Science.gov

Sample records for acid gases carbon

  1. Carbonate acidizing

    SciTech Connect

    Daccord, G.; Touboul, E.; Lenormand, R.

    1989-02-01

    The authors present the first quantitative study and complete model of the wormholing phenomenon, leading to a means of predicting and optimizing carbonate acidizing treatments. Laboratory experiments on a gypsum model system and computer simulations show that for a given geometry, wormholes can be quantified by a unique parameter, their equivalent hydraulic length. The behavior of this quantifying parameter vs. all the system parameters is studied and allows the quantitative prediction of the efficiency of an acidizing treatment. This study highlights the fractal nature of the phenomenon, which is accounted for in the equations, and the strong effect of the sample geometry. Three types of etching can be obtained: compact, wormhole type, or homogeneous. The optimum conditions for achieving the best skin decrease correspond to the creation of wormholes and can then be defined in terms of fluid reactivity and injection rate.

  2. Adsorption of Gases on Carbon Nanotubes

    NASA Astrophysics Data System (ADS)

    Mbaye, Mamadou Thiao

    This research focus in studying the interaction between various classical and quantum gases with novel carbon nanostructures, mainly carbon nanotubes (CNTs). Since their discovery by the Japanese physicist Sumio Iijima [1] carbon nanotubes have, experimentally and theoretically, been subjected to many scientific investigation. Studies of adsorption on CNTs are particularly directed toward their better usage in gas storage, gas separation, catalyst, drug delivery, and water purification. We explore the adsorption of different gases entrapped in a single, double, or multi-bundles of CNTs using computer simulations. The first system we investigate consists of Ar and Kr films adsorbed on zigzag or armchair nanotubes. Our simulations revealed that Kr atoms on intermediate size zigzag NTs undergo two phase transitions: A liquid-vapor (L?V), and liquid-commensurate (L?CS) with a fractional coverage of one Kr atoms adsorbed for every four carbon atoms. For Ar on zigzag and armchair NTs, the only transition observed is a L?V. In the second problem, we explore the adsorption of CO2 molecules in a nanotube bundle and calculate the isosteric heat of adsorption of the entrapped molecules within the groove. We observed that the lower the temperature, the higher the isosteric of adsorption. Last, we investigate the adsorption of hydrogen, Helium, and Neon gases on the groove site of two parallel nanotubes. At low temperature, the transverse motion on the plane perpendicular to the tubes' axis is frozen out and as a consequence, the heat capacity is reduced to 1/2. At high temperature, the atoms gain more degree of freedom and as a consequence the heat capacity is 5/2.

  3. Clostridium strain which produces acetic acid from waste gases

    DOEpatents

    Gaddy, J.L.

    1997-01-14

    A method and apparatus are disclosed for converting waste gases from industrial processes such as oil refining, carbon black, coke, ammonia, and methanol production, into useful products. The method includes introducing the waste gases into a bioreactor where they are fermented to various organic acids or alcohols by anaerobic bacteria within the bioreactor. These valuable end products are then recovered, separated and purified. In an exemplary recovery process, the bioreactor raffinate is passed through an extraction chamber into which one or more non-inhibitory solvents are simultaneously introduced to extract the product. Then, the product is separated from the solvent by distillation. Gas conversion rates can be maximized by use of centrifuges, hollow fiber membranes, or other means of ultrafiltration to return entrained anaerobic bacteria from the bioreactor raffinate to the bioreactor itself, thus insuring the highest possible cell concentration. 4 figs.

  4. Clostridium stain which produces acetic acid from waste gases

    DOEpatents

    Gaddy, James L.

    1997-01-01

    A method and apparatus for converting waste gases from industrial processes such as oil refining, carbon black, coke, ammonia, and methanol production, into useful products. The method includes introducing the waste gases into a bioreactor where they are fermented to various organic acids or alcohols by anaerobic bacteria within the bioreactor. These valuable end products are then recovered, separated and purified. In an exemplary recovery process, the bioreactor raffinate is passed through an extraction chamber into which one or more non-inhibitory solvents are simultaneously introduced to extract the product. Then, the product is separated from the solvent by distillation. Gas conversion rates can be maximized by use of centrifuges, hollow fiber membranes, or other means of ultrafiltration to return entrained anaerobic bacteria from the bioreactor raffinate to the bioreactor itself, thus insuring the highest possible cell concentration.

  5. Rare gases, water, and carbon in kaersutites

    NASA Astrophysics Data System (ADS)

    Poreda, Robert J.; Basu, Asish R.

    1984-07-01

    Kaersutites from Kakanui, New Zealand and from three localities in the southwestern United States have been analyzed for rare gases, water and carbon to investigate the volatile signature of the sub-continental mantle. This study does not confirm the high 3He/ 4He and 21Ne/ 22Ne ratios reported by Saito et al. [1] for the Kakanui kaersutite. Instead, a 3He/ 4He ratio of 6 RA and atmospheric 21Ne/ 22Ne ratios were measured which are consistent with our current knowledge of the earth's mantle. A low 40Ar/ 36Ar of 320 and more than 10 -8 cm 3/g of 36Ar confirms the argon results of Saito et al. and indicates that significant quantities of 36Ar reside in this portion of the mantle. Kaersutites from the southwestern United States (Arizona) have a heterogeneous helium isotope signature, ranging from 8.8 RA at San Carlos to 0.46 at Hoover Dam. All D/H ratios for the water in kaersutites (-56 to -78) represent typical mantle values with no apparent correlation with 3He/ 4He. The correlation of increasing carbon content (140-400 ppm) with increasing ? 13C (-24.5 to -16.7) may reflect differences in the proportions of oxidized and reduced carbon in these samples.

  6. Processes to remove acid forming gases from exhaust gases

    DOEpatents

    Chang, S.G.

    1994-09-20

    The present invention relates to a process for reducing the concentration of NO in a gas, which process comprises: (A) contacting a gas sample containing NO with a gaseous oxidizing agent to oxidize the NO to NO[sub 2]; (B) contacting the gas sample of step (A) comprising NO[sub 2] with an aqueous reagent of bisulfite/sulfite and a compound selected from urea, sulfamic acid, hydrazinium ion, hydrazoic acid, nitroaniline, sulfanilamide, sulfanilic acid, mercaptopropanoic acid, mercaptosuccinic acid, cysteine or combinations thereof at between about 0 and 100 C at a pH of between about 1 and 7 for between about 0.01 and 60 sec; and (C) optionally contacting the reaction product of step (A) with conventional chemical reagents to reduce the concentrations of the organic products of the reaction in step (B) to environmentally acceptable levels. Urea or sulfamic acid are preferred, especially sulfamic acid, and step (C) is not necessary or performed. 16 figs.

  7. Processes to remove acid forming gases from exhaust gases

    DOEpatents

    Chang, Shih-Ger (El Cerrito, CA)

    1994-01-01

    The present invention relates to a process for reducing the concentration of NO in a gas, which process comprises: (A) contacting a gas sample containing NO with a gaseous oxidizing agent to oxidize the NO to NO.sub.2 ; (B) contacting the gas sample of step (A) comprising NO.sub.2 with an aqueous reagent of bisulfite/sulfite and a compound selected from urea, sulfamic acid, hydrazinium ion, hydrazoic acid, nitroaniline, sulfanilamide, sulfanilic acid, mercaptopropanoic acid, mercaptosuccinic acid, cysteine or combinations thereof at between about 0.degree. and 100.degree. C. at a pH of between about 1 and 7 for between about 0.01 and 60 sec; and (C) optionally contacting the reaction product of step (A) with conventional chemical reagents to reduce the concentrations of the organic products of the reaction in step (B) to environ-mentally acceptable levels. Urea or sulfamic acid are preferred, especially sulfamic acid, and step (C) is not necessary or performed.

  8. How Acidic Is Carbonic Acid?

    PubMed

    Pines, Dina; Ditkovich, Julia; Mukra, Tzach; Miller, Yifat; Kiefer, Philip M; Daschakraborty, Snehasis; Hynes, James T; Pines, Ehud

    2016-03-10

    Carbonic, lactic, and pyruvic acids have been generated in aqueous solution by the transient protonation of their corresponding conjugate bases by a tailor-made photoacid, the 6-hydroxy-1-sulfonate pyrene sodium salt molecule. A particular goal is to establish the pKa of carbonic acid H2CO3. The on-contact proton transfer (PT) reaction rate from the optically excited photoacid to the carboxylic bases was derived, with unprecedented precision, from time-correlated single-photon-counting measurements of the fluorescence lifetime of the photoacid in the presence of the proton acceptors. The time-dependent diffusion-assisted PT rate was analyzed using the Szabo-Collins-Kimball equation with a radiation boundary condition. The on-contact PT rates were found to follow the acidity order of the carboxylic acids: the stronger was the acid, the slower was the PT reaction to its conjugate base. The pKa of carbonic acid was found to be 3.49 ± 0.05 using both the Marcus and Kiefer-Hynes free energy correlations. This establishes H2CO3 as being 0.37 pKa units stronger and about 1 pKa unit weaker, respectively, than the physiologically important lactic and pyruvic acids. The considerable acid strength of intact carbonic acid indicates that it is an important protonation agent under physiological conditions. PMID:26862781

  9. What are functional ionic liquids for the absorption of acidic gases?

    PubMed

    Ren, Shuhang; Hou, Yucui; Tian, Shidong; Chen, Xiumei; Wu, Weize

    2013-02-28

    As a kind of novel and efficient material, ionic liquids (ILs) are used for capture of acidic gases including SO2 and CO2 from flue gas. Due to very low content of acidic gases in flue gas, it is important to find functional ILs to absorb the acidic gases. However, up to now, there is no criterion to distinguish if the ILs are functional or not before use, which greatly influences the design of functional ILs. In this work, a series of ILs were synthesized and used to determine functional or normal ILs for the capture of acidic gases. It has been found that the pKa of organic acids forming the anion of ILs can be used to differentiate functional ILs from normal ILs for the capture of acidic gases from flue gas. If the pKa of an organic acid is larger than that of sulfurous acid (or carbonic acid), the ILs formed by the organic acid can be called functional ILs for SO2 (or CO2) capture, and it can have a high absorption capacity of SO2 (or CO2) with low SO2 (or CO2) concentrations. If not, the IL is just a normal IL. The pKa of organic acids can also be used to explain the absorption mechanism and guide the synthesis of functional ILs. PMID:23360403

  10. Method of producing pyrolysis gases from carbon-containing materials

    DOEpatents

    Mudge, Lyle K.; Brown, Michael D.; Wilcox, Wayne A.; Baker, Eddie G.

    1989-01-01

    A gasification process of improved efficiency is disclosed. A dual bed reactor system is used in which carbon-containing feedstock materials are first treated in a gasification reactor to form pyrolysis gases. The pyrolysis gases are then directed into a catalytic reactor for the destruction of residual tars/oils in the gases. Temperatures are maintained within the catalytic reactor at a level sufficient to crack the tars/oils in the gases, while avoiding thermal breakdown of the catalysts. In order to minimize problems associated with the deposition of carbon-containing materials on the catalysts during cracking, a gaseous oxidizing agent preferably consisting of air, oxygen, steam, and/or mixtures thereof is introduced into the catalytic reactor at a high flow rate in a direction perpendicular to the longitudinal axis of the reactor. This oxidizes any carbon deposits on the catalysts, which would normally cause catalyst deactivation.

  11. Method of removing carbon monoxide from gases

    DOEpatents

    Gerstein, Bernard C.; Macaulay, David B.

    1976-06-01

    A process and catalyst are disclosed for purifying an atmosphere containing carbon monoxide by passing the atmosphere through a bed of a catalyst of TbO.sub.x, where x = 1.8 to 1.5, which oxidizes the carbon monoxide to carbon dioxide.

  12. Method for removing acid gases from a gaseous stream

    DOEpatents

    Gorin, Everett (San Rafael, CA); Zielke, Clyde W. (McMurray, PA)

    1981-01-01

    In a process for hydrocracking a heavy aromatic polynuclear carbonaceous feedstock containing reactive alkaline constituents to produce liquid hydrocarbon fuels boiling below about 475.degree. C. at atmospheric pressure by contacting the feedstock with hydrogen in the presence of a molten metal halide catalyst, thereafter separating a gaseous stream containing hydrogen, at least a portion of the hydrocarbon fuels and acid gases from the molten metal halide and regenerating the molten metal halide, thereby producing a purified molten metal halide stream for recycle to the hydrocracking zone, an improvement comprising; contacting the gaseous acid gas, hydrogen and hydrocarbon fuels-containing stream with the feedstock containing reactive alkaline constituents to remove acid gases from the acid gas containing stream. Optionally at least a portion of the hydrocarbon fuels are separated from gaseous stream containing hydrogen, hydrocarbon fuels and acid gases prior to contacting the gaseous stream with the feedstock.

  13. Immersing carbon nanotubes in cold atomic gases

    NASA Astrophysics Data System (ADS)

    Wei, C. T.; Mironova, P. V.; Fortgh, J.; Schleich, W. P.; Walser, R.

    2013-10-01

    We investigate the sympathetic relaxation of a free-standing, vibrating carbon nanotube that is mounted on an atom chip and is immersed in a cloud of ultracold atoms. Gas atoms colliding with the nanotube excite phonons via a Casimir-Polder potential. We use Fermi's golden rule to estimate the relaxation rates for relevant experimental parameters and develop a fully dynamic theory of relaxation for the multimode phononic field embedded in a thermal atomic reservoir. Based on currently available experimental data, we identify the relaxation rates as a function of atom density and temperature that are required for sympathetic ground-state cooling of carbon nanotubes.

  14. THE SOLUBILITY OF ACID GASES IN METHANOL

    EPA Science Inventory

    The report describes a thermodynamic model developed to predict phase-equilibrium behavior in a methanol/carbon-dioxide/nitrogen/hydrogen-sulfide system based on parameters determined from binary vapor/liquid equilibrium data available in the literature. Model predictions are com...

  15. MULTIPOLLUTANT MERCURY AND ACID GASES CONTROL TECHNOLOGY

    EPA Science Inventory

    Plans are to continue testing for acid gas, mercury and NOx removal on baseline CFB operation with lime slurry, then use modified lime hydrates and slurries, and modified calcium silicates as additives for enhanced mercury and SO2 removal. Also, data from a coal-fired utility b...

  16. Adsorption of gases on carbon molecular sieves

    SciTech Connect

    Vyas, S.N.; Patwardhan, S.R.; Vijayalakshmi, S. . Dept. of Chemical Engineering); Ganesh, K.S. )

    1994-12-01

    Adsorption on carbon molecular sieves (CMS) prepared by coke deposition has become an interesting area of adsorption due to its microporous nature and favorable separation factor on size and shape selectivity basis for many gaseous systems. In the present work CMS was synthesized from coconut shell through three major steps, namely, carbonization, activation, and coke deposition by hydrocarbon cracking. The crushed, washed, and sieved granules of coconut shell (particle size 2--3 mm) were pretreated with sodium silicate solution and oven-dried at 150 C to create the inorganic sites necessary for coke deposition. Carbonization and activation of the dried granules were carried out at 800 C, for 30 min each. The activated char thus produced was subjected to hydrocarbon cracking at 600 C for periods varying from 30 to 180 min. The product samples were characterized in terms of adsorption isotherm, kinetic adsorption curve, surface area, pore volume, pore size distribution, and characteristic energy for adsorption by using O[sub 2], N[sub 2], C[sub 2]H[sub 2], CO[sub 2], C[sub 3]H[sub 6], and CH[sub 4].

  17. Carbon isotopic composition of deep carbon gases in an ombrogenous peatland, northwestern Ontario, Canada

    SciTech Connect

    Aravena, R. . Center for Groundwater Research and Wetlands Research Center); Warner, B.G. . Wetlands Research Center and Dept. of Geography); Charman, D.J. . Dept. of Geographical Sciences); Belyea, L.R. . School of Biological Sciences); Mathur, S.P. ); Dinel, H. )

    1993-01-01

    Radiocarbon dating and carbon isotope analyses of deep peat and gases in a small ombrogenous peatland in northwestern Ontario reveals the presence of old gases at depth that are 1000-2000 yr younger than the enclosing peat. The authors suggest that the most likely explanation to account for this age discrepancy is the downward movement by advection of younger dissolved organic carbon for use by fermentation and methanogens bacteria. This study identifies a potentially large supply of old carbon gases in peatlands that should be considered in global carbon models of the terrestrial biosphere.

  18. ACID GASES IN CO2-RICH SUBSURFACE GEOLOGIC ENVIRONMENTS

    SciTech Connect

    Chialvo, Ariel A; Vlcek, Lukas; Cole, David

    2013-01-01

    The analysis of species behavior involving dilute fluid environments has been crucial for the advance of modern solvation thermodynamics through molecular-based formalisms to guide the development of macroscopic regression tools in the description of fluid behavior and correlation of experimental data (Chialvo 2013). Dilute fluid environments involving geologic formations are of great theoretical and practical relevance regardless of the thermodynamic state conditions. The most challenging systems are those involving highly compressible and reactive confined environments, i.e., where small perturbations of pressure and/or temperature can trigger considerable density changes. This in turn can alter significantly the species solvation, their preferential solvation, and consequently, their reactivity with one another and with the surrounding mineral surfaces whose outcome is the modification of the substrate porosity and permeability, and ultimately, the integrity of the mineral substrates. Considering that changes in porosity and permeability resulting from dissolution and precipitation phenomena in confined environments are at the core of the aqueous CO2-mineral interactions, and that caprock integrity (e.g., sealing capacity) depends on these key parameters, it is imperative to gain fundamental understanding of the mineral-fluid interfacial phenomena and fluid-fluid equilibria under mineral confinement at subsurface conditions. In order to undertand the potential effects of acid gases as contaminants of supercritical CO2 streams, in the next section we will discuss the thermodynamic behavior of CO2 fluid systems by addressing two crucial issues in the context of carbon capture, utilization and sequestration (CCUS) technologies: (i) Why should we consider (acid gas) CO2 impurities? and (ii) Why are CO2 fluid - mineral interactions of paramount relevance?

  19. Process for removal of ammonia and acid gases from contaminated waters

    DOEpatents

    King, C.J.; Mackenzie, P.D.

    1982-09-03

    Contaminating basic gases, i.e., ammonia and acid gases, e.g., carbon dioxide, are removed from process waters or waste waters in a combined extraction and stripping process. Ammonia in the form of ammonium ion is extracted by an immiscible organic phase comprising a liquid cation exchange component, especially an organic phosphoric acid derivative, and preferably di-2-ethyl hexyl phosphoric acid, dissolved in an alkyl hydrocarbon, aryl hydrocarbon, higher alcohol, oxygenated hydrocarbon, halogenated hydrocarbon, and mixtures thereof. Concurrently, the acidic gaseous contaminants are stripped from the process or waste waters by stripping with stream, air, nitrogen, or the like. The liquid cation exchange component has the ammonia stripped therefrom by heating, and the component may be recycled to extract additional amounts of ammonia.

  20. Process for removal of ammonia and acid gases from contaminated waters

    DOEpatents

    King, C. Judson; MacKenzie, Patricia D.

    1985-01-01

    Contaminating basic gases, i.e., ammonia, and acid gases, e.g., carbon dioxide, are removed from process waters or waste waters in a combined extraction and stripping process. Ammonia in the form of ammonium ion is extracted by an immiscible organic phase comprising a liquid cation exchange component, especially an organic phosphoric acid derivative, and preferably di-2-ethyl hexyl phosphoric acid, dissolved in an alkyl hydrocarbon, aryl hydrocarbon, higher alcohol, oxygenated hydrocarbon, halogenated hydrocarbon, and mixtures thereof. Concurrently, the acidic gaseous contaminants are stripped from the process or waste waters by stripping with steam, air, nitrogen, or the like. The liquid cation exchange component has the ammonia stripped therefrom by heating, and the component may be recycled to extract additional amounts of ammonia.

  1. 21 CFR 201.161 - Carbon dioxide and certain other gases.

    Code of Federal Regulations, 2014 CFR

    2014-04-01

    ... 21 Food and Drugs 4 2014-04-01 2014-04-01 false Carbon dioxide and certain other gases. 201.161... (CONTINUED) DRUGS: GENERAL LABELING Other Exemptions § 201.161 Carbon dioxide and certain other gases. (a) Carbon dioxide, cyclopropane, ethylene, helium, and nitrous oxide gases intended for drug use...

  2. 21 CFR 201.161 - Carbon dioxide and certain other gases.

    Code of Federal Regulations, 2012 CFR

    2012-04-01

    ... 21 Food and Drugs 4 2012-04-01 2012-04-01 false Carbon dioxide and certain other gases. 201.161... (CONTINUED) DRUGS: GENERAL LABELING Other Exemptions § 201.161 Carbon dioxide and certain other gases. (a) Carbon dioxide, cyclopropane, ethylene, helium, and nitrous oxide gases intended for drug use...

  3. 21 CFR 201.161 - Carbon dioxide and certain other gases.

    Code of Federal Regulations, 2013 CFR

    2013-04-01

    ... 21 Food and Drugs 4 2013-04-01 2013-04-01 false Carbon dioxide and certain other gases. 201.161... (CONTINUED) DRUGS: GENERAL LABELING Other Exemptions § 201.161 Carbon dioxide and certain other gases. (a) Carbon dioxide, cyclopropane, ethylene, helium, and nitrous oxide gases intended for drug use...

  4. Fullerenes: an extraterrestrial carbon carrier phase for noble gases.

    PubMed

    Becker, L; Poreda, R J; Bunch, T E

    2000-03-28

    In this work, we report on the discovery of naturally occurring fullerenes (C60 to C400) in the Allende and Murchison meteorites and some sediment samples from the 65 million-year-old Cretaceous/Tertiary boundary layer (KTB). Unlike the other pure forms of carbon (diamond and graphite), fullerenes are extractable in an organic solvent (e.g., toluene or 1,2,4-trichlorobenzene). The recognition of this unique property led to the detection and isolation of the higher fullerenes in the Kratschmer/Huffmann arc evaporated graphite soot and in the carbon material in the meteorite and impact deposits. By further exploiting the unique ability of the fullerene cage structure to encapsulate and retain noble gases, we have determined that both the Allende and Murchison fullerenes and the KTB fullerenes contain trapped noble gases with ratios that can only be described as extraterrestrial in origin. PMID:10725367

  5. Fullerenes: An extraterrestrial carbon carrier phase for noble gases

    PubMed Central

    Becker, Luann; Poreda, Robert J.; Bunch, Ted E.

    2000-01-01

    In this work, we report on the discovery of naturally occurring fullerenes (C60 to C400) in the Allende and Murchison meteorites and some sediment samples from the 65 million-year-old Cretaceous/Tertiary boundary layer (KTB). Unlike the other pure forms of carbon (diamond and graphite), fullerenes are extractable in an organic solvent (e.g., toluene or 1,2,4-trichlorobenzene). The recognition of this unique property led to the detection and isolation of the higher fullerenes in the Kratschmer/Huffmann arc evaporated graphite soot and in the carbon material in the meteorite and impact deposits. By further exploiting the unique ability of the fullerene cage structure to encapsulate and retain noble gases, we have determined that both the Allende and Murchison fullerenes and the KTB fullerenes contain trapped noble gases with ratios that can only be described as extraterrestrial in origin. PMID:10725367

  6. Process for removal of carbonyl sulfide in liquified hydrocarbon gases with absorption of acid gases

    SciTech Connect

    Beavon, D.K.; Mackles, M.

    1980-11-11

    Liquified hydrocarbon gases containing at least carbonyl sulfide as an impurity are purified by intimately mixing the liquified hydrocarbon gas with an aqueous absorbent for hydrogen sulfide in a hydrolysis zone maintained at a temperature and a pressure sufficient to maintain the liquified hydrocarbon gas in the liquid state and hydrolyze the carbonyl sulfide to hydrogen sulfide and carbon dioxide. The liquified hydrocarbon gas containing at least a portion of the formed carbonyl sulfide and carbon dioxide is separated from the liquid absorbent and passed to an absorption zone where it is contacted with a liquid hydrogen sulfide absorbent where at least the formed hydrogen sulfide is separated from the liquified petroleum gas. A stage of absorption of at least hydrogen sulfide may proceed mixing of the liquified hydrocarbon gas with the absorbent in the hydrolysis reaction zone. The absorbent employed does not combine irreversibly with carbonyl sulfide, hydrogen sulfide, and carbon dioxide, and preferably is an aqueous solution of diethanolamine.

  7. Insights into deep carbon derived from noble gases

    NASA Astrophysics Data System (ADS)

    Lollar, B. Sherwood; Ballentine, C. J.

    2009-08-01

    Science and society are faced with two challenges that are inextricably linked: fossil-fuel energy dependence and rising levels of atmospheric carbon dioxide. Management of remaining hydrocarbon resources, the search for cleaner fuels and increasing interest in subsurface carbon storage all require a better understanding of the deep terrestrial carbon cycle. The coupling of noble gas and carbon chemistry provides an innovative approach to understanding this deep carbon. Whereas carbon geochemistry and isotopic signatures record the history of inorganic and organic reactions that control carbon mobility, the inert noble gases provide unique tracers of fluid origin, transport and age. Together, they have been used to show that groundwater has a key role as both the sink for geologically sequestered carbon dioxide, and in the transport and emplacement of hydrocarbon gas deposits. Furthermore, these tracers have also been used to show that groundwater and subsurface microbiology jointly influence the formation and alteration of fossil-fuel deposits to an extent not previously recognized. The age and distribution of groundwater in fractures in the Earth's crust exert important controls on the Earth's deepest microbial communities.

  8. Arterial Blood Carbonic Acid Inversely Determines Lactic and Organic Acids

    PubMed Central

    Aiken, Christopher Geoffrey Alexander

    2013-01-01

    Objective: To establish that arterial blood carbonic acid varies inversely with lactic acid in accordance with bicarbonate exchanging for lactate across cell membranes through the anion exchange mechanism to maintain the Gibbs-Donnan equilibrium. Study Design: Over 5 years, lactate was measured on all blood gases taken from neonatal admissions, as well as organic acid whenever electrolytes were required. Results: Arterial blood gases from 63 infants given high calcium TPN were analyzed. Twenty two needed continuous positive airways pressure (CPAP) only and 31 intermittent positive pressure ventilation (IPPV) and surfactant followed by CPAP to treat respiratory distress syndrome in 51 and meconium aspiration syndrome in 2. All survived and were free of infection. Excluded gases were those with high and falling lactate soon after delivery representing perinatal asphyxia, and those on dexamethasone. Strong inverse relations between carbonic and lactic acids were found at all gestational ages and, independent of glomerular filtration, between carbonic and organic acids. Lactate (mmol/L) = 62.53 X PCO2 -0.96(mmHg) r2 0.315, n 1232, p <0.001. Sixty divided by PCO2 is a convenient measure of physiological lactate at any given PCO2. In the first week, 9.13 2.57% of arterial gases from infants on IPPV had lactates above 120/PCO2, significantly more than 4.74 2.73% on CPAP (p<0.05) and 2.47 2.39% on no support. Conclusion: Changes in arterial blood carbonic acid cause immediate inverse changes in lactic acid, because their anions interchange across cell membranes according to the Gibbs Donnan equilibrium. Increasing PCO2 from 40 to 120 mmHg decreased lactate from 1.5 mmol/L to 0.5 mmol/L, so that the sum of carbonic and lactic acids increased from 2.72 mmol/L to only 4.17 mmol/L. This helps explain the neuroprotective effect of hypercapnoea and highlights the importance of avoiding any degree of hypocapnoea in infants on IPPV. PMID:24392387

  9. Process for the removal of acid forming gases from exhaust gases and production of phosphoric acid

    DOEpatents

    Chang, Shih-Ger; Liu, David K.

    1992-01-01

    Exhaust gases are treated to remove NO or NO.sub.x and SO.sub.2 by contacting the gases with an aqueous emulsion or suspension of yellow phosphorous preferably in a wet scrubber. The addition of yellow phosphorous in the system induces the production of O.sub.3 which subsequently oxidizes NO to NO.sub.2. The resulting NO.sub.2 dissolves readily and can be reduced to form ammonium ions by dissolved SO.sub.2 under appropriate conditions. In a 20 acfm system, yellow phosphorous is oxidized to yield P.sub.2 O.sub.5 which picks up water to form H.sub.3 PO.sub.4 mists and can be collected as a valuable product. The pressure is not critical, and ambient pressures are used. Hot water temperatures are best, but economics suggest about 50.degree. C. The amount of yellow phosphorus used will vary with the composition of the exhaust gas, less than 3% for small concentrations of NO, and 10% or higher for concentrations above say 1000 ppm. Similarly, the pH will vary with the composition being treated, and it is adjusted with a suitable alkali. For mixtures of NO.sub.x and SO.sub.2, alkalis that are used for flue gas desulfurization are preferred. With this process, better than 90% of SO.sub.2 and NO in simulated flue gas can be removed. Stoichiometric ratios (P/NO) ranging between 0.6 and 1.5 were obtained.

  10. 21 CFR 201.161 - Carbon dioxide and certain other gases.

    Code of Federal Regulations, 2010 CFR

    2010-04-01

    ... 21 Food and Drugs 4 2010-04-01 2010-04-01 false Carbon dioxide and certain other gases. 201.161 Section 201.161 Food and Drugs FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES (CONTINUED) DRUGS: GENERAL LABELING Other Exemptions § 201.161 Carbon dioxide and certain other gases. (a) Carbon dioxide, cyclopropane,...

  11. 21 CFR 201.161 - Carbon dioxide and certain other gases.

    Code of Federal Regulations, 2011 CFR

    2011-04-01

    ... 21 Food and Drugs 4 2011-04-01 2011-04-01 false Carbon dioxide and certain other gases. 201.161 Section 201.161 Food and Drugs FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES (CONTINUED) DRUGS: GENERAL LABELING Other Exemptions § 201.161 Carbon dioxide and certain other gases. (a) Carbon dioxide, cyclopropane,...

  12. Solubility calculations for acid gases in amine blends

    SciTech Connect

    Chakravarty, T.

    1985-01-01

    Treating with alkanolamines is often used to sweeten gases containing only a few parts per million of CO/sub 2/ and H/sub 2/S. Primary amines such as monoethanolamine (MEA) have great affinity for acid gases and are able to produce high purity sweet gas; on the other hand, tertiary amines like methyldiethanolamine (MDEA) have large capacity and are easy to regenerate but, because they do not bind chemically with CO/sub 2/, they are unable to produce a sweetened gas low in this component. Recently, the use of amine blends has become a subject of potentially great commercial importance. Since, the range of possible amines and blend formulations is large, a method for predicting equilibrium solubility is needed. A rigorous thermodynamic model has been developed which uses the extended Debye-Huckel expression, is very similar to one developed for single-amine solutions, and involves the fitting of binary interaction parameters to experimental data. In this work the interaction parameters found to be important in the activity coefficient expression were fitted to each single-acid-gas single-amine subsystem using all published solubility data. The resulting model was then validated by comparing mixed-acid-gas single-amine solubility predictions with published VLE data. MEA-MDEA and DEA-MDEA blends have been studied in detail in this work. It is found that each amine contributes to the overall acid gas solubility in a nonlinear way and that the solubility curves can exhibit maxima and minima as a function of the relative concentrations of the amines.

  13. Biological production of acetic acid from waste gases with Clostridium ljungdahlii

    DOEpatents

    Gaddy, J.L.

    1998-09-15

    A method and apparatus are disclosed for converting waste gases from industrial processes such as oil refining, carbon black, coke, ammonia, and methanol production, into useful products. The method includes introducing the waste gases into a bioreactor where they are fermented to various organic acids or alcohols by anaerobic bacteria within the bioreactor. These valuable end products are then recovered, separated and purified. In an exemplary recovery process, the bioreactor raffinate is passed through an extraction chamber into which one or more non-inhibitory solvents are simultaneously introduced to extract the product. Then, the product is separated from the solvent by distillation. Gas conversion rates can be maximized by use of centrifuges, hollow fiber membranes, or other means of ultrafiltration to return entrained anaerobic bacteria from the bioreactor raffinate to the bioreactor itself, thus insuring the highest possible cell concentration. 5 figs.

  14. Biological production of acetic acid from waste gases with Clostridium ljungdahlii

    DOEpatents

    Gaddy, James L. (Fayetteville, AR)

    1998-01-01

    A method and apparatus for converting waste gases from industrial processes such as oil refining, carbon black, coke, ammonia, and methanol production, into useful products. The method includes introducing the waste gases into a bioreactor where they are fermented to various organic acids or alcohols by anaerobic bacteria within the bioreactor. These valuable end products are then recovered, separated and purified. In an exemplary recovery process, the bioreactor raffinate is passed through an extraction chamber into which one or more non-inhibitory solvents are simultaneously introduced to extract the product. Then, the product is separated from the solvent by distillation. Gas conversion rates can be maximized by use of centrifuges, hollow fiber membranes, or other means of ultrafiltration to return entrained anaerobic bacteria from the bioreactor raffinate to the bioreactor itself, thus insuring the highest possible cell concentration.

  15. Indoor exposures to fine aerosols and acid gases.

    PubMed Central

    Koutrakis, P; Brauer, M; Briggs, S L; Leaderer, B P

    1991-01-01

    Indoor exposures to aerosols and gases are associated with both indoor and outdoor air pollution sources. The identification of sources and the assessment of their relative contribution can be a complicated process due to a) the presence of numerous indoor sources, which can vary from building to building; b) the uncertainties associated with the estimation of the impact of outdoor sources on indoor air quality; c) the interactions between pollutants; and d) the importance of reactions between pollutants and indoor surfaces. It is well established that fine particles (diameter less than or equal to 2.5 microns) originating from outdoor sources such as automobiles, oil and coal combustion, incineration, and diverse industrial activities can penetrate into the indoor environment. Indoor/outdoor ratios, usually varying between 0.4 and 0.8, depend on parameters such as particle size and density, air exchange rate, and the surface-to-volume ratio of the indoor environment. Determining fine particle elemental composition makes it possible to identify the contribution of different outdoor sources. This paper focuses on the origin and the concentration of indoor aerosols and acid gases by highlighting the results from two indoor air quality studies. PMID:1821374

  16. Carbonic Acid Retreatment of Biomass

    SciTech Connect

    Baylor university

    2003-06-01

    This project sought to address six objectives, outlined below. The objectives were met through the completion of ten tasks. (1) Solidify the theoretical understanding of the binary CO{sub 2}/H{sub 2}O system at reaction temperatures and pressures. The thermodynamics of pH prediction have been improved to include a more rigorous treatment of non-ideal gas phases. However it was found that experimental attempts to confirm theoretical pH predictions were still off by a factor of about 1.8 pH units. Arrhenius experiments were carried out and the activation energy for carbonic acid appears to be substantially similar to sulfuric acid. Titration experiments have not yet confirmed or quantified the buffering or acid suppression effects of carbonic acid on biomass. (2) Modify the carbonic acid pretreatment severity function to include the effect of endogenous acid formation and carbonate buffering, if necessary. It was found that the existing severity functions serve adequately to account for endogenous acid production and carbonate effects. (3) Quantify the production of soluble carbohydrates at different reaction conditions and severity. Results show that carbonic acid has little effect on increasing soluble carbohydrate concentrations for pretreated aspen wood, compared to pretreatment with water alone. This appears to be connected to the release of endogenous acids by the substrate. A less acidic substrate such as corn stover would derive benefit from the use of carbonic acid. (4) Quantify the production of microbial inhibitors at selected reaction conditions and severity. It was found that the release of inhibitors was correlated to reaction severity and that carbonic acid did not appear to increase or decrease inhibition compared to pretreatment with water alone. (5) Assess the reactivity to enzymatic hydrolysis of material pretreated at selected reaction conditions and severity. Enzymatic hydrolysis rates increased with severity, but no advantage was detected for the use of carbonic acid compared to water alone. (6) Determine optimal conditions for carbonic acid pretreatment of aspen wood. Optimal severities appeared to be in the mid range tested. ASPEN-Plus modeling and economic analysis of the process indicate that the process could be cost competitive with sulfuric acid if the concentration of solids in the pretreatment is maintained very high ({approx}50%). Lower solids concentrations result in larger reactors that become expensive to construct for high pressure applications.

  17. Carbonic Acid Pretreatment of Biomass

    SciTech Connect

    G. Peter van Walsum; Kemantha Jayawardhana; Damon Yourchisin; Robert McWilliams; Vanessa Castleberry

    2003-05-31

    This project sought to address six objectives, outlined below. The objectives were met through the completion of ten tasks. 1) Solidify the theoretical understanding of the binary CO2/H2O system at reaction temperatures and pressures. The thermodynamics of pH prediction have been improved to include a more rigorous treatment of non-ideal gas phases. However it was found that experimental attempts to confirm theoretical pH predictions were still off by a factor of about 1.8 pH units. Arrhenius experiments were carried out and the activation energy for carbonic acid appears to be substantially similar to sulfuric acid. Titration experiments have not yet confirmed or quantified the buffering or acid suppression effects of carbonic acid on biomass. 2) Modify the carbonic acid pretreatment severity function to include the effect of endogenous acid formation and carbonate buffering, if necessary. It was found that the existing severity functions serve adequately to account for endogenous acid production and carbonate effects. 3) Quantify the production of soluble carbohydrates at different reaction conditions and severity. Results show that carbonic acid has little effect on increasing soluble carbohydrate concentrations for pretreated aspen wood, compared to pretreatment with water alone. This appears to be connected to the release of endogenous acids by the substrate. A less acidic substrate such as corn stover would derive benefit from the use of carbonic acid. 4) Quantify the production of microbial inhibitors at selected reaction conditions and severity. It was found that the release of inhibitors was correlated to reaction severity and that carbonic acid did not appear to increase or decrease inhibition compared to pretreatment with water alone. 5) Assess the reactivity to enzymatic hydrolysis of material pretreated at selected reaction conditions and severity. Enzymatic hydrolysis rates increased with severity, but no advantage was detected for the use of carbonic acid compared to water alone. 6) Determine optimal conditions for carbonic acid pretreatment of aspen wood. Optimal severities appeared to be in the mid range tested. ASPEN-Plus modeling and economic analysis of the process indicate that the process could be cost competitive with sulfuric acid if the concentration of solids in the pretreatment is maintained very high (~50%). Lower solids concentrations result in larger reactors that become expensive to construct for high pressure applications.

  18. Uptake of Ambient Organic Gases to Acidic Sulfate Aerosols

    NASA Astrophysics Data System (ADS)

    Liggio, J.; Li, S.

    2009-05-01

    The formation of secondary organic aerosols (SOA) in the atmosphere has been an area of significant interest due to its climatic relevance, its effects on air quality and human health. Due largely to the underestimation of SOA by regional and global models, there has been an increasing number of studies focusing on alternate pathways leading to SOA. In this regard, recent work has shown that heterogeneous and liquid phase reactions, often leading to oligomeric material, may be a route to SOA via products of biogenic and anthropogenic origin. Although oligomer formation in chamber studies has been frequently observed, the applicability of these experiments to ambient conditions, and thus the overall importance of oligomerization reactions remain unclear. In the present study, ambient air is drawn into a Teflon smog chamber and exposed to acidic sulfate aerosols which have been formed in situ via the reaction of SO3 with water vapor. The aerosol composition is measured with a High Resolution Aerodyne Aerosol Mass Spectrometer (HR-ToF-AMS), and particle size distributions are monitored with a scanning mobility particle sizer (SMPS). The use of ambient air and relatively low inorganic particle loading potentially provides clearer insight into the importance of heterogeneous reactions. Results of experiments, with a range of sulfate loadings show that there are several competing processes occurring on different timescales. A significant uptake of ambient organic gases to the particles is observed immediately followed by a slow shift towards higher m/z over a period of several hours indicating that higher molecular weight products (possibly oligomers) are being formed through a reactive process. The results suggest that heterogeneous reactions can occur with ambient organic gases, even in the presence of ammonia, which may have significant implications to the ambient atmosphere where particles may be neutralized after their formation.

  19. Discrepancy between Measured Serum Total Carbon Dioxide Content and Bicarbonate Concentration Calculated from Arterial Blood Gases

    PubMed Central

    Kim, Youngho; Massie, Larry; Murata, Glen H

    2015-01-01

    Large differences between the concentrations of serum total carbon dioxide (TCO2) and blood gas bicarbonate (HCO3-) were observed in two consecutive simultaneously drawn sets of samples of serum and arterial blood gases in a patient who presented with severe carbon dioxide retention and profound acidemia.These differences could not be explained by the effect of the high partial pressure of carbon dioxide on TCO2, by variations in the dissociation constant of the carbonic acid/bicarbonate system or by faults caused by the algorithms of the blood gas apparatus that calculate HCO3-. A recalculation using the Henderson-Hasselbach equation revealed arterial blood gas HCO3- values close to the corresponding serum TCO2 values and clarified the diagnosis of the acid-base disorder, which had been placed in doubt by the large differences between the reported TCO2 and HCO3- values.Human error in the calculation of HCO3- was identified as the source of these differences. Recalculation of blood gas HCO3- should be the first step in identifying the source of large differences between serum TCO2 and blood gas HCO3-. PMID:26824002

  20. Joseph Black, carbon dioxide, latent heat, and the beginnings of the discovery of the respiratory gases.

    PubMed

    West, John B

    2014-06-15

    The discovery of carbon dioxide by Joseph Black (1728-1799) marked a new era of research on the respiratory gases. His initial interest was in alkalis such as limewater that were thought to be useful in the treatment of renal stone. When he studied magnesium carbonate, he found that when this was heated or exposed to acid, a gas was evolved that he called "fixed air" because it had been combined with a solid material. He showed that the new gas extinguished a flame, that it could not support life, and that it was present in gas exhaled from the lung. Within a few years of his discovery, hydrogen, nitrogen, and oxygen were also isolated. Thus arguably Black's work started the avalanche of research on the respiratory gases carried out by Priestley, Scheele, Lavoisier, and Cavendish. Black then turned his attention to heat and he was the first person to describe latent heat, that is the heat added or lost when a liquid changes its state, for example when water changes to ice or steam. Latent heat is a key concept in thermal physiology because of the heat lost when sweat evaporates. Black was a friend of the young James Watt (1736-1819) who was responsible for the development of early steam engines. Watt was puzzled why so much cooling was necessary to condense steam into water, and Black realized that the answer was the latent heat. The resulting improvements in steam engines ushered in the Industrial Revolution. PMID:24682452

  1. 75 FR 75059 - Mandatory Reporting of Greenhouse Gases: Injection and Geologic Sequestration of Carbon Dioxide

    Federal Register 2010, 2011, 2012, 2013, 2014

    2010-12-01

    ... Protection Agency 40 CFR Parts 72, 78, and 98 Mandatory Reporting of Greenhouse Gases: Injection and Geologic... 2060-AP88 Mandatory Reporting of Greenhouse Gases: Injection and Geologic Sequestration of Carbon... regulation to require greenhouse gas monitoring and reporting from facilities that conduct...

  2. OPERATION OF A SULFURIC ACID PLANT USING BLENDED COPPER SMELTER GASES

    EPA Science Inventory

    A high degree of control of SOx emissions at copper smelters can be obtained by blending reverberatory furnace gases with gases from roasters and converters and using the combined stream as feed to a sulfuric acid plant. The Bor Copper Smelter in Bor, Yugoslavia, experimented wit...

  3. Atmospheric Trace Gases from the Carbon Dioxide Information Analysis Center (CDIAC)

    DOE Data Explorer

    CDIAC products are indexed and searchable through a customized interface powered by ORNL's Mercury search engine. Products include numeric data packages, publications, trend data, atlases, models, etc. and can be searched for by subject area, keywords, authors, product numbers, time periods, collection sites, spatial references, etc. Some of the collections may also be included in the CDIAC publication, Trends Online: A Compendium of Global Change Data. Most data sets, many with numerous data files, are free to download from CDIAC's ftp area. The collections under the CDIAC heading of Atmospheric Trace Gases include: Atmospheric Carbon Dioxide, Atmospheric Methane, Atmospheric Carbon Monoxide, Atmospheric Hydrogen, Isotopes in Greenhouse Gases, Radionuclides, Aerosols, and Other Trace Gases.

  4. Radiolysis gases from nitric acid solutions containing HSA and HAN

    SciTech Connect

    Smith, J.R.

    1994-10-28

    The concentration of hydrogen (H{sub 2}) in the radiolytically produced off-gas from 2.76-4.25M HNO{sub 3}/PU solutions has been found to be greatly reduced in the presence of sulfamic acid (HSA) and hydroxylamine nitrate (HAN). The H{sub 2} concentration ([H{sub 2}]) is reduced from 35 percent to about 4 percent by dilution caused from an increase in the production rates of nitrogen (N{sub 2}), nitrous oxide (N{sub 2}O), and oxygen (O{sub 2}) gases. The generation rate of H{sub 2} was not affected by HSA or HAN giving a measured radiolytic yield, G(H{sub 2}), value of 0.201 molecules/100 eV for 2.765M NO{sub 3}{sup -} solution (a value of 0.213 is predicted from previous data). The G(H{sub 2}) values are dependent on the solution nitrate concentration ([NO{sub 3}{sup -}]). The generation rates of N{sub 2}, N{sub 2}O, and O{sub 2} are not dependent on the [NO{sub 3}{sup -}] in this narrow range, but are dependent on the presence of HSA and the concentration of HAN. The percentage [H{sub 2}] for the 2.5 to 3.0M NO{sub 3}{sup -} range expected in the off- from the FB-Line Pu{sup +3} Hold Tanks is conservatively estimated to be about 3.5 to 4.5 % for Pu + 3 solutions initially containing 0.023M HAN/0.165M HSA. The upper limit [H{sub 2}] may actually be about 4.1 % (4.3 % at 90 % confidence limits) but more {open_quotes}initial{close_quotes} off-gas rate data is needed at about 2.9M [NO{sub 3}{sup -}] in Pu{sup +3} solution for verification. Addition of ascorbic acid had no effect on the off-gas rate of Pu{sup +3} solutions containing HSA and NO{sub 3}{sup -} concentrations higher than those expected in the hold tanks. The maximum {open_quotes}hold time{close_quotes} for 50 grams/liter Pu{sup +3}/0.165M HSA/0.023M HAN/2.5-3.0M HNO{sub 3} solution is 20.3{+-}2.1 days. After this time the HSA initially present will become exhausted and the [H{sub 2}] will increase to 35 %. This hold time may be longer in [NO{sub 3}{sup -}] < 3.0M, but again more study is needed.

  5. Process for the removal of acid forming gases from exhaust gases

    DOEpatents

    Chang, S.G.; Liu, D.K.

    1992-11-17

    Exhaust gases are treated to remove NO or NO[sub x] and SO[sub 2] by contacting the gases with an aqueous emulsion or suspension of yellow phosphorus preferably in a wet scrubber. The pressure is not critical, and ambient pressures are used. Hot water temperatures are best, but economics suggest about 50 C is attractive. The amount of yellow phosphorus used will vary with the composition of the exhaust gas, less than 3% for small concentrations of NO, and 10% or higher for concentrations above say 1000 ppm. Similarly, the pH will vary with the composition being treated, and it is adjusted with a suitable alkali. For mixtures of NO[sub x] and SO[sub 2], alkalis that are used for flue gas desulfurization are preferred. With this process, 100% of the by-products created are usable, and close to 100% of the NO or NO[sub x] and SO[sub 2] can be removed in an economic fashion. 9 figs.

  6. Process for the removal of acid forming gases from exhaust gases

    DOEpatents

    Chang, Shih-Ger; Liu, David K.

    1992-01-01

    Exhaust gases are treated to remove NO or NO.sub.x and SO.sub.2 by contacting the gases with an aqueous emulsion or suspension of yellow phosphorus preferably in a wet scrubber. The pressure is not critical, and ambient pressures are used. Hot water temperatures are best, but economics suggest about 50.degree. C. are attractive. The amount of yellow phosphorus used will vary with the composition of the exhaust gas, less than 3% for small concentrations of NO, and 10% or higher for concentrations above say 1000 ppm. Similarly, the pH will vary with the composition being treated, and it is adjusted with a suitable alkali. For mixtures of NO.sub.x and SO.sub.2, alkalis that are used for flue gas desulfurization are preferred. With this process, 100% of the by-products created are usable, and close to 100% of the NO or NO and SO.sub.2 can be removed in an economic fashion.

  7. Nanostructured carbon materials for adsorption of methane and other gases

    DOEpatents

    Stadie, Nicholas P.; Fultz, Brent T.; Ahn, Channing; Murialdo, Maxwell

    2015-06-30

    Provided are methods for storing gases on porous adsorbents, methods for optimizing the storage of gases on porous adsorbents, methods of making porous adsorbents, and methods of gas storage of optimized compositions, as in systems containing porous adsorbents and gas adsorbed on the surface of the porous adsorbent. The disclosed methods and systems feature a constant or increasing isosteric enthalpy of adsorption as a function of uptake of the gas onto the exposed surface of a porous adsorbent. Adsorbents with a porous geometry and surface dimensions suited to a particular adsorbate are exposed to the gas at elevated pressures in the specific regime where n/V (density) is larger than predicted by the ideal gas law by more than several percent.

  8. Electrochemical formation of hydroxide for enhancing carbon dioxide and acid gas uptake by a solution

    DOEpatents

    Rau, Gregory Hudson (Castro Valley, CA)

    2012-05-15

    A system is described for forming metal hydroxide from a metal carbonate utilizing a water electrolysis cell having an acid-producing anode and a hydroxyl-producing cathode immersed in a water solution of sufficient ionic content to allow an electric current to pass between the hydroxyl-producing cathode and the acid-producing anode. A metal carbonate, in particular water-insoluble calcium carbonate or magnesium carbonate, is placed in close proximity to the acid-producing anode. A direct current electrical voltage is provided across the acid-producing anode and the hydroxyl-producing cathode sufficient to generate acid at the acid-producing anode and hydroxyl ions at the hydroxyl-producing cathode. The acid dissolves at least part of the metal carbonate into metal and carbonate ions allowing the metal ions to travel toward the hydroxyl-producing cathode and to combine with the hydroxyl ions to form the metal hydroxide. The carbonate ions travel toward the acid-producing anode and form carbonic acid and/or water and carbon dioxide. Among other uses, the metal hydroxide formed can be employed to absorb acid gases such as carbon dioxide from a gas mixture. The invention can also generate hydrogen and oxidative gases such as oxygen or chlorine.

  9. Relation of Hydrogen and Methane to Carbon Monoxide in Exhaust Gases from Internal-Combustion Engines

    NASA Technical Reports Server (NTRS)

    Gerrish, Harold C; Tessmann, Arthur M

    1935-01-01

    The relation of hydrogen and methane to carbon monoxide in the exhaust gases from internal-combustion engines operating on standard-grade aviation gasoline, fighting-grade aviation gasoline, hydrogenated safety fuel, laboratory diesel fuel, and auto diesel fuel was determined by analysis of the exhaust gases. Two liquid-cooled single-cylinder spark-ignition, one 9-cylinder radial air-cooled spark-ignition, and two liquid-cooled single-cylinder compression-ignition engines were used.

  10. Intrapore reaction of carbon fibers with oxygen-containing gases

    SciTech Connect

    Elchina, V.I.; Fridman, L.I.; Gurdzhiyants, V.M.; Ivin, V.D.; Levit, R.M.; Samoilova, N.A.; Yavorskii, I.A.

    1983-01-01

    A study has been made of the conditions of the internal reaction of carbon fiber obtained from polyacrylonitrile under various conditions of heat thermal treatment (the final temperature was varied from 880/sup 0/C to 2400/sup 0/C) with gaseous oxidizing agents: atmospheric oxygen, carbon dioxide, and steam.

  11. Natural sources of greenhouse gases: carbon dioxide emissions from volcanoes

    USGS Publications Warehouse

    Gerlach, Terrence

    1990-01-01

    Volcanic degassing of carbon dioxide plays an important role in keeping the atmosphere-ocean portion of the carbon geochemical cycle in balance. The atmosphere-ocean carbon deficit requires replenishment of 6??1012 mol CO2/yr, and places an upper limit on the output of carbon dioxide from volcanoes. The CO2 output of the global mid-oceanic ridge system is ca. 0.7??1012 mol/yr, thus supplying only a fraction of the amount needed to balance the carbon deficit. The carbon dioxide flux from subaerial volcanoes is poorly known, but it appears to be at least as large as the mid-oceanic ridge flux. Much (perhaps most) of the CO2 emitted from volcanoes is degassed noneruptively. This mode of degassing may lead to impacts on the environment and biosphere that are fundamentally different in character from those envisioned in published scenarios, which are based on the assumption that CO2 degassing occurs predominantly by eruptive processes. Although the flux of carbon dioxide from volcanoes is poorly constrained at present, it is clearly two orders of magnitude lower than the anthropogenic output of CO2.

  12. Process for recovery of sulfur from acid gases

    DOEpatents

    Towler, Gavin P.; Lynn, Scott

    1995-01-01

    Elemental sulfur is recovered from the H.sub.2 S present in gases derived from fossil fuels by heating the H.sub.2 S with CO.sub.2 in a high-temperature reactor in the presence of a catalyst selected as one which enhances the thermal dissociation of H.sub.2 S to H.sub.2 and S.sub.2. The equilibrium of the thermal decomposition of H.sub.2 S is shifted by the equilibration of the water-gas-shift reaction so as to favor elemental sulfur formation. The primary products of the overall reaction are S.sub.2, CO, H.sub.2 and H.sub.2 O. Small amounts of COS, SO.sub.2 and CS.sub.2 may also form. Rapid quenching of the reaction mixture results in a substantial increase in the efficiency of the conversion of H.sub.2 S to elemental sulfur. Plant economy is further advanced by treating the product gases to remove byproduct carbonyl sulfide by hydrolysis, which converts the COS back to CO.sub.2 and H.sub.2 S. Unreacted CO.sub.2 and H.sub.2 S are removed from the product gas and recycled to the reactor, leaving a gas consisting chiefly of H.sub.2 and CO, which has value either as a fuel or as a chemical feedstock and recovers the hydrogen value from the H.sub.2 S.

  13. SOLUBILITIES OF ACID GASES AND NITROGEN IN METHANOL

    EPA Science Inventory

    The report describes a thermodynamic model, developed to predict the equilibrium behavior of carbon dioxide, hydrogen sulfide, nitrogen, and methanol mixtures. The model uses the four-suffix Margules equation to describe liquid-phase nonidealities and the Soave modification of th...

  14. Carbon and Conservation: Cropping systems and greenhouse gases

    Technology Transfer Automated Retrieval System (TEKTRAN)

    Quantifying and predicting soil carbon sequestration and greenhouse gas emissions from agricultural systems have been research goals for numerous institutions, especially since the turn of the millennium. Cost, time, and politics are variables that have limited the rapid development of robust quant...

  15. The Geostationary Remote Infrared Pollution Sounder (GRIPS): measurement of the carbon gases from space

    NASA Astrophysics Data System (ADS)

    Schoeberl, M.; Dickerson, R.; Marshall, B. T.; McHugh, M.; Fish, C.; Bloom, H.

    2013-09-01

    Climate change and air quality are the most pressing environmental issues of the 21st century. Despite decades of research, the sources and sinks of key greenhouse gases remain highly uncertain [IPCC1] making quantitative predictions of atmospheric composition and their impacts. The Geostationary Remote Infrared Pollution Sounder (GRIPS) is a multi-purpose instrument designed to reduce uncertainty associated with atmospheric radiative forcing. GRIPS will measure will measure greenhouse gases and aerosols - two of the most important elements in the earth's radiation budget. GRIPS will observe carbon dioxide (CO2), carbon monoxide (CO), methane (CH4), - the carbon gases, nitrous oxide (N2O), water vapor and aerosols with unprecedented precision through the atmosphere. The GRIPS instrument uses gas filter correlation radiometry (GFCR) to detect reflected and thermal IR radiation to detect the gases and the reflected solar radiation in the visible and short-wave infrared bands for aerosols. GRIPS is designed to have sensitivity down to the Earth's surface at ~2-8km nadir resolution. GRIPS can resolve CO2, CO, and CH4 anomalies in the planetary boundary layer and the free troposphere to quantify lofting, diurnal variations and longrange transport. With repeated measurements throughout the day GRIPS can maximize the number of cloud free measurements determining biogenic and anthropogenic sources, sinks, and fluxes. GRIPS is highly complementary to the Orbiting Carbon Observatory, OCO-2, the geostationary Tropospheric Emissions: Monitoring of Pollution (TEMPO) and Advanced Baseline Imager (ABI) and other existing and planned missions.

  16. ARM Carbon Cycle Gases Flasks at SGP Site

    DOE Data Explorer

    Biraud, Sebastien

    2013-03-26

    Data from flasks are sampled at the Atmospheric Radiation Measurement Program ARM, Southern Great Plains Site and analyzed by the National Oceanic and Atmospheric Administration NOAA, Earth System Research Laboratory ESRL. The SGP site is included in the NOAA Cooperative Global Air Sampling Network. The surface samples are collected from a 60 m tower at the ARM SGP Central Facility, usually once per week in the afternoon. The aircraft samples are collected approximately weekly from a chartered aircraft, and the collection flight path is centered over the tower where the surface samples are collected. The samples are collected by the ARM and LBNL Carbon Project.

  17. A Ni-Doped Carbon Nanotube Sensor for Detecting Oil-Dissolved Gases in Transformers.

    PubMed

    Lu, Jia; Zhang, Xiaoxing; Wu, Xiaoqing; Dai, Ziqiang; Zhang, Jinbin

    2015-01-01

    C2H2, C2H4, and C2H6 are important oil-dissolved gases in power transformers. Detection of the composition and content of oil-dissolved gases in transformers is very significant in the diagnosis and assessment of the state of transformer operations. The commonly used oil-gas analysis methods have many disadvantages, so this paper proposes a Ni-doped carbon nanotube (Ni-CNT) gas sensor to effectively detect oil-dissolved gases in a transformer. The gas-sensing properties of the sensor to C2H2, C2H4, and C2H6 were studied using the test device. Based on the density functional theory (DFT) the adsorption behaviors of the three gases on intrinsic carbon nanotubes (CNTs) and Ni-CNTs were calculated. The adsorption energy, charge transfer, and molecular frontier orbital of the adsorption system were also analyzed. Results showed that the sensitivity of the CNT sensor to the three kinds of gases was in the following order: C2H2 > C2H4 > C2H6. Moreover, the doped Ni improved the sensor response, and the sensor response and gas concentration have a good linear relationship. PMID:26066989

  18. A Ni-Doped Carbon Nanotube Sensor for Detecting Oil-Dissolved Gases in Transformers

    PubMed Central

    Lu, Jia; Zhang, Xiaoxing; Wu, Xiaoqing; Dai, Ziqiang; Zhang, Jinbin

    2015-01-01

    C2H2, C2H4, and C2H6 are important oil-dissolved gases in power transformers. Detection of the composition and content of oil-dissolved gases in transformers is very significant in the diagnosis and assessment of the state of transformer operations. The commonly used oil-gas analysis methods have many disadvantages, so this paper proposes a Ni-doped carbon nanotube (Ni-CNT) gas sensor to effectively detect oil-dissolved gases in a transformer. The gas-sensing properties of the sensor to C2H2, C2H4, and C2H6 were studied using the test device. Based on the density functional theory (DFT) the adsorption behaviors of the three gases on intrinsic carbon nanotubes (CNTs) and Ni-CNTs were calculated. The adsorption energy, charge transfer, and molecular frontier orbital of the adsorption system were also analyzed. Results showed that the sensitivity of the CNT sensor to the three kinds of gases was in the following order: C2H2 > C2H4 > C2H6. Moreover, the doped Ni improved the sensor response, and the sensor response and gas concentration have a good linear relationship. PMID:26066989

  19. Sorption of noble gases by solids, with reference to meteorites. II - Chromite and carbon. III - Sulfides, spinels, and other substances; on the origin of planetary gases

    NASA Technical Reports Server (NTRS)

    Yang, J.; Anders, E.

    1982-01-01

    The trapping of noble gases by chromite and carbon, two putative carriers of primordial noble gases in meteorites, was studied by synthesizing 19 samples in a Ne-Ar-Kr-Xe atmosphere at 440-720 K. Noble gas contents are found to approximately obey Henry's Law, but only slight correlations are found with composition, surface area, or adsorption temperature. Geometric mean distribution coefficients for bulk samples and HCl residues in 10 cu cm STP/g atm are: Xe 100, Kr 15, Ar 3.5, and Ne 0.62. Elemental fractionation data support the suggestion of Lewis et al. (1977) that chromite and carbon in C2 and C3 chondrites were formed by the reaction: Fe, Cr + 4CO yields (Fe, Cr)3O4 + 4C + carbides. In contrast to meteoritic minerals, the synthetic specimens show no isotopic fractionation of noble gases. In a subsequent study, attention is given to the cases of sulfides and spinels, on the way to consideration of the origin of planetary gases. Sulfides showed three distinctive trends relative to chromite or magnetite. The elemental fractionation pattern of Ar, Kr and Xe in meteorites, terrestrial rocks and planets resembles the adsorption patterns on the carbons, spinels, sulfides, and other solids studied. The high release temperature of meteoritic noble gases may be explained by transformation of the physisorbed or chemisorbed gas. The ready loss of meteoritic heavy gases on surficial oxidation is consistent with adsorption, as is the high abundance.

  20. 40 CFR 60.54a - Standard for municipal waste combustor acid gases.

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ... 40 Protection of Environment 7 2013-07-01 2013-07-01 false Standard for municipal waste combustor... for Municipal Waste Combustors for Which Construction is Commenced After December 20, 1989 and on or Before September 20, 1994 60.54a Standard for municipal waste combustor acid gases. (a)-(b) (c) On...

  1. 40 CFR 60.54a - Standard for municipal waste combustor acid gases.

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... 40 Protection of Environment 6 2010-07-01 2010-07-01 false Standard for municipal waste combustor... for Municipal Waste Combustors for Which Construction is Commenced After December 20, 1989 and on or Before September 20, 1994 60.54a Standard for municipal waste combustor acid gases. (a)-(b) (c) On...

  2. 40 CFR 60.54a - Standard for municipal waste combustor acid gases.

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ... 40 Protection of Environment 6 2011-07-01 2011-07-01 false Standard for municipal waste combustor... for Municipal Waste Combustors for Which Construction is Commenced After December 20, 1989 and on or Before September 20, 1994 60.54a Standard for municipal waste combustor acid gases. (a)-(b) (c) On...

  3. 40 CFR 60.54a - Standard for municipal waste combustor acid gases.

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ... 40 Protection of Environment 7 2014-07-01 2014-07-01 false Standard for municipal waste combustor... for Municipal Waste Combustors for Which Construction Is Commenced After December 20, 1989 and On or Before September 20, 1994 60.54a Standard for municipal waste combustor acid gases. (a)-(b) (c) On...

  4. 40 CFR 60.54a - Standard for municipal waste combustor acid gases.

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ... 40 Protection of Environment 7 2012-07-01 2012-07-01 false Standard for municipal waste combustor... for Municipal Waste Combustors for Which Construction is Commenced After December 20, 1989 and on or Before September 20, 1994 60.54a Standard for municipal waste combustor acid gases. (a)-(b) (c) On...

  5. Modeling high-temperature diffusion of gases in micro and mesoporous amorphous carbon

    NASA Astrophysics Data System (ADS)

    Ranganathan, Raghavan; Rokkam, Srujan; Desai, Tapan; Keblinski, Pawel; Cross, Peter; Burnes, Richard

    2015-08-01

    In this work, we study diffusion of gases in porous amorphous carbon at high temperatures using equilibrium molecular dynamics simulations. Microporous and mesoporous carbon structures are computationally generated using liquid quench method and reactive force fields. Motivated by the need to understand high temperature diffusivity of light weight gases like H2, O2, H2O, and CO in amorphous carbon, we investigate the diffusion behavior as function of two important parameters: (a) the pore size and (b) the concentration of diffusing gases. The effect of pore size on diffusion is studied by employing multiple realizations of the amorphous carbon structures in microporous and mesoporous regimes, corresponding to densities of 1 g/cm3 and 0.5 g/cm3, respectively. A detailed analysis of the effect of gas concentration on diffusion in the context of these two porosity regimes is presented. For the microporous structure, we observe that predominantly, a high diffusivity results when the structure is highly anisotropic and contains wide channels between the pores. On the other hand, when the structure is highly homogeneous, significant molecule-wall scattering leads to a nearly concentration-independent behavior of diffusion (reminiscent of Knudsen diffusion). The mesoporous regime is similar in behavior to the highly diffusive microporous carbon case in that diffusion at high concentration is governed by gas-gas collisions (reminiscent of Fickian diffusion), which transitions to a Knudsen-like diffusion at lower concentration.

  6. Modeling high-temperature diffusion of gases in micro and mesoporous amorphous carbon.

    PubMed

    Ranganathan, Raghavan; Rokkam, Srujan; Desai, Tapan; Keblinski, Pawel; Cross, Peter; Burnes, Richard

    2015-08-28

    In this work, we study diffusion of gases in porous amorphous carbon at high temperatures using equilibrium molecular dynamics simulations. Microporous and mesoporous carbon structures are computationally generated using liquid quench method and reactive force fields. Motivated by the need to understand high temperature diffusivity of light weight gases like H2, O2, H2O, and CO in amorphous carbon, we investigate the diffusion behavior as function of two important parameters: (a) the pore size and (b) the concentration of diffusing gases. The effect of pore size on diffusion is studied by employing multiple realizations of the amorphous carbon structures in microporous and mesoporous regimes, corresponding to densities of 1 g/cm(3) and 0.5 g/cm(3), respectively. A detailed analysis of the effect of gas concentration on diffusion in the context of these two porosity regimes is presented. For the microporous structure, we observe that predominantly, a high diffusivity results when the structure is highly anisotropic and contains wide channels between the pores. On the other hand, when the structure is highly homogeneous, significant molecule-wall scattering leads to a nearly concentration-independent behavior of diffusion (reminiscent of Knudsen diffusion). The mesoporous regime is similar in behavior to the highly diffusive microporous carbon case in that diffusion at high concentration is governed by gas-gas collisions (reminiscent of Fickian diffusion), which transitions to a Knudsen-like diffusion at lower concentration. PMID:26328861

  7. ARM-LBNL-NOAA Flask Sampler for Carbon Cycle Gases

    DOE Data Explorer

    Torn, Margaret

    2008-01-15

    Data from ccg-flasks are sampled at the ARM SGP site and analyzed by the NOAA Earth System Research Laboratory (ESRL) as part of the NOAA Cooperative Global Air Sampling Network. Surface samples are collected from a 60m tower at the SGP Central Facility, usually once per week on one afternoon. The aircraft samples are collected approximately weekly from a chartered aircraft, and the collection flight path is centered over the tower where the surface samples are collected. Samples are collected by the ARM/LBNL Carbon Project. CO2 flask data contains measurements of CO2 concentration and CO2 stable isotope ratios (13CO2 and C18OO) from flasks collected at the SGP site. The flask samples are collected at 2m, 4m, 25m, and 60m along the 60m tower.

  8. Carbon dioxide sequestration by direct mineral carbonation with carbonic acid

    SciTech Connect

    O'Connor, W.K.; Dahlin, D.C.; Nilsen, D.N.; Walters, R.P.; Turner, P.C.

    2000-07-01

    The Albany Research Center (ARC) of the US Department of Energy (DOE) has been conducting a series of mineral carbonation tests at its Albany, Oregon, facility over the past 2 years as part of a Mineral Carbonation Study Program within the DOE. The ARC tests have focused on ex-situ mineral carbonation in an aqueous system. The process developed at ARC utilizes a slurry of water mixed with a magnesium silicate mineral, olivine [forsterite and member (mg{sub 2}SiO{sub 4})], or serpentine [Mg{sub 3}Si{sub 2}O{sub 5}(OH){sub 4}]. This slurry is reacted with supercritical carbon dioxide (CO{sub 2}) to produce magnesite (MgCO{sub 3}). The CO{sub 2} is dissolved in water to form carbonic acid (H{sub 2}CO{sub 3}), which dissociates to H{sup +} and HCO{sub 3}{sup {minus}}. The H{sup +} reacts with the mineral, liberating Mg{sup 2+} cations which react with the bicarbonate to form the solid carbonate. The process is designed to simulate the natural serpentinization reaction of ultramafic minerals, and for this reason, these results may also be applicable to in-situ geological sequestration regimes. Results of the baseline tests, conducted on ground products of the natural minerals, have been encouraging. Tests conducted at ambient temperature (22 C) and subcritical CO{sub 2} pressures (below 73 atm) resulted in very slow conversion to the carbonate. However, when elevated temperatures and pressures are utilized, coupled with continuous stirring of the slurry and gas dispersion within the water column, significant reaction occurs within much shorter reaction times. Extent of reaction, as measured by the stoichiometric conversion of the silicate mineral (olivine) to the carbonate, is roughly 90% within 24 hours, using distilled water, and a reaction temperature of 185 C and a partial pressure of CO{sub 2} (P{sub CO{sub 2}}) of 115 atm. Recent tests using a bicarbonate solution, under identical reaction conditions, have achieved roughly 83% conversion of heat treated serpentine and 84% conversion of olivine to the carbonate in 6 hours. The results from the current studies suggest that reaction kinetics can be improved by pretreatment of the mineral, catalysis of the reaction, or some combination of the two. Future tests are intended to examine a broader pressure/temperature regime, various pretreatment options, as well as other mineral groups.

  9. Carbon dioxide sequestration by direct mineral carbonation with carbonic acid

    SciTech Connect

    O'Connor, William K.; Dahlin, David C.; Nilsen, David N.; Walters, Richard P.; Turner, Paul C.

    2000-01-01

    The Albany Research Center (ARC) of the U.S. Dept. of Energy (DOE) has been conducting a series of mineral carbonation tests at its Albany, Oregon, facility over the past 2 years as part of a Mineral Carbonation Study Program within the DOE. Other participants in this Program include the Los Alamos National Laboratory, Arizona State University, Science Applications International Corporation, and the DOE National Energy Technology Laboratory. The ARC tests have focused on ex-situ mineral carbonation in an aqueous system. The process developed at ARC utilizes a slurry of water mixed with a magnesium silicate mineral, olivine [forsterite end member (Mg2SiO4)], or serpentine [Mg3Si2O5(OH)4]. This slurry is reacted with supercritical carbon dioxide (CO2) to produce magnesite (MgCO3). The CO2 is dissolved in water to form carbonic acid (H2CO3), which dissociates to H+ and HCO3 -. The H+ reacts with the mineral, liberating Mg2+ cations which react with the bicarbonate to form the solid carbonate. The process is designed to simulate the natural serpentinization reaction of ultramafic minerals, and for this reason, these results may also be applicable to in-situ geological sequestration regimes. Results of the baseline tests, conducted on ground products of the natural minerals, have been encouraging. Tests conducted at ambient temperature (22 C) and subcritical CO2 pressures (below 73 atm) resulted in very slow conversion to the carbonate. However, when elevated temperatures and pressures are utilized, coupled with continuous stirring of the slurry and gas dispersion within the water column, significant reaction occurs within much shorter reaction times. Extent of reaction, as measured by the stoichiometric conversion of the silicate mineral (olivine) to the carbonate, is roughly 90% within 24 hours, using distilled water, and a reaction temperature of 185?C and a partial pressure of CO2 (PCO2) of 115 atm. Recent tests using a bicarbonate solution, under identical reaction conditions, have achieved roughly 83% conversion of heat treated serpentine and 84% conversion of olivine to the carbonate in 6 hours. The results from the current studies suggest that reaction kinetics can be improved by pretreatment of the mineral, catalysis of the reaction, or some combination of the two. Future tests are intended to examine a broader pressure/temperature regime, various pretreatment options, as well as other mineral groups.

  10. Acid sorption regeneration process using carbon dioxide

    DOEpatents

    King, C. Judson (Kensington, CA); Husson, Scott M. (Anderson, SC)

    2001-01-01

    Carboxylic acids are sorbed from aqueous feedstocks onto a solid adsorbent in the presence of carbon dioxide under pressure. The acids are freed from the sorbent phase by a suitable regeneration method, one of which is treating them with an organic alkylamine solution thus forming an alkylamine-carboxylic acid complex which thermally decomposes to the desired carboxylic acid and the alkylamine.

  11. Flame Synthesis of Carbon Nanotubes Using Low Calorific Value Gases

    SciTech Connect

    Jorge Camacho; Mahesh Subramanya; Ahsan R. Choudhuri

    2007-03-31

    Nanostructures formed in diffusion flames of pure fuels [CH{sub 4}, C{sub 3}H{sub 8}, and C{sub 2}H{sub 2}] at different fuel flow rates have been analyzed. Synthesis samples have been also collected from diffusion flames of various fuel blends [H{sub 2}-CH{sub 4}, H{sub 2}-CO, H{sub 2}-C{sub 3}H{sub 8}, H{sub 2}-C{sub 2}H{sub 2}] at different combustion conditions. SEM images of particulate samples collected from H{sub 2}-CH{sub 4} diffusion flames show formation of nanostructures. However, the formation of nanostructures only occurs at a narrow window of fuel compositions (< 10% H{sub 2} concentration in the mixture) and flow conditions (Jet Exit Reynolds number Re{sub j} = 200). At higher H{sub 2} concentration and flow velocity, formation of nanostructures diminishes and H{sub 2}-CH{sub 4} flames produce amorphous carbon and soot particles.

  12. Molecular equilibria and condensation sequences in carbon rich gases

    NASA Technical Reports Server (NTRS)

    Sharp, C. M.; Wasserburg, G. J.

    1993-01-01

    Chemical equilibria in stellar atmospheres have been investigated by many authors. Lattimer, Schramm, and Grossman presented calculations in both O rich and C rich environments and predicted possible presolar condensates. A recent paper by Cherchneff and Barker considered a C rich composition with PAH's included in the calculations. However, the condensation sequences of C bearing species have not been investigated in detail. In a carbon rich gas surrounding an AGB star, it is often assumed that graphite (or diamond) condenses out before TiC and SiC. However, Lattimer et al. found some conditions under which TiC condenses before graphite. We have performed molecular equilibrium calculations to establish the stability fields of C(s), TiC(s), and SiC(s) and other high temperature phases under conditions of different pressures and C/O. The preserved presolar interstellar dust grains so far discovered in meteorites are graphite, diamond, SiC, TiC, and possibly Al2O3.

  13. Accounting for carbon cycle feedbacks in a comparison of the global warming effects of greenhouse gases

    NASA Astrophysics Data System (ADS)

    Gillett, Nathan P.; Damon Matthews, H.

    2010-07-01

    Greenhouse gases other than CO2 make a significant contribution to human-induced climate change, and multi-gas mitigation strategies are cheaper to implement than those which limit CO2 emissions alone. Most practical multi-gas mitigation strategies require metrics to relate the climate warming effects of CO2 and other greenhouse gases. Global warming potential (GWP), defined as the ratio of time-integrated radiative forcing of a particular gas to that of CO2 following a unit mass emission, is the metric used in the Kyoto Protocol, and we define mean global temperature change potential (MGTP) as an equivalent metric of the temperature response. Here we show that carbon-climate feedbacks inflate the GWPs and MGTPs of methane and nitrous oxide by ~ 20% in coupled carbon-climate model simulations of the response to a pulse of 50 × 1990 emissions, due to a warming-induced release of CO2 from the land biosphere and ocean. The magnitude of this effect is expected to be dependent on the model, but it is not captured at all by the analytical models usually used to calculate metrics such as GWP. We argue that the omission of carbon cycle dynamics has led to a low bias of uncertain but potentially substantial magnitude in metrics of the global warming effect of other greenhouse gases, and we suggest that the carbon-climate feedback should be considered when greenhouse gas metrics are calculated and applied.

  14. Control of Effluent Gases from Solid Waste Processing Using Carbon Nanotubes

    NASA Technical Reports Server (NTRS)

    Fisher, John; Cinke, Martin; Wignarajab, Kanapathipillai

    2005-01-01

    One of the major problems associated with solid waste processing technologies is the release of effluent gases and contaminants that are in gaseous formed from the processes. A number of other gases, in particular NO(x), SO2, NH3, Hydrocarbons (e.g. CH4) do present hazards to the crew in space habitats. Reduction of mass, power, volume and resupply can be achieved by using catalyst impregnated carbon nanotubes as compared to other catalytic systems. The development and characterization of an innovative approach for the control and elimination of gaseous toxins using single walled carbon nanotubes (SWNTs) promise superior performance over conventional approaches. This is due to the ability to direct the selective uptake of gaseous species based on their controllable pore size, high adsorptive capacity and the effectiveness of carbon nanotubes as catalyst supports for gaseous conversion. For example, SWNTs have high adsorptive capacity for NO and the adsorbed NO can be decomposed to N2 and O2 . Experimental results showing the decomposition of NO on metal impregnated carbon nanotubes is presented. Equivalent System Mass (ESM) comparisons are made of the existing TCCS systems with the carbon nanotube technology for removing NO(x). The potential for methane decomposition using carbon nanotubes catalysts is also discussed.

  15. Modeling of wormhole behavior in carbonate acidizing

    SciTech Connect

    Hung, K.M.

    1987-01-01

    A mathematical model that describes the growth and competition of wormholes during an acidizing treatment in a carbonate formation is developed. The purpose of the treatment is to remove any near wellbore permeability damage created by drilling or completion fluids so that the production of reservoir fluids is stimulated. Hydrochloric acid is commonly used for this purpose. Since the acid solution tends to flow into the less resistant areas, large pores on the rock surface receive most acid fluid. Pores are enlarged due to the reaction between acid solution and carbonates. The growth of large pores in the formation is referred to as wormholing. Results from the model show that wormholes are formed due to the heterogeneity of carbonate rock and the reaction kinetics between acid and carbonates. Formation of a dominant wormhole is controlled by fluid diffusivity and fluid loss. Model results have good agreement with the results from published papers.

  16. Method and apparatus for separating gases based on electrically and magnetically enhanced monolithic carbon fiber composite sorbents

    DOEpatents

    Judkins, Roddie R. (9917 Rainbow Dr., Knoxville, TN 37922); Burchell, Timothy D. (109 Greywood Pl., Oak Ridge, TN 37830)

    1999-01-01

    A method for separating gases or other fluids involves placing a magnetic field on a monolithic carbon fiber composite sorption material to more preferentially attract certain gases or other fluids to the sorption material to which a magnetic field is applied. This technique may be combined with the known "pressure swing adsorption" technique utilizing the same sorption material.

  17. Method and apparatus for separating gases based on electrically and magnetically enhanced monolithic carbon fiber composite sorbents

    DOEpatents

    Judkins, R.R.; Burchell, T.D.

    1999-07-20

    A method for separating gases or other fluids involves placing a magnetic field on a monolithic carbon fiber composite sorption material to more preferentially attract certain gases or other fluids to the sorption material to which a magnetic field is applied. This technique may be combined with the known pressure swing adsorption'' technique utilizing the same sorption material. 1 fig.

  18. Emission factors for particles, elemental carbon, and trace gases from the Kuwait oil fires

    SciTech Connect

    Laursen, K.K.; Ferek, R.J.; Hobbs, P.V.; Rasmussen, R.A.

    1992-09-20

    Emission factors are presented for particles, elemental carbon (i.e., soot), total organic carbon in particles and vapor, and for various trace gases from the 1991 Kuwait oil fires. Particle emissions accounted for {approximately} 2% of the fuel burned. In general, soot emission factors were substantially lower than those used in recent {open_quotes}nuclear winter{close_quotes} calculations. Differences in the emissions and appearances of some of the individual fires are discussed. Carbon budget data for the composite plumes from the Kuwait fires are summarized; most of the burned carbon in the plumes was in the form of CO{sub 2}. Fluxes are presented for several combustion products. 26 refs., 1 fig., 5 tabs.

  19. Soluble species in the Arctic summer troposphere - acidic gases, aerosols, and precipitation

    SciTech Connect

    Talbot, R.W.; Vijgen, A.S.; Harriss, R.C. Old Dominion Univ., Norfolk, VA )

    1992-10-01

    The large-scale spatial distribution from 0.15-to 6 km altitude in the North American Arctic troposphere of several soluble acidic gases and major aerosol species during the summertime is reported. The distribution is found to be compositionally consistent on a large spatial scale. The summertime troposphere is an acidic environment, with HCOOH and CH3COOH the principal acidic gases while acidic sulfate aerosols dominate the particulate phase. There appears to be a surface source of NH3 over the pack ice which may originate from decay of dead marine organisms on the ice surface, evolution from surface ocean waters in open ice leads, or release from rotting sea ice. At low altitude over the pack ice this NH34 appears to partially neutralize aerosol acidity. Over sub-Arctic tundra in southeastern Alaska, inputs of marine biogenic sulfur from the Bering Sea appear to be an important source of boundary layer aerosol SO4(2-). The rainwater acidity over the tundra is typical of remote regions. 61 refs.

  20. Soluble species in the Arctic summer troposphere - Acidic gases, aerosols, and precipitation

    NASA Technical Reports Server (NTRS)

    Talbot, R. W.; Vijgen, A. S.; Harriss, R. C.

    1992-01-01

    The large-scale spatial distribution from 0.15-to 6 km altitude in the North American Arctic troposphere of several soluble acidic gases and major aerosol species during the summertime is reported. The distribution is found to be compositionally consistent on a large spatial scale. The summertime troposphere is an acidic environment, with HCOOH and CH3COOH the principal acidic gases while acidic sulfate aerosols dominate the particulate phase. There appears to be a surface source of NH3 over the pack ice which may originate from decay of dead marine organisms on the ice surface, evolution from surface ocean waters in open ice leads, or release from rotting sea ice. At low altitude over the pack ice this NH34 appears to partially neutralize aerosol acidity. Over sub-Arctic tundra in southeastern Alaska, inputs of marine biogenic sulfur from the Bering Sea appear to be an important source of boundary layer aerosol SO4(2-). The rainwater acidity over the tundra is typical of remote regions.

  1. Adsorption and Dispersion of Selected Organic Gases Flowing Through Activated Carbon Adsorber Beds.

    NASA Astrophysics Data System (ADS)

    Forsythe, Robert Kenneth, Jr.

    An experimental investigation of the adsorption and dispersion of selected organic gases and vapors was performed for nominal 100-ppm concentrations of adsorptive in a helium carrier flowing through cylindrical adsorber beds containing Columbia 4LXC 12/28 activated carbon. The total pressure of the adsorptive and carrier gases was a nominal one atmosphere, and the temperature of the gas stream and adsorber bed was 25.0^circ C. The solid-phase concentration of adsorbate and the adsorption capacity were measured for the adsorptives methane, acetylene, ethane, methanol, acetaldehyde, propane, ethanol, acetone, Freon-113, and toluene. These parameters were determined from dynamic adsorption experiments with a mass-balance analysis of the breakthrough curves. The dimensionless adsorption capacity, defined as the ratio of the solid-phase concentration of adsorbate to the gas -phase concentration of adsorptive, ranged from 40.1 for methane to 6.71 times 10 ^5 for toluene. The adsorption isotherms for five of the selected gases on activated carbon were determined from dynamic adsorption experiments with input concentrations as high as 10,000 ppm. The isotherms encountered were linear, near-linear, and nonlinear; they could be represented by Langmuir and Chakravarti-Dhar theoretical functional forms. The isotherm of acetone was analyzed also with the Dubinin -Radushkevich equation and the Polanyi adsorption potential to predict the micropore volume of the carbon. The dispersion of the adsorptive gases was analyzed from the bed outlet concentration as a function of time. The diffusion coefficients for methane and acetylene were determined from the theories of the longitudinal- and homogeneous -solid-diffusion models. The effects of molecular, intraparticle, and eddy diffusion were measured and compared at various flow velocities. Input concentration boundary conditions included step-up and step-down functions, positive and negative rectangular pulses, positive and negative delta-function pulses, and up- and down-staircase functions.

  2. Raman Scattering Sensor for On-Line Monitoring of Amines and Acid Gases

    SciTech Connect

    Uibel, Rory; Smith, Lee

    2010-05-20

    Sulfur and CO2 removal from hydrocarbon streams and power plant effluents are a major problem. The sulfur is normally in the form of H2S. These two acid gases are scrubbed using aqueous amine solutions that are difficult to control with conventional technology. Process Instruments Inc. developed Raman scattering technology for on-line, real-time monitoring of amine streams to improve their efficiency in scrubbing H2S and CO2 from hydrocarbon streams and power plant effluents. Improved control of amine and acid gas concentrations will allow refineries, natural gas processes and power plants to more efficiently scrub Sulfur and CO2, saving energy, time and financial resources.

  3. Origin and migration of hydrocarbon gases and carbon dioxide, Bekes Basin, southeastern Hungary

    USGS Publications Warehouse

    Clayton, J.L.; Spencer, C.W.; Koncz, I.; Szalay, A.

    1990-01-01

    The Bekes Basin is a sub-basin within the Pannonian Basin, containing about 7000 m of post-Cretaceous sedimentary rocks. Natural gases are produced from reservoirs (Precambrian to Tertiary in age) located on structural highs around the margins of the basin. Gas composition and stable carbon isotopic data indicate that most of the flammable gases were derived from humic kerogen contained in source rocks located in the deep basin. The depth of gas generation and vertical migration distances were estimated using quantitative source rock maturity-carbon isotope relationships for methane compared to known Neogene source rock maturity-depth relationships in the basin. These calculations indicate that as much as 3500 m of vertical migration has occured in some cases. Isotopically heavy (> - 7 > 0) CO2 is the predominant species present in some shallow reservoirs located on basin-margin structural highs and has probably been derived via long-distance vertical and lateral migration from thermal decompositon of carbonate minerals in Mesozoic and older rocks in the deepest parts of the basin. A few shallow reservoirs (< 2000m) contain isotopically light (-50 to -60%0) methane with only minor amounts of C2+ homologs (< 3% v/v). This methane is probably mostly microbial in origin. Above-normal pressures, occuring at depths greater than 1800 m, are believed to be the principal driving force for lateral and vertical gas migration. These pressures are caused in part by active hydrocarbon generation, undercompaction, and thermal decomposition of carbonates

  4. Control of Effluent Gases from Solid Waste Processing using Impregnated Carbon Nanotubes

    NASA Technical Reports Server (NTRS)

    Li, Jing; Fisher, John; Wignarajah, Kanapathipillai

    2005-01-01

    One of the major problems associated with solid waste processing technologies is effluent contaminants that are released in gaseous forms from the processes. This is a concern in both biological as well as physicochemical solid waste processing. Carbon dioxide (CO2), the major gas released, does not present a serious problem and there are currently in place a number of flight-qualified technologies for CO2 removal. However, a number of other gases, in particular NOx, SO2, NH3, and various hydrocarbons (e.g. CH4) do present health hazards to the crew members in space habitats. In the present configuration of solid waste processing in the International Space Station (ISS), some of these gases are removed by the Trace Contaminant Control System (TCCS), demands a major resupply. Reduction of the resupply can be effective by using catalyst impregnated carbon nanotubes. For example, NO decomposition to N2 and O2 is thermodynamically favored. Data showing decomposition of NO on metal impregnated carbon nanotubes is presented. Comparisons are made of the existing TCCS systems with the carbon nanotube based technology for removing NOx based on mass/energy penalties.

  5. Effect of different carrier gases and their flow rates on the growth of carbon nanotubes

    NASA Astrophysics Data System (ADS)

    Tewari, Aarti; Sharma, Suresh C.

    2015-04-01

    The present paper examines the effect of different carrier gases and their flow rates on the growth of carbon nanotubes (CNTs). A theoretical model is developed incorporating the charging rate of the carbon nanotube, kinetics of all the plasma species, and the growth rate of the CNTs because of diffusion and accretion of ions on the catalyst nanoparticle. The three different carrier gases, i.e., argon (Ar), ammonia, and nitrogen, are considered in the present investigation, and flow rates of all the three carrier gases are varied individually (keeping the flow rates of hydrocarbon and hydrogen gas constant) to investigate the variations in the number densities of hydrocarbon and hydrogen ions in the plasma and their consequent effects on the height and radius of CNT. Based on the results obtained, it is concluded that Ar favors the formation of CNTs with larger height and radius whereas ammonia contributes to better height of CNT but decreases the radius of CNT, and nitrogen impedes both the height and radius of CNT. The present work can serve to the better understanding of process parameters during growth of CNTs by a plasma enhanced chemical vapor deposition process.

  6. Effect of different carrier gases and their flow rates on the growth of carbon nanotubes

    SciTech Connect

    Tewari, Aarti; Sharma, Suresh C.

    2015-04-15

    The present paper examines the effect of different carrier gases and their flow rates on the growth of carbon nanotubes (CNTs). A theoretical model is developed incorporating the charging rate of the carbon nanotube, kinetics of all the plasma species, and the growth rate of the CNTs because of diffusion and accretion of ions on the catalyst nanoparticle. The three different carrier gases, i.e., argon (Ar), ammonia, and nitrogen, are considered in the present investigation, and flow rates of all the three carrier gases are varied individually (keeping the flow rates of hydrocarbon and hydrogen gas constant) to investigate the variations in the number densities of hydrocarbon and hydrogen ions in the plasma and their consequent effects on the height and radius of CNT. Based on the results obtained, it is concluded that Ar favors the formation of CNTs with larger height and radius whereas ammonia contributes to better height of CNT but decreases the radius of CNT, and nitrogen impedes both the height and radius of CNT. The present work can serve to the better understanding of process parameters during growth of CNTs by a plasma enhanced chemical vapor deposition process.

  7. A death in a stationary vehicle whilst idling: unusual carbon monoxide poisoning by exhaust gases.

    PubMed

    Osawa, Motoki; Horiuchi, Hidekazu; Yoshida, Koutaro; Tada, Takeshi; Harada, Akira

    2003-03-01

    In this paper, we describe an autopsy case in which death was due to accidental carbon monoxide poisoning occurring in a stationary vehicle idling in an open space. To investigate the source of the fatal fumes, the death scene situation was reconstructed using the vehicle. Exhaust gases were found to invade the interior through the floor from a defective exhaust system. CO gas was detected while idling and the level in the cabin gradually rose to 1.5% over a 2-h period. Since the 8-year-old motor vehicle seemed to have been defective for some months, it was concluded that stationary idling overnight caused an accumulation of toxic gases in the interior. PMID:12935571

  8. Automatic carbon dioxide-methane gas sensor based on the solubility of gases in water.

    PubMed

    Cadena-Pereda, Ral O; Rivera-Muoz, Eric M; Herrera-Ruiz, Gilberto; Gomez-Melendez, Domingo J; Anaya-Rivera, Ely K

    2012-01-01

    Biogas methane content is a relevant variable in anaerobic digestion processing where knowledge of process kinetics or an early indicator of digester failure is needed. The contribution of this work is the development of a novel, simple and low cost automatic carbon dioxide-methane gas sensor based on the solubility of gases in water as the precursor of a sensor for biogas quality monitoring. The device described in this work was used for determining the composition of binary mixtures, such as carbon dioxide-methane, in the range of 0-100%. The design and implementation of a digital signal processor and control system into a low-cost Field Programmable Gate Array (FPGA) platform has permitted the successful application of data acquisition, data distribution and digital data processing, making the construction of a standalone carbon dioxide-methane gas sensor possible. PMID:23112626

  9. Automatic Carbon Dioxide-Methane Gas Sensor Based on the Solubility of Gases in Water

    PubMed Central

    Cadena-Pereda, Ral O.; Rivera-Muoz, Eric M.; Herrera-Ruiz, Gilberto; Gomez-Melendez, Domingo J.; Anaya-Rivera, Ely K.

    2012-01-01

    Biogas methane content is a relevant variable in anaerobic digestion processing where knowledge of process kinetics or an early indicator of digester failure is needed. The contribution of this work is the development of a novel, simple and low cost automatic carbon dioxide-methane gas sensor based on the solubility of gases in water as the precursor of a sensor for biogas quality monitoring. The device described in this work was used for determining the composition of binary mixtures, such as carbon dioxide-methane, in the range of 0100%. The design and implementation of a digital signal processor and control system into a low-cost Field Programmable Gate Array (FPGA) platform has permitted the successful application of data acquisition, data distribution and digital data processing, making the construction of a standalone carbon dioxide-methane gas sensor possible. PMID:23112626

  10. Utilization of carbon dioxide in industrial flue gases for the cultivation of microalga Chlorella sp.

    PubMed

    Kao, Chien-Ya; Chen, Tsai-Yu; Chang, Yu-Bin; Chiu, Tzai-Wen; Lin, Hsiun-Yu; Chen, Chun-Da; Chang, Jo-Shu; Lin, Chih-Sheng

    2014-08-01

    The biomass and lipid productivity of Chlorella sp. MTF-15 cultivated using aeration with flue gases from a coke oven, hot stove or power plant in a steel plant of the China Steel Corporation in Taiwan were investigated. Using the flue gas from the coke oven, hot stove or power plant for cultivation, the microalgal strain obtained a maximum specific growth rate and lipid production of (0.827 d(-1), 0.688 g L(-1)), (0.762 d(-1), 0.961 g L(-1)), and (0.728 d(-1), 0.792 g L(-1)), respectively. This study demonstrated that Chlorella sp. MTF-15 could efficiently utilize the CO₂, NOX and SO₂ present in the different flue gases. The results also showed that the growth potential, lipid production and fatty acid composition of the microalgal strain were dependent on the composition of the flue gas and on the operating strategy deployed. PMID:24950094

  11. Evaluation of the drag force on single-walled carbon nanotubes in rarefied gases.

    PubMed

    Wong, Ross Y M; Liu, Chong; Wang, Jun; Chao, Christopher Y H; Li, Zhigang

    2012-03-01

    The drag force on carbon nanotubes (CNTs) in dilute gases has been previously derived. However, the drag force formulae involve collision integrals, which are complex functions of the gas-CNT interaction potential. The unavailability of the collision integrals and interaction potential makes the application of the theoretical drag force laws impossible. In this work, we develop a potential model for the interaction between a gas and single-walled CNT. The collision integrals are then calculated based on the potential and empirical expressions are proposed. Finally, the drag force is computed directly through molecular dynamics simulations and compared with the theoretical predictions. PMID:22755052

  12. Laboratory simulation of meteoritic noble gases. III - Sorption of neon, argon, krypton, and xenon on carbon - Elemental fractionation

    NASA Technical Reports Server (NTRS)

    Wacker, John F.

    1989-01-01

    The sorption of Ne, Ar, Kr, and Xe was studied in carbon black, acridine carbon, and diamond in an attempt to understand the origin of trapped noble gases in meteorites. The results support a model in which gases are physically adsorbed on interior surfaces formed by a pore labyrinth within amorphous carbons. The data show that: (1) the adsorption/desorption times are controlled by choke points that restrict the movement of noble gas atoms within the pore labyrinth, and (2) the physical adsorption controls the temperature behavior and elemental fractionation patterns.

  13. Laboratory simulation of meteoritic noble gases. I - Sorption of xenon on carbon: Trapping experiments

    NASA Astrophysics Data System (ADS)

    Wacker, J. F.; Zadnik, M. G.; Anders, E.

    1985-04-01

    The sorption of Xe-127 at 5 x 10 to the -7th atm onto carbon black, pyrolyzed polyvinylidene chloride, and pyrolyzed acridine at 100-1000 C for 5 min-240 h is measured experimentally by gamma spectrometry. The results are presented in tables and graphs and characterized in detail. The tightly bound Xe remaining in the samples after 4000 min pumping at temperatures above 100 C is found to comprise two components: a low-temperature component attributed to physisorption within an atomic-scale labyrinth of micropores, and a high-temperature component due to volume diffusion. The implications for the trapping of noble gases near grain surfaces of amorphous carbon in meteorites are considered.

  14. Laboratory simulation of meteoritic noble gases. I - Sorption of xenon on carbon: Trapping experiments

    NASA Technical Reports Server (NTRS)

    Wacker, J. F.; Zadnik, M. G.; Anders, E.

    1985-01-01

    The sorption of Xe-127 at 5 x 10 to the -7th atm onto carbon black, pyrolyzed polyvinylidene chloride, and pyrolyzed acridine at 100-1000 C for 5 min-240 h is measured experimentally by gamma spectrometry. The results are presented in tables and graphs and characterized in detail. The tightly bound Xe remaining in the samples after 4000 min pumping at temperatures above 100 C is found to comprise two components: a low-temperature component attributed to physisorption within an atomic-scale labyrinth of micropores, and a high-temperature component due to volume diffusion. The implications for the trapping of noble gases near grain surfaces of amorphous carbon in meteorites are considered.

  15. Analysis of Effluent Gases During the CCVD Growth of Multi Wall Carbon Nanotubes from Acetylene

    NASA Technical Reports Server (NTRS)

    Schmitt, T. C.; Biris, A. S.; Miller, D. W.; Biris, A. R.; Lupu, D.; Trigwell, S.; Rahman, Z. U.

    2005-01-01

    Catalytic chemical vapor deposition was used to grow multi-walled carbon nanotubes on a Fe:Co:CaCO3 catalyst from acetylene. The influent and effluent gases were analyzed by gas chromatography and mass spectrometry at different time intervals during the nanotubes growth process in order to better understand and optimize the overall reaction. A large number of byproducts were identified and it was found that the number and the level for some of the carbon byproducts significantly increased over time. The CaCO3 catalytic support thermally decomposed into CaO and CO2 resulting in a mixture of two catalysts for growing the nanotubes, which were found to have outer diameters belonging to two main groups 8 to 35 nm and 40 to 60 nm, respectively.

  16. Molecular dynamics simulation of diffusion of gases in a carbon-nanotube-polymer composite

    SciTech Connect

    Lim, Seong Y.; Sahimi, Muhammad; Tsotsis, Theodore T.; Kim, Nayong

    2007-07-15

    Extensive molecular dynamics (MD) simulations were carried out to compute the solubilities and self-diffusivities of CO{sub 2} and CH{sub 4} in amorphous polyetherimide (PEI) and mixed-matrix PEI generated by inserting single-walled carbon nanotubes into the polymer. Atomistic models of PEI and its composites were generated using energy minimizations, MD simulations, and the polymer-consistent force field. Two types of polymer composite were generated by inserting (7,0) and (12,0) zigzag carbon nanotubes into the PEI structure. The morphologies of PEI and its composites were characterized by their densities, radial distribution functions, and the accessible free volumes, which were computed with probe molecules of different sizes. The distributions of the cavity volumes were computed using the Voronoi tessellation method. The computed self-diffusivities of the gases in the polymer composites are much larger than those in pure PEI. We find, however, that the increase is not due to diffusion of the gases through the nanotubes which have smooth energy surfaces and, therefore, provide fast transport paths. Instead, the MD simulations indicate a squeezing effect of the nanotubes on the polymer matrix that changes the composite polymers' free-volume distributions and makes them more sharply peaked. The presence of nanotubes also creates several cavities with large volumes that give rise to larger diffusivities in the polymer composites. This effect is due to the repulsive interactions between the polymer and the nanotubes. The solubilities of the gases in the polymer composites are also larger than those in pure PEI, hence indicating larger gas permeabilities for mixed-matrix PEI than PEI itself.

  17. Noble Gases and Nitrogen Released from a Lunar Soil Pyroxene Separate by Acid Etching

    NASA Astrophysics Data System (ADS)

    Rider, P. E.

    1993-07-01

    We report initial results from a series of experiments designed to measure recently implanted solar wind (SW) ions in lunar soil mineral grains [1]. An acid-etching technique similar to the CSSE method developed at ETH Zurich was used to make abundance and isotope measurements of the SW noble gas and nitrogen compositions. Among the samples examined was a pyroxene separate from soil 75081. It was first washed with H2O to remove contamination from the sample finger walls and grain surfaces. H2O also acted as a weak acid, releasing gases from near-surface sites. Treatment with H2SO3 followed the water washes. Acid pH (~1.8 to ~1.0) and temperature (~23 degrees C to ~90 degrees C) and duration of acid attack (several minutes to several days) were varied from step to step. Finally, the sample was pyrolyzed in several steps to remove the remaining gases, culminating with a high-temperature pyrolysis at 1200 degrees C. Measurements of the light noble gases were mostly consistent with those from previous CSSE experiments performed on pyroxene [2,3]. It should be noted, however, that the Zurich SEP component was not easily distinguishable in the steps where it was expected to be observed. We suspect our experimental protocol masked the SEP reservoir, preventing us from seeing its distinctive signature. The most interesting results from this sample are its Kr and Xe isotopic and elemental compositions. Pyroxene apparently retains heavy noble gases as well as ilmenite (and plagioclase [4]). The heavy noble gas element ratios from this sample along with those previously reported [5,6] are, however, considerably heavier than the theoretically determined "solar system" values [7,8]. Explanations for the difference include the possibility that the derivations are incorrect, that there is another component of lunar origin mixing with the solar component, or that some type of loss mechanism is altering the noble gas reservoirs of the grains. The Kr and Xe isotopic compositions for the two acid-etch steps most likely to have released SW gases were identical to the "solar" values reported by the Zurich group [5]. The krypton from both steps appeared to be mixtures of "solar" krypton, an isotopically heavier component (perhaps the Zurich SEP component [5]), and a spallation component. There was, however, no evidence for such a mixture in the xenon. The compositions of the two acid-etch steps were clearly combinations of a solar Xe component and a Xe spallation component. They were also identical to that of U-Xe [9] for isotopes up to 132Xe, with the exception of an ~300 per mil enhancement of the 126Xe/132Xe ratio. This anomaly does not appear to be an artifact of spallation correction. These measurements constitute the first experimental verification of the U-Xe composition for isotopes lighter than 134Xe. Persistent contamination problems and the possibility of nitrogen being held back in the acid residue during the etching process make interpretation of the nitrogen data uncertain. However, results from the steps not obviously affected by contamination show an enhancement of N over Ar by 2x to 12x the "solar" value (from [8]). References: [1] Rider P. E. and Pepin R. O. (1993) GCA, submitted. [2] Wieler R. et al. (1986) GCA, 50, 1997-2017. [3] Benkert J.-P. (1989) Ph.D. thesis, ETH Zurich (No. 8812). [4] Wieler R. (1993) personal communication. [5] Wieler R. et al. (1992) LPS XXIII, 1525-1526. [6] Wieler R. et al. (1993) LPS XXIV, 1519-1520. [7] Anders E. and Grevesse N. (1989) GCA, 53, 197-214. [8] Cameron A. G. W. (1982) In Essays in Nuclear Physics (Barnes et al., eds.), 23-43. [9] Pepin R. O.(1991) Icarus, 92, 2-79.

  18. Synthesis of carbon-13-labeled tetradecanoic acids.

    PubMed

    Sparrow, J T; Patel, K M; Morrisett, J D

    1983-07-01

    The synthesis of tetradecanoic acid enriched with 13C at carbons 1, 3, or 6 is described. The label at the carbonyl carbon was introduced by treating 1-bromotridecane with K13CN (90% enriched) to form the 13C-labeled nitrile, which upon hydrolysis yielded the desired acid. The [3-13C]tetradecanoic acid was synthesized by alkylation of diethyl sodio-malonate with [1-13C]1-bromododecane; the acid was obtained upon saponification and decarboxylation. The label at the 6 position was introduced by coupling the appropriately labeled alkylcadmium chloride with the half acid chloride methyl ester of the appropriate dioic acid, giving the corresponding oxo fatty acid ester. Formation of the tosylhydrazone of the oxo-ester followed by reduction with sodium cyanoborohydride gave the labeled methyl tetradecanoate which, upon hydrolysis, yielded the desired tetradecanoic acid. All tetradecanoic acids were identical to unlabeled analogs as evaluated by gas-liquid chromatography and infrared or NMR spectroscopy. These labeled fatty acids were used subsequently to prepare the correspondingly labeled diacyl phosphatidylcholines. PMID:6631228

  19. Measurement and analysis of the relationship between ammonia, acid gases, and fine particles in eastern North Carolina.

    PubMed

    Baek, Bok Haeng; Aneja, Viney P

    2004-05-01

    An annular denuder system, which consisted of a cyclone separator; two diffusion denuders coated with sodium carbonate and citric acid, respectively; and a filter pack consisting of Teflon and nylon filters in series, was used to measure acid gases, ammonia (NH3), and fine particles in the atmosphere from April 1998 to March 1999 in eastern North Carolina (i.e., an NH3-rich environment). The sodium carbonate denuders yielded average acid gas concentrations of 0.23 microg/m3 hydrochloric acid (standard deviation [SD] +/- 0.2 microg/m3); 1.14 microg/m3 nitric acid (SD +/- 0.81 microg/m3), and 1.61 microg/m3 sulfuric acid (SD +/- 1.58 microg/m3). The citric acid denuders yielded an average concentration of 17.89 microg/m3 NH3 (SD +/- 15.03 microg/m3). The filters yielded average fine aerosol concentrations of 1.64 microg/m3 ammonium (NH4+; SD +/- 1.26 microg/m3); 0.26 microg/m3 chloride (SD +/- 0.69 microg/m3), 1.92 microg/m3 nitrate (SD +/- 1.09 microg/m3), and 3.18 microg/m3 sulfate (SO4(2-); SD +/- 3.12 microg/m3). From seasonal variation, the measured particulates (NH4+, SO4(2-), and nitrate) showed larger peak concentrations during summer, suggesting that the gas-to-particle conversion was efficient during summer. The aerosol fraction in this study area indicated the domination of ammonium sulfate particles because of the local abundance of NH3, and the long-range transport of SO4(2-) based on back trajectory analysis. Relative humidity effects on gas-to-particle conversion processes were analyzed by particulate NH4+ concentration originally formed from the neutralization processes with the secondary pollutants in the atmosphere. PMID:15149049

  20. Synergistic effect of Brnsted acid and platinum on purification of automobile exhaust gases

    NASA Astrophysics Data System (ADS)

    Fu, Wei; Li, Xin-Hao; Bao, Hong-Liang; Wang, Kai-Xue; Wei, Xiao; Cai, Yi-Yu; Chen, Jie-Sheng

    2013-08-01

    The catalytic purification of automobile exhaust gases (CO, NOx and hydrocarbons) is one of the most practiced conversion processes used to lower the emissions and to reduce the air pollution. Nevertheless, the good performance of exhaust gas purification catalysts often requires the high consumption of noble metals such as platinum. Here we report that the Brnsted acid sites on the external surface of a microporous silicoaluminophosphate (SAPO) act as a promoter for exhaust gas purification, effectively cutting the loading amount of platinum in the catalyst without sacrifice of performance. It is revealed that in the Pt-loaded SAPO-CHA catalyst, there exists a remarkable synergistic effect between the Brnsted acid sites and the Pt nanoparticles, the former helping to adsorb and activate the hydrocarbon molecules for NO reduction during the catalytic process. The thermal stability of SAPO-CHA also makes the composite catalyst stable and reusable without activity decay.

  1. Synergistic effect of Brnsted acid and platinum on purification of automobile exhaust gases

    PubMed Central

    Fu, Wei; Li, Xin-Hao; Bao, Hong-Liang; Wang, Kai-Xue; Wei, Xiao; Cai, Yi-Yu; Chen, Jie-Sheng

    2013-01-01

    The catalytic purification of automobile exhaust gases (CO, NOx and hydrocarbons) is one of the most practiced conversion processes used to lower the emissions and to reduce the air pollution. Nevertheless, the good performance of exhaust gas purification catalysts often requires the high consumption of noble metals such as platinum. Here we report that the Brnsted acid sites on the external surface of a microporous silicoaluminophosphate (SAPO) act as a promoter for exhaust gas purification, effectively cutting the loading amount of platinum in the catalyst without sacrifice of performance. It is revealed that in the Pt-loaded SAPO-CHA catalyst, there exists a remarkable synergistic effect between the Brnsted acid sites and the Pt nanoparticles, the former helping to adsorb and activate the hydrocarbon molecules for NO reduction during the catalytic process. The thermal stability of SAPO-CHA also makes the composite catalyst stable and reusable without activity decay. PMID:23907148

  2. Adsorption of Single and Binary Gases on Polystyrene and Carbon Adsorbents

    NASA Astrophysics Data System (ADS)

    Rothstein, Daniel P.

    Time-dependent transmissions of light organic gases at low concentrations through crosslinked polystyrene and activated carbon adsorbents were measured and analyzed to extract kinetic and equilibrium parameters and to evaluate these parameters in terms of several models of adsorption. Mass -balance in the adsorber bed allows calculation of the equilibrium adsorbed-phase concentration and the model-independent adsorption capacity. Adsorption isotherms are calculated from transmission curves for eight light organic gases adsorbed on polystyrene at several temperatures. The power-law forms of the Freundlich and Chakravarti-Dhar isotherms and the concentration-dependent adsorption capacities indicate heterogeneous adsorption well below monolayer coverage. The effects of heterogeneity increase as non-linearity of the isotherm increases. A mesopore structure is indicated for polystyrene. Characteristic curves are independent of temperature, but the use of an affinity coefficient is not able to demonstrate their independence of adsorbate. Isosteric hearts of adsorption are larger than the heats of vaporization and decrease with increasing surface coverage for three alkanes adsorbed on polystyrene. The transmission curves of several binary mixtures of gases with non-linear isotherms reveal adsorption interference, with adsorption capacities smaller than those from single -component experiments. The pairs with unequal adsorption capacities exhibit displacement, in qualitative agreement with adsorption interference models. The equilibrium adsorption of the binary mixtures cannot be reproduced by single-component isotherm parameters alone, but are described by modified Freundlich isotherms requiring binary experiments. Adsorption in a porous medium is described by a model including four dynamic processes: gas- and solid -phase diffusion, interfacial mass-transfer resistance, and a first-order chemical reaction. A new time-dependent solution to the differential equations of adsorption with linear isotherms for a step increase in the input concentration is an infinite series of integrals which must be evaluated numerically. The moments of the solution for both step and rectangular-pulse input yield expressions for the kinetic parameters, which are evaluated from the data for several gases with nearly-linear isotherms. The asymptotic concentration profile is utilized to calculate diffusion coefficients for several gases with non-linear isotherms and to generate a non-linear isotherm from a single transmission curve.

  3. Oceanic Trace Gases Numeric Data Packages from the Carbon Dioxide Information Analysis Center (CDIAC)

    DOE Data Explorer

    CDIAC products include numeric data packages, publications, trend data, atlases, models, etc. and can be searched for by subject area, keywords, authors, product numbers, time periods, collection sites, spatial references, etc. Most data sets or packages, many with numerous data files, are free to download from CDIAC's ftp area. CDIAC lists the following numeric data packages under the broad heading of Oceanic Trace Gases: Carbon Dioxide, Hydrographic, and Chemical Data Obtained during the R/V Ronald H. Brown Repeat Hydrography Cruise in the Atlantic Ocean: CLIVAR CO2 Section A16S_2005 ( 01/11/05 - 022405) • Determination of Carbon Dioxide, Hydrographic, and Chemical Parameters during the R/V Nathaniel B. Palmer Cruise in the Southern Indian Ocean (WOCE Section S04I, 050396 - 070496) • Inorganic Carbon, Nutrient, and Oxygen Data from the R/V Ronald H. Brown Repeat Hydrography Cruise in the Atlantic Ocean: CLIVAR CO2 Section A16N_2003a (060403 – 081103) • Carbon Dioxide, Hydrographic, and Chemical Data Obtained During the R/V Maurice Ewing Cruise in the Atlantic Ocean (WOCE Section A17, 010494 - 032194) • Global Ocean Data Analysis Project GLODAP: Results and Data • Carbon Dioxide, Hydrographic, and Chemical Data Obtained During the R/V Knorr Cruises in the North Atlantic Ocean on WOCE Sections AR24 (1102 – 120596) and A24, A20, and A22 (053097 – 090397) • Carbon Dioxide, Hydrographic and Chemical Data Obtained During the Nine R/V Knorr Cruises Comprising the Indian Ocean CO2 Survey (WOCE Sections I8SI9S, I9N, I8NI5E, I3, I5WI4, I7N, I1, I10, and I2; 120 194 – 012296) • Carbon Dioxide, Hydrographic, and Chemical Data Obtained During the R/V Meteor Cruise 28/1 in the South Atlantic Ocean (WOCE Section A8, 032994 - 051294) • Carbon Dioxide, Hydrographic, and Chemical Data Obtained During the R/V Knorr Cruise 138-3, -4, and -5 in the South Pacific Ocean (WOCE Sections P6E, P6C, and P6W, 050292 - 073092) • Global Distribution of Total Inorganic Carbon and Total Alkalinity below the deepest winter mixed layer depths • Carbon Dioxide, Hydrographic, and Chemical Data Obtained During the R/V John V. Vickers Cruise in the Pacific Ocean (WOCE Section P13, NOAA CGC92 Cruise, 080492 – 102192) • Carbon Dioxide, Hydrographic, and Chemical Data Obtained During the R/V Hesperides Cruise in the Atlantic Ocean (WOCE Section A5, 071492 - 081592) • Carbon Dioxide, Hydrographic, and Chemical Data Obtained During the R/V Thomas G. Thompson Cruise in the Pacific Ocean (WOCE Section P10, 100593 – 111093) • The International Intercomparison Exercise of Underway fCO2 Systems during the R/V Meteor Cruise 36/1 in the North Atlantic Ocean • Carbon Dioxide, Hydrographic, and Chemical Data Obtained during the R/V Meteor Cruise 22/5 in the South Atlantic Ocean (WOCE Section A10, Dec. 1992-Jan, 1993) • Carbon Dioxide, Hydrographic, and Chemical Data Obtained in the South Pacific Ocean (WOCE Sections P16A/P17A, P17E/P19S, and P19C, R/V Knorr , Oct. 1992-April 1993) • Surface Water and Atmospheric Underway Carbon Data Obtained During the World Ocean Circulation Experiment Indian Ocean Survey Cruises (R/V Knorr, Dec. 1994 – Jan, 1996) • Carbon Dioxide, Hydrographic, and Chemical Data Obtained During the R/V Akademik Ioffe Cruise in the South Pacific Ocean (WOCE Section S4P, Feb.-April 1992) • Carbon Dioxide, Hydrographic, and Chemical Data Obtained During the R/V Thomas Washington Cruise TUNES-1 in the Equatorial Pacific Ocean (WOCE section P17C) • Carbon Dioxide, Hydrographic, and Chemical Data Obtained During the R/V Thomas Washington Cruise TUNES-3 in the Equatorial Pacific Ocean (WOCE section P16C) • Carbon-14 Measurements in Surface Water CO2 from the Atlantic, Indian and Pacific Oceans, 1965-1994 • Carbon Dioxide, Hydrographic, and Chemical Data Obtained During R/V Meteor Cruise 18/1 in the North Atlantic Ocean (WOCE Section A1E) • Carbon Dioxide, Hydrographic, and Chemical Data Obtained in the Central South Pacific Ocean (WOCE Sections P17S and P16S) during the TUNES-2 Expedition of the R/V Thomas Washington, July-August, 1991 • Total Carbon Dioxide, Hydrographic, and Nitrate Measurements in the Southwest Pacific during Austral Autumn, 1990: Results from NOAA/PMEL CGC-90 Cruise • Carbon Dioxide, Hydrographic, and Chemical Data Obtained During the R/V Meteor Cruise 15/3 in the South Atlantic Ocean (WOCE Section A9, February March 1991) • Carbon Dioxide Concentrations in Surface Water and the Atmosphere During 1986-1989 NOAA/PMEL Cruises in the Pacific and Indian Oceans • Carbon Dioxide, Hydrographic, and Chemical Data Obtained During the R/V Meteor Cruise 11/5 in the South Atlantic and Northern Weddell Sea Areas (WOCE sections A-12 and A-21) • Surface Water and Atmospheric Carbon Dioxide and Nitrous Oxide Observations by Shipboard Automated Gas Chromatography: Results from Expeditions Between 1977 and 1990 • Indian Ocean Radiocarbon: Data from the INDIGO 1, 2, and 3 Cruises • Carbonate Chemistry of the North Pacific Ocean • Carbonate Chemistry of the Weddell Sea • GEOSECS Atlantic, Pacific, Indian, and Mediterranean Radiocarbon Data •\tTransient Tracers in the Oceans (TTO) - Hydrographic Data and Carbon Dioxide Systems with Revised Carbon Chemistry Data.

  4. Combustion systems and power plants incorporating parallel carbon dioxide capture and sweep-based membrane separation units to remove carbon dioxide from combustion gases

    DOEpatents

    Wijmans, Johannes G.; Merkel, Timothy C; Baker, Richard W.

    2011-10-11

    Disclosed herein are combustion systems and power plants that incorporate sweep-based membrane separation units to remove carbon dioxide from combustion gases. In its most basic embodiment, the invention is a combustion system that includes three discrete units: a combustion unit, a carbon dioxide capture unit, and a sweep-based membrane separation unit. In a preferred embodiment, the invention is a power plant including a combustion unit, a power generation system, a carbon dioxide capture unit, and a sweep-based membrane separation unit. In both of these embodiments, the carbon dioxide capture unit and the sweep-based membrane separation unit are configured to be operated in parallel, by which we mean that each unit is adapted to receive exhaust gases from the combustion unit without such gases first passing through the other unit.

  5. Greenhouse gases, climate change and the transition from coal to low-carbon electricity

    NASA Astrophysics Data System (ADS)

    Myhrvold, N. P.; Caldeira, K.

    2012-03-01

    A transition from the global system of coal-based electricity generation to low-greenhouse-gas-emission energy technologies is required to mitigate climate change in the long term. The use of current infrastructure to build this new low-emission system necessitates additional emissions of greenhouse gases, and the coal-based infrastructure will continue to emit substantial amounts of greenhouse gases as it is phased out. Furthermore, ocean thermal inertia delays the climate benefits of emissions reductions. By constructing a quantitative model of energy system transitions that includes life-cycle emissions and the central physics of greenhouse warming, we estimate the global warming expected to occur as a result of build-outs of new energy technologies ranging from 100 GWe to 10 TWe in size and 1-100 yr in duration. We show that rapid deployment of low-emission energy systems can do little to diminish the climate impacts in the first half of this century. Conservation, wind, solar, nuclear power, and possibly carbon capture and storage appear to be able to achieve substantial climate benefits in the second half of this century; however, natural gas cannot.

  6. Water-responsive carbon nanotubes for selective detection of toxic gases

    NASA Astrophysics Data System (ADS)

    Mukherjee, Soumalya; Sakorikar, Tushar; Mukherjee, Anwesha; Misra, Abha

    2015-03-01

    Ammonia plays an important role in our daily lives and hence its quantitative and qualitative sensing has become necessary. Bulk structure of carbon nanotubes (CNTs) has been employed to detect the gas concentration of 10 ppm. Hydrophobic CNTs were turned to hydrophilic via the application of a ramp electric field that allowed confinement of a controlled amount of water inside CNT microstructure. These samples were then also used to detect different gases. A comparative study has been performed for sensing three reducing gases, namely, ammonia, sulphur-di-oxide, and hydrogen sulphide to elaborate the selectivity of the sensor. A considerable structural bending in the bulk CNT was observed on evaporation of the confined water, which can be accounted to the zipping of individual nanotubes. However, the rate of the stress induced on these bulk microstructures increased on the exposure of ammonia due to the change in the surface tension of the confined solvent. A prototype of an alarm system has been developed to illustrate sensing concept, wherein the generated stress in the bulk CNT induces a reversible loss in electrical contact that changes the equivalent resistance of the electrical circuit upon exposure to the gas.

  7. Estimated flows of gases and carbon within CEEF ecosystem composed of human, crops and goats

    NASA Astrophysics Data System (ADS)

    Tako, Y.; Komatsubara, O.; Honda, G.; Arai, R.; Nitta, K.

    The Closed Ecology Experiment Facilities (CEEF) can be used as a test bed for Controlled Ecological Life Support Systems (CELSS), because technologies developed for the CEEF system facilitate self-sufficient material circulation necessary for long term missions such as Lunar and Mars exploration. In the experiment conducted under closed condition in FY2003, rice and soybeans were cultivated sequentially in two chambers and a chamber, each having a cultivation area of 30 m2 and floor area of 43 m2, inside the Plantation Module with artificial lighting of the CEEF. In the chamber having a cultivation area of 60 m2 and floor area of 65 m2, inside the Plantation Module with natural and artificial lighting, peanuts and safflowers were also cultivated. Stable transplant (or seeding) and harvest of each crop were maintained during a month. Flows of CO2, O2 and carbon to and from the crops were analyzed during the stable cultivation period. Simulated works and stay in the CEEF lasting five days were conducted two times under ventilating condition in FY2003. Gas exchange of human was estimated using heart rate data collected during the experiments and correlation between gas exchange rate and heart rate. Gas exchange rate and carbon balance of female goats were determined using an open-flow measurement system with a gastight chamber. From these results, flows of gases and carbon in the CEEF were discussed.

  8. Effect of gases on the temperature dependence of the electric conductivity of CVD multiwalled carbon nanotubes

    SciTech Connect

    Buryakov, T. I. Romanenko, A. I.; Anikeeva, O. B.; Kuznetsov, V. L.; Usol'tseva, A. N.; Tkachev, E. N.

    2007-07-15

    The influence of various gaseous media on the temperature dependence of the electric conductivity {sigma} of multiwalled carbon nanotubes (MWNTs) synthesized using the method of catalytical chemical vapor deposition (CVD) has been studied. The {sigma}(T) curves were measured in a temperature range from 4.2 to 300 K in helium and its mixtures with air, methane, oxygen, and hydrogen. The introduction of various gaseous components into a helium atmosphere leads to a significant decrease in the conductivity of MWNTs in the interval between the temperatures of condensation and melting of the corresponding gas. Upon a heating-cooling cycle, the conductivity restores on the initial level. It is concluded that a decrease in {sigma} is caused by the adsorption of gases on the surface of nanotubes.

  9. Carbon Dioxide Separation from Flue Gases: A Technological Review Emphasizing Reduction in Greenhouse Gas Emissions

    PubMed Central

    Songolzadeh, Mohammad; Soleimani, Mansooreh; Takht Ravanchi, Maryam; Songolzadeh, Reza

    2014-01-01

    Increasing concentrations of greenhouse gases (GHGs) such as CO2 in the atmosphere is a global warming. Human activities are a major cause of increased CO2 concentration in atmosphere, as in recent decade, two-third of greenhouse effect was caused by human activities. Carbon capture and storage (CCS) is a major strategy that can be used to reduce GHGs emission. There are three methods for CCS: pre-combustion capture, oxy-fuel process, and post-combustion capture. Among them, post-combustion capture is the most important one because it offers flexibility and it can be easily added to the operational units. Various technologies are used for CO2 capture, some of them include: absorption, adsorption, cryogenic distillation, and membrane separation. In this paper, various technologies for post-combustion are compared and the best condition for using each technology is identified. PMID:24696663

  10. Carbon dioxide separation from flue gases: a technological review emphasizing reduction in greenhouse gas emissions.

    PubMed

    Songolzadeh, Mohammad; Soleimani, Mansooreh; Takht Ravanchi, Maryam; Songolzadeh, Reza

    2014-01-01

    Increasing concentrations of greenhouse gases (GHGs) such as CO2 in the atmosphere is a global warming. Human activities are a major cause of increased CO2 concentration in atmosphere, as in recent decade, two-third of greenhouse effect was caused by human activities. Carbon capture and storage (CCS) is a major strategy that can be used to reduce GHGs emission. There are three methods for CCS: pre-combustion capture, oxy-fuel process, and post-combustion capture. Among them, post-combustion capture is the most important one because it offers flexibility and it can be easily added to the operational units. Various technologies are used for CO2 capture, some of them include: absorption, adsorption, cryogenic distillation, and membrane separation. In this paper, various technologies for post-combustion are compared and the best condition for using each technology is identified. PMID:24696663

  11. Foliage plants for indoor removal of the primary combustion gases carbon monoxide and nitrogen dioxide

    NASA Technical Reports Server (NTRS)

    Wolverton, B. C.; Mcdonald, R. C.; Mesick, H. H.

    1985-01-01

    Foliage plants were evaluated for their ability to sorb carbon monoxide and nitrogen dioxide, the two primary gases produced during the combustion of fossil fuels and tobacco. The spider plant (Chlorophytum elatum var. vittatum) could sorb 2.86 micrograms CO/sq cm leaf surface in a 6 h photoperiod. The golden pothos (Scindapsus aureus) sorbed 0.98 micrograms CO/sq cm leaf surface in the same time period. In a system with the spider plant, greater than or equal to 99 percent of an initial concentration of 47 ppm NO2 could be removed in 6 h from a void volume of approximately 0.35 cu m. One spider plant potted in a 3.8 liter container can sorb 3300 micrograms CO and effect the removal of 8500 micrograms NO2/hour, recognizing the fact that a significant fraction of NO2 at high concentrations will be lost by surface sorption, dissolving in moisture, etc.

  12. Carbon Dioxide Information Analysis Center and World Data Center for Atmospheric Trace Gases, Fiscal Year 2002 Annual Report

    SciTech Connect

    Cushman, R.M.

    2003-08-28

    The Carbon Dioxide Information Analysis Center (CDIAC), which includes the World Data Center (WDC) for Atmospheric Trace Gases, is the primary global change data and information analysis center of the U.S. Department of Energy (DOE). More than just an archive of data sets and publications, CDIAC has, since its inception in 1982, enhanced the value of its holdings through intensive quality assurance, documentation, and integration. Whereas many traditional data centers are discipline-based (for example, meteorology or oceanography), CDIAC's scope includes potentially anything and everything that would be of value to users concerned with the greenhouse effect and global climate change, including atmospheric concentrations and atmospheric emissions of carbon dioxide (CO{sub 2}) and other radiatively active gases; the role of the terrestrial biosphere and the oceans in the biogeochemical cycles of greenhouse gases; long-term climate trends; the effects of elevated CO{sub 2} on vegetation; and the vulnerability of coastal areas to rising sea levels.

  13. Carbon dioxide Information Analysis Center and World Data Center: A for Atmospheric trace gases. Annual progress report, FY 1994

    SciTech Connect

    Burtis, M.D.; Cushman, R.M.; Boden, T.A.; Jones, S.B.; Nelson, T.R.; Stoss, F.W.

    1995-03-01

    This report summarizes the activities and accomplishments made by the Carbon Dioxide Information Analysis Center and World Data Center-A for Atmospheric Trace Gases during the fiscal year 1994. Topics discussed in this report include; organization and staff, user services, systems, communications, Collaborative efforts with China, networking, ocean data and activities of the World Data Center-A.

  14. Oral drug delivery of therapeutic gases - carbon monoxide release for gastrointestinal diseases.

    PubMed

    Steiger, Christoph; Lühmann, Tessa; Meinel, Lorenz

    2014-09-10

    Deploying the therapeutic potential of carbon monoxide (CO) in various gastrointestinal diseases is challenged by inappropriate oral delivery modes. It is for this challenge, that we developed an easy to use tablet referred to as oral carbon monoxide release system (OCORS) providing precise, controlled, tunable and targeted CO delivery for the treatment of sequelae of gastrointestinal diseases. OCORS is an oral tablet based on sulfite induced CO release from the CO releasing molecule 2 (CORM-2). OCORS performance was detailed as a function of the presence of buffer within the tablet core and the composition of a semipermeable cellulose acetate coating, shielding the tablet core. OCORS delivered CO for up to 10h with a nearly linear release profile between approximately 30 to 240min. This controlled release system delivered the therapeutic gas independent of environmental pH for reliable CO generation at gastric, intestinal or colonic sites. In vivo experiments and toxicological assessments particularly with respect to observed ruthenium release of OCORS are required to demonstrate the pharmacokinetics and clinical potential of this oral delivery platform for therapeutic gases. PMID:24969354

  15. Enhanced adsorption of acidic gases (CO2, NO2 and SO2) on light metal decorated graphene oxide.

    PubMed

    Chen, Chi; Xu, Kui; Ji, Xiao; Miao, Ling; Jiang, Jianjun

    2014-06-14

    The adsorption of several acidic gases (CO2, NO2 and SO2) on light metal (Li, Al) decorated graphene oxide (GO) is theoretically studied, based on the first-principles calculations. Configuration relaxation, binding energy and charge transfer are carried out to discuss the acidic gas adsorption ability of light metal decorated GO. It is found out that Li, Al could be anchored stably by hydroxyl and epoxy groups on GO, and then a strong adsorption of CO2, NO2 and SO2 will occur above these light metals. In contrast to Ti, Li decorated GO exhibits a comparable adsorption ability of acidic gases, but a much smaller interaction with O2 about 2.85-3.98 eV lower in binding energy; and Al decorated GO displays much higher binding energy of all acidic gases with an enhancement of about 0.59-2.29 eV. The results of enhanced acidic gas adsorption ability and a reduced interference by O2 imply that Li, Al decorated GO may be useful and promising for collection and filtration of exhaust gases. PMID:24777197

  16. SEPARATION OF CO2 FROM FLUE GASES BY CARBON-MULTIWALL CARBON NANOTUBE MEMBRANES

    SciTech Connect

    Rodney Andrews

    2001-11-01

    Multiwalled carbon nanotubes (MWNT) were found to be an effective separation media for removing CO{sub 2} from N{sub 2}. The separation mechanism favors the selective condensation of CO{sub 2} from the flowing gas stream. Significant uptakes of CO{sub 2} were measured at 30 C, 150 C and 300 C over the pressure range 0.5 to 5 bar. No measurable uptake of nitrogen was found for this range of conditions. The mass uptake of CO{sub 2} by MWNT was found to increase with increasing temperature. A packed bed of MWNT completely removed CO{sub 2} from a flowing stream of CO{sub 2}/N{sub 2}, and exhibited rapid uptake kinetics for CO{sub 2}.

  17. SEPARATION OF CO2 FROM FLUE GASES BY CARBON-MULTIWALL CARBON NANOTUBE MEMBRANES

    SciTech Connect

    Rodney Andrews

    2001-03-01

    Multiwalled carbon nanotubes (MWNT) were found to be an effective separation media for removing CO{sub 2} from N{sub 2}. The separation mechanism favors the selective condensation of CO{sub 2} from the flowing gas stream. Significant uptakes of CO{sub 2} were measured at 30 C and 150 C over the pressure range 0.5 to 5 bar. No measurable uptake of nitrogen was found for this range of conditions. The mass uptake of CO{sub 2} by MWNT was found to increase with increasing temperature. A packed bed of MWNT completely removed CO{sub 2} from a flowing stream of CO{sub 2}/N{sub 2}, and exhibited rapid uptake kinetics for CO{sub 2}.

  18. Oceanic Trace Gases Numeric Data Packages from the Carbon Dioxide Information Analysis Center (CDIAC)

    DOE Data Explorer

    CDIAC products include numeric data packages, publications, trend data, atlases, models, etc. and can be searched for by subject area, keywords, authors, product numbers, time periods, collection sites, spatial references, etc. Most data sets or packages, many with numerous data files, are free to download from CDIAC's ftp area. CDIAC lists the following numeric data packages under the broad heading of Oceanic Trace Gases: Carbon Dioxide, Hydrographic, and Chemical Data Obtained during the R/V Ronald H. Brown Repeat Hydrography Cruise in the Atlantic Ocean: CLIVAR CO2 Section A16S_2005 ( 01/11/05 - 022405) Determination of Carbon Dioxide, Hydrographic, and Chemical Parameters during the R/V Nathaniel B. Palmer Cruise in the Southern Indian Ocean (WOCE Section S04I, 050396 - 070496) Inorganic Carbon, Nutrient, and Oxygen Data from the R/V Ronald H. Brown Repeat Hydrography Cruise in the Atlantic Ocean: CLIVAR CO2 Section A16N_2003a (060403 081103) Carbon Dioxide, Hydrographic, and Chemical Data Obtained During the R/V Maurice Ewing Cruise in the Atlantic Ocean (WOCE Section A17, 010494 - 032194) Global Ocean Data Analysis Project GLODAP: Results and Data Carbon Dioxide, Hydrographic, and Chemical Data Obtained During the R/V Knorr Cruises in the North Atlantic Ocean on WOCE Sections AR24 (1102 120596) and A24, A20, and A22 (053097 090397) Carbon Dioxide, Hydrographic and Chemical Data Obtained During the Nine R/V Knorr Cruises Comprising the Indian Ocean CO2 Survey (WOCE Sections I8SI9S, I9N, I8NI5E, I3, I5WI4, I7N, I1, I10, and I2; 120 194 012296) Carbon Dioxide, Hydrographic, and Chemical Data Obtained During the R/V Meteor Cruise 28/1 in the South Atlantic Ocean (WOCE Section A8, 032994 - 051294) Carbon Dioxide, Hydrographic, and Chemical Data Obtained During the R/V Knorr Cruise 138-3, -4, and -5 in the South Pacific Ocean (WOCE Sections P6E, P6C, and P6W, 050292 - 073092) Global Distribution of Total Inorganic Carbon and Total Alkalinity below the deepest winter mixed layer depths Carbon Dioxide, Hydrographic, and Chemical Data Obtained During the R/V John V. Vickers Cruise in the Pacific Ocean (WOCE Section P13, NOAA CGC92 Cruise, 080492 102192) Carbon Dioxide, Hydrographic, and Chemical Data Obtained During the R/V Hesperides Cruise in the Atlantic Ocean (WOCE Section A5, 071492 - 081592) Carbon Dioxide, Hydrographic, and Chemical Data Obtained During the R/V Thomas G. Thompson Cruise in the Pacific Ocean (WOCE Section P10, 100593 111093) The International Intercomparison Exercise of Underway fCO2 Systems during the R/V Meteor Cruise 36/1 in the North Atlantic Ocean Carbon Dioxide, Hydrographic, and Chemical Data Obtained during the R/V Meteor Cruise 22/5 in the South Atlantic Ocean (WOCE Section A10, Dec. 1992-Jan, 1993) Carbon Dioxide, Hydrographic, and Chemical Data Obtained in the South Pacific Ocean (WOCE Sections P16A/P17A, P17E/P19S, and P19C, R/V Knorr , Oct. 1992-April 1993) Surface Water and Atmospheric Underway Carbon Data Obtained During the World Ocean Circulation Experiment Indian Ocean Survey Cruises (R/V Knorr, Dec. 1994 Jan, 1996) Carbon Dioxide, Hydrographic, and Chemical Data Obtained During the R/V Akademik Ioffe Cruise in the South Pacific Ocean (WOCE Section S4P, Feb.-April 1992) Carbon Dioxide, Hydrographic, and Chemical Data Obtained During the R/V Thomas Washington Cruise TUNES-1 in the Equatorial Pacific Ocean (WOCE section P17C) Carbon Dioxide, Hydrographic, and Chemical Data Obtained During the R/V Thomas Washington Cruise TUNES-3 in the Equatorial Pacific Ocean (WOCE section P16C) Carbon-14 Measurements in Surface Water CO2 from the Atlantic, Indian and Pacific Oceans, 1965-1994 Carbon Dioxide, Hydrographic, and Chemical Data Obtained During R/V Meteor Cruise 18/1 in the North Atlantic Ocean (WOCE Section A1E) Carbon Dioxide, Hydrographic, and Chemical Data Obtained in the Central South Pacific Ocean (WOCE Sections P17S and P16S) during the TUNES-2 Expedition of the R/V Th

  19. Biological production of products from waste gases

    DOEpatents

    Gaddy, James L.

    2002-01-22

    A method and apparatus are designed for converting waste gases from industrial processes such as oil refining, and carbon black, coke, ammonia, and methanol production, into useful products. The method includes introducing the waste gases into a bioreactor where they are fermented to various products, such as organic acids, alcohols, hydrogen, single cell protein, and salts of organic acids by anaerobic bacteria within the bioreactor. These valuable end products are then recovered, separated and purified.

  20. Understanding the contribution of non-carbon dioxide gases in deep mitigation scenarios

    SciTech Connect

    Gernaat, David; Calvin, Katherine V.; Lucas, Paul; Luderer, Gunnar; Otto, Sander; Rao, Shilpa; Strefler, Jessica; Van Vuuren, Detlef

    2015-07-01

    The combined 2010 emissions of methane (CH4), nitrous oxide (N2O) and the fluorinated gasses (F-gas) account for about 20-30% of total emissions and about 30% of radiative forcing. At the moment, most studies looking at reaching ambitious climate targets project the emission of carbon dioxide (CO2) to be reduced to zero (or less) by the end of the century. As for non-CO2 gases, the mitigation potential seem to be more constrained, we find that by the end of the century in the current deep mitigation scenarios non-CO2 emissions could form the lion’s share of remaining greenhouse gas emissions. In order to support effective climate policy strategies, in this paper we provide a more in-depth look at the role of non-CO2¬ emission sources (CH4, N2O and F-gases) in achieving deep mitigation targets (radiative forcing target of 2.8 W/m2 in 2100). Specifically, we look at the sectorial mitigation potential and the remaining non-CO2 emissions. By including a set of different models, we provide some insights into the associated uncertainty. Most of the remaining methane emissions in 2100 in the climate mitigation scenario come from the livestock sector. Strong reductions are seen in the energy supply sector across all models. For N2O, less reduction potential is seen compared to methane and the sectoral differences are larger between the models. The paper shows that the assumptions on remaining non-CO2 emissions are critical for the feasibility of reaching ambitious climate targets and the associated costs.

  1. 40 CFR 60.52b - Standards for municipal waste combustor metals, acid gases, organics, and nitrogen oxides.

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ... 40 Protection of Environment 7 2014-07-01 2014-07-01 false Standards for municipal waste combustor... SOURCES Standards of Performance for Large Municipal Waste Combustors for Which Construction is Commenced... 60.52b Standards for municipal waste combustor metals, acid gases, organics, and nitrogen oxides....

  2. 40 CFR 60.52b - Standards for municipal waste combustor metals, acid gases, organics, and nitrogen oxides.

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ... 40 Protection of Environment 7 2013-07-01 2013-07-01 false Standards for municipal waste combustor... SOURCES Standards of Performance for Large Municipal Waste Combustors for Which Construction is Commenced... 60.52b Standards for municipal waste combustor metals, acid gases, organics, and nitrogen oxides....

  3. High temperature abatement of acid gases from waste incineration. Part II: Comparative life cycle assessment study

    SciTech Connect

    Biganzoli, Laura; Racanella, Gaia; Marras, Roberto; Rigamonti, Lucia

    2015-01-15

    Highlights: • Two scenarios of acid gases removal in WTE plants were compared in an LCA study. • A detailed inventory based on primary data has been reported for the production of the new dolomitic sorbent. • Results show that the comparison between the two scenarios does not show systematic differences. • The potential impacts are reduced only if there is an increase in the energy efficiency of the WTE plant. - Abstract: The performances of a new dolomitic sorbent, named Depurcal®MG, to be directly injected at high temperature in the combustion chamber of Waste-To-Energy (WTE) plants as a preliminary stage of deacidification, were experimentally tested during full-scale commercial operation. Results of the experimentations were promising, and have been extensively described in Biganzoli et al. (2014). This paper reports the Life Cycle Assessment (LCA) study performed to compare the traditional operation of the plants, based on the sole sodium bicarbonate feeding at low temperature, with the new one, where the dolomitic sorbent is injected at high temperature. In the latter the sodium bicarbonate is still used, but at lower rate because of the decreased load of acid gases entering the flue gas treatment line. The major goal of the LCA was to make sure that a burden shifting was not taking place somewhere in the life cycle stages, as it might be the case when a new material is used in substitution of another one. According to the comparative approach, only the processes which differ between the two operational modes were included in the system boundaries. They are the production of the two reactants and the treatment of the corresponding solid residues arising from the neutralisation of acid gases. The additional CO{sub 2} emission at the stack of the WTE plant due to the activation of the sodium bicarbonate was also included in the calculation. Data used in the modelling of the foreground system are primary, derived from the experimental tests described in Biganzoli et al. (2014) and from the dolomitic sorbent production plant. The results of the LCA show minor changes in the potential impacts between the two operational modes of the plants. These differences are for 8 impact categories in favour of the new operational mode based on the addition of the dolomitic sorbent, and for 7 impact categories in favour of the traditional operation. A final evaluation was conducted on the potential role of the dolomitic sorbent in enhancing the electric energy production efficiency of the plant, thanks to the better cleaning of the heat exchange surface that can be achieved. If such improvement is accounted for, all the potential impacts are considerably decreased (e.g. the Climate change by 28%), and in the comparison with the traditional operation 17 impact categories out of 19 are reduced.

  4. High temperature abatement of acid gases from waste incineration. Part II: Comparative life cycle assessment study.

    PubMed

    Biganzoli, Laura; Racanella, Gaia; Marras, Roberto; Rigamonti, Lucia

    2015-01-01

    The performances of a new dolomitic sorbent, named DepurcalMG, to be directly injected at high temperature in the combustion chamber of Waste-To-Energy (WTE) plants as a preliminary stage of deacidification, were experimentally tested during full-scale commercial operation. Results of the experimentations were promising, and have been extensively described in Biganzoli et al. (2014). This paper reports the Life Cycle Assessment (LCA) study performed to compare the traditional operation of the plants, based on the sole sodium bicarbonate feeding at low temperature, with the new one, where the dolomitic sorbent is injected at high temperature. In the latter the sodium bicarbonate is still used, but at lower rate because of the decreased load of acid gases entering the flue gas treatment line. The major goal of the LCA was to make sure that a burden shifting was not taking place somewhere in the life cycle stages, as it might be the case when a new material is used in substitution of another one. According to the comparative approach, only the processes which differ between the two operational modes were included in the system boundaries. They are the production of the two reactants and the treatment of the corresponding solid residues arising from the neutralisation of acid gases. The additional CO2 emission at the stack of the WTE plant due to the activation of the sodium bicarbonate was also included in the calculation. Data used in the modelling of the foreground system are primary, derived from the experimental tests described in Biganzoli et al. (2014) and from the dolomitic sorbent production plant. The results of the LCA show minor changes in the potential impacts between the two operational modes of the plants. These differences are for 8 impact categories in favour of the new operational mode based on the addition of the dolomitic sorbent, and for 7 impact categories in favour of the traditional operation. A final evaluation was conducted on the potential role of the dolomitic sorbent in enhancing the electric energy production efficiency of the plant, thanks to the better cleaning of the heat exchange surface that can be achieved. If such improvement is accounted for, all the potential impacts are considerably decreased (e.g. the Climate change by 28%), and in the comparison with the traditional operation 17 impact categories out of 19 are reduced. PMID:25465510

  5. Colloidally separated samples from Allende residues - Noble gases, carbon and an ESCA-study

    NASA Technical Reports Server (NTRS)

    Ott, U.; Kronenbitter, J.; Flores, J.; Chang, S.

    1984-01-01

    Results are presented which strengthen the hypothesis of heterogeneity among the carbon- and nitrogen-bearing phases of the Allende meteorite. These data also highlight the possibility of performing physical separations yielding samples in which some of the noble gas- and carbon-bearing phases are extraordinarily predominant over others. The conclusion, based on mass and isotope balance arguments, that a significant portion of the carbonaceous matter in Allende is likely to be gas-poor or gas-free need not weaken the case for carbonaceous carriers for the major noble gas components. The concept that acid-soluble carbonaceous phases contain a multiplicity of components, each of which may have formed under a multiplicity of different physical-chemical conditions, is reemphasized by the results of the present study.

  6. Equivalent Circuit Modeling for Carbon Nanotube Schottky Barrier Modulation in Polarized Gases

    NASA Technical Reports Server (NTRS)

    Yamada, Toshishige

    2005-01-01

    We study the carbon nanotube Schottky barrier at the metallic electrode interface in polarized gases using an equivalent circuit model. The gas-nanotube interaction is often weak and very little charge transfer is expected [l]. This is the case with'oxygen, but the gas-electrode interaction is appreciable and makes the oxygen molecules negatively charged. In the closed circuit condition, screening positive charges appear in the nanotube as well as in the electrode, and the Schottky barrier is modulated due to the resultant electrostatic effects [2]. In the case of ammonia, both the gas-nanotube and gas-electrode interactions are weak, but the Schottky barrier can still be modulated since the molecules are polarized and align in the preferred orientation within the gap between the electrode and nanotube in the open circuit condition (dipole layer formation). In the closed circuit condition, an electric field appears in the gap and strengthens or weakens the preferred dipole alignment reflecting the nanotube Fermi level. The modulation is visible when the nanotube depletion mode is involved, and the required dipole density is as low as 2 x 10(exp 13) dipoles/sq cm, which is quite feasible experimentally,

  7. Interstellar Diamond: The Analysis Results for Carbon, Nitrogen, and Noble Gases in Different Grain-Size Fractions

    NASA Astrophysics Data System (ADS)

    Fisenko, A. V.; Verhovsky, A. B.; Semjonova, L. F.; Pillinger, C. T.

    The content and isotopic composition of carbon, nitrogen, and noble gases in different grain-size fractions of interstellar diamond from the Efremovka chondrite have been established for the first time. Using these data as the base, we have found the following. (a) All isotopically anomalous components of C, N, and noble gases and the characteristic features of the release of these components, revealed for bulk samples of dia- mond, are also inherent in diamond fractions. At the same time, the fractions differ drastically in the proportion of the isotopically anomalous and normal components and in the elemental ratios of noble gases. (b) Mixing of two components for carbon, as well as for nitrogen (one of these components is in the surface layer of diamond and enriched with 13C and 15N), results in the observed variations of isotopic composition of these elements released in the stepped combustion of diamond fractions. (c) The nitrogen-content variations during diamond- grain oxidation are most probably determined by the diffusion loss of nitrogen, which occurred mainly before the integration of diamond with the material of the chondrite-parent bodies (for example, at the period of dia- mond formation or in the second heating). (d) The combination of the process of implantation of noble gases into diamond grains in at least two events, with the following diffusion loss, led to the heterogeneous distribu- tion of noble gases in the grain volume. The revealed peculiarities of distribution and isotopic content of C, N, and noble gases in the fractions of interstellar diamond have been invoked for establishing the main stages of its formation during an extremely nonequilibrium process.

  8. Annular denuders for use in global climate and stratospheric measurements of acidic gases and particles

    NASA Astrophysics Data System (ADS)

    Stevens, Robert K.

    1991-02-01

    Measurements of acidic and basic gases that coexist with fine particle (less than 2.5 micron) may be useful for determining the impact of these species on global climate changes and determining species that influence stratospheric ozone levels. Annular denuders are well suited for this purpose. A new concentric annular denuder system, consisting of a three channel denuder, a Teflon coated cyclone preseparator, and a multistage filter pack was developed, evaluated, and shown to provide reliable atmospheric measurements of SO2, HNO2, HNO3, NH3, SO4(=), NH4(+), NO3(-), and H(+). For example, the precision of the annular denuder for the ambient measurements of HNO3 and nitrates at concentrations between 0.1 to 3 microgram/cu m was + or - 12 and 16 pct., respectively. The 120 x 25 mm three channel denuder is encased in a stainless steel sheath and has annular spaces that are 1 mm wide. This design was shown to have nearly identical capacity for removal of SO2 as conventional 210 x 25 mm single channel denuder configurations. The cyclone preseparator was designed and tested to have a D sub 50 cutoff diameter of 2.5 micron and minimal retention of HNO3.

  9. Annular denuders for use in global climate and stratospheric measurements of acidic gases and particles

    NASA Technical Reports Server (NTRS)

    Stevens, Robert K.

    1991-01-01

    Measurements of acidic and basic gases that coexist with fine particle (less than 2.5 micron) may be useful for determining the impact of these species on global climate changes and determining species that influence stratospheric ozone levels. Annular denuders are well suited for this purpose. A new concentric annular denuder system, consisting of a three channel denuder, a Teflon coated cyclone preseparator, and a multistage filter pack was developed, evaluated, and shown to provide reliable atmospheric measurements of SO2, HNO2, HNO3, NH3, SO4(=), NH4(+), NO3(-), and H(+). For example, the precision of the annular denuder for the ambient measurements of HNO3 and nitrates at concentrations between 0.1 to 3 microgram/cu m was + or - 12 and 16 pct., respectively. The 120 x 25 mm three channel denuder is encased in a stainless steel sheath and has annular spaces that are 1 mm wide. This design was shown to have nearly identical capacity for removal of SO2 as conventional 210 x 25 mm single channel denuder configurations. The cyclone preseparator was designed and tested to have a D sub 50 cutoff diameter of 2.5 micron and minimal retention of HNO3.

  10. Sources of greenhouse gases and carbon monoxide in central London (UK)

    NASA Astrophysics Data System (ADS)

    Helfter, Carole; Tremper, Anja; Zazzeri, Giulia; Barlow, Janet F.; Nemitz, Eiko

    2015-04-01

    Biosphere-atmosphere exchange of carbon dioxide (CO2) has been on the scientific agenda for several decades and new technology now also allows for high-precision, continuous monitoring of fluxes of methane (CH4) and nitrous oxide (N2O). Compared to the natural environment, flux measurements in the urban environment, which is home to over 50% of the population globally, are still rare despite high densities of anthropogenic sources of pollutants. We report on over three years of measurements atop a 192 m tower in central London (UK), Europe's largest city, which started in October 2011. Fluxes of methane, carbon monoxide (CO) and carbon dioxide are measured by eddy-covariance (EC) at the British Telecom tower (51° 31' 17.4' N 0° 8' 20.04' W). In addition to the long-term measurements, EC fluxes of nitrous oxide (N2O) were measured in February 2014. All four trace gases exhibit diurnal trends consistent with anthropogenic activities with minimum emissions at night and early afternoon maxima. Segregating emissions by wind direction reveals heterogeneous source distributions with temporal patterns and source strengths that differ between compounds. The lowest emissions for CO, CO2 and CH4 were recorded for NW winds. The highest emissions of methane were in the SE sector, in the NE for CO2 and in the W for CO. Fluxes of all 3 gases exhibited marked seasonal trends characterised by a decrease in emissions in summer (63% reduction for CO, 36% for CO2 and 22% for CH4). Monthly fluxes of CO and CO2 were linearly correlated to air temperature (R2 = 0.7 and 0.59 respectively); a weaker dependence upon temperature was also observed for CH4 (R2 = 0.31). Diurnal and seasonal emissions of CO and CO2 are mainly controlled by local fossil fuel combustion and vehicle cold starts are thought to account for 20-30% of additional emissions of CO during the winter. Fugitive emissions of CH4 from the natural gas distribution network are thought to be substantial, which is consistent with the weaker seasonality of CH4 fluxes compared with CO and CO2. Annual estimates of CO2 emissions (41 kt km-2) obtained by EC were consistent with data upscaled from the London Atmospheric Emissions Inventory (LAEI; 46 kt km-2). Good agreement between measurements and inventory data was also found for CO (measured 156 t km-2; LAEI 145 t km-2) and for N2O (measured 0.36 t km-2; LAEI 0.42 t km-2), although based on a much shorter measurement period. By contrast, a two-fold difference was found between inventory and measured CH4 fluxes (measured 75 t km-2; LAEI 34 t km-2), which could indicate an underestimation by the inventory of CH4 emissions from anthropogenic sources or the existence of unaccounted biogenic sources. Measurements of isotopic CH4 taken 2 km SE of the tower near the banks of the river Thames reveal multiple episodes of 13C-depleted morning peaks consistent with biogenic sources. We speculate that the Thames can act as an additional significant source of biogenic methane especially at low tide and after heavy rainfall, which could explain the large emissions observed in the S-SE sector.

  11. Carbon Dioxide Information Analysis Center and World Data Center for Atmospheric Trace Gases Fiscal Year 2000 Annual Report

    SciTech Connect

    Cushman, R.M.

    2001-11-15

    The Carbon Dioxide Information Analysis Center (CDIAC), which includes the World Data Center (WDC) for Atmospheric Trace Gases, is the primary global change data and information analysis center of the U.S. Department of Energy (DOE). More than just an archive of data sets and publications, CDIAC has, since its inception in 1982, enhanced the value of its holdings through intensive quality assurance, documentation, and integration. Whereas many traditional data centers are discipline-based (for example, meteorology or oceanography), CDIAC's scope includes potentially anything and everything that would be of value to users concerned with the greenhouse effect and global climate change, including concentrations of carbon dioxide (CO{sub 2}) and other radiatively active gases in the atmosphere; the role of the terrestrial biosphere and the oceans in the biogeochemical cycles of greenhouse gases; emissions of CO{sub 2} and other trace gases to the atmosphere; long-term climate trends; the effects of elevated CO{sub 2} on vegetation; and the vulnerability of coastal areas to rising sea levels.

  12. The southern Brazilian grassland biome: soil carbon stocks, fluxes of greenhouse gases and some options for mitigation.

    PubMed

    Pillar, V D; Tornquist, C G; Bayer, C

    2012-08-01

    The southern Brazilian grassland biome contains highly diverse natural ecosystems that have been used for centuries for grazing livestock and that also provide other important environmental services. Here we outline the main factors controlling ecosystem processes, review and discuss the available data on soil carbon stocks and greenhouse gases emissions from soils, and suggest opportunities for mitigation of climatic change. The research on carbon and greenhouse gases emissions in these ecosystems is recent and the results are still fragmented. The available data indicate that the southern Brazilian natural grassland ecosystems under adequate management contain important stocks of organic carbon in the soil, and therefore their conservation is relevant for the mitigation of climate change. Furthermore, these ecosystems show a great and rapid loss of soil organic carbon when converted to crops based on conventional tillage practices. However, in the already converted areas there is potential to mitigate greenhouse gas emissions by using cropping systems based on no soil tillage and cover-crops, and the effect is mainly related to the potential of these crop systems to accumulate soil organic carbon in the soil at rates that surpass the increased soil nitrous oxide emissions. Further modelling with these results associated with geographic information systems could generate regional estimates of carbon balance. PMID:23011297

  13. Hydroquinone and Quinone-Grafted Porous Carbons for Highly Selective CO2 Capture from Flue Gases and Natural Gas Upgrading.

    PubMed

    Wang, Jun; Krishna, Rajamani; Yang, Jiangfeng; Deng, Shuguang

    2015-08-01

    Hydroquinone and quinone functional groups were grafted onto a hierarchical porous carbon framework via the Friedel-Crafts reaction to develop more efficient adsorbents for the selective capture and removal of carbon dioxide from flue gases and natural gas. The oxygen-doped porous carbons were characterized with scanning electron microscopy, transmission electron microscopy, X-ray powder diffraction, Fourier transform infrared spectroscopy, and Raman spectroscopy. CO2, CH4, and N2 adsorption isotherms were measured and correlated with the Langmuir model. An ideal adsorbed solution theory (IAST) selectivity for the CO2/N2 separation of 26.5 (298 K, 1 atm) was obtained on the hydroquinone-grafted carbon, which is 58.7% higher than that of the pristine porous carbon, and a CO2/CH4 selectivity value of 4.6 (298 K, 1 atm) was obtained on the quinone-grafted carbon (OAC-2), which represents a 28.4% improvement over the pristine porous carbon. The highest CO2 adsorption capacity on the oxygen-doped carbon adsorbents is 3.46 mmol g(-1) at 298 K and 1 atm. In addition, transient breakthrough simulations for CO2/CH4/N2 mixture separation were conducted to demonstrate the good separation performance of the oxygen-doped carbons in fixed bed adsorbers. Combining excellent adsorption separation properties and low heats of adsorption, the oxygen-doped carbons developed in this work appear to be very promising for flue gas treatment and natural gas upgrading. PMID:26114815

  14. STABILITY EVALUATION OF SULFUR DIOXIDE, NITRIC OXIDE AND CARBON MONOXIDE GASES IN CYLINDERS

    EPA Science Inventory

    The US EPA recommends in their EPA Traceability Protocol 1 and 2 that reactive gases be reanalyzed every six months. The purpose of this study was to assess the stability of selected reactive gases as a function of time to determine the feasibility of extending the recertificatio...

  15. Impact of oxy-fuel combustion gases on mercury retention in activated carbons from a macroalgae waste: effect of water.

    PubMed

    Lopez-Anton, M A; Ferrera-Lorenzo, N; Fuente, E; Díaz-Somoano, M; Suarez-Ruíz, I; Martínez-Tarazona, M R; Ruiz, B

    2015-04-01

    The aim of this study is to understand the different sorption behaviors of mercury species on activated carbons in the oxy-fuel combustion of coal and the effect of high quantities of water vapor on the retention process. The work evaluates the interactions between the mercury species and a series of activated carbons prepared from a macroalgae waste (algae meal) from the agar-agar industry in oxy-combustion atmospheres, focussing on the role that the high concentration of water in the flue gases plays in mercury retention. Two novel aspects are considered in this work (i) the impact of oxy-combustion gases on the retention of mercury by activated carbons and (ii) the performance of activated carbons prepared from biomass algae wastes for this application. The results obtained at laboratory scale indicate that the effect of the chemical and textural characteristics of the activated carbons on mercury capture is not as important as that of reactive gases, such as the SOx and water vapor present in the flue gas. Mercury retention was found to be much lower in the oxy-combustion atmosphere than in the O2+N2 (12.6% O2) atmosphere. However, the oxidation of elemental mercury (Hg0) to form oxidized mercury (Hg2+) amounted to 60%, resulting in an enhancement of mercury retention in the flue gas desulfurization units and a reduction in the amalgamation of Hg0 in the CO2 compression unit. This result is of considerable importance for the development of technologies based on activated carbon sorbents for mercury control in oxy-combustion processes. PMID:25585865

  16. Advanced fire-resistant forms of activated carbon and methods of adsorbing and separating gases using same

    SciTech Connect

    Xiong, Yongliang; Wang, Yifeng

    2015-02-03

    Advanced, fire-resistant activated carbon compositions useful in adsorbing gases; and having vastly improved fire resistance are provided, and methods for synthesizing the compositions are also provided. The advanced compositions have high gas adsorption capacities and rapid adsorption kinetics (comparable to commercially-available activated carbon), without having any intrinsic fire hazard. They also have superior performance to Mordenites in both adsorption capacities and kinetics. In addition, the advanced compositions do not pose the fibrous inhalation hazard that exists with use of Mordenites. The fire-resistant compositions combine activated carbon mixed with one or more hydrated and/or carbonate-containing minerals that release H.sub.2O and/or CO.sub.2 when heated. This effect raises the spontaneous ignition temperature to over 500.degree. C. in most examples, and over 800.degree. C. in some examples. Also provided are methods for removing and/or separating target gases, such as Krypton or Argon, from a gas stream by using such advanced activated carbons.

  17. Low to middle tropospheric profiles and biosphere/troposphere fluxes of acidic gases in the summertime Canadian taiga

    NASA Technical Reports Server (NTRS)

    Klemm, O.; Talbot, R. W.; Fitzgerald, D. R.; Klemm, K. I.; Lefer, B. L.

    1994-01-01

    We report features of acidic gases in the troposphere from 9 to 5000 m altitude above ground over the Canadian taiga in the summer of 1990. The measurements were conducted at a 30-m meteorological tower and from the NASA Wallops Electra aircraft as part of the joint U.S.-Canadian Arctic Boundary Layer Expedition (ABLE) 3B Northern Wetland Studies (NOWES). We sampled air for acidic gases using the mist chamber collector coupled with subsequent analysis using ion chromatography. At the tower we collected samples at two heights during a 13-day period, including diurnal studies. Using eddy flux and profile data, we estimated the biosphere/troposphere fluxes of nitric, formic, and acetic acids and sulfur dioxide. For the organic acids, emissions from the taiga in the afternoon hours and deposition during the predawn morning hours were observed. The flux intensities alone were however not high enough to explain the observed changes in mixing ratios. The measured deposition fluxes of nitric acid were high enough to have a significant influence on its mixing ratio in the boundary layer. On three days we measured vertical profiles of nitric, formic, and acetic acids through the lower to midtroposphere. We found that the chemical composition of the troposphere was extremely heterogenous. Pronounced layers of polluted air were readily apparent from our measurements. Local photochemical production and episodic long-range transport of trace components, originating from biomass burning and possibly industrial emissions, appear to have a strong influence on the composition of the troposphere and biosphere/troposphere fluxes of acidic gases at this site.

  18. Detection of a CO and NH3 gas mixture using carboxylic acid-functionalized single-walled carbon nanotubes.

    PubMed

    Dong, Ki-Young; Choi, Jinnil; Lee, Yang Doo; Kang, Byung Hyun; Yu, Youn-Yeol; Choi, Hyang Hee; Ju, Byeong-Kwon

    2013-01-01

    Carbon nanotubes (CNT) are extremely sensitive to environmental gases. However, detection of mixture gas is still a challenge. Here, we report that 10 ppm of carbon monoxide (CO) and ammonia (NH3) can be electrically detected using a carboxylic acid-functionalized single-walled carbon nanotubes (C-SWCNT). CO and NH3 gases were mixed carefully with the same concentrations of 10 ppm. Our sensor showed faster response to the CO gas than the NH3 gas. The sensing properties and effect of carboxylic acid group were demonstrated, and C-SWCNT sensors with good repeatability and fast responses over a range of concentrations may be used as a simple and effective detection method of CO and NH3 mixture gas. PMID:23286690

  19. Detection of a CO and NH3 gas mixture using carboxylic acid-functionalized single-walled carbon nanotubes

    PubMed Central

    2013-01-01

    Carbon nanotubes (CNT) are extremely sensitive to environmental gases. However, detection of mixture gas is still a challenge. Here, we report that 10 ppm of carbon monoxide (CO) and ammonia (NH3) can be electrically detected using a carboxylic acid-functionalized single-walled carbon nanotubes (C-SWCNT). CO and NH3 gases were mixed carefully with the same concentrations of 10 ppm. Our sensor showed faster response to the CO gas than the NH3 gas. The sensing properties and effect of carboxylic acid group were demonstrated, and C-SWCNT sensors with good repeatability and fast responses over a range of concentrations may be used as a simple and effective detection method of CO and NH3 mixture gas. PMID:23286690

  20. Isotope composition of carbon in amino acids of solid bitumens

    NASA Astrophysics Data System (ADS)

    Shanina, S. N.; Bushnev, D. A.

    2014-06-01

    Primary data are presented on the isotope composition of carbon in individual amino acids from solid bitumens and several biological objects. The amino acids of biological objects are characterized by wide variations of the isotope composition of carbon. This fact occurs owing to the difference in biochemical paths of metabolism resulting in the synthesis of individual amino acids. The ?13C values are somewhat decreased for individual amino acids in asphaltenes, varying from -7.7 to -31.7. The carbon of amino acids is weighted in kerits from Bad'el' compared to asphaltenes. All the natural bitumens retain the characteristic trend for natural substances: the isotopically heavy and light amino acids by carbon are glycine and leucine, respectively. The isotope composition of amino-acid carbon is lightened compared to natural bitumens in the samples formed under a pronounced thermal impact (asphalt-like crust and kirishite).

  1. The air we breathe: three vital respiratory gases and the red blood cell: oxygen, nitric oxide, and carbon dioxide.

    PubMed

    Dzik, Walter H

    2011-04-01

    Three vital respiratory gases-oxygen (O(2)), nitric oxide (NO), and carbon dioxide (CO(2))-intersect at the level of the human red blood cell (RBC). In addition to hemoglobin (Hb)'s central role in O(2) transport, interaction of Hb with the Band 3 metabolon balances RBC energy flow. 2,3-Diphosphoglycerate enhances O(2) transport across the placenta and plays an important role in regulating RBC plasticity. NO is a key mediator of hypoxic vasodilation, but the precise role of RBC Hb remains controversial. In addition to established theories that depend on RBC uptake, delivery, and discharge of NO or its metabolites, an alternative hypothesis based on RBC permeability is suggested. NO depletion by free Hb may account for several clinical features seen during intravascular hemolysis or during deliberate infusion of Hb solutions used as RBC substitutes. CO(2) released by tissues triggers oxygen release through a series of well-coordinated reactions centered on the Band 3 metabolon. While RBC carbonic anhydrase and the Band 3 anion exchanger are central to this process, there is surprisingly little research on the kinetics of CO(2) clearance by transfusion. The three RBC gases are directly related to the three principal gases of Earth's atmosphere. Human fossil fuel consumption dumps 90 million metric tons of carbon into the atmosphere annually. Increasing CO(2) levels are linked to global warming, melting Arctic ice, rising sea levels, and climate instability. Just as individual cells depend on balance of the three vital gases, so too will their balance determine survival of life on Earth. PMID:21496039

  2. High temperature abatement of acid gases from waste incineration. Part I: experimental tests in full scale plants.

    PubMed

    Biganzoli, Laura; Racanella, Gaia; Rigamonti, Lucia; Marras, Roberto; Grosso, Mario

    2015-02-01

    In recent years, several waste-to-energy plants in Italy have experienced an increase of the concentration of acid gases (HCl, SO2 and HF) in the raw gas. This is likely an indirect effect of the progressive decrease of the amount of treated municipal waste, which is partially replaced by commercial waste. The latter is characterised by a higher variability of its chemical composition because of the different origins, with possible increase of the load of halogen elements such as chlorine (Cl) and fluorine (F), as well as of sulphur (S). A new dolomitic sorbent was then tested in four waste-to-energy plants during standard operation as a pre-cleaning stage, to be directly injected at high temperature in the combustion chamber. For a sorbent injection of about 6 kg per tonne of waste, the decrease of acid gases concentration downstream the boiler was in the range of 7-37% (mean 23%) for HCl, 34-95% (mean 71%) for SO2 and 39-80% (mean 63%) for HF. This pre-abatement of acid gases allowed to decrease the feeding rate of the traditional low temperature sorbent (sodium bicarbonate in all four plants) by about 30%. Furthermore, it was observed by the plant operators that the sorbent helps to keep the boiler surfaces cleaner, with a possible reduction of the fouling phenomena and a consequent increase of the specific energy production. A preliminary quantitative estimate was carried out in one of the four plants. PMID:25465511

  3. Abnormal carbon and hydrogen isotopes of alkane gases from the Qingshen gas field, Songliao Basin, China, suggesting abiogenic alkanes?

    NASA Astrophysics Data System (ADS)

    Liu, Quanyou; Dai, Jinxing; Jin, Zhijun; Li, Jian; Wu, Xiaoqi; Meng, Qingqiang; Yang, Chun; Zhou, Qinghua; Feng, Zihui; Zhu, Dongya

    2016-01-01

    It is great debate that the alkane gases of abiogenic origin would constitute a major portion of the commercial accumulation of the Qingshen gas field, Songliao Basin, China. In this study, abiogenic gases characterized by heavy δ13C1 values, reversal of the usual carbon isotopic trend of C1-C5 alkanes, very narrow variation in δ2HC1 values, and low CH4/3He ratios associated with high R/Ra values (>1) were identified. The hydrocarbon gas in the Qingshen gas field is a mixture of thermogenic alkanes derived from Cretaceous mudstone (type I kerogen) or Jurassic coal (type III kerogen) and abiogenic alkanes (mainly CH4) from mantle degassing. A quantitative estimation of abiogenic alkanes contribution to the Qingshen gas field is made based on a δ13C1 vs. δ13C2 plot: about 30-40% of alkane gases in the Qingshen gas field, along with its helium, are estimated to be derived from the mantle via magmatic activity. Particularly, the abiogenic formation of CH4 generated from the reduction of CO2 by hydrothermal activity may contribute. Our study suggests that abiogenic alkane gases in certain geological settings could be more widespread than previously thought, and may accumulate into economic reservoirs.

  4. Making Carbon Emissions Remotely Sensible: Flux Observations of Carbon from an Airborne Laboratory (FOCAL), its Near-Surface Survey of Carbon Gases and Isotopologues on Alaska's North Slope

    NASA Astrophysics Data System (ADS)

    Dobosy, R.; Dumas, E. J.; Sayres, D. S.; Healy, C. E.; Munster, J. B.; Baker, B.; Anderson, J. G.

    2014-12-01

    Detailed process-oriented study of the mechanisms of conversion in the Arctic of fossil carbon to atmospheric gas is progressing, but necessarily limited to a few point locations and requiring detailed subsurface measurements inaccessible to remote sensing. Airborne measurements of concentration, transport and flux of these carbon gases at sufficiently low altitude to reflect surface variations can tie such local measurements to remotely observable features of the landscape. Carbon dioxide and water vapor have been observable for over 20 years from low-altitude small aircraft in the Arctic and elsewhere. Methane has been more difficult, requiring large powerful aircraft or limited flask samples. Recent developments in spectroscopy, however, have reduced the power and weight required to measure methane at rates suitable for eddy-covariance flux estimates. The Flux Observations of Carbon from an Airborne Laboratory (FOCAL) takes advantage of Integrated Cavity-Output Spectroscopy (ICOS) to measure CH4, CO2, and water vapor in a new airborne system. The system, moreover, measures these gases' stable isotopologues every two seconds or faster helping to separate thermogenic from biogenic emissions. Paired with the Best Airborne Turbulence (BAT) probe developed for small aircraft by NOAA's Air Resources Laboratory and a light twin-engine aircraft adapted by Aurora Flight Sciences Inc., the FOCAL measures at 6 m spacing, covering 100 km in less than 30 minutes. It flies between 10 m and 50 m above ground interspersed with profiles to the top of the boundary layer and beyond. This presentation gives an overview of the magnitude and variation in fluxes and concentrations of CH4, CO2, and H2O with space, time, and time of day in a spatially extensive survey, more than 7500 km total in 15 flights over roughly a 100 km square during the month of August 2013. An extensive data set such as this at low altitude with high-rate sampling addresses features that repeat on 1 km scale or smaller such as thermokarst lakes as well as landscape changes on the 100 km scale.

  5. Adsorption and dissociation of acidic trace gases on ice surfaces - caught in the act with core level spectroscopy

    NASA Astrophysics Data System (ADS)

    Waldner, Astrid; Orlando, Fabrizio; Ammann, Markus; Kleibert, Armin; Huthwelker, Thomas; Peter, Thomas; Bartels-Rausch, Thorsten

    2015-04-01

    Chemistry and physical processes in Earth's ice and snow cover can change the composition of the atmosphere and the contaminant content of the cryosphere. They have thus direct impacts on geochemical cycles and the climate system. Our ability to predict the fate of chemicals in snow or air masses in exchange with the cryosphere on a regional scale or to model those in snow chemistry models is currently hampered by our limited understanding of the underlying mechanisms on a molecular level. So far, direct experimental observations under environmentally relevant conditions of the ice surface and of the adsorption of trace gases to it are very limited. The unique approach of this study is to combine two surface sensitive spectroscopic methods to directly probe the hydrogen-bonding network at the ice surface ( ~1 nm depth) and the concentration, depth profile (~1 to 10 nm), and dissociation degree of the dopant. We present first core-electron photoemission (XPS) and partial electron yield X-ray absorption (NEXAFS) measurements of formic acid adsorbed to ice at 240 K. The analysis of oxygen NEXAFS spectra reveals information on changes in the hydrogen-bonding network of the ice surface upon adsorption of formic acid. Depth profiles based on XPS measurements indicate that the adsorbed acid stays at the ice surface. Furthermore we obtained a preliminary estimation of the degree of formic acid dissociation at the ice surface. Results are compared to earlier core-electron studies of several trace gases adsorbed to ice at 240 K and compared to results from more traditional method to and snow to reveal fundamental aspects of the ice surface and how it interacts with dopants. Even with the focus on adsorption of acidic trace gases to ice, results of this study will thus be of high relevance also for other chemical processes in ice and snow. This is of interest not only in environmental science but also in material science, cryobiology, and astrophysics.

  6. Electrochemical determination of tartaric acid at nano gold/nano carbon modified glassy carbon electrode

    NASA Astrophysics Data System (ADS)

    Song, Yang; Song, Yuanzhi; Xu, Jiang

    2012-09-01

    Nano gold/nano carbon coating the surface of glassy carbon electrode is prepared. Electrochemical behavior of tartaric acid at nano gold/graphene modified glassy carbon electrode is investigated. A simple, sensitive, and inexpensive method for determination of tartaric acid in drinks is proposed.

  7. Influence of sulfuric acid impregnation on the carbonization of cellulose

    NASA Astrophysics Data System (ADS)

    Kang, Kyu-Young; Kim, Dae-Young

    2012-05-01

    That cellulose, as source of carbon materials, has a low char yield in pyrolysis can present serious difficulties. In this study, we focused on the effect of using sulfuric acid as a dehydration agent and examined the pyrolytic behavior of cellulose impregnated with sulfuric acid by using thermogravimetry and scanning electron microscopy. The mass yield of carbon after an 800 °C treatment in nitrogen was increased by 2-5 times with the addition of small amounts of sulfuric acid. Sample shrinkage during carbonization was also significantly reduced. These effects are interpreted as being the result of facilitated extraction of water from cellulose accompanied by development of extended carbon networks.

  8. Carbonic Acid from Decarboxylation by Malic Enzyme in Lactic Acid Bacteria

    PubMed Central

    Pilone, Gordon J.; Kunkee, Ralph E.

    1970-01-01

    Carbonic anhydrase studies were used to determine the primary form of carbonic acid produced from decarboxylation of l-malic acid by malic enzyme in malolactic strains of five different species of lactic acid bacteria. Addition of carbonic anhydrase to the reaction mixture containing crude bacterial extract and l-malic acid, at pH 7, in all five cases resulted in an increase (13 to 23%) in the rate of carbon dioxide evolution over the control. The results indicated that the primary form of carbonic acid released from malic enzyme was not anhydrous carbon dioxide as previously supposed and as has been shown for other decarboxylating enzymes. The standard free-energy changes of the malo-lactic reaction with the various forms of carbonic acid as the primary decarboxylation product were calculated. The reaction is less exergonic when carbonic acid, bicarbonate ion, or carbonate ion is the primary decarboxylation product compared to anhydrous carbon dioxide. The free-energy of the reaction is not biologically available to the bacteria; with carbon dioxide not the primary decarboxylation product, the potential energy lost in a malo-lactic fermentation is not as great as previously considered. Endogenous carbonic anhydrase activity was not found. PMID:4988241

  9. In-vivo measurement of intrauterine gases and acid-base values early in human pregnancy.

    PubMed

    Jauniaux, E; Watson, A; Ozturk, O; Quick, D; Burton, G

    1999-11-01

    A new multiparameter sensor that combines electrochemical and fibre-optic technology was used for continuous in-vivo investigation of pH, carbon dioxide partial pressure (PCO(2)), oxygen partial pressure (PO(2)), bicarbonate concentration (HCO(3)(-)), base excess, and oxygen saturation (O(2)Sat) early in human pregnancy. The sensor was inserted into the amniotic cavity and the placental bed of 16 pregnancies at 10-15 weeks gestation, before termination under general anaesthesia. Amniotic fluid and retroplacental blood from the same site were also aspirated and analysed by means of cartridges and a portable blood gas analyser. Eleven series of measurements were obtained. The variation in measurements over the 5 min of monitoring was acid-base with a sensor is stable and accurate. Such technology will be helpful in improving our understanding of the fetoplacental metabolism in normal and complicated pregnancies. PMID:10548645

  10. Comparative Climate Responses of Anthropogenic Greenhouse Gases, All Major Aerosol Components, Black Carbon, and Methane, Accounting for the Evolution of the Aerosol Mixing State and of Clouds/Precipitation from Multiple Aerosol Size Distributions

    NASA Astrophysics Data System (ADS)

    Jacobson, M. Z.

    2005-12-01

    Several modeling studies to date have simulated the global climate response of anthropogenic greenhouse gases and bulk (non-size-resolved) sulfate or generic aerosol particles together, but no study has examined the climate response of greenhouse gases simultaneously with all major size- and composition resolved aerosol particle components. Such a study is important for improving our understanding of the effects of anthropogenic pollutants on climate. Here, the GATOR-GCMOM model is used to study the global climate response of (a) all major greenhouse gases and size-resolved aerosol components, (b) all major greenhouse gases alone, (c) fossil-fuel soot (black carbon, primary organic matter, sulfuric acid, bisulfate, sulfate), and (d) methane. Aerosol components treated in all simulations included water, black carbon, primary organic carbon, secondary organic carbon, sulfuric acid, bisulfate, sulfate, nitrate, chloride, ammonium, sodium, hydrogen ion, soil dust, and pollen/spores. Fossil-fuel soot (FFS) was emitted into its own size distribution. All other components, including biofuel and biomass soot, sea-spray, soil dust, etc., were emitted into a second distribution (MIX). The FFS distribution grew by condensation of secondary organic matter and sulfuric acid, hydration of water, and dissolution of nitric acid, ammonia, and hydrochloric acid. It self-coagulated and heterocoagulated with the MIX distribution, which also grew by condensation, hydration, and dissolution. Treatment of separate distributions for FFS allowed FFS to evolve from an external mixture to an internal mixture. In both distributions, black carbon was treated as a core component for optical calculations. Both aerosol distributions served as CCN during explicit size-resolved cloud formation. The resulting clouds grew by coagulation and condensation, coagulated with interstitial aerosol particles, and fell to the surface as rain and snow, carrying aerosol constituents with them. Thus, cloud evolution accounted for the first and second indirect effects and the mixing state of aerosol particles. The optical properties of clouds were found by treating black carbon inclusions surrounded by a shell of water. The albedos of snow, sea ice, and water were calculated with radiative transfer solutions, assuming black carbon inclusions in the case of snow and sea ice. The simulations accounted for 3-D energy diffusion to the deep ocean and 2-D ocean circulation. Major conclusions are (a) the most important constituents of global warming, in terms of climate response, appear to be, in order, carbon dioxide, black carbon, and methane, (b) aerosol particles (all together) appear to act on top of greenhouse gases to enhance extremes in both regional cooling and regional warming, (b) the combination of important greenhouse gases and aerosol particles can explain observed major regions of historic warming and cooling, and (d) eliminating all anthropogenic aerosol emission could more than double current global warming but would have less of an effect than independently doubling carbon dioxide.

  11. Removal potential of toxic 2378-substituted PCDD/F from incinerator flue gases by waste-derived activated carbons

    SciTech Connect

    Hajizadeh, Yaghoub; Onwudili, Jude A.; Williams, Paul T.

    2011-06-15

    The application of activated carbons has become a commonly used emission control protocol for the removal or adsorption of persistent organic pollutants from the flue gas streams of waste incinerators. In this study, the 2378-substituted PCDD/F removal efficiency of three types of activated carbons derived from the pyrolysis of refuse derived fuel, textile waste and scrap tyre was investigated and compared with that of a commercial carbon. Experiments were carried out in a laboratory scale fixed-bed reactor under a simulated flue gas at 275 deg. C with a reaction period of four days. The PCDD/F in the solid matrices and exhaust gas, were analyzed using gas chromatography coupled with a triple quadrupole mass spectrometer. In the absence of activated carbon adsorbent, there was a significant increase in the concentration of toxic PCDD/F produced in the reacted flyash, reaching up to 6.6 times higher than in the raw flyash. In addition, there was a substantial release of PCDD/F into the gas phase, which was found in the flue gas trapping system. By application of the different commercial, refuse derived fuel, textile and tyre activated carbons the total PCDD/F toxic equivalent removal efficiencies in the exhaust gas stream were 58%, 57%, 64% and 52%, respectively. In general, the removal of the PCDDs was much higher with an average of 85% compared to PCDFs at 41%. Analysis of the reacted activated carbons showed that there was some formation of PCDD/F, for instance, a total of 60.6 {mu}g I-TEQ kg{sup -1} toxic PCDD/F was formed in the refuse derived fuel activated carbon compared to 34 {mu}g I-TEQ kg{sup -1} in the commercial activated carbon. The activated carbons derived from the pyrolysis of waste, therefore, showed good potential as a control material for PCDD/F emissions in waste incinerator flue gases.

  12. The hyporheic zone as a source of dissolved organic carbon and carbon gases to a temperate forested stream

    USGS Publications Warehouse

    Schindler, J.E.; Krabbenhoft, D.P.

    1998-01-01

    The objective of this study was to examine chemical changes in porewaters that occur over small scales (cm) as groundwater flows through the hyporheic zone and discharges to a stream in a temperate forest of northern Wisconsin. Hyporheic-zone porewaters were sampled at discrete depths of 2, 10, 15, 61, and 183 cm at three study sites in the study basin. Chemical profiles of dissolved organic carbon (DOC), CO2, CH4, and pH show dramatic changes between 61 cm sediment depth and the water-sediment interface. Unless discrete samples at small depth intervals are taken, these chemical profiles are not accounted for. Similar trends were observed at the three study locations, despite each site having very different hydraulic-flow regimes. Increases in DOC concentration by an order of magnitude from 61 to 15 cm depth with a corresponding decrease in pH and rapid decreases in the molecular weight of the DOC suggest that aliphatic compounds (likely organic acids) are being generated in the hyporheic zone. Estimated efflux rates of DOC, CO2, and CH4 to the stream are 6.2, 0.79, 0.13 moles m2 d-1, respectively, with the vast majority of these materials produced in the hyporheic zone. Very little of these materials are accounted for by sampling stream water, suggesting rapid uptake and/or volatilization.

  13. Apparatus for purifying arsine, phosphine, ammonia, and inert gases to remove Lewis acid and oxidant impurities therefrom

    DOEpatents

    Tom, Glenn M.; Brown, Duncan W.

    1991-01-08

    An apparatus for purifying a gaseous mixture comprising arsine, phosphine, ammonia, and/or inert gases, to remove Lewis acid and/or oxidant impurities therefrom, comprising a vessel containing a bed of a scavenger, the scavenger including a support having associated therewith an anion which is effective to remove such impurities, such anion being selected from one or more members of the group consisting of: (i) carbanions whose corresponding protonated compounds have a pK.sub.a value of from about 22 to about 36; and (ii) anions formed by reaction of such carbanions with the primary component of the mixture.

  14. Opportunities for Coordinated Observations of CO2 with the Orbiting Carbon Observatory (OCO) and Greenhouse Gases Observing Satellite (GOSAT)

    NASA Technical Reports Server (NTRS)

    Crisp, David

    2008-01-01

    The Orbiting Carbon Observatory (OCO) and the Greenhouse Gases Observing Satellite (GOSAT) are the first two satellites designed to make global measurements of atmospheric carbon dioxide (CO2) with the precision and sampling needed identify and monitor surface sources and sinks of this important greenhouse gas. Because the operational phases of the OCO and GOSAT missions overlap in time, there are numerous opportunities for comparing and combining the data from these two satellites to improve our understanding of the natural processes and human activities that control the atmospheric CO2 and it variability over time. Opportunities for cross-calibration, cross-validation, and coordinated observations that are currently under consideration are summarized here.

  15. Potential effects of clean coal technologies on acid precipitation, greenhouse gases, and solid waste disposal

    SciTech Connect

    Blasing, T.J.; Miller, R.L.; McCold, L.N.

    1993-11-01

    The US Department of Energy`s (DOE`s) Clean Coal Technology Demonstration Program (CCTDP) was initially funded by Congress to demonstrate more efficient, economically feasible, and environmentally acceptable coal technologies. Although the environmental focus at first was on sulfur dioxide (SO{sub 2}) and nitrogen oxides (NO{sub x}) because their relationship to acid precipitation, the CCTDP may also lead to reductions in carbon dioxide (CO{sub 2}) emissions and in the volume of solid waste produced, compared with conventional technologies. The environmental effects of clean coal technologies (CCTs) depend upon which (if any) specific technologies eventually achieve high acceptance in the marketplace. In general, the repowering technologies and a small group of retrofit technologies show the most promise for reducing C0{sub 2} emissions and solid waste. These technologies also compare favorably with other CCTs in terms of SO{sub 2} and NO{sub x} reductions. The upper bound for CO{sup 2} reductions in the year 2010 is only enough to reduce global ``greenhouse`` warming potential by about 1%. However, CO{sub 2} emissions come from such variety of sources around the globe that no single technological innovation or national policy change could realistically be expected to reduce these emissions by more than a few percent. Particular CCTs can lead to either increases or decreases in the amount of solid waste produced. However, even if decreases are not achieved, much of the solid waste from clean coal technologies would be dry and therefore easier to dispose of than scrubber sludge.

  16. Carbon Dioxide Information Analysis Center and World Data Center-A for atmospheric trace gases: FY 1993 activities

    SciTech Connect

    Cushman, R.M.; Stoss, F.W. |

    1994-01-01

    During the course of a fiscal year, Oak Ridge National Laboratory`s Carbon Dioxide Information Analysis Center (CDIAC) distributes thousands of specialty publications-numeric data packages (NDPs), computer model packages (CMPs), technical reports, public communication publications, newsletters, article reprints, and reference books-in response to requests for information related to global environmental issues, primarily those pertaining to climate change. CDIAC`s staff also provide technical responses to specific inquiries related to carbon dioxide (CO{sub 2}), other trace gases, and climate. Hundreds of referrals to other researchers, policy analysts, information specialists, or organizations are also facilitated by CDIAC`s staff. This report provides an account of the activities accomplished by CDIAC (including World Data Center-A for Atmospheric Trace Gases) during the period October 1, 1992, to September 30, 1993. An organizational overview of CDIAC and its staff is supplemented by a detailed description of inquiries received and CDIAC`s response to those inquiries. An analysis and description of the preparation and distribution of NDPS, CMPS, technical reports, newsletters, fact sheets, specialty publications, and reprints are provided. Comments and descriptions of CDIAC`s information management systems, professional networking, and special bilateral agreements are also presented.

  17. Biological production of ethanol from waste gases with Clostridium ljungdahlii

    DOEpatents

    Gaddy, James L. (Fayetteville, AR)

    2000-01-01

    A method and apparatus for converting waste gases from industrial processes such as oil refining, carbon black, coke, ammonia, and methanol production, into useful products is disclosed. The method includes introducing the waste gases into a bioreactor where they are fermented to various product, such as organic acids, alcohols H.sub.2, SCP, and salts of organic acids by anaerobic bacteria within the bioreactor. These valuable end products are then recovered, separated and purified.

  18. Reduction of Plutonium in Acidic Solutions by Mesoporous Carbons

    DOE PAGESBeta

    Parsons-Moss, Tashi; Jones, Stephen; Wang, Jinxiu; Wu, Zhangxiong; Uribe, Eva; Zhao, Dongyuan; Nitsche, Heino

    2015-12-19

    Batch contact experiments with several porous carbon materials showed that carbon solids spontaneously reduce the oxidation state of plutonium in 1-1.5 M acid solutions, without significant adsorption. The final oxidation state and rate of Pu reduction varies with the solution matrix, and also depends on the surface chemistry and surface area of the carbon. It was demonstrated that acidic Pu(VI) solutions can be reduced to Pu(III) by passing through a column of porous carbon particles, offering an easy alternative to electrolysis with a potentiostat.

  19. High rate chemical vapor deposition of carbon films using fluorinated gases

    DOEpatents

    Stafford, Byron L. (Arvada, CO); Tracy, C. Edwin (Golden, CO); Benson, David K. (Golden, CO); Nelson, Arthur J. (Longmont, CO)

    1993-01-01

    A high rate, low-temperature deposition of amorphous carbon films is produced by PE-CVD in the presence of a fluorinated or other halide gas. The deposition can be performed at less than 100.degree. C., including ambient room temperature, with a radio frequency plasma assisted chemical vapor deposition process. With less than 6.5 atomic percent fluorine incorporated into the amorphous carbon film, the characteristics of the carbon film, including index of refraction, mass density, optical clarity, and chemical resistance are within fifteen percent (15%) of those characteristics for pure amorphous carbon films, but the deposition rates are high.

  20. Meldrum's acids and 5-alkylidene Meldrum's acids in catalytic carbon-carbon bond-forming processes.

    PubMed

    Dumas, Aaron M; Fillion, Eric

    2010-03-16

    Meldrum's acid (2,2-dimethyl-1,3-dioxane-4,6-dione) is a molecule with a unique history, owing to its originally misassigned structure, as well as a unique place among acylating agents, owing to its high acidity and remarkable electrophilicity. In this Account, we outline the work of our group and others toward harnessing the reactivity of Meldrum's acid derivatives in catalytic C-C bond-forming reactions. Taking advantage of the ability of Meldrum's acid to decompose to CO(2) and acetone following acyl substitution, we have shown that intramolecular Friedel-Crafts acylations can be performed under mild Lewis acidic conditions to yield a variety of benzocyclic ketones. In a further expansion of this method, a domino Friedel-Crafts acylation/alpha-tert alkylation reaction was used to complete the first total synthesis of (+/-)-taiwaniaquinol B. The unique characteristics of Meldrum's acid extend to its alkylidene derivatives, which have also proven exceptionally useful for the development of new reactions not readily accessible from other unsaturated carbonyl electrophiles. By combining the electrophilicity and dienophilicity of alkylidene Meldrum's acid with our Friedel-Crafts chemistry, we have demonstrated new domino syntheses of coumarin derivatives and tetrahydrofluorenones by conjugate additions, Diels-Alder cycloadditions, and C-H functionalizations. Additionally, we have used these powerful acceptors to allow conjugate alkenylation with functionalized organostannanes, and conjugate allylation under very mild conditions. We have also shown that these molecules permit the asymmetric formation of all-carbon quaternary stereocenters via enantioselective conjugate additions. These reactions employ dialkylzinc nucleophiles, maximizing functional group compatibility, while the presence of a Meldrum's acid moiety in the product allows a variety of postaddition modifications. A full investigation of this reaction has determined the structural factors of the alkylidene that contribute to optimal enantioselectivity. We have also used these acceptors to form tertiary propargylic stereocenters in very high enantiomeric excess by an extremely mild, Rh(I)-catalyzed addition of TMS-acetylene. Overall, we demonstrate that Meldrum's acid and its derivatives provide access to a broad range of reactivities that, combined with their ease of handling and preparation, make them ideal electrophiles. PMID:20000793

  1. Procedures for safe handling of off-gases from electric vehicle lead-acid batteries during overcharge

    SciTech Connect

    LaBelle, S.J.; Bhattacharyya, M.H.; Loutfy, R.O.; Varma, R.

    1980-01-25

    The potential for generation of toxic gases from lead-acid batteries has long been recognized. Prior to the current interest in electric vehicles, there were no studies specificaly oriented to toxic gas release from traction batteries, however. As the Department of Energy Demonstration Project (in the Electric and Hybrid Vehicle Program) progresses, available data from past studies and parallel health effects programs must be digested into guidance to the drivers and maintenance personnel, tailored to their contact with electric vehicles. The basic aspects of lead-acid battery operation, vehicle use, and health effects of stibine and arsine to provide electric vehicle users with the information behind the judgment that vehicle operation and testing may proceed are presented. Specifically, it is concluded that stibine generation or arsine generation at rapid enough rates to induce acute toxic response is not at all likely. Procedures to guard against low-level exposure until more definitive data on ambient concentrations of the gases are collected are presented for both charging the batteries and driving the vehicles. A research plan to collect additional quantitative data from electric traction batteries is presented.

  2. Separation of H2S and NH3 gases from tofu waste water-based biogas using activated carbon adsorption

    NASA Astrophysics Data System (ADS)

    Harihastuti, Nani; Purwanto, P.; Istadi, I.

    2015-12-01

    Research on the separation of H2S and NH3 gases from tofu waste water-based biogas has been conducted to improve the content of CH4 of biogas in order to increase calorific value. Biogas from tofu waste water contained many kinds of gases such as: CH4 of 53-64%, CO2 of 36-45%, H2S of 3,724-5,880 mg/Nm3, NH3 of 0.19-70.36 mg/Nm3, and H2O of 33,800-19,770,000 mg/Nm3. In fact, CO2, H2S, NH3, and moisture are impurities that have disturbance to human and environment, so that they are necessary to be separated from biogas. Particularly, H2S and NH3 have high toxicity to people, particularly the workers in the tofu industry. Therefore, separation of H2S and NH3 from biogas to increase calorific value is the focus of this research. The method used in this research is by adsorption of H2S and NH3 gases using activated carbon as adsorbent. It also used condensation as pretreatment to remove moisture content in biogas. Biogas was flowed to adsorption column (70 cm height and 9 cm diameter containing activated carbon as much as 500 g) so that the H2S and NH3 gases were adsorbed. This research was conducted by varying flow rate and flow time of biogas. From this experiment, it was found that the optimum adsorption conditions were flow rate of 3.5 l/min and 4 hours flow time. This condition could reach 99.95% adsorption efficiency of H2S from 5,879.50 mg/Nm3 to 0.67 mg/Nm3, and 74.96% adsorption efficiency of NH3 from 2.93 mg/Nm3 to 0.73 mg/Nm3. The concentration of CH4 increased from 63.88% to 76.24% in the biogas.

  3. Sea salt aerosols as a reactive surface for inorganic and organic acidic gases in the Arctic troposphere

    NASA Astrophysics Data System (ADS)

    Chi, J. W.; Li, W. J.; Zhang, D. Z.; Zhang, J. C.; Lin, Y. T.; Shen, X. J.; Sun, J. Y.; Chen, J. M.; Zhang, X. Y.; Zhang, Y. M.; Wang, W. X.

    2015-10-01

    Sea salt aerosols (SSA) are dominant particles in the Arctic atmosphere and determine the polar radiative balance. SSA react with acidic pollutants that lead to changes in physical and chemical properties of their surface, which in turn alter their hygroscopic and optical properties. Transmission electron microscopy with energy-dispersive X-ray spectrometry was used to analyze morphology, composition, size, and mixing state of individual SSA at Ny-Ålesund, Svalbard, in summertime. Individual fresh SSA contained cubic NaCl coated by certain amounts of MgCl2 and CaSO4. Individual partially aged SSA contained irregular NaCl coated by a mixture of NaNO3, Na2SO4, Mg(NO3)2, and MgSO4. The comparison suggests the hydrophilic MgCl2 coating in fresh SSA likely intrigued the heterogeneous reactions at the beginning of SSA and acidic gases. Individual fully aged SSA normally had Na2SO4 cores and an amorphous coating of NaNO3. Elemental mappings of individual SSA particles revealed that as the particles ageing Cl gradually decreased, the C, N, O, and S content increased. 12C- mapping from nanoscale secondary ion mass spectrometry indicates that organic matter increased in the aged SSA compared with the fresh SSA. 12C- line scan further shows that organic matter was mainly concentrated on the aged SSA surface. These new findings indicate that this mixture of organic matter and NaNO3 on particle surfaces likely determines their hygroscopic and optical properties. These abundant SSA as reactive surfaces adsorbing inorganic and organic acidic gases can shorten acidic gas lifetime and influence the possible gaseous reactions in the Arctic atmosphere, which need to be incorporated into atmospheric chemical models in the Arctic troposphere.

  4. Nature of the carbon and sulfur phases and inorganic gases in the Kenna ureilite

    NASA Technical Reports Server (NTRS)

    Gibson, E. K., Jr.

    1976-01-01

    Abundances of carbon and sulfur in the Kenna ureilite are 2.219 plus or minus 0.060 wt. % C and 0.179 plus or minus 0.008 wt. % S. Secondary carbonates resulting from terrestrial weathering account for 0.25 plus or minus 0.02 wt. % C. No hydrocarbons were detected during gas release measurements. Most of the carbon is in graphite, diamond, or lonsdaleite. The sample of Kenna contained 0.95 plus or minus 0.05 wt.% H2O. Total carbon and sulfur measurements were made on three additional ureilites: Havero, Dingo Pup Donga, and North Haig. Ureilite carbon abundances are similar to those of C-2 chondrites, whereas sulfur abundances are a factor of 10 less than C-2 chondrites and ordinary chondrites. The elemental abundances, ratios, and phases present in the ureilites rule out a direct genetic relationship between the ureilites and the carbonaceous chondrites.

  5. Influence of inert gases on the reactive high power pulsed magnetron sputtering process of carbon-nitride thin films

    SciTech Connect

    Schmidt, Susann; Czigany, Zsolt; Greczynski, Grzegorz; Jensen, Jens; Hultman, Lars

    2013-01-15

    The influence of inert gases (Ne, Ar, Kr) on the sputter process of carbon and carbon-nitride (CN{sub x}) thin films was studied using reactive high power pulsed magnetron sputtering (HiPIMS). Thin solid films were synthesized in an industrial deposition chamber from a graphite target. The peak target current during HiPIMS processing was found to decrease with increasing inert gas mass. Time averaged and time resolved ion mass spectroscopy showed that the addition of nitrogen, as reactive gas, resulted in less energetic ion species for processes employing Ne, whereas the opposite was noticed when Ar or Kr were employed as inert gas. Processes in nonreactive ambient showed generally lower total ion fluxes for the three different inert gases. As soon as N{sub 2} was introduced into the process, the deposition rates for Ne and Ar-containing processes increased significantly. The reactive Kr-process, in contrast, showed slightly lower deposition rates than the nonreactive. The resulting thin films were characterized regarding their bonding and microstructure by x-ray photoelectron spectroscopy and transmission electron microscopy. Reactively deposited CN{sub x} thin films in Ar and Kr ambient exhibited an ordering toward a fullerene-like structure, whereas carbon and CN{sub x} films deposited in Ne atmosphere were found to be amorphous. This is attributed to an elevated amount of highly energetic particles observed during ion mass spectrometry and indicated by high peak target currents in Ne-containing processes. These results are discussed with respect to the current understanding of the structural evolution of a-C and CN{sub x} thin films.

  6. Carbon-based strong solid acid for cornstarch hydrolysis

    NASA Astrophysics Data System (ADS)

    Nata, Iryanti Fatyasari; Irawan, Chairul; Mardina, Primata; Lee, Cheng-Kang

    2015-10-01

    Highly sulfonated carbonaceous spheres with diameter of 100-500 nm can be generated by hydrothermal carbonization of glucose in the presence of hydroxyethylsulfonic acid and acrylic acid at 180 °C for 4 h. The acidity of the prepared carbonaceous sphere C4-SO3H can reach 2.10 mmol/g. It was used as a solid acid catalyst for the hydrolysis of cornstarch. Total reducing sugar (TRS) concentration of 19.91 mg/mL could be obtained by hydrolyzing 20 mg/mL cornstarch at 150 °C for 6 h using C4-SO3H as solid acid catalyst. The solid acid catalyst demonstrated good stability that only 9% decrease in TRS concentration was observed after five repeat uses. The as-prepared carbon-based solid acid catalyst can be an environmentally benign replacement for homogeneous catalyst.

  7. Trends in source gases

    NASA Technical Reports Server (NTRS)

    Ehhalt, D. H.; Fraser, P. J.; Albritton, D.; Cicerone, R. J.; Khalil, M. A. K.; Legrand, M.; Makide, Y.; Rowland, F. S.; Steele, L. P.; Zander, R.

    1989-01-01

    Source gases are defined as those gases that, by their breakdown, introduce into the stratosphere halogen, hydrogen, and nitrogen compounds that are important in stratospheric ozone destruction. Given here is an update of the existing concentration time series for chlorocarbons, nitrous oxide, and methane. Also reviewed is information on halogen containing species and the use of these data for establishing trends. Also reviewed is evidence on trends in trace gases that influence tropospheric chemistry and thus the tropospheric lifetimes of source gases, such as carbon dioxide, carbon monoxide, or nitrogen oxides. Much of the information is given in tabular form.

  8. Postcombustion measures for cleaner solid fuels combustion: activated carbons for toxic pollutants removal from flue gases

    SciTech Connect

    G. Skodras; I. Diamantopoulou; P. Natas; A. Palladas; G.P. Sakellaropoulos

    2005-12-01

    In this work the efficiency of postcombustion measures (i.e., activated carbon utilization) to achieve cleaner solid fuels combustion was evaluated. Thus, two commercial activated carbons (Calgon F400 and RWE active coke) were tested for removing toxic polluting compounds (Hg, PCBs, PCDD/Fs) from the gas phase. The effects of the pore structure and surface chemistry of the activated carbons tested were investigated, along with the sorption temperature and sulfur addition in carbon matrix. Experiments were realized in a bench-scale adsorption unit and in a commercial solid fuels-fired hot water boiler. The results showed that both activated carbons tested are suitable for the removal of toxic compounds (i.e., Hg, PCBs, PCDD/Fs) from the gas phase. Due to differences in Hg adsorptive capacity and adsorption rate, which are attributed to the diversified pore structure and surface chemistry of the activated carbons, RWE active coke is, presumably, more suitable for continuous Hg removal (i.e., activated carbon injection), while Calgon F400 is more suitable for batch one (packed column). For both activated carbons, Hg adsorption capacity was reduced with temperature increase, while it was enhanced by the presence of sulfur. Oxygen surface functional groups seem to be involved in Hg adsorption mechanism. Lactones are believed to act as potential active sites for mercury adsorption, while phenols may act as inhibitors. The removal of PCBs and PCDD/Fs from the gas phase seems not to be a problem for the activated carbons tested, regardless of their pore structure or surface chemistry. 61 refs., 23 figs., 8 tabs.

  9. Nitric acid vapor removal by activated, impregnated carbons

    SciTech Connect

    Wood, G.O.

    1996-12-31

    Laboratory and industrial workers can be exposed to vapors of nitric acid, especially in accidents, such as spills. Nitric acid can also be a product of incineration for energy production or waste (e.g., CW agent) disposal. Activated carbons containing impregnants for enhancing vapor and gas removal have been tested for effectiveness in removing vapors of nitric acid from air. The nitric acid vapor was generated from concentrated acid solutions and detected by trapping in a water bubbler for pH measurements. Both low and moderate relative humidity conditions were used. All carbons were effective at vapor contact times representative of air-purifying respirator use. One surprising observation was the desorption of low levels of ammonia from impregnated carbons. This was apparently due to residual ammonia from the impregnation processes.

  10. Sorption of noble gases by solids, with reference to meteorites. I - Magnetite and carbon

    NASA Technical Reports Server (NTRS)

    Yang, J.; Lewis, R. S.; Anders, E.

    1982-01-01

    The trapping of meteoritic noble gases by solids is simulated through the synthesis of 18 Fe3O4 samples at 350-720 K in a noble gas atmosphere, by means of the reactions: (1) 3Fe + 4H2O yields Fe3O4 + 4H2, using Ne, Ar, Kr and Xe; and (2) 3Fe + 4CO yields Fe3O4 + 4C + carbides, using Xe. Etching experiments suggest an analogy with 'Phase Q' in meteorites. Adsorbed atmospheric gases are present in all samples, and dominate whenever the noble gas partial pressure in the atmosphere is greater than that in the synthesis. While many of the results of Lancet and Anders (1973) appear to have been dominated by such an atmospheric component, others are suspect. When the doubtful samples of Lancet and Anders are corrected or eliminated, the fractionation pattern no longer peaks at Ar, but rather, as in the present sample, rises monotonically from Ne to Xe. No evidence is found for the earlier study's claim of a strong temperature dependence.

  11. Sorption of noble gases by solids, with reference to meteorites. I - Magnetite and carbon

    NASA Astrophysics Data System (ADS)

    Yang, J.; Lewis, R. S.; Anders, E.

    1982-06-01

    The trapping of meteoritic noble gases by solids is simulated through the synthesis of 18 Fe3O4 samples at 350-720 K in a noble gas atmosphere, by means of the reactions: (1) 3Fe + 4H2O yields Fe3O4 + 4H2, using Ne, Ar, Kr and Xe; and (2) 3Fe + 4CO yields Fe3O4 + 4C + carbides, using Xe. Etching experiments suggest an analogy with 'Phase Q' in meteorites. Adsorbed atmospheric gases are present in all samples, and dominate whenever the noble gas partial pressure in the atmosphere is greater than that in the synthesis. While many of the results of Lancet and Anders (1973) appear to have been dominated by such an atmospheric component, others are suspect. When the doubtful samples of Lancet and Anders are corrected or eliminated, the fractionation pattern no longer peaks at Ar, but rather, as in the present sample, rises monotonically from Ne to Xe. No evidence is found for the earlier study's claim of a strong temperature dependence.

  12. Measurements of Acetic Acid and its Relationships with Trace Gases on Appledore Island, ME during the ICARTT Campaign

    NASA Astrophysics Data System (ADS)

    Haase, K. B.; Sive, B. C.; White, M. L.; Russo, R. S.; Ambrose, J. L.; Zhou, Y.; Talbot, R. W.

    2011-12-01

    Acetic acid is ubiquitously present in the ambient atmosphere. Acetic acid, along with formic acid, is the one of the most abundant gas phase organic acids with mixing ratios reaching into the tens of parts per billion by volume (ppbv) range, and can influence the pH of aerosols and precipitation. The magnitude of the sources and sinks of acetic acid in the environment is not well understood (~24 Tg/yr of missing emissions globally), as they are widely dispersed and measurements are relatively challenging to accomplish using established techniques. Here, the application of Proton Transfer Reaction Mass Spectrometry (PTR-MS) is explored as a technique for quantification of ambient acetic acid. Direct calibrations of PTR-MS instruments at low ppbv levels show good linearity and fast response, and during the ICARTT campaign, a PTR-MS measured acetic acid and a suite of other volatile organic compounds on Appledore Island, ME over a period of 6 weeks. During the campaign, the average mixing ratio of acetic acid on the island was 607.9 341.8 (1?) pptv with a median of 530 pptv. Mixing ratios of acetic acid observed on the island showed diurnal variations corresponding land breeze/sea breeze transport, similar to other pollutants including ozone and carbon monoxide, indicating that acetic acid was advected to the sample site, and not a product of local emissions. Additionally, no mixing ratio dependence on wind speed was found, indicating that at this location, loss due to dry deposition to the ocean during transport was minimal. Over the course of the campaign, acetic acid showed complex relationships with a range of other VOCs, indicating a diverse set of sources and further showing the utility of the PTR-MS technique for monitoring acetic acid. Mixing ratios of acetic acid showed correlations with different compounds at different times, indicating a complex source signature comprised of (1) anthropogenic emissions, (2) biomass burning, and (3) photochemical sources. Evidence of anthropogenic sources of acetic acid is shown by correlations with acetaldehyde, ethane, ethyne, dichloroethene, and carbon monoxide. Combustion emissions of carbon monoxide show the possibility of using carbon monoxide as tracer of acetic acid levels, yielding an enhancement ratio of 8.71 0.54 pptv ppbv-1 of carbon monoxide. Acetic acid mixing ratios were also higher when acetonitrile mixing ratios were elevated, indicating contributions from a biomass combustion source. Mixing ratios of alkyl nitrates also trended with acetic acid at times, indicating periods when contributions from photochemical production and transport in aged air masses were likely. Major Funding: NOAA Office of Oceanic and Atmospheric Research under grant # NA04OAR4600154, and the USGS for the opportunity to present the data.

  13. The Strongest Acid: Protonation of Carbon Dioxide.

    PubMed

    Cummings, Steven; Hratchian, Hrant P; Reed, Christopher A

    2016-01-01

    The strongest carborane acid, H(CHB11 F11 ), protonates CO2 while traditional mixed Lewis/Brønsted superacids do not. The product is deduced from IR spectroscopy and calculation to be the proton disolvate, H(CO2 )2 (+) . The carborane acid H(CHB11 F11 ) is therefore the strongest known acid. The failure of traditional mixed superacids to protonate weak bases such as CO2 can be traced to a competition between the proton and the Lewis acid for the added base. The high protic acidity promised by large absolute values of the Hammett acidity function (H0 ) is not realized in practice because the basicity of an added base is suppressed by Lewis acid/base adduct formation. PMID:26663640

  14. Sea salt aerosols as a reactive surface for inorganic and organic acidic gases in the arctic troposphere

    NASA Astrophysics Data System (ADS)

    Chi, J. W.; Li, W. J.; Zhang, D. Z.; Zhang, J. C.; Lin, Y. T.; Shen, X. J.; Sun, J. Y.; Chen, J. M.; Zhang, X. Y.; Zhang, Y. M.; Wang, W. X.

    2015-06-01

    Sea salt aerosols (SSA) are dominant particles in the arctic atmosphere and determine the polar radiative balance. SSA react with acidic pollutants that lead to changes of physical and chemical properties of their surface, which in turn alter their hygroscopic and optical properties. Transmission electron microscopy with energy-dispersive X-ray spectrometry was used to analyze morphology, composition, size, and mixing state of individual SSA at Ny-Ålesund, Svalbard in summertime. Individual fresh SSA contained cubic NaCl coated by certain amounts of MgCl2 and CaSO4. Individual partially aged SSA contained irregular NaCl coated by a mixture of NaNO3, Na2SO4, Mg(NO3)2, and MgSO4. The comparison suggests the hydrophilic MgCl2 coating in fresh SSA likely intrigued the heterogeneous reactions at the beginning of SSA and acidic gases. Individual fully aged SSA normally had Na2SO4 cores and an amorphous coating of NaNO3. Elemental mappings of individual SSA particles revealed that as the particles ageing Cl gradually decreased but the C, N, O, and S content increased. 12C14N- mapping from nanoscale secondary ion mass spectrometry indicates that organic matter increased in the aged SSA compared with the fresh SSA. 12C14N- line scans further show that organic matter was mainly concentrated on the aged SSA surface. These new findings indicate that this mixture of organic matter and NaNO3 on particle surfaces determines their hygroscopic and optical properties. These abundant SSA, whose reactive surfaces absorb inorganic and organic acidic gases in the arctic troposphere, need to be incorporated into atmospheric chemical models.

  15. Determination of the acidic sites of purified single-walled carbon nanotubes by acid base titration

    NASA Astrophysics Data System (ADS)

    Hu, H.; Bhowmik, P.; Zhao, B.; Hamon, M. A.; Itkis, M. E.; Haddon, R. C.

    2001-09-01

    We report the measurement of the acidic sites in three different samples of commercially available full-length purified single-walled carbon nanotubes (SWNTs) - as obtained from CarboLex (CLI), Carbon Solutions (CSI) and Tubes@Rice (TAR) - by simple acid-base titration methods. Titration of the purified SWNTs with NaOH and NaHCO 3 solutions was used to determine the total percentage of acidic sites and carboxylic acid groups, respectively. The total percentage of acidic sites in full length purified SWNTs from TAR, CLI and CSI are about 1-3%.

  16. Laboratory shock emplacement of noble gases, nitrogen, and carbon dioxide into basalt, and implications for trapped gases in shergottite EETA 79001

    SciTech Connect

    Wiens, R.C.; Pepin, R.O.

    1988-02-01

    Basalt samples have been analyzed mass spectrometrically for shock-implanted noble gases, N/sub 2/, and CO/sub 2/ after exposure to 20-60 GPa (200-600 kbar) shock in the presence of .0045-3.0 atm of ambient gas. Abundances of emplaced gases varied linearly with ambient gas pressure for constant shock pressure, and gas emplacement was most efficient in the range of 35-50 GPa shock pressure. Uncrushed samples shocked in this range gave emplacement efficiencies of 2.0-6.7% for heavy noble gases and nitrogen, while powdered samples with higher effective porosity yielded 40-50% efficiencies, indicating that approx. 50% of noble gases and nitrogen available in pores paces was emplaced. No elemental or isotopic fractionation was detected with Ar, Kr, Xe, or N/sub 2/. Helium and, in some samples, Ne were lost by diffusions subsequent to shock. Emplacement efficiencies for CO/sub 2/ averaged a factor of 1.8 +/- 0.2 greater than those of N/sub 2/ and noble gases in 4 samples with 20-50 GPa shock, and yielded 3.2 times greater efficiency in a sample shocked to 60 GPa. Enhanced CO/sub 2/ emplacement is thought to be due to reaction with silicate materials. Trapped gases in EETA 79001 glass were probably emplaced by shock. However, apparent emplacement efficiencies are somewhat higher than even shocked powder samples. Possible explanations for the difference include atmospheric overpressure at the time of shock, trapping of gas already in vugs by intruding melt material, or collapse of gas-filled vugs to form gas-laden glass inclusions.

  17. Carbon Dioxide Information Analysis Center and World Data Center for Atmospheric Trace Gases Fiscal Year 1999 Annual Report

    SciTech Connect

    Cushman, R.M.

    2000-03-31

    The Carbon Dioxide Information Analysis Center (CDIAC), which includes the World Data Center (WDC) for Atmospheric Trace Gases, is the primary global-change data and information analysis center of the Department of Energy (DOE). More than just an archive of data sets and publications, CDIAC has--since its inception in 1982--enhanced the value of its holdings through intensive quality assurance, documentation, and integration. Whereas many traditional data centers are discipline-based (for example, meteorology or oceanography), CDIAC's scope includes potentially anything and everything that would be of value to users concerned with the greenhouse effect and global climate change, including concentrations of carbon dioxide (CO{sub 2}) and other radiatively active gases in the atmosphere; the role of the terrestrial biosphere and the oceans in the biogeochemical cycles of greenhouse gases; emissions of CO{sub 2} and other trace gases to the atmosphere; long-term climate trends; the effects of elevated CO{sub 2} on vegetation; and the vulnerability of coastal areas to rising sea level. CDIAC is located within the Environmental Sciences Division (ESD) at Oak Ridge National Laboratory (ORNL) in Oak Ridge, Tennessee. CDIAC is co-located with ESD researchers investigating global-change topics, such as the global carbon cycle and the effects of carbon dioxide on vegetation. CDIAC staff are also connected with current ORNL research on related topics, such as renewable energy and supercomputing technologies. CDIAC is supported by the Environmental Sciences Division (Jerry Elwood, Acting Director) of DOE's Office of Biological and Environmental Research. CDIAC's FY 1999 budget was 2.2M dollars. CDIAC represents the DOE in the multi-agency Global Change Data and Information System. Bobbi Parra, and Wanda Ferrell on an interim basis, is DOE's Program Manager with responsibility for CDIAC. CDIAC comprises three groups, Global Change Data, Computer Systems, and Information Services, with seventeen full-time and part-time staff. The Global Change Data group is responsible for identifying and obtaining databases important to global-change research, analyzing data, compiling needed databases, providing data management support to specific programs (e.g., NARSTO), and preparing documentation to ensure the long-term utility of CDIAC's data holdings. The Computer Systems group provides computer system support for all CDIAC and WDC activities, including designing and maintaining CDIAC's computing system network; ensuring compliance with ORNL/DOE computing security regulations; ensuring long-term preservation of CDIAC data holdings through systematic backups; evaluating, developing, and implementing software; ensuring standards compliance; generating user statistics; providing Web design, development, and oversight; and providing systems analysis and programming assistance for scientific data projects. The Information Services group responds to data and information requests; maintains records of all request activities; assists in Web development and maintenance; and produces CDIAC's newsletter, CDIAC Communications, catalog, glossary, and educational materials. The following section provides further details on CDIAC's organization.

  18. Carbon Dioxide Information Analysis Center and World Data Center for Atmospheric Trace Gases Fiscal Year 2001 Annual Report

    SciTech Connect

    Cushman, R.M.

    2002-10-15

    The Carbon Dioxide Information Analysis Center (CDIAC), which includes the World Data Center (WDC) for Atmospheric Trace Gases, is the primary global change data and information analysis center of the U.S. Department of Energy (DOE). More than just an archive of data sets and publications, CDIAC has, since its inception in 1982, enhanced the value of its holdings through intensive quality assurance, documentation, and integration. Whereas many traditional data centers are discipline-based (for example, meteorology or oceanography), CDIAC's scope includes potentially anything and everything that would be of value to users concerned with the greenhouse effect and global climate change, including concentrations of carbon dioxide (CO{sub 2}) and other radiatively active gases in the atmosphere; the role of the terrestrial biosphere and the oceans in the biogeochemical cycles of greenhouse gases; emissions of CO{sub 2} and other trace gases to the atmosphere; long-term climate trends; the effects of elevated CO{sub 2} on vegetation; and the vulnerability of coastal areas to rising sea levels. CDIAC is located within the Environmental Sciences Division (ESD) at Oak Ridge National Laboratory (ORNL) in Oak Ridge, Tennessee. CDIAC is co-located with ESD researchers investigating global-change topics, such as the global carbon cycle and the effects of carbon dioxide on climate and vegetation. CDIAC staff are also connected with current ORNL research on related topics, such as renewable energy and supercomputing technologies. CDIAC is supported by the Environmental Sciences Division (Jerry Elwood, Director) of DOE's Office of Biological and Environmental Research. CDIAC represents DOE in the multi-agency Global Change Data and Information System (GCDIS). Wanda Ferrell is DOE's Program Manager with overall responsibility for CDIAC. Roger Dahlman is responsible for CDIAC's AmeriFlux tasks, and Anna Palmisano for CDIAC's Ocean Data tasks. CDIAC is made up of three groups: Data Systems, Information Services, and Computer Systems, with nineteen full-time or part-time staff. The following section provides details on CDIAC's staff and organization. The Data Systems Group identifies and obtains databases important to global-change research; analyzes data; compiles needed databases; provides data management and support to specific programs [e.g., NARSTO, Free-Air CO{sub 2} Enrichment (FACE), AmeriFlux, Oceans]; and prepares documentation to ensure the long-term utility of CDIAC's data holdings. The Information Services Group responds to data and information requests; maintains records of all request activities; analyzes user statistics; assists in Web development and maintenance; and produces CDIAC's newsletter (CDIAC Communications), the fiscal year annual reports, and various information materials. The Computer Systems Group provides computer system support for all CDIAC and WDC activities; designs and maintains CDIAC's computing system network; ensures compliance with ORNL/DOE computing security regulations; ensures long-term preservation of CDIAC data holdings through systematic backups; evaluates, develops, and implements software; ensures standards compliance; generates user statistics; provides Web design, development, and oversight; and provides systems analysis and programming assistance for scientific data projects.

  19. Swellable, water- and acid-tolerant polymer sponges for chemoselective carbon dioxide capture.

    PubMed

    Woodward, Robert T; Stevens, Lee A; Dawson, Robert; Vijayaraghavan, Meera; Hasell, Tom; Silverwood, Ian P; Ewing, Andrew V; Ratvijitvech, Thanchanok; Exley, Jason D; Chong, Samantha Y; Blanc, Frédéric; Adams, Dave J; Kazarian, Sergei G; Snape, Colin E; Drage, Trevor C; Cooper, Andrew I

    2014-06-25

    To impact carbon emissions, new materials for carbon capture must be inexpensive, robust, and able to adsorb CO2 specifically from a mixture of other gases. In particular, materials must be tolerant to the water vapor and to the acidic impurities that are present in gas streams produced by using fossil fuels to generate electricity. We show that a porous organic polymer has excellent CO2 capacity and high CO2 selectivity under conditions relevant to precombustion CO2 capture. Unlike polar adsorbents, such as zeolite 13x and the metal-organic framework, HKUST-1, the CO2 adsorption capacity for the hydrophobic polymer is hardly affected by the adsorption of water vapor. The polymer is even stable to boiling in concentrated acid for extended periods, a property that is matched by few microporous adsorbents. The polymer adsorbs CO2 in a different way from rigid materials by physical swelling, much as a sponge adsorbs water. This gives rise to a higher CO2 capacities and much better CO2 selectivity than for other water-tolerant, nonswellable frameworks, such as activated carbon and ZIF-8. The polymer has superior function as a selective gas adsorbent, even though its constituent monomers are very simple organic feedstocks, as would be required for materials preparation on the large industrial scales required for carbon capture. PMID:24874971

  20. Carbon dioxide and helium dissolved gases in groundwater at central Tenerife Island, Canary Islands: chemical and isotopic characterization

    NASA Astrophysics Data System (ADS)

    Marrero-Diaz, Rayco; López, Dina; Perez, Nemesio M.; Custodio, Emilio; Sumino, Hirochika; Melián, Gladys V.; Padrón, Eleazar; Hernandez, Pedro A.; Calvo, David; Barrancos, José; Padilla, Germán; Sortino, Francesco

    2015-10-01

    Seismic-volcanic unrest was detected between 2004 and 2005 in the central and northwest zones of Tenerife Island (Canary Islands, Spain). With the aim of strengthening the program of geochemical and seismic-volcanic surveillance, a study of the origin, characteristics, and spatial distribution of dissolved carbon dioxide (CO2) and helium (He) gases in the volcanic aquifer of central Tenerife Island and around Teide volcano was carried out. This work also improves the hydrogeological and hydrogeochemical conceptual model of groundwater flow. Dissolved CO2 concentrations in sampled groundwater are several orders of magnitude higher than that of air-saturated water (ASW) suggesting a significant contribution of non-atmospheric CO2, mainly magmatic, confirmed through measurement of isotopic compositions (δ13CTDIC) and total dissolved inorganic carbon (TDIC) concentrations. A vertical stratification of dissolved CO2 and δ13CTDIC values was observed in the volcanic aquifer at the eastern region of Las Cañadas Caldera. Stratification seems to be controlled by both degree of magmatic CO2-water interaction and CO2 degassing and the original δ13Cco2(g) isotopic composition. The highest dissolved helium (4He) concentrations in groundwater seem to be related to radiogenic contributions resulting from water-rock interactions, and increase with residence time, instead of with endogenous magmatic inputs. Isotopic systematics show that the dissolved gases in groundwater of central Tenerife are variable mixtures of CO2-3He-rich fluids of volcanic-hydrothermal origin with both organic and atmospheric components. The results suggest that the eastern area of Las Cañadas Caldera, the South Volcanic Ridge, and the Teide summit cone are the areas most affected by degassing of the volcanic-hydrothermal system, and they are therefore the most suitable zones for future geochemical monitoring.

  1. Evaluation of carbon dioxide mass transfer in raceway reactors for microalgae culture using flue gases.

    PubMed

    de Godos, I; Mendoza, J L; Acién, F G; Molina, E; Banks, C J; Heaven, S; Rogalla, F

    2014-02-01

    Mass transfer of CO2 from flue gas was quantified in a 100m(2) raceway. The carbonation sump was operated with and without a baffle at different liquid/gas ratios, with the latter having the greatest influence on CO2 recovery from the flue gas. A rate of mass transfer sufficient to meet the demands of an actively growing algal culture was best achieved by maintaining pH at ∼8. Full optimisation of the process required both pH control and selection of the best liquid/gas flow ratio. A carbon transfer rate of 10gCmin(-1) supporting an algal productivity of 17gm(-2)day(-1) was achieved with only 4% direct loss of CO2 in the sump. 66% of the carbon was incorporated into biomass, while 6% was lost by outgassing and the remainder as dissolved carbon in the liquid phase. Use of a sump baffle required additional power without significantly improving carbon mass transfer. PMID:24374031

  2. Control of mercury emissions in flue gases by activated carbon adsorption

    SciTech Connect

    Vidic, R.D.

    1996-12-31

    The adsorptive capacities of virgin and sulfur impregnated activated carbons (GAC) for gas-phase mercury were evaluated as a function of temperature and influent mercury concentration. The virgin activated carbon showed little adsorptive capacity, especially at temperatures above 90 {degrees}C. The pronounced effect of temperature on the adsorptive capacity evidences a physical adsorption mechanism between the mercury and virgin GAC. Sulfur impregnated activated carbons exhibited enhanced mercury removal efficiency over the non-impregnated varieties due to formation of mercuric sulfide on the carbon surface. This chemisorption process is enhanced with increased temperature between 25 and 90 {degrees}C. However, at 140 {degrees}C a decrease in adsorptive capacity occurs, indicating reduced formation of mercuric sulfide. The method used for impregnating GAC with sulfur had a pronounced effect on mercury removal capacity. The chemical bonding of sulfur and carbon surface at 600 {degrees}C provides a more uniform distribution of sulfur throughout the GAC pore structure than achieved by conventional condensation techniques, yielding improved performance.

  3. The Path of Carbon in Photosynthesis II. Amino Acids

    DOE R&D Accomplishments Database

    Stepka, W.; Benson, A. A.; Calvin, M.

    1948-05-25

    The radioactive amino acid's synthesized from C{sup 14}O{sub 2} by green algae both in the light and in the dark after CO{sub 2}-free preillumination have been separated and identified using paper chromatography and radioautography. The radioactive amino acids identified were aspartic acid, alanine and smaller amounts of 3- and 4-carbon amino acids. This finding as well as the total absence of radioactive glutamic acid substantiates the mechanism for reduction of CO{sub 2} previously postulated by members of this laboratory.

  4. On the potential of long carbon nanotube forest for sensing gases and vapors

    NASA Astrophysics Data System (ADS)

    Khavrus, Vyacheslav O.; Vinzelberg, Hartmut; Schumann, Joachim; Leonhardt, Albrecht; Oswald, Steffen; Bchner, Bernd

    2011-04-01

    Ensembles of contacting carbon nanotubes (CNTs) undergo changes of electrical resistance at exposition to an ambient gas atmosphere due to the sensitivity of their electronic structure to adsorbed molecules. This phenomenon has been studied in dependence on temperature, the purity of carrier gas and operational history using a sensor-like device prepared by means of a vertically aligned multi-walled CNT forest. The CNT ensemble was grown by aerosol-assisted chemical vapor deposition using a ferrocene-acetonitrile solution. The sensitivity to O 2, CO 2, NH 3, CH 4 and C 2H 4 was measured at different temperatures. The presented study allows the conclusion that the high sensitivity of the carbon surface to changes of temperature, vaporized water and oxygen present in the air or to contaminations of the carrier gas decreases the potential of carbon-based devices for practical sensing applications. A possible mechanism of working of CNT-based sensing devices is discussed.

  5. Characterization of carbon black modified by maleic acid

    NASA Astrophysics Data System (ADS)

    Asokan, Vijayshankar; Kosinski, Pawel; Skodvin, Tore; Myrseth, Velaug

    2013-09-01

    We present here a method for modifying the surface of carbon black (CB) using a simple heat treatment in the presence of a carboxylic acid as well as water or ethylene glycol as a solvent. CB was mixed with maleic acid and either water or ethylene glycol, and heated at 250C. Unlike the traditional surface modification processes which use heat treatment of carbon with mineral acids the present modification method using a carboxylic acid proved to be simple and time efficient. CB from two different vendors was used, and the modified samples were characterized by TGA, BET surface area measurement, XRD, particle size and zeta potential measurements, and FTIR. It was found that several material properties, including thermal stability and surface area, of the modified CB are significantly altered relative to the parental carbon samples. This method provides a rapid and simple route to tailor new materials with desired properties.

  6. Shock-tube thermochemistry tables for high-temperature gases. Volume 5: Carbon dioxide

    NASA Technical Reports Server (NTRS)

    Menard, W. A.; Horton, T. E.

    1971-01-01

    Equilibrium thermodynamic properties and species concentrations for carbon dioxide are tabulated for moving, standing, and reflected shock waves. Initial pressures range from 6.665 to 6665 N/sq m (0.05 to 50.0 torr), and temperatures from 2,000 to over 80,000K. In this study, 20 molecular and atomic species were considered.

  7. A Pilot-Scale Evaluation of a New Technology to Control NO(x) Emissions from Boilers at KSC: Hydrogen Peroxide Injection into Boiler Flue Gases Followed by Wet Scrubbing of Acid Gases

    NASA Technical Reports Server (NTRS)

    Cooper, C. David

    1997-01-01

    Emissions of nitrogen oxides NO(x) are a significant problem in the United States. NO(x) are formed in any combustion process, therefore it is not surprising that NO(x) are emitted from the boilers at KSC. Research at UCF has shown (in the laboratory) that injecting H2O2 into hot simulated flue gases can oxidize the NO and NO2 to their acid gas forms, HNO2 and HNO3, respectively. These acid gases are much more water soluble than their counterparts, and theoretically can be removed easily by wet scrubbing. This technology was of interest to NASA, both for their boilers at KSC, and for their combustion sources elsewhere. However, it was necessary to field test the technology and to provide pilot-scale data to aid in design of full-scale facilities. Hence this project was initiated in May of 1996.

  8. Regiocontrolled intramolecular cyclizations of carboxylic acids to carbon-carbon triple bonds promoted by acid or base catalyst.

    PubMed

    Uchiyama, Masanobu; Ozawa, Hiroki; Takuma, Kazuya; Matsumoto, Yotaro; Yonehara, Mitsuhiro; Hiroya, Kou; Sakamoto, Takao

    2006-11-23

    We systematically investigated, for the first time, the relationship between regioselectivity and acid/base effects in the cyclization reactions between carboxylic acids and carbon-carbon triple bonds. We found novel acid- and base-promoted cyclizations to selectively give isocoumarin or pyran-2(2H)-one and phthalide or furan-2(5H)-one skeletons, respectively, and established a catalytic version of regioselective heterocyclic ring synthesis. Density functional theory calculations and application to a short route to thunberginol A were also described. [reaction: see text]. PMID:17107061

  9. Self-recovering soot detector, particularly to monitor carbon content in diesel engine exhaust gases

    SciTech Connect

    Sarholz, W.

    1981-12-22

    An insulating support body, for example an aluminum oxide ceramic, supports two electrodes spaced from each other by a small gap, for example 0.1 mm, which will have therebetween a high resistance. Upon collection of soot, the resistance between the electrodes across the gap will drop, which can be indicated by sensing current through the electrodes upon connection to a source of electrical energy. To remove soot upon termination of smoking, or soot contents in the gases, the electrodes are applied over, or embedded in a layer of essentially nonconducting catalyzing material which, in the presence of oxygen, catalyzes the oxidation of soot located in the gap between the electrodes to thereby remove the soot by oxidation and restore the resistance of the path between the electrodes and hence the sensitivity of the sensor for subsequent detection of accumulation of soot in the gap. Preferably, the non-conductive catalyzing material is a mixture of platinum, or a platinum metal , or a platinum metal alloy and a metal oxide which is compatible with, or identical to the ceramic base, for example aluminum oxide. The essentially electrically non-conductive layer can be applied by thick-film technology, and the electrodes also by thick-film technology thereover, or the electrodes may be in the form of fine platinum wires extending through the catalyzing electrically non-conductive layer. The sensing element can be held in a housing or socket, similar to a spark plug socket.

  10. Functionalization of Single Wall Carbon Nanotubes with Carboxylic Acids

    NASA Astrophysics Data System (ADS)

    Viswanathan, Sriram; Britt, Phillip F.; Ivanov, Ilia N.; Puretzky, Alex A.; Lance, Michael J.; Geohegan, David B.; Oak Ridge National Laboratory Collaboration

    2003-03-01

    The chemical functionalization of single-wall carbon nanotubes (SWNT) is necessary to solubilize the materials and to assist in the dispersion of the bundles for a variety of applications. One approach has been to derivatize the pendant carboxyl groups that are formed in the oxidative purification of the SWNT. Unfortunately, these carboxyl groups are found in low concentrations because the purification conditions also leads to decarboxylation. Thus, methods were investigated to increase the concentration of carboxylic acids on SWNT by chemical oxidation with a variety of reagents including potassium permanganate, sulfuric acid/nitric acid, and sulfuric acid/hydrogen peroxide. The concentration of carboxylic acids was analyzed by FTIR, and the samples were characterized by TGA, Raman spectroscopy, SEM, and TEM. Surprisingly, many of the oxidative methods lead to the formation of amorphous carbon and little if any increase in carboxyl content of the SWNT.

  11. Effects of Gases on Field Emission from Single and Multi-Wall Carbon Nanotubes

    NASA Astrophysics Data System (ADS)

    Wadhawan, A.; Stephens, K.; Stallcup, R., II; Perez, J.; Physics Department Collaboration

    2001-03-01

    We report the effects of O_2, H_2, and Ar exposure on the field emission properties of single and multi-wall carbon nanotubes. The field emission current vs. voltage curves and field emission current vs. time were measured as a function of gas exposure at 10-8 Torr over a period of approximately 8 hours. The data were collected using an automated system running under Labview. We find that H2 and Ar exposure do not significantly affect the field emission properties of either single or multi-walled carbon nanotubes. However, O2 exposure degrades the field emission properties of multi-wall tubes more than those of single-wall tubes. After O2 exposure, the turn-on voltage for multi-wall tubes increased fromm 300 to 500 volts, while the turn-on voltage for single-wall tubes increased from 200 to 250 volts. An explanation of these results will be discussed.

  12. Fragrance material review on carbonic acid, methyl phenylmethyl ester.

    PubMed

    McGinty, D; Letizia, C S; Api, A M

    2012-09-01

    A toxicologic and dermatologic review of carbonic acid, methyl phenylmethyl ester when used as a fragrance ingredient is presented. Carbonic acid, methyl phenylmethyl ester is a member of the fragrance structural group Aryl Alkyl Alcohol Simple Acid Esters (AAASAE). The AAASAE fragrance ingredients are prepared by reacting an aryl alkyl alcohol with a simple carboxylic acid (a chain of 1-4 carbons) to generate formate, acetate, propionate, butyrate, isobutyrate and carbonate esters. This review contains a detailed summary of all available toxicology and dermatology papers that are related to this individual fragrance ingredient and is not intended as a stand-alone document. Available data for carbonic acid, methyl phenylmethyl ester were evaluated, then summarized, and includes: physical properties, acute toxicity, skin irritation, and skin sensitization data. A safety assessment of the entire AAASAE will be published simultaneously with this document. Please refer to Belsito et al. (2012) for an overall assessment of the safe use of this material and all AAASAE in fragrances. PMID:22414647

  13. Characterization of the flow of the CO/CO 2 gases through carbon nanotube junctions using molecular dynamic simulations

    NASA Astrophysics Data System (ADS)

    Sabzyan, Hassan; Tavangar, Zahra

    2009-08-01

    A detailed study of the gas flow in carbon nanotubes (CNT) and carbon nanotube junctions (CNTJ) can open the way towards the study of the reaction mixture flow in prospective nano-reactors. In this work, flow of the pure and mixed CO/CO 2 gases through some selected CNTs and three types of CNT1- J-CNT2 CNTJs, ( 12, 12)- J-( 3, 8), ( 12, 8)- J-( 8, 12) and ( 8, 8)- J-( 13, 0), are studied using molecular dynamic simulations. Results of this study show that regardless of the diameter and helicity type of the CNT1 and CNT2, when the flow starts with the molecules in the CNT1, the number density of molecules in the CNT2 is higher than that in the CNT1. Projected radial distribution of the molecules are calculated and analyzed in terms of the molecule-molecule and molecule-wall interactions. The well-structured projected radial distribution results show that the CNT radius and helicity as well as the type of molecules determine the lateral distribution of the gas molecules along the flow.

  14. Greenhouse Gases

    MedlinePLUS

    ... and the Environment Greenhouse Gases Effect on the Climate Where Greenhouse Gases Come From Outlook for Future ... effects. More about how greenhouse gases affect the climate » Also on Energy Explained Energy and the Environment ...

  15. Enhancement of acidic gases in biomass burning impacted air masses over Canada

    NASA Technical Reports Server (NTRS)

    Lefer, B. L.; Talbot, R. W.; Harriss, R. C.; Bradshaw, J. D.; Sandholm, S. T.; Olson, J. O.; Sachse, G. W.; Collins, J.; Shipham, M. A.; Blake, D. R.

    1994-01-01

    Biomass-burning impacted air masses sampled over central and eastern Canada during the summer of 1990 as part of ABLE 3B contained enhanced mixing ratios of gaseous HNO3, HCOOH, CH3COOH, and what appears to be (COOH)2. These aircraft-based samples were collected from a variety of fresh burning plumes and more aged haze layers from different source regions. Values of the enhancement factor, delta X/delta CO, where X represents an acidic gas, for combustion-impacted air masses sampled both near and farther away from the fires, were relatively uniform. However, comparison of carboxylic acid emission ratios measured in laboratory fires to field plume enhancement factors indicates significant in-plume production of HCOOH. Biomass-burning appears to be an important source of HNO3, HCOOH, and CH3COOH to the troposphere over subarctic Canada.

  16. Sulfuric acid vapor and other cloud-related gases in the Venus atmosphere - Abundances inferred from observed radio opacity

    NASA Technical Reports Server (NTRS)

    Steffes, P. G.; Eshleman, V. R.

    1982-01-01

    It is suggested that the absorbing characteristics of sulfuric acid vapor appear to reconcile what had been thought to be an inconsistency among measurements and deductions regarding the constituents of the Venus atmosphere and radio occultation, radar reflection, and radio emission measurements of its opacity. Laboratory measurements of sulfuric acid, sulfur dioxide, water vapor, and carbon dioxide are used to model relative contributions to opacity as a function of height in a way that is consistent with observations of the constituents and absorbing properties of the atmosphere. It is concluded that sulfuric acid vapor is likely to be the principal microwave absorber in the 30-50 km altitude range of the middle atmosphere of Venus.

  17. Studies of the Terrestrial Molecular Oxygen and Carbon Cycles in Sand Dune Gases and in Biosphere 2.

    NASA Astrophysics Data System (ADS)

    Severinghaus, Jeffrey Peck

    Molecular oxygen in the atmosphere is coupled tightly to the terrestrial carbon cycle by the processes of photosynthesis, respiration, and burning. This dissertation examines different aspects of this coupling in four chapters. Chapter 1 explores the feasibility of using air from sand dunes to reconstruct atmospheric O_2 composition centuries ago. Such a record would reveal changes in the mass of the terrestrial biosphere, after correction for known fossil fuel combustion, and constrain the fate of anthropogenic CO_2. Test drilling in sand dunes shows that sand dunes do contain old air, as shown by the concentrations of chlorofluorocarbons and ^{85}Kr. Diffusion is shown to dominate mixing rather than advection. However, biological respiration in dunes corrupts the signal, and isotopic analysis of O_2 and N _2 shows that fractionation of the gases precludes use of sand dunes as archives. Chapter 2 further explores this fractionation, revealing a previously unknown "water vapor flux fractionation" process. A flux of water vapor out of the moist dune into the dry desert air sweeps out the other gases, forcing them to diffuse back into the dune. The heavy isotopes of N_2 and O_2 diffuse more slowly, creating a steady state depletion of heavy isotopes in the dune interior. Molecular diffusion theory and a laboratory simulation of the effect agree well with the observations. Additional fractionation of the dune air occurs via thermal diffusion and gravitational settling, and it is predicted that soil gases in general will enjoy all three effects. Chapter 3 examines the cause of a mysterious drop in O _2 concentrations in the closed ecosystem of Biosphere 2, located near Tucson, Arizona. The organic -rich soil manufactured for the experiment is shown to be the culprit, with CO_2 produced by bacterial respiration of the organic matter reacting with the extensive concrete surfaces inside. Chapter 4 examines the O_2:C stoichiometry of terrestrial soil respiration and photosynthesis, in the context of using atmospheric O_2 measurements to constrain the size of the "missing sink" of CO_2. Direct measurements of soil respiration and biomatter elemental abundance suggest a value of 1.1 +/- 0.05 oxygen molecules per CO_2 molecule.

  18. Separation of polar gases from nonpolar gases

    DOEpatents

    Kulprathipanja, Santi; Kulkarni, Sudhir S.

    1986-01-01

    Polar gases such as hydrogen sulfide, sulfur dioxide and ammonia may be separated from nonpolar gases such as methane, nitrogen, hydrogen or carbon dioxide by passing a mixture of polar and nonpolar gases over the face of a multicomponent membrane at separation conditions. The multicomponent membrane which is used to effect the separation will comprise a mixture of a glycol plasticizer having a molecular weight of from about 200 to about 600 and an organic polymer cast on a porous support. The use of such membranes as exemplified by polyethylene glycol and silicon rubber composited on polysulfone will permit greater selectivity accompanied by a high flux rate in the separation process.

  19. Separation of polar gases from nonpolar gases

    DOEpatents

    Kulprathipanja, S.; Kulkarni, S.S.

    1986-08-26

    Polar gases such as hydrogen sulfide, sulfur dioxide and ammonia may be separated from nonpolar gases such as methane, nitrogen, hydrogen or carbon dioxide by passing a mixture of polar and nonpolar gases over the face of a multicomponent membrane at separation conditions. The multicomponent membrane which is used to effect the separation will comprise a mixture of a glycol plasticizer having a molecular weight of from about 200 to about 600 and an organic polymer cast on a porous support. The use of such membranes as exemplified by polyethylene glycol and silicon rubber composited on polysulfone will permit greater selectivity accompanied by a high flux rate in the separation process.

  20. USE OF FATTY ACID STABLE CARBON ISOTOPE RATIO TO INDICATE MICROBIAL CARBON SOURCE IN TROPICAL SOILS

    EPA Science Inventory


    We use measurements of the concentration and stable carbon isotope ratio of individual microbial phospholipid fatty acids (PLFAs) in soils as indicators of live microbial biomass levels, broad microbial community structure, and microbial carbon source. For studies of soil o...

  1. Photosynthesis In Elodea canadensis Michx: Four-Carbon Acid Synthesis.

    PubMed

    Degroote, D; Kennedy, R A

    1977-06-01

    Experiments to determine the early labeled photosynthetic products in Elodea canadensis show that after 2 seconds of exposure to NaH(14)CO(3), 45% of the (14)C incorporated is located in malate and aspartate. Phosphoglyceric acid and sugars account for 27% of the label during similar exposures. Equivalent amounts of organic acids and C(3) cycle products are present after 8 seconds. Four-carbon acids remain relatively unchanged throughout the first 45 seconds of exposure, while sugars increase in a linear fashion. Enzyme assays indicate that ribulose diphosphate and phosphoenolpyruvate carboxylase enzymes are present in a ratio of approximately 2:1. It appears that E. canadensis is able to synthesize significant amounts of four-carbon acids via beta-carboxylation and this may play a role in maintaining a pH favorable for carboxylation in aquatic plants. PMID:16660008

  2. Laboratory simulation of meteoritic noble gases. II - Sorption of xenon on carbon: Etching and heating experiments

    NASA Technical Reports Server (NTRS)

    Zadnik, M. G.; Wacker, J. F.; Lewis, R. S.

    1985-01-01

    The release of trapped Xe from amorphous-C phases of meteorites is simulated experimentally by HNO3 etching of carbon-black and pyrolyzed polyvinylidene chloride samples exposed to Xe-127 for 0.5-240 h at 100-1000 C and then degassed for 9 h or more at the same temperatures, as reported by Wacker et al. (1985). The results are presented in tables and graphs and characterized in detail. Samples exposed at 100-200 C are found to lose most of their Xe after etching to a depth of only about 20 pm, while those exposed at 800-1000 C exhibit a second more tightly bound component extending to a depth of 3 nm, indicative of diffusion of Xe during exposure and resembling planetary Xe. The higher noble-gas concentrations measured in meteorites are attributed to rate-controlled Xe uptake over a long period in the solar nebula.

  3. Laboratory simulation of meteoritic noble gases. II - Sorption of xenon on carbon: Etching and heating experiments

    NASA Astrophysics Data System (ADS)

    Zadnik, M. G.; Wacker, J. F.; Lewis, R. S.

    1985-04-01

    The release of trapped Xe from amorphous-C phases of meteorites is simulated experimentally by HNO3 etching of carbon-black and pyrolyzed polyvinylidene chloride samples exposed to Xe-127 for 0.5-240 h at 100-1000 C and then degassed for 9 h or more at the same temperatures, as reported by Wacker et al. (1985). The results are presented in tables and graphs and characterized in detail. Samples exposed at 100-200 C are found to lose most of their Xe after etching to a depth of only about 20 pm, while those exposed at 800-1000 C exhibit a second more tightly bound component extending to a depth of 3 nm, indicative of diffusion of Xe during exposure and resembling planetary Xe. The higher noble-gas concentrations measured in meteorites are attributed to rate-controlled Xe uptake over a long period in the solar nebula.

  4. Carbon and nitrogen dynamics and greenhouse gases emissions in constructed wetlands: a review

    NASA Astrophysics Data System (ADS)

    Jahangir, M. M. R.; Fenton, O.; Gill, L.; Müller, C.; Johnston, P.; Richards, K. G.

    2014-07-01

    The nitrogen (N) removal efficiency of constructed wetlands (CWs) is very inconsistent and does not alone explain if the removed species are reduced by physical attenuation or if they are transformed to other reactive forms (pollution swapping). There are many pathways for the removed N to remain in the system: accumulation in the sediments, leaching to groundwater (nitrate-NO3- and ammonium-NH4+), emission to atmosphere via nitrous oxide- N2O and ammonia and/or conversion to N2 gas and adsorption to sediments. The kinetics of these pathways/processes varies with CWs management and therefore needs to be studied quantitatively for the sustainable use of CWs. For example, the quality of groundwater underlying CWs with regards to the reactive N (Nr) species is largely unknown. Equally, there is a dearth of information on the extent of Nr accumulation in soils and discharge to surface waters and air. Moreover, CWs are rich in dissolved organic carbon (DOC) and produce substantial amounts of CO2 and CH4. These dissolved carbon (C) species drain out to ground and surface waters and emit to the atmosphere. The dynamics of dissolved N2O, CO2 and CH4 in CWs is a key "missing piece" in our understanding of global greenhouse gas budgets. In this review we provide an overview of the current knowledge and discussion about the dynamics of C and N in CWs and their likely impacts on aquatic and atmospheric environments. We suggest that the fate of various N species in CWs and their surface emissions and subsurface drainage fluxes need to be evaluated in a holistic way to better understand their potential for pollution swapping. Research on the process based N removal and balancing the end products into reactive and benign forms are critical to assess environmental impacts of CWs. Thus we strongly suggest that in situ N transformation and fate of the transformation products with regards to pollution swapping requires further detailed examination.

  5. A mechanistic model of wormhole growth in carbonate matrix acidizing and acid fracturing

    SciTech Connect

    Hung, K.M.; Hill, A.D.; Sepehrnoorl, K.

    1989-01-01

    A mathematical model that describes the growth and competition of wormholes during ann acidizing treatment in a carbonate formation was developed. The model is initialized with the distribution of largest pores. Wormhole characteristics (size, length, and distribution) were found too be controlled by acid-injection, diffusion, and fluid-loss rates.

  6. Anaerobic carbon metabolism by the tricarboxylic acid cycle

    SciTech Connect

    Vanlerberghe, G.C.; Horsey, A.K.; Weger, H.G.; Turpin, D.H. )

    1989-12-01

    Nitrogen-limited cells of Selenastrum minutum (Naeg.) Collins are able to assimilate NH{sub 4}{sup +} in the dark under anaerobic conditions. Addition of NH{sub 4}{sup +} to anaerobic cells results in a threefold increase in tricarboxylic acid cycle (TCAC) CO{sub 2} efflux and an eightfold increase in the rate of anaplerotic carbon fixation via phosphoenspyruvate carboxylase. Both of these observations are consistent with increased TCAC carbon flow to supply intermediates for amino acid biosynthesis. Addition of H{sup 14}CO{sub 3}{sup {minus}} to anaerobic cells assimilating NH{sub 4}{sup +} results in the incorporation of radiolabel into the {alpha}-carboxyl carbon of glutamic acid. Incorporation of radiolabel into glutamic acid is not simply a short-term phenomenon following NH{sub 4}{sup +} addition as the specific activity of glutamic acid increases over time. This indicates that this alga is able to maintain partial oxidative TCAC carbon flow while under anoxia to supply {alpha}ketoglutarate for glutamate production. During dark aerobic NH{sub 4}{sup +} assimilation, no radiolabel appears in fumarate or succinate and only a small amount occurs in malate. During anaerobic NH{sub 4}{sup +} assimilation, these metabolites contain a large proportion of the total radiolabel and radiolabel accumulates in succinate over time. Also, the ratio of dark carbon fixation to NH{sub 4}{sup +} assimilation is much higher under anaerobic than aerobic conditions. These observations suggest the operation of a partial reductive TCAC from oxaloacetic acid to malate, fumarate, and succinate. Such a pathway might contribute to redox balance in an anaerobic cell maintaining partial oxidative TCAC activity.

  7. Robust IR Remote Sensing Technique of the Total Column of Trace Gases Including Carbon Dioxide and Methane

    NASA Technical Reports Server (NTRS)

    Georgieva, E. M.; Heaps, W. S.

    2011-01-01

    Progress on the development of a differential radiometer based upon the Fabry-Perot interferometer (FPI) for methane (CH4) and carbon dioxide (C02) detection in the atmosphere is presented. Methane measurements are becoming increasingly important as a component of NASA's programs to understand the global carbon cycle and quantifY the threat of global warming. Methane is the third most important greenhouse gas in the Earth's radiation budget (after water vapor and carbon dioxide) and the second most important anthropogenic contributor to global warming. The importance of global warming and air quality to society caused the National Research Council to recommend that NASA develop the following missions [1]: ASCENDS (Active Sensing of C02 Emissions over Nights, Days, and Seasons), GEOCAPE (Geostationary Coastal and Air Pollution Events), and GACM (Global Atmosphere Composition Mission). Though methane measurements are not specifically called out in these missions, ongoing environmental changes have raised the importance of understanding the methane budget. In the decadal survey is stated that "to close the carbon budget, we would also address methane, but the required technology is not obvious at this time. If appropriate and cost-effective methane technology becomes available, we strongly recommend adding a methane capability". In its 2007 report the International Panel on Climate Change identified methane as a key uncertainty in our understanding saying that the causes of recent changes in the growth rate of atmospheric CH4 are not well understood. What we do know is that methane arises from a number of natural sources including wet lands and the oceans plus man made sources from agriculture, as well as coal and petroleum production and distribution. It has recently been pointed out that large amount of methane are frozen in the permafrost of Canada and Siberia. There is a fear that melting of this permafrost driven by global warming may release large amounts of methane very suddenly further exacerbating climate change [2]. Last year our group began a joint effort with Johns Hopkins Applied Physics Laboratory to investigate the possibility of developing a small unmanned aerial vehicle (UAV) equipped to measure greenhouse gases-particularly methane. Although we are targeting our system for smaller UAV's the instrument will be directly applicable to missions involving larger NASA UAV's such as Global Hawk or even on missions utilizing manned aircraft. Because of its small size, inherent ruggedness and simplicity some version of our proposed instrument may find a role as a satellite instrument for NASA or NOAA.

  8. Quantum cascade laser absorption sensor for carbon monoxide in high-pressure gases using wavelength modulation spectroscopy.

    PubMed

    Spearrin, R M; Goldenstein, C S; Jeffries, J B; Hanson, R K

    2014-03-20

    A tunable quantum cascade laser sensor, based on wavelength modulation absorption spectroscopy near 4.8 μm, was developed to measure CO concentration in harsh, high-pressure combustion gases. The sensor employs a normalized second harmonic detection technique (WMS-2f/1f) at a modulation frequency of 50 kHz. Wavelength selection at 2059.91  cm⁻¹ targets the P(20) transition within the fundamental vibrational band of CO, chosen for absorption strength and relative isolation from infrared water and carbon dioxide absorption. The CO spectral model is defined by the Voigt line-shape function, and key line-strength and line-broadening spectroscopic parameters were taken from the literature or measured. Sensitivity analysis identified the CO-N₂ collisional broadening coefficient as most critical for uncertainty mitigation in hydrocarbon/air combustion exhaust measurements, and this parameter was experimentally derived over a range of combustion temperatures (1100-2600 K) produced in a shock tube. Accuracy of the wavelength-modulation-spectroscopy-based sensor, using the refined spectral model, was validated at pressures greater than 40 atm in nonreactive shock-heated gas mixtures. The laser was then free-space coupled to an indium-fluoride single-mode fiber for remote light delivery. The fiber-coupled sensor was demonstrated on an ethylene/air pulse detonation combustor, providing time-resolved (~20  kHz), in situ measurements of CO concentration in a harsh flow field. PMID:24663473

  9. Interactions of gases in molten salts: Carbon dioxide and oxygen in cryolite alumina melts

    NASA Astrophysics Data System (ADS)

    Numata, H.; Bockris, J. O'm.

    1984-01-01

    A radiotracer method has been developed to measure the solubility of CO2 in cryolite-based systems at temperatures above 1273 K and also a method to measure the solubility of oxygen. The high solubility of CO2 in cryolite (0.34 pct A12O3, 1.68 pct CaF2), and the highly negative AH of solution, suggest complex formation. In the presence of 5.33 pct excess A12O3, the solubility of CO2 is several times greater than in cryolite. In contrast, oxygen shows a solubility about a thousandth that of CO2. The entropy of CO2 in cryolite indicates a loss of translational degrees of freedom in a manner consistent with complexing. However, in the presence of increased A12O3 (in spite of the increase of solubility) the entropy change upon solution appears to indicate little loss of translational freedom. It is suggested that CO2 is complexed in both systems, but more strongly in the cryolite system. Complexing in cryolite produces the small carbonate (CO- 3)ion, and this compensates the loss of translational freedom arising from the CO2 complexing with aluminofluorides. Measured solubilities for CO2 were 1.0 X 10-3 moles liter-1 atm-1 in cryolite at 1273 K, 4.6 x 10-3 moles liter-1 atm-1 in (NaF)2:3 A1F3 + 5.33 wt pct A12O3 at 1233 K. At 1230 K, oxygen showed a solubility of only 3.0 X 106 moles liter-1 atm-1 in the latter melt.

  10. Sequential Mukaiyama-Michael reaction induced by carbon acids.

    PubMed

    Yanai, Hikaru; Kobayashi, Osamu; Takada, Kenji; Isono, Takuya; Satoh, Toshifumi; Matsumoto, Takashi

    2016-02-16

    In the presence of a strong carbon acid, the sequential Mukaiyama-Michael reaction using two different Michael acceptors proceeded and the reaction of ketene silyl acetal derived from EtOAc with α-pyrones as primal acceptors yielded the corresponding cyclic ketene silyl acetals, which were reactive enough to undergo the following reaction with second acceptors. PMID:26734829

  11. ELEMENTAL MERCURY ADSORPTION BY ACTIVATED CARBON TREATED WITH SULFURIC ACID

    EPA Science Inventory

    The paper gives results of a study of the adsorption of elemental mercury at 125 C by a sulfuric-acid (H2S04, 50% w/w/ solution)-treated carbon for the removal of mercury from flue gas. The pore structure of the sample was characterized by nitrogen (N2) at -196 C and the t-plot m...

  12. Actions and interactions of nitric oxide, carbon monoxide and hydrogen sulphide in the cardiovascular system and in inflammation--a tale of three gases!

    PubMed

    Li, Ling; Hsu, Anna; Moore, Philip K

    2009-09-01

    Nitric oxide (NO), carbon monoxide (CO) and hydrogen sulphide (H(2)S) together make up a family of biologically active gases (the so-called 'gaseous triumvirate') with an increasingly well defined range of physiological effects plus roles to play in a number of disease states. Over the years, most researchers have concentrated their attention on understanding the part played by a single gas in one or more body systems. It is becoming more clear that all three gases are synthesised naturally in the body, often by the same cells within the same organs, and that all three gases exert essentially similar biological effects albeit via different mechanisms. Within the cardiovascular system, for example, all are vasodilators, promote angiogenesis and vascular remodelling and are protective towards tissue damage in for example, ischaemia-reperfusion injury in the heart. Similarly, all exhibit complex effects in inflammation with both pro- and anti-inflammatory effects recognised. It seems likely that cell function is controlled not by the activity of single gases working in isolation but by the concerted activity of all three of these gases working together. PMID:19486912

  13. Acid dew and the role of chemistry in the dry deposition of reactive gases to wetted surfaces

    NASA Technical Reports Server (NTRS)

    Chameides, William L.

    1987-01-01

    A formalism is developed to describe the dry deposition of soluble reactive gases to wetted surfaces in terms of the relevant meteorological conditions, the surface roughness, the total amount of liquid water present on the surface, the rate of accumulation of this water, and the species' solubility and reactivity in the surface water. This formulation is then incorporated into a model designed to simulate the generation of acidic dew from the deposition of HNO3, SO2, S(IV) oxidants, H2O2, and O3. Similar to the observations of dew in the continental U.S., the model generates a dewdrop pH of about 4 by the end of the night; the pH can rapidly fall to toxic levels due to rapid evaporation after sunrise. Relatively low deposition velocities are predicted for the SO2 and O3 because of their lower solubilities and hence larger surface resistances than those of the other oxidants. Because the chemical lifetime of the SO2 in the dew is influenced by the atmospheric levels of H2O2, O3, and SO2, the SO2 deposition velocity is a strong function of these species' atmospheric abundances.

  14. Abundance and isotope systematics of carbon in subglacial basalts, geothermal gases and fluids from Iceland's rift zones

    NASA Astrophysics Data System (ADS)

    Barry, P. H.; Hilton, D. R.; Fueri, E.; Halldorsson, S. A.; Fischer, T. P.; Gronvold, K.

    2010-12-01

    P. H. BARRY1*, D. R. HILTON1, E. FÜRI1, S.A. HALLDÓRSON1, T.P. FISCHER2, K. GRONVOLD3 1 Scripps Institution of Oceanography, UCSD, La Jolla, California 92093, USA (*Correspondence: pbarry@ucsd.edu). 2University of New Mexico, Albuquerque, NM 87131, USA. 3University of Iceland, Askja, Sturlugata 7, IS-101, Reykjavik, Iceland Carbon dioxide (CO2) is the dominant non-aqueous volatile species found in oceanic basalts and geothermal fluids and serves as the carrier gas for trace volatiles such as He and other noble gases. The aim of this study is to identify the superimposed effects of degassing and crustal contamination on the CO2 systematics of the Icelandic hotspot in order to reveal and characterize the carbon abundance and isotopic features of the underlying mantle source. Our approach involves coupling CO2 with He, utilizing the sensitivity of 3He/4He ratios to reveal mantle and crustal inputs. We report new C-isotope (δ13C) and abundance characteristics for a suite of 47 subglacial basalts and 50 geothermal gases and fluids from Iceland. CO2 contents in hyaloclastite glasses are extremely low (10-100 ppm) and likely residual following extensive degassing whereas geothermal fluids are dominated by CO2 (>90 %). C-isotopes range from -27.2 to -3.6 ‰ (vs. PDB) for basalts and from -18.8 to 2.86 ‰ (vs. PDB) for geothermal samples (mean = -4.2 ± 3.6 ‰). CO2/3He ratios range from 108 to 1012 for basalts and from 105 to 1012 for geothermal samples: In both cases, our results extend He-CO2 relationships over a much broader range than reported previously [1]. Taken together, these data suggest that several processes including mixing, degassing, and/or syn- or post-eruptive crustal contamination may act to modify CO2 source characteristics. Equilibrium degassing models are compatible with ~75 % of the basalt data, and preliminary results indicate that initial Icelandic source characteristics are ~500 ppm CO2 and δ13C ~ -5 ‰ (vs. PDB). These values are high compared to N-MORB mantle source estimates (72-134 ppm) based upon CO2/Nb ratios [2, 3]; however, they are in good agreement with those from submarine glasses on adjacent segments from the Reykjanes and Kolbeinsey ridges [4,5]. Significantly, the model-derived δ13C estimate is close to the mean Icelandic geothermal value, implying that fluids closely resemble source values, i.e. they likely represent the exsolved component. Integrating the estimated source CO2 content with magma production values of 0.079 km3/yr [6] yields a CO2 flux of ~1.2 x 1011 mol CO2 yr-1for Iceland, representing ~ 5.4 % of the total carbon ridge flux of 2.2 x 1012 mol CO2 yr-1 [7]. Thus, the average CO2 flux estimate for Iceland is ~2.2 x 108 mol CO2 yr-1km-1 strike of ridge axis, which compares to an overall ridge flux (including Iceland) of ~2.9 x 107 mol CO2 yr-1km-1. This difference highlights both heterogeneity in source volatile contents and magma production rates as important controls for determining mantle CO2 fluxes. [1] Poreda et al., 1992 [2] Saal et al., 2002. [3] Shaw et al., 2010. [4] de Leeuw, 2007 [5] Macpherson et al., 2005. [6] Thordarson et al., 2007 [7] Marty et al., 1998.

  15. Helium and carbon isotope systematics of Rungwe geothermal gases and fluids; southern Tanzania

    NASA Astrophysics Data System (ADS)

    Barry, P. H.

    2009-12-01

    P. H. BARRY1*, D. R. HILTON1, T. P. FISCHER2, J. M. DE MOOR2, F. MANGASINI3 C. RAMIREZ4 1 Geosciences Research Division, Scripps Institution of Oceanography, UCSD, La Jolla, California 92093-0244, USA (*Correspondence: pbarry@ucsd.edu) 2 Department of Earth and Planetary Sciences, MSC 03 2040, 1 University of New Mexico, Albuquerque, New Mexico 87131-0001, USA. 3 Department of Mining and Mineral Processing Engineering, University of Dar Es Salaam, PO Box 35131, Dar Es Salaam, Tanzania. 4 Centro de Investigaciones en Ciencias Geologicas, Escuela Centroamericana de Geologia, Universidad de Costa Rica. The East African Rift (EAR) is the largest modern example of continental rifting, extending from the Afar depression in the north to the Rungwe region in southern Tanzania. EAR volcanism is attributed to the presence of one or more mantle plumes [1]. Late Miocene to recent volcanism and geothermal activity mark the Rungwe region [2], with mafic eruptions as recently as 200 years ago. Our aim is to delineate the southern geographical extent of plume influence on the propagating EAR by investigating the He-CO2 characteristics of geothermal fluids in the Rungwe region. We report new helium (He) and carbon (C) isotopes (3He/4He, δ13C) and relative abundance (CO2/3He) characteristics for a suite of 20 geothermal gas and fluid samples from 11 different localities in the Rungwe region. He-isotopes are in good agreement with previous reports [3], and range from ~1 RA to ~7 RA (MORB-like values), indicating admixture between upper mantle He and variable proportions of radiogenic He. C-isotopes ranges from -2.8 to -6.5 ‰ (vs. PDB) with all falling in the MORB range (~4.5 ± 2‰). CO2/3He ratios vary over 5 orders of magnitude from ~3 x 10^9 (MORB-like) to higher values (up to ~3 x 10^13) normally associated with crustal lithologies. Taken together, the He-CO2 data can be explained by 2-component mixing of a deep-seated mantle source with crustal component(s). There are no observed latitudinal isotopic trends in He-CO2. However, the two localities with MORB-like 3He/4He ratios ~6 to 7 RA, δ13C ~ -4 to -5 ‰ and CO2/3He ~ 4 x10^9 are both cold temperature (~ 15°C) CO2 gas vents. The MORB-like characteristics of these cold vents are comparable to MORB-like values observed at Oldoinyo Lengai in northern Tanzania [4], suggesting that both Rungwe region and Oldoinyo Lengai may derive their volatile compositions from a homogeneous (MORB-like) mantle source common to the entire segment of the southern EAR. [1] Furman (2007) Journal of African Earth Sciences 48, 147-160. [2] Ebinger et al. (1989) Journal of Geophysical Research 94, 15,785-15,803. [3] Pik et al. (2006) Chemical Geology 226, 100-114. [4] Fisher et al. (2009) Nature 459, 77-80.

  16. Production of sulfur gases and carbon dioxide by synthetic weathering of crushed drill cores from the Santa Cruz porphyry copper deposit near Casa Grande, Pinal County, Arizona

    USGS Publications Warehouse

    Hinkle, M.E.; Ryder, J.L.; Sutley, S.J.; Botinelly, T.

    1990-01-01

    Samples of ground drill cores from the southern part of the Santa Cruz porphyry copper deposit, Casa Grande, Arizona, were oxidized in simulated weathering experiments. The samples were also separated into various mineral fractions and analyzed for contents of metals and sulfide minerals. The principal sulfide mineral present was pyrite. Gases produced in the weathering experiments were measured by gas chromatography. Carbon dioxide, oxygen, carbonyl sulfide, sulfur dioxide and carbon disulfide were found in the gases; no hydrogen sulfide, organic sulfides, or mercaptans were detected. Oxygen concentration was very important for production of the volatiles measured; in general, oxygen concentration was more important to gas production than were metallic element content, sulfide mineral content, or mineral fraction (oxide or sulfide) of the sample. The various volatile species also appeared to be interactive; some of the volatiles measured may have been formed through gas reactions. ?? 1990.

  17. 40 CFR 60.33b - Emission guidelines for municipal waste combustor metals, acid gases, organics, and nitrogen oxides.

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ... discharged to the atmosphere from a designated facility is 27 milligrams per dry standard cubic meter... contained in the gases discharged to the atmosphere from a designated facility is 25 milligrams per dry... the gases discharged to the atmosphere from a designated facility is 10 percent (6-minute average)....

  18. 40 CFR 60.52b - Standards for municipal waste combustor metals, acid gases, organics, and nitrogen oxides.

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ... facility shall cause to be discharged into the atmosphere from that affected facility any gases that... operator of an affected facility shall cause to be discharged into the atmosphere from that affected... atmosphere from that affected facility any gases that contain cadmium in excess of the limits specified...

  19. 40 CFR 60.52b - Standards for municipal waste combustor metals, acid gases, organics, and nitrogen oxides.

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ... facility shall cause to be discharged into the atmosphere from that affected facility any gases that... operator of an affected facility shall cause to be discharged into the atmosphere from that affected... atmosphere from that affected facility any gases that contain cadmium in excess of the limits specified...

  20. Synthesis and Characterization of Poly(glyceric Acid Carbonate): A Degradable Analogue of Poly(acrylic Acid).

    PubMed

    Zhang, Heng; Lin, Xinrong; Chin, Stacy; Grinstaff, Mark W

    2015-10-01

    The synthesis and characterization of a degradable version of poly(acrylic acid), poly(glyceric acid carbonate), are reported. Specifically, atactic and isotactic poly(benzyl glycidate carbonate)s are obtained via the ring-opening copolymerization of rac-/(R)-benzyl glycidate with CO2 using a bifunctional rac-/(S,S)-cobalt salen catalyst in high carbonate linkage selectivity (>99%) and polymer/cyclic carbonate selectivity (∼90%). Atactic poly(benzyl glycidate carbonate) is an amorphous material with a T(g) (glass transition temperature) of 44 °C, while its isotactic counterpart synthesized from enantiopure epoxide and catalyst is semicrystalline with a T(m) (melting temperature) = 87 °C. Hydrogenolysis of the resultant polymers affords the poly(glyceric acid carbonate). Poly(glyceric acid carbonate) exhibits an improved cell cytotoxicity profile compared to poly(acrylic acid). Poly(glyceric acid carbonate)s also degrade remarkably fast (t(1/2) ≈ 2 weeks) compared to poly(acrylic acid). Cross-linked hydrogels prepared from poly(glyceric acid carbonate) and poly(ethylene glycol) diaziridine show significant degradation in pH 8.4 aqueous buffer solution compared to similarly prepared hydrogels from poly(acrylic acid) and poly(ethylene glycol) diaziridine. PMID:26378624

  1. CARBON CONTRIBUTION AND CHARACTERISTICS OF HUMIC ACID, FULVIC ACID, PARTICULATE ORGANIC MATTER AND GLOMALIN IN DIVERSE ECOSYSTEMS

    Technology Transfer Automated Retrieval System (TEKTRAN)

    Global climate change and soil carbon sequestration issues are entering the forefront of public policy, and emphasis is growing for research on carbon sinks and long-term terrestrial carbon stabilization. Humic acid (HA), fulvic acid (FA), humin and particulate organic matter (POM) have traditionall...

  2. NOBLE GASES

    EPA Science Inventory

    The Noble Gases symposium, on which this report is based, provided comprehensive coverage of the noble gases. The coverage included, but was not limited to, the properties, biokinetics, bioeffects, production and release to the environment, detection techniques, standards, and ap...

  3. Direct synthesis of formic acid from carbon dioxide by hydrogenation in acidic media.

    PubMed

    Moret, Séverine; Dyson, Paul J; Laurenczy, Gábor

    2014-01-01

    The chemical transformation of carbon dioxide into useful products becomes increasingly important as CO2 levels in the atmosphere continue to rise as a consequence of human activities. In this article we describe the direct hydrogenation of CO2 into formic acid using a homogeneous ruthenium catalyst, in aqueous solution and in dimethyl sulphoxide (DMSO), without any additives. In water, at 40 °C, 0.2 M formic acid can be obtained under 200 bar, however, in DMSO the same catalyst affords 1.9 M formic acid. In both solvents the catalysts can be reused multiple times without a decrease in activity. Worldwide demand for formic acid continues to grow, especially in the context of a renewable energy hydrogen carrier, and its production from CO2 without base, via the direct catalytic carbon dioxide hydrogenation, is considerably more sustainable than the existing routes. PMID:24886955

  4. Direct synthesis of formic acid from carbon dioxide by hydrogenation in acidic media

    PubMed Central

    Moret, Séverine; Dyson, Paul J.; Laurenczy, Gábor

    2014-01-01

    The chemical transformation of carbon dioxide into useful products becomes increasingly important as CO2 levels in the atmosphere continue to rise as a consequence of human activities. In this article we describe the direct hydrogenation of CO2 into formic acid using a homogeneous ruthenium catalyst, in aqueous solution and in dimethyl sulphoxide (DMSO), without any additives. In water, at 40 °C, 0.2 M formic acid can be obtained under 200 bar, however, in DMSO the same catalyst affords 1.9 M formic acid. In both solvents the catalysts can be reused multiple times without a decrease in activity. Worldwide demand for formic acid continues to grow, especially in the context of a renewable energy hydrogen carrier, and its production from CO2 without base, via the direct catalytic carbon dioxide hydrogenation, is considerably more sustainable than the existing routes. PMID:24886955

  5. Sulfur recovery from low hydrogen sulfide gases

    SciTech Connect

    Chute, A.E.

    1982-10-01

    Describes processes for recovering sulfur from acid gases containing less hydrogen sulfide than can be processed satisfactorily in a typical Claus sulfur recovery unit (as shown in diagram). One feature of the Recycle Selectox process is that the circulating gas acts like a flywheel to maintain steady operating conditions, even when the acid gas feed fluctuates. When the acid gas concentration falls below that which can be handled in a Claus or Selectox plant, direct conversion in a Stretford of similar process such as Unisulf is indicated. When the acid gases are weak in hydrogen sulfide, there are several considerations in conditioning the feed gas. Most of the hydrocarbons entering a Clause plant are oxidized to water and oxides of carbon. The weaker the acid gas feed, the greater is the advantage in using the Recycle Selectox process. Below 30%, the sulfur-burning Claus process can be applied. At 30% and lower, or even at higher concentrations, the Recycle Selectox or Selectox process offers a simpler yet effective means of converting and recovering sulfur. Concludes that simple modifications to the Claus process are adequate to convert hydrogen sulfide to elemental sulfur from reasonably prepared acid gases (CO/sub 2/ + H/sub 2/S) having hydrogen sulfide concentrations as low as 30%.

  6. Fixed bed adsorption of acid dyes onto activated carbon.

    PubMed

    Walker, G M; Weatherley, L R

    1998-01-01

    The context of the study here is the adsorption of acid dyes from wastewater arising from a nylon carpet printing plant which currently receives no treatment. Since nylon is a particularly difficult fibre to dye, acid dyes are required for successful coloration. However, their presence, in high concentrations, in aqueous effluent arising from the plant can create major problems with respect to disposal. A treatment method based on adsorption onto granular activated carbon (GAC F400) in a fixed column configuration is described and breakthrough data of the dyes determined. The breakthrough data were correlated using a model based on liquid and pore diffusion with a good fit of experimental results obtained. Trends in the effective diffusivity used in the model correlated with other authors. A slight decrease in effective diffusivity was found with decrease in particle size and was attributed to interactions between the relatively large molecular sized dye and the microspore structure found in granular activated carbon. PMID:15093338

  7. Karstification without carbonic acid: bedrock dissolution by gypsum- driven dedolomitization

    USGS Publications Warehouse

    Bischoff, J.L.; Julia, R.; Shanks, Wayne C.; Rosenbauer, R.J.

    1994-01-01

    The primary karst-forming process at Lake Banyoles is dedolomitization of basement rocks driven by gypsum dissolution. Karstification takes place along the subsurface contact between the gypsiferous Beuda Formation and the dolomitic Perafita Formation. This process is here recognized for the first time to cause karstification on a large scale; this is significant because it proceeds without the addition of soil-generated carbonic acid. -from Authors

  8. Carbon Isotope Ratios in Crassulacean Acid Metabolism Plants

    PubMed Central

    Szarek, Stan R.; Troughton, John H.

    1976-01-01

    A year round study of photosynthesis and carbon isotope fractionation was conducted with plants of Opuntia phaeacantha Engelm. and Yucca baccata Torr. occurring in natural stands at elevations of 525, 970, 1450 and 1900 m. Plant water potentials and the daytime pattern of 14CO2 photosynthesis were similar for all cacti along the elevational gradient, despite significant differences in temperature regime and soil water status. Carbon isotope ratios of total tissue and soluble extract fractions were relatively constant throughtout the entire year. Additionally, the ?13C values were similar in all plants of the same species along the elevational gradient, i.e. ?12.5 0.86 for O. phaeacantha and ?15.7 0.95 for Y. baccata. The results of this study indicate Crassulacean acid metabolism predominates as the major carbon pathway of these plants, which do not facultatively utilize the reductive pentose phosphate cycle of photosynthesis as the primary carboxylation reaction. PMID:16659680

  9. Adsorption of naphthenic acids on high surface area activated carbons.

    PubMed

    Iranmanesh, Sobhan; Harding, Thomas; Abedi, Jalal; Seyedeyn-Azad, Fakhry; Layzell, David B

    2014-01-01

    In oil sands mining extraction, water is an essential component; however, the processed water becomes contaminated through contact with the bitumen at high temperature, and a portion of it cannot be recycled and ends up in tailing ponds. The removal of naphthenic acids (NAs) from tailing pond water is crucial, as they are corrosive and toxic and provide a substrate for microbial activity that can give rise to methane, which is a potent greenhouse gas. In this study, the conversion of sawdust into an activated carbon (AC) that could be used to remove NAs from tailings water was studied. After producing biochar from sawdust by a slow-pyrolysis process, the biochar was physically activated using carbon dioxide (CO2) over a range of temperatures or prior to producing biochar, and the sawdust was chemically activated using phosphoric acid (H3PO4). The physically activated carbon had a lower surface area per gram than the chemically activated carbon. The physically produced ACs had a lower surface area per gram than chemically produced AC. In the adsorption tests with NAs, up to 35mg of NAs was removed from the water per gram of AC. The chemically treated ACs showed better uptake, which can be attributed to its higher surface area and increased mesopore size when compared with the physically treated AC. Both the chemically produced and physically produced AC provided better uptake than the commercially AC. PMID:24766592

  10. Biosynthesis of 2-hydroxyisobutyric acid (2-HIBA) from renewable carbon.

    PubMed

    Rohwerder, Thore; Müller, Roland H

    2010-01-01

    Nowadays a growing demand for green chemicals and cleantech solutions is motivating the industry to strive for biobased building blocks. We have identified the tertiary carbon atom-containing 2-hydroxyisobutyric acid (2-HIBA) as an interesting building block for polymer synthesis. Starting from this carboxylic acid, practically all compounds possessing the isobutane structure are accessible by simple chemical conversions, e. g. the commodity methacrylic acid as well as isobutylene glycol and oxide. During recent years, biotechnological routes to 2-HIBA acid have been proposed and significant progress in elucidating the underlying biochemistry has been made. Besides biohydrolysis and biooxidation, now a bioisomerization reaction can be employed, converting the common metabolite 3-hydroxybutyric acid to 2-HIBA by a novel cobalamin-dependent CoA-carbonyl mutase. The latter reaction has recently been discovered in the course of elucidating the degradation pathway of the groundwater pollutant methyl tert-butyl ether (MTBE) in the new bacterial species Aquincola tertiaricarbonis. This discovery opens the ground for developing a completely biotechnological process for producing 2-HIBA. The mutase enzyme has to be active in a suitable biological system producing 3-hydroxybutyryl-CoA, which is the precursor of the well-known bacterial bioplastic polyhydroxybutyrate (PHB). This connection to the PHB metabolism is a great advantage as its underlying biochemistry and physiology is well understood and can easily be adopted towards producing 2-HIBA. This review highlights the potential of these discoveries for a large-scale 2-HIBA biosynthesis from renewable carbon, replacing conventional chemistry as synthesis route and petrochemicals as carbon source. PMID:20184738

  11. Biosynthesis of 2-hydroxyisobutyric acid (2-HIBA) from renewable carbon

    PubMed Central

    2010-01-01

    Nowadays a growing demand for green chemicals and cleantech solutions is motivating the industry to strive for biobased building blocks. We have identified the tertiary carbon atom-containing 2-hydroxyisobutyric acid (2-HIBA) as an interesting building block for polymer synthesis. Starting from this carboxylic acid, practically all compounds possessing the isobutane structure are accessible by simple chemical conversions, e. g. the commodity methacrylic acid as well as isobutylene glycol and oxide. During recent years, biotechnological routes to 2-HIBA acid have been proposed and significant progress in elucidating the underlying biochemistry has been made. Besides biohydrolysis and biooxidation, now a bioisomerization reaction can be employed, converting the common metabolite 3-hydroxybutyric acid to 2-HIBA by a novel cobalamin-dependent CoA-carbonyl mutase. The latter reaction has recently been discovered in the course of elucidating the degradation pathway of the groundwater pollutant methyl tert-butyl ether (MTBE) in the new bacterial species Aquincola tertiaricarbonis. This discovery opens the ground for developing a completely biotechnological process for producing 2-HIBA. The mutase enzyme has to be active in a suitable biological system producing 3-hydroxybutyryl-CoA, which is the precursor of the well-known bacterial bioplastic polyhydroxybutyrate (PHB). This connection to the PHB metabolism is a great advantage as its underlying biochemistry and physiology is well understood and can easily be adopted towards producing 2-HIBA. This review highlights the potential of these discoveries for a large-scale 2-HIBA biosynthesis from renewable carbon, replacing conventional chemistry as synthesis route and petrochemicals as carbon source. PMID:20184738

  12. REACTIONS OF CHLORITE WITH ACTIVATED CARBON AND WITH VANILLIC ACID AND INDAN ADSORBED ON ACTIVATED CARBON

    EPA Science Inventory

    The reaction between chlorite (CO2(-1)) and vanillic acid, at pH 6.0 in the presence of granular activated carbon (GAC), yielded several reaction products identifiable by GC/MS; no products were found in the absence of GAC. Indan and ClO2 or ClO2(-1) reacted in aqueous solution a...

  13. Fullerenes: A New Carrier Phase for Noble Gases in Meteorites

    NASA Technical Reports Server (NTRS)

    Becker, Luann

    2004-01-01

    The major focus of our research effort has been to measure the noble gases encapsulated within fullerenes, a new carbon carrier phase and compare it to the myriad of components found in the bulk meteorite acid residues. We have concentrated on the carbonaceous chondrites (Allende, Murchison and Tagish Lake) since they have abundant noble gases, typically with a planetary signature that dominates the stepped-release of the meteorite bulk acid residue. They also contain an extractable fullerene component that can be isolated and purified from the same bulk material.

  14. Techniques for the analysis of gases sequentially released from lunar samples

    NASA Technical Reports Server (NTRS)

    Desmarais, D. J.; Hayes, J. M.; Meinschein, W. G.

    1973-01-01

    Description of two methods for the analysis of light gases that are sequentially evolved from 2 to 10 mg of lunar sample. A hydrofluoric acid hydrolysis of lunar material is achieved by repeated exposure of the sample to hydrogen fluoride. In the second technique, gases are evolved from lunar samples by the stepwise heating of these samples to 1400 C. The gases evolved by either hydrolysis or pyrolysis are analyzed in a gas chromatographic system using a helium ionization detector. The sensitivities of this detector for the gases, as analyzed, range from 20 picograms/sec for hydrogen to 0.2 picogram/sec for carbon dioxide.

  15. Amino acids of the Murchison meteorite. II - Five carbon acyclic primary beta-, gamma-, and delta-amino alkanoic acids

    NASA Technical Reports Server (NTRS)

    Cronin, J. R.; Pizzarello, S.; Yuen, G. U.

    1985-01-01

    The five-carbon acyclic primary beta, gamma, and delta amino alkanoic acids of the Murchison meteorite are studied using gas chromatography-mass spectrometry and ion exchange chromatography. The chromatograms reveal that alpha is the most abundant monoamino alkanoic acid followed by gamma and beta, and an exponential increase in the amount of amino acid is observed as the carbon number increases in the homologous series. The influence of frictional heating, spontaneous thermal decomposition, and radiation of the synthesis of amino acids is examined. The data obtained support an amino acid synthesis process involving random combination of single-carbon precursors.

  16. Remote Sensing Observations of Greenhouse Gases from space based and airborne platforms: from SCIAMACHY and MaMap to CarbonSat

    NASA Astrophysics Data System (ADS)

    Burrows, John P.; Schneising, Oliver; Buchwitz, Michael; Bovensmann, Heinrich; Heymann, Jens; Gerilowski, Konstantin; Krings, Thomas; Krautwurst, Sven; Dickerson, Russ

    2015-04-01

    Methane, CH4, e and carbon dioxide, CO2, play an important role in the earth carbon cycle. They are the two most important long lived greenhouse gases produced by anthropogenic fossil fuel combustion. In order to assess accurately the surface fluxes of CH4 or CO2. The Scanning Imaging Absorption Spectrometer for Atmospheric ChartographY, SCIAMACHY, was a national contribution to the ESA Envisat platform: the latter being launched on the 28th February 2002 and operating successfully until April 2012. The SCIAMACHY measurements of the up-welling radiation have been used to retrieve the dry mole fraction of XCH4 and XCO2, providing a unique 10 year record at the spatial resolution of 60 kmx30 km. This data has been used to observe the changing CH4 abundance in the atmosphere and identify anthropogenic such as Fracking and natural sources such as wetlands. The Methane and carbon dioxide Mapper, MaMap, was developed as an aircraft demonstration instrument for our CarbonSat and CarbonSat Constellation concepts. CarbonSat is in Phase A B1 studies as one of two candidate missions for ESA's Earth Explorer 8 Mission. Selected results from SCIAMACHY and Mamap will be presented with a focus on methane and the perspective for CarbonSat.

  17. A Bio-Inspired Two-Layer Sensing Structure of Polypeptide and Multiple-Walled Carbon Nanotube to Sense Small Molecular Gases

    PubMed Central

    Wang, Li-Chun; Su, Tseng-Hsiung; Ho, Cheng-Long; Yang, Shang-Ren; Chiu, Shih-Wen; Kuo, Han-Wen; Tang, Kea-Tiong

    2015-01-01

    In this paper, we propose a bio-inspired, two-layer, multiple-walled carbon nanotube (MWCNT)-polypeptide composite sensing device. The MWCNT serves as a responsive and conductive layer, and the nonselective polypeptide (40 mer) coating the top of the MWCNT acts as a filter into which small molecular gases pass. Instead of using selective peptides to sense specific odorants, we propose using nonselective, peptide-based sensors to monitor various types of volatile organic compounds. In this study, depending on gas interaction and molecular sizes, the randomly selected polypeptide enabled the recognition of certain polar volatile chemical vapors, such as amines, and the improved discernment of low-concentration gases. The results of our investigation demonstrated that the polypeptide-coated sensors can detect ammonia at a level of several hundred ppm and barely responded to triethylamine. PMID:25751078

  18. A bio-inspired two-layer sensing structure of polypeptide and multiple-walled carbon nanotube to sense small molecular gases.

    PubMed

    Wang, Li-Chun; Su, Tseng-Hsiung; Ho, Cheng-Long; Yang, Shang-Ren; Chiu, Shih-Wen; Kuo, Han-Wen; Tang, Kea-Tiong

    2015-01-01

    In this paper, we propose a bio-inspired, two-layer, multiple-walled carbon nanotube (MWCNT)-polypeptide composite sensing device. The MWCNT serves as a responsive and conductive layer, and the nonselective polypeptide (40 mer) coating the top of the MWCNT acts as a filter into which small molecular gases pass. Instead of using selective peptides to sense specific odorants, we propose using nonselective, peptide-based sensors to monitor various types of volatile organic compounds. In this study, depending on gas interaction and molecular sizes, the randomly selected polypeptide enabled the recognition of certain polar volatile chemical vapors, such as amines, and the improved discernment of low-concentration gases. The results of our investigation demonstrated that the polypeptide-coated sensors can detect ammonia at a level of several hundred ppm and barely responded to triethylamine. PMID:25751078

  19. Carbon dioxide generated from carbonates and acids for sampling blood-feeding arthropods.

    PubMed

    Burkett-Cadena, Nathan D; Blosser, Erik M; Young, Ryan M; To, Laurent D; Unnasch, Thomas R

    2015-09-01

    Carbon dioxide (CO2) is utilized to attract mosquitoes and other blood-feeding arthropods to traps around the world. Commercial forms of CO2 (e.g., dry ice and compressed gas) are often unavailable or extremely expensive in developing nations, where vector surveillance is essential to make life-saving decisions. We developed and tested inexpensive and reproducible methods of CO2 production from the combination of acids and carbonates, ranging from very basic (crushed seashells and vinegar) to relatively elaborate (a device that controls the timing of the acid-carbonate reaction and extends the reaction over several hours). When utilized with mosquito traps in Florida, USA and black fly traps in Region des Cascades, Burkina Faso, these carbonate-acid CO2 sources attracted significantly greater numbers of both vector groups, than did unbaited traps. CO2 was generated for more than four hours at levels sufficient to attract vectors over the entire period. The utility of this simple methodology in developing nations should be further evaluated. PMID:26103427

  20. Removal of Particles and Acid Gases (SO2 or HCl) with a Ceramic Filter by Addition of Dry Sorbents

    SciTech Connect

    Hemmer, G.; Kasper, G.; Wang, J.; Schaub, G.

    2002-09-20

    The present investigation intends to add to the fundamental process design know-how for dry flue gas cleaning, especially with respect to process flexibility, in cases where variations in the type of fuel and thus in concentration of contaminants in the flue gas require optimization of operating conditions. In particular, temperature effects of the physical and chemical processes occurring simultaneously in the gas-particle dispersion and in the filter cake/filter medium are investigated in order to improve the predictive capabilities for identifying optimum operating conditions. Sodium bicarbonate (NaHCO{sub 3}) and calcium hydroxide (Ca(OH){sub 2}) are known as efficient sorbents for neutralizing acid flue gas components such as HCl, HF, and SO{sub 2}. According to their physical properties (e.g. porosity, pore size) and chemical behavior (e.g. thermal decomposition, reactivity for gas-solid reactions), optimum conditions for their application vary widely. The results presented concentrate on the development of quantitative data for filtration stability and overall removal efficiency as affected by operating temperature. Experiments were performed in a small pilot unit with a ceramic filter disk of the type Dia-Schumalith 10-20 (Fig. 1, described in more detail in Hemmer 2002 and Hemmer et al. 1999), using model flue gases containing SO{sub 2} and HCl, flyash from wood bark combustion, and NaHCO{sub 3} as well as Ca(OH){sub 2} as sorbent material (particle size d{sub 50}/d{sub 84} : 35/192 {micro}m, and 3.5/16, respectively). The pilot unit consists of an entrained flow reactor (gas duct) representing the raw gas volume of a filter house and the filter disk with a filter cake, operating continuously, simulating filter cake build-up and cleaning of the filter medium by jet pulse. Temperatures varied from 200 to 600 C, sorbent stoichiometric ratios from zero to 2, inlet concentrations were on the order of 500 to 700 mg/m{sup 3}, water vapor contents ranged from zero to 20 vol%. The experimental program with NaHCO{sub 3} is listed in Table 1. In addition, model calculations were carried out based on own and published experimental results that estimate residence time and temperature effects on removal efficiencies.

  1. Maintenance Carbon Cycle in Crassulacean Acid Metabolism Plant Leaves 1

    PubMed Central

    Kenyon, William H.; Severson, Ray F.; Black, Clanton C.

    1985-01-01

    The reciprocal relationship between diurnal changes in organic acid and storage carbohydrate was examined in the leaves of three Crassulacean acid metabolism plants. It was found that depletion of leaf hexoses at night was sufficient to account quantitatively for increase in malate in Ananas comosus but not in Sedum telephium or Kalancho daigremontiana. Fructose and to a lesser extent glucose underwent the largest changes. Glucose levels in S. telephium leaves oscillated diurnally but were not reciprocally related to malate fluctuations. Analysis of isolated protoplasts and vacuoles from leaves of A. comosus and S. telephium revealed that vacuoles contain a large percentage (>50%) of the protoplast glucose, fructose and malate, citrate, isocitrate, ascorbate and succinate. Sucrose, a major constituent of intact leaves, was not detectable or was at extremely low levels in protoplasts and vacuoles from both plants. In isolated vacuoles from both A. comosus and S. telephium, hexose levels decreased at night at the same time malate increased. Only in A. comosus, however, could hexose metabolism account for a significant amount of the nocturnal increase in malate. We conclude that, in A. comosus, soluble sugars are part of the daily maintenance carbon cycle and that the vacuole plays a dynamic role in the diurnal carbon assimilation cycle of this Crassulacean acid metabolism plant. PMID:16664005

  2. Electrochemical Determination of Glycoalkaloids Using a Carbon Nanotubes-Phenylboronic Acid Modified Glassy Carbon Electrode

    PubMed Central

    Wang, Huiying; Liu, Mingyue; Hu, Xinxi; Li, Mei; Xiong, Xingyao

    2013-01-01

    A versatile strategy for electrochemical determination of glycoalkaloids (GAs) was developed by using a carbon nanotubes-phenylboronic acid (CNTs-PBA) modified glassy carbon electrode. PBA reacts with ?-solanine and ?-chaconine to form a cyclic ester, which could be utilized to detect GAs. This method allowed GA detection from 1 ?M to 28 ?M and the detection limit was 0.3 ?M. Affinity interaction of GAs and immobilized PBA caused an essential change of the peak current. The CNT-PBA modified electrodes were sensitive for detection of GAs, and the peak current values were in quite good agreement with those measured by the sensors. PMID:24287539

  3. Online measurements of ammonia, acidic trace gases and aerosol inorganic ionic species in the Amazon Basin under biomass burning and background conditions

    NASA Astrophysics Data System (ADS)

    Trebs, I.; Meixner, F. X.; Otjes, R. P.; Slanina, J. J.; Jongejan, P. A. C.; Moura, M. A. L.; da Silva, R. S., Jr.; Mayol-Bracero, O. L.; Artaxo, P.; Andreae, M. O.

    2003-04-01

    We have measured diurnal and seasonal variations in the mixing ratios of ammonia (NH_3), nitric acid (HNO_3), nitrous acid (HNO_2), hydrochloric acid (HCl) and water-soluble inorganic aerosol species as ammonium (NH4+), nitrate (NO3-), nitrite (NO2-), chloride (Cl_-) and sulfate (SO_42-) on a pasture site in the Amazon Basin (Rondnia, Brazil) from September to November 2002 (LBA-SMOCC). Sampling was performed using a wet-annular denuder in combination with a Steam-Jet Aerosol Collector (SJAC) followed by online analysis using a mobile ion chromatograph for anions and flow injection analysis for ammonium. Measurements were supported by monitoring of meteorological parameters (e.g., relative humidity, air temperature, wind speed). Results from the biomass burning season, transition period and wet season will be presented. Preliminary evaluations show that ammonia levels were found to be highest (median values of 2.0 ppb during the biomass burning season), whereas median values for acidic trace gases were found to be an order of magnitude lower (0.2 ppb for nitric acid and 0.14 ppb for hydrochloric acid under biomass burning conditions). Preliminary results of aerosol species show that the mixing ratios were highest during the burning season (median values for ammonium ? 1.0 ppb, for nitrate ? 0.3 ppb, for nitrite ? 0.05 ppb, for chloride ? 0.1 ppb and for sulfate ? 0.25 ppb). The calculated median mixing ratio levels decreased steadily from the biomass burning season through the transition period to the wet season, by approximately 75% for trace gases and by 50% and 75% for aerosol ammonium and other inorganic aerosol species respectively. We found a strong dependence of ammonia, nitric acid, and aerosol ammonium nitrate on meteorological parameters (especially air temperature and relative humidity) as well as on daily/ nocturnal boundary layer conditions during day and night time. The diurnal data sets suggest that evaporation of ammonia and nitric acid from the aerosol surface contributes effectively to increased mixing ratios in the turbulent boundary layer at day time. Additionally, we found that a sharp increase of relative humidity to nearly 100% and a decrease of temperature from day to night time promotes the formation of aerosol ammonium nitrate due to gas-aerosol interactions. Both the soluble inorganic ionic species and soluble gases, such as NH_3 and HNO_3, are expected to play a major role in the nucleation and growth of cloud droplets under clean and polluted conditions.

  4. 40 CFR 60.52b - Standards for municipal waste combustor metals, acid gases, organics, and nitrogen oxides.

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... discharged into the atmosphere from the affected facility any gases that contain mercury in excess of the... potential mercury emission concentration (85-percent reduction by weight), corrected to 7 percent oxygen... percent of the potential mercury emission concentration (85-percent reduction by weight), corrected to...

  5. 40 CFR 62.14103 - Emission limits for municipal waste combustor metals, acid gases, organics, and nitrogen oxides.

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ... operator of an affected facility must not cause to be discharged into the atmosphere from that affected... operator of an affected facility must not cause to be discharged into the atmosphere from that affected... discharged into the atmosphere from that affected facility any gases that contain mercury in excess of...

  6. 40 CFR 62.14103 - Emission limits for municipal waste combustor metals, acid gases, organics, and nitrogen oxides.

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ... operator of an affected facility must not cause to be discharged into the atmosphere from that affected... operator of an affected facility must not cause to be discharged into the atmosphere from that affected... discharged into the atmosphere from that affected facility any gases that contain mercury in excess of...

  7. Reductive dechlorination of carbon tetrachloride using buffered alkaline ascorbic acid.

    PubMed

    Lin, Ya-Ting; Liang, Chenju

    2015-10-01

    Alkaline ascorbic acid (AA) was recently discovered as a novel in-situ chemical reduction (ISCR) reagent for remediating chlorinated solvents in the subsurface. For this ISCR process, the maintenance of an alkaline pH is essential. This study investigated the possibility of the reduction of carbon tetrachloride (CT) using alkaline AA solution buffered by phosphate and by NaOH. The results indicated that CT was reduced by AA, and chloroform (CF) was a major byproduct at a phosphate buffered pH of 12. However, CT was completely reduced by AA in 2M NaOH without CF formation. In the presence of iron/soil minerals, iron could be reduced by AA and Fe(2+) tends to precipitate on the mineral surface to accelerate CT degradation. A simultaneous transfer of hydrogenolysis and dichloroelimination would occur under phosphate buffered pH 12. This implies that a high alkaline environment is a crucial factor for maintaining the dominant pathway of two electron transfer from dianionic AA to dehydroascorbic acid, and to undergo dichloroelimination of CT. Moreover, threonic acid and oxalic acid were identified to be the major AA decomposition products in alkaline solutions. PMID:25912910

  8. Interaction of solid organic acids with carbon nanotube field effect transistors

    NASA Astrophysics Data System (ADS)

    Klinke, Christian; Afzali, Ali; Avouris, Phaedon

    2006-10-01

    A series of solid organic acids were used to p-dope carbon nanotubes. The extent of doping is shown to be dependent on the pKa value of the acids. Highly fluorinated carboxylic acids and sulfonic acids are very effective in shifting the threshold voltage and making carbon nanotube field effect transistors to be more p-type devices. Weaker acids like phosphonic or hydroxamic acids had less effect. The doping of the devices was accompanied by a reduction of the hysteresis in the transfer characteristics. In-solution doping survives standard fabrication processes and renders p-doped carbon nanotube field effect transistors with good transport characteristics.

  9. l-Lactic acid production from glycerol coupled with acetic acid metabolism by Enterococcus faecalis without carbon loss.

    PubMed

    Murakami, Nao; Oba, Mana; Iwamoto, Mariko; Tashiro, Yukihiro; Noguchi, Takuya; Bonkohara, Kaori; Abdel-Rahman, Mohamed Ali; Zendo, Takeshi; Shimoda, Mitsuya; Sakai, Kenji; Sonomoto, Kenji

    2016-01-01

    Glycerol is a by-product in the biodiesel production process and considered as one of the prospective carbon sources for microbial fermentation including lactic acid fermentation, which has received considerable interest due to its potential application. Enterococcus faecalis isolated in our laboratory produced optically pure l-lactic acid from glycerol in the presence of acetic acid. Gas chromatography-mass spectrometry analysis using [1, 2-(13)C2] acetic acid proved that the E. faecalis strain QU 11 was capable of converting acetic acid to ethanol during lactic acid fermentation of glycerol. This indicated that strain QU 11 restored the redox balance by oxidizing excess NADH though acetic acid metabolism, during ethanol production, which resulted in lactic acid production from glycerol. The effects of pH control and substrate concentration on lactic acid fermentation were also investigated. Glycerol and acetic acid concentrations of 30 g/L and 10 g/L, respectively, were expected to be appropriate for lactic acid fermentation of glycerol by strain QU 11 at a pH of 6.5. Furthermore, fed-batch fermentation with 30 g/L glycerol and 10 g/L acetic acid wholly exhibited the best performance including lactic acid production (55.3 g/L), lactic acid yield (0.991 mol-lactic acid/mol-glycerol), total yield [1.08 mol-(lactic acid and ethanol)]/mol-(glycerol and acetic acid)], and total carbon yield [1.06 C-mol-(lactic acid and ethanol)/C-mol-(glycerol and acetic acid)] of lactic acid and ethanol. In summary, the strain QU 11 successfully produced lactic acid from glycerol with acetic acid metabolism, and an efficient fermentation system was established without carbon loss. PMID:26168904

  10. Activated carbon passes tests for acid-gas cleanup

    SciTech Connect

    Harruff, L.G.; Bushkuhl, S.J.

    1996-06-24

    Use of activated carbon to remove hydrocarbon contaminants from the acid-gas feed to Claus sulfur-recovery units has been successfully pilot tested in Saudi Arabia. Pilot plant results are discussed here along with issues involved in scale-up to commercial size. Heavy hydrocarbons, particularly benzene, toluene, and xylene (BTX) have been linked to coke formation and catalyst deactivation in Claus converters. This deactivation results in reduced sulfur recovery and increased sulfur emissions from these plants. This clean-up process was proven to be capable of removing 95% of the BTX and other C{sub 6}+s from acid gas over a wide range of actual plant conditions. Following the adsorption step, the activated carbon was easily regenerated by use of low-pressure steam. A post-regeneration drying step using plant fuel gas also proved beneficial. The paper discusses feed contaminants, vapor-phase cleanup, testing design, test parameters and results, bed drying after regeneration, regeneration conditions, basic flow, system control, and full-scale installation.

  11. Hydrogen storage and delivery: the carbon dioxide - formic acid couple.

    PubMed

    Laurenczy, Gábor

    2011-01-01

    Carbon dioxide and the carbonates, the available natural C1 sources, can be easily hydrogenated into formic acid and formates in water; the rate of this reduction strongly depends on the pH of the solution. This reaction is catalysed by ruthenium(II) pre-catalyst complexes with a large variety of water-soluble phosphine ligands; high conversions and turnover numbers have been realised. Although ruthenium(II) is predominant in these reactions, the iron(II) - tris[(2-diphenylphosphino)-ethyl]phosphine (PP3) complex is also active, showing a new perspective to use abundant and inexpensive iron-based compounds in the CO2 reduction. In the catalytic hydrogenation cycles the in situ formed metal hydride complexes play a key role, their structures with several other intermediates have been proven by multinuclear NMR spectroscopy. In the other hand safe and convenient hydrogen storage and supply is the fundamental question for the further development of the hydrogen economy; and carbon dioxide has been recognised to be a viable H2 vector. Formic acid--containing 4.4 weight % of H2, that is 53 g hydrogen per litre--is suitable for H2 storage; we have shown that in aqueous solutions it can be selectively decomposed into CO-free (CO < 10 ppm) CO2 and H2. The reaction takes place under mild experimental conditions and it is able to generate high pressure H2 (up to 600 bar). The cleavage of HCOOH is catalysed by several hydrophilic Ru(II) phosphine complexes (meta-trisulfonated triphenylphosphine, mTPPTS, being the most efficient one), either in homogeneous systems or as immobilised catalysts. We have also shown that the iron(II)--hydrido tris[(2-diphenylphosphino)ethyl]phosphine complex catalyses with an exceptionally high rate and efficiency (turnover frequency, TOF = 9425 h(-1)mol(-1); turnover number, TON = 92400) the formic acid cleavage, in environmentally friendly propylene carbonate solution, opening the way to use cheap, non-noble metal based catalysts for this reaction, too. PMID:22026175

  12. Amino acids of the Murchison meteorite. I - Six carbon acyclic primary alpha-amino alkanoic acids

    NASA Technical Reports Server (NTRS)

    Cronin, J. R.; Gandy, W. E.; Pizzarello, S.

    1981-01-01

    Six of the seven chain isomers of six-carbon acyclic primary alpha-amino alkanoic acids (leucine isomers) have been either identified or confirmed in hot-water extracts of the Murchison meteorite using combined gas chromatography-mass spectrometry (GC-MS) and ion exchange chromatography. 2-Amino-2-ethylbutyric acid, 2-amino-2,3-dimethylbutyric acid, pseudoleucine, and 2-methylnorvaline were positively identified by GC-MS. These amino acids have not been previously reported to occur in natural materials and may be uniquely meteoritic in origin. The presence of leucine and isoleucine (including the diastereoisomer, alloisoleucine) was confirmed. Peaks corresponding to norleucine were seen by ion-exchange and gas chromatography but characteristic mass spectra were not obtained. The alpha-branched chain isomers in this series are quantitatively the most significant. These results are compared with literature data on amino acid synthesis by electrical discharge and Fischer-Tropsch-type catalysis. Neither model system produces an amino acid suite that is completely comparable to that found in the Murchison meteorite.

  13. Measurements of Acidic Gases and Aerosol Species Aboard the NASA DC-8 Aircraft During the Pacific Exploratory Mission in the Tropics (PEM-Tropics A)

    NASA Technical Reports Server (NTRS)

    Talbot, Robert W.; Dibb, Jack E.

    1999-01-01

    We received funding to provide measurements of nitric acid (HNO3), formic acid (HCOOH), acetic acid (CH3COOH), and the chemical composition of aerosols aboard the NASA Ames DC-8 research aircraft during the PEM-Tropics A mission. These measurements were successfully completed and the final data resides in the electronic archive (ftp-gte.larc.nasa.gov) at NASA Langley Research Center. For the PEM-Tropics A mission the University of New Hampshire group was first author of four different manuscripts. Three of these have now appeared in the Journal of Geophysical Research-Atmospheres, included in the two section sections on PEM-Tropics A. The fourth manuscript has just recently been submitted to this same journal as a stand alone paper. All four of these papers are included in this report. The first paper (Influence of biomass combustion emissions on the distribution of acidic trace gases over the Southern Pacific basin during austral springtime) describes the large-scale distributions of HNO3, HCOOH, and CH3COOH. Arguments were presented to show, particularly in the middle tropospheric region, that biomass burning emissions from South America and Africa were a major source of acidic gases over the South Pacific basin. The second paper (Aerosol chemical composition and distribution during the Pacific Exploratory Mission (PEM) Tropics) covers the aerosol aspects of our measurement package. Compared to acidic gases, O3, and selected hydrocarbons, the aerosol chemistry showed little influence from biomass burning emissions. The data collected in the marine boundary layer showed a possible marine source of NH3 to the troposphere in equatorial areas. This source had been speculated on previously, but our data was the first collected from an airborne platform to show its large-scale features. The third paper (Constraints on the age and dilution of Pacific Exploratory Mission-Tropics biomass burning plumes from the natural radionuclide tracer Pb-210) utilized the unexpectedly high concentrations of Pb-210 in the combustion plumes to estimate their ages and mixing along the transport route to the South Pacific basin. The final paper in the group (Tropospheric reactive-odd nitrogen over the South Pacific in austral springtime). This paper provides a summary of reactive nitrogen during PEM-Tropics A, with HNO3 and PAM showing the most impact from combustion emission.

  14. Hydropyrolysis as a preparative method for the compound-specific carbon isotope analysis of fatty acids.

    PubMed

    Sephton, Mark A; Meredith, Will; Sun, Cheng-Gong; Snape, Colin E

    2005-01-01

    Compound-specific stable carbon isotope analysis by gas chromatography/combustion/isotope ratio mass spectrometry is an effective and risk-free means of investigating fatty acid metabolism. Straightforward analysis, however, leads to poor chromatographic resolution, while derivatization adds carbon thereby corrupting the starting stable isotopic composition. Hydropyrolysis is a new approach which defunctionalizes fatty acids to yield the corresponding n-alkanes thus retaining the carbon skeleton intact and improving chromatography, allowing the faithful measurement of carbon isotope ratios. PMID:15645412

  15. Carbon composite micro- and nano-tubes-based electrodes for detection of nucleic acids

    NASA Astrophysics Data System (ADS)

    Prasek, Jan; Huska, Dalibor; Jasek, Ondrej; Zajickova, Lenka; Trnkova, Libuse; Adam, Vojtech; Kizek, Rene; Hubalek, Jaromir

    2011-05-01

    The first aim of this study was to fabricate vertically aligned multiwalled carbon nanotubes (MWCNTs). MWCNTs were successfully prepared by using plasma enhanced chemical vapour deposition. Further, three carbon composite electrodes with different content of carbon particles with various shapes and sizes were prepared and tested on measuring of nucleic acids. The dependences of adenine peak height on the concentration of nucleic acid sample were measured. Carbon composite electrode prepared from a mixture of glassy and spherical carbon powder and MWCNTs had the highest sensitivity to nucleic acids. Other interesting result is the fact that we were able to distinguish signals for all bases using this electrode.

  16. Carbon composite micro- and nano-tubes-based electrodes for detection of nucleic acids.

    PubMed

    Prasek, Jan; Huska, Dalibor; Jasek, Ondrej; Zajickova, Lenka; Trnkova, Libuse; Adam, Vojtech; Kizek, Rene; Hubalek, Jaromir

    2011-01-01

    The first aim of this study was to fabricate vertically aligned multiwalled carbon nanotubes (MWCNTs). MWCNTs were successfully prepared by using plasma enhanced chemical vapour deposition. Further, three carbon composite electrodes with different content of carbon particles with various shapes and sizes were prepared and tested on measuring of nucleic acids. The dependences of adenine peak height on the concentration of nucleic acid sample were measured. Carbon composite electrode prepared from a mixture of glassy and spherical carbon powder and MWCNTs had the highest sensitivity to nucleic acids. Other interesting result is the fact that we were able to distinguish signals for all bases using this electrode. PMID:21711910

  17. Carbon composite micro- and nano-tubes-based electrodes for detection of nucleic acids

    PubMed Central

    2011-01-01

    The first aim of this study was to fabricate vertically aligned multiwalled carbon nanotubes (MWCNTs). MWCNTs were successfully prepared by using plasma enhanced chemical vapour deposition. Further, three carbon composite electrodes with different content of carbon particles with various shapes and sizes were prepared and tested on measuring of nucleic acids. The dependences of adenine peak height on the concentration of nucleic acid sample were measured. Carbon composite electrode prepared from a mixture of glassy and spherical carbon powder and MWCNTs had the highest sensitivity to nucleic acids. Other interesting result is the fact that we were able to distinguish signals for all bases using this electrode. PMID:21711910

  18. Oxidant gases

    SciTech Connect

    Evans, M.J.

    1984-01-01

    The acute and chronic action of the oxidant gases ozone, nitrogen dioxide and oxygen on the morphological appearance of cells of the alveolar and bronchiolar epithelium is reviewed. Type I cells of the alveolar and ciliated cells of the bronchiolar epithelium appear to be sensitive targets for the oxidant gases. The degree of damage is influenced by age, nutritional status and the development of tolerance.

  19. A Simple Demonstration of Carbon Dioxide Fixation and Acid Production in CAM Plants

    ERIC Educational Resources Information Center

    Walker, John R. L.; McWha, James A.

    1976-01-01

    Described is an experiment investigating carbon dioxide fixation in the dark and the diurnal rhythm of acid production in plants exhibiting Crassulacean Acid Metabolism. Included are suggestions for four further investigations. (SL)

  20. Thermal device and method for production of carbon monoxide and hydrogen by thermal dissociation of hydrocarbon gases

    DOEpatents

    Detering, Brent A. (Idaho Falls, ID); Kong, Peter C. (Idaho Falls, ID)

    2001-01-01

    Carbon monoxide is produced in a fast quench reactor. The production of carbon monoxide includes injecting carbon dioxide and some air into a reactor chamber having a high temperature at its inlet and a rapidly expanding a reactant stream, such as a restrictive convergent-divergent nozzle at its outlet end. Carbon dioxide and other reactants such as methane and other low molecular weight hydrocarbons are injected into the reactor chamber. Other gas may be added at different stages in the process to form a desired end product and prevent back reactions. The resulting heated gaseous stream is then rapidly cooled by expansion of the gaseous stream.

  1. Dynamics of submarine groundwater discharge and associated fluxes of dissolved nutrients, carbon, and trace gases to the coastal zone (Okatee River estuary, South Carolina)

    USGS Publications Warehouse

    Porubsky, W.P.; Weston, N.B.; Moore, W.S.; Ruppel, C.; Joye, S.B.

    2014-01-01

    Multiple techniques, including thermal infrared aerial remote sensing, geophysical and geological data, geochemical characterization and radium isotopes, were used to evaluate the role of groundwater as a source of dissolved nutrients, carbon, and trace gases to the Okatee River estuary, South Carolina. Thermal infrared aerial remote sensing surveys illustrated the presence of multiple submarine groundwater discharge sites in Okatee headwaters. Significant relationships were observed between groundwater geochemical constituents and 226Ra activity in groundwater with higher 226Ra activity correlated to higher concentrations of organics, dissolved inorganic carbon, nutrients, and trace gases to the Okatee system. A system-level radium mass balance confirmed a substantial submarine groundwater discharge contribution of these constituents to the Okatee River. Diffusive benthic flux measurements and potential denitrification rate assays tracked the fate of constituents in creek bank sediments. Diffusive benthic fluxes were substantially lower than calculated radium-based submarine groundwater discharge inputs, showing that advection of groundwater-derived nutrients dominated fluxes in the system. While a considerable potential for denitrification in tidal creek bank sediments was noted, in situ denitrification rates were nitrate-limited, making intertidal sediments an inefficient nitrogen sink in this system. Groundwater geochemical data indicated significant differences in groundwater chemical composition and radium activity ratios between the eastern and western sides of the river; these likely arose from the distinct hydrological regimes observed in each area. Groundwater from the western side of the Okatee headwaters was characterized by higher concentrations of dissolved organic and inorganic carbon, dissolved organic nitrogen, inorganic nutrients and reduced metabolites and trace gases, i.e. methane and nitrous oxide, than groundwater from the eastern side. Differences in microbial sulfate reduction, organic matter supply, and/or groundwater residence time likely contributed to this pattern. The contrasting features of the east and west sub-marsh zones highlight the need for multiple techniques for characterization of submarine groundwater discharge sources and the impact of biogeochemical processes on the delivery of nutrients and carbon to coastal areas via submarine groundwater discharge.

  2. Dynamics of submarine groundwater discharge and associated fluxes of dissolved nutrients, carbon, and trace gases to the coastal zone (Okatee River estuary, South Carolina)

    NASA Astrophysics Data System (ADS)

    Porubsky, W. P.; Weston, N. B.; Moore, W. S.; Ruppel, C.; Joye, S. B.

    2014-04-01

    Multiple techniques, including thermal infrared aerial remote sensing, geophysical and geological data, geochemical characterization and radium isotopes, were used to evaluate the role of groundwater as a source of dissolved nutrients, carbon, and trace gases to the Okatee River estuary, South Carolina. Thermal infrared aerial remote sensing surveys illustrated the presence of multiple submarine groundwater discharge sites in Okatee headwaters. Significant relationships were observed between groundwater geochemical constituents and 226Ra activity in groundwater with higher 226Ra activity correlated to higher concentrations of organics, dissolved inorganic carbon, nutrients, and trace gases to the Okatee system. A system-level radium mass balance confirmed a substantial submarine groundwater discharge contribution of these constituents to the Okatee River. Diffusive benthic flux measurements and potential denitrification rate assays tracked the fate of constituents in creek bank sediments. Diffusive benthic fluxes were substantially lower than calculated radium-based submarine groundwater discharge inputs, showing that advection of groundwater-derived nutrients dominated fluxes in the system. While a considerable potential for denitrification in tidal creek bank sediments was noted, in situ denitrification rates were nitrate-limited, making intertidal sediments an inefficient nitrogen sink in this system. Groundwater geochemical data indicated significant differences in groundwater chemical composition and radium activity ratios between the eastern and western sides of the river; these likely arose from the distinct hydrological regimes observed in each area. Groundwater from the western side of the Okatee headwaters was characterized by higher concentrations of dissolved organic and inorganic carbon, dissolved organic nitrogen, inorganic nutrients and reduced metabolites and trace gases, i.e. methane and nitrous oxide, than groundwater from the eastern side. Differences in microbial sulfate reduction, organic matter supply, and/or groundwater residence time likely contributed to this pattern. The contrasting features of the east and west sub-marsh zones highlight the need for multiple techniques for characterization of submarine groundwater discharge sources and the impact of biogeochemical processes on the delivery of nutrients and carbon to coastal areas via submarine groundwater discharge.

  3. The natural flux of greenhouse gases in the case of monitoring the flux of juvenile carbon dioxide in the Hranice Karst

    NASA Astrophysics Data System (ADS)

    Geršl, Milan; Stepišnik, Uroš; Mareček, Jan; Geršlová, Eva; Hammerschmiedt, Michal

    2015-04-01

    Located in the Teplice nad Bečvou district 40 km SE of Olomouc (Czech Republic), the hydrothermal Hranice Karst with the Zbrašov Aragonite Caves has been developed in the sequence of Palaeozoic limestones as a result of deep influx of thermal water charged with subcrustal carbon dioxide (CO2). This area of discharge of juvenile carbon dioxide is a unique place where one can study the long-term natural production of a greenhouse gas and confront it with the anthropogenic production. As a result, the continuous measurements of the properties of the cave microclimate with additional seasonal measurements of flux of carbon dioxide give rise to a rare pool of data that cover natural routes of greenhouse gases. Repeated seasonal analysis of the ratio of stable carbon isotopes in carbon dioxide (d13C around -5 ) (Meyberg - Rinne, 1995)has suggested the juvenile (mantle) origin of this gas. Isotopic analyses in the mineral water of dissolved gases (He) show that some part of these gases come from the upper mantle of the Earth. The lower floors of the caves are filled with carbon dioxide producing so-called gas lakes in the area. Concentrations of the gas commonly reach 40 % by volume. In 1999, for example, the average concentration in the Gallas dome was 84.9 % by volume. Flux of CO2 (g.m-2.d-1) was measured on the surface and in the cave. The homogenisation chamber and the pumping test were applied to evaluate the CO2 flux. The average CO2 flux in the soil ranged from 74 to 125 g.m-2.d-1, reflecting the venting of subcrustal CO2 in the Hranice area (Geršl et al., 2012). In the Zbrašov Aragonite Caves the CO2 concentration in the atmosphere fluctuates from 0,X to 85 % with the measured constant flux being 32 894 g.m-2.d-1. Since 2005, the CO2 concentrations in the cave area have been reported by an automatic monitoring system at 10 cave sites. CO2 concentrations are recorded in 5-min intervals. Interpretation can be put into the context of measuring concentrations of Rn, groundwater levels, and influence of the ambient conditions on the cave system and the operation of the visitor trail. The data obtained are an exceptional source of information about the behaviour of natural emissions of a greenhouse gas in the form of juvenile carbon dioxide. The hydrothermal speleothems carry unique information about production of carbon dioxide in the studied area. Based on their dating using the 230Th/234U method it can be deduced indirectly that the carbon dioxide emissions occurred as early as 84-127 thousand years ago in the area. The research was conducted with the support of the project entitled "Postdoc contracts at MENDELU technical and ekonomical research' (CZ.1.07/2.3.00/30.0031). Geršl, M. - Geršlová, E. - Šimečková, B. (2012): Subcrustal CO2 flux measurement in the Hranice hydrothermal Karst, methodology and first results. - Geoscience research reports for 2011, 45, D, 162-166. Praha. Meyberg, M. - Rinne, B. (1995): Messung des 3He/4He-Isotopenverhältnisses im Hranicka Propast (Tschechische Republik). - Die Höhle. Zeitschrift für Karst- und Höhlenkunde, 46, 1, 5-8. Wien.

  4. [The subacute toxicity of glucosylthiazolidine-4-carbonic acid in rats].

    PubMed

    Lewerenz, H J; Plass, R; Bleyl, D W; Macholz, R; Zeise, S; Kroh, L

    1990-01-01

    Glucosylthiazolidine-4-carbonic acid, an intermediate of the Maillard reaction between D-glucose and L-cysteine, was given in doses of 0, 25, 50 or 100 mg/kg b.w. by oral intubation to male and female rats for 21 days. General appearance, growth, food consumption, haematology, urine analysis and serum chemistry including determinations of enzyme activities, organ weights and macroscopic and microscopic pathology were used as criteria for adverse effects. Effects on the kidneys were indicated by oliguria and decreased specific gravity of the urine in males and histopathological changes of the proximal tubules in females. The no-effect dose established from this study is 25 mg/kg b.w. PMID:2089262

  5. In situ synthesis carbonated hydroxyapatite layers on enamel slices with acidic amino acids by a novel two-step method.

    PubMed

    Wu, Xiaoguang; Zhao, Xu; Li, Yi; Yang, Tao; Yan, Xiujuan; Wang, Ke

    2015-09-01

    In situ fabrication of carbonated hydroxyapatite (CHA) remineralization layer on an enamel slice was completed in a novel, biomimetic two-step method. First, a CaCO3 layer was synthesized on the surface of demineralized enamel using an acidic amino acid (aspartic acid or glutamate acid) as a soft template. Second, at the same concentration of the acidic amino acid, rod-like carbonated hydroxyapatite was produced with the CaCO3 layer as a sacrificial template and a reactant. The morphology, crystallinity and other physicochemical properties of the crystals were characterized using field emission scanning electron microscopy (FESEM), Fourier transform infrared spectrometry (FTIR), X-ray diffraction (XRD) and energy-dispersive X-ray analysis (EDAX), respectively. Acidic amino acid could promote the uniform deposition of hydroxyapatite with rod-like crystals via absorption of phosphate and carbonate ions from the reaction solution. Moreover, compared with hydroxyapatite crystals coated on the enamel when synthesized by a one-step method, the CaCO3 coating that was synthesized in the first step acted as an active bridge layer and sacrificial template. It played a vital role in orienting the artificial coating layer through the template effect. The results show that the rod-like carbonated hydroxyapatite crystals grow into bundles, which are similar in size and appearance to prisms in human enamel, when using the two-step method with either aspartic acid or acidic glutamate (20.00 mmol/L). PMID:26046278

  6. 40 CFR 70.12 - Enforceable commitments for further actions addressing greenhouse gases (GHGs).

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ... actions addressing greenhouse gases (GHGs). 70.12 Section 70.12 Protection of Environment ENVIRONMENTAL... commitments for further actions addressing greenhouse gases (GHGs). (a) Definitions. (1) Greenhouse Gases... six greenhouse gases: carbon dioxide, nitrous oxide, methane, hydrofluorocarbons,...

  7. 40 CFR 70.12 - Enforceable commitments for further actions addressing greenhouse gases (GHGs).

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ... actions addressing greenhouse gases (GHGs). 70.12 Section 70.12 Protection of Environment ENVIRONMENTAL... commitments for further actions addressing greenhouse gases (GHGs). (a) Definitions. (1) Greenhouse Gases... six greenhouse gases: carbon dioxide, nitrous oxide, methane, hydrofluorocarbons,...

  8. 40 CFR 70.12 - Enforceable commitments for further actions addressing greenhouse gases (GHGs).

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ... actions addressing greenhouse gases (GHGs). 70.12 Section 70.12 Protection of Environment ENVIRONMENTAL... commitments for further actions addressing greenhouse gases (GHGs). (a) Definitions. (1) Greenhouse Gases... six greenhouse gases: carbon dioxide, nitrous oxide, methane, hydrofluorocarbons,...

  9. 40 CFR 70.12 - Enforceable commitments for further actions addressing greenhouse gases (GHGs).

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... actions addressing greenhouse gases (GHGs). 70.12 Section 70.12 Protection of Environment ENVIRONMENTAL... commitments for further actions addressing greenhouse gases (GHGs). (a) Definitions. (1) Greenhouse Gases... six greenhouse gases: carbon dioxide, nitrous oxide, methane, hydrofluorocarbons,...

  10. 40 CFR 70.12 - Enforceable commitments for further actions addressing greenhouse gases (GHGs).

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ... actions addressing greenhouse gases (GHGs). 70.12 Section 70.12 Protection of Environment ENVIRONMENTAL... commitments for further actions addressing greenhouse gases (GHGs). (a) Definitions. (1) Greenhouse Gases... six greenhouse gases: carbon dioxide, nitrous oxide, methane, hydrofluorocarbons,...

  11. Hydrophobic Catalysts For Removal Of NOx From Flue Gases

    NASA Technical Reports Server (NTRS)

    Sharma, Pramod K.; Hickey, Gregory S.; Voecks, Gerald E.

    1995-01-01

    Improved catalysts for removal of nitrogen oxides (NO and NO2) from combustion flue gases formulated as composites of vanadium pentoxide in carbon molecular sieves. Promotes highly efficient selective catalytic reduction of NOx at relatively low temperatures while not being adversely affected by presence of water vapor and sulfur oxide gases in flue gas. Apparatus utilizing catalyst of this type easily integrated into exhaust stream of power plant to remove nitrogen oxides, generated in combustion of fossil fuels and contribute to formation of acid rain and photochemical smog.

  12. Cleaning of exhaust gases in the mold core industry

    SciTech Connect

    Balabanov, V.P.

    1988-05-01

    Methods for detoxifying the exhaust gases in the core-making sections of the casting industry were studied. The gases generated when making cores from sand-resin mixtures based on oil-free binders and synthetic resins were evaluated. Tests were conducted on activated carbon AR-3, catalysts containing precious and nonprecious metals, and on solutions of sulfuric acid, hydrogen peroxide, and sodium hypochlorate. The absorption, adsorption, and catalytic methods of cleaning the gas discharges from toxic substances were comparatively assessed. Results show that sorption methods were unsuitable while catalytic methods achieved near-total detoxification.

  13. Separation of gases through gas enrichment membrane composites

    DOEpatents

    Swedo, R.J.; Kurek, P.R.

    1988-07-19

    Thin film composite membranes having as a permselective layer a film of a homopolymer of certain vinyl alkyl ethers are useful in the separation of various gases. Such homopolymers have a molecular weight of greater than 30,000 and the alkyl group of the vinyl alkyl monomer has from 4 to 20 carbon atoms with branching within the alkyl moiety at least at the carbon atom bonded to the ether oxygen or at the next adjacent carbon atom. These membranes show excellent hydrolytic stability, especially in the presence of acidic or basic gaseous components.

  14. Separation of gases through gas enrichment membrane composites

    DOEpatents

    Swedo, Raymond J. (Mt. Prospect, IL); Kurek, Paul R. (Schaumburg, IL)

    1988-01-01

    Thin film composite membranes having as a permselective layer a film of a homopolymer of certain vinyl alkyl ethers are useful in the separation of various gases. Such homopolymers have a molecular weight of greater than 30,000 and the alkyl group of the vinyl alkyl monomer has from 4 to 20 carbon atoms with branching within the alkyl moiety at least at the carbon atom bonded to the ether oxygen or at the next adjacent carbon atom. These membranes show excellent hydrolytic stability, especially in the presence of acidic or basic gaseous components.

  15. Biofilters remove VOCs from stack gases

    SciTech Connect

    Not Available

    1993-10-01

    Weyerhaeuser's strandboard plant in Grayling, Mich., is using biofiltration to remove volatile organic compounds (VOCs) at the site. Primary constituents in the Weyerhaeuser stack gases are alcohols, aldehydes, organic acids, benzene and toluene. The alternative to biofiltration is incineration, but because the concentration of VOCs in the stack gases is so dilute, natural gas would be required. Incineration would be costly, and could introduce pollution problems by generating excess carbon dioxide (CO[sub 2]) and possibly nitrogen oxides. Two pilot biofilters, each about 20ft by 100ft in area, with 4-ft thick media of bark and ground trim ends, are using naturally occurring bacteria to destroy VOCs emanating from a wood panel press and a wood flake dryer. The press offgas biofilter, activated February 1993, had risen to 93% efficiency in removing VOCs by mid-May. The flake dryer exhaust biofilter, placed in service in April, already was more than 80% efficient.

  16. Rhodium-catalyzed hydrogenation of carbon dioxide to formic acid

    SciTech Connect

    Tsai, Jing-Cherng; Nicholas, K.M.

    1992-06-17

    The complex [Rh(NBD)(PMe{sub 2}Ph){sub 3}]BF{sub 4} (2; NBD = norbornadiene) has been found to serve as a precatalyst for the hydrogenation of carbon dioxide to formic acid at moderate temperatures in THF solution, with turnover numbers of 10-60/day. Water accelerates formic acid production, whereas PMe{sub 2}Ph is an inhibitor. Kinetic studies show that the rate of formic acid appearance in first order each in [2], pH{sub 2}, and p{sub CO2} in the range 50-300 psi (following prehydrogenation). In situ high-pressure IR and NMR experiments reveal that the addition of H{sub 2} to [Rh(NBD)(PMe{sub 2}Ph){sub 3}]BF{sub 4} (2) produces rhodium dihydride complexes [H{sub 2}Rh(PMe{sub 2}Ph){sub 3}(S)]BF{sub 4}(4, 5; S = H{sub 2}O, THF) and [H{sub 2}Rh(PMe{sub 2}Ph){sub 4}]BF{sub 4} (3). IR and NMR studies of the reaction of 3-5 with CO{sub 2} indicate that 3 is unreactive toward CO{sub 2} but that 4 and 5 insert CO{sub 2} to give species 6 and 7, formulated as formato complexes [HRh(S)(PMe{sub 2}Ph){sub 2}({eta}{sup 2}-OCHO)]BF{sub 4}, respectively; complexes 6 and 7 are also detected under catalytic conditions by IR spectroscopy. Aquo dihydride complex 4 has been found to insert CO{sub 2} more rapidly than the THF complex 5. [H{sub 2}Rh(PMe{sub 2}Ph){sub 3}(S)]BF{sub 4} (4, 5) also catalyze the decomposition of formic acid to CO{sub 2} and H{sub 2}. Combined kinetic and spectroscopic results suggest that reductive elimination of formic acid from the intermediate formato complexes is the rate-limiting step in the catalytic cycle. 30 refs., 11 figs., 1 tab.

  17. Carbon Dioxide Information Analysis Center and World Data Center - A for atmospheric trace gases. Fiscal year 1996, annual report

    SciTech Connect

    Cushman, R.M.; Boden, T.A.; Jones, S.B.

    1997-02-01

    Fiscal year 1996 was especially productive for the Carbon Dioxide Information Analysis Center (CDIAC) at Oak Ridge National Laboratory (ORNL). This report describes publications and statistical data from the CDIAC.

  18. Toxicity of pyrolysis gases from polypropylene

    NASA Technical Reports Server (NTRS)

    Hilado, C. J.; Schneider, J. E.; Brauer, D. F.

    1979-01-01

    A sample of polypropylene was evaluated for toxicity of pyrolysis gases, using the toxicity screening test method developed at the University of San Francisco. The gases from this sample appeared to be equivalent or less toxic than the gases from a sample of polyethylene under these particular test conditions. Carbon monoxide appeared to be the principal toxicant.

  19. USE OF STABLE CARBON ISOTOPE RATIOS OF FATTY ACIDS TO EVALUATE MICROBIAL CARBON SOURCES IN TERRESTRIAL ENVIRONMENTS

    EPA Science Inventory

    We use measurements of the concentration and stable carbon isotopic ratio (D 13C) of individual microbial phospholipid fatty acids (PLFAs) in soils as indicators of live microbial biomass levels and microbial carbon source. We found that intensive sugar cane cultivation leads to ...

  20. USE OF THE COMPOSITION AND STABLE CARBON ISOTOPE RATIO OF MICROBIAL FATTY ACIDS TO STUDY CARBON CYCLING

    EPA Science Inventory

    We use measurements of the concentration and stable carbon isotopic ratio (Gamma 13C) of individual microbial phospholipid fatty acids (PLFAS) in soils and sediments as indicators of live microbial biomass levels and microbial carbon source. For studies of soil organic matter (SO...

  1. Electrochemical formation of hydroxide for enhancing carbon dioxide and acid gas uptake by a solution

    SciTech Connect

    Rau, Gregory Hudson

    2014-07-01

    A system for forming metal hydroxide from a metal carbonate utilizes a water electrolysis cell having an acid-producing anode and a hydroxyl-producing cathode immersed in a water solution of sufficient ionic content to allow an electric current to pass between the hydroxyl-producing cathode and the acid-producing anode. A metal carbonate is placed in close proximity to the acid-producing anode. A direct current electrical voltage is provided across the acid-producing anode and the hydroxyl-producing cathode sufficient to generate acid at the acid-producing anode and hydroxyl ions at the hydroxyl-producing cathode. The acid dissolves at least part of the metal carbonate into metal and carbonate ions allowing the metal ions to travel toward the hydroxyl-producing cathode and to combine with the hydroxyl ions to form the metal hydroxide. The carbonate ions travel toward the acid-producing anode and form carbonic acid and/or water and carbon dioxide.

  2. Measurement of fossil fuel carbon dioxide and other anthropogenic trace gases from MEGAPOLI intensive campaign in Paris during winter 2010

    NASA Astrophysics Data System (ADS)

    Lopez, M.; Schmidt, M.; Delmotte, M.; Gros, V.; Mondelain, D.; Lehman, S.; Ramonet, M.; Vuillemin, C.; Xueref-remy, I. C.

    2012-12-01

    The Paris agglomeration is the third biggest megacity in Europe (12 million inhabitants) and according to national emission inventories, is responsible for 15 % of the French anthropogenic CO2 emissions mainly originating from road transport, residential and industrial energy consumption. The objective of our feasibility study was to design an efficient monitoring strategy in order to quantify future trends in anthropogenic CO2 emission in Paris area. During the winter campaign of the European project MEGAPOLI and French project CO2-MEGAPARIS, we performed measurements of CO2 and related trace gases from January to February 2010. The RAMCES (Atmospheric Network for Greenhouse Gases Monitoring) team at LSCE monitored CO2 and CO mixing ratio with high temporal resolution using instruments based on Cavity Ring Down Spectroscopy (CRDS) in the thirteenth arrondissement of Paris (south). We also sampled air in more than fifty flasks covering three full days at the same place. Flasks were analysed in the RAMCES central laboratory with a Gas Chromatograph system for CO2, CO, CH4, N2O, SF6 and H2 mixing ratios and also by Mass Spectroscopy for CO2 isotopic ratios (?13C and ?18O). In order to quantify the fossil fuel CO2 (CO2ff) most flasks were analysed at INSTAAR for ?14C in CO2. In addition, 13CO2 isotopic ratio and total CO2 concentration were measured at high temporal resolution (< 1 min) over three days at Paris with Tunable Diode Laser Spectroscope developed at LPMAA. In parallel with the Paris measurements, in-situ CO2, CO and other trace gases were monitored at Gif-sur-Yvette, a semi urban station 20km south west of Paris. Similar synoptic variations of CO2 and CO mixing ratios were found in Paris and Gif with maximum mixing ratio up to 495 ppm CO2 and 1000 ppb CO downtown Paris. The mean diurnal variation during this winter period shows peak to peak amplitude of 15 ppm CO2 and 150 ppb CO at Paris and 10 ppm CO2 and 40 CO ppb at Gif station. We focused on CO and NOx as tracer of fossil fuel emission to estimate CO2ff. We calibrated these tracers against CO2ff estimates based on ?14C. Moreover, ?13C measurements were used to quantify the contribution of the different combustion sources for CO2 emission. Finally, we compared our results to the emission inventories from EDGAR 4.2 (global inventories), IER (European inventory) and the national ones from CITEPA and AirParif.

  3. Field enhancements of packed-bed performance for low-concentration acidic and basic-waste gases from semiconductor manufacturing process.

    PubMed

    Chein, Hung Min; Aggarwal, Shankar Gopala; Wu, Hsin Hsien; Chen, Tzu Ming; Huang, Chun-Chao

    2005-05-01

    Low-concentration acidic and basic-waste gas pollutants contribute significantly in the total emission of a facility. Previous results show that the control of high volumetric flow rate (approximately 500 m3/min), low-concentration acidic (< 1 ppm by vol) and basic (< 3 ppm by vol) gases from semiconductor process vent, by conventional wet scrubbing technique is a challenging task. This work was targeted to enhance the performance of packed beds for high-volumetric flow rate, low-concentration acidic (HF, HCl), and basic (NH3)-waste gases from the semiconductor manufacturing process. The methodology used to meet the goal was the application of fine-water mist over the inlet stream before entering to the packed bed and use of the surfactant with mist/packed-bed liquid in low concentration. An experimental study was carried out in two acid-packed beds to optimize the operating conditions, such as pH of the liquid, circulating liquid flow rate, blow-down cycle, and so forth. The relationship among liquid pH, liquid ionic concentration, and the removal efficiency of the packed bed for the pollutants has been discussed considering chemical equilibrium, two-film theory, and Henry's law. For the potential utilization of scrubbing water, the dependency of the efficiency on blow-down cycle was studied, and a mechanism is suggested. The proposed water-mist surfactant system was installed in two acid-packed beds, and performance of the packed beds was compared. The background efficiencies of the acid-packed beds for HF, HCl, and NH3 were found max to be (n = 11) 53, 40, and 27%, whereas after installation of the system, they increased significantly and became 76 +/- 13% (n = 10), 76 +/- 8% (n = 7), and 78 +/- 7% (n = 7), respectively, for inlet concentrations of HF and HCl < 1 ppm and NH3 < 14 ppm. The mechanism by which the surfactants operate to enhance the removal in scrubbing process is suggested considering the hydrodynamic effect and the interfacial effect with the charge-generating characteristic of surfactants on water surface, when dissolved into water. The results show that a proposed rectification system can effectively reduce the emission rates below the regulatory level (0.6 kg/hr) at the present conditions of the facility. PMID:15991673

  4. Fate of microbial nitrogen, carbon, hydrolysable amino acids, monosaccharides, and fatty acids in sediment

    NASA Astrophysics Data System (ADS)

    Veuger, Bart; van Oevelen, Dick; Middelburg, Jack J.

    2012-04-01

    The fate of microbial carbon, nitrogen, hydrolysable amino acids (HAAs), monosaccharides, and fatty acids in sediment was investigated experimentally. The microbial community of a tidal flat sediment was labeled with 13C-enriched glucose and 15N-enriched ammonium, and sediment was incubated for up to 371 days. Analysis of total concentrations and 13C- and 15N content of bulk sediment, hydrolysable amino acids (including D-alanine), monosaccharides, total fatty acids (TFAs), and phospholipid-derived fatty acids (PLFAs) allowed us to trace the fate of microbial biomass and -detritus and the major biochemical groups therein (proteins, carbohydrates, and lipids) over intermediate time scales (weeks-months). Moreover, the unidentified fraction of the labeled material (i.e. not analyzed as HAA, FA, or carbohydrate) provided information on the formation and fate of molecularly uncharacterizable organic matter. Loss of 13C and 15N from the sediment was slow (half live of 433 days) which may have been due to the permanently anoxic conditions in the experiment. Loss rates for the different biochemical groups were also low with the following order of loss rate constants: PLFA > TFA > HAA > monosaccharides. The unidentified 13C-pool was rapidly formed (within days) and then decreased relatively slowly, resulting in a gradual relative accumulation of this pool over time. Degradation and microbial reworking of the labeled material resulted in subtle, yet consistent, diagenetic changes within the different biochemical groups. In the HAA pool, glycine, lysine, and proline were lost relatively slowly (i.e. best preserved) while there was no accumulation of D-alanine relative to L-alanine, indicating no relative accumulation of bacterial macromolecules rich in D-alanine. In the fatty acid pool, there was very little difference between PLFAs and TFAs, indicating a very similar lability of these pools. Differences between individual fatty acids included a relatively slow loss of i15:0, ai15:0 and 18:1?7c which likely resulted from production of these bacterial fatty acids during bacterial reworking of the organic matter. Differences between loss rate constants for individual monosaccharides were not significant. An exception was ribose that was produced and lost relatively rapidly, which may be related to ribose being an important component of RNA. Losses of bulk 13C and 15N were closely coupled despite partly being present in different biochemicals and partly being derived from different microbial sources, indicating no selective preservation of either C or N during organic matter diagenesis.

  5. Mechanistic insight into the formation of acetic acid from the direct conversion of methane and carbon dioxide on zinc-modified H-ZSM-5 zeolite.

    PubMed

    Wu, Jian-Feng; Yu, Si-Min; Wang, Wei David; Fan, Yan-Xin; Bai, Shi; Zhang, Chuan-Wei; Gao, Qiang; Huang, Jun; Wang, Wei

    2013-09-11

    Methane and carbon dioxide are known greenhouse gases, and the conversion of these two C1-building blocks into useful fuels and chemicals is a subject of great importance. By solid-state NMR spectroscopy, we found that methane and carbon dioxide can be co-converted on a zinc-modified H-ZSM-5 zeolite (denoted as Zn/H-ZSM-5) to form acetic acid at a low temperature range of 523-773 K. Solid-state (13)C and (1)H MAS NMR investigation indicates that the unique nature of the bifunctional Zn/H-ZSM-5 catalyst is responsible for this highly selective transformation. The zinc sites efficiently activate CH4 to form zinc methyl species (-Zn-CH3), the Zn-C bond of which is further subject to the CO2 insertion to produce surface acetate species (-Zn-OOCCH3). Moreover, the Brnsted acid sites play an important role for the final formation of acetic acid by the proton transfer to the surface acetate species. The results disclosed herein may offer the new possibility for the efficient activation and selective transformation of methane at low temperatures through the co-conversion strategy. Also, the mechanistic understanding of this process will help to the rational design of robust catalytic systems for the practical conversion of greenhouse gases into useful chemicals. PMID:23981101

  6. Sorption of perfluorooctanoic acid, perfluorooctane sulfonate and perfluoroheptanoic acid on granular activated carbon.

    PubMed

    Zhang, Di; Luo, Qi; Gao, Bin; Chiang, Sheau-Yun Dora; Woodward, David; Huang, Qingguo

    2016-02-01

    The sorption of perfluorooctane sulfonate (PFOS), perfluorooctanoic acid (PFOA), and perfluoroheptanoic acid (PFHpA) on granular activated carbon (GAC) was characterized and compared to explore the underlying mechanisms. Sorption of the three perfluoroalkyl acids (PFAAs) on GAC appeared to be a rapid intra-particle diffusion process, which were well represented by the pseudo-second-order rate model with the sorption rate following the order PFOS > PFOA > PFHpA. Sorption isotherm data were well fitted by the Freundlich model with the sorption capacity (Kf) of PFOS, PFOA and PFHpA being 4.45, 2.42 and 1.66 respectively. This suggests that the hydrophilic head group on PFAAs, i.e. sulfonate vs carboxylic, has a strong influence on their sorption. Comparison between PFOA and PFHpA revealed that hydrophobicity could also play a role in the sorption of PFAAs on GAC when the fluorocarbon chain length is different. Analyses using Attenuated Total Reflection (ATR)-Fourier Transform Infrared (FTIR) spectroscopy suggested possible formation of a negative charge-assisted H-bond between PFAAs and the functionalities on GAC surfaces, including non-aromatic ketones, sulfides, and halogenated hydrocarbons. PMID:26606188

  7. Carbon Dioxide Information Analysis Center and World Data Center-A for atmospheric trace gases: Fiscal year 1995 annual report

    SciTech Connect

    Burtis, M.D.; Cushman, R.M.; Boden, T.A.; Jones, S.B.; Nelson, T.; Stoss, F.W.

    1996-01-01

    Fiscal year 1995 was both a very productive year for the Carbon Dioxide Information Analysis Center and a year of significant change. This document presents information about the most notable accomplishments made during the year. Topics include: high-lights; statistics; future plans; publications, presentations, and awards; and change in organization and staff.

  8. Fiscal Year 1998 Annual Report, Carbon Dioxide Information Analysis Center, World Data Center -- A for Atmospheric Trace Gases

    SciTech Connect

    Cushman, R.M.; Boden, T.A.; Hook, L.A.; Jones, S.B.; Kaiser, D.P.; Nelson, T.R.

    1999-03-01

    Once again, the most recent fiscal year was a productive one for the Carbon Dioxide Information Analysis Center (CDIAC) at Oak Ridge National Laboratory (ORNL), as well as a year for change. The FY 1998 in Review section in this report summarizes quite a few new and updated data and information products, and the ''What's Coming in FY 1999'' section describes our plans for this new fiscal year. During FY 1998, CDIAC began a data-management system for AmeriFlux, a long-term study of carbon fluxes between the terrestrial biosphere of the Western Hemisphere and the atmosphere. The specific objectives of AmeriFlux are to establish an infrastructure for guiding, collecting, synthesizing, and disseminating long-term measurements of CO{sub 2}, water, and energy exchange from a variety of ecosystems; collect critical new information to help define the current global CO{sub 2} budget; enable improved predictions of future concentrations of atmospheric CO{sub 2}; and enhance understanding of carbon fluxes. Net Ecosystem Production (NEP), and carbon sequestration in the terrestrial biosphere. The data-management system, available from CDIAC'S AmeriFlux home page (http://cdiac.esd.ornl.gov/programs/ameriflux/ ) is intended to provide consistent, quality-assured, and documented data across all AmeriFlux sites in the US, Canada, Costa Rica, and Brazil. It is being developed by Antoinette Brenkert and Tom Boden, with assistance from Susan Holladay (who joined CDIAC specifically to support the AmeriFlux data-management effort).

  9. Cyclic carbonation calcination studies of limestone and dolomite for CO{sub 2} separation from combustion flue gases - article no. 011801

    SciTech Connect

    Senthoorselvan, S.; Gleis, S.; Hartmut, S.; Yrjas, P.; Hupa, M.

    2009-01-15

    Naturally occurring limestone and dolomite samples, originating from different geographical locations, were tested as potential sorbents for carbonation/calcination based CO{sub 2} capture from combustion flue gases. Samples have been studied in a thermogravimetric analyzer under simulated flue gas conditions at three calcination temperatures, viz., 750{sup o}C, 875{sup o}C, and 930{sup o}C for four carbonation calcination reaction (CCR) cycles. The dolomite sample exhibited the highest rate of carbonation than the tested limestones. At the third cycle, its CO{sub 2} capture capacity per kilogram of the sample was nearly equal to that of Gotland, the highest reacting limestone tested. At the fourth cycle it surpassed Gotland, despite the fact that the CaCO{sub 3} content of the Sibbo dolomite was only 2/3 of that of the Gotland. Decay coefficients were calculated by a curve fitting exercise and its value is lowest for the Sibbo dolomite. That means, most probably its capture capacity per kilogram of the sample would remain higher well beyond the fourth cycle. There was a strong correlation between the calcination temperature, the specific surface area of the calcined samples, and the degree of carbonation. It was observed that the higher the calcination temperature, the lower the sorbent reactivity. For a given limestone/dolomite sample, sorbents CO{sub 2} capture capacity depended on the number of CCR cycles and the calcination temperature. According to the equilibrium thermodynamics, the CO{sub 2} partial pressure in the calciner should be lowered to lower the calcination temperature. This can be achieved by additional steam supply into the calciner. Steam could then be condensed in an external condenser to single out the CO{sub 2} stream from the exit gas mixture of the calciner. A calciner design based on this concept is illustrated.

  10. Evaluation of Hemostatic Effects of Carbonized Hair-Loaded Poly(L-Lactic) Acid Nanofabrics.

    PubMed

    Zhu, Yuanyuan; Qiu, Yan; Liao, Lianming

    2015-06-01

    Carbonized human hair is used to stop bleeding in traditional Chinese medicine. The present study was aimed to prepare a novel nanofiber containing carbonized human hair and evaluate its hemostatic effect. Carbonized human hair-loaded poly(L-lactic) acid nanofiber was prepared by electrospinning. The hemostatic efficacies of dressings composed of either carbonized human hair, carbonized human hair-loaded poly(L-lactic) acid nanofiber, Yunnan White Drug power or poly(L-lactic) acid nanofiber were investigated in several swine arterial and venous bleeding models. Blood loss and bleeding time were measured. In vitro, carbonized human hair, carbonized human hair-loaded nanofiber and Yunnan White Drug Powder significantly shortened the clotting time in comparison with the nanofiber control group. The hemostatic effects of the carbonized human hair-load nanofiber on liver and spleen traumatic wounds were better than those of carbonized human hair and Yunnan White Drug Powder in terms of blood loss and bleeding time. Similar effects were observed in swine femoral artery wound model. In the swine femoral vein wound model, bleeding could not be stopped in the control animals. In the carbonized human hair group, Yunnan White Drug Powder group and carbonized human hair-load nanofiber group, bleeding was stopped in 83.3%, 83.3% and 100% of the animals, respectively. In conclusion, dressing using carbonized human hair-load nanofibers is effective in controlling severe, uncontrolled bleeding. This dressing may offer a cheap alternative to dressings composed of coagulation proteins. PMID:26369029

  11. Toxic gases.

    PubMed Central

    Matthews, G.

    1989-01-01

    An overview of the widespread use of gases and some volatile solvents in modern society is given. The usual circumstances in which undue exposure may occur are described. The most prominent symptoms and general principles of diagnosis and treatment are given and are followed by more specific information on the commoner, more toxic materials. While acute poisonings constitute the greater part of the paper, some indication of chronic disorders arising from repeated or prolonged exposure is also given. PMID:2687827

  12. Studies of the terrestrial O{sub 2} and carbon cycles in sand dune gases and in biosphere 2

    SciTech Connect

    Severinghaus, J.P.

    1995-12-31

    Molecular oxygen in the atmosphere is coupled tightly to the terrestrial carbon cycle by the processes of photosynthesis, respiration, and burning. This dissertation examines different aspects of this coupling in four chapters. Chapter 1 explores the feasibility of using air from sand dunes to reconstruct atmospheric O{sub 2} composition centuries ago. Such a record would reveal changes in the mass of the terrestrial biosphere, after correction for known fossil fuel combustion, and constrain the fate of anthropogenic CO{sub 2}.

  13. Carbon Dioxide Analysis Center and World Data Center-A for Atmospheric Trace Gases fiscal year 1997 annual report

    SciTech Connect

    Burtis, M.D.; Cushman, R.M.; Boden, T.A.; Jones, S.B.; Kaiser, D.P.; Nelson, T.R.

    1998-03-01

    Fiscal year (FY) 1997 was another exciting and productive one for the Carbon Dioxide Information Analysis Center (CDIAC) at the Oak Ridge National Laboratory. During FY 1997, CDIAC launched the Quality Systems Science Center for the North American Research Strategy for Tropospheric Ozone (NARSTO). The purpose of NARSTO--a US-Canada-Mexico initiative of government agencies, industry, and the academic research community--is to improve the understanding of the formation and transport of tropospheric ozone.

  14. Using carbon and water isotopes and noble gases to assess the origin of methane in fresh water aquifers in the south of the Netherlands

    NASA Astrophysics Data System (ADS)

    Broers, Hans Peter; de Weert, Jasperien; Vonhof, Hubert; Janssen, Renee; Sueltenfuss, Juergen; Aeschbach-Hertig, Werner; Castelijns, Jeroen

    2015-04-01

    Groundwater in the Dutch subsurface is known to contain substantial concentrations of methane of which the origin is not always clear. The Dutch subsurface contains relatively high organic matter contents which makes a biogenic origin plausible, however few studies have used water and carbon isotopes to deduce the origin of methane. In relation to possible future exploitation of deep shale gas resources, it is now considered important to assess base line quality of fresh groundwater in overlying aquifers from which drinking water is produced. Therefore, we sampled the raw water of 41 large public supply well fields in the south of the Netherlands which represents a mixture of groundwater of different ages and used the a discrete travel time distribution model (DTTDM, Visser et al. 2013, WRR) in order to quantify the age distribution of the mixture. Measurements included major ion chemistry, 3H, 3He, 4He, 18O, 2H, 14C, 13C-DIC and 13C-CH4 and the full range of noble gases. 13C-CH4 measurements were carried out using a Picarro G2201-i CRDS analyser. The heavier noble gases enable the calculation of the Noble Gas Temperature (NGT) which characterizes the temperature of past recharge conditions. The 14C apparent age of each mixture was derived correcting for dead carbon sources and included carbonate dissolution and methanogenesis as the defining processes. The 13C-CH4 measurements showed a range of δ-values between -70 and -100‰, which give a clear indication for biogenic methane. No clear relations between 13C-CH4 and 13C-DIC or the 4He/CH4 ratio were observed. However, clear spatial patterns indicated that more depleted values are grouped in specific areas. The 13δCH4 values did not show a clear relation with the age distribution of the pumped water, even though a large range of age distributions was observed including old water with an age of > 25 k yrs. We believe that spatial differences in organic matter contents, origin of the geological deposits and/or the methanogenesis process itself determine the methane isotope ratios in this part of the Netherlands.

  15. Teacher's Resource Book for Balloons and Gases. Grade 6. Revised. Anchorage School District Elementary Science Program.

    ERIC Educational Resources Information Center

    Anchorage School District, AK.

    This resource book introduces sixth-grade children to the physical and chemical properties of gases. The unit begins with an investigation of acids and bases. Students then generate carbon dioxide, oxygen, and hydrogen, and investigate the properties of each. The unit culminates with an activity involving an unknown gas. Students conduct tests to…

  16. Teacher's Resource Book for Balloons and Gases. Grade 6. Revised. Anchorage School District Elementary Science Program.

    ERIC Educational Resources Information Center

    Anchorage School District, AK.

    This resource book introduces sixth-grade children to the physical and chemical properties of gases. The unit begins with an investigation of acids and bases. Students then generate carbon dioxide, oxygen, and hydrogen, and investigate the properties of each. The unit culminates with an activity involving an unknown gas. Students conduct tests to

  17. Effect of surface acidic oxides of activated carbon on adsorption of ammonia.

    PubMed

    Huang, Chen-Chia; Li, Hong-Song; Chen, Chien-Hung

    2008-11-30

    The influence of surface acidity of activated carbon (AC) was experimentally studied on adsorption of ammonia (NH(3)). Coconut shell-based AC was modified by various acids at different concentrations. There were five different acids employed to modified AC, which included nitric acid, sulfuric acid, hydrochloric acid, phosphoric acid, and acetic acid. Acidic functional groups on the surface of ACs were determined by a Fourier transform infrared spectrograph (FTIR) and by the Boehm titration method. Specific surface area and pore volume of the ACs were measured by a nitrogen adsorption apparatus. Adsorption amounts of NH(3) onto the ACs were measured by a dynamic adsorption system at room temperature according to the principle of the ASTM standard test method. The concentration of NH(3) in the effluent stream was monitored by a gas-detecting tube technique. Experimental results showed that adsorption amounts of NH(3) on the modified ACs were all enhanced. The ammonia adsorption amounts on various activated carbons modified by different acids are in the following order: nitric acid>sulfuric acid>acetic acid approximately phosphoric acid>hydrochloric acid. It is worth to note that the breakthrough capacity of NH(3) is linearly proportional to the amount of acidic functional groups of the ACs. PMID:18403110

  18. Isotopic composition of gases from mud volcanoes

    SciTech Connect

    Valysaev, B.M.; Erokhin, V.E.; Grinchenko, Y.I.; Prokhorov, V.S.; Titkov, G.A.

    1985-09-01

    A study has been made of the isotopic composition of the carbon in methane and carbon dioxide, as well as hydrogen in the methane, in the gases of mud volcanoes, for all main mud volcano areas in the USSR. The isotopic composition of carbon and hydrogen in methane shows that the gases resemble those of oil and gas deposits, while carbon dioxide of these volcanoes has a heavier isotopic composition with a greater presence of ''ultraheavy'' carbon dioxide. By the chemical and isotopic composition of gases, Azerbaidzhan and South Sakhalin types of mud volcano gases have been identified, as well as Bulganak subtypes and Akhtala and Kobystan varieties. Correlations are seen between the isotopic composition of gases and the geological build of mud volcano areas.

  19. The Formation and Stability of Carbonic Acid on Outer Solar System Bodies

    NASA Technical Reports Server (NTRS)

    Peeters, Z.; Hudson, R. L.; Moore, M. H.; Lewis, Ariel

    2009-01-01

    The radiation chemistry, thermal stability, and vapor pressure of solid-phase carbonic acid (H2CO3) have been studied with mid-infrared spectroscopy. A new procedure for measuring this molecule's radiation stability has been used to obtain intrinsic IR band strengths and half-lives for radiolytic destruction. Results are compared to literature values. We report, for the first time, measurements of carbonic acid's vapor pressure and its heat of sublimation. We also report the first observation of a chemical reaction involving solid-phase carbonic acid. Possible applications of these findings are discussed, with an emphasis on the outer Solar System.

  20. Effect of Acid Oxidation on the Dispersion Property of Multiwalled Carbon Nanotubes

    NASA Astrophysics Data System (ADS)

    Goh, P. S.; Ismail, A. F.; Aziz, M.

    2009-06-01

    A means of dispersion of multiwalled carbon nanotube (MWCNT) via mixed acid (HNO3 and H2SO4) oxidation with different treatment durations was investigated through the solubility study of the treated carbon nanotubes in some common solvents. Fourier transformed infrared (FTIR) characterization of the reaction products revealed that the surface of MWCNTs was successfully functionalized with surface acidic groups. The acid-base titration demonstrated that the amount of surface acidic groups increased in parallel with the refluxing duration. The acid modified MWCNTs were found to be well dispersed in polar solvents, such as ethanol and water due to the presence of the hydrophilic acid functional groups on the surface of raw MWCNTs. Such chemical modification of carbon nanotube properties will pave the way towards the realistic applications in the nanotechnology world.

  1. Reevaluation of the NOAA/CMDL carbon monoxide reference scale and comparisons with CO reference gases at NASA-Langley and the Fraunhofer Institut

    SciTech Connect

    Novelli, P.C.; Collins, J.E. Jr.; Myers, R.C.; Sachse, G.W.; Scheel, H.E.

    1994-06-01

    The carbon monoxide (CO) reference scale created by the National Oceanic and Atmospheric Administration/Climate Monitoring and Diagnostics Laboratory (NOAA/CMDL) is used to quantify measurements of CO in the atmosphere, calibrate standards of other laboratories and to otherwise provide reference gases to the community measuring atmospheric CO. This reference scale was created based upon a set of primary standards prepared by gravimetric methods at CMDL and has been propagated to a set of working standards. In this paper we compare CO mixing ratios assigned to the working standards by three approaches: (1) calibration against the original gravimetric standards, (2) calibration using only working standards as the reference gas, and (3) calibration against three new gravimetric standards prepared to CMDL. The agreement between these values was typically better than 1%. The calibration histories of CMDL working standards are reviewed with respect to expected rates of CO change in the atmosphere. Using a Monte Carlo approach to simulate the effect of drifting standards on calculated mixing ratios, we conclude that the error solely associated with the maintenance of standards will limit the ability to detect small CO changes in the atmosphere. We also report results of intercalibration experiments conducted between CMDL and the Diode Laser Sensor Group (DACOM) at the NASA Langley Research Center (Hampton, Virginia), and CMDL and the Fraunhofer-Institut (Garmisch-Partenkirchen, Germany). Each laboratory calibrated several working standards for CO using their reference gases, and these results were compared to calibrations conducted by CMDL. The intercomparison of eight standards (CO concentrations between approximately 100 and approximately 165 ppb) by CMDL and NASA agreed to better than +/- 2%. (Abstract Truncated)

  2. Reevaluation of the NOAA/CMDL carbon monoxide reference scale and comparisons with CO reference gases at NASA-Langley and the Fraunhofer Institut

    NASA Technical Reports Server (NTRS)

    Novelli, P. C.; Collins, J. E., Jr.; Myers, R. C.; Sachse, G. W.; Scheel, H. E.

    1994-01-01

    The carbon monoxide (CO) reference scale created by the National Oceanic and Atmospheric Administration/Climate Monitoring and Diagnostics Laboratory (NOAA/CMDL) is used to quantify measurements of CO in the atmosphere, calibrate standards of other laboratories and to otherwise provide reference gases to the community measuring atmospheric CO. This reference scale was created based upon a set of primary standards prepared by gravimetric methods at CMDL and has been propagated to a set of working standards. In this paper we compare CO mixing ratios assigned to the working standards by three approaches: (1) calibration against the original gravimetric standards, (2) calibration using only working standards as the reference gas, and (3) calibration against three new gravimetric standards prepared to CMDL. The agreement between these values was typically better than 1%. The calibration histories of CMDL working standards are reviewed with respect to expected rates of CO change in the atmosphere. Using a Monte Carlo approach to simulate the effect of drifting standards on calculated mixing ratios, we conclude that the error solely associated with the maintenance of standards will limit the ability to detect small CO changes in the atmosphere. We also report results of intercalibration experiments conducted between CMDL and the Diode Laser Sensor Group (DACOM) at the NASA Langley Research Center (Hampton, Virginia), and CMDL and the Fraunhofer-Institut (Garmisch-Partenkirchen, Germany). Each laboratory calibrated several working standards for CO using their reference gases, and these results were compared to calibrations conducted by CMDL. The intercomparison of eight standards (CO concentrations between approximately 100 and approximately 165 ppb) by CMDL and NASA agreed to better than +/- 2%. The calibration of six standards (CO concentrations between approximately 50 and approximately 210 ppb) by CMDL and the Fraunhofer-Institut agreed to within +/- 2% for four standards, and to within +/- 5% for all six standards.

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

    NASA Astrophysics Data System (ADS)

    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.

  4. Oxidation and reduction rates for organic carbon in the Amazon mainstream tributary and floodplain, inferred from distributions of dissolved gases

    NASA Technical Reports Server (NTRS)

    Richey, Jeffrey E.; Devol, Allan H.; Wofsy, Steven C.; Victoria, Reynaldo; Riberio, Maria N. G.

    1986-01-01

    Concentrations of CO2, O2, CH4, and N2O in the Amazon River system reflect an oxidation-reduction sequence in combination with physical mixing between the floodplain and the mainstem. Concentrations of CO2 ranged from 150 microM in the Amazon mainstem to 200 to 300 microM in aerobic waters of the floodplain, and up to 1000 microM in oxygen-depleted environments. Apparent oxygen utilization (AOU) ranged from 80 to 250 microM. Methane was highly supersaturated, with concentrations ranging from 0.06 microM in the mainstem to 100 microM on the floodplain. Concentrations of N2O were slightly supersaturated in the mainstem, but were undersaturated on the floodplain. Fluxes calculated from these concentrations indicated decomposition of 1600 g C sq m y(-1) of organic carbon in Amazon floodplain waters. Analysis of relationships between CH4, O2, and CO2 concentrations indicated that approximately 50 percent of carbon mineralization on the floodplain is anaerobic, with 20 percent lost to the atmoshphere as CH4. The predominance of anaerobic metabolism leads to consumption of N2O on the flood plane. Elevated concentrations of CH4 in the mainstem probably reflect imput from the floodplain, while high levels of CO2 in the mainstem are derived from a combination of varzea drainage and in situ respiration.

  5. Morphology-dependent Electrochemical Enhancements of Porous Carbon as Sensitive Determination Platform for Ascorbic Acid, Dopamine and Uric Acid

    NASA Astrophysics Data System (ADS)

    Cheng, Qin; Ji, Liudi; Wu, Kangbing; Zhang, Weikang

    2016-02-01

    Using starch as the carbon precursor and different-sized ZnO naoparticles as the hard template, a series of porous carbon materials for electrochemical sensing were prepared. Experiments of scanning electron microscopy, transmission electron microscopy and Nitrogen adsorption-desorption isotherms reveal that the particle size of ZnO has big impacts on the porous morphology and surface area of the resulting carbon materials. Through ultrasonic dispersion of porous carbon and subsequent solvent evaporation, different sensing interfaces were constructed on the surface of glassy carbon electrode (GCE). The electrochemical behaviors of ascorbic acid (AA), dopamine (DA) and uric acid (UA) were studied. On the surface of porous carbon materials, the accumulation efficiency and electron transfer ability of AA, DA and UA are improved, and consequently their oxidation signals enhance greatly. Moreover, the interface enhancement effects of porous carbon are also controlled by the particle size of hard template. The constructed porous carbon interface displays strong signal amplification ability and holds great promise in constructing a sensitive platform for the simultaneous determination of AA, DA and UA.

  6. Morphology-dependent Electrochemical Enhancements of Porous Carbon as Sensitive Determination Platform for Ascorbic Acid, Dopamine and Uric Acid.

    PubMed

    Cheng, Qin; Ji, Liudi; Wu, Kangbing; Zhang, Weikang

    2016-01-01

    Using starch as the carbon precursor and different-sized ZnO naoparticles as the hard template, a series of porous carbon materials for electrochemical sensing were prepared. Experiments of scanning electron microscopy, transmission electron microscopy and Nitrogen adsorption-desorption isotherms reveal that the particle size of ZnO has big impacts on the porous morphology and surface area of the resulting carbon materials. Through ultrasonic dispersion of porous carbon and subsequent solvent evaporation, different sensing interfaces were constructed on the surface of glassy carbon electrode (GCE). The electrochemical behaviors of ascorbic acid (AA), dopamine (DA) and uric acid (UA) were studied. On the surface of porous carbon materials, the accumulation efficiency and electron transfer ability of AA, DA and UA are improved, and consequently their oxidation signals enhance greatly. Moreover, the interface enhancement effects of porous carbon are also controlled by the particle size of hard template. The constructed porous carbon interface displays strong signal amplification ability and holds great promise in constructing a sensitive platform for the simultaneous determination of AA, DA and UA. PMID:26924080

  7. Morphology-dependent Electrochemical Enhancements of Porous Carbon as Sensitive Determination Platform for Ascorbic Acid, Dopamine and Uric Acid

    PubMed Central

    Cheng, Qin; Ji, Liudi; Wu, Kangbing; Zhang, Weikang

    2016-01-01

    Using starch as the carbon precursor and different-sized ZnO naoparticles as the hard template, a series of porous carbon materials for electrochemical sensing were prepared. Experiments of scanning electron microscopy, transmission electron microscopy and Nitrogen adsorption-desorption isotherms reveal that the particle size of ZnO has big impacts on the porous morphology and surface area of the resulting carbon materials. Through ultrasonic dispersion of porous carbon and subsequent solvent evaporation, different sensing interfaces were constructed on the surface of glassy carbon electrode (GCE). The electrochemical behaviors of ascorbic acid (AA), dopamine (DA) and uric acid (UA) were studied. On the surface of porous carbon materials, the accumulation efficiency and electron transfer ability of AA, DA and UA are improved, and consequently their oxidation signals enhance greatly. Moreover, the interface enhancement effects of porous carbon are also controlled by the particle size of hard template. The constructed porous carbon interface displays strong signal amplification ability and holds great promise in constructing a sensitive platform for the simultaneous determination of AA, DA and UA. PMID:26924080

  8. Electron microscopy of carbonaceous matter in Allende acid residues

    NASA Technical Reports Server (NTRS)

    Lumpkin, G. R.

    1982-01-01

    On the basis of characteristic diffuse ring diffraction patterns, much of the carbonaceous matter in a large suite of Allende acid residues has been identified as a variety of turbostratic carbon. Crystallites of this phase contain randomly stacked sp(2) hybridized carbon layers and diffraction patterns resemble those from carbon black and glassy carbon. Carbynes are probably absent, and are certainly restricted to less than 0.5% of these acid residues. The work of Ott et al. (1981) provides a basis for the possibility that turbostratic carbon is a carrier of noble gases, but an additional component - amorphous carbon - may be necessary to explain the high release temperatures of noble gases as well as the glassy character of many of the carbonaceous particles. Carbynes are considered to be questionable as important carriers of noble gases in the Allende acid residues.

  9. The Orbiting Carbon Observatory (OCO-2) Mission and Experience Gained from the Greenhouse gases Observing Satellite (GOSAT)

    NASA Astrophysics Data System (ADS)

    Eldering, A.; Gunson, M.; Crisp, D.; Miller, C. E.

    2012-04-01

    The NASA Orbiting Carbon Observatory (OCO-2) will make space-based measurements of atmospheric CO2 with the precision, resolution, and coverage needed to characterize CO2 sources and sinks on regional scales and quantify their variability over the seasonal cycle. The OCO-2 mission will be a 'carbon copy' of the OCO mission, to minimize schedule and cost risks. The OCO-2 instrument has been built and is undergoing testing and characterization. OCO-2 will carry a single instrument that incorporates 3 high resolution grating spectrometers that will make bore-sighted measurements of reflected sunlight in near-infrared CO2 and molecular oxygen (O2) absorption bands. These measurements will be combined to provide spatially resolved estimates of the column-averaged CO2 dry air mole fraction, XCO2. The instrument collects 12 to 24 XCO2 soundings/second over the sunlit portion of the orbit, yielding 200 to 400 soundings per degree of latitude, or 0.5 to 1 million soundings every day. Thick clouds and aerosols will reduce the number of soundings available for XCO2 retrievals by 80-90%, but the remaining data is expected to yield XCO2 estimates with accuracies of ~0.3 to 0.5% (1 to 2 ppm) on regional scales every month. To verify the accuracy of the space-based XCO2 data, the OCO-2 validation program will use ground-based, solar-viewing Fourier Transform Spectrometers (FTS) in the Total Carbon Column Observing Network (TCCON) to tie the space-based XCO2 with the World Meteorological Organization (WMO) standard for atmospheric CO2, which is based on in situ observations of CO2 from flask measurements, tall towers, and aircraft. In preparation for the OCO-2 mission, we are using the OCO-2 algorithm to retrieve XCO2 from GOSAT measurements. We now retrieved XCO2 from GOSAT data from April 2009 to present. These retrievals are being validated with the TCCON network. This presentation will provide an overview of OCO-2 mission, including science objectives, instrument, algorithm, and validation plans as well as recent results from the GOSAT retrievals.

  10. Adsorption of organic acids from dilute aqueous solution onto activated carbon

    SciTech Connect

    Wang, S.W.

    1980-06-01

    The radioisotope technique was used to study the removal of organic acid contaminants from dilute aqueous solutions onto activated carbon. Acetic acid, propionic acid, n-butyric acid, n-hexanoic acid and n-heptanoic acid were studied at 278, 298, and 313/sup 0/K. Three bi-solute acid mixtures (acetic and propionic acids, acetic and butanoic acids, and propionic and butanoic acids) were studied at 278 and 298/sup 0/K. Isotherms of the single-solute systems were obtained at three different temperatures in the very dilute concentration region (less than 1% by weight). These data are very important in the prediction of bi-solute equilibrium data. A Polanyi-based competitive adsorption potential theory was used to predict the bi-solute equilibrium uptakes. Average errors between calculated and experimental data ranges from 4% to 14%. It was found that the competitive adsorption potential theory gives slightly better results than the ideal adsorbed solution theory.

  11. Molten Carbonate and Phosphoric Acid Stationary Fuel Cells: Overview and Gap Analysis

    SciTech Connect

    Remick, R.; Wheeler, D.

    2010-09-01

    This report describes the technical and cost gap analysis performed to identify pathways for reducing the costs of molten carbonate fuel cell (MCFC) and phosphoric acid fuel cell (PAFC) stationary fuel cell power plants.

  12. A Functional Tricarboxylic Acid Cycle Operates during Growth of Bordetella pertussis on Amino Acid Mixtures as Sole Carbon Substrates

    PubMed Central

    Garnier, Dominique; Speck, Denis

    2015-01-01

    It has been claimed that citrate synthase, aconitase and isocitrate dehydrogenase activities are non-functional in Bordetella pertussis and that this might explain why this bacterium’s growth is sometimes associated with accumulation of polyhydroxybutyrate (PHB) and/or free fatty acids. However, the sequenced genome includes the entire citric acid pathway genes. Furthermore, these genes were expressed and the corresponding enzyme activities detected at high levels for the pathway when grown on a defined medium imitating the amino acid content of complex media often used for growth of this pathogenic microorganism. In addition, no significant PHB or fatty acids could be detected. Analysis of the carbon balance and stoichiometric flux analysis based on specific rates of amino acid consumption, and estimated biomass requirements coherent with the observed growth rate, clearly indicate that a fully functional tricarboxylic acid cycle operates in contrast to previous reports. PMID:26684737

  13. A Functional Tricarboxylic Acid Cycle Operates during Growth of Bordetella pertussis on Amino Acid Mixtures as Sole Carbon Substrates.

    PubMed

    Izac, Marie; Garnier, Dominique; Speck, Denis; Lindley, Nic D

    2015-01-01

    It has been claimed that citrate synthase, aconitase and isocitrate dehydrogenase activities are non-functional in Bordetella pertussis and that this might explain why this bacterium's growth is sometimes associated with accumulation of polyhydroxybutyrate (PHB) and/or free fatty acids. However, the sequenced genome includes the entire citric acid pathway genes. Furthermore, these genes were expressed and the corresponding enzyme activities detected at high levels for the pathway when grown on a defined medium imitating the amino acid content of complex media often used for growth of this pathogenic microorganism. In addition, no significant PHB or fatty acids could be detected. Analysis of the carbon balance and stoichiometric flux analysis based on specific rates of amino acid consumption, and estimated biomass requirements coherent with the observed growth rate, clearly indicate that a fully functional tricarboxylic acid cycle operates in contrast to previous reports. PMID:26684737

  14. The use of coiled tubing during matrix acidizing of carbonate reservoirs

    SciTech Connect

    Thomas, R.L.; Milne, A.

    1995-10-01

    A laboratory and field study directed at improved well performance of horizontal wells is discussed. During the study, several wells were matrix acidized using bullhead and coiled tubing placement techniques. The study performed in carbonate reservoirs indicates acid placed with coiled tubing diverted with foam provides excellent zone coverage and damage removal. Conventional bullhead techniques do not result in effective damage removal. The study emphasizes the evaluation of the treatment results and the development of improved acidizing techniques. Laboratory simulations of matrix acidizing indicate proper placement techniques are essential. This observation is supported by field data in oil wells completed in carbonate reservoirs. The key to successful damage removal is (1) the placement of acid via coiled tubing and (2) proper diversion. Production logging and well performance data support this claim. The proposed treatment is applicable in both horizontal and vertical wells completed in carbonate reservoirs.

  15. The nature of the products of deprotonation of disulfonyl carbon acids in acetonitrile solvent

    NASA Astrophysics Data System (ADS)

    Binkowska, I.; Jarczewski, A.

    2006-09-01

    The series of bis(ethylsulfonyl) and bis(benzylsulfonyl) activated carbon acids were synthesized and the products of the deprotonation of these carbon acids by strong, organic, cyclic bases such as: 1,5,7-triazabicyclo[4.4.0]dec-5-ene (TBD) and 7-methyl-1,5,7-triazabicyclo[4.4.0]dec-5-ene (MTBD) in acetonitrile were characterized by conductance measurements. The values of p Ka in acetonitrile are in the range between 19.1 and 24.23 for disulfonyl carbon acids and 25.96 and 25.0 for TBD and MTBD appropriately. The conductometric titration of 0.001 M carbon acids solution in acetonitrile with 0.1 M TBD or 0.1 M MTBD in acetonitrile has been carried out. The dissociation constant values of the products of the reaction between studied carbon acids and TBD and MTBD bases in acetonitrile at 25 °C have been estimated. The results of the conductometric study for various disulfonyl carbon acids indicate convincingly that the products of the studied proton transfer reactions in acetonitrile occur as free ions or can exist also in the form of ion pairs in case of phenyl[bis(ethylsulfonyl)]methane.

  16. SIMULTANEOUS INHIBITION OF CARBON AND NITROGEN MINERALIZATION IN A FOREST SOIL BY SIMULATED ACID PRECIPITATION

    EPA Science Inventory

    Acid Precipitation may alter the rates of microbial processes in soil that are important for forest productivity. Acidification of soil can result in a depression of carbon mineralization. The present study was designed to determine whether the inhibition of carbon mineralization...

  17. USE OF THE COMPOSITION AND STABLE CARBONIISOTOPE RATIO OF MICROBIAL FATTY ACIDS TO STUDY CARBON CYCLING

    EPA Science Inventory

    We use measurements of the concentration and stable carbon isotopic ratio (*13C) of individual microbial phospholipid fatty acids (PLFAs) in soils and sediments as indicators of live microbial biomass levels and microbial carbon source. For studies of soil organic matter (SOM) cy...

  18. Use of molecular modeling to determine the interaction and competition of gases within coal for carbon dioxide sequestration

    SciTech Connect

    Jeffrey D. Evanseck; Jeffry D. Madura; Jonathan P. Mathews

    2006-04-21

    Molecular modeling was employed to both visualize and probe our understanding of carbon dioxide sequestration within a bituminous coal. A large-scale (>20,000 atoms) 3D molecular representation of Pocahontas No. 3 coal was generated. This model was constructed based on a the review data of Stock and Muntean, oxidation and decarboxylation data for aromatic clustersize frequency of Stock and Obeng, and the combination of Laser Desorption Mass Spectrometry data with HRTEM, enabled the inclusion of a molecular weight distribution. The model contains 21,931 atoms, with a molecular mass of 174,873 amu, and an average molecular weight of 714 amu, with 201 structural components. The structure was evaluated based on several characteristics to ensure a reasonable constitution (chemical and physical representation). The helium density of Pocahontas No. 3 coal is 1.34 g/cm{sup 3} (dmmf) and the model was 1.27 g/cm{sup 3}. The structure is microporous, with a pore volume comprising 34% of the volume as expected for a coal of this rank. The representation was used to visualize CO{sub 2}, and CH{sub 4} capacity, and the role of moisture in swelling and CO{sub 2}, and CH{sub 4} capacity reduction. Inclusion of 0.68% moisture by mass (ash-free) enabled the model to swell by 1.2% (volume). Inclusion of CO{sub 2} enabled volumetric swelling of 4%.

  19. Characteristics of ammonia, acid gases, and PM2.5 for three typical land-use types in the North China Plain.

    PubMed

    Xu, Wen; Wu, Qinghua; Liu, Xuejun; Tang, Aohan; Dore, Anthony J; Heal, Mathew R

    2016-01-01

    Air pollution is one of the most serious environmental problems in China due to its rapid economic development alongside a very large consumption of fossil fuel, particularly in the North China Plain (NCP). During the period 2011-2014, we integrated active and passive sampling methods to perform continuous measurements of NH3, HNO3, NO2, and PM2.5 at two urban, one suburban, and two rural sites in the NCP. The annual average concentrations of NH3, NO2, and HNO3 across the five sites were in the ranges 8.5-23.0, 22.2-50.5, and 5.5-9.7 μg m(-3), respectively, showing no significant spatial differences for NH3 and HNO3 but significantly higher NO2 concentration at the urban sites. At each site, annual average concentrations of NH3 and NO2 showed increasing and decreasing trends, respectively, while there was no obvious trend in annual HNO3 concentrations. Daily PM2.5 concentrations ranged from 11.8 to 621.0 μg m(-3) at the urban site, from 19.8 to 692.9 μg m(-3) at the suburban site, and from 23.9 to 754.5 μg m(-3) at the two rural sites, with more than 70 % of sampling days exceeding 75 μg m(-3). Concentrations of water-soluble ions in PM2.5 ranked differently between the non-rural and rural sites. The three dominant ions were NH4 (+), NO3 (-), and SO4 (2-) and mainly existed as (NH4)2SO4, NH4HSO4, and NH4NO3, and their concentrations averaged 48.6 ± 44.9, 41.2 ± 40.8, and 49.6 ± 35.9 μg m(-3) at the urban, suburban, and rural sites, respectively. Ion balance calculations indicated that PM2.5 was neutral at the non-rural sites but acidic at the rural sites. Seasonal variations of the gases and aerosols exhibited different patterns, depending on source emission strength and meteorological conditions. Our results suggest that a feasible pathway to control PM2.5 pollution in the NCP should target ammonia and acid gases together. PMID:26507724

  20. Carbonic Acid as a Reserve of Carbon Dioxide on Icy Moons: The Formation of Carbon Dioxide (CO2) in a Polar Environment

    NASA Astrophysics Data System (ADS)

    Jones, Brant M.; Kaiser, Ralf I.; Strazzulla, Giovanni

    2014-06-01

    Carbon dioxide (CO2) has been detected on the surface of several icy moons of Jupiter and Saturn via observation of the ?3 band with the Near-Infrared Mapping Spectrometer on board the Galileo spacecraft and the Visible-Infrared Mapping Spectrometer on board the Cassini spacecraft. Interestingly, the CO2 band for several of these moons exhibits a blueshift along with a broader profile than that seen in laboratory studies and other astrophysical environments. As such, numerous attempts have been made in order to clarify this abnormal behavior; however, it currently lacks an acceptable physical or chemical explanation. We present a rather surprising result pertaining to the synthesis of carbon dioxide in a polar environment. Here, carbonic acid was synthesized in a water (H2O)-carbon dioxide (CO2) (1:5) ice mixture exposed to ionizing radiation in the form of 5 keV electrons. The irradiated ice mixture was then annealed, producing pure carbonic acid which was then subsequently irradiated, recycling water and carbon dioxide. However, the observed carbon dioxide ?3 band matches almost exactly with that observed on Callisto; subsequent temperature program desorption studies reveal that carbon dioxide synthesized under these conditions remains in solid form until 160 K, i.e., the sublimation temperature of water. Consequently, our results suggest that carbon dioxide on Callisto as well as other icy moons is indeed complexed with water rationalizing the shift in peak frequency, broad profile, and the solid state existence on these relatively warm moons.

  1. Carbon monoxide and related trace gases and aerosols over the Amazon Basin during the wet and dry seasons

    NASA Astrophysics Data System (ADS)

    Andreae, M. O.; Artaxo, P.; Beck, V.; Bela, M.; Freitas, S.; Gerbig, C.; Longo, K.; Munger, J. W.; Wiedemann, K. T.; Wofsy, S. C.

    2012-03-01

    We present the results of airborne measurements of carbon monoxide (CO) and aerosol particle number concentration (CN) made during the Balano Atmosfrico Regional de Carbono na Amaznia (BARCA) program. The primary goal of BARCA is to address the question of basin-scale sources and sinks of CO2 and other atmospheric carbon species, a central issue of the Large-scale Biosphere-Atmosphere (LBA) program. The experiment consisted of two aircraft campaigns during November-December 2008 (BARCA-A) and May 2009 (BARCA-B), which covered the altitude range from the surface up to about 4500 m, and spanned most of the Amazon Basin. Based on meteorological analysis and measurements of the tracer, SF6, we found that airmasses over the Amazon Basin during the late dry season (BARCA-A, November 2008) originated predominantly from the Southern Hemisphere, while during the late wet season (BARCA-B, May 2009) low-level airmasses were dominated by northern-hemispheric inflow, and mid-tropospheric airmasses were of mixed origin. In BARCA-A we found strong influence of biomass burning emissions on the composition of the atmosphere over much of the Amazon Basin, with CO enhancements up to 300 ppb and CN concentrations approaching 10 000 cm-3; the highest values were in the southern part of the Basin at altitudes of 1-3 km. The ?CN/?CO ratios were diagnostic for biomass burning emissions, and were lower in aged than in fresh smoke. Fresh emissions indicated CO/CO2 and CN/CO emission ratios in good agreement with previous work, but our results also highlight the need to consider the residual smoldering combustion that takes place after the active flaming phase of deforestation fires. During the late wet season, in contrast, there was little evidence for a significant presence of biomass smoke. Low CN concentrations (300-500 cm-3) prevailed basinwide, and CO mixing ratios were enhanced by only ~10 ppb above the mixing line between Northern and Southern Hemisphere air. There was no detectable trend in CO with distance from the coast, but there was a small enhancement of CO in the boundary layer suggesting diffuse biogenic sources from photochemical degradation of biogenic volatile organic compounds or direct biological emission. Simulations of CO distributions during BARCA-A using a range of models yielded general agreement in spatial distribution and confirm the important contribution from biomass burning emissions, but the models evidence some systematic quantitative differences compared to observed CO concentrations. These mismatches appear to be related to problems with the accuracy of the global background fields, the role of vertical transport and biomass smoke injection height, the choice of model resolution, and reliability and temporal resolution of the emissions data base.

  2. Carbon monoxide and related trace gases and aerosols over the Amazon Basin during the wet and dry seasons

    NASA Astrophysics Data System (ADS)

    Andreae, M. O.; Artaxo, P.; Beck, V.; Bela, M.; Freitas, S.; Gerbig, C.; Longo, K.; Munger, J. W.; Wiedemann, K. T.; Wofsy, S. C.

    2012-07-01

    We present the results of airborne measurements of carbon monoxide (CO) and aerosol particle number concentration (CN) made during the Balano Atmosfrico Regional de Carbono na Amaznia (BARCA) program. The primary goal of BARCA is to address the question of basin-scale sources and sinks of CO2 and other atmospheric carbon species, a central issue of the Large-scale Biosphere-Atmosphere (LBA) program. The experiment consisted of two aircraft campaigns during November-December 2008 (BARCA-A) and May-June 2009 (BARCA-B), which covered the altitude range from the surface up to about 4500 m, and spanned most of the Amazon Basin. Based on meteorological analysis and measurements of the tracer, SF6, we found that airmasses over the Amazon Basin during the late dry season (BARCA-A, November 2008) originated predominantly from the Southern Hemisphere, while during the late wet season (BARCA-B, May 2009) low-level airmasses were dominated by northern-hemispheric inflow and mid-tropospheric airmasses were of mixed origin. In BARCA-A we found strong influence of biomass burning emissions on the composition of the atmosphere over much of the Amazon Basin, with CO enhancements up to 300 ppb and CN concentrations approaching 10 000 cm-3; the highest values were in the southern part of the Basin at altitudes of 1-3 km. The ?CN/?CO ratios were diagnostic for biomass burning emissions, and were lower in aged than in fresh smoke. Fresh emissions indicated CO/CO2 and CN/CO emission ratios in good agreement with previous work, but our results also highlight the need to consider the residual smoldering combustion that takes place after the active flaming phase of deforestation fires. During the late wet season, in contrast, there was little evidence for a significant presence of biomass smoke. Low CN concentrations (300-500 cm-3) prevailed basinwide, and CO mixing ratios were enhanced by only ~10 ppb above the mixing line between Northern and Southern Hemisphere air. There was no detectable trend in CO with distance from the coast, but there was a small enhancement of CO in the boundary layer suggesting diffuse biogenic sources from photochemical degradation of biogenic volatile organic compounds or direct biological emission. Simulations of CO distributions during BARCA-A using a range of models yielded general agreement in spatial distribution and confirm the important contribution from biomass burning emissions, but the models evidence some systematic quantitative differences compared to observed CO concentrations. These mismatches appear to be related to problems with the accuracy of the global background fields, the role of vertical transport and biomass smoke injection height, the choice of model resolution, and reliability and temporal resolution of the emissions data base.

  3. Inhibition of nitrobenzene adsorption by water cluster formation at acidic oxygen functional groups on activated carbon.

    PubMed

    Kato, Yuichi; Machida, Motoi; Tatsumoto, Hideki

    2008-06-15

    The inhibition effect of nitrobenzene adsorption by water clusters formed at the acidic groups on activated carbon was examined in aqueous and n-hexane solution. The activated carbon was oxidized with nitric acid to introduce CO complexes and then outgassed in helium flow at 1273 K to remove them completely without changing the structural properties of the carbon as a reference adsorbent. The amounts of acidic functional groups were determined by applying Boehm titration. A relative humidity of 95% was used to adsorb water onto the carbon surface. Strong adsorption of water onto the oxidized carbon can be observed by thermogravimetric analysis. The adsorption kinetic rate was estimated to be controlled by diffusion from the kinetic analysis. Significant decline in both capacity and kinetic rate for nitrobenzene adsorption onto the oxidized carbon was also observed in n-hexane solution by preadsorption of water to the carbon surface, whereas it was not detected for the outgassed carbons. These results might reveal that water molecules forming clusters at the CO complexes inhibited the entrance of nitrobenzene into the interparticles of the carbon. PMID:18440013

  4. USE OF MOLECULAR MODELING TO DETERMINE THE INTERACTION AND COMPETITION OF GASES WITHIN COAL FOR CARBON DIOXIDE SEQUESTRATION

    SciTech Connect

    Jeffrey D. Evanseck; Jeffry D. Madura; Jonathan P. Mathews

    2005-05-27

    We have made progress in carrying out large scale molecular dynamics simulations using the CHARMM force field in order to refine our coal/guest interactions. There have been two issues facing us over the last year. First, we have had to create a completely new topology and parameter definition for coal. Since we are using a classical force field, we have adopted the strategy of treating coal composed of individual common fragments based upon a distribution of mass, composition, and bonding. Our procedure is similar to treating a protein as being composed of the discrete set of amino acids. Second, we have had to incorporate the quality CO{sub 2} parameters that we have developed over the last two years. There are the geometric and arithmetic procedures, which we have successfully implemented. We have utilized computational molecular modeling to generate a state-of-the-art large scale structural representation of a bituminous coal of low volatile bituminous rank. This structure(s) has been used to investigate the molecular forces between the bituminous coal structure (or idealized pores) and the molecular species CH{sub 4} and CO{sub 2}. We are close to carrying out molecular dynamics simulations, which will allow us to explore and test the newly created model of coal.

  5. Carbon Isotope Compositions of Fatty Acids in Mussels from Newfoundland Estuaries

    NASA Astrophysics Data System (ADS)

    Murphy, Dena E.; Abrajano, Teofilo A.

    1994-09-01

    This paper examines the carbon isotopic compositions of free fatty acids of two species of mussels (i.e. Mytilus edulis and Modiolus modiolus) from two estuarine environments around Newfoundland. Gas chromatography and conventional isotope ratio mass spectrometry were employed to characterize bulk fatty acids and gas chromatography/combustion/isotope ratio mass spectrometry was utilized to characterize the carbon isotope compositions of individual fatty acids. The bulk fatty acid distribution (dominance of 16:0, 20:5n3, 22:6n3 and 16:1) and carbon isotopic compositions (-273 to -258 per mil) indicate a dominant marine phytoplankton dietary source for the mussels. In contrast to the narrow range of bulk fatty acid ? 13C values, up to 7 per mil variation in ? 13C of individual fatty acids was observed. In general, saturated fatty acids are isotopically heavier than corresponding mono- and polyunsaturates, consistent with previously suggested kinetic isotope effect associated with de novo desaturation reactions. The depletion of 13 C in 18:4n3 compared with 22:6n3 and 20:5n3 indicates a distinct dietary source for 18:4n3. The present study shows the potential for detailed assessment of carbon flow in benthic ecosystems using fatty acids and other compound classes by gas chromatography/combustion/isotope ratio mass spectrometry.

  6. PERFORMANCE AND MODELING OF A HOT POTASSIUM CARBONATE ACID GAS REMOVAL SYSTEM IN TREATING COAL GAS

    EPA Science Inventory

    The report discusses the performance and modeling of a hot potassium carbonate (K2CO3) acid gas removal system (AGRS) in treating coal gas. Aqueous solutions of K2CO3, with and without amine additive, were used as the acid gas removal solvent in the Coal Gasification/Gas Cleaning...

  7. Amino Acid Synthesis in a Supercritical Carbon Dioxide - Water System

    PubMed Central

    Fujioka, Kouki; Futamura, Yasuhiro; Shiohara, Tomoo; Hoshino, Akiyoshi; Kanaya, Fumihide; Manome, Yoshinobu; Yamamoto, Kenji

    2009-01-01

    Mars is a CO2-abundant planet, whereas early Earth is thought to be also CO2-abundant. In addition, water was also discovered on Mars in 2008. From the facts and theory, we assumed that soda fountains were present on both planets, and this affected amino acid synthesis. Here, using a supercritical CO2/liquid H2O (10:1) system which mimicked crust soda fountains, we demonstrate production of amino acids from hydroxylamine (nitrogen source) and keto acids (oxylic acid sources). In this research, several amino acids were detected with an amino acid analyzer. Moreover, alanine polymers were detected with LC-MS. Our research lights up a new pathway in the study of lifes origin. PMID:19582225

  8. Amino acid synthesis in a supercritical carbon dioxide - water system.

    PubMed

    Fujioka, Kouki; Futamura, Yasuhiro; Shiohara, Tomoo; Hoshino, Akiyoshi; Kanaya, Fumihide; Manome, Yoshinobu; Yamamoto, Kenji

    2009-06-01

    Mars is a CO(2)-abundant planet, whereas early Earth is thought to be also CO(2)-abundant. In addition, water was also discovered on Mars in 2008. From the facts and theory, we assumed that soda fountains were present on both planets, and this affected amino acid synthesis. Here, using a supercritical CO(2)/liquid H(2)O (10:1) system which mimicked crust soda fountains, we demonstrate production of amino acids from hydroxylamine (nitrogen source) and keto acids (oxylic acid sources). In this research, several amino acids were detected with an amino acid analyzer. Moreover, alanine polymers were detected with LC-MS. Our research lights up a new pathway in the study of life's origin. PMID:19582225

  9. Surface modification of activated carbon for enhanced adsorption of perfluoroalkyl acids from aqueous solutions.

    PubMed

    Zhi, Yue; Liu, Jinxia

    2016-02-01

    The objective of the research was to examine the effect of increasing carbon surface basicity on uptake of perfluorooctane sulfonic (PFOS) and carboxylic acids (PFOA) by activated carbon. Granular activated carbons made from coal, coconut shell, wood, and phenolic-polymer-based activated carbon fibers were modified through high-temperature and ammonia gas treatments to facilitate systematical evaluation of the impact of basicity of different origins. Comparison of adsorption isotherms and adsorption distribution coefficients showed that the ammonia gas treatment was more effective than the high-temperature treatment in enhancing surface basicity. The resultant higher point of zero charges and total basicity (measured by total HCl uptake) correlated with improved adsorption affinity for PFOS and PFOA. The effectiveness of surface modification to enhance adsorption varied with carbon raw material. Wood-based carbons and activated carbon fibers showed enhancement by one to three orders of magnitudes while other materials could experience reduction in adsorption towards either PFOS or PFOA. PMID:26469934

  10. Highly ordered three dimensional macroporous carbon spheres and their acid catalytic properties

    NASA Astrophysics Data System (ADS)

    Huang, Hui; Zhang, Jianming; Zhang, Yuxiao; Lian, Suoyuan; Liu, Yang

    2013-10-01

    Highly ordered three dimensional macroporous carbon spheres bearing sulfonic acid groups (MPCS-SO3H) were prepared by incomplete carbonization of glucose in silica crystal bead template, followed by sulfonation and removal of the template. The composition and porous structure of the obtained carbon spheres were investigated by physical adsorption of nitrogen, scanning electron microscopy, energy dispersive X-ray spectroscopy, and transmission electron microscopy techniques. While the Fourier-transform infrared spectroscopy was used to characterize the functional groups on the surface of carbon spheres. The catalytic properties of the MPCS-SO3H were evaluated by esterification of ethanol with acetic acid, indicating that MPCS-SO3H possess remarkable catalytic performance (high stability and acid catalytic ability) for the esterification.

  11. Computational and experimental studies of the interaction between single-walled carbon nanotubes and folic acid

    NASA Astrophysics Data System (ADS)

    Castillo, John J.; Rozo, Ciro E.; Castillo-Len, Jaime; Rindzevicius, Tomas; Svendsen, Winnie E.; Rozlosnik, Noemi; Boisen, Anja; Martnez, Fernando

    2013-03-01

    This Letter involved the preparation of a conjugate between single-walled carbon nanotubes and folic acid that was obtained without covalent chemical functionalization using a simple 'one pot' synthesis method. Subsequently, the conjugate was investigated by a computational hybrid method: our own N-layered Integrated Molecular Orbital and Molecular Mechanics (B3LYP(6-31G(d):UFF)). The results confirmed that the interaction occurred via hydrogen bonding between protons of the glutamic moiety from folic acid and ? electrons from the carbon nanotubes. The single-walled carbon nanotube-folic acid conjugate presented herein is believed to lead the way to new potential applications as carbon nanotube-based drug delivery systems.

  12. Photochemical functionalization of diamond films using a short carbon chain acid

    NASA Astrophysics Data System (ADS)

    Wang, Chun; Huang, Nan; Zhuang, Hao; Yang, Bing; Zhai, Zhaofeng; Jiang, Xin

    2016-02-01

    Diamond is recognized as a promising semiconductor material for biological applications, because of its high chemical stability and biocompatibility. Here, we report an acid with only three carbon chain, acrylic acid (AA), for the functionalization of H-terminated diamond film via photochemical method. The successfully modified surfaces were characterized by X-ray photoelectron spectroscopy (XPS), Fourier transform infrared (FTIR) spectroscopy and contact angle analyzer. Our functionalization approach was proven to be simple and facile, which shows a new potential opportunity for the photochemical modification of diamond surface with short carbon chain acid.

  13. X-ray microtomography of hydrochloric acid propagation in carbonate rocks.

    PubMed

    Machado, A C; Oliveira, T J L; Cruz, F B; Lopes, R T; Lima, I

    2015-02-01

    Acid treatments are used in the oil and gas industry, to increase the permeability of the carbonate reservoirs by creating preferential channels, called wormholes. Channels formation is strongly influenced by acid type and injection rate. The aim of this study is to evaluate some characteristics of the microporous system of carbonate rocks, before and after acidizing. For that purpose X-ray high-resolution microtomography was used. The results show that this technique can be used as a reliable method to analyze microstructural characteristics of the wormholes. PMID:25485884

  14. Development of poly(aspartic acid-co-malic acid) composites for calcium carbonate and sulphate scale inhibition.

    PubMed

    Mithil Kumar, N; Gupta, Sanjay Kumar; Jagadeesh, Dani; Kanny, K; Bux, F

    2015-01-01

    Polyaspartic acid (PSI) is suitable for the inhibition of inorganic scale deposition. To enhance its scale inhibition efficiency, PSI was modified by reacting aspartic acid with malic acid (MA) using thermal polycondensation polymerization. This reaction resulted in poly(aspartic acid-co-malic acid) (PSI-co-MA) dual polymer. The structural, chemical and thermal properties of the dual polymers were analysed by using scanning electron microscopy, Fourier transform infrared spectroscopy, X-ray diffraction, differential scanning calorimetry and gel permeation chromatography. The effectiveness of six different molar ratios of PSI-co-MA dual polymer for calcium carbonate and calcium sulphate scale inhibition at laboratory scale batch experiments was evaluated with synthetic brine solution at selected doses of polymer at 65-70C by the static scale test method. The performance of PSI-co-MA dual polymer for the inhibition of calcium carbonate and calcium sulphate precipitation was compared with that of a PSI single polymer. The PSI-co-MA exhibited excellent ability to control inorganic minerals, with approximately 85.36% calcium carbonate inhibition and 100% calcium sulphate inhibition at a level of 10?mg/L PSI-co-MA, respectively. Therefore, it may be reasonably concluded that PSI-co-MA is a highly effective scale inhibitor for cooling water treatment applications. PMID:25371160

  15. Dissimilation of Carbon Monoxide to Acetic Acid by Glucose-Limited Cultures of Clostridium thermoaceticum

    PubMed Central

    Martin, Douglas R.; Misra, Arun; Drake, Harold L.

    1985-01-01

    Clostridium thermoaceticum was cultivated in glucose-limited media, and the dissimilation of CO to acetic acid was evaluated. We found that cultures catalyzed the rapid dissimilation of CO to acetic acid and CO2, with the stoichiometry obtained for conversion approximating that predicted from the following reaction: 4CO + 2H2O ? CH3CO2H + 2CO2. Growing cultures formed approximately 50 mmol (3 g) of CO-derived acetic acid per liter of culture, with the rate of maximal consumption approximating 9.1 mmol of CO consumed/h per liter of culture. In contrast, resting cells were found not to dissimilate CO to acetic acid. 14CO was incorporated, with equal distribution between the carboxyl and methyl carbons of acetic acid when the initial cultivation gas phase was 100% CO, whereas 14CO2 preferentially entered the carboxyl carbon when the initial gas phase was 100% CO2. Significantly, in the presence of saturating levels of CO, 14CO2 preferentially entered the methyl carbon, whereas saturating levels of CO2 yielded 14CO-derived labeling predominantly in the carboxyl carbon. These findings are discussed in relation to the path of carbon flow to acetic acid. PMID:16346807

  16. Preparation and characterization of sulfonic acid-functionalized single-walled carbon nanotubes

    NASA Astrophysics Data System (ADS)

    Adams, Luqman; Oki, Aderemi; Grady, Tony; McWhinney, Hylton; Luo, Zhiping

    2009-02-01

    A strategy for the functionalization of single-walled carbon nanotubes is reported. The synthesis involved the conversion of fluorinated single-walled carbon nanotubes to the thiolated derivative assisted by phosphorous pentasulfide. The thiol group is then quantitatively oxidized to the sulfonic acid group. The extent of oxidation of the thiol precursor is confirmed using X-ray photoelectron spectroscopy, which proved to be immensely useful to discriminate between the -SH and -SO 3H with a chemical shift for the sulfur 2p (approx. 5 eV). The functionalized carbon nanotubes were further characterized by infrared spectroscopy, thermogravimetric analysis, and transmission electron microscopy which revealed a significant change in morphology between the fluoro carbon nanotubes, the thiol and sulfonic acid-modified carbon nanotubes.

  17. Adsorption of perfluoroalkyl acids by carbonaceous adsorbents: Effect of carbon surface chemistry.

    PubMed

    Zhi, Yue; Liu, Jinxia

    2015-07-01

    Adsorption by carbonaceous sorbents is among the most feasible processes to remove perfluorooctane sulfonic (PFOS) and carboxylic acids (PFOA) from drinking and ground waters. However, carbon surface chemistry, which has long been recognized essential for dictating performance of such sorbents, has never been considered for PFOS and PFOA adsorption. Thus, the role of surface chemistry was systematically investigated using sorbents with a wide range in precursor material, pore structure, and surface chemistry. Sorbent surface chemistry overwhelmed physical properties in controlling the extent of uptake. The adsorption affinity was positively correlated carbon surface basicity, suggesting that high acid neutralizing or anion exchange capacity was critical for substantial uptake of PFOS and PFOA. Carbon polarity or hydrophobicity had insignificant impact on the extent of adsorption. Synthetic polymer-based Ambersorb and activated carbon fibers were more effective than activated carbon made of natural materials in removing PFOS and PFOA from aqueous solutions. PMID:25827692

  18. Inhibition Effect of Dodecylamine on Carbon Steel Corrosion in Hydrochloric Acid Solution

    NASA Astrophysics Data System (ADS)

    Chen, Zhenyu; Huang, Ling; Qiu, Yubing; Guo, Xingpeng

    2012-12-01

    Dodecylamine spontaneously adsorbs on carbon steel via its polar group (-NH2) in hydrochloric acid solution. Furthermore, it forms a monolayer film on carbon steel surface. The inhibition mechanism of dodecylamine for carbon steel is geometric blocking effect. The adsorption of dodecylamine on carbon steel surface follows Arrhenius equation. The adsorption slightly increases activated energy, but greatly reduces pre-exponential factor value. Atomic force microscopy force curves indicate that at the area without adsorbed dodecylamine, no obvious adhere force occurs. At the area with adsorbed dodecylamine, however, an average 1.3 nN adhere force is observed.

  19. Fumaric acid: an overlooked form of fixed carbon in Arabidopsis and other plant species

    SciTech Connect

    Chia, D.W.; Yoder, T.J.; Reiter, W.D.; Gibson, S.I.

    2000-10-01

    Photoassimilates are used by plants for production of energy, as carbon skeletons and in transport of fixed carbon between different plant organs. Many studies have been devoted to characterizing the factors that. regulate photoassimilate concentrations in different plant species. Most studies examining photoassimilate concentrations in C{sub 3} plants have focused on analyzing starch and soluble sugars. However, work presented here demonstrates that a number of C{sub 3} plants, including the popular model organism Arabidopsis thaliana (L.) Heynh., and agriculturally important plants, such as soybean [Glycine ma (L.) Merr.], contain significant quantities of furnaric acid. In fact, furnaric acid can accumulate to levels of several mg per g fresh weight in A-abidopsis leaves, often exceeding starch and soluble sugar levels. Furnaric acid is a component of the tricarboxylic acid cycle and, like starch and soluble sugars, can be metabolized to yield energy and carbon skeletons for production of other compounds. Fumaric acid concentrations increase with plant age and light intensity in Arabidopsis leaves. Arabidopsis phloem exudates contain significant quantities of fumaric acid, raising the possibility that fumaric acid may function in carbon transport.

  20. Assessing the potential of amino acid 13C patterns as a carbon source tracer in marine sediments: effects of algal growth conditions and sedimentary diagenesis

    NASA Astrophysics Data System (ADS)

    Larsen, T.; Bach, L. T.; Salvatteci, R.; Wang, Y. V.; Andersen, N.; Ventura, M.; McCarthy, M. D.

    2015-08-01

    Burial of organic carbon in marine sediments has a profound influence in marine biogeochemical cycles and provides a sink for greenhouse gases such as CO2 and CH4. However, tracing organic carbon from primary production sources as well as its transformations in the sediment record remains challenging. Here we examine a novel but growing tool for tracing the biosynthetic origin of amino acid carbon skeletons, based on naturally occurring stable carbon isotope patterns in individual amino acids (δ13CAA). We focus on two important aspects for δ13CAA utility in sedimentary paleoarchives: first, the fidelity of source diagnostic of algal δ13CAA patterns across different oceanographic growth conditions, and second, the ability of δ13CAA patterns to record the degree of subsequent microbial amino acid synthesis after sedimentary burial. Using the marine diatom Thalassiosira weissflogii, we tested under controlled conditions how δ13CAA patterns respond to changing environmental conditions, including light, salinity, temperature, and pH. Our findings show that while differing oceanic growth conditions can change macromolecular cellular composition, δ13CAA isotopic patterns remain largely invariant. These results emphasize that δ13CAA patterns should accurately record biosynthetic sources across widely disparate oceanographic conditions. We also explored how δ13CAA patterns change as a function of age, total nitrogen and organic carbon content after burial, in a marine sediment core from a coastal upwelling area off Peru. Based on the four most informative amino acids for distinguishing between diatom and bacterial sources (i.e., isoleucine, lysine, leucine and tyrosine), bacterially derived amino acids ranged from 10 to 15 % in the sediment layers from the last 5000 years, and up to 35 % during the last glacial period. The greater bacterial contributions in older sediments indicate that bacterial activity and amino acid resynthesis progressed, approximately as a function of sediment age, to a substantially larger degree than suggested by changes in total organic nitrogen and carbon content. It is uncertain whether archaea may have contributed to sedimentary δ13CAA patterns we observe, and controlled culturing studies will be needed to investigate whether δ13CAA patterns can differentiate bacterial from archeal sources. Further research efforts are also needed to understand how closely δ13CAA patterns derived from hydrolyzable amino acids represent total sedimentary proteineincous material, and more broadly sedimentary organic nitrogen. Overall, however, both our culturing and sediment studies suggest that δ13CAA patterns in sediments will represent a novel proxy for understanding both primary production sources, and the direct bacterial role in the ultimate preservation of sedimentary organic matter.

  1. Thermal infrared nadir observations of 24 atmospheric gases

    NASA Astrophysics Data System (ADS)

    Clarisse, Lieven; R'Honi, Yasmina; Coheur, Pierre-Franois; Hurtmans, Daniel; Clerbaux, Cathy

    2011-05-01

    Thermal infrared nadir sounders are ideal for observing total columns or vertical profiles of atmospheric gases such as water, carbon dioxide and ozone. High resolution sounders with a spectral resolution below 5 cm-1 can distinguish fine spectral features of trace gases. Forty years after the launch of the first hyperspectral sounder IRIS, we have now several state of the art instruments in orbit, with improved instrumental specifications. In this letter we give an overview of the trace gases which have been observed by infrared nadir sounders, focusing on new observations of the Infrared Atmospheric Sounding Interferometer (IASI). We present typical observations of 14 rare reactive trace gas species. Several species are reported here for the first time in nadir view, including nitrous acid, furan, acetylene, propylene, acetic acid, formaldehyde and hydrogen cyanide, observations which were made in a pyrocumulus cloud from the Australian bush fires of February 2009. Being able to observe this large number of reactive trace gases will likely improve our knowledge of source emissions and their impact on the environment and climate.

  2. In vitro toxicity of carbon nanotubes, nano-graphite and carbon black, similar impacts of acid functionalization.

    PubMed

    Figarol, Agathe; Pourchez, Jrmie; Boudard, Delphine; Forest, Valrie; Akono, Cline; Tulliani, Jean-Marc; Lecompte, Jean-Pierre; Cottier, Michle; Bernache-Assollant, Didier; Grosseau, Philippe

    2015-12-25

    Carbon nanotubes (CNT) and nano-graphite (NG) are graphene-based nanomaterials which share exceptional physicochemical properties, but whose health impacts are unfortunately still not well understood. On the other hand, carbon black (CB) is a conventional and widely studied material. The comparison of these three carbon-based nanomaterials is thus of great interest to improve our understanding of their toxicity. An acid functionalization was carried out on CNT, NG and CB so that, after a thorough characterization, their impacts on RAW 264.7 macrophages could be compared for a similar surface chemistry (15 to 120?gmL(-1) nanomaterials, 90-min to 24-h contact). Functionalized nanomaterials triggered a weak cytotoxicity similar to the pristine nanomaterials. Acid functionalization increased the pro-inflammatory response except for CB which did not trigger any TNF-? production before or after functionalization, and seemed to strongly decrease the oxidative stress. The toxicological impact of acid functionalization appeared thus to follow a similar trend whatever the carbon-based nanomaterial. At equivalent dose expressed in surface and equivalent surface chemistry, the toxicological responses from murine macrophages to NG were higher than for CNT and CB. It seemed to correspond to the hypothesis of a platelet and fiber paradigm. PMID:26381085

  3. Understanding in vivo carbon precursor supply for fatty acid synthesis in leaf tissue.

    PubMed

    Bao, X; Focke, M; Pollard, M; Ohlrogge, J

    2000-04-01

    The principal supply of carbon precursors for fatty acid synthesis in leaf tissue has been a much debated topic, with some experiments suggesting a direct supply from the C3 products of photosynthetic carbon fixation and colleagues suggesting the utilization of free acetate (for which concentrations in leaves in the range of 0.05-1.4 mM have been reported). To address this issue we first reassessed the in vivo rate of fatty acid synthesis using a new method, that of [13C]carbon dioxide labeling of intact Arabidopsis plants with the subsequent analysis of fatty acids by gas chromatography-mass spectrometry (GC-MS). This method gave an average value of 2.3 mmoles carbon atoms h-1 mg chlorophyll-1 for photosynthetic tissues. The method was extended by isotopic dilution analysis to measure the rate of fatty acid synthesis in the dark. There was negligible fatty acid synthesis (< 5% of the rate in the light) in the dark. In addition, the method allowed an estimate of the absolute rate of fatty acid degradation of about 4% of the total fatty acid content per day. With the in vivo rate of fatty acid synthesis in the light defined, if the bulk tissue acetate concentration available for fatty acid synthesis is 1 mM, this acetate pool can sustain fatty acid synthesis for approximately 60 min. When the leaves of Arabidopsis, barley and pea were given a 5 min pulse of [14C]carbon dioxide, the label rapidly appeared in fatty acids with a lag phase of less than 2-3 min. Continuous labeling with [14C]carbon dioxide, for up to 1 h, showed a similar result. Furthermore, 14C-label in free acetate was less than 5% of that in fatty acids. In conclusion, these data suggest that either the bulk pool of acetate is not involved in fatty acid synthesis or the concentration of acetate must be less than 0.05 mM under strong illumination. PMID:10792819

  4. Chemical and biological consequences of using carbon dioxide versus acid additions in ocean acidification experiments

    USGS Publications Warehouse

    Yates, Kimberly K.; DuFore, Christopher M.; Robbins, Lisa L.

    2013-01-01

    Use of different approaches for manipulating seawater chemistry during ocean acidification experiments has confounded comparison of results from various experimental studies. Some of these discrepancies have been attributed to whether addition of acid (such as hydrochloric acid, HCl) or carbon dioxide (CO2) gas has been used to adjust carbonate system parameters. Experimental simulations of carbonate system parameter scenarios for the years 1766, 2007, and 2100 were performed using the carbonate speciation program CO2SYS to demonstrate the variation in seawater chemistry that can result from use of these approaches. Results showed that carbonate system parameters were 3 percent and 8 percent lower than target values in closed-system acid additions, and 1 percent and 5 percent higher in closed-system CO2 additions for the 2007 and 2100 simulations, respectively. Open-system simulations showed that carbonate system parameters can deviate by up to 52 percent to 70 percent from target values in both acid addition and CO2 addition experiments. Results from simulations for the year 2100 were applied to empirically derived equations that relate biogenic calcification to carbonate system parameters for calcifying marine organisms including coccolithophores, corals, and foraminifera. Calculated calcification rates for coccolithophores, corals, and foraminifera differed from rates at target conditions by 0.5 percent to 2.5 percent in closed-system CO2 gas additions, from 0.8 percent to 15 percent in the closed-system acid additions, from 4.8 percent to 94 percent in open-system acid additions, and from 7 percent to 142 percent in open-system CO2 additions.

  5. Sources of black carbon aerosols in South Asia and surrounding regions during the Integrated Campaign for Aerosols, Gases and Radiation Budget (ICARB)

    SciTech Connect

    Kumar, R.; Barth, M. C.; Nair, V. S.; Pfister, G. G.; Suresh Babu, S.; Satheesh, S. K.; Moorthy, K. Krishna; Carmichael, G. R.; Lu, Z.; Streets, D. G.

    2015-05-19

    This study examines differences in the surface black carbon (BC) aerosol loading between the Bay of Bengal (BoB) and the Arabian Sea (AS) and identifies dominant sources of BC in South Asia and surrounding regions during March–May 2006 (Integrated Campaign for Aerosols, Gases and Radiation Budget, ICARB) period. A total of 13 BC tracers are introduced in the Weather Research and Forecasting Model coupled with Chemistry to address these objectives. The model reproduced the temporal and spatial variability of BC distribution observed over the AS and the BoB during the ICARB ship cruise and captured spatial variability at the inland sites. In general, the model underestimates the observed BC mass concentrations. However, the model–observation discrepancy in this study is smaller compared to previous studies. Model results show that ICARB measurements were fairly well representative of the AS and the BoB during the pre-monsoon season. Elevated BC mass concentrations in the BoB are due to 5 times stronger influence of anthropogenic emissions on the BoB compared to the AS. Biomass burning in Burma also affects the BoB much more strongly than the AS. Results show that anthropogenic and biomass burning emissions, respectively, accounted for 60 and 37% of the average ± standard deviation (representing spatial and temporal variability) BC mass concentration (1341 ± 2353 ng m-3) in South Asia. BC emissions from residential (61%) and industrial (23%) sectors are the major anthropogenic sources, except in the Himalayas where vehicular emissions dominate. We find that regional-scale transport of anthropogenic emissions contributes up to 25% of BC mass concentrations in western and eastern India, suggesting that surface BC mass concentrations cannot be linked directly to the local emissions in different regions of South Asia.

  6. Sources of black carbon aerosols in South Asia and surrounding regions during the Integrated Campaign for Aerosols, Gases and Radiation Budget (ICARB)

    SciTech Connect

    Kumar, R.; Barth, M. C.; Nair, V. S.; Pfister, G. G.; Babu, S. Suresh; Satheesh, S. K.; Moorthy, K. Krishna; Carmichael, G. R.; Lu, Z.; Streets, D. G.

    2015-01-01

    This study examines differences in the surface black carbon (BC) aerosol loading between the Bay of Bengal (BoB) and the Arabian Sea (AS) and identifies dominant sources of BC in South Asia and surrounding regions during March-May 2006 (Integrated Campaign for Aerosols, Gases and Radiation Budget, ICARB) period. A total of 13 BC tracers are introduced in the Weather Research and Forecasting Model coupled with Chemistry to address these objectives. The model reproduced the temporal and spatial variability of BC distribution observed over the AS and the BoB during the ICARB ship cruise and captured spatial variability at the inland sites. In general, the model underestimates the observed BC mass concentrations. However, the model-observation discrepancy in this study is smaller compared to previous studies. Model results show that ICARB measurements were fairly well representative of the AS and the BoB during the pre-monsoon season. Elevated BC mass concentrations in the BoB are due to 5 times stronger influence of anthropogenic emissions on the BoB compared to the AS. Biomass burning in Burma also affects the BoB much more strongly than the AS. Results show that anthropogenic and biomass burning emissions, respectively, accounted for 60 and 37% of the average +/- standard deviation (representing spatial and temporal variability) BC mass concentration (1341 +/- 2353 ng m(-3)) in South Asia. BC emissions from residential (61 %) and industrial (23 %) sectors are the major anthropogenic sources, except in the Himalayas where vehicular emissions dominate. We find that regional-scale transport of anthropogenic emissions contributes up to 25% of BC mass concentrations in western and eastern India, suggesting that surface BC mass concentrations cannot be linked directly to the local emissions in different regions of South Asia.

  7. Sources of black carbon aerosols in South Asia and surrounding regions during the Integrated Campaign for Aerosols, Gases and Radiation Budget (ICARB)

    DOE PAGESBeta

    Kumar, R.; Barth, M. C.; Nair, V. S.; Pfister, G. G.; Suresh Babu, S.; Satheesh, S. K.; Moorthy, K. Krishna; Carmichael, G. R.; Lu, Z.; Streets, D. G.

    2015-05-19

    This study examines differences in the surface black carbon (BC) aerosol loading between the Bay of Bengal (BoB) and the Arabian Sea (AS) and identifies dominant sources of BC in South Asia and surrounding regions during March–May 2006 (Integrated Campaign for Aerosols, Gases and Radiation Budget, ICARB) period. A total of 13 BC tracers are introduced in the Weather Research and Forecasting Model coupled with Chemistry to address these objectives. The model reproduced the temporal and spatial variability of BC distribution observed over the AS and the BoB during the ICARB ship cruise and captured spatial variability at the inlandmore » sites. In general, the model underestimates the observed BC mass concentrations. However, the model–observation discrepancy in this study is smaller compared to previous studies. Model results show that ICARB measurements were fairly well representative of the AS and the BoB during the pre-monsoon season. Elevated BC mass concentrations in the BoB are due to 5 times stronger influence of anthropogenic emissions on the BoB compared to the AS. Biomass burning in Burma also affects the BoB much more strongly than the AS. Results show that anthropogenic and biomass burning emissions, respectively, accounted for 60 and 37% of the average ± standard deviation (representing spatial and temporal variability) BC mass concentration (1341 ± 2353 ng m-3) in South Asia. BC emissions from residential (61%) and industrial (23%) sectors are the major anthropogenic sources, except in the Himalayas where vehicular emissions dominate. We find that regional-scale transport of anthropogenic emissions contributes up to 25% of BC mass concentrations in western and eastern India, suggesting that surface BC mass concentrations cannot be linked directly to the local emissions in different regions of South Asia.« less

  8. Sources of black carbon aerosols in South Asia and surrounding regions during the Integrated Campaign for Aerosols, Gases and Radiation Budget (ICARB)

    NASA Astrophysics Data System (ADS)

    Kumar, R.; Barth, M. C.; Nair, V. S.; Pfister, G. G.; Babu, S. S.; Satheesh, S. K.; Moorthy, K. K.; Carmichael, G. R.

    2014-12-01

    The dominant sources of black carbon (BC) in South Asia and surrounding regions are inferred during March-May 2006 (Integrated Campaign for Aerosols, Gases and Radiation Budget, ICARB) period by introducing BC tracers in the Weather Research and Forecasting Model coupled with Chemistry. The model reproduced the magnitude, temporal and spatial variability of BC distribution observed during the ICARB ship-cruise. Average and SD (representing the spatial and temporal variability) in observed and modeled BC mass concentrations along the ship-track are estimated as 755 ± 734 and 732 ± 913 ng m-3 respectively. Average modeled values at most of the inland stations were also found to fall within the range of observed values. Model results show that ICARB measurements were fairly well representative of the Arabian Sea and the Bay of Bengal during the pre-monsoon season. Results show that anthropogenic and biomass burning emissions, respectively, accounted for 70 and 28 % of the average ± SD BC mass concentration (1480 ± 5920 ng m-3) in South Asia. BC emissions from residential (49 %) and industrial (37 %) sectors appear to be the major anthropogenic sources, except in the Himalayas where vehicular emissions dominated. We find that, while all parts of continental India contributed to anthropogenic BC over the Bay of Bengal, contribution over the Arabian Sea came mostly from southern Peninsula. We also show that regional-scale transport of anthropogenic emissions contribute up to 30 % of BC mass concentrations in western and eastern India, suggesting that it is important to consider non-local sources along with the local emissions while designing strategies for mitigating BC emissions.

  9. Sources of Black Carbon Aerosols in South Asia and Surrounding Regions During the Integrated Campaign for Aerosols, Gases and Radiation Budget (ICARB)

    NASA Astrophysics Data System (ADS)

    Kumar, R.; Barth, M. C.; Nair, V. S.; Pfister, G.; Babu, S. S.; Satheesh, S. K.; Krishnamoorthy, K.; Carmichael, G. R.

    2014-12-01

    The dominant sources of black carbon (BC) in South Asia and surrounding regions are inferred during March-May 2006 (Integrated Campaign for Aerosols, Gases and Radiation Budget (ICARB)) by introducing BC tracers in the Weather Research and Forecasting Model coupled with Chemistry. Model results show that ICARB measurements were fairly well representative of the Arabian Sea and the Bay of Bengal during the pre-monsoon season. The model reproduced well the magnitude, temporal and spatial variability of BC concentrations observed during the ICARB ship-cruise. Average and standard deviation (representing the spatial and temporal variability) in observed and modeled BC mass concentrations along the ship-track are estimated as 755±734 ng m-3 and 732±913 ng m-3 respectively, where the standard deviation represents the spatial and temporal variability in the region. Average modeled values at most of the inland stations were also found to fall within the range of observed values. Results show that anthropogenic and biomass burning emissions, respectively, accounted for 70% and 28% of the BC mass concentration in South Asia. BC emissions from residential (49%) and industrial (37%) sectors appear to be the major anthropogenic sources, except in the Himalayas where vehicular emissions dominate. We find that, while all parts of continental India contributed to anthropogenic BC over Bay of Bengal, contribution over the Arabian Sea came mostly from southern Peninsula. We also show that long-range transport of anthropogenic emissions contribute up to 30% of BC concentrations in western and eastern India, suggesting that it is important to consider non-local sources along with the local emissions while designing strategies for mitigating BC emissions.

  10. Influence of acid functionalization on the cardiopulmonary toxicity of carbon nanotubes and carbon black particles in mice

    SciTech Connect

    Tong Haiyan McGee, John K.; Saxena, Rajiv K.; Kodavanti, Urmila P.; Devlin, Robert B.; Gilmour, M. Ian

    2009-09-15

    Engineered carbon nanotubes are being developed for a wide range of industrial and medical applications. Because of their unique properties, nanotubes can impose potentially toxic effects, particularly if they have been modified to express functionally reactive chemical groups on their surface. The present study was designed to evaluate whether acid functionalization (AF) enhanced the cardiopulmonary toxicity of single-walled carbon nanotubes (SWCNT) as well as control carbon black particles. Mice were exposed by oropharyngeal aspiration to 10 or 40 {mu}g of saline-suspended single-walled carbon nanotubes (SWCNTs), acid-functionalized SWCNTs (AF-SWCNTs), ultrafine carbon black (UFCB), AF-UFCB, or 2 {mu}g LPS. 24 hours later, pulmonary inflammatory responses and cardiac effects were assessed by bronchoalveolar lavage and isolated cardiac perfusion respectively, and compared to saline or LPS-instilled animals. Additional mice were assessed for histological changes in lung and heart. Instillation of 40 {mu}g of AF-SWCNTs, UFCB and AF-UFCB increased percentage of pulmonary neutrophils. No significant effects were observed at the lower particle concentration. Sporadic clumps of particles from each treatment group were observed in the small airways and interstitial areas of the lungs according to particle dose. Patches of cellular infiltration and edema in both the small airways and in the interstitium were also observed in the high dose group. Isolated perfused hearts from mice exposed to 40 {mu}g of AF-SWCNTs had significantly lower cardiac functional recovery, greater infarct size, and higher coronary flow rate than other particle-exposed animals and controls, and also exhibited signs of focal cardiac myofiber degeneration. No particles were detected in heart tissue under light microscopy. This study indicates that while acid functionalization increases the pulmonary toxicity of both UFCB and SWCNTs, this treatment caused cardiac effects only with the AF-carbon nanotubes. Further experiments are needed to understand the physico-chemical processes involved in this phenomenon.

  11. Toxicity of pyrolysis gases from polyoxymethylene

    NASA Technical Reports Server (NTRS)

    Hilado, C. J.; Schneider, J. E.; Brauer, D. P.

    1979-01-01

    A sample of polyoxymethylene was evaluated for toxicity of pyrolysis gases, using the toxicity screening test method developed at the University of San Francisco. Under several test conditions, this material gave shorter times to death than many other synthetic polymers. Carbon monoxide appeared to be the principal toxicant in the pyrolysis gases.

  12. 40 CFR 86.1514 - Analytical gases.

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ... carbon monoxide on a dry basis. (b) If the raw CO sampling system specified in 40 CFR part 1065 is used, the analytical gases specified in 40 CFR part 1065, subpart H, shall be used. (c) If a CVS sampling system is used, the analytical gases specified in 40 CFR part 1065, subpart H, shall be used....

  13. 40 CFR 86.1514 - Analytical gases.

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... carbon monoxide on a dry basis. (b) If the raw CO sampling system specified in 40 CFR part 1065 is used, the analytical gases specified in 40 CFR part 1065, subpart H, shall be used. (c) If a CVS sampling system is used, the analytical gases specified in 40 CFR part 1065, subpart H, shall be used....

  14. Carbon dioxide-sustained adsorption of lactic acid at pH > pK{sub a} of the acid

    SciTech Connect

    Husson, S.M.; King, C.J.

    1999-04-01

    Experimental data are presented for batch and fixed-bed adsorption of lactic acid from aqueous sodium lactate solutions onto the tertiary amine sorbents, Dowex MWA-1 and Amberlite IRA-35, in the presence of carbon dioxide. The effects of carbon dioxide pressure and sodium lactate concentration on lactate uptake capacity were measured. A simple complexation model, which includes chemical-equilibria and mass- and charge-balance equations, was developed to describe the system. There are no fitted parameters in the model. The model predictions compare well with batch adsorption data.

  15. The Path of Carbon in Photosynthesis VIII. The Role of Malic Acid

    DOE R&D Accomplishments Database

    Bassham, James A.; Benson, Andrew A.; Calvin, Melvin

    1950-01-25

    Malonate has been found to inhibit the formation of malic acid during short periods of photosynthesis with radioactive carbon dioxide. This result, together with studies which show the photosynthetic cycle to be operating normally at the same time, indicates that malic acid is not an intermediate in photosynthesis but is probably closely related to some intermediate of the cycle. Absence of labeled succinic and fumaric acids in these experiments, in addition to the failure of malonate to inhibit photosynthesis, precludes the participation of these acids as intermediates in photosynthesis.

  16. Synthesis of sulfonated porous carbon nanospheres solid acid by a facile chemical activation route

    SciTech Connect

    Chang, Binbin Guo, Yanzhen; Yin, Hang; Zhang, Shouren; Yang, Baocheng

    2015-01-15

    Generally, porous carbon nanospheres materials are usually prepared via a template method, which is a multi-steps and high-cost strategy. Here, we reported a porous carbon nanosphere solid acid with high surface area and superior porosity, as well as uniform nanospheical morphology, which prepared by a facile chemical activation with ZnCl{sub 2} using resorcinol-formaldehyde (RF) resins spheres as precursor. The activation of RF resins spheres by ZnCl{sub 2} at 400 °C brought high surface area and large volume, and simultaneously retained numerous oxygen-containing and hydrogen-containing groups due to the relatively low processing temperature. The presence of these functional groups is favorable for the modification of –SO{sub 3}H groups by a followed sulfonation treating with sulphuric acid and organic sulfonic acid. The results of N{sub 2} adsorption–desorption and electron microscopy clearly showed the preservation of porous structure and nanospherical morphology. Infrared spectra certified the variation of surface functional groups after activation and the successful modification of –SO{sub 3}H groups after sulfonation. The acidities of catalysts were estimated by an indirect titration method and the modified amount of –SO{sub 3}H groups were examined by energy dispersive spectra. The results suggested sulfonated porous carbon nanospheres catalysts possessed high acidities and –SO{sub 3}H densities, which endowed their significantly catalytic activities for biodiesel production. Furthermore, their excellent stability and recycling property were also demonstrated by five consecutive cycles. - Graphical abstract: Sulfonated porous carbon nanospheres with high surface area and superior catalytic performance were prepared by a facile chemical activation route. - Highlights: • Porous carbon spheres solid acid prepared by a facile chemical activation. • It owns high surface area, superior porosity and uniform spherical morphology. • It possesses high acidity and high –SO{sub 3}H density. • It exhibits excellently catalytic performance for esterification of oleic acid.

  17. Preliminary simulations of planned experiments to study the impact of trace gases on the capacity of the Weyburn-Midale field to store carbon dioxide

    SciTech Connect

    Carroll, S; Hao, Y

    2009-11-13

    The CO{sub 2} stream injecting into the Weyburn-Midale field can be generally classified as a reducing stream with residual H{sub 2}S and low-molecular weight hydrocarbons. The composition of the CO{sub 2} gas stream from the Dakota Gasification Company is reported to be 95% CO{sub 2}, 4% hydrocarbons, and 1% H{sub 2}S by volume (Huxley 2006). In addition to the H{sub 2}S introduced at the injection wells, significant concentrations of H{sub 2}S are thought to have been produced in-situ by sulfate reducing bacteria from previous water floods for enhanced oil production. Produced gas compositions range in H{sub 2}S concentrations from 1 to 6 volume percent. The produced gas, including the trace impurities, is re-injected into the field. Although there is no evidence for inorganic reduction of SO{sub 4}{sup 2-} to H{sub 2}S at the Weyburn-Midale field, Sitchler and Kazuba (2009) suggest that SO{sub 4}{sup 2-} can be inorganically reduced to elemental sulfur in highly reducing environments based on a natural analog study of the Madison Formation in Wyoming. They propose that elevated concentrations of CO{sub 2} dissolve anhydrite to produce the sulfate that is then reduced. Oxidizing CO{sub 2} streams with residual O{sub 2} and SO{sub 2} typical of streams captured from oxyfuel and post combustion processes are not presently an issue at the Weyburn-Midale field. However it is possible that the oxidizing CO{sub 2} streams may be injected in the future in carbonate reservoirs similar to the Weyburn-Midale field. To date there are few modeling and experimental studies that have explored the impact of impurity gases in CO{sub 2} streams targeted for geologic storage (Gale 2009). Jacquemet et al (2009) reviewed select geochemical modeling studies that explored the impact of SO{sub 2} and H{sub 2}S impurities in the waste streams (Gunter et al., 2000, Knauss et al., 2005, Xu et al., 2007). These studies collectively show that SO{sub 2} significantly reduces the pH when oxidized to H{sub 2}SO{sub 4} causing enhanced dissolution of carbonate minerals and some sulfate mineral precipitation. Low pH results in higher mineral solubility and faster dissolution rates and is thought to enhance porosity and permeability near the injection well when trace amounts of SO{sub 2} is injected with CO{sub 2}. The impact of H{sub 2}S on storage reservoir performance appears to more subtle. Knauss et al (2005) report no significant impacts of injection of CO{sub 2} gas streams with and without H{sub 2}S (1 M Pascal H{sub 2}S + 8.4 M Pascal CO{sub 2}) in simulations of CO{sub 2} storage in the Frio sandstone formation. Geochemical reactions for H{sub 2}S impurities include enhance field alkalinity and reaction with iron bearing minerals that may delay breakthrough of H{sub 2}S relative to CO{sub 2}. Emberley et al. (2005) report that half of the alkalinity measured at monitoring wells at the Weyburn-Midale field is due to HS{sup -}. Schoonen and Xu (2004) report that H{sub 2}S can be sequestered as pyrite in sandstones and carbonates by dissolving iron hydroxides and iron-bearing clays. Similarly, Gunter et al (2000) propose the that siderite converts to iron sulfides when it is reacted with H{sub 2}S. The geochemical reactions between H{sub 2}S and iron bearing minerals together with the high solubility of H{sub 2}S relative to CO{sub 2} may contribute to the delayed break though of H{sub 2}S in experiments. A few core flood experiments have shown that the injection of supercritical CO{sub 2} into carbonate aquifers has the potential to significantly alter the porosity in the absence of trace gases such as SO{sub 2} and H{sub 2}S. Luquot and Gouze (2009) documented a 2% porosity increase in carbonate cores when rock-water interactions were transport limited and solution concentrations were closer to equilibrium and a 4% porosity increase when rock-water interactions were reaction limited and solution compositions were further from equilibrium. Similarly Le Guen et al (2007) used x-ray micro-tomography and geochemistry to show that porosity signific

  18. Postillumination burst of carbon dioxide in crassalacean Acid metabolism plants.

    PubMed

    Crews, C E; Vines, H M; Black, C C

    1975-04-01

    Immediately following exposure to light, a postillumination burst of CO(2) has been detected in Crassulacean acid metabolism plants. A detailed study with pineapple (Ananas comosus) leaves indicates that the postillumination burst changes its amplitude and kinetics during the course of a day. In air, the postillumination burst in pineapple leaves generally is exhibited as two peaks. The postillumination burst is sensitive to atmospheric CO(2) and O(2) concentrations as well as to the light intensity under which plants are grown. We propose that the CO(2) released in the first postillumination burst peak is indicative of photorespiration since it is sensitive to either O(2) or CO(2) concentration while the second CO(2) evolution peak is likely due to decarboxylation of organic acids involved in Crassulacean acid metabolism.In marked contrast to other higher plants, the postillumination burst in Crassulacean acid metabolism plants can be equal to or greater than the rate of photosynthesis. Photosynthesis in pineapple leaves also varies throughout a day. Both photosynthesis and the postillumination burst have a daily variation which apparently is a complex function of degree of leaf acidity, growth light intensity, ambient gas phase, and the time a plant has been exposed to a given gas. PMID:16659142

  19. Assessing the potential of amino acid δ13C patterns as a carbon source tracer in marine sediments: effects of algal growth conditions and sedimentary diagenesis

    NASA Astrophysics Data System (ADS)

    Larsen, T.; Bach, L. T.; Salvatteci, R.; Wang, Y. V.; Andersen, N.; Ventura, M.; McCarthy, M. D.

    2015-01-01

    Burial of organic carbon in marine sediments has a profound influence in marine biogeochemical cycles, and provides a sink for greenhouse gases such as CO2 and CH4. However, tracing organic carbon from primary production sources as well as its transformations in the sediment record remains challenging. Here we examine a novel but growing tool for tracing biosynthetic origin of amino acid carbon skeletons, based on natural occurring stable carbon isotope patterns in individual amino acids (δ13CAA). We focus on two important aspects for δ13CAA utility in sedimentary paleoarchives: first, the fidelity of source diagnostic of algal δ13CAA patterns across different oceanographic growth conditions; and second, the ability of δ13CAA patterns to record the degree of subsequent microbial amino acid synthesis after sedimentary burial. Using the marine diatom Thalassiosira weissflogii, we tested under controlled conditions how δ13CAA patterns respond to changing environmental conditions, including light, salinity, temperature, and pH. Our findings show that while differing oceanic growth conditions can change macromolecular cellular composition, δ13CAA isotopic patterns remain largely invariant. These results underscore that δ13CAA patterns should accurately record biosynthetic sources across widely disparate oceanographic conditions. We also explored how δ13CAA patterns change as a function of age, total nitrogen and organic carbon content after burial, in a marine sediment core from a coastal upwelling area off Peru. Based on the four most informative amino acids for distinguishing between diatom and bacterial sources (i.e. isoleucine, lysine, leucine and tyrosine), bacterial derived amino acids ranged from 10-15% in the sediment layers from the last 5000 years to 35% during the last glacial period. The larger bacterial fractions in older sediments indicate that bacterial activity and amino acid resynthesis progressed, approximately as a function of sediment age, to a substantially larger degree than suggested by changes in total organic nitrogen and carbon content. Taken together, these culturing and sediment studies suggest that δ13CAA patterns in sediments represent a novel proxy for understanding both primary production sources, as well as direct bacterial role in the ultimate preservation of sedimentary organic matter.

  20. Monodispersed Hollow SO3H-Functionalized Carbon/Silica as Efficient Solid Acid Catalyst for Esterification of Oleic Acid.

    PubMed

    Wang, Yang; Wang, Ding; Tan, Minghui; Jiang, Bo; Zheng, Jingtang; Tsubaki, Noritatsu; Wu, Mingbo

    2015-12-01

    SO3H-functionalized monodispersed hollow carbon/silica spheres (HS/C-SO3H) with primary mesopores were prepared with polystyrene as a template and p-toluenesulfonic acid (TsOH) as a carbon precursor and -SO3H source simultaneously. The physical and chemical properties of HS/C-SO3H were characterized by N2 adsorption, TEM, SEM, XPS, XRD, Raman spectrum, NH3-TPD, element analysis and acid-base titration techniques. As a solid acid catalyst, HS/C-SO3H shows excellent performance in the esterification of oleic acid with methanol, which is a crucial reaction in biodiesel production. The well-defined hollow architecture and enhanced active sites accessibility of HS/C-SO3H guarantee the highest catalytic performance compared with the catalysts prepared by activation of TsOH deposited on the ordered mesoporous silicas SBA-15 and MCM-41. At the optimized conditions, high conversion (96.9%) was achieved and no distinct activity drop was observed after 5 recycles. This synthesis strategy will provide a highly effective solid acid catalyst for green chemical processes. PMID:26588826

  1. Carbon isotope composition of low molecular weight hydrocarbons and monocarboxylic acids from Murchison meteorite

    NASA Technical Reports Server (NTRS)

    Yuen, G.; Blair, N.; Des Marais, D. J.; Chang, S.

    1984-01-01

    Carbon isotopic compositions have been measured for individual hydrocarbons and monocarboxylic acids from the Murchison meteorite, a C2 carbonaceous chondrite which fell in Australia in 1969. With few exceptions, notably benzene, the volatile products are substantially isotopically heavier than their terrestrial counterparts, signifying their extraterrestrial origin. For both classes of compounds, the ratio of C-13 to C-12 decreases with increasing carbon number in a roughly parallel manner, and each carboxylic acid exhibits a higher isotopic ratio than the hydrocarbon containing the same number of carbon atoms. These trends are consistent with the kinetically controlled synthesis of higher homologues from lower ones. The results suggest the possibility that the production mechanisms for hydrocarbons and carboxylic acids may be similar, and impose constraints on the identity of the reactant species.

  2. One-Pot synthesis of phosphorylated mesoporous carbon heterogeneous catalysts with tailored surface acidity

    SciTech Connect

    Fulvio, Pasquale F; Mahurin, Shannon Mark; Mayes, Richard T; Bauer, Christopher; Wang, Xiqing; Veith, Gabriel M; Dai, Sheng

    2012-01-01

    Soft-templated phosphorylated mesoporous carbons with homogeneous distributions of phosphate groups were prepared by a 'one-pot' synthesis method using mixtures of phosphoric acid with hydrochloric, or nitric acids in the presence of Pluronic F127 triblock copolymer. Adjusting the various ratios of phosphoric acid used in these mixtures resulted in carbons with distinct adsorption, structural and surface acidity properties. The pore size distributions (PSDs) from nitrogen adsorption at -196 C showed that mesoporous carbons exhibit specific surface areas as high as 551 m{sup 2}/g and mesopores as large as 13 nm. Both structural ordering of the mesopores and the final phosphate contents were strongly dependent on the ratios of H{sub 3}PO{sub 4} in the synthesis gels, as shown by transmission electron microscopy (TEM), X-ray photoelectron (XPS) and energy dispersive X-ray spectroscopy (EDS). The number of surface acid sites determined from temperature programmed desorption of ammonia (NH{sub 3}-TPD) were in the range of 0.3-1.5 mmol/g while the active surface areas are estimated to comprise 5-54% of the total surface areas. Finally, the conversion temperatures for the isopropanol dehydration were lowered by as much as 100 C by transitioning from the least acidic to the most acidic catalysts surface.

  3. Conversion of carbon dioxide to resorcylic acid under ultrasonication by Kolbe-Schmitt reaction.

    PubMed

    Shanthi, B; Palanivelu, K

    2015-11-01

    The present work focuses on a new approach for the synthesis of ?-resorcylic acid based on Kolbe-Schmitt reaction using carbon dioxide under ultrasonic and mild condition. The Kolbe-Schmitt reaction is a process for the synthesis of ?-resorcylic acid (2,4-dihydroxybenzoic acid) from resorcinol in aqueous potassium hydroxide solution with gaseous CO2. The influences of carbonation time, flow rate of CO2 and the molar ratio of resorcinol/potassium hydroxide on the yield percentage of resorcylic acid were investigated. The study was assessed with the conventional thermal method (non ultrasonic method) for Kolbe-Schmitt reaction and it was observed that applying ultrasound to save more than 95% and 38.6% energy as shown by energy consumption calculations in bath type and horn type sonicator respectively. ?-Resorcylic acid formed was characterized by (1)H NMR, (13)C NMR, DEPT NMR and FTIR spectroscopy. The amount of CO2 utilized in the reaction was evaluated from the yield percentage of ?-resorcylic acid yield. The maximum yield of resorcylic acid of 30% and 65% was obtained at the resorcinol/potassium hydroxide ratio of 1:3, carbonation time of 150 min and the CO2 flow rate of 2L/min in bath type and horn type ultrasonicator, respectively. The applicability of the research work was examined in two different positional isomers of resorcinol under optimum conditions. PMID:26186845

  4. Capture and release of acid-gasses with acid-gas binding organic compounds

    DOEpatents

    Heldebrant, David J; Yonker, Clement R; Koech, Phillip K

    2015-03-17

    A system and method for acid-gas capture wherein organic acid-gas capture materials form hetero-atom analogs of alkyl-carbonate when contacted with an acid gas. These organic-acid gas capture materials include combinations of a weak acid and a base, or zwitterionic liquids. This invention allows for reversible acid-gas binding to these organic binding materials thus allowing for the capture and release of one or more acid gases. These acid-gas binding organic compounds can be regenerated to release the captured acid gasses and enable these organic acid-gas binding materials to be reused. This enables transport of the liquid capture compounds and the release of the acid gases from the organic liquid with significant energy savings compared to current aqueous systems.

  5. SORPTION OF MERCURY SPECIES BY ACTIVATED CARBONS AND CALCIUM-BASES SORBENTS: EFFECT OF TEMPERATURE, MERCURY CONCENTRATION AND ACID GASES

    EPA Science Inventory

    Bench-scale studies of mercury/sorbent reactions were conducted to understand mechanistic limitations of field-scale attempts to reduce emissions of mercury from combustion processes. The effects of temperature (60 - 140 degrees C), sulfur dioxide (SO2, 1000 ppm ), hydrogen chlor...

  6. Catalytic ozonation of p-chlorobenzoic acid by activated carbon and nickel supported activated carbon prepared from petroleum coke.

    PubMed

    Li, Xukai; Zhang, Qiuyun; Tang, Lili; Lu, Ping; Sun, Fengqiang; Li, Laisheng

    2009-04-15

    The aim of this research was to investigate catalytic activity of petroleum coke, activated carbon (AC) prepared from this material, Ni supported catalyst on activated carbon (Ni/AC) in the ozonation of aqueous phase p-chlorobenzoic acid (p-CBA). Activated carbon and Ni/AC catalyst were characterized by XRD and SEM. The presence of petroleum coke did not improve the degradation of p-CBA compared to ozonation alone, but it was advantageous for p-CBA mineralization (total organic carbon, TOC, reduction), indicating the generation of highly oxidant species (*OH) in the medium. The presence of either activated carbon or Ni/AC considerably improves TOC removal during p-CBA ozonation. Ni/AC catalyst shows the better catalytic activity and stability based on five repeated tests during p-CBA ozonation. During the ozonation (50 mg/h ozone flow rate) of a 10 mg/L p-CBA (pH 4.31), it can be more mineralized in the presence of Ni/AC catalyst (5.0 g/L), TOC removal rate is over 60% in 60 min, 43% using activated carbon as catalyst, only 30% with ozonation alone. PMID:18667273

  7. Carbonic acid as a reserve of carbon dioxide on icy moons: The formation of carbon dioxide (CO{sub 2}) in a polar environment

    SciTech Connect

    Jones, Brant M.; Kaiser, Ralf I.; Strazzulla, Giovanni

    2014-06-20

    Carbon dioxide (CO{sub 2}) has been detected on the surface of several icy moons of Jupiter and Saturn via observation of the ν{sub 3} band with the Near-Infrared Mapping Spectrometer on board the Galileo spacecraft and the Visible-Infrared Mapping Spectrometer on board the Cassini spacecraft. Interestingly, the CO{sub 2} band for several of these moons exhibits a blueshift along with a broader profile than that seen in laboratory studies and other astrophysical environments. As such, numerous attempts have been made in order to clarify this abnormal behavior; however, it currently lacks an acceptable physical or chemical explanation. We present a rather surprising result pertaining to the synthesis of carbon dioxide in a polar environment. Here, carbonic acid was synthesized in a water (H{sub 2}O)-carbon dioxide (CO{sub 2}) (1:5) ice mixture exposed to ionizing radiation in the form of 5 keV electrons. The irradiated ice mixture was then annealed, producing pure carbonic acid which was then subsequently irradiated, recycling water and carbon dioxide. However, the observed carbon dioxide ν{sub 3} band matches almost exactly with that observed on Callisto; subsequent temperature program desorption studies reveal that carbon dioxide synthesized under these conditions remains in solid form until 160 K, i.e., the sublimation temperature of water. Consequently, our results suggest that carbon dioxide on Callisto as well as other icy moons is indeed complexed with water rationalizing the shift in peak frequency, broad profile, and the solid state existence on these relatively warm moons.

  8. Heterogeneous reactions of gaseous hydrogen peroxide on pristine and acidic gas-processed calcium carbonate particles: Effects of relative humidity and surface coverage of coating

    NASA Astrophysics Data System (ADS)

    Zhao, Yue; Chen, Zhongming; Shen, Xiaoli; Huang, Dao

    2013-03-01

    Atmospheric aging appears to alter physical and chemical properties of mineral dust aerosol and thus its role as reactive surface in the troposphere. Yet, previous studies in the atmosphere have mainly focused on the pristine surfaces of mineral dust aerosol, and the reactivity of aged mineral dust toward atmospheric trace gases is poorly recognized. This work presents the first laboratory investigation of heterogeneous reactions of gaseous hydrogen peroxide (H2O2), an important atmospheric oxidant, on the surfaces of HNO3 and SO2-processed calcium carbonate particles as surrogates of atmospheric mineral dust aged by acidic trace gases. It is found that the processing of the calcium carbonate particles with HNO3 and SO2 has a strong impact on their reactivity toward H2O2. On HNO3-processed particles, the presence of nitrate acts to either decrease or increase H2O2 uptake, greatly depending on RH and surface coverage of nitrate. On SO2-processed particles, the presence of surface sulfite appears to enhance the intrinsic reactivity of the mineral particles due to its affinity for H2O2, and the uptake of H2O2 increases significantly relative to the pristine particles, in particular at high RH. The mechanisms for heterogeneous reactions of H2O2 with these processed particles are discussed, as well as their potential implications on tropospheric chemistry. The results of our study suggest that the reactivity of mineral dust aerosol toward H2O2 and maybe other trace gases is markedly dependent on the chemical composition and coverage of the coatings as well as ambient RH, and thus will vary considerably in different polluted air masses.

  9. Recovery of calcium carbonate from steelmaking slag and utilization for acid mine drainage pre-treatment.

    PubMed

    Mulopo, J; Mashego, M; Zvimba, J N

    2012-01-01

    The conversion of steelmaking slag (a waste product of the steelmaking process) to calcium carbonate (CaCO(3)) was tested using hydrochloric acid, ammonium hydroxide and carbon dioxide via a pH-swing process. Batch reactors were used to assess the technical feasibility of calcium carbonate recovery and its use for pre-treatment of acid mine drainage (AMD) from coal mines. The effects of key process parameters, such as the amount of acid (HCl/calcium molar ratio), the pH and the CO(2) flow rate were considered. It was observed that calcium extraction from steelmaking slag significantly increased with an increase in the amount of hydrochloric acid. The CO(2) flow rate also had a positive effect on the carbonation reaction rate but did not affect the morphology of the calcium carbonate produced for values less than 2 L/min. The CaCO(3) recovered from the bench scale batch reactor demonstrated effective neutralization ability during AMD pre-treatment compared with the commercial laboratory grade CaCO(3). PMID:22643421

  10. Multi-walled carbon nanotubes in aqueous phytic acid for enhancing biosensor

    NASA Astrophysics Data System (ADS)

    Guo, Xiaoyu; Miao, Yun; Ye, Pingping; Wen, Ying; Yang, Haifeng

    2014-04-01

    The poor dispersion of carbon based nanomaterials without strong acid pretreatment in aqueous solution is a fundamental problem, limiting its applications in biology-related fields. A good dispersion of multi-walled carbon nanotubes (MWCNTs) in water was realized by 50 wt.% phytic acid (PA) solution. As an application case, the PA-MWCNTs dispersion in aqueous solution was used for the immobilization of horseradish peroxidase (HRP) and its direct electrochemistry was realized. The constructed biosensor has a sound limit of detection, wide linear range, and high affinity for hydrogen peroxide (H2O2) as well as being free from interference of co-existing electro-active species.

  11. Acetaldehyde stimulation of net gluconeogenic carbon movement from applied malic acid in tomato fruit pericarp tissue

    SciTech Connect

    Halinska, A.; Frenkel, C. )

    1991-03-01

    Applied acetaldehyde is known to lead to sugar accumulation in fruit including tomatoes (Lycopersicon esculentum) presumably due to stimulation of gluconeogenesis. This conjecture was examined using tomato fruit pericarp discs as a test system and applied l-(U-{sup 14}C)malic acid as the source for gluconeogenic carbon mobilization. Results indicate that malic and perhaps other organic acids are carbon sources for gluconeogenesis occurring normally in ripening tomatoes. The process is stimulated by acetaldehyde apparently by attenuating the fructose-2,6-biphosphate levels. The mode of the acetaldehyde regulation of fructose-2,6-biphosphate metabolism awaits clarification.

  12. Carbon honeycomb grids for advanced lead-acid batteries. Part III: Technology scale-up

    NASA Astrophysics Data System (ADS)

    Kirchev, A.; Serra, L.; Dumenil, S.; Brichard, G.; Alias, M.; Jammet, B.; Vinit, L.

    2015-12-01

    The carbon honeycomb grid technology employs new carbon/carbon composites with ordered 3D structure instead of the classic lead-acid battery current collectors. The technology is laboratory scaled up from small size grids corresponding to electrodes with a capacity of 3 Ah to current collectors suitable for assembly of lead-acid batteries covering the majority of the typical lead-acid battery applications. Two series of 150 grids each (one positive and one negative) are manufactured using low-cost lab-scale equipment. They are further subjected to pasting with active materials and the resulting battery plates are assembled in 12 V AGM-VLRA battery mono-blocks for laboratory testing and outdoor demonstration in electric scooter replacing its original VRLAB pack. The obtained results demonstrate that the technology can replace successfully the state of the art negative grids with considerable benefits. The use of the carbon honeycomb grids as positive plate current collectors is limited by the anodic corrosion of the entire structure attacking both the carbon/carbon composite part and the electroplated lead-tin alloy coating.

  13. Removal of free fatty acid in Palm Fatty Acid Distillate using sulfonated carbon catalyst derived from biomass wastefor biodiesel production

    NASA Astrophysics Data System (ADS)

    Hidayat, Arif; Rochmadi; Wijaya, Karna; Budiman, Arief

    2016-01-01

    In this research, the esterification of PFAD using the sulfonatedcoconut shell biochar catalyst was studied. Carbon solid catalysts were prepared by a sulfonation of carbonized coconut shells. The performances of the catalysts were evaluated in terms of the reaction temperatures, the molar ratios of methanol to PFAD, the catalyst loading and the reaction times. The reusability of the solid acid carbon catalysts was also studied in this work. The results indicated that the FFA conversion was significantly increased with increasing catalyst loading and reaction times. It can be concluded that the optimal conditions were an PFAD to methanol molar ratio of 1:12, the amount of catalyst of 10%w, and reaction temperature of 60oC.At this optimum condition, the conversion to biodieselreached 88%.

  14. Corrosion effects of hydrogen sulfide on coiled tubing and carbon steel in hydrochloric acid

    SciTech Connect

    1997-09-01

    Coiled tubing is commonly used in oilwell drilling and stimulation. It has been reported to be less susceptible to acid attack than carbon steel in acidizing. Corrosion problems are frequently reported from field activities and include corrosion/erosion, galvanic attack, brine/oxygen/acid attack, and HCl/H{sub 2}S attack. In this study, coiled tubing was exposed to inhibited HCl acid in the presence and absence of H{sub 2}S. Four HCl inhibitors and one H{sub 2}S inhibitor were evaluated, and the corrosion rates of coiled tubing, carbon steel (J-55), and carburized steel were compared. Tests were conducted at atmospheric pressure for temperatures less than and equal to 200 F. At temperatures greater than 200 F; tests were conducted at 4,000 psi.

  15. Rhizosphere bacterial carbon turnover is higher in nucleic acids than membrane lipids: implications for understanding soil carbon cycling

    PubMed Central

    Malik, Ashish A.; Dannert, Helena; Griffiths, Robert I.; Thomson, Bruce C.; Gleixner, Gerd

    2015-01-01

    Using a pulse chase 13CO2 plant labeling experiment we compared the flow of plant carbon into macromolecular fractions of rhizosphere soil microorganisms. Time dependent 13C dilution patterns in microbial cellular fractions were used to calculate their turnover time. The turnover times of microbial biomolecules were found to vary: microbial RNA (19 h) and DNA (30 h) turned over fastest followed by chloroform fumigation extraction-derived soluble cell lysis products (14 days), while phospholipid fatty acids (PLFAs) had the slowest turnover (42 days). PLFA/NLFA 13C analyses suggest that both mutualistic arbuscular mycorrhizal and saprophytic fungi are dominant in initial plant carbon uptake. In contrast, high initial 13C enrichment in RNA hints at bacterial importance in initial C uptake due to the dominance of bacterial derived RNA in total extracts of soil RNA. To explain this discrepancy, we observed low renewal rate of bacterial lipids, which may therefore bias lipid fatty acid based interpretations of the role of bacteria in soil microbial food webs. Based on our findings, we question current assumptions regarding plant-microbe carbon flux and suggest that the rhizosphere bacterial contribution to plant assimilate uptake could be higher. This highlights the need for more detailed quantitative investigations with nucleic acid biomarkers to further validate these findings. PMID:25914679

  16. Rhizosphere bacterial carbon turnover is higher in nucleic acids than membrane lipids: implications for understanding soil carbon cycling.

    PubMed

    Malik, Ashish A; Dannert, Helena; Griffiths, Robert I; Thomson, Bruce C; Gleixner, Gerd

    2015-01-01

    Using a pulse chase (13)CO2 plant labeling experiment we compared the flow of plant carbon into macromolecular fractions of rhizosphere soil microorganisms. Time dependent (13)C dilution patterns in microbial cellular fractions were used to calculate their turnover time. The turnover times of microbial biomolecules were found to vary: microbial RNA (19 h) and DNA (30 h) turned over fastest followed by chloroform fumigation extraction-derived soluble cell lysis products (14 days), while phospholipid fatty acids (PLFAs) had the slowest turnover (42 days). PLFA/NLFA (13)C analyses suggest that both mutualistic arbuscular mycorrhizal and saprophytic fungi are dominant in initial plant carbon uptake. In contrast, high initial (13)C enrichment in RNA hints at bacterial importance in initial C uptake due to the dominance of bacterial derived RNA in total extracts of soil RNA. To explain this discrepancy, we observed low renewal rate of bacterial lipids, which may therefore bias lipid fatty acid based interpretations of the role of bacteria in soil microbial food webs. Based on our findings, we question current assumptions regarding plant-microbe carbon flux and suggest that the rhizosphere bacterial contribution to plant assimilate uptake could be higher. This highlights the need for more detailed quantitative investigations with nucleic acid biomarkers to further validate these findings. PMID:25914679

  17. On the abiotic formation of amino acids. I - HCN as a precursor of amino acids detected in extracts of lunar samples. II - Formation of HCN and amino acids from simulated mixtures of gases released from lunar samples

    NASA Technical Reports Server (NTRS)

    Yuasa, S.; Flory, D.; Basile, B.; Oro, J.

    1984-01-01

    Two studies on the abiotic formation of amino acids are presented. The first study demonstrates the role of hydrogen cyanide as a precursor of amino acids detected in extracts of lunar samples. The formation of several amino acids, including glycine, alanine, aspartic acid, and glutamic acid, under conditions similar to those used for the analysis of lunar samples is demonstrated. The second study investigates the formation of hydrogen cyanide as well as amino acids from lunar-sample gas mixtures under electrical discharge conditions. These results extend the possibility of synthesis of amino acids to planetary bodies with primordial atmospheres less reducing than a mixture of methane, ammonia, hydrogen and water.

  18. Characterization of the origin of coalbed gases in southeastern Illinois Basin by compound-specific carbon and hydrogen stable isotope ratios

    USGS Publications Warehouse

    Strapoc, D.; Mastalerz, Maria; Eble, C.; Schimmelmann, A.

    2007-01-01

    Coalbed gases and waters from exploratory and production gas wells in the southeastern Illinois Basin were sampled to assess geochemically the origin of coalbed gases, with an emphasis on the Springfield and Seelyville Coal Members that are commercially targeted for coalbed methane production in Indiana. On-line analyses of hydrocarbon gases methane to butanes (C1, C2, C3, n-C4, i-C4) and CO2 yielded gas concentrations, plus ??D and ??13C values. The low thermal maturity of Indiana coals with vitrinite reflectance R0 ??? 0.6% is in agreement with an overwhelmingly biogenic isotopic signature of coalbed gases containing ???96% methane generated via bacterial CO2-reduction. In contrast, thermogenic gas was generated in the stratigraphically equivalent coal beds in western Kentucky's Rough Creek Graben zone where higher maturities of up to R0 ??? 0.8% were reached owing to tectonic and hydrothermal activity. No secondary biogenic methane was observed in more mature western Kentucky coal beds where greater burial depth limits the recharge of meteoric water. Biogenic and thermogenic coalbed gases represent two end-members that are compositionally and isotopically distinct. Microbial biodegradation of thermogenic C2+ hydrocarbon gases in Indiana coal beds preferentially targets C3 and introduces isotope fractionation whereby remaining C3 is enriched in deuterium and 13C.

  19. Effect of acid rain on calcium carbonate saturation in the Albemarle sound of North Carolina

    SciTech Connect

    Rudolph, K.A.; Burgess, S.K.; Willey, J.D.; Kieber, R.J.

    1996-10-01

    The effects of acidic rainwater additions on calcium carbonate solubility and alkalinity in the poorly buffered, biologically active and commercially important waters of the Albemarle Sound, NC are reported. Samples collected monthly at four sites were analyzed for salinity, pK total alkalinity, and calcium concentrations. Five percent and 10% dilutions of sulfuric acid at pH 4, mimicking acid rain additions, were added and total alkalinity and calcium concentrations again determined. The addition of acid decreased the alkalinity in the Albemarle samples by as much as 15%, although the magnitude of the impact depended both on site and season. The effects of acid additions on dissolved calcium concentrations were more variable,. and also displayed a site and season dependency. Calcium concentrations, alkalinity, and pH values were also determined during controlled laboratory experiments, where 25 mg/L Callinectes sapidus shells were added to Albemarle Sound water. All three analytes increased significantly upon acid additions relative to controls.

  20. Simple quantification of surface carboxylic acids on chemically oxidized multi-walled carbon nanotubes

    NASA Astrophysics Data System (ADS)

    Gong, Hyejin; Kim, Seong-Taek; Lee, Jong Doo; Yim, Sanggyu

    2013-02-01

    The surface of multi-walled carbon nanotube (MWCNT) was chemically oxidized using nitric acid and sulfuric-nitric acid mixtures. Thermogravimetric analysis, transmission electron microscopy and infrared spectroscopy revealed that the use of acid mixtures led to higher degree of oxidation. More quantitative identification of surface carboxylic acids was carried out using X-ray photoelectron spectroscopy (XPS) and acid-base titration. However, these techniques are costly and require very long analysis times to promptly respond to the extent of the reaction. We propose a much simpler method using pH measurements and pre-determined pKa value in order to estimate the concentration of carboxylic acids on the oxidized MWCNT surfaces. The results from this technique were consistent with those obtained from XPS and titration, and it is expected that this simple quantification method can provide a cheap and fast way to monitor and control the oxidation reaction of MWCNT.

  1. Stable carbon isotopic compositions of organic acids in total suspended particles and dusts from Guangzhou, China

    NASA Astrophysics Data System (ADS)

    Ma, Shexia; Peng, Ping'an; Song, Jianzhong; Zhao, Jinping; He, Lulu; Sheng, Guoying; Fu, Jiamo

    2010-10-01

    Stable carbon isotopic compositions of individual organic acids were determined in total suspended particles and dusts from Guangzhou. The δ 13C values of high molecular weight n-alkanoic acids (C 20-C 28) varied from -34.1‰ to -32.4‰ and tended to be heavier in summer and lighter in winter. These δ 13C values indicate that high molecular weight n-alkanoic acids were derived mainly from emission by C 3 plants. Reduced biological synthesis of high molecular weight n-alkanoic acids in winter may be the reason for the light carbon isotopic composition. The δ 13C values of low molecular weight n-alkanoic acids (C 10-C 18) changed from -31.7‰ to -30.3‰ and exhibited a reverse seasonal trend, i.e., heavier in winter and lighter in summer. Slightly heavier δ 13C values of low molecular weight n-alkanoic acids than those of high molecular weight n-alkanoic acids suggested that they may be emitted from blended sources, e.g., anthropogenic sources and vegetation waxes. Lighter δ 13C values in summer may be attributed to relatively low anthropogenic sources and high botanic sources in summer. Dicarboxylic acids and aromatic acids have been proposed as secondary products from photochemical degradation. The average δ 13C values of dicarboxylic acids and aromatic acids were heavier, and ranged from -25.2‰ to -22.9‰ and from -30.0‰ to -27.6‰, respectively. Both dicarboxylic acids and aromatic acids displayed the same temporal variations in the δ 13C values, i.e., negative δ 13C in the summer samples and positive in the winter samples, which may be controlled by photochemical reactions; they are generally severe in winter in Guangzhou under the monsoon weather system. The heaviest δ 13C values were observed in dicarboxylic acids, indicating that dicarboxylic acids were formed by fast and more complete oxidation reactions. These results indicate that the stable carbon isotopic composition of organic acids may provide important information about sources and photochemical reactions of organic matter in the atmosphere.

  2. Carbon nanotubes as electronic interconnects in solid acid fuel cell electrodes.

    PubMed

    Varga, Áron; Pfohl, Moritz; Brunelli, Nicholas A; Schreier, Marcel; Giapis, Konstantinos P; Haile, Sossina M

    2013-10-01

    Carbon nanotubes have been explored as interconnects in solid acid fuel cells to improve the link between nanoscale Pt catalyst particles and macroscale current collectors. The nanotubes were grown by chemical vapor deposition on carbon paper substrates, using nickel nanoparticles as the catalyst, and were characterized using scanning electron microscopy and Raman spectroscopy. The composite electrode material, consisting of CsH2PO4, platinum nanoparticles, and platinum on carbon-black nanoparticles, was deposited onto the nanotube-overgrown carbon paper by electrospraying, forming a highly porous, fractal structure. AC impedance spectroscopy in a symmetric cell configuration revealed a significant reduction of the electrode impedance as compared to similarly prepared electrodes without carbon nanotubes. PMID:23942778

  3. On the neutralization of acid rock drainage by carbonate and silicate minerals

    NASA Astrophysics Data System (ADS)

    Sherlock, E. J.; Lawrence, R. W.; Poulin, R.

    1995-02-01

    The net result of acid-generating and-neutralizing reactions within mining wastes is termed acid rock drainage (ARD). The oxidation of sulfide minerals is the major contributor to acid generation. Dissolution and alteration of various minerals can contribute to the neutralization of acid. Definitions of alkalinity, acidity, and buffer capacity are reviewed, and a detailed discussion of the dissolution and neutralizing capacity of carbonate and silicate minerals related to equilibium conditions, dissolution mechanism, and kinetics is provided. Factors that determine neutralization rate by carbonate and silicate minerals include: pH, PCO 2, equilibrium conditions, temperature, mineral composition and structure, redox conditions, and the presence of foreign ions. Similar factors affect sulfide oxidation. Comparison of rates shows sulfides react fastest, followed by carbonates and silicates. The differences in the reaction mechanisms and kinetics of neutralization have important implications in the prediction, control, and regulation of ARD. Current static and kinetic prediction methods upon which mine permitting, ARD control, and mine closure plans are based do not consider sample mineralogy or the kinetics of the acid-generating and-neutralizing reactions. Erroneous test interpretations and predictions can result. The importance of considering mineralogy for site-specific interpretation is highlighted. Uncertainty in prediction leads to difficulties for the mine operator in developing satisfactory and cost-effective control and remediation measures. Thus, the application of regulations and guidelines for waste management planning need to beflexible.

  4. Efficient optical resolution of amino acid by alanine racemaze chiral analogue supported on mesoporous carbon

    NASA Astrophysics Data System (ADS)

    Jang, D.; Kim, K.; Park, D.; Kim, G.

    2012-09-01

    Optically pure D-amino acids are industrially important chiral building blocks for the synthesis of pharmaceuticals, food ingredients, and drug intermediates. Chemoenzymatic dynamic kinetic-resolution processes have recently been developed for deracemization of amino acids. S-ARCA would be a good candidate for the selective adsorption of D amino acid through the imine formation reaction. The organic phase containing S-ARCA adsorbent, TPPC or Ionic Liquid (as a phase transfer catalyst) in MC were coated on the surfaces of mesoporous carbon C-SBA-15(CMK). The aqueous solution of racemic D/L-amino acid and NaOH were added to the carbon support coated with ARCA. The D/L ratios on ARCA and in solution were determined with increasing reaction time. S-ARCA has a unique property for the selective adsorption of D- amino acid (up to 90% selcetivity) in the racemic mixture. The fixed bed reactor containing ARCA/carbon support was also adopted successfully for the selective separation of amino acid.

  5. Roles of sulfuric acid in elemental mercury removal by activated carbon and sulfur-impregnated activated carbon.

    PubMed

    Morris, Eric A; Kirk, Donald W; Jia, Charles Q; Morita, Kazuki

    2012-07-17

    This work addresses the discrepancy in the literature regarding the effects of sulfuric acid (H(2)SO(4)) on elemental Hg uptake by activated carbon (AC). H(2)SO(4) in AC substantially increased Hg uptake by absorption particularly in the presence of oxygen. Hg uptake increased with acid amount and temperature exceeding 500 mg-Hg/g-AC after 3 days at 200 C with AC treated with 20% H(2)SO(4). In the absence of other strong oxidizers, oxygen was able to oxidize Hg. Upon oxidation, Hg was more readily soluble in the acid, greatly enhancing its uptake by acid-treated AC. Without O(2), S(VI) in H(2)SO(4) was able to oxidize Hg, thus making it soluble in H(2)SO(4). Consequently, the presence of a bulk H(2)SO(4) phase within AC pores resulted in an orders of magnitude increase in Hg uptake capacity. However, the bulk H(2)SO(4) phase lowered the AC pore volume and could block the access to the active surface sites and potentially hinder Hg uptake kinetics. AC treated with SO(2) at 700 C exhibited a much faster rate of Hg uptake attributed to sulfur functional groups enhancing adsorption kinetics. SO(2)-treated carbon maintained its fast uptake kinetics even after impregnation by 20% H(2)SO(4). PMID:22681637

  6. 3-{[(Benzyloxy)carbonyl]amino}butanoic acid

    PubMed Central

    Kimino, Taira; Fujii, Isao

    2011-01-01

    In the title compound, C12H15NO4, the butyric acid group has a stretched trans conformation. The dihedral angle between the phenyl ring and the oxycarboxyamino N(C=O)OC plane is 56.6?(2). In the crystal, an inversion dimer is formed by a pair of OH?O hydrogen bonds. The dimers are further linked by NH?O hydrogen bonds between amide groups, forming a tape along the b axis. PMID:22058733

  7. Generation of aliphatic acid anions and carbon dioxide by hydrous pyrolysis of crude oils

    USGS Publications Warehouse

    Kharaka, Y.K.; Lundegard, P.D.; Ambats, G.; Evans, William C.; Bischoff, J.L.

    1993-01-01

    Two crude oils with relatively high (0.60 wt%) and low (0.18 wt%) oxygen contents were heated in the presence of water in gold-plated reactors at 300??C for 2348 h. The high-oxygen oil was also heated at 200??C for 5711 h. The compositions of aqueous organic acid anions of the oils and of the headspace gases were monitored inn order to investigate the distribution of organic acids that can be generated from liquid petroleum. The oil with higher oxygen content generated about five times as much organic anions as the other oil. The dominant organic anions produced were acetate, propionate and butyrate. Small amounts of formate, succinate, methyl succinate and oxalate were also produced. The dominant oxygen-containing product was CO2, as has been observed in similar studies on the hydrous pyrolysis of kerogen. These results indicate that a significant portion (10-30%) of organic acid anions reported i be generated by thermal alteration of oils in reservoir rocks. The bulk of organic acid anions present in formation waters, however, is most likely generated by thermal alteration of kerogen in source rocks. Kerogen is more abundant than oil in sedimentary basins and the relative yields of organic acid anions reported from the hydrous pyrolysis of kerogen are much higher than the yields obtained for the two oils. ?? 1993.

  8. Carbon Isotopic Measurements of Amino Acids in Stardust-Returned Samples

    NASA Technical Reports Server (NTRS)

    Elsila, Jamie

    2009-01-01

    NASA's Stardust spacecraft returned to Earth samples from comet 81P/Wild 2 in January 2006. Preliminary examinations revealed the presence of a suite of organic compounds including several amines and amino acids, but the origin of these compounds could not be identified. Here, we present the carbon isotopic ratios of glycine and e-aminocaproic acid (EACA), the two most abundant amino acids, in Stardust-returned foil samples measured by gas chromatography-combustion-isotope ratio mass spectrometry coupled with quadrupole mass spectrometry (GC-CAMS/IRMS).

  9. Carbon Isotopic Ratios of Amino Acids in Stardust-Returned Samples

    NASA Technical Reports Server (NTRS)

    Elsila, Jamie E.; Glavin, Daniel P.; Dworkin, Jason P.

    2009-01-01

    NASA's Stardust spacecraft returned to Earth samples from comet 81P/Wild 2 in January 2006. Preliminary examinations revealed the presence of a suite of organic compounds including several amines and amino acids, but the origin of these compounds could not be identified. Here. we present the carbon isotopic ratios of glycine and E-aminocaproic acid (EACH), the two most abundant amino acids observed, in Stardust-returned foil samples measured by gas chromatography-combustion-isotope ratio crass spectrometry coupled with quadrupole mass spectrometry (GC-QMS/IRMS).

  10. Variation in the Carbon Isotope Composition of a Plant with Crassulacean Acid Metabolism

    PubMed Central

    Lerman, J. C.; Deleens, Eliane; Nato, Aim; Moyse, Alexis

    1974-01-01

    The content of 13C varies in plants with Crassulacean acid metabolism. Differences up to 3.5 in the 13C/12C ratios were observed between leaves of different age in the same plant of Bryophyllum daigremontianum. Soluble and insoluble carbon in the same leaf differed up to 8, the largest difference occurring in the leaves with the highest Crassulacean acid metabolism activity. Models to account for the isotope discrimination by C3, C4, and Crassulacean acid metabolism plants are proposed. PMID:16658746

  11. Synergistic effect of self-assembled carboxylic acid-functionalized carbon nanotubes and carbon fiber for improved electro-activated polymeric shape-memory nanocomposite

    NASA Astrophysics Data System (ADS)

    Lu, Haibao; Min Huang, Wei

    2013-06-01

    The present work studies the synergistic effect of self-assembled carboxylic acid-functionalized carbon nanotube (CNT) and carbon fiber on the electrical property and electro-activated recovery behavior of shape memory polymer (SMP) nanocomposites. The combination of CNT and carbon fiber results in improved electrical conductivity in the SMP nanocomposites. Carboxylic acid-functionalized CNTs are grafted onto the carbon fibers and then self-assembled by deposition to significantly enhance the reliability of the bonding between carbon fiber and SMP via van der Waals and covalent crosslink. Furthermore, the self-assembled carboxylic acid-functionalized CNTs and carbon fibers enable the SMP nanocomposites for Joule heating triggered shape recovery.

  12. Modeling and optimizing the design of matrix treatments in carbonate reservoirs with self-diverting acid systems

    NASA Astrophysics Data System (ADS)

    Bulgakova, G. T.; Kharisov, R. Ya; Sharifullin, A. R.; Pestrikov, A. V.

    2015-01-01

    Application of a self-diverting-acid based on viscoelastic surfactant (SDVA) is a promising technology for improving the efficacy of acid treatment in oil and gas-bearing carbonate reservoirs. In this study, we present a mathematical model for assessing SDVA flow and reaction with carbonate rock using the SDVA rheological characteristics. The model calculates the technological parameters for acidizing operations and the prediction of well productivity after acid treatment, in addition to technical and economic optimization of the acidizing process by modeling different acid treatment options with varying volumes, injection rates, process fluids stages and initial economic scenarios.

  13. Reaction Mechanism for Direct Proton Transfer from Carbonic Acid to a Strong Base in Aqueous Solution I: Acid and Base Coordinate and Charge Dynamics.

    PubMed

    Daschakraborty, Snehasis; Kiefer, Philip M; Miller, Yifat; Motro, Yair; Pines, Dina; Pines, Ehud; Hynes, James T

    2016-03-10

    Protonation by carbonic acid H2CO3 of the strong base methylamine CH3NH2 in a neutral contact pair in aqueous solution is followed via Car-Parrinello molecular dynamics simulations. Proton transfer (PT) occurs to form an aqueous solvent-stabilized contact ion pair within 100 fs, a fast time scale associated with the compression of the acid-base hydrogen-bond (H-bond), a key reaction coordinate. This rapid barrierless PT is consistent with the carbonic acid-protonated base pKa difference that considerably favors the PT, and supports the view of intact carbonic acid as potentially important proton donor in assorted biological and environmental contexts. The charge redistribution within the H-bonded complex during PT supports a Mulliken picture of charge transfer from the nitrogen base to carbonic acid without altering the transferring hydrogen's charge from approximately midway between that of a hydrogen atom and that of a proton. PMID:26879554

  14. Vertically aligned carbon nanofiber electrode arrays for nucleic acid detection

    NASA Astrophysics Data System (ADS)

    Arumugam, Prabhu U.; Yu, Edmond; Riviere, Roger; Meyyappan, M.

    2010-10-01

    We present electrochemical detection of DNA targets that corresponds to Escherichia coli O157:H7 16S rRNA gene using a nanoelectrode array consisting of vertically aligned carbon nanofiber (VACNF) electrodes. Parylene C is used as gap filling 'matrix' material to avoid high temperature processing in electrode construction. This easy to deposit film of several micron heights provides a conformal coating between the high aspect ratio VACNFs with negligible pin-holes. The low background currents show the potential of this approach for ultra-sensitive detection. Consistent and reproducible electrochemical-signals are achieved using a simple electrode preparation. This simple, reliable and low-cost approach is a forward step in developing practical sensors for applications like pathogen detection, early cancer diagnosis and environmental monitoring.

  15. Microbial mediated formation of Fe-carbonate minerals under extreme acidic conditions.

    PubMed

    Snchez-Romn, Mnica; Fernndez-Remolar, David; Amils, Ricardo; Snchez-Navas, Antonio; Schmid, Thomas; San Martin-Uriz, Patxi; Rodrguez, Nuria; McKenzie, Judith A; Vasconcelos, Crisogono

    2014-01-01

    Discovery of Fe-carbonate precipitation in Rio Tinto, a shallow river with very acidic waters, situated in Huelva, South-western Spain, adds a new dimension to our understanding of carbonate formation. Sediment samples from this low-pH system indicate that carbonates are formed in physico-chemical conditions ranging from acid to neutral pH. Evidence for microbial mediation is observed in secondary electron images (Fig. 1), which reveal rod-shaped bacteria embedded in the surface of siderite nanocrystals. The formation of carbonates in Rio Tinto is related to the microbial reduction of ferric iron coupled to the oxidation of organic compounds. Herein, we demonstrate for the first time, that Acidiphilium sp. PM, an iron-reducing bacterium isolated from Rio Tinto, mediates the precipitation of siderite (FeCO3) under acidic conditions and at a low temperature (30C). We describe nucleation of siderite on nanoglobules in intimate association with the bacteria cell surface. This study has major implications for understanding carbonate formation on the ancient Earth or extraterrestrial planets. PMID:24755961

  16. Enhanced sidewall functionalization of single-wall carbon nanotubes using nitric acid.

    PubMed

    Tobias, Gerard; Shao, Lidong; Ballesteros, Belin; Green, Malcolm L H

    2009-10-01

    When a sample of as-made single-walled carbon nanotubes (SWNTs) is treated with nitric acid, oxidation debris are formed due to the functionalization (mainly carboxylation) of the amorphous carbon present in the sample and a continuous coating along the carbon nanotube walls is created preventing the sidewall functionalization of the SWNTs. This oxidation debris can be easily removed by an aqueous base wash leaving behind a sample with a low degree of functionality. After removal of the amorphous carbon (by steam purification) from a sample of as-made SWNTs, the resulting purified SWNTs are readily carboxylated on the walls by nitric acid treatment. The use of steam for the purification of SWNTs samples allows the removal of the amorphous carbon and graphitic layers coating the metal particles present in the sample without altering the tubular structure of the SWNTs. The exposed metal particles can then be easily removed by an acid wash. Comparison between the steam treatment and molten sodium hydroxide treatment is made. PMID:19908496

  17. Microbial mediated formation of Fe-carbonate minerals under extreme acidic conditions

    PubMed Central

    Sánchez-Román, Mónica; Fernández-Remolar, David; Amils, Ricardo; Sánchez-Navas, Antonio; Schmid, Thomas; Martin-Uriz, Patxi San; Rodríguez, Nuria; McKenzie, Judith A.; Vasconcelos, Crisogono

    2014-01-01

    Discovery of Fe-carbonate precipitation in Rio Tinto, a shallow river with very acidic waters, situated in Huelva, South-western Spain, adds a new dimension to our understanding of carbonate formation. Sediment samples from this low-pH system indicate that carbonates are formed in physico-chemical conditions ranging from acid to neutral pH. Evidence for microbial mediation is observed in secondary electron images (Fig. 1), which reveal rod-shaped bacteria embedded in the surface of siderite nanocrystals. The formation of carbonates in Rio Tinto is related to the microbial reduction of ferric iron coupled to the oxidation of organic compounds. Herein, we demonstrate for the first time, that Acidiphilium sp. PM, an iron-reducing bacterium isolated from Rio Tinto, mediates the precipitation of siderite (FeCO3) under acidic conditions and at a low temperature (30°C). We describe nucleation of siderite on nanoglobules in intimate association with the bacteria cell surface. This study has major implications for understanding carbonate formation on the ancient Earth or extraterrestrial planets. PMID:24755961

  18. Neutralizing Carbonic Acid in Deep Carbonate Strata below the North Atlantic

    SciTech Connect

    Daniel P. Schrag

    2005-12-01

    Our research is aimed at investigating several technical issues associated with carbon dioxide sequestration in calcium carbonate sediments below the sea floor through laboratory experiments and chemical transport modeling. Our goal is to evaluate the basic feasibility of this approach, including an assessment of optimal depths, sediment types, and other issues related to site selection. Through laboratory and modeling efforts, we are studying the flow of liquid carbon dioxide and carbon dioxide-water mixtures through calcium carbonate sediments to better understand the geomechanical and structural stability of the sediments during and after injection. Our modeling efforts in the first year show that the idea is feasible, but requires more sophisticated analysis of fluid flow at high pressure in deep sea sediments. In addition, we are investigating the kinetics of calcium carbonate dissolution in the presence of CO{sub 2}-water fluids, which is a critical feature of the system as it allows for increased permeability during injection. Our experimental results from the first year of work have shown that the kinetics are likely to be fast enough to create dissolution which will affect permeability. However, additional experiments are needed at high pressures, which will be a focus for years 2 and 3. We are also investigating the possibility of carbon dioxide hydrate formation in the pore fluid, which might complicate the injection procedure by reducing sediment permeability but might also provide an upper seal in the sediment-pore fluid system, preventing release of CO{sub 2} into the deep ocean, particularly if depth and temperature at the injection point rule out immediate hydrate formation. Finally, we are in the beginning stages of an economic analysis to estimate costs of drilling and gas injection, site monitoring as well as the availability of potential disposal sites with particular emphasis on those sites that are within the 200-mile economic zone of the United States.

  19. Interaction of organic acids with carbonate mineral surfaces in seawater and related solutions

    SciTech Connect

    Zullig, J.J.; Morse, J.W. )

    1988-06-01

    The adsorption of C{sub 4} to C{sub 18} fatty acid anion homologs from seawater and related solutions was examined on calcite, aragonite, dolomite and magnesite surfaces. Butyrate, octanoate and laurate did not adsorb, while myristate, palmitate and stearate absorbed on all carbonate surfaces. An increasing affinity for carbonate surfaces was found with increasing alkyl chain length for these fatty acids. Adsorption at low concentrations typical of marine waters is controlled by surface adsorption sites. At high concentration adsorption is governed by solution composition and limited by aqueous solubility. Adsorption-desorption reactions were characterized by a large resistant component that resulted in nonsingular isotherms. Myristate adsorption was enhanced in the presence of stearate cosorption. Orthophosphate in trace quantities was capable of displacing fatty acids from carbonate surfaces, but contrary to earlier studies, the authors found on major influence from magnesium ion on adsorption. The results of this study are interpreted in terms of a model based on the different types of forces which contribute to adsorption of these organic compounds. This model emphasizes the importance of organic aqueous solubility and the acid function as criteria controlling the adsorption of natural hydrophobic organics with carbonate mineral surfaces in aqueous fluids.

  20. Numbers of bacteria recovered from broiler carcasses and chiller water treated with hypochlorous and carbonic acids

    Technology Transfer Automated Retrieval System (TEKTRAN)

    A study was conducted to determine the effects of treating poultry chiller water with a mixture of hypochlorous and carbonic acids. Broiler carcasses and chiller water were obtained from a commercial processing facility which had recently installed a TOMCO Pathogen Management SystemJ to recycle wat...

  1. FATTY ACID STABLE ISOTOPE INDICATORS OF MICROBIAL CARBON SOURCE IN TROPICAL SOILS

    EPA Science Inventory

    The soil microbial community plays an important role in tropical ecosystem functioning because of its importance in the soil organic matter (SOM) cycle. We have measured the stable carbon isotopic ratio (delta13C) of individual phospholipid fatty acids (PLFAs) in a variety of tr...

  2. Polymerization of euphorbia oil with Lewis acid in carbon dioxide media

    Technology Transfer Automated Retrieval System (TEKTRAN)

    Boron trifluoride diethyl etherate (BF3-OEt2) Lewis acid catalyzed ring-opening polymerization of euphorbia oil (EO), a natural epoxy oil, in liquid carbon dioxide was conducted in an effort to develop useful vegetable oil based polymers. The resulting polymers (RPEO) were characterized by FTIR, 1H-...

  3. Titration of Monoprotic Acids with Sodium Hydroxide Contaminated by Sodium Carbonate.

    ERIC Educational Resources Information Center

    Michalowski, Tadeusz

    1988-01-01

    Discusses the effects of using carbon dioxide contaminated sodium hydroxide solution as a titrant for a solution of a weak monoprotic acid and the resulting distortion of the titration curve in comparison to one obtained when an uncontaminated titrant is used. (CW)

  4. EFFECT OF ACID TREATMENT ON DISSOLVED ORGANIC CARBON RETENTION BY A SPODIC HORIZON

    EPA Science Inventory

    Processes involving the movement of organic substances in forest soils are not well understood. This study was conducted to examine the role of acidic inputs on dissolved organic carbon (DOC) mobility, processes affecting the retention of DOV by a B horizon, and SO2-4 adsorption....

  5. From the First Measurements of Atmospheric Carbon Dioxide During the IGY to the Global Annual Greenhouse Gas Index in 2006: The Evolution of the Global Observing Network for Greenhouse Gases.

    NASA Astrophysics Data System (ADS)

    Hofmann, D. J.; Butler, J. H.; Dlugokencky, E. J.; Elkins, J. W.; Masarie, K.; Montzka, S. A.; Tans, P. P.

    2006-05-01

    During the International Geophysical Year, Dr. Charles "Dave" Keeling instituted both air sample collections at the South Pole in Antarctica and continuous carbon dioxide measurements with an infrared analyzer at the Mauna Loa Observatory in Hawaii. Both of these locations were later to become Observatories of the U.S. National Oceanic and Atmospheric Administration (NOAA), following its formation in 1970, and the pioneering measurements of Dave Keeling continued to be supported by NOAA at these sites until this day. In addition to instituting Observatories at key background locations (Pt. Barrow, Alaska; American Samoa; and more recently Trinidad Head, California, in addition to the Hawaii and Antarctic sites) the forerunners of NOAA/ESRL also began a global cooperative air sampling network in the late 1960's. The air samples were analyzed for carbon dioxide and other gases in the Boulder, Colorado laboratories. With the help of many people in many nations, this network has grown to the largest such effort in the world, numbering about 90 sites, including three ship routes, at present. In 1996, data from this network and from other networks around the world formed the basis of GLOBALVIEW, a web-based collection of carbon dioxide and methane data used extensively with transport models to determine global carbon dioxide sources and sinks. This data set is available at http://www.cmdl.noaa.gov/ccgg/globalview/index.html . In 2004, the global measurements of all the long-lived greenhouse gases, including carbon dioxide, methane, nitrous oxide, the chlorofluorocarbons, and ten minor halogen gases were condensed into a simple index, the "Annual Greenhouse Gas Index" (AGGI) by summing their radiative climate forcing since the pre-industrial era (taken as 1750). The NOAA AGGI is designed to enhance the connection between scientists and society by providing a normalized standard that can be easily understood and followed. The contribution of long-lived greenhouse gases to climate forcing is well understood by scientists and has been reported through a range of national and international assessments. Nevertheless, the language of scientists (for example, watts per square meter per year) often eludes policy makers, educators, and the general public. This index is designed to help bridge that gap.

  6. Carbon and hydrogen isotopic evidence for the origin of combustible gases in water-supply wells in north-central Pennsylvania

    USGS Publications Warehouse

    Révész, K. M.; Breen, K.J.; Baldassare, A.J.; Burruss, R.C.

    2010-01-01

    The origin of the combustible gases in groundwater from glacial-outwash and fractured-bedrock aquifers was investigated in northern Tioga County, Pennsylvania. Thermogenic methane (CH4) and ethane (C2H6) and microbial CH4 were found. Microbial CH4 is from natural in situ processes in the shale bedrock and occurs chiefly in the bedrock aquifer. The δ13C values of CH4 and C2H6 for the majority of thermogenic gases from water wells either matched or were between values for the samples of non-native storage-field gas from injection wells and the samples of gas from storage-field observation wells. Traces of C2H6 with microbial CH4 and a range of C and H isotopic compositions of CH4 indicate gases of different origins are mixing in sub-surface pathways; gas mixtures are present in groundwater. Pathways for gas migration and a specific source of the gases were not identified. Processes responsible for the presence of microbial gases in groundwater could be elucidated with further geochemical study.

  7. Acid rain damage to carbonate stone: a quantitative assessment based on the aqueous geochemistry of rainfall runoff from stone

    USGS Publications Warehouse

    Reddy, M.M.

    1988-01-01

    An onsite experimental procedure was used to identify and quantify acid rain damage to carbonate stone, based on the change in rain runoff chemical composition. Onsite data obtained during the summer and fall of 1984 at three locations in the northeastern United States indicate that carbonate stone surface recession is related to acid deposition. -from Author

  8. Nickel embedded in N-doped porous carbon for the hydrogenation of nitrobenzene to p-aminophenol in sulphuric acid.

    PubMed

    Wang, Tao; Dong, Zhen; Fu, Teng; Zhao, Yanchao; Wang, Tian; Wang, Yongzheng; Chen, Yi; Han, Baohang; Ding, Weiping

    2015-12-01

    An acid-resistant catalyst composed of nickel embedded in N-doped porous carbon is developed for the catalytic hydrogenation of nitrobenzene (NB) to p-aminophenol (PAP). The catalyst, due to a special electron donation from nickel to the N-doped porous carbon, shows an excellent catalytic performance and stability in sulphuric acid solution. PMID:26489366

  9. A Convenient Palladium-Catalyzed Carbonylative Suzuki Coupling of Aryl Halides with Formic Acid as the Carbon Monoxide Source.

    PubMed

    Qi, Xinxin; Jiang, Li-Bing; Li, Hao-Peng; Wu, Xiao-Feng

    2015-12-01

    A practical palladium-catalyzed carbonylative Suzuki coupling of aryl halides under carbon monoxide gas-free conditions has been developed. Here, formic acid was utilized as the carbon monoxide source for the first time with acetic anhydride as the additive. A variety of diarylketones were produced in moderate to excellent yields from the corresponding aryl halides and arylboronic acids. PMID:26486227

  10. 40 CFR 600.108-08 - Analytical gases.

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ... 40 Protection of Environment 31 2012-07-01 2012-07-01 false Analytical gases. 600.108-08 Section... ECONOMY AND GREENHOUSE GAS EXHAUST EMISSIONS OF MOTOR VEHICLES Fuel Economy and Carbon-Related Exhaust Emission Test Procedures 600.108-08 Analytical gases. The analytical gases for all fuel economy...

  11. 40 CFR 600.108-08 - Analytical gases.

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ... 40 Protection of Environment 30 2014-07-01 2014-07-01 false Analytical gases. 600.108-08 Section... ECONOMY AND GREENHOUSE GAS EXHAUST EMISSIONS OF MOTOR VEHICLES Fuel Economy and Carbon-Related Exhaust Emission Test Procedures 600.108-08 Analytical gases. The analytical gases for all fuel economy...

  12. 40 CFR 600.108-08 - Analytical gases.

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ... 40 Protection of Environment 31 2013-07-01 2013-07-01 false Analytical gases. 600.108-08 Section... ECONOMY AND GREENHOUSE GAS EXHAUST EMISSIONS OF MOTOR VEHICLES Fuel Economy and Carbon-Related Exhaust Emission Test Procedures 600.108-08 Analytical gases. The analytical gases for all fuel economy...

  13. Solubility of small-chain carboxylic acids in supercritical carbon dioxide

    SciTech Connect

    Sparks, Darrell L.; Estevez, L. Antonio; Hernandez, Rafael; McEwen, Jason; French, Todd

    2010-07-08

    The solubility of heptanoic acid and octanoic acid in supercritical carbon dioxide has been determined at temperatures of (313.15, 323.15, and 333.15) K over a pressure range of (8.5 to 30.0) MPa, depending upon the solute. The solubility of heptanoic acid ranged from a solute concentration of (0.08 ± 0.03) kg • m-3 (T = 323.15 K, p = 8.5 MPa) to (147 ± 0.2) kg • m-3 (T = 323.15 K, p = 20.0 MPa). The lowest octanoic acid solubility obtained was a solute concentration of (0.40 ± 0.1) kg • m-3 (T = 333.15 K, p = 10.0 MPa), while the highest solute concentration was (151 ± 2) kg • m-3 (T = 333.15 K, p = 26.7 MPa). In addition, solubility experiments were performed for nonanoic acid in supercritical carbon dioxide at 323.15 K and pressures of (10.0 to 30.0) MPa to add to the solubility data previously published by the authors. In general, carboxylic acid solubility increased with increasing solvent density. The results also showed that the solubility of the solutes decreased with increasing molar mass at constant supercritical-fluid density. Additionally, the efficacy of Chrastil's equation and other density-based models was evaluated for each fatty acid.

  14. Solubility of small-chain carboxylic acids in supercritical carbon dioxide

    DOE PAGESBeta

    Sparks, Darrell L.; Estevez, L. Antonio; Hernandez, Rafael; McEwen, Jason; French, Todd

    2010-07-08

    The solubility of heptanoic acid and octanoic acid in supercritical carbon dioxide has been determined at temperatures of (313.15, 323.15, and 333.15) K over a pressure range of (8.5 to 30.0) MPa, depending upon the solute. The solubility of heptanoic acid ranged from a solute concentration of (0.08 ± 0.03) kg • m-3 (T = 323.15 K, p = 8.5 MPa) to (147 ± 0.2) kg • m-3 (T = 323.15 K, p = 20.0 MPa). The lowest octanoic acid solubility obtained was a solute concentration of (0.40 ± 0.1) kg • m-3 (T = 333.15 K, p = 10.0more » MPa), while the highest solute concentration was (151 ± 2) kg • m-3 (T = 333.15 K, p = 26.7 MPa). In addition, solubility experiments were performed for nonanoic acid in supercritical carbon dioxide at 323.15 K and pressures of (10.0 to 30.0) MPa to add to the solubility data previously published by the authors. In general, carboxylic acid solubility increased with increasing solvent density. The results also showed that the solubility of the solutes decreased with increasing molar mass at constant supercritical-fluid density. Additionally, the efficacy of Chrastil's equation and other density-based models was evaluated for each fatty acid.« less

  15. Dissolution of single-walled carbon nanotubes in alkanol-cholic acid mixtures

    NASA Astrophysics Data System (ADS)

    Dyshin, A. A.; Eliseeva, O. V.; Bondarenko, G. V.; Kiselev, M. G.

    2015-09-01

    A procedure for dispersing the single-walled carbon nanotubes (SWCNTs) for preparing stable suspensions with high concentrations of individual nanotubes in various alcohols was described. The obtained suspensions were studied by Raman spectroscopy. The solubility of the single-walled carbon nanotubes in alcohols was found to depend on the concentration of cholic acid. The ethanol-surfactant mixture was shown to be the best solvent for all alkanol-cholic acid mixtures (0.018 mol/kg) under study used for preparing time-stable suspensions of single-walled carbon nanotubes. The dissolving ability of aliphatic alcohols was found to decrease in the series: ethanol-isopropanol- tert-butanol-butanol-propanol.

  16. Reporting emissions of greenhouse gases in Canada.

    PubMed

    Finlay, P; Stobbs, R

    1994-05-01

    Non-carbon dioxide greenhouse gases are considered in "Canada's National Report on Climate Change: Actions to Meet Commitments Under the United Nations Framework Convention on Climate Change". By including all major greenhouse gases and their anthropogenic sources and sinks using best available science, the Report provides a practical illustration of the "comprehensive approach" policy to implementing the Convention's requirements. In addition to carbon dioxide emissions from fossil fuel combustion, the Report includes information on other sources and sinks for carbon dioxide, and for methane and nitrous oxide. Other gases considered include polyflourocarbons, hydroflourocarbons, and the primary tropospheric ozone precursors, nitrogen oxides and volatile organic compounds. Current Global Warming Potential indices are used to compare and integrate the best estimates of climate change impacts of the major greenhouse gases. The presentation of emission data is intended to be transparent and comparable. The relative quality of the data for various gases and sources is indicated. The existence of environmental, economic, and other benefits to limiting emissions of all greenhouse gases, in addition to carbon dioxide, should be recognized. Continuing assessments and actions on non-carbon dioxide greenhouse gas emissions, both nationally and internationally, are suggested. PMID:24213890

  17. Stable carbon isotopic compositions of total carbon, dicarboxylic acids and glyoxylic acid in the tropical Indian aerosols: Implications for sources and photochemical processing of organic aerosols

    NASA Astrophysics Data System (ADS)

    Pavuluri, Chandra Mouli; Kawamura, Kimitaka; Swaminathan, T.; Tachibana, Eri

    2011-09-01

    The tropical Indian aerosols (PM10) collected on day- and nighttime bases in winter and summer, 2007 from Chennai (13.04N; 80.17E) were studied for stable carbon isotopic compositions (?13C) of total carbon (TC), individual dicarboxylic acids (C2-C9) and glyoxylic acid (?C2). ?13C values of TC ranged from -23.9 to -25.9 (-25.0 0.6; n = 49). Oxalic (C2) (-17.1 2.5), malonic (C3) (-20.8 1.8), succinic (C4) (-22.5 1.5) and adipic (C6) (-20.6 4.1) acids and ?C2 acid (-22.4 5.5) were found to be more enriched with 13C compared to TC. In contrast, suberic (C8) (-29.4 1.8), phthalic (Ph) (-30.1 3.5) and azelaic (C9) (-28.4 5.8) acids showed smaller ?13C values than TC. Based on comparisons of ?13C values of TC in Chennai aerosols to those (-24.7 2.2) found in unburned cow-dung samples collected from Chennai and isotopic signatures of the particles emitted from point sources, we found that biofuel/biomass burning are the major sources of carbonaceous aerosols in South and Southeast Asia. The decrease in ?13C values of C9 diacid by about 5 from winter to summer suggests that tropical plant emissions also significantly contribute to organic aerosol in this region. Significant increase in ?13C values from C4 to C2 diacids in Chennai aerosols could be attributed for their photochemical processing in the tropical atmosphere during long-range transport from source regions.

  18. Improving stable carbon and oxygen isotope geochemical measurements in dolomite: reference material and acid fractionation factor

    NASA Astrophysics Data System (ADS)

    Vandeginste, V.; John, C. M.; Jourdan, A.; Davis, S.

    2010-12-01

    The analysis of stable carbon and oxygen isotope composition is one of the most commonly used techniques in stratigraphic and diagenetic research of carbonate rocks. The wide-spread use and easy access of this long-established method has the side effect that little attention is paid to fundamental calibrations. Dolomite is often measured against a calcite standard (NBS19), and the acid fractionation factor used to calibrate is based on the one for calcite. To date, no reference material exists for dolomite. In this study, which is part of dolomite research in the Qatar Carbonates and Carbon Storage Research Centre project, we focus on two main goals. First, we characterize a current standard of dolomite used for major and minor elemental geochemistry, and assess its suitability as a new dolomite standard for ?18O and ?13C. Second, we attempt to better constrain the acid fractionation factor for dolomite and assess the influence of different dolomite types on this fractionation factor. As only two third of the total oxygen in the carbonate is released in the form of CO2 during acid reaction, a fractionation between the reacting carbonate and the resulting gas will occur. A recent study by Kim et al. (2007) improved on the acid fractionation factors for calcite and aragonite. Often, the acid fractionation factor for dolomite is used to calculate ?18O and ?13C from the values obtained by calibration with the calcite standard. Only two studies (from the 1980s) have attempted to constrain the acid fractionation factor for dolomite, of which only Rosenbaum and Sheppard (1986) did experiments not only at 25C, but also at 50 and 100C. The dataset of the latter authors is, however, very limited and contains only two dolomite samples. We aim at improving the constraints on the acid fractionation factor of dolomite by reacting a wide range of different types of dolomite at a wide range of acid temperature, and compare this to the absolute isotopic composition of the samples measured on a fluorination line.

  19. Prolonged acid rain facilitates soil organic carbon accumulation in a mature forest in Southern China.

    PubMed

    Wu, Jianping; Liang, Guohua; Hui, Dafeng; Deng, Qi; Xiong, Xin; Qiu, Qingyan; Liu, Juxiu; Chu, Guowei; Zhou, Guoyi; Zhang, Deqiang

    2016-02-15

    With the continuing increase in anthropogenic activities, acid rain remains a serious environmental threat, especially in the fast developing areas such as southern China. To detect how prolonged deposition of acid rain would influence soil organic carbon accumulation in mature subtropical forests, we conducted a field experiment with simulated acid rain (SAR) treatments in a monsoon evergreen broadleaf forest at Dinghushan National Nature Reserve in southern China. Four levels of SAR treatments were set by irrigating plants with water of different pH values: CK (the control, local lake water, pH≈4.5), T1 (water pH=4.0), T2 (water pH=3.5), and T3 (water pH=3.0). Results showed reduced pH measurements in the topsoil exposed to simulated acid rains due to soil acidification. Soil respiration, soil microbial biomass and litter decomposition rates were significantly decreased by the SAR treatments. As a result, T3 treatment significantly increased the total organic carbon by 24.5% in the topsoil compared to the control. Furthermore, surface soil became more stable as more recalcitrant organic matter was generated under the SAR treatments. Our results suggest that prolonged acid rain exposure may have the potential to facilitate soil organic carbon accumulation in the subtropical forest in southern China. PMID:26657252

  20. Culture strategies for lipid production using acetic acid as sole carbon source by Rhodosporidium toruloides.

    PubMed

    Huang, Xiang-Feng; Liu, Jia-Nan; Lu, Li-Jun; Peng, Kai-Ming; Yang, Gao-Xiang; Liu, Jia

    2016-04-01

    Rhodosporidium toruloides AS 2.1389 was tested using different concentrations of acetic acid as a low-cost carbon source for the production of microbial lipids, which are good raw materials for biodiesel production. It grew and had higher lipid contents in media containing 4-20g/L acetic acid as the sole carbon source, compared with that in glucose-containing media under the same culture conditions. At acetic acid concentrations as high as 20g/L and the optimal carbon-to-nitrogen ratio (C/N) of 200 in a batch culture, the highest biomass production was 4.35g/L, with a lipid content of 48.2%. At acetic acid concentrations as low as 4g/L, a sequencing batch culture (SBC) with a C/N of 100 increased biomass production to 4.21g/L, with a lipid content of 38.6%. These results provide usable culture strategies for lipid production by R. toruloides AS 2.1389 when using diverse waste-derived volatile fatty acids. PMID:26851898

  1. The healing effect of stearic acid applied on amorphous carbon film with dispersed nanodiamonds

    NASA Astrophysics Data System (ADS)

    Yamazaki, T.; Shoji, K.; Ikeshoji, T.-T.; Suzumura, A.

    2012-08-01

    Diamond-like carbon (DLC) films have been shown to improve the friction and wear properties of applications with severe loads. Hydrogenated amorphous carbon films (a-C:H), a type of DLC film, were coated onto 440C stainless steel disk surfaces. The plasma enhanced chemical vapour deposition method was used as a coating process, and nanodiamond (ND) particles were dispersed into the film during the deposition process. Stearic acid was expected to affect the lubricating properties of the film because of its reported effectiveness on diamond surfaces. A lubricated reciprocal sliding friction test with 10,000 cycles confirmed that stearic acid improved the friction and wear properties of the ND dispersed a-C:H film. Furthermore, film wear caused by a sliding test without stearic acid could be healed by sliding with stearic acid as long as the level of critical damage was not reached. Raman spectra for the worn tracks revealed the healing effect of the stearic acid on the film because the spectra for the worn tracks after 10,000 cycles were identical to those of the control film, which was not worn. In contrast, the spectra for the worn tracks or debris showed a broad D band peak and no G peak, which was consistent with disordered amorphous carbon.

  2. Synthesis of sulfonated porous carbon nanospheres solid acid by a facile chemical activation route

    NASA Astrophysics Data System (ADS)

    Chang, Binbin; Guo, Yanzhen; Yin, Hang; Zhang, Shouren; Yang, Baocheng

    2015-01-01

    Generally, porous carbon nanospheres materials are usually prepared via a template method, which is a multi-steps and high-cost strategy. Here, we reported a porous carbon nanosphere solid acid with high surface area and superior porosity, as well as uniform nanospheical morphology, which prepared by a facile chemical activation with ZnCl2 using resorcinol-formaldehyde (RF) resins spheres as precursor. The activation of RF resins spheres by ZnCl2 at 400 °C brought high surface area and large volume, and simultaneously retained numerous oxygen-containing and hydrogen-containing groups due to the relatively low processing temperature. The presence of these functional groups is favorable for the modification of -SO3H groups by a followed sulfonation treating with sulphuric acid and organic sulfonic acid. The results of N2 adsorption-desorption and electron microscopy clearly showed the preservation of porous structure and nanospherical morphology. Infrared spectra certified the variation of surface functional groups after activation and the successful modification of -SO3H groups after sulfonation. The acidities of catalysts were estimated by an indirect titration method and the modified amount of -SO3H groups were examined by energy dispersive spectra. The results suggested sulfonated porous carbon nanospheres catalysts possessed high acidities and -SO3H densities, which endowed their significantly catalytic activities for biodiesel production. Furthermore, their excellent stability and recycling property were also demonstrated by five consecutive cycles.

  3. Adsorption equilibrium, kinetics and thermodynamics of dichloroacetic acid from aqueous solution using mesoporous carbon.

    PubMed

    Ding, Ying; Zhu, Jianzhong; Cao, Yang; Chen, Shenglu

    2014-08-01

    The presence of disinfection by-products, such as trihalomethanes and haloacetic acids in water, is believed to be harmful to human health. In this work, mesoporous carbon was synthesized with the evaporation-induced self-assembly method and employed to evaluate the effects of initial concentration, contact time, pH and temperature on the removal of dichloroacetic acid in batch experiments. Adsorption equilibrium was established in 480 min and the maximum adsorption (350mg/g) of dichloroacetic acid on the mesoporous carbon was observed to occur at 308 K and pH 3.0. Freundlich and Langmuir isotherms were used to analyse the equilibrium data at different temperatures; kinetic data were fitted to the pseudo-first-order and pseudo-second-order models and found that the adsorption capacity, mass transfer coefficient and diffusivity of dichloroacetic acid were directly affected by the physical and chemical parameters. In addition, the various thermodynamic parameters, such as Gibbs free energy (Delta G), enthalpy (Delta H = 54.35 kJmol-1) and entropy (Delta S = 258.36 Jmol-1 K-1) were calculated to analyse the adsorption process. The experimental results indicated that the mesoporous carbon was an excellent adsorbent for dichloroacetic acid removal from aqueous solutions. PMID:24956790

  4. [Studies on carbonization of saccharides by using aqueous solution of various acids].

    PubMed

    Zhang, Xin; He, An-Qi; Kang, Ting-Guo; Xia, Jin-Ming; Weng, Shi-Fu; Xu, Yi-Zhuang; Wu, Jin-Guang

    2014-09-01

    The authors tried to establish an approach to use acids to convert biomass into a fuel with higher carbon content and lower oxygen content in a zero-energy-consumption fashion. Considering that biomass is composed of monosaccharide, we used aqueous solutions of variation acids including hydrochloric acid, sulfuric acid and perchloric acid to treat 2-deoxy-ribose and fructose at ambient temperature and pressure. Black substances were produced after a period of time when 2-deoxy-ribose and fructose were mixed with aqueous solutions containing 8 mol L(-1) acids. The black substance was collected and characterized by using elemental analysis, Fourier transform infrared spectroscopy (FTIR) and X-ray photoelectron spectroscopy (XPS). Elemental analysis results indicate that the contents of carbon increases significantly in the black substances in comparison with 2-deoxy-ribose and fructose. Moreover, XPS results indicate that the content of oxygen in the black substance undergoes a significant decrease compared with pure 2-deoxy-ribose and fructose. In the XPS spectra, the is peaks of 2-deoxy-ribose, strong sub peak at 286. 05 eV, which is assigned to carbon linked to oxygen directly, dominate in the C is peak envelop. After treatment by HClO4, the peak decreased dramatically. This result also supports the conclusion that the content of oxygen in mono-saccharide is significantly reduced after treatment by acids. In the FTIR spectra of the black substances, strong peaks can be observed around 1 600 cm(-1), indicating that C==C bond is formed in the product. The above results suggest that treatments with acids may be developed as a new zero-energy-consumption approach to convert biomass in a new fuel with improved energy output efficiency. PMID:25532323

  5. Controlled exposures of volunteers to respirable carbon and sulfuric acid aerosols

    SciTech Connect

    Anderson, K.R.; Avol, E.L.; Edwards, S.A.; Shamoo, D.A.; Ruchuan Peng; Linn, W.S.; Hackney, J.D. )

    1992-06-01

    Respirable carbon or fly ash particles are suspected to increase the respiratory toxicity of coexisting acidic air pollutants, by concentrating acid on their surfaces and so delivering it efficiently to the lower respiratory tract. To investigate this issue, the authors exposed 15 healthy and 15 asthmatic volunteers in a controlled-environment chamber to four test atmospheres: (1) clean air; (2) 0.5-{mu}m H{sub 2}SO{sub 4} aerosol at {approx}100 {mu}g/m{sup 3}, generated from water solution; (3) 0.5-{mu}m carbon aerosol at {approx}250 {mu}g/m{sup 3}, generated from highly pure carbon black with specific surface area comparable to ambient pollution particles; and (4) carbon as in (3) plus {approx}100 {mu}g/m{sup 3} of ultrafine H{sub 2}SO{sub 4} aerosol generated from fuming sulfuric acid. Electron microscopy showed that nearly all acid in (4) became attached to carbon particle surfaces, and that most particles remained in the sub-{mu}m size range. Exposures were performed double-blind, 1 week apart. They lasted 1 hr each, with alternate 10-min periods of heavy exercise (ventilation {approx}50 L/min) and rest. Subjects gargled citrus juice before exposure to suppress airway ammonia. Lung function and symptoms were measured pre-exposure, after initial exercise, and at end-exposure. Bronchial reactivity to methacholine was measured after exposure. Statistical analyses tested for effects of H{sub 2}SO{sub 4} or carbon, separate or interactive, on health measures.

  6. Carbonate precipitation under bulk acidic conditions as a potential biosignature for searching life on Mars

    NASA Astrophysics Data System (ADS)

    Fernández-Remolar, David C.; Preston, Louisa J.; Sánchez-Román, Mónica; Izawa, Matthew R. M.; Huang, L.; Southam, Gordon; Banerjee, Neil R.; Osinski, Gordon R.; Flemming, Roberta; Gómez-Ortíz, David; Prieto Ballesteros, Olga; Rodríguez, Nuria; Amils, Ricardo; Darby Dyar, M.

    2012-10-01

    Recent observations of carbonate minerals in ancient Martian rocks have been interpreted as evidence for the former presence of circumneutral solutions optimal for carbonate precipitation. Sampling from surface and subsurface regions of the low-pH system of Río Tinto has shown, unexpectedly, that carbonates can form under diverse macroscopic physicochemical conditions ranging from very low to neutral pH (1.5-7.0). A multi-technique approach demonstrates that carbonate minerals are closely associated with microbial activity. Carbonates occur in the form of micron-size carbonate precipitates under bacterial biofilms, mineralization of subsurface colonies, and possible biogenic microstructures including globules, platelets and dumbbell morphologies. We propose that carbonate precipitation in the low-pH environment of Río Tinto is a process enabled by microbially-mediated neutralization driven by the reduction of ferric iron coupled to the oxidation of biomolecules in microbially-maintained circumneutral oases, where the local pH (at the scale of cells or cell colonies) can be much different than in the macroscopic environment. Acidic conditions were likely predominant in vast regions of Mars over the last four billion years of planetary evolution. Ancient Martian microbial life inhabiting low-pH environments could have precipitated carbonates similar to those observed at Río Tinto. Preservation of carbonates at Río Tinto over geologically significant timescales suggests that similarly-formed carbonate minerals could also be preserved on Mars. Such carbonates could soon be observed by the Mars Science Laboratory, and by future missions to the red planet.

  7. Matrix Isolation Studies of Carbonic AcidThe Vapor Phase above the ?-Polymorph

    PubMed Central

    2013-01-01

    Twenty years ago two different polymorphs of carbonic acid, ?- and ?-H2CO3, were isolated as thin, crystalline films. They were characterized by infrared and, of late, by Raman spectroscopy. Determination of the crystal structure of these two polymorphs, using cryopowder and thin film X-ray diffraction techniques, has failed so far. Recently, we succeeded in sublimating ?-H2CO3 and trapping the vapor phase in a noble gas matrix, which was analyzed by infrared spectroscopy. In the same way we have now investigated the ?-polymorph. Unlike ?-H2CO3, ?-H2CO3 was regarded to decompose upon sublimation. Still, we have succeeded in isolation of undecomposed carbonic acid in the matrix and recondensation after removal of the matrix here. This possibility of sublimation and recondensation cycles of ?-H2CO3 adds a new aspect to the chemistry of carbonic acid in astrophysical environments, especially because there is a direct way of ?-H2CO3 formation in space, but none for ?-H2CO3. Assignments of the FTIR spectra of the isolated molecules unambiguously reveal two different carbonic acid monomer conformers (C2v and Cs). In contrast to the earlier study on ?-H2CO3, we do not find evidence for centrosymmetric (C2h) carbonic acid dimers here. This suggests that two monomers are entropically favored at the sublimation temperature of 250 K for ?-H2CO3, whereas they are not at the sublimation temperature of 210 K for ?-H2CO3. PMID:23631554

  8. Collagen tissue treated with chitosan solutions in carbonic acid for improved biological prosthetic heart valves.

    PubMed

    Gallyamov, Marat O; Chaschin, Ivan S; Khokhlova, Marina A; Grigorev, Timofey E; Bakuleva, Natalia P; Lyutova, Irina G; Kondratenko, Janna E; Badun, Gennadii A; Chernysheva, Maria G; Khokhlov, Alexei R

    2014-04-01

    Calcification of bovine pericardium dramatically shortens typical lifetimes of biological prosthetic heart valves and thus precludes their choice for younger patients. The aim of the present work is to demonstrate that the calcification is to be mitigated by means of treatment of bovine pericardium in solutions of chitosan in carbonic acid, i.e. water saturated with carbon dioxide at high pressure. This acidic aqueous fluid unusually combines antimicrobial properties with absolute biocompatibility as far as at normal pressure it decomposes spontaneously and completely into H2O and CO2. Yet, at high pressures it can protonate and dissolve chitosan materials with different degrees of acetylation (in the range of 16-33%, at least) without any further pretreatment. Even exposure of the bovine pericardium in pure carbonic acid solution without chitosan already favours certain reduction in calcification, somewhat improved mechanical properties, complete biocompatibility and evident antimicrobial activity of the treated collagen tissue. The reason may be due to high extraction ability of this peculiar compressed fluidic mixture. Moreover, exposure of the bovine pericardium in solutions of chitosan in carbonic acid introduces even better mechanical properties and highly pronounced antimicrobial activity of the modified collagen tissue against adherence and biofilm formation of relevant Gram-positive and Gram-negative strains. Yet, the most important achievement is the detected dramatic reduction in calcification for such modified collagen tissues in spite of the fact that the amount of the thus introduced chitosan is rather small (typically ca. 1wt.%), which has been reliably detected using original tritium labelling method. We believe that these improved properties are achieved due to particularly deep and uniform impregnation of the collagen matrix with chitosan from its pressurised solutions in carbonic acid. PMID:24582232

  9. Hydrogen-bond acidic functionalized carbon nanotubes (CNTs) with covalently-bound hexafluoroisopropanol groups

    SciTech Connect

    Fifield, Leonard S.; Grate, Jay W.

    2010-06-01

    Fluorinated hydrogen-bond acidic groups are directly attached to the backbone of single walled carbon nanotubes (SWCNTs) without the introduction of intermediate electron donating surface groups. Hexafluoroalcohol functional groups are exceptionally strong hydrogen bond acids, and are added to the nanotube surface using the aryl diazonium approach to create hydrogen-bond acidic carbon nanotube (CNT) surfaces. These groups can promote strong hydrogen-bonding interactions with matrix materials in composites or with molecular species to be concentrated and sensed. In the latter case, this newly developed material is expected to find useful application in chemical sensors and in CNT-based preconcentrator devices for the detection of pesticides, chemical warfare agents and explosives.

  10. An amperometric uric acid biosensor based on chitosan-carbon nanotubes electrospun nanofiber on silver nanoparticles.

    PubMed

    Numnuam, Apon; Thavarungkul, Panote; Kanatharana, Proespichaya

    2014-06-01

    A novel amperometric uric acid biosensor was fabricated by immobilizing uricase on an electrospun nanocomposite of chitosan-carbon nanotubes nanofiber (Chi-CNTsNF) covering an electrodeposited layer of silver nanoparticles (AgNPs) on a gold electrode (uricase/Chi-CNTsNF/AgNPs/Au). The uric acid response was determined at an optimum applied potential of -0.35V vs Ag/AgCl in a flow-injection system based on the change of the reduction current for dissolved oxygen during oxidation of uric acid by the immobilized uricase. The response was directly proportional to the uric acid concentration. Under the optimum conditions, the fabricated uric acid biosensor had a very wide linear range, 1.0-400?molL(-1), with a very low limit of detection of 1.0?molL(-1) (s/n?=?3). The operational stability of the uricase/Chi-CNTsNF/AgNPs/Au biosensor (up to 205 injections) was excellent and the storage life was more than six weeks. A low Michaelis-Menten constant of 0.21mmolL(-1) indicated that the immobilized uricase had high affinity for uric acid. The presence of potential common interfering substances, for example ascorbic acid, glucose, and lactic acid, had negligible effects on the performance of the biosensor. When used for analysis of uric acid in serum samples, the results agreed well with those obtained by use of the standard enzymatic colorimetric method (P?>?0.05). PMID:24718436

  11. Facile Carbon Fixation to Performic Acids by Water-Sealed Dielectric Barrier Discharge.

    PubMed

    Kawasaki, Mitsuo; Morita, Tatsuo; Tachibana, Kunihide

    2015-01-01

    Carbon fixation refers to the conversion of carbon dioxide (CO2) to organic materials, as commonly performed in nature through photosynthesis by plants and other autotrophic organisms. The creation of artificial carbon fixation processes is one of the greatest challenges for chemistry to solve the critical environmental issue concerning the reduction of CO2 emissions. We have developed an electricity-driven facile CO2 fixation process that yields performic acid, HCO2OH, from CO2 and water at neutral pH by dielectric barrier discharge with an input electric power conversion efficiency of currently 0.2-0.4%. This method offers a promising future technology for artificial carbon fixation on its own, and may also be scaled up in combination with e.g., the post-combustion CO2 capture and storage technology. PMID:26439402

  12. Facile Carbon Fixation to Performic Acids by Water-Sealed Dielectric Barrier Discharge

    PubMed Central

    Kawasaki, Mitsuo; Morita, Tatsuo; Tachibana, Kunihide

    2015-01-01

    Carbon fixation refers to the conversion of carbon dioxide (CO2) to organic materials, as commonly performed in nature through photosynthesis by plants and other autotrophic organisms. The creation of artificial carbon fixation processes is one of the greatest challenges for chemistry to solve the critical environmental issue concerning the reduction of CO2 emissions. We have developed an electricity-driven facile CO2 fixation process that yields performic acid, HCO2OH, from CO2 and water at neutral pH by dielectric barrier discharge with an input electric power conversion efficiency of currently 0.2−0.4%. This method offers a promising future technology for artificial carbon fixation on its own, and may also be scaled up in combination with e.g., the post-combustion CO2 capture and storage technology. PMID:26439402

  13. Facile Carbon Fixation to Performic Acids by Water-Sealed Dielectric Barrier Discharge

    NASA Astrophysics Data System (ADS)

    Kawasaki, Mitsuo; Morita, Tatsuo; Tachibana, Kunihide

    2015-10-01

    Carbon fixation refers to the conversion of carbon dioxide (CO2) to organic materials, as commonly performed in nature through photosynthesis by plants and other autotrophic organisms. The creation of artificial carbon fixation processes is one of the greatest challenges for chemistry to solve the critical environmental issue concerning the reduction of CO2 emissions. We have developed an electricity-driven facile CO2 fixation process that yields performic acid, HCO2OH, from CO2 and water at neutral pH by dielectric barrier discharge with an input electric power conversion efficiency of currently 0.2-0.4%. This method offers a promising future technology for artificial carbon fixation on its own, and may also be scaled up in combination with e.g., the post-combustion CO2 capture and storage technology.

  14. One carbon metabolism in anaerobic bacteria: Regulation of carbon and electron flow during organic acid production

    SciTech Connect

    Zeikus, J.G.; Jain, M.K.

    1992-01-01

    This reporting period, progress is reported on the following: metabolic pathway of solvent production in B. methylotrophicum; the biochemical mechanism for metabolic regulation of the succinate fermentation; models to understand the physiobiochemical function of formate metabolism in anaerobes and; models for understanding the influence of low pH on one carbon metabolism. (CBS)

  15. Neutralizing Carbonic Acid in Deep Carbonate Strata below the North Atlantic

    SciTech Connect

    Daniel P. Schrag

    2006-07-14

    Our research is aimed at investigating several technical issues associated with carbon dioxide sequestration in calcium carbonate sediments below the sea floor through laboratory experiments and chemical transport modeling. Our goal is to evaluate the basic feasibility of this approach, including an assessment of optimal depths, sediment types, and other issues related to site selection. The results of our modeling efforts were published this past summer in the Proceedings of the National Academy of Sciences. We are expanding on that work through a variety of laboratory and modeling efforts. In the laboratories at Columbia and at Harvard, we are studying the flow of liquid carbon dioxide and carbon dioxide-water mixtures through calcium carbonate sediments to better understand the geomechanical and structural stability of the sediments during and after injection. We are currently preparing the results of these findings for publication. In addition, we are investigating the kinetics of calcium carbonate dissolution in the presence of CO{sub 2}-water fluids, which is a critical feature of the system as it allows for increased permeability during injection. We are also investigating the possibility of carbon dioxide hydrate formation in the pore fluid, which might complicate the injection procedure by reducing sediment permeability but might also provide an upper seal in the sediment-pore fluid system, preventing release of CO{sub 2} into the deep ocean, particularly if depth and temperature at the injection point rule out immediate hydrate formation. This is done by injecting liquid CO{sub 2} into various types of porous media, and then monitoring the changes in permeability. Finally, we are performing an economic analysis to estimate costs of drilling and gas injection, site monitoring as well as the availability of potential disposal sites with particular emphasis on those sites that are within the 200-mile economic zone of the United States. We present some preliminary results from these analyses. A paper discussing the site selection based on data from the Ocean Drilling Program and Deep Sea Drilling Program is currently in preparation.

  16. Ozonation of naphthalenesulphonic acid in the aqueous phase in the presence of basic activated carbons.

    PubMed

    Rivera-Utrilla, J; Snchez-Polo, M

    2004-10-12

    The present study aimed to explore the possibility of increasing the purification efficacy of ozone in the removal of high-toxicity contaminants by using carbons of basic character and to analyze the mechanism involved in this process. These carbons were prepared by treating a commercial activated carbon (Witco, W) with ammonia (W-A), ammonium carbonate (W-C), or urea (W-U), under high pressure and temperature. The ammonia and carbonate treatments slightly increased the mesoporosity and, to a greater degree, the macroporosity of carbon W, whereas the urea treatment produced an increase in the porosity across the whole range of pore sizes. In addition, treatment of the activated carbon with these nitrogenating agents produced a marked change in the chemical nature of its surface. Thus, according to the pH of the point of zero charge (pHPZC) values obtained for each sample, carbon W was neutral (pHPZC = 7.12), but the treated carbons were basic, especially carbon W-U (pHPZC = 8.85). This basicity results from an increased concentration of basic oxygenated and nitrogenated surface functional groups, as confirmed by the results of elemental and XPS analyses. An increase in the degradation of 1,3,6-naphthalenetrisulfonic acid was observed when the activated carbon samples were added to the system. This degradation was especially enhanced in the presence of carbon W-U. The increased NTS degradation rate in the presence of the activated carbon is due to an increased concentration of highly reactive radicals in the system. When the catalytic activity of the activated carbon samples was related to their chemical and textural characteristics, it was found that: (i) The catalytic activity increased with an increase in the surface basicity. Interestingly, in the sample with greatest catalytic activity in NTS ozonation, carbon W-U, most of the nitrogenated surface groups introduced were pyrrol groups. These groups increase the electronic density of the basal plane of the activated carbon, thereby enhancing the reduction of ozone on the surface and the generation of highly reactive radicals in the system. (ii) The greater catalytic activity of carbon W-U may also be partly related to its greater surface area and higher volume of mesopores and macropores; these large pores facilitate access of the ozone to the surface active centers of the carbon, increasing its catalytic activity. The presence of the activated carbon samples during NTS ozonation also favored the removal of total organic carbon present in the solution, due to (a) transformation of organic matter into CO2 through the generation of highly reactive species catalyzed by the presence of the activated carbons (catalytic contribution) and (b) adsorption of NTS oxidation byproducts on the activated carbon (adsorptive contribution). The results obtained show that activated carbons treated with nitrogenating agents are very promising catalysts for application in the ozonation of aromatic compounds. PMID:15461509

  17. AIE luminogen-functionalised mesoporous nanomaterials for efficient detection of volatile gases.

    PubMed

    Li, Dongdong; Zhang, Yuping; Fan, Zhiying; Yu, Jihong

    2015-09-18

    Mesoporous silica nanoparticles functionalised with aggregation-induced emission (AIE) luminogen via a carbon-nitrogen double bond are fabricated into films by a dip-coating method. The as-made films can serve as efficient fluorescent sensors for the naked-eye detection of volatile acid gases by colour and emission changes, as well as for the detection of 2,4-dinitrotoluene vapours by fluorescence quenching. PMID:26234409

  18. [Effects of simulated acid rain on decomposition of soil organic carbon and crop straw].

    PubMed

    Zhu, Xue-Zhu; Huang, Yao; Yang, Xin-Zhong

    2009-02-01

    To evaluate the effects of acid rain on the organic carbon decomposition in different acidity soils, a 40-day incubation test was conducted with the paddy soils of pH 5.48, 6.70 and 8.18. The soils were amended with 0 and 15 g x kg(-1) of rice straw, adjusted to the moisture content of 400 g x kg(-1) air-dried soil by using simulated rain of pH 6.0, 4.5, and 3.0, and incubated at 20 degrees C. The results showed that straw, acid rain, and soil co-affected the CO2 emission from soil system. The amendment of straw increased the soil CO2 emission rate significantly. Acid rain had no significant effects on soil organic carbon decomposition, but significantly affected the straw decomposition in soil. When treated with pH 3.0 acid rain, the amount of decomposed straw over 40-day incubation in acid (pH 5.48) and alkaline (pH 8.18) soils was 8% higher, while that in neutral soil (pH 6.70) was 15% lower, compared to the treatment of pH 6.0 rain. In the treatment of pH 3.0 acid rain, the decomposition rate of soil organic C in acid (pH 5.48) soil was 43% and 50% (P < 0.05) higher than that in neutral (pH 6.70) and alkaline (pH 8.18) soils, while the decomposition rate of straw in neutral soil was 17% and 16% (P < 0.05) lower than that in acid and alkaline soils, respectively. PMID:19459394

  19. Ancient low–molecular-weight organic acids in permafrost fuel rapid carbon dioxide production upon thaw

    PubMed Central

    Drake, Travis W.; Wickland, Kimberly P.; Spencer, Robert G. M.; McKnight, Diane M.; Striegl, Robert G.

    2015-01-01

    Northern permafrost soils store a vast reservoir of carbon, nearly twice that of the present atmosphere. Current and projected climate warming threatens widespread thaw of these frozen, organic carbon (OC)-rich soils. Upon thaw, mobilized permafrost OC in dissolved and particulate forms can enter streams and rivers, which are important processors of OC and conduits for carbon dioxide (CO2) to the atmosphere. Here, we demonstrate that ancient dissolved organic carbon (DOC) leached from 35,800 y B.P. permafrost soils is rapidly mineralized to CO2. During 200-h experiments in a novel high–temporal-resolution bioreactor, DOC concentration decreased by an average of 53%, fueling a more than sevenfold increase in dissolved inorganic carbon (DIC) concentration. Eighty-seven percent of the DOC loss to microbial uptake was derived from the low–molecular-weight (LMW) organic acids acetate and butyrate. To our knowledge, our study is the first to directly quantify high CO2 production rates from permafrost-derived LMW DOC mineralization. The observed DOC loss rates are among the highest reported for permafrost carbon and demonstrate the potential importance of LMW DOC in driving the rapid metabolism of Pleistocene-age permafrost carbon upon thaw and the outgassing of CO2 to the atmosphere by soils and nearby inland waters. PMID:26504243

  20. Ancient low-molecular-weight organic acids in permafrost fuel rapid carbon dioxide production upon thaw.

    PubMed

    Drake, Travis W; Wickland, Kimberly P; Spencer, Robert G M; McKnight, Diane M; Striegl, Robert G

    2015-11-10

    Northern permafrost soils store a vast reservoir of carbon, nearly twice that of the present atmosphere. Current and projected climate warming threatens widespread thaw of these frozen, organic carbon (OC)-rich soils. Upon thaw, mobilized permafrost OC in dissolved and particulate forms can enter streams and rivers, which are important processors of OC and conduits for carbon dioxide (CO2) to the atmosphere. Here, we demonstrate that ancient dissolved organic carbon (DOC) leached from 35,800 y B.P. permafrost soils is rapidly mineralized to CO2. During 200-h experiments in a novel high-temporal-resolution bioreactor, DOC concentration decreased by an average of 53%, fueling a more than sevenfold increase in dissolved inorganic carbon (DIC) concentration. Eighty-seven percent of the DOC loss to microbial uptake was derived from the low-molecular-weight (LMW) organic acids acetate and butyrate. To our knowledge, our study is the first to directly quantify high CO2 production rates from permafrost-derived LMW DOC mineralization. The observed DOC loss rates are among the highest reported for permafrost carbon and demonstrate the potential importance of LMW DOC in driving the rapid metabolism of Pleistocene-age permafrost carbon upon thaw and the outgassing of CO2 to the atmosphere by soils and nearby inland waters. PMID:26504243

  1. The adsorption of gold, palladium and platinum from acidic chloride solutions on mesoporous carbons.

    SciTech Connect

    Zalupski, Peter R.; McDowell, Rocklan; Dutech, Guy

    2014-08-05

    Studies on the adsorption characteristics of gold, palladium and platinum on mesoporous carbon (CMK-3) and sulfur-impregnated mesoporous carbon (CMK-3/S) evaluated the benefits/drawbacks of the presence of a layer of elemental sulfur inside mesoporous carbon structures. Adsorption isotherms collected for Au(III), Pd(II) and Pt(IV) on those materials suggest that sulfur does enhance the adsorption of those metal ions in mildly acidic environment (pH 3). The isotherms collected in 1 M HCl show that the benefit of sulfur disappears due to the competing influence of large concentration of hydrogen ions on the ion-exchanging mechanism of metal ions sorption on mesoporous carbon surfaces. The collected acid dependencies illustrate similar adsorption characteristics for CMK-3 and CMK-3/S in 1-5 M HCl concentration range. Sorption of metal ions from diluted aqueous acidic mixtures of actual leached electronic waste demonstrated the feasibility of recovery of gold from such liquors.

  2. The adsorption of gold, palladium and platinum from acidic chloride solutions on mesoporous carbons.

    DOE PAGESBeta

    Zalupski, Peter R.; McDowell, Rocklan; Dutech, Guy

    2014-08-05

    Studies on the adsorption characteristics of gold, palladium and platinum on mesoporous carbon (CMK-3) and sulfur-impregnated mesoporous carbon (CMK-3/S) evaluated the benefits/drawbacks of the presence of a layer of elemental sulfur inside mesoporous carbon structures. Adsorption isotherms collected for Au(III), Pd(II) and Pt(IV) on those materials suggest that sulfur does enhance the adsorption of those metal ions in mildly acidic environment (pH 3). The isotherms collected in 1 M HCl show that the benefit of sulfur disappears due to the competing influence of large concentration of hydrogen ions on the ion-exchanging mechanism of metal ions sorption on mesoporous carbon surfaces.more » The collected acid dependencies illustrate similar adsorption characteristics for CMK-3 and CMK-3/S in 1-5 M HCl concentration range. Sorption of metal ions from diluted aqueous acidic mixtures of actual leached electronic waste demonstrated the feasibility of recovery of gold from such liquors.« less

  3. The adsorption of gold, palladium and platinum from acidic chloride solutions on mesoporous carbons.

    SciTech Connect

    Peter Zalupski; Rocklan McDowell; Guy Dutech

    2014-10-01

    Studies on the adsorption characteristics of gold, palladium and platinum on mesoporous carbon (CMK-3) and sulfur-impregnated mesoporous carbon (CMK-3/S) evaluated the benefits/drawbacks of the presence of a layer of elemental sulfur inside mesoporous carbon structures. Adsorption isotherms collected for Au(III), Pd(II) and Pt(IV) on those materials suggest that sulfur does enhance the adsorption of those metal ions in mildly acidic environment (pH 3). The isotherms collected in 1 M HCl show that the benefit of sulfur disappears due to the competing influence of large concentration of hydrogen ions on the ion-exchanging mechanism of metal ions sorption on mesoporous carbon surfaces. The collected acid dependencies illustrate similar adsorption characteristics for CMK-3 and CMK-3/S in 1-5 M HCl concentration range. Sorption of metal ions from diluted aqueous acidic mixtures of actual leached electronic waste demonstrated the feasibility of recovery of gold from such liquors.

  4. AIR INFILTRATION MEASUREMENTS USING TRACER GASES: A LITERATURE REVIEW

    EPA Science Inventory

    The report gives results of a literature review of air filtration measurements using tracer gases, including sulfur hexafluoride, hydrogen, carbon monoxide, carbon dioxide, nitrous oxide, and radioactive argon and krypton. Sulfur hexafluoride is the commonest tracer gas of choice...

  5. Design and synthesis of palladium/graphitic carbon nitride/carbon black hybrids as high-performance catalysts for formic acid and methanol electrooxidation

    NASA Astrophysics Data System (ADS)

    Qian, Huayu; Huang, Huajie; Wang, Xin

    2015-02-01

    Here we report a facile two-step method to synthesize high-performance palladium/graphitic carbon nitride/carbon black (Pd/g-C3N4/carbon black) hybrids for electrooxidizing formic acid and methanol. The coating of g-C3N4 on carbon black surface is realized by a low-temperature heating treatment, followed by the uniform deposition of palladium nanoparticles (Pd NPs) via a wet chemistry route. Owning to the significant synergistic effects of the individual components, the preferred Pd/g-C3N4/carbon black electrocatalyst exhibits exceptional forward peak current densities as high as 2155 and 1720 mA mg-1Pd for formic acid oxidation in acid media and methanol oxidation in alkaline media, respectively, far outperforming the commercial Pd-C catalyst. The catalyst also shows reliable stability, demonstrating that the newly-designed hybrids have great promise in constructing high-performance portable fuel cell systems.

  6. Fabrication and characterization of polylactic acid and polylactic acid/multi-walled carbon nanotube nanofibers through centrifugal spinning

    NASA Astrophysics Data System (ADS)

    Patlan, Richard

    Biocompatible polymer nanofibers hold great potential in the biomedical engineering field. Their biodegradable nature and enhanced properties could help solve a wide array of health related problems, particularly in the areas of tissue regeneration, drug delivery, and biosensor design. The novel Forcespinning method allows the production of submicron fibers without many of the drawbacks found in electrospinning, while also providing a substantial increase in fiber production. The aim of the study was to utilize this method to fabricate non-woven nanofibrous mats composed of polylactic acid (PLA) and polylactic acid/multi-walled carbon nanotube composite fibers. The morphology, thermal properties, and crystalline structure of the resulting nanofibers were then characterized using Scanning Electron Microscopy (SEM), Transmission Electron Microscopy (TEM), Thermogravimetric Analysis (TGA), Differential Scanning Calorimetry (DSC), and X-Ray Diffraction (XRD).

  7. Trehalose 6-phosphate coordinates organic and amino acid metabolism with carbon availability.

    PubMed

    Figueroa, Carlos M; Feil, Regina; Ishihara, Hirofumi; Watanabe, Mutsumi; Kölling, Katharina; Krause, Ursula; Höhne, Melanie; Encke, Beatrice; Plaxton, William C; Zeeman, Samuel C; Li, Zhi; Schulze, Waltraud X; Hoefgen, Rainer; Stitt, Mark; Lunn, John E

    2016-02-01

    Trehalose 6-phosphate (Tre6P) is an essential signal metabolite in plants, linking growth and development to carbon metabolism. The sucrose-Tre6P nexus model postulates that Tre6P acts as both a signal and negative feedback regulator of sucrose levels. To test this model, short-term metabolic responses to induced increases in Tre6P levels were investigated in Arabidopsis thaliana plants expressing the Escherichia coli Tre6P synthase gene (otsA) under the control of an ethanol-inducible promoter. Increased Tre6P levels led to a transient decrease in sucrose content, post-translational activation of nitrate reductase and phosphoenolpyruvate carboxylase, and increased levels of organic and amino acids. Radio-isotope ((14) CO2 ) and stable isotope ((13) CO2 ) labelling experiments showed no change in the rates of photoassimilate export in plants with elevated Tre6P, but increased labelling of organic acids. We conclude that high Tre6P levels decrease sucrose levels by stimulating nitrate assimilation and anaplerotic synthesis of organic acids, thereby diverting photoassimilates away from sucrose to generate carbon skeletons and fixed nitrogen for amino acid synthesis. These results are consistent with the sucrose-Tre6P nexus model, and implicate Tre6P in coordinating carbon and nitrogen metabolism in plants. PMID:26714615

  8. Trihalomethane formation potential of aquatic and terrestrial fulvic and humic acids: Sorption on activated carbon.

    PubMed

    Abouleish, Mohamed Y Z; Wells, Martha J M

    2015-07-15

    Humic substances (HSs) are precursors for the formation of hazardous disinfection by-products (DBPs) during chlorination of water. Various surrogate parameters have been used to investigate the generation of DBPs by HS precursors and the removal of these precursors by activated carbon treatment. Dissolved organic carbon (DOC)- and ultraviolet absorbance (UVA254)-based isotherms are commonly reported and presumed to be good predictors of the trihalomethane formation potential (THMFP). However, THMFP-based isotherms are rarely published such that the three types of parameters have not been compared directly. Batch equilibrium experiments on activated carbon were used to generate constant-initial-concentration sorption isotherms for well-characterized samples obtained from the International Humic Substances Society (IHSS). HSs representing type (fulvic acid [FA], humic acid [HA]), origin (aquatic, terrestrial), and geographical source (Nordic, Suwannee, Peat, Soil) were examined at pH6 and pH9. THMFP-based isotherms were generated and compared to determine if DOC- and UVA254-based isotherms were good predictors of the THMFP. The sorption process depended on the composition of the HSs and the chemical nature of the activated carbon, both of which were influenced by pH. Activated carbon removal of THM-precursors was pH- and HS-dependent. In some instances, the THMFP existed after UVA254 was depleted. PMID:25847173

  9. Effect of acid treatment on dissolved organic carbon retention by a spodic horizon

    SciTech Connect

    Vance, G.F.; David, M.B.

    1989-01-01

    Processes involving the movement of organic substances in forest soils are not well understood. The study was conducted to examine the role of acidic inputs on dissolved organic carbon (DOC) mobility, processes affecting the retention of DOC by a B horizon, and SO4(2-) adsorption. Using O and B horizon samples from a Spodosol collected in a forested watershed in Maine, acid solutions leached through O, B, and O over B(O/B) soils in small vacuum extractor columns were analyzed for DOC, DOC fractions, and anions. For the O and O/B columns, DOC in the leachates decreased (7550 to 3350 and 2380 to 850 micro mol C/L, respectively) with an increase in acidic inputs; for the B horizon, the reverse was the case (435 to 1570 micro mol C/L). The DOC in leachates from the O horizon was dominated by hydrophobic and hydrophilic acids (68 and 20% of DOC with no acid addition), which were altered by acidic inputs (46 and 36% of DOC at p(H(1+))=2). The hydrophobic acid percentage in leachates from O/B horizon columns decreased from 52 to 28%, whereas hydrophilic acids increased from 27 to 47% with H2O and p(H(1+))=2 treatments, respectively. Ionic strength adjustment (I=0.01) of treatment solutions reduced C solubilization in O and O/B horizon leachates, leading to lower DOC leaching.

  10. ESTERIFICATION OF OLEIC ACID IN SUPERCRITICAL CARBON DIOXIDE CATALYZED BY FUNCTIONALIZED MESOPOROUS SILICA AND AN IMMOBILIZED LIPASE

    Technology Transfer Automated Retrieval System (TEKTRAN)

    Organosulfonic acid-functionalized mesoporous silicas were tested for catalytic performance in the esterification of oleic acid with methanol in flowing supercritical carbon dioxide. The energy of activation of the sulfonic acid catalysts was found to be about 42 kJ/mol and was shown to be independ...

  11. Colloidal methods for the fabrication of carbon nanotube-manganese dioxide and carbon nanotube-polypyrrole composites using bile acids.

    PubMed

    Ata, M S; Zhitomirsky, I

    2015-09-15

    Nature inspired strategies have been developed for the colloidal processing of advanced composites for supercapacitor applications. New approach was based on the use of commercially available bile acid salts, such as sodium cholate (ChNa) and taurocholic acid sodium salt (TChNa). It was demonstrated that cholic acid (ChH) films can be obtained by electrophoretic deposition (EPD) from ChNa solutions. The analysis of deposition yield, quartz crystal microbalance and cyclic voltammetry data provided an insight into the anodic deposition mechanism. The outstanding suspension stability of multiwalled carbon nanotubes (MWCNT), achieved using bile acids as anionic dispersants, allowed the fabrication of MWCNT films by EPD. The use of ChNa for EPD offered advantages of binding and film forming properties of this material. Composite MnO2-MWCNT films, prepared using ChNa as a dispersant and film forming agent for EPD, showed promising capacitive behavior. In another colloidal strategy, TChNa was used as a dispersant for MWCNT for the fabrication of polypyrrole (PPy) coated MWCNT. The use of PPy coated MWCNT allowed the fabrication of electrodes with high active mass loading, high capacitance and excellent capacitance retention at high charge-discharge rates. PMID:26001135

  12. Selective Acidic Leaching of Spent Zinc-Carbon Batteries Followed by Zinc Electrowinning

    NASA Astrophysics Data System (ADS)

    Shalchian, Hossein; Rafsanjani-Abbasi, Ali; Vahdati-Khaki, Jalil; Babakhani, Abolfazl

    2015-02-01

    In this work, a selective acidic leaching procedure was employed for recycling zinc from spent zinc-carbon batteries. Leaching experiments were carried out in order to maximize zinc recovery and minimize manganese recovery in diluted sulfuric acid media. Response surface methodology and analysis of variance were employed for experimental design, data analysis, and leaching optimization. The experimental design has 28 experiments that include 24 main runs and four replicate in center point. The optimal conditions obtained from the selective acidic leaching experiments, were sulfuric acid concentration of 1 pct v/v, leaching temperature of 343 K (70 C), pulp density of 8 pct w/v, and stirring speed of 300 rpm. The results show that the zinc and manganese recoveries after staged selective leaching are about 92 and 15 pct, respectively. Finally, metallic zinc with purity of 99.9 pct and electrolytic manganese dioxide were obtained by electrowinning.

  13. Extraction of palladium from acidic solutions with the use of carbon adsorbents

    SciTech Connect

    O.N. Kononova; N.G. Goryaeva; N.B. Dostovalova; S.V. Kachin; A.G. Kholmogorov

    2007-08-15

    We studied the sorption of palladium(II) on LKAU-4, LKAU-7, and BAU carbon adsorbents from model hydrochloric acid solutions and the solutions of spent palladium-containing catalysts. It was found that sorbents based on charcoal (BAU) and anthracite (LKAU-4) were characterized by high sorption capacities for palladium. The kinetics of the saturation of carbon adsorbents with palladium(II) ions was studied, and it was found that more than 60% of the initial amount of Pd(II) was recovered in a 1-h contact of an adsorbent with a model solution. This value for the solutions of spent catalysts was higher than 35%.

  14. The erosion of carbonate stone by acid rain: Laboratory and field investigations

    SciTech Connect

    Baedecker, P.A. ); Reddy, M.M. )

    1993-02-01

    This paper describes a laboratory experiment on the effects of acidic deposition on carbonate stone erosion. It can serve as the basis for an undergraduate (or pre college) experiment in environmental chemistry. Recent field investigations are described that provide measurements of carbonate stone dissolution and mechanical erosion under weathering conditions that are prevalent in the eastern US. The purpose of the laboratory work is to answer questions concerning the effects of hydrogen ion deposition on stone erosion processes that were difficult to resolve on the basis of field experiments alone.

  15. Microwave-assisted polyol synthesis of carbon nitride dots from folic acid for cell imaging

    PubMed Central

    Guan, Weiwei; Gu, Wei; Ye, Ling; Guo, Chenyang; Su, Su; Xu, Pinxiang; Xue, Ming

    2014-01-01

    A green, one-step microwave-assisted polyol synthesis was employed to prepare blue luminescent carbon nitride dots (CNDs) using folic acid molecules as both carbon and nitrogen sources. The as-prepared CNDs had an average size of around 4.51 nm and could be well dispersed in water. Under excitation at 360 nm, the CNDs exhibited a strong blue luminescence and the quantum yield was estimated to be 18.9%, which is greater than that of other reported CNDs. Moreover, the CNDs showed low cytotoxicity and could efficiently label C6 glioma cells, demonstrating their potential in cell imaging. PMID:25382977

  16. Process characterization and influence of alternative carbon sources and carbon-to-nitrogen ratio on organic acid production by Aspergillus oryzae DSM1863.

    PubMed

    Ochsenreither, Katrin; Fischer, Christian; Neumann, Anke; Syldatk, Christoph

    2014-06-01

    L-Malic acid and fumaric acid are C4 dicarboxylic organic acids and considered as promising chemical building blocks. They can be applied as food preservatives and acidulants in rust removal and as polymerization starter units. Molds of the genus Aspergillus are able to produce malic acid in large quantities from glucose and other carbon sources. In order to enhance the production potential of Aspergillus oryzae DSM 1863, production and consumption rates in an established bioreactor batch-process based on glucose were determined. At 35 C, up to 42 g/L malic acid was produced in a 168-h batch process with fumaric acid as a by-product. In prolonged shaking flask experiments (353 h), the suitability of the alternative carbon sources xylose and glycerol at a carbon-to-nitrogen (C/N) ratio of 200:1 and the influence of different C/N ratios in glucose cultivations were tested. When using glucose, 58.2 g/L malic acid and 4.2 g/L fumaric acid were produced. When applying xylose or glycerol, both organic acids are produced but the formation of malic acid decreased to 45.4 and 39.4 g/L, respectively. Whereas the fumaric acid concentration was not significantly altered when cultivating with xylose (4.5 g/L), it is clearly enhanced by using glycerol (9.3 g/L). When using glucose as a carbon source, an increase or decrease of the C/N ratio did not influence malic acid production but had an enormous influence on fumaric acid production. The highest fumaric acid concentrations were determined at the highest C/N ratio (300:1, 8.44 g/L) and lowest at the lowest C/N ratio (100:1, 0.7 g/L). PMID:24604500

  17. Optimization of modified carbon paste electrode with multiwalled carbon nanotube/ionic liquid/cauliflower-like gold nanostructures for simultaneous determination of ascorbic acid, dopamine and uric acid.

    PubMed

    Afraz, Ahmadreza; Rafati, Amir Abbas; Najafi, Mojgan

    2014-11-01

    We describe the modification of a carbon paste electrode (CPE) with multiwalled carbon nanotubes (MWCNTs) and an ionic liquid (IL). Electrochemical studies by using a D-optimal mixture design in Design-Expert software revealed an optimized composition of 60% graphite, 14.2% paraffin, 10.8% MWCNT and 15% IL. The optimal modified CPE shows good electrochemical properties that are well matched with model prediction parameters. In the next step, the optimized CPE was modified with gold nanostructures by applying a double-pulse electrochemical technique. The resulting electrode was characterized by scanning electron microscopy, energy dispersive X-ray spectroscopy, X-ray diffraction, and electrochemical impedance spectroscopy. It gives three sharp and well-separated oxidation peaks for ascorbic acid (AA), dopamine (DA), and uric acid (UA). The sensor enables simultaneous determination of AA, DA and UA with linear responses from 0.3 to 285, 0.08 to 200, and 0.1 to 450 ?M, respectively, and with 120, 30 and 30 nM detection limits (at an S/N of 3). The method was successfully applied to the determination of AA, DA, and UA in spiked samples of human serum and urine. PMID:25280680

  18. Photocatalytic degradation of L-acid by TiO2 supported on the activated carbon.

    PubMed

    Wang, Yu-Ping; Wang, Lian-Jun; Peng, Pan-Ying

    2006-01-01

    TiO2 sol was prepared by sol-gel technique with tetrabutyl titanate as precursor. Supported TiO2 catalysts on activated carbon were prepared by soak and sintering method. The aggregation of nano-TiO2 particles can be effectively suppressed by added polyethylene glycol (PEG) as a surface modifier. The average particle diameter of TiO2, specific surface area and absorbability of catalyst can be modified. Based on characteristics of the TiO2 photocatalyst with XRD, specific surface area, adsorption valves of methylene blue and the amount of TiO2 supported on the activated carbon, the photocatalytic degradation of L-acid was studied. The effect of the factors, such as pH of the solution, the initial concentration of L-acid on the photocatalytic degradation of L-acid, were studied also. It was found that when the pH of the solution is 1.95, the amount of photocatalyst is 0.5 g, the concentration of the L-acid solution is 1.34 x 10(-3) mol/L and the illumination time is 7 h, the photocatalytic degradation efficiency of L-acid can reach 89.88%. The catalyst was reused 6 times and its degradation efficiency hardly changed. PMID:17294657

  19. Characterization of nano-lead-doped active carbon and its application in lead-acid battery

    NASA Astrophysics Data System (ADS)

    Hong, Bo; Jiang, Liangxing; Xue, Haitao; Liu, Fangyang; Jia, Ming; Li, Jie; Liu, Yexiang

    2014-12-01

    In this paper, nano-lead-doped active carbon (nano-Pb/AC) composite with low hydrogen evolution current for lead-acid battery was prepared by ultrasonic-absorption and chemical-precipitate method. The nano-Pb/AC composite was characterized by SEM, EDS and TEM. The electrochemical characterizations are performed by linear sweep voltammetry (LSV), electrochemical impedance spectroscopy (EIS) and cyclic voltammetry (CV) in a three-electrode system. Since intermediate adsorption is the rate-determining step, the hydrogen evolution reaction (HER) is markedly inhibited as the intermediate adsorption impedance of nano-Pb/AC increased. Meanwhile, the working potential of nano-Pb/AC is widened to the whole potential region of Pb negative plate (from -1.36 V to -0.86 V vs. Hg/HgSO4) in lead-acid battery. In addition, nano-Pb can improve the interfacial compatibility between AC and Pb paste, accordingly relieve the symptoms of carbon floatation. Finally, 2.0 V single-cell flooded lead-acid batteries with 1.0 wt.% nano-Pb/AC or 1.0 wt.% AC addition in negative active materials are assembled. The cell performances test results show that the 3 h rate capacity, quick charging performance, high current discharging performance and cycling performance of nano-Pb/AC modified battery are all improved compared with regular lead-acid battery and AC modified lead-acid battery.

  20. Methods for estimation of long-term non-carbonate neutralisation of acid rock drainage.

    PubMed

    Miller, Stuart D; Stewart, Warwick S; Rusdinar, Yuni; Schumann, Russell E; Ciccarelli, Joseph M; Li, Jun; Smart, Roger St C

    2010-04-01

    In the long-term phase of an acid rock drainage (ARD) evolution profile, after any short-term neutralisation capacity provided by carbonate minerals is exhausted, the net acid release is a product of a declining acid generation rate (AGR) and a slower, long-term acid neutralisation rate mainly provided by gangue silicate minerals. At some point, the AGR and the non-carbonate acid neutralisation rate (ANRnc) will be similar. Matching of the AGR and ANRnc near 10mg H(2)SO(4)/kg/week is demonstrated in data from 10-year columns. This long-term neutralisation is not measured at present in any accepted assessment tests. Methods to estimate ANRnc, based on silicate mineralogy and solution assays from long-term column leach tests, are compared. Good agreement is demonstrated between rates measured from the solution assay data and those calculated from mineralogy using kinetic databases. More rigorous analysis of the leachate chemistry of selected long-term leach tests also suggests possible cover design criteria based on the maximum AGR that will maintain a pH>4 in leachate from ARD materials. The data show a distinct break at an AGR of 3mg H(2)SO(4)/kg/week, below which no leachate pH is less than 4. The results indicate that an AGR of 10t H(2)SO(4)/ha/year is conservative and a suitable cover design target for ARD control that would be matched by ANRnc. PMID:20097405

  1. Electrochemical and XPS studies of decylamides of ?-amino acids adsorption on carbon steel in acidic environment

    NASA Astrophysics Data System (ADS)

    Olivares, O.; Likhanova, N. V.; Gmez, B.; Navarrete, J.; Llanos-Serrano, M. E.; Arce, E.; Hallen, J. M.

    2006-02-01

    Corrosion inhibition of steel in hydrochloric acid by decylamides of ?-amino acids derivatives was studied using gravimetric and electrochemical techniques. Protection efficiencies of 90% were obtained with 100 ppm of tyrosine and glycine derivatives, while alanine and valine derivatives reached only 80%. The order of increasing inhibition efficiency was correlated with the modification of the molecular structure of inhibitors. Potentiodynamic polarization curves indicated that both the decylamide of tyrosine and glycine acted primarily as anodic type inhibitors, whereas the decylamide of alanine and valine were of the cathodic type. Thermodynamic parameters and Flory-Huggins adsorption isotherms described the experimental findings. The number of active sites, equilibrium constant, enthalpy and change of free energy were computed for all inhibitors studied. This information suggested that organic molecules were adsorbed and displaced water molecules from the steel surface. X-ray photoelectron spectroscopy confirmed that species of N, C and O interacted with steel to form a continuous protective film.

  2. Evaluation of the Giggenbach bottle method using artificial fumarolic gases

    NASA Astrophysics Data System (ADS)

    Lee, S.; Jeong, H. Y.

    2013-12-01

    Volcanic eruption is one of the most dangerous natural disasters. Mt. Baekdu, located on the border between North Korea and China, has been recently showing multiple signs of its eruption. The magmatic activity of a volcano strongly affects the composition of volcanic gases, which can provide a useful tool for predicting the eruption. Among various volcanic gas monitoring methods, the Giggenbach bottle method involves the on-site sampling of volcanic gases and the subsequent laboratory analysis, thus making it possible to detect a range of volcanic gases at low levels. In this study, we aim to evaluate the effectiveness of the Giggenbach bottle method and develop the associated analytical tools using artificial fumarolic gases with known compositions. The artificial fumarolic gases are generated by mixing CO2, CO, H2S, SO2, Ar, and H2 gas streams with a N2 stream sparged through an acidic medium containing HCl and HF. The target compositions of the fumarolic gases are selected to cover those reported for various volcanoes under different tectonic environments as follows: CO2 (2-12 mol %), CO (0.3-1 mol %), H2S (0.7-2 mol %), SO2 (0.6-4 mol %), Ar (0.3-0.7 mol %), H2 (0.3-0.7 mol %), HCl (0.2-1 mol %), and HF (< 0.015 mol %). The artificial fumarolic gases are collected into an evacuated bottle partially filled with 4 M NaOH solution containing 0.5 mM Cd(CH3COO)2. While non-condensable components such as CO, Ar, H2, and N2 accumulate in the headspace of the bottle, acidic components including CO2, SO2, HCl, and HF dissolve into the alkaline solution. In case of H2S, it reacts with dissolved Cd2+ to precipitate as CdS(s). The gas accumulated in the headspace can be analyzed for CO, Ar, H2, and N2 on a gas chromatography. The alkaline solution is first separated from yellowish CdS precipitates by filtration, and then pretreated with hydrogen peroxide to oxidize dissolved SO2 (H2SO3) to SO42-. The resultant solution can be analyzed for SO2 as SO42-, HCl as Cl-, and HF as F- on an ion chromatography and CO2 on an ionic carbon analyzer. Also, the amount of H2S can be determined by measuring the remaining dissolved Cd2+ on an inductively coupled plasma-mass spectrometry.

  3. Conducting Carbon Dot-Polypyrrole Nanocomposite for Sensitive Detection of Picric acid.

    PubMed

    Pal, Ayan; Sk, Md Palashuddin; Chattopadhyay, Arun

    2016-03-01

    We report the conducting nature of carbon dots (Cdots) synthesized from citric acid and ethylene diamine. Chemically synthesized conducting nanocomposite consisting of Cdots and polypyrrole (PPy) is further reported, which showed higher electrical conductiviy in comparison to the components i.e., Cdots or PPy. The conductive film of the composite material was used for highly sensitive and selective detection of picric acid in water as well as in soil. To the best of our knowledge, this is the first report on the conductivity based sensing application of Cdot nanocomposite contrary to the traditional fluorescence based sensing approaches. PMID:26881300

  4. Carbon quantum dots with photo-generated proton property as efficient visible light controlled acid catalyst

    NASA Astrophysics Data System (ADS)

    Li, Haitao; Liu, Ruihua; Kong, Weiqian; Liu, Juan; Liu, Yang; Zhou, Lei; Zhang, Xing; Lee, Shuit-Tong; Kang, Zhenhui

    2013-12-01

    Developing light-driven acid catalyst will be very meaningful for the controlled-acid catalytic processes towards a green chemical industry. Here, based on scanning electrochemical microscopy (SECM) and ?pH testing, we demonstrate that the 5-10 nm carbon quantum dots (CQDs) synthesized by electrochemical ablation of graphite have strong light-induced proton properties under visible light in solution, which can be used as an acid catalyst. The 5-10 nm CQDs' catalytic activity is strongly dependent on the illumination intensity and the temperature of the reaction system. As an effective visible light driven and controlled acid-catalyst, 5-10 nm CQDs can catalyze a series of organic reactions (esterification, Beckmann rearrangement and aldol condensation) with high conversion (34.7-46.2%, respectively) in water solution under visible light, while the 1-4 nm CQDs and 10-2000 nm graphite do not have such excellent catalytic activity. The use of 5-10 nm CQDs as a light responsive and controllable photocatalyst is truly a novel application of carbon-based nanomaterials, which may significantly push research in the current catalytic industry, environmental pollution and energy issues.Developing light-driven acid catalyst will be very meaningful for the controlled-acid catalytic processes towards a green chemical industry. Here, based on scanning electrochemical microscopy (SECM) and ?pH testing, we demonstrate that the 5-10 nm carbon quantum dots (CQDs) synthesized by electrochemical ablation of graphite have strong light-induced proton properties under visible light in solution, which can be used as an acid catalyst. The 5-10 nm CQDs' catalytic activity is strongly dependent on the illumination intensity and the temperature of the reaction system. As an effective visible light driven and controlled acid-catalyst, 5-10 nm CQDs can catalyze a series of organic reactions (esterification, Beckmann rearrangement and aldol condensation) with high conversion (34.7-46.2%, respectively) in water solution under visible light, while the 1-4 nm CQDs and 10-2000 nm graphite do not have such excellent catalytic activity. The use of 5-10 nm CQDs as a light responsive and controllable photocatalyst is truly a novel application of carbon-based nanomaterials, which may significantly push research in the current catalytic industry, environmental pollution and energy issues. Electronic supplementary information (ESI) available. See DOI: 10.1039/c3nr03996j

  5. Scalable, non-invasive glucose sensor based on boronic acid functionalized carbon nanotube transistors

    NASA Astrophysics Data System (ADS)

    Lerner, Mitchell B.; Kybert, Nicholas; Mendoza, Ryan; Villechenon, Romain; Bonilla Lopez, Manuel A.; Charlie Johnson, A. T.

    2013-05-01

    We developed a scalable, label-free all-electronic sensor for D-glucose based on a carbon nanotube transistor functionalized with pyrene-1-boronic acid. This sensor responds to glucose in the range 1 ?M-100 mM, which includes typical glucose concentrations in human blood and saliva. Control experiments establish that functionalization with the boronic acid provides high sensitivity and selectivity for glucose. The devices show better sensitivity than commercial blood glucose meters and could represent a general strategy to bloodless glucose monitoring by detecting low concentrations of glucose in saliva.

  6. Emissions of organic aerosol mass, black carbon, particle number, and regulated and unregulated gases from scooters and light and heavy duty vehicles with different fuels

    NASA Astrophysics Data System (ADS)

    Chirico, R.; Clairotte, M.; Adam, T. W.; Giechaskiel, B.; Heringa, M. F.; Elsasser, M.; Martini, G.; Manfredi, U.; Streibel, T.; Sklorz, M.; Zimmermann, R.; DeCarlo, P. F.; Astorga, C.; Baltensperger, U.; Prevot, A. S. H.

    2014-06-01

    A sampling campaign with seven different types of vehicles was conducted in 2009 at the vehicle test facilities of the Joint Research Centre (JRC) in Ispra (Italy). The vehicles chosen were representative of some categories circulating in Europe and were fueled either with standard gasoline or diesel and some with blends of rapeseed methyl ester biodiesel. The aim of this work was to improve the knowledge about the emission factors of gas phase and particle-associated regulated and unregulated species from vehicle exhaust. Unregulated species such as black carbon (BC), primary organic aerosol (OA) content, particle number (PN), monocyclic and polycyclic aromatic hydrocarbons (PAHs) and a~selection of unregulated gaseous compounds, including nitrous acid (N2O), ammonia (NH3), hydrogen cyanide (HCN), formaldehyde (HCHO), acetaldehyde (CH3CHO), sulfur dioxide (SO2), and methane (CH4), were measured in real time with a suite of instruments including a high-resolution aerosol time-of-flight mass spectrometer, a resonance enhanced multi-photon ionization time-of-flight mass spectrometer, and a high resolution Fourier transform infrared spectrometer. Diesel vehicles, without particle filters, featured the highest values for particle number, followed by gasoline vehicles and scooters. The particles from diesel and gasoline vehicles were mostly made of BC with a low fraction of OA, while the particles from the scooters were mainly composed of OA. Scooters were characterized by super high emissions factors for OA, which were orders of magnitude higher than for the other vehicles. The heavy duty diesel vehicle (HDDV) featured the highest nitrogen oxides (NOx) emissions, while the scooters had the highest emissions for total hydrocarbons and aromatic compounds due to the unburned and partially burned gasoline and lubricant oil mixture. Generally, vehicles fuelled with biodiesel blends showed lower emission factors of OA and total aromatics than those from the standard fuels. The scooters were the main emitters of aromatic compounds, followed by the gasoline vehicle, the diesel vehicles and the HDDV.

  7. Separation of polar gases from nonpolar gases

    DOEpatents

    Kulprathipanja, Santi (Hoffman Estates, IL)

    1986-01-01

    The separation of polar gases from nonpolar gases may be effected by passing a mixture of nonpolar gases over the face of a multicomponent membrane at separation conditions. The multicomponent membrane which is used to effect the separation will comprise a mixture of a glycol plasticizer having a molecular weight of from about 200 to about 600 and an organic polymer cast on a porous support. The porous support is pretreated prior to casting of the mixture thereon by contact with a polyhydric alcohol whereby the pores of the support are altered, thus adding to the increased permeability of the polar gas.

  8. Separation of polar gases from nonpolar gases

    DOEpatents

    Kulprathipanja, S.

    1986-08-19

    The separation of polar gases from nonpolar gases may be effected by passing a mixture of nonpolar gases over the face of a multicomponent membrane at separation conditions. The multicomponent membrane which is used to effect the separation will comprise a mixture of a glycol plasticizer having a molecular weight of from about 200 to about 600 and an organic polymer cast on a porous support. The porous support is pretreated prior to casting of the mixture thereon by contact with a polyhydric alcohol whereby the pores of the support are altered, thus adding to the increased permeability of the polar gas.

  9. Carbon honeycomb grids for advanced lead-acid batteries. Part I: Proof of concept

    NASA Astrophysics Data System (ADS)

    Kirchev, Angel; Kircheva, Nina; Perrin, Marion

    2011-10-01

    The carbon honeycomb grid is proposed as innovative solution for high energy density lead acid battery. The proof of concept is demonstrated, developing grids suitable for the small capacity, scale of valve-regulated lead acid batteries with 2.5-3 Ah plates. The manufacturing of the grids, includes fast, known and simple processes which can be rescaled for mass production with a minimum, investment costs. The most critical process of green composite carbonisation by heating in inert, atmosphere from 200 to 1000 C takes about 5 h, guaranteeing the low cost of the grids. An AGM-VRLA, cell with prototype positive plate based on the lead-2% tin electroplated carbon honeycomb grid and, conventional negative plates is cycled demonstrating 191 deep cycles. The impedance spectroscopy, measurements indicate the grid performance remains acceptable despite the evolution of the corrosion, processes during the cycling.

  10. Modulation of Acetone-Butanol-Ethanol Fermentation by Carbon Monoxide and Organic Acids

    PubMed Central

    Datta, Rathin; Zeikus, J. G.

    1985-01-01

    Metabolic modulation of acetone-butanol-ethanol fermentation by Clostridium acetobutylicum with carbon monoxide (CO) and organic acids is described. CO, which is a known inhibitor of hydrogenase, was found to be effective in the concentration range of dissolved CO corresponding to a CO partial pressure of 0.1 to 0.2 atm. Metabolic modulation by CO was particularly effective when organic acids such as acetic and butyric acids were added to the fermentation as electron sinks. The uptake of organic acids was enhanced, and increases in butyric acid uptake by 50 to 200% over control were observed. Hydrogen production could be reduced by 50% and the ratio of solvents could be controlled by CO modulation and organic acid addition. Acetone production could be eliminated if desired. Butanol yield could be increased by 10 to 15%. Total solvent yield could be increased 1 to 3% and the electron efficiency to acetone-butanol-ethanol solvents could be increased from 73 to 78% for controls to 80 to 85% for CO- and organic acid-modulated fermentations. Based on these results, the dynamic nature of electron flow in this fermentation has been elucidated and mechanisms for metabolic control have been hypothesized. PMID:16346746

  11. In vitro inhibition of salicylic acid derivatives on human cytosolic carbonic anhydrase isozymes I and II.

    PubMed

    Bayram, Esra; Senturk, Murat; Kufrevioglu, O Irfan; Supuran, Claudiu T

    2008-10-15

    The inhibition of two human cytosolic carbonic anhydrase (hCA, EC 4.2.1.1) isozymes, hCA I and II, with a series of salicylic acid derivatives was investigated by using the esterase method with 4-nitrophenyl acetate as substrate. IC(50) values for sulfasalazine, diflunisal, 5-chlorosalicylic acid, dinitrosalicylic acid, 4-aminosalicylic acid, 4-sulfosalicylic acid, 5-sulfosalicylic acid, salicylic acid, acetylsalicylic acid (aspirin) and 3-metylsalicylic acid were of 3.04 microM, 3.38 microM, 4.07 microM, 7.64 microM, 0.13 mM, 0.29 mM, 0.42 mM, 0.56 mM, 2.71 mM and 3.07 mM for hCA I and of 4.49 microM, 2.70 microM, 0.72 microM, 2.80 microM, 0.75 mM, 0.72 mM, 0.29 mM, 0.68 mM, 1.16 mM and 4.70 mM for hCA II, respectively. Lineweaver-Burk plots were also used for the determination of the inhibition mechanism of these substituted phenols, most of which were noncompetitive inhibitors with this substrate. Some salicylic acid derivatives investigated here showed effective hCA I and II inhibitory activity, and might be used as leads for generating enzyme inhibitors eventually targeting other isoforms which have not been assayed yet for their interactions with such agents. PMID:18819808

  12. Influence of dissolved organic carbon content on modelling natural organic matter acid-base properties.

    PubMed

    Garnier, Cdric; Mounier, Stphane; Benam, Jean Yves

    2004-10-01

    Natural organic matter (NOM) behaviour towards proton is an important parameter to understand NOM fate in the environment. Moreover, it is necessary to determine NOM acid-base properties before investigating trace metals complexation by natural organic matter. This work focuses on the possibility to determine these acid-base properties by accurate and simple titrations, even at low organic matter concentrations. So, the experiments were conducted on concentrated and diluted solutions of extracted humic and fulvic acid from Laurentian River, on concentrated and diluted model solutions of well-known simple molecules (acetic and phenolic acids), and on natural samples from the Seine river (France) which are not pre-concentrated. Titration experiments were modelled by a 6 acidic-sites discrete model, except for the model solutions. The modelling software used, called PROSECE (Programme d'Optimisation et de SpEciation Chimique dans l'Environnement), has been developed in our laboratory, is based on the mass balance equilibrium resolution. The results obtained on extracted organic matter and model solutions point out a threshold value for a confident determination of the studied organic matter acid-base properties. They also show an aberrant decreasing carboxylic/phenolic ratio with increasing sample dilution. This shift is neither due to any conformational effect, since it is also observed on model solutions, nor to ionic strength variations which is controlled during all experiments. On the other hand, it could be the result of an electrode troubleshooting occurring at basic pH values, which effect is amplified at low total concentration of acidic sites. So, in our conditions, the limit for a correct modelling of NOM acid-base properties is defined as 0.04 meq of total analysed acidic sites concentration. As for the analysed natural samples, due to their high acidic sites content, it is possible to model their behaviour despite the low organic carbon concentration. PMID:15350419

  13. Isotopic composition of Murchison organic compounds: Intramolecular carbon isotope fractionation of acetic acid. Simulation studies of cosmochemical organic syntheses

    NASA Technical Reports Server (NTRS)

    Yuen, G. U.; Cronin, J. R.; Blair, N. E.; Desmarais, D. J.; Chang, S.

    1991-01-01

    Recently, in our laboratories, samples of Murchison acetic acid were decarboxylated successfully and the carbon isotopic composition was measured for the methane released by this procedure. These analyses showed significant differences in C-13/C-12 ratios for the methyl and carboxyl carbons of the acetic acid molecule, strongly suggesting that more than one carbon source may be involved in the synthesis of the Murchison organic compounds. On the basis of this finding, laboratory model systems simulating cosmochemical synthesis are being studied, especially those processes capable of involving two or more starting carbon sources.

  14. The erosion of carbonate stone by acid rain: Laboratory and field investigations

    USGS Publications Warehouse

    Baedecker, P.A.; Reddy, M.M.

    1993-01-01

    One of the goals of research on the effects of acidic deposition on carbonate stone surfaces is to define the incremental impact of acidic deposition relative to natural weathering processes on the rate of carbonate stone erosion. If rain that impacts carbonate stone surfaces is resident on the surface long enough to approach chemical equilibrium, the incremental effect of hydrogen ion is expected to be small (i.e., 6% for a rain of pH 4.0). Under nonequilibrium (i.e., high flow rate) conditions, kinetic considerations suggest that the incremental effect of hydrogen ion deposition could be quite significant. Field run-off experiments involving the chemical analysis of rain collected from inclined stone slabs have been used to evaluate stone dissolution processes under ambient conditions of wet and dry deposition of acidic species. The stoichiometry of the reaction of stone with hydrogen ion is difficult to define from the field data due to scatter in the data attributed to hydrodynamic effects. Laboratory run-off experiments show that the stoichiometry is best defined by a reaction with H+ in which CO2 is released from the system. The baseline effect caused by water in equilibrium with atmospheric CO2 is identical in the field and in laboratory simulation. The experiments show that the solutions are close enough to equilibrium for the incremental effect of hydrogen ion to be minor (i.e., 24% for marble for a rain of pH 4.0) relative to dissolution due to water and carbonic acid reactions. Stone erosion rates based on physical measurement are approximately double the recession rates that are due to dissolution (estimated from the observed calcium content of the run-off solutions). The difference may reflect the loss of granular material not included in recession estimates based on the run-off data. Neither the field nor the laboratory run-off experiments indicate a pH dependence for the grain-removal process.

  15. Salicylhydroxamic Acid (SHAM) Inhibition of the Dissolved Inorganic Carbon Concentrating Process in Unicellular Green Algae.

    PubMed

    Goyal, A; Tolbert, N E

    1990-03-01

    Rates of photosynthetic O(2) evolution, for measuring K(0.5)(CO(2) + HCO(3) (-)) at pH 7, upon addition of 50 micromolar HCO(3) (-) to air-adapted Chlamydomonas, Dunaliella, or Scenedesmus cells, were inhibited up to 90% by the addition of 1.5 to 4.0 millimolar salicylhydroxamic acid (SHAM) to the aqueous medium. The apparent K(1)(SHAM) for Chlamydomonas cells was about 2.5 millimolar, but due to low solubility in water effective concentrations would be lower. Salicylhydroxamic acid did not inhibit oxygen evolution or accumulation of bicarbonate by Scenedesmus cells between pH 8 to 11 or by isolated intact chloroplasts from Dunaliella. Thus, salicylhydroxamic acid appears to inhibit CO(2) uptake, whereas previous results indicate that vanadate inhibits bicarbonate uptake. These conclusions were confirmed by three test procedures with three air-adapted algae at pH 7. Salicylhydroxamic acid inhibited the cellular accumulation of dissolved inorganic carbon, the rate of photosynthetic O(2) evolution dependent on low levels of dissolved inorganic carbon (50 micromolar Na-HCO(3)), and the rate of (14)CO(2) fixation with 100 micromolar [(14)C] HCO(3) (-). Salicylhydroxamic acid inhibition of O(2) evolution and (14)CO(2)-fixation was reversed by higher levels of NaHCO(3). Thus, salicylhydroxamic acid inhibition was apparently not affecting steps of photosynthesis other than CO(2) accumulation. Although salicylhydroxamic acid is an inhibitor of alternative respiration in algae, it is not known whether the two processes are related. PMID:16667326

  16. Inertisation of galvanic sludge with calcium oxide, activated carbon, and phosphoric acid.

    PubMed

    Ore?anin, Vinja; Lovren?i? Mikeli?, Ivanka; Kollar, Robert; Mikuli?, Nenad; Meduni?, Gordana

    2012-09-01

    In this study we compared three methods for the treatment of electroplating sludge highly loaded with zinc and iron: (1) calcium oxide-based solidification/stabilisation; (2) conversion into inert material by adsorption of organic and inorganic pollutants onto activated carbon; and (3) conversion of mobile waste components into insoluble phosphates. All three methods proved highly efficient in the conversion of hazardous waste into inert material. Under optimum treatment conditions zinc concentration in the leachate of solidified waste was reduced by 99.7 % compared to untreated sludge. Zinc retention efficiency in the waste treated with activated carbon and phosphoric acid was 99.9 % and 98.7 %, respectively. The advantages of electroplating sludge treatment with activated carbon over the other two methods are high sorption capacity, insignificant pH and volume changes of the sludge, and simple use. PMID:23152383

  17. Free nitrous acid pretreatment of wasted activated sludge to exploit internal carbon source for enhanced denitrification.

    PubMed

    Ma, Bin; Peng, Yongzhen; Wei, Yan; Li, Baikun; Bao, Peng; Wang, Yayi

    2015-03-01

    Using internal carbon source contained in waste activated sludge (WAS) is beneficial for nitrogen removal from wastewater with low carbon/nitrogen ratio, but it is usually limited by sludge disintegration. This study presented a novel strategy based on free nitrous acid (FNA) pretreatment to intensify the release of organic matters from WAS for enhanced denitrification. During FNA pretreatment, soluble chemical oxygen demand (SCOD) production kept increasing when FNA increased from 0 to 2.04 mg HNO2-N/L. Compared with untreated WAS, the internal carbon source production increased by 50% in a simultaneous fermentation and denitrification reactor fed with WAS pretreated by FNA for 24 h at 2.04 mg HNO2-N/L. This also increased denitrification efficiency by 76% and sludge reduction by 87.5%. More importantly, greenhouse gas nitrous oxide production in denitrification was alleviated since more electrons could be provided by FNA pretreated WAS. PMID:25514398

  18. Biotechnological Production of Docosahexaenoic Acid Using Aurantiochytrium limacinum: Carbon Sources Comparison And Growth Characterization

    PubMed Central

    Abad, Sergi; Turon, Xavier

    2015-01-01

    Aurantiochytrium limacinum, a marine heterotrophic protist/microalga has shown interesting yields of docosahexaenoic acid (DHA) when cultured with different carbon sources: glucose, pure and crude glycerol. A complete study in a lab-scale fermenter allowed for the characterization and comparison of the growth kinetic parameters corresponding to each carbon source. Artificial Marine Medium (AMM) with glucose, pure and crude glycerol offered similar biomass yields. The net growth rates (0.10–0.12 h−1), biomass (0.7–0.8 g cells/g Substrate) and product (0.14–0.15 g DHA/g cells) yields, as well as DHA productivity were similar using the three carbon sources. Viable potential applications to valorize crude glycerol are envisioned to avoid an environmental problem due to the excess of byproduct. PMID:26690180

  19. Biotechnological Production of Docosahexaenoic Acid Using Aurantiochytrium limacinum: Carbon Sources Comparison And Growth Characterization.

    PubMed

    Abad, Sergi; Turon, Xavier

    2015-01-01

    Aurantiochytrium limacinum, a marine heterotrophic protist/microalga has shown interesting yields of docosahexaenoic acid (DHA) when cultured with different carbon sources: glucose, pure and crude glycerol. A complete study in a lab-scale fermenter allowed for the characterization and comparison of the growth kinetic parameters corresponding to each carbon source. Artificial Marine Medium (AMM) with glucose, pure and crude glycerol offered similar biomass yields. The net growth rates (0.10-0.12 h(-1)), biomass (0.7-0.8 g cells/g Substrate) and product (0.14-0.15 g DHA/g cells) yields, as well as DHA productivity were similar using the three carbon sources. Viable potential applications to valorize crude glycerol are envisioned to avoid an environmental problem due to the excess of byproduct. PMID:26690180

  20. Hyaluronic acid modified mesoporous carbon nanoparticles for targeted drug delivery to CD44-overexpressing cancer cells

    NASA Astrophysics Data System (ADS)

    Wan, Long; Jiao, Jian; Cui, Yu; Guo, Jingwen; Han, Ning; Di, Donghua; Chang, Di; Wang, Pu; Jiang, Tongying; Wang, Siling

    2016-04-01

    In this paper, hyaluronic acid (HA) functionalized uniform mesoporous carbon spheres (UMCS) were synthesized for targeted enzyme responsive drug delivery using a facile electrostatic attraction strategy. This HA modification ensured stable drug encapsulation in mesoporous carbon nanoparticles in an extracellular environment while increasing colloidal stability, biocompatibility, cell-targeting ability, and controlled cargo release. The cellular uptake experiments of fluorescently labeled mesoporous carbon nanoparticles, with or without HA functionalization, demonstrated that HA-UMCS are able to specifically target cancer cells overexpressing CD44 receptors. Moreover, the cargo loaded doxorubicin (DOX) and verapamil (VER) exhibited a dual pH and hyaluronidase-1 responsive release in the tumor microenvironment. In addition, VER/DOX/HA-UMCS exhibited a superior therapeutic effect on an in vivo HCT-116 tumor in BALB/c nude mice. In summary, it is expected that HA-UMCS will offer a new method for targeted co-delivery of drugs to tumors overexpressing CD44 receptors.

  1. Pseudo-capacitance on exfoliated carbon fiber in sulfuric acid electrolyte

    NASA Astrophysics Data System (ADS)

    Soneda, Y.; Yamashita, J.; Kodama, M.; Hatori, H.; Toyoda, M.; Inagaki, M.

    2006-03-01

    The specific capacitance of exfoliated carbon fibers (ExCF) which were synthesized from pitch-based carbon fibers showed a strong dependence with the concentration of sulfuric acid electrolyte and reached 1.4 F/m2 in 18 M H2SO4 solution. Since the capacitance value is quite large compared with the case of conventional activated carbons, faradic reactions (charge transfer reactions) are the cause of pseudo-capacitance. ExCF, however, gave a featureless cyclic voltammogram in 18 M H2SO4 solution. In the case of exfoliated natural graphite, the intercalation of H2SO4 molecules is evidenced by redox peaks observed in the voltammograms in the same conditions. Therefore, a strong interaction between the H2SO4 molecules and the ExCF surface might be the reason for the origin of pseudo-capacitance with ExCF in H2SO4 electrolyte.

  2. Tracing Carbon Sources through Aquatic and Terrestrial Food Webs Using Amino Acid Stable Isotope Fingerprinting

    PubMed Central

    Larsen, Thomas; Ventura, Marc; Andersen, Nils; OBrien, Diane M.; Piatkowski, Uwe; McCarthy, Matthew D.

    2013-01-01

    Tracing the origin of nutrients is a fundamental goal of food web research but methodological issues associated with current research techniques such as using stable isotope ratios of bulk tissue can lead to confounding results. We investigated whether naturally occurring ?13C patterns among amino acids (?13CAA) could distinguish between multiple aquatic and terrestrial primary production sources. We found that ?13CAA patterns in contrast to bulk ?13C values distinguished between carbon derived from algae, seagrass, terrestrial plants, bacteria and fungi. Furthermore, we showed for two aquatic producers that their ?13CAA patterns were largely unaffected by different environmental conditions despite substantial shifts in bulk ?13C values. The potential of assessing the major carbon sources at the base of the food web was demonstrated for freshwater, pelagic, and estuarine consumers; consumer ?13C patterns of essential amino acids largely matched those of the dominant primary producers in each system. Since amino acids make up about half of organismal carbon, source diagnostic isotope fingerprints can be used as a new complementary approach to overcome some of the limitations of variable source bulk isotope values commonly encountered in estuarine areas and other complex environments with mixed aquatic and terrestrial inputs. PMID:24069196

  3. N-doped carbon nanomaterials are durable catalysts for oxygen reduction reaction in acidic fuel cells.

    PubMed

    Shui, Jianglan; Wang, Min; Du, Feng; Dai, Liming

    2015-02-01

    The availability of low-cost, efficient, and durable catalysts for oxygen reduction reaction (ORR) is a prerequisite for commercialization of the fuel cell technology. Along with intensive research efforts of more than half a century in developing nonprecious metal catalysts (NPMCs) to replace the expensive and scarce platinum-based catalysts, a new class of carbon-based, low-cost, metal-free ORR catalysts was demonstrated to show superior ORR performance to commercial platinum catalysts, particularly in alkaline electrolytes. However, their large-scale practical application in more popular acidic polymer electrolyte membrane (PEM) fuel cells remained elusive because they are often found to be less effective in acidic electrolytes, and no attempt has been made for a single PEM cell test. We demonstrated that rationally designed, metal-free, nitrogen-doped carbon nanotubes and their graphene composites exhibited significantly better long-term operational stabilities and comparable gravimetric power densities with respect to the best NPMC in acidic PEM cells. This work represents a major breakthrough in removing the bottlenecks to translate low-cost, metal-free, carbon-based ORR catalysts to commercial reality, and opens avenues for clean energy generation from affordable and durable fuel cells. PMID:26601132

  4. Amino acid diagenesis, organic carbon and nitrogen mineralization in surface sediments from the inner Oslofjord, Norway

    SciTech Connect

    Haugen, J.E. ); Lichtentaler, R. )

    1991-06-01

    Total hydrolyzed amino acids (THAA), total organic carbon (TOC), and total nitrogen (TN) have been measured in an oxic and anoxic surface sediment from the inner Oslofjord. Downcore variations of these parameters are ascribed to both diagenesis and changes in organic matter supply, the latter being most important. These changes are most prominent in the anoxic sediment, which reflects the eutrophication history of the innermost part of the fjord. Downcore, THAA content decreased from 3.8 to 2.0 mg/g (salt-free dry weight) in the oxic sediment and from 22.3 to 3.8 mg/g in the anoxic sediment. Total amino acid nitrogen varied between 17 and 34% of total nitrogen in the oxic, and 25 and 54% in the anoxic, sediment. Organic carbon and organic nitrogen accumulation rates and depth integrated mineralization rates are about three times higher in the anoxic sediment than in the oxic sediment. Recycling of amino acids accounted for 4 to 12% of the total organic carbon and 13 to 40% of the total organic nitrogen regenerated in these sediments.

  5. N-doped carbon nanomaterials are durable catalysts for oxygen reduction reaction in acidic fuel cells

    PubMed Central

    Shui, Jianglan; Wang, Min; Du, Feng; Dai, Liming

    2015-01-01

    The availability of low-cost, efficient, and durable catalysts for oxygen reduction reaction (ORR) is a prerequisite for commercialization of the fuel cell technology. Along with intensive research efforts of more than half a century in developing nonprecious metal catalysts (NPMCs) to replace the expensive and scarce platinum-based catalysts, a new class of carbon-based, low-cost, metal-free ORR catalysts was demonstrated to show superior ORR performance to commercial platinum catalysts, particularly in alkaline electrolytes. However, their large-scale practical application in more popular acidic polymer electrolyte membrane (PEM) fuel cells remained elusive because they are often found to be less effective in acidic electrolytes, and no attempt has been made for a single PEM cell test. We demonstrated that rationally designed, metal-free, nitrogen-doped carbon nanotubes and their graphene composites exhibited significantly better long-term operational stabilities and comparable gravimetric power densities with respect to the best NPMC in acidic PEM cells. This work represents a major breakthrough in removing the bottlenecks to translate low-cost, metal-free, carbon-based ORR catalysts to commercial reality, and opens avenues for clean energy generation from affordable and durable fuel cells. PMID:26601132

  6. Activated carbon cleanup of the acid gas feed to Claus sulfur plants

    SciTech Connect

    Harruff, L.G.; Bushkuhl, S.J.

    1996-12-31

    This paper presents the details of a recently developed novel process using activated carbon to remove hydrocarbon contaminants from the acid gas feed to Claus sulfur recovery units. Heavy hydrocarbons, particularly benzene, toluene and xylene (BTX) have been linked to coke formation and catalyst deactivation in Claus converters. This deactivation results in reduced sulfur recovery and increased sulfur emissions from these plants. This effect is especially evident in split flow Claus plants which bypass some of the acid gas feed stream around the initial combustion step because of a low hydrogen sulfide concentration. This new clean-up process was proven to be capable of removing 95% of the BTX and other C{sub 6}{sup +} hydrocarbons from acid gas over a wide range of actual plant conditions. Following the adsorption step, the activated carbon was easily regenerated using low pressure steam. A post regeneration drying step using plant fuel gas also proved beneficial. This technology was extensively pilot tested in Saudi Aramco`s facilities in Saudi Arabia. Full scale commercial units are planned for two plants in the near future with the first coming on-line in 1997. The process described here represents the first application of activated carbon in this service, and a patent has been applied for. The paper will discuss the pilot plant results and the issues involved in scale-up to commercial size.

  7. Potentially bioavailable natural organic carbon and hydrolyzable amino acids in aquifer sediments

    USGS Publications Warehouse

    Thomas, Lashun K.; Widdowson, Mark A.; Novak, John T.; Chapelle, Francis H.; Benner, Ronald; Kaiser, Karl

    2012-01-01

    This study evaluated the relationship between concentrations of operationally defined potentially bioavailable organic -carbon (PBOC) and hydrolyzable amino acids (HAAs) in sediments collected from a diverse range of chloroethene--contaminated sites. Concentrations of PBOC and HAA were measured using aquifer sediment samples collected at six selected study sites. Average concentrations of total HAA and PBOC ranged from 1.96 ± 1.53 to 20.1 ± 25.6 mg/kg and 4.72 ± 0.72 to 443 ± 65.4 mg/kg, respectively. Results demonstrated a statistically significant positive relationship between concentrations of PBOC and total HAA present in the aquifer sediment (p < 0.05). Higher levels of HAA were consistently observed at sites with greater levels of PBOC and first-order decay rates. Because amino acids are known to be readily biodegradable carbon compounds, this relationship suggests that the sequential chemical extraction procedure used to measure PBOC is a useful indicator of bioavailable carbon in aquifer sediments. This, in turn, is consistent with the interpretation that PBOC measurements can be used for estimating the amount of natural organic carbon available for driving the reductive dechlorination of chloroethenes in groundwater systems.

  8. Preliminary study on preparation of BCNO phosphor particles using citric acid as carbon source

    SciTech Connect

    Nuryadin, Bebeh W.; Pratiwi, Tripuspita; Faryuni, Irfana D.; Iskandar, Ferry Abdullah, Mikrajuddin; Khairurrijal; Ogi, Takashi; Okuyama, Kikuo

    2015-04-16

    A citric acid was used as a carbon source in the preparation of boron carbon oxy-nitride (BCNO) phosphor particles by a facile process. The preparation process was conducted at relatively low temperature 750 °C and at ambient pressure. The prepared BCNO phosphors showed a high photoluminescence (PL) performance at peak emission wavelength of 470 nm under excitation by a UV light 365 nm. The effects of carbon/boron and nitrogen/boron molar ratios on the PL properties were also investigated. The result showed that the emission spectra with a wavelength peak ranging from 444 nm to 496 nm can be obtained by varying carbon/boron ratios from 0.1 to 0.9. In addition, the observations showed that the BCNO phosphor material has two excitation peaks located at the 365 nm (UV) and 420 nm (blue). Based on these observations, we believe that the citric acid derived BCNO phosphor particles can be a promising inexpensive material for phosphor conversion-based white LED.

  9. Production of activated carbon from a new precursor molasses by activation with sulphuric acid.

    PubMed

    Legrouri, K; Khouya, E; Ezzine, M; Hannache, H; Denoyel, R; Pallier, R; Naslain, R

    2005-02-14

    Activated carbon has been prepared from molasses, a natural precursor of vegetable origin resulting from the sugar industry in Morocco. The preparation of the activated carbon from the molasses has been carried out by impregnation of the precursor with sulphuric acid, followed by carbonisation at varying conditions (temperature and gas coverage) in order to optimize preparation parameters. The influence of activation conditions was investigated by determination of adsorption capacity of methylene blue and iodine, the BET surface area, and the pore volume of the activated carbon were determined while the micropore volume was determined by the Dubinin-Radushkevich (DR) equation. The activated materials are mainly microporous and reveal the type I isotherm of the Brunauer classification for nitrogen adsorption. The activated carbons properties in this study were found for activation of the mixture (molasses/sulphuric acid) in steam at 750 degrees C. The samples obtained in this condition were highly microporous, with high surface area (> or =1200 m2/g) and the maximum adsorption capacity of methylene blue and iodine were 435 and 1430 mg/g, respectively. PMID:15721553

  10. Green House Gases Measurement At Maitri, Antarctica

    NASA Astrophysics Data System (ADS)

    Jain, S. L.; Ghude, S. D.; Arya, B. C.

    The earth's environment is constantly changing. The scientific evidence indicates that these changes are result of a complex interplay among a number of natural and human related systems. Therefore in the recent times, concern has grown about global change - which is related to natural and anthropogenic alteration of the Earth's environment. Among them the important issues, which are dangerous for the survival of life on the earth, are global green house warming, urban and regional atmospheric pollution, regional increases in tropospheric ozone, the decrease in stratospheric ozone in general and ozone hole over Antarctica in particular, acid rain etc. The monitoring of green house gases has an important role in the understanding of global change. The green house effect of CO_2 increase which has been the subject of scientific studies since later half of the nineteenth century but the CO_2 problem gained tremendous momentum during last two decades. Now it has been recognized that the green house effect due to trace gases such as CFC's, CH_4, O_3, N_2O, H_2O etc. is as much as that due to CO_2 while it was only due to CO_2 during pre industrial era to 1950's. In view of the above various state of art systems have been set up at Maitri, Antarctica for measurements of various green house gases, column ozone, water vapour, UV-B radiation, aerosol optical depth and vertical profiles of ozone which in turn will go a long way to fill in the gaps and provide valuable data for modeling studies. An automated gas chromatograph based experiment was setup in January 2002 at Maitri, for the measurements of green house gases, such as Carbon Dioxide (CO_2), Methane (CH_4) etc. The average concentration of CO_2 during the year 2002 is found out to be 367.42 ppm and average concentration of CH_4 from February to May 2003 is found out to be 1.69 ppm. An increase of about 1.6 ppm of CO_2 concentration was observed during the year 2002. The hourly mean mixing ratios of CO was found in the range 30 ppb to 65 ppb. Diurnal variation in CO concentrations was systematically observed with higher CO concentration in day time sunlit period. In the present communication the salient features of the highly sophisticated system such as laser heterodyne, sun photometer, gas chromatogram, CO analyzer setup for atmospheric studies at Maitri and the results obtained will be discussed in detail.

  11. Neutralizing Carbonic Acid in Deep Carbonate Strata below the North Atlantic

    SciTech Connect

    Klaus Lackner; Charles Harvey; Bruce Watson

    2008-01-14

    Carbon dioxide injection into deep sea sediments below 2700 m water depth and a few hundred meters to fifteen hundred meters deep in the sediment column may provide permanent geologic storage by gravitational trapping. At high pressures and low temperatures common in deep sea sediments a few hundred meters below sea floor, CO{sub 2} will be in its liquid phase and will be denser than the overlying pore fluid. The lower density of the pore fluid provides a cap to the denser CO{sub 2} and ensures gravitational trapping in the short term. The overall storage capacity for CO{sub 2} in such deep sea formations below the ocean floor is primarily determined by the permeability, and will vary with seafloor depth, geothermal gradient, porosity, and pore water salinity. Furthermore, the dissemination of the injected CO{sub 2} in the sediments and potential chemical reactions between CO{sub 2}, pore fluid and sediments will define its fate in the storage reservoir. The main objectives of our research was to evaluate the potential for sub-seabed CO{sub 2} storage in deep sea sediments using a range of approaches including experiments, permeability analysis, and modeling. Over the course of the three-year award, our results support an important role for sub-seabed storage in a diverse portfolio of carbons sequestration options. Our analysis has shown the feasibility of this type of storage, and also emphasizes that escape or leakage from such sites would be negligible. The most difficult challenge is to overcome the low permeability of typical deep-sea sediments, and a variety of approaches are suggested for future research.

  12. Hepatoprotective effect of Matrine salvianolic acid B salt on Carbon Tetrachloride-Induced Hepatic Fibrosis.

    PubMed

    Gao, Hong-Ying; Li, Guo-Yu; Lou, Meng-Meng; Li, Xiao-Yu; Wei, Xiu-Yan; Wang, Jin-Hui

    2012-01-01

    The aim of this study was to investigate the hepatoprotective effect of Matrine salvianolic acid B salt on carbon tetrachloride (CCl4)-induced hepatic fibrosis in rats. Salvianolic acid B and Matrine has long been used to treat liver fibrosis. Matrine salvianolic acid B salt is a new compound containing Salvianolic acid B and Matrine. Hepatic fibrosis induced by CCl4 was studied in animal models using Wistar rats. Organ coefficient, serum aspartate aminotransferase (AST), alanine aminotransferase (ALT), hexadecenoic acid (HA), laminin (LN), hydroxyproline (Hyp), and glutathione (GSH), malondialdehyde (MDA), superoxide dismutase (SOD) in liver tissues were measured, respectively. Histopathological changes in the livers were studied by hematoxylin-eosin (H&E) staining and Masson Trichrome (MT) examination. The expression of transforming growth factor-β1 (TGF-β1) and α-smooth muscle actin (α-SMA) was observed by immunohistochemical analysis. A significant reduction in serum levels of AST, ALT, HA, LN and Hyp was observed in the Matrine salvianolic acid B salt treated groups, suggesting that the salt had hepatoprotective effects. The depletion of GSH and SOD, as well as MDA accumulation in liver tissues was suppressed by Matrine salvianolic acid B salt too. The expression of TGF-β1 and α-SMA measured by immunohistology was significantly reduced by Matrine salvianolic acid B salt in a dose-dependent manner. Matrine salvianolic acid B salt treatment attenuated the necro-inflammation and fibrogenesis induced by CCl4 injection, and thus it is promising as a therapeutic anti-fibrotic agent against hepatic fibrosis. PMID:22559721

  13. An evaluation of waste gypsum-based precipitated calcium carbonate for acid mine drainage neutralization.

    PubMed

    Zvimba, J N; Mulopo, J; Bologo, L T; Mathye, M

    2012-01-01

    Precipitated CaCO(3) compounds recovered from pulped waste gypsum using some carbonate and hydroxide-based reagents were evaluated for their utilization in acid mine drainage (AMD) neutralization. The neutralization potentials, acid neutralization capacities and compositions of the CaCO(3) compounds were determined and compared with some commercial CaCO(3). It was observed that CaCO(3) recovered from waste gypsum using Na(2)CO(3) significantly neutralized AMD compared with commercial CaCO(3) and that recovered using both (NH(4))(2)CO(3) or NH(4)OH-CO(2) reagents. Moreover, a higher acid neutralization capacity of 1,370 kg H(2)SO(4)/t was determined for CaCO(3) recovered from waste gypsum using Na(2)CO(3) compared with an average of 721 and 1,081 kg H(2)SO(4)/t for ammonium-based CaCO(3) and commercial CaCO(3) respectively. The inorganic carbon content for the CaCO(3) recovered using Na(2)CO(3) and ammonium-based reagents of 49 and 34% respectively confirmed their observed neutralization potentials and acid neutralization capacities, while energy dispersive X-ray fluorescence suggested absence of major oxide impurities, with the exception of residual SO(4)(2-) and Na(2)O which still requires further reduction in the respective compounds. PMID:22508119

  14. Hydrogen Generation During the Corrosion of Carbon Steel in Oxalic Acid

    SciTech Connect

    WIERSMA, BRUCEJ.

    2004-08-01

    A literature review of the corrosion mechanism for carbon steel in oxalic acid was performed to determine the ratio of moles of iron corroded to moles of hydrogen evolved during the corrosion of iron in oxalic acid. The theory of corrosion of carbon steel in oxalic acid and experimental work were reviewed. It was concluded that the maximum ratio of moles of hydrogen evolved to moles of iron corroded is 1:1. This ratio would be observed in a de-aerated environment. If oxygen or other oxidizing species are present, the ratio could be much less than 1:1. Testing would be necessary to determine how much less than 1:1 the ratio might be. Although the ratio of hydrogen evolution to iron corroded will not exceed 1:1, the total amount of hydrogen evolved can be influenced by such things as a decrease in the exposed surface area, suppression of hydrogen generation by gamma radiation, the presence of corrosion products on steel surface, etc. These and other variables present during chemical cleaning operations of the waste tank have not been examined by the tests reported in the literature i.e., the tests have focused on clean corrosion coupons in oxalic acid solutions. It is expected that most of these variables would reduce the total amount of hydrogen evolved. Further testing would need to be performed to quantify the reduction in hydrogen generation rate associated with these variables.

  15. Improvement in electrochemical capacitance of activated carbon from scrap tires by nitric acid treatment

    NASA Astrophysics Data System (ADS)

    Han, Yan; Zhao, Ping-Ping; Dong, Xiao-Ting; Zhang, Cui; Liu, Shuang-Xi

    2014-12-01

    Activated carbon (AC) obtained from the industrial pyrolytic tire char is treated by concentrated nitric acid (AC-HNO3) and then used as the electrode material for supercapacitors. Surface properties and electrochemical capacitances of AC and ACHNO3 are studied. It is found that the morphology and the porous texture for AC and AC-HNO3 have little difference, while the oxygen content increases and functional groups change after the acid treatment. Electrochemical results demonstrate that the AC-HNO3 electrode displays higher specific capacitance, better stability and cycling performance, and lower equivalent series resistance, indicating that AC obtained from the industrial pyrolytic tire char treated by concentrated nitric acid is applicable for supercapacitors.

  16. Adsorption and properties of aromatic amino acids on single-walled carbon nanotubes

    NASA Astrophysics Data System (ADS)

    Wang, Cuihong; Li, Shuang; Zhang, Ruiqin; Lin, Zijing

    2012-02-01

    We investigated the adsorption of three aromatic amino acids--phenylalanine, tyrosine, and tryptophan--on the sidewalls of a number of representative single-walled carbon nanotubes (SWNTs) using density-functional tight-binding calculations, complemented by an empirical dispersion correction. The armchair (n, n) SWNTs (n = 3-12) and zigzag (n, 0) SWNTs (n = 4-12) were thoroughly examined. We found that the most stable amino acid/SWNT complexes for different SWNTs have similar local structures, and that the distance between the amino acid and SWNT is about 3 . Owing to the ?-? and H-? stacking interactions, the benzene and indole rings are not exactly parallel to the SWNTs but instead lie at a small angle. We also investigated the diameter and chirality dependences of binding energies and found that SWNT (5, 0) has an especially large binding energy that can be used for SWNT identification or selection.

  17. 40 CFR 52.22 - Enforceable commitments for further actions addressing the pollutant greenhouse gases (GHGs).

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ... actions addressing the pollutant greenhouse gases (GHGs). 52.22 Section 52.22 Protection of Environment... greenhouse gases (GHGs). (a) Definitions. (1) Greenhouse Gases (GHGs) means the air pollutant as defined in 86.1818-12(a) of this chapter as the aggregate group of six greenhouse gases: Carbon dioxide,...

  18. 40 CFR 52.22 - Enforceable commitments for further actions addressing the pollutant greenhouse gases (GHGs).

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ... actions addressing the pollutant greenhouse gases (GHGs). 52.22 Section 52.22 Protection of Environment... greenhouse gases (GHGs). (a) Definitions. (1) Greenhouse Gases (GHGs) means the air pollutant as defined in 86.1818-12(a) of this chapter as the aggregate group of six greenhouse gases: Carbon dioxide,...

  19. 40 CFR 52.22 - Enforceable commitments for further actions addressing the pollutant greenhouse gases (GHGs).

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ... actions addressing the pollutant greenhouse gases (GHGs). 52.22 Section 52.22 Protection of Environment... greenhouse gases (GHGs). (a) Definitions. (1) Greenhouse Gases (GHGs) means the air pollutant as defined in 86.1818-12(a) of this chapter as the aggregate group of six greenhouse gases: Carbon dioxide,...

  20. 40 CFR 52.22 - Enforceable commitments for further actions addressing the pollutant greenhouse gases (GHGs).

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... actions addressing the pollutant greenhouse gases (GHGs). 52.22 Section 52.22 Protection of Environment... greenhouse gases (GHGs). (a) Definitions. (1) Greenhouse Gases (GHGs) means the air pollutant as defined in § 86.1818-12(a) of this chapter as the aggregate group of six greenhouse gases: Carbon dioxide,...