Aspen HYSYS process simulation and Aspen ICARUS cost estimation of CO2 removal plant

OpenAIRE

Vozniuk, Ievgeniia Oleksandrivna

2010-01-01

An Aspen HYSYS model of CO2 removal was developed and modified with a split-stream configuration in order to reduce energy consumption in the reboiler. The model has been calculated with variation of parameters to optimize the process and find an optimum solution. For the selected base cases the heat exchanger minimum temperature difference was specified to 10K and the removal efficiency was 85%. The reboiler duty of 3.8 MJ/kg CO2 removed for the standard process without split-stream was ...

Concurrent CO2 Control and O2 Generation for Advanced Life Support

Science.gov (United States)

Paul, Heather L.; Duncan, Keith L.; Hagelin-Weaver, Helena E.; Bishop, Sean R.; Wachsman, Eric D.

2007-01-01

The electrochemical reduction of carbon dioxide (CO2) using ceramic oxygen generators (COGs) is well known and widely studied, however, conventional devices using yttria-stabilized zirconia (YSZ) electrolytes operate at temperatures greater than 700 C. Operating at such high temperatures increases system mass compared to lower temperature systems because of increased energy overhead to get the COG up to operating temperature and the need for heavier insulation and/or heat exchangers to reduce the COG oxygen (O2) output temperature for comfortable inhalation. Recently, the University of Florida developed novel ceramic oxygen generators employing a bilayer electrolyte of gadolinia-doped ceria and erbia-stabilized bismuth for NASA's future exploration of Mars. To reduce landed mass and operation expenditures during the mission, in-situ resource utilization was proposed using these COGs to obtain both lifesupporting oxygen and oxidant/propellant fuel, by converting CO2 from the Mars atmosphere. The results showed that oxygen could be reliably produced from CO2 at temperatures as low as 400 C. These results indicate that this technology could be adapted to CO2 removal from a spacesuit and other applications in which CO2 removal was an issue. The strategy proposed for CO2 removal for advanced life support systems employs a catalytic layer combined with a COG so that it is reduced all the way to solid carbon and oxygen. Hence, a three-phased approach was used for the development of a viable low weight COG for CO2 removal. First, to reduce the COG operating temperature a high oxide ion conductivity electrolyte was developed. Second, to promote full CO2 reduction while avoiding the problem of carbon deposition on the COG cathode, novel cathodes and a removable catalytic carbon deposition layer were designed. Third, to improve efficiency, a pre-stage for CO2 absorption was used to concentrate CO2 from the exhalate before sending it to the COG. These subsystems were then

Adsorption removal of carbon dioxide from the helium coolant of high-temperature gas-cooled reactors

International Nuclear Information System (INIS)

Varezhin, A.V.; Fedoseenkov, A.N.; Khrulev, A.A.; Metlik, I.V.; Zel venskii, Y.D.

1986-01-01

This paper conducts experiments on the removal of CO 2 from helium by means of a Soviet-made adsorbent under the conditions characteristic of high-temperature gas-cooled reactor cleaning systems. The adsorption of CO 2 from helium was studied under dynamic conditions with a fixed layer of adsorbent in a flow-through apparatus with an adsorber 16 mm in diameter. The analysis of the helium was carried out by means of a TVT chromatograph. In order to compare the adsorption of CO 2 on CaA zeolite under dynamic conditions from the helium stream under pressure with the equilibrium adsorption on the basis of pure CO 2 , the authors determined the adsorption isotherm at 293 K by the volumetric method over a range of CO 2 equilibrium pressures from 260 to 11,970 Pa. Reducing the adsorption temperature to 273 K leads to a considerable reduction in the energy costs for regeneration, owing to the increase in adsorption and the decrease in the number of regeneration cycles; the amount of the heating gas used is reduced to less than half

Investigational study of the CO2 balance in high temperature CO2 separation technology; Nisanka tanso koon bunri gijutsu ni okeru CO2 balance ni kansuru chosa kenkyu

Energy Technology Data Exchange (ETDEWEB)

NONE

1997-03-01

An investigational study was conducted to clarify the adaptable environment and effectivity of technologies of high temperature separation/recovery/reutilization of CO2. In the study, data collection, arrangement and comparison were made of various separation technologies such as the membrane method, absorption method, adsorption method, and cryogenic separation method. With the LNG-fired power generation as an example, the adaptable environment and effectivity were made clear by making models by a process simulator, ASPEN PLUS. Moreover, using this simulator, effects of replacing the conventional steam reforming of hydrocarbon with the CO2 reforming were made clear with the methanol synthesis as an example. As to the rock fixation treatment of high temperature CO2, collection/arrangement were made of the data on the fixation treatment of the CO2 separated at high temperature into basic rocks such as peridotite and serpentinite in order to clarify the adaptable environment and effectivity of the treatment. Besides, a potentiality of the fixation to concrete waste was made clear. 57 refs., 57 figs., 93 tabs.

High-temperature radiation-induced removal of gaseous air pollutants

International Nuclear Information System (INIS)

Medina Rojas, I.; Thomson, M.J.

2001-01-01

This paper explores the use of high-temperature electron beam irradiation to simultaneous remove aromatic hydrocarbons, chlorinated hydrocarbons and nitrogen oxides. Detailed chemical kinetic modeling with validated mechanisms predicts that electron beam irradiation will simultaneously reduce NO with the thermal De-NO x process and oxidize benzene or ethyl chloride over a wide temperature range. Electron beam dosage of 2-10 kGy more than double the width of the temperature window over which the thermal De-NO x process is effective. At these dosages, the benzene and ethyl chloride removal efficiencies can exceed 90% within this temperature window. (author)

VUV-absorption cross section of CO2 at high temperatures and impact on exoplanet atmospheres

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Venot Olivia

2014-02-01

Full Text Available Ultraviolet (UV absorption cross sections are an essential ingredient of photochemical atmosphere models. Exoplanet searches have unveiled a large population of short-period objects with hot atmospheres, very different from what we find in our solar system. Transiting exoplanets whose atmospheres can now be studied by transit spectroscopy receive extremely strong UV fluxes and have typical temperatures ranging from 400 to 2500 K. At these temperatures, UV photolysis cross section data are severely lacking. Our goal is to provide high-temperature absorption cross sections and their temperature dependency for important atmospheric compounds. This study is dedicated to CO2, which is observed and photodissociated in exoplanet atmospheres. We performed these measurements for the 115 - 200 nm range at 300, 410, 480, and 550 K. In the 195 - 230 nm range, we worked at seven temperatures between 465 and 800 K. We found that the absorption cross section of CO2 is very sensitive to temperature, especially above 160 nm. Within the studied range of temperature, the CO2 cross section can vary by more than two orders of magnitude. This, in particular, makes the absorption of CO2 significant up to wavelengths as high as 230 nm, while it is negligible above 200 nm at 300 K. To investigate the influence of these new data on the photochemistry of exoplanets, we implemented the measured cross section into a 1D photochemical model. The model predicts that accounting for this temperature dependency of CO2 cross section can affect the computed abundances of NH3, CO2, and CO by one order of magnitude in the atmospheres of hot Jupiter and hot Neptune.

[Steam and air co-injection in removing TCE in 2D-sand box].

Science.gov (United States)

Wang, Ning; Peng, Sheng; Chen, Jia-Jun

2014-07-01

Steam and air co-injection is a newly developed and promising soil remediation technique for non-aqueous phase liquids (NAPLs) in vadose zone. In this study, in order to investigate the mechanism of the remediation process, trichloroethylene (TCE) removal using steam and air co-injection was carried out in a 2-dimensional sandbox with different layered sand structures. The results showed that co-injection perfectly improved the "tailing" effect compared to soil vapor extraction (SVE), and the remediation process of steam and air co-injection could be divided into SVE stage, steam strengthening stage and heat penetration stage. Removal ratio of the experiment with scattered contaminant area was higher and removal speed was faster. The removal ratios from the two experiments were 93.5% and 88.2%, and the removal periods were 83.9 min and 90.6 min, respectively. Steam strengthened the heat penetration stage. The temperature transition region was wider in the scattered NAPLs distribution experiment, which reduced the accumulation of TCE. Slight downward movement of TCE was observed in the experiment with TCE initially distributed in a fine sand zone. And such downward movement of TCE reduced the TCE removal ratio.

Coral energy reserves and calcification in a high-CO2 world at two temperatures.

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Verena Schoepf

Full Text Available Rising atmospheric CO2 concentrations threaten coral reefs globally by causing ocean acidification (OA and warming. Yet, the combined effects of elevated pCO2 and temperature on coral physiology and resilience remain poorly understood. While coral calcification and energy reserves are important health indicators, no studies to date have measured energy reserve pools (i.e., lipid, protein, and carbohydrate together with calcification under OA conditions under different temperature scenarios. Four coral species, Acropora millepora, Montipora monasteriata, Pocillopora damicornis, Turbinaria reniformis, were reared under a total of six conditions for 3.5 weeks, representing three pCO2 levels (382, 607, 741 µatm, and two temperature regimes (26.5, 29.0 °C within each pCO2 level. After one month under experimental conditions, only A. millepora decreased calcification (-53% in response to seawater pCO2 expected by the end of this century, whereas the other three species maintained calcification rates even when both pCO2 and temperature were elevated. Coral energy reserves showed mixed responses to elevated pCO2 and temperature, and were either unaffected or displayed nonlinear responses with both the lowest and highest concentrations often observed at the mid-pCO2 level of 607 µatm. Biweekly feeding may have helped corals maintain calcification rates and energy reserves under these conditions. Temperature often modulated the response of many aspects of coral physiology to OA, and both mitigated and worsened pCO2 effects. This demonstrates for the first time that coral energy reserves are generally not metabolized to sustain calcification under OA, which has important implications for coral health and bleaching resilience in a high-CO2 world. Overall, these findings suggest that some corals could be more resistant to simultaneously warming and acidifying oceans than previously expected.

High-resolution transmission measurements of CO2 at high temperatures for industrial applications

DEFF Research Database (Denmark)

Evseev, Vadim; Fateev, Alexander; Clausen, Sønnik

2012-01-01

. The spectra have been recorded in a high-temperature flow gas cell and using a Fourier transform infrared (FTIR) spectrometer at a nominal resolution of 0.125 cm-1. The volume fractions of CO2 in the measurements were 1,10 and 100%. The measurements have been validated by comparison with medium...

CO{sub 2} as an Oxidant for High-Temperature Reactions

Energy Technology Data Exchange (ETDEWEB)

Kawi, Sibudjing, E-mail: chekawis@nus.edu.sg; Kathiraser, Yasotha [Department of Chemical and Biomolecular Engineering, Faculty of Engineering, National University of Singapore, Singapore (Singapore)

2015-03-18

This paper presents a review on the developments in catalyst technology for the reactions utilizing CO{sub 2} for high-temperature applications. These include dehydrogenation of alkanes to olefins, the dehydrogenation of ethylbenzene to styrene, and finally CO{sub 2} reforming of hydrocarbon feedstock (i.e., methane) and alcohols. Aspects on the various reaction pathways are also highlighted. The literature on the role of promoters and catalyst development is critically evaluated. Most of the reactions discussed in this review are exploited in industries and related to on-going processes, thus providing extensive data from literature. However, some reactions, such as CO{sub 2} reforming of ethanol and glycerol, which have not reached industrial scale, are also reviewed owing to their great potential in terms of sustainability, which is essential as energy for the future. This review further illustrates the building-up of knowledge that shows the role of support and catalysts for each reaction and the underlying linkage between certain catalysts, which can be adapted for the multiple CO{sub 2}-related reactions.

High temperature CO2 capture using calcium oxide sorbent in a fixed-bed reactor

International Nuclear Information System (INIS)

Dou Binlin; Song Yongchen; Liu Yingguang; Feng Cong

2010-01-01

The gas-solid reaction and breakthrough curve of CO 2 capture using calcium oxide sorbent at high temperature in a fixed-bed reactor are of great importance, and being influenced by a number of factors makes the characterization and prediction of these a difficult problem. In this study, the operating parameters on reaction between solid sorbent and CO 2 gas at high temperature were investigated. The results of the breakthrough curves showed that calcium oxide sorbent in the fixed-bed reactor was capable of reducing the CO 2 level to near zero level with the steam of 10 vol%, and the sorbent in CaO mixed with MgO of 40 wt% had extremely low capacity for CO 2 capture at 550 deg. C. Calcium oxide sorbent after reaction can be easily regenerated at 900 deg. C by pure N 2 flow. The experimental data were analyzed by shrinking core model, and the results showed reaction rates of both fresh and regeneration sorbents with CO 2 were controlled by a combination of the surface chemical reaction and diffusion of product layer.

In-operando elucidation of bimetallic CoNi nanoparticles during high-temperature CH 4 /CO 2 reaction

KAUST Repository

Al-Sabban, Bedour E.; Falivene, Laura; Kozlov, Sergey M.; Aguilar Tapia, Antonio; Ould-Chikh, Samy; Hazemann, Jean-Louis; Cavallo, Luigi; Basset, Jean-Marie; Takanabe, Kazuhiro

2017-01-01

Dry reforming of methane (DRM) proceeds via CH4 decomposition to leave surface carbon species, followed by their removal with CO2-derived species. Reactivity tuning for stoichiometric CH4/CO2 reactants was attempted by alloying the non-noble metals

Removal of Hg, As in FGD gypsum by different aqueous ammonia (amines) during CO2 sequestration.

Science.gov (United States)

Wenyi, Tan; Wenhui, Fan; Hongyi, Li; Zixin, Zhang; Yunkun, Zhu

2017-12-01

CO 2 sequestration by flue gas desulfurization gypsum (FGDG) has become a promising FGDG disposal technology due to simultaneous CO 2 emission reduction and FGDG conversion into calcium carbonate. In this paper, another merit of the novel technology, i.e., the removal of toxic elements (e.g., Hg and As) in FGDG, will be addressed for the first time. In three different aqueous ammonia (or amines) media, removal efficiencies of Hg and As in FGDG samples were evaluated during CO 2 sequestration. Higher than 90% and 20% removal efficiencies, respectively, for Hg and As are achieved at 40°C in aqueous ammonia media, but they decrease at elevated temperatures. Ammonia loss takes place at 80°C and pH varies greatly with temperatures in aqueous ammonia. This is disadvantageous for the formation of Hg-ammonia complexes and for the yield of carbonates, which are responsible for Hg or As re-adsorption. The sequential chemical extraction method suggests that the speciation changes of Hg are induced by FGDG carbonation, and that unstable Hg speciation in triethanolamine increases at elevated temperatures.

Hydrogen purification by selective methanation of CO in CO/CO2/H2

DEFF Research Database (Denmark)

Andersen, Anne Mette; Johannessen, Tue; Livbjerg, Hans

down through the reactor and inside the catalyst pellets/particles. The small particles, which have a rather high effectiveness factor with respect to methanation of CO, have a high CO selectivity, whereas the larger pellets have very low selectivity even at high CO inlet concentrations. Negative...... of reaction kinetics and pore diffusion is crucial for interpreting the experimental data. We have found that the selectivity decreases by increasing the reactor temperature or catalyst particle size and when the CO inlet concentration is reduced. As a result, the selectivity drops significantly...... in an integral reactor operating at high CO-conversion. The lower limit of CO concentration in the outlet is determined by the quasi-equilibrium between CO removal and CO production from CO2....

Method of preparation of a CO.sub.2 removal sorbent with high chemical stability during multiple cycles

Science.gov (United States)

Siriwardane, Ranjani V.; Rosencwaig, Shira

2015-07-14

Method for the production of a clay-alkali-amine CO.sub.2 sorbent prepared by integrating a clay substrate, basic alkali salt, and amine liquid. The basic alkali salt is present relative to the clay substrate in a weight ratio of from about 1 part to about 50 parts per 100 parts of the clay substrate. The amine liquid is present relative to a clay-alkali combination in a weight ratio of from about 1 part to about 10 parts per 10 parts of the clay-alkali combination. The clay substrate and basic alkali salt may be combined in a solid-solid heterogeneous mixture and followed by introduction of the amine liquid. Alternatively, an alkaline solution may be blended with the amine solution prior to contacting the clay substrate. The clay-alkali-amine CO.sub.2 sorbent is particularly advantageous for low temperature CO.sub.2 removal cycles in a gas stream having a CO.sub.2 concentration less than around 2000 ppm and an oxygen concentration around 21%, such as air. Results are presented illustrating the performance of the clay-alkali-amine CO.sub.2 sorbent compared to a clay-amine sorbent lacking the alkali inclusion.

Investigation of H2S and CO2 Removal from Gas Streams Using Hollow Fiber Membrane Gas–liquid Contactors

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S. M. Mirfendereski

2017-07-01

Full Text Available Chemical absorption of H2S and CO2 from CH4 was carried out in a polypropylene porous asymmetric hollow fiber membrane contactor (HFMC. A 0.5 mol L–1 aqueous solution of methyldiethanolamine (MDEA was used as chemical absorbent solution. Effects of gas flow rate, liquid flow rate, H2S concentration and CO2 concentration on the H2S outlet concentrations and CO2 removal percentage were investigated. The results showed that the removal of H2S with aqueous solution of MDEA was very high and indicated almost total removal of H2S. Experimental results also indicated that the membrane contactor was very efficient in the removal of trace H2S at high gas/ liquid flow ratio. The removal of H2S was almost complete with a recovery of more than 96 %. Using feed gas mixtures containing 5000 ppm H2S with CO2 concentrations in the range of 4–12 vol.%, the outlet H2S concentration of less than 1.0 ppm was attained with less than 4.0 vol.% of CO2 permeated and absorbed.

An Innovative Configuration for CO2 Capture by High Temperature Fuel Cells

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Federico Rossi

2014-09-01

Full Text Available Many technological solutions have been proposed for CO2 capture in the last few years. Most of them are characterized by high costs in terms of energy consumption and, consequently, higher fossil fuel use and higher economic costs. High temperature fuel cells are technological solutions currently developed for energy production with low environmental impact. In CIRIAF—University of Perugia labs, cylindrical geometry, small-sized molten carbonate fuel cell (MCFC prototypes were built and tested with good energy production and lifetime performances. In the present work, an innovative application for MCFCs is proposed, and an innovative configuration for CO2 capture/separation is investigated. The plant scheme is based on a reformer and a cylindrical MCFC. MCFCs are the most suitable solutions, because CO2 is used in their operating cycle. An analysis in terms of energy consumption/kgCO2 captured is made by coupling the proposed configuration with a gas turbine plant. The proposed configuration is characterized by a theoretical energy consumption of about 500 kJ/kgCO2, which is quite lower than actual sequestration technologies. An experimental campaign will be scheduled to verify the theoretical findings.

Mixed Wastewater Coupled with CO2 for Microalgae Culturing and Nutrient Removal.

Directory of Open Access Journals (Sweden)

Lili Yao

Full Text Available Biomass, nutrient removal capacity, lipid productivity and morphological changes of Chlorella sorokiniana and Desmodesmus communis were investigated in mixed wastewaters with different CO2 concentrations. Under optimal condition, which was 1:3 ratio of swine wastewater to second treated municipal wastewater with 5% CO2, the maximum biomass concentrations were 1.22 g L-1 and 0.84 g L-1 for C. sorokiniana and D. communis, respectively. Almost all of the ammonia and phosphorus were removed, the removal rates of total nitrogen were 88.05% for C. sorokiniana and 83.18% for D. communis. Lipid content reached 17.04% for C. sorokiniana and 20.37% for D. communis after 10 days culture. CO2 aeration increased intracellular particle numbers of both microalgae and made D. communis tend to be solitary. The research suggested the aeration of CO2 improve the tolerance of microalgae to high concentration of NH4-N, and nutrient excess stress could induce lipid accumulation of microalgae.

Stem juice production of the C4 sugarcane (Saccharum officinarum) is enhanced by growth at double-ambient CO2 and high temperature.

Science.gov (United States)

Vu, Joseph C V; Allen, Leon H

2009-07-15

Two cultivars of sugarcane (Saccharum officinarum cv. CP73-1547 and CP88-1508) were grown for 3 months in paired-companion, temperature-gradient, sunlit greenhouses under daytime [CO2] of 360 (ambient) and 720 (double ambient) micromol mol(-1) and at temperatures of 1.5 degrees C (near ambient) and 6.0 degrees C higher than outside ambient temperature. Leaf area and biomass, stem biomass and juice and CO2 exchange rate (CER) and activities of ribulose bisphosphate carboxylase-oxygenase (Rubisco) and phosphoenolpyruvate carboxylase (PEPC) of fully developed leaves were measured at harvest. On a main stem basis, leaf area, leaf dry weight, stem dry weight and stem juice volume were increased by growth at doubled [CO2] or high temperature. Such increases were even greater under combination of doubled [CO2]/high temperature. Plants grown at doubled [CO2]/high temperature combination averaged 50%, 26%, 84% and 124% greater in leaf area, leaf dry weight, stem dry weight and stem juice volume, respectively, compared with plants grown at ambient [CO2]/near-ambient temperature combination. In addition, plants grown at doubled [CO2]/high temperature combination were 2-3-fold higher in stem soluble solids than those at ambient [CO2]/near-ambient temperature combination. Although midday CER of fully developed leaves was not affected by doubled [CO2] or high temperature, plants grown at doubled [CO2] were 41-43% less in leaf stomatal conductance and 69-79% greater in leaf water-use efficiency, compared with plants grown at ambient [CO2]. Activity of PEPC was down-regulated 23-32% at doubled [CO2], while high temperature did not have a significant impact on this enzyme. Activity of Rubisco was not affected by growth at doubled [CO2], but was reduced 15-28% at high temperature. The increases in stem juice production and stem juice soluble solids concentration for sugarcane grown at doubled [CO2] or high temperature, or at doubled [CO2]/high temperature combination, were partially

Combined CO/CH4 oxidation tests over Pd/Co3O4 monolithic catalyst. Effects of high reaction temperature and SO2 exposure on the deactivation process

International Nuclear Information System (INIS)

Liotta, L.F.; Venezia, A.M.; Di Carlo, G.; Pantaleo, G.; Deganello, G.; Merlone Borla, E.; Pidria, M.

2007-01-01

CO and CH 4 combined oxidation tests were performed over a Pd (70 g/ft 3 )/Co 3 O 4 monolithic catalyst in conditions of GHSV = 100,000 h -1 and feed composition close to that of emission from bi-fuel vehicles. The effect of SO 2 (5 ppm) on CO and CH 4 oxidation activity under lean condition (λ 2) was investigated. The presence of sulphur strongly deactivated the catalyst towards methane oxidation, while the poisoning effect was less drastic in the oxidation of CO. Saturation of the Pd/Co 3 O 4 catalytic sites via chemisorbed SO 3 and/or sulphates occurred upon exposure to SO 2 . A treatment of regeneration to remove sulphate species was attempted by performing a heating/cooling cycle up to 900 C in oxidizing atmosphere. Decomposition of PdO and Co 3 O 4 phases at high temperature, above 750 C, was observed. Moreover, sintering of Pd 0 and PdO particles along with of CoO crystallites takes place. (author)

High-temperature resistivity and thermoelectric properties of coupled substituted Ca3Co2O6

Directory of Open Access Journals (Sweden)

Meenakshisundaram Senthilkumar and Rajagopalan Vijayaraghavan

2009-01-01

Full Text Available Polycrystalline samples of Ca3−xNaxCo2−xMnxO6 (x=0.0–0.5 have been prepared by the sol-gel cum combustion method using sucrose in order to investigate the effects of the coupled substitution of Na and Mn on Ca and Co sites on the transport properties of Ca3Co2O6(Co326. The products were characterized by Fourier transform infrared spectroscopy, powder x-ray diffraction (XRD, thermogravimetry (TGA, differential thermal analysis and scanning electron microscopy. XRD patterns reveal the formation of single-phase products up to x=0.5. Coupled substitution increases the solubility of both Na and Mn on Ca and Co sites, respectively, in contrast to the limited solubility of Na and Mn (x=0.2 when separately substituted. TGA confirms the formation of the Ca3Co2O6 phase at temperatures ~720 °C. The grain size of the parent and substituted products is in the range 150–250 nm. Electrical resistivity and Seebeck coefficient were measured in the temperature range 300–800 K. Resistivity shows semiconducting behavior for all the compositions, particularly in the low-temperature regime. The Seebeck coefficient increases with temperature throughout the measured temperature range for all compositions. The maximum Seebeck coefficient (200 μV K−1 is observed for x=0.5 at 825 K, and this composition may be optimal for high-temperature thermoelectric applications.

Skeletal mineralogy of coral recruits under high temperature and pCO2

Science.gov (United States)

Foster, T.; Clode, P. L.

2016-03-01

Aragonite, which is the polymorph of CaCO3 precipitated by modern corals during skeletal formation, has a higher solubility than the more stable polymorph calcite. This higher solubility may leave animals that produce aragonitic skeletons more vulnerable to anthropogenic ocean acidification. It is therefore important to determine whether scleractinian corals have the plasticity to adapt and produce calcite in their skeletons in response to changing environmental conditions. Both high pCO2 and lower Mg / Ca ratios in seawater are thought to have driven changes in the skeletal mineralogy of major marine calcifiers in the past ˜ 540 Ma. Experimentally reduced Mg / Ca ratios in ambient seawater have been shown to induce some calcite precipitation in both adult and newly settled modern corals; however, the impact of high pCO2 on the mineralogy of recruits is unknown. Here we determined the skeletal mineralogy of 1-month-old Acropora spicifera coral recruits grown under high temperature (+3 °C) and pCO2 (˜ 900 µatm) conditions, using X-ray diffraction and Raman spectroscopy. We found that newly settled coral recruits produced entirely aragonitic skeletons regardless of the treatment. Our results show that elevated pCO2 alone is unlikely to drive changes in the skeletal mineralogy of young corals. Not having an ability to switch from aragonite to calcite precipitation may leave corals and ultimately coral reef ecosystems more susceptible to predicted ocean acidification. An important area for prospective research would be the investigation of the combined impact of high pCO2 and reduced Mg / Ca ratio on coral skeletal mineralogy.

Mathematical Modeling and Numerical Simulation of CO2 Removal by Using Hollow Fiber Membrane Contactors

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Mohammad Mesbah

2017-10-01

Full Text Available Abstract In this study, a mathematical model is proposed for CO2 separation from N2/CO2 mixtureusing a hollow fiber membrane contactor by various absorbents. The contactor assumed as non-wetted membrane; radial and axial diffusions were also considered in the model development. The governing equations of the model are solved via the finite element method (FEM. To ensure the accuracy of the developed model, the simulation results were validated using the reported experimental data for potassium glycinate (PG, monoethanol amine (MEA, and methyldiethanol amine (MDEA. The results of the proposed model indicated that PG absorbent has the highest removal efficiency of CO2, followed by potassium threonate (PT, MEA, amino-2-methyl-1-propanol (AMP, diethanol amine (DEA, and MDEA in sequence. In addition, the results revealed that the CO2 removal efficiency was favored by absorbent flow rate and liquid temperature, while the gas flow rate has a reverse effect. The simulation results proved that the hollow fiber membrane contactors have a good potential in the area of CO2 capture.

Flexible and High Performance Supercapacitors Based on NiCo2O4for Wide Temperature Range Applications

Science.gov (United States)

Gupta, Ram K.; Candler, John; Palchoudhury, Soubantika; Ramasamy, Karthik; Gupta, Bipin Kumar

2015-10-01

Binder free nanostructured NiCo2O4 were grown using a facile hydrothermal technique. X-ray diffraction patterns confirmed the phase purity of NiCo2O4. The surface morphology and microstructure of the NiCo2O4 analyzed by scanning electron microscopy (SEM) showed flower-like morphology composed of needle-like structures. The potential application of binder free NiCo2O4 as an electrode for supercapacitor devices was investigated using electrochemical methods. The cyclic voltammograms of NiCo2O4 electrode using alkaline aqueous electrolytes showed the presence of redox peaks suggesting pseudocapacitance behavior. Quasi-solid state supercapacitor device fabricated by sandwiching two NiCo2O4 electrodes and separating them by ion transporting layer. The performance of the device was tested using cyclic voltammetry, galvanostatic charge-discharge and electrochemical impedance spectroscopy. The device showed excellent flexibility and cyclic stability. The temperature dependent charge storage capacity was measured for their variable temperature applications. Specific capacitance of the device was enhanced by ~150% on raising the temperature from 20 to 60 °C. Hence, the results suggest that NiCo2O4 grown under these conditions could be a suitable material for high performance supercapacitor devices that can be operated at variable temperatures.

Effect of CO2 Flow Rate on the Pinang Frond-Based Activated Carbon for Methylene Blue Removal

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S. G. Herawan

2013-01-01

Full Text Available Activated carbons are regularly used the treatment of dye wastewater. They can be produced from various organics materials having high level of carbon content. In this study, a novel Pinang frond activated carbon (PFAC was produced at various CO2 flow rates in the range of 150–600 mL/min at activation temperature of 800°C for 3 hours. The optimum PFAC sample is found on CO2 flow rate of 300 mL/min which gives the highest BET surface area and pore volume of 958 m2/g and 0.5469 mL/g, respectively. This sample shows well-developed pore structure with high fixed carbon content of 79.74%. The removal of methylene blue (MB by 95.8% for initial MB concentration of 50 mg/L and 72.6% for 500 mg/L is achieved via this sample. The PFAC is thus identified to be a suitable adsorbent for removing MB from aqueous solution.

Elevated CO2-mitigation of high temperature stress associated with maintenance of positive carbon balance and carbohydrate accumulation in Kentucky bluegrass.

Science.gov (United States)

Song, Yali; Yu, Jingjin; Huang, Bingru

2014-01-01

Elevated CO2 concentration may promote plant growth while high temperature is inhibitory for C3 plant species. The interactive effects of elevated CO2 and high temperatures on C3 perennial grass growth and carbon metabolism are not well documented. Kentucky bluegrass (Poa pratensis) plants were exposed to two CO2 levels (400 and 800 μmol mol-1) and five temperatures (15/12, 20/17, 25/22, 30/27, 35/32°C, day/night) in growth chambers. Increasing temperatures to 25°C and above inhibited leaf photosynthetic rate (Pn) and shoot and root growth, but increased leaf respiration rate (R), leading to a negative carbon balance and a decline in soluble sugar content under ambient CO2. Elevated CO2 did not cause shift of optimal temperatures in Kentucky bluegrass, but promoted Pn, shoot and root growth under all levels of temperature (15, 20, 25, 30, and 35°C) and mitigated the adverse effects of severe high temperatures (30 and 35°C). Elevated CO2-mitigation of adverse effects of high temperatures on Kentucky bluegrass growth could be associated with the maintenance of a positive carbon balance and the accumulation of soluble sugars and total nonstructural carbohydrates through stimulation of Pn and suppression of R and respiratory organic acid metabolism.

Gas phase analysis of CO interactions with solid surfaces at high temperatures

International Nuclear Information System (INIS)

Anghel, Clara; Hoernlund, Erik; Hultquist, Gunnar; Limbaeck, Magnus

2004-01-01

An in situ method including mass spectrometry and labeled gases is presented and used to gain information on adsorption of molecules at high temperatures (>300 deg. C). Isotopic exchange rate in H 2 upon exposure to an oxidized zicaloy-2 sample and exchange rate in CO upon exposure to various materials have been measured. From these measurements, molecular dissociation rates in respective system have been calculated. The influence of CO and N 2 on the uptake rate of H 2 in zirconium and oxidized zicaloy-2 is discussed in terms of tendency for adsorption at high temperatures. In the case of oxidized Cr exposed to CO gas with 12 C, 13 C, 16 O and 18 O, the influence of H 2 O is investigated with respect to dissociation of CO molecules. The presented data supports a view of different tendencies for molecular adsorption of H 2 O, CO, N 2 , and H 2 molecules on surfaces at high temperatures

Evidence for divergence of response in Indica, Japonica, and wild rice to high CO2 x temperature interaction

Science.gov (United States)

Previous studies suggest that the intraspecific variability of rice yield response to rising carbon dioxide concentration, [CO2], could serve as a basis of selection to improve genotypes for future high CO2 conditions. However, assessment of responses to elevated [CO2] must consider air temperature,...

The effect of light supply on microalgal growth, CO2 uptake and nutrient removal from wastewater

International Nuclear Information System (INIS)

Gonçalves, A.L.; Simões, M.; Pires, J.C.M.

2014-01-01

Highlights: • Effect of irradiance and light:dark ratio on microalgal growth was analysed. • Microalgal growth, CO 2 capture, nitrogen and phosphorus uptake were evaluated. • Higher irradiances and light periods supported higher growth and CO 2 uptake rates. • All the studied microalgal strains have shown high nitrogen removal efficiencies. • The highest phosphorus removal efficiency was 67.6%. - Abstract: Microalgal based biofuels have been reported as an attractive alternative for fossil fuels, since they constitute a renewable energy source that reduces greenhouse gas emissions to the atmosphere. However, producing biofuels from microalgae is still not economically viable. Therefore, the integration of biofuel production with other microalgal applications, such as CO 2 capture and nutrient removal from wastewaters, would reduce the microalgal production costs (and the environmental impact of cultures), increasing the economic viability of the whole process. Additionally, producing biofuels from microalgae strongly depends on microalgal strain and culture conditions. This study evaluates the effect of culture conditions, namely light irradiance (36, 60, 120 and 180 μE m −2 s −1 ) and light:dark ratio (10:14, 14:10 and 24:0), on microalgal growth, atmospheric CO 2 uptake and nutrient (nitrogen and phosphorous) removal from culture medium. Four different microalgal strains, Chlorella vulgaris, Pseudokirchneriella subcapitata, Synechocystis salina and Microcystis aeruginosa, were studied to ascertain the most advantageous regarding the referred applications. This study has shown that higher light irradiance values and light periods resulted in higher specific growth rates and CO 2 uptake rates. C. vulgaris presented the highest specific growth rate and CO 2 uptake rate: 1.190 ± 0.041 d −1 and 0.471 ± 0.047 g CO2 L −1 d −1 , respectively. All the strains have shown high nitrogen removal efficiencies, reaching 100% removal percentages in

Interfacial tension measurement between CO2 and brines under high temperature and elevated pressure conditions

Science.gov (United States)

Li, X.; Boek, E. S.; Maitland, G. C.; Trusler, J. P. M.

2012-04-01

We have investigated the dependence of interfacial tension of (CO2 + brine) on temperature, pressure and salinity (including both salt type and molality) over the range of conditions applicable to CO2 storage in saline aquifers. The study covered a wide range of measurements of the interfacial tensions between carbon dioxide and (NaCl + KCl)(aq), CaCl2(aq), MgCl2(aq), Na2SO4(aq), KHCO3(aq), NaHCO3(aq) and two laboratory constructed brines with molality ranging from (0.3 to 5.0) mol·kg-1. The measurements were made at temperatures between (298 and 448) K at various pressures up to 50 MPa, using the pendant drop method in a high-pressure view cell filled with water-saturated CO2. The drop to be imaged was created by injecting brine from a high-pressure syringe pump into a capillary sealed through the top of the cell. The expanded uncertainties of the experimental state variables at 95 % confidence are +0.05 K in temperature and +70 kPa in pressure. For the interfacial tension, the overall expanded relative uncertainty at 95 % confidence was +1.6%. The experimental results show that interfacial tension for all the systems increases linearly with molality, indicating that relatively few measurements and simple interpolation procedures are adequate for describing this property accurately over wide ranges of conditions.

Development of activated carbon derived from banana peel for CO{sub 2} removal

Energy Technology Data Exchange (ETDEWEB)

Borhan, Azry; Thangamuthu, Subhashini; Ramdan, Amira Nurain [Chemical Engineering Department Universiti Teknologi PETRONAS, Bandar Seri Iskandar, 32610, Perak (Malaysia); Taha, Mohd Faisal [Fundamental and Applied Sciences Department Universiti Teknologi PETRONAS, Bandar Seri Iskandar, 32610, Perak (Malaysia)

2015-08-28

This research work highlights on the constraints involved in the preparation of the banana peel bio-sorbent, such as impregnation ratio, activation temperature and period of activation for reducing carbon dioxide (CO{sub 2}) in the atmosphere. Micromeritics ASAP 2020 and Field Emission Scanning Electron Microscope (FESEM) were used in identifying the best sample preparation method with the largest surface area which directly contributes to the effectiveness of adsorbent in removing CO{sub 2}. Sample A10 was identified to yield activated carbon with the largest surface area (260.3841 m{sup 2}/g), total pore volume (0.01638 cm{sup 3}/g) and pore diameter (0.2508 nm). Through nitrogen adsorption-desorption isotherm analysis, the existence of sub-micropores was proven when a combination of Type-I and Type-II isotherms were exhibited by the activated carbon produced. The results from the final adsorption test found that the material synthesized from the above mentioned parameter is capable of removing up to 1.65% wt of CO{sub 2} through adsorption at 25°C, suggesting that it can be effectively used as an adsorption material.

Matrix Transformation in Boron Containing High-Temperature Co-Re-Cr Alloys

Science.gov (United States)

Strunz, Pavel; Mukherji, Debashis; Beran, Přemysl; Gilles, Ralph; Karge, Lukas; Hofmann, Michael; Hoelzel, Markus; Rösler, Joachim; Farkas, Gergely

2018-03-01

An addition of boron largely increases the ductility in polycrystalline high-temperature Co-Re alloys. Therefore, the effect of boron on the alloy structural characteristics is of high importance for the stability of the matrix at operational temperatures. Volume fractions of ɛ (hexagonal close-packed—hcp), γ (face-centered cubic—fcc) and σ (Cr2Re3 type) phases were measured at ambient and high temperatures (up to 1500 °C) for a boron-containing Co-17Re-23Cr alloy using neutron diffraction. The matrix phase undergoes an allotropic transformation from ɛ to γ structure at high temperatures, similar to pure cobalt and to the previously investigated, more complex Co-17Re-23Cr-1.2Ta-2.6C alloy. It was determined in this study that the transformation temperature depends on the boron content (0-1000 wt. ppm). Nevertheless, the transformation temperature did not change monotonically with the increase in the boron content but reached a minimum at approximately 200 ppm of boron. A probable reason is the interplay between the amount of boron in the matrix and the amount of σ phase, which binds hcp-stabilizing elements (Cr and Re). Moreover, borides were identified in alloys with high boron content.

The development of an adsorbent for corrosion products in high-temperature water

International Nuclear Information System (INIS)

Kim, Yong Ik; Sung, Ki Woung; Kim, Kwang Rag; Kim, Yu Hwan; Koo, Jae Hyoo

1996-08-01

In order to use as adsorbent for removal of the soluble corrosion products, mainly Co 60 under PWR reactor coolant conditions (300 deg C, 160 kg/cm 2 ), stable ZrO 2 adsorbent was prepared using sol-gel process from zirconyl nitrate, AlO adsorbent was prepared by hydrolysis of aluminum isopropoxide, and titanium tetraisopropoxide, respectively. The prepared adsorbents were calcined at various temperature and analyzed by physical properties and the Co 2+ adsorption capacity. And it was shown that the Co 2+ adsorption capacity of the TiO 2 -Al 2 O 3 adsorbents were found to have larger than that of ZrO 2 and Al 2 O 3 adsorbents in high-temperature water. ZrO 2 , Al 2 O 3 and TiO 2 -Al 2 O 3 adsorbents were found to be suitable high-temperature adsorbents for the removal of dissolved corrosion products, mainly Co in PWR reactor coolant conditions. 15 tabs., 51 figs., 55 refs. (Author)

Effects of water vapor pretreatment time and reaction temperature on CO(2) capture characteristics of a sodium-based solid sorbent in a bubbling fluidized-bed reactor.

Science.gov (United States)

Seo, Yongwon; Jo, Sung-Ho; Ryu, Chong Kul; Yi, Chang-Keun

2007-10-01

CO(2) capture from flue gas using a sodium-based solid sorbent was investigated in a bubbling fluidized-bed reactor. Carbonation and regeneration temperature on CO(2) removal was determined. The extent of the chemical reactivity after carbonation or regeneration was characterized via (13)C NMR. In addition, the physical properties of the sorbent such as pore size, pore volume, and surface area after carbonation or regeneration were measured by gas adsorption method (BET). With water vapor pretreatment, near complete CO(2) removal was initially achieved and maintained for about 1-2min at 50 degrees C with 2s gas residence time, while without proper water vapor pretreatment CO(2) removal abruptly decreased from the beginning. Carbonation was effective at the lower temperature over the 50-70 degrees C temperature range, while regeneration more effective at the higher temperature over the 135-300 degrees C temperature range. To maintain the initial 90% CO(2) removal, it would be necessary to keep the regeneration temperature higher than about 135 degrees C. The results obtained in this study can be used as basic data for designing and operating a large scale CO(2) capture process with two fluidized-bed reactors.

Corrosion Behaviors of Structural Materials in High Temperature S-CO{sub 2} Environments

Energy Technology Data Exchange (ETDEWEB)

Lee, Ho Jung; Kim, Hyunmyung; Jang, Changheui [KAIST, Daejeon (Korea, Republic of)

2014-04-15

The isothermal corrosion tests of several types of stainless steels, Ni-based alloys, and ferritic-martensitic steels (FMS) were carried out at the temperature of 550 and 650 .deg. C in SFR S-CO{sub 2} environment (200 bar) for 1000 h. The weight gain was greater in the order of FMSs, stainless steels, and Ni-based alloys. For the FMSs (Fe-based with low Cr content), a thick outer Fe oxide, a middle (Fe,Cr)-rich oxide, and an inner (Cr,Fe)-rich oxide were formed. They showed significant weight gains at both 550 and 650 .deg. C. In the case of austenitic stainless steels (Fe-based) such as SS 316H and 316LN (18 wt.% Cr), the corrosion resistance was dependent on test temperatures except SS 310S (25 wt.% Cr). After corrosion test at 650 .deg. C, a large increase in weight gain was observed with the formation of outer thick Fe oxide and inner (Cr,Fe)-rich oxide. However, at 550 .deg. C, a thin Cr-rich oxide was mainly developed along with partially distributed small and nodular shaped Fe oxides. Meanwhile, for the Ni-based alloys (16-28 wt.% Cr), a very thin Cr-rich oxide was developed at both test temperatures. The superior corrosion resistance of high Cr or Ni-based alloys in the high temperature S-CO{sub 2} environment was attributed to the formation of thin Cr-rich oxide on the surface of the materials.

Determining the high variability of pCO2 and pO2 in the littoral zone of a subtropical coastal lake

Directory of Open Access Journals (Sweden)

Denise Tonetta

2014-09-01

Full Text Available The aquatic metabolism comprises production and mineralization of organic matter through biological processes, such as primary production and respiration that can be estimated by gases concentration in the water column. AIM: The study aimed to assess the temporal variability of pCO2 and pO2 in the littoral zone of a subtropical coastal lake. Our hypotheses are i high variability in meteorological conditions, such as temperature and light, drive the high variability in pCO2 and pO2, and ii the lake is permanently heterotrophic due to the low phosphorus concentration. METHODS: We estimated pCO2 from pH-alkalinity method, and pO2 from dissolved oxygen concentration and water temperature measured in free-water during 24 hours in the autumn, winter, spring and summer. RESULTS: Our findings showed that limnological variables had low temporal variability, while the meteorological variables and pCO2 presented a high coefficient of variation, which is representative of each climatic season. In autumn and winter, it was recorded that the lake was supersaturated in CO2 relative to the atmosphere, while in spring and summer CO2 concentration was below the concentration found in the atmosphere. Over 24 hours, pCO2 also showed high variability, with autumn presenting higher concentration during the night when compared to daytime. Water temperature and chlorophyll a were negatively correlated with pCO2, while pO2 was positively correlated with wind and light. CONCLUSION: Agreeing with our first hypothesis, pCO2 showed an expressive temporal variation in a subtropical lake associated to the high variability in meteorological conditions. On the other hand, our second hypothesis was not confirmed, since Peri Lake exported CO2 to the atmosphere in some periods and in others, CO2 was removed from the atmosphere.

Red soil as a regenerable sorbent for high temperature removal of hydrogen sulfide from coal gas

International Nuclear Information System (INIS)

Ko, T.-H.; Chu Hsin; Lin, H.-P.; Peng, C.-Y.

2006-01-01

In this study, hydrogen sulfide (H 2 S) was removed from coal gas by red soil under high temperature in a fixed-bed reactor. Red soil powders were collected from the northern, center and southern of Taiwan. They were characterized by XRPD, porosity analysis and DCB chemical analysis. Results show that the greater sulfur content of LP red soils is attributed to the higher free iron oxides and suitable sulfidation temperature is around 773 K. High temperature has a negative effect for use red soil as a desulfurization sorbent due to thermodynamic limitation in a reduction atmosphere. During 10 cycles of regeneration, after the first cycle the red soil remained stable with a breakthrough time between 31 and 36 min. Hydrogen adversely affects sulfidation reaction, whereas CO exhibits a positive effect due to a water-shift reaction. COS was formed during the sulfidation stage and this was attributed to the reaction of H 2 S and CO. Results of XRPD indicated that, hematite is the dominant active species in fresh red soil and iron sulfide (FeS) is a product of the reaction between hematite and hydrogen sulfide in red soils. The spinel phase FeAl 2 O 4 was found during regeneration, moreover, the amount of free iron oxides decreased after regeneration indicating the some of the free iron oxide formed a spinel phase, further reducting the overall desulfurization efficiency

Performance evaluation of high-sulphur coal-fired USC plant integrated with SNOX and CO2 capture sections

International Nuclear Information System (INIS)

Cau, Giorgio; Tola, Vittorio; Bassano, Claudia

2015-01-01

In recent years coal-fired power plants have increased their role in the global energy scenario thanks to reliability, security of fuel supply and lower cost of fuel and electricity. In this framework global warming issues require a sustainable use of coal and great efforts for greenhouse gases reduction, addressing research and development projects towards more efficient solutions in terms of efficiency and environmental impact. With this aim in this paper a performance assessment of an Ultra Super Critical (USC) steam plant integrated with a CO 2 removal section was carried out. The study is based on simulation models specifically developed through Aspen-Plus and Gate-Cycle software platforms. Performance was assessed referring to typical USC commercial size plants (400–600 MW), fuelled by a mix of a low-sulphur coal and a Sardinian (Sulcis) high-sulphur coal. The USC plant, based on a reheated and regenerative Rankine cycle, is integrated with an SNOX section, with integrated DeNO x and DeSO x processes, and a low temperature CO 2 capture section. The SNOX technology shows several advantages in comparison to conventional de-nitrification and de-sulphuration systems. In particular it is capable to remove both nitrogen and sulphur oxides, requiring less energy absorption compared to traditional FGD systems, allowing a further preheating of the combustion air and without producing process waste. Besides the SNOX releases a commercial product as the sulphuric acid (H 2 SO 4 ) and operational costs are reduced when sulphur content in the coal increases. The CO 2 capture system was based on a chemical absorption process. A conventional system based on an amine (monoethanolamine, MEA) aqueous solution was considered. In order to match high pressure and purity CO 2 transportation requirements, the CO 2 removal section is also integrated with a conditioning and compression section. A performance assessment of the USC plant was carried out varying the high-sulphur coal

High temperature capture of CO2 on lithium-based sorbents from rice husk ash.

Science.gov (United States)

Wang, Ke; Guo, Xin; Zhao, Pengfei; Wang, Fanzi; Zheng, Chuguang

2011-05-15

Highly efficient Li(4)SiO(4) (lithium orthosilicate)-based sorbents for CO(2) capture at high temperature, was developed using waste materials (rice husk ash). Two treated rice husk ash (RHA) samples (RHA1 and RHA2) were prepared and calcined at 800°C in the presence of Li(2)CO(3). Pure Li(4)SiO(4) and RHA-based sorbents were characterized by X-ray fluorescence, X-ray diffraction, scanning electron microscopy, nitrogen adsorption, and thermogravimetry. CO(2) sorption was tested through 15 carbonation/calcination cycles in a fixed bed reactor. The metals of RHA were doped with Li(4)SiO(4) resulting to inhibited growth of the particles and increased pore volume and surface area. Thermal analyses indicated a much better CO(2) absorption in Li(4)SiO(4)-based sorbent prepared from RHA1 (higher metal content sample) because the activation energies for the chemisorption process and diffusion process were smaller than that of pure Li(4)SiO(4). RHA1-based sorbent also maintained higher capacities during the multiple cycles. Copyright © 2011 Elsevier B.V. All rights reserved.

CO2 reduction potential of future coal gasification based power generation technologies

International Nuclear Information System (INIS)

Jansen, D.; Oudhuis, A.B.J.; Van Veen, H.M.

1992-03-01

Assessment studies are carried out on coal gasification power plants integrated with gas turbines (IGCC) or molten carbonate fuel cells (MCFC) without and with CO 2 -removal. System elements include coal gasification, high-temperature gas-cleaning, molten carbonate fuel cells or gas turbines, CO shift, membrane separation, CO 2 recovery and a bottoming cycle. Various system configurations are evaluated on the basis of thermodynamic computations. The energy balances of the various system configurations clearly indicate that integrated coal gasification MCFC power plants (IGMCFC) with CO 2 removal have high efficiencies (42-47% LHV) compared to IGCC power plants with CO 2 -removal (33-38% LHV) and that the CO 2 -removal is simplified due to the specific properties of the molten carbonate fuel cells. IGMCFC is therefore an option with future prospective in the light of clean coal technologies for power generation with high energy efficiencies and low emissions. 2 figs., 3 tabs., 10 refs

Influence of Temperature on the Performance of LiNi1/3Co1/3Mn1/3O2 Prepared by High-Temperature Ball-Milling Method

Directory of Open Access Journals (Sweden)

Ming Tian

2018-01-01

Full Text Available Aiming at the preparation of high electrochemical performance LiNi1/3Co1/3Mn1/3O2 cathode material for lithium-ion battery, LiNi1/3Co1/3Mn1/3O2 was prepared with lithium carbonate, nickel (II oxide, cobalt (II, III oxide, and manganese dioxide as raw materials by high-temperature ball-milling method. Influence of ball-milling temperature was investigated in this work. It was shown that the fine LiNi1/3Co1/3Mn1/3O2 powder with high electrochemical performance can be produced by the high-temperature ball-milling process, and the optimal ball-milling temperature obtained in the current study was 750°C. Its initial discharge capacity was 146.0 mAhg−1 at the rate of 0.1 C, and over 50 cycles its capacity retention rate was 90.2%.

Removal of dogs' gingival pigmentation with CO2 laser

Science.gov (United States)

Figueiredo, Jose A. P.; Chavantes, Maria C.; Gioso, Marco A.; Pesce, Hildeberto F.; Jatene, Adib D.

1995-05-01

The aim of this study was to analyze the ability of CO2 laser to remove physiologic pigmentation of gingiva. Dogs were chosen for this study because of their intense black pigmentation on the gingiva, similar to what can be found in human negroes and other dark- skinned races. Three specimens were irradiated at the left side of the buccal aspect of the gingiva, while for comparison the right side was used as a control. CO2 laser in a continuous mode applying 3 watt power was used (Xanar-20, USA). The portion to be irradiated was continuously irrigated with saline solution, to prevent tissue damage from the excessive heat generated. The handpiece device irradiated the target easily and fast, with no bleeding. All the pigmentation could be removed from the portion exposed to the laser beam. A 45th day follow up showed very little repigmentation just in one of the specimens. It could be concluded that CO2 laser irradiation can be an alternative to remove pigmentation of the gingiva for cosmetic purposes. The risk of repigmentation exists, so the patients should be aware of this inconvenience, sometimes demanding further irradiation.

Trace and low concentration co2 removal methods and apparatus utilizing metal organic frameworks

KAUST Repository

Eddaoudi, Mohamed

2016-03-10

In general, this disclosure describes techniques for removing trace and low concentration CO2 from fluids using SIFSIX-n-M MOFs, wherein n is at least two and M is a metal. In some embodiments, the metal is zinc or copper. Embodiments include devices comprising SIFSIX-n-M MOFs for removing CO2 from fluids. In particular, embodiments relate to devices and methods utilizing SIFSIX-n-M MOFs for removing CO2 from fluids, wherein CO2 concentration is trace. Methods utilizing SIFSIX-n-M MOFs for removing CO2 from fluids can occur in confined spaces. SIFSIX-n-M MOFs can comprise bidentate organic ligands. In a specific embodiment, SIFSIX-n-M MOFs comprise pyrazine or dipryidilacetylene ligands.

Preparation of ZnO/SiO{sub 2} gel composites and their performance of H{sub 2}S removal at room temperature

Energy Technology Data Exchange (ETDEWEB)

Liu, Guoqiang [Laboratory of Advanced Materials, Department of Materials Science and Engineering, Tsinghua University, Beijing 100084 (China); Huang, Zheng-Hong, E-mail: zhhuang@tsinghua.edu.cn [Laboratory of Advanced Materials, Department of Materials Science and Engineering, Tsinghua University, Beijing 100084 (China); Kang, Feiyu [Laboratory of Advanced Materials, Department of Materials Science and Engineering, Tsinghua University, Beijing 100084 (China); Institute of Advanced Materials Research, Graduate School at Shenzhen, Tsinghua University, Shenzhen 518055 (China)

2012-05-15

Graphical abstract: The ZnO/SiO{sub 2} gel composites exhibit mixed type isotherms, in which the initial part is type I, and intermediate and high relative pressures are type IV with a hysteresis loop of type H2. The breakthrough time of ZnO/SiO{sub 2} composites first increased sharply up to 400 Degree-Sign C with the H{sub 2}S breakthrough capacity is up to 96.4 mg/g, and then decrease dramatically with further rising of temperature beyond 500 Degree-Sign C. Highlights: Black-Right-Pointing-Pointer High surface area ZnO/SiO{sub 2} gel composites were prepared by co-sol-gel method. Black-Right-Pointing-Pointer The active phase (ZnO) well disperses in the composites. Black-Right-Pointing-Pointer The highest H{sub 2}S adsorption capacity of the composites reaches up to 96.4 mg/g. Black-Right-Pointing-Pointer Both physisorption and the active phase reactivation governed the H{sub 2}S removal process. - Abstract: ZnO/SiO{sub 2} gel composites with different active component loading were prepared by sol-gel method combined with ambient drying process, followed by thermal treatment. The gel composites were characterized by scanning electron microscopy (SEM), nitrogen adsorption, X-ray diffraction (XRD), FTIR and X-ray photoelectron spectroscopy (XPS), and their performances for H{sub 2}S removal were evaluated by dynamic testing at room temperature. The as prepared materials exhibited high surface area with multimodal pore size distributions in micropore and mesopore region. The porous properties were significantly influenced both by the ZnO loading ratio and the treated temperature. The gel composites showed a high performance for H{sub 2}S removal, with the highest H{sub 2}S adsorption capacity of 96.4 mg/g for the sample treated at 400 Degree-Sign C with 30 wt% ZnO. Both physisorption and the active phase reactivation governed the H{sub 2}S removal process. It needs to optimize the composites' porous structure and active component loading amount.

In situ X-ray ptychography imaging of high-temperature CO2 acceptor particle agglomerates

DEFF Research Database (Denmark)

Høydalsvik, Kristin; Fløystad, Jostein Bø; Zhao, Tiejun

2014-01-01

be used for in situ phase contrast imaging in structure studies at atmospheric pressure and elevated temperatures. Lithium zirconate, a candidate CO2 capture material, was studied at a pressure of one atmosphere in air and in CO2, at temperatures exceeding 600 °C. Images with a spatial resolution better...

Reactivity in the removal of SO{sub 2} and NO{sub x} on Co/Mg/Al mixed oxides derived from hydrotalcites

Energy Technology Data Exchange (ETDEWEB)

Palomares, A.E. [Department of Chemical and Nuclear Engineering, Universidad Politecnica Valencia, Avda. de los Naranjos s/n, 46022 Valencia (Spain); Lopez-Nieto, J.M.; Corma, A. [Instituto de Tecnologia Quimica, UPV-CSIC, Universidad Politecnica de Valencia, Avenida de los Naranjos s/n., 46022 Valencia (Spain); Lazaro, F.J.; Lopez, A. [Instituto Ciencia de Materiales de Aragon (CSIC- Universidad de Zaragoza), 50015 Zaragoza (Spain)

1999-04-05

Metal containing hydrotalcites, where metal oxides present redox properties and hydrotalcite shows a basic character, appear to be new important environmental catalysts for the removal of SO{sub x} and NO{sub x}. Redox and basic properties of a mixed Co/Mg/Al oxide derived from hydrotalcites are tuned in order to achieve the optimal catalytic behavior required. This sample has been characterized showing that cobalt is present in two forms, as isolated and well dispersed paramagnetic ions, and as very small Co-containing particles (in the nanometric range), with an internal antiferromagnetic ordering at low temperature. The redox properties of cobalt allow the reduction of NO with propane at high temperatures and in presence of oxygen. The reduced cobalt species are proposed as the active sites. Nevertheless, for the removal of SO{sub 2} and contrary to the case of Cu/Mg/Al samples, the addition of an oxidant as cerium oxide on Co/Mg/Al is necessary in order to oxidize SO{sub 2} to SO{sub 3}. In this case, similar results than those obtained with previously reported catalyst, i.e. cerium or copper-cerium hydrotalcite, are obtained. These results indicate that this catalyst could be an adequate material for the simultaneous removal of SO{sub 2} and NO{sub x} in a FCC unit

Evidence for a temperature-induced spin-state transition of Co3+ in La2-xSrxCoO4

Science.gov (United States)

Hollmann, N.; Haverkort, M. W.; Benomar, M.; Cwik, M.; Braden, M.; Lorenz, T.

2011-05-01

We study the magnetic susceptibility of mixed-valent La2-xSrxCoO4 single crystals in the doping range of 0.5⩽x⩽0.8 for temperatures up to 1000 K. The magnetism below room temperature is described by paramagnetic Co2+ in the high-spin state and by Co3+ in the nonmagnetic low-spin state. At high temperatures, an increase in susceptibility is seen, which we attribute to a temperature-induced spin-state transition of Co3+. The susceptibility is analyzed by comparison to full-multiplet calculations for the thermal population of the high- and intermediate-spin states of Co3+.

Thermophysical and radiation properties of high-temperature C4F8-CO2 mixtures to replace SF6 in high-voltage circuit breakers

Science.gov (United States)

Zhong, Linlin; Cressault, Yann; Teulet, Philippe

2018-03-01

C4F8-CO2 mixtures are one of the potential substitutes to SF6 in high-voltage circuit breakers. However, the arc quenching ability of C4F8-CO2 mixtures is still unknown. In order to provide the necessary basic data for the further investigation of arc quenching performance, the compositions, thermodynamic properties, transport coefficients, and net emission coefficients (NEC) of various C4F8-CO2 mixtures are calculated at temperatures of 300-30 000 K in this work. The thermodynamic properties are presented as the product of mass density and specific heat, i.e., ρCp. The transport coefficients include electrical conductivity, viscosity, and thermal conductivity. The atomic and molecular radiation are both taken into account in the calculation of NEC. The comparison of the properties between SF6 and C4F8-CO2 mixtures is also discussed to find their differences. The results of compositions show that C4F8-CO2 mixtures have a distinctive advantage over other alternative gases e.g., CF3I and C3F8, because the dissociative product (i.e., C4F6) of C4F8 at low temperatures has a very high dielectric strength. This is good for an arc quenching medium to endure the arc recovery phase. Compared with SF6, C4F8-CO2 mixtures present lower ρCp at temperatures below 2800 K and larger thermal conductivity above 2800 K. Based on the position of peaks in thermal conductivity, we predict that the cooling of C4F8-CO2 arc will be slowed down at higher temperatures than that of SF6 arc. It is also found that the mixing of CO2 shows slight effects on the electrical conductivity and NEC of C4F8-CO2 mixtures.

Tritium removal by CO2 laser heating

International Nuclear Information System (INIS)

Skinner, C.H.; Kugel, H.; Mueller, D.

1997-01-01

Efficient techniques for rapid tritium removal will be necessary for ITER to meet its physics and engineering goals. One potential technique is transient surface heating by a scanning CO 2 or Nd:Yag laser that would release tritium without the severe engineering difficulties of bulk heating of the vessel. The authors have modeled the heat propagation into a surface layer and find that a multi-kW/cm 2 flux with an exposure time of order 10 ms is suitable to heat a 50 micron co-deposited layer to 1,000--2,000 degrees. Improved wall conditioning may be a significant side benefit. They identify remaining issues that need to be addressed experimentally

Tritium removal by CO2 laser heating

International Nuclear Information System (INIS)

Skinner, C.H.; Kugel, H.; Mueller, D.

1997-10-01

Efficient techniques for rapid tritium removal will be necessary for ITER (International Thermonuclear Experimental Reactor) to meet its physics and engineering goals. One potential technique is transient surface heating by a scanning CO 2 or Nd:YAG laser that would release tritium without the severe engineering difficulties of bulk heating of the vessel. The authors have modeled the heat propagation into a surface layer and find that a multi-kW/cm 2 flux with an exposure time of order 10 msec is suitable to heat a 50 micron co-deposited layer to 1,000--2,000 degrees. Improved wall conditioning may be a significant side benefit. They identify remaining issues that need to be addressed experimentally

High temperature oxidation behaviour of nanostructured cermet coatings in a mixed CO2 - O2 environment

Science.gov (United States)

Farrokhzad, M. A.; Khan, T. I.

2014-06-01

Nanostructured ceramic-metallic (cermet) coatings composed of nanosized ceramic particles (α-Al2O3 and TiO2) dispersed in a nickel matrix were co-electrodeposited and then oxidized at 500°C, 600°C and 700°C in a mixed gas using a Thermo-gravimetric Analysis (TGA) apparatus. The mixed gas was composed of 15% CO2, 10% O2 and 75% N2. This research investigates the effects of CO2 and O2 partial pressures on time-depended oxidation rates for coatings and compared them to the results from atmospheric oxidation under similar temperatures. The increase in partial pressure of oxygen due to the presence of CO2 at each tested temperature was calculated and correlated to the oxidation rate of the coatings. The results showed that the presence of CO2 in the system increased the oxidation rate of cermet coatings when compared to atmospheric oxidation at the same temperature. It was also shown that the increase in the oxidation rate is not the result of CO2 acting as the primary oxidant but as a secondary oxidant which results in an increase of the total partial pressure of oxygen and consequently higher oxidation rates. The WDS and XRD analyses results showed that the presence of nanosized TiO2 particles in a nickel matrix can improve oxidation behaviour of the coatings by formation of Ni-Ti compounds on oxidizing surface of the coating which was found beneficiary in reducing the oxidation rates for cermet coatings.

LMFBR Emergency Deployment Assuming 45 year Time-Delay Excess CO2 Removal

International Nuclear Information System (INIS)

Schenewerk, William Ernest

2008-01-01

Atmospheric CO 2 is presently increasing 2.25% per year in proportion to 2.25% per year exponential fossil fuel consumption increase. CO 2 removal is modeled as being proportional to 45-year-earlier CO 2 amount above 280 ppmV-C. This is: Exp (-0.0225/year * 45 years) = 0.36 fraction CO 2 removed from anthropological emissions, apparently by seawater. LMFBRs use 15 year doubling time. Deploying 30000 GWe atomic power by year-2080 results in CO 2 doubling year-2065 if World primary energy consumption continues increasing 2.25% per year. CO 2 remains roughly twice pre-industrial until year-2100. Beginning year-2080, CO 2 declines at 2.25% per year. CO 2 will presumably decline back to roughly the year-2000 value by year-2200 if the 45-year-delay sink remains effective. LMFBR and GCFR fleet expands to 30000 GWe by 2080. 1000 GWe LWR fleet consumes 5 Mt HM (Heavy Metal). Breeder first cores require 1 Mt HM. (author)

Potential high temperature corrosion problems due to co-firing of biomass and fossil fuels

DEFF Research Database (Denmark)

Montgomery, Melanie; Vilhelmsen, T.; Jensen, S.A.

2007-01-01

Over the past years, considerable high temperature corrosion problems have been encountered when firing biomass in power plants due to the high content of potassium chloride in the deposits. Therefore to combat chloride corrosion problems co-firing of biomass with a fossil fuel has been undertaken....... This results in potassium chloride being converted to potassium sulphate in the combustion chamber and it is sulphate rich deposits that are deposited on the vulnerable metallic surfaces such as high temperature superheaters. Although this removes the problem of chloride corrosion, other corrosion mechanisms...... appear such as sulphidation and hot corrosion due to sulphate deposits. At Studstrup power plant Unit 4, based on trials with exposure times of 3000 hours using 0-20% straw co-firing with coal, the plant now runs with a fuel of 10% straw + coal. After three years exposure in this environment...

Isoreticular rare earth fcu-MOFs for the selective removal of H 2 S from CO 2 containing gases

KAUST Repository

Bhatt, Prashant

2017-05-04

In this work, we present the implementation of reticular chemistry and the molecular building block approach to unveil the appropriateness of Rare Earth (RE) based Metal-Organic Frameworks (MOFs) with fcu topology for H2S removal applications. Markedly, RE-fcu-MOFs, having different pore apertures sizes in the range of 4.7-6.0 Å and different functionalities, showed excellent properties for the removal of H2S from CO2 and CH4 containing gases such as natural gas, biogas and landfill gas. A series of cyclic mixed gas breakthrough experiments were carried out on three isoreticular fcu-MOFs, containing linkers of different lengths (between 8.4 and 5 Å), by using simulated natural gas mixture containing CO2/H2S/CH4 (5%/5%/90%) under different adsorption and regeneration conditions. The fcu-MOF platform has good H2S removal capacity with a high H2S/CO2 selectivity, outperforming benchmark materials like activated carbon and Zeolites in many aspects. The comparison of H2S removal performance with the related structures of the RE-fcu-MOFs provides insightful information to shed light on the relationship between the structural features of the MOF and its associated H2S separation properties. The excellent H2S/CO2 and H2S/CH4 selectivity of these materials offer great prospective for the production of pure H2S, with acceptable levels of CO2for Claus process to produce elemental sulfur.

Inactivation of Bacillus subtilis spores by high pressure CO2 with high temperature.

Science.gov (United States)

Rao, Lei; Xu, Zhenzhen; Wang, Yongtao; Zhao, Feng; Hu, Xiaosong; Liao, Xiaojun

2015-07-16

The objective of this study was to investigate the inactivation of the Bacillus subtilis spores by high pressure CO2 combined with high temperature (HPCD+HT) and to analyze the clumping effect of the spores on their HPCD+HT resistance. The spores of B. subtilis were subjected to heat at 0.1 MPa and HPCD at 6.5-25 MPa, and 82 °C, 86 °C, and 91 °C for 0-120 min. The spores were effectively inactivated by HPCD+HT, but a protective effect on the spores was also found, which was closely correlated to the pressure, temperature and time. The spores treated by HPCD+HT at 6.5 and 10 MPa exhibited a two-stage inactivation curve of shoulder and log-linear regions whereas the spores at 15-25 MPa exhibited a three-stage inactivation curve of shoulder, log-linear and tailing regions, and these curves were well fitted to the Geeraerd model. Approximately 90% of pyridine-2,6-dicarboxylic acid (DPA) was released after HPCD+HT and the 90% DPA release time depend on the pressure and temperature. Moreover, the spore clumping in suspensions was examined by dynamic light scattering. The particle size of the spore suspensions increased with the increase of pressure, temperature and time, indicating the spore clumping. 0.1% Tween 80 as a surfactant inhibited the spore clumping and increased the inactivation ratio of the spores by HPCD+HT. These results indicated that the spore clumping enhanced the spores' resistance to HPCD+HT and induced a protective effect. Copyright © 2015 Elsevier B.V. All rights reserved.

The development of an adsorbent for corrosion products in high-temperature water

Energy Technology Data Exchange (ETDEWEB)

Kim, Yong Ik; Sung, Ki Woung; Kim, Kwang Rag; Kim, Yu Hwan; Koo, Jae Hyoo [Korea Atomic Energy Research Institute, Taejon (Korea, Republic of)

1996-08-01

In order to use as adsorbent for removal of the soluble corrosion products, mainly Co{sup 60} under PWR reactor coolant conditions (300 deg C, 160 kg/cm{sup 2}), stable ZrO{sub 2} adsorbent was prepared using sol-gel process from zirconyl nitrate, AlO adsorbent was prepared by hydrolysis of aluminum isopropoxide, and titanium tetraisopropoxide, respectively. The prepared adsorbents were calcined at various temperature and analyzed by physical properties and the Co{sup 2+} adsorption capacity. And it was shown that the Co{sup 2+} adsorption capacity of the TiO{sub 2}-Al{sub 2}O{sub 3} adsorbents were found to have larger than that of ZrO{sub 2} and Al{sub 2}O{sub 3} adsorbents in high-temperature water. ZrO{sub 2}, Al{sub 2}O{sub 3} and TiO{sub 2}-Al{sub 2}O{sub 3} adsorbents were found to be suitable high-temperature adsorbents for the removal of dissolved corrosion products, mainly Co in PWR reactor coolant conditions. 15 tabs., 51 figs., 55 refs. (Author).

Removal of CO2 in closed loop off-gas treatment systems

International Nuclear Information System (INIS)

Clemens, M.K.; Nelson, P.A.; Swift, W.M.

1994-01-01

A closed loop test system has been installed at Argonne National Laboratory (ANL) to demonstrate off-gas treatment, absorption, and purification systems to be used for incineration and vitrification of hazardous and mixed waste. Closed loop systems can virtually eliminate the potential for release of hazardous or toxic materials to the atmosphere during both normal and upset conditions. In initial tests, a 250,000 Btu/h (75 kW thermal) combustor was operated in an open loop to produce a combustion product gas. The CO 2 in these tests was removed by reaction with a fluidized bed of time to produce CaCO 3 . Subsequently, recirculation system was installed to allow closed loop operation with the addition of oxygen to the recycle stream to support combustion. Commercially marketed technologies for removal of CO 2 can be adapted for use on closed loop incineration systems. The paper also describes the Absorbent Solution Treatment (AST) process, based on modifications to commercially demonstrated gas purification technologies. In this process, a side loop system is added to the main loop for removing CO 2 in scrubbing towers using aqueous-based CO 2 absorbents. The remaining gas is returned to the incinerator with oxygen addition. The absorbent is regenerated by driving off the CO 2 and water vapor, which are released to the atmosphere. Contaminants are either recycled for further treatment or form precipitates which are removed during the purification and regeneration process. There are no direct releases of gases or particulates to the environment. The CO 2 and water vapor go through two changes of state before release, effectively separating these combustion products from contaminants released during incineration. The AST process can accept a wide range of waste streams. The system may be retrofitted to existing Facilities or included in the designs for new installations

Nonionic Fluorinated Surfactant Removal from Mesoporous Film Using sc-CO2.

Science.gov (United States)

Chavez Panduro, Elvia A; Assaker, Karine; Beuvier, Thomas; Blin, Jean-Luc; Stébé, Marie-José; Konovalov, Oleg; Gibaud, Alain

2017-01-25

Surfactant templated silica thin films were self-assembled on solid substrates by dip-coating using a partially fluorinated surfactant R 8 F (EO) 9 as the liquid crystal template. The aim was 2-fold: first we checked which composition in the phase diagram was corresponding to a 2D rectangular highly ordered crystalline phase and second we exposed the films to sc-CO 2 to foster the removal of the surfactant. The films were characterized by in situ X-ray reflectivity (XRR) and grazing incidence small angle X-ray scattering (GISAXS) under CO 2 pressure from 0 to 100 bar at 34 °C. GISAXS patterns reveal the formation of a 2-D rectangular structure at a molar ratio R 8 F (EO) 9 /Si equal to 0.1. R 8 F (EO) 9 micelles have a cylindrical shape, which have a core/shell structure ordered in a hexagonal system. The core contains the R 8 F part and the shell is a mixture of (EO) 9 embedded in the silica matrix. We further evidence that the extraction of the template using supercritical carbon dioxide can be successfully achieved. This can be attributed to both the low solubility parameter of the surfactants and the fluorine and ethylene oxide CO 2 -philic groups. The initial 2D rectangular structure was well preserved after depressurization of the cell and removal of the surfactant. We attribute the very high stability of the rinsed film to the large value of the wall thickness relatively to the small pore size.

Innovative CO2 LASER-Based Pavement Striping and Stripe Removal

Science.gov (United States)

2014-07-01

This is a Technical Report of an FY2014 NDOT funded project on Innovative CO2 Laserbased Pavement Striping and Stripe Removal. The project was concerned with adopting the laser technology for pavement stripe and markers removal and inferring on its e...

Application of banana peels waste as adsorbents for the removal of CO2, NO, NOx, and SO2 gases from motorcycle emissions

Science.gov (United States)

Viena, V.; Elvitriana; Wardani, S.

2018-03-01

The aims of the study were to investigate the application of banana peels as adsorbent for the removal of CO, NO, NOx and SO2 gases from motorcycles emissions. The effect of differents thermal activation on the characteristics of banana peels adsorbent (BPA) such as moisture content, ash content, volatile matter and fixed carbon has been studied using proximate analysis. The study of Iodine adsorption capacity of BPA was obtained at 952 mg/g adsorbent. Structure and morphology of BPA were characterized by Fourier transform infrared (FTIR) and field emission scanning electron microscopy (SEM). The results showed that BPA could significantly adsorbed the CO and SO2 gases emissions from motorcycles, but not applicable for NO, NOx gases. After 10 minutes of flue gas analysis at idle mode using BPA adsorption tube, CO gas could be totally removed, from initial 19618 ppm to 0 ppm, while SO2 gas could also be totally removed from 24523 ppm to 0 ppm. SEM test showed that temperature of activation had significant effect on the size of pores of BPA formed. BPA was suitable for application in removing CO and SO2 gases emissions from motorcycles and it helps to reduce the green house gas effects of fossil fuel to the environment.

Analysis and study on the membrane method of CO2 removal of coal-fired boilers

International Nuclear Information System (INIS)

Fangqin, Li; Henan, Li; Jianxing, Ren; Jiang, Wu; Zhongzhu, Qiu

2010-01-01

Carbon dioxide (CO 2 ) is one kind of harmful substances from the burning process of fossil fuel. CO 2 emissions cause serious pollution on atmospheric environment, especially greenhouse effect. In this paper, CO 2 formation mechanism and control methods were researched. Membrane technology was studied to control CO 2 emissions from coal-fired boilers. The relationship between CO 2 removal efficiency and parameters of membrane contactor was analyzed. Through analysis and study, factors affecting on CO 2 removal efficiency were gotten. How to choose the best parameters was known. This would provide theoretical basis for coal-fired utility boilers choosing effective way of CO 2 removal. (author)

CO2 removals and CO2 and non-CO2 trace gas emissions affected by human activity in the forests in the Republic of macedonia

International Nuclear Information System (INIS)

Grupche, Ljupcho; Lozanovski, Risto; Markovska, Natasha

2001-01-01

During 2000 and 2001 inventories of CO 2 removals and emissions caused by changes in forest and other woody biomass stocks, as well as the inventories of CO 2 and non-CO 2 trace gas emissions caused by forest conversions (accidental burning) were carried out. According to the forest area in ha, and depending on the differences between the annual biomass increment and annual biomass consumption, about 30-50% of total annual carbon uptake increment is released through the biomass consumption from stocks. 50-70% of the net annual carbon uptake converted to CO 2 identify the annual removals of this gas, which is on average 1805 Gg/yr, ranging between 1485 and 2243 Gg/yr. From 1990 to 1998 on average 4700 ha forest area (min. 110 ha in 1991, max. 14420 ha in 1993) was burned. Proportionally to the burned area, there was a release on average of 18.62 kt C annually (min. 0.42 kt C, max. 57.11 kt), related to 136.07 kt CO 2 on average (min. 1.5 kt CO 2 , max. 209.22 kt CO 2 ). (Original)

Effectiveness of carbon dioxide removal in lowering atmospheric CO2 and reversing global warming in the context of 1.5 degrees

Science.gov (United States)

Zickfeld, K.; Azevedo, D.

2017-12-01

The majority of emissions scenarios that limit warming to 2°C, and nearly all emission scenarios that do not exceed 1.5°C warming by the year 2100 require artificial removal of CO2 from the atmosphere. Carbon dioxide removal (CDR) technologies in these scenarios are required to offset emissions from sectors that are difficult or costly to decarbonize and to generate global `net negative' emissions, allowing to compensate for earlier emissions and to meet long-term climate stabilization targets after overshoot. Only a few studies have explored the Earth system response to CDR and large uncertainties exist regarding the effect of CDR on the carbon cycle and its effectiveness in reversing climate impacts after overshoot. Here we explore the effectiveness of CDR in lowering atmospheric CO2 ("carbon cycle effectiveness") and cool global climate ("cooling effectiveness"). We force the University of Victoria Earth System Climate Model, a model of intermediate complexity, with a set of negative CO2 emissions pulses of different magnitude and applied from different background atmospheric CO2 concentrations. We find the carbon cycle effectiveness of CDR - defined as the change in atmospheric CO2 per unit CO2 removed - decreases with the amount of CO2 removed from the atmosphere and increases at higher background CO2 concentrations from which CDR is applied due to nonlinear responses of carbon sinks to CO2 and climate. The cooling effectiveness - defined as the change in global mean surface air temperature per unit CO2 removed - on the other hand, is largely insensitive to the amount of CO2 removed, but decreases if CDR is applied at higher atmospheric CO2 concentrations, due to the logarithmic relationship between atmospheric CO2 and radiative forcing. Based on our results we conclude that CDR is more effective in restoring a lower atmospheric CO2 concentration and reversing impacts directly linked to CO2 at lower levels of overshoot. CDR's effectiveness in restoring a

Temperature changes across CO2-lased dentin during multiple exposures

Science.gov (United States)

Zakariasen, Kenneth L.; Barron, Joseph R.; Boran, Thomas L.

1990-06-01

The literature increasingly indicates that lasers will have a multitude of applications for dental hard tissue procedures, e.g. preventive therapy, caries removal, laser etching and endodontic therapy. However, it is critical that such laser therapies avoid the production of heat levels which will be damaging to the surrounding vital tissues, such as the dental pulp and periodontal tissues. Our preliminary research on temperature changes across C02 lased dentin indicated that for single preventive therapeutic exposures (1.2 W., 0. 1 sec., 1.0 mm focal spot) the mean temperature rise across 350 j.tm of dentin was 0.57 0C while across 1000 .tm of dentin the mean rise was only 0.18 °C. Further research utilizing multiple preventive therapeutic exposures (1.2 W., 0. 1 sec., 1.0 mm focal spot, 3 x 1.0 sec. intervals) showed mean temperature elevations of 1.56 0C across 350 m of dentin and 0.66 O across 1000 xm of dentin. While these temperature elevations, which would be associated with preventive therapy, are very low and would be biologically acceptable, it must be noted that exposures of higher intensities are required to fuse enamel and porcelain, or remove decay. This current research investigates temperature elevations which occuT during C02 lasing utilizing the following exposure parameters: 8.0 W., 1.0 mm focal spot, 0.1 sec. exposures, 2 or 4 exposures per site pulsed 1.0 sec. apart. Three dentin thicknesses were utilized, i.e. 1000 jim, 1500 p.tm and 2000 .tm. Four sections of each thickness were utilized with four exposure sites per specimen (2 with 2 exposures, 2 with 4 exposures). All dentin sections were prepared from non-carious third molars using a hard tissue microtome. A thermistor was placed on the dentin surface opposite each lased site and temperature changes were recorded for approximately 50 sec. following lasing. Mean temperature elevations ranged from a high of 3.07 C for the 1000 xm section utilizing four exposures to a low of 0.37 0C for the

A feasible process for simultaneous removal of CO2, SO2 and NOx in the cement industry by NH3 scrubbing

International Nuclear Information System (INIS)

Dong, Ruifeng; Lu, Hongfang; Yu, Yunsong; Zhang, Zaoxiao

2012-01-01

Highlights: ► Simultaneous removal of CO 2 , SO 2 and NO x is realized by NH 3 scrubbing with NaClO 2 . ► The crystallization process of NH 4 HCO 3 is employed instead of CO 2 regeneration. ► Energy consumption reduces hugely while CO 2 removal rate remains higher than 90%. ► Exergy calculation reveals that a higher thermodynamic perfection degree is achieved. -- Abstract: With the rapid economic and industrial development, the concentration of carbon dioxide in the atmosphere is increasing enormously, which has greatly affected the global climate and human living environment. At present, a lot of technologies have been applied to CO 2 removal in fossil fuel-fired power plants, which are one of the main CO 2 emission sources. But few researches have been done in the cement industry, which is the third largest CO 2 emission source. There is no mature technology of CO 2 removal in cement industry mentioned before. This paper proposes a feasible process for simultaneous removal of CO 2 , SO 2 and NO x in the cement industry by NH 3 scrubbing. As there is no ready steam source for the regeneration of CO 2 -rich loading solvent after absorption, a process with the final product of ammonium bicarbonate is developed. With the oxidative additive of NaClO 2 added in the aqueous ammonium absorbent, the simultaneous removal of CO 2 , SO 2 and NO x is feasible by NH 3 scrubbing. The products of the process are mainly ammonium bicarbonate, ammonium sulfate and ammonium nitrate, which are all good fertilizers for crops and plants. The crystallization of NH 4 HCO 3 is easier for storage and transportation than that for liquid carbon dioxide, which becomes more stable when dicyandiamide (DCD) is added. The thermodynamic analysis proves that the proposed process has the advantages of energy conservation and high thermodynamic perfection degree compared with the traditional ones.

Carbon dioxide removal with inorganic membranes

Energy Technology Data Exchange (ETDEWEB)

Judkins, R.R.; Fain, D.E. [Oak Ridge National Laboratory, TN (United States)

1993-12-31

The increasing concentrations of greenhouse gases, particularly carbon dioxide, in the atmosphere has sparked a great deal of interest in the removal of CO{sub 2} from flue gases of fossil fueled plants. Presently, several techniques for the removal of CO{sub 2} are considered to have potential, but are lacking in practicality. For example, amine scrubbing of flue gas streams is potential, but are lacking in practically. For example, amine scrubbing of flue gas streams is effective in removing CO{sub 2}, but costs are high; efficiency suffers; and other acid gases must be removed prior to amine stripping. Membrane systems for CO{sub 2} removal are held in high regard, and inorganic, particularly ceramic, membranes offer the potential for high temperature, thus energy saving, removal.

Optimization of a cascade refrigeration system using refrigerant C_3H_8 in high temperature circuits (HTC) and a mixture of C_2H_6/CO_2 in low temperature circuits (LTC)

International Nuclear Information System (INIS)

Nasruddin; Sholahudin, S.; Giannetti, N.; Arnas

2016-01-01

Highlights: • Multi-objective optimization is conducted in the cascade refrigeration system. • Combination of operating temperature and refrigerant performance has been studied. • Characteristic of C_3H_8 and a mixture of C_2H_6/CO_2 have been investigated. • Determining of CO_2 fraction to optimize refrigeration system has been done. - Abstract: This paper discusses the multi-objectives optimization of a cascade refrigeration system using refrigerant C_3H_8 in high temperature circuits (HTC) and a mixture of C_2H_6/CO_2 in low temperature circuits (LTC). The evaporator temperature, condenser temperature, C_2H_6/CO_2 mixture condensation temperature, cascade temperature differences, and the CO_2 mass fraction are chosen as the decision variables. Whereas cooling capacity, cold space temperature, and ambient temperature are taken as the constraints. The purpose of this research is to design a cascade refrigeration system whose optimum performance are defined in terms of economics and thermodynamics. Accordingly, there are two objective functions that should be simultaneously optimized including the total annual cost which consists of the capital and operational cost and the total exergy destruction of the system. To this aim, the optimum operating temperature of the system and CO_2 fraction should be determined so that the system has minimum exergy destruction and annual cost. Results show that, the optimum value of the decision variables for this system can be determined by trade-off between annual cost and exergy destruction.

A rod-packing microporous hydrogen-bonded organic framework for highly selective separation of C2H2/CO2at room temperature

KAUST Repository

Li, Peng

2014-11-13

Self-assembly of a trigonal building subunit with diaminotriazines (DAT) functional groups leads to a unique rod-packing 3D microporous hydrogen-bonded organic framework (HOF-3). This material shows permanent porosity and demonstrates highly selective separation of C2H2/CO2 at ambient temperature and pressure.

A rod-packing microporous hydrogen-bonded organic framework for highly selective separation of C2H2/CO2at room temperature

KAUST Repository

Li, Peng; He, Yabing; Zhao, Yunfeng; Weng, Linhong; Wang, Hailong; Krishna, Rajamani A A; Wu, Hui; Zhou, Wei; O'Keeffe, Michael A.; Han, Yu; Chen, Banglin

2014-01-01

Self-assembly of a trigonal building subunit with diaminotriazines (DAT) functional groups leads to a unique rod-packing 3D microporous hydrogen-bonded organic framework (HOF-3). This material shows permanent porosity and demonstrates highly selective separation of C2H2/CO2 at ambient temperature and pressure.

H + CH{sub 2}CO {yields} CH{sub 3} + CO at high temperature : a high pressure chemical activation reaction with positive barrier.

Energy Technology Data Exchange (ETDEWEB)

Hranisavljevic, J.; Kumaran, S. S.; Michael, J. V.

1997-12-08

The Laser Photolysis-Shock Tube (LP-ST) technique coupled with H-atom atomic resonance absorption spectrometry (ARAS) has been used to study reaction, H + CH{sub 2}CO {r_arrow} CH{sub 3} + CO, over the temperature range, 863-1400 K. The results can be represented by the Arrhenius expression, k = (4.85 {+-} 0.70) x 10{sup {minus}11} exp({minus}2328 {+-} 155 K/T) cm{sup 3} molecule{sup {minus}1} s{sup {minus}1}. The present data have been combined with the earlier low temperature flash photolysis-resonance fluorescence measurements to yield a joint three parameter expression, k = 5.44 x 10{sup {minus}14} T{sup 0.8513} exp({minus}1429 K/T) cm{sup 3} molecule{sup {minus}1} s{sup {minus}1}. This is a chemical activation process that proceeds through vibrationally excited acetyl radicals. However, due to the presence of a low lying forward dissociation channel to CH{sub 3} + CO, the present results refer to the high pressure limiting rate constants. Hence, transition state theory with Eckart tunneling is used to explain the data.

Mathematical Analysis of High-Temperature Co-electrolysis of CO2 and O2 Production in a Closed-Loop Atmosphere Revitalization System

Energy Technology Data Exchange (ETDEWEB)

Michael G. McKellar; Manohar S. Sohal; Lila Mulloth; Bernadette Luna; Morgan B. Abney

2010-03-01

NASA has been evaluating two closed-loop atmosphere revitalization architectures based on Sabatier and Bosch carbon dioxide, CO2, reduction technologies. The CO2 and steam, H2O, co-electrolysis process is another option that NASA has investigated. Utilizing recent advances in the fuel cell technology sector, the Idaho National Laboratory, INL, has developed a CO2 and H2O co-electrolysis process to produce oxygen and syngas (carbon monoxide, CO and hydrogen, H2 mixture) for terrestrial (energy production) application. The technology is a combined process that involves steam electrolysis, CO2 electrolysis, and the reverse water gas shift (RWGS) reaction. A number of process models have been developed and analyzed to determine the theoretical power required to recover oxygen, O2, in each case. These models include the current Sabatier and Bosch technologies and combinations of those processes with high-temperature co-electrolysis. The cases of constant CO2 supply and constant O2 production were evaluated. In addition, a process model of the hydrogenation process with co-electrolysis was developed and compared. Sabatier processes require the least amount of energy input per kg of oxygen produced. If co-electrolysis replaces solid polymer electrolyte (SPE) electrolysis within the Sabatier architecture, the power requirement is reduced by over 10%, but only if heat recuperation is used. Sabatier processes, however, require external water to achieve the lower power results. Under conditions of constant incoming carbon dioxide flow, the Sabatier architectures require more power than the other architectures. The Bosch, Boudouard with co-electrolysis, and the hydrogenation with co-electrolysis processes require little or no external water. The Bosch and hydrogenation processes produce water within their reactors, which aids in reducing the power requirement for electrolysis. The Boudouard with co-electrolysis process has a higher electrolysis power requirement because carbon

Photocatalytic oxidation removal of Hg"0 using ternary Ag/AgI-Ag_2CO_3 hybrids in wet scrubbing process under fluorescent light

International Nuclear Information System (INIS)

Zhang, Anchao; Zhang, Lixiang; Chen, Xiaozhuan; Zhu, Qifeng; Liu, Zhichao; Xiang, Jun

2017-01-01

Highlights: • Ag/AgI-Ag_2CO_3 hybrids were employed for Hg"0 removal under fluorescent light. • Superoxide radical (·O_2"−) played a key role in Hg"0 removal. • NO exhibited a significant effect on Hg"0 removal in comparison to SO_2. • The mechanism for enhanced Hg"0 removal over Ag/AgI-Ag_2CO_3 was proposed. - Abstract: A series of ternary Ag/AgI-Ag_2CO_3 photocatalysts synthesized using a facile coprecipitation method were employed to investigate their performances of Hg"0 removal in a wet scrubbing reactor. The hybrids were characterized by N_2 adsorption-desorption, XRD, SEM-EDS, HRTEM, XPS, DRS and ESR. The photocatalytic activities of Hg"0 removal were evaluated under fluorescent light. The results showed that AgI content, fluorescent light irradiation, reaction temperature all showed significant influences on Hg"0 removal. NO exhibited significant effect on Hg"0 removal in comparison to SO_2. Among these ternary Ag/AgI-Ag_2CO_3 hybrids, Ag/AgI(0.1)-Ag_2CO_3 showed the highest Hg"0 removal efficiency, which could be ascribed to the effective separation of photogenerated electron-hole pairs between AgI and Ag_2CO_3 and the surface plasmon resonance (SPR) effect in the visible region by metallic silver nanoparticles (Ag"0 NPs). The trapping studies of reactive radicals showed that the superoxide radicals (·O_2"−) may play a key role in Hg"0 removal under fluorescent light. According to the experimental and characterization results, a possible photocatalytic oxidation mechanism for enhanced Hg"0 removal over Ag/AgI(0.1)-Ag_2CO_3 hybrid under fluorescent light was proposed.

High temperature oxidation behaviour of nanostructured cermet coatings in a mixed CO2 – O2 environment

International Nuclear Information System (INIS)

Farrokhzad, M A; Khan, T I

2014-01-01

Nanostructured ceramic-metallic (cermet) coatings composed of nanosized ceramic particles (α-Al 2 O3 and TiO 2 ) dispersed in a nickel matrix were co-electrodeposited and then oxidized at 500°C, 600°C and 700°C in a mixed gas using a Thermo-gravimetric Analysis (TGA) apparatus. The mixed gas was composed of 15% CO 2 , 10% O 2 and 75% N 2 . This research investigates the effects of CO 2 and O 2 partial pressures on time-depended oxidation rates for coatings and compared them to the results from atmospheric oxidation under similar temperatures. The increase in partial pressure of oxygen due to the presence of CO 2 at each tested temperature was calculated and correlated to the oxidation rate of the coatings. The results showed that the presence of CO 2 in the system increased the oxidation rate of cermet coatings when compared to atmospheric oxidation at the same temperature. It was also shown that the increase in the oxidation rate is not the result of CO2 acting as the primary oxidant but as a secondary oxidant which results in an increase of the total partial pressure of oxygen and consequently higher oxidation rates. The WDS and XRD analyses results showed that the presence of nanosized TiO 2 particles in a nickel matrix can improve oxidation behaviour of the coatings by formation of Ni-Ti compounds on oxidizing surface of the coating which was found beneficiary in reducing the oxidation rates for cermet coatings

Forest soil CO2 fluxes as a function of understory removal and N-fixing species addition.

Science.gov (United States)

Li, Haifang; Fu, Shenglei; Zhao, Hongting; Xia, Hanping

2011-01-01

We report on the effects of forest management practices of understory removal and N-fixing species (Cassia alata) addition on soil CO2 fluxes in an Eucalyptus urophylla plantation (EUp), Acacia crassicarpa plantation (ACp), 10-species-mixed plantation (Tp), and 30-species-mixed plantation (THp) using the static chamber method in southern China. Four forest management treatments, including (1) understory removal (UR); (2) C. alata addition (CA); (3) understory removal and replacement with C. alata (UR+CA); and (4) control without any disturbances (CK), were applied in the above four forest plantations with three replications for each treatment. The results showed that soil CO2 fluxes rates remained at a high level during the rainy season (from April to September), followed by a rapid decrease after October reaching a minimum in February. Soil CO2 fluxes were significantly higher (P plantations under various management practices.

Removal of foreign bodies in children's airways using flexible bronchoscopic CO2 cryotherapy.

Science.gov (United States)

Zhang, Lei; Yin, Yong; Zhang, Jing; Zhang, Hao

2016-09-01

The present retrospective study investigated the safety and efficacy of removing foreign bodies from children's airways using flexible bronchoscopic CO2 cryotherapy instead of traditional foreign body aspiration. Between October 2012 and June 2014 in the Shanghai Children's Medical Center, we performed flexible bronchoscopic CO2 cryotherapy to remove foreign bodies from the airways of 12 children who ranged in age from 10 to 40 months and analyzed outcomes and complications. Using cryotherapy, we successfully and without complications removed the foreign bodies in eight of 12 children. In two cases, the foreign bodies were removed successfully, but cryotherapy partially damaged the airway mucosa, which caused partial airway obstruction because of the newly developed granulation tissue. We incompletely removed the foreign body in one case and failed to remove the foreign body in another case. No serious adverse reactions or complications were observed after the treatments. Removal of foreign bodies from children's airways using flexible bronchoscopic CO2 cryotherapy may be a safe, easy, and effective method. Pediatr Pulmonol. 2016; 51:943-949. © 2016 Wiley Periodicals, Inc. © 2016 Wiley Periodicals, Inc.

Low-temperature CO oxidation over Cu/Pt co-doped ZrO2 nanoparticles synthesized by solution combustion.

Science.gov (United States)

Singhania, Amit; Gupta, Shipra Mital

2017-01-01

Zirconia (ZrO 2 ) nanoparticles co-doped with Cu and Pt were applied as catalysts for carbon monoxide (CO) oxidation. These materials were prepared through solution combustion in order to obtain highly active and stable catalytic nanomaterials. This method allows Pt 2+ and Cu 2+ ions to dissolve into the ZrO 2 lattice and thus creates oxygen vacancies due to lattice distortion and charge imbalance. High-resolution transmission electron microscopy (HRTEM) results showed Cu/Pt co-doped ZrO 2 nanoparticles with a size of ca. 10 nm. X-ray diffraction (XRD) and Raman spectra confirmed cubic structure and larger oxygen vacancies. The nanoparticles showed excellent activity for CO oxidation. The temperature T 50 (the temperature at which 50% of CO are converted) was lowered by 175 °C in comparison to bare ZrO 2 . Further, they exhibited very high stability for CO reaction (time-on-stream ≈ 70 h). This is due to combined effect of smaller particle size, large oxygen vacancies, high specific surface area and better thermal stability of the Cu/Pt co-doped ZrO 2 nanoparticles. The apparent activation energy for CO oxidation is found to be 45.6 kJ·mol -1 . The CO conversion decreases with increase in gas hourly space velocity (GHSV) and initial CO concentration.

The potential effects of concurrent increases in temperature, CO2 and O3 on net photosynthesis, as mediated by rubisCO

International Nuclear Information System (INIS)

Long, S.; Essex Univ., Colchester

1992-07-01

At the leaf level, under light saturating and light limiting conditions, it is shown that elevated atmospheric CO 2 concentration not only alters the scale of the response of carbon gain to rising temperature, but can alter the direction of response. These points bring into serious question the value of any predictions of plant production which ignore not only the direct effect Of C0 2 on carbon gain, but also the basic interactions of temperature, C0 2 and 0 3 . Whilst many factors may potentially diminish the enhancement of lightsaturated leaf photosynthetic rates with increase in atmospheric CO 2 concentrations, no mechanism has so far been identified which could remove the parallel stimulation of light-limited photosynthesis

The interactive effects of elevated CO2, temperature and N supply on rice yield

International Nuclear Information System (INIS)

Baysa, Marieta C.; Tremmel, David C.; Reynolds, James F.; Rivero, Gilda C.; Tabbada, Reynaldo A.

2001-01-01

Rice (Oryza sativa L. cv. IR 72)was grown in growth chambers under combinations of two CO 2 (375 and 750 μL L -1 ), temperature(29/21 and 34/26 degrees centigrade day/night) and N (40 and 80 mg L -1 ) regimes from sowing until grain maturity. Panicle production was significantly enhanced by elevated CO 2 with more pronounced effects at high temperature and N. CO 2 -enriched plants grown at high temperatures had lower harvest indices due to reductions in the number of grains per panicle and grain mass. Any potential benefit of increased atmospheric CO 2 on rice grain yield and grain N content under optimal N supply may therefore be dampened by higher temperatures associated with possible future global warming conditions. (Author)

Efficient TEA CO2 laser based coating removal system

CSIR Research Space (South Africa)

Prinsloo, FJ

2007-04-01

Full Text Available stream_source_info Prinsloo_2007.pdf.txt stream_content_type text/plain stream_size 11617 Content-Encoding UTF-8 stream_name Prinsloo_2007.pdf.txt Content-Type text/plain; charset=UTF-8 Efficient TEA CO2 laser based... by keeping energy density below the damage threshold. The advantage of a pulsed TEA CO2 laser system is that a laser frequency and temporal profile can be chosen to maximize paint removal and concurrently minimize substrate damage. To achieve...

High temperature oxidation behaviour of nanostructured cermet coatings in amixed CO/sub 2/ - O/sub 2/ environment

International Nuclear Information System (INIS)

Farrokhzad, M. A.; Khan, T. I.

2013-01-01

Nanostructured ceramic-metallic (cermet) coatings composed of nanosized ceramic particles (alpha-Al /sub 2/O/sub 3/ and TiO/sub 2/) dispersed in a nickel matrix were co-electrodeposited and then oxidized at 500 degree C, 600 degree C and 700 degree C in a mixed gas using a Thermo-gravimetric Analysis (TGA) apparatus. The mixed gas was composed of 15 percentage CO/sub 2/, 10 percentage O/sub 2/ and 75 percentage N/sub 2/. This research investigates the effects of CO/sub 2/ and O/sub 2/ partial pressures on time-depended oxidation rates for coatings and compared them to the results from atmospheric oxidation under similar temperatures. The increase in partial pressure of oxygen due to the presence of CO/sub 2/ at each tested temperature was calculated and correlated to the oxidation rate of the coatings. The results showed that the presence of CO/sub 2/ in the system increased the oxidation rate of cermet coatings when compared to atmospheric oxidation at the same temperature. It was also shown that the increase in the oxidation rate is not the result of CO/sub 2/ acting as the primary oxidant but as a secondary oxidant which results in an increase of the total partial pressure of oxygen and consequently higher oxidation rates. The WDS and XRD analyses results showed that the presence of nanosized TiO/sub 2/ particles in a nickel matrix can improve oxidation behaviour of the coatings by formation of Nu i-Tau i compounds on oxidizing surface of the coating which was found beneficiary in reducing the oxidation rates for cermet coatings. (author)

Experimental Analysis of the Effects of CO and CO2 on High Temperature PEM Fuel Cell Performance using Electrochemical Impedance Spectroscopy

DEFF Research Database (Denmark)

Andreasen, Søren Juhl; Vang, Jakob Rabjerg

2010-01-01

The use of high temperature PEM (HTPEM) fuel cells running on reformate gas shows comparable performance to HTPEM fuel cells running on pure hydrogen, even when running at high levels of CO, as long as high operating temperatures are ensured. The increased operating temperatures of these types of...

High Temperature PEM Fuel Cell Performance Characterisation with CO and CO₂ using Electrochemical Impedance Spectroscopy

DEFF Research Database (Denmark)

Andreasen, Søren Juhl; Vang, Jakob Rabjerg; Kær, Søren Knudsen

2011-01-01

at different temperatures, currents, and different content of CO, CO2 and H2 in the anode gas. The impedance spectrum at each operating point is fitted to an equivalent circuit and an analysis to identify the different mechanisms governing the impedance is performed. The trends observed, when varying...

High-capacity NO2 denuder systems operated at various temperatures (298-473 K).

Science.gov (United States)

Wolf, Jan-Christoph; Niessner, Reinhard

2012-12-01

In this study, we investigated several coatings for high-temperature, high-capacity, and high-efficiency denuder-based NO(2) removal, with the scope to face the harsh conditions and requirements of automotive exhaust gas sampling. As first coating, we propose a potassium iodide (KI)/polyethylene glycol coating with a high removal efficiency (ε > 98%) for about 2 h and 50 ppm NO(2) at room temperature (298 K). At elevated temperatures (423 K), the initial capacity (100 ppmh) is decreased to 15 ppmh. Furthermore, this is the first proposal of the ionic liquid methyl-butyl-imidazolium iodide ([BMIm(+)][I(-)]) as denuder coating material. At room temperature, this ionic liquid exhibits far greater capacity (300 ppmh) and NO(2) removal efficiency (ε > 99.9%) than KI. Nevertheless, KI exhibits a slightly (~10%) higher capacity at elevated temperatures than [BMIm(+)][I(-)]. Both coatings presented are suitable for applications requiring selective denuding of NO(2) at temperatures up to 423 K.

CO2 and humidity removal system for extended Shuttle missions - Equilibrium testing and performance analysis

Science.gov (United States)

Davis, S. H.; Kissinger, L. D.

1976-01-01

In Shuttle orbiter cabins, lithium hydroxide (LiOH) canisters are currently planned to be used for CO2 adsorption and condensing heat exchangers for humidity control. In this paper a more effective CO2 and humidity removal method is proposed by replacing the LiOH component with HS-C adsorbent (a polyethylenimine coated acrylic ester), thus eliminating the low temperature constraints on the active thermal control system. Since the adsorption of CO2 and H2O are reversible, a double bed configuration operating cyclicly is planned to provide continuous atmospheric control. Apparatus and the experimental procedure to test the adsorption equilibrium are described and some of the indicative results, tabulated by computers, are presented with the help of exponential expressions and differential equations. By using a computer model of the Shuttle HS-C system, performance predictions are made.

Effect of Promoter Concentration on CO2 Separation Using K2CO3 With Reactive Absorption Method in Reactor Packed Column

Directory of Open Access Journals (Sweden)

Monde Junety

2018-01-01

Full Text Available The presence of carbon dioxide (CO2 in the gas is not expected because CO2 can reduce heating value and CO2 is the major emission contributor into the atmosphere. Various separation technologies can be used to reduce CO2 content and improve quality of gas. Chemical or reactive absorption is most widely used because it provides higher removal rate. This paper will study the effect of the addition di ethanolamine (DEA concentration into aqueous 30wt.% potassium carbonate(K2CO3 with reactive absorption method in a reactor packed column at temperature from 40°C to 80°C, DEA concentration range of (1% - 3% and absorbent flow rate (0.5, 0.75 and 1 L. min1. Contacting the gas and absorbent are countercurrent flow in packed column with 1.5 m high and 50 mm in diameter. The absorption column was randomly packed with a packing material raschig rings 5 mm in diameter. The CO2 loading in the liquid samples was determined by titration. It is found that the best result of CO2 loading is 0.065594 mole/mole K2CO3 and CO2 removal 28%. The result show that the loading capacity (mole CO2/mole K2CO3 and CO2 removal increased with the increase of DEA concentration.

High temperature deformation mechanisms of L12-containing Co-based superalloys

Science.gov (United States)

Titus, Michael Shaw

Ni-based superalloys have been used as the structural material of choice for high temperature applications in gas turbine engines since the 1940s, but their operating temperature is becoming limited by their melting temperature (Tm =1300degrees C). Despite decades of research, no viable alternatives to Ni-based superalloys have been discovered and developed. However, in 2006, a ternary gamma' phase was discovered in the Co-Al-W system that enabled a new class of Co-based superalloys to be developed. These new Co-based superalloys possess a gamma-gamma' microstructure that is nearly identical to Ni-based superalloys, which enables these superalloys to achieve extraordinary high temperature mechanical properties. Furthermore, Co-based alloys possess the added benefit of exhibiting a melting temperature of at least 100degrees C higher than commercial Ni-based superalloys. Superalloys used as the structural materials in high pressure turbine blades must withstand large thermomechanical stresses imparted from the rotating disk and hot, corrosive gases present. These stresses induce time-dependent plastic deformation, which is commonly known as creep, and new superalloys must possess adequate creep resistance over a broad range of temperature in order to be used as the structural materials for high pressure turbine blades. For these reasons, this research focuses on quantifying high temperature creep properties of new gamma'-containing Co-based superalloys and identifying the high temperature creep deformation mechanisms. The high temperature creep properties of new Co- and CoNi-based alloys were found to be comparable to Ni-based superalloys with respect to minimum creep rates and creep-rupture lives at 900degrees C up to the solvus temperature of the gamma' phase. Co-based alloys exhibited a propensity for extended superlattice stacking fault formation in the gamma' precipitates resulting from dislocation shearing events. When Ni was added to the Co-based compositions

Investigations and researches on CO2 balance in a high-temperature carbon dioxide separation technology; Nisanka tanso koon bunri gijutsu ni okeru CO2 balance ni kansuru chosa kenkyu

Energy Technology Data Exchange (ETDEWEB)

NONE

1996-03-01

With an objective to select a promising process by comparing application environments and effectiveness of a high-temperature carbon dioxide separation, recovery and re-utilization technology with other methods, investigations were performed on reducible amount of carbon dioxide discharge by using material balance and system introduction. A large number of chemical and physical technologies are being developed for the separation and refining methods. This paper discusses the technologies for their application to iron and steel making, oil refining, and petrochemical industries, the so-called heavy and large product industries. As a possibility of utilizing the high-temperature separated CO2 in iron and steel making, an investigation was given on the direct iron ore smelting reduction process. It would be unreasonable to use CO2 in oil refining as a substitute to air to regenerate a catalytic decomposition and reformation catalyst because of decline in the catalytic activity. A discussion was given on a case to replace steam with CO2 in steam reformation and pyrolysis of hydrocarbons. The discussion requires the objective to be focused on such items as C/H ratio at a reformer outlet and relationship of balance in decomposition products. The C1 chemical and others were reviewed to search possibilities for their use as raw materials of chemicals used in chemical industries. Possibilities were discussed to fix high-temperature CO2 into peridotite and serpentine. 42 refs., 32 figs., 11 tabs.

Acidic sweep gas with carbonic anhydrase coated hollow fiber membranes synergistically accelerates CO2 removal from blood.

Science.gov (United States)

Arazawa, D T; Kimmel, J D; Finn, M C; Federspiel, W J

2015-10-01

The use of extracorporeal carbon dioxide removal (ECCO2R) is well established as a therapy for patients suffering from acute respiratory failure. Development of next generation low blood flow (carbonic anhydrase (CA) immobilized bioactive hollow fiber membrane (HFM) which significantly accelerates CO2 removal from blood in model gas exchange devices by converting bicarbonate to CO2 directly at the HFM surface. This present study tested the hypothesis that dilute sulfur dioxide (SO2) in oxygen sweep gas could further increase CO2 removal by creating an acidic microenvironment within the diffusional boundary layer adjacent to the HFM surface, facilitating dehydration of bicarbonate to CO2. CA was covalently immobilized onto poly (methyl pentene) (PMP) HFMs through glutaraldehyde activated chitosan spacers, potted in model gas exchange devices (0.0151 m(2)) and tested for CO2 removal rate with oxygen (O2) sweep gas and a 2.2% SO2 in oxygen sweep gas mixture. Using pure O2 sweep gas, CA-PMP increased CO2 removal by 31% (258 mL/min/m(2)) compared to PMP (197 mL/min/m(2)) (Premoval by 17% (230 mL/min/m(2)) compared to pure oxygen sweep gas control (Premoval increased by 109% (411 mL/min/m(2)) (Premoval, and when used in combination with bioactive CA-HFMs has a synergistic effect to more than double CO2 removal while maintaining physiologic pH. Through these technologies the next generation of intravascular and paracorporeal respiratory assist devices can remove more CO2 with smaller blood contacting surface areas. A clinical need exists for more efficient respiratory assist devices which utilize low blood flow rates (removal efficiency by shifting equilibrium from bicarbonate to gaseous CO2, through either a bioactive carbonic anhydrase enzyme coating or bulk blood acidification with lactic acid. In this study we demonstrate a novel approach to local blood acidification using an acidified sweep gas in combination with a bioactive coating to more than double CO2 removal

Interactive effect of elevated CO2 and temperature on coral physiology

Science.gov (United States)

Grottoli, A. G.; Cai, W.; Warner, M.; Melman, T.; Schoepf, V.; Baumann, J.; Matsui, Y.; Pettay, D. T.; Hoadley, K.; Xu, H.; Wang, Y.; Li, Q.; Hu, X.

2011-12-01

Increases in ocean acidification and temperature threaten coral reefs globally. However, the interactive effect of both lower pH and higher temperature on coral physiology and growth are poorly understood. Here, we present preliminary findings from a replicated controlled experiment where four species of corals (Acorpora millepora, Pocillopora damicornis, Montipora monasteriata, Turbinaria reniformis) were reared under the following six treatments for three weeks: 1) 400ppm CO2 and ambient temperature, 2) 400ppm CO2 and elevated temperature, 3) 650ppm CO2 and ambient temperature, 4) 650ppm CO2 and elevated temperature, 5) 800ppm CO2 and ambient temperature, 6) 800ppm CO2 and elevated temperature. Initial findings of photophysiological health (Fv/Fm), calcification rates (as measured by both buoyant weight and the total alkalinity methods), and energy reserves will be presented.

The High Accuracy Measurement of CO2 Mixing Ratio Profiles Using Ground Based 1.6 μm CO2-DIAL with Temperature Measurement Techniques in the Lower-Atmosphere

Science.gov (United States)

Abo, M.; Shibata, Y.; Nagasawa, C.

2017-12-01

We have developed a ground based direct detection three-wavelength 1.6 μm differential absorption lidar (DIAL) to achieve measurements of vertical CO2 concentration and temperature profiles in the atmosphere. As the spectra of absorption lines of any molecules are influenced basically by the temperature and pressure in the atmosphere, it is important to measure them simultaneously so that the better accuracy of the DIAL measurement is realized. Conventionally, we have obtained the vertical profile of absorption cross sections using the atmospheric temperature profile by the objective analysis and the atmospheric pressure profile calculated by the pressure height equation. Comparison of atmospheric pressure profiles calculated from this equation and those obtained from radiosonde observations at Tateno, Japan is consistent within 0.2 % below 3 km altitude. But the temperature dependency of the CO2 density is 0.25 %/°C near the surface. Moreover, the CO2 concentration is often evaluated by the mixing ratio. Because the air density is related by the ideal gas law, the mixing ratio is also related by the atmospheric temperature. Therefore, the temperature affects not only accuracy of CO2 concentration but the CO2 mixing ratio. In this paper, some experimental results of the simultaneous measurement of atmospheric temperature profiles and CO2 mixing ratio profiles are reported from 0.4 to 2.5 km altitude using the three-wavelength 1.6 μm DIAL system. Temperature profiles of CO2 DIAL measurement were sometimes different from those of objective analysis below 1.5 km altitude. These differences are considered to be due to regionality at the lidar site. The temperature difference of 5.0 °C corresponds to a CO2 mixing ratio difference of 8.0 ppm at 500 m altitude. This cannot be ignored in estimates of regional sources and sinks of CO2. This three-wavelength CO2 DIAL technique can estimate accurately temporal behavior of CO2 mixing ratio profiles in the lower atmosphere

Highly Surface-Active Ca(OH)2 Monolayer as a CO2 Capture Material.

Science.gov (United States)

Özçelik, V Ongun; Gong, Kai; White, Claire E

2018-03-14

Greenhouse gas emissions originating from fossil fuel combustion contribute significantly to global warming, and therefore the design of novel materials that efficiently capture CO 2 can play a crucial role in solving this challenge. Here, we show that reducing the dimensionality of bulk crystalline portlandite results in a stable monolayer material, named portlandene, that is highly effective at capturing CO 2 . On the basis of theoretical analysis comprised of ab initio quantum mechanical calculations and force-field molecular dynamics simulations, we show that this single-layer phase is robust and maintains its stability even at high temperatures. The chemical activity of portlandene is seen to further increase upon defect engineering of its surface using vacancy sites. Defect-containing portlandene is capable of separating CO and CO 2 from a syngas (CO/CO 2 /H 2 ) stream, yet is inert to water vapor. This selective behavior and the associated mechanisms have been elucidated by examining the electronic structure, local charge distribution, and bonding orbitals of portlandene. Additionally, unlike conventional CO 2 capturing technologies, the regeneration process of portlandene does not require high temperature heat treatment because it can release the captured CO 2 by application of a mild external electric field, making portlandene an ideal CO 2 capturing material for both pre- and postcombustion processes.

Extracorporeal CO2 removal: Technical and physiological fundaments and principal indications.

Science.gov (United States)

Romay, E; Ferrer, R

2016-01-01

In recent years, technological improvements have reduced the complexity of extracorporeal membrane oxygenation devices. This have enabled the development of specific devices for the extracorporeal removal of CO2. These devices have a simpler configuration than extracorporeal membrane oxygenation devices and uses lower blood flows which could reduce the potential complications. Experimental studies have demonstrated the feasibility, efficacy and safety of extracorporeal removal of CO2 and some of its effects in humans. This technique was initially conceived as an adjunct therapy in patients with severe acute respiratory distress syndrome, as a tool to optimize protective ventilation. More recently, the use of this technique has allowed the emergence of a relatively new concept called "tra-protective ventilation"whose effects are still to be determined. In addition, the extracorporeal removal of CO2 has been used in patients with exacerbated hypercapnic respiratory failure with promising results. In this review we will describe the physiological and technical fundamentals of this therapy and its variants as well as an overview of the available clinical evidence, focused on its current potential. Copyright © 2015 Elsevier España, S.L.U. and SEMICYUC. All rights reserved.

Leaf shape responds to temperature but not CO2 in Acer rubrum.

Science.gov (United States)

Royer, Dana L

2012-01-01

The degree of leaf dissection and the presence of leaf teeth, along with tooth size and abundance, inversely correlate with mean annual temperature (MAT) across many plant communities. These relationships form the core of several methods for reconstructing MAT from fossils, yet the direct selection of temperature on tooth morphology has not been demonstrated experimentally. It is also not known if atmospheric CO(2) concentration affects leaf shape, limiting confidence in ancient climate reconstructions because CO(2) has varied widely on geologic timescales. Here I report the results of growing Acer rubrum (red maple) in growth cabinets at contrasting temperature and CO(2) conditions. The CO(2) treatment imparted no significant differences in leaf size and shape, while plants grown at cooler temperatures tended to have more teeth and more highly dissected leaves. These results provide direct evidence for the selection of temperature on leaf shape in one species, and support a key link in many leaf-climate methods. More broadly, these results increase confidence for using leaf shape in fossils to reconstruct paleoclimate.

Dynamic ikaite production and dissolution in sea ice - control by temperature, salinity and pCO2 conditions

Science.gov (United States)

Rysgaard, S.; Wang, F.; Galley, R. J.; Grimm, R.; Lemes, M.; Geilfus, N.-X.; Chaulk, A.; Hare, A. A.; Crabeck, O.; Else, B. G. T.; Campbell, K.; Papakyriakou, T.; Sørensen, L. L.; Sievers, J.; Notz, D.

2013-12-01

Ikaite is a hydrous calcium carbonate mineral (CaCO3 · 6H2O). It is only found in a metastable state, and decomposes rapidly once removed from near-freezing water. Recently, ikaite crystals have been found in sea ice and it has been suggested that their precipitation may play an important role in air-sea CO2 exchange in ice-covered seas. Little is known, however, of the spatial and temporal dynamics of ikaite in sea ice. Here we present evidence for highly dynamic ikaite precipitation and dissolution in sea ice grown at an out-door pool of the Sea-ice Environmental Research Facility (SERF). During the experiment, ikaite precipitated in sea ice with temperatures below -3 °C, creating three distinct zones of ikaite concentrations: (1) a mm to cm thin surface layer containing frost flowers and brine skim with bulk concentrations of > 2000 μmol kg-1, (2) an internal layer with concentrations of 200-400 μmol kg-1 and (3) a~bottom layer with concentrations of ikaite crystals under acidic conditions. Manual removal of the snow cover allowed the sea ice to cool and brine salinities to increase, resulting in rapid ikaite precipitation. The modeled (FREZCHEM) ikaite concentrations were in the same order of magnitude as observations and suggest that ikaite concentration in sea ice increase with decreasing temperatures. Thus, varying snow conditions may play a key role in ikaite precipitation and dissolution in sea ice. This will have implications for CO2 exchange with the atmosphere and ocean.

Effect of Chromium on Corrosion Behavior of P110 Steels in CO2-H2S Environment with High Pressure and High Temperature

Directory of Open Access Journals (Sweden)

Jianbo Sun

2016-03-01

Full Text Available The novel Cr-containing low alloy steels have exhibited good corrosion resistance in CO2 environment, mainly owing to the formation of Cr-enriched corrosion film. In order to evaluate whether it is applicable to the CO2 and H2S coexistence conditions, the corrosion behavior of low-chromium steels in CO2-H2S environment with high pressure and high temperature was investigated using weight loss measurement and surface characterization. The results showed that P110 steel suffered localized corrosion and both 3Cr-P110 and 5Cr-P110 steels exhibited general corrosion. However, the corrosion rate of 5Cr-P110 was the highest among them. The corrosion process of the steels was simultaneously governed by CO2 and H2S. The outer scales on the three steels mainly consisted of FeS1−x crystals, whereas the inner scales on Cr-containing steels comprised of amorphous FeS1−x, Cr(OH3 and FeCO3, in contrast with the amorphous FeS1−x and FeCO3 mixture film of P110 steel. The more chromium the steel contains, the more chromium compounds the corrosion products contain. The addition of chromium in steels increases the uniformity of the Cr-enriched corrosion scales, eliminates the localized corrosion, but cannot decrease the general corrosion rates. The formation of FeS1−x may interfere with Cr-enriched corrosion scales and lowering the corrosion performance of 3Cr-P110 and 5Cr-P110 steels.

Effect of Chromium on Corrosion Behavior of P110 Steels in CO2-H2S Environment with High Pressure and High Temperature

Science.gov (United States)

Sun, Jianbo; Sun, Chong; Lin, Xueqiang; Cheng, Xiangkun; Liu, Huifeng

2016-01-01

The novel Cr-containing low alloy steels have exhibited good corrosion resistance in CO2 environment, mainly owing to the formation of Cr-enriched corrosion film. In order to evaluate whether it is applicable to the CO2 and H2S coexistence conditions, the corrosion behavior of low-chromium steels in CO2-H2S environment with high pressure and high temperature was investigated using weight loss measurement and surface characterization. The results showed that P110 steel suffered localized corrosion and both 3Cr-P110 and 5Cr-P110 steels exhibited general corrosion. However, the corrosion rate of 5Cr-P110 was the highest among them. The corrosion process of the steels was simultaneously governed by CO2 and H2S. The outer scales on the three steels mainly consisted of FeS1−x crystals, whereas the inner scales on Cr-containing steels comprised of amorphous FeS1−x, Cr(OH)3 and FeCO3, in contrast with the amorphous FeS1−x and FeCO3 mixture film of P110 steel. The more chromium the steel contains, the more chromium compounds the corrosion products contain. The addition of chromium in steels increases the uniformity of the Cr-enriched corrosion scales, eliminates the localized corrosion, but cannot decrease the general corrosion rates. The formation of FeS1−x may interfere with Cr-enriched corrosion scales and lowering the corrosion performance of 3Cr-P110 and 5Cr-P110 steels. PMID:28773328

High-temperature electrolysis of CO2-enriched mixtures by using fuel-electrode supported La0.6Sr0.4CoO3/YSZ/Ni-YSZ solid oxide cells

Science.gov (United States)

Kim, Si-Won; Bae, Yonggyun; Yoon, Kyung Joong; Lee, Jong-Ho; Lee, Jong-Heun; Hong, Jongsup

2018-02-01

To mitigate CO2 emissions, its reduction by high-temperature electrolysis using solid oxide cells is extensively investigated, for which excessive steam supply is assumed. However, such condition may degrade its feasibility due to massive energy required for generating hot steam, implying the needs for lowering steam demand. In this study, high-temperature electrolysis of CO2-enriched mixtures by using fuel-electrode supported La0.6Sr0.4CoO3/YSZ/Ni-YSZ solid oxide cells is considered to satisfy such needs. The effect of internal and external steam supply on its electrochemical performance and gas productivity is elucidated. It is shown that the steam produced in-situ inside the fuel-electrode by a reverse water gas shift reaction may decrease significantly the electrochemical resistance of dry CO2-fed operations, attributed to self-sustaining positive thermo-electrochemical reaction loop. This mechanism is conspicuous at low current density, whereas it is no longer effective at high current density in which total reactant concentrations for electrolysis is critical. To overcome such limitations, a small amount of external steam supply to the CO2-enriched feed stream may be needed, but this lowers the CO2 conversion and CO/H2 selectivity. Based on these results, it is discussed that there can be minimum steam supply sufficient for guaranteeing both low electrochemical resistance and high gas productivity.

Study of the effect of pressure on electrolysis of H2O and co-electrolysis of H2O and CO2 at high temperature

International Nuclear Information System (INIS)

Bernadet, Lucile

2016-01-01

This thesis work investigates the behavior of a solid oxide cell operating under pressure in high temperature steam electrolysis and co-electrolysis mode (H 2 O and CO 2 ). The experimental study of single cell associated with the development of multi-physical models have been set up. The experiments, carried out using an original test bench developed by the CEA-Grenoble on two types of cells between 1 and 10 bar and 700 to 800 C, allowed to identify in both operating modes that the pressure has a positive or negative effect on performance depending on the cell operating point (current, voltage). In addition, gas analyzes performed in co-electrolysis led to detect in situ CH 4 production under pressure. These pressure effects were simulated by models calibrated at atmospheric pressure. Simulations analysis helped identify the pressure dependent mechanisms and propose operating conditions thanks to the establishment of operating maps. (author) [fr

High temperature oxidation and electrochemical studies on novel co-base superalloys

Energy Technology Data Exchange (ETDEWEB)

Klein, Leonhard

2013-02-27

Isothermal oxidation in air was carried out on novel γ'-strengthened Cobalt-base superalloys of the system Co-Al-W-B. After fast initial oxide formation, a multi-layered structure establishes, consisting of an outer cobalt oxide layer, a middle spinel-containing layer, and an inner Al{sub 2}O{sub 3}-rich region. Ion diffusion in outward direction is hindered by the development of Al{sub 2}O{sub 3}, that can be either present as a continuous and protective layer or as a discontinuous Al{sub 2}O{sub 3}-rich area without comparable protective effect. Furthermore, high temperature oxidation leads to phase transformation (from γ/γ' into γ/Co{sub 3}W) at the alloy/oxide layer interface due to aluminium depletion. Pure cobalt and ternary Co-Al-W alloys exhibit parabolic oxide growth due to the lack or insufficient amounts of protective oxides, whereas quaternary Co-Al-W-B alloys possess sub-parabolic oxidation behaviour (at 900 C). At lower temperatures (800 C), even a blockage of further oxidation can be observed. High amounts of B (0.12 at%) significantly improve oxidation resistance mainly due to its beneficial effect on inner Al{sub 2}O{sub 3}-formation at the alloy/oxide interface. Furthermore, B prevents decohesion of high temperature scales due to the formation of B-rich phases (presumably tungsten borides) in the middle oxide layer. Appropriate amounts of chromium (8 at%) as additional alloying element to Co-Al-W-B alloys lead to the formation of an inner duplex layer composed of protective Cr{sub 2}O{sub 3} and Al{sub 2}O{sub 3} phases. In this respect, chromium also benefits selective oxidation of aluminium, which results in higher Al{sub 2}O{sub 3}-contents compared to chromium-free alloys. Major drawbacks of chromium additions are, on the one hand, the formation of volatile chromium-containing species at temperatures exceeding 1000 C and on the other hand, the instability of the γ/γ'-microstructure. Titanium and silicon additions lead to

Simultaneous studies on solar energy storage by CO2 reduction to HCOOH with Brilliant Green dye removal photoelectrochemically

Directory of Open Access Journals (Sweden)

V.S.K. Yadav

2016-12-01

Full Text Available The simultaneous study on photoelectrochemical CO2 reduction with Brilliant Green (BG dye removal was studied in the present work. Experimental studies were done in aqueous solutions of sodium and potassium based electrolytes using a cathode [Zinc (Zn and Tin (Sn] and a common cobalt oxide (Co3O4 anode electrocatalyst. The influence of reaction with electrolyte concentration for the both catalysts was shown clearly with respect to time. The selected electrocatalysts were able to reduce CO2 to formic acid (HCOOH along with high BG dye removal. With Sn as cathode, the maximum BG dye removal was obtained to be KHCO3–[95.9% (10 min–0.2 M], NaHCO3–[98.6% (15 min–0.6 M]. Similarly for Zn, KHCO3–[99.8% (10 min–0.4 M], NaHCO3–[99.9% (20 min–0.8 M] were observed respectively. Finally, the results have proven that higher efficiencies for BG dye removal were obtained along with HCOOH formation, which might be a better alternate for water purification and to decrease the atmospheric CO2 concentrations.

A novel highly efficient adsorbent {[Co4(L)2(μ3-OH)2(H2O)3(4,4‧-bipy)2]·(H2O)2}n: Synthesis, crystal structure, magnetic and arsenic (V) absorption capacity

Science.gov (United States)

Zhang, Chong; Xiao, Yu; Qin, Yan; Sun, Quanchun; Zhang, Shuhua

2018-05-01

A novel highly efficient adsorbent-microporous tetranuclear Co(II)-based polymer, {[Co4(L)2(μ3-OH)2(H2O)3(4,4‧-bipy)2]·(H2O)2}n (1, H3L = 4-(N,N‧-bis(4-carboxybenzyl)amino) benzenesulfonic acid, 4,4‧-bipy = 4,4‧-bipyridine), was hydrothermally synthesized. The complex 1 is a metal-organic framework (MOF) material which was characterized by single-crystal X-ray diffraction, BET and platon software. Co-MOF (complex 1) reveals excellent adsorption property. The capacity of Co-MOF to remove arsenic As(V) from sodium arsenate aqueous solutions was investigated (The form of As(V) is AsO43-). The experimental results showed that Co-MOF had a higher stable and relatively high As(V) removal rate (> 98%) at pH 4-10. The adsorption kinetics followed a pseudo-second-order kinetic model, and the adsorption isotherm followed the Langmuir equation. Co-MOF exhibits a very high adsorption capacity of As(V) in aqueous solution (Qmax of 96.08 mg/g). Finally, the optimal adsorption conditions for the model were obtained through a Box-Behnken response surface experiment which was designed with adsorption time, dose, temperature and rotational speed of the shaker as the influencing factors to determine two-factor interaction effects. Co-MOF was further characterized using FTIR, PXRD, X-ray photoelectron spectroscopy before and after adsorption As (V). The magnetism of Co-MOF was also discussed.

Impact of CO2 injection protocol on fluid-solid reactivity: high-pressure and temperature microfluidic experiments in limestone

Science.gov (United States)

Jimenez-Martinez, Joaquin; Porter, Mark; Carey, James; Guthrie, George; Viswanathan, Hari

2017-04-01

Geological sequestration of CO2 has been proposed in the last decades as a technology to reduce greenhouse gas emissions to the atmosphere and mitigate the global climate change. However, some questions such as the impact of the protocol of CO2 injection on the fluid-solid reactivity remain open. In our experiments, two different protocols of injection are compared at the same conditions (8.4 MPa and 45 C, and constant flow rate 0.06 ml/min): i) single phase injection, i.e., CO2-saturated brine; and ii) simultaneous injection of CO2-saturated brine and scCO2. For that purpose, we combine a unique high-pressure/temperature microfluidics experimental system, which allows reproducing geological reservoir conditions in geo-material substrates (i.e., limestone, Cisco Formation, Texas, US) and high resolution optical profilometry. Single and multiphase flow through etched fracture networks were optically recorded with a microscope, while processes of dissolution-precipitation in the etched channels were quantified by comparison of the initial and final topology of the limestone micromodels. Changes in hydraulic conductivity were quantified from pressure difference along the micromodel. The simultaneous injection of CO2-saturated brine and scCO2, reduced the brine-limestone contact area and also created a highly heterogeneous velocity field (i.e., low velocities regions or stagnation zones, and high velocity regions or preferential paths), reducing rock dissolution and enhancing calcite precipitation. The results illustrate the contrasting effects of single and multiphase flow on chemical reactivity and suggest that multiphase flow by isolating parts of the flow system can enhance CO2 mineralization.

REMOVAL OF H(sub 2)S AND SO(sub 2) BY CaCO(sub 3)-BASED SORBENTS AT HIGH PRESSURES; SEMIANNUAL

International Nuclear Information System (INIS)

Prof. Stratis V. Sotirchos

1999-01-01

The effects of various operating and process parameters on the direct sulfidation of limestones, that is, their reaction with H(sub 2)S in the presence of CO(sub 2) at concentrations large enough to prevent the decomposition of CaCO(sub 3) to CaO. Two calcitic solids of high calcium carbonate content (over 97%) were employed in the experiments, and the reaction was studied in a thermogravimetric analysis system that can operate at pressures above atmospheric. Pressures in the 1-4 atm range were employed. The results showed that the pressure influenced the behavior of the process mainly through its effects on the concentration of H(sub 2)S, and the rate of the reaction was found to be of first order with respect to this variable. The behavior of the process could be described satisfactorily by a shrinking core model with a product layer diffusivity that depended only on the temperature and did not vary with the distance from the external surface of the particles. The results on the effects of particle size, temperature, limestone sample, and concentration of H(sub 2)S were in agreement with those in a past investigation of the direct sulfidation reaction of limestones in our laboratory at atmospheric pressure. For the next six-month period, we plan to conduct experiments on the effects of the effects of carbonation reaction on the sulfation of calcined limestones. As explained in the introductory section of this report, this situation may occur as calcined particles move into areas of the combustor where the concentration of CO(sub 2) is above the equilibrium value for the calcination reaction at the prevailing temperature

High temperature infrared absorption cross sections of methane near 3.4 μm in Ar and CO2 mixtures

Science.gov (United States)

Koroglu, Batikan; Neupane, Sneha; Pryor, Owen; Peale, Robert E.; Vasu, Subith S.

2018-02-01

The absorption cross-sections of CH4 at two wavelengths in the mid-IR region: λpeak = 3403.4 nm and λvalley = 3403.7 nm were measured. Data were taken using three different compositions of non-reactive gas mixtures comprising CH4/Ar/CO2 between 700 laser. Also, broadband room temperature methane cross section measurements were performed using a Fourier transform infrared spectrometer and the cascade laser to gain a better insight into the changes of the line shapes in various bath gasses (Ar, CO2, and N2). An application of the high-temperature cross-section data was demonstrated to determine the concentration of methane during oxy-methane combustion in a mixture of CO2, O2, and Ar. Current measurements will be valuable addition to the spectroscopy database for methane- an important fuel used for power generation and heating around the world.

High power CO2 lasers and their applications in nuclear industry

International Nuclear Information System (INIS)

Nath, A.K.

2002-01-01

Carbon dioxide laser is one of the most popular lasers in industry for material processing applications. It has very high power capability and high efficiency, can be operated in continuous wave (CW), modulated and pulsed modes, and has relatively low cost. Due to these characteristics high power CO 2 lasers are being used worldwide in different industries for a wide variety of materials processing operations. In nuclear industry, CO 2 laser has made its way in many applications. Some of the tasks performed by multikilowatt CO 2 laser are cutting operations necessary to remove unprocessible hardware from reactor fuel assemblies, sealing/fixing/removing radioactive contaminations onto/from concrete surfaces and surface modification of engineering components for improved surface mechanical and metallurgical characteristics. We have developed various models of CW CO 2 lasers of power up to 12 kW and a high repetitive rate TEA (Transversely Excited Atmospheric pressure) CO 2 laser of 500 W average power operating at 500 Hz repetition rates. We have carried many materials processing applications of direct relevance to DAE. Recent work includes laser welding of end plug PFBR fuel tubes, martensitic stainless steel and titanium alloy, surface cladding of turbine blades made of Ni-super alloy with stellite 694, fabrication on graded material of stainless steel and stellite, and laser scabbling, drilling and cutting of concrete which have potential application in decontamination and decommissioning of nuclear facilities. A brief overview of these indigenous developments will be presented. (author)

Bioelectrochemical removal of carbon dioxide (CO2): an innovative method for biogas upgrading.

Science.gov (United States)

Xu, Heng; Wang, Kaijun; Holmes, Dawn E

2014-12-01

Innovative methods for biogas upgrading based on biological/in-situ concepts have started to arouse considerable interest. Bioelectrochemical removal of CO2 for biogas upgrading was proposed here and demonstrated in both batch and continuous experiments. The in-situ biogas upgrading system seemed to perform better than the ex-situ one, but CO2 content was kept below 10% in both systems. The in-situ system's performance was further enhanced under continuous operation. Hydrogenotrophic methanogenesis and alkali production with CO2 absorption could be major contributors to biogas upgrading. Molecular studies showed that all the biocathodes associated with biogas upgrading were dominated by sequences most similar to the same hydrogenotrophic methanogen species, Methanobacterium petrolearium (97-99% sequence identity). Conclusively, bioelectrochemical removal of CO2 showed great potential for biogas upgrading. Copyright © 2014 Elsevier Ltd. All rights reserved.

Influence of O{sub 2} on the dielectric properties of CO{sub 2} at the elevated temperatures

Energy Technology Data Exchange (ETDEWEB)

Rong, Mingzhe; Sun, Hao; Yang, Fei, E-mail: yfei2007@mail.xjtu.edu.cn; Wu, Yi, E-mail: wuyic51@mail.xjtu.edu.cn; Chen, Zhexin; Wang, Xiaohua; Wu, Mingliang [State Key Laboratory of Electrical Insulation and Power Equipment, Xi' an Jiaotong University, Xi' an Shaanxi 710049 (China)

2014-11-15

SF{sub 6} gas is widely used in the high voltage circuit breakers but considering its high global warming potential other substitutes are being sought. Among them CO{sub 2} was investigated and even has been used in some practical products. However, at room temperature, the dielectric properties of CO{sub 2} are relatively lower than SF{sub 6} and air. The goal of this work is to investigate a CO{sub 2}-based gas to improve the performance of the pure CO{sub 2}. In this paper, the dielectric properties of hot CO{sub 2}/O{sub 2} mixtures related to the dielectric recovery phase of the circuit breaker were investigated in the temperature range from 300 K to 4000 K and in the pressure range from 0.01 MPa to 1.0 MPa. The species compositions of hot CO{sub 2}/O{sub 2} were obtained based on Gibbs free energy minimization under the assumptions of local thermodynamic equilibrium and local chemical equilibrium. The reduced critical electric field strength of CO{sub 2}/O{sub 2} was determined by balancing electron generation and loss. These were calculated using the electron energy distribution function by solving the Boltzmann transport equation. The validity of the calculation method and the cross sections data was confirmed by comparing the measurements and calculations of the electron swarm data in previous work. The results indicate that in pure CO{sub 2} the critical electric field strength is higher only in higher temperature range. By adding the O{sub 2} into the CO{sub 2}, the critical electric field strength at lower temperature is effectively enhanced. CO{sub 2}/O{sub 2} mixtures have a much better dielectric strength than both the pure CO{sub 2} and air and thus have the potential to improve the CO{sub 2}-based gas circuit breakers. Similar conclusions can also be found in others’ work, which further confirm the validity of these results.

Room-temperature ionic liquids and composite materials: platform technologies for CO(2) capture.

Science.gov (United States)

Bara, Jason E; Camper, Dean E; Gin, Douglas L; Noble, Richard D

2010-01-19

Clean energy production has become one of the most prominent global issues of the early 21st century, prompting social, economic, and scientific debates regarding energy usage, energy sources, and sustainable energy strategies. The reduction of greenhouse gas emissions, specifically carbon dioxide (CO(2)), figures prominently in the discussions on the future of global energy policy. Billions of tons of annual CO(2) emissions are the direct result of fossil fuel combustion to generate electricity. Producing clean energy from abundant sources such as coal will require a massive infrastructure and highly efficient capture technologies to curb CO(2) emissions. Current technologies for CO(2) removal from other gases, such as those used in natural gas sweetening, are also capable of capturing CO(2) from power plant emissions. Aqueous amine processes are found in the vast majority of natural gas sweetening operations in the United States. However, conventional aqueous amine processes are highly energy intensive; their implementation for postcombustion CO(2) capture from power plant emissions would drastically cut plant output and efficiency. Membranes, another technology used in natural gas sweetening, have been proposed as an alternative mechanism for CO(2) capture from flue gas. Although membranes offer a potentially less energy-intensive approach, their development and industrial implementation lags far behind that of amine processes. Thus, to minimize the impact of postcombustion CO(2) capture on the economics of energy production, advances are needed in both of these areas. In this Account, we review our recent research devoted to absorptive processes and membranes. Specifically, we have explored the use of room-temperature ionic liquids (RTILs) in absorptive and membrane technologies for CO(2) capture. RTILs present a highly versatile and tunable platform for the development of new processes and materials aimed at the capture of CO(2) from power plant flue gas and

Performance Estimation of Supercritical CO2 Cycle for the PG-SFR application with Heat Sink Temperature Variation

International Nuclear Information System (INIS)

Ahn, Yoonhan; Cho, Seong Kuk; Lee, Jeong Ik

2015-01-01

The heat sink temperature conditions are referred from the annual database of sea water temperature in East sea. When the heat sink temperature increases, the compressor inlet temperature can be influenced and the sudden power decrease can happen due to the large water pumping power. When designing the water pump, the pumping margin should be considered as well. As a part of Prototype Generation IV Sodium-cooled Fast Reactor (PG-SFR) development, the Supercritical CO 2 cycle (S-CO 2 ) is considered as one of the promising candidate that can potentially replace the steam Rankine cycle. S-CO 2 cycle can achieve distinctively high efficiency compared to other Brayton cycles and even competitive performance to the steam Rankine cycle under the mild turbine inlet temperature region. Previous studies explored the optimum size of the S-CO 2 cycle considering component designs including turbomachinery, heat exchangers and pipes. Based on the preliminary design, the thermal efficiency is 31.5% when CO 2 is sufficiently cooled to the design temperature. However, the S-CO 2 compressor performance is highly influenced by the inlet temperature and the compressor inlet temperature can be changed when the heat sink temperature, in this case sea water temperature varies. To estimate the S-CO 2 cycle performance of PG-SFR in the various regions, a Quasi-static system analysis code for S-CO 2 cycle is developed by the KAIST research team. A S-CO 2 cycle for PG-SFR is designed and assessed for off-design performance with the heat sink temperature variation

The microbial community in a high-temperature enhanced biological phosphorus removal (EBPR process

Directory of Open Access Journals (Sweden)

Ying Hui Ong

2016-01-01

Full Text Available An enhanced biological phosphorus removal (EBPR process operated at a relatively high temperature, 28 °C, removed 85% carbon and 99% phosphorus from wastewater over a period of two years. This study investigated its microbial community through fluorescent in situ hybridization (FISH and clone library generation. Through FISH, considerably more Candidatus “Accumulibacter phosphatis” (Accumulibacter-polyphosphate accumulating organisms (PAOs than Candidatus ‘Competibacter phosphatis’ (Competibacter-glycogen accumulating organisms were detected in the reactor, at 36 and 7% of total bacterial population, respectively. A low ratio of Glycogen/Volatile Fatty Acid of 0.69 further indicated the dominance of PAOs in the reactor. From clone library generated, 26 operational taxonomy units were retrieved from the sludge and a diverse population was shown, comprising Proteobacteria (69.6%, Actinobacteria (13.7%, Bacteroidetes (9.8%, Firmicutes (2.94%, Planctomycetes (1.96%, and Acidobacteria (1.47%. Accumulibacter are the only recognized PAOs revealed by the clone library. Both the clone library and FISH results strongly suggest that Accumulibacter are the major PAOs responsible for the phosphorus removal in this long-term EBPR at relatively high temperature.

Research and survey report of FY 1997 on the CO2 balance for high-temperature CO2 fixation and utilization technology; 1997 nendo chosa hokokusho (nisanka tanso koon bunri gijutsu ni okeru CO2 balance ni kansuru chosa kenkyu)

Energy Technology Data Exchange (ETDEWEB)

NONE

1998-03-01

The purpose of this research is to clarify the application condition and effectiveness of high-temperature CO2 fixation and utilization technology. To evaluate the present process, it was compared with others, such as separation using a polymer membrane, physico-chemical absorption process, adsorption process, hydrogen contact reduction process, and biological fixation. The development trends of absorption, membrane, adsorption, and cryogenic separation were investigated. The questionnaire was carried out about the separation technologies which are in the stage of performance test using actual gas, to arrange and compare the data and information. The current trends of chemical and biological CO2 fixation and utilization technology were also investigated for arranging the subjects. High-temperature CO2 disposal by the carbonation in concrete waste has been studied, to clarify its application conditions and effectiveness. In order to compare the separation technologies, treatment processes of CO2 in the exhaust gas from boilers of LNG power generation and coal fired power generation were simulated. These processes were simulated by ASPEN PLUS for the modeling. Trends of application of ASPEN PLUS and collection of information were surveyed by participating in the ASPEN WORLD. 103 refs., 51 figs., 55 tabs.

Removal of 14C-contaminated CO2 from simulated LWR fuel reprocessing off-gas by utilizing the reaction between CO2 and alkaline hydroxides in either slurry or solid form

International Nuclear Information System (INIS)

Holladay, D.W.; Haag, G.L.

1979-01-01

An important consideration in the design of a LWR fuel reprocessing plant is the removal of 14 C-contaminated CO 2 from the process off-gas. The separation and fixation of essentially all the CO 2 from the simulated off-gas can be accomplished by reaction with alkaline slurries in agitated tank-type contactors. Based on efficacy for CO 2 removal, consideration of reactant cost, and stability of the carbonate product as related to long-term storage requirements, the two most promising slurry reactants for CO 2 removal from low CO 2 -content feed gases are Ca(OH) 2 and Ba(OH) 2 . The removal of 14 C-contaminated CO 2 from simulated LWR off-gases was studied as a function of both operating conditions and varying sizes of bench-scale design. Parametrically, the effects on the CO 2 removal rate of feed composition (330 ppM - 4.47% CO 2 ), impeller speed (325 to 650 rpm), superficial velocity (5 to 80 cm/min), reactants [Mg(OH) 2 , NaOH], contactor size (20.3 cm and 27.3 cm ID), and type of operation (semibatch or continuous slurry) were deterined

Passive Decay Heat Removal System Options for S-CO2 Cooled Micro Modular Reactor

International Nuclear Information System (INIS)

Moon, Jangsik; Jeong, Yong Hoon; Lee, Jeong Ik

2014-01-01

To achieve modularization of whole reactor system, Micro Modular Reactor (MMR) which has been being developed in KAIST took S-CO 2 Brayton power cycle. The S-CO 2 power cycle is suitable for SMR due to high cycle efficiency, simple layout, small turbine and small heat exchanger. These characteristics of S-CO 2 power cycle enable modular reactor system and make reduced system size. The reduced size and modular system motived MMR to have mobility by large trailer. Due to minimized on-site construction by modular system, MMR can be deployed in any electricity demand, even in isolated area. To achieve the objective, fully passive safety systems of MMR were designed to have high reliability when any offsite power is unavailable. In this research, the basic concept about MMR and Passive Decay Heat Removal (PDHR) system options for MMR are presented. LOCA, LOFA, LOHS and SBO are considered as DBAs of MMR. To cope with the DBAs, passive decay heat removal system is designed. Water cooled PDHR system shows simple layout, but has CCF with reactor systems and cannot cover all DBAs. On the other hand, air cooled PDHR system with two-phase closed thermosyphon shows high reliability due to minimized CCF and is able to cope with all DBAs. Therefore, the PDHR system of MMR will follows the air-cooled PDHR system and the air cooled system will be explored

Temperature study of magnetic resonance spectra of co-modified (Co,N-TiO2 nanocomposites

Directory of Open Access Journals (Sweden)

Guskos Nikos

2016-06-01

Full Text Available The (nCo,N-TiO2 (n = 1, 5 and 10 wt.% of Co nanocomposites were investigated by magnetic resonance spectroscopy in 4 K to 290 K range. Analyses of ferromagnetic/electron paramagnetic resonance (FMR/EPR spectra in terms of four Callen lineshape components revealed the existence of two types of magnetic centers, one derived from metallic cobalt nanoparticles in superparamagnetic (SPM phase and the other from cobalt clusters in the TiO2 lattice. Additionally, at low temperature the EPR spectrum arising from Ti3+ ions was also registered. Both relaxations of the Landau-Lifshitz type and the Bloch-Bloembergen type played an important role at high temperature in determining the linewidths and the latter relaxation was prevailing at low temperature. Analysis of the integrated intensity showed that the SPM signal is due to small size FM cobalt nanoparticles while the paramagnetic signal from Co clusters originates from those nanoparticles in which the concentration of magnetic polarons is below the percolation threshold.

Note: A dual temperature closed loop batch reactor for determining the partitioning of trace gases within CO2-water systems.

Science.gov (United States)

Warr, Oliver; Rochelle, Christopher A; Masters, Andrew J; Ballentine, Christopher J

2016-01-01

An experimental approach is presented which can be used to determine partitioning of trace gases within CO2-water systems. The key advantages of this system are (1) The system can be isolated with no external exchange, making it ideal for experiments with conservative tracers. (2) Both phases can be sampled concurrently to give an accurate composition at each phase at any given time. (3) Use of a lower temperature flow loop outside of the reactor removes contamination and facilitates sampling. (4) Rapid equilibration at given pressure/temperature conditions is significantly aided by stirring and circulating the water phase using a magnetic stirrer and high-pressure liquid chromatography pump, respectively.

Study on the conversion of H2 and CO from the helium carrier gas of high temperature gas-cooled reactor

International Nuclear Information System (INIS)

Liao Cuiping; Zheng Zhenhong; Shi Fuen

1995-01-01

The conversions of hydrogen and carbon monoxide into water vapor and carbon dioxide on CuO-ZnO-Al 2 O 3 catalyst are studied. The effects of different temperature, system atmospheric pressure, impurity gas concentration, flow and dew point on properties of cupric oxide bed are investigated. The conversion characteristics curves of H 2 and CO are given. Experimental data of conversion capacity, action period and conversion efficiency of CuO-ZnO-Al 2 O 3 are obtained and the optimal parameters are determined. The results show that the concentration of H 2 and CO of the effluent gas after purification can reach below 2 x 10 -6 , respectively. So it can meet the demands of high temperature gas-cooled reactor and also provide optimal design parameters and reliable data for conversion of H 2 and CO on CuO-ZnO-Al 2 O 3 catalyst

Seawater bicarbonate removal during hydrothermal circulation

Science.gov (United States)

Proskurowski, G. K.; Seewald, J.; Sylva, S. P.; Reeves, E.; Lilley, M. D.

2013-12-01

High temperature fluids sampled at hydrothermal vents represent a complex alteration product of water-rock reactions on a multi-component mixture of source fluids. Sources to high-temperature hydrothermal samples include the 'original' seawater present in the recharge limb of circulation, magmatically influenced fluids added at depth as well as any seawater entrained during sampling. High-temperature hydrothermal fluids are typically enriched in magmatic volatiles, with CO2 the dominant species, characterized by concentrations of 10's-100's of mmol/kg (1, 2). Typically, the high concentration of CO2 relative to background seawater bicarbonate concentrations (~2.3 mmol/kg) obscures a full analysis of the fate of seawater bicarbonate during high-temperature hydrothermal circulation. Here we present data from a suite of samples collected over the past 15 years from high-temperature hydrothermal vents at 9N, Endeavour, Lau Basin, and the MAR that have endmember CO2 concentrations less than 10 mmol/kg. Using stable and radiocarbon isotope measurements these samples provide a unique opportunity to examine the balance between 'original' seawater bicarbonate and CO2 added from magmatic sources. Multiple lines of evidence from multiple hydrothermal settings consistently points to the removal of ~80% of the 'original' 2.3 mmol/kg seawater bicarbonate. Assuming that this removal occurs in the low-temperature, 'recharge' limb of hydrothermal circulation, this removal process is widely occurring and has important contributions to the global carbon cycle over geologic time. 1. Lilley MD, Butterfield DA, Lupton JE, & Olson EJ (2003) Magmatic events can produce rapid changes in hydrothermal vent chemistry. Nature 422(6934):878-881. 2. Seewald J, Cruse A, & Saccocia P (2003) Aqueous volatiles in hydrothermal fluids from the Main Endeavour Field, northern Juan de Fuca Ridge: temporal variability following earthquake activity. Earth and Planetary Science Letters 216(4):575-590.

Tightened constraints on the time-lag between Antarctic temperature and CO2 during the last deglaciation

Directory of Open Access Journals (Sweden)

T. D. van Ommen

2012-07-01

Full Text Available Antarctic ice cores provide clear evidence of a close coupling between variations in Antarctic temperature and the atmospheric concentration of CO2 during the glacial/interglacial cycles of at least the past 800-thousand years. Precise information on the relative timing of the temperature and CO2 changes can assist in refining our understanding of the physical processes involved in this coupling. Here, we focus on the last deglaciation, 19 000 to 11 000 yr before present, during which CO2 concentrations increased by ~80 parts per million by volume and Antarctic temperature increased by ~10 °C. Utilising a recently developed proxy for regional Antarctic temperature, derived from five near-coastal ice cores and two ice core CO2 records with high dating precision, we show that the increase in CO2 likely lagged the increase in regional Antarctic temperature by less than 400 yr and that even a short lead of CO2 over temperature cannot be excluded. This result, consistent for both CO2 records, implies a faster coupling between temperature and CO2 than previous estimates, which had permitted up to millennial-scale lags.

The effect of Co-firing with Straw and Coal on High Temperature Corrosion

DEFF Research Database (Denmark)

Montgomery, Melanie; Frandsen, Flemming; Larsen, OH

2001-01-01

As a part of ELSAMS development programme into alternative energy sources, various concepts of straw-firing have been investigated. This paper concerns co-firing of straw with coal to reduce the corrosion rate observed in straw-fired power plants. Co-firing with coal reduces the amount of potassium......: a) the exposure of metal rings on water/air cooled probes, and b) the exposure of a range of materials built into the existing superheaters. A range of austenitic and ferritic steels was exposed in the steam temperature region of 520-580°C. The flue gas temperature ranged from 925-1100°C....... The corrosion products for the various steel types were investigated using light optical and scanning electron microscopy. Corrosion mechanisms for the austenitic and ferritic steels are presented. These are discussed in relation to temperature and deposit composition. Co-firing with coal has removed potassium...

High-temperature plastic flow of a precipitation-hardened FeCoNiCr high entropy alloy

Energy Technology Data Exchange (ETDEWEB)

He, J.Y.; Wang, H.; Wu, Y.; Liu, X.J. [State Key Laboratory for Advanced Metals and Materials, University of Science and Technology Beijing, Beijing 100083 (China); Nieh, T.G. [Department of Materials Science and Engineering, the University of Tennessee, Knoxville, TN 37996 (United States); Lu, Z.P., E-mail: luzhaoping@163.com [State Key Laboratory for Advanced Metals and Materials, University of Science and Technology Beijing, Beijing 100083 (China)

2017-02-16

In this work, we systematically investigated flow behavior of a high entropy alloy (HEA) strengthened by coherent γ′ precipitates in the temperature range of 1023–1173 K. In contrast to the single-phase FeCoNiCrMn HEA, this precipitate-hardened alloy, i.e., (FeCoNiCr){sub 94}Ti{sub 2}Al{sub 4}, exhibited large reduction of the steady-state strain rate (by ~2 orders of magnitude) or drastic enhancement in flow stress, indicating significant improvement in high-temperature properties. Our results showed that the deformation could be divided into two regimes. At temperatures below 1123 K, coherent γ′ precipitates effectively blocked the dislocation motion, thus resulted in a threshold stress effect. Above 1123 K, however, γ′ particles dissolved and the deformation was controlled by the ordinary dislocation climb mechanism. In addition, we conducted transmission electron microscopy to characterize dislocation-precipitate interaction to provide microstructural evidences to support our conclusion of the specific deformation mechanisms in the two temperature regimes.

High speed surface cleaning by a high repetition rated TEA-CO2 laser

International Nuclear Information System (INIS)

Tsunemi, Akira; Hirai, Ryo; Hagiwara, Kouji; Nagasaka, Keigo; Tashiro, Hideo

1994-01-01

We demonstrated the feasibility of high speed cleaning of solid surfaces by the laser ablation technique using a TEA-CO 2 laser. The laser pulses with the repetition rate of 1 kHz were applied to paint, rust, moss and dirt attached on the surfaces. The attachments were effectively removed without the damage of bulk surfaces by the irradiation of line-focused sequential pulses with an energy of 300 mJ/pulse. A cleaning rate reached to 17 m 2 /hour for the case of paint removal from iron surfaces. (author)

Syngas production by gasification of aquatic biomass with CO2/O2 and simultaneous removal of H2S and COS using char obtained in the gasification

International Nuclear Information System (INIS)

Hanaoka, Toshiaki; Hiasa, Shou; Edashige, Yusuke

2013-01-01

Applicability of gulfweed as feedstock for a biomass-to-liquid (BTL) process was studied for both production of gas with high syngas (CO + H 2 ) content via gasification of gulfweed and removal of gaseous impurities using char obtained in the gasification. Gulfweed as aqueous biomass was gasified with He/CO 2 /O 2 using a downdraft fixed-bed gasifier at ambient pressure and 900 °C at equivalence ratios (ER) of 0.1–0.3. The syngas content increased while the conversion to gas on a carbon basis decreased with decreasing ER. At an ER of 0.1 and He/CO 2 /O 2 = 0/85/15%, the syngas content was maximized at 67.6% and conversion to gas on a carbon basis was 94.2%. The behavior of the desulfurization using char obtained during the gasification process at ER = 0.1 and He/CO 2 /O 2 = 0/85/15% was investigated using a downdraft fixed-bed reactor at 250–550 °C under 3 atmospheres (H 2 S/N 2 , COS/N 2 , and a mixture of gases composed of CO, CO 2 , H 2 , N 2 , CH 4 , H 2 S, COS, and steam). The char had a higher COS removal capacity at 350 °C than commercial activated carbon because (Ca,Mg)S crystals were formed during desulfurization. The char simultaneously removed H 2 S and COS from the mixture of gases at 450 °C more efficiently than did activated carbon. These results support this novel BTL process consisting of gasification of gulfweed with CO 2 /O 2 and dry gas cleaning using self-supplied bed material. -- Highlights: • A product gas with high syngas content was produced from the gasification of gulfweed with CO 2 /O 2 . • The syngas content increased with decreasing the equivalence ratio. • The syngas content was maximized at 67.6% at an ER of 0.1 and He/CO 2 /O 2 = 0/85/15%. • The char simultaneously removed H 2 S and COS from a mixture of gases at 450 °C efficiently

The effect of elevated CO2 and temperature on nutrient uptake by plants grown in basaltic soil

Science.gov (United States)

Villasenor Iribe, E.; Dontsova, K.; Juarez, S.; Le Galliard, J. F.; Chollet, S.; Llavata, M.; Massol, F.; Barré, P.; Gelabert, A.; Daval, D.; Troch, P.; Barron-Gafford, G.; Van Haren, J. L. M.; Ferrière, R.

2017-12-01

Mineral weathering is an important process in soil formation. The interactions between the hydrologic, geologic and atmospheric cycles often determine the rate at which weathering occurs. Elements and nutrients weathered from the soil by water can be removed from soils in the runoff and seepage, but they can also remain in situ as newly precipitated secondary minerals or in biomass as a result of plant uptake. Here we present data from an experiment that was conducted at the controlled environment facility, Ecotron Ile-de-France (Saint-Pierre-les-Nemours, France) that studied mineral weathering and plant growth in granular basaltic material with high glass content that is being used to simulate soil in large scale Biosphere 2 Landscape Evolution Observatory (LEO) project. The experiment used 3 plant types: velvet mesquite (Prosopis velutina), green spangletop (Leptochloa dubia), and alfalfa (Medicago sativa), which were grown under varying temperature and CO2 conditions. We hypothesized that plants grown under warmer, higher CO2 conditions would have larger nutrient concentrations as more mineral weathering would occur. Results of plant digestions and analysis showed that plant concentrations of lithogenic elements were significantly influenced by the plant type and were different between above- and below-ground parts of the plant. Temperature and CO2 treatment effects were less pronounced, but we observed significant temperature effect on plant uptake. A number of major and trace elements showed increase in concentration with increase in temperature at elevated atmospheric CO2. Effect was observed both in the shoots and in the roots, but more significant differences were observed in the shoots. Results presented here indicate that climate change would have strong effect on plant uptake and mobility of weathered elements during soil formation and give further evidence of interactions between abiotic and biological processes in terrestrial ecosystems.

Potential high temperature corrosion problems due to co-firing of biomass and fossil fuels

DEFF Research Database (Denmark)

Montgomery, Melanie; Vilhelmsen, T.; Jensen, S.A.

2008-01-01

Over the past few years, considerable high temperature corrosion problems have been encountered when firing biomass in power plants due to the high content of potassium chloride in the deposits. Therefore, to combat chloride corrosion problems cofiring of biomass with a fossil fuel has been...... undertaken. This results in potassium chloride being converted to potassium sulphate in the combustion chamber and it is sulphate rich deposits that are deposited on the vulnerable metallic surfaces such as high temperature superheaters. Although this removes the problem of chloride corrosion, other...... corrosion mechanisms appear such as sulphidation and hot corrosion due to sulphate deposits. At Studstrup power plant Unit 4, based on trials with exposure times of 3000 h using 0–20% straw co-firing with coal, the plant now runs with a fuel mix of 10% strawþcoal. Based on results from a 3 years exposure...

Photocatalytic oxidation removal of Hg{sup 0} using ternary Ag/AgI-Ag{sub 2}CO{sub 3} hybrids in wet scrubbing process under fluorescent light

Energy Technology Data Exchange (ETDEWEB)

Zhang, Anchao, E-mail: aczhang@qq.com [School of Mechanical and Power Engineering, Henan Polytechnic University, Jiaozuo, 454000 (China); Zhang, Lixiang; Chen, Xiaozhuan; Zhu, Qifeng; Liu, Zhichao [School of Mechanical and Power Engineering, Henan Polytechnic University, Jiaozuo, 454000 (China); Xiang, Jun, E-mail: xiangjun@mail.hust.edu.cn [State Key Laboratory of Coal Combustion, Huazhong University of Science and Technology, Wuhan, 430074 (China)

2017-01-15

Highlights: • Ag/AgI-Ag{sub 2}CO{sub 3} hybrids were employed for Hg{sup 0} removal under fluorescent light. • Superoxide radical (·O{sub 2}{sup −}) played a key role in Hg{sup 0} removal. • NO exhibited a significant effect on Hg{sup 0} removal in comparison to SO{sub 2}. • The mechanism for enhanced Hg{sup 0} removal over Ag/AgI-Ag{sub 2}CO{sub 3} was proposed. - Abstract: A series of ternary Ag/AgI-Ag{sub 2}CO{sub 3} photocatalysts synthesized using a facile coprecipitation method were employed to investigate their performances of Hg{sup 0} removal in a wet scrubbing reactor. The hybrids were characterized by N{sub 2} adsorption-desorption, XRD, SEM-EDS, HRTEM, XPS, DRS and ESR. The photocatalytic activities of Hg{sup 0} removal were evaluated under fluorescent light. The results showed that AgI content, fluorescent light irradiation, reaction temperature all showed significant influences on Hg{sup 0} removal. NO exhibited significant effect on Hg{sup 0} removal in comparison to SO{sub 2}. Among these ternary Ag/AgI-Ag{sub 2}CO{sub 3} hybrids, Ag/AgI(0.1)-Ag{sub 2}CO{sub 3} showed the highest Hg{sup 0} removal efficiency, which could be ascribed to the effective separation of photogenerated electron-hole pairs between AgI and Ag{sub 2}CO{sub 3} and the surface plasmon resonance (SPR) effect in the visible region by metallic silver nanoparticles (Ag{sup 0} NPs). The trapping studies of reactive radicals showed that the superoxide radicals (·O{sub 2}{sup −}) may play a key role in Hg{sup 0} removal under fluorescent light. According to the experimental and characterization results, a possible photocatalytic oxidation mechanism for enhanced Hg{sup 0} removal over Ag/AgI(0.1)-Ag{sub 2}CO{sub 3} hybrid under fluorescent light was proposed.

An investigation of sodium–CO{sub 2} interaction byproduct cleaning agent for SFR coupled with S-CO{sub 2} Brayton cycle

Energy Technology Data Exchange (ETDEWEB)

Jung, Hwa-Young, E-mail: jhy0523@kaist.ac.kr [Department of Nuclear and Quantum Engineering, Korea Advanced Institute of Science and Technology, 373-1 Guseong-dong Yuseong-gu, Daejeon 305-701 (Korea, Republic of); Division of SFR NSSS System Design, Korea Atomic Energy Research Institute, 111, Daedeok-daero 989beon-gil, Yuseong-gu, Daejeon 305-353 (Korea, Republic of); Lee, Jeong Ik, E-mail: jeongiklee@kaist.ac.kr [Department of Nuclear and Quantum Engineering, Korea Advanced Institute of Science and Technology, 373-1 Guseong-dong Yuseong-gu, Daejeon 305-701 (Korea, Republic of); Wi, Myung-Hwan, E-mail: mhwi@kaeri.re.kr [Division of SFR NSSS System Design, Korea Atomic Energy Research Institute, 111, Daedeok-daero 989beon-gil, Yuseong-gu, Daejeon 305-353 (Korea, Republic of); Ahn, Hong Joo, E-mail: ahjoo@kaeri.re.kr [Division of Nuclear Chemistry Research, Korea Atomic Energy Research Institute, 111, Daedeok-daero 989beon-gil, Yuseong-gu, Daejeon 305-353 (Korea, Republic of)

2016-02-15

Highlights: • Study on cleaning agent was conducted to remove Na–CO{sub 2} interaction byproducts. • Screening criteria to select candidate substances as cleaning agents were suggested. • The mixtures of Na{sub 2}CO{sub 3} with NaBrO{sub 3}, NaClO{sub 3}, or NaBF{sub 4} were thermally analyzed with the TG/DTA studies. • Three candidate substances decomposed before 600 °C and did not react with Na{sub 2}CO{sub 3}. - Abstract: One of the promising future nuclear energy systems, the Sodium-cooled Fast Reactor (SFR) has been actively developed internationally. Recently, to improve safety and economics of a SFR further, coupling supercritical CO{sub 2} power cycle was suggested. However, there can be a chemical reaction between sodium and CO{sub 2} at high temperature (more than 400 °C) when the pressure boundary fails in a sodium–CO{sub 2} heat exchanger. To ensure the performance of such a system, it is important to employ a cleaning agent to recover the system back to normal condition after the reaction. When sodium and CO{sub 2} react, solid and gaseous reaction products such as sodium carbonate (Na{sub 2}CO{sub 3}) and carbon monoxide (CO) appear. Since most of solid reaction products are hard and can deteriorate system performance, quick removal of solid reaction products becomes very important for economic performance of the system. Thus, the authors propose the conceptual method to remove the byproducts with a chemical reaction at high temperature. The chemical reaction will take place between the reaction byproducts and a cleaning agent while the cleaning agent is inert with sodium. Thus, various sodium-based compounds were first investigated and three candidate substances satisfying several criteria were selected; sodium bromate (NaBrO{sub 3}), sodium chlorate (NaClO{sub 3}), and sodium tetrafluoroborate (NaBF{sub 4}). The selected substances were thermally analyzed with the TG/DTA studies. Unfortunately, it was revealed that all candidate

Effect of Temperature on the Kinetics of Sorption of Co2+ and Ni2+ Ions by a Sorbent Based on an Inositol Hexaphosphoric Acid Derivative

Science.gov (United States)

Yarusova, S. B.; Makarenko, N. V.; Gordienko, P. S.; Karpenko, M. A.; Novikova, E. S.

2018-03-01

Data on the effect temperature has on the kinetics of the removal of Co2+ and Ni2+ ions under static conditions by a sorbent based on a derivative of phytic acid fabricated from rice production waste are presented. It is shown that when the temperature is raised from 20 to 60°C, the sorption capacity of the sorbent based on phytic acid increases over the period of sorption and within 180 min reaches values of 1.4 mmol g-1 for Co2+ ions and 1.3 mmol g-1 for Ni2+ ions. It is established that for the investigated range of temperatures, order n of the sorption of Co2+ and Ni2+ ions is frame is best described by a kinetic model of a pseudo-second order, as is indicated by respective correlation coefficients.

Light availability and temperature, not increased CO2, will structure future meadows of Posidonia oceanica

KAUST Repository

Hendriks, Iris E.; Olsen, Ylva S.; Duarte, Carlos M.

2017-01-01

We evaluated the photosynthetic performance of Posidonia oceanica during short-term laboratory exposures to ambient and elevated temperatures (24–25°C and 29–30°C) warming and pCO2 (380, 750 and 1000ppm pCO2) under normal and low light conditions (200 and 40μmol photons m−2s−1 respectively). Plant growth was measured at the low light regime and showed a negative response to warming. Light was a critical factor for photosynthetic performance, although we found no evidence of compensation of photosynthetic quantum efficiency in high light. Relative Electron Rate Transport (rETRmax) was higher in plants incubated in high light, but not affected by pCO2 or temperature. The saturation irradiance (Ik) was negatively affected by temperature. We conclude that elevated CO2 does not enhance photosynthetic activity and growth, in the short term for P. oceanica, while temperature has a direct negative effect on growth. Low light availability also negatively affected photosynthetic performance during the short experimental period examined here. Therefore increasing concentrations of CO2 may not compensate for predicted future conditions of warmer water and higher turbidity for seagrass meadows.

Light availability and temperature, not increased CO2, will structure future meadows of Posidonia oceanica

KAUST Repository

Hendriks, Iris E.

2017-02-15

We evaluated the photosynthetic performance of Posidonia oceanica during short-term laboratory exposures to ambient and elevated temperatures (24–25°C and 29–30°C) warming and pCO2 (380, 750 and 1000ppm pCO2) under normal and low light conditions (200 and 40μmol photons m−2s−1 respectively). Plant growth was measured at the low light regime and showed a negative response to warming. Light was a critical factor for photosynthetic performance, although we found no evidence of compensation of photosynthetic quantum efficiency in high light. Relative Electron Rate Transport (rETRmax) was higher in plants incubated in high light, but not affected by pCO2 or temperature. The saturation irradiance (Ik) was negatively affected by temperature. We conclude that elevated CO2 does not enhance photosynthetic activity and growth, in the short term for P. oceanica, while temperature has a direct negative effect on growth. Low light availability also negatively affected photosynthetic performance during the short experimental period examined here. Therefore increasing concentrations of CO2 may not compensate for predicted future conditions of warmer water and higher turbidity for seagrass meadows.

Selective removal of Cs and Re by precipitation in a Na2CO3-H2O2 solution

International Nuclear Information System (INIS)

Eil-Hee Lee; Jae-Gwan Lim; Dong-Yong Chung; Han-Beom Yang; Kwang-Wook Kim

2010-01-01

The removal of Cs and Re (as a surrogate for Tc) by selective precipitation from the simulated fission products which were co-dissolved with uranium during the oxidative dissolution of spent fuel in a Na 2 CO 3 -H 2 O 2 solution was investigated in this study. The precipitations of Cs and Re were examined by introducing sodium tetraphenylborate (NaTPB) and tetraphenylohosponium chloride (TPPCl), respectively. The precipitation of Cs by NaTPB and that of Re by TPPCl each took place within 5 min, and an increase in temperature up to 50 deg C and a stirring speed up to 1000 rpm hardly affected their precipitation rates. The most important factor in the precipitation with NaTPB and TPPCl was found to be a pH of the solution after precipitation. Since Mo tends to co-precipitate with Cs or Re at a lower pH, an effective precipitation with NaTPB and TPPCl was done at pH of above 9 without the co-precipitation of Mo. More than 99% of Cs and Re were precipitated when the initial concentration ratio of NaTPB to Cs was above 1 and when that of TPPCl to Re was above 1. The precipitation of Cs and Re was never affected by the concentration of Na 2 CO 3 and H 2 O 2 , even though they were raised up to 1.5 and 1.0 M, respectively. Precipitation yields of Cs and Re in a Na 2 CO 3 -H 2 O 2 solution were found to be dependent on the concentration ratios of [NaTBP]/[Cs] and [TPPCl]/[Re]. (author)

Application of dual membrane contactor for simultaneous CO2 removal using continues diethanolamine (DEA)

Science.gov (United States)

Rahmawati, Yeni; Nurkhamidah, Siti; Susianto, Listiyana, Nidia Intan; Putricahyani, Widyawati

2017-05-01

Technology of membrane contactor is an improvemet of acid gas (CO2) removal technology that combining gas absorption process with solvent and membrane technology. The objective of the experiment are study the effect of feed gas flow rate and solvent to flux CO2 and efficiency of CO2 removal, and also study the performance of membrane contactor. The experiment is conducted by circulating DEA in certain flow rate and arranging hollow fiber membrane in double-crossed section with the amount of desorption membrane three times more than absorption membrane. Feed gas streamed in the tube of membrane absorption and solvent on the shell. At the same time and condition, the process of desorption is done by streamed N2 gas as the stripping gas in desorption membrane. Performance test is conducted by running optimum variable for 8 hours. The result showed that flux of absorption gain the highest at 24,747 × 10-4 mol/m2.s, while flux of desorption gain the highest at 1,761 × 10-4 mol/m2.s. Increasing of absorption flux correspond to increasing of flow rate of feed gas and CO2 gas concentration but decreasing in flow rate of solvent. Increasing of desorption flux correspond to increasing of flow rate of feed gas and solvent but concentration of CO2 does not have impact. Efficiency increase while flow rate of mix gas and solvent decreasing, but CO2 concentration increase. The highest efficiency is 61,64%. Efficiency performance for CO2 removal of module membrane has the highest value at first 2 hours and stay constant at next running for 8 hours.

CO2 capture from air by Chlorella vulgaris microalgae in an airlift photobioreactor.

Science.gov (United States)

Sadeghizadeh, Aziz; Farhad Dad, Farid; Moghaddasi, Leila; Rahimi, Rahbar

2017-11-01

In this work, hydrodynamics and CO 2 biofixation study was conducted in an airlift bioreactor at the temperature of 30±2°C. The main objective of this work was to investigate the effect of high gas superficial velocity on CO 2 biofixation using Chlorella vulgaris microalgae and its growth. The study showed that Chlorella vulgaris in high input gas superficial velocity also had the ability to grow and remove the CO 2 by less than 80% efficiency. Copyright © 2017 Elsevier Ltd. All rights reserved.

Photosynthetic pigments and gas exchange in castor bean under conditions of above the optimal temperature and high CO2

Directory of Open Access Journals (Sweden)

Fabiola França Silva

2015-08-01

Full Text Available The castor bean plant, a Euphorbiaceae oil seed C3-metabolism rustic and drought-resistant plant, is cultivated in a wide range of environments due to its good adaptive capacity. However, given the current environmental changes, many biochemical and physiological impacts may affect the productivity of important crops, such as castor bean. This work aimed to evaluate the impacts of the castor bean gas exchange in response to high temperature and increased CO2concentration.Our experiment was conducted in a phytotron located at Embrapa Algodão in 2010. We adopted a completely randomized design, with four treatments in a factorial combination of two temperatures (30/20 and 37/30°C and two CO2 levels (400 and 800 mmol L-1; four replications were performed, obtained in five surveys over the growth cycle, for a total of 80 sample units. An infrared gas analyzer (IRGA - Infra Red Gas Analyzer was used for the quantification of the photosynthetic rate, stomatal conductance and transpiration. An increase in the atmospheric CO2 concentration and temperature negatively affected the physiology of the castor bean plants, decreasing the net rate of photosynthesis, transpiration and stomatal conductance.

Photosynthetic response to variation in CO2 concentrations and temperature of four broad-leaved trees in Beijing region

Institute of Scientific and Technical Information of China (English)

Zhibo MA; Shengqing SHI; Qinyan MA; Yutao WANG; Xingliang LIU

2008-01-01

Responses of the photosynthetic characteris-tics to variation in CO2 concentration and temperature of Ginkgo biloba, Eucornmia ulmoides, Magnolia denudata and Tiliajaponica were measured during the peak growing season. The results show that the ambient CO2 concentra-tion could not meet the requirements for photosynthesis of these four species. The optimal temperatures for pho-tosynthesis were lower than the average daytime air tem-perature. Hence, the photosynthesis of these four species was restricted by the low CO2 concentration and high daytime air temperature at the time of measurement. Marked enhancements in the net photosynthetic rate were found in all four species when the CO2 concentration was doubled. When the dependency on CO2 and temperature were examined simultaneously, it was seen that for increased CO2 concentrations there was a shift in the optimum temperature for M. denudata and T. japonica towards higher temperatures. Due to their independence on CO2 concentrations, this trend could not be found in the G. biloba and E. ulmoides data sets. The stomatal con-ductance (Gs) was sensitive to a vapor pressure deficit (VPD) which in turn was sensitive to temperature. An increase in temperature would cause the VPD to increase and plants might be assumed to react by reducing their stomatal apertures. The effect on stomatal resistance would be most significant at high temperatures. The restriction to stomatal conductance for these four species would increase if CO2 concentrations were elevated at the same temperature.

Elevated tropospheric CO2 and O3 concentrations impair organic pollutant removal from grassland soil.

Science.gov (United States)

Ai, Fuxun; Eisenhauer, Nico; Jousset, Alexandre; Butenschoen, Olaf; Ji, Rong; Guo, Hongyan

2018-04-03

The concentrations of tropospheric CO 2 and O 3 have been rising due to human activities. These rising concentrations may have strong impacts on soil functions as changes in plant physiology may lead to altered plant-soil interactions. Here, the effects of eCO 2 and eO 3 on the removal of polycyclic aromatic hydrocarbon (PAH) pollutants in grassland soil were studied. Both elevated CO 2 and O 3 concentrations decreased PAH removal with lowest removal rates at elevated CO 2 and elevated O 3 concentrations. This effect was linked to a shift in soil microbial community structure by structural equation modeling. Elevated CO 2 and O 3 concentrations reduced the abundance of gram-positive bacteria, which were tightly linked to soil enzyme production and PAH degradation. Although plant diversity did not buffer CO 2 and O 3 effects, certain soil microbial communities and functions were affected by plant communities, indicating the potential for longer-term phytoremediation approaches. Results of this study show that elevated CO 2 and O 3 concentrations may compromise the ability of soils to degrade organic pollutants. On the other hand, the present study also indicates that the targeted assembly of plant communities may be a promising tool to shape soil microbial communities for the degradation of organic pollutants in a changing world.

Effects of CO2 and temperature on growth and resource use of co-occurring C3 and C4 annuals

International Nuclear Information System (INIS)

Coleman, J.S.; Bazzaz, F.A.

1992-01-01

The authors examined how CO 2 concentrations and temperature interacted to affect growth, resource acquisition, and resource allocation of two annual plants that were supplied with a single pulse of nutrients. Physiological and growth measurements were made on individuals of Abutilon throphrasti (C 3 ) and Amaranthus retroflexus (C 4 ) grown in environments with atmospheric CO 2 levels of 400 or 700 μL/L and with light/dark temperatures of 28 degree/22 degree or 38 degree/31 degree C. Elevated CO 2 and temperature treatments had significant independent and interactive effects on plant growth, resource allocation, and resource acquisition, and the strength and direction of these effects were often dependent on plant species. For example, final biomass of Amaranthus was enhanced by elevated CO 2 at 28 degree but was depressed at 38 degree. For Abutilon, elevated CO 2 increased initial plant relative growth rates at 28 degree but not at 38 degree, and had no significant effects on final biomass at either temperature. These results are interpreted in light of the interactive effects of CO 2 and temperature on the rates of net leaf area production and loss, and on net whole-plant nitrogen retention. At 28 degree C, elevated CO 2 stimulated the initial production of leaf area in both species, which led to an initial stimulation of biomass accumulation at the higher CO 2 level. However, in elevated CO 2 at 28 degree, the rate of net leaf area loss for Abutilon increased while that of Amaranthus decreased. Furthermore, high CO 2 apparently enhanced the ability of Amaranthus to retain nitrogen at this temperature, which may have helped to enhance photosynthesis, whereas nitrogen retention was unaffected in Abutilon

High temperature reactor: Driving force to convert CO2 to fuel - HTR2008-58132

International Nuclear Information System (INIS)

McCormick, J. L.

2008-01-01

The rapidly increasing cost of petroleum products and uncertainty of long-term supply have prompted the U.S. military to aggressively pursue production of alternative fuels (synfuels) such as coal-to-liquids (CTL). U.S. Air Force is particularly active in this effort while the entire military is involved in simultaneously developing fuel specifications for alternative fuels that enable a single fuel for the entire battle space; all ground vehicles, aircraft and fuel cells. By limiting its focus on coal, tar sands and oil shale resources, the military risks violating federal law which requires the use of synfuels that have life cycle greenhouse gas emissions less than or equal to emissions from conventional petroleum fuels. A climate-friendly option would use a high temperature nuclear reactor to split water. The hydrogen (H 2 ) would be used in the reverse water gas shift (RWGS) to react with carbon dioxide (CO 2 ) to produce carbon monoxide (CO) and water. The oxygen (O 2 ) would be fed into a supercritical (SC) coal furnace. The flue gas CO 2 emissions would be stripped of impurities before reacting with H 2 in a RWGS process. Resultant carbon monoxide (CO) is fed, with additional H2, (extra H 2 needed to adjust the stoichiometry: 2 moles H 2 to one mole CO) into a conventional Fischer-Tropsch synthesis (FTS) to produce a heavy wax which is cracked and isomerized and refined to Jet Propulsion 8 (JP-8) and Jet Propulsion 5 (JP-5) fuels. The entire process offers valuable carbon-offsets and multiple products that contribute to lower syn-fuel costs and to comply with the federal limitation imposed on syn-fuel purchases. While the entire process is not commercially available, component parts are being researched; their physical and chemical properties understood and some are state-of-the-art technologies. An international consortium should complete physical, chemical and economic flow sheets to determine the feasibility of this concept that, if pursued, has broad

Absorption of CO2 laser light by a dense, high temperature plasma

International Nuclear Information System (INIS)

Peacock, N.J.; Forrest, M.J.; Morgan, P.D.; Offenberger, A.A.

1977-01-01

The interaction between a pulsed, CO 2 laser beam and the plasma produced in a plasma focus device is investigated theoretically and experimentally. The CO 2 laser radiation, directed orthogonal to the pinch axis and along the density gradient only weakly perturbs the focus since the radiation density of 30 J cm -3 (allowing for the Airy enhancement factor near the critical layer), is still less than the plasma thermal energy >=1 kJ cm -3 . On the contrary, the CO 2 laser beam is grossly affected by the plasma and absorption during the compressed pinch phase when the plasma frequency is much more complete than can be predicted by classical resistivity. Density fluctuations at the Langmuir frequency are measured directly for forward scattering from a probe, ruby laser beam. Since the wave numbers correspond to approximately 0.1 the Langmuir waves should appear as electron 'lines' in the scattered spectrum shifted by 427 A from the ruby laser wavelength. At low CO 2 laser pump intensity the electron wave intensity is close to the thermal level. As the pump is increased beyond a threshold of approximately 3x10 9 W/cm -2 (in vacuo) enhanced scattering is observed, reaching a factor of 30 above thermal. A WKB treatment of the electron-ion decay instability which takes into account the linear growth of waves at equal electron and ion temperatures and their convection in an inhomogeneous plasma is reasonably consistent with the observations

Concurrent removal of elemental mercury and SO2 from flue gas using a thiol-impregnated CaCO3-based adsorbent: a full factorial design study.

Science.gov (United States)

Balasundaram, Karthik; Sharma, Mukesh

2018-03-22

Mercury (Hg) emitted from coal-based thermal power plants (CTPPs) can accumulate and bio-magnify in the food chain, thereby posing a risk to humans and wildlife. The central idea of this study was to develop an adsorbent which can concurrently remove elemental mercury (Hg 0 ) and SO 2 emitted from coal-based thermal power plants (CTPPs) in a single unit operation. Specifically, a composite adsorbent of CaCO 3 impregnated with 2-mercaptobenimidazole (2-MBI) (referred to as modified calcium carbonate (MCC)) was developed. While 2-MBI having sulfur functional group could selectively adsorb Hg 0 , CaCO 3 could remove SO 2 . Performance of the adsorbent was evaluated in terms of (i) removal (%) of Hg 0 and SO 2 , (ii) adsorption mechanism, (iii) adsorption kinetics, and (iv) leaching potential of mercury from spent adsorbent. The adsorption studies were performed using a 2 2 full factorial design of experiments with 15 ppbV of Hg 0 and 600 ppmV of SO 2 . Two factors, (i) reaction temperature (80 and 120 °C; temperature range in flue gas) and (ii) mass of 2-MBI (10 and 15 wt%), were investigated for the removal of Hg 0 and SO 2 (as %). The maximum Hg 0 and SO 2 removal was 86 and 93%, respectively. The results of XPS characterization showed that chemisorption is the predominant mechanism of Hg 0 and SO 2 adsorption on MCC. The Hg 0 adsorption on MCC followed Elovich kinetic model which is also indicative of chemisorption on heterogeneous surface. The toxicity characteristic leaching procedure (TCLP) and synthetic precipitation leaching procedure (SPLP) leached mercury from the spent adsorbent were within the acceptable levels defined in these tests. The engineering significance of this study is that the 2-MBI-modified CaCO 3 -based adsorbent has potential for concurrent removal of Hg 0 and SO 2 in a single unit operation. With only minor process modifications, the newly developed adsorbent can replace CaCO 3 in the flue-gas desulfurization (FGD) system.

Removal of Co(II) from aqueous solution by using hydroxyapatite

International Nuclear Information System (INIS)

Yan Huang; Liang Chen; Hualin Wang

2012-01-01

Herein, hydroxyapatite (HAP) was prepared by aqueous precipitation technique and was characterized by using FT-IR and XRD to determine its chemical functional groups and micro-structure. The removal of cobalt from aqueous solution to HAP was studied by batch technique as a function of various environmental parameters such as contact time, pH, ionic strength, foreign ions, fulvic acid (FA), and temperature under ambient conditions. The results indicated that the sorption of Co(II) on HAP was strongly dependent on pH and ionic strength. The presence of FA enhanced the sorption of Co(II) on HAP at low pH, whereas reduced Co(II) sorption on HAP at high pH. The Langmuir, Freundlich and D-R models were used to simulate the sorption isotherms at three different temperatures of 303.15, 323.15 and 343.15 K. The thermodynamic parameters (ΔHdeg, ΔSdeg and ΔGdeg) calculated from the temperature dependent sorption isotherms indicated that the sorption process of Co(II) on HAP was spontaneous and endothermic. The sorption of Co(II) was dominated by outer-sphere surface complexation and ion exchange at low pH, whereas inner-sphere surface complexation or surface precipitation was the main sorption mechanism at high pH values. The results suggest that the HAP is a suitable material in the preconcentration and solidification of Co(II) from large volumes of aqueous solutions. (author)

Oxygen order-disorder phase transition in PrBaCo2O5.48 at high temperature

International Nuclear Information System (INIS)

Streule, S.; Podlesnyak, A.; Pomjakushina, E.; Conder, K.; Sheptyakov, D.; Medarde, M.; Mesot, J.

2006-01-01

We have investigated the PrBaCo 2 O 5.48 compound by means of neutron powder diffraction at temperatures 300K OD =776K, which we associate with an oxygen order-disorder transition: the well-known room temperature ordered crystal structure, in which slabs of CoO 6 octahedra and CoO 5 pyramids interleave (Pmmm symmetry) gets lost at temperatures T>T OD , resulting in a statistical distribution of octahedra and pyramids in the sample. The new phase can be described by the tetragonal P4/mmm space group. The transition is caused by displacement of apical oxygen ions and is an indication that ionic conductivity, which has been observed in 3D cobaltites, may also exist in layered cobaltites

All-epitaxial Co{sub 2}FeSi/Ge/Co{sub 2}FeSi trilayers fabricated by Sn-induced low-temperature epitaxy

Energy Technology Data Exchange (ETDEWEB)

Kawano, M.; Ikawa, M.; Arima, K.; Yamada, S.; Kanashima, T.; Hamaya, K., E-mail: hamaya@ee.es.osaka-u.ac.jp [Graduate School of Engineering Science, Osaka University, 1-3 Machikaneyama, Toyonaka 560-8531 (Japan)

2016-01-28

We demonstrate low-temperature growth of all-epitaxial Co{sub 2}FeSi/Ge/Co{sub 2}FeSi trilayer structures by developing Sn-induced surfactant-mediated molecular beam epitaxy (SMBE) of Ge on Co{sub 2}FeSi. Despite the growth of a semiconductor on a metal, we verify that the inserted Sn monolayers between Ge and Co{sub 2}FeSi enable to promote the 2D epitaxial growth of Ge up to 5 nm at a T{sub G} of 250 °C. An understanding of the mechanism of the Sn-induced SMBE leads to the achievement of all-epitaxial Co{sub 2}FeSi/Ge/Co{sub 2}FeSi trilayer structures with spin-valve-like magnetization reversals. This study will open a way for vertical-type and high-performance Ge-based spintronics devices.

Modeling Silicate Weathering for Elevated CO2 and Temperature

Science.gov (United States)

Bolton, E. W.

2016-12-01

A reactive transport model (RTM) is used to assess CO2 drawdown by silicate weathering over a wide range of temperature, pCO2, and infiltration rates for basalts and granites. Although RTM's have been used extensively to model weathering of basalts and granites for present-day conditions, we extend such modeling to higher CO2 that could have existed during the Archean and Proterozoic. We also consider a wide range of surface temperatures and infiltration rates. We consider several model basalt and granite compositions. We normally impose CO2 in equilibrium with the various atmospheric ranges modeled and CO2 is delivered to the weathering zone by aqueous transport. We also consider models with fixed CO2 (aq) throughout the weathering zone as could occur in soils with partial water saturation or with plant respiration, which can strongly influence pH and mineral dissolution rates. For the modeling, we use Kinflow: a model developed at Yale that includes mineral dissolution and precipitation under kinetic control, aqueous speciation, surface erosion, dynamic porosity, permeability, and mineral surface areas via sub-grid-scale grain models, and exchange of volatiles at the surface. Most of the modeling is done in 1D, but some comparisons to 2D domains with heterogeneous permeability are made. We find that when CO2 is fixed only at the surface, the pH tends toward higher values for basalts than granites, in large part due to the presence of more divalent than monovalent cations in the primary minerals, tending to decrease rates of mineral dissolution. Weathering rates increase (as expected) with increasing CO2 and temperature. This modeling is done with the support of the Virtual Planetary Laboratory.

Low coral cover in a high-CO2 world

Science.gov (United States)

Hoegh-Guldberg, Ove

2005-09-01

Coral reefs generally exist within a relatively narrow band of temperatures, light, and seawater aragonite saturation states. The growth of coral reefs is minimal or nonexistent outside this envelope. Climate change, through its effect on ocean temperature, has already had an impact on the world's coral reefs, with almost 30% of corals having disappeared since the beginning of the 1980s. Abnormally warm temperatures cause corals to bleach (lose their brown dinoflagellate symbionts) and, if elevated for long enough, to die. Increasing atmospheric CO2 is also potentially affecting coral reefs by lowering the aragonite saturation state of seawater, making carbonate ions less available for calcification. The synergistic interaction of elevated temperature and CO2 is likely to produce major changes to coral reefs over the next few decades and centuries. Known tolerances of corals to projected changes to sea temperatures indicate that corals are unlikely to remain abundant on reefs and could be rare by the middle of this century if the atmospheric CO2 concentration doubles or triples. The combination of changes to sea temperature and carbonate ion availability could trigger large-scale changes in the biodiversity and function of coral reefs. The ramifications of these changes for the hundred of millions of coral reef-dependent people and industries living in a high-CO2 world have yet to be properly defined. The weight of evidence suggests, however, that projected changes will cause major shifts in the prospects for industries and societies that depend on having healthy coral reefs along their coastlines.

High efficient removal of molybdenum from water by Fe{sub 2}(SO{sub 4}){sub 3}: Effects of pH and affecting factors in the presence of co-existing background constituents

Energy Technology Data Exchange (ETDEWEB)

Zhang, Xiang; Ma, Jun, E-mail: majunhit@126.com; Lu, Xixin; Huangfu, Xiaoliu; Zou, Jing

2015-12-30

Highlights: • Proposed high efficient Mo (VI) removal with Fe{sub 2}(SO{sub 4}){sub 3} coagulation-filtration. • Studied different effects of Fe{sub 2}(SO{sub 4}){sub 3} and FeCl{sub 3} due to different anionic portions. • Reported the adverse effect of calcium on the removal of Mo (VI). • Proposed factors affecting Mo (VI) removal: intercepted Fe and adsorption affinity. - Abstract: Comparatively investigated the different effects of Fe{sub 2}(SO{sub 4}){sub 3} coagulation-filtration and FeCl{sub 3} coagulation-filtration on the removal of Mo (VI). And the influence of calcium, sulfate, silicate, phosphate and humic acid (HA) were also studied. The following conclusions can be obtained: (1) compared with the case of FeCl{sub 3}, Fe{sub 2}(SO{sub 4}){sub 3} showed a higher Mo (VI) removal efficiency at pH 4.00–5.00, but an equal removal efficiency at pH 6.00–9.00. (2) The optimum Mo (VI) removal by Fe{sub 2}(SO{sub 4}){sub 3} was achieved at pH 5.00–6.00; (3) The presence of calcium can reduce the removal of Mo (VI) over the entire pH range in the present study; (4) The effect of co-existing background anions (including HA) was dominated by three factors: Firstly the influence of co-existing background anions on the content of Fe intercepted from water (intercepted Fe). Secondly the competition of co-existing anions with Mo (VI) for adsorption sites. Thirdly the influence of co-existing background anions on the Zeta potential of the iron flocs.

A breakthrough in flue gas cleanup, CO2 mitigation and H2S removal

Energy Technology Data Exchange (ETDEWEB)

Koch, Wolf; Wasas, James; Stenger, Raymond; Howell, Evan

2010-09-15

SWAPSOL Corp. is developing commercial processes around a newly discovered reaction that reduces H2S below detectable levels while reacting with CO2 to form water, sulfur and carsuls, a carbon-sulfur polymer. The Stenger-Wasas Process (SWAP) stands to simplify sulfur removal technology as it consumes CO2 in an exothermic reaction. The SWAP has applications in landfill, sour, flue and Claus tail gas cleanup and may replace Claus technology. Destruction of waste hydrocarbons provides a source of H2S. The primary reactions and variants have been independently verified and the chemical kinetics determined by a third party laboratory.

Estimation of characteristics on high temperature filtration system for particle removal in vitrification process

International Nuclear Information System (INIS)

Park, Seung Chul; Ryu, Bo Hyun; Park, Byoung Chul; Ryu, Chang Soo; Hwang, Tae Won; Ha, Jong Hyun

2003-01-01

High temperature filtration technology has been widely used in nuclear industry systems to remove particulate matter from air and gas streams. Air filters are defined as porous structures through which air is passed to separate out entrained particulate matter. Especially among of them, ceramic candle filters are suitable to gain efficient dust removal at high temperatures and achieve high collection efficiencies for (sub-)micron particles. The paper presents experimental results for their application in the pilot scale vitrification plant operations. Experimental results were transformed into design equations for (i) total pressure drop and the effect of face velocity; (ii) the prediction of the operating parameters

Multi-species time-history measurements during high-temperature acetone and 2-butanone pyrolysis

KAUST Repository

Lam, Kingyiu

2013-01-01

High-temperature acetone and 2-butanone pyrolysis studies were conducted behind reflected shock waves using five species time-history measurements (ketone, CO, CH3, CH4 and C2H4). Experimental conditions covered temperatures of 1100-1600 Kat 1.6 atm, for mixtures of 0.25-1.5% ketone in argon. During acetone pyrolysis, the CO concentration time-history was found to be strongly sensitive to the acetone dissociation rate constant κ1 (CH3COCH3 → CH3 + CH3CO), and this could be directly determined from the CO time-histories, yielding κ1(1.6 atm) = 2.46 × 1014 exp(-69.3 [kcal/mol]/RT) s-1 with an uncertainty of ±25%. This rate constant is in good agreement with previous shock tube studies from Sato and Hidaka (2000) [3] and Saxena et al. (2009) [4] (within 30%) at temperatures above 1450 K, but is at least three times faster than the evaluation from Sato and Hidaka at temperatures below 1250 K. Using this revised κ1 value with the recent mechanism of Pichon et al. (2009) [5], the simulated profiles during acetone pyrolysis show excellent agreement with all five species time-history measurements. Similarly, the overall 2-butanone decomposition rate constant κtot was inferred from measured 2-butanone time-histories, yielding κ tot(1.5 atm) = 6.08 × 1013 exp(-63.1 [kcal/mol]/RT) s -1 with an uncertainty of ±35%. This rate constant is approximately 30% faster than that proposed by Serinyel et al. (2010) [11] at 1119 K, and approximately 100% faster at 1412 K. Using the measured 2-butanone and CO time-histories and an O-atom balance analysis, a missing removal pathway for methyl ketene was identified. The rate constant for the decomposition of methyl ketene was assumed to be the same as the value for the ketene decomposition reaction. Using the revised κtot value and adding the methyl ketene decomposition reaction to the Serinyel et al. mechanism, the simulated profiles during 2-butanone pyrolysis show good agreement with the measurements for all five species. �

Interactive effect of temperature and CO2 increase in Arctic phytoplankton

Directory of Open Access Journals (Sweden)

Alexandra eCoello-Camba

2014-10-01

Full Text Available An experiment was performed in order to analyze the effects of the increase in water temperature and CO2 partial pressure expected for the end of this century in a present phytoplankton community inhabiting the Arctic Ocean. We analyzed both factors acting independently and together, to test possible interactions between them. The arctic planktonic community was incubated under 6 different treatments combining three experimental temperatures (1 ºC, 6 ºC and 10 ºC with two different CO2 levels of 380 ppm or 1000 ppm, at the UNIS installations in Longyearbyen (Svalbard, in summer 2010. Under warmer temperatures, a decrease in chlorophyll a concentration, biovolume and primary production was found, together with a shift in community structure towards a dominance of smaller cells (nano-sized. Effects of increased pCO2 were more modest, and although interactions were weak, our results suggest antagonistic interactive effects amongst increased temperature and CO2 levels, as elevated CO2 compensated partially the decrease in phytoplankton biomass induced by temperature in some groups. Interactions between the two stressors were generally weak, but elevated CO2 was observed to lead to a stepper decline in primary production with warming. Our results also suggest that future increases in water temperature and pCO2 would lead to a decrease in the community chl a concentration and biomass in the Arctic phytoplankton communities examined, leading to communities dominated by smaller nano-phytoplankton groups, with important consequences for the flow of carbon and food web dynamics.

Enhanced Intermediate-Temperature CO2 Splitting Using Nonstoichiometric Ceria and Ceria-Zirconia

KAUST Repository

Zhao, Zhenlong

2017-08-24

CO2 splitting via thermo-chemical or reactive redox has emerged as a novel and promising carbon-neutral energy solution. Its performance depends critically on the properties of the oxygen carriers (OC). Ceria is recognized as one of the most promising OC candidates, because of its fast chemistry, high ionic diffusivity, and large oxygen storage capacity. The fundamental surface ion-incorporation pathways, along with the role of surface defects and the adsorbates remains largely unknown. This study presents a detailed kinetics study of CO2 splitting using CeO2 and Ce0.5Zr0.5O2 (CZO) in the temperature range 600-900℃. Given our interest in fuel-assisted reduction, we limit our study to relatively lower temperatures to avoid excessive sintering and the need for high temperature heat. Compared to what has been reported previously, we observe higher splitting kinetics, resulting from the utilization of fine particles and well-controlled experiments which ensure a surface-limited-process. The peak rates with CZO are 85.9 μmole g–1s–1 at 900℃ and 61.2 μmole g–1s–1 at 700℃, and those of CeO2 are 70.6 μmole g–1s–1 and 28.9 μmole g–1s–1. Kinetics models are developed to describe the ion incorporation dynamics, with consideration of CO2 activation and the charge transfer reactions. CO2 activation energy is found to be – 120 kJ mole-1 for CZO, half of that for CeO2, while CO desorption energetics is analogous among the two samples with the value of ~160 kJ mole-1. The charge-transfer process is found to be the rate-limiting step for CO2 splitting. The evolution of CO32- with surface Ce3+ is examined based on the modeled kinetics. We show that the concentration of CO32- varies with Ce3+ in a linear-flattened-decay pattern, resulting from a mismatch between the kinetics of the two reactions. Our study provides new insights into the significant role of the surface defects and adsorbates in determining the splitting kinetics.

Separation of Co{sup 2+} present in aqueous solution on calcium carbonate; Separacion de Co{sup 2+} presente en solucion acuosa sobre carbonato de calcio

Energy Technology Data Exchange (ETDEWEB)

Garcia A, E.; Granados C, F. [ININ, Carretera Mexico-Toluca s/n, Ocoyoacac, Estado de Mexico (Mexico)

2008-07-01

The CaCO{sub 3} was synthesized by precipitation method and characterized using SEM, EDS, TGA and IR. It was studied the adsorption behavior of Co{sup 2+} present in aqueous solution on the synthesized material by experiments batch type at room temperature. Was found that removal of cobalt ions was greater than 40% indicating that this material can be used to remove Co{sup 2+} present in aqueous solution. (Author)

Effects of temperature and anion species on CO2 permeability and CO2/N2 separation coefficient through ionic liquid membranes

International Nuclear Information System (INIS)

Jindaratsamee, Pinyarat; Shimoyama, Yusuke; Morizaki, Hironobu; Ito, Akira

2011-01-01

The permeability of carbon dioxide (CO 2 ) through imidazolium-based ionic liquid membranes was measured by a sweep gas method. Six species of ionic liquids were studied in this work as follows: [emim][BF 4 ], [bmim][BF 4 ], [bmim][PF 6 ], [bmim][Tf 2 N], [bmim][OTf], and [bmim][dca]. The ionic liquids were supported with a polyvinylidene fluoride porous membrane. The measurements were performed at T = (303.15 to 343.15) K. The partial pressure difference between feed and permeate sides was 0.121 MPa. The permeability of the CO 2 increases with temperature for the all ionic liquid species. Base on solution diffusion theory, it can be explained that the diffusion coefficient of CO 2 in an ionic liquid affects the temperature dependence more strongly than the solubility coefficient. The greatest permeability was obtained with the [bmim][Tf 2 N] membrane. The membrane of [bmim][PF 6 ] presents the lowest permeability. The separation coefficient between CO 2 and N 2 through the ionic liquid membranes was also investigated at the volume fraction of CO 2 at feed side 0.10. The separation coefficient decreases with the increase of temperature for the all ionic liquid species. The membrane of [emim][BF 4 ] and [bmim][BF 4 ] gives the highest separation coefficient at constant temperature. The lowest separation coefficient was obtained from [bmim][Tf 2 N] membrane which presents the highest permeability of CO 2 .

High-Temperature Particulate Matter Filtration with Resilient Yttria-Stabilized ZrO2 Nanofiber Sponge.

Science.gov (United States)

Wang, Haolun; Lin, Sen; Yang, Shen; Yang, Xudong; Song, Jianan; Wang, Dong; Wang, Haiyang; Liu, Zhenglian; Li, Bo; Fang, Minghao; Wang, Ning; Wu, Hui

2018-05-01

Particulate matter (PM) is a major air pollutant in many regions, jeopardizing ecosystems and public health. Filtration at pollutant source is one of the most important ways to protect the environment, however, considering the high-temperature exhaust gas emissions, effective removal of PM and related pollutants from their sources remains a major challenge. In this study, a resilient, heat-resisting, and high-efficiency PM filter based on yttria-stabilized ZrO 2 (YSZ) nanofiber sponge produced with a scalable solution blow spinning process is reported. The porous 3D sponge composed of YSZ nanofibers is lightweight (density of 20 mg cm -3 ) and resilient at both room temperature and high temperatures. At room-temperature conditions, the YSZ nanofiber sponge exhibits 99.4% filtration efficiency for aerosol particles with size in the range of 20-600 nm, associated with a low pressure drop of only 57 Pa under an airflow velocity of 4.8 cm s -1 . At a high temperature of 750 °C, the ceramic sponge maintains a high filtration efficiency of 99.97% for PM 0.3-2.5 under a high airflow velocity of 10 cm s -1 . A practical vehicle exhaust filter to capture particles with filtration efficiency of >98.3% is also assembled. Hence, the YSZ nanofiber sponge has enormous potential to be applied in industry. © 2018 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

High-cycle fatigue behavior of Co-based superalloy 9CrCo at elevated temperatures

Directory of Open Access Journals (Sweden)

Wan Aoshuang

2016-10-01

Full Text Available A modified model is developed to characterize and evaluate high-cycle fatigue behavior of Co-based superalloy 9CrCo at elevated temperatures by considering the stress ratio effect. The model is informed by the relationship surface between maximum nominal stress, stress ratio and fatigue life. New formulae are derived to deal with the test data for estimating the parameters of the proposed model. Fatigue tests are performed on Co-based superalloy 9CrCo subjected to constant amplitude loading at four stress ratios of −1, −0.3, 0.5 and 0.9 in three environments of room temperature (i.e., about 25 °C and elevated temperatures of 530 °C and 620 °C, and the interaction mechanisms between the elevated temperature and stress ratio are deduced and compared with each other from fractographic studies. Finally, the model is applied to experimental data, demonstrating the practical and effective use of the proposed model. It is shown that new model has good correlation with experimental results.

DOES SOIL CO2 EFFLUX ACCLIMATIZETO ELEVATED TEMPERATURE AND CO2 DURING LONG-TERM TREATMENT OF DOUGLAS-FIR SEEDLINGS?

Science.gov (United States)

We investigated the effects of elevated soil temperature and atmospheric CO2 efflux (SCE) during the third an fourth years of study. We hypothesized that elevated temperature would stimulate SCE, and elevated CO2 would also stimulate SCE with the stimulation being greater at hig...

Effect of carbonation temperature on CO_2 adsorption capacity of CaO derived from micro/nanostructured aragonite CaCO_3

International Nuclear Information System (INIS)

Hlaing, Nwe Ni; Sreekantan, Srimala; Hinode, Hirofumi; Kurniawan, Winarto; Thant, Aye Aye; Othman, Radzali; Mohamed, Abdul Rahman; Salime, Chris

2016-01-01

Recent years, CaO-based synthetic materials have been attracted attention as potential adsorbents for CO_2 capture mainly due to their high CO_2 adsorption capacity. In this study, micro/nanostructured aragonite CaCO_3 was synthesized by a simple hydrothermal method with using polyacrylamide (PAM). The structural, morphological and thermal properties of the synthesized sample were investigated by X-ray diffraction (XRD), field-emission scanning electron microscopy (FESEM) and thermogravimetry analysis (TG-DTA). The XRD and FESEM results showed that the obtained sample was aragonite CaCO_3 with aggregated nanorods and microspheres composed of nanorods. A TG-DTA apparatus with Thermoplus 2 software was used to investigate the effect of carbonation temperature on the CO_2 adsorption capacity of CaO derived from aragonite CaCO_3 sample. At 300 °C, the sample reached the CO_2 adsorption capacity of 0.098 g-CO_2/g-adsorbent, whereas the sample achieved the highest capacity of 0.682 g-CO_2/g-adsorbent at 700 °C. The results showed that the carbonation temperature significantly influenced on the CO_2 adsorption capacity of the CaO derived from aragonite CaCO_3.

Inverse CeO2sbnd Fe2O3 catalyst for superior low-temperature CO conversion efficiency

Science.gov (United States)

Luo, Yongming; Chen, Ran; Peng, Wen; Tang, Guangbei; Gao, Xiaoya

2017-09-01

The paper presents a rational design of highly efficient and affordable catalysts for CO oxidation with a low operating temperature. A series of ceria-iron catalysts were inversely built via a co-precipitation method. The catalytic activity of low-temperature CO oxidation was much higher with CeO2-modified Fe2O3 (CeO2sbnd Fe2O3) than with Fe2O3-modified CeO2 (Fe2O3sbnd CeO2). In particular, the 7.5% CeO2sbnd Fe2O3 catalyst had the highest activity, reaching 96.17% CO conversion at just 25 °C. Catalyst characterization was carried out to explore the cause of the significantly different CO conversion efficiencies between the Fe2O3sbnd CeO2 and Fe2O3sbnd CeO2 catalysts. HRTEM showed a significant inhomogeneous phase in 7.5% CeO2sbnd Fe2O3 with small CeO2 nanoparticles highly dispersed on the rod-shaped Fe2O3 surface. Furthermore, the 7.5% CeO2sbnd Fe2O3 composite catalyst exhibited the highest ratios of Fe2+/Fe3+ and Ce3+/Ce4+ as well as the largest pore volume. These properties are believed to benefit the CO conversion in 7.5% CeO2sbnd Fe2O3.

Skeletal mineralogy of coral recruits under high temperature and pCO2

Directory of Open Access Journals (Sweden)

T. Foster

2016-03-01

Our results show that elevated pCO2 alone is unlikely to drive changes in the skeletal mineralogy of young corals. Not having an ability to switch from aragonite to calcite precipitation may leave corals and ultimately coral reef ecosystems more susceptible to predicted ocean acidification. An important area for prospective research would be the investigation of the combined impact of high pCO2 and reduced Mg ∕ Ca ratio on coral skeletal mineralogy.

Development of a Next-Generation Membrane-Integrated Adsorption Processor for CO2 Removal and Compression for Closed-Loop Air Revitalization Systems

Science.gov (United States)

Mulloth, Lila; LeVan, Douglas

2002-01-01

The current CO2 removal technology of NASA is very energy intensive and contains many non-optimized subsystems. This paper discusses the concept of a next-generation, membrane integrated, adsorption processor for CO2 removal nd compression in closed-loop air revitalization systems. This processor will use many times less power than NASA's current CO2 removal technology and will be capable of maintaining a lower CO2 concentration in the cabin than that can be achieved by the existing CO2 removal systems. The compact, consolidated, configuration of gas dryer, CO2 separator, and CO2 compressor will allow continuous recycling of humid air in the cabin and supply of compressed CO2 to the reduction unit for oxygen recovery. The device has potential application to the International Space Station and future, long duration, transit, and planetary missions.

Elevated temperature and CO2 concentration effects on xylem anatomy of Scots pine

International Nuclear Information System (INIS)

Kilpelainen, A.; Gerendiain, A.Z.; Luostarinen, K.; Peltola, H.; Kellomaki, S.

2007-01-01

The effects of carbon dioxide (CO 2 ) concentrations and elevated temperatures on the xylem anatomy of 20-year old Scots pine trees were investigated. The experiment was conducted in 16 chambers containing 4 trees each with a factorial combination of both ambient and elevated CO 2 concentrations and 2 different temperature regimes. CO 2 concentrations were doubled with a corresponding increase of between 2 and 6 degrees C according to each season over a period of 6 years. The study showed that elevated CO 2 concentrations increased the ring width in 4 of the 6 analyzed treatment years. Earlywood width increased during the first 2 years of the experiment, while latewood width increased during the third year of the study. The study also showed that the tracheid walls in both the latewood and earlywood samples were thicker when either temperature levels or CO 2 levels were increased. It was noted that combined CO 2 and temperature elevations resulted in thinner tracheid walls. However, latewood tracheid lumen diameters were larger in all CO 2 and temperature treatments than trees grown in ambient conditions. It was concluded that xylem anatomy was impacted more by increases in temperature than by elevated CO 2 concentrations. 48 refs., 2 tabs., 6 figs

High temperature fluidized bed zero valent iron process for flue gas nitrogen monoxide removal

International Nuclear Information System (INIS)

Cheng, C.Y.; Chen, S.S.; Tang, C.H.; Chang, Y.M.; Cheng, H.H.; Liu, H.L.

2008-01-01

Nitrogen oxides (NO x ) are generated from a variety of sources, and are critical components of photochemical smog. Zero valent iron (ZVI) has been used to remove NO x in a number of studies. The ZVI process requires no extra chemicals or catalysts. In this study, a fluidized ZVI process for removing NO x from flue gases was proposed. The study examined the effects of temperature, ZVI dosage and influent NO concentrations, and observed the kinetic effects between the fluidized ZVI and NO x . A life cycle analysis of the process was also provided. The parametric analysis was conducted in a series of column studies using a continuous emissions monitoring system. Minimum fluidization velocity equations were provided, and the drag coefficient was determined. Capacities of ZVI for NO removal at different temperatures were calculated. Results of the study suggested that temperature, influent concentrations, and flow rates all influenced kinetic coefficients. Different temperatures resulted in different rates of NO removal. It was concluded that between 673 K and 773 K, almost complete NO removals were achieved. 14 refs., 2 tabs., 9 figs

Linde Rectiscol{reg_sign} process. The most economic and experienced wash process for removal of sulfur compounds and CO{sub 2} from gasification gases

Energy Technology Data Exchange (ETDEWEB)

Kaballo, H.-P.; Kerestceciogly, U. [Linde AG, Hoellriegelskreuth (Germany). Linde Engineering Division

2006-07-01

The Recitsol{reg_sign} wash process is a well-proven process for the removal of H{sub 2}S/COS and CO{sub 2} from coal, asphalt, pitch or oil derived synthesis gas. It is a physical gas wash system using methanol as solvent at operating temperatures below water freezing point, to produce a synthesis gas with less than 0.1 vppm of total sulfur. The CO{sub 2} content can be adjusted in a range from several mol-percent down to a few ppm, as is required by the specified application. Its main advantages are the use of cheap and readily available methanol as solvent, the very flexible process configuration, and rather low utility consumption figures compared with other wash processes, like PEGE based process or chemical washes. A modern concept of a Rectisol{reg_sign} unit is described, to treat shifted and un-shifted gases in just one plant: shifted gas was used for hydrotreating in a refinery. Unshifted gas was used as fuel gas for power generation in an IGCC. CO{sub 2} of the unshifted feed gas was removed only partly, because the remaining CO{sub 2} was fed as inert gas together with the fuel gas to an IGCC. All sulfur compounds of both feed gases were concentrated in one single stream with a high H{sub 2}S concentration. Impurities like NH{sub 3}, HCN or metal carbonyls were eliminated nearly quantitatively. 4 refs., 4 figs., 3 tabs.

Functionalized layered double hydroxide with nitrogen and sulfur co-decorated carbondots for highly selective and efficient removal of soft Hg2+ and Ag+ ions.

Science.gov (United States)

Asiabi, Hamid; Yamini, Yadollah; Shamsayei, Maryam; Molaei, Karam; Shamsipur, Mojtaba

2018-05-28

A facile composite was fabricated via direct assembly of nitrogen and sulfur co-decorated carbon dots with abundant oxygen-containing functional groups on the surface of the positively charged layered double hydroxide (N,S-CDs-LDH). The novel N,S-CDs-LDH demonstrates highly selective bindings (M-S) and an extremely efficient removal capacity for soft metal ions such as Ag + and Hg 2+ ions. N,S-CDs-LDH displayed a selectivity order of Ag + > Hg 2+ > Cu 2+ > Pb 2+ > Zn 2+ > Cd 2+ for their adsorption. The enormous capacities for Hg 2+ (625.0 mg g -1 ) and Ag + (714.3 mg g -1 ) and very high distribution coefficients (K d ) of 9.9 × 10 6 mL g -1 (C 0  = 20 mg L -1 ) and 2.0 × 10 7 mL g -1 (C 0  = 20 mg L -1 ) for Hg 2+ and Ag + , respectively, place the N,S-CDs-LDH at the top of LDH based materials known for such removal. The adsorption kinetic curves for Hg 2+ and Ag + fitted well with the pseudo-second order model. For Hg 2+ and Ag + , an exceptionally rapid capture with removal ∼100% within 80 min was observed (C ions  = 30 mg L -1 and V/m ratio of 1000). The adsorption isotherms were well described using Langmuir isotherm. The N,S-CDs-LDH was successfully applied to highly efficient removal of Hg 2+ and Ag + from aqueous solutions. Copyright © 2018 Elsevier B.V. All rights reserved.

Room temperature CO and H2 sensing with carbon nanoparticles

International Nuclear Information System (INIS)

Kim, Daegyu; Pikhitsa, Peter V; Yang, Hongjoo; Choi, Mansoo

2011-01-01

We report on a shell-shaped carbon nanoparticle (SCNP)-based gas sensor that reversibly detects reducing gas molecules such as CO and H 2 at room temperature both in air and inert atmosphere. Crystalline SCNPs were synthesized by laser-assisted reactions in pure acetylene gas flow, chemically treated to obtain well-dispersed SCNPs and then patterned on a substrate by the ion-induced focusing method. Our chemically functionalized SCNP-based gas sensor works for low concentrations of CO and H 2 at room temperature even without Pd or Pt catalysts commonly used for splitting H 2 molecules into reactive H atoms, while metal oxide gas sensors and bare carbon-nanotube-based gas sensors for sensing CO and H 2 molecules can operate only at elevated temperatures. A pristine SCNP-based gas sensor was also examined to prove the role of functional groups formed on the surface of functionalized SCNPs. A pristine SCNP gas sensor showed no response to reducing gases at room temperature but a significant response at elevated temperature, indicating a different sensing mechanism from a chemically functionalized SCNP sensor.

Biological phosphorus removal during high-rate, low-temperature, anaerobic digestion of wastewater

Directory of Open Access Journals (Sweden)

Ciara eKeating

2016-03-01

Full Text Available We report, for the first time, extensive biologically-mediated phosphate removal from wastewater during high-rate anaerobic digestion (AD. A hybrid sludge bed/fixed-film (packed pumice stone reactor was employed for low-temperature (12°C anaerobic treatment of synthetic sewage wastewater. Successful phosphate removal from the wastewater (up to 78% of influent phosphate was observed, mediated by biofilms in the reactor. Scanning electron microscopy and energy dispersive X-ray analysis revealed the accumulation of elemental phosphorus (~2% within the sludge bed and fixed-film biofilms. 4’, 6-diamidino-2-phenylindole (DAPI staining indicated phosphorus accumulation was biological in nature and mediated through the formation of intracellular inorganic polyphosphate (polyP granules within these biofilms. DAPI staining further indicated that polyP accumulation was rarely associated with free cells. Efficient and consistent chemical oxygen demand (COD removal was recorded, throughout the 732-day trial, at applied organic loading rates between 0.4-1.5 kg COD m-3 d-1 and hydraulic retention times of 8-24 hours, while phosphate removal efficiency ranged from 28-78% on average per phase. Analysis of protein hydrolysis kinetics and the methanogenic activity profiles of the biomass revealed the development, at 12˚C, of active hydrolytic and methanogenic populations. Temporal microbial changes were monitored using Illumina Miseq analysis of bacterial and archaeal 16S rRNA gene sequences. The dominant bacterial phyla present in the biomass at the conclusion of the trial were the Proteobacteria and Firmicutes and the dominant archaeal genus was Methanosaeta. Trichococcus and Flavobacterium populations, previously associated with low temperature protein degradation, developed in the reactor biomass. The presence of previously characterised polyphosphate accumulating organisms (PAOs such as Rhodocyclus, Chromatiales, Actinobacter and Acinetobacter was

HCl removal using cycled carbide slag from calcium looping cycles

International Nuclear Information System (INIS)

Xie, Xin; Li, Yingjie; Wang, Wenjing; Shi, Lei

2014-01-01

Highlights: • Cycled carbide slag from calcium looping cycles is used to remove HCl. • The optimum temperature for HCl removal of cycled carbide slag is 700 °C. • The presence of CO 2 restrains HCl removal of cycled carbide slag. • CO 2 capture conditions have important effects on HCl removal of cycled carbide slag. • HCl removal capacity of carbide slag drops with cycle number rising from 1 to 50. - Abstract: The carbide slag is an industrial waste from chlor-alkali plants, which can be used to capture CO 2 in the calcium looping cycles, i.e. carbonation/calcination cycles. In this work, the cycled carbide slag from the calcium looping cycles for CO 2 capture was proposed to remove HCl in the flue gas from the biomass-fired and RDFs-fired boilers. The effects of chlorination temperature, HCl concentration, particle size, presence of CO 2 , presence of O 2 , cycle number and CO 2 capture conditions in calcium looping cycles on the HCl removal behavior of the carbide slag experienced carbonation/calcination cycles were investigated in a triple fixed-bed reactor. The chlorination product of the cycled carbide slag from the calcium looping after absorbing HCl is not CaCl 2 but CaClOH. The optimum temperature for HCl removal of the cycled carbide slag from the carbonation/calcination cycles is 700 °C. The chlorination conversion of the cycled carbide slag increases with increasing the HCl concentration. The cycled carbide slag with larger particle size exhibits a lower chlorination conversion. The presence of CO 2 decreases the chlorination conversions of the cycled carbide slag and the presence of O 2 has a trifling impact. The chlorination conversion of the carbide slag experienced 1 carbonation/calcination cycle is higher than that of the uncycled calcined sorbent. As the number of carbonation/calcination cycles increases from 1 to 50, the chlorination conversion of carbide slag drops gradually. The high calcination temperature and high CO 2

Separation of Co2+ present in aqueous solution on calcium carbonate

International Nuclear Information System (INIS)

Garcia A, E.; Granados C, F.

2008-01-01

The CaCO 3 was synthesized by precipitation method and characterized using SEM, EDS, TGA and IR. It was studied the adsorption behavior of Co 2+ present in aqueous solution on the synthesized material by experiments batch type at room temperature. Was found that removal of cobalt ions was greater than 40% indicating that this material can be used to remove Co 2+ present in aqueous solution. (Author)

High-cycle fatigue behavior of Co-based superalloy 9CrCo at elevated temperatures

OpenAIRE

Wan, Aoshuang; Xiong, Junjiang; Lyu, Zhiyang; Li, Kuang; Du, Yisen; Chen, Kejiao; Man, Ziyu

2016-01-01

A modified model is developed to characterize and evaluate high-cycle fatigue behavior of Co-based superalloy 9CrCo at elevated temperatures by considering the stress ratio effect. The model is informed by the relationship surface between maximum nominal stress, stress ratio and fatigue life. New formulae are derived to deal with the test data for estimating the parameters of the proposed model. Fatigue tests are performed on Co-based superalloy 9CrCo subjected to constant amplitude loading a...

Thiophene hydrodesulfurization over CoMo/Al2O3-CuY catalysts: Temperature effect study

Directory of Open Access Journals (Sweden)

Yamina Boukoberine

2016-09-01

Full Text Available CoMo/γ-Al2O3-CuY catalysts are prepared by physically mixing CoMo/γ-Al2O3 catalyst with Cu-exchanged Y zeolite. The CuY zeolite is prepared by the solid state ion exchange technique. The thiophene hydrodesulfurization is performed in a fixed bed reactor at high temperature and atmospheric pressure. The results show that the presence of CuY zeolite particles in CoMo/Al2O3 catalyst can have a noticeable effect on both the conversion and product selectivities. An increasing zeolite loading in catalyst results in a decrease of the thiophene HDS activity. This decrease is probably caused by the formation of heavy compounds and the deactivation of the zeolite at high temperatures.

Improvement of soluble coffee aroma using an integrated process of supercritical CO2 extraction with selective removal of the pungent volatiles by adsorption on activates carbon

Directory of Open Access Journals (Sweden)

S. Lucas

2006-06-01

Full Text Available In this paper a two-step integrated process consisting of CO2 supercritical extraction of volatile coffee compounds (the most valuable from roasted and milled coffee, and a subsequent step of selective removal of pungent volatiles by adsorption on activated carbon is presented. Some experiments were carried out with key compounds from roasted coffee aroma in order to study the adsorption step: ethyl acetate as a desirable compound and furfural as a pungent component. Operational parameters such as adsorption pressure and temperature and CO2 flowrate were optimized. Experiments were conducted at adsorption pressures of 12-17 MPa, adsorption temperatures of 35-50ºC and a solvent flow rate of 3-5 kg/h. In all cases, the solute concentration and the activated particle size were kept constant. Results show that low pressures (12 MPa, low temperatures (35ºC and low CO2 flowrates (3 kg/h are suitable for removing the undesirable pungent and smell components (e.g. furfural and retaining the desirable aroma compounds (e.g. ethyl acetate. The later operation with real roasted coffee has corroborated the previous results obtained with the key compounds.

Mechanism of the CO2-Ca(OH)2 reaction

International Nuclear Information System (INIS)

Chew, V.S.; Cheh, C.H.; Glass, R.W.

1983-01-01

Recent studies clearly showed the importance of moisture in achieving high Ca(OH) 2 absorbent utilization for removing CO 2 from gas streams at ambient temperatures. However, the role of moisture and the mechanism of the reaction was not well understood. This paper summarizes the results of a study of the mechanism of the CO 2 -Ca(OH) 2 reaction with emphasis on the role of moisture. The reaction between Ca(OH) 2 and CO 2 in moist N 2 was found to be first order with respect to the reactants with a rate constant of about 100 min -1 . At high humidities, the rate of reaction was chemically controlled, but at low humidities, the reaction rate was limited by the diffusion through the carbonate layer formed by the reaction. Calculations showed that capillary condensation could have occurred only in about 2% of the pore volume and was unlikely to have affected the reaction rate significantly by allowing the reaction to occur in the liquid phase. It was, therefore, concluded that the main role of moisture was to improve the Ca(OH) 2 utilization by lowering the resistance to diffusion through the carbonate layer

CFD simulation of CO_2 sorption on K_2CO_3 solid sorbent in novel high flux circulating-turbulent fluidized bed riser: Parametric statistical experimental design study

International Nuclear Information System (INIS)

Thummakul, Theeranan; Gidaspow, Dimitri; Piumsomboon, Pornpote; Chalermsinsuwan, Benjapon

2017-01-01

Highlights: • Circulating-turbulent fluidization was proved to be advantage on CO_2 sorption. • The novel regime was proven to capture CO_2 higher than the conventional regimes. • Uniform solid particle distribution was observed in the novel fluidization regime. • The system continuity had more effect in the system than the process system mixing. • Parametric experimental design analysis was studied to evaluate significant factor. - Abstract: In this study a high flux circulating-turbulent fluidized bed (CTFB) riser was confirmed to be advantageous for carbon dioxide (CO_2) sorption on a potassium carbonate solid sorbent. The effect of various parameters on the CO_2 removal level was evaluated using a statistical experimental design. The most appropriate fluidization regime was found to occur between the turbulent and fast fluidization regimes, which was shown to capture CO_2 more efficiently than conventional fluidization regimes. The highest CO_2 sorption level was 93.4% under optimized CTFB operating conditions. The important parameters for CO_2 capture were the inlet gas velocity and the interactions between the CO_2 concentration and the inlet gas velocity and water vapor concentration. The CTFB regime had a high and uniform solid particle distribution in both the axial and radial system directions and could transport the solid sorbent to the regeneration reactor. In addition, the process system continuity had a stronger effect on the CO_2 removal level in the system than the process system mixing.

Emission of OH* and CO2* during the high-temperature oxidation of acetone in reflected shock waves

Science.gov (United States)

Tereza, A. M.; Smirnov, V. N.; Vlasov, P. A.; Shumova, V. V.; Garmash, A. A.

2018-01-01

Experimental and kinetic modeling study of the ignition of a stoichiometric mixture of acetone with oxygen diluted by argon was carried out behind reflected shock waves within the temperature range of 1350-1810 K for the total mixture concentration [M 50] ~ 10-5 mol/cm3. Emission signals were recorded simultaneously for three different wavelengths: OH* (λ = 308 nm) and {{{CO}}}2* (λ1 = 365 nm; λ2 = 451 nm). It was revealed that the time it takes to reach the maximum of emission of OH* and {{{CO}}}2* is practically the same over the whole temperature range. At the same time, the emission profiles of {{{CO}}}2* after the maximum was attained, recorded at λ2 = 451 nm, differ noticeably from the profiles recorded at λ1 = 365 nm. For numerical modeling of the emission profiles of OH* and {{{CO}}}2* , the corresponding sets of excitation and quenching reactions available in the literature were used. In the course of our numerical simulations we succeeded in good agreement of our own experimental and simulation results on acetone ignition and the results available in the literature for conditions under consideration.

Multimodel Surface Temperature Responses to Removal of U.S. Sulfur Dioxide Emissions

Science.gov (United States)

Conley, A. J.; Westervelt, D. M.; Lamarque, J.-F.; Fiore, A. M.; Shindell, D.; Correa, G.; Faluvegi, G.; Horowitz, L. W.

2018-03-01

Three Earth System models are used to derive surface temperature responses to removal of U.S. anthropogenic SO2 emissions. Using multicentury perturbation runs with and without U.S. anthropogenic SO2 emissions, the local and remote surface temperature changes are estimated. In spite of a temperature drift in the control and large internal variability, 200 year simulations yield statistically significant regional surface temperature responses to the removal of U.S. SO2 emissions. Both local and remote surface temperature changes occur in all models, and the patterns of changes are similar between models for northern hemisphere land regions. We find a global average temperature sensitivity to U.S. SO2 emissions of 0.0055 K per Tg(SO2) per year with a range of (0.0036, 0.0078). We examine global and regional responses in SO4 burdens, aerosol optical depths (AODs), and effective radiative forcing (ERF). While changes in AOD and ERF are concentrated near the source region (United States), the temperature response is spread over the northern hemisphere with amplification of the temperature increase toward the Arctic. In all models, we find a significant response of dust concentrations, which affects the AOD but has no obvious effect on surface temperature. Temperature sensitivity to the ERF of U.S. SO2 emissions is found to differ from the models' sensitivity to radiative forcing of doubled CO2.

Above room temperature ferromagnetism in Si:Mn and TiO(2-delta)Co.

Science.gov (United States)

Granovsky, A; Orlov, A; Perov, N; Gan'shina, E; Semisalova, A; Balagurov, L; Kulemanov, I; Sapelkin, A; Rogalev, A; Smekhova, A

2012-09-01

We present recent experimental results on the structural, electrical, magnetic, and magneto-optical properties of Mn-implanted Si and Co-doped TiO(2-delta) magnetic oxides. Si wafers, both n- and p-type, with high and low resistivity, were used as the starting materials for implantation with Mn ions at the fluencies up to 5 x 10(16) cm(-2). The saturation magnetization was found to show the lack of any regular dependence on the Si conductivity type, type of impurity and the short post-implantation annealing. According to XMCD Mn impurity in Si does not bear any appreciable magnetic moment at room temperature. The obtained results indicate that above room temperature ferromagnetism in Mn-implanted Si originates not from Mn impurity but rather from structural defects in Si. The TiO(2-delta):Co thin films were deposited on LaAlO3 (001) substrates by magnetron sputtering in the argon-oxygen atmosphere at oxygen partial pressure of 2 x 10(-6)-2 x 10(-4) Torr. The obtained transverse Kerr effect spectra at the visible and XMCD spectra indicate on intrinsic room temperature ferromagnetism in TiO(2-delta):Co thin films at low (< 1%) volume fraction of Co.

Projected near-future levels of temperature and pCO2 reduce coral fertilization success.

Directory of Open Access Journals (Sweden)

Rebecca Albright

Full Text Available Increases in atmospheric carbon dioxide (pCO2 are projected to contribute to a 1.1-6.4°C rise in global average surface temperatures and a 0.14-0.35 reduction in the average pH of the global surface ocean by 2100. If realized, these changes are expected to have negative consequences for reef-building corals including increased frequency and severity of coral bleaching and reduced rates of calcification and reef accretion. Much less is known regarding the independent and combined effects of temperature and pCO2 on critical early life history processes such as fertilization. Here we show that increases in temperature (+3°C and pCO2 (+400 µatm projected for this century negatively impact fertilization success of a common Indo-Pacific coral species, Acropora tenuis. While maximum fertilization did not differ among treatments, the sperm concentration required to obtain 50% of maximum fertilization increased 6- to 8- fold with the addition of a single factor (temperature or CO2 and nearly 50- fold when both factors interact. Our results indicate that near-future changes in temperature and pCO2 narrow the range of sperm concentrations that are capable of yielding high fertilization success in A. tenuis. Increased sperm limitation, in conjunction with adult population decline, may have severe consequences for coral reproductive success. Impaired sexual reproduction will further challenge corals by inhibiting population recovery and adaptation potential.

High hardness-high toughness WC-20Co nanocomposites: Effect of VC variation and sintering temperature

International Nuclear Information System (INIS)

Kumar, Devender; Singh, K.

2016-01-01

WC-Co nanocomposites with variable VC content are synthesized by liquid phase sintering at two different temperatures. The as synthesized samples are characterized by X-ray diffraction (XRD), field emission scanning electron microscope (FE-SEM) and optical microscope. The mechanical properties are obtained by Vickers indentation method. The high content of VC, lead to high porosity when sintering temperature is increased from 1350 to 1400 °C. The relative density of all the samples is more than 95%. Microstructure reveals that agglomeration of W-Co-C and V-W-C increases at 1400 °C, which generates layered interfaces in radial direction and hence the material inhomogeneity. XRD pattern shows that the formation of η phase increases at 1400 °C, which is responsible to decrease the fracture toughness of the present samples. The average particle size of 102 nm, highest hardness of 1870.6 kgf/mm"2 with fracture toughness of 14.4 MN/mm"3"/"2 is observed in sample having 7.5 wt% VC, sintered at 1350 °C for one minute. This combination shows the highest hardness and reasonably high toughness as compared to conventionally sintered materials reported so far.

Influx of CO2 from Soil Incubated Organic Residues at Constant Temperature

Directory of Open Access Journals (Sweden)

Shoukat Ali Abro

2016-06-01

Full Text Available Temperature induced CO2 from genotypic residue substances is still less understood. Two types of organic residues (wheat- maize were incubated at a constant temperature (25°C to determine the rate and cumulative influx of CO2 in laboratory experiment for 40 days. Further, the effect of surface and incorporated crop residues with and without phosphorus addition was also studied. Results revealed that mixing of crop residues increased CO2-C evolution significantly & emission rare was 37% higher than that of control. At constant temperature, soil mixed residues, had higher emission rates CO2-C than the residues superimposed. There was linear correlation of CO2-C influxed for phosphorus levels and residue application ways with entire incubation at constant temperature. The mixing of organic residues to soil enhanced SOC levels and biomass of microbially bound N; however to little degree ammonium (NH4-N and nitrate NO3-N nitrogen were decreased.

Effects of CO2 and temperature on tritrophic interactions.

Directory of Open Access Journals (Sweden)

Lee A Dyer

Full Text Available There has been a significant increase in studies of how global change parameters affect interacting species or entire communities, yet the combined or interactive effects of increased atmospheric CO2 and associated increases in global mean temperatures on chemically mediated trophic interactions are mostly unknown. Thus, predictions of climate-induced changes on plant-insect interactions are still based primarily on studies of individual species, individual global change parameters, pairwise interactions, or parameters that summarize communities. A clear understanding of community response to global change will only emerge from studies that examine effects of multiple variables on biotic interactions. We examined the effects of increased CO2 and temperature on simple laboratory communities of interacting alfalfa, chemical defense, armyworm caterpillars, and parasitoid wasps. Higher temperatures and CO2 caused decreased plant quality, decreased caterpillar development times, developmental asynchrony between caterpillars and wasps, and complete wasp mortality. The effects measured here, along with other effects of global change on natural enemies suggest that biological control and other top-down effects of insect predators will decline over the coming decades.

Linearity between temperature peak and bio-energy CO2 emission rates

International Nuclear Information System (INIS)

Cherubini, Francesco; Bright, Ryan M.; Stromman, Anders H.; Gasser, Thomas; Ciais, Philippe

2014-01-01

Many future energy and emission scenarios envisage an increase of bio-energy in the global primary energy mix. In most climate impact assessment models and policies, bio-energy systems are assumed to be carbon neutral, thus ignoring the time lag between CO 2 emissions from biomass combustion and CO 2 uptake by vegetation. Here, we show that the temperature peak caused by CO 2 emissions from bio-energy is proportional to the maximum rate at which emissions occur and is almost insensitive to cumulative emissions. Whereas the carbon-climate response (CCR) to fossil fuel emissions is approximately constant, the CCR to bio-energy emissions depends on time, biomass turnover times, and emission scenarios. The linearity between temperature peak and bio-energy CO 2 emission rates resembles the characteristic of the temperature response to short-lived climate forcers. As for the latter, the timing of CO 2 emissions from bio-energy matters. Under the international agreement to limit global warming to 2 C by 2100, early emissions from bio-energy thus have smaller contributions on the targeted temperature than emissions postponed later into the future, especially when bio-energy is sourced from biomass with medium (50-60 years) or long turnover times (100 years). (authors)

High-temperature thermoelectric properties of AgxYyCa2⋅ 8Co4O9 ...

Indian Academy of Sciences (India)

temperature thermoelectric properties of AgYCa2.8Co4O9 + ceramics. Youjin Zheng Hui Zhou Tengzhou Ma Guihong Zuo Hongtao Li Taichao Su Chunlei Wu Hailiang Huang Dan Wang Longcheng Yin. Volume 37 Issue 5 August 2014 pp 963- ...

Absorption capacity and viscosity for CO_2 capture process using high concentrated PZ-DEAE aqueous solution

International Nuclear Information System (INIS)

Fu, Dong; Wang, LeMeng; Mi, ChenLu; Zhang, Pan

2016-01-01

Highlights: • Absorption of CO_2 in high concentrated DEAE-PZ aqueous solutions were measured. • Viscosities of CO_2-unloaded and CO_2-loaded DEAE-PZ aqueous solutions were measured. • Weiland equation was used to calculate the viscosities. • Effects of temperature, concentration and CO_2 loading on viscosity were demonstrated. - Abstract: The absorption capacity of CO_2 in piperazine (PZ) promoted 2-diethylaminoethanol (DEAE) aqueous solution was measured. The viscosities of both CO_2-unloaded and CO_2-loaded PZ-DEAE aqueous solutions were measured and then modelled. The temperatures ranged from 303.2 K to 323.2 K. The mass fraction of PZ and DEAE respectively ranged from 0 to 0.075 and 0.3 to 0.5. The temperature and concentration dependences of absorption capacity were determined. The effects of temperature, mass fraction and CO_2 loading on viscosities are demonstrated.

Highly anisotropic SmCo5 nanoflakes by surfactant-assisted ball milling at low temperature

International Nuclear Information System (INIS)

Liu, Lidong; Zhang, Songlin; Zhang, Jian; Ping Liu, J.; Xia, Weixing; Du, Juan; Yan, Aru; Yi, Jianhong; Li, Wei; Guo, Zhaohui

2015-01-01

Surfactant-assisted ball milling (SABM) has been shown to be a promising method for preparing rare earth-transition metal (RE-TM) nanoflakes and nanoparticles. In this work, we prepared SmCo 5 nanoflakes by SABM at low temperature, and 2-methyl pentane and trioctylamine were specially selected as solvent and surfactant, respectively, due to their low melting points. The effects of milling temperature on the morphology, microstructure and magnetic performance of SmCo 5 nanoflakes were investigated systematically. Comparing with the samples milled at room temperature, the SmCo 5 nanoflakes prepared at low temperature displayed more homogeneous morphology and lower oxygen content. Remarkably, better crystallinity, better grain alignment and larger remanence ratio were shown in the samples milled at low temperature, which resulted from the distinct microstructure caused by low milling temperature. The differences in structural evolution between the SmCo 5 nanoflakes milled at room temperature and low temperature, including the formation of nanocrystalline, grain boundary sliding, grain rotation, et al., were discussed. It was found that lowering the temperature of SABM was a powerful method for the fabrication of RE-TM nanoflakes, which showed better hard magnetic properties and lower oxygen content. This was important for the preparation of high-performance sintered magnets, bonded magnets and nanocomposite magnets. - Highlights: • We prepare SmCo 5 nanoflakes by surfactant-assisted ball milling at low temperature. • Better grain alignment and higher remanence ratio are achieved. • The oxygen content is reduced by lowering the milling temperature. • A distinct microstructural evolution caused by low milling temperature is clarified

Regenerative process for removal of mercury and other heavy metals from gases containing H.sub.2 and/or CO

Science.gov (United States)

Jadhav, Raja A [Naperville, IL

2009-07-07

A method for removal of mercury from a gaseous stream containing the mercury, hydrogen and/or CO, and hydrogen sulfide and/or carbonyl sulfide in which a dispersed Cu-containing sorbent is contacted with the gaseous stream at a temperature in the range of about 25.degree. C. to about 300.degree. C. until the sorbent is spent. The spent sorbent is contacted with a desorbing gaseous stream at a temperature equal to or higher than the temperature at which the mercury adsorption is carried out, producing a regenerated sorbent and an exhaust gas comprising released mercury. The released mercury in the exhaust gas is captured using a high-capacity sorbent, such as sulfur-impregnated activated carbon, at a temperature less than about 100.degree. C. The regenerated sorbent may then be used to capture additional mercury from the mercury-containing gaseous stream.

Flow behavior and microstructures of powder metallurgical CrFeCoNiMo0.2 high entropy alloy during high temperature deformation

Energy Technology Data Exchange (ETDEWEB)

Wang, Jiawen [State Key Laboratory of Powder Metallurgy, Central South University, Changsha 410083 (China); Liu, Yong, E-mail: yonliu@csu.edu.cn [State Key Laboratory of Powder Metallurgy, Central South University, Changsha 410083 (China); Liu, Bin, E-mail: binliu@csu.edu.cn [State Key Laboratory of Powder Metallurgy, Central South University, Changsha 410083 (China); Wang, Yan [School of Aeronautics and Astronautics, Central South University, Changsha 410083 (China); Cao, Yuankui; Li, Tianchen; Zhou, Rui [State Key Laboratory of Powder Metallurgy, Central South University, Changsha 410083 (China)

2017-03-24

Dynamic recrystallization (DRX) refine grains of high entropy alloys (HEAs) and significant improve the mechanical property of HEAs, but the effect of high melting point element molybdenum (Mo) on high temperature deformation behavior has not been fully understood. In the present study, flow behavior and microstructures of powder metallurgical CrFeCoNiMo{sub 0.2} HEA were investigated by hot compression tests performed at temperatures ranging from 700 to 1100 °C with strain rates from 10{sup −3} to 1 s{sup −1}. The Arrhenius constitutive equation with strain-dependent material constants was used for modeling and prediction of flow stress. It was found that at 700 °C, the dynamic recovery is the dominant softening mechanism, whilst with the increase in compression testing temperature, the DRX becomes the dominant mechanism of softening. In the present HEA, the addition of Mo results in the high activation energy (463 kJ mol{sup −1}) and the phase separation during hot deformation. The formation of Mo-rich σ phase particles pins grain boundary migration during DRX, and therefore refines the size of recrystallized grains.

Thermal analysis and temperature dependent dielectric responses of Co doped anatase TiO2 nanoparticles

International Nuclear Information System (INIS)

Alamgir; Khan, Wasi; Ahammed, Nashiruddin; Naqvi, A. H.; Ahmad, Shabbir

2015-01-01

Nanoparticles (NPs) of pure and 5 mol % cobalt doped TiO 2 synthesized through acid modified sol-gel method were characterized to understand their thermal, structural, morphological, and temperature dependent dielectric properties. Thermogravimetric analysis (TGA) has been used for thermal studies and indicates the weight loss in two steps due to the removal of residual organics. X-ray diffraction study was employed to confirm the formation of single anatase phase with tetragonal symmetry for both pure and 5 mol % Co doped TiO 2 NPs. The average crystallite size of both samples was calculated from the Scherrer’s formula and was found in the range from 9-11 nm. TEM micrographs of these NPs reflect their shape and distribution. The dielectric constant (ε′), dielectric loss (tanδ) and ac conductivity (σ ac ) were also studied as a function of temperature at different frequencies. Electrical responses of the synthesized NPs have been analyzed carefully in the framework of relevant models. It is also noticed that the dielectric constant (ε′) of the samples found to decrease with increasing frequency but increases with increasing temperature up to a particular value and then sharply decreases. Temperature variation of dielectric constant exhibits step like escalation and shows relaxation behavior. Study of dielectric properties shows dominant dependence on the grain size as well as Co ion incorporation in TiO 2

Acidic sweep gas with carbonic anhydrase coated hollow fiber membranes synergistically accelerates CO2 removal from blood

OpenAIRE

Arazawa, D. T.; Kimmel, J. D.; Finn, M.C.; Federspiel, W. J.

2015-01-01

The use of extracorporeal carbon dioxide removal (ECCO2R) is well established as a therapy for patients suffering from acute respiratory failure. Development of next generation low blood flow (< 500 mL/min) ECCO2R devices necessitates more efficient gas exchange devices. Since over 90% of blood CO2 is transported as bicarbonate (HCO3−), we previously reported development of a carbonic anhydrase (CA) immobilized bioactive hollow fiber membrane (HFM) which significantly accelerates CO2 removal ...

Effects of increased temperature and CO{sub 2} on soil quality

Energy Technology Data Exchange (ETDEWEB)

Ogner, G.

1996-03-01

This paper was read at the workshop ``The Norwegian Climate and Ozone Research Programme`` held on 11-12 March 1996. The Norwegian Forest Research Institute has studied the effects of increased CO{sub 2} and temperature on forest soil, soil leachate and plants in an open top chamber experiment. The purpose was to analyze the changes in soil parameters and the leaching of elements. Nitrate and aluminium received special attention. The growth of Norway spruce and birch was followed, and its impact on the soil parameters. Preliminary results indicate that the temperature increase of the soil and consequently an increased turnover of soil organic matter had the major effect on the quality of soil leachates. CO{sub 2} was less important. Leaching of NO{sub 3}{sup -} was high from control lysimeters with moss cover. Lysimeters with birch hardly leached NO{sub 3}{sup -} at all. Spruce is in an intermediate position. Increased leaching of Al{sup n+} is found for moss lysimeters. Leachates from birch lysimeters have high concentrations of Al{sup n+} only at the end of the growth seasons. Plant growth is to some extent increased by the CO{sub 2} treatment. Birch grew well in all lysimeters and all treatments, spruce developed clear symptoms of stress. This result does not fit with the increased availability of nutrients in soil solution

High-temperature Thermoelectric and Microstructural Characteristics of Ga Substituted on the Co-site in Cobalt-based Oxides

DEFF Research Database (Denmark)

Van Nong, Ngo; Yanagiya, S.; Sonne, Monica

2011-01-01

The effects of Ga substitution on the Co-site on the high-temperature thermoelectric properties and microstructure are investigated for the misfitlayered Ca3Co4O9 and the complex perovskite-related Sr3RECo4O10.5 (RE = rare earth) cobalt-based oxides. For both systems, substitution of Ga for Co...... results in a simultaneous increase in the Seebeck coefficient (S) and the electrical conductivity (σ), and the influence is more significant in the high temperature region. The power factor (S 2 σ) is thereby remarkably improved by Ga substitution, particularly at high temperatures. Texture factor......0.05O9 shows the best ZT value of 0.45 at 1200 K, which is about 87.5% higher than the nondoped one, a considerable improvement....

Marine phytoplankton stoichiometry mediates nonlinear interactions between nutrient supply, temperature, and atmospheric CO2

Science.gov (United States)

Moreno, Allison R.; Hagstrom, George I.; Primeau, Francois W.; Levin, Simon A.; Martiny, Adam C.

2018-05-01

Marine phytoplankton stoichiometry links nutrient supply to marine carbon export. Deviations of phytoplankton stoichiometry from Redfield proportions (106C : 1P) could therefore have a significant impact on carbon cycling, and understanding which environmental factors drive these deviations may reveal new mechanisms regulating the carbon cycle. To explore the links between environmental conditions, stoichiometry, and carbon cycling, we compared four different models of phytoplankton C : P: a fixed Redfield model, a model with C : P given as a function of surface phosphorus concentration (P), a model with C P given as a function of temperature, and a new multi-environmental model that predicts C : P as a function of light, temperature, and P. These stoichiometric models were embedded into a five-box ocean circulation model, which resolves the three major ocean biomes (high-latitude, subtropical gyres, and tropical upwelling regions). Contrary to the expectation of a monotonic relationship between surface nutrient drawdown and carbon export, we found that lateral nutrient transport from lower C : P tropical waters to high C : P subtropical waters could cause carbon export to decrease with increased tropical nutrient utilization. It has been hypothesized that a positive feedback between temperature and pCO2, atm will play an important role in anthropogenic climate change, with changes in the biological pump playing at most a secondary role. Here we show that environmentally driven shifts in stoichiometry make the biological pump more influential, and may reverse the expected positive relationship between temperature and pCO2, atm. In the temperature-only model, changes in tropical temperature have more impact on the Δ pCO2, atm (˜ 41 ppm) compared to subtropical temperature changes (˜ 4.5 ppm). Our multi-environmental model predicted a decline in pCO2, atm of ˜ 46 ppm when temperature spanned a change of 10 °C. Thus, we find that variation in marine phytoplankton

Fabrication of magnetic alginate beads with uniform dispersion of CoFe{sub 2}O{sub 4} by the polydopamine surface functionalization for organic pollutants removal

Energy Technology Data Exchange (ETDEWEB)

Li, Xiaoli, E-mail: lixiaoli@lzu.edu.cn [Gansu Key Laboratory for Environmental Pollution Prediction and Control, College of Earth and Environmental Sciences, Lanzhou University, Lanzhou 730000 (China); Lu, Haijun, E-mail: 784616040@qq.com [Gansu Key Laboratory for Environmental Pollution Prediction and Control, College of Earth and Environmental Sciences, Lanzhou University, Lanzhou 730000 (China); Zhang, Yun, E-mail: zhangyun@lzu.edu.cn [Institute of Biochemical Engineering & Environmental Technology, College of Chemistry and Chemical Engineering, Lanzhou University, Lanzhou 730000 (China); He, Fu, E-mail: hef15@lzu.edu.cn [Institute of Biochemical Engineering & Environmental Technology, College of Chemistry and Chemical Engineering, Lanzhou University, Lanzhou 730000 (China); Jing, Lingyun, E-mail: jingly12@lzu.edu.cn [Gansu Key Laboratory for Environmental Pollution Prediction and Control, College of Earth and Environmental Sciences, Lanzhou University, Lanzhou 730000 (China); He, Xinghua, E-mail: 466410250@qq.com [Institute of Biochemical Engineering & Environmental Technology, College of Chemistry and Chemical Engineering, Lanzhou University, Lanzhou 730000 (China)

2016-12-15

Highlights: • SA@CoFe{sub 2}O{sub 4}-PDA with magnetic particles and biopolymers were used for dye removal. • SA@CoFe{sub 2}O{sub 4}-PDA exhibited the synergistic effect. • High adsorption capacities and fast kinetics were obtained. • Cationic dyes could be removed with high efficiency in a wide pH range. • Possible mechanism of adsorption was investigated. - Abstract: A simple and efficient method for production of magnetic composites by decorating CoFe{sub 2}O{sub 4} with polydopamine (PDA) through oxidative polymerization of dopamine was conducted. Further, magnetic alginate beads with porous structure containing well-dispersed CoFe{sub 2}O{sub 4}-PDA were fabricated by ionic crosslinking technology. The resulting SA@CoFe{sub 2}O{sub 4}-PDA beads were characterized using scanning electron microscopy, Fourier transform infrared spectrometry, X-ray diffractometer, vibrating sample magnetometer and X-ray photoelectron spectroscopy. Adsorption potential of SA@CoFe{sub 2}O{sub 4}-PDA beads for organic dyes including Methylene Blue (MB), Crystal Violet (CV) and Malachite Green (MG) was evaluated. SA@CoFe{sub 2}O{sub 4}-PDA beads exhibited excellent adsorption performances due to the composite effect, large surface area and porous structure. Organic dyes could be removed from water solution with high efficiency in a wide pH range of 4.0–9.0. Moreover, it exhibited much higher adsorptivity towards MB and CV with the maximum adsorption capacities of 466.60 and 456.52 mg/g, respectively, which were much higher than that of MG (248.78 mg/g). Ca-electrolyte had obvious adverse effects on MB and CV adsorption than MG. FTIR and XPS demonstrated that carboxylate, catechol, hydroxyl and amine groups might be involved in adsorption of organic dyes. The characteristics of wide pH range, high adsorption capacity and convenient magnetic separation would make SA@CoFe{sub 2}O{sub 4}-PDA beads as effective adsorbent for removal of organic dyes from wastewater.

Atmospheric carbon dioxide removal: long-term consequences and commitment

International Nuclear Information System (INIS)

Cao Long; Caldeira, Ken

2010-01-01

Carbon capture from ambient air has been proposed as a mitigation strategy to counteract anthropogenic climate change. We use an Earth system model to investigate the response of the coupled climate-carbon system to an instantaneous removal of all anthropogenic CO 2 from the atmosphere. In our extreme and idealized simulations, anthropogenic CO 2 emissions are halted and all anthropogenic CO 2 is removed from the atmosphere at year 2050 under the IPCC A2 CO 2 emission scenario when the model-simulated atmospheric CO 2 reaches 511 ppm and surface temperature reaches 1.8 deg. C above the pre-industrial level. In our simulations a one-time removal of all anthropogenic CO 2 in the atmosphere reduces surface air temperature by 0.8 deg. C within a few years, but 1 deg. C surface warming above pre-industrial levels lasts for several centuries. In other words, a one-time removal of 100% excess CO 2 from the atmosphere offsets less than 50% of the warming experienced at the time of removal. To maintain atmospheric CO 2 and temperature at low levels, not only does anthropogenic CO 2 in the atmosphere need to be removed, but anthropogenic CO 2 stored in the ocean and land needs to be removed as well when it outgasses to the atmosphere. In our simulation to maintain atmospheric CO 2 concentrations at pre-industrial levels for centuries, an additional amount of CO 2 equal to the original CO 2 captured would need to be removed over the subsequent 80 years.

The removal of gaseous impurities from the primary circuit in high temperature reactors with cerium-mischmetal-getters

International Nuclear Information System (INIS)

Heinen, R.

1986-11-01

The use of getters to remove tritium and other gaseous impurities (especially H 2 , N 2 and CO) from helium circuits in nuclear reactors has been investigated. The loading capcity of beds, containing small cerium-mischmetal chips has been tested for several typical conditions. The results show that it is possible to use getters to purify inert gas streams for given boundary conditions. High CO-levels, however, lead to a poisoning (passivation) of the getter material. The effect of poisoning is cumulative. A mathematical model describes the behavior of CO in this kind of getter. Safety tests under possible accident conditions were made with the highly reactive cerium-mischmetal chips. The results show that there isn't a critical problem in using this material in the form of a chemical reactive getter bed near a nuclear reactor in the investigated range of accident conditions. (orig.) [de

Elevated temperature and CO{sub 2} concentration effects on xylem anatomy of Scots pine

Energy Technology Data Exchange (ETDEWEB)

Kilpelainen, A.; Gerendiain, A.Z.; Luostarinen, K.; Peltola, H.; Kellomaki, S. [Joensuu Univ., Joensuu (Finland). Faculty of Forestry

2007-09-15

The effects of carbon dioxide (CO{sub 2}) concentrations and elevated temperatures on the xylem anatomy of 20-year old Scots pine trees were investigated. The experiment was conducted in 16 chambers containing 4 trees each with a factorial combination of both ambient and elevated CO{sub 2} concentrations and 2 different temperature regimes. CO{sub 2} concentrations were doubled with a corresponding increase of between 2 and 6 degrees C according to each season over a period of 6 years. The study showed that elevated CO{sub 2} concentrations increased the ring width in 4 of the 6 analyzed treatment years. Earlywood width increased during the first 2 years of the experiment, while latewood width increased during the third year of the study. The study also showed that the tracheid walls in both the latewood and earlywood samples were thicker when either temperature levels or CO{sub 2} levels were increased. It was noted that combined CO{sub 2} and temperature elevations resulted in thinner tracheid walls. However, latewood tracheid lumen diameters were larger in all CO{sub 2} and temperature treatments than trees grown in ambient conditions. It was concluded that xylem anatomy was impacted more by increases in temperature than by elevated CO{sub 2} concentrations. 48 refs., 2 tabs., 6 figs.

The effects of CO2 and nutrient fertilisation on the growth and temperature response of the mangrove Avicennia germinans.

Science.gov (United States)

Reef, Ruth; Slot, Martijn; Motro, Uzi; Motro, Michal; Motro, Yoav; Adame, Maria F; Garcia, Milton; Aranda, Jorge; Lovelock, Catherine E; Winter, Klaus

2016-08-01

In order to understand plant responses to both the widespread phenomenon of increased nutrient inputs to coastal zones and the concurrent rise in atmospheric CO2 concentrations, CO2-nutrient interactions need to be considered. In addition to its potential stimulating effect on photosynthesis and growth, elevated CO2 affects the temperature response of photosynthesis. The scarcity of experiments testing how elevated CO2 affects the temperature response of tropical trees hinders our ability to model future primary productivity. In a glasshouse study, we examined the effects of elevated CO2 (800 ppm) and nutrient availability on seedlings of the widespread mangrove Avicennia germinans. We assessed photosynthetic performance, the temperature response of photosynthesis, seedling growth and biomass allocation. We found large synergistic gains in both growth (42 %) and photosynthesis (115 %) when seedlings grown under elevated CO2 were supplied with elevated nutrient concentrations relative to their ambient growing conditions. Growth was significantly enhanced under elevated CO2 only under high-nutrient conditions, mainly in above-ground tissues. Under low-nutrient conditions and elevated CO2, root volume was more than double that of seedlings grown under ambient CO2 levels. Elevated CO2 significantly increased the temperature optimum for photosynthesis by ca. 4 °C. Rising CO2 concentrations are likely to have a significant positive effect on the growth rate of A. germinans over the next century, especially in areas where nutrient availability is high.

DEVELOPMENT OF DISPOSABLE SORBENTS FOR CHLORIDE REMOVAL FROM HIGH TEMPERATURE COAL-DERIVED GASES

Energy Technology Data Exchange (ETDEWEB)

Gopala Krishnan; Raghubir Gupta

1999-09-01

Advanced integrated-gasification combined-cycle (IGCC) and integrated-gasification fuel cell (IGFC) systems require the development of high temperature sorbents for the removal of hydrogen chloride (HCl) vapor to less than 1 parts-per-million (ppm) levels. HCl is a highly reactive, corrosive, and toxic gas which must be removed to meet environmental regulations, to protect power generation equipment, and to minimize deterioration of hot gas desulfurization sorbents. The objective of this program was to develop disposable, alkali-based sorbents capable of reducing HCl vapor levels to less than 1 ppm in the temperature range from 400 to 750 C and pressures in the range from 1 to 20 atm. The primary areas of focus of this program were to investigate different methods of sorbent fabrication, testing their suitability for different reactor configurations, obtaining reaction kinetics data, and conducting a preliminary economic feasibility assessment. This program was a joint effort between SRI International (SRI), Research Triangle Institute (RTI), and General Electric Corporate Research and Development (GE-CRD). SRI, the prime contractor and RTI, a major subcontractor, performed most of the work in this program. Thermochemical calculations indicated that sodium-based sorbents were capable of reducing HCl vapor levels to less than 1 ppm at temperatures up to 650 C, but the regeneration of spent sorbents would require complex process steps. Nahcolite (NaHCO{sub 3}), a naturally-occurring mineral, could be used as an inexpensive sorbent to remove HCl vapor in hot coal gas streams. In the current program, nahcolite powder was used to fabricate pellets suitable for fixed-bed reactors and granules suitable for fluidized-bed reactors. Pilot-scale equipment were used to prepare sorbents in large batches: pellets by disk pelletization and extrusion techniques, and granules by granulation and spray-drying techniques. Bench-scale fixed- and fluidized-bed reactors were assembled at

Analysis of a New Liquefaction Combined with Desublimation System for CO2 Separation Based on N2/CO2 Phase Equilibrium

Directory of Open Access Journals (Sweden)

Wenchao Yang

2015-09-01

Full Text Available Cryogenic CO2 capture is considered as a promising CO2 capture method due to its energy saving and environmental friendliness. The phase equilibrium analysis of CO2-mixtures at low temperature is crucial for the design and operation of a cryogenic system because it plays an important role in analysis of recovery and purity of the captured CO2. After removal of water and toxic gas, the main components in typical boiler gases are N2/CO2. Therefore, this paper evaluates the reliabilities of different cubic equations of state (EOS and mixing rules for N2/CO2. The results show that Peng-Robinson (PR and Soave-Redlich-Kwong (SRK fit the experimental data well, PR combined with the van der Waals (vdW mixing rule is more accurate than the other models. With temperature decrease, the accuracy of the model improves and the deviation of the N2 vapor fraction is 0.43% at 220 K. Based on the selected calculation model, the thermodynamic properties of N2/CO2 at low temperature are analyzed. According to the results, a new liquefaction combined with a desublimation system is proposed. The total recovery and purity of CO2 production of the new system are satisfactory enough for engineering applications. Additionally, the total energy required by the new system to capture the CO2 is about 3.108 MJ·kg−1 CO2, which appears to be at least 9% lower than desublimation separation when the initial concentration of CO2 is 40%.

Large-scale CO2 injection demos for the development of monitoring and verification technology and guidelines (CO2ReMoVe)

Energy Technology Data Exchange (ETDEWEB)

Wildenborg, T.; David, P. [TNO Built Environment and Geosciences, Princetonlaan 6, 3584 CB Utrecht (Netherlands); Bentham, M.; Chadwick, A.; Kirk, K. [British Geological Survey, Kingsley Dunham Centre, Keyworth, Nottingham NG12 5GG (United Kingdom); Dillen, M. [SINTEF Petroleum Research, Trondheim (Norway); Groenenberg, H. [Unit Policy Studies, Energy Research Centre of the Netherlands ECN, Amsterdam (Netherlands); Deflandre, J.P.; Le Gallo, J. [Institut Francais du Petrole, Rueil-Malmaison (France)

2009-04-15

The objectives of the EU project CO2ReMoVe are to undertake the research and development necessary to establish scientifically based standards for monitoring future CCS operations and to develop the performance assessment methodologies necessary to demonstrate the long-term reliability of geological storage of CO2. This could in turn lead to guidelines for the certification of sites suitable for CCS on a wide scale. Crucial to the project portfolio are the continuing large-scale CO2 injection operation at Sleipner, the injection operation at In Salah (Algeria) and the recently started injection project at Snoehvit (Norway). Two pilot sites are also currently in the project portfolio, Ketzin in Germany and K12-B in the offshore continental shelf of the Netherlands.

High temperature deformation of polycrystalline NiO and CoO

International Nuclear Information System (INIS)

Krishnamachari, V.; Notis, M.R.

1977-01-01

High temperature creep of polycrystalline NiO appears to be controlled by oxygen lattice diffusion at temperatures between 1273 and 1373 K and at stress levels from 34.5 to 79.8 MPa (5 to 11 ksi). Experimentally observed creep rates agree well with predictions obtained from deformation maps based on self-diffusion data. TEM examination indicates that dislocations present in crept NiO specimens are predominantly glide-type rather than climb-type dislocations as found in CoO. The difference in creep behavior of these materials is believed to be due to the difference in stacking fault energies and the nature of charge associated with lattice defects. 2 tables. 7 figs., 34 references

Mg/Ca- Δ CO3porewater2- -temperature calibration for Globobulimina spp.: A sensitive paleothermometer for deep-sea temperature reconstruction

Science.gov (United States)

Weldeab, Syee; Arce, Adam; Kasten, Sabine

2016-03-01

Existing benthic foraminiferal Mg/Ca-temperature calibrations are surrounded by substantial uncertainties mainly due to low temperature sensitivity of Mg/Ca in most benthic foraminifers and the effect of carbonate ion concentration on benthic foraminiferal Mg/Ca. Here we present Mg/Ca analysis of Rose Bengal stained and exceptionally well-preserved tests of the infaunal benthic foraminifer Globobulimina spp. from 39 eastern equatorial Atlantic core top samples. Mg/Ca in Globobulimina spp. varies between 2.5 mmol/mol and 9.1 mmol/mol corresponding to bottom water temperatures (BWT) between 1.8 °C and 19.1 °C and Δ CO3pore water2- between 33.7 ± 4 and - 34.3 ± 4 μmol /kg in sediment depths between 1 and 10 cm. Mg/Ca and BWT are linearly correlated with a best fit of Mg/Ca [mmol/mol] = (0.36 ± 0.02) * BWT [°C] + 2.22 ± 0.19 (r2 = 0.92, p-value: 11 *10-20, and n = 39). Using total alkalinity and pH data of pore water samples from 64 Atlantic multi-corer sites, we obtained Δ CO3pore water2- data from the depth habitat range of Globobulimina spp. (≥1 cm ≤ 10 cm below sediment surface). We show that Δ CO3pore waterSUP>2- is significantly lower than and linearly co-varies with the ΔCO2-3 of the overlying bottom water: Δ CO3pore water2- = (0.67 ± 0.05) * Δ CO3bottom water2- - (39.84 ± 1.98); r2 = 0.75, p-value: 6 *10-20, n = 64. We found a Mg/Ca sensitivity of 0.009 ± 0.0044 mmol /mol per μmol/kg Δ CO3pore water2- and Mg/Ca temperature sensitivity of 0.32 ± 0.06 mmol /mol / °C after a correction for the Δ CO3pore water2- effect. This study provides a robust Mg/Ca-temperature calibration, highlights that Δ CO3pore water2- is spatially and most likely temporally variable, and contradicts the notion that infaunal foraminiferal Mg/Ca is relatively immune from ΔCO2-3 changes in the overlying bottom water. Furthermore, comparison of down core Mg/Ca data of Cibicides pachyderma and Globobulimina spp. demonstrates that the high temperature sensitivity of

Meta-analysis of warmed versus standard temperature CO2 insufflation for laparoscopic cholecystectomy.

Science.gov (United States)

Hakeem, Abdul R; Birks, Theodore; Azeem, Qasim; Di Franco, Filippo; Gergely, Szabolcs; Harris, Adrian M

2016-06-01

There is conflicting evidence for the use of warmed, humidified carbon dioxide (CO2) for creating pneumoperitoneum during laparoscopic cholecystectomy. Few studies have reported less post-operative pain and analgesic requirement when warmed CO2 was used. This systematic review and meta-analysis aims to analyse the literature on the use of warmed CO2 in comparison to standard temperature CO2 during laparoscopic cholecystectomy. Systematic review and meta-analysis carried out in line with the PRISMA guidelines. Primary outcomes of interest were post-operative pain at 6 h, day 1 and day 2 following laparoscopic cholecystectomy. Secondary outcomes were analgesic usage and drop in intra-operative core body temperature. Standard Mean Difference (SMD) was calculated for continuous variables. Six randomised controlled trials (RCTs) met the inclusion criteria (n = 369). There was no significant difference in post-operative pain at 6 h [3 RCTs; SMD = -0.66 (-1.33, 0.02) (Z = 1.89) (P = 0.06)], day 1 [4 RCTs; SMD = -0.51 (-1.47, 0.44) (Z = 1.05) (P = 0.29)] and day 2 [2 RCTs; SMD = -0.96 (-2.30, 0.37) (Z = 1.42) (P = 0.16)] between the warmed CO2 and standard CO2 group. There was no difference in analgesic usage between the two groups, but pooled analysis was not possible. Two RCTs reported significant drop in intra-operative core body temperature, but there were no adverse events related to this. This review showed no difference in post-operative pain and analgesic requirements between the warmed and standard CO2 insufflation during laparoscopic cholecystectomy. Currently there is not enough high quality evidence to suggest routine usage of warmed CO2 for creating pneumoperitoneum during laparoscopic cholecystectomy. Copyright © 2015 Royal College of Surgeons of Edinburgh (Scottish charity number SC005317) and Royal College of Surgeons in Ireland. Published by Elsevier Ltd. All rights reserved.

Low temperature and short-term high-CO2 treatment in postharvest storage of table grapes at two maturity stages: Effects on transcriptome profiling.

Directory of Open Access Journals (Sweden)

Raquel Rosales

2016-07-01

Full Text Available Table grapes (Vitis vinifera cv. Cardinal are highly perishable and their quality deteriorates during postharvest storage at low temperature mainly because of sensitivity to fungal decay and senescence of rachis. The application of a 3-day CO2 treatment (20 kPa CO2 + 20 kPa O2 + 60 kPa N2 at 0ºC reduced total decay and retained fruit quality in early and late-harvested table grapes during postharvest storage. In order to study the transcriptional responsiveness of table grapes to low temperature and high CO2 levels in the first stage of storage and how the maturity stage affect these changes, we have performed a comparative large-scale transcriptional analysis using the custom-made GrapeGen GeneChip®. In the first stage of storage, low temperature led to a significantly intense change in grape skin transcriptome irrespective of fruit maturity, although there were different changes within each stage. In the case of CO2 treated samples, in comparison to fruit at time zero, only slight differences were observed. Functional enrichment analysis revealed that major modifications in the transcriptome profile of early- and late-harvested grapes stored at 0ºC are linked to biotic and abiotic stress-responsive terms. However, in both cases there is a specific reprogramming of the transcriptome during the first stage of storage at 0ºC in order to withstand the cold stress. Thus, genes involved in gluconeogenesis, photosynthesis, mRNA translation and lipid transport were up-regulated in the case of early-harvested grapes, and genes related to protein folding stability and intracellular membrane trafficking in late-harvested grapes. The beneficial effect of high CO2 treatment maintaining table grape quality seems to be an active process requiring the induction of several transcription factors and kinases in early-harvested grapes, and the activation of processes associated to the maintenance of energy in late-harvested grapes.

Low Temperature and Short-Term High-CO2 Treatment in Postharvest Storage of Table Grapes at Two Maturity Stages: Effects on Transcriptome Profiling.

Science.gov (United States)

Rosales, Raquel; Romero, Irene; Fernandez-Caballero, Carlos; Escribano, M Isabel; Merodio, Carmen; Sanchez-Ballesta, M Teresa

2016-01-01

Table grapes (Vitis vinifera cv. Cardinal) are highly perishable and their quality deteriorates during postharvest storage at low temperature mainly because of sensitivity to fungal decay and senescence of rachis. The application of a 3-day CO2 treatment (20 kPa CO2 + 20 kPa O2 + 60 kPa N2) at 0°C reduced total decay and retained fruit quality in early and late-harvested table grapes during postharvest storage. In order to study the transcriptional responsiveness of table grapes to low temperature and high CO2 levels in the first stage of storage and how the maturity stage affect these changes, we have performed a comparative large-scale transcriptional analysis using the custom-made GrapeGen GeneChip®. In the first stage of storage, low temperature led to a significantly intense change in grape skin transcriptome irrespective of fruit maturity, although there were different changes within each stage. In the case of CO2 treated samples, in comparison to fruit at time zero, only slight differences were observed. Functional enrichment analysis revealed that major modifications in the transcriptome profile of early- and late-harvested grapes stored at 0°C are linked to biotic and abiotic stress-responsive terms. However, in both cases there is a specific reprogramming of the transcriptome during the first stage of storage at 0°C in order to withstand the cold stress. Thus, genes involved in gluconeogenesis, photosynthesis, mRNA translation and lipid transport were up-regulated in the case of early-harvested grapes, and genes related to protein folding stability and intracellular membrane trafficking in late-harvested grapes. The beneficial effect of high CO2 treatment maintaining table grape quality seems to be an active process requiring the induction of several transcription factors and kinases in early-harvested grapes, and the activation of processes associated to the maintenance of energy in late-harvested grapes.

Functionalized dithiocarbamate chelating resin for the removal of Co2+ from simulated wastewater

Science.gov (United States)

Shi, Xuewei; Fu, Linwei; Wu, Yanyang; Zhao, Huiling; Zhao, Shuangliang; Xu, Shouhong

2017-12-01

Industrial wastewater that contains trace amounts of heavy metal ions is often seen in petrochemical industry. While this wastewater can not be directly discharged, it is difficult to treat due to the low concentration of metal ions. Introducing chelating reagents into this wastewater for selective ion adsorption, followed by a mechanical separation process, provides an appealing solution. Toward the success of this technology, the development of effective chelating resins is of key importance. In the present work, a chelating resin containing amino and dithiocarbamate groups was reported for the removal of Co(II) metal ions in trace concentrations from simulated wastewater. By investigating the adsorption performance of the chelating resin at different solution pH values, adsorbent dosages, contact time, initial ion concentrations, and adsorption temperatures, the maximum adsorption capacity of the resin for Co(II) was identified to be 24.89 mg g-1 for a 2 g L-1 adsorbent dosage and a pH value of 5. After four adsorption-desorption cycles, 97% of the adsorption capacity of the resin was maintained. The adsorption kinetics and thermodynamics were analyzed and discussed as well.

Chemical effects of a high CO2 concentration in oxy-fuel combustion of methane

DEFF Research Database (Denmark)

Glarborg, Peter; Bentzen, L.L.B.

2008-01-01

The oxidation of methane in an atmospheric-pres sure flow reactor has been studied experimentally under highly diluted conditions in N-2 and CO2, respectively. The stoichiometry was varied from fuel-lean to fuel-rich, and the temperatures covered the range 1200-1800 K. The results were interpreted...... CO2. The high local CO levels may have implications for near-burner corrosion and stagging, but increased problems with CO emission in oxy-fuel combustion are not anticipated....

Simultaneous removal of CO2 and H2S using MEA solution in a packed column absorber for biogas upgrading

Directory of Open Access Journals (Sweden)

Preecha Kasikamphaiboon

2013-12-01

Full Text Available Biogas production and utilization is an emerging alternative energy technology that has gained importance since the price of oil and gas has increased steadily over the last two decades. Biogas primarily consists of methane (CH4 and carbon dioxide (CO2 with smaller amounts of hydrogen sulfide (H2S and ammonia (NH3. For many applications the quality of biogas has to be improved. The main parameters that may require removal in upgrading systems are CO2 and H2S. This work presents the study of simultaneous absorption of CO2 and H2S by Monoethanolamine (MEA solution in a packed column. Simulated biogas containing 40% CO2 and 60% N2 and biogas generated from an anaerobic digestion plant were used as feed gas streams. The effects of gas flow rate, L/G ratio and absorbent concentration were investigated. The performance of the system was found to vary with process parameters. Increasing L/G ratio and MEA concentration causes the system efficiency to increase whereas increasing gas flow rate results in lower efficiency. An operating condition of L/G ratio of 83.3 ml/L, gas flow rate of 3 L/min and MEA concentration of 3 mol/L was found to remove more than 99.5% of CO2 and H2S from biogas. The volumetric overall mass-transfer coefficient (KGav for CO2 removal initially increases with increasing gas flow rate up to a certain value beyond which the coefficient becomes essentially constant. The KGav also increases with increasing L/G ratio throughout the range tested in this study.

Nitrous oxide flux under changing temperature and CO2

Science.gov (United States)

We are investigating nitrous oxide flux seasonal trends and response to temperature and CO2 increases in a boreal peatland. Peatlands located in boreal regions make up a third of global wetland area and are expected to have the highest temperature increases in response to climat...

Experimental Spectroscopic Studies of Carbon Monoxide (CO) Fluorescence at High Temperatures and Pressures.

Science.gov (United States)

Carrivain, Olivier; Orain, Mikael; Dorval, Nelly; Morin, Celine; Legros, Guillaume

2017-10-01

Two-photon excitation laser-induced fluorescence of carbon monoxide (CO-LIF) is investigated experimentally in order to determine the applicability of this technique for imaging CO concentration in aeronautical combustors. Experiments are carried out in a high temperature, high-pressure test cell, and in a laminar premixed CH 4 /air flame. Influence of temperature and pressure on CO-LIF spectra intensity and shape is reported. The experimental results show that as pressure increases, the CO-LIF excitation spectrum becomes asymmetric. Additionally, the spectrum strongly shifts to the red with a quadratic dependence of the collisional shift upon pressure, which is different from the classical behavior where the collisional shift is proportional to pressure. Moreover, pressure line broadening cannot be reproduced by a Lorenztian profile in the temperature range investigated here (300-1750 K) and, therefore, an alternative line shape is suggested.

High temperature reaction kinetics

International Nuclear Information System (INIS)

Jonah, C.D.; Beno, M.F.; Mulac, W.A.; Bartels, D.

1985-01-01

During the last year the dependence of the apparent rate of OD + CO on water pressure was measured at 305, 570, 865 and 1223 K. An explanation was found and tested for the H 2 O dependence of the apparent rate of OH(OD) + CO at high temperatures. The isotope effect for OH(D) with CO was determined over the temperature range 330 K to 1225 K. The reason for the water dependence of the rate of OH(OD) + CO near room temperatures has been investigated but no clear explanation has been found. 1 figure

Oysters and eelgrass: potential partners in a high pCO2 ocean.

Science.gov (United States)

Groner, Maya L; Burge, Colleen A; Cox, Ruth; Rivlin, Natalie; Turner, Mo; Van Alstyne, Kathryn L; Wyllie-Echeverria, Sandy; Bucci, John; Staudigel, Philip; Friedman, Carolyn S

2018-05-25

Climate change is affecting the health and physiology of marine organisms and altering species interactions. Ocean acidification (OA) threatens calcifying organisms such as the Pacific oyster, Crassostrea gigas. In contrast, seagrasses, such as the eelgrass Zostera marina, can benefit from the increase in available carbon for photosynthesis found at a lower seawater pH. Seagrasses can remove dissolved inorganic carbon from OA environments, creating local daytime pH refugia. Pacific oysters may improve the health of eelgrass by filtering out pathogens such as Labyrinthula zosterae (LZ), which causes eelgrass wasting disease (EWD). We examined how co-culture of eelgrass ramets and juvenile oysters affected the health and growth of eelgrass and the mass of oysters under different pCO 2 exposures. In Phase I, each species was cultured alone or in co-culture at 12°C across ambient, medium, and high pCO 2 conditions, (656, 1158 and1606 μatm pCO 2 , respectively). Under high pCO 2 , eelgrass grew faster and had less severe EWD (contracted in the field prior to the experiment). Co-culture with oysters also reduced the severity of EWD. While the presence of eelgrass decreased daytime pCO 2 , this reduction was not substantial enough to ameliorate the negative impact of high pCO 2 on oyster mass. In Phase II, eelgrass alone or oysters and eelgrass in co-culture were held at 15°C under ambient and high pCO 2 conditions, (488 and 2013 μatm pCO 2 , respectively). Half of the replicates were challenged with cultured LZ. Concentrations of defensive compounds in eelgrass (total phenolics and tannins), were altered by LZ exposure and pCO 2 treatments. Greater pathogen loads and increased EWD severity were detected in LZ exposed eelgrass ramets; EWD severity was reduced at high relative to low pCO 2 . Oyster presence did not influence pathogen load or EWD severity; high LZ concentrations in experimental treatments may have masked the effect of this treatment. Collectively, these

Perovskite Nanoparticle-Sensitized Ga2O3 Nanorod Arrays for CO Detection at High Temperature.

Science.gov (United States)

Lin, Hui-Jan; Baltrus, John P; Gao, Haiyong; Ding, Yong; Nam, Chang-Yong; Ohodnicki, Paul; Gao, Pu-Xian

2016-04-13

Noble metal nanoparticles are extensively used for sensitizing metal oxide chemical sensors through the catalytic spillover mechanism. However, due to earth-scarcity and high cost of noble metals, finding replacements presents a great economic benefit. Besides, high temperature and harsh environment sensor applications demand material stability under conditions approaching thermal and chemical stability limits of noble metals. In this study, we employed thermally stable perovskite-type La(0.8)Sr(0.2)FeO3 (LSFO) nanoparticle surface decoration on Ga2O3 nanorod array gas sensors and discovered an order of magnitude enhanced sensitivity to carbon monoxide at 500 °C. The LSFO nanoparticle catalysts was of comparable performance to that achieved by Pt nanoparticles, with a much lower weight loading than Pt. Detailed electron microscopy and X-ray photoelectron spectroscopy studies suggested the LSFO nanoparticle sensitization effect is attributed to a spillover-like effect associated with the gas-LSFO-Ga2O3 triple-interfaces that spread the negatively charged surface oxygen ions from LSFO nanoparticles surfaces over to β-Ga2O3 nanorod surfaces with faster surface CO oxidation reactions.

Low-Temperature Co-Fired Unipoled Multilayer Piezoelectric Transformers.

Science.gov (United States)

Gao, Xiangyu; Yan, Yongke; Carazo, Alfredo Vazquez; Dong, Shuxiang; Priya, Shashank

2018-03-01

The reliability of piezoelectric transformers (PTs) is dependent upon the quality of fabrication technique as any heterogeneity, prestress, or misalignment can lead to spurious response. In this paper, unipoled multilayer PTs were investigated focusing on high-power composition and co-firing profile in order to provide low-temperature synthesized high-quality device measured in terms of efficiency and power density. The addition of 0.2 wt% CuO into Pb 0.98 Sr 0.02 (Mg 1/3 Nb 2/3 ) 0.06 (Mn 1/3 Nb 2/3 ) 0.06 (Zr 0.48 Ti 0.52 ) 0.88 O 3 (PMMnN-PZT) reduces the co-firing temperature from 1240 °C to 930 °C, which allows the use of Ag/Pd inner electrode instead of noble Pt inner electrode. Low-temperature synthesized material was found to exhibit excellent piezoelectric properties ( , , %, pC/N, and °C). The performance of the PT co-fired with Ag/Pd electrode at 930 °C was similar to that co-fired at 1240 °C with Pt electrode (25% reduction in sintering temperature). Both high- and low-temperature synthesized PTs demonstrated 5-W output power with >90% efficiency and 11.5 W/cm 3 power density.

III. Co-electrodeposition/removal of copper and nickel in a spouted electrochemical reactor.

Science.gov (United States)

Grimshaw, Pengpeng; Calo, Joseph M; Hradil, George

2011-07-11

Results are presented of an investigation of co-electrodeposition of copper and nickel from acidic solution mixtures in a cylindrical spouted electrochemical reactor. The effects of solution pH, temperature, and applied current on metal removal/recovery rate, current efficiency, and corrosion of the deposited metals from the cathodic particles were examined under galvanostatic operation. The quantitative and qualitative behavior of co-electrodeposition of the two metals from their mixtures differs significantly from that of the individual single metal solutions. This is primarily attributed to the metal displacement reaction between Ni(0) and Cu(2+). This reaction effectively reduces copper corrosion, and amplifies that for nickel (at least at high concentrations). It also amplifies the separation of the deposition regimes of the two metals in time, which indicates that the recovery of each metal as a relatively pure deposit from the mixture is possible. It was also shown that nitrogen sparging considerably increases the observed net electrodeposition rates for both metals - considerably more so than from solutions with just the single metals alone. A numerical model of co-electrodeposition, corrosion, metal displacement, and mass transfer in the cylindrical spouted electrochemical reactor is presented that describes the behavior of the experimental copper and nickel removal data quite well.

Fabrication and thermoelectric properties of highly textured NaCo2O4 ceramic

International Nuclear Information System (INIS)

Cheng Jinguang; Sui Yu; Fu Haijin; Lu Zhe; Wei Bo; Qian Zhengnan; Miao Jipeng; Liu Zhiguo; Huang Xiqiang; Zhu Ruibin; Wang Xianjie; Su Wenhui

2006-01-01

Highly textured NaCo 2 O 4 polycrystalline sample was fabricated by means of the cold high-pressure compacting followed by the solid-state reaction. X-ray diffraction and scanning electron microscope were employed to show that the plate-like grains within the sample are aligned along the pressing direction. The resistivity ρ and thermoelectric power S along the preferred {0 0 1} plane were measured in the whole temperature range from 15 to 973 K in air and the correlation between thermoelectric properties and texture was investigated. It was found that both ρ and S exhibit metallic behavior in the whole temperature range and the above sample exhibits lower ρ and higher S due to high texture and density. The power factor exhibits a steep rise above 400 K and reaches 761 μW m -1 K -2 at 973 K, suggesting a promising candidate for thermoelectric application at higher temperature. The change of slope in both resistivity and thermoelectric power curves at about 450 K might arise from the spin-state transition of Co ions in the CoO 2 blocks

Li-promoted sodium zirconate as a CO{sub 2} absorbent at high temperatures; Zirconato de sodio promovido con Li como absorbente de CO{sub 2} a alta temperatura

Energy Technology Data Exchange (ETDEWEB)

Guzman Velderrain, V.; Barraza Jimenez, D.; Lardizabal Gutierrez, D.; Delgado Vigil, D.; Salinas Gutierrez, J.; Lopez Ortiz, A.; Collins-Martinez, V. [Centro de Investigacion en Materiales Avanzados S. C., Chihuahua, Chihuahua (Mexico)]. E-mail: virginia.collins@cimav.edu.mx

2009-09-15

In processes to produce hydrogen from fossil fuels, CO{sub 2} capture at high temperatures has played a crucial role in their conversion into energy-efficient processes. One example is steam reformer methane improved with absorption (SER), where CO{sub 2} capture at high temperatures (600 degrees Celsius) provides an energy savings of {approx_equal} 23% over conventional reformer processes (SMR). An important part of this concept is solid CO{sub 2} absorption, which must have adequate absorption capacity and rapid absorption/regeneration kinetics. Recently, synthetic CO{sub 2} absorbents have been developed that consist of mixed Li oxides. Previous studies conducted in our laboratory report that the absorption/regeneration properties of sodium zirconate (Na{sub 2}ZrO{sub 3}) are higher than Li-oxides. The objective of the present work is to increase the absorption capacity of Na{sub 2}ZrO{sub 3} at high temperatures without significantly affecting the kinetics of its absorption and regeneration, with Li promotion. The Na{sub 2}ZrO{sub 3} was synthesized by reaction in a solid state and impregnated with LiNO{sub 3} at different Li/Na ratios: 0, 0.03, 0.05, 0.1 and 0.25 (NZ, NZL3, NZL5, NZL10, NZL25). The characterization consisted of XRD and SEM. The evaluation as an absorbent was performed with TGA at 600 degrees Celsius in 80% CO{sub 2} (absorption) and 800 degrees Celsius in air (regeneration). While XRD shows only the Na{sub 2}ZrO{sub 3} structure in all the samples, the promoted samples present a signal shift with respect to Na{sub 2}ZrO{sub 3}, which is attributed to the substitution of Na atoms with Li. The TGA results indicate that the addition of Li to the Na{sub 2}ZrO{sub 3} structure does not significantly modify the absorption or regeneration kinetics. As the Li contents in the Na{sub 2}ZrO{sub 3} increase, the amount of CO{sub 2} capture increases up to a limit between 10 and 25% mol of Li. This is due to the displaced sodium presumably tending to form

Study on the adsorption of H2O and CO2 from the carrier gas of high-temperature gas-cooled reactor

International Nuclear Information System (INIS)

Liao Cuiping; Zheng Zhenhong; Shi Fuen; Zhou Dasen

1998-01-01

The author is focused on the experimental studies of the adsorption of moisture and carbon dioxide from the carrier gas of high-temperature gas-cooled reactor (HTGR). A suitable adsorbent--5A type molecular sieve spherical particles with an average diameter of 3 mm is chosen to purify the carrier gas with impurities of moisture and carbon dioxide. Experimental data at different concentration, flow rate, adsorptive temperature, pressure and bed depth are obtained from isothermal adsorption tests in order to examine the effects of these parameters on adsorption dynamic and for the optimal parameters selection of adsorption process. Experimental breakthrough curves, dynamic single component and multicomponent adsorption curves are obtained. The outlet concentration of H 2 O and CO 2 can reach below 1.0 x 10 -5 , so this purification system can meet the demands of HTGR

Effect of carbonation temperature on CO{sub 2} adsorption capacity of CaO derived from micro/nanostructured aragonite CaCO{sub 3}

Energy Technology Data Exchange (ETDEWEB)

Hlaing, Nwe Ni, E-mail: nwenihlaing76@gmail.com [School of Materials and Mineral Resources Engineering, Engineering Campus, Universiti Sains Malaysia, 14300 Nibong Tebal, Penang (Malaysia); Department of International Development Engineering, Tokyo Institute of Technology, 2-12-1 Ookayama, Meguro-ku, Tokyo (Japan); Department of Physics, University of Yangon, 11041 Kamayut, Yangon (Myanmar); Sreekantan, Srimala, E-mail: srimala@usm.my [School of Materials and Mineral Resources Engineering, Engineering Campus, Universiti Sains Malaysia, 14300 Nibong Tebal, Penang (Malaysia); Hinode, Hirofumi, E-mail: hinode@ide.titech.ac.jp; Kurniawan, Winarto, E-mail: Kurniawan.w.ab@m.titech.ac.jp [Department of International Development Engineering, Tokyo Institute of Technology, 2-12-1 Ookayama, Meguro-ku, Tokyo (Japan); Thant, Aye Aye, E-mail: a2thant@gmail.com [Department of Physics, University of Yangon, 11041 Kamayut, Yangon (Myanmar); Othman, Radzali, E-mail: radzali@utem.edu.my [Faculty of Manufacturing Engineering, Universiti Teknikal Malaysia Melaka, Hang Tuah Jaya, 76100 Durian Tunggal, Malacca (Malaysia); Mohamed, Abdul Rahman, E-mail: chrahman@eng.usm.my [Low Carbon Economy (LCE) Research Group, School of Chemical Engineering, Engineering Campus, Universiti Sains Malaysia, 14300 Nibong Tebal, Penang (Malaysia); Salime, Chris, E-mail: chris.salim@surya.ac.id [Environmental Engineering, Surya University, Tangerang, 15810 Banten (Indonesia)

2016-07-06

Recent years, CaO-based synthetic materials have been attracted attention as potential adsorbents for CO{sub 2} capture mainly due to their high CO{sub 2} adsorption capacity. In this study, micro/nanostructured aragonite CaCO{sub 3} was synthesized by a simple hydrothermal method with using polyacrylamide (PAM). The structural, morphological and thermal properties of the synthesized sample were investigated by X-ray diffraction (XRD), field-emission scanning electron microscopy (FESEM) and thermogravimetry analysis (TG-DTA). The XRD and FESEM results showed that the obtained sample was aragonite CaCO{sub 3} with aggregated nanorods and microspheres composed of nanorods. A TG-DTA apparatus with Thermoplus 2 software was used to investigate the effect of carbonation temperature on the CO{sub 2} adsorption capacity of CaO derived from aragonite CaCO{sub 3} sample. At 300 °C, the sample reached the CO{sub 2} adsorption capacity of 0.098 g-CO{sub 2}/g-adsorbent, whereas the sample achieved the highest capacity of 0.682 g-CO{sub 2}/g-adsorbent at 700 °C. The results showed that the carbonation temperature significantly influenced on the CO{sub 2} adsorption capacity of the CaO derived from aragonite CaCO{sub 3}.

Novel oral amphotericin B formulation (iCo-010) remains highly effective against murine systemic candidiasis following exposure to tropical temperature.

Science.gov (United States)

Wasan, Kishor M; Sivak, Olena; Bartlett, Karen; Wasan, Ellen K; Gershkovich, Pavel

2015-01-01

To evaluate the antifungal activity of amphotericin B (AmB) in a mouse model of systemic candidiasis following administration of a novel oral AmB formulation (iCo-010) that has been pre-exposed to tropical temperatures. Amphotericin B (AmB) was prepared as a 5 mg/mL dispersion in a mixture of Peceol, Gelucire 44/14 and VitE-TPGS 2,3 (iCo-010). The formulation was protected from light and incubated in a sealed container at 43 °C for 60 days. Mice infected with Candida albicans were treated with either iCo-010 formulation pre-incubated at 43 °C for 60 days or freshly prepared iCo-010 formulation at doses of 5, 10 and 20 mg/kg once daily for five consecutive days. Single intravenous 5 mg/kg dose of AmBisome® was used as a positive control group. Seven days following the last dose, the kidney, liver, spleen, lung, heart and brain were removed and the number of colony forming units (CFUs) was determined as a measure of tissue fungal load. In addition, the concentration of AmB within each tissue was determined using high performance liquid chromatography (HPLC). There were no significant differences in the reduction of CFUs and the concentration of AmB recovered in all organs at all iCo-010 doses tested between the freshly prepared iCo-010 formulation compared to the formulation that was incubated at 43 °C for 60 days. A novel oral AmB formulation, iCo-010, incubated at 43 °C for 60 days to simulate the exposure of the formulation to tropical temperatures remained highly effective against murine systemic candidiasis.

Deep Sea Memory of High Atmospheric CO2 Concentration

Science.gov (United States)

Mathesius, Sabine; Hofmann, Matthias; Caldeira, Ken; Schellnhuber, Hans Joachim

2015-04-01

Carbon dioxide removal (CDR) from the atmosphere has been proposed as a powerful measure to mitigate global warming and ocean acidification. Planetary-scale interventions of that kind are often portrayed as "last-resort strategies", which need to weigh in if humankind keeps on enhancing the climate-system stock of CO2. Yet even if CDR could restore atmospheric CO2 to substantially lower concentrations, would it really qualify to undo the critical impacts of past emissions? In the study presented here, we employed an Earth System Model of Intermediate Complexity (EMIC) to investigate how CDR might erase the emissions legacy in the marine environment, focusing on pH, temperature and dissolved oxygen. Against a background of a world following the RCP8.5 emissions path ("business-as-usual") for centuries, we simulated the effects of two massive CDR interventions with CO2 extraction rates of 5 GtC yr-1 and 25 GtC yr-1, respectively, starting in 2250. We found that the 5 GtC yr-1 scheme would have only minor ameliorative influence on the oceans, even after several centuries of application. By way of contrast, the extreme 25 GtC yr-1 scheme eventually leads to tangible improvements. However, even with such an aggressive measure, past CO2 emissions leave a substantial legacy in the marine environment within the simulated period (i.e., until 2700). In summary, our study demonstrates that anthropogenic alterations of the oceans, caused by continued business-as-usual emissions, may not be reversed on a multi-centennial time scale by the most aspirational geoengineering measures. We also found that a transition from the RCP8.5 state to the state of a strong mitigation scenario (RCP2.6) is not possible, even under the assumption of extreme extraction rates (25 GtC yr-1). This is explicitly demonstrated by simulating additional scenarios, starting CDR already in 2150 and operating until the atmospheric CO2 concentration reaches 280 ppm and 180 ppm, respectively. The simulated

Temperature dependence of differential conductance in Co-based Heusler alloy Co2TiSn and superconductor Pb junctions

Science.gov (United States)

Ooka, Ryutaro; Shigeta, Iduru; Umetsu, Rie Y.; Nomura, Akiko; Yubuta, Kunio; Yamauchi, Touru; Kanomata, Takeshi; Hiroi, Masahiko

2018-05-01

We investigated temperature dependence of differential conductance G (V) in planar junctions consisting of Co-based Heusler alloy Co2TiSn and superconductor Pb. Ferromagnetic Co2TiSn was predicted to be half-metal by first-principles band calculations. The spin polarization P of Co2TiSn was deduced to be 60.0% at 1.4 K by the Andreev reflection spectroscopy. The G (V) spectral shape was smeared gradually with increasing temperature and its structure was disappeared above the superconducting transition temperature Tc. Theoretical model analysis revealed that the superconducting energy gap Δ was 1.06 meV at 1.4 K and the Tc was 6.8 K , indicating that both values were suppressed from bulk values. However, the temperature dependent Δ (T) behavior was in good agreement with that of the Bardeen-Cooper-Schrieffer (BCS) theory. The experimental results exhibit that the superconductivity of Pb attached to half-metallic Co2TiSn was kept the conventional BCS mechanism characterized strong-coupling superconductors while its superconductivity was slightly suppressed by the superconducting proximity effect at the Co2TiSn/Pb interface.

High-pressure phase diagrams of liquid CO2 and N2

Science.gov (United States)

Boates, Brian; Bonev, Stanimir

2011-06-01

The phase diagrams of liquid CO2 and N2 have been investigated using first-principles theory. Both materials exhibit transitions to conducting liquids at high temperatures (T) and relatively modest pressures (P). Furthermore, both liquids undergo polymerization phase transitions at pressures comparable to their solid counterparts. The liquid phase diagrams have been divided into several regimes through a detailed analysis of changes in bonding, as well as structural and electronic properties for pressures and temperatures up to 200 GPa and 10 000 K, respectively. Similarities and differences between the high- P and T behavior of these fluids will be discussed. Calculations of the Hugoniot are in excellent agreement with available experimental data. Work supported by NSERC, LLNL, and the Killam Trusts. Prepared by LLNL under Contract DE-AC52-07NA27344.

Monolithic Au/CeO2 nanorod framework catalyst prepared by dealloying for low-temperature CO oxidation

Science.gov (United States)

Zhang, Xiaolong; Duan, Dong; Li, Guijing; Feng, Wenjie; Yang, Sen; Sun, Zhanbo

2018-03-01

Monolithic Au/CeO2 nanorod frameworks (NFs) with porous structure were prepared by dealloying melt-spun Al89.7Ce10Au0.3 ribbons. After calcination in O2, a 3D Au/CeO2 NF catalyst with large surface area was obtained and used for low-temperature CO oxidation. The small Au clusters/nanoparticles (NPs) were in situ supported and highly dispersed on the nanorod surface, creating many nanoscale contact interfaces. XPS results demonstrated that high-concentration oxygen vacancy and Au δ+/Au0 co-existed in the calcined sample. The Au/CeO2 nanorod catalyst calcined at 400 °C exhibited much higher catalytic activity for CO oxidation compared with the dealloyed sample and bare CeO2 nanorods. Moreover, its complete reaction temperature was as low as 91 °C. The designed Au/CeO2 NF catalyst not only possessed extreme sintering resistance but also exhibited high performance owing to the enhanced interaction between the Au clusters/NPs and CeO2 nanorod during calcination.

Formate-Dependent Microbial Conversion of CO2 and the Dominant Pathways of methanogenesis in production water of high-temperature oil reservoirs amended with bicarbonate

Directory of Open Access Journals (Sweden)

Guang-Chao eYang

2016-03-01

Full Text Available CO2 sequestration in deep-subsurface formations including oil reservoirs is a potential measure to reduce the CO2 concentration in the atmosphere. However, the fate of the CO2 and the ecological influences in Carbon Dioxide Capture and Storage (CDCS facilities is not understood clearly. In the current study, the fate of CO2 (in bicarbonate form (0~90 mM with 10 mM of formate as electron donor and carbon source was investigated with high-temperature production water from oilfield in China. The isotope data showed that bicarbonate could be reduced to methane by methanogens and major pathway of methanogenesis could be syntrophic formate oxidation coupled with CO2 reduction and formate methanogenesis under the anaerobic conditions. The bicarbonate addition induced the shift of microbial community. Addition of bicarbonate and formate was associated with a decrease of Methanosarcinales, but promotion of Methanobacteriales in all treatments. Thermodesulfovibrio was the major group in all the samples and Thermacetogenium dominated in the high bicarbonate treatments. The results indicated that CO2 from CDCS could be transformed to methane and the possibility of microbial CO2 conversion for enhanced microbial energy recovery in oil reservoirs.

Corrosion of high temperature alloys in the primary circuit helium of high temperature gas cooled reactors. Pt. 2

International Nuclear Information System (INIS)

Quadakkers, W.J.

1985-01-01

The reactive impurities H 2 O, CO, H 2 and CH 4 which are present in the primary coolant helium of high temperature gas-cooled reactors can cause scale formation, internal oxidation and carburization or decarburization of the high temperature structural alloys. In Part 1 of this contribution a theoretical model was presented, which allows the explanation and prediction of the observed corrosion effects. The model is based on a classical stability diagram for chromium, modified to account for deviations from equilibrium conditions caused by kinetic factors. In this paper it is shown how a stability diagram for a commercial alloy can be constructed and how this can be used to correlate the corrosion results with the main experimental parameters, temperature, gas and alloy composition. Using the theoretical model and the presented experimental results, conditions are derived under which a protective chromia based surface scale will be formed which prevents a rapid transfer of carbon between alloy and gas atmosphere. It is shown that this protective surface oxide can only be formed if the carbon monoxide pressure in the gas exceeds a critical value. Psub(CO), which depends on temperature and alloy composition. Additions of methane only have a limited effect provided that the methane/water ratio is not near to, or greater than, a critical value of around 100/1. The influence of minor alloying additions of strong oxide forming elements, commonly present in high temperature alloys, on the protective properties of the chromia surface scales and the kinetics of carbon transfer is illustrated. (orig.) [de

Design and Control of High Temperature PEM Fuel Cell Systems using Methanol Reformers with Air or Liquid Heat Integration

DEFF Research Database (Denmark)

Andreasen, Søren Juhl; Kær, Søren Knudsen; Sahlin, Simon Lennart

2013-01-01

The present work describes the ongoing development of high temperature PEM fuel cell systems fuelled by steam reformed methanol. Various fuel cell system solutions exist, they mainly differ depending on the desired fuel used. High temperature PEM (HTPEM) fuel cells offer the possibility of using...... methanol is converted to a hydrogen rich gas with CO2 trace amounts of CO, the increased operating temperatures allow the fuel cell to tolerate much higher CO concentrations than Nafion-based membranes. The increased tolerance to CO also enables the use of reformer systems with less hydrogen cleaning steps...... liquid fuels such as methanol, due to the increased robustness of operating at higher temperatures (160-180oC). Using liquid fuels such as methanol removes the high volume demands of compressed hydrogen storages, simplifies refueling, and enables the use of existing fuel distribution systems. The liquid...

Light-Triggered CO2 Breathing Foam via Nonsurfactant High Internal Phase Emulsion.

Science.gov (United States)

Zhang, Shiming; Wang, Dingguan; Pan, Qianhao; Gui, Qinyuan; Liao, Shenglong; Wang, Yapei

2017-10-04

Solid materials for CO 2 capture and storage have attracted enormous attention for gaseous separation, environmental protection, and climate governance. However, their preparation and recovery meet the problems of high energy and financial cost. Herein, a controllable CO 2 capture and storage process is accomplished in an emulsion-templated polymer foam, in which CO 2 is breathed-in under dark and breathed-out under light illumination. Such a process is likely to become a relay of natural CO 2 capture by plants that on the contrary breathe out CO 2 at night. Recyclable CO 2 capture at room temperature and release under light irradiation guarantee its convenient and cost-effective regeneration in industry. Furthermore, CO 2 mixed with CH 4 is successfully separated through this reversible breathing in and out system, which offers great promise for CO 2 enrichment and practical methane purification.

Multi-species time-history measurements during high-temperature acetone and 2-butanone pyrolysis

KAUST Repository

Lam, Kingyiu; Ren, Wei; Pyun, Sunghyun; Farooq, Aamir; Davidson, David Frank; Hanson, Ronald Kenneth

2013-01-01

High-temperature acetone and 2-butanone pyrolysis studies were conducted behind reflected shock waves using five species time-history measurements (ketone, CO, CH3, CH4 and C2H4). Experimental conditions covered temperatures of 1100-1600 Kat 1.6 atm

Magnetostriction of some cubic rare earth-Co2 compounds in high magnetic fields

International Nuclear Information System (INIS)

Moral, A. del; Melville, D.

1975-01-01

Magnetostriction measurements have been carried out in the cubic Laves phase compounds DyCo 2 , HoCo 2 and ErCo 2 from 10 K to well above their respective Neel temperatures Tsub(N). Pulsed magnetic fields up to 15 T (150kOe) were applied. The observed magnetostrictions are very large (approximately 10 -3 ) being similar to those found in the RFe 2 compounds. The measurements confirm the extremely high anisotropy of these materials. At the highest fields the polycrystalline samples are still undergoing rotational magnetization processes. The expected values of the saturation magnetostriction at O K are similar in sign and magnitude to those found in the corresponding rare earth metals. This fact and the scaling of magnetostriction with rare earth sublattice magnetization indicates that the rare earth ion is the main source of the magnetostriction. The metamagnetic transition above Tsub(N) has been studied, the relation between critical field and temperature being nonlinear for HoCo 2 and ErCo 2 . The compounds are highly anisotropic above Tsub(N) and all the features indicate that the field-induced phases are likely to be ferrimagnetic. (author)

Temperature dependence of CO2-enhanced primary production in the European Arctic Ocean

KAUST Repository

Holding, J. M.

2015-08-31

The Arctic Ocean is warming at two to three times the global rate1 and is perceived to be a bellwether for ocean acidification2, 3. Increased CO2 concentrations are expected to have a fertilization effect on marine autotrophs4, and higher temperatures should lead to increased rates of planktonic primary production5. Yet, simultaneous assessment of warming and increased CO2 on primary production in the Arctic has not been conducted. Here we test the expectation that CO2-enhanced gross primary production (GPP) may be temperature dependent, using data from several oceanographic cruises and experiments from both spring and summer in the European sector of the Arctic Ocean. Results confirm that CO2 enhances GPP (by a factor of up to ten) over a range of 145–2,099 μatm; however, the greatest effects are observed only at lower temperatures and are constrained by nutrient and light availability to the spring period. The temperature dependence of CO2-enhanced primary production has significant implications for metabolic balance in a warmer, CO2-enriched Arctic Ocean in the future. In particular, it indicates that a twofold increase in primary production during the spring is likely in the Arctic.

Rapid and selective removal of composite from tooth surfaces with a 9.3 µm CO2 laser using spectral feedback.

Science.gov (United States)

Chan, Kenneth H; Hirasuna, Krista; Fried, Daniel

2011-09-01

Dental composite restorative materials are color matched to the tooth and are difficult to remove by mechanical means without excessive removal or damage to peripheral enamel and dentin. Lasers are ideally suited for selective ablation to minimize healthy tissue loss when replacing existing restorations, sealants, or removing composite adhesives such as residual composite left after debonding orthodontic brackets. In this study, a carbon dioxide laser operating at 9.3-µm with a pulse duration of 10-20-microsecond and a pulse repetition rate of ∼200 Hz was integrated with a galvanometer based scanner and used to selectively remove composite from tooth surfaces. Spectra of the plume emission were acquired after each laser pulse and used to differentiate between the ablation of dental enamel or composite. Microthermocouples were used to monitor the temperature rise in the pulp chamber during composite removal. The composite was placed on tooth buccal and occlusal surfaces and the carbon dioxide laser beam was scanned across the surface to selectively remove the composite without excessive damage to the underlying sound enamel. The residual composite and the damage to the underlying enamel was evaluated using optical microscopy. The laser was able to rapidly remove composite from tooth buccal and occlusal surfaces with minimal damage to the underlying sound enamel and without excessive heat accumulation in the tooth. This study demonstrated that composite can be selectively removed from tooth surfaces at clinically relevant rates using a CO(2) laser operating at 9.3-µm with high pulse repetition rates with minimal heat deposition and damage to the underlying enamel. Copyright © 2011 Wiley-Liss, Inc.

Water Recycling removal using temperature-sensitive hydronen

Energy Technology Data Exchange (ETDEWEB)

Rana B. Gupta

2002-10-30

The overall objective of this project was to study the proposed Water Recycling/Removal Using Temperature-Sensitive Hydrogels. The main element of this technology is the design of a suitable hydrogel that can perform needed water separation for pulp and paper industry. The specific topics studied are to answer following questions: (a) Can water be removed using hydrogel from large molecules such as lignin? (b) Can the rate of separation be made faster? (c) What are the molecular interactions with hydrogel surface? (d) Can a hydrogel be designed for a high ionic strength and high temperature? Summary of the specific results are given.

Temperature dependence of the photodissociation of CO2 from high vibrational levels: 205-230 nm imaging studies of CO(X1Σ+) and O(3P, 1D) products

Science.gov (United States)

Sutradhar, S.; Samanta, B. R.; Samanta, A. K.; Reisler, H.

2017-07-01

The 205-230 nm photodissociation of vibrationally excited CO2 at temperatures up to 1800 K was studied using Resonance Enhanced Multiphoton Ionization (REMPI) and time-sliced Velocity Map Imaging (VMI). CO2 molecules seeded in He were heated in an SiC tube attached to a pulsed valve and supersonically expanded to create a molecular beam of rotationally cooled but vibrationally hot CO2. Photodissociation was observed from vibrationally excited CO2 with internal energies up to about 20 000 cm-1, and CO(X1Σ+), O(3P), and O(1D) products were detected by REMPI. The large enhancement in the absorption cross section with increasing CO2 vibrational excitation made this investigation feasible. The internal energies of heated CO2 molecules that absorbed 230 nm radiation were estimated from the kinetic energy release (KER) distributions of CO(X1Σ+) products in v″ = 0. At 230 nm, CO2 needs to have at least 4000 cm-1 of rovibrational energy to absorb the UV radiation and produce CO(X1Σ+) + O(3P). CO2 internal energies in excess of 16 000 cm-1 were confirmed by observing O(1D) products. It is likely that initial absorption from levels with high bending excitation accesses both the A1B2 and B1A2 states, explaining the nearly isotropic angular distributions of the products. CO(X1Σ+) product internal energies were estimated from REMPI spectroscopy, and the KER distributions of the CO(X1Σ+), O(3P), and O(1D) products were obtained by VMI. The CO product internal energy distributions change with increasing CO2 temperature, suggesting that more than one dynamical pathway is involved when the internal energy of CO2 (and the corresponding available energy) increases. The KER distributions of O(1D) and O(3P) show broad internal energy distributions in the CO(X1Σ+) cofragment, extending up to the maximum allowed by energy but peaking at low KER values. Although not all the observations can be explained at this time, with the aid of available theoretical studies of CO2 VUV

Gas exchange, growth, and defense responses of invasive Alliaria petiolata (Brassicaceae) and native Geum vernum (Rosaceae) to elevated atmospheric CO2 and warm spring temperatures.

Science.gov (United States)

Anderson, Laurel J; Cipollini, Don

2013-08-01

Global increases in atmospheric CO2 and temperature may interact in complex ways to influence plant physiology and growth, particularly for species that grow in cool, early spring conditions in temperate forests. Plant species may also vary in their responses to environmental changes; fast-growing invasives may be more responsive to rising CO2 than natives and may increase production of allelopathic compounds under these conditions, altering species' competitive interactions. We examined growth and physiological responses of Alliaria petiolata, an allelopathic, invasive herb, and Geum vernum, a co-occurring native herb, to ambient and elevated spring temperatures and atmospheric CO2 conditions in a factorial growth chamber experiment. At 5 wk, leaves were larger at high temperature, and shoot biomass increased under elevated CO2 only at high temperature in both species. As temperatures gradually warmed to simulate seasonal progression, G. vernum became responsive to CO2 at both temperatures, whereas A. petiolata continued to respond to elevated CO2 only at high temperature. Elevated CO2 increased thickness and decreased nitrogen concentrations in leaves of both species. Alliaria petiolata showed photosynthetic downregulation at elevated CO2, whereas G. vernum photosynthesis increased at elevated temperature. Flavonoid and cyanide concentrations decreased significantly in A. petiolata leaves in the elevated CO2 and temperature treatment. Total glucosinolate concentrations and trypsin inhibitor activities did not vary among treatments. Future elevated spring temperatures and CO2 will interact to stimulate growth for A. petiolata and G. vernum, but there may be reduced allelochemical effects in A. petiolata.

Growth performance and survival of larval Atlantic herring, under the combined effects of elevated temperatures and CO2.

Directory of Open Access Journals (Sweden)

Michael Sswat

Full Text Available In the coming decades, environmental change like warming and acidification will affect life in the ocean. While data on single stressor effects on fish are accumulating rapidly, we still know relatively little about interactive effects of multiple drivers. Of particular concern in this context are the early life stages of fish, for which direct effects of increased CO2 on growth and development have been observed. Whether these effects are further modified by elevated temperature was investigated here for the larvae of Atlantic herring (Clupea harengus, a commercially important fish species. Over a period of 32 days, larval survival, growth in size and weight, and instantaneous growth rate were assessed in a crossed experimental design of two temperatures (10°C and 12°C with two CO2 levels (400 μatm and 900 μatm CO2 at food levels mimicking natural levels using natural prey. Elevated temperature alone led to increased swimming activity, as well as decreased survival and instantaneous growth rate (Gi. The comparatively high sensitivity to elevated temperature in this study may have been influenced by low food levels offered to the larvae. Larval size, Gi and swimming activity were not affected by CO2, indicating tolerance of this species to projected "end of the century" CO2 levels. A synergistic effect of elevated temperature and CO2 was found for larval weight, where no effect of elevated CO2 concentrations was detected in the 12°C treatment, but a negative CO2 effect was found in the 10°C treatment. Contrasting CO2 effects were found for survival between the two temperatures. Under ambient CO2 conditions survival was increased at 12°C compared to 10°C. In general, CO2 effects were minor and considered negligible compared to the effect of temperature under these mimicked natural food conditions. These findings emphasize the need to include biotic factors such as energy supply via prey availability in future studies on interactive

Carbonate mineral solubility at low temperatures in the Na-K-Mg-Ca-H-Cl-SO 4-OH-HCO 3-CO 3-CO 2-H 2O system

Science.gov (United States)

Marion, Giles M.

2001-06-01

Carbonate minerals have played an important role in the geochemical evolution of Earth, and may have also played an important role in the geochemical evolution of Mars and Europa. Several models have been published in recent years that describe chloride and sulfate mineral solubilities in concentrated brines using the Pitzer equations. Few of these models are parameterized for subzero temperatures, and those that are do not include carbonate chemistry. The objectives of this work are to estimate Pitzer-equation bicarbonate-carbonate parameters and carbonate mineral solubility products and to incorporate them into the FREZCHEM model to predict carbonate mineral solubilities in the Na-K-Mg-Ca-H-Cl-SO 4-OH-HCO 3-CO 3-CO 2-H 2O system at low temperatures (≤25°C) with a special focus on subzero temperatures. Most of the Pitzer-equation parameters and equilibrium constants are taken from the literature and extrapolated into the subzero temperature range. Solubility products for 14 sodium, potassium, magnesium, and calcium bicarbonate and carbonate minerals are included in the model. Most of the experimental data are at temperatures ≥ -8°C; only for the NaHCO 3-NaCl-H 2O and Na 2CO 3-NaCl-H 2O systems are there bicarbonate and carbonate data to temperatures as low as -21.6°C. In general, the fit of the model to the experimental data is good. For example, calculated eutectic temperatures and compositions for NaHCO 3, Na 2CO 3, and their mixtures with NaCl and Na 2SO 4 salts are in good agreement with experimental data to temperatures as low as -21.6°C. Application of the model to eight saline, alkaline carbonate waters give predicted pHs ranging from 9.2 to 10.2, in comparison with measured pHs that range from 8.7 to 10.2. The model suggests that the CaCO 3 mineral that precipitates during seawater freezing is probably calcite and not ikaite. The model demonstrates that a proposed salt assemblage for the icy surface of Europa consisting of highly hydrated MgSO 4

Studies on CO2 removal and reduction. CO2 taisaku kenkyu no genjo

Energy Technology Data Exchange (ETDEWEB)

Shindo, Y [National Institute of Materials and Chemical Research, Tsukuba (Japan)

1993-02-01

This paper summarizes study trends mainly in CO2 fixing processes. Underground CO2 storage is a most promising method because it can fix a huge amount of CO2 and has low effects on ecological systems. Storing CO2 in ocean includes such methods as storing it in deep oceans; storing it in deep ocean beds; dissolving it into sea water; neutralizing it with calcium carbonates; and precipitating it as dry ice. Japan, disposing CO2 in these ways, may create international problems. Separation of CO2 may use a chemical absorption process as a superior method. Other processes discussed include a physical adsorption method and a membrane separation method. A useful method for CO2 fixation using marine organisms is fixation using coral reefs. This process will require an overall study including circulation of phosphorus and nitrogen. Marine organisms may include planktons and algae. CO2 fixation using land plants may be able to fix one trillion and 8 hundred billion tons of CO2 as converted to carbon. This process would require forest protection, prevention of desertification, and tree planting. Discussions are being given also on improving power generation cycles, recovering CO2 from automotive exhausts, and backfilling carbons into ground by means of photosynthesis. 23 refs., 7 figs., 1 tab.

High temperature magnetic properties of Co(FeY){sub 2}O{sub 4} synthesized by combustion reaction

Energy Technology Data Exchange (ETDEWEB)

Alves, Thiago Eduardo Pereira, E-mail: thiago.ifgo@gmail.com [Instituto Federal de Educacao, Ciencia e Tecnologia de Goias (IFGO), Goiania (Brazil); Franco Junior, Adolfo [Universidade Federal de Goias (UFG), Goiania (Brazil)

2016-07-01

Full text: Cobalt ferrite is widely studied due to its interesting magnetic behavior at room temperature. However, many technical applications require temperatures that are above that. Thus, it is necessary to understand how some magnetic properties, such as saturation magnetization (Ms), remanent magnetization (Mr), and coercivity (Hc), may behave at high temperatures [1]. Among several methods to synthesize cobalt ferrites, combustion reaction method is intensively used because it is inexpensive, fast and has good control on the stoichiometry. This method is based on the chemistry of propellants and explosives [2]. Therefore, we have prepared a series of nanoparticles of CoFe{sub (2-x)}Y{sub x}O{sub 4}, with x ranging from 0.00 to 0.04, by combustion reaction method. The crystal structure and morphology were characterized by X-ray diffraction (XRD) using Rietveld refinement and transmission electron microscopy (TEM), respectively. Nanocrystalline particles structures in the typical phase of spinel were observed on diffractograms. Micrographies showed high crystalline powders for the particles and particles size within nanoscale range. The magnetic properties were measured by vibrating sample magnetometry (VSM) in broad range of temperature (300-850K). Saturation magnetization (Ms) decreases with Y doping increase, while Hc increases, being about 1.8 higher than the undoped sample. Furthermore, Curie temperature increases with Y doping increase. These magnetic properties were discussed in terms of the particle interactions induced by the thermal fluctuations, cation distribution, and ions exchange between yttrium and cobalt atoms in A-B sites in the cubic structure [3]. References: [1] A. Franco, Jr. and F. C. e Silva, Applied Physics Letters 96, 172505, (2010). 525 [2] S.R. Jain, et al, Combustion and flame 40, 71-79, (1981). [3] A. Franco Jr. et al. Journal of Alloys and Compounds 680, 198-205, (2016). (author)

Porous carbon from local coconut shell char by CO2 and H2O activation in the presence of K2CO3

Science.gov (United States)

Vi, Nguyen Ngoc Thuy; Truyen, Dang Hai; Trung, Bien Cong; An, Ngo Thanh; Van Dung, Nguyen; Long, Nguyen Quang

2017-09-01

Vietnamese coconut shell char was activated by steam and carbon dioxide at low temperatures with the presence of K2CO3 as a catalyst. The effects of process parameters on adsorption capability of the product including different ratio of impregnation of activation agents, activation temperature, activation time were investigated in this study. Iodine number, methylene blue adsorption capacity, specific surface area and pore size distribution were measured to assess the properties of the activated carbon. Accordingly, the porous carbon was applied for toluene removal by adsorption technology. Significant increases in specific surface area and the toluene adsorption capacity were observed when the coconut shell char was activated in CO2 flow at 720 °C for 150 minutes and the K2CO3/char weight ratio of 0.5.

Highly anisotropic SmCo{sub 5} nanoflakes by surfactant-assisted ball milling at low temperature

Energy Technology Data Exchange (ETDEWEB)

Liu, Lidong; Zhang, Songlin [Key Laboratory of Magnetic Materials and Devices, Ningbo Institute of Material Technology and Engineering, Chinese Academy of Science, Ningbo 315201 (China); Zhejiang Province Key Laboratory of Magnetic Materials and Application Technology, Ningbo Institute of Material Technology and Engineering, Chinese Academy of Science, Ningbo 315201 (China); Zhang, Jian, E-mail: zhangj@nimte.ac.cn [Key Laboratory of Magnetic Materials and Devices, Ningbo Institute of Material Technology and Engineering, Chinese Academy of Science, Ningbo 315201 (China); Zhejiang Province Key Laboratory of Magnetic Materials and Application Technology, Ningbo Institute of Material Technology and Engineering, Chinese Academy of Science, Ningbo 315201 (China); Ping Liu, J. [Department of Physics, University of Texas at Arlington, Arlington, TX 76019 (United States); Xia, Weixing; Du, Juan; Yan, Aru [Key Laboratory of Magnetic Materials and Devices, Ningbo Institute of Material Technology and Engineering, Chinese Academy of Science, Ningbo 315201 (China); Zhejiang Province Key Laboratory of Magnetic Materials and Application Technology, Ningbo Institute of Material Technology and Engineering, Chinese Academy of Science, Ningbo 315201 (China); Yi, Jianhong [Institute of Material Science and Engineering, Kunming University of Science and Technology, Kunming 650500 (China); Li, Wei; Guo, Zhaohui [Division of Functional Materials, Central Iron and Steel Research Institute, Beijing 100081 (China)

2015-01-15

Surfactant-assisted ball milling (SABM) has been shown to be a promising method for preparing rare earth-transition metal (RE-TM) nanoflakes and nanoparticles. In this work, we prepared SmCo{sub 5} nanoflakes by SABM at low temperature, and 2-methyl pentane and trioctylamine were specially selected as solvent and surfactant, respectively, due to their low melting points. The effects of milling temperature on the morphology, microstructure and magnetic performance of SmCo{sub 5} nanoflakes were investigated systematically. Comparing with the samples milled at room temperature, the SmCo{sub 5} nanoflakes prepared at low temperature displayed more homogeneous morphology and lower oxygen content. Remarkably, better crystallinity, better grain alignment and larger remanence ratio were shown in the samples milled at low temperature, which resulted from the distinct microstructure caused by low milling temperature. The differences in structural evolution between the SmCo{sub 5} nanoflakes milled at room temperature and low temperature, including the formation of nanocrystalline, grain boundary sliding, grain rotation, et al., were discussed. It was found that lowering the temperature of SABM was a powerful method for the fabrication of RE-TM nanoflakes, which showed better hard magnetic properties and lower oxygen content. This was important for the preparation of high-performance sintered magnets, bonded magnets and nanocomposite magnets. - Highlights: • We prepare SmCo{sub 5} nanoflakes by surfactant-assisted ball milling at low temperature. • Better grain alignment and higher remanence ratio are achieved. • The oxygen content is reduced by lowering the milling temperature. • A distinct microstructural evolution caused by low milling temperature is clarified.

Preparation and characterization of mesoporous TiO{sub 2}-sphere-supported Au-nanoparticle catalysts with high activity for CO oxidation at ambient temperature