WorldWideScience

Sample records for carbon 14 compounds

  1. Differential monitoring of tritium and carbon-14 compounds

    International Nuclear Information System (INIS)

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

  2. Carbon-14 waste management

    International Nuclear Information System (INIS)

    Carbon-14 occurs in nature, but is also formed in nuclear reactors. Because of its long half-life and the biological significance of carbon, releases from nuclear facilities could have a significant radiological impact. Waste management strategies for carbon-14 are therefore of current concern. Carbon-14 is present in a variety of waste streams both at reactors and at reprocessing plants. A reliable picture of the production and release of carbon-14 from various reactor systems has been built up for the purposes of this study. A possible management strategy for carbon-14 might be the reduction of nitrogen impurity levels in core materials, since the activation of 14N is usually the dominant source of carbon-14. The key problem in carbon-14 management is its retention of off-gas streams, particularly in the dissolver off-gas stream at reprocessing plants. Three alternative trapping processes that convert carbon dioxide into insoluble carbonates have been suggested. The results show that none of the options considered need be rejected on the grounds of potential radiation doses to individuals. All exposures should be as low as reasonably achievable, economic and social factors being taken into account. If, on these grounds, retention and disposal of carbon-14 is found to be beneficial, then, subject to the limitations noted, appropriate retention, immobilization and disposal technologies have been identified

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

    International Nuclear Information System (INIS)

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

  4. Compilation of carbon-14 data

    Energy Technology Data Exchange (ETDEWEB)

    Paasch, R.A.

    1985-07-08

    A review and critical analysis was made of the original sources of carbon-14 in the graphite moderator and reflector zones of the eight Hanford production reactors, the present physical and chemical state of the carbon-14, pathways (other than direct combustion) by which the carbon-14 could be released to the biosphere, and the maximum rate at which it might be released under circumstances which idealistically favor the release. Areas of uncertainty are noted and recommendations are made for obtaining additional data in three areas: (1) release rate of carbon-14 from irradiated graphite saturated with aerated water; (2) characterization of carbon-14 deposited outside the moderator and reflector zones; and (3) corrosion/release rate of carbon-14 from irradiated steel and aluminum alloys.

  5. Compilation of carbon-14 data

    International Nuclear Information System (INIS)

    A review and critical analysis was made of the original sources of carbon-14 in the graphite moderator and reflector zones of the eight Hanford production reactors, the present physical and chemical state of the carbon-14, pathways (other than direct combustion) by which the carbon-14 could be released to the biosphere, and the maximum rate at which it might be released under circumstances which idealistically favor the release. Areas of uncertainty are noted and recommendations are made for obtaining additional data in three areas: (1) release rate of carbon-14 from irradiated graphite saturated with aerated water; (2) characterization of carbon-14 deposited outside the moderator and reflector zones; and (3) corrosion/release rate of carbon-14 from irradiated steel and aluminum alloys

  6. Carbon 14 dating; La datation par le carbone 14

    Energy Technology Data Exchange (ETDEWEB)

    Laj, C.; Mazaud, A.; Duplessy, J.C. [CEA Saclay, Lab. des Sciences du Climat et de l' Environnement, 91 - Gif-sur-Yvette (France)

    2004-03-01

    In this article time dating based on carbon 14 method is reviewed, its limits are explained and recent improvements are presented. Carbon 14 is a by-product of the interactions of cosmic protons with air molecules. The fluctuations of the quantity of carbon 14 present in the atmosphere are responsible for the shift observed between the result given by the method and the real age. This shift appears for ages greater than 2000 years and is estimated to 1000 years for an age of 10.000 years. As a consequence carbon 14 dating method requires calibration by comparing with other methods like dendrochronology (till 11.000 years) and time dating of fossil corals (till 26.000 years and soon till 50.000 years). It is assumed that the fluctuations of carbon 14 in the atmosphere are due to: - the changes in the intensity and composition of cosmic radiations itself (due to the motion of the sun system through the galaxy or due to the explosion of a super-novae in the surroundings of the sun system); - the changes of the earth magnetic field that diverts cosmic rays; and - the changes in the interactions between the atmosphere and the oceans knowing that 40 tons of carbon 14 are dissolved in seas while only 1 ton belongs to the atmosphere. (A.C.)

  7. Carbon 14 dating method

    International Nuclear Information System (INIS)

    This document gives a first introduction to 14C dating as it is put into practice at the radiocarbon dating centre of Claude-Bernard university (Lyon-1 univ., Villeurbanne, France): general considerations and recalls of nuclear physics; the 14C dating method; the initial standard activity; the isotopic fractioning; the measurement of samples activity; the liquid-scintillation counters; the calibration and correction of 14C dates; the preparation of samples; the benzene synthesis; the current applications of the method. (J.S.)

  8. Elastic Scattering of CARBON-14 + CARBON-12, Carbon -14 + OXYGEN-16, and CARBON-14 + OXYGEN-18.

    Science.gov (United States)

    Sterbenz, Stephen Michael

    We have carried out highly detailed studies of the elastic scattering of ^{14} C from ^{12}C, ^{16}O, and ^ {18}O, in a search for resonant phenomena in heavy-ion systems of non-zero isospin and zero spin. Angular distributions from ^{14}C+ ^{12}C and ^ {14}C+^{16}O scattering were measured at ^{14} C bombarding energies ranging from 20 to 40.3 MeV in 0.35 MeV steps. ^{14}C+ ^{18}O angular distributions were measured at ^{14}C energies from 20 to 30 MeV in 0.40 MeV steps and from 22.5 to 32.5 MeV in 2.5 MeV steps. The great variety of behavior which characterizes heavy-ion scattering is clearly illustrated by our data. The ^{14}C+^ {12}C and ^{14} C+^{16}O systems both exhibit marked gross structure in their excitation functions and deep oscillatory structure with a large backward angle rise in their angular distributions. They are in sharp contrast with the ^{14} C+^{18}O system, where structure is not apparent, and cross-sections fall steeply at larger angles and higher energies. However, only in the ^{14}C+ ^{12}C system are the excitation functions strongly fragmented by intermediate width structure. The anomalous appearance of the ^{14} C+^{12}C angular distributions near 17.5 MeV (cm) does suggest the existence of a resonant state (tentatively identified as l = 10 by phase shift analysis). In our analysis, we point out that the remarkable qualitative differences among these systems may be related to open-channel systematics. We find that general characteristics of the ^{14}C+ ^{18}O data are reproduced with a strongly absorbing optical potential model, contrary to the situation in the other two systems, where a specific mechanism, such as elastic transfer, must be invoked to account for the backward rise. We have pursued analysis with a one-step DWBA elastic transfer model which was quite successful at low energies. Its underprediction of the backward rise at higher energies provides further evidence of the importance of multi-step processes in two

  9. Soil metabolic transformations of carbon-14-myo-inositol, carbon-14-phytic acid and carbon-14-iron(III) phytate

    International Nuclear Information System (INIS)

    Uniformly labelled 14C-phytic acid and 14C-iron(III) phytate were synthesized from uniformly labelled 14C-myo-inositol. The three compounds were incubated in an Andosol sandy loam at 70% field capacity and 36.50C for a 12-day period. Myo-inositol, phytic acid and iron(III) phytate underwent a 61.0, 1.9 and 0% microbial oxidation respectively to CO2 during the incubation period. The rate of fixation of 14C-phytic acid was illustrated by its rapid decline in metabolism in the 12-day period. The metabolism rate of phytic was considerably reduced by the presumed formation of iron(III) and aluminium phytate. The metabolism rate of myo-inositol was reduced nine-fold after an initial rapid metabolism during the first day of incubation. The following mechanisms were observed in the soil metabolism of myo-inositol: (1) soil mineral-inositol carbon adsorption, (2) humic acid-inositol carbon adsorption, (3) the phosphorylation of myo-inositol, and (4) the epimerization of myo-inositol to chiro-inositol. The formation of (1) and (2) was found to be highly dependent upon microbial activity. Interactions (1), (2) and (3)are considered as possible mechanisms for the inhibition of the microbial oxidation of myo-inositol. The inhibition of myo-inositol oxidation via adsorption or phosphorylation is considered to be due to the chemical blockage of the stereo-specific microbial oxidative attack on the axial hydroxyl group. (author)

  10. Biomass carbon-14 ratio measured by accelerator mass spectrometry

    International Nuclear Information System (INIS)

    Measurement methods of a biomass carbon ratio in biomass products based on 14C-radiocarbon concentration have been reviewed. Determination of the biomass carbon ratio in biomass products is important to secure the reliance in the commercial market, because the 'biomass products' could contain products from petroleum. The biomass carbon ratio can be determined from percent Modern Carbon (pMC) using ASTM D6866 methods. The pMC value is calculated from the comparison between the 14C in sample and 14C in reference material. The 14C concentration in chemical products can be measured by liquid scintillation counter (LSC) and accelerator mass spectrometry (AMS). LSC can be applicable to determine the biomass carbon ratio for liquid samples such as gasoline with bioethanol (E5 or E10). On the other hand, AMS can be used to determine the biomass carbon ratio for almost all kinds of organic and inorganic compounds such as starch, cellulose, ethanol, gasoline, or polymer composite with inorganic fillers. AMS can accept the gaseous and solid samples. The graphite derived from samples included in solid phase is measured by AMS. The biomass carbon of samples derived from wood were higher than 100% due to the effect of atomic bomb test in the atmosphere around 1950 which caused the artificial 14C injection. Exact calculation methods of the biomass carbon ratio from pMC will be required for the international standard (ISO standard). (author)

  11. Carbon-14 Bomb-Pulse Dating

    Energy Technology Data Exchange (ETDEWEB)

    Buchholz, B A

    2007-12-16

    Atmospheric testing of nuclear weapons during the 1950s and early 1960s doubled the concentration of carbon-14 atmosphere and created a pulse that labeled everything alive in the past 50 years as carbon moved up the food chain. The variation in carbon-14 concentration in time is well-documented and can be used to chronologically date all biological materials since the mid-1950s.

  12. The carbon 14 and environment; Le carbone 14 et l'environnement

    Energy Technology Data Exchange (ETDEWEB)

    NONE

    2007-07-01

    This article resume the history and the properties of the carbon 14 ({sup 14}C). We also find the different origins and the produced quantities. The carbon transfers in environment are explained and so the {sup 14}C. The biological effects and the sanitary aspects are clarified. The measurements of carbon 14 are given as well its application through the dating. The waste management is tackled. (N.C.)

  13. Heterocyclic compounds as carbonic anhydrase inhibitor.

    Science.gov (United States)

    Husain, Asif; Madhesia, Diwakar

    2012-12-01

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

  14. Analysis of lunar samples for carbon compounds.

    Science.gov (United States)

    Kvenvolden, K. A.

    1971-01-01

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

  15. Carbon compounds in the atmosphere and their chemical reactions

    OpenAIRE

    Martišová, Petra

    2013-01-01

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

  16. Evaluation of carbon-14 life cycle in reactors VVER-1000

    International Nuclear Information System (INIS)

    This work is aimed at the evaluation of carbon-14 life cycle in light water reactors VVER-1000. Carbon-14 is generated as a side product in different systems of nuclear reactors and has been an issue not only in radioactive waste management but mainly in release into the environment in the form of gaseous effluents. The principal sources of this radionuclide are in primary cooling water and fuel. Considerable amount of C-14 is generated by neutron reactions with oxygen 17O and nitrogen 14N present in water coolant and fuel. The reaction likelihood and consequently volume of generated radioisotope depends on several factors, especially on the effective cross-section, concentrations of parent elements and conditions of power plant operating strategies. Due to its long half-life and high capability of integration into the environment and thus into the living species, it is very important to monitor the movement of carbon-14 in all systems of nuclear power plant and to manage its release out of NPP. The dominant forms of radioactive carbon-14 are the hydrocarbons owing to the combinations with hydrogen used for absorption of radiolytic oxygen. These organic compounds, such as formaldehyde, methyl alcohol, ethyl alcohol and formic acid can be mostly retained on ion exchange resins used in the system for purifying primary cooling water. The gaseous carbon compounds (CH4 and CO2) are released into the atmosphere via the ventilation systems of NPP. Based on the information and data obtained from different sources, it has been designed a balance model of possible carbon-14 pathways throughout the whole NPP. This model includes also mass balance model equations for each important node in system and available sampling points which will be the background for further calculations. This document is specifically not to intended to describe the best monitoring program attributes or technologies but rather to provide evaluation of obtained data and find the optimal way to upgrade

  17. Synthesis of carbon-14 labeled doxylamine succinate

    International Nuclear Information System (INIS)

    Doxylamine succinate, N,N-dimethyl-2-[1-phenyl-1-(2-pyridinyl)-ethoxy]ethanamine succinate is an antihistamine used primarily as a sedative. Carbon-14 labeled doxylamine succinate, required for toxicological studies, was synthesized in two steps starting from 2-benzoyl pyridine. (author)

  18. Laser ablation of molecular carbon nitride compounds

    Energy Technology Data Exchange (ETDEWEB)

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

    2015-09-15

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

  19. Carbon-Based Compounds and Exobiology

    Science.gov (United States)

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

    1996-01-01

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

  20. Removal of carbon-14 from irradiated graphite

    Science.gov (United States)

    Dunzik-Gougar, Mary Lou; Smith, Tara E.

    2014-08-01

    Approximately 250,000 tonnes of irradiated graphite waste exists worldwide and that quantity is expected to increase with decommissioning of Generation II reactors and deployment of Generation IV gas-cooled, graphite moderated reactors. This situation indicates the need for a graphite waste management strategy. On of the isotopes of great concern for long-term disposal of irradiated graphite is carbon-14 (14C), with a half-life of 5730 years. Study of irradiated graphite from some nuclear reactors indicates 14C is concentrated on the outer 5 mm of the graphite structure. The aim of the research presented here is to develop a practical method by which 14C can be removed. In parallel with these efforts, the same irradiated graphite material is being characterized to identify the chemical form of 14C in irradiated graphite. A nuclear-grade graphite, NBG-18, and a high-surface-area graphite foam, POCOFoam®, were exposed to liquid nitrogen (to increase the quantity of 14C precursor) and neutron-irradiated (1013 neutrons/cm2/s). During post-irradiation thermal treatment, graphite samples were heated in the presence of an inert carrier gas (with or without the addition of an oxidant gas), which carries off gaseous products released during treatment. Graphite gasification occurs via interaction with adsorbed oxygen complexes. Experiments in argon only were performed at 900 °C and 1400 °C to evaluate the selective removal of 14C. Thermal treatment also was performed with the addition of 3 and 5 vol% oxygen at temperatures 700 °C and 1400 °C. Thermal treatment experiments were evaluated for the effective selective removal of 14C. Lower temperatures and oxygen levels correlated to more efficient 14C removal.

  1. A gaseous measurement system for carbon-14 dioxide and carbon-14 methane: An analytical methodology to be applied in the evaluation of the carbon-14 dioxide and carbon-14 methane produced via microbial activity in volcanic tuff

    International Nuclear Information System (INIS)

    The objectives of this study were to develop a gaseous measurement system for the carbon-14 dioxide and carbon-14 methane produced via microbial activity or geochemical action on leachate in tuff; to determine the trapping efficiency of the system for carbon-14 dioxide; to determine the trapping efficiency of the system for carbon-14 methane; to apply the experimentally determined factors regarding the system's trapping efficiency for carbon-14 dioxide and carbon-14 methane to a trapping algorithm to determine the activity of the carbon-14 dioxide and carbon-14 methane in a mixed sample; to determine the minimum detectable activity of the measurement process in picocuries per liter; and to determine the lower limit or detection of the measurement process in counts per minute

  2. LDEO Carbon 14 Data from Selected Sea floor Cores

    Data.gov (United States)

    National Oceanic and Atmospheric Administration, Department of Commerce — Carbon-14 data in this file were compiled by W.F. Ruddiman and staff at the Lamont-Doherty Earth Observatory of Columbia University. Data include 974 carbon-14...

  3. The bonds in the cluster compound CZr6I14

    International Nuclear Information System (INIS)

    The electronic properties of the cluster compound CZr6I14 are discussed on the basis of EHT results. In the model cluster CZr6I184-the calculated Zr-Zr distance in the metal octahedron is enlarged by encapsulation of the interstitial C as well as by the surrounding ligands. The interstitial bond is realized by the two bond orbitals a1g, t1u, and, additionally, by three t1u orbitals of the 5 p(I) band. The Zr-Zr bonds are week. The cluster CZr6T184- is held together by strong C-Zr and Zr-I bonds. (author)

  4. The lichens, tritium and carbon 14 integrators; Les lichens, integrateurs de tritium et de carbone 14

    Energy Technology Data Exchange (ETDEWEB)

    Daillant, O

    2007-07-01

    The present report concerns a research for the tritium and for the carbon 14 in lichens in a spirit of bio-indication: the first results appear in Daillant and al (2004 ) and additional results were presented to the congress B.I.O.M.A.P. in Slovenia, organized collectively by the institute Josef Stefan from Ljubljana and the international atomic energy agency from Vienna (Daillant and al 2003). (N.C.)

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

    NARCIS (Netherlands)

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

    2002-01-01

    A substantial amount of carbon is emitted by terrestrial vegetation as biogenic volatile organic compounds (VOC), which contributes to the oxidative capacity of the atmosphere, to particle production and to the carbon cycle. With regard to the carbon budget of the terrestrial biosphere, a release of

  6. Dissolved Organic Carbon 14C in Southern Nevada Groundwater and Implications for Groundwater Travel Times

    Energy Technology Data Exchange (ETDEWEB)

    Hershey, Ronald L.; Fereday, Wyall; Thomas, James M

    2016-08-01

    Dissolved inorganic carbon (DIC) carbon-14 (14C) ages must be corrected for complex chemical and physical reactions and processes that change the amount of 14C in groundwater as it flows from recharge to downgradient areas. Because of these reactions, DIC 14C can produce unrealistically old ages and long groundwater travel times that may, or may not, agree with travel times estimated by other methods. Dissolved organic carbon (DOC) 14C ages are often younger than DIC 14C ages because there are few chemical reactions or physical processes that change the amount of DOC 14C in groundwater. However, there are several issues that create uncertainty in DOC 14C groundwater ages including limited knowledge of the initial (A0) DOC 14C in groundwater recharge and potential changes in DOC composition as water moves through an aquifer. This study examines these issues by quantifying A0 DOC 14C in recharge areas of southern Nevada groundwater flow systems and by evaluating changes in DOC composition as water flows from recharge areas to downgradient areas. The effect of these processes on DOC 14C groundwater ages is evaluated and DOC and DIC 14C ages are then compared along several southern Nevada groundwater flow paths. Twenty-seven groundwater samples were collected from springs and wells in southern Nevada in upgradient, midgradient, and downgradient locations. DOC 14C for upgradient samples ranged from 96 to 120 percent modern carbon (pmc) with an average of 106 pmc, verifying modern DOC 14C ages in recharge areas, which decreases uncertainty in DOC 14C A0 values, groundwater ages, and travel times. The HPLC spectra of groundwater along a flow path in the Spring Mountains show the same general pattern indicating that the DOC compound composition does not change along this flow path. Although DOC concentration decreases from recharge-area to downgradient groundwater, the organic compounds are similar, indicating that DOC 14C is unaffected by other processes such as microbial

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

    OpenAIRE

    García Abuín, Alicia

    2012-01-01

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

  8. The optimization of the estimation of carbon-14 in urine

    International Nuclear Information System (INIS)

    The urinalysis method for carbon-14 currently used by the bioassay laboratory of the Dosimetric Research Branch at CRNL has been tested and optimized for both sensitivity and efficiency. Urine is first treated with an enzyme that catalyses the hydrolysis of urea, the major carbon-containing component of urine; carbon dioxide is then liberated by the measured addition of excess acid and collected in 2-aminoethanol. The aminoethanol can be directly counted by the addition of a liquid scintillation cocktail. This method can be used to measure both the specific activity, (Bq/g-carbon) or the total activity of carbon-14 released from the urine sample

  9. Synthesis of carbon black/carbon nitride intercalation compound composite for efficient hydrogen production.

    Science.gov (United States)

    Wu, Zhaochun; Gao, Honglin; Yan, Shicheng; Zou, Zhigang

    2014-08-21

    The photoactivity of g-C3N4 is greatly limited by its high recombination rate of photogenerated carriers. Coupling g-C3N4 with other materials has been demonstrated to be an effective way to facilitate the separation and transport of charge carriers. Herein we report a composite of conductive carbon black and carbon nitride intercalation compound synthesized through facile one-step molten salt method. The as-prepared carbon black/carbon nitride intercalation compound composite was characterized by X-ray diffraction (XRD) and transmission electron microscopy (TEM), UV-vis absorption spectrum and photoluminescence spectroscopy (PL). The carbon black nanoparticles, homogeneously dispersed on the surface of carbon nitride intercalation compound, efficiently enhanced separation and transport of photogenerated carriers, thus improving the visible-light photocatalytic activity. The composite of 0.5 wt% carbon black and carbon nitride intercalation compound exhibited a H2 production rate of 68.9 μmol h(-1), which is about 3.2 times higher than hydrogen production on pristine carbon nitride intercalation compound.

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

    Science.gov (United States)

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

    2016-04-01

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

  11. Analytical Validation of Accelerator Mass Spectrometry for Pharmaceutical Development: the Measurement of Carbon-14 Isotope Ratio.

    Energy Technology Data Exchange (ETDEWEB)

    Keck, B D; Ognibene, T; Vogel, J S

    2010-02-05

    Accelerator mass spectrometry (AMS) is an isotope based measurement technology that utilizes carbon-14 labeled compounds in the pharmaceutical development process to measure compounds at very low concentrations, empowers microdosing as an investigational tool, and extends the utility of {sup 14}C labeled compounds to dramatically lower levels. It is a form of isotope ratio mass spectrometry that can provide either measurements of total compound equivalents or, when coupled to separation technology such as chromatography, quantitation of specific compounds. The properties of AMS as a measurement technique are investigated here, and the parameters of method validation are shown. AMS, independent of any separation technique to which it may be coupled, is shown to be accurate, linear, precise, and robust. As the sensitivity and universality of AMS is constantly being explored and expanded, this work underpins many areas of pharmaceutical development including drug metabolism as well as absorption, distribution and excretion of pharmaceutical compounds as a fundamental step in drug development. The validation parameters for pharmaceutical analyses were examined for the accelerator mass spectrometry measurement of {sup 14}C/C ratio, independent of chemical separation procedures. The isotope ratio measurement was specific (owing to the {sup 14}C label), stable across samples storage conditions for at least one year, linear over 4 orders of magnitude with an analytical range from one tenth Modern to at least 2000 Modern (instrument specific). Further, accuracy was excellent between 1 and 3 percent while precision expressed as coefficient of variation is between 1 and 6% determined primarily by radiocarbon content and the time spent analyzing a sample. Sensitivity, expressed as LOD and LLOQ was 1 and 10 attomoles of carbon-14 (which can be expressed as compound equivalents) and for a typical small molecule labeled at 10% incorporated with {sup 14}C corresponds to 30 fg

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

    NARCIS (Netherlands)

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

    2015-01-01

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

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

    DEFF Research Database (Denmark)

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

    2012-01-01

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

  14. Increased root exudation of 14C-compounds by sorghum seedlings inoculated with nitrogen-fixing bacteria

    International Nuclear Information System (INIS)

    Organic components leaked from Sorghum bicolor seedlings ('root exudates') were examined by recovering 14C labelled compounds from root solutions of seedlings inoculated with Azospirillum brasilense, Azotobacter vinelandii or Klebsiella pneumoniae nif-. Up to 3.5% of the total 14C recovered from shoots, roots, and nutrient solutions was found in the root solutions. Inoculation with Azospirillum and Azotobacter increased the amounts of 14C and decreased the amounts of carbohydrates in the root solutions. When sucrose was added as a carbon source for the bacteria, the increase of 14C in the solutions did not occur. Quantities of 14C found in the root solutions were proportional to amounts of mineral nitrogen supplied to the plants. Bacterial growth also was proportional to nitrogen levels. When sorghum plants were grown in soil and labelled with 14CO2, about 15% of the total 14C recovered within 48 hours exposure was found in soil leachates. (orig.)

  15. The preparation of glucose uniformly labelled with carbon-14

    International Nuclear Information System (INIS)

    The plant, (Zea mais, L) and culture conditions for an optimum production of glucose has been chosen. To achieve the labelling of glucose, photosynthesis and carboxylation are carried on, under an artificial atmosphere of 14CO2 produced from 14C-barium carbonate. Following photosynthesis the sugars are extracted, and then the extract purified by several methods. The purified glucose is finally, degraded and the specific radioactivity is determined in each of its carbon atoms. (Author) 37 refs

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

    Science.gov (United States)

    Costuas, Karine

    2015-01-01

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

  17. Synthesis of carbon-14 labeled Taxol (paclitaxel)

    International Nuclear Information System (INIS)

    Reductive cleavage of the C13 side chain of Taxol (1, paclitaxel) followed by regioselective silylation gave 7-triethylsilylbaccatin III (4). 3-O-Triethysilylation of 5 and subsequent reaction with benzoyl chloride-C7-14C gave azetidinone 7. Coupling of 4 and 7 followed by deprotection gave 1.26 g of Taxol-N3'-14C (11) having a specific activity of 26.5 mCi/mmol and a radiochemical purity of 95%. (author)

  18. Preferential site occupation in Y and La substituted Pr2Fe14B intermetallic compounds

    International Nuclear Information System (INIS)

    The crystal structure of Y and La substituted Pr2Fe14B intermetallic compounds has been determined by high resolution neutron time-of-flight powder diffraction. A model which takes into account the rare-earth site occupancies and the measured magnetic anisotropy in Pr2Fe14B and Nd2Fe14B indicates that the contribution of the 4f site anisotropy to the total axial anisotropy is larger than that of the 4g site in Nd2Fe14B compounds. In Pr2Fe14B compounds, however, the 4f and 4g site anisotropies are equal. (orig.)

  19. Irreversible adsorption of phenolic compounds by activated carbons

    International Nuclear Information System (INIS)

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

  20. Irreversible adsorption of phenolic compounds by activated carbons

    Energy Technology Data Exchange (ETDEWEB)

    Grant, T.M.; King, C.J.

    1988-12-01

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

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

    Science.gov (United States)

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

    1981-01-01

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

  2. Fate of 14C-labelled compounds in marine environment

    International Nuclear Information System (INIS)

    Model ecosystems have played an important role in predicting environmental behavior of agrochemicals. The microcosms used in these studies generally include soil units containing usual biotic components common for that ecosystem. In present studies, scope of two such ecosystems has been extended to study the fate of 14C-labelled pesticides in marine environment. 14C-labelled pesticides used in these studies were chlorpyrifos, DDT and HCH. Two systems were developed in laboratory simulating marine environment to study the fate of these pesticides. The first system was developed in an all glass aquarium tank with marine sediments, seawater, clams and algae and is referred to as marine ecosystem. The second system was developed to permit the total 14C-mass balance studies. It contained marine sediments under moist (60% water holding capacity) or flooded conditions and it is referred to as continuous flow system. Fate of 14C-DDT was studied in marine ecosystem while degradation of 14C-chlorpyrifos and 14C-HCH was studied in continuous flow system. 14C-DDT did not bioaccumulate in clams while at the end of 60 days 50% of the applied 14C-activity was present in sediment fraction of marine ecosystem. 14C-HCH degradation showed about 22-26% mineralization while 45-55% of the applied activity was recovered as organic volatiles. No significant bound residues were formed. 14C-chorpyrifos underwent considerable degradation in marine environment. TCP was the major degradation product. (author)

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

    Science.gov (United States)

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

    2010-01-01

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

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

    Energy Technology Data Exchange (ETDEWEB)

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

    2012-01-01

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

  5. Stable carbon isotope ratios of ambient aromatic volatile organic compounds

    Science.gov (United States)

    Kornilova, Anna; Huang, Lin; Saccon, Marina; Rudolph, Jochen

    2016-09-01

    Measurements of mixing ratios and stable carbon isotope ratios of aromatic volatile organic compounds (VOC) in the atmosphere were made in Toronto (Canada) in 2009 and 2010. Consistent with the kinetic isotope effect for reactions of aromatic VOC with the OH radical the observed stable carbon isotope ratios are on average significantly heavier than the isotope ratios of their emissions. The change of carbon isotope ratio between emission and observation is used to determine the extent of photochemical processing (photochemical age, ∫ [OH]dt) of the different VOC. It is found that ∫ [OH]dt of different VOC depends strongly on the VOC reactivity. This demonstrates that for this set of observations the assumption of a uniform ∫ [OH]dt for VOC with different reactivity is not justified and that the observed values for ∫ [OH]dt are the result of mixing of VOC from air masses with different values for ∫ [OH]dt. Based on comparison between carbon isotope ratios and VOC concentration ratios it is also found that the varying influence of sources with different VOC emission ratios has a larger impact on VOC concentration ratios than photochemical processing. It is concluded that for this data set the use of VOC concentration ratios to determine ∫ [OH]dt would result in values for ∫ [OH]dt inconsistent with carbon isotope ratios and that the concept of a uniform ∫ [OH]dt for an air mass has to be replaced by the concept of individual values of an average ∫ [OH]dt for VOC with different reactivity.

  6. Reactions between sodium and various carbon bearing compounds

    International Nuclear Information System (INIS)

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

  7. 14,15N beam from cyanide compounds

    International Nuclear Information System (INIS)

    We report here on the direct generation of a CN− ion beam for the production of a N ion beam to be used in nuclear astrophysics measurements. The procedure relies on the production of CN− ion beam with a SNICS source starting from several appropriate substrates containing CN− triple bond. Several of the investigated substrates showed a higher beam intensity with respect to the common N beam production from a cathode of BN plus graphite. Best results in terms of analyzed beam intensity were observed with K3Fe(CN)6 and KSCN cathodes. Use of the latter compound is particularly appealing because of the easy availability of mass-15 enriched molecule.

  8. Carbon-14 geochemistry at the Savannah River Site

    Energy Technology Data Exchange (ETDEWEB)

    Roberts, Kimberly A.; Kaplan, Daniel I.

    2013-05-10

    Carbon-14 is among the key radionuclides driving risk at the E-Area Low-Level Waste Disposal Facility on the Savannah River Site (SRS). Much of this calculated risk is believed to be the result of having to make conservative assumptions in risk calculations because of the lack of site-specific data. The original geochemical data package (Kaplan 2006) recommended that performance assessments and composite analyses for the SRS assume that {sup 14}C did not sorbed to sediments or cementitious materials, i.e., that C-14 K{sub d} value (solid:liquid concentration ratio) be set to 0 mL/g (Kaplan 2006). This recommendation was based primarily on the fact that no site-specific experimental work was available and the assumption that the interaction of anionic {sup 14}C as CO{sub 2}{sup 2-}) with similarly charged sediments or cementitious materials would be minimal. When used in reactive transport equations, the 0 mL/g Kd value results in {sup 14}C not interacting with the solid phase and moving quickly through the porous media at the same rate as water. The objective of this study was to quantify and understand how aqueous {sup 14}C, as dissolved carbonate, sorbs to and desorbs from SRS sediments and cementitious materials. Laboratory studies measuring the sorption of {sup 14}C, added as a carbonate, showed unequivocally that {sup 14}C-carbonate K{sub d} values were not equal to 0 mL/g for any of the solid phases tested, but they required several months to come to steady state. After six months of contact, the apparent K{sub d} values for a clayey sediment was 3,000 mL/g, for a sandy sediment was 10 mL/g, for a 36-year-old concrete was 30,000 mL/g, and for a reducing grout was 40 mL/g. Furthermore, it was demonstrated that (ad)sorption rates were appreciably faster than desorption rates, indicating that a kinetic sorption model, as opposed to the steady-state K{sub d} model, may be a more accurate description of the {sup 14}C-carbonate sorption process. A second study

  9. Thermal Expansion Anomaly of Tb2Fe14Cr3 Compound

    Institute of Scientific and Technical Information of China (English)

    HAO Yan-Ming; HE Xiao-Hong; AN Li-Qun; Fu Bin

    2008-01-01

    We investigate the thermal expansion property of the Tb2Fe14Cr3 compound by means of x-ray diffraction.The result shows that the Tb2Fe14Cr3 compound has a hexagonal Th2Ni17-type structure.Negative thermal expansion is found in the Tb2Fe14Cr3 compound from 296 to 493K by x-ray dilatometry.The coefficient of the average thermal expansion is (a)=-2.82×10-5 K-1.In the temperature range 493-692K,the coefficient of the average thermal expansion is (a)=1.59×10-5 K-1.The physical mechanism of thermal expansion anomaly of the Tb2Fe14Cr3 compound is discussed according to the temperature dependence of magnetization measured by a superconducting quantum interference device.

  10. Dissolved Organic Carbon 14C in Southern Nevada Groundwater and Implications for Groundwater Travel Times

    Energy Technology Data Exchange (ETDEWEB)

    Hershey, Ronald L. [Nevada University, Reno, NV (United States). Desert Research Institute; Fereday, Wyall [Nevada University, Reno, NV (United States). Desert Research Institute; Thomas, James M [Nevada University, Reno, NV (United States). Desert Research Institute

    2016-08-01

    Dissolved inorganic carbon (DIC) carbon-14 (14C) ages must be corrected for complex chemical and physical reactions and processes that change the amount of 14C in groundwater as it flows from recharge to downgradient areas. Because of these reactions, DIC 14C can produce unrealistically old ages and long groundwater travel times that may, or may not, agree with travel times estimated by other methods. Dissolved organic carbon (DOC) 14C ages are often younger than DIC 14C ages because there are few chemical reactions or physical processes that change the amount of DOC 14C in groundwater. However, there are several issues that create uncertainty in DOC 14C groundwater ages including limited knowledge of the initial (A0) DOC 14C in groundwater recharge and potential changes in DOC composition as water moves through an aquifer. This study examines these issues by quantifying A0 DOC 14C in recharge areas of southern Nevada groundwater flow systems and by evaluating changes in DOC composition as water flows from recharge areas to downgradient areas. The effect of these processes on DOC 14C groundwater ages is evaluated and DOC and DIC 14C ages are then compared along several southern Nevada groundwater flow paths. Twenty-seven groundwater samples were collected from springs and wells in southern Nevada in upgradient, midgradient, and downgradient locations. DOC 14C for upgradient samples ranged from 96 to 120 percent modern carbon (pmc) with an average of 106 pmc, verifying modern DOC 14C ages in recharge areas, which decreases uncertainty in DOC 14C A0 values, groundwater ages, and travel times. The HPLC spectra of groundwater along a flow path in the Spring Mountains show the same general pattern indicating that the DOC compound composition does not change along this flow path

  11. Carbon 14 dating method; Methode de datation par le carbone 14

    Energy Technology Data Exchange (ETDEWEB)

    Fortin, Ph

    2000-07-01

    This document gives a first introduction to {sup 14}C dating as it is put into practice at the radiocarbon dating centre of Claude-Bernard university (Lyon-1 univ., Villeurbanne, France): general considerations and recalls of nuclear physics; the {sup 14}C dating method; the initial standard activity; the isotopic fractioning; the measurement of samples activity; the liquid-scintillation counters; the calibration and correction of {sup 14}C dates; the preparation of samples; the benzene synthesis; the current applications of the method. (J.S.)

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

    Energy Technology Data Exchange (ETDEWEB)

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

    2014-01-01

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

  13. Transfer of 14C to prenatal and neonatal rats from their mothers exposed to 14C compounds by ingestion

    International Nuclear Information System (INIS)

    The transfer of 14C through placenta or milk was investigated and the radiation dose to fetal and newborn rats was estimated. Female rats at gestational stages or after delivery were exposed to 14C in the form of sodium bicarbonate, thymidine and lysine by a single ingestion. Radioactivity in maternal tissues and conceptuses (placenta, fetal membrane and fetus) and in the newborn was determined at various times after ingestion. After exposure to these 14C compounds, there was no significant difference between the 14C concentration in the fetus and that in the maternal tissues, suggesting that the placenta has no effect in preventing or accelerating the placental transfer of 14C. The concentration and content of 14C in the fetus and newborn were, however, dependent on the chemical form of 14C and on the prenatal or neonatal stage at the time of ingestion. The result of the dose estimation showed that 14C-lysine gave significantly higher prenatal and neonatal doses than 14C-sodium bicarbonate or 14C-thymidine. (author)

  14. Progressive extraction method applied to isotopic exchange of carbon-14

    International Nuclear Information System (INIS)

    Isotopic exchange in natural settings is essentially an irreversible process, so that it progresses continuously until there is complete isotopic equilibrium. In soils, this process involves interaction between isotopes in the liquid and solid phases, and complete isotopic equilibrium may take a very long time. Measurements after partial isotopic exchange have been used to characterize the labile fraction of elements in soils. We describe a method to characterize the extent of isotopic exchange, with application here to incorporation of inorganic carbon-14 (14C) into mineral carbonates and organic matter in soils. The procedure uses a continuous addition of extractant, acid, or H2O2in the examples presented here, coupled with sequential sampling. The method has been applied to demonstrate the degree of isotopic exchange in soil. The same strategy could be applied to many other elements, including plant nutrients. (author)

  15. A detective from the past called carbon 14

    International Nuclear Information System (INIS)

    The analysis is carried out using Radiometry or Accelerator mass spectrometry. After the system allowing to date the age of any organic rest - whether a fossil, a wood fragment, a parchment or a seed - is an isotope called carbon-14. An atom that comes from reactions nuclear produced in the atmosphere and cosmic-ray-induced they interact with oxygen to form carbon dioxide. This element they absorb it plants in photosynthesis and then passes to the animals remained almost unchanged during the life of the organism. to the meet the initial ratio of c-14 that had been in the atmosphere before his death, the remains that are left in it determine the elapsed time. (Author)

  16. Carbon budget of a marine phytoplankton-herbivore system with carbon-14 as a tracer

    Energy Technology Data Exchange (ETDEWEB)

    Copping, A.E.; Lorenzen, C.J.

    1980-09-01

    Adult female and stage V Calanus pacificus were fed /sup 14/C-labeled phytoplankton in the laboratory in the form of monospecific cultures and natural populations. A carbon budget was constructed by following the /sup 14/C activity and the specific activity, over 48 h, in the phytoplankton, copepod, dissolved organic, dissolved inorganic, and fecal carbon compartments. The average incorporation of carbon into the copepod's body was 45% of the phytoplankton carbon available. Of the phytoplankton carbon, 27% appeared as dissolved organic carbon, 24% as dissolved inorganic carbon, and 3 to 4% in the form of fecal pellets. All of the tracer was recovered at the end of the experiments. The specific activity of the phytoplankton compartment was constant throughout each experiment. The other compartments had initial specific activities of zero, or close to zero, and increased throughout the experiment. In most experiments, the copepod specific activity equalled that of the phytoplankton at the end of 48 h, while the dissolved organic carbon, dissolved inorganic carbon, and fecal specific activities remained well below that of the phytoplankton.

  17. Rietveld Refinement of New Ternary Compound Al14Dy5Si

    Institute of Scientific and Technical Information of China (English)

    2006-01-01

    A new ternary compound Al14Dy5Si was discovered and studied by means of X-ray powder diffraction technique. The ternary compound Al14Dy5Si has a hexagonal BaPb3-type structure, space group R3m(No.166), the lattice parameters a=0.61482(1) nm, c=2.09780(2) nm. The crystal structure of the compound Al14Dy5Si was successfully refined by using Rietveld method from X-ray diffraction data. The R-factors of Rietveld refinement are Rp=0.091 and Rwp=0.120, respectively. The thermal dependence of the magnetization (M-T curves) for the compound was measured by a vibrating sample magnetometer. The experimentally determined magnetic effective paramagnetic moment is μeff=23.22 μB per formula unit (10.36 μB per Dy atom).

  18. Radiative Neutron Capture on Carbon-14 in Effective Field Theory

    OpenAIRE

    Rupak, Gautam; Fernando, Lakma; Vaghani, Akshay

    2012-01-01

    The cross section for radiative capture of neutron on carbon-14 is calculated using the model-independent formalism of halo effective field theory. The dominant contribution from E1 transition is considered, and the cross section is expressed in terms of elastic scattering parameters of the effective range expansion. Contributions from both resonant and non-resonant interaction are calculated. Significant interference between these leads to a capture contribution that deviates from simple Bre...

  19. Increased root exudation of /sup 14/C-compounds by sorghum seedlings inoculated with nitrogen-fixing bacteria

    Energy Technology Data Exchange (ETDEWEB)

    Lee, K.J. (Institute of Forest Genetics, Suweon (Republic of Korea)); Gaskins, M.H. (Florida Univ., Gainesville (USA). Dept. of Agriculture)

    1982-01-01

    Organic components leaked from Sorghum bicolor seedlings ('root exudates') were examined by recovering /sup 14/C labelled compounds from root solutions of seedlings inoculated with Azospirillum brasilense, Azotobacter vinelandii or Klebsiella pneumoniae nif-. Up to 3.5% of the total /sup 14/C recovered from shoots, roots, and nutrient solutions was found in the root solutions. Inoculation with Azospirillum and Azotobacter increased the amounts of /sup 14/C and decreased the amounts of carbohydrates in the root solutions. When sucrose was added as a carbon source for the bacteria, the increase of /sup 14/C in the solutions did not occur. Quantities of /sup 14/C found in the root solutions were proportional to amounts of mineral nitrogen supplied to the plants. Bacterial growth also was proportional to nitrogen levels. When sorghum plants were grown in soil and labelled with /sup 14/CO/sub 2/, about 15% of the total /sup 14/C recovered within 48 hours exposure was found in soil leachates.

  20. Synthesis of a polycyclic aromatic hydrocarbon marked with carbon-14: (b, d e f) dibenzo-chrysene {sup 14}C-7,14; Synthese d'un hydrocarbure aromatique polycyclique marque au carbone 14: le dibenzo (b, d e f) chrysene {sup 14}C-7,14

    Energy Technology Data Exchange (ETDEWEB)

    Chatelain, G. [Commissariat a l' Energie Atomique, Saclay (France). Centre d' Etudes Nucleaires

    1965-07-01

    (b, d e f) dibenzo-chrysene C-7,14 has been synthesized from radioactive carbon dioxide and the organic magnesium compound derived from 1,5 dibromo naphthalene. The product has been purified by a very precise series of fractionated chromatographs on alumina having a chromatographic activity. This has necessitated the development of a special technique. (author) [French] Le dibenzo (b, d e f) chrysene 14C-7,14 a ete synthetise au depart de gaz carbonique radioactif et de bis-organomagnesien derive du dibromo-1,5 naphtalene. Le produit a ete purifie par une serie de chromatographies fractionnees sur alumine d'activite chromatographique tres precise. Ceci a fait l'objet d'une mise au point de technique. (auteur)

  1. A detective from the past called carbon 14; Un detective del pasado llamado carbono 14

    Energy Technology Data Exchange (ETDEWEB)

    Trintan, R. M.

    2015-07-01

    The analysis is carried out using Radiometry or Accelerator mass spectrometry. After the system allowing to date the age of any organic rest - whether a fossil, a wood fragment, a parchment or a seed - is an isotope called carbon-14. An atom that comes from reactions nuclear produced in the atmosphere and cosmic-ray-induced they interact with oxygen to form carbon dioxide. This element they absorb it plants in photosynthesis and then passes to the animals remained almost unchanged during the life of the organism. to the meet the initial ratio of c-14 that had been in the atmosphere before his death, the remains that are left in it determine the elapsed time. (Author)

  2. Thermal expansion anomaly and spontaneous magnetostriction of Dy2AlFe14Mn2 compound

    Institute of Scientific and Technical Information of China (English)

    WANG Hai-yun; ZHAO Miao; GAO Yan; ZHOU Yan; FU Bin; YAN Da-li

    2006-01-01

    The structure and magnetic properties of Dy2AlFe14Mn2 compound were investigated by X-ray diffractometry and magnetization measurements. Dy2AlFe14Mn2 compound has a hexagonal Th2Ni17-type structure. Zero thermal expansion and negative thermal expansion were found in Dy2AlFe14Mn2 compound in the temperature range from 184 to 264 K, and from 264 to 383 K, respectively, by X-ray dilatometry. The spontaneous magnetostrictive deformations from 104 to 400 K were calculated. The results show that the spontaneous volume magnetostrictive deformation increases firstly with increasing temperature, and then decreases with furtther increasing temperature.

  3. Adsorption of Purine Compounds in Beer with Activated Carbon Prepared from Beer Lees

    OpenAIRE

    Shibata, Junji; MURAYAMA, Norihiro; TAKEYAMA, Masato

    2009-01-01

    Six hundred thousand tons of beer lees are discharged annually in Japanese breweries. It is well known that purine compounds are one of substances which cause the gout and beer especially contains a lot of purine compounds such as adenosine, adenosine 5’-phosphate and so on, compared with the other alcoholic drinks. The application of activated carbon prepared from beer lees was investigated in order to remove purine compounds in beer. The reuse and recycling of beer lees to activated carbon ...

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

    International Nuclear Information System (INIS)

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

  5. 14N NQR investigation of some thermochromic and photochromic salicylideneanilines and related compounds

    Science.gov (United States)

    Hadjoudis, E.; Milia, F.; Seliger, J.; Zagar, V.; Blinc, R.

    1991-09-01

    The temperature dependence of the 14N NQR frequencies have been measured in a series of thermochromic and photochromic salicylideneanilines and related compounds using nuclear quadrupole double resonance. The results show that, in agreement with previous measurements, there is a fast exchange between inequivalent sites in the OH…N bond. The energy difference Δ E of the two proton sites was calculated for all the compounds and shows that it depends on their thermochromic behavior which is connected with the structure of the compounds.

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

    Lifescience Database Archive (English)

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

  7. 8-Hydroxynaphthalene-1,4-dione derivative as novel compound for glioma treatment.

    Science.gov (United States)

    Zagotto, Giuseppe; Redaelli, Marco; Pasquale, Riccardo; D'Avella, Domenico; Cozza, Giorgio; Denaro, Luca; Pizzato, Francesca; Mucignat-Caretta, Carla

    2011-04-01

    Malignant gliomas continue to demand the search for improved chemotherapeutic solutions. In this work the results of a preliminary in vitro screening performed on a small library of compounds are disclosed. As a result 2-(2,4-dihydroxyphenyl)-8-hydroxy-1,4-naphthoquinone emerged as a promising therapeutic lead. PMID:21353776

  8. Carbon isotopic study of individual alcohol compounds in modern sediments from Nansha Islands sea area, China

    Institute of Scientific and Technical Information of China (English)

    段毅; 文启彬; 郑国东; 罗斌杰

    1997-01-01

    Carbon isotopic compositions of individual n-alkanols and sterols in modern sediments from the Nan-sha Islands sea area are measured after derivatization to trimethylsilyl ethers by the new isotopic analytical technique of GC/C/IRMS. The effects of the three added silyl carbon atoms in every alcohol molecule on these compound isotopic compositions and the characteristics of their carbon isotopic compositions are studied. Then their biological sources are discussed using their carbon isotopic compositions.

  9. Nitrogen Additions Increase the Diversity of Carbon Compounds Degraded by Fungi in Boreal Forests

    Science.gov (United States)

    Gartner, T. B.; Turner, K. M.; Treseder, K. K.

    2004-12-01

    Boreal forest soils in North America harbor a large reservoir of organic C, and this region is increasingly exposed to long-range atmospheric N transport from Eurasia. By examining the responses of decomposers to N deposition in these forests, we hope to improve predictions of the fate of boreal carbon pools under global change. We tested the hypothesis that the functional diversity of decomposer fungi would increase under N fertilization in boreal forests where fungal growth was otherwise N-limited, owing to a reduction in competitive exclusion of fungal groups. We collected soil and leaf litter from three Alaskan sites that represent different successional stages at 5, 17, or 80 years following severe forest fire. Each site had been exposed for two years to nitrogen and phosphorus fertilization in a factorial design, with four plots per treatment. Nutrient limitation of fungal growth varied depending on successional stage. The standing hyphal length of decomposer fungi in soil (i.e. Ascomycota and Basidiomycota) responded to neither N nor P in the 5-year old site, increased under N fertilization in the 17-year old site, and increased where N and P was added simultaneously in the 80-year old site (site x N x P interaction: P = 0.001). We used BIOLOG microplates for filamentous fungi to obtain an index of the diversity of carbon use by decomposer fungi; each of 95 wells of these plates contains a different carbon-based compound, as well as a dye that changes color upon metabolism of the compound. Saline leaf litter extracts were mixed with fungal growth medium and then added to the microplates. The number of wells displaying metabolic activity was counted following incubation for five days. We found that N fertilization raised the average number of positive wells per plate from 14 to 27 (P = 0.012), with no significant differences in responses among sites. Phosphorus additions did not alter functional diversity of fungi in any site. Since increases in functional

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

    Science.gov (United States)

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

    2016-04-01

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

  11. Crystal structure and Rietveld refinement of the new ternary compound Al14Nd5Si

    Institute of Scientific and Technical Information of China (English)

    2008-01-01

    The new ternary compound Al14Nd5Si has been studied by means of the X-ray powder diffraction technique and the Rietveld method.The ternary compound Al14NdsSi has a hexagonal Ni3Sn-type structure with space group P63/mmc (No.194),the lattice parameters are a=0.64470 (2) nm and c = 0.45926 (1) nm.The Smith and Snyder figure of merit for the index,FN,is F30 = 97.8 (30).The X-ray diffraction data indicated that the crystal structure of the compound Al14Nd5Si has been successfully refined by the Rietveld method.The R-factors of Rietreid refinement are Rp = 0.088 and Rwp = 0.120,respectively.The thermal dependence of magnetization for the compound was measured by a vibrating sample magnetometer.The experimentally determined magnetic effective paramagnetic moment is μeff=3.60 μB per Nd atom.The paramagnetic Currie temperature θp = -33.7 K was also obtained from the Currie-Weiss law.

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

    Science.gov (United States)

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

    2016-01-01

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

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

    Science.gov (United States)

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

    2016-01-01

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

  14. Adsorption of aromatic compounds from the biodegradation of azo dyes on activated carbon

    Science.gov (United States)

    Faria, P. C. C.; Órfão, J. J. M.; Figueiredo, J. L.; Pereira, M. F. R.

    2008-03-01

    The adsorption of three selected aromatic compounds (aniline, sulfanilic acid and benzenesulfonic acid) on activated carbons with different surface chemical properties was investigated at different solution pH. A fairly basic commercial activated carbon was modified by means of chemical treatment with HNO 3, yielding an acid activated carbon. The textural properties of this sample were not significantly changed after the oxidation treatment. Equilibrium isotherms of the selected compounds on the mentioned samples were obtained and the results were discussed in relation to their surface chemistry. The influence of electrostatic and dispersive interactions involved in the uptake of the compounds studied was evaluated. The Freundlich model was used to fit the experimental data. Higher uptakes are attained when the compounds are present in their molecular form. In general, adsorption was disfavoured by the introduction of oxygen-containing groups on the surface of the activated carbon.

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

    Science.gov (United States)

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

    2012-08-01

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

  16. Biosphere structure, carbon sequestering potential and the atmospheric C-14 carbon record

    Energy Technology Data Exchange (ETDEWEB)

    Goudriaan, J.

    1992-08-01

    The behaviour of a numerical model for the global carbon cycle is elucidated by a simple analytical model for the biosphere. In the period 1980-1990 the ocean is estimated to have absorbed 33% of the total CO{sub 2} emission to the atmosphere in that same period. Net deforestation was responsible for 12-17% of this total emission rate, whereas the CO{sub 2}-fertilization effect caused a re-absorption of 20-25%. Aggregation of the above-ground biosphere into a single pool in the model caused an overestimation of the CO{sub 2}-fertilization effect. Also, the estimate of this rate increased when the fraction of carbon assumed to remain after the transformation of litter into humus was increased, but the rate was little influenced by the model structure for soil organic carbon. A larger estimate for carbon uptake in the biosphere (Tans, Fung, and Takahashi, 1990) must be compensated by a reduced uptake in the ocean to arrive at a carbon balance. To do this, either the exchange rate between the upper mixed ocean layer and deep sea, or between ocean surface and atmosphere, should be reduced. In addition, a good match to the observed time-course of C-14 carbon in the atmosphere must be preserved by the model. The C-14 time-course did not remain well-matched if the atmosphere-ocean surface exchange was reduced, but it was hardly disturbed at all if the exchange rate with the deep sea was reduced.

  17. The preparation of glucose uniformly labelled with carbon-14; Preparacion de glucosa uniformemente marcada con carbono-14

    Energy Technology Data Exchange (ETDEWEB)

    Garcia, M. D.; Suarez, C.; Rodrigo, M. E.

    1978-07-01

    The plant, (Zea mais, L) and culture conditions for an optimum production of glucose has been chosen. To achieve the labelling of glucose, photosynthesis and carboxylation are carried on, under an artificial atmosphere of 14CO{sub 2} produced from 14{sup C}-barium carbonate. Following photosynthesis the sugars are extracted, and then the extract purified by several methods. The purified glucose is finally, degraded and the specific radioactivity is determined in each of its carbon atoms. (Author) 37 refs.

  18. Electronic structure and magnetism of AFe2 compounds with C14 and C15 laves structures

    International Nuclear Information System (INIS)

    The d-band densities of states are calculated by the recursion method for the paramagnetic AFe2 compounds with C14 and C15 structures, where A is occupied by 3d (Sc, Ti, V), 4d (Y, Zr, Nb) or 5d (Lu, Hf, Ta) series' elements. The densities of states of the ferromagnetic and antiferromagnetic (Zr/sub 1-x/Nb/sub x/)Fe2 compounds with C15 and C14 structures are calculated. The pseudobinary systems are treated within a virtual crystal approximation. The trends of the crystal structures are related to the d electron number around the A site. Magnetic moment and spontaneous volume magnetostriction are calculated on the basis of the Stoner theory. (author)

  19. Mechanisms of Microwave Absorption in Carbon Compounds from Shungite

    Directory of Open Access Journals (Sweden)

    S. Emelyanov

    2013-12-01

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

  20. Mechanisms of Microwave Absorption in Carbon Compounds from Shungite

    OpenAIRE

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

    2013-01-01

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

  1. Thermal Expansion Anomaly and Spontaneous Magnetostriction of Y2Fe14Al3Compound

    Institute of Scientific and Technical Information of China (English)

    HAO Yan-Ming; ZHANG Yan-Yan; JIANG Xin-Yuan; GAO Chun-Jing; WU Yan-Zhao

    2009-01-01

    The structure and magnetic properties of Y2Fe14Al3 compound are investigated by means of x-ray diffraction and magnetization measurements. The Y2Fe14.Al3 compound has a hexagonal Th2Ni17-type structure. Nega-tive thermal expansion is found in Y2Fe14Al3 compound in the temperature range from 403 to 491K by x-ray dilatometry. The coefficient of the average thermal expansion is α = -2.54 × 10-5 K-1. The spontaneous mag-netostrictive deformations from 283 to 470 K are calculated by means of the differences between the experimental values of the lattice parameters and the corresponding values extrapolated from the paramagnetic range. The result shows that the spontaneous volume magnetostrictive deformation ωs decreases from 5.74 × 10-3 to nearly zero with temperature increasing from 283 to 470K, the spontaneous linear magnetostrictive deformation λc along the c-axis is larger than the spontaneous linear magnetostrictive deformation λα in basal-plane in the same temperature below 350K.

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

    Directory of Open Access Journals (Sweden)

    Diego A. Esquivel-Hernández

    2016-05-01

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

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

    Science.gov (United States)

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

    2016-01-01

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

  4. Synthesis of deleobuvir, a potent hepatitis C virus polymerase inhibitor, and its major metabolites labeled with carbon-13 and carbon-14.

    Science.gov (United States)

    Latli, Bachir; Hrapchak, Matt; Chevliakov, Maxim; Li, Guisheng; Campbell, Scot; Busacca, Carl A; Senanayake, Chris H

    2015-05-30

    Deleobuvir, (2E)-3-(2-{1-[2-(5-bromopyrimidin-2-yl)-3-cyclopentyl-1-methyl-1H-indole-6-carboxamido]cyclobutyl}-1-methyl-1H-benzimidazol-6-yl)prop-2-enoic acid (1), is a non-nucleoside, potent, and selective inhibitor of hepatitis C virus NS5B polymerase. Herein, we describe the detailed synthesis of this compound labeled with carbon-13 and carbon-14. The synthesis of its three major metabolites, namely, the reduced double bond metabolite (2) and the acyl glucuronide derivatives of (1) and (2), is also reported. Aniline-(13) C6 was the starting material to prepare butyl (E)-3-(3-methylamino-4-nitrophenyl-(13) C6 )acrylate [(13) C6 ]-(11) in six steps. This intermediate was then used to obtain [(13) C6 ]-(1) and [(13) C6 ]-(2) in five and four more steps, respectively. For the radioactive synthesis, potassium cyanide-(14) C was used to prepare 1-cylobutylaminoacid [(14) C]-(23) via Buchrer-Bergs reaction. The carbonyl chloride of this acid was then used to access both [(14) C]-(1) and [(14) C]-(2) in four steps. The acyl glucuronide derivatives [(13) C6 ]-(3), [(13) C6 ]-(4) and [(14) C]-(3) were synthesized in three steps from the acids [(13) C6 ]-(1), [(13) C6 ]-(2) and [(14) C]-(1) using known procedures. PMID:25964148

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

    Energy Technology Data Exchange (ETDEWEB)

    Irei, Satoshi, E-mail: irei.satoshi@nies.go.jp [Centre for Atmospheric Chemistry, Department of Chemistry, York University, 4700 Keele Street, Toronto, Ontario M3J 1P3 (Canada); Climate Research Division, Atmospheric Science and Technology Directorate, Science and Technology Branch, Environment Canada, 4905 Dufferin Street, Toronto, Ontario M3H 5T4 (Canada); Rudolph, Jochen [Centre for Atmospheric Chemistry, Department of Chemistry, York University, 4700 Keele Street, Toronto, Ontario M3J 1P3 (Canada); Huang, Lin [Climate Research Division, Atmospheric Science and Technology Directorate, Science and Technology Branch, Environment Canada, 4905 Dufferin Street, Toronto, Ontario M3H 5T4 (Canada)

    2013-07-05

    Graphical abstract: -- Highlights: •For GCC–IRMS analysis, an approach avoiding impact of NO{sub 2} on δ{sup 13}C was demonstrated. •Carbon isotope fractionations during derivatizing reactions here were negligible. •Except some labile compounds, the overall bias of the method here was −0.21‰. •Even for the labile compounds, measurement biases ranged +1.2‰ to −1.4‰. •Real sample analysis demonstrates usefulness of the method for fractionation study. -- Abstract: We developed an analytical method for measuring compound-specific stable carbon isotope ratios (δ{sup 13}C) of phenols and nitrophenols in filter samples of particulate organic matter. The method was tested on 13 phenols derivatized with N,O-bis(trimethylsilyl)trifluoroacetamide (BSTFA), together with four nonphenolic compounds. The data obtained by our method required two specific corrections for the determination of valid δ{sup 13}C values: (1) for nitro compounds, the routine correction with use of m/z 46 for the contribution of {sup 12}C{sup 17}O{sup 16}O molecules) to m/z 45 was modified due to impact of NO{sub 2} on the m/z 46 trace, and (2) for the derivatized phenols, measured δ{sup 13}C values were corrected for the shift in δ{sup 13}C due to the addition of carbon atoms from the BSTFA moiety. Analysis of standard-spiked filters showed that overall there was a small compound-dependent bias in the δ{sup 13}C values: the average bias ± the standard error of the mean of −0.21 ± 0.1‰ for the standard compounds tested, except 3-methylcatechol, methylhydroquinone, 4-methyl-2-nitrophenol, and 2,6-dimethyl-4-nitrophenol, whereas the average biases ± the standard errors of the mean for those were +1.2 ± 0.3‰, +1.2 ± 0.2‰, −1.2 ± 0.2‰, and −1.4 ± 0.5‰, respectively, when the injected mass of a derivatized compound exceeded 15 ngC. In situations where such small biases and uncertainties are acceptable, the method described here could be used to obtain valuable

  6. Pharmacokinetic and metabolic study of the compound GYKI-32 594 labelled with 14C

    International Nuclear Information System (INIS)

    Resorption, blood serum level, tissue distribution and elimination of the 14C-labelled antiserotonin drug 1-methyl-9,10-dihydro-lisergic acid (2'-thiazole-2-il/-amid)bimaleinate were investigated in rats. The compound is resorbed both from the stomach and the small intestine (in two hours 22.5% and 83.8%, resp.). The serum level quickly decreases, Tsub(1/2) being 1.4 - 2.8 hours, depending on the administered dose. Cumulative administration does not increase the serum level. The highest activity was found in the liver and kidneys, but in the brain no radioactivity could be detected. Elimination occurred through the urine (31.7%) and the faeces (23.7%); the enterohepatic circulation was not significant. The compound penetrates into the placenta and appears in the mother's milk. Both in the serum and the urine only a minor part (11-15%) of the radioactivity is represented by the original compound; 4 other metabolites are present. (L.E.)

  7. Synthesis of carbon-14 labelled indolic 5HT{sub 1} receptor agonists

    Energy Technology Data Exchange (ETDEWEB)

    Waterhouse, Ian; Cable, K.M.; Fellows, Ian; Wipperman, M.D.; Sutherland, D.R. [Glaxo Wellcome Research and Development, Stevenage (United Kingdom). Isotope Chemistry Unit

    1996-11-01

    Syntheses of carbon-14 labelled versions of indolic 5HT{sub 1} agonists sumatriptan (GR43175), GR40370 and naratriptan (GR85548) are described. Introduction of the label via cyanation of ketoformanilides, formed by oxidative cleavage of an indole ring, ensured incorporation of carbon-14 at the metabolically stable C-2 position of the indole. (author).

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

    Science.gov (United States)

    Irei, Satoshi; Rudolph, Jochen; Huang, Lin

    2013-07-01

    We developed an analytical method for measuring compound-specific stable carbon isotope ratios (δ(13)C) of phenols and nitrophenols in filter samples of particulate organic matter. The method was tested on 13 phenols derivatized with N,O-bis(trimethylsilyl)trifluoroacetamide (BSTFA), together with four nonphenolic compounds. The data obtained by our method required two specific corrections for the determination of valid δ(13)C values: (1) for nitro compounds, the routine correction with use of m/z 46 for the contribution of (12)C(17)O(16)O molecules) to m/z 45 was modified due to impact of NO2 on the m/z 46 trace, and (2) for the derivatized phenols, measured δ(13)C values were corrected for the shift in δ(13)C due to the addition of carbon atoms from the BSTFA moiety. Analysis of standard-spiked filters showed that overall there was a small compound-dependent bias in the δ(13)C values: the average bias±the standard error of the mean of -0.21±0.1‰ for the standard compounds tested, except 3-methylcatechol, methylhydroquinone, 4-methyl-2-nitrophenol, and 2,6-dimethyl-4-nitrophenol, whereas the average biases±the standard errors of the mean for those were +1.2±0.3‰, +1.2±0.2‰, -1.2±0.2‰, and -1.4±0.5‰, respectively, when the injected mass of a derivatized compound exceeded 15 ngC. In situations where such small biases and uncertainties are acceptable, the method described here could be used to obtain valuable information about δ(13)C values. We also analyzed a real filter sample to demonstrate the practical applicability of the method.

  9. Synthesis of Carbon Nanotubes and Volatile Organic Compounds Detection

    Directory of Open Access Journals (Sweden)

    Sobri S.

    2016-01-01

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

  10. Towards a global understanding of vertical soil carbon dynamics: meta-analysis of soil 14C data

    Science.gov (United States)

    hatte, C.; Balesdent, J.; Guiot, J.

    2012-12-01

    Soil represents the largest terrestrial storage mechanism for atmospheric carbon from photosynthesis, with estimates ranging from 1600 Pg C within the top 1 meter to 2350 Pg C for the top 3 meters. These values are at least 2.5 times greater than atmospheric C pools. Small changes in soil organic carbon storage could result in feedback to atmospheric CO2 and the sensitivity of soil organic matter to changes in temperature, and precipitation remains a critical area of research with respect to the global carbon cycle. As an intermediate storage mechanism for organic material through time, the vertical profile of carbon generally shows an age continuum with depth. Radiocarbon provides critical information for understanding carbon exchanges between soils and atmosphere, and within soil layers. Natural and "bomb" radiocarbon has been used to demonstrate the importance and nature of the soil carbon response to climatic and human impacts on decadal to millennial timescales. Radiocarbon signatures of bulk, or chemically or physically fractionated soil, or even of specific organic compounds, offer one of the only ways to infer terrestrial carbon turnover times or test ecosystem carbon models. We compiled data from the literature on radiocarbon distribution on soil profiles and characterized each study according to the following categories: soil type, analyzed organic fraction, location (latitude, longitude, elevation), climate (temperature, precipitation), land use and sampling year. Based on the compiled data, soil carbon 14C profiles were reconstructed for each of the 226 sites. We report here partial results obtained by statistical analyses of portion of this database, i.e. bulk and bulk-like organic matter and sampling year posterior to 1980. We highlight here 14C vertical pattern in relationship with external parameters (climate, location and land use).

  11. Effect of dead carbon on the 14C dating of the speleothem

    Institute of Scientific and Technical Information of China (English)

    CAI Yanjun; Warren Beck; PENG Zicheng; ZHANG Zhaofeng

    2005-01-01

    Based on the comparison of dating results among high-precision TIMS U-series and AMS 14C as well as the published 14C dating results and their band counting ages (i.e. calendar ages), this paper discusses the effect of dead carbon on the speleothem 14C dating. The result shows that the fraction of incorporated dead carbon during the formation of speleothem varies. The change in the fraction of dead carbon would result in big deviation in the 14C age of the speleothem. It is indispensable to take the dead carbon into consideration when dating the speleothem using the 14C method or studying the atmospheric 14C concentration during the past with the speleothem.

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

    Energy Technology Data Exchange (ETDEWEB)

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

    2009-02-15

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

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

    Science.gov (United States)

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

    2016-08-01

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

  14. Effect of industrial fuel combustion on the carbon-14 level of atmospheric CO2

    International Nuclear Information System (INIS)

    As was previously noticed in 1953 by SUESS, the radiocarbon content of atmospheric CO2 was slightly lower in the 20th century (before the increase in the carbon-14 level due to the addition of artificial 14C) than at the time before the beginning of the industrial revolution in the 19th century. An exact knowledge of the magnitude of this effect is of interest in connection with the question of the rate of isotope exchange between atmospheric CO2 and the bicarbonates of the oceans. However, the radiocarbon level in the CO2 of the atmosphere is also subject to natural fluctuations caused by a variable cosmic-ray production rate of carbon-14. To investigate this the authors have cross-correlated sunspot numbers (as indicators of cosmic-ray activity) with the carbon-14 level in wood, and have detected a significant coherence between the two time series. The observed coherence permits an extrapolation of the natural carbon-14 values beyond the time of the beginning of artificial combustion of fossil fuel, around 1880. The results show that the observed small decrease in the carbon-14 level is somewhat affected by the increase of the production rate of carbon-14, as a consequence of relatively low solar activity during the preceding decades. The effect of industrial fuel combustion upon the carbon-14 level of the atmosphere can then be estimated for the Northern Hemisphere to be in the vicinity of -3%. (author)

  15. Covering vertically aligned carbon nanotubes with a multiferroic compound

    KAUST Repository

    Mahajan, Amit

    2014-10-30

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

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

    Directory of Open Access Journals (Sweden)

    Masahiko Hayashi

    2009-08-01

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

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

    OpenAIRE

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

    2004-01-01

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

  18. Laboratory Experiments to Evaluate Matrix Diffusion of Dissolved Organic Carbon Carbon-14 in Southern Nevada Fractured-rock Aquifers

    Energy Technology Data Exchange (ETDEWEB)

    Hershey, Ronald L. [Nevada University, Reno, NV (United States). Desert Research Institute; Fereday, Wyatt [Nevada University, Reno, NV (United States). Desert Research Institute

    2016-05-01

    Dissolved inorganic carbon (DIC) carbon-14 (14C) is used to estimate groundwater ages by comparing the DIC 14C content in groundwater in the recharge area to the DIC 14C content in the downgradient sampling point. However, because of chemical reactions and physical processes between groundwater and aquifer rocks, the amount of DIC 14C in groundwater can change and result in 14C loss that is not because of radioactive decay. This loss of DIC 14C results in groundwater ages that are older than the actual groundwater ages. Alternatively, dissolved organic carbon (DOC) 14C in groundwater does not react chemically with aquifer rocks, so DOC 14C ages are generally younger than DIC 14C ages. In addition to chemical reactions, 14C ages may also be altered by the physical process of matrix diffusion. The net effect of a continuous loss of 14C to the aquifer matrix by matrix diffusion and then radioactive decay is that groundwater appears to be older than it actually is. Laboratory experiments were conducted to measure matrix diffusion coefficients for DOC 14C in volcanic and carbonate aquifer rocks from southern Nevada. Experiments were conducted using bromide (Br-) as a conservative tracer and 14C-labeled trimesic acid (TMA) as a surrogate for groundwater DOC. Outcrop samples from six volcanic aquifers and five carbonate aquifers in southern Nevada were used. The average DOC 14C matrix diffusion coefficient for volcanic rocks was 2.9 x 10-7 cm2/s, whereas the average for carbonate rocks was approximately the same at 1.7 x 10-7 cm2/s. The average Br- matrix diffusion coefficient for volcanic rocks was 10.4 x 10-7 cm2/s, whereas the average for carbonate rocks was less at 6.5 x 10-7 cm2/s. Carbonate rocks exhibited greater variability in

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

    Directory of Open Access Journals (Sweden)

    Bal-Ram Adhikari

    2015-09-01

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

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

    Science.gov (United States)

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

    2015-01-01

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

  1. Report on Carbon-14 generation and release at some of the Hanford reactors

    Energy Technology Data Exchange (ETDEWEB)

    Barton, G.B.

    1964-12-14

    The Hanford graphite-moderated reactors have an enclosed gas circulation system to maintain control of the composition of gas atmosphere in the graphite stack. This investigation was undertaken to answer several questions concerning the generation and release of Carbon-14 in the operation of these graphite moderated reactors. The principle question was: Will an increase in the nitrogen content of the reactor atmosphere increase the release of Carbon-14 sufficiently to create a health hazard. Other questions were: (1) What are the main sources and the main release routes. (2) How much does carbon-14 build up in the graphite in the reactor stack. and (3) Is the total release of carbon-14 to the atmosphere sufficient to enhance the /sup 14/C levels in the vegetation surrounding the reactors.

  2. Synthesis of methyl [(chloro-2 ethyl)-3 nitroso-3 Ureido]-3 Didesoxy-2,3 α-D-Arabino-hexopyrannoside labelled with carbon-14 or carbon-13 (CY 233 - SR 90008)

    International Nuclear Information System (INIS)

    CY 233 (Ecomustine or SR 90098) is a new antitumour nitrosourea: it is characterized by a 2-chloroethylnitrosourea substituent on a dideoxycarbohydrate. It has been labelled with 14C on a) the carbonyl group of the urea in four stages starting with 14COCl2, b) the second carbon of the chloroethyl group in four stages starting with [14C] ethanolamine, and c) on the methyl group on the anomeric centre of the carbohydrate in three stages starting with 14CH3OH. The final position was also labelled with 13C starting with 13CH3OH. These differently labelled compounds are suitable for mechanistic studies of antitumour activity. (author)

  3. Stable Isotopic Evidence for a Pedogenic Origin of Carbonates in Trench 14 near Yucca Mountain, Nevada.

    Science.gov (United States)

    Quade, J; Cerling, T E

    1990-12-14

    Layered carbonate and silica encrust fault fractures exposed in Trench 14 near Yucca Mountain, site of the proposed high-level nuclear waste repository in southern Nevada. Comparison of the stable carbon and oxygen isotopic compositions of the fracture carbonates with those of modern soil carbonates in the area shows that the fracture carbonates are pedogenic in origin and that they likely formed in the presence of vegetation and rainfall typical of a glacial climate. Their isotopic composition differs markedly from that of carbonate associated with nearby springs. The regional water table therefore remained below the level of Trench 14 during the time that the carbonates and silica precipitated, a period probably covering parts of at least the last 300,000 years. PMID:17818282

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

    International Nuclear Information System (INIS)

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

  5. Carbon-14 in lunar soil and in meteorites

    Science.gov (United States)

    Fireman, E. L.

    1978-01-01

    C-14 was measured in grain-size fractions of lunar soil 10084 and in samples of the Bruderheim chondrite and of several meteorites recently found in Antarctica (Allan Hills no. 5, 6, and 8). Temperature-release patterns were investigated. It was found that C-14 is released at temperatures below melting from small soil grains (less than 74 microns), but not from meteorites or from large soil grains. Below-melting C-14 contents increase with decreasing grain size in a manner similar to solar-wind-implanted rare-gas isotope contents (Eberhardt et al., 1970), whereas the C-14 released above melting temperatures is independent of grain size, suggesting that below-melting C-14 is solar-wind-implanted and above-melting C-14 is the result of cosmic ray spallations. The activity of C-14 in lunar samples is half that measured in the Bruderheim meteorite, which fell on May 4, 1970. No C-14 activity was observed in the Allan Hills chondrites; the C-14 limits suggest that these meteorites fell more than 25,000 years ago.

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

    Science.gov (United States)

    Almarri, Masoud S.

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

  7. Radiocarbon 14C differentiation of sparkling and carbonated wines

    International Nuclear Information System (INIS)

    Specific 14C-activities, percent of modern 14C-activity, and calculated percent of fermentation CO2 are presented for CO2 contained in commercial sparkling wines, labeled as champagne or produced by the bulk (charmat) process. These data are given for the production years 1976-1982. The survey encompassed effervescent wines produced in Spain, Italy, West Germany, California, and New York. Addition of synthetic CO2 to approximately 40 samples represented as sparkling wines was indicated by low 14C-activities of CO2 in these wines. Data for 14C-activity were also presented for the ethanol distilled from sparkling wines for the years 1977-1980. In all cases, the 14C-activity of ethanol was appropriate to the year of vintage

  8. Synthesis of the monosodium salt of carbon-14 labeled paclitaxel (Taxol) 2`-ethyl carbonate 7-phosphonooxymethyl ether, a potential prodrug of paclitaxel

    Energy Technology Data Exchange (ETDEWEB)

    Dischino, D.D.; Shuhui Chen; Golik, Jerzy; Walker, D.W.; Wong, H.S.L. [Bristol-Myers Squibb Co., Richard L. Gelb Center for Research and Development, Wallingford, CT (United States)

    1997-02-01

    The monosodium salt of carbon-14 labeled paclitaxel (Taxol) [N3`-{sup 14}COPh] 2`-ethyl carbonate 7-phosphonooymethyl ether, was prepared from C-14 labeled paclitaxel [N3`-{sup 14}COPh] in 5 steps. The radiochemical purity of the final product was greater than 99% and the specific activity was 25 {mu}Ci/mg. (author).

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

    Institute of Scientific and Technical Information of China (English)

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

    2004-01-01

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

  10. Synthesis of δ-aminolevulic acid. Application to the introduction of carbon-14 and of tritium

    International Nuclear Information System (INIS)

    Several new syntheses of δ aminolevulic acid (δ A.L.A.) have been studied. 14C-4 δ - aminolevulic acid has been obtained from 14C allylacetic carboxylic acid with a yield of 30 per cent with respect to barium carbonate and with a specific activity of 32 mCi/mM. The 14C-1 or 14C-2 δ-A.L.A. has been prepared from the 14C-1 or 14C-2 acetate with a yield of 55 per cent with respect to the acetate. Finally the tritiated δ-A.L.A. has been obtained for the first time by tritiation of ethyl phthalimidodehydrolevulate. (author)

  11. Tracing terrestrial carbon: a novel application of ∆14C in a humic lake

    Science.gov (United States)

    Keaveney, Evelyn; Reimer, Paula J.; Foy, Robert H.

    2016-04-01

    Lakes play an important yet underrated role in global carbon cycles. Terrestrial carbon (C) is buried and/or remineralised in significant quantities, and lake function may also be affected by catchment inputs with potential feedbacks for regional and global C cycling. Changing deposition chemistry, land use and climate induced impacts on hydrology will affect soil biogeochemistry, terrestrial C export, and hence lake ecology. Autochthonous production in lakes is based on dissolved inorganic C (DIC). DIC in alkaline lakes is partially derived from weathering of carbonaceous bedrock, a proportion of which is 14C-free. The low 14C activity yields an artificial age offset leading samples to appear hundreds to thousands of years older than their actual age. Dissolved organic carbon (DOC) and particulate organic carbon (POC) can contain terrestrial inputs. The terrestrial inputs can be labile or detrital and their age depends to a first order on their depth in catchment soil/peat stocks. We present a pilot study that uses the radiocarbon (∆14C) method to determine the source of carbon buried in the surface sediment of Lower Lough Erne, a humic, alkaline lake in northwest Ireland. ∆14C, δ13C and δ15N values were measured from phytoplankton and other biota, dissolved inorganic, dissolved organic and particulate organic carbon. A novel radiocarbon method, Stepped Combustion1 was used to estimate the degree of the burial of terrestrial carbon in surface sediment, collected in 2011. The ∆14C values of the low temperature fractions were comparable to algal ∆14C, while the high temperature fractions were 14C-depleted (older than bulk sediment). The ∆14C end-member model indicated that ~64% of carbon in surface sediment was derived from detrital terrestrial carbon. The same proportion of detrital/labile carbon was found in surface sediment of Upper Lough Erne in 2014, despite the differences in lake type and collection date. The use of ∆14C in conjunction with

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

    International Nuclear Information System (INIS)

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

  13. Determination of tritium and carbon-14 in accelerator waste

    Energy Technology Data Exchange (ETDEWEB)

    Argentini, M.; Weinreich, R. [Lab. of Radio- and Environmental Chemistry, Paul Scherrer Inst., Villigen-PSI (Switzerland)

    2003-07-01

    In dismounted parts of the accelerator facilities of paul scherrer institute, tritium and {sup 14}C were determined by low-level counting after chemical separation. In graphite targets used for the production of {pi}-mesons, tritium amounts from 1.7.10{sup 8} to 6.10{sup 8} Bq/g were found; the corresponding {sup 14}C data were 6 and 9 Ci/g, respectively. In the dismantled copper beam dump of Target E, the tritium content extended up to 2.8.10{sup 6} Bq/g, but no {sup 14}C could be detected. In mechanical parts of the beam dump, consisting of iron and stainless steel, respectively, the tritium amount ranged up to 5.3.10{sup 3} Bq/g, the {sup 14}C amount from 1 to 800 Bq/g. The separation procedures are described in detail. (orig.)

  14. Asphalt in carbon-14-dated archaeological samples from Terqa, Syria

    International Nuclear Information System (INIS)

    The results are reported of an organic geochemical study to verify contamination in 14C dated archaeological samples, which could account for much older apparent ages than expected. The data indicate that ancient asphalt must be the source of contamination, showing that caution should be exercised, in interpreting 14C dates of archaeological samples from areas containing asphalt or other fossil fuel deposits. (U.K.)

  15. Results of interagency effort to determine carbon-14 source term in low-level radioactive waste

    International Nuclear Information System (INIS)

    A preliminary estimate of the risks from the shallow land disposal of low-level radioactive wastes by EPA in 1984-1985 indicated that Carbon-14 caused virtually all of the risk and that these risks were relatively high. Therefore, an informal interagency group, which included the US Department of Energy, US Geological Survey, US Nuclear Regulatory Commission, and US Environmental Protection Agency, formed in 1985 to obtain up-to-date information on the activity and chemical form of Carbon-14 in the different types of LLW and how Carbon-14 behaves after disposal. The EPA acted as a focal point for collating the information collected by all of the Agencies and will publish a report in Fall 1986 on the results of the Carbon-14 data collection effort. Of particular importance, the study showed that Carbon-14 activity in LLW was overestimated approximately 2000%. This paper summarizes results of the Carbon-14 data collection effort. 40 references, 1 figure, 3 tables

  16. A larger pool of ozone-forming carbon compounds in urban atmospheres

    Energy Technology Data Exchange (ETDEWEB)

    Lewis, A.C.; Carslaw, N.; Marriott, P.J.; Kinghorn, R.M.; Morrison, P.; Lee, A.L.; Bartle, K.D.; Pilling, M.J.

    2000-06-15

    Volatile organic compounds play a central role in the processes that generate both urban photochemical smog and tropospheric ozone. For successful and accurate prediction of these pollution episodes, identification of the dominant reactive species within the volatile organic carbon pool is needed. At present, lack of resolution inherent in single-column chromatographic analysis limits such a detailed chemical characterization of the complex urban atmosphere. Here we present an improved method of peak deconvolution from double-column (orthogonal) gas chromatography. This has enabled us to isolate and classify more than 500 chemical species of volatile organic compounds in urban air, including over 100 multi-substituted monoaromatic and volatile oxygenated hydrocarbons. We suggest that previous assessments of reactive carbon species may therefore have underestimated the contribution made by volatile organic compounds to urban pollution, particularly for compounds with more that six carbon atoms. Incorporating these species in predictive models should greatly improve our understanding of photochemical ozone yields and the formation of harmful secondary organic aerosols. (author)

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

    Science.gov (United States)

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

    2006-10-01

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

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

    Science.gov (United States)

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

    2015-12-01

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

  19. Carbon 14 absorption and translocation in sugar cane

    International Nuclear Information System (INIS)

    Plant-cane stools were labelled with sup(14) CO sub(2), in the field, at Goiana-PE, Brazil, when 3, 7 and 11 months old. Each stool was enclosed in a chamber with sup(14) CO sub(2) for 90 minutes. The sub(14) C photosynthetic were measured in leaves, stalks, roots and soil 24 hours after labelling. Roots were divided into alive and dead and soil into rhizosphere and outer soil. At the end of the labelling period at 3, 7 and 11 months, 2, 19 and 1% of the initial sup(14) CO sub(2) were recovered in the plant and the soil. The low recovery of sub(14) C at 3 months could be attribute to losses by respiration and lack of sampling of the top growing point. The low CO sub(2) fixation and losses at first sampling in the 7 month old labelling were attributed to low light intensity during the day of labelling. Most of the recovered sub(14) C (>80%) was founded in the leaves but all plant parts received labelled photosynthetic. At 3 months, most of the sub(14) C translocated from the leaves went to the living roots (83%); at 7 and 11 months it went to the stalks (69 and 66%). While the roots received less than 2%. Root masses did not vary consistently along the plant cycle and dead root masses were always less than 10% of the total root mass. Radioactivity in the dead roots was always very low. These results suggest that the root system have a low turnover rate after 3 months old. (author)

  20. Atmospheric nuclear weapons test history narrated by carbon-14 in human teeth

    International Nuclear Information System (INIS)

    The atmospheric testing of nuclear weapons since 1945 caused a significant increase in the concentration of atmospheric 14C. The 14C concentration in plants that assimilate 14C directly by photosynthesis reflects the atmospheric 14C concentration. Carbon-14 is then transferred into the human body through the food chain. Based on animal experiments, the collagen in human teeth is metabolically inert after its formation. This implies that the collagen of each tooth retains the 14C concentration which reflects the 14C concentration in the blood at the time collagen metabolism ceased. The distribution of the 14C concentration in the collagen of teeth from subjects of various ages would follow a pattern similar to that shown by soft tissues. In this paper the authors elucidate the relationship between the number of nuclear weapon tests and the distribution of 14C concentration in teeth

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

    Science.gov (United States)

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

    2016-01-01

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

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

    Science.gov (United States)

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

    1952-07-08

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

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

    Science.gov (United States)

    Nakajima, K; Mitsuda, H

    1984-01-01

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

  4. Carbon-14 ages of Allan Hills meteorites and ice

    Science.gov (United States)

    Fireman, E. L.; Norris, T.

    1982-01-01

    Allan Hills is a blue ice region of approximately 100 sq km area in Antarctica where many meteorites have been found exposed on the ice. The terrestrial ages of the Allan Hills meteorites, which are obtained from their cosmogenic nuclide abundances are important time markers which can reflect the history of ice movement to the site. The principal purpose in studying the terrestrial ages of ALHA meteorites is to locate samples of ancient ice and analyze their trapped gas contents. Attention is given to the C-14 and Ar-39 terrestrial ages of ALHA meteorites, and C-14 ages and trapped gas compositions in ice samples. On the basis of the obtained C-14 terrestrial ages, and Cl-36 and Al-26 results reported by others, it is concluded that most ALHA meteorites fell between 20,000 and 200,000 years ago.

  5. Synthesis of carbon-14 labeled Taxol (paclitaxel). [Anticancer agent

    Energy Technology Data Exchange (ETDEWEB)

    Walker, D.G.; Swigor, J.E. (Bristol-Myers Squibb Co., Syracuse, NY (United States). Pharmaceutical Research Inst.); Kant, Joydeep; Schroeder, D.R. (Bristol-Myers Squibb Co., Wallingford, CT (United States). Pharmaceutical Research Inst.)

    1994-10-01

    Reductive cleavage of the C13 side chain of Taxol (1, paclitaxel) followed by regioselective silylation gave 7-triethylsilylbaccatin III (4). 3-O-Triethysilylation of 5 and subsequent reaction with benzoyl chloride-C7-[sup 14]C gave azetidinone 7. Coupling of 4 and 7 followed by deprotection gave 1.26 g of Taxol-N3'-[sup 14]C (11) having a specific activity of 26.5 mCi/mmol and a radiochemical purity of 95%. (author).

  6. Apparent Disequilibrium of Inorganic and Organic Carbon Compounds in Serpentinizing Fluids

    Science.gov (United States)

    Robinson, K.; Shock, E.

    2014-12-01

    During serpentinization of ultramafic rocks, ferrous iron in silicates is oxidized to ferric minerals and H2O is reduced to H2. This process is accompanied by the reduction of inorganic carbon, as observed in experiments and natural systems. To test the extent to which stable and metastable equilibria are reached among aqueous organic compounds during serpentinization, we sampled water and dissolved gases from circumneutral surface pools and hyperalkaline seeps in the Samail ophiolite in the Sultanate of Oman and analyzed for various carbon constituents, including dissolved inorganic carbon, dissolved organic carbon, methane, carbon monoxide, formate, acetate, and other small organic acid anions. Measurements of temperature, pH, dissolved H2, O2, major cations, major anions, and major and trace elements were also made. The aqueous composition of the analyzed samples was speciated based on ionic equilibrium interactions in order to obtain activities for inorganic carbon species, reduced carbon species, H2, and O2. The redox disequilibria among carbon species was then assessed using data and parameters for the revised HKF equations of state. This analysis demonstrates that the carbon species in this system are out of equilibrium with respect to one another in ways that cannot be compensated by altering the abundance of the other constituents within analytical uncertainties. Specifically, there is too much formate and too little methane relative to stable and metastable equilibria. This result implies the following: 1) Methane and formate equilibrated in separate parts of the system, given that no reasonable temperature, pressure, or composition changes satisfy equilibrium with their measured abundances. 2) Methane production is kinetically inhibited, as seen in experiments. 3) Microbial methane oxidation altered the abundance of methane and formate; methane oxidation to formate or carbonate is calculated to be extremely thermodynamically favorable in these fluids.

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

    Energy Technology Data Exchange (ETDEWEB)

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

    2004-07-01

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

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

    Science.gov (United States)

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

    2016-09-01

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

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

    Science.gov (United States)

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

    2016-02-01

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

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

    OpenAIRE

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

    2011-01-01

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

  11. Synthesis of carbon-14 labelled CD 271 (6-[3-(1-adamantyl)-4-methoxyphenyl]-2-naphthoic acid): a potential new agent for dermatology

    International Nuclear Information System (INIS)

    6-[3-(1-Adamantyl)-4-methoxyphenyl]-2-naphthoic acid, a promising new compound for the treatment of disorders of keratinization, has been synthesized in [14C]-labelled form from barium[14C]-carbonate via labelled benzene. Benzene-[U-14C] was converted to 4-bromo-methoxybenzene-[phenyl-U-14C] in six steps. Introduction of the adamantyl ring was carried out using 1-acetoxyadamantane under acid catalysis. 2-(1-Adamantyl)-4-bromo-methoxybenzene-[phenyl-U-14C] was converted to a zincate and coupled with methyl 6-bromo-2-naphthoate using a nickel catalyst. The product of the aryl coupling reaction was then saponified to give 6-[3-(1-adamantyl)-4-methoxyphenyl-[phenyl-U-14C

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

    Energy Technology Data Exchange (ETDEWEB)

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

    2013-03-01

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

  13. Displacement of carbon-14 labelled amino acids from leaves

    International Nuclear Information System (INIS)

    The displacement of amino acids from nature leaves was investigated. The amino acids (Ala, Asn, Asp, Glu, Gln, Val, Leu, Lys, Ser, Pro) were applied on the leaves in L-form, uniformly labelled with 14C, and the type and direction of displacement have been observed. Most of the studies have been carried out on bush beans aged 3 to 4 weeks. The experiments were carried out in climatic chambers; in one case, barley plants just reaching maturity were used. In order to find out whether the applied amino acids were also displaced in their original form, freeze-dried plants were extracted and the 14C activity of the various fraction was determined. The radioactivity of some free amino acids was determined after two-dimensional separation by thin film chromatography. (orig./HK)

  14. Determination of carbon-14 in environmental level, solid reference materials

    Energy Technology Data Exchange (ETDEWEB)

    Blowers, Paul, E-mail: paul.blowers@cefas.co.uk [Cefas Lowestoft Laboratory, Pakefield Road, Lowestoft, Suffolk, NR33 0HT (United Kingdom); Caborn, Jane, E-mail: jane.a.caborn@nnl.co.uk [NNL, Springfields, Salwick, Preston, Lancashire, PR4 0XJ (United Kingdom); Dell, Tony [Veterinary Laboratories Agency, New Haw, Addlestone, Surrey, KT15 3NB (United Kingdom); Gingell, Terry [DSTL, Radiation Protection Services, Crescent Road, Alverstoke, Gosport, Hants, PO12 2DL (United Kingdom); Harms, Arvic [National Physical Laboratory, Hampton Road, Teddington, Middlesex, TW11 0LW (United Kingdom); Long, Stephanie [Radiological Protection Institute of Ireland, 3 Clonskeagh Square, Clonskeagh Road, Dublin 14, Ireland (United Kingdom); Sleep, Darren [Centre for Ecology and Hydrology, Lancaster Environment Centre, Library Avenue, Bailrigg, Lancaster, LA1 4AP (United Kingdom); Stewart, Charlie [UKAEA (Waste Management Group), Chemical Support Services, D1310/14, Dounreay, Thurso, Caithness, KW14 7TZ (United Kingdom); Walker, Jill [Radiocarbon Dating, The Old Stables, East Lockinge, Wantage, Oxon OX12 8QY (United Kingdom); Warwick, Phil E. [GAU-Radioanalytical, National Oceanography Centre Southampton, European Way, Southampton, SO14 3ZH (United Kingdom)

    2011-10-15

    An intercomparison exercise to determine the {sup 14}C activity concentrations in a range of solid, environmental level materials was conducted between laboratories in the UK. IAEA reference materials, C2, C6 and C7, and an in-house laboratory QA material were dispatched in 2006 to ten laboratories comprising of members of the Analyst Informal Working Group (AIWG) and one other invited party. The laboratories performed the determinations using a number of techniques, and using the results each one was evaluated in terms of levels of precision, sensitivity and limits of detection. The results of the study show that all techniques are capable of successfully analysing {sup 14}C in environmental level materials, however, a shortage of certified environmental reference materials exists. The suitability of the IAEA reference materials and other material for use as reference materials was also assessed.

  15. Determination of carbon-14 in environmental level, solid reference materials

    International Nuclear Information System (INIS)

    An intercomparison exercise to determine the 14C activity concentrations in a range of solid, environmental level materials was conducted between laboratories in the UK. IAEA reference materials, C2, C6 and C7, and an in-house laboratory QA material were dispatched in 2006 to ten laboratories comprising of members of the Analyst Informal Working Group (AIWG) and one other invited party. The laboratories performed the determinations using a number of techniques, and using the results each one was evaluated in terms of levels of precision, sensitivity and limits of detection. The results of the study show that all techniques are capable of successfully analysing 14C in environmental level materials, however, a shortage of certified environmental reference materials exists. The suitability of the IAEA reference materials and other material for use as reference materials was also assessed.

  16. Biochemical Screening of Five Protein Kinases from Plasmodium falciparum against 14,000 Cell-Active Compounds.

    Directory of Open Access Journals (Sweden)

    Gregory J Crowther

    Full Text Available In 2010 the identities of thousands of anti-Plasmodium compounds were released publicly to facilitate malaria drug development. Understanding these compounds' mechanisms of action--i.e., the specific molecular targets by which they kill the parasite--would further facilitate the drug development process. Given that kinases are promising anti-malaria targets, we screened ~14,000 cell-active compounds for activity against five different protein kinases. Collections of cell-active compounds from GlaxoSmithKline (the ~13,000-compound Tres Cantos Antimalarial Set, or TCAMS, St. Jude Children's Research Hospital (260 compounds, and the Medicines for Malaria Venture (the 400-compound Malaria Box were screened in biochemical assays of Plasmodium falciparum calcium-dependent protein kinases 1 and 4 (CDPK1 and CDPK4, mitogen-associated protein kinase 2 (MAPK2/MAP2, protein kinase 6 (PK6, and protein kinase 7 (PK7. Novel potent inhibitors (IC50 < 1 μM were discovered for three of the kinases: CDPK1, CDPK4, and PK6. The PK6 inhibitors are the most potent yet discovered for this enzyme and deserve further scrutiny. Additionally, kinome-wide competition assays revealed a compound that inhibits CDPK4 with few effects on ~150 human kinases, and several related compounds that inhibit CDPK1 and CDPK4 yet have limited cytotoxicity to human (HepG2 cells. Our data suggest that inhibiting multiple Plasmodium kinase targets without harming human cells is challenging but feasible.

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

    Indian Academy of Sciences (India)

    Ram Seshadri

    2001-10-01

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

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

    International Nuclear Information System (INIS)

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

  19. Determination of Carbon-14 in environmental samples by mixing 14CO{sub 2} with a liquid scintillator; Determinacion de carbono-14 en muestras ambientales por incorporacion de 14CO{sub 2} a un centelleador liquido

    Energy Technology Data Exchange (ETDEWEB)

    Garcia, M. R.; Gomez, V.; Heras, M. C.; Beltran, M. A.

    1990-07-01

    A method for the determination of Carbon-14 (14CO2) in environmental samples has been developed. The method use the direct absorption of the carbon dioxide into Carbosorb, followed with incorporation of the mixture (Carbosorb-CO2) to the liquid scintillator. The results obtained to apply this method and the benzene synthesis, usual in our laboratory, are discussed and compared. The method of collection of atmospheric samples is also described. (Author) 10 refs.

  20. High molecule compound synthesis from carbon dioxide; Nisanka tanso karano kobunshi gosei

    Energy Technology Data Exchange (ETDEWEB)

    Mishima, K. [Fukuoka Univ., Fukuoka (Japan)

    2000-09-05

    Recently, synthesis of organic substances and high molecule compounds using carbon dioxide of liquid or supercritical state as raw material is paid attention so as the influential means to realize the green chemistry. A zinc based catalyst which could synthesize the activated copolymer from oxidized cyclohexane and carbon dioxide was developed by Coates, Beckman et al. The high-activated fluoridation zinc based catalyst which dissolved the high-pressure carbon dioxide was developed by Beckman, etc. The possibility of the manufacturing of the high molecule copolymer which is made from carbon dioxide and oxidized cyclohexane as a raw material was shown by an appearance of this catalyst. In addition, a synthesizing method of lactone from carbon dioxide and olefinic hydrocarbon is being examined by Beckman. If this method is used practically, the manufacturing of a gentle biodegradable polymer in the environment which is made from carbon dioxide as a raw material becomes also possible. However, adequate catalysts are necessary so that this reaction may progress. (NEDO)

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

    Science.gov (United States)

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

    2015-12-15

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

  2. Characteristics of 14C and 13C of carbonate aerosols in dust storm events in China

    Science.gov (United States)

    Chen, Bing; Jie, Dongmei; Shi, Meinan; Gao, Pan; Shen, Zhenxing; Uchida, Masao; Zhou, Liping; Liu, Kexin; Hu, Ke; Kitagawa, Hiroyuki

    2015-10-01

    In contrast with its decrease in western China deserts, the dust storm event in eastern China, Korea, and Japan shows an increase in frequency. Although the drylands in northeastern China have been recognized as an important dust source, the relative contributions of dust transport from the drylands and deserts are inconclusive, thus the quantification of dust storm sources in downwind area remains a challenge. We measured the 14C and 13C contents in carbonates of dust samples from six sites in China, which were collected for the duration of dust storm events in drylands, deserts, and urban areas. The δ13C of the dryland dust samples considerably varied in a range of - 9.7 to - 5.0‰, which partly overlapped the desert dust carbonate δ13C ranges. The 14C content of the dryland dust carbonates showed a narrow range of 60.9 ± 4.0 (as an average and 1 SD of five samples) percent modern carbon (pMC), indicating the enrichment of modern carbonate. Dust samples in desert regions contained relatively aged carbonates with the depleting 14C showing of 28.8 ± 3.3 pMC. After the long-range transport of the western China desert dust plume, the carbonates collected at the southern China remained the depletion of 14C (33.5 ± 5.3 pMC) as in the desert regions. On the other hand, the samples of dust storm events at the urban areas of eastern China showed an enrichment of 14C contents (46.2 ± 5.0 pMC, n = 7), which might be explained by the stronger contribution of modern-carbonate-rich dryland dust.

  3. Two dimensional model study of atmospheric transport using carbon-14 and strontium-90 as inert tracers

    International Nuclear Information System (INIS)

    This study tests the transport processes in the LLNL two-dimensional chemical-radiative-transport model using recently reanalyzed carbon-14 and strontium-90 data. These radioactive tracers were produced bythe atmospheric nuclear bomb tests of 1952--58 and 1961--62, and they were measured at a few latitudes up to 35 kilometers over the period 1955--1970. Selected horizontal and vertical eddy diffusion coefficients were varied in the model to test their sensitivity to short and long term transpose of carbon-14. A sharp transition of Kzz and Kyy through the tropopause, as opposed to a slow transition between the same limiting values, shows a distinct improvement in the calculated carbon-14 distributions, a distinct improvement in the calculated seasonal and latitudinal distribution of ozone columns (relative to TOMS observations), and a very large difference in the calculated ozone reduction by a possible fleet of High Speed Civil Transports. Calculated northern hemisphere carbon-14 is more sensitive to variation of Kyy than are global ozone columns. Strontium-90 was used to test the LLNL tropopause height at four different latitudes. Starting with the 1960 background distribution of carbon-14, we calculate the input of carbon-14 as the sum of each nuclear test of the 1961--62 series, using two bomb-cloud rise models. With the Seitz bomb-rise formulation in the LLNL model, we find good agreement between calculated and observedcarbon-14 (with noticeable exceptions at the north polar tropopause and the short-term mid-latitude mid-stratosphere) between 1963 and 1970

  4. Characteristics study of a system for carbon 14 dating

    International Nuclear Information System (INIS)

    The developing of a radiocarbon dating laboratory, specially built to deal with carbonate samples from underground water, at the Institute de Energia Atomica, required the optimization of a benzene synthetizer, and also of the operative conditions of the liquid scintillator counter, used in sample measurements. An average yield of about 70% was obtained in our benzenic synthesis. If more refined conditions were used, better results could have been obtained, but the reported yield is good enough for our necessities. A comparison of the ages of several shell samples was done between the Geochronology Laboratory, belonging to the Instituto de Geociencias, at Sao Paulo University and our dating laboratory. The agreement between the results was fairly good, according to the precision required

  5. A synthetic approach to carbon-14 labeled anti-bacterial naphthyridine and quinolone carboxylic acids

    Energy Technology Data Exchange (ETDEWEB)

    Ekhato, I.V.; Huang, C.C. (Parke, Davis and Co., Ann Arbor, MI (United States))

    1993-09-01

    Labeled versions of (S)-clinafloxacin (1) and two napththyridine carboxylic acid anti-bacterial compounds 2 and 3 which are currently in development were synthesized. Preparations started from hitherto unknown bromo compounds 22 and 10, from which the corresponding [sup 14]C-labeled aromatic carboxylic acids 23 and 12 were generated by metal-halogen exchange followed by carboxylation reaction. Details of these preparations are given. (author).

  6. Carbon-14 transfer into rice plants from a continuous atmospheric source: observations and model predictions

    International Nuclear Information System (INIS)

    Carbon-14 (14C) is one of the most important radionuclides from the perspective of dose estimation due to the nuclear fuel cycle. Ten years of monitoring data on 14C in airborne emissions, in atmospheric CO2 and in rice grain collected around the Tokai reprocessing plant (TRP) showed an insignificant radiological effect of the TRP-derived 14C on the public, but suggested a minor contribution of the TRP-derived 14C to atmospheric 14C concentrations, and an influence on 14C concentrations in rice grain at harvest. This paper also summarizes a modelling exercise (the so-called rice scenario of the IAEA's EMRAS program) in which 14C concentrations in air and rice predicted with various models using information on 14C discharge rates, meteorological conditions and so on were compared with observed concentrations. The modelling results showed that simple Gaussian plume models with different assumptions predict monthly averaged 14C concentrations in air well, even for near-field receptors, and also that specific activity and dynamic models were equally good for the prediction of inter-annual changes in 14C concentrations in rice grain. The scenario, however, offered little opportunity for comparing the predictive capabilities of these two types of models because the scenario involved a near-chronic release to the atmosphere. A scenario based on an episodic release and short-term, time-dependent observations is needed to establish the overall confidence in the predictions of environmental 14C models

  7. Stability, defect and electronic properties of graphane-like carbon-halogen compounds

    Institute of Scientific and Technical Information of China (English)

    Lu Di; Yang Yu-Rong; Xiao Yang; Zhang Xiao-Yu

    2011-01-01

    We perform first-principles total energy calculations to investigate the stabilities and the electronic structures of graphane-like structures of carbon-halogen compounds,where the hydrogen atoms in the graphane are substituted by halogen atoms.Three halogen elements,fluorine (F),chlorine (Cl) and bromine (Br),are considered,and the graphanelike structures are named as CF,CCl and CBr,respectively.It is found that for the single-atom adsorption,only the F adatom can be chemically adsorbed on the graphene.However,the stable graphane-like structures of CF,CCl and CBr can form due to the interaction between the halogen atoms.The carbon atoms in the stable CF,CCl and CBr compounds are in the sp3 hybridization,forming a hexagonal network similar to the graphane.The electronic band calculations show that CF and CCl are semiconductors with band gaps of 3.28 eV and 1.66 eV,respectively,while CBr is a metal.Moreover,the molecular dynamics simulation is employed to clarify the stabilities of CF and CCl.Those two compounds are stable at room temperature.A high temperature (≥ 1200 K) is needed to damage CF,while CCl is destroyed at 700 K.Furthermore,the effects of a vacancy on the structure and the electronic property of CF are discussed.

  8. Sorption of DOM and hydrophobic organic compounds onto sewage-based activated carbon.

    Science.gov (United States)

    Björklund, Karin; Li, Loretta Y

    2016-01-01

    Treatment of stormwater via sorption has the potential to remove both colloidal and dissolved pollutants. Previous research shows that activated carbon produced from sewage sludge is very efficient in sorbing hydrophobic organic compounds (HOCs), frequently detected in stormwater. The aim of this research was to determine whether the presence of dissolved organic matter (DOM) has a negative effect on the adsorption of HOCs onto sludge-based activated carbon (SBAC) in batch adsorption tests. Batch adsorption tests were used to investigate the influence of two types of DOM - soil organic matter and humic acid (HA) technical standard - on the sorption of HOCs onto SBAC, and whether preloading adsorbent and adsorbates with DOM affects HOC sorption. The results indicate that soil DOM and HAs do not have a significant negative effect on the adsorption of HOCs under tested experimental conditions, except for a highly hydrophobic compound. In addition, preloading SBAC or HOCs with DOM did not lead to lower adsorption of HOCs. Batch adsorption tests appear to be inefficient for investigating DOM effects on HOC adsorption, as saturating the carbon is difficult because of high SBAC adsorption capacity and low HOC solubility, so that limited competition occurs on the sorbent. PMID:27533860

  9. Phase relation of LaFe11.6Si1.4 compounds annealed at different high-temperature and the magnetic property of LaFe11.6−CoSi1.4 compounds

    Indian Academy of Sciences (India)

    Xiang Chen; Yungui Chen; Yongbai Tang

    2012-04-01

    LaFe11.6Si1.4 compounds are annealed at different high temperatures from 1323 to 1623 K. The powder X-ray diffraction patterns show that large amount of NaZn13-type phase begins to be observed in LaFe11.6Si1.4 compound after being annealed at 1423 K for 5 h. In the temperature range from 1423 to 1523 K, the -Fe and LaFeSi phases rapidly decrease to form 1:13 phase. LaFeSi phase is rarely observed in the XRD pattern in the LaFe11.6Si1.4 compound annealed at 1523 K (5 h).With annealing temperature increasing to 1573 K and 1673 K, La5Si3 phase is detected, and there is a certain amount of LaFeSi phase when the annealing temperature is 1673 K. The amount of impurity phases in the LaFe11.6Si1.4 compound annealed by the two-stage annealing consisting of high temperature (>1523 K) and 1523 K is larger than that of the single stage annealing at 1523 K under the same time. According to the results of different high-temperature annealing, LaFe11.6−CoSi1.4 (0.1 ≤ ≤ 0.8) compounds are annealed at 1523 K (5 h). The main phase is NaZn13-type phase, and the impurity phase is a small amount of -Fe in LaFe11.6−CoSi1.4 compounds. With increase in Co content from = 0.1 to 0.8, the Curie temperature C, goes up from 207 to 285 K. The introduction of Co element weakens the itinerant electron metamagnetic transition, and also results in the change of magnetic transition type from first to second order at about = 0.5. The magnetic entropy change decreases from 19.94 to 4.57 J /kg K with increasing Co concentration at a low magnetic field of 0–2 T. But the magnetic hysteresis loss around C reduces remarkably from 26.2 J /kg for = 0.1 to 0 J /kg for = 0.8.

  10. Sampling and monitoring of carbon-14 in gaseous effluents from nuclear facilities

    International Nuclear Information System (INIS)

    This study reviews the possibilities from sampling and monitoring C-14 in gaseous effluents from nuclear facilities. After oxidation of various forms of carbon-14 in the off-gas into CO2 three main processes for trapping are used either separately or in combination. These are sorption, freezing and chemical processes. Absorption in alkaline solutions or solids or molecular sieve adsorption are the most frequently used methods. The main counting methods used are gas proportional counting and liquid scintillation counting

  11. Carbon-14 production compared to oxygen isotope records from Camp Century, Greenland and Devon Island, Canada

    International Nuclear Information System (INIS)

    Carbon-14 production rate variations that are not explainable by geomagnetic changes are thought to be in antiphase with solar activity and as such should be in antiphase with paleotemperature records or proxy temperature histories such as those obtainable from oxygen isotope analyses of ice cores. Oxygen isotope records from Camp Century, Greeland and Devon Island Ice Cap are in phase with each other over thousands of years and in antiphase to the 14C production rate residuals. (Auth.)

  12. Proportion of biogenic carbon in flue gas by carbon-14 measurement; Biohiili2: Biohiilen mittaus savukaasusta hiili-14-menetelmaellae

    Energy Technology Data Exchange (ETDEWEB)

    Lehtomaeki, J.; Antson, O.; Hongisto, M.; Knuuttila, M.; Roine, J.; Raesaenen, J.; Tormonen, K. [VTT Technical Research Centre of Finland, Espoo (Finland); Jungner, H. [Helsinki Univ. (Finland)

    2007-07-01

    The subject of this project is closely related to EU's emissions trading system and to the current and future monitoring needs therein. The determination of fossil part of emissions originated from various fuels by stack measurements or by laboratory analyses could possibly find users also in other fields outside the ETS (e.g. waste incineration). After the market analysis and preliminary measurements carried out in the previous Biocarbon project this project focused on the development of the sampling method for stack measurements and to the validation of isotope measurements. The results obtained for fossil proportion of the fuel by current methods will be compared to those obtained by isotope measurements. The operation of the sampling system was tested in long period tests in plant conditions. Moreover, the sample preparation methods and isotope measurements were validated by measuring the proportions of biogenic and fossil carbon of known traffic fuel mixtures. The developed service concept can also be utilised as a fraud prevention measure related to the expanding international biofuels-trade. (orig.)

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

    Science.gov (United States)

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

    2016-07-01

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

  14. The fate of organic compounds in a cement-based repository: impact on the engineered barrier and the release of C-14 from the near field

    International Nuclear Information System (INIS)

    The degradation of organic materials is taken into account in the safety analysis for a L/ILW (Low- and intermediate-level radioactive waste) repository in Switzerland with the aim of assessing possible impacts on the cement barrier. The waste forms to be disposed of in the planned L/ILW repository will contain HMW polymers and LMW monomeric organic materials. It is anticipated that these organic materials have different degradation rates and therefore different life times in a repository. While the decomposition of LMW organics is expected to be fast and complete during the oxic and early anoxic states of a repository, i.e. before and shortly after repository closure, the decomposition of the HMW polymeric materials is expected to be very slow and, for some materials, to occur over the entire life time of the repository. The degradation of organic materials generates CO2 which gives rise to carbonation of the cement barrier. The maximum acceptable loading of organics in the near field with no detrimental effect on radionuclide immobilization can be estimated on the assumption that at maximum 2/3 of the total portlandite inventory of hydrated cement is allowed to convert to CaCO3 in the case of waste compartments for which the cementitious barrier should remain intact. The maximum loading is determined by the inventory of the organic material under consideration as well as the carbon content and the oxidation state of carbon of the material. Carbon-14 bound in organic compounds is considered to be an important contributor to the annual dose released from a L/ILW repository. While the 14C inventory is well known, the chemical speciation of 14C in the cementitious near field upon liberation in the course of the corrosion of activated steel is only poorly understood. Preliminary corrosion tests with non-activated steel powders show the formation of gaseous and dissolved organic carbon species, e.g. alkanes/alkenes, alcohols, aldehydes, and carboxylic acids, containing

  15. Design, Synthesis and Biological Evaluation of 1,4-Disubstituted-3,4-dihydroisoquinoline Compounds as New Tubulin Polymerization Inhibitors

    Directory of Open Access Journals (Sweden)

    Ling Zhang

    2015-05-01

    Full Text Available A series of 1,4-disubstituted-3,4-dihydroisoquinoline derivatives designed as tubulin polymerization inhibitors were synthesized. Their cytotoxic activities against the CEM leukemia cell line were evaluated. Most of them displayed moderate cytotoxic activities, and compounds 21 and 32 showed good activities with IC50 of 4.10 and 0.64 μM, respectively. The most potent compound 32 was further confirmed to be able to inhibit tubulin polymerization, and its hypothetical binding mode with tubulin was obtained by molecular docking.

  16. 14.7% efficient mesoscopic perovskite solar cells using single walled carbon nanotubes/carbon composite counter electrodes

    Science.gov (United States)

    Li, Hao; Cao, Kun; Cui, Jin; Liu, Shuangshuang; Qiao, Xianfeng; Shen, Yan; Wang, Mingkui

    2016-03-01

    A single walled carbon nanotube (SWCNT) possesses excellent hole conductivity. This work communicates an investigation of perovskite solar cells using a mesoscopic TiO2/Al2O3 structure as a framework in combination with a certain amount of SWCNT-doped graphite/carbon black counter electrode material. The CH3NH3PbI3-based device achieves a power conversion efficiency of 14.7% under AM 1.5G illumination. Detailed investigations show an increased charge collection in this device compared to that without the SWCNT additive.A single walled carbon nanotube (SWCNT) possesses excellent hole conductivity. This work communicates an investigation of perovskite solar cells using a mesoscopic TiO2/Al2O3 structure as a framework in combination with a certain amount of SWCNT-doped graphite/carbon black counter electrode material. The CH3NH3PbI3-based device achieves a power conversion efficiency of 14.7% under AM 1.5G illumination. Detailed investigations show an increased charge collection in this device compared to that without the SWCNT additive. Electronic supplementary information (ESI) available. See DOI: 10.1039/c5nr07347b

  17. 75 FR 40729 - Residues of Quaternary Ammonium Compounds, N-Alkyl (C12-14

    Science.gov (United States)

    2010-07-14

    ...) 305-5805. II. Summary of Petitioned-For Exemption In the Federal Register of November 28, 2007 (72 FR... represents the different number of hydrocarbon carbon moieties delineated by different percentages (e.g... chemicals together because variance in the length and conformation of alkyl carbon chains between 12 and...

  18. A Brief Review of the Application of 14C in Terrestrial Carbon Cycle Studies

    Energy Technology Data Exchange (ETDEWEB)

    Guilderson, T; Mcfarlane, K

    2009-10-22

    An over-arching goal of the DOE TCP program is to understand the mechanistic controls over the fate, transport, and residence time of carbon in the terrestrial biosphere. Many of the modern process and modeling studies focus on seasonal to interannual variability. However, much of the carbon on the landscape and in soils is in separate reservoirs with turnover times that are multi-decadal to millennial. It is the controls on these longer term pools or reservoirs that is a critical unknown in the face of rising GHGs and climate change and uncertainties of the terrestrial biosphere as a future global sink or source of atmospheric CO{sub 2} [eg., Friedlingstein et al., 2006; Govindasamy et al., 2005; Thompson et al., 2004]. Radiocarbon measurements, in combination with other data, can provide insight into, and constraints on, terrestrial carbon cycling. Radiocarbon (t{sub 1/2} 5730yrs) is produced naturally in the stratosphere when secondary neutrons generated by cosmic rays collide with {sup 14}N atoms [Libby 1946; Arnold and Libby, 1949]. Upon formation, {sup 14}C is rapidly oxidized to CO and then to CO{sub 2}, and is incorporated into the carbon cycle. Due to anthropogenic activities, the amount of {sup 14}C in the atmosphere doubled in the mid/late 1950s and early 1960s from its preindustrial value of {sup 14}C/{sup 12}C ratio of 1.18 x 10{sup -12} [eg., Nydal and Lovseth, 1983]. Following the atmospheric weapons test ban in 1963, the {sup 14}C/{sup 12}C ratio, has decreased due to the net isotopic exchange between the ocean and terrestrial biosphere [eg., Levin and Hessheimer, 2000] and a dilution effect due to the burning of {sup 14}C-free fossil fuel carbon, the 'Suess Effect' [Suess, 1955]. In the carbon cycle literature, radiocarbon measurements are generally reported as {Delta}{sup 14}C, which includes a correction for mass dependent fractionation [Stuiver and Polach, 1977]. In the context of carbon cycle studies radiocarbon measurements can be

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

    CERN Document Server

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

    2014-01-01

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

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

    Energy Technology Data Exchange (ETDEWEB)

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

    2012-07-30

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

  1. Variation of 14C, 137Cs and stable carbon composition in forest soil and its implications

    International Nuclear Information System (INIS)

    In Japan, about 70% of land area is covered by forest. Therefore, forest ecosystem plays a vital role in ultimate fate of radionuclides and carbon cycle in terrestrial environment. Three undisturbed forest soil profiles were collected from Ibaraki Prefecture, Japan. The 137Cs data illustrate that maximum fallout deposition of 137Cs took place around 1964. 14C determination shows that 14C also has peak values in the top 10 cm of the soil profiles ascribed to the highest bomb 14C level in 1960's. The 13C data show that the turnover dynamics of soil organic carbon could be described very well by progressive enrichment values of δ13C. (author)

  2. Preparation of 14C-Labeled Multi-walled Carbon Nano-tubes for Biodistribution Investigations

    International Nuclear Information System (INIS)

    A new method allowing the 14C-labeling of carboxylic acid functions of carbon nano-tubes is described. The key step of the labeling process is a de-carbonylation reaction that has been developed and optimized with the help of a screening method. The optimized process has been successfully applied to multi-walled carbon nano-tubes (MWNTs), and the corresponding 14C-labeled nano-tubes were used to investigate their in vivo behavior. Preliminary results obtained after i.v. contamination of rats revealed liver as the main target organ. Radiolabeling of NTs with a long-life radioactive nucleus like 14C, coupled to a highly sensitive autoradiographic method, that provides a unique detection threshold, will make it possible to determine for a long time period whether or not NTs remain in any organs after animal exposure. (authors)

  3. Photosynthesis and assimilate partitioning characteristics of the coconut palm as observed by carbon-14 labelling

    International Nuclear Information System (INIS)

    A technique was developed on the use of carbon dioxide(carbon-14 labelled) rapid labelling of foliage and to ascertain photosynthesis and partitioning characteristics of labelled assimilate into other parts of the coconut palm. An eight-year-old Tall x Tall young coconut palm growing under field conditions at Bandirippuwa Estate and with six developing bunches , was selected for this study. The labelling was carried out on a bright sunny day and soil was at field capacity. Seventh leaf from the youngest open leaf was used for labelling with 5 mCi of sodium bi carbonate (Carbon-14 labelled). The results revealed that within 24 hours, 60% of the labelled assimilate was partitioned into other parts of the palm and at the end of the seventh day about 18% of the labelled assimilate still remained in the labelled leaf. Among the developing bunches fifth and sixth bunches from the youngest developing bunch received more labelled assimilate than young developing bunches above them. It was revealed that partitioning of assimilate into various ''sinks'' is determined by the developmental stage or activeness of the ''sink''. The proportion of C-14 labelled carbon assimilate, partitioned into developing bunches was substantially low compared to the total amount of labelled carbon fixed by the labelled leaf. Further, it was observed that partitioning of assimilated labelled carbon into the young leaves above, as well as the mature leaves below the labelled leaf. The complex vascular anatomy of the palms could be attributed to this pattern of partitioning of assimilates into upper and lower leaves from the labelled leaf

  4. Stable carbon and hydrogen isotopic fractionations of alkane compounds and crude oil during aerobically microbial degradation

    Institute of Scientific and Technical Information of China (English)

    PENG Xianzhi; ZHANG Gan; CHEN Fanzhong; LIU Guoqing

    2004-01-01

    Normal alkane compounds dodecane, pentadecane, hexadecane, octadecane, tetracosane, isoprenoid alkane pristane and a crude oil sample were aerobically biodegraded with a pure bacterial strain GIM2.5 and white rot fungus Phanerochaete Chrysosporium-1767 to monitor the kinetic fractionation of the molecular stable carbon (δ13C) and hydrogen (δD) isotopes in the course of biodegradation. Both δ13C (V-PDB) and δ D (V-SMOW) remained stable for the standard alkane compounds and n-alkane components (from n-C13 to n-C25) of the crude oil, generally varying in the range of ±0.5‰ and ±5‰ respectively, within the range of the instrumental precisions, especially for those molecularly heavier than n-C16 during microbial degradation. These results indicate that molecular stable carbon and hydrogen isotopic fingerprints can be promising indicators for tracing the sources of petroleum-related contaminants in the environment, especially in the case of severe weathering when they are difficult to be unambiguously identified by the chemical fingerprints alone.

  5. Transport and biotransformation of organic carbon and nitrate compounds in unsaturated soil conditions.

    Science.gov (United States)

    Bunsri, Thidarat; Sivakumar, Muttucumaru; Hagare, Dharmappa

    2008-01-01

    The lack of drinking water was one of the hot environmental issues that focused on the contaminants released from the failure of sanitary systems. Organic carbon and nitrate compounds were concerned since they represented a potential risk to human health and environment. Mathematical modelling was an effective tool for understanding and estimating the fate and transport of contaminants. An organic carbon and nitrate compounds transport model was developed using the mass balance concept. Richards and multiplicative Monod equations supported the estimating of advection-dispersion transport and biodegradation processes, respectively. The numerical solutions were obtained using the MATLAB programme. The model capability was evaluated using pilot scale experimental data. The depth-averaged time series of pressure head and contaminants concentration profiles were measured several times a week during 91 days. Simulations were found to provide reasonable agreement with the observed data. The aerobic biodegradation zone was observed within 15 cm depth of soil column. Even though the column was operated for 91 days, soil microbes were enough to retard these contaminants. This confirmed that the developed model could be applied to simulate the transport of the contaminants under real time boundary conditions. PMID:19092190

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

    Science.gov (United States)

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

    2015-08-01

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

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

    International Nuclear Information System (INIS)

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

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

    Directory of Open Access Journals (Sweden)

    Penwisa Pisitsak

    2012-01-01

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

  9. Factors affecting carbon-14 activity of unsaturated zone CO2 and implications for groundwater dating

    Science.gov (United States)

    Wood, Cameron; Cook, Peter G.; Harrington, Glenn A.; Meredith, Karina; Kipfer, Rolf

    2014-11-01

    Unsaturated zone processes may influence the carbon-14 (14C) activity of infiltrating groundwater and thus introduce error in derived groundwater residence times. However unsaturated zone 14C activities are rarely measured and there is little understanding of how they may vary spatially in a groundwater basin. In this study we measured 14C activity in unsaturated zone gas at five sites with different watertable depths (8.2-31.5 m) in the arid Ti Tree Basin, central Australia. We observed a relatively uniform decrease in 14C activity of unsaturated zone gas with depth at most sites, with variation in unsaturated zone depths leading to variation in 14C activities directly above the watertable at each site (ranging from 54 to 106 percent Modern Carbon (pMC)). Through modelling we show that the profiles are influenced by CO2 production at different depths from sources with different isotopic ratios, including production of ‘modern' CO2 in the root zone and production of ‘old' CO2 above the watertable. Scenario modelling showed that these processes are independent of recharge when recharge is low (0-10 mm y-1) but that higher recharge rates (>100 mm y-1) result in more advective transport of atmospheric CO2 to the watertable. The variation in 14C above the watertable was more sensitive to watertable depth and shallow and deep CO2 production rates. These findings offer insight into how unsaturated zone 14C activities may vary spatially and provide guidance as to when 14C depletion in unsaturated zone CO2 may become important for groundwater dating, particularly in arid settings.

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

    Science.gov (United States)

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

    2014-01-01

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

  11. Multiphase Carbon-14 Transport in a Near-Field-Scale Unsaturated Column of Natural Sediments

    Energy Technology Data Exchange (ETDEWEB)

    D. T. Fox; Mitchell A. Plummer; Larry C. Hull; D. Craig Cooper

    2004-03-01

    Wastes buried at the Subsurface Disposal Area (SDA) of the Idaho National Engineering and Environmental Laboratory include activated metals that release radioactive carbon-14 (14C) as they corrode. To better understand 14C phase partitioning and transport in the SDA sediments, we conducted a series of transport experiments using 14C (radio-labeled sodium carbonate) and nonreactive gas (sulfur hexafluoride) and aqueous (bromide and tritiated water) tracers in a large (2.6-m high by 0.9-m diameter) column of sediments similar to those used as cover material at the SDA. We established steady-state unsaturated flow prior to injecting tracers into the column. Tracer migration was monitored using pore-water and pore-gas samples taken from co-located suction lysimeters and gas ports inserted at ~0.3-m intervals along the column’s length. Measurements of 14C discharged from the sediment to the atmosphere (i.e., 14CO2 flux) indicate a positive correlation between CO2 partial pressure (pCO2) in the column and changes in 14CO2 flux. Though 14CO2 diffusion is expected to be independent of pCO2, changes of pCO2 affect pore water chemistry sufficiently to affect aqueous/gas phase 14C partitioning and consequently 14C2 flux. Pore-water and -gas 14C activity measurements provide an average aqueous/gas partitioning ratio, Kag, of 4.5 (±0.3). This value is consistent with that calculated using standard carbonate equilibrium expressions with measured pH, suggesting the ability to estimate Kag from carbonate equilibrium. One year after the 14C injection, the column was cored and solid-phase 14C activity was measured. The average aqueous/solid partition coefficient, Kd, (1.6 L kg-1) was consistent with those derived from small-scale and short-term batch and column experiments using SDA sediments, suggesting that bench-scale measurements are a valid means of estimating aqueous/solid partitioning at the much larger spatial scale considered in these meso-scale experiments. However

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

    Science.gov (United States)

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

    2012-10-01

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

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

    Science.gov (United States)

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

    2012-10-01

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

  14. Carbon-14 in waste packages for spent fuel in a tuff repository

    International Nuclear Information System (INIS)

    Carbon-14 is produced naturally by cosmic ray neutrons in the upper atmosphere. It is also produced in nuclear reactors, in amounts much smaller than the global inventory. About one-third of this is released directly to the atmosphere, and the other two-thirds remains in the spent fuel. Both the Environmental Protection Agency and the Nuclear Regulatory Commission have established limits on release of the 14C in spent fuel. This is of particular concern for the proposed repository in tuff, because of the unsaturated conditions and the consequent possibility of gaseous transport of 14C as CO2. Existing measurements and calculations of the 14C inventory in spent fuel are reviewed. The physical distribution and chemical forms of the 14C are discussed. Available data on the release of 14C from spent fuel in aqueous solutions and in gaseous environments of air, nitrogen, and helium are reviewed. Projected 14C behavior in a tuff repository is described. It is concluded that 14C release measurements from spent fuel into moist air at temperatures both above and below the in situ boiling point of water as well as detailed transport calculations for the tuff geological environment will be needed to determine whether the 10CFR60 and 40CFR191 requirements can be met. 56 refs., 1 tab

  15. Modelling the Environmental Transfer of Tritium and Carbon-14 to Biota and Man. Report of the Tritium and Carbon-14 Working Group of EMRAS Theme 1

    International Nuclear Information System (INIS)

    Hydrogen and carbon are biologically-regulated, essential elements that are highly mobile in the environment and the human body. As isotopes of these elements, tritium and 14C enter freely into water (in the case of tritium), plants, animals and humans. This complex behaviour means that there are substantial uncertainties in the predictions of models that calculate the transfer of tritium and 14C through the environment. The EMRAS Tritium/C14 Working Group (WG) was set up to establish the confidence that can be placed in the predictions of such models, to recommend improved modelling approaches, and to encourage experimental work leading to the development of data sets for model testing. The activities of the WG focused on the assessment of models for organically bound tritium (OBT) formation and translocation in plants and animals, the area where model uncertainties are largest. Environmental 14C models were also addressed because the dynamics of carbon and OBT are similar. The goals of the WG were achieved primarily through nine test scenarios in which model predictions were compared with observations obtained in laboratory or field studies. Seven of the scenarios involved tritium, covering terrestrial and aquatic ecosystems and steady-state and dynamic conditions. The remaining two scenarios concerned 14C, one addressing steady-state concentrations in plants and the other time-dependent concentrations in animals. The WG also considered one model intercomparison exercise involving the calculation of doses following a hypothetical, short-term release of tritium to the atmosphere in a farming area. Finally, the WG discussed the nature of OBT and proposed a definition to promote common understanding and usage within the international tritium community. The models used by the various participants varied in complexity from simple specific activity approaches to dynamic compartment models and process-oriented models, in which the various transfer processes were

  16. Activated Carbon Adsorption Characteristics of Multi-component Volatile Organic compounds in a Fixed Bed Adsorption Bed

    Energy Technology Data Exchange (ETDEWEB)

    Cho, Jong Hoon; Rhee, Young Woo [Chungnam National University, Daejeon (Korea, Republic of); Lee, Sihyun [Korea Institute of Energy Research, Daejeon (Korea, Republic of)

    2016-04-15

    This study aims to examine absorption characteristics of toluene, isopropyl alcohol (IPA), ethyl acetate (EA), and ternary-compounds, all of which are widely used in industrial processes, by means of four types of commercial activated carbon substances. It turned out that among the three types of volatile organic compounds, the breakthrough point of activated carbon and that of IPA, whose affinity was the lowest, were the lowest, and then that of EA and that of toluene in the order. With the breakthrough point of IPA, which was the shortest, as the standard, changes in the breakthrough points of unary-compounds, binary-compounds, and ternary-compounds were examined. As a result, it turned out that the larger the number of elements, the lower the breakthrough point. This resulted from competitive adsorption, that is, substitution of substances with a low level of affinity with those with a high level of affinity. Hence, the adsorption of toluene-IPA-EA and ternary-compounds require a design of the activated carbon bed based on the breakthrough of IPA, and in the design of activated carbon beds in actual industries as well, a substance whose level of affinity is the lowest needs to be the standard.

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

    Science.gov (United States)

    Dijkstra, Paul; van Groenigen, Kees-Jan

    2015-04-01

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

  18. Algal C-14 and total carbon metabolisms 2. Experimental observations with the diatom Skeletonema costatum

    DEFF Research Database (Denmark)

    Williams, P.J.L.; Robinson, C.; Søndergaard, M.;

    1996-01-01

    of 2-3), C-14 uptake into the particulate plus the dissolved fractions approximated to net photosynthesis. Rate constants derived from the chemically determined changes were used to parameterize models that accounted for the respiration of photosynthetic products and for the recycling of respiratory CO......Three sets of comparisons of net and gross inorganic carbon assimilation and C-14 uptake were made with an axenic culture of Skeletonema costatum. The comparisons showed that in the physiological window studied (10-20% of the intrinsic generation time and gross photosynthesis/respiration ratios......2. The conclusion drawn was that over the time scale studied, the C-14 technique was measuring net photosynthesis, consistent with essentially 100% recycling of respiratory CO2. The study has shown that we now possess the basis to make a rigorous analysis of net, gross CO2 fixation and net C-14...

  19. Some chemical synthesis of 14C labelled compounds of pharmaceutical or biological interest

    International Nuclear Information System (INIS)

    The recent discovery of the tuberculostatic properties of the hydrazide of isonicotinic acid (so-called 'Isoniazide', 'Rimifon') has raised considerably its interest, as for metabolic studies which it is more interesting to have it labelled with 14C. We describe in this report the chemical synthesis of 14C carboxyl labelled isoniazide which were done in the pyridine ring to highlight his metabolic function on the Koch's bacillus. (M.B.)

  20. Some chemical synthesis of {sup 14}C labelled compounds of pharmaceutical or biological interest

    Energy Technology Data Exchange (ETDEWEB)

    Pichat, I.; Baret, C.; Audinot, M.; Herbert, M.; Lambin, J. [Commissariat a l' Energie Atomique, Lab. du Fort de Chatillon, Fontenay-aux-Roses (France). Centre d' Etudes Nucleaires

    1955-07-01

    The recent discovery of the tuberculostatic properties of the hydrazide of isonicotinic acid (so-called 'Isoniazide', 'Rimifon') has raised considerably its interest, as for metabolic studies which it is more interesting to have it labelled with {sup 14}C. We describe in this report the chemical synthesis of {sup 14}C carboxyl labelled isoniazide which were done in the pyridine ring to highlight his metabolic function on the Koch's bacillus. (M.B.)

  1. Carbon-14 in neutron-irradiated graphite for graphite-moderated reactors. Joint research

    Energy Technology Data Exchange (ETDEWEB)

    Fujii, Kimio [Japan Atomic Energy Research Inst., Tokai, Ibaraki (Japan). Tokai Research Establishment; Matsuo, Hideto [Radioactive Waste Management and Nuclear Facility Decommissioning Technology Center, Tokyo (Japan)

    2002-12-01

    The graphite moderated gas cooled reactor operated by the Japan Atomic Power Company was stopped its commercial operation on March 1998, and the decommissioning process has been started. Graphite material is often used as the moderator and the reflector materials in the core of the gas cooled reactor. During the operation, a long life nuclide of {sup 14}C is generated in the graphite by several transmutation reactions. Separation of {sup 14}C isotope and the development of the separation method have been recognized to be critical issues for the decommissioning of the reactor core. To understand the current methodologies for the carbon isotope separation, literature on the subject was surveyed. Also, those on the physical and chemical behavior of {sup 14}C were surveyed. This is because the larger part of the nuclides in the graphite is produced from {sup 14}N by (n,p) reaction, and the location of them in the material tends to be different from those of the other carbon atoms. This report summarizes the result of survey on the open literature about the behavior of {sup 14}C and the separation methods, including the list of the literature on these subjects. (author)

  2. Measurement of pion double charge exchange on carbon-13, carbon-14, magnesium-26, and iron-56

    Energy Technology Data Exchange (ETDEWEB)

    Seidl, P.A.

    1985-02-01

    Cross sections for the /sup 13,14/C,/sup 26/Mg,/sup 56/Fe(..pi../sup +/,..pi../sup -/)/sup 13,14/O,/sup 26/Si,/sup 56/Ni reactions were measured with the Energetic Pion Channel and Spectrometer at the Clinton P. Anderson Meson Physics Facility for 120 less than or equal to T/sub ..pi../ less than or equal to 292 MeV and 0 less than or equal to theta less than or equal to 50. The double isobaric analog states (DIAS) are of primary interest. In addition, cross sections for transitions to /sup 14/O(0/sup +/, 5.92 MeV), /sup 14/O(2/sup +/, 7.77 MeV), /sup 56/Ni(gs), /sup 13/O(gs), and /sup 13/O(4.21 MeV) are presented. The /sup 13/O(4.21 MeV) state is postulated to have J/sup ..pi../ = 1/2/sup -/. The data are compared to previously measured double-charge-exchange cross sections on other nuclei, and the systematics of double charge exchange on T greater than or equal to 1 target nuclei leading to the DIAS are studied. Near the ..delta../sub 33/ resonance, cross sections for the DIAS transitions are in disagreement with calculations in which the reaction is treated as sequential charge exchange through the free pion-nucleon amplitude, while for T/sub ..pi../ > 200 MeV the anomalous features of the 164 MeV data are not apparent. This is evidence for significant higher order contributions to the double-charge-exchange amplitude near the reasonable energy. Two theoretical approaches that include two nucleon processes are applied to the DIAS data. 64 references.

  3. Reducing Emissions of Volatile Organic Compounds - Final Report - 08/15/1997 - 02/14/2001

    Energy Technology Data Exchange (ETDEWEB)

    Stensel, H. David; Strand, Stuart E.

    2001-03-14

    The overall objective of this research was to determine if the shallow suspended growth reactor (SSGR) could provide sufficient treatment performance of organic and reduced sulfur (TRS) compounds, at 50 C to meet the EPA ''cluster rule'' regulatory limits. The biodegradation of a mixture of organic compounds that could be present in pulp and paper high volume low concentration gas streams was evaluated at 50 C in a bench-scale SSGR. The removal of methanol was followed in particular, and was mathematically modeled to evaluate the effect of process design and operating parameters on methanol removal. Additional tests were performed to obtain mass transfer and biodegradation kinetic parameters for the model. The acclimation of microbial populations capable of degrading TRS compounds from various seed sources was studied in batch reactors at 30 and 50 C. The degradation of TRS compounds in bench-scale SSGR was studied at 20-50 C. Also, the biodegradation kinetic and mass transfer coefficients for alpha-terpinene and gamma-terpinene were studied. Finally, a pilot plant was constructed and operated at Simpson pulp and paper mill in Tacoma, WA.

  4. Uracil Grafted Carbon Electrode: Electrocatalytic Behavior of Tryptophan, Tyrosine, Catecholamine and Related Compounds

    Institute of Scientific and Technical Information of China (English)

    LIN Xiang-Qin; KANG Guang-Feng; ZHU Xiao-Hong

    2008-01-01

    A uracil grafted glassy carbon electrode (Ura/GCE) was fabricated and characterized by X-ray photoelectron spectroscopy (XPS), cyclic voltammertry (CV) and differential pulse voltammetry (DPV) techniques. The electrochemical behavior of tryptophan (Trp), tyrosine (Tyr), catecholamine such as dopamine (DA), epinephrine (EP) and norepinephrine (NE), and related compounds involving uric acid (UA) and ascorbic acid (AA) at the Ura/GCE was investigated. All these bioactive species could be electrocatalytically oxidized to generate very different current sensitivities. This electrode can be used as a versatile electrochemical sensor for DA, EP, NE, UA, Trp and Tyr determination. The DPV peak potential, current sensitivity, linear range and detection limit of these species were obtained and used for analysis of molecular interactions between uracil and those electroactive species. A mechanism for the surface accumulation was discussed.

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

    Science.gov (United States)

    2008-01-01

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

  6. Carbon-14 immobilization via the CO2-Ba(OH)2 hydrate gas-solid reaction

    International Nuclear Information System (INIS)

    Although no restrictions have been placed on the release of carbon-14, it has been identified as a potential health hazard due to the ease in which it may be assimilated into the biosphere. The intent of the Carbon-14 Immobilization Program, funded through the Airborne Waste Program Management Office, is to develop and demonstrate a novel process for restricting off-gas releases of carbon-14 from various nuclear facilities. The process utilizes the CO2-Ba(OH)2 hydrate gas-solid reaction to directly remove and immobilize carbon-14. The reaction product, BaCO3, possesses both the thermal and chemical stability desired for long-term waste disposal. The process is capable of providing decontamination factors in excess of 1000 and reactant utilization of greater than 99% in the treatment of high volumetric, airlike (330 ppM CO2) gas streams. For the treatment of an air-based off-gas stream, the use of packed beds of Ba(OH)2.8H2O flakes to remove CO2 has been demonstrated. However, the operating conditions must be maintained between certain upper and lower limits with respect to the partial pressure of water. If the water vapor pressure in the gas is less than the dissociation vapor pressure of Ba(OH)2.8H2O, the bed will deactivate. If the vapor pressure is considerably greater, pressure drop problems will increase with increasing humidity as the particles curl and degrade. Results have indicated that when operated in the proper regime, the bulk of the increase in pressure drop results from the conversion of Ba(OH)2.8H2O to BaCO3 and not from the hydration of the commercial Ba(OH)2.8H2O (i.e. Ba(OH)2.7.50H2O) to Ba(OH)2.8H2O

  7. Reexposure and advection of C-14-depleted organic carbon from old deposits at the upper continental slope

    OpenAIRE

    Tesi, Tommaso; Goñi, Miguel A.; Langone, Leonardo; Puig, Pere; Canals, Miquel; Nittrouer, Charles A.; Durrieu De Madron, Xavier; Calafat, Antoni; Palanques, Albert; Heussner, Serge; Davies, Maureen H.; Drexler, Tina M.; Fabres, Joan; Miserocchi, Stefano

    2010-01-01

    Outcrops of old strata at the shelf edge resulting from erosive gravity-driven flows have been globally described on continental margins. The reexposure of old strata allows for the reintroduction of aged organic carbon (OC), sequestered in marine sediments for thousands of years, into the modern carbon cycle. This pool of reworked material represents an additional source of C-14-depleted organic carbon supplied to the ocean, in parallel with the weathering of fossil organic carbon delivered ...

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

    Science.gov (United States)

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

    2016-02-01

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

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

    Science.gov (United States)

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

    2016-07-01

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

  10. [Digital subtraction angiography with carbon dioxide in severe arterial ischemia and allergy to iodinated compounds].

    Science.gov (United States)

    Calvo Cascallo, J; Mundi Salvadó, N; Cardona Fontanet, M

    1993-01-01

    When in some selected patients, a direct arterial surgery (DAS) procedure or an endoluminal surgery (ES) are required for a chronic arterial ischemia (III or IV degrees), and an arteriography with contrast is absolutely contraindicated (because of severe renal failure without hemodialysis program or a severe congestive heart failure or a hyperthyroidism or a seriously demonstrated hypersensibility against the contrast agents); an angiography by digital subtraction with carbon dioxide (DIVAS-CO2) is indicated. This technique provides good quality images with minimal risks for the patient and an adequate study for ulterior treatment. We report a case of a 67-years-old woman, with diabetes-II, ischemic cardiopathy, arterial hypertension and a demonstrated hypersensibility against the iodide compounds. The patient was admitted because of a chronic ischemia (IV degree) with ischemic ulcerations on some fingers from the left foot. High doses of analgesic drugs were needed. Because the hypersensibility against the iodide compounds, an angiography with CO2 was carried out. The good quality images provided by this technique showed the factibility of a revascularization. PMID:8393309

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

    Science.gov (United States)

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

    2012-07-30

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

  12. The kinetics and QSAR of abiotic reduction of mononitro aromatic compounds catalyzed by activated carbon.

    Science.gov (United States)

    Gong, Wenwen; Liu, Xinhui; Gao, Ding; Yu, Yanjun; Fu, Wenjun; Cheng, Dengmiao; Cui, Baoshan; Bai, Junhong

    2015-01-01

    The kinetics of abiotic reduction of mono-nitro aromatic compounds (mono-NACs) catalyzed by activated carbon (AC) in an anaerobic system were examined. There were 6 types of substituent groups on nitrobenzene, including methyl, chlorine, amino, carboxyl, hydroxyl and cyanogen groups, at the ortho, meta or para positions. Our results showed that reduction followed pseudo-first order reaction kinetics, and that the rate constant (logkSA) varied widely, ranging between -4.77 and -2.82, depending upon the type and position of the substituent. A quantitative structure-activity relationship (QSAR) model using 15 theoretical molecular descriptors and partial-least-squares (PLS) regression was developed for the reduction rates of mono-NACs catalyzed by AC. The cross-validated regression coefficient (Qcum(2), 0.861) and correlation coefficient (R(2), 0.898) indicated significantly high robustness of the model. The VIP (variable importance in the projection) values of energy of the lowest unoccupied molecular orbital (ELUMO) and the maximum net atomic charge on the aromatic carbon bound to the nitro group (QC(-)) were 1.15 and 1.01, respectively. These values indicated that the molecular orbital energies and the atomic net charges might play important roles in the reduction of mono-NACs catalyzed by AC in anaerobic systems.

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

    Science.gov (United States)

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

    2009-06-30

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

  14. Modelling of dead carbon fraction in speleothems: a step towards reliable speleothem 14C-chronologies

    Science.gov (United States)

    Lechleitner, Franziska A.; Jamieson, Robert A.; McIntyre, Cameron; Baldini, Lisa M.; Baldini, James U. L.; Eglinton, Timothy I.

    2015-04-01

    Over the past two decades, speleothems have become one of the most versatile and promising archives for the study of past continental climate. Very precise absolute dating is often possible using the U-Th method, resulting in paleoclimate records of exceptional resolution and accuracy. However, not all speleothems are amenable to this dating method for a variety of reasons (e.g. low U concentrations, high detrital Th etc). This has lead researchers to exclude many otherwise suitable speleothems and cave sites from further investigation. 14C-dating of speleothems has so far not been applicable, due to the 'dead carbon' problem. As drip water percolates through the karst, dissolving CaCO3, a variable amount of 14C-dead carbon is added to the solution. This results in a temporally variable and site-specific reservoir effect, ultimately undermining the development of speleothem 14C -chronologies. However, a number of recent studies have shown a clear link between karst hydrology and associated proxies (e.g., Mg/Ca and δ13C) and this 'dead carbon fraction' (DCF). We take advantage of this relationship to model DCF and its changes using Mg/Ca, δ13C and 14C data from published speleothem records. Using one record for calibration purposes, we build a transfer function for the DCF in relation to δ13C and Mg/Ca, which we then apply to other 14C records. Initial model results are promising; we are able to reconstruct general long-term average DCF within uncertainties of the calculated DCF from the U-Th chronology. Large shifts in DCF related to hydrology are also often detected. In a second step, we apply the model to a speleothem from southern Poland, which so far could not be dated, due to very low U-concentrations. To construct a 14C chronology, the stalagmite was sampled at 5 mm intervals. CaCO3 powders were graphitized and measured by Accelerator Mass Spectrometry (MICADAS) at ETH Zurich. Additional high-resolution (0.1 mm/sample) 14C measurements were performed on

  15. 14C Activity and Global Carbon Cycle Changes over the Past 50,000 Years

    Science.gov (United States)

    Hughen, K.; Lehman, S.; Southon, J.; Overpeck, J.; Marchal, O.; Herring, C.; Turnbull, J.

    2004-01-01

    A series of 14C measurements in Ocean Drilling Program cores from the tropical Cariaco Basin, which have been correlated to the annual-layer counted chronology for the Greenland Ice Sheet Project 2 (GISP2) ice core, provides a high-resolution calibration of the radiocarbon time scale back to 50,000 years before the present. Independent radiometric dating of events correlated to GISP2 suggests that the calibration is accurate. Reconstructed 14C activities varied substantially during the last glacial period, including sharp peaks synchronous with the Laschamp and Mono Lake geomagnetic field intensity minimal and cosmogenic nuclide peaks in ice cores and marine sediments. Simulations with a geochemical box model suggest that much of the variability can be explained by geomagnetically modulated changes in 14C production rate together with plausible changes in deep-ocean ventilation and the global carbon cycle during glaciation.

  16. Source terms; isolation and radiological consequences of carbon-14 waste in the Swedish SFR repository

    International Nuclear Information System (INIS)

    The source term, isolation capacity, and long-term radiological exposure of 14C from the Swedish underground repository for low and intermediate level waste (SFR) is assessed. The prospective amount of 14C in the repository is assumed to be 5 TBq. Spent ion exchange resins will be the dominant source of 14C. The pore water in the concrete repository is expected to maintain a pH of >10.5 for a period of at least 106 y. The cement matrix of the repository will retain most of the 14CO32- initially present. Bacterial production of CO2 and CH4 from degradation of ion-exchange resins and bitumen may contribute to 14C release to the biosphere. However, CH4 contributes only to a small extent to the overall carbon loss from freshwater ecosystems. The individual doses to local and regional individuals peaked with 5x10-3 and regional individuals peaked with 5x10-3 and 8x10-4 μSv y-1 respectively at about 2.4x104 years. A total leakage of 8.4 GBq of 14C from the repository will cause a total collective dose commitment of 1.1 manSv or 130 manSv TBq-1. (authors)

  17. Proportion of biogenic carbon in flue gas by carbon-14 measurement - part 2; Biohiili 2

    Energy Technology Data Exchange (ETDEWEB)

    Lehtomaeki, J.; Antson, O.; Hongisto, M. (VTT Technical Research Centre of Finland, Espoo (Finland)) (and others)

    2009-07-01

    The subject of this project is closely related to EU's emissions trading system and to the current and future monitoring needs therein. The determination of fossil part of emissions originated from various fuels by stack measurements or by laboratory analyses could possibly find users also in other fields outside the ETS - Emission Trading Scheme (e.g. waste incineration). After the market analysis and preliminary measurements carried out in the previous Biocarbon project this project focused on the development of the sampling method for stack measurements and to the validation of isotope measurements. The results obtained for fossil proportion of the fuel by current methods will be compared to those obtained by isotope measurements. The operation of the sampling system was tested in long period tests in plant conditions. Moreover, the sample preparation methods and isotope measurements were validated by measuring the proportions of biogenic and fossil carbon of known traffic fuel mixtures. The developed method can also be utilised as a fraud prevention measure related to the expanding international biofuels-trade. (orig.)

  18. Synthesis of carbon C-14 labelled 2-phenyl-4-alpha-alkylaminomethyl-quinolinemethanol: a potential anti-leishmaniasis agent

    Energy Technology Data Exchange (ETDEWEB)

    Wang, T.S.T.; Fawwaz, R.A.; Heertum, R.L.van [Columbia Univ., New York, NY (United States). Coll. of Physicians and Surgeons

    1995-07-01

    Using sodium acetate, [1-{sup 14}C] as a starting material, a total of seven steps were required to synthesize the title compound. This involved acylation of ortho-dichlorobenzene to form dichloroacetophenone, [2-{sup 14}C] (I). The 2-phenyl-4-quinoline carboxylic acid, [2-{sup 14}C] (II) was prepared by the Pfitzinger reaction from (1) and dichloroisatin. Compound 11 was converted to the acid chloride (III) by reaction with SOCl{sub 2} in benzene. Grignard condensation reaction of (III) yielded 4-quinolylmethylketone, [2-{sup 14}C] (IV) which was then converted to the bromomethylketone (V). Compound V was reacted with NaBH{sub 4} to form the ethylene oxide (VI). Alkylation of the oxide yielded the title compound (VII). The overall radiochemical yield was 10.1% and the specific activity was 3.0 mCi/mmol, with a radiochemical purity of >99.5%. (author).

  19. Multimolecular tracers of terrestrial carbon transfer across the pan-Arctic : 14C characteristics of sedimentary carbon components and their environmental controls

    NARCIS (Netherlands)

    Feng, Xiaojuan; Gustafsson, Örjan; Holmes, R. Max; Vonk, Jorien E.; Van Dongen, Bart E.; Semiletov, Igor P.; Dudarev, Oleg V.; Yunker, Mark B.; Macdonald, Robie W.; Wacker, Lukas; Montluçon, Daniel B.; Eglinton, Timothy I.

    2015-01-01

    Distinguishing the sources, ages, and fate of various terrestrial organic carbon (OC) pools mobilized from heterogeneous Arctic landscapes is key to assessing climatic impacts on the fluvial release of carbon from permafrost. Through molecular 14C measurements, including novel analyses of suberin- a

  20. Radiobiological half-lives for carbon-14 and hydrogen-3 leucine in man

    International Nuclear Information System (INIS)

    In vivo estimates of protein metabolism in many are often made by oral or intravenous administration of leucine or its ∼-ketoacid, ∼-ketoisocaproate, labeled with 14C or 3H. Previous estimates of radiation dose from such tracers have been based on the measurement of 14CO2 in breath. Using measurements of the decay of 3H or 14C leucine from plasma proteins, longer biological half-lives for these compounds were obtained. The estimated total-body radiation absorbed dose is 0.97 mrad/uCi for [1-14C]KIC (or [1-14C]leucine) and 0.11 mrad/+Ci for ]4,5-3H]leucine (or [3H]KIC). Assuming administered doses of 100 μCi each, the total-body radiation absorbed dose is still well within the limits set by the FDA for Radioactive Drug Research Committees. 12 references, 3 figures, 3 tables

  1. Validation test for carbon-14 migration and accumulation in a Canadian shield lake

    International Nuclear Information System (INIS)

    This particular BIOMOVS II Technical Report is concerned with modelling the transfer of C-14 through the aquatic food chain following release to a Canadian shield lake. Model performance has been tested against field data supplied by Atomic Energy of Canada Limited. Carbon-14 was added in 1978 to the epilimnion of a small Canadian Shield lake to investigate primary production and carbon dynamics. Data from this experiment were used within BIOMOVS II to provide a validation test, which involved modelling the fate of the C-14 added to the lake. The nature of the spike and the subsequent monitoring allowed the investigation of both short-term processes relevant to evaluation of the impacts of accidental releases as well as longer-term processes relevant to routine release and to solid waste disposal. Four models participated in the scenario: 1) a simple mass balance model of a lake (AECL, Whiteshell Laboratories, Canada); 2) a relatively complex deterministic dynamic compartment model (QuantiSci Ltd.,UK); 3) a complex deterministic model (Studsvik Model A) and a more complex probabilistic model (Studsvik Model B; Studsvik Eco and Safety AB, Sweden). Endpoints were C-14 concentrations in water, sediment and whitefish over a thirteen year period. Each model produced reasonable predictions when compared to the observed data and when uncertainty is taken into consideration. About 0.2 to 0.4% of the initial C-14 inventory to the lakes remained in the water at the end of the study, because of internal recycling of C-14 from sediments. The simple AECL model did not account for this internal recycling of C-14 and, in this respect, its predictions were not as realistic as those of the QuantiSci and Studsvik models for concentrations in water. However, the AECL model predictions for the C-14 inventory remaining in lake sediment were closest to the observed values. Overall, Studsvik Model B was the most accurate in simulating C-14 concentrations in water and in whitefish, but

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

    International Nuclear Information System (INIS)

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

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

    Science.gov (United States)

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

    2016-01-15

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

  4. Redox-active tetrathiafulvalene and dithiolene compounds derived from allylic 1,4-diol rearrangement products of disubstituted 1,3-dithiole derivatives

    OpenAIRE

    Filipe Vilela; Skabara, Peter J; Mason, Christopher R.; Thomas D. J. Westgate; Asun Luquin; Coles, Simon J.; Hursthouse, Michael B.

    2010-01-01

    We present a series of compounds by exploiting the unusual 1,4-aryl shift observed for electron-rich 1,3-dithiole-2-thione and tetrathiafulvalene (TTF) derivatives in the presence of perchloric acid. The mechanistic features of this rearrangement are discussed since this synthetic strategy provides an alternative route for the synthesis and functionalisation of sulfur rich compounds including redox active compounds of TTFs, and a Ni dithiolene.

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

    Science.gov (United States)

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

    2015-06-01

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

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

    Science.gov (United States)

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

    2015-07-01

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

  7. Utilization of Tritium and Carbon-14 in Studies of Isotope Effects

    International Nuclear Information System (INIS)

    The utility of tritium in organic research has been augmented by the development of a simple method for determining C14 and tritium in the same sample. The non-volatile, radioactive material, in a film that is 'infinitely thick' to tritium radiation, is counted in a windowless, gas-fiow proportional counter; the film is then re-counted when covered with a screen that stops all radiation from tritium but allows a fraction of that from C14 to pass. By introduction of one isotope at a point removed from the reaction centre, an isotope effect for the other can be determined from changes in the tritium-C14 ratio in the reactant and/or products as the reaction proceeds. Carriers of reactant, products or derivatives can be added at any point to facilitate isolation, because the analytical method depends primarily on the tritium-C14 ratio. Methods for utilizing the double-label technique will be illustrated by a study of isotope effects in the oxidation of the penultimate carbon of certain labelled polyols with Acetobacter suboxydans. Six D-mannitols position-labelled either with C14 or with tritium at C1, C2 or C3 were prepared. For these, isotope effects (k*/k) of 0.93, 0.23, and 0.71, respectively, were found with C14 at C2, tritium at C2, and tritium at C3; no detectable isotope effects were found for the remaining Dmannitols. In the oxidation of position-labelled D-glucitols, an isotope effect of 0.24 was found for tritium at C5; no detectable effect was found for either C14 or tritium at C1. The techniques are suitable for studying a variety of chemical and biological reactions. (author)

  8. Prise en compte du carbone 14 dans le modèle PASIM

    OpenAIRE

    Duclos, Etienne

    2010-01-01

    J'ai effectué mon stage de fin d'étude d'ingénieur ISIMA au sein de l'Institut National de la Recherche Agronomique (INRA), dans l'Unité de Recherche sur l'Ecosystème Prairial (UREP). Mon stage a été effectué en collaboration avec l'Institut de Radioprotection et de Sûreté Nucléaire (IRSN). J'ai été chargé d'ajouter la gestion du carbone 14 au sein de PaSim, modèle de simulation de prairie gérant déjà les flux de carbone et d'azote. Il m'a donc fallu faire la distinction, au...

  9. Synthesis of {delta}-aminolevulic acid. Application to the introduction of carbon-14 and of tritium; Syntheses de l'acide {delta} aminolevulique. Application a l'introduction de carbone 14 et de tritium

    Energy Technology Data Exchange (ETDEWEB)

    Loheac, J. [Commissariat a l' Energie Atomique, Saclay (France). Centre d' Etudes Nucleaires

    1966-06-01

    Several new syntheses of {delta} aminolevulic acid ({delta} A.L.A.) have been studied. {sup 14}C-4 {delta} - aminolevulic acid has been obtained from {sup 14}C allylacetic carboxylic acid with a yield of 30 per cent with respect to barium carbonate and with a specific activity of 32 mCi/mM. The {sup 14}C-1 or {sup 14}C-2 {delta}-A.L.A. has been prepared from the {sup 14}C-1 or {sup 14}C-2 acetate with a yield of 55 per cent with respect to the acetate. Finally the tritiated {delta}-A.L.A. has been obtained for the first time by tritiation of ethyl phthalimidodehydrolevulate. (author) [French] Plusieurs syntheses nouvelles de l'acide {delta}-aminolevulique ont ete etudiees. L'acide {delta}-aminolevulique {sup 14}C-4 a ete obtenu a partir d'acide allylacetique carboxylique {sup 14}C, avec un rendement global de 30 pour cent par rapport au carbonate de baryum a une activite specifique de 32 mCi/M. Le {delta}-A.A.L. {sup 14}C-1 ou {sup 14}C-2 a ete obtenu a partir d'acetate {sup 14}C-1 ou {sup 14}C-2 avec un rendement de 55 pour cent par rapport a l'acetate. Enfin le {delta}-A.A.L. tritie a ete obtenu pour la premiere fois par tritiation du phtalimidodehydrolevulate d'ethyle. (auteur)

  10. Tritium- and carbon-14-contents of wines of different vintage from the northern and southern hemisphere

    International Nuclear Information System (INIS)

    The carbon-14 and tritium radioactivity contents of up to 19 vintages of German and Southafrican wines were compared. A similar large dependence of the 14C- and of the 3H-activity in the German wine on the nuclear weapon tests of the years 1962/63 was found out. The radioactivity level is also 1977/78 still essentially higher than before 1950. The Southafrican wines have been influenced considerably less by nuclear explosions. The highest 3H-values were found in the vintage 1963 of the German wine with 5910 pCi/litre and in the vintage 1964 of the Southafrican wine with 510 pCi/litre. (orig.)

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

    Directory of Open Access Journals (Sweden)

    Da Sun

    2011-10-01

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

  12. Electrothermal adsorption and desorption of volatile organic compounds on activated carbon fiber cloth.

    Science.gov (United States)

    Son, H K; Sivakumar, S; Rood, M J; Kim, B J

    2016-01-15

    Adsorption is an effective means to selectively remove volatile organic compounds (VOCs) from industrial gas streams and is particularly of use for gas streams that exhibit highly variable daily concentrations of VOCs. Adsorption of such gas streams by activated carbon fiber cloths (ACFCs) and subsequent controlled desorption can provide gas streams of well-defined concentration that can then be more efficiently treated by biofiltration than streams exhibiting large variability in concentration. In this study, we passed VOC-containing gas through an ACFC vessel for adsorption and then desorption in a concentration-controlled manner via electrothermal heating. Set-point concentrations (40-900 ppm(v)) and superficial gas velocity (6.3-9.9 m/s) were controlled by a data acquisition and control system. The results of the average VOC desorption, desorption factor and VOC in-and-out ratio were calculated and compared for various gas set-point concentrations and superficial gas velocities. Our results reveal that desorption is strongly dependent on the set-point concentration and that the VOC desorption rate can be successfully equalized and controlled via an electrothermal adsorption system.

  13. Sorption of organic compounds to activated carbons. Evaluation of isotherm models

    NARCIS (Netherlands)

    Pikaar, I.; Koelmans, A.A.; Noort, van P.C.M.

    2006-01-01

    Sorption to 'hard carbon' (black carbon, coal, kerogen) in soils and sediments is of major importance for risk assessment of organic pollutants. We argue that activated carbon (AC) may be considered a model sorbent for hard carbon. Here, we evaluate six sorption models on a literature dataset for so

  14. Determination of the solubility of Np(IV), Pu(III) - (VI),Am(III) - (VI), and Te(IV), (V) hydroxo compounds in 0.5 - 14 M NaOH solutions

    Energy Technology Data Exchange (ETDEWEB)

    Delegard, C.H.

    1996-09-24

    The solubilities of Am(III), Np(IV), Pu(IV), Tc(IV), Np(V), Pu(V), Am(V), and Tc(V) hydroxo compounds were studied in 0.5 to 14 M NaOH solutions at 25{+-}2 {degrees}C. The effects of fluoride, phosphate, carbonate, oxalate, and some other organic complexing agents on the solubilities of Np(IV), Pu(IV), and TC(IV) hydroxides were investigated at 1.0 and 4.0 M NAOH. Some predictions were made on the dissolved (I.V) and (V) species present in alkali solutions.

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

    Directory of Open Access Journals (Sweden)

    Chung-Yen Lu

    2015-05-01

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

  16. Analysis and Characterization of Organic Carbon in Early Holocene Wetland Paleosols using Ramped Pyrolysis 14C and Biomarkers

    Science.gov (United States)

    Vetter, L.; Schreiner, K. M.; Fernandez, A.; Rosenheim, B. E.; Tornqvist, T. E.

    2014-12-01

    Radiocarbon analyses are a key tool for quantifying the dynamics of carbon cycling and storage in both modern soils and Quaternary paleosols. Frequently, bulk 14C dates of paleosol organic carbon provide ages older than the time of soil burial, and 14C dates of geochemical fractions such as alkali and acid extracts (operationally defined as humic acids) can provide anomalously old ages when compared to coeval plant macrofossil dates. Ramped pyrolysis radiocarbon analysis of sedimentary organic material has been employed as a tool for investigating 14C age spectra in sediments with multiple organic carbon sources. Here we combine ramped pyrolysis 14C analysis and biomarker analysis (lignin-phenols and other cupric oxide products) to provide information on the source and diagenetic state of the paleosol organic carbon. We apply these techniques to immature early Holocene brackish wetland entisols from three sediment cores in southeastern Louisiana, along with overlying basal peats. Surprisingly, we find narrow 14C age spectra across all thermal aliquots from both paleosols and peats. The weighted bulk 14C ages from paleosols and overlying peats are within analytical error, and are comparable to independently analyzed 14C AMS dates from charcoal fragments and other plant macrofossils from each peat bed. Our results suggest high turnover rates of carbon in soils relative to input of exogenous carbon sources. These data raise broader questions about processes within the active soil and during pedogenesis and burial of paleosols that can effectively homogenize radiocarbon content in soils across the thermochemical spectrum. The concurrence of paleosol and peat 14C ages also suggests that, in the absence of peats with identifiable plant macrofossils, ramped pyrolysis 14C analyses of paleosols may be used to provide ages for sea-level indicators.

  17. Mountain scale modeling of transient, coupled gas flow, heat transfer and carbon-14 migration

    International Nuclear Information System (INIS)

    We simulate mountain-scale coupled heat transfer and gas flow at Yucca Mountain. A coupled rock-gas flow and heat transfer model, TGIF2, is used to simulate mountain-scale two-dimensional transient heat transfer and gas flow. The model is first verified against an analytical solution for the problem of an infinite horizontal layer of fluid heated from below. Our numerical results match very well with the analytical solution. Then, we obtain transient temperature and gas flow distributions inside the mountain. These distributions are used by a transient semianalytical particle tracker to obtain carbon-14 travel times for particles starting at different locations within the repository. Assuming that the repository is filled with 30-year-old waste at an initial areal power density of 57 kw/acre, we find that repository temperatures remain above 60 degrees C for more than 10,000 years. Carbon-14 travel times to the surface are mostly less than 1000 years, for particles starting at any time within the first 10,000 years

  18. Effect of carbon dioxide enrichment on health-promoting compounds and organoleptic properties of tomato fruits grown in greenhouse.

    Science.gov (United States)

    Zhang, Zhiming; Liu, Lihong; Zhang, Min; Zhang, Yongsong; Wang, Qiaomei

    2014-06-15

    The objective of the present study was to evaluate the effect of carbon dioxide (CO2) enrichment on the main health-promoting compounds and organoleptic characteristics of tomato (Solanum lycopersicum) fruits grown in greenhouse. The contents of health-promoting compounds, including lycopene, β-carotene, and ascorbic acid, as well as the flavour, indicated by sugars, titrable acidity, and sugar/acid ratio, were markedly increased in CO2 enrichment fruits. Furthermore, CO2 enrichment significantly enhanced other organoleptic characteristics, including colour, firmness, aroma, and sensory attributes in tomato fruits. The results indicated that CO2 enrichment has potential in promoting the nutritional value and organoleptic characteristics of tomatoes.

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

    Energy Technology Data Exchange (ETDEWEB)

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

    2015-06-15

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

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

    Directory of Open Access Journals (Sweden)

    I. Tolosa

    2012-10-01

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

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

  1. Simultaneous determination of nitrophenol isomers at the single-wall carbon nanotube compound conducting polymer film modified electrode

    Institute of Scientific and Technical Information of China (English)

    ZHANG Hui; WANG Zhenhui; ZHOU Shuping

    2005-01-01

    Based on the molecular recognition ability of conductive polymer and the peculiar properties of carbon nanotubes, a novel single wall nanotubes (SWNTs) compound poly(4- aminopyridine) modified electrode (SWNTs/POAPE) is prepared at glass carbon electrode (GCE). The electrochemistry response of nitrophenol isomers is studied at the SWNTs/POAPE. The result indicates that o-, m- and p-nitrophenol are separated entirely at the SWNTs/POAPE interface. The electrode present here can be easily used to determine nitrophenol isomers simultaneously with higher sensitivity.

  2. Synthesis, Characterization, and Biodegradation Studies of Poly(1,4-cyclohexanedimethylene-adipate-carbonates

    Directory of Open Access Journals (Sweden)

    Ajay S. Chandure

    2014-01-01

    Full Text Available Aliphatic/alicyclic poly(1,4-cyclohexanedimethylene-adipate-carbonates (PCACs were synthesized by a transesterification from 1,4-cyclohexamethylendimethanol (1,4-CHDM, adipic acid (AA, diethyl carbonate (DEC, and titanium butoxide Ti(OBu4 as a transesterification catalyst. The synthesized PCACs were characterized by the Fourier transform infrared (FTIR, X-ray diffraction analysis (XRD, solubility, solution viscosity, gel permeation chromatography (GPC, differential scanning calorimetry (DSC, thermogravimetric analysis (TGA, and scanning electron microscope (SEM for their structural, physical, thermal, and morphological investigation. The structure of synthesized PCACs was confirmed by FTIR. All TGA curves of PCACs shows 10% weight loss above 270°C, and they reveal good thermal stability. Biodegradability of PCACs was investigated by hydrolytic degradation at (pH 7.2 and 11.5, enzymatic degradation using Rhizopus delemar lips at 37°C in phosphate buffer solution (PBS, and soil burial degradation at 30°C. The hydrolytic degradation shows the greater rate of weight loss in PBS at pH-11.5 than pH-7.2. The hydrolytic and soil burial degradation shows faster rate of weight loss as compared to enzymatic degradation. Biodegradation rate of PCACs follows the order: PCAC-20 > PCAC-40 > PCAC-60. SEM images show that degradation occurred all over the film surface, creating holes and cracks. These biodegradable PCACs may be able to replace conventional polymer in the fabrication of packaging film in near future.

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

    KAUST Repository

    McMahon, Kelton

    2015-11-21

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

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

    Energy Technology Data Exchange (ETDEWEB)

    Hartwig, J.F.

    1990-12-01

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

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

    International Nuclear Information System (INIS)

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

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

    Institute of Scientific and Technical Information of China (English)

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

    2012-01-01

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

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

    OpenAIRE

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

    2014-01-01

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

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

    OpenAIRE

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

    2015-01-01

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

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

    OpenAIRE

    Choong, Gabriel Y. H.

    2014-01-01

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

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

    Science.gov (United States)

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

    2015-08-01

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

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

    Science.gov (United States)

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

    2015-08-01

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

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

    Science.gov (United States)

    Gustavsson, L; Engwall, M

    2012-01-01

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

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

    Science.gov (United States)

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

    2016-08-21

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

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

    Science.gov (United States)

    Kampf, Christopher; Filippi, Alexander; Hoffmann, Thorsten

    2015-04-01

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

  15. Synthesis of Four Triazole Compounds and Their Corrosion Inhibitive Effect on Carbon Steel in Hydrochloric Acid Medium

    Institute of Scientific and Technical Information of China (English)

    ZHANG Xiao-Ru; XU Min-Hua; ZHANG Shu-Sheng

    2008-01-01

    Four new 1,2,3-triazoles (3a, 3b, 4a and 4b) have been synthesized selectively via click chemistry approach and characterized by elemental analysis, IR, 1H NMR, 13C NMR and single crystal X-ray crystallographic analysis. The inhibiting action of these compounds against the corrosion of carbon steel in 1.0 mol/L HCI solution was investigated by electrochemical techniques including polarization and electrochemical impedance spectroscopy (EIS), both results of which indicate that these compounds act as good anodic inhibitors. The electrochemical study also shows that 4b is the best inhibitor among the four compounds in this work and its efficiency increases with concentration.The obtained highest IE (inhibition efficiency) of 4b is around 97%.

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

    DEFF Research Database (Denmark)

    Trane-Restrup, Rasmus; Jensen, Anker Degn

    2015-01-01

    Steam reforming (SR) and oxidative steam reforming (OSR) of furfural, 2-methylfuran, and guaiacol have been investigated in the temperature range 400-800°C at a steam to carbon (S/C)-ratio of 5 and oxygen to carbon (O/C)-ratio of 0.2-1.4 over Ni/CeO2-K/MgAl2O4. Carbon oxides and H2 were the major...... products in the SR of 2-methylfuran and furfural, while the by-products were methane, ethanol, 2-propanol, and acetone. Temperatures of 500°C or above were needed to minimize the formation of by-products in the SR of 2-methylfuran and furfural. Phenolics, like benzenediols and phenol, were produced in high...... yields in the SR of guaiacol and temperatures of 780°C were needed to totally convert guaiacol to carbon oxides and H2.Carbon deposition was observed in the SR of all three model compounds and was most severe for guaiacol followed by furfural and 2-methylfuran. The carbon deposition could be reduced...

  17. 14CO2-assimilation, translocation of 14C, and 14C-carbonate uptake in different organs of spring barley plants in relation to adult-plant resistance to powdery mildew

    International Nuclear Information System (INIS)

    The cultivar Peruvian of spring barley, which is susceptible at all growth stages, and Asse, which exhibits adult-plant resistance to powdery mildew, were compared in 14CO2 assimilation, distribution of 14C, and 14C-carbonate uptake in different organs of healthy and infected plants. The reduction of 14CO2 assimilation in infected plants at the first and fourth leaf stages was greater in Peruvian than in Asse. In Peruvian, the 14C which was fixed by the infected third leaf of plants with mildew on the lower 3 leaves remained in the third leaves with very little translocation to other parts of the plant. Infection of the lower three leaves at the fourth leaf stage reduced 14CO2 assimilation in noninfected fourth leaves of Asse less than that of Peruvian, but the flow of 14C from the healthy fourth leaves into other plant parts such as leaf sheaths was markedly stimulated in Peruvian compared to Asse. Infection also reduced the uptake of 14C-carbonate by seedling roots, the reduction being greater in Peruvian than Asse. A greater proportion of the 14C absorbed by roots of Asse was translocated to the infected leaves than that of Peruvian. It was concluded that powdery mildew disrupted the normal pattern of photosynthesis and translocation of metabolites in a susceptible cultivar more markedly than in an adult-plant-resistant cultivar of spring barley. (author)

  18. Analysis of Redox Series of Unsymmetrical 1,4-Diamido-9,10-anthraquinone-Bridged Diruthenium Compounds.

    Science.gov (United States)

    Mandal, Abhishek; Hoque, Md Asmaul; Grupp, Anita; Paretzki, Alexa; Kaim, Wolfgang; Lahiri, Goutam Kumar

    2016-03-01

    The unsymmetrical diruthenium complexes [(bpy)2Ru(II)(μ-H2L(2-))Ru(III)(acac)2]ClO4 ([3]ClO4), [(pap)2RuII(μ-H2L(2-))Ru(III)(acac)2]ClO4 ([4]ClO4), and [(bpy)2Ru(II)(μ-H2L(2-))Ru(II)(pap)2](ClO4)2 ([5](ClO4)2) have been obtained by way of the mononuclear precursors [(bpy)2Ru(II)(H3L(-))]ClO4 ([1]ClO4) and [(pap)2Ru(II)(H3L(-))]ClO4 ([2]ClO4) (where bpy = 2,2′-bipyridine, pap = 2-phenylazopyridine, acac(-) = 2,4-pentanedionate, and H4L = 1,4-diamino-9,10-anthraquinone). Structural characterization by single-crystal X-ray diffraction and magnetic resonance (nuclear magnetic resonance (NMR), electron paramagnetic resonance (EPR)) were used to establish the oxidation state situation in each of the isolated materials. Cyclic voltammetry, EPR, and ultraviolet-visible-near-infrared (UV-vis-NIR) spectroelectrochemistry were used to analyze the multielectron transfer series of the potentially class I mixed-valent dinuclear compounds, considering the redox activities of differently coordinated metals, of the noninnocent bridge and of the terminal ligands. Comparison with symmetrical analogues [L2′Ru(μ-H2L)RuL2′](n) (where L′ = bpy, pap, or acac(-)) shows that the redox processes in the unsymmetrical dinuclear compounds are not averaged, with respect to the corresponding symmetrical systems, because of intramolecular charge rearrangements involving the metals, the noninnocent bridge, and the ancillary ligands. PMID:26887785

  19. Introducing the global carbon cycle to middle school students with a 14C research project

    Science.gov (United States)

    Brodman Larson, L.; Phillips, C. L.; LaFranchi, B. W.

    2012-12-01

    Global Climate Change (GCC) is currently not part of the California Science Standards for 7th grade. Required course elements, however, such as the carbon cycle, photosynthesis, and cellular respiration could be linked to global climate change. Here we present a lesson plan developed in collaboration with scientists from Lawrence Livermore National Laboratory, to involve 7th grade students in monitoring of fossil fuel emissions in the Richmond/San Pablo area of California. -The lesson plan is a Greenhouse Gas/Global Climate Change Unit, with an embedded research project in which students will collect plant samples from various locals for analysis of 14C, to determine if there is a correlation between location and how much CO2 is coming from fossil fuel combustion. Main learning objectives are for students to: 1) understand how fossil fuel emissions impact the global carbon cycle, 2) understand how scientists estimate fossil CO2 emissions, and 3) engage in hypothesis development and testing. This project also engages students in active science learning and helps to develop responsibility, two key factors for adolescentsWe expect to see a correlation between proximity to freeways and levels of fossil fuel emissions. This unit will introduce important GCC concepts to students at a younger age, and increase their knowledge about fossil fuel emissions in their local environment, as well as the regional and global impacts of fossil emissions.

  20. In vivo uptake of carbon-14-colchicine for identification of tumor multidrug resistance

    Energy Technology Data Exchange (ETDEWEB)

    Mehta, B.M.; Rosa, E.; Biedler, J.L. [Nuclear Medicine Research Lab., New York, NY (United States)] [and others

    1994-07-01

    A major limitation in the treatment of cancer with natural product chemotherapeutic agents is the development of multidrug resistance (MDR). Multidrug resistance is attributed to enhanced expression of the multidrug resistance gene MDR1. Colchicine (CHC) is known to be one of the MDR drugs. The authors have previously demonstrated that it is possible to distinguish multidrug resistant tumors from the multidrug-sensitive tumors in vivo on the basis of tritium ({sup 3}H) uptake following injection of {sup 3}H-CHC. The present studies were carried out in xenografted animals using {sup 14}C-CHC which may be more indicative of {sup 11}C-labeled CHC distribution with regard to circulating metabolites, since metabolic processes following injection of (ring C, methoxy-{sup 11}C)-CHC may produce significant amounts of circulating 1l-carbon fragments (i.e., methanol and/or formaldehyde). Experiments were carried out at a dose of 2 mg/kg. Activity concentration per injected dose was approximately twice as great in sensitive as in resistant tumors (p < 0.05) at 60 min following intravenous injection of {sup 14}C-CHC. About 75% of total activity was CHC in the sensitive tumors. The findings are further confirmed by the quantitative autoradiographic evaluation of resistant and sensitive tumors. These studies confirm our previous observations that it is possible to noninvasively distinguish multidrug-resistant tumors from sensitive tumors in vivo based on uptake of an injected MDR drug using a{sup 14}C-labeled CHC at the same position and of comparable specific activity to a {sup 11}C-CHC tracer used for PET imaging. 16 refs., 5 figs., 2 tabs.

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

    Science.gov (United States)

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

    2015-12-15

    The main aim of this study was to investigate the single, competitive, and dynamic adsorption of phthalic acid (PA), bisphenol A (BPA), diphenolic acid (DPA), 2,4-dichlorophenoxy-acetic acid (2,4-D), and 4-chloro-2-methylphenoxyacetic acid (MCPA) on two activated carbons with different chemical natures and similar textural characteristics. The adsorption mechanism was also elucidated by analyzing the influence of solution pH and ionic strength. The activated carbons demonstrated high adsorption capacity to remove all micropollutants due to the presence of active sites on their surfaces, which increase dispersive interactions between the activated carbon graphene layers and the aromatic ring of pollutants. The adsorption capacity of the activated carbons increased in the order: DPAadsorption of contaminants is favored at acid pH (pHadsorption sites of the activated carbon.

  2. Oxygen-18 and carbon-13 records for the last 14,000 years from lacustrine carbonates of Siling-Co (lake) in the Qinghai-Tibetan Plateau

    Science.gov (United States)

    Morinaga, H.; Itota, C.; Isezaki, N.; Goto, H.; Yaskawa, K.; Kusakabe, M.; Liu, J.; Gu, Z.; Yuan, B.; Cong, S.

    1993-12-01

    To understand paleoenvironmental changes for the central Qinghai-Tibetan plateau, we analyzed stable isotopes of oxygen and carbon from calcium carbonates in a bottom sediment core collected from Siling-Co (lake). Five conventional and two Tandetron Acceleration Mass Spectrometry (TAMS) C-14 dates indicate that the core recovered sediments of the last 14,000 years. Calcium carbonates in the sediments seem to be primary carbonates precipitated chemically in the lake, and not clastic particles from limestones distributed around the lake, because of large variation of isotopic ratios, isotopic covariance since 6,000 yr BP and similarity between dates from total calcium carbonates and organic carbon. Their isotopic composition therefore reflects that of the lake water. We present the following paleoenvironmental history over the last 14,000 years in the central part of the plateau, from secular variations of delta O-18, delta C-13 and CaCO3 content throughout the core: (1) Desiccation was dominant during the latter part of the Last Glacial stage (14,000 to 11,000 yr BP). (2) The Last Glacial stage abruptly terminated at 11,000 yr BP. (3) A temperate and stable climate was dominant from 11,000 to 5,000 yr BP. (4) Climatic conditions fluctuated from 5,000 to the present, including two strong desiccation periods (5,000 to 4,000 yr BP and 3,000 to 2,000 yr BP) and an intermediate period of heavy rainfall (4,000 to 3,000 yr BP). This period is also characterized by a covariant O and C isotopic trend.

  3. Synthesis of {sup 14}C-labelled hexahydro-1,3,5-trinitro-1,3,5-triazine (RDX), 2,4,6-trinitrotoluene (TNT), nitrocellulose (NC) and glycidyl azide polymer (GAP) for use in assessing the biodegradation potential of these energetic compounds

    Energy Technology Data Exchange (ETDEWEB)

    Ampleman, G.; Thiboutot, S.; Lavigne, J.; Marois, A. [Defence Research Establishment Valcartier, Courcelette, PQ (Canada); Hawari, J.; Jones, A.M.; Rho, D. [National Research Council of Canada, Ottawa, ON (Canada)

    1995-06-01

    Within the framework of an R and D project on bioremediation of soils contaminated with energetic compounds, the biodegradation of energetic products such as hexogen (RDX), trinitrotoluene (TNT), nitrocellulose (NC) and glycidyl azide polymer (GAP) is under study. Microcosm assays must be performed with radioactive carbon-14 labelled products in order to follow the biodegradation process. {sup 14}C-RDX was prepared by nitration of hexamethylenetetramine (HMTA) according to the Hale process. {sup 14}C-ring and methyl labelled TNTs synthesized according to the Dorey and Carper procedure. {sup 14}C-cellulose was synthesized from {sup 14}C-glucose by Acetobacter xylinum. Nitration of the {sup 14}C-cellulose yielded {sup 14}C-nitrocellulose. {sup 14}C-glycidyl azide polymer was obtained by polymerization and azidation of {sup 14}C-epichlorohydrin (ECH) which was synthesized from {sup 14}C-glycerol. Hydrochlorination of {sup 14}C-glycerol and epoxidation of the resulting {sup 14}C-1,3-dichloro 2-propanol yielded {sup 14}C-ECH. The syntheses of these {sup 14}C-labelled explosives are described in this paper. (Author).

  4. A General Method for the Rapid Determination of Carbon-14- and Hydrogen-3-Labelled Substances by Gas Chromatography

    International Nuclear Information System (INIS)

    A method is described for the determination of 14C- and 3H- labelled substances by gas chromatography using different size flow counters. The method of cracking substances in a current of hydrogen gas is especially suitable for 3H-labelled compounds because it is free from the disadvantages encountered when the substances are first oxidized and the water formed subsequently converted. The general applicability of this method is shown for different classes of compounds. The analysis is independent of the chemical composition of the compound. By using a part oi the apparatus very rapid analyses of vaporizable 14C- and apparently all 3H-labelled substances can be made by direct injection into the reaction chamber. The apparatus can also be used for the oxidation procedure. (author)

  5. Electronic structure of the misfit layer compound (LaS)(1.14)NbS2 : Band-structure calculations and photoelectron spectra

    NARCIS (Netherlands)

    Fang, CM; vanSmaalen, S; Wiegers, GA; Haas, C; deGroot, RA

    1996-01-01

    In order to understand the electronic structure of the misfit layer compound (LaS)(1.14)NbS2 we carried out an ab initio band-structure calculation in a supercell approximation. The band structure is compared with that of the components NbS2 and LaS. The calculations show that the electronic structu

  6. Electronic structure of the misfit layer compound (LaS)1.14NbS2 : band-structure calculations and photoelectron spectra

    NARCIS (Netherlands)

    Fang, C.M.; Smaalen, S. van; Wiegers, G.A.; Haas, C.; Groot, R.A. de

    1996-01-01

    In order to understand the electronic structure of the misfit layer compound (LaS)1.14NbS2 we carried out an ab initio band-structure calculation in a supercell approximation. The band structure is compared with that of the components NbS2 and LaS. The calculations show that the electronic structure

  7. Molecular simulation studies of CO2 adsorption by carbon model compounds for carbon capture and sequestration applications.

    Science.gov (United States)

    Liu, Yangyang; Wilcox, Jennifer

    2013-01-01

    Effects of oxygen-containing surface functionalities on the adsorption of mixtures including CO(2)/CH(4), CO(2)/N(2), and CO(2)/H(2)O have been investigated in the current work. Together with Bader charge analysis, electronic structure calculations have provided the initial framework comprising both the geometry and corresponding charge information required to carry out statistical-based molecular simulations. The adsorption isotherms and selectivity of CO(2) from CO(2)/N(2), CO(2)/CH(4), and CO(2)/H(2)O gas mixtures were determined by grand canonical Monte Carlo simulations at temperature/pressure conditions relevant to carbon capture and sequestration applications. The interactions between the surfaces with induced polarity and nonpolar/polar molecules have been investigated. It has been observed that, due to the induced polarity of the surface functionalization, the selectivity of CO(2) over CH(4) increases from approximately 2 to higher than 5, and the selectivity of CO(2) over N(2) increases from approximately 5 to 20, especially in the low-pressure regime. However, water vapor will always preferentially adsorb over CO(2) in carbon-based systems containing oxygen functionalized surfaces at conditions relevant to carbon capture application. Molecular simulation results indicate that the surface chemistry in micropores is tunable thereby influencing the selectivity for enhanced uptake of CO(2).

  8. Diffusion-type model of the global carbon cycle for the estimation of dose to the world population from releases of carbon-14 to the atmosphere

    Energy Technology Data Exchange (ETDEWEB)

    Killough, G.G.

    1977-05-01

    A nonlinear dynamic model of the exchange of carbon among the atmosphere, terrestrial biosphere, and ocean is described and applied to estimating the radiation dose to the world's population from the release of /sup 14/C to the atmosphere from the nuclear power industry. A computer implementation of the model, written in the IBM Continuous System Modeling Program III (CSMP III) simulation language, is presented. The model treats the ocean as a diffusive medium with respect to vertical transport of carbon, and the nonlinear variation of CO/sub 2/ partial pressure with the total inorganic carbon concentration in surface waters is taken into account in calculating the transfer rate from ocean to atmosphere. Transfers between the atmosphere and terrestrial biosphere are represented by nonlinear equations which consider CO/sub 2/ fertilization and impose a constraint on the ultimate total carbon mass in the biosphere.

  9. Pharmacological mechanisms underlying the antinociceptive and tolerance effects of the 6,14-bridged oripavine compound 030418

    Institute of Scientific and Technical Information of China (English)

    Quan WEN; Gang YU; Yu-lei LI; Ling-di YAN; Ze-hui GONG

    2011-01-01

    Aim:To investigate possible pharmacological mechanisms underlying the antinociceptive effect of and tolerance to N-methyl-7α-[(R)-1-hydroxy-1-methyl-3-(thien-3-yi)-propyl]-6,14-endo-ethanotetrahydronororipavine (030418),a derivative of thienorphine.Methods:The binding affinity and efficacy of 030418 were determined using receptor binding and guanosine 5'-0-(3-[35S]thio)triphosphate ([35S]GTPyS) assays in CHO-μ,CHO-κ,CHO-δ,and CHO-ORL1 cell membranes.The analgesic activity of and tolerance to 030418 were evaluated in thermal nociceptive tests in mice.The effects of 030418 on opioid receptors were further investigated using in vivo pharmacological antagonist blockade and in vitro tissue preparations.Results:The compound 030418 displayed high binding affinity to all subtypes of opioid receptors with Ki values in the nanomolar range.In [35S]GTPyS binding assay,the maximal stimulation of 030418 to μ-,κ-,δ-receptors and the ORL1 receptor was 89%,86%,67% and 91%,respectively.In hot-plate test,the antinociceptive effect of 030418 was more potent and longer than morphine.The nonselective opioid receptor antagonist naloxone could completely block 030418-induced antinociception,while both the μ-opioid receptor antagonist β-FNA and the κ-opioid receptor antagonist nor-BNI attenuated 030418-induced antinociception.In contrast,the ORL1 receptor antagonist J-113397 enhanced the antinociceptive effect of 030418.Additionally,chronic treatment with 030418resulted in a dramatic development of tolerance that could not be effectively prevented by J-113397.In guinea pig ileum preparation,the existing action of 030418 could be removed with difficulty after prolonged washing.Conclusion:The compound 030418 is a novel agonist of opioid receptors with high efficiency,long-lasting effect and liability to tolerance,which may be closely correlated with the methyl group at the N17 position and the high hydrophobicity of the C7-thiophene group in its chemical structure.

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

    International Nuclear Information System (INIS)

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

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

    International Nuclear Information System (INIS)

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

  12. carbon Nitride Compounds Synthesized by Thermal Annealing Amorphous Nanostructured Graphite under the Flow of NH3 Gas

    Institute of Scientific and Technical Information of China (English)

    公志光; 李木森

    2003-01-01

    Graphitic-C3N4 (g-C3N4) and pseudocubic-C3N4 (p-C3N4) have been synthesized by thermally annealing highenergy ball milled amorphous nanostructured graphite powders under NH3 atmosphere. The experimental results by x-ray, transmission-electron microscopy, selected electron area diffraction and parallel electron energy loss spectroscopy indicated that g-C3N4 grew from the milled graphite powders in the presence of NH3 gas at a temperature of 1050 ℃. After treatment at a temperature of 1350 ℃, the pseudocubic-C3N4 phase forms. It was believed that the high-energy ball milling generates nanosized amorphous graphite structures, under subsequent isothermal annealing in a flow of NH3 gas, the carbon nitride compound can easily form through reaction of nanostructured carbon with nitrogen of NH3.

  13. CO{sub 2} removal potential of carbons prepared by co-pyrolysis of sugar and nitrogen containing compounds

    Energy Technology Data Exchange (ETDEWEB)

    Arenillas, A.; Drage, T.C.; Smith, K.; Snape, C.E. [University of Nottingham, Fuel Science Group, School of Chemical, Environmental and Mining Engineering, University Park, Nottingham NG7 2RD (United Kingdom)

    2005-08-15

    The nitrogen enrichment of active carbons is reported to be effective in enhancing the specific adsorbate-adsorbent interactions for CO{sub 2}. In this work, nitrogen-enriched carbons were prepared by co-pyrolysis of sugar and a series of nitrogen compounds with different nitrogen functionalities. The results show that although the amount of nitrogen incorporated to the final adsorbent is important, the N-functionality seems to be more relevant for increasing CO{sub 2} uptake. Thus, the adsorbent obtained from urea co-pyrolysis presents the highest nitrogen content but the lowest CO{sub 2} adsorption capacity. However, the adsorbent obtained from carbazole co-pyrolysis, despite the lower amount of N incorporated, shows high CO{sub 2} uptake, up to 9wt.%, probably because the presence of more basic functionalities as determined by XPS analysis.

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

    International Nuclear Information System (INIS)

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

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

    Institute of Scientific and Technical Information of China (English)

    Si-Hai Zhou

    2008-01-01

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

  16. Carbonation rates of peridotite in the Samail Ophiolite, Sultanate of Oman, constrained through 14C dating and stable isotopes

    Science.gov (United States)

    Mervine, Evelyn M.; Humphris, Susan E.; Sims, Kenneth W. W.; Kelemen, Peter B.; Jenkins, William J.

    2014-02-01

    Detailed 14C dating as well as stable C and O isotope analyses were conducted on carbonates formed during alteration of the peridotite layer of the Samail Ophiolite, Sultanate of Oman. 14C results obtained in this and previous studies indicate that surface travertines range in age from modern to >45,000 yr BP, indicating long-term deposition and preservation. Travertine deposition rates in two localities were ˜0.1 to 0.3 mm/yr between ˜30,000 and 45,000 yr BP. Using an estimate of total travertine area, this would result in a maximum of ˜1000 to 3000 m3/yr of travertine being deposited throughout the ophiolite during this time period. This travertine deposition would have sequestered a maximum of ˜1 to 3 × 106 kg CO2/yr. Ca-rich carbonate veins that are associated with the surface travertine deposits have ages ranging from ˜4000 to 36,000 yr BP (average: 15,000 yr BP). Mg-rich carbonate veins exposed in outcrops have ages ranging from ˜8000 to 45,000 yr BP (average: 35,000 yr BP). Detailed sampling from numerous locations (3 locations in this study and 10 locations in the previous studies) indicates that no carbonate veins from the natural peridotite weathering surface are older than the ˜50,000 yr BP dating limit of 14C. However, 14C dating of Mg-rich carbonate veins from three roadcut exposures (Qafeefah, Fanja, and Al-Wuqbah) indicates that a significant number of roadcut veins are 14C dead (>50,000 yr BP). A location weighted average indicates that ˜40% of veins sampled at the three roadcuts are 14C dead. An average including veins sampled at both roadcuts and outcrops indicates that overall ˜8% of Mg-rich carbonate veins are 14C dead. Mg-rich carbonate veins are estimated to sequester on the order of 107 kg CO2/yr throughout the ophiolite.

  17. Release of (14)C-labelled carbon nanotubes from polycarbonate composites.

    Science.gov (United States)

    Rhiem, Stefan; Barthel, Anne-Kathrin; Meyer-Plath, Asmus; Hennig, Michael P; Wachtendorf, Volker; Sturm, Heinz; Schäffer, Andreas; Maes, Hanna M

    2016-08-01

    Waste disposal of carbon nanotube (CNT) containing products is expected to be the most important pathway for release of CNTs into the environment. In the present work, the use of radiolabelled CNTs ((14)C-CNT) for polycarbonate polymer nanocomposites with 1 wt% (14)C-CNT content allowed for the first time to quantify and differentiate the CNT release according to the type of impact along the materials' ageing history. After an initial exposure of the nanocomposite by solar-like irradiation, further environmental impacts were applied to composite material. They aimed at mimicking disposal site conditions that may induce further ageing effects and CNT release. This study included shaking in water, rapid temperature changes, soaking in humic acid solution as well as waste water effluent, and, finally, gentle mechanical abrasion. All ageing impacts were applied sequentially, both on pristine (control) and on solar-irradiated nanocomposites. All experiments were accompanied by absolute quantification of radioactive release as well as chemical and morphological analyses of the nanocomposite surfaces using infra-red (IR) spectroscopy, X-ray photoelectron spectroscopy (XPS) and scanning electron microscopy (SEM). The morphological analysis showed that spectral irradiation can uncover CNT networks on the outer nanocomposite surface layers by polymer degradation. After having subjected the solar-irradiated nanocomposite to all studied disposal site effect, the total radioactive release was quantified to amount to 64 mg CNT/m(2), whereas only 0.8 mg CNT/m(2) were found for the un-irradiated control sample. Solar degradation of polymers was thus found to significantly increase the propensity of the studied polymer nanocomposites to release CNTs during ageing effects at the product's end-of-life typical for disposal sites. PMID:27194367

  18. Elucidating the role of phenolic compounds in the effectiveness of DOM adsorption on novel tailored activated carbon.

    Science.gov (United States)

    Yan, Liang; Fitzgerald, Martha; Khov, Cindy; Schafermeyer, Amy; Kupferle, Margaret J; Sorial, George A

    2013-11-15

    Two novel tailored activated carbons (BC-41-OG and BC-41-MnN) with favorable physicochemical characteristics were successfully prepared for adsorption of dissolved natural organic matter (DOM) by applying systematically chemical and thermal treatment. This research was conducted to investigate the impact of the presence of phenolics on the adsorption capacity of DOM. Isotherm tests were performed for both humic acid (HA) and phenolics on both novel tailored activated carbons and commercial activated carbon F400. The presence of phenolics display a significant effect on hindering the adsorption of HA, however; the physicochemical characteristics of novel activated carbons (surface metal oxides and mesoporosity) can play an important role in alleviating this effect. In contrast, F400, with a relatively lower mesoporosity and surface basicity as compared to the developed adsorbents, was severely impacted by the oligomerization of phenolic compounds. The adsorption capacity of DOM in presence of phenolics was further studied in a continuous flow microcolumn system. The column results showed that both BC-41-OG and BC-41-MnN have not only higher HA adsorption capacity but also better selective adsorption ability than F400.

  19. Distribution of {delta}{sup 14}C in western North Pacific and tracing carbons of human origin

    Energy Technology Data Exchange (ETDEWEB)

    Aramaki, Takafumi; Mizushima, Toshihiko; Togawa, Orihiko [Japan Atomic Energy Research Inst., Mutsu, Aomori (Japan). Mutsu Establishment; Watanabe, Shuichi; Tsunogai, Shizuo [Hokkaido Univ., Sapporo (Japan); Kuji, Tomoyuki [Japan marine Sience Fundation, Mutsu, Aomori (Japan)

    2001-02-01

    Seawater were collected at six points, 0deg to 48degN around 165degE. Dissolved inorganic carbonates was reduced into graphite. The ratio C-11/C-12 was measured by the accelerator mass analyzer. {sup 14}C concentration was calculated from {delta}{sup 13}C value calculated from the {sup 13}C/{sup 12}C ratio. {sup 14}C resulting from the nuclear weapon test was calculated by comparing estimated {sup 14}C and real {sup 14}C concentration. It was compared with that in 1970s. {sup 14}Cbomb has dissolved into North Pacific Intermediate Water in Arctic latitude, which has moved to Mid-latitude. (A. Yamamoto)

  20. Carbon and Oxygen Isotopic Stratigraphy of Mesoproterozoic Carbonate Sequences (1.6–1.4 Ga from Yanshan in North China

    Directory of Open Access Journals (Sweden)

    Kuang Hongwei

    2011-01-01

    Full Text Available In Yanshan, located in the northern part of North China, Mesoproterozoic carbonate sequences (1.6–1.4 Ga form a 10, 000 m thick succession in an aulacogen basin. Carbon and oxygen isotope (δ13O and δ18O, resp. data were obtained from 110 carbonate samples across three sections of these Mesoproterozoic deposits. From the early to late Mesoproterozoic, low negative values of δ13O appear, followed by low positive variation and then a stable increase. An abrupt decrease in δ13O values, with subsequent rapid increase, is found at the end of the Mesoproterozoic. During the whole Mesoproterozoic, δ18O shows a mainly negative trend and occasional highly negative isotopic shifts (from lower to upper deposits. Whole-rock carbon and oxygen isotopic compositions and profiles must be studied to provide a paleogeochemical record that can be associated with paleocean sedimentary environments, temperature, biological productivity, and sea-level fluctuations. Results of the present study correlate well with other international carbon and oxygen isotope profiles, suggesting that a global marine geochemical system existed during the interval of 1.6–1.4 Ga under a globally united tectonic, sedimentary, and geochemical background.

  1. Multimolecular tracers of terrestrial carbon transfer across the pan-Arctic: 14C characteristics of sedimentary carbon components and their environmental controls

    Science.gov (United States)

    Feng, Xiaojuan; Gustafsson, Örjan; Holmes, R. Max; Vonk, Jorien E.; Dongen, Bart E.; Semiletov, Igor P.; Dudarev, Oleg V.; Yunker, Mark B.; Macdonald, Robie W.; Wacker, Lukas; Montluçon, Daniel B.; Eglinton, Timothy I.

    2015-11-01

    Distinguishing the sources, ages, and fate of various terrestrial organic carbon (OC) pools mobilized from heterogeneous Arctic landscapes is key to assessing climatic impacts on the fluvial release of carbon from permafrost. Through molecular 14C measurements, including novel analyses of suberin- and/or cutin-derived diacids (DAs) and hydroxy fatty acids (FAs), we compared the radiocarbon characteristics of a comprehensive suite of terrestrial markers (including plant wax lipids, cutin, suberin, lignin, and hydroxy phenols) in the sedimentary particles from nine major arctic and subarctic rivers in order to establish a benchmark assessment of the mobilization patterns of terrestrial OC pools across the pan-Arctic. Terrestrial lipids, including suberin-derived longer-chain DAs (C24,26,28), plant wax FAs (C24,26,28), and n-alkanes (C27,29,31), incorporated significant inputs of aged carbon, presumably from deeper soil horizons. Mobilization and translocation of these "old" terrestrial carbon components was dependent on nonlinear processes associated with permafrost distributions. By contrast, shorter-chain (C16,18) DAs and lignin phenols (as well as hydroxy phenols in rivers outside eastern Eurasian Arctic) were much more enriched in 14C, suggesting incorporation of relatively young carbon supplied by runoff processes from recent vegetation debris and surface layers. Furthermore, the radiocarbon content of terrestrial markers is heavily influenced by specific OC sources and degradation status. Overall, multitracer molecular 14C analysis sheds new light on the mobilization of terrestrial OC from arctic watersheds. Our findings of distinct ages for various terrestrial carbon components may aid in elucidating fate of different terrestrial OC pools in the face of increasing arctic permafrost thaw.

  2. The history of ironware in Japan revealed by the AMS-carbon 14 age method

    International Nuclear Information System (INIS)

    This paper focuses on the influence what the AMS-carbon 14 age method attains to the history of the iron in the Japanese Islands. The research team in National Museum of Japanese History makes a clear that the Yayoi period began in 10 Cen. cal BC. However, there was a problem in this. It is iron. If the Yayoi period has started in the 10th Cen. BC, it means that the ironware in Japanese Islands had spread early rather than it spreads in China. The research team reexamined the ironware excavated from Magarita site in the Fukuoka Pref. considered to be the oldest ironware in Japan. Consequently, the excavation situation was indefinite and it turned out that we cannot specify the time to belong. Furthermore, 36 ironwares in the initial and early Yayoi were also already found by that time cannot be specified except for two points. Therefore, it turned out that Japanese ironware appeared in the 3rd century of B.C. What does this mean? Although it had been thought that the beginning of agriculture in Japan and the appearance of ironware were simultaneous, it turned out that agriculture has appeared early about in 700 years. Therefore, it became clear that agriculture of Japan started at the Stone Age. (author)

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

    Science.gov (United States)

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

    2016-04-01

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

  4. Evaluation of two decomposition schemes in Earth System Models against LIDET, C14 observations and global soil carbon maps

    Science.gov (United States)

    Ricciuto, D. M.; Yang, X.; Thornton, P. E.

    2015-12-01

    Soils contain the largest pool of carbon in terrestrial ecosystems. Soil carbon dynamics and associated nutrient dynamics play significant roles in regulating global carbon cycle and atmospheric CO2 concentrations. Our capability to predict future climate change depends to a large extent on a well-constrained representation of soil carbon dynamics in ESMs. Here we evaluate two decomposition schemes - converging trophic cascade (CTC) and Century - in CLM4.5/ACME V0 using data from the long-term intersite decomposition experiment team (LIDET), radiocarbon (14C) observations, and Harmonized World Soil Database (HWSD). For the evaluation against LIDET, We exercise the full CLM4.5/ ACME V0 land model, including seasonal variability in nitrogen limitation and environmental scalars (temperature, moisture, O2), in order to represent LIDET experiment in a realistic way. We show that the proper design of model experiments is crucial to model evaluation using data from field experiments such as LIDET. We also use 14C profile data at 10 sites to evaluate the performance of CTC and CENTURY decomposition scheme. We find that the 14C profiles at these sites are most sensitive to the depth dependent decomposition parameters, consistent with previous studies.

  5. Measurement of Carbon Fixation Rates in Leaf Samples — Use of carbon-14 labeled sodium bicarbonate to estimate photosynthetic rates

    OpenAIRE

    sprotocols

    2014-01-01

    Author: David R. Caprette ### Generation of a Light Curve To address the hypothesis concerning photosynthetic efficiency it is necessary to expose sun and shade leaves to a range of light intensities long enough for them to fix significant amounts of carbon. It is necessary to expose identical surface areas under favorable conditions which are identical for all leaves except for light intensity (the experimental variable). A means of measuring the rate of carbon fixation is also neces...

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

    NARCIS (Netherlands)

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

    2005-01-01

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

  7. Synthesis and Structure of a Novel Supramolecular Compound [Co(2,2'-bipy)(H2 O)4 ][trans-1,4-chdc] and Separation of Isomer of 1,4-Cyclohexanedicarboxylic Acid

    Institute of Scientific and Technical Information of China (English)

    2006-01-01

    A supramolecular compound, [Co(2,2'-bipy)(H2O)4][trans-1,4-chdc] (compound 1) (2,2'-bipy=2,2'-bipyridine, 1,4-chdcH2=1,4-cyclohexanedicarboxylic acid), was synthesized and characterized by single-crystal X-ray diffraction analysis, IR spectrometry, TG analysis, and elemental analyses. Single-crystal X-ray diffraction analysis revealed that [Co(2,2'-bipy)(H2O)4]2+ units and adjacent 1,4-chdc2- formed a single layer by hydrogen bonding and electrostatic interactions along the ac-plane, and two symmetry-related single layers interacted with each other by hydrogen bonding, resulting in a double layer, which further formed a 3-D structure by π-π stacking. The most attractive structural feature of compound 1 is that 1,4-chdc2- possesses only trans-conformation although there are both cis- and trans-conformations in the raw material.

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

    Directory of Open Access Journals (Sweden)

    R. Zhu

    2014-01-01

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

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

    Science.gov (United States)

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

    2015-07-22

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

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

    International Nuclear Information System (INIS)

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

  11. Manipulating Ce Valence in RE2Fe14B Tetragonal Compounds by La-Ce Co-doping: Resultant Crystallographic and Magnetic Anomaly.

    Science.gov (United States)

    Jin, Jiaying; Zhang, Yujing; Bai, Guohua; Qian, Zeyu; Wu, Chen; Ma, Tianyu; Shen, Baogen; Yan, Mi

    2016-01-01

    Abundant and low-cost Ce has attracted considerable interest as a prospective alternative for those critically relied Nd/Pr/Dy/Tb in the 2:14:1-type permanent magnets. The (Nd, Ce)2Fe14B compound with inferior intrinsic magnetic properties to Nd2Fe14B, however, cannot provide an equivalent magnetic performance. Since Ce valence is sensitive to local steric environment, manipulating it towards the favorable trivalent state provides a way to enhance the magnetic properties. Here we report that such a desirable Ce valence can be induced by La-Ce co-doping into [(Pr, Nd)1-x(La, Ce)x]2.14Fe14B (0 ≤ x ≤ 0.5) compounds via strip casting. As verified by X-ray photoelectron spectroscopy results, Ce valence shifts towards the magnetically favorable Ce(3+) state in the composition range of x > 0.3, owing to the co-doping of large radius La(3+) into 2:14:1 phase lattice. As a result, both crystallographic and magnetic anomalies are observed in the same vicinity of x = 0.3, above which lattice parameters a and c, and saturation magnetization Ms increase simultaneously. Over the whole doping range, 2:14:1 tetragonal structure forms and keeps stable even at 1250 K. This finding may shed light on obtaining a favorable Ce valence via La-Ce co-doping, thus maintaining the intrinsic magnetic properties of 2:14:1-type permanent magnets. PMID:27457408

  12. Manipulating Ce Valence in RE2Fe14B Tetragonal Compounds by La-Ce Co-doping: Resultant Crystallographic and Magnetic Anomaly

    Science.gov (United States)

    Jin, Jiaying; Zhang, Yujing; Bai, Guohua; Qian, Zeyu; Wu, Chen; Ma, Tianyu; Shen, Baogen; Yan, Mi

    2016-01-01

    Abundant and low-cost Ce has attracted considerable interest as a prospective alternative for those critically relied Nd/Pr/Dy/Tb in the 2:14:1-type permanent magnets. The (Nd, Ce)2Fe14B compound with inferior intrinsic magnetic properties to Nd2Fe14B, however, cannot provide an equivalent magnetic performance. Since Ce valence is sensitive to local steric environment, manipulating it towards the favorable trivalent state provides a way to enhance the magnetic properties. Here we report that such a desirable Ce valence can be induced by La-Ce co-doping into [(Pr, Nd)1−x(La, Ce)x]2.14Fe14B (0 ≤ x ≤ 0.5) compounds via strip casting. As verified by X-ray photoelectron spectroscopy results, Ce valence shifts towards the magnetically favorable Ce3+ state in the composition range of x > 0.3, owing to the co-doping of large radius La3+ into 2:14:1 phase lattice. As a result, both crystallographic and magnetic anomalies are observed in the same vicinity of x = 0.3, above which lattice parameters a and c, and saturation magnetization Ms increase simultaneously. Over the whole doping range, 2:14:1 tetragonal structure forms and keeps stable even at 1250 K. This finding may shed light on obtaining a favorable Ce valence via La-Ce co-doping, thus maintaining the intrinsic magnetic properties of 2:14:1-type permanent magnets. PMID:27457408

  13. The present status of carbon 14 analysis and projects for beryllium 10 analysis at the Tandetron 1 accelerator, Nagoya University

    Energy Technology Data Exchange (ETDEWEB)

    Nakamura, Toshio; Oda, Hirotaka; Ikeda, Akiko; Niu, Etsuko [Nagoya Univ. (Japan)

    2001-02-01

    The operation experience in 1999 of the Tandetron accelerator age estimation system, Nagoya University, is reported, after the overview and the history of the accelerator is briefly described. Total number of carbon 14 environmental samples analyzed was 8567. The project of introducing new HVEE Tandetron for C-14 analysis, and modifying the present GIC Tandetron for Be-10 analysis is presented. Ion source shall be replaced, and the heavy ion detector shall be installed. Projected geological and archaeological studies using Be-10 are enumerated. (A. Yamamoto)

  14. Biochar, activated carbon, and carbon nanotubes have different effects on fate of (14)C-catechol and microbial community in soil.

    Science.gov (United States)

    Shan, Jun; Ji, Rong; Yu, Yongjie; Xie, Zubin; Yan, Xiaoyuan

    2015-10-30

    This study investigated the effects of biochar, activated carbon (AC)-, and single-walled and multi-walled carbon nanotubes (SWCNTs and MWCNTs) in various concentrations (0, 0.2, 20, and 2,000 mg/kg dry soil) on the fate of (14)C-catechol and microbial community in soil. The results showed that biochar had no effect on the mineralization of (14)C-catechol, whereas AC at all amendment rates and SWCNTs at 2,000 mg/kg significantly reduced mineralization. Particularly, MWCNTs at 0.2 mg/kg significantly stimulated mineralization compared with the control soil. The inhibitory effects of AC and SWCNTs on the mineralization were attributed to the inhibited soil microbial activities and the shifts in microbial communities, as suggested by the reduced microbial biomass C and the separated phylogenetic distance. In contrast, the stimulatory effects of MWCNTs on the mineralization were attributed to the selective stimulation of specific catechol-degraders by MWCNTs at 0.2 mg/kg. Only MWCNTs amendments and AC at 2,000 mg/kg significantly changed the distribution of (14)C residues within the fractions of humic substances. Our findings suggest biochar, AC, SWCNTs and MWCNTs have different effects on the fate of (14)C-catechol and microbial community in soil.

  15. Biochar, activated carbon, and carbon nanotubes have different effects on fate of 14C-catechol and microbial community in soil

    Science.gov (United States)

    Shan, Jun; Ji, Rong; Yu, Yongjie; Xie, Zubin; Yan, Xiaoyuan

    2015-10-01

    This study investigated the effects of biochar, activated carbon (AC)-, and single-walled and multi-walled carbon nanotubes (SWCNTs and MWCNTs) in various concentrations (0, 0.2, 20, and 2,000 mg/kg dry soil) on the fate of 14C-catechol and microbial community in soil. The results showed that biochar had no effect on the mineralization of 14C-catechol, whereas AC at all amendment rates and SWCNTs at 2,000 mg/kg significantly reduced mineralization. Particularly, MWCNTs at 0.2 mg/kg significantly stimulated mineralization compared with the control soil. The inhibitory effects of AC and SWCNTs on the mineralization were attributed to the inhibited soil microbial activities and the shifts in microbial communities, as suggested by the reduced microbial biomass C and the separated phylogenetic distance. In contrast, the stimulatory effects of MWCNTs on the mineralization were attributed to the selective stimulation of specific catechol-degraders by MWCNTs at 0.2 mg/kg. Only MWCNTs amendments and AC at 2,000 mg/kg significantly changed the distribution of 14C residues within the fractions of humic substances. Our findings suggest biochar, AC, SWCNTs and MWCNTs have different effects on the fate of 14C-catechol and microbial community in soil.

  16. Bayesian calibration of a soil organic carbon model using Δ14C measurements of soil organic carbon and heterotrophic respiration as joint constraints

    Science.gov (United States)

    Ahrens, B.; Reichstein, M.; Borken, W.; Muhr, J.; Trumbore, S. E.; Wutzler, T.

    2014-04-01

    Soils of temperate forests store significant amounts of organic matter and are considered to be net sinks of atmospheric CO2. Soil organic carbon (SOC) turnover has been studied using the Δ14C values of bulk SOC or different SOC fractions as observational constraints in SOC models. Further, the Δ14C values of CO2 that evolved during the incubation of soil and roots have been widely used together with Δ14C of total soil respiration to partition soil respiration into heterotrophic respiration (HR) and rhizosphere respiration. However, these data have not been used as joint observational constraints to determine SOC turnover times. Thus, we focus on (1) how different combinations of observational constraints help to narrow estimates of turnover times and other parameters of a simple two-pool model, the Introductory Carbon Balance Model (ICBM); (2) whether relaxing the steady-state assumption in a multiple constraints approach allows the source/sink strength of the soil to be determined while estimating turnover times at the same time. To this end ICBM was adapted to model SOC and SO14C in parallel with litterfall and the Δ14C of litterfall as driving variables. The Δ14C of the atmosphere with its prominent bomb peak was used as a proxy for the Δ14C of litterfall. Data from three spruce-dominated temperate forests in Germany and the USA (Coulissenhieb II, Solling D0 and Howland Tower site) were used to estimate the parameters of ICBM via Bayesian calibration. Key findings are as follows: (1) the joint use of all four observational constraints (SOC stock and its Δ14C, HR flux and its Δ14C) helped to considerably narrow turnover times of the young pool (primarily by Δ14C of HR) and the old pool (primarily by Δ14C of SOC). Furthermore, the joint use of all observational constraints made it possible to constrain the humification factor in ICBM, which describes the fraction of the annual outflux from the young pool that enters the old pool. The Bayesian parameter

  17. The crystal structure and physicochemical characteristics of 2-hydroxy-N-[3(5)-pyrazolyl]-1,4-naphthoquinone-4-imine, a new antitrypanosomal compound

    OpenAIRE

    Sperandeo, Norma R.; Karlsson, Alicia; Cuffini, Silvia; Pagola, Silvina; Stephens, Peter W.

    2005-01-01

    This study was designed to investigate the physical characteristics and crystalline structure of 2-hydroxy-N-[3(5)-pyrazolyl]-1,4-naphthoquinone-4-imine (PNQ), a new active compound againstTrypanosoma cruzi, the causative agent of American trypanosomiasis. Methods used included differential scanning calorimetry, thermogravimetry, hot stage microscopy, polarized light microscopy (PLM), Fourier-transform infrared (FTIR) spectroscopy, and high-resolution X-ray powder diffraction (HR-XRPD). Accor...

  18. Validation of ten-minute single sample carbon-14 urea breath test for diagnosis of Helicobacter pylori infection

    Energy Technology Data Exchange (ETDEWEB)

    Prabakaran, K.; Fernandes, V.; McDonald, J. [Illawarra Regional Hospital, Wollongong, NSW (Australia). Depts of Nuclear Medicine and Gastroenterology

    1996-09-01

    Helicobacter pylori infection is traditionally diagnosed by endoscopy followed by gastric biopsy and histologic demonstration of organisms, rapid urease test and culture. The non-invasive carbon-14-urea breath test has been widely accepted now for the diagnosis of this bacterium. This study was aimed to establish and validate normal and abnormal values for an Australian population, for a single sample carbon-14-urea breath test at ten minutes. A dose of 185 kBq was used in order to achieve reasonable counting statistics. The derived values were validated with the results of the rapid urease test. This method has a high sensitivity, specificity and greater patient acceptance, and could be used in many clinical settings as the first modality for the diagnosis of H. pylori infection and for documenting response or cure after antibiotic therapy for eradication. 11 refs., 1 tab., 4 figs.

  19. Validation of ten-minute single sample carbon-14 urea breath test for diagnosis of Helicobacter pylori infection

    International Nuclear Information System (INIS)

    Helicobacter pylori infection is traditionally diagnosed by endoscopy followed by gastric biopsy and histologic demonstration of organisms, rapid urease test and culture. The non-invasive carbon-14-urea breath test has been widely accepted now for the diagnosis of this bacterium. This study was aimed to establish and validate normal and abnormal values for an Australian population, for a single sample carbon-14-urea breath test at ten minutes. A dose of 185 kBq was used in order to achieve reasonable counting statistics. The derived values were validated with the results of the rapid urease test. This method has a high sensitivity, specificity and greater patient acceptance, and could be used in many clinical settings as the first modality for the diagnosis of H. pylori infection and for documenting response or cure after antibiotic therapy for eradication. 11 refs., 1 tab., 4 figs

  20. The use of C-14 as tracer in the carbon flow assimilated by the plants (maize, sugar cane, bean)

    International Nuclear Information System (INIS)

    The flow of carbon in three different crops (maize, beans and sugar cane) was studied by use of C-14. The plants were exposed to an atmosphere with a constant concentration of the tracer for 12 hours in a biosynthesis chamber. The detection of the isotope permitted the distribution and concentration of the photosynthetates in the various organs of the plants to be followed. (M.A.C.)

  1. Year-round probing of soot carbon and secondary organic carbon contributions and sources to the South Asian Atmospheric Brown Cloud using radiocarbon (14C) measurements

    Science.gov (United States)

    Kirillova, Elena; Sheesley, Rebecca J.; Andersson, August; Krusâ, Martin; Safai, P. D.; Budhavant, Krishnakant; Rao, P. S. P.; Praveen, P. S.; Gustafsson, Örjan

    2010-05-01

    South Asia is one region of vital importance for assessing human impact on radiative forcing by atmospheric aerosols. Previous research in the region has indicated that black carbon is a significant component of the regional aerosol load. In contrast, there is more ambiguous information regarding the contribution of secondary organic aerosols (SOA) to the total carbonaceous (TC) aerosol composition. Here we primarily address the SOA component of the South Asian Atmospheric Brown Cloud (ABC) by a combination of measurements of SOA concentrations and the 14C signature of TC. Atmospheric particulate matter was collected during fourteen-month continuous sampling campaigns Jan 2008 - March 2009 at both the Maldives Climate Observatory at Hannimaadho (MCO-H) and at the Sinhagad hilltop sampling site of the Indian Institute of Tropical Meteorology (SIN) in central-western India. The radiocarbon method is an ideal approach to identify fossil sources (14C "dead") compared to biogenic and biomass combustion products (with a contemporary 14C signal). The radiocarbon source apportionment of TC revealed very similar contribution from biogenic/biomass combustion (60-70%) for Indian SIN site and the MCOH receptor regions for much of the year. However, during the summer monsoon season biomass contribution to TC at the Indian Ocean site increases to 70-80%, while it decreases to 40-50% at the Indian site. Source apportionment of a soot carbon (SC) isolate (CTO-375 method; a tracer of black carbon) shows a similar trend. According to preliminary data in summer biomass contribution is higher at the MCOH receptor site (70%) compared to the SIN background site (45%). These unique year-round 14C data will be interpreted in view of the SOA concentration and the varying origin of the air masses.

  2. Photocatalytic Oxidation of Volatile Organic Compounds Over Electrospun Activated TIO2/CARBON Nanofiber Composite

    Science.gov (United States)

    Gholamvand, Zahra; Aboutalebi, Seyed Hamed; Keyanpour-Rad, Mansoor

    In this study, TiO2/PAN-based fibers were prepared by electrospinning a composite solution containing both the desirable contents of TiO2 and a 10 wt. % PAN polymer solution dissolved in N, N-dimethylformamide. The TiO2 loaded electrospun PAN nanofibers were then carbonized at 1000 °C in N2 atmosphere furnace after stabilization at 230 °C in air. Then CNF/TiO2 nanofibers were oxidized at 450 °C in air. The morphology and structure of the TiO2-embeded carbon nanofibers were investigated by SEM and Raman spectroscopy. Specific surface area was determined using BET equation from N2 adsorption analysis. Photocatalytic tests were conducted in a UV illuminated set-up specialized for the filters using ethanol vapor. The results have shown that ethanol vapor was efficiently degraded on TiO2/CNF composite nanofiber mat under UV illumination. The aim of this study was to further investigate the feasibility of TiO2/ACF for practical indoor air purification.

  3. Radiocarbon dating of organic compounds in sediments using preparative capillary gas chromatography (PCGC)

    Energy Technology Data Exchange (ETDEWEB)

    Uchida, Masao [Japan Marine Science and Technology Center, Yokosuka, Kanagawa (Japan); Shibata, Yasuyuki; Yoneda, Minoru; Mukai, Hitoshi; Tanaka, Atsushi; Uehiro, Takashi; Morita, Masatoshi [National Inst. for Environmental Studies, Tsukuba, Ibaraki (Japan); Kawamura, Kimitaka [Hokkaido Univ., Sapporo (Japan); Hirota, Masashi [National Inst. for Environmental Studies, Tsukuba, Ibaraki (Japan)

    2001-02-01

    CG-AMS system, combining two-dimensional gas chromatography and accelerator mass spectroscopy, has been developed for compound-specific carbon 14 measurement. Samples from shallow sea sediments in Sanbanse, Tokyo bay ware collected, six typical fatty acids were separated therefrom. Ages were estimated from the carbon 14 measurement. Acids of carbon number 15 and 16 has nearly contemporary age, whereas acids of carbon number 22 has age of 17000 years. (A. Yamamoto)

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

    Indian Academy of Sciences (India)

    Moamen S Refat; Mohsen M Al-Qahtani

    2011-07-01

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

  5. Simulation of Carbon-14 Migration Through a Thick Unsaturated Alluvial Basin Resulting from an Underground Nuclear Explosion

    Science.gov (United States)

    Martian, P.; Larentzos, J.

    2008-12-01

    Yucca Flat is one of several areas on the Nevada Test Site that was used for underground nuclear testing. Extensive testing performed in the unsaturated and saturated zones have resulted in groundwater contamination and surface subsidence craters in the vicinity of the underground test areas. Simulation of multiphase 14C transport through the thick Yucca Flat alluvial basin was performed to estimate the magnitude of radionuclide attenuation occurring within the unsaturated zone. Parameterization of the 14C transport in the multiphase flow and transport simulator (FEHM) was verified with experimental data collected from a large unsaturated soil column experiment. The experimental data included 14C as a radio-labeled bicarbonate solution, SF6 gas, and lithium bromide solution breakthroughs. Two representative simulation cases with working points located at shallow and deep depths relative to the water table were created to investigate the impact of subsidence crater-enhanced recharge, crater-playa areal extent, gas-phase partitioning, solid-phase partitioning, and a reduced permeability/porosity compressed zone created during the explosion on 14C transport. The representative shallow test had a detonation point located 175 m below land surface, and the deep test had a working point 435 m below land surface in a 500 m deep unsaturated zone. Carbon-14 transport is influenced by gas-phase diffusion and sorption within the alluvium. Gas-phase diffusion is an attenuation mechanism that transports 14C gas as 14CO2 throughout the unsaturated zone and exposes it to a large amount of soil moisture, resulting in dilute concentrations. The simulations indicated that the majority of the 14C inventory remains in the unsaturated zone over a 1,000-year time period after detonation because gas-phase diffusion moves the bulk of the 14C away from the higher recharge occurring in crater playas. Retardation also plays a role in slowing advective aqueous phase transport to the water

  6. Intracellular concentrations and metabolism of carbon compounds in tobacco callus cultures: Effects of light and auxin

    Energy Technology Data Exchange (ETDEWEB)

    Lawyer, A.L.; Grady, K.L.; Bassham, J.A.

    1981-10-01

    Callus cultures derived from pith tissue of Nicotiana tobacum were grown on two media either under continuous illumination or in complete darkness. The first medium limited greening ability of callus grown in the light (3 milligrams per liter naphthalene acetic acid, 0.3 milligram per liter 2-isopentenylaminopurine, Murashige and Skoog salts, and 2% sucrose). The second medium encouraged chlorophyll synthesis (greening) though not shoot formation (0.3 milligram per liter naphthalene acetic acid; 0.3 milligrams per liter 2-isopentylaminopurine). To measure intracellular concentrations, calli were grown for 15 days on these standard media containing (U-/sup 14/C)sucrose. The dry weight proportions of the calli (as a fraction of fresh weight) and many metabolite concentrations nearly doubled in light-grown cells compared to dark-grown cells and increase 30 to 40% on low-auxin media relative to high-auxin media. Glutamine concentrations (from 4 to 26 millimolar) were very high, probably due to the NH/sub 3/ content of the media. Proline concentrations were 20-fold higher in calli grown on low-auxin media in the light (green cells), possibly a stress response to high osmotic potentials in these cells. To analyze sucrose metabolism, callus cells were allowed to take up 0.2% (weight per volume) (U-/sup 14/C)sucrose for up to 90 minutes. In callus tissues and in pith sections from stems of tobacco plants, sucrose was primarily metabolized through invertase activity, producing equal amounts of labeling glucose and fructose. Respiration of /sup 14/CO/sub 2/ followed the labeling patterns of tricarboxylic acid cycle intermediates. Photorespiration activity was low.

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

    International Nuclear Information System (INIS)

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

  8. Use of carbon-14 for the study of elementary carbon exchange between methane and its chemisorption residues on metallic films

    International Nuclear Information System (INIS)

    After giving the results of the most recent work done with a view to providing a rational account of the exchanges between two gases in contact with a catalyst, the authors, using C14, proceed to study elementary exchange between methane and its chemisorption residues on molybdenum films. The surface is labelled in two ways: by chemisorption of C14H4 at different temperatures; or by exchange between C14H4 with a high specific activity and a metallic film previously treated with inactive methane. The C14 is counted in the form of CO2 in the Geiger region. The results show that the exchange rate is measurable from about 100o C onwards and that it reaches a maximum at about 250o C. Furthermore, the exchange is governed by laws which vary according to the prior treatment of the surface. On the basis of the results discussed, the authors suggest a methane displacement pattern which they compare with the CH4 and D2 exchange mechanisms suggested by Kemball. (author)

  9. Characterization of carbon-14 generated by the nuclear power industry. Final report

    International Nuclear Information System (INIS)

    This report describes an evaluation of C-14 production rates in light-water reactors (LWRs) and characterization of its chemical speciation and environmental behavior. The study estimated the total production rate of the nuclide in operating PWRs and BWRs along with the assessment of the C-14 content of solid radwaste. The major source of production of C-14 in both PWR's and BWRs was the activation of 0-17 in the water molecule and of N-14 dissolved in reactor coolant. The production of C-14 was estimated to range from 7 Ci/GW(e)-year to 11 Ci/GW(e)-year. The estimated range of the quantity of C-14 in LLW was 1-2 Ci/ reactor-year which compares favorably with data obtained from shipping manifests. The environmental behavior of C-14 associated with low-level waste (LLW) disposal is greatly dependent upon its chemical speciation. This scoping study was performed to help identify the occurrence of inorganic and organic forms of C-14 in reactor coolant water and in primary coolant demineralization resins. These represent the major source for C-14 in LLW from nuclear power stations. Also, the behavior of inorganic and two of the organic forms of C-14 on soil uptake was determined by measuring distribution coefficients (Kd's) on two soil types and a cement, using two different groundwater types. This study confirms that C-14 concentrations are significantly higher in the primary coolant from PWR stations compared to BWR stations. The C-14 followed trends of Co-60 generation during primary coolant demineralization at all but one of the stations examined. However, the C-14/Co-60 activity ratios measured by this study in resin samples through which samples of coolant were drawn were about 8 to 42 times higher than those reported for waste samples in the industry data base for PWR stations, and 15 to 730 times lower for the BWR stations

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

    Science.gov (United States)

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

    2016-08-15

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

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

    Science.gov (United States)

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

    2004-01-01

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

  12. Highly active and stable hydrogen evolution electrocatalysts based on molybdenum compounds on carbon nanotube-graphene hybrid support.

    Science.gov (United States)

    Youn, Duck Hyun; Han, Suenghoon; Kim, Jae Young; Kim, Jae Yul; Park, Hunmin; Choi, Sun Hee; Lee, Jae Sung

    2014-05-27

    Highly active and stable electrocatalysts for hydrogen evolution have been developed on the basis of molybdenum compounds (Mo2C, Mo2N, and MoS2) on carbon nanotube (CNT)-graphene hybrid support via a modified urea-glass route. By a simple modification of synthetic variables, the final phases are easily controlled from carbide, nitride to sulfide with homogeneous dispersion of nanocrystals on the CNT-graphene support. Among the prepared catalysts, Mo2C/CNT-graphene shows the highest activity for hydrogen evolution reaction with a small onset overpotential of 62 mV and Tafel slope of 58 mV/dec as well as an excellent stability in acid media. Such enhanced catalytic activity may originate from its low hydrogen binding energy and high conductivity. Moreover, the CNT-graphene hybrid support plays crucial roles to enhance the activity of molybdenum compounds by alleviating aggregation of the nanocrystals, providing a large area to contact with electrolyte, and facilitating the electron transfer.

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

    Energy Technology Data Exchange (ETDEWEB)

    Schilling, J.B.

    1997-09-01

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

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

    Directory of Open Access Journals (Sweden)

    V. Dragancea

    2010-12-01

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

  15. Heisenberg behavior of some carbon-beryllium compounds: How well truncated-CI approaches work.

    Science.gov (United States)

    Calzado, Carmen J; Monari, A; Evangelisti, S

    2011-01-30

    This works tries to establish the performance of truncated CI calculations on the evaluation of magnetic coupling parameters with respect to available FCI estimates on a set of carbon-beryllium clusters. First-, second- and third-neighbor magnetic coupling constants have been evaluated and many body effective parameters as the cyclic terms. They result from the fitting of the low-lying states to the eigenvalues of an extended Heisenberg Hamiltonian, involving not only two-body isotropic terms but also cyclic terms. SDCI and DDCI calculations have been carried out and their performance compared with FCI ones. The impact of the basis set choice and size-consistency errors have been explored.

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

    Institute of Scientific and Technical Information of China (English)

    Pierre Le Cloirec

    2012-01-01

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

  17. Double-bed-type extraction needle packed with activated-carbon-based sorbents for very volatile organic compounds.

    Science.gov (United States)

    Ueta, Ikuo; Samsudin, Emi Liana; Mizuguchi, Ayako; Takeuchi, Hayato; Shinki, Takumi; Kawakubo, Susumu; Saito, Yoshihiro

    2014-01-01

    A novel needle-type sample preparation device was developed for the determination of very volatile organic compounds (VVOCs) in gaseous samples by gas chromatography-mass spectrometry (GC-MS). Two types of activated-carbon-based sorbents, Carbopack X and a carbon molecular sieve (CMS), were investigated as the extraction medium. A double-bed-type extraction needle showed successful extraction and desorption performance for all investigated VVOCs, including acetaldehyde, isoprene, pentane, acetone, and ethanol. Sensitive and reliable determination of VVOCs was achieved by systematically optimizing several desorption conditions. In addition, the effects of sample humidity on the extraction and desorption of analytes were investigated with the needle-type extraction devices. Only the CMS packed extraction needle was adversely affected by sample humidity during the desorption process; on the other hand the double-bed-type extraction needle was unaffected by sample humidity. Finally, the developed double-bed-type extraction needle was successfully applied to the analysis of breath VVOCs of healthy subjects. PMID:24176747

  18. Theoretical investigation of a novel high density cage compound 4,8,11,14,15-pentanitro-2,6,9,13-tetraoxa-4,8,11,14,15-pentaazaheptacyclo[5.5.1.1(3,11).1(5,9)] pentadecane.

    Science.gov (United States)

    Lin, He; Zhu, Shun-guan; Zhang, Lin; Peng, Xin-hua; Chen, Peng-yuan; Li, Hong-zhen

    2013-03-01

    A novel polynitro cage compound 4,8,11,14,15-pentanitro-2,6,9,13-tetraoxa-4,8,11,14,15-pentaazaheptacyclo [5.5.1.1(3,11).1(5,9)]pentadecane(PNTOPAHP) has been designed and investigated at the DFT-B3LYP/6-31(d) level. Properties, such as electronic structure, IR spectrum, heat of formation, thermodynamic properties and crystal structure have been predicted. This compound is most likely to crystallize in C2/c space group, and the corresponding cell parameters are Z = 8, a = 29.78 Å, b = 6.42 Å, c = 32.69 Å, α = 90.00°, β = 151.05°, γ = 90.00° and ρ = 1.94 g/cm(3). In addition, the detonation velocity and pressure have also been calculated by the empirical Kamlet-Jacobs equation. As a result, the detonation velocity and pressure of this compound are 9.82 km/s, 44.67 GPa, respectively, a little higher than those of 4,10-dinitro-2,6,8,12-tetraoxa-4,10-diazaisowurtzitane(TEX, 9.28 km/s, 40.72 GPa). This compound has a comparable chemical stability to TEX, based on the N-NO(2) trigger bond length analysis. The bond dissociation energy ranges from 153.09 kJ mol(-1) to 186.04 kJ mol(-1), which indicates that this compound meets the thermal stability requirement as an exploitable HEDM. PMID:23111684

  19. Oxygène-18, carbone-13, carbone-14 et diatomées dans les quatre carottes du lac Huynamarca (Bolivie) : premiers résultats

    OpenAIRE

    Wirrmann, Denis; Servant Vildary, Simone; Fontes, J.C.

    1982-01-01

    L'étude de géochimie isotopique des carbonates coquilliers de quatre carottes du lac Huynamarca (Bolivie), ainsi que les datations au carbone-14 de quelques échantillons montrent qu'au cours des dix derniers millénaires le bilan hydrologique du lac Titicaca a considérablement varié. Une phase sèche, située entre 3650 et 5325 ans B.P. se traduit par une baisse du niveau du lac d'au moins dix mètres par rapport à l'actuel, avec comme corrolaire l'augmentation de la teneur en sels dissous dans l...

  20. Estimation of groundwater residence time using environmental radioisotopes (14C,T) in carbonate aquifers, southern Poland.

    Science.gov (United States)

    Samborska, Katarzyna; Różkowski, Andrzej; Małoszewski, Piotr

    2013-01-01

    Triassic carbonate aquifers in the Upper Silesia region, affected by intense withdrawal, have been investigated by means of isotopic analyses of (14)C, δ(13)C, δ(2)H, δ(18)O and (3)H. The isotopic examinations were carried out in the 1970s and in the early 1980s, and it was the first application of tracers to estimate age and vulnerability for the contamination of groundwater in this region. Similar isotopic analyses were conducted in 2007 and 2008 with the same Triassic carbonate formation. The isotopic examinations were performed within the confined part of the carbonate formation, wherein aquifers are covered by semi-permeable deposits. The direct recharge of the aquifer occurs in the outcrop areas, but it mainly takes place due to percolation of the water through aquitards and erosional windows. The Triassic aquifer has been intensively drained by wells and by lead-zinc mines. Nowadays, the declining water demand and closure of some mines have induced a significant increase in the water table level. The detailed analysis of the results, including the radiocarbon age corrections and the comparison of radioisotope activities, has made it possible to estimate the range of residence time within the carbonate Triassic aquifer. This range from several tens to several tens of thousands indicates that the recharge of aquifers might have occurred between modern times and the Pleistocene. The apparent age of the water estimated on the basis of (14)C activity was corrected considering the carbon isotope exchange and the diffusion between mobile water in fractures and stagnant water in micropores. The obtained corrected period of recharge corresponds to the result of investigations of noble gases, which were carried out in the 1990s. In almost half of the cases, groundwater is a mixture of young and old water. The mixing processes occur mainly in areas of heavy exploitation of the aquifer.

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

    Science.gov (United States)

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

    2015-11-01

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

  2. Measurement of low level carbon-14 in biologic specimens by wet ashing

    Energy Technology Data Exchange (ETDEWEB)

    Bucks, D.; Maibach, H.

    1981-10-01

    Pharmacokinetic studies of animal and human skin are often advantageously performed with low levels of C-14. We detail an efficient wet ashing mehtod capable of detecting 20 dpm per sample, equivalent to twice the background level, thus permitting complete kinetic assays with 1 ..mu..Ci or less of C-14 per subject.

  3. Oxygen electrode reaction in molten carbonate fuel cells. Final report, September 15, 1987--September 14, 1990

    Energy Technology Data Exchange (ETDEWEB)

    Appleby, A.J.; White, R.E.

    1992-07-07

    Molten carbonate fuel cell system is a leading candidate for the utility power generation because of its high efficiency for fuel to AC power conversion, capability for an internal reforming, and a very low environmental impact. However, the performance of the molten carbonate fuel cell is limited by the oxygen reduction reaction and the cell life time is limited by the stability of the cathode material. An elucidation of oxygen reduction reaction in molten alkali carbonate is essential because overpotential losses in the molten carbonate fuel cell are considerably greater at the oxygen cathode than at the fuel anode. Oxygen reduction on a fully-immersed gold electrode in a lithium carbonate melt was investigated by electrochemical impedance spectroscopy and cyclic voltammetry to determine electrode kinetic and mass transfer parameters. The dependences of electrode kinetic and mass transfer parameters on gas composition and temperature were examined to determine the reaction orders and the activation energies. The results showed that oxygen reduction in a pure lithium carbonate melt occurs via the peroxide mechanism. A mass transfer parameter, D{sub O}{sup 1/2}C{sub O}, estimated by the cyclic voltammetry concurred with that calculated by the EIS technique. The temperature dependence of the exchange current density and the product D{sub O}{sup 1/2}C{sub O} were examined and the apparent activation energies were determined to be about 122 and 175 kJ/ mol, respectively.

  4. Differentiation of Pigment in Eggs Using Carbon ((13)C/(12)C) and Nitrogen ((15)N/(14)N) Stable Isotopes.

    Science.gov (United States)

    Sun, Feng M; Shi, Guang Y; Wang, Hui W

    2016-07-01

    Consumers prefer natural and healthy food, but artificial pigments are often abused in egg products. The study aimed at differentiating the origin of pigments in eggs by applying the technique of carbon ((13)C/(12)C) and nitrogen ((15)N/(14)N) stable isotope analysis. Five hundred sixty laying hens were randomly distributed into 14 treatments, which were divided into four groups: maize, carophyll red pigment, carophyll yellow pigment, and a mixture of carophyll red and yellow pigments. Eggs were collected and pretreated to determe the values of the Roche Yolk Color Fan (RCF), δ(13)C, and δ(15)N. With increasing maize content, the RCF and δ(13)C values of yolks increased. Moreover, the RCF values in the three pigment groups were significantly influenced by the artificial colors, but δ(13)C values were not significantly different, regardless of the existence of pigment. The δ(15)N values in all treatments did not vary as regularly as the carbon stable isotope. A strong positive correlation was found between RCF and δ(13)C in the maize group, but no such correlation was be observed in the pigment groups. It is concluded that carbon stable isotope ratio analysis (δ(13)C) of the yolk can be used to differentiate the origin of the pigment added to eggs.

  5. Differentiation of Pigment in Eggs Using Carbon ((13)C/(12)C) and Nitrogen ((15)N/(14)N) Stable Isotopes.

    Science.gov (United States)

    Sun, Feng M; Shi, Guang Y; Wang, Hui W

    2016-07-01

    Consumers prefer natural and healthy food, but artificial pigments are often abused in egg products. The study aimed at differentiating the origin of pigments in eggs by applying the technique of carbon ((13)C/(12)C) and nitrogen ((15)N/(14)N) stable isotope analysis. Five hundred sixty laying hens were randomly distributed into 14 treatments, which were divided into four groups: maize, carophyll red pigment, carophyll yellow pigment, and a mixture of carophyll red and yellow pigments. Eggs were collected and pretreated to determe the values of the Roche Yolk Color Fan (RCF), δ(13)C, and δ(15)N. With increasing maize content, the RCF and δ(13)C values of yolks increased. Moreover, the RCF values in the three pigment groups were significantly influenced by the artificial colors, but δ(13)C values were not significantly different, regardless of the existence of pigment. The δ(15)N values in all treatments did not vary as regularly as the carbon stable isotope. A strong positive correlation was found between RCF and δ(13)C in the maize group, but no such correlation was be observed in the pigment groups. It is concluded that carbon stable isotope ratio analysis (δ(13)C) of the yolk can be used to differentiate the origin of the pigment added to eggs. PMID:27302905

  6. Single crystal study on a novel Kondo compound Ce{sub 6}Pt{sub 11}In{sub 14}

    Energy Technology Data Exchange (ETDEWEB)

    Pikul, A.P. E-mail: a.pikul@int.pan.wroc.pl; Bukowski, Z.; Stepien-Damm, J.; Kaczorowski, D

    2004-05-01

    Ce{sub 6}Pt{sub 11}In{sub 14} crystallizes with a monoclinic unit cell (space group C2/m; lattice parameters: a=22.729(5) A, b=4.3960(10) A, c=14.780(3) A, {beta}=118.35(3) deg.; Z=2). It is paramagnetic down to 1.9 K, and strongly anisotropic in the entire temperature range studied. The electrical resistivity along the b-axis shows Kondo features with a maximum located at 7 K. The transverse magnetoresistivity isotherms, measured in the incoherent region, follow a single-ion Kondo scaling with the characteristic temperature T*=4 K.

  7. Role of carbon-carbon phenyl migration in the pyrolysis mechanism of β-O-4 lignin model compounds: phenethyl phenyl ether and α-hydroxy phenethyl phenyl ether.

    Science.gov (United States)

    Beste, Ariana; Buchanan, A C

    2012-12-20

    We investigate phenyl shift and subsequent β-scission reactions for PhCHXCH·OPh [X = H, OH], which are part of the pyrolysis mechanism of phenethyl phenyl ether (PPE) and α-hydroxy PPE. PPE and its derivatives are model compounds for the most common linkage in lignin, the β-O-4 linkage. We use density functional theory to locate transition states and equilibrium structures and kinetic Monte Carlo in combination with transition-state theory for kinetic simulations. Oxygen-carbon and carbon-carbon phenyl shift reactions proceed through cyclic intermediates with similar barriers. However, while subsequent β-scission of the oxygen-carbon shift products proceeds with virtually no barrier, the activation energy for β-scission of the carbon-carbon shift products exceeds 15 kcal/mol. We found that about 15% of β-radical conversion can be attributed to carbon-carbon shift for PPE and α-hydroxy PPE at 618 K. Whereas the oxygen-carbon shift reaction has been established as an integral part of the pyrolysis mechanism of PPE and its derivatives, participation of the carbon-carbon shift reaction has not been shown previously.

  8. Interaction of pinaverium (a quaternary ammonium compound) with 1,4-dihydropyridine binding sites in rat ileum smooth muscle.

    OpenAIRE

    Feron, Olivier; Wibo, Maurice; Christen, M O; Godfraind, Theophile

    1992-01-01

    1. The interaction of pinaverium bromide, a quaternary ammonium compound, with binding sites for (L-type) calcium channel blockers was investigated in rat ileum smooth muscle. 2. Pinaverium inhibited [3H]-(+)-PN200-110 ([3H]-(+)-isradipine) specific binding to tissue homogenates incompletely (Ki 0.38 microM; maximal inhibition 80%). In contrast, binding to single cell preparations (obtained by collagenase treatment) and to saponin-treated homogenates was completely inhibited. These data are c...

  9. Preliminary study of the impact of tritium and carbon 14 releases from the Saint-Alban nuclear power plant. CRIIRAD N.04-20 V1 Report

    International Nuclear Information System (INIS)

    After having recalled the results of previous studies on the radioactivity in surface water and land environments, and outlined the need of an investigation of the tritium and carbon 14 contamination, this report defines the objectives of this investigation, the adopted methodology (choice of plants, tritium and carbon 14 dose measurements, and sampling to study time variations). It recalls some aspects of tritium and carbon 14 releases (production of radionuclides, origins of emissions in the environment, assessments by EDF). It reports the investigation and the assessment of tritium activity in a land environment and in rain waters about the investigated site, and the investigation and the assessment of carbon 14 activity within the same environment. It reports preliminary results concerning the aquatic environment

  10. Design, synthesis and nonlinear optical properties of (E)-1-(4-substituted)-3-(4-hydroxy-3-nitrophenyl) prop-2-en-1-one compounds

    Science.gov (United States)

    Saha, Amrita; Shukla, Vijay; Choudhury, Sudip; Jayabalan, J.

    2016-06-01

    A new series of (E)-1-(4-substituted)-3-(4-hydroxy-3-nitrophenyl) prop-2-en-1-one compounds have been synthesized by Claisen-Schmidt condensation reaction. Nonlinear optical characterization were carried out using z-scan technique with nanosecond pulses. These samples are found to exhibit strong nonlinear absorption at 532 nm and the nonlinear absorption coefficient of these samples exponentially increases with the increase of phonon characteristic energy. This relation speaks the role of phonon in the origin of nonlinear absorption in these compounds. The reported dependence of optical nonlinearity of the chalcone derivatives on the phonon characteristic energy will help in designing similar class of new molecules with high nonlinear coefficients.

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

    Energy Technology Data Exchange (ETDEWEB)

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

    2009-03-01

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

  12. Effect of substitutions on 3d magnetism in Gd2Fe14-xMxC compounds, with M=Ni, Si, Cu or V

    International Nuclear Information System (INIS)

    Results of magnetic measurements and 57Fe Moessbauer spectroscopy performed on Gd2Fe14-xMxC compounds, with M=Ni, Si, Cu or V are presented. As M is substituted for Fe, the six crystallographically inequivalent iron sites split into seven inequivalent sites for M=Si, Cu, V, or eight for M=Ni. The analysis of the hyperfine fields and relative intensities supports a preferential distribution of the substitutional elements on the Fe lattice sites. The effects of the substitutional elements on Curie temperatures and anisotropy fields as well as on Fe hyperfine parameters are discussed on the grounds of the preferential Fe site occupancy. (orig.)

  13. Spatial Distribution and Dynamics of Carbon-14 in a Wetland Ecosystem

    Energy Technology Data Exchange (ETDEWEB)

    Yankovich, Tamara L. [International Atomic Energy Agency, P.O. Box 100, 1400 Vienna (Austria); Carr, James; King-Sharp, K.; Doug Killey, R.W. [Atomic Energy of Canada Limited, Chalk River Laboratories, Chalk River, Ontario, K0J 1J0 (Canada); Robertson, Erin [201 21st Street East, Saskatoon, SK S7K 0B8 (Canada); Beresford, Nicholas A. [NERC Centre for Ecology and Hydrology, Lancaster Environment Center, Bailrigg, Lancaster, LA14AP (United Kingdom); School of Environment and Life Sciences, University of Salford, Manchester, M44WT (United Kingdom); Wood, Michael D. [School of Environment and Life Sciences, University of Salford, Manchester, M44WT (United Kingdom)

    2014-07-01

    There is significant interest in assessing the impact of {sup 14}C releases from nuclear facilities, radioactive waste management areas, and geologic disposal facilities. As a result, there is a general need to gain understanding of {sup 14}C dynamics, especially in complex interface ecosystems, such as wetlands. This paper summarizes the key findings of two studies undertaken in Duke Swamp, a circa 0.1 km{sup 2} area of wetland consisting of marsh, fen and swamp habitats, on the Atomic Energy of Canada Limited (AECL)'s Chalk River Laboratories Site. The swamp receives radionuclides, such as {sup 14}C and tritium, from an up-gradient waste management area. The first study was an extensive field sampling campaign, involving collection of surface vegetation at 69 locations on a 50 m x 50 m grid, to evaluate the spatial distribution of {sup 14}C in Duke Swamp. Representative receptor plants and animals, and corresponding environmental media (including air, soil, and plant) samples were then collected, as part of a second study, at a subset of six locations with {sup 14}C specific activities that spanned the range present in Duke Swamp and also represented the different wetland habitats occurring there. The highest specific activity concentrations in surface vegetation were highly localized, representing a surface area of only about 150 m{sup 2}. The spatial distribution of {sup 14}C in the swamp seemed to be at least partly accounted for by the physical attributes of the Duke Swamp habitat. In general, it was found that specific activities of {sup 14}C in biota tissues reflected those measured in surface vegetation collected from the same sampling location. Such information provides needed insight for biosphere assessments, as well as for the development of monitoring programs that demonstrate protection of biota in areas where exposure to {sup 14}C is elevated. (authors)

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

    Directory of Open Access Journals (Sweden)

    Jean-François Feller

    2014-01-01

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

  15. [Tritium- and carbon-14-contents of wines of different vintage from the northern and southern hemisphere (author's transl)].

    Science.gov (United States)

    Fischer, E; Möller, H; Rapp, A; Steffan, H

    1980-10-01

    The carbon-14 and tritium radioactivity contents of up to 19 vintages of German and South African wines were compared. A similar large dependence of the 14C- and of the 3H-activity in the German wine on the nuclear weapon tests of the years 1962/63 was found out. The radioactivity level is also 1977/78 still essential higher than before 1950. The South African wines have been influenced considerably smaller by nuclear explosions. The highest 3H-values were found in the vintage 1963 of the German wine with 5910 pCi/litre and in the vintage 1964 of the South African wine with 510 pCi/litre.

  16. Characteristics of compound multiplicity in 28Si-Em interactions at 14.6 A GeV

    International Nuclear Information System (INIS)

    The multiplicity of charged particles in high energy nucleus-nucleus interactions is an important parameter which indicates how many particles are produced in that interaction. The multiplicity distributions of produced particles help in learning the interaction mechanism. Generally, it is accepted that in high energy nucleus-nucleus collisions, the emission of fast target associated particles mostly the knocked out protons known as grey particles, takes place at a relatively latter stage of the collision. These fast protons with range L ≥3 mm and relative velocity 0.3 ≤ β ≤0.7 lies in the energy range 30-400 MeV. Moreover, these grey particles (Ng) are often assumed to be the measure of the number of encounters made by the incident hadron inside the target nucleus. Also the particles produced in the first stage of collision with relative velocity β ≥0.7 are known as relativistic shower particles (Ns). These particles are mostly pions with a small admixture of charged K-mesons and fast protons. The analysis of the experimental data in terms of multiplicity distributions for grey and shower particles collectively known as compound multiplicity (i.e. Nc = Ng + Ns) introduced by Jurak and Linscheid is one of the main source of information about the mechanism of particle production. Many workers analyzed the data on nucleus-nucleus (A-A) and h-A collisions to investigate some interesting features of compound multiplicity distribution

  17. Concentration and 14C Content of Total Organic Carbon and Black Carbon in Small (<100 ug C) Samples from Low-Latitude Alpine Ice Cores

    Science.gov (United States)

    Kehrwald, N. M.; Czimczik, C. I.; Santos, G. M.; Thompson, L. G.; Ziolkowski, L.

    2008-12-01

    Many low latitude glaciers are receding with consequences for the regional energy budget and hydrology. Ice loss has been linked to climate change and the deposition of organic aerosols such as black carbon (BC) which is formed during incomplete combustion. Little is known about how the contents of BC and total organic carbon (TOC) in aerosols change over time and how anthropogenic activities (e.g. land-use change) impact this variability. Low-latitude ice cores are located closer to population centers than polar ice caps and can provide a regional synthesis of TOC and BC variability. Radiocarbon (14C) may be used to partition BC aerosols into fossil (>50 kyrs) and modern sources (e.g. fossil-fuels vs. wildfires). We quantified TOC, BC, and their 14C content in three low-latitude ice cores: Naimona'nyi (30°27'N, 81°91'E) and Dasuopu (28°23'N, 85°43'E), Tibet, and Quelccaya (13°56'S; 70°50'W), Peru. Aerosols (52-256 g ice on filters) were separated into TOC and BC using thermal oxidation (CTO- 375). 14C was measured by AMS. TOC contents were 0.11-0.87, 0.05-0.43, and 0.06-0.19 μg C (g ice) -1 for Naimona'nyi, Dasuopu, and Quelccaya, respectively. BC contents were 18±8, 27±4, and 29±12 %TOC. Procedural blanks were 0.8 ± 0.4 μg C (TOC) and 1.2 ± 0.6 μg C (BC). In ice cores well dated through annual layer counting and/or independent ages (e.g. volcanic horizons) such as Quelccaya, the ability to separate BC from TOC, as well as partition BC into fossil and modern contributions has potential for reconstructing pre- and post-industrial changes in aerosol composition and their impact on the energy budget.

  18. Carbon and 14C distribution in tropical and subtropical agricultural soils

    Science.gov (United States)

    Prastowo, Erwin; Grootes, Pieter; Nadeau, Marie

    2016-04-01

    Paddy soil management affects, through the alternating anoxic and oxic conditions it creates, the transport and stabilisation of soil organic matter (SOM). Irrigation water may percolate more organic materials - dissolved (DOM) and colloidal - into the subsoil during anoxic conditions. Yet a developed ploughpan tends to prevent C from going deeper in the subsoil and partly decouple C distribution in top and sub soil. We investigate the influence of different soil type and environment. We observed the C and 14C distribution in paddy and non-paddy soil profiles in three different soil types from four different climatic regions of tropical Indonesia, and subtropical China. Locations were Sukabumi (Andosol, ca. 850 m a.s.l), Bogor (clayey Alisol, ca. 240 m a.s.l), and Ngawi (Vertisol, ca. 70 m a.s.l) in Jawa, Indonesia, and Cixi (Alisol(sandy), ca. 4 - 6 m a.s.l) in Zhejiang Province, China. We compared rice paddies with selected neighbouring non-paddy fields and employed AMS 14C as a tool to study C dynamics from bulk, alkali soluble-humic, and insoluble humin samples, and macrofossils (plant remains, charcoal). Our data suggest that vegetation type determines the quantity and quality of biomass introduced as litter and root material in top and subsoil, and thus contributes to the soil C content and profile, which fits the 14C signal distribution, as well as 13C in Ngawi with C4 sugar cane as upland crop. 14C concentrations for the mobile humic acid fraction were generally higher than for bulk samples from the same depth, except when recent plant and root debris led to high 14C levels in near-surface samples. The difference in sampling, - averaged layer for bulk sample and 1-cm layer thickness for point sample - shows gradients in C and 14C across the layers, which could be a reason for discrepancies between the two. High 14C concentrations - in Andosol Sukabumi up to 111 pMC - exceed the atmospheric 14CO2concentration in the sampling year in 2012 (˜ 103 pMC) and

  19. Evaluation of carbon-14 (C{sup 14}) levels of terrestrial and marine food products of the environment of the site of Cogema La Hague; Evaluation des niveaux de carbone-14 ({sup 14}C) des denrees alimentaires terrestres et marines de l'environnement du site de COGEMA - La Hague

    Energy Technology Data Exchange (ETDEWEB)

    NONE

    2006-04-15

    This evaluation has for object to inform about the levels in carbon 14 in the environment of the factories of La Hague. Two sectors were differentiated on one hand the terrestrial environment, and on the other hand the marine environment. The investigations concerned first and foremost food products stemming as the vegetable culture (vegetables) or individual breeding (milk, eggs) but also foodstuffs stemming from the local agriculture (cereal). In touch with the second sector, the marine environment, the sampling concerned the accessible products of the sea by all and those locally marketed (fishes, molluscs, shellfishes). The different results are presented in tables. (N.C.)

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

    Science.gov (United States)

    Hill Bembenic, Meredith A.

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

  1. Contribution of sorption, DOC transport and microbial interactions to the 14C age of a soil organic carbon profile: Insights from a calibrated process model

    NARCIS (Netherlands)

    Ahrens, B.; Braakhekke, M.C.; Guggenberger, G.; Schrumpf, M.; Reichstein, M.

    2015-01-01

    Profiles of soil organic carbon (SOC) are often characterized by a steep increase of 14C age with depth, often leading to subsoil 14C ages of more than 1000 years. These observations have generally been reproduced in SOC models by introducing a SOC pool that decomposes on the time-scale of millennia

  2. A comet could not produce the carbon-14 spike in the 8th century

    CERN Document Server

    Usoskin, Ilya

    2014-01-01

    A mysterious increase of radiocarbon 14C ca. 775 AD in the Earth's atmosphere has been recently found by Miyake et al. (Nature, 486, 240, 2012). A possible source of this event has been discussed widely, the most likely being an extreme solar energetic particle event. A new exotic hypothesis has been presented recently by Liu et al. (Nature Sci. Rep., 4, 3728, 2014) who proposed that the event was caused by a comet bringing additional 14C to Earth. Here we calculated a realistic mass and size of such a comet to show that it would have been huge (~100 km across and 10^{14}-10^{15} ton of mass) and would have produced a disastrous impact on Earth. Such an impact could not remain unnoticed in the geological records and chronicles. The absence of an evidence for such a dramatic event makes this hypothesis invalid.

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

    International Nuclear Information System (INIS)

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

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

    Science.gov (United States)

    Ding, H; Chen, C; Zhang, X

    2016-01-01

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

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

    Science.gov (United States)

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

    2010-03-01

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

  6. Seasonal and snowmelt-driven changes in the water-extractable organic carbon dynamics in a cool-temperate Japanese forest soil, estimated using the bomb-14C tracer

    International Nuclear Information System (INIS)

    Water-extractable organic carbon (WEOC) in soil consists of a mobile and bioavailable portion of the dissolved organic carbon (DOC) pool. WEOC plays an important role in dynamics of soil organic carbon (SOC) and transport of radionuclides in forest soils. Although considerable research has been conducted on the importance of recent litter versus older soil organic matter as WEOC sources in forest soil, a more thorough evaluation of the temporal pattern of WEOC is necessary. We investigated the seasonal variation in WEOC in a Japanese cool-temperate beech forest soil by using the carbon isotopic composition (14C and 13C) of WEOC as a tracer for the carbon sources. Our observations demonstrated that fresh leaf litter DOC significantly contributed to WEOC in May (35–52%) when the spring snowmelt occurred because of the high water flux and low temperature. In the rainy season, increases in the concentration of WEOC and the proportion of hydrophobic compounds were caused by high microbial activity under wetter conditions. From summer to autumn, the WEOC in the mineral soil horizons was also dominated by microbial release from SOC (>90%). These results indicate that the origin and dynamics of WEOC are strongly controlled by seasonal events such as the spring snowmelt and the rainy season's intense rainfall. -- Highlights: • 14C and 13C were used for a tracer for the carbon sources of WEOC in a forest soil. • Fresh leaf litter DOC significantly contributed to WEOC in the spring snowmelt. • Microbial activity caused the increase of WEOC concentration in the rainy season

  7. On the labelling of insuline and insuline derivatives with tritium and carbon-14

    International Nuclear Information System (INIS)

    Two different labelling methods were investigated. By means of the Wilzbach labelling with diaminosuberoylinsuline the insuline is irreversibly altered. As a second method the reductive methylation was used, in doing so it was possible to distinguish between mono and dimethylated parts of the reaction product by using C-14 labelled formaldehyde. Furthermore four N,N-dimethylated insuline derivatives were isolated with yields of 25 until 35%. By using C-14 and h-3 labelled reagents insuline can be labelled doubly. Moreover N-terminal amino groups could be protected irreversibly with this method. Furthermore structure-function investigations and investigations concerning the insuline metabolism were done. (SPI)

  8. Carbon beam extraction with 14.5 GHz electron cyclotron resonance ion source at Korea Atomic Energy Research Institute

    Science.gov (United States)

    Lee, Cheol Ho; Oh, Byung-Hoon; Chang, Dae-Sik; Jeong, Sun-Chan

    2014-02-01

    A 14.5 GHz Electron Cyclotron Resonance ion source (ECRIS) has been made to produce C4+ beam for using a carbon therapy facility and recently tested at KAERI. Highly charged carbon ions have been successfully extracted. When using only CO2 gas, the beam current of C4+ was almost 14 μA at 15 kV extraction voltage. To get higher current of the C4+ beam, while optimizing confinement magnetic field configuration (e.g., axial strengths at minimum and extraction side), gas-mixing (CO2/He), and biased disk were introduced. When the gas mixing ratio of the CO2/He gas is 1:8 at an operational pressure of 5 × 10-7 mbar and the disk was biased to -150 V relative to the ion source body, the highest current of the C4+ beam was achieved to be 50 μA, more than three times higher than previously observed only with CO2 gas. Some details on the operating conditions of the ECRIS were discussed.

  9. Cu Insertion Into the Mo12 Cluster Compound Cs2Mo12Se14: Synthesis, Crystal and Electronic Structures, and Physical Properties.

    Science.gov (United States)

    Al Rahal Al Orabi, Rabih; Fontaine, Bruno; Gautier, Regis; Gougeon, Patrick; Gall, Philippe; Bouyrie, Yohan; Dauscher, Anne; Candolfi, Christophe; Lenoir, Bertrand

    2016-07-01

    Mo-based cluster compounds are promising materials for high-temperature thermoelectric applications due to their intrinsic, extremely low thermal conductivity values. In this study, polycrystalline cluster compounds Cs2CuxMo12Se14 were prepared for a wide range of Cu contents (0 ≤ x ≤ 2). All samples crystallize isostructurally in the trigonal space group R3̅. The position of the Cu atoms in the unit cell was determined by X-ray diffraction on a single-crystalline specimen indicating that these atoms fill the empty space between the Mo-Se clusters. Density functional theory calculations predict a metallic ground state for all compositions, in good agreement with the experimental findings. Magnetization measurements indicate a rapid suppression of the superconducting state that develops in the x = 0.0 sample upon Cu insertion. Transport properties measurements, performed in a wide temperature range (2-630 K) on the two end-member compounds x = 0 and x = 2, revealed a multiband electrical conduction as shown by sign reversal of the thermopower as a function of temperature. PMID:27304903

  10. Carbon-14 based determination of the biogenic fraction of industrial CO2 emissions : Application and validation

    NARCIS (Netherlands)

    Palstra, S. W. L.; Meijer, H. A. J.

    2010-01-01

    The C-14 method is a very reliable and sensitive method for industrial plants, emission authorities and emission inventories to verify data estimations of biogenic fractions of CO2 emissions. The applicability of the method is shown for flue gas CO2 samples that have been sampled in I-h intervals at

  11. Carbon-14 labelled nitrogen heterocycles; the syntheses of three phosphodiesterase inhibitors

    International Nuclear Information System (INIS)

    The syntheses of three heterocyclic phosphodiesterase inhibitors are described from a common radiolabelled precursor, namely 2-propoxybenzo[cyano-14C] nitrile. Conversion of the nitrile to the corresponding methyl ketone or amidine allows elaboration of the heterocycles radiolabelled within the ring systems. (Author)

  12. Constraints on emissions of carbon monoxide, methane, and a suite of hydrocarbons in the Colorado Front Range using observations of 14CO2

    OpenAIRE

    LaFranchi, B. W; Pétron, G.; Miller, J. B.; S. J. Lehman; Andrews, A. E; E. J. Dlugokencky; Hall, B.; Miller, B. R.; Montzka, S. A.; W. Neff; P. C. Novelli; C. Sweeney; J. C. Turnbull; D. E. Wolfe; P. P. Tans

    2013-01-01

    Atmospheric radiocarbon (14C) represents an important observational constraint on emissions of fossil-fuel derived carbon into the atmosphere due to the absence of 14C in fossil fuel reservoirs. The high sensitivity and precision that accelerator mass spectrometry (AMS) affords in atmospheric 14C analysis has greatly increased the potential for using such measurements to evaluate bottom-up emissions inventories of fossil fuel CO2 (CO2ff), as well as those for other co-emitte...

  13. Interactive effects between carbon allotropes on the mechanical reinforcement of nanocomposites based on poly(1,4-cis-isoprene)

    Science.gov (United States)

    Musto, Sara; Cipolletti, Valeria; Barbera, Vincenzina; Agnelli, Silvia; Pandini, Stefano; Galimberti, Maurizio

    2014-05-01

    Interactive effects of carbon allotropes on the mechanical reinforcement of polymer nanocomposites were investigated by using, as the polymer matrix, poly(1,4-cis-isoprene) (PI) samples from industrial synthesis and from natural sources. Carbon nanotubes (CNT) and nano-graphite with high shape anisotropy (nanoG) were melt blended with PI, as the only fillers or in combination with carbon black (CB), measuring the shear modulus at low strain amplitudes. The nanofiller was found to increase the low amplitude storage modulus of the matrix, with or without CB, by a factor depending on nanofiller type and content. The filler-polymer interfacial area was able to correlate modulus data of composites with CNT, CB and with the hybrid filler system, leading to the construction of a common master curve. The filler networking phenomenon was found to be affected by type and amount of low molecular mass products of PI from natural sources. The correlation between chemical composition, dynamic mechanical and ultimate properties of nanocomposites was investigated. In particular, it was found that low molecular mass components control the ability of elastomeric nano-composites to store or dissipate energy.

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

    Energy Technology Data Exchange (ETDEWEB)

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

    2007-07-01

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

  15. Coupling granular activated carbon adsorption with membrane bioreactor treatment for trace organic contaminant removal: breakthrough behaviour of persistent and hydrophilic compounds.

    Science.gov (United States)

    Nguyen, Luong N; Hai, Faisal I; Kang, Jinguo; Price, William E; Nghiem, Long D

    2013-04-15

    This study investigated the removal of trace organic contaminants by a combined membrane bioreactor - granular activated carbon (MBR-GAC) system over a period of 196 days. Of the 22 compounds investigated here, all six hydrophilic compounds with electron-withdrawing functional groups (i.e., metronidazole, carbamazepine, ketoprofen, naproxen, fenoprop and diclofenac) exhibited very low removal efficiency by MBR-only treatment. GAC post-treatment initially complemented MBR treatment very well; however, a compound-specific gradual deterioration of the removal of the above-mentioned problematic compounds was noted. While a 20% breakthrough of all four negatively charged compounds namely ketoprofen, naproxen, fenoprop and diclofenac occurred within 1000-3000 bed volumes (BV), the same level of breakthrough of the two neutral compounds metronidazole and carbamazepine did not occur until 11,000 BV. Single-solute isotherm parameters did not demonstrate any discernible correlation individually with any of the parameters that may govern adsorption onto GAC, such as log D, number of hydrogen-bond donor/acceptor groups, dipole moment or aromaticity ratio of the compounds. The isotherm data, however, could differentiate the breakthrough behaviour between negatively charged and neutral trace organic contaminants.

  16. Characterization of airborne particulates by pyrolysis/mass spectrometry and carbon-14 analysis

    Energy Technology Data Exchange (ETDEWEB)

    Voorhees, K.J. (Colorado School of Mines, Golden); Durfee, S.L.; Currie, L.A.; Klouda, G.A.

    1981-08-01

    Pyrolysis/mass spectrometry (Py/MS) has been used to characterize the composition of organics in an ambient air particulate sample from the eastern Utah oil shale lands. The procedure involved collection of the individual contributors, pyrolysis of these samples, and finally a least-squares fitting of the individual contributor spectra to the pyrolysis mass spectrum of the ambient sample. The Py/MS results were verified by using /sup 14/C analysis.

  17. Effects of entrainment through Oconee Nuclear Station on carbon-14 assimilation rates of phytoplankton

    International Nuclear Information System (INIS)

    Carbon assimilation rates of phytoplankton communities entrained through Oconee Nuclear Station were measured on six dates during 1974. Thermal, mechanical, condenser, and multiple entrainment effects on uptake rates were compared by incubating samples in vitro in controlled-temperature water baths. Duplicate light and dark bottles containing water from four cooling-system locations were exposed to temperatures approximating intake and discharge temperatures. The relationships were variable, but exposure of the hypolimnetic intake water at near-discharge temperatures (thermal effect) stimulated primary productivity in four of six experiments. Multiple entrainment and mechanical effects caused no consistent change in assimilation rates

  18. Design, synthesis, and biological evaluation of 1,2,3-trisubstituted-1,4-dihydrobenzo[g]quinoxaline-5,10-diones and related compounds as antifungal and antibacterial agents.

    Science.gov (United States)

    Tandon, Vishnu K; Yadav, Dharmendra B; Maurya, Hardesh K; Chaturvedi, Ashok K; Shukla, Praveen K

    2006-09-01

    A series of (S)-N-(3-chloro-1,4-naphthoquinon-2-yl)-alpha-amino acid ethyl esters 3 and 1,2,3-trisubstituted-1,4-dihydrobenzo[g]quinoxaline-5,10-diones 6-23 were synthesized and evaluated for antifungal and antibacterial activities. The structure-activity relationship of these compounds was studied and the results show that the compounds 3a and 3b exhibited in vitro antifungal activity against Candida albicans, Cryptococcus neoformans, and Sporothrix schenckii whereas compounds 12 and 22 showed in vitro antibacterial activity against Klebsiella pneumoniae and Escherichia coli.

  19. Interaction of pinaverium (a quaternary ammonium compound) with 1,4-dihydropyridine binding sites in rat ileum smooth muscle.

    Science.gov (United States)

    Feron, O; Wibo, M; Christen, M O; Godfraind, T

    1992-02-01

    1. The interaction of pinaverium bromide, a quaternary ammonium compound, with binding sites for (L-type) calcium channel blockers was investigated in rat ileum smooth muscle. 2. Pinaverium inhibited [3H]-(+)-PN200-110 ([3H]-(+)-isradipine) specific binding to tissue homogenates incompletely (Ki 0.38 microM; maximal inhibition 80%). In contrast, binding to single cell preparations (obtained by collagenase treatment) and to saponin-treated homogenates was completely inhibited. These data are compatible with the view that, in untreated homogenates, 20% of [3H]-(+)-isradipine binding sites are not accessible to pinaverium because it is associated with sealed inside-out vesicles. 3. Pinaverium bromide increased the apparent KD of [3H]-(+)-isradipine binding to saponin-treated homogenates but did not significantly affect the Bmax value. Moreover, the dissociation rate constant of [3H]-(+)-isradipine binding was not changed by pinaverium. These data suggest that pinaverium interacts with the dihydropyridine binding site in a competitive manner. However, in contrast to uncharged dihydropyridine calcium antagonists, pinaverium inhibited, rather than stimulated, [3H]-diltiazem binding to rat brain membranes (at 30-37 degrees C). 4. Although Bmax values of [3H]-(+)-isradipine were similar in homogenates prepared from tissue and cells (collagenase-treated), the KD value was significantly higher in cell homogenates (166 vs 95 pM). Similarly, the Ki value of pinaverium was higher in cell preparations than in tissue homogenates (0.77 vs 0.38 microM). Thus, collagenase can significantly modify the dihydropyridine recognition site.5. The competitive interaction of pinaverium, a permanently charged drug, with [3H]-(+)-isradipine bound to intact cells and its absence of interaction with [3H]-(+)-isradipine bound to sealed inside-out vesicles imply that the dihydropyridine receptor lies near the external surface of the plasma membrane. PMID:1313732

  20. Enhanced Product Recovery from Glycerol Fermentation into 3-Carbon Compounds in a Bioelectrochemical System Combined with In Situ Extraction

    Science.gov (United States)

    Roume, Hugo; Arends, Jan B. A.; Ameril, Camar P.; Patil, Sunil A.; Rabaey, Korneel

    2016-01-01

    Given the large amount of crude glycerol formed as a by-product in the biodiesel industries and the concomitant decrease in its overall market price, there is a need to add extra value to this biorefinery side stream. Upgrading can be achieved by new biotechnologies dealing with recovery and conversion of glycerol present in wastewaters into value-added products, aiming at a zero-waste policy and developing an economically viable process. In microbial bioelectrochemical systems (BESs), the mixed microbial community growing on the cathode can convert glycerol reductively to 1,3-propanediol (1,3-PDO). However, the product yield is rather limited in BESs compared with classic fermentation processes, and the synthesis of side-products, resulting from oxidation of glycerol, such as organic acids, represents a major burden for recovery of 1,3-PDO. Here, we show that the use of an enriched mixed-microbial community of glycerol degraders and in situ extraction of organic acids positively impacts 1,3-PDO yield and allows additional recovery of propionate from glycerol. We report the highest production yield achieved (0.72 mol1,3-PDO mol−1glycerol) in electricity-driven 1,3-PDO biosynthesis from raw glycerol, which is very close to the 1,3-PDO yield reported thus far for a mixed-microbial culture-based glycerol fermentation process. We also present a combined approach for 1,3-PDO production and propionate extraction in a single three chamber reactor system, which leads to recovery of additional 3-carbon compounds in BESs. This opens up further opportunities for an economical upgrading of biodiesel refinery side or waste streams. PMID:27725929

  1. Elimination of hydrophobic volatile organic compounds in fungal biofilters: reducing start-up time using different carbon sources.

    Science.gov (United States)

    Vergara-Fernández, Alberto; Hernández, Sergio; Revah, Sergio

    2011-04-01

    Fungal biofilters have been recently studied as an alternative to the bacterial systems for the elimination of hydrophobic volatile organic compounds (VOC). Fungi foster reduced transport limitation of hydrophobic VOCs due to their hydrophobic surface and extended gas exchange area associated to the hyphal growth. Nevertheless, one of their principal drawbacks is their slow growth, which is critical in the start-up of fungal biofilters. This work compares the use of different carbon sources (glycerol, 1-hexanol, wheat bran, and n-hexane) to reduce the start-up period and sustain high n-hexane elimination capacities (EC) in biofilters inoculated with Fusarium solani. Four parallel experiments were performed with the different media and the EC, the n-hexane partition coefficient, the biomass production and the specific consumption rate were evaluated. Biofilters were operated with a residence time of 1.3 min and an inlet n-hexane load of 325 g m(-3) (reactor) h(-1). The time to attain maximum EC once gaseous n-hexane was fed was reduced in the three experiments with alternate substrates, as compared to the 36 days needed with the control where only n-hexane was added. The shortest adaptation period was 7 days when wheat bran was initially used obtaining a maximum EC of 160 g m(-3) (reactor) h(-1) and a critical load of 55 g m(-3) (reactor) h(-1). The results were also consistent with the pressure drop, the amount of biomass produced and its affinity for the gaseous n-hexane, as represented by its partition coefficient.

  2. A novel carbon-14 'solvent-free'-labeling procedure with diethyl malonate

    International Nuclear Information System (INIS)

    A novel labelling procedure for dialkyl malonate preparation under 'solvent-free' conditions in the presence of a phase transfer catalyst was developed. Improved radiochemical yields (about 70%) as compared to the classical preparation routes in DMF are achieved in mere 10 minutes at 130 deg C. General labelling procedures for alkyl bromides are reported. The radiochemical purity by HPLC and analysis conditions using online radioactivity detection are described. The preparation of radiochemicals by this method shows major advantages as regards the purification of the final labelled compound and, since no organic solvent is used, waste management. A simple and easy two-step chromatographic procedure gives rise to pure dialkyl malonates. The method can be especially useful in short-lived isotope labelling

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

    Institute of Scientific and Technical Information of China (English)

    2001-01-01

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

  4. Carbon-14 ages of Antarctic meteorites with accelerator and small-volume counting techniques

    International Nuclear Information System (INIS)

    C-14 measurements were made on six Yamato and Victoria Land meteorites using tandem accelerator mass spectroscopy. The studies brought to 27 the number of Antarctic meteorites that have been examined for terrestrial aging. Details of the spectroscopic method are provided, along with the results in combinations with the data from the other 21 meteorites. It is found that the Yamato meteorites are younger than those found at Allan Hills, implying that two mechanisms may exist for the abundant Antarctic meteorites: exposure where falling due to a paucity of ice, and transport and exposure by sublimating ice

  5. Age determination of ground-waters by means of carbon 14

    International Nuclear Information System (INIS)

    At present the age determination of ground-waters aged between 1,500 and approximately 40,000 years is only possible by measuring their 14C content. A precise age assignment can be established in slightly mineralised waters, whereas it becomes vague in mineralised waters, particularly in acidulous springs. In general, additional information and data are required about the 13C, D, 18O, 3H, 85Kr and the 39Ar contents, about the ph value, temperature and the principal ions. (DG)

  6. Carbon Nanotube and Nanofiber Exposure Assessments: An Analysis of 14 Site Visits.

    Science.gov (United States)

    Dahm, Matthew M; Schubauer-Berigan, Mary K; Evans, Douglas E; Birch, M Eileen; Fernback, Joseph E; Deddens, James A

    2015-07-01

    Recent evidence has suggested the potential for wide-ranging health effects that could result from exposure to carbon nanotubes (CNT) and carbon nanofibers (CNF). In response, the National Institute for Occupational Safety and Health (NIOSH) set a recommended exposure limit (REL) for CNT and CNF: 1 µg m(-3) as an 8-h time weighted average (TWA) of elemental carbon (EC) for the respirable size fraction. The purpose of this study was to conduct an industrywide exposure assessment among US CNT and CNF manufacturers and users. Fourteen total sites were visited to assess exposures to CNT (13 sites) and CNF (1 site). Personal breathing zone (PBZ) and area samples were collected for both the inhalable and respirable mass concentration of EC, using NIOSH Method 5040. Inhalable PBZ samples were collected at nine sites while at the remaining five sites both respirable and inhalable PBZ samples were collected side-by-side. Transmission electron microscopy (TEM) PBZ and area samples were also collected at the inhalable size fraction and analyzed to quantify and size CNT and CNF agglomerate and fibrous exposures. Respirable EC PBZ concentrations ranged from 0.02 to 2.94 µg m(-3) with a geometric mean (GM) of 0.34 µg m(-3) and an 8-h TWA of 0.16 µg m(-3). PBZ samples at the inhalable size fraction for EC ranged from 0.01 to 79.57 µg m(-3) with a GM of 1.21 µg m(-3). PBZ samples analyzed by TEM showed concentrations ranging from 0.0001 to 1.613 CNT or CNF-structures per cm(3) with a GM of 0.008 and an 8-h TWA concentration of 0.003. The most common CNT structure sizes were found to be larger agglomerates in the 2-5 µm range as well as agglomerates >5 µm. A statistically significant correlation was observed between the inhalable samples for the mass of EC and structure counts by TEM (Spearman ρ = 0.39, P 1 μg m(-3). Until more information is known about health effects associated with larger agglomerates, it seems prudent to assess worker exposure to airborne CNT and CNF

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

    Energy Technology Data Exchange (ETDEWEB)

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

    2003-03-01

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

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

    Science.gov (United States)

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

    2013-05-01

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

  9. AccR is a master regulator involved in carbon catabolite repression of the anaerobic catabolism of aromatic compounds in azoarcus sp. CIB

    OpenAIRE

    Valderrama, J. Andrés; Shingler, Victoria; Carmona Pérez, Manuel; Díaz, Eduardo

    2013-01-01

    Background: Mechanisms underlying carbon catabolite repression (CCR) control of the anaerobic degradation of aromatic compounds have previously remained elusive. Results: Phosphorylated AccR was identified as a transcriptional repressor of aromatic degradation operons expressed under anaerobic conditions. Conclusion: The response regulator AccR controls the succinate-dependent CCR in Azoarcus sp. CIB. Significance: AccR is a master regulator that controls anaerobic CCR in bacteria. © 2014 by ...

  10. Paleo-vegetation study using dating by 14 C and carbon isotope ratio

    International Nuclear Information System (INIS)

    Different approaches that include biological, geomorphological and botanical studies have been used to infer past climatic changes in the Amazon. Our approach involve the use of 13 C analyses in soil organic matter to infer past vegetation changes based on distinct isotopic composition that characterize C3 and C4 plants, and 14 C is used as dating tool, in two regions of natural Forest and Cerrado, located in Rondonia state. The soil at the Forest site is Podzolico Vermelho Amarelo and the Cerrado site is a Latosol Vermelho Amarelo. Radiocarbon analyses of total soil fraction samples indicate that the organic matter in these soils is at least Holocene in age δ13 C values for total soil organic matter in the forest varies from-28 at the surface to 25% at depth of 2 m, indicating the predominance of a C3 cycle in the last 3 270 yrs. At the Cerrado the δ13 C change from -21 to -14% in the first 30 cm characterizing C4 cycle and changed to -19% at 135 cm, probably characterizing a mixture between C3 and C4 plants and an increase to -16% is observed at 195 cm, again indicating a predominance of C4 plants. This data show that the Cerrado ecosystem was much more dynamics in term of vegetation changes than Forest. (author). 10 refs, 2 figs, 1 tab

  11. Enzymatic determination of carbon-14 labeled L-alanine in biological samples

    International Nuclear Information System (INIS)

    A method for determination of L-alanine-specific radioactivity in biological samples is presented. This method is based on the specific enzymatic transformation of L-alanine to pyruvic acid hydrazone catalyzed by the enzyme L-alanine dehydrogenase, formation of the pyruvic acid 2,4-dinitrophenylhydrazone derivative, and quantitative trapping in Amberlite XAD-7 columns, followed by radioactivity counting of the lipophilic eluate. No interferences from other 14C-labeled materials such as D-glucose, glycerol, L-lactate, L-serine, L-glutamate, L-phenylalanine, glycine, L-leucine, and L-arginine were observed. This inexpensive and high-speed method is applicable to the simultaneous determination of L-alanine-specific radioactivity for a large number of samples

  12. Partitioning sources of recharge in environments with groundwater recirculation using carbon-14 and CFC-12

    Science.gov (United States)

    Bourke, Sarah A.; Cook, Peter G.; Dogramaci, Shawan; Kipfer, Rolf

    2015-06-01

    Groundwater recirculation occurs when groundwater is pumped from an aquifer onto the land surface, and a portion of that water subsequently infiltrates back to the aquifer. In environments where groundwater is recirculated, differentiation between various sources of recharge (e.g. natural rainfall recharge vs. recirculated water) can be difficult. Groundwater age indicators, in particular transient trace gases, are likely to be more sensitive tracers of recharge than stable isotopes or chloride in this setting. This is because, unlike stable isotopes or chloride, they undergo a process of equilibration with the atmosphere, and historical atmospheric concentrations are known. In this paper, groundwater age indicators (14C and CFC-12) were used as tracers of recharge by surplus mine water that is discharged to streams. Ternary mixing ratios were calculated based on 14C and CFC-12 concentrations measured along three transects of piezometers and monitoring wells perpendicular to the creeks, and from dewatering wells. Uncertainty in calculated mixing ratios was estimated using a Monte Carlo approach. Ternary mixing ratios in dewatering wells suggest that recharge by mine water accounted for between 10% and 87% of water currently abstracted by dewatering wells. The calculated mixing ratios suggest that recharge by mine water extends to a distance of more than 550 m from the creeks. These results are supported by seepage flux estimates based on the water and chloride balance along the creeks, which suggest that 85-90% of mine water discharged to the creeks recharges the aquifer and recharge by mine water extends between 110 and 730 m from the creeks. Mixing calculations based on gaseous groundwater age indicators could also be used to partition recharge associated with agricultural irrigation or artificial wetland supplementation.

  13. Content of peroxide compounds and 14C-leucine incorporation in subcellular fractions of new embryos obtained from poultry fed with antioxidants

    International Nuclear Information System (INIS)

    The formation of peroxide compounds in feed mixtures and the poultry organism was investigated. Two groups of broilers were fed with whole fodder mixture. The controls received a basic diet, while the experimental group got in addition 125 ppm each of the ethoxyquin antioxidant. 14C leucine was applied to the 14-day embryos in the eggs air space in a 20 microcurie dose per embryo. The incorporation of the labelled precursor was determined on the 3rd hour after introduction of the isotope. The radiometric analysis was made by the filter method with a liquid scintillation counter. The relative distribution of labelled leucine in the liver subcellular fractions of the control embryos revealed a pattern characteristic of their protein synthesizing capacity. The relative distribution of the labelled precursor in the experimental group showed the same pattern. The greater precursor incorporation in the nuclei of the embryos in the experimental group, however, suggests that ethoxyquin might stimulate nuclear protein synthesis or the passage of more protein from the cytoplasm, which is then utilized by the nucleolus for the development of the ribosomal apparatus

  14. Light-driven increase in carbon yield is linked to maintenance in the proteorhodopsin-containing Photobacterium angustum S14

    Directory of Open Access Journals (Sweden)

    Alicia eCourties

    2015-07-01

    Full Text Available A type of photoheterotrophic bacteria contain a transmembrane light-driven proton pump called proteorhodopsins (PRs. Due to the prevalence of these organisms in the upper water column of the World’s Ocean, and their potential for light driven ATP generation, they have been suggested to significantly influence energy and matter flows in the biosphere. To date, evidence for the significance of the light-driven metabolism of PR-containing prokaryotes has been obtained by comparing growth in batch culture, under light versus dark conditions, and it appears that responses to light are linked to unfavorable conditions, which so far have not been well parameterized. We studied light responses to carbon yields of the PR-containing Photobacterium angustum S14 using continuous culture conditions and light-dark cycles. We observed significant effects of light-dark cycles compared to dark controls, as well as significant differences between samples after 12 h illumination versus 12 h darkness. However these effects were only observed under higher cell counts and lower pH associated with higher substrate concentrations. Under these substrate levels Pirt’s maintenance coefficient was higher when compared to lower substrate dark controls, and decreased under light-dark cycles. It appears that light responses by Photobacterium angustum S14 are induced by the energetic status of the cells rather than by low substrate concentrations.

  15. Catalytic hydrogenation of carbon monoxide. Progress report, December 15, 1991--December 14, 1992

    Energy Technology Data Exchange (ETDEWEB)

    Wayland, B.B.

    1992-12-01

    This project is focused on developing strategies to accomplish the reduction and hydrogenation of carbon monoxide to produce organic oxygenates at mild conditions. Our approaches to this issue are based on the recognition that rhodium macrocycles have unusually favorable thermodynamic values for producing a series of intermediate implicated in the catalytic hydrogenation of CO. Observations of metalloformyl complexes produced by reactions of H{sub 2} and CO, and reductive coupling of CO to form metallo {alpha}-diketone species have suggested a multiplicity of routes to organic oxygenates that utilize these species as intermediates. Thermodynamic and kinetic-mechanistic studies are used in constructing energy profiles for a variety of potential pathways, and these schemes are used in guiding the design of new metallospecies to improve the thermodynamic and kinetic factors for individual steps in the overall process. Variation of the electronic and steric effects associated with the ligand arrays along with the influences of the reaction medium provide the chemical tools for tuning these factors. Emerging knowledge of the factors that contribute to M-H, M-C and M-O bond enthalpies is directing the search for ligand arrays that will expand the range of metal species that have favorable thermodynamic parameters to produce the primary intermediates for CO hydrogenation. Studies of rhodium complexes are being extended to non-macrocyclic ligand complexes that emulate the favorable thermodynamic features associated with rhodium macrocycles, but that also manifest improved reaction kinetics. Multifunctional catalyst systems designed to couple the ability of rhodium complexes to produce formyl and diketone intermediates with a second catalyst that hydrogenates these imtermediates are promising approaches to accomplish CO hydrogenation at mild conditions.

  16. Metabolism and distribution of 14C- and 35S-labeled carbon disulfide in immature rats of different ages

    International Nuclear Information System (INIS)

    The metabolism and distribution of 14C- and 35S-CS2 was examined in 1-, 5-, 10-, 20-, 30-, and 40-day-old rats. During a 3-hr period following an ip dose of 14C-CS2, 58-83% of the dose was expired as CS2 and 4-9% was metabolized to expired CO2 depending on age. Thirty- and forty-day-old rats metabolized significantly more CS2 to CO2 and expired significantly less CS2 than 1- through 20-day-old rats. At the end of the measured expiration period, only biotransformation products of CS2, which were in part covalently bound, remained in tissues from rats of all ages. Tissue levels of 35S-CS2-derived radioactivity exceeded levels of 14C-CS2-derived radioactivity indicating that sulfur metabolites free from the carbon atom of CS2 were formed in rats as young as 1 day of age. The 35S-CS2-derived radioactivity per g of tissue and thus 35S covalently bound to tissue protein was significantly higher in 1- through 20-day-old rats than in 30- and 40-day-old rats. Twenty-four hr after dosing, up to 13 times more 35S-labeled metabolites were covalently bound in organs from 1-day-old rats than in similar organs from 40-day-old rats. The results showed that elimination of the biotransformation products of CS2, in particular the covalently binding sulfur metabolites, was prolonged in newborn rats in comparison to 40-day-old rats

  17. Soil aggregate fraction-based 14C analysis and its application in the study of soil organic carbon turnover under forests of different ages

    Institute of Scientific and Technical Information of China (English)

    TAN WenBing; ZHOU LiPing; LIU KeXin

    2013-01-01

    There still exist uncertainties in the trend,magnitude and efficiency of carbon sequestration with regard to the changes in soil organic carbon (SOC) pools after afforestation.In this study,SOC turnover times of the meadow steppe and planted forests at Saihanba Forest Station of Hebei Province,China are estimated by means of the radiocarbon (14C) method.Our results show that the SOC turnover times can be as long as from 70 to 250 years.After planting the Pinus sylvestri var.mongolica in the Leymus chinensis meadow steppe,the turnover times of organic carbon in both bulk samples and soil aggregate fractions of the topsoils are decreased with an increase of the stand age.Such a lowering of the turnover time would cause an increase in soil CO2 flux,implying that afforestation of grassland may reduce the capacity of topsoil to sequestrate organic carbon.Combined stable isotope and 14C analyses on soil aggregate fractions suggest that there are different responses to afforestation of grassland between young and old carbon pools in topsoils.In the young and middle-age planted forests,the proportion of CO2 emission from the older soil carbon pool shows an increasing trend.But in the mature planted forest,its proportion tends to decline,indicating that the stand age may influence the soil carbon sequestration mechanism.The CO2 emission from the topsoils estimated using the 14C method is relatively low compared to those by other methods and may be caused by the partial isolation of the young carbon component from the soil aggregates.For more accurate estimation of CO2 flux,future studies should therefore employ improved methodology for more effective separation of different soil carbon components before isotope analyses.

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

    Science.gov (United States)

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

    2016-09-01

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

  19. Carbon-14 transfer into potato plants following a short exposure to an atmospheric 14CO2 emission: observations and model predictions.

    Science.gov (United States)

    Melintescu, A; Galeriu, D; Tucker, S; Kennedy, P; Siclet, F; Yamamoto, K; Uchida, S

    2013-01-01

    To improve the understanding of the environmental (14)C behaviour, the International Atomic Energy Agency (IAEA) coordinated a Tritium and C-14 Working Group (T&C WG) in its EMRAS (Environmental Modelling for Radiation Safety) programme. One of the scenarios developed in the frame of T&C WG involved the prediction of time dependent (14)C concentrations in potato plants. The experimental data used in the scenario were obtained from a study in which potatoes (Solanum tuberosum cv. Romano) were exposed to atmospheric (14)CO(2) in a wind tunnel. The observations were used to test models that predict temporal changes in (14)C concentrations in leaves at each sampling time for each experiment and (14)C concentrations in tubers at the final harvest of each experiment. The experimental data on (14)C dynamics in leaves are poorly reproduced by most of the models, but the predicted concentrations in tubers are in good agreement with the observations. PMID:22995861

  20. Nuclear graphite waste's behaviour under disposal conditions: Study of the release and repartition of organic and inorganic forms of carbon 14 and tritium in alkaline media

    International Nuclear Information System (INIS)

    23000 tons of graphite wastes will be generated during dismantling of the first generation of French reactors (9 gas cooled reactors). These wastes are classified as Long Lived Low Level wastes (LLW-LL). As requested by the law, the French National Radioactive Waste Management Agency (Andra) is studying concepts of low-depth disposals.In this work we focus on carbon 14, the main long-lived radionuclide in graphite waste (5730 y), but also on tritium, which is the main contributor to the radioactivity in the short term. Carbon 14 and tritium may be released from graphite waste in many forms in gaseous phase (14CO2, HT...) or in solution (14CO32-, HTO...). Their speciation will strongly affect their migration from the disposal site to the environment. Leaching experiments, in alkaline solution (0.1 M NaOH simulating repository conditions) have been performed on irradiated graphite, from Saint-Laurent A2 and G2 reactors, in order to quantify their release and characterize their speciation. The studies show that carbon 14 exists in both gaseous and aqueous phases. In the gaseous phase, release is weak (≤0.1%) and corresponds to oxidizable species. Carbon 14 is mainly released into liquid phase, as both inorganic and organic species. 65% of released fraction is inorganic and 35% organic carbon. Two tritiated species have been identified in gaseous phase: HTO and HT/Organically Bond Tritium. More than 90% of tritium in that phase corresponds to HT/OBT. But release is weak (≤0.1%). HTO is mainly in the liquid phase. (author)

  1. Compound specific isotopic fractionation patterns suggest different carbon metabolisms among Chloroflexus-like bacteria in hot spring microbial mats

    NARCIS (Netherlands)

    Sinninghe Damsté, J.S.; Meer, M.T.J. van der; Schouten, S.; Leeuw, J.W. de; Ward, D.M.

    2003-01-01

    Stable carbon isotope fractionations between dissolved inorganic carbon and lipid biomarkers suggest photoautotrophy by Chloroflexus-like organisms in sulfidic and nonsulfidic Yellowstone hot springs. Where co-occurring, cyanobacteria appear to cross-feed Chloroflexus-like organisms supporting photo

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

    Energy Technology Data Exchange (ETDEWEB)

    Perez-Garcia, M. M.

    1972-07-01

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

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

    Science.gov (United States)

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

    2016-08-01

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

  4. Peculiarities in aromatization mechanism of low-molecular aliphatic compounds over high-silica zeolites

    Energy Technology Data Exchange (ETDEWEB)

    Isagulyants, G.V.; Gitis, K.M.; Dubinskij, Yu.G.; Timokhov, A.G.; Kornyshev, V.N. (AN SSSR, Moscow. Inst. Organicheskoj Khimii)

    1984-01-01

    By means of /sup 14/C labelled compounds, transformations of methanol, lower olefins and piperylene over high-silica zeolites the data on the mechanism of carbon sceleton growth in the course of olefins production from methanol and aromatic piperylene hydrocarbons are obtained. Compound transformations have been studied at the pulse microcatalytic installation with radiochromatographic analysis of products.

  5. Influence of Carbon Black on the Heat Aging Properties of Rubber Compounds%炭黑对橡胶耐热老化性能的影响

    Institute of Scientific and Technical Information of China (English)

    柴克鹏; 沈惠玲

    2015-01-01

    研究炭黑对橡胶耐热老化性能的影响。结果表明:在炭黑结构相同的条件下,随着炭黑粒径增大,胶料的门尼粘度减小,强伸性能降低,耐热老化性能提高;通过并用耐热老化性能好的炭黑可以改善胶料的耐热老化性能。%In this study, the inlfuence of carbon black on the heat aging properties of rubber compounds was investigated. The experimental test results showed that, when the carbon black has similar structure and the particle size increased, the Mooney viscosity of the compound was reduced, the tensile properties of the vulcanizates decreased and the heat ageing properties were improved. It was found that with combination of different carbon black with good heat ageing properties, the heat ageing properties of the vulcanizates were improved.

  6. The crystal structure and physicochemical characteristics of 2-hydroxy-N-[3(5)-pyrazolyl]-1,4-naphthoquinone-4-imine, a new antitrypanosomal compound.

    Science.gov (United States)

    Sperandeo, Norma R; Karlsson, Alicia; Cuffini, Silvia; Pagola, Silvina; Stephens, Peter W

    2005-01-01

    This study was designed to investigate the physical characteristics and crystalline structure of 2-hydroxy-N-[3(5)-pyrazolyl]-1,4-naphthoquinone-4-imine (PNQ), a new active compound against Trypanosoma cruzi, the causative agent of American trypanosomiasis. Methods used included differential scanning calorimetry, thermogravimetry, hot stage microscopy, polarized light microscopy (PLM), Fourier-transform infrared (FTIR) spectroscopy, and high-resolution X-ray powder diffraction (HR-XRPD). According to PLM and HR-XRPD data, PNQ crystallized as red oolitic crystals (absolute methanol) or prisms (dimethyl sulfoxide [DMSO]-water) with the same internal structure. The findings obtained with HR-XRPD data (applying molecular location methods) showed a monoclinic unit cell [a = 18.4437(1) A, b = 3.9968(2) A, c = 14.5304(1) A, alpha = 90 degrees , beta = 102.71(6) degrees , gamma = 90 degrees , V = 1044.9(1) A(3), Z = 4, space group P2(1)/c], and a crystal structure (excluding H-positions) described by parallel layers in the direction of the b-axis, with molecules held by homochemical (phenyl-phenyl and pyrazole-pyrazole) van der Waals interactions. In addition, FTIR spectra displayed the NH-pyrazole stretch overlapped with the OH absorption at 3222 cm(-1), typical of -NH and -OH groups associated through H-bondings; and a carbonyl stretching absorption at 1694 cm(-1), indicating a nonextensively H-bonded quinonic C=O, which was in accordance with the solved crystal structure of PNQ. The existence of such cohesive forces shed light on the thermoanalytical data, which revealed that PNQ is a stable solid, unaffected by oxygen that decomposed without melting above 260 degrees C. PMID:16408868

  7. Ventilation of the deep Greenland and Norwegian seas: evidence from krypton-85, tritium, carbon-14 and argon-39

    International Nuclear Information System (INIS)

    On leg 5 of the TTO expedition, the distributions of 85Kr, tritium, 14C, 39Ar, temperature, salinity, oxygen, carbon dioxide and nutrients were measured in the Greenland and Norwegian seas. These observations support previous observations that Greenland Sea Deep Water is formed by a deep convective process within the Greenland gyre. They also support AAGAARD et al.'s (1985, Journal of Geophysical Research, 90, 4833-4846) new hypothesis that Norwegian Sea Deep Water forms from a mixture of Greenland Sea Deep Water and Eurasian Basin Deep Water. Volume transports estimated from the distributions of 85Kr, tritium, 14C and 39Ar range from 0.53 to 0.74 Sv for exchange between the surface and deep Greenland Sea and from 0.9 to 1.47 Sv for exchange between the deep Greenland and deep Norwegian Seas. The residence time of water and the deep Greenland Sea with respect to exchange with surface water ranges from 24 to 34 years reported by PETERSON and ROOTH (1976, Deep-Sea Research, 23, 273-283) and 35-42 years reported by BULLISTER and WEISS (1983, Science, 221, 265-268). The residence time of water in the deep Norwegian Sea with respect to exchange with the deep Greenland Sea ranges from 19 to 30 years compared to 97-107 years reported by PETERSON and ROOTH (1976) and 10-28 years reported by BULLISTER and WEISS (1983). The oxygen consumption rate was estimated to be at most 1.04 μM kg-1 y-1 for the deep Greenland Sea and to be between 0.47 and 0.79 μM kg-1 y-1 for the deep Norwegian Sea. (author)

  8. In situ carbon and nitrogen dynamics in ryegrass-clover mixtures

    DEFF Research Database (Denmark)

    Rasmussen, J.; Eriksen, J.; Jensen, Erik Steen;

    2007-01-01

    =9). 15N-enriched compounds were not detected in percolating pore water, which may be caused by either dilution from irrigation or low availability of leachable N compounds. 14C was found solely as 14CO2 in the pore water indicating that dissolved organic carbon (DOC) did not originate from fresh...

  9. Accuracy and precision of 14C-based source apportionment of organic and elemental carbon in aerosols using the Swiss_4S protocol

    Directory of Open Access Journals (Sweden)

    G. O. Mouteva

    2015-04-01

    Full Text Available Aerosol source apportionment remains a critical challenge for understanding the transport and aging of aerosols, as well as for developing successful air pollution mitigation strategies. The contributions of fossil and non-fossil sources to organic carbon (OC and elemental carbon (EC in carbonaceous aerosols can be quantified by measuring the radiocarbon (14C content of each carbon fraction. However, the use of 14C in studying OC and EC has been limited by technical challenges related to the physical separation of the two fractions and small sample sizes. There is no common procedure for OC/EC 14C analysis, and uncertainty studies have largely focused on the precision of yields. Here, we quantified the uncertainty in 14C measurement of aerosols associated with the isolation and analysis of each carbon fraction with the Swiss_4S thermal-optical analysis (TOA protocol. We used an OC/EC analyzer (Sunset Laboratory Inc., OR, USA coupled to vacuum line to separate the two components. Each fraction was thermally desorbed and converted to carbon dioxide (CO2 in pure oxygen (O2. On average 91% of the evolving CO2 was then cryogenically trapped on the vacuum line, reduced to filamentous graphite, and measured for its 14C content via accelerator mass spectrometry (AMS. To test the accuracy of our set-up, we quantified the total amount of extraneous carbon introduced during the TOA sample processing and graphitization as the sum of modern and fossil (14C-depleted carbon introduced during the analysis of fossil reference materials (adipic acid for OC and coal for EC and contemporary standards (oxalic acid for OC and rice char for EC as a function of sample size. We further tested our methodology by analyzing five ambient airborne particulate matter (PM2.5 samples with a range of OC and EC concentrations and 14C contents in an interlaboratory comparison. The total modern and fossil carbon blanks of our set-up were 0.8 ± 0.4 and 0.67 ± 0.34 μg C

  10. Accuracy and precision of 14C-based source apportionment of organic and elemental carbon in aerosols using the Swiss_4S protocol

    Science.gov (United States)

    Mouteva, G. O.; Fahrni, S. M.; Santos, G. M.; Randerson, J. T.; Zhang, Y.-L.; Szidat, S.; Czimczik, C. I.

    2015-09-01

    Aerosol source apportionment remains a critical challenge for understanding the transport and aging of aerosols, as well as for developing successful air pollution mitigation strategies. The contributions of fossil and non-fossil sources to organic carbon (OC) and elemental carbon (EC) in carbonaceous aerosols can be quantified by measuring the radiocarbon (14C) content of each carbon fraction. However, the use of 14C in studying OC and EC has been limited by technical challenges related to the physical separation of the two fractions and small sample sizes. There is no common procedure for OC/EC 14C analysis, and uncertainty studies have largely focused on the precision of yields. Here, we quantified the uncertainty in 14C measurement of aerosols associated with the isolation and analysis of each carbon fraction with the Swiss_4S thermal-optical analysis (TOA) protocol. We used an OC/EC analyzer (Sunset Laboratory Inc., OR, USA) coupled to a vacuum line to separate the two components. Each fraction was thermally desorbed and converted to carbon dioxide (CO2) in pure oxygen (O2). On average, 91 % of the evolving CO2 was then cryogenically trapped on the vacuum line, reduced to filamentous graphite, and measured for its 14C content via accelerator mass spectrometry (AMS). To test the accuracy of our setup, we quantified the total amount of extraneous carbon introduced during the TOA sample processing and graphitization as the sum of modern and fossil (14C-depleted) carbon introduced during the analysis of fossil reference materials (adipic acid for OC and coal for EC) and contemporary standards (oxalic acid for OC and rice char for EC) as a function of sample size. We further tested our methodology by analyzing five ambient airborne particulate matter (PM2.5) samples with a range of OC and EC concentrations and 14C contents in an interlaboratory comparison. The total modern and fossil carbon blanks of our setup were 0.8 ± 0.4 and 0.67 ± 0.34 μg C, respectively

  11. New {sup 230}Th/U and {sup 14}C ages from Lake Lahontan carbonates, Nevada, USA, and a discussion of the origin of initial thorium

    Energy Technology Data Exchange (ETDEWEB)

    Lin, J.C.; Broecker, W.S.; Anderson, R.F. [Lamont-Doherty Earth Observatory of Columbia Univ., Palisades, NY (United States)] [and others

    1996-08-01

    Five sets of coeval lacustrine carbonate samples from Pleistocene Lake Lahontan in western Nevada were dated by both the AMS {sup 14}C and {sup 230}Th/U isochron methods. All five groups of samples were analyzed for U-Th isotopes by alpha spectrometry and one of the groups was additionally measured by thermal and secondary ionization mass spectrometry (TIMS and SIMS) for comparison. The {sup 14}C ages were corrected to calendar years using the calibration curve recommended by Bard et al. (1992). Without local reservoir correction on the {sup 14}C ages mean {sup 230}Th/U isochron ages of some sets are apparently older than their calendar-corrected {sup 14}C ages by up to 2300 years. Modern carbon contamination of these carbonate samples through recrystallization or deposition of secondary calcite is likely to be responsible for part of the age discrepancies. We explored additional biases associated with the isochron ages, maybe produced by the presence of initial Th coprecipitated from the lake water. It can be shown that if dissolved (hydrogenous) Th is directly incorporated into the pure carbonates, then the three-component mixing among (1) detrital Th, (2) hydrogenous Th adsorbed on detritus, and (3) hydrogenous Th incorporated by the carbonate can introduce a positive age bias. We have developed an approach to estimate the magnitude of this bias of the Lake Lahontan carbonates. The preliminary estimates suggest a positive age bias of 1000 to 2000 years for two sets of the samples. 49 refs., 10 figs., 9 tabs.

  12. Occurrence and concentrations of selected trace elements and halogenated organic compounds in stream sediments and potential sources of polychlorinated biphenyls, Leon Creek, San Antonio, Texas, 2012–14

    Science.gov (United States)

    Wilson, Jennifer T.

    2016-06-23

    The Texas Department of State Health Services issued fish consumption advisories in 2003 and 2010 for Leon Creek in San Antonio, Texas, based on elevated concentrations of polychlorinated biphenyls (PCBs) in fish tissues. The U.S. Geological Survey (USGS) measured elevated PCB concentrations in stream-sediment samples collected during 2007–9 from Leon Creek at Lackland Air Force Base (now known as Joint Base San Antonio-Lackland; the sampling site at this base is hereinafter referred to as the “Joint Base site”) and sites on Leon Creek downstream from the base. This report describes the occurrence and concentrations of selected trace elements and halogenated organic compounds (pesticides, flame retardants, and PCBs) and potential sources of PCBs in stream-sediment samples collected from four sites on Leon Creek during 2012–14. In downstream order, sediment samples were collected from Leon Creek at northwest Interstate Highway 410 (Loop 410), Rodriguez Park, Morey Road, and Joint Base. The USGS periodically collected streambed-sediment samples during low flow and suspended-sediment samples during high flow.

  13. Chromatographic behavior of small organic compounds in low-temperature high-performance liquid chromatography using liquid carbon dioxide as the mobile phase.

    Science.gov (United States)

    Motono, Tomohiro; Nagai, Takashi; Kitagawa, Shinya; Ohtani, Hajime

    2015-07-01

    Low-temperature high-performance liquid chromatography, in which a loop injector, column, and detection cell were refrigerated at -35ºC, using liquid carbon dioxide as the mobile phase was developed. Small organic compounds (polyaromatic hydrocarbons, alkylbenzenes, and quinones) were separated by low-temperature high-performance liquid chromatography at temperatures from -35 to -5ºC. The combination of liquid carbon dioxide mobile phase with an octadecyl-silica (C18 ) column provided reversed phase mode separation, and a bare silica-gel column resulted in normal phase mode separation. In both the cases, nonlinear behavior at approximately -15ºC was found in the relationship between the temperature and the retention factors of the analytes (van't Hoff plots). In contrast to general trends in high-performance liquid chromatography, the decrease in temperature enhanced the separation efficiency of both the columns.

  14. Compound-specific carbon isotopes from Earth's largest flood basalt eruptions directly linked to the end-Triassic mass extinction.

    Science.gov (United States)

    Whiteside, Jessica H; Olsen, Paul E; Eglinton, Timothy; Brookfield, Michael E; Sambrotto, Raymond N

    2010-04-13

    A leading hypothesis explaining Phanerozoic mass extinctions and associated carbon isotopic anomalies is the emission of greenhouse, other gases, and aerosols caused by eruptions of continental flood basalt provinces. However, the necessary serial relationship between these eruptions, isotopic excursions, and extinctions has never been tested in geological sections preserving all three records. The end-Triassic extinction (ETE) at 201.4 Ma is among the largest of these extinctions and is tied to a large negative carbon isotope excursion, reflecting perturbations of the carbon cycle including a transient increase in CO(2). The cause of the ETE has been inferred to be the eruption of the giant Central Atlantic magmatic province (CAMP). Here, we show that carbon isotopes of leaf wax derived lipids (n-alkanes), wood, and total organic carbon from two orbitally paced lacustrine sections interbedded with the CAMP in eastern North America show similar excursions to those seen in the mostly marine St. Audrie's Bay section in England. Based on these results, the ETE began synchronously in marine and terrestrial environments slightly before the oldest basalts in eastern North America but simultaneous with the eruption of the oldest flows in Morocco, a CO(2) super greenhouse, and marine biocalcification crisis. Because the temporal relationship between CAMP eruptions, mass extinction, and the carbon isotopic excursions are shown in the same place, this is the strongest case for a volcanic cause of a mass extinction to date.

  15. Effects of time passage and distance on distribution of carbon-14 among parts of rice during growth period at Korean CANDU plant

    International Nuclear Information System (INIS)

    The pattern of carbon-14 (C-14) distribution among parts of rice growing in the vicinity of the Korean CANDU plant during the growth period was investigated. Six-time samplings of rice and air were performed in seven fields from rice planting to harvest, and the measurements of C-14 content were made by using liquid scintillation counter on the air and each of available parts of the rice such as root, stem, crust and ear. The results illustrated that C-14 showed a relatively even distribution among parts of rice during the growth period implying C-14 accumulation was more dependent on interactions among the parts such as transportation of nutrients than on photosynthesis occurring only in stem that has chlorophyll. Also it was observed that the difference of C-14 concentration between each part of rice and the air decreased with time indicating that the time was needed for C-14 to reach equilibrium between both sides. The radius within which C-14 released from the Wolsong plant could have a significant effect on the C-14 concentrations of the parts was observed to be about 5 km. (author)

  16. The evolution of a tropical rainforest/grassland mosaic in southeastern Brazil since 28,000 14C yr BP based on carbon isotopes and pollen records

    Science.gov (United States)

    Ruiz Pessenda, Luiz Carlos; De Oliveira, Paulo Eduardo; Mofatto, Milene; de Medeiros, Vanda Brito; Francischetti Garcia, Ricardo José; Aravena, Ramon; Bendassoli, José Albertino; Zuniga Leite, Acácio; Saad, Antonio Roberto; Lincoln Etchebehere, Mario

    2009-05-01

    The lack of paleoecological records from the montane Atlantic Rainforest of coastal Brazil, a hotspot of biological diversity, has been a major obstacle to our understanding of the vegetational changes since the last glacial cycle. We present carbon isotope and pollen records to assess the impact of the glaciation on the native vegetation of the Serra do Mar rainforest in São Paulo, Brazil. From ca. 28,000 to ˜ 22,000 14C yr BP, a subtropical forest with conifer trees is indicative of cool and humid conditions. In agreement carbon isotopic data on soil organic matter suggest the presence of C 3 plants and perhaps C 4 plants from ˜ 28,000 to ˜ 19,000 14C yr BP. The significant increase in the sedimentation rate and algal spores from ˜ 19,450 to ˜ 19,000 14C yr BP indicates increasing humidity, associated to an erosion process between ˜ 19,000 and ˜ 15,600 14C yr BP. From ˜ 15,600 14C yr BP to present there is a substantial increase in arboreal elements and herbs, indicating more humid and warmer climate. From ˜ 19,000 to ˜ 1000 14C yr BP, δ 13C values indicated the predominance of C 3 plants. These results are in agreement with studies in speleothems of caves, which suggest humid conditions during the last glacial maximum.

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

    Energy Technology Data Exchange (ETDEWEB)

    Subramanian, Vaidyanathan; Murugesan, Sankaran

    2014-04-29

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

  18. Experimental urolithiasis : Part V - Role of dietary carbonate in the etiology of the disease using radioactive 14C-potassium bicarbonate

    International Nuclear Information System (INIS)

    Incorporation of 14C-potassium bicarbonate in rat kidney, bladder, blood and bladder contents was assessed to study the role of dietary carbonate in urolithiasis. Male rats (23) were fed carbonate-free diet and water, 19 of which were surgically induced for bladder stones and the remaining sham-operated. Total elimination of carbonate both from diet and drinking water lowered the incidence of stone by 63% as compared with a parallel group fed normal diet and tap water. At sacrifice, 5 μCi of 14C-KHCO3 were injected (ip) into each animal. Higher counts in the serum and kidney, than that in the contents of the bladder were noted on both types of diet. Feeding of normal diet and tap water, led to a significant increase (P14C uptake, and their relative distribution (as indicated by the total counts incorporated) in the various tissues of stoneformers and non-stoneformers as compared to controls, reflects individual differences in the handling of carbonate by each tissue. (auth.)

  19. Test of the suitability of ECOPATH/ECOSIM modelling software as a compliment to estimate flows of carbon, C-14 and radionuclides in the Oeregrundsgrepen area

    Energy Technology Data Exchange (ETDEWEB)

    Sandberg, Johannes [Stockholm Univ. (Sweden). Dept. of Systems Ecology

    2004-04-01

    In this study it was evaluated whether the ECOPATH with ECOSIM software could be used as a standard platform to facilitate for radioecologists to construct and study transport and accumulation of radionuclides in aquatic food webs. The evaluation was based upon: 1) a previously published food web model of carbon/carbon-14 flow for the Oeregrundsgrepen area, Baltic Sea, 2) a generic model, 3) an ECOSIM model and 4) an ECOTRACE model. The results presented clearly shows that there is great potential for a successful development of this scientific approach in the future. The original carbon flows and assumptions was easily incorporated into the ECOPATH with ECOSIM modelling environment. The carbon flows differed only negligible between the two models, except for the benthic flows, which was more accurately described in this study. Further, by using ECOPATH it was easily discovered that the growth efficiencies used in the original model was quite high, being 47% for most of the heterotrophs, which are high from an ecological point of view. However, that is probably due to differences in how the carbon flows have been estimated in the original versus the present study. It is likely, however that the carbon demand has been underestimated in the original model. The generic model was parameterised from data available through the software as well from the diets and assumptions used in the original carbon model. The use of these parameters resulted in carbon flows, which was between 0.7 to 11 times the flows estimated by the ECOPATH model. The difference was greatest for primary producers being 3.7 to 11 times the original flows. Thus, depending on the question one is addressing it was suggested that the use of generic parameters is best for making test models of carbon and radionuclide flows in ecosystems, where the data set for validation is limited. Finally, the ECOPATH and ECOSIM model was well suited to drive a C-14 flow model, such as ECOTRACER for each of the

  20. Test of the suitability of ECOPATH/ECOSIM modelling software as a compliment to estimate flows of carbon, C-14 and radionuclides in the Oeregrundsgrepen area

    International Nuclear Information System (INIS)

    In this study it was evaluated whether the ECOPATH with ECOSIM software could be used as a standard platform to facilitate for radioecologists to construct and study transport and accumulation of radionuclides in aquatic food webs. The evaluation was based upon: 1) a previously published food web model of carbon/carbon-14 flow for the Oeregrundsgrepen area, Baltic Sea, 2) a generic model, 3) an ECOSIM model and 4) an ECOTRACE model. The results presented clearly shows that there is great potential for a successful development of this scientific approach in the future. The original carbon flows and assumptions was easily incorporated into the ECOPATH with ECOSIM modelling environment. The carbon flows differed only negligible between the two models, except for the benthic flows, which was more accurately described in this study. Further, by using ECOPATH it was easily discovered that the growth efficiencies used in the original model was quite high, being 47% for most of the heterotrophs, which are high from an ecological point of view. However, that is probably due to differences in how the carbon flows have been estimated in the original versus the present study. It is likely, however that the carbon demand has been underestimated in the original model. The generic model was parameterised from data available through the software as well from the diets and assumptions used in the original carbon model. The use of these parameters resulted in carbon flows, which was between 0.7 to 11 times the flows estimated by the ECOPATH model. The difference was greatest for primary producers being 3.7 to 11 times the original flows. Thus, depending on the question one is addressing it was suggested that the use of generic parameters is best for making test models of carbon and radionuclide flows in ecosystems, where the data set for validation is limited. Finally, the ECOPATH and ECOSIM model was well suited to drive a C-14 flow model, such as ECOTRACER for each of the

  1. Magnesium compounds

    Science.gov (United States)

    Kramer, D.A.

    2006-01-01

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

  2. Compound odontoma

    Directory of Open Access Journals (Sweden)

    Monica Yadav

    2012-01-01

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

  3. {sup 14}C chronology of the oldest Scandinavian church in use. An AMS/PIXE study of lime lump carbonate in the mortar

    Energy Technology Data Exchange (ETDEWEB)

    Lindroos, Alf, E-mail: alf.lindroos@abo.fi [Geology and Mineralogy, Department of Natural Sciences, Åbo Akademi University (Finland); Art History, Faculty of Art, Åbo Akademi University (Finland); Ranta, Heikki [Diocese of Lund, Church of Sweden (Sweden); Heinemeier, Jan [AMS " 1" 4C Dating Laboratory, Department of Physics and Astronomy, University of Aarhus (Denmark); Lill, Jan-Olof [Accelerator Laboratory, Turku PET Centre, Åbo Akademi University (Finland)

    2014-07-15

    Mortar dating was applied to newly revealed, original mortar in the church of Dalby in Scania, southern Sweden which is considered to be the oldest still standing church in Scandinavia. Small white lime lumps were sampled by chipping from the supporting pillars in the interior of the church. Special emphasis was in sampling lime lumps because the church is situated in the Scania limestone area and aggregate limestone contamination was anticipated in the bulk mortars. Earlier studies have, however, shown that lime lumps do not contain aggregate material but only possible limestone rests from incomplete calcination. The sampled material was prepared for radiocarbon AMS dating. The carbonate in the lime lumps was hydrolyzed according to the sequential leaching technique developed for the Århus {sup 14}C laboratory in Denmark. Prior to the hydrolysis the lime lumps were examined for dead-carbon contamination using a stereo microscope and cathodoluminescence. The lime lumps displayed heterogeneous carbonate luminescence. This is, however, common and it was not considered a problem because carbonate growth in changing pH/Eh conditions often leads to changing luminescence colors. Two lumps had little dead carbon contamination and an early second millennium {sup 14}C signature. One lump, however, seemed to be heavily contaminated with dead carbon. Since the sample passed the microscopic screening, the leftovers of the lump was subjected to PIXE analysis and compared with the other two lumps. The well-defined, early 2nd millennium {sup 14}C age of the lime lumps of this particular church is an important contribution to the discussion on stone church chronology in Scandinavia.

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

    International Nuclear Information System (INIS)

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

  5. Labeled plasma metabolites of L-methyl-hydrogen-3-methionine and L-methyl-carbon-14-methionine in the dog

    International Nuclear Information System (INIS)

    The validity of the mathematical models that attempt to describe positron emission tomography (PET) images produced with [11CH3] methionine in terms of rates of local cerebral protein synthesis has yet to be established. A major objection to current models is that the use of methionine labeled at the methyl position results in the dispersal of the label among various methyl-accepting compounds that appear in the plasma and may then enter the brain. One approach to overcoming this problem has been the use of ''standard'' corrections for the activity contributed to plasma by labeled plasma protein and labeled serine. In order to determine the validity of this approach, the metabolic fate of labeled methionine was studied in six dogs. After injection with either [C3H3] methionine or [14CH3] methionine arterial blood was sampled. Plasma fractions containing protein were separated by fast gel filtration, counted with standard scintillation techniques, and their radioactivity was compared with total plasma radioactivity. Plasma was also separated by high-pressure liquid chromatography into methionine, serine, and nonmethionine or serine-containing fractions. These fractions were counted, and their radioactivity was compared with total plasma radioactivity. Labeled protein appeared in plasma about 20 minutes postinjection and then increased steadily. Labeled serine also appeared and reached a peak value of 9.4 +/- 2.1% of plasma activity at 40 minutes. Of greatest interest was the appearance in later plasma samples of increasing amounts of activity contained in nonserine low molecular weight metabolites of methionine. At 40 minutes, those metabolites made up 27 +/- 6.9% of total plasma activity

  6. Δ14C and δ13C as tracers of organic carbon in Baltic Sea sediments collected in coastal waters off Lithuania and in the Gotland Deep

    International Nuclear Information System (INIS)

    Signatures of Δ14C and δ13C of total organic carbon in sediments as well as of total lipid extracts and phospholipid-derived fatty acid fractions isolated from the surface (0-3 cm) sediments collected in the Curonian Lagoon and in the open Baltic Sea were studied. An endmember mixing-model approach was applied to estimate relative contributions of the marine and terrestrial inputs to organic carbon in sediments, and to elucidate a possible leakage of chemical warfare agents at the Gotland Deep dumpsite. (author)

  7. HYDROGENATION OF POLYCYCLIC AROMATIC COMPOUNDS USING NI SUPPORT ON H-BETA ZEOLITE IN SUPERCRITICAL CARBON DIOXIDE

    Science.gov (United States)

    The primary rationale for use of supercritical carbon dioxide as a solvent in hydrogenation is the elimination of mass transfer limitations, through enhancement of the solubility of hydrogen at the reaction locus. Hydrogenation of anthracene was performed using NiHB-zeolite catal...

  8. Syntheses and properties of a family of new compounds RE3Sb3Co2O14 (RE=La, Pr, Nd, Sm–Ho) with an ordered pyrochlore structure

    International Nuclear Information System (INIS)

    Isostructural compounds RE3Sb3Co2O14 (RE=La, Pr, Nd, Sm–Ho) with an ordered pyrochlore structure were synthesized. The structure of La3Sb3Co2O14 was solved ab initio based on powder XRD data, and refined by combining with high resolution neutron diffraction data. La3Sb3Co2O14 crystallizes in the space group R-3m with the unit cell parameters a=7.52954(2) Å and c=17.59983(6) Å. The structures of other members in this family are confirmed by Rietveld refinement using powder X-ray diffraction data. The cations (RE, Sb and Co) in RE3Sb3Co2O14 are orderly distributed, presenting as [RE3Co][Sb3Co]O14 formula, and giving rise to two distinctive Kagome lattices constructed by RE3+ and Sb5+, respectively. Co2+ occupies 8-coordinated and 6-coordinated environments, showing low spin (S=1/2) and high spin (S=3/2) states respectively. The magnetic susceptibility and UV–visual spectroscopy supports the magnetic observation. TDDFT calculation was performed to interpret the electronic states. The compounds [RE3Co][Sb3Co]O14 provide a profound example in which the ideal 2D Kagome lattice is derived from the 3D pyrochlore-type structure by an ordered distribution of the metal cations. - Graphical abstract: La3Sb3Co2O14 crystallizes in a pyrochlore related structure with an ordered distribution of cations, giving rise to two sets of ideal 2D Kagome lattices formed by La3+ or Sb5+ respectively. This rhombohedral pyrochlore is a tolerant structure for stable compounds composed by many light rare-earth and d-transition elements. Substituting Zn2+ or Mg2+ for Co2+ will provide a series of compounds useful for studying magnetic interactions in the rare-earth Kagome lattices. - Highlights: • Pyrochlore-type La3Sb3Co2O14 shows an ordered distribution of cations in its structure. • It presents two sets of ideal 2D Kagome lattices formed by La3+ or Sb5+, respectively. • A family of isostructural compounds RE3Sb3Co2O14 (RE=Pr, Nd, Sm–Ho) were realized. • Co2+ presents two spin

  9. Amperometric detection in the presence of carbon nanotubes dispersed in background electrolyte: Evaluating its suitability for capillary electrokinetic chromatography separations of polyphenolic compounds.

    Science.gov (United States)

    Moreno, Mónica; Sánchez Arribas, Alberto; Bermejo, Esperanza; Zapardiel, Antonio; Chicharro, Manuel

    2015-08-01

    This work reports on the positive effects observed upon both the separation and analytical signals in electrophoretic separations of selected phenolic compounds when using aqueous BGE containing carbon nanotubes (CNTs) in connection to electrochemical detection (ECD). The influence of the presence of surfactant-coated CNTs in the BGE upon the amperometric response of probe compounds was evaluated under hydrodynamic regime in capillary flow injection experiments as well as electrophoretic separations. Among the surfactants employed to disperse CNTs within BGE, SDS shows the best results in terms of dispersion stability and degree of dispersion of the CNTs. ECD allows working with BGEs containing CNTs concentrations of, at least, 24.0 mg/L without increasing of baseline noise, on the opposite to that reported when using UV-visible detection, and the presence of CNTs in the BGE improves the electrochemical response of some of the tested compounds. These benefits were reflected in higher sensibility in the electrochemical signal and additional improved resolution in the electrophoretic separation of (±)-catechin and sinapic acid when using these BGE containing CNTs.

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

    Science.gov (United States)

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

    2015-08-01

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

  11. Nature and Origin of Variations in Late-Glacial and Holocene Atmospheric CARBON-14 as Revealed by Global Carbon Cycle Modeling

    Science.gov (United States)

    Braziunas, Thomas Frank

    1990-01-01

    Simulations with a global box-diffusion ^{14}C model indicate that the millennium- and century-scale atmospheric Delta ^{14}C variations during the Holocene are more likely explained by fluctuations in ^ {14}C production rate (Q) than by changes in air-sea CO_2 exchange rate (F) or internal ocean mixing (parameterized as an "eddy diffusivity" K_{rm z}. The ^{14}C reservoir model deconvolves histories for each of these three processes that are compatible with a 96-yr bi-decadal atmospheric (tree-ring)Delta^{14}C record assuming alternative pre-Holocene ^ {14}C conditions. Holocene microparticle concentrations in ice cores and dust grain sizes in marine sediment cores disagree with the model-derived global wind speeds necessary to explain (through F variations) the millennium-scale trends in atmospheric Delta ^{14}C. Alternately, foram ^{14}C data do not support the history in the oceanic ventilation index generated by millennium -scale K_{rm z} variations. Coral ^{14}C data for recent centuries conflict with the marine Delta ^{14}C history associated with century-scale variations in F or K_{ rm z} but are consistent with changes in ^{14}C production rate. The ^{14}C production rates derived theoretically from an 11,000-yr record of averaged global dipole moments strongly correlate with the Q history required to explain tree-ring Delta ^{14}C. Several pre-Holocene Q histories were calculated from limited dipole moment data available for the past 30,000 yrs and do not contradict ^{234}U/^ {230}Th-calibrated coral ^ {14}C measurements. Relative variations in Greenland ice-core ^{10}Be concentrations (reflecting changes in ^ {10}Be production) over the past 9000 yrs also correlate strongly with tree-ring Q fluctuations except for a 4500-3500 BC discrepancy. Simulations of transient variations in Q, F, and K_{rm z} supplement previous studies of alternative steady-state ^ {14}C situations. The modeling of combined climate and production rate scenarios (i.e. F + K _{rm z

  12. Jean-François Gallotte, Joëlle Malberg, Carbone 14 le film, Les Mutins de Pangée

    OpenAIRE

    Curien, Julie

    2014-01-01

    Carbone 14 le film est un témoignage sur le mouvement des radios libres, à travers l'exemple de « Carbone 14 », « la radio active » devenue « la radio qui vous encule par les oreilles ». Filmé en 4 jours à la rentrée 1982, avec du matériel volé, le film ovni de Jean-François Galotte et Joëlle Malberg est sélectionné au Festival de Cannes en 1983. Il fait un tollé qui retombe comme une crêpe, aux oubliettes : on n'en parle plus avant... 2011, trente ans après la création de la radio culte et c...

  13. Le carbone 14 : progrès récents et limitations de la méthode de datation

    OpenAIRE

    J. C. Duplessy; Arnold, M; Bard, E.; Cortijo, E.; Labeyrie, L.; Laj, C.; Lehman, B; Mazaud, A.; M. Paterne; Tisnerat, N.; L. Vidal

    1998-01-01

    La méthode de datation par le carbone 14 a permis l'établissement d'une échelle chronologique du Quaternaire Supérieur et a contribué à la découverte de phénomènes insoupçonnés comme l'existence de variations climatiques abruptes et de grande amplitude pendant la dernière période glaciaire et la déglaciation qui l'a terminée. L'effort continu pour comparer les âges carbone 14 avec les âges calendaires a été maintenant étendu au delà de 30 000 ans, même si le nombre de mesures est encore trop ...

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

    Institute of Scientific and Technical Information of China (English)

    2007-01-01

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

  15. AMS-{sup 14}C measurements for the carbonate platform of the offshore Campos Basin, Rio de Janeiro State, Brazil

    Energy Technology Data Exchange (ETDEWEB)

    Coimbra, Melayne M. E-mail: melayne@onda.com.br; Barbosa, Catia F.; Soares-Gomes, Abilio; Silva, Cleverson G.; Rios-Netto, Aristoteles; Mueller, Ken A

    2000-10-01

    As part of our accelerator mass spectrometry (AMS) program in Brazil we prepared and measured some red algae carbonate crust samples from Campos Basin, Rio de Janeiro, Brazil. The measurements were performed at Purdue Rare Isotope Measurement Laboratory (PRIME Lab), Purdue University, IN, USA. This carbonate material is interlaminated with foraminiferal lime mud reflecting recurrent intervals of carbonate development, which might be linked to outer-shelf oceanographic circulation.

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

    International Nuclear Information System (INIS)

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

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

    Energy Technology Data Exchange (ETDEWEB)

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

    2015-09-05

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

  18. Synthesis of carbon-14 labelled (5Z)-4-bromo-5-(bromomethylene)-2(5H)-furanone:

    DEFF Research Database (Denmark)

    Persson, T.; Johansen, S.K.; Martiny, L.;

    2004-01-01

    The potent quorum sensing inhibitor (5Z)-4-bromo-5-(bromomethylene)-2(5H)-[2-C-14]furanone has been prepared in five steps in 7.7% overall yield starting from bromo[1-C-14]acetic acid. Condensation of ethyl bromo[1-C-14]acetate with ethyl acetoacetate followed by decarboxylation was accelerated...

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

    Science.gov (United States)

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

    2013-12-01

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

  20. Exposure to perfluorononanoic acid combined with a low-dose mixture of 14 human-relevant compounds disturbs energy/lipid homeostasis in rats

    DEFF Research Database (Denmark)

    Skov, Kasper; Kongsbak, Kristine Grønning; Hadrup, Niels;

    2015-01-01

    Humans are constantly exposed to a significant number of compounds and many are readily detected in human body fluids. Worryingly, several of these compounds are either suspected to be, or have already been shown to be harmful to humans either individually or in combination. However, the potentia...

  1. Hydrothermal Synthesis and Characterization of a Novel Organic Inorganic Hybrid Compound [Co(dien)2](dienH3)(H3O)7[P2Mo5O23]2·14H2O

    Institute of Scientific and Technical Information of China (English)

    ZHAO Weifeng; ZHANG Lianmeng; JIN Surong

    2007-01-01

    A new compound,[Co(dien)2](dienH3)(H3O)7[P2Mo5O23]2·14H2O, has been hydrothermallly synthesized by using Na2MoO4,CoC12, H3PO4 and dien, and structurally characterized by elemental analysis,X-ray powder diffraction analysis, SEM, IR and TG analysis. The results show that the compound is composed of a polyanion [P2Mo5O23]212- , complex [Co(dien)2]2+ cation, protonated [dienH3]3+ , and forteen crystallization water molecule.

  2. On 14C-based methods for measuring the biogenic carbon fraction in fuels and flue gases

    NARCIS (Netherlands)

    Palstra, Sanne Waltje Lieze

    2016-01-01

    Several international regulations distinguish between carbon from biomass and carbon from fossil raw materials for different materials and CO2 emissions. Due to these regulations it can be financially beneficial for companies to claim for instance their products to originate from 100% biomass, that

  3. Carbon cycling in primary production bottle incubations: inferences from grazing experiments and photosynthetic studies using 14C and 18O in the Arabian Sea

    Science.gov (United States)

    Laws, Edward A.; Landry, Michael R.; Barber, Richard T.; Campbell, Lisa; Dickson, Mary-Lynn; Marra, John

    Estimates of photosynthesis based on the incorporation of 14C-labeled inorganic carbon into particulate carbon were compared to estimates of gross photosynthesis based on net O 2 production and the production of 18O2 from H218O during the US Joint Global Ocean Flux Study (US JGOFS) Arabian Sea process cruises. For samples incubated below the surface and at optical depthsMehler reaction, photorespiration, dark respiration, excretion, and grazing effects on the two estimates of photosynthesis. The 14C uptake : gross photosynthesis ratio was distinctly higher (0.62) for samples incubated at the surface. This result is likely due to UV light effects, since the O 2 and 14C incubations were done in quartz and polysulfone bottles, respectively. The 14C uptake : gross photosynthesis ratio was lower (0.31) for bottles incubated at optical depths>3. This result probably reflects an increase in the ratio of dark respiration to net photosynthesis in the vicinity of the compensation light level.

  4. Thiophenic Sulfur Compounds Released During Coal Pyrolysis.

    Science.gov (United States)

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

    2013-06-01

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

  5. Biomarker and carbon isotope constraints (δ{sup 13}C, Δ{sup 14}C) on sources and cycling of particulate organic matter discharged by large Siberian rivers draining permafrost areas

    Energy Technology Data Exchange (ETDEWEB)

    Winterfeld, Maria

    2014-08-15

    detectable in changing lignin biomarker composition, diagenetic alteration, and radiocarbon age. The second part of this thesis investigates past permafrost dynamics and the possible permafrost/wetland climate feedback during the last deglaciation and Early Holocene. The Amur hinterland in East Siberia was most likely characterized by extensive permafrost during the last glacial maximum and is today permafrost-free with the exception of small areas in the northern reaches of the catchment. The organic matter flux of the Amur River into its receiving basin, the Okhotsk Sea, was reconstructed for the last 16,000 years in a high-resolution AMS {sup 14}C-dated sediment core from the Sakhalin continental margin, based on organic geochemical multi-proxy data and compound-specific radiocarbon dating of n-alkanoic acids. Within the deglacial discharge maximum of organic matter to the Okhotsk Sea, two peaks of organic matter release episodes; the first occurring during the Bolling-Allerod warm phase, and the second, larger one after Termination Ib in the earliest Preboreal could be identified. The results highlight the sensitivity of the Amur drainage basin carbon reservoir to rapid deglacial temperature and precipitation changes. It is hypothesized that large amounts of carbon were activated upon deglacial permafrost thawing within this southernmost Siberian large catchment and quickly transferred to the oceanic carbon reservoir via riverine freshwater transport into the Okhotsk Sea and the North Pacific.

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

    International Nuclear Information System (INIS)

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

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

    Science.gov (United States)

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

    2016-01-01

    Molecular distributions and stable carbon isotopic compositions (δ(13)C) of n-alkanes, fatty acids and n-alcohols were investigated in urban aerosols from Beijing, northern China to better understand the sources and long-range atmospheric transport of terrestrial organic matter during polluted and clear days in winter. n-Alkanes (C19-C36), fatty acids (C8-C32) and n-alcohols (C16-C32) detected in Beijing aerosols are characterized by the predominance of C23, C16 and C28, respectively. Carbon preference index (CPI) values of n-alkanes, the ratios of the sum of odd-numbered n-alkanes to the sum of even-numbered n-alkanes, are close to 1, indicating a heavy influence of fossil fuel combustion. Relatively higher ratios of C(18:0+16:0)/C(18:n+16:1) (fatty acids) on clear days than polluted days indicate that long-distance transport and/or photochemical aging are more significant during clear days. δ(13)C values of n-alkanes and low molecular weight fatty acids (C16:0, C18:0) ranged from -34.1 to -24.7% and -26.9 to -24.6%, respectively, which are generally heavier on polluted days than those on clear days. Such a wide range suggests that atmospheric lipids in Beijing aerosols originate from multiple sources and encounter complicated atmospheric processes during long-range transport in North China. PMID:27270951

  8. Bio-Carbon Accounting for Bio-Oil Co-Processing: 14C and 13C/12C

    Energy Technology Data Exchange (ETDEWEB)

    Mora, Claudia I. [Los Alamos National Lab. (LANL), Los Alamos, NM (United States); Li, Zhenghua [Los Alamos National Lab. (LANL), Los Alamos, NM (United States); Vance, Zachary [Los Alamos National Lab. (LANL), Los Alamos, NM (United States)

    2016-06-21

    This is a powerpoint presentation on bio-carbon accounting for bio-oil co-processing. Because of the overlapping range in the stable C isotope compositions of fossil oils and biooils from C3-type feedstocks, it is widely thought that stable isotopes are not useful to track renewable carbon during co-production. In contrast, our study demonstrates the utility of stable isotopes to: • capture a record of renewable carbon allocation between FCC products of co-processing • record changes in carbon apportionments due to changes in reactor or feed temperature Stable isotope trends as a function of percent bio-oil in the feed are more pronounced when the δ13C of the bio-oil endmember differs greatly from the VGO (i.e., it has a C4 biomass source–corn stover, switch grass, Miscanthus, sugarcane– versus a C3 biomass source– pine, wheat, rice, potato), but trends on the latter case are significant for endmember differences of just a few permil. The correlation between measured 14C and δ13C may be useful as an alternative to carbon accounting, but the relationship must first be established for different bio-oil sources.

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

    Science.gov (United States)

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

    2014-06-01

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

  10. Stable sulfur and carbon isotope investigations of pore-water and solid-phase compounds in sediments of the Chapopote Asphalt Volcano, southern Gulf of Mexico

    Science.gov (United States)

    Wilhelm, T.; Bruechert, V.; Pape, T.; Schubotz, F.; Kasten, S.

    2007-05-01

    During R/V Meteor cruise M67 2a/b (March-April 2006) to the Asphalt Volcanoes of the southern Gulf of Mexico two gravity cores were retrieved from the central depression of the Chapopote Knoll which contained viscous oil/asphalt a few meters below the sediment surface. Also several push cores were taken with the remotely operated vehicle (ROV) QUEST at sites where oil/asphalt reached closely below the sediment surface. From these cores solid-phase and pore-water samples were taken for on-board and subsequent shore-based analyses. Together with a core taken from a background site which is not influenced by asphalt/oil seepage these sediment and pore water samples are currently subject to detailed analyses of (1) the stable sulfur isotopic composition of both dissolved (sulfate and sulfide) and solid-phase (iron monosulfides, pyrite) sulfur compounds, and (2) the composition and stable carbon isotopic signatures of hydrocarbon gases. The major aims of these investigations are to identify whether and to which extent the upward migration of oil, asphalt and gas (1) stimulates biogeochemical processes and turn-over rates, and (2) influences the stable sulfur isotopic signatures of both dissolved and solid phase sulfur compounds. Furthermore, we seek to determine the potential of these - possibly unusual - stable sulfur isotopic signals of solid-phase sulfides to reconstruct hydrocarbon seepage in older geological records and to elucidate how the composition and the stable carbon isotopic signatures of the hydrocarbon gases are altered by the action of typical chemosynthetic communities thriving at these sites.

  11. Synthesizing the Use of Carbon Isotope (14C and 13C) Approaches to Understand Rates and Pathways for Permafrost C Mobilization and Mineralization

    Science.gov (United States)

    Estop-Aragones, C.; Olefeldt, D.; Schuur, E.

    2015-12-01

    To better understand the permafrost carbon (C) feedback it is important to synthesize our current knowledge, and knowledge gaps, of how permafrost thaw can cause in situ mineralization or downstream mobilization of aged soil organic carbon (SOC) and the rate of this release. This potential loss of old SOC may occur via gaseous flux of CO2 and CH4 exchanged between soil and the atmosphere and via waterborne flux as DOC, POC (and their subsequent decomposition and release to the atmosphere). Carbon isotope (14C and 13C) approaches have been used to estimate both rates and pathways for permafrost C mobilization and mineralization. Radiocarbon (14C) has been used to estimate the contribution of aged C to overall respiration or waterborne C export. We aim to contrast results from radiocarbon studies, in order to assess differences between ecosystems (contrasting wet and dry ecosystems), thaw histories (active layer deepening or thermokarst landforms), greenhouse gas considered (CO2 and CH4) and seasons. We propose to also contrast methodologies used for assessing the contribution of aged C to overall C balance, and include studies using 13C data. Biological fractionation of 13C during both uptake and decomposition has been taken advantage of both in order to aid the interpretation of 14C data and on its own to assess sources and mineralization pathways. For example, 13C data has been used to differentiate between CH4 production pathways, and the relative contribution of anaerobic CO2 production to overall respiration. Overall, carbon isotope research is proving highly valuable for our understanding of permafrost C dynamics following thaw, and there is a current need to synthesize the available literature.

  12. Synthesis and purification of carbon-14 labelled 1, 1-hexamethylene-bis [5-(4-chlorophenyl)biguanide] (chlorhexidine, 'Hibitane')

    International Nuclear Information System (INIS)

    Two syntheses of [14C] chlorhexidine ('Hibitane') with the label specifically incorporated in two separate molecular positions are described. Ring labelled chlorhexidine prepared from p-chloro[U-14C]aniline was obtained with a molar specific activity of 27.9 mCi/mmol. Chain labelled material, where the 14C label was incorporated in the 1 and 6 positions of the hexamethylene bridge, was prepared from [1, 6 14C]-adiponitrile, with a molar specific activity of 11.5 mCi/mmol. Several methods of purification are described. (author)

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

    Science.gov (United States)

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

    2016-02-14

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

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

    Science.gov (United States)

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

    2009-11-01

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

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

    Directory of Open Access Journals (Sweden)

    F. Bettin

    2014-06-01

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

  16. High extraction efficiency for polar aromatic compounds in natural water samples using multiwalled carbon nanotubes/Nafion solid-phase microextraction coating.

    Science.gov (United States)

    Chen, Wenfeng; Zeng, Jingbin; Chen, Jinmei; Huang, Xiaoli; Jiang, Yaqi; Wang, Yiru; Chen, Xi

    2009-12-25

    A novel solid-phase microextraction (SPME) fiber coated with multiwalled carbon nanotubes (MWCNTs)/Nafion was developed and applied for the extraction of polar aromatic compounds (PACs) in natural water samples. The characteristics and the application of this fiber were investigated. Electron microscope photographs indicated that the MWCNTs/Nafion coating with average thickness of 12.5microm was homogeneous and porous. The MWCNTs/Nafion coated fiber exhibited higher extraction efficiency towards polar aromatic compounds compared to an 85microm commercial PA fiber. SPME experimental conditions, such as fiber coating, extraction time, stirring rate, desorption temperature and desorption time, were optimized in order to improve the extraction efficiency. The calibration curves were linear from 0.01 to 10microgmL(-1) for five PACs studied except p-nitroaniline (from 0.005 to 10microgmL(-1)) and m-cresol (from 0.001 to 10microgmL(-1)), and detection limits were within the range of 0.03-0.57ngmL(-1). Single fiber and fiber-to-fiber reproducibility were less than 7.5 (n=7) and 10.0% (n=5), respectively. The recovery of the PACs spiked in natural water samples at 1microgmL(-1) ranged from 83.3 to 106.0%.

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

    Science.gov (United States)

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

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

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

    Energy Technology Data Exchange (ETDEWEB)

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

    2009-02-01

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

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

    Science.gov (United States)

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

    2016-06-01

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

  20. Polar organic compounds in pore waters of the Chesapeake Bay impact structure, Eyreville core hole: Character of the dissolved organic carbon and comparison with drilling fluids

    Science.gov (United States)

    Rostad, C.E.; Sanford, W.E.

    2009-01-01

    Pore waters from the Chesapeake Bay impact structure cores recovered at Eyreville Farm, Northampton County, Virginia, were analyzed to characterize the dissolved organic carbon. After squeezing or centrifuging, a small volume of pore water, 100 ??L, was taken for analysis by electrospray ionization-mass spectrometry. Porewater samples were analyzed directly without filtration or fractionation, in positive and negative mode, for polar organic compounds. Spectra in both modes were dominated by low-molecular-weight ions. Negative mode had clusters of ions differing by -60 daltons, possibly due to increasing concentrations of inorganic salts. The numberaverage molecular weight and weight-average molecular weight values for the pore waters from the Chesapeake Bay impact structure are higher than those reported for other aquatic sources of natural dissolved organic carbon as determined by electrospray ionization-mass spectrometry. In order to address the question of whether drilling mud fluids may have contaminated the pore waters during sample collection, spectra from the pore waters were compared to spectra from drilling mud fluids. Ions indicative of drilling mud fluids were not found in spectra from the pore waters, indicating there was no detectable contamination, and highlighting the usefulness of this analytical technique for detecting potential contamination during sample collection. ?? 2009 The Geological Society of America.

  1. Relocation of carbon from decomposition of {sup 14}C-labelled needle and fine root litter in peat soil

    Energy Technology Data Exchange (ETDEWEB)

    Domish, T.; Laine, J.; Laiho, R. [Helsinki Univ. (Finland). Dept. of Forest Ecology; Finer, L. [Finnish Forest Research Inst. (Finland). Joensuu Research Station; Karsisto, M. [Finnish Forest Research Inst. (Finland). Dept. of Forest Ecology

    1996-12-31

    Drainage of peatlands promotes a shift of biomass and production from the ground vegetation to the trees. Thus, the above-ground (e.g. needles) and below-ground (roots) litter production of trees increases. Fine roots in particular are an important factor in the carbon and nutrient cycle in forest ecosystems. A major part of the annual net primary production of trees may be allocated below ground, the relative proportion being smaller on fertile sites than on less fertile ones. For modelling the carbon balance of drained peatlands, it is important to know the fate of carbon from newly introduced and decomposing litter. Newly added and fertilised tree litter material may be decomposed at a rate different than litter from the ground vegetation. The objectives of this study are to study the pathways of decomposing litter carbon in peat soil and to evaluate the use of the litterbag method in a controlled environment. (9 refs.)

  2. On the isolation of elemental carbon for micro-molar 14C accelerator mass spectrometry; evaluation of alternative isolation procedures, and accuracy assurance using a hybrid isotopic particulate carbon reference material

    Directory of Open Access Journals (Sweden)

    L. A. Currie

    2005-05-01

    Full Text Available The primary objective of the research reported here has been the development of an hybrid reference material (RM to serve as a test of accuracy for elemental carbon (EC isotopic (14C speciation measurements. Such measurements are critically important for the quantitative apportionment of fossil and biomass sources of ''soot'' (EC, the tracer of fire that has profound effects on health, atmospheric visibility, and climate. Previous studies of 14C-EC measurement quality, carried out with NIST SRM 1649a (Urban Dust, showed a range of results, but since the ''truth'' was not known for this natural matrix RM, one had to rely on isotopic-chemical consistency evidence (14C in PAH, EC of measurement validity (Currie et al., 2002. Components of the new Hybrid RM (DiesApple, however, have known 14C and EC composition, and they are nearly orthogonal (isotopically and chemically. NIST SRM 2975 (Forklift Diesel Soot has little or no 14C, and its major compositional component is EC. SRM 1515 (Apple Leaves has the 14C content of biomass-C, and it has little or no EC. Thus, the hybrid RM can serve as an absolute isotopic test for the absence of EC-mimicking pyrolysis-C from SRM 1515 in the EC isolate of the hybrid RM, together with testing for conservation of its dominant soot fraction through the isolation procedure.

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

    Directory of Open Access Journals (Sweden)

    Kinya Sakanishi

    2012-05-01

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

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

    Science.gov (United States)

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

    2015-12-01

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

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

    Science.gov (United States)

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

    2015-04-01

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

  6. Granular activated carbon for simultaneous adsorption and biodegradation of toxic oil sands process-affected water organic compounds.

    Science.gov (United States)

    Islam, Md Shahinoor; Zhang, Yanyan; McPhedran, Kerry N; Liu, Yang; Gamal El-Din, Mohamed

    2015-04-01

    Naphthenic acids (NAs) released into oil sands process-affected water (OSPW) during bitumen processing in Northern Alberta are problematic for oil sands industries due to their toxicity in the environment and resistance to degradation during conventional wastewater treatment processes. Granular activated carbon (GAC) has shown to be an effective media in removing biopersistent organics from wastewater using a combination of adsorption and biodegradation removal mechanisms. A simultaneous GAC (0.4 g GAC/L) adsorption and biodegradation (combined treatment) study was used for the treatment of raw and ozonated OSPW. After 28 days of batch treatment, classical and oxidized NAs removals for raw OSPW were 93.3% and 73.7%, and for ozonated OSPW were 96.2% and 77.1%, respectively. Synergetic effects of the combined treatment process were observed in removals of COD, the acid extractable fraction, and oxidized NAs, which indicated enhanced biodegradation and bioregeneration in GAC biofilms. A bacteria copy number >10(8) copies/g GAC on GAC surfaces was found using quantitative real time polymerase chain reaction after treatment for both raw and ozonated OSPW. A Microtox(®) acute toxicity test (Vibrio fischeri) showed effective toxicity removal (>95.3%) for the combined treatments. Therefore, the simultaneous GAC adsorption and biodegradation treatment process is a promising technology for the elimination of toxic OSPW NAs.

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

    Science.gov (United States)

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

    2016-06-01

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

  8. Influence of Co substitution on magnetoelastic properties of Er{sub 2}Fe{sub 14-x}Co{sub x}B (x = 1, 3 and 5) intermetallic compounds

    Energy Technology Data Exchange (ETDEWEB)

    Khoshnoud, D. Sanavi [Faculty of Science, Department of Physics, Ferdowsi University of Mashhad, Mashhad, Khorasan Razavi (Iran, Islamic Republic of); Tajabor, N. [Faculty of Science, Department of Physics, Ferdowsi University of Mashhad, Mashhad, Khorasan Razavi (Iran, Islamic Republic of)], E-mail: tajabor@ferdowsi.um.ac.ir; Fruchart, D.; Gignoux, D.; Miraglia, S. [Institut. Neel, Departement MCMF, Groupe IICF, BP 166, 38042 Grenoble Cedex 9 (France); Pourarian, F. [Department of Material Science and Engineering, Carengie Mellon University, Pittsburgh, PA 15219 (United States)

    2009-07-08

    The magnetostriction and thermal expansion of Er{sub 2}Fe{sub 14-x}Co{sub x}B (x = 1, 3 and 5) intermetallic compounds were measured, using the strain gauge method in the temperature range 75-450 K under applied magnetic fields up to 1.5 T. For all samples the longitudinal magnetostriction ({lambda}{sub l}) undergoes an anomaly around the spin reorientation temperature (T{sub SR}). It is also observed that {lambda}{sub l} decreases with increasing the Co content. All compounds show saturation type behaviour in their anisotropic magnetostriction curves at different temperatures and applied fields. The saturation behaviour of the compound with x = 3 occurs at higher temperatures than with x = 1 and 5. The volume magnetostriction strongly increases below {mu}{sub 0}H = 0.3 T, then monotonically rises with applied field up to the spin reorientation temperature. An invar type behaviour is observed above 200 K in the compound with x = 1. The results are discussed based on the temperature dependence of magnetocrystalline anisotropy of compounds below and above their T{sub SR}.

  9. Priming in permafrost soils: High vulnerability of arctic soil organic carbon to increased input of plant-derived compounds

    Science.gov (United States)

    Wild, Birgit; Gentsch, Norman; Capek, Petr; Diakova, Katerina; Alves, Ricardo; Barta, Jiri; Gittel, Antje; Guggenberger, Georg; Lashchinskiy, Nikolay; Knoltsch, Anna; Mikutta, Robert; Santruckova, Hana; Schnecker, Jörg; Shibistova, Olga; Takriti, Mounir; Urich, Tim; Watzka, Margarete; Richter, Andreas

    2015-04-01

    Arctic ecosystems are warming rapidly, resulting in a stimulation of both plant primary production and soil organic matter (SOM) decomposition. In addition to this direct stimulation, SOM decomposition might also be indirectly affected by rising temperatures mediated by the increase in plant productivity. Higher root litter production for instance might decrease SOM decomposition by providing soil microorganisms with alternative C and N sources ("negative priming"), or might increase SOM decomposition by facilitating microbial growth and enzyme production ("positive priming"). With about 1,700 Pg of organic C stored in arctic soils, and 88% of that in horizons deeper than 30 cm, it is crucial to understand the controls on SOM decomposition in different horizons of arctic permafrost soils, and thus the vulnerability of SOM to changes in C and N availability in a future climate. We here report on the vulnerability of SOM in arctic permafrost soils to an increased input of plant-derived organic compounds, and on its variability across soil horizons and sites. We simulated an increased input of plant-derived compounds by amending soil samples with 13C-labelled cellulose or protein, and compared the mineralization of native, unlabelled soil organic C (SOC) to unamended control samples. Our experiment included 119 individual samples of arctic permafrost soils, covering four sites across the Siberian Arctic, and five soil horizons, i.e., organic topsoil, mineral topsoil, mineral subsoil and cryoturbated material (topsoil material buried in the subsoil by freeze-thaw processes) from the active layer, as well as thawed material from the upper permafrost. Our findings suggest that changes in C and N availability in Arctic soils, such as mediated by plants, have a high potential to alter the decomposition of SOM, but also point at fundamental differences between soil horizons. In the organic topsoil, SOC mineralization increased by 51% after addition of protein, but was not

  10. Lithology, fault displacement, and origin of secondary calcium carbonate and opaline silica at Trenches 14 and 14D on the Bow Ridge Fault at Exile Hill, Nye County, Nevada

    International Nuclear Information System (INIS)

    Yucca Mountain, a proposed site for a high-level nuclear-waste repository, is located in southern Nevada, 20 km east of Beatty, and adjacent to the southwest comer of the Nevada Test Site (NTS) (fig. 1). Yucca Mountain is located within the Basin and Range province of the western United States. The climate is semiarid, and the flora is transitional between that of the Mojave Desert to the south and the Great Basin Desert to the north. As part of the evaluation, hydrologic conditions, especially water levels, of Yucca Mountain and vicinity during the Quaternary, and especially the past 20,000 years, are being characterized. In 1982, the US Geological Survey, in cooperation with the US Department of Energy (under interagency agreement DE-A104-78ET44802), excavated twenty-six bulldozer and backhoe trenches in the Yucca Mountain region to evaluate the nature and frequency of Quaternary faulting (Swadley and others, 1984). The trenches were oriented perpendicular to traces of suspected Quaternary faults and across projections of known bedrock faults into Quaternary deposits. Trench 14 exposes the Bow Ridge Fault on the west side of Exile Hill. Although the original purpose of the excavation of trench 14 was to evaluate the nature and frequency of Quaternary faulting on the Bow Ridge Fault, concern arose as to whether or not the nearly vertical calcium carbonate (the term ''carbonate'' in this study refers to calcium carbonate) and opaline silica veins in the fault zone were deposited by ascending waters (ground water). These veins resemble in gross morphology veins commonly formed by hydrothermal processes

  11. The applicability of C-14 measurements in the soil gas for the assessment of leakage out of underground carbon dioxide reservoirs

    Directory of Open Access Journals (Sweden)

    Chałupnik Stanisław

    2014-03-01

    Full Text Available Poland, due to the ratification of the Kioto Protocol, is obliged to diminish the emission of greenhouse gases. One of the possible solutions of this problem is CO2 sequestration (CCS - carbon capture and storage. Such an option is a priority in the European Union. On the other hand, CO2 sequestration may be potentially risky in the case of gas leakage from underground reservoirs. The most dangerous event may be a sudden release of the gas onto the surface. Therefore, it is very important to know if there is any escape of CO2 from underground gas reservoirs, created as a result of sequestration. Such information is crucial to ensure safety of the population in areas located above geological reservoirs. It is possible to assess the origin of carbon dioxide, if the measurement of radiocarbon 14C concentration in this gas is done. If CO2 contains no 14C, it means, that the origin of the gas is either geological or the gas has been produced as a result of combustion of fossil fuels, like coal. A lot of efforts are focused on the development of monitoring methods to ensure safety of CO2 sequestration in geological formations. A radiometric method has been tested for such a purpose. The main goal of the investigations was to check the application possibility of such a method. The technique is based on the liquid scintillation counting of samples. The gas sample is at first bubbled through the carbon dioxide adsorbent, afterwards the adsorbent is mixed with a dedicated cocktail and measured in a low-background liquid scintillation spectrometer Quantulus. The described method enables measurements of 14C in mine and soil gas samples.

  12. Carbon-14 in tree rings and other terrestrial samples in the vicinity of Ignalina Nuclear Power Plant, Lithuania

    Energy Technology Data Exchange (ETDEWEB)

    Mazeika, Jonas [Radioisotope Research Laboratory, Institute of Geology and Geography, T. Sevcenkos 13, LT-03223 Vilnius (Lithuania)], E-mail: mazeika@geo.lt; Petrosius, Rimantas [Radioisotope Research Laboratory, Institute of Geology and Geography, T. Sevcenkos 13, LT-03223 Vilnius (Lithuania); Pukiene, Rutile [Dendroclimatology and Radiometrics Group, Vytautas Magnus University, Z.E. Zilibero 6, LT-46324 Kaunas (Lithuania)], E-mail: r.pukiene@gmf.vdu.lt

    2008-02-15

    The results of {sup 14}C measurements in the annual tree rings from the Ignalina Nuclear Power Plant (INPP) surroundings, Lithuania, for the period of its operation from 1984 to 2002 are presented. The terrestrial samples, mainly moss and related soil, are studied in places as well. The tree rings have shown slightly enhanced {sup 14}C activity due to operation of the nuclear power plant. The maximal calculated normalized {sup 14}C release of 11 TBq GW{sub e}{sup -1} year{sup -1} and the maximal effective dose of 2.0 x 10{sup -3} mSv year{sup -1} resulting from the {sup 14}C were estimated for 1999. For other years of INPP operation these values are lower. The excess of {sup 14}C specific activity measured in the moss and soil samples from moss-covered sites near the nuclear power plant (up to 0.5 km) showed highly elevated {sup 14}C contents (up to 813 pMC), probably indicating releases of particulate material.

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

    Directory of Open Access Journals (Sweden)

    Fortune Ezemobi

    2014-12-01

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

  14. Photoperiodic effects on short-pulse 14C assimilation and overall carbon and nitrogen allocation patterns in contrasting quinoa cultivars

    DEFF Research Database (Denmark)

    Bendevis, Mira Arpe; Sun, Yujie; Rosenqvist, Eva;

    2014-01-01

    photoperiod neutral cv. 'Titicaca' were studied under short (10h) and long (17.5h) days, with respect to C and N distribution as well as partitioning of newly assimilated C to plant organs. An extended photoperiod resulted in 14C decreasingly being allocated to stem growth and lower leaves in 'Titicaca', but...... an immediate increase in carbon allocation to upper leaves, and over time to the reproductive structures, resulting in a more than 50% increase in final yield. Collectively the results indicate that even though the photoperiod sensitive cultivar flowered under long photoperiod it did not develop...

  15. Influence of atmospheric 14CO2 on determination of the ratio of biogenic carbon to fossil one in exhaust gases using accelerator mass spectrometry. Experimental evaluation for industrial flue gases

    International Nuclear Information System (INIS)

    The influence of atmospheric 14CO2 was evaluated on the determination of biogenic carbon ratios in industrial flue gases using accelerated mass spectrometry(AMS). Bioethanol, n-hexane, and their mixtures were combusted with a four-stroke engine, and 14CO2 in exhaust gases was analyzed by AMS. The experimental biogenic carbon ratio determined by ASTM D6866 method was 1.2 times higher than the theoretical value of mixed fuel containing 3.18% biogenic carbons. In general, the influence of atmospheric 14CO2 taken in combustion gases is neglected. It seems that the error cannot be neglected under international trading of emission allowances, where a large amount of carbons in the fuel were evaluated. The experimental value became to be the theoretical value by subtracting the amount of atmospheric 14C from that of the samples. As the contents of biofuel increased, the experimental biogenic carbon ratios reached the theoretical values and the influence of atmospheric 14CO2 decreased. We recommend that the influence of atmospheric 14CO2 should be corrected when fuel samples contain low amounts of 14C. (author)

  16. Syntheses and properties of a family of new compounds RE{sub 3}Sb{sub 3}Co{sub 2}O{sub 14} (RE=La, Pr, Nd, Sm–Ho) with an ordered pyrochlore structure

    Energy Technology Data Exchange (ETDEWEB)

    Li, Kuo; Hu, Yufei [Beijing National Laboratory for Molecular Sciences, State Key Laboratory of Rare Earth Materials Chemistry and Applications, College of Chemistry and Molecular Engineering, Peking University, Beijing 100871 (China); Wang, Yingxia, E-mail: Wangyx@pku.edu.cn [Beijing National Laboratory for Molecular Sciences, State Key Laboratory of Rare Earth Materials Chemistry and Applications, College of Chemistry and Molecular Engineering, Peking University, Beijing 100871 (China); Kamiyama, Takashi [Institute of Materials Structure Science, High Energy Accelerator Research Organization, Tsukuba, Ibaraki 305-0801 (Japan); Wang, Bingwu; Li, Zhaofei [Beijing National Laboratory for Molecular Sciences, State Key Laboratory of Rare Earth Materials Chemistry and Applications, College of Chemistry and Molecular Engineering, Peking University, Beijing 100871 (China); Lin, Jianhua, E-mail: jhlin@pku.edu.cn [Beijing National Laboratory for Molecular Sciences, State Key Laboratory of Rare Earth Materials Chemistry and Applications, College of Chemistry and Molecular Engineering, Peking University, Beijing 100871 (China)

    2014-09-15

    Isostructural compounds RE{sub 3}Sb{sub 3}Co{sub 2}O{sub 14} (RE=La, Pr, Nd, Sm–Ho) with an ordered pyrochlore structure were synthesized. The structure of La{sub 3}Sb{sub 3}Co{sub 2}O{sub 14} was solved ab initio based on powder XRD data, and refined by combining with high resolution neutron diffraction data. La{sub 3}Sb{sub 3}Co{sub 2}O{sub 14} crystallizes in the space group R-3m with the unit cell parameters a=7.52954(2) Å and c=17.59983(6) Å. The structures of other members in this family are confirmed by Rietveld refinement using powder X-ray diffraction data. The cations (RE, Sb and Co) in RE{sub 3}Sb{sub 3}Co{sub 2}O{sub 14} are orderly distributed, presenting as [RE{sub 3}Co][Sb{sub 3}Co]O{sub 14} formula, and giving rise to two distinctive Kagome lattices constructed by RE{sup 3+} and Sb{sup 5+}, respectively. Co{sup 2+} occupies 8-coordinated and 6-coordinated environments, showing low spin (S=1/2) and high spin (S=3/2) states respectively. The magnetic susceptibility and UV–visual spectroscopy supports the magnetic observation. TDDFT calculation was performed to interpret the electronic states. The compounds [RE{sub 3}Co][Sb{sub 3}Co]O{sub 14} provide a profound example in which the ideal 2D Kagome lattice is derived from the 3D pyrochlore-type structure by an ordered distribution of the metal cations. - Graphical abstract: La{sub 3}Sb{sub 3}Co{sub 2}O{sub 14} crystallizes in a pyrochlore related structure with an ordered distribution of cations, giving rise to two sets of ideal 2D Kagome lattices formed by La{sup 3+} or Sb{sup 5+} respectively. This rhombohedral pyrochlore is a tolerant structure for stable compounds composed by many light rare-earth and d-transition elements. Substituting Zn{sup 2+} or Mg{sup 2+} for Co{sup 2+} will provide a series of compounds useful for studying magnetic interactions in the rare-earth Kagome lattices. - Highlights: • Pyrochlore-type La{sub 3}Sb{sub 3}Co{sub 2}O{sub 14} shows an ordered distribution of

  17. Assessment of a ground water flow model of the Bangkok Basin, Thailand, using carbon-14-based ages and paleohydrology

    Science.gov (United States)

    Sanford, W.E.; Buapeng, S.

    1996-01-01

    A study was undertaken to understand the groundwater flow conditions in the Bangkok Basin, Thailand, by comparing 14C-based and simulated groundwater ages. 14C measurements were made on about 50 water samples taken from wells throughout the basin. Simulated ages were obtained using 1) backward-pathline tracking based on the well locations, and 2) results from a three-dimensional groundwater flow model. Comparisons of ages at these locations reveal a large difference between 14C-based ages and ages predicted by the steady-state groundwater flow model. Mainly, 14C and 13C analyses indicate that groundwater in the Bangkok area is about 20,000 years old, whereas steady-state flow and transport simulations imply that groundwater in the Bangkok area is 50,000-100,000 years old. One potential reason for the discrepancy between simulated and 14C-based ages is the assumption in the model of steady-state flow. Groundwater velocities were probably greater in the region before about 10,000 years ago, during the last glacial maximum, because of the lower position of sea level and the absence of the surficial Bangkok Clay. Paleoflow conditions were estimated and then incorporated into a second set of simulations. The new assumption was that current steady-state flow conditions existed for the last 8,000 years but were preceded by steady-state conditions representative of flow during the last glacial maximum. This "transient" paleohydrologic simulation yielded a mean simulated age that more closely agrees with the mean 14C-based age, especially if the 14C-based age is corrected for diffusion into clay layers. Although the uncertainties in both the simulated and 14C-based ages are nontrivial, the magnitude of the improved match in the mean age using a paleohydrologic simulation instead of a steady-state simulation suggests that flow conditions in the basin have changed significantly over the last 10,000-20,000 years. Given that the valid age range of 14C-dating methods and the

  18. Understanding the Mechanisms Enabling an Ultra-high Efficiency Moving Wire Interface for Real-time Carbon 14 Accelerator Mass Spectrometry Quantitation of Samples Suspended in Solvent

    Science.gov (United States)

    Thomas, Avraham Thaler

    Carbon 14 (14C) quantitation by accelerator mass spectrometry (AMS) is a powerfully sensitive and uniquely quantitative tool for tracking labeled carbonaceous molecules in biological systems. This is due to 14C's low natural abundance of 1 ppt, the nominal difference in biological activity between an unlabeled and a 14C-labeled molecule, and the ability of AMS to measure isotopic ratios independently of a sample's other characteristics. To make AMS more broadly accessible, a moving wire interface for real-time coupling of high pressure liquid chromatography (HPLC) to AMS and high throughput AMS quantitation of minute single samples has been developed. Prior to this work, samples needed to be converted to solid carbon before measurement. This conversion process has many steps and requires that the sample size be large enough to allow precise handling of the resulting graphite. These factors make the process susceptible to error and time consuming, as well as requiring 0.5 ug of carbon. Samples which do not contain enough carbon, such as HPLC fractions, must be bulked up. This adds background and increases effort. The moving wire interface overcomes these limitations by automating sample processing. Samples placed on the wire are transported through a solvent removal stage followed by a combustion stage after which the combustion products are directed to a gas accepting ion source. The ion source converts the carbon from the CO2 combustion product into C ions, from which an isotopic ratio can be determined by AMS. Although moving wire interfaces have been implemented for various tasks since 1964, the efficiency of these systems at transferring fluid from an HPLC to the wire was only 3%, the efficiency of transferring combustion products from the combustion oven to ion source was only 30%, the flow and composition of the carrier gas from the combustion oven to the ion source needed to be optimized for coupling to an AMS gas accepting ion source and the drying ovens

  19. Carbon cycle dynamics and solar activity embedded in a high-resolution 14C speleothem record from Belize, Central America

    Science.gov (United States)

    Lechleitner, Franziska A.; Breitenbach, Sebastian F. M.; McIntyre, Cameron; Asmerom, Yemane; Prufer, Keith M.; Polyak, Victor; Culleton, Brendan J.; Kennett, Douglas J.; Eglinton, Timothy I.; Baldini, James U. L.

    2015-04-01

    Speleothem 14C has recently emerged as a potentially powerful proxy for climate reconstruction. Several studies have highlighted the link between karst hydrology and speleothem 14C content, and a number of possible causes for this relationship have been proposed, such as dripwater flow dynamics in the karst and changes in soil organic matter (SOM) turnover time (e.g. Griffiths et al., 2012). Here we present a high resolution 14C record for a stalagmite (YOK-I) from Yok Balum cave in southern Belize, Central America. YOK-I grew continuously over the last 2000 years, and has been dated very precisely with the U-Th method (40 dates, mean uncertainty ventilation and hydrologic resilience to seismic activity, Journal of Cave and Karst Studies

  20. Autoradiographic study on the incorporation of carbon-14 labeled formate and adenine into nucleic acid in blood-forming cells

    International Nuclear Information System (INIS)

    The incorporation of [14C]formate and [8-14C]adenine into nucleic acid in blood-forming cells was studied by the autoradiographic technique. The isotopic markers were injected subcutaneously into young rats weighting from 100 to 150 g three times every 24 hours and the animals were examined 3 hours after the last injection. In the case of [14C]formate injection, erythroblasts exhibited extremely strong labeling in contrast to weaker labeling of other blood-forming cells. In the case of [14C]adenine administration, on the other hand, immature cells of the granuclocytic series as well as immature reticulum cells (proliferating cells of reticular tissue) were much more heavily labeled than were other blood-forming cells, particularly the erythroblasts which revealed weak or no labeling. By digestion or extraction of DNA, RNA or both from cells with DNase, RNase or hot 10% perchloric acid treatment, respectively, it was confirmed that the observed heavy labeling of any type of cells with either [14C]formate or [14C]adenine was due chiefly to incorporation of the radioactive materials into nuclear DNA. The present results are discussed together with the findings of earlier studies on lymphoid cells which indicate that, in certain cell types, the patterns of [3H]deoxycytidine labeling differ considerably from the corresponding patterns of [3H]deoxycytidine labeling. The present and earlier findings provide evidence to substantiate that, among blood-forming cells, there are considerable variations in the labeling patterns of nuclear DNA depending on differences in the radioactive DNA precursors used as well as in the cell types. (author)

  1. Bacterial decomposition of synthetic 14C-labeled lignin and lignin monomer derivatives

    International Nuclear Information System (INIS)

    Nocardia sp. which was isolated from soil is capable of degrading synthetic lignin and utilizing its monomer derivatives. Decomposition was monitored by measuring the 14CO2 evolved and O2 consumed, when the bacterium was grown on a medium containing specifically 14C-labeled lignins or monomer phenolic compounds as major carbon source. The time course of the 14CO2 release and O2 uptake indicates a significant depolymerization and utilization of lignin by the Nocardia sp. (author)

  2. Comment on: Comment on ''Mysterious abrupt carbon-14 increase in coral contributed by a come'' Yi Liu et al

    CERN Document Server

    Melott, Adrian L

    2014-01-01

    Unfortunately, Liu et al. contains a number of errors and omissions which compromise its conclusions. These have to do with the amount of 14C which is necessary to deposit in the atmosphere in order to see a perturbation like that in 774 AD, and the ability of a comet to do so.

  3. Synthesis, crystal structure and luminescent properties of one new inorganic-organic hybrid compound [O 2NBzQL] 4[Cd(SCN) 4(NCS) 2] (O 2NBzQL = 1-(4'-NO 2-benzyl)quinolinium cation)

    Science.gov (United States)

    Bai, Yan; Hu, Xue-Fu; Dang, Dong-Bin; Bi, Feng-Lei; Niu, Jing-Yang

    2011-01-01

    A new inorganic-organic hybrid compound [O 2NBzQL] 4[Cd(SCN) 4(NCS) 2] (O 2NBzQL = 1-(4'-NO 2-benzyl)quinolinium cation) has been synthesized and characterized by IR, UV, elemental analysis and X-ray crystallography. Cd(II) atom has an distorted octahedral environment with an N 4S 2 donor set. In solid state there are three types of face-to-face π-π interactions between adjacent cations and multiform C-H⋯S and C-H⋯N hydrogen bonds between [O 2NBzQL] + cations and cadmium thiocyanate anions. The luminescent properties of the title compound were both investigated in H 2O solution and in solid state at room temperature, respectively.

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

    Energy Technology Data Exchange (ETDEWEB)

    Queiroz, Carlos Alberto da Silva

    1996-05-01

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

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

    Science.gov (United States)

    Sheng, G D; Shao, D D; Ren, X M; Wang, X Q; Li, J X; Chen, Y X; Wang, X K

    2010-06-15

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

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

    Science.gov (United States)

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

    2014-12-01

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

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

    Institute of Scientific and Technical Information of China (English)

    杨明; 金效齐

    2016-01-01

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

  8. AccR is a master regulator involved in carbon catabolite repression of the anaerobic catabolism of aromatic compounds in Azoarcus sp. CIB.

    Science.gov (United States)

    Valderrama, J Andrés; Shingler, Victoria; Carmona, Manuel; Díaz, Eduardo

    2014-01-24

    Here we characterized the first known transcriptional regulator that accounts for carbon catabolite repression (CCR) control of the anaerobic catabolism of aromatic compounds in bacteria. The AccR response regulator of Azoarcus sp. CIB controls succinate-responsive CCR of the central pathways for the anaerobic catabolism of aromatics by this strain. Phosphorylation of AccR to AccR-P triggers a monomer-to-dimer transition as well as the ability to bind to the target promoter and causes repression both in vivo and in vitro. Substitution of the Asp(60) phosphorylation target residue of the N-terminal receiver motif of AccR to a phosphomimic Glu residue generates a constitutively active derivative that behaves as a superrepressor of the target genes. AccR-P binds in vitro to a conserved inverted repeat (ATGCA-N6-TGCAT) present at two different locations within the PN promoter of the bzd genes for anaerobic benzoate degradation. Because the DNA binding-proficient C-terminal domain of AccR is monomeric, we propose an activation mechanism in which phosphorylation of Asp(60) of AccR alleviates interdomain repression mediated by the N-terminal domain. The presence of AccR-like proteins encoded in the genomes of other β-proteobacteria of the Azoarcus/Thauera group further suggests that AccR constitutes a master regulator that controls anaerobic CCR in these bacteria. PMID:24302740

  9. AccR Is a Master Regulator Involved in Carbon Catabolite Repression of the Anaerobic Catabolism of Aromatic Compounds in Azoarcus sp. CIB*

    Science.gov (United States)

    Valderrama, J. Andrés; Shingler, Victoria; Carmona, Manuel; Díaz, Eduardo

    2014-01-01

    Here we characterized the first known transcriptional regulator that accounts for carbon catabolite repression (CCR) control of the anaerobic catabolism of aromatic compounds in bacteria. The AccR response regulator of Azoarcus sp. CIB controls succinate-responsive CCR of the central pathways for the anaerobic catabolism of aromatics by this strain. Phosphorylation of AccR to AccR-P triggers a monomer-to-dimer transition as well as the ability to bind to the target promoter and causes repression both in vivo and in vitro. Substitution of the Asp60 phosphorylation target residue of the N-terminal receiver motif of AccR to a phosphomimic Glu residue generates a constitutively active derivative that behaves as a superrepressor of the target genes. AccR-P binds in vitro to a conserved inverted repeat (ATGCA-N6-TGCAT) present at two different locations within the PN promoter of the bzd genes for anaerobic benzoate degradation. Because the DNA binding-proficient C-terminal domain of AccR is monomeric, we propose an activation mechanism in which phosphorylation of Asp60 of AccR alleviates interdomain repression mediated by the N-terminal domain. The presence of AccR-like proteins encoded in the genomes of other β-proteobacteria of the Azoarcus/Thauera group further suggests that AccR constitutes a master regulator that controls anaerobic CCR in these bacteria. PMID:24302740

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

    Science.gov (United States)

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

    2016-09-01

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

  11. Carbon isotope (δ13C) excursions suggest times of major methane release during the last 14 ka in Fram Strait, the deep-water gateway to the Arctic

    Science.gov (United States)

    Consolaro, C.; Rasmussen, T. L.; Panieri, G.; Mienert, J.; Bünz, S.; Sztybor, K.

    2014-10-01

    We present results from a sediment core collected from a pockmark field on the Vestnesa Ridge (∼80° N) in the eastern Fram Strait. This is the only deep-water gateway to the Arctic, and one of the northernmost marine gas hydrate provinces in the world. Eight 14C AMS dating reveals a detailed chronology for the last 14 ka BP. The δ13C record measured on the benthic foraminiferal species Cassidulina neoteretis shows two distinct intervals with negative values, as low as -4.37‰ in the Bølling-Allerød interstadials and as low as -3.41‰ in the early Holocene. After cleaning procedure designed to remove all authigenic carbonate coatings on benthic foraminiferal tests, the 13C values are still negative (as low as -2.75‰). We have interpreted these negative carbon isotope excursions (CIEs) to record past methane release events, resulting from the incorporation of 13C-depleted carbon from methane emissions into the benthic foraminiferal shells. The CIEs during the Bølling-Allerød interstadials and the early Holocene relate to periods of ocean warming, sea level rise and increased concentrations of methane (CH4) in the atmosphere. CIEs with similar timing have been reported from other areas in the North Atlantic suggesting a regional event. The trigger mechanisms for such regional events remain to be determined. We speculate that sea-level rise and seabed loading due to high sediment supply in combination with increased seismic activity as a result of rapid deglaciation may have triggered the escape of significant amounts of methane to the seafloor and the water column above.

  12. Carbon isotope (δ13C excursions suggest times of major methane release during the last 14 ka in Fram Strait, the deep-water gateway to the Arctic

    Directory of Open Access Journals (Sweden)

    C. Consolaro

    2014-10-01

    Full Text Available We present results from a sediment core collected from a pockmark field on the Vestnesa Ridge (∼80° N in the eastern Fram Strait. This is the only deep-water gateway to the Arctic, and one of the northernmost marine gas hydrate provinces in the world. Eight 14C AMS dating reveals a detailed chronology for the last 14 ka BP. The δ13C record measured on the benthic foraminiferal species Cassidulina neoteretis shows two distinct intervals with negative values, as low as −4.37‰ in the Bølling–Allerød interstadials and as low as −3.41‰ in the early Holocene. After cleaning procedure designed to remove all authigenic carbonate coatings on benthic foraminiferal tests, the 13C values are still negative (as low as −2.75‰. We have interpreted these negative carbon isotope excursions (CIEs to record past methane release events, resulting from the incorporation of 13C-depleted carbon from methane emissions into the benthic foraminiferal shells. The CIEs during the Bølling–Allerød interstadials and the early Holocene relate to periods of ocean warming, sea level rise and increased concentrations of methane (CH4 in the atmosphere. CIEs with similar timing have been reported from other areas in the North Atlantic suggesting a regional event. The trigger mechanisms for such regional events remain to be determined. We speculate that sea-level rise and seabed loading due to high sediment supply in combination with increased seismic activity as a result of rapid deglaciation may have triggered the escape of significant amounts of methane to the seafloor and the water column above.

  13. Comparison of the efficacy of biodegradable and non-biodegradable scintillation liquids on the counting of tritium- and [14C]-labeled compounds

    Directory of Open Access Journals (Sweden)

    Medeiros R.B.

    2003-01-01

    Full Text Available The widespread use of ³H and 14C in research has generated a large volume of waste mixed with scintillation liquid, requiring an effective control and appropriate storage of liquid radioactive waste. In the present study, we compared the efficacy of three commercially available scintillation liquids, Optiphase HiSafe 3, Ultima-Gold(TM AB (biodegradable and Insta-Gel-XF (non-biodegradable, in terms of [14C]-glucose and [³H]-thymidine counting efficiency. We also analyzed the effect of the relative amount of water (1.6 to 50%, radioisotope concentration (0.1 to 100 nCi/ml, pH (2 to 10 and color of the solutions (samples containing 0.1 to 1.0 mg/ml of Trypan blue on the counting efficiency in the presence of these scintillation liquids. There were few significant differences in the efficiency of 14C and ³H counting obtained with biodegradable or non-biodegradable scintillation liquids. However, there was an 83 and 94% reduction in the efficiency of 14C and ³H counting, respectively, in samples colored with 1 mg/ml Trypan blue, but not with 0.1 mg/ml, independent of the scintillation liquid used. Considering the low cost of biodegradable scintillation cocktails and their efficacy, these results show that traditional hazardous scintillation fluids may be replaced with the new safe biodegradable fluids without impairment of ³H and 14C counting efficiency. The use of biodegradable scintillation cocktails minimizes both human and environmental exposure to hazardous solvents. In addition, some biodegradable scintillation liquids can be 40% less expensive than the traditional hazardous cocktails.

  14. Carbon-14-ochratoxin A distribution in the Japanese quail (Coturnix coturnix japonica) monitored by whole body autoradiography

    Energy Technology Data Exchange (ETDEWEB)

    Fuchs, R.; Appelgren, L.E.; Hagelberg, S.; Hult, K.

    1988-05-01

    Tissue distribution of the nephrotoxic mycotoxin ochratoxin A was characterized in laying Japanese quail by whole body autoradiography and scintillation counting using /sup 14/C-labelled toxin. Periodically for 8 days after one intravenous injection of 14 microCi/bird, corresponding to 70 ng/g body weight, birds were killed, frozen, and sagittal sections of the whole body were placed on X-ray film. In general, the ochratoxin disappeared from the avian body rapidly. Specific retention of radioactivity was seen as a ring-like distribution in yolks and growing follicles. After sectioning, organs and intestinal contents were removed from carcasses in a frozen condition, homogenized, extracted, chromatographed, and the radioactivity in fractions was measured by scintillation spectroscopy. High concentrations of ochratoxin A were found in gastric intestinal contents, probably originating from toxin excreted in the bile.

  15. The carbon-14 spike in the 8th century was not caused by a cometary impact on Earth

    Science.gov (United States)

    Usoskin, Ilya G.; Kovaltsov, Gennady A.

    2015-11-01

    A mysterious increase of radiocarbon 14 C ca. 775 AD in the Earth's atmosphere has been recently found by Miyake et al. (Miyake, F., Nagaya, K., Masuda, K., Nakamura, T. [2012]. Nature, 486, 240). A possible source of this event has been discussed widely, the most likely being an extreme solar energetic particle event. A new exotic hypothesis has been presented recently by Liu et al. (Liu, Y. [2014]. Sci. Rep., 4, 3728) who proposed that the event was caused by a cometary impact on Earth bringing additional 14 C to the atmosphere. Here we calculated a realistic mass and size of such a comet to show that it would have been huge (≈100 km across and 1017-1020 g of mass) and would have produced a disastrous geological/biological impact on Earth. The absence of an evidence for such a dramatic event makes this hypothesis invalid.

  16. An analytical method for estimating the 14N nuclear quadrupole resonance parameters of organic compounds with complex free induction decays for radiation effects studies

    International Nuclear Information System (INIS)

    The use of 14N nuclear quadrupole resonance (NQR) as a radiation dosimetry tool has only recently been explored. An analytical method for analyzing 14N NQR complex free induction decays is presented with the background necessary to conduct pulsed NQR experiments. The 14N NQR energy levels and possible transitions are derived in step-by-step detail. The components of a pulsed NQR spectrometer are discussed along with the experimental techniques for conducting radiation effects experiments using the spectrometer. Three data analysis techniques -- the power spectral density Fourier transform, state space singular value decomposition (HSVD), and nonlinear curve fitting (using the downhill simplex method of global optimization and the Levenberg-Marquart method) -- are explained. These three techniques are integrated into an analytical method which uses these numerical techniques in this order to determine the physical NQR parameters. Sample data sets of urea and guanidine sulfate data are used to demonstrate how these methods can be employed to analyze both simple and complex free induction decays. By determining baseline values for biologically significant organics, radiation effects on the NQR parameters can be studied to provide a link between current radiation dosimetry techniques and the biological effects of radiation

  17. An analytical method for estimating the {sup 14}N nuclear quadrupole resonance parameters of organic compounds with complex free induction decays for radiation effects studies

    Energy Technology Data Exchange (ETDEWEB)

    Iselin, L.H.

    1992-12-31

    The use of {sup 14}N nuclear quadrupole resonance (NQR) as a radiation dosimetry tool has only recently been explored. An analytical method for analyzing {sup 14}N NQR complex free induction decays is presented with the background necessary to conduct pulsed NQR experiments. The {sup 14}N NQR energy levels and possible transitions are derived in step-by-step detail. The components of a pulsed NQR spectrometer are discussed along with the experimental techniques for conducting radiation effects experiments using the spectrometer. Three data analysis techniques -- the power spectral density Fourier transform, state space singular value decomposition (HSVD), and nonlinear curve fitting (using the downhill simplex method of global optimization and the Levenberg-Marquart method) -- are explained. These three techniques are integrated into an analytical method which uses these numerical techniques in this order to determine the physical NQR parameters. Sample data sets of urea and guanidine sulfate data are used to demonstrate how these methods can be employed to analyze both simple and complex free induction decays. By determining baseline values for biologically significant organics, radiation effects on the NQR parameters can be studied to provide a link between current radiation dosimetry techniques and the biological effects of radiation.

  18. Volatile Organic Compounds (VOCs) and Elevated Concentrations of Carbon Dioxide (CO2) in Unsaturated-Zone Vapors Near a Chemical and Low-Level Radioactivity Waste-Disposal Facility, Amargosa Desert Research Site, Nye County, Nevada

    Science.gov (United States)

    Baker, R. J.; Andraski, B. J.; Walvoord, M. A.; Stonestrom, D. A.; Prudic, D. E.; Luo, W.

    2003-12-01

    As part of its Toxic Substances Hydrology Program, the U.S. Geological Survey is studying contaminant-transport processes in an arid environment at the Amargosa Desert Research Site (http://nevada.usgs.gov/adrs/). The site is near waste-disposal facilities 20 kilometers east of Death Valley National Park. Low-level radioactive waste was buried in unlined trenches of varying depth during 1962-92. Hazardous chemical waste was buried in unlined trenches at an adjacent facility during 1970-88. Mean annual precipitation at the site from 1981 to 2000 was 108 millimeters. The unsaturated zone is aerobic down to the water table, which is about 110 m (meters) deep. Sampling infrastructure south and west of the facility includes a grid of vapor probes 1.5 m deep, a 23.8-m-deep background borehole (JFDB), and two approximately 100-m-deep boreholes (UZB-2 and UZB-3), which are 160 m and 100 m from the nearest trench, respectively, and are instrumented for multi-level sampling. Analytes detected in unsaturated-zone-vapor samples include elevated concentrations of tritium and carbon-14; three chlorofluorocarbon (CFC) compounds, eight chlorinated solvent compounds, and toluene, all at concentrations exceeding 1,000 parts per billion (ppb) in UZB-3, and at lower concentrations in UZB-2 and in the shallow-vapor-probe grid; and CO2 in concentrations up to 2% in UZB-3, whereas maximum CO2 concentrations in JFDB are less than 0.2%. With the notable exception of toluene, VOCs that are known to be highly biodegradable are generally absent or occur at low concentrations (1,000 ppb) in UZB-3 are relatively recalcitrant to biodegradation in this environment. 4. The similarity among their vertical and radial concentration profiles indicates that the same vapor-transport phenomena are responsible for the observed elevated levels of CO2, hydrocarbons, and radionuclides. The CO2- and VOC-concentration data will be used to enhance ongoing efforts to develop process-based models of contaminant

  19. Carbon partitioning in Arabidopsis thaliana is a dynamic process controlled by the plants metabolic status and its circadian clock

    OpenAIRE

    Kölling, Katharina; Thalmann, Matthias; Müller, Antonia; Jenny, Camilla; Zeeman, Samuel C.

    2015-01-01

    Abstract Plant growth involves the coordinated distribution of carbon resources both towards structural components and towards storage compounds that assure a steady carbon supply over the complete diurnal cycle. We used 14CO2 labelling to track assimilated carbon in both source and sink tissues. Source tissues exhibit large variations in carbon allocation throughout the light period. The most prominent change was detected in partitioning towards starch, being low in the morning and more than...

  20. Characterization of Sulfur Compounds in MTBE

    OpenAIRE

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

    2015-01-01

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

  1. Nomenclature on an organic compound (I)

    International Nuclear Information System (INIS)

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

  2. 硫化胶中炭黑品种的粒径分布鉴别方法%Determination of Carbon Black Type in Vulcanized Compound by Particle Size Distribution Analysis

    Institute of Scientific and Technical Information of China (English)

    张翠翠; 苍飞飞; 邹滔; 高原; 马姜; 邓平晔

    2015-01-01

    The relationship between particle size distribution and carbon black type was established and the test method to determine the carbon black type in vulcanized compound was obtained by particle size distribution analysis. The carbon black in the vulcanized compound was recovered by pyrolysis and its particle size distribution was measured by laser diffraction nano-particle size analyzer. The results showed that peak value and standard deviation of different type of carbon black were different and the peak value and standard deviation fluctuated within a small range for the same type of carbon black. Thus the unknown carbon black could be identiifed by measuring its particle size distribution. This identiifcation method was suitable for analysis of carbon black in the vulcanized compound iflled with only one type of carbon black and it could not be applied to blended carbon black and carbon black N774.%探索炭黑粒径分布与炭黑品种之间的关系,建立通过炭黑粒径分布鉴别炭黑品种的方法。通过热裂解法回收硫化胶中的炭黑,将回收的炭黑加入分散剂制成悬浊液,利用纳米激光粒度分布仪进行粒径分布测试。结果表明,不同品种炭黑粒径分布的峰值和标准偏差不同,同种炭黑粒径分布的峰值和标准偏差在一个较小的范围内波动,这是硫化胶中未知炭黑品种鉴别的依据。本方法适用于单一炭黑品种硫化胶分析,不适用于并用炭黑及炭黑N774硫化胶分析。

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

    International Nuclear Information System (INIS)

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

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

    Directory of Open Access Journals (Sweden)

    I. Tolosa

    2013-03-01

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

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

    Institute of Scientific and Technical Information of China (English)

    徐斌; 王雪源

    2012-01-01

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

  6. Itinerant-electron metamagnetism of the Hf{sub 1−x}Ta{sub x}Fe{sub 2} (x=0.125 and 0.14) compounds under high pressure

    Energy Technology Data Exchange (ETDEWEB)

    Diop, L.V.B., E-mail: leopoldbirane@gmail.com [Univ. Grenoble Alpes, Inst NEEL, F-38042 Grenoble (France); CNRS, Inst NEEL, F-38042 Grenoble (France); Arnold, Z. [Institute of Physics AS CR, v.v.i., Na Slovance 2, 182 21 Prague 8 (Czech Republic); Isnard, O. [Univ. Grenoble Alpes, Inst NEEL, F-38042 Grenoble (France); CNRS, Inst NEEL, F-38042 Grenoble (France)

    2015-12-01

    The effect of hydrostatic pressure on the magnetic properties has been investigated for itinerant-electron metamagnetic Hf{sub 1−x}Ta{sub x}Fe{sub 2} (x=0.125 and 0.14) compounds which exhibit a temperature-induced transition from the ferromagnetic (FM) to the antiferromagnetic (AFM) state upon heating. Both the magnetic transition temperature T{sub FM–AFM} and the spontaneous magnetization M{sub S} decreases with increasing pressure. The application of an external pressure leads also to the strong increase of the AFM–FM transition field μ{sub 0}H{sub cr}. The magnitude of the pressure coefficient, dln(T{sub FM–AFM})/dP, is much larger than that of dln(M{sub S})/dP. This extremely large difference between the pressure coefficients is explained by the influence of spin fluctuations on the magnetovolume effects in the compounds Hf{sub 0.875}Ta{sub 0.125}Fe{sub 2} and Hf{sub 0.86}Ta{sub 0.14}Fe{sub 2}. - Highlights: • The effect of hydrostatic pressure on the magnetic properties is presented. • A field-induced AFM–FM transition between has been observed. • |dln(T{sub FM–AFM})/dP|is one order of magnitude larger than |dln(M{sub S})/dP|. • The AFM–FM transition field increases strongly with external pressure.

  7. Impact of UV-B radiation on photosynthetic assimilation of 14C-bicarbonate and inorganic 15N-compounds by cyanobacteria

    International Nuclear Information System (INIS)

    The cyanobacteria Anabaena cylindrica and Synechococcus leopoliensis (=Anacystis nidulans) were grown at different levels of UV-B radiation (439, 717, 1230 and 1405 J m-2d-1, weighted according Caldwell, 1971) for 2 days. Dry weight was hardly affected but phycocyanin content of both species decreased linearly to the level of UV-B radiation. Contents of protein, carotenoids and chlorophyll a were reduced only after exposure to high doses (1230 J m-2d-1) of UV-B radiation. Photosynthetic 14CO2 fixation of Anabaena cells was reduced linearly with increasing UV-B dose whereas no effect could be observed in Synechococcus. A depression of photosynthetic 15N-nitrate uptake was found after UV-B stress in both species. UV-B irradiance caused an increase of 15N-incorporation into glutamine, but no effect was noted for incorporation into alanine or aspartic acid. An increase of 15N-excess in glutamic acid linear with the UV-B dose was observed in Synechococcus, only. Patterns of 14C-labelled photosynthetic products were either less affected by UV-B radiation (Anabaena) or an enhancement of 14C-label in total amino acids was detected (Synechococcus). The amount of total free amino acids increased parallel to the level of UV-B radiation. Only, the high dose of UV-B (1405 J m-2 d-1, weighted) results in a decrease of the glutamine pool. Our results indicate an inhibition of glutamate synthase by UV-B irradiation in Anabaena, only. Results were discussed with reference to the damage of the photosynthetic apparatus. (orig.)

  8. Biomarker and carbon isotope constraints (δ13C, Δ14C) on sources and cycling of particulate organic matter discharged by large Siberian rivers draining permafrost areas

    International Nuclear Information System (INIS)

    Circumpolar permafrost soils store about half of the global soil organic carbon pool. These huge amounts of organic matter (OM) could accumulate due to low temperatures and water saturated soil conditions over the course of millennia. Currently most of this OM remains frozen and therefore does not take part in the active carbon cycle, making permafrost soils a globally important carbon sink. Over the last decades mean annual air temperatures in the Arctic increased stronger than the global mean and this trend is projected to continue. As a result the permafrost carbon pool is under climate pressure possibly creating a positive climate feedback due to the thaw-induced release of greenhouse gases to the atmosphere. Arctic warming will lead to increased annual permafrost thaw depths and Arctic river runoff likely resulting in enhanced mobilization and export of old, previously frozen soil-derived OM. Consequently, the great arctic rivers play an important role in global biogeochemical cycles by connecting the large permafrost carbon pool of their hinterlands with the arctic shelf seas and the Arctic Ocean. The first part of this thesis deals with particulate organic matter (POM) from the Lena Delta and adjacent Buor Khaya Bay. The Lena River in central Siberia is one of the major pathways translocating terrestrial OM from its southernmost reaches near Lake Baikal to the coastal zone of the Laptev Sea. The permafrost soils from the Lena catchment area store huge amounts of pre-aged OM, which is expected to be remobilized due to climate warming. To characterize the composition and vegetation sources of OM discharged by the Lena River, the lignin phenol and carbon isotopic composition (δ13C and Δ14C) in total suspended matter (TSM) from surface waters, surface sediments from the Buor Khaya Bay along with soils from the Lena Delta's first (Holocene) and third terraces (Pleistocene ice complex) were analyzed. The lignin compositions of these samples are consistent

  9. Investigation of HCCI Combustion of Diethyl Ether and Ethanol Mixtures Using Carbon 14 Tracing and Numerical Simulations

    Energy Technology Data Exchange (ETDEWEB)

    Mack, J H; Dibble, R W; Buchholz, B A; Flowers, D L

    2004-01-16

    Despite the rapid combustion typically experienced in Homogeneous Charge Compression Ignition (HCCI), components in fuel mixtures do not ignite in unison or burn equally. In our experiments and modeling of blends of diethyl ether (DEE) and ethanol (EtOH), the DEE led combustion and proceeded further toward completion, as indicated by {sup 14}C isotope tracing. A numerical model of HCCI combustion of DEE and EtOH mixtures supports the isotopic findings. Although both approaches lacked information on incompletely combusted intermediates plentiful in HCCI emissions, the numerical model and {sup 14}C tracing data agreed within the limitations of the single zone model. Despite the fact that DEE is more reactive than EtOH in HCCI engines, they are sufficiently similar that we did not observe a large elongation of energy release or significant reduction in inlet temperature required for light-off, both desired effects for the combustion event. This finding suggests that, in general, HCCI combustion of fuel blends may have preferential combustion of some of the blend components.

  10. Constraints on emissions of carbon monoxide, methane, and a suite of hydrocarbons in the Colorado Front Range using observations of 14CO2

    Directory of Open Access Journals (Sweden)

    P. P. Tans

    2013-01-01

    Full Text Available Atmospheric radiocarbon (14CO represents an important observational constraint on emissions of fossil-fuel derived carbon into the atmosphere due to the absence of 14CO in fossil fuel reservoirs. The high sensitivity and precision that accelerator mass spectrometry (AMS affords in atmospheric 14CO analysis has greatly increased the potential for using such measurements to evaluate bottom-up emissions inventories of fossil fuel CO2 (CO2ff, as well as those for other co-emitted species. Here we use observations of 14CO2 and a series of hydrocarbons and combustion tracers from discrete air samples collected between June 2009 and September 2010 at the National Oceanic and Atmospheric Administration Boulder Atmospheric Observatory (BAO; Lat: 40.050° N, Lon: 105.004° W to derive emission ratios of each species to CO2ff. From these emission ratios, we estimate emissions of these species by using the Vulcan CO2ff high resolution data product as a reference. The species considered in this analysis are carbon monoxide (CO, methane (CH4, acetylene (C2H2, benzene (C6H6, and C3–C5 alkanes. Comparisons of top-down emissions estimates are made to existing inventories of these species for Denver and adjacent counties, as well as to previous efforts to estimate emissions from atmospheric observations over the same area. We find that CO is overestimated in the 2008 National Emissions Inventory (NEI, 2008 by a factor of ~2. A close evaluation of the inventory suggests that the ratio of CO emitted per unit fuel burned from on-road gasoline vehicles is likely over-estimated by a factor of 2.5. The results also suggest that while the oil and gas sector is the largest contributor to the CH4 signal in air arriving from the north and east, it is very likely that other sources, including agricultural sources, contribute to this signal and must be accounted for when attributing these signals to oil and gas industry activity from a top-down perspective. Our results are

  11. Extensive theoretical studies on two new members of the FOX-7 family: 5-(dinitromethylene)-1,4-dinitramino-tetrazole and 1,1'-dinitro-4,4'-diamino-5,5'-bitetrazole as energetic compounds.

    Science.gov (United States)

    He, Piao; Zhang, Jian-Guo; Wang, Kun; Yin, Xin; Jin, Xin; Zhang, Tong-Lai

    2015-02-28

    Two novel compounds 5-(dinitromethylene)-1,4-dinitramino-tetrazole (DNAT) and 1,1'-dinitro-4,4'-diamino-5,5'-bitetrazole (DNABT) were suggested to be potential candidates of high energy density materials (HEDMs). The optimized geometry, NBO charges and electronic density, HOMO-LUMO, electrostatic potential on the surface of molecules, the IR spectrum and thermochemical parameters were calculated for inspecting the electronic structure properties at B3LYP/6-311++G** level of theory. Meanwhile, the solid states of DNAT and DNABT were studied using the crystal packing models by the plane-wave periodic local-density approximation density functional theory. Four stable polymorphous cells have been found including P212121, P21/c, P1̄ and Pbca, assigned to the orthorhombic, monoclinic and triclinic lattice systems. In addition, properties such as density, enthalpy of formation and detonation performance have also been predicted. As a result, the detonation velocity and pressure of two compounds are found to be very remarkable (DNAT: D = 9.17 km s(-1), P = 39.23 GPa; DNABT: D = 9.53 km s(-1), P = 40.92 GPa). Considering the tetrazole rings with energetic groups and the insensitive fragment of FOX-7, high positive heat of formation (583.50 kJ mol(-1) and 1081.39 kJ mol(-1)) and eminent performance render DNAT and DNABT to be very promising powerful energetically insensitive compounds. This work provides theoretical support for further experimental synthesis.

  12. Process for demethylating dimethylsulfonium compounds

    NARCIS (Netherlands)

    Hansen, Theo; van der Maarel, Marc

    1998-01-01

    PCT No. PCT/EP94/01640 Sec. 371 Date Nov. 14, 1995 Sec. 102(e) Date Nov. 14, 1995 PCT Filed May 16, 1994 PCT Pub. No. WO94/26918 PCT Pub. Date Nov. 24, 1994Process for preparing S-methylmercapto and mercapto compounds comprising the step of demethylating a dimethylsulfonium compound of formula I to

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

    Institute of Scientific and Technical Information of China (English)

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

    2006-01-01

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

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

    Science.gov (United States)

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

    2012-11-15

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

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

    International Nuclear Information System (INIS)

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

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

    Directory of Open Access Journals (Sweden)

    Rasoul Pourtaghavi Talemi

    2013-12-01

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

  17. The 14C as tracer in the carbon flow assimilated by the plants (maize, sugar cane, bean) and it liberation to the soil

    International Nuclear Information System (INIS)

    The flow of carbon in three different crops, maize, beans and sugar cane was studied by use of 14V. The plants were exposed to an atmosphere with a constant concentration of the tracer for 12 hours in a biosynthesis chamber. The detection of the isotope permitted the distribution and concentration of the photosynthetates in the various organs of the plants and the losses by liberation to the soil whether by root respiration or rhizodeposition to be followed. The technique of marking metabolites through photosynthesis and their detection in the various plant organs is well known and is employed despite the requirement for hight sophisticated apparatus. On the other hand the quantification of the plant-soil-microorganism interchanges presents great difficulties being dynamic processes, showing the necessity of more detailed studies. (author)

  18. First-principles calculations of the stability and hydrogen storage behavior of C14 Laves phase compound TiCrMn

    Science.gov (United States)

    Nong, Zhi-Sheng; Zhu, Jing-Chuan; Yang, Xia-Wei; Cao, Yong; Lai, Zhong-Hong; Liu, Yong; Sun, Wen

    2014-06-01

    The structural, elastic properties, electronic structure and hydrogen storage behavior of TiCrMn with a hexagonal C14 structure were investigated by the first-principles calculations within the frame work of DFT. The calculated lattice constants were consistent with the experimental values, and obtained cohesive energy and formation enthalpy showed TiCrMn is of the structural stability. These results also indicated that Mn atoms would optionally substitute on the Cr sites of TiCr2 phase to form the ternary intermetallic TiCrMn. The five independent elastic constants as well as polycrystalline elastic parameters (bulk modulus B, shear modulus G, Young's modulus E, Poisson's ratio ν and anisotropy value A) were calculated, and then the ductility and elastic anisotropy of TiCrMn were discussed in details. Furthermore, the electronic DOS and charge density distribution of TiCrMn were also calculated, which revealed the underlying mechanism of structural stability and chemical bonding. Finally, the binding energy of hydrogen in hydride TiCrMn(H3) was investigated, confirming the better hydrogen storage behavior of C14 Laves phase TiCrMn.

  19. Cost-benefit analyses for the retention of tritium, carbon 14 and krypton 85 from plants reprocessing LWR fuel elements

    International Nuclear Information System (INIS)

    ICRP's new system for the limitation of permissible doses is applied for the determination of optimum emission rates from reprocessing plants. Equivalent doses and collective doses are calculated using radioecological methods. Economy-oriented and sociological methods were used to estimate the damage to health and life expressed in monetary units (α-value equals DM 200.-/manxrem). A cost-benefit analysis was done considering retention cost, collective doses and α-value, and the results were different from those supplied by the nowadays customary retention criteria, the latter being based on the limitation of individual doses rather than collective doses. The results are surprising because for the Gorleben facility retention of krypton-85 and tritium is planned, C-14 being left out of consideration so far. (DG)

  20. Report of Carbon-14 Dates (28)%放射性碳素测定年代报告(二八)

    Institute of Scientific and Technical Information of China (English)

    中国社会科学院考古研究所考古科技实验研究中心碳十四实验室

    2002-01-01

    The present report publishes the chronological data of specimens tested by the 14C Laboratory of the Archaeological Science and Techniques Experiment and Research Center, IA, CASS, in cooperation with the Institute of Biophysics, CAS, from 1998 to 2001. These specimens, totaling 230 pieces, come from the following 11 archaeological sites: Erlitou in Yanshi County, Henan (28); Nanzhai in Yichuan County, Henan (10) ; Nianzipo in Changwu County, Shaanxi (21) ; Shang city in Yanshi, Henan (25) ; Shang city in Zhengzhou City, Henan (20+10) ; Xiaoshuangqiao in Zhengzhou City, Henan (5); Yinxu in Anyang City, Henan (43); Zhangjiapo in Chang' an City, Shaanxi (9+12); Mawangcun in Chang'an City, Shaanxi (10) ; Liulihe in Fangshan County, Beijing (25+6) ; and Jin Marquis tomb at Beizhaocun in Quwo County, Shanxi (6).

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

    OpenAIRE

    Karimi, Farhad

    2002-01-01

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

  2. Association between prenatal exposure to perfluorinated compounds and symptoms of infections at age 1-4years among 359 children in the Odense Child Cohort

    DEFF Research Database (Denmark)

    Dalsager, Louise; Christensen, Nikolas; Husby, Steffen;

    2016-01-01

    , educational level, parity and child age. RESULTS: On average, the children experienced symptoms of infection 23% of the time during one year. PFOS exposure in the high tertile compared to the low tertile was associated with a statistically significant increased proportion of days with fever (IRR: 1.65 (95% CI...... on childhood infectious disease is unclear. OBJECTIVES: To investigate the association between prenatal exposure to PFAS and symptoms of infections at age 1-4years. METHODS: The Odense Child Cohort is an on-going prospective study on children's health, where serum concentrations of perfluorooctane sulfonic......: 1.24, 2.18), P-trendfever above the median (OR: 2.35 (95% CI: 1.31, 4.11). The latter tendency was also apparent for PFOA (OR: 1.97 (95% CI: 1.07, 3.62). Further, higher concentrations of PFOS and PFOA tended to increase the number of episodes...

  3. Microstructural Evolution and Compressive Properties of Two-Phase Nb-Fe Alloys Containing the C14 Laves Phase NbFe2 Intermetallic Compound

    Science.gov (United States)

    Li, K. W.; Wang, X. B.; Wang, W. X.; Li, S. M.; Gong, D. Q.; Fu, H. Z.

    2016-02-01

    Microstructural evolution and compressive properties of two-phase Nb-Fe binary alloys based on the C14 Laves phase NbFe2 were characterized at both the hypo- and hypereutectic compositions. The experimental results indicated that the microstructures of the two alloys consisted of fully eutectics containing Fe and NbFe2 phases at the bottom of the ingots corresponding to the largest solidification rates. With the decrease of solidification rate, the microstructures developed into primary Fe (NbFe2) dendrites plus eutectics in the middle and top parts of the ingots. The microstructural evolutions along the axis of the ingots were analyzed by considering the competitive growth between the primary phase and eutectic as well as using microstructure selection models based on the maximum interface temperature criterion. Furthermore, the compressive properties of the two alloys were measured and the enhancements were explained in terms of the second Fe phase and halo toughening mechanisms.

  4. Near Surface Leakage Monitoring for the Verification and Accounting of Geologic Carbon Sequestration Using a Field Ready {sup 14}C Isotopic Analyzer

    Energy Technology Data Exchange (ETDEWEB)

    Marino, Bruno

    2014-04-14

    Results for the development of a field ready multi-isotopic analyzer for {sup 12}CO{sub 2}, {sup 13}CO{sub 2} and {sup 14}CO{sub 2} and applications for carbon capture and storage (CCS) containment performance are described. A design goal of the field platform was to provide isotopic data with a high data rate, a standardized reference baseline and acceptable precision (e.g., ~ ±50 per mil D{sup 14}CO{sub 2}) for detection and quantification of fossil-fuel CO{sub 2} CCS leakage scenarios. The instrument platform was not designed to replace high precision accelerator mass spectrometry. An additional goal was to combine project scale isotopic data and associated fluxes with unique financial instruments linking CCS containment performance to a publicly traded security providing project revenue to stakeholders. While the primary goals of the project were attained additional work is needed for the instrument platform and deployment within a full scale CCS site that was not available during the project timeframe.

  5. Studies of palaeovegetation changes in the Central Amazon by carbon isotopes (12C, 13C, 14C) of soil organic matter

    International Nuclear Information System (INIS)

    The paper presents carbon isotope data δ13C and 14C on soil organic matter collected along an ecosystem transect in southern Amazon state, north-central Amazon region, that includes three distinct vegetation communities: savannah (Campos de Humaita), a savannah-forest transition and forest (Manaus). The study sites are located along road BR 319. Botanical identification and 13C analysis of modern vegetation in the savannah and forest sites indicate that most of the vegetation is C3 plants, although a few C4 plants are present at Campos de Humaita. The 13C and 14C data for soil organic matter in the Humaita region show that significant vegetation changes have occurred in the past, probably associated with climatic changes. During the early Holocene, forest vegetation extended throughout the study region, including areas occupied today by savannah vegetation. Savannah vegetation expanded at least 2 km into the modern forest ecotone during the middle Holocene, suggesting drier conditions. The last approximately 1000 years appear to indicate a recent expansion of forest vegetation, reflecting a return to a more moist climate. The study illustrates that the transition area between forest and savannah vegetation is quite sensitive to climatic changes, and this region should be the focus of more extensive research related to past climate and vegetation dynamics in the Amazon region. (author)

  6. Application of Carbon Black G660 in the Sidewall Compound of Industrial Vehicle Tire%炭黑G660在工业车辆轮胎胎侧胶中的应用

    Institute of Scientific and Technical Information of China (English)

    孟海狮; 彭广海; 朱令

    2015-01-01

    研究炭黑G660在工业车辆轮胎胎侧胶中的应用。结果表明,与炭黑N660胶料相比,炭黑G660胶料的300%定伸应力、拉伸强度和撕裂强度相差不大,拉断伸长率较大,生热较低,耐屈挠性能较好,工艺性能满足生产要求,成本降低,成品轮胎物理性能相当。%In this study, carbon black G660 was applied in the sidewall compound of industrial vehicle tire. The results showed that, compared with carbon black N660 filled compound, the tensile modulus at 300%elongation, tensile strength and tear strength of G660 iflled compound were similar, the elongation at break was larger, heat build-up was lower, and lfex resistance was better. The processing property of the compound iflled with G660 met the production requirements and the cost was reduced. The ifnished tire with G660 iflled sidewall showed similar physical properties as that with N660 iflled sidewall.

  7. [1,2]-Wittig Rearrangement of THP Acetal Compounds: Facile Synthesis of Aromatic Tertiary Alcohols

    Directory of Open Access Journals (Sweden)

    Feng-Lei Gu

    2011-01-01

    Full Text Available Several sec-aromatic THP acetal compounds have been found to be suitable substrates for the [1,2]-Wittig rearrangement in the absence of an external electrophile, which resulted in the generation of new carbon-carbon bond and the facile synthesis of aromatic tertiary alcohols. More interestingly, an unexpected effect of chlorotrimethylsilane on this [1,2]-Wittig rearrangement of sec-aromatic THP acetal compounds was found, in which two different products involving oxidative procedure were obtained due to the competitive [1,4]-Sigmatropic rearrangement versus [1,2]-Wittig rearrangement

  8. Accuracy of a rapid 10-minute carbon-14 urea breath test for the diagnosis of Helicobacter pylori-associated peptic ulcer disease

    International Nuclear Information System (INIS)

    Urease in the human gastric mucosa is a marker for infection with Helicobacter pylori (HP), an organism which is associated with peptic ulcer disease. To detect gastric urease, we examined 184 patients (144 males, 40 females; mean age: 49.8±15.6 years) with suspected peptic ulcer disease. Fasting patients were given orally 5 μCi of carbon-14 labelled urea. For each patient only one breath sample was collected in hyamine at 10 min. The amount of 14C collected at 10 min was expressed as follows: [(DPM/mmol CO2 collected)/(DPM administered)]x100xbody weight (kg). The presence of HP colonization was determined by examination of multiple endoscopic prepyloric antral biopsy specimens subjected to culture or a rapid urease test. For the purpose of this study, HP-positive patients were defined as those with characteristic bacteria as indicated by a positive result of either the culture or the rapid urease test; HP-negative patients were defined as those with negative findings on both the culture and the rapid urease test. Of the 184 cases, 99 (53.8%) were positive for HP infection, and 85 (46.2%), negative. The sensitivity and specificity of the rapid 10 min 14C-urea breath test for the diagnosis of HP-associated peptic ulcer disease were evaluated by a receiver operating characteristic (ROC) curve with a variable cut-off value from 1.5 to 4.5. When a cut-off value of 1.5 was selected, the sensitivity was 100% and the specificity, 83.5%; when a cut-off value of 4.5 was selected, the sensitivity was 54.5% and the specificity, 97.6%. (orig.)

  9. A Model-based Interpretation of Low-frequency Changes in the Carbon Cycle during the Last 120,000 years and its Implications for the Reconstruction of Atmospheric (delta) 14-C

    Science.gov (United States)

    Koehler, Peter; Muscheler, Raimund; Fischer, Hubertus

    2006-01-01

    A main caveat in the interpretation of observed changes in atmospheric (Delta)C-l4 during the last 50,000 years is the unknown variability of the carbon cycle, which together with changes in the C-14 production rates determines the C-14 dynamics. A plausible scenario explaining glacial/interglacial dynamics seen in atmospheric CO2 and (delta)C-13 was proposed recently (Kohler et al., 2005a). A similar approach that expands its interpretation to the C-14 cycle is an important step toward a deeper understanding of (Delta)C-14 variability. This approach is based on an ocean/atmosphere/biosphere box model of the global carbon cycle (BICYCLE) to reproduce low-frequency changes in atmospheric CO2 as seen in Antarctic ice cores. The model is forced forward in time by various paleoclimatic records derived from ice and sediment cores. The simulation results of our proposed scenario match a compiled CO2 record from various ice cores during the last 120,000 years with high accuracy (r(sup 2) = 0.89). We analyze scenarios with different C-14 production rates, which are either constant or based on Be-10 measured in Greenland ice cores or the recent high-resolution geomagnetic field reconstruction GLOPIS-75 and compare them with the available (Delta)C-14 data covering the last 50,000 years. Our results suggest that during the last glacial cycle in general less than 110%0o f the increased atmospheric (Delta)C-14 is based on variations in the carbon cycle, while the largest part (5/6) of the variations has to be explained by other factors. Glacial atmospheric (Delta)C-14 larger than 700% cannot not be explained within our framework, neither through carbon cycle-based changes nor through variable C-14 production. Superimposed on these general trends might lie positive anomalies in atmospheric (Delta)C-14 of approx. 50% caused by millennial-scale variability of the northern deep water production during Heinrich events and Dansgaard/Oeschger climate fluctuations. According to our

  10. Leaf waxes, compound-specific D/H and 14C analyses in the Loess Paleosol Sequence Möhlin, Switzerland

    Science.gov (United States)

    Wüthrich, Lorenz; Bliedtner, Marcel; Kathrin Schäfer, Imke; Zech, Jana; Gaar, Dorian; Preusser, Frank; Zech, Roland

    2016-04-01

    Leaf waxes, such as long-chain n-alkanes and n-alkanoic acids, and their D/H isotopic composition, are increasingly used for paleoenvironmental and -climate reconstructions. Recent technological innovations now also allow to perform radiocarbon analyses on leaf waxes. For this study, we analyzed leaf waxes and their δD and 14C composition in the 7 m Loess Paleosol Sequence Möhlin, Switzerland. The chain length patterns in the upper part of the profile indicate n-alkane contribution from deciduous trees, while the underlying loess is dominated by inputs from grasses and herbs. Our δD record does not show depleted, glacial values compared to the Holocene, as we had expected in analogy to the Greenland ice core records. Values are most enriched at 1 m depth, i.e. well below the topsoil. Further research is needed to disentangle source effects and evapotranspirative enrichment, before the δD record can be interpreted robustly. Our radiocarbon ages for the leaf waxes are in very good agreement with independent age control based on luminescence ages, corroborating that massive loess accumulation occurred already at 35 ka. Only the uppermost 3 m were deposited during the last glacial maximum.

  11. Defect chemistry of the cage compound, Ca(12)Al(14)O(33-delta)-understanding the route from a solid electrolyte to a semiconductor and electride.

    Science.gov (United States)

    Lee, Doh-Kwon; Kogel, Lutz; Ebbinghaus, Stefan G; Valov, Ilia; Wiemhoefer, Hans-Dieter; Lerch, Martin; Janek, Juergen

    2009-05-01

    A crystallographic cage structure endows mayenite (Ca(12)Al(14)O(33) or 12CaO.7Al(2)O(3); C(12)A(7)) with remarkable properties, making it either an oxygen solid electrolyte or an inorganic electride upon reduction. In order to better understand the transport properties of C(12)A(7), we measured the equilibrium total conductivity as well as the electronic partial conductivity of single crystal mayenite as functions of activity of oxygen or water vapor at different temperatures in the range 1073 oxygen activity, enabling us to deconvolute the ionic and electronic partial conductivities. The ionic transference number evaluated therefrom clearly demonstrates how C(12)A(7) is converted from a solid electrolyte to an electride depending on the oxygen content. In addition, besides the well known degradation of ionic conductivity by water uptake, a short-term increase of conductivity upon abrupt hydration was recognized and interpreted as due to the transient increase in the concentration of oxygen interstitial along with proton in the initial stage of hydration. For the fully hydrated C(12)A(7), the conductivity relaxation curves upon switching of oxygen activity in a fixed water vapor pressure appear non-monotonic showing the extrema only in the plateau conductivity regime. A defect structure based hypothesis is proposed to explain the 2-fold re-equilibration kinetics. PMID:19370205

  12. Reaction of hydrogen with the Laves phase (C14) TiCr{sub 1.78-x}Mn{sub x} compounds

    Energy Technology Data Exchange (ETDEWEB)

    Agresti, F. [Universita di Padova, Dipartimento di Ingegneria Meccanica, Settore Materiali and CNISM, via Marzolo 9, 35131 Padova (Italy); Lo Russo, S. [Universita di Padova, Dipartimento di Fisica and CNISM, via Marzolo 8, 35131 Padova (Italy); Maddalena, A.; Principi, G. [Universita di Padova, Dipartimento di Ingegneria Meccanica, Settore Materiali and CNISM, via Marzolo 9, 35131 Padova (Italy); Mazzolai, G. [Universita di Perugia, Dipartimento di Fisica, Via A. Pascoli 5, 06100 Perugia (Italy); Universita Telematica e-Campus, Via Isimbardi 10, Novedrate (Colombia) (Italy); Coluzzi, B.; Biscarini, A. [Universita di Perugia, Dipartimento di Fisica, Via A. Pascoli 5, 06100 Perugia (Italy); Mazzolai, F.M., E-mail: fabio.mazzolai@fisica.unipg.it [Universita di Perugia, Dipartimento di Fisica, Via A. Pascoli 5, 06100 Perugia (Italy); Tuissi, A. [Istituto per l' Energia e le Interfasi, CNR-IENI, C.so Promessi Sposi, 29, Lecco (Italy)

    2009-09-15

    The lattice constants a and c of the as cast hexagonal (C14) Laves phase TiCr{sub 1.78-x}Mn{sub x} (x = 0, 0.4, 0.6 and 0.8) have been measured by X-ray diffraction at room temperature as a function of the Mn content. It has been found that a decreases with increasing x while c remains almost unchanged. Being this alloy interesting as material for solid state hydrogen storage, pressure-composition isotherms have been traced on desorption mode for the H{sub 2} gas pressure and temperature varying from 10 to 0.01 MPa and from 209 to 307 K, respectively. From the temperature dependence of the plateau pressure the molar quantities {Delta}H-bar{sub H{sub 2}} and {Delta}S-bar{sub H{sub 2}} associated with the hydride decomposition have been determined as a function of the Mn content. With increasing x, both {Delta}H-bar{sub H{sub 2}} and {Delta}S-bar{sub H{sub 2}} progressively decrease, and the desorption pressure initially decreases (for x {<=} 0.4) then slightly increases. At the same time, the pseudo-plateaus become flatter.

  13. The Path of Carbon in Photosynthesis IX. Photosynthesis, Photoreduction, and the Hydrogen-Oxygen-Carbon Dioxide Dark Reaction

    Science.gov (United States)

    Badin, E. J.; Calvin, M.

    1950-02-01

    A comparison of the rates of fixation of Carbon 14 dioxide in algae for the processes of photosynthesis, photoreduction and the hydrogen-oxygen-carbon dioxide dark reaction has been made. For the same series of experiments, rates of incorporation of tracer carbon into the separate soluble components using the radiogram method have been determined. The mechanism of carbon dioxide uptake has been shown to occur via two distinct paths. In all cases studied, essentially the same compounds appear radioactive. The distribution with time, however, differs markedly.

  14. Determining novel functions of Arabidopsis 14-3-3 proteins in central metabolic processes

    Directory of Open Access Journals (Sweden)

    Diaz Celine

    2011-11-01

    Full Text Available Abstract Background 14-3-3 proteins are considered master regulators of many signal transduction cascades in eukaryotes. In plants, 14-3-3 proteins have major roles as regulators of nitrogen and carbon metabolism, conclusions based on the studies of a few specific 14-3-3 targets. Results In this study, extensive novel roles of 14-3-3 proteins in plant metabolism were determined through combining the parallel analyses of metabolites and enzyme activities in 14-3-3 overexpression and knockout plants with studies of protein-protein interactions. Decreases in the levels of sugars and nitrogen-containing-compounds and in the activities of known 14-3-3-interacting-enzymes were observed in 14-3-3 overexpression plants. Plants overexpressing 14-3-3 proteins also contained decreased levels of malate and citrate, which are intermediate compounds of the tricarboxylic acid (TCA cycle. These modifications were related to the reduced activities of isocitrate dehydrogenase and malate dehydrogenase, which are key enzymes of TCA cycle. In addition, we demonstrated that 14-3-3 proteins interacted with one isocitrate dehydrogenase and two malate dehydrogenases. There were also changes in the levels of aromatic compounds and the activities of shikimate dehydrogenase, which participates in the biosynthesis of aromatic compounds. Conclusion Taken together, our findings indicate that 14-3-3 proteins play roles as crucial tuners of multiple primary metabolic processes including TCA cycle and the shikimate pathway.

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

    Science.gov (United States)

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

    2005-12-01

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

  16. Synthesis of carbon-13 labelled carbonaceous deposits and their evaluation for potential use as surrogates to better understand the behaviour of the carbon-14-containing deposit present in irradiated PGA graphite

    Science.gov (United States)

    Payne, L.; Walker, S.; Bond, G.; Eccles, H.; Heard, P. J.; Scott, T. B.; Williams, S. J.

    2016-03-01

    The present work has used microwave plasma chemical vapour deposition to generate suitable isotopically labelled carbonaceous deposits on the surface of Pile Grade A graphite for use as surrogates for studying the behaviour of the deposits observed on irradiated graphite extracted from UK Magnox reactors. These deposits have been shown elsewhere to contain an enhanced concentration of 14C compared to the bulk graphite. A combination of Raman spectroscopy, ion beam milling with scanning electron microscopy and secondary ion mass spectrometry were used to determine topography and internal morphology in the formed deposits. Direct comparison was made against deposits found on irradiated graphite samples trepanned from a Magnox reactor core and showed a good similarity in appearance. This work suggests that the microwave plasma chemical vapour deposition technique is of value in producing simulant carbon deposits, being of sufficiently representative morphology for use in non-radioactive surrogate studies of post-disposal behaviour of 14C-containing deposits on some irradiated Magnox reactor graphite.

  17. Extensive theoretical studies on two new members of the FOX-7 family: 5-(dinitromethylene)-1,4-dinitramino-tetrazole and 1,1'-dinitro-4,4'-diamino-5,5'-bitetrazole as energetic compounds.

    Science.gov (United States)

    He, Piao; Zhang, Jian-Guo; Wang, Kun; Yin, Xin; Jin, Xin; Zhang, Tong-Lai

    2015-02-28

    Two novel compounds 5-(dinitromethylene)-1,4-dinitramino-tetrazole (DNAT) and 1,1'-dinitro-4,4'-diamino-5,5'-bitetrazole (DNABT) were suggested to be potential candidates of high energy density materials (HEDMs). The optimized geometry, NBO charges and electronic density, HOMO-LUMO, electrostatic potential on the surface of molecules, the IR spectrum and thermochemical parameters were calculated for inspecting the electronic structure properties at B3LYP/6-311++G** level of theory. Meanwhile, the solid states of DNAT and DNABT were studied using the crystal packing models by the plane-wave periodic local-density approximation density functional theory. Four stable polymorphous cells have been found including P212121, P21/c, P1̄ and Pbca, assigned to the orthorhombic, monoclinic and triclinic lattice systems. In addition, properties such as density, enthalpy of formation and detonation performance have also been predicted. As a result, the detonation velocity and pressure of two compounds are found to be very remarkable (DNAT: D = 9.17 km s(-1), P = 39.23 GPa; DNABT: D = 9.53 km s(-1), P = 40.92 GPa). Considering the tetrazole rings with energetic groups and the insensitive fragment of FOX-7, high positive heat of formation (583.50 kJ mol(-1) and 1081.39 kJ mol(-1)) and eminent performance render DNAT and DNABT to be very promising powerful energetically insensitive compounds. This work provides theoretical support for further experimental synthesis. PMID:25631492

  18. Synthesis of 2, 4-- dichloro phenoxy acetic acid [ Carboxy- 14 C] as herbicide

    International Nuclear Information System (INIS)

    One of the important herbicide, that can be used for the practical mechanism investigations and studies of metabolism functions of different plants is 2,4 dichlorophenoxy acetic acid compound. In this article, the production method for labeling the titled compound is explained. At the first stage of this research work, barium[14C] carbonate is converted into potassium [14C] by using potassium azid at a reasonable temperature. Then, after a few synthesis reaction, the compound 2,4 dichlorophenoxy methyl iodide is produced via 2,4 dichlorophenoxy as a starting material. At the next stage, the real material as a herbicide: 2,4 dichlorophenoxy acetic acid [carboxy- 14C] is prepared and produced, by the coupling reaction between 2,4 dichlorophenoxy methyl iodide and potassium [14C] cyanide, and then the resulting nitrile has been hydrolyzed

  19. Traceability of animal byproducts in quail (Coturnix coturnix japonica tissues using carbon (13C/12C and nitrogen (15N/14N stable isotopes

    Directory of Open Access Journals (Sweden)

    C Móri

    2007-12-01

    Full Text Available Consistent information on meat products consumed by the public is essential. The technique of stable isotopes is a powerful tool to recover consumers' confidence, as it allows the detection of animal byproduct residues in poultry meat, particularly in quail meat. This study aimed at checking the presence of poultry byproduct mixtures in quail diets by applying the technique of carbon (13C/12C and nitrogen (15N/14N stable isotopes in quail breast muscle, keel, and tibia. Sixty four one-day-old male quails were obtained from a commercial farm. Birds were housed in an experimental house from one to 42 days of age, and were randomly distributed into 8 experimental treatments, and fed diets containing poultry offal meal (POM, bovine meat and bone meal (MBM or poultry feather meal (PFM, or their mixtures. Four birds per treatment were slaughtered at 42 days of age, and breast (Pectoralis major, keel, and tibia were collected for analyses. The inclusion of animal byproducts in quail diets was detected by 13C e 15N analyses in the tissues of the birds; however, it was not possible to specify which byproducts were used. It was concluded that quail meat can be certified by the technique of stable isotopes.

  20. Carbon-rich presolar grains from massive stars. Subsolar 12C/13C and 14N/15N ratios and the mystery of 15N

    CERN Document Server

    Pignatari, M; Hoppe, P; Jordan, C J; Gibson, B K; Trappitsch, R; Herwig, F; Fryer, C; Hirschi, R; Timmes, F X

    2015-01-01

    Carbon-rich grains with isotopic anomalies compared to the Sun are found in primitive meteorites. They were made by stars, and carry the original stellar nucleosynthesis signature. Silicon carbide grains of Type X and C, and low-density graphites condensed in the ejecta of core-collapse supernovae. We present a new set of models for the explosive He shell and compare them with the grains showing 12C/13C and 14N/15N ratios lower than solar. In the stellar progenitor H was ingested into the He shell and not fully destroyed before the explosion. Different explosion energies and H concentrations are considered. If the SN shock hits the He-shell region with some H still present, the models can reproduce the C and N isotopic signatures in C-rich grains. Hot-CNO cycle isotopic signatures are obtained, including a large production of 13C and 15N. The short-lived radionuclides 22Na and 26Al are increased by orders of magnitude. The production of radiogenic 22Ne from the decay of 22Na in the He shell might solve the pu...