WorldWideScience

Sample records for carbon compounds

  1. Heterocyclic compounds as carbonic anhydrase inhibitor.

    Science.gov (United States)

    Husain, Asif; Madhesia, Diwakar

    2012-12-01

    The carbonic anhydrases (CAs, EC 4.2.1.1) constitute interesting targets for the design of pharmacological agents useful in the treatment or prevention of a variety of disorders such as, glaucoma, acid-base disequilibria, epilepsy, and other neuromuscular diseases, altitude sickness, edema, and obesity. A quite new and unexpected application of the CA inhibitors (CAIs) is with regard to their potential use in the management (imaging and treatment) of hypoxic tumors. A series of sulfonamides, including some clinically used derivatives like acetazolamide, methazolamide, ethoxzolamide, dichlorophenamide, dorzolamide, brinzolamide, benzolamide, and sulpiride, or indisulam, a compound in clinical development as antitumor drug, as well as the sulfamate antiepileptic drug topiramate have been reported to inhibit various human carbonic anhydrase isozyme. Various heterocyclic sulfonamides have been reported in this review with their potency to inhibit different carbonic anhydrases isozymes. PMID:21981003

  2. Analysis of lunar samples for carbon compounds.

    Science.gov (United States)

    Kvenvolden, K. A.

    1971-01-01

    Description of one approach to the analysis for carbon compounds in lunar materials from the Apollo 11 mission. The sequential scheme followed generally accepted organic geochemical practices, but was unusual in its application to a single sample. The procedures of the scheme were designed to minimize handling of the solids and extracts or hydrolysates. The solid lunar sample was retained in all steps of the sequential analysis in the vessel in which it was originally placed. Centrifugation was used to separate solid and liquid phases after extraction or refluxing. Liquids were recovered from solids by decantation.

  3. Carbon compounds in the atmosphere and their chemical reactions

    OpenAIRE

    Martišová, Petra

    2013-01-01

    The essay dissert on compounds of carbon in the atmosphere and its reaction. The most important are carbon dioxide, carbon monoxide and methane. Included among important compounds of carbon are volatile organic substances, polycyclic aromatic hydrocarbon and dioxin. Carbon dioxide and methane representing greenhouse gases have also indispensable meaning. As they, together with water vapour, nitrogen monoxide and other gases are causing the major part of greenhouse effect. Primarily because of...

  4. Laser ablation of molecular carbon nitride compounds

    International Nuclear Information System (INIS)

    We present a method for the preparation of thin films on sapphire substrates of the carbon nitride precursors dicyandiamide (C2N4H4), melamine (C3N6H6), and melem (C6N10H6), using the femtosecond-pulsed laser deposition technique (femto-PLD) at different temperatures. The depositions were carried out under high vacuum with a femtosecond-pulsed laser. The focused laser beam is scanned on the surface of a rotating target consisting of the pelletized compounds. The resulting polycrystalline, opaque films were characterized by X-ray powder diffraction, infrared, Raman, and X-ray photoelectron spectroscopy, photoluminescence, SEM, and MALDI-TOF mass spectrometry measurements. The crystal structures and optical/spectroscopic results of the obtained rough films largely match those of the bulk materials

  5. Laser ablation of molecular carbon nitride compounds

    Energy Technology Data Exchange (ETDEWEB)

    Fischer, D., E-mail: d.fischer@fkf.mpg.de [Max Planck Institute for Solid State Research, Heisenbergstr. 1, 70569 Stuttgart (Germany); Schwinghammer, K. [Max Planck Institute for Solid State Research, Heisenbergstr. 1, 70569 Stuttgart (Germany); Department of Chemistry, University of Munich, LMU, Butenandtstr. 5-13, 81377 Munich (Germany); Nanosystems Initiative Munich (NIM) and Center for Nanoscience (CeNS), 80799 Munich (Germany); Sondermann, C. [Max Planck Institute for Solid State Research, Heisenbergstr. 1, 70569 Stuttgart (Germany); Department of Chemistry, University of Munich, LMU, Butenandtstr. 5-13, 81377 Munich (Germany); Lau, V.W.; Mannhart, J. [Max Planck Institute for Solid State Research, Heisenbergstr. 1, 70569 Stuttgart (Germany); Lotsch, B.V. [Max Planck Institute for Solid State Research, Heisenbergstr. 1, 70569 Stuttgart (Germany); Department of Chemistry, University of Munich, LMU, Butenandtstr. 5-13, 81377 Munich (Germany); Nanosystems Initiative Munich (NIM) and Center for Nanoscience (CeNS), 80799 Munich (Germany)

    2015-09-15

    We present a method for the preparation of thin films on sapphire substrates of the carbon nitride precursors dicyandiamide (C{sub 2}N{sub 4}H{sub 4}), melamine (C{sub 3}N{sub 6}H{sub 6}), and melem (C{sub 6}N{sub 10}H{sub 6}), using the femtosecond-pulsed laser deposition technique (femto-PLD) at different temperatures. The depositions were carried out under high vacuum with a femtosecond-pulsed laser. The focused laser beam is scanned on the surface of a rotating target consisting of the pelletized compounds. The resulting polycrystalline, opaque films were characterized by X-ray powder diffraction, infrared, Raman, and X-ray photoelectron spectroscopy, photoluminescence, SEM, and MALDI-TOF mass spectrometry measurements. The crystal structures and optical/spectroscopic results of the obtained rough films largely match those of the bulk materials.

  6. Carbon-Based Compounds and Exobiology

    Science.gov (United States)

    Kerridge, John; DesMarais, David; Khanna, R. K.; Mancinelli, Rocco; McDonald, Gene; diBrozollo, Fillipo Radicati; Wdowiak, Tom

    1996-01-01

    The Committee for Planetary and Lunar Explorations (COMPLEX) posed questions related to exobiological exploration of Mars and the possibility of a population of carbonaceous materials in cometary nuclei to be addressed by future space missions. The scientific objectives for such missions are translated into a series of measurements and/or observations to be performed by Martian landers. These are: (1) A detailed mineralogical, chemical, and textural assessment of rock diversity at a landing site; (2) Chemical characterization of the materials at a local site; (3) Abundance of Hydrogen at any accessible sites; (4) Identification of specific minerals that would be diagnostic of aqueous processes; (5) Textual examination of lithologies thought to be formed by aqueous activity; (6) Search for minerals that might have been produced as a result of biological processes; (7) Mapping the distribution, in three dimensions, of the oxidant(s) identified on the Martian surface by the Viking mission; (8) Definition of the local chemical environment; (9) Determination of stable-isotopic ratios for the biogenic elements in surface mineral deposits; (10) Quantitative analysis of organic (non-carbonate) carbon; (11) Elemental and isotopic composition of bulk organic material; (12) Search for specific organic compounds that would yield information about synthetic mechanisms, in the case of prebiotic evolution, and about possible bio-markers, in the case of extinct or extant life; (13) and Coring, sampling, and detection of entrained gases and cosmic-ray induced reaction products at the polar ice cap. A discussion of measurements and/or observations required for cometary landers is included as well.

  7. Volatile organic compound emissions in relation to plant carbon fixation and the terrestrial carbon budget

    OpenAIRE

    Kesselmeier, J.; P. Ciccioli; Kuhn, U.; Stefani, P.; Biesenthal, T.; Rottenberger, S.; Wolf, A.; Vitullo, M.; R. Valentini; Nobre, A.; Kabat, P.; Andreae, M.O.

    2002-01-01

    A substantial amount of carbon is emitted by terrestrial vegetation as biogenic volatile organic compounds (VOC), which contributes to the oxidative capacity of the atmosphere, to particle production and to the carbon cycle. With regard to the carbon budget of the terrestrial biosphere, a release of these carbon compounds is regarded as a loss of photosynthetically fixed carbon. The significance of this loss for the regional and global carbon cycles is controversial. We estimate the amount of...

  8. Carbon compound used in hydrogen storage

    International Nuclear Information System (INIS)

    In the present work it is studied the activated carbon of mineral origin for the sorption of hydrogen. The carbon decreased of particle size by means of the one alloyed mechanical. The time of mill was of 10 hours. The characterization one carries out by scanning electron microscopy and X-ray diffraction. The hydrogen sipped in the carbon material it was determined using the Thermal gravimetric method (TGA). The conditions of hydrogenation went at 10 atm of pressure and ambient temperature during 18 hours. They were also carried out absorption/desorption cycles of hydrogen in the same one system of thermal gravimetric analysis. The results showed percentages of sorption of 2% approximately in the cycles carried out in the system TGA and of 4.5% in weight of hydrogen at pressure of 10 atmospheres and ambient temperature during 18 hours. (Author)

  9. Light harvesting with non covalent carbon nanotube / porphyrin compounds.

    OpenAIRE

    Roquelet, Cyrielle; Langlois, Benjamin; Vialla, Fabien; Garrot, Damien; Lauret, Jean-Sébastien; Voisin, Christophe

    2013-01-01

    We present recent developments in the synthesis and in the functional study of non covalently bound porphyrin/carbon nanotube compounds. The issue of the chemical stability of non covalent compounds is tackled by means of micelle assisted chemistry. The non covalent functionalization allows to preserve the electronic integrity of the nanotubes that display bright NIR luminescence. In the same time, the coupling between the subunits is very strong and leads to e cient energy transfer and PL qu...

  10. Integrating Carbon Nanotubes into Microfluidic Chip for Separating Biochemical Compounds

    OpenAIRE

    Chen, Miaoxiang Max; Mogensen, Klaus Bo; BØGGILD, Peter; Kutter, Jörg Peter

    2012-01-01

    We present a new type of device to separate biochemical compounds wherein carbon nanotubes (CNTs) are integrated as chromatographic stationary phase. The CNTs were directly grown on the bottom of microfluidic channels on Si/SiO2 substrates by chemical vapor deposition (CVD). Acetylene was used as carbon source and Ni was employed as catalyst. For electrokinetic separations, higher electrical field strength is usually required; therefore, the CNTs were constructed in pillar-array-form by patte...

  11. Carbon dioxide capture by means of cyclic organic nitrogen compounds

    OpenAIRE

    García Abuín, Alicia

    2012-01-01

    The research work included in present PhD Thesis involves the research studies to capture carbon dioxide using different cyclic nitrogen organic compounds (glucosamine (GA), chitosan (C), alkyl-pyrrolidones, pyrrolidine (PYR) and piperidine (PIP). This investigation is based on the study of three experimental systems. Each of them has characteristics potentially suitable to achieve the aim of this work, that is to say, to improve the carbon dioxide capture process, which is pre...

  12. Carbon limitation reveals allocation priority to defense compounds in peppermint

    Science.gov (United States)

    Forkelova, Lenka; Unsicker, Sybille; Forkel, Matthias; Huang, Jianbei; Trumbore, Susan; Hartmann, Henrik

    2016-04-01

    Studies of carbon partitioning during insect or pathogen infestation reveal high carbon investment into induced chemical defenses to deter the biotic agent (Baldwin, 1998). However, little is known how carbon investment into chemical defenses changes under abiotic stress such as drought. Drought forces plants to close their stomata to prevent water loss through transpiration while decreasing the amount of assimilated carbon. Furthermore drought hampers carbohydrates translocation due to declining plant hydration and reduced phloem functioning (McDowell, 2011; Hartmann et al., 2013; Sevanto, 2014). Hence long lasting drought can force plants into carbon starvation. The aim of our study was to disentangle carbon allocation priorities between growth, maintenance metabolism, storage and production of defense compounds under carbon limiting conditions using peppermint as our model plant. Drought is not the only method how to manipulate plant carbon metabolism and photosynthetic yield. Exposing plants to reduced [CO2] air is a promising tool simulating drought induced carbon limitation without affecting phloem functioning and so carbohydrate translocation (Hartmann et al., 2015). We exposed peppermint plants to drought (50% of the control irrigation) and to low [CO2] (progressive decrease from 350 ppm to 20 ppm) to disentangle hydraulic failure from carbon starvation effects on carbon allocation. Drought was applied as a cross-treatment yielding four treatments: watered and high [CO2] (W+CO2), drought and high [CO2] (D+CO2), water and low [CO2] (W-CO2), drought and low [CO2] (D-CO2). We analyzed the most abundant terpenoid defense compounds (α-Pinene, sabinene, myrcene, limonene, menthone, menthol and pulegone) and used continuous 13CO2 labelling to trace allocation pattern of new and old assimilated carbon in the four carbon sinks (structural biomass, water soluble sugars, starch and terpenoid defense compounds) in young expanding leaf tissue. This leaf tissue grew

  13. Tracing carbon fixation in phytoplankton—compound specific and total

    NARCIS (Netherlands)

    Grosse, J.; Van Breugel, P.; Boschker, H.T.S.

    2015-01-01

    Measurement of total primary production using 13C incorporation is a widely established tool. However, these bulk measurements lack information about the fate of fixed carbon: the production of major cellular compounds (carbohydrates, amino acids, fatty acids, and DNA/RNA) is affected by for instanc

  14. Integrating Carbon Nanotubes into Microfluidic Chip for Separating Biochemical Compounds

    DEFF Research Database (Denmark)

    Chen, Miaoxiang Max; Mogensen, Klaus Bo; Bøggild, Peter;

    2012-01-01

    We present a new type of device to separate biochemical compounds wherein carbon nanotubes (CNTs) are integrated as chromatographic stationary phase. The CNTs were directly grown on the bottom of microfluidic channels on Si/SiO2 substrates by chemical vapor deposition (CVD). Acetylene was used as...

  15. Experimental investigation of single carbon compounds under hydrothermal conditions

    Science.gov (United States)

    Seewald, Jeffrey S.; Zolotov, Mikhail Yu.; McCollom, Thomas

    2006-01-01

    The speciation of carbon in subseafloor hydrothermal systems has direct implications for the maintenance of life in present-day vent ecosystems and possibly the origin of life on early Earth. Carbon monoxide is of particular interest because it represents a key reactant during the abiotic synthesis of reduced carbon compounds via Fischer-Tropsch-type processes. Laboratory experiments were conducted to constrain reactions that regulate the speciation of aqueous single carbon species under hydrothermal conditions and determine kinetic parameters for the oxidation of CO according to the water water-gas shift reaction (CO 2 + H 2 = CO + H 2O). Aqueous fluids containing added CO 2, CO, HCOOH, NaHCO 3, NaHCOO, and H 2 were heated at 150, 200, and 300 °C and 350 bar in flexible-cell hydrothermal apparatus, and the abundances of carbon compounds was monitored as a function of time. Variations in fluid chemistry suggest that the reduction of CO 2 to CH 3OH under aqueous conditions occurs via a stepwise process that involves the formation of HCOOH, CO, and possibly CH 2O, as reaction intermediaries. Kinetic barriers that inhibit the reduction of CH 3OH to CH 4 allow the accumulation of reaction intermediaries in solution at high concentrations regulated by metastable thermodynamic equilibrium. Reaction of CO 2 to CO involves a two-step process in which CO 2 initially undergoes a reduction step to HCOOH which subsequently dehydrates to form CO. Both reactions proceed readily in either direction. A preexponential factor of 1.35 × 10 6 s -1 and an activation energy of 102 kJ/mol were retrieved from the experimental results for the oxidation of CO to CO 2. Reaction rates amongst single carbon compounds during the experiments suggest that ΣCO 2 (CO 2 + HCO 3- + CO 32-), CO, ΣHCOOH (HCOOH + HCOO -), and CH 3OH may reach states of redox-dependent metastable thermodynamic equilibrium in subseafloor and other hydrothermal systems. The abundance of CO under equilibrium conditions

  16. Molecular switches in carbon-rich organometallic compounds: Theoretical aspects

    Energy Technology Data Exchange (ETDEWEB)

    Costuas, Karine, E-mail: kcostuas@univ-rennes1.fr [Sciences chimiques de Rennes, UMR 6226 CNRS - Université de Rennes 1, Avenue du Général Leclerc F-35042 Rennes (France)

    2015-01-22

    Organometallic complexes associated with an appropriate choice of ancillary ligands reveal to have a wide range of physical properties leading to promising applications when incorporated in nano-size devices. The challenge is to design innovative multifunctional compounds based on redox active carbon-rich organometallics associated with spin carriers and/or photochromic units. A multidisciplinary approach in this area has proved to be efficient in a series a systems combining carbon-rich bridging ligands and redox metallic moieties. In this domain, the role of theoretical investigations based on quantum mechanics tools have a crucial role in rationalizing and in helping designing systems possessing target properties.

  17. Molecular switches in carbon-rich organometallic compounds: Theoretical aspects

    International Nuclear Information System (INIS)

    Organometallic complexes associated with an appropriate choice of ancillary ligands reveal to have a wide range of physical properties leading to promising applications when incorporated in nano-size devices. The challenge is to design innovative multifunctional compounds based on redox active carbon-rich organometallics associated with spin carriers and/or photochromic units. A multidisciplinary approach in this area has proved to be efficient in a series a systems combining carbon-rich bridging ligands and redox metallic moieties. In this domain, the role of theoretical investigations based on quantum mechanics tools have a crucial role in rationalizing and in helping designing systems possessing target properties

  18. Irreversible adsorption of phenolic compounds by activated carbons

    International Nuclear Information System (INIS)

    Studies were undertaken to determine the reasons why phenolic sorbates can be difficult to remove and recover from activated carbons. The chemical properties of the sorbate and the adsorbent surface, and the influences of changes in the adsorption and desorption conditions were investigated. Comparison of isotherms established after different contact times or at different temperatures indicated that phenolic compounds react on carbon surfaces. The reaction rate is a strong function of temperature. Regeneration of carbons by leaching with acetone recovered at least as much phenol as did regeneration with other solvents or with displacers. The physiochemical properties of adsorbents influences irreversible uptakes. Sorbates differed markedly in their tendencies to undergo irreversible adsorption. 64 refs., 47 figs., 32 tabs

  19. Photoassisted carbon dioxide reduction and formation of twoand three-carbon compounds. [prebiological photosynthesis

    Science.gov (United States)

    Halmann, M.; Aurian-Blajeni, B.; Bloch, S.

    1981-01-01

    The photoassisted reduction of aqueous carbon dioxide in the presence of naturally occurring minerals is investigated as a possible abiotic precursor of photosynthesis. Aqueous carbon dioxide saturated suspensions or surfaces of the minerals nontronite, bentonite, anatase, wolframite, molybdenite, minium, cinnabar and hematite were irradiated with high-pressure mercury lamps or sunlight. Chemical analyses reveal the production of formic acid, formaldehyde, methanol and methane, and the two and three-carbon compounds glyoxal (CHOCHO) and malonaldehyde (CH2(CHO)2). It is suggested that such photosynthetic reactions with visible light in the presence of semiconducting minerals may provide models for prebiological carbon and nitrogen fixation in both oxidized and reduced atmospheres.

  20. Improved quality control of carbon-14 labelled compounds

    International Nuclear Information System (INIS)

    IUT Ltd is a producer of carbon-14 labelled organic compounds like benzene, methanol, phenol, formaldehyde, Na-acetates and also special ordered compounds. The quality control of these compounds is carried out by means of HPLC and GC-MS due to chemical purity. Molar activity was determined by Liquid Scintillation Counting and HPLC being equipped by a radioactivity detector. Unfortunately the accuracy of the activity determination was arrived only ±4% relatively. This error is too high because of the large dilution factors. In respect of the IUT accreditation as an analytical laboratory in Germany the accuracy had to be improved remarkably. Therefore the GC-MS-determination of molar activities of labelled compounds is used as the 14C-labelled compound. A special evaluation code is used to determine the enrichment values relative to the unlabelled molecules. Taking into account the results of GC-MS the accuracy of molar activity determination is improved to ±2%. The spectra evaluation is demonstrated and some examples are discussed

  1. Influence of sulfur compounds on the terrestrial carbon cycle

    Science.gov (United States)

    Eliseev, A. V.

    2015-11-01

    Using the climate model developed at the A.M. Obukhov Institute of Atmospheric Physics, Russian Academy of Sciences (IAP RAS CM), numerical experiments have been conducted in line with the Coupled Model Intercomparison Project Phase 5 (CMIP5), but scaling the anthropogenic emissions of sulfur compounds into the troposphere by ±25%. Two types of impacts of sulfur compounds on climate and the global carbon cycle are considered: climate impact (CI, associated with the influence of tropospheric sulfates on climate and, as a consequence, on the carbon cycle characteristics) and ecological impact (EI, associated with the influence of SO2 on the rate of photosynthesis of terrestrial plants). The climate impact was found to be generally more important than the ecological one. However, in a number of regions, the EI is comparable to CI, including in the southeast parts of North America and, especially, of Asia. The contribution of EI to the change in global characteristics of terrestrial ecosystems in the 20th century is likewise considerable. The CI is generally more sensitive to the uncertainty in anthropogenic emissions of sulfur compounds into the troposphere than the EI.

  2. Kirishites, a new type of natural high-carbon compounds

    Science.gov (United States)

    Marin, Yu. B.; Skublov, G. T.; Yushkin, N. P.

    2010-01-01

    On the right-hand bank of the Volkhov River, in the natural area of tektite-like glasses (Volkhovites), fragments of shungites and slags with bunches of hairlike dark brownish enclosures were found. The filament thickness ranged from 20 to 100 μm, and separate “hairlines” were 3 cm in length. The composition of shungites and “hairlines” was found to be identical, which allowed us to consider the latter as aposhungite carbon formations. The high-carbon hairline structures associated with volkhovites are called kirishites. Kirishites are a new type of high-carbon structures that formed simultaneously with volkhovites in the case of explosion-type delivery of carbon slag and shungite fragments to the daylight surface during Holocene explosive activity. Under sharply reductive conditions, the slags partially melted, the melts were segregated, and carbonaceous-silicate and carbonaceous-ferriferous glasses formed with subsequent decompression-explosive liberation of carbon-supersaturated structures, which were extruded from shungite and slag fragments in the form of a resinoid mass. The “hairlines” were found to be zonal in structure: the central axial zones are composed of high-nitrogen hydrocarbon compounds, and peripheral regions are essentially carbonaceous with a high content of organic-mineral compounds and numerous microanomalies of petrogenic, volatile, rare, and ore elements. Infrared spectroscopy identified in kirishites proteinlike compounds, diagnosed in absorption bands (in cm-1) 600-720 (Amid V), 1200-1300 (Amid III), 1480-1590 (Amid II), 1600-1700 (Amid I), 3000-3800 (vibrations in NH2 and II groups). Gas chromatography, with the possibility of differentiation of left- and right-handed forms, revealed a broad spectrum of amino acids in kirishites, with their total content found to be the absolutely highest record for natural bitumens, an order of magnitude higher than the largest amino acid concentrations ever revealed in fibrous high

  3. Selective Sorption of Dissolved Organic Carbon Compounds by Temperate Soils

    Energy Technology Data Exchange (ETDEWEB)

    Jagadamma, Sindhu [ORNL; Mayes, Melanie [ORNL; Phillips, Jana Randolph [ORNL

    2012-01-01

    Physico-chemical sorption of dissolved organic carbon (DOC) on soil minerals is one of the major processes of organic carbon (OC) stabilization in soils, especially in deeper layers. The attachment of C on soil solids is related to the reactivity of the soil minerals and the chemistry of the sorbate functional groups, but the sorption studies conducted without controlling microbial activity may overestimate the sorption potential of soil. This study was conducted to examine the sorptive characteristics of a diverse functional groups of simple OC compounds (D-glucose, L-alanine, oxalic acid, salicylic acid, and sinapyl alcohol) on temperate climate soil orders (Mollisols, Ultisols and Alfisols) with and without biological degradative processes. Equilibrium batch experiments were conducted using 0-100 mg C L-1 at a solid-solution ratio of 1:60 for 48 hrs and the sorption parameters were calculated by Langmuir model fitting. The amount of added compounds that remained in the solution phase was detected by high performance liquid chromatography (HPLC) and total organic C (TOC) analysis. Soil sterilization was performed by -irradiation technique and experiments were repeated to determine the contribution of microbial degradation to apparent sorption. Overall, Ultisols did not show a marked preference for apparent sorption of any of the model compounds, as indicated by a narrower range of maximum sorption capacity (Smax) of 173-527 mg kg soil-1 across compounds. Mollisols exhibited a strong preference for apparent sorption of oxalic acid (Smax of 5290 mg kg soil-1) and sinapyl alcohol (Smax of 2031 mg kg soil-1) over the other compounds. The propensity for sorption of oxalic acid is mainly attributed to the precipitation of insoluble Ca-oxalate due to the calcareous nature of most Mollisol subsoils and its preference for sinapyl alcohol could be linked to the polymerization of this lignin monomer on 2:2 mineral dominated soils. The reactivity of Alfisols to DOC was in

  4. Reactions between sodium and various carbon bearing compounds

    International Nuclear Information System (INIS)

    The presence of carbon bearing materials in liquid sodium is undesirable because of their ability to carburise stainless steel components. It has been demonstrated for example that carbon taken up by stainless steels can affect their mechanical properties and that thinner sectioned material such as fuel cladding and the tubing of intermediate heat exchanger may be more sensitive to such effects. Generally speaking, there are a number of potential carbon sources in reactor systems. Some of the sources such as the graphite in neutron shield rods, boron carbide in control rods and carbide fuels are part of the reactor designs while others such as oil in mechanical pumps arid 'coupling-fluids' used to inspect plant components are associated with the respective operation arid inspection of the plant. In this paper it is intended to discuss in general terms the way these various compounds behave in liquid sodium and to assess what effect their presence will have on the materials of construction in fast reactor systems. The paper also reviews the chemistry of the environment in relation to the types of carburizing species which may exist in sodium systems

  5. Hydrogenated 5-carbon compound and method of making

    Science.gov (United States)

    Elliott, Douglas C.; Frye, John G.

    1999-01-01

    The present invention is based upon the surprising discovery that a 5-carbon compound selected from the group of 4-oxopentanoic acid, at least one lactone of 4-oxopentanoic acid, and combinations thereof, may be hydrogenated with a bimetallic catalyst of a noble metal in combination with a second metal and preserve the pendant methyl group. It was further unexpectedly discovered that the same conditions of bimetallic catalyst in the presence of hydrogen are useful for catalyzing the different intermediate reactions for example angelicalactone to gamma-valerolactone and gamma-valerolactone to 1,4-pentanediol. Finally, it was surprising that levulinic acid could be converted to 2-methyltetrahydrofuran with heating in the presence of the bimetallic catalyst and hydrogen in a single process vessel. The method of the present invention unexpectedly produced a fuel or fuel component having 2-methyltetrahydrofuran either in a yield greater than 4.5 mol % or in combination with alcohols.

  6. Hydrogenated 5-carbon compound and method of making

    Energy Technology Data Exchange (ETDEWEB)

    Elliott, D.C.; Frye, J.G.

    1999-03-16

    The present invention is based upon the surprising discovery that a 5-carbon compound selected from the group of 4-oxopentanoic acid, at least one lactone of 4-oxopentanoic acid, and combinations thereof, may be hydrogenated with a bimetallic catalyst of a noble metal in combination with a second metal and preserve the pendant methyl group. It was further unexpectedly discovered that the same conditions of bimetallic catalyst in the presence of hydrogen are useful for catalyzing the different intermediate reactions, for example, angelicalactone to gamma-valerolactone and gamma-valerolactone to 1,4-pentanediol. Finally, it was surprising that levulinic acid could be converted to 2-methyltetrahydrofuran with heating in the presence of the bimetallic catalyst and hydrogen in a single process vessel. The method of the present invention unexpectedly produced a fuel or fuel component having 2-methyltetrahydrofuran either in a yield greater than 4.5 mol % or in combination with alcohols. 8 figs.

  7. Microtrapping of volatile organic compounds with carbon nanotubes

    Directory of Open Access Journals (Sweden)

    Chaudhery Mustansar Hussain

    2010-10-01

    Full Text Available Micro-sorbent traps referred to as microtraps serve as integrated concentration-injection devices for continuousmonitoring in gas phase streams. The application of carbon nanotubes as unique sorbents for the fabrication of microtrapsfor the nano-scale adsorption/desorption of volatile organic molecules is presented in this paper. The microtrap applicationrequires high adsorption capacity as well as easy desorbability; the latter being critical for injection mode of these integrateddevices. The micro-sorbent characteristics of single and multi-walled carbon nanotubes for gas phase adsorption/desorptionof several volatile organic compounds like DCM, ethanol and benzene etc. has been studied. The nonporous nature of carbonnanotubes (CNTs eliminates the mass transfer resistance related to diffusion into pore structures, thus allowing easydesorbability. At the same time, their high aspect ratios lead to large breakthrough volumes. As compared to a commercialsorbent carbopackTM, the breakthrough volume was as much as an order of magnitude higher in the CNTs, while the higherrate of desorption measured as the peak width at half height of the desorption band was found nearly eight times lower (i.e.,0.26 seconds with SWNT and 1.89 seconds with carbopackTM. The trapping and desorption characteristics of single andmulti walled nanotubes were found to be comparable. We also found that the presence of disordered carbon impurities,which could be removed by controlled oxidative annealing, could greatly degrade the performance of CNTs. This researchhas suggested that CNTs can be used in micro-sorbent traps and surprisingly enhance the efficiency of the integrated concentration-injection devices. Consequently, this will open the doors to the application of high-capacity, CNTs-based sorbentsas a better alternative to conventional sorbent in continuous monitoring devices.

  8. Compound list: carbon tetrachloride [Open TG-GATEs

    Lifescience Database Archive (English)

    Full Text Available carbon tetrachloride CCL4 00003 ftp://ftp.biosciencedbc.jp/archive/open-tggates/LATEST/Human/in_vitro/car...ates/LATEST/Rat/in_vitro/carbon_tetrachloride.Rat.in_vitro.Liver.zip ftp://ftp.biosciencedbc.jp/archive/open...-tggates/LATEST/Rat/in_vivo/Liver/Single/carbon_tetrachloride.Rat.in_vivo.Liver.S...ingle.zip ftp://ftp.biosciencedbc.jp/archive/open-tggates/LATEST/Rat/in_vivo/Liver/Repeat/carbon_tetrachloride.Rat.in_vivo.Liver.Repeat.zip ...

  9. Determination of carbon in uranium and its compounds

    International Nuclear Information System (INIS)

    This paper collects the analytical methods used our laboratories for the determination of carbon in uranium metal, uranate salts and the oxides, fluorides and carbides of uranium. The carbon is usually burned off in a induction or resistance oven under oxygen flow. The CO2 is collected in barite solution. Where it is backtitrated with potassium biphthalate. (Author)

  10. Carbon dioxide laser absorption spectra of toxic industrial compounds

    International Nuclear Information System (INIS)

    CO2 laser absorption cross-section data are reported for acrolein, styrene, ethyl acrylate, trichloroethylene, vinyl bromide, and vinylidene chloride. These data indicate that sub parts per billion level, interference-free detection limits should be possible for these compounds by the CO2 laser photoacoustic technique. Photoacoustic detectabilities below 40 ppb should be possible for these compounds in the presence of ambient air concentrations of water vapor and other anticipated interferences. These compounds are also found not to be important inerference in the detection of toxic hydrazine-based rocket fuels by CO2 laser spectroscopic techniques

  11. Differential monitoring of tritium and carbon-14 compounds

    International Nuclear Information System (INIS)

    A gaseous sampling system was developed to differentially collect all major volatile forms of tritium and carbon-14 according to chemical class. These chemical forms include: tritiated forms of water, hydrogen and organics; as well as 14C-containing carbon monoxide, carbon dioxide and organics. Sampling campaigns involving the use of this differential 3H and 14C collection system have been successfully conducted at a high level liquid waste solidification plant, at a spent fuel storage facility and in the vicinity of power reactors

  12. Mechanisms of Microwave Absorption in Carbon Compounds from Shungite

    OpenAIRE

    S. Emelyanov; A. Kuzmenko; V. Rodionov; M. Dobromyslov

    2013-01-01

    According to SEM, X-ray phase analysis, Raman scattering data features of nanostructural changes in shungite carbon structure were found when processing shungite in 52 % hydrofluoric acid. It is found that conductivity increases up to the values of electrical graphite and absorption of microwave radiation also increases at frequencies up to 40 GHz, which, along with dielectric losses, is due to intense processes of both scattering at laminar carbon structures and absorption of electromagnetic...

  13. Mechanisms of Microwave Absorption in Carbon Compounds from Shungite

    Directory of Open Access Journals (Sweden)

    S. Emelyanov

    2013-12-01

    Full Text Available According to SEM, X-ray phase analysis, Raman scattering data features of nanostructural changes in shungite carbon structure were found when processing shungite in 52 % hydrofluoric acid. It is found that conductivity increases up to the values of electrical graphite and absorption of microwave radiation also increases at frequencies up to 40 GHz, which, along with dielectric losses, is due to intense processes of both scattering at laminar carbon structures and absorption of electromagnetic energy.

  14. Carbon Nanomaterials Based Electrochemical Sensors/Biosensors for the Sensitive Detection of Pharmaceutical and Biological Compounds

    OpenAIRE

    Bal-Ram Adhikari; Maduraiveeran Govindhan; Aicheng Chen

    2015-01-01

    Electrochemical sensors and biosensors have attracted considerable attention for the sensitive detection of a variety of biological and pharmaceutical compounds. Since the discovery of carbon-based nanomaterials, including carbon nanotubes, C60 and graphene, they have garnered tremendous interest for their potential in the design of high-performance electrochemical sensor platforms due to their exceptional thermal, mechanical, electronic, and catalytic properties. Carbon nanomaterial-based el...

  15. Synthesis of Carbon Nanotubes and Volatile Organic Compounds Detection

    OpenAIRE

    Sobri S.; Jasni J.; Yasin Faizah M.; Jamal Siti Hasnawati; Janudin Nurjahirah; Mohd Kasim Noor Azilah

    2016-01-01

    In this work, the adsorption effect of volatile organic compounds (chloroacetophenone, acetonitrile and hexane) towards the change of resistance of CNTs pellet as sensor signal was investigated. CNTs used in this research were synthesized using Floating Catalyst – Chemical Vapor Deposition (FC-CVD) method in optimum condition. The synthesized CNTs were characterized using Scanning Electron Microscopy (SEM), Transmission Electron Microscopy (TEM) and Raman Spectroscopy. The variation of resist...

  16. Microtrapping of volatile organic compounds with carbon nanotubes

    OpenAIRE

    Chaudhery Mustansar Hussain; Chutarat Saridara; Somenath Mitra

    2010-01-01

    Micro-sorbent traps referred to as microtraps serve as integrated concentration-injection devices for continuousmonitoring in gas phase streams. The application of carbon nanotubes as unique sorbents for the fabrication of microtrapsfor the nano-scale adsorption/desorption of volatile organic molecules is presented in this paper. The microtrap applicationrequires high adsorption capacity as well as easy desorbability; the latter being critical for injection mode of these integrateddevices. Th...

  17. Synthesis of Carbon Nanotubes and Volatile Organic Compounds Detection

    Directory of Open Access Journals (Sweden)

    Sobri S.

    2016-01-01

    Full Text Available In this work, the adsorption effect of volatile organic compounds (chloroacetophenone, acetonitrile and hexane towards the change of resistance of CNTs pellet as sensor signal was investigated. CNTs used in this research were synthesized using Floating Catalyst – Chemical Vapor Deposition (FC-CVD method in optimum condition. The synthesized CNTs were characterized using Scanning Electron Microscopy (SEM, Transmission Electron Microscopy (TEM and Raman Spectroscopy. The variation of resistance changes towards the tested gases were recorded using a multimeter. CNTs sensor pellet showed good responses towards the tested gases, however, the sensitivity, response time and recovery time of sensor pellet need to be optimized.

  18. Nitrogen Doped Carbon Nanotubes from Organometallic Compounds: A Review

    Directory of Open Access Journals (Sweden)

    Neil J. Coville

    2010-03-01

    Full Text Available Nitrogen doped carbon nanotubes (N-CNTs have become a topic of increased importance in the study of carbonaceous materials. This arises from the physical and chemical properties that are created when N is embedded in a CNT. These properties include modified chemical reactivity and modified conductivity and mechanical properties. A range of methodologies have been devised to synthesize N-CNTs. One of the procedures uses a floating catalyst in which an organometallic complex is decomposed in the gas phase in the presence of a nitrogen containing reactant to give N-CNTs. Most studies have been limited to ferrocene, ring substituted ferrocene and Fe(CO5. This review covers the synthesis (and properties of N-CNTs and other shaped carbon nanomaterials (SCNMs produced using organometallic complexes. It summarizes the effects that physical parameters such as temperature, pressure, gas flow rates, type and concentration of N source etc. have on the N-CNT type, size and yields as well as the nitrogen content incorporated into the tubes that are produced from organometallic complexes. Proposed growth models for N-CNT synthesis are also reported.

  19. Tracing organic compounds in aerobically altered methane-derived carbonate pipes (Gulf of Cadiz, SW Iberia)

    Science.gov (United States)

    Merinero, Raúl; Ruiz-Bermejo, Marta; Menor-Salván, César; Lunar, Rosario; Martínez-Frías, Jesús

    2012-07-01

    The primary geochemical process at methane seeps is anaerobic oxidation of methane (AOM), performed by methanotrophic archaea and sulfate-reducing bacteria (SRB). The molecular fingerprints (biomarkers) of these chemosynthetic microorganisms can be preserved in carbonates formed through AOM. However, thermal maturity and aerobic degradation can change the original preserved compounds, making it difficult to establish the relation between AOM and carbonate precipitation. Here we report a study of amino acid and lipid abundances in carbonate matrices of aerobically altered pipes recovered from the seafloor of the Gulf of Cadiz (SW Iberian Peninsula). This area is characterized by a complex tectonic regime that supports numerous cold seeps. Studies so far have not determined whether the precipitation of carbonate pipes in the Gulf of Cadiz is a purely chemical process or whether microbial communities are involved. Samples from this site show signs of exposure to oxygenated waters and of aerobic alteration, such as oxidation of authigenic iron sulfides. In addition, the degradation index, calculated from the relative abundance of preserved amino acids, indicates aerobic degradation of organic matter. Although crocetane was the only lipid identified from methanotrophic archaea, the organic compounds detected (n-alkanes, regular isoprenoids and alcohols) are compatible with an origin from AOM coupled with bacterial sulfate reduction (BSR) and subsequent aerobic degradation. We establish a relation among AOM, BSR and pipe formation in the Gulf of Cadiz through three types of analysis: (1) stable carbon and oxygen isotopic composition of carbonate minerals; (2) carbonate microfabrics; and (3) mineralogical composition. Our results suggest that carbonate pipes may form through a process similar to the precipitation of vast amounts of carbonate pavements often found at cold seeps. Our approach suggests that some organic compound patterns, in combination with additional

  20. Concentration-dependent polyparameter linear free energy relationships to predict organic compound sorption on carbon nanotubes

    OpenAIRE

    Zhao, Qing; YANG Kun; Li, Wei; Xing, Baoshan

    2014-01-01

    Adsorption of organic compounds on carbon nanotubes (CNTs), governed by interactions between molecules and CNTs surfaces, is critical for their fate, transport, bioavailability and toxicity in the environment. Here, we report a promising concentration-dependent polyparameter linear free energy relationships (pp-LFERs) model to describe the compound-CNTs interactions and to predict sorption behavior of chemicals on CNTs in a wide range of concentrations (over five orders of magnitude). The dev...

  1. Covering vertically aligned carbon nanotubes with a multiferroic compound

    KAUST Repository

    Mahajan, Amit

    2014-10-30

    This work highlights the possible use of vertically-aligned multiwall carbon nanotubes (VA-MWCNTs) as bottom electrodes for microelectronics, for example for memory applications. As a proof of concept BiFeO3 (BFO) films were fabricated in-situ deposited on the surface of VA-MWCNTs by RF (radio frequency) magnetron sputtering. For in situ deposition temperature of 400 °C and deposition time up to 2 h, BFO films cover the MWCNTs and no damage occurs either in the film or MWCNTs. In spite of the macroscopic lossy polarization behaviour, the ferroelectric nature, domain structure and switching of these conformal BFO films was verified by piezo force microscopy. G type antiferromagnetic ordering with weak ferromagnetic ordering loop was proved for BFO films on VA-MWCNTs having a coercive field of 700 Oe.

  2. Synthesis of Heteroaromatic Compounds by Oxidative Aromatization Using an Activated Carbon/Molecular Oxygen System

    Directory of Open Access Journals (Sweden)

    Masahiko Hayashi

    2009-08-01

    Full Text Available A variety of heteroaromatic compounds, such as substituted pyridines, pyrazoles, indoles, 2-substituted imidazoles, 2-substituted imidazoles, 2-arylbenzazoles and pyrimidin-2(1H-ones are synthesized by oxidative aromatization using the activated carbon and molecular oxygen system. Mechanistic study focused on the role of activated carbon in the synthesis of 2-arylbenzazoles is also discussed. In the final section, we will disclose the efficient synthesis of substituted 9,10-anthracenes via oxidative aromatization.

  3. Improvement of Water-Repellency Homogeneity by Compound Fluorine-Carbon Sprayed Coating and Silane Treatment

    OpenAIRE

    FUTAMATA, Masami; Gai, Xiaohui; ITOH, Hidenobu; 伊藤, 英信

    2004-01-01

    To improve the water-repellency of materials, a composite coating of fluorine-carbon has been developed in this study. A thermal sprayed coating produced by using a compound fluorine-carbon cored wire exhibits excellent water-repellency. However, the contact angles of water of the coating surface show remarkable scatters since the fluorine is usually difficult to be distributed uniformly on the coating surface. To improve the homogeneity of the water-repellency of the thermal sprayed coating,...

  4. Carbon Nanomaterials Based Electrochemical Sensors/Biosensors for the Sensitive Detection of Pharmaceutical and Biological Compounds.

    Science.gov (United States)

    Adhikari, Bal-Ram; Govindhan, Maduraiveeran; Chen, Aicheng

    2015-01-01

    Electrochemical sensors and biosensors have attracted considerable attention for the sensitive detection of a variety of biological and pharmaceutical compounds. Since the discovery of carbon-based nanomaterials, including carbon nanotubes, C60 and graphene, they have garnered tremendous interest for their potential in the design of high-performance electrochemical sensor platforms due to their exceptional thermal, mechanical, electronic, and catalytic properties. Carbon nanomaterial-based electrochemical sensors have been employed for the detection of various analytes with rapid electron transfer kinetics. This feature article focuses on the recent design and use of carbon nanomaterials, primarily single-walled carbon nanotubes (SWCNTs), reduced graphene oxide (rGO), SWCNTs-rGO, Au nanoparticle-rGO nanocomposites, and buckypaper as sensing materials for the electrochemical detection of some representative biological and pharmaceutical compounds such as methylglyoxal, acetaminophen, valacyclovir, β-nicotinamide adenine dinucleotide hydrate (NADH), and glucose. Furthermore, the electrochemical performance of SWCNTs, rGO, and SWCNT-rGO for the detection of acetaminophen and valacyclovir was comparatively studied, revealing that SWCNT-rGO nanocomposites possess excellent electrocatalytic activity in comparison to individual SWCNT and rGO platforms. The sensitive, reliable and rapid analysis of critical disease biomarkers and globally emerging pharmaceutical compounds at carbon nanomaterials based electrochemical sensor platforms may enable an extensive range of applications in preemptive medical diagnostics. PMID:26404304

  5. Carbon Nanomaterials Based Electrochemical Sensors/Biosensors for the Sensitive Detection of Pharmaceutical and Biological Compounds

    Directory of Open Access Journals (Sweden)

    Bal-Ram Adhikari

    2015-09-01

    Full Text Available Electrochemical sensors and biosensors have attracted considerable attention for the sensitive detection of a variety of biological and pharmaceutical compounds. Since the discovery of carbon-based nanomaterials, including carbon nanotubes, C60 and graphene, they have garnered tremendous interest for their potential in the design of high-performance electrochemical sensor platforms due to their exceptional thermal, mechanical, electronic, and catalytic properties. Carbon nanomaterial-based electrochemical sensors have been employed for the detection of various analytes with rapid electron transfer kinetics. This feature article focuses on the recent design and use of carbon nanomaterials, primarily single-walled carbon nanotubes (SWCNTs, reduced graphene oxide (rGO, SWCNTs-rGO, Au nanoparticle-rGO nanocomposites, and buckypaper as sensing materials for the electrochemical detection of some representative biological and pharmaceutical compounds such as methylglyoxal, acetaminophen, valacyclovir, β-nicotinamide adenine dinucleotide hydrate (NADH, and glucose. Furthermore, the electrochemical performance of SWCNTs, rGO, and SWCNT-rGO for the detection of acetaminophen and valacyclovir was comparatively studied, revealing that SWCNT-rGO nanocomposites possess excellent electrocatalytic activity in comparison to individual SWCNT and rGO platforms. The sensitive, reliable and rapid analysis of critical disease biomarkers and globally emerging pharmaceutical compounds at carbon nanomaterials based electrochemical sensor platforms may enable an extensive range of applications in preemptive medical diagnostics.

  6. Characterization of carbon, sulfur and volatile compounds in nuclear fuel U3SI2-AL

    International Nuclear Information System (INIS)

    The scope of this work is to describe the characterization of Carbon, Sulfur and Volatile Compounds in nuclear fuel U3Si2-Al used in a research pool type reactor with 5 KW power capacities, located in Sao Paulo, Brazil. This reactor produces a large range of radioisotopes for radiopharmaceutical needed in Brazil nuclear medicine. The fabrication of the fuel U3Si2-Al plate is the key of the whole assembly production and its quality directly affects the safety and reliability of the fuel assembly performance. For this reason, it is very necessary to analyze the Carbon, Sulfur and Volatile Compounds to avoid damage in the fuel plate. The Carbon and Sulfur are characterized by the method of radio frequency furnace gas extraction system coupled with infrared cell detector. The Volatile Compounds are characterized by the method of heat gas extraction coupled with gravimetric technique. These methods are recommended by American Society for Testing Materials ASTM for nuclear materials. The average carbon and sulfur analyzed are 30 μg/g and 3 μg/g, respectively. The average for Volatile Compounds is 40 μg/g. These results represent satisfactory performance of the fuel inside the nuclear reactor. A statistical laboratory program has been set to validate the data generated in the nuclear fuel material to specify any agreement with the recommended ASTM methods. (author)

  7. Selective adsorption for removal of nitrogen compounds from hydrocarbon streams over carbon-based adsorbents

    Science.gov (United States)

    Almarri, Masoud S.

    The ultimate goal of this thesis is to develop a fundamental understanding of the role of surface oxygen functional groups on carbon-based adsorbents in the adsorption of nitrogen compounds that are known to be present in liquid fuels. N2 adsorption was used to characterize pore structures. The surface chemical properties of the adsorbents were characterized by X-ray photoelectron spectroscopy (XPS) and temperature-programmed desorption (TPD) techniques with a mass spectrometer to identify and quantify the type and concentration of oxygen functional groups on the basis of CO2 and CO evolution profiles. It was found that although surface area and pore size distribution are important for the adsorption process, they are not primary factors in the adsorption of nitrogen compounds. On the other hand, both the type and concentration of surface oxygen-containing functional groups play an important role in determining adsorptive denitrogenation performance. Higher concentrations of the oxygen functional groups on the adsorbents resulted in a higher adsorption capacity for the nitrogen compounds. A fundamental insight was gained into the contributions of different oxygen functional groups by analyzing the changes in the monolayer maximum adsorption capacity, qm, and the adsorption constant, K, for nitrogen compounds on different activated carbons. Acidic functional groups such as carboxylic acids and carboxylic anhydrides appear to contribute more to the adsorption of quinoline, while the basic oxygen functional groups such as carbonyls and quinones enhance the adsorption of indole. Despite the high number of publications on the adsorptive desulfurization of liquid hydrocarbon fuels, these studies did not consider the presence of coexisting nitrogen compounds. It is well-known that, to achieve ultraclean diesel fuel, sulfur must be reduced to a very low level, where the concentrations of nitrogen and sulfur compounds are comparable. The adsorptive denitrogenation and

  8. Synthesis of carbon nanotubes by catalytic pyrolysis method with Feitknecht compound as precursor of NiZnAl catalyst

    Institute of Scientific and Technical Information of China (English)

    Yan Xiaoqi; Liu Quanrun; Zhang Songlin; Zhang Kun; Chen Jiuling; Li Yongdan

    2004-01-01

    Carbon nanotubes are synthesized by catalytic pyrolysis method with a kind of new type catalyst--nickel-zinc-alumina catalyst prepared from Feitknecht compound. Tubular carbon nanotubes, bamboo-shaped carbon naotubes, herringbone carbon nanotubues and branched carbon nanotubes are all found formed at moderate temperature. It is important for the formation of quasi-liquid state of the metal nanoparticles at the tip of carbon naotubes during the growth of carbon nanotubes to lead to different kinds of carbon nanotubes. It is likely that the addition of zinc make the activity of nickel catalyst after calcinations and reduction changed strangely.

  9. Carbon transfer in soil - plant system. Molecular labelling utilization for determining rhizosphere compounds

    International Nuclear Information System (INIS)

    The growing up of the bacteria developing in the rhizosphere of plants is dependent on the compounds exudation by plant roots. Even the bacterial genetics use has permitted to identify diverse functions involved in the process of the rhizosphere colonisation ( mobility, heterotrophic bacteria, growing rate, antibiotics production), there is a big delay in vegetal partners. To decrease this delay we tried to characterize the interactions between a plant model, Arabidopsis thaliana and the rhizosphere bacteria. An experimental device has been conceived for measuring the transfer of carbon issued from the photosynthesis to roots and soil. The exudation by roots has been studied. The analysis of rhizospheric compounds in situ pose some methodological problems, especially, the rhizospheric compounds must be extracted from the soil matrix. we suggest an analysis method of rhizospheric compound and of their dynamics. (F.M.)

  10. Adsorption studies of recalcitrant compounds of molasses spentwash on activated carbons.

    Science.gov (United States)

    Figaro, S; Louisy-Louis, S; Lambert, J; Ehrhardt, J-J; Ouensanga, A; Gaspard, S

    2006-10-01

    Due to high levels of residual chemical oxygen demand (COD) in the effluent of molasses spentwash (MSW) after anaerobic treatment, acceptable COD levels for discharge cannot be achieved without some form of post-treatment. In this study, the particulate composition of molasses spentwash after anaerobic digestion (MSWD), is characterised as to its particle size distribution, using micro- and ultrafiltration and three activated carbons are characterised as to their ability to reduce significantly the COD of MSWD effluent. The activated carbons tested as adsorbent, were characterised by XPS spectroscopy, elemental analysis, surface area, pore size distribution, and acid-base titration using the Boehm's method. Adsorption of phenol, used here as a reference compound, and of some organic compounds contained in MSWD (gallic acid, tannic acid, and melanoidin, respectively), was studied. It was clearly demonstrated that an activated carbon with a significant distribution of both micropores and mesopores and a significant amount of macropores that are assumed to act as conduits providing access to micro- and mesopores, have a good adsorption efficiency for compounds such as tannic acid and melanoidins. It is a good adsorbent for melanoidin and coloured compounds of MSWD, which represents a large source of the aqueous pollution in sugar cane industries. PMID:16987542

  11. Hydrogen isotopic compositions of organic compounds in plants reflect the plant's carbon metabolism

    Science.gov (United States)

    Cormier, M. A.; Kahmen, A.; Werner, R. A.

    2015-12-01

    The main factors controlling δ2H of plant organic compounds are generally assumed to be the plant's source water and the evaporative deuterium enrichment of leaf water. Hydrogen isotope analyses of plant compounds from sediments or tree rings are therefore mainly applied to assess hydrological conditions at different spatial and temporal scales. However, the biochemical hydrogen isotope fractionation occurring during biosynthesis of plant organic compounds (ɛbio) also accounts for a large part of the variability observed in the δ2H values. Nevertheless, only few studies have directly addressed the physiological basis of this variability and even fewer studies have thus explored possible applications of hydrogen isotope variability in plant organic compounds for plant physiological research. Here we show two datasets indicating that the plant's carbon metabolism can have a substantial influence on δ2H values of n-alkanes and cellulose. First, we performed a controlled experiment where we forced plants into heterotrophic and autotrophic C-metabolism by growing them under four different light treatments. Second, we assessed the δ2H values of different parasitic heterotrophic plants and their autotrophic host plants. Our two datasets show a systematic shift in ɛbio of up to 80 ‰ depending on the plant's carbon metabolism (heterotrophic or autotrophic). Differences in n-alkane and cellulose δ2H values in plants with autotrophic vs. heterotrophic metabolisms can be explained by different NADPH pools that are used by the plants to build their compounds either with assimilates that originate directly from photosynthesis or from stored carbohydrates. Our results have significant implications for the calibration and interpretation of geological records. More importantly, as the δ2H values reflect the plant's carbon metabolism involved during the tissue formation, our findings highlight the potential of δ2H values as new tool for studying plant and ecosystem carbon

  12. Carbon isotope analysis of carbonaceous compounds in Puget Sound and Lake Washington

    International Nuclear Information System (INIS)

    A new method has been developed and tested for determining chronological profiles of organic pollutants. This method, Carbon Isotope Analysis (CIA), involves measurements of 12C, 13C and 14C in carbonaceous compounds found in layers of sediment. Lipids, total aliphatic hydrocarbons (TAHs) and polycyclic aromatic hydrocarbons (PAHs) are separated from kg quantities of sediment. Large Soxhlet extractors are used to remove the extractable organics, using ultra-pure benzene-methanol solution and having an extraction efficiency of about 86% for compounds with boiling points higher than n-tetradecane (n-C14). The basic steps in compound separation include freeze-drying, extraction, fractionation, column chromatography and evaporation. Isolating the TAH and PAH fractions is accomplished by eluting samples from Sephadex and alumina/silica-gel columns. The amount of each fraction recovered is determined by converting the hydrocarbons to carbon dioxide and measuring this gas manometrically. Variations in 12C and 13C abundances for carbonaceous compounds are primarily due to thermodynamic, photosynthetic and metabolic fractionation processes. Thus, the source of a particular organic compound can often be determined by measuring its 13C/12C ratio. Combining the information from both the 13C analysis and 14C analysis makes source identification more certain. In addition, this investigation reviews carbon isotopic data and carbon cycling and analyzes organic pollution in two limited ecosystems (Puget Sound and Lake Washington). Specifically, distinct carbonaceous species are analyzed for pollution in sediments of Lake Washington, Elliott Bay, Commencement Bay, central Puget Sound and northern Puget Sound near the Cherry Point oil refineries

  13. Correlation and prediction of adsorption capacity and affinity of aromatic compounds on carbon nanotubes.

    Science.gov (United States)

    Wu, Wenhao; Yang, Kun; Chen, Wei; Wang, Wendi; Zhang, Jie; Lin, Daohui; Xing, Baoshan

    2016-01-01

    Adsorption of 22 nonpolar and polar aromatic compounds on 10 carbon nanotubes (CNTs) with various diameters, lengths and surface oxygen-containing group contents was investigated to develop predictive correlations for adsorption, using the isotherm fitting of Polanyi theory-based Dubinin-Ashtakhov (DA) model. Adsorption capacity of aromatic compounds on CNTs is negatively correlated with melting points of aromatic compounds, and surface oxygen-containing group contents and surface area ratios of mesopores to total pores of CNTs, but positively correlated with total surface area of CNTs. Adsorption affinity is positively correlated with solvatochromic parameters of aromatic compounds, independent of tube lengths and surface oxygen-containing group contents of CNTs, but negatively correlated with surface area ratios of mesopores to total pores of CNTs. The correlations of adsorption capacity and adsorption affinity with properties of both aromatic compounds and CNTs clearly have physical significance, can be used successfully with DA model to predict adsorption of aromatic compounds on CNTs from the well-known physiochemical properties of aromatic compounds (i.e., solvatochromic parameters, melting points) and CNTs (i.e., surface area and total acidic group contents), and thus can facilitate the environmental application of CNTs as sorbents and environmental risk assessment of both aromatic contaminants and CNTs. PMID:26521219

  14. Possibility of diacetyl and related compounds as the 4-carbon compound necessary for the formation of riboflavin in Ashbya gossypii.

    Science.gov (United States)

    Nakajima, K; Mitsuda, H

    1984-01-01

    The effects of various compounds (0.5%) involved in the butanediol and the glycolytic pathways on riboflavin formation in whole cells of Ashbya gossypii at rest were examined. The addition of acetate, glycerol and diacetyl inhibited riboflavin formation, while the addition of acetoin had no effect on it, and the addition of ethanol, 2,3-butanediol, pyruvic acid and glucose accelerated it. The relation of diacetyl and acetoin to riboflavin formation during resting cell incubation in the presence of 0.5% ethanol and various concentrations of 2,3-butanediol was examined. The results quantitatively revealed a precursor-product relation between riboflavin formation and the formation of diacetyl and acetoin. The results obtained provide evidence that a high flavinogenic agent, ethanol, was converted to acetaldehyde, pyruvic acid, acetoin and diacetyl in this order, that a week flavinogenic agent, 2,3-butanediol, was transferred to diacetyl through acetoin, and that the diacetyl produced can be utilized as the 4-carbon compound for riboflavin formation in the flavinogenic mold, Ashbya gossypii. It remains obscure whether diacetyl is enzymatically involved in riboflavin formation. PMID:6534171

  15. Catalytic Conversion of Carbon-Containing Compounds into Valuable Chemicals and Fuels

    Science.gov (United States)

    Cheng, Zhuo

    Conversion of carbon-containing compounds, especially C1 compounds such as carbon dioxide and methane, to valuable chemicals and fuels will hopefully address concerns over decreasing supplies of fossil fuels and mitigate the eects of greenhouse gas emissions on global climate change. Many challenges, however, remain to be addressed before these technologies may be adopted on an industrial scale. Chiefly, catalysts must be developed to activate carbon-containing compounds from their thermodynamically stable ground states, using hydrogen, electrons, or heat as energy sources. We chose as model catalytic systems: 1) Metathesis of ethene and 2-butene; 2) Methane dehydrogenation and carbon dioxide hydrogenation. We developed three computational methodologies to study these processes across a range of length and time scales. First, we investigated how electronic structure affects the properties and reactivity of these catalyst systems; by computing the partial electronic density of states, electronic localization function, and excess spin density, we showed how redox supports, such as ceria, promote electron transfer reactions. We applied this to the studies of methane activation and carbon dioxide activation. Second, we developed a non-equilibrium thermodynamics approach to calculate energies of activation at nite temperatures, based on the Bronsted-Evans-Polanyi principle and the Nudged Elastic Band method. Third, we developed an approach to numerically compute heat capacities and other thermodynamic properties on extended catalytic systems that are comparable in accuracy and precision to methods that have been well-developed for gas-phase molecules. We applied these to the studies of metathesis propagation and carbon dioxide hydrogenation. We gained mechanistic, thermodynamic, and kinetic insight into the elementary steps that comprise larger reaction networks of interest to the broader catalysis community. Ultimately, these theoretical and computational predictions

  16. Electrically Conductive Compounds of Polycarbonate, Liquid Crystalline Polymer, and Multiwalled Carbon Nanotubes

    OpenAIRE

    Penwisa Pisitsak; Rathanawan Magaraphan; Sadhan C. Jana

    2012-01-01

    A thermotropic liquid crystalline polymer (LCP) was blended with polycarbonate (PC) and multiwalled carbon nanotube (CNT) with the goal of improving electrical conductivity and mechanical properties over PC. The LCP was anticipated to produce fibrillar domains in PC and help improve the mechanical properties. The study was carried out using two grades of LCP—Vectra A950 (VA950) and Vectra V400P (V400P). The compounds contained 20 wt% LCP and 0.5 to 15 wt% CNT. The compounds were prepared by m...

  17. Organic carbon transformation in agricultural soils : radiocarbon analysis of organic matter fractions and biomarker compounds

    OpenAIRE

    Rethemeyer, Janet

    2004-01-01

    Radiocarbon analyses of physical and chemical soil organic matter fractions as well as of individual compounds provided information on the origin, transformation and stabilisation of organic carbon in agricultural soils. A contamination of the soil at the study site at Halle/Saale (Germany) with fossil, lignite-derived carbon was identified by high apparent 14C ages of the organic matter in the plough horizon of about 5000 years BP and a decrease in 14C age with increasing soil depth. The fos...

  18. Carbon compound used in hydrogen storage; Compuesto de carbon utilizado en almacenamiento de hidrogeno

    Energy Technology Data Exchange (ETDEWEB)

    Iturbe G, J.L.; Lopez M, B.E. [ININ, 52045 Ocoyoacac, Estado de Mexico (Mexico)

    2004-07-01

    In the present work it is studied the activated carbon of mineral origin for the sorption of hydrogen. The carbon decreased of particle size by means of the one alloyed mechanical. The time of mill was of 10 hours. The characterization one carries out by scanning electron microscopy and X-ray diffraction. The hydrogen sipped in the carbon material it was determined using the Thermal gravimetric method (TGA). The conditions of hydrogenation went at 10 atm of pressure and ambient temperature during 18 hours. They were also carried out absorption/desorption cycles of hydrogen in the same one system of thermal gravimetric analysis. The results showed percentages of sorption of 2% approximately in the cycles carried out in the system TGA and of 4.5% in weight of hydrogen at pressure of 10 atmospheres and ambient temperature during 18 hours. (Author)

  19. Carbon functionalized mesoporous silica-based gas sensors for indoor volatile organic compounds.

    Science.gov (United States)

    Liu, Yupu; Chen, Junchen; Li, Wei; Shen, Dengke; Zhao, Yujuan; Pal, Manas; Yu, Haijun; Tu, Bo; Zhao, Dongyuan

    2016-09-01

    Indoor organic gaseous pollution is a global health problem, which seriously threats the health and life of human all over the world. Hence, it is important to fabricate new sensing materials with high sensitivity and efficiency for indoor volatile organic compounds. In this study, a series of ordered mesoporous silica-based nanocomposites with uniform carbon coatings on the internal surface of silica mesopore channels were synthesized through a simple template-carbonization strategy. The obtained mesoporous silica-carbon nanocomposites not only possess ordered mesostructures, high surface areas (up to ∼759m(2)g(-1)), large and tunable pore sizes (2.6-10.2nm), but also have the improved hydrophobicity and anti-interference capability to environmental humidity. The sensing performances of the mesoporous silica-carbon nanocomposites to volatile organic compounds, such as ethylbenzene, methylbenzene, benzene, methanol, acetone, formaldehyde, dichloromethane and tetrahydrofuran, were systematically investigated. The relationships between the sensing performances and their properties, including mesostructures, surface areas, pore sizes, carbon contents and surface hydrophilic/hydrophobic interactions, have been achieved. The mesoporous silica-carbon nanocomposites with hexagonal mesostructure exhibit outstanding performance at room temperature to benzene and acetone with high responses, short response (2-3s) and recovery (16-19s) time, strong anti-interference to environmental humidity, and long-term stability (less than ∼5% loss of the frequency shifts after 42days). Therefore, the obtained mesoporous silica-carbon nanocomposites have a hopeful prospect in the field of environmental air quality monitoring. PMID:27240244

  20. O-methylation of natural phenolic compounds based on green chemistry using dimethyl carbonate

    Science.gov (United States)

    Prakoso, N. I.; Pangestu, P. H.; Wahyuningsih, T. D.

    2016-02-01

    The alkyl aryl ether compounds, of which methyl eugenol and veratraldehyde are the simplest intermediates can be synthesized by reacting eugenol and vanillin with the green reagent dimethyl carbonate (DMC). The reaction was carried out under mild of temperature and pressure. Excellent yields and selective products were obtained (95-96%) after a few hours. In the end of the reaction, the catalysts (base and Phase Transfer Catalyst) can be recovered and regenerated.

  1. Angle-Dependent Electron Spectroscopy Studies of C60 Compounds and Carbon Nanotubes

    OpenAIRE

    Schiessling, Joachim

    2003-01-01

    Fullerenes have been shown to constitute a prototypical building block for truly nanometer-sized devices and exotic nanounit-based materials, e.g., high-temperature superconductors. This makes the detailed understanding of fullerene electronic states in compounds and at interfaces of primary importance, since the high symmetry of the molecule greatly simplifies the starting point of the analysis. Carbon nanotubes, which combine one macroscopic with two nanoscopic dimensions, are perhaps of e...

  2. Supercritical Carbon Dioxide Extraction of Bioactive Compounds from Ampelopsis grossedentata Stems: Process Optimization and Antioxidant Activity

    OpenAIRE

    Da Sun; Shikang Zhang; Yuefei Wang; Ping Xu; Yuejin Zhu; Le Ying

    2011-01-01

    Supercritical carbon dioxide (SC-CO2) extraction of bioactive compounds including flavonoids and phenolics from Ampelopsis grossedentata stems was carried out. Extraction parameters such as pressure, temperature, dynamic time and modifier, were optimized using an orthogonal array design of L9 (34), and antioxidant activities of the extracts were evaluated by 2,2-diphenyl-1-picrylhydrazyl (DPPH) free radical scavenging assay and ferrous ion chelating (FIC) assay. The best conditions obtained f...

  3. Impact of the addition of a compound fertilizer on the dissolution of carbonate rock tablets: A column experiment

    International Nuclear Information System (INIS)

    Highlights: → Impact of compound fertilizer on carbonate dissolution is studied by columns. → Compound fertilizer reduced soil pH and increased the leach of ions. → Carbonate dissolution accelerated due to compound fertilizer application. → Impact of fertilizer on the budget of CO2 sink cannot be disregarded. - Abstract: The chemical weathering dynamics of carbonate and the C cycle are strongly influenced by anthropogenic perturbations such as agricultural fertilization. In this study, two columns (a control column and a fertilizer column) with carbonate rock tablets in the bottom of each were established to explore the impact of the addition of a compound fertilizer on the dissolution of carbonate rock tablets. The impacts were assessed from hydro-chemical analyses of the leachates from the two columns and comparison of the amount of dissolution of the carbonate rock tablets. The results showed that NH4+, free CO2, HCO3-,HPO42- and COD increased in the leachate after addition of the compound fertilizer, whereas the pH decreased. The pH decrease was attributed to the release of protons from the nitrification reaction. The amount of dissolution of limestone and dolomite tablets decreased as a result of the compound fertilizer application. Furthermore, the calculated results using Phreeqci software showed that the compound fertilizer reduced the saturation index of calcite and dolomite. Thus, the impact of a compound fertilizer, especially an ammonium fertilizer, on the budget of the CO2 sink cannot be disregarded on either a regional or a global scale.

  4. Immobilization of Bacillus sp. in mesoporous activated carbon for degradation of sulphonated phenolic compound in wastewater

    International Nuclear Information System (INIS)

    Xenobiotic compounds are used in considerable quantities in leather industries besides natural organic and inorganic compounds. These compounds resist biological degradation and thus they remain in the treated wastewater in the unaltered molecular configurations. Immobilization of organisms in carrier matrices protects them from shock load application and from the toxicity of chemicals in bulk liquid phase. Mesoporous activated carbon (MAC) has been considered in the present study as the carrier matrix for the immobilization of Bacillus sp. isolated from Effluent Treatment Plant (ETP) employed for the treatment of wastewater containing sulphonated phenolic (SP) compounds. Temperature, pH, concentration, particle size and mass of MAC were observed to influence the immobilization behavior of Bacillus sp. The percentage immobilization of Bacillus sp. was the maximum at pH 7.0, temperature 20 °C and at particle size 300 μm. Enthalpy, free energy and entropy of immobilization were − 46.9 kJ mol−1, − 1.19 kJ mol−1 and − 161.36 J K−1 mol−1 respectively at pH 7.0, temperature 20 °C and particle size 300 μm. Higher values of ΔH0 indicate the firm bonding of the Bacillus sp. in MAC. Degradation of aqueous sulphonated phenolic compound by Bacillus sp. immobilized in MAC followed pseudo first order rate kinetics with rate constant 1.12 × 10−2 min−1. Highlights: ► Degradation on phenolic syntan using immobilized activated carbon as catalyst. ► Bacillus sp. immobilized cell reactor removed all refractory organic loads. ► The removal mechanism is due to co-metabolism between carbon and organisms. ► The organics are completely metabolized rather than adsorption.

  5. Immobilization of Bacillus sp. in mesoporous activated carbon for degradation of sulphonated phenolic compound in wastewater

    Energy Technology Data Exchange (ETDEWEB)

    Sekaran, G., E-mail: ganesansekaran@gmail.com [Environmental Technology Division, Council of Scientific and Industrial Research (CSIR), Central Leather Research Institute (CLRI), Adyar, Chennai-600 020 (India); Karthikeyan, S. [Environmental Technology Division, Council of Scientific and Industrial Research (CSIR), Central Leather Research Institute (CLRI), Adyar, Chennai-600 020 (India); Gupta, V.K. [Department of Chemistry, Indian Institute of Technology Roorkee, Roorkee-247 667 (India); Department of Chemistry, King Fahd University of Petroleum and Minerals, Dhahran 31261 (Saudi Arabia); Boopathy, R.; Maharaja, P. [Environmental Technology Division, Council of Scientific and Industrial Research (CSIR), Central Leather Research Institute (CLRI), Adyar, Chennai-600 020 (India)

    2013-03-01

    Xenobiotic compounds are used in considerable quantities in leather industries besides natural organic and inorganic compounds. These compounds resist biological degradation and thus they remain in the treated wastewater in the unaltered molecular configurations. Immobilization of organisms in carrier matrices protects them from shock load application and from the toxicity of chemicals in bulk liquid phase. Mesoporous activated carbon (MAC) has been considered in the present study as the carrier matrix for the immobilization of Bacillus sp. isolated from Effluent Treatment Plant (ETP) employed for the treatment of wastewater containing sulphonated phenolic (SP) compounds. Temperature, pH, concentration, particle size and mass of MAC were observed to influence the immobilization behavior of Bacillus sp. The percentage immobilization of Bacillus sp. was the maximum at pH 7.0, temperature 20 Degree-Sign C and at particle size 300 {mu}m. Enthalpy, free energy and entropy of immobilization were - 46.9 kJ mol{sup -1}, - 1.19 kJ mol{sup -1} and - 161.36 J K{sup -1} mol{sup -1} respectively at pH 7.0, temperature 20 Degree-Sign C and particle size 300 {mu}m. Higher values of {Delta}H{sup 0} indicate the firm bonding of the Bacillus sp. in MAC. Degradation of aqueous sulphonated phenolic compound by Bacillus sp. immobilized in MAC followed pseudo first order rate kinetics with rate constant 1.12 Multiplication-Sign 10{sup -2} min{sup -1}. Highlights: Black-Right-Pointing-Pointer Degradation on phenolic syntan using immobilized activated carbon as catalyst. Black-Right-Pointing-Pointer Bacillus sp. immobilized cell reactor removed all refractory organic loads. Black-Right-Pointing-Pointer The removal mechanism is due to co-metabolism between carbon and organisms. Black-Right-Pointing-Pointer The organics are completely metabolized rather than adsorption.

  6. Adsorption of Thiophenic Compounds from Model Diesel Fuel Using Copper and Nickel Impregnated Activated Carbons

    Directory of Open Access Journals (Sweden)

    Ramin Karimzadeh

    2012-10-01

    Full Text Available Adsorption of sulfur compoundsby porous materials is an effective way to produce cleaner diesel fuel.In this study, adsorption of refractory thiophenic sulfur compounds, i.e., benzothiophene (BT, dibenzothiophene (DBT, and 4,6-dimethyldibenzothiophene (4,6-DMDBT in single-solute systems from n-hexane solutions onto metal-impregnated activated carbons was investigated. A hydrogen-treated activated carbon fiber was selectively loaded with Ni, NiO, Cu, Cu2O, and CuO species to systematically assess the impact of each metal species on the adsorption of thiophenic compounds (TC. Metal-loaded adsorbents had the same total metal contents and similar microporosities, but contained different types of copper or nickel species. All metal-loaded adsorbents showed enhanced adsorption of tested TC. Cu2O- or NiO-loaded adsorbents exhibited the highest uptakes, due to more specific interactions between Cu+ or Ni2+ species and TC molecules. The theoretical monolyer coverage of TC on the exposed Cu+ sites was estimated and compared with that calculated from the experimental data. Results suggested catalytic conversion of TC molecules to other compounds on the Cu+ sites, followed by adsorption of reaction products onto the carbon surface or multilayer accumulation of TC molecules on the Cu+sites. TC adsorption uptake of the majority of adsorbents followed the order of: 4,6-DMDBT > DBT > BT due to higher intensity of specific and non-specific interactions of larger TC molecules with adsorbents.

  7. Visualizing lone pairs in compounds containing heavier congeners of the carbon and nitrogen group elements

    Indian Academy of Sciences (India)

    Ram Seshadri

    2001-10-01

    In this mini-review, I discuss some recent work on the stereochemistry and bonding of lone pairs of electrons in divalent compounds of the heavier carbon group elements (SnII, PbII) and in trivalent compounds of the heavier nitrogen group elements (BiIII). Recently developed methods that permit the real-space visualization of bonding patterns on the basis of density functional calculations of electronic structure, reveal details of the nature of selectron lone pairs in compounds of the heavier main group elements - their stereochemistry and their inertness (or lack thereof). An examination of tetragonal 4/ SnO, -PbO and BiOF, and cubic $\\bar{3}$ PbS provides a segue into perovskite phases of technological significance, including ferroelectric PbTiO3 and antiferroelectric/piezoelectric PbZrO3, in both of which the lone pairs on Pb atoms play a pivotal rôle.

  8. The electrochemical performance of ordered mesoporous carbon/nickel compounds composite material for supercapacitor

    International Nuclear Information System (INIS)

    A series of high performance ordered mesoporous carbon/nickel compounds composites have been synthesized by a combination of incipient wetness impregnation and hydrothermal method for the first time. X-ray diffraction (XRD), N2 adsorption/desorption isotherms and transmission electron microscopy (TEM) are used to characterize the composites derived at the hydrothermal temperature of 125, 150, 175, 200, 250, 275 and 300 oC. The formation of nanosized nickel compounds, fully inside the mesopore system, was confirmed with XRD and TEM. An N2 adsorption/desorption isotherms measurements still revealed mesoporosity for the host/guest compounds. It is noteworthy that an OMC/nickel nitrate hydroxide hydrate composite (OMCN-150) exhibits more excellent performance. Based on the various hydrothermal temperatures of the composite, the capacitance of an OMCN-150 delivering the best electrochemical performance is about 2.4 (5 mV s-1) and 1.5 (50 mV s-1) times of the pristine OMC. The capacitance retention of an OMCN-150 is 96.1%, which indicates that the electrochemical performance of the supercapacitor is improved greatly, and represents novel research and significant advances in the field of electrode composite materials for supercapacitor. -- Graphical abstract: A series of high performance nickel compound/ordered mesoporous carbon composites were synthesized by a combination of incipient wetness impregnation and hydrothermal method for the first time. Display Omitted

  9. Single, competitive, and dynamic adsorption on activated carbon of compounds used as plasticizers and herbicides.

    Science.gov (United States)

    Abdel daiem, Mahmoud M; Rivera-Utrilla, José; Sánchez-Polo, Manuel; Ocampo-Pérez, Raúl

    2015-12-15

    The main aim of this study was to investigate the single, competitive, and dynamic adsorption of phthalic acid (PA), bisphenol A (BPA), diphenolic acid (DPA), 2,4-dichlorophenoxy-acetic acid (2,4-D), and 4-chloro-2-methylphenoxyacetic acid (MCPA) on two activated carbons with different chemical natures and similar textural characteristics. The adsorption mechanism was also elucidated by analyzing the influence of solution pH and ionic strength. The activated carbons demonstrated high adsorption capacity to remove all micropollutants due to the presence of active sites on their surfaces, which increase dispersive interactions between the activated carbon graphene layers and the aromatic ring of pollutants. The adsorption capacity of the activated carbons increased in the order: DPAcarbon decreased by around 50% and 70% in the presence of DPA and BPA, respectively, indicating that both compounds are adsorbed on the same adsorption sites of the activated carbon. PMID:26282767

  10. Steam reforming of cyclic model compounds of bio-oil over Ni-based catalysts: Product distribution and carbon formation

    DEFF Research Database (Denmark)

    Trane-Restrup, Rasmus; Jensen, Anker Degn

    2015-01-01

    significantly by adding oxygen to the feed at a cost of a lower yield of H2. Stable operation was observed initially (first 4h) in the OSR of all compounds, but experiments over 24h showed signs of deactivation due to an accelerated rate of carbon deposition in the SR of furfural and guaiacol. Furthermore...... yields in the SR of guaiacol and temperatures of 780°C were needed to totally convert guaiacol to carbon oxides and H2.Carbon deposition was observed in the SR of all three model compounds and was most severe for guaiacol followed by furfural and 2-methylfuran. The carbon deposition could be reduced...

  11. Sorption of organic carbon compounds to the fine fraction of surface and Subsurface Soils

    Energy Technology Data Exchange (ETDEWEB)

    Jagadamma, Sindhu [ORNL; Mayes, Melanie [ORNL; Zinn, Yuri [Federal University of Lavras, Brazil; Gisladottir, Gudrun [University of Iceland; Ann, Russell [Iowa State University

    2014-01-01

    Dissolved organic carbon (DOC) transported from the soil surface is stabilized in deeper soil profiles by physicochemical sorption processes. However, it is unclear how different forms of organic carbon (OC) compounds common in soil organic matter interact with soil minerals in the surface (A) and subsurface (B) horizons. We added four compounds (glucose, starch, cinnamic acid and stearic acid) to the silt- and clay-sized fraction (fine fraction) of A and B horizons of eight soils from varying climates (3 temperate, 3 tropical, 1 arctic and 1 sub-arctic). Equilibriumbatch experiments were conducted using 0 to 100 mg C L 1 of 14C-labeled compounds for 8 h. Sorption parameters (maximum sorption capacity, Qmax and binding coefficient, k) calculated by fitting sorption data to the Langmuir equation showed that Qmax of A and B horizons was very similar for all compounds. Both Qmax and k values were related to sorbate properties, with Qmax being lowest for glucose (20 500 mg kg 1), highest for stearic acid (20,000 200,000 mg kg 1), and intermediate for both cinnamic acid (200 4000 mg kg 1) and starch (400 6000 mg kg 1). Simple linear regression analysis revealed that physicochemical properties of the sorbents influenced the Qmax of cinnamic acid and stearic acid, but not glucose and starch. The sorbent properties did not show predictive ability for binding coefficient k. By using the fine fraction as sorbent, we found that the mineral fractions of A horizons are equally reactive as the B horizons irrespective of soil organic carbon content.

  12. Emissions of carbon species, organic polar compounds, potassium, and mercury from prescribed burning activities

    Science.gov (United States)

    Zhang, Y.; Obrist, D.; Zielinska, B.; Gerler, A.

    2012-04-01

    Biomass burning is an important emission source of pollutants to the atmosphere, but few studies have focused on the chemical composition of emissions from prescribed burning activities. Here we present results from a sampling campaign to quantify particulate-phase emissions from various types of prescribed fires including carbon species (Elemental Carbon: EC; Organic Carbon: OC; and Total Carbon: TC); polar organic compounds (12 different compounds and four functional classes); water-soluble potassium (K+); and mercury (Hg). We measured emissions from the following types of prescribed biomass burning in the Lake Tahoe basin located on the California/Nevada border: (i) log piles stacked and dried in the field; (ii) log piles along with green understory vegetation; and (iii) understory green vegetation and surface litter; further emissions were collected from burns conducted in a wood stove: (iv) dried wooden logs; (v) green foliage of understory vegetation collected from the field; and (vi) surface organic litter collected from the field; finally, samples were also taken from (vii) ambient air in residential areas during peak domestic wood combustion season. Results show that OC/EC ratios of prescribed burns in the field ranged from 4 to 10, but lower values (around 1) were observed in controlled stove fires. These results are consistent with an excess of OC emissions over EC found in wildfires. OC/EC ratios, however, showed clear separations between controlled wood stove combustion (higher EC) and prescribed burns in the field (lower EC). We attribute this difference to a higher combustion temperatures and dominance of flaming combustion in wood stove fires. OC positively and linearly correlated to the sum of polar organic compounds across all burn types (r2 of 0.82). The most prevalent group of polar compounds emitted during prescribed fires was resin acids (dehydroabietic, pimaric, and abietic acids), followed by levoglucosan plus mannositol. Negligible

  13. The Effects of Silica/Carbon Black Ratio on the Dynamic Properties of the Tread compounds in Truck Tires

    OpenAIRE

    Zafarmehrabian, Ramin; Gangali, Saeed Taghvaei; Ghoreishy, Mir Hamid Reza; Davallu, Mehran

    2012-01-01

    NR is the major constituent in the rubber compound used for the tread on the truck tires. A general compound formulation of the tire tread includes NR and BR as polymer base and carbon black as the reinforcing filler, and curative components. In this paper the effects of dual filler system (carbon black and precipitated silica) on the dynamic properties of tire treat has been studied. The results show by increasing of precipitated silica, significant improvement was observed in fatigue resist...

  14. Linear solvation energy relationships (LSER) for adsorption of organic compounds by carbon nanotubes.

    Science.gov (United States)

    Ersan, Gamze; Apul, Onur G; Karanfil, Tanju

    2016-07-01

    The objective of this paper was to create a comprehensive database for the adsorption of organic compounds by carbon nanotubes (CNTs) and to use the Linear Solvation Energy Relationship (LSER) technique for developing predictive adsorption models of organic compounds (OCs) by multi-walled carbon nanotubes (MWCNTs) and single-walled carbon nanotubes (SWCNTs). Adsorption data for 123 OCs by MWCNTs and 48 OCs by SWCNTs were compiled from the literature, including some experimental results obtained in our laboratory. The roles of selected OCs properties and CNT types were examined with LSER models. The results showed that the r(2) values of the LSER models displayed small variability for aromatic compounds smaller than 220 g/mol, after which a decreasing trend was observed. The data available for aliphatics was mainly for molecular weights smaller than 250 g/mol, which showed a similar trend to that of aromatics. The r(2) values for the LSER model on the adsorption of aromatic and aliphatic OCs by SWCNTs and MWCNTs were relatively similar indicating the linearity of LSER models did not depend on the CNT types. Among all LSER model descriptors, V term (molecular volume) for aromatic OCs and B term (basicity) for aliphatic OCs were the most predominant descriptors on both type of CNTs. The presence of R term (excess molar refractivity) in LSER model equations resulted in decreases for both V and P (polarizability) parameters without affecting the r(2) values. Overall, the results demonstrate that successful predictive models can be developed for the adsorption of OCs by MWCNTs and SWCNTs with LSER techniques. PMID:27064209

  15. Exposure to carbon monoxide, respirable suspended particulates, and volatile organic compounds while commuting by bicycle

    International Nuclear Information System (INIS)

    A portable air sampling system has been used to assess exposures to various substances while commuting by bicycle in an urban area. The major source of pollutants in this situation is motor vehicle exhaust emissions. Carbon monoxide, measured by electrochemical detection, was found at peak concentrations in excess of 62 ppm, with mean values over 16 individual 35-mm journeys being 10.5 ppm. Respirable suspended particulates, averaged over each journey period, were found at higher concentrations (mean 130 μg m-3) than would be expected in indoor situations. Mean exposure to benzene (at 56 μg m-3) and other aromatic volatile organic compounds was also relatively high. The influence of wind conditions on exposure was found to be significant. Commuting exposures to carbon monoxide, respirable suspended particulates, and aromatic VOCs were found to be higher than exposures in a busy high street and on common parkland

  16. General synthesis of carbon nanocages and their adsorption of toxic compounds from cigarette smoke

    Science.gov (United States)

    Li, Guangda; Yu, Hongxiao; Xu, Liqiang; Ma, Qiang; Chen, Chao; Hao, Qin; Qian, Yitai

    2011-08-01

    Carbon nanocages (CNCs) have been synthesized through a simple approach using different alcohols and ferrous oxalate as reactants at 550 °C for 12 h in a sealed autoclave. The lengths of the sides of the CNCs are about 200-350 nm and the wall thicknesses are about 10-15 nm. The formation mechanism of the CNCs is also discussed, based on the experimental results. These CNCs show excellent removal efficiency for phenolic compounds, ammonia, and total particulate matter from cigarette smoke. The adsorption capability of CNCs prepared from ethanol is much higher than that of other samples. For example, the efficiency of 5 mg CNCs (ethanol) for removing the six phenolic compounds p-dihydroxybenzene, m-dihydroxybenzene, o-dihydroxybenzene, phenol, m-cresol, and o-cresol can reach 57.31%, 62.25%, 65.58%, 75.95%, 54.34% and 59.43%, respectively, while that of the commercial activated carbon (5 mg) can only reach 29.02%, 33.93%, 35.00%, 36.00%, 20.33% and 36.19%, respectively, under the same conditions.Carbon nanocages (CNCs) have been synthesized through a simple approach using different alcohols and ferrous oxalate as reactants at 550 °C for 12 h in a sealed autoclave. The lengths of the sides of the CNCs are about 200-350 nm and the wall thicknesses are about 10-15 nm. The formation mechanism of the CNCs is also discussed, based on the experimental results. These CNCs show excellent removal efficiency for phenolic compounds, ammonia, and total particulate matter from cigarette smoke. The adsorption capability of CNCs prepared from ethanol is much higher than that of other samples. For example, the efficiency of 5 mg CNCs (ethanol) for removing the six phenolic compounds p-dihydroxybenzene, m-dihydroxybenzene, o-dihydroxybenzene, phenol, m-cresol, and o-cresol can reach 57.31%, 62.25%, 65.58%, 75.95%, 54.34% and 59.43%, respectively, while that of the commercial activated carbon (5 mg) can only reach 29.02%, 33.93%, 35.00%, 36.00%, 20.33% and 36.19%, respectively, under

  17. LSER model for organic compounds adsorption by single-walled carbon nanotubes: Comparison with multi-walled carbon nanotubes and activated carbon.

    Science.gov (United States)

    Yu, Xiangquan; Sun, Weiling; Ni, Jinren

    2015-11-01

    LSER models for organic compounds adsorption by single and multi-walled carbon nanotubes and activated carbon were successfully developed. The cavity formation and dispersion interactions (vV), hydrogen bond acidity interactions (bB) and π-/n-electron interactions (eE) are the most influential adsorption mechanisms. SWCNTs is more polarizable, less polar, more hydrophobic, and has weaker hydrogen bond accepting and donating abilities than MWCNTs and AC. Compared with SWCNTs and MWCNTs, AC has much less hydrophobic and less hydrophilic adsorption sites. The regression coefficients (e, s, a, b, v) vary in different ways with increasing chemical saturation. Nonspecific interactions (represented by eE and vV) have great positive contribution to organic compounds adsorption, and follow the order of SWCNTs > MWCNTs > AC, while hydrogen bond interactions (represented by aA and bB) demonstrate negative contribution. These models will be valuable for understanding adsorption mechanisms, comparing adsorbent characteristics, and selecting the proper adsorbents for certain organic compounds. PMID:26319510

  18. Stable Carbon Isotope Ratios of Phenolic Compounds in Secondary Particulate Organic Matter Formed by Photooxidation of Toluene

    CERN Document Server

    Irei, Satoshi; Huang, Lin; Auld, Janeen; Collin, Fabrice; Hastie, Donald

    2014-01-01

    Compound-specific stable carbon isotope ratios for phenolic compounds in secondary particulate organic matter (POM) formed by photooxidation of toluene were studied. Secondary POM generated by photooxidation of toluene using a continuous-flow reactor and an 8 cubic meter indoor smog chamber was collected, and then extracted with acetonitrile. Eight phenolic compounds were identified in the extracts by a gas chromatograph coupled with a mass spectrometer, and their compound-specific stable carbon isotope ratios were determined by a gas chromatograph coupled with a combustion furnace followed by an isotope ratio mass spectrometer. The majority of the products, including methylnitrophenols and methylnitrocatechols, were isotopically depleted by 5 to 6 permil compared to the initial isotope ratio for toluene, whereas the isotope ratio for 4_nitrophenol remained the same as the initial isotope ratio for toluene. Based on the reaction mechanisms postulated in literature, stable carbon isotope ratios of these produc...

  19. Effect of effluent organic matter on the adsorption of perfluorinated compounds onto activated carbon

    Energy Technology Data Exchange (ETDEWEB)

    Yu, Jing [State Key Laboratory of Pollution Control and Resource Reuse, School of the Environment, Nanjing University, Nanjing 210046 (China); College of Environmental Science and Engineering, Yangzhou University, 196 West Huayang Road, Yangzhou 225127 (China); Lv, Lu, E-mail: esellu@nju.edu.cn [State Key Laboratory of Pollution Control and Resource Reuse, School of the Environment, Nanjing University, Nanjing 210046 (China); Lan, Pei [State Key Laboratory of Pollution Control and Resource Reuse, School of the Environment, Nanjing University, Nanjing 210046 (China); College of Environmental Science and Engineering, Yangzhou University, 196 West Huayang Road, Yangzhou 225127 (China); Zhang, Shujuan [State Key Laboratory of Pollution Control and Resource Reuse, School of the Environment, Nanjing University, Nanjing 210046 (China); Pan, Bingcai, E-mail: bcpan@nju.edu.cn [State Key Laboratory of Pollution Control and Resource Reuse, School of the Environment, Nanjing University, Nanjing 210046 (China); Zhang, Weiming [State Key Laboratory of Pollution Control and Resource Reuse, School of the Environment, Nanjing University, Nanjing 210046 (China)

    2012-07-30

    Highlights: Black-Right-Pointing-Pointer The presence of EfOM significantly reduced the adsorption capacities and rates of PFCs. Black-Right-Pointing-Pointer Low-molecular-weight EfOM compounds (<1 kDa) compete for adsorption sites of PFSs directly. Black-Right-Pointing-Pointer Large-molecular-weight EfOM compounds (>30 kDa) affect the adsorption through pore blockage or restriction effect. Black-Right-Pointing-Pointer Changes in surface properties of PAC caused by preloaded EfOM could affect PFCs adsorption. - Abstract: Effect of effluent organic matter (EfOM) on the adsorption of perfluorooctane sulfonate (PFOS) and perfluorooctanoate (PFOA) onto powdered activated carbon (PAC) was quantitatively investigated at environmentally relevant concentration levels. The adsorption of both perfluorinated compounds (PFCs) onto PAC followed pseudo-second order kinetics and fitted the Freundlich model well under the given conditions. Intraparticle diffusion was found to be the rate-controlling step in the PFC adsorption process onto PAC in the absence and presence of EfOM. The presence of EfOM, either in PFC-EfOM simultaneous adsorption onto fresh PAC or in PFC adsorption onto EfOM-preloaded PAC, significantly reduced the adsorption capacities and sorption rates of PFCs. The pH of zero point of charge was found to be 7.5 for fresh PAC and 4.2 for EfOM-preloaded PAC, suggesting that the adsorbed EfOM imparted a negative charge on PAC surface. The effect of molecular weight distribution of EfOM on the adsorption of PFCs was investigated with two EfOM fractions obtained by ultrafiltration. The low-molecular-weight compounds (<1 kDa) were found to be the major contributors to the significant reduction in PFC adsorption capacity, while large-molecular-weight compounds (>30 kDa) had much less effect on PFC adsorption capacity.

  20. Resolution of Adsorption and Partition Components of Organic Compounds on Black Carbons.

    Science.gov (United States)

    Chiou, Cary T; Cheng, Jianzhong; Hung, Wei-Nung; Chen, Baoliang; Lin, Tsair-Fuh

    2015-08-01

    Black carbons (BCs) may sequester non-ionic organic compounds by adsorption and/or partition to varying extents. Up to now, no experimental method has been developed to accurately resolve the combined adsorption and partition capacity of a compound on a BC. In this study, a unique "adsorptive displacement method" is introduced to reliably resolve the adsorption and partition components for a solute-BC system. It estimates the solute adsorption on a BC by the use of an adsorptive displacer to displace the adsorbed target solute into the solution phase. The method is validated by tests with uses of activated carbon as the model carbonaceous adsorbent, soil organic matter as the model carbonaceous partition phase, o-xylene and 1,2,3-trichlorobenzene as the reference solutes, and p-nitrophenol as the adsorptive displacer. Thereafter, the adsorption-partition resolution was completed for the two solutes on selected model BCs: four biochars and two National Institute of Standards and Technology (NIST) standard soots (SRM-2975 and SRM-1650b). The adsorption and partition components resolved for selected solutes with given BCs and their dependences upon solute properties enable one to cross-check the sorption data of other solutes on the same BCs. The resolved components also provide a theoretical basis for exploring the potential modes and extents of different solute uptakes by given BCs in natural systems. PMID:26114972

  1. Experimental evaluation of biomass burning emissions: Nitrogen and carbon containing compounds

    International Nuclear Information System (INIS)

    Data are presented on the nitrogen and carbon emissions of biomass burning. The results of the authors' experiments enable them to calculate new source strengths for many compounds, considering different burning stages and fire conditions on the one hand, and different fuel types and properties, on the other hand. They also presented a method for balancing elemental budgets of fires, which had already been described for carbon compounds by other authors but which is new for the nitrogen inventory. Based on their measurements they show that biomass burning contributes significantly to the global budgets of HCN, CH3CN (possibly the major source), NOx (12%), CO(22%), C2 to C4 hydrocarbons (14%), CH3Cl(41%), and probably also to the global source of C1-C5 aliphatic amines. Further, pyrogenic CO2 amounts are likely to represent a substantial contribution to the global greenhouse warming. An important result, from the study is the identification of N2 emissions, which causes a significant loss of fixed nitrogen (pyro-denitrification) in tropical ecosystems in the order of 5% to 20% of the global nitrogen fixation rate. Because of an interesting interplay between an enhanced postfire nitrogen fixation and an enhanced postfire N2O emission, it is not yet known if losses due to pyro-denitrification are balanced by nitrogen fixation

  2. Applications of compound-specific carbon isotope ratios in organic contaminant studies

    International Nuclear Information System (INIS)

    In this paper results are presented on the application of compound-specific isotope ratios measurements to assess biodegradation of chlorinated solvents, in particularly on microbial dechlorination of tetrachloroethene (PCE) and trichloroethene (TCE). Analytical aspects and isotope data from laboratory and field studies are discussed. The analytical tests showed that both headspace and SPME techniques provide accurate δ13C values with a similar precision for a wide range of chlorinated solvents. However, the SPME method is generally more sensitive. The microcosm experiments show that a significant isotopic fractionation occurs during dechlorination of PCE and TCE to ethene. The largest fractionation factors are observed in the steps DCE-VC and VC-Ethene. In general, the δ13C of each dechlorination product was always more negative than the δ13C of the corresponding precursor. In addition, the δ13C values of each compound increased with time. A similar pattern was observed for dechlorination of PCE at a field site. These results show that compound-specific carbon isotope ratios technology is a very sensitive tool for evaluation of natural attenuation of chlorinated solvents in groundwater. (author)

  3. Predicting adsorption of aromatic compounds by carbon nanotubes based on quantitative structure property relationship principles

    Science.gov (United States)

    Rahimi-Nasrabadi, Mehdi; Akhoondi, Reza; Pourmortazavi, Seied Mahdi; Ahmadi, Farhad

    2015-11-01

    Quantitative structure property relationship (QSPR) models were developed to predict the adsorption of aromatic compounds by carbon nanotubes (CNTs). Five descriptors chosen by combining self-organizing map and stepwise multiple linear regression (MLR) techniques were used to connect the structure of the studied chemicals with their adsorption descriptor (K∞) using linear and nonlinear modeling techniques. Correlation coefficient (R2) of 0.99 and root-mean square error (RMSE) of 0.29 for multilayered perceptron neural network (MLP-NN) model are signs of the superiority of the developed nonlinear model over MLR model with R2 of 0.93 and RMSE of 0.36. The results of cross-validation test showed the reliability of MLP-NN to predict the K∞ values for the aromatic contaminants. Molar volume and hydrogen bond accepting ability were found to be the factors much influencing the adsorption of the compounds. The developed QSPR, as a neural network based model, could be used to predict the adsorption of organic compounds by CNTs.

  4. Enhanced separation of Compound Xueshuantong capsule using functionalized carbon nanotubes with cationic surfactant solutions in MEEKC.

    Science.gov (United States)

    Cao, Jun; Li, Ping; Chen, Jue; Tan, Ting; Dai, Han-Bin

    2013-01-01

    A novel additive of multi-walled carbon nanotubes (MWNTs) dispersed with cationic surfactants or mixed cationic/anionic surfactants was used for MEEKC separation of eight phenolic compounds, four glycosides, and one phenanthraquinone. In this context, several parameters affecting MEEKC separation were studied, including the dispersion agents of MWNTs, MWNTs content, oil type, SDS concentration, and the type and concentration of cosurfactant. Compared with conventional MEEKC, the addition of all types of MWNTs dispersions using single or mixed cationic surfactant solutions in running buffers was especially useful for improving the separation of solutes tested, as they influenced the partitioning between the oil droplets and aqueous phase due to the exceptional electrical properties and large surface areas of MWNTs. Use of cationic surfactant-coated MWNTs (6.4 μg/mL) as the additive in a microemulsion buffer (0.5% octanol, 2.8% SDS, 5.8% isopropanol, and 5 mM borate buffer) yielded complete resolution of 13 analytes. The proposed method has been successfully applied for the detection and quantification of the studied compounds in a complex matrix sample (Compound Xueshuantong capsule). PMID:23161282

  5. Electrically Conductive Compounds of Polycarbonate, Liquid Crystalline Polymer, and Multiwalled Carbon Nanotubes

    Directory of Open Access Journals (Sweden)

    Penwisa Pisitsak

    2012-01-01

    Full Text Available A thermotropic liquid crystalline polymer (LCP was blended with polycarbonate (PC and multiwalled carbon nanotube (CNT with the goal of improving electrical conductivity and mechanical properties over PC. The LCP was anticipated to produce fibrillar domains in PC and help improve the mechanical properties. The study was carried out using two grades of LCP—Vectra A950 (VA950 and Vectra V400P (V400P. The compounds contained 20 wt% LCP and 0.5 to 15 wt% CNT. The compounds were prepared by melt-blending in a twin-screw minicompounder and then injection molded using a mini-injection molder. The fibrillar domains of LCP were found only in the case of PC/VA950 blend. However, these fibrils turned into droplets in the presence of CNT. It was found that CNT preferentially remained inside the LCP domains as predicted from the value of spreading coefficient. The electrical conductivity showed the following order with the numbers in parenthesis representing the electrical percolation threshold of the compounds: PC/CNT (1% > PC/VA950P/CNT (1% > PC/V400P/CNT (3%. The storage modulus showed improvements with the addition of CNT and VA950.

  6. Removal of sulfur compounds from petroleum refinery wastewater through adsorption on modified activated carbon.

    Science.gov (United States)

    Ben Hariz, Ichrak; Al Ayni, Foued; Monser, Lotfi

    2014-01-01

    The adsorption of sulfur compounds from petroleum refinery wastewater on a chemically modified activated carbon (MAC) was investigated. The modification technique (nitric acid, hydrogen peroxide and thermal modification) enhanced the removal capacity of carbon and therefore decreases cost-effective removal of sulfide from refinery wastewater. Adsorption equilibrium and kinetics data were determined for sulfur removal from real refinery wastewater. The data were evaluated according to several adsorption isotherm and kinetics models. The Freundlich isotherm fitted well with the equilibrium data of sulfur on different adsorbents, whereas the kinetics data were best fitted by the pseudo-second-order model. Insights of sulfide removal mechanisms indicated that the sorption was controlled through the intraparticle diffusion mechanism with a significant contribution of film diffusion. The MAC adsorbent was found to have an effective removal capacity of approximately 2.5 times that of non-modified carbon. Using different MAC, sulfides were eliminated with a removal capacity of 52 mg g(-1). Therefore, MAC can be utilized as an effective and less expensive adsorbent for the reduction of sulfur in refinery wastewater. PMID:25353943

  7. The removal of endocrine disrupting compounds, pharmaceutically activated compounds and cyanobacterial toxins during drinking water preparation using activated carbon--a review.

    Science.gov (United States)

    Delgado, Luis F; Charles, Philippe; Glucina, Karl; Morlay, Catherine

    2012-10-01

    This paper provides a review of recent scientific research on the removal by activated carbon (AC) in drinking water (DW) treatment of 1) two classes of currently unregulated trace level contaminants with potential chronic toxicity-pharmaceutically activate compounds (PhACs) and endocrine disrupting compounds (EDCs); 2) cyanobacterial toxins (CyBTs), which are a group of highly toxic and regulated compounds (as microcystin-LR); and 3) the above mentioned compounds by the hybrid system powdered AC/membrane filtration. The influence of solute and AC properties, as well as the competitive effect from background natural organic matter on the adsorption of such trace contaminants, are also considered. In addition, a number of adsorption isotherm parameters reported for PhACs, EDCs and CyBTs are presented herein. AC adsorption has proven to be an effective removal process for such trace contaminants without generating transformation products. This process appears to be a crucial step in order to minimize PhACs, EDCs and CyBTs in finished DW, hence calling for further studies on AC adsorption removal of these compounds. Finally, a priority chart of PhACs and EDCs warranting further study for the removal by AC adsorption is proposed based on the compounds' structural characteristics and their low removal by AC compared to the other compounds. PMID:22885596

  8. High Carbon Use Efficiency is Not Explained by Production of Storage Compounds

    Science.gov (United States)

    Dijkstra, Paul; van Groenigen, Kees-Jan

    2015-04-01

    The efficiency with which microbes use substrate to make new microbial biomass (Carbon Use Efficiency or CUE; mol C / mol C) is an important variable in soil and ecosystem C cycling models. Estimates of CUE in soil microbial communities vary widely. It has been hypothesized that high values of CUE are associated with production of storage compounds following a sudden increases in substrate availability during CUE measurements. In that case, these high CUE values would not be representative for balanced microbial growth (i.e. the production of all compounds needed to make new microbial cells). To test this hypothesis, we added position-specific 13C-labeled glucose isotopomers in parallel incubations of a ponderosa pine and piñon-juniper soil. We compared the measured pattern of CO2 release for the six glucose C atoms with patterns of CO2 production expected for balanced growth with a low, medium, or high CUE, and with CO2 production patterns associated with production of storage compounds (glycogen, lipids, or polyhydroxybutyrate). The measured position-specific CO2 production did not match that for production of glycogen, lipids, or polyhydroxybutyrate, but agreed closely with that expected for balanced growth at high CUE and high pentose phosphate pathway activity. We conclude that soil microbial communities utilize glucose substrate for biomass growth with high CUE, and that addition of small amounts of 13C-labeled glucose tracers do not affect CUE or induce storage compounds production. We submit that the measurement of position-specific CO2 production offers a quick and easy way to test biochemically explicit hypotheses concerning microbial growth metabolism.

  9. Rare earths: preparation of spectro chemically pure standards, study of their carbonates and synthesis of a new compound series - the peroxy carbonates

    International Nuclear Information System (INIS)

    In this work the following studies are concerned: I) preparation of lanthanum, cerium, praseodymium, neodymium and samarium oxides for use as spectro chemically pure standards; II) behavior of the rare earth (La, Ce, Pr, Nd, Sm) carbonates soluble in ammonium carbonate and mixture of ammonium carbonate/ammonium hydroxide, and III) synthesis and characterization of rare earth peroxy carbonates - a new series of compounds. Data for the synthesis and characterization of the rare earths peroxy carbonates described for the first time in this work are presented and discussed. With the aid of thermal analysis (TG-DTG) the thermal stability and the stoichiometric composition for new compounds were established and a mechanism of thermal decomposition was proposed. The peroxy carbonate was prepared by the addition of hydrogen peroxyde to the complexed soluble rare earths carbonates. These studies included also the determinations of active oxygen, the total rare earth oxide by gravimetry and complexometry and the C, H and N contents by microanalysis. The new compounds were also investigated by infrared spectroscopy. (author)

  10. Characterization, Quantification and Compound-specific Isotopic Analysis of Pyrogenic Carbon Using Benzene Polycarboxylic Acids (BPCA).

    Science.gov (United States)

    Wiedemeier, Daniel B; Lang, Susan Q; Gierga, Merle; Abiven, Samuel; Bernasconi, Stefano M; Früh-Green, Gretchen L; Hajdas, Irka; Hanke, Ulrich M; Hilf, Michael D; McIntyre, Cameron P; Scheider, Maximilian P W; Smittenberg, Rienk H; Wacker, Lukas; Wiesenberg, Guido L B; Schmidt, Michael W I

    2016-01-01

    Fire-derived, pyrogenic carbon (PyC), sometimes called black carbon (BC), is the carbonaceous solid residue of biomass and fossil fuel combustion, such as char and soot. PyC is ubiquitous in the environment due to its long persistence, and its abundance might even increase with the projected increase in global wildfire activity and the continued burning of fossil fuel. PyC is also increasingly produced from the industrial pyrolysis of organic wastes, which yields charred soil amendments (biochar). Moreover, the emergence of nanotechnology may also result in the release of PyC-like compounds to the environment. It is thus a high priority to reliably detect, characterize and quantify these charred materials in order to investigate their environmental properties and to understand their role in the carbon cycle. Here, we present the benzene polycarboxylic acid (BPCA) method, which allows the simultaneous assessment of PyC's characteristics, quantity and isotopic composition ((13)C and (14)C) on a molecular level. The method is applicable to a very wide range of environmental sample materials and detects PyC over a broad range of the combustion continuum, i.e., it is sensitive to slightly charred biomass as well as high temperature chars and soot. The BPCA protocol presented here is simple to employ, highly reproducible, as well as easily extendable and modifiable to specific requirements. It thus provides a versatile tool for the investigation of PyC in various disciplines, ranging from archeology and environmental forensics to biochar and carbon cycling research. PMID:27214064

  11. Characterization, Quantification and Compound-specific Isotopic Analysis of Pyrogenic Carbon Using Benzene Polycarboxylic Acids (BPCA)

    Science.gov (United States)

    Wiedemeier, Daniel B.; Lang, Susan Q.; Gierga, Merle; Abiven, Samuel; Bernasconi, Stefano M.; Früh-Green, Gretchen L.; Hajdas, Irka; Hanke, Ulrich M.; Hilf, Michael D.; McIntyre, Cameron P.; Scheider, Maximilian P. W.; Smittenberg, Rienk H.; Wacker, Lukas; Wiesenberg, Guido L. B.; Schmidt, Michael W. I.

    2016-01-01

    Fire-derived, pyrogenic carbon (PyC), sometimes called black carbon (BC), is the carbonaceous solid residue of biomass and fossil fuel combustion, such as char and soot. PyC is ubiquitous in the environment due to its long persistence, and its abundance might even increase with the projected increase in global wildfire activity and the continued burning of fossil fuel. PyC is also increasingly produced from the industrial pyrolysis of organic wastes, which yields charred soil amendments (biochar). Moreover, the emergence of nanotechnology may also result in the release of PyC-like compounds to the environment. It is thus a high priority to reliably detect, characterize and quantify these charred materials in order to investigate their environmental properties and to understand their role in the carbon cycle. Here, we present the benzene polycarboxylic acid (BPCA) method, which allows the simultaneous assessment of PyC's characteristics, quantity and isotopic composition (13C and 14C) on a molecular level. The method is applicable to a very wide range of environmental sample materials and detects PyC over a broad range of the combustion continuum, i.e., it is sensitive to slightly charred biomass as well as high temperature chars and soot. The BPCA protocol presented here is simple to employ, highly reproducible, as well as easily extendable and modifiable to specific requirements. It thus provides a versatile tool for the investigation of PyC in various disciplines, ranging from archeology and environmental forensics to biochar and carbon cycling research. PMID:27214064

  12. Liquid-phase adsorption of multi-ring thiophenic sulfur compounds on carbon materials with different surface properties.

    Science.gov (United States)

    Zhou, Anning; Ma, Xiaoliang; Song, Chunshan

    2006-03-16

    This work examines the effects of structural and surface properties of carbon materials on the adsorption of benzothiophene (BT), dibenzothiophene (DBT), 4-methyldibenzothiophene (4-MDBT) and 4,6-dimethyl-dibenzothiophene (4,6-DMDBT) in the presence of 10 wt % of aromatics in liquid alkanes that simulate sulfur compounds in diesel fuels. The equilibrium-adsorption capacity varies significantly, from 1.7 to 7.0 mg-S/g-A. The results show that different carbon materials have significantly different sulfur-adsorption capacities and selectivities that depend not only on textural structure but also on surface functional groups. The adsorption of multi-ring sulfur compounds on carbon materials was found to obey the Langmuir isotherm. On the basis of adsorption tests and the characterization of carbon materials by BET and XPS, the oxygen-containing functional groups on the surface appear to play an important role in increasing sulfur-adsorption capacity. The adsorption-selectivity trend of the carbon materials for various compounds increases in the order of BT adsorption over nickel-based adsorbents. The regeneration of spent activated carbons was also conducted by solvent washing. The high-adsorption capacity and selectivity for methyl DBTs indicate that certain activated carbons are promising adsorbents for selective adsorption for removing sulfur (SARS) as a new approach to ultra deep desulfurization of diesel fuels. PMID:16526705

  13. RT-MATRIX: Measuring Total Organic Carbon by Photocatalytic Oxidation of Volatile Organic Compounds

    Science.gov (United States)

    2008-01-01

    Volatile organic compounds (VOCs) inevitably accumulate in enclosed habitats such as the International Space Station and the Crew Exploration Vehicle (CEV) as a result of human metabolism, material off-gassing, and leaking equipment. Some VOCs can negatively affect the quality of the crew's life, health, and performance; and consequently, the success of the mission. Air quality must be closely monitored to ensure a safe living and working environment. Currently, there is no reliable air quality monitoring system that meets NASA's stringent requirements for power, mass, volume, or performance. The ultimate objective of the project -- the development of a Real-Time, Miniaturized, Autonomous Total Risk Indicator System (RT.MATRIX).is to provide a portable, dual-function sensing system that simultaneously determines total organic carbon (TOC) and individual contaminants in air streams.

  14. The Synthesis of Imidazoline Derivative Compounds as Corrosion Inhibitor towards Carbon Steel in 1% NaCl Solution

    Directory of Open Access Journals (Sweden)

    Deana Wahyuningrum

    2008-03-01

    Full Text Available Oleic imidazoline is one of the nitrogen containing heterocyclic compounds that has been widely used as commercial corrosion inhibitor, especially in minimizing the carbon dioxide induced corrosion process in oilfield mining. In this present work, some imidazoline derivative compounds have been synthesized utilizing both conventional and microwave assisted organic synthesis (MAOS methods, in order to determine their corrosion inhibition properties on carbon steel surface. The MAOS method is more effective in synthesizing these compounds than the conventional method regarding to the higher chemical yields of products (91% to 94% and the shorter reaction times (7 to 10 minutes. The characterization of corrosion inhibition activities of the synthesized products towards carbon steel in 1% NaCl solution was determined by the Tafel plot method. The corrosion inhibition activities of compound 1b ((Z-2-(2-(heptadec-8-enyl-4,5-dihydroimidazol-1-ylethanamine, 2b ((Z-2-(2-(heptadec-8-enyl-4,5-dihydroimidazol-1-ylethanol and 3b (2-(2-heptadecyl-4,5-dihydroimidazol-1-ylethanamine at 8 ppm concentration in 1% NaCl solution are, respectively, 32.18%, 39.59% and 12.73%. The heptadec-8-enyl and hydroxyethyl substituents at C(2 and N(1 position of imidazoline ring, respectively, gave the most effective corrosion inhibition activity towards carbon steel compared to the presence of other substituents. The increase in concentrations of compound 1b, 2b and 3b in 1% NaCl solution tends to improve their corrosion inhibition activities. Based on the analysis of the free Gibbs adsorption energy (DG0ads values of compound 1b, 2b and 3b (-32.97, -34.34 and -31.27 kJ/mol, respectively, these compounds have the potential to interact with carbon steel through semi-physiosorption or semi-chemisorption.

  15. Local Field Effects in the Energy Transfer between a Chromophore and a Carbon Nanotube : a Single Nano-compound Investigation.

    OpenAIRE

    Roquelet, Cyrielle; Vialla, Fabien; Diederichs, Carole; Roussignol, Philippe; Delalande, Claude; Deleporte, Emmanuelle; Lauret, Jean-Sébastien; Voisin, Christophe

    2012-01-01

    Energy transfer in non-covalently bound porphyrin / carbon nanotube compounds is investigated at the single nano-compound scale. Excitation spectroscopy of the luminescence of the nanotube shows two resonances arising from intrinsic excitation of the nanotube and from energy transfer from the porphyrin. Polarization diagrams show that both resonances are highly anisotropic with a preferred direction along the tube axis. The energy transfer is thus strongly anisotropic despite the almost isotr...

  16. Adsorption of volatile sulphur compounds onto modified activated carbons: effect of oxygen functional groups.

    Science.gov (United States)

    Vega, Esther; Lemus, Jesús; Anfruns, Alba; Gonzalez-Olmos, Rafael; Palomar, José; Martin, María J

    2013-08-15

    The effect of physical and chemical properties of activated carbon (AC) on the adsorption of ethyl mercaptan, dimethyl sulphide and dimethyl disulphide was investigated by treating a commercial AC with nitric acid and ozone. The chemical properties of ACs were characterised by temperature programme desorption and X-ray photoelectron spectroscopy. AC treated with nitric acid presented a larger amount of oxygen functional groups than materials oxidised with ozone. This enrichment allowed a significant improvement on adsorption capacities for ethyl mercaptan and dimethyl sulphide but not for dimethyl disulphide. In order to gain a deeper knowledge on the effect of the surface chemistry of AC on the adsorption of volatile sulphur compounds, the quantum-chemical COSMO-RS method was used to simulate the interactions between AC surface groups and the studied volatile sulphur compounds. In agreement with experimental data, this model predicted a greater affinity of dimethyl disulphide towards AC, unaffected by the incorporation of oxygen functional groups in the surface. Moreover, the model pointed out to an increase of the adsorption capacity of AC by the incorporation of hydroxyl functional groups in the case of ethyl mercaptan and dimethyl sulphide due to the hydrogen bond interactions. PMID:23708449

  17. Effect of effluent organic matter on the adsorption of perfluorinated compounds onto activated carbon.

    Science.gov (United States)

    Yu, Jing; Lv, Lu; Lan, Pei; Zhang, Shujuan; Pan, Bingcai; Zhang, Weiming

    2012-07-30

    Effect of effluent organic matter (EfOM) on the adsorption of perfluorooctane sulfonate (PFOS) and perfluorooctanoate (PFOA) onto powdered activated carbon (PAC) was quantitatively investigated at environmentally relevant concentration levels. The adsorption of both perfluorinated compounds (PFCs) onto PAC followed pseudo-second order kinetics and fitted the Freundlich model well under the given conditions. Intraparticle diffusion was found to be the rate-controlling step in the PFC adsorption process onto PAC in the absence and presence of EfOM. The presence of EfOM, either in PFC-EfOM simultaneous adsorption onto fresh PAC or in PFC adsorption onto EfOM-preloaded PAC, significantly reduced the adsorption capacities and sorption rates of PFCs. The pH of zero point of charge was found to be 7.5 for fresh PAC and 4.2 for EfOM-preloaded PAC, suggesting that the adsorbed EfOM imparted a negative charge on PAC surface. The effect of molecular weight distribution of EfOM on the adsorption of PFCs was investigated with two EfOM fractions obtained by ultrafiltration. The low-molecular-weight compounds (30kDa) had much less effect on PFC adsorption capacity. PMID:22609392

  18. Supercritical Carbon Dioxide and Microwave-Assisted Extraction of Functional Lipophilic Compounds from Arthrospira platensis

    Directory of Open Access Journals (Sweden)

    Diego A. Esquivel-Hernández

    2016-05-01

    Full Text Available Arthrospira platensis biomass was used in order to obtain functional lipophilic compounds through green extraction technologies such as supercritical carbon dioxide fluid extraction (SFE and microwave-assisted extraction (MAE. The temperature (T factor was evaluated for MAE, while for SFE, pressure (P, temperature (T, and co-solvent (ethanol (CS were evaluated. The maximum extraction yield of the obtained oleoresin was (4.07% ± 0.14% and (4.27% ± 0.10% for SFE and MAE, respectively. Extracts were characterized by gas chromatography mass spectrometry (GC-MS and gas chromatography flame ionization detector (GC-FID. The maximum contents of functional lipophilic compounds in the SFE and MAE extracts were: for carotenoids 283 ± 0.10 μg/g and 629 ± 0.13 μg/g, respectively; for tocopherols 5.01 ± 0.05 μg/g and 2.46 ± 0.09 μg/g, respectively; and for fatty acids 34.76 ± 0.08 mg/g and 15.88 ± 0.06 mg/g, respectively. In conclusion, the SFE process at P 450 bar, T 60 °C and CS 53.33% of CO2 produced the highest yield of tocopherols, carotenoids and fatty acids. The MAE process at 400 W and 50 °C gives the best extracts in terms of tocopherols and carotenoids. For yield and fatty acids, the MAE process at 400 W and 70 °C produced the highest values. Both SFE and MAE showed to be suitable green extraction technologies for obtaining functional lipophilic compounds from Arthrospira platensis.

  19. Supercritical Carbon Dioxide and Microwave-Assisted Extraction of Functional Lipophilic Compounds from Arthrospira platensis

    Science.gov (United States)

    Esquivel-Hernández, Diego A.; López, Víctor H.; Rodríguez-Rodríguez, José; Alemán-Nava, Gibrán S.; Cuéllar-Bermúdez, Sara P.; Rostro-Alanis, Magdalena; Parra-Saldívar, Roberto

    2016-01-01

    Arthrospira platensis biomass was used in order to obtain functional lipophilic compounds through green extraction technologies such as supercritical carbon dioxide fluid extraction (SFE) and microwave-assisted extraction (MAE). The temperature (T) factor was evaluated for MAE, while for SFE, pressure (P), temperature (T), and co-solvent (ethanol) (CS) were evaluated. The maximum extraction yield of the obtained oleoresin was (4.07% ± 0.14%) and (4.27% ± 0.10%) for SFE and MAE, respectively. Extracts were characterized by gas chromatography mass spectrometry (GC-MS) and gas chromatography flame ionization detector (GC-FID). The maximum contents of functional lipophilic compounds in the SFE and MAE extracts were: for carotenoids 283 ± 0.10 μg/g and 629 ± 0.13 μg/g, respectively; for tocopherols 5.01 ± 0.05 μg/g and 2.46 ± 0.09 μg/g, respectively; and for fatty acids 34.76 ± 0.08 mg/g and 15.88 ± 0.06 mg/g, respectively. In conclusion, the SFE process at P 450 bar, T 60 °C and CS 53.33% of CO2 produced the highest yield of tocopherols, carotenoids and fatty acids. The MAE process at 400 W and 50 °C gives the best extracts in terms of tocopherols and carotenoids. For yield and fatty acids, the MAE process at 400 W and 70 °C produced the highest values. Both SFE and MAE showed to be suitable green extraction technologies for obtaining functional lipophilic compounds from Arthrospira platensis. PMID:27164081

  20. Compound specific radiocarbon analyses to apportion sources of combustion products in sedimentary pyrogenic carbon deposits

    Science.gov (United States)

    Hanke, Ulrich M.; Schmidt, Michael W. I.; McIntyre, Cameron P.; Reddy, Christopher M.; Wacker, Lukas; Eglinton, Timothy I.

    2016-04-01

    Pyrogenic carbon (PyC) is a collective term for carbon-rich residues comprised of a continuum of products generated during biomass burning and fossil fuel combustion. PyC is a key component of the global carbon cycle due to its slow intrinsic decomposition rate and its ubiquity in the environment. It can originate from natural or anthropogenic vegetation fires, coal mining, energy production, industry and transport. Subsequently, PyC can be transported over long distances by wind and water and can eventually be buried in sediments. Information about the origin of PyC (biomass burning vs. fossil fuel combustion) deposited in estuarine sediments is scarce. We studied the highly anoxic estuarine sediments of the Pettaquamscutt River (Rhode Island, U.S.) in high temporal resolution over 250 years and found different combustion proxies reflect local and regional sources of PyC (Hanke et al. in review; Lima et al. 2003). The polycyclic aromatic hydrocarbons (PAH) originate from long-range atmospheric transport, whereas bulk PyC, detected as benzene polycarboxylic acids (BPCA), mainly stems from local catchment run-off. However, to unambiguously apportion PyC sources, we need additional information, such as compound specific radiocarbon (14C) measurements. We report 14C data for individual BPCA including error analysis and for combustion-related PAH. First results indicate that biomass burning is the main source of PyC deposits, with additional minor contributions from fossil fuel combustion. References Hanke U.M., T.I. Eglinton, A.L.L. Braun, C. Reddy, D.B. Wiedemeier, M.W.I. Schmidt. Decoupled sedimentary records of combustion: causes and implications. In review. Lima, A. L.; Eglinton, T. I.; Reddy, C. M., High-resolution record of pyrogenic polycyclic aromatic hydrocarbon deposition during the 20th century. ES&T, 2003, 37 (1), 53-61.

  1. Carbon nanostructures as catalytic support for chemiluminescence of sulfur compounds in a molecular emission cavity analysis system.

    Science.gov (United States)

    Safavi, Afsaneh; Maleki, Norouz; Doroodmand, Mohammad Mahdi; Koleini, Mohammad Mehdi

    2009-06-30

    The effect of different substrates including stainless steel, activated carbon, single-walled carbon nanotubes (SWCNTs), multi-walled carbon nanotubes (MWCNTs), fullerenes (C60, C70, etc.) and SWCNTs doped with iron and palladium nanoparticles were compared for catalytic chemiluminescence reaction of sulfur compounds in a flame-containing cavity of molecular emission cavity analysis (MECA) system. Different forms of CNT substrates were fabricated using electric arc-discharge method. The blue emission of excited S2 was monitored using a CCD camera. The results demonstrate that, due to the high surface area, plenty of basal planes, high thermal conductivity, and high flexibility of the carbon nanostructure as appropriate support, carbon nanostructures play an important role in catalytic chemiluminescence emission of sulfur compounds in MECA. Moreover, the presence of metallic nanoparticles doped on carbon nanostructures enhances their catalytic effect. The results revealed that under similar conditions, SWCNTs/Pd doped nanoparticles, SWCNTs/Fe doped nanoparticles, SWCNTs, MWCNTs and fullerenes have the most catalytic effects on chemiluminescence of sulfur compounds, respectively. PMID:19463563

  2. Activation of the carbon-fluorine bonds in coordination compounds; Activacion de enlaces carbon-fluor en compuestos de coordinacion

    Energy Technology Data Exchange (ETDEWEB)

    Torrens, H. [Universidad Nacional Autonoma de Mexico, Facultad de Quimica, 04510 Mexico D.F. (Mexico)

    2000-07-01

    Activation of the carbon-fluorine bond is of upmost importance in several chemical processes. In search of synthetic alternatives to promote C-F bond cleavage in arylic systems, several square planar palladium and platinum compounds bearing fluorothiolates and fluorophosphines have been studied. In this paper molecular structures are shown for the following compounds trans-((SC{sub 6}F{sub 5})(P(C{sub 6}F{sub 5}){sub 2}(C{sub 6}H{sub 5}))(Pd({mu}-SC{sub 6}F{sub 5}){sub 2} Pd(SC{sub 6}F{sub 5})(P(C{sub 6}F{sub 5}){sub 2} (C{sub 6}H{sub 5})), cis ((SC{sub 6}F{sub 5}) P(C{sub 6}F{sub 5}){sub 2} (C{sub 6}H{sub 5}) Pt({mu}-SC{sub 6}F{sub 5}){sub 2} Pt(SC{sub 6}F{sub 5}) P(C{sub 6}F{sub 5}){sub 2} (C{sub 6}H{sub 5})), trans Pd ({mu}-SC{sub 6}F{sub 5}){sub 2} Pt(SC{sub 6}F{sub 5})(P(C{sub 6}F{sub 5})(C{sub 6}H{sub 5}){sub 2})), Pt (SC{sub 6}F{sub 5}){sub 2} (C{sub 6}F{sub 5}SC{sub 6}F{sub 4} P(C{sub 6}H{sub 5}){sub 2}))((SC{sub 6}F{sub 5}){sub 2} Pt ({mu}-(SC{sub 6}F{sub 5}){sub 2} Pt(SC{sub 6}F{sub 5}){sub 2}){sup 2-} , (SC{sub 6}HF{sub 4}){sub 2} Pt({mu}-SC{sub 6}HF{sub 4}){sub 2} Pt(SC{sub 6}HF{sub 4}){sub 2}){sup 2-} and ((SC{sub 6}F{sub 4}CF{sub 3}-4){sub 2} Pt (SC{sub 6}F{sub 4}CF{sub 3}-4){sub 2}){sup 2-} . (Author)

  3. Analysis of hydrogen, carbon, sulfur and volatile compounds in (U{sub 3}Si{sub 2} - Al) nuclear fuel

    Energy Technology Data Exchange (ETDEWEB)

    Moura, Sergio C.; Redigolo, Marcelo M.; Amaral, Priscila O.; Leao, Claudio; Oliveira, Glaucia A.C. de; Bustillos, Oscar V., E-mail: ovega@ipen.br [Instituto de Pesquisas Energeticas e Nucleares (IPEN/CNEN-SP), Sao Paulo, SP (Brazil)

    2015-07-01

    Uranium silicide U{sub 3}Si{sub 2} is used as nuclear fuel in the research nuclear reactor IEA-R1 at IPEN/CNEN, Sao Paulo, Brazil. The U{sub 3}Si{sub 2} is dispersed in aluminum reaching high densities of uranium in the nucleus of the fuel, up to 4.8 gU cm{sup -3}. This nuclear fuel must comply with a quality control, which includes analysis of hydrogen, carbon and sulfur for the U{sub 3}Si{sub 2} and volatile compound for the aluminum. Hydrogen, carbon and sulfur are analyzed by the method of Radio Frequency gas extraction combustion coupled with Infrared detector. Volatile compounds are analyzed by the method of heated gas extraction coupled with gravimetric measurement. These methods are recommended by the American Society for Testing Materials (ASTM) for nuclear materials. The average carbon and sulfur measurements are 30 μg g{sup -1} and 3 μg g{sup -1}, respectively, and 40 μg g{sup -1} for volatile compounds. The hydrogen analyzer is a TCHEN 600 LECO, carbon and sulfur analyzer is a CS 244 LECO and the volatile compounds analyzer is a home-made apparatus that use a resistant furnace, a gas pipe measurement and a glove-box with controlled atmosphere where an analytical balance has been installed, this analyzer was made at IPEN laboratory. (author)

  4. Photocatalytic and chemical oxidation of organic compounds in supercritical carbon dioxide. 1998 annual progress report

    International Nuclear Information System (INIS)

    'This report summarizes the results of work done during the first 1.3 years of a three year project. During the first nine months effort focussed on the design, construction and testing of a closed recirculating system that can be used to study photochemistry in supercritical carbon dioxide at pressures up to 5,000 psi and temperatures up to about 50 C. This was followed by a period of work in which the photocatalytic oxidation of benzene and acetone in supercritical, liquid, and gaseous carbon dioxide containing dissolved oxygen was demonstrated. The photocatalyst was titanium dioxide supported on glass spheres. This was the first time it was possible to observe photocatalytic oxidation in a supercritical fluid and to compare reaction in the three fluid phases of a solvent. This also demonstrated that it is possible to purify supercritical and liquid carbon dioxide using photochemical oxidation with no chemical additions other than oxygen. The oxidation of benzene produced no intermediates detectable using on line spectroscopic analysis or by gas chromatographic analysis of samples taken from the flow system. The catalyst surface did darken as the reaction proceeded indicating that oxidation products were accumulating on the surface. This is analogous to the behavior of aromatic compounds in air phase photocatalytic oxidation. The reaction of acetone under similar conditions resulted in the formation of low levels of by-products. Two were identified as products of the reaction of acetone with itself (4-methyl-3-penten-2-one and 4-hydroxy-4-methyl-2-pentanone) using gas chromatography with a mass spectrometer detector. Two other by-products also appear to be from the self-reaction of acetone. By-products of this type had not been observed in prior studies of the gas-phase photocatalytic oxidation of acetone. The by-products that have been observed can also be oxidized under the treatment conditions. The above results establish that photocatalytic oxidation of

  5. Adsorption of volatile sulphur compounds onto modified activated carbons: Effect of oxygen functional groups

    International Nuclear Information System (INIS)

    Highlights: • HNO3 oxidation incorporates a higher amount of functionalities than O3 oxidation. • The loss of porosity is compensated by the massive incorporation of oxygen groups. • HNO3 oxidation increases OH groups in AC and the ETM and DMS adsorption capacities. • The oxygen functional groups in the AC surface did not affect the DMDS adsorption. • COSMO-RS predicts the important role of OH groups for VSC adsorption. -- Abstract: The effect of physical and chemical properties of activated carbon (AC) on the adsorption of ethyl mercaptan, dimethyl sulphide and dimethyl disulphide was investigated by treating a commercial AC with nitric acid and ozone. The chemical properties of ACs were characterised by temperature programme desorption and X-ray photoelectron spectroscopy. AC treated with nitric acid presented a larger amount of oxygen functional groups than materials oxidised with ozone. This enrichment allowed a significant improvement on adsorption capacities for ethyl mercaptan and dimethyl sulphide but not for dimethyl disulphide. In order to gain a deeper knowledge on the effect of the surface chemistry of AC on the adsorption of volatile sulphur compounds, the quantum-chemical COSMO-RS method was used to simulate the interactions between AC surface groups and the studied volatile sulphur compounds. In agreement with experimental data, this model predicted a greater affinity of dimethyl disulphide towards AC, unaffected by the incorporation of oxygen functional groups in the surface. Moreover, the model pointed out to an increase of the adsorption capacity of AC by the incorporation of hydroxyl functional groups in the case of ethyl mercaptan and dimethyl sulphide due to the hydrogen bond interactions

  6. Carbon based secondary compounds do not provide protection against heavy metal road pollutants in epiphytic macrolichens.

    Science.gov (United States)

    Gauslaa, Yngvar; Yemets, Olena A; Asplund, Johan; Solhaug, Knut Asbjørn

    2016-01-15

    Lichens are useful monitoring organisms for heavy metal pollution. They are high in carbon based secondary compounds (CBSCs) among which some may chelate heavy metals and thus increase metal accumulation. This study quantifies CBSCs in four epiphytic lichens transplanted for 6months on stands along transects from a highway in southern Norway to search for relationships between concentrations of heavy metals and CBSCs along a gradient in heavy metal pollutants. Viability parameters and concentrations of 21 elements including nutrients and heavy metals in these lichen samples were reported in a separate paper. Medullary CBSCs in fruticose lichens (Ramalina farinacea, Usnea dasypoga) were reduced in the most polluted sites, but not in foliose ones (Parmelia sulcata, Lobaria pulmonaria), whereas cortical CBSC did not change with distance from the road in any species. Strong positive correlations only occurred between the major medullary compound stictic acid present in L. pulmonaria and most heavy metals, consistent with a chelating role of stictic acid, but not of other studied CBSCs or in other species. However, heavy metal chelating did not protect L. pulmonaria against damage because this species experienced the strongest reduction in viability in the polluted sites. CBSCs with an accumulation potential for heavy metals should be quantified in lichen biomonitoring studies of heavy metals because they, like stictic acid, could overshadow pollutant inputs in some species rendering biomonitoring data less useful. In the two fruticose lichen species, CBSCs decreased with increasing heavy metal concentration, probably because heavy metal exposure impaired secondary metabolism. Thus, we found no support for a heavy metal protection role of any CBSCs in studied epiphytic lichens. No intraspecific relationships occurred between CBSCs versus N or C/N-ratio. Interspecifically, medullary CBSCs decreased and cortical CBSCs increased with increasing C/N-ratio. PMID:26437350

  7. An accurate benchmark description of the interactions between carbon dioxide and polyheterocyclic aromatic compounds containing nitrogen.

    Science.gov (United States)

    Li, Sicheng; Smith, Daniel G A; Patkowski, Konrad

    2015-07-01

    We assessed the performance of a large variety of modern density functional theory approaches for the adsorption of carbon dioxide on molecular models of pyridinic N-doped graphene. Specifically, we selected eight polyheterocyclic aromatic compounds ranging from pyridine and pyrazine to 1,6-diazacoronene and investigated their complexes with CO2 for a large range of intermolecular distances and including both in-plane and stacked orientations. The benchmark interaction energies were computed at the complete-basis-set limit MP2 level plus a CCSD(T) coupled-cluster correction in a moderate but carefully selected basis set. Using a set of 96 benchmark CCSD(T)-level interaction energies as a reference, we investigated the accuracy of DFT-based approaches as a function of the density functional, the dispersion correction, the basis set, and the counterpoise correction or lack thereof. While virtually all DFT variants exhibit some deterioration of accuracy for distances slightly shorter than the van der Waals minima, we were able to identify several schemes such as B2PLYP-D3 and M05-2X-D3 whose average errors on the entire benchmark data set are in the 5-10% range. The top DFT performers were subsequently used to investigate the energy profile for a carbon dioxide transition through model N-doped graphene pores. All investigated methods confirmed that the largest, N4H4 pore allows for a barrierless CO2 transition to the other side of a graphene sheet. PMID:26055458

  8. Predicting trace organic compound breakthrough in granular activated carbon using fluorescence and UV absorbance as surrogates.

    Science.gov (United States)

    Anumol, Tarun; Sgroi, Massimiliano; Park, Minkyu; Roccaro, Paolo; Snyder, Shane A

    2015-06-01

    This study investigated the applicability of bulk organic parameters like dissolved organic carbon (DOC), UV absorbance at 254 nm (UV254), and total fluorescence (TF) to act as surrogates in predicting trace organic compound (TOrC) removal by granular activated carbon in water reuse applications. Using rapid small-scale column testing, empirical linear correlations for thirteen TOrCs were determined with DOC, UV254, and TF in four wastewater effluents. Linear correlations (R(2) > 0.7) were obtained for eight TOrCs in each water quality in the UV254 model, while ten TOrCs had R(2) > 0.7 in the TF model. Conversely, DOC was shown to be a poor surrogate for TOrC breakthrough prediction. When the data from all four water qualities was combined, good linear correlations were still obtained with TF having higher R(2) than UV254 especially for TOrCs with log Dow>1. Excellent linear relationship (R(2) > 0.9) between log Dow and the removal of TOrC at 0% surrogate removal (y-intercept) were obtained for the five neutral TOrCs tested in this study. Positively charged TOrCs had enhanced removals due to electrostatic interactions with negatively charged GAC that caused them to deviate from removals that would be expected with their log Dow. Application of the empirical linear correlation models to full-scale samples provided good results for six of seven TOrCs (except meprobamate) tested when comparing predicted TOrC removal by UV254 and TF with actual removals for GAC in all the five samples tested. Surrogate predictions using UV254 and TF provide valuable tools for rapid or on-line monitoring of GAC performance and can result in cost savings by extended GAC run times as compared to using DOC breakthrough to trigger regeneration or replacement. PMID:25792436

  9. Predicting trace organic compound attenuation with spectroscopic parameters in powdered activated carbon processes.

    Science.gov (United States)

    Ziska, Austin D; Park, Minkyu; Anumol, Tarun; Snyder, Shane A

    2016-08-01

    The removal of trace organic compounds (TOrCs) is of growing interest in water research and society. Powdered activated carbon (PAC) has been proven to be an effective method of removal for TOrCs in water, with the degree of effectiveness depending on dosage, contact time, and activated carbon type. In this study, the attenuation of TOrCs in three different secondary wastewater effluents using four PAC materials was studied in order to elucidate the effectiveness and efficacy of PAC for TOrC removal. With the notable exception of hydrochlorothiazide, all 14 TOrC indicators tested in this study exhibited a positive correlation of removal rate with their log Dow values, demonstrating that the main adsorption mechanism was hydrophobic interaction. As a predictive model, the modified Chick-Watson model, often used for the prediction of microorganism inactivation by disinfectants, was applied. The applied model exhibited good predictive power for TOrC attenuation by PAC in wastewater. In addition, surrogate models based upon spectroscopic measurements including UV absorbance at 254 nm and total fluorescence were applied to predict TOrC removal by PAC. The surrogate model was found to provide an excellent prediction of TOrC attenuation for all combinations of water quality and PAC type included in this study. The success of spectrometric parameters as surrogates in predicting TOrC attenuation by PAC are particularly useful because of their potential application in real-time on-line sensor monitoring and process control at full-scale water treatment plants, which could lead to significantly reduced operator response times and PAC operational optimization. PMID:27174829

  10. Anomalous hydrogen absorption on non-stoichiometric iron-carbon compound

    International Nuclear Information System (INIS)

    Research highlights: → CnanoHx with Fe showed the characteristic hydrogen storage properties. → Anomalous hydrogen absorption on non-stoichiometric Fe-C was clarified. → More than 10 mass% of hydrogen was absorbed in the Fe-C phase. - Abstract: On the synthesis of nano-structural hydrogenated graphite by ball-milling under H2 atmosphere, iron contamination was mingled from steel balls during ball-milling. It is clarified by spectroscopic measurements that the mingled iron formed a non-stoichiometric iron-carbon (Fe-C) compound. The Fe-C phase was transformed to a well-ordered phase with H2 desorption at 450 oC, suggesting that the hydrogen atoms were anomalously trapped at the Fe-C phase. With respect to hydrogen absorbing properties, the mingled iron enhanced the hydrogen capacity by about 50% compared with iron free hydrogenated graphite, where H/Fe was about 13 mass%. Therefore, if the hydrogen absorption site originated in the Fe-C phase could be synthesized independently, it should be recognized as a promising hydrogen storage system.

  11. Supercritical Carbon Dioxide Extraction of Bioactive Compounds from Ampelopsis grossedentata Stems: Process Optimization and Antioxidant Activity

    Directory of Open Access Journals (Sweden)

    Da Sun

    2011-10-01

    Full Text Available Supercritical carbon dioxide (SC-CO2 extraction of bioactive compounds including flavonoids and phenolics from Ampelopsis grossedentata stems was carried out. Extraction parameters such as pressure, temperature, dynamic time and modifier, were optimized using an orthogonal array design of L9 (34, and antioxidant activities of the extracts were evaluated by 2,2-diphenyl-1-picrylhydrazyl (DPPH free radical scavenging assay and ferrous ion chelating (FIC assay. The best conditions obtained for SC-CO2 extraction of flavonoids was 250 bar, 40 °C, 50 min, and with a modifier of methanol/ethanol (1:3, v/v, and that for phenolics extraction was 250 bar, 40 °C, 50 min, and with a modifier of methanol/ethanol (1:1, v/v. Meantime, flavonoids and phenolics were found to be mainly responsible for the DPPH scavenging activity of the extracts, but not for the chelating activity on ferrous ion according to Pearson correlation analysis. Furthermore, several unreported flavonoids such as apigenin, vitexin, luteolin, etc., have been detected in the extracts from A. grossedentata stems.

  12. Electrochemical detection of phenolic estrogenic compounds at clay modified carbon paste electrode

    Science.gov (United States)

    Belkamssa, N.; Ouattara, L.; Kawachi, A.; Tsujimura, M.; Isoda, H.; Chtaini, A.; Ksibi, M.

    2015-04-01

    A simple and sensitive electroanalytical method was developed to determine the Endocrine Disrupting chemical 4-tert-octylphenol on clay modified carbon paste electrode (Clay/CPE). The electrochemical response of the proposed electrode was studied by means of cyclic and square wave voltammetry. It has found that the oxidation of 4-tert-octylphenol on the clay/CPE displayed a well-defined oxidation peak. Under these optimal conditions, a linear relation between concentrations of 4-tert-octylphenol current response was obtained over range of 7.26×10-6 to 3.87×10-7 with a detection and quantification limit of 9.2×10-7 M and 3.06×10-6 M, respectively. The correlation coefficient is 0.9963. The modified electrode showed suitable sensitivity, high stability and an accurate detection of 4-tert-octylphenol. The modified electrode also relevant suitable selectivity for various phenolic estrogenic compounds.

  13. Quantification of biogenic volatile organic compounds with a flame ionization detector using the effective carbon number concept

    Science.gov (United States)

    Faiola, C. L.; Erickson, M. H.; Fricaud, V. L.; Jobson, B. T.; VanReken, T. M.

    2012-08-01

    Biogenic volatile organic compounds (BVOCs) are emitted into the atmosphere by plants and include isoprene, monoterpenes, sesquiterpenes, and their oxygenated derivatives. These BVOCs are among the principal factors influencing the oxidative capacity of the atmosphere in forested regions. BVOC emission rates are often measured by collecting samples onto adsorptive cartridges in the field and then transporting these samples to the laboratory for chromatographic analysis. One of the most commonly used detectors in chromatographic analysis is the flame ionization detector (FID). For quantitative analysis with an FID, relative response factors may be estimated using the effective carbon number (ECN) concept. The purpose of this study was to determine the ECN for a variety of terpenoid compounds to enable improved quantification of BVOC measurements. A dynamic dilution system was developed to make quantitative gas standards of VOCs with mixing ratios from 20-55 ppb. For each experiment using this system, one terpene standard was co-injected with an internal reference, n-octane, and analyzed via an automated cryofocusing system interfaced to a gas chromatograph flame ionization detector and mass spectrometer (GC/MS/FID). The ECNs of 16 compounds (14 BVOCs) were evaluated with this approach, with each test compound analyzed at least three times. The difference between the actual carbon number and measured ECN ranged from -24% to -2%. The difference between theoretical ECN and measured ECN ranged from -22% to 9%. Measured ECN values were within 10% of theoretical ECN values for most terpenoid compounds.

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

    Energy Technology Data Exchange (ETDEWEB)

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

    2015-06-15

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

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

    International Nuclear Information System (INIS)

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

  16. Reinforcing of thermoplastic polycarbonate and polysulfone with carbon fibers: Production and characteristics of UD-compound objects

    Science.gov (United States)

    Fitzer, E.; Jaeger, H.

    1988-01-01

    The production and characteristics of the carbon fiber reinforced thermoplastics polycarbonate and polysulfone are described. The production of prepregs from defined polymer solutions is emphasized along with methods of optimizing the production of compounds. The characteristics of unidirectionally reinforced thermoplastics, such as shear strength, bending strength, and impact resistance are compared with regard to fracture behavior, the influence of intermediate layers, and the behavior under cryogenic conditions and under slightly elevated temperatures. The problem of adhesion between high strength carbon fibers and thermoplastics is examined, taking into account the effect of moisture on the shear strength and the impact resistance.

  17. Carbon sources in the Beaufort Sea revealed by molecular lipid biomarkers and compound specific isotope analysis

    Directory of Open Access Journals (Sweden)

    I. Tolosa

    2012-10-01

    Full Text Available Molecular lipid biomarkers (hydrocarbons, alcohols, sterols and fatty acids and compound specific isotope analysis of suspended particulate organic matter (SPM and surface sediments of the Mackenzie Shelf and slope (Southeast Beaufort Sea, Arctic Ocean, were studied in summer 2009. The concentrations of the molecular lipid markers, characteristic of known organic matter sources, were grouped and used as proxies to evaluate the relative importance of fresh algal, detrital algal, fossil, C3 terrestrial plants, bacterial and zooplankton material in the sedimentary organic matter (OM.

    Fossil and detrital algal contributions were the major fractions of the freshwater SPM from the Mackenzie River with ~34% each of the total molecular biomarkers. Fresh algal, C3 terrestrial, bacterial and zooplanktonic components represented much lower percentages, 17, 10, 4 and < 1%, respectively. In marine SPM from the Mackenzie slope, the major contributions were fresh and detrital algal components (> 80% with a minor contribution of fossil and C3 terrestrial biomarkers. Characterization of the sediments revealed a major sink of refractory algal material mixed with some fresh algal material, fossil hydrocarbons and a small input of C3 terrestrial sources. In particular, the sediments from the shelf and at the mouth of the Amundsen Gulf presented the highest contribution of detrital algal material (60–75% whereas those from the slope contained the highest proportion of fossil (40% and C3 terrestrial plant material (10%. Overall, considering that the detrital algal material is marine derived, autochthonous sources contributed more than allochthonous sources to the OM lipid pool. Using the ratio of an allochthonous biomarker (normalized to total organic carbon, TOC found in the sediments to those measured at the river mouth water, we estimated that the fraction of terrestrial material preserved in the

  18. Synthesis and reactivity of compounds containing ruthenium-carbon, -nitrogen, and -oxygen bonds

    Energy Technology Data Exchange (ETDEWEB)

    Hartwig, J.F.

    1990-12-01

    The products and mechanisms of the thermal reactions of several complexes of the general structure (PMe{sub 3}){sub 4}Ru(X)(Y) and (DMPM){sub 2}Ru(X)(Y) where X and Y are hydride, aryl, and benzyl groups, have been investigated. The mechanism of decomposition depends critically on the structure of the complex and the medium in which the thermolysis is carried out. The alkyl hydride complexes are do not react with alkane solvent, but undergo C-H activation processes with aromatic solvents by several different mechanisms. Thermolysis of (PMe{sub 3}){sub 4}Ru(Ph)(Me) or (PMe{sub 3}){sub 4}Ru(Ph){sub 2} leads to the ruthenium benzyne complex (PMe{sub 3}){sub 4}Ru({eta}{sup 2}-C{sub 6}H{sub 4}) (1) by a mechanism which involves reversible dissociation of phosphine. In many ways its chemistry is analogous to that of early rather than late organo transition metal complexes. The synthesis, structure, variable temperature NMR spectroscopy and reactivity of ruthenium complexes containing aryloxide or arylamide ligands are reported. These complexes undergo cleavage of a P-C bond in coordinated trimethylphosphine, insertion of CO and CO{sub 2} and hydrogenolysis. Mechanistic studies on these reactions are described. The generation of a series of reactive ruthenium complexes of the general formula (PMe{sub 3}){sub 4}Ru(R)(enolate) is reported. Most of these enolates have been shown to bind to the ruthenium center through the oxygen atom. Two of the enolate complexes 8 and 9 exist in equilibrium between the O- and C-bound forms. The reactions of these compounds are reported, including reactions to form oxygen-containing metallacycles. The structure and reactivity of these ruthenium metallacycles is reported, including their thermal chemistry and reactivity toward protic acids, electrophiles, carbon monoxide, hydrogen and trimethylsilane. 243 refs., 10 tabs.

  19. Tracing carbon flow through coral reef food webs using a compound-specific stable isotope approach

    KAUST Repository

    McMahon, Kelton

    2015-11-21

    Coral reefs support spectacularly productive and diverse communities in tropical and sub-tropical waters throughout the world’s oceans. Debate continues, however, on the degree to which reef biomass is supported by new water column production, benthic primary production, and recycled detrital carbon (C). We coupled compound-specific stable C isotope ratio (δ13C) analyses with Bayesian mixing models to quantify C flow from primary producers to coral reef fishes across multiple feeding guilds and trophic positions in the Red Sea. Analyses of reef fishes with putative diets composed primarily of zooplankton (Amblyglyphidodon indicus), benthic macroalgae (Stegastes nigricans), reef-associated detritus (Ctenochaetus striatus), and coral tissue (Chaetodon trifascialis) confirmed that δ13C values of essential amino acids from all baseline C sources were both isotopically diagnostic and accurately recorded in consumer tissues. While all four source end-members contributed to the production of coral reef fishes in our study, a single-source end-member often dominated dietary C assimilation of a given species, even for highly mobile, generalist top predators. Microbially reworked detritus was an important secondary C source for most species. Seascape configuration played an important role in structuring resource utilization patterns. For instance, Lutjanus ehrenbergii showed a significant shift from a benthic macroalgal food web on shelf reefs (71 ± 13 % of dietary C) to a phytoplankton-based food web (72 ± 11 %) on oceanic reefs. Our work provides insights into the roles that diverse C sources play in the structure and function of coral reef ecosystems and illustrates a powerful fingerprinting method to develop and test nutritional frameworks for understanding resource utilization.

  20. Synthesis and reactivity of compounds containing ruthenium-carbon, -nitrogen, and -oxygen bonds

    International Nuclear Information System (INIS)

    The products and mechanisms of the thermal reactions of several complexes of the general structure (PMe3)4Ru(X)(Y) and (DMPM)2Ru(X)(Y) where X and Y are hydride, aryl, and benzyl groups, have been investigated. The mechanism of decomposition depends critically on the structure of the complex and the medium in which the thermolysis is carried out. The alkyl hydride complexes are do not react with alkane solvent, but undergo C-H activation processes with aromatic solvents by several different mechanisms. Thermolysis of (PMe3)4Ru(Ph)(Me) or (PMe3)4Ru(Ph)2 leads to the ruthenium benzyne complex (PMe3)4Ru(η2-C6H4) (1) by a mechanism which involves reversible dissociation of phosphine. In many ways its chemistry is analogous to that of early rather than late organo transition metal complexes. The synthesis, structure, variable temperature NMR spectroscopy and reactivity of ruthenium complexes containing aryloxide or arylamide ligands are reported. These complexes undergo cleavage of a P-C bond in coordinated trimethylphosphine, insertion of CO and CO2 and hydrogenolysis. Mechanistic studies on these reactions are described. The generation of a series of reactive ruthenium complexes of the general formula (PMe3)4Ru(R)(enolate) is reported. Most of these enolates have been shown to bind to the ruthenium center through the oxygen atom. Two of the enolate complexes 8 and 9 exist in equilibrium between the O- and C-bound forms. The reactions of these compounds are reported, including reactions to form oxygen-containing metallacycles. The structure and reactivity of these ruthenium metallacycles is reported, including their thermal chemistry and reactivity toward protic acids, electrophiles, carbon monoxide, hydrogen and trimethylsilane. 243 refs., 10 tabs

  1. A study of melt-compounded nanocomposites of polycarbonate and carbon nanotubes in the melt and solid states

    OpenAIRE

    Choong, Gabriel Y. H.

    2014-01-01

    Polycarbonate-carbon nanotube nanocomposites are promising materials for electrostatic shielding and conductive packaging applications. The nanotubes impart electrical conductivity and increases thermal conductivity and stiffness of the matrix. However, the nanofiller also affects the rheology, and hence the evolution of a filler network during processing. This thesis examines the effects of matrix molar mass and of compounding temperature on the thermal, rheological, electrical and mechanica...

  2. Tracing carbon fixation in phytoplankton—compound specific and total 13C incorporation rates

    OpenAIRE

    Grosse, J; van Breugel, P; Boschker, H.T.S.

    2015-01-01

    Measurement of total primary production using 13C incorporation is a widely established tool. However, these bulk measurements lack information about the fate of fixed carbon: the production of major cellular compounds (carbohydrates, amino acids, fatty acids, and DNA/RNA) is affected by for instance nutrient availability as their C:N:P requirements differ. Here, we describe an approach to combine established methods in gas chromatography/isotope ratio mass spectrometry (GC/C-IRMS) and recent...

  3. Preparing poly(aryl ethers) using alkaline earth metal carbonates, organic acid salts, and optionally copper compounds, as catalysts

    International Nuclear Information System (INIS)

    This patent describes an improved process for preparing poly(aryl ethers) and poly(aryl ether ketones) by the reaction of a mixture of at least one bisphenol and at least one dihalobenzenoid compound, and/or a halophenol. The improvement comprises providing to the reaction, a base which is a combination of an alkaline earth metal carbonate and/or bicarbonate and a potassium, rubidium, or cesium salt of an organic acid or combination of organic salts thereof

  4. Preparing poly(aryl ethers) using alkaline earth metal carbonates, organic acid salts, and optionally copper compounds, as catalysts

    Energy Technology Data Exchange (ETDEWEB)

    Winslow, P.A.; Kelsey, D.R.; Matzner, M.

    1988-09-27

    This patent describes an improved process for preparing poly(aryl ethers) and poly(aryl ether ketones) by the reaction of a mixture of at least one bisphenol and at least one dihalobenzenoid compound, and/or a halophenol. The improvement comprises providing to the reaction, a base which is a combination of an alkaline earth metal carbonate and/or bicarbonate and a potassium, rubidium, or cesium salt of an organic acid or combination of organic salts thereof.

  5. Effect of aromatics on the adsorption of thiophenic sulfur compounds from model diesel fuel by activated carbon cloth

    OpenAIRE

    NAVIRI FALLAH, Rahimeh; Azizian, Saeid; REGGERS, Guy; Carleer, Robert; Schreurs, Sonja; Ahenach, Janat; Meynen, Vera; Yperman, Jan

    2014-01-01

    The effects of aromatic compound presence in real diesel fuel on the adsorption of sulfur species onto activated carbon cloth (ACC) were investigated. Equilibrium and kinetics adsorption of benzothiophene (BT), dibenzothiophene (DBT) and 4,6-dimethyldibenzothiophene (DMDBT) in the presence of naphthalene (NP) and 1-methylnaphthalene (1-MNP) from prepared model diesel fuels onto ACC and its oxidized forms were studied. The total sulfur concentration inmodel diesel fuelwas 300 ppmw. The initial...

  6. Adsorptive removal of hydrophobic organic compounds by carbonaceous adsorbents: A comparative study of waste-polymer-based,coal-based activated carbon, and carbon nanotubes

    Institute of Scientific and Technical Information of China (English)

    Fei Lian; Chun Chang; Yang Du; Lingyan Zhu; Baoshan Xing; Chang Liu

    2012-01-01

    Adsorption of the hydrophobic organic compounds (HOCs) trichloroethylene (TCE),1,3-dichlorobenzene (DCB),1,3-dinitrobenzene (DNB) and γ-hexachlorocyclohexane (HCH) on five different carbonaceous materials was compared.The adsorbents included three polymer-based activated carbons,one coal-based activated carbon (F400) and multiwalled carbon nanotubes (MWNT).The polymerbased activated carbons were prepared using KOH activation from waste polymers:polyvinyl chloride (PVC),polyethyleneterephthalate (PET) and tire rubber (TR).Compared with F400 and MWNT,activated carbons derived from PVC and PET exhibited fast adsorption kinetics and high adsorption capacity toward the HOCs,attributed to their extremely large hydrophobic surface area (2700 m2/g) and highly mesoporous structures.Adsorption of small-sized TCE was stronger on the tire-rubber-based carbon and F400 resulting from the pore-filling effect.In contrast,due to the molecular sieving effect,their adsorption on HCH was lower.MWNT exhibited the lowest adsorption capacity toward HOCs because of its low surface area and characteristic of aggregating in aqueous solution.

  7. Application of mesoporous carbon as a solid-phase microextraction fiber coating for the extraction of volatile aromatic compounds.

    Science.gov (United States)

    Zhang, Xi; Zang, Xiaohuan; Zhang, Guijiang; Wang, Chun; Wang, Zhi

    2015-08-01

    A mesoporous carbon was fabricated using MCM-41 as a template and sucrose as a carbon source. The carbon material was coated on stainless-steel wires by using the sol-gel technique. The prepared solid-phase microextraction fiber was used for the extraction of five volatile aromatic compounds (chlorobenzene, ethylbenzene, o-xylene, bromobenzene, and 4-chlorotoluene) from tea beverage samples (red tea and green tea) prior to gas chromatography with mass spectrometric detection. The main experimental parameters affecting the extraction of the volatile aromatic compounds by the fiber, including the extraction time, sample volume, extraction temperature, salt addition, and desorption conditions, were investigated. The linearity was observed in the range from 0.1 to 10.0 μg/L with the correlation coefficients (r) ranging from 0.9923 to 0.9982 and the limits of detection were less than 10.0 ng/L. The recoveries of the volatile aromatic compounds by the method from tea beverage samples at spiking levels of 1.0 and 10.0 μg/L ranged from 73.1 to 99.1%. PMID:26041569

  8. Enhanced catalysis of the electrochemical hydrogen evolution reaction using composites of molybdenum-based compounds, gold nanoparticles and carbon.

    Science.gov (United States)

    Joshi, Ubisha; Lee, Jing; Giordano, Cristina; Malkhandi, Souradip; Yeo, Boon Siang

    2016-08-21

    Molybdenum nitride has been recently reported to interact synergistically with gold to show an enhanced activity for the electrochemical hydrogen evolution reaction (2H(+) + 2e(-)→ H2, HER). In this work, we elucidated the roles of nitrogen, carbon, molybdenum and gold on this observed phenomenon. Composites of Mo-based compounds, carbon black (black pearl 2000) and/or Au nanoparticles (AuNP) were prepared, and their activities for the HER in a 0.5 M H2SO4 electrolyte were measured using linear sweep voltammetry. We show and discuss here for the first time that, while the presence of carbon is necessary for the synergy phenomenon, the nitrogen atoms present in the compounds play no apparent role in this synergy. In fact, all the compounds containing Mo, namely Mo2N, MoB and metallic Mo(0), exhibited extensive synergy with Au for the HER. A hypothesis for the enhanced catalysis of H2 evolution by the mixed metal composites is proposed and discussed. PMID:27424516

  9. Compound-specific stable carbon isotope ratios of phenols and nitrophenols derivatized with N,O-bis(trimethylsilyl)trifluoroacetamide

    International Nuclear Information System (INIS)

    Graphical abstract: -- Highlights: •For GCC–IRMS analysis, an approach avoiding impact of NO2 on δ13C was demonstrated. •Carbon isotope fractionations during derivatizing reactions here were negligible. •Except some labile compounds, the overall bias of the method here was −0.21‰. •Even for the labile compounds, measurement biases ranged +1.2‰ to −1.4‰. •Real sample analysis demonstrates usefulness of the method for fractionation study. -- Abstract: We developed an analytical method for measuring compound-specific stable carbon isotope ratios (δ13C) of phenols and nitrophenols in filter samples of particulate organic matter. The method was tested on 13 phenols derivatized with N,O-bis(trimethylsilyl)trifluoroacetamide (BSTFA), together with four nonphenolic compounds. The data obtained by our method required two specific corrections for the determination of valid δ13C values: (1) for nitro compounds, the routine correction with use of m/z 46 for the contribution of 12C17O16O molecules) to m/z 45 was modified due to impact of NO2 on the m/z 46 trace, and (2) for the derivatized phenols, measured δ13C values were corrected for the shift in δ13C due to the addition of carbon atoms from the BSTFA moiety. Analysis of standard-spiked filters showed that overall there was a small compound-dependent bias in the δ13C values: the average bias ± the standard error of the mean of −0.21 ± 0.1‰ for the standard compounds tested, except 3-methylcatechol, methylhydroquinone, 4-methyl-2-nitrophenol, and 2,6-dimethyl-4-nitrophenol, whereas the average biases ± the standard errors of the mean for those were +1.2 ± 0.3‰, +1.2 ± 0.2‰, −1.2 ± 0.2‰, and −1.4 ± 0.5‰, respectively, when the injected mass of a derivatized compound exceeded 15 ngC. In situations where such small biases and uncertainties are acceptable, the method described here could be used to obtain valuable information about δ13C values. We also analyzed a real filter

  10. Secondary brown carbon - Formation of light-absorbing compounds in atmospheric particulates from selected dicarbonyls and amines

    Science.gov (United States)

    Kampf, Christopher; Filippi, Alexander; Hoffmann, Thorsten

    2015-04-01

    One of the main open questions regarding organic compounds in atmospheric chemistry today is related to the formation of optically-active compounds and the occurrence of so called brown carbon (Andreae and Gelencsér, 2006). While organic compounds in ambient fine particles for decades have been assumed to not absorb solar radiation, thus resulting in a net cooling effect on climate (IPCC, 2007), it is now generally accepted that a continuum of light-absorbing carbonaceous species is present in fine aerosols (Pöschl, 2003). In this study, light-absorbing compounds from reactions between dicarbonyl compounds, i.e., glyoxal, methylglyoxal, acetylacetone, 2,3-butanedione, 2,5-hexanedione, and glutaraldehyde, and amine species, i.e., ammonia and glycine, were investigated at atmospherically relevant concentrations in bulk solution experiments mimicking atmospheric particulates. Product analyses were performed using UV/Vis spectrophotometry and (ultra) high performance liquid chromatography coupled to diode array detection and ion trap mass spectrometry (HPLC-DAD-ESI-MS/MS), as well as ultra-high resolution (Orbitrap) mass spectrometry (UHPLC-ESI-HRMS/MS). We demonstrate that light-absorbing compounds are formed from a variety of atmospherically relevant dicarbonyls via particle phase reactions with amine nucleophiles. Single dicarbonyl and mixed dicarbonyl experiments were performed and products were analyzed. The reaction products are suggested to be cyclic nitrogen containing compounds such as imidazoles or dihydropyridines as well as open chain compounds resulting from aldol condensation reactions. Further, the reactive turnover was found to be higher at increasing pH values. The aforementioned processes may be of higher relevance in regions with high aerosol pH, e.g., resulting from high ammonia emissions as for example in northern India (Clarisse et al., 2009). References Andreae, M.O., and Gelencsér, A. (2006): Black carbon or brown carbon? The nature of light

  11. Detection of carbon-fluorine bonds in organofluorine compounds by Raman spectroscopy using a copper-vapor laser

    Science.gov (United States)

    Sharts, Clay M.; Gorelik, Vladimir S.; Agoltsov, A. M.; Zlobina, Ludmila I.; Sharts, Olga N.

    1999-02-01

    The Raman spectra of fluoro-organic compounds show specific emission bands for carbon-fluorine bonds in the range 500- 800 wave numbers (cm-1)). With very limited exceptions, biological materials do not contain carbon- fluorine bonds. Fluoro-organic compounds introduced into biological samples can be detected by a Raman emission signal. Normal mode C-F bond bands are observed: (1) at 710- 785 cm -1 for trifluoromethyl groups; (2) at 530-610 cm -1 for aromatic organofluorine bonds; (3) a range centered at 690 cm -1 for difluoromethylene groups. Specific examples of normal mode C-F bond emissions for organofluorine compounds containing trifluoromethyl groups are: 1-bromoperfluorooctane, 726 cm -1; perfluorodecanoic acid, 730 cm -1; triperfluoropropylamine, 750 cm -1; 1,3,5-tris- (trifluoromethyl)-benzene, 730 cm -1; Fluoxetine (Prozac) commercial powdered pill at 782 cm -1. Compounds containing aromatic C-F bonds are: hexafluorobenzene, 569 cm MIN1; pentafluoropyridine, 589 cm -1. Difluoromethylene groups: perfluorodecalin, 692 cm-1; perfluorocyclohexane, 691 cm -1. Raman spectra were observed with a standard single monochromator. The 510.8 nm light source was a copper-vapor laser operated at 3-10 watts with 10-12 nanosecond pulses at 10 kHz repetition rate. Detection was made with a time-gated photomultiplier tube. Resonance Raman spectra were also observed at 255.4 nm, using a frequency doubling crystal. Observed spectra were free of fluorescence with very sharp strong C-F lines.

  12. Effects of carbon black distribution on the electrical properties of Br/Epdm compounds

    International Nuclear Information System (INIS)

    The correlations between mechanical and electrical properties of butadiene/ethylene propylene diene terpolymer (BR/EPDM) and the distribution of carbon black levels are studied. It was found that the BR phase in the blends, compared to the EPDM phase, is more preferential for the used type of carbon black, probably because the lower viscosity and lower polarity of the BR phase. Tensile strength increases with an increase of carbon black. Possible reasons for these results are discussed

  13. Treatment of sludge containing nitro-aromatic compounds in reed-bed mesocosms – Water, BOD, carbon and nutrient removal

    International Nuclear Information System (INIS)

    Highlights: ► It is necessary to improve existing and develop new sludge management techniques. ► One method is dewatering and biodegradation of compounds in constructed wetlands. ► The result showed high reduction of all tested parameters after treatment. ► Plants improve degradation and Phragmites australis is tolerant to xenobiotics. ► The amount of sludge could be reduced by 50–70%. - Abstract: Since the mid-1970s, Sweden has been depositing 1 million ton d.w sludge/year, produced at waste water treatment plants. Due to recent legislation this practice is no longer a viable method of waste management. It is necessary to improve existing and develop new sludge management techniques and one promising alternative is the dewatering and treatment of sludge in constructed wetlands. The aim of this study was to follow reduction of organic carbon, BOD and nutrients in an industrial sludge containing nitro-aromatic compounds passing through constructed small-scale wetlands, and to investigate any toxic effect such as growth inhibition of the common reed Phragmites australis. The result showed high reduction of all tested parameters in all the outgoing water samples, which shows that constructed wetlands are suitable for carbon and nutrient removal. The results also showed that P. australis is tolerant to xenobiotics and did not appear to be affected by the toxic compounds in the sludge. The sludge residual on the top of the beds contained low levels of organic carbon and is considered non-organic and could therefore be landfilled. Using this type of secondary treatment method, the amount of sludge could be reduced by 50–70%, mainly by dewatering and biodegradation of organic compounds.

  14. Adsorption of organic compounds onto activated carbons from recycled vegetables biomass.

    Science.gov (United States)

    Mameli, Anna; Cincotti, Alberto; Lai, Nicola; Crisafulli, Carmelo; Sciré, Salvatore; Cao, Giacomo

    2004-01-01

    The removal of organic species from aqueous solution by activated carbons is investigated. The latter ones are prepared from olive husks and almond shells. A wide range of surface area values are obtained varying temperature and duration of both carbonization and activation steps. The adsorption isotherm of phenol, catechol and 2,6-dichlorophenol involving the activated carbons prepared are obtained at 25 degrees C. The corresponding behavior is quantitatively correlated using classical isotherm, whose parameters are estimated by fitting the equilibrium data. A two component isotherm (phenol/2,6-dichlorophenol) is determined in order to test activated carbon behavior during competitive adsorption. PMID:15347202

  15. Production and characterization of activated carbons from waste candeia (eremanthus erythropappus) and their application on organic compounds adsorption

    International Nuclear Information System (INIS)

    In this work, two activated carbons were prepared, using as activating agents ZnCl2 and K2CO3, denominated CA/ZnCl2,CA/ K2CO3, respectively, from waste generated in the process of extraction of essential oil of Candeia, a tree native of Brazil. These carbons were characterized by scanning electron microscopy, thermal analysis, elemental analysis, BET surface area and iodine index. These materials were tested in the adsorption of model molecules: Phenol and Methylene Blue, and a commercial activated carbon (Merck) was used for comparison purposes. Adsorption isotherms for CA/ZnCl2,CA/K2CO3 and CA/Com showed maximum sorption capacities of 297, 228 and 271 mg g-1 for Methylene Blue and 109,195 and 161 mg g-1 for phenol respectively. The results showed that the carbons are efficient in the adsorption process of molecules tested. The isotherms were fitted to equations of Langmuir and Freundlich. The Langmuir model provided better fit, showing that the adsorbents have energetically uniform surfaces. The materials produced were characterized as potential adsorbents for organic compounds that can be used as an alternative for obtaining activated carbons adding value to the residue.

  16. Monodisperse carbon nanopearls in a foam-like arrangement: a new carbon nano-compound for cold cathodes

    Energy Technology Data Exchange (ETDEWEB)

    Levesque, A.; Binh, Vu Thien; Semet, V.; Guillot, D.; Fillit, R.Y.; Brookes, M.D.; Nguyen, T.P

    2004-10-01

    This paper reports the low cost, high yield chemical vapor deposition synthesis of a potentially novel carbon nanomaterial using nickel nanocluster-catalysed dissociation of acetylene at 700 deg. C. The resulting 'carbon nanopearls' are 150 nm in diameter with {approx}85% monodispersity, with a solid structure composed of both amorphous and nanocrystalline ({approx}2 nm repeat unit) regions. The nanopearls form 3D space-filling 'strings' which give rise to a macroscopic foam-like appearance. The nanopearls have been characterized using scanning electron microscopy, high resolution transmission electron microscopy, X-ray microdiffraction, Raman spectroscopy and energy dispersive X-rays. A mechanism for the formation of the nanopearls is proposed based on concentric layers of {approx}4x4 nm graphitic flakes. The small radius of curvature of each nanopearl and the corrugation at the atomic scale of the surface resulting from the unclosed graphitic flakes result in excellent field emission properties. It has been demonstrated that a film of conditioned carbon nanopearls exhibits Fowler-Nordheim field emission behavior, with currents of up to 50 {mu}A readily obtainable under continuous emission in moderate vacuum. It is proposed that such emitters would provide significantly higher yield, uniform emission characteristics than non-oriented films of carbon nanotubes due to the reproducibly high density of nanopearl emitter sites.

  17. Optimizing sample pretreatment for compound-specific stable carbon isotopic analysis of amino sugars in marine sediment

    Science.gov (United States)

    Zhu, R.; Lin, Y.-S.; Lipp, J. S.; Meador, T. B.; Hinrichs, K.-U.

    2014-09-01

    Amino sugars are quantitatively significant constituents of soil and marine sediment, but their sources and turnover in environmental samples remain poorly understood. The stable carbon isotopic composition of amino sugars can provide information on the lifestyles of their source organisms and can be monitored during incubations with labeled substrates to estimate the turnover rates of microbial populations. However, until now, such investigation has been carried out only with soil samples, partly because of the much lower abundance of amino sugars in marine environments. We therefore optimized a procedure for compound-specific isotopic analysis of amino sugars in marine sediment, employing gas chromatography-isotope ratio mass spectrometry. The whole procedure consisted of hydrolysis, neutralization, enrichment, and derivatization of amino sugars. Except for the derivatization step, the protocol introduced negligible isotopic fractionation, and the minimum requirement of amino sugar for isotopic analysis was 20 ng, i.e., equivalent to ~8 ng of amino sugar carbon. Compound-specific stable carbon isotopic analysis of amino sugars obtained from marine sediment extracts indicated that glucosamine and galactosamine were mainly derived from organic detritus, whereas muramic acid showed isotopic imprints from indigenous bacterial activities. The δ13C analysis of amino sugars provides a valuable addition to the biomarker-based characterization of microbial metabolism in the deep marine biosphere, which so far has been lipid oriented and biased towards the detection of archaeal signals.

  18. Compound Hertzian Chain Model for Copper-Carbon Nanocomposites' Absorption Spectrum

    CERN Document Server

    Kokabi, Alireza; Saeedi, Saman; Moftakharzadeh, Ali; Vesaghi, Mohammad Ali; Fardmanesh, Mehdi

    2011-01-01

    The infrared range optical absorption mechanism of Carbon-Copper composite thin layer coated on the Diamond-Like Carbon (DLC) buffer layer has been investigated. By consideration of weak interactions between copper nanoparticles in their network, optical absorption is modeled using their coherent dipole behavior induced by the electromagnetic radiation. The copper nanoparticles in the bulk of carbon are assumed as a chain of plasmonic dipoles, which have coupling resonance. Considering nearest neighbor interactions for this metallic nanoparticles, surface plasmon resonance frequency ({\\omega}\

  19. Emissions to air in Sweden: carbon dioxide, methane, nitrous oxide, nitrogen oxides, carbon monoxide, volatile organic compounds and sulphur dioxide 1990-2000

    International Nuclear Information System (INIS)

    Greenhouse gases - Carbon dioxide from combustion and motor fuels, Methane and Laughing gas from agriculture Carbon dioxide (CO2) emissions in Sweden amounted to 56 million tonnes in 2000, which is minor decrease since 1990. Combustion of fossil fuels and the use of fuels in vehicles are the major sources of CO2 emissions. Methane is the second most important greenhouse gas, and it is emitted when bacteria degrade organic matter. In Sweden the main source is enteric fermentation from cattle. The emissions of methane were 324 000 tonnes 1990. In 2000 the emissions amounted to 280 000 tonnes, or a 14 per cent decrease. The third greenhouse gas, N2O is mostly emitted from agriculture. N2O emissions have fallen somewhat. Total emissions of sulphur dioxide (SO2) and nitrogen oxides (NOx, counted as NO2) in Sweden were 58,000 and 247,000 tonnes respectively in 2000. International air and maritime traffic is not included. The major source of SO2 emissions is combustion of fossil fuels. Road traffic is the major source of NOX emissions. Emissions of carbon monoxide (CO) and non-methane volatile organic compounds (NMVOCs) are also presented in this report. The main source of CO is road traffic, while NMVOCs come from household combustion and road traffic. Emission trends for fluoride carbon greenhouse gases HFCs, PFCs and SF6 are also presented. These gases mainly emit from refrigerators, freezing and air conditioning equipment (e.g. in cars and buildings) and from heat pumps

  20. Wax ester-like compounds as biosurfactants produced by Dietzia maris from n-alkane as a sole carbon source.

    Science.gov (United States)

    Nakano, Miyo; Kihara, Masaki; Iehata, Shunpei; Tanaka, Reiji; Maeda, Hiroto; Yoshikawa, Takeshi

    2011-10-01

    The hydrocarbon-degrading bacterium Dietzia maris WR-3 was isolated from a consortium comprising ammonia-oxidizing and denitrifying bacteria derived from marine sediments. Here, we examined biosurfactant production by strain WR-3 when cultured using several different carbon (D-glucose, n -decane, n -hexadecane, motor oil, olive oil, and rapeseed oil) and nitrogen (NH(4) )(2) SO(4) , NaNO(3) , yeast extract, and polypeptone) sources as growth substrates. Strain WR-3 was able to grow and reduce the surface tension of culture broth to 31±1.0 mN m(-1) when cultured using n -hexadecane and nitrate ions. The surface-active compounds produced by strain WR-3 were extracted and analyzed by thin layer chromatography. Moreover, the main components in the extract were further purified and subjected to gas chromatography/mass spectrometry (GC/MS). From the analysis, the surface-active compounds were tentatively identified as wax ester-like compounds, which were synthesized from the degradation process of n -alkane. The production of surface-active compounds by strain WR-3 promoted attachment of cells to hydrocarbon droplets via increased cell hydrophobicity, thus allowing enhanced degradation of water immiscible substrates. As Dietzia spp. can grow and produce wax esters from the degradation process of hydrocarbons, these marine bacteria are potentially useful for the bioremediation of hydrocarbon-contaminated environments. PMID:21656811

  1. Product and corporate carbon footprint using the compound method based on financial accounts. The case of Osorio wind farms

    International Nuclear Information System (INIS)

    Highlights: • We applied novel organisation-product-based-life-cycle assessment to Osorio Wind Farms. • This study includes sources, phases and areas previously unreported for the wind power sector. • MC3 assess carbon footprint in a practical and comprehensive manner. • MC3 is suitable for its application in major international projects. - Abstract: The challenge of developing clean and renewable energy sources is becoming ever more urgent. Over the last decade, the concept of carbon footprint has been used to report direct and indirect greenhouse gas emissions and as a support for sustainable consumption decisions. However, the discrepancies in the approaches based on either the product or corporate carbon footprint can seriously hinder its successful implementation. The so-called compound method based on financial accounts is a tiered hybrid method which enables the calculation of both the product and corporate carbon footprint. This work aims to assess this method as a tool for carbon footprint through its implementation in a comprehensive life-cycle assessment of the Osorio Wind Farms in Brazil. The total cumulative life-cycle emissions are 362.455 t CO2eq, representing 18.33 gr CO2eq per kW h delivered to the Brazilian national power grid. The difference with regard to previous works derives from its broader scope and different assumptions. In this study the comparable value from wind turbine manufacture, transport and construction is 8.42 gr CO2eq per kW h, 56% lower than the mean figure reported by Arvesen and Hertwich (2012). This study includes sources, phases and areas previously unreported in the carbon footprint reviews for the wind power sector. We conclude that the compound method based on financial accounts is a practical method that allows the definition of a more comprehensive goal and scope. Its implementation at Osorio Wind Farms demonstrates the method’s suitability for application in major international projects and institutions

  2. Control of atmospheric emissions of volatile organic compounds using impregnated active carbons

    Energy Technology Data Exchange (ETDEWEB)

    Alvim Ferraz, M.C.M.; Moeser, S.; Tonhaeeuser, M. [Oporto University, Oporto (Portugal). Chemical Engineering Dept.

    1999-10-01

    The combination of carbon adsorption with catalytic complete oxidation for control of emissions of n-hexane, 2,3-dimethylbutane, cyclohexane and benzene is analysed. The activities of activated carbons prepared with almond shells and impregnated with CoO, Co{sub 3}O{sub 4} and CrO{sub 3} were compared, in relation with carbon structure, catalyst content and catalyst species. The microcatalytic-chromatographic technique developed was very suitable for rapid comparison of catalytic activities, that are higher for carbons with a better development of surface area and pore volumes, and increased with increasing catalyst content. Catalytic activity of cobalt is better than that of chromium, the oxidation state of cobalt in Co{sub 3}O{sub 4} being better than in CoO. The catalytic activity depends clearly on the hydrocarbons chemical structure. 20 refs., 4 figs., 3 tabs.

  3. Mass spectrometric analysis of stable carbon isotopes in abiogenic and biogenic natural compounds

    International Nuclear Information System (INIS)

    This report describes the general methodology of sup/13/ carbon analysis on mass spectrometer and various preparation systems developed for conversion of samples into isotopically non-fractionated and purified carbon dioxide. Laboratory standards required for sup/13/ C analysis have been calibrated against international standards. The reproducibility/accuracy of sample preparation and analysis on mass spectrometer for sup/13/ C or sup/12/ C measurement is well within the internationally acceptable limits. (author)

  4. Applicability of Activated Carbon to Treatment of Waste Containing Iodine-Labeled Compounds

    International Nuclear Information System (INIS)

    The applicability of activated carbon prepared from sawdust (SD) by one-step chemical activation process using H3PO4 (H) to treatment of aqueous waste contaminated with iodine-labeled prolactin (I-PRL) has been investigated. Treatment processes were performed under the varying conditions; contact time, temperature, carbon type, carbon dosage, and different particle size of activated carbon (SDH). Effect of aqueous waste volume has been investigated to calculate the batch factor (V/M) and the distribution coefficient (Kd). The used activated carbon (SDH) was characterized by N2 adsorption, FTIR, density, ph, point of zero charge phpzc, moisture and ash content. Methylene blue (MB) and iodine number was calculated by adsorption from solution. In order to investigate the mechanism of sorption and potential rate controlling steps, pseudo first- and second-order equations, intra particle diffusion equation and the Elovich equation have been used to test experimental data. Kinetic analysis of the four models has been carried out for system variables in order to assess which model provides the best fit predicted data with experimental results. 7 M NaOH can be used for regeneration of spent SDH activated carbon with the efficiency of 99.6% and the regenerated carbon can be reused for five cycles effectively. The prospect of applying the SDH activated carbon prepared from agricultural by-product, sawdust, to treatment of aqueous waste contaminated with I-PRL appears promising and is considered highly applicable because of its high adsorption capacity, available at low cost, easily regenerated and reused

  5. Modeling the heat and mass transfers in temperature-swing adsorption of volatile organic compounds onto activated carbons

    Energy Technology Data Exchange (ETDEWEB)

    Sylvain Giraudet; Pascaline Pre; Pierre Le Cloirec [Ecole des Mines de Nantes, Nantes (France)

    2009-02-15

    A theoretical model was built to simulate the adsorption of volatile organic compounds (VOCs) onto activated carbons in a fixed bed. This model was validated on a set of experimental data obtained for the adsorption of acetone, ethyl formate, and dichloromethane onto five commercial activated carbons. The influence of operating conditions was modeled with various VOC contents at the inlet of the adsorber and superficial velocities of the gas-phase from 0.14 to 0.28 m.s{sup -1}. Breakthrough times and maximum temperature rises were computed with a coefficient of determination of 0.988 and 0.901, respectively. The simulation was then extended to the adsorption of mixtures of VOCs. From the comparison of simulation and experimental results, the advantage of accounting for dispersions of heat and mass is shown and the importance in taking into account the temperature effect on the equilibrium data is demonstrated. 29 refs., 6 figs., 1 tab.

  6. Carbon-13 magnetic relaxation rates or iron (III) complexes of some biogenic amines and parent compounds in aqueous solutions

    International Nuclear Information System (INIS)

    Spin-lattice relaxation rates (R1) from naturally occuring C-13 F.T. N.M.R. spectra of some catecholamines and parent compounds with Iron(III) at pD = 4 were determined in order to elucidate the molecular mechanism underlying their association in aqueous solutions. Complexation was observed only for catecholic ligands. The R1 values were used to calculate iron-carbon scaled distances, and two complexation models were proposed where the catecholic function binds Fe(III) in the first and second coordination spheres respectively. The latter case was shown to be the consistent with the molecular geometries. (orig.)

  7. Improvement in Superconducting Properties of MgB2 Superconductors by Nanoscale Carbon-Based Compound Doping

    Institute of Scientific and Technical Information of China (English)

    Si-Hai Zhou

    2008-01-01

    MgB2 is a relatively new superconductor; it has attracted great interest from superconductor researchers all over the world. Thorough investigations have been carried out to study the material fabrication, as well as to study the material and superconducting properties from a fundamental physics point of view. The University of Wollongong has played a very active role in this research and a leading role in the research on high critical current density and high critical magnetic fields. Our recent research on the improve- ment of critical current density and the upper critical magnetic field by carbon-based compound doping is reviewed in this paper.

  8. Compound-specific carbon isotopic fractionation during transport of phthalate esters in sandy aquifer.

    Science.gov (United States)

    Liu, Hui; Li, YanXi; He, Xi; Sissou, Zakari; Tong, Lei; Yarnes, Chris; Huang, Xianyu

    2016-02-01

    The present paper aims to evaluate the carbon isotopic fractionation of phthalate esters (PAEs) during transport in an sandy aquifer. Breakthrough curves of di-methyl phthalate (DMP), di-ethyl phthalate (DEP), and di-n-butyl phthalate (DBP) in mixed solution were determined by miscible displacement experiment, and simulated using HYDRUS-1D software. The stable carbon isotopes (δ(13)C) of 3 PAEs in effluent were analyzed at different times. Results showed that, in the transport process in sandy sediment, PAEs are mainly trapped into the pore space instead of being adsorbed on the surface of particles. At the initial stage of transport, PAEs with lighter carbon tend to run faster in the sandy sediment, and PAEs with heavier carbon run after. However, there is no priority for the transport of PAEs with different carbon isotopes at Stage Ⅱ with mainly time-limited sorption. So the transport-based isotope fractionation occurs in the front area of contaminant plume. This effect may be relevant for interpreting carbon isotope signatures in the real contaminant site. PMID:26539707

  9. A semi-micro combustion assembly for the determination of carbon and hydrogen in actinide compounds

    International Nuclear Information System (INIS)

    A rapid combustion unit (Baird and Tatlock) incorporating a combustion chamber provided with baffle plates for complete combustion of the sample without the use of a catalyst has been assembled in a glove box for the determination of carbon and hydrogen in actinide complexes. The unit has been modified employing a movable electric furnace and a proportional temperature controller, for decomposition of the sample at desired heating rates. The set-up was standardised employing various reference materials such as benzoic acid, acetanilide, sulphanilamide and 1-chloro 2:4 dinitrobenzene and the standard deviation in the measurements evaluated. It has also been used successfully for the determination of carbon in uranium carbide and carbon and hydrogen in some uranyl-β-diketone-amine N-oxide complexes and in plutonium(IV) oxalate. (auth.)

  10. Magnetic resonance and optical study of carbonized silica obtained bypyrolysis of surface compounds

    Czech Academy of Sciences Publication Activity Database

    Savchenko, Dariia; Kalabukhova, E.; Sitnikov, A.; Vasin, A.V.; Starik, S.; Gontar, O.; Rudko, G.; Nazarov, A.N.; Lysenko, V.S.; Tertykh, V.

    Zurich: Trans Tech Publications, 2014 - (Nazarov, A.; Lysenko, V.; Flandre, D.), s. 99-104. (Advanced Materials Research. 854). ISBN 9783037859421. ISSN 1022-6680. [International Workshop on Functional Nanomaterials and Devices /7./. Kyiv (UA), 08.04.2013-11.04.2013] R&D Projects: GA MŠk(CZ) LM2011029 Grant ostatní: SAFMAT(XE) CZ.2.16/3.1.00/22132 Institutional support: RVO:68378271 Keywords : carbonized silica nanopowders * annealing * EPR * carbon radicals * PL * IR absorption Subject RIV: BM - Solid Matter Physics ; Magnetism

  11. Source characterization using compound composition and stable carbon isotope ratio of PAHs in sediments from lakes, harbor, and shipping waterway

    International Nuclear Information System (INIS)

    Molecular compositions and compound specific stable carbon isotope ratios of polycyclic aromatic hydrocarbons (PAH) isolated from sediments were used to characterize possible sources of contamination at an urban lake, a harbor, a shipping waterway, and a relatively undisturbed remote lake in the northwest United States. Total PAH concentrations in urban lake sediments ranged from 66.0 to 16,500 μg g-1 dry wt. with an average of 2600 μg g-1, which is ∼ 50, 100, and 400 times higher on average than PAH in harbor (48 μg g-1 on average), shipping waterway (26 μg g-1), and remote lake (7 μg g-1) sediments, respectively. The PAH distribution patterns, methyl phenanthrene/phenanthrene ratios, and a pyrogenic index at the sites suggest a pyrogenic origin for PAHs. Source characterization using principal component analysis and various molecular indices including C2-dibenzothiophenes/C2-phenanthrenes, C3-dibenzothiophenes/C3-phenanthrenes, and C2-chrysenes/C2-phenanthrenes ratios, was able to differentiate PAH deposited in sediments from the four sites. The uniqueness of the source of the sediment PAHs from urban lake was also illustrated by compound specific stable carbon isotope analysis. It was concluded that urban lake sediments are accumulating PAH from sources that are unique from contamination detected at nearby sites in the same watershed

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

    Science.gov (United States)

    Nosbi, Norlin; Akil, Hazizan Md

    2015-06-01

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

  13. Comparison of Bulk and Compound-Specific Carbon Isotope Analyses and Determination of Carbon Sources to Salt Marsh Sediments Using n-Alkane Distributions (Maine, USA)

    Science.gov (United States)

    Tanner, B. R.; Uhle, M. E.; Kelley, J. T.; Mora, C. I.

    2005-12-01

    Sources of sedimentary organic matter to a Morse River, Maine (USA) salt marsh over the last 3390+/-60 RCYBP are determined using distribution patterns of n-alkanes as well as bulk and compound-specific carbon isotopic analysis. Marsh foraminiferal counts indicate the ubiquitous presence of zone 1B deposits, suggesting that the deposits were laid down ~0.2 to 0.5m above mean high water. Distributions of n-alkanes show a primary contribution from higher plants, confirmed by an average ACL value of 27.5 for the core sediments and CPI values above 3. Many sample depths have a maximum abundance at the C25 alkane. Ten low marsh, high marsh, and higher-high marsh plant species common to Maine salt marshes were sampled, including Spartina alterniflora, Spartina patens, Juncus gerardi and Solidago sempervirens. The ACL value for the average of the 10 marsh species is 29.1. Salicornia europa, usually not considered to be a dominant species in Maine marshes, has a similar n-alkane distribution to many of the salt marsh sediments, suggesting that it is an important source to the biomass of the marsh through time. Bacterial degradation or algal inputs to the marsh sediments appear to be minor. Compound specific carbon isotopic analyses of the C27 alkanes are, on average, 7.2ppt. depleted relative to bulk values, but the two records are strongly correlated (R2 = 0.87), suggesting that marsh plants are "swamping" the bulk carbon isotopic signal. The apparent abundance of a subordinate (though common) salt marsh plant species (Salicornia europa) within our core underscores the importance of using caution when applying mixing models of relatively few plant species to marsh sediments.

  14. A review of volatile compounds in tektites, and carbon content and isotopic composition of moldavite glass

    Czech Academy of Sciences Publication Activity Database

    Žák, Karel; Skála, Roman; Řanda, Zdeněk; Mizera, Jiří

    2012-01-01

    Roč. 47, č. 6 (2012), s. 1010-1028. ISSN 1086-9379 R&D Projects: GA ČR GA205/09/0991 Institutional research plan: CEZ:AV0Z30130516; CEZ:AV0Z10480505 Keywords : moldavites * geochemistry * ries * carbon stable isotopes * moldavites (Germany) Subject RIV: DD - Geochemistry Impact factor: 2.800, year: 2012

  15. Charcoal and activated carbon as adsorbate of phytotoxic compounds - a comparative study.

    NARCIS (Netherlands)

    Hille, M.G.; Ouden, den J.

    2005-01-01

    This study compares the potential of natural charcoal from Scots pine (Pinus sylvestris L.) and activated carbon to improve germination under the hypothesis that natural charcoal adsorbs phytotoxins produced by dwarf-shrubs, but due to it's chemical properties to a lesser extent than activated carbo

  16. The Path of Carbon in Photosynthesis XVII. Phosphorus Compounds as Intermediates in Photosynthesis

    Science.gov (United States)

    Buchanan, J. G.; Bassham, J. A.; Benson, A. A.; Bradley, D. F.; Calvin, M.; Daus, L. L.; Goodman, M.; Hayes, P. M.; Lynch, V. H.; Norris, L. T.; Wilson, A. T.

    1952-07-08

    Studies of carbon dioxide fixation in green plants using the C{sup 14} isotope have shown that in very short times phosphoglyceric acid contains most of the radioactivity. The tracer is present almost entirely in the carboxyl group. The importance of organic phosphates in the subsequent metabolism of phosphoglyceric acid can be seen from the accompanying photographs.

  17. Pulsed amperometric detection at glassy carbon electrodes: A new waveform for sensitive and reproducible determination of electroactive compounds.

    Science.gov (United States)

    Nardiello, Donatella; Palermo, Carmen; Natale, Anna; Quinto, Maurizio; Centonze, Diego

    2015-09-24

    In this work, the application of a new pulsed amperometric detection (PAD) waveform at a glassy carbon electrode, operating in typical chromatographic mobile phases, is proposed for the sensitive and reproducible determination of arylethanolaminic and phenolic moiety based compounds (e.g. beta-agonists and polyphenols). Preliminary experiments by cyclic voltammetry were carried out to investigate the electrochemical behaviour and to select the detection and cleaning electrode potentials. The proposed potential-time profile was designed to prevent the carbon electrode fouling under repeated analyses, thus ensuring a reproducible and sensitive quantitative determination, without the need of any mechanical or chemical electrode cleaning procedure. The waveform electrochemical parameters, including detection and delay times, were optimized in terms of sensitivity, limit of detection and response stability. The optimized waveform allowed the sensitive and stable detection of model compounds, such as clenbuterol and caffeic acid, that showed detection limits of 0.1 μg L(-1) and 14 μg L(-1), quantification limits of 0.4 μg L(-1) and 46 μg L(-1), and linearity up to 100 μg L(-1) (r = 0.9993) and 10 mg L(-1) (r = 0.9998), respectively. Similar results were obtained for other compounds of the same classes, with precision values under repeatability conditions ranging from 3.0 to 5.9%. The proposed method can be then considered as an excellent alternative to the post-column detection of beta-agonists, phenols and polyphenols. PMID:26423623

  18. Optimizing sample pretreatment for compound-specific stable carbon isotopic analysis of amino sugars in marine sediment

    Directory of Open Access Journals (Sweden)

    R. Zhu

    2014-01-01

    Full Text Available Amino sugars are quantitatively significant constituents of soil and marine sediment, but their sources and turnover in environmental samples remain poorly understood. The stable carbon isotopic composition of amino sugars can provide information on the lifestyles of their source organisms and can be monitored during incubations with labeled substrates to estimate the turnover rates of microbial populations. However, until now, such investigation has been carried out only with soil samples, partly because of the much lower abundance of amino sugars in marine environments. We therefore optimized a procedure for compound-specific isotopic analysis of amino sugars in marine sediment employing gas chromatography-isotope ratio mass spectrometry. The whole procedure consisted of hydrolysis, neutralization, enrichment, and derivatization of amino sugars. Except for the derivatization step, the protocol introduced negligible isotopic fractionation, and the minimum requirement of amino sugar for isotopic analysis was 20 ng, i.e. equivalent to ~ 8 ng of amino sugar carbon. Our results obtained from δ13C analysis of amino sugars in selected marine sediment samples showed that muramic acid had isotopic imprints from indigenous bacterial activities, whereas glucosamine and galactosamine were mainly derived from organic detritus. The analysis of stable carbon isotopic compositions of amino sugars opens a promising window for the investigation of microbial metabolisms in marine sediments and the deep marine biosphere.

  19. Isolation of Bioactive Compounds from Sunflower Leaves (Helianthus annuus L.) Extracted with Supercritical Carbon Dioxide.

    Science.gov (United States)

    El Marsni, Zouhir; Torres, Ascension; Varela, Rosa M; Molinillo, José M G; Casas, Lourdes; Mantell, Casimiro; Martinez de la Ossa, Enrique J; Macias, Francisco A

    2015-07-22

    The work described herein is a continuation of our initial studies on the supercritical fluid extraction (SFE) with CO2 of bioactive substances from Helianthus annuus L. var. Arianna. The selected SFE extract showed high activity in the wheat coleoptile bioassay, in Petri dish phytotoxicity bioassays, and in the hydroponic culture of tomato seeds. Chromatographic fractionations of the extracts and a spectroscopic analysis of the isolated compounds showed 52 substances belonging to 10 different chemical classes, which were mainly sesquiterpene lactones, diterpenes, and flavonoids. Heliannuol M (31), helivypolides K and L (36, 37), and helieudesmanolide B (38) are described for the first time in the literature. Metabolites have been tested in the etiolated wheat coleoptile bioassay with good results in a noteworthy effect on germination. The most active compounds were also tested on tomato seeds, heliannuol A (30) and leptocarpin (45) being the most active, with values similar to those of the commercial herbicide. PMID:26151222

  20. The stopping power and carbon ion ranges in elements and compounds

    International Nuclear Information System (INIS)

    Possibility of the heavy ions stopping cross sections calculation are discussed. The stopping ppower and C12 ions ranges are evaluated using the protons stopping data in matter and Pirson's and Blanns formula for the effectvive charge. The energy losses due to the elastic collisions with atoms have been taken into account in low energies. The RBregg's rule was used to calculate the stopping power of compounds. The comparison with the evailable data showed a good agreement. The C12 ions ranges with energies from 0.01 to 10 NMeV/nucleon for elements from hydrogen to uranium and several compounds are tabulated. The C12 ions energy losses in the layers of definite thickness can be determined using these tables

  1. Quantum efficiency of energy transfer in noncovalent carbon nanotube/porphyrin compounds

    OpenAIRE

    Roquelet, Cyrielle; Garrot, Damien; Lauret, Jean-Sébastien; Voisin, C.; Alain-Rizzo, Valérie; Roussignol, Philippe; Delaire, Jacques,; Deleporte, Emmanuelle

    2010-01-01

    We report on the quantum yield of excitation energy transfer in non-covalently bound nan- otube/porphyrin compounds. Evidence for energy transfer is gained from photoluminescence exci- tation experiments. We perform a quantitative evaluation of the transfer quantum yield in the case of (6,5) nanotubes through three independent methods : quantitative PLE measurements, evalu- ation of the luminescence quenching of the donor (porphyrin) and ultrafast transient absorption measurements. The latter...

  2. Effect of Functional Group and Carbon Chain Length on the Odor Detection Threshold of Aliphatic Compounds

    Directory of Open Access Journals (Sweden)

    Manuel Zarzo

    2012-03-01

    Full Text Available Odor detection thresholds (ODTs are used for assessing outdoor and indoor air quality. They are obtained experimentally by olfactometry and psychophysical methods, and large compilations are available in the literature. A non-linear regression equation was fitted to describe the ODT variability of 114 aliphatic compounds based on the alkyl chain length for different homologous series (carboxylic acids, aldehydes, 2-ketones, esters, 1-alcohols, amines, thiols, thioethers and hydrocarbons. The resulting equation reveals an effect of the functional group, molecular size and also an interaction between both factors. Although the mechanistic interpretation of results is uncertain, the relatively high goodness-of-fit (R2 = 0.90 suggests that ODT values of aliphatic compounds can be predicted rather accurately, which is not the case for rigid molecules. This equation may serve as a basis for the development of more complex ODT models taking into account diverse structural features of odorants. The variability of power-law exponents was also investigated for the homologous series.

  3. Emissions to air in Sweden: sulphur dioxide, nitrogen oxides, carbon dioxide, methane, nitrous oxide, carbon monoxide and volatile organic compounds, 1999

    International Nuclear Information System (INIS)

    The method for calculating emissions to air has been revised, which has led to adjustments. Because of this, emissions in 1999 cannot yet be compared with previous years. Emissions in 1990 - 1998 are being recalculated now using the new method and are expected to be ready during 2001. Emissions to air of carbon dioxide (CO2) in Sweden was 56.58 million tonnes in 1999, not including emissions from biofuels and international bunkers. The major sources of CO2 emissions are the combustion of fossil fuels and the use of fuels for mobile sources. Total emissions to air of sulphur dioxide (SO2) and nitrogen oxides (NOx, counted as NO2) in Sweden was 66 000 and 263 000 tonnes respectively in 1999. International bunkers are not included. The major source of SO2 emissions is combustion of fossil fuels. Road traffic is the major source of NOx emissions. Emissions to air of methane (CH4), nitrous oxide (N2O), carbon monoxide (CO) and volatile organic compounds (NMVOC) in 1999 were 253 000, 26 000, 924 000 and 430 000 tonnes respectively, not including international bunkers. Agriculture is the major source of CH4 and N2O emissions. CO mainly derives from road traffic and NMVOC mainly derives from household combustion and road traffic

  4. Unusual route for preparation of manganese(II), cobalt(II), zinc(II) and cadmium(II) carbonate compounds: synthesis and spectroscopic characterizations

    Indian Academy of Sciences (India)

    Moamen S Refat; Mohsen M Al-Qahtani

    2011-07-01

    The manganese(II) carbonate, MnCO3.H2O, cobalt(II) carbonate, CoCO3.4H2O, zinc(II) carbonate, ZnCO3 and cadmium(II) carbonate, CdCO3, respectively, were synthesis by a new simple unusual route during the reaction of aqueous solutions of MnX2, CoX2, ZnX2 and CdX2, where (X = Br- and ClO$^{-}_{4}$) with urea at high temperature within ∼ 90°C for 6 h. The infrared spectra of the reaction products clearly indicate the absence of the bands of urea, but show the characteristic bands of ionic carbonate, CO$^{2-}_{3}$. A general mechanism describing the preparation of manganese(II), cobalt(II), zinc(II) and cadmium(II) carbonate compounds are discussed.

  5. Photocatalytic and chemical oxidation of organic compounds in supercritical carbon dioxide. Progress report for FY97

    International Nuclear Information System (INIS)

    'The background for the project is briefly reviewed and the work done during the nine months since funding was received is documented. Work began in January, 1997. A post doctoral fellow joined the team in April. The major activities completed this fiscal year were: staffing the project, design of the experimental system, procurement of components, assembly of the system. preparation of the Safe Operating Procedure and ES and H compliance, pressure testing, establishing data collection and storage methodology, and catalyst preparation. Objective The objective of the project is to develop new chemistry for the removal of organic contaminants from supercritical carbon dioxide. This has application in processes used for continuous cleaning and extraction of parts and waste materials. A secondary objective is to increase the fundamental understanding of photocatalytic chemistry. Cleaning and extraction using supercritical carbon dioxide (scCO2) can be applied to the solution of a wide range of environmental and pollution prevention problems in the DOE complex. Work is being done that explores scCO2 in applications ranging from cleaning contaminated soil to cleaning components constructed from plutonium. The rationale for use of scCO2 are based on the benign nature, availability and low cost, attractive solvent properties, and energy efficient separation of the extracted solute from the solvent by moderate temperature or pressure changes. To date, R and D has focussed on the methods and applications of the extraction steps of the process. Little has been done that addresses methods to polish the scCO2 for recycle in the cleaning or extraction operations. In many applications it will be desirable to reduce the level of contamination from that which would occur at steady state operation of a process. This proposal addresses chemistry to achieve that. This would be an alternative to removing a fraction of the contaminated scCO2 for disposal and using makeup scCO2. A

  6. Efficient utilization of pentoses for bioproduction of the renewable two-carbon compounds ethylene glycol and glycolate.

    Science.gov (United States)

    Pereira, Brian; Li, Zheng-Jun; De Mey, Marjan; Lim, Chin Giaw; Zhang, Haoran; Hoeltgen, Claude; Stephanopoulos, Gregory

    2016-03-01

    The development of lignocellulose as a sustainable resource for the production of fuels and chemicals will rely on technology capable of converting the raw materials into useful compounds; some such transformations can be achieved by biological processes employing engineered microorganisms. Towards the goal of valorizing the hemicellulose fraction of lignocellulose, we designed and validated a set of pathways that enable efficient utilization of pentoses for the biosynthesis of notable two-carbon products. These pathways were incorporated into Escherichia coli, and engineered strains produced ethylene glycol from various pentoses, including simultaneously from D-xylose and L-arabinose; one strain achieved the greatest reported titer of ethylene glycol, 40g/L, from D-xylose at a yield of 0.35g/g. The strategy was then extended to another compound, glycolate. Using D-xylose as the substrate, an engineered strain produced 40g/L glycolate at a yield of 0.63g/g, which is the greatest reported yield to date. PMID:26711083

  7. Extraction of semivolatile organic compounds from high-efficiency particulate air (HEPA) filters by supercritical carbon dioxide

    International Nuclear Information System (INIS)

    Supercritical fluid extraction (SFE) using unmodified carbon dioxide has been explored as an alternative method for the extraction of semivolatile organic compounds from high-efficiency particulate air (HEPA) filters. HEPA filters provide the final stage of containment on many exhaust systems in US Department of Energy (DOE) facilities by preventing the escape of chemical and radioactive materials entrained in the exhausted air. The efficiency of the filters is tested by the manufacturer and DOE using dioctylphthalate (DOP), a substance regulated by the US Environmental Protection Agency under the Resource Conservation and Recovery Act. Therefore, the filters must be analyzed for semivolatile organics before disposal. Ninety-eight acid, base, and neutral semivolatile organics were spiked onto blank HEPA material and extracted using SFE, Soxhlet, automated Soxhlet, and sonication techniques. The SFE conditions were optimized using a Dionex SFE-703 instrument. Average recoveries for the 98 semivolatile compounds are 82.7% for Soxhlet, 74.0% for sonication, 70.2% for SFE, and 62.9% for Soxtec. Supercritical fluid extraction reduces the extraction solvent volume to 10--15 mL, a factor of 20--30 less than Soxhlet and more than 5 times less than Soxtec and sonication. Extraction times of 30--45 min are used compared to 16--18 h for Soxhlet extraction

  8. Compound-specific carbon and hydrogen isotope analysis of sub-parts per billion level waterborne petroleum hydrocarbons

    Science.gov (United States)

    Wang, Y.; Huang, Y.; Huckins, J.N.; Petty, J.D.

    2004-01-01

    Compound-specific carbon and hydrogen isotope analysis (CSCIA and CSHIA) has been increasingly used to study the source, transport, and bioremediation of organic contaminants such as petroleum hydrocarbons. In natural aquatic systems, dissolved contaminants represent the bioavailable fraction that generally is of the greatest toxicological significance. However, determining the isotopic ratios of waterborne hydrophobic contaminants in natural waters is very challenging because of their extremely low concentrations (often at sub-parts ber billion, or even lower). To acquire sufficient quantities of polycyclic aromatic hydrocarbons with 10 ng/L concentration for CSHIA, more than 1000 L of water must be extracted. Conventional liquid/liquid or solid-phase extraction is not suitable for such large volume extractions. We have developed a new approach that is capable of efficiently sampling sub-parts per billion level waterborne petroleum hydrocarbons for CSIA. We use semipermeable membrane devices (SPMDs) to accumulate hydrophobic contaminants from polluted waters and then recover the compounds in the laboratory for CSIA. In this study, we demonstrate, under a variety of experimental conditions (different concentrations, temperatures, and turbulence levels), that SPMD-associated processes do not induce C and H isotopic fractionations. The applicability of SPMD-CSIA technology to natural systems is further demonstrated by determining the ??13C and ??D values of petroleum hydrocarbons present in the Pawtuxet River, RI. Our results show that the combined SPMD-CSIA is an effective tool to investigate the source and fate of hydrophobic contaminants in the aquatic environments.

  9. Extraction of semivolatile organic compounds from high-efficiency particulate air (HEPA) filters by supercritical carbon dioxide

    Energy Technology Data Exchange (ETDEWEB)

    Schilling, J.B.

    1997-09-01

    Supercritical fluid extraction (SFE) using unmodified carbon dioxide has been explored as an alternative method for the extraction of semivolatile organic compounds from high-efficiency particulate air (HEPA) filters. HEPA filters provide the final stage of containment on many exhaust systems in US Department of Energy (DOE) facilities by preventing the escape of chemical and radioactive materials entrained in the exhausted air. The efficiency of the filters is tested by the manufacturer and DOE using dioctylphthalate (DOP), a substance regulated by the US Environmental Protection Agency under the Resource Conservation and Recovery Act. Therefore, the filters must be analyzed for semivolatile organics before disposal. Ninety-eight acid, base, and neutral semivolatile organics were spiked onto blank HEPA material and extracted using SFE, Soxhlet, automated Soxhlet, and sonication techniques. The SFE conditions were optimized using a Dionex SFE-703 instrument. Average recoveries for the 98 semivolatile compounds are 82.7% for Soxhlet, 74.0% for sonication, 70.2% for SFE, and 62.9% for Soxtec. Supercritical fluid extraction reduces the extraction solvent volume to 10--15 mL, a factor of 20--30 less than Soxhlet and more than 5 times less than Soxtec and sonication. Extraction times of 30--45 min are used compared to 16--18 h for Soxhlet extraction.

  10. MODIFIED SCREEN-PRINTED CARBON ELECTRODES WITH TYROSINASE FOR DETERMINATION OF PHENOLIC COMPOUNDS IN SMOKED FOOD

    Directory of Open Access Journals (Sweden)

    V. Dragancea

    2010-12-01

    Full Text Available A screen-printed carbon electrode modified with tyrosinase (SPCE-Tyr/Paa/Glut has been developed for the determination of phenol concentration in real samples. The resulting SPCE-Tyr/Paa/Glut was prepared in a one-step procedure, and was then optimized as an amperometric biosensor operating at 0 mV versus Ag/AgCl for phenol determination in flow injection mode. Phenol detection was realized by electrochemical reduction of quinone produced by tyrosinase activity. The possibility of using the developed biosensor to determine phenol concentrations in various smoked products (bacon, ham, chicken and salmon was also evaluated. Gas chromatography (GC method was used for result validation obtained in flow injection mode using amperometric biosensor. The result showed good correlation with those obtained by flowinjection analysis (FIA.

  11. Uranium value leaching with ammonium carbonate and/or bicarbonate plus nitrate oxidant and optionally oxidation-catalytic metal compounds

    International Nuclear Information System (INIS)

    In accordance with the present invention, uranium values are extracted from solid materials containing uranium in lower valence states than its hexavalent state comprising contacting the solid materials containing uranium with an alkaline leach solution containing the ionic species NH4+ and NO3- in an amount sufficient to convert at least a portion of the uranium in valence states lower than its hexavalent state to its hexavalent state. In another embodiment of the present invention, the aqueous alkaline leach solution is an aqueous solution of a carbonate selected from the group consisting of ammonium carbonate, ammonium bicarbonate and mixtures thereof. In a further embodiment, ionic species NO3- is supplied by an alkaline nitrate. In yet another embodiment of the present invention, the aqueous alkaline leach solution additionally contains at least one catalytic compound of a metal selected from the group consisting of copper, cobalt, iron, nickel, chromium and mixtures thereof adapted to assure the pesence of the ionic species Cu++, Co++, Fe+++, Ni++, Cr+++ and mixtures thereof, respectively, is present during the contacting of the solid materials containing uranium with the aqueous alkaline leach solution in an amount sufficient to catalyze the oxidation of at least a part of the uranium in valence states lower than its hexavalent state to its hexavalent state

  12. Adsorption onto Activated Carbon Fiber Cloth and Electrothermal Desorption of Volatile Organic Compound (VOCs): A Specific Review

    Institute of Scientific and Technical Information of China (English)

    Pierre Le Cloirec

    2012-01-01

    A general research program, focusing on activated carbon fiber cloths (ACFC) and felt for environmental protection was performed. The objectives were multiple: (i) a better understanding of the adsorption mecha- nisms of these kinds of materials; (ii) the specification and optimization of new processes using these adsorbents; (iii) the modeling of the adsorption of organic pollutants using both the usual and original approaches; (iv) applications of ACFC in industrial processes. The general question was: how can activated carbon fiber cloths and felts be used in air treatment processes for the protection of environment. In order to provide an answer, different approaches were adopted. The materials (ACFC) were characterized in terms of macro structure and internal porosity. Specific studies were performed to get the air flow pattern through the fabrics. Head loss data were generated and modeled as a fi.mction of air velocity. The performances of ACF to remove volatile organic compounds (VOCs) were approached with the adsorption isotherms and breakthrough curves in various operating conditions. Regenera- tion by Joule effect shows a homogenous heating of adsorber modules with rolled or pleated layers. Examples of industrial developments were presented showing an interesting technology for the removal of VOCs, such as dichloromethane, benzene, isopropyl alcohol and toluene, alone or in a complex mixture.

  13. In situ sorption of hydrophobic organic compounds to sediment amended with activated carbon

    International Nuclear Information System (INIS)

    Contaminated sediments can be remediated by adding carbonaceous materials (CM), e.g. activated carbons (AC). Here, we analyze published datasets from AC amendment trials to identify variation in the effectiveness of AC in reducing porewater concentrations of hydrophobic organic contaminants (HOCs). The analysis uses a model that separates the contribution of HOC sorption to AC by parameterzing the sorption contributions by amorphous organic matter and black carbon (BC). It appears that sorption to BC increased with LogKOW, whereas sorption to AC showed a relatively narrow range of affinity properties with a median Freundlich LogKF,AC value of 7.2 (μg/kgAC)/(μg/L)n (IQR = 7.0–7.5) for polychlorinated biphenyls (PCBs) and 8.6 (IQR = 8.3–8.8) for polycyclic aromatic hydrocarbons (PAHs). Estimated Freundlich exponents were nF,AC = 0.74 for PCBs and 0.82 for PAH. Sorption to AC was stronger than to BC for chemicals below LogKOW = 6.3–6.6. For HOC risk reduction this is favorable, because chemicals with low KOW show generally higher bioavailable concentrations. - Highlights: ► We provide a conceptual framework to assess affinity constants for HOC sorption to CM. ► We determined the affinity parameters for HOC sorption to BC and AC. ► HOC sorption to AC showed a narrow range of AC affinity properties. ► HOC sorption to AC was stronger than to BC for chemicals below LogKOW = 6.3–6.6. ► 1% of AC appears to be sufficient to reduce pore water concentration by 99%. - We analyzed datasets from AC amendment trials to identify the variation in AC effectiveness and to explore to what extent HOC binding to AC may be generalized.

  14. Compound-Specific Carbon and Hydrogen Isotope Analysis - Field Evidence of MTBE Bioremediation

    Science.gov (United States)

    Kuder, T.; Kolhatkar, R. V.; Philp, P.; Wilson, J. T.; Landmeyer, J. E.; Allen, J.

    2002-12-01

    Compound-specific stable isotope analysis allows opportunity to determine the isotopic ratios of individual contaminants. The technique has been applied to confirm biodegradation in studies of chlorinated solvents and recently BTEX, MTBE and TBA. Chemical reactions (including bio- and inorganic degradation) tend to favor molecules with the lighter isotopic species (e.g., 12C, 1H), resulting with enrichment of the unreacted substrate in the heavier isotopic species (13C, D), referred to as kinetic isotopic fractionation, so that the extent of fractionation may be used as a proxy for biodegradation. Processes such as volatilization, sorption etc., result in minimal degree of fractionation and do not interfere with the isotopic signal due to biodegradation. The results presented here show the first successful applications of compound-specific isotope analysis to understanding MTBE biodegradation in the field, at both aerobic and anaerobic sites. Observed fractionations suggest that two different biodegradation pathways may be involved. At a number of anaerobic locations major fractionation effects were observed for both C and H; enrichment factors Ÿnfor both elements were approaching or exceeding -10. A laboratory microcosm study using an enrichment culture yielded similar results (C data only). A characteristic feature of these sites was the presence of high concentrations of TBA. Conversely, at a number of sites, the C composition remained stable with little fractionation and stayed within the analytical precision range or changed minimally, while H displayed significant fractionation in excess of 60 per mil. Moderate agreement of the data with Rayleigh fractionation model was observed, suggesting that biodegradation effect was distorted by variability at the source or the plume was not homogeneous. The enrichment factor calculated for these data is similar to the one Ÿnpublished for aerobic microcosm of MTBE-degrading culture from Vandenberg AFB by Gray et al

  15. Analysis of preference for carbon source utilization among three strains of aromatic compounds degrading Pseudomonas.

    Science.gov (United States)

    Karishma, M; Trivedi, Vikas D; Choudhary, Alpa; Mhatre, Akanksha; Kambli, Pranita; Desai, Jinal; Phale, Prashant S

    2015-10-01

    Soil isolates Pseudomonas putida CSV86, Pseudomonas aeruginosa PP4 and Pseudomonas sp. C5pp degrade naphthalene, phthalate isomers and carbaryl, respectively. Strain CSV86 displayed a diauxic growth pattern on phenylpropanoid compounds (veratraldehyde, ferulic acid, vanillin or vanillic acid) plus glucose with a distinct second lag-phase. The glucose concentration in the medium remained constant with higher cell respiration rates on aromatics and maximum protocatechuate 3,4-dioxygenase activity in the first log-phase, which gradually decreased in the second log-phase with concomitant depletion of the glucose. In strains PP4 and C5pp, growth profile and metabolic studies suggest that glucose is utilized in the first log-phase with the repression of utilization of aromatics (phthalate or carbaryl). All three strains utilize benzoate via the catechol 'ortho' ring-cleavage pathway. On benzoate plus glucose, strain CSV86 showed preference for benzoate over glucose in contrast to strains PP4 and C5pp. Additionally, organic acids like succinate were preferred over aromatics in strains PP4 and C5pp, whereas strain CSV86 co-metabolizes them. Preferential utilization of aromatics over glucose and co-metabolism of organic acids and aromatics are found to be unique properties of P. putida CSV86 as compared with strains PP4 and C5pp and this property of strain CSV86 can be exploited for effective bioremediation. PMID:26316546

  16. Adsorption of odorous sulfur compounds onto activated carbons modified by gamma irradiation.

    Science.gov (United States)

    Vega, Esther; Sánchez-Polo, Manuel; Gonzalez-Olmos, Rafael; Martin, María J

    2015-11-01

    A commercial activated carbon (AC) was modified by gamma irradiation and was tested as adsorbent for the removal of ethyl mercaptan, dimethyl disulfide and dimethyl disulfide in wet conditions. Modifications were carried out under five different conditions: irradiation in absence of water, in presence of ultrapure water, in ultrapure water at pH=1.0 and 1000 mg L(-1) Cl(-), in ultrapure water at pH=7.5 and 1000 mg L(-1) Br(-), and in ultrapure water at pH=12.5 and 1000 mg L(-1) NO3(-). The chemical properties of each AC were characterized by elemental analysis, temperature programmed desorption and X-ray photoelectron spectroscopy. Outcomes show that a large number of oxygen functional groups were incorporated in the AC surface by gamma irradiation, especially in the AC irradiated in the presence of ultrapure water. The dynamic adsorption test results reveal that the incorporation of oxygen functional groups did not enhance the adsorption capacities for dimethyl sulfide and dimethyl disulfide. A significant improvement in the ethyl mercaptan adsorption capacity was correlated with the incorporation of phenolic groups in the AC surface. Moreover, diethyl disulfide was detected as by-product of ethyl mercaptan oxidation process under wet conditions and its formation depended on the chemical properties of ACs. PMID:26160734

  17. Hydrogen and carbon isotopic ratios of polycyclic aromatic compounds in two CM2 carbonaceous chondrites and implications for prebiotic organic synthesis

    Science.gov (United States)

    Huang, Yongsong; Aponte, José C.; Zhao, Jiaju; Tarozo, Rafael; Hallmann, Christian

    2015-09-01

    Study of meteoritic organic compounds offers a unique opportunity to understand the origins of the organic matter in the early Solar System. Meteoritic polycyclic aromatic hydrocarbons (PAHs) and heteropolycyclic aromatic compounds (HACs) have been studied for over fifty years, however; their hydrogen stable isotopic ratios (δD) have never been reported. Compound-specific δD measurements of PAHs and HACs are important, in part because the carbon isotopic ratios (δ13C) of various meteoritic PAHs cannot be readily distinguished from their terrestrial counterparts and it is difficult to rule out terrestrial contamination based on carbon isotopic ratios alone. In this study, we have extracted and identified more than sixty PAHs and HACs present in two CM2 carbonaceous chondrites Murchison and LON 94101. Their carbon and hydrogen stable isotopic ratios (δ13C and δD) were measured and used to discuss about their synthetic environments and formation mechanisms. The concentration of aromatic compounds is ∼30% higher in Murchison than in the Antarctic meteorite LON 94101, but both samples contained similar suites of PAHs and HACs. All PAHs and HACs found exhibited positive δD values (up to 1100‰) consistent with an extraterrestrial origin, indicating the relatively low δ13C values are indeed an inherent feature of the meteoritic aromatic compounds. The hydrogen isotopic data suggest aromatic compounds in carbonaceous chondrites were mainly formed in the cold interstellar environments. Molecular level variations in hydrogen and carbon isotopic values offer new insights to the formation pathways for the aromatic compounds in carbonaceous chondrites.

  18. Developing microbe-plant interactions for applications in plant-growth promotion and disease control, production of useful compounds, remediation, and carbon sequestration

    Energy Technology Data Exchange (ETDEWEB)

    Wu, C.H.; Bernard, S.; Andersen, G.L.; Chen, W.

    2009-03-01

    Interactions between plants and microbes are an integral part of our terrestrial ecosystem. Microbe-plant interactions are being applied in many areas. In this review, we present recent reports of applications in the areas of plant-growth promotion, biocontrol, bioactive compound and biomaterial production, remediation and carbon sequestration. Challenges, limitations and future outlook for each field are discussed.

  19. Selectivity of Chemoresistive Sensors Made of Chemically Functionalized Carbon Nanotube Random Networks for Volatile Organic Compounds (VOC

    Directory of Open Access Journals (Sweden)

    Jean-François Feller

    2014-01-01

    Full Text Available Different grades of chemically functionalized carbon nanotubes (CNT have been processed by spraying layer-by-layer (sLbL to obtain an array of chemoresistive transducers for volatile organic compound (VOC detection. The sLbL process led to random networks of CNT less conductive, but more sensitive to vapors than filtration under vacuum (bucky papers. Shorter CNT were also found to be more sensitive due to the less entangled and more easily disconnectable conducting networks they are making. Chemical functionalization of the CNT’ surface is changing their selectivity towards VOC, which makes it possible to easily discriminate methanol, chloroform and tetrahydrofuran (THF from toluene vapors after the assembly of CNT transducers into an array to make an e-nose. Interestingly, the amplitude of the CNT transducers’ responses can be enhanced by a factor of five (methanol to 100 (chloroform by dispersing them into a polymer matrix, such as poly(styrene (PS, poly(carbonate (PC or poly(methyl methacrylate (PMMA. COOH functionalization of CNT was found to penalize their dispersion in polymers and to decrease the sensors’ sensitivity. The resulting conductive polymer nanocomposites (CPCs not only allow for a more easy tuning of the sensors’ selectivity by changing the chemical nature of the matrix, but they also allow them to adjust their sensitivity by changing the average gap between CNT (acting on quantum tunneling in the CNT network. Quantum resistive sensors (QRSs appear promising for environmental monitoring and anticipated disease diagnostics that are both based on VOC analysis.

  20. Evaluating the interactions of organic compounds with multi-walled carbon nanotubes by self-packed HPLC column and linear solvation energy relationship

    International Nuclear Information System (INIS)

    Highlights: • The HPLC-based approach using CNTs as stationary phase is introduced. • The interactions of nine compounds to MWCNTs are evaluated by retention factors. • The LSER theory is adopted to probe the interactions of the compounds with MWCNTs. • π-/n-Electrons-dependent polarizable interaction plays a key role for adsorption. -- Abstract: Understanding the interactions between organic pollutants and carbon nanotubes (CNTs) is critical for fate assessment of both CNTs and organic pollutants. In this study, the chromatographic approach was introduced based on CNTs as stationary phase for the evaluation of such interactions. The pristine multi-walled carbon nanotubes (MWCNTs) were packed into columns of high-pressure liquid chromatography (HPLC) and the retention factors (k′) were determined to characterize the adsorption affinity of organic compounds onto MWCNTs. Nine compounds were tested. The results showed that their ln k′ values followed the order: benzene < toluene < phenol < chlorobenzene < bromobenzene < aniline < sulfamethoxazole < sulfadiazine ≈ sulfadimidine. The linear solvation energy relationship (LSER) theory was adopted to correlate ln k′ with the molecular solvatochromic parameters. We found that ln k′ of the studied compounds correlate positively with molecular polarizability (E) significantly, suggesting that the π-/n-electrons-dependent polarizable interactions play a major role for the adsorption. Moreover, the thermodynamic parameters calculated from van’t Hoff equations revealed that the interactions between the compounds and MWCNTs were spontaneous and exothermic processes

  1. Evaluating the interactions of organic compounds with multi-walled carbon nanotubes by self-packed HPLC column and linear solvation energy relationship

    Energy Technology Data Exchange (ETDEWEB)

    Chu, Yingqian; Li, Xuehua, E-mail: lixuehua@dlut.edu.cn; Xie, Hongbin; Fu, Zhiqiang; Yang, Xianhai; Qiao, Xianliang; Cai, Xiyun; Chen, Jingwen

    2013-12-15

    Highlights: • The HPLC-based approach using CNTs as stationary phase is introduced. • The interactions of nine compounds to MWCNTs are evaluated by retention factors. • The LSER theory is adopted to probe the interactions of the compounds with MWCNTs. • π-/n-Electrons-dependent polarizable interaction plays a key role for adsorption. -- Abstract: Understanding the interactions between organic pollutants and carbon nanotubes (CNTs) is critical for fate assessment of both CNTs and organic pollutants. In this study, the chromatographic approach was introduced based on CNTs as stationary phase for the evaluation of such interactions. The pristine multi-walled carbon nanotubes (MWCNTs) were packed into columns of high-pressure liquid chromatography (HPLC) and the retention factors (k′) were determined to characterize the adsorption affinity of organic compounds onto MWCNTs. Nine compounds were tested. The results showed that their ln k′ values followed the order: benzene < toluene < phenol < chlorobenzene < bromobenzene < aniline < sulfamethoxazole < sulfadiazine ≈ sulfadimidine. The linear solvation energy relationship (LSER) theory was adopted to correlate ln k′ with the molecular solvatochromic parameters. We found that ln k′ of the studied compounds correlate positively with molecular polarizability (E) significantly, suggesting that the π-/n-electrons-dependent polarizable interactions play a major role for the adsorption. Moreover, the thermodynamic parameters calculated from van’t Hoff equations revealed that the interactions between the compounds and MWCNTs were spontaneous and exothermic processes.

  2. Carbon doping of gallium arsenide and reflectance difference spectroscopy of compound semiconductors grown by metalorganic vapor-phase epitaxy

    Science.gov (United States)

    Begarney, Michael John

    The surface structure and chemistry of compound semiconductors used in heterojunction bipolar transistors was investigated. Lattice-matched, single crystal films of gallium arsenide and indium phosphide were deposited by metalorganic vapor-phase epitaxy in a horizontal-flow, quartz reactor. Two areas of the transistor fabrication process were studied: (1) carbon doping of the gallium arsenide base layer using carbon tetrachloride, and (2) in-situ monitoring of the surface reconstructions of gallium arsenide and indium phosphide by reflectance difference spectroscopy for improved heterointerface formation. Carbon tetrachloride was found to effect the growth of gallium arsenide in two ways: (1) reaction of chlorine with adsorbed gallium atoms to produce volatile GaCl, and (2) reaction of chlorine with the GaAs film to produce GaCl3. The latter of these reactions was found to be insignificant below a temperature-dependent threshold ratio of chlorine to gallium. At lower values of this ratio, step bunching and pinning was observed, while at higher values, pits ranging from 20 to 50 nm in diameter resulted. We show that these results arise due to the presence of the c(4 x 4) gallium arsenide reconstruction during crystal growth, and the site-specific adsorption of CCl4 at gallium atom sites, which are present only at step edges for this reconstruction. The relationship between the reflectance difference spectra and the atomic structure of arsenic-rich reconstructions of GaAs (001) were investigated. It was found that a roughening process, involving the desorption of arsenic and outdiffusion of gallium atoms to the surface, takes place as the surface structure changes with decreasing arsenic coverage. We determined that the intensity of the negative peak at 2.8 eV strongly depends on the presence of adsorbed alkyl groups and gallium atoms, while, by contrast, the intensity of the positive peak at 2.9 eV is directly proportional to the density of (2 x 4)-type dimers. We

  3. The chemistry of subcritical water reactions of a hardwood derived lignin and lignin model compounds with nitrogen, hydrogen, carbon monoxide and carbon dioxide

    Science.gov (United States)

    Hill Bembenic, Meredith A.

    collected solids from the CO reactions appeared to be the most reacted (i.e., the most changed from the unreacted lignin) according to solid state 13C-NMR analysis, and the widest variety of products (methoxy-substituted phenolic compounds) were obtained when using CO according to GC/MS analysis. Therefore, reactions with CO were completed that varied the initial reaction pressure (300, 500 and 800 psi) in order to elucidate the effects of CO pressure. Similar conversion (≈54--58%) and DCM-soluble liquid product yields (≈53--62%) were obtained for the different pressure reactions, but the reactions with an initial pressure of 500 psi had the greatest change in aromaticity from the unreacted lignin. Additional reactions between Organosolv lignin and H2O with CO (initial pressure of 500 psi) were conducted where the reaction time was varied (15, 30 and 60 min.) to determine the effect of reaction time. Longer reaction time (60 min.) appeared to inhibit conversion to low molecular weight compounds (i.e., conversion and DCM-soluble yields were lower at ≈53% and ≈28%, respectively). Solid state 13C-NMR of collected residues also showed that there are losses in carbons representative of both guaiacyl and syringyl components as reaction time increases, which may indicate that methoxy groups are being cleaved or the products are reacting with each other (i.e., repolymerization) to form high molecular weight compounds as reaction time is increased. The role of H2O and the gases during the baseline reactions and the expanded CO reactions is not intuitive based on the results, so reactions with lignin model compounds (i.e., aromatic aldehydes represented by vanillin and syringaldehyde, aromatic ketones represented by acetovanillone and acetosyringone, and aromatic ethers represented by dibenzyl ether and 2-phenethyl phenyl ether) were completed to study this. From these results, the suggested reaction pathway of Organosolv lignin reactions in subcritical H2O with and without

  4. Modern climate and vegetation variability recorded in organic compounds and carbon isotopic compositions in the Dianchi watershed.

    Science.gov (United States)

    Xu, Meina; Wang, Yanhua; Yang, Hao; Xie, Biao; Niu, Xiaoyin

    2015-09-01

    The aliphatic hydrocarbons distribution and compound-specific characteristics of carbon isotopic compositions in the sediments from the small catchment (197 km(2)) of the Dianchi watershed were investigated for identification of modern climate and vegetation variations in the study area. Results show that a regular bimodal n-alkanes distribution ranged from nC16 to nC33, with strong dominance at nC17 for short-chain n-alkanes and nC31 for long-chain n-alkanes. Mass chromatogram of total fatty acids also indicates corresponding mixed contribution of algae, hydrophilous non-emergent (C4 plants) and terrestrial plants (C3 plants) to sedimentary organic matter (OM). At the depth of -24 to -25 cm (early 1970s), nC31/nC17 and terrestrial to aquatic ratio of hydrocarbons (TAR) values decrease, suggesting a shift of OM origins from C3 terrestrial plants to algae-derived C4 plants. The highest water stage in 1971 was found to be recorded in the particle size (drought resulted in the excessive OM inputs to the watershed. PMID:25976326

  5. Influence of activated carbon preloading by EfOM fractions from treated wastewater on adsorption of pharmaceutically active compounds.

    Science.gov (United States)

    Hu, Jingyi; Shang, Ran; Heijman, Bas; Rietveld, Luuk

    2016-05-01

    In this study, the preloading effects of different fractions of wastewater effluent organic matter (EfOM) on the adsorption of trace-level pharmaceutically active compounds (PhACs) onto granular activated carbon (GAC) were investigated. A nanofiltration (NF) membrane was employed to separate the EfOM by size, and two GACs with distinct pore structures were chosen for comparison. The results showed that preloading with EfOM substantially decreased PhAC uptake of the GACs; however, comparable PhAC adsorption capacities were achieved on GACs preloaded by feed EfOM and the NF-permeating EfOM. This indicates that: (1) the NF-rejected, larger EfOM molecules with an expectation to block the PhAC adsorption pores exerted little impact on the adsorbability of PhACs; (2) the smaller EfOM molecules present in the NF permeate contributed mainly to the decrease in PhAC uptake, mostly due to site competition. Of the two examined GACs, the wide pore-size-distributed GAC was found to be more susceptible to EfOM preloading than the microporous GAC. Furthermore, among the fourteen investigated PhACs, the negatively charged hydrophilic PhACs were generally subjected to a greater EfOM preloading impact. PMID:26891356

  6. Calcium carbonate interaction analysis in polypropylene compounds and their impact on the formation of beta crystalline phase of this polymer

    International Nuclear Information System (INIS)

    The insertion of calcium carbonate (CaCO3) in polypropylene compound is a thoroughly known technique widely studied in the academic area and in the industry. Its wide application is due, mainly, to increase mechanical properties with low manufacturing cost. These improvements in this polymer make it more versatile and competitive compared to other expensive polymers. In this study, the incorporation of four types of CaCO3 from the same manufacturer were compared and the focus was on the size of this mineral filler. Furthermore, it was analyzed the interaction of graphitized polypropylene with maleic anhydride (PP-g-MA) in the same samples. All these samples were analyzed by WAXS and SEM. The physical properties of tensile strength and impact were also analyzed. It was observed from this study that the smallest CaCO3 produced with PP-g-MA resulted in better physical properties with the formation of a crystalline phase beta, as originally studied by other authors using other raw materials. (author)

  7. Linear solvation energy relationship for the adsorption of synthetic organic compounds on single-walled carbon nanotubes in water.

    Science.gov (United States)

    Ding, H; Chen, C; Zhang, X

    2016-01-01

    The linear solvation energy relationship (LSER) was applied to predict the adsorption coefficient (K) of synthetic organic compounds (SOCs) on single-walled carbon nanotubes (SWCNTs). A total of 40 log K values were used to develop and validate the LSER model. The adsorption data for 34 SOCs were collected from 13 published articles and the other six were obtained in our experiment. The optimal model composed of four descriptors was developed by a stepwise multiple linear regression (MLR) method. The adjusted r(2) (r(2)adj) and root mean square error (RMSE) were 0.84 and 0.49, respectively, indicating good fitness. The leave-one-out cross-validation Q(2) ([Formula: see text]) was 0.79, suggesting the robustness of the model was satisfactory. The external Q(2) ([Formula: see text]) and RMSE (RMSEext) were 0.72 and 0.50, respectively, showing the model's strong predictive ability. Hydrogen bond donating interaction (bB) and cavity formation and dispersion interactions (vV) stood out as the two most influential factors controlling the adsorption of SOCs onto SWCNTs. The equilibrium concentration would affect the fitness and predictive ability of the model, while the coefficients varied slightly. PMID:26854726

  8. Biomarkers and compound-specific stable carbon isotope of n-alkanes in crude oils from Eastern Llanos Basin, Colombia

    Science.gov (United States)

    Cortes, Jorge E.; Rincon, Jose M.; Jaramillo, Jose M.; Philp, R. Paul; Allen, Jon

    2010-03-01

    Representative samples of crude oils from Cusiana, Cupiagua, Apiay, Castilla and Chichimene fields in the Eastern Llanos Basin of Colombia were analyzed to determine its compound-specific stable carbon isotope composition (CSIA) using gas chromatography-isotopic ratio-mass spectrometry (GC-IRMS). GC-IRMS analyses of n-alkanes allowed differentiating between Cretaceous and Cretaceous/Tertiary oil samples. Cretaceous sourced samples have δ13C-enriched values than Cretaceous/Tertiary sourced samples; the heavier isotope composition of these samples is due to their major terrigenous organic matter input. Their isotope distribution patterns suggest significant algal and/or bacterial contribution (marine origin). The analysis of the n-alkane fractions by GC-IRMS confirms that the organic matter has marine origin in those samples from Cusiana, Cupiagua and Apiay while Castilla and Chichimene have marine origin with terrestrial inputs. The results were confirmed by gas chromatography/FID and gas chromatography/mass spectrometry (GC/MS). Basic geochemical composition show that samples from Cupiagua/Cusiana fields and Apiay/Castilla/Chichimene fields in the Llanos basin, Colombia present different characteristics reflecting a specific for each depositional environment.

  9. Poly(methyl methacrylate) and thiophene-coated single-walled carbon nanotubes for volatile organic compound discrimination

    Science.gov (United States)

    Muangrat, Worawut; Chodjarusawad, Thanawee; Maolanon, Rungroj; Pratontep, Sirapat; Porntheeraphat, Supanit; Wongwiriyapan, Winadda

    2016-02-01

    Poly(methyl methacrylate) (PMMA) and thiophene-coated single-walled carbon nanotubes (SWNTs) were fabricated for use in volatile organic compound (VOC) detection. Pristine SWNTs were separately coated with PMMA (PMMA/SWNTs) and thiophene (thiophene/SWNTs) by spin-coating. Pristine SWNTs showed the highest response to methanol, while PMMA/SWNTs enabled 5.4-fold improved dichloromethane detection and thiophene/SWNTs enabled 1.4-fold improved acetone detection compared with pristine SWNTs. The sensor response of PMMA/SWNTs to dichloromethane and that of thiophene/SWNTs to acetone can be attributed to the Hildebrand solubility parameter (HSP). The more similar the HSP, the higher the sensor response. The sensor response of pristine SWNTs to methanol is related to the diffusion coefficient and molecular size. The relationships between the vapor concentration and sensor response of PMMA/SWNTs to dichloromethane and thiophene/SWNTs to acetone are based on Henry’s adsorption isotherm, while that of pristine SWNTs to methanol is based on the Henry-clustering model. Principal component analysis (PCA) results show that dichloromethane, acetone, and methanol were successfully discriminated.

  10. Removal of pharmaceutical compounds from water by adsorption on activated carbon and degradation with ozone; Eliminacion de compuestos farmaceuticos de las aguas por adsorcion en carbon activado y degradacion con ozono

    Energy Technology Data Exchange (ETDEWEB)

    Sanchez Polo, M.; Prado Joya, G.; Rivera Utrilla, J.; Ferro Garcia, M. A.; Bautista Toledo, M. I.; Lopez Penalver, J. J.; Gomez Merlo de la fuente, C.

    2007-07-01

    The removal of pharmaceutical compounds from water, using nitroimidazoles as model compounds, by means of both adsorption on activated carbon and ozonization has been studied. The results obtained have shown that activated carbon presents a great efficiency to remove these contaminants from waters because: the adsorption kinetics is very fast, and it is not affected by diffusion problems; the maximum adsorption capacity is very high (400-96 mg/g); and the nitroimidazole adsorption capacity is enhanced in natural waters. Regarding to the ozonization process, a low reactivity of these compounds with ozone has been observed (k{sub 0}3{approx_equal}100 M{sup -}1 s{sup -}1) although, nevertheless, they present a high affinity to the hydroxyl radicals (k{sub O}H{approx_equal}10{sup 1}0 M{sup -}1s{sup -}1). (Author) 13 refs.

  11. Building-Related Symptoms among Office Employees Associated with Indoor Carbon Dioxide and Total Volatile Organic Compounds

    Directory of Open Access Journals (Sweden)

    Chung-Yen Lu

    2015-05-01

    Full Text Available This study investigated whether sick building syndrome (SBS complaints among office workers were associated with the indoor air quality. With informed consent, 417 employees in 87 office rooms of eight high-rise buildings completed a self-reported questionnaire for symptoms experienced at work during the past month. Carbon dioxide (CO2, temperature, humidity and total volatile organic compounds (TVOCs in each office were simultaneously measured for eight office hours using portable monitors. Time-averaged workday difference between the indoor and the outdoor CO2 concentrations (dCO2 was calculated as a surrogate measure of ventilation efficiency for each office unit. The prevalence rates of SBS were 22.5% for eye syndrome, 15.3% for upper respiratory and 25.4% for non-specific syndromes. Tiredness (20.9%, difficulty in concentrating (14.6%, eye dryness (18.7% were also common complaints. The generalized estimating equations multivariate logistic regression analyses showed that adjusted odds ratios (aORs and 95% confidence interval (CI per 100 ppm increase in dCO2 were significantly associated with dry throat (1.10, 95% CI = (1.00–1.22, tiredness (1.16, 95% CI = (1.04–1.29 and dizziness (1.22, 95% CI = (1.08–1.37. The ORs for per 100 ppb increases in TVOCs were also associated with upper respiratory symptoms (1.06, 95% CI = (1.04–1.07, dry throat (1.06, 95% CI = (1.03–1.09 and irritability (1.02, 95% CI = (1.01–1.04. In conclusion, the association between some SBS symptoms and the exposure to CO2 and total VOCs are moderate but may be independently significant.

  12. Geochemical identification of coal-sourced oils and interbedded shale-sourced oils as revealed by compound specific carbon isotopic analysis

    Institute of Scientific and Technical Information of China (English)

    2001-01-01

    To date, questions remain as to how to differen tiate between coal- and interbedded shale-sourced oils in coal measures. Based on the hypothesis that δ13C value of sedimentary organic matter is controlled by the depositional environment and productivities of biota grown in such depositional setting, this note examines compound specific carbon isotopic profiles from coal and interbedded shale extracts using the gas chromatography-isotope ratio mass spectrometry technique (GC/IRMS). The results show that compound specific carbon isotope values from coal extracts are enriched in 13C relative to that of interbedded shale extracts, and provide useful information in characterizing coal- and interbedded shale-sourced oils in coal measures. An example for its successful application from the Turpan Basin, Northwestern China is presented.

  13. Geochemical investigations into the retention of reactive carbon compounds for toxic heavy metals. Final report; Geochemische Untersuchungen zur Retention von reaktiven Kohlenstoffverbindungen fuer toxische Schwermetalle. Abschlussbericht

    Energy Technology Data Exchange (ETDEWEB)

    Kupsch, H.; Mansel, A.; Crustewitz, C.

    2003-03-01

    The composition, reactivity and stability of reactive organic carbon compounds adsorbed on geogenic matrices was investigated. The surface deposits of NOM and its dependence on geochemical parameters was investigated in selected geomatrices. The retention of toxic heavy metals on these surface deposits of NOM was investigated in consideration of the presence of hydroxy species and inorganic ligands. The investigations of the reactivity of the NOM species requires analyses of these compounds and of the heavy metals in the ultratracer region. This was possible by means of radiochemical methods that were further developed in the context of this project. Radioactive labeling of identified reactive carbon compounds, e.g. with radioactive iodine, on the one hand, and the use of radioactive Cu, Pb, Hg isotopes on the other hand enabled speciation analyses in the binary systems (heavy metal + geomatrix, heavy metal + reactive carbon compounds, reactive carbon compounds + geomatrix) and especially in the ternary system (heavy metal + geomatrix + reactive carbon compounds) in defined conditions. The special labelling techniques were a precondition for distribution measurements in the near-natural, low concentration range. (orig.) [German] Ziel des Projektes war es, mit der vorhandenen Analytik und Expertise die Zusammensetzung, die Reaktivitaet und die Stabilitaet der auf den geogenen Matrizes sorbierten reaktiven organischen Kohlenstoffverbindungen und die damit verbundenen Stoffumsaetze aufzuklaeren. An ausgewaehlten Geomatrizes wurde die Ausbildung von Oberflaechendepositen des NOM und deren Abhaengigkeit gegenueber geochemischen Parametern untersucht. Unter der Beruecksichtigung der Gegenwart von Hydroxyspezies und anorganischen Liganden wurde die Retention toxischer Schwermetalle an diesen Oberflaechendepositen des NOM untersucht. Die Untersuchungen zur Reaktivitaet der NOM-Spezies setzt eine Analytik dieser Verbindungen und der Schwermetalle im Ultraspurenbereich

  14. Study of carbon nitride compounds synthesised by co-implantation of 13C and 14N in copper at different temperatures

    International Nuclear Information System (INIS)

    Research highlights: → Simultaneous implantation of 13C and 14N in copper were performed to synthesise CNx compounds. → The formation of fullerene-like CNx compounds was highlighted by XPS and TEM. → Only about 20% of the implanted 14N atoms are contained in the FL CxNy structures. → The exceeding of implanted nitrogen precipitates in large N2 gas bubbles. → A growth model for the FL CxNy structures is proposed. - Abstract: Carbon nitride compounds have been synthesised in copper by simultaneous high fluence (1018 at. cm-2) implantation of 13C and 14N ions. During the implantation process, the substrate temperature was maintained at 25, 250, 350 or 450 deg. C. Depth profiles of 13C and 14N were determined using the non-resonant nuclear reactions (NRA) induced by a 1.05 MeV deuteron beam. The retained doses were deduced from NRA measurements and compared to the implanted fluence. The chemical bonds between carbon and nitrogen were studied as a function of depth and temperature by X-ray photoelectron spectroscopy (XPS). The curve fitting of C 1s and N 1s core level photoelectron spectra reveal different types of C-N bonds and show the signature of N2 molecules. The presence of nitrogen gas bubbles in copper was highlighted by mass spectroscopy. The structure of carbon nitride compounds was characterised by transmission electron microscopy (TEM). For that purpose, cross-sectional samples were prepared using a focused ion beam (FIB) system. TEM observations showed the presence of small amorphous carbon nitride 'nano-capsules' and large gas bubbles in copper. Based on our observations, we propose a model for the growth of these nano-objects. Finally, the mechanical properties of the implanted samples were investigated by nano-indentation.

  15. Coupling Noble Metals and Carbon Supports in the Development of Combustion Catalysts for the Abatement of BTX Compounds in Air Streams

    OpenAIRE

    Sergio Morales-Torres; Francisco Carrasco-Marín; Agustín F. Pérez-Cadenas; Francisco José Maldonado-Hódar

    2015-01-01

    The catalytic combustion of volatile organic compounds (VOCs) is one of the most important techniques to remove these pollutants from the air stream, but it should be carried out at the lowest possible temperature, saving energy and avoiding the simultaneous formation of nitrogen oxides (NOx). Under these experimental conditions, the chemisorption of water generated from VOCs combustion may inhibit hydrophilic catalysts. Nowadays, a wide variety of carbon materials is available to be used in ...

  16. The contribution of vehicular emission to the atmospheric concentrations of carbon compounds in the Metropolitan Area of Sao Paulo

    Science.gov (United States)

    Andrade, M.; Fornaro, A.; Miranda, R.; Ynoue, R. Y.; Freitas, E. D.; LAPAt-Laboratorio de Analise dos Processos Atmosfericos

    2013-05-01

    It is recognized that megacities have regional and global effects on climate, and that aerosols and Green House Gases (GHG) constitute the principal tracer of those effects. Such is the case in the Metropolitan Area of Sao Paulo (MASP), one of the largest mega-cities in the world. MASP has a population of almost 20 million inhabitants. The main source of air pollution is the transport sector. In this region, there are approximately 6.5 million passenger cars and commercial vehicles: 85% light duty, 3% heavy-duty diesel vehicles (diesel + 3% bio-diesel) and 12% motorcycles. Of the light duty vehicle, approximately 55% burn a mixture (v/v) of 78% gasoline with 22% ethanol (referred to as gasohol), 4% use hydrated ethanol (95% ethanol + 5% water), 38% flexible fuel vehicles capable of burning both gasohol as hydrated ethanol, and 2% use diesel. In average 50% of the fuel used in MASP is ethanol what brings the necessity of more studies to understand the formation of photochemical oxidants and secondary particles. According to the São Paulo State Environmental Protection Agency, 97% of carbon monoxide (CO), 85% of hydrocarbons (HC), 82% of nitrogen oxides (NOx), 36% of sulfur dioxide emitted, and 36% of all inhalable particulate matter (PM10) are emitted by the vehicular fleet. Concerning particles, 75% of the Fine Particle Concentration is related to the burning of fuel, mainly diesel. The fine particles are composed of Organic Carbon (40%), Black Carbon (30%), ions (15%) and metals. It is known that the soot is warming the climate and is important to the radiative balance. Another important driver to the radiative balance, the CO2 is mainly emitted by the transport sector, which is responsible for 57% of its emission. A comprehensive project under development has the objective of determine the role of MASP as the source of gaseous and particle compounds to the atmosphere of the region and in a mesoscale perspective. The project with funding from the São Paulo

  17. Composites of multi-walled carbon nanotubes with polypropylene and thermoplastic olefin blends prepared by melt compounding

    Science.gov (United States)

    Petrie, Kyle G.

    Composites of multi-walled carbon nanotubes (MWCNTs) with polypropylene (PP) and thermoplastic olefins (TPOs) were prepared by melt compounding. Two non-covalent functionalization methods were employed to improve nanotube dispersion and the resulting composite properties are reported. The first functionalization approach involved partial coating of the surface of the nanotubes with a hyperbranched polyethylene (HBPE). MWCNT functionalization with HBPE was only moderately successful in breaking up the large aggregates that formed upon melt mixing with PP. In spite of the formation of large aggregates, the samples were conductive above a percolation threshold of 7.3 wt%. MWCNT functionalization did not disrupt the electrical conductivity of the nanotubes. The composite strength was improved with addition of nanotubes, but ductility was severely compromised because of the existence of aggregates. The second method involved PP matrix functionalization with aromatic moieties capable of pi-pi interaction with MWCNT sidewalls. Various microscopy techniques revealed the addition of only 25 wt% of PP-g-pyridine (Py) to the neat PP was capable of drastically reducing nanotube aggregate size and amount. Raman spectroscopy confirmed improved polymer/nanotube interaction with the PP-g-Py matrix. Electrical percolation threshold was obtained at a MWCNT loading of approximately 1.2 wt%. Electrical conductivity on the order of 10 -2 S/m was achieved, suggesting possible use in semi-conducting applications. Composite strength was improved upon addition of MWCNTs. The matrix functionalization with Py resulted in a significant improvement in composite ductility when filled with MWCNTs in comparison to its maleic anhydride (MA) counterpart. Preliminary investigations suggest that the use of alternating current (AC) electric fields may be effective in aligning nanotubes in PP to reduce the filler loading required for electrical percolation. Composites containing MWCNT within PP

  18. PAH, BTEX, carbonyl compound, black-carbon, NO2 and ultrafine particle dynamometer bench emissions for Euro 4 and Euro 5 diesel and gasoline passenger cars

    Science.gov (United States)

    Louis, Cédric; Liu, Yao; Tassel, Patrick; Perret, Pascal; Chaumond, Agnès; André, Michel

    2016-09-01

    Although implementing Diesel particulate filters (DPF) and other novel aftertreatment technologies makes it possible to achieve significant reductions in particle mass emissions, it may induce the release of ultrafine particles and emissions of many other unregulated compounds. This paper focuses on (i) ultrafine particles, black carbon, BTEX, PAH, carbonyl compounds, and NO2 emissions from Euro 4 and Euro 5 Diesel and gasoline passenger cars, (ii) the influence of driving conditions (e.g., cold start, urban, rural and motorway conditions), and (iii) the impact of additive and catalysed DPF devices on vehicle emissions. Chassis dynamometer tests were conducted on four Euro 5 vehicles and two Euro 4 vehicles: gasoline vehicles with and without direct injection system and Diesel vehicles equipped with additive and catalysed particulate filters. The results showed that compared to hot-start cycles, cold-start urban cycles increased all pollutant emissions by a factor of two. The sole exception was NO2, which was reduced by a factor of 1.3-6. Particulate and black carbon emissions from the gasoline engines were significantly higher than those from the Diesel engines equipped with DPF. Moreover, the catalysed DPF emitted about 3-10 times more carbonyl compounds and particles than additive DPF, respectively, during urban driving cycles, while the additive DPF vehicles emitted 2 and 5 times more BTEX and carbonyl compounds during motorway driving cycles. Regarding particle number distribution, the motorway driving cycle induced the emission of particles smaller in diameter (mode at 15 nm) than the urban cold-start cycle (mode at 80-100 nm). The results showed a clear positive correlation between particle, black carbon, and BTEX emissions, and a negative correlation between particles and NO2.

  19. Determination of carbon in uranium and its compounds; Determinacion de carbono en uranio metal y sus compuestos

    Energy Technology Data Exchange (ETDEWEB)

    Perez-Garcia, M. M.

    1972-07-01

    This paper collects the analytical methods used our laboratories for the determination of carbon in uranium metal, uranate salts and the oxides, fluorides and carbides of uranium. The carbon is usually burned off in a induction or resistance oven under oxygen flow. The CO{sub 2} is collected in barite solution. Where it is backtitrated with potassium biphthalate. (Author)

  20. Comparison of bulk and compound-specific δ 13C analyses and determination of carbon sources to salt marsh sediments using n-alkane distributions (Maine, USA)

    Science.gov (United States)

    Tanner, Benjamin R.; Uhle, Maria E.; Mora, Claudia I.; Kelley, Joseph T.; Schuneman, Patrick J.; Lane, Chad S.; Allen, Evan S.

    2010-01-01

    Sources of sedimentary organic matter to a Morse River, Maine (USA) salt marsh over the last 3390 ± 60 RCYBP (Radiocarbon Years Before Present) are determined using distribution patterns of n-alkanes, bulk carbon isotopic analysis, and compound-specific carbon isotopic analysis. Marsh foraminiferal counts suggest a ubiquitous presence of high marsh and higher-high marsh deposits (dominated by Trochammina macrescens forma macrescens, Trochammina comprimata, and Trochammina inflata), implying deposition from ˜0.2 m to 0.5 m above mean high water. Distributions of n-alkanes show a primary contribution from higher plants, confirmed by an average chain length value of 27.5 for the core sediments, and carbon preference index values all >3. Many sample depths are dominated by the C 25 alkane. Salicornia depressa and Ruppia maritima have similar n-alkane distributions to many of the salt marsh sediments, and we suggest that one or both of these plants is either an important source to the biomass of the marsh through time, or that another unidentified higher plant source is contributing heavily to the sediment pool. Bacterial degradation or algal inputs to the marsh sediments appear to be minor. Compound-specific carbon isotopic analyses of the C 27 alkane are on average 7.2‰ depleted relative to bulk values, but the two records are strongly correlated ( R2 = 0.89), suggesting that marsh plants dominate the bulk carbon isotopic signal. Our study underscores the importance of using caution when applying mixing models of plant species to salt marsh sediments, especially when relatively few plants are included in the model.

  1. Simultaneous determination of phenolic compounds in sesame oil using LC-MS/MS combined with magnetic carboxylated multi-walled carbon nanotubes.

    Science.gov (United States)

    Wu, Rao; Ma, Fei; Zhang, Liangxiao; Li, Peiwu; Li, Guangming; Zhang, Qi; Zhang, Wen; Wang, Xiuping

    2016-08-01

    A novel magnetic carboxylated multi-walled carbon nanotubes (c-MWCNT-MNPs) was proposed for magnetic solid-phase extraction coupled with liquid chromatography-tandem mass spectrometry to determine phenolic compounds in sesame oil. In this study, c-MWCNT-MNPs were acquired by simply dispersing Fe3O4 magnetic nanoparticles into carboxylated multi-walled carbon nanotubes. The major parameters affecting extraction efficiency were optimized, including the type and volume of desorption solvents, extraction and desorption time, washing solution, and sorbent amount. The limit of quantifications and limit of detections were from 0.03μg/kg to 43.00μg/kg and from 0.01μg/kg to 13.60μg/kg, respectively. The recoveries of phenolic compounds in vegetable oils were in the range of 83.8-125.9% with inter-day and intra-day precisions of less than 13.2%. It was confirmed that this method was simple, rapid and reliable with an excellent potential for routine analysis of phenolic compounds in oil samples. PMID:26988510

  2. Influences of carbon concentration on crystal structures and ideal strengths of B2CxO compounds in the B-C-O system

    Science.gov (United States)

    Zhang, Meiguang; Yan, Haiyan; Zheng, Baobing; Wei, Qun

    2015-10-01

    The search for novel superhard materials with special structures and improved thermal stability and hardness remains considerably experimental and theoretical challenges. Recent reports proposed that higher carbon content in ternary B2CxO compounds, which are isoelectronic with diamond, would lead to increased strength and hardness. This notion was derived from the calculated elastic parameters and empirical hardness formulas based on structural and electronic properties of the equilibrium structures. In present work, we introduce three potential ultra-incompressible and thermodynamically stable B2CxO (x ≥ 2) phases via a systematic particle swarm optimization algorithm structure searches. By evaluating the trends of the crystal configuration, electronic structure, and mechanical properties as a function of the C concentration, it is found that the high carbon concentration benefits the formation of the sp3 C-C covalent bonds and leads to the enhanced elastic moduli and ideal strengths in these B2CxO compounds. Studies of strain-stress behavior at large deformation, however, indicate that all these B2CxO compounds possess substantially lower ideal shear strengths than those of diamond and c-BN, suggesting that they may not be intrinsically superhard.

  3. Plant secondary compounds and soil microbial processes in carbon and nitrogen cycling in relation to tree species

    OpenAIRE

    Kanerva, Sanna

    2007-01-01

    The aim of this study was to explore soil microbial activities related to C and N cycling and the occurrence and concentrations of two important groups of plant secondary compounds, terpenes and phenolic compounds, under silver birch (Betula pendula Roth), Norway spruce (Picea abies (L.) Karst) and Scots pine (Pinus sylvestris L.) as well as to study the effects of volatile monoterpenes and tannins on soil microbial activities. The study site, located in Kivalo, northern Finland, included ca....

  4. Synthesis of a sugar-organometallic compound 1,1 Prime -difurfurylferrocene and its microwave preparation of carbon/iron oxide nanocomposite

    Energy Technology Data Exchange (ETDEWEB)

    Zhao Shanyu, E-mail: syzhao65@gmail.com [School of Environmental and Safty Engineering, Changzhou University, Changzhou, Jiangsu 213164 (China); Department of Chemistry, Brown University, Providence, RI 02912-9108 (United States); Cooper, Daniel C. [Department of Chemistry, Brown University, Providence, RI 02912-9108 (United States); Xu, Haixun [Institute of Building Materials, Dalian University of Technology, Dalian, Liaoning 116024 (China); Zhu Pinghua [School of Environmental and Safty Engineering, Changzhou University, Changzhou, Jiangsu 213164 (China); Suggs, J. William, E-mail: j_suggs@brown.edu [Department of Chemistry, Brown University, Providence, RI 02912-9108 (United States)

    2013-01-01

    Graphical abstract: In order to synthesize a carbon-metal or metal oxide combination sphere, carbonaceous resource furfural was introduced, which was nucleophilic treated with 1,1 Prime -dilithioferrocene to form a sugar-organometallic compound: ferrocenyl monosaccharide derivative 1,1 Prime -difurfurylferrocene, which can be hydrothermally treated in a microwave reactor to give 300-500 nm microspheres with the {alpha}-Fe{sub 2}O{sub 3} or Fe{sub 3}O{sub 4} formed on the surface, which may be favorable for new magnetic materials preparation or instead of iron with other metal ions, versatile carbon/metal composites will be possibly synthesized for catalysis, drug delivery and magnetic uses. Highlights: Black-Right-Pointing-Pointer We synthesized 1,1 Prime -difurfurylferrocene by nucleophilic treating furfural with 1,1 Prime -dilithioferrocene. Black-Right-Pointing-Pointer 1,1 Prime -Difurfurylferrocene can be hydrothermally treated by microwave to give microspheres with iron oxides on the surface. Black-Right-Pointing-Pointer 1,1 Prime -Difurfurylferrocene has 2 reactive furanose units, which form carbonspheres and ferrocenyl can give iron oxides. Black-Right-Pointing-Pointer REDOX atmosphere influences the coating structures. - Abstract: In order to synthesize a carbon-metal or metal oxide combination sphere, carbonaceous resource furfural 1 was introduced, which was nucleophilic treated with 1,1 Prime -dilithioferrocene 2 to form a sugar-organometallic compound: ferrocenyl monosaccharide derivative 1,1 Prime -difurfurylferrocene 3. 1,1 Prime -Difurfurylferrocene 3 can be hydrothermally treated in a microwave reactor to give 300-500 nm microspheres with the {alpha}-Fe{sub 2}O{sub 3} or Fe{sub 3}O{sub 4} nanocrystals formed on the surface, which may be favorable for new magnetic materials preparation or instead of iron with other metal ions, versatile carbon/metal composites will be possibly synthesized for catalysis, drug delivery and magnetic uses.

  5. Coupling Noble Metals and Carbon Supports in the Development of Combustion Catalysts for the Abatement of BTX Compounds in Air Streams

    Directory of Open Access Journals (Sweden)

    Sergio Morales-Torres

    2015-04-01

    Full Text Available The catalytic combustion of volatile organic compounds (VOCs is one of the most important techniques to remove these pollutants from the air stream, but it should be carried out at the lowest possible temperature, saving energy and avoiding the simultaneous formation of nitrogen oxides (NOx. Under these experimental conditions, the chemisorption of water generated from VOCs combustion may inhibit hydrophilic catalysts. Nowadays, a wide variety of carbon materials is available to be used in catalysis. The behavior of these hydrophobic materials in the development of highly active and selective combustion catalysts is analyzed in this manuscript. The support characteristics (porosity, hydrophobicity, structure, surface chemistry, etc. and the active phase nature (noble metals: Pt, Pd and dispersion were analyzed by several techniques and the results correlated with the dual adsorptive and/or catalytic performance of the corresponding catalysts. The coupling of highly active phases and carbon materials (activated carbons, honeycomb coated monoliths, carbon aerogels, etc. with tuneable physicochemical properties leads to the complete abatement of benzene, toluene and xylenes (BTX from dilute air streams, being selectively oxidized to CO2 at low temperatures.

  6. Hydrothermal synthesis of nanocubes of sillenite type compounds for photovoltaic applications and solar energy conversion of carbon dioxide to fuels

    Energy Technology Data Exchange (ETDEWEB)

    Subramanian, Vaidyanathan; Murugesan, Sankaran

    2014-04-29

    The present invention relates to formation of nanocubes of sillenite type compounds, such as bismuth titanate, i.e., Bi.sub.12TiO.sub.20, nanocubes, via a hydrothermal synthesis process, with the resulting compound(s) having multifunctional properties such as being useful in solar energy conversion, environmental remediation, and/or energy storage, for example. In one embodiment, a hydrothermal method is disclosed that transforms nanoparticles of TiO.sub.2 to bismuth titanate, i.e., Bi.sub.12TiO.sub.20, nanocubes, optionally loaded with palladium nanoparticles. The method includes reacting titanium dioxide nanotubes with a bismuth salt in an acidic bath at a temperature sufficient and for a time sufficient to form bismuth titanate crystals, which are subsequently annealed to form bismuth titanate nanocubes. After annealing, the bismuth titanate nanocubes may be optionally loaded with nano-sized metal particles, e.g., nanosized palladium particles.

  7. Investigation and comparison of the electro-photo property of carbon-rich chain and cycle compounds

    International Nuclear Information System (INIS)

    We investigate the electron-photo property of molecular macrochain and macrocycle compounds, which are constructed with phenylene and acetylene. Their electronic transition spectra and the second hyperpolarizability coefficients are calculated using ab initio and semiempirical methods. The energy gaps for the chain and ring molecules are shown to have very different regularity. The electronic transition wavelengths for chain and ring compounds are estimated to be shorter than 400 nm. The average values of the second-order hyperpolarizability coefficients per molecular unit increase with increasing number of the units. The asymptotic values are extrapolated to be 5.15 and 3.93x105 a.u. for chain and cycle compounds, respectively. These results show that they can be a kind of promising third order NLO material with high hyperpolarizability as well as good transparency to visible light

  8. Report on compounds labelled with nitrogen-13 or carbon-11 used in cancer metabolic studies with quantitative two-dimensional scanning and pet tomography

    International Nuclear Information System (INIS)

    The use of compounds labelled with radionuclides of the elements commonly involved in metabolic processes (oxygen, carbon, nitrogen) is becoming important in the non-invasive study of organ and tumour function. The application of compounds labelled with 13N and 11C to the study of amino-acid metabolism and changes in vasculature following chemotherapy and radiation therapy is described. In particular, 13N-labelled L-glutamate has been found to be useful in visualizing a number of human tumours including osteogenic sarcoma, rhabdomyosarcoma, Ewing's sarcoma, malignant fibrous histiocytoma, pineal gland tumours, primitive neuroectodermal tumours, medulloblastoma and several other solid tumours. In patients with bone tumours, changes in 13N-L-glutamate scans during chemotherapy were found to correlate with changes in other clinical parameters, such as serum alkaline phosphatase, histology and 99Tcsup(m)-bone scans, thus indicating that labelled L-glutamate is potentially useful in evaluating the response of solid tumours to chemotherapy. Scans of patients and volunteers using 13N-L-glutamate and 13N-L-valine indicate that the L-amino acids may be useful in studies of metabolic processes in the liver, myocardium and pancreas. Red blood cells, labelled with 11C-carbon monoxide via inhalation of the radioactive gas, have been used to assess changes in tumour vascularity following radiation therapy. Alpha-aminoisobutyric acid labelled with 11C has been synthesized and its distribution in normal and tumour-bearing dogs has been studied. (author)

  9. Effect of graphite intercalation compounds in the interfacial zone on the mechanical and thermal properties of unidirectional carbon fiber reinforced spodumene composite

    International Nuclear Information System (INIS)

    The interface in unidirectional carbon-fiber-reinforced β-spodumene matrix composite (UD-Cf/β-spodumene) significantly affected the thermal conductivity characteristics and mechanical properties due to the presence of a multi-layer interface. The mechanical and thermal properties of UD-Cf/β-spodumene composites with and without a multi-layer interface have been studied. The measured thermal conductivities, flexural strength and fracture toughness of composites with a multi-layer interface were much better than those composites with a clear interface. Interfacial layers with a multi-layer morphology originated from the diffusion of lithium from the β-spodumene matrix to the surface of the carbon fiber, which led to the formation of graphite intercalation compounds. The mechanical properties and thermal conductivity of UD-Cf/β-spodumene hot pressed at 1350 and 1400 °C were enhanced due to the textured interfacial microstructure and high thermal conductivity of graphite intercalation compounds. The textured interface decomposed at 1450 °C, resulting in the formation of a “strong” interface. Inevitably, the mechanical properties and thermal conductivity decreased

  10. Organic carbon and sulphur compounds in wetland soils: insights on structure and transformation processes using K-edge XANES and NMR spectroscopy

    Science.gov (United States)

    Jokic, Aleksander; Cutler, Jeffrey N.; Ponomarenko, Elena; van der Kamp, Garth; Anderson, Darwin W.

    2003-07-01

    X-ray absorption near-edge structure (XANES) and nuclear magnetic resonance (NMR) spectroscopy were used in combination to characterize organic carbon structures in a series of wetland soils in Saskatchewan, and XANES spectroscopy was also used to examine sulphur speciation in the soils. The organic C contents of most of the wetland soils are consistently higher by a factor of two to five times compared to adjacent well-drained soils. NMR analyses indicate that the organic matter in the wetland soils consists of predominantly aliphatic structures such as carbohydrates and long chain poly(methylene) units which are refractory structures found in plant waxes. The poly(methylene) structures have a significant capacity to sorb nonpolar organic molecules. The phenolic OH and carboxyl group content of the wetland soils studied is an additional significant factor in their sequestering ability for heavy metals or pesticides. Carbon XANES spectroscopy shows that the surface (˜10 nm) layer of particulate organic matter has a structure dominated by aromatic, carbohydrate and carboxylic acid-like material apparently derived from partially degraded lignin and cellulose polymers which are adsorbed onto clay minerals. The aliphatic structures remaining in this surface layer are probably recalcitrant (poly)methylene units. At a depth of ˜100 nm, the aliphatic content significantly increases suggesting the presence of more labile structures. The presence of these more labile aliphatic compounds may be due to slow decomposition rates in the wet, often cool environments present and to the protective action of the more refractory components in the surface ˜10 nm of the organic matter. Drying of the wetlands, either by draining or as a result of climate change, is likely to result in the rapid decomposition of these labile organic structures releasing carbon dioxide. Our data indicate that the preservation of the organic carbon compounds in these soils is a result of their presence

  11. Long-stored soil carbon released by prehistoric land use: Evidence from compound-specific radiocarbon analysis on Soppensee lake sediments

    Science.gov (United States)

    Gierga, Merle; Hajdas, Irka; van Raden, Ulrike J.; Gilli, Adrian; Wacker, Lukas; Sturm, Michael; Bernasconi, Stefano M.; Smittenberg, Rienk H.

    2016-07-01

    Compound-specific radiocarbon (14C) analyses allow studying the fate of individual biomarkers in ecosystems. In lakes with small catchments, terrestrial biomarkers have the potential to be used for the dating of sediments that lack the traditionally targeted terrestrial macrofossils, if the specific organic compounds are deposited soon after production. On the other hand, if the biomarkers have been stored for a significant amount of time in the soils of the catchment before transported to the lake, their age can be used to reconstruct changes in average residence time of organic material on land through time. Here we present a study based on compound-specific 14C analysis of the sedimentary record of Lake Soppensee, Switzerland, targeting long-chain n-alkanes of exclusive terrigenous origin, and comparing them with sediment ages obtained by high-resolution macrofossil dating. Additionally, we measured 14C ages of bulk organic matter and carbonate samples to assess the hard water effect. Prior to 3100 cal BP n-alkanes had about the same age as the sediment or they were slightly older, indicating that the vast majority of the terrestrial organic carbon transported to the lake had a short residence time on land. In the samples younger than 3100 cal BP an increasing offset is observed, indicating liberation of old buried soil organic matter that must have accumulated over the previous millennia. Our results indicate that as long as stable ecosystem conditions have prevailed, the distribution and isotopic composition of the n-alkanes can be used as environmental proxies in small catchments with limited surface runoff, confirming a few earlier studies.

  12. Colloidal activated carbon for in-situ groundwater remediation--Transport characteristics and adsorption of organic compounds in water-saturated sediment columns.

    Science.gov (United States)

    Georgi, Anett; Schierz, Ariette; Mackenzie, Katrin; Kopinke, Frank-Dieter

    2015-08-01

    Colloidal activated carbon can be considered as a versatile adsorbent and carrier material for in-situ groundwater remediation. In analogy to other nanoremediation approaches, activated carbon colloids (ACC) can be injected into the subsurface as aqueous suspensions. Deposition of ACC on the sediment creates a sorption barrier against further spreading of hydrophobic pollutants. This study deals with the optimization of ACC and their suspensions with a focus on suspension stability, ACC mobility in saturated porous media and sorption efficiency towards organic contaminants. ACC with an appropriate particle size range (d50=0.8μm) were obtained from a commercial powdered activated carbon product by means of wet-grinding. Among the various methods tested for stabilization of ACC suspensions, addition of humic acid (HA) and carboxymethyl cellulose (CMC) showed the best results. Due to electrosteric stabilization by adsorption of CMC, suspensions remained stable even at high ACC concentrations (11gL(-1)) and conditions typical of very hard water (5mM divalent cations). Furthermore, CMC-stabilized ACC showed high mobility in a water-saturated sandy sediment column (filter coefficient λ=0.2m(-1)). Such mobility is a pre-requisite for in-situ installation of sorption or reaction barriers by simple injection-well or direct-push application of ACC suspensions. Column experiments with organic model compounds proved the efficacy of ACC deposits on sediment for contaminant adsorption and retardation under flow-through conditions. PMID:26070009

  13. Fabrication of the single-wall carbon nanotube compound polymer film electrode and the simultaneous electrochemical behavior of aminophenol isomers

    International Nuclear Information System (INIS)

    We describe a simple, rapid and selective voltammetry for simultaneous determination of electroactive isomers using nanometer composite electrode. The electrode was constructed by electropolymerization of 4-aminopyridine at single-wall carbon nanotubes modified glassy carbon electrode (SWNTs/POAPE). The configuration and electrochemical properties of SWNTs/POAPE were characterized by scanning electronic micrographs (SEM) and voltammetry. The SWNTs/POAPE showed an excellent electrocatalytic activity to the oxidation of aminophenol isomers and capability of determining three aminophenol isomers simultaneously. The oxidation peak potential difference between m-aminophenol and o-aminophenol was 416 mV, o-aminophenol and p-aminophenol 119 mV, indicating that the o-, m- and p-aminophenol could be identified entirely at the SWNTs/POAPE. The proposed electrode has been applied to the simultaneous voltammetric determination of aminophenol isomers in mixture without previous chemical or physical separations.

  14. High efficient acetalization of carbonyl compounds with diols catalyzed by novel carbon-based solid strong acid catalyst

    Institute of Scientific and Technical Information of China (English)

    2007-01-01

    The novel carbon-based acid catalyst has been applied to catalyzing the acetalization and ketalization. The results showed that the catalyst was very efficient with the average yield over 93%. The novel heterogeneous catalyst has the advantages of high activity, wide applicability even to 7-membered ring acetals, strikingly simple workup procedure, non-pollution, and reusability, which will contribute to the green process greatly.

  15. Removal of the hazardous, volatile, and organic compound benzene from aqueous solution using phosphoric acid activated carbon from rice husk

    OpenAIRE

    Yakout, Sobhy M

    2014-01-01

    Background Benzene is one of the most hazardous organic pollutants in groundwater. The removal of benzene from water is very important from a health point of view and for environmental protection. In this study, benzene adsorption kinetics was investigated using phosphoric acid activated carbon, prepared from rice husk. Results An initial rapid uptake of benzene was observed and became almost constant after 40 minutes of contact. Kinetic data was analyzed using pseudo first order, pseudo seco...

  16. Synthesis of carbon quantum dots and zinc oxide nanosheets by pyrolysis of novel metal–organic framework compounds

    International Nuclear Information System (INIS)

    Highlights: • Thermodynamic and kinetic analysis of porous MOFs. • One step synthesis of CQDs and ZnO nanosheets. • The coexistence of CQDs and ZnO nanosheets show strong ultraviolet emission. - Abstract: Here, the carbon quantum dots and zinc oxide nanosheets with novel superstructures are successfully synthesized simultaneously from a hydrothermal preparation and thermal decomposition of a porous precursor of metal–organic frameworks. Porous metal–organic frameworks are prepared by the hydrothermal process by using zinc nitrate hexahydrate, 4,4′-oxybisbenzoic acid and 4,4′-bipyridine as the starting materials. Fluorescence spectrophotometer, X-ray powder diffraction, transmission electron microscopy and high-resolution transmission electron microscopy were used to characterize the structure and property. The results show the coexistence of carbon quantum dots and zinc oxide nanosheets. The carbon quantum dots size is about 4 nm. Particularly, zinc oxide nanosheets show a new triangular sheet structure that has almost the same size. Strong ultraviolet emission of this coexistence system should be useful in developing visible light-emitting and nanophotonic devices

  17. Synthesis of carbon quantum dots and zinc oxide nanosheets by pyrolysis of novel metal–organic framework compounds

    Energy Technology Data Exchange (ETDEWEB)

    Ma, Qiliang; Zhang, Zhaochun, E-mail: zhangzhaochun@shu.edu.cn; Yu, Zhenwei

    2015-09-05

    Highlights: • Thermodynamic and kinetic analysis of porous MOFs. • One step synthesis of CQDs and ZnO nanosheets. • The coexistence of CQDs and ZnO nanosheets show strong ultraviolet emission. - Abstract: Here, the carbon quantum dots and zinc oxide nanosheets with novel superstructures are successfully synthesized simultaneously from a hydrothermal preparation and thermal decomposition of a porous precursor of metal–organic frameworks. Porous metal–organic frameworks are prepared by the hydrothermal process by using zinc nitrate hexahydrate, 4,4′-oxybisbenzoic acid and 4,4′-bipyridine as the starting materials. Fluorescence spectrophotometer, X-ray powder diffraction, transmission electron microscopy and high-resolution transmission electron microscopy were used to characterize the structure and property. The results show the coexistence of carbon quantum dots and zinc oxide nanosheets. The carbon quantum dots size is about 4 nm. Particularly, zinc oxide nanosheets show a new triangular sheet structure that has almost the same size. Strong ultraviolet emission of this coexistence system should be useful in developing visible light-emitting and nanophotonic devices.

  18. Organic carbon compounds detected by the SAM instrument suite on Curiosity: results of the first year of exploration at Gale Crater (Invited)

    Science.gov (United States)

    Summons, R. E.; Miller, K.; Glavin, D. P.; Eigenbrode, J. L.; Freissinet, C.; Martin, M. G.; Team, M.

    2013-12-01

    A search for organic matter is a high priority in the search for habitable environments on Mars as it is in the quest for clues about the nature of early life on Earth. These endeavors are technically challenging because of the inherent instability of organic matter under conditions that exist in the regolith of both planets and the antiquity of the sediments of interest. In the case of the early Earth, exposure to ionizing radiation and the heat associated with burial and tectonism are the main obstacles to organic matter preservation. On Mars, exposure to ionizing radiation and chemical oxidation are the prime threats to organic matter preservation. It has been hypothesized that UV-generated hydroxyl radicals will almost certainly oxidize or highly alter any organic carbon of martian or meteoritic origin at Mars' surface. Also, there could be diagenetic processes peculiar to Mars, for which no terrestrial analogs are presently known. Thus, the search for organics on Mars must be informed by data from the entire Curiosity payload since the results are mutually informative. Sediments from the Rocknest aeolian drift and the probable fluvio-lacustrine sediments of Yellowknife Bay in Gale Crater, when analyzed by pyrolysis with evolved gas analysis (EGA) and gas chromatography mass spectrometry (GC-MS), afforded a number of chlorohydrocarbons including chloromethane, dichloromethane, trichloromethane, a chloromethylpropene, and chlorobenzene (1, 2). Some proportion of these compounds can be traced to instrument background from organic materials within the chromatographic columns, hydrocarbon traps and wet chemistry capability of SAM. N-methyl-N-(tert-butyldimethylsilyl)trifluoroacetamide (MTBSTFA) and dimethylformamide, compounds carried in SAM for chemical derivatization can react with gases released from the sediments to yield the C1 and C4 chlorohydrocarbons. However, we continue to explore the possibility that a portion of the C1 chlorohydrocarbons are derived

  19. Terpenylic acid and nine-carbon multifunctional compounds formed during the aging of β-pinene ozonolysis secondary organic aerosol

    Science.gov (United States)

    Sato, Kei; Jia, Tianyu; Tanabe, Kiyoshi; Morino, Yu; Kajii, Yoshizumi; Imamura, Takashi

    2016-04-01

    Recent field and laboratory studies suggest that forest aerosol particles contain more highly functionalized organic molecules than pinonic acid, a traditional molecular maker of secondary organic aerosol (SOA) particles. To investigate the reaction mechanisms during the aging of biogenic SOAs, the gases and particles formed from the ozonolysis of β- and α-pinene were exposed to OH radicals in a laboratory chamber. The particle samples were collected before and after OH exposure for analysis by liquid chromatography-negative electrospray ionization time-of-flight mass spectrometry. Pinic acid and terpenylic acid were abundant products in both β- and α-pinene ozonolysis SOA particles. Terpenylic acid and products with m/z 201.08 present in β-pinene SOA particles increased upon exposing SOA to OH radicals, whereas 3-methyl-1,2,3-butanetricarboxylic acid present in α-pinene SOA particles increased upon exposing SOA to OH radicals. The products with m/z 201.08 were suggested to be C9H14O5 compounds. Similar C9H14O5 compounds and terpenylic acid were also detected in SOA particles formed from the photooxidation of nopinone, a major first-generation product of β-pinene ozonolysis. The OH-initiated oxidation of nopinone will contribute to the formation of terpenylic acid and C9H14O5 compounds during the aging of β-pinene SOA. A formation mechanism for terpenylic acid via gas-phase diaterpenylic acid formation followed by self-dehydration in the condensed phase was suggested.

  20. Development of new and improved labelling procedures for introducing isotopic hydrogen and carbon-11 into organic compounds

    International Nuclear Information System (INIS)

    New and improved methods for introducing radioisotopic hydrogen (tritium) and carbon (positron-emitting short-lived carbon-11, t1/2 = 20.4 min) into organic molecules for application in biological research have been explored. In Chapter 1 the applications of radioactive isotopes in biological and clinical research is surveyed, with particular emphasis on the value of β-emitting tritium and positron-emitting carbon-11. In Chapter 2 we report the use of the non-radioactive hydrogen isotope, deuterium, as a surrogate for tritium in the development of microwave-enhanced labelling procedures, based on catalytic hydrogen transfer to olefins (e.g. styrene, styrene derivatives, cinnamic acid and its derivatives). Hydrogen or deuterium donors (e.g. formate salts) were used alone or in combination with other sources (e.g. D2O). The method was found to give fully hydrogenated products using very short microwave irradiation times (∼ 2 min) and was highly reproducible. Importantly, the method is environmentally clean, as when extended to tritiated formates little or no radioactive waste is produced. In Chapter 3 we explored the labelling of CGP 62349 {3-[1-(R)-[3-(4-methoxybenzyl)phosphinyl-2-(S)-hydroxy-propyl- amino]ethyl]benzoic acid}, a γ-aminobutyric acid type B (GABAB) receptor antagonist, with carbon-11 in order to provide a prospective radioligand for medical imaging with positron emission tomography (PET). Labelling agents, [11C]iodomethane and [11C]methyl triflate, prepared by improved methods, were used in the rapid methylation of desmethyl-CGP 62349. Substantially higher radiochemical yields (78%) of [11C]CGP 62349 were achieved by the new methods compared to that produced in a previously published procedure (9%). In addition, the use of [11C]methyl triflate rather than [11C]iodomethane has the advantage of giving a high radiochemical yield and a lower amount of carrier. In Chapter 4 we report on the use of [11C]carbon monoxide as a labelling agent. This has

  1. Protective effect of compounds from the flowers of Citrus aurantium L. var. amara Engl against carbon tetrachloride-induced hepatocyte injury.

    Science.gov (United States)

    Lu, Qun; Yang, Li; Zhao, Hai-Yan; Jiang, Jian-Guo; Xu, Xi-Lin

    2013-12-01

    5-Hydroxy-6,7,3',4'-tetramethoxyflavone (HTF), limonexic acid (LA) are two compounds isolated from the flowers of Citrus aurantium L. var. amara Engl with various biological activities. This study was designed to investigate their protective effects against carbon tetrachloride (CCl4)-induced hepatocyte injury, using human hepatic cell line HL-7702 to determine the cell cytotoxicity, cell viability, levels of hepatic marker enzymes, malondialdehyde (MDA). Results showed that pretreatment with HTF, LA could significantly reverse CCl4-induced HL-7702 cell viability decrease, LA displayed a higher activity. HTF, LA also showed their capability of decreasing the CCl4-induced leakage of lactate dehydrogenase (LDH), aspartate aminotransferase (AST), inhibiting the lipid peroxidation, HTF showed more significant activity. Given that HTF, LA were not toxic, it is concluded that HTF, LA could effectively protect hepatocyte against CCl4-induced injury. PMID:23985451

  2. Effects of solution P H on the adsorption of aromatic compounds from aqueous solutions by activated carbon

    International Nuclear Information System (INIS)

    Absorption of p-Cresol, Benzoic acid and Nitro Benzene by activated carbon from dilute aqueous solutions was carried out under controlled ph conditions at 310 k. In acidic conditions, well below the pKa of all solutes, it was observed that the adsorbate solubility and the electron density of its aromatic ring were the influencing factors on the extent of the adsorption by affecting the extent of London dispersion forces. In higher solution ph conditions, on the other hand, it was found that the electrostatic forces played a significant role on the extent of adsorption. The Effect of ph must be considered from its combined effects on the carbon surface and on the solute molecules. It was found that the uptake of the molecular forms of the aromatic solutes was dependent on the substituents of the aromatic ring. Adsorption of the solutes in higher P H values was found to be dependent on the concentration of anionic form of the solutes. All isotherms were fitted into Freundlich Isotherm Equations

  3. Experimental validation of an effective carbon number-based approach for the gas chromatography-mass spectrometry quantification of 'compounds lacking authentic standards or surrogates'.

    Science.gov (United States)

    Kim, Yong-Hyun; Kim, Ki-Hyun; Szulejko, Jan E; Bae, Min-Suk; Brown, Richard J C

    2014-06-01

    For the quantitative analysis of 'compounds lacking authentic standards or surrogates' (CLASS) in environmental media, we previously introduced an effective carbon number (ECN) approach to develop an empirical equation for the prediction of their response factor (RF). In this research, a series of laboratory experiments were carried out to benchmark the reliability of an ECN approach for sorbent tube/thermal desorption/gas chromatography (GC)/mass spectrometry (MS) applications. First, the ECN values were determined using external calibration data from 25 reference volatile organic compounds (VOCs) using two MS dectectors (quadrupole (Q) and time-of-flight (TOF)). Then, a certified standard mixture of 54 VOCs was analyzed by each system as a simulated unknown sample. The analytical bias, assessed in terms of percentage difference (PD) between the certified and ECN-predicted mass values, averaged 19.2±16.1% (TOF-MS) and 28.2±27.6% (Q-MS). The bias using a more simplified carbon number (CN)-based prediction increased considerably, yielding 53.4±53.3% (TOF-MS) and 61.7±81.3% (Q-MS). However, the bias obtained using the ECN-based prediction decreased significantly to yield average PD values of 9.84±7.28% (TOF-MS) and 16.8±8.35% (Q-MS), if the comparison was limited to 26 (out of 54) VOCs with CN≥4 (i.e., 25 aromatics and hexachlorobutadiene). PMID:24856509

  4. Synthesis of a sugar-organometallic compound 1,1′-difurfurylferrocene and its microwave preparation of carbon/iron oxide nanocomposite

    International Nuclear Information System (INIS)

    Graphical abstract: In order to synthesize a carbon–metal or metal oxide combination sphere, carbonaceous resource furfural was introduced, which was nucleophilic treated with 1,1′-dilithioferrocene to form a sugar-organometallic compound: ferrocenyl monosaccharide derivative 1,1′-difurfurylferrocene, which can be hydrothermally treated in a microwave reactor to give 300–500 nm microspheres with the α-Fe2O3 or Fe3O4 formed on the surface, which may be favorable for new magnetic materials preparation or instead of iron with other metal ions, versatile carbon/metal composites will be possibly synthesized for catalysis, drug delivery and magnetic uses. Highlights: ► We synthesized 1,1′-difurfurylferrocene by nucleophilic treating furfural with 1,1′-dilithioferrocene. ► 1,1′-Difurfurylferrocene can be hydrothermally treated by microwave to give microspheres with iron oxides on the surface. ► 1,1′-Difurfurylferrocene has 2 reactive furanose units, which form carbonspheres and ferrocenyl can give iron oxides. ► REDOX atmosphere influences the coating structures. - Abstract: In order to synthesize a carbon–metal or metal oxide combination sphere, carbonaceous resource furfural 1 was introduced, which was nucleophilic treated with 1,1′-dilithioferrocene 2 to form a sugar-organometallic compound: ferrocenyl monosaccharide derivative 1,1′-difurfurylferrocene 3. 1,1′-Difurfurylferrocene 3 can be hydrothermally treated in a microwave reactor to give 300–500 nm microspheres with the α-Fe2O3 or Fe3O4 nanocrystals formed on the surface, which may be favorable for new magnetic materials preparation or instead of iron with other metal ions, versatile carbon/metal composites will be possibly synthesized for catalysis, drug delivery and magnetic uses.

  5. Nanoscale stabilization of zintl compounds: 1D ionic Li-P double helix confined inside a carbon nanotube

    Science.gov (United States)

    Ivanov, Alexander S.; Kar, Tapas; Boldyrev, Alexander I.

    2016-02-01

    One-dimensional (1D) ionic nanowires are extremely rare materials due to the difficulty in stabilizing 1D chains of ions under ambient conditions. We demonstrate here a theoretical prediction of a novel hybrid material, a nanotube encapsulated 1D ionic lithium monophosphide (LiP) chain, featuring a unique double-helix structure, which is very unusual in inorganic chemistry. This nanocomposite has been investigated with density functional theory, including molecular dynamics simulations and electronic structure calculations. We find that the formation of the LiP double-helical nanowire is facilitated by strong interactions between LiP and CNTs resulting in a charge transfer. This work suggests that nanostructured confinement may be used to stabilize other polyphosphide 1D chains, thus opening new ways to study the chemistry of zintl compounds at the nanoscale.One-dimensional (1D) ionic nanowires are extremely rare materials due to the difficulty in stabilizing 1D chains of ions under ambient conditions. We demonstrate here a theoretical prediction of a novel hybrid material, a nanotube encapsulated 1D ionic lithium monophosphide (LiP) chain, featuring a unique double-helix structure, which is very unusual in inorganic chemistry. This nanocomposite has been investigated with density functional theory, including molecular dynamics simulations and electronic structure calculations. We find that the formation of the LiP double-helical nanowire is facilitated by strong interactions between LiP and CNTs resulting in a charge transfer. This work suggests that nanostructured confinement may be used to stabilize other polyphosphide 1D chains, thus opening new ways to study the chemistry of zintl compounds at the nanoscale. Electronic supplementary information (ESI) available: Additional DOS, band structures, and Bader charges for LiP@SWCNTs. See DOI: 10.1039/c5nr07713c

  6. Additive effects of CuSO4 and aromatic compounds on laccase production by Pleurotus sajor-caju PS-2001 using sucrose as a carbon source

    Directory of Open Access Journals (Sweden)

    F. Bettin

    2014-06-01

    Full Text Available Laccase enzymes are now commercially available, and a laccase/mediator combination is currently marketed for indigo dye bleaching in textile manufacturing; replacing traditional chemical-based processes with enzymatic technology reduces the need for effluent treatment. However, an inexpensive source of these enzymes will be needed to enable wider application of this technology. In the present work, the main objective was to increase laccase production by the mushroom Pleurotus sajor-caju strain PS-2001 grown on sucrose derived from sugar cane, one of most economical carbon sources known, by the addition of compounds that are known to affect laccase production. High laccase activities (45-62 U mL-1 were obtained with additions of syringaldazine, benzoic acid, gallic acid, and vanillin. When CuSO4 was used in conjunction with these aromatic compounds, the levels of laccase activity were further improved, reaching 58-80 U mL-1. These laccase activities indicate the potential of this strain as an enzyme producer, which has also been detected in media containing glucose, but with activity lower than that observed with sucrose.

  7. Developing a Biologically-Inspired Molecular Solar Energy Conversion Device: Reaction of Solution and Protein-Bound Cobalamins with Carbon Dioxide and Halo-Organic Compounds

    Science.gov (United States)

    Robertson, Wesley D.; Ennist, Nathan M.; Warncke, Kurt

    2009-11-01

    Our aim is to design and construct protein-based artificial photosynthetic systems that reduce carbon dioxide (CO2) and toxic halo-organic compounds within the robust and adaptable (βα)8 TIM-barrel protein structure. The EutB subunit of the adenosylcobalamin-dependent enzyme, ethanolamine ammonia-lyase (EAL), from Salmonella typhimurium, was selected as the protein template. The Co^I forms of the native cobalamin (Cbl) cofactor and a derivative, cobinamide (Cbi), possess relatively low redox potentials that are commensurate with reduction of CO2 and halo-organic compounds. Titanium^III citrate and pulsed laser-excited 5'-deazariboflavin (5'-DRF) were used to reduce Cbl or Cbi. UV/visible absorption spectroscopy was used to monitor the reaction kinetics of reduced Cbl and Cbi with CO2 and halo-organics, and 13C-NMR was used for product analysis. The results provide fundamental information for development of an organocobalt-based protein-catalytic device for stable fuels generation and toxic chemical remediation.

  8. Effect of compounding process on the structure and electrochemical properties of ordered mesoporous carbon/polyaniline composites as electrodes for supercapacitors

    Science.gov (United States)

    Li, Lixia; Song, Huaihe; Zhang, Qincang; Yao, Jingyuan; Chen, Xiaohong

    Polyaniline (PANI) loaded ordered mesoporous carbon (OMC) composites were prepared via different processes, involving the in situ polymerization of aniline in the presence of OMC or its precursor and the direct physical mixing method. On the basis of analyzing the morphologies and structures of these three OMC/PANI composites, the influence of compounding processes on the electrochemical properties as electrodes for supercapacitors was first investigated. It was observed that regardless of compounding process, two distinct electrochemical behaviors took place on all of the composite electrodes, including a redox reaction with insertion and deinsertion of electrolyte ions, and electrostatic attraction at the electrode/electrolyte interface. Additionally, these OMC/PANI composites showed higher specific capacitances compared with pure OMC and PANI. Most significantly, the in situ synthesized OMC/PANI composite using OMC as a starting material exhibited the highest specific capacitance of 747 F g -1 at a current density of 0.1 A g -1 and excellent rate capability, which was attributed to the high degree of dispersion of PANI and the contact of PANI with electrolyte as well as the double fixing effects of surface and mesopore of OMC on PANI.

  9. Effect of compounding process on the structure and electrochemical properties of ordered mesoporous carbon/polyaniline composites as electrodes for supercapacitors

    Energy Technology Data Exchange (ETDEWEB)

    Li, Lixia; Song, Huaihe; Zhang, Qincang; Yao, Jingyuan; Chen, Xiaohong [State Key Laboratory of Chemical Resource Engineering, Beijing University of Chemical Technology, 100029 Beijing (China)

    2009-02-01

    Polyaniline (PANI) loaded ordered mesoporous carbon (OMC) composites were prepared via different processes, involving the in situ polymerization of aniline in the presence of OMC or its precursor and the direct physical mixing method. On the basis of analyzing the morphologies and structures of these three OMC/PANI composites, the influence of compounding processes on the electrochemical properties as electrodes for supercapacitors was first investigated. It was observed that regardless of compounding process, two distinct electrochemical behaviors took place on all of the composite electrodes, including a redox reaction with insertion and deinsertion of electrolyte ions, and electrostatic attraction at the electrode/electrolyte interface. Additionally, these OMC/PANI composites showed higher specific capacitances compared with pure OMC and PANI. Most significantly, the in situ synthesized OMC/PANI composite using OMC as a starting material exhibited the highest specific capacitance of 747 F g{sup -1} at a current density of 0.1 A g{sup -1} and excellent rate capability, which was attributed to the high degree of dispersion of PANI and the contact of PANI with electrolyte as well as the double fixing effects of surface and mesopore of OMC on PANI. (author)

  10. Field emission from carbon nanotube and tetrapod-like ZnO compound cathode fabricated by spin-coating method

    International Nuclear Information System (INIS)

    We present a study of the field emission properties of a mixture of multi-wall carbon nanotubes (MWCNTs) and tetrapod-like zinc oxide nanostructures (ZTPNs). A spin-coating process instead of screen-printing was used to fabricate the cathode; this prevented largely the destruction of the slim needles of ZTPNs by mechanical rubbing. The protruding needles of ZTPNs in the paste are largely responsible for the field emission, while the CNTs have been added to improve the conductivity of cathode. Ultra low turn-on field at 0.6 V/μm and threshold field at 1.5 V/μm were obtained; moreover, the emission uniformity improved substantially compared to unmixed samples of ZTPN.

  11. Preparation and Eh-pH diagrams of Fe(II)-Fe(III) green rust compounds; hyperfine interaction characteristics and stoichiometry of hydroxy-chloride, -sulphate and -carbonate

    International Nuclear Information System (INIS)

    Fe(II)-Fe(III) hydroxy-chloride, -sulphate and -carbonate were prepared by oxidation of a ferrous hydroxide precipitate in anion-containing aqueous solutions. The compounds are characterized by monitoring the redox potential Eh and the pH of stochiometric suspension vs time with the appropriate concentration ratios. X-ray diffraction allows us to characterize the crystal structure by distinguishing 'green rust one' (GR1) from 'green rust two' (GR2). Since green rusts (GRs) are of a pyroaurite-sjoegrenite-like structure, i.e., consisting of intercalated foreign anions and water molecules in the interlayers between the brucite-like layers of Fe(OH)2, their chemical formulae can be determined from the Moessbauer spectra. Three quadrupole doublets are observed: D1 and D2 correspond to a ferrous state with isomershift IS of about 1.27 mm s-1 and quadrupole splittings QS of about 2.85 and 2.60 mm s-1, respectively, whereas D3 corresponds to a ferric state with IS and QS of about 0.4 mm s-1. The hyperfine parameters of these doublets are similar from one green rust to another but their intensity ratios vary considerably. Finally, Eh and pH equilibrium diagrams of the Fe species in the presence of chloride, sulphate and carbonate anions contained within the water solution are drawn and the thermodynamic conditions of existence and degrees of oxidation of green rusts are discussed

  12. Single-walled carbon nanohorns immobilized on a microporous hollow polypropylene fiber as a sorbent for the extraction of volatile organic compounds from water samples

    International Nuclear Information System (INIS)

    We have evaluated the behavior of single-walled carbon nanohorns as a sorbent for headspace and direct immersion (micro)solid phase extraction using volatile organic compounds (VOCs) as model analytes. The conical carbon nanohorns were first oxidized in order to increase their solubility in water and organic solvents. A microporous hollow polypropylene fiber served as a mechanical support that provides a high surface area for nanoparticle retention. The extraction unit was directly placed in the liquid sample or the headspace of an aqueous standard or a water sample to extract and preconcentrate the VOCs. The variables affecting extraction have been optimized. The VOCs were then identified and quantified by GC/MS. We conclude that direct immersion of the fiber is the most adequate method for the extraction of VOCs from both liquid samples and headspace. Detection limits range from 3.5 to 4.3 ng L−1 (excepted for toluene with 25 ng L−1), and the precision (expressed as relative standard deviation) is between 3.9 and 9.6 %. The method was applied to the determination of toluene, ethylbenzene, various xylene isomers and styrene in bottled, river and tap waters, and the respective average recoveries of spiked samples are 95.6, 98.2 and 86.0 %. (author)

  13. Molecular distributions and compound-specific stable carbon isotopic compositions of lipids in wintertime aerosols from Beijing

    Science.gov (United States)

    Ren, Lujie; Fu, Pingqing; He, Yue; Hou, Juzhi; Chen, Jing; Pavuluri, Chandra Mouli; Sun, Yele; Wang, Zifa

    2016-01-01

    Molecular distributions and stable carbon isotopic compositions (δ13C) of n-alkanes, fatty acids and n-alcohols were investigated in urban aerosols from Beijing, northern China to better understand the sources and long-range atmospheric transport of terrestrial organic matter during polluted and clear days in winter. n-Alkanes (C19–C36), fatty acids (C8–C32) and n-alcohols (C16–C32) detected in Beijing aerosols are characterized by the predominance of C23, C16 and C28, respectively. Carbon preference index (CPI) values of n-alkanes, the ratios of the sum of odd-numbered n-alkanes to the sum of even-numbered n-alkanes, are close to 1, indicating a heavy influence of fossil fuel combustion. Relatively higher ratios of C(18:0+16:0)/C(18:n+16:1) (fatty acids) on clear days than polluted days indicate that long-distance transport and/or photochemical aging are more significant during clear days. δ13C values of n-alkanes and low molecular weight fatty acids (C16:0, C18:0) ranged from –34.1 to −24.7% and −26.9 to −24.6%, respectively, which are generally heavier on polluted days than those on clear days. Such a wide range suggests that atmospheric lipids in Beijing aerosols originate from multiple sources and encounter complicated atmospheric processes during long-range transport in North China. PMID:27270951

  14. Molecular distributions and compound-specific stable carbon isotopic compositions of lipids in wintertime aerosols from Beijing

    Science.gov (United States)

    Ren, Lujie; Fu, Pingqing; He, Yue; Hou, Juzhi; Chen, Jing; Pavuluri, Chandra Mouli; Sun, Yele; Wang, Zifa

    2016-06-01

    Molecular distributions and stable carbon isotopic compositions (δ13C) of n-alkanes, fatty acids and n-alcohols were investigated in urban aerosols from Beijing, northern China to better understand the sources and long-range atmospheric transport of terrestrial organic matter during polluted and clear days in winter. n-Alkanes (C19–C36), fatty acids (C8–C32) and n-alcohols (C16–C32) detected in Beijing aerosols are characterized by the predominance of C23, C16 and C28, respectively. Carbon preference index (CPI) values of n-alkanes, the ratios of the sum of odd-numbered n-alkanes to the sum of even-numbered n-alkanes, are close to 1, indicating a heavy influence of fossil fuel combustion. Relatively higher ratios of C(18:0+16:0)/C(18:n+16:1) (fatty acids) on clear days than polluted days indicate that long-distance transport and/or photochemical aging are more significant during clear days. δ13C values of n-alkanes and low molecular weight fatty acids (C16:0, C18:0) ranged from –34.1 to ‑24.7% and ‑26.9 to ‑24.6%, respectively, which are generally heavier on polluted days than those on clear days. Such a wide range suggests that atmospheric lipids in Beijing aerosols originate from multiple sources and encounter complicated atmospheric processes during long-range transport in North China.

  15. Organic Carbon Delivery to a High Arctic Watershed over the Late Holocene: Insights from Plant Biomarkers and Compound Specific δ13C and Δ14C Measurements

    Science.gov (United States)

    Schreiner, K. M.; Bianchi, T. S.; Eglinton, T. I.; Allison, M. A.

    2012-12-01

    The Colville River in Alaska is the largest river in North America which has a drainage basin that is exclusively underlain by permafrost, and as such provides a unique signal of historical changes in one of the world's most vulnerable areas to climate changes. Additionally, the Colville flows into Simpson's Lagoon, an area of the Alaskan Beaufort coast protected by a barrier island chain, lessening the impacts of Arctic storms and ice grounding on sediment mixing. Cores collected from the Colville river delta in August of 2010 were found to be composed of muddy, organic-rich, well-laminated sediments. The 2.5 to 3 meter length of each core spans about one to two thousand years of Holocene history, including the entire Anthropocene and much of the late Holocene. Two cores were sampled for this data set - one from close to the river mouth, and one from farther east in Simpson's Lagoon. Samples were taken every 2 cm for the entire length of both cores. In order to determine how the amount of terrestrial organic matter input changed over the Holocene, bulk analyses including percent organic carbon, percent nitrogen, and stable carbon isotopic analysis were performed, and biomarkers including lignin-phenols and fatty acids were measured. It was shown that lignin-phenol input is positively correlated with Alaskan North Slope temperature reconstructions. To determine whether the source of this increased terrestrial organic matter input was from fresh vegetation (for example, shrub encroachment onto tundra areas) or aged soil organic matter (potentially due to permafrost thawing and breakdown), selected samples were analyzed for compound-specific δ13C and Δ14C of fatty acids and lignin-phenols. These analyses show significant changes in carbon storage and in terrestrial carbon delivery to the Lagoon over time. These results represent the first fine-scale organic biomarker study in a high Arctic North American Lagoon, and have many implications for the future of carbon

  16. Hot and Dry Cleaning of Biomass-Gasified Gas Using Activated Carbons with Simultaneous Removal of Tar, Particles, and Sulfur Compounds

    Directory of Open Access Journals (Sweden)

    Kinya Sakanishi

    2012-05-01

    Full Text Available This study proposes a gas-cleaning process for the simultaneous removal of sulfur compounds, tar, and particles from biomass-gasified gas using Fe-supported activated carbon and a water-gas shift reaction. On a laboratory scale, the simultaneous removal of H2S and COS was performed under a mixture of gases (H2/CO/CO2/CH4/C2H4/N2/H2S/COS/steam. The reactions such as COS + H2 → H2S + CO and COS + H2O → H2S + CO2 and the water-gas shift reaction were promoted on the Fe-supported activated carbon. The adsorption capacity with steam was higher than that without steam. On a bench scale, the removal of impurities from a gas derived from biomass gasification was investigated using two activated filters packed with Fe-supported activated carbon. H2S and COS, three- and four-ring polycyclic aromatic hydrocarbons (PAHs, and particles were removed and a water-gas shift reaction was promoted through the first filter at 320–350 °C. The concentrations of H2S and COS decreased to less than 0.1 ppmv. Particles and the one- and two-ring PAHs, except for benzene, were then removed through the second filter at 60–170 °C. The concentration of tar and particles decreased from 2428 to 102 mg Nm−3 and from 2244 to 181 mg Nm−3, respectively.

  17. Carbon and nitrogen compounds and emission of greenhouse gases in ancient and modern soils of the Arkaim Reserve in the Steppe Trans-Ural Region

    Science.gov (United States)

    Inubushi, K.; Prikhodko, V. E.; Nagano, Kh.; Manakhov, D. V.

    2015-12-01

    Carbon and nitrogen compounds and the emission of CO2, CH4, and N2O were studied in the ancient buried and modern background soils developed from different parent materials in the Arkaim Reserve of Chelyabinsk oblast. The studies were performed after an 18-year-long period of absence of anthropogenic loads on the local ecosystems. Element contents in the humus horizons of the chernozems of the former plowland and pastures and of the forest soil reach 28-45.6 g/kg for Corg, 2.5-4.5 g/kg for Ntot, 140-423 mg/kg for labile carbon (Cl), 32-73 mg/kg for labile nitrogen (Nl), 350-952 mg/kg for carbon of microbial biomass (Cmic), and 38-85 mg/kg for nitrogen of microbial biomass (Nmic). The contents of different forms of C and N depend on the soil type and texture and on the type of land use, including that before reservation of the territory. The emission of greenhouse gases was examined in this area for the first time. The production of CO2 by the soil buried about 4000 years ago is an order of magnitude lower than that by the modern soil. The emission and sink of N2O are small in both modern and ancient soils. The behavior of methane is clearly different in the automorphic and hydromorphic soils: the former serve as methane sinks, whereas the latter act as methane sources. The rate of the CO2 emission from the soils is controlled by many factors, including the soil type, texture, degree of hydromorphism, composition of parent materials, and type of land use.

  18. The origin of branched GDGTs in lake environments: Tracing allochthonous and autochthonous sources using compound-specific carbon isotope analysis

    Science.gov (United States)

    Weber, Yuki; De Jonge, Cindy; Hopmans, Ellen C.; Sinninghe Damsté, Jaap S.; Gilli, Adrian; Lehmann, Moritz F.; Niemann, Helge

    2015-04-01

    Branched glycerol dialkyl glycerol tetraethers (brGDGTs) are bacterial membrane lipids that are ubiquitous in soils and peat, as well as in sediments and suspended particulate matter (SPM) of lakes, rivers and coastal marine environments. It has been found that the relative distribution of brGDGTs changes systematically with ambient temperature and pH, making them promising proxy indicators for paleoclimatic reconstructions in sedimentary archives. In lacustrine deposits, it was initially assumed that brGDGTs mainly originate from allochthonous soil organic matter, thus reflecting the integrated mean annual air temperature (MAAT) within the watershed. Most recent research, however, strongly suggest that the brGDGTs used for paleo-thermometry can also be produced in situ within the lake system, offsetting the temperature-brGDGT relationships commonly known from soils. Until now, disentangling the relative contribution of allochthonous versus autochthonous brGDGT sources in lacustrine sediments was impossible, complicating the use of brGDGTs for quantitative paleotemperature reconstructions. We recently discovered a novel brGDGT isomer with a strongly 13C-depleted carbon isotope composition of about 46.6 o in sediments of a small eutrophic Alpine lake (Lake Hinterburg, Switzerland), which was not present in soils collected from the catchment. Furthermore, all other major brGDGTs in the sediment uniformly displayed δ13C values of about 43 o strongly contrasting the C-isotopic composition of brGDGTs from catchment soils (ca. 27 ). These findings raise two prime questions: (1) Are lake-derived brGDGTs generally more depleted in 13C with respect to their allochthonous counterparts? (2) Does the δ13C of sedimentary brGDGTs serve as a reliable indicator for lacustrine in situ production of brGDGTs? To address these questions, we determined the 13C content of brGDGTs in surface sediments from various lakes across the Swiss Alps by CG-IRMS analysis of their alkyl chains

  19. Carbon tetrachloride contamination, 200 West Area, Hanford Site: Arid Site Integrated Demonstration for remediation of volatile organic compounds

    International Nuclear Information System (INIS)

    The Arid State Integrated Demonstration is a US Department of Energy (DOE) program targeted at the acquisition, development, demonstration, and deployment of technologies for evaluation and cleanup of volatile organic and associated contaminants in soils and ground waters. Several DOE laboratories, universities, and industry will participate in the program. Candidate technologies will be demonstrated in the areas of site characterization; performance prediction, monitoring, and evaluations; contaminant extraction and ex situ treatment; in situ remediations; and site closure and monitoring. The performance of these demonstrated technologies will be compared to baseline technologies and documented to promote the transfer of new technologies to industry for use at DOE facilities. The initial host site is the Hanford Site's 200 West Area. The location of the demonstration contains primarily carbon tetrachloride (CCl4), chloroform, and a variety of associated mixed waste contaminants. Chemical processes used to recover and purify plutonium at Hanford's plutonium finishing plant (Z Plant) resulted in the production of actinide-bearing waste liquid. Both aqueous and organic liquid wastes were generated, and were routinely discharged to subsurface disposal facilities. The primary radionuclide in the waste streams was plutonium, and the primary organic was CCl4. This paper contains brief descriptions of the principal CCl4 waste disposal facilities in Hanford's 200 West Area, associated hydrogeology, existing information on the extent of soil and ground-water contamination, and a conceptual outline of suspected subsurface CCl4 distributions

  20. Compound-specific stable carbon isotopic composition of petroleum hydrocarbons as a tool for tracing the source of oil spills

    International Nuclear Information System (INIS)

    With the increasing demand for and consumption of crude oils, oil spill accidents happen frequently during the transportation of crude oils and oil products, and the environmental hazard they pose has become increasingly serious in China. The exact identification of the source of spilled oil can act as forensic evidence in the investigation and handling of oil spill accidents. In this study, a weathering simulation experiment demonstrates that the mass loss of crude oils caused by short-term weathering mainly occurs within the first 24 h after a spill, and is dominated by the depletion of low-molecular weight hydrocarbons (18n-alkanes). Short-term weathering has no significant effect on δ13C values of individual n-alkanes (C12-C33), suggesting that a stable carbon isotope profile of n-alkanes can be a useful tool for tracing the source of an oil spill, particularly for weathered oils or those with a relatively low concentration or absence of sterane and terpane biomarkers

  1. Decomposition of plant-sourced carbon compounds by heterotrophic betaproteobacteria isolated from a tropical Costa Rican bromeliad.

    Science.gov (United States)

    Klann, Jane; McHenry, Alexandra; Montelongo, Carin; Goffredi, Shana K

    2016-06-01

    Betaproteobacteria were the most common isolates from the water-filled tank of a Costa Rican bromeliad. Isolates included eight species from the orders Neisseriales and Burkholderiales, with close relatives recovered previously from tropical soils, wetlands, freshwater, or in association with plants. Compared to close relatives, the isolates displayed high temperature and comparatively low pH optima, reflecting the tropical, acidic nature of the bromeliad tank. Bromeliad-associated bacteria most closely related to Chromobacterium, Herbaspirillum, and Aquitalea were all isolated exclusively at pH 6, while Ralstonia, Cupriavidus, and three species of Burkholderia were isolated mostly at pH 4. Activity profiles for the isolates suggest pervasive capabilities for the breakdown of plant-sourced organics, including d-galacturonic acid, mannitol, d-xylose, and l-phenylalanine, also reflecting a niche dominated by decomposition of leaves from the overlying canopy, which become entrained in the tanks. Metabolic activity profiles were overlapping between the Burkholderiales, isolated at pH 4, and the Neisseriales, isolated at pH 6, suggesting that plant material decomposition, which is presumably the underlying process sustaining the tank community and possibly the plant itself, occurs in the tanks at both pH extremes. These results suggest that bromeliad-associated betaproteobacteria may play an important role in the cycling of carbon in this unusual aquatic habitat. PMID:26918550

  2. Occupational exposure to complex mixtures of volatile organic compounds in ambient air: desorption from activated charcoal using accelerated solvent extraction can replace carbon disulfide?

    Science.gov (United States)

    Fabrizi, Giovanni; Fioretti, Marzia; Rocca, Lucia Mainero

    2013-01-01

    A desorption study of 57 volatile organic compounds (VOCs) has been conducted by use of accelerated solvent extraction (ASE) and gas chromatography-mass spectrometry. Different solvents were tested to extract activated charcoal tubes with the objective of replacing carbon disulfide, used in official methods, because of its highly toxic health and environmental effects. Extraction conditions, for example temperature and number of cycles, were investigated and optimized. The definitive extraction procedure selected was use of acetone at 150 °C and two consecutive extraction cycles at a pressure of 1,500 psi. Considering a sample volume of 0.005 Nm(3), corresponding to a sampling time of 8 h at a flow rate of 0.01 L min(-1), the method was validated over the concentration range 65-26,300 μg Nm(-3). The lowest limit of quantification was 6 μg Nm(-3), and recovery for the 93 % of analytes ranged from 65 to 102 %. For most of the compounds, relative standard deviations were less than 15 % for inter and intra-day precision. Uncertainty of measurement was also determined: the relative expanded uncertainty was always below 29.6 %, except for dichlorodifluoromethane. This work shows that use of friendlier solvent, for example acetone, coupled with use of ASE, can replace use of CS(2) for chemical removal of VOCs from activated charcoal. ASE has several advantages over traditional solvent-extraction methods, including shorter extraction time, minimum sample manipulation, high reproducibility, and less extraction discrimination. No loss of sensitivity occurs and there is also a salutary effect on bench workers' health and on the smell of laboratory air. PMID:22968683

  3. Rare earths: preparation of spectro chemically pure standards, study of their carbonates and synthesis of a new compound series - the peroxy carbonates; Terras-raras: obtencao de padroes espectroquimicos, estudo dos carbonatos e sintese dos peroxicarbonatos. Uma nova serie de compostos

    Energy Technology Data Exchange (ETDEWEB)

    Queiroz, Carlos Alberto da Silva

    1996-05-01

    In this work the following studies are concerned: I) preparation of lanthanum, cerium, praseodymium, neodymium and samarium oxides for use as spectro chemically pure standards; II) behavior of the rare earth (La, Ce, Pr, Nd, Sm) carbonates soluble in ammonium carbonate and mixture of ammonium carbonate/ammonium hydroxide, and III) synthesis and characterization of rare earth peroxy carbonates - a new series of compounds. Data for the synthesis and characterization of the rare earths peroxy carbonates described for the first time in this work are presented and discussed. With the aid of thermal analysis (TG-DTG) the thermal stability and the stoichiometric composition for new compounds were established and a mechanism of thermal decomposition was proposed. The peroxy carbonate was prepared by the addition of hydrogen peroxyde to the complexed soluble rare earths carbonates. These studies included also the determinations of active oxygen, the total rare earth oxide by gravimetry and complexometry and the C, H and N contents by microanalysis. The new compounds were also investigated by infrared spectroscopy. (author)

  4. Characterization of volatile organic compound adsorption on multiwall carbon nanotubes under different levels of relative humidity using linear solvation energy relationship.

    Science.gov (United States)

    Li, Mei-Syue; Wu, Siang Chen; Shih, Yang-Hsin

    2016-09-01

    Multiwall carbon nanotubes (MWCNTs) have been used as an adsorbent for evaluating the gas/solid partitioning of selected volatile organic compounds (VOCs). In this study, 15 VOCs were probed to determine their gas/solid partitioning coefficient (LogKd) using inverse gas chromatography at different relative humidity (RH) levels. Interactions between MWCNTs and VOCs were analyzed by regressing the observed LogKd with the linear solvation energy relationship (LSER). The results demonstrate that the MWCNT carbonyl and carboxyl groups provide high adsorption capacity for the VOCs (LogKd 3.72-5.24g/kg/g/L) because of the π-/n-electron pair interactions and hydrogen-bond acidity. The increasing RH gradually decreased the LogKd and shifted the interactions to dipolarity/polarizability, hydrogen-bond basicity, and cavity formation. The derived LSER equations provided adequate fits of LogKd, which is useful for VOC-removal processes and fate prediction of VOC contaminants by MWCNT adsorption in the environment. PMID:27152974

  5. Trace-chitosan-wrapped multi-walled carbon nanotubes as a new sorbent in dispersive micro solid-phase extraction to determine phenolic compounds.

    Science.gov (United States)

    Cao, Wan; Hu, Shuai-Shuai; Ye, Li-Hong; Cao, Jun; Xu, Jing-Jing; Pang, Xiao-Qing

    2015-04-17

    This report describes the use of trace-chitosan-wrapped multi-walled carbon nanotubes (CS-MWCNTs) as a sorbent material in dispersive micro solid-phase extraction (DMSPE), which was combined with ultra-high-performance liquid chromatography coupled with quadrupole time-of-flight tandem mass spectrometry to analyze phenolic compounds in chrysanthemum tea and a chrysanthemum beverage. In this study, for the first time, CS-MWCNTs were used as a sorbent for this microextraction mode. Moreover, the proposed method exhibits the advantages of simplicity, rapidity, small sample amount and ease of operation. Furthermore, all of the important parameters that affect the extraction efficiency, such as the sorbent, pH, extraction time and type of elution solvent, were investigated and optimized in the DMSPE. Under the optimized extraction condition, the limit of detection, which was calculated based on a signal-to-noise ratio of 3, was 0.22-16.19ngmL(-1). Satisfactory recovery values of 89-106% were obtained for the tested samples. The results show that the developed method was successfully applied to determine the content of chlorogenic acid and flavonoids in complex chrysanthemum samples. PMID:25748543

  6. Bifunctional quaternary ammonium compounds to inhibit biofilm growth and enhance performance for activated carbon air-cathode in microbial fuel cells

    Science.gov (United States)

    Li, Nan; Liu, Yinan; An, Jingkun; Feng, Cuijuan; Wang, Xin

    2014-12-01

    The slow diffusion of hydroxyl out of the catalyst layer as well as the biofouling on the surface of cathode are two problems affecting power for membrane-less air-cathode microbial fuel cells (MFCs). In order to solve both of them simultaneously, here we simply modify activated carbon air-cathode using a bifunctional quaternary ammonium compound (QAC) by forced evaporation. The maximum power density reaches 1041 ± 12 mW m-2 in an unbuffered medium (0.5 g L-1 NaCl), which is 17% higher than the control, probably due to the accelerated anion transport in the catalyst layer. After 2 months, the protein content reduced by a factor of 26 and the power density increases by 33%, indicating that the QAC modification can effectively inhibit the growth of cathodic biofilm and improve the stability of performance. The addition of NaOH and QAC epoxy have a negative effect on power production due to the clogging of pores in catalyst layer.

  7. Kinetics and thermodynamics of adsorption of ionizable aromatic compounds from aqueous solutions by as-prepared and oxidized multiwalled carbon nanotubes

    International Nuclear Information System (INIS)

    The adsorption of 1-naphthylamine, 1-naphthol and phenol on as-prepared and oxidized multiwalled carbon nanotubes (MWCNTs) has been investigated. The results illustrated that both as-prepared and oxidized MWCNTs showed high adsorption capacity for the three ionizable aromatic compounds (IACs) studied. Oxidation of MWCNTs increased the surface area and the pore volume, and introduced oxygen-containing functional groups to the surfaces of MWCNTs, which depressed the adsorption of IACs on MWCNTs. Both Langmuir and Freundlich models described the adsorption isotherms very well and the adsorption thermodynamic parameters (ΔGo, ΔHo and ΔSo) were measured. The adsorption for 1-naphthylamine, 1-naphthol and phenol is general spontaneous and thermodynamically favorable. The adsorption of phenol is an exothermic process, whereas the adsorption of 1-naphthylamine and 1-naphthol is an endothermic process. Results of this work are of great significance for the environmental application of MWCNTs for the removal of IACs from large volume of aqueous solutions.

  8. Improvement of visible light-induced photocatalytic performance by Cr-doped SrTiO3-carbon nitride intercalation compound (CNIC) composite

    Institute of Scientific and Technical Information of China (English)

    杨明; 金效齐

    2016-01-01

    Novel organic−inorganic composite photocatalyst offers new opportunities in the practical applications of photocatalysis. Novel visible light-induced Cr-doped SrTiO3–carbon nitride intercalation compound (CNIC) composite photocatalysts were synthesized. The composite photocatalyst was characterized by X-ray diffraction (XRD), field-emission scanning electron microscopy (FESEM), high-resolution transmission electron microscopy (HRTEM), Fourier transform infrared (FT-IR) spectroscopy, UV-vis diffuse reflection spectroscopy, photoluminescence (PL) spectroscopy, and BET surface area analyzer. The photocatalytic oxidation ability of the novel composite photocatalyst was evaluated using methyl orange (MO) as a target pollutant. The photocatalysts exhibited a significantly enhanced photocatalytic performance in degrading MO. For maximizing the photodegradation activity of the composite photocatalysts, the optimal CNIC content was determined. The improved photocatalytic activity of the as-prepared Cr-doped SrTiO3–CNIC composite photocatalyst may be attributed to the enhancement of photo-generated electron–hole separations at the interface.

  9. Highly porous CdO nanowires: preparation based on hydroxy- and carbonate-containing cadmium compound precursor nanowires, gas sensing and optical properties

    International Nuclear Information System (INIS)

    Highly porous cadmium oxide (CdO) nanowires have been prepared by calcining the hydroxy- and carbonate-containing cadmium compound precursor nanowires. The large-scale precursor nanowires were synthesized through a hydrothermal method. Scanning electron microscopy (SEM) and transmission electron microscopy (TEM) were employed to characterize and analyze the as-synthesized precursor nanowires as well as the calcined products. It was revealed that the wire-like morphology of the precursor was fundamentally retained during the process of calcination and the CdO nanowires obtained were polycrystalline with highly porous structures. In order to illustrate the formation mechanism of the porous structures, the morphology and composition evolutions of the precursor nanowires under different stages of the calcining process were further investigated via SEM, x-ray diffraction (XRD) and infrared (IR) absorbance spectroscopy. Gas sensing has been explored for the sensor device fabricated with highly porous CdO nanowires, which demonstrates that it has good response owing to its special structures and great selectivity to NOx. Furthermore, the UV-visible and photoluminescence spectra of highly porous CdO nanowires have also been investigated

  10. Carbon nanohoops and methods of making

    Energy Technology Data Exchange (ETDEWEB)

    Jasti, Ramesh; Bertozzi, Carolyn

    2015-03-24

    The present invention provides cycloparaphenylene compounds, their macrocyclic precursors, and methods for making the compounds. The cycloparaphenylene compounds can be used to prepare armchair carbon nanotubes.

  11. Carbon nanohoops and methods of making

    Energy Technology Data Exchange (ETDEWEB)

    Jasti, Ramesh; Bertozzi, Carolyn

    2015-10-20

    The present invention provides cycloparaphenylene compounds, their macrocyclic precursors, and methods for making the compounds. The cycloparaphenylene compounds can be used to prepare armchair carbon nanotubes.

  12. Characterization of Sulfur Compounds in MTBE

    OpenAIRE

    Mingqing Wu; Chunyan Chang; Tao Li; Jian Zhou; Liping Zhao

    2015-01-01

    A study is carried out on chemical constitution of sulfur compounds in MTBE and their formation mechanisms. These sulfur compounds are classified into three types: common sulfur compounds, newly formed sulfur compounds, and high boiling sulfur compounds. Common sulfur compounds which include mercaptans, low molecule sulfides and disulfides, are directly from C4, one of the stocks for production of MTBE. The newly formed sulfur compounds, with one sulfur atom and five or more total carbon atom...

  13. Nomenclature on an organic compound (I)

    International Nuclear Information System (INIS)

    This book is about nomenclature on an organic compound, which includes introduction with general principle on nomenclature on compounds it describes hydrocarbon like terpene hydrocarbon, basic heterocyclic organic compound including carbon, hydrogen, oxygen, nitrogen, halogen, sulfur, selenium and tellurium such as nomenclature system, halogen derivatives, alcohol and phenol derivatives, compound with sulfur, amino, nitroso and nitro compound, amino radical ion, azo and azoxy compound, compound including an atom group, hydrazine and derivatives.

  14. Land-use and Erosion Source Discrimination of Soil and Carbon Sources to the Logan and Albert Rivers in Australia using Compound Specific Isotope Analysis

    International Nuclear Information System (INIS)

    Full text: The compound specific isotope analysis (CSIA) technique has been used to identify the sources of soil erosion contributing sediment to the Logan-Albert catchment. Soil samples were collected in January 2010 and used to assess the ability of the CSIA technique to discriminate probable sources of soil erosion. Fatty acid and bulk carbon isotope signature (δ13C) were measured. This study has built on a previous sediment tracing study undertaken in 2008 using fallout radionuclides and major/minor element geochemistry. It was found that surface soils from forest, pasture and cultivated land uses are well discriminated using CSIA. Furthermore, sub-surface soil sources associated with channel bank erosion and exposed subsoils (gullies and hillslope scalds) occurring specifically in the mid-western Logan catchment could also be discriminated. The CSIA and bulk carbon δ13C data were used in the IsoSource mixing model to estimate the erosion sources of sediment collected during the January 2008 flood. The results of this analysis were compared with results obtained using other sediment tracers. For the lower Logan River, the CSIA tracing results are consistent with fallout and element geochemistry tracing, with channel bank erosion being confirmed as the major sediment source. However, the significant contribution to Logan River sediment of exposed subsoils originating on hillslopes and drainage lines from the mid-western region of the Logan catchment has also been confirmed by CSIA. This erosion source was not quantified by catchment modelling. In the Albert River catchment about 50% of soil comes from forest land use, although more than half of this soil comes from sub-surface sources. These results have demonstrated that the CSIA technique has the potential to significantly enhance the ability of CSIRO Land and Water sediment tracing studies to determine the extent that different land uses are contributing eroded soil to rivers, thus providing a check on

  15. Carbon sources in suspended particles and surface sediments from the Beaufort Sea revealed by molecular lipid biomarkers and compound-specific isotope analysis

    Directory of Open Access Journals (Sweden)

    I. Tolosa

    2013-03-01

    Full Text Available Molecular lipid biomarkers (hydrocarbons, alcohols, sterols and fatty acids and compound-specific isotope analysis of suspended particulate organic matter (SPM and surface sediments of the Mackenzie Shelf and slope (southeast Beaufort Sea, Arctic Ocean were studied in summer 2009. The concentrations of the molecular lipid markers, characteristic of known organic matter sources, were grouped and used as proxies to evaluate the relative importance of fresh algal, detrital algal, fossil, C3 terrestrial plants, bacterial and zooplankton material in the organic matter (OM of this area. Fossil and detrital algal contributions were the major fractions of the freshwater SPM from the Mackenzie River with ~34% each of the total molecular biomarkers. Fresh algal, C3 terrestrial, bacterial and zooplanktonic components represented much lower percentages, 17, 10, 4 and 80%, with a minor contribution of fossil and C3 terrestrial biomarkers. Characterization of the sediments revealed a major sink of refractory algal material mixed with some fresh algal material, fossil hydrocarbons and a small input of C3 terrestrial sources. In particular, the sediments from the shelf and at the mouth of the Amundsen Gulf presented the highest contribution of detrital algal material (60–75%, whereas those from the slope contained the highest proportion of fossil (40% and C3 terrestrial plant material (10%. Overall, considering that the detrital algal material is marine derived, autochthonous sources contributed more than allochthonous sources to the OM lipid pool. Using the ratio of an allochthonous biomarker (normalized to total organic carbon, TOC found in the sediments to those measured at the river mouth water, we estimated that the fraction of terrestrial material preserved in the sediments accounted for 30–40% of the total carbon in the inner shelf sediments, 17% in the outer shelf and Amundsen Gulf and up to 25% in the slope sediments. These estimates are low

  16. Compound-specific carbon isotope compositions of individual long-chain n-alkanes in severe Asian dust episodes in the North China coast in 2002

    Institute of Scientific and Technical Information of China (English)

    GUO Zhigang; LI Juyuan; FENG Jialiang; FANG Ming; YANG Zuosheng

    2006-01-01

    The molecular compositions and compound-specific carbon isotope compositions of individual long-chain n-alkanes of atmospheric aerosols collected during two severe Asian dust episodes in Qingdao in spring of 2002 were analyzed using gas chromatography/mass spectrometry (GC/MS) and gas chromatography/isotope ratio mass spectrometry (GC/IRMS). Typical plant wax n-alkanes (C29 and C31) had lowerδ13C values than those from anthropogenic (engine exhaust) sources (C21―C23). The average δ13C value of plant wax n-alkane C29 in non-dust episode periods was -30.5‰ (-30.3‰― -31.9‰), while -31.3‰ (-31.1‰―-31.5‰) in dust episode periods; for C31, it was -31.4‰ (-31.1‰―-33.0‰) in non-dust episode periods, and -31.7‰ (-31.3‰―-32.6‰) in dust episode periods. Plant wax in the dust episode samples was mainly from herbaceous plants via long-range transport, while local plant wax was mainly from deciduous plants and woody plants. In North China coast, 83.3% of the plant wax in the severe dust episode samples was from C3 plants while 80.0% for the non-dust samples, indicating that plant wax transported to the northwestern Pacific Ocean by airborne dust from East Asia was mainly from C3 plants. The results suggest that the molecular and molecular-isotopic compositions of individual long-chain n-alkanes can, as an effective indicator, identify the terrestrial organic components in the dust from East Asia and sediments in the northwest Pacific Ocean.

  17. Fabrication of new carbon paste electrodes based on gold nano-particles self-assembled to mercapto compounds as suitable ionophores for potentiometric determination of copper ions

    Directory of Open Access Journals (Sweden)

    Rasoul Pourtaghavi Talemi

    2013-12-01

    Full Text Available In the present study, we investigate the potentiometric behavior of Cu2+ carbon paste electrodes based on two mercapto compounds 2-ethylmino-5-mercapto-1,3,4-thiadiazole (EAMT and 2-acetylamino-5-mercapto-1,3,4-thiadiazole (AAMT self-assembled on gold nano-paricle (GNP as ionophore. Then, the obtained results from the modified electrodes are compared. The self-assembled ionophores exhibit a high selectivity for copper ion (Cu2+, in which the sulfur and nitrogen atoms in their structure play a significant role as the effective coordination donor site for the copper ion. Among these electrodes, the best performance was obtained with the sensor with a EAMT/graphite powder/paraffin oil weight ratio of 4.0/68/28 with 200 µL of GNP which exhibits the working concentration range of 1.6×10−9 to 6.3×10−2 M and a nernstian slope of 28.9±0.4 mVdecade−1 of copper(II activity. The detection limit of electrode was 2.9(±0.2×10−10M and potential response was pH ; in other words, it was independent across the range of 2.8–6.3. The proposed electrode presented very good selectivity and sensitivity towards the Cu2+ ions over a wide variety of cations including alkali, alkaline earth, transition and heavy metal ions. Moreover, the proposed electrode was successfully applied as an indicator electrode in the potentiometric titration of Cu(II ions with EDTA and also the potentiometric determination of copper ions in spiked water samples.

  18. A novel needle trap device with single wall carbon nanotubes sol-gel sorbent packed for sampling and analysis of volatile organohalogen compounds in air.

    Science.gov (United States)

    Heidari, Mahmoud; Bahrami, Abdolrahman; Ghiasvand, Ali Reza; Shahna, Farshid Ghorbani; Soltanian, Ali Reza

    2012-11-15

    This paper describes a new approach that combines needle trap devices (NTDs) with a newly synthesized silanated nano material as sorbent for sampling and analysis of HVOCs in air. The sol-gel technique was used for preparation of the single wall carbon nanotube (SWCNT)/silica composite as sorbent, packed inside a 21-gauge NTD. Application of this method as an exhaustive sampler device was investigated under different laboratory conditions in this study. Predetermined concentrations of each analyte were prepared in a home-made standard chamber, and the effects of experimental parameters, such as temperature, humidity, sampling air flow rate, breakthrough volume and storage time on NTD, and the sorbent performance were investigated. The proposed NTD was used in two different modes and two different injection methods, and an NTD with a side hole, a narrow neck glass liner and syringe pump assisted injection of carrier gas were applied. The NTD packed with SWCNTs/silica composite was compared to the NTD packed with PDMS and also SPME with CAR/PDMS. For four compounds, LOD was 0.001-0.01 ng mL(-1), LOQ was 0.007-0.03 ng mL(-1), and the relative standard division for repeatability of method was 2.5-6.7%. The results show that the incorporation of NTD and SWCNTs/silica composite is a reliable and effective approach for the sampling and analysis of HVOCs in air. Coupling this system to GC-MS make it more sensitive and powerful technique. PMID:23158328

  19. The Bark-Beetle-Associated Fungus, Endoconidiophora polonica, Utilizes the Phenolic Defense Compounds of Its Host as a Carbon Source1[OPEN

    Science.gov (United States)

    Wadke, Namita; Kandasamy, Dineshkumar; Vogel, Heiko; Wingfield, Brenda D.; Paetz, Christian

    2016-01-01

    Norway spruce (Picea abies) is periodically attacked by the bark beetle Ips typographus and its fungal associate, Endoconidiophora polonica, whose infection is thought to be required for successful beetle attack. Norway spruce produces terpenoid resins and phenolics in response to fungal and bark beetle invasion. However, how the fungal associate copes with these chemical defenses is still unclear. In this study, we investigated changes in the phenolic content of Norway spruce bark upon E. polonica infection and the biochemical factors mediating these changes. Although genes encoding the rate-limiting enzymes in Norway spruce stilbene and flavonoid biosynthesis were actively transcribed during fungal infection, there was a significant time-dependent decline of the corresponding metabolites in fungal lesions. In vitro feeding experiments with pure phenolics revealed that E. polonica transforms both stilbenes and flavonoids to muconoid-type ring-cleavage products, which are likely the first steps in the degradation of spruce defenses to substrates that can enter the tricarboxylic acid cycle. Four genes were identified in E. polonica that encode catechol dioxygenases carrying out these reactions. These enzymes catalyze the cleavage of phenolic rings with a vicinal dihydroxyl group to muconoid products accepting a wide range of Norway spruce-produced phenolics as substrates. The expression of these genes and E. polonica utilization of the most abundant spruce phenolics as carbon sources both correlated positively with fungal virulence in several strains. Thus, the pathways for the degradation of phenolic compounds in E. polonica, initiated by catechol dioxygenase action, are important to the infection, growth, and survival of this bark beetle-vectored fungus and may play a major role in the ability of I. typographus to colonize spruce trees. PMID:27208235

  20. Influence of mass recovery on the performance of a heat pipe type ammonia sorption refrigeration system using CaCl2/activated carbon as compound adsorbent

    International Nuclear Information System (INIS)

    The performance analyses of a sorption refrigeration system with different mass recovery processes are presented, in which compound adsorbent of CaCl2 and activated carbon is used to improve the mass and heat transfer performances of sorption bed. The heating, cooling and heat recovery processes between two sorption beds were performed by multifunction heat pipes without additional power consumption. The experimental Clapeyron diagrams showed that the cycles with mass recovery (MR), with heat and mass recoveries (HMR), and with mass and heat recoveries (MHR), have better thermodynamic performances when compared with the sorption cycle without mass recovery (MR0). The implementary order of mass recovery and heat recovery has strong influence on the efficacy of mass recovery while it has little influence on the efficacy of heat recovery. In sorption cycles with HMR and with MHR, the hot beds can be pre-cooled and cold beds can be pre-heated effectively during the switching process, and heat consumption from external heat source during desorption phase is thereby reduced. Mass recovery can enlarge cycled refrigerant mass due to the transfer of refrigerant gas between two sorption beds during mass recovery process. In comparison with sorption cycle with MR0, sorption cycles with MR, with HMR, and with MHR can generally improve the coefficient of performance (COP) and specific cooling power (SCP) by more than 20% and 16%, respectively. Especially, sorption cycle with MHR has the highest performance among different mass recovery processes due to the fact that MHR has the advantages of MR and HMR, and it can improve the COP by 46.7% when compared with the cycle with MR0

  1. [11C]Carbon Monoxide in Palladium- / Selenium-Promoted Carbonylation Reactions : Synthesis of 11C-Imides, Hydrazides, Amides, Carboxylic Acids, Carboxylic Esters, Carbothioates, Ketones and Carbamoyl Compounds

    OpenAIRE

    Karimi, Farhad

    2002-01-01

    [11C]Carbon monoxide in low concentrations has been used in palladium- or seleniummediated carbonylation reactions such as the synthesis of 11C-imides, hydrazides, amides, carboxylic acids, esters, carbothioates, ketones and carbamoyl compounds. In these reactions aryl iodides have been used in most cases. However, less reactive aryl triflate, chloride and bromides were activated using tetrabutylammonium iodide. The reactivities of nucleophiles may have influence on the radiochemical yield of...

  2. Nomenclature on an organic compound (II)

    International Nuclear Information System (INIS)

    This book deals with nomenclature on an organic compound except carbon, hydrogen, oxygen, nitrogen, halogen, sulfur, selenium and tellurium. It mentions introduction, nomenclature system, coordination compound, an organo-metallic compound, homogeneous chains and rings with regular form of heteroatoms, organic compound including arsenic, phosphorus and bismuth, stereochemistry, nomenclature of compound related a natural substance, modified compound in to an isotope. The last chapter has recommendation on general principle and instruction for nomenclature.

  3. Comparison of Vegetation Change Inferred From Palynology and Compound-Specific Carbon Isotopes of Lipid Biomarkers in the Maya Lowlands of Peten, Guatemala

    Science.gov (United States)

    Newell, S. D.; Hodell, D. A.; Curtis, J. H.; Brenner, M.; Venz-Curtis, K.

    2005-12-01

    The Petén region of northern Guatemala has been occupied by humans for more than 3000 years. Expansion of the Maya civilization during the Preclassic (~1000 BC to AD 250) and Classic (AD 250 to AD 900) Periods was accompanied by increasing deforestation of Petén watersheds and accelerated rates of soil erosion. Palynological data from Petén lake cores illustrate the near elimination of high forest taxa and prevalence of disturbance taxa (grasses, weeds) during the height of Classic Maya occupation (~AD 500 to AD 800). After flourishing during the Classic Period between AD 250 and 800, Maya population densities declined significantly in the Petén, thereby curtailing human pressures on the landscape. This cycle of population expansion and decline in the Petén provides a natural historical experiment that has been used to study the response of tropical vegetation to long-term changes in land-use by humans. We measured the carbon isotopic composition of long-chain n-alkanes of leaf waxes in two cores from Lakes Sacnab and Salpetén in the Petén Lake District of the southern Maya Lowlands. The carbon isotopic composition of leaf waxes has been shown to be a reliable indicator of the relative proportion of C3 to C4 biomass in a watershed. Biomarker results were compared directly to a pollen profile from Lake Salpetén. Although the general pattern of increased C4 abundance inferred from δ13C of long-chain n-alkanes and increased disturbance taxa from pollen studies agree during the period of Maya occupation, the two proxies differ in detail suggesting they are recording different characteristics of watershed vegetation. For example, the highest long-chain δ13C values (representing greatest C4 biomass) occurred during early settlement of the basins in the early to middle Preclassic Period (1300 to 500 BC) when Maya population densities were relatively low. This period also corresponded to the time of greatest erosion rates in the Salpetén basin (Anselmetti et al

  4. Hydrological and Vegetation Shifts in the Equatorial Sulawesi since the Last Glacial Maximum: Perspectives from Hydrogen and Carbon Isotopes of Terrestrial Leaf Wax Compounds

    Science.gov (United States)

    Wicaksono, Satrio; Russell, James; Holbourn, Ann; Kuhnt, Wolfgang

    2014-05-01

    Maritime Continent hydrological cycle is sensitive to Northern Hemisphere high-latitude climate events. Despite the lowering of global temperature during both the LGM and YD, the contrasting precipitation signals between the two events over Sulawesi also suggest that different climatic forcing and/or propagation mechanisms might have operated at different time scales. In addition, we will measure carbon isotopes of terrestrial leaf wax compounds (δ13Cwax) to investigate changes in local terrestrial vegetation assemblages and, by inference, the climate in which they grew. Covariation between our δDwax and δ13Cwax records may corroborate our interpretation of δDwax as a robust tropical paleoprecipitation proxy.

  5. Enhanced corrosion resistance of carbon steel in normal sulfuric acid medium by some macrocyclic polyether compounds containing a 1,3,4-thiadiazole moiety: AC impedance and computational studies

    Energy Technology Data Exchange (ETDEWEB)

    Bentiss, F. [Laboratoire de Chimie de Coordination et d' Analytique, Faculte des Sciences, Universite Chouaib Doukkali, B.P. 20, M-24000 El Jadida (Morocco)], E-mail: fbentiss@enscl.fr; Lebrini, M. [Unite de Catalyse et de Chimie du Solide, UMR-CNRS 8181, ENSCL, BP. 90108, F-59652 Villeneuve d' Ascq Cedex (France); Vezin, H. [Laboratoire de Chimie Organique et Macromoleculaire, UMR-CNRS 8009, USTL Bat C4, F-59655 Villeneuve d' Ascq Cedex (France); Chai, F. [Groupe de Recherche sur les biomateriaux, Laboratoire de Biophysique, UPRES EA 1049, Faculte de Medecine, F-59045 Lille Cedex (France); Traisnel, M.; Lagrene, M. [Laboratoire des Procedes d' Elaboration des Revetements Fonctionnels, PERF UMR-CNRS 8008, ENSCL, B.P. 90108, F-59652 Villeneuve d' Ascq Cedex (France)

    2009-09-15

    We report here the use of macrocyclic polyether compounds containing a 1,3,4-thiadiazole moiety (n-MCTH) in the corrosion inhibition of C38 carbon steel in 0.5 M H{sub 2}SO{sub 4} acid medium. The aim of this work is devoted to study the inhibition characteristics of these compounds for acid corrosion of C38 steel using electrochemical impedance spectroscopy (EIS). Data obtained from EIS show a frequency distribution and therefore a modeling element with frequency dispersion behaviour, a constant phase element (CPE) has been used. The experimental results obtained revealed that these compounds inhibited the steel corrosion in acid solution and the protection efficiency increased with increasing inhibitors concentration. The difference in their inhibitive action can be explained on the basis of the number of oxygen atoms present in the polyether ring which contribute to the chemisorption strength through the donor acceptor bond between the non bonding electron pair and the vacant orbital of metal surface. Adsorption of n-MCTH was found to follow the Langmuir's adsorption isotherm. The thermodynamic functions of adsorption process were calculated and the interpretation of the results is given. These results are complemented with quantum chemical study in order to provide an explanation of the differences between the probed inhibitors. Correlation between the inhibition efficiency and the structure of these compounds are presented.

  6. Fe organoiron compounds. Pt. B11

    International Nuclear Information System (INIS)

    The chapter of compounds with ligands bonded by five carbon atoms deals with one 5L ligand, one 5L ligands and additional 1L ligands. In this chapter, there are different type compounds or complexes with iron containing carbonyl nitroxyl. The chapter of compounds with two CO ligands present the organoiron compounds with halide, where we find chemical properties, physical properties, analysis, adducts formation with halogen. In the last chapters, different compound with oxygen, nitrogen and their mechanism is discussed. (AB)

  7. Investigations on organogermanium compounds XII. Reactions of trialkylgermylalkalimetal compounds in hexamethylphosphoric triamide (HMPT) with some inorganic and organic compounds

    NARCIS (Netherlands)

    Bulten, E.J.; Noltes, J.G.

    1971-01-01

    Trialkylgermyl alkali metal compounds in HMPT have been found to be highly reactive nucleophiles. Reactions with some inorganic and organic compounds, such as oxygen, carbon dioxide, inorganic and orgaanic halides, aldehydes, ketones, epoxides and lactones are described. Several new carbon-functiona

  8. Applications of Technology of Compound Lining of Semi—gr aphitized Self—baking Carbon Block Ceramic Brickwork in Large—sized Blast Furnaces

    Institute of Scientific and Technical Information of China (English)

    HAOYung-zhong; CHENQian-wan

    1994-01-01

    Based on the analyses of the lining technologies of the hot press formed carbon brick iu U.S.A., of the ce-ramic cup in France and of the creative self-baking car-bon brick in China,the technology of semi-graphitized car-bon block-ceramic brickwork has been studied and developed ,and has successfully ben used in No.7 blast furnace (2580m3) at Anshan Irom and Steel Company and in No.3 blast furnace (1200m3) at Taiyuan Iron and Steel Company,This paper puts fourward a feasible scheme for realization of long service lives of the bootms and the hearths of large-sized blast furaces in China.

  9. Phenolic Molding Compounds

    Science.gov (United States)

    Koizumi, Koji; Charles, Ted; de Keyser, Hendrik

    Phenolic Molding Compounds continue to exhibit well balanced properties such as heat resistance, chemical resistance, dimensional stability, and creep resistance. They are widely applied in electrical, appliance, small engine, commutator, and automotive applications. As the focus of the automotive industry is weight reduction for greater fuel efficiency, phenolic molding compounds become appealing alternatives to metals. Current market volumes and trends, formulation components and its impact on properties, and a review of common manufacturing methods are presented. Molding processes as well as unique advanced techniques such as high temperature molding, live sprue, and injection/compression technique provide additional benefits in improving the performance characterisitics of phenolic molding compounds. Of special interest are descriptions of some of the latest innovations in automotive components, such as the phenolic intake manifold and valve block for dual clutch transmissions. The chapter also characterizes the most recent developments in new materials, including long glass phenolic molding compounds and carbon fiber reinforced phenolic molding compounds exhibiting a 10-20-fold increase in Charpy impact strength when compared to short fiber filled materials. The role of fatigue testing and fatigue fracture behavior presents some insight into long-term reliability and durability of glass-filled phenolic molding compounds. A section on new technology outlines the important factors to consider in modeling phenolic parts by finite element analysis and flow simulation.

  10. Sorption of tannin and related phenolic compounds and effects on extraction of soluble-N in soil amended with several carbon sources

    Science.gov (United States)

    Some tannins, phenolic substances produced by plants, sorb to soil and reduce the extraction of soluble-N and thus could influence soil organic matter (SOM) and nutrient cycling. However, we know little about how these compounds interact with organic amendments in soil. Surface soil (0-5cm) from p...

  11. Organic Compounds in Carbonaceous Meteorites

    Science.gov (United States)

    Cooper, Grorge

    2001-01-01

    Carbonaceous meteorites are relatively enriched in soluble organic compounds. To date, these compounds provide the only record available to study a range of organic chemical processes in the early Solar System chemistry. The Murchison meteorite is the best-characterized carbonaceous meteorite with respect to organic chemistry. The study of its organic compounds has related principally to aqueous meteorite parent body chemistry and compounds of potential importance for the origin of life. Among the classes of organic compounds found in Murchison are amino acids, amides, carboxylic acids, hydroxy acids, sulfonic acids, phosphonic acids, purines and pyrimidines (Table 1). Compounds such as these were quite likely delivered to the early Earth in asteroids and comets. Until now, polyhydroxylated compounds (polyols), including sugars (polyhydroxy aldehydes or ketones), sugar alcohols, sugar acids, etc., had not been identified in Murchison. Ribose and deoxyribose, five-carbon sugars, are central to the role of contemporary nucleic acids, DNA and RNA. Glycerol, a three-carbon sugar alcohol, is a constituent of all known biological membranes. Due to the relative lability of sugars, some researchers have questioned the lifetime of sugars under the presumed conditions on the early Earth and postulated other (more stable) compounds as constituents of the first replicating molecules. The identification of potential sources and/or formation mechanisms of pre-biotic polyols would add to the understanding of what organic compounds were available, and for what length of time, on the ancient Earth.

  12. A Statistical Estimation Approach for Quantitative Concentrations of Compounds Lacking Authentic Standards/Surrogates Based on Linear Correlations between Directly Measured Detector Responses and Carbon Number of Different Functional Groups

    Directory of Open Access Journals (Sweden)

    Yong-Hyun Kim

    2013-01-01

    Full Text Available A statistical approach was investigated to estimate the concentration of compounds lacking authentic standards/surrogates (CLASS. As a means to assess the reliability of this approach, the response factor (RF of CLASS is derived by predictive equations based on a linear regression (LR analysis between the actual RF (by external calibration of 18 reference volatile organic compounds (VOCs consisting of six original functional groups and their physicochemical parameters ((1 carbon number (CN, (2 molecular weight (MW, and (3 boiling point (BP. If the experimental bias is estimated in terms of percent difference (PD between the actual and projected RF, the least bias for 18 VOCs is found from CN (17.9±19.0%. In contrast, the PD values against MW and BP are 40.6% and 81.5%, respectively. Predictive equations were hence derived via an LR analysis between the actual RF and CN for 29 groups: (1 one group consisting of all 18 reference VOCs, (2 three out of six original functional groups, and (3 25 groups formed randomly from the six functional groups. The applicability of this method was tested by fitting these 29 equations into each of the six original functional groups. According to this approach, the mean PD for 18 compounds dropped as low as 5.60±5.63%. This approach can thus be used as a practical tool to assess the quantitative data for CLASS.

  13. Insulating and sheathing materials of electric and optical cables: common test methods part 4-1: methods specific to polyethylene and polypropylene compounds – resistance to environmental stress cracking – measurement of the melt flow index – carbon black and/or mineral filler content measurement in polyethylene by direct combustion – measurement of carbon black content by thermogravimetric analysis (TGA) – assessment of carbon black dispersion in polyethylene using a microscope

    CERN Document Server

    International Electrotechnical Commission. Geneva

    2004-01-01

    Specifies the test methods to be used for testing polymeric insulating and sheathing materials of electric cables for power distribution and telecommunications including cables used on ships. Gives the methods for measurements of the resistance to environmental stress cracking, for wrapping test after thermal ageing in air, for measurement of melt flow index and for measurement of carbon black and/or mineral filler content, which apply to PE and PP coumpounds, including cellular compounds and foam skin for insulation.

  14. Morphology, mechanical, cross-linking, thermal, and tribological properties of nitrile and hydrogenated nitrile rubber/multi-walled carbon nanotubes composites prepared by melt compounding: The effect of acrylonitrile content and hydrogenation

    International Nuclear Information System (INIS)

    The purpose of this work was to prepare nanocomposites by mixing multi-walled carbon nanotubes (MWCNT) with nitrile and hydrogenated nitrile elastomers (NBR and HNBR). Utilization of transmission electronic microscopy (TEM), scanning electron microscopy (SEM), and small- and wide-angle X-ray scattering techniques (SAXS and WAXS) for advanced morphology observation of conducting filler-reinforced nitrile and hydrogenated nitrile rubber composites is reported. Principal results were increases in hardness (maximally 97 Shore, type A), elastic modulus (maximally 981 MPa), tensile strength (maximally 27.7 MPa), elongation at break (maximally 216%), cross-link density (maximally 7.94 x 1028 m-3), density (maximally 1.16 g cm-3), and tear strength (11.2 kN m-1), which were clearly visible at particular acrylonitrile contents both for unhydrogenated and hydrogenated polymers due to enhanced distribution of carbon nanotubes (CNT) and their aggregated particles in the applied rubber matrix. Conclusion was that multi-walled carbon nanotubes improved the performance of nitrile and hydrogenated nitrile rubber nanocomposites prepared by melt compounding.

  15. Elevated Carbon Dioxide Increases Contents of Flavonoids and Phenolic Compounds, and Antioxidant Activities in Malaysian Young Ginger (Zingiber officinale Roscoe. Varieties

    Directory of Open Access Journals (Sweden)

    Asmah Rahmat

    2010-11-01

    Full Text Available Zingiber officinale Roscoe. (Family Zingiberaceae is well known in Asia. The plant is widely cultivated in village gardens in the tropics for its medicinal properties and as a marketable spice in Malaysia. Ginger varieties are rich in physiologically active phenolics and flavonoids with a range of pharmacological activities. Experiments were conducted to determine the feasibility of increasing levels of flavonoids (quercetin, rutin, catechin, epicatechin, kaempferol, naringenin, fisetin and morin and phenolic acid (gallic acid, vanillic acid, ferulic acid, tannic acid, cinnamic acid and salicylic acid, and antioxidant activities in different parts of Malaysian young ginger varieties (Halia Bentong and Halia Bara with CO2 enrichment in a controlled environment system. Both varieties showed an increase in phenolic compounds and flavonoids in response to CO2 enrichment from 400 to 800 µmol mol-1 CO2. These increases were greater in rhizomes compared to leaves. High performance liquid chromatography (HPLC results showed that quercetin and gallic acid were the most abundant flavonoid and phenolic acid in Malaysian young ginger varieties. Under elevated CO2 conditions, kaempferol and fisetin were among the flavonoid compounds, and gallic acid and vanillic acid were among the phenolic compounds whose levels increased in both varieties. As CO2 concentration was increased from 400 to 800 µmol mol-1, free radical scavenging power (DPPH increased about 30% in Halia Bentong and 21.4% in Halia Bara; and the rhizomes exhibited more enhanced free radical scavenging power, with 44.9% in Halia Bentong and 46.2% in Halia Bara. Leaves of both varieties also displayed good levels of flavonoid compounds and antioxidant activities. These results indicate that the yield and pharmaceutical quality of Malaysian young ginger varieties can be enhanced by controlled environment production and CO2 enrichment.

  16. Extraction of phenolic compounds from elder berry and different grape marc varieties using organic solvents and/or supercritical carbon dioxide

    OpenAIRE

    Vatai, Tünde; Škerget, Mojca; KNEZ, ŽELJKO

    2012-01-01

    Optimal operating conditions for the extraction of phenolic compounds from grape marc and elder berry have been investigated. The aim was to obtain extracts with high anthocyanin content, which show stability during storage and would be potentially interesting for commercial applications as natural colorants. For this purpose three varieties of grape marc, native to Slovenia (Refošk, Merlot and Cabernet), were studied. The results were compared with the extraction of elder berry, which is kno...

  17. Acetalization of carbonyl compounds with 2,2,4-trimethyl-1,3-pentanedio catalyzed by novel carbon based solid acid catalyst

    Institute of Scientific and Technical Information of China (English)

    Ling Liu; Yuechang Zhao; Shan Gan; Xuezheng Liang; Jianguo Yang; Mingyuan He

    2008-01-01

    The synthesis of 2, 4-diisopropyl-5,5-dimethyl-1,3-dioxane through the acetalization of isobutyraldehyde with 2, 2,4-trimethyl-1,3-pentanediol (TMPD) catalyzed by the novel carbon based acid was first carried out. High conversion (≥98%) and specific selectivity were obtained using the novel carbon based acid, which kept high activity after it was reused 5 times.Moreover, the catalyst could be used to catalyze the acetalization and ketalization of different aldehydes and ketones with superior yield. The yield of several products was over 90%. The novel heterogeneous catalyst has the distinct advantages of high activity, strikingly simple workup procedure, non-pollution, and reusability, which will contribute to the success of the green process greatly.

  18. Compósitos de Borracha Natural com Compostos Condutivos à Base de Negro de Fumo e Polímero Condutor Natural Rubber Composites with Conductive Compounds based on Carbon Black and Conducting Polymers

    Directory of Open Access Journals (Sweden)

    Marinalva A. dos Santos

    2001-09-01

    Full Text Available Neste trabalho foram desenvolvidos compósitos condutores elétricos de borracha natural contendo negro de fumo e compostos condutivos baseados em polímeros condutores (Eenomer®. Os compósitos foram processados a quente num reômetro de torque HAAKE e moldados por prensagem. Foram obtidas placas homogêneas, flexíveis e com ótimo acabamento superficial. Os compósitos foram analisados pelas medidas de torque no processamento, medidas de condutividade elétrica, análise termogravimétrica (TGA, calorimetria diferencial de varredura (DSC e ensaios de tração. Estes compósitos apresentaram valores de condutividade elétrica entre 10-7 a 10-1 S/cm, dependendo do tipo de negro de fumo ou composto condutivo utilizado e da quantidade destes no compósito. A análise térmica demonstrou que os compósitos são termicamente estáveis até cerca de 300°C. Os compostos condutivos atuam como reforço para a borracha natural melhorando suas propriedades mecânicas sem perder significativamente sua flexibilidade.In this work, electrically conducting composites of natural rubber with carbon black and natural rubber with conductive compounds containing electrically conducting polymers (Eenomer® were developed. The composites were processed in a torque reometer HAAKE and then hot pressed. Homogeneous and flexible plates were obtained with excellent surface finish. The composites were analysed by the torque measurement during processing, electrical conductivity, thermogravimetric analysis (TGA, differential scanning calorimetric (DSC and mechanical analysis. Conductivity in the order of 10-7 to 10-1 S/cm were achieved, depending on the type of carbon black or conductive compound used and their content in the composite. Thermal analysis demonstrated that the compounds are thermally stable until 300°C. The conductive compounds act as reinforcements in the natural rubber matrix, improving its mechanical properties without significant loss on its

  19. Design and Synthesis of 11C-Labelled Compound Libraries for the Molecular Imaging of EGFr, VEGFr-2, AT1 and AT2 Receptors: Transition-Metal Mediated Carbonylations Using [11C]Carbon Monoxide

    International Nuclear Information System (INIS)

    This work deals with radiochemistry and new approaches to develop novel PET tracers labelled with the radionuclide 11C. Two methods for the synthesis of 11C-labelled acrylamides have been explored. First, [1-11C]-acrylic acid was obtained from a palladium(0)-mediated 11C-carboxylation of acetylene with [11C]carbon monoxide; this could be converted to the corresponding acyl chloride and then combined with benzylamine to form N-benzyl[carbonyl-11C]acrylamide. In the second method, the palladium(0)-mediated carbonylation of vinyl halides with [11C]carbon monoxide was explored. This latter method, yielded labelled acrylamides in a single step with retention of configuration at the C=C double bond, and required less amine compared to the acetylene method. The vinyl halide method was used to synthesize a library of 11C-labelled EGFr-inhibitors in 7-61% decay corrected radiochemical yield via a combinatorial approach. The compounds were designed to target either the active or the inactive form of EGFr, following computational docking studies. The rhodium(I)-mediated carbonylative cross-coupling of an azide and an amine was shown to be a very general reaction and was used to synthesize a library of dual VEGFr-2/PDGFrβ inhibitors that were 11C-labelled at the urea position in 38-78% dc rcy. The angiotensin II AT1 receptor antagonist eprosartan was 11C-labelled at one of the carboxyl groups in one step using a palladium(0)-mediated carboxylation. Autoradiography shows specific binding in rat kidney, lung and adrenal cortex, and organ distribution shows a high accumulation in the intestines, kidneys and liver. Specific binding in frozen sections of human adrenal incidentalomas warrants further investigations of this tracer. Three angiotensin II AT2 ligands were 11C-labelled at the amide group in a palladium(0)-mediated aminocarbonylation in 16-36% dc rcy. One of the compounds was evaluated using in vitro using autoradiography, and in vivo using organ distribution and animal

  20. Effects of carbon on Pr0.15Tb0.30Dy0.55Fe1.85 compound

    Institute of Scientific and Technical Information of China (English)

    LIU Heyan; LI Yangxian; YU Xiao; LI Songtao; MENG Xiangxi; XU Xuewen

    2006-01-01

    The structure, Curie temperature and magnetostriction of Pr0.15Tb0.30Dy0.55Fe1.85Cx (x=0-0.1) compounds were investigated by X-ray diffraction, a vibrating sample magnetometer and a standard strain technique.All the samples show entirely MgCu2-type Laves phase structure.The lattice parameter and Curie temperature increase with C content increasing.The magnetostriction at high magnetic field shows maximum value at x=0.05.

  1. Multipurpose Compound

    Science.gov (United States)

    1983-01-01

    Specially formulated derivatives of an unusual basic compound known as Alcide may be the answer to effective treatment and prevention of the disease bovine mastitis, a bacterial inflammation of a cow's mammary gland that results in loss of milk production and in extreme cases, death. Manufactured by Alcide Corporation the Alcide compound has killed all tested bacteria, virus and fungi, shortly after contact, with minimal toxic effects on humans or animals. Alcide Corporation credits the existence of the mastitis treatment/prevention products to assistance provided the company by NERAC, Inc.

  2. Phenyl-functionalized magnetic palm-based powdered activated carbon for the effective removal of selected pharmaceutical and endocrine-disruptive compounds.

    Science.gov (United States)

    Wong, Kien Tiek; Yoon, Yeomin; Snyder, Shane A; Jang, Min

    2016-06-01

    Triethoxyphenylsilane (TEPS)-functionalized magnetic palm-based powdered activated carbon (MPPAC-TEPS) was prepared and characterized using various spectroscopic methods, and then tested for the removal of bisphenol A, carbamazepine, ibuprofen and clofibric acid. Magnetite film on MPPAC-TEPS was homogeneously coated on the outer surface of palm-based powdered activated carbon (PPAC) through a hydrothermal co-precipitation technique. Followed by silanization of phenyl-functionalized organosilane on MPPAC's magnetic film. As results, micro/mesopore surface area and volume increased without significant pore clogging and iron (Fe) dissolution under the acidic conditions was greatly decreased. The unique structural and chemical features of MPPAC-TEPS were found to be the main reasons for the enhanced adsorption rates and removal capacities of POPs. The presence of electrolytes and different pH values greatly affected the sorption efficiencies. The dominant sorption mechanism of POPs by MPPAC-TEPS was determined to be π-π interaction (physisorption), based on thermodynamic (ΔG°) and differential scanning calorimetry (DSC). Thermal regeneration at a low temperature (350 °C) was an effective method to desorb the retained POPs and enabled to reactivate MPPAC-TEPS with sustained sorption rates and capacities, whereas PPAC was largely exhausted. As a new type of sorbent for POPs, MPPAC-TEPS has operational advantages, such as magnetic separation and stable regeneration. PMID:26963238

  3. 乙腈溶剂中单壁碳纳米管与常见有机化合物的相互作用%Interactions between single-walled carbon nanotubes and common organic compounds in acetoaitrile

    Institute of Scientific and Technical Information of China (English)

    褚莹倩; 李雪花; 杨先海; 张晓琳; 陈景文

    2013-01-01

    Single-walled carbon nanotubes ( SWCNTs) , used as the stationary phase materials, were packed into the HPLC column by the downward slurry method. Retention factors of 18 common organic compounds in acetonitrile phase on SWCNTs column were measured and used to investigate the interaction between SWCNTs and organic compounds. The results show that the interactions between SWCNTs and organic compounds in acetonitrile phase are related to the number and types of functional groups and the number of hetero-atoms. The interactions between SWCNTs and organic compounds were characterized quantitatively using the linear solvation energy relationships (LSER). The obtained LSER model has a goodness of fit (R2 =0. 844) and robustness (Q2LOO =0. 768). The results demonstrate that the interaction with π-/n- electrons and cavity/dispersion interactions are the main factors that influence the interactions between SWCNTs and organic compounds.%以单壁碳纳米管( SWCNTs)为固定相,采用高压匀浆法,制备HPLC色谱柱.测定乙腈相中18种有机化合物在SWCNTs色谱柱上的保留因子,研究SWCNTs与化合物的相互作用.结果表明,有机化合物取代基的种类和个数、杂原子的个数影响乙腈相中有机化合物与SWCNTs的相互作用.采用线性溶解能关系( LSER)定量表征SWCNTs与有机化合物的相互作用,所构建的LSER模型具有较强的拟合能力(R2=0.844)和稳健性(Q2LOO =0.768),发现π-/n-电子对作用和空穴/弥散作用是控制SWCNTs与有机化合物相互作用的主要因素.

  4. Efeito da presença e concentração de compostos carbonílicos na qualidade de vinhos Effects of carbonylic compound presence and concentration on wine quality

    Directory of Open Access Journals (Sweden)

    Luciana C. de Azevêdo

    2007-01-01

    Full Text Available Studies on identification of compounds that make up the aroma and flavor in wines involve research evaluating mainly the influence of terpenes, esters, lactones and alcohols upon these sensory characteristics. However, carbonylic compounds (CC play an important role concerning the substances that impact aroma to these drinks. Their origin is reported to be linked to the grape's chemical composition, must fermentation or micro-oxidation occurring during storage in barrels. Some CCs, like E-ionone, E-damascenone, siryngaldehyde, can contribute a pleasant aroma and improve the wine quality whereas others are responsible for unpleasant characteristics (acetaldehyde, furfural, 5-hydroxy-methyl furfural, diacetil, E-non-2-enal, etc. A fraction of CCs present is associated with bisulfite ions in the form of hydroxyalkylsulfonic acids. Some of them are stable and play an important role in determining wine quality. The reaction involving the formation of this aduct commonly occurs with CCs of low molar mass, such as formaldehyde and acetaldehyde. The reaction involving CCs with more than three carbon atoms demands further studies.

  5. Preparation of a novel ionic hybrid stationary phase by non-covalent functionalization of single-walled carbon nanotubes with amino-derivatized silica gel for fast HPLC separation of aromatic compounds.

    Science.gov (United States)

    Aral, Hayriye; Çelik, K Serdar; Aral, Tarık; Topal, Giray

    2016-03-01

    Single-walled carbon nanotubes (SWCNTs) were immobilized on spherical silica gel with a 4-μm average particle size and a 60-Å average pore size. The amino-derivatized silica gel was non-covalently coated with carboxylated SWCNTs to preserve the structure of the nanotubes and their physico-chemical properties. The novel ionic hybrid stationary phase was characterized by scanning electron microscopy (SEM), infra-red (IR) spectroscopy and elemental analysis, and then, it was used to fill an empty 150×4.6mm(2) high-performance liquid chromatography (HPLC) column. Chromatographic parameters, such as the theoretical plate number, retention factor and peak asymmetry factor, and analytical parameters, such as the limit of detection (LOD), limit of quantification (LOQ), linear range, calibration equation, and R(2) value, and quantitative analysis parameters were calculated for all of the analytes. Using different mobile phases, five different classes of aromatic hydrocarbons were separated in a very short analysis time of 4-8min. Furthermore, a high theoretical plate number (up to 25000) and an excellent peak asymmetry factor (1.0) were obtained. The results showed that the surface of the SWNTs had very strong interactions with aromatic groups, therefore providing high selectivity for the separation of different classes of aromatic compounds. This study indicates that SWCNTs enable the extension of the application range of the newly prepared stationary phases for the fast separation of aromatic compounds by HPLC. PMID:26717810

  6. Organic compounds in meteorites

    Science.gov (United States)

    Lawless, J. G.

    1980-01-01

    Recent studies of carbonaceous chondrites provide evidence that certain organic compounds are indigenous and the result of an abiotic, chemical synthesis. The results of several investigators have established the presence of amino acids and precursors, mono- and dicarboxylic acids, N-heterocycles, and hydrocarbons as well as other compounds. For example, studies of the Murchison and Murray meteorites have revealed the presence of at least 40 amino acids with nearly equal abundances of D and L isomers. The population consists of both protein and nonprotein amino acids including a wide variety of linear, cyclic, and polyfunctional types. Results show a trend of decreasing concentration with increasing carbon number, with the most abundant being glycine (41 n Moles/g). These and other results to be reviewed provide persuasive support for the theory of chemical evolution and provide the only natural evidence for the protobiological subset of molecules from which life on earth may have arisen.

  7. Synthesis of labeled compounds

    International Nuclear Information System (INIS)

    Intermediate compounds labeled with 13C included methane, sodium cyanide, methanol, ethanol, and acetonitrile. A new method for synthesizing 15N-labeled 4-ethylsulfonyl-1-naphthalene-sulfonamide was developed. Studies were conducted on pathways to oleic-1-13C acid and a second pathway investigated was based on carbonation of 8-heptadecynylmagnesium bromide with CO2 to prepare sterolic acid. Biosynthetic preparations included glucose-13C from starch isolated from tobacco leaves following photosynthetic incubation with 13CO2 and galactose-13C from galactosylglycerol-13C from kelp. Research on growth of organisms emphasized photosynthetic growth of algae in which all cellular carbon is labeled. Preliminary experiments were performed to optimize the growth of Escherichia coli on sodium acetate-13C

  8. Crystal structures of 2-methoxyisoindoline-1,3-dione, 1,3-dioxoisoindolin-2-yl methyl carbonate and 1,3-dioxo-2,3-dihydro-1H-benzo[de]isoquinolin-2-yl methyl carbonate: three anticonvulsant compounds

    Directory of Open Access Journals (Sweden)

    Fortune Ezemobi

    2014-12-01

    Full Text Available The title compounds, C9H7NO3, (1, C10H7NO5, (2, and C14H9NO5, (3, are three potentially anticonvulsant compounds. Compounds (1 and (2 are isoindoline derivatives and (3 is an isoquinoline derivative. Compounds (2 and (3 crystallize with two independent molecules (A and B in their asymmetric units. In all three cases, the isoindoline and benzoisoquinoline moieties are planar [r.m.s. deviations are 0.021 Å for (1, 0.04 and 0.018 Å for (2, and 0.033 and 0.041 Å for (3]. The substituents attached to the N atom are almost perpendicular to the mean planes of the heterocycles, with dihedral angles of 89.7 (3° for the N—O—Cmethyl group in (1, 71.01 (4 and 80.00 (4° for the N—O—C(=OO—Cmethyl groups in (2, and 75.62 (14 and 74.13 (4° for the same groups in (3. In the crystal of (1, there are unusual intermolecular C=O...C contacts of 2.794 (1 and 2.873 (1 Å present in molecules A and B, respectively. There are also C—H...O hydrogen bonds and π–π interactions [inter-centroid distance = 3.407 (3 Å] present, forming slabs lying parallel to (001. In the crystal of (2, the A and B molecules are linked by C—H...O hydrogen bonds, forming slabs parallel to (10-1, which are in turn linked via a number of π–π interactions [the most significant centroid–centroid distances are 3.4202 (7 and 3.5445 (7 Å], forming a three-dimensional structure. In the crystal of (3, the A and B molecules are linked via C—H...O hydrogen bonds, forming a three-dimensional structure, which is consolidated by π–π interactions [the most significant inter-centroid distances are 3.575 (3 and 3.578 (3 Å].

  9. Compound odontoma

    Directory of Open Access Journals (Sweden)

    Monica Yadav

    2012-01-01

    Full Text Available Odontomas have been extensively reported in the dental literature, and the term refers to tumors of odontogenic origin. Though the exact etiology is still unknown, the postulated causes include: local trauma, infection, inheritance and genetic mutation. The majority of the lesions are asymptomatic; however, may be accompanied with pain and swelling as secondary complaints in some cases. Here, we report a case of a compound odontome in a 14 year old patient.

  10. Magnesium compounds

    Science.gov (United States)

    Kramer, D.A.

    2006-01-01

    In 2005, seawater and natural brines accounted for 51% of US magnesium compounds production. World magnesia production was estimated to be 14.5 Mt. Most of the production came from China, North Korea, Russia and Turkey. Although no specific production figures are available, Japan and the United States are estimated to account for almost one-half of the world's capacity from seawater and brines.

  11. Tracing the biotransformation of polychlorinated biphenyls (PCBs) in common carp (Cryprinus carpio): Enantiomeric fraction and compound-specific stable carbon isotope analyses.

    Science.gov (United States)

    Tang, Bin; Luo, Xiao-Jun; Zeng, Yan-Hong; Sun, Run-Xia; Chen, Hua-Shan; Li, Zong-Rui; Mai, Bi-Xian

    2016-09-01

    Metabolites of polychlorinated biphenyls (PCBs) in fish are difficult to detect in vivo due to the complexity of biometabolism. In the present study, atropisomeric fraction analysis of chiral PCB congeners and compound-specific isotopic analysis (CSIA) were applied to trace the biotransformation of PCBs in fish by exposure of common carp (Cryprinus carpio) to the commercial PCB mixture Aroclor 1242. Stereoselective elimination of the chiral PCB congeners 91, 95, and 136 was observed, indicating a stereoselective biotransformation process. The δ(13)C values of PCBs 5/8, 18, and 20/33 in fish were increased compared with those in the spiked food, while PCBs 47/48 and 49 showed significant heavy isotope depletion. These results suggested a significant biotransformation of the corresponding individual PCB congeners although the potential PCB metabolites, hydroxylated PCBs (OH-PCBs) and methylsulfone PCBs (MeSO2-PCBs), were not detected in the fish tissue samples throughout this experiment. The results of the present study demonstrated that a combination of chiral analysis and CSIA is a promising new approach for investigating the biotransformation of PCBs in biota. PMID:27341148

  12. A study of using polythiol compounds and 2-ethyl-hexyl-acrylate with carbon tetrachloride as sensitizers for radiation vulcanization of natural rubber latex

    International Nuclear Information System (INIS)

    Experiments on using 3 different compounds of polythiol and an acrylate as sensitizer for radiation vulcanization were conducted. It was found that 1,4 butane diol propane tris-3-mercapto propionate showed the tendency to be a good sensitizer. The tensile strength of the rubber film prepared from the irradiated latex was found to be 14 MPa at sensitizer concentration of 1 phr and radiation dose of 45 kGy. As for 2-ethyl hexyl acrylate (2EHA), the maximum tensile strength of rubber film was found to be 23 MPa at concentration of 3 phr and radiation dose of 35 kGy. The mixture of 2 EHA and CCl4 at various ratio was also used as sensitizer. The optimum ratio was found to be 5:1 at concentration of 6 phr and radiation dose of 15 kGy. The maximum tensile strength was as high as 25 MPa. The study also revealed that the radiation vulcanized latex with crosslink density of about 18x1018 C.L./cm3 would give the rubber film of highest tensile strength

  13. Sorption of Tannin and Related Phenolic Compounds and Effects on Extraction of Soluble-N in Soil Amended with Several Carbon Sources

    Directory of Open Access Journals (Sweden)

    Javier M. Gonzalez

    2012-02-01

    Full Text Available Some tannins sorb to soil and reduce soluble-N. However, we know little about how they interact with organic amendments in soil. Soil (0–5 cm from plots, which were amended annually with various carbon substances, was treated with water (control or solutions containing tannins or related phenolic subunits. Treatments included a proanthocyanidin, catechin, tannic acid, β-1,2,3,4,6-penta-O-galloyl-D-glucose (PGG, gallic acid, and methyl gallate. We applied solutions of each of these materials to soil and measured soluble-C and -N in supernatants after application and following extraction with hot water (16 h, 80 °C. Sorption was low for non-tannin phenolics, methyl gallate, gallic acid, and catechin, and unaffected by amendment. Sorption of tannins, proanthocyanidin, tannic acid, and PGG, was higher and greater in plots amended with biosolids or manure. Extraction of soluble-N was not affected by amendment or by catechin, proanthocyanidin, or methyl gallate, but was reduced with PGG, tannic acid and gallic acid. Soil cation exchange capacity increased following treatment with PGG but decreased with gallic acid, irrespective of amendment. Tannins entering soil may thus influence soil organic matter dynamics and nutrient cycling but their impact may be influenced by the composition of soil organic matter.

  14. A new approach to understand methylmercury (CH3Hg) sources and transformation pathways: Compound-specific carbon stable isotope analysis by GC-C-IRMS

    Science.gov (United States)

    Baya, P. A.; Point, D.; Amouroux, D. P.; Lebreton, B.; Guillou, G.

    2015-12-01

    Methylmercury (CH3Hg) is a potent neurotoxin which is readily assimilated by organisms and bio-accumulates in aquatic food webs. In humans, consumption of CH3Hg contaminated marine fish is the major route of mercury exposure. However, our understanding of CH3Hg transformation pathways is still incomplete. To close this knowledge gap, we propose to explore the stable carbon isotopic composition (δ13C) of the methyl group of CH3Hg for a better understanding of its sources and transformation mechanisms. The method developed for the determination of the δ13C value of CH3Hg in biological samples involves (i) CH3Hg selective extraction, (ii) derivatization, and (iii) separation by gas chromatography (GC) prior to analysis by combustion isotope ratio mass spectrometry (C-IRMS). We present the figures of merit of this novel method and the first δ13C signatures for certified materials (ERM-CE464, BCR414) and biological samples at different marine trophic levels (i.e., tuna fish, zooplankton). The implications of this new approach to trace the pathways associated with Hg methylation and the mechanisms involved will be discussed.

  15. Mechanochemical reactions on copper-based compounds

    NARCIS (Netherlands)

    H.L. Castricum; H. Bakker; E.K. Poels

    1998-01-01

    Mechanochemical reactions of copper and copper oxides with oxygen and carbon dioxide are discussed, as well as decomposition and reduction of copper compounds by mechanical milling under high-vacuum conditions.

  16. New quaternary carbon and nitrogen stabilized polyborides: REB15.5CN (RE: Sc, Y, Ho, Er, Tm, Lu), crystal structure and compound formation

    International Nuclear Information System (INIS)

    A new family of quaternary carbon and nitrogen containing Rare Earth (RE: Sc, Y, Ho, Er, Tm and Lu) borides: REB15.5CN, has been synthesized and structurally characterized by powder X-ray diffraction data. They are all isotypic with Sc1-xB15.5CN whose structure was solved based on single-crystal X-ray data and HRTEM investigations. The structure refinement converged at a R(F2) value of 0.044 for 364 reflections. The new structure type of Sc1-xB15.5CN is composed of a three-dimensional network based on interconnected slabs of boron (B12)ico icosahedra and (B6)oct octahedra. A linear [CBC] chain and nitrogen tightly bridges icosahedra. Sc partially occupies voids in the sheets of boron octahedra. It crystallizes with the trigonal space group P3m1, with Z=2. Lattice parameters (nm) are as follows: for RE: Sc, a,b=0.5568(4), c=1.0756(2); Y, a,b=0.55919(6), c=1.0873(2); Ho, a,b=0.55883(7), c=1.0878(6); Er, a,b=0.55889(5), c=1.0880(6); Tm, a,b=0.5580(1), c=1.0850(6); Lu, a,b=0.55771(9), c=1.0839(4). Magnetic characterization of ErB17C1.3N0.6 has been performed

  17. Rate of uptake and distribution of Hg in dissolved organic carbon compounds in darkwater ecosystems by ICP-MS and enriched stable isotope spiking

    International Nuclear Information System (INIS)

    The role of natural organic acids on mercury binding, transportation, net uptake rates and possibly net methylation rates will be evaluated by tracing these processes with isotope enriched mercury and ICP-MS technology. The correlation between dissolved organic matter and Hg in waters is well documented. It appears that organic acids can react with mercury residing in or emitted from different sources such as soils (particularly hydromorphic soils), laterites, natural degassing, forest fires, fuel combustion, gold mining activities, etc. to form soluble Hg-organo-complexes. The formation of these complexes is believed to greatly enhance Hg transport and be an important preliminary step in the formation of Methyl-Hg and biological uptake. The rates of these reactions and the key organic compounds involved in mercury binding will be determined by reacting isotopically-enriched Hg with samples containing a variety of concentrations and types of organic acids and subsequently analysing both reactants and organisms exposed to the reactants (bioassays) for Hg isotopes by ICP-MS. The Hg spike will allow the precise determination of rates of uptake and the most active agents of uptake. Initially, the method will be used to examine total Hg uptake and distribution but if technological limitations are overcome, this same approach can be used to determine net rates of methylation and net MeHg uptake. After the method is validated the experimental design can be altered to test the relative effects of such things as the addition of CO2 (pH change), or adding a substrate such as Fe-Mn oxyhydroxides. The addition of synthetic materials such as mulched automobile tires, can also be tested with the goal developing a pragmatic remedial method for Hg containment. Ultimately, this research should contribute to an understanding of mercury mobilization, transport and bio-concentration mechanisms, and provide a basis for developing management and treatment strategies. Emphasis will be on

  18. Intermetallic Compounds

    Science.gov (United States)

    Takagiwa, Y.; Matsuura, Y.; Kimura, K.

    2014-06-01

    We have focused on the binary narrow-bandgap intermetallic compounds FeGa3 and RuGa3 as thermoelectric materials. Their crystal structure is FeGa3-type (tetragonal, P42/ mnm) with 16 atoms per unit cell. Despite their simple crystal structure, their room temperature thermal conductivity is in the range 4-5-W-m-1-K-1. Both compounds have narrow-bandgaps of approximately 0.3-eV near the Fermi level. Because their Seebeck coefficients are quite large negative values in the range 350-thermoelectric materials both by adjusting the carrier concentration and by reducing the thermal conductivity. Here, we report the effects of doping on the thermoelectric properties of FeGa3 and RuGa3 as n and p-type materials. The dimensionless figure of merit, ZT, was significantly improved by substitution of Sn for Ga in FeGa3 (electron-doping) and by substitution of Zn for Ga in RuGa3 (hole-doping), mainly as a result of optimization of the electronic part, S 2 σ.

  19. Evaluation of fused-core and monolithic versus porous silica-based C18 columns and porous graphitic carbon for ion-pairing liquid chromatography analysis of catecholamines and related compounds.

    Science.gov (United States)

    Chirita, Raluca-Ioana; Finaru, Adriana-Luminita; Elfakir, Claire

    2011-03-15

    This paper evaluates the performances of reversed-phase (RPLC) and ion-pairing chromatography (IPLC) coupled with UV detection for the analysis of a set of 12 catecholamines and related compounds. Different chromatographic columns (porous C18-silica, perfluorinated C18-silica, porous graphitic carbon, monolithic and fused-core silica-based C18 columns) were tested using semi-long perfluorinated carboxylic acids as volatile ion-pairing reagents. Much more promising results were obtained by IPLC than by RPLC and important improvements in analytes peak symmetry and separation resolution were observed when using the "fast chromatography" columns (monolithic and fused-core C18) under IPLC conditions. For UV detection, a satisfactory separation of the 12 selected analytes was achieved in less than 20 min by using a fused-core particles column (Halo C18) and a mobile phase composed of a 1.25 mM nonafluoropentanoic acid aqueous solution and methanol under gradient elution mode. The chromatographic method developed can be directly coupled with electrospray ionization tandem mass spectrometry (ESI-MS/MS) in positive ionization mode and 10 solutes among those selected can be observed. The presence of the acidic ion-pairing reagent in the mobile phase makes this system incompatible with negative ionization mode and thus unable to detect the two acidic compounds that only responded in negative mode. In terms of MS detection, Monolithic C18 column proved to be the best one to reach the lowest detection limits (LODs) (from 0.5 ngmL(-1) to 10 ngmL(-1) depending on the neurotransmitter). The applicability of the optimized LC-MS/MS method to a "real world" sample was finally evaluated. The presence of the matrix leads to signal suppression for several solutes and thus to higher LODs. PMID:21345749

  20. K- and L-edge X-ray absorption spectrum calculations of closed-shell carbon, silicon, germanium, and sulfur compounds using damped four-component density functional response theory.

    Science.gov (United States)

    Fransson, Thomas; Burdakova, Daria; Norman, Patrick

    2016-05-21

    X-ray absorption spectra of carbon, silicon, germanium, and sulfur compounds have been investigated by means of damped four-component density functional response theory. It is demonstrated that a reliable description of relativistic effects is obtained at both K- and L-edges. Notably, an excellent agreement with experimental results is obtained for L2,3-spectra-with spin-orbit effects well accounted for-also in cases when the experimental intensity ratio deviates from the statistical one of 2 : 1. The theoretical results are consistent with calculations using standard response theory as well as recently reported real-time propagation methods in time-dependent density functional theory, and the virtues of different approaches are discussed. As compared to silane and silicon tetrachloride, an anomalous error in the absolute energy is reported for the L2,3-spectrum of silicon tetrafluoride, amounting to an additional spectral shift of ∼1 eV. This anomaly is also observed for other exchange-correlation functionals, but it is seen neither at other silicon edges nor at the carbon K-edge of fluorine derivatives of ethene. Considering the series of molecules SiH4-XFX with X = 1, 2, 3, 4, a gradual divergence from interpolated experimental ionization potentials is observed at the level of Kohn-Sham density functional theory (DFT), and to a smaller extent with the use of Hartree-Fock. This anomalous error is thus attributed partly to difficulties in correctly emulating the electronic structure effects imposed by the very electronegative fluorines, and partly due to inconsistencies in the spurious electron self-repulsion in DFT. Substitution with one, or possibly two, fluorine atoms is estimated to yield small enough errors to allow for reliable interpretations and predictions of L2,3-spectra of more complex and extended silicon-based systems. PMID:27136720

  1. Compound odontoma

    Directory of Open Access Journals (Sweden)

    José Marcelo Vargas Pinto

    2008-01-01

    Full Text Available Odontomas are the most common types of odontogenic tumors, as they are considered more as a developmental anomaly (hamartoma than as a true neoplasia. The aim of the present study is to describe a clinical case of compound odontoma, analyzing its most commonsigns, its region of location, the decade of life and patient’s gender, disorders that may occur as well as the treatment proposed. In order to attain this objective, the method was description of the present clinical case and bibliographic revision, arriving at the result that the treatment for this type of lesion invariably is surgical removal (enucleation and curettage and the prognosis is excellent. The surgical result was followed up in the post-operative period by radiographic exam, and it was possible to conclude that there was complete cicatrization and tissue repair.

  2. 75 FR 3668 - Conditional Approval and Promulgation of State Implementation Plans; Ohio; Carbon Monoxide and...

    Science.gov (United States)

    2010-01-22

    ... (OAC) 3745-21 (Carbon Monoxide, Photochemically Reactive Materials, Hydrocarbons, and related Materials... compound containing carbon, excluding: Carbon monoxide, carbon dioxide; carbonic acid; metallic carbides... economic feasibility. On March 23, 1995, (60 FR 15235), EPA inadvertently approved a version of...

  3. Photocatalytic splitting of CS2 to S8 and a carbon-sulfur polymer catalyzed by a bimetallic ruthenium(II) compound with a tertiary amine binding site: toward photocatalytic splitting of CO2?

    Science.gov (United States)

    Livanov, Konstantin; Madhu, Vedichi; Balaraman, Ekambaram; Shimon, Linda J W; Diskin-Posner, Yael; Neumann, Ronny

    2011-11-21

    The catalytic photocleavage of CS(2) to S(8) and a (C(x)S(y))(n) polymer with visible light using a dinuclear ruthenium(II) compound with a bipyridine units for photoactivity and a vicinal tertiary amine binding site for CS(2) activation was studied. The catalyst was characterized by X-ray diffraction, (1)H NMR, and (13)C NMR, ESI-MS and elemental analysis. CS(2) photocleavage was significant (240 turnovers, 20 h) to yield isolable S(8) and a (C(x)S(y))(n) polymer. A mononuclear catalyst or one without an amine binding site showed significantly less activity. XPS of the (C(x)S(y))(n) polymer showed a carbon/sulfur ratio ∼1.5-1.6 indicating that in part both C-S bonds of CS(2) had been cleaved. Catalyst was also included within the polymer. The absence of peaks in the (1)H NMR verified the (C(x)S(y))(n) nature of the polymer, while (13)C NMR and IR indicated that the polymer had multiple types of C-S and C-C bonds. PMID:22029376

  4. Standard test method for the analysis of refrigerant 114, plus other carbon-containing and fluorine-containing compounds in uranium hexafluoride via fourier-transform infrared (FTIR) spectroscopy

    CERN Document Server

    American Society for Testing and Materials. Philadelphia

    2004-01-01

    1.1 This test method covers determining the concentrations of refrigerant-114, other carbon-containing and fluorine-containing compounds, hydrocarbons, and partially or completely substituted halohydrocarbons that may be impurities in uranium hexafluoride. The two options are outlined for this test method. They are designated as Part A and Part B. 1.1.1 To provide instructions for performing Fourier-Transform Infrared (FTIR) spectroscopic analysis for the possible presence of Refrigerant-114 impurity in a gaseous sample of uranium hexafluoride, collected in a "2S" container or equivalent at room temperature. The all gas procedure applies to the analysis of possible Refrigerant-114 impurity in uranium hexafluoride, and to the gas manifold system used for FTIR applications. The pressure and temperatures must be controlled to maintain a gaseous sample. The concentration units are in mole percent. This is Part A. 1.2 Part B involves a high pressure liquid sample of uranium hexafluoride. This method can be appli...

  5. Effect of Additives on Properties of Flame Retardant LLDPE with Magnesium Carbonate/Aluminium Hydroxide Compound%助剂对氢氧化铝和碳酸镁复配阻燃LLDPE性能的影响

    Institute of Scientific and Technical Information of China (English)

    李建新; 吴洁

    2011-01-01

    将协效剂白炭黑、硼酸锌、低熔点玻璃和硅烷偶联剂、铝酸脂偶联剂分别添加到碳酸镁/氢氧化铝复配阻燃的线型低密度聚乙烯(LLDPE)体系中,考察了这些助剂对体系阻燃性能和力学性能的影响.结果表明:几种助剂对体系的氧指数影响较小;白炭黑可以明显提高体系的拉伸强度,硼酸锌对体系的断裂伸长率影响最小;对拉伸强度而言,使用铝酸脂偶联剂优于硅烷偶联剂.%Several synergistic agents and two kind of coupling agents were added into the fame-retardant LLDPE system with magnesium carbonate and aluminium hydroxide compound, and the effects of additives on the flame retardant and mechanical properties of LLDPE system were studied.The results show that several synergistic agents have slight effect on oxygen index of the system, silica can improve the tensile strength evidently, and zinc borate has little influence on the elongation at break of the system. As far as the tensille strength is concerned, aluminate coupling agent is better than silane coupling agent.

  6. Effect of additives on magnesium carbonate and aluminium hydroxide compound with flame-retardant polyethylene system%添加剂对阻燃聚乙烯体系性能的影响

    Institute of Scientific and Technical Information of China (English)

    李建新; 吴洁

    2011-01-01

    为提高碳酸镁/氢氧化铝复配阻燃聚乙烯体系的性能,将几种常用协效剂和两种偶联剂添加到阻燃体系中,测量其阻燃性能及力学性能.实验表明:几种添加剂对提高体系的氧指数贡献相当;白炭黑可以明显提高体系的拉伸强度,硼酸锌对体系的断裂伸长率影响最小.对于拉伸强度、使用铝酸酯偶联剂效果优于硅烷偶联剂.%To improve the property of magnesium carbonate and aluminium hydroxide compound with flame-retardant PE sys tem,several synergistic agents and two kind of eoupling agents were added into the flame-retardant PE system. The fire retard ant property and mechanical property were tested. It indicates that several synergistic agents have similar contribution to oxy gen index of the system, silica white can improve the tenslle strength evidently, and zinc borate has little influence on the e longation at break of the system. As far as the tensile strength is concerned , aluminate coupling agent is better than silane cou pling agent.

  7. 碳-碳复合高性能无石棉密封板的研制%The Manufacture of High Performance Carbon-carbon Compound Non-asbestos Sealing Sheets

    Institute of Scientific and Technical Information of China (English)

    王仕江; 耿艳春; 吴益民

    2013-01-01

    该文在分析国内外无石棉密封材料现状基础上,以自主研制的改性短切碳纤维为增强材料、深加工的低密度柔性石墨微粉为主体填充材料、自制的高性能混合橡胶为粘合剂,组成了产品的主体配方.通过物料开松、混合、搅拌一体化等关键装备的研制和多层成张辊压等关键工艺参数的优化,成功制备了一种综合性能优良的碳-碳复合高性能无石棉密封板.与国内外无石棉密封板相比,在确保100%无石棉的基础上,具有更优异的耐温性和密封可靠性,可广泛应用于高温静态密封领域.%On the basis of the recent production technologies of non-asbestos sealing material,through using of key materials of Independently developed shot-cut carbon fiber (reinforced materials),low density flex graphite powder (main materials) and high performance rubber mixture (adhesive materials); through adopting of one step stirring-mixing equipment and multi-layer rolling methods,successfully manufacture a kind of high comprehensive performance non-asbestos sealing sheet.Comparing with other similar production,This sheets not only have the advantage of 100% non-asbestos content but also have higher stabilities of high temperature and seal,can be used in the fields about high temperature and static seal.

  8. Method to extract uranium compounds

    International Nuclear Information System (INIS)

    The uranium compounds present in gangue of phosphate ores are also to be determined and extracted with the proposed method. The gangue-water mixture in phosphate extraction is to be displaced, according to the invention, by a component which selectively dissolves the uranium compounds out of the gangue. The enriched solution is separated off and processed. Weak acids (e.g. phosphoric acid, acetre acid, citric acid), lyes (e.g. ammonium carbonate, soda) or salts (e.g. sodium hydrogen phosphate, NaHCO3 tartrates) are named as solution components. (UWI)

  9. Microbial growth on C1 compounds: proceedings

    International Nuclear Information System (INIS)

    This book contains individual papers prepared for the 4th International Symposium on Microbial Growth on One Carbon Compounds. Individual reports were abstracted and indexed for EDB. Topics presented were in the areas of the physiology and biochemistry of autotraps, physiology and biochemistry of methylotrophs and methanotrops, physiology and biochemistry of methanogens, genetics of microbes that use C1 compounds, taxonomy and ecology of microbes tht grow on C1 compounds, applied aspects of microbes that grow on C1 compounds, and new directions in C1 metabolism. (DT)

  10. Carbonation on ternary cement systems

    OpenAIRE

    Martínez Ramírez, Sagrario; Fernández Carrasco, Lucía

    2012-01-01

    The main hydration reaction product in the ternary system fly ash, calcium sulphate and calcium aluminate cement (40/20/40) at 20°C is a hydrated calcium sulfoaluminate compound, an AFt phase slightly different from “traditional ettringite”. The carbonation of ettringite develops gypsum but in this case rapidcreekite is formed. For the first time it has been observed that carbonation of the mentioned calcium sulfoaluminate compound (AFt), an hydrated calcium sulphate carbonated phase (Ca2(SO4...

  11. Asynchronous evolution of the isotopic composition and amount of precipitation in north China during the Holocene revealed by a record of compound-specific carbon and hydrogen isotopes of long-chain n-alkanes from an alpine lake

    Science.gov (United States)

    Rao, Zhiguo; Jia, Guodong; Li, Yunxia; Chen, Jianhui; Xu, Qinghai; Chen, Fahu

    2016-07-01

    Both the timing of the maximum East Asian summer monsoon (EASM) intensity in monsoonal China and the environmental significance of the Chinese stalagmite oxygen isotopic record (δ18O) have been debated. Here, we present a ca. 120-year-resolution compound-specific carbon (δ13C) and hydrogen (δD) isotopes of terrestrial long-chain n-alkanes extracted from a well-dated sediment core from an alpine lake in north China. Our δ13C data, together with previously reported pollen data from a parallel core, demonstrate a humid mid-Holocene from ca. 8-5 ka BP. Assuming that the climatic humidity of north China is an indicator of the EASM intensity, then the maximum EASM intensity occurred in the mid-Holocene. Our δD data reveal a similar long-term trend to the δ18O record from nearby Lianhua Cave, indicating that the synchronous δD and δ18O records faithfully record the δD and δ18O of precipitation, respectively. The most negative δD and δ18O values occur in the early-mid Holocene, from ca. 11-5 ka BP. This contrast in the timing of isotopic variations demonstrates a complex relationship between the isotopic composition of precipitation and precipitation amount, or EASM intensity. Further comparisons indicate a possible linkage between the precipitation amount in north China and the west-east thermal gradient in the equatorial Pacific. In addition, the temperature of the moisture source area may play an important role in determining the isotopic composition of precipitation in monsoonal China.

  12. Carbon dioxide as a carbon source in organic transformation: carbon-carbon bond forming reactions by transition-metal catalysts.

    OpenAIRE

    Tsuji, Yasushi; Fujihara, Tetsuaki

    2012-01-01

    Recent carbon-carbon bond forming reactions of carbon dioxide with alkenes, alkynes, dienes, aryl zinc compounds, aryl boronic esters, aryl halides, and arenes having acidic C-H bonds are reviewed in which transition-metal catalysts play an important role.

  13. Dispersion and separation of nanostructured carbon in organic solvents

    Science.gov (United States)

    Landi, Brian J. (Inventor); Raffaelle, Ryne P. (Inventor); Ruf, Herbert J. (Inventor); Evans, Christopher M. (Inventor)

    2011-01-01

    The present invention relates to dispersions of nanostructured carbon in organic solvents containing alkyl amide compounds and/or diamide compounds. The invention also relates to methods of dispersing nanostructured carbon in organic solvents and methods of mobilizing nanostructured carbon. Also disclosed are methods of determining the purity of nanostructured carbon.

  14. Volatile Organic Compounds (VOCs)

    Science.gov (United States)

    ... Organic Compounds' Impact on Indoor Air Quality Volatile Organic Compounds' Impact on Indoor Air Quality On this page: ... Exposure Standards or Guidelines Additional Resources Introduction Volatile organic compounds (VOCs) are emitted as gases from certain solids ...

  15. The synthesis of cementitious compounds in molten salts

    OpenAIRE

    Sheikh, R. A.

    2016-01-01

    This thesis describes an investigation into the synthesis of cementitious compounds in molten salts. These compounds are produced in energy-intensive industries (EIIs), such as the cement process, and are responsible for emitting significant quantities of carbon dioxide (CO2) emissions. Molten salt synthesis (MSS) involves dissolving compounds in a molten salt and reacting in solution. If the MSS of cementitious compounds can occur at lower temperatures than EIIs, this could lead to fewer qua...

  16. Preparation of azo compounds with solid catalysts

    OpenAIRE

    Corma, Avelino; García Gómez, Hermenegildo; Grirrane, Abdessamad

    2008-01-01

    [EN] The present invention refers to a procedure for preparing azo compounds comprising a reaction between at least: one amine or polyamine, molecular oxygen, a catalyst comprising at least one support selected fkom at least a metal oxide of one of the elements of the groups 3,4, 5, 6, 8, 9, 11 and 13, silica, an anionic laminar compound of hydrotalcite type or its derivatives, active carbon or an organic polymer. In addition, said catalyst may contain nanoparticles of gold.

  17. Electrochemical activation of reactions involving organometallic compounds

    International Nuclear Information System (INIS)

    Data on the electrochemical activation of various reactions involving organometallic compounds are generalised. Primary attention is devoted to the main types of transformation that can be performed by electrochemical electron transfer: redox activation of 16- and 18-electron complexes of transition metals, molybdenum, tungsten, and ruthenium in particular, as the first step of a broad range of reactions, electrocatalysis, mediator processes, and electrosynthesis of compounds containing carbon-metal σ-bonds

  18. PERFLUORINATED COMPOUNDS: EMERGING POPs WITH POTENTIAL IMMUNOTOXICITY

    OpenAIRE

    Corsini, Emanuela; Luebke, Robert W.; Germolec, Dori R.; DeWitt, Jamie C.

    2014-01-01

    Perfluorinated compounds (PFCs) have been recognized as an important class of environmental contaminants commonly detected in blood samples of both wildlife and humans. These compounds have been in use for more than 60 years as surface treatment chemicals, polymerization aids, and surfactants. They possess a strong carbon-fluorine bond, which leads to their environmental persistence. There is evidence from both epidemiology and laboratory studies that PFCs may be immunotoxic, affecting both c...

  19. 超声波辅助活性炭负载杂多酸盐催化合成尼泊金丁酯%CATALYTIC SYNTHESIS OF BUTYL PARABEN WITH ACTIVATED CARBON SUPPORTED HETEMPOLY COMPOUND BY ULTRASONIC ASSISTED METHOD

    Institute of Scientific and Technical Information of China (English)

    徐斌; 王雪源

    2012-01-01

    以对羟基苯甲酸和正丁醇为原料,活性炭负载Keggin型杂多酸盐[(CH2)5NH2]4SiM012O40为催化剂,在超声波辐射下合成尼泊金丁酯.考察了催化剂用量、原料配比、超声波辐射功率及辐射时间对尼泊金丁酯收率的影响.结果表明:超声波辐射下活性炭负载Keggin型杂多酸盐[(CH2)5NH2]4SiMo12O40具有良好的催化活性.较佳工艺条件为:对羟基苯甲酸4.14 g(0.03 mol),酸醇摩尔比1.0:2.0,环己烷40 mL,催化剂7g,450 W超声波辐射20 min.尼泊金丁酯收率达到97%以上.%The butyl paraben was synthesized with p-hydroxy benzoic acid and n-butanol by ultrasonic assisted method, with activated carbon supported keggin-structured hetempoly compound, [(CH2)5NH2]4SiMo12O40, as catalysts. Effects of catalyst dosage, molar ratios of the reactants, ultrasonic wave power and radiation time were investigated. The results showed that the catalytic activity is good under ultrasonic and the optimal conditions were determined as follows: p-hydroxy benzoic 4. 14 g (0. 03 mol), mole ratio of p-hydroxy benzoic acid to n-butanol 1.0 : 2. 0, cyclohexane 40 mL, catalyst 7 g as well as radiation time 20 min with the ultrasonic wave power of 450 W. Under these conditions, the yield of butyl paraben was up to 97%.

  20. 水中氯代烃单体碳同位素分析中预富集方法进展%Review on Pre-enrichment Methods in Compound Specific Carbon Isotope Analysis of Chlorinated Hydrocarbon in Water

    Institute of Scientific and Technical Information of China (English)

    凌媛; 黄毅; 尚文郁; 谢曼曼; 刘舒波; 孙青

    2011-01-01

    Highly accurate determination of Compound Specific Carbon Isotope Analysis ( CSIA ) of chlorinated hydrocarbons is of great significance in tracing the source and revealing the biodegradating progress of pollutants. The isotopic composition of organic contaminations may be stable or varied in the process of environmental transformation. We can trace the source of contaminations if the composition is stable and can evaluate the probability and degree of degradation of contaminations. This paper summarizes solid-phase microextraction, static headspace analysis, purge and trap method and compound specific isotope analyses of chlorinated hydrocarbon in water, using combinations of these pretreatment methods, Gas Chromatography-Combustion-Isotope Ratio Mass Spectrometry ( GC-C-IRMS ), and comparesthe three methods. Compared with liquid-liquid extraction, solid-phase micro extraction, static headspace analysis, purge and trap method are all solvent-free enrichment techniques, producing no secondary pollution, less interference, and the resolution and accuracy of the analysis of GC-C-IRMS is improved. No, or little, isotopic mass fractionation occurred during the isotope analysis of chlorinated hydrocarbon in water by combining these solvent-free enrichment techniques with GC-C-IRMS, of which the precision of the analysis is less than l%e. The detection limit decreased along with the methods of static headspace analysis, solid-phase micro extraction, purge and trap method. Purge and trap is the most popular method because of its good reproducibility and low detection limit for the compound specific isotope analysis of chlorinated hydrocarbon in Water. The combinations of in-needle microextraction, in-tube microextraction, stir bar sorptive extraction or headspace sorptive extraction with GC-C-IRMS have a bright future.%高精度准确测定氯代烃单体碳同位素对示踪污染物来源,了解污染物的生物降解过程具有重要意义.在环境转化过程中,

  1. Heuristics for chemical compound matching.

    Science.gov (United States)

    Hattori, Masahiro; Okuno, Yasushi; Goto, Susumu; Kanehisa, Minoru

    2003-01-01

    We have developed an efficient algorithm for comparing two chemical compounds, where the chemical structure is treated as a 2D graph consisting of atoms as vertices and covalent bonds as edges. Based on the concept of functional groups in chemistry, 68 atom types (vertex types) are defined for carbon, nitrogen, oxygen, and other atomic species with different environments, which has enabled detection of biochemically meaningful features. Maximal common subgraphs of two graphs can be found by searching for maximal cliques in the association graph, and we have introduced heuristics to accelerate the clique finding. Our heuristic procedure is controlled by some adjustable parameters. Here we applied our procedure to the latest KEGG/LIGAND database with different sets of parameters, and demonstrated the correlation of parameters in our algorithm with the distribution of similarity scores and/or the execution time. Finally, we showed the effectiveness of our heuristics for compound pairs along metabolic pathways. PMID:15706529

  2. Michael Addition Reaction of Fluorinated Nitro Compounds

    Institute of Scientific and Technical Information of China (English)

    郇凤; 胡华伟; 黄焰根; 陈庆云; 郭勇

    2012-01-01

    The Michael addition reactions of fluorinated nitro compounds with electron deficient olefins to give γ-fiuoro-γ-nitro-esters, nitriles and ketones which bear a fluorinated quaternary carbon center were reported. The reactions were promoted by TMG, affording the desired adducts in acceptable to good yields.

  3. Reflectance spectroscopy of organic compounds: 1. Alkanes

    Science.gov (United States)

    Clark, R.N.; Curchin, J.M.; Hoefen, T.M.; Swayze, G.A.

    2009-01-01

    Reflectance spectra of the organic compounds comprising the alkane series are presented from the ultraviolet to midinfrared, 0.35 to 15.5 /??m. Alkanes are hydrocarbon molecules containing only single carbon-carbon bonds, and are found naturally on the Earth and in the atmospheres of the giant planets and Saturn's moon, Titan. This paper presents the spectral properties of the alkanes as the first in a series of papers to build a spectral database of organic compounds for use in remote sensing studies. Applications range from mapping the environment on the Earth, to the search for organic molecules and life in the solar system and throughout the. universe. We show that the spectral reflectance properties of organic compounds are rich, with major diagnostic spectral features throughout the spectral range studied. Little to no spectral change was observed as a function of temperature and only small shifts and changes in the width of absorption bands were observed between liquids and solids, making remote detection of spectral properties throughout the solar system simpler. Some high molecular weight organic compounds contain single-bonded carbon chains and have spectra similar to alkanes even ' when they fall into other families. Small spectral differences are often present allowing discrimination among some compounds, further illustrating the need to catalog spectral properties for accurate remote sensing identification with spectroscopy.

  4. Determination of nicotine, tar, volatile organic compounds and carbonyls in mainstream cigarette smoke using a glass filter and a sorbent cartridge followed by the two-phase/one-pot elution method with carbon disulfide and methanol.

    Science.gov (United States)

    Uchiyama, Shigehisa; Hayashida, Hideki; Izu, Rina; Inaba, Yohei; Nakagome, Hideki; Kunugita, Naoki

    2015-12-24

    We have developed a new analytical method for the determination of nicotine, tar, volatile organic compounds and carbonyls in main-stream cigarette smoke using a sorbent cartridge packed with Carboxen 572 (CX-572) and a Cambridge filter pad (CFP) followed by the two-phase/one-pot elution method. A CX-572 cartridge is installed between the intake of the CFP and the pump of the smoking machine. Gaseous compounds collected with the CX-572 cartridge and total particulate matter (TPM) collected with the CFP are coeluted simultaneously in the same vial and then analyzed by high-performance liquid chromatography (HPLC), gas chromatography-mass spectrometry (GC/MS) and gas chromatograph-thermal conductivity detector (GC/TCD). Carbonyl compounds are determined by adding derivatizing reagent (2,4-dinitrophenylhydrazine, DNPH) to the eluate followed by HPLC analysis. VOCs and nicotine are determined by GC/MS, and water is determined by GC/TCD. The same sample eluate solution is used for HPLC, GC/MS and GC/TCD analyses. As a result of measuring main-stream cigarette smoke generated from reference cigarettes, almost all carbonyl compounds and VOCs except formaldehyde were passed through a CFP and trapped in a CX-572 cartridge. 100% of nicotine, tar and TPM were trapped in a CFP. 50% of water and 53% of formaldehyde were trapped in a CFP. The one-pot data is almost equal to the sums of CFP (particulate matter) and CX-572 (gaseous compounds) data. The two-phase/one-pot elution method can simultaneously measure nicotine, tar, volatile organic compounds and carbonyl compounds in cigarette smoke with simple operation and small amounts of reagents. PMID:26653840

  5. Carbon Alloys-Multi-functionalization

    Energy Technology Data Exchange (ETDEWEB)

    Yasuda, Eiichi [MSL, Tokyo Institute of Technology, Yokohama 226-8503 (Japan)], E-mail: yasuda.e.aa.@m.titech.ac.jp; Enami, Takashi; Hoteida, Nobuyuki [MSL, Tokyo Institute of Technology, Yokohama 226-8503 (Japan); Lanticse-Diaz, L.J. [University of the Philippines (Philippines); Tanabe, Yasuhiro [Nagoya University (Japan); Akatsu, Takashi [MSL, Tokyo Institute of Technology, Yokohama 226-8503 (Japan)

    2008-02-25

    Last decade after our proposal of the 'Carbon Alloys' concept, many different kinds of Carbon Alloys, such as carbon nanotubes, carbon nanofibers, graphene sheet with magnetism, semi-conducting BCN compounds, graphite intercalation compounds, exfoliated carbon fiber, etc. have been found and developed. To extend the concept further, it is important to make it into intelligent materials by incorporating multiple functions. One example of the multi-functionalization is the development of homo-atomic Carbon Alloys from glassy carbon (GC) that exhibits high electrical conductivity and low gas permeability after treatment at critical conditions. Glassy carbon underwent metamorphosis to graphite spheres at HIP condition, and improved resistance to oxidation after alloying with Ta. The other one is shape utilization of the nano-sized carbon by understanding the effect of its large surfaces or interfaces in nanotechnology treatment. Recently carbon nanofiber was produced by polymer blend technology (PB) which was proposed by Prof. A. Oya during the Carbon Alloy project and progressed into intelligent carbon nanofiber (CNF) materials. CNF is combined into the polymer composites which is a candidate material for the bipolar separator in fuel cell. The superior properties, i.e., high electrical conductivity, high modulus, high strength, etc., of the CNF is being utilized in the preparation of this polymer composite.

  6. Specific features and the mechanism of the adsorption of carbon monoxide on the surface of films prepared from solid solutions and binary compounds of the InSb-ZnSe system

    International Nuclear Information System (INIS)

    Adsorption properties (towards CO) of solid solutions and binary compounds in the system InSb-ZnSe in the range of 273-553 K were studied and compared. The previously identified acid-base and other physicochemical characteristics of the adsorbents were used for analyzing the results obtained. By comparing adsorption properties of the binary compounds (InSb, ZnSe) and solid solutions (InSb)x(ZnSe)1-x their common features in behavior and specific features of the solid solutions as multicomponent systems were revealed. The mechanism and regularities of the adsorption processes, depending on occurrence conditions and system composition, were ascertained

  7. Einstein relation in compound semiconductors and their nanostructures

    CERN Document Server

    Bhattacharya, Sitangshu

    2008-01-01

    Deals with the Einstein relation in compound semiconductors and their nanostructures. This book considers materials such as nonlinear optical, III-V, ternary, quaternary, II-VI, IV-VI, Bismuth, stressed compounds, quantum wells, quantum wires, nipi structures, carbon nanotubes, heavily doped semiconductors, and inversion layers.

  8. Carbon Carbon Composites: An Overview .

    OpenAIRE

    G. Rohini Devi; K. Rama Rao

    1993-01-01

    Carbon carbon composites are a new class of engineering materials that are ceramic in nature but exhibit brittle to pseudoplastic behaviour. Carbon-carbon is a unique all-carbon composite with carbon fibre embeded in carbon matrix and is known as an inverse composite. Due to their excellent thermo-structural properties, carbon-carbon composites are used in specialised application like re-entry nose-tips, leading edges, rocket nozzles, and aircraft brake discs apart from several indust...

  9. Carbon storage in forest soil

    International Nuclear Information System (INIS)

    The article reviews research on short and long term carbon storage. A Norwegian programme with the objective of increasing knowledge of key processes which govern the carbon storage and loss of CO2 from forest soil in Norway is mentioned. Topics that will be studied are: The production and loss of CO2 from the soil, root ecology, the microorganism ability of degrading organic compounds, transport and loss of organic compounds through the soil to creeks and lakes and the modelling of carbon currents and storage in various forest ecosystems both in the soil and above

  10. Thiophenic Sulfur Compounds Released During Coal Pyrolysis.

    Science.gov (United States)

    Xing, Mengwen; Kong, Jiao; Dong, Jie; Jiao, Haili; Li, Fan

    2013-06-01

    Thiophenic sulfur compounds are released during coal gasification, carbonization, and combustion. Previous studies indicate that thiophenic sulfur compounds degrade very slowly in the environment, and are more carcinogenic than polycyclic aromatic hydrocarbons and nitrogenous compounds. Therefore, it is very important to study the principle of thiophenic sulfur compounds during coal conversion, in order to control their emission and promote clean coal utilization. To realize this goal and understand the formation mechanism of thiophenic sulfur compounds, this study focused on the release behavior of thiophenic sulfur compounds during coal pyrolysis, which is an important phase for all coal thermal conversion processes. The pyrolyzer (CDS-5250) and gas chromatography-mass spectrometry (Focus GC-DSQII) were used to analyze thiophenic sulfur compounds in situ. Several coals with different coal ranks and sulfur contents were chosen as experimental samples, and thiophenic sulfur compounds of the gas produced during pyrolysis under different temperatures and heating rates were investigated. Levels of benzothiophene and dibenzothiophene were obtained during pyrolysis at temperatures ranging from 200°C to 1300°C, and heating rates ranging from 6°C/ms to 14°C/ms and 6°C/s to 14°C/s. Moreover, the relationship between the total amount of benzothiophene and dibenzothiophene released during coal pyrolysis and the organic sulfur content in coal was also discussed. This study is beneficial for understanding the formation and control of thiophenic sulfur compounds, since it provides a series of significant results that show the impact that operation conditions and organic sulfur content in coal have on the amount and species of thiophenic sulfur compounds produced during coal pyrolysis. PMID:23781126

  11. Microstructural and compositional Evolution of Compound Layers during Gaseous Nitrocarburizing

    DEFF Research Database (Denmark)

    Du, Hong; Somers, Marcel A.J.; Ågren, John

    Compound layers developed at 848 K during gaseous nitrocarburizing of iron and iron-carbon specimens were investigated for several combinations of N and C activities imposed at the specimen surface by gas mixtures of NH3, N2, CO2 and CO. The microstructural evolution of the compound layer was...... evolution and the growth kinetics of the compound layers formed is discussed for the iron substrate. The results indicate that the microstructure is governed by a fast C and a slow N absorption at the surface in an early stage of gaseous nitrocarburizing. The influence of carbon in the substrate on the...

  12. Calcium carboorthovanadate - a new compound with the apa

    International Nuclear Information System (INIS)

    Data on calcium carboorthovanadate, Ca10(VO4)6CO3, a new compound with an appatite structure based on calcium orthovanadate, are reported. The synthesis has been conducted in a stoichiometric mixture of finely ground calcium carbonate and calcium orthovanadate. It is found that calcium carboorthovanadate belongs to the hexagonal syngony and has an apatite structure. An analysis of the infrared spectra of initial compounds and calcium carboorthovanadate confirmed the presence of carbonate (CO3)2- and orthovanadate (VO4)3 groupings in the latter. On heating in air, beginning with 450 deg C calcium carboorthovanadate decomposes at a slow rate into calcium oxide, calcium orthovanadate, and carbon dioxide

  13. Synthesis Organic Compound

    OpenAIRE

    Rasyid, Herlina; Firdaus; Hariani, Nunuk

    2015-01-01

    Abstract. Synthesis of metil ??-(p-hidroksifenil)akrilic from ??-(p-hidroksifenil)akrilat acid and methanol using Dean Stark Trap method had been done. Synthesis of ths compound intended to form the starting material in the subsequent synthesis of amide???s compound through the formation of ester compound. This synthesis using H2SO4 catalyst and Dean Stark Trap method, some of benzena which is added to remove the water that resulting from the reaction. Synthesis of this compound be held at re...

  14. On labelled compounds nomenclature

    International Nuclear Information System (INIS)

    Different approaches of major labelled compounds producers to their nomenclature in technical and commercial documentation are discussed. Some draft options of a standard technical guide document for labelled compounds nomenclature rules are suggested. Such a document after due discussion by the experts will serve to unification of the labelled compounds nomenclature within the frame of the CMEA member-countries co-operation in this field. The suggested options are based on the general recommendations by the International Union of Pure and Applied Chemistry and incorporate some more accurate definitions originating from the labelled compounds production and application experience

  15. Carbon cycle: A hump in ocean-air exchange

    Science.gov (United States)

    Reddy, Christopher M.

    2016-06-01

    Semivolatile organic compounds from fossil fuels or incomplete combustion are ubiquitous. A suite of circumglobal measurements of their oceanic and atmospheric concentrations reveals large carbon fluxes through the deposition of these compounds.

  16. Process for forming a metal compound coating on a substrate

    International Nuclear Information System (INIS)

    This patent describes a method of coating a substrate with a thin layer of a metal compound by forming a dispersion of an electrophoretically active organic colloid and a precursor of the metal compound in an electrolytic cell in which the substrate is an electrode. Upon application of an electric potential, the electrode is coated with a mixture of the organic colloid and the precursor to the metal compound, and the coated substrate is then heated in the presence of an atmosphere or vacuum to decompose the organic colloid and form a coating of either a combination of metal compound and carbon, or optionally forming a porous metal compound coating by heating to a temperature high enough to chemically react the carbon

  17. NATURAL POLYACETYLENE COMPOUNDS

    Directory of Open Access Journals (Sweden)

    D. A. Konovalov

    2014-01-01

    Full Text Available Polyacetylenes (polyynes are compounds which contain two or more triple bonds in its structure. About 2 000 different polyacetylenes and biogenetically related substances were identified in 24 families of higher plants. However, most of these compounds were found in seven families of flowering plants: Apiaceae (Umbelliferae, Araliaceae, Asteraceae (Compositae, Campanulaceae, Olacaceae, Pittosporaceae and Santalaceae. Polyacetylenes are relatively unstable, chemically and biologically active compounds, and present in fungi, microorganisms, marine invertebrates and other organisms except for plants. Acetylenes form distinct specialized group of chemically active natural compounds, which are biosynthesized in plants of unsaturated fatty acids. In addition to widespread aliphatic polyacetylenes thiophenes dithiacyclohexadienes (thiarubrines, thioethers, sulphoxides, sulphones, alkamides, chlorohydrins, lactones, spiroacetal enol ethers, furans, pyrans, tetrahydropyrans, isocoumarins, aromatic acetylenes were also found in plant species. Polyacetylenes are localized in different plant organs, and can be found both individually and as a compound with carbohydrates, terpene, phenolic and other compounds. Many polyacetylenes are found in the composition of the essential oils of plants and it confirms their strongly marked ecological functions. From biological point of view these compounds are often synthesized by plants as toxic or bitter antifeedants, allelopathic compounds, phytoalexins or broadly antibiotic components. Polyynes are strong photosensitizers. They exhibit anti-inflammatory, anti-coagulant, anti-bacterial, antituberculosis, anti-fungal, anti-viral, neuroprotective and neurotoxic activity. Immunostimulatory influence associated with certain allergenicity of some of these substances was established. Therefore, without a doubt polyacetylenes are of interest for the modern pharmacy and medicine.

  18. Stable isotopes labelled compounds

    International Nuclear Information System (INIS)

    The catalogue on stable isotopes labelled compounds offers deuterium, nitrogen-15, and multiply labelled compounds. It includes: (1) conditions of sale and delivery, (2) the application of stable isotopes, (3) technical information, (4) product specifications, and (5) the complete delivery programme

  19. NATURAL POLYACETYLENE COMPOUNDS

    OpenAIRE

    D. A. Konovalov

    2014-01-01

    Polyacetylenes (polyynes) are compounds which contain two or more triple bonds in its structure. About 2 000 different polyacetylenes and biogenetically related substances were identified in 24 families of higher plants. However, most of these compounds were found in seven families of flowering plants: Apiaceae (Umbelliferae), Araliaceae, Asteraceae (Compositae), Campanulaceae, Olacaceae, Pittosporaceae and Santalaceae. Polyacetylenes are relatively unstable, chemically and biologically activ...

  20. Mini Total Organic Carbon Analyzer (miniTOCA) Project

    Data.gov (United States)

    National Aeronautics and Space Administration — Total Organic Carbon (TOC) analyzers function by converting (oxidizing) all organic compounds (contaminants) in the water sample to carbon dioxide gas (CO2), then...

  1. Nomenclature for labelled compounds

    International Nuclear Information System (INIS)

    This paper report on isotopically labelled compounds. The first indexing system for isotopically labelled organic compounds is generally credited to Boughton and named after him. An extension of his principles for designating compounds containing hydrogen isotopes has been part of the Chemical Abstracts Service index nomenclature system for many years. After close on five years labor the IUPAC sponsored Commission on Nomenclature of Organic Chemistry presented in 1979 their findings on Isotopically Modified Compounds. The system codified in their rules provides for recognition of various types of isotopic modification and is therefore of more general applicability. Concurrently the rules for the nomenclature of isotopically modified inorganic compounds are developed. These are to be seen as supplementing and extending the guidelines laid down in the IUPAC Inorganic Nomenclature Rules already published

  2. Biokinetics of radioactive compounds

    International Nuclear Information System (INIS)

    Biokinetics of radioactive compounds in the human organism represent the central notion in this work, consisting of a theoretical and an experimental part. The first chapter contains definitions and explanations on the importance of the biokinetics of radioactive compounds in clinical therapy and pharmaceuticals research as well as for assessing radiation exposure and radiation hazards. Chapter 2 describes the bases of the biokinetics of radioactive compounds in the medical and non-medical sector, and biokinetics. Chapter 3 deals with obtaining biokinetics data for radioactive compounds from investigations in animals and man, evaluation of measurements, transferring data obtained by animal experiments to man, and with the variability of biokinetics data. In Chapter 4 the results of comprehensive studies in literature on the biokinetics of radioactive compounds are summarized. They relate to three areas: professional and environmental incorporation of radioactive compounds, use of radioactive pharmaceuticals in therapy and research, and incorporation of radioactive compounds by embryo and fetus in consequence of the uptake of radioactive compounds by the mother. Chapter 5 gives an assessment of radiation hazards from radioactive compounds in connection with occupational radiation exposure and nuclear diagnostics in vivo, and a comparison with other risks. For that purpose the concept of effective dose equivalent is applied in connection with suitable risk coefficients to professional and nuclear-medical radiation exposure. Chapter 6 is dedicated to measurement of the biokinetics of radioactive compounds in man using conventional devices. The object of Chapter 7 is measurement of the biokinetics of radioactive pharmaceuticals in man by means of single photon emission computed tomography. (orig./MG)

  3. Crystallography, semiconductivity, thermoelectricity, and other properties of boron and its compounds, especially B6O

    Science.gov (United States)

    Slack, G. A.; Morgan, K. E.

    2015-09-01

    Electron deficient and non-deficient boron compounds are discussed as potential thermoelectric generator materials. Particular attention is paid to carbon-doped beta-boron, high-carbon boron carbide, and the alpha-boron derivative compound boron suboxide. Stoichiometric B6O shows some promise, and may have a higher ZT than the other two compounds. Carbon saturated beta-boron appears to have a higher ZT than undoped samples. Carbon saturated boron carbide at B12C3 does exist. Its thermoelectric behavior is unknown.

  4. Carbon in Atmospheric Particulate Matter

    International Nuclear Information System (INIS)

    Carbon compounds account for a large fraction of airborne particulate matter ('carbonaceous aerosols'). Their presence raises a number of scientific questions dealing with climate issues and possible effects on human health. This review describes the current state of knowledge with respect to the ambient concentrations levels (elemental carbon, organic carbon and organic matter) and the various emission sources, and summarizes the role of atmospheric carbon in the various environmental issues. The report finishes by identifying the actual gaps in knowledge and gives (related) suggestions for future research

  5. Carbon nanotubes: a suitable material for catalytic wet peroxide oxidation of organic pollutants?

    OpenAIRE

    Ribeiro, Rui; Silva, Adrián; Faria, Joaquim; Gomes, Helder

    2012-01-01

    Carbon materials, such as activated carbons (AC), graphite and activated carbon xerogels, have been explored as metal-free catalysts for the catalytic wet peroxide oxidation (CWPO) of bio-refractory organic compounds, such as azo dyes and phenolic compounds [1-3]. At the same time, the application of carbon nanomaterials in catalysis, such as carbon nanotubes (CNT), has grown exponentially [4]. In the present work, commercial multiwalled carbon nanotubes (MWNT) were used in the CWPO of 2-nitr...

  6. Evaluation of bioremediation systems utilizing stable carbon isotope analysis

    International Nuclear Information System (INIS)

    Carbon, whether in an organic or inorganic form, is composed primarily of two stable isotopes, carbon-12 and carbon-13. The ratio of carbon-12 to carbon-13 is approximately 99:1. The stable carbon isotope ratios of most natural carbon materials of biological interest range from approximately 0 to -110 per mil (per-thousand) versus the PDB standard. Utilizing stable carbon isotope analysis, it is often possible to determine the source(s) of the liberated carbon dioxide, thereby confirming successful mineralization of the targeted carbon compound(s) and, if the carbon dioxide results from multiple carbon compounds, in what ratio the carbon compounds are mineralized. Basic stable isotope 'theory' recommended sampling procedures and analysis protocols are reviewed. A case study involving fuel oil presented on the application of stable carbon isotope analysis for the monitoring and evaluation of in situ bioremediation. At the site, where a field bioventing study was being conducted, multiple potential sources of carbon dioxide production existed. Additional potential applications of stable carbon isotope analysis for bioremediation evaluation and monitoring are discussed

  7. 不同碳源催化化学气相沉积制备自支撑C/Ni-Fiber复合电极材料的电容脱盐性能%Self-supporting Macroscopic Carbon/Ni-Fiber Hybrid Electrodes Prepared by Catalytic Chemical Vapor Deposition Using Various Carbonaceous Compounds and Their Capacitive Deionization Performance

    Institute of Scientific and Technical Information of China (English)

    王喜文; 姜芳婷; 索全伶; 方玉珠; 路勇

    2011-01-01

    以甲烷、乙烯、乙醇和正丁醇为碳源,通过催化化学气相沉积在具有三维开放网络结构的烧结8 μm-Ni金属纤维上沉积碳的方法,制备了以金属Ni纤维网络为集流极、沉积碳为离子存储库的薄层大面积自支撑C/Ni-fiber复合电极材料.用扫描电子显微镜(SEM)、透射电子显微镜(TEM)、热重分析(TGA)、X射线衍射(XRD)、N2-吸脱附等温线和循环伏安与电化学阻抗谱对电极材料进行了表征,并考察了其作为电极的电容脱盐性能.乙烯、甲烷、正丁醇和乙醇为碳源的沉积碳形态分别为鱼骨状碳纳米管(CNTs)、石墨烯面取向与轴平行的CNTs、棒状和蠕虫状碳纳米纤维(CNFs).C/Ni-fiber复合电极材料对NaCl的电吸附容量顺序为:乙烯>正丁醇>甲烷>乙醇,这与复合电极的电化学特性、孔结构和碳的纳米结构相关.在1.2V的工作电压下,以乙烯为碳源制备的C/Ni-fiber复合电极材料对水溶液中NaCl (100 mg·L-1)的电吸附容量达159 μmol·g-1.%We prepared a series of self-supported macroscopic C/Ni-fiber hybrid electrodes by catalytic chemical vapor deposition (CCVD) using methane, ethylene, ethanol and n-butanol as carbon sources to embed carbon onto a three-dimensional network of sinter-locked conductive 8 um-nickel fibers. For the as-prepared hybrid electrodes, the Ni-microfibrous network serves as a current collector and the carbons as ion storage media while the macroporous void space serves as an electrolyte reservoir. We characterized the hybrid electrodes using scanning electron microscopy (SEM), transmission electron microscopy (TEM), thermogravimetric analysis (TGA), X-ray diffraction (XRD), N2 isothermal adsorption-desorption, cyclic voltammetry and electrochemical impedance spectroscopy. The desalination performance of the C/Ni-fiber hybrids was evaluated as electrodes in a capacitive deionization system. The carbon morphology is dependent on the carbonaceous compounds

  8. Compound composite odontoma

    Directory of Open Access Journals (Sweden)

    G Girish

    2016-01-01

    Full Text Available The term odontoma has been used as a descriptor for any tumor of odontogenic origin. It is a growth in which both epithelial and mesenchymal cells exhibits complete differentiation. Odontomas are considered as hamartomas rather than true neoplasm. They are usually discovered on routine radiographic examination. Odontomas, according to the World Health Organization, are classified into complex odontoma and compound odontomas. The present paper reports a case of compound composite odontomas.

  9. Compound composite odontoma.

    Science.gov (United States)

    Girish, G; Bavle, Radhika M; Singh, Manish Kumar; Prasad, Sahana N

    2016-01-01

    The term odontoma has been used as a descriptor for any tumor of odontogenic origin. It is a growth in which both epithelial and mesenchymal cells exhibits complete differentiation. Odontomas are considered as hamartomas rather than true neoplasm. They are usually discovered on routine radiographic examination. Odontomas, according to the World Health Organization, are classified into complex odontoma and compound odontomas. The present paper reports a case of compound composite odontomas. PMID:27194882

  10. Compounding a Problem?

    Science.gov (United States)

    Berlin, Joey

    2016-01-01

    Allergist-immunologists say a U.S. Pharmacopeia proposal will mess with an allergy treatment system that's worked for more than a century. The revised standards, if adopted, would remove a key exemption separating allergen extract preparations from the stricter requirements of other compounds. Immunologists say the exemption has allowed them to compound allergen extracts in their own offices, and they've done so safely and effectively millions of times a year. PMID:27175928

  11. Phenolic compounds in flaxseed

    OpenAIRE

    Johnsson, Pernilla

    2004-01-01

    The dietary lignan secoisolariciresinol diglucoside (SDG), present in high concentrations in flaxseed, and its metabolites enterolactone and enterodiol are thought to decrease the risk of hormone dependent cancers, cardiovascular disease and other “welfare” diseases. Flaxseed also contains other biologically active phenolic compounds, such as phenolic acids. The understanding of the nature of these compounds is crucial for their possible exploitation in drugs and functional foods. Until the m...

  12. INSENSITIVE HIGH-NITROGEN COMPOUNDS

    Energy Technology Data Exchange (ETDEWEB)

    D. CHAVEZ; ET AL

    2001-03-01

    The conventional approach to developing energetic molecules is to chemically place one or more nitro groups onto a carbon skeleton, which is why the term ''nitration'' is synonymous to explosives preparation. The nitro group carries the oxygen that reacts with the skeletal carbon and hydrogen fuels, which in turn produces the heat and gaseous reaction products necessary for driving an explosive shock. These nitro-containing energetic molecules typically have heats of formation near zero and therefore most of the released energy is derived from the combustion process. Our investigation of the tetrazine, furazan and tetrazole ring systems has offered a different approach to explosives development, where a significant amount of the chemical potential energy is derived from their large positive heats of formation. Because these compounds often contain a large percentage of nitrogen atoms, they are usually regarded as high-nitrogen fuels or explosives. A general artifact of these high-nitrogen compounds is that they are less sensitive to initiation (e.g. by impact) when compared to traditional nitro-containing explosives of similar performances. Using the precursor, 3,6-bis-(3,5-dimethylpyrazol-1-yl)-s-tetrazine, several useful energetic compounds based on the s-tetrazine system have been synthesized and studied. Some of the first compounds are 3,6-diamino-s-tetrazine-1,4-dioxide (LAX-112) and 3,6-dihydrazino-s-tetrazine (DHT). LAX-112 was once extensively studied as an insensitive explosive by Los Alamos; DHT is an example of a high-nitrogen explosive that relies entirely on its heat of formation for sustaining a detonation. Recent synthesis efforts have yielded an azo-s-tetrazine, 3,3'-azobis(6-amino-s-tetrazine) or DAAT, which has a very high positive heat of formation. The compounds, 4,4'-diamino-3,3'-azoxyfurazan (DAAF) and 4,4'-diamino-3,3'-azofurazan (DAAzF), may have important future roles in insensitive explosive

  13. Scientific Opinion on safety and efficacy of cobalt compounds (E3 as feed additives for all animal species: Cobaltous acetate tetrahydrate, basic cobaltous carbonate monohydrate and cobaltous sulphate heptahydrate, based on a dossier submitted by TREAC EEIG

    Directory of Open Access Journals (Sweden)

    EFSA Panel on Additives and Products or Substances used in Animal Feed

    2012-07-01

    Full Text Available

    Cobalt(III is a component of cobalamin. Its essentiality as trace element results from the capacity of certain animal species to synthesise cobalamin by the gastrointestinal microbiota. Feeding supplemental cobalt from the additives under application up to the maximum total content in feed set in EU is considered safe for all animal species/categories; margin of safety is around 10. Cobalt is predominantly excreted via faecal route. Absorbed cobalt follows aqueous excretion routes. About 43% of body cobalt is stored in muscle; however, kidney and liver are the edible tissues containing the highest cobalt concentrations and are most susceptible reflecting dietary cobalt concentrations. In animals with capacity to synthesise cobalamin, cobalt is also deposited in tissues as vitamin B12. Cobalt(II cations are genotoxic under in vitro and in vivo conditions, and have carcinogen, mutagen and reproduction toxicant (CMR properties. No data are available on the potential carcinogenicity of cobalt(II following oral exposure. However, oral exposure may potentially entail adverse threshold-related effects in humans. The estimated population intake of cobalt most likely includes the contribution of foodstuffs from animals fed cobalt-supplemented feedingstuffs. An increase in cobalt exposure by the use of cobalt-containing feed additives is therefore not expected. Considering the population exposure to cobalt, about 4–10 times lower than the health-based guidance value, no safety concern for the consumer is expected for threshold effects of oral cobalt. The cobalt(II compounds assessed are considered skin and eye irritants and dermal/inhalatory sensitisers. Their dust is a hazard to persons handling these substances. Exposure by inhalation must be avoided. The use of cobalt from any source at the authorised maximum content in feed does not provide a risk to the environment. The compounds assessed are available for cobalamin

  14. The compound ethers of glycerin

    International Nuclear Information System (INIS)

    In this chapter of book authors describe several methods of receiving of compound ethers of glycerin. The important technic significance have compound glycerin ether and nitric acid. This compound receive by reaction of glycerin with fuming nitric acid

  15. CARBON NANOTUBES AND PHARMACEUTICAL APPLICATIONS

    OpenAIRE

    Ram Pavani; Kodithyala Vinay

    2011-01-01

    Carbon nanotubes (CNTs) are often described as a graphene sheet rolled up into the shape of a cylinder. These have fascinated scientists with their extraordinary properties. These compounds have become increasingly popular in various fields simply because of their small size and amazing optical, electric and magnetic properties when used alone or with additions of metals. Carbon nanotubes have potential therapeutic applications in the field of drug delivery, diagnostics, and biosensing. Funct...

  16. Gas chromatographic isolation technique for compound-specific radiocarbon analysis

    International Nuclear Information System (INIS)

    Full text: We present here a gas chromatographic isolation technique for the compound-specific radiocarbon analysis of biomarkers from the marine sediments. The biomarkers of fatty acids, hydrocarbon and sterols were isolated with enough amount for radiocarbon analysis using a preparative capillary gas chromatograph (PCGC) system. The PCGC systems used here is composed of an HP 6890 GC with FID, a cooled injection system (CIS, Gerstel, Germany), a zero-dead-volume effluent splitter, and a cryogenic preparative collection device (PFC, Gerstel). For AMS analysis, we need to separate and recover sufficient quantity of target individual compounds (>50 μgC). Yields of target compounds from C14 n-alkanes to C40 to C30 n-alkanes and approximately that of 80% for higher molecular weights compounds more than C30 n-alkanes. Compound specific radiocarbon analysis of organic compounds, as well as compound-specific stable isotope analysis, provide valuable information on the origins and carbon cycling in marine system. Above PCGC conditions, we applied compound-specific radiocarbon analysis to the marine sediments from western north Pacific, which showed the possibility of a useful chronology tool for estimating the age of sediment using organic matter in paleoceanographic study, in the area where enough amounts of planktonic foraminifera for radiocarbon analysis by accelerator mass spectrometry (AMS) are difficult to obtain due to dissolution of calcium carbonate. (author)

  17. Catalytic reforming of model tar compounds from hot coke oven gas with low steam/carbon ratio over Ni/MgO-Al{sub 2}O{sub 3} catalysts

    Energy Technology Data Exchange (ETDEWEB)

    Yue, Baohua [Department of Chemistry, College of Sciences, Shanghai University, Shanghai 200444 (China); Wang, Xueguang; Ai, Xinpeng; Yang, Jun; Li, Lin; Lu, Xionggang; Ding, Weizhong [Shanghai Key Laboratory of Modern Metallurgy and Material Processing, Shanghai University, Yanchang Road No.149, Shanghai 200072 (China)

    2010-09-15

    The catalytic reforming of toluene and naphthalene was performed to investigate the possibility for directly converting tar components from hot coke oven gas (COG) with lower steam/carbon (S/C) molar ratios to light fuel gases. The NiO/MgO-Al{sub 2}O{sub 3} catalysts reduced exhibited excellent catalytic activity, stability and sulphur tolerance. The effects of various reaction conditions and S/C ratios on the catalytic performance were investigated in detail. Toluene and naphthalene were completely converted into small gas molecules at 700-800 C and S/C = 0.28. An appropriate amount of steam benefited the methanation reaction of CO and H{sub 2}. The effects of N{sub 2}, CH{sub 4} or CO in COG were also discussed. Relative to N{sub 2}, CO contributed to the conversion of toluene and the formation of CH{sub 4}, but the opposite was true for CH{sub 4}. The sulphur tolerance was tested by adding H{sub 2}S in the feed gas. The reaction results were explained by a water cycle mechanism. (author)

  18. Thermal and oxidation stability of organo-fluorine compound-mixed electrolyte solutions for lithium ion batteries

    Science.gov (United States)

    Nishikawa, Daiki; Nakajima, Tsuyoshi; Ohzawa, Yoshimi; Koh, Meiten; Yamauchi, Akiyoshi; Kagawa, Michiru; Aoyama, Hirokazu

    2013-12-01

    Thermal and oxidation stability of fluorine compound-mixed electrolyte solutions have been investigated. Charge/discharge behavior of natural graphite electrode has been also examined in the same electrolyte solutions. Fluorine compounds demonstrate much lower reactivity with metallic Li than ethylene carbonate/dimethyl carbonate. Fluorine compound-mixed electrolyte solutions show the lower reactivity with LiC6 and the smaller exothermic peaks due to decomposition of electrolyte solutions and surface films than original solutions without fluorine compound. Oxidation currents are also smaller in fluorine compound-mixed electrolyte solutions than in original ones. First coulombic efficiencies in fluorine compound-mixed electrolyte solutions are similar to those in original ethylene carbonate-based solutions except one case. Mixing of fluorine compounds highly increase first coulombic efficiencies of natural graphite electrode in propylene carbonate-containing solution.

  19. Atmospheric emissions in metropolitan France: compounds related to the increase of the greenhouse effect

    International Nuclear Information System (INIS)

    This report presents and comments statistical data and indicators on emissions of compounds involved in the greenhouse effect: carbon dioxide (CO2), methane (CH4), nitrogen dioxide (NO2), hydro-fluorocarbon compounds (HFCs), per-fluorocarbon compounds (PFCs), sulphur hexafluoride (SF6). For these compounds, the report indicates and comments world and French emission data, their evolution, and the shares of different sectors and their evolutions. It also comments the evolution of the global warming potential (GWP)

  20. Terahertz Spectroscopy of Biochars and Related Aromatic Compounds

    Science.gov (United States)

    Lepodise, L. M.; Horvat, J.; Lewis, R. A.

    2016-07-01

    A recent application of terahertz spectroscopy is to biochar, the agricultural charcoal produced by pyrolysis of various organic materials. Biochars simultaneously improve soil fertility and assist in carbon sequestration. Terahertz spectroscopy allows different biochars to be distinguished. However, the origin of the absorption features observed has not been clear. Given that biochar-based fertilizers are rich in aromatic compounds, we have investigated simple aromatic compounds as an approach to unravelling the complex biochar spectrum.

  1. Chromium (V) compounds as cathode material in electrochemical power sources

    Science.gov (United States)

    Delnick, F.M.; Guidotti, R.A.; McCarthy, D.K.

    A cathode for use in a thermal battery, comprising a chromium (V) compound. The preferred materials for this use are Ca/sub 5/(CrO/sub 4/)/sub 3/Cl, Ca/sub 5/(CrO/sub 4/)OH, and Cr/sub 2/O/sub 5/. The chromium (V) compound can be employed as a cathode material in ambient temperature batteries when blended with a suitably conductive filler, preferably carbon black.

  2. Compound management beyond efficiency.

    Science.gov (United States)

    Burr, Ian; Winchester, Toby; Keighley, Wilma; Sewing, Andreas

    2009-06-01

    Codeveloping alongside chemistry and in vitro screening, compound management was one of the first areas in research recognizing the need for efficient processes and workflows. Material management groups have centralized, automated, miniaturized and, importantly, found out what not to do with compounds. While driving down cost and improving quality in storage and processing, researchers still face the challenge of interfacing optimally with changing business processes, in screening groups, and with external vendors and focusing on biologicals in many companies. Here we review our strategy to provide a seamless link between compound acquisition and screening operations and the impact of material management on quality of the downstream processes. Although this is driven in part by new technologies and improved quality control within material management, redefining team structures and roles also drives job satisfaction and motivation in our teams with a subsequent positive impact on cycle times and customer feedback. PMID:19502566

  3. Fluorine-18 labelled compounds

    International Nuclear Information System (INIS)

    The work presented in this thesis deals with the problems involved in the adaption of reactor-produced fluorine-18 to the synthesis of 18F-labelled organic fluorine compounds. Several 18F-labelling reagents were prepared and successfully applied. The limitations to the synthetic possibilities of reactor-produced fluoride-18 become manifest in the last part of the thesis. An application to the synthesis of labelled aliphatic fluoro amino acids has appeared to be unsuccessful as yet, although some other synthetic approaches can be indicated. Seven journal articles (for which see the availability note) are used to compose the four chapters and three appendices. The connecting text gives a survey of known 18F-compounds and methods for preparing such compounds. (Auth.)

  4. Compound semiconductor device physics

    CERN Document Server

    Tiwari, Sandip

    2013-01-01

    This book provides one of the most rigorous treatments of compound semiconductor device physics yet published. A complete understanding of modern devices requires a working knowledge of low-dimensional physics, the use of statistical methods, and the use of one-, two-, and three-dimensional analytical and numerical analysis techniques. With its systematic and detailed**discussion of these topics, this book is ideal for both the researcher and the student. Although the emphasis of this text is on compound semiconductor devices, many of the principles discussed will also be useful to those inter

  5. Synthesizing labeled compounds

    International Nuclear Information System (INIS)

    A metabolic study is presented of the chemical reactions provided by isotopic labeling and NMR spectroscopy. Synthesis of 13C-labeled D-glucose, a 6-carbon sugar, involves adding a labeled nitrile group to the 5-carbon sugar D-arabinose by reaction with labeled hydrogen cyanide. The product of this reaction is then reduced and hydrolyzed to a mixture of the labeled sugars. The two sugars are separated by absorption chromotography. The synthesis of 13C-labeled L-tyrosine, an amino acid, is also presented

  6. Radiocarbon dating of organic compounds in sediments using preparative capillary gas chromatography (PCGC)

    Energy Technology Data Exchange (ETDEWEB)

    Uchida, Masao [Japan Marine Science and Technology Center, Yokosuka, Kanagawa (Japan); Shibata, Yasuyuki; Yoneda, Minoru; Mukai, Hitoshi; Tanaka, Atsushi; Uehiro, Takashi; Morita, Masatoshi [National Inst. for Environmental Studies, Tsukuba, Ibaraki (Japan); Kawamura, Kimitaka [Hokkaido Univ., Sapporo (Japan); Hirota, Masashi [National Inst. for Environmental Studies, Tsukuba, Ibaraki (Japan)

    2001-02-01

    CG-AMS system, combining two-dimensional gas chromatography and accelerator mass spectroscopy, has been developed for compound-specific carbon 14 measurement. Samples from shallow sea sediments in Sanbanse, Tokyo bay ware collected, six typical fatty acids were separated therefrom. Ages were estimated from the carbon 14 measurement. Acids of carbon number 15 and 16 has nearly contemporary age, whereas acids of carbon number 22 has age of 17000 years. (A. Yamamoto)

  7. Flavour Compounds in Fungi

    DEFF Research Database (Denmark)

    Ravasio, Davide Antonio

    Fungi produce a variety of volatile organic compounds (VOCs) during their primary or secondary metabolism and with a wide range of functions. The main focus of this research work has been put on flavour molecules that are produced during fermentation processes, mainly esters and alcohols derived...

  8. Forecasting of superconducting compounds

    International Nuclear Information System (INIS)

    In forecasting new superconducting intermetallic compounds of the A15 and Mo3Se types most promising from the viewpoint of high critical temperature Tsub(c), high critical magnetic fields Hsub(c), and high critical currents and in estimating their transition temperature it is proposed to apply cybernetic methods of computer learning

  9. Chemical compounds in teak

    Directory of Open Access Journals (Sweden)

    Fernanda Viana da Silva Leonardo

    2015-09-01

    Full Text Available Quinone compounds are largely generated at extractive fraction of the woods in a complex and variable biological system. The literature has indications for many segments from food industry to pharmaceutical industry. Within the field of industrial use of wood, they are less desirable since they are treated only as incidental substances in production strings of pulp, paper, charcoal, and sawmill. In spite of its small amount, compared to other chemical compounds called essential, these substances have received special attention from researchers revealing a diverse range of offerings to market products textiles, pharmaceuticals, colorants, and other polymers, for which are being tested and employed. Quinones are found in fungi, lichens, and mostly in higher plants. Tectona grandis, usually called teak, is able to biosynthesize anthraquinones, which is a quinone compound, byproduct of secondary metabolism. This species provides wood that is much prized in the furniture sector and can also be exploited for metabolites to supply the market in quinone compounds and commercial development of new technologies, adding value to the plantations of this species within our country.

  10. NATURAL POLYACETYLENE COMPOUNDS

    Directory of Open Access Journals (Sweden)

    A. M. Nasukhova

    2014-01-01

    Full Text Available In article the review of the initial stage of researches of natural polyacetylene compounds is resulted. The high reactionary ability leading to fast oxidation and degradation of these compounds, especially at influence of Uf-light, oxygen of air, pH and other factors, has caused the serious difficulties connected with an establishment of structure and studying of their physical and chemical properties. Therefore the greatest quantity of works of this stage is connected with studying of essential oils of plants from families Apiaceae, Araliaceae, Asteraceae, Campanulaceae, Olacaceae, Pittosporaceae and Santalaceae where have been found out, basically, diacetylene compounds. About development of physical and chemical methods of the analysis of possibility of similar researches have considerably extended. More than 2000 polyacetylenes are known today, from them more than 1100 are found out in plants fam. Asteraceae. Revolution in the field of molecular biology has allowed to study processes of biosynthesis of these compounds intensively.

  11. Stabilization of labelled compounds

    International Nuclear Information System (INIS)

    This invention concerns a composition including a labelled compound, and the vitamin B 12. This vitamin gives a red colour to the solution and stabilize it radiochemically, allowing to transport the solution at ambient temperature and a storage at 4 degrees celsius. (N.C.). 5 refs

  12. Compound floating pivot micromechanisms

    Science.gov (United States)

    Garcia, Ernest J.

    2001-04-24

    A new class of tilting micromechanical mechanisms have been developed. These new mechanisms use compound floating pivot structures to attain far greater tilt angles than are practical using other micromechanical techniques. The new mechanisms are also capable of bi-directional tilt about multiple axes.

  13. Fissibility of compound nuclei

    CERN Document Server

    Iwata, Yoritaka

    2012-01-01

    Collisions between $^{248}$Cm and $^{48}$Ca are systematically investigated by time-dependent density functional calculations with evaporation prescription. Depending on the incident energy and impact parameter, fusion, deep-inelastic and fission events are expected to appear. In this paper, a microscopic method of calculating the fissibility of compound nuclei is presented.

  14. Carbon nanotubes composites for microwave applications

    OpenAIRE

    Herrero Fernández, Diego

    2015-01-01

    Carbon nanotubes have become a focus of study due to the great applications you can have and its excellent properties. In this thesis the compounds formed by a host and a percentage of carbon nanotubes are modelled. The models used are the Debye model, the Maxwell Garnett model and McLachlan model. These models have been implemented in ...

  15. The Path of Carbon in Photosynthesis VI.

    Science.gov (United States)

    Calvin, M.

    1949-06-30

    This paper is a compilation of the essential results of our experimental work in the determination of the path of carbon in photosynthesis. There are discussions of the dark fixation of photosynthesis and methods of separation and identification including paper chromatography and radioautography. The definition of the path of carbon in photosynthesis by the distribution of radioactivity within the compounds is described.

  16. Synthesis and applications of isotopically labelled compounds 1994. Proceedings

    International Nuclear Information System (INIS)

    The 5th International Symposium on the Synthesis and Applications of Isotopically Labelled Compounds, 1994, concentrated on the following topics: - the synthesis, analysis and applications of organic compounds labelled with hydrogen and tritium, the production of stable radioactive isotopes such as cobalt 60, germanium 68, holmium 166, dysprosium 166 and tungsten 188; the synthesis of organic compounds labelled with short-lived isotopes such as carbon 11. The uses of isotopes in agriculture, nutrition, pharmaceutical research, pharmacology, medicine and biological pathways was discussed. The final section reviews the regulations governing the safety, handling and disposal of radioisotopes worldwide. (UK)

  17. Researches on vanadium and its compounds

    International Nuclear Information System (INIS)

    In this research thesis, the author proposes a new study of the action of some reduction agents on two groups of vanadium compounds, oxides and chlorides. Thus, he reports the study of the circumstances of reduction of vanadium oxides by carbon and of vanadium carburization from these compounds. He also reports the determination of the composition of vanadium melts obtained at high temperatures (either in a vacuum furnace or with an electric arc furnace). In order to determine in which conditions the processing of vanadium oxides could produce the pure metal, the author studied the action of calcium and magnesium on the vanadium pentoxide and trioxide. The second part of the thesis addresses the preparation of pure vanadium from vanadium anhydride chlorides. Then, the author reports the development of processes which could easily produce powdered vanadium

  18. Baseline isotopic data of polyhalogenated compounds

    International Nuclear Information System (INIS)

    The δ 2H- and δ 13C-values of polyhalogenated compounds were determined by EA-IRMS. Most of the compounds were related to the chloropesticides DDT and its metabolites, hexachlorocyclohexanes, and toxaphene, as well as several polybrominated compounds such as bromophenols and -anisoles. δ 2H-values ranged between -235 per mille and +75 per mille whereas δ 13C-values were found in the range -22 per mille to -38 per mille . No correlation between δ 2H- and δ 13C-values could be identified. Comparative analysis clarified that bromophenols and the corresponding bromoanisoles may vary in their isotopic distribution. 2H NMR was used to quantify abundances of 2H isotopomers. Quantification of isotopomers of 2,4-dibromophenol and 2,4-dibromoanisole proved that both compounds from different suppliers do not originate from the same source. Differences in the δ 2H-values of two toxaphene products were further investigated by the synthesis of products of different degree of chlorination from camphene. It was shown that the δ 13C-values remained mostly unaltered as was expected since no carbon is lost in this procedure. However, the reaction products became enriched in 2H with increasing degree of chlorination. Different δ 2H-values of the starting material will also impact the δ 2H-values of the chlorination products

  19. Transformation and utilization of carbon dioxide

    Energy Technology Data Exchange (ETDEWEB)

    Bhanage, Bhalchandra M. [Institute of Chemical Technology, Mumbai (India). Dept. of Chemistry; Arai, Masahiko (ed.) [Hokkaido Univ., Sapporo (Japan). Division of Chemical Process Engineering

    2014-04-01

    This book shows the various organic, polymeric and inorganic compounds which result from the transformation of carbon dioxide through chemical, photocatalytic, electrochemical, inorganic and biological processes. The book consists of twelve chapters demonstrating interesting examples of these reactions, depending on the types of reaction and catalyst. It also includes two chapters dealing with the utilization of carbon dioxide as a reaction promoter and presents a wide range of examples of chemistry and chemical engineering with carbon dioxide.

  20. A novel crystalline SiCO compound.

    Science.gov (United States)

    Marqués, Miriam; Morales-García, Angel; Menéndez, José Manuel; Baonza, Valentín G; Recio, José Manuel

    2015-10-14

    Ab initio evolutionary structural searches have been performed on SixCyO2(x+y) compounds. A novel structure, with SiC2O6 stoichiometry and the P21/c space group is calculated to be stable against decomposition within a wide pressure window from 7.2 to 41 GPa, and metastable under ambient conditions. It consists of CO3 units, linked to SiO6 octahedra, supporting previous experimental studies. The evolution of the carbon environment towards tetrahedral CO4 units, thus resembling the crystal chemistry of silicon, is predicted at higher pressures. PMID:26345349

  1. Compound semiconductor device modelling

    CERN Document Server

    Miles, Robert

    1993-01-01

    Compound semiconductor devices form the foundation of solid-state microwave and optoelectronic technologies used in many modern communication systems. In common with their low frequency counterparts, these devices are often represented using equivalent circuit models, but it is often necessary to resort to physical models in order to gain insight into the detailed operation of compound semiconductor devices. Many of the earliest physical models were indeed developed to understand the 'unusual' phenomena which occur at high frequencies. Such was the case with the Gunn and IMPATI diodes, which led to an increased interest in using numerical simulation methods. Contemporary devices often have feature sizes so small that they no longer operate within the familiar traditional framework, and hot electron or even quantum­ mechanical models are required. The need for accurate and efficient models suitable for computer aided design has increased with the demand for a wider range of integrated devices for operation at...

  2. Erupted compound odontome

    Directory of Open Access Journals (Sweden)

    Shekar S

    2009-01-01

    Full Text Available Odontomas are considered to be hamartomas rather than a true neoplasm. They consist chiefly of enamel and dentin, with variable amount of pulp and cementum when fully developed. They are generally asymptomatic and are included under the benign calcified odontogenic tumors. They are usually discovered on routine radiographic examination. Eruption of an odontoma in the oral cavity is rare. Peripheral compound odontomas arise extraosseously and have a tendency to exfoliate. In this article we are reporting a case of a 15-year-old girl with peripheral compound odontoma, with a single rudimentary tooth-like structure in the mandibular right second molar region, which is about to be exfoliated. Its eruption in the oral cavity and location in the mandibular posterior region is associated with aplasia of the mandibular right second molar, making it an interesting case for reporting.

  3. Endocrine disrupting compounds

    DEFF Research Database (Denmark)

    Bøgh, I B; Christensen, P; Dantzer, V;

    2001-01-01

    With the growing concern that environmental chemicals might impair human and animal fertility, it is important to investigate the possible influence of these substances on sexual differentiation and genital development of mammals. Many of these substances are suspected to interfere with endocrine...... of alkylphenols, these are disseminated in the environment with sewage sludge, and domestic animals and humans are likely to be exposed via the food chain. Using the pig as an in vivo model, we studied the effect of intrauterine exposure to tertiary octylphenol (OP) on essential reproductive...... usefulness of in vivo animal or embryo models for the evaluation of possible consequences of human exposure to endocrine disrupting compounds is discussed. Furthermore, possible consequences of exposure to endocrine disrupting compounds for the embryo transfer industry are addressed....

  4. Compound Chondrules fused Cold

    CERN Document Server

    Hubbard, Alexander

    2015-01-01

    About 4-5% of chondrules are compound: two separate chondrules stuck together. This is commonly believed to be the result of the two component chondrules having collided shortly after forming, while still molten. This allows high velocity impacts to result in sticking. However, at T ~ 1100K, the temperature below which chondrules collide as solids (and hence usually bounce), coalescence times for droplets of appropriate composition are measured in tens of seconds. Even at 1025K, at which temperature theory predicts that the chondrules must have collided extremely slowly to have stuck together, the coalescence time scale is still less than an hour. These coalescence time scales are too short for the collision of molten chondrules to explain the observed frequency of compound chondrules. We suggest instead a scenario where chondrules stuck together in slow collisions while fully solid; and the resulting chondrule pair was subsequently briefly heated to a temperature in the range of 900-1025K. In that temperatur...

  5. Hydrogen in compound semiconductors

    Energy Technology Data Exchange (ETDEWEB)

    Haller, E.E.

    1993-05-01

    Progress in the understanding of hydrogen and its interactions in III/V and II/VI compound semiconductors is reviewed. Donor, acceptor and deep level passivation is well established in III/V compounds based on electrical measurements and on spectroscopic studies. The hydrogen donor levels in GaAs and GaP are estimated to lie near E{sub v}+0.5 eV and E{sub v}+0.3 eV, respectively. Arsenic acceptors have been passivated by hydrogen in CdTe and the very first nitrogen-hydrogen local vibrational model spectra in ZnSe have been reported. This long awaited result may lead to an explanation for the poor activation of nitrogen acceptors in ZnSe grown by techniques which involve high concentrations of hydrogen.

  6. Labelled compounds. (Pt. B)

    International Nuclear Information System (INIS)

    Since the end of World War II there has been a tremendous increase in the number of compounds that have been synthesized with radioactive or stable isotopes. They have found application in many diverse fields, so much so, that hardly a single area in pure and applied science has not benefited. Not surprisingly it has been reflected in appearance of related publications. The early proceedings of the Symposia on Advances in Trace Methodology were soon followed by various Euratom sponsored meetings in which methods of preparing and storing labelled compounds featured prominently. In due course a resurgence of interest in stable isotopes, brought about by their greater availability (also lower cost) and partly by development of new techniques such as gas chromatography - mass spectrometry (gc-ms), led to the publication of proceedings of several successful conferences. More recently conferences dealing with the synthesis and applications of isotopes and isotopically labelled compounds have been established on a regular basis. In addition to the proceedings of conferences and journal publications individuals left their mark by producing definitive texts, usually on specific nuclides. Only the classic two volume publication of Murray and Williams (Organic syntheses with isotopes, New York 1985), now over 30 years old and out of print, attempted to do justice to several nuclides. With the large amount of work that has been undertaken since then it seems unlikely that an updated edition could be produced. The alternative strategy was to ask scientists currently active to review specific areas and this is the approach adopted in the present series of monographs. In this way it is intended to cover the broad advances that have been made in the synthesis and applications of isotopes and isotopically labelled compounds in the physical and biomedical sciences. (author). refs.; figs.; tabs

  7. Phenolic compounds in oats

    OpenAIRE

    Skoglund, Maria

    2008-01-01

    This research project examined how to treat raw oat material for oat-based food products in order to sustain or increase the levels of phenolic compounds. The focus was mainly on the avenanthramides, which are potentially health beneficial bioactive components found exclusively in oats. A proposed enzymatic decrease in avenanthramide levels when non heat-treated milled oats are steeped in water was investigated. The decrease was strongly suggested to be caused by a polyphenol oxidase. Althoug...

  8. Compound chondrules fused cold

    Science.gov (United States)

    Hubbard, Alexander

    2015-07-01

    About 4-5% of chondrules are compound: two separate chondrules stuck together. This is commonly believed to be the result of the two component chondrules having collided shortly after forming, while still molten. This allows high velocity impacts to result in sticking. However, at T ∼ 1100 K, the temperature below which chondrules collide as solids (and hence usually bounce), coalescence times for droplets of appropriate composition are measured in tens of seconds. Even at 1025 K, at which temperature theory predicts that the chondrules must have collided extremely slowly to have stuck together, the coalescence time scale is still less than an hour. These coalescence time scales are too short for the collision of molten chondrules to explain the observed frequency of compound chondrules. We suggest instead a scenario where chondrules stuck together in slow collisions while fully solid; and the resulting chondrule pair was subsequently briefly heated to a temperature in the range of 900-1025 K. In that temperature window the coalescence time is finite but long, covering a span of hours to a decade. This is particularly interesting because those temperatures are precisely the critical window for thermally ionized MRI activity, so compound chondrules provide a possible probe into that vital regime.

  9. Compound Wiretap Channels

    Directory of Open Access Journals (Sweden)

    Shlomo Shamai (Shitz

    2009-01-01

    Full Text Available This paper considers the compound wiretap channel, which generalizes Wyner's wiretap model to allow the channels to the (legitimate receiver and to the eavesdropper to take a number of possible states. No matter which states occur, the transmitter guarantees that the receiver decodes its message and that the eavesdropper is kept in full ignorance about the message. The compound wiretap channel can also be viewed as a multicast channel with multiple eavesdroppers, in which the transmitter sends information to all receivers and keeps the information secret from all eavesdroppers. For the discrete memoryless channel, lower and upper bounds on the secrecy capacity are derived. The secrecy capacity is established for the degraded channel and the semideterministic channel with one receiver. The parallel Gaussian channel is further studied. The secrecy capacity and the secrecy degree of freedom (s.d.o.f. are derived for the degraded case with one receiver. Schemes to achieve the s.d.o.f. for the case with two receivers and two eavesdroppers are constructed to demonstrate the necessity of a prefix channel in encoder design. Finally, the multi-antenna (i.e., MIMO compound wiretap channel is studied. The secrecy capacity is established for the degraded case and an achievable s.d.o.f. is given for the general case.

  10. Compound Wiretap Channels

    Directory of Open Access Journals (Sweden)

    Kramer Gerhard

    2009-01-01

    Full Text Available Abstract This paper considers the compound wiretap channel, which generalizes Wyner's wiretap model to allow the channels to the (legitimate receiver and to the eavesdropper to take a number of possible states. No matter which states occur, the transmitter guarantees that the receiver decodes its message and that the eavesdropper is kept in full ignorance about the message. The compound wiretap channel can also be viewed as a multicast channel with multiple eavesdroppers, in which the transmitter sends information to all receivers and keeps the information secret from all eavesdroppers. For the discrete memoryless channel, lower and upper bounds on the secrecy capacity are derived. The secrecy capacity is established for the degraded channel and the semideterministic channel with one receiver. The parallel Gaussian channel is further studied. The secrecy capacity and the secrecy degree of freedom ( are derived for the degraded case with one receiver. Schemes to achieve the for the case with two receivers and two eavesdroppers are constructed to demonstrate the necessity of a prefix channel in encoder design. Finally, the multi-antenna (i.e., MIMO compound wiretap channel is studied. The secrecy capacity is established for the degraded case and an achievable is given for the general case.

  11. Light metal compound casting

    Institute of Scientific and Technical Information of China (English)

    Konrad; J.; M.; PAPIS; Joerg; F.; LOEFFLER; Peter; J.; UGGOWITZER

    2009-01-01

    Compound casting’simplifies joining processes by directly casting a metallic melt onto a solid metal substrate. A continuously metallurgic transition is very important for industrial applications, such as joint structures of spaceframe constructions in transport industry. In this project, ‘compound casting’ of light metals is investigated, aiming at weight-saving. The substrate used is a wrought aluminium alloy of type AA5xxx, containing magnesium as main alloying element. The melts are aluminium alloys, containing various alloying elements (Cu, Si, Zn), and magnesium. By replacing the natural oxygen layer with a zinc layer, the inherent wetting difficulties were avoided, and compounds with flawless interfaces were successfully produced (no contraction defects, cracks or oxides). Electron microscopy and EDX investigations as well as optical micrographs of the interfacial areas revealed their continu- ously metallic constitution. Diffusion of alloying elements leads to heat-treatable microstructures in the vicinity of the joining interfaces in Al-Al couples. This permits significant variability of mechanical properties. Without significantly cutting down on wettability, the formation of low-melting intermetallic phases (Al3Mg2 and Al12Mg17 IMPs) at the interface of Al-Mg couples was avoided by applying a protective coating to the substrate.

  12. Light metal compound casting

    Institute of Scientific and Technical Information of China (English)

    Konrad J.M.PAPIS; Joerg F.LOEFFLER; Peter J.UGGOWITZER

    2009-01-01

    'Compound casting'simplifies joining processes by directly casting a metallic melt onto a solid metal substrate. A continuously metallurgic transition is very important for industrial applications, such as joint structures of spaceframe constructions in transport industry. In this project, 'compound casting' of light metals is investigated, aiming at weight-saving. The substrate used is a wrought aluminium alloy of type AA5xxx, containing magnesium as main alloying element. The melts are aluminium alloys, containing various alloying elements (Cu, Si, Zn), and magnesium. By replacing the natural oxygen layer with a zinc layer, the inherent wetting difficulties were avoided, and compounds with flawless interfaces were successfully produced (no contraction defects, cracks or oxides). Electron microscopy and EDX investigations as well as optical micrographs of the interfacial areas revealed their continu-ously metallic constitution. Diffusion of alloying elements leads to heat-treatable microstructures in the vicinity of the joining interfaces in Al-Al couples. This permits significant variability of mechanical properties. Without significantly cutting down on wettability, the formation of low-melting intermetallic phases (Al3Mg2 and AI12Mg17 IMPs) at the interface of Al-Mg couples was avoided by applying a protec-tive coating to the substrate.

  13. Toxic compounds in honey.

    Science.gov (United States)

    Islam, Md Nazmul; Khalil, Md Ibrahim; Islam, Md Asiful; Gan, Siew Hua

    2014-07-01

    There is a wealth of information about the nutritional and medicinal properties of honey. However, honey may contain compounds that may lead to toxicity. A compound not naturally present in honey, named 5-hydroxymethylfurfural (HMF), may be formed during the heating or preservation processes of honey. HMF has gained much interest, as it is commonly detected in honey samples, especially samples that have been stored for a long time. HMF is a compound that may be mutagenic, carcinogenic and cytotoxic. It has also been reported that honey can be contaminated with heavy metals such as lead, arsenic, mercury and cadmium. Honey produced from the nectar of Rhododendron ponticum contains alkaloids that can be poisonous to humans, while honey collected from Andromeda flowers contains grayanotoxins, which can cause paralysis of limbs in humans and eventually leads to death. In addition, Melicope ternata and Coriaria arborea from New Zealand produce toxic honey that can be fatal. There are reports that honey is not safe to be consumed when it is collected from Datura plants (from Mexico and Hungary), belladonna flowers and Hyoscamus niger plants (from Hungary), Serjania lethalis (from Brazil), Gelsemium sempervirens (from the American Southwest), Kalmia latifolia, Tripetalia paniculata and Ledum palustre. Although the symptoms of poisoning due to honey consumption may differ depending on the source of toxins, most common symptoms generally include dizziness, nausea, vomiting, convulsions, headache, palpitations or even death. It has been suggested that honey should not be considered a completely safe food. PMID:24214851

  14. Mineral protection of soil carbon counteracted by root exudates

    Science.gov (United States)

    Keiluweit, Marco; Bougoure, Jeremy J.; Nico, Peter S.; Pett-Ridge, Jennifer; Weber, Peter K.; Kleber, Markus

    2015-06-01

    Multiple lines of existing evidence suggest that climate change enhances root exudation of organic compounds into soils. Recent experimental studies show that increased exudate inputs may cause a net loss of soil carbon. This stimulation of microbial carbon mineralization (`priming’) is commonly rationalized by the assumption that exudates provide a readily bioavailable supply of energy for the decomposition of native soil carbon (co-metabolism). Here we show that an alternate mechanism can cause carbon loss of equal or greater magnitude. We find that a common root exudate, oxalic acid, promotes carbon loss by liberating organic compounds from protective associations with minerals. By enhancing microbial access to previously mineral-protected compounds, this indirect mechanism accelerated carbon loss more than simply increasing the supply of energetically more favourable substrates. Our results provide insights into the coupled biotic-abiotic mechanisms underlying the `priming’ phenomenon and challenge the assumption that mineral-associated carbon is protected from microbial cycling over millennial timescales.

  15. Morphology of uranium compounds

    International Nuclear Information System (INIS)

    Uranium metal is being used as nuclear fuel for Indian Research Reactors. During production of U metal various intermediate compounds of uranium are being processed. Physical, chemical properties of these compounds are important in overall processing rate and conversion determination. As no systematic data on morphology of these compounds were available, study was conducted to record the morphology of various U-compounds which are important in production of ceramic and metallic U-fuel for reactors. Most important intermediates were found to be ammonium diuranate (ADU) and uranium oxide (UO3/UO2). Morphology of these powders controls their flowability required for further material movement through different equipment, surface area required for chemical reactivity of powder, carryover losses occurred during gas solid counter current reaction and tap density required for effective capacity determination. ADU particle basically consists of primary platelets of 250-500 nm width and of 500-1000 nm length. These primary platelets form primary agglomerates. These agglomerates look like woollen balls or balls or cauliflower and primary agglomerates are also connected with each other to form secondary agglomerates. The basic morphology of ADU is maintained in UO3 even after calcination at high temperature. Pores are generated at the surface of platelet of UO3 due to release of gaseous reaction products during calcination. As temperature increases more pores are generated and sintering also starts. Specific surface area of UO3, produced by the calcination of ammonium di-urinate is generally a function of two competing processes: generation of surface area due to generation of pores because of the evolution of gaseous products (NH3, H2O vapour) and the loss of surfaces due to sintering. As a results surface area increases with calcination temperature due to generation of pores and then reduces. It has also been observed that morphology of the compounds are very much processing

  16. Calcium carbonate interaction analysis in polypropylene compounds and their impact on the formation of beta crystalline phase of this polymer; Analise da interacao de diferentes tipos de carbonato de calcio em compositos de polipropileno e suas consequencias na formacao da fase cristalina beta do PP

    Energy Technology Data Exchange (ETDEWEB)

    NONE

    2011-07-01

    The insertion of calcium carbonate (CaCO{sub 3}) in polypropylene compound is a thoroughly known technique widely studied in the academic area and in the industry. Its wide application is due, mainly, to increase mechanical properties with low manufacturing cost. These improvements in this polymer make it more versatile and competitive compared to other expensive polymers. In this study, the incorporation of four types of CaCO3 from the same manufacturer were compared and the focus was on the size of this mineral filler. Furthermore, it was analyzed the interaction of graphitized polypropylene with maleic anhydride (PP-g-MA) in the same samples. All these samples were analyzed by WAXS and SEM. The physical properties of tensile strength and impact were also analyzed. It was observed from this study that the smallest CaCO3 produced with PP-g-MA resulted in better physical properties with the formation of a crystalline phase beta, as originally studied by other authors using other raw materials. (author)

  17. Xenobiotic organic compounds in wastewater

    DEFF Research Database (Denmark)

    Eriksson, Eva; Baun, Anders; Henze, Mogens; Ledin, Anna

    Information regarding the contents of xenobiotic organic compounds (XOCs) in wastewater is limited, but it has been shown that at least 900 different compounds / compound groups could potentially be present in grey wastewater. Analyses of Danish grey wastewater revealed the presence of several...... hundred of XOCs, among them mainly originating from hygiene products: chlorophenols, detergents and phthalates. Several compounds not deriving from hygiene products were also identified e.g. flame-retardants and drugs. A environmental hazard identification showed that a large number of compounds with high...... aquatic toxicity were present and that data for environmental fate could only be retrieved for about half of the compounds....

  18. Nomenclature on an inorganic compound

    International Nuclear Information System (INIS)

    This book contains eleven chapters : which mention nomenclature of an inorganic compound with introduction and general principle on nomenclature of compound. It gives the description of grammar for nomenclature such as brackets, diagonal line, asterisk, and affix, element, atom and groups of atom, chemical formula, naming by stoichiometry, solid, neutral molecule compound, ion, a substituent, radical and name of salt, oxo acid and anion on introduction and definition of oxo acid, coordination compound like symbol of stereochemistry , boron and hydrogen compound and related compound.

  19. Xenobiotic organic compounds in wastewater

    DEFF Research Database (Denmark)

    Eriksson, Eva; Baun, Anders; Henze, Mogens;

    2002-01-01

    Information regarding the contents of xenobiotic organic compounds (XOCs) in wastewater is limited, but it has been shown that at least 900 different compounds / compound groups could potentially be present in grey wastewater. Analyses of Danish grey wastewater revealed the presence of several...... hundred of XOCs, among them mainly originating from hygiene products: chlorophenols, detergents and phthalates. Several compounds not deriving from hygiene products were also identified e.g. flame-retardants and drugs. A environmental hazard identification showed that a large number of compounds with high...... aquatic toxicity were present and that data for environmental fate could only be retrieved for about half of the compounds....

  20. Synthesis and Characterization of MWCNT/ CaCO3 Hybrid Compound

    International Nuclear Information System (INIS)

    Since their discovery, carbon nano tubes (CNT) have been actively researched and drawn a great interest for a wide variety of potential application. Several of synthesis method have been developed for the production of CNT. In this work, the chemical vapor deposition (CVD) technique was used to synthesis the multi walled carbon nano tubes/ calcium carbonate (MWCNT/ CaCO3) hybrid compound. A gas mixture of CH4/ N2 was used as the source of carbon and Ni/ CaCO3 compound was used as catalyst for the growth of the hybrid compound. The catalyst was prepared using nickel salt and CaCO3 mixture via coprecipitation method. The process was then followed by drying, calcination, reduction and growth the CNT in the tube furnace. The resulted compound was then analysed using XRD, SEM and HRTEM. (author)

  1. Correlation between the structure and infra-red absorption characteristics of mono-deuterated compounds: contribution to the study of organo-magnesium compounds

    International Nuclear Information System (INIS)

    The high sensitivity of the ν (C-D) vibration to the variations brought about by the substitution of the carbon attached to the deuterium is shown in the case of organic or organo-metallic mono-deuterated molecules. In particular, syntheses of various mono-deuterated organo-magnesium compounds have been carried out; results are given concerning an infra-red spectrometric examination of these compounds in the range 2100 - 2250 cm-1. The results show the existence of only one type of deuterated carbon, which suggests that the same carbanion is involved in various ionic associations for the different magnesium-containing compounds. (authors)

  2. Highly Efficient Oxidative Cleavage of Carbon-Carbon Double Bond over meso-Tetraphenyl Cobalt Porphyrin Catalyst in the Presence of Molecular Oxygen

    Institute of Scientific and Technical Information of China (English)

    周贤太; 纪红兵

    2012-01-01

    Highly efficient and selective carbon-carbon double bond aerobic cleavage of olefins catalyzed by metallopor- phyrins was investigated, and carbonyl compounds and epoxide were produced as the main products. CoTPP (co- balt meso-tetraphenyl porphyrin) showed excellent activity for the oxidative cleavage of carbon-carbon double bond by using styrene as model compound, in which the TOF (turnover frequency) and selectivity toward benzaldehyde was obtained with 2×10^4h-1 and 86%,respectively.

  3. Offset Compound Gear Drive

    Science.gov (United States)

    Stevens, Mark A.; Handschuh, Robert F.; Lewicki, David G.

    2010-01-01

    The Offset Compound Gear Drive is an in-line, discrete, two-speed device utilizing a special offset compound gear that has both an internal tooth configuration on the input end and external tooth configuration on the output end, thus allowing it to mesh in series, simultaneously, with both a smaller external tooth input gear and a larger internal tooth output gear. This unique geometry and offset axis permits the compound gear to mesh with the smaller diameter input gear and the larger diameter output gear, both of which are on the same central, or primary, centerline. This configuration results in a compact in-line reduction gear set consisting of fewer gears and bearings than a conventional planetary gear train. Switching between the two output ratios is accomplished through a main control clutch and sprag. Power flow to the above is transmitted through concentric power paths. Low-speed operation is accomplished in two meshes. For the purpose of illustrating the low-speed output operation, the following example pitch diameters are given. A 5.0 pitch diameter (PD) input gear to 7.50 PD (internal tooth) intermediate gear (0.667 reduction mesh), and a 7.50 PD (external tooth) intermediate gear to a 10.00 PD output gear (0.750 reduction mesh). Note that it is not required that the intermediate gears on the offset axis be of the same diameter. For this example, the resultant low-speed ratio is 2:1 (output speed = 0.500; product of stage one 0.667 reduction and stage two 0.750 stage reduction). The design is not restricted to the example pitch diameters, or output ratio. From the output gear, power is transmitted through a hollow drive shaft, which, in turn, drives a sprag during which time the main clutch is disengaged.

  4. Application of Cycloaddition Reactions to the Syntheses of Novel Boron Compounds

    OpenAIRE

    John A. Maguire; Hosmane, Narayan S; Yinghuai Zhu; Xiao Siwei

    2010-01-01

    This review covers the application of cycloaddition reactions in forming the boron-containing compounds such as symmetric star-shaped boron-enriched dendritic molecules, nano-structured boron materials and aromatic boronic esters. The resulting boron compounds are potentially important reagents for both materials science and medical applications such as in boron neutron capture therapy (BNCT) in cancer treatment and as drug delivery agents and synthetic intermediates for carbon-carbon cross-c...

  5. New compounds as potential radio diagnosticians Alzheimer

    International Nuclear Information System (INIS)

    Alzheimer's disease (AD) is the most common cause of dementia in Cuba and all over the World. According to demographic trends it has been called the epidemic of the century. It is characterized by the presence of neuropathological brain deposits: senile plaques, formed by neurofibrillary tangles (NT) and deposits of β-amyloid protein (Aß). Aß plaques could appear even 20 years before the establishment of first clinical symptoms of the disease. The aim of this study was to synthesize new naphthalene derivatives, feasible to be labeled with radionuclides emitters of either gamma radiation or positrons. These labeled compounds should be able to cross blood–brain barrier (BBB) in healthy and AD transgenic animals. As a result of this work, several synthetic precursors were synthesized, which were labeled with iodine-131, carbon-11 and fluorine-18 with a satisfactory radiochemical purity. The corresponding non-radioactive control compounds were also synthesized.In in vitro and in silico studies, obtained compounds showed affinity for the β-amyloid protein. According to SPECT and PET-CT images in healthy laboratory animals, obtained labeled compounds crossed BBB in a bi-directional way without any sign of brain uptake.Furthermore, evaluation of the biodistribution of the [18F] -2- (3-fluoropropyl) -6-methoxynaphthalene ([[18F] Amyloid® was performed in healthy animals.[[18F]Amylovis crossed blood brain barrier. Renal and hepatic pathways were the main excretion routes. On the other hand, in transgenic mice with AD, its uptake and its retention time were higher in comparison with healthy mice. Immunohistochemistry and Congo red staining of control and transgenic mice brain slices were performed to identify β-amyloid plaques.Conclusions: Obtained compounds were able to bi-directionally cross BBB.[[18F]Amylovis® could be a promising PET radiotracer for amyloid plaques visualization. (author)

  6. Compound semiconductor integrated circuits

    CERN Document Server

    Vu, Tho T

    2003-01-01

    This is the book version of a special issue of the International Journal of High Speed Electronics and Systems , reviewing recent work in the field of compound semiconductor integrated circuits. There are fourteen invited papers covering a wide range of applications, frequencies and materials. These papers deal with digital, analog, microwave and millimeter-wave technologies, devices and integrated circuits for wireline fiber-optic lightwave transmissions, and wireless radio-frequency microwave and millimeter-wave communications. In each case, the market is young and experiencing rapid growth

  7. Titanium alkoxide compound

    Science.gov (United States)

    Boyle, Timothy J.

    2007-08-14

    A titanium alkoxide composition is provided, as represented by the chemical formula (OC.sub.6H.sub.5N).sub.2Ti(OC.sub.6H.sub.5NH.sub.2).sub.2. As prepared, the compound is a crystalline substance with a hexavalent titanium atom bonded to two OC.sub.6H.sub.5NH.sub.2 groups and two OC.sub.6H.sub.5N groups with a theoretical molecular weight of 480.38, comprising 60.01% C, 5.04% H and 11.66% N.

  8. Building carbon–carbon bonds using a biocatalytic methanol condensation cycle

    OpenAIRE

    Bogorad, Igor W.; Chen, Chang-Ting; Theisen, Matthew K.; Wu, Tung-Yun; Schlenz, Alicia R.; Lam, Albert T.; Liao, James C.

    2014-01-01

    With the recent discoveries of large reserves of natural gas, the efficient utilization of one-carbon compounds for chemical synthesis would reduce the raw material cost for the petroleum-based chemical industry. Methanol is produced industrially from methane and is a feedstock chemical for the synthesis of higher carbon compounds. However, current chemical synthesis of higher carbon compounds from methanol requires high temperature and pressure. Natural biological pathways for methanol utili...

  9. Improvement in char formability of phenolic resin for development of Carbon/Carbon composites

    International Nuclear Information System (INIS)

    In the processing of carbon/carbon composites using polymer resin as the matrix precursor, it is inevitable that a porous structure was formed after carbonization. As a result, densification by liquid phase impregnation followed by recarbonization is required to obtain a densified composite. Consequently, the char formability of resin is an important factor in reducing the number of densification cycles and hence the processing cost. In this study, a novel approach is adopted to improve the densification of carbon/carbon composites by using a new phenolic resin modified by pitch. For this purpose, soluble part of pitch was extracted and dispersed in resol type phenolic resin. The polymerization reaction was performed in presence of para-formaldehyde and a resol-pitch compound was obtained. The second compound was prepared by mixing novolac-furfural in 55:45 weight ratio containing 9% by weight hexamethylene tetramine. This compound was added to resol-pitch compound in 10,20,50 and 80 w %. The microstructure of carbonized resin was investigated by X-ray diffraction and char yield, and the linear and volumetric shrinkage were obtained. Results show that in 80:20 ratio of resol-pitch to novolac-furfural , the char yield would be maximized by 71% and volumetric shrinkage would be minimized at 16.4%. At the same time, XRD results indicate that the resin has a strong ability to graphitize carbon/carbon composites matrix as a necessary step for its processing

  10. New carbon-carbon linked amphiphilic carboranyl-porphyrins as boron neutron capture agents

    International Nuclear Information System (INIS)

    Novel amphiphilic carboranyl-porphyrins have been synthesized for Boron Neutron Capture Therapy (BNCT). These compounds have carbon-carbon bonds between the carborane residues and the porphyrin meso-phenyl groups, and contain 28-31% boron by weight . (author)

  11. Catalytic properties of niobium compounds

    International Nuclear Information System (INIS)

    The catalytic activity and selectivity of niobium compounds including oxides, salts, organometallic compounds and others are outlined. The application of these compounds as catalysts to diversified reactions is reported. The nature and action of niobium catalysts are characteristic and sometimes anomalous, suggesting the necessity of basic research and the potential use as catalysts for important processes in the chemical industry. (Author)

  12. Goldenphilicity: Luminescent gold compounds

    International Nuclear Information System (INIS)

    In the solids and molecules different types of bonds are presented depending on the involved atoms, covalent bonds are common among elements of open shell, where more bond orbitals are filled than anti bond orbitals. It is expected that ionic bonds among closed shell atoms which have charges of opposite sign. Bonds type Van der Waals are presented among molecules which have a bipolar moment. It would not be expected bonds among zero charge species, or more generally with the same nominal charge and in any case the attractive forces would be very small. In fact it is expected that two metallic cations to be repelled each other. There recently is evidence that in organic or organometallic compounds could exist attractive interactions between two cations of the d8 -d10 -s2 families. These bonds are weak but stronger than those of Van der Waals. They are compared with the hydrogen bonds. In this work it was reviewed some examples in which the goldenphilicity plays an important role in the luminescence that the gold complexes present. Examples of mono, bi and trinuclear and the structures that these organometallic compounds could take are examined. (Author)

  13. Drought-induced carbon loss in peatlands

    Science.gov (United States)

    Fenner, Nathalie; Freeman, Chris

    2011-12-01

    Peatlands store vast amounts of organic carbon, amounting to approximately 455 Pg. Carbon builds up in these water-saturated environments owing to the presence of phenolic compounds--which inhibit microbial activity and therefore prevent the breakdown of organic matter. Anoxic conditions limit the activity of phenol oxidase, the enzyme responsible for the breakdown of phenolic compounds. Droughts introduce oxygen into these systems, and the frequency of these events is rising. Here, we combine in vitro manipulations, mesocosm experiments and field observations to examine the impact of drought on peatland carbon loss. We show that drought stimulates bacterial growth and phenol oxidase activity, resulting in a reduction in the concentration of phenolic compounds in peat. This further stimulates microbial growth, causing the breakdown of organic matter and the release of carbon dioxide in a biogeochemical cascade. We further show that re-wetting the peat accelerates carbon losses to the atmosphere and receiving waters, owing to drought-induced increases in nutrient and labile carbon levels, which raise pH and stimulate anaerobic decomposition. We suggest that severe drought, and subsequent re-wetting, could destabilize peatland carbon stocks; understanding this process could aid understanding of interactions between peatlands and other environmental trends, and lead to the development of strategies for increasing carbon stocks.

  14. Organic chemistry of Murchison meteorite: Carbon isotopic fractionation

    Science.gov (United States)

    Yuen, G. U.; Blair, N. E.; Desmarais, D. J.; Cronin, J. R.; Chang, S.

    1986-01-01

    The carbon isotopic composition of individual organic compounds of meteoritic origin remains unknown, as most reported carbon isotopic ratios are for bulk carbon or solvent extractable fractions. The researchers managed to determine the carbon isotopic ratios for individual hydrocarbons and monocarboxylic acids isolated from a Murchison sample by a freeze-thaw-ultrasonication technique. The abundances of monocarboxylic acids and saturated hydrocarbons decreased with increasing carbon number and the acids are more abundant than the hydrocarbon with the same carbon number. For both classes of compounds, the C-13 to C-12 ratios decreased with increasing carbon number in a roughly parallel manner, and each carboxylic acid exhibits a higher isotopic number than the hydrocarbon containing the same number of carbon atoms. These trends are consistent with a kinetically controlled synthesis of higher homologues for lower ones.

  15. Magnetic Carbon Supported Palladium Nanoparticles: An Efficient and Sustainable Catalyst for Hydrogenation Reactions

    Science.gov (United States)

    Magnetic carbon supported Pd catalyst has been synthesized via in situ generation of nanoferrites and incorporation of carbon from renewable cellulose via calcination; the catalyst can be used for the hydrogenation of alkenes and reduction of aryl nitro compounds.

  16. Semiconducting III-V compounds

    CERN Document Server

    Hilsum, C; Henisch, Heinz R

    1961-01-01

    Semiconducting III-V Compounds deals with the properties of III-V compounds as a family of semiconducting crystals and relates these compounds to the monatomic semiconductors silicon and germanium. Emphasis is placed on physical processes that are peculiar to III-V compounds, particularly those that combine boron, aluminum, gallium, and indium with phosphorus, arsenic, and antimony (for example, indium antimonide, indium arsenide, gallium antimonide, and gallium arsenide).Comprised of eight chapters, this book begins with an assessment of the crystal structure and binding of III-V compounds, f

  17. 77 FR 14324 - National Volatile Organic Compound Emission Standards for Aerosol Coatings-Addition of Dimethyl...

    Science.gov (United States)

    2012-03-09

    ...The EPA is proposing to amend the National Volatile Organic Compound Emission Standards for Aerosol Coatings final rule, which is a rule that establishes national reactivity-based emission standards for the aerosol coatings category (aerosol spray paints) under the Clean Air Act. This proposed action adds three compounds: dimethyl carbonate, benzotrifluoride, and hexamethyldisiloxane and their......

  18. Adsorption of gases on a surface of A3B5 compounds of the indium group

    International Nuclear Information System (INIS)

    Adsorption properties of semiconducting compounds InB5 (B5 = P, As, Sb) relative to hydrogen and carbon dioxide by their individual and mutual manifestations are studied with application of the complex of modern methods. The nature of active centres and surface compounds, mechanism and regularities of processes are established

  19. Natural Biodegradation of Phenolic Compounds in Groundwater

    Institute of Scientific and Technical Information of China (English)

    2000-01-01

    A combination of field data and theoretical approaches is used to assess the natural attenuation and status of a complex plume of phenolic compounds (phenol, cresols, xylenols) in a deep, consolidated, UK Permo-Triassic sandstone aquifer. Biodegradation of the phenolic compounds at concentrations up to 12500mg·L-1 is occurring under aerobic, NO-3-reducing, Mn/Fe-reducing, SO2-4-reducing and methanogenic conditions in the aquifer, with the accumulation of inorganic and organic metabolites in the plume. An electron and carbon balance for the plume suggests that only 6% of the source term has been degraded in 50 years. The residual contaminant mass in the plume significantly exceeds estimates of electron acceptor inputs, indicating that the plume will grow. Two detailed vertical profiles through the plume show that contaminant distributions are controlled more by source history than by biodegradation processes. Microbiological and mass balance studies show that biodegradation is greatest at the plume fringe where contaminant concentrations are diluted by transverse mixing. Active bacterial populations exist throughout the plume but biodegradation is inhibited in the plume core by high contaminant concentrations. Stable isotope studies show that SO2-4-reduction is particularly sensitive to contaminant concentration. The aquifer is not oxidant-deficient but natural attenuation of the phenolic compounds in this system is limited by toxicity from the pollutant load and the bioavailability of electron acceptors. Natural attenuation of these contaminants will increase only after increased dilution of the plume.

  20. "Hello, I'm Carbon.": Writing about Elements and Compounds

    Science.gov (United States)

    Stout, Roland P.

    2010-01-01

    General chemistry students are asked to assume the identity of an element and to write their own story. In the spirit of pedagogical approaches such as writing-to-learn and writing across the curriculum, this assignment has several objectives, most significantly to connect students to the discipline of chemistry in a robust way. Facilitating this…

  1. Genetics of Bacteria That Oxidize On-Carbon Compounds

    Energy Technology Data Exchange (ETDEWEB)

    Hanson, Richard S.

    2001-01-01

    Facultative methanol oxidizing bacteria contain large amounts of methanol dehydrogenase which is expressed only in the presence of methanol. This technical report describes two-two component regulatory systems encoding histidine kinases and response regulators and another response regulator all of which are required for the expression of mxaF, the open reading frame encoding methanol dehydrogenase. The response regulators bind to sequences upstream of the mxaF when phosphoryled in a reaction catalyzed by the histidine kinases. The binding of the response regulators is required for the transcription of mxaF.

  2. Carbon Particles and Organic Compounds in Hard Coal Waste

    Czech Academy of Sciences Publication Activity Database

    Sýkorová, Ivana; Havelcová, Martina; Klika, Z.; Trejtnarová, Hana; Fojtíková, M.; Martinec, Petr; Šulc, Alexandr

    Freiberg: TU Bergakademie Freiberg, 2010, s. 418-419. ISBN 978-3-86012-397-3. [Second International Conference on Coal Fire Research ICCFR2. Berlin (DE), 19.05.2010-21.05.2010] R&D Projects: GA AV ČR IAA300460804 Institutional research plan: CEZ:AV0Z30460519; CEZ:AV0Z30860518 Keywords : coal waste s * organic matter * PAHs Subject RIV: DM - Solid Waste and Recycling

  3. An Impact of Biofield Treatment on Spectroscopic Characterization of Pharmaceutical Compounds

    OpenAIRE

    Trivedi, Mahendra

    2015-01-01

    The stability of any pharmaceutical compound is most desired quality that determines its shelf life and effectiveness. The stability can be correlated to structural and bonding properties of compound and any variation arise in these properties can be easily determined by spectroscopic analysis. The present study was aimed to evaluate the impact of biofield treatment on these properties of four pharmaceutical compounds such as urea, thiourea, sodium carbonate, and magnesium sulphate, using spe...

  4. An Impact of Biofield Treatment on Spectroscopic Characterization of Pharmaceutical Compounds

    OpenAIRE

    Trivedi, Mahendra Kumar

    2015-01-01

    The stability of any pharmaceutical compound is most desired quality that determines its shelf life and effectiveness.The stability can be correlated to structural and bonding properties of compound and any variation arise in these properties can be easily determined by spectroscopic analysis. The present study was aimed to evaluate the impact of biofield treatment on these properties of four pharmaceutical compounds such as urea, thiourea, sodium carbonate,and magnesium sulphate, using spect...

  5. Volatile organic compounds

    International Nuclear Information System (INIS)

    The goal is: Not more emission of volatile organic compounds (VOCs) than necessary. The items discussed in this presentation are the VOCs, how to calculate emission of VOCs, how to reduce or avoid them, and different recovery processes. The largest source of Norwegian emissions of non methane VOCs (NMVOCs) is offshore loading of raw petroleum. Emissions of VOCs should be reduced mainly for two reasons: (1) on sunny days NMVOCs may react with NOx to form ozon and smog close to the surface, (2) ozone and smog close to the surface may be harmful to plants and animals, and they are hazardous to human health. As for the calculation of VOC emissions, the VOCON project will release the calculation program HCGASS in 1999. This project is a cooperative project headed by SINTEF/Marintek

  6. Microoptical telescope compound eye.

    Science.gov (United States)

    Duparré, Jacques; Schreiber, Peter; Matthes, André; Pshenay-Severin, Ekaterina; Bräuer, Andreas; Tünnermann, Andreas; Völkel, Reinhard; Eisner, Martin; Scharf, Toralf

    2005-02-01

    A new optical concept for compact digital image acquisition devices with large field of view is developed and proofed experimentally. Archetypes for the imaging system are compound eyes of small insects and the Gabor-Superlens. A paraxial 3x3 matrix formalism is used to describe the telescope arrangement of three microlens arrays with different pitch to find first order parameters of the imaging system. A 2mm thin imaging system with 21x3 channels, 70 masculinex10 masculine field of view and 4.5mm x 0.5mm image size is optimized and analyzed using sequential and non-sequential raytracing and fabricated by microoptics technology. Anamorphic lenses, where the parameters are a function of the considered optical channel, are used to achieve a homogeneous optical performance over the whole field of view. Captured images are presented and compared to simulation results. PMID:19494951

  7. ST Elevation Myocardial Infarction Due to Carbon Monoxide Poisoning

    OpenAIRE

    2011-01-01

    Carbon monoxide is formed as a result of combustion of any carbon compound and can lead to hypoxia in many organs including the brain and the heart. Carbon monoxide poisoning in the United States is the leading cause of the fatal poisonings. In this study we present a case with no-known accompanying disease in the light of literature where myocardial infarction was developed as a result of carbon monoxide poisoning.

  8. Zirconium sulfate interaction with sodium carbonate in solution

    International Nuclear Information System (INIS)

    Zirconium sulfate interaction with sodium carbonate is studied in aqueous solution. By pH-metry and infrared spectroscopy it is stated that depending on the carbonate concentration Zr(OH)2x(CO3)22-, ZrOH(CO3)33- and Zr(CO3)44- compounds can be formed in sulfatocarbonate solutions. pH range in which soluble carbonate complexes exist also depends on the concentration of sodium carbonate. Calculated is the fourth stability constant

  9. ST Elevation Myocardial Infarction Due to Carbon Monoxide Poisoning

    Directory of Open Access Journals (Sweden)

    Hayriye Gonullu

    2011-08-01

    Full Text Available Carbon monoxide is formed as a result of combustion of any carbon compound and can lead to hypoxia in many organs including the brain and the heart. Carbon monoxide poisoning in the United States is the leading cause of the fatal poisonings. In this study we present a case with no-known accompanying disease in the light of literature where myocardial infarction was developed as a result of carbon monoxide poisoning.

  10. Organic compounds in meteorites and their origins

    Science.gov (United States)

    Hayatsu, R.; Anders, E.

    1981-01-01

    The current investigation represents an extensively updated version of a review conducted by Anders et al. (1973). The investigation takes into account the literature through mid-1980. It is pointed out that Type 1 carbonaceous chondrites (C1) contain 6% of their cosmic complement of carbon, mainly in the form of organic matter. Most authors now agree that this material represents primitive prebiotic matter. The principal questions remaining are what abiotic processes formed the organic matter, and to what extent these processes took place in locales other than the solar nebula, such as interstellar clouds or meteorite parent bodes. The problem is approached in three stages. It is attempted to reconstruct the physical conditions during condensation from the clues contained in the inorganic matrix of the meteorite. The condensation behavior of carbon under these conditions is determined on the basis of thermodynamic calculations. Model experiments on the condensation of carbon are performed, and the synthesized compounds are compared with those actually found in meteorites.

  11. Carbon nanotube- and carbon fiber-reinforcement of ethylene-octene copolymer membranes for gas and vapor separation

    OpenAIRE

    Zuzana Sedláková; Gabriele Clarizia; Paola Bernardo; Johannes Carolus Jansen; Petr Slobodian; Petr Svoboda; Magda Kárászová; Karel Friess; Pavel Izak

    2014-01-01

    Gas and vapor transport properties were studied in mixed matrix membranes containing elastomeric ethylene-octene copolymer (EOC or poly(ethylene-co-octene)) with three types of carbon fillers: virgin or oxidized multi-walled carbon nanotubes (CNTs) and carbon fibers (CFs). Helium, hydrogen, nitrogen, oxygen, methane, and carbon dioxide were used for gas permeation rate measurements. Vapor transport properties were studied for the aliphatic hydrocarbon (hexane), aromatic compound (toluene), al...

  12. Porous carbons

    Indian Academy of Sciences (India)

    Satish M Manocha

    2003-02-01

    Carbon in dense as well as porous solid form is used in a variety of applications. Activated porous carbons are made through pyrolysis and activation of carbonaceous natural as well as synthetic precursors. Pyrolysed woods replicate the structure of original wood but as such possess very low surface areas and poor adsorption capacities. On activation, these exhibit increased adsorption volumes of 0.5–0.8 cm3 /gm and surface areas of 700–1800 m2 /gm depending on activation conditions, whether physical or chemical. Former carbons possess mixed pore size distribution while chemically activated carbons predominantly possess micropores. Thus, these carbons can be used for adsorption of wide distributions of molecules from gas to liquid. The molecular adsorption within the pores is due to single layer or multilayer molecule deposition at the pore walls and hence results in different types of adsorption isotherm. On the other hand, activated carbon fibres with controlled microporous structure and surface area in the range of 2500 m2 /gm can be developed by controlled pyrolysis and physical activation of amorphous carbon fibres. Active carbon fibres with unmatchable pore structure and surface characteristics are present and futuristic porous materials for a number of applications from pollution control to energy storage.

  13. Biodegradation of munitions compounds by a sulfate reducing bacterial enrichment culture

    Energy Technology Data Exchange (ETDEWEB)

    Boopathy, R.; Manning, J. [Argonne National Lab., IL (United States). Environmental Research Div.

    1997-08-01

    The degradation of several munitions compounds was studied. The compounds included 2,4,6-trinitrotoluene (TNT), hexahydro-1,3,5-trinitro-1,3,5-triazine, octahydro-1,3,5,7-tetranitro-1,3,5,7-tetraazocine, 2,4,6-trinitrobenzene (TNB), and 2,4-dinitrotoluene. All of the compounds studied were degraded by the sulfate reducing bacterial (SRB) enrichment culture. The SRB culture did not use the munitions compounds as their sole source of carbon. However, all the munitions compounds tested served as the sole source of nitrogen for the SRB culture. Degradation of munitions compounds was achieved by a co-metabolic process. The SRB culture used a variety of carbon sources including pyruvate, ethanol, formate, lactate, and H{sub 2}-CO{sub 2}. The SRB culture was an incomplete oxidizer, unable to carry out the terminal oxidation of organic substrates to CO{sub 2} as the sole product, and it did not use acetate or methanol as a carbon source. In addition to serving as nitrogen sources, the munitions compounds also served as electron acceptors in the absence of sulfate. A soil slurry experiment with 5% and 10% munitions compounds-contaminated soil showed that the contaminant TNT was metabolized by the SRB culture in the presence of pyruvate as electron donor. This culture may be useful in decontaminating munitions compounds-contaminated soil and water under anaerobic conditions.

  14. Activation of diboron reagents: The development of mild conditions for the synthesis of unique organoboron compounds

    OpenAIRE

    Thorpe, Steven Brandon

    2012-01-01

    The first successful synthesis and isolation of a boronic acid was reported in 1860 by Frankland in the pursuit of novel organometallic compounds. For more than a century, further studies of boronic acids were sparsely published. Suzuki and Miyaura jumpstarted the field in 1979 with an innovative carbon-carbon bond forming reaction employing an organoboronic acid and a carbon halide under palladium catalysis. Indeed, the Nobel Prize in Chemistry was awarded to Professor Akira Suzuki, along wi...

  15. Application of Cycloaddition Reactions to the Syntheses of Novel Boron Compounds

    Directory of Open Access Journals (Sweden)

    John A. Maguire

    2010-12-01

    Full Text Available This review covers the application of cycloaddition reactions in forming the boron-containing compounds such as symmetric star-shaped boron-enriched dendritic molecules, nano-structured boron materials and aromatic boronic esters. The resulting boron compounds are potentially important reagents for both materials science and medical applications such as in boron neutron capture therapy (BNCT in cancer treatment and as drug delivery agents and synthetic intermediates for carbon-carbon cross-coupling reactions. In addition, the use of boron cage compounds in a number of cycloaddition reactions to synthesize unique aromatic species will be reviewed briefly.

  16. TSTA compound cryopump

    International Nuclear Information System (INIS)

    The Tritium System Test Assembly (TSTA), at the Los Alamos Scientific Laboratory, is intended to demonstrate realistic fuel supply and cleanup scenarios for future fusion reactors. The vacuum pumps must be capable of handling large quantities of reactor exhaust gases consisting largely of mixtures of hydrogen and helium isotopes. Cryocondensing pumps will not pump helium at 4.2 K; while cryosorption pumps using molecular sieves or charcoal have good helium pumping speed, the adsorbent clogs with condensed hydrogen while pumping mixtures of both. A solution to this problem is a compound design whereby the first stage condenses the hydrogen and the second, or sorption, stage pumps the helium. The TSTA pump designed at Lawrence Livermore National Laboratory uses argon gas to cryotrap the helium in the helium-hydrogen mixture. The argon is sprayed directly onto the 4.2 K surface at a rate proportional to the helium flow rate, permitting continuous pumping of the helium-hydrogen mixtures in a single-stage pump. However, the possibility of differential desorption as a first stage in the TSTA gas separation cycle required the inclusion of a first-stage hydrogen isotope condenser. The design, performance, and operating characteristics are discussed

  17. Compounding in synthetic aperture imaging.

    Science.gov (United States)

    Hansen, Jens Munk; Jensen, Jørgen Arendt

    2012-09-01

    A method for obtaining compound images using synthetic aperture data is investigated using a convex array transducer. The new approach allows spatial compounding to be performed for any number of angles without reducing the frame rate or temporal resolution. This important feature is an intrinsic property of how the compound images are constructed using synthetic aperture data and an improvement compared with how spatial compounding is obtained using conventional methods. The synthetic aperture compound images are created by exploiting the linearity of delay-and-sum beamformation for data collected from multiple spherical emissions to synthesize multiple transmit and receive apertures, corresponding to imaging the tissue from multiple directions. The many images are added incoherently, to produce a single compound image. Using a 192-element, 3.5-MHz, λ-pitch transducer, it is demonstrated from tissue-phantom measurements that the speckle is reduced and the contrast resolution improved when applying synthetic aperture compound imaging. At a depth of 4 cm, the size of the synthesized apertures is optimized for lesion detection based on the speckle information density. This is a performance measure for tissue contrast resolution which quantifies the tradeoff between resolution loss and speckle reduction. The speckle information density is improved by 25% when comparing synthetic aperture compounding to a similar setup for compounding using dynamic receive focusing. The cystic resolution and clutter levels are measured using a wire phantom setup and compared with conventional application of the array, as well as to synthetic aperture imaging without compounding. If the full aperture is used for synthetic aperture compounding, the cystic resolution is improved by 41% compared with conventional imaging, and is at least as good as what can be obtained using synthetic aperture imaging without compounding. PMID:23007781

  18. Biogenic volatile organic compounds - small is beautiful

    Science.gov (United States)

    Owen, S. M.; Asensio, D.; Li, Q.; Penuelas, J.

    2012-12-01

    While canopy and regional scale flux measurements of biogenic volatile organic compounds (bVOCs) are essential to obtain an integrated picture of total compound reaching the atmosphere, many fascinating and important emission details are waiting to be discovered at smaller scales, in different ecological and functional compartments. We concentrate on bVOCs below ground to pollination of flowers. Although bVOC emissions from soil surfaces are small, bVOCs are exuded by roots of some plant species, and can be extracted from decaying litter. Naturally occurring monoterpenes in the rhizosphere provide a specialised carbon source for micro-organisms, helping to define the micro-organism community structure, and impacting on nutrient cycles which are partly controlled by microorganisms. Naturally occurring monoterpenes in the soil system could also affect the aboveground structure of ecosystems because of their role in plant defence strategies and as mediating chemicals in allelopathy. A gradient of monoterpene concentration was found in soil around Pinus sylvestris and Pinus halepensis, decreasing with distance from the tree. Some compounds (α-pinene, sabinene, humulene and caryophyllene) in mineral soil were linearly correlated with the total amount of each compound in the overlying litter, indicating that litter might be the dominant source of these compounds. However, α-pinene did not fall within the correlation, indicating a source other than litter, probably root exudates. We also show that rhizosphere bVOCs can be a carbon source for soil microbes. In a horizontal gradient from Populus tremula trees, microbes closest to the tree trunk were better enzymatically equipped to metabolise labeled monoterpene substrate. Monoterpenes can also increase the degradation rate in soil of the persistant organic pollutants, likely acting as analogues for the cometabo-lism of polychlorinated biphenyls (PCBs) Flowers of a ginger species (Alpinia kwangsiensis) and a fig species

  19. Carbon speciation and surface tension of fog

    Science.gov (United States)

    Capel, P.D.; Gunde, R.; Zurcher, F.; Giger, W.

    1990-01-01

    The speciation of carbon (dissolved/particulate, organic/inorganic) and surface tension of a number of radiation fogs from the urban area of Zurich, Switzerland, were measured. The carbon species were dominated by "dissolved" organic carbon (DOC; i.e., the fraction that passes through a filter), which was typically present at levels of 40-200 mg/L. Less than 10% of the DOC was identified as specific individual organic compounds. Particulate organic carbon (POC) accounted for 26-41% of the mass of the particles, but usually less than 10% of the total organic carbon mass. Inorganic carbon species were relatively minor. The surface tensions of all the measured samples were less than pure water and were correlated with their DOC concentrations. The combination of high DOC and POC and low surface tension suggests a mechanism for the concentration of hydrophobic organic contaminants in the fog droplet, which have been observed by numerous investigators. ?? 1990 American Chemical Society.

  20. Deciphering ocean carbon in a changing world

    OpenAIRE

    Moran, Mary Ann; Kujawinski, Elizabeth B.; Stubbins, Aron; Fatland, Rob; Aluwihare, Lihini I.; Buchan, Alison; Crump, Byron C.; Dorrestein, Pieter C.; Dyhrman, Sonya T.; Hess, Nancy J.; Howe, Bill; Longnecker, Krista; Medeiros, Patricia M.; Niggemann, Jutta; Obernosterer, Ingrid

    2016-01-01

    Dissolved organic matter (DOM) in the oceans is one of the largest pools of reduced carbon on Earth, comparable in size to the atmospheric CO2 reservoir. A vast number of compounds are present in DOM, and they play important roles in all major element cycles, contribute to the storage of atmospheric CO2 in the ocean, support marine ecosystems, and facilitate interactions between organisms. At the heart of the DOM cycle lie molecular-level relationships between the individual compounds in DOM ...

  1. Carbon allocation in underground storage organs

    OpenAIRE

    Turesson, Helle

    2014-01-01

    By increasing knowledge of carbon allocation in underground storage organs and using the knowledge to improve such crops, the competitiveness of these types of storage organs can be strengthened. Starch is the most common storage compound in tubers and roots, but some crops accumulate compounds other than starch. This thesis examined representative underground storage organs accumulating starch, oil and sugars. These were: the oil-accumulating nutsedge (Cyperus esculentus), a half-grass whic...

  2. Calcium Carbonate

    Science.gov (United States)

    ... before being swallowed; do not swallow them whole. Drink a full glass of water after taking either the regular or chewable tablets or capsules. Some liquid forms of calcium carbonate must be shaken well before use.Do not ...

  3. Carbon Stars

    Indian Academy of Sciences (India)

    T. Lloyd Evans

    2010-12-01

    In this paper, the present state of knowledge of the carbon stars is discussed. Particular attention is given to issues of classification, evolution, variability, populations in our own and other galaxies, and circumstellar material.

  4. Synthesis, Characterization and Biological Activities of Organotin (IV Methylcyclohexyldithiocarbamate Compounds

    Directory of Open Access Journals (Sweden)

    Normah Awang

    2011-01-01

    Full Text Available Problem statement: The growing interest in the chemistry of sulphur donor ligands are due to their encouraging anticancer, antibacterial and antifungal activities as well as their widespread industrial application. Dithiocarbamates belong to this class and much attention has been paid to them. Approach: Novel organotin compounds with the molecular formula RmSn[S2CN(CH3(C6H11]4-m (where m = 2, R = CH3, C2H5; m = 3, R = C6H5 have been synthesized using in situ method. These compounds were characterized by elemental analysis, IR, 1H and 13C NMR spectroscopy. Results: Elemental analysis revealed that all compounds were of good purity. Infrared spectra of the compounds showed that the thioureide ν(C-N band was in the region 1450-1500 cm−1. The unsplitting band of ν(C-S in the region 974-979 cm−1 indicated the bidentate nature of the chelated dithiocarbamato legends. The 13C NMR chemical shift of the carbon atom in the N-CS2 group appeared in the range of 196.29-199.82 ppm. Single crystal analysis from one of these compounds showed that the chelating mode of the dithiocarbamate groups was isobidentate. These compounds have been screened for antibacterial activity against four bacteria; Staphylococcus aureus, Salmonella typhimurium, Pseudomonas aeruginosa and Bacillus subtilis. Only one of these compounds shows promising results against S. aureus and S. typhi. Cytotoxicity screening on human leukemic promyelocyte HL-60 cells found that two of these compounds were very active with CD50 values of 0.87 and 0.18 µg mL−1. Conclusion: The studied compounds were found to have the potential in biological activity especially in cytotoxicity where this possibly can be used for clinical trials after further research.

  5. VOLATILE ORGANIC COMPOUNDS REMOVAL METHODS: A REVIEW

    Directory of Open Access Journals (Sweden)

    Aydin Berenjian

    2012-01-01

    Full Text Available Volatile Organic Compounds (VOCs are among the most toxic chemicals which are detrimental to humans and environment. There is a significant need of fully satisfactory method for removal of VOCs. There are several methods including physical, chemical and biological treatments available to remove VOCs by either recovery or destruction. The aim of the present study is to summarize the available methods for VOC removal; trying to find a promising method among the available techniques. A wide range of VOCs can be treated biologically in which it offers advantages over more traditional processes including lower operating and capital costs and a smaller carbon footprint. However, due to a complex nature and diversity of VOCs it is hard to find a simple and promising method. Treatment still requires more research to solve the associate problems with available VOC elimination techniques.

  6. II-VI semiconductor compounds

    CERN Document Server

    1993-01-01

    For condensed matter physicists and electronic engineers, this volume deals with aspects of II-VI semiconductor compounds. Areas covered include devices and applications of II-VI compounds; Co-based II-IV semi-magnetic semiconductors; and electronic structure of strained II-VI superlattices.

  7. Cytotoxic Compounds from Zanthoxylum Americanum

    Institute of Scientific and Technical Information of China (English)

    2000-01-01

    Four pyranocoumarins: dipetaline, alloxanthoxyletin, xanthoxyletin, and xanthyletin, and two lignans: sesamin and asarinin were isolated from the northern prickly ash, Zanthoxylum americanum. To varying degrees, all six compounds inhibited the incorporation of tritiated thymidine into human leukemia (HL-60) cells and the inhibitory effect was dependent on the structures of the isolated compounds.

  8. Proton and helium stopping cross sections in gaseous hydrocarbon compounds

    International Nuclear Information System (INIS)

    Proton and 4He ion stopping powers were measured for various hydrocarbon gases in the energy ranges 60-750 keV and 100-1050 keV, respectively. The statistical and systematical errors are about 1% each. The target compounds, which contain different types of carbon-carbon bonds, were n-alkanes Csub(n)Hsub(2n+2)(n=1-10), 1-alkenes Csub(n)Hsub(2n)(n=2-4), 1-alkynes Csub(n)Hsub(2n-2)(n=5-7), acetylene C2H2 and (1,3)-butadiene C4H6. Thus, this experiment provides a large data base for a Bragg-rule analysis with hydrocarbon compounds. (orig.)

  9. Bis(adamantan-1-aminium carbonate

    Directory of Open Access Journals (Sweden)

    Monika Nowakowska

    2012-04-01

    Full Text Available In the title compound, 2C10H18N+·CO32−, the adamantan-1-aminium cation forms three N—H...O hydrogen bonds to three carbonate ions, resulting in a layer parallel to (001 with the adamantane groups located on its surface so that adjacent layers form only C—H...H—C contacts. The carbonate anions occupy special positions of 32 symmetry, whereas the adamantan-1-aminium cations occupy special positions of 3 symmetry.

  10. Carbon-bearing iron phases and the carbon isotope composition of the deep Earth

    OpenAIRE

    Horita, Juske; Polyakov, Veniamin B.

    2014-01-01

    Due to its bonding environments, carbon can make up numerous compounds with many other elements. However, the abundance and dynamics of carbon in the deep Earth remains uncertain due to its complex behavior during the primary accretion and differentiation of the Earth in its early history. The naturally occurring stable isotopes of carbon serve as a useful tracer to study the carbon cycle, both on the surface and in the deep Earth. Here, a new model is presented for understanding a first-orde...

  11. Bilayer Effects of Antimalarial Compounds.

    Directory of Open Access Journals (Sweden)

    Nicole B Ramsey

    Full Text Available Because of the perpetual development of resistance to current therapies for malaria, the Medicines for Malaria Venture developed the Malaria Box to facilitate the drug development process. We tested the 80 most potent compounds from the box for bilayer-mediated effects on membrane protein conformational changes (a measure of likely toxicity in a gramicidin-based stopped flow fluorescence assay. Among the Malaria Box compounds tested, four compounds altered membrane properties (p< 0.05; MMV007384 stood out as a potent bilayer-perturbing compound that is toxic in many cell-based assays, suggesting that testing for membrane perturbation could help identify toxic compounds. In any case, MMV007384 should be approached with caution, if at all.

  12. Optimizing Synthetic Aperture Compound Imaging

    DEFF Research Database (Denmark)

    Hansen, Jens Munk; Jensen, Jørgen Arendt

    2012-01-01

    Spatial compound images are constructed from synthetic aperture data acquired using a linear phased-array transducer. Compound images of wires, tissue, and cysts are created using a method, which allows both transmit and receive compounding without any loss in temporal resolution. Similarly to...... optimal for lesion detection. Synthetic aperture data are acquired from unfocused emissions and 154 compound images are constructed by synthesizing different aperture configurations with more or less compounding, all maintaining a constant resolution across depth corresponding to an f-number of 2.0 for...... transmit and receive. The same configurations are used for scanning a phantom with cysts, and it is demonstrated how an improved cysts contrast follows from an aperture configuration, which gives a higher value for the performance measure extracted from the phantom without cysts. A correlation value R = 0...

  13. Gas-liquid transfer of aroma compounds during winemaking fermentations

    OpenAIRE

    Mouret, Jean-Roch; Morakul, Sumallika; Nicolle, Pamela; Athes, Violaine; Sablayrolles, Jean-Marie

    2012-01-01

    We precisely monitored the production kinetics of 16 volatile carbon compounds corresponding to the predominant higher alcohols and esters produced during the alcoholic fermentation of wine using an online GC system. We studied the gas-liquid partitioning of isobutanol, isoamyl acetate and ethyl hexanoate and showed that CO2 stripping had no impact on the partition coefficient (k(i)). We formulated a predictive model for k(i) changes during the fermentation and calculated the gas-liquid balan...

  14. ELECTRICAL AND MAGNETIC PROPERTIES OF GADOLINIUM AND TERBIUM CLUSTER COMPOUNDS

    OpenAIRE

    Bauhofer, W.; Cockcroft, J; Kremer, R.; Mattausch, Hj.; Schwarz, C.; Simon, A.

    1988-01-01

    Gadolinium and terbium halides with halogen-to-metal ratios X/M < 2 contain distorted octahedral M6 units with a differing degree of condensation. With M2X3 being the only exception, additional non-metal atoms (hydrogen, carbon, silicon, nitrogen) occupy the cavities of the M6 units. The electrical behavior ranges from insulating to metallic. Temperature dependent metal-to-semiconductor transitions are observed for several compounds. The majority of the investigated materials exhibits antifer...

  15. Thermal degradation of the vapours of organic nitrogen compounds in the presence of the air

    International Nuclear Information System (INIS)

    Following a quick survey of the literature on the products originated during the thermal degradation of some organic nitrogen compounds, the experimental results obtained by applying a technique previously used for other organic compounds are presented. The compounds investigated include: methyl and ethylamines at the origin of the bad smells of many gaseous wastes, trilaurylamine and tetraethylenediamine sometimes used in nuclear facilities. Attention is brought on the emission of noxious products during thermal degradation in the presence of the air, at various temperatures, viz. either usual combustion gases such as carbon monoxide, or nitro-derivatives such as hydrogen cyanide present whatever the compound investigated when temperatures are below 8500C

  16. Genetic, molecular, and morphological analysis of compound leaf development.

    Science.gov (United States)

    Goliber, T; Kessler, S; Chen, J J; Bharathan, G; Sinha, N

    1999-01-01

    Leaves, the plant organs responsible for capturing and converting most of the 170 billion metric tons of carbon fixed globally each year, can be broadly grouped into two morphological categories: simple and compound. Although simple-leaved species such as corn and Arabidopsis have traditionally been favored model systems for studying leaf development, recent years have seen an increase in genetic and molecular studies of compound leaf development. Two compound-leaved species in particular have emerged as model systems: tomato and pea. A variety of mutations which alter leaf morphology in these species have been described, and analyses of these mutations have allowed the construction of testable models of leaf development. Also, the knotted-like homeobox (KNOX) genes, which were originally discovered as regulators of meristem function, now appear to have a role in compound leaf development. In addition to the recent genetic and molecular analyses of tomato and pea, insight into the nature of compound leaf development may be gained through the study of (a) heteroblasty and heterophylly, phenomena in which a range of leaf forms can be produced by a single shoot, and (b) the evolutionary origins of compound leaves. PMID:9891889

  17. Mechanisms of carbon aging and their effects on the retention of organic iodides by carbon

    International Nuclear Information System (INIS)

    The activated carbon used to treat the off-gas from the Savannah River Plant production reactor building was studied to determine the chemical changes occuring in this carbon during its service life. The carbon is a coconut-shell charcoal impregnated with 1% triethylenediamine (TEDA) and 2% KI. It was known that during its 30-month service life the carbon becomes more acidic and less effective for retaining iodine in organic form. The study showed that the most important change occurring in the carbon is the reaction of KI to give other chemical forms of iodine. The results suggest that the carbon reacts with KI to form organic compounds, but small amounts of oxidized iodine may also be present. The TEDA impregnant is lost from the carbon very quickly, and has no importance after a few months. Mathematical analysis of the carbon performance data show that they are consistent with the reaction of iodide impregnant with impurities in the air flowing through the carbon bed. Additional mathematical analysis, based on electron microscopic observation of the carbon particles, indicates that the external surfaces of the carbon are mainly responsible for their effectiveness in retaining iodine. Consequently, the condition of the impregnants on a relatively small fraction of the carbon surface can have a large effect on its performance. (author)

  18. The impact of lateral carbon fluxes on the European carbon balance

    Science.gov (United States)

    Ciais, P.; Borges, A. V.; Abril, G.; Meybeck, M.; Folberth, G.; Hauglustaine, D.; Janssens, I. A.

    2008-09-01

    To date, little is known about the impact of processes which cause lateral carbon fluxes over continents, and from continents to oceans on the CO2 and carbon budgets at local, regional and continental scales. Lateral carbon fluxes contribute to regional carbon budgets as follows: Ecosystem CO2 sink=Ecosystem carbon accumulation+Lateral carbon fluxes. We estimated the contribution of wood and food product trade, of emission and oxidation of reduced carbon species, and of river erosion and transport as lateral carbon fluxes to the carbon balance of Europe (EU-25). The analysis is completed by new estimates of the carbon fluxes of coastal seas. We estimated that lateral transport (all processes combined) is a flux of 165 Tg C yr-1 at the scale of EU-25. The magnitude of lateral transport is thus comparable to current estimates of carbon accumulation in European forests. The main process contributing to the total lateral flux out of Europe is the flux of reduced carbon compounds, corresponding to the sum of non-CO2 gaseous species (CH4, CO, hydrocarbons, ...) emitted by ecosystems and exported out of the European boundary layer by the large scale atmospheric circulation.

  19. The impact of lateral carbon fluxes on the European carbon balance

    Directory of Open Access Journals (Sweden)

    P. Ciais

    2008-09-01

    Full Text Available To date, little is known about the impact of processes which cause lateral carbon fluxes over continents, and from continents to oceans on the CO2 – and carbon budgets at local, regional and continental scales. Lateral carbon fluxes contribute to regional carbon budgets as follows: Ecosystem CO2 sink=Ecosystem carbon accumulation+Lateral carbon fluxes. We estimated the contribution of wood and food product trade, of emission and oxidation of reduced carbon species, and of river erosion and transport as lateral carbon fluxes to the carbon balance of Europe (EU-25. The analysis is completed by new estimates of the carbon fluxes of coastal seas. We estimated that lateral transport (all processes combined is a flux of 165 Tg C yr−1 at the scale of EU-25. The magnitude of lateral transport is thus comparable to current estimates of carbon accumulation in European forests. The main process contributing to the total lateral flux out of Europe is the flux of reduced carbon compounds, corresponding to the sum of non-CO2 gaseous species (CH4, CO, hydrocarbons, ... emitted by ecosystems and exported out of the European boundary layer by the large scale atmospheric circulation.

  20. The Atmospheric Fate of Organic Nitrogen Compounds

    Science.gov (United States)

    Borduas, Nadine

    Organic nitrogen compounds are present in our atmosphere from biogenic and anthropogenic sources and have impacts on air quality and climate. Due to recent advances in instrumentation, these compounds are being detected in the gas and particle phases, raising questions as to their source, processing and sinks in the environment. With their recently identified role as contributors to aerosol formation and growth, their novel large scale use as solvents in carbon capture and storage (CCS) technology and their emissions from cigarette smoke, it is now important to address the gaps in our understanding of the fate of organic nitrogen. Experimentally and theoretically, I studied the chemical atmospheric fate of specific organic nitrogen compounds in the amine, amide and isocyanate families, yielding information that can be used in chemical transport models to assess the fate of this emerging class of atmospheric molecules. I performed kinetic laboratory studies in a smog chamber to measure the room temperature rate coefficient for reaction with the hydroxyl radical of monoethanolamine, nicotine, and five different amides. I employed online-mass spectrometry techniques to quantify the oxidation products. I found that amines react quickly with OH radicals with lifetimes of a few hours under sunlit conditions, producing amides as oxidation products. My studies on amides revealed that they have much longer lifetimes in the atmosphere, ranging from a few hours to a week. Photo-oxidation of amides produces isocyanates and I investigated these mechanisms in detail using ab initio calculations. Furthermore, I experimentally measured isocyanic acid's Henry's Law constant as well as its hydrolysis rate constants to better understand its sinks in the atmosphere. Finally, I re-examined the structure-activity relationship (SAR) of organic nitrogen molecules for improved model parameterizations.

  1. FIELD SCREENING FOR HALOGENATED VOLATILE ORGANIC COMPOUNDS

    Energy Technology Data Exchange (ETDEWEB)

    John F. Schabron; Joseph F. Rovani Jr.; Theresa M. Bomstad

    2002-06-01

    Western Research Institute (WRI) initiated exploratory work towards the development of new field screening methodology and a test kit to measure halogenated volatile organic compounds (VOCs) in the field. Heated diode and corona discharge sensors are commonly used to detect leaks of refrigerants from air conditioners, freezers, and refrigerators. They are both selective to the presence of carbon-halogen bonds. Commercially available heated diode and corona discharge leak detectors were procured and evaluated for halogenated VOC response. The units were modified to provide a digital readout of signal related to VOC concentration. Sensor response was evaluated with carbon tetrachloride and tetrachloroethylene (perchloroethylene, PCE), which represent halogenated VOCs with and without double bonds. The response characteristics were determined for the VOCs directly in headspace in Tedlar bag containers. Quantitation limits in air were estimated. Potential interferences from volatile hydrocarbons, such as toluene and heptane, were evaluated. The effect of humidity was studied also. The performance of the new devices was evaluated in the laboratory by spiking soil samples and monitoring headspace for halogenated VOCs. A draft concept of the steps for a new analytical method was outlined. The results of the first year effort show that both devices show potential utility for future analytical method development work towards the goal of developing a portable test kit for screening halogenated VOCs in the field.

  2. Volatile halogenated compounds and chlorophenols in the Skagerrak

    Science.gov (United States)

    Abrahamsson, Katarina; Ekdahl, Anja

    1996-02-01

    A total of 680 seawater samples were collected and analysed for volatile halogenated organic compounds, and 280 seawater samples were analysed for chlorinated phenols in the Skagerrak. The sampling was done along three transects along the Danish west coast on five occasions during the years 1991 to 1993. Pentachlorophenol (PCP) was the only chlorophenol detected on all occasions, which implies that it is transported as a dissolved species rather than particle bound. The results indicate that the origin of PCP in the Skagerrak is the Baltic and the coastal areas of Sweden and Norway. The biogenic volatile halocarbons constitute the largest fraction of the halocarbons in the area. The data support the findings that volatile chloroethenes are naturally produced. Therefore, the Skagerrak acts as a source for these compounds. The flux of the compounds investigated is directed from the sea to the atmosphere except for carbon tetrachloride.

  3. Hexaphosphapentaprismane: a new gateway to organophosphorus cage compound chemistry.

    Science.gov (United States)

    al-Ktaifani, Mahmoud M; Bauer, Walter; Bergsträsser, Uwe; Breit, Bernhard; Francis, Matthew D; Heinemann, Frank W; Hitchcock, Peter B; Mack, Andreas; Nixon, John F; Pritzkow, Hans; Regitz, Manfred; Zeller, Matthias; Zenneck, Ulrich

    2002-06-01

    Several independent synthetic routes are described leading to the formation of a novel unsaturated tetracyclic phosphorus carbon cage compound tBu4C4P6 (1), which undergoes a light-induced valence isomerization to produce the first hexaphosphapentaprismane cage tBu4C4P6 (2). A second unsaturated isomer tBu4C4P6 (9) of 1 and the bis-[W(CO)5] complex 13 of 1 are stable towards similar isomerization reactions. Another starting material for the synthesis of the hexaphosphapentaprismane cage tBu4C4P6 (2) is the trimeric mercury complex [(tBu4C4P6)Hg]3 (11), which undergoes elimination of mercury to afford the title compound 2. Single-crystal X-ray structural determinations have been carried out on compounds 1, 2, 9, 11, and 13. PMID:12180342

  4. Volatile and semivolatile organic compounds in laboratory peat fire emissions

    Science.gov (United States)

    George, Ingrid J.; Black, Robert R.; Geron, Chris D.; Aurell, Johanna; Hays, Michael D.; Preston, William T.; Gullett, Brian K.

    2016-05-01

    In this study, volatile and semi-volatile organic compound (VOCs and SVOCs) mass emission factors were determined from laboratory peat fire experiments. The peat samples originated from two National Wildlife Refuges on the coastal plain of North Carolina, U.S.A. Gas- and particle-phase organic compounds were quantified by gas chromatography-mass spectrometry and by high pressure liquid chromatography. Hazardous air pollutants (HAPs) accounted for a large fraction (∼60%) of the speciated VOC emissions from peat burning, including large contributions of acetaldehyde, formaldehyde, benzene, toluene, and chloromethane. In the fine particle mass (PM2.5), the following organic compound classes were dominant: organic acids, levoglucosan, n-alkanes, and n-alkenes. Emission factors for the organic acids in PM2.5 including n-alkanoic acids, n-alkenoic acids, n-alkanedioic acids, and aromatic acids were reported for the first time for peat burning, representing the largest fraction of organic carbon (OC) mass (11-12%) of all speciated compound classes measured in this work. Levoglucosan contributed to 2-3% of the OC mass, while methoxyphenols represented 0.2-0.3% of the OC mass on a carbon mass basis. Retene was the most abundant particulate phase polycyclic aromatic hydrocarbon (PAH). Total HAP VOC and particulate PAH emissions from a 2008 peat wildfire in North Carolina were estimated, suggesting that peat fires can contribute a large fraction of state-wide HAP emissions.

  5. Regulation of Compound Leaf Development

    Directory of Open Access Journals (Sweden)

    Yuan Wang

    2013-12-01

    Full Text Available Leaf morphology is one of the most variable, yet inheritable, traits in the plant kingdom. How plants develop a variety of forms and shapes is a major biological question. Here, we discuss some recent progress in understanding the development of compound or dissected leaves in model species, such as tomato (Solanum lycopersicum, Cardamine hirsuta and Medicago truncatula, with an emphasis on recent discoveries in legumes. We also discuss progress in gene regulations and hormonal actions in compound leaf development. These studies facilitate our understanding of the underlying regulatory mechanisms and put forward a prospective in compound leaf studies.

  6. Enhanced Growth and Redox Characteristics of Some Conducting Polymers on Carbon Nanotube Modified Electrodes

    Institute of Scientific and Technical Information of China (English)

    R.Saraswathi

    2007-01-01

    1 Results Recent studies on the electrochemistry of a number of active compounds at carbon nanotube electrodes have proved beyond doubt their excellent electrocatalytic properties.Particularly,the advancements accomplished towards the functionalization of carbon nanotubes resulting in their enhanced solubilization in aqueous solutions have helped in the preparation of stable carbon nanotube electrodes.Glassy carbon has been invariably the preferred substrate for casting carbon nanotube electrodes.Such c...

  7. Current views on the regulation of autotrophic carbon dioxide fixation via the Calvin cycle in bacteria

    OpenAIRE

    Dijkhuizen, L; Harder, W

    1984-01-01

    The Calvin cycle of carbon dioxide fixation constitutes a biosynthetic pathway for the generation of (multi-carbon) intermediates of central metabolism from the one-carbon compound carbon dioxide. The product of this cycle can be used as a precursor for the synthesis of all components of cell material. Autotrophic carbon dioxide fixation is energetically expensive and it is therefore not surprising that in the various groups of autotrophic bacteria the operation of the cycle is under strict m...

  8. Depletion of compounds from thin oil films in seawater

    International Nuclear Information System (INIS)

    When oil is spilled on water, the oil compounds distribute between droplets and water-soluble phases in the water column. Some small organic acids, phenols, BTEX, and aromatic compounds will dissolve completely, but larger polycyclic aromatic hydrocarbons (PAH) and alkanes will remain in the droplet fraction. The biodegradation of droplets occurs at the oil-water interface. A method for immobilizing the oil films onto hydrophobic surfaces was developed in order to obtain a stable oil surface during the biodegradation period. A test system was also established to determine the depletion of oil compounds from the oil phase, including both abiotic and biotic processes. Three North Sea oils were used in the study. Two were paraffinic oils rich in n-alkanes and aromatic compounds, and one was asphalthenic which was richer in branched alkanes and PAH. The biodegradation period was 2 months at 13 degrees C. Samples from the water and thin film on the fabric was analyzed for carbon 10 and carbon 36 by gas chromatography-flame ionization detection. Semi-volatile organic compounds were analyzed using gas chromatography-mass spectrometry. Results indicated that the depletion process for alkanes was completely caused by biodegradation, while aromatic compounds were depleted by abiotic dissolution as well as by biodegradation. The system has potential for determining oil depletion processes under controlled surface-to-volume conditions, such as thin oil films and dispersed oil droplets. In addition, the system can be used to determine the depletion process in flow-through systems. 13 refs., 3 tabs., 9 figs

  9. Carbon particles

    Science.gov (United States)

    Hunt, Arlon J.

    1984-01-01

    A method and apparatus whereby small carbon particles are made by pyrolysis of a mixture of acetylene carried in argon. The mixture is injected through a nozzle into a heated tube. A small amount of air is added to the mixture. In order to prevent carbon build-up at the nozzle, the nozzle tip is externally cooled. The tube is also elongated sufficiently to assure efficient pyrolysis at the desired flow rates. A key feature of the method is that the acetylene and argon, for example, are premixed in a dilute ratio, and such mixture is injected while cool to minimize the agglomeration of the particles, which produces carbon particles with desired optical properties for use as a solar radiant heat absorber.

  10. Non-carbon nanotubes: synthesis and simulation

    International Nuclear Information System (INIS)

    The discovery of a new allotropic form of carbon, extended nanometre-sized quasi-unidimensional tubular structures (carbon nanotubes), as well as broad prospects for the use of nanomaterials based on them initiated numerous studies in the search for, and design of, nanotubular structures based in other compounds. Some properties and the main methods for the synthesis of non-carbon nanotubes are considered. Studies on the simulation of the electronic structures of these unique objects are analysed. Results of experimental and theoretical studies along these lines are discussed. The bibliography includes 328 references.

  11. Non-carbon nanotubes: synthesis and simulation

    International Nuclear Information System (INIS)

    The discovery of a new allotropic form of carbon, extended nano-sized quasi-unidimensional tubular structures (carbon nanotubes) and the broad prospects for the use of nanomaterials based on them have initiated numerous studies on the search and design of nanotubular structures of other substances. Some properties and the main methods of synthesis of non-carbon nanotubes based in particular, on boron compounds molybdenum, tungsten, niobium chalcogenides and vanadium oxides are considered. The works on the simulation of the electronic structures of these unique objects are analysed. The results of experimental and theoretical studies along these lines are discussed

  12. A Terpene Synthase Is Involved in the Synthesis of the Volatile Organic Compound Sodorifen of Serratia plymuthica 4Rx13

    OpenAIRE

    Domik, Dajana; Thürmer, Andrea; Weise, Teresa; Brandt, Wolfgang; Daniel, Rolf; Piechulla, Birgit

    2016-01-01

    Bacteria release a plethora of volatile organic compounds, including compounds with extraordinary structures. Sodorifen (IUPAC name: 1,2,4,5,6,7,8-heptamethyl-3-methylenebicyclo[3.2.1]oct-6-ene) is a recently identified and unusual volatile hydrocarbon that is emitted by the rhizobacterium Serratia plymuthica 4R×13. Sodorifen comprises a bicyclic ring structure solely consisting of carbon and hydrogen atoms, where every carbon atom of the skeleton is substituted with either a methyl or a meth...

  13. A terpene synthase is involved in the synthesis of the volatile organic compound sodorifen of Serratia plymuthica 4Rx13

    OpenAIRE

    Dajana eDomik; Andrea eThürmer; Teresa eWeise; Wolfgang eBrandt; Rolf eDaniel; Birgit ePiechulla

    2016-01-01

    Bacteria release a plethora of volatile organic compounds (VOCs), including compounds with extraordinary structures. Sodorifen (IUPAC name: 1,2,4,5,6,7,8-heptamethyl-3-methylenebicyclo[3.2.1]oct-6-ene) is a recently identified and unusual volatile hydrocarbon that is emitted by the rhizobacterium Serratia plymuthica 4Rx13. Sodorifen comprises a bicyclic ring structure solely consisting of carbon and hydrogen atoms, where every carbon atom of the skeleton is substituted with either a methyl or...

  14. Carbon classified?

    DEFF Research Database (Denmark)

    Lippert, Ingmar

    2012-01-01

    . Using an actor- network theory (ANT) framework, the aim is to investigate the actors who bring together the elements needed to classify their carbon emission sources and unpack the heterogeneous relations drawn on. Based on an ethnographic study of corporate agents of ecological modernisation over a...... corporations construing themselves as able and suitable to manage their emissions, and, additionally, given that the construction of carbon emissions has performative consequences, the underlying practices need to be declassified, i.e. opened for public scrutiny. Hence the paper concludes by arguing for a...

  15. Explorations of soil microbial processes driven by dissolved organic carbon

    NARCIS (Netherlands)

    Straathof, A.L.

    2015-01-01

    Explorations of soil microbial processes driven by dissolved organic carbon Angela L. Straathof June 17, 2015, Wageningen UR ISBN 978-94-6257-327-7 Abstract Dissolved organic carbon (DOC) is a complex, heterogeneous mixture of C compounds which, as

  16. Crystallographic properties of fertilizer compounds

    Energy Technology Data Exchange (ETDEWEB)

    Frazier, A.W.; Dillard, E.F.; Thrasher, R.D.; Waerstad, K.R.; Hunter, S.R.; Kohler, J.J.; Scheib, R.M.

    1991-02-01

    This bulletin is a compilation of crystallographic data collected at NFERC on 450 fertilizer-related compounds. In TVA's fertilizer R and D program, petrographic examination, XRD, and infrared spectroscopy are combined with conventional chemical analysis methods in identifying the individual compounds that occur in fertilizer materials. This handbook brings together the results of these characterization studies and supplemental crystallographic data from the literature. It is in one-compound-per-page, loose-leaf format, ordered alphabetically by IUPAC name. Indexes provided include IUPAC name, formula, group, alternate formula, synonyms, x-ray data, optical data. Tables are given for solids, compounds in commercial MAP and DAP, and matrix materials in phosphate rock.

  17. The precipitation of vanadium compounds

    International Nuclear Information System (INIS)

    The results of a study on the chemistry of the precipitation process of vanadium compounds in sulfuric media are presented, in order to recover the vanadium contained in the ore from Campo Alegre de Lourdes (Bahia-Brazil). (Author)

  18. Optimization of compound gear pump

    Institute of Scientific and Technical Information of China (English)

    栾振辉

    2002-01-01

    This paper introduces the performances of compound gear pump. Based on the target of having the smallest mass per unit volume, the paper established a mathematical model of optimization, and obtained the results of optimization of the pump.

  19. Fourth symposium on macrocyclic compounds

    International Nuclear Information System (INIS)

    Both theoretical and experimental aspects of the properties and behavior of synthetic and naturally occurring macrocyclic compounds are covered in this symposium. This document contains abstracts of the papers

  20. The demise of compound houses

    DEFF Research Database (Denmark)

    Andreasen, Jørgen; Eskemose Andersen, Jørgen

    2006-01-01

    The compound house has long provided the accomodation required by low income households in West African cities. In Kumasi, Ghana, evidence suggests that no new compounds are being built. Instead, the city is being ringed by relatively affluent villa-style development while neighbourhoods dominated...... the neighbourhood unity is a challenge for urban planners. However they represent good value for money, cost little to build, suit traditional inheritence patterns, allow independent life at low cost and allow sharing of services with a finite and known group (albeit within a potential conflictive...... characteristics of compound housing and analyses the advantages and disadvantages of life within such housing in Kumasi. Issues of privacy, image and communal life are usually cited by occupants dissatiesfied with life in compound houses, and the difficulty of extending them without spoiling the open spaces and...

  1. Compounding in synthetic aperture imaging

    DEFF Research Database (Denmark)

    Hansen, J. M.; Jensen, J. A.

    2012-01-01

    A method for obtaining compound images using synthetic aperture data is investigated using a convex array transducer. The new approach allows spatial compounding to be performed for any number of angles without reducing the frame rate or temporal resolution. This important feature is an intrinsic...... from multiple spherical emissions to synthesize multiple transmit and receive apertures, corresponding to imaging the tissue from multiple directions. The many images are added incoherently, to produce a single compound image. Using a 192-element, 3.5-MHz, λ-pitch transducer, it is demonstrated from...... tissue-phantom measurements that the speckle is reduced and the contrast resolution improved when applying synthetic aperture compound imaging. At a depth of 4 cm, the size of the synthesized apertures is optimized for lesion detection based on the speckle information density. This is a performance...

  2. Quality control of labelled compounds

    International Nuclear Information System (INIS)

    Some advantages and disadvantages of methods used for quality control of organic labelled compounds (131I, 14C) are shortly discussed. The methods used are electrophoresis, ultraviolet and infrared spectrometry, radiogas and thin-layer chromatography. (author)

  3. Phenolic Compounds in Brassica Vegetables

    Directory of Open Access Journals (Sweden)

    Pablo Velasco

    2010-12-01

    Full Text Available Phenolic compounds are a large group of phytochemicals widespread in the plant kingdom. Depending on their structure they can be classified into simple phenols, phenolic acids, hydroxycinnamic acid derivatives and flavonoids. Phenolic compounds have received considerable attention for being potentially protective factors against cancer and heart diseases, in part because of their potent antioxidative properties and their ubiquity in a wide range of commonly consumed foods of plant origin. The Brassicaceae family includes a wide range of horticultural crops, some of them with economic significance and extensively used in the diet throughout the world. The phenolic composition of Brassica vegetables has been recently investigated and, nowadays, the profile of different Brassica species is well established. Here, we review the significance of phenolic compounds as a source of beneficial compounds for human health and the influence of environmental conditions and processing mechanisms on the phenolic composition of Brassica vegetables.

  4. Multi-angle compound imaging

    DEFF Research Database (Denmark)

    Jespersen, Søren Kragh; Wilhjelm, Jens Erik; Sillesen, Henrik

    1998-01-01

    This paper reports on a scanning technique, denoted multi-angle compound imaging (MACI), using spatial compounding. The MACI method also contains elements of frequency compounding, as the transmit frequency is lowered for the highest beam angles in order to reduce grating lobes. Compared to...... conventional B-mode imaging MACI offers better defined tissue boundaries and lower variance of the speckle pattern, resulting in an image with reduced random variations. Design and implementation of a compound imaging system is described, images of rubber tubes and porcine aorta are shown and effects on...... visualization are discussed. The speckle reduction is analyzed numerically and the results are found to be in excellent agreement with existing theory. An investigation of detectability of low-contrast lesions shows significant improvements compared to conventional imaging. Finally, possibilities for improving...

  5. Third Symposium on Macrocyclic Compounds

    International Nuclear Information System (INIS)

    At the Third Symposium on Macrocyclic Compounds there were sessions on facilitated transport, analytical applications, organic synthesis and reactions, phase transfer catalysis, and metal complexation. Abstracts of the individual presentations are included

  6. Structural Library of Natural Compounds

    Directory of Open Access Journals (Sweden)

    Subhash Chandra Bose Kotte

    2011-07-01

    Full Text Available Natural products with biological activity are of considerable interest to drug discovery community and a structural library of such compounds serves as data set for insilico experiments to predict the target specific activity before screening them in in-vitro experiments. This work leverages open source scientific tools to create a database of such compounds library in Structure Data Format with 3D coordinates which in turn may be used as an input file for various applications.

  7. Phenolic Compounds in Brassica Vegetables

    OpenAIRE

    Pablo Velasco; María Elena Cartea; Pilar Soengas; Marta Francisco

    2011-01-01

    Phenolic compounds are a large group of phytochemicals widespread in the plant kingdom. Depending on their structure they can be classified into simple phenols, phenolic acids, hydroxycinnamic acid derivatives and flavonoids. Phenolic compounds have received considerable attention for being potentially protective factors against cancer and heart diseases, in part because of their potent antioxidative properties and their ubiquity in a wide range of commonly consumed foods of plant origin. The...

  8. Transplacental Transfer of Perfluorinated Compounds

    OpenAIRE

    Adhikari, M.

    2015-01-01

    Humans are exposed to chemical carcinogens and endocrine disruptors for instances through environment and diet they consume. Special attention should be paid to pregnant mothers in whom consumption of any harmful compounds can lead to adverse effects in a new born baby as it is believed that these compounds pass through the placenta. The developing foetus is vulnerable to toxic and teratogenic effects and the prenatal exposure of chemicals might lead to developmental changes or even increase ...

  9. Sulfated compounds from marine organisms.

    Science.gov (United States)

    Kornprobst, J M; Sallenave, C; Barnathan, G

    1998-01-01

    More than 500 sulfated compounds have been isolated from marine organisms so far but most of them originate from two phyla only, Spongia and Echinodermata. The sulfated compounds are presented according to the phyla they have been identified from and to their chemical structures. Biological activities, when available, are also given. Macromolecules have also been included in this review but without structural details. PMID:9530808

  10. Antitumor compounds from marine actinomycetes.

    OpenAIRE

    Salas, José A.; Carmen Méndez; Carlos Olano

    2009-01-01

    Chemotherapy is one of the main treatments used to combat cancer. A great number of antitumor compounds are natural products or their derivatives, mainly produced by microorganisms. In particular, actinomycetes are the producers of a large number of natural products with different biological activities, including antitumor properties. These antitumor compounds belong to several structural classes such as anthracyclines, enediynes, indolocarbazoles, isoprenoides, macrolides, non-ribosomal pept...

  11. Cancer chemoprevention by natural compounds

    OpenAIRE

    スズキ, マスミ; Masumi, SUZUI

    2007-01-01

    There is growing interest in the use of natural compounds for the treatment and prevention of a wide variety of diseases, including cancer. Several herb-derived components are currently evaluated in preclinical studies as potential cancer chemopreventive agents. We have recently found that several herbal plants in the Ryukyu Islands, or any other natural compound, have a potential chemopreventive effect on biomarkers of colon carcinogenesis and a growth inhibitory effect on human cancer cells...

  12. Insertion compounds of uranium oxides

    International Nuclear Information System (INIS)

    Insertion compounds are formed by the intercalation of an electropositive species, such as hydrogen or an alkali metal, with minimal structural rearrangement of the host oxide. In this report a review of the measured structural, thermodynamic and transport properties of the insertion compounds of α-U3O8, α-UO3, γ-UO3, δ-UO3 and related systems is given. (author)

  13. Antitumor Immunity and Dietary Compounds

    Directory of Open Access Journals (Sweden)

    Annalise R. Smith

    2013-12-01

    Full Text Available The mechanisms by which natural dietary compounds exert their antitumor effects have been the focus of a large number of research efforts in recent years. Induction of apoptosis by inhibition of cell proliferative pathways is one of the common means of cell death employed by these dietary compounds. However, agents that can activate an antitumor immune response in addition to a chemotherapeutic effect may be useful adjuvants or alternative therapies for the treatment of cancer. The focus of this review is to highlight representative dietary compounds, namely Withania somnifera, Panax ginseng, curcumin and resveratrol with special emphasis on their antitumor immune mechanism of action. Each of these dietary compounds and their sources has a history of safe human use as food or in herbal medicine traditions, potentially making them ideal therapeutics. Here we report the recent advances in the cellular immune mechanisms utilized by these compounds to induce antitumor immunity. Taken together, these findings provide a new perspective for exploiting novel dietary compounds as chemoimmunotherapeutic anti-cancer agents.

  14. Electrical conductivity of short carbon fibers and carbon black-reinforced chloroprene rubber

    International Nuclear Information System (INIS)

    Elastomers and plastics are intrinsically insulating materials, but by addition of some conductive particles such as conductive carbon black, carbon fibers and metals, they can change to conductive form. Conductivity of these composites are due to formation of the lattices of conductive filler particles in polymer chains. In this report, conductivity of chloroprene rubber filled with carbon black and carbon fibers as a function of temperature and pressure are studied. Electrical conductivity of chloroprene in a function of temperature and pressure are studied. Electrical conductivity of chloroprene in the presence of carbon black with proper mixing conditions increases to the conductivity level of semiconductors and even in the presence of carbon fibers it increases to the level of a conductor material. Meanwhile, the sensitivity of this compound to heat and pressure rises. Thus these composites have found various applications in the manufacture of heat and pressure sensitive sensors

  15. Carbon Requirement of Hendersonula Toruloidea Nattress

    Directory of Open Access Journals (Sweden)

    G. C. Saxena

    1970-04-01

    Full Text Available Effect of 8 different carbon compounds on the growth of Hendersonula toruloidea Nattrass, that causes brown rot of fruits of Malus sylvestris Mill has been studied. Galactose was the best; maltose, glucose, sucrose also supported good growth. Growth was moderate with glycerol and lactose but poor with starch.

  16. Development of an automatic sampling device for the continuous measurement of atmospheric carbonyls compounds

    International Nuclear Information System (INIS)

    Two sampling strategies were studied to develop an automatic instrument for the continuous measurement of atmospheric carbonyl compounds. Because of its specificity towards carbonyls compounds, sampling by using a transfer of gaseous phase in a liquid phase associated with a simultaneous chemical derivatization of the trapped compounds was first studied. However, this method do not allow a quantitative sampling of all studied carbonyl compounds, nor a continuous measurement in the field. To overcome the difficulties, a second strategy was investigated: the cryogenic adsorption onto solid adsorbent followed by thermodesorption and a direct analysis by GC/MS. Collection efficiency using different solid adsorbents was found greater than 95% for carbonyl compounds consisting of 1 to 7 carbons. This work is a successful first step towards the realization of the automatic sampling device for a continuous measurement of atmospheric carbonyls compounds. (author)

  17. Supercritical carbon dioxide: a solvent like no other

    Directory of Open Access Journals (Sweden)

    Jocelyn Peach

    2014-08-01

    Full Text Available Supercritical carbon dioxide (scCO2 could be one aspect of a significant and necessary movement towards green chemistry, being a potential replacement for volatile organic compounds (VOCs. Unfortunately, carbon dioxide has a notoriously poor solubilising power and is famously difficult to handle. This review examines attempts and breakthroughs in enhancing the physicochemical properties of carbon dioxide, focusing primarily on factors that impact solubility of polar and ionic species and attempts to enhance scCO2 viscosity.

  18. Supercritical carbon dioxide: a solvent like no other

    OpenAIRE

    Jocelyn Peach; Julian Eastoe

    2014-01-01

    Supercritical carbon dioxide (scCO2) could be one aspect of a significant and necessary movement towards green chemistry, being a potential replacement for volatile organic compounds (VOCs). Unfortunately, carbon dioxide has a notoriously poor solubilising power and is famously difficult to handle. This review examines attempts and breakthroughs in enhancing the physicochemical properties of carbon dioxide, focusing primarily on factors that impact solubility of polar and ionic species and at...

  19. Electrochemistry of silicon in chloro-fluoride and carbonate melts

    Directory of Open Access Journals (Sweden)

    Devyatkin S.V.

    2003-01-01

    Full Text Available The electrochemical behavior of K2SiF6 in chloro-fluoride melts and that of SiO2 in carbonate melts has been studied. Silicon, titanium silicides, boron silicide and ternary compounds Ti-Si-B have been deposited from chloro-fluoride melts. Only SiC was deposited from carbonate-silica melts under carbon dioxide atmosphere (that is, excessive pressure of CO2.

  20. Fabrication of Pt deposited on carbon nanotubes and performance of its polymer electrolyte membrane fuel cells

    Institute of Scientific and Technical Information of China (English)

    2002-01-01

    A new method of depositing nano-sized Pt particles on the surface of the carbon nano-tubes was introduced, and the performance of Pt/carbon nanotube compound on polymer electrolyte membrane fuel cells was measured. The experimental results show that the fine platinum particles (about 3 nm) were well dispersed on carbon nanotubes, which demonstrates the excellent catalytic properties of the Pt/CNTs compound in polymer electrolyte membrane fuel cells.