is used to characterize polymer morphology near the polymer-SWNT interface for PVA/SWNT fibers. HR-TEM studies of Polymer/CNT composites show distinct morphological differences at the polymer-SWNT interface/interphase for

  15. Arsenic species interactions with a porous carbon electrode as determined with an electrochemical quartz crystal microbalance

    Science.gov (United States)

    Morallón, Emilia; Arias-Pardilla, Joaquín; Calo, J.M.; Cazorla-Amorós, D.

    2009-01-01

    The interactions of arsenic species with platinum and porous carbon electrodes were investigated with an electrochemical quartz crystal microbalance (EQCM) and cyclic voltammetry in alkaline solutions. It is shown that the redox reactions in arsenic-containing solutions, due to arsenic reduction/deposition, oxidation/desorption, and electrocatalyzed oxidation by Pt can be readily distinguished with the EQCM. This approach was used to show that the arsenic redox reactions on the carbon electrode are mechanistically similar to that on the bare Pt electrode. This could not be concluded with just classical cyclic voltammetry alone due to the obfuscation of the faradaic features by the large capacitative effects of the carbon double layer. For the porous carbon electrode, a continual mass loss was always observed during potential cycling, with or without arsenic in the solution. This was attributed to electrogasification of the carbon. The apparent mass loss per cycle was observed to decrease with increasing arsenic concentration due to a net mass increase in adsorbed arsenic per cycle that increased with arsenic concentration, offsetting the carbon mass loss. Additional carbon adsorption sites involved in arsenic species interactions are created during electrogasification, thereby augmenting the net uptake of arsenic per cycle. It is demonstrated that EQCM, and in particular the information given by the behavior of the time derivative of the mass vs. potential, or massogram, is very useful for distinguishing arsenic species interactions with carbon electrodes. It may also prove to be effective for investigating redox/adsorption/desorption behavior of other species in solution with carbon materials as well. PMID:20161369

  16. Arsenic species interactions with a porous carbon electrode as determined with an electrochemical quartz crystal microbalance.

    Science.gov (United States)

    Morallón, Emilia; Arias-Pardilla, Joaquín; Calo, J M; Cazorla-Amorós, D

    2009-06-30

    The interactions of arsenic species with platinum and porous carbon electrodes were investigated with an electrochemical quartz crystal microbalance (EQCM) and cyclic voltammetry in alkaline solutions. It is shown that the redox reactions in arsenic-containing solutions, due to arsenic reduction/deposition, oxidation/desorption, and electrocatalyzed oxidation by Pt can be readily distinguished with the EQCM. This approach was used to show that the arsenic redox reactions on the carbon electrode are mechanistically similar to that on the bare Pt electrode. This could not be concluded with just classical cyclic voltammetry alone due to the obfuscation of the faradaic features by the large capacitative effects of the carbon double layer.For the porous carbon electrode, a continual mass loss was always observed during potential cycling, with or without arsenic in the solution. This was attributed to electrogasification of the carbon. The apparent mass loss per cycle was observed to decrease with increasing arsenic concentration due to a net mass increase in adsorbed arsenic per cycle that increased with arsenic concentration, offsetting the carbon mass loss. Additional carbon adsorption sites involved in arsenic species interactions are created during electrogasification, thereby augmenting the net uptake of arsenic per cycle.It is demonstrated that EQCM, and in particular the information given by the behavior of the time derivative of the mass vs. potential, or massogram, is very useful for distinguishing arsenic species interactions with carbon electrodes. It may also prove to be effective for investigating redox/adsorption/desorption behavior of other species in solution with carbon materials as well.

  17. Effects of Strain-Induced Crystallization on Mechanical Properties of Elastomeric Composites Containing Carbon Nanotubes and Carbon Black

    Energy Technology Data Exchange (ETDEWEB)

    Sung, Jong Hwan; Ryu, Sang Ryeoul; Lee, Dong Joo [Yeungnam University, Gyeongsan (Korea, Republic of)

    2011-09-15

    The effects of strain-induced crystallization (SIC) on the mechanical properties of elastomeric composites as functions of extension ratio ({lambda}), multi walled carbon nanotube (CNT) content, and carbon black (CB) content are investigated. The differential scanning calorimetry (DSC) analysis shows that the degree of crystallinity increases with the increase in the CB and CNT content. As {lambda} increases, the glass transition temperature (Tg) of the composites increases, and the latent heat of crystallization (LHc) of the composites is maximum at {lambda}=1.5. It is found that the mechanical properties have a linear relation with LHc, depending on the CNT content. According to the TGA (thermogravimetric analysis), the weight loss of the composite matrix is 94.3% and the weight of the composites decreases with the filler content. The ratio of tensile modulus (E{sub comp}/ E{sub matrix}) is higher than that of tensile strength ({sigma}{sub comp}/ {sigma}{sub matrix}) because of the CNT orientation inside the elastomeric composites.

  18. The microstructural record of porphyroclasts and matrix of serpentinite mylonites – from brittle and crystal-plastic deformation to dissolution-precipitation creep

    Directory of Open Access Journals (Sweden)

    J. Bial

    2013-04-01

    Full Text Available We examine the microfabric development in high-pressure, low-temperature metamorphic serpentinite mylonites exposed in the Erro-Tobbio Unit (Voltri Massif, Italy using polarization microscopy and electron microscopy (SEM/EBSD, EMP. The mylonites are derived from mantle peridotites, were serpentinized at the ocean floor and underwent high pressure metamorphism during Alpine subduction. They contain diopside and olivine porphyroclasts embedded in a fine-grained matrix essentially consisting of antigorite. The porphyroclasts record brittle and crystal-plastic deformation of the original peridotites in the upper mantle at stresses of a few hundred MPa. After the peridotites became serpentinized, deformation occurred mainly by dissolution-precipitation creep resulting in a foliation with flattened olivine grains at phase boundaries with antigorite, crenulation cleavages and olivine and antigorite aggregates in strain shadows next to porphyroclasts. It is suggested that the fluid was provided by dehydration reactions of antigorite forming olivine and enstatite during subduction and prograde metamorphism. At sites of stress concentration around porphyroclasts antigorite reveals an associated SPO and CPO, characteristically varying grain sizes and sutured grain boundaries, indicating deformation by dislocation creep. Stresses were probably below a few tens of MPa in the serpentinites, which was not sufficiently high to allow for crystal-plastic deformation of olivine at conditions at which antigorite is stable. Accordingly, any intragranular deformation features of the newly precipitated olivine in strain shadows are absent. The porphyroclast microstructures are not associated with the microstructures of the mylonitic matrix, but are inherited from an independent earlier deformation. The porphyroclasts record a high-stress deformation in the upper mantle of the oceanic lithosphere probably related to rifting processes, whereas the antigorite matrix

  19. The local crystallization in nanoscale diamond-like carbon films during annealing

    International Nuclear Information System (INIS)

    The local crystallization during annealing at 600 °C in nanoscale diamond-like carbon coatings films grown by pulsed vacuum-arc deposition method was observed using modern techniques of high-resolution transmission electron microscopy. The crystallites formed by annealing have a face-centred cubic crystal structure and grow in the direction [01¯1¯] as a normal to the film surface. The number and size of the crystallites depend on the initial values of the intrinsic stresses before annealing, which in turn depend on the conditions of film growth. The sizes of crystallites are 10 nm for films with initial compressive stresses of 3 GPa and 17 nm for films with initial compressive stresses of 12 GPa. Areas of local crystallization arising during annealing have a structure different from the graphite. Additionally, the investigation results of the structure of nanoscale diamond-like carbon coatings films using Raman spectroscopy method are presented, which are consistent with the transmission electron microscopy research results

  20. The promotion of Ru on topologically close-packed phase precipitation in the high Cr-containing (∼9wt.%) nickel-base single crystal superalloy

    International Nuclear Information System (INIS)

    The partitioning behaviors of alloying elements Cr, Co, Al, Ta, etc. on the γ and γ′ phases of high Cr-containing (∼9wt.%) nickel-base single crystal superalloys have been investigated with and without the addition of 3wt.% Ru. The “reverse partitioning effect” occurs, which means that the addition of Ru causes the partition of Cr and Co into γ′ phase, while Al an Ta concentrate into γ matrix. However, Ru promotes the precipitation of topologically close-packed (TCP) phases, since the diffusion coefficient between the TCP phase and the matrix interface increases with the diffusion behaviors of refractory elements. For the coarsening and slightly rafting of γ′ phases, the increase of elemental diffusion plays much more important role in its kinetic process than the decrease of lattice misfit. - Highlights: • The high Cr-containing (∼9wt.%) superalloys are chosen in this study. • The “reverse partitioning” behavior occurs with the addition of 3wt.% Ru. • Ru promotes the precipitation of topologically close-packed (TCP) phases. • Ru accelerates the diffusion process of alloying elements. • Increase of elemental diffusion plays important role in coarsening of γʹ phases

  1. The promotion of Ru on topologically close-packed phase precipitation in the high Cr-containing (∼9wt.%) nickel-base single crystal superalloy

    Energy Technology Data Exchange (ETDEWEB)

    Lv, Xianzi [Key Laboratory for Liquid-Solid Structural Evolution & Processing of Materials, Ministry of Education, Shandong University, Jinan 250061 (China); Zhang, Jianxin, E-mail: jianxin@sdu.edu.cn [Key Laboratory for Liquid-Solid Structural Evolution & Processing of Materials, Ministry of Education, Shandong University, Jinan 250061 (China); Feng, Qiang [State Key Laboratory for Advanced Metals and Material, University of Science and Technology Beijing, Beijing 100083 (China); National Center for Materials Service Safety, University of Science and Technology Beijing, Beijing 100083 (China)

    2015-11-05

    The partitioning behaviors of alloying elements Cr, Co, Al, Ta, etc. on the γ and γ′ phases of high Cr-containing (∼9wt.%) nickel-base single crystal superalloys have been investigated with and without the addition of 3wt.% Ru. The “reverse partitioning effect” occurs, which means that the addition of Ru causes the partition of Cr and Co into γ′ phase, while Al an Ta concentrate into γ matrix. However, Ru promotes the precipitation of topologically close-packed (TCP) phases, since the diffusion coefficient between the TCP phase and the matrix interface increases with the diffusion behaviors of refractory elements. For the coarsening and slightly rafting of γ′ phases, the increase of elemental diffusion plays much more important role in its kinetic process than the decrease of lattice misfit. - Highlights: • The high Cr-containing (∼9wt.%) superalloys are chosen in this study. • The “reverse partitioning” behavior occurs with the addition of 3wt.% Ru. • Ru promotes the precipitation of topologically close-packed (TCP) phases. • Ru accelerates the diffusion process of alloying elements. • Increase of elemental diffusion plays important role in coarsening of γʹ phases.

  2. Single-walled Carbon Nanotubes Regularly Aligned in Channels of Zeolite Single Crystal

    Institute of Scientific and Technical Information of China (English)

    Zi Kang Tang; Handong Sun; Jiannong Wang

    2000-01-01

    @@ We report the synthesis of single-wall carbon nanotubes (SWCNs) formed in 1-nm-sized channels of zeolite crystal by pyrolysis of tripropylamine molecules. The SWCNs are mono-sized and parallelly aligned along the crystal direction. In the present paper, we report the polarized Raman spectra measured for the wellaligned SWCNs, which gives us information about structural symmetry. Electrical transport properties of the SWNTs are measured in the temperature range of 0.3 K ~ 300 K. The conductivity of the SWCNs is monotonically decreased with decreasing temperature. The observed temperature dependence of zero-field conductance, In(σ) ~ 1/√T, could be explained well in terms of electron localization caused by imperfections and impurities in the nanotubes.

  3. Crystal structure of di-chlorido-bis-(dimethyl N-cyano-dithio-imino-carbonate)cobalt(II).

    Science.gov (United States)

    Diop, Mouhamadou Birame; Diop, Libasse; Oliver, Allen G

    2016-01-01

    The structure of the mononuclear title complex, [{(H3CS)2C=NC  N}2CoCl2], consists of a Co(II) atom coordinated in a distorted tetra-hedral manner by two Cl(-) ligands and the terminal N atoms of two dimethyl N-cyano-dithio-imino-carbonate ligands. The two organic ligands are almost coplanar, with a dihedral angle of 5.99 (6)° between their least-squares planes. The crystal packing features pairs of inversion-related complexes that are held together through C-H⋯Cl and C-H⋯S inter-actions and π-π stacking [centroid-to-centroid distance = 3.515 (su?) Å]. Additional C-H⋯Cl and C-H⋯S inter-actions, as well as Cl⋯S contacts < 3.6 Å, consolidate the crystal packing. PMID:26870588

  4. In-vitro study on calcium carbonate crystal growth mediated by organic matrix extracted from fresh water pearls

    International Nuclear Information System (INIS)

    For the purpose of studying the mediation of organic matrix on the crystallization of calcium carbonate, water soluble matrix (WSM), acid soluble matrix (ASM) and acid insoluble matrix (AIM) were extracted from aragonite pearls and vaterite pearls respectively. Then, in-vitro calcium carbonate crystallization experiments under the control of these six organic matrices were carried out in the present study. Scanning electron microscopy (SEM) was utilized to observe the morphology of CaCO3 and Raman spectroscopy as a powerful technique was used to distinguish the crystal polymorph. Influences of the six kinds of organic matrices on the calcium carbonate crystal growth are proposed. ASM of vaterite pearls can induce vaterite to crystallize and WSM of aragonite pearls mediates to produce aragonite crystals. The single AIM membranes of the two pearls have no pronounced effect on the CaCO3 crystallization. Additionally, the crystal size obtained with the additive of WSM of the two kinds of pearls is smaller than that with the additive of ASM. Moreover, self-assembly phenomenon in the biomineralization process and the distorted morphology calcite are observed. Current results demonstrate important aspects of matrix protein-controlled crystallization, which is beneficial to the understanding of nacre biomineralization mechanism. Further study of the precise control of these matrix proteins on CaCO3 crystal growth is being processed. - Highlights: ► WSM, ASM and AIM are extracted from aragonite pearls and vaterite pearls. ► ASM of vaterite pearl induces vaterite. ► WSM of aragonite pearl mediates to produce aragonite. ► WSM can fine control crystal size smaller than that with the additive of ASM. ► Self-assembly and the distorted calcite existed in the mineralization process.

  5. Crystal structure of di-chlorido-bis-(dimethyl N-cyano-dithio-imino-carbonate)zinc.

    Science.gov (United States)

    Diop, Mouhamadou Birame; Diop, Libasse; Oliver, Allen G

    2016-03-01

    The Zn(II) atom in the title complex, [ZnCl2(C4H6N2S2)2], is coordinated in a distorted tetra-hedral manner by two Cl atoms and two terminal N atoms of two dimethyl N-cyano-dithio-imino-carbonate ligands. In the crystal, the complex mol-ecules are connected through C-H⋯Cl hydrogen bonds and Cl⋯S contacts, leading to a two-dimensional structure extending parallel to the ab plane. PMID:27006820

  6. Aboveground carbon in Quebec forests: stock quantification at the provincial scale and assessment of temperature, precipitation and edaphic properties effects on the potential stand-level stocking.

    Science.gov (United States)

    Duchesne, Louis; Houle, Daniel; Ouimet, Rock; Lambert, Marie-Claude; Logan, Travis

    2016-01-01

    Biological carbon sequestration by forest ecosystems plays an important role in the net balance of greenhouse gases, acting as a carbon sink for anthropogenic CO2 emissions. Nevertheless, relatively little is known about the abiotic environmental factors (including climate) that control carbon storage in temperate and boreal forests and consequently, about their potential response to climate changes. From a set of more than 94,000 forest inventory plots and a large set of spatial data on forest attributes interpreted from aerial photographs, we constructed a fine-resolution map (∼375 m) of the current carbon stock in aboveground live biomass in the 435,000 km(2) of managed forests in Quebec, Canada. Our analysis resulted in an area-weighted average aboveground carbon stock for productive forestland of 37.6 Mg ha(-1), which is lower than commonly reported values for similar environment. Models capable of predicting the influence of mean annual temperature, annual precipitation, and soil physical environment on maximum stand-level aboveground carbon stock (MSAC) were developed. These models were then used to project the future MSAC in response to climate change. Our results indicate that the MSAC was significantly related to both mean annual temperature and precipitation, or to the interaction of these variables, and suggest that Quebec's managed forests MSAC may increase by 20% by 2041-2070 in response to climate change. Along with changes in climate, the natural disturbance regime and forest management practices will nevertheless largely drive future carbon stock at the landscape scale. Overall, our results allow accurate accounting of carbon stock in aboveground live tree biomass of Quebec's forests, and provide a better understanding of possible feedbacks between climate change and carbon storage in temperate and boreal forests.

  7. Aboveground carbon in Quebec forests: stock quantification at the provincial scale and assessment of temperature, precipitation and edaphic properties effects on the potential stand-level stocking.

    Science.gov (United States)

    Duchesne, Louis; Houle, Daniel; Ouimet, Rock; Lambert, Marie-Claude; Logan, Travis

    2016-01-01

    Biological carbon sequestration by forest ecosystems plays an important role in the net balance of greenhouse gases, acting as a carbon sink for anthropogenic CO2 emissions. Nevertheless, relatively little is known about the abiotic environmental factors (including climate) that control carbon storage in temperate and boreal forests and consequently, about their potential response to climate changes. From a set of more than 94,000 forest inventory plots and a large set of spatial data on forest attributes interpreted from aerial photographs, we constructed a fine-resolution map (∼375 m) of the current carbon stock in aboveground live biomass in the 435,000 km(2) of managed forests in Quebec, Canada. Our analysis resulted in an area-weighted average aboveground carbon stock for productive forestland of 37.6 Mg ha(-1), which is lower than commonly reported values for similar environment. Models capable of predicting the influence of mean annual temperature, annual precipitation, and soil physical environment on maximum stand-level aboveground carbon stock (MSAC) were developed. These models were then used to project the future MSAC in response to climate change. Our results indicate that the MSAC was significantly related to both mean annual temperature and precipitation, or to the interaction of these variables, and suggest that Quebec's managed forests MSAC may increase by 20% by 2041-2070 in response to climate change. Along with changes in climate, the natural disturbance regime and forest management practices will nevertheless largely drive future carbon stock at the landscape scale. Overall, our results allow accurate accounting of carbon stock in aboveground live tree biomass of Quebec's forests, and provide a better understanding of possible feedbacks between climate change and carbon storage in temperate and boreal forests. PMID:26966680

  8. MODIFICATION OF PRECIPITATED CALCIUM CARBONATE FILLER USING SODIUM SILICATE/ZINC CHLORIDE BASED MODIFIERS TO IMPROVE ACID-RESISTANCE AND USE OF THE MODIFIED FILLER IN PAPERMAKING

    Directory of Open Access Journals (Sweden)

    Jing Shen

    2009-11-01

    Full Text Available In order to improve the acid-resistant property of papermaking grade precipitated calcium carbonate filler and to obtain modified filler in powder form, sodium silicate/zinc chloride based modifiers were used in filler modification, and the use of modified filler in papermaking of deinked pulp derived from recycled newspaper was also preliminarily investigated. Under the preliminarily optimized experimental conditions, when sodium silicate, zinc chloride, sodium hexametaphosphate, and phosphoric acid with dosages of 10 wt%, 3 wt%, 1 wt% and 0.2 wt%, respectively, were used as modifiers, and when the temperature, aging time, and PCC concentration during the filler modification process was 70 oC, 7 h and 9.1 wt%, respectively, the acid-resistant property of filler was significantly improved after modification, as evaluated using alum consumption and pH methods. The use of modified precipitated calcium carbonate filler prepared under the optimized conditions provided considerably more brightness and light scattering improvement in comparison to unmodified filler, and filler modification was found to have only negligible influence on tensile and burst strength of the paper, air permeability of the paper, and retention performance of the filler. Surface analysis of the modified filler using XPS and SEM confirmed the occurring of surface encapsulation and modification of precipitated calcium carbonate filler when the relevant modifiers were used in filler modification. The encapsulating effect of modifiers on filler was thought to be favorable to improvement in acid-resistant property, and optical properties of the filled paper.

  9. A comparative investigation on strain induced crystallization for graphene and carbon nanotubes filled natural rubber composites

    Directory of Open Access Journals (Sweden)

    D. H. Fu

    2015-07-01

    Full Text Available Natural rubber containing graphene and carbon nanotubes (CNTs composites were prepared by ultrasonicallyassisted latex mixing. Natural rubber filled by both graphene and CNTs show significant enhanced tensile strength, while graphene exhibits a better reinforcing effect than CNTs. Strain-induced crystallization in natural rubber composites during stretching was determined by synchrotron wide-angle X-ray diffraction. With the addition of CNTs or graphene, the crystallization for natural rubber occurs at a lower strain compared to unfilled natural rubber, and the strain amplification effects were observed. The incorporation of graphene results in a faster strain-induced crystallization rate and a higher crystallinity compared to CNTs. The entanglement-bound rubber tube model was used to analyze the chain network structure and determine the network parameters of composites. The results show that the addition of graphene or CNTs has an influence on the molecular network structure and improves the contribution of entanglement to the conformational constraint, while graphene has a more marked effect than CNTs.

  10. Electrochemical quartz crystal microbalance measurement of a Li4Ti5O12 composite electrode in a carbonate electrolyte

    Science.gov (United States)

    Serizawa, Nobuyuki; Shono, Kumi; Kobayashi, Yo; Miyashiro, Hajime; Katayama, Yasushi; Miura, Takashi

    2015-11-01

    Electrochemical quartz crystal microbalance (EQCM) measurement is conducted with a Li4Ti5O12 (lithium titanium oxide, LTO)-coated quartz crystal electrode in a carbonate electrolyte (ethylene carbonate + dimethyl carbonate; 50: 50 vol%) containing 1 M LiPF6. In-situ monitoring of the mass change during the charge and discharge of the LTO electrode can be achieved quantitatively because of the "zero-strain" property of LTO with Li+ insertion and the probably low reactivity between LTO and the electrolyte. The local changes of viscosity and density of the electrolyte contacting the LTO electrode are detected via the resonance resistance of the quartz crystal electrode, suggesting the local concentrations of Li+ and counter anion changed significantly during insertion and extraction of Li+ in the organic electrolyte.

  11. Low temperature crystallization of diamond-like carbon films to graphene

    Energy Technology Data Exchange (ETDEWEB)

    Tinchev, Savcho, E-mail: stinchev@ie.bas.bg [Institute of Electronics, Bulgarian Academy of Sciences, Tzarigradsko Chaussee 72, 1784 Sofia (Bulgaria); Valcheva, Evgenia [Physics Department, Sofia University, J. Bourchier 5, 1164 Sofia (Bulgaria); Petrova, Elitza [Institute of Electronics, Bulgarian Academy of Sciences, Tzarigradsko Chaussee 72, 1784 Sofia (Bulgaria)

    2013-09-01

    Plasma surface modification was used to fabricate graphene on the top of insulating diamond-like carbon films. It is shown that by a combination of pulsed argon plasma treatment and thermal annealing at 350{sup o}C it is possible to achieve crystallization of amorphous carbon to graphene. The observed Raman spectra are typical for defected graphene-splitted D- and G-peaks and a broad 2D-peak. Because interpretation of Raman spectra of such complicated system is not easy we have calculated Raman signals of graphene on an amorphous hydrogenated carbon film deposited on a Si substrate. Our simulation results show that multiple reflections and interference effects lead to enhancement of Raman signal of the system. The characteristic for graphene G and 2D bands reach maximal enhancement for thicknesses of the amorphous hydrogenated carbon film of about 75 nm and 230 nm. We estimate that the interference enhancement of the 2D graphene Raman signal is very weak in contrast to that of the G band signal simulated for the underlying diamond-like carbon films on silicon substrate only. Therefore experimentally measured Raman spectra of the whole graphene/a-C:H/Si system probably will consist of interference enhanced but still weak 2D graphene peak and stronger D and G peaks dominated by G and D Raman bands of the a-C:H. This conclusion is in line with observed experimental Raman spectra. Electrical field effect measurements of the samples show ambipolar dependence, typical for single-layer graphene.

  12. Influence of airflow rate and substrate nature on heterogeneous struvite precipitation.

    Science.gov (United States)

    Saidou, H; Ben Moussa, S; Ben Amor, M

    2009-01-01

    In wastewater treatment plants a hard scale consisting of struvite crystals can be formed, in pipes and recirculation pumps, during anaerobic digestion of wastewater. This study was conducted to evaluate the effect of airflow rate and substrate nature on nucleation type, induction period and supersaturation coefficient during struvite precipitation. A crystallization reactor similar to that designed for calcium carbonate precipitation was used. The pH of synthetic wastewater solution was increased by air bubbling. Experimental results indicated that the airflow increased heterogeneous precipitation of struvite. The susceptibility to scale formation was more important on polyamide and polyvinyl chloride than on stainless steel. In all cases, X-ray diffraction and infrared spectroscopy showed that the precipitated solid phase was solely struvite. No difference in crystal morphology was observed. However, at similar experimental conditions, the particle size of struvite was higher for stainless-steel material than that for plastic materials. PMID:19213469

  13. On the complex conductivity signatures of calcite precipitation

    Energy Technology Data Exchange (ETDEWEB)

    Wu, Yuxin; Hubbard, Susan; Williams, Kenneth Hurst; Ajo-Franklin, Jonathan

    2009-11-01

    Calcite is a mineral phase that frequently precipitates during subsurface remediation or geotechnical engineering processes. This precipitation can lead to changes in the overall behavior of the system, such as flow alternation and soil strengthening. Because induced calcite precipitation is typically quite variable in space and time, monitoring its distribution in the subsurface is a challenge. In this research, we conducted a laboratory column experiment to investigate the potential of complex conductivity as a mean to remotely monitor calcite precipitation. Calcite precipitation was induced in a glass bead (3 mm) packed column through abiotic mixing of CaCl{sub 2} and Na{sub 2}CO{sub 3} solutions. The experiment continued for 12 days with a constant precipitation rate of {approx}0.6 milimole/d. Visual observations and scanning electron microscopy imaging revealed two distinct phases of precipitation: an earlier phase dominated by well distributed, discrete precipitates and a later phase characterized by localized precipitate aggregation and associated pore clogging. Complex conductivity measurements exhibited polarization signals that were characteristic of both phases of calcite precipitation, with the precipitation volume and crystal size controlling the overall polarization magnitude and relaxation time constant. We attribute the observed responses to polarization at the electrical double layer surrounding calcite crystals. Our experiment illustrates the potential of electrical methods for characterizing the distribution and aggregation state of nonconductive minerals like calcite. Advancing our ability to quantify geochemical transformations using such noninvasive methods is expected to facilitate our understanding of complex processes associated with natural subsurface systems as well as processes induced through engineered treatments (such as environmental remediation and carbon sequestration).

  14. Influence of magnetic field on the morphology of the andrographolide crystal from supercritical carbon dioxide extraction crystallization

    Science.gov (United States)

    Chen, Kexun; Zhang, Xingyuan; Pan, Jian; Zhang, Wencheng; Yong, Ji; Yin, Wenhong

    2003-10-01

    In this paper, a supercritical fluid extraction-crystallization of andrographolide, a kind of Chinese traditional medicine, was investigated. We have studied the extraction-crystallization process with or without magnet in the extractor, respectively. It was found that the presence of magnetic field is an important factor influencing the quality of the products. SEM images showed that the crystal was slice-like in shape, and many slices reunited together in the absence of magnet. Further research showed that pressure had a certain effect on the morphology of the crystal.

  15. Carbon and hydrogen isotope composition of plant biomarkers from lake sediments as proxies for precipitation changes across Heinrich Events in the subtropics

    Science.gov (United States)

    Arnold, T. E.; Diefendorf, A. F.; Brenner, M.; Freeman, K. H.; Curtis, J. H.

    2015-12-01

    Lake Tulane is a relatively deep (~23 m) solution lake in south-central Florida. Its depth and location on a structural high, the Lake Wales Ridge, enabled continuous lacustrine sediment accumulation over the past >60,000 years. Pollen in the lake sediments indicate repeated major shifts in the vegetation community, with six peaks in Pinus (pine) abundance that coincide with the most intense cold phases of Dansgaard-Oeschger cycles and the Heinrich events that terminate them. Alternating with Pinus peaks are zones with high relative percentages of Quercus (oak), Ambrosia (ragweed), Lyonia (staggerbush) and Ceratiola (rosemary) pollen, genera that today occupy the most xeric sites on the Florida landscape. This suggests the pollen record indicates the Pinus phases, and therefore Heinrich Events, were wetter than the intervening Quercus phases. To test the connection between Heinrich Events and precipitation in Florida, we analyzed the carbon (δ13C) and hydrogen (δD) isotope signatures of plant biomarkers extracted from the Lake Tulane sediment core as proxies of paleohydrology. The δ13C of plant biomarkers, such as n-alkanes and terpenoids, are determined, in part, by changes in water-use efficiency (WUE = Assimilation/Transpiration) in plant communities, which changes in response to shifts in mean annual precipitation. Plant δ13C values can, therefore, provide a rough indication of precipitation changes when other factors, such as plant community, are relatively stable throughout time. Paleohydrology is also recorded in the δD of plant leaf waxes, which are strongly controlled by precipitation δD. In this region, precipitation δD is negatively correlated with rainfall amount (i.e. the "amount" effect) and positively correlated with aridity. Thus, the δ13C and δD signatures of molecular plant biomarkers provide relative indicators of precipitation change, and when combined, provide a test of our hypothesis that vegetation changes in this region are driven

  16. Effect of hot rolling temperature on grain size and precipitation hardening in a Ti-microalloyed low-carbon martensitic steel

    International Nuclear Information System (INIS)

    Highlights: ► TiC precipitation can induce the grain refinement after reheating quenching. ► TiC in steel rolled at 950 °C is more and finer. ► The grain size of steel rolled at 950 °C and followed reheating is much finer. ► The strength of steel rolled at 950 °C is much higher. - Abstract: The grain refinement and strength improvement resulted from hot rolling temperature in Ti microalloyed low carbon martensitic steel was investigated in this study. Two different started hot rolling temperatures (950 °C and 1100 °C) but with the same reheating quenching process were applied to the steel. The microstructures and second precipitated particles were examined by scanning electron microscopy (SEM), electron back-scattered diffraction (EBSD), transmission electron microscopy (TEM), high resolution transmission electron microscopy (HRTEM), X-rays diffraction and phase analysis method. It was found that hot rolling could induce the precipitation of TiC. Moreover, the amount of the TiC in steel rolled at 950 °C is higher and the size of the precipitates is much finer than that in steel rolled at 1100 °C. Both the large deformation without recrystallization and the precipitates in steel rolled at 950 °C are more effective on the grain refinement after the reheating process, in which the effective grain size (EGS) can be refined to 1.4 μm. In addition, the steel rolled at 950 °C exhibits a much higher strength than that rolled at 1100 °C due to the additional dislocation strengthening and more precipitation strengthening

  17. Effects of pore-scale precipitation on permeability and flow

    Science.gov (United States)

    Noiriel, Catherine; Steefel, Carl I.; Yang, Li; Bernard, Dominique

    2016-09-01

    The effects of calcite precipitation on porous media permeability and flow were evaluated with a combined experimental and modeling approach. X-ray microtomography images of two columns packed with glass beads and calcite (spar crystals) or aragonite (Bahamas ooids) injected with a supersaturated solution (log Ω = 1.42) were processed in order to calculate rates of calcite precipitation with a spatial resolution of 4.46 μm. Identification and localization of the newly precipitated crystals on the 3D images was performed and results used to calculate the crystal growth rates and velocities. The effects of carbonate precipitation were also evaluated in terms of the integrated precipitation rate over the length of the column, crystal shape, surface area and pore roughness changes. While growth was epitaxial on calcite spar, calcite rhombohedra formed on glass beads and clusters of polyhedrons formed on aragonite ooids. Near the column inlet, calcite precipitation occurred preferentially on carbonate grains compared to glass beads, with almost 100% of calcite spar surface area covered by new crystals versus 92% in the case of aragonite and 11% in the case of glass beads. Although the experimental chemistry and flow boundary conditions in the two columns were similar, their porosity-permeability evolution was different because the nucleation and subsequent crystal growth on the two substrates (i.e., calcite spar and aragonite ooids) was very different. The impact of mineral precipitation on pore-scale flow and permeability was evaluated using a pore-scale Stokes solver that accounted for the changes in pore geometry. For similar magnitude reductions in porosity, the decrease in permeability was highest within the sample that experienced the greatest increase in pore roughness. Various porous media models were generated to show the impact of different crystal growth patterns and pore roughness changes on flow and permeability-porosity relationship. Under constant flow

  18. Pore-scale simulation of calcium carbonate precipitation and dissolution under highly supersaturated conditions in a microfludic pore network

    Science.gov (United States)

    Yoon, H.; Dewers, T. A.; Valocchi, A. J.; Werth, C. J.

    2011-12-01

    Dissolved CO2 during geological CO2 storage may react with minerals in fractured rocks or confined aquifers and cause mineral precipitation. The overall rate of reaction can be affected by coupled processes among hydrodynamics, transport, and reactions at pore-scale. Pore-scale models of coupled fluid flow, reactive transport, and CaCO3 precipitation and dissolution are applied to account for transient experimental results of CaCO3 precipitation and dissolution under highly supersaturated conditions in a microfluidic pore network (i.e., micromodel). Pore-scale experiments in the micromodel are used as a basis for understanding coupled physics of systems perturbed by geological CO2 injection. In the micromodel, precipitation is induced by transverse mixing along the centerline in pore bodies. Overall, the pore-scale model qualitatively captured the governing physics of reactions such as precipitate morphology, precipitation rate, and maximum precipitation area in first few pore spaces. In particular, we found that proper estimation of the effective diffusion coefficient and the reactive surface area is necessary to adequately simulate precipitation and dissolution rates. As the model domain increases, the effect of flow patterns affected by precipitation on the overall reaction rate also increases. The model is also applied to account for the effect of different reaction rate laws on mineral precipitation and dissolution at pore-scale. Reaction rate laws tested include the linear rate law, nonlinear power law, and newly-developed rate law based on in-situ measurements at nano scale in the literature. Progress on novel methods for upscaling pore-scale models for reactive transport are discussed, and are being applied to mineral precipitation patterns observed in natural analogues. H.Y. and T. D. were supported as part of the Center for Frontiers of Subsurface Energy Security, an Energy Frontier Research Center funded by the U.S. Department of Energy, Office of

  19. Detailed crystallization study of co-precipitated Y1.47 Gd1.53 Fe5 O12 and relevant magnetic properties

    International Nuclear Information System (INIS)

    The crystallization process of co-precipitated Y1.5Gd1.5Fe5O12 powder heated up to 1000 deg C at rate of 5 deg C min-1 was investigated. Above 810 deg C crystalline Y1.47Gd1.53Fe5O12 was obtained with a lattice parameter of 12.41 A and a theoretical density of 5.84 g cm-3. Dry pressed rings were sintered at 1270 and 1320 deg C, increasing the grain-size from 3.1 to 6.5 μm, the theoretical density by 87.6 to 95.3% and decreasing Hc from 2.9725 to 1.4005 Oe. Additionally, Hc increased when the frequency of the hysteresis graph varied from 60 Hz to 10 kHz, the curie temperature was 282.4 deg C and Ms equalled 9.25 emu g-1 (0.17 kG) agreeing well with the Bs-value of the hysteresis graph and literature values. (author)

  20. Solubility dynamic of methyl yellow and carbon black in microemulsions and lamellar liquid crystal of water, non ionic surfactants and cyclohexane system

    Science.gov (United States)

    Amran, A.; Harfianto, R.; Dewi, W. Y.; Beri, D.; Putra, A.

    2016-02-01

    Solubility dynamics of methyl yellow and carbon black in microemulsions and liquid crystals of water, non-ionic surfactants and cyclohexane system, have been investigated. Actually, solubility dynamics of these dyes both in microemulsion (w/o microemulsions) and the lamellar liquid crystal (LLC) were strongly related to the chemical composition, nature and characteristics of microemulsions and the lamellar liquid crystals.

  1. Precipitated calcium carbonate (PCC - cellulose composite fillers: Effects of PCC particle structure on the production and properties of uncoated fine paper

    Directory of Open Access Journals (Sweden)

    Paulapuro, H.

    2007-02-01

    Full Text Available This work examines the precipitation of PCC – pulp composite fillers with varying crystal habits and their effects on the papermaking properties of printing and writing paper. Colloidal (c-PCC, rhombohedral (r-PCC, and scalenohedral types (s-PCC of composite PCCs were produced and compared with commercial reference PCCs. Scanning electron micros-copy showed the c-PCC to be a high-surface-area nano-structured PCC. The rhombohedral composite was formed in clusters like a spider-web structure. Under similar experimental conditions, composite PCC was formed as individual ellipsoidal crystals and some of the particles had malformed structure, in contrast to the structured reference s-PCC. The co-precipitation and the structure of PCC significantly influence the forming, consolidation, and properties of paper, as well as its perform-ance in printing.Composite c-PCC showed the highest retention during forming. At higher filler contents, dewatering was reduced significantly with handsheets containing s- and r-PCC composite fillers. Colloidal composite hand-sheets showed the lowest tensile index and internal bond strength, while the rhombohedral composite gave the highest z-directional bond strength. Compared with the traditional reference samples containing commercial PCCs, paper with s- and r-composites had significantly higher density but similar light scattering ability. Addition of fibrillar fines to fine paper increased print rub fastness significantly in both laser and inkjet printed samples.

  2. Modelling a nonlinear optical switching in a standard photonic crystal fiber infiltrated with carbon disulfide

    Science.gov (United States)

    Munera, Natalia; Acuna Herrera, Rodrigo

    2016-06-01

    In this letter, a numerical analysis is developed for the propagation of ultrafast optical pulses through a standard photonic crystal fiber (PCF) consisting of two infiltrated holes using carbon disulfide (CS2). This material is a good choice since it has highly nonlinear properties, what makes it a good candidate for optical switching and broadband source at low power compared to traditional nonlinear fiber coupler. Based on supermodes theory, a set of generalized nonlinear equations is presented in order to study the propagation characteristics. It is shown in this letter that it is possible to get optical switching behavior at low power and how the dispersion, as well as, the two infiltrated holes separation influence this effect. Finally, we see that supercontinuum generation can be induced equally in both infiltrated holes despite no initial excitation at one hole.

  3. Light-melt adhesive based on dynamic carbon frameworks in a columnar liquid-crystal phase

    Science.gov (United States)

    Saito, Shohei; Nobusue, Shunpei; Tsuzaka, Eri; Yuan, Chunxue; Mori, Chigusa; Hara, Mitsuo; Seki, Takahiro; Camacho, Cristopher; Irle, Stephan; Yamaguchi, Shigehiro

    2016-07-01

    Liquid crystal (LC) provides a suitable platform to exploit structural motions of molecules in a condensed phase. Amplification of the structural changes enables a variety of technologies not only in LC displays but also in other applications. Until very recently, however, a practical use of LCs for removable adhesives has not been explored, although a spontaneous disorganization of LC materials can be easily triggered by light-induced isomerization of photoactive components. The difficulty of such application derives from the requirements for simultaneous implementation of sufficient bonding strength and its rapid disappearance by photoirradiation. Here we report a dynamic molecular LC material that meets these requirements. Columnar-stacked V-shaped carbon frameworks display sufficient bonding strength even during heating conditions, while its bonding ability is immediately lost by a light-induced self-melting function. The light-melt adhesive is reusable and its fluorescence colour reversibly changes during the cycle, visualizing the bonding/nonbonding phases of the adhesive.

  4. Two-step electrical percolation in nematic liquid crystals filled with multiwalled carbon nanotubes

    Science.gov (United States)

    Tomylko, Serhiy; Yaroshchuk, Oleg; Lebovka, Nikolai

    2015-07-01

    Percolation of carbon nanotubes (CNTs) in liquid crystals (LCs) opens the way for a unique class of anisotropic hybrid materials with a complex dielectric constant widely controlled by CNT concentration. Percolation in such systems is commonly described as a one-step process starting at a very low loading of CNTs. In the present study the two-step percolation was observed in the samples of thickness 250 μ m obtained by pressing the suspension between two substrates. The first threshold concentration, Cnp1˜10-4 wt.%, was sensitive to temperature and phase state of LC, while the second one, Cnp2˜10-1 wt.%, remained practically unchanged in the temperature tests. The two-stage nature of percolation was explained on a base of mean-field theory assuming core-shell structure of CNTs.

  5. Isothermal Crystallization of Poly(L-lactide) Induced by Graphene Nanosheets and Carbon Nanotubes: A Comparative Study

    Energy Technology Data Exchange (ETDEWEB)

    Xu, J.; Chen, T; Yang, C; Li, Z; Mao, Y; Zeng, B; Hsiao, B

    2010-01-01

    Low-dimensional nanoparticles have a strong ability to induce the crystallization of polymer matrices. One-dimensional carbon nanotubes (CNTs) and two-dimensional graphene nanosheets (GNSs), both of which are both carbon-based nanoparticles, provide a good opportunity to investigate the effects of differently dimensional nanoparticles on the crystallization behavior of a polymer. For this purpose, respective nanocomposites of CNTs and GNSs with poly(L-lactide) (PLLA) as matrix were prepared by solution coagulation. Time-resolved Fourier-transform infrared spectroscopy (FTIR) and synchrotron wide-angle X-ray diffraction (WAXD) were performed to probe chain conformational changes and to determine the crystallization kinetics during the isothermal crystallization of the PLLA nanocomposites and neat PLLA, especially in the early stages. Both CNTs and GNSs could serve as nucleating agents in accelerating the crystallization kinetics of PLLA; however, the ability of CNTs to induce crystallization was stronger than that of GNSs. On increasing the content of CNTs from 0.05 to 0.1 wt %, the induction period was shortened and the crystallization rate was enhanced, but the reverse situation was found for GNSs nanocomposites. In the case of neat PLLA, -CH{sub 3} interchain interactions preceded -(COC + CH{sub 3}) interchain interactions during the crystallization. Conversely, in the CNTs and GNSs nanocomposites, the conformational ordering began with -(COC + CH{sub 3}) interchain interactions, which resulted directly in a reduced induction period. Interchain interactions of this type could be explained in terms of surface-induced conformational order (SICO). Finally, the effect of the dimensionality of the nanoparticles on the crystallization behavior of PLLA is discussed.

  6. Diamond crystallization in a CO2-rich alkaline carbonate melt with a nitrogen additive

    Science.gov (United States)

    Khokhryakov, Alexander F.; Palyanov, Yuri N.; Kupriyanov, Igor N.; Nechaev, Denis V.

    2016-09-01

    Diamond crystallization was experimentally studied in a CO2-bearing alkaline carbonate melt with an increased content of nitrogen at pressure of 6.3 GPa and temperature of 1500 °C. The growth rate, morphology, internal structure of overgrown layers, and defect-impurity composition of newly formed diamond were investigated. The type of growth patterns on faces, internal structure, and nitrogen content were found to be controlled by both the crystallographic orientation of the growth surfaces and the structure of the original faces of diamond seed crystals. An overgrown layer has a uniform structure on the {100} plane faces of synthetic diamond and a fibrillar (fibrous) structure on the faceted surfaces of a natural diamond cube. The {111} faces have a polycentric vicinal relief with numerous twin intergrowths and micro twin lamellae. The stable form of diamond growth under experimental conditions is a curved-face hexoctahedron with small cube faces. The nitrogen impurity concentration in overgrown layers varies depending on the growth direction and surface type, from 100 to 1100 ppm.

  7. Variations in soil carbon sequestration and their determinants along a precipitation gradient in seasonally dry tropical forest ecosystems.

    Science.gov (United States)

    Campo, Julio; Merino, Agustín

    2016-05-01

    The effect of precipitation regime on the C cycle of tropical forests is poorly understood, despite the existence of models that suggest a drier climate may substantially alter the source-sink function of these ecosystems. Along a precipitation regime gradient containing 12 mature seasonally dry tropical forests growing under otherwise similar conditions (similar annual temperature, rainfall seasonality, and geological substrate), we analyzed the influence of variation in annual precipitation (1240 to 642 mm) and duration of seasonal drought on soil C. We investigated litterfall, decomposition in the forest floor, and C storage in the mineral soil, and analyzed the dependence of these processes and pools on precipitation. Litterfall decreased slightly - about 10% - from stands with 1240 mm yr(-1) to those with 642 mm yr(-1) , while the decomposition decreased by 56%. Reduced precipitation strongly affected C storage and basal respiration in the mineral soil. Higher soil C storage at the drier sites was also related to the higher chemical recalcitrance of litter (fine roots and forest floor) and the presence of charcoal across sites, suggesting an important indirect influence of climate on C sequestration. Basal respiration was controlled by the amount of recalcitrant organic matter in the mineral soil. We conclude that in these forest ecosystems, the long-term consequences of decreased precipitation would be an increase in organic layer and mineral soil C storage, mainly due to lower decomposition and higher chemical recalcitrance of organic matter, resulting from changes in litter composition and, likely also, wildfire patterns. This could turn these seasonally dry tropical forests into significant soil C sinks under the predicted longer drought periods if primary productivity is maintained. PMID:26913708

  8. Microstructural record of cataclastic and dissolution-precipitation processes from shallow crustal carbonate strike-slip faults, Northern Calcareous Alps (Austria)

    Science.gov (United States)

    Bauer, Helene; Grasemann, Bernhard; Decker, Kurt

    2015-04-01

    The concept of coseismic slip and aseismic creep deformation along faults is supported by the variability of natural fault rocks and their microstructures. Faults in carbonate rocks are characterized by very narrow principal slip zones (cm to mm wide) containing (ultra)cataclastic fault rocks that accommodate most of the fault displacement. Fluidization of ultracataclastic sub layers and thermal decomposition of calcite due to frictional heating have been proposed as possible indicators for seismic slip. Dissolution-precipitation (DP) processes are possible mechanism of aseismic sliding, resulting in spaced cleavage solution planes and associated veins, indicating diffusive mass transfer and precipitation in pervasive vein networks. We investigated exhumed, sinistral strike-slip faults in carbonates of the Northern Calcareous Alps. The study presents microstructural investigations of natural carbonate fault rocks that formed by cataclastic and dissolution-precipitation related deformation processes. Faults belong to the eastern segment of the Salzachtal-Ennstal-Mariazell-Puchberg (SEMP) fault system that was formed during eastward lateral extrusion of the Eastern Alps in Oligocene to Lower Miocene. The investigated faults accommodated sinistral slip between several tens and few hundreds of meters. Microstructural analysis of fault rocks was done with scanning electron microscopy and optical microscopy. Deformation experiments of natural fault rocks are planned to be conducted at the Sapienza University of Roma and should be available at the meeting. The investigated fault rocks give record of alternating cataclastic deformation and DP creep. DP fault rocks reveal various stages of evolution including early stylolites, pervasive pressure solution seams and cleavage, localized shear zones with syn-kinematic calcite fibre growth and mixed DP/cataclastic microstructures, involving pseudo sc- and scc'-fabrics. Pressure solution seams host fine grained kaolinit, chlorite

  9. Spatial variability in photosynthetic and heterotrophic activity drives localized δ13C org fluctuations and carbonate precipitation in hypersaline microbial mats.

    Science.gov (United States)

    Houghton, J; Fike, D; Druschel, G; Orphan, V; Hoehler, T M; Des Marais, D J

    2014-11-01

    Modern laminated photosynthetic microbial mats are ideal environments to study how microbial activity creates and modifies carbon and sulfur isotopic signatures prior to lithification. Laminated microbial mats from a hypersaline lagoon (Guerrero Negro, Baja California, Mexico) maintained in a flume in a greenhouse at NASA Ames Research Center were sampled for δ(13) C of organic material and carbonate to assess the impact of carbon fixation (e.g., photosynthesis) and decomposition (e.g., bacterial respiration) on δ(13) C signatures. In the photic zone, the δ(13) C org signature records a complex relationship between the activities of cyanobacteria under variable conditions of CO2 limitation with a significant contribution from green sulfur bacteria using the reductive TCA cycle for carbon fixation. Carbonate is present in some layers of the mat, associated with high concentrations of bacteriochlorophyll e (characteristic of green sulfur bacteria) and exhibits δ(13) C signatures similar to DIC in the overlying water column (-2.0‰), with small but variable decreases consistent with localized heterotrophic activity from sulfate-reducing bacteria (SRB). Model results indicate respiration rates in the upper 12 mm of the mat alter in situ pH and HCO3- concentrations to create both phototrophic CO2 limitation and carbonate supersaturation, leading to local precipitation of carbonate minerals. The measured activity of SRB with depth suggests they variably contribute to decomposition in the mat dependent on organic substrate concentrations. Millimeter-scale variability in the δ(13) C org signature beneath the photic zone in the mat is a result of shifting dominance between cyanobacteria and green sulfur bacteria with the aggregate signature overprinted by heterotrophic reworking by SRB and methanogens. These observations highlight the impact of sedimentary microbial processes on δ(13) C org signatures; these processes need to be considered when attempting to relate

  10. Polypropylene/Graphene and Polypropylene/Carbon Fiber Conductive Composites: Mechanical, Crystallization and Electromagnetic Properties

    Directory of Open Access Journals (Sweden)

    Chien-Lin Huang

    2015-11-01

    Full Text Available This study aims to examine the properties of composites that different carbon materials with different measurements can reinforce. Using a melt compounding method, this study combines polypropylene (PP and graphene nano-sheets (GNs or carbon fiber (CF to make PP/GNs and PP/CF conductive composites, respectively. The DSC results and optical microscopic observation show that both GNs and CF enable PP to crystalize at a high temperature. The tensile modulus of PP/GNs and PP/CF conductive composites remarkably increases as a result of the increasing content of conductive fillers. The tensile strength of the PP/GNs conductive composites is inversely proportional to the loading level of GNs. Containing 20 wt% of GNs, the PP/GNs conductive composites have an optimal conductivity of 0.36 S/m and an optimal EMI SE of 13 dB. PP/CF conductive composites have an optimal conductivity of 10−6 S/m when composed of no less than 3 wt% of CF, and an optimal EMI SE of 25 dB when composed of 20 wt% of CF.

  11. Kinetics of Glass Transition and Crystallization in Carbon Nanotube Reinforced Mg-Cu-Gd Bulk Metallic Glass

    Institute of Scientific and Technical Information of China (English)

    2006-01-01

    Mg65Cu25Gd10 bulk metallic glass and its carbon nanotube reinforced composite were prepared. Differential scanning calorimeter (DSC) was used to investigate the kinetics of glass transition and crystallization processes. The influence of CNTs addition to the glass matrix on the glass transition and crystallization kinetics was studied. It is shown that the kinetic effect on glass transition and crystallization are preserved for both the monothetic glass and its glass composite.Adding CNTs in to the glass matrix reduces the influence of the heating rate on the crystallization process. In addition, the CNTs increase the energetic barrier for the glass transition. This results in the decrease of GFA. The mechanism of the GFA decrease was also discussed.

  12. The crystal chemistry and the compressibility of silicate-carbonate minerals:Spurrite, galuskinite and tilleyite

    Institute of Scientific and Technical Information of China (English)

    Jing Gao; Xiang Wu; Shan Qin

    2015-01-01

    Spurrite Ca5(SiO4)2(CO3), galuskinite Ca7(SiO4)3(CO3) and tilleyite Ca5(Si2O7)(CO3)2 are three representa-tive minerals formed in high-temperature skarns in the silicate-carbonate system. Their crystal chemistry and compressibility have been investigated using first-principles theoretical simulation. These minerals are structurally described as the combination of interwoven layers constituted by Ca polyhedra and Si polyhedra, with the [CO3] triangles being“separators”to depolymerize the SieCa aggregations. With the effect of pressure, the Si polyhedra and the [CO3] groups present rigid behaviors whereas the CaeO bonds undergo considerable compression. Several pressure-induced abnormities in the lattice parameter vari-ations have been identified, revealing the existence of subtle changes in the compression process. Isothermal equations of state parameters are obtained:K0 ¼ 71.1(1) GPa, V0 ¼ 1003.31(4) Å3 and K00 ¼ 5.4(1) for spurrite; K0 ¼ 75.0(1) GPa, V0 ¼ 1360.30(7) Å3, K00 ¼ 5.4(1) for galuskinite, and K0 ¼ 69.7(3) GPa, V0 ¼ 1168.90(2) Å3 and K00 ¼ 4.0(1) for tilleyite. These compounds have similar K0 values to calcite CaCO3 but are much more compressible than larnite b-Ca2SiO4. Generally for these minerals, the bulk modulus exhibits a negative correlation with the [CO3] proportion. The structural and compressional properties of silicate-carbonate minerals compared with silicates and carbonates are expected to be a guide for further investigations on Si polyhedra and [CO3] coexistent phases.

  13. Study on the crystal morphology and melting behavior of isothermally crystallized composites of short carbon fiber and poly(trimethylene terephthalate)

    Institute of Scientific and Technical Information of China (English)

    Mingtao RUN; Hongzan SONG; Yanping HAO

    2009-01-01

    The spherulites of the short carbon fibcr(SCF)/ poly (trimethylcne terephthalate) (PTT) composites forrned in limited space at designed temperatures, and their melting behaviors were studied by the polarized optical microscopy, atomic force microscopy (AFM), and scanning electron microscopy (SEM), respectively. The results suggest that SCF content, isothermal crystallization temperatures, and the film thicknesses influence the crystal morphology of the composites. The dimension of the spherulites is decreased with increasing SCF content, but whether banded or nonbandcd spherulites will form in the composites is not depondcnt on SCF content However, the crystal morphology of the composites depends strongly on the temperature. When the isothermal crystallization temperatures increase from 180℃ to 230℃, the crystal morphology of SCF/PTT composites continuously changes in the following order: nonbanded → banded → nonbanded spherulites. Disconti-nuous circle lines form in the film when the film thickness increases from 30 to 60 μm. Basing on the SEM observation, it is found that these circle lines are cracks formed due to the constriction difference of the different parts of the sphemlites. These cracks are formed when the film is cooled from the isothermal crystallization temperature to the room tempera-ture at a slow cooling rate; while they will disappear gradually at different temperatures in the heating process. The crack will appear/disappear first around the center of the spherulite when the film was cooled/heated. The nontwisted or slightly twisted lamellas will reorganize to form highly twisted lamellas inducing apparent banded texture of the sphemlites.

  14. Mesoporous MEL, BEA, and FAU zeolite crystals obtained by in situ formation of carbon template over metal nanoparticles

    DEFF Research Database (Denmark)

    Abildstrøm, Jacob Oskar; Ali, Zahra Nasrudin; Mentzel, Uffe Vie;

    2016-01-01

    Here, we report the synthesis and characterization of hierarchical zeolite materials with MEL, BEA and FAU structures. The synthesis is based on the carbon templating method with an in situ-generated carbon template. Through the decomposition of methane and deposition of coke over nickel nanopart......Here, we report the synthesis and characterization of hierarchical zeolite materials with MEL, BEA and FAU structures. The synthesis is based on the carbon templating method with an in situ-generated carbon template. Through the decomposition of methane and deposition of coke over nickel...... nanoparticles supported on silica, a carbon–silica composite is obtained and exploited as a combined carbon template/silica source for the zeolite synthesis. The mesoporous zeolite materials were all prepared by hydrothermal crystallization in alkaline media followed by removal of the carbon template...... by combustion, which results in zeolite single crystals with intracrystalline pore volumes of up to 0.44 cm3 g−1. The prepared zeolite structures are characterized by XRD, SEM, TEM and N2 physisorption measurements. ....

  15. Alfalfa carbon and nitrogen sequestration patterns and effects of temperature and precipitation in three agro-pastoral ecotones of northern China.

    Directory of Open Access Journals (Sweden)

    Shujuan Chang

    Full Text Available Alfalfa (Medicago sativa L. is a primary and widely cultivated forage crop in China. As a perennial leguminous grass, continuous planted alfalfa may influence carbon and nitrogen sequestration in soils. We evaluated the effect of alfalfa, planted for different lengths of time, and temperature and precipitation on soil organic carbon (SOC and total nitrogen (TN contents, and estimated soil SOC and TN inventories from 0-60 cm in three agro-pastoral ecotones of northern China. Alfalfa SOC and TN storage patterns were significantly different with increasing soil depths between the three regions of northern China. Continuous alfalfa grassland planted had a positive effect on accumulation of both SOC and TN in the Northwest region, whereas SOC storage peaked 6-7 years after planting in the Northeast and North region. Moreover, relatively higher TN storage appeared 7 years after planting in the Northeast and North regions. This study controlled as many factors as possible, but we caution that such temporal inferences could be artifacts of site selection. The regression analysis indicated that SOC and TN accumulation was mainly dependent on temperature (≥10°C of effective total accumulated temperature in the North region. Precipitation in the growing season was the main limiting factor for SOC storage in the Northwest region and TN accumulation in the North regions. Therefore, the different climate factors affecting SOC and TN sequestration in alfalfa occurred at a regional scale.

  16. Trace element geochemistry of Amba Dongar carbonatite complex, India: Evidence for fractional crystallization and silicate-carbonate melt immiscibility

    Indian Academy of Sciences (India)

    Jyotiranjan S Ray; P N Shukla

    2004-12-01

    Carbonatites are believed to have crystallized either from mantle-derived primary carbonate magmas or from secondary melts derived from carbonated silicate magmas through liquid immiscibility or from residual melts of fractional crystallization of silicate magmas. Although the observed coexistence of carbonatites and alkaline silicate rocks in most complexes, their coeval emplacement in many, and overlapping initial 87Sr/86Sr and 143Nd/144Nd ratios are supportive of their cogenesis; there have been few efforts to devise a quantitative method to identify the magmatic processes. In the present study we have made an attempt to accomplish this by modeling the trace element contents of carbonatites and coeval alkaline silicate rocks of Amba Dongar complex, India. Trace element data suggest that the carbonatites and alkaline silicate rocks of this complex are products of fractional crystallization of two separate parental melts. Using the available silicate melt-carbonate melt partition coefficients for various trace elements, and the observed data from carbonatites, we have tried to simulate trace element distribution pattern for the parental silicate melt. The results of the modeling not only support the hypothesis of silicate-carbonate melt immiscibility for the evolution of Amba Dongar but also establish a procedure to test the above hypothesis in such complexes.

  17. Matrix effects in nilotinib formulations with pH-responsive polymer produced by carbon dioxide-mediated precipitation

    DEFF Research Database (Denmark)

    Colombo, Stefano; Brisander, Magnus; Haglöf, Jakob;

    2015-01-01

    the drug dissolution, was characterized with a battery of physicochemical methodologies, including ToF-SIMS for surface composition, SAXS/WAXS and modulated DSC for crystallization characterization, and simultaneous UV-imaging and Raman spectroscopy for monitoring the dissolution process in detail...

  18. Single-crystal γ-MnS nanowires conformally coated with carbon.

    Science.gov (United States)

    Beltran-Huarac, Juan; Resto, Oscar; Carpena-Nuñez, Jennifer; Jadwisienczak, Wojciech M; Fonseca, Luis F; Weiner, Brad R; Morell, Gerardo

    2014-01-22

    We report for the first time the fabrication of single-crystal metastable manganese sulfide nanowires (γ-MnS NWs) conformally coated with graphitic carbon via chemical vapor deposition technique using a single-step route. Advanced spectroscopy and electron microscopy techniques were applied to elucidate the composition and structure of these NWs at the nanoscale, including Raman, XRD, SEM, HRTEM, EELS, EDS, and SAED. No evidence of α-MnS and β-MnS allotropes was found. The γ-MnS/C NWs have hexagonal cross-section and high aspect ratio (∼1000) on a large scale. The mechanical properties of individual γ-MnS/C NWs were examined via in situ uniaxial compression tests in a TEM-AFM. The results show that γ-MnS/C NWs are brittle with a Young's modulus of 65 GPa. The growth mechanism proposed suggests that the bottom-up fabrication of γ-MnS/C NWs is governed by vapor-liquid-solid mechanism catalyzed by bimetallic Au-Ni nanoparticles. The electrochemical performance of γ-MnS/C NWs as an anode material in lithium-ion batteries indicates that they outperform the cycling stability of stable micro-sized α-MnS, with an initial capacity of 1036 mAh g(-1) and a reversible capacity exceeding 503 mAh g(-1) after 25 cycles. This research advances the integration of carbon materials and metal sulfide nanostructures, bringing forth new avenues for potential miniaturization strategies to fabricate 1D core/shell heterostructures with intriguing bifunctional properties that can be used as building blocks in nanodevices. PMID:24392737

  19. Dielectric and electro-optic measurements of nematic liquid crystals doped with carbon nanotubes

    Science.gov (United States)

    Peterson, Matthew; Georgiev, Georgi; Atherton, Timothy; Cebe, Peggy

    We studied the effects of carbon nanotubes (CNTs) on the dielectric and electro-optic properties of nematic 5CB liquid crystals (LCs). Samples containing 0.01%, 0.10% and 1.00% CNTs by weight were prepared. Anti- parallel rubbed cells with a nominal thickness of 10 μm were prepared using indium tin oxide coated glass cells and a polyimide alignment layer. The capacitance and dissipation factor were measured using an Agilent 4284A precision LCR meter. From these measurements, the complex dielectric permittivity was determined as a function of frequency. Analysis of the low frequency regime (f <1000 Hz) indicates that 5CB samples containing CNTs have a higher conductance than neat samples. The Fréedericksz transition critical voltage was noted by a sharp increase in capacitance after an initial plateau. Numerical simulations of CNT-facilitated switching show that polarization induced on the nanotubes from capacitive effects can significantly reduce the critical voltage in DC electric fields, in agreement with experimental results. Measurements of the critical voltage over a range of frequencies will also be presented. Research was supported by the National Science Foundation, DMR1206010.

  20. The impact of carbon on single crystal nickel-base superalloys: Carbide behavior and alloy performance

    Science.gov (United States)

    Wasson, Andrew Jay

    Advanced single crystal nickel-base superalloys are prone to the formation of casting grain defects, which hinders their practical implementation in large gas turbine components. Additions of carbon (C) have recently been identified as a means of reducing grain defects, but the full impact of C on single crystal superalloy behavior is not entirely understood. A study was conducted to determine the effects of C and other minor elemental additions on the behavior of CMSX-4, a commercially relevant 2nd generation single crystal superalloy. Baseline CMSX-4 and three alloy modifications (CMSX-4 + 0.05 wt. % C, CMSX-4 + 0.05 wt. % C and 68 ppm boron (B), and CMSX-4 + 0.05 wt. % C and 23 ppm nitrogen (N)) were heat treated before being tested in high temperature creep and high cycle fatigue (HCF). Select samples were subjected to long term thermal exposure (1000 °C/1000 hrs) to assess microstructural stability. The C modifications resulted in significant differences in microstructure and alloy performance as compared to the baseline. These variations were generally attributed to the behavior of carbide phases in the alloy modifications. The C modification and the C+B modification, which both exhibited script carbide networks, were 25% more effective than the C+N modification (small blocky carbides) and 10% more effective than the baseline at preventing grain defects in cast bars. All C-modified alloys exhibited reduced as-cast gamma/gamma' eutectic and increased casting porosity as compared to baseline CMSX-4. The higher levels of porosity (volume fractions 0.002 - 0.005 greater than the baseline) were attributed to carbides blocking molten fluid flow during the final stages of solidification. Although the minor additions resulted in reduced solidus temperature by up to 16 °C, all alloys were successfully heat treated without incipient melting by modifying commercial heat treatment schedules. In the B-containing alloy, heat treatment resulted in the transformation of

  1. Anisotropy of sublimation from equivalent crystal faces of carbon-containing tungsten monocrystals

    Energy Technology Data Exchange (ETDEWEB)

    Dekhtyar, I.Ya.; Kolesnik, V.N.; Ovsienko, D.E.; Patoka, V.I.; Silant' ev, V.I.; Sosnina, E.I. (AN Ukrainskoj SSR, Kiev. Inst. Metallofiziki)

    1981-08-01

    Anisotropy of sublimation parameters was found in equivalent faces (100) or (1O0) of W single crystals oriented perpendicular or parallel to the growth direction. The anisotropy value depends on C concentration in W single crystals.

  2. Anisotropy of sublimation from equivalent crystal faces of carbon-containing tungsten monocrystals

    International Nuclear Information System (INIS)

    Anisotropy of sublimation parameters was found in equivalent faces (100) or (1O0) of W single crystals oriented perpendicular or parallel to the growth direction. The anisotropy value depends on C concentration in W single crystals

  3. Vapor diffusion method: Dependence of polymorphs and morphologies of calcium carbonate crystals on the depth of an aqueous solution

    Science.gov (United States)

    Liu, Qing; Wang, Hai-Shui; Zeng, Qiang

    2016-09-01

    The polymorph control of calcium carbonate by the vapor diffusion method is still a challenging issue because the resultant crystal polymorphs and morphologies highly depend on the experimental setup. In this communication, we demonstrated that the concentration gradients accompanied by the vapor diffusion method (ammonia concentration, pH and the ratio of CO32- to Ca2+ are changed with the solution depth and with time) are probably the main reasons to significantly affect the formation of crystal polymorphs. Raman, SEM and XRD data showed that calcite and vaterite crystals were preferred to nucleate and grow in the upper or the lower areas of aqueous solution respectively. The above results can be explained by the gradient effect.

  4. Hydrophilic Modification of Multi-Walled Carbon Nanotube for Building Photonic Crystals with Enhanced Color Visibility and Mechanical Strength

    Directory of Open Access Journals (Sweden)

    Feihu Li

    2016-04-01

    Full Text Available Low color visibility and poor mechanical strength of polystyrene (PS photonic crystal films have been the main shortcomings for the potential applications in paints or displays. This paper presents a simple method to fabricate PS/MWCNTs (multi-walled carbon nanotubes composite photonic crystal films with enhanced color visibility and mechanical strength. First, MWCNTs was modified through radical addition reaction by aniline 2,5-double sulfonic acid diazonium salt to generate hydrophilic surface and good water dispersity. Then the MWCNTs dispersion was blended with PS emulsion to form homogeneous PS/MWCNTs emulsion mixtures and fabricate composite films through thermal-assisted method. The obtained films exhibit high color visibility under natural light and improved mechanical strength owing to the light-adsorption property and crosslinking effect of MWCNTs. The utilization of MWCNTs in improving the properties of photonic crystals is significant for various applications, such as in paints and displays.

  5. Hydrothermal Synthesis of Metal-Polyphenol Coordination Crystals and Their Derived Metal/N-doped Carbon Composites for Oxygen Electrocatalysis.

    Science.gov (United States)

    Wei, Jing; Liang, Yan; Hu, Yaoxin; Kong, Biao; Zhang, Jin; Gu, Qinfen; Tong, Yuping; Wang, Xianbiao; Jiang, San Ping; Wang, Huanting

    2016-09-26

    Cobalt (or iron)-polyphenol coordination polymers with crystalline frameworks are synthesized for the first time. The crystalline framework is formed by the assembly of metal ions and polyphenol followed by oxidative self-polymerization of the organic ligands (polyphenol) during hydrothermal treatment in alkaline condition. As a result, such coordination crystals are even partly stable in strong acid (such as 2 m HCl). The metal (Co or Fe)-natural abundant polyphenol (tannin) coordination crystals are a renewable source for the fabrication of metal/carbon composites as a nonprecious-metal catalyst, which show high catalytic performance for both oxygen reduction reaction and oxygen evolution reaction. Such excellent performance makes metal-polyphenol coordination crystals an efficient precursor to fabricate low-cost catalysts for the large-scale application of fuel cells and metal-air batteries.

  6. Quantitative auger electron spectroscopy of the interface carbon layer formation on the vacuum cleavage surfaces of layered semiconductor In4Se3 crystals

    International Nuclear Information System (INIS)

    The results of the qualitative Auger electron spectroscopy of the interface carbon layer formation on the high vacuum cleavage surfaces of layered semiconductor In4Se3 crystals are presented. The kinetics of interfacial carbon layer formation on the cleavage surfaces of crystals and the elemental and phase composition of the interface dependent on the exposition time in high vacuum and on the dose of electron irradiation have been studied by the quantitative Auger electron and mass-spectroscopy methods

  7. Seasonal precipitation and soil moisture recharge as competing drivers of carbon and water fluxes across a gradient of semi-arid ecosystems

    Science.gov (United States)

    Maurer, G. E.; Litvak, M. E.

    2015-12-01

    Ecosystems of the southwestern U.S. receive precipitation in two prevailing weather patterns, the convective monsoon storms prevalent in late summer months, and synoptic-scale storm systems that are most frequent in late fall and winter. We examined a seven year record of eddy covariance data from six ecosystem types along an elevation/aridity gradient in the southwestern U.S. to determine the degree to which CO2 and H2O fluxes correlate with seasonal and interannual patterns in precipitation and soil water availability. Our results show that the majority of total annual primary production (GPP), ecosystem respiration (Reco), and evapotranspiration (ET) occurred during the monsoon season at most sites and in most years. During spring, typically the driest period in this region, the sites frequently had high rates of GPP and comparatively low Reco and ET, meaning this time period is important for annual carbon sequestration. Correlation between seasonal productivity measures and precipitation are generally weak, suggesting that some productivity peaks, such as the one in spring, are supported by stored soil water. We estimated the size of available soil water pools at multiple depths using extensive measurements of soil volumetric water content. Preliminary findings show strong relationships between seasonal CO2 and H2O fluxes and estimated available water in deeper soil layers. Our work indicates that relatively infrequent soil water recharge events are key to understanding the temporal distribution of ecosystem CO2 and H2O fluxes in the southwestern U.S., and potentially in other semi-arid ecosystems.

  8. Crystalline polymer decoration on multiwalled carbon nanotubes: MWCNT-induced P4VP periodic crystallization in CO2-expanded liquids

    Directory of Open Access Journals (Sweden)

    2011-01-01

    Full Text Available This work reports the functionalization of multi-walled carbon nanotubes (MWCNTs with crystalline poly(4- vinylpyridine (P4VP in CO2-expanded liquids (CXLs. The structure and morphology of MWCNT-induced polymer crystallization are examined, with the focus on molecular weight of P4VP (MW-P4VP, the pressure of CXLs and the concentration of P4VP. First, it is observed that the crystallization morphologies for the P4VP/MWCNTs composite with a low molecular weight P4VP (LMW-P4VP matrix could be finely controlled in CXLs, and it is surprising to find that the P4VP8700 wrapping patterns undergo a morphological evolution from dot crystals to dotted helical wrappings, and then to dense helical patterns by facile pressure tuning under lower polymer concentration. In other words, the CXLs method enables superior control of the P4VP crystallization patternings on MWCNTs, particularly efficient for LMW-P4VP at lower polymer concentration. Meanwhile, the CXL-assisted P4VP crystal growth mechanism on MWCNT is investigated, and the dominating growth mechanism is attributed to 'normal epitaxy' at lower P4VP concentration rather than 'soft epitaxy' at higher concentration. We believe that this work reports a new crystalline polymer wrapping approach in CXLs to noncovalent engineering of MWCNTs surfaces.

  9. A facile and low-cost length sorting of single-wall carbon nanotubes by precipitation and applications for thin-film transistors

    Science.gov (United States)

    Gui, Hui; Chen, Haitian; Khripin, Constantine Y.; Liu, Bilu; Fagan, Jeffrey A.; Zhou, Chongwu; Zheng, Ming

    2016-02-01

    Semiconducting single-wall carbon nanotubes (SWCNTs) with long lengths are highly desirable for many applications such as thin-film transistors and circuits. Previously reported length sorting techniques usually require sophisticated instrumentation and are hard to scale up. In this paper, we report for the first time a general phenomenon of a length-dependent precipitation of surfactant-dispersed carbon nanotubes by polymers, salts, and their combinations. Polyelectrolytes such as polymethacrylate (PMAA) and polystyrene sulfonate (PSS) are found to be especially effective on cholate and deoxycholate dispersed SWCNTs. By adding PMAA to these nanotube dispersions in a stepwise fashion, we have achieved nanotube precipitation in a length-dependent order: first nanotubes with an average length of 650 nm, and then successively of 450 nm, 350 nm, and 250 nm. A similar effect of nanotube length sorting has also been observed for PSS. To demonstrate the utility of the length fractionation, the 650 nm-long nanotube fraction was subjected to an aqueous two-phase separation to obtain semiconducting enriched nanotubes. Thin-film transistors fabricated with the resulting semiconducting SWCNTs showed a carrier mobility up to 18 cm2 (V s)-1 and an on/off ratio up to 107. Our result sheds new light on the phase behavior of aqueous nanotube dispersions under high concentrations of polymers and salts, and offers a facile, low-cost, and scalable method to produce length sorted semiconducting nanotubes for macroelectronics applications.Semiconducting single-wall carbon nanotubes (SWCNTs) with long lengths are highly desirable for many applications such as thin-film transistors and circuits. Previously reported length sorting techniques usually require sophisticated instrumentation and are hard to scale up. In this paper, we report for the first time a general phenomenon of a length-dependent precipitation of surfactant-dispersed carbon nanotubes by polymers, salts, and their

  10. The effects of warming-shifted plant phenology on ecosystem carbon exchange are regulated by precipitation in a semi-arid grassland.

    Directory of Open Access Journals (Sweden)

    Jianyang Xia

    Full Text Available BACKGROUND: The longer growing season under climate warming has served as a crucial mechanism for the enhancement of terrestrial carbon (C sink over the past decades. A better understanding of this mechanism is critical for projection of changes in C cycling of terrestrial ecosystems. METHODOLOGY/PRINCIPAL FINDINGS: A 4-year field experiment with day and night warming was conducted to examine the responses of plant phenology and their influences on plant coverage and ecosystem C cycling in a temperate steppe in northern China. Greater phenological responses were observed under night than day warming. Both day and night warming prolonged the growing season by advancing phenology of early-blooming species but without changing that of late-blooming species. However, no warming response of vegetation coverage was found for any of the eight species. The variances in species-level coverage and ecosystem C fluxes under different treatments were positively dependent upon the accumulated precipitation within phenological duration but not the length of phenological duration. CONCLUSIONS/SIGNIFICANCE: These plants' phenology is more sensitive to night than day warming, and the warming effects on ecosystem C exchange via shifting plant phenology could be mediated by precipitation patterns in semi-arid grasslands.

  11. Strontium hydroxyapatite and strontium carbonate as templates for the precipitation of calcium-phosphates in the absence and presence of fluoride

    Science.gov (United States)

    Sternitzke, Vanessa; Janousch, Markus; Heeb, Michèle B.; Hering, Janet G.; Johnson, C. Annette

    2014-06-01

    The heterogeneous precipitation of calcium-phosphates on calcium hydroxyapatite (Ca10(PO4)6(OH)2 or HAP) in the presence and absence of fluoride is important in the formation of bone and teeth, protection against tooth decay, dental and skeletal fluorosis and defluoridation of drinking water. Strontium hydroxyapatite (Sr10(PO4)6(OH)2 or SrHAP) and strontium carbonate (SrCO3) were used as calcium-free seed templates in precipitation experiments conducted with varying initial calcium-to-phosphate (Ca/P) or calcium-to-phosphate-to-fluoride (Ca/P/F) ratios. Suspensions of SrHAP or SrCO3 seed templates (which were calcium-limited for both templates and phosphate-limited in the case of SrCO3) were reacted at pH 7.3 (25 °C) over 3 days. The resulting solids were examined with Scanning Transmission Electron Microscopy (STEM), X-ray Diffraction (XRD), Fourier Transform Infrared (FTIR), and X-ray Photoelectron Spectroscopy (XPS), X-ray Absorption Near Edge Structure (XANES), and Extended X-ray Absorption Fine Structure spectroscopy (EXAFS). Calcium apatite was the predominant phase identified by all techniques independent of the added Ca/P ratios and of the presence of fluoride. It was not possible to make an unambiguous distinction between HAP and fluorapatite (Ca10(PO4)6F2, FAP). The apatite was calcium-deficient and probably contained some strontium.

  12. Genetic variation in seedling water-use efficiency of Patagonian Cypress populations from contrasting precipitation regimes assessed through carbon isotope discrimination

    Energy Technology Data Exchange (ETDEWEB)

    Pastorino, M. J.; Aparicio, A. G.; Marchelli, P.; Gallo, L. A.

    2012-11-01

    Water-use efficiency (WUE) is a physiological parameter that plays a significant role in the evolutionary dynamics of many forest tree species. It can be estimated indirectly through carbon isotope discrimination (A). In general, plants of more arid origins have lower values of A. In order to study the degree of genetic control of this parameter and the genetic variation in A of Patagonian Cypress seedlings, three Argentinean natural populations chosen to represent two contrasting precipitation regimes were sampled in a common garden trial. The dry situation was represented by two neighboring marginal forest patches from the steppe, while the humid condition was represented by a population with 1,200 mm higher mean annual precipitation. Height (H) and A were measured in 246 five-year-old seedlings from 41 open-pollinated families. The factor family had a significant effect on both variables; however heritability for A was found not to be significant in two out of the three populations. This could be explained by low sample size in one of them and by a real evolutionary effect in the other. An inverse association between H and A was verified, which is interpreted as evidence of an adaptation process at the intra-population level. The studied populations were not shown to discriminate carbon isotopes differently; hence evidence of adaptation to current environmental conditions could not be obtained. On the other hand, the arid populations proved to be quite different in terms of genetic variation, which seems to be the consequence of genetic drift and isolation. (Author) 49 refs.

  13. Interactions of carbon nanotubes in a nematic liquid crystal. I. Theory

    Science.gov (United States)

    Galerne, Yves

    2016-04-01

    Elongated and rodlike objects such as carbon nanotubes (CNTs) are studied when immersed in a nematic liquid crystal. Their interaction energy in a uniform nematic field depends on their orientation relative to the director n , and its minimum determines if they stabilize parallel or perpendicular to n . Using free energy calculations, we deduce the orientation at equilibrium that they choose in a uniform director field n or when they are in contact with a splay-bend disclination line. Naturally, the CNT orientations also depend on the anchoring conditions at their surface. Essentially, three types of anchorings are considered, planar, homeotropic, and Janus anchorings in the cases of weak and strong anchoring strengths. In the presence of a splay-bend disclination line, they are attracted toward it and ultimately, they get out of the colloidal dispersion to stick on it. Their orientation relative to the line is found to be parallel or perpendicular to it, again depending on the anchoring conditions. When a sufficient number of particles are deposited on a disclination line, we finally obtain a micro- or nanonecklace in the shape of a thin thread or of a bottle brush, according to the CNTs being oriented parallel or perpendicular to the disclination line, respectively. The system exhibits a rich versatility even if up to now the weak anchorings appear to be difficult to control. As discussed in the associated experimental paper, these necklaces could be a step toward interesting applications for realizing nanowires self-connected in three dimensions to predesignated electrodes. This method could provide a way to increase the number of transistors that may be connected together on a small volume.

  14. Crystallization and mechanical properties of functionalized single-walled carbon nanotubes/polyvinylidene fluoride composites

    DEFF Research Database (Denmark)

    Ma, Jing; Iftekharul Haque, Rubaiyet; Larsen, Mikael

    2012-01-01

    Single-walled carbon nanotubes were purified and functionalized by nitric acid and octadecylamine. Raman and Fourier transform infrared spectroscopy were used to characterize the functionalization of the single-walled carbon nanotubes. Polyvinylidene flouride nanocomposites containing 1 wt......% purified or functionalized single-walled carbon nanotubes were prepared by solution blending and injection molding. The dispersion of different carbon nanotubes in dimethylformamide and in polyvinylidene flouride has been investigated. Mechanical properties show that adding single-walled carbon nanotubes...

  15. Vacuum filtration based formation of liquid crystal films of semiconducting carbon nanotubes and high performance transistor devices

    International Nuclear Information System (INIS)

    In this paper, we report ultra-thin liquid crystal films of semiconducting carbon nanotubes using a simple vacuum filtration process. Vacuum filtration of nanotubes in aqueous surfactant solution formed nematic domains on the filter membrane surface and exhibited local ordering. A 2D fast Fourier transform was used to calculate the order parameters from scanning electron microscopy images. The order parameter was observed to be sensitive to the filtration time demonstrating different regions of transformation namely nucleation of nematic domains, nanotube accumulation and large domain growth.Transmittance versus sheet resistance measurements of such films resulted in optical to dc conductivity of σ opt/σ dc = 9.01 indicative of purely semiconducting nanotube liquid crystal network.Thin films of nanotube liquid crystals with order parameters ranging from S = 0.1–0.5 were patterned into conducting channels of transistor devices which showed high I on/I off ratios from 10–19 800 and electron mobility values μ e = 0.3–78.8 cm2 (V-s)−1, hole mobility values μ h = 0.4–287 cm2 (V-s)−1. High I on/I off ratios were observed at low order parameters and film mass. A Schottky barrier transistor model is consistent with the observed transistor characteristics. Electron and hole mobilities were seen to increase with order parameters and carbon nanotube mass fractions. A fundamental tradeoff between decreasing on/off ratio and increasing mobility with increasing nanotube film mass and order parameter is therefore concluded. Increase in order parameters of nanotubes liquid crystals improved the electronic transport properties as witnessed by the increase in σ dc/σ opt values on macroscopic films and high mobilities in microscopic transistors. Liquid crystal networks of semiconducting nanotubes as demonstrated here are simple to fabricate, transparent, scalable and could find wide ranging device applications. (papers)

  16. Final Report: The Impact of Carbonate on Surface Protonation, Electron Transfer and Crystallization Reactions in Iron Oxide Nanoparticles and Colloids

    Energy Technology Data Exchange (ETDEWEB)

    Dixon, David Adams [The University of Alabama

    2013-07-02

    This project addresses key issues of importance in the geochemical behavior of iron oxides and in the geochemical cycling of carbon and iron. For Fe, we are specifically studying the influence of carbonate on electron transfer reactions, solid phase transformations, and the binding of carbonate to reactive sites on the edges of particles. The emphasis on carbonate arises because it is widely present in the natural environment, is known to bind strongly to oxide surfaces, is reactive on the time scales of interest, and has a speciation driven by acid-base reactions. The geochemical behavior of carbonate strongly influences global climate change and CO{sub 2} sequestration technologies. Our goal is to answer key questions with regards to specific site binding, electron transfer reactions, and crystallization reactions of iron oxides that impact both the geochemical cycling of iron and CO{sub 2} species. Our work is focused on the molecular level description of carbonate chemistry in solution including the prediction of isotope fractionation factors. We have also done work on critical atmospheric species.

  17. Carbon Mineralization by Aqueous Precipitation for Beneficial Use of CO2 from Flue Gas

    Energy Technology Data Exchange (ETDEWEB)

    Devenney, Martin [Calera Corporation, Moss Landing, CA (United States); Gilliam, Ryan [Calera Corporation, Moss Landing, CA (United States); Seeker, Randy [Calera Corporation, Moss Landing, CA (United States)

    2015-06-30

    The objective of this project was to demonstrate an innovative process to mineralize CO2 from flue gas directly to reactive carbonates and maximize the value and versatility of its beneficial use products. The program scope includes the design, construction, and testing of a CO2 Conversion to Material Products (CCMP) Pilot Demonstration Plant utilizing CO2 from the flue gas of a power production facility in Moss Landing, CA as well as flue gas from coal combustion. This final report details all development, analysis, design and testing of the project. Also included in the final report are an updated Techno-Economic Analysis and CO2 Lifecycle Analysis. The subsystems included in the pilot demonstration plant are the mineralization subsystem, the Alkalinity Based on Low Energy (ABLE) subsystem, the waste calcium oxide processing subsystem, and the fiber cement board production subsystem. The fully integrated plant was proven to be capable of capturing CO2 from various sources (gas and coal) and mineralizing it into a reactive calcium carbonate binder and subsequently producing commercial size (4ftx8ft) fiber cement boards. The final report provides a description of the “as built” design of these subsystems and the results of the commissioning activities that have taken place to confirm operability. The report also discusses the results of the fully integrated operation of the facility. Fiber cement boards have been produced in this facility exclusively using reactive calcium carbonate from captured CO2 from flue gas. These boards meet all US and China appropriate acceptance standards. Use demonstrations for these boards are now underway.

  18. Experience with a carbon injection system at a spray dryer/electrostatic precipitator equipped waste-to-energy facility

    Energy Technology Data Exchange (ETDEWEB)

    Honeycheck, T.S.; Gesell, G. [American Ref-Fuel Co., Houston, TX (United States); Armellino, K.E. [American Ref-Fuel Co., Uniondale, NY (United States); Kozlowski, J. [American Ref-Fuel Co. of Essex County, Newark, NJ (United States)

    1997-12-01

    American Ref-Fuel Company of Essex County obtained an air permit to construct the Essex County Resource Recovery Facility (ECRRF), a municipal solid waste resource recovery facility, in December 1985 from the New Jersey Department of Environmental Protection (NJDEP). Permit condition A.9.a. states that the emission rate of mercury from each unit shall not exceed 0.053 pounds per hour, based on the average value of three runs using EPA Method 101A. Testing for mercury was required to be performed on a quarterly basis during the facility`s first year of operation. This emission requirement was met by the spray dryer adsorber (SDA)/electrostatic precipitator (ESP) equipped facility. Subsequently, the NJDEP chartered a task force to investigate the setting of a new statewide mercury emission standard for municipal solid waste (MSW) combustors. The task force in July of 1993 recommended a more stringent two phase emission standard requiring all facilities to achieve 65 {mu}g/dscm at 7% oxygen dry volume or 80 % reduction by January, 1996, and to achieve 28 {mu}g/dscm at 7% oxygen dry volume or 80% reduction by January 1, 2000. These recommendations and a requirement for installing a mercury control system were codified into a regulation in November 22, 1994. In order to comply with the new regulation the facility proceeded with a retrofit mercury control system.

  19. Molecular dynamics simulation of melting and crystallization processes of polyethylene clusters confined in armchair single-walled carbon nanotubes.

    Science.gov (United States)

    Zhou, Zhou; Wang, Jinjian; Zhu, Xiaolei; Lu, Xiaohua; Guan, Wenwen; Yang, Yuchen

    2015-01-01

    The confined interaction is important to understand the melting and crystallization of polymers within single-wall carbon tube (SWNT). However, it is difficult for us to observe this interaction. In the current work, the structures and behaviors of melting and crystallization for polyethylene (PE) clusters confined in armchair single-walled carbon nanotubes ((n,n)-SWNTs) are investigated and examined based on molecular dynamics (MD) simulations. The nonbonded energies, structures, Lindemman indices, radial density distributions, and diffusion coefficients are used to demonstrate the features of melting phase transition for PE clusters confined in (n,n)-SWNTs. The chain end-to-end distance (R(n)) and chain end-to-end distribution are used to examine the flexibility of the PE chain confined in SWNT. The global orientational order parameter (P2) is employed to reveal the order degree of whole PE polymer. The effect of polymerization degree on melting temperature and the influence of SWNT chirality on structure of PE cluster are examined and discussed. Results demonstrate that within the confined environment of SWNT, PE clusters adopt novel co-axial crystalline layer structure, in which parallel chains of each layer are approximately vertical to tube axis. The disordered-ordered transformation of PE chains in each layer is an important structural feature for crystallization of confined PE clusters. SWNTs have a considerable effect on the structures and stabilities of the confined PE clusters.

  20. Seasonal and Interannual Variations of Evaporation and their Relations with Precipitation, Net Radiation, and Net Carbon Accumulation for the Gediz Basin Area

    Science.gov (United States)

    Choudhury, Bhaskar J.

    1999-01-01

    A model combining the rate of carbon assimilation with water and energy balance equations has been run using satellite and ancillary data for a period of 60 months (January 1986 to December 1990). Calculations for the Gediz basin area give mean annual evaporation as 395 mm, which is composed of 45% transpiration, 42% soil evaporation and 13% interception. The coefficient of interannual variation of evaporation is found to be 6%, while that for precipitation and net radiation are, respectively, 16% and 2%, illustrating that net radiation has an important effect in modulating interannual variation of evaporation. The mean annual water use efficiency (i.e., the ratio of net carbon accumulation and total evaporation) is ca. 1 g/sq m/mm, and has a coefficient of interannual variation of 5%. A comparison of the mean water use efficiency with field observations suggests that evaporation over the area is utilized well for biomass production. The reference crop evaporation for irrigated areas has annual mean and coefficient of variation as, respectively, 1176 mm and 3%. The total evaporation during three summer months of peak evaporation (June-August) is estimated to be about 575 mm for irrigated crops like maize and cotton. Seasonal variations of the fluxes are presented.

  1. Precipitação de carbonato de cálcio para aplicação industrial Calcium carbonate precipitation for industrial application

    Directory of Open Access Journals (Sweden)

    Felipe Ventura Oliveira

    2009-06-01

    Full Text Available Esse trabalho apresenta os resultados experimentais da síntese de partículas de carbonato de cálcio precipitado (PCC depositadas sobre carbonato de cálcio natural (GCC, onde se variaram a relação [Ca]/[CO3]T inicial, a temperatura e o pH da solução aquosa de síntese e a concentração de coagulante (EDTA. As amostras foram caracterizadas por microscopia eletrônica de varredura, carbono total (TOC, área superficial específica (método BET, distribuição granulométrica e refletância de luz visível para se determinar o brilho. Os resultados foram comparados a amostras de referência utilizadas por indústrias de papel. O aumento do teor de EDTA favoreceu a coagulação das partículas de PCC entre si, aumentando o tamanho dos agregados. Em valores de pH entre 10 e 11, o PCC tendeu a coagular entre si e, em valores de pH entre 8 e 9, na superfície das partículas de GCC. Observou-se uma redução da densidade do material obtido. Os valores de área superficial específica do material estão dentro do aceitável pelas indústrias de papel e de plásticos.This work presents the experimental results for precipitated calcium carbonate (PCC synthesis over a ground calcium carbonate (GCC substrate. The parameters [Ca]/[CO3]T initial ratio, aqueous synthesis solution temperature, pH and coagulant concentration (EDTA were investigated. The samples were characterized by scanning electron microscopy (SEM, total carbon (TOC, specific surface area (BET method, particle size distribution and visible light reflectance (to measure the brightness of the samples. The results were compared with values from standard samples used in the paper industry. According to the experimental results, it was noted that an increase in the EDTA amount added to the pulp favored PCC homo-coagulation and also increased the size of the coagulum. PCC tends to homo-coagulate between pH 10 and 11, while it tends to precipitate over GCC particles between pH 8 and 9. A

  2. Para-amino benzoic acid–mediated synthesis of vaterite phase of calcium carbonate

    Indian Academy of Sciences (India)

    T N Ramesh; S A Inchara; K Pallavi

    2015-05-01

    Calcium carbonate polymorphs were precipitated at room temperature and 80°C by varying the precipitation pH, carbonate source, effect of solvent in presence and absence of structure directing agent such as para-aminobenzoic acid. Calcite phase of calcium carbonate was obtained when sodium hydrogen carbonate and/or sodium carbonate (used as precipitating agents) were added to calcium chloride solution at different pHs in water and/or methanol as solvent in separate experiments. Vaterite phase of calcium carbonate (CaCO3) has been synthesized by mixing calcium chloride and sodium carbonate in presence of para-aminobenzoic acid when water–methanol binary mixture was used as solvent. Vaterite phase of calcium carbonate crystallizes in P63/mmc, while that of calcite phase in R-3mc, respectively. Calcite phase of calcium carbonate exhibits rhombohedral morphology, while vaterite phase has spherical morphology.

  3. Effect of epicuticular wax crystals on the localization of artificially deposited sub-micron carbon-based aerosols on needles of Cryptomeria japonica.

    Science.gov (United States)

    Nakaba, Satoshi; Yamane, Kenichi; Fukahori, Mie; Nugroho, Widyanto Dwi; Yamaguchi, Masahiro; Kuroda, Katsushi; Sano, Yuzou; Wuled Lenggoro, I; Izuta, Takeshi; Funada, Ryo

    2016-09-01

    Elucidation of the mechanism of adsorption of particles suspended in the gas-phase (aerosol) to the outer surfaces of leaves provides useful information for understanding the mechanisms of the effect of aerosol particles on the growth and physiological functions of trees. In the present study, we examined the localization of artificially deposited sub-micron-sized carbon-based particles on the surfaces of needles of Cryptomeria japonica, a typical Japanese coniferous tree species, by field-emission scanning electron microscopy. The clusters (aggregates) of carbon-based particles were deposited on the needle surface regions where epicuticular wax crystals were sparsely distributed. By contrast, no clusters of the particles were found on the needle surface regions with dense distribution of epicuticular wax crystals. Number of clusters of carbon-based particles per unit area showed statistically significant differences between regions with sparse epicuticular wax crystals and those with dense epicuticular wax crystals. These results suggest that epicuticular wax crystals affect distribution of carbon-based particles on needles. Therefore, densely distributed epicuticular wax crystals might prevent the deposition of sub-micron-sized carbon-based particles on the surfaces of needles of Cryptomeria japonica to retain the function of stomata.

  4. Utilizing carbon nanotube electrodes to improve charge injection and transport in bis(trifluoromethyl)-dimethyl-rubrene ambipolar single crystal transistors.

    Science.gov (United States)

    Xie, Wei; Prabhumirashi, Pradyumna L; Nakayama, Yasuo; McGarry, Kathryn A; Geier, Michael L; Uragami, Yuki; Mase, Kazuhiko; Douglas, Christopher J; Ishii, Hisao; Hersam, Mark C; Frisbie, C Daniel

    2013-11-26

    We have examined the significant enhancement of ambipolar charge injection and transport properties of bottom-contact single crystal field-effect transistors (SC-FETs) based on a new rubrene derivative, bis(trifluoromethyl)-dimethyl-rubrene (fm-rubrene), by employing carbon nanotube (CNT) electrodes. The fundamental challenge associated with fm-rubrene crystals is their deep-lying HOMO and LUMO energy levels, resulting in inefficient hole injection and suboptimal electron injection from conventional Au electrodes due to large Schottky barriers. Applying thin layers of CNT network at the charge injection interface of fm-rubrene crystals substantially reduces the contact resistance for both holes and electrons; consequently, benchmark ambipolar mobilities have been achieved, reaching 4.8 cm(2) V(-1) s(-1) for hole transport and 4.2 cm(2) V(-1) s(-1) for electron transport. We find that such improved injection efficiency in fm-rubrene is beneficial for ultimately unveiling its intrinsic charge transport properties so as to exceed those of its parent molecule, rubrene, in the current device architecture. Our studies suggest that CNT electrodes may provide a universal approach to ameliorate the charge injection obstacles in organic electronic devices regardless of charge carrier type, likely due to the electric field enhancement along the nanotube located at the crystal/electrode interface. PMID:24175573

  5. One-dimensional SnF2 single crystals in the inner channels of single-wall carbon nanotubes: I. Preparation and basic characterization

    International Nuclear Information System (INIS)

    One-dimensional (1D) SnF2 single crystals have been obtained by crystallization from melt in the inner channels of single-wall carbon nanotubes (SWCNTs). SWCNTs with an inner diameter of 1.02-1.4 nm, synthesized by electric-arc discharge and chemically purified, were used for incorporation. The synthesized 1D SnF2 single crystal-SWCNT composites are basically characterized by X-ray diffraction, energy-dispersive analysis, electron microscopy, and chemical analysis. The characteristic motifs of tin cation distribution in the SWCNT inner channel confirm the formation of SnF2 single crystals.

  6. ELECTRICAL RESISTIVITY, CRYSTALLIZATION AND MECHANICAL PROPERTIES OF POLYPROPYLENE/MULTI-WALLED CARBON NANOTUBE/CALCIUM CARBONATE COMPOSITES PREPARED BY MELT MIXING

    Institute of Scientific and Technical Information of China (English)

    Ha-da Bao; Zhao-xia Guo; Jian Yu

    2009-01-01

    Polypropylene (PP)/multi-walled carbon nanotube (MWCNT)/calcium carbonate (CaCO3) composites are prepared by melt mixing using two types of CaCO3 of different sizes. The electrical resistivities of the composites with the two types of CaCO3 are all lower than those of the corresponding PP/MWCNT composites at various MWCNT loadings (1 wt%-5 wt%). The morphology of the composites is investigated by field emission scanning electron microscopy (FESEM). The crystallization behavior of PP in the composites is characterized by differential scanning calorimetry (DSC). The storage modulus, as measured by dynamic mechanical analysis (DMA), increases significantly by the presence of CaCO3.

  7. Photoinduced crystallization of calcium carbonate from a homogeneous precursor solution in the presence of partially hydrolyzed poly(vinyl alcohol)

    Science.gov (United States)

    Nishio, Takashi; Naka, Kensuke

    2015-04-01

    Photoinduced crystallization of calcium carbonate (CaCO3) was demonstrated by the photodecarboxylation of ketoprofen (KP, 2-(3-benzoylphenyl)propionic acid) under alkaline conditions (pH 10). In this method, a homogeneous solution comprising KP, calcium chloride, ammonia, and partially hydrolyzed poly(vinyl alcohol) (PVAPS, degree of saponification: 86.5-89.0 mol %) was used as the precursor solution and was exposed to ultraviolet (UV) irradiation for different time periods. Thermogravimetric analysis of the obtained xerogels showed that increasing the UV irradiation time increased the amount of CaCO3 formed and the complete conversion of calcium ions to calcite was achieved after 50 min of UV irradiation. Furthermore, solid phase analyses suggested that nanometer-to-micron-sized calcite crystals were formed and dispersed in the obtained PVAPS matrix.

  8. Growth of single-crystal α-MnO2 nanorods on multi-walled carbon nanotubes

    International Nuclear Information System (INIS)

    Single-crystal α-MnO2 nanorods were grown on multi-walled carbon nanotubes (MWNTs) in H2SO4 aqueous solution. The morphology and microstructure of the composites were examined by transmission electron microscopy, high-resolution transmission electron microscopy (HRTEM), X-ray diffractometry and energy dispersive spectroscopy (EDS). The results show that α-MnO2 single-crystal nanorods with a mean diameter of 15 nm were densely grown on the surface of MWNTs. Those MWNTs/MnO2 composites were used as an electrode material for supercapacitors, and it was found that the supercapacitor performance using MWNTs/MnO2 composites was improved largely compared to that using pure MWNTs and α-MnO2 nanorod mechanically mixed with MWNTs

  9. Interactions of carbon nanotubes in a nematic liquid crystal. II. Experiment

    Science.gov (United States)

    Agha, Hakam; Galerne, Yves

    2016-04-01

    Multiwall carbon nanotube (CNT) colloids with different anchoring conditions are dispersed in pentyl-cyanobiphenyl (5CB), a thermotropic liquid crystal (LC) that exhibits a room-temperature nematic phase. The experiments make use of CNTs treated for strong planar, homeotropic, or Janus anchorings. Observations with a polarizing microscope show that the CNTs placed in a uniform nematic field stabilize parallel or perpendicular to n depending on their anchoring conditions. In the presence of a splay-bend disclination line, they are first attracted toward it and ultimately, they get trapped on it. Their orientation relative to the line is then found to be parallel or perpendicular to it, again depending on the anchoring conditions. When a sufficient number of particles are deposited on a disclination line, they form a micro- or nanonecklace in the shape of a thin thread or of a bottle brush, with the CNTs being oriented parallel or perpendicular to the disclination line according to the anchoring treatment. The system exhibits a rich versatility, even if until now the weak anchorings appear to be difficult to control. In a next step, the necklaces may be glued by means of pyrrole electropolymerization. In this manner, we realize a true materialization of the disclination lines, and we obtain nanowires capable of conducting the electricity in the place of the initial disclinations that just worked as templates. The advantage of the method is that it finally provides nanowires that are automatically connected to predesignated three-dimensional (3D) electrodes. Such a 3D nanowiring could have important applications, as it could allow one to develop electronic circuits in the third dimension. They could thus help with increasing the transistor density per surface unit, although downsizing of integrated circuits will soon be limited to atomic sizes or so. In other words, the predicted limitation to Moore's law could be avoided. For the moment, the nanowires that we obtain

  10. Recovery of N and P from human urine by freezing, struvite precipitation and adsorption to zeolite and active carbon.

    Science.gov (United States)

    Ganrot, Zsófia; Dave, Göran; Nilsson, Eva

    2007-11-01

    The majority of the nutrients in domestic waste originate from human urine. This study deals with methods for recovery of N and P from urine. Results from a freezing-thawing method (FTM) together with struvite recovery and nitrogen adsorption on zeolite and active carbon (AC) are presented. Various amounts of MgO, zeolite and AC were added to samples of 100ml urine. After 3 days the supernatants were analysed for pH, total-N, total-P and acute toxicity for Daphnia magna. One set of samples was frozen and then thawed and the supernatants collected were tested as before. The FTM method concentrated 60% of the nutrients in 40% of the initial volume and significantly improved the N reduction and D. magna survival. The P recovery was 95-100%, mainly as struvite. No significant effect of AC was found. Zeolite improved the P recovery and in some combinations of MgO also the N recovery. PMID:17321132

  11. Probing local pH-based precipitation processes in self-assembled silica-carbonate hybrid materials.

    Science.gov (United States)

    Opel, Julian; Hecht, Mandy; Rurack, Knut; Eiblmeier, Josef; Kunz, Werner; Cölfen, Helmut; Kellermeier, Matthias

    2015-11-01

    Crystallisation of barium carbonate in the presence of silica can lead to the spontaneous assembly of highly complex superstructures, consisting of uniform and largely co-oriented BaCO3 nanocrystals that are interspersed by a matrix of amorphous silica. The formation of these biomimetic architectures (so-called silica biomorphs) is thought to be driven by a dynamic interplay between the components, in which subtle changes of conditions trigger ordered mineralisation at the nanoscale. In particular, it has been proposed that local pH gradients at growing fronts play a crucial role in the process of morphogenesis. In the present work, we have used a special pH-sensitive fluorescent dye to directly trace these presumed local fluctuations by means of confocal laser scanning microscopy. Our data demonstrate the existence of an active region near the growth front, where the pH is locally decreased with respect to the alkaline bulk solution on a length scale of few microns. This observation provides fundamental and, for the first time, direct experimental support for the current picture of the mechanism underlying the formation of these peculiar materials. On the other hand, the absence of any temporal oscillations in the local pH - another key feature of the envisaged mechanism - challenges the notion of autocatalytic phenomena in such systems and raises new questions about the actual role of silica as an additive in the crystallisation process. PMID:26439927

  12. CRYSTALLIZATION AND MORPHOLOGY OF STAR-SHAPED POLYETHYLENOXYDE-b-POLYCAPROLACTONE UNDER HIGH PRESSURE CARBON DIOXIDE

    Institute of Scientific and Technical Information of China (English)

    Ya Li; Jian Zhou; Jun Li; Qu-ting Gou; Qun Gu; Zong-bao Wang

    2012-01-01

    Atomic force microscopy (AFM),wide-angle X-ray diffraction (WAXD) and differential scanning calorimetry are used to analyze the crystallization morphology and melting behavior of 4-arm PEO-b-PCL under high-pressure CO2.It is demonstrated that CO2 has certain effect on the melting and crystallization behavior of the samples.After crystallization under CO2 at 4 MPa,spherulites with concentric ring-banded structure are formed which are composed of crystals with periodic thickness variation,and the band distance decreases with increasing treatment pressure.Due to the plasticization effect of CO2,depression of the melting temperature is observed with sorption of CO2 in polymers.

  13. Unexpected carbon-oxygen bond cleavage of THF promoted by guanidinate titanium complex/lithium diisopropylamide: Synthesis and crystal structure

    Institute of Scientific and Technical Information of China (English)

    ZHANG Yong; WANG Mei; YAO Yingming; SHEN Qi

    2005-01-01

    An unexpected carbon-oxygen bond cleavage of THF (THF = tetrahydrofuran) promoted by guanidinate titanium complex was described. Guanidinate lithium [Pr2iNC(NCy)2]Li (Cy = cyclohexyl) formed in situ reacted with TiCl4(THF)2 in a 2:1 molar ratio to produce the guanidinate titanium chloride [Pr2iNC(NCy)2]2TiCl2 (1) in good yield. The reaction of [Pr2iNC(NCy)2]2TiCl2 with lithium diisopropylamide in THF afforded an unexpected [Pr2iNC(NCy)2]2Ti(OBun)2 (2), which was formed by the cleavage of carbon-oxygen bond of THF. Complexes 1 and 2 were fully characterized by elemental analysis, NMR and IR spectroscopies, and X-ray crystal structure determination for complex 2.

  14. The effect of crystallization pressure on macromolecular structure, phase evolution, and fracture resistance of nano-calcium carbonate-reinforced high density polyethylene

    International Nuclear Information System (INIS)

    We describe here phase evolution and structural changes that are induced when high density polyethylene (HDPE) containing dispersion of nano-calcium carbonate is isothermally crystallized in the pressure range of 0.1-100 MPa. To delineate and separate the effects of applied crystallization pressure from nanoparticle effects, a relative comparison is made between neat HDPE and HDPE containing nano-calcium carbonate under similar experimental conditions. X-ray diffraction studies point toward the evolution of monoclinic phase at high crystallization pressure together with the commonly observed orthorhombic phase of HDPE. Furthermore, the nucleation of monoclinic phase is promoted by nanoparticles even at low crystallization pressure. The equilibrium melting point is insignificantly influenced on the addition of nanoparticle, such that the crystallization pressure has no obvious effect. The strong thermodynamic interaction between nano-calcium carbonate and HDPE is supported by the shift in glass transition temperature and changes in the modification of absorption bands of HDPE in Fourier transform infrared (FTIR) spectrum. Furthermore, the reinforcement of HDPE with nano-calcium carbonate increases impact strength and alters the micromechanism from crazing-tearing in polyethylene to fibrillated fracture in polymer nanocomposite, such that the fibrillation increases with crystallization pressure.

  15. Crystal Structure of PhnH: an Essential Component of Carbon-Phosphorus Lyase in Escherichia coli

    Energy Technology Data Exchange (ETDEWEB)

    Adams,M.; Luo, Y.; Hove-Jensen, B.; He, S.; van Staalduinen, L.; Zechel, D.; Jia, Z.

    2008-01-01

    Organophosphonates are reduced forms of phosphorous that are characterized by the presence of a stable carbon-phosphorus (C-P) bond, which resists chemical hydrolysis, thermal decomposition, and photolysis. The chemically inert nature of the C-P bond has raised environmental concerns as toxic phosphonates accumulate in a number of ecosystems. Carbon-phosphorous lyase (CP lyase) is a multienzyme pathway encoded by the phn operon in gram-negative bacteria. In Escherichia coli 14 cistrons comprise the operon (phnCDEFGHIJKLMNOP) and collectively allow the internalization and degradation of phosphonates. Here we report the X-ray crystal structure of the PhnH component at 1.77 Angstroms resolution. The protein exhibits a novel fold, although local similarities with the pyridoxal 5'-phosphate-dependent transferase family of proteins are apparent. PhnH forms a dimer in solution and in the crystal structure, the interface of which is implicated in creating a potential ligand binding pocket. Our studies further suggest that PhnH may be capable of binding negatively charged cyclic compounds through interaction with strictly conserved residues. Finally, we show that PhnH is essential for C-P bond cleavage in the CP lyase pathway.

  16. Crystallization behavior and thermal stability of poly(butylene succinate)/poly(propylene carbonate) blends prepared by novel vane extruder

    Science.gov (United States)

    Chen, Rongyuan; Zou, Wei; Zhang, Haichen; Zhang, Guizhen; Qu, Jinping

    2016-03-01

    This work focused on the study of crystallization behavior and thermal stability of degradable poly(butylene succinate) (PBS) and poly(propylene carbonate) (PPC) blends prepared by vane extruder based on elongation force field, which is novel equipment for polymer processing. Dicumyl peroxide (DCP) was applied in this work as compatibilizer for PBS/PPC blend. Crystallization behavior and melting behavior of the blends were investigated by differential scanning calorimetry (DSC) testing. Thermal stability of the blends was studied by thermogravimetric (TG) testing. Furthermore, the melt flow indices (MFI) of the blends were examined by a MFI instrument. The results showed that the crystallization temperature of PBS decreased with the addition of PPC and DCP. The glass transition temperature of PPC increased and the melting temperature of the blend increased with the addition of PPC and DCP, which indicated that the entanglement between the molecular chains of PBS and PPC was enhanced. Thermogravimetric analysis showed that a two-step decomposition process of the blend occurred due to the different thermal resistance of PBS and PPC, and the addition of PBS reduced the decomposition rate of PPC. Moreover, the addition of PBS improved the melt flow property of PPC.

  17. Effects of Tx-100-SDS on crystal growth of calcium carbonate in reverse microemulsion solution

    Institute of Scientific and Technical Information of China (English)

    TANG Yu; DU BiYing; LI LinGang; YANG Jun; ZHANG YuanMing

    2007-01-01

    Syntheses of CaCO3 crystals in reverse microemulsion solutions containing 1-(1,1,3,3-tetramethylbutyl)-4-hydroxypolyethoxybenzene (Tx-100), sodium dodecyl sulfate (SDS) and their equimolar mixture were carried out at room temperature respectively. The crystal phase of CaCO3 is changed from calcite at low concentrations to vaterite at high concentrations of SDS and Tx-100. From rods at low concentration to olivary spheres at high concentration, SDS can influence the morphology of CaCO3 significantly, while almost no such effect for Tx-100. Hollow spheres, olivary spheres and even two fused olivary spheres of CaCO3 were produced at different concentrations of Tx-100-SDS, and the variation of crystal phase is opposite to that in the presence of SDS or Tx-100 alone. The effects of interaction of SDS with Tx-100 on morphology and crystal phase of CaCO3 were discussed. It was estimated to put forward that the formation of hollow CaCO3 crystals was caused by the collaborating actions of SDS template and TX-100 inhibition.

  18. New Insights into the Origin of Magnetite Crystals in ALH84001 Carbonate Disks

    Science.gov (United States)

    Thomas-Keptra, Katie L.; Clemett, S. J.; Wentworth S. J.; Mckay, D. S.; Gibson, E. K., Jr.

    2010-01-01

    Martian meteorite ALH84001 preserves evidence of interaction with aqueous fluids while on Mars in the form of microscopic carbonate disks believed to have formed approx.3.9 Ga ago at beginning of the Noachian epoch. Intimately associated within and throughout these carbonate disks are nanocrystal magnetites (Fe3O4) with unusual chemical and physical properties, whose ori gins have become the source of considerable debate. One group of hypotheses argues that these magnetites are the product of partial thermal decomposition of the host carbonate. Alternatively, the origins of magnetite and carbonate may be unrelated: that is, from the perspective of the carbonate the magnetite is allochthonous. We have sought to resolve between these hypotheses through the detailed characterized of the compositional and structural relationships between the carbonate disks, their associated magnetites and the orthopyroxene matrix in which they are embedded [1]. Comparison of these results with experimental thermal decomposition studies of sideritic carbonates conducted under a range of heating scenarios suggests that the magnetite nanocrystals in the ALH84001 carbonate disks are not the products of thermal decomposition.

  19. A Study of the Optical Properties of Ice Crystals with Black Carbon Inclusions

    Energy Technology Data Exchange (ETDEWEB)

    Arienti, Marco [Sandia National Laboratories (SNL-CA), Livermore, CA (United States); Yang, Xiaoyuan [Sandia National Laboratories (SNL-CA), Livermore, CA (United States); Kopacz, Adrian M [Sandia National Laboratories (SNL-CA), Livermore, CA (United States); Geier, Manfred [Sandia National Laboratories (SNL-CA), Livermore, CA (United States)

    2015-09-01

    The report focu ses on the modification of the optical properties of ice crystals due to atmospheric black car bon (BC) contamination : the objective is to advance the predictive capabilities of climate models through an improved understanding of the radiative properties of compound particles . The shape of the ice crystal (as commonly found in cirrus clouds and cont rails) , the volume fraction of the BC inclusion , and its location inside the crystal are the three factors examined in this study. In the multiscale description of this problem, where a small absorbing inclusion modifies the optical properties of a much la rger non - absorbing particle, state - of - the - art discretization techniques are combined to provide the best compromise of flexibility and accuracy over a broad range of sizes .

  20. Bacterially induced precipitation of CaCO sub 3 : An example from studies of cyanobacterial mats

    Energy Technology Data Exchange (ETDEWEB)

    Chafetz, H.S.

    1990-04-30

    Bacteria induce the precipitation of calcium carbonate in the laboratory and in nature by altering their chemical environment. Geologists are recognizing the possibility that bacterially induced precipitates may form significant mineral deposits, unfortunately, there are currently no sound criteria by which they can be recognized in recent sediments, or in the rock record. Cultures of aerobic and facultative bacteria from cyanobacterial mats on Andros Island, Bahamas, and Baffin Bay, Texas, induced the precipitation of calcium carbonate under controlled conditions. Crusts, the largest features formed, are composed of 5--200{mu}m diameter bundles which are, in turn, composed of numerous individual crystals. The smallest observed features are 0.1--0.4{mu}m spheres and rods which comprise some individual crystals and crystal bundles. Crystal bundles resembling rhombohedra, tetragonal disphenoids, tetragonal dipyramids, and calcite dumbbells appear to be uniquely bacterial in origin, and they have all been observed in recent sediments. Swollen rods, discs, curved dumbbells, and 50--200{mu}m optically continuous crystals resembling brushes may be uniquely bacterial in origin, however, they have not been reported by other laboratories nor observed in natural settings. Presence of any of these forms in recent sediments should be taken as strong evidence for bacterial influence. Spheres and aragonite dumbbells have also been observed in natural environments, however, they are not always bacterial in origin. Precipitation of calcium carbonate occurs preferentially on dead cyanobacteria in the presence of bacteria. Lithification of algal mats to form stromatolites may take place in the zone of decaying organic matter due to bacterial activity.

  1. Crystal structure of N-[(methyl­sulfan­yl)carbon­yl]urea

    Science.gov (United States)

    Diop, Mouhamadou Birame; Diop, Libasse; Oliver, Allen G.

    2016-01-01

    The almost planar (r.m.s. deviation = 0.055 Å) title compound, (MeS)C(O)NHC(O)NH2, was formed during an attempted crystallization of dimethyl cyano­carbonimidodi­thio­ate with CrO2Cl2; an unexpected redox reaction converted the cyano­carbonimido moiety to a urea group and removed one methyl­thiol group. In the crystal, hydrogen-bonding inter­actions from the amide and amido N—H groups to carbonyl O atoms of neighbouring mol­ecules result in [010] ribbon-like chains. PMID:27006798

  2. Control of calcium carbonate crystallization by using anionic polymethylsiloxanes as templates

    Energy Technology Data Exchange (ETDEWEB)

    Neira-Carrillo, Andronico, E-mail: aneira@uchile.cl [Faculty of Veterinary and Animal Sciences, University of Chile, Santa Rosa 11735, PO Box 2-15, Santiago (Chile); Vasquez-Quitral, Patricio; Paz Diaz, Maria; Soledad Fernandez, Maria; Luis Arias, Jose [Faculty of Veterinary and Animal Sciences, University of Chile, Santa Rosa 11735, PO Box 2-15, Santiago (Chile); Yazdani-Pedram, Mehrdad [Faculty of Chemical and Pharmaceutical Science, University of Chile, S. Livingstone 1007, PO Box 233, Santiago (Chile)

    2012-10-15

    Sulfonated (SO{sub 3}H-PMS) and carboxylated (CO{sub 2}H-PMS) polymethylsiloxanes were synthesized and their effects as anionic template modifier on the CaCO{sub 3} crystal morphologies were evaluated. In vitro crystallization assays of CaCO{sub 3} were performed at room temperature by using gas diffusion method at different concentration, pH and time. SEM images of CaCO{sub 3} showed well-defined short calcite piles (ca. 5 {mu}m) and elongated calcite (ca. 20 {mu}m) when SO{sub 3}H-PMS was used. When CO{sub 2}H-PMS was used, the morphology of CaCO{sub 3} crystals was single-truncated at pH 7-9 and aggregated-modified calcite at pH 10-11. However, at pH 12 the least stable donut-shaped vaterite crystals were formed. EDS and XRD confirmed the presence of Si from anionic PMS templates on the CaCO{sub 3} surfaces and its polymorphism, respectively. Results showed that the selective morphologies of CaCO{sub 3} reflect the electrostatic interaction of anionic groups of functionalized PMS with Ca{sup 2+} adsorbed on CaCO{sub 3} crystals. Rounded and truncated-modified fluorescent CaCO{sub 3} was also produced by the inclusion of functionalized PMS into the lattice of CaCO{sub 3} matrix. We demonstrated that the anionic PMS offer a good modifier for polymer-controlled crystallization and a convenient approach for understanding the biomineralization field. - Graphical abstract: Optical photographs of rounded and truncated-modified fluorescent CaCO{sub 3} produced by the inclusion of sulfonated (SO{sub 3}H-PMS) polymethylsiloxanes into the lattice of CaCO{sub 3} matrix. Insert represents the simulation of modified and fluorescent CaCO{sub 3} crystals using Software JCrystal, (2008). Highlights: Black-Right-Pointing-Pointer We prepared two anionic polymethylsiloxanes (PMS) as templates. Black-Right-Pointing-Pointer Their modifier capacity on the CaCO{sub 3} crystal morphologies was demonstrated. Black-Right-Pointing-Pointer At pH 12, the least stable donut-shaped vaterite

  3. Crystal precipitation law of biodiesel based on thermodynamic phase equilibrium%利用热力学相平衡分析生物柴油晶体析出规律

    Institute of Scientific and Technical Information of China (English)

    梅德清; 谭文兵; 袁银男

    2013-01-01

      生物柴油主要是由饱和脂肪酸甲酯和不饱和脂肪酸甲酯组成的混合溶液,从热力学角度分析,生物柴油的蜡晶析出是溶液由液相向固相转变的相平衡过程。该文建立将液相组成作为理想溶液且固相成分不互溶的理想溶液模型(模型一)和基于活度系数模型与正规溶液理论的正规溶液模型(模型二),分别计算了蜡晶的析出温度,并且通过模型二计算出在给定的温度下的析蜡量与石蜡的组成。两模型在计算析蜡点的温度精确性方面还是比较理想的误差在5 K左右。研究发现石蜡沉积量与饱和脂肪酸酯的量成一定的比例关系,而且石蜡沉积并不是按照脂肪酸酯熔点高低的顺序进行析出,析出的石蜡中同时包含了低熔点脂肪酸酯。固液平衡常数是表征物质在溶液中析出能力的决定性因素,在一定温度下,不饱和脂肪酸酯的固液平衡常数一般在0.1以下,而饱和脂肪酸酯的固液平衡常数却大得多。该研究阐明的晶体析出规律,可为优化生物柴油低温流动性技术措施,推动生物柴油在低温环境下的应用提供参考。%Biodiesel, as a renewable alternative fuel with the virtue of clean burning, can be directly used in a diesel engine without any mechanic modification. However, biodiesel is easily crystallized at a low temperature, which limits the application of engines fueled with biodiesel, especially in severe cold circumstances. Biodiesel is a mixture solution, and mainly contains of saturated and unsaturated fatty acid methyl esters. According to thermodynamics, the process of wax precipitation is a thermodynamic equilibrium from liquid phase to solid phase. The equilibrium relationship between the solid phase and the liquid phase doesn’t keep constant. As long as one factor of the system changes, the phase diagram will follow changing. Two different kinds of models have been built to

  4. Lanthanide-activated Na{sub 5}Gd{sub 9}F{sub 32} nanocrystals precipitated from a borosilicate glass: Phase-separation-controlled crystallization and optical property

    Energy Technology Data Exchange (ETDEWEB)

    Chen, Daqin, E-mail: dqchen@hdu.edu.cn [College of Materials and Environmental Engineering, Hangzhou Dianzi University, Hangzhou 310018 (China); Key Laboratory of Design and Assembly of Functional Nanostructures, Fujian Institute of Research on the Structure of Matter, CAS, Fuzhou 350002 (China); Wan, Zhongyi; Zhou, Yang [College of Materials and Environmental Engineering, Hangzhou Dianzi University, Hangzhou 310018 (China); Chen, Yan, E-mail: chenyan@hdu.edu.cn [College of Materials and Environmental Engineering, Hangzhou Dianzi University, Hangzhou 310018 (China); Yu, Hua; Lu, Hongwei; Ji, Zhenguo [College of Materials and Environmental Engineering, Hangzhou Dianzi University, Hangzhou 310018 (China); Huang, Ping, E-mail: phuang@fjirsm.ac.cn [Key Laboratory of Design and Assembly of Functional Nanostructures, Fujian Institute of Research on the Structure of Matter, CAS, Fuzhou 350002 (China)

    2015-03-15

    Highlights: • Na{sub 5}Gd{sub 9}F{sub 32} nanocrystals embedded glass ceramics were fabricated for the first time. • Such glass ceramics were achieved by phase-separation-controlled crystallization. • Elemental mapping evidenced the segregation of activators into the Na{sub 5}Gd{sub 9}F{sub 32} lattice. • Luminescent color could be tuned by controlling glass crystallization temperature. - Abstract: Lanthanide-activated cubic Na{sub 5}Gd{sub 9}F{sub 32} nanocrystals were precipitated from a borosilicate glass with a specifically designed composition. The precursor glass is already phase-separated after melt-quenching, which is beneficial to the realization of the controllable glass crystallization for affording desirable size, morphology and activator partition. Elemental mapping in the scanning transmission electron microscopy evidenced that the segregation of lanthanide ions into the Na{sub 5}Gd{sub 9}F{sub 32} lattice was in situ formed without the requirement of long-range ionic diffusion. Impressively, such fabricated glass ceramic co-doped with Yb{sup 3+}/Er{sup 3+} ions exhibited intense upconversion luminescence, which was about 500 times higher than that of the precursor glass, and its luminescent color could be easily tuned from red to green by controlling glass crystallization temperature. It is anticipated that such phase-separation synthesis strategy with precise control over nanostructure of glass ceramics offer a great opportunity to design other highly transparent nanocomposites with a wide range of tunable optical properties.

  5. Mathematical model for Nb(C,N) precipitation kinetics in austenite controlled both by chemical and interfacial energy; Kaimen energy wo koryoshita {gamma} sochu deno Nb tanchikkabutsu no sekishutsu kyodo no teishikika

    Energy Technology Data Exchange (ETDEWEB)

    Okamoto, R.; Suehiro, M. [Nippon Steel Corp., Tokyo (Japan)

    1998-09-01

    A wide range of material characteristics can be obtained from steel materials by adjusting added elements and giving heat treatment. This is attributable to the fact that phase transformation, precipitation and re-crystallization of metallic structures can be combined and varied differently. Utilization of the precipitation phenomena may include strengthening of precipitation by using precipitates, structural control such as re-crystallization control by using precipitates, and making C, N and S harmless by forming them as precipitates. Individual precipitate grain sizes and effects of particle growth were incorporated into local equilibrium calculation using the model of Akamatsu et al for an attempt of structuring a model to estimate precipitation behavior from the beginning to the end by performing the calculation on each particle. Good reproduction was achieved on difference in precipitation behaviors of Nb (C, N) between a very low carbon component system and an HSLA component system having equal over-saturation degree as proved by experiments performed by Akamatsu et al. It has become possible to calculate precipitation behaviors of the precipitates all the way from the nucleation and growth process to the Ostwald growth process. It was also possible to evaluate grain size distribution of the precipitates, and present a characteristic grain size distribution provided by difference in driving force. Versatility and expandability of the model were increased by using the Thermo-Calc. 30 refs., 10 figs., 2 tabs.

  6. Space-Selective Precipitation of Ba2TiSi2O8 Crystals in Sm3+-Doped BaO-TiO2-SiO2 Glass by Femtosecond Laser Irradiation

    Institute of Scientific and Technical Information of China (English)

    ZHU Bin; DAI Ye; MA Hong-Liang; LIN Geng; QIU Jian-Rong

    2008-01-01

    The ferroelectric crystal Ba2TiSi2O8 with high second-order optical nonlinearity is precipitated in Sm3+-doped BaO-TiO2-SiO2 glass by a focused 800 nm,250 kHz and 150 fs femtosecond laser irradiation.No apparent blue and red emissions are observed at the beginning,while strong blue emission due to second harmonic generation and red emission due to the f-f transitions of Sm3+ are observed near the focal point of the laser beam after irradiation for 25 s. Micro-Raman spectra confirm that Ba2TiSi2O8 crystalline dots and lines are formed after laser irradiation.The mechanism of the phenomenon is discussed.

  7. Carbon exchange variability over Amazon Basin using coupledhydrometeorological-mixed layer PBL-carbon dioxide assimilation modeling system forced by satellite-derived surface radiation and precipitation

    Science.gov (United States)

    Grose, Andrew

    2004-12-01

    A hydrometeorological model is modified to include a simple slab model of the mixed layer for the estimation of CO2 fluxes in Amazonia. Three carbon assimilation models are examined for use in the FSU hydromet model, of which the NCAR LSM module is chosen because respiration rates are provided and CO2, latent and sensible heat fluxes are coupled through stomatal resistance. Initial calculations of NEP show a necessity for modeling canopy-boundary layer interactions to reproduce observed morning effluxes at forest tower sites at Manaus and Jaru. CO2 concentrations in five layers in and above the canopy are modeled with associated fluxes. Sensible heat fluxes are consistently overestimated until canopy heat capacity is taken into account. Estimations of canopy heat storage are found using observed differences between net incoming radiation and latent and sensible heat fluxes, or observed total residual energy. Calibration of fluxes at three tower sites is conducted using modeled total residual energy at the forest sites and modified photosynthesis parameters at the pasture site. The forcing parameters of downwelling solar radiation (K ↓) and temperature are found to exert the most influence over modeled CO2 fluxes at the tower sites. Model application over the basin shows that while vegetation type is the primary factor controlling CO2 fluxes area-wide, K ↓ is the primary forcing variable that produces spatial and temporal variability of CO2 fluxes. Modeled CO2 fluxes show mean monthly uptake values in the range of 1-3 mumol m-2 s-1 and diurnal progressions of large coherent areas of CO2 effluxes over the forest, progressing from SE to NW in December, and from NE to SW in June. Inspection of area-wide modeled fluxes near tower sites shows that the use of ECMWF winds and temperatures creates a spurious nocturnal stability that produces much larger morning efflux magnitudes than observations suggest. Comparison of CO2 fluxes at nearly 20,000 forest points within

  8. Influence of Purple Sulfur Bacteria on the biogeochemistry of Carbon and Sulfur Isotopes in Crystal Lake, OH

    Science.gov (United States)

    Meyer, A.; Nichols, D. L.; Cheng, S.

    2013-12-01

    Crystal Lakes are a series of four interconnected mesotrophic, moulin-induced glacial lakes in west-central Ohio. The study site, Main Lake (a.k.a. Crystal Lake), is the largest and deepest lake among them. It is about 5 ha with a maximum depth of 11.9 meters and a mean depth of 3.8 meters. Thermal stratification develops during the warmer months. Photosynthesis, which preferentially uptakes lighter isotopes, is the primary pathway for carbon and sulfur isotope fractionation in natural waters. Photosynthesizers present at Crystal Lake include green algae, diatoms, cyanobacteria, and purple sulfur bacteria (PSB). Phytoplankton growth is limited by nutrient availability, influencing the extent of fractionation. Purple sulfur bacteria (PSB) utilize sulfide as an electron donor instead of water. The layer of concentrated PSB population exists between oxic and anoxic water in lakes where sufficient light and sulfide are present. These bacteria impact the levels of several sulfur compounds and isotopic composition within lake systems by oxidizing sulfide to sulfate. Field parameters collected in warmer months show turbidity and chlorophyll peaks around 6 m with variations caused by temperature, light, and nutrient availability. The dissolved oxygen minimum and the redox and sulfate maxima generally correspond with the turbidity and chlorophyll peaks, indicating the presence of a PSB layer. This layer occurs at the boundary between the metalimnion and hypolimnion. Sulfide concentrations increased from a maximum of 0.02 mg/L in May to a maximum of 9.25 mg/L in August. In May sulfide was only found at 10.4 m and below while in August it was present at 6 m and below. Sulfate values remain relatively constant with a maximum at the layer of PSB, then decline with depth where Sulfide is abundant. δ13C-DIC values peak at 6 m corresponding with the layer of PSB. This peak may be due to the influence of PSB on carbon isotope fractionation. The carbon isotope composition of

  9. Struvite precipitation as a technology to be integrated in a manure anaerobic digestion treatment plant - removal efficiency, crystal characterization and agricultural assessment

    OpenAIRE

    Cerrillo Moreno, Miriam; Palatsi Civit, Jordi; Comas Angelet, Jordi; Bonmatí Blasi, August

    2015-01-01

    BACKGROUNDThe formation of struvite (MgNH4PO4 6H(2)O) from digested slurry is an opportunity to recover nutrients as a slow-release fertilizer. A series of batch and continuous experiments were conducted to assay the influence of operational parameters, total solids and organic matter content on the quality and size of struvite crystals formed. Finally, the agronomic bioavailability of struvite was assessed in a greenhouse experiment.; RESULTSIn terms of process conditions an optimum pH of 9 ...

  10. Crystallization of -type hexagonal ferrites from mechanically activated mixtures of barium carbonate and goethite

    Indian Academy of Sciences (India)

    J Temuujin; M Aoyama; M Senna; T Masuko; C Ando; H Kishi; A Minjigmaa

    2006-10-01

    -type hexagonal ferrite precursor was prepared by a soft mechanochemical treatment of BaCO3 and -FeOOH mixtures. The effect of milling on its structure and thermal behaviour was examined by XRD, SEM and FTIR. Well crystallized -type hexagonal ferrite was formed from just 1 h milled precursors at 800°C. The beneficial effect of milling was explained in terms of increased homogeneity with simultaneous hetero bridging bond formation between powder constituents.

  11. Production of biodiesel fuel from canola oil with dimethyl carbonate using an active sodium methoxide catalyst prepared by crystallization.

    Science.gov (United States)

    Kai, Takami; Mak, Goon Lum; Wada, Shohei; Nakazato, Tsutomu; Takanashi, Hirokazu; Uemura, Yoshimitsu

    2014-07-01

    In this study, a novel method for the production of biodiesel under mild conditions using fine particles of sodium methoxide formed in dimethyl carbonate (DMC) is proposed. Biodiesel is generally produced from vegetable oils by the transesterification of triglycerides with methanol. However, this reaction produces glycerol as a byproduct, and raw materials are not effectively utilized. Transesterification with DMC has recently been studied because glycerol is not formed in the process. Although solid-state sodium methoxide has been reported to be inactive for this reaction, the catalytic activity dramatically increased with the preparation of fine catalyst powders by crystallization. The transesterification of canola oil with DMC was studied using this catalyst for the preparation of biodiesel. A conversion greater than 96% was obtained at 65°C for 2h with a 3:1M ratio of DMC and oil and 2.0 wt% catalyst.

  12. Production of biodiesel fuel from canola oil with dimethyl carbonate using an active sodium methoxide catalyst prepared by crystallization.

    Science.gov (United States)

    Kai, Takami; Mak, Goon Lum; Wada, Shohei; Nakazato, Tsutomu; Takanashi, Hirokazu; Uemura, Yoshimitsu

    2014-07-01

    In this study, a novel method for the production of biodiesel under mild conditions using fine particles of sodium methoxide formed in dimethyl carbonate (DMC) is proposed. Biodiesel is generally produced from vegetable oils by the transesterification of triglycerides with methanol. However, this reaction produces glycerol as a byproduct, and raw materials are not effectively utilized. Transesterification with DMC has recently been studied because glycerol is not formed in the process. Although solid-state sodium methoxide has been reported to be inactive for this reaction, the catalytic activity dramatically increased with the preparation of fine catalyst powders by crystallization. The transesterification of canola oil with DMC was studied using this catalyst for the preparation of biodiesel. A conversion greater than 96% was obtained at 65°C for 2h with a 3:1M ratio of DMC and oil and 2.0 wt% catalyst. PMID:24813567

  13. Remarkable crystallization morphologies of poly(4-vinylpyridine on single-walled carbon nanotubes in CO2-expanded liquids

    Directory of Open Access Journals (Sweden)

    Y. N. Wei

    2011-12-01

    Full Text Available Poly(4-vinylpyridine (P4VP is a widely studied polymer for applications in catalysis, humidity sensitive and antimicrobial materials due to its pyridine group exhibiting coordinative reactivity with transition metals. In this work, the non-covalent functionalization of single-walled carbon nanotubes (SWCNTs with P4VP in CO2-expanded liquids (CXLs is reported. It is found that P4VP stabilized SWCNTs show good dispersion in both organic solvent and aqueous solution (pH = 2. The ability to manipulate the dispersion state of CNTs in water with P4VP will likely benefit many biological applications, such as drug delivery and optical sensors. Furthermore, the structure and morphology of P4VP/SWCNTs composite are examined, with the focus on molecular weight of P4VP (MW-P4VP, the pressure of CXLs and the concentration of P4VP. It is amazing that the P4VP15470 wrapping patterns undergo a notable morphological evolution from dotlike crystals to bottle brush-like, then to compact kebab-like, and then to widely-spaced dotted kebab patterns by facile pressure tuning in the higher polymer concentration series. In other words, the CXLs method enables superior control of the P4VP crystallization patterns on SWCNTs. Meanwhile, the CXL-assisted P4VP crystal growth mechanism on SWCNT is investigated, and the dominating growth mechanism is attributed to ‘size dependent soft epitaxy’ in P4VP15470/SWCNTs composites. We believe these studies would r

  14. On the Crystallization of Compacted and Chunky Graphite from Liquid Multicomponent Iron-Carbon-Silicon-Based Melts

    Science.gov (United States)

    Stefanescu, D. M.; Huff, R.; Alonso, G.; Larrañaga, P.; De la Fuente, E.; Suarez, R.

    2016-08-01

    Extensive SEM work was carried out on deep-etched specimens to reveal the evolution of compacted and chunky graphite in magnesium-modified multicomponent Fe-C-Si alloys during early solidification and at room temperature. The findings of this research were then integrated in the current body of knowledge to produce an understanding of the crystallization of compacted and chunky graphite. It was confirmed that growth from the liquid for both compacted and chunky graphite occurs radially from a nucleus, as foliated crystals and dendrites. The basic building blocks of the graphite aggregates are hexagonal faceted graphite platelets with nanometer height and micrometer width. Thickening of the platelets occurs through growth of additional graphene layers nucleated at the ledges of the graphite prism. Additional thickening resulting in complete joining of the platelets may occur from the recrystallization of the amorphous carbon that has diffused from the liquid through the austenite, once the graphite aggregate is enveloped in austenite. With increasing magnesium levels, the foliated graphite platelets progressively aggregate along the c-axis forming clusters. The clusters that have random orientation, eventually produce blocky graphite, as the spaces between the parallel platelets disappear. This is typical for compacted graphite irons and tadpole graphite. The chunky graphite aggregates investigated are conical sectors of graphite platelets stacked along the c-axis. The foliated dendrites that originally develop radially from a common nucleus may aggregate along the c-axis forming blocky graphite that sometimes exhibits helical growth. The large number of defects (cavities) observed in all graphite aggregates supports the mechanism of graphite growth as foliated crystals and dendrites.

  15. Experimental studies of the deformation of carbonated rocks by dissolution crystallization under stress

    International Nuclear Information System (INIS)

    The first part of this research thesis reports the experimental investigation and the modelling of the deformation of poly-mineral rocks under the influence of mechanism of dissolution-crystallization under stress. This mechanism has a significant role in the compaction of sedimentary rocks, in the folding process of the earth's crust. The author notably reports the results of the experimental deformation of calcite in presence of water (calcite is present in marls in which the deposit of nuclear wastes in planned in France). The second part deals with the fact that healing is possible between two grains of similar mineralogy, and slows down or even stops deformation

  16. Influence of the surfactant nature on the calcium carbonate synthesis in water-in-oil emulsion

    Science.gov (United States)

    Szcześ, Aleksandra

    2009-02-01

    Calcium carbonate has been precipitated from water-in-oil emulsions consisting of n-hexane/nonionic surfactant (Brij 30) and its mixture with cationic (DTAB) or anionic surfactant (SDS) to which calcium chloride and sodium carbonate were added. It was found that the surfactant kind and its amount can regulate the size, form and morphology of the precipitated particles. In case of nonionic surfactant the water/surfactant ratio is the most important parameter that allows to obtain small and regular calcium carbonate crystals. Addition of the DTAB results in different morphology of particles having the same crystal form, whereas addition of SDS changes the kind of emulsion from water-in-oil to oil-in-water. Moreover, light transmittance and backscattering light measurements have been used as a method to study the kinetics of calcium carbonate precipitation in emulsion systems.

  17. Protein Crystallization

    Science.gov (United States)

    Chernov, Alexander A.

    2005-01-01

    Nucleation, growth and perfection of protein crystals will be overviewed along with crystal mechanical properties. The knowledge is based on experiments using optical and force crystals behave similar to inorganic crystals, though with a difference in orders of magnitude in growing parameters. For example, the low incorporation rate of large biomolecules requires up to 100 times larger supersaturation to grow protein, rather than inorganic crystals. Nucleation is often poorly reproducible, partly because of turbulence accompanying the mixing of precipitant with protein solution. Light scattering reveals fluctuations of molecular cluster size, its growth, surface energies and increased clustering as protein ages. Growth most often occurs layer-by-layer resulting in faceted crystals. New molecular layer on crystal face is terminated by a step where molecular incorporation occurs. Quantitative data on the incorporation rate will be discussed. Rounded crystals with molecularly disordered interfaces will be explained. Defects in crystals compromise the x-ray diffraction resolution crucially needed to find the 3D atomic structure of biomolecules. The defects are immobile so that birth defects stay forever. All lattice defects known for inorganics are revealed in protein crystals. Contribution of molecular conformations to lattice disorder is important, but not studied. This contribution may be enhanced by stress field from other defects. Homologous impurities (e.g., dimers, acetylated molecules) are trapped more willingly by a growing crystal than foreign protein impurities. The trapped impurities induce internal stress eliminated in crystals exceeding a critical size (part of mni for ferritin, lysozyme). Lesser impurities are trapped from stagnant, as compared to the flowing, solution. Freezing may induce much more defects unless quickly amorphysizing intracrystalline water.

  18. Encodable multiple-fluorescence CdTe@carbon nanoparticles from nanocrystal/colloidal crystal guest-host ensembles

    Science.gov (United States)

    Guo, Xin; Wang, Cai-Feng; Mao, Li-Hua; Zhang, Jing; Yu, Zi-Yi; Chen, Su

    2013-04-01

    We report herein the controllable generation of encodable multi-fluorescence CdTe@carbon nanoparticles (CdTe@C NPs) via the pyrolysis of quantum dot/photonic crystal (QD/PC) guest-host ensembles. The precursors of CdTe/poly(styrene-co-glycidylmethacrylate) (PS-co-PGMA) QD/PC guest-host ensembles were initially formed via the assembly of epoxy groups of PCs and carboxyl groups on the surface of CdTe QDs, followed by a pyrolysis process to generate CdTe@C NPs. The as-prepared CdTe@C NPs not only integrate the optical properties for both the carbon and CdTe QD constituents, but also enable an impressive enhancement of the fluorescence lifetime for CdTe QDs. The multifarious fluorescent spectra coding for CdTe@C NPs was further generated through regulating the embedded sizes or concentrations of CdTe QDs and the excitation wavelength, and their applications in DNA detection and luminescent patterns were achieved.

  19. Synthesis, characterization and crystal structure of 1-ferrocenesulfonyl-2-1ong carbon chain alkyl benzimidazole

    Institute of Scientific and Technical Information of China (English)

    Junzhen ZHANG; Bingqin YANG; Yating YANG; Binglin ZHANG

    2009-01-01

    Six new 1-ferrocenesulfonyl-2-benzimidazole derivatives were prepared by the reaction of ferrocene-sulfonyl chloride with benzimidazole derivatives in the presence of dichloromethane and n-tetrabutylammonia bromide. The yields of these six new ferrocenesulfonyl benzimidazole derivatives were about 80%. The structures characteristic were confirmed by IR, 1H-NMR, Elemental analysis and MS. The crystal structure of compound a2 was determined via X-ray single crystal diffraction and it belongs to monoclinic system with space group C2/c,and the unit cell parameters are a=2.8252(2)nm, b=0.97696(7)nm, c=1.64828(12)nm, a=90°, β=92.053(2)°,y = 90°, V= 4.5466(6) nm3, Z= 8, F(000) =2024, Mr=481.40, Dc=l.407g/cm3, μ=0.784mm-1,R1=0.0495, wR2=0.1517. The results show that the reactions of 2-alkylbenzimidazoles containing active hydrogen with ferrocenesulfonyl chloride gave 1-ferrocenesulfonyl-2-alkylbenzimidazoles in good yields.

  20. Crystal structure and kinetic studies of a tetrameric type II β-carbonic anhydrase from the pathogenic bacterium Vibrio cholerae.

    Science.gov (United States)

    Ferraroni, Marta; Del Prete, Sonia; Vullo, Daniela; Capasso, Clemente; Supuran, Claudiu T

    2015-12-01

    Carbonic anhydrase (CA) is a zinc enzyme that catalyzes the reversible conversion of carbon dioxide to bicarbonate (hydrogen carbonate) and a proton. CAs have been extensively investigated owing to their involvement in numerous physiological and pathological processes. Currently, CA inhibitors are widely used as antiglaucoma, anticancer and anti-obesity drugs and for the treatment of neurological disorders. Recently, the potential use of CA inhibitors to fight infections caused by protozoa, fungi and bacteria has emerged as a new research direction. In this article, the cloning and kinetic characterization of the β-CA from Vibrio cholerae (VchCAβ) are reported. The X-ray crystal structure of this new enzyme was solved at 1.9 Å resolution from a crystal that was perfectly merohedrally twinned, revealing a tetrameric type II β-CA with a closed active site in which the zinc is tetrahedrally coordinated to Cys42, Asp44, His98 and Cys101. The substrate bicarbonate was found bound in a noncatalytic binding pocket close to the zinc ion, as reported for a few other β-CAs, such as those from Escherichia coli and Haemophilus influenzae. At pH 8.3, the enzyme showed a significant catalytic activity for the physiological reaction of the hydration of CO2 to bicarbonate and protons, with the following kinetic parameters: a kcat of 3.34 × 10(5) s(-1) and a kcat/Km of 4.1 × 10(7) M(-1) s(-1). The new enzyme, on the other hand, was poorly inhibited by acetazolamide (Ki of 4.5 µM). As this bacterial pathogen encodes at least three CAs, an α-CA, a β-CA and a γ-CA, these enzymes probably play an important role in the life cycle and pathogenicity of Vibrio, and it cannot be excluded that interference with their activity may be exploited therapeutically to obtain antibiotics with a different mechanism of action.

  1. Carbon-based micro-ball and micro-crystal deposition using filamentary pulsed atmospheric pressure plasma

    International Nuclear Information System (INIS)

    Thin plasma filaments are produced by the propagation of ionization waves from a spiked driven electrode in a quartz tube in an argon/methane gas mixture (2400 sccm/2 sccm) at atmospheric pressure. The position of the touch point of filaments on the substrate surface is controlled in our experiment by applying various suitable substrate configurations and geometries of the grounded electrode. The gas conditions at the touch point are varied from argon to ambient air. Based on microphotography and discharge current waveforms, the duration of the filament touching the substrate is estimated to be about one microsecond. Carbon-based materials are deposited during this time at the touch points on the substrate surface. Micro-balls are produced if the filament touch points are saved from ambient air by the argon flow. Under an air admixture, micro-crystals are formed. The dimension of both materials is approximately one micrometre (0.5–2 µm) and corresponds to about 1010–1012 carbon atoms. Neither the diffusion of neutral species nor drift of ions can be reason for the formation of such a big micro-material during this short period of filament–substrate interaction. It is possible that charged carbon-based materials are formed in the plasma channel and transported to the surface of the substrate. The mechanism of this transport and characterization of micro-materials, which are formed under different gas conditions in our experiment, will be studied in the future. (paper)

  2. Phosphate recovery through struvite precipitation by CO{sub 2} removal: Effect of magnesium, phosphate and ammonium concentrations

    Energy Technology Data Exchange (ETDEWEB)

    Korchef, Atef, E-mail: atef.korchef@inrst.rnrt.tn [Centre of Waters Researches and Technologies, Technopark of Borj-Cedria, CERTE, BP 273, Soliman 8020 (Tunisia); Saidou, Hassidou; Amor, Mohamed Ben [Centre of Waters Researches and Technologies, Technopark of Borj-Cedria, CERTE, BP 273, Soliman 8020 (Tunisia)

    2011-02-15

    In the present study, the precipitation of struvite (MgNH{sub 4}PO{sub 4}.6H{sub 2}O) using the CO{sub 2} degasification technique is investigated. The precipitation of struvite was done from supersaturated solutions in which precipitation was induced by the increase of the solution supersaturation concomitant with the removal of dissolved carbon dioxide. The effect of magnesium, phosphate and ammonium concentrations on the kinetics and the efficiency of struvite precipitation was measured monitoring the respective concentrations in solution. In all cases struvite precipitated exclusively and the solid was characterized by powder XRD and FTIR. The morphology of the precipitated crystals was examined by scanning electronic microscopy and it was found that it exhibited the typical prismatic pattern of the struvite crystals with sizes in the range between 100 and 300 {mu}m. The increase of magnesium concentration in the supersaturated solutions, resulted for all phosphate concentration tested, in significantly higher phosphate removal efficiency. Moreover, it is interesting to note that in this case the adhesion of the suspended struvite crystals to the reactor walls was reduced suggesting changes in the particle characteristics. The increase of phosphate concentration in the supersaturated solutions, for the magnesium concentrations tested resulted to the reduction of struvite suppression which reached complete suppression of the precipitate formation. Excess of ammonium in solution was found favour struvite precipitation. Contrary to the results found with increasing the magnesium concentration in solution, higher ammonium concentrations resulted to higher adhesion of the precipitated crystallites to the reactor walls. The results of the present work showed that it is possible to recover phosphorus in the form of struvite from wastewater reducing water pollution and at the same time saving valuable resources.

  3. Computer simulation of channelling measurements in carbon-implanted NbC-single crystals

    International Nuclear Information System (INIS)

    A Monte-Carlo-program has been used to study the channelling process in NbC-single crystals implanted with C-ions at 8300C. The dechannelling yields measured in the -direction separately for the Nb- and the C-sublattice are compared to calculated results. In the calculation two defect models (statistically displaced C-atoms and stacking faults) were applied and the characteristic parameters for these models were varied in order to reproduce the behavior of the experimental spectra. The best agreement was obtained by assuming a defect structure consisting of stacking faults with a Burger's vector of a6 [112] and a stacking fault length of 7 nm. The analyzing ion beam energy was varied in the calculation and the expected energy independence of the dechannelling yield for stacking faults was found which lies in reasonable agreement with the experimental values. (orig.)

  4. Stress from NaCl crystallization by CO2 injection in aquifers

    OpenAIRE

    Osselin, Florian; Fabbri, Antonin; FEN CHONG, Teddy; Dangla, Patrick; Pereira, Jean-Michel; Lassin, Arnault

    2015-01-01

    The goal of this paper is to identify the mechanical impact of water evaporation and salt crystallisation during supercritical carbon dioxide injection (drying-out process) in aquifer rocks. The precipitation of salt and the resulting crystallisation pressure are inferred from the chemical equilibrium of the carbon dioxide-rich gas phase, the in-pore brine and the crystal. The induced rock strain and equivalent tensile stress are then estimated within the framework of isotropic linear poroela...

  5. Preparation of Nano-hexagonal Plate Mg-Al Water Talc Crystal Through Co-precipitation%纳米六角片状镁铝水滑石晶体的共沉淀法制备

    Institute of Scientific and Technical Information of China (English)

    陈利花; 梁小平

    2012-01-01

    以共沉淀法制备镁铝水滑石,主要研究了原料物质的量浓度和反应温度等参数对纳米晶的影响.采用透射电镜(TEM)、X线衍射(XRD)仪等对纳米晶进行表征.结果表明采用共沉淀法可制备出纯相六角片状结构的纳米镁铝水滑石晶体.制备工艺条件为NaOH物质的量浓度大于0.625mol/L、反应温度90℃、Na2CO3物质的量浓度为0.09mol/L时镁铝水滑石产率可达到最大值95%.%The study is set on the preparation of magnesium aluminates water talc with co-precipitation method, focusing on the influence of raw material concentration and reaction temperature parameters on nanocrystalline. The methods of scanning electron microscope (TEM), X-ray Diffract(XRD) meter and other methods were used to characterize Nanocrystalline. The results show that pure phase structure of the nana magnesium hex flake aluminum water talc crystals can be prepared with the use of co-precipitation. The best preparation conditions are: NaOH concentration over 0. 625 mol/L, reaction temperature 90 ℃ , Na2CO3 concentration of 0.09 mol/L. The yield of magnesium aluminates water talc will reach a maximumof 95%.

  6. Crystal structure of polymeric carbon nitride and the determination of its process-temperature-induced modifications

    Science.gov (United States)

    Tyborski, T.; Merschjann, C.; Orthmann, S.; Yang, F.; Lux-Steiner, M.-Ch; Schedel-Niedrig, Th

    2013-10-01

    Based on the arrangement of two-dimensional ‘melon’, we construct a unit cell for polymeric carbon nitride (PCN) synthesized via thermal polycondensation, whose theoretical diffraction powder pattern includes all major features measured in x-ray diffraction. With the help of this unit cell, we describe the process-temperature-induced crystallographic changes in PCN that occur within a temperature interval between 510 and 610 °C. We also discuss further potential modifications of the unit cell for PCN. It is found that both triazine- and heptazine-based g-C3N4 can only account for minor phases within the investigated synthesis products.

  7. Precipitation kinetics of a continuous precipitator, with application to the precipitation of ammonium polyuranate

    International Nuclear Information System (INIS)

    A mathematical model describing the kinetics of continuous precipitation was developed which accounts for crystal nucleation, crystal growth, primary coagulation, and secondary coagulation. Population density distributions, average particle sizes, dominant particle sizes, and suspension density fractions of the crystallites, primary agglomerates, and secondary agglomerates leaving the continuous precipitator can be determined. This kinetic model was applied to the continuous precipitation of ammonium polyuranate, which consists of: (1) elementary crystals, (2) clusters or primary coagulated particles, and (3) agglomerates or secondary coagulated particles. The crystallites are thin, submicron, hexagonal platelets. The clusters had an upper size limit of about 7 μ in diameter and contained numerous small voids (less than 0.3 μm) due to the packing of the crystallites. The agglomerates had an upper size limit of about 40 μm in diameter and contained large voids (approximately 1 μm). The particle size distribution and particle structure of the ammonium polyuranate precipitate can be controlled through proper regulation of the precipitation conditions. The ratio of clusters to agglomerates can be best controlled through the uranium concentration, and the cohesiveness or internal bonding strength of the particles can be controlled with the ammonium to uranium reacting feed mole ratio. These two conditions, in conjunction with the residence time, will determine the nucleation rates, growth rates, and size distributions of the particles leaving the continuous precipitator. With proper control of these physical particle characteristics, the use of pore formers, ball-milling, and powder blending can probably be eliminated from the nuclear fuel fabrication process, substantially reducing the cost

  8. Bacterially induced precipitation of CaCO{sub 3}: An example from studies of cyanobacterial mats. Final report

    Energy Technology Data Exchange (ETDEWEB)

    Chafetz, H.S.

    1990-04-30

    Bacteria induce the precipitation of calcium carbonate in the laboratory and in nature by altering their chemical environment. Geologists are recognizing the possibility that bacterially induced precipitates may form significant mineral deposits, unfortunately, there are currently no sound criteria by which they can be recognized in recent sediments, or in the rock record. Cultures of aerobic and facultative bacteria from cyanobacterial mats on Andros Island, Bahamas, and Baffin Bay, Texas, induced the precipitation of calcium carbonate under controlled conditions. Crusts, the largest features formed, are composed of 5--200{mu}m diameter bundles which are, in turn, composed of numerous individual crystals. The smallest observed features are 0.1--0.4{mu}m spheres and rods which comprise some individual crystals and crystal bundles. Crystal bundles resembling rhombohedra, tetragonal disphenoids, tetragonal dipyramids, and calcite dumbbells appear to be uniquely bacterial in origin, and they have all been observed in recent sediments. Swollen rods, discs, curved dumbbells, and 50--200{mu}m optically continuous crystals resembling brushes may be uniquely bacterial in origin, however, they have not been reported by other laboratories nor observed in natural settings. Presence of any of these forms in recent sediments should be taken as strong evidence for bacterial influence. Spheres and aragonite dumbbells have also been observed in natural environments, however, they are not always bacterial in origin. Precipitation of calcium carbonate occurs preferentially on dead cyanobacteria in the presence of bacteria. Lithification of algal mats to form stromatolites may take place in the zone of decaying organic matter due to bacterial activity.

  9. Interactive effects of belowground organic matter input, increased precipitation and clipping on soil carbon and nitrogen mineralization in a temperate steppe

    Directory of Open Access Journals (Sweden)

    L. N. Ma

    2013-06-01

    Full Text Available Soil organic matter (SOM inputs, increased precipitation and clipping (reducing belowground photosynthates allocation are predicted to affect soil C and N cycling in temperate grassland ecosystems. However, the interactive effects between SOM inputs (or increased precipitation and clipping on soil C and N mineralization in temperate steppes are still poorly understood. A field manipulation experiment was conducted to quantify the effects of SOM inputs, increased precipitation, clipping and their interactions on soil C and N mineralization in a temperate steppe of northeastern China from 2010 to 2011. The results showed that SOM inputs significantly increased soil C mineralization rate (CMR and net N mineralization rate (NMR. Increased precipitation-induced enhancement of soil CMR essentially ceased after the first year, stimulation of soil NMR and NNR continued into the second year. However, clipping only marginally decreased soil CMR and NMR during the two years. There were significant synergistic interactions between SOM inputs (or increased precipitation and clipping on soil CMR and NMR, as SOM inputs (or increased precipitation showed greater effects on soil CMR and NMR under clipped plots than under unclipped plots, which could be explained by the relative shifts in soil microbial community structure because of bacterial biomass increases, and by the relative decreases in arbuscular mycorrhizal fungi biomass due to the reduction of belowground photosynthates allocation. These results highlight the importance of plants in mediating the responses of soil C and N mineralization to potentially increased SOM and precipitation by controlling belowground photosynthates allocation in the temperate steppe. Thus, the findings have important implications for improving prediction of C and N sequestration potential and its feedbacks to climate change in temperate steppe ecosystems.

  10. Tailoring polyacrylonitrile interfacial morphological structure by crystallization in the presence of single-wall carbon nanotubes.

    Science.gov (United States)

    Zhang, Yiying; Song, Kenan; Meng, Jiangsha; Minus, Marilyn L

    2013-02-01

    In order to improve stress transfer between polymer matrixes and nanofillers, controlling the structure development in the interphase region during composite processing is a necessity. For polyacrylonitrile (PAN)/single-wall carbon nanotubes (SWNT) composites, the formation of the PAN interphase in the presence of the SWNT as a function of processing conditions is studied. Under these conditions, three distinct interfacial coating morphologies of PAN are observed on SWNT. In the semidilute polymer concentration regime subjected to shearing, PAN extended-chain tubular coatings are formed on SWNT. Dilute PAN/SWNT quiescent solutions subjected to cooling yields hybrid periodic shish-kebab structures (first observation for PAN polymer), and dilute PAN/SWNT quiescent solutions subjected to rapid cooling results in the formation of an irregular PAN crystalline coating on the SWNT. PMID:23286387

  11. Modeling Carbon Sequestration over the Large-Scale Amazon Basin, Aided by Satellite Observations. Part I: Wet- and Dry-Season Surface Radiation Budget Flux and Precipitation Variability Based on GOES Retrievals.

    Science.gov (United States)

    Gu, Jiujing; Smith, Eric A.; Cooper, Harry J.; Grose, Andrew; Liu, Guosheng; Merritt, James D.; Waterloo, Maarten J.; de Araújo, Alessandro C.; Nobre, Antonio D.; Manzi, Antonio O.; Marengo, Jose; de Oliveira, Paulo J.; von Randow, Celso; Norman, John; Silva Dias, Pedro

    2004-06-01

    In this first part of a two-part investigation, large-scale Geostationary Operational Environmental Satellite (GOES) analyses over the Amazônia region have been carried out for March and October of 1999 to provide detailed information on surface radiation budget (SRB) and precipitation variability. SRB fluxes and rainfall are the two foremost cloud-modulated control variables that affect land surface processes, and they require specification at space time resolutions concomitant with the changing cloud field to represent adequately the complex coupling of energy, water, and carbon budgets. These processes ultimately determine the relative variations in carbon sequestration and carbon dioxide release within a forest ecosystem. SRB and precipitation retrieval algorithms using GOES imager measurements are used to retrieve surface downward radiation and surface rain rates at high space time resolutions for large-scale carbon budget modeling applications in conjunction with the Large-Scale Biosphere Atmosphere Experiment in Amazônia. To validate the retrieval algorithms, instantaneous estimates of SRB fluxes and rain rates over 8 km × 8 km areas were compared with 30-min-averaged surface measurements obtained from tower sites located near Ji-Paraná and Manaus in the states of Rondônia and Amazonas, respectively. Because of large aerosol concentrations originating from biomass burning during the dry season (i.e., September and October for purposes of this analysis), an aerosol index from the Total Ozone Mapping Spectrometer is used in the solar radiation retrieval algorithm. The validation comparisons indicate that bias errors for incoming total solar, photosynthetically active radiation (PAR), and infrared flux retrievals are under 4%, 6%, and 3% of the mean values, respectively. Precision errors at the analyzed space time scales are on the order of 20%, 20%, and 5%. The visible and infrared satellite measurements used for precipitation retrieval do not directly

  12. Calcium carbonate precipitation by heterotrophic bacteria isolated from biofilms formed on deteriorated ignimbrite stones: influence of calcium on EPS production and biofilm formation by these isolates.

    Science.gov (United States)

    López-Moreno, Angélica; Sepúlveda-Sánchez, José David; Mercedes Alonso Guzmán, Elia Mercedes; Le Borgne, Sylvie

    2014-01-01

    Heterotrophic CaCO3-precipitating bacteria were isolated from biofilms on deteriorated ignimbrites, siliceous acidic rocks, from Morelia Cathedral (Mexico) and identified as Enterobacter cancerogenus (22e), Bacillus sp. (32a) and Bacillus subtilis (52g). In solid medium, 22e and 32a precipitated calcite and vaterite while 52g produced calcite. Urease activity was detected in these isolates and CaCO3 precipitation increased in the presence of urea in the liquid medium. In the presence of calcium, EPS production decreased in 22e and 32a and increased in 52g. Under laboratory conditions, ignimbrite colonization by these isolates only occurred in the presence of calcium and no CaCO3 was precipitated. Calcium may therefore be important for biofilm formation on stones. The importance of the type of stone, here a siliceous stone, on biological colonization is emphasized. This calcium effect has not been reported on calcareous materials. The importance of the effect of calcium on EPS production and biofilm formation is discussed in relation to other applications of CaCO3 precipitation by bacteria.

  13. Detailed crystallization study of co-precipitated Y{sub 1.47} Gd{sub 1.53} Fe{sub 5} O{sub 12} and relevant magnetic properties

    Energy Technology Data Exchange (ETDEWEB)

    Serra, Rogerio Arving [Instituto de Criminalistica Carlos Eboli (ICCE), Rio de Janeiro, RJ (Brazil); Ogasawara, Tsuneharu; Ogasawara, Angelica Soares [Universidade Federal do Rio de Janeiro (UFRJ), RJ (Brazil). Coordenacao dos Programas de Pos-graduacao de Engenharia (COPPE). Dept. de Engenharia Metalurgica e de Materiais]. E-mail: ogasawat@metalmat.ufrj.br

    2007-07-01

    The crystallization process of co-precipitated Y{sub 1.5}Gd{sub 1.5}Fe{sub 5}O{sub 12} powder heated up to 1000 deg C at rate of 5 deg C min{sup -1} was investigated. Above 810 deg C crystalline Y{sub 1.47}Gd{sub 1.53}Fe{sub 5}O{sub 12} was obtained with a lattice parameter of 12.41 A and a theoretical density of 5.84 g cm{sup -3}. Dry pressed rings were sintered at 1270 and 1320 deg C, increasing the grain-size from 3.1 to 6.5 {mu}m, the theoretical density by 87.6 to 95.3% and decreasing H{sub c} from 2.9725 to 1.4005 Oe. Additionally, Hc increased when the frequency of the hysteresis graph varied from 60 Hz to 10 kHz, the curie temperature was 282.4 deg C and Ms equalled 9.25 emu g{sup -1} (0.17 kG) agreeing well with the B{sub s}-value of the hysteresis graph and literature values. (author)

  14. Asynchronous evolution of the isotopic composition and amount of precipitation in north China during the Holocene revealed by a record of compound-specific carbon and hydrogen isotopes of long-chain n-alkanes from an alpine lake

    Science.gov (United States)

    Rao, Zhiguo; Jia, Guodong; Li, Yunxia; Chen, Jianhui; Xu, Qinghai; Chen, Fahu

    2016-07-01

    Both the timing of the maximum East Asian summer monsoon (EASM) intensity in monsoonal China and the environmental significance of the Chinese stalagmite oxygen isotopic record (δ18O) have been debated. Here, we present a ca. 120-year-resolution compound-specific carbon (δ13C) and hydrogen (δD) isotopes of terrestrial long-chain n-alkanes extracted from a well-dated sediment core from an alpine lake in north China. Our δ13C data, together with previously reported pollen data from a parallel core, demonstrate a humid mid-Holocene from ca. 8-5 ka BP. Assuming that the climatic humidity of north China is an indicator of the EASM intensity, then the maximum EASM intensity occurred in the mid-Holocene. Our δD data reveal a similar long-term trend to the δ18O record from nearby Lianhua Cave, indicating that the synchronous δD and δ18O records faithfully record the δD and δ18O of precipitation, respectively. The most negative δD and δ18O values occur in the early-mid Holocene, from ca. 11-5 ka BP. This contrast in the timing of isotopic variations demonstrates a complex relationship between the isotopic composition of precipitation and precipitation amount, or EASM intensity. Further comparisons indicate a possible linkage between the precipitation amount in north China and the west-east thermal gradient in the equatorial Pacific. In addition, the temperature of the moisture source area may play an important role in determining the isotopic composition of precipitation in monsoonal China.

  15. Effects of carbon nanotubes on liquid crystal order parameter and Freedericksz transition in electro-optic cells

    Science.gov (United States)

    Georgiev, Georgi; Gombos, Erin; McIntyre, Michael; Mattera, Michael; Gati, Peter; Cabrera, Yaniel; Cebe, Peggy

    2010-03-01

    We studied the effects of multiwalled carbon nanotubes (MWCTs) at low concentrations (0.01 wt %) on the Freedericksz transition of a 4-Cyano-4'-pentylbipenyl (5CB) liquid crystal using transmission ellipsometry. In addition, we calibrated the altitudinal angle of CNTs as a function of the electric field and directed the azimuthal angle which gave us complete control of the 3D orientation of the CNTs. Our results show that in the presence of CNTs the voltage and width for the Freedericksz transition are reduced by a factor of 1.8 as compared to the control electro-optic cell without CNTs. The shift in transition voltage correlates with increase in order parameter of the electro-optic cell as measured by our polarized UV/Vis absorption spectroscopy results. Research supported by: Assumption College Faculty Development Grant, funding for students' stipends, instrumentation and supplies, the NSF Polymers Program of the DME, grant (DMR-0602473) and NASA grant (NAG8-1167).

  16. Chemical precipitation for controlling nitrogen loss during composting.

    Science.gov (United States)

    Ren, Li-Mei; Li, Guo-Xue; Shen, Yun-Jun; Schuchardt, Frank; Lu Peng

    2010-05-01

    Aimed at controlling the nitrogen loss during composting, the mixture of magnesium hydroxide (Mg(OH)( 2)) and phosphoric acid (H(3)PO(4)) (molar ratio 1:2) were utilized as additives to avoid increasing total salinity. In trial TA, the additives were put into absorption bottles connecting with a gas outlet of fermentor (ex situ method); in trial TB, the additives were directly added to the composting materials (in situ method). During the 26 day composting period, the temperature, pH, total organic carbon (TOC), total nitrogen (TN), ammonium nitrogen (NH(4)(+)-N), total phosphorus (TP), available phosphorus (AP) and germination index (GI) were measured. The experimental results show that the additives reduced the pH, while NH( 4)(+)-N and TN were obviously improved. NH(4)( +)-N was 11.9 g kg(-1) and 3 g kg(- 1) in amended compost trial (TB) and unamended compost trial (TA), respectively; TN increased from 26.5 g kg(-1) to 40.3 g kg(-1) in TB and increased from 26.5 g kg( -1) to 26.8 g kg(-1) in TA. Analysis of the TOC and carbon mass revealed that absorbents accelerated the degradation of organic matter. The germination index test showed the maturity of TB (102%) was better than TA (82%) in final compost. Furthermore, TP and AP were also obviously improved. X-ray diffraction analysis of precipitation showed that the precipitation in absorption bottle of TA was newberyite (MgHPO( 4) 3H(2)O), however, the crystal in the TB compost was struvite (MgNH(4)PO(4) 6H(2)O: magnesium ammonium phosphate). These results indicated that Mg(OH)(2) and H(3)PO( 4) could reduce the ammonia emission by struvite crystallization reaction. Optimal conditions for struvite precipitation should be determined for different systems. PMID:19808738

  17. 单晶高温合金DD6再结晶晶界析出相特征及其形成机制%CHARACTERISTIC AND FORMATION MECHANISM OF PRECIPITATES AT RECRYSTALLIZATION GRAIN BOUNDARIES OF SINGLE CRYSTAL SUPERALLOY DD6

    Institute of Scientific and Technical Information of China (English)

    熊继春; 李嘉荣; 赵金乾; 刘世忠; 董建新

    2009-01-01

    Single crystal superalloys have extremely good elevated temperature capability in advanced gas turbine aero engines due to no highly stressed grain boundaries in them. With the removal of grain boundary strengthening elements such as C, B and Zr, the occurrence of recrystallization may be detrimental to their performance. Therefore, recrystallization becomes critical in industrial manufacture of single crystal superalloy blades. In the present study, specimens of single crystal superalloy DD6 were grit blasted, solution treated and aged at vacuum atmosphere, and then the precipitates at recrystallization grain boundaries were investigated by SEM, TEM, EPMA and Thermo-Calc. The results show that a few of M_6C carbides precipitate at recrystallization grain boundaries, and their size is about 0.5 μm. These M_6C carbides are rich in W, Re and Mo, but poor in Al, Ta, Ni, the contents of Cr, Nb, Co in them are almost the same as the nominal composition of DD6 alloy. The carbon accumulation at recrystallization boundaries and combination with μ phase forming elements such as W and Mo restrain the μ phase forming. M_(23)C_6 phase hardly forms in DD6 alloy due to its high W and low Cr content.%对单晶高温合金DD6进行表面吹砂处理,然后进行固溶与时效真空热处理,采用SEM,TEM,EPMA和Thermo-Calc的方法研究了单晶合金DD6再结晶晶界析出相的特征及其形成机制.结果表明,经过吹砂处理的DD6合金在固溶与时效热处理过程中发生再结晶.再结晶晶界出现析出相,分析表明析出相为M6C碳化物,该碳化物呈粒状析出,尺寸约为0.5 μm,数量极少,富含W,Re和Mo,且Cr,Nb和Co的含量与合金名义成分差别不大,而Al,Ta和Ni含量较低.由于再结晶晶界上C元素的聚集效应,C原子在晶界上达到一定浓度后即与一定数量的W,Mo等μ相形成元素发生相变反应,抑制了合金析出μ相的倾向.又因为DD6合金W含量较高,而Cr含量较低,抑制了M_(23)C_6

  18. Mineral Carbonation Employing Ultramafic Mine Waste

    Science.gov (United States)

    Southam, G.; McCutcheon, J.; Power, I. M.; Harrison, A. L.; Wilson, S. A.; Dipple, G. M.

    2014-12-01

    Carbonate minerals are an important, stable carbon sink being investigated as a strategy to sequester CO2 produced by human activity. A natural playa (Atlin, BC, CAN) that has demonstrated the ability to microbially-accelerate hydromagnesite formation was used as an experimental model. Growth of microbial mats from Atlin, in a 10 m long flow-through bioreactor catalysed hydromagnesite precipitation under 'natural' conditions. To enhance mineral carbonation, chrysotile from the Clinton Creek Asbestos Mine (YT, CAN) was used as a target substrate for sulphuric acid leaching, releasing as much as 94% of the magnesium into solution via chemical weathering. This magnesium-rich 'feedstock' was used to examine the ability of the microbialites to enhance carbonate mineral precipitation using only atmospheric CO2 as the carbon source. The phototrophic consortium catalysed the precipitation of platy hydromagnesite [Mg5(CO3)4(OH)2·4H2O] accompanied by magnesite [MgCO3], aragonite [CaCO3], and minor dypingite [Mg5(CO3)4(OH)2·5H2O]. Scanning Electron Microscopy-Energy Dispersive Spectroscopy indicated that cell exteriors and extracellular polymeric substances (EPS) served as nucleation sites for carbonate precipitation. In many cases, entire cyanobacteria filaments were entombed in magnesium carbonate coatings, which appeared to contain a framework of EPS. Cell coatings were composed of small crystals, which intuitively resulted from rapid crystal nucleation. Excess nutrient addition generated eutrophic conditions in the bioreactor, resulting in the growth of a pellicle that sealed the bioreactor contents from the atmosphere. The resulting anaerobic conditions induced fermentation and subsequent acid generation, which in turn caused a drop in pH to circumneutral values and a reduction in carbonate precipitation. Monitoring of the water chemistry conditions indicated that a high pH (> 9.4), and relatively high concentrations of magnesium (> 3000 ppm), compared with the natural

  19. 一种单晶高温合金中γ'相的析出行为%The Precipitation of γ'-phase in a Single Crystal Superalloy

    Institute of Scientific and Technical Information of China (English)

    杨旭

    2011-01-01

    研究了固溶冷却速度和时效时间对一种镍基单晶高温合金中γ'相的析出的影响.合金经1250℃固溶处理4 h.从炉中快速取出,分别进行空冷、油冷和水冷,以考察冷却速度对γ'相析出的影响.随后对固溶处理后试样进行时效处理,以考察时效时问和固溶冷却速度对γ'相长大的影响.结果表明,合金在固溶处理后,γ'相尺寸随固溶冷却速率的升高而下降.在时效处理时,γ'相尺寸的增大率随固溶冷却速度的增大而减小;随着时效时间的增加,γ'相的尺寸增加.%The effects of cooling rate and aging time on the precipitation of ,γ'-phase in a single crystal superalloy were studied. The superalloy was cooled in air, oil and water after solution heat treatment at 1 250 ℃ for 4hours ,respectively, to study the effect of cooling rate on the precipitation of γ'-phase. The solution treated samples were aging treated at 850 ℃ for 24 hours to study the effects of cooling rate and aging time on the growth of γ'-phase. The experiment results show that the size of γ'-phase decreases with the increase of cooling rate during the process of cooling. During the aging process, the size enhancement coefficient of γ'-phase increases as cooling rate decreases, and the size of γ'-phase increases with the increase of aging time.

  20. Final report for grant number DE-FG02-06ER64244 to the University of Idaho (RW Smith)-coupling between flow and precipitation in heterogeneous subsurface environments and effects on contaminant fate and transport

    Energy Technology Data Exchange (ETDEWEB)

    Smith, Robert W. [Univ. of Idaho, Idaho Falls, ID (United States); Beig, Mikala S. [Univ. of Idaho, Idaho Falls, ID (United States); Gebrehiwet, Tsigabu [Univ. of Idaho, Idaho Falls, ID (United States); Corriveau, Catherine E. [Univ. of Idaho, Idaho Falls, ID (United States); Redden, George [Idaho National Lab. (INL), Idaho Falls, ID (United States); Fujita, Yoshiko [Idaho National Lab. (INL), Idaho Falls, ID (United States)

    2010-06-18

    Engineered remediation strategies for inducing mineral precipitation in the subsurface typically involve the introduction of at least one reactant either by direct injection or by in situ generation. The localization of reactant sources means a wide range of saturation states and ion ratios will be created as reactants are mixed: These conditions together can result in a wide range of precipitation rates, as well as impact which mineral phase precipitates. This is potentially important for the capacity of the precipitates to take up of trace metal contaminants, for their long term stability. Aragonite, for example, is able to sequester a larger amount of Sr than calcite. However, aragonite is less stable under typical groundwater conditions, and so may release sequestered Sr over time as the aragonite transforms to a more stable phase. In addition, previous experimental studies have indicated that other system constituents may influence calcium carbonate precipitation and consequently the Sr uptake potential of a system. For example, dissolved organic carbon (at levels typical of groundwaters) can suppress crystal growth. As a result, the continuous nucleation of small crystals, rather than growth of existing crystals, may be the dominant mode of precipitation. This has the potential for greater uptake of Sr because the smaller crystal sizes associated with nucleated calcite may more readily accommodate the distortion resulting from substitution of the larger Sr ion for Ca ions than can larger crystals. However, these smaller crystals may also be less stable and over the long term release Sr as a result of Ostwald ripening. To better understand the formation and composition of relevant calcium carbonate mineral phases two related series of mineral precipitation experiments were conducted. The first series of experiments, conducted using a Continuously Stirred Tank Reactor (CSTR) operated at steady state rates of precipitation was focused on understanding the

  1. NON-ISOTHERMAL CRYSTALLIZATION OF ETHYLENE-VINYL ACETATE COPOLYMER CONTAINING A HIGH WEIGHT FRACTION OF GRAPHENE NANOSHEETS AND CARBON NANOTUBES

    Institute of Scientific and Technical Information of China (English)

    Huan Pang; Gan-ji Zhong; Jia-zhuang Xu; Ding-xiang Yan; Xu Ji; Zhong-ming Li; Chen Chen

    2012-01-01

    The effect of the different geometrical dimensionality of two dimensional graphene nanosheets (2D GNSs) and one dimensional carbon nanotubes (1D CNTs) on the non-isothermal crystallization of an ethylene-vinyl acetate (EVA) copolymer at high loading (5 wt%) was studied.Transmission electron microscopy indicated a homogeneous dispersion of GNSs and CNTs in EVA obtained by a solution dispersion process.Fourier-transform infrared spectroscopy and differential scanning calorimetry measurements showed that 1D CNTs and 2D GNSs acted as effective nucleating agents,with a noticeably increased onset crystallization temperature of EVA.A high weight fraction of nano-fillers slowed the overall crystallization rate of composites.At the same crystallization temperature,the crystallization behavior of GNS/EVA composites was slowed compared to that of the CNT/EVA ones owing to larger nucleus barrier and activation energy of diffusion.Dynamic mechanical relaxation and rheology behavior of CNT/EVA and GNS/EVA composites demonstrated that the planar structure of the GNSs had an intensively negative effect on EVA chain mobility due to interactions between nanofillers and polymer chains,as well as spatial restriction.

  2. 二氧化碳驱油藏沥青质沉淀量测量装置的实验研究%Experimental Study on Measuring Asphaltene Precipitation Volume in Carbon Dioxide Flooding Reservoir

    Institute of Scientific and Technical Information of China (English)

    胡杰; 何岩峰; 李栋; 王红梅; 李华明; 李森林

    2011-01-01

    设计了一套二氧化碳驱油藏沥青质沉淀量测量装置,该装置采用全密闭流程,借助计算机实现控制并做数据采集,对产出的气体进行同步气相色谱分析.使用该装置对某油田的二氧化碳驱进行实验分析,最终得出了地层温度、驱替压力对二氧化碳驱沥青质沉淀的影响关系.%A device boasting of a fully-enclosed process, and computer control and data acquisition was designed to measure asphaltene precipitation volume in carbon dioxide flooding reservoir and analyze the gas with gas chromatography. The designed device can withstand high pressures and temperatures and acid. The experimental analysis shows that this device helps obtain effects of both ground temperature and displacement pressure on the asphaltene precipitation in carbon dioxide flooding reservoir.

  3. An analysis of the shape of a luminescence band induced by free electron-to-carbon atom transitions in semi-insulating undoped GaAs crystals

    CERN Document Server

    Glinchuk, K D; Prokhorovich, A V; Strilchuk, O N

    2001-01-01

    The shape of a photoluminescence (band observed due to recombination of free electrons on carbon atoms) in semi-insulating undoped GaAs crystals is analyzed at different temperatures (T=4.8 to 77 K). It is shown that at low temperatures the shape essentially differs from the theoretical one while at high temperatures is very close to it for radiative transitions of free electrons to isolated shallow acceptors. The observed difference of the experimental and theoretical shapes of the photoluminescence band is connected with the broadening of carbon-induced acceptor levels, resulting from the influence of electric fields of randomly distributed ionized acceptors and donors on isolated carbon atoms. Coincidence of the shapes is connected with a considerable in the energy of free carriers

  4. Role of crystal structure on CO2 capture by limestone derived CaO subjected to carbonation/recarbonation/calcination cycles at Ca-looping conditions

    International Nuclear Information System (INIS)

    Highlights: • CO2 capture of limestone subjected to carbonation/recarbonation/calcination cycles is affected by diffusion. • A reduction of crystallinity by ball milling favors diffusion and promotes recarbonation. • Thermal annealing enhances crystallinity and hinders recarbonation. • Milling promotes friability whereas annealing enhances the resistance of particles to fragmentation. • The solid crystal structure determines the efficiency of the novel Ca-looping concept. - Abstract: Large scale pilot plants are currently demonstrating the feasibility of the Calcium-looping (CaL) technology built on the multicyclic calcination/carbonation of natural limestone for post-combustion and pre-combustion CO2 capture. Yet, limestone derived CaO exhibits a drop of conversion when subjected to multiple carbonation/calcination cycles, which lessens the efficiency of the technology. In this paper we analyze a novel CaL concept recently proposed to mitigate this drawback based on the introduction of an intermediate stage wherein carbonation is intensified at high temperature and high CO2 partial pressure. It is shown that carbonation in this stage is mainly driven by solid-state diffusion, which is determined by the solid’s crystal structure. Accordingly, a reduction of crystallinity by ball milling, which favors diffusion, serves to promote recarbonation. Conversely, thermal annealing, which enhances crystallinity, hinders recarbonation. An initial fast phase has been identified in the recarbonation stage along which the rate of carbonation is also a function of the crystal structure indicating a relevant role of surface diffusion. This is consistent with a recently proposed mechanism for nucleation of CaCO3 on the CaO surface in islands with a critical size determined by surface diffusion. A further issue analyzed has been the effects of pretreatment and cycling on the mechanical strength of the material, whose fragility hampers the CaL process efficiency

  5. Immature crude oils in the salt lake depositionalenvironment are related to organic matter precipitated atstage of carbonate in salt lake sedimentation sequences

    Institute of Scientific and Technical Information of China (English)

    2000-01-01

    The present paper studies the mineralogy and geochemistry of a geological section in Jianghan basin. Widely distributed immature oils in this basin have been shown to relate to the carbonate depositional stage of salt lake sedimentation cycle. It is concluded that only when the content of organic carbon in the rocks is taken into account, is it meaningful to calculate the immature oil in the source rocks.

  6. 低碳钛、钒微合金钢中的相间析出%Interphase precipitation in low carbon Ti-V microalloyed steels

    Institute of Scientific and Technical Information of China (English)

    贾涛; 魏娇; 冯洁; 张维娜; 刘振宇; 王国栋

    2014-01-01

    The present study focuses on the Ti-V microalloying system which draws less attention. By using the Formaster-FII dilatometer,the sample was held at austenite/ferrite dual-phase temperature region and the Ti-V complex interphase precipitates were obtained during the austenite to ferrite transformation. Optical Microscopy (OM) and transmission electron microscopy (TEM) were employed to analyze the microstructure , especially the morphology of the interphase precipitate and its crystallographic orientation relationship with ferrite matrix. Studies show that 650℃is the nose temperature for static isothermal transforma-tion. The interphase precipitates exhibit sheet-like distribution,including flat and curved sheets and adopt Baker-Nutting orientation relationships with the ferrite matrix.%针对目前较少关注的Ti-V微合金体系,在Formaster-FII膨胀仪上进行奥氏体/铁素体两相区等温,在铁素体相变同时获得Ti、V复合相间析出。采用金相、透射电子显微镜对显微组织、尤其是相间析出形貌、及其与铁素体基体的位向关系进行了观察与分析。研究表明,650℃为静态等温相变的鼻温点,相间析出呈层状分布,具有平面和曲面两种形貌,相间析出碳化物与铁素体基体之间存在Baker-Nutting取向关系。

  7. Self-formation of highly aligned metallic, semiconducting and single chiral single-walled carbon nanotubes assemblies via a crystal template method

    Energy Technology Data Exchange (ETDEWEB)

    Kawai, Hideki; Hasegawa, Kai; Yanagi, Kazuhiro, E-mail: yanagi-kazuhiro@tmu.ac.jp [Department of Physics, Tokyo Metropolitan University, Hachioji, Tokyo 192-0397 (Japan); Oyane, Ayako [Nanosystem Research Institute, National Institute of Advanced Industrial Science and Technology (AIST), Tsukuba, Ibaraki 305-8562 (Japan); Naitoh, Yasuhisa [Nanosystem Research Institute, National Institute of Advanced Industrial Science and Technology (AIST), Tsukuba, Ibaraki 305-8564 (Japan)

    2014-09-01

    The fabrication of an aligned array of single-walled carbon nanotubes (SWCNTs) with a single chiral state has been a significant challenge for SWCNT applications as well as for basic science research. Here, we developed a simple, unique technique to produce assemblies in which metallic, semiconducting, and single chiral state SWCNTs were densely and highly aligned. We utilized a crystal of surfactant as a template on which mono-dispersed SWCNTs in solution self-assembled. Micro-Raman measurements and scanning electron microscopy measurements clearly showed that the SWCNTs were highly and densely aligned parallel to the crystal axis, indicating that approximately 70% of the SWCNTs were within 7° of being parallel. Moreover, the assemblies exhibited good field effect transistor characteristics with an on/off ratio of 1.3 × 10{sup 5}.

  8. Influence of Substrate Mineralogy on Bacterial Mineralization of Calcium Carbonate: Implications for Stone Conservation

    OpenAIRE

    Rodriguez-Navarro, Carlos; Jroundi, Fadwa; Schiro, Mara; Ruiz-Agudo, Encarnación; González-Muñoz, María Teresa

    2012-01-01

    The influence of mineral substrate composition and structure on bacterial calcium carbonate productivity and polymorph selection was studied. Bacterial calcium carbonate precipitation occurred on calcitic (Iceland spar single crystals, marble, and porous limestone) and silicate (glass coverslips, porous sintered glass, and quartz sandstone) substrates following culturing in liquid medium (M-3P) inoculated with different types of bacteria (Myxococcus xanthus, Brevundimonas diminuta, and a carb...

  9. Graphene and carbon black nano-composite polymer absorbers for a pyro-electric solar energy harvesting device based on LiNbO3 crystals

    International Nuclear Information System (INIS)

    Highlights: • A novel scheme for solar energy harvesting based on pyroelectric effect is proposed. • An optical system focusing solar radiation onto a LiNbO3 crystal is used. • Graphene and carbon black nano-composite polymer absorbers used as coating. • This configuration increases the amplitude of temperature variation experienced. • The whole solar spectrum is involved in the energy harvesting mechanism. - Abstract: A novel scheme for solar energy harvesting based on the pyro-electric effect has been demonstrated. The proposed harvester is based on an optical system focusing solar radiation onto a ferroelectric crystal (i.e. lithium niobate). The face exposed to the heating source is coated with a nanocomposite material (i.e. carbon black and graphene particles) that greatly improves the adsorption of solar radiation. The solar energy focused onto the crystal through a simple optical system allows one to induce a thermal gradient able to generate electric charges. Experiments have been carried out indoor as well as outdoor (in Pozzuoli, Naples, Italy, on December). Results show that two configurations appear to be preferable: (a) pyro-electric element with carbon black-based coating and a Fresnel lens (surface of about 100 cm2); (b) pyro-electric element with graphene-based coating and a Fresnel lens (surface of about 600 cm2). In both experimental arrangements the maximum temperature variation reached locally onto the lithium niobate substrate is relatively high with peaks greater than 250 °C. The maximum electrical power peak is of about 90 μW and about 50 μW for (a) and (b) respectively. The results of this first investigation are encouraging for further development of more efficient harvesting devices

  10. Dependence on injection temperature and on aquifer's petrophysical properties of the local stress applying on the pore wall of a crystallized pore in the context of CO2 storage in deep saline aquifers

    Science.gov (United States)

    Osselin, Florian; Fen-Chong, Teddy; Fabbri, Antonin; Lassin, Arnault; Pereira, Jean-Michel; Dangla, Patrick

    2013-11-01

    The development of CCS (carbon capture and storage) currently faces numerous problems and particularly the precipitation of salts induced by the drying of the porous medium during injection of carbon dioxide in deep saline aquifers. This precipitation has several consequences, and particularly the creation of a crystallization pressure which can have an important mechanical impact on the host rock. Literature on crystallization pressure is one century rich of experimental and theoretical works. However, applications have been performed in the field of civil engineering and building science only, and, despite they are of paramount importance in the context of CCS, studies about this phenomenon in deep reservoir conditions are currently lacking. In this paper, we retrieve the classic crystallization pressure equation within the framework of geochemistry and present its explicit form of dependence with temperature, pressure, and composition. Evaluation of the crystallization pressure has then been proceeded considering the injection conditions and a sketch of in-pore crystallization process. The evolution of the local stress transmitted to a crystallized pore wall is found to be strongly related to the petrophysical properties of the medium and to the injection temperature of the carbon dioxide under the assumption of constant salt concentration during the precipitation process. Values differ strongly with the considered mineral, depending particularly on the solubility, and can reach in some conditions 165 MPa, making crystallization pressure a major factor in the mechanical behavior of the aquifer.

  11. Struvite Precipitation and Biological Dissolutions.

    OpenAIRE

    Ezquerro, Ander

    2010-01-01

    Struvite is a salt that is formed out of  Mg2+,NH4+ and PO43- and it crystallizes in form of MgNH4PO4.6H2O. Struvite‟s (magnesium ammonium phosphate or MAP) precipitation has recently been regarded as an interesting technique to remove phosphate and ammonium from waste water. The high elimination rates and the possibility of recycling the struvite as a direct slow release fertilizer make this process feasible and appealing. However, the costs due to the raw chemicals needed are drawbacks that...

  12. Constraints on the factors controlling 13C-18O bond abundances in biologically precipitated carbonates from measurements of marine calcifiers cultured at variable temperature, pH, and salinity

    Science.gov (United States)

    Conchas, T. E.; Eagle, R.; Eiler, J. M.; Ries, J. B.; Freitas, P. S.; Hiebenthal, C.; Wanamaker, A. D.; Tripati, A. K.

    2012-12-01

    Marine mollusks and corals are widely used as archives of past climate change; oxygen isotopic composition (δ18O value) of their carbonate minerals is perhaps the most commonly used proxy to reconstruct paleoclimate from these marine calcifiers. However, oxygen isotope paleothermometry of mollusks and corals is complicated by non-equilibrium "vital effects" and variations in seawater pH changes, both of which influence the net fractionation of oxygen isotopes between carbonate and water. Carbonate "clumped isotope" thermometry is an emerging approach that potentially addresses these ambiguities. Here we report measurements of abundance of 13C-18O bonds (described by the measured parameter Δ47) in a variety of marine calcifiers cultured under controlled conditions. Previous studies on biologically precipitated samples such as foraminifera, coccoliths, and corals have shown that Δ47 values are related to calcification temperature with a relationship that is generally similar to inorganic carbonate. However, the influence of effects other than temperature has not been extensively studied and little work has been done to explore the potential for small non-equilibrium effects in cultured specimens that were grown under controlled conditions. In this study, we report δ18O and Δ47 measurements of mollusk specimens that were cultured at several temperatures ranging from 5 to 25°C, as well as different pH and salinity values. We also report data for other marine calcifiers including the temperate coral species Oculina arbuscula and the coralline red algae Neogoniolithon sp., that were cultured at a single temperature but variable pH.

  13. 铁碳微电解+混凝法预处理高盐染料废水的研究%Treatment of High-salt Dye Wastewater by Iron-carbon Microelectrolysis+Coagulative Precipitation Process

    Institute of Scientific and Technical Information of China (English)

    马正慧; 何义亮; 冯丽梅; 杨军

    2011-01-01

    对高盐染料废水先采用铁碳微电解法进行处理,出水再经过加石灰混凝进行处理.确定了最佳处理条件:微电解反应时间为5h,pH为3,铁碳质量比为1:2,微电解出水加石灰调节pH值至9左右后混凝沉淀3h.试验结果表明:系统对COD、色度的去除率分别为40.09%和60.1%,废水的可生化性提高到0.32,达到了预处理的效果.%The iron-carbon micro-electrolysis-lime coagulation combined process is used to treat the high-salt dye wastewater. The influence of reaction time, pH, and the volume ratio of iron to carbon is studied. The best treastment conditions are determined. The results show that when the electrolysis reaction time is 5 h, the pH is 3, the volume ratio of iron to carbon in the iron-carbon micro-electrolysis unit is 1: 2, the effluent pH of the micro-electrolysis unit is alkalized to about 9 by lime, and coagulative precipitation is 3 h,then the wastewater COD and color removal rate can reach 40. 09% and 60. 1 %, respectively. The biodegrad-ability of wastewater increases to 0. 32,reaching the pretreatment effect.

  14. Specific Surface versus Electrochemically Active Area of the Carbon/Polypyrrole Capacitor: Correlation of Ion Dynamics Studied by an Electrochemical Quartz Crystal Microbalance with BET Surface.

    Science.gov (United States)

    Mosch, Heike L K S; Akintola, Oluseun; Plass, Winfried; Höppener, Stephanie; Schubert, Ulrich S; Ignaszak, Anna

    2016-05-10

    Carbon/polypyrrole (PPy) composites are promising electrode materials for energy storage applications such as lightweight capacitors. Although these materials are composed of relatively inexpensive components, there is a gap of knowledge regarding the correlation between surface, porosity, ion exchange dynamics, and the interplay of the double layer capacitance and pseudocapacitance. In this work we evaluate the specific surface area analyzed by the BET method and the area accessible for ions using electrochemical quartz-crystal microbalance (EQCM) for SWCNT/PPy and carbon black Vulcan XC72-R/PPy composites. The study revealed that the polymer has significant influence on the pore size of the composites. Although the BET surface is low for the polypyrrole, the electrode mass change and thus the electrochemical area are large for the polymer-containing electrodes. This indicates that multiple redox active centers in the charged polymer chain are good ion scavengers. Also, for the composite electrodes, the effective charge storage occurs at the polypyrrole-carbon junctions, which are easy to design/multiply by a proper carbon-to-polymer weight ratio. The specific BET surface and electrochemically accessible surface area are both important parameters in calculation of the electrode capacitance. SWCNTs/PPy showed the highest capacitances normalized to the BET and electrochemical surface as compared to the polymer-carbon black. TEM imaging revealed very homogeneous distribution of the nanosized polymer particles onto the CNTs, which facilitates the synergistic effect of the double layer capacitance (CNTs) and pseudocapacitance (polymer). The trend in the electrode mass change in correlation with the capacitance suggest additional effects such as a solvent co-insertion into the polymer and the contribution of the charge associated with the redox activity of oxygen-containing functional groups on the carbon surface. PMID:27082127

  15. On the electric double-layer structure at carbon electrode/organic electrolyte solution interface analyzed by ac impedance and electrochemical quartz-crystal microbalance responses

    Energy Technology Data Exchange (ETDEWEB)

    Kim, In-Tae; Egashira, Minato; Yoshimoto, Nobuko [Department of Applied Chemistry, Graduate School of Science and Engineering, Yamaguchi University, 2-16-1, Tokiwadai, Ube 755-8611 (Japan); Morita, Masayuki, E-mail: morita@yamaguchi-u.ac.jp [Department of Applied Chemistry, Graduate School of Science and Engineering, Yamaguchi University, 2-16-1, Tokiwadai, Ube 755-8611 (Japan)

    2011-08-30

    Highlights: {center_dot} We monitored resonance frequency change of smooth surface carbon electrode to determine mass changes during electrochemical polarization.{center_dot} This was done from viewpoints of ensuring the electric double-layer structure in organic electrolytes.{center_dot} Clear difference was observed in the mass changes among the electrolyte composition.{center_dot} It were related with differences in the double-layer capacitance at carbon. - Abstract: ac impedance and electrochemical quartz crystal microbalance (EQCM) techniques have been applied to analyze the structure of electric double-layer formed at carbon/organic electrolyte solution interface using a sputtered carbon electrode. The mass changes caused by electrochemical adsorption (accumulation) of ions have been estimated in the solutions of propylene carbonate (PC) dissolving tetrafluoroborate (BF{sub 4}{sup -}) salts of lithium (Li{sup +}), tetraethylammonium (TEA{sup +}) and tetra-n-butylammonium (TBA{sup +}) cations. The observed mass changes during the cathodic polarization in the solutions containing TEA{sup +} and TBA{sup +} were well consistent with those expected by the calculation based on mono-layer adsorption of the cations with giving the consideration to the surface roughness. On the other hand, the mass change observed in the solution containing Li{sup +} salt showed that the solvation of Li{sup +} with three or four molecules of PC would be the charge compensation species at the interface. Comparison of the quantity of the electricity passed during the EQCM measurements with that from theoretical calculation with simple Helmholtz-layer model revealed that the major part of the double-layer capacitance would be based on the electrostatic polarization of the solvent molecule directly adsorbed at the carbon surface.

  16. Modelled Precipitation Over Greenland

    Data.gov (United States)

    National Aeronautics and Space Administration — This data set includes the annual total precipitation from 1985 to 1999 and monthly total precipitation from January 1985 to December 1999. The data is derived from...

  17. Interpretation of the vacancy-ordering controlled growth morphology of Hg{sub 5}In{sub 2}Te{sub 8} precipitates in Hg{sub 3}In{sub 2}Te{sub 6} single crystals by TEM observation and crystallographic calculation

    Energy Technology Data Exchange (ETDEWEB)

    Sun, Jie [State Key Laboratory of Solidification Processing, Northwestern Polytechnical University, 127 Youyi Road, Xi’an (China); School of Chemical and Biomolecular Engineering, The University of Sydney, NSW 2006 (Australia); Australian Centre for Microscopy and Microanalysis, The University of Sydney, NSW 2006 (Australia); Fu, Li, E-mail: fuli@nwpu.edu.cn [State Key Laboratory of Solidification Processing, Northwestern Polytechnical University, 127 Youyi Road, Xi’an (China); Liu, Hongwei [Australian Centre for Microscopy and Microanalysis, The University of Sydney, NSW 2006 (Australia); Ringer, S.P. [Australian Centre for Microscopy and Microanalysis, The University of Sydney, NSW 2006 (Australia); School of Aerospace, Mechanical and Mechatronic Engineering, The University of Sydney, NSW 2006 (Australia); Liu, Zongwen, E-mail: zongwen.liu@sydney.edu.au [School of Chemical and Biomolecular Engineering, The University of Sydney, NSW 2006 (Australia)

    2015-02-15

    Graphical abstract: The growth morphology and detailed crystallography of Hg{sub 5}In{sub 2}Te{sub 8} precipitates in Hg{sub 3}In{sub 2}Te{sub 6} matrix to has been interpreted by means of transmission electron microscopy and invariant element deformation model. Three crystallographic equivalent variants of Hg{sub 5}In{sub 2}Te{sub 8} precipitates in Hg{sub 3}In{sub 2}Te{sub 6} matrix were found to have different growth directions and habit planes. Such growth morphology is fully attributed to the lattice shrinkage induced by vacancy ordering under high temperature in Hg{sub 5}In{sub 2}Te{sub 8}. Through near coincident site lattice and invariant strain calculation, the morphology and crystallographic features of the precipitate has been successfully interpreted. - Highlights: • The growth morphology of Hg{sub 5}In{sub 2}Te{sub 8} precipitates in Hg{sub 3}In{sub 2}Te{sub 6} was observed by TEM. • Near-CSL calculation show 0.7577% lattice shrinkage of Hg{sub 5}In{sub 2}Te{sub 8} at high temperature. • All the involved factors have inverse relationship with the move speed of interface. • The calculated crystallography features of Hg{sub 5}In{sub 2}Te{sub 8} agree well with the TEM results. - Abstract: Generally, the crystal growth morphology in liquid or vapor was controlled by chemical potential, while that in solid solute was restricted by 3D strain matching between matrix and secondary phase. It is already known that the growth and evolution of the morphology of secondary phase during the solid phase transformation are highly determined by the variation of interface energy induced by lattice mismatch. In this work, the growth morphology and crystallography of Hg{sub 5}In{sub 2}Te{sub 8} precipitates in Hg{sub 3}In{sub 2}Te{sub 6} matrix were investigated by means of transmission electron microscopy (TEM). It was found that the growth of Hg{sub 5}In{sub 2}Te{sub 8} precipitates displayed an unusual growth morphology which contain three crystallographically

  18. PHOSPHATE MANAGEMENT: FY2010 RESULTS OF PHOSPHATE PRECIPITATION TESTS

    Energy Technology Data Exchange (ETDEWEB)

    Hay, M.; King, W.

    2011-04-04

    The Phosphate Management program seeks to develop treatment options for caustic phosphate solutions resulting from the caustic leaching of the bismuth phosphate sludge. The SRNL subtask investigated the precipitation of phosphate salts from caustic solutions through addition of fluoride and by crystallization. The scoping tests examined the: precipitation of phosphate by the addition of sodium fluoride to form the sodium fluorophosphate double salt, Na{sub 7}F(PO{sub 4}){sub 2} {center_dot} 19H{sub 2}O, crystallization of phosphate by reducing the temperature of saturated phosphate solutions, and combinations of precipitation and crystallization. A simplified leachate simulant was used in the study produced by dissolving sodium phosphate in 1 M to 3.5 M sodium hydroxide solutions. The results show that all three processes; precipitation with sodium fluoride, crystallization, and combined precipitation/crystallization can be effective for removing large amounts of phosphate from solution. The combined process of precipitation/crystallization showed >90% removal of phosphate at all hydroxide concentrations when cooling a non-saturated phosphate solution from 65 C to 25 C. Based on the measured solubility of sodium phosphate, pH adjustment/caustic addition will also remove large amounts of phosphate from solution (>80%). For all three processes, the phosphate concentration in the caustic solution must be managed to keep the phosphate from becoming too concentrated and thereby potentially forming a solid mass of sodium phosphate after an effective phosphate removal process.

  19. Melting, growth, and faceting of lead precipitates in aluminum

    DEFF Research Database (Denmark)

    Gråbæk, L.; Bohr, J.; Andersen, H.H.;

    1992-01-01

    Aluminum single crystals cut in the direction were implanted with 2 x 10(20) m-2 Pb+ ions at 75 or 150 keV. The implanted insoluble lead precipitated as epitaxially oriented crystallites in the aluminum matrix. The precipitates were studied by x-ray diffraction at Riso, DESY, and Brookhaven...

  20. Investigating the early stages of mineral precipitation by potentiometric titration and analytical ultracentrifugation.

    Science.gov (United States)

    Kellermeier, Matthias; Cölfen, Helmut; Gebauer, Denis

    2013-01-01

    Despite the importance of crystallization for various areas of research, our understanding of the early stages of the mineral precipitation from solution and of the actual mechanism of nucleation is still rather limited. Indeed, detailed insights into the processes underlying nucleation may enable a systematic development of novel strategies for controlling mineralization, which is highly relevant for fields ranging from materials chemistry to medicine. In this work, we describe experimental aspects of a quantitative assay, which relies on pH titrations combined with in situ metal ion potentiometry and conductivity measurements. The assay has originally been designed to study the crystallization of calcium carbonate, one of the most abundant biominerals. However, the developed procedures can also be readily applied to any compound containing cations for which ion-selective electrodes are available. Besides the possibility to quantitatively assess ion association prior to nucleation and to directly determine thermodynamic solubility products of precipitated phases, the main advantage of the crystallization assay is the unambiguous identification of the different stages of precipitation (i.e., prenucleation, nucleation, and early postnucleation) and the characterization of the multiple effects of additives. Furthermore, the experiments permit targeted access to distinct precursor species and intermediate stages, which thus can be analyzed by additional methods such as cryo-electron microscopy or analytical ultracentrifugation (AUC). Regarding ion association in solution, AUC detects entities significantly larger than simple ion pairs, so-called prenucleation clusters. Sedimentation coefficient values and distributions obtained for the calcium carbonate system are discussed in light of recent insights into the structural nature of prenucleation clusters.

  1. In situ absorption of molybdate and vanadate during precipitation of hydrotalcite from sodium aluminate solutions

    Science.gov (United States)

    Smith, Howard D.; Parkinson, Gordon M.; Hart, Robert D.

    2005-02-01

    Reaction with seawater to produce the layered double hydroxide hydrotalcite is an important means for amelioration of Bayer process wastewater prior to its disposal into the marine environment. This reaction has been synthesised under controlled conditions to elucidate the principal mechanisms involved, particularly those related to absorption of transition metals that are removed from solution. Magnesium-aluminium layered double hydroxides precipitated from reaction between magnesium chloride and synthetic sodium aluminate solution in the presence of transition metal oxyanions have been prepared and characterised using thermal, X-ray and microscopic techniques. The layered double hydroxide precipitated at pH >13 is found to consist of nano-sized hexagonal crystals of final magnesium-aluminium ratio of 2:1, while that precipitated at pHprecipitation is a pH dependent process. Transition metals are found to replace carbonate in the interlayer space but have little or no overall effect on crystal size or structure. Interlayer distance remains constant in the presence of transition metals, suggesting that these species are intercalated as simple monomeric or dimeric oxyanions, rather than larger polymeric forms.

  2. Growth of Organic Crystals by Ostwald Ripening

    Science.gov (United States)

    Egbert, W.; Podsiadly, C.; Naumann, R.

    1985-01-01

    The objective of this investigation is to evaluate the growth of various organic crystals by chemical precipitation and Ostwald ripening. Six precipitation reactors were flown on STS-51A. Five of the reactors contained proprietary materials. The sixth contained urea dissolved in ethanol with toluene as the precipitating agent. The size distribution will be analyzed and compared with a similar model being developed.

  3. Gas-Liquid Precipitation of Water Dissolved Heavy Metal Ions Using Hydrogen Sulfide Gas

    NARCIS (Netherlands)

    Al-Tarazi, Mousa

    2004-01-01

    Precipitation of solids promoted by gas-liquid reactions is applied in many industrial processes such as the production of ammonium phosphate, ammonium sulphate, barium carbonate, calcium carbonate, calcium fluoride, ypsum (calcium sulphate), goethite, sodium bicarbonate, strontium carbonate and te

  4. Bench-Scale Development of a Hot Carbonate Absorption Process with Crystallization-Enabled High-Pressure Stripping for Post-Combustion CO{sub 2} Capture

    Energy Technology Data Exchange (ETDEWEB)

    Lu, Yongqi; DeVries, Nicholas; Ruhter, David; Manoranjan, Sahu; Ye, Qing; Ye, Xinhuai; Zhang, Shihan; Chen, Scott; Li, Zhiwei; O' Brien, Kevin

    2014-03-31

    A novel Hot Carbonate Absorption Process with Crystallization-Enabled High-Pressure Stripping (Hot-CAP) has been developed by the University of Illinois at Urbana-Champaign and Carbon Capture Scientific, LLC in this three-year, bench-scale project. The Hot-CAP features a concentrated carbonate solution (e.g., K{sub 2}CO{sub 3}) for CO{sub 2} absorption and a bicarbonate slurry (e.g., KHCO{sub 3}) for high-pressure CO{sub 2} stripping to overcome the energy use and other disadvantages associated with the benchmark monoethanolamine (MEA) process. The project was aimed at performing laboratory- and bench-scale experiments to prove its technical feasibility and generate process engineering and scale-up data, and conducting a techno-economic analysis (TEA) to demonstrate its energy use and cost competitiveness over MEA. To meet project goals and objectives, a combination of experimental, modeling, process simulation, and economic analysis studies were applied. Carefully designed and intensive experiments were conducted to measure thermodynamic and reaction engineering data relevant to four major unit operations in the Hot-CAP (i.e., CO{sub 2} absorption, CO{sub 2} stripping, bicarbonate crystallization, and sulfate reclamation). The rate promoters that could accelerate the CO{sub 2} absorption rate into the potassium carbonate/bicarbonate (PCB) solution to a level greater than that into the 5 M MEA solution were identified, and the superior performance of CO{sub 2} absorption into PCB was demonstrated in a bench-scale packed-bed column. Kinetic data on bicarbonate crystallization were developed and applied for crystallizer design and sizing. Parametric testing of high-pressure CO{sub 2} stripping with concentrated bicarbonate-dominant slurries at high temperatures ({>=}140{degrees}C) in a bench-scale stripping column demonstrated lower heat use than with MEA. The feasibility of a modified process for combining SO{sub 2} removal with CO{sub 2} capture was preliminarily

  5. Grafting of a functionalized side-chain liquid crystal polymer on carbon fiber surfaces: Novel coupling agents for fiber/polymer matrix composites

    Energy Technology Data Exchange (ETDEWEB)

    Le Bonheur, V.; Stupp, S.I. (Univ. of Illinois, Urbana, IL (United States))

    1993-09-01

    The authors studied covalent grafting to functionalized carbon fibers of a specially designed liquid crystalline monomer and its corresponding side-chain liquid crystalline polymer containing pendant chemical functions on their mesogenic groups. From a materials point of view these liquid crystalline compounds could act as coupling agents at fiber/polymer matrix interfaces, offering a mechanism to control composite properties not only through bonding but also through their [open quotes]spontaneous[close quotes] molecular orientation in interfacial regions. The grafting methodology for both monomer and polymer to fiber surfaces involved esterification through carbodiimide chemistry in solution. Carboxylic acid groups found on functionalized carbon fiber surfaces were esterified to phenolic functions in the side chains of the experimental polymer. Following grafting procedures the fibers were analyzed by scanning electron microscopy (SEM) and by contact angle measurements. SEM micrographs of fibers grafted with polymer revealed the presence of strongly attached polymeric material on the graphitic surface after rigorous extraction with polymer solvent. Contact angle measurements and polar/dispersive free energy analysis indicated also a smaller polar component of the surface free energy of fibers possibly due to the hydrophobic polymer backbone grafted on the carbon surfaces. On the basis of results, it is concluded that the esterification reaction grafted the polyphenolic liquid-crystal polymer on graphite fiber surfaces. 24 refs., 8 figs., 4 tabs.

  6. Crystallization from Gels

    Science.gov (United States)

    Narayana Kalkura, S.; Natarajan, Subramanian

    Among the various crystallization techniques, crystallization in gels has found wide applications in the fields of biomineralization and macromolecular crystallization in addition to crystallizing materials having nonlinear optical, ferroelectric, ferromagnetic, and other properties. Furthermore, by using this method it is possible to grow single crystals with very high perfection that are difficult to grow by other techniques. The gel method of crystallization provides an ideal technique to study crystal deposition diseases, which could lead to better understanding of their etiology. This chapter focuses on crystallization in gels of compounds that are responsible for crystal deposition diseases. The introduction is followed by a description of the various gels used, the mechanism of gelling, and the fascinating phenomenon of Liesegang ring formation, along with various gel growth techniques. The importance and scope of study on crystal deposition diseases and the need for crystal growth experiments using gel media are stressed. The various crystal deposition diseases, viz. (1) urolithiasis, (2) gout or arthritis, (3) cholelithiasis and atherosclerosis, and (4) pancreatitis and details regarding the constituents of the crystal deposits responsible for the pathological mineralization are discussed. Brief accounts of the theories of the formation of urinary stones and gallstones and the role of trace elements in urinary stone formation are also given. The crystallization in gels of (1) the urinary stone constituents, viz. calcium oxalate, calcium phosphates, uric acid, cystine, etc., (2) the constituents of the gallstones, viz. cholesterol, calcium carbonate, etc., (3) the major constituent of the pancreatic calculi, viz., calcium carbonate, and (4) cholic acid, a steroidal hormone are presented. The effect of various organic and inorganic ions, trace elements, and extracts from cereals, herbs, and fruits on the crystallization of major urinary stone and gallstone

  7. Diffusion-driven precipitate growth and ripening of oxygen precipitates in boron doped silicon by dynamical x-ray diffraction

    OpenAIRE

    Will, Johannes; Gröschel, A.; Bergmann, C.; Spiecker, E.; Magerl, A.

    2014-01-01

    X-ray Pendellösung fringes from three silicon single crystals measured at 900 °C are analyzed with respect to density and size of oxygen precipitates within a diffusion-driven growth model and compared with TEM investigations. It appears that boron doped (p+) material shows a higher precipitate density and a higher strain than moderately (p-) boron crystals. In-situ diffraction reveals a diffusion-driven precipitate growth followed by a second growth regime in both materials. An interpretatio...

  8. Thermodynamic Calculation of Carbide Precipitate in Niobium Microalloyed Steels

    Institute of Scientific and Technical Information of China (English)

    XU Yun-bo; YU Yong-mei; LIU Xiang-hua; WANG Guo-dong

    2006-01-01

    On the basis of regular solution sublattice model, thermodynamic equilibrium of austenite/carbide in Fe-Nb-C ternary system was investigated. The equilibrium volume fraction, chemical driving force of carbide precipitates and molar fraction of niobium and carbon in solution at different temperatures were evaluated respectively. The volume fraction of precipitates increases, molar fraction of niobium dissolved in austenite decreases and molar fraction of carbon increases with decreasing the niobium content. The driving force increases with the decrease of temperature, and then comes to be stable at relatively low temperatures. The predicted ratio of carbon in precipitates is in good agreement with the measured one.

  9. Microbially Induced Precipitation of Strontianite Nanoparticles.

    Science.gov (United States)

    Kang, Serku; Yumi Kim; Lee, Young Jae; Roh, Yul

    2015-07-01

    The objectives of this study were to investigate the microbially mediated precipitation of strontium by microorganisms, and to examine the mineralogical characteristics of the precipitates. Wu Do-1 (Proteus mirabilis) enriched from rhodoliths was used to precipitate strontium at room temperature under aerobic environment. The growth of Wu Do-1 gradually increased over 16 days (OD600 = 2.6) and then decreased until 22 days (OD600 = 2.0) during microbial incubation for strontium precipitation. Also, the pH decreased from 6.5 to 5.3 over 4 days of incubation due to microbial oxidation of organic acids, and then the pH increased up to 8.6 at 25 days of incubation due to NH3+ generation. The Sr2+ concentration in the biotic group sharply decreased from 2,953 mg/L to 5.7 mg/L over 29 days of incubation. XRD, SEM-/TEM-EDS analyses revealed that the precipitates formed by Wu Do-1 (Proteus mirabilis) were identified as 20-70 nm sized strontianite (SrCO3). Therefore, these results suggested that formation of sparingly soluble Sr precipitates mediated by Wu Do-1 (Proteus mirabilis) sequesters strontium and carbon dioxide into a more stable and less toxic form such as strontianite (SrCO3). These results also suggest that bioremediation of metal-contaminated water and biominealization of carbonate minerals may be feasible in the marine environment.

  10. Effect of precipitation procedure and detection technique on particle size distribution of CaCO 3

    Science.gov (United States)

    Martos, C.; Coto, B.; Peña, J. L.; Rodríguez, R.; Merino-Garcia, D.; Pastor, G.

    2010-09-01

    The deposition of inorganic salts ("scales") such as calcium carbonate is an important flow assurance problem during crude oil production. The knowledge of the features of the precipitated solids, mainly the particle size and morphology, is crucial to understand the nature of the solids and to avoid or reduce the effect of their deposition. For instance, the use of additives is one of the most usual procedures to mitigate this problem. Additives interact with scale-forming substances either by increasing the induction time, or by inhibiting crystal growth, changing the morphology of solids. In this work, CaCO 3 was precipitated by two different experimental methods: by mixing sodium carbonate and calcium chloride at 25 °C (method 1), and by changing the pH (method 2). Precipitated solids were analyzed by means of the following techniques: laser diffraction (LD), focused-beam reflectance measurement (FBRM), scanning electron microscopy (SEM), and X-ray diffraction (XRD), in order to select a method for the determination of particle size of solids similar to scales, in order to study these deposits at the beginning of their formation and to evaluate the effect of additives in the scales particle size. Results were compared to those of scale deposits extracted from crude oil pipelines. SEM and XRD characterization showed that both the precipitation methods lead to calcium carbonate as a mixture of calcite, aragonite and vaterite, with rhombohedral morphology for method 1 and spherical for method 2. The effects of temperature, kinetics and Mg 2+ presence in the morphology of CaCO 3 were evaluated. Thus, the solids obtained by static bottle test and real scales are mainly formed by long needle-shaped aragonite. The comparison of the several particle size characterization methods determinates that an LD is a fast and sensitive technique for spherical and non-spherical solids, and it is a convenient technique for the analysis of scales extracted from oil pipelines.

  11. Deposition of calcium carbonate in karst caves: role of bacteria in Stiffe's cave.

    Directory of Open Access Journals (Sweden)

    Ercole Claudia

    2001-01-01

    Full Text Available Bacteria make a significant contribution to the accumulation of carbonate in several natural habitats where large amounts of carbonates are deposited. However, the role played by microbial communities in speleothem formation (stalactites, stalagmites etc. in caves is still unclear. In bacteria carbonate is formed by autotrophic pathways, which deplete CO2 from the environment, and by heterotrophic pathways, leading to active or passive precipitation. We isolated cultivable heterotrophic microbial strains, able to induce CaCO3 precipitation in vitro, from samples taken from speleothems in the galleries of Stiffe’s cave, L’Aquila, Italy. We found a large number of bacteria in the calcite formations (1 x 104 to 5 x 109 cells g-1. Microscopic examination, in laboratory conditions at different temperatures, showed that most of the isolates were able to form calcium carbonate microcrystals. The most crystalline precipitates were observed at 32°C. No precipitation was detected in un-inoculated controls media or in media that had been inoculated with autoclaved bacterial cells. X-ray diffraction (XRD analysis showed that most of the carbonate crystals produced were calcite. Bacillus strains were the most common calcifying isolates collected from Stiffe’s Cave. Analysis of carbonate-solubilization capability revealed that the non-calcifying bacteria were carbonate solubilizers.

  12. Carborane-Based Carbonic Anhydrase Inhibitors: Insight into CAII/CAIX Specificity from a High-Resolution Crystal Structure, Modeling, and Quantum Chemical Calculations

    Directory of Open Access Journals (Sweden)

    Pavel Mader

    2014-01-01

    Full Text Available Carborane-based compounds are promising lead structures for development of inhibitors of carbonic anhydrases (CAs. Here, we report structural and computational analysis applicable to structure-based design of carborane compounds with selectivity toward the cancer-specific CAIX isoenzyme. We determined the crystal structure of CAII in complex with 1-methylenesulfamide-1,2-dicarba-closo-dodecaborane at 1.0 Å resolution and used this structure to model the 1-methylenesulfamide-1,2-dicarba-closo-dodecaborane interactions with CAIX. A virtual glycine scan revealed the contributions of individual residues to the energy of binding of 1-methylenesulfamide-1,2-dicarba-closo-dodecaborane to CAII and CAIX, respectively.

  13. Carborane-Based Carbonic Anhydrase Inhibitors: Insight into CAII/CAIX Specificity from a High-Resolution Crystal Structure, Modeling, and Quantum Chemical Calculations

    Science.gov (United States)

    Mader, Pavel; Pecina, Adam; Cígler, Petr; Lepšík, Martin; Šícha, Václav; Hobza, Pavel; Grüner, Bohumír; Fanfrlík, Jindřich; Brynda, Jiří; Řezáčová, Pavlína

    2014-01-01

    Carborane-based compounds are promising lead structures for development of inhibitors of carbonic anhydrases (CAs). Here, we report structural and computational analysis applicable to structure-based design of carborane compounds with selectivity toward the cancer-specific CAIX isoenzyme. We determined the crystal structure of CAII in complex with 1-methylenesulfamide-1,2-dicarba-closo-dodecaborane at 1.0 Å resolution and used this structure to model the 1-methylenesulfamide-1,2-dicarba-closo-dodecaborane interactions with CAIX. A virtual glycine scan revealed the contributions of individual residues to the energy of binding of 1-methylenesulfamide-1,2-dicarba-closo-dodecaborane to CAII and CAIX, respectively. PMID:25309911

  14. The high contrast ratio and fast response time of a liquid crystal display lit by a carbon nanotube field emission backlight unit

    International Nuclear Information System (INIS)

    We report on the fabrication of a carbon nanotube field emission backlight unit (CNT-BLU) and its application for liquid crystal displays (LCD). The CNT-BLU was operated with locally controllable luminance and impulse-type scanning. The local luminance control, which is based on a very small block size of 1 cm2, consisted of local dimming and local brightening. This resulted in the contrast ratio of the LCD-TV to be as high as 300 000:1. A fast response time of ∼5.7 ms was also achieved from the LCD-TV lit by CNT-BLU, originating from the impulse-type scanning. In addition, the CNT-BLU showed long-term emission stability and high luminance uniformity

  15. Improvement of the relaxation time and the order parameter of nematic liquid crystal using a hybrid alignment mixture of carbon nanotube and polyimide

    International Nuclear Information System (INIS)

    We examined the electrooptical properties of a nematic liquid crystal (LC) sample whose substrates were coated with a mixture of carbon nanotube (CNT) and polyimide (PI). The relaxation time of the sample coated with 1.5 wt. % CNT mixture was about 35% reduced compared to the pure polyimide sample. The elastic constant and the order parameter of the CNT-mixture sample were increased and the fast relaxation of LC could be approximated to the mean-field theory. We found the CNT-mixed polyimide formed more smooth surface than the pure PI from atomic force microscopy images, indicating the increased order parameter is related to the smooth surface topology of the CNT-polyimide mixture

  16. Improvement of the relaxation time and the order parameter of nematic liquid crystal using a hybrid alignment mixture of carbon nanotube and polyimide

    Science.gov (United States)

    Lee, Hyojin; Yang, Seungbin; Lee, Ji-Hoon; Soo Park, Young

    2014-05-01

    We examined the electrooptical properties of a nematic liquid crystal (LC) sample whose substrates were coated with a mixture of carbon nanotube (CNT) and polyimide (PI). The relaxation time of the sample coated with 1.5 wt. % CNT mixture was about 35% reduced compared to the pure polyimide sample. The elastic constant and the order parameter of the CNT-mixture sample were increased and the fast relaxation of LC could be approximated to the mean-field theory. We found the CNT-mixed polyimide formed more smooth surface than the pure PI from atomic force microscopy images, indicating the increased order parameter is related to the smooth surface topology of the CNT-polyimide mixture.

  17. Improvement of the relaxation time and the order parameter of nematic liquid crystal using a hybrid alignment mixture of carbon nanotube and polyimide

    Energy Technology Data Exchange (ETDEWEB)

    Lee, Hyojin; Yang, Seungbin; Lee, Ji-Hoon, E-mail: jihoonlee@jbnu.ac.kr [Advanced Electronics and Information Research Center, Division of Electronic Engineering, Chonbuk National University, Jeonju, Jeonbuk 561-756 (Korea, Republic of); Soo Park, Young, E-mail: irony@kctech.re.kr [Department of Polymer-Nano Science and Technology, Chonbuk National University, Jeonju, Jeonbuk, 561-756 (Korea, Republic of); Korea Institute of Carbon Convergence Technology, Banryong-ro, Jeonju, Jeonbuk 561-844 (Korea, Republic of)

    2014-05-12

    We examined the electrooptical properties of a nematic liquid crystal (LC) sample whose substrates were coated with a mixture of carbon nanotube (CNT) and polyimide (PI). The relaxation time of the sample coated with 1.5 wt. % CNT mixture was about 35% reduced compared to the pure polyimide sample. The elastic constant and the order parameter of the CNT-mixture sample were increased and the fast relaxation of LC could be approximated to the mean-field theory. We found the CNT-mixed polyimide formed more smooth surface than the pure PI from atomic force microscopy images, indicating the increased order parameter is related to the smooth surface topology of the CNT-polyimide mixture.

  18. Measurement of solid precipitation with an optical disdrometer

    Science.gov (United States)

    Lempio, G. E.; Bumke, K.; Macke, A.

    2007-04-01

    A study about measurements of solid precipitation using an optical disdrometer is presented. The optical disdrometer is an improved version of the ODM 470 disdrometer. It allows to measure hydrometeors within a size range of 0.4 to 22 mm in diameter. The main advantage of this instrument is its ability to estimate accurately precipitation even under strong wind conditions (Großklaus, 1996). To measure solid precipitation a geometrical model was developed to determine the mean cross-sectional area of snow crystals for different predefined shapes and sizes. It serves to develop an algorithm, which relates the mean cross sectional area of snow crystals to their maximum dimension, liquid water content, and terminal velocity. The algorithm was applied to disdrometer measurements during winter 1999/2000 in Uppsala/Sweden. Resulting precipitation was compared to independent measurements of a Geonor gauge and to manual measurements. In terms of daily precipitation the disdrometer shows a reliable performance.

  19. Two-dimensional carbon crystals. Electrical transport in single- and double-layer graphene; Zweidimensionale Kohlenstoffkristalle. Elektrischer Transport in Einzel- und Doppellagen-Graphen

    Energy Technology Data Exchange (ETDEWEB)

    Schmidt, Hennrik

    2012-02-03

    In his work atomically thin layers of carbon, socalled graphene, are investigated. These systems exhibit outstanding electronic properties which are analysed using magnetotransport measurements. For this purpose, different types of samples are prepared, analysed and discussed. In addition to conventional single layer and single crystal bilayer systems, folded flakes with twisted planes are examined. Since monolayer graphene is a two dimensional crystal in which every atom sits at the surface, it is very sensitive to any type of perturbation. Three different cases are investigated: Firstly, dopants are removed from the surface and the change in transport properties is monitored. Secondly, the regime of small carrier concentrations is used to observe field induced recharging of inhomogeneities. Thirdly, an atomic force microscope is used to alter the graphene itself in a defined region. The implications of this modification are again investigated using magnetotransport measurements. The influence of one layer on another one is studied in decoupled two layer samples. A folded sample with separatly contacted layers is used to show transport through the folded region. For jointly contacted layers parallel transport measurements are performed to analyse screening effects of an applied electric field and substrate influence. The interaction of the two layers is shown by a significant reduction of the Fermivelocity.

  20. Purification, crystallization and preliminary X-ray analysis of urease from pigeon pea (Cajanus cajan)

    Energy Technology Data Exchange (ETDEWEB)

    Balasubramanian, Anuradha; Ponnuraj, Karthe, E-mail: pkarthe@hotmail.com [Centre of Advanced Study in Crystallography and Biophysics, University of Madras, Guindy Campus, Chennai 600 025 (India)

    2008-07-01

    Urease from pigeon pea was purified and crystallized and X-ray diffraction data were collected at 2.5 Å resolution. Urease is a seed protein that is common to most Leguminosae. It also occurs in many bacteria, fungi and several species of yeast. Urease catalyzes the hydrolysis of urea to ammonia and carbon dioxide, thus allowing organisms to use exogenous and internally generated urea as a nitrogen source. Urease from pigeon pea seeds has been purified to electrophoretic homogeneity using a series of steps involving ammonium sulfate fractionation, acid precipitation, ion-exchange and size-exclusion chromatography techniques. The pigeon pea urease was crystallized and the resulting crystals diffracted to 2.5 Å resolution. The crystals belong to the rhombohedral space group R32, with unit-cell parameters a = b = 176.29, c = 346.44 Å.

  1. High hydrogen loading of thin palladium wires through alkaline earth carbonates' precipitation on the cathodic surface - evidence of a new phase in the Pd-H system

    Energy Technology Data Exchange (ETDEWEB)

    Celani, F.; Spallone, A.; Di Gioacchino, D. [Istituto Nazionale di Fisica Nucleare, Laboratori Nazionali di Frascati, Frascati, RM (Italy); Marini, P.; Di Stefano, V.; Nakamura, M. [EURESYS, Rome (Italy); Pace, S. [Salerno Univ., Salerno (Italy). Dept. of Physics, Istituto Nazionale per la Fisica della Materia; Mancini, A. [ORIM S.r.l., Piediripa, MC (Italy); Tripodi, P. [Stanford Research Institut International, Stanford, CA (United States)

    2000-07-01

    A new protocol for the electrolytic loading of hydrogen (H) in thin palladium (Pd) wires has been developed. In order to increase the cathodic overvoltage, which is known to be the main parameter capable to enhance the electrolytic H loading of Pd, the catalytic action of the Pd surface versus H-H recombination has been strongly reduced by precipitation of a thin layer of alkaline-earth carbonates on the cathode. A set of electrolytes has been employed, containing small amounts of hydrochloric or sulfuric acid and strontium or calcium ions. The H loading has been continuously evaluated through ac measurements of the Pd wire resistance. Uncommonly low resistivity values, leading to an estimate of exceptionally high H loading, have been observed. Evidence of the existence of a new phase in the very high H content region of the Pd-H system has been inferred on the basis of the determination of the temperature coefficient of the electrical resistivity. Mainly for this purpose a thin layer of Hg was galvanically deposed on the cathodic surface, in order to prevent any H deloading during the measurements. The results have been fully reproduced in other 2 well equipped and experienced Laboratories (Italy, USA).

  2. Distinctive Accessory Minerals, Textures and Crystal Habits in Biofilm Associated Gypsum Deposits

    Science.gov (United States)

    Vogel, M.; Des Marais, D.; Jahnke, L.; Parenteau, M.

    2008-12-01

    Gypsum-depositing environments near Guerrero Negro, Baja California Sur, Mexico were investigated in order to differentiate the influence of microbial activity versus nonbiological processes upon sedimentary fabrics and minerals. Field sites were located in sabkhas (mudflats and anchialine pools) and in seawater concentration ponds in the salt production facility operated by Exportadora de Sal, S. A. Gypsum (CaSO4.2H2O) was classified according to sedimentary environment (e.g., mudflats, anchialine pools, saltern ponds, surface and subsurface sediments), sedimentary texture, mineral composition, crystal habit, brine composition and other geochemical and biological factors. Gypsum types that develop in the absence of biofilms include water column precipitates (pelagic grains) and subsedimentary crystalline discs that form from phreatic brine ripening. Subsedimentary gypsum forming in sabkha environments had a sinuous axial microtexture and poikilitically enclosed detrital particles whereas water column precipitates exhibited euhedral prismatic habits and extensive penetrative twinning. Gypsum that was influenced by biofilms included cumulate crusts and gypsooids / gypsolite developing in anchialine pools and in saltern concentration ponds. Gypsum precipitating within subaqueous benthic microbial mats, or biofilm/sediment surfaces offered compelling evidence of biofilm influence on crystal textures and habits. Biofilm effects include irregular high relief surface textures, accessory minerals (elemental sulfur, Ca-carbonate, Sr/Ca-sulfate, Mg-oxide and Mg- sulfate) and distinctive crystal habits. Elemental sulfur, Ca-carbonate, and Sr/Ca-sulfate are known byproducts of bacterially mediated sulfate reduction (BSR). Populations of gypsum crystals within biofilms exhibited euhedral to lensoidal morphologies with unique equant and distorted prismatic forms. These forms had been shown to arise from form- and face-specific inhibition by bioorganic functional groups (Cody

  3. Preparation of Calcined Zirconia-Carbon Composite from Metal Organic Frameworks and Its Application to Adsorption of Crystal Violet and Salicylic Acid

    Directory of Open Access Journals (Sweden)

    Zubair Hasan

    2016-03-01

    Full Text Available Zirconia-carbon (ZC composites were prepared via calcination of Zr-based metal organic frameworks, UiO-66 and amino-functionalized UiO-66, under N2 atmosphere. The prepared composites were characterized using a series of instrumental analyses. The surface area of the ZC composites increased with the increase of calcination temperature, with the formation of a graphite oxide phase observed at 900 °C. The composites were used for adsorptive removal of a dye (crystal violet, CV and a pharmaceutical and personal care product (salicylic acid, SA. The increase of the calcination temperature resulted in enhanced adsorption capability of the composites toward CV. The composite calcined at 900 °C exhibited a maximum uptake of 243 mg·g−1, which was much greater than that by a commercial activated carbon. The composite was also effective in SA adsorption (102 mg·g−1, and N-functionalization of the composite further enhanced its adsorption capability (109 mg·g−1. CV adsorption was weakly influenced by solution pH, but was more dependent on the surface area and pore volume of the ZC composite. Meanwhile, SA adsorption showed strong pH dependence, which implies an active role of electrostatic interactions in the adsorption process. Base-base repulsion and hydrogen bonding are also suggested to influence the adsorption of CV and SA, especially for the N-functionalized composite.

  4. 花生壳活性炭吸附染料废水中结晶紫的研究%Study on Adsorbing Crystal Violet from Dyeing Wastewater by Peanut Shell Active Carbon

    Institute of Scientific and Technical Information of China (English)

    张晋峰; 张莹琪

    2015-01-01

    利用磷酸处理微波照射制备花生壳活性炭,以一定浓度的结晶紫溶液为模拟染料废水,研究了吸附剂粒径、溶液pH值、结晶紫的初始浓度、吸附剂用量、吸附时间、吸附温度对结晶紫吸附性能的影响。结果表明花生壳活性炭是具有高去除率的廉价吸附剂,最大去除率达96%。结晶紫染料在花生壳活性炭上的吸附过程符合二级动力学模型和Freundlich等温吸附方程。%The peanut shell active carbon is prepared with phosphoric acid treatment and microwave irradiation and then is used as an adsorbent to adsorb crystal violet from aqueous solution ,which served as simulated dye waste water ,to study the influences of some factors ,including the particle size of the peanut shell active carbon ,pH ,initial concentration of crystal violet ,dosage of the peanut shell active carbon ,adsorption time and adsorption temperature ,on adsorptive property to crystal violet .The results show that the peanut shell active carbon is a kind effective and low cost adsorbent .The best removal rate of crystal violet is about 96% .The ad‐sorption process of the peanut shell active carbon with crystal violet follows the pseudo-second order kinetics model and Freundlich adsorption isotherm .

  5. A molecular dynamics study of the effect of thermal boundary conductance on thermal transport of ideal crystal of n-alkanes with different number of carbon atoms

    Science.gov (United States)

    Rastgarkafshgarkolaei, Rouzbeh; Zeng, Yi; Khodadadi, J. M.

    2016-05-01

    Phase change materials such as n-alkanes that exhibit desirable characteristics such as high latent heat, chemical stability, and negligible supercooling are widely used in thermal energy storage applications. However, n-alkanes have the drawback of low thermal conductivity values. The low thermal conductivity of n-alkanes is linked to formation of randomly oriented nano-domains of molecules in their solid structure that is responsible for excessive phonon scattering at the grain boundaries. Thus, understanding the thermal boundary conductance at the grain boundaries can be crucial for improving the effectiveness of thermal storage systems. The concept of the ideal crystal is proposed in this paper, which describes a simplified model such that all the nano-domains of long-chain n-alkanes are artificially aligned perfectly in one direction. In order to study thermal transport of the ideal crystal of long-chain n-alkanes, four (4) systems (C20H42, C24H50, C26H54, and C30H62) are investigated by the molecular dynamics simulations. Thermal boundary conductance between the layers of ideal crystals is determined using both non-equilibrium molecular dynamics (NEMD) and equilibrium molecular dynamics (EMD) simulations. Both NEMD and EMD simulations exhibit no significant change in thermal conductance with the molecular length. However, the values obtained from the EMD simulations are less than the values from NEMD simulations with the ratio being nearly three (3) in most cases. This difference is due to the nature of EMD simulations where all the phonons are assumed to be in equilibrium at the interface. Thermal conductivity of the n-alkanes in three structures including liquid, solid, and ideal crystal is investigated utilizing NEMD simulations. Our results exhibit a very slight rise in thermal conductivity values as the number of carbon atoms of the chain increases. The key understanding is that thermal transport can be significantly altered by how the molecules and the

  6. Precipitated magnetite in alpha effluent treatment

    International Nuclear Information System (INIS)

    Iron present as a fortuitous component of most nuclear plant effluents can be precipitated as magnetite after suitable chemical treatment. The spinel crystal lattice of the magnetite is able to incorporate a wide range of foreign ions which includes many important radioactive species. Provided the operating conditions are well chosen the precipitated magnetite provides an excellent scavenger for many radionuclides and gives a denser more granular solid product to be separated from the effluent than the more visual scavenging agent ferric hydroxide. The conditions under which magnetite can be formed by precipitation and its properties are presented and compared with those of ferric hydroxide. Because magnetite has a high magnetic susceptibility its separation by high gradient magnetic separation becomes a possibility and data relevant to this is presented. (author)

  7. 丝胶对碳酸钙晶体生长的调控作用研究%Study on the regulation and control of silk sericin on the crystal formation of Calcium Carbonate

    Institute of Scientific and Technical Information of China (English)

    丁少; 王海龙; 须苏菊; 孔祥东

    2012-01-01

    以水溶性丝胶为有机模板调控碳酸钙晶体生长,探讨了丝胶质量浓度差异对晶体生长的影响作用.采用场发射扫描电镜(FESEM)、X射线衍射(XRD)、红外光谱(FTIR)对所制备的样品进行表征.结果表明:通过控制丝胶质量浓度可调控碳酸钙的晶体生长,引起晶体形貌与尺寸的显著变化,并抑制碳酸钙特定晶面的生长.制备了刺球状碳酸钙和片层结构组装而成的类正方体碳酸钙,并对其形成机理进行了初步探讨,结果表明丝胶与无机晶体之间存在复杂的相互作用,丝胶对碳酸钙晶体的生长具有调制作用.%This study uses silk sericin as organic template to regulate the crystal formation of calcium carbonate in the presence of protein, discusses the mass concentration of silk sericin on the crystal growth. The obtained samples are characterized by field emission scanning electron microscopy (FESEM), X-ray diffraction (XRD), infrared spectroscopy (FTIR). The result shows that controlling the the mass concentration of silk sericin can regulate the crystal growth of calcium carbonate, significantly change the appearance and size of crystal and restrain the specific crystal growth of calcium carbonate. Cube-like calcium carbonate formed by thorn spherical calcium carbonate aggregates and lamellar structure was prepared, the formation mechanism of which is discussed preliminarily. The result shows that interaction between silk sericin and mineral crystal was very complex and silk sericin had a significant effect on the formation of calcium carbonate crystal.

  8. Nanometric inclusions of carbonates in Kokchetav diamonds from Kazakhstan: A new constraint for the depth of metamorphic diamond crystallization

    Science.gov (United States)

    Dobrzhinetskaya, Larissa F.; Wirth, Richard; Green, Harry W.

    2006-03-01

    Previous studies have revealed that microdiamonds from the Kokchetav ultra-high pressure metamorphic terrane of Kazakhstan contain nanometric scale inclusions of Si-, Fe-, Ti-, and Cr-oxides. Because the structure of SiO 2 inclusions was not confirmed to be coesite or stishovite due to their very small size, such diamonds formerly served only as an indicator of a minimum pressure, ca. 4 GPa. Geothermobarometry applied to Kokchetav diamond-bearing rocks yielded a wide range of conditions: T = 700 °C-1250 °C, and P = 4-9 GPa. Our paper presents transmission electron microscopy studies with focused ion beam assistance that indicate that diamonds from marbles contain inclusions of aragonite (CaCO 3) and magnesite (MgCO 3), and that aragonite and nitrogen-bearing nanometric particles are associated with dislocations reflecting diamond growth at relatively high-temperature conditions. We determined the boundary of dolomite stability using the reaction CaMg(CO 3) 2 (dolomite) = CaCO 3 (aragonite) + MgCO 3. This allowed us to utilize available experimental data to evaluate the pressure at which diamond was crystallized. Taking into consideration uncertainties existing between experimental data produced in different laboratories, we propose the pressure for Kokchetav diamond crystallization to be ˜ 6 to 9 GPa. This evaluation is based on the assumption that temperature was determined correctly as 980 °C (minimum) and 1250 °C (maximum) for diamond-grade dolomitic marbles. Our data provide strong evidence that the metasedimentary rocks of the Kokchetav massif containing diamonds were subducted to the depth of ˜ 190-280 km.

  9. Turning sunlight into stone: the oxalate-carbonate pathway in a tropical tree ecosystem

    Directory of Open Access Journals (Sweden)

    G. Cailleau

    2011-07-01

    Full Text Available An African oxalogenic tree, the iroko tree (Milicia excelsa, has the property to enhance carbonate precipitation in tropical oxisols, where such accumulations are not expected due to the acidic conditions in these types of soils. This uncommon process is linked to the oxalate-carbonate pathway, which increases soil pH through oxalate oxidation. In order to investigate the oxalate-carbonate pathway in the iroko system, fluxes of matter have been identified, described, and evaluated from field to microscopic scales. In the first centimeters of the soil profile, decaying of the organic matter allows the release of whewellite crystals, mainly due to the action of termites and saprophytic fungi. In addition, a concomitant flux of carbonate formed in wood tissues contributes to the carbonate flux and is identified as a direct consequence of wood feeding by termites. Nevertheless, calcite biomineralization of the tree is not a consequence of in situ oxalate consumption, but rather related to the oxalate oxidation inside the upper part of the soil. The consequence of this oxidation is the presence of carbonate ions in the soil solution pumped through the roots, leading to preferential mineralization of the roots and the trunk base. An ideal scenario for the iroko biomineralization and soil carbonate accumulation starts with oxalatization: as the iroko tree grows, the organic matter flux to the soil constitutes the litter, and an oxalate pool is formed on the forest ground. Then, wood rotting agents (mainly termites, saprophytic fungi, and bacteria release significant amounts of oxalate crystals from decaying plant tissues. In addition, some of these agents are themselves producers of oxalate (e.g. fungi. Both processes contribute to a soil pool of "available" oxalate crystals. Oxalate consumption by oxalotrophic bacteria can then start. Carbonate and calcium ions present in the soil solution represent the end products of the oxalate-carbonate

  10. Turning sunlight into stone: the oxalate-carbonate pathway in a tropical tree ecosystem

    Directory of Open Access Journals (Sweden)

    G. Cailleau

    2011-02-01

    Full Text Available An African oxalogenic tree, the iroko tree (Milicia excelsa, has the property to enhance carbonate precipitation in tropical oxisols, where such accumulations are not expected due to the theoretical acidic conditions of these soils. This uncommon process is linked to the oxalate-carbonate pathway, which increases soil pH through oxalate oxidation. In order to investigate the oxalate-carbonate pathway in the iroko system, fluxes of matter have been identified, described, and evaluated from field to microscopic scales. In the first centimeters of the soil profile, decaying of the organic matter allows the release of whewellite crystals, mainly due to the action of termites and saprophytic fungi. Regarding the carbonate flux, another direct consequence of wood feeding is a concomitant flux of carbonate formed in wood tissues, which is not consumed by termites. Nevertheless, calcite biomineralization of the tree is not a consequence of in situ oxalate consumption, but rather related to the oxalate oxidation inside the upper part of the soil. The consequence of this oxidation is the presence of carbonate ions in the soil solution pumped through the roots, leading to preferential mineralization of the roots and the trunk base. An ideal scenario for the iroko biomineralization and soil carbonate accumulation starts with oxalatization: as the iroko tree grows, the organic matter flux to the soil constitutes the litter. Therefore, an oxalate pool is formed on the forest ground. Then, wood rotting gents (mainly termites, fungi, and bacteria release significant amounts of oxalate crystals from decaying plant tissues. In addition some of these gents are themselves producers of oxalate (fungi. Both processes contribute to a soil pool of "available" oxalate crystals. Oxalate consumption by oxalotrophic bacteria can start. Carbonate and calcium ions present in the soil solution represent the end products of the oxalate-carbonate pathway. The solution is pumped

  11. Turning sunlight into stone: the oxalate-carbonate pathway in a tropical tree ecosystem

    Science.gov (United States)

    Cailleau, G.; Braissant, O.; Verrecchia, E. P.

    2011-07-01

    An African oxalogenic tree, the iroko tree (Milicia excelsa), has the property to enhance carbonate precipitation in tropical oxisols, where such accumulations are not expected due to the acidic conditions in these types of soils. This uncommon process is linked to the oxalate-carbonate pathway, which increases soil pH through oxalate oxidation. In order to investigate the oxalate-carbonate pathway in the iroko system, fluxes of matter have been identified, described, and evaluated from field to microscopic scales. In the first centimeters of the soil profile, decaying of the organic matter allows the release of whewellite crystals, mainly due to the action of termites and saprophytic fungi. In addition, a concomitant flux of carbonate formed in wood tissues contributes to the carbonate flux and is identified as a direct consequence of wood feeding by termites. Nevertheless, calcite biomineralization of the tree is not a consequence of in situ oxalate consumption, but rather related to the oxalate oxidation inside the upper part of the soil. The consequence of this oxidation is the presence of carbonate ions in the soil solution pumped through the roots, leading to preferential mineralization of the roots and the trunk base. An ideal scenario for the iroko biomineralization and soil carbonate accumulation starts with oxalatization: as the iroko tree grows, the organic matter flux to the soil constitutes the litter, and an oxalate pool is formed on the forest ground. Then, wood rotting agents (mainly termites, saprophytic fungi, and bacteria) release significant amounts of oxalate crystals from decaying plant tissues. In addition, some of these agents are themselves producers of oxalate (e.g. fungi). Both processes contribute to a soil pool of "available" oxalate crystals. Oxalate consumption by oxalotrophic bacteria can then start. Carbonate and calcium ions present in the soil solution represent the end products of the oxalate-carbonate pathway. The solution is

  12. Shallow burial dolomitisation of Middle-Upper Permian paleosols in an extensional tectonic context (SE Iberian Basin, Spain): Controls on temperature of precipitation and source of fluids

    Science.gov (United States)

    Benito, M. Isabel; De la Horra, Raúl; López-Gómez, José; Barrenechea, José F.; Luque, Javier; Arche, Alfredo

    2011-06-01

    This work is focused on carbonate paleosols developed in three stratigraphic sections (Landete, Talayuelas and Henarejos) of the Middle-Late Permian Alcotas Formation in the SE Iberian Basin. The Alcotas Formation, of alluvial origin, was deposited in semi-connected half-grabens developed during the early stages of the Permian-Triassic rifting stage that affected the Iberian Basin. The studied sections were located in two of these half-grabens, the Henarejos section being much closer to the basin boundary fault than the other two sections. The mineralogy and texture of the carbonate precursor of paleosols in the three studied sections are not preserved because original carbonate is replaced by coarse crystals of dolomite and/or magnesite. Dolomite crystals are typically euhedral, displaying rhombohedral shapes and reddish luminescence, although in the Henarejos section dolomite displays non-planar boundaries and frequently saddle habit. Micas are deformed and adapted to dolomite crystals, which, in turn, are affected by stylolites, suggesting that dolomite precipitated before mechanical and chemical compaction. Carbon and oxygen isotopic compositions of dolomite from the three sections show different values (δ 13C VPDB mean values = - 6.7‰, - 5.5‰ and - 7.5‰; δ 18O VPDB mean values = - 4.0‰; -5.6‰ and - 8.2‰, at Landete, Talayuelas and Henarejos sections, respectively). The 87Sr/ 86Sr ratios are similar in the three sections yielding values between 0.71391 and 0.72213. The petrographic and geochemical features of dolomite in the three studied sections suggest precipitation from similar fluids and during shallow burial diagenesis. Assuming that the minimum temperature for dolomite precipitation in the Henarejos section was 60 °C (as suggested by the presence of non-planar saddle habit), and that the dolomitizing fluid had similar δ 18O values at the three localities, then dolomite in the Talayuelas and Landete sections precipitated at temperatures

  13. WPA Precipitation Tabulations

    Data.gov (United States)

    National Oceanic and Atmospheric Administration, Department of Commerce — Hourly precipitation data tabulated under the Work Projects Administration (WPA), a New Deal program created to reduce unemployment during the Great Depression....

  14. Chemisorption And Precipitation Reactions

    Science.gov (United States)

    The transport and bioavailability of chemical components within soils is, in part, controlled by partitioning between solids and solution. General terms used to describe these partitioning reactions include chemisorption and precipitation. Chemisorption is inclusive of the suit...

  15. Storage Gage Precipitation Observations

    Data.gov (United States)

    National Oceanic and Atmospheric Administration, Department of Commerce — A storage gage is a precipitation gage that requires reading and maintenance only monthly or seasonal intervals. This library includes reports from such gages,...

  16. Effects of nitrogen addition and precipitation change on soil methane and carbon dioxide fluxes%施氮和降水格局改变对土壤CH4和CO2通量的影响

    Institute of Scientific and Technical Information of China (English)

    李伟; 白娥; 李善龙; 孙建飞; 彭勃; 姜萍

    2013-01-01

    ,and even,converted the CH4 consumption into CH4 release.However,this inhibition effect only lasted for approximately 5 days.Nitrogen addition also affected the relationships between the CH4 flux and environmental factors (soil temperature,pH,and clay content) to some extent.The changed precipitation regime had no significant effects on the CH4 flux.Nitrogen addition decreased the CO2 flux,with an average decrement of 27.4% after 4 years continuous nitrogen addition.It was predicted that the effects of long-term continuous nitrogen addition on the CO2 flux would be increased with time,and reached the maximum after certain years of nitrogen addition.Oppositely,the effects of single time nitrogen addition would be decreased with time,and disappeared by the end of the 1-month cycle.The inhibition effect of nitrogen addition on the CO2 flux was negatively correlated with soil water filled pore space (WFPS) (P =0.022),and enhanced and extended at higher temperature.Nitrogen addition and precipitation change could possibly alter the temperature sensitivity of soil respiration.Our results indicated that the soil nitrogen in temperate forest in Changbai Mountains had not reached a threshold,and the future nitrogen deposition increase would inhibit the CO2 release and CH4 uptake.Overall,nitrogen addition would inhibit the soil carbon release.

  17. Precipitation response to regional radiative forcing

    Directory of Open Access Journals (Sweden)

    D. T. Shindell

    2012-02-01

    Full Text Available Precipitation shifts can have large impacts on human society and ecosystems. Many aspects of how inhomogeneous radiative forcings influence precipitation remain unclear, however. Here we investigate regional precipitation responses to various forcings imposed in different latitude bands in a climate model. We find that several regions show strong, significant responses to most forcings, but the magnitude and even the sign depends upon the forcing location and type. Aerosol and ozone forcings typically induce larger responses than equivalent carbon dioxide (CO2 forcing, and the influence of remote forcings often outweighs that of local forcings. Consistent with this, ozone and especially aerosols contribute greatly to precipitation changes over the Sahel and South and East Asia in historical simulations, and inclusion of aerosols greatly increases the agreement with observed trends in these areas, which cannot be attributed to either greenhouse gases or natural forcings. Estimates of precipitation responses derived from multiplying our Regional Precipitation Potential (RPP; the response per unit forcing relationships by historical forcings typically capture the actual response in full transient climate simulations fairly well, suggesting that these relationships may provide useful metrics. The strong sensitivity to aerosol and ozone forcing suggests that although some air quality improvements may unmask greenhouse gas-induced changes in temperature, they have large benefits for reducing regional disruption of the hydrologic cycle.

  18. Precipitation response to regional radiative forcing

    Directory of Open Access Journals (Sweden)

    D. T. Shindell

    2012-08-01

    Full Text Available Precipitation shifts can have large impacts on human society and ecosystems. Many aspects of how inhomogeneous radiative forcings influence precipitation remain unclear, however. Here we investigate regional precipitation responses to various forcings imposed in different latitude bands in a climate model. We find that several regions show strong, significant responses to most forcings, but that the magnitude and even the sign depends upon the forcing location and type. Aerosol and ozone forcings typically induce larger responses than equivalent carbon dioxide (CO2 forcing, and the influence of remote forcings often outweighs that of local forcings. Consistent with this, ozone and especially aerosols contribute greatly to precipitation changes over the Sahel and South and East Asia in historical simulations, and inclusion of aerosols greatly increases the agreement with observed trends in these areas, which cannot be attributed to either greenhouse gases or natural forcings. Estimates of precipitation responses derived from multiplying our Regional Precipitation Potentials (RPP; the response per unit forcing relationships by historical forcings typically capture the actual response in full transient climate simulations fairly well, suggesting that these relationships may provide useful metrics. The strong sensitivity to aerosol and ozone forcing suggests that although some air quality improvements may unmask greenhouse gas-induced warming, they have large benefits for reducing regional disruption of the hydrologic cycle.

  19. A living cell quartz crystal microbalance biosensor for continuous monitoring of cytotoxic responses of macrophages to single-walled carbon nanotubes

    Directory of Open Access Journals (Sweden)

    Marx Kenneth A

    2011-01-01

    Full Text Available Abstract Background Numerous engineered nanomaterials (ENMs exist and new ENMs are being developed. A challenge to nanotoxicology and environmental health and safety is evaluating toxicity of ENMs before they become widely utilized. Cellular assays remain the predominant test platform yet these methods are limited by using discrete time endpoints and reliance on organic dyes, vulnerable to interference from ENMs. Label-free, continuous, rapid response systems with biologically meaningful endpoints are needed. We have developed a device to detect and monitor in real time responses of living cells to ENMs. The device, a living cell quartz crystal microbalance biosensor (QCMB, uses macrophages adherent to a quartz crystal. The communal response of macrophages to treatments is monitored continuously as changes in crystal oscillation frequency (Δf. We report the ability of this QCMB to distinguish benign from toxic exposures and reveal unique kinetic information about cellular responses to varying doses of single-walled carbon nanotubes (SWCNTs. Results We analyzed macrophage responses to additions of Zymosan A, polystyrene beads (PBs (benign substances or SWCNT (3-150 μg/ml in the QCMB over 18 hrs. In parallel, toxicity was monitored over 24/48 hrs using conventional viability assays and histological stains to detect apoptosis. In the QCMB, a stable unchanging oscillation frequency occurred when cells alone, Zymosan A alone, PBs alone or SWCNTs without cells at the highest dose alone were used. With living cells in the QCMB, when Zymosan A, PBs or SWCNTs were added, a significant decrease in frequency occurred from 1-6 hrs. For SWCNTs, this Δf was dose-dependent. From 6-18 hrs, benign substances or low dose SWCNT (3-30 μg/ml treatments showed a reversal of the decrease of oscillation frequency, returning to or exceeding pre-treatment levels. Cell recovery was confirmed in conventional assays. The lag time to see the Δf reversal in QCMB plots

  20. Solvothermal synthesis of spherical YAG powders via different precipitants

    Energy Technology Data Exchange (ETDEWEB)

    Wu Zuogui [Department of Materials Science and Engineering, Shandong Institute of Light Industry, Jinan, Shandong 250353 (China); Zhang Xudong [Department of Materials Science and Engineering, Shandong Institute of Light Industry, Jinan, Shandong 250353 (China)], E-mail: wuzuogui11550@163.com; He Wen; Du Yuanwei; Jia Naitao; Liu Pengcheng; Bu Fanqing [Department of Materials Science and Engineering, Shandong Institute of Light Industry, Jinan, Shandong 250353 (China)

    2009-03-20

    Yttrium aluminum garnet (YAG) powders were synthesized by a solvothermal method under mild conditions with inexpensive aluminum and yttrium nitrates as the starting materials, and the ethylenediamine (EDA) solution as the solvent. Hydroxide precursors were synthesized by two different precipitating processes, in which urea or ammonium hydrogen carbonate was used as precipitant. The formation of YAG particle was investigated by means of Fourier transform infrared spectroscopy (FT-IR), X-ray diffraction (XRD) and transmission electron microscopy (TEM). The TEM results showed that spherical YAG powders were successfully synthesized when ammonium hydrogen carbonate was used as precipitant.

  1. Modern trends in technical crystallization

    Science.gov (United States)

    Matz, G.

    1980-04-01

    Interesting and significant developments have occurred in the last decade in both crystallization equipment and in the theory of crystallization process. In the field of technical crystallization new crystallizers have been developed and computer modelling has become important in scaling up and in the achievement of increased performance. The DP-Kristaller developed by Escher-Wyss-Tsukishima, the Brodie purifier, the sieve tray column having dancing balls, the automated multiple crystallization process due to Mützenberg and Saxer and the double belt cooler, all of which represent technical developments, are described in the first section. The second part of the paper reviews computer modelling of the fluidized bed crystallizer, chemical precipitation, flaking and prilling. Finally, there is a brief discussion of the impact of technical crystallization processes on environmental protection.

  2. Kinetics of niobium carbide precipitation in ferrite

    International Nuclear Information System (INIS)

    The aim of this study is to develop a NbC precipitation modelling in ferrite. This theoretical study is motivated by the fact it considers a ternary system and focus on the concurrence of two different diffusion mechanisms. An experimental study with TEP, SANS and Vickers micro-hardening measurements allows a description of the NbC precipitation kinetics. The mean radius of the precipitates is characterized by TEM observations. To focus on the nucleation stage, we use the Tomographic Atom Probe that analyses, at an atomistic scale, the position of the solute atoms in the matrix. A first model based on the classical nucleation theory and the diffusion-limited growth describes the precipitation of spherical precipitates. To solve the set of equations, we use a numerical algorithm that furnishes an evaluation of the precipitated fraction, the mean radius and the whole size distribution of the particles. The parameters that are the interface energy, the solubility product and the diffusion coefficients are fitted with the data available in the literature and our experimental results. It allows a satisfactory agreement as regards to the simplicity of the model. Monte Carlo simulations are used to describe the evolution of a ternary alloy Fe-Nb-C on a cubic centred rigid lattice with vacancy and interstitial mechanisms. This is realized with an atomistic description of the atoms jumps and their related frequencies. The model parameters are fitted with phase diagrams and diffusion coefficients. For the sake of simplicity, we consider that the precipitation of NbC is totally coherent and we neglect any elastic strain effect. We can observe different kinetic paths: for low supersaturations, we find an expected precipitation of NbC but for higher supersaturations, the very fast diffusivity of carbon atoms conducts to the nucleation of iron carbide particles. We establish that the occurrence of this second phenomenon depends on the vacancy arrival kinetics and can be related

  3. Calcite Supersaturation and Precipitation Kinetics in the Lower Colorado River, Ail-American Canal and East Highline Canal

    Science.gov (United States)

    Suarez, D. L.

    1983-06-01

    In situ pH determinations and analysis of major ions in solution indicated that the lower Colorado River is supersaturated with respect to calcite throughout the entire daily cycle, in both winter and summer. Although the ion activity product was 4 to 6 times greater than the calcite solubility product, there was no detectable precipitation. Chemical analyses of water samples taken along 350 km of the river and canals from Parker Dam to the Salton Sea also revealed no evidence of calcium carbonate precipitation despite the inflow of saline and highly supersaturated irrigation return flows. Laboratory kinetic studies indicated that calcite crystal growth rates with Colorado River water are about 30% of the rate for pure Ca-HCO3 waters and about 70% of that for synthetic Colorado River water. Calcite precipitation by crystal growth in the river is limited by the combination of short residence times and unavailability of reactive calcite. Critical supersaturation levels necessary for heterogeneous nucleation do not occur; a high suspended load limits algal photosynthesis and thus prevents large decreases in daytime H2CO3 levels.

  4. The Frontier Between Adsorption and Precipitation of Polyacrylic Acid on Calcium Carbonate Frontière entre adsorption et précipitation de l'acide polyacrylique sur le carbonate de calcium

    Directory of Open Access Journals (Sweden)

    Cabane B.

    2006-12-01

    Full Text Available Adsorption of polymers on mineral surfaces allowing colloidal stability have widespread applications in industrial processes. The binding mechanism has been quite well described on oxide surfaces. Mainly in terms of hydrogen bonds and electrostatic interactions between charged sites and polymer segments. This phenomenon has been modelized and the influence of pH. Ionic strentgh, and molecular weight can be calculated or predicted. In the case of sparingly soluble substrates such as BaSO4, CaCO3 or CaSO4, several problems arise : the difficulty for the identification of surface sites and the interference of ions coming from the material's solubility. In the case of calcite, the solubility imposes dissolved calcium ions in solution which could complex the polyelectrolyte and reduce its solubility. For that purpose, we have measured the binding energy using microcalorimetry. Microcalorimetric measurements have shown that the adsorption enthalpy is weakly enclothermic: about + 2 kj/mol. Interestingly, this value is very closed to that of calcium complexation with PANa. It is suggested that the driving force for adsorption is the net gain in entropy of the system. The microcalorimetric adsorption isotherm does not show any evidence for a strongly exothermic interaction between positive edges and negative segment of the polyion. Practically, in most cases, adsorption of polymers is calculated from the decrease of its concentration in the solution after separation of the solid by centrifugation. This procedure does not discriminate therefore between real adsorption and phase separation. To answer the question, we have performed adsorption experiments using a dialysis membrane to separate the solid particles from the solution. It has been established that in some circumstances, depending on the relative amount of calcite, calcium ions and polyelectrolyte, precipitation takes place rather than adsorption. This is especially the case at low polymer

  5. The potential for phosphorus pollution remediation by calcite precipitation in UK freshwaters

    Directory of Open Access Journals (Sweden)

    C. Neal

    2001-01-01

    Full Text Available This paper examines the potential for calcium carbonate to reduce phosphate pollution in freshwaters by co-precipitation, a process known as a "self cleansing mechanism". Calcium carbonate saturation levels and phosphate concentrations (SRP - soluble reactive phosphate across the major eastern UK river basins are examined to test for solubility controls. The study shows that calcite saturation varies for each catchment as a function of flow and biological activity rather than by direct regulation by SRP. Indeed, there is no evidence, for any of the rivers studied, that calcite solubility controls hold. However, for groundwater and groundwater-fed springs in the Chalk of the Thames basin, calcite saturation is observed with associated low SRP levels. A self-cleansing mechanism may well be operative within the Chalk due to two factors. Firstly, there is a high potential for nucleation on the calcite micro-crystals in the aquifer. Secondly, there are within aquifer reactions that remove the calcite nucleating inhibitors (SRP and dissolved organic carbon, DOC to levels lower than those occurring within the rivers do. These inhibitors enter the catchment at very high concentrations in association with agricultural pollution (fertilizer application and animal slurry and household contamination (e.g. sewage sources from septic tanks. Under low flow conditions, when the saturation index for calcite is at its highest, so too is the concentration of the nucleation inhibitor SRP. Companion work shows that calcite precipitation can occur at the water-sediment interface of the river and this may involve SRP removal. The data, as a whole, define an apparent bound for calcite solubility control where in the presence of nucleating centres, SRP must be less than 4 mM-P l-1 and DOC must be less than 150 mM-C l-1: a condition that does not seem to pertain within most UK rivers. Keywords: calcite, calcium carbonate, phosphate, soluble reactive phosphate, dissolved

  6. Precipitation chemistry in central Amazonia

    Science.gov (United States)

    Andreae, M. O.; Talbot, R. W.; Berresheim, H.; Beecher, K. M.

    1990-01-01

    Rain samples from three sites in central Amazonia were collected over a period of 6 weeks during the 1987 wet season and analyzed for ionic species and dissolved organic carbon. A continuous record of precipitation chemistry and amount was obtained at two of these sites, which were free from local or regional pollution, for a time period of over 1 month. The volume-weighted mean concentrations of most species were found to be about a factor of 5 lower during the wet season compared with previous results from the dry season. Only sodium, potassium, and chloride showed similar concentrations in both seasons. When the seasonal difference in rainfall amount is taken into consideration, the deposition fluxes are only slightly lower for most species during the wet season than during the dry season, again with the exception of chloride, potassium, and sodium. Sodium and chloride are present in the same ratio as in sea salt; rapid advection of air masses of marine origin to the central Amazon Basin during the wet season may be responsible for the observed higher deposition flux of these species. Statistical analysis suggests that sulfate is, to a large extent, of marine (sea salt and biogenic) origin, but that long-range transport of combustion-derived aerosols also makes a significant contribution to sulfate and nitrate levels in Amazonian rain. Organic acid concentrations in rain were responsible for a large fraction of the observed precipitation acidity; their concentration was strongly influenced by gas/liquid interactions.

  7. Electric double-layer capacitors with tea waste derived activated carbon electrodes and plastic crystal based flexible gel polymer electrolytes

    Science.gov (United States)

    Suleman, M.; Deraman, M.; Othman, M. A. R.; Omar, R.; Hashim, M. A.; Basri, N. H.; Nor, N. S. M.; Dolah, B. N. M.; Hanappi, M. F. Y. M.; Hamdan, E.; Sazali, N. E. S.; Tajuddin, N. S. M.; Jasni, M. R. M.

    2016-08-01

    We report a novel configuration of symmetrical electric double-layer capacitors (EDLCs) comprising a plastic crystalline succinonitrile (SN) based flexible polymer gel electrolyte, incorporated with sodium trifluoromethane sulfonate (NaTf) immobilised in a host polymer poly (vinylidine fluoride-co-hexafluoropropylene) (PVdF-HFP). The cost-effective activated carbon powder possessing a specific surface area (SSA) of ~ 1700 m2g-1 containing a large proportion of meso-porosity has been derived from tea waste to use as supercapacitor electrodes. The high ionic conductivity (~3.6×10-3 S cm-1 at room temperature) and good electrochemical stability render the gel polymer electrolyte film a suitable candidate for the fabrication of EDLCs. The performance of the EDLCs has been tested by electrochemical impedance spectroscopy (EIS), cyclic voltammetry (CV), and galvanostatic charge-discharge studies. The performance of the EDLC cell is found to be promising in terms of high values of specific capacitance (~270 F g-1), specific energy (~ 36 Wh kg-1), and power density (~ 33 kW kg-1).

  8. Rabi Wave Packets and Peculiarities of Raman Scattering in Carbon Nanotubes, Produced by High Energy Ion Beam Modification of Diamond Single Crystals

    CERN Document Server

    Yearchuck, Dmitry

    2011-01-01

    QED-model for multichain coupled qubit system, proposed in \\cite{Part1}, was confirmed by Raman scattering studies of quasi-1D carbon zigzag-shaped nanotubes (CZSNTs), produced by high energy ion beam modification of natural diamond single crystals. Multichain coupled qubit system represents itself Su-Schriffer-Heeger $\\sigma$-polaron lattice, formed in CZSNTs plus quantized external electromagnetic (EM) field. New quantum optics phenomenon - Rabi waves, predicted in \\cite{Slepyan_Yerchak} has experimentally been identified for the first time. It is shown, that Raman spectra in quasi-1D CZSNTs are quite different in comparison with well known Raman spectra in 2D those ones. They characterized by semiclassical consideration by the only one vibronic mode of Su-Schriffer-Heeger $\\sigma$-polaron lattice instead of longitudinal and transverse optical phonon $G^+$ and $G^-$modes and the out-of-plane radial breathing mode, which are observed in Raman spectra of 2D single wall nanotubes. It is consequence of 2D - 1D ...

  9. TEM investigations of fine niobium precipitates in HSLA steel

    Energy Technology Data Exchange (ETDEWEB)

    Beres, M.; Weirich, T.E.; Mayer, J. [Gemeinschaftslabor fuer Elektronenmikroskopie (GFE), RWTH Aachen, Aachen (Germany); Hulka, K. [Niobium Products Co. GmbH, Duesseldorf (Germany)

    2004-11-01

    Commercially produced 0.03% C, 0.08% Nb, 0.01% Ti high strength low alloyed (HSLA) steel in the form of 20 mm thick plates was investigated. The steel was thermomechanically processed and the mechanical properties of the steel were evaluated by tensile testing. Using analytical and high resolution transmission electron microscopy the distribution, morphology, composition, crystal structure and particle size of niobium and titanium carbonitrides were observed and identified in these steels. The distribution of the precipitates was found to be nearly random, with occasional occurrence of precipitation free zones. Complex agglomerates with a cubic TiN seed crystal overgrown by a cubic NbC particle were the most commonly observed precipitates. Further TEM analysis in the accelerated cooled and tempered specimens in 1/4 plate thickness did not reveal any evidence that additional precipitation in the ferrite occurred. Precipitation in ferrite was only detected after subsequent cold deformation and tempering of the same samples. By a combination of EFTEM, STEM, HRTEM in addition to EDX spectroscopy, a large population of strain induced NbC precipitates with fcc crystal structure ranging in size down to 2 nm were identified in the ferrite matrix. (orig.)

  10. Crystal Structures of Two Bacterial 3-Hydroxy-3-methylglutaryl-CoA Lyases Suggest a Common Catalytic Mechanism among a Family of TIM Barrel Metalloenzymes Cleaving Carbon-Carbon Bonds

    Energy Technology Data Exchange (ETDEWEB)

    Forouhar,F.; Hussain, M.; Farid, R.; Benach, J.; Abashidze, M.; Edstrom, W.; Vorobiev, S.; Montelione, G.; Hunt, J.; et al.

    2006-01-01

    The enzyme 3-hydroxy-3-methylglutaryl-coenzyme A (HMG-CoA) lyase catalyzes the terminal steps in ketone body generation and leucine degradation. Mutations in this enzyme cause a human autosomal recessive disorder called primary metabolic aciduria, which typically kills victims because of an inability to tolerate hypoglycemia. Here we present crystal structures of the HMG-CoA lyases from Bacillus subtilis and Brucella melitensis at 2.7 and 2.3 {angstrom} resolution, respectively. These enzymes share greater than 45% sequence identity with the human orthologue. Although the enzyme has the anticipated triose-phosphate isomerase (TIM) barrel fold, the catalytic center contains a divalent cation-binding site formed by a cluster of invariant residues that cap the core of the barrel, contrary to the predictions of homology models. Surprisingly, the residues forming this cation-binding site and most of their interaction partners are shared with three other TIM barrel enzymes that catalyze diverse carbon-carbon bond cleavage reactions believed to proceed through enolate intermediates (4-hydroxy-2-ketovalerate aldolase, 2-isopropylmalate synthase, and transcarboxylase 5S). We propose the name 'DRE-TIM metallolyases' for this newly identified enzyme family likely to employ a common catalytic reaction mechanism involving an invariant Asp-Arg-Glu (DRE) triplet. The Asp ligates the divalent cation, while the Arg probably stabilizes charge accumulation in the enolate intermediate, and the Glu maintains the precise structural alignment of the Asp and Arg. We propose a detailed model for the catalytic reaction mechanism of HMG-CoA lyase based on the examination of previously reported product complexes of other DRE-TIM metallolyases and induced fit substrate docking studies conducted using the crystal structure of human HMG-CoA lyase (reported in the accompanying paper by Fu, et al. (2006) J. Biol. Chem. 281, 7526-7532). Our model is consistent with extensive mutagenesis

  11. Heterogeneous growth of cadmium and cobalt carbonate phases at the (101¯4) calcite surface

    Energy Technology Data Exchange (ETDEWEB)

    Xu, Man; Ilton, Eugene S.; Engelhard, Mark H.; Qafoku, Odeta; Felmy, Andrew R.; Rosso, Kevin M.; Kerisit, Sebastien N.

    2015-03-01

    The ability of surface precipitates to form heteroepitaxially is an important factor that controls the extent of heterogeneous growth. In this work, the growth of cadmium and cobalt carbonate phases on (10-14) calcite surfaces is compared for a range of initial saturation states with respect to otavite (CdCO3) and sphaerocobaltite (CoCO3), two isostructural metal carbonates that exhibit different lattice misfits with respect to calcite. Calcite single crystals were reacted in static conditions for 16 hours with CdCl2 and CoCl2 aqueous solutions with initial concentrations 0.3 ≤ [Cd2+]0 ≤ 100 μM and 25 ≤ [Co2+]0 ≤ 200 μM. The reacted crystals were imaged in situ with atomic force microscopy (AFM) and analyzed ex situ with X-ray photoelectron spectroscopy (XPS). AFM images of Cd-reacted crystals showed the formation of large islands elongated along the direction, clear evidence of heteroepitaxial growth, whereas surface precipitates on Co-reacted crystals were small round islands. Deformation of calcite etch pits in both cases indicated the incorporation of Cd and Co at step edges. XPS analysis pointed to the formation of a Cd-rich (Ca,Cd)CO3 solid solution coating atop the calcite substrate. In contrast, XPS measurements of the Co-reacted crystals provided evidence for the formation of a mixed hydroxy-carbonate cobalt phase. The combined AFM and XPS results suggest that the lattice misfit between CoCO3 and CaCO3 ( 15% based on surface areas) is too large to allow for heteroepitaxial growth of a pure cobalt carbonate phase on calcite surfaces in aqueous solutions and at ambient conditions. The use of the satellite structure of the Co 2p3/2 photoelectron line as a tool for determining the nature of cobalt surface precipitates is also discussed.

  12. Precipitating factors of asthma.

    Science.gov (United States)

    Lee, T H

    1992-01-01

    Asthma is characterised by bronchial hyperresponsiveness. This feature of the asthmatic diathesis predisposes patients to wheezing in response to a number of different factors. These precipitating factors include specific allergen acting via sensitised mediator cells through an IgE-dependent mechanism. There are irritants which may work through a non-specific manner, or stimuli such as exercise and hyperventilation, which probably also act through mediator release via a non-IgE-dependent manner. The mechanism whereby physical stimuli such as exercise induce bronchoconstriction is of interest, because it increases the context in which the mast cell may participate in acute asthmatic bronchoconstriction. Respiratory infections also commonly provoke asthma, especially in infants and may, indeed, precipitate the asthmatic state itself. Finally, drugs can often trigger asthma attacks and the mechanisms of asthma precipitated by non-steroidal anti-inflammatory drugs such as aspirin have been the subject of recent research.

  13. From precipitation to stream

    OpenAIRE

    Peralta-Tapia, Andres

    2015-01-01

    Understanding the journey water makes from precipitation entering a catchment, traveling through soils, and the time it takes before it exits as stream water are questions of great relevance for both scientists and environmental managers. Natural stable isotopes such as δ¹⁸O and δ²H have been extensively used over the last decades to trace water through diverse catchments across the world. In this thesis I analyzed over 2500 isotope samples to create long-term time series of precipitation and...

  14. Analysis of microalloy precipitate reversion in steels

    Science.gov (United States)

    Michal, G. M.; Locci, I. E.

    1988-01-01

    The influence of the ferrite to austenite allotropic transformation on the stability of MXn precipitates in an iron matrix is studied. In the MX phase, M is a group IVb or Vb transition metal, such as niobium, titanium, or vanadium. X is carbon or nitrogen and n is in the range of 0.75-1.0. The application of the present model to the case of vanadium carbide reversion in a microalloyed steel is discussed.

  15. Nanoscale precipitation in hot rolled sheet steel

    Science.gov (United States)

    Sun, Jun

    Some newer hot rolled high strength low alloy (HSLA) steels with a single phase ferrite matrix have obtained substantial strengthening from nanoscale precipitation. These HSLA are reported to have a good combination of strength, ductility and hole-expansion ability. In the current work, Gleeble ® 3500 torsion testing was employed to simulate the hot rolling process with varying run-out table cooling rates and coiling temperatures on five microalloyed steels with additions of Ti, Nb, Mo, Cr and V, to investigate the effects of microalloy additions and processing conditions on microstructures as well as mechanical properties. Subsized tensile specimens obtained from as-twisted torsion samples were used to evaluate mechanical properties. The precipitation states of the five steels with different processing conditions were characterized using extraction replica TEM. Comparison of microstructures and mechanical properties was discussed. Characterization of the microstructure via light optical microscopy showed the matrix microstructure was mainly influenced by coiling temperature, which indicates that the transformation from austenite to ferrite occurred during the coiling period. A higher Ti content was shown to reduce the second constituent fractions. Investigation of carbon extraction replica specimens via TEM revealed the presence of nanoscale precipitation. Extensive nanoscale precipitation was observed in most of the specimens having a polygonal ferrite matrix, while in the granular bainite/ferrite microstructure at lower temperatures, fewer microalloy carbides were present. The specimens with polygonal ferrite had similar or higher yield strength than the specimens with granular bainite microstructure, which suggests the effectiveness of precipitation strengthening from extensive nanoscale precipitates. In the Nb-Mo steel, more significant strengthening due to grain refinement was evident. Yield strength values were less than reported for JFE's "NANOHITEN

  16. Predicting cement distribution in geothermal sandstone reservoirs based on estimates of precipitation temperatures

    Science.gov (United States)

    Olivarius, Mette; Weibel, Rikke; Whitehouse, Martin; Kristensen, Lars; Hjuler, Morten L.; Mathiesen, Anders; Boyce, Adrian J.; Nielsen, Lars H.

    2016-04-01

    Exploitation of geothermal sandstone reservoirs is challenged by pore-cementing minerals since they reduce the fluid flow through the sandstones. Geothermal exploration aims at finding sandstone bodies located at depths that are adequate for sufficiently warm water to be extracted, but without being too cemented for warm water production. The amount of cement is highly variable in the Danish geothermal reservoirs which mainly comprise the Bunter Sandstone, Skagerrak and Gassum formations. The present study involves bulk and in situ stable isotope analyses of calcite, dolomite, ankerite, siderite and quartz in order to estimate at what depth they were formed and enable prediction of where they can be found. The δ18O values measured in the carbonate minerals and quartz overgrowths are related to depth since they are a result of the temperatures of the pore fluid. Thus the values indicate the precipitation temperatures and they fit the relative diagenetic timing identified by petrographical observations. The sandstones deposited during arid climatic conditions contain calcite and dolomite cement that formed during early diagenesis. These carbonate minerals precipitated as a response to different processes, and precipitation of macro-quartz took over at deeper burial. Siderite was the first carbonate mineral that formed in the sandstones that were deposited in a humid climate. Calcite began precipitating at increased burial depth and ankerite formed during deep burial and replaced some of the other phases. Ankerite and quartz formed in the same temperature interval so constrains on the isotopic composition of the pore fluid can be achieved. Differences in δ13C values exist between the sandstones that were deposited in arid versus humid environments, which suggest that different kinds of processes were active. The estimated precipitation temperatures of the different cement types are used to predict which of them are present in geothermal sandstone reservoirs in

  17. Precipitation Reconstruction (PREC)

    Data.gov (United States)

    National Oceanic and Atmospheric Administration, Department of Commerce — The PREC data set is an analysis of monthly precipitation constructed on a 2.5(o)lat/lon grid over the global for the period from 1948 to the present. The land...

  18. Magnetic properties of Fe-Ni nanoparticles prepared by co-precipitation method

    Energy Technology Data Exchange (ETDEWEB)

    Davarpanah, A M; Sargazi, M [Department of Physics, University of Sistan and Baluchestan, Zahedan (Iran, Islamic Republic of); Mirzae, A A; Feizi, M [Department of Chemistry, University of Sistan and Baluchestan, Zahedan (Iran, Islamic Republic of)], E-mail: A.M.DAVARPANAH@hamoon.usb.ac.ir

    2008-08-15

    Many methods have been extended for the preparation of nanoparticles. One of the most important methods is the chemical wet process, e.g. the co-precipitation method that has been used for the preparation of Fe-Ni nanoparticles by the authors. XRD patterns show that the nanoparticles are amorphous before calcination and crystallized after calcination. SEM images show that the grain size of the Fe-Ni particles is in 50-300 nanometre range and that the texture of the nanoparticles after calcination was smoother than before calcination. Hysteresis loops show that the Fe-Ni nanoparticles are superparamagnetic before calcination, because the carbonate phase still exists in the sample, and that they are ferromagnetic materials after calcination. For 40Fe-60Ni nanoparticles after calcination, H{sub c} = 0.12 and B{sub s} = 4800 Oe, being very different in respect to the bulk 40Fe-60Ni alloy.

  19. Crystal Meth

    Science.gov (United States)

    ... for: Navigation Home / Stories of Hope / Crystal meth Crystal meth Story Of Hope By giovanni January 3rd, ... about my drug addiction having to deal with Crystal meth. I am now in recovery and fighting ...

  20. Amorphous iron (II) carbonate

    DEFF Research Database (Denmark)

    Sel, Ozlem; Radha, A.V.; Dideriksen, Knud;

    2012-01-01

    Abstract The synthesis, characterization and crystallization energetics of amorphous iron (II) carbonate (AFC) are reported. AFC may form as a precursor for siderite (FeCO3). The enthalpy of crystallization (DHcrys) of AFC is similar to that of amorphous magnesium carbonate (AMC) and more...

  1. Effect of carbon addition on carbide morphology of single crystal Ni-based superalloy%碳对镍基单晶高温合金碳化物形貌的影响

    Institute of Scientific and Technical Information of China (English)

    余竹焕; 刘林; 张军

    2014-01-01

    Single crystal superalloys of AM3 with different carbon levels were prepared at withdraw rate of 50μm/s. The effect of carbon addition on the carbide morphology was investigated. It was found that there were four types of MC-type carbides, acicular, nodular, blocky, and Chinese script-type in the crystals. With an increase in carbon level, the volume fraction of carbide increased significantly while the volume fraction of eutectic decreased significantly. Furthermore, the size of carbide in high level carbon alloy became much larger.%在抽拉速率为50μm/s的条件下制备5种不同含碳量的单晶高温合金,研究碳对单晶高温合金中碳化物形貌的影响。研究发现,铸态组织中存在4种形貌的MC型碳化物,呈针状、球状、块状以及中文汉字状。随着碳含量的增加,碳化物的体积分数增大而共晶组织的体积显著减少。同时,碳化物的尺寸随着碳含量的增加亦呈增大趋势。

  2. Radiation detection. Chapter 4. Effects of tellurium precipitates on charge collection in CZT (CdZnTe) nuclear radiation detectors

    International Nuclear Information System (INIS)

    It has been recently demonstrated that individual Tellurium (Te) precipitates identified with infrared (IR) transmission microscopes in radiation detector-grade CdZnTe (CZT) crystals correlate precisely with poor charge collection. This indicates that Te precipitates adversely affect the electron charge collection efficiency and thus the performance of nuclear radiation detectors produced from the crystals. By employing different techniques it is investigated how Te precipitates affect different CZT devices. These measurements indicate that Te precipitates put limits on the size, electrode configurations and spectral performance of CZT detectors. These limits can be relaxed by lowering the size and density of Te precipitates in the detectors

  3. Bench-Scale Development of a Hot Carbonate Absorption Process with Crystallization-Enabled High Pressure Stripping for Post-Combustion CO{sub 2} Capture

    Energy Technology Data Exchange (ETDEWEB)

    Lu, Yongqi

    2014-02-01

    This report summarizes the methodology and preliminary results of a techno-economic analysis on a hot carbonate absorption process (Hot-CAP) with crystallization-enabled high pressure stripping for post-combustion CO{sub 2} capture (PCC). This analysis was based on the Hot-CAP that is fully integrated with a sub-critical steam cycle, pulverized coal-fired power plant adopted in Case 10 of the DOE/NETL’s Cost and Performance Baseline for Fossil Energy Plants. The techno-economic analysis addressed several important aspects of the Hot-CAP for PCC application, including process design and simulation, equipment sizing, technical risk and mitigation strategy, performance evaluation, and cost analysis. Results show that the net power produced in the subcritical power plant equipped with Hot-CAP is 611 MWe, greater than that with Econoamine (550 MWe). The total capital cost for the Hot-CAP, including CO{sub 2} compression, is $399 million, less than that for the Econoamine PCC ($493 million). O&M costs for the power plant with Hot-CAP is $175 million annually, less than that with Econoamine ($178 million). The 20-year levelized cost of electricity (LCOE) for the power plant with Hot-CAP, including CO2 transportation and storage, is 119.4 mills/kWh, a 59% increase over that for the plant without CO2 capture. The LCOE increase caused by CO{sub 2} capture for the Hot-CAP is 31% lower than that for its Econoamine counterpart.

  4. Dissolution-precipitation reactions and permeability evolution from reactions of CO2-rich aqueous solutions with fractured basalt

    Science.gov (United States)

    Wells, R. K.; Xiong, W.; Bae, Y.; Sesti, E.; Skemer, P. A.; Giammar, D.; Conradi, M.; Ellis, B. R.; Hayes, S. E.

    2015-12-01

    The injection of CO2 into fractured basalts is one of several possible solutions to mitigate global climate change; however, research on carbonation in natural basalts in relation to carbon sequestration is limited, which impedes our understanding of the processes that may influence the viability of this strategy. We are conducting bench-scale experiments to characterize the mineral dissolution and precipitation and the evolution of permeability in synthetic and natural basalts exposed to CO2-rich fluids. Analytical methods include optical and electron microscopy, electron microprobe, Raman spectroscopy, nuclear magnetic resonance (NMR), and micro X-ray computed tomography (μCT) with variable flow rates. Reactive rock and mineral samples consist of 1) packed powders of olivine or natural basalt, and 2) sintered cores of olivine or a synthetic basalt mixture. Each sample was reacted in a batch reactor at 100 °C, and 100 bars CO2. Magnesite is detected within one day in olivine packed beds, and within 15 days in olivine sintered cores. Forsterite and synthetic basalt sinters were also reacted in an NMR apparatus at 102 °C and 65 bars CO2. Carbonate signatures are observed within 72 days of reaction. Longer reaction times are needed for carbonate precipitation in natural basalt samples. Cores from the Columbia River flood basalt flows that contain Mg-rich olivine and a serpentinized basalt from Colorado were cut lengthwise, the interface mechanically roughened or milled, and edges sealed with epoxy to simulate a fractured interface. The cores were reacted in a batch reactor at 50-150 °C and 100 bars CO2. At lower temperatures, calcite precipitation is rare within the fracture after 4 weeks. At higher temperatures, numerous calcite and aragonite crystals are observed within 1 mm of the fracture entrance along the roughened fracture surface. In flow-through experiments, permeability decreased along the fracture paths within a few hours to several days of flow.

  5. Quantification of asphaltene precipitation by scaling equation

    Science.gov (United States)

    Janier, Josefina Barnachea; Jalil, Mohamad Afzal B. Abd.; Samin, Mohamad Izhar B. Mohd; Karim, Samsul Ariffin B. A.

    2015-02-01

    Asphaltene precipitation from crude oil is one of the issues for the oil industry. The deposition of asphaltene occurs during production, transportation and separating process. The injection of carbon dioxide (CO2) during enhance oil recovery (EOR) is believed to contribute much to the precipitation of asphaltene. Precipitation can be affected by the changes in temperature and pressure on the crude oil however, reduction in pressure contribute much to the instability of asphaltene as compared to temperature. This paper discussed the quantification of precipitated asphaltene in crude oil at different high pressures and at constant temperature. The derived scaling equation was based on the reservoir condition with variation in the amount of carbon dioxide (CO2) mixed with Dulang a light crude oil sample used in the experiment towards the stability of asphaltene. A FluidEval PVT cell with Solid Detection System (SDS) was the instrument used to gain experimental knowledge on the behavior of fluid at reservoir conditions. Two conditions were followed in the conduct of the experiment. Firstly, a 45cc light crude oil was mixed with 18cc (40%) of CO2 and secondly, the same amount of crude oil sample was mixed with 27cc (60%) of CO2. Results showed that for a 45cc crude oil sample combined with 18cc (40%) of CO2 gas indicated a saturation pressure of 1498.37psi and asphaltene onset point was 1620psi. Then for the same amount of crude oil combined with 27cc (60%) of CO2, the saturation pressure was 2046.502psi and asphaltene onset point was 2230psi. The derivation of the scaling equation considered reservoir temperature, pressure, bubble point pressure, mole percent of the precipitant the injected gas CO2, and the gas molecular weight. The scaled equation resulted to a third order polynomial that can be used to quantify the amount of asphaltene in crude oil.

  6. Status of satellite precipitation retrievals

    Directory of Open Access Journals (Sweden)

    C. Kidd

    2011-04-01

    Full Text Available Satellites offer an unrivalled vantage point to observe and measure Earth system processes and parameters. Precipitation (rain and snow in particular, benefit from such observations since precipitation is spatially and temporally highly variable and with satellites overcoming some of the deficiencies of conventional gauge and radar measurements. This paper provides an overall review of quantitative precipitation estimation, covering the basis of the satellite systems used in the observation of precipitation, the dissemination and processing of this data, and the generation, availability and validation of these precipitation estimates. A selection of applications utilising these precipitation estimates are then outlined to exemplify the utility of such products.

  7. ANALYTICAL CHARACTERIZATION OF PRECIPITATIONS

    Directory of Open Access Journals (Sweden)

    Danut Tiberiu Epure

    2011-02-01

    Full Text Available The properties of precipitation are mainly determined by solid, liquid and gaseous substances that exist in suspended or dissolved form. These substances come from many complex interactions between the atmosphere – hydrosphere – lithosphere – biota. The analytical characterization of precipitation has been based on the analysis of several chemical parameters: pH, conductivity, chloride, fluoride and ammonium ions, total hardness, alkalinity, H2S and sulphides, COD (Mn, nitrites, phosphorous, metallic ions (total iron, copper and chromium. In this purpose were collected rainwater, ice and snow from different areas (cities Năvodari, Constanţa, Buzău and Mihail Kogălniceanu during November 2007 till February 2008. This study shows that chemical characteristics of the analyzed water samples vary from one region to another depending on the mineralogical composition of zones crossed, the contact time, temperature, weather conditions, the sampling period (day or night and the nature of sample (rain, snow, ice.

  8. Development of advanced reprocessing system based on precipitation method using pyrrolidone derivatives as precipitants. Overall evaluation of system

    International Nuclear Information System (INIS)

    An advanced reprocessing system for spent FBR fuels based on two precipitation processes using pyrrolidone derivatives as precipitants has been proposed. In order to develop this system, we have examined precipitation behavior of U(VI), Pu(IV), Pu(VI), and other metal cations with various pyrrolidone derivatives, the heat- and radiation-resistance of precipitants, the thermal decomposition properties of precipitates. As a result, it was found that N-n-butyl-2-pyrrolidone (NBP) and N-neopentyl-2-pyrrolidone (NNpP) are the appropriate precipitants for the first and second precipitation processes, respectively, that the decontamination factors for most of simulated fission products are more than 102, that the precipitant components are recovered by vaporization with heating the precipitates, and that the recovered precipitants are used repeatedly. Furthermore, we have performed the engineering investigation, and confirmed that the precipitation and the filtration can be done efficiently using the continuous precipitation apparatus and centrifugal separation machine, and that the pellets with density of 85- 90% TD and residual carbon less than 100 ppm are prepared by the calcination of the precipitates under wet-H2 at 1750degC. On the basis of results of basic and engineering investigations, we evaluated our proposed reprocessing system from the viewpoints of technical feasibility, safety, economical matter, effective use of U and Pu, reduction of radioactive wastes, nonproliferation, and so on. As a result, it was evaluated that our proposed system is expected to be one of candidates of the future reprocessing systems for spent FBR fuels. (author)

  9. Effect of humic substances on the precipitation of calcium phosphate

    Institute of Scientific and Technical Information of China (English)

    SONG Yong-hui; Hermann H. HAHN; Erhard HOFFMANN; Peter G. WEIDLER

    2006-01-01

    For phosphorus (P) recovery from wastewater, the effect of humic substances (HS) on the precipitation of calcium phosphate was studied. Batch experiments of calcium phosphate precipitation were undertaken with synthetic water that contained 20 mg/L phosphate (as P) and 20 mg/L HS (as dissolved organic carbon, DOC) at a constant pH value in the range of 8.0-10.0. The concentration variations of phosphate, calcium (Ca) and HS were measured in the precipitation process; the crystalline state and compositions of the precipitates were analysed by powder X-ray diffraction (XRD) and chemical methods, respectively. It showed that at solution pH 8.0, the precipitation rate and removal efficiency of phosphate were greatly reduced by HS, but at solution pH ≥9.0,the effect of HS was very small. The Ca consumption for the precipitation of phosphate increased when HS was added; HS was also removed from solution with the precipitation of calcium phosphate. At solution pH 8.0 and HS concentrations ≤ 3.5 mg/L, and at pH ≥ 9.0 and HS concentrations ≤ 10 mg/L, the final precipitates were proved to be hydroxyapatite (HAP) by XRD. The increases of solution pH value and initial Ca/P ratio helped reduce the influence of HS on the precipitation of phosphate.

  10. Is the contribution of bacteria to terrestrial carbon budget greatly underestimated?

    Science.gov (United States)

    Braissant, Olivier; Verrecchia, Eric; Aragno, Michel

    2002-07-01

    Some commonly found species of soil bacteria use low molecular weight organic acids as their sole source of carbon and energy. This study shows that acids such as citrate and oxalate (produced in large amounts by fungi and plants) can rapidly be consumed by these bacteria. Two strains, Ralstonia eutropha and Xanthobacter autotrophicus, were cultured on acetate- and citrate-rich media. The resulting CO2 and/or HCO3- reacted with calcium ions to precipitate two polymorphs of calcium carbonate (CaCO3), calcite and vaterite, depending on the quantity of slime produced by the strains. This production of primary calcium carbonate crystals by oxalate- and citrate-degrading bacteria from soil organic carbon sources highlights the existence of an important and underestimated potential carbon sink.

  11. Hourly Precipitation Data (HPD) Publication

    Data.gov (United States)

    National Oceanic and Atmospheric Administration, Department of Commerce — Hourly Precipitation Data (HPD) Publication is archived and available from the National Climatic Data Center (NCDC). This publication contains hourly precipitation...

  12. Modeling solid-state precipitation

    CERN Document Server

    Nebylov, AlexanderKozeschnik, Ernst

    2012-01-01

    Over recent decades, modeling and simulation of solid-state precipitation has attracted increased attention in academia and industry due to their important contributions in designing properties of advanced structural materials and in increasing productivity and decreasing costs for expensive alloying. In particular, precipitation of second phases is an important means for controlling the mechanical-technological properties of structural materials. However, profound physical modeling of precipitation is not a trivial task. This book introduces you to the classical methods of precipitation model

  13. Diffusion-driven precipitate growth and ripening of oxygen precipitates in boron doped silicon by dynamical x-ray diffraction

    Energy Technology Data Exchange (ETDEWEB)

    Will, J., E-mail: will@krist.uni-erlangen.de; Gröschel, A.; Bergmann, C.; Magerl, A. [Crystallography and Structural Physics, University of Erlangen-Nürnberg, Staudtstr. 3, 91058 Erlangen (Germany); Spiecker, E. [Center for Nanoanalysis and Electron Microscopy, University of Erlangen-Nürnberg, Cauerstr. 6, 91058 Erlangen (Germany)

    2014-03-28

    X-ray Pendellösung fringes from three silicon single crystals measured at 900 °C are analyzed with respect to density and size of oxygen precipitates within a diffusion-driven growth model and compared with TEM investigations. It appears that boron doped (p+) material shows a higher precipitate density and a higher strain than moderately (p-) boron crystals. In-situ diffraction reveals a diffusion-driven precipitate growth followed by a second growth regime in both materials. An interpretation of the second growth regime in terms of Ostwald ripening yields surface energy values (around 70 erg/cm{sup 2}) similar to published data. Further, an increased nucleation rate by a factor of ∼13 is found in the p+ sample as compared to a p- sample at a nucleation temperature of 450 °C.

  14. Precipitation Indices Low Countries

    Science.gov (United States)

    van Engelen, A. F. V.; Ynsen, F.; Buisman, J.; van der Schrier, G.

    2009-09-01

    Since 1995, KNMI published a series of books(1), presenting an annual reconstruction of weather and climate in the Low Countries, covering the period AD 763-present, or roughly, the last millennium. The reconstructions are based on the interpretation of documentary sources predominantly and comparison with other proxies and instrumental observations. The series also comprises a number of classifications. Amongst them annual classifications for winter and summer temperature and for winter and summer dryness-wetness. The classification of temperature have been reworked into peer reviewed (2) series (AD 1000-present) of seasonal temperatures and temperature indices, the so called LCT (Low Countries Temperature) series, now incorporated in the Millennium databases. Recently we started a study to convert the dryness-wetness classifications into a series of precipitation; the so called LCP (Low Countries Precipitation) series. A brief outline is given here of the applied methodology and preliminary results. The WMO definition for meteorological drought has been followed being that a period is called wet respectively dry when the amount of precipitation is considerable more respectively less than usual (normal). To gain a more quantitative insight for four locations, geographically spread over the Low Countries area (De Bilt, Vlissingen, Maastricht and Uccle), we analysed the statistics of daily precipitation series, covering the period 1900-present. This brought us to the following definition, valid for the Low Countries: A period is considered as (very) dry respectively (very) wet if over a continuous period of at least 60 days (~two months) cq 90 days (~three months) on at least two out of the four locations 50% less resp. 50% more than the normal amount for the location (based on the 1961-1990 normal period) has been measured. This results into the following classification into five drought classes hat could be applied to non instrumental observations: Very wet period

  15. Irradiation-induced precipitation modelling of ferritic steels

    Science.gov (United States)

    Yin, You Fa; Faulkner, Roy G.; Lu, Zheng

    2009-06-01

    In high strength low alloy (HSLA) steels typically used in reactor pressure vessels (RPV), irradiation-induced microstructure changes affect the performance of the components. One such change is precipitation hardening due to the formation of solute clusters and/or precipitates which form as a result of irradiation-enhanced solute diffusion and thermodynamic stability changes. The other is irradiation-enhanced tempering which is a result of carbide coarsening due to irradiation-enhanced carbon diffusion. Both effects have been studied using a recently developed Monte Carlo based precipitation kinetics simulation technique and modelling results are compared with experimental measurements. Good agreements have been achieved.

  16. Irradiation-induced precipitation modelling of ferritic steels

    Energy Technology Data Exchange (ETDEWEB)

    Yin, Y.F. [Department of Materials, Loughborough University, Ashby Road, Loughborough University, Leicestershire LE11 3TU (United Kingdom)], E-mail: y.yin@lboro.ac.uk; Faulkner, Roy G.; Zheng Lu [Department of Materials, Loughborough University, Ashby Road, Loughborough University, Leicestershire LE11 3TU (United Kingdom)

    2009-05-31

    In high strength low alloy (HSLA) steels typically used in reactor pressure vessels (RPV), irradiation-induced microstructure changes affect the performance of the components. One such change is precipitation hardening due to the formation of solute clusters and/or precipitates which form as a result of irradiation-enhanced solute diffusion and thermodynamic stability changes. The other is irradiation-enhanced tempering which is a result of carbide coarsening due to irradiation-enhanced carbon diffusion. Both effects have been studied using a recently developed Monte Carlo based precipitation kinetics simulation technique and modelling results are compared with experimental measurements. Good agreements have been achieved.

  17. Improving the analysis of small precipitates in HSLA steels using a plasma cleaner and ELNES.

    Science.gov (United States)

    Wilson, J A; Craven, A J

    2003-04-01

    The change from producing high strength low alloy (HSLA) steel sheet by conventional thick slab casting to producing it by direct charged thin slab casting causes a major change in the evolution of the precipitation. A key area of interest is the composition of the sub-10nm precipitates used to produce dispersion hardening. Carbon extraction replicas are frequently used to study precipitates in steels and other metals. When used with annular dark field imaging, this technique gives high contrast images of the precipitates while the thin carbon film adds little background or additional characteristic signals to either electron energy loss spectra or energy dispersive X-ray spectra. The method has the additional major advantage of removing the ferromagnetic matrix when studying HSLA steels. However, when the precipitates contain carbon, the C K-edge is dominated by the contribution from the amorphous carbon film. A plasma cleaner can be used to thin this carbon film to approximately 0.5 nm or less and then the contribution from the carbon in the precipitate can be separated from that in the carbon film using the electron energy loss near edge structure. A similar approach can be taken to separate the oxygen content of the precipitate from that of oxides formed from low-level impurities in the amorphous carbon during the plasma thinning process. In most cases, the precipitate studied here contained little or no oxygen even for the smallest sizes examined (approximately 4 nm). The precipitates contain mainly nitrogen with little carbon. For some compositions, the precipitates are clearly sub-stoichiometric. PMID:12524190

  18. Synthesis of hydrated lutetium carbonate

    Energy Technology Data Exchange (ETDEWEB)

    Song Liu [South China Univ. of Technology, Dept. of Applied Chemistry, Guangdong (China); Rong-jun Ma [Changsha Research Institute of Minig and Metallurgy, Hunan (China)

    1997-09-01

    Crystalline lutetium carbonate was synthesized for the corresponding chloride using ammonium bicarbonate as precipitant. The chemical analyses suggest that the synthesized lutetium carbonate is a hydrated basic carbonate or oxycarbonate. The X-ray powder diffraction data are presented. The IR data for the compound show the presence of two different carbonate groups. There is no stable intermediate carbonate in the process of thermal decomposition of the lutetium carbonate. (au) 15 refs.

  19. Particle size distribution dynamics during precipitative softening: constant solution composition.

    Science.gov (United States)

    Nason, Jeffrey A; Lawler, Desmond F

    2008-08-01

    In the treatment of surface water for potable use, precipitative coagulation (e.g., lime softening, alum or iron sweep coagulation) is widely utilized prior to particle removal processes. The particle size distribution (PSD) formed during such processes is a prime determinant of the removal efficiency for suspended and dissolved contaminants, but little is known quantitatively about how PSDs change by simultaneous precipitation and flocculation. Using precipitative softening as an example, detailed measurements of the PSD (using electronic particle counting) were made during precipitation of CaCO(3) under conditions of constant solution composition. Examination of the time-varying PSDs revealed dramatic changes resulting from nucleation, crystal growth, and flocculation. The influence of the saturation ratio, seed concentration, and mixing intensity on those processes was quantified. Implications with respect to the design and operation of water treatment facilities are discussed. PMID:18656223

  20. Influence des ions étrangers et de la matière organique sur la cristallisation des carbonates de calcium Influence of Foreign Ions and of Organic Matter on the Crystallization of Calcium Carbonates

    Directory of Open Access Journals (Sweden)

    Cailleau P.

    2006-11-01

    examines the influence of foreign ions and organic matter on the ger-mination and growth of calcium carbonates.The main results obtained can be summed up as follows:a Concerning Foreign Ions.Their action generally results in:- an increase in germination time and a reduction in the growth rate of CaC03 crystals:- the appearance of special facies for some of the minerals formed: - the inhibition of transformation from one variety ta another.A classification by order of increasing efficiency is obtained: - approximately zero action: K+, CI-;- moderate action: Bot+, Na+, A13+, Cul+, Sr 2+, S04-, P04- . - dominant action of Mg'+.b For Organic Matter.Citric acid and, ta a lesser extent, tartaric acid are the only ones ta have an appre ciable influence, moreover an influence which is similar to thot of foreign ions with regard ta kinetics of CaCO3 germination and growth.The adsorption of some of these products also results in special facies of the minerals formed and eventually in the inhibition of transformations from one variety ta another

  1. Effect of Impurities on Conversion of Gypsum and Crystallization of Calcium Carbonate%杂质对磷石膏与碳酸铵反应及产物碳酸钙结晶的影响

    Institute of Scientific and Technical Information of China (English)

    丁光月; 李岳; 樊彩梅; 荆宏健; 冯军强

    2011-01-01

    用碳酸铵与磷石膏反应制取硫酸铵是磷石膏利用的有效途径之一,但磷石膏中的杂质会对石膏的转化过程及碳酸钙的结晶产生不利影响,进而影响碳酸钙的分离过程.以二水硫酸钙与碳酸铵为原料,以磷酸、硝酸镁、氟化钠及酸不溶物(AI)为杂质添加剂,研究了磷石膏复分解反应制取硫酸铵过程中杂质P2O5、Mg2+、F-及AI对硫酸钙转化率的影响,并对反应产物碳酸钙的结晶形态和晶型进行了SEM和XRD分析.结果表明,杂质的存在不仅降低了石膏中硫的转化率,而且使碳酸钙的晶型和晶体形状发生了变化,从而将影响产物的物性和过滤性能.%An effective approach of phosphogypsum utilization is the production of ammonium sulfate from ammonium carbonate and phosphogypsum. However, impurities in phosphogypsum have a negative impact on gypsum transformation process and the crystallization of calcium carbonate , and thus on the separation process of calcium carbonate. In this paper, calcium sulfate dihydrate and ammonium carbonate were used as raw materials, with phosphoric acid, magnesium nitrate, sodium fluoride and acid-insoluble material(AI) as impurity additives, to investigate the effects of the impurities P, Mg2+ , F- and AI on the conversion of calcium sulfate. The crystal line state and morphology of the product calcium carbonate were characterized by SEM and XRD analysis. The results show that the impurities not only affected the conversion of sulfur in gypsum, but also changed the type and shape of calcium carbonate crystal, consequently, affected the physical properties and filtration performance of products.

  2. Ubiquitylation functions in the calcium carbonate biomineralization in the extracellular matrix.

    Directory of Open Access Journals (Sweden)

    Dong Fang

    Full Text Available Mollusks shell formation is mediated by matrix proteins and many of these proteins have been identified and characterized. However, the mechanisms of protein control remain unknown. Here, we report the ubiquitylation of matrix proteins in the prismatic layer of the pearl oyster, Pinctada fucata. The presence of ubiquitylated proteins in the prismatic layer of the shell was detected with a combination of western blot and immunogold assays. The coupled ubiquitins were separated and identified by Edman degradation and liquid chromatography/mass spectrometry (LC/MS. Antibody injection in vivo resulted in large amounts of calcium carbonate randomly accumulating on the surface of the nacreous layer. These ubiquitylated proteins could bind to specific faces of calcite and aragonite, which are the two main mineral components of the shell. In the in vitro calcium carbonate crystallization assay, they could reduce the rate of calcium carbonate precipitation and induce the calcite formation. Furthermore, when the attached ubiquitins were removed, the functions of the EDTA-soluble matrix of the prismatic layer were changed. Their potency to inhibit precipitation of calcium carbonate was decreased and their influence on the morphology of calcium carbonate crystals was changed. Taken together, ubiquitylation is involved in shell formation. Although the ubiquitylation is supposed to be involved in every aspect of biophysical processes, our work connected the biomineralization-related proteins and the ubiquitylation mechanism in the extracellular matrix for the first time. This would promote our understanding of the shell biomineralization and the ubiquitylation processes.

  3. Status of satellite precipitation retrievals

    Directory of Open Access Journals (Sweden)

    C. Kidd

    2010-10-01

    Full Text Available Satellites offer an unrivalled vantage point to observe and measure Earth system processes and parameters. Precipitation (rain and snow in particular, benefit from such observations since precipitation is spatially and temporally highly variable and overcomes some of the deficiencies of conventional gauge and radar measurements. This paper provides an overall review of quantitative precipitation estimation, covering the basis of the satellite systems used in the observation of precipitation and the dissemination of this data, the processing of these measurements to generate the rainfall estimates and the availability, verification and validation of these precipitation estimates.

  4. Carbonic anhydrase activators: X-ray crystal structure of the adduct of human isozyme II with L-histidine as a platform for the design of stronger activators.

    Science.gov (United States)

    Temperini, Claudia; Scozzafava, Andrea; Puccetti, Luca; Supuran, Claudiu T

    2005-12-01

    Activation of the carbonic anhydrase (CA, EC 4.2.1.1) isoforms hCA I, II, and IV with l-histidine and some of its derivatives has been investigated by kinetic and X-ray crystallographic methods. l-His was a potent activator of isozymes I and IV (activation constants in the range of 4-33microM), and a moderate hCA II activator (activation constant of 113microM). Both carboxy- as well as amino-substituted l-His derivatives, such as the methyl ester or the dipeptide carnosine (beta-Ala-His), acted as more efficient activators as compared to l-His. The X-ray crystallographic structure of the hCA II-l-His adduct showed the activator to be anchored at the entrance of the active site cavity, participating in an extended network of hydrogen bonds with the amino acid residues His64, Asn67, and Gln92 and, with three water molecules connecting it to the zinc-bound water. Although the binding site of l-His is similar to that of histamine, the first CA activator for which the X-ray crystal structure has been reported in complex with hCA II (Briganti, F.; Mangani, S.; Orioli, P.; Scozzafava, A.; Vernaglione, G.; Supuran, C. T. Biochemistry1997, 36, 10384) there are important differences of binding between the two structurally related activators, since histamine interacts among others with Asn67 and Gln92 (similarly to l-His), but also with Asn62 and not His64, whereas the number of water molecules connecting them to the zinc-bound water is different (two for histamine, three for l-His). Furthermore, the imidazole moieties of the two activators adopt different conformations when bound to the enzyme active site. Since neither the amino- nor carboxy moieties of l-His participate in interactions with amino acid moieties of the active site, they can be derivatized for obtaining more potent activators, with pharmacological applications for the enhancement of synaptic efficacy. This may constitute a novel approach for the treatment of Alzheimer's disease, aging, and other conditions in

  5. Preparation of ultrafine a-Al2O3 using precipitation-azeotropic distillation method

    Institute of Scientific and Technical Information of China (English)

    2008-01-01

    Ammonium aluminum carbonate hydroxide (AACH) was prepared by a precipitation-azeotropic distillation method,which uses aluminum sulfate as the Al source and ammonium carbonate as the precipitant.Then,AACH was calcined into ultrafine α-Al2O3 powder.The factors that influence the dispersion property of ultrafine α-Al2O3 powder are discussed in this paper,such as the methods of adding materials,surfactant,and drying methods.The changes of the structure and property of ultrafine alumina in the thermal treatment process are also studied.The morphological structure and properties of AACH are characterized by DTA/TGA,SEM,XRD,and ICP measurements.The results show that ultrafine α-Al2O3 powder with a uniform particle size and well-distributed property can be synthesized only after aluminum sulfate atomizes into ammonium carbonate,proper amount of PEG1000 is added as the dispersant,and the product is treated by azeotropic distillation.The phase transformation of alumina during the calcination process can be described as amorphous Al2O3→γ-Al2O3→θ-Al2O3→α-Al2O3.The crystal grain size and density of ultrafine alumina powder increase with the increase of the calcination temperature.After AACH has been calcined at 1200℃ for 2 h,the ultrafine α-Al2O3 with uniform particle size,spherical shape,and more than 99.97% purity is obtained and its powder is well dispersed.

  6. Differences in crystal habitus of natural and synthetic colloids

    Science.gov (United States)

    Wieczorek, Arkadiusz K.; Händel, Matthias; Totsche, Kai Uwe

    2014-05-01

    The formation of colloids from natural aqueous solutions is influenced by a multitude of biogeochemical and physicochemical processes and the presence of a large diversity of geogen and biogen, inorganic and organic solution phase components. A thereby frequently neglected class of components is the dissolved and colloidal phase organic matter (DOM). As DOM will interact with other solution phase components, we hypothesize that nanosized and colloidal particles formed in DOM bearing solutions may differ from synthetic precipitates either by size, shape, crystal habitus, crystallinity, composition or combinations of that. To investigate this, we analyzed natural colloidal particles collected from a limestone aquifer of the Upper Muschelkalk formation at Hainich National Park, Thuringia, Germany. Major groundwater components are Ca2+, Mg2+, Na+, SO42-, Cl-, HCO3- , and about 1 ppm of total organic carbon (TOC) in dissolved and colloidal form. Synthetic nanoparticles were precipitated from a series of oversaturated solutions containing single or mixtures of the following salts CaSO4, MgSO4, Ca(HCO3)2 NaCl typical for limestone environments. The solutions were produced with both natural groundwater and pure water (milli-Q). Droplets of such produced colloidal suspension were pipetted on silicon wafers and subject to air drying. The wafers were then analyzed by scanning electron microscopy (SEM) with energy-dispersive X-ray spectroscopy (EDX) and atomic force microscopy (AFM). We found that particles from oversaturated CaSO4 solution in pure water precipitate as large needle shaped crystals, whereas precipitates from CaSO4 solution in natural water were much smaller and showed a rosette like shape - similar in size and shape to gypsum crystals collected from the limestone formation water. Similar differences we found for other aqueous solution compositions. From this pilot study we presume that even minute amounts of dissolved and colloidal phase organic matter in

  7. Research on the Influence of Pyrolysis Reaction Rate on Light Magnesium Carbonate Crystal Morphology%热解反应速率对轻质碳酸镁晶体形貌影响研究

    Institute of Scientific and Technical Information of China (English)

    万建军; 于博; 刘安双

    2013-01-01

    针对重镁水热解反应特点,采用抽真空降低系统中CO2气体分压的方式,加速重镁水热解反应正向反应速率.通过观察、对比一定热解温度,不同真空度下反应生成的轻质碳酸镁晶体型貌,得出结论:降低CO2气体分压,提高热解反应速率,会减缓轻质碳酸镁晶体型貌由棒状→片状→球状这一转变过程.当热解温度为50℃,提高反应速率,会促进轻质碳酸镁晶体团聚,反应速率越快,团聚现象越明显.%According to the characteristics of the heavy magnesium water pyrolysis and using vacuum to reduce the partial pressure of C02 gas in the system, the positive reaction rate of the pyrolysis reaction of heavy magnesium water is accelerated. By observation and comparison of light magnesium carbonate crystal morphology generated with certain pyrolysis temperature and different degree of vacuum, it can be concluded that the transition process of the light magnesium carbonate crystal morphology will slow down when reducing the partial pressure of C02 gas and increasing the rate of pyrolysis reaction. When the temperature of pyrolysis reaches 50 ℃ , the reunion of light magnesium carbonate crystal will be accelerated by improving the reaction rate. The faster the reaction rate is, the more obvious the reunion phenomenon is.

  8. Responses of Carbon Cycling Key Processes to Precipitation Changes in Arid and Semiarid Grassland Ecosystems: A review%干旱半干旱地区草地碳循环关键过程对降雨变化的响应

    Institute of Scientific and Technical Information of China (English)

    彭琴; 齐玉春; 董云社; 何亚婷; 刘欣超; 孙良杰; 贾军强; 金钊

    2012-01-01

    未来全球气候变化背景下,全球或局部地区的降雨量及降雨时间分布将发生一定的变化。草地生态系统在全球碳收支中作用显著,对气候变化的反馈起着重要的作用。但由于草地多处于干旱半干旱地区,受到水分条件的限制,对降雨变化响应敏感,其碳源汇功能表现出很大的不确定性。为了更好地预测未来全球气候变化背景下草地的碳源汇功能及其对气候变化的进一步反馈,有必要深入研究决定草地碳源汇功能的两大碳循环关键过程——净初级生产力和土壤呼吸对降雨变化的响应特征及机制。本文对国内外有关草地生产力和土壤呼吸如何对降雨量、降雨强度、降雨频率和间隔时间进行响应的相关研究成果进行了综述,在此基础上指出了目前研究存在的不足,并对未来相关的重点研究方向进行了探讨和展望。%Climate models predict that the amounts and the timing of precipitation will change in the future,both globally and regionally.Given the sensitivity of grassland to water availability in arid and semiarid areas,the variability of precipitation will undoubtedly influence the net primary production(NPP) and soil respiration(Rs),the two most key processes of carbon cycles in these ecosystems.And then,it can change the carbon budget of grassland.Thus,in order to better predict the function of carbon budget of grassland in future precipitation scenario,it is crucial to investigate the responses of the two key processes(NPP and Rs) to precipitation changes in arid and semiarid grassland ecosystems.This paper reviews research progress at home and abroad on how NPP and Rs respond to precipitation changes,points out the areas for improvement and discusses about the topics where more focus is needed in the future:(1) Study of the effects of precipitations intensity,frequency and interval on the responses of NPP,especially below ground NPP;(2) By better

  9. in situ Calcite Precipitation for Contaminant Immobilization

    Energy Technology Data Exchange (ETDEWEB)

    Yoshiko Fujita; Robert W. Smith

    2009-08-01

    in situ Calcite Precipitation for Contaminant Immobilization Yoshiko Fujita (Yoshiko.fujita@inl.gov) (Idaho National Laboratory, Idaho Falls, Idaho, USA) Robert W. Smith (University of Idaho-Idaho Falls, Idaho Falls, Idaho, USA) Subsurface radionuclide and trace metal contaminants throughout the U.S. Department of Energy (DOE) complex pose one of DOE’s greatest challenges for long-term stewardship. One promising stabilization mechanism for divalent trace ions, such as the short-lived radionuclide strontium-90, is co-precipitation in calcite. Calcite, a common mineral in the arid western U.S., can form solid solutions with trace metals. The rate of trace metal incorporation is susceptible to manipulation using either abiotic or biotic means. We have previously demonstrated that increasing the calcite precipitation rate by stimulating the activity of urea hydrolyzing microorganisms can result in significantly enhanced Sr uptake. Urea hydrolysis causes the acceleration of calcium carbonate precipitation (and trace metal co-precipitation) by increasing pH and alkalinity, and also by liberating the reactive cations from the aquifer matrix via exchange reactions involving the ammonium ion derived from urea: H2NCONH2 + 3H2O ? 2NH4+ + HCO3- + OH- urea hydrolysis >X:2Ca + 2NH4+ ? 2>X:NH4 + Ca2+ ion exchange Ca2+ + HCO3- + OH- ? CaCO3(s) + H2O calcite precipitation where >X: is a cation exchange site on the aquifer matrix. This contaminant immobilization approach has several attractive features. Urea hydrolysis is catalyzed by the urease enzyme, which is produced by many indigenous subsurface microorganisms. Addition of foreign microbes is unnecessary. In turn the involvement of the native microbes and the consequent in situ generation of reactive components in the aqueous phase (e.g., carbonate and Ca or Sr) can allow dissemination of the reaction over a larger volume and/or farther away from an amendment injection point, as compared to direct addition of the reactants at

  10. Microstructure and Properties of M40 Carbon Fibre Reinforced Mg-Re-Zr Alloy Composites

    Institute of Scientific and Technical Information of China (English)

    Gaohui Wu; Meihui Song; Ziyang Xiu; Ning Wang; Wenshu Yang

    2009-01-01

    M40 carbon fibre reinforced rare earth magnesium alloy ZM6 composites with fibre volume fraction about 60%were fabricated by pressure infiltration method.The microstructure, interfacial morphology, and precipitation were studied by scanning electron microscopy, transmission electron microscopy, and energy dispersive Xray spectrometer.It was shown that the interfaces between Mg alloy and fibres were well bonded and free from cracks.The Mg12Nd phase was preferentially precipitated at the fibre/matrix interfaces, leading to the segregation of Nd at the interfaces and the dramatic decrease of Mg12Nd precipitation in the matrix far from interfaces.Crystal defects such as high-density dislocations and twins were observed in the matrix near the fibre/matrix interface.A high bending strength (1393 MPa) and elastic modulus (190 GPa) were achieved in M40/ZM6 composite.

  11. The Global Precipitation Climatology Project (GPCP) Combined Precipitation Dataset

    Science.gov (United States)

    Huffman, George J.; Adler, Robert F.; Arkin, Philip; Chang, Alfred; Ferraro, Ralph; Gruber, Arnold; Janowiak, John; McNab, Alan; Rudolf, Bruno; Schneider, Udo

    1997-01-01

    The Global Precipitation Climatology Project (GPCP) has released the GPCP Version 1 Combined Precipitation Data Set, a global, monthly precipitation dataset covering the period July 1987 through December 1995. The primary product in the dataset is a merged analysis incorporating precipitation estimates from low-orbit-satellite microwave data, geosynchronous-orbit -satellite infrared data, and rain gauge observations. The dataset also contains the individual input fields, a combination of the microwave and infrared satellite estimates, and error estimates for each field. The data are provided on 2.5 deg x 2.5 deg latitude-longitude global grids. Preliminary analyses show general agreement with prior studies of global precipitation and extends prior studies of El Nino-Southern Oscillation precipitation patterns. At the regional scale there are systematic differences with standard climatologies.

  12. Analysis of CZT crystals and detectors grown in Russia and the Ukraine by high-pressure Bridgman methods

    Energy Technology Data Exchange (ETDEWEB)

    H. Hermon; M. Schieber; R. B. James; E. Y. Lee; N. Yang; A. J. Antolak; D. H. Morse; C. Hackett; E. Tarver; N. N. P. Kolesnikov; Yu N. Ivanov; V. Komar; M. S. Goorsky; H. Yoon

    2000-01-10

    Sandia National Laboratories (SNL) is leading an effort to evaluate vertical high pressure Bridgman (VHPB) Cd{sub 1-x}Zn{sub x}Te (CZT) crystals grown in the former Soviet Union (FSU) (Ukraine and Russia), in order to study the parameters limiting the crystal quality and the radiation detector performance. The stoichiometry of the CZT crystals, with 0.04 < x < 0.25, has been determined by methods such as proton-induced X-ray emission (PIXE), X-ray diffraction (XRD), microprobe analysis and laser ablation ICP mass spectroscopy (LA-ICP/MS). Other methods such as triaxial double crystal x-ray diffraction (TADXRD), infrared transmission spectroscopy (IR), atomic force microscopy (AFM), thermoelectric emission spectroscopy (TEES) and laser induced transient charge technique (TCT) were also used to evaluate the material properties. The authors have measured the zinc distribution in a CZT ingot along the axial direction and also its homogeneity. The (Cd+Zn)/Te average ratio measured on the Ukraine crystals was 1.2, compared to the ratio of 0.9-1.06 on the Russian ingots. The IR transmission showed highly decorated grain boundaries with precipitates and hollow bubbles. Microprobe elemental analysis and LA-ICP/MS showed carbon precipitates in the CZT bulk and carbon deposits along grain boundaries. The higher concentration of impurities and the imperfect crystallinity lead to shorter electron and hole lifetimes in the range of 0.5--2 {micro}s and 0.1 {micro}s respectively, compared to 3--20 {micro}s and 1--7 {micro}s measured on US spectrometer grade CZT detectors. These results are consistent with the lower resistivity and worse crystalline perfection of these crystals, compared to US grown CZT. However, recently grown CZT from FSU exhibited better detector performance and good response to alpha particles.

  13. Measurement of solid precipitation with an optical disdrometer

    Directory of Open Access Journals (Sweden)

    A. Macke

    2007-04-01

    Full Text Available A study about measurements of solid precipitation using an optical disdrometer is presented. The optical disdrometer is an improved version of the ODM 470 disdrometer. It allows to measure hydrometeors within a size range of 0.4 to 22 mm in diameter. The main advantage of this instrument is its ability to estimate accurately precipitation even under strong wind conditions (Großklaus, 1996. To measure solid precipitation a geometrical model was developed to determine the mean cross-sectional area of snow crystals for different predefined shapes and sizes. It serves to develop an algorithm, which relates the mean cross sectional area of snow crystals to their maximum dimension, liquid water content, and terminal velocity. The algorithm was applied to disdrometer measurements during winter 1999/2000 in Uppsala/Sweden. Resulting precipitation was compared to independent measurements of a Geonor gauge and to manual measurements. In terms of daily precipitation the disdrometer shows a reliable performance.

  14. Precipitation extremes under climate change

    CERN Document Server

    O'Gorman, Paul A

    2015-01-01

    The response of precipitation extremes to climate change is considered using results from theory, modeling, and observations, with a focus on the physical factors that control the response. Observations and simulations with climate models show that precipitation extremes intensify in response to a warming climate. However, the sensitivity of precipitation extremes to warming remains uncertain when convection is important, and it may be higher in the tropics than the extratropics. Several physical contributions govern the response of precipitation extremes. The thermodynamic contribution is robust and well understood, but theoretical understanding of the microphysical and dynamical contributions is still being developed. Orographic precipitation extremes and snowfall extremes respond differently from other precipitation extremes and require particular attention. Outstanding research challenges include the influence of mesoscale convective organization, the dependence on the duration considered, and the need to...

  15. Characterization of CeO2-ZrO2 mixed oxides prepared by two different co-precipitation methods

    Institute of Scientific and Technical Information of China (English)

    YUE Mei; CUI Meisheng; ZHANG Na; LONG Zhiqi; HUANG Xiaowei

    2013-01-01

    A series of cerium zirconium mixed oxides were prepared by two co-precipitation methods using magnesium hydrogen carbonate (MHC) and mixed ammonia-ammonia hydrogen carbonate (AAHC) as precipitant respectively.The crystal structure,BET surface area and morphology of the produced cerium zirconium mixed oxides were characterized by X-ray diffraction (XRD),Brumauer-Emmett-Teller (BET) and scanning electron microscopy (SEM) techniques.The reduction-oxidation behavior and oxygen storage capacity (OSC) performance were also studied by temperature programmed reduction (TPR) and oxygen pulse chemical adsorption methods.The XRD results demonstrated that the cerium zirconium mixed oxides obtained by both methods possessed structure of cubic solid solution phase.The fresh surface area calcinated at 600 ℃,aged surface area after 1000 ℃ and OSC at 500 ℃ of cerium zirconium mixed oxides were determined to be 89.337,34.784 m2/g,and 567 μmol O2/g for MHC method and 122.010,46.307 m2/g,and 665 μmol O2/g for AAHC method,respectively.

  16. Simulation and Scale-up of Barium Sulphate Precipitation Process Using CFD Modeling

    Institute of Scientific and Technical Information of China (English)

    龚俊波; 卫宏远; 王静康; JohnGarsideb

    2005-01-01

    Some empirical mixing models were used to describe the imperfect mixing in precipitation process.However, the models can not, in general, reflect the details of interactions between mixing and crystallization in a vessel. In this study, CFD (computational fluid dynamics) technique were developed by simulating the precipitation of barium sulphate in stirred tanks by integration of population balance equations with a CFD solver. Two typical impellers, Rushton and pitched blade turbines, were employed for agitation. The influence of feed concentration and position on crystal product properties was investigated by CFD simulation. The scale-up of these precipitators was systematically studied. Significant effect on the crystal properties was found for the scale-up under some conditions.Keywords simulation, scale up, precipitation, CFD(computational fluid dynamics)

  17. Microbially mediated mineral carbonation

    Science.gov (United States)

    Power, I. M.; Wilson, S. A.; Dipple, G. M.; Southam, G.

    2010-12-01

    Mineral carbonation involves silicate dissolution and carbonate precipitation, which are both natural processes that microorganisms are able to mediate in near surface environments (Ferris et al., 1994; Eq. 1). (Ca,Mg)SiO3 + 2H2CO3 + H2O → (Ca,Mg)CO3 + H2O + H4SiO4 + O2 (1) Cyanobacteria are photoautotrophs with cell surface characteristics and metabolic processes involving inorganic carbon that can induce carbonate precipitation. This occurs partly by concentrating cations within their net-negative cell envelope and through the alkalinization of their microenvironment (Thompson & Ferris, 1990). Regions with mafic and ultramafic bedrock, such as near Atlin, British Columbia, Canada, represent the best potential sources of feedstocks for mineral carbonation. The hydromagnesite playas near Atlin are a natural biogeochemical model for the carbonation of magnesium silicate minerals (Power et al., 2009). Field-based studies at Atlin and corroborating laboratory experiments demonstrate the ability of a microbial consortium dominated by filamentous cyanobacteria to induce the precipitation of carbonate minerals. Phototrophic microbes, such as cyanobacteria, have been proposed as a means for producing biodiesel and other value added products because of their efficiency as solar collectors and low requirement for valuable, cultivable land in comparison to crops (Dismukes et al., 2008). Carbonate precipitation and biomass production could be facilitated using specifically designed ponds to collect waters rich in dissolved cations (e.g., Mg2+ and Ca2+), which would allow for evapoconcentration and provide an appropriate environment for growth of cyanobacteria. Microbially mediated carbonate precipitation does not require large quantities of energy or chemicals needed for industrial systems that have been proposed for rapid carbon capture and storage via mineral carbonation (e.g., Lackner et al., 1995). Therefore, this biogeochemical approach may represent a readily

  18. Status of satellite precipitation retrievals

    OpenAIRE

    Kidd, C.; V. Levizzani

    2010-01-01

    Satellites offer an unrivalled vantage point to observe and measure Earth system processes and parameters. Precipitation (rain and snow) in particular, benefit from such observations since precipitation is spatially and temporally highly variable and overcomes some of the deficiencies of conventional gauge and radar measurements. This paper provides an overall review of quantitative precipitation estimation, covering the basis of the satellite systems used in the observation of precipi...

  19. Kinetics of barium sulphate reaction crystallization in crystallizers with internal circulation

    OpenAIRE

    Koralewska, J.; Piotrowski, K; B. Wierzbowska; A. Matynia

    2008-01-01

    Kinetic calculation results describing the observed nucleation and growth rates of barium sulphate crystals precipitated in an integrated reaction-crystallization process in a barium sulphate-ammonium chloride-water system are presented and analyzed. The scope of experiments included two continuous model DTM-type crystallizers (Draft Tube Magma) with internal circulation of the suspension forced by a liquid jet-pump device responsible for stable and intensive enough ascending/descending flow ...

  20. Effective Assimilation of Global Precipitation

    Science.gov (United States)

    Lien, G.; Kalnay, E.; Miyoshi, T.; Huffman, G. J.

    2012-12-01

    Assimilating precipitation observations by modifying the moisture and sometimes temperature profiles has been shown successful in forcing the model precipitation to be close to the observed precipitation, but only while the assimilation is taking place. After the forecast start, the model tends to "forget" the assimilation changes and lose their extra skill after few forecast hours. This suggests that this approach is not an efficient way to modify the potential vorticity field, since this is the variable that the model would remember. In this study, the ensemble Kalman filter (EnKF) method is used to effectively change the potential vorticity field by allowing ensemble members with better precipitation to receive higher weights. In addition to using an EnKF, two other changes in the precipitation assimilation process are proposed to solve the problems related to the highly non-Gaussian nature of the precipitation variable: a) transform precipitation into a Gaussian distribution based on its climatological distribution, and b) only assimilate precipitation at the location where some ensemble members have positive precipitation. The idea is first tested by the observing system simulation experiments (OSSEs) using SPEEDY, a simplified but realistic general circulation model. When the global precipitation is assimilated in addition to conventional rawinsonde observations, both the analyses and the medium range forecasts are significantly improved as compared to only having rawinsonde observations. The improvement is much reduced when only modifying the moisture field with the same approach, which shows the importance of the error covariance between precipitation and all other model variables. The effect of precipitation assimilation is larger in the Southern Hemisphere than that in the Northern Hemisphere because the Northern Hemisphere analyses are already accurate as a result of denser rawinsonde stations. Assimilation of precipitation using a more comprehensive