WorldWideScience

Sample records for carbon 14

  1. Carbon 14

    International Nuclear Information System (INIS)

    2002-03-01

    Carbon 14 is one of the most abundant radionuclides of natural and artificial origin in the environment. The aim of this conference day organized by the French society of radioprotection (SFRP) was to take stock of our knowledge about this radionuclide (origins, production, measurement, management, effects on health..): state-of-the-art of 14 C metrology; dating use of 14 C; 14 C management and monitoring of the Hague site environment; Electricite de France (EdF) and 14 C; radiological and sanitary impact of 14 C contamination at the Ganagobie site (Haute-Provence, France); metabolism and biological effects of 14 C; 14 C behaviour in the marine environment near Cogema-La Hague plant; distribution of 14 C activities in waters, mud and sediments of the Loire river estuary; dynamical modeling of transfers in the aquatic and terrestrial environment of 14 C released by nuclear power plants in normal operation: human dose calculation using the Calvados model and application to the Loire river; 14 C distribution in continents; modeling of 14 C transfers in the terrestrial environment from atmospheric sources. (J.S.)

  2. Carbon-14 waste management

    International Nuclear Information System (INIS)

    Bush, R.P.; Smith, G.M.; White, I.F

    1984-01-01

    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 14 N 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. Carbon-14 waste management

    International Nuclear Information System (INIS)

    Bush, R.P.

    1984-01-01

    As part of their research programme on Radioactive Waste Management, the Commission of the European Communities has provided financial support for a detailed study of wastes containing 14 C and the options for their management. The main results of this study are outlined. Carbon-14 is formed by neutron activation reactions in core materials and is therefore present in a variety of waste streams both at reactors and at reprocessing plants. Data on the production and release of 14 C from various reactor systems are presented. A possible management strategy for 14 C might be reduction of 14 N impurity levels in core materials, but only reductions of about a factor of five in arisings could be achieved in this way. The key problem in 14 C management is its retention in off-gas streams, particularly in the dissolver off-gas stream at reprocessing plants. In this stream the nuclide is present as carbon dioxide and is extensively isotopically diluted by the carbon dioxide content of the air. Processes for trapping 14 C from these off-gases must be integrated with the other processes in the overall off-gas treatment system, and should provide for conversion to a stable solid compound of carbon, suitable for subsequent immobilization and disposal. Three trapping processes that convert carbon dioxide into insoluble carbonates can be identified: the double alkali (NaOH/Ca(OH) 2 ) process, the direct calcium hydroxide slurry process, and the barium ocathydrate gas/solid process. Calcium or barium carbonates, produced in the above processes, could probably be incorporated into satisfactory immobilized waste forms. However, the stability of such waste forms to prolonged irradiation and to leaching remains to be investigated. (author)

  4. Carbon-14 Graphitization Chemistry

    Science.gov (United States)

    Miller, James; Collon, Philippe; Laverne, Jay

    2014-09-01

    Accelerator Mass Spectrometry (AMS) is a process that allows for the analysis of mass of certain materials. It is a powerful process because it results in the ability to separate rare isotopes with very low abundances from a large background, which was previously impossible. Another advantage of AMS is that it only requires very small amounts of material for measurements. An important application of this process is radiocarbon dating because the rare 14C isotopes can be separated from the stable 14N background that is 10 to 13 orders of magnitude larger, and only small amounts of the old and fragile organic samples are necessary for measurement. Our group focuses on this radiocarbon dating through AMS. When performing AMS, the sample needs to be loaded into a cathode at the back of an ion source in order to produce a beam from the material to be analyzed. For carbon samples, the material must first be converted into graphite in order to be loaded into the cathode. My role in the group is to convert the organic substances into graphite. In order to graphitize the samples, a sample is first combusted to form carbon dioxide gas and then purified and reduced into the graphite form. After a couple weeks of research and with the help of various Physics professors, I developed a plan and began to construct the setup necessary to perform the graphitization. Once the apparatus is fully completed, the carbon samples will be graphitized and loaded into the AMS machine for analysis.

  5. Compilation of carbon-14 data

    International Nuclear Information System (INIS)

    Paasch, R.A.

    1985-01-01

    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)

    Fortin, Ph.

    2000-01-01

    This document gives a first introduction to 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 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 14 C dates; the preparation of samples; the benzene synthesis; the current applications of the method. (J.S.)

  8. Carbon-14 in sludge

    International Nuclear Information System (INIS)

    Fowler, J.R.; Coleman, C.J.

    1983-01-01

    The level of C-14 in high-level waste is needed to establish the amount of C-14 that will be released to the environment either as off-gas from the Defense Waste Processing Facility (DWPF) or as a component of saltstone. Available experimental data confirmed a low level of C-14 in soluble waste, but no data was available for sludge. Based on the processes used in each area, Purex LAW sludge in F-area and HM HAW sludge in H-area will contain the bulk of any sludge produced by the cladding. Accordingly, samples from Tank 8F containing Purex LAW and Tank 15H containing HM HAW were obtained and analyzed for C-14. These two waste types constitute approximately 70% of the total sludge inventory now stored in the waste tanks. Results from analyses of these two sludge types show: the total C-14 inventory in sludge now stored in the waste tanks is 6.8 Ci; C-14 releases to the atmosphere from the DWPF will average approximately 0.6 Ci annually at the projected sludge processing rate in the DWPF. 4 references, 2 tables

  9. Carbon-14 in tree rings

    International Nuclear Information System (INIS)

    Cain, W.F.; Suess, H.E.

    1976-01-01

    In order to investigate how reliably the carbon 14 content of tree rings reflects that of atmospheric carbon dioxide, two types of determinations were carried out: (1) carbon 14 determinations in annual rings from the beginning of this century until 1974 and (2) carbon 14 determinations in synchronous wood from the North American bristlecone pine and from European oak trees, dendrochronologically dated to have grown in the third and fourth century B.C. The first series of measurements showed that bomb-produced radiocarbon was incorporated in wood at a time when it was converted from sapwood to heartwood, whenever radiocarbon from bomb testing was present in the atmosphere. The second series showed that wood more than 2000 years old and grown on two different continents at different altitudes had, within the limits of experimental error, the same radiocarbon content. This work and other experimental evidence, obtained in part by other laboratories, show that tree rings reflect the average radiocarbon content of global atmospheric carbon dioxide accurately within several parts per mil. In rare cases, deviations of up to 10 parts per thousand may be possible. This means that a typical single radiocarbon date for wood or charcoal possesses an intrinsic uncertainty (viz., an estimated ''one-sigma error'' in addition to all the other errors) of the order of +-50 years. This intrinsic uncertainty is independent of the absolute age of the sample. More accurate dates can, in principle, be obtained by the so-called method of ''wiggle matching.''

  10. Selection of a carbon-14 fixation form

    International Nuclear Information System (INIS)

    Scheele, R.D.; Burger, L.L.

    1982-09-01

    This report summarizes work on the selection of a disposal form for carbon-14 produced during the production of nuclear power. Carbon compounds were screened on the basis of solubility, thermal stability, resistance to oxidation, cost and availability, compatibility with the selected disposal matrix, leach resistance when incorporated in concrete, and compatibility with capture technologies. Carbonates are the products of the various technologies presently considered for carbon-14 capture. The alkaline earth carbonates exhibit the greatest thermal stabilities, lowest solubilities, lowest raw material cost, and greatest raw material availabilities. When reactions with cement and its impurities are considered, calcium and strontium carbonates are the only alkaline earth carbonates resistant to hydrolysis and reaction with sulfate. Leaching tests of barium, calcium, lead, potassium, and strontium carbonates in concrete showed calcium carbonate concrete to be slightly superior to the other alkaline earth carbonates, and greatly superior to a soluble carbonate, potassium carbonate, and lead carbonate. None of the additives to the concrete reduced the carbonate leaching. Acidic CO 2 -containing waters were found to greatly increase carbonate leaching from concrete. Sea water was found to leach less carbon from carbonate concretes than either distilled water or Columbia River water, which showed nearly equivalent leaching. Based on our work, calcium, barium, and strontium carbonates in concrete are the most suitable waste forms for carbon-14, with calcium carbonate concrete slightly superior to the others. If the waste form is to be exposed to natural waters, sea water will have the lowest leach rate. 6 figures, 7 tables

  11. Adsorption of carbon-14 on mortar

    International Nuclear Information System (INIS)

    Matsumoto, Junko; Banba, Tsunetaka; Muraoka, Susumu

    1995-01-01

    The sorption experiments of carbon-14 on the mortar grain (grain size: 0.50--1.0 mm) focused on the chemical form of the carbon-14 were carried out by the batch method. Three kinds of carbon-14 chemical form were used for the experiments: sodium carbonate (Na 2 14 CO 3 ) as the inorganic radiocarbon, and sodium acetate (CH 3 14 COONa) and acetaldehyde ( 14 CH 3 14 CHO) as the organic radiocarbons. 0.30 gram samples of mortar were soaked in the solution with carbon-14 at 15 C for periods of up to 160 days. At the end of each run, carbon-14 concentrations in the supernatants were determined before and after centrifugation (3,500 rpm., 1 hr). In the mortar-sodium carbonate system, the retention process of carbon-14 related to reaction on the surface of the mortar was speculated as follows. First, 3CaO-SiO 2 and 2CaO-SiO 2 of the mortar components contact with water and produce Ca(OH) 2 . Ca(OH) 2 produces Ca 2+ and OH - in the solution. Then, calcite forms from Ca 2+ and CO 3 2- in the solution. Thus, the sorption ratio of carbon-14 onto mortar will be high until mortar has been completely carbonated because Ca 2+ is rich in the mortar and the solubility of calcite is low. In the mortar-organic carbon system, the soluble organic carbon-14 is hardly sorbed on the surface of the mortar. Therefore, the cementitious materials may not inhibit the release of organic radiocarbons from the low-level radioactive wastes, contrary to the case of inorganic radiocarbon

  12. Carbon-14 as an hydrology tool

    International Nuclear Information System (INIS)

    Garcia y G, E.; Albarran B, R.

    1977-01-01

    Carbon-14 and tritium results from the action of cosmic radiation and of nuclear tests also. In general carbon-14 resulting from nuclear arms tests is of no interest from the hydrological point-of view, as tritium is a more efficient marker of juvenile waters through having a much shorter disintegration period. Radioactive carbon oxidizes and forms carbon dioxide which mixes with atmospheric carbon dioxide and enters the global carbon cycle. Use of carbon-14 in the dating of subterranean waters is based on the fact that the carbon dioxide found in the soil zone is of biologic origin arising from the respiration and decomposition of plant roots. Therefore it contains carbon-14 taken from the atmosphere by the plants. This carbon dioxide of biogenic origin is dissolved in infiltrating water and is borne along towards the water bearing strata. Its carbon-14 content decrease through radioactive loss and the fractional remainder of the original contents indicates the time which has passed since it left the supply zone in the soil, that is, the time passed since it filtrated the water. (author)

  13. 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.

  14. 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.)

  15. Carbon and carbon-14 in lunar soil 14163

    International Nuclear Information System (INIS)

    Fireman, E.L.; Stoenner, R.W.

    1981-01-01

    Carbon is removed from the surface of lunar soil 14163 size fractions by combustions at 500 and 1000 0 C in an oxygen stream and the carbon contents and the carbon-14 activities are measured. The carbon contents are inversely correlated with grain size. A measured carbon content of 198 ppM for bulk 14163, obtained by combining the size fraction results, is modified to 109 +- 12 ppM by a carbon contamination correction. This value is in accord with a previous determination, 110 ppM, for bulk 14163. The small ( 53 μ) grains, 11.2 +- 2.0 dpm/kg. The combusted carbon and carbon-14 are attributed mainly to solar-wind implantation. Melt extractions of carbon-14 from the combusted soil samples gave essentially identical activities, 21.0 +- 1.5 and 19.2 +- 2.0 dpm/kg for the small and large grains, and are attributed to cosmic-ray spallation-produced carbon-14

  16. Carbon 14 and tritium radioactivity of alcohols

    International Nuclear Information System (INIS)

    Guerain, J.; Tourliere, S.

    1975-01-01

    The method of measuring carbon 14 radioactivity of alcohols has been perfected in order to establish the correct determination of synthetic alcohol added to fermentation alcohol. The specific carbon and tritium activity of alcohol of different origins have been determined for 1973 and 1974. The Suess effect and nuclear fall-out are observed [fr

  17. Carbon-14 measurements in aquifers with methane

    International Nuclear Information System (INIS)

    Barker, J.F.; Fritz, P.; Brown, R.M.

    1979-01-01

    A survey of various groundwater systems indicates that methane is a common trace constituent and occasionally a major carbon species in groundwaters. Thermocatalytic methane had delta 13 Csub(CH 4 )>-45 per mille and microbially produced or biogenic methane had delta 13 Csub(CH 4 ) 13 C values for the inorganic carbon. Thermocatalytic methane had no apparent effect on the inorganic carbon. Because methanogenesis seriously affects the carbon isotope geochemistry of groundwaters, the correction of raw 14 C ages of affected groundwaters must consider these effects. Conceptual models are developed which adjust the 14 C activity of the groundwater for the effects of methanogenesis and for the dilution of carbon present during infiltration by simple dissolution of rock carbonate. These preliminary models are applied to groundwaters from the Alliston sand aquifer where methanogenesis has affected most samples. In this system, methanogenic bacteria using organic matter present in the aquifer matrix as substrate have added inorganic carbon to the groundwater which has initiated further carbonate rock dissolution. These processes have diluted the inorganic carbon 14 C activity. The adjusted groundwater ages can be explained in terms of the complex hydrogeology of this aquifer, but also indicate that these conceptual models must be more rigorously tested to evaluate their appropriateness. (author)

  18. Synthesis of carbon-14 labeled vigabatrin. [Antieplileptic

    Energy Technology Data Exchange (ETDEWEB)

    Schuster, A.J.; Wagner, E.R. (Marion Merrell Dow Inc, Indianapolis, IN (United States))

    1993-01-01

    Carbon-14 labeled vigabatrin was synthesized in 5 steps from 5-hydroxymethyl-2-pyrrolidone tosylate and NaCN-[[sup 14]C]. A key step involved reduction of the resulting nitrile in the presence of excess dimethylamine to give the dimethylamino-ethyl 2-pyrrolidone derivative in one step. This afforded an overall radiochemical yield of 22% and radiochemical purity greater than 98%. (Author).

  19. Synthesis of carbon-14 labelled ethyl chloride

    International Nuclear Information System (INIS)

    Kanski, R.

    1976-01-01

    A new efficient method of synthesis of ethyl chloride (1,2- 14 C), based on the Ba 14 CO 3 and dry hydrogen chloride as starting materials has been developed and described. Addition of the hydrogen chloride to ethylene (1,2- 14 C), obtained from Ba 14 CO 3 , has been carried out in the presence of the AlCl 3 as catalyst. The outlined method leads to ethyl chloride (1,2- 14 C) of high specific activity. The radiochemical yield of the reaction based on the activity of barium carbonate used was 72%. (author)

  20. Carbon-14 production in nuclear reactors

    International Nuclear Information System (INIS)

    Davis, W. Jr.

    1977-01-01

    The radioactive nuclide 14 C is formed in all nuclear reactors due to absorption of neutrons by carbon, nitrogen, or oxygen. These may be present as components of the fuel, moderator, or structural hardware, or they may be present as impurities. Most of the 14 C formed in the fuels or in the graphite of HTGRs will be converted to a gaseous form at the fuel reprocessing plant, primarily as carbon dioxide; this will be released to the environment unless special equipment is installed to collect it and convert it to a solid for essentially permanent storage. If the 14 C is released as carbon dioxide or in any other chemical form, it will enter the biosphere, be inhaled or ingested as food by nearly all living organisms including man, and will thus contribute to the radiation burden of these organisms. Detailed estimates are presented of the amounts of 14 C formed in LWRs, HTGR, and LMFBR with emphasis on those pathways that are likely to lead to the release of this nuclide, either at the reactor site or at the fuel reprocessing plant. 83 references

  1. Concentration of carbon-14 in plants

    International Nuclear Information System (INIS)

    1978-01-01

    The carbon-14 survey program initiated 1960 to gather data on current levels of carbon-14 in environments. Plants essential oil and fermented alcohol were selected as sample materials. The carbon contained in these materials is fixed from atmospheric carbon dioxide by anabolism, so they well reflect the variation of carbon-14 in biosphere. Thymol; Thymol was obtained from the essential oil of Orthodon Japonicium Benth which was cultivated and harvested every year in the experimental field of NIRS and Chiba University. The methylation was carried out to eliminate the strong quenching action of the phenolic group of thymol. Eighteen grams of thymol methyl ether was used as liquid scintillator by adding 0.4% PPO and 0.01% POPOP. Menthol; Menthol was obtained from Mentha arvensis L which was cultivated in the east part of Hokkaido and prepared by Kitami Factory of Federation of Agricultural Cooperative Society of Hokkaido. The chemical conversion of menthol to p-cymene was carried out and used as liquid scintillator as same as above sample. Lemongrass oil; Lemongrass oil was obtained from Cymbopogon citratus Stapf which was cultivated in Izu Experimental Station of Medicinal Plants, National Institute of Hygienic Science located Minami-Izu, Shizuoka Pref. The p-cymene derived from Lemongrass oil was used as liquid scintillator. Alcohol; All sample of fermented alcohol were obtained from the Alcohol Factories of Ministry of Trade and Industry. Raw materials of alcohol were sweet potatos cultivated in several prefectures in Japan ''high test'' molasses and blackstrap molasses imported from several countries of Asia, South America and South Africa, crude alcohol imported from U.S.A., Argentina and Brazil. Mixed solvent of 10 ml sample alcohol and 10 ml toluene or p-xylene containing 0.8% PPO and 0.1% dimethyl POPOP was used as liquid scintillator. (author)

  2. 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)

    Dolan, M.M.

    1987-01-01

    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

  3. 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 dates...

  4. Global impact of carbon-14 from nuclear power reactors

    International Nuclear Information System (INIS)

    Moghissi, A.A.; Carter, M.W.

    1977-01-01

    Carbon-14 is produced by nuclear power reactors, predominently as a result of the interaction of a neutron and nitrogen-14 both in the fuel and in the coolant. Several other reactions also contribute to the production of carbon-14. Present operational procedures, in general, for reactors and fuel reprocessing plants result in the release of carbon-14 into the environment. Combustion of fossil fuels and certain industrial operations contribute to the supply of CO 2 in the atmosphere and this contribution is essentially free of carbon-14. Future carbon-14 burdens by assuming a thorough mixing of all CO 2 in the atmosphere is predicted. Available data on electric power generation, fossil fuel combustion and certain other information are used to calculate the projected specific activity of carbon-14 by the year 2000 and the twenty-first century. According to these calculations, the global population dose from carbon-14 can be substantial. Also, carbon-14 in the vicinity of nuclear power reactors is considered. Because of the chemistry of carbon-14, it is shown that local problems may be more significant around BWR's as compared to PWR's. Based on environmental considerations of carbon-14, its increasing production and discharge into the atmosphere, and available control technology, it is recommended that nitrogen use and its presence be minimized in pertinent reactor components and operations

  5. Carbon 14 in the aquatic food chain

    International Nuclear Information System (INIS)

    Mueller, H.; Fischer, E.

    1983-01-01

    In the links of the food chain consisting of water, water plants, and fish from 6 several aquatic ecosystems, the specific C-14 activity of the carbon was determined from 1979 to 1981 and compared with values of the terrestrial food chain. The mean values obtained from the specific acitivities of the links were between 203 and 321 mBq/g C (5.5 and 8.7 pCi/g C). Four of the six mean values differ from the values for the terrestrial food chain of 260 to 240 mBg/g C (7.0 to 6.5 pCi/g C) investigated for 1979 to 1980. The specific-acitivity model is valid for the aquatic food chain only if atmosphere and man are not included as chain links. (orig.) [de

  6. An improved synthesis of carbon-14 labelled carboxylic acids from carbon-14 labelled amino acids

    International Nuclear Information System (INIS)

    Ramamurthy, T.V.; Ravi, S.; Viswanathan, K.V.

    1988-01-01

    Various carbon-14 labelled amino acids including the aromatic ones viz., tyrosine, phenylalanine and tryptophan are converted to the corresponding carboxylic acids in high yield (70-90%) on a micromolar scale synthesis by reaction with hydroxyl-amine-O-sulphonic acid and in a short reaction time. The improvement in yield has been achieved by using aqeuous alcohol as solvent in lieu of water alone as the medium of reaction. (author)

  7. 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.)

  8. Measurement of carbon-14 in hydrological samples

    International Nuclear Information System (INIS)

    Hussain, S.D.

    1991-11-01

    Thermal neutrons produced by cosmic rays or nuclear weapon tests interact with atmospheric nitrogen resulting in the formation of radiocarbon which, after oxidation into carbon dioxide, follows the natural carbon cycle. The partial pressure of carbon dioxide in the soil is several times that in the atmosphere due to plant root respiration and decay of organic matter. Water absorbs biogenic carbon dioxide while percolating through the unsaturated zone. The carbon content of groundwater is mainly in the form of bicarbonate ions. The extraction of carbon from water sample as barium carbonate is carried out in the field. Benzene is synthesised from the carbonate sample. The activity of radiocarbon in the synthesised benzene is determined by using a liquid scintillation analyzer. Details of sampling procedure, benzene synthesis, counter calibration and treatment of sample data have been given. 7 figs. (author)

  9. Dual labelling of Lobuprofen with tritium and carbon-14

    International Nuclear Information System (INIS)

    Santamaria, J.; Rivera, P.; Esteban, M.; Martin, J.L.; Carretero, J.M.

    1988-01-01

    Dual labelling of Lobuprofen with tritium and carbon-14 was performed. The synthesis between 2-(4-isobutylphenyl)propionic acid (Ibuprofen), randomly labelled with tritium, and 2-[4-(3-chlorophenyl)-1-piperazinyl]ethanol (Cl-Alkanol) labelled with carbon-14 in the piperazine ring was achieved. Prior to this synthesis, the [ 14 C]Cl-Alkanol was obtained using 2-amino-[2- 14 C]ethanol as a precursor. (author)

  10. The EC CAST project (carbon-14 source term)

    International Nuclear Information System (INIS)

    Williams, S. J.

    2015-01-01

    Carbon-14 is a key radionuclide in the assessment of the safety of underground geological disposal facilities for radioactive wastes. It is possible for carbon-14 to be released from waste packages in a variety of chemical forms, both organic and inorganic, and as dissolved or gaseous species The EC CAST (CArbon-14 Source Term) project aims to develop understanding of the generation and release of carbon-14 from radioactive waste materials under conditions relevant to packaging and disposal. It focuses on the release of carbon-14 from irradiated metals (steels and zirconium alloys), from irradiated graphite and from spent ion-exchange resins. The CAST consortium brings together 33 partners. CAST commenced in October 2013 and this paper describes progress to March 2015. The main activities during this period were reviews of the current status of knowledge, the identification and acquisition of suitable samples and the design of experiments and analytical procedures. (authors)

  11. The synthesis of carbon-14 labeled pravastatin

    International Nuclear Information System (INIS)

    Wallace, M.A.; Dean, D.C.; Ellsworth, R.L.; Melillo, D.G.; Marks, T.; White, R.F.

    1993-01-01

    An asymmetric route to [ 14 C]β-hydroxycompactin 1 bearing the (S)-2-methyl-[1- 14 C]butanoate side chain has been developed. Methylation of [N-[1- 14 C]butyryl]-4-(S)-phenylmethyl-2-oxazolidinone 4 afforded a 95:5 mixture of diastereomeric [N-(S,R)-2-methyl-[1- 14 C]butyryl]-4-(S)-phenylmethyl-2-oxazolidi nones 5,6 which were separated by preparative HPLC. Oxidative cleavage of 5 afforded optically pure (S)-2-methyl-[1- 14 C]butanoic acid. Acylation of alcohol 9 with optically pure (S)-2-methyl-[1- 14 C] butyryl chloride afforded ester 10. Removal of the silyl ether produced diastereomerically pure compactin 11. Hydroxylation was carried out by biotransformation with Mucor hiemelus to afford diastereomerically pure [[1- 14 C]butanoate]β-hydroxycompactin, [ 14 C]Pravastatin 1. (Author)

  12. Preparation of carbon-14-labelled gallic acid

    International Nuclear Information System (INIS)

    Kozak, I.; Prochazka, M.

    1977-01-01

    Gallic acid labelled with 14 C was prepared for the needs of biological studies. A lithium derivative of trimethoxybenzene was treated with 14 CO 2 and then demethylated to yeld [carboxyl- 14 C]gallic acid. The preparation scheme and the individual steps of the synthesis are described in detail

  13. Distribution of carbon-14 assimilated by wheat awns

    International Nuclear Information System (INIS)

    Olugbemi, L.B.

    1978-01-01

    The pattern of distribution of carbon assimilated by awns was investigated in two lines of Triticum aestivum. Single awns on basal florets of spikelets in the central part of the ear were dosed with 14 C0 2 . Five days after dosing, 99% of the carbon-14 recovered was in the spikelet bearing the awn. Of the carbon-14 exported from the treated awn 57% went to the grain of the first floret, 1% to the second, 28% to the third and 7% to the fourth. (author)

  14. Gases and carbon in metals. Pt. 14

    International Nuclear Information System (INIS)

    Jehn, H.; Speck, H.; Hehn, W.; Fromm, E.; Hoerz, G.

    1981-01-01

    This issue is part of a series of data on 'Gases and Carbon in Metals' which supplements the data compilation in the book 'Gase und Kohlenstoff in Metallen' (Gases and Carbon in Metals), edited by E. Fromm and E. Gebhardt, Springer-Verlag, Berlin 1976. The present survey includes results from papers published after the copy deadline and recommends critically selected data. Furthermore, it comprises a bibliography of relevant literature. For each element, firstly data on binary systems are presented, starting with hydrogen and followed by carbon, nitrogen, oxygen, and rare gases. Within one metal-metalloid system the data are listed under topics such as solubility, solubility limit, dissociation pressure of compounds, vapour pressure of volatile oxides, thermodynamic data, diffusion, transport parameters (effective valence, heat of transport), permeation of gases through metals, gas absorption and gas desorption kinetics, compound formation kinetics, precipitation kinetics, and property changes. Following the data on binary systems, the data of ternary systems are presented, beginning with systems which contain one metal and two gases or one gas and carbon and continuing with systems with two metals and one gas or carbon. (orig./GE)

  15. Quantifying Carbon-14 for Biology Using Cavity Ring-Down Spectroscopy

    OpenAIRE

    McCartt, A. Daniel; Ognibene, Ted J.; Bench, Graham; Turteltaub, Kenneth W.

    2016-01-01

    A cavity ring-down spectroscopy (CRDS) instrument was developed using mature, robust hardware for the measurement of carbon-14 in biological studies. The system was characterized using carbon-14 elevated glucose samples and returned a linear response up to 387 times contemporary carbon-14 concentrations. Carbon-14 free and contemporary carbon-14 samples with varying carbon-13 concentrations were used to assess the method detection limit of approximately one-third contemporary carbon-14 levels...

  16. Isotopic labelling with carbon-14 and tritium

    International Nuclear Information System (INIS)

    Evans, E.A.

    1980-01-01

    In this paper general methods of isotopic labelling with 14 C and with 3 H are briefly reviewed with special attention to examples of compounds likely to be of wide interest in biological research. (author)

  17. Chemoenzymatic synthesis of carbon-14 labelled antioxidants

    International Nuclear Information System (INIS)

    Deigner, H.P.; Freyberg, C.; Heck, R.

    1993-01-01

    The syntheses of [ 14 C] labelled antioxidants are described. We developed an efficient synthetic methodology to prepare a series of labelled amides with antioxidant activity, starting from [ 14 C] KCN and alkyl or aryl halides. By a combination of nucleophilic displacement of halides by [ 14 C] cyanide, mediated by ultrasound and subsequent mild and selective enzymatic hydrolysis of the resulting nitriles, labelled carboxylic acids were obtained. Labelled amines were prepared by reduction of the respective nitriles. Availability of [ 14 C] KCN, efficient introduction of the label by ultrasound mediated reaction and selective and mild hydrolysis by commercially available nitrilase (Rhodococcus sp.), makes possible a wide range of applications of this methodology in the synthesis of functionalized labelled compounds. (Author)

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

    International Nuclear Information System (INIS)

    Garcia Pineda, M.D.; Suarez Contreras, C.; Rodrigo Gonzalez, M.E.

    1978-01-01

    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 2 produced from 14 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

  19. Carbon-14 in reactor plant water

    International Nuclear Information System (INIS)

    Knowles, G.K.

    1979-01-01

    The method for the analysis of 14 C in reactor plant water and various waste streams previously used at the Idaho National Engineering Laboratory has been shown to be ineffective for samples which contain organic compounds. The previous method consisted of acidification and refluxing of the sample, precipitation of the liberated CO 2 , and subsequent analysis by the liquid scintillation method. The method was simple but it did not convert all compounds containing 14 C in the sample to CO 2 . The new method, while it is based on the previous method, has been improved by employing a strong oxidant, potassium persulfate and silver nitrate, for more complete oxidation of the organics to CO 2 . The new method yields 14 C values that have typically been one to two orders of magnitude higher than the values obtained using the former method. This indicates that most of the 14 C present in the current reactor water samples being analyzed is associated with trace amounts of organics

  20. Dynamics of carbon 14 in soils: a review

    International Nuclear Information System (INIS)

    Tamponnet, C.

    2004-01-01

    In terrestrial ecosystems, soil is the main interface between atmosphere, hydrosphere, lithosphere and biosphere. Its interactions with carbon cycle are primordial. Information about carbon 14 dynamics in soils is quite dispersed and an up-to-date status is therefore presented in this paper. Carbon 14 dynamics in soils are governed by physical processes (soil structure, soil aggregation, soil erosion) chemical processes (sequestration by soil components either mineral or organic), and soil biological processes (soil microbes, soil fauna, soil biochemistry). The relative importance of such processes varied remarkably among the various biomes (tropical forest, temperate forest, boreal forest, tropical savannah, temperate pastures, deserts, tundra, marshlands, agro ecosystems) encountered in the terrestrial eco-sphere. Moreover, application for a simplified modelling of carbon 14 dynamics in soils is proposed. (author)

  1. Carbon-14 labeling of phytoplankton carbon and chlorophyll a carbon: determination of specific growth rates

    International Nuclear Information System (INIS)

    Welschmeyer, N.A.; Lorenzen, C.J.

    1984-01-01

    The pattern of photosynthetic 14 C labeling over time is described for phytoplankton. The carbon-specific growth rate (d -1 ) is defined explicitly by changes in the specific activity (dpm μg -1 C) of the algae. For Skeletonema costatum, growing in axenic batch culture, the specific activities of both total cellular carbon and chlorophyll carbon increase at equal rates and the change in specific activity with time follows the predicted pattern. The specific activity of 14 C-labeled chlorophyll a was used to estimate phytoplankton growth rates and C:Chl ratios of field samples in Dabob Bay (Puget Sound), Washington. Growth rates decreased with depth and C:Chl ratios were higher for samples incubated under high light intensity. In several instances the C:Chl ratio increased from the beginning to the end of the incubation; this trend was most conspicuous near surface light intensities and for days of high total incident radiation. On these occasions, Chl a was actively 14 C labeled, yet little (or even negative) change was noted in the concentration of Chl a. These results suggest that some process (or processes) of chlorophyll degradation must be active at the same time that chlorophyll is being synthesized

  2. Determination of carbon-14 environmental samples by mixing 14CO2 with a liquid scintillator

    International Nuclear Information System (INIS)

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

    1990-01-01

    A method for the determination of Carbon-14 ( 14 CO 2 ) 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-CO 2 ) to the liquid scintillator. The results obtained to apply this method and the benzene synthesis, usual in our laboratory, are discused and compared. The method of collection of atmospheric samples is also described. (Author)

  3. Determination of Carbon-14 in environmental samples by mixing 14CO2 with a liquid scintillator

    International Nuclear Information System (INIS)

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

    1990-01-01

    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

  4. Syntheses of carbon-14 and sulfur-35 labeled 2-(Morpholinothio)-benzothiazoles and carbon-14 labeled 2-(Cyclohexylaminothio)-benzothiazoles

    Energy Technology Data Exchange (ETDEWEB)

    Tanaka, A.; Fukuoka, M.; Adachi, T.; Yamaha, T.

    1986-04-01

    Some vulcanizing accelerators, mercaptobenzothiazole derivatives labeled with carbon-14 or sulfur-35 were prepared. 2-(Morpholinothio)benzothiazole labeled with carbon-14 or sulfur-35 of the sulfhydryl group at position 2 was synthesized by oxidative condensation with sodium hypochlorite from a mixture of morpholine and 2-mercaptobenzothiazole-2-/sup 14/C or 2-mercaptobenzothiazole-2-/sup 35/S. The same method was applicable to the synthesis of 2-(morpholino-U-/sup 14/C-thio) -benzothiazole using morpholine-U-/sup 14/C as starting material. 2-(Cyclohexylaminothio)benzothiazole-2-/sup 14/C was prepared, by oxidation with a mixture of iodine and potassium iodide, from cyclohexylamine and 2-mercapto-benzothiazole-2-/sup 14/C, which was synthesized from carbon-/sup 14/C disulfide and 2-mercaptoaniline in the presence of trace sodium sulfide in dimethylformamide. 2-(Cyclohexyl-U-/sup 14/C-aminothio)benzothiazole was also obtained from cylcohexyl-amine-U-/sup 14/C and 2-mercaptobenzothiazole.

  5. Synthesis of carbon-13 and carbon-14 labeled paldimycin tri-sodium salt

    International Nuclear Information System (INIS)

    Hsi, R.S.P.; Witz, D.F.; Visser, J.; Stolle, W.T.; Ditto, C.L.

    1989-01-01

    Carbon-14 labeled paldimycin trisodium salt was prepared by addition of N-acetyl-L-cysteine to [ 14 C]paulomycin, the radioactive antibiotic produced by fermentation of Streptomyces paulus in the presence of L-methionine labeled with carbon-14 in the S-methyl group. Carbon-13 nuclear magnetic resonance (NMR) spectra of paulomycin produced when the fermentation was carried out in the presence of L-[S-methyl- 13 C]methionine showed that the isotope incorporation had occurred specifically at the methoxy group of ring C, i.e., the 2-deoxy sugar portion of paulomycin. With sustained slow feed of labeled precursors during the optimum antibiotic production period, carbon-14 isotope yields of up to 17.5% with specific activity of up to 11.4 μCi per milligram of paulomycin, and carbon-13 isotope yields of up to 24% with 17-fold isotope enrichment over natural abundance, were achieved. (author)

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

    International Nuclear Information System (INIS)

    Lysakova, Katerina; Neumann, Jan; Vonkova, Katerina

    2012-09-01

    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 17 O and nitrogen 14 N 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 (CH 4 and CO 2 ) 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

  7. Carbon-14 measurements and characterization of dissolved organic carbon in ground water

    International Nuclear Information System (INIS)

    Murphy, E.M.

    1987-01-01

    Carbon-14 was measured in the dissolved organic carbon (DOC) in ground water and compared with 14 C analyses of dissolved inorganic carbon (DIC). Two field sites were used for this study; the Stripa mine in central Sweden, and the Milk River Aquifer in southern Alberta, Canada. The Stripa mine consists of a Precambrian granite dominated by fracture flow, while the Milk River Aquifer is a Cretaceous sandstone aquifer characterized by porous flow. At both field sites, 14 C analyses of the DOC provide additional information on the ground-water age. Carbon-14 was measured on both the hydrophobic and hydrophilic organic fractions of the DOC. The organic compounds in the hydrophobic and hydrophilic fractions were also characterized. The DOC may originate from kerogen in the aquifer matrix, from soil organic matter in the recharge zone, of from a combination of these two sources. Carbon-14 analyses, along with characterization of the organics, were used to determine this origin. Carbon-14 analyses of the hydrophobic fraction in the Milk River Aquifer suggest a soil origin, while 14 C analyses of the hydrophilic fraction suggest an origin within the Cretaceous sediments (kerogen) or from the shale in contact with the aquifer

  8. The 14 mu m band of carbon stars

    NARCIS (Netherlands)

    Yamamura, [No Value; de Jong, T; Waters, LBFM; Cami, J; Justtanont, K; LeBertre, T; Lebre, A; Waelkens, C

    1999-01-01

    We have studied the absorption bands around 14 mum in the spectra of 11 carbon stars with mass-loss rates ranging from 10(-8) to 10(-4) M-circle dot yr(-1), based on data obtained with the Short Wavelength Spectrometer (SWS) on board the Infrared Space Observatory (ISO). All stars clearly show a

  9. The metabolism and dosimetry of carbon-14 labelled compounds

    International Nuclear Information System (INIS)

    Crawley, F.E.H.

    1977-01-01

    The number of compounds labelled at high specific activity with carbon-14 has greatly increased over the last few years. There are limited biological data available to enable an assessment of the internal radiation dose and to identify the critical tissues after an intake of such compounds. The ICRP consider two Model Systems for deriving dose. Both Models assume a total elimination of the carbon-14 in the breath and only bone or whole body as critical tissues and are not representative of the majority of the compounds now available. A research programme has been established to study the rate of excretion and tissue distribution of selected carbon-14 labelled compounds in the rat after intravenous injection, pulmonary and gastric intubation and skin absorption. These metabolic data have been used to calculate the committed dose equivalent and maximum permissible annual intake (MPAI) for various tissues in man on the assumption that the experimental data obtained in the rat are true for man. To date potassium 14 C-cyanide and 14 C-methanol have been studied. The values for the MPAI's derived from the doses to individual tissues are more restrictive than values calculated from the whole body doses. The MPAI calculated from excretion data in terms of whole body dose is 31 mCi for 14 C-cyanide and 25 mCi for 14 C-methanol. However, the critical tissue for 14 C-cyanide is the stomach with an MPAI of 1.5 mCi based on a dose of 10.7 rem mCi -1 . This was an order of magnitude greater than the dose to any other region of the GI tract and 5 times that to the testis. The critical organs for 14 C-methanol are the testis (MPAI 2.5 mCi) for males and the ovaries (MPAI 6.2 mCi) for females

  10. Carbon-14 dating of groundwater under Christchurch, 1976 samples

    International Nuclear Information System (INIS)

    Stewart, M.K.; Brenninkmeijer, C.A.M.; Brown, L.J.

    1986-06-01

    Four samples of groundwater from deep aquifers under Christchurch have been analysed for carbon-14, tritium, oxygen-18 and chemical contents. Interpretation of the carbon-14 results requires two steps, (1) correction of the measured 14 C values for input of dead ( 14 C-free) carbon underground (indicating that the measured values of 80 PMC* should be increased to about 120 PMC), and (2) determination of water residence times for given flow models of the groundwater system. Interpretation of tritium results involves step 2 only. Three models are considered, of which the third is considered most appropriate to Christchurch. In this model, the 14 C and T results indicate that a small proportion of young water (post-1954) mixes with a larger proportion of older water (probably at least several hundred years). The oxygen-18 content indicates that recharge is mainly from the Waimakariri River and possibly from rainfall and streams near the foothills of the Canterbury Plains. Other aspect of the groundwater flow under Christchurch are discussed

  11. Preparation of pyridostigmine bromide labeled with carbon-14 and tritium

    Energy Technology Data Exchange (ETDEWEB)

    Kepler, J.A.; Twine, C.E.; Austin, R.D. (Research Triangle Inst., Research Triangle Park, NC (United States))

    1992-08-01

    [2-[sup 14]C]Pyridostigmine bromide was prepared in 17.6% radiochemical yield with specific activity of 18 mCi/mmol. The reaction sequence involved preparation of 2-furan[[sup 14]C]carboxylic acid by carbonation of 2-lithiofuran, followed by conversion to 2-amino[[sup 14]C]methylfuran by lithium aluminium hydride reduction of its carboxamide. Oxidative rearrangement of 2-amino[[sup 14]C]methylfuran gave 3-hydroxy[2-[sup 14]C]pyridine which was converted to [2-[sup 14]C]pyridostigmine bromide by reaction with dimethylcarbamyl chloride and quarternization with bromomethane. Pyridostigmine bromide labeled in the methyl group of the carbamate function was prepared in 73% yield with specific activity of 37.6 mCi/mmol by reaction of bis-3-pyridyl carbonate with [[sup 14]C]dimethylamine followed by quarternization with bromomethane. [6-[sup 3]H]-Pyridostigmine bromide with specific activity of 22.5 mCi/mmol was prepared by catalytic halogen-tritium replacement of 2,6-dibromo-3-dimethylcarbamyloxypyridine followed by quarternization with bromomethane and back-exchanging the labile 2-tritium. (author).

  12. Preparation of pyridostigmine bromide labeled with carbon-14 and tritium

    International Nuclear Information System (INIS)

    Kepler, J.A.; Twine, C.E.; Austin, R.D.

    1992-01-01

    [2- 14 C]Pyridostigmine bromide was prepared in 17.6% radiochemical yield with specific activity of 18 mCi/mmol. The reaction sequence involved preparation of 2-furan[ 14 C]carboxylic acid by carbonation of 2-lithiofuran, followed by conversion to 2-amino[ 14 C]methylfuran by lithium aluminium hydride reduction of its carboxamide. Oxidative rearrangement of 2-amino[ 14 C]methylfuran gave 3-hydroxy[2- 14 C]pyridine which was converted to [2- 14 C]pyridostigmine bromide by reaction with dimethylcarbamyl chloride and quarternization with bromomethane. Pyridostigmine bromide labeled in the methyl group of the carbamate function was prepared in 73% yield with specific activity of 37.6 mCi/mmol by reaction of bis-3-pyridyl carbonate with [ 14 C]dimethylamine followed by quarternization with bromomethane. [6- 3 H]-Pyridostigmine bromide with specific activity of 22.5 mCi/mmol was prepared by catalytic halogen-tritium replacement of 2,6-dibromo-3-dimethylcarbamyloxypyridine followed by quarternization with bromomethane and back-exchanging the labile 2-tritium. (author)

  13. Carbon-14 geochemistry at the Savannah River Site

    International Nuclear Information System (INIS)

    Roberts, Kimberly A.; Kaplan, Daniel I.

    2013-01-01

    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 14 C did not sorbed to sediments or cementitious materials, i.e., that C-14 K 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 14 C as CO 2 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 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 14 C, as dissolved carbonate, sorbs to and desorbs from SRS sediments and cementitious materials. Laboratory studies measuring the sorption of 14 C, added as a carbonate, showed unequivocally that 14 C-carbonate K 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 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 d model, may be a more accurate description of the 14 C-carbonate sorption process. A second study demonstrated that the 14 C-carbonate sorbed very strongly onto the

  14. 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.)

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

    International Nuclear Information System (INIS)

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

    1980-01-01

    Adult female and stage V Calanus pacificus were fed 14 C-labeled phytoplankton in the laboratory in the form of monospecific cultures and natural populations. A carbon budget was constructed by following the 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

  16. Accelerator mass analyses of meteorites - carbon-14 terrestrial ages

    International Nuclear Information System (INIS)

    Miura, Y.; Rucklidge, J.; Beukens, R.; Fireman, E.

    1988-01-01

    Carbon-14 terrestrial ages of ten Antarctic meteorites have been measured by the IsoTrace accelerator mass spectrometry (AMS). The 14 C terrestrial age of 1 gram sample was determined from 14 C concentrations collected at melt and re-melt temperatures, compared with the 14 C concentration of the known Bruderheim chondrite. Yamato-790448 (LL3) chondrite was found to be the oldest terrestrial age of 3x10 4 years in the nine Yamato chondrites, whereas Yamato-791630 (L4) chondrite is considered to be the youngest chondrites less than thousand years. Allan Hills chondrite of ALH-77231 (L6) shows older terrestrial age than the nine Yamato chondrites. New accelerator data of the terrestrial age show higher accuracy with smaller sample than the previous counting method. (author)

  17. Synthesis of carbon-14 analogue of 1,5 diaryl-5-[14C]-1,2,3-triazoles

    International Nuclear Information System (INIS)

    Matloubi, Hojatollah; Shafiee, Abbas; Saemian, Nader; Shirvani, Gholamhossein; Daha, Fariba Johari

    2004-01-01

    Two 1,2,3-triazole anticonvulsants, 1-(4-methylsulfone-phenyl)-5-(4-methyl-phenyl)-1,2,3-triazole and 1-(4-methylsulfone-phenyl)-5-phenyl-1,2,3-triazole, both labeled with carbon-14 in the 5-position were prepared from para-tolunitrile-[cyano- 14 C] and benzonitrile-[cyano- 14 C], respectively

  18. The management of carbon-14 in Canadian nuclear facilities

    International Nuclear Information System (INIS)

    1995-07-01

    In Canada, Derived Emission Limits (DELs) for the release of radionuclides from nuclear facilities are set to ensure that the dose to a member of a critical group from one year's release does not exceed the limit on annual dose to a member of the public set by the Atomic Energy Control Regulations. The Advisory Committee on Radiological Protection (ACRP) has expressed concerns as to whether this procedure provides adequate protection to members of the public, including future generations, for certain radionuclides such as a carbon-14 ( 14 C), which can accumulate in the environment and which can be dispersed, through environmental processes, beyond the local region where the critical group is assumed to live. The ACRP subsequently established a Working Group to review the production, release, environmental levels, and waste management of 14 C arising in CANDU power reactors. The ACRP recommendations resulting from this review can be summarized as · Given the current levels of emissions from CANDU nuclear power stations resulting from the use of a carbon dioxide annulus gas and the limitations in the calculation and use of collective dose, the ACRP sees no need for and additional collective dose limit to be applied to these sources. · The AECB should require licensees of power reactors and waste management sites to provide an annual inventory of 14 C held within reactor buildings and waste management sites; to provide information on the stability of the ion exchange resins and their continuing ability to retain the 14 C; to demonstrate on an ongoing basis that releases of 14 C are maintained at a small fraction of the emission limits; and to report annually the critical group and local collective doses arising from releases of 14 C. 61 refs., 25 tabs., 4 figs

  19. Carbon-14 dating of tree rings for tritium measurement

    International Nuclear Information System (INIS)

    Yamada, Y.; Yasuike, K.; Kiriyama, N.; Komura, K.; Ueno, K.

    1998-01-01

    The carbon-14 concentration in tree-ring cellulose of an 80-year-old pine tree which has been used for tritium measurement was measured during the 1941-1987 period. This was done to determine the formation year of each tree ring in order to study the pathway of tritium uptake into the tree rings. In the 1941 to 1953 period, the δ 14 C value remained slightly lower than 0 per mille. It began to increase from 1954 to a small broad peak of 250 per mille between 1959 and 1961, followed by rapid increase to the highest value of approximately 800 per mille in 1964. Since 1964, it had been diminishing year by year to reach a level of 190 per mille in 1987. The two peak years coincided with those in the known carbon-14 patterns in tree rings. However, there existed a difference in the amplitude of the δ 14 C values during the period of 1963-1967. (author)

  20. Monitoring and removal of gaseous carbon-14 species

    International Nuclear Information System (INIS)

    Kabat, M.J.

    1979-01-01

    A simple and efficient method was developed for the monitoring of low level carbon-14 in nuclear power station areas and gaseous effluent. Gaseous carbon compounds (hydrocarbons and CO) are catalytically oxidized to CO 2 , which is then absorbed on solid Ca(OH) 2 at elevated temperatures. The 14 C collected is quantitatively liberated by thermal decomposition of CaCO 3 as CO 2 , which is either measured directly by flow-through detectors or absorbed in alkali hydroxide followed by liquid scintillation counting. The method can also be used for the removal of gaseous 14 C. The Ca 14 CO 3 can be immobilized in concrete for long term disposal. Ca(OH) 2 is an inexpensive absorber. It is selective for CO 2 and has high capacity and efficiency for its absorption and retention. A theoretical evaluation of thee optium conditions for CO 2 absorption and liberation is discussed and experimental investigations are described. There is good agreement between theoretical predictions and experimental findings

  1. Carbon-14 discharges from the nuclear fuel cycle: Pt. 1

    International Nuclear Information System (INIS)

    McCartney, M.; Baxter, M.S.; Scott, E.M.

    1988-01-01

    The radiological impact of 14 C produced by the nuclear fuel cycle is assessed using an advanced 25-box model of the carbon cycle coupled with a range of feasible energy-use scenarios. In particular, this study estimates both the short- and long-term dose implications to the global population. In the former context, it is predicted that the atmospheric 14 C specific activity in the year 2050 will be 234 Bq kg -1 (carbon), corresponding to delivery of an individual effective dose equivalent rate of 15 μSv year -1 . The contribution of reactor-derived 14 C to the individual dose rate increases steadily throughout this period, reaching 1.8 μSv year -1 in 2050, well within ICRP limits. In the longer term, however, the collective effective dose equivalent commitment is conservatively estimated at 141 man Sv TBq -1 , corresponding to 480 man Sv (GW(e) year) -1 . These figures indicate that 14 C could generate one of the largest contributions to the total dose to man from nuclear power production. (author)

  2. 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)

  3. Investigations on the biokinetics of carbon 14 in algae cultures

    International Nuclear Information System (INIS)

    Leister, W.

    1981-01-01

    The uptake of 14 C by Scenedesmus quadricauda is quantitatively investigated by simulation models of radio ecological relevance. Due to the complexing of the procedures in the natural ecosystem, it was only possible to consider idealized conditions. The batch culture ressembles the conditons of still waters or relatively still waters without notable water exchange. The effect of the 14 C enrichment, as well as the drastic carbon reduction in the substrate as a result of algae growth, was avoided in the modified batch culture under conditions of simultaneous substrate diffusion by means of a permeation system. The 14 C and 12 C uptake of the cells thus took place solely under the conditions of constant concentration in the culture medium. The consequences for flowing water resulting from a nuclear power plant accident are to be simulated for the extent of the 14 C uptake by green algae using the continuous culture model with dynamic 14 C exposure. The continuous infusion of 14 C in the continuous culture corresponds to the possible cases where 14 C escapes into a flowing water at a constant rate over a long period of time, whether this may be via chronical release from a nuclear power plant or by 'fallout' resulting from nuclear arms testing. The results shown lead to the conclusion that the emission of 14 C to the environment, which according to prognoses will be considerably higher after the year 2000, presents a serious radioactivity potential which man and environment will have to live with should these developments continue and the prognoses come true. (orig./MG) [de

  4. Carbon 14 distribution in irradiated BWR fuel cladding and released carbon 14 after aqueous immersion of 6.5 years

    Energy Technology Data Exchange (ETDEWEB)

    Sakuragi, T. [Radioactive Waste Management Funding and Research Center, Tsukishima 1-15-7, Chuo City, Tokyo, 104-0052 (Japan); Yamashita, Y.; Akagi, M.; Takahashi, R. [TOSHIBA Corporation, Ukishima Cho 4-1, Kawasaki Ward, Kawasaki, 210-0862 (Japan)

    2016-07-01

    Spent fuel cladding which is highly activated and strongly contaminated is expected to be disposed of in an underground repository. A typical activation product in the activated metal waste is carbon 14 ({sup 14}C), which is mainly generated by the {sup 14}N(n,p){sup 14}C reaction and produces a significant exposure dose due to the large inventory, long half-life (5730 years), rapid release rate, and the speciation and consequent migration parameters. In the preliminary Japanese safety case, the release of radionuclides from the metal matrix is regarded as the corrosion-related congruent release, and the cladding oxide layer is regarded as a source of instant release fraction (IRF). In the present work, specific activity of {sup 14}C was measured using an irradiated BWR fuel cladding (Zircaloy-2, average rod burnup of 41.6 GWd/tU) which has an external oxide film having a thickness of 25.3 μm. The {sup 14}C specific activity of the base metal was 1.49*10{sup 4} Bq/g, which in the corresponding burnup is comparable to values in the existing literature, which were obtained from various irradiated claddings. Although the specific activity in oxide was 2.8 times the base metal activity due to the additive generation by the {sup 17}O(n,α){sup 14}C reaction, the {sup 14}C abundance in oxide was less than 10% of total inventory. A static leaching test using the cladding tube was carried out in an air-tight vessel filled with a deoxygenated dilute NaOH solution (pH of 12.5) at room temperature. After 6.5 years, {sup 14}C was found in each leachate fraction of gas phase and dissolved organics and inorganics, the total of which was less than 0.01% of the {sup 14}C inventory of the immersed cladding tube. A simple calculation based on the congruent release with Zircaloy corrosion has suggested that the 96.7% of released {sup 14}C was from the external oxide layer and 3.3% was from the base Zircaloy metal. However, both the {sup 14}C abundance and the low leaching rate

  5. Production of carbon-14 and preparation of some key precursors for labeling organic molecules

    International Nuclear Information System (INIS)

    Moriya, T.; Motoishi, S.

    1992-01-01

    Production of carbon-14 on 50 GBq scale has been performed by neutron irradiation of aluminium nitride target in the JMTR. This nuclide is separated in carbon dioxide form by combustion of the irradiated target at 1100degC with oxygen. The [ 14 C] carbon dioxide liberated thus is trapped in caustic solution and finally recovered as [ 14 C] barium carbonate. Some precursors useful for incorporating carbon-14 into a given organic molecule have been prepared. Precursors such as [1- 14 C] sodium acetate, [ 14 C] methanol and [ 14 C] potassium cyanide are prepared by rather conventional methods involving carbonation of methyl magnesium iodine, reduction of carbon dioxide with lithium aluminium hydride and reduction of carbonate with metallic potassium in the presence of ammonium salt, respectively. A catalytic polymerization of acetylene is used to prepare benzene. (author)

  6. Carbon-14 labelling of biomolecules induced by 14CO ionized gas

    International Nuclear Information System (INIS)

    Lier, J.E. van; Sanche, L.

    1979-01-01

    Ionized 14 CO gas provides a rapid method for producing 14 C-labelled biomolecules. The apparatus consists of a high vacuum system in which a small amount of 14 CO is ionized by electron impact. The resulting species drift towards a target where they interact with the molecule of interest to produce 14 C-labelled compounds. Since the reaction time is only 2 minutes, the method is particularly promising for producing tracer biomolecules with short-lived 11 C at high specific activities. The applicability of the method to various classes of compounds of biological importance, including steroids, alkaloids, prostaglandins, nucleosides, amino acids and proteins has been studied. All compounds treated gave rise to 14 C addition and degradation products. Furthermore, for some compounds, chromatographic analysis in multiple systems followed by derivatization and crystallization to constant specific activity, indicated that carbon exchange may occur to produce the labelled, but otherwise unaltered substrate in yields of the order of 10-100 mCi/mol. More conclusive proof of radiochemical identity must await production of larger quantities of material and rigorous purification including at least two different chromatographic techniques. (author)

  7. Synthesis of carbon-14 analogue of 1,5 diaryl-5-[{sup 14}C]-1,2,3-triazoles

    Energy Technology Data Exchange (ETDEWEB)

    Matloubi, Hojatollah E-mail: hmatloubi@aeoi.org.ir; Shafiee, Abbas; Saemian, Nader; Shirvani, Gholamhossein; Daha, Fariba Johari

    2004-05-01

    Two 1,2,3-triazole anticonvulsants, 1-(4-methylsulfone-phenyl)-5-(4-methyl-phenyl)-1,2,3-triazole and 1-(4-methylsulfone-phenyl)-5-phenyl-1,2,3-triazole, both labeled with carbon-14 in the 5-position were prepared from para-tolunitrile-[cyano-{sup 14}C] and benzonitrile-[cyano-{sup 14}C], respectively.

  8. Tests of intestinal absorption using carbon-14-labeled isotopes

    International Nuclear Information System (INIS)

    Fromm, H.; Sarva, R.P.

    1983-01-01

    Beta radiation-emitting isotopes are being used increasingly in diagnostic gastroenterology for the study of absorption. The major reason for the popularity of radioisotopes is that their use is convenient for patient and physician alike. They often obviate naso- or orointestinal intubation and the collection, storage, and analysis of stool. The radioactivity used for the studies of digestive and absorptive processes is small and is not hazardous. In spite of the safety of the radiolabeled compounds, their use is restricted in children and pregnant women. Therefore, for most tests, promising alternative methods that make use of the stable isotope of carbon, /sup 13/C, instead of the radioactive /sup 14/C have been developed. The analysis of stable isotopes requires more sophisticated technology than that of radioactive compounds, however. Only a few centers presently are equipped and staffed to analyze stable isotopes on a routine basis. In contrast, the analysis of radioactive isotopes has become a routine procedure in almost ever major laboratory. The last decade has brought the development of several radioactive absorption tests. The clinically most useful tests relate to the study of bile acid, fat, lactose, and xylose absorption. All of these tests utilize the excretion rate of /sup 14/CO/sub 2/ in breath after ingestion of a /sup 14/C-labeled compound as a measure of the rate of its absorption or malabsorption

  9. Dating of archaeological objects using Carbon-14 facilities

    International Nuclear Information System (INIS)

    Kamisah Hj Alias; Noraishah Othman; Nasasni Nasrol

    2004-01-01

    Dating is the key to organising all archaeological evidence. Furthermore, the development of dating methods, whether traditional or scientific, illustrates the ingenuity and lateral thinking that make archaeological problem-solving such a fascinating exercise. The development of MINT radiocarbon dating procedures is reviewed. Basic principles and counting techniques are discussed. A sample is converted by chemical methods into a suitable form, such as carbon dioxide followed by the acetylene gas, and the benzene end-product is placed inside a proportional counter to measure the radioactivity of 14 C. Not until some years ago did absolute dates by radiocarbon dating become a reality for prehistoric archaeology in Malaysia where thermoluminescence and fission-track dating had begun to provide a locally applicable dating method some decades earlier. Applications of radiocarbon dating procedures in the fields of archaeology are also discussed. (Author)

  10. Improved quality control of carbon-14 labelled compounds

    International Nuclear Information System (INIS)

    Leonhardt, J.W.; Fuchs, P.; Standtke, K.

    1997-01-01

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

  11. 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.

  12. Study of the biogenesis of flavones and cinnamic acids by using molecules labelled with carbon 14

    International Nuclear Information System (INIS)

    Chabannes, Bernard

    1970-01-01

    This research thesis reports the study of flavones, flavonoid compounds and cinnamic acids which are very common as natural pigments in plant species. The author first reports the study of the synthesis of shikimic acid labelled with carbon 14 (biological methods of preparation, synthesis), and then the synthesis of prunin labelled with carbon 14. The next part reports the study of the transformation of prunin labelled with carbon 14 into cosmosiine in flowers with white cosmos. The author finally compares the introduction of cinnamic acid and of shikimic acid (both labelled with carbon 14) into the sinapic acid of red cabbage leaves

  13. Use of carbon-14 in soil organic matter studies

    International Nuclear Information System (INIS)

    Vimal, O.P.; Kamath, M.B.

    1974-01-01

    Despite a great deal of research work on various aspects of soil organic matter, there are many gaps in the knowledge of the process of humus formation. These limitations arise mainly from the complex and heterogenous nature of soil humus substances, analytical problems in separating the fresh and decomposable materials from the old stabilized true humus substances and the lack of a clear understanding of the chemical structure of the humic acid molecule. During recent years, the use of carbon-14 has helped to trace within soil, transformation of a number of metabolites upto the point where they turn into humus. These studies have changed the concepts of the formation and stability of soil humus substances, their colloidal chemical properties and the uptake of organomolecules by plant roots. The present paper presents a synoptic view of the use of radiocarbon in studying the kinetics of humification, nature of precursors in humic acid formation, turnover of soil organic matter and the direct effects of humus substances on plant growth. (author)

  14. Preparation of 14C-labelled poly(l-menthyl isopropenyl carbonates)

    International Nuclear Information System (INIS)

    Comes, R.A.; Grubbs, H.J.

    1981-01-01

    The synthesis of 14 C-labelled poly(l-menthyl isopropenyl carbonate) is described. Experimental conditions are included for incorporation of 14 C into each of the carbon atoms in the molecule. High pressure liquid chromatography conditions are given for separation and purification of the labelled intermediates. (author)

  15. Hydrogen Transfer from Hantzsch 1,4-Dihydropyridines to Carbon-Carbon Double Bonds under Microwave Irradiation

    OpenAIRE

    Jean Jacques Vanden Eynde; Didier Barbry; Guy Cordonnier; Séverine Torchy

    2002-01-01

    1,4-Dihydropyridines (DHPs) have been used in the reduction of carbon-carbon double bonds under microwave irradiation without solvent. The efficiency of the reactions is dramatically dependent on the steric effects in the DHPs and on the electronic effects in the olefins.

  16. Environmental release of carbon-14 gas from a hypothetical nuclear waste repository

    International Nuclear Information System (INIS)

    Lehto, M.A.; Merrell, G.B.

    1994-01-01

    Radioisotopes may form gases in a spent nuclear fuel waste package due to elevated temperatures or degradation of the fuel rods. Radioactive carbon-14, as gaseous carbon dioxide, is one of the gaseous radioisotopes of concern at an underground disposal facility for spent nuclear fuel and high-level radioactive waste. Carbon-14 dioxide may accumulate inside an intact waste container. Upon breach of the container, a potentially large pulse of carbon-14 dioxide gas may be released to the surrounding environment, followed by a lower, long-term continuous release. If the waste were disposed of in an unsaturated geologic environment, the carbon-14 gas would begin to move through the unsaturated zone to the accessible environment. This study investigates the transport of radioactive carbon-14 gas in geologic porous media using a one-dimensional analytical solution. Spent nuclear fuel emplaced in a deep geologic repository located at a generic unsaturated tuff site is analyzed. The source term for the carbon-14 gas and geologic parameters was obtained from previously published materials. The one-dimensional analytical solution includes diffusion, advection, radionuclide retardation, and radioactive decay terms. Two hypothetical sites are analyzed. One is dominated by advective transport, and the other is dominated by diffusive transport. The dominant transport mechanism at an actual site depends on the site characteristics. Results from the simulations include carbon-14 dioxide travel times to the accessible environment and the total release to the environment over a 10,000-year period. The results are compared to regulatory criteria

  17. An efficient synthesis of carbon-14 labelled vigabatrin

    International Nuclear Information System (INIS)

    Gill, H.S.

    1995-01-01

    Vigabatrin-[6- 14 C] ((R,S)-4-amino-5-hexenoic-[6- 14 C] acid) was synthesized by employing Wittig condensation of 1-(1-butenyl) -2-oxo-5-pyrrolidinecarboxaldehyde with methyl-[ 14 C]-triphenyl-phosphonium iodide as the key step. The synthetic sequence involved 3 steps and produced the title compound in 70% overall yield with a radiochemical purity of 100%. (author)

  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. Modelling accidental releases of carbon 14 in the environment: application as an excel spreadsheet

    International Nuclear Information System (INIS)

    Le Dizes, S.; Tamponnet, C.

    2004-01-01

    An application as an Excel spreadsheet of the simplified modelling approach of carbon 14 transfer in the environment developed by Tamponnet (2002) is presented. Based on the use of growth models of biological systems (plants, animals, etc.), the one-pool model (organic carbon) that was developed estimates the concentration of carbon 14 within the different compartments of the food chain and in fine the dose to man by ingestion in the case of a chronic or accidental release of carbon 14 in a river or the atmosphere. Data and knowledge have been implemented on Excel using the object-oriented programming language VisualBasic (Microsoft Visual Basic 6.0). The structure of the conceptual model and the Excel sheet are first briefly exposed. A numerical application of the model under a scenario of an accidental release of carbon 14 in the atmosphere is then presented. Simulation results and perspectives are discussed. (author)

  20. The metabolism and dosimetry of carbon-14 labelled diethylenetriaminepentaacetic acid (DTPA)

    International Nuclear Information System (INIS)

    Crawley, F.E.H.; Haines, J.W.

    1978-01-01

    Male rats were given carbon-14 labelled Ca-DTPA either by intravenous injection or by pulmonary intubation. The elimination of the carbon-14 by excretion in urine, faeces and breath was followed, Chromatographic examination of the urine showed that no metabolic degradation of the 14 C-DTPA had occurred. The distribution of activity between lung, kidneys, bone, muscle and GI tract was also followed. The data obtained have been used to assess the radiation dose to man from an intake of 14 C-DTPA on the assumption that the behaviour of 14 C-DTPA in man is the same as in the rat. The results are discussed. (U K.)

  1. The preparation of glucosa uniformly labelled with carbon-14

    International Nuclear Information System (INIS)

    Garcia Pineda, D.; Suarez, C.; Rodrigo Gonzalez, E.

    1978-01-01

    The plant, (Zea mais, L) and culture conditions for an optimun production of glucose has been chosen. To achieve the labelling of glucose, photosynthesis and carboxilation are carried on under an artificial atmosphere of 1 4CO 2 produced from 1 4C-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 radiactivity is determined in each of its carbon atoms. (author)

  2. Metabolism and risks from tritium and carbon-14 in the developing organism

    International Nuclear Information System (INIS)

    Gerber, G.B.; Kirchmann, R.; Hoek, J. van den

    1987-01-01

    In this review the risks are considered from tritium and carbon-14 to the developing organs of mammals. It mainly deals with H-3 but the conclusions are largely valid also for C-14. The metabolism and average tissue of THO as well as of organically bound tritium are discussed. Dosimetry of radiosensitive structures is also considered. 14 refs.; 2 figs.; 1 table

  3. An efficient synthesis of carbon-14 labelled vigabatrin

    Energy Technology Data Exchange (ETDEWEB)

    Gill, H.S. [Marion Merrell Dow Research Inst., Cincinnati, OH (United States)

    1995-12-31

    Vigabatrin-[6-{sup 14}C] ((R,S)-4-amino-5-hexenoic-[6-{sup 14}C] acid) was synthesized by employing Wittig condensation of 1-(1-butenyl) -2-oxo-5-pyrrolidinecarboxaldehyde with methyl-[{sup 14}C]-triphenyl-phosphonium iodide as the key step. The synthetic sequence involved 3 steps and produced the title compound in 70% overall yield with a radiochemical purity of 100%. (author).

  4. Radiocarbon 14C differentiation of sparkling and carbonated wines

    International Nuclear Information System (INIS)

    Martin, G.E.; Krueger, H.W.; Burggraff, J.M.

    1985-01-01

    Specific 14 C-activities, percent of modern 14 C-activity, and calculated percent of fermentation CO 2 are presented for CO 2 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 CO 2 to approximately 40 samples represented as sparkling wines was indicated by low 14 C-activities of CO 2 in these wines. Data for 14 C-activity were also presented for the ethanol distilled from sparkling wines for the years 1977-1980. In all cases, the 14 C-activity of ethanol was appropriate to the year of vintage

  5. Synthesis of bisaramil labelled with carbon-14 and deuterium

    International Nuclear Information System (INIS)

    Szammer, J.; Simon-Trompler, E.; Mlinko, S.

    1994-01-01

    [6,8- 14 C 2 ]-Bisaramil: 3-methyl-7-ethyl-9α-(4-chlorobenzoyloxy)-3,7-diazabicyclo/3. 3.1./nonane-[6,8- 14 C 2 ] monohydrochloride and [7-N-D 5 -ethyl]-Bisaramil: 3-methyl-7-[D 5 -ethyl]-9α-(4-chlorobenzoyloxy)-3,7-diazabicy clo/3.3.1./nonane monohydrochloride were synthesized in four steps from 14 CO 2 (6% overall yield) and in six steps from [D 6 ]-ethanol (4% overall yield), respectively. (Author)

  6. Synthesis of pyrimidinic nucleotides and nucleosides labelled with carbon 14, through tri-methylsilylated and lithiated derivatives

    International Nuclear Information System (INIS)

    Godbillon, Jacques

    1972-01-01

    After a presentation of the trimethysilylation, lithiation, and methylation processes, this research thesis reports the synthesis of methyl carbon 14 - 5 - uridine, of ethyl carbon 14 - 5 - desoxy - 2' - uridine, and of thymidine monophosphate - 5' (methyl carbon 14) by using silylated and lithiated derivatives. The author also reports preliminary studies of biological studies of the trimethylsilyl-5-uridine and of the iodine-6-thymine

  7. Model study of atmospheric transport using carbon 14 and strontium 90 as inert tracers

    Science.gov (United States)

    Kinnison, D. E.; Johnston, H. S.; Wuebbles, D. J.

    1994-10-01

    The observed excess carbon 14 in the atmosphere from 1963 to 1970 provides unique, but limited, data up to an altitude of about 35 km for testing the air motions calculated by 11 multidimensional atmospheric models. Strontium 90 measurements in the atmosphere from 1964 to mid-1967 provide data that have more latitude coverage than those of carbon 14 and are useful for testing combined models of air motions and aerosol settling. Model calculations for carbon 14 begin at October 1963, 9 months after the conclusion of the nuclear bomb tests; the initial conditions for the calculations are derived by three methods, each of which agrees fairly well with measured carbon 14 in October 1963 and each of which has widely different values in regions of the stratosphere where there were no carbon 14 measurements. The model results are compared to the stratospheric measurements, not as if the observed data were absolute standards, but in an effort to obtain new insight about the models and about the atmosphere. The measured carbon 14 vertical profiles at 31°N are qualitatively different from all of the models; the measured vertical profiles show a maximum mixing ratio in the altitude range of 20 to 25 km from October 1963 through July 1966, but all modeled profiles show mixing ratio maxima that increase in altitude from 20 km in October 1963 to greater than 40 km by April 1966. Both carbon 14 and strontium 90 data indicate that the models differ substantially among themselves with respect to stratosphere-troposphere exchange rate, but the modeled carbon 14 stratospheric residence times indicate that differences among the models are small with respect to transport rate between the middle stratosphere and the lower stratosphere. Strontium 90 data indicate that aerosol settling is important up to at least 35 km altitude. Relative to the measurements, about three quarters of the models transport carbon 14 from the lower stratosphere to the troposphere too rapidly, and all models

  8. Behavior of environmental carbon-14 and tritium in Japan

    International Nuclear Information System (INIS)

    Iwakura, T.; Kasida, Y.; Inoue, Y.; Tanaka, K.; Arai, K.

    1979-01-01

    The 14 C activity in plants began to rise appreciably above normal in 1957, and the level rose almost linearly with the rate of 7% per year to the level in 1959. Steep increase of the level to a peak in 1963, between 85% and 90% above normal, shows the effect of large scale nuclear explosions through the end of 1962. Liquid scintillation counting was used as a sensitive assay method of 14 C and 3 H. For 14 C determination, the naturally incorporated 14 C into alcohol and essential oils (thymol, menthol and lemongrass oil) and used, and water samples were used for 3 H measurement. The total amount 65 x 10 27 of 14 C atoms has been produced in nuclear tests, and this amount is about 3% of the total amount of 14 C in nature. The 3 H concentration in rivers, streams and ponds decreased exponentially from 600 pCi/l in 1967 to 150 pCi/l in 1972, with the half life of 2.5yr. The difference of the 3 H concentration in surface water according to the sampling locations implies geographical and meteorological variations in fallout 3 H level. It is said conclusively that environmental waters in Japan have not been influenced by the discharge effluent of the facilities with regard to tritium contamination and that tritium content in precipitation still play an important role in reflecting annual variation of tritium concentration to surface waters. (J.P.N.)

  9. Determination of 14C age of inorganic and organic carbon in ancient Siberian permafrost

    Science.gov (United States)

    Onstott, T. C.; Liang, R.; Lau, M.; Vishnivetskaya, T. A.; Lloyd, K. G.; Pfiffner, S. M.; Hodgins, G.; Rivkina, E.

    2017-12-01

    Permafrost represents a large reservoir of ancient carbon that could have an important impact on the global carbon budget during climate warming. Due to the low turnover rate of carbon by microorganisms at subzero temperatures, the persistence of ancient carbon in younger permafrost deposits could also pose challenges for radiocarbon dating of permafrost sediment. We utilized Accelerator Mass Spectrometry to determine the 14C age of inorganic carbon, labile and recalcitrant organic carbon in Siberian permafrost sediment sampled at various depths from 2.9 to 5.6m. The fraction of inorganic carbon (CO2) was collected after acidification using phosphoric acid. The labile (younger) and recalcitrant (old) organic carbon in the subsequent residues were collected after combustion at 400 ºC and 800 ºC, respectively. The percentages of inorganic carbon increased from the youngest (2.9m) to the oldest (5.6m), whereas the fractions for organic carbon varied significantly at different depths. The 14C age determined in the inorganic fraction in the top sample (2.9 m) was 21,760 yr BP and gradually increased to 33,900 yr BP in the relative deeper sediment (3.5 and 5.6 m). Surprisingly, the fraction of "younger" carbon liberated at 400 oC was older than the more recalcitrant and presumably older organic carbon liberated at 800 oC in all cases. Moreover, the 14C age of the younger and older organic carbon fractions did not increase with depth as observed in the carbonate fraction. In particular, the 14C age of the organic carbon in the top sample (38,590-41,700 yr BP) was much older than the deeper samples at depth of 3.5m (18,228-20,158 yr BP) and 5.6m (29,040-38,020 yr BP). It should be noticed that the metabolism of ancient carbon in frozen permafrost may vary at different depths due to the different proportion of necromass and metabolically active microbes. Therefore, additional knowledge about the carbon dynamics of permafrost and more investigation would be required to

  10. Biogenic Carbon Fraction of Biogas and Natural Gas Fuel Mixtures Determined with 14C

    NARCIS (Netherlands)

    Palstra, Sanne W. L.; Meijer, Harro A. J.

    2014-01-01

    This study investigates the accuracy of the radiocarbon-based calculation of the biogenic carbon fraction for different biogas and biofossil gas mixtures. The focus is on the uncertainty in the C-14 reference values for 100% biogenic carbon and on the C-13-based isotope fractionation correction of

  11. Carbon 14 absorption and translocation in sugar cane

    International Nuclear Information System (INIS)

    Pimentel, R.M.M.; Sampaio, E.V.S.; Salcedo, I.H.

    1990-01-01

    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)

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

    International Nuclear Information System (INIS)

    Gruhlke, J.M.; Meyer, G.L.; Neiheisel, J.

    1987-01-01

    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

  13. Synthesis of a polycyclic aromatic hydrocarbon marked with carbon-14: (b, d e f) dibenzo-chrysene 14C-7,14

    International Nuclear Information System (INIS)

    Chatelain, G.

    1965-01-01

    (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) [fr

  14. Carbon-14 as an indicator of CO2 pollution in cities

    International Nuclear Information System (INIS)

    Vogel, J.C.; Uhlitzsch, I.

    1975-01-01

    The combustion of fossil fuels in cities, and especially in industrial areas, releases large quantities of carbon dioxide into the local atmosphere. This carbon dioxide does not contain carbon-14, with the result that the carbon-14 content of the atmospheric carbon dioxide is locally depleted. The degree of depletion provides a measure for the carbon dioxide pollution at the sampling site. Since growing plants represent a convenient average sample of the carbon dioxide in the air, the leaves of deciduous trees can be used for comparing the magnitude of local pollution in different localities during the summer growing period. A series of leaf samples collected in 1973 from Europe, North America and South Africa reveals the expected differences in the degree of pollution. Extreme instances occur in Scholven (Ruhrgebiet, Germany), where the average day-time carbon dioxide content during the summer months is found to be 8.7% above normal, and in Manhatten, New York City, where the corresponding figure is 6.4%. The technique can easily be extended to include the winter months by directly absorbing carbon dioxide in a hydroxide solution during different seasons. The proposed method is sensitive but much less time-consuming than the continuous measurement of the carbon dioxide concentration in the air. It thus lends itself to the monitoring of impact areas of pollution. (author)

  15. Secular variations in carbon-14 and their geophysical implications

    CSIR Research Space (South Africa)

    Vogel

    2002-03-01

    Full Text Available . The identification of the causes and magnitudes of these deviations has created a new too that is contributing to the investigation of different geophysical: phenomena. Variations in the activity of the Sun produce fluctuations of the C-14 level in the atmosphere...

  16. Carbon -14 labelling of terbinafine, an antimycotic agent

    Energy Technology Data Exchange (ETDEWEB)

    Andres, H. (Sandoz Ltd., Basel (Switzerland). Isotope Div.)

    1989-11-01

    Terbinafine is a new antimycotic agent which is currently being tested worldwide in clinical trials. The synthesis of ({sup 14}C)Terbinafine, labelled in the naphthalene methane moiety as well as in the tertiary butyl group is described. The key step of the latter is the aluminium-mediated tertiary butylation of an alkyne. (author).

  17. Carbon -14 labelling of terbinafine, an antimycotic agent

    International Nuclear Information System (INIS)

    Andres, H.

    1989-01-01

    Terbinafine is a new antimycotic agent which is currently being tested worldwide in clinical trials. The synthesis of [ 14 C]Terbinafine, labelled in the naphthalene methane moiety as well as in the tertiary butyl group is described. The key step of the latter is the aluminium-mediated tertiary butylation of an alkyne. (author)

  18. Immobilization of carbon 14 contained in spent fuel hulls through melting-solidification treatment

    International Nuclear Information System (INIS)

    Mizuno, T.; Maeda, T.; Nakayama, S.; Banba, T.

    2004-01-01

    The melting-solidification treatment of spent nuclear fuel hulls is a potential technique to improve immobilization/stabilization of carbon-14 which is mobile in the environment due to its weakly absorbing properties. Carbon-14 can be immobilized in a solid during the treatment under an inert gas atmosphere, where carbon is not oxidized to gaseous form and remains in the solid. A series of laboratory scale experiments on retention of carbon into an alloy waste form was conducted. Metallic zirconium was melted with metallic copper (Zr/Cu=8/2 in weight) at 1200 deg C under an argon atmosphere. Almost all of the carbon remained in the resulting zirconium-copper alloy. (authors)

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

    International Nuclear Information System (INIS)

    Nishizawa, Kunihide; Nagatsu, Toshiharu; Togari, Akifumi; Matsumoto, Shosei

    1991-01-01

    The atmospheric testing of nuclear weapons since 1945 caused a significant increase in the concentration of atmospheric 14 C. The 14 C concentration in plants that assimilate 14 C directly by photosynthesis reflects the atmospheric 14 C 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 14 C concentration which reflects the 14 C concentration in the blood at the time collagen metabolism ceased. The distribution of the 14 C 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 14 C concentration in teeth

  20. 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.

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

    International Nuclear Information System (INIS)

    Schiller, R.

    1973-01-01

    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 14 C, 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 14 C 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) [de

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

    International Nuclear Information System (INIS)

    Blowers, Paul; Caborn, Jane; Dell, Tony; Gingell, Terry; Harms, Arvic; Long, Stephanie; Sleep, Darren; Stewart, Charlie; Walker, Jill; Warwick, Phil E.

    2011-01-01

    An intercomparison exercise to determine the 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 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.

  3. Synthesis of canrenone and related steroids labelled with tritium, carbon-14, and sulfur-35

    International Nuclear Information System (INIS)

    Markos, C.S.; Dorn, C.R.; Zitzwitz, D.J.

    1988-01-01

    The syntheses of [1- 3 H]canrenone, [1- 3 H]spironolactone, [1- 3 H] potassium canrenoate, [22- 14 C]canrenone, [22- 14 C]spironolactone, [22- 14 C]potassium canrenoate, and [ 35 S]spironolactone are reported. Tritium labelled compounds were obtained by catalytic reduction of a 3-keto-1, 4-diene precursor followed by exchange of enolizable label. Carbon-14 compounds were obtained by reaction of a 17-ethynyl steroid with 14 CO 2 . Sulfur-35 spironolactone was synthesized by the in-situ generation of [ 35 S]thiolacetic acid from [ 35 S]sodium sulfide. (author)

  4. Distribution of Δ14C in western North Pacific and tracing carbons of human origin

    International Nuclear Information System (INIS)

    Aramaki, Takafumi; Mizushima, Toshihiko; Togawa, Orihiko; Kuji, Tomoyuki

    2001-01-01

    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. 14 C concentration was calculated from δ 13 C value calculated from the 13 C/ 12 C ratio. 14 C resulting from the nuclear weapon test was calculated by comparing estimated 14 C and real 14 C concentration. It was compared with that in 1970s. 14 Cbomb has dissolved into North Pacific Intermediate Water in Arctic latitude, which has moved to Mid-latitude. (A. Yamamoto)

  5. Characteristics study of a system for carbon 14 dating

    International Nuclear Information System (INIS)

    Oikawa, H.

    1978-01-01

    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 [pt

  6. Carbon-14 behavior in a cement-dominated environment: Implications for spent CANDU resin waste disposal

    International Nuclear Information System (INIS)

    Dayal, R.; Reardon, E.J.

    1994-01-01

    Cement based waste forms and concrete engineered barriers are expected to play a key role in providing 14 C waste containment and control 14 C migration for time periods commensurate with its hazardous life of about 50,000 years. The main thrust of this study was, therefore, to evaluate the performance of cement based waste forms with regard to 14 C containment. Of particular importance are the geochemical processes controlling 14 C solubility and release under anticipated cement dominated low and intermediate level waste repository conditions. Immobilization of carbonate-form exchange resin in grout involves transfer of sorbed 14 CO 3 2- ions, through exchange for hydroxyl ions from the grout slurry, followed by localized precipitation of solid calcium carbonate at the cement/resin interface in the grout matrix. Carbon-14 release behavior can be attributed to the dissolution characteristics and solubility of calcite present in the cement based waste form. The groundwater flow regime can exert a pronounced effect both on the near-field chemistry and the leaching behavior of 14 C. For a cement dominated repository, at relatively low-flow or stagnant groundwater conditions, the alkaline near-field chemical environments inhibits the release of 14 C from the cemented waste form. Under high flow conditions, the near-field environment is characterized by relatively neutral pH conditions which promote calcite dissolution, thus resulting in 14 C release from the waste form

  7. Precision of Carbon-14 analysis in a single laboratory

    International Nuclear Information System (INIS)

    Nashriyah Mat; Misman Sumin; Holland, P.T.

    2009-01-01

    In a single laboratory, one operator has used a Biological Material Oxidizer (BMO) unit to prepare (combust) solid samples before analyzing (counting) the radioactivity by using various Liquid Scintillation Counters (LSCs). The different batches of commercially available solid Certified Reference Material (CRM, Amersham, UK) standards were analyzed depending on the time of analysis over a period of seven years. The certified radioactivity and accuracy of the C-14 standards as cellulose tabs, designated as the Certified Reference Material (CRM), was 5000 + 3% DPM. Each analysis was carried out using triplicate tabs. The medium of counting was commercially available cocktail containing the sorbent solution for the oxidizer gases, although of different batches were used depending on the date of analysis. The mean DPM of the solutions was measured after correction for quenching by the LSC internal standard procedure and subtracting the mean DPM of control. The precisions of the standard and control counts and of the recovery percentage for the CRM were measured as the coefficients of variation (CV), for the C-14 determination over the seven year period. The results from a recently acquired Sample Oxidizer unit were also included for comparison. (Author)

  8. Carbon-14 releases from an unsaturated repository: A senseless but expensive dilemma

    International Nuclear Information System (INIS)

    Pflum, C.G.

    1993-01-01

    The purpose of the US Environmental Protection Agency (EPA) Environmental Standards for the Management and Disposal of Spent Nuclear Fuel, High-Level and Transuranic Radioactive Wastes (40 CFR Part 191 or standards) is to protect public health and safety. The 1985 rule was developed on the basis of the assumption that the repository would be located in a geologic formation that lies below the water table. It is appropriate to examine gaseous releases and transport of pollutants in order to determine site adequacy. When the provisions of the 1985 standard are applied to Yucca Mountain, specifically the limits for carbon-14, we can release in 10,000 years no more than 7,000 curies of carbon-14 in the form of carbon dioxide. Meanwhile, the US Department of Energy (DOE) and others indicate that the repository may release about 8,000 curies of carbon-14 dioxide, an amount that exceeds the standard by 10 to 20 percent. The original basis of the 1985 standards was that, in a site below the water table, the limit for carbon-14 was technically achievable. It was not a standard based on a release level that would prevent a danger to public health. If we examine the danger to public health of the release of 8,000 curies of carbon-14 dioxide during and 8,000-year period, this release would not a pose a significant threat to the average individual. Industry and natural sources release many times this amount of carbon-14 dioxide each year. The question therefore becomes: is it appropriate to spend an additional $3.2 billion on waste packages when the expenditure does not measurably improve the public health?

  9. 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.

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

    International Nuclear Information System (INIS)

    Kinnison, D.E.; Wuebbles, D.J.; Johnston, H.S.

    1992-02-01

    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 K zz and K yy 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 K yy 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

  11. Fate of gaseous tritium and carbon-14 released from buried low-level radioactive waste

    International Nuclear Information System (INIS)

    Striegl, R.G.

    1988-01-01

    Microbial decomposition, chemical degradation, and volatilization of buried low-level radioactive waste results in the release of gases containing tritium ( 3 H) and carbon-14 ( 14 C) to the surrounding environment. Water vapor, carbon dioxide, and methane that contain 3 H or 14 C are primary products of microbial decomposition of the waste. Depending on the composition of the waste source, chemical degradation and volatilization of waste also may result in the production of a variety of radioactive gases and organic vapors. Movement of the gases in materials that surround waste trenches is affected by physical, geochemical, and biological mechanisms including sorption, gas-water-mineral reactions, isotopic dilution, microbial consumption, and bioaccumulation. These mechanisms either may transfer 3 H and 14 C to solids and infiltrating water or may result in the accumulation of the radionuclides in plant or animal tissue. Gaseous 3 H or 14 C that is not transferred to other forms is ultimately released to the atmosphere

  12. Study of a method of detection for natural carbon-14 using a liquid scintillator, recent variations in the natural radio-activity due to artificial carbon-14 (1963); Etude d'une methode de detection du carrons 14 naturel, utilisant un scintillateur liquide - variations recentes de l'activite naturelle dues au carbone 14 artificiel (1963)

    Energy Technology Data Exchange (ETDEWEB)

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

    1963-06-15

    Among the various natural isotopes of carbon, a radioactive isotope, carbon-14, is formed by the action of secondary neutrons from cosmic rays on nitrogen in the air. Until 1950, the concentration of this isotope in ordinary carbon underwent weak fluctuations of about 2-3 per cent. The exact measurement of this concentration 6 X 10{sup 12} Ci/gm of carbon, and of its fluctuations, are difficult and in the first part of this report a highly sensitive method is given using a liquid scintillator. Since 1950 this natural activity has shown large fluctuations because of the carbon-14 formed during nuclear explosions, and in the second part, the evolution in France of this specific activity of carbon in the atmosphere and biosphere is examined. In the last part is studied the local increase in carbon activity in the atmosphere around the Saclay site, an increase caused by the carbon-14 given off as C{sup 14}O{sub 2}, by the reactors cooled partially with exterior air. (author) [French] Parmi les differents isotopes naturels du carbone, un isotope radioactif, le carbone 14, est forme par l'action de neutrons secondaires due aux rayons cosmiques sir l'azote de l'air. Jusqu'en 1950, la concentration de cet isotope dans le carbone ordinaire est soumise a des fluctuations de faible amplitude, de l'ordre de 2 a 3 pour cent. Les mesures precises de cette concentration, 6. 10{sup -12} Ci/g de carbone, et de ses fluctuations sont delicates, et dans la premiere partie de ce rapport, on decrit une methode de detection a grande sensibilite utilisant un scintillateur liquide. Depuis 1950, cette activite naturelle subit des fluctuations importantes dues au carbone 14 forme lors des explosions nucleaires, et dans la seconde partie, on examine l'evolution en France de l'activite specifique du carbone de l'atmosphere et ce la biosphere. Dans la derniere partie, on etudie l'accroissement local de l'activite du carbone de l'air aux environs du site de Saclay, accroissement provoque par le

  13. Study of a method of detection for natural carbon-14 using a liquid scintillator, recent variations in the natural radio-activity due to artificial carbon-14 (1963); Etude d'une methode de detection du carrons 14 naturel, utilisant un scintillateur liquide - variations recentes de l'activite naturelle dues au carbone 14 artificiel (1963)

    Energy Technology Data Exchange (ETDEWEB)

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

    1963-06-15

    Among the various natural isotopes of carbon, a radioactive isotope, carbon-14, is formed by the action of secondary neutrons from cosmic rays on nitrogen in the air. Until 1950, the concentration of this isotope in ordinary carbon underwent weak fluctuations of about 2-3 per cent. The exact measurement of this concentration 6 X 10{sup 12} Ci/gm of carbon, and of its fluctuations, are difficult and in the first part of this report a highly sensitive method is given using a liquid scintillator. Since 1950 this natural activity has shown large fluctuations because of the carbon-14 formed during nuclear explosions, and in the second part, the evolution in France of this specific activity of carbon in the atmosphere and biosphere is examined. In the last part is studied the local increase in carbon activity in the atmosphere around the Saclay site, an increase caused by the carbon-14 given off as C{sup 14}O{sub 2}, by the reactors cooled partially with exterior air. (author) [French] Parmi les differents isotopes naturels du carbone, un isotope radioactif, le carbone 14, est forme par l'action de neutrons secondaires due aux rayons cosmiques sir l'azote de l'air. Jusqu'en 1950, la concentration de cet isotope dans le carbone ordinaire est soumise a des fluctuations de faible amplitude, de l'ordre de 2 a 3 pour cent. Les mesures precises de cette concentration, 6. 10{sup -12} Ci/g de carbone, et de ses fluctuations sont delicates, et dans la premiere partie de ce rapport, on decrit une methode de detection a grande sensibilite utilisant un scintillateur liquide. Depuis 1950, cette activite naturelle subit des fluctuations importantes dues au carbone 14 forme lors des explosions nucleaires, et dans la seconde partie, on examine l'evolution en France de l'activite specifique du carbone de l'atmosphere et ce la biosphere. Dans la derniere partie, on etudie l'accroissement local de l'activite du carbone de l'air aux

  14. 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.)

  15. The synthesis of a tritium, carbon-14, and stable isotope-labeled cathepsin C inhibitors.

    Science.gov (United States)

    Allen, Paul; Bragg, Ryan A; Caffrey, Moya; Ericsson, Cecilia; Hickey, Michael J; Kingston, Lee P; Elmore, Charles S

    2017-02-01

    As part of a medicinal chemistry program aimed at developing a highly potent and selective cathepsin C inhibitor, tritium, carbon-14, and stable isotope-labeled materials were required. The synthesis of tritium-labeled methanesulfonate 5 was achieved via catalytic tritiolysis of a chloro precursor, albeit at a low radiochemical purity of 67%. Tritium-labeled AZD5248 was prepared via a 3-stage synthesis, utilizing amide-directed hydrogen isotope exchange. Carbon-14 and stable isotope-labeled AZD5248 were successfully prepared through modifications of the medicinal chemistry synthetic route, enabling the use of available labeled intermediates. Copyright © 2016 John Wiley & Sons, Ltd.

  16. Coal chemistry. 8. Reactions of tetralin with coal and with some carbon-14-containing model compounds

    International Nuclear Information System (INIS)

    Collins, C.J.; Raaen, V.F.; Benjamin, B.M.; Maupin, P.H.; Roark, W.H.

    1979-01-01

    When coal was treated with tetralin-l- 14 C at 400 0 C, small yields of α- and β-methylnaphthalenes- 14 C were observed. In order to determine the mechanism of the reaction, tetralin was heated with 14 C-labeled 1,3-diphenylpropanes (1), with 1,3-diphenylpropene (2), and with 14 C-labeled phenetoles (3). In each case methylnaphthalenes were observed, and the origins of the methyl groups were determined with carbon-14. In addition to the methylnaphthalenes, 1 and 2 also yielded toluene and ethylbenzene (after 19 h), whereas phenetole-β- 14 C (3-β- 14 C) yielded toluene (unlabeled) plus ethyl- 14 C-benzene, benzene, phenol, and a mixture of α- and β-ethyl- 14 C-naphthalenes. Crossover experiments with labeled phenetole and unlabeled ethyl p-tolyl ether proved the intramolecularity of the reaction phenetole → toluene + ethylbenzene, thus illustrating a 1,2-phenyl shift from oxygen to carbon

  17. Rapid localization of carbon 14-labeled molecules in biological samples by ion mass microscopy

    International Nuclear Information System (INIS)

    Hindie, E.; Escaig, F.; Coulomb, B.; Lebreton, C.; Galle, P.

    1989-01-01

    We report here on the ability of secondary ion mass spectrometry (SIMS) to provide rapid imaging of the intracellular distribution of 14 C-labeled molecules. The validity of this method, using mass discrimination of carbon 14 atoms, was assessed by imaging the distribution of two molecules of well-known metabolism, [ 14 C]-thymidine and [ 14 C]-uridine, incorporated by human fibroblasts in culture. As expected, 14 C ion images showed the presence of [ 14 C]-thymidine in the nucleus of dividing cells, whereas [ 14 C]-uridine was present in the cytoplasm as well as the nucleus of all cells, with a large concentration in the nucleoli. The time required to obtain the distribution images with the SMI 300 microscope was less than 6 min, whereas microautoradiography, the classical method for mapping the tissue distribution of 14 C-labeled molecules, usually requires exposure times of several months. Secondary ion mass spectrometry using in situ mass discrimination is proposed here as a very sensitive method which permits rapid imaging of the subcellular distribution of molecules labeled with carbon 14

  18. Investigations into the post-natal development of demethylating enzyme systems by determination of carbon dioxide 14 in the air exhaled by mice after applications of carbon 14 dimethyl amino-antipyrine

    International Nuclear Information System (INIS)

    Schmidt, H.

    1982-01-01

    Albino mice were subcutaneously injected with carbon 14 dimethyl aminopyrines, the methyl group of which can be metabolised in the organism into carbon dioxide 14. The following results were obtained: In the carbon dioxide 14 exhalation of neonate, young and adult animals after administration of carbon 14 aminopyrine, distinct differences were noted. The maximum of elimination via the lungs occurs after 20-30 minutes in grown-up mice, in neonates or young animals distinctly later (60-90 min). The carbon dioxide 14 exhalation was also measured after additional subcutaneous application of methrotrexate. In mice aged 8 and 10 days a distinct decrease in carbon dioxide 14 exhalation was found. By contrast, a rise in carbon dioxide 14 exhaled was found in mice aged 2 days. The orientating experiments with folic acid and carbon 14 dimethyl aminopyrine show that leucovorin leads to a distinct increase in carbon dioxide 14 exhalation during the first 30 minutes. As a cause of the different degrees of stimulation respectively inhibition of demethylation, different biochemical ways of formaldehyde formation are pointed out. One of these probably includes the folate-dependent reaction. (orig./MG) [de

  19. 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

  20. Laboratory Experiments to Evaluate Diffusion of 14C into Nevada Test Site Carbonate Aquifer Matrix

    Energy Technology Data Exchange (ETDEWEB)

    Ronald L. Hershey; William Howcroft; Paul W. Reimus

    2003-03-01

    Determination of groundwater flow velocities at the Nevada Test Site is important since groundwater is the principal transport medium of underground radionuclides. However, 14C-based groundwater velocities in the carbonate aquifers of the Nevada Test Site are several orders of magnitude slower than velocities derived from the Underground Test Area regional numerical model. This discrepancy has been attributed to the loss or retardation of 14C from groundwater into the surrounding aquifer matrix making 14C-based groundwater ages appear much older. Laboratory experiments were used to investigate the retardation of 14C in the carbonate aquifers at the Nevada Test Site. Three sets of experiments were conducted evaluating the diffusion of 14C into the carbonate aquifer matrix, adsorption and/or isotopic exchange onto the pore surfaces of the carbonate matrix, and adsorption and/or isotopic exchange onto the fracture surfaces of the carbonate aquifer. Experimental results a nd published aquifer matrix and fracture porosities from the Lower Carbonate Aquifer were applied to a 14C retardation model. The model produced an extremely wide range of retardation factors because of the wide range of published aquifer matrix and fracture porosities (over three orders of magnitude). Large retardation factors suggest that groundwater with very little measured 14C activity may actually be very young if matrix porosity is large relative to the fracture porosity. Groundwater samples collected from highly fractured aquifers with large effective fracture porosities may have relatively small correction factors, while samples from aquifers with a few widely spaced fractures may have very large correction factors. These retardation factors were then used to calculate groundwater velocities from a proposed flow path at the Nevada Test Site. The upper end of the range of 14C correction factors estimated groundwater velocities that appear to be at least an order of magnitude too high compared

  1. ORIGIN OF PALMITIC ACID CARBON IN PALMITATES FORMED FROM HEXADECANE-1-C14 AND TETRADECANE-1-C14 BY MICROCOCCUS CERIFICANS

    Science.gov (United States)

    Finnerty, W. R.; Kallio, R. E.

    1964-01-01

    Finnerty, W. R. (University of Iowa, Iowa City), and R. E. Kallio. Origin of palmitic acid carbon in palmitates formed from hexadecane-1-C14 and tetradecane-1-C14 by Micrococcus cerificans. J. Bacteriol. 87:1261–1265. 1964.—Degradation of the palmitic acid moiety of cetyl palmitate and myristyl palmitate formed from hexadecane-1-C14 and tetradecane-1-C14 by Micrococcus cerificans was carried out. The patterns of C14 labeling in palmitic acid from cetyl palmitate showed that hexadecane is oxidized at the C1 position, and cetyl alcohol and palmitic acid thus formed are directly esterified. Palmitic acid arising from tetradecane and esterified to tetradecanol appeared to have been synthesized by the addition of two carbon atoms to an existing 14-carbon atom skeleton. Considerable mixing of C14 occurred in the C1 and C2 positions of palmitic acid thus synthesized. PMID:14188700

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

    International Nuclear Information System (INIS)

    Loheac, J.

    1966-06-01

    Several new syntheses of δ aminolevulic acid (δ A.L.A.) have been studied. 14 C-4 δ - aminolevulic acid has been obtained from 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 14 C-1 or 14 C-2 δ-A.L.A. has been prepared from the 14 C-1 or 14 C-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) [fr

  3. Carbon-14 urea utilization in diagnosis of the presence Campylobacter pylori in stomach

    International Nuclear Information System (INIS)

    Chausson, Y.

    1989-01-01

    A new method to detect the Campylobacter pylori in the stomach, using carbon-14 urea is presented. The technique consists in after the tracer ingestion, the tracer is recuperated by the expiration way in organic hiamin and after counting and evaluating. (M.L.J.)

  4. The leachability of carbon-14-labelled 3,4-benzopyrene from coal ash into aqueous systems

    NARCIS (Netherlands)

    Besemer, A.C.; Kanij, J.

    1984-01-01

    The leachability of polycyclic aromatic hydrocarbons from coal ash into aqueous systems was studied. Carbon-14-labeled 3,4-Benzopyrene (BaP) was deposited on coal fly ash by adsorption from the liquid phase in quantities of about 10 ??g/g ash. After a thermal treatment in air at 120??C for 2 hours

  5. New method of radiation measurement at carbon isotope 14 low level in an environmental atmospheric sampling

    International Nuclear Information System (INIS)

    Tormos, J.

    2009-01-01

    A new method of preparation is proposed to extract the atmospheric carbon trapped in the solution of soda coming from air sampling in environment with a carbon-14 bubbler (type H.A.G. 7000). It is based on the neutralisation of the global soda solution got from bubbling pots by nitric acid, the complete desorption of the carbon under gaseous oxidized form (CO 2 ) and its trapping in a only capacity containing a reactive. The whole of the device is scanned by air at steady rate. A test catch of the reactive and of the trapped carbon dioxide is then blended to a glistening liquid (Permafluor E+) and measured in beta counting by scintillation in liquid medium with a counter for the measurement of low energy beta emitters at very low level of activity (Quantulus type). this method allows to get a limit of detection equal to 5 mBq/m 3 for the atmospheric organic carbon. The principal interest of this method is its quickness and simplicity of setting in motion for a measurement of 14 C in the atmospheric carbon dioxide at a level of natural activity. (N.C.)

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

    International Nuclear Information System (INIS)

    Jayasekara, K.S.; Jayaswkara, K.S.; Bowen, G.D.

    2000-01-01

    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

  7. Carbon-14 kinetic isotope effects and mechanisms of addition of 2,4-dinitrobenzenesulfenyl chloride to substituted styrenes-1-14C and styrenes-2-14C

    International Nuclear Information System (INIS)

    Kanska, M.; Fry, A.

    1983-01-01

    As the first reported examples of carbon isotope effects in simple electrophilic addition reactions we have measured the carbon-14 kinetic isotope effects in the addition of 2,4-dinitrobenzenesulfenyl chloride to a series of para-substituted α and β-labeled styrenes in acetic acid at 30.1 0 C: for para substituents Cl, H, and CH 3 the k/ 14 K values for α labeling are 1.027, 1.022, and 1.004, and the k/ 14 k values for β labeling are 1.035, 1.032, and 1.037, all +/-approx.0.004. The kinetics of the reaction were measured for the p-CH 3 O,p-CH 3 , unsubstituted, p-Cl, and m-NO 2 styrenes; electron-donating groups strongly accelerate the reaction, and electron-withdrawing groups retard it. The Hammett plot is curved with p + values ranging from about -4.6 at the electron-donating group (EDG) end to about -1.8 at the electron-withdrawing group (EWG) end. Both the isotope effect and kinetic data, and related data from the literature, are interpreted in terms of a changing mechanism, with the activated complexes of the rate-determining steps having much open carbenium ion (ion pair) character for EDG-substituted styrenes and much cyclic thiiranium io (ion par) character for EWG-substituted styrenes. 1 figure, 2 tables

  8. Carbon-14 speciation during anoxic corrosion of activated steel in a repository environment

    Energy Technology Data Exchange (ETDEWEB)

    Wieland, E.; Cvetkovic, B.Z.; Kunz, D. [Paul Scherrer Institute, Villigen (Switzerland). Lab. for Waste Management; Salazar, G.; Szidat, S. [Bern Univ. (Switzerland). Dept. of Chemistry and Biochemistry and Oeschger Centre for Climate Change Research

    2018-01-15

    Radioactive waste contains significant amounts of {sup 14}C which has been identified a key radionuclide in safety assessments. In Switzerland, the {sup 14}C inventory of a cement-based repository for low- and intermediate-level radioactive waste (L/ILW) is mainly associated with activated steel (∝85 %). {sup 14}C is produced by {sup 14}N activation in steel parts exposed to thermal neutron flux in light water reactors. Release of {sup 14}C occurs in the near field of a deep geological repository due to anoxic corrosion of activated steel. Although the {sup 14}C inventory of the L/ILW repository and the sources of {sup 14}C are well known, the formation of {sup 14}C species during steel corrosion is only poorly understood. The aim of the present study was to identify and quantify the {sup 14}C-bearing carbon species formed during the anoxic corrosion of iron and steel and further to determine the {sup 14}C speciation in a corrosion experiment with activated steel. All experiments were conducted in conditions similar to those anticipated in the near field of a cement-based repository.

  9. The interaction of carbon-14 carbonate solution species with semiarid sediment

    International Nuclear Information System (INIS)

    Martin, W.J.

    1991-10-01

    14 C is a waste product that has been and may continue to be disposed and/or released into our environment. Subsurface land disposal has been considered as a means of control of nuclear waste and disposal of contaminant migration in the environment. Semiarid environments are preferred for subsurface disposal of solid and liquid wastes. However, such disposal of 14 C may potentially introduce it into the subsurface and groundwater environmental pathways. A limited amount of site-specific data have been published for 14 C transport through the subsurface and groundwater pathways. The experiments conducted in this study perform two functions: (1) they provide a specific impetus for further experimental work and (2) they give credibility to the estimated values used in environmental dose modeling. 11 refs., 1 fig., 1 tab

  10. An integrated approach to geological disposal of UK wastes containing carbon-14

    International Nuclear Information System (INIS)

    Vines, Sarah; Lever, David

    2013-01-01

    Carbon-14 is a key radionuclide in the assessment of the safety of a geological disposal facility for radioactive waste because of the calculated assessment of the radiological consequences of gaseous carbon-14 bearing species [i]. It may be that such calculations are based on overly conservative assumptions and that better understanding could lead to considerably reduced assessment of the radiological consequences from these wastes. Alternatively, it may be possible to mitigate the impact of these wastes through alternative treatment, packaging or design options. The Radioactive Waste Management Directorate of the UK's Nuclear Decommissioning Authority (NDA RWMD) has established an integrated project team in which the partners are working together to develop a holistic approach to carbon-14 management in the disposal system [ii]. For a waste stream containing carbon-14 to be an issue: There must be a significant inventory of carbon-14 in the waste stream; and That waste stream has to generate carbon-14 bearing gas; and a bulk gas phase has to entrain the carbon-14 bearing gas: and these gases must migrate through the engineered barriers in significant quantities; and these gases must migrate through the overlying geological environment (either as a distinct gas phase or as dissolved gas); and these gases must interact with materials in the biosphere (i.e. plants) in a manner that leads to significant doses and risks to exposed groups or potentially exposed groups. The project team has developed and used this 'and' approach to structure and prioritise the technical work and break the problem down in a manageable way. We have also used it to develop our approach to considering alternative treatment, packaging and design options. For example, it may be possible to pre-treat some wastes to remove some of the inventory or to segregate other wastes so that they are removed from any bulk gas phase which might facilitate migration through the geosphere

  11. An integrated approach to geological disposal of UK wastes containing carbon-14

    Energy Technology Data Exchange (ETDEWEB)

    Vines, Sarah [Nuclear Decommissioning Authority, Harwell, Oxfordshire (United Kingdom); Lever, David [AMEC, Harwell, Oxfordshire (United Kingdom)

    2013-07-01

    Carbon-14 is a key radionuclide in the assessment of the safety of a geological disposal facility for radioactive waste because of the calculated assessment of the radiological consequences of gaseous carbon-14 bearing species [i]. It may be that such calculations are based on overly conservative assumptions and that better understanding could lead to considerably reduced assessment of the radiological consequences from these wastes. Alternatively, it may be possible to mitigate the impact of these wastes through alternative treatment, packaging or design options. The Radioactive Waste Management Directorate of the UK's Nuclear Decommissioning Authority (NDA RWMD) has established an integrated project team in which the partners are working together to develop a holistic approach to carbon-14 management in the disposal system [ii]. For a waste stream containing carbon-14 to be an issue: There must be a significant inventory of carbon-14 in the waste stream; and That waste stream has to generate carbon-14 bearing gas; and a bulk gas phase has to entrain the carbon-14 bearing gas: and these gases must migrate through the engineered barriers in significant quantities; and these gases must migrate through the overlying geological environment (either as a distinct gas phase or as dissolved gas); and these gases must interact with materials in the biosphere (i.e. plants) in a manner that leads to significant doses and risks to exposed groups or potentially exposed groups. The project team has developed and used this 'and' approach to structure and prioritise the technical work and break the problem down in a manageable way. We have also used it to develop our approach to considering alternative treatment, packaging and design options. For example, it may be possible to pre-treat some wastes to remove some of the inventory or to segregate other wastes so that they are removed from any bulk gas phase which might facilitate migration through the geosphere

  12. Physiological conditions and uptake of inorganic carbon-14 by plant roots

    International Nuclear Information System (INIS)

    Amiro, B.D.; Ewing, L.L.

    1992-01-01

    The uptake of inorganic 14 C by bean plant roots was measured. The plants were grown in a nutrient solution culture at pH 6 and a NaH 14 CO 3 tracer was added to the growth medium. Photosynthesis and transpiration were varied by exposing the aerial portions of the plants to different atmospheric CO 2 concentrations, humidities and light levels in a cuvette system. Leaf concentrations of 14 C were measured at the end of the experiments using liquid scintillation counting. Plant uptake of 14 C via the roots was independent of the photosynthetic rate and, in most cases, could be predicted by knowing the transpiration rate and the nutrient solution concentration. However, when a less efficient root-medium aeration system was used, 14 C uptake was greater than that predicted using transpiration, a phenomenon observed by other researchers. This contrasted to results of another experiment where the measured uptake of iodine was much slower than that predicted using transpiration. Knowledge of transpiration rates is useful in predicting inorganic carbon uptake via the roots and in estimating 14 C transport from contaminated soils to biota. Also, the independence of the uptake from photosynthesis and ambient CO 2 concentrations suggests that future increases in atmospheric CO 2 concentrations may not have a direct effect on root uptake of soil carbon. (author)

  13. Effect of fasting and different diets on 14C incorporation from U-14C glucose into glycogen and carbon dioxide by cerebral cortical slices of rats

    International Nuclear Information System (INIS)

    Visweswaran, P.; Binod Kumar; Sinha, A.P.; Suraiya, A.; Brahamchari, A.K.; Singh, S.P.

    1994-01-01

    There are some reports regarding change in the glycogen level due to fasting. Here an attempt is made by keeping the albino rats under fasting or feeding different diets on the rate of 14 C incorporation into glycogen and carbon dioxide from U- 14 C glucose. Our study reveals that the above conditions do not alter any significant change in the glycogen and carbon dioxide in the cerebral cortical slices of albino rats. (author). 8 refs., 1 tab

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

    International Nuclear Information System (INIS)

    Seidl, P.A.

    1985-02-01

    Cross sections for the /sup 13,14/C, 26 Mg, 56 Fe(π + ,π - )/sup 13,14/O, 26 Si, 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 π/ 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 14 O(0 + , 5.92 MeV), 14 O(2 + , 7.77 MeV), 56 Ni(gs), 13 O(gs), and 13 O(4.21 MeV) are presented. The 13 O(4.21 MeV) state is postulated to have J/sup π/ = 1/2 - . 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 Δ 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 π/ > 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

  15. Carbonate as sputter target material for rapid {sup 14}C AMS

    Energy Technology Data Exchange (ETDEWEB)

    Longworth, Brett E., E-mail: blongworth@whoi.edu [Department of Geology and Geophysics, Woods Hole Oceanographic Institution, Woods Hole, MA (United States); Robinson, Laura F. [Department of Marine Chemistry and Geochemistry, Woods Hole Oceanographic Institution, Woods Hole, MA (United States); Roberts, Mark L.; Beaupre, Steven R.; Burke, Andrea [Department of Geology and Geophysics, Woods Hole Oceanographic Institution, Woods Hole, MA (United States); Jenkins, William J. [Department of Marine Chemistry and Geochemistry, Woods Hole Oceanographic Institution, Woods Hole, MA (United States)

    2013-01-15

    This paper describes a technique for measuring the {sup 14}C content of carbonate samples by producing C{sup -} ions directly in the negative ion sputter source of an accelerator mass spectrometer (AMS) system. This direct analysis of carbonate material eliminates the time and expense of graphite preparation. Powdered carbonate is mixed with titanium powder, loaded into a target cartridge, and compressed. Beam currents for optimally-sized carbonate targets (0.09-0.15 mg C) are typically 10-20% of those produced by optimally-sized graphite targets (0.5-1 mg C). Modern (>0.8 Fm) samples run by this method have standard deviations of 0.009 Fm or less, and near-modern samples run as unknowns agree with values from traditional hydrolysis/graphite to better than 2%. Targets with as little as 0.06 mg carbonate produce useable ion currents and results, albeit with increased error and larger blank. In its current state, direct sputtering is best applied to problems where a large number of analyses with lower precision are required. These applications could include age surveys of deep-sea corals for determination of historic population dynamics, to identify samples that would benefit from high precision analysis, and for growth rate studies of organisms forming carbonate skeletons.

  16. CO2-laser decomposition method of carbonate for AMS 14C measurements

    International Nuclear Information System (INIS)

    Kitagawa, Hiroyuki

    2013-01-01

    A CO 2 laser decomposition method enabled the efficient preparation of carbonate samples for AMS 14 C measurement. Samples were loaded in a vacuum chamber and thermally decomposed using laser emission. CO 2 liberated from the carbonate was directly trapped in the cold finger trap of a small CO 2 reduction reactor and graphitized by a hydrogen gas reduction method using catalytic iron powder. The fraction modern values for 0.07–0.57 mg of carbon, obtained from 200 μm-diameter spots of IAEA-C1, varied with sample size in the range of 0.00072 ± 0.00003 to 0.00615 ± 0.00052. The contamination induced by the laser decomposition method and the following graphite handling was estimated to be 0.53 ± 0.21 μg of modern carbon, assuming a constant amount of extraneous carbon contamination. This method could also make it possible to avoid the time-consuming procedures of the conventional acid dissolution method that involves multiple complex steps for the preparation of carbonate samples.

  17. Sampling and monitoring of carbon-14 in gaseous effluents from nuclear facilities - a literature survey

    International Nuclear Information System (INIS)

    Snellman, M.

    1988-12-01

    C-14 compounds produced in the coolant may be released mainly together with off-gas and waste water from the coolant purification and treatment system. In reactors the release of C-14 will occur mainly in gaseous effluents and only a few percent in liquid effluents. Reported releases from BWRs range from 260 to 670 GBq/GW(e) x year and from 90 to 430 GBq/GW(e) x year for PWRs. At BWRs the condenser air ejector contributes the main inplant release pathway, whereas in PWRs the off-gas treatment vents are the main pathway for C-14 release. C-14 sampling methods depend generally on the C-14 being in the form of CO 2 . The off-gas discharges from BWRs are mainly in the form of CO 2 whereas in PWRs a major fraction of the released C-14 is in the form of hydrocarbons or carbon monoxide (generally 80-100%). Sampling systems in PWRs should therefore be equipped with a catalytic oxidizer to convert all C-14 to CO 2 before trapping. The purpose of this study is to provide information on the techniques available for sampling and monitoring C-14

  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

    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...... 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......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. Requirements for controlling a repository's releases of carbon-14 dioxide; the high costs and negligible benefits

    International Nuclear Information System (INIS)

    Park, U Sun; Pflum, C.G.

    1990-01-01

    A repository excavated within the unsaturated zone may release carbon (C)-14 dioxide in amounts that exceed limits imposed by the Environmental Protection Agency (EPA) and the Nuclear Regulatory Commission (NRC). The release would not threaten the general population, but may expose some hypothetical maximally exposed individual to 0.0005 millirems/year. Yet a repository's releases of C-14 dioxide are strictly regulated, perhaps unintentionally. The EPA and NRC regulations could force the Department of Energy to design and fabricate an expensive 10,000-year waste package solely for the sake of controlling releases of C-14 dioxide. This paper argues that the repository regulations should exempt releases of C-14 dioxide or at least impose more equitable limits. 21 refs., 1 tab

  20. Study of the behaviour of organic carbon in the soil, and carbon 14 study of podzols; Contribution a l'etude du comportement du carbone organique dans le sol et etude des podzols a l'aide du carbone 14

    Energy Technology Data Exchange (ETDEWEB)

    Nakhla Shawki, M [Commissariat a l' Energie Atomique, Saclay (France). Centre d' Etudes Nucleaires

    1969-07-01

    Using the penetration into soil of carbon 14 of thermo-nuclear origin, the behaviour and renewal rate were studied on different organic fractions of the soil. It was established that 18% of the total organic matter is renewed in about 400 years. In addition the formation of podzol-type fossil soils in France was dated from the first millenary B.C., i.e. the end of the sub-boreal period and the beginning of the atlantic period. (author) [French] En utilisant la penetration dans le sol du carbone 14 d'origine thermonucleaire, on a etudie le comportement et la vitesse de renouvellement des differentes fractions de la matiere organique du sol. On a pu preciser que 18% de la matiere organique globale se renouvelait en 400 ans environ. Par ailleurs, la formation en France des sols fossiles du type podzol a ete datee du premier millenaire avant J.C. c'est a dire a la fin de la periode subboreale et au debut de la periode atlantique. (auteur)

  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. Synthesis of carbon-14-labeled sodium palmoxirate and its coenzyme A ester

    Energy Technology Data Exchange (ETDEWEB)

    Weaner, L.E.; Hoerr, D.C.

    1986-04-01

    Synthetic procedures for the preparation of carbon-14-labeled sodium palmoxirate (TDGA), labeled either in the carboxyl position or in the tetradecyl hydrocarbon chain, are described. In addition, the synthesis of the coenzyme A ester of TDGA-14C with a specific activity of 51 mCi/mmol is reported. The coenzyme A ester was prepared by formation of the acyl chloride with oxalyl chloride followed by reaction with coenzyme A (CoA) in a borate-buffered tetrahydrofuran solution. Purification methods and analytical and stability data are reported for the compounds.

  3. First accelerator carbon-14 date for pigment from a rock painting

    International Nuclear Information System (INIS)

    Van der Merwe, N.J.; Sealy, J.; Yates, R.

    1987-01-01

    South Africa is particularly blessed with rock art: thousands of paintings and engravings provide a window on the cognitive systems of prehistoric populations. A major stumbling block in studying the art is the lack of a method for dating it. This article shows that some of the paintings can be directly dated by means of accelerator 14 C counting of carbon from black pigment. The advent of accelerator 14 C provides the capability of analysing very small samples and brings pigments from rock paintings into the realm of datable materials

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

    International Nuclear Information System (INIS)

    Haag, G.L.

    1980-01-01

    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 CO 2 -Ba(OH) 2 hydrate gas-solid reaction to directly remove and immobilize carbon-14. The reaction product, BaCO 3 , 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 CO 2 ) gas streams. For the treatment of an air-based off-gas stream, the use of packed beds of Ba(OH) 2 .8H 2 O flakes to remove CO 2 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 .8H 2 O, 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 .8H 2 O to BaCO 3 and not from the hydration of the commercial Ba(OH) 2 .8H 2 O (i.e. Ba(OH) 2 .7.50H 2 O) to Ba(OH) 2 .8H 2 O

  5. The synthesis of tritium, carbon-14 and stable isotope labelled selective estrogen receptor degraders.

    Science.gov (United States)

    Bragg, Ryan A; Bushby, Nick; Ericsson, Cecilia; Kingston, Lee P; Ji, Hailong; Elmore, Charles S

    2016-09-01

    As part of a Medicinal Chemistry program aimed at developing an orally bioavailable selective estrogen receptor degrader, a number of tritium, carbon-14, and stable isotope labelled (E)-3-[4-(2,3,4,9-tetrahydro-1H-pyrido[3,4-b]indol-1-yl)phenyl]prop-2-enoic acids were required. This paper discusses 5 synthetic approaches to this compound class. Copyright © 2016 John Wiley & Sons, Ltd.

  6. Effect of IX column maintenance on carbon-14 concentration in moderator systems

    International Nuclear Information System (INIS)

    Gallagher, C.L.; Tripple, A.W.

    2006-01-01

    The radionuclide 14 C is produced in CANDU reactors primarily by the (n,α) reaction with 17 O. Because of high neutron fluxes in the core, the majority of the 14 C (94.5%) is produced in the moderator. In the moderator system, 14 C is present mainly as CO 2 in the cover gas in dynamic equilibrium with dissolved carbonates, bicarbonates and CO 2 in the moderator water. Emissions of 14 C from reactors occur through venting or leakage of the cover gas. By controlling the dissolved carbonates in the moderator water with an ion exchange (IX) purification system, the amount of 14 C in the cover gas is minimized and thus the emissions of 14 C can be reduced. A study was conducted to measure the 14 C concentrations in the moderator system at Gentilly 2 in order to determine the effectiveness of the purification system in removing 14 C. Moderator water samples were obtained from the inlet and outlet of the purification system from 2004 January 14 to July 12, covering the operation of two IX columns (IX-1 and IX-3). The moderator water samples contained high levels of tritium (∼2 TBq·L -1 ). As both tritium and 14 C are β-radiation emitters, direct counting of moderator water for 14 C is impossible as the signal due to tritium dominates over that of other β-emitters. Therefore, a procedure developed by Caron et al. was used in this study, which involved acidifying the sample to release the dissolved 14 CO 2 as gas and collecting the 14 CO 2 in a base (NaOH), which could then be measured by liquid scintillation counting to determine the 14 C concentration. Both of the IX columns started with 14 C removal efficiencies of about 95%. The efficiency began to decrease almost immediately with the IX-1 column dropping to 80% efficiency after ∼1115 hours. This drop in efficiency also led to an increase in the inlet concentration over time. IX-1 column was removed from service after ∼1745 hours with a 14 C removal efficiency of ∼31%. IX-3 column was then placed in service

  7. The use of barytocalcite for carbon 14 immobilization: One-year leaching behavior

    Energy Technology Data Exchange (ETDEWEB)

    Massoni, Nicolas, E-mail: nicolas.massoni@cea.fr; Marcou, Céline; Rosen, Jérémy; Jollivet, Patrick

    2014-11-15

    The spent nuclear fuel reprocessing process is one of the anthropogenic sources of carbon-14, and since this element is highly mobile in the geosphere, its sequestration is necessary. Several phases and industrial solutions to immobilize this radionuclide have been studied, including the barytocalcite phase BaCa(CO{sub 3}){sub 2} at 8.08 wt.% of C, which has many advantages such as its low specific volume of carbon. Recently, different options to synthesize this phase have been reported. Here we report on the aqueous durability of barytocalcite, studied for one year with pure water at 30 °C, in order to complete the behavior studies. Unexpected leaching behavior was encountered: it had been supposed that barytocalcite would only leach slowly, but after 1 year, it was no longer present. It appears that its simple CaCO{sub 3} and BaCO{sub 3} constituents precipitated, though the overall carbon loss was low during the period studied. This research gives a new insight into the behavior of this phase regarding carbon-14 immobilization.

  8. Applications of environmental tritium and carbon-14 in water resources investigation in Taiyuan region China

    International Nuclear Information System (INIS)

    Cai Zuhuang; Shi Huixin

    1988-01-01

    To evaluate the influence of exploiting karst groundwater by 0.5-1 cubic metre per second by Gujiao Coal Mine on the discharge rate of the major Lancun spring, Jinci spring and Xizhang waterworks in the Taiyuan region, Shanxi Province, and to seek new sources of water to make up for this influence, we carried out systematic hydrogeological studies in this region from 1983 to 1986, including measurement of 180 data of tritium, 49 data of carbon-13, 20 data of carbon-14, as well as more than 2,000 chemical data. Isotopic and chemical data were interpreted and used to distinguish the groundwater system, to determine the mixing ratios of various groundwaters, to trace the movement of groundwater both inside each subsystem and from one subsystem to another. Groundwater ages at 13 sites in the studied region were obtained after correction for mixing with young water, correction for dilution by dead carbon, and correction for variation of initial carbon-14 concentration. The velocity of groundwater flow was determined on the basis of groundwater ages. (author). 3 figs, 5 tabs

  9. Measurement of the carbon 14 activity at natural level in air samples

    International Nuclear Information System (INIS)

    Olivier, A.; Tenailleau, L.; Baron, Y.; Maro, D.

    2004-01-01

    The aim of the study was to measure the carbon 14 activity at natural level in air samples using classical methods of radiochemistry and beta counting. Three different methods have been tested in order to minimise the detection limit. In the three methods, the first step consists in trapping the atmospheric carbon 14 into NaOH (1N) using a bubbling chamber. The atmospheric carbon dioxide reacts with NaOH to form Na 2 CO 3 . In the first method the Na 2 CO 3 solution is mixed with a liquid scintillate and is directly analysed by liquid scintillation counting (LSC). The detection limit is approximately 1 Bq/m 3 of air samples. The second method consists in evaporating the carbonate solution and then counting the solid residue with a proportional gas circulation counter. The detection limit obtained is lower than the first method (0.4 Bq/m 3 of air samples). In the third method, Na 2 CO 3 is precipitated into CaCO 3 in presence of CaCl 2 . CaCO 3 is then analysed by LSC. This method appear to be the most appropriate, the detection limit is 0.05 Bq/m 3 of air samples. (author)

  10. Proportion of biogenic carbon in flue gas by carbon-14 measurement

    International Nuclear Information System (INIS)

    Lehtomaeki, J.; Antson, O.; Hongisto, M.; Knuuttila, M.; Roine, J.; Raesaenen, J.; Tormonen, K.; Jungner, H.

    2007-01-01

    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.)

  11. 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.)

  12. Synthesis of puric bases labelled with carbon 14 and nitrogen 15

    International Nuclear Information System (INIS)

    Lamorre, Yves

    1975-01-01

    In this report for graduation in organic chemistry engineering, the author reports the synthesis of adenine 14 C-2 et 14 C-6 by two different chemical ways from two derivatives of imidazole. He has used adenine 14 C-6 to obtain hypoxanthine 14 C-6, and then, by enzymatic processing, uric acid 14 C-6. He reports the study of the production of guanine 14 C-2 by cyclization of silylated derivative of imidazole with the carbon 14 C sulphur. However, a method of complete synthesis of this same compound revealed to be more practical. This complete synthesis way allowed the labelling of guanine in positions 1, 2 and 3 by the 96 per cent isotopic nitrogen. Nitrogen in positions 7 and 9 could have been labelled by the same way from the ethyl cyanoacetate 15 N and from the sodium nitrite 15 N. The study of the mass spectrum of these compounds labelled with nitrogen 15 N allowed most of fragments obtained during this analysis to be identified [fr

  13. Carbon-14 dynamics in rice: an extension of the ORYZA2000 model

    Energy Technology Data Exchange (ETDEWEB)

    Galeriu, D.; Melintescu, A. [' ' Horia Hulubei' ' National Institute for Physics and Nuclear Engineering, Life and Environmental Physics Department, 30 Reactorului St., POB MG-6, Bucharest-Magurele (Romania)

    2014-03-15

    Carbon-14 ({sup 14}C) is a radionuclide of major interest in nuclear power production. The Fukushima accident changed the public attitude on the use of nuclear energy all over the world. In terms of nuclear safety, the need of quality-assured radiological models was emphasized by many international organizations, and for models used by decision-makers (i.e. regulatory environmental models and radiological models), a moderate conservatism, transparency, relative simplicity and user friendliness are required. Because the interaction between crops and the environment is complex and regulated by many feedback mechanisms, however, these requirements are difficult to accomplish. The present study makes a step forward regarding the development of a robust model dealing with food contamination after a short-term accidental emission and considers a single crop species, rice (Oryza sativa), one of the most widely used rice species. Old and more recent experimental data regarding the carbon dynamics in rice plants are reviewed, and a well-established crop growth model, ORYZA2000, is used and adapted in order to assess the dynamics of {sup 14}C in rice after a short-term exposure to {sup 14}CO{sub 2}. Here, the model is used to investigate the role of the genotype, management and weather on the concentration of radiocarbon at harvest. (orig.)

  14. 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)

    2012-01-01

    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 14 C 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 14 C 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 14 C 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 14 C, 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

  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

    Energy Technology Data Exchange (ETDEWEB)

    NONE

    2012-06-15

    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 {sup 14}C 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 {sup 14}C 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 {sup 14}C 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 {sup 14}C, 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

  16. Carbon-14 tracer study of polyacrylate polymer in a wastewater plant

    International Nuclear Information System (INIS)

    Martin, J.E.; King, L.W.; Hylko, J.M.

    1990-01-01

    A highly absorbent consumer-product, polyacrylate-polymer material tagged with carbon-14 ( 14 C), was dosed to a standard on-site aerobic wastewater treatment plant which contained a settling chamber, an aeration chamber, and an effluent chamber. Operation of the test plant was essentially the same as that of a control plant even under exaggerated conditions. About 97% of the polymer material was retained in solids deposited in the primary and aeration chambers, and effluent releases were minimal. The use of a 14 C tagging procedure proved to be a successful method for studying the behavior of these complex materials. It may be useful to conduct a further study on retained solids to determine whether microbial decomposition of the polymer material occurs while they remain in typical plants. (author)

  17. Reduction of sources of error and simplification of the Carbon-14 urea breath test

    International Nuclear Information System (INIS)

    Bellon, M.S.

    1997-01-01

    Full text: Carbon-14 urea breath testing is established in the diagnosis of H. pylori infection. The aim of this study was to investigate possible further simplification and identification of error sources in the 14 C urea kit extensively used at the Royal Adelaide Hospital. Thirty six patients with validated H. pylon status were tested with breath samples taken at 10,15, and 20 min. Using the single sample value at 15 min, there was no change in the diagnostic category. Reduction or errors in analysis depends on attention to the following details: Stability of absorption solution, (now > 2 months), compatibility of scintillation cocktail/absorption solution. (with particular regard to photoluminescence and chemiluminescence), reduction in chemical quenching (moisture reduction), understanding counting hardware and relevance, and appropriate response to deviation in quality assurance. With this experience, we are confident of the performance and reliability of the RAPID-14 urea breath test kit now available commercially

  18. An assessment of the inventory of Carbon-14 in the oceans

    International Nuclear Information System (INIS)

    Lassey, K.R.; Manning, M.R.; O'Brien, B.J.

    1987-04-01

    The oceanic inventory for natural 14 C is 19.6x10 29 atoms, an estimate similar to those found by other methods. The 14 C produced from nuclear weapons (1972) is 550x10 26 atoms and 52% was in the oceans. From 1972 to 1985 132x10 26 atoms of bomb 14 C were added. The nuclear power industry produces 0.5x10 26 atoms per year (17% of natural production rate). Most estimates by varying methods indicate an exchange time of carbon from atmosphere to ocean of about seven years or about 22 moles m -2 yr -1 for the surface ocean. The oceanic distribution generally has higher concentrations in low to mid latitudes, and low concentrations in the most southern regions, with the deep ocean retaining levels similar to those before nuclear testing

  19. Study on hydrogen transfer in coal liquefaction by tritium and carbon-14 tracers

    International Nuclear Information System (INIS)

    Nitoh, Osamu; Kabe, Toshiaki; Kabe, Yaeko.

    1985-01-01

    For the analysis of mechanism of hydrogenation and cracking of coal, the liquefaction of Taiheiyo coal using tritium labeled gaseous hydrogen and tritium labeled tetralin with small amounts of carbon-14 labeled naphthalene has been studied. Taiheiyo coal(25g) was thermally decomposed in tetralin or naphthalene solvent(75g) at 400--440 0 C under the initial hydrogen pressure of 5.9MPa for 30min with Ni-Mo-Al 2 O 3 catalyst(0--5g). The reaction mixture in an autoclave was separated by filtration, distillation and solvent extraction. Produced gas, oils and the solvent were analyzed by gas chromatography. The tritium and carbon-14 contents of separated reaction products were measured with a liquid scintilation counter to study the hydrogen transfer mechanism. The distribution of reaction products and the amount of hydrogen transfer from gas or solvent to the products were also determined. In hydrogen donor solvent such as tetralin, the coal liquefaction yield was independent from the catalyst, but the catalyst was effective in hydrocracking of preasphaltene and asphaltene. In naphthalene solvent, the coal liquefaction reaction hardly occured in the absence of the catalyst, because hydrogen transfer from both the solvent and gaseous hydrogen was scarce. Tritium distribution in the reaction products showed that complicated hydrogen exchange reactions between gaseous hydrogen, coal liquids and solvent came out by the presence of coal liquids and catalyst. The very small amounts of carbon-14 transferred to the liquefaction products showed that carbon exchange or transfer between solvent and coal did not take place. (author)

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

    International Nuclear Information System (INIS)

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

    2010-01-01

    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 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 14 C/C ratio, independent of chemical separation procedures. The isotope ratio measurement was specific (owing to the 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 14 C corresponds to 30 fg equivalents. AMS

  1. 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

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

    International Nuclear Information System (INIS)

    Hesboel, R.; Puigdomenech, I.; Evans, S.

    1990-01-01

    The source term, isolation capacity, and long-term radiological exposure of 14 C from the Swedish underground repository for low and intermediate level waste (SFR) is assessed. The prospective amount of 14 C in the repository is assumed to be 5 TBq. Spent ion exchange resins will be the dominant source of 14 C. The pore water in the concrete repository is expected to maintain a pH of >10.5 for a period of at least 10 6 y. The cement matrix of the repository will retain most of the 14 CO 3 2- initially present. Bacterial production of CO 2 and CH 4 from degradation of ion-exchange resins and bitumen may contribute to 14 C release to the biosphere. However, CH 4 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 2.4x10 4 years. A total leakage of 8.4 GBq of 14 C from the repository will cause a total collective dose commitment of 1.1 manSv or 130 manSv TBq -1 . (authors)

  3. A perspective on tritium versus carbon-14: ensuring optimal label selection in pharmaceutical research and development.

    Science.gov (United States)

    Krauser, Joel A

    2013-01-01

    Tritium ((3) H) and carbon-14 ((14) C) labels applied in pharmaceutical research and development each offer their own distinctive advantages and disadvantages coupled with benefits and risks. The advantages of (3) H have a higher specific activity, shorter half-life that allows more manageable waste remediation, lower material costs, and often more direct synthetic routes. The advantages of (14) C offer certain analytical benefits and less potential for label loss. Although (3) H labels offer several advantages, they might be overlooked as a viable option because of the concerns about its drawbacks. A main drawback often challenged is metabolic liability. These drawbacks, in some cases, might be overstated leading to underutilization of a perfectly viable option. As a consequence, label selection may automatically default to (14) C, which is a more conservative approach. To challenge this '(14) C-by-default' approach, pharmaceutical agents with strategically selected (3) H-labeling positions based on non-labeled metabolism data have been successfully implemented and evaluated for (3) H loss. From in-house results, the long term success of projects clearly would benefit from a thorough, objective, and balanced assessment regarding label selection ((3) H or (14) C). This assessment should be based on available project information and scientific knowledge. Important considerations are project applicability (preclinical and clinical phases), synthetic feasibility, costs, and timelines. Copyright © 2013 John Wiley & Sons, Ltd.

  4. Synthesis of 1-(4-methylsulfone-phenyl)-5-(4-fluoro-phenyl)-5-[14C]-1,2,3- triazole and 1-(4-sulfonamide-phenyl)-5-(4-fluoro-phenyl)-5-[14C]-1,2,3- triazole as novel carbon-14 anticonvulsant

    International Nuclear Information System (INIS)

    Saemian, N.; Shirvani, G.; Matloubi, H.

    2006-01-01

    Two 1,2,3-triazole anticonvulsants, 1-(4-methylsulfone-phenyl)-5-(4-fluoro-phenyl)-5-[ 14 C]-1,2,3-triazole and 1-(4-sulfonamide-phenyl)-5-(4- fluoro-phenyl)-5-[ 14 C]-1,2,3-triazole, both labeled with carbon-14 in the 5-position were prepared from para-fluoro-benzonitrile-[cyano- 14 C]. (author)

  5. Carbon-14 isotope effects in the addition of 2,4-dinitrobenzenesulfenyl chloride to styrene-1-14C and styrene-2-14C

    International Nuclear Information System (INIS)

    Kanska, M.; Fry, A.

    1982-01-01

    The carbon-isotope effect reported here represents the first step in a general study of the mechanisms of simple electrophilic addition reactions by isotope effect techniques using the successive labeling approach. The addition of 2,4-dinitrobenzenesulfenyl chloride to styrene was chosen as a ''calibration case'' for the cyclic mechanism. The observed isotope effects at /sup α/C and /sup #betta#/C are fully consistent with the cyclic mechanism and probably inconsistent with the open carbenium ion mechanisms. The values of 12 k/ 14 k indicated in this report are averages (and standard deviations) of values for five different fractions of reaction ranging from 20% to 70% with the calculations being made by all four of the Tong and Yankwich equations for each fraction of reaction. Results indicated that there were no trends in the 12 k/ 14 k values as the fraction of reaction varied, and as can be seen by the low standard deviations, there was good agreement among the values calculated by the four equations. These two facts to indicate that the starting materials were of high chemical and radiochemical purity and that the procedures used in the isotope effect experiments were accurate and properly controlled

  6. 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)

  7. Metabolism of carbon-14 labelled l-tryptophan, l-kynerenine and hydroxy-l-kynerenine in miners with scleroderma

    International Nuclear Information System (INIS)

    Hankes, L.V.; De Bruin, E.; Jansen, C.R.; Voster, L.; Schmaeler, M.

    1977-01-01

    Six South African white miners were studied with the 2-g l-tryptophan load test and tracer doses of L-tryptophan-7a-carbon-14, L-kynurenine-keto-carbon-14 and hydroxy-L-kynerenine-keto-carbon-14. The breath 14 CO 2 and 14 urinary metabolites were measured. When they were compared with a previous study of American women with scleroderma, similar 14 CO 2 and tryptophan metabolite excretion patterns were observed in the data from the miners. The labelled quinolinic acid excretion was more significantly elevated in the South African miners' urine than in the urine of the American women. The data from both studies suggest that some patients with scleroderma have an altered step in the tryptophan metabolic pathway after hydroxy-anthranilic acid. What relationship exists between the induction of pulmonary silicosis and the subsequent development of scleroderma, requires additional human studies

  8. Application of Alkenone 14C-Based chronostratigraphy in carbonate barren sediments on the Peru Margin.

    Science.gov (United States)

    Higginson, M. J.; Altabet, M. A.; Herbert, T. D.

    2003-04-01

    Despite the availability of high-quality sediment cores in key locations, little paleoclimatic information exists for the Peru margin largely because poor carbonate preservation severely restricts the use of traditional carbonate-based proxies for stratigraphy, dating, and paleo-environmental reconstruction. Many sites also include hiatuses produced by the variable influence of undercurrents on sediment accumulation. To overcome these difficulties, we have developed (in collaboration with T. Eglinton, WHOI) a laboratory facility to successfully extract and purify haptophyte-derived alkenones for compound specific 14C AMS dating (modified from OHKOUCHI et al., 2002). This avoids potential problems with dating bulk organic carbon which we assume, even in an upwelling environment as highly productive as the Peru margin, is not a priori solely of marine origin. In a recently collected, mid-Peru Margin core (ODP Leg 201 Site 1228D), comparison of our alkenone 14C dates with bulk sediment organic carbon dates and known stratigraphic markers produces a very well constrained, curvilinear age-depth relationship for at least the last 14 Kyr. A discrete ash layer at Site 1228D with an adjacent alkenone 14C age of 3890 ± 350 yr, is within error identical to the 14C age of a prominent ash layer (3800 ± 50 yr) found west of the large Peruvian El Misti volcano (16^o18'S, 71^o24'W). In summary, these results show that the Peru margin alkenones are autochthonous (i.e. not from an older, distant source) and provide sufficient dating precision to permit, for the first time, high-resolution paleoceanographic studies in this highly important marine province. Based upon this new chronology, synchronous changes in alkenone-derived SST estimates in two of our independently-dated records are the first to record at high-resolution (a) a large LGM-Holocene SST range in the Tropics (up to 7.8 ^oC during brief events in this upwelling location); and (b) sharp coolings (4 ^oC) consistent with

  9. Determination of the carbon content of domestic farm produces to estimate offsite C-14 ingestion dose

    International Nuclear Information System (INIS)

    Jung, Y. G.; Kim, M. J.; Lee, G. B.

    2003-01-01

    The carbon content of grains, leafy and root vegetables, and fruits which the Koreans usually eat were calculated to use in the estimation of offsite C-14 ingestion dose. With the data of food intake per day in the Report on 1998 national health and nutrition survey- dietary intake survey, 5 age-group integrate d intake of the 4 farm produce groups were extracted for food items and the amount. Intake percentage in each food group were taken as food weighing factor for the foods. Carbon content was calculated using protein, fat, and carbohydrate content of the foods, and multiplied by the corresponding food weighing factor to derive the content of the food groups. The calculated carbon content of grains, leafy and root vegetables, and fruits were 39.%, 4.2%, 8.0%, and 5.9% respectively. Grains and fruits were not much different from ODCM for carbon content, but vegetables were higher by 0.7%∼4.5%

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

    International Nuclear Information System (INIS)

    Bird, G.A.

    1996-09-01

    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

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

    Energy Technology Data Exchange (ETDEWEB)

    Bird, G.A. [AECL, Pinawa, MB (Canada). Whiteshell Labs.] [and others

    1996-09-01

    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

  12. Radioactivity measurement of barium carbonate [14C] by liquid scintillation counting

    International Nuclear Information System (INIS)

    Kobayashi, Katsutoshi; Hoizumi, Kiyoshi

    1985-03-01

    Two methods of sample preparation for the measurement of specific activity of BaCO 3 [ 14 C] by external standard method in liquid scintillation counting were studied. BaCO 3 [ 14 C] was decomposed by perchloric acid solution and generated CO 2 [ 14 C] was absorbed by ethylene glycol monomethyl ether solution of monoethanolamine as the method 1 or aqueous sodium hydroxide as the method 2. In order to prepare the sample solution of adequate radioactivity concentration, these carbonate solutions by the methods 1 and 2 were diluted with the suitable organic solvent and distilled water respectively. One tenth millilitre of these sample solutions was added into 10 ml of PPO-toluene scintillator containing 0.1 ml of monoethanolamine in a counting vial and homogeneously dissolved with ethyl alcohol. The results of the radioactivity measurement of BaCO 3 [ 14 C] based on the different method agreed within 5 % and the counting rate was found to be stable for as long as 7 deays or more. Both methods of preparation are suitable for the routine measurement because of their simplicity and feasibility. In the case of method 2, the liquid radioactive waste is almost inorganic solution and recovery in the form of BaCO 3 [ 14 C] is easily performed, so that this method is very advantageous from the view point of the radioactive waste treatement. (author)

  13. Experience of an inter-laboratory exercise for the determination of Carbon-14 in biological samples

    International Nuclear Information System (INIS)

    Baburajan, A.; Rajaram, S.; D'Souza, Renita Shiny; Nayak, Rasmi; Karunakara, N.; Ravi, P.M.; Tripathi, R.M.

    2018-01-01

    Carbon-14 is one of the naturally occurring cosmogenic nuclide with long half life of 5730 y and beta energy, E max : 156 keV produced continuously in the outer atmosphere. It is also produced by the anthropogenic activities like nuclear weapon test, nuclear power plant etc. contributing to the atmospheric inventory. The 14 CO 2 gets incorporated with the plant species during photosynthesis and ultimately reaches to man through food chain. It is important to accurately quantify the level of 14 C in different biological matrices for the computation of radiation dose due to ingestion. There are different methods available for the determination of 14 C in biological samples. The oxidation of the dried sample is one of the methods used for liberating the 14 CO 2 and which in turn re-absorbed using Carbo Sorb and subjected to Liquid scintillation analyses with Permaflour scintillator solution. The paper deals with the quality assurance programme initiated by ESL, Tarapur along with ESL, Kalpakkam and CARER, Mangalore University and share the experience of the inter-laboratory comparison exercise

  14. Application of the dose limitation system to the control of carbon-14 releases from heavy-water-moderated reactors

    International Nuclear Information System (INIS)

    Beninson, D.; Gonzalez, A.J.

    1982-01-01

    Heavy-water-moderated reactors produce substantially more carbon-14 than light-water reactors. Applying the principles of the systems of dose limitation, the paper presents the rationale used for establishing the release limit for effluents containing this nuclide and for the decisions made regarding the effluent treatment in the third nuclear power station in Argentina. Production of carbon-14 in PHWR and the release routes are analysed in the light of the different effluent treatment possibilities. An optimization assessment is presented, taking into account effluent treatment and waste management costs, and the collective effective dose commitment due to the releases. The contribution of present carbon-14 releases to future individual doses is also analysed in the light of an upper bound for the contribution, representing a fraction of the individual dose limits. The paper presents the resulting requirements for the effluent treatment regarding carbon-14 and the corresponding regulatory aspects used in Argentina. (author)

  15. Contribution of deep sourced carbon from hydrocarbon seeps to sedimentary organic carbon: Evidence from Δ14C and δ13C isotopes

    Science.gov (United States)

    Feng, D.; Peckmann, J.; Peng, Y.; Liang, Q.; Roberts, H. H.; Chen, D.

    2017-12-01

    Sulfate-driven anaerobic oxidation of methane (AOM) limits the release of methane from marine sediments and promotes the formation of carbonates close to the seafloor along continental margins. It has been established that hydrocarbon seeps are a source of dissolved inorganic and organic carbon to marine environments. However, questions remain about the contribution of deep sourced carbon from hydrocarbon seeps to the sedimentary organic carbon pool. For a number of hydrocarbon seeps from the South China Sea and the Gulf of Mexico, the portion of modern carbon was determined based on natural radiocarbon abundances (Δ14C) and stable carbon isotope (δ13Corganic carbon) compositions of the non-carbonate fractions extracted from authigenic carbonates. Samples from both areas show a mixing trend between ideal planktonic organic carbon (δ13C = -22‰ VPDB and 90% modern carbon) and the ambient methane. The δ13Corganic carbon values of non-carbonate fractions from three ancient seep deposits (northern Italy, Miocene; western Washington State, USA, Eocene to Oligocene) confirm that the proxy can be used to constrain the record of sulfate-driven AOM through most of Earth history by measuring the δ13C values of organic carbon. This study reveals the potential of using δ13C values of organic carbon to discern seep and non-seep environments. This new approach is particularly promising when authigenic carbonate is not present in ancient sedimentary environments. Acknowledgments: The authors thank BOEM and NOAA for their years' support of the deep-sea dives. Funding was provided by the NSF of China (Grants: 41422602 and 41373085).

  16. Quantitative carbon-14 autoradiography at the cellular level: principles and application for cell kinetic studies. [Review

    Energy Technology Data Exchange (ETDEWEB)

    Doermer, P [Gesellschaft fuer Strahlen- und Umweltforschung m.b.H., Muenchen (Germany, F.R.). Inst. fuer Haematologie

    1981-03-01

    Amounts of radio-labelled substances as low as 10/sup -18/ moles incorporated into individual cells can be measured by utilizing techniques of quantitative autoradiography. The principles and application of quantitative carbon-14 autoradiography are reviewed. Silver grain densities can be counted by automated microphotometry allowing on-line data processing by an interfaced computer. Rate measurements of /sup 14/C-thymidine incorporation into individual cells yield values of the DNA synthesis rate and the DNA synthesis time of a cell compartment can be derived. This is an essential time parameter for the evaluation of kinetic events in proliferating cell populations. This method is applicable to human cells without radiation hazard to man and provides an optimal source of detailed information on the kinetics of normal and diseased human haematopoiesis. Examples of application consist of thalassaemia, malaria infection, iron deficiency anaemia and acute myelogenous leukaemia.

  17. The evolution of carbon-14 and tritium containing gases in a radioactive waste repository

    International Nuclear Information System (INIS)

    Jefferies, N.L.

    1990-04-01

    The principal processes which well lead to the formation of gases in a repository containing low- and intermediate-level radioactive waste have been identified as corrosion, microbiological activity and radiolysis. The largest contribution to gas production is from hydrogen, generated from anaerobic corrosion of metallic components of the waste. Substitution of the active isotopes carbon-14 and hydrogen-3 (tritium) into the bulk gases, H 2 CO 2 and CH 4 may result in a radiological hazard to man. The purpose of this paper is to assess the mechanisms by which C-14 and tritium in solid low- and intermediate-level wastes are partitioned into gases reduced by corrosion and microbial processes. (author)

  18. Carbon-14 based determination of the biogenic fraction of industrial CO(2) emissions - application and validation.

    Science.gov (United States)

    Palstra, S W L; Meijer, H A J

    2010-05-01

    The (14)C method is a very reliable and sensitive method for industrial plants, emission authorities and emission inventories to verify data estimations of biogenic fractions of CO(2) emissions. The applicability of the method is shown for flue gas CO(2) samples that have been sampled in 1-h intervals at a coal- and wood-fired power plant and a waste incineration plant. Biogenic flue gas CO(2) fractions of 5-10% and 48-50% have been measured at the power plant and the waste incineration plant, respectively. The reliability of the method has been proven by comparison of the power plant results with those based on carbon mass input and output data of the power plant. At industrial plants with relatively low biogenic CO(2) fraction (<10%) the results need to be corrected for sampled (14)CO(2) from atmospheric air. Copyright 2009 Elsevier Ltd. All rights reserved.

  19. Quantitative carbon-14 autoradiography at the cellular level: principles and application for cell kinetic studies

    International Nuclear Information System (INIS)

    Doermer, P.

    1981-01-01

    Amounts of radio-labelled substances as low as 10 -18 moles incorporated into individual cells can be measured by utilizing techniques of quantitative autoradiography. The principles and application of quantitative carbon-14 autoradiography are reviewed. Silver grain densities can be counted by automated microphotometry allowing on-line data processing by an interfaced computer. Rate measurements of 14 C-thymidine incorporation into individual cells yield values of the DNA synthesis rate and the DNA synthesis time of a cell compartment can be derived. This is an essential time parameter for the evaluation of kinetic events in proliferating cell populations. This method is applicable to human cells without radiation hazard to man and provides an optimal source of detailed information on the kinetics of normal and diseased human haematopoiesis. Examples of application consist of thalassaemia, malaria infection, iron deficiency anaemia and acute myelogenous leukaemia. (author)

  20. Carbon-14 radiolabelling and tissue distribution evaluation of a potential anti-TB compound.

    Science.gov (United States)

    Sonopo, Molahlehi S; Venter, Kobus; Winks, Susan; Marjanovic-Painter, Biljana; Morgans, Garreth L; Zeevaart, Jan R

    2016-06-15

    This paper describes a five-step synthesis of a carbon-14-labelled pyrazole compound (11). A total of 2.96 MBq of 11 was obtained with the specific activity of 2242.4 MBq/mmol. The radiochemical purity was >99%, and the overall radiochemical yield was 60% based on the [(14) C6 ] 4-bromoaniline starting material. Biodistribution results showed that the radiotracer (administrated orally) has a high accumulation in the small intestine, large intestine and liver of both non-infected and tuberculosis (TB)-infected mice. Therefore, this suggests that compound 11 undergoes hepatobiliary clearance. The compound under investigation has been found to be slowly released from the liver between 2 and 8 h. The study revealed that 11 has no affinity for TB cells. Copyright © 2016 John Wiley & Sons, Ltd.

  1. Biogenesis of tritiated and carbon-14 methane from low-level radioactive waste

    International Nuclear Information System (INIS)

    Francis, A.J.; Dobbs, S.; Doering, R.F.

    1980-01-01

    Methane bacteria were detected in leachate samples collected from commercial low-level radioactive waste disposal sites. Significant amounts of tritiated and carbon-14 methane were generated by a mixed methanogenic culture from a leachate sample collected from the low-level radioactive waste disposal site, Maxey Flats, KY. Tritiated methane was produced by methane bacteria from synthetic media containing 2 mCi of tritium as tritiated water or tritiated acetate, and the level of tritium added to the medium had no effect on methanogenesis. Under anaerobic conditions the organic compounds containing 14 C and 3 H activity and tritiated water in the waste are metabolized by microorganisms and they produce radioactive gases which escape into the environment from the disposal sites. 4 figures, 3 tables

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

    International Nuclear Information System (INIS)

    Fischer, E.; Mueller, H.

    1980-01-01

    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 14 C- and of the 3 H-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 3 H-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.) [de

  3. Use of the small gas proportional counters for the carbon-14 measurement of very small samples

    International Nuclear Information System (INIS)

    Sayre, E.V.; Harbottle, G.; Stoenner, R.W.; Otlet, R.L.; Evans, G.V.

    1981-01-01

    Two recent developments are: the first is the mass-spectrometric separation of 14 C and 12 C ions, followed by counting of the 14 C, while the second is the extension of conventional proportional counter operation, using CO 2 as counting gas, to very small counters and samples. Although the second method is slow (months of counting time are required for 10 mg of carbon) it does not require operator intervention and many samples may be counted simultaneously. Also, it costs only a fraction of the capital expense of an accelerator installation. The development, construction and operation of suitable small counters are described, and results of three actual dating studies involving milligram scale carbon samples will be given. None of these could have been carried out if conventional, gram-sized samples had been needed. New installations, based on the use of these counters, are under construction or in the planning stages. These are located at Brookhaven Laboratory, the National Bureau of Standards (USA) and Harwell (UK). The Harwell installation, which is in advanced stages of construction, will be described in outline. The main significance of the small-counter method is, that although it will not suffice to measure the smallest (much less than 10 mg) or oldest samples, it will permit existing radiocarbon laboratories to extend their capability considerably, in the direction of smaller samples, at modest expense

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

    International Nuclear Information System (INIS)

    Lu, Ning; Ross, B.

    1993-01-01

    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

  5. 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)

  6. Kinetics of extracellular release of 14C-labelled organic carbon by submerged macrophytes

    International Nuclear Information System (INIS)

    Soendergaard, M.

    1981-01-01

    The release of extracellular organic carbon (EOC) by six submerged freswater macrophytes was measured in time course studies with a 14 C-technique. Incubation in light in an open water-flow system made it possible to assay the time courses of 14 C-fixation and the simultaneous release of labelled EOC. Heterotrophic utilization of the released products by epiphytic communities was measured. Two patterns of release kinetics were found: (1) Constant rates of release occurred during the incubations, (2) The rates still increased after 24 h of incubation. During the first hours of incubation the rates of release increased in all species. Elodea reached constant rates after 2-4 h and Littorella and Ceratophyllum demersum after about 20 h. In the experiments with C. submersum and Nitella the rates of release increased almost linearly during the entire incubation period. The kinetics of release were in agreement with the molecular weight distribution of the dissolved EOC measured with gel chromatography. Low molecular weight products ( 10000 Daltons) dominated the dissolved EOC released by C. submersum and Nitella. A large fraction (18-60%) of the total EOC could be recovered on filters with a pore size of 0.2 μm. This particulate fraction probably represents some abiotic removal. The quantities of relase were low in all species and did not exceed 0.9% of the photosynthetic carbon fixation. Heterotrophic uptake by the epiphytic communities was less than 10% of the EOC released. The results emphasize that the 14 C-labelling of extracellular products is a time dependent process. (author)

  7. Revision of Fontes & Garnier's model for the initial 14C content of dissolved inorganic carbon used in groundwater dating

    Science.gov (United States)

    Han, Liang-Feng; Plummer, Niel

    2013-01-01

    The widely applied model for groundwater dating using 14C proposed by Fontes and Garnier (F&G) (Fontes and Garnier, 1979) estimates the initial 14C content in waters from carbonate-rock aquifers affected by isotopic exchange. Usually, the model of F&G is applied in one of two ways: (1) using a single 13C fractionation factor of gaseous CO2 with respect to a solid carbonate mineral, εg/s, regardless of whether the carbon isotopic exchange is controlled by soil CO2 in the unsaturated zone, or by solid carbonate mineral in the saturated zone; or (2) using different fractionation factors if the exchange process is dominated by soil CO2 gas as opposed to solid carbonate mineral (typically calcite). An analysis of the F&G model shows an inadequate conceptualization, resulting in underestimation of the initial 14C values (14C0) for groundwater systems that have undergone isotopic exchange. The degree to which the 14C0 is underestimated increases with the extent of isotopic exchange. Examples show that in extreme cases, the error in calculated adjusted initial 14C values can be more than 20% modern carbon (pmc). A model is derived that revises the mass balance method of F&G by using a modified model conceptualization. The derivation yields a “global” model both for carbon isotopic exchange dominated by gaseous CO2 in the unsaturated zone, and for carbon isotopic exchange dominated by solid carbonate mineral in the saturated zone. However, the revised model requires different parameters for exchange dominated by gaseous CO2 as opposed to exchange dominated by solid carbonate minerals. The revised model for exchange dominated by gaseous CO2 is shown to be identical to the model of Mook (Mook, 1976). For groundwater systems where exchange occurs both in the unsaturated zone and saturated zone, the revised model can still be used; however, 14C0 will be slightly underestimated. Finally, in carbonate systems undergoing complex geochemical reactions, such as oxidation of

  8. The synthesis of SL-75.212 (Betaxolol) labelled with carbon 14: 1-[4-(2-cyclopropyl methoxyethyl-[1-14C]) phenoxy]-3-isopropyl amino-2-propanol

    International Nuclear Information System (INIS)

    Aubert, F.; Beaucourt, J.P.; Pichat, L.

    1982-01-01

    Carbonation with 14 CO 2 of the Grigard reagent 1 gave 4-benzyloxy [carboxyl- 14 C] benzoic acid: 2 (87 % yield). 2 was successively treated in diethyl ether solution with diazomethane and lithium aluminium hydride giving rise to [7- 14 C] 4 benzyloxybenzyl alcohol 4 (82 % yield). Alcohol 4 was transformed into the corresponding chloride 5 when exposed to thionylchloride in ether. 5 was condensed with NaCN in DMF to give the nitrile 6 which was hydrolysed into the acid 7 isolated in a 75 % overall yield from Ba 14 CO 3 . 7 gave the alcohol 9 by successive treatments with diazomethane and LiAlH 4 in ether. 9 with NaH gave the corresponding alkoxide which when condensed with bromomethylcyclopropane gave the ether 10 purified by silicagel column chromatography and isolated with an overall yield of 71 % from Ba 14 CO 3 . Hydrogenolysis of 10 gave the phenol 11. The epoxide 12 was secured by condensation with epichlorhydrin in presence of NaOH. After purification by silicagel column chromatography 10 was opened with isopropylamine leading to the target compound BETAXOLOL 13 isolated as the hydrochloride. After extensive purification by Sephadex G-10 column chromatography, SL 75.212 [ethyl-1- 14 C] was obtained in an overall yield of 26 % from barium [ 14 C] carbonate and a radiochemical purity better than 99 % (specific activity 57 mCi/mole). (author)

  9. A study of the carbon dynamics of Japanese grassland and forest using 14C and 13C

    International Nuclear Information System (INIS)

    Katsuno, Kazumi; Miyairi, Yosuke; Tamura, Kenji; Matsuzaki, Hiroyuki; Fukuda, Kenji

    2010-01-01

    We quantified the carbon contents of grassland and forest soil using conventional methods and studied the changes in their dynamics by measuring δ 13 C and Δ 14 C. Soil samples were taken from a neighboring Miscanthus sinensis grassland and Pinus densiflora forest in central Japan. Both had been maintained as grassland until the 1960s, when the latter was abandoned and became a pine forest by natural succession. The soil carbon content of the forest was much lower than that of the grassland, implying that the soil carbon decreased as the grassland became forest. The δ 13 C values were very similar in the grassland and forest, at approximately -20 per mille , suggesting that M. sinensis (a C4 plant) contributed to carbon storage, whereas there was little carbon accumulation from P. densiflora (a C3 plant) in forest soil. The Δ 14 C values and calculated soil carbon mean residence time (MRT) showed that the soil carbon in the upper A horizon was older, and that in the lower A horizon was younger in forest than in grassland. From these results, we conclude that young, fast-MRT soil carbon is decomposed in the upper A horizon, and old, stable soil carbon was decomposed in the lower A horizon after the pine invasion.

  10. Hofmann elimination of p-nitrophenylethyl-1-C-14-trimethylammonium bromide: a carbon-14 isotope effect study (Preprint no. AR-24)

    International Nuclear Information System (INIS)

    Ramamurthy, T.V.; Fry, Arthur

    1991-01-01

    The alpha carbon isotope effects in the Hofmann elimination of p-nitrophenylethyl-1-C-14-trimethylammonium bromide compound have been measured under changing buffer concentrations with a view to correlate mechanistic change. Since there are alpha-carbon isotope effects and the effects are small it is quite likely that the reaction is of the ElcB type, predominately irreversible, with the incursion of slightly increasing fractions of reaction by the reversible mechanism as the buffer concentration is increased. (author). 4 refs., 2 tab

  11. Seasonal dynamics of permafrost carbon emissions: A passive, quasi-continuous 14CO2 sampler

    Science.gov (United States)

    Pedron, S.; Xu, X.; Walker, J. C.; Welker, J. M.; Klein, E. S.; Euskirchen, E. S.; Czimczik, C. I.

    2017-12-01

    Millennia of carbon (C) fixation by tundra vegetation, coupled with low rates of C mineralization by soil microorganisms and preservation in permafrost, have allowed Arctic soils to accumulate vast quantities of organic C (1672 Pg C total). Today, the Arctic is rapidly warming (0.48oC decade-1) and widespread degradation of permafrost may subject permafrost C to microbial mineralization and fluxes to the atmosphere, accelerating climate change. Loss of permafrost C can be quantified in situ by measuring the radiocarbon (14C) content of soil and ecosystem respiration, because permafrost C is older (depleted in 14C) than current plant products and soil C cycling operates on timescales of years to centuries. Here, we use 14C analysis of CO2 respired from graminoid tundra in Arctic Alaska to 1) apportion how plant and microbial respiration contribute to ecosystem respiration in spring, summer, and fall, and 2) elucidate the C sources of microbial respiration throughout the year. We used a novel, passive sampling system, capable of trapping diffusive CO2 throughout the active layer of tussock sedge tundra (n=4, from mineral soil to air) over periods of 2 days to 3 weeks in June 2017. CO2 was collected into various sizes of canisters, ranging from 0.5-32 L, and analyzed for its 14C content at UC Irvine's KCCAMS laboratory. To evaluate the system's efficiency, and quantify the temporal and spatial variability of ecosystem respiration sources, we co-deployed 3 Vaisala Carbocap [CO2] and temperature probes, and traditional chambers (n=6) and gas wells (n=10) for sampling of ecosystem- and soil-respired 14CO2 over 15 min-24 hours. A comparison of traditional methods with our new sampler indicates that the system accurately sampled the expected [CO2] depth gradient. The CO2 sampling rate was positively correlated to soil [CO2] (R2=0.963), equivalent to 1.4*10-3±1.6*10-3 mg C/L/month/ppm (n=8). Gas well and probe concentrations were of the same order of magnitude on the same

  12. Carbonates in leaching reactions in context of {sup 14}C dating

    Energy Technology Data Exchange (ETDEWEB)

    Michalska, Danuta, E-mail: danamich@amu.edu.pl [Institute of Geology, Faculty of Geographical and Geological Sciences, Adam Mickiewicz University, ul. Makow Polnych 16, 61-606 Poznan (Poland); Czernik, Justyna, E-mail: justyna.czernik@gmail.com [Poznań Radiocarbon Laboratory, ul. Rubież 46, 61-612 Poznań (Poland)

    2015-10-15

    Lime mortars as a mixture of binder and aggregate may contain carbon of various origins. If the mortars are made of totally burnt lime, radiocarbon dating of binder yields the real age of building construction. The presence of carbonaceous aggregate has a significant influence on the {sup 14}C measurements results and depending on the type of aggregate and fraction they may cause overaging. Another problem, especially in case of hydraulic mortars that continue to be chemically active for a very long time, is the recrystallization usually connected with rejuvenation of the results but also, depending on local geological structures, with so called reservoir effect yielding apparent ages. An attempt in separating the binder from other carbonaceous components successfully was made for samples from Israel by Nawrocka-Michalska et al. (2007). The same preparation procedure, after taking into account the petrographic composition, was used for samples coming from Poland, Nawrocka et al. (2009). To verify the procedure used previously for non-hydraulic samples determination an experimental tests on carbonaceous mortars with crushed bricks from Novae in Bulgaria were made. Additionally, to identify different carbonaceous structures and their morphology, a cathodoluminescence and scanning electron microscope with electron dispersive spectrometer were applied. The crushed bricks and brick dust used in mortars production process have been interpreted as an alternative use to other pozzolanic materials. The reaction between lime and pozzolanic additives take place easily and affects the rate and course of carbonates decomposition in orthophosphric acid, during the samples pretreatment for dating. The composition of the Bulgarian samples together with influence of climate conditions on mortar carbonates do not allow for making straightforward conclusions in chronology context, but gives some new guidelines in terms of hydraulic mortars application for dating. This work has mainly

  13. Carbonates in leaching reactions in context of "1"4C dating

    International Nuclear Information System (INIS)

    Michalska, Danuta; Czernik, Justyna

    2015-01-01

    Lime mortars as a mixture of binder and aggregate may contain carbon of various origins. If the mortars are made of totally burnt lime, radiocarbon dating of binder yields the real age of building construction. The presence of carbonaceous aggregate has a significant influence on the "1"4C measurements results and depending on the type of aggregate and fraction they may cause overaging. Another problem, especially in case of hydraulic mortars that continue to be chemically active for a very long time, is the recrystallization usually connected with rejuvenation of the results but also, depending on local geological structures, with so called reservoir effect yielding apparent ages. An attempt in separating the binder from other carbonaceous components successfully was made for samples from Israel by Nawrocka-Michalska et al. (2007). The same preparation procedure, after taking into account the petrographic composition, was used for samples coming from Poland, Nawrocka et al. (2009). To verify the procedure used previously for non-hydraulic samples determination an experimental tests on carbonaceous mortars with crushed bricks from Novae in Bulgaria were made. Additionally, to identify different carbonaceous structures and their morphology, a cathodoluminescence and scanning electron microscope with electron dispersive spectrometer were applied. The crushed bricks and brick dust used in mortars production process have been interpreted as an alternative use to other pozzolanic materials. The reaction between lime and pozzolanic additives take place easily and affects the rate and course of carbonates decomposition in orthophosphric acid, during the samples pretreatment for dating. The composition of the Bulgarian samples together with influence of climate conditions on mortar carbonates do not allow for making straightforward conclusions in chronology context, but gives some new guidelines in terms of hydraulic mortars application for dating. This work has mainly

  14. Carbon-14 Specific Activity Model Validation for Biota in Wetland Environments

    International Nuclear Information System (INIS)

    Yankovich, T.L.; Sharp, K.J.; Benz, M.L.; Carr, J.; Killey, R.W.D.

    2008-01-01

    In many cases, contaminants, such as radionuclides, can show highly localized spatial distributions in natural systems. Therefore, a key question for environmental assessment and monitoring becomes, how can these localized distributions of contaminants in the environment lead to organism exposure, and ultimately, the potential for effects to receptor biota? To address this question, an important first step is to conduct field surveys at sites of interest to map out the spatial distribution and extent of contaminants in areas that are being occupied and utilized by resident receptor biota. Work can then be conducted to establish predictive relationships between contaminant concentrations in biota tissues and those in environmental media with which biota interact, to gain an understanding of how representative ambient contaminant concentrations are of biota exposure. The objectives of this study were: - To conduct a field survey in a wetland ecosystem to characterize the spatial distribution of carbon- 14 ( 14 C), a radionuclide with dynamics in natural systems that can be described using a specific activity model; and - To determine whether 14 C concentrations in environmental media reflect those measured in tissues of resident flora and fauna. A detailed field campaign was carried out in summer 2001 to characterize the spatial distribution and areal coverage of 14 C in Duke Swamp, a wetland ecosystem on Atomic Energy of Canada Limited (AECL)'s Chalk River Laboratories (CRL) site that receives 14 C through releases from an up-gradient Waste Management Area (WMA), primarily through groundwater influx. Sampling of surface vegetation (dominantly comprised of Sphagnum moss) was conducted at a total of 69 locations, with complementary sampling of air, soil, fungi, aerial insects, ground-dwelling insects, amphibians, small mammals and snakes being carried out at a subset of five locations with varying 14 C concentrations. Concentrations of 14 C in resident Duke Swamp

  15. Carbon-14, tritium, stable isotope and chemical measurements on thermal waters from the Tauranga region

    International Nuclear Information System (INIS)

    Stewart, M.K.; McGill, R.C.; Taylor, C.B.; Whitehead, N.E.; Downes, C.J.

    1984-03-01

    The chemical compositions of groundwater from the Tauranga region are affected to varying degrees by reducing conditions due to buried organic matter. The levels of some dissolved constituents are also affected by mixing with sea water contained within the rocks and by rock-water interaction. Dissolved gas compositions range from oxygen-bearing to methane-bearing reflecting the varying redox conditions. Excess air may be present but further experiments are necessary to confirm this. Apparent ages deduced from carbon-14 measurements (corrected using 12C dilution and 13C fractionation methods) range from 2-25,000 years, suggesting that some of the waters were recharged during late Pleistocene or early Holocene time. ΔD and Δ18 O values of the oldest waters are slightly more negative than those of younger samples; this may indicate recharge during a cooler climate, in agreement with the 14C ages. Very low but significantly non-zero tritium contents (TR=(0.007-0.059)+-0.007) were measured using the high tritium-enrichment facilities at INS and the very low-background counters at the University of Bern. The tritium is thought to derive from contamination or nuclear reactions in the aquifer rocks rather than from recharge water

  16. Use of radio-active carbon (/sup 14/C) for measuring organic production in the sea

    Energy Technology Data Exchange (ETDEWEB)

    Nielsen, E S

    1952-01-01

    A method for measuring the photosynthesis of plankton algae in a water sample by means of assimilated /sup 14/C is described. It is shown that the assimilation of /sup 14/C in organic matter otherwise than by photosynthesis is of quite insignificant importance. An account is given of the isotope effect in photosynthesis. Two different methods for the measurement of production of matter per surface unit are described. In the first method samples of water are taken from the various depths and transferred to bottles with glass stoppers. After addition of /sup 14/C, the bottles are suspended at the depths from which the samples were taken, and left there from noon to sunset, for instance. In the other method the bottles are placed in a water-bath which is illuminated by a definite light intensity. The penetration of light in the sea is determined at the same time. The production of matter per surface unit is calculated by means of a formula involving the determination of the depth at which 1 per cent of the total amount of green and blue light occurs, and measurement of the intensities of assimilation in water-bath. The formula, which applies to the tropics, has been derived by comparing the results from all tropical stations, at which observations by the two methods were made simultaneously. The values found for production of matter on a section across the Indian Ocean are recorded. The net production of matter for all sea regions on the globe is estimated at about 1.5 x 10/sup +10/ tons of carbon per year, which is slightly less than the amount produced on land, and the hitherto accepted figures for the production of matter in the sea have proved to be greatly exaggerated.

  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)

    Hwang, B.K.; Ibenthal, W.-D.; Heitefuss, R.

    1986-01-01

    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 14 CO 2 assimilation, distribution of 14 C, and 14 C-carbonate uptake in different organs of healthy and infected plants. The reduction of 14 CO 2 assimilation in infected plants at the first and fourth leaf stages was greater in Peruvian than in Asse. In Peruvian, the 14 C 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 14 CO 2 assimilation in noninfected fourth leaves of Asse less than that of Peruvian, but the flow of 14 C 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 14 C-carbonate by seedling roots, the reduction being greater in Peruvian than Asse. A greater proportion of the 14 C 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. 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

    International Nuclear Information System (INIS)

    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 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 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 2 fertilization and impose a constraint on the ultimate total carbon mass in the biosphere

  19. 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. Copyright © 2015 John Wiley & Sons, Ltd.

  20. 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).

  1. Systematical investigations of the emission of carbon 14 from a TRIGA-Mark-II reactor - methods and results

    International Nuclear Information System (INIS)

    Pfeiffer, K.J.

    1981-01-01

    Almost no information is available about the extent of the carbon-14 releases from a research reactor. For this reason this report is dealing with the emission of C-14 from the Vienna TRIGA-Mark-II reactor. In addition the resulting radiation exposure is estimated. Due to the low activity concentrations of C-14 in research reactor effluents special requirements are necessary for sampling and measuring. A technique providing both sufficient lower limit of detection and little effort of sample preparation was developed. Carbon dioxide was trapped by bubbling air taken from the stack through washing bottles containing an aqueous solution of sodium hydroxide. After sampling a precipitate of CaCO 3 was formed and about 8 g of calcium carbonate were counted as a gel suspension by liquid scintillation counting. The formation of the gel was provided by mixing water with a scintillation cocktail originally developed for uptake of high quantities of aqueous solutions. The resulting lower limit of detection was about 50 Bq/kg carbon being equivalent to 9mBq/m 3 air. Concluding the measurements, which were carried out by weekly counting and a period of some 14 months, a normalized release rate of about 280 Bq (7, 1μCi) was found. This release rate is somewhat higher than the reported values for power reactors, because the main activity is produced by activation of air in experimental equipments. (author)

  2. Carbon-14 dating of a mummy from 'Caverna da Babilonia', Rio Novo Country, south of Minas Gerais (MG, Brazil)

    International Nuclear Information System (INIS)

    Beltrao, M. da C.M.C.; Danon, J.; Poupeau, G.

    1985-01-01

    The vegetable fibers of a cloth wrapping a mummy of a woman, found in 'Caverna da Babilonia' (MG, Brazil), were dated with carbon-14. There is strong evidence that it is a pre-colombian mummym since the age of the sample is 600 + - 80 years (1σ). (C.L.B.) [pt

  3. [Quantifying rice (Oryza sativa L.) photo-assimilated carbon input into soil organic carbon pools following continuous 14C labeling].

    Science.gov (United States)

    Nie, San-An; Zhou, Ping; Ge, Ti-Da; Tong, Cheng-Li; Xiao, He-Ai; Wu, Jin-Shui; Zhang, Yang-Zhu

    2012-04-01

    The microcosm experiment was carried out to quantify the input and distribution of photo-assimilated C into soil C pools by using a 14C continuous labeling technique. Destructive samplings of rice (Oryza sativa) were conducted after labeling for 80 days. The allocation of 14C-labeled photosynthates in plants and soil C pools such as dissolved organic C (DOC) and microbial biomass C (MBC) in rice-planted soil were examined over the 14C labeling span. The amounts of rice shoot and root biomass C was ranged from 1.86 to 5.60 g x pot(-1), 0.46 to 0.78 g x pot(-1) in different tested paddy soils after labeling for 80 days, respectively. The amount of 14C in the soil organic C (14C-SOC) was also dependent on the soils, ranged from 114.3 to 348.2 mg x kg(-1), accounting for 5.09% to 6.62% of the rice biomass 14C, respectively. The amounts of 14C in the dissolved organic C (14C-DOC) and in the microbial biomass C(14C-MBC), as proportions of 14C-SOC, were 2.21%-3.54% and 9.72% -17.2%, respectively. The 14C-DOC, 14C-MBC, and 14C-SOC as proportions of total DOC, MBC, and SOC, respectively, were 6.72% -14.64%, 1.70% -7.67%, and 0.73% -1.99%, respectively. Moreover, the distribution and transformation of root-derived C had a greater influence on the dynamics of DOC and MBC than on the dynamics of SOC. Further studies are required to ascertain the functional significance of soil microorganisms (such as C-sequestering bacteria and photosynthetic bacteria) in the paddy system.

  4. 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.; van Dongen, Bart E.; Semiletov, Igor P.; Dudarev, Oleg V.; Yunker, Mark B.; Macdonald, Robie W.; Wacker, Lukas; Montluçon, Daniel B.; Eglinton, Timothy I.

    2015-11-01

    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.

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

    International Nuclear Information System (INIS)

    Fujio, Shin'ichirou

    2005-01-01

    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)

  6. A study for the fabulously of introducing an acceleration mass spectrometer facility (ABMs) for carbon-14 applications

    International Nuclear Information System (INIS)

    Aly, A.I.M.; Comsan, N.; Sadek, M.

    2004-01-01

    In this work a study was conducted to show the importance and feasibility of introducing an accelerating mass spectrometer facility for carbon-14 analysis in the environmental levels. The different applications of Carbon-14 (e.g. dating and identification of food additives of synthetic origin) are discussed. There are two methods for C- 14 measurements, beta decay counting and accelerator mass spectrometry (AMS). The beta decay method requires gram quantities of the sample carbon, compared to few milligram quantities in case of AMS method. The Central Lab. for Environmental Isotope Hydrology of the National Center for Nuclear Safety and Radiation Control has a Carbon-14 analysis facility based on beta decay counting using a liquid scintillation counter after sample preparation in the form of benzene through rather complicated chemical conversion steps. This strongly limits the capacity of the laboratory to about 100-150 samples per year. Also, the amount of sample required limits our expansion for some very important applications like dating of archaeological small samples and especially old bone samples which normally have a low concentration of organic compounds. These applications are only possible by using the AMS method. For some applications only AMS could be used e.g measuring C-14 in atmospheric gases such as methane and carbon dioxide is virtually impossible using decay counting but quite feasible with AMS. The importance of purchasing an AMS facility or upgrading the existing accelerator is discussed in view of the shortage of such a facility in Africa and the Middle East. Acquiring an AMS in Egypt will make it possible to accurately date the Egyptian antiquities and to act as a regional laboratory and to enter into new applications where the amount of sample is limiting

  7. In situ synthesis of N and Cu functionalized mesoporous FDU-14 resins and carbons for electrochemical hydrogen storage

    Energy Technology Data Exchange (ETDEWEB)

    Kong, AiGuo; Wang, WenJuan; Yang, Fan; Ding, HanMing; Shan, YongKui [Department of Chemistry, East China Normal University, ShangHai 200062 (China)

    2010-07-15

    N and Cu cooperatively functionalized mesoporous resin and carbon materials with bicontinuous cubic structure (FDU-14) were obtained by a novel synthesis method. In this method, block copolymers were used as the templates as well as the precursors for the preparation of these modifying mesoporous materials. The CuC{sub 2}O{sub 4} in the channels of mesoporous FDU-14 resins was gotten by in situ oxidation of the templates in a catalytic redox system containing Cu{sup 2+}, Al{sup 3+}, NO{sub 3}{sup -}, PO{sub 4}{sup 3-}, SO{sub 4}{sup 2-} ions. Simultaneously, the phenol-formaldehyde resin frameworks were in situ functionalized by the amine group resulting from the reduction of NO{sub 3}{sup -}, leading to the formation of N and CuC{sub 2}O{sub 4} modified mesoporous FDU-14 resin materials. Its pyrolysis at the different temperatures resulted in the production of N and Cu cooperatively functionalized mesoporous FDU-14 resin and carbon materials. The structure and composition of these materials were characterized by the X-ray power diffraction, transmission electron microscopy, N{sub 2} adsorption-desorption analysis, X-ray photoelectron spectroscopy, infrared spectroscopy, thermogravimetry analysis, and inductive coupled plasma emission spectroscopy. The electrochemical measurement indicated that N and Cu cooperatively functionalized mesoporous FDU-14 carbon materials possessed the enhanced electrochemical hydrogen storage performance. (author)

  8. Carbon-14 in the biosphere: Modeling and supporting research for the Canadian Nuclear Fuel Waste Management program

    International Nuclear Information System (INIS)

    Sheppard, S.C.; Amiro, B.D.; Sheppard, M.I.; Stephenson, M.; Zach, R.; Bird, G.A.

    1994-01-01

    Carbon-14 stands apart from most of the radionuclides present in nuclear fuel waste for several reasons. It has a relatively long radiological half-life and low retardation by granitic geological media so that 14 C is superceded only by 36 Cl and 129 I in potential release to the biosphere from unprocessed used fuel. In the biosphere, its importance continues because it is readily incorporated into the carbon compounds of life. Much of the behavior of 14 C in the biosphere can be conceptualized as isotopic exchange, where the 14 C mixes with 12 C from the biosphere. However, because of lack of data, the authors model the behavior of 14 C only partly as isotopic exchange, with most of the calculations relying on compartment transfer models. The authors experimental work has shown that soil-to-plant transfer may be dominated by the soil-atmosphere-plant pathway. Gaseous loss of 14 C from soils and lakes is significant. However, recalcitrant forms may persist in soils and sediments for long time periods. The impact of these forms is expected to be relatively low because their bioavailability is correspondingly low. Future research should be directed to support full modeling of 14 C as a series of isotopic exchange processes

  9. Carbon transfer between 2 1/4 Cr 1 Mo alloy and austenitic steels (experiments in anisothermal loops)

    International Nuclear Information System (INIS)

    Baque, P.; Besson, M.; Champeix, L.; Donati, J.R.; Oberlin, C.; Saint-Paul, P.

    1976-01-01

    Studies on carbon transfer between the ferritic steel 2 1/4 Cr 1 Mo and the austenitic steels 316L and 321H have shown that there is not any measurable carbon transfer in the operating conditions of the secondary circuit of PHENIX (475 deg C was the maximal temperature of the 2 1/4 Cr 1 Mo steel). A significant carbon transfer has been observed between the ferritic steel and the 316L steel when the 321H was replaced by the 2 1/4 Cr 1 Mo steel in the same thermohydraulic conditions (the ferritic steel was then used up to 545 deg C). This experiment has demonstrated the importance of the temperature and the initial carbon content of the ferritic steel as parameters in the decarburization process. It appears that decarburization may not be sensitive to the thermohydraulic conditions at least in the range investigated in those experiments. In the other hand the 316L steel is observed to have been carburized, the degree of carburization remaining appreciably constant and independent on the temperature between 400 deg C and 550 deg C [fr

  10. Validation of a simplified carbon-14-urea breath test for routine use for detecting Helicobacter pylori noninvasively

    International Nuclear Information System (INIS)

    Henze, E.; Malfertheiner, P.; Clausen, M.; Burkhardt, H.; Adam, W.E.

    1990-01-01

    A carbon-14 ( 14 C) urea breath test for detecting Helicobacter pylori with multiple breath sampling was developed. Carbon-14-urea (110 kBq) administered orally to 18 normal subjects and to 82 patients with Helicobacter infection. The exhaled 14 C-labeled CO 2 was trapped at 10-min intervals for 90 min. The total 14 C activity exhaled over 90 min was integrated and expressed in %activity of the total dose given. In normals, a mean of 0.59% +/- 0.24% was measured, resulting in an upper limit of normal of 1.07%. In 82 patients, a sensitivity of 90.2%, a specificity of 83.8%, and a positive predictive value of 90.2% was found. The single probes at intervals of 40-60 min correlated best with the integrated result, with r ranging from 0.986 to 0.990. The test's diagnostic accuracy did not change at all when reevaluated with the 40-, 50-, or 60-min sample data alone. Thus, the 14 C-urea breath test can be applied routinely as a noninvasive, low-cost and one-sample test with high diagnostic accuracy in detecting Helicobacter pylori colonization

  11. Evaluation of carbon-14 (C14) levels of terrestrial and marine food products of the environment of the site of Cogema La Hague

    International Nuclear Information System (INIS)

    2006-04-01

    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.)

  12. Response of a carbon-walled proportional counter to 14 MeV neutrons

    International Nuclear Information System (INIS)

    Lewis, K.D.

    1982-01-01

    The response of a carbon-walled spherical proportional counter filled with a methane-based tissue-equivalent gas mixture at low pressure and irradiated with 14 MeV neutrons is first measured experimentally and is then calculated theoretically by using an analytical model. The model, called the CISS model, is derived from a consideration of four basic modes of interaction of charged particles generated in neutron-nucleus reactions with the spherical cavity of the detector. Since several quantities which have application in neutron dosimetry, radiation protection, and radiation biology make direct use of such spectra, it is desirable to have the ability to theoretically predict what is expected experimentally. Thus, a comparison between the two response curves is made. The discrepancy between them is investigated by considering several physical phenomena occurring within the detector wall which tend to distort the experimental response curve. In particular, the C(n,n',3α) reaction occurring in the detector wall gives rise to multiple events, originating from a single neutron interaction in the wall simultaneously strike the detector cavity, and are recorded as a single larger event in an experimental spectra. In the analytic model, the simultaneous entry of two charged particles into the cavity is scored as two separate smaller events, uncorrelated in their production. In this work, an effort is made to modify the analytic model prediction of the response curve by correcting for the multiple events which occur. Finally, the CISS model is used to compute mass stopping power corrections for this inhomogeneous detector

  13. Synthesis and solubility measurement in supercritical carbon dioxide of two solid derivatives of 2-methylnaphthalene-1,4-dione (menadione): 2-(Benzylamino)-3-methylnaphthalene-1,4-dione and 3-(phenethylamino)-2-methylnaphthalene-1,4-dione

    International Nuclear Information System (INIS)

    Zacconi, Flavia C.; Nuñez, Olga N.; Cabrera, Adolfo L.; Valenzuela, Loreto M.

    2016-01-01

    Highlights: • Two menadione derivatives were synthesized, purified and characterized. • Solubility of menadione derivatives in SC-CO 2 was measured at T < 333 K, p < 28 MPa. • Thermodynamic consistency of solubility data measured was evaluated. • Solubility data was correlated in terms of temperature and CO 2 density. - Abstract: Synthesis of two solid derivatives of vitamin K 3 (2-methylnaphthalene-1,4-dione or menadione), 2-(benzylamino)-3-methylnaphthalene-1,4-dione and 3-(phenethylamino)-2-methylnaphthalene-1,4-dione was completed using a 1,4 Michael addition reaction at 323 K in an inert atmosphere, with reaction yields of 62% mol·mol −1 and 71% mol·mol −1 , respectively, and a purity grade of 98% mol·mol −1 for each component. Isothermal solubility (mole fraction) of each solid derivative in supercritical carbon dioxide was performed using an analytic-recirculation methodology, with direct determination of the molar composition of the carbon dioxide-rich phase by using high performance liquid chromatography, at temperatures of (313, 323 and 333) K and pressures from (8–28) MPa. Results indicated that the range of measured solubilities were from (59 × 10 −6 to 368 × 10 −6 ) mol·mol −1 for solid 2-(benzylamino)-3-methylnaphthalene-1,4-dione and from (40 × 10 −6 to 205 × 10 −6 ) mol·mol −1 for solid 3-(phenethylamino)-2-methylnaphthalene-1,4-dione. The experimental solubility was validated using three approaches, estimating the combined expanded uncertainty of measurement for each solubility data point, evaluating the thermodynamic consistency of the data utilizing a test based on the Gibbs–Duhem equation, and verifying the self-consistency by correlating the experimental solubility values with a semi-empirical model as a function of temperature, pressure and pure carbon dioxide density.

  14. Coprecipitation of {sup 14}C and Sr with carbonate precipitates: The importance of reaction kinetics and recrystallization pathways

    Energy Technology Data Exchange (ETDEWEB)

    Hodkin, David J. [School of Earth and Environment, University of Leeds, Leeds LS2 9JT (United Kingdom); Stewart, Douglas I. [School of Civil Engineering, University of Leeds (United Kingdom); Graham, James T. [National Nuclear Laboratory, Sellafield, Cumbria (United Kingdom); Burke, Ian T., E-mail: I.T.Burke@leeds.ac.uk [School of Earth and Environment, University of Leeds, Leeds LS2 9JT (United Kingdom)

    2016-08-15

    This study investigated the simultaneous removal of Sr{sup 2+} and {sup 14}CO{sub 3}{sup 2−} from pH > 12 Ca(OH){sub 2} solution by the precipitation of calcium carbonate. Initial Ca{sup 2+}:CO{sub 3}{sup 2−} ratios ranged from 10:1 to 10:100 (mM:mM). Maximum removal of {sup 14}C and Sr{sup 2+} both occurred in the system containing 10 mM Ca{sup 2+} and 1 mM CO{sub 3}{sup 2−} (99.7% and 98.6% removal respectively). A kinetic model is provided that describes {sup 14}C and Sr removal in terms of mineral dissolution and precipitation reactions. The removal of {sup 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 {sup 14}C back to solution. Sr{sup 2+} removal occurred as Ca{sup 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 {sup 90}Sr and {sup 14}C in radioactively contaminated waters (<$0.25 reagent cost per m{sup 3} treated). - Highlights: • 99.7% of {sup 14}C and 98.6% of Sr removed from aqueous solution by CaCO{sub 3} precipitation. • Remobilization of {sup 14}C observed during calcium carbonate recrystallization. • Sr displayed variable distribution coefficient (possibly affected by Ca:Sr ratio). • Reagent cost of $0.22/m{sup 3} of treated groundwater.

  15. 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)

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

    International Nuclear Information System (INIS)

    Prabakaran, K.; Fernandes, V.; McDonald, J.

    1996-01-01

    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

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

    International Nuclear Information System (INIS)

    Paula Eduardo, B. de; Cerri, C.C.

    1988-01-01

    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.) [pt

  18. Radiocarbon (14C) Constraints On The Fraction Of Refractory Dissolved Organic Carbon In Primary Marine Aerosol From The Northwest Atlantic

    Science.gov (United States)

    Beaupre, S. R.; Kieber, D. J.; Keene, W. C.; Long, M. S.; Frossard, A. A.; Kinsey, J. D.; Duplessis, P.; Chang, R.; Maben, J. R.; Lu, X.; Zhu, Y.; Bisgrove, J.

    2017-12-01

    Nearly all organic carbon in seawater is dissolved (DOC), with more than 95% considered refractory based on modeled average lifetimes ( 16,000 years) and characteristically old bulk radiocarbon (14C) ages (4000 - 6000 years) that exceed the timescales of overturning circulation. Although this refractory dissolved organic carbon (RDOC) is present throughout the oceans as a major reservoir of the global carbon cycle, its sources and sinks are poorly constrained. Recently, RDOC was proposed to be removed from the oceans through adsorption onto the surfaces of rising bubble plumes produced by breaking waves, ejection into the atmosphere via bubble bursting as a component of primary marine aerosol (PMA), and subsequent oxidation in the atmosphere. To test this mechanism, we used natural abundance 14C (5730 ± 40 yr half-life) to trace the fraction of RDOC in PMA produced in a high capacity generator at two biologically-productive and two oligotrophic hydrographic stations in the Northwest Atlantic Ocean during a research cruise aboard the R/V Endeavor (Sep - Oct 2016). The 14C signatures of PMA separately generated day and night from near-surface (5 m) and deep (2500 m) seawater were compared with corresponding 14C signatures in seawater of near-surface dissolved inorganic carbon (DIC, a proxy for recently produced organic matter), bulk deep DOC (a proxy for RDOC), and near-surface bulk DOC. Results constrain the selectivity of PMA formation from RDOC in natural mixtures of recently produced and refractory DOC. The implications of these results for PMA formation and RDOC biogeochemistry will be discussed.

  19. A survey of methods to immobilize tritium and carbon-14 arising from a nuclear fuel reprocessing plant

    International Nuclear Information System (INIS)

    Taylor, P.

    1991-02-01

    This report reviews the literature on methods to separate and immobilize tritium ( 3 H) and carbon-14 ( 14 C) released from U0 2 fuel in a nuclear fuel reprocessing plant. It was prepared as part of a broader review of fuel reprocessing waste management methods that might find future application in Canada. The calculated inventories of both 3 H and 14 C in used fuel are low; special measures to limit releases of these radionuclides from reprocessing plants are not currently in place, and may not be necessary in future. If required, however, several possible approaches to the concentration and immobilization of both radionuclides are available for development. Technology to control these radionuclides in reactor process streams is in general more highly developed than for reprocessing plant effluent, and some control methods may be adaptable to reprocessing applications

  20. Cambrian-lower Middle Ordovician passive carbonate margin, southern Appalachians: Chapter 14

    Science.gov (United States)

    Read, J. Fred; Repetski, John E.

    2012-01-01

    The southern Appalachian part of the Cambrian–Ordovician passive margin succession of the great American carbonate bank extends from the Lower Cambrian to the lower Middle Ordovician, is as much as 3.5 km (2.2 mi) thick, and has long-term subsidence rates exceeding 5 cm (2 in.)/k.y. Subsiding depocenters separated by arches controlled sediment thickness. The succession consists of five supersequences, each of which contains several third-order sequences, and numerous meter-scale parasequences. Siliciclastic-prone supersequence 1 (Lower Cambrian Chilhowee Group fluvial rift clastics grading up into shelf siliciclastics) underlies the passive margin carbonates. Supersequence 2 consists of the Lower Cambrian Shady Dolomite–Rome-Waynesboro Formations. This is a shallowing-upward ramp succession of thinly bedded to nodular lime mudstones up into carbonate mud-mound facies, overlain by lowstand quartzose carbonates, and then a rimmed shelf succession capped by highly cyclic regressive carbonates and red beds (Rome-Waynesboro Formations). Foreslope facies include megabreccias, grainstone, and thin-bedded carbonate turbidites and deep-water rhythmites. Supersequence 3 rests on a major unconformity and consists of a Middle Cambrian differentiated rimmed shelf carbonate with highly cyclic facies (Elbrook Formation) extending in from the rim and passing via an oolitic ramp into a large structurally controlled intrashelf basin (Conasauga Shale). Filling of the intrashelf basin caused widespread deposition of thin quartz sandstones at the base of supersequence 4, overlain by widespread cyclic carbonates (Upper Cambrian lower Knox Group Copper Ridge Dolomite in the south; Conococheague Formation in the north). Supersequence 5 (Lower Ordovician upper Knox in the south; Lower to Middle Ordovician Beekmantown Group in the north) has a basal quartz sandstone-prone unit, overlain by cyclic ramp carbonates, that grade downdip into thrombolite grainstone and then storm

  1. Carbon-14 activity of fallout in Araucaria angustifolia annual growth rings, from Arapoti, Parana State, Brazil

    International Nuclear Information System (INIS)

    Lisi, Claudio Sergio; Pessenda, Luiz Carlos Ruiz; Tomazello Filho, Mario

    2000-01-01

    During the period of nuclear tests between 1950 and 1960, an input of artificial 14 C (fallout effect) occurred in the natural reservoirs. 14 C determinations in the Northern Hemisphere showed values of Δ 14 C up to 960 in the year of 1964. To determine the fallout 14 C activity in Brazil, wood samples from Araucaria angustifolia (Bert.) O. Kuntze, Araucariaceae, were collected in Arapoti-PR (24 deg 11 S , 49 deg 58 O ). The annual tree rings were selected by dendrochronology. The cellulose was extracted and its 14 C activity determined by liquid scintillation method. The results showed a significant increase of the Δ 14 C up to 590 in 1965, about 60% higher than the natural activity, gradually decreasing after the end of nuclear tests. These results were correlated with those obtained in the Northen Hemisphere and will be used in the studies of CO 2 mechanisms distribuition to the atmosphere and other natural reservoirs. (author)

  2. Large-scale Patterns of 14C Age of Bulk Organic Carbon and Various Molecular Components in Grassland Soils

    Science.gov (United States)

    Jia, J.; Liu, Z.; Cao, Z.; Chen, L.; He, J. S.; Haghipour, N.; Wacker, L.; Eglinton, T. I.; Feng, X.

    2017-12-01

    Unraveling the fate of organic carbon (OC) in soils is essential to understanding the impact of global changes on the global carbon cycle. Previous studies have shown that while various soil OC components have different decomposability, chemically labile OC can have old 14C ages. However, few studies have compared the 14C age of various soil OC components on a large scale, which may provide important information on the link between the age or turnover of soil OC components to their sources, molecular structures as well as environmental variables. In this project, a suite of soil profiles were sampled along a large-scale transect of temperate and alpine grasslands across the Tibetan and Mongolian Plateaus in China with contrasting climatic, vegetation and soil properties. Bulk OC and source-specific compounds (including fatty acids (FAs), diacids (DAs) and lignin phenols) were radiocarbon-dated to investigate the age and turnover dynamics of different OC pools and the mechanisms controlling their stability. Our results show that lignin phenols displayed a large 14C variability. Short-chain (C16, 18) FAs sourced from vascular plants as well as microorganisms were younger than plant-derived long-chain FAs and DAs, indicating that short-chain FAs were easier to be decomposed or newly synthesized. In the temperate grasslands, long-chain DAs were younger than FAs, while the opposite trend was observed in the alpine grasslands. Preliminary correlation analysis suggests that the age of short-chain FAs were mainly influenced by clay contents and climate, while reactive minerals, clay or silt particles were important factors in the stabilization of long-chain FAs, DAs and lignin phenols. Overall, our study provided a unique 14 C dataset of soil OC components in grasslands, which will provide important constraints on soil carbon turnover in future investigations.

  3. Abiotic and bioaugmented granular activated carbon for the treatment of 1,4-dioxane-contaminated water.

    Science.gov (United States)

    Myers, Michelle A; Johnson, Nicholas W; Marin, Erick Zerecero; Pornwongthong, Peerapong; Liu, Yun; Gedalanga, Phillip B; Mahendra, Shaily

    2018-06-04

    1,4-Dioxane is a probable human carcinogen and an emerging contaminant that has been detected in surface water and groundwater resources. Many conventional water treatment technologies are not effective for the removal of 1,4-dioxane due to its high water solubility and chemical stability. Biological degradation is a potentially low-cost, energy-efficient approach to treat 1,4-dioxane-contaminated waters. Two bacterial strains, Pseudonocardia dioxanivorans CB1190 (CB1190) and Mycobacterium austroafricanum JOB5 (JOB5), have been previously demonstrated to break down 1,4-dioxane through metabolic and co-metabolic pathways, respectively. However, both CB1190 and JOB5 have been primarily studied in laboratory planktonic cultures, while most environmental microbes grow in biofilms on surfaces. Another treatment technology, adsorption, has not historically been considered an effective means of removing 1,4-dioxane due to the contaminant's low K oc and K ow values. We report that the granular activated carbon (GAC), Norit 1240, is an adsorbent with high affinity for 1,4-dioxane as well as physical dimensions conducive to attached bacterial growth. In abiotic batch reactor studies, 1,4-dioxane adsorption was reversible to a large extent. By bioaugmenting GAC with 1,4-dioxane-degrading microbes, the adsorption reversibility was minimized while achieving greater 1,4-dioxane removal when compared with abiotic GAC (95-98% reduction of initial 1,4-dioxane as compared to an 85-89% reduction of initial 1,4-dioxane, respectively). Bacterial attachment and viability was visualized using fluorescence microscopy and confirmed by amplification of taxonomic genes by quantitative polymerase chain reaction (qPCR) and an ATP assay. Filtered samples of industrial wastewater and contaminated groundwater were also tested in the bioaugmented GAC reactors. Both CB1190 and JOB5 demonstrated 1,4-dioxane removal greater than that of the abiotic adsorbent controls. This study suggests that

  4. Measured neutron carbon kerma factors from 14.1 MeV to 18 MeV

    International Nuclear Information System (INIS)

    Deluca, P.M.; Barschall, H.H.; McDonald, J.C.

    1985-01-01

    For A-150 tissue-equivalent plastic, the total neutron kerma is dominated by the hydrogen kerma. Tissue kerma is inferred with reasonable accuracy by normalization to the kerma factor ratio between tissue and A-150 plastic. Because of the close match in the hydrogen abundance in these materials, the principal uncertainty is due to the kerma factors of carbon and oxygen. We have measured carbon kerma factor values of 0.183+-0.015 10 -8 cGy cm 2 and 0.210+-0.016 10 -8 cGy cm 2 at 14.1-MeV and 15-MeV neutron energy, respectively. A preliminary value of 0.297+-0.03 10 -8 cGy cm 2 has been determined at 17.9 MeV. A recent microscopic cross section measurement of the (n,n'3α) reaction in carbon at 14.1-MeV energy gives a kerma factor of 0.184+-0.019 10 -8 cGy cm 2 in agreement with the present result

  5. Measured neutron carbon kerma factors from 14.1 MeV to 18 MeV

    International Nuclear Information System (INIS)

    Deluca, P.M. Jr.; Barschall, H.H.; Haight, R.C.; McDonald, J.C.

    1984-01-01

    For A-150 tissue-equivalent plastic, the total neutron kerma is dominated by the hydrogen kerma. Tissue kerma is inferred with reasonable accuracy by normalization to the kerma factor ratio between tissue and A-150 plastic. Because of the close match in the hydrogen abundance in these materials, the principal uncertainty is due to the kerma factors of carbon and oxygen. We have measured carbon kerma factor values of 0.183 +- 0.015 10 -8 cGy cm 2 and 0.210 +- 0.16 10 -8 cGy cm 2 at 14.1-MeV and 15-MeV neutron energy, respectively. A preliminary value of 0.297 +- 0.03 10 -8 cGy cm 2 has been determined at 17.9 MeV. A recent microscopic cross section measurement of the (n,n'3α) reaction in carbon at 14.1-MeV energy gives a kerma factor of 0.184 +- 0.019 10 8 cGy cm 2 in agreement with the present result. 9 refs., 4 figs., 2 tabs

  6. Reproducibility of measurement of the environmental carbon-14 samples prepared by the gel suspension method

    International Nuclear Information System (INIS)

    Ohura, Hirotaka; Wakabayashi, Genichiro; Nakamura, Kouji; Okai, Tomio; Matoba, Masaru; Kakiuchi, Hideki; Momoshima, Noriyuki; Kawamura, Hidehisa.

    1997-01-01

    Simple liquid scintillation counting technique for the assay of 14 C in the environment was developed. This technique was done by using gel suspension method, in which sample preparation is very simple and requires no special equipments. The reproducibility of this technique was considered and it was shown that the gel suspension method had enough reproducibility to monitor the environmental 14 C. (author)

  7. Relationship between carbon-14 concentrations in tree-ring cellulose and atmospheric CO2

    International Nuclear Information System (INIS)

    Yamada, Yoshimune; Yasuike, Kaeko; Komura, Kazuhisa

    2008-01-01

    Concentrations of organically-bound 14 C in the tree-ring cellulose of a Japanese Cedar (Cryptomeria japonica) grown in a rural region of Kanazawa, Ishikawa prefecture, Japan (36.5degN, 136.7degE), were measured for the ring-years from 1989 to 1998 to study relationship between 14 C concentrations in tree-ring cellulose and atmospheric CO 2 in a narrow region. An interesting result in comparing our data of tree-ring cellulose with those of atmospheric CO 2 is that the 14 C concentration in tree-ring cellulose was close to the corresponding average from mid-June to early September of 14 C concentrations in atmospheric CO 2 . Furthermore, the 14 C concentrations in tree-ring cellulose were found to be merely influenced by the drastic decrease of 14 C concentrations in atmospheric CO 2 in winter, which might be caused by air pollution from the Asian continent and additional local fossil fuel contribution. These results suggest that the 14 C concentration in tree-ring cellulose for a given growing year reflects the 14 C concentrations of atmospheric CO 2 during the warm summer months. (author)

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

    International Nuclear Information System (INIS)

    Classic, K.L.; Schwenk, W.F.; Haymond, M.W.

    1986-01-01

    In vivo estimates of protein metabolism in many are often made by oral or intravenous administration of leucine or its ∼-ketoacid, ∼-ketoisocaproate, labeled with 14 C or 3 H. Previous estimates of radiation dose from such tracers have been based on the measurement of 14 CO 2 in breath. Using measurements of the decay of 3 H or 14 C 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- 14 C]KIC (or [1- 14 C]leucine) and 0.11 mrad/ + Ci for ]4,5- 3 H]leucine (or [ 3 H]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

  9. Spatial analysis of Carbon-14 dynamics in a wetland ecosystem (Duke Swamp, Chalk River Laboratories, Canada)

    International Nuclear Information System (INIS)

    Yankovich, T.L.; King-Sharp, K.J.; Carr, J.; Robertson, E.; Killey, R.W.D.; Beresford, N.A.; Wood, M.D.

    2014-01-01

    A detailed survey was conducted to quantify the spatial distribution of 14 C in Sphagnum moss and underlying soil collected in Duke Swamp. This wetland environment receives 14 C via groundwater pathways from a historic radioactive Waste Management Area (WMA) on Atomic Energy Canada Limited (AECL)'s Chalk River Laboratories (CRL) site. Trends in 14 C specific activities were evaluated with distance from the sampling location with the maximum 14 C specific activity (DSS-35), which was situated adjacent to the WMA and close to an area of groundwater discharge. Based on a spatial evaluation of the data, an east-to-west 14 C gradient was found, due to the influence of the WMA on 14 C specific activities in the swamp. In addition, it was possible to identify two groups of sites, each showing significant exponential declines with distance from the groundwater source area. One of the groups showed relatively more elevated 14 C specific activities at a given distance from source, likely due to their proximity to the WMA, the location of the sub-surface plume originating from the WMA, the presence of marsh and swamp habitat types, which facilitated 14 C transport to the atmosphere, and possibly, 14 C air dispersion patterns along the eastern edge of the swamp. The other group, which had lower 14 C specific activities at a given distance from the groundwater source area, included locations that were more distant from the WMA and the sub-surface plume, and contained fen habitat, which is known to act as barrier to groundwater flow. The findings suggest that proximity to source, groundwater flow patterns and habitat physical characteristics can play an important role in the dynamics of 14 C being carried by discharging groundwater into terrestrial and wetland environments. - Highlights: • Groundwater represents an important source of volatile radionuclides to wetlands. • Habitat type influenced 14 C transport from sub-surface to surface environments. • C-14 specific

  10. Temperature dependence of desoxyribosylation of pyrimidine derivatives labelled with carbon-14 and tritium

    International Nuclear Information System (INIS)

    Pritasil, L.; Filip, J.

    1977-01-01

    The effect of the temperature and concentration of the enzyme preparation from Escherichia coli B on the reaction of pyrimidine bases with 2-desoxy-α-D-riboso-l-phosphate or α-D-riboso-l-phosphate was studied. It was found that at +2 deg C and low enzyme concentration higher yields of nucleosides are obtained than at the commonly used temperature of 37 deg C. The reaction time, however, must be protracted. The prepared [2- 14 C] uridine, 2'-deoxy[2- 14 C] uridine and [2- 14 C] thymidine had a high specific activity and radiochemical purity

  11. Acylation of lithiated trimethylsilyl malonates and esters applied to the synthesis of molecules of biological interest, labelled with carbon 14

    International Nuclear Information System (INIS)

    Gorichon, Liliane

    1978-01-01

    This research thesis first reports an attempt to generalise the method of acylation of lithiated trimethylsilyl (TMS) malonates by introduction of new organic functions into the radical. This leads to the synthesis of some alkaloids such as nicotine and contine. The author also shows that fat acids can be labelled with carbon 14 in any position of the carbon chain. Thus, acylation of these malonates have been performed by using different acid chlorides. Then, the author reports attempts to simplify this method by using α-lithiated trimethylsilyl esters instead of malonates. He reports attempts of acylation of TMS isobutyrate, TMS proprionate and TMS acetate, by using different radioactive acid chlorides (benzoyl chloride, nicotinoyl chloride, lauryl chloride, and oleyl chloride). The author finally shows that both methods are equivalent by synthesising muscalure from TMS butylmalonate as well as from TMS hexanoate

  12. Quantification of Helicobacter pylori infection in gastritis and ulcer disease using a simple and rapid carbon-14-urea breath test

    International Nuclear Information System (INIS)

    Debongnie, J.C.; Pauwels, S.; Raat, A.; de Meeus, Y.; Haot, J.; Mainguet, P.

    1991-01-01

    Gastric urease was studied isotopically in 230 patients with biopsy-proven normal mucosa or chronic gastritis, including 59 patients with ulcer disease. Carbon-14-urea was given in 25 ml of water without substrate carrier or nutrient-dense meal, and breath samples were collected over a 60-min period. The amount of 14CO2 excreted at 10 min was independent of the rate of gastric emptying and was not quantitatively influenced by the buccal urease activity. The 10-min 14CO2 values discriminated well between Helicobacter pylori positive and negative patients (94% sensitivity, 89% specificity) and correlated with the number of organisms assessed by histology. The test was a good predictor of chronic gastritis (95% sensitivity and 96% specificity), and a quantitative relationship was observed between 14CO2 values and the severity and activity of the gastritis. In H. pylori positive patients, breath 14CO2 was found to be similar in patients with and without ulcer disease, suggesting that the number of bacteria is not a determining factor for the onset of ulceration

  13. Quantification of Helicobacter pylori infection in gastritis and ulcer disease using a simple and rapid carbon-14-urea breath test

    Energy Technology Data Exchange (ETDEWEB)

    Debongnie, J.C.; Pauwels, S.; Raat, A.; de Meeus, Y.; Haot, J.; Mainguet, P. (Department of Nuclear Medicine, University of Louvain Medical School, Brussels (Belgium))

    1991-06-01

    Gastric urease was studied isotopically in 230 patients with biopsy-proven normal mucosa or chronic gastritis, including 59 patients with ulcer disease. Carbon-14-urea was given in 25 ml of water without substrate carrier or nutrient-dense meal, and breath samples were collected over a 60-min period. The amount of 14CO2 excreted at 10 min was independent of the rate of gastric emptying and was not quantitatively influenced by the buccal urease activity. The 10-min 14CO2 values discriminated well between Helicobacter pylori positive and negative patients (94% sensitivity, 89% specificity) and correlated with the number of organisms assessed by histology. The test was a good predictor of chronic gastritis (95% sensitivity and 96% specificity), and a quantitative relationship was observed between 14CO2 values and the severity and activity of the gastritis. In H. pylori positive patients, breath 14CO2 was found to be similar in patients with and without ulcer disease, suggesting that the number of bacteria is not a determining factor for the onset of ulceration.

  14. Isolation of carbon 14 labelled amino acids by biosynthesis in maize plants (zea mais L.)

    International Nuclear Information System (INIS)

    Carreras, N.; Mazon, M.P.

    1983-01-01

    A method of obtaining 14 C labelled amino acids by biosynthesis in maize plants which had assimilated 14 CO 2 , has been assayed. The plants were labelled for 60 minutes with 14 CO 2 produced from Ba 14 CO 3 (specific activity of 148 KBq/μmol). An extract of the soluble compounds was obtained with 80% ethanol and the amino acids were separated from the rest of the soluble compounds by ion exchange chromatography on column of Dowex 50-X8 resin. Finally, seventeen amino acids were isolated and identified from the purified extract. The acid amino acids were separated in anionic column (Dowex 1-X8) and the neutral and basic amino acids in cationic columns (Dowex 50-X4). (author)

  15. 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)

  16. Carbon 14, carbon 13 and oxygen 18 in carbonate sediments from lake Titicaca. Preliminary estimates of sedimentation rate and paleoclimatological attempt

    International Nuclear Information System (INIS)

    Fontes, J.-C.; Boulange, Bruno; Rodrigo, L.-A.

    1981-01-01

    Stable isotope and radiocarbon measurements in carbonates from Titicaca lake indicate equilibrium with lake water and atmospheric CO 2 . Average sedimentation rate is close to 0,5 mm.yr -1 for the last millenium which was marked by large fluctuations of the hydrologic balance and lake level [fr

  17. Carbon 14, carbon 13 and oxygen 18 in carbonate sediments from Lake Titicaca. Preliminary estimates of sedimentation rate and paleoclimatological attempt

    Energy Technology Data Exchange (ETDEWEB)

    Fontes, J.C. (Paris-11 Univ., 91 - Orsay (France)); Boulange, B. (Orstom, 75 - Paris (France)); Rodrigo, L.A. (Universidad Mayor de San Andres, La Paz (Bolivia). Lab. de Fisica Cosmica de Chacaltaya)

    1981-07-06

    Stable isotope and radiocarbon measurements in carbonates from Lake Titicaca indicate equilibrium with lake water and atmospheric CO/sub 2/. Average sedimentation rate is close to 0,5 mm.yr/sup -1/ for the last millenium which was marked by large fluctuations of the hydrologic balance and lake level.

  18. Synthesis of methyl ((chloro-2 ethyl)-3 nitroso-3 Ureido)-3 Didesoxy-2,3. alpha. -D-Arabino-hexopyrannoside labelled with carbon-14 or carbon-13 (CY 233 - SR 90008). Synthese du methyl ((chloro-2 ethyl)-3 nitroso-3 Ureido)-3 Didesoxy-2,3. alpha. -D-Arabino-hexopyrannoside marque au carbone-14 ou carbone-13 (CY 233 - SR 90008)

    Energy Technology Data Exchange (ETDEWEB)

    Sion, R.; Schumer, A.; Durme, E. van (Sanofi Recherche, Brussels (Belgium)); Gouyette, A. (Centre de Lutte Contre le Cancer Gustave-Roussy, 94 - Villejuif (France)); Geslin, M.; Fournier, J.P.; Roger, P. (Sanofi Recherche, Montrouge (France). Inst. Choay); Berger, Y. (Sanofi Recherche, Montpellier (France))

    1990-06-01

    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 {sup 14}C on (a) the carbonyl group of the urea in four stages starting with {sup 14}COCl{sub 2}, (b) the second carbon of the chloroethyl group in four stages starting with ({sup 14}C) ethanolamine, and (c) on the methyl group on the anomeric centre of the carbohydrate in three stages starting with {sup 14}CH{sub 3}OH. The final position was also labelled with {sup 13}C starting with {sup 13}CH{sub 3}OH. These differently labelled compounds are suitable for mechanistic studies of antitumour activity. (author).

  19. Metabolism of tritium- and carbon-14-labeled tiamulin in dogs, rats, and pigs.

    Science.gov (United States)

    Dreyfuss, J; Singhvi, S M; Shaw, J M; Egli, P; Ross, J J; Czok, R; Nefzger-Biessels, M; Battig, F; Schuster, I; Schmook, F

    1979-05-01

    The metabolism of tiamulin hydrogen fumarate, labeled with 3H, 14C, or both, was studied in dogs, rats, and weanling pigs. After a dose of radiolabeled tiamulin, all three species excreted more radioactivity in feces (via bile) than in urine. Dogs absorbed 86% of a single oral dose of tiamulin-3H, and the disposition of the compound was similar after a single or multiple dosage regimen. The ratio of antimicrobial activity to total radioactivity in dog plasma was only about 0.25, and was still less in dog urine. After dosing with tiamulin-14C, rats and pigs excreted at least 1% of the dose as 14CO2 in expired air. In dual-labeled studies, pigs excreted less total 14C than 3H and had greater residues of 14C than 3H in edible tissues, blood, and plasma. After the administration of tiamulin-14C to pigs, radioactivity was incorporated into liver glycogen, indicating metabolic cleavage of the side chain of tiamulin. Tiamulin-3H is the isotopically-labeled compound of choice for studying metabolism and tissue residues in animals.

  20. 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

    ' and 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...... with 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 seeds, whereas...

  1. Effect of altered intraraceme competition on carbon-14-labeled assimilate and abscisic acid in soybean

    International Nuclear Information System (INIS)

    Spollen, W.G.; Wiebold, W.J.; Glenn, S.

    1986-01-01

    Abscission probability varies among floral positions within soybean [Glycine max (L.) Merr.] racemes. Field grown soybean plants were used to determine the distribution of translocated 14 C-labeled photosynthate and abscisic acid (ABA) among reproductive structures differing for abscission probability. The effect of proximal pods on the translocation of 14 C-labeled photosynthate to and ABA concentration in distal pods (floral positions 3 and above) was also evaluated. Treatments consisted of removing or not removing the two proximal pods (floral positions 1 and 2) from the major racemes at nodes 8 and 10 in 1982 and 8, 10, and 12 in 1983. Six days after treatment in 1982 and 12 days after treatment in 1983. 14 C-translocation from the leaf at the node of interest was determined after exposure to 14 CO 2 . On the same day, distal pods were collected for determination of ABA by gas chromatography. For untreated plants, proximal and distal pods accounted for 50 and 7% of the translocated 14 C, respectively. Proximal pod removal had no effect on 14 C retained by the source leaf (72%) or the concentration of ABA in seeds. Concentration of ABA in pod wall of distal pods was increased by proximal pod removal in only one instance. Amount of 14 C translocated to distal pods and distal pod specific activity were not altered by proximal pod removal in 1982 but were increased in 1983. The different treatment effect between years may indicate that distal pods undergo a period of adjustment after proximal pod removal. An understanding of processes that occur during the adjustment period may be necessary before the mechanism of soybean reproductive abscission is known

  2. The long-term trend of carbon-14 level in Japan

    International Nuclear Information System (INIS)

    Yoshikazu Inoue; Tetsuo Iwakura

    1993-01-01

    The long-term trend of the specific activity of 14 C in terms of dpm/gC from 1942 to 1991 in the natural environment in Japan was obtained as baseline data by analyzing plant components so as to evaluate the collective effective dose. It was deduced that the specific activity of 14 C in plants reflected well that of atmospheric 14 CO 2 . Uniform distribution of the specific activity in plant among species as well as the production places was confirmed. The Suess effect was observed clearly for a period of 10 years from the late 1960's. The 14 C level was at about 13.7 dpm/gC due to cosmic ray production in 1940's, and reached a peak of about 24.5 dpm/gC in 1963 due to nuclear weapons testing and decreased to 15.6 dpm/gC in 1991. Fermented alcohol proved to be a convenient indicator for measuring the annual mean specific activity of 14 C in the atmosphere. (3 figs.)

  3. 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.)

  4. Carbon-14-labeled 2,3,7,8- and 1,2,7,8-tetrachlorodibenzofuran

    International Nuclear Information System (INIS)

    Gray, A.P.; McClellan, W.J.; Dipinto, V.M.

    1981-01-01

    Both 2,3,7,8- and 1,2,7,8- tetrachlorodibenzofuran -U 14 C, specific activity 57 mCi/mmol, have been obtained in low yield but at > 98% purity via Pschorr cyclization of o-phenoxyaniline -U 14 C, chlorination of the resultant dibenzofuran and separation of the tetrachloro isomers by hplc. The lower yields obtained in the Pschorr cyclization of 'hot' o-phenoxyaniline in comparison with the 'cold' material are postulated to result from enhanced homolytic relative to heterolytic cleavage of the 'hot' diazonium ion leading to a 'hot' free radical which polymerizes. The completely anomalous results observed in the attempted palladium acetate-mediated cyclization of diphenyl ether- U 14 C are likewise interpreted in terms of the intervention of a 'hot' free radical. (author)

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

    International Nuclear Information System (INIS)

    Uschkoreit, J.

    1979-01-01

    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) [de

  6. Gas-phase noncovalent functionalization of carbon nanotubes with a Ni(II) tetraaza[14]annulene complex

    Science.gov (United States)

    Basiuk, Vladimir A.; Henao-Holguín, Laura Verónica; Álvarez-Zauco, Edgar; Bassiouk, María; Basiuk, Elena V.

    2013-04-01

    The noncovalent functionalization of carbon nanotubes (CNTs) with aromatic polyazamacrocyclic compounds, based on π-π-interactions, keeps the intrinsic electronic structure of CNTs totally intact and allows for combining unique properties of the two interacting components. In addition to porphyrins and phthalocyanines, there are other, simpler compounds exhibiting similar properties, potentially useful for photovoltaic, catalytic and electrochemical applications: for example, tetraaza[14]annulenes. Many of them are highly thermally stable, which makes it possible to employ physical vapor deposition for the preparation of macrocycle-nanotube hybrids. One of such compounds is Ni(II) complex of 5,7,12,14-tetramethyldibenzo-1,4,8,11-tetraazacyclotetradeca-3,5,7,10,12,14-hexaene (also called Ni(II)-tetramethyldibenzotetraaza[14]annulene, or NiTMTAA for simplicity). In the present work, we attempted the noncovalent functionalization of both single-walled and multi-walled CNTs with NiTMTAA in the gas phase at two selected temperatures of 220 and 270 °C, which does not require the use of organic solvents and therefore can be considered as ecologically friendly. The nanohybrids obtained were characterized by means of scanning and transmission electron microscopy, energy dispersive X-ray, Fourier-transform infrared and Raman spectroscopy, as well as thermogravimetric analysis. An additional insight into the structure of adsorption complexes of NiTMTAA on CNTs was provided from density functional theory and molecular mechanics calculations.

  7. Gas-phase noncovalent functionalization of carbon nanotubes with a Ni(II) tetraaza[14]annulene complex

    Energy Technology Data Exchange (ETDEWEB)

    Basiuk, Vladimir A., E-mail: basiuk@nucleares.unam.mx [Instituto de Ciencias Nucleares, Universidad Nacional Autónoma de México, Circuito Exterior, Ciudad Universitaria, 04510, México D.F. (Mexico); Henao-Holguín, Laura Verónica [Instituto de Ciencias Nucleares, Universidad Nacional Autónoma de México, Circuito Exterior, Ciudad Universitaria, 04510, México D.F. (Mexico); Álvarez-Zauco, Edgar [Facultad de Ciencias, Universidad Nacional Autónoma de México, Circuito Exterior C.U., 04510, México D.F. (Mexico); Bassiouk, María [Instituto de Ciencias Nucleares, Universidad Nacional Autónoma de México, Circuito Exterior, Ciudad Universitaria, 04510, México D.F. (Mexico); Basiuk, Elena V. [Centro de Ciencias Aplicadas y Desarrollo Tecnológico, Universidad Nacional Autónoma de México, Circuito Exterior, Ciudad Universitaria, 04510, México D.F. (Mexico)

    2013-04-01

    The noncovalent functionalization of carbon nanotubes (CNTs) with aromatic polyazamacrocyclic compounds, based on π–π-interactions, keeps the intrinsic electronic structure of CNTs totally intact and allows for combining unique properties of the two interacting components. In addition to porphyrins and phthalocyanines, there are other, simpler compounds exhibiting similar properties, potentially useful for photovoltaic, catalytic and electrochemical applications: for example, tetraaza[14]annulenes. Many of them are highly thermally stable, which makes it possible to employ physical vapor deposition for the preparation of macrocycle–nanotube hybrids. One of such compounds is Ni(II) complex of 5,7,12,14-tetramethyldibenzo-1,4,8,11-tetraazacyclotetradeca-3,5,7,10,12, 14-hexaene (also called Ni(II)-tetramethyldibenzotetraaza[14]annulene, or NiTMTAA for simplicity). In the present work, we attempted the noncovalent functionalization of both single-walled and multi-walled CNTs with NiTMTAA in the gas phase at two selected temperatures of 220 and 270 °C, which does not require the use of organic solvents and therefore can be considered as ecologically friendly. The nanohybrids obtained were characterized by means of scanning and transmission electron microscopy, energy dispersive X-ray, Fourier-transform infrared and Raman spectroscopy, as well as thermogravimetric analysis. An additional insight into the structure of adsorption complexes of NiTMTAA on CNTs was provided from density functional theory and molecular mechanics calculations.

  8. Gas-phase noncovalent functionalization of carbon nanotubes with a Ni(II) tetraaza[14]annulene complex

    International Nuclear Information System (INIS)

    Basiuk, Vladimir A.; Henao-Holguín, Laura Verónica; Álvarez-Zauco, Edgar; Bassiouk, María; Basiuk, Elena V.

    2013-01-01

    The noncovalent functionalization of carbon nanotubes (CNTs) with aromatic polyazamacrocyclic compounds, based on π–π-interactions, keeps the intrinsic electronic structure of CNTs totally intact and allows for combining unique properties of the two interacting components. In addition to porphyrins and phthalocyanines, there are other, simpler compounds exhibiting similar properties, potentially useful for photovoltaic, catalytic and electrochemical applications: for example, tetraaza[14]annulenes. Many of them are highly thermally stable, which makes it possible to employ physical vapor deposition for the preparation of macrocycle–nanotube hybrids. One of such compounds is Ni(II) complex of 5,7,12,14-tetramethyldibenzo-1,4,8,11-tetraazacyclotetradeca-3,5,7,10,12, 14-hexaene (also called Ni(II)-tetramethyldibenzotetraaza[14]annulene, or NiTMTAA for simplicity). In the present work, we attempted the noncovalent functionalization of both single-walled and multi-walled CNTs with NiTMTAA in the gas phase at two selected temperatures of 220 and 270 °C, which does not require the use of organic solvents and therefore can be considered as ecologically friendly. The nanohybrids obtained were characterized by means of scanning and transmission electron microscopy, energy dispersive X-ray, Fourier-transform infrared and Raman spectroscopy, as well as thermogravimetric analysis. An additional insight into the structure of adsorption complexes of NiTMTAA on CNTs was provided from density functional theory and molecular mechanics calculations.

  9. The preparation of nucleotides uniformly labelled with carbon-14 by biosinthetic methods. Isolation of adenilic, uridilic, cytidilic and guanlic acids, from the alkaline hydrolisate of escherichia coli RNA

    International Nuclear Information System (INIS)

    Garcia Pineda, D.; Pacheco Lopez, J.

    1978-01-01

    A method is described for the preparation and analysis of adenilic, uridilic, cytidylic and guanilic acids, labelled with carbon 14. Escherichia coli cells have been labelled by growing them in media containing glucose-carbon 14 as their only source of carbon. RNA is isolated from the cells, and after hydrolisis of the molecule the resulting nucleotides are separated by gel filtration and exchange chromatography. Chemical and radiochemical purity of the isolated nucleotides is determined and also its specific radioactivity. The distribution of radioactivity incorporated in the cell among different groups of molecular species is analyse. (author)

  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.

    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)

    Lawrie, K.W.M.; Novelli, C.E.A.; Saunders, David

    1995-01-01

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

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

    Energy Technology Data Exchange (ETDEWEB)

    Lawrie, K.W.M.; Novelli, C.E.A.; Saunders, David [SmithKline Beecham Pharmaceuticals Research and Development, Harlow (United Kingdom). Synthetic Isotope Chemistry Dept.; Coates, W.J. [SmithKline Beecham Pharmaceuticals Research and Development, Welwyn (United Kingdom)

    1995-09-01

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

  13. Simple analytical technique for liquid scintillation counting of environmental carbon-14 using gel suspension method

    International Nuclear Information System (INIS)

    Okai, Tomio; Wakabayashi, Genichiro; Nagao, Kenjiro; Matoba, Masaru; Ohura, Hirotaka; Momoshima, Noriyuki; Kawamura, Hidehisa

    2000-01-01

    A simple analytical technique for liquid scintillation counting of environmental 14 C was developed. Commercially available gelling agent, N-lauroyl-L -glutamic -α,γ-dibutylamide, was used for the gel-formation of the samples (gel suspension method) and for the subsequent liquid scintillation counting of 14 C in the form of CaCO 3 . Our procedure for sample preparation is much simpler than that of the conventional methods and requires no special equipment. Self absorption, stability and reproducibility of gel suspension samples were investigated in order to evaluate the characteristics of the gel suspension method for 14 C activity measurement. The self absorption factor is about 70% and slightly decrease as CaCO 3 weight increase. This is considered to be mainly due to the absorption of β-rays and scintillation light by the CaCO 3 sample itself. No change of the counting rate for the gel suspension sample was observed for more than 2 years after the sample preparation. Four samples were used for checking the reproducibility of the sample preparation method. The same values were obtained for the counting rate of 24 C activity within the counting error. No change of the counting rate was observed for the 're-gelated' sample. These results show that the gel suspension method is appropriate for the 14 C activity measurement by the liquid scintillation counting method and useful for a long-term preservation of the sample for repeated measurement. The above analytical technique was applied to actual environmental samples in Fukuoka prefecture, Japan. Results obtained were comparable with those by other researchers and appear to be reasonable. Therefore, the newly developed technique is useful for the routine monitoring of environmental 14 C. (author)

  14. Effects of entrainment through Oconee Nuclear Station on carbon-14 assimilation rates of phytoplankton

    International Nuclear Information System (INIS)

    Kreh, T.V.; Derwort, J.E.

    1976-01-01

    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

  15. 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

  16. 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, Bernhard; Braakhekke, M.C.|info:eu-repo/dai/nl/343063689; Guggenberger, Georg; Schrumpf, Marion; Reichstein, Markus

    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

  17. Sources of Respired Carbon in a Northern Minnesota Ombrotrophic Spruce Bog: Preliminary 14C Results from the SPRUCE Site.

    Science.gov (United States)

    Guilderson, T. P.; McNicol, G.; Machin, A.; Hanson, P. J.; McFarlane, K. J.; Osuna, J. L.; Pett-Ridge, J.; Singleton, M. J.

    2014-12-01

    A significant uncertainty in future land-surface carbon budgets is the response of wetlands to climate change. A corollary and related question is the future net climate (radiative) forcing impact from wetlands. Active wetlands emit both CO2 and CH4 to the atmosphere. CH4 is, over a few decades, a much more potent greenhouse gas than CO2. CO2 has a longer atmospheric lifetime and a longer 'tail' to its radiative influence. Whether wetlands are a net source or sink of atmospheric carbon under future climate change will depend on ecosystem response to rising temperatures and elevated CO2. The largest uncertainty in future wetland C-budgets, and their climate forcing is the stability of the large below-ground carbon stocks, often in the form of peat, and the partitioning of CO2 and CH4 released via ecosystem respiration. In advance of a long-term experimental warming and elevated CO2 manipulation at the DOE Spruce and Peatland Responses Under Climatic and Environmental Change (SPRUCE) site in the Marcell Experimental Forest, we have characterized the source of respired carbon used for both the production of CO2 and CH4. Samples were collected in early June, late July, and will be collected in early September from three large (~1.1 m2, ~0.5m3) chambers from the control plot, and two of the experimental plots selected for heating (+9°C, +4.5°C). Early June fluxes from the three chambers were ~5500 mgC-m-2-d-1 and ~16 mgC-m-2-d-1 for CO2 and CH4 respectively. Radiocarbon analysis of CO2 and CH4 indicate that the source for the respired carbon is for the most part recent, with most 14C values between 30 and 40‰ - i.e., carbon that was photosynthetically fixed in the last few years. In concert with rising air and ground temperatures fluxes in late July increased to ~6500 mgC-m-2-d-1 and ~86 mgC-m-2-d-1. Although deep-heating was initiated in mid to late June we hypothesize that the July respiration signal is dominated by the regular seasonal cycle of natural warming

  18. Background carbon-14 levels in UK foodstuffs, 1981-1995, based upon a 1992 survey

    International Nuclear Information System (INIS)

    Otlet, R.L.; Walker, A.J.; Fulker, M.J.; Collins, C.

    1997-01-01

    Knowledge of the current 'natural' background level is important to 14 C-related studies, especially dose assessments in the vicinity of and distant from nuclear establishments since its value must be subtracted from measured levels to determine local enhancement. Although measurements have been made world-wide to monitor the decline of the background level, from its peak in the early 1960s to the present, there exists a paucity of precise data for UK natural materials. Accordingly this study was carried out to establish an average figure for the 'natural' 14 C level in foodstuffs in 1992 from a survey of materials collected from a wide range of sites over England and Wales, using this single year value, to infill missing years prior to 1992 and to extrapolate from some years afterwards. Results are presented from the survey, and for the derived extrapolation with comparison made with measurements from other laboratories. (Author)

  19. Carbon-14 methylation of the 2-methylbutyryl side chain of mevinolin and its analogs

    International Nuclear Information System (INIS)

    Prakash, S.R.; Ellsworth, R.L.

    1988-01-01

    A one step procedure for the preparation of three labeled mevinolin analogs possessing the 2,2-dimethylbutyryloxy side chain is described. Three lactones were converted into potassium salts of their corresponding di or trihydroxy carboxylic acids from which anionic ester enolates were generated and alkylated with [ 14 ]methyl iodide. Workup and purification by reverse phase HPLC provided the three radiochemically pure mevinolin analogs. The labeled lactones were converted into ammonium salts of their corresponding di or trihydroxy acids. (author)

  20. A Chlorine-36 and Carbon-14 Study of the Role of Chlorine in the Forest Ecosystem

    Czech Academy of Sciences Publication Activity Database

    Matucha, Miroslav; Gryndler, Milan; Forczek, Sándor; Schröder, P.; Bastviken, D.; Rohlenová, Jana; Uhlířová, H.; Fuksová, Květoslava

    2007-01-01

    Roč. 50, č. 1 (2007), s. 1-3 ISSN 0362-4803 R&D Projects: GA ČR GA522/02/0874; GA ČR GA526/05/0636 Institutional research plan: CEZ:AV0Z50380511 Keywords : [14C]-synthesis * labeled compounds * tetrahydrocyclopenta[b]indol-3-yl acetic acid Subject RIV: EF - Botanics Impact factor: 1.142, year: 2007

  1. Differential cross sections for carbon neutron elastic and inelastic scattering from 8.0 to 14.5 MeV

    Energy Technology Data Exchange (ETDEWEB)

    Haouat, G.; Lachkar, J.; Patin, Y.; Sigaud, J.; Cocu, F.

    1975-06-01

    Differential elastic and inelastic cross sections for fast neutrons scattered by carbon have been measured between 8.0 and 14.5 MeV. No experimental results on {sup 12}C seem to have been reported, at this time, between 9 and 14 MeV. A complete and consistent set of data on carbon, including total, elastic and inelastic, (n,α) and (n,n'3α) cross sections, is now available for energies below 14.5MeV.

  2. Development of Carbon-14 Waste Destruction and Recovery System Using AC Plasma Torch Technology Final Report CRADA No. TC02108.0

    Energy Technology Data Exchange (ETDEWEB)

    Althouse, P. [Lawrence Livermore National Lab. (LLNL), Livermore, CA (United States); McKannay, R. H. [Lawrence Livermore National Lab. (LLNL), Livermore, CA (United States)

    2017-08-15

    This was a collaborative effort between Lawrence Livermore National Security, LLC as manager and operator of Lawrence Livermore National Laboratory (LLNL) and ISOFLEX USA (ISOFLEX), to 1) develop and test a prototype waste destruction system ("System") using AC plasma torch technology to break down and drastically reduce the volume of Carbon-14 (C-14) contaminated medical laboratory wastes while satisfying all environmental regulations, and 2) develop and demonstrate methods for recovering 99%+ of the carbon including the C-14 allowing for possible re-use as a tagging and labeling tool in the biomedical industry.

  3. Carbon-14 urea breath test for the diagnosis of Campylobacter pylori associated gastritis

    International Nuclear Information System (INIS)

    Marshall, B.J.; Surveyor, I.

    1988-01-01

    Urease in the human gastric mucosa is a marker for infection with Campylobacter pylori (CP), an organism suspected of causing chronic gastritis and peptic ulceration. To detect gastric urease, we examined 32 patients who were being evaluated for possible peptic ulcer disease. Fasting patients were given 10 microCi (370 kBq) of 14 C-labeled urea. Breath samples were collected in hyamine at intervals between 1 and 30 min. The amount of 14 C collected at these times was expressed as: body weight X (% of administered dose of 14 C in sample)/(mmol of CO 2 collected). The presence of C. pylori colonization was also determined by examination of multiple endoscopic gastric biopsy specimens. On average, patients who were proven to have C. pylori infection exhaled 20 times more labeled CO 2 than patients who were not infected. The difference between infected patients and C. pylori negative control patients was highly significant at all time points between 2 and 30 min after ingestion of the radionuclide (p less than 0.0001). The noninvasive urea breath is less expensive than endoscopic biopsy of the stomach and more accurate than serology as a means of detecting Campylobacter pylori infection. Because the test detects actual viable CP organisms, it can be used to confirm eradication of the bacterium after antibacterial therapy

  4. 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.

    2015-01-01

    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 cm3 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

  5. 14C dating of freshwater carbonate sediments with special reference to calcareous tufas and laminated lake sediments

    International Nuclear Information System (INIS)

    Pazdur, M.F.

    1992-09-01

    The sequence of laminated sediment of the lake Gosciaz, Poland, covers more than 13,000 years and is actually the longest sequence known so far. Besides of reconstructing past environmental changes, this sequence offers an excellent possibility for studying natural C-14 variations and calibrating the C-14 time scale in a range beyond 6,000 years B.P. The floating varve chronology based on previously taken sediment cores which cover a period of 9,682 years, has been improved by this study. Relative water level changes of the lake during the past 11,500 years have been reconstructed by means of C-14 and C-13 measurements carried out on carbonate fractions of the lake sediments. Periodical variations in the width of annual layers were found. The periods identified are 11 years and 22 years (solar cycle), 35 years (Bruckner cycle), and 200 years. The ratio of summer layer width and the total width of the annual layer shows secular changes which correlate with paleotemperature records. The duration of the Younger Dryas period was determined by combining the floating varve chronology with isotope and pollen analyses of the sediment material. A value of 1,500 years was found. The study also included radiocarbon dating of calcareous tufa taken from different study areas. 26 refs, 26 figs, 6 tabs

  6. Carbon-14 immobilization via the Ba(OH)28H2O process

    International Nuclear Information System (INIS)

    Haag, G.L.; Nehls, J.W. Jr.; Young, G.C.

    1982-01-01

    The airborne release of 14 C from various nuclear facilities has been identified as a potential biohazard due to the long half-life of 14 C (5730 yrs) and the ease in which it may be assimilated into the biosphere. At Oak Ridge National Laboratory, technology is under development, as part of the Airborne Waste Management Program, for the removal and immobilization of this radionuclide. Prior studies have indicated that the 14 C will likely exist in the oxidized form as CO 2 and will contribute slightly to the bulk CO 2 concentration of the gas stream, which is airlike in nature (approx. 330 ppMv CO 2 ). The technology under development utilizes the CO 2 - Ba(OH) 2 8H 2 O gas-solid reaction with the mode of gas-solid contacting being a fixed bed. The product, BaCO 3 , possessing excellent thermal and chemical stability, prerequisites for the long-term disposal of nuclear wastes. For optimal process operation, studies have indicated that an operating window of adequate size does exist. When operating within the window, high CO 2 removal efficiency (effluent concentrations 99%), and an acceptable pressure drop across the bed (3 kPa/m at 13 cm/s superficial velocity) are possible. This paper will address three areas of experimental investigation. These areas are (1) micro-scale studies on 150-mg samples to provide information concerning surface properties, kinetics, and equilibrium vapor pressures, (2) macro-scale studies on large fixed beds (4.2 kg reactant) to determine the effects of humidity, temperature, and gas flow-rate upon bed pressure drop and CO 2 breakthrough, and (3) the design, construction, and initial operation of a pilot unit capable of continuously processing a 34 m 3 /h (20 ft 3 /min) air-based gas stream

  7. Age determination of ground-waters by means of carbon 14

    International Nuclear Information System (INIS)

    Eichinger, L.

    1982-02-01

    At present the age determination of ground-waters aged between 1,500 and approximately 40,000 years is only possible by measuring their 14 C 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 13 C, D, 18 O, 3 H, 85 Kr and the 39 Ar contents, about the ph value, temperature and the principal ions. (DG) [de

  8. Selected radionuclides. Tritium, carbon-14, krypton-85, strontium-90, iodine, caesium 137, radon, plutonium

    International Nuclear Information System (INIS)

    1983-01-01

    The release of radioactive materials to the environment potentially exposes populations to ionizing radiation and increases the risk of incurring deleterious health effects. The associations of released amounts to effects establish the health criteria for radionuclides. This report provides background information in establishing such health criteria for 14 C, 85 Kr, 90 Sr, 137 Cs, Radon, Plutonium, Iodine and Tritium, including environmental behaviour, sources, transport to man and dosimetry. A brief summary of the general aspects of radiation effects and of radiation protection considerations is presented

  9. Automatic counting and recording unit used for dating by the carbon 14 method; Ensemble de comptage et d'impression automatique utilise pour la datation par la methode du carbone 14

    Energy Technology Data Exchange (ETDEWEB)

    Albertinoli, P; Galliot, J; Thommeret, J [Commissariat a l' Energie Atomique, Saclay (France). Centre d' Etudes Nucleaires. Centre Scientifique de Monaco, Monte Carlo

    1969-07-01

    A description is given of the unit used by the 'Centre Scientifique de Monaco' for low-level beta counting and fitted for radioactive dating by the Carbon 14 method. Built entirely by the laboratory in 1964, on the basis of electronic techniques then recent, it has worked without failure since that time. The proportional counter, its high-voltage negative supply, and the counting chains with visual and printing records are detailed by means of 38 figures which reproduce the counter and the electronic circuits. These are contained in two standard 5 U.I structures. The low-voltage power supply of the whole unit is carried out by plus 12 volts and minus 12 volts storage batteries, buffered on a charger connected on the 110 V alternative line. The proportional counter described is filled with CO{sub 2} under one atmosphere pressure and permits the dating of carbonaceous samples with a maximum of 30.000 + 1.000 years (background 3.96 c.p.m. ) within a moderate time (72 hours). (authors) [French] L'ensemble de comptage pour radioactivite beta a bas niveau, destine a la datation par la methode du carbone 14, utilise au Centre Scientifique de Monaco, est decrit. Entierement construit au laboratoire en 1964, sur la base de techniques electroniques alors recentes, il fonctionne depuis cette date sans defaillance. Le compteur proportionnel, son alimentation haute tension negative et les chaines de comptage transistorisees a affichage et impression sont detailles par 38 schemas reproduisant le compteur et les divers circuits electroniques. Ceux-ci sont contenus dans deux chassis standard 5 UI. L'alimentation basse tension de l'ensemble est obtenue par batteries plus 12 et moins 12 volts montees en tampon sur chargeur alimente par le reseau. Le compteur proportionnel decrit, rempli de CO2 sous une atmosphere, permet de dater les echantillons carbones avec un maximum de 30.000 + 1.000 ans (bruit de fond: 3,96 c.p.m. ) en un temps raisonnable (72 heures). (auteur)

  10. Accidental Carbon Monoxide Poisonings in Adana, Turkey: A 14-year Study

    Directory of Open Access Journals (Sweden)

    Murat Darçın

    2017-03-01

    Full Text Available Aim: Carbon monoxide (CO is often referred to as the “silent killer” because its victims cannot see it, smell it or taste it. CO is responsible for a large percentage of the accidental poisonings and deaths reported throughout the world. CO poisoning therefore is considered a serious global health threat. The aim of the present study was to describe the cases of CO poisoning in a rural areas of Adana, Turkey between 2002 and 2015 based on data collected from incident reports. Methods: The cases of accidental CO poisoning were statistically analyzed. During that period, 74 incidents occurred and 154 people were poisoned by accidental CO poisoning. Results: The results of this analysis indicate that men and adults aged ≥65 years were more likely to die from CO poisoning than others. The number of CO poisoning cases was highest during the heating season. The majority (72% of poisoning resulting in hospitalization with a life-threatening condition or death occurred within the home. Conclusion: CO poisoning is a serious danger. People must be informed about this hazard. By educating risk groups about the dangers of CO poisoning, it is possible to save many lives as well as reduce the health risks.

  11. Influence of a carbamate pesticide on growth, respiration (/sup 14/C)-carbon metabolism and symbiosis of a Rhizobium sp

    Energy Technology Data Exchange (ETDEWEB)

    Sekar, T; Balasubramanian, A [Tamil Nadu Agricultural Univ., Coimbatore (India)

    1979-04-01

    Addition of aldicarb (2 methyl-2(methyl thio) propionaldehyde-O-methyl carbamoyl oxime) in the growth medium enhanced the growth of Rhizobium sp. (cowpea group) at 2ppm level while an inhibition was observed at the normal (5 ppm) and higher (10 ppm) concentrations. Respiration of the cells was also inhibited by 5 and 10 ppm levels of the chemical eventhough a stimulation was observed at 2 ppm (lower) concentration. The insecticide, when incorporated at 5 and 10 ppm levels in the medium increased the /sup 14/C-glucose incorporation and considerably altered the assimilation of the radioactive carbon in different fractions of rhizobium cells. Soil application of this insecticide (Temik 10 G) reduced the number of nodules formed and the total nitrogen content in cowpea plants inoculated with the Rhizobium sp. but enhanced the dry matter production of cowpea plants.

  12. Investigation on the distribution of tritium and carbon-14 in the amino acids of labelled green algae (Scenedesmus Quadricauda ssp.)

    International Nuclear Information System (INIS)

    Nuernberger, E.; Clausen, E.; Kistner, G.

    1982-01-01

    Green algae (Scenedesmus quadricauda ssp. subspicatus), labelled twice tritium and carbon-14, showed an incorporation of nuclides into the cell mass of 0.02% and 95%, respectively. The distribution of radioactivity in the individual amino acids was examined in a protein fraction with special emphasis on the essential amino acids in view of their following incorporation into the next link of the aquatic food chain (Daphnia). The highest values were found in glutamine and asparagine acids as well as in the essential amino acids leucine and arginine, which are amino acids with a relatively high amount of non exchangeable H-positions per molecule and, therefore, a relatively high and stable labelling. (author)

  13. Utilization of [1-14C]carbon of glycine of high glycine diet fed young and old rats

    International Nuclear Information System (INIS)

    Petzke, K.J.; Albrecht, V.; Medovar, B.Ya.; Pisarczuk, K.L.; Grigorov, Yu.G.

    1987-01-01

    The incorporation of radioactivity from [1- 14 C]glycine was studied in various organ (serum, liver, muscle) fractions (acid soluble, proteins, lipids, liver glycogen) and carbon dioxide in rats fed with isonitrogenous isocaloric purfied diets. The diets contained 30% casein (control), gelatin (exchange of half of the 30% casein) or glycine (corresponding level of glycine in relation to the gelatin diet). The incorporation of radioactivity into proteins was reduced by feeding high glycine diets in young (20-weeks-old) and old (18-month-old) rats in relation to the control diet. The modifications of the results for old animals may be partially explained on the base of a reduced protein turnover rate and adaptation to a high gelatin (glycine) diet. (author)

  14. Incorporation of 14C glucose into glycogen and glucose-6-phosphate dehydrogenase activity in rat brain following carbon monoxide intoxication

    International Nuclear Information System (INIS)

    Sikorska, M.; Gorzkowski, B.; Szumanska, G.; Smialek, M.

    1975-01-01

    Incorporation of 14 C glucose into glycogen and glucose-6-phosphate dehydrogenase activity in rat brain following carbon monoxide intoxication was studied. In brains of rats tested on the 20, 30 and 60th minute of exposure to CO and immediately after removal from the chamber the enzyme activity showed no essential deviation from the control level. In the group of rats tested 1 hour after taking them out from the chamber increase of the enzyme activity was noticed, amounting to about 33% of the control value. The brains tested 24 hours after exposure showed the largest increase of the enzyme activity by about 94%. In the next time periods, 48 and 72 hours after intoxication, the enzyme activity was decreasing. The glycogen content in brains of control animals increased 3 hours after CO intoxication by about 69%. The increase of glycogen synthesis was expressed by increase of the total radioactivity, which amounted to 160% of the control value. (Z.M.)

  15. The rates of carbon cycling in several soils from AMS14C measurements of fractionated soil organic matter

    International Nuclear Information System (INIS)

    Trumbore, S.E.; Bonani, G.; Wolfli, W.

    1990-01-01

    14 C mean residence times (MRT) of fractionated organic matter are reported for three pre-bomb soil profiles. Comparisons of organic matter extracted with acid and base showed that the longest MRTs were associated with the non-acid-hydrolysable fraction. The MRT of organic matter in a soil layer represents a combination of the rates of several processes, including decay to CO 2 and transport out of the layer. In some instances (notably in the A horizon of the Podzol soil studied in this paper), the MRT is dominated by the rate of transport, rather than the rate of decay. Thus it is important to use the distribution and balance of carbon in the soil profile to assess the meaning of the MRT with respect to influencing atmospheric CO 2

  16. Interactions between 59Fe(14C)EDTA and soils containing calcium carbonate

    International Nuclear Information System (INIS)

    Hargitai-Toth, A.; Konya, J.

    1991-01-01

    Interaction between FeEDTA and calcareous soils was followed over a period of four weeks using a radiotracer technique, and a kinetic evaluation of the results was performed. 59 Fe served to determine the quantity of iron, 14 C to assay for EDTA and 45 Ca to measure calcium. During the experiment, i.e. within four weeks in case of the chernozem soil 61% and in case of the clayey meadow soil 51% of the iron chelate disappeared from the solution. The loss in soluble iron was partly due to a rapid sorption process of about an hour and partly due to the slow decomposition of FeEDTA to Fe(OH) 3 . The two processes could be separated using the Christiansen equation. (author) 9 refs.; 1 figs.; 2 tabs

  17. Extraction of carbon 14-labeled compounds from plant tissue during processing for electron microscopy

    International Nuclear Information System (INIS)

    Coetzee, J.; van der Merwe, C.F.

    1989-01-01

    Loss of 14 C-labeled compounds from bean leaf tissue was monitored during all the stages of routine specimen preparation. No significant differences in extraction were associated with the use of acetone, ethanol, or dioxane as dehydration fluids. Fixation at low temperature increased the loss of label. Prolonged fixation in glutaraldehyde increased the loss, but fixation in osmium solutions for periods as long as 4 hr had no influence on extraction. Buffer rinses and dehydration fluids caused appreciable amounts of label to be extracted. The use of propylene oxide as transition fluid resulted in low extraction. Some embedding media caused the loss of small amounts of labeled compounds, but one of the media tested (LR-white) extracted significant amounts of label

  18. Carbon-14 immobilization via the Ba(OH)2.8H2O process

    International Nuclear Information System (INIS)

    Haag, G.L.; Nehls, J.W. Jr.; Young, G.C.

    1983-03-01

    The airborne release of 4 C from varous nuclear facilities has been identified as a potential biohazard due to the long half-life of 14 C (5730 y) and the ease with which it may be assimilated into the biosphere. At ORNL, technology has been developed for the removal and immobilization of this radionuclide. Prior studies have indicated that 14 C will likely exist in the oxidized form as CO 2 and will contribute slightly to the bulk CO 2 concentration of the gas stream, which is airlike in nature (approx. 330 ppmv CO 2 ). The technology that has been developed utilizes the CO 2 -Ba(OH) 2 .8H 2 O gas-solid reaction with the mode of gas-solid contacting being a fixed bed. The product, BaCO 3 , possesses excellent thermal and chemical stability, prerequisites for the long-term disposal of nuclear wastes. For optimal process operation, studies have indicated that an operating window of adequate size does exist. When operating within the window, high CO 2 removal efficiency (effluent concentrations 99%), and an acceptable pressure drop across the bed (3 kPa/m at a superficial velocity of 13 cm/s) are possible. This paper addresses three areas of experimental investigation: (1) microscale studies on 150-mg samples to provide information concerning surface properties, kinetics, and equilibrium vapor pressures; (2) macroscale studies on large fixed beds (4.2 kg of reactant) to determine the effects of humidity, temperature, and gas flow rate upon bed pressure drop and CO 2 breakthrough; and (3) design, construction, and initial operation of a pilot unit capable of continuously processing a 34-m 3 /h (20-ft 3 /min) air-based gas stream

  19. 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.

  20. Preliminary study of lead isotopes in the carbonate-silica veins of Trench 14, Yucca Mountain, Nevada

    International Nuclear Information System (INIS)

    Zartman, R.E.; Kwak, L.M.

    1993-01-01

    The sub-vertical carbonate-silica veins filling the Bow Ridge Fault, where exposed in Trench 14 on the east side of Yucca Mountain, carry a lead isotopic signature that can be explained in terms of local sources. Two isotopically distinguishable--silicate and carbonate--fractions of lead are recognized within the vein system as well as in overlying surficial calcrete deposits. The acid-insoluble silicate fraction is contributed largely from the decomposing Miocene volcanic tuff, which forms the wall rock of the fault zone and is a ubiquitous component of the overlying soil. Lead contained in the silicate fraction approaches in isotopic composition that of the Miocene volcanic rocks of Yucca Mountain, but diverges from it in some samples by being more enriched in uranogenic isotopes. The carbonate fraction of lead in both vein and calcrete samples resides dominantly in the HCl- and CH 3 COOH-soluble calcite. HCl evidently also attacks and removes lead from silicate phases, but the milder CH 3 COOH dissolution procedure oftentimes identifies a significantly more radiogenic lead in the calcite. Wind-blown particulate matter brought to the area from Paleozoic and Late Proterozoic limestones in surrounding mountains may be the ultimate source of the calcite. Isotopically more uniform samples suggest that locally the basaltic ash and other volcanic rock have contributed most of the lead to both fractions of the vein system. An important finding of this study is that the data does not require the more exotic mechanisms or origins that have been proposed for the veins. Instead, the remarkably similar lead isotopic properties of the veins to those of the soil calcretes support their interpretation as a surficial, pedogenic phenomenon

  1. Synthesis of organic substances labelled with {sup 14}C and {sup 35}S; Syntheses de molecules organiques marquees par le carbone-14 et le soufre-35

    Energy Technology Data Exchange (ETDEWEB)

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

    1958-07-01

    After a brief history of the development of the Section des Molecules marquees of the Frenchmic Energy Commission, the author gives an outline of the synthesis of the following labelled compounds: benzene {sup 14}C-6; phenyl-p-fluorophenyl, thienyl-2 {beta} alanines {beta} {sup 14}C; noradrenaline {beta} {sup 14}C (arterenol {beta} {sup 14}C), dotriacontane {sup 14}C-16-17, aminoethane sulfinic acid (hypotaurine {sup 35}S). (author)Fren. [French] Apres un bref historique du developpement de la Section des Molecules marquees du Commissariat a l'Energie Atomique fran is, l'auteur donne un resume des syntheses des composes marques suivants: benzene {sup 14}C-6; phenyl-p-fluorophenyl, thienyl-2 {beta} alamines {beta} {sup 14}C; noradrenaline {beta} {sup 14}C (arterenol {beta} {sup 14}C), dotriacontane {sup 14}C-16-17, acide aminoethane sulfinique (hypotaurine {sup 35}S). (auteur)

  2. 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.

  3. The synthesis of the insecticides Aldrin and Dieldrin labelled with carbon-14 at high specific activity; Synthese des insecticides aldrine et dieldrine marques au carbone-14 de haute activite specifique; Sintez insektitsidnogo aldrina i dildrina, mechennykh uglerodom-14 pri vysokoj udel'noj aktivnosti; Sintesis de los insecticidas aldrin y dieldrin de elevada actividad especifica marcados con carbono-14

    Energy Technology Data Exchange (ETDEWEB)

    Thomas, Daniel J; Kilner, A Edward [Radiochemical Centre, UKAEA, Amersham, Bucks (United Kingdom)

    1962-03-15

    Aldrin is the trade name given by Shell Chemicals to 1, 2, 3, 4, 10, 10-hexachloro-1, 4, 4a, 5, 8, 8a-hexahydro-exo-1, 4-endo-5, 8-dimethanonapthalene. Acetylene-1, 2-C{sup 14} is converted successively to tetrachloroethane and trichloroethylene, and this is condensed with carbon tetrachloride by the Prins reaction in the presence of aluminium chloride to octachlorocyclopentene. Dechlorination gives hexachlorocyclopentadiene which undergoes a Diels-Alder addition to bicyclo(2, 2, 1) hepta-2,5-diene to give aldrin-C{sup 14} in 12% yield from barium carbonate. Oxidation of Aldrin gives the 6,7 epoxide, Dieldrin, in 87% yield. The paper includes an account of the separation of octachlorocyclopentene from the crude product of the Prins reaction by gas-liquid chromatography and of the separation of Aldrin and Dieldrin on a small preparative scale by reversed-phase paper chromatography. (author) [French] Aldrine est la denomination commerciale par laquelle la Shell Chemicals designe l'hexachloro-1, 2, 3, 4, 10, 10-hexahydro-1, 4, 4a, 5, 8, 8a-exo-endo-1,4- dimethano-5, 8-naphtalene. L'acetylene-1,2-C{sup 14} est successivement transforme en terachloroethane et en trichloroethylene, lequel se condense avec le tetrachlorure de carbone, par la reaction de Prins, en presence de chlorure d'aluminium, pour donner de l'octachlorocyclopentene. La dechloruration fournit de l'hexachlorocyclopentadiene, lequel, par une synthese de Diels-Alder, se transforme en bicyclohepta(2, 2, 1)-diene-2, 5 pour donner de l'aldrine-C{sup 14}, avec un rendement de 12% par rapport au carbonate de baryum. L'oxydation de l'aldrine donne l'epoxyde-6 7-(dieldrine), avec un rendement de 87%. Les auteurs decrivent, en outre, la separation de l'octachlorocyclopentene par chromatographie gaz-liquide, a partir du produit brut de la reaction de Prins, ainsi que la separation de l'aldrine et de la dieldrine, en petite quantite, par chromatographie sur papier a phase renversee. (author) [Spanish] Aldrin es el

  4. The triply-ionized carbon forest from eBOSS: cosmological correlations with quasars in SDSS-IV DR14

    Science.gov (United States)

    Blomqvist, Michael; Pieri, Matthew M.; du Mas des Bourboux, Hélion; Busca, Nicolás G.; Slosar, Anže; Bautista, Julian E.; Brinkmann, Jonathan; Brownstein, Joel R.; Dawson, Kyle; de Sainte Agathe, Victoria; Guy, Julien; Percival, Will J.; Pérez-Ràfols, Ignasi; Rich, James; Schneider, Donald P.

    2018-05-01

    We present measurements of the cross-correlation of the triply-ionized carbon (CIV) forest with quasars using Sloan Digital Sky Survey Data Release 14. The study exploits a large sample of new quasars from the first two years of observations by the Extended Baryon Oscillation Spectroscopic Survey (eBOSS). The CIV forest is a weaker tracer of large-scale structure than the Lyα forest, but benefits from being accessible at redshifts zfit to the quasar-CIV cross-correlations for the CIV forest and the SiIV forest, the CIV redshift-space distortion parameter is βCIV=0.27 ‑0.14 ‑0.26 +0.16 +0.34 and its combination with the CIV linear transmission bias parameter is bCIV(1+βCIV)=‑0.0183 ‑0.0014 ‑0.0029 +0.0013 +0.0025 (1σ and 2σ statistical errors) at the mean redshift z=2.00. Splitting the sample at z=2.2 to constrain the bias evolution with redshift yields the power-law exponent γ=0.60±0.63, indicating a significantly weaker redshift-evolution than for the Lyα forest linear transmission bias. Additionally, we demonstrate that CIV absorption has the potential to be used as a probe of baryon acoustic oscillations (BAO). While the current data set is insufficient for a detection of the BAO peak feature, the final quasar samples for redshifts 1.4

  5. Micro-syntheses for the use of carbon 13 or carbon 14. Micro-preparations of methyl alcohol, methyl iodide, and sodium acetate labeled in the methyl group; Microsyntheses pour l'emploi de carbone 13 ou de carbone 14. Micropreparations d'alcool methylique, d'iodure de methyle et d'acetate de sodium marque sur le groupement methyle

    Energy Technology Data Exchange (ETDEWEB)

    Baret, C; Pichat, L

    1951-11-01

    Apparatus and technique are described in detail for (1) reduction of CO{sub 2} to CH{sub 3}OH with LiAlH{sub 4}, (2) conversion of the methanol to CH{sub 3}I by HI, (3) formation of the Mg Grignard reagent, and (4) addition of inactive CO{sub 2} to form CH{sub 3}COOH. All these operations have been carried out on 0.005 moles. Methyl-labeled Na acetate has been prepared in 67% yield based on the Ba{sup 14}CO{sub 3} used as starting material. (author) [French] Description detaillee d'une technique deja connue pour la reduction du gaz carbonique en alcool methylique par LiAlH{sub 4}. Conversion du methanol en iodure de methyle. Ce dernier transforme en reactif de Grigard, et carbonate, fournit de l'acide acetique. Toutes ces operations on ete effectuees sur 5 x 10{sup -3} moles. La methode a ete appliquee a la synthese d'acetate de sodium marque par le groupement methyle par {sup 14}C avec un rendement global de 67% base sur le carbonate de baryum radioactif mis en oeuvre. (auteurs)

  6. 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)

    Sion, R.; Schumer, A.; Durme, E. van; Gouyette, A.; Geslin, M.; Fournier, J.P.; Roger, P.

    1990-01-01

    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 14 C on a) the carbonyl group of the urea in four stages starting with 14 COCl 2 , b) the second carbon of the chloroethyl group in four stages starting with [ 14 C] ethanolamine, and c) on the methyl group on the anomeric centre of the carbohydrate in three stages starting with 14 CH 3 OH. The final position was also labelled with 13 C starting with 13 CH 3 OH. These differently labelled compounds are suitable for mechanistic studies of antitumour activity. (author)

  7. Estimation of radiation dosage and transmutation effect of 14C involved in measuring rate of albumin synthesis with 14C-carbonate

    International Nuclear Information System (INIS)

    Yap, A.H.; Hafkenscheid, J.C.M.; Goossens, C.M.I.C.; Buys, W.C.A.M.; Binkhorst, R.A.; Van Tongeren, J.H.M.

    1975-01-01

    For direct measurement of the rate of albumin synthesis, Na 2 14 CO 3 was used intravenously. The assessment of the radiation hazard involved in the study was based on the knowledge of the minimum dose of Na 2 14 CO 3 necessary for a sufficient incorporation of 14 C in the guanidine-C of arginine in albumin to obtain measurable radioactivity. By measurement of expired 14 CO 2 and excreted 14 C-urea in the urine during a 5-hr period following intravenous administration of Na 2 14 CO 3 in five subjects, some quantitative data on 14 C retention and radiation dosage were obtained. In comparison with animal studies, the rate of expiration of 14 CO 2 in man is slower. About 50 percent of the total radioactivity injected was lost through the respiratory route in the first hour. The total amount of expired 14 C during the 5 hr of investigation was about 75 percent of the injected dose for the five subjects. The amount of 14 C excreted as urinary 14 C-urea during the 5 hr of investigation is very small in comparison with the expired 14 C; it was only about 0.5 percent of the dose injected. The total absorbed radiation dose after complete elimination of 14 C from the body was calculated with various assumptions. The extra risk of genetic damage due to disintegration of retained 14 C in comparison with that of natural 14 C in the body during 30 living years is about 50 percent. (U.S.)

  8. Calculation of carbon-14, chlorine-37, and deuterium kinetic isotope effects in the solvolysis of tert-butyl chloride

    International Nuclear Information System (INIS)

    Burton, G.W.; Sims, L.B.; Wilson, J.C.; Fry, A.

    1977-01-01

    In the solvolysis of tert-butyl chloride, satisfactory α-carbon-14, β-deuterium, and chlorine kinetic isotope effects (KIE) may be calculated for a productlike transition state characterized by bond orders n/sub C Cl/ = 0.2, n/sub C C/ = 1.18, and n/sub C H/ = 0.94, employing a diagonal valence force field, provided that allowance is made for hydrogen-bonded solvation of the developing chloride ion with n/sub Cl H/ approx. 0.05 (approx. 7 kcal/mole hydrogen bonds). The effect of the three solvating molecules appears to be to increase the ''effective'' mass of the incipient chloride ion and to decrease the loss of zero-point energy in going to the transition state. Reaction coordinates more complicated than a simple heterolysis of the carbon-chlorine bond appear to be unnecessary and there is no advantage in employing force fields more complex than a simple valence force field containing only diagonal elements for both the reactant and the transition state model. The structural and bonding features of the proposed transition state are in accord with earlier more qualitative conclusions concerning the polar nature and productlike character of the transition state, and provide a reasonable explanation of the kinetic and equilibrium isotope effects (EIE) for the reaction. An alternative transition state model involving weak solvent nucleophilic assistance provides reasonable calculated values for the KIE, but the EIE strongly suggest the importance of solvation of the leaving group which, together with the hyperconjugation of the β hydrogens, provides a preferred explanation of the tert-butyl solvolysis results

  9. 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)

    Vende, L.

    2012-01-01

    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 ( 14 CO 2 , HT...) or in solution ( 14 CO 3 2- , 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)

  10. Ventilation of the deep Greenland and Norwegian seas: evidence from krypton-85, tritium, carbon-14 and argon-39

    International Nuclear Information System (INIS)

    Smethie, W.M. Jr.; Ostlund, H.G.; Loosli, H.H.

    1986-01-01

    On leg 5 of the TTO expedition, the distributions of 85 Kr, tritium, 14 C, 39 Ar, 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 85 Kr, tritium, 14 C and 39 Ar 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)

  11. Apportioning bacterial carbon source utilization in soil using 14 C isotope analysis of FISH-targeted bacterial populations sorted by fluorescence activated cell sorting (FACS): 14 C-FISH-FACS.

    Science.gov (United States)

    Gougoulias, Christos; Meade, Andrew; Shaw, Liz J

    2018-02-19

    An unresolved need in microbial ecology is methodology to enable quantitative analysis of in situ microbial substrate carbon use at the population level. Here, we evaluated if a novel combination of radiocarbon-labelled substrate tracing, fluorescence in situ hybridisation (FISH) and fluorescence-activated cell sorting (FACS) to sort the FISH-targeted population for quantification of incorporated radioactivity ( 14 C-FISH-FACS) can address this need. Our test scenario used FISH probe PSE1284 targeting Pseudomonas spp. (and some Burkholderia spp.) and salicylic acid added to rhizosphere soil. We examined salicylic acid- 14 C fate (mineralized, cell-incorporated, extractable and non-extractable) and mass balance (0-24 h) and show that the PSE1284 population captured ∼ 50% of the Nycodenz extracted biomass 14 C. Analysis of the taxonomic distribution of the salicylic acid biodegradation trait suggested that PSE1284 population success was not due to conservation of this trait but due to competitiveness for the added carbon. Adding 50KBq of 14 C sample -1 enabled detection of 14 C in the sorted population at ∼ 60-600 times background; a sensitivity which demonstrates potential extension to analysis of rarer/less active populations. Given its sensitivity and compatibility with obtaining a C mass balance, 14 C-FISH-FACS allows quantitative dissection of C flow within the microbial biomass that has hitherto not been achieved. © 2018 Society for Applied Microbiology and John Wiley & Sons Ltd.

  12. Preparation of a lipopolysaccharide from ''Escherichia coli 0111a, 0111b, K58: H21'' bacterial wall, labeled with carbon-14

    International Nuclear Information System (INIS)

    Garcia Pineda, D.; Solano, M.A.

    1980-01-01

    A brief description is made of the morphological and chemical structure of lipopolysaccharides, as well as its occurence in nature and its mechanisms of action. It is emphasized the usefulness of the labelled lipopolysaccharide for actual biochemical and biomedical research. The method for the labelling, isolation and purification of carbon-14 lipopolysaccharide is described. (auth.)

  13. Radioactive carbon-14 dating of ground waters in IPEN for evaluation of water resources in Rio Grande do Norte and Parana basin

    International Nuclear Information System (INIS)

    Chandra, U.; Pereira, M.C.

    1986-01-01

    14 C dating of deep ground waters from Potiguar basin and Parana basin was carried out to identify zones of recharge. In all 28 samples, five from Potiguar basin and 23 from Parana basin were analyzed for 14 C. The methods of sample collection and analysis are described. The analysis consists of transforming carbon of the sample to benzene, by synthesis process involving four steps i.e. production of carbon dioxide, production of lithium carbide, hydrolysis to acetylene and catalytic polymerization to bezene. The specific activity of the synthertized benzene is measured by liquid scintillation counting. The corrections for initial 14 C content have been made by using the model of Vogel. (Author) [pt

  14. 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

  15. 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)

    Sandberg, Johannes

    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

  16. J-type Carbon Stars: A Dominant Source of {sup 14}N-rich Presolar SiC Grains of Type AB

    Energy Technology Data Exchange (ETDEWEB)

    Liu, Nan; Nittler, Larry R.; Alexander, Conel M. O’D.; Wang, Jianhua [Department of Terrestrial Magnetism, Carnegie Institution for Science, Washington, DC 20015 (United States); Stephan, Thomas; Boehnke, Patrick; Davis, Andrew M.; Trappitsch, Reto; Pellin, Michael J., E-mail: nliu@carnegiescience.edu [Department of the Geophysical Sciences, The University of Chicago, Chicago, IL 60637 (United States)

    2017-07-20

    We report Mo isotopic data of 27 new presolar SiC grains, including 12 {sup 14}N-rich AB ({sup 14}N/{sup 15}N > 440, AB2) and 15 mainstream (MS) grains, and their correlated Sr and Ba isotope ratios when available. Direct comparison of the data for the MS grains, which came from low-mass asymptotic giant branch (AGB) stars with large s -process isotope enhancements, with the AB2 grain data demonstrates that AB2 grains show near-solar isotopic compositions and lack s -process enhancements. The near-normal Sr, Mo, and Ba isotopic compositions of AB2 grains clearly exclude born-again AGB stars, where the intermediate neutron-capture process ( i -process) takes place, as their stellar source. On the other hand, low-mass CO novae and early R- and J-type carbon stars show {sup 13}C and {sup 14}N excesses but no s -process enhancements and are thus potential stellar sources of AB2 grains. Because both early R-type carbon stars and CO novae are rare objects, the abundant J-type carbon stars (10%–15% of all carbon stars) are thus likely to be a dominant source of AB2 grains.

  17. J-type Carbon Stars: A Dominant Source of 14 N-rich Presolar SiC Grains of Type AB

    Energy Technology Data Exchange (ETDEWEB)

    Liu, Nan; Stephan, Thomas; Boehnke, Patrick; Nittler, Larry R.; Alexander, Conel M. O’D.; Wang, Jianhua; Davis, Andrew M.; Trappitsch, Reto; Pellin, Michael J.

    2017-07-20

    We report Mo isotopic data of 27 new presolar SiC grains, including 12 N-14-rich AB (N-14/N-15 > 440, AB2) and 15 mainstream (MS) grains, and their correlated Sr and Ba isotope ratios when available. Direct comparison of the data for the MS grains, which came from low-mass asymptotic giant branch (AGB) stars with large s-process isotope enhancements, with the AB2 grain data demonstrates that AB2 grains show near-solar isotopic compositions and lack s-process enhancements. The near-normal Sr, Mo, and Ba isotopic compositions of AB2 grains clearly exclude born-again AGB stars, where the intermediate neutron-capture process (i-process) takes place, as their stellar source. On the other hand, low-mass CO novae and early R-and J-type carbon stars show C-13 and N-14 excesses but no s-process enhancements and are thus potential stellar sources of AB2 grains. Because both early R-type carbon stars and CO novae are rare objects, the abundant J-type carbon stars (10%-15% of all carbon stars) are thus likely to be a dominant source of AB2 grains.

  18. Helium-4 characteristics of groundwaters from Central Australia: Comparative chronology with chlorine-36 and carbon-14 dating techniques

    Science.gov (United States)

    Kulongoski, Justin T.; Hilton, David R.; Cresswell, Richard G.; Hostetler, Stephen; Jacobson, Gerry

    2008-01-01

    SummaryHelium isotope and concentration characteristics were determined for a suite of groundwater samples from the Amadeus Basin in Central Australia. Two study areas include a wellfield south of Alice Springs, and the Dune Plains and Mututjulu aquifers near Uluru. Measurements of 36Cl/Cl and 14C on the same sample suite enable us to assess the relative applicability of the three groundwater chronometers over a range of anticipated groundwater residence times (ages), and to investigate possible causes of discordant 'ages' derived from the different groundwater dating techniques. Results from the analyses of 39 groundwater samples reveal helium-4 ( 4He) concentrations that range from 0.80 to 98.8 (×10 -7 cm 3 STP g -1 H 2O) in the Alice Springs samples, and from 0.47 to 65.6 (×10 -7 cm 3 STP g -1 H 2O) in the Uluru samples. 4He concentrations yield uncorrected groundwater residence times (i.e. time since recharge) of between modern to >2500 ka (near Alice Springs) and modern to 1600 ka (near Uluru) assuming an effective porosity of 20%, and uranium and thorium contents of 1.7 and 6.1 ppm, respectively. 36Cl/Cl ratios on the same samples range from 93 to 158 (×10 -15) (near Alice Springs) and from 80 to 335 (×10 -15) (near Uluru) representing groundwater residence times near Alice Springs from modern to >200 ka, and from modern to >300 ka near Uluru. Percent modern carbon (pmc) on the same samples ranged from 64.9 to 12.5 pmc near Alice Springs, and from 93.5 to 30 ka. For the Amadeus Basin groundwater samples, the 4He method (uncorrected) over-estimates groundwater residence time compared to 36Cl and 14C techniques. This implies the presence of an extraneous He component or basal flux of He ( J0). To reconcile groundwater 4He and 14C residence times, it is necessary to adopt J0 values between 0 and 30 (×10 -8) cm 3 STP He cm -2 a -1 which supplements in situ produced He within the aquifer. Adoption of J0 values over this range lowers 4He residence times

  19. 14C chronology of the oldest Scandinavian church in use. An AMS/PIXE study of lime lump carbonate in the mortar

    International Nuclear Information System (INIS)

    Lindroos, Alf; Ranta, Heikki; 14C Dating Laboratory, Department of Physics and Astronomy, University of Aarhus (Denmark))" data-affiliation=" (AMS 14C Dating Laboratory, Department of Physics and Astronomy, University of Aarhus (Denmark))" >Heinemeier, Jan; Lill, Jan-Olof

    2014-01-01

    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 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 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 14 C age of the lime lumps of this particular church is an important contribution to the discussion on stone church chronology in Scandinavia

  20. {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.

  1. Processing behaviors of thin-film pentacene and benzene-1,4-diboronic acid in supercritical carbon dioxide

    International Nuclear Information System (INIS)

    Ngo, Truc T.; Keegan, James E.; George, Robert D.

    2011-01-01

    This research investigates the feasibility of using supercritical carbon dioxide (scCO 2 ) as a green solvent for processing organic thin film semiconductor, such as pentacene, and a potential molecular modifier for use in electronic device applications. Benzene-1,4-diboronic acid (BDBA) was selected as a molecular modifier in this work due to its electron deficient nature, which can potentially enhance pentacene's physical, chemical or electronic properties by changing its structure in the solid state. In this study, the solubilities of BDBA and pentacene in scCO 2 are measured as individual compounds and as co-solutes, at 313 K, using ultraviolet (UV) spectroscopy. Methanol co-solvent effects on solubility have also been characterized for each compound. The results show that BDBA is insoluble in pure scCO 2 up to 1.82 × 10 7 Pa. However, with a small amount of methanol added to the mixture, BDBA becomes soluble in solution with a solubility of 3.81 × 10 −4 mol/l at 9.00 × 10 6 -Pa-pressure. In contrast, pentacene is only soluble in scCO 2 at pressures above 1.10 × 10 7 Pa, and its solubility is decreased upon addition of methanol due to the non-polar nature of pentacene. When a pentacene thin film is treated with BDBA in scCO 2 /methanol solution, BDBA sorption is observed at pressures as low as 8.80 × 10 6 Pa. Based on these results, it is concluded that treatment of pentacene thin films in scCO 2 is a promising approach that can be optimized for BDBA and other similar molecular modifiers, to produce multi-component organic thin film devices.

  2. 14C fixation by leaves and leaf cell protoplasts of the submerged aquatic angiosperm Potamogeton lucens: Carbon dioxide or bicarbonate?

    International Nuclear Information System (INIS)

    Staal, M.; Elzenga, J.T.M.; Prins, H.B.A.

    1989-01-01

    Protoplasts were isolated from leaves of the aquatic angiosperm Potamogeton lucens L. The leaves utilize bicarbonate as a carbon source for photosynthesis, and show polarity; that is acidification of the periplasmic space of the lower, and alkalinization of the space near the upper leaf side. At present there are two models under consideration for this photosynthetic bicarbonate utilization process: conversion of bicarbonate into free carbon dioxide as a result of acidification and, second, a bicarbonate-proton symport across the plasma membrane. Carbon fixation of protoplasts was studied at different pH values and compared with that in leaf strips. Using the isotopic disequilibrium technique, it was established that carbon dioxide and not bicarbonate was the form in which DIC actually crossed the plasma membrane. It is concluded that there is probably no true bicarbonate transport system at the plasma membrane of these cells and that bicarbonate utilization in this species apparently rests on the conversion of bicarbonate into carbon dioxide. Experiments with acetazolamide, an inhibitor of periplasmic carbonic anhydrase, and direct measurements of carbonic anhydrase activity in intact leaves indicate that in this species the role of this enzyme for periplasmic conversion of bicarbonate into carbon dioxide is insignificant

  3. 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

  4. Immobilization of carbon-14 from reactor graphite waste by use of self-sustaining reaction in the C-Al-TiO2 system

    International Nuclear Information System (INIS)

    Karlina, O.K.; Klimov, V.L.; Ojovan, M.I.; Pavlova, G.Yu.; Dmitriev, S.A.; Yurchenko, A.Yu.

    2005-01-01

    As a result of long-term neutron irradiation, the long-lived 14 C is produced in the reactor graphite. The exothermic self-sustaining reaction 3C(graphite) + 4Al + 3TiO 2 = 3TiC + 2Al 2 O 3 was proposed for processing of such waste. In doing so, the carbon, including the 14 C, is chemically bound in the stable TiC. The reaction products in the C-Al-TiO 2 system were investigated both by thermodynamic simulation and experimentally in the course of this work

  5. 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...

  6. 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.

  7. Carbon-14 tracer studies in rat-liver perfusion experiments under conditions of gluconeogenesis from lactate and pyruvate

    International Nuclear Information System (INIS)

    Muellhofer, G.; Schwab, A.; Mueller, C.; Stetten, C. von; Gruber, E.

    1977-01-01

    The intracellular events in the metabolic pathway of gluconeogenesis from lactate and pyruvate in liver tissue were assumed to be understood. Nevertheless the results of several 14 C-tracer experiments gave rise to the postulation of still unknown intracellular interactions under this condition. A contribution was made to the solution of this problem by using different 14 C labelled tracers such as [1- 14 C]lactate or pyruvate and [2- 14 C]lactate or pyruvate. [ 14 C]bicarbonate and [1- 14 C]-octanoate in perfusion experiments with livers from rats under conditions of gluconeogenesis from lactate and pyruvate. The 14 C labelling patterns of intracellular metabolities such as malate, citrate, phosphoenolpyruvate, phosphoglycerate and newly synthesized glucose were analysed under different conditions. A comparison with values calculated by using metabolic models based on the generally accepted concepts of intracellular interactions showed some fundamental discrepancies which justify the postulation. (orig./MG) [de

  8. Constraints on primary and secondary particulate carbon sources using chemical tracer and 14C methods during CalNex-Bakersfield

    Data.gov (United States)

    U.S. Environmental Protection Agency — The present study investigates primary and secondary sources of organic carbon for Bakersfield, CA, USA as part of the 2010 CalNex study. The method used here...

  9. 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

    1997-12-31

    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.)

  10. 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.)

  11. Carbon-14 exchange between CO2 and CO in the system 14CO2-CO-NOsub(x)(Ar, N2, O2)-quartz vessels

    International Nuclear Information System (INIS)

    Wawer, A.; Zielinski, M.

    1981-01-01

    It has been established that the rate of 14 C exchange between CO 2 and CO is diminished in presence of NO and NO 2 . The temperature dependence of the overall rate of exchange and the partial orders in respect to separate components of the exchange mixtures have been determined. The rate dependence on quartz surface has been established and the surface mechanism considered. The inhibiting action NO and NO 2 is explained. At higher pressures the catalytic effect of NO was found and explained. (author)

  12. 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...... by microwave heating to afford [1-C-14]levulinic acid. Subsequently, bromination and oxidation gave the targeted furan-2-one with a radiochemical purity of > 97% and a specific activity of 57 mCi/mmol....

  13. Isotopic and chemical composition (δ13C, Δ14C, δ15N, C:N, SUVA254nm, % HPOA) of aquatic carbon and field conditions (water temperature, pH, discharge) in the Upper Mississippi River Basin, October 2014 – February 2016

    Data.gov (United States)

    Department of the Interior — This dataset contains stable isotope (δ13C) and radioisotope (Δ14C) compositions of dissolved inorganic carbon, dissolved organic carbon, particulate organic carbon,...

  14. Krypton-81, Helium-4 and Carbon-14 based estimation of groundwater ages in the Guarani Aquifer System: implications for the He-4 geochronometer

    Science.gov (United States)

    Aggarwal, P. K.; Chang, H. K.; Gastmans, D.; Sturchio, N. C.; Araguas, L.; Matsumoto, T.; Lu, Z.; Jiang, W.; Yokochi, R.; Mueller, P.

    2012-12-01

    Characterization of aquifer systems remains a challenge, particularly for large aquifers with limited hydrogeological information. Groundwater age is an important parameter that integrates aquifer recharge and flow dynamics and provides the ability to reliably constrain groundwater models. We have used multiple isotope tracers (C-14, He-4, and Kr-81) to estimate the age of groundwater along a 400-km transect in the north-eastern part of the Guarani Aquifer System (GAS) in Brazil. Carbon-14 measurements were made with an AMS, He-4 by mass-spectrometry, and Kr-81 by atom trap trace analysis (ATTA). Groundwater samples were collected along a groundwater flow path that runs from the outcrop area in the east to the deep confined section in the west, where the aquifer is up to about 1000 m deep. Present groundwater recharge occurs in the outcrop areas, as indicated by the presence of tritium and modern 14C. Carbon-14 activities reach values below detection limit at relatively short distances (a few km) from the outcrop. Abundance of 81Kr (half-life 229 Ka), in samples free of C-14, decreases from 0.81±0.11 (expressed as (81Kr/Kr)sample/(81Kr/Kr)air) in the east to 0.18±0.03 in the western-most sample (estimated age = 566±60 ka). Measured 4He-excess is far above that expected from in-situ production rates in sandstone aquifers and overestimates the age by several orders of magnitude. We used 81Kr ages to calibrate the 4He geochronometer which indicates a basal flux of about 2.8 x10-11 cm3STP He/cm2/a. This flux is lower than most estimates of basal flux in previous studies and will allow a wider use of 4He for groundwater dating and aquifer characterization.

  15. Synthesis of carbon-14 and tritium labeled cis-3,4-dichloro-N-methyl-N-[2-(1-pyrrolidinyl)cyclohexyl]benzamidehydrochloride, an anticonvulsant agent

    International Nuclear Information System (INIS)

    Hsi, R.S.P.; Stolle, W.T.; Ayer, D.E.

    1992-01-01

    The title compound, U-54494A, is an anticonvulsant agent with clinical potential for treating epilepsy and a broad spectrum of seizure disorders. Structurally it is related to kappa opiod agonists and shares their anticonvulsant properties, but appears to be devoid of analgesic, sedative, and diuretic side effects. It also has been shown to inhibit neuronal damage and seizures induced by excitatory amino acids. This report describes the synthesis of the racemic U-54494A labeled with carbon-14 at the carboxamide carbon and with tritium in the pyrrolidine ring at C-3 and C-4. These radioisotope labeled versions of U-54494A were prepared for conducting drug disposition studies of this compound in test animals and human subjects

  16. 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)

    Taylor, E.M.; Huckins, H.E.

    1995-01-01

    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

  17. 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).

  18. 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.

  19. Simulations of radiocarbon in a coarse-resolution world ocean model 2. Distributions of bomb-produced Carbon 14

    International Nuclear Information System (INIS)

    Toggweiler, J.R.; Dixon, K.; Bryan, K.

    1989-01-01

    Part 1 of this study examined the ability of the Geophysical Fluid Dynamics Laboratory (GFDL) primitive equation ocean general circulation model to simulate the steady state distribution of naturally produced 14 C in the ocean prior to the nuclear bomb tests of the 1950's and early 1960's. In part 2 begin with the steady state distributions of part 1 and subject the model to the pulse of elevated atmospheric 14 C concentrations observed since the 1950's

  20. Neutron-transmuted carbon-14 in neutron-irradiated GaN: Compensation of DX-like center

    International Nuclear Information System (INIS)

    Ida, T.; Oga, T.; Kuriyama, K.; Kushida, K.; Xu, Q.; Fukutani, S.

    2013-01-01

    The transmuted-C related luminescence and net carrier concentration are studied by combining photoluminescence, liquid scintillation, and Raman scattering. GaN single crystal films grown by metalorganic-vapor-phase epitaxy are irradiated with fast and thermal neutrons at fluxes of 3.9 × 10 13 cm −2 s −1 and 8.15 × 10 13 cm −2 s −1 , respectively. Irradiation time is 48 hours. The calculated 72 Ge and 14 C concentrations are 1.24 × 10 18 cm −3 and 1.13 × 10 18 cm −3 , respectively. The transmuted 14 C is detected by the liquid scintillation method to survey β-rays emitted in the process of 14 C decays from 14 N. Tritium ( 3 H) is also emitted by a (n,t) reaction of 14 N due to the neutron irradiation above 4.5 MeV. Photoluminescence relating to C, DX-like center of Ge and yellow luminescence band are observed in 1000 °C annealed NTD-GaN. The free electron concentration estimated from Raman scattering is 4.97 × 10 17 cm −3 . This value is lower than that from the transmuted Ge concentration, suggesting the compensation due to the transmuted 14 C acceptors

  1. Carbonization

    Energy Technology Data Exchange (ETDEWEB)

    Hennebutte, H G; Goutal, E

    1921-07-04

    Materials such as coal, peat, or schist are subjected to a rising temperature in successive stages in apparatus in which the distillation products are withdrawn at each stage. For example in a three-stage process, the acid products of the first or low-temperature stage are fixed in a suitable reagent, the basic products from a second or higher-temperature stage are absorbed in an acid reagent, hydrocarbons being retained by solvents, while the third are subjected to a pyrogenation process carried out in a closed vessel. Wherein the material is subjected in stages to a rising temperature, the gasified products being withdrawn at each stage, and are prevented as far as possible from mixing with the carbonized products.

  2. Production cross section measurement of discrete gammas-ray at 90 degree for interactions of 14. 9 MeV neutrons with carbon and niobium

    Energy Technology Data Exchange (ETDEWEB)

    Zhou Hongyu; Yan Yiming; Tang lin; Wen Chenlin; Zhang Shenji; Hua Ming; Han Chongzhan; Ding Xiaoji; Lan Liqiao; Fan Guoying; Yan Hua; Wang Xingfu; Wang Qi; Sun Suxu; Rong Yaning; Liu Shuzhen (Institute of Low Energy Nuclear Physics, Beijing Normal University, Beijing (CN))

    1989-05-01

    The cross sections of discrete gamma-ray produced by interactions of 14.9 MeV neutrons with carbon and niobium were investigated. A pulsed {ital T}({ital d},{ital n}){sup 4} He neutron source was used in the measurement. Neutron flux incident upon the sample was determined with the associated particle method. Technique of time-of-flight was used for reducing the background. A new method to calculate neutron flux attenuation in large cylindrical sample was proposed. The split of 4.439 MeV gamma-ray line from {sup 12}C({ital n},{ital n}{prime}{gamma}){sup 12}C reactions was confirmed. 79 discrete gamma-ray lines and their production cross sections for the interactions of 14.9 MeV neutrons with niobium were obtained for the first time.

  3. Non-elastic cross-sections for neutron interactions with carbon and oxygen above 14 MeV

    International Nuclear Information System (INIS)

    Brenner, D.J.; Prael, R.E.

    1985-01-01

    In the light of the new generation of high energy (less than or equal to 80 MeV) neutron therapy facilities currently being tested, the need for neutron kerma factors in the range from 15 to 80 MeV on carbon and oxygen has become of urgent importance. Not enough experimental data currently exist or are likely to be measured soon, so a nuclear model is essential for interpolation or, less satisfactorily, extrapolation of available data. The use of a suitable model, applicable to light nuclei, is shown to be crucial. Such a model is described, and good agreement between its results and the experimental data in the energy range of interest is reported. Comparisons between the model predictions and the ENDF/B-V evaluation of the non-elastic cross section for carbon between 15 and 20 MeV indicate that a re-evaluation of ENDF is required. 35 refs., 12 figs., 6 tabs

  4. 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)

    Winterfeld, Maria

    2014-08-01

    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 (δ 13 C and Δ 14 C) 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

  5. 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)

    Yunoki, Shunji; Saito, Masaaki; Nagakawa, Yoshiyasu

    2012-01-01

    The influence of atmospheric 14 CO 2 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 14 CO 2 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 14 CO 2 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 14 C 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 14 CO 2 decreased. We recommend that the influence of atmospheric 14 CO 2 should be corrected when fuel samples contain low amounts of 14 C. (author)

  6. 14C dating and stable carbon isotopes of soil organic matter in the Southeastern region of Sao Paulo State

    International Nuclear Information System (INIS)

    Mofatto, Milene; Pessenda, Luiz Carlos Ruiz; Bendassoli, Jose Albertino; Leite, Acacio Zuniga; Oliveira, Paulo de Oliveira; Garcia, Ricardo Jose Francischetti

    2005-01-01

    The objective of this research is to characterize the isotopic composition ( 13 C, 14 C) of soil organic matter (SOM) in the Parque Estadual da Serra do Mar-Nucleo Curucutu, Sao Paulo state, Southeastern Brazil. The isotopic composition (δ 13 C) of SOM will be used as an indicator of vegetation types from the local ecosystems and 14 C dating (humin fraction) used to determine the chronology. The results from SOM indicated vegetation changes in the last 10,000 years, where, a less dense vegetation occurred in the past, with C 3 plant predominant and/or a mixture of C 3 and C 4 . (author)

  7. Impact of Different Types of Activated Carbon on the Bioaccessibility of 14C-phenanthrene in Sterile and Non-Sterile Soils

    Directory of Open Access Journals (Sweden)

    Ayodeji Oyelami

    2014-10-01

    Full Text Available In this study, the impact of three different types of activated carbon (AC on the bioaccessibility of 14C-phenanthrene in non-sterile and sterile soils was investigated. A single dose (1% of each of the different AC (CB4, CP1 and AQ5000 was blended with soil spiked with 50 mg·kg−1 of 12C/14C-phenanthrene. The mineralisation of the 14C-phenanthrene was monitored over a 14 day incubation period by indigenous soil microflora and an enriched inoculum of Pseudomonas sp., while uptake in earthworms, Eisenia fetida, was measured after incubation for 10 days at 1, 25, 50 and 100 d. Bioaccessibility was assessed using hydroxypropyl-β-cyclodextrin (HPCD solution. Results showed that the presence of AC had a significant effect upon the extents of mineralisation, earthworm uptake and HPCD extraction, when compared to the control. Aquasorb CB4 was the least effective amongst the different AC used. The characteristics of the different AC used was also seen to have a major influence on how each AC would have an effect on its use in soil remediation in reducing bioaccessibility, mobility and risk.

  8. Micro-syntheses for the use of carbon 13 or carbon 14. Micro-preparations of methyl alcohol, methyl iodide, and sodium acetate labeled in the methyl group

    International Nuclear Information System (INIS)

    Baret, C.; Pichat, L.

    1951-11-01

    Apparatus and technique are described in detail for (1) reduction of CO 2 to CH 3 OH with LiAlH 4 , (2) conversion of the methanol to CH 3 I by HI, (3) formation of the Mg Grignard reagent, and (4) addition of inactive CO 2 to form CH 3 COOH. All these operations have been carried out on 0.005 moles. Methyl-labeled Na acetate has been prepared in 67% yield based on the Ba 14 CO 3 used as starting material. (author) [fr

  9. Syntheses of {gamma}-aminobutyric-1-{sup 14}C and of {alpha}-aminoadipic-6-{sup 14}C acid from methoxy-3 chloropropyl-magnesium and marked carbon dioxide; Syntheses de l'acide {gamma}-aminobutyrique{sup 14}C-1 et de l'acide {alpha}-aminoadipique {sup 14}C-6 a partir de methoxy-3 chloropropylmagnesium et d'anhydride carbonique marque

    Energy Technology Data Exchange (ETDEWEB)

    Liem, Phung Nhu [Commissariat a l' Energie Atomique, Saclay (France). Centre d' Etudes Nucleaires, Departement des radioelements, Service des molecules marquees

    1967-04-01

    Carbonation of {gamma}-methoxypropyl-magnesium chloride by CO{sub 2} gives {gamma}-methoxy-butyric carboxylic-{sup 14}C acid with a yield of about 95 per cent. When the latter is treated successively with anhydrous HBr and with diazomethane, methyl carboxylic {gamma}-bromobutyrate-{sup 14}C is formed. This in turn gives {gamma}-amino-butyric carboxylic-{sup 14}C acid with an overall yield of 66 per cent with respect to Ba{sup 14}CO{sub 3}, when it is condensed with potassium phthalimide and hydrolyzed by acid. By reacting methyl-{gamma}-bromobutyrate-{sup 14}C with the sodium derivative of ethyl cyanacetamido-acetate in ethanol, followed by an acid hydrolysis, {alpha}-aminoadipic-6-{sup 14}C acid is obtained with an overall yield of 46 per cent with respect to Ba{sup 14}CO{sub 3}. (author) [French] La carbonatation du chlorure de {gamma}-methoxypropylmagnesium par {sup 14}CO{sub 2} donne l'acide {gamma}-methoxybutyrique carboxyle {sup 14}C avec un rendement d'environ 95 pour cent. Ce dernier traite successivement par HBr anhydre et par le diazomethane conduit au {gamma}-bromobutyrate de methyle carboxyle {sup 14}C. Celui-ci condense avec le phtalimide de potassium suivi d'une hydrolyse acide fournit l'acide {gamma}-aminobutyrique carboxyle {sup 14}C avec un rendement global de 66 pour cent par rapport a Ba{sup 14}CO{sub 3}. L'action du {gamma}-bromobutyrate de methyle {sup 14}C sur le derive sode du cyanacetamidoacetate d'ethyle dans l'ethanol suivie d'hydrolyse acide donne l'acide {alpha}-aminoadipique {sup 14}C-6 avec un rendement global de 46 pour cent par rapport a Ba{sup 14}CO{sub 3}. (auteur)

  10. Determination of water, hydrogen, and carbon content of Korean main farm produces for the calculation of H-3 and C-14 ingestion dose

    International Nuclear Information System (INIS)

    Chung, Yang Geun; Lee, Gab Bock; Kim, Mi Ja; Eum, Hee Moon

    2003-01-01

    Water, hydrogen, and carbon content of grains, leafy vegetable, root vegetable, and fruits in Korea were determined to be used in the calculation of HTO, OBT, C-14 offsite ingestion dose. The individual items and the weighting factors of the 4 groups were based on the results of nationwide dietary intake survey in Korea. Items produced in an island or imported were excluded for the reason that they would not be affected directly by the nuclear power plants in the nation. On the same assumption, cooked and instant foods also were excluded. Items within 95% of the cumulative percentage of intake in each category were selected as the main farm produces, and then each intake percentage was taken as the weighting factor. Water, Hydrogen, and carbon content were determined using the data in Food Composition TABLE of Korea. H and C content were calculated from protein, fat, and carbohydrate content in the TABLE, and multiplied by each weighting factor to make the group-representative value. Grains, lefty and root vegetable, and fruits of Korea had 11.0%, 93.6%, 87.9%, 86.2% of water, 5.6%, 0.4%. 0.7%, 0.9% of hydrogen, and 39.6%, 2.5%, 5.2%, 6.0% of carbon, respectively. This is different from those in the ODCM from AECL data. Over ODCM, water content of grains and vegetable were 0.92-0.98 times ODCM, and fruits 1.03 times ODCM, which would result in the change of HTO ingestion dose as much. Hydrogen content of grains and vegetables are 1.02-2.33 times ODCM, but fruits 0.9 times ODCM. Carbon content of grains, leafy vegetables, and fruits are 0.7-0.98 times ODCM, but root vegetables 1.49 times ODCM. This would result in the change of ingestion dose as much

  11. Use of 14C as tracer in studies of distribution of the carbon in the plant/soil system

    International Nuclear Information System (INIS)

    Eduardo, B.P.; Cerri, C.C.

    1989-01-01

    A short time experiment with 14 C labelling, in which two-month-old sugar cane plants photosynthetically assimilated 14 CO 2 was carried out in greenhouse conditions. Data on distribution of synthesized metabolites were obtained. Although the results are referred only to dynamic conditions, which change during the vegetative cycle, it is possible to state that during this phase an important part of the metabolites go to underground compartment of the system, with considerable lose due to root respiration and rhizo-deposition. The accuracy of the technique is a good evidence of its usefulness in studies of energy transference, both within the plant and in interspecific comparisons. Longer and/or more intense labelling, associated with a longer stabilization period of the metabolites might help in studies of humification of rhizo-depositions in soil. (author)

  12. Carbon-14-ochratoxin A distribution in the Japanese quail (Coturnix coturnix japonica) monitored by whole body autoradiography

    International Nuclear Information System (INIS)

    Fuchs, R.; Appelgren, L.E.; Hagelberg, S.; Hult, K.

    1988-01-01

    Tissue distribution of the nephrotoxic mycotoxin ochratoxin A was characterized in laying Japanese quail by whole body autoradiography and scintillation counting using 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

  13. Characterization of diverse soybean genotypes using 14 carbon for organic acid exudation under phosphorus stress and its relationship with phosphorus acquisition efficiency

    International Nuclear Information System (INIS)

    Vengavasi, Krishnapriya; Pandey, Renu

    2017-01-01

    To characterise the physiological aspects influencing organic acid exudation under low phosphorus (P) stress, experiment was conducted to screen a diverse soybean panel (comprising 116 genotypes) for total carbon exudation employing shoot labelling with 14 CO 2 technique. Among the traits measured at seedling stage, total carbon ( 14 C) exudation, P uptake and total dry weight contributed to the maximum genotypic variability in soybean. The proportion of organic acids (including oxalate, citrate, succinate and fumarate) was the highest among root-exuded compounds induced by low P stress in soybean. Improved root length, surface area and volume coupled with higher activity of enzymes in TCA cycle contributed to enhanced organic acid exudation under low P. Efficient soybean genotypes (EC-232019 and G-2344) exhibited superior growth and P acquisition efficiency under low soil P availability attributed to its higher root exudation potential aiding in mining fixed soil P. To understand the molecular mechanism differentially regulating root exudation potential in contrasting genotypes (EC-232019 and EC-113396), root proteome analysis at low P stress was carried out. Among the total proteins visualised by 2D-gel electrophoresis, 105 genotypes (32%) were differentially expressed between sufficient and low P levels. A total of 44 (14%) proteins were down-regulated by more than two-fold while 61 (15%) proteins were up-regulated by more than two-fold at low P. The differential proteins were involved in a myriad of functions including organic acid accumulation, carbohydrate, protein and lipid metabolism under low P stress. Characterisation of 17 proteins with unknown function indicated the role of novel genes under low P stress. The identified genotypes have potential to be used as donors in crop improvement programs to develop high-yielding P-efficient cultivars which may be an asset to low-input sustainable agriculture. (author)

  14. Ba(OH)2.8H2O process for the removal and immobilization of carbon-14. Final report

    International Nuclear Information System (INIS)

    Haag, G.L.; Holladay, D.W.; Pitt, W.W. Jr.; Young, G.C.

    1986-01-01

    The airborne release of 14 C from various nuclear facilities has been identified as a potential biohazard due to the long half-life of 14 C (5730 years) and the ease with which it may be assimilated into the biosphere. At ORNL, technology has been developed for the removal and immobilization of this radionuclide. Prior studies have indicated that 14 C will likely exist in the oxidized form as CO 2 and will contribute slightly to the bulk CO 2 concentration of the gas stream, which is air-like in nature (approx.300 ppM/sub v/ CO 2 ). The technology that has been developed utilizes the CO 2 -Ba(OH) 2 .8H 2 O gas-solid reaction with the mode of gas-solid contacting being a fixed bed. The product, BaCO 3 , possesses excellent thermal and chemical stability, prerequisites for the long-term disposal of nuclear wastes. For optimal process operation, studies have indicated that an operating window of adequate size does exist. When operating within the window, high CO 2 removal efficiency (effluent concentrations 99%), and an acceptable pressure drop across the bed (3 kPa/m at a superficial velocity of 13 cm/s) are possible. Three areas of experimental investigation are reported: (1) microscale studies on 150-mg samples to provide information concerning surface properties, kinetics, and equilibrium vapor pressures; (2) macroscale studies on large fixed beds (4.2 kg of reactant) to determine the effects of humidity, temperature, and gas flow rate upon bed pressure drop and CO 2 breakthrough; and (3) design, construction, and operation of a pilot unit capable of continuously processing a 34-m 3 /h (20-ft 3 /min) air-based gas stream

  15. Electrochemical Behaviour of Tinidazole at 1,4-Benzoquinone Modified Carbon Paste Electrode and Its Direct Determination in Pharmaceutical Tablets and Urine by Differential Pulse Voltammetry

    Directory of Open Access Journals (Sweden)

    Yosef Nikodimos

    2017-01-01

    Full Text Available A simple and highly sensitive electrochemical method based on a 1,4-benzoquinone modified carbon paste electrode (1,4-BQMCPE was described for the determination of tinidazole (TDZ. In Britton Robinson buffer solution, TDZ yields well-defined irreversible reduction peak at −0.344 V on a 1,4-BQMCPE. Compared with that on a bare CPE, the reduction peak of TDZ increased significantly on the modified CPE and the effects of different parameters on the voltammetric responses were also investigated. Differential pulse voltammetric method was proposed and optimized for TDZ determination and its reductive peak current response at 1,4-BQMCPE was found to show linear dependence on the concentration of TDZ in the range of 1.0 × 10−6 to 5.0 × 10−4 M with a linear regression equation, correlation coefficient, limit of detection (LOD, and limit of quantification (LOQ of IPC (μA = 0.19958 + 0.02657C (μM, 0.99486, 1.10 × 10−7 M, and 3.77 × 10−7, respectively. Excellent recovery results for spiked TDZ in pharmaceutical tablet samples ranging within 97.44–97.51% and in urine ranging within 95.37–96.91% were observed. The selectivity of the method for TDZ was further studied in the presence of selected potential interferents and confirmed the potential applicability of the developed method for the determination of TDZ.

  16. Permafrost Organic Carbon Mobilization From the Watershed to the Colville River Delta: Evidence From 14C Ramped Pyrolysis and Lignin Biomarkers

    Science.gov (United States)

    Zhang, Xiaowen; Bianchi, Thomas S.; Cui, Xingqian; Rosenheim, Brad E.; Ping, Chien-Lu; Hanna, Andrea J. M.; Kanevskiy, Mikhail; Schreiner, Kathryn M.; Allison, Mead A.

    2017-11-01

    The deposition of terrestrial-derived permafrost particulate organic carbon (POC) has been recorded in major Arctic river deltas. However, associated transport pathways of permafrost POC from the watershed to the coast have not been well constrained. Here we utilized a combination of ramped pyrolysis-oxidation radiocarbon analysis (RPO 14C) along with lignin biomarkers, to track the linkages between soils and river and delta sediments. Surface and deep soils showed distinct RPO thermographs which may be related to degradation and organo-mineral interaction. Soil material in the bed load of the river channel was mostly derived from deep old permafrost. Both surface and deep soils were transported and deposited to the coast. Hydrodynamic sorting and barrier island protection played important roles in terrestrial-derived permafrost POC deposition near the coast. On a large scale, ice processes (e.g., ice gauging and strudel scour) and ocean currents controlled the transport and distribution of permafrost POC on the Beaufort Shelf.

  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)

    Paula Eduardo, B.J.F. de.

    1987-01-01

    The flow of carbon in three different crops, maize, beans and sugar cane was studied by use of 14 V. 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) [pt

  18. Incorporation of /sup 14/C glucose into glycogen and glucose-6-phosphate dehydrogenase activity in rat brain following carbon monoxide intoxication

    Energy Technology Data Exchange (ETDEWEB)

    Sikorska, M; Gorzkowski, B; Szumanska, G; Smialek, M [Polska Akademia Nauk, Warsaw. Centrum Medycyny Doswiadczalnej i Klinicznej; Panstwowy Zaklad Higieny, Warsaw (Poland))

    1975-01-01

    Incorporation of /sup 14/C glucose into glycogen and glucose-6-phosphate dehydrogenase activity in rat brain following carbon monoxide intoxication was studied. In brains of rats tested on the 20, 30 and 60th minute of exposure to CO and immediately after removal from the chamber the enzyme activity showed no essential deviation from the control level. In the group of rats tested 1 hour after taking them out from the chamber increase of the enzyme activity was noticed, amounting to about 33% of the control value. The brains tested 24 hours after exposure showed the largest increase of the enzyme activity by about 94%. In the next time periods, 48 and 72 hours after intoxication, the enzyme activity was decreasing. The glycogen content in brains of control animals increased 3 hours after CO intoxication by about 69%. The increase of glycogen synthesis was expressed by increase of the total radioactivity, which amounted to 160% of the control value.

  19. Electrocatalytic determination of L-ascorbic acid by modified glassy carbon with Ni(Me2(CH3CO)2[14]tetraenoN4) complex.

    Science.gov (United States)

    Khorasani-Motlagh, Mozhgan; Noroozifar, Meissam

    2003-12-01

    A novel modified glassy carbon electrode containing Ni(Me2(CH3CO)2[14]tetraenoN4) complex was used as an electrocatalytic sensor for the determination of L-ascorbic acid in pH = 6.6. The peak potential shifted to negative by 205 mV compared with that for a bare electrode in cyclic voltammograms. The calibration curve was linear up to 6.2 x 10(-3) M with a detection limit 3.1 x 10(-7) M and an RSD% better than 2.47%. This newly modified electrode was applied to commercial pharmaceutical tablets, injections and foods. The obtained results were identical to those obtained by the classical 2,6-dichlorophenolindophenol method.

  20. Comparative dual-tracer studies of carbon-14 tryptophan and iodine-131 HIPDM in animal models of pancreatic diseases

    International Nuclear Information System (INIS)

    Kubota, K.; Som, P.; Brill, A.B.; Sacker, D.F.; Meinken, G.E.; Srivastava, S.C.; Atkins, H.L.

    1989-01-01

    Our previous studies have shown that a significant amount of the diamine derivative 131 I-N,N,N'-trimethyl-N'-(2-hydroxy-3-methyl-5-iodobenzyl)-1,3- propanediamine (HIPDM) is taken up and retained by the normal pancreas. Therefore, we studied the uptake of [ 13 1I]HIPDM in various pathophysiological models in mice (chronic alcoholism, diabetes with beta-cell atrophy and obesity with beta-cell hypertrophy) and compared to 14 C-L-Tryptophan (TRY) distribution in order to determine the factors influencing their pancreatic uptake. In normal animals, the pancreas uptake of TRY was generally higher than HIPDM. In diabetes, the relative concentration of both compounds was higher over the controls; however, in obesity, TRY showed lower accumulation than in controls while HIPDM showed no significant difference. Chronic ethanol (20%) ingestion increased TRY uptake in the pancreas compared to controls (36.88 ± 3.21 vs. 30.03 ± 4.17% ID/g; p less than 0.01) after 5 wk study period, but it decreased by 10 wk (22.36 ± 0.95% ID/g; p less than 0.005). There were no significant changes in [ 131 I]HIPDM distribution in alcoholics as compared to the controls. Radioiodinated HIPDM has potential advantages over [ 11 C]TRY for pancreatic imaging since conventional imaging techniques can be employed. Our data, however, suggest that 11 C-L-TRY is a more sensitive indicator of various pancreatic disorders

  1. Accuracy of a rapid 10-minute carbon-14 urea breath test for the diagnosis of Helicobacter pylori-associated peptic ulcer disease

    Energy Technology Data Exchange (ETDEWEB)

    Chiahung, Kao [Taichung Veterans General Hospital (Taiwan, Province of China). Dept. of Nuclear Medicine; Shyhjen, Wang [Taichung Veterans General Hospital (Taiwan, Province of China). Dept. of Nuclear Medicine; Chungyuan, Hsu [Taichung Veterans General Hospital (Taiwan, Province of China). Dept. of Nuclear Medicine; Wanyu, Lin [Taichung Veterans General Hospital (Taiwan, Province of China). Dept. of Nuclear Medicine; Chihkua, Huang [Taichung Veterans General Hospital (Taiwan, Province of China). Dept. of Gastroenterology; Granhum, Chen [Taichung Veterans General Hospital (Taiwan, Province of China). Dept. of Gastroenterology

    1993-08-01

    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 [mu]Ci of carbon-14 labelled urea. For each patient only one breath sample was collected in hyamine at 10 min. The amount of [sup 14]C collected at 10 min was expressed as follows: (DPM/mmol CO[sub 2] 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 [sup 14]C-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.)

  2. 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)

    Kao Chiahung; Wang Shyhjen; Hsu Chungyuan; Lin Wanyu; Huang Chihkua; Chen Granhum

    1993-01-01

    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 14 C collected at 10 min was expressed as follows: [(DPM/mmol CO 2 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 14 C-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.)

  3. 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

    Energy Technology Data Exchange (ETDEWEB)

    Payne, L., E-mail: liam.payne@bristol.ac.uk [Interface Analysis Centre, HH Wills Physics Laboratory, University of Bristol, BS8 1TL (United Kingdom); Walker, S.; Bond, G. [Centre for Materials Science, University of Central Lancashire, PR1 2HE (United Kingdom); Eccles, H. [John Tyndall Institute for Nuclear Research, School of Computing, Engineering and Physical Sciences, University of Central Lancashire, PR1 2HE (United Kingdom); Heard, P.J.; Scott, T.B. [Interface Analysis Centre, HH Wills Physics Laboratory, University of Bristol, BS8 1TL (United Kingdom); Williams, S.J. [Radioactive Waste Management, B587, Curie Avenue, Harwell Oxford, Didcot, OX11 0RH (United Kingdom)

    2016-03-15

    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 {sup 14}C 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 {sup 14}C-containing deposits on some irradiated Magnox reactor graphite.

  4. Down-regulation of KORRIGAN-like endo-β-1,4-glucanase genes impacts carbon partitioning, mycorrhizal colonization and biomass production in Populus

    Directory of Open Access Journals (Sweden)

    Udaya C Kalluri

    2016-10-01

    Full Text Available A greater understanding of the genetic regulation of plant cell wall remodeling and the impact of modified cell walls on plant performance is important for the development of sustainable biofuel crops. Here, we studied the impact of down-regulating KORRIGAN-like cell wall biosynthesis genes, belonging to the endo-β-1,4-glucanase gene family, on Populus growth, metabolism and the ability to interact with symbiotic microbes. The reductions in cellulose content and lignin syringyl-to-guaiacyl unit ratio, and increase in cellulose crystallinity of cell walls of PdKOR RNAi plants corroborated the functional role of PdKOR in cell wall biosynthesis. Altered metabolism and reduced growth characteristics of RNAi plants revealed new implications on carbon allocation and partitioning. The distinctive metabolome phenotype comprised of a higher phenolic and salicylic acid content, and reduced lignin, shikimic acid and maleic acid content relative to control. Plant sustainability implications of modified cell walls on beneficial plant-microbe interactions were explored via co-culture with an ectomycorrhizal fungus, Laccaria bicolor. A significant increase in the mycorrhization rate was observed in transgenic plants, leading to measurable beneficial growth effects. These findings present new evidence for functional interconnectedness of cellulose biosynthesis pathway, metabolism and mycorrhizal association in plants, and further emphasize the consideration of the sustainability implications of plant trait improvement efforts.

  5. COFFEE, TEA AND SUGAR-SWEETENED CARBONATED SOFT DRINK INTAKE AND PANCREATIC CANCER RISK: A POOLED ANALYSIS OF 14 COHORT STUDIES

    Science.gov (United States)

    Genkinger, Jeanine M.; Li, Ruifeng; Spiegelman, Donna; Anderson, Kristin E.; Albanes, Demetrius; Bergkvist, Leif; Bernstein, Leslie; Black, Amanda; van den Brandt, Piet A.; English, Dallas R.; Freudenheim, Jo L.; Fuchs, Charles S.; Giles, Graham G.; Giovannucci, Edward; Goldbohm, R. Alexandra; Horn-Ross, Pamela L.; Jacobs, Eric J.; Koushik, Anita; Männistö, Satu; Marshall, James R.; Miller, Anthony B.; Patel, Alpa V.; Robien, Kim; z, Thomas E.; Schairer, Catherine; Stolzenberg-Solomon, Rachael; Wolk, Alicja; Ziegler, Regina G.; Smith-Warner, Stephanie A.

    2011-01-01

    BACKGROUND Coffee has been hypothesized to have pro- and anti-carcinogenic properties, while tea may contain anti-carcinogenic compounds. Studies assessing coffee intake and pancreatic cancer risk have yielded mixed results, while findings for tea intake have mostly been null. Sugar-sweetened carbonated soft drink (abbreviated as SSB) intake has been associated with higher circulating levels of insulin, which may promote carcinogenesis. Few prospective studies have examined SSB intake and pancreatic cancer risk; results have been heterogeneous. METHODS In this pooled analysis from 14 prospective cohort studies, 2,185 incident pancreatic cancer cases were identified among 853,894 individuals during follow-up. Multivariate (MV) study-specific relative risks (RR) and 95% confidence intervals (CI) were calculated using Cox proportional hazards models and then pooled using a random effects model. RESULTS No statistically significant associations were observed between pancreatic cancer risk and intake of coffee (MVRR=1.10, 95% CI=0.81-1.48 comparing ≥900 to 0.05). These associations were consistent across levels of sex, smoking status and body mass index. When modeled as a continuous variable, a positive association was evident for SSB (MVRR=1.06, 95% CI=1.02-1.12). CONCLUSION AND IMPACT Overall, no associations were observed for intakes of coffee or tea during adulthood and pancreatic cancer risk. Although we were only able to examine modest intake of SSB, there was a suggestive, modest positive association for risk of pancreatic cancer for intakes of SSB. PMID:22194529

  6. Imaging and retention measurements of selenium 75 homocholic acid conjugated with taurine, and the carbon 14 glycochol breath test to document ileal dysfunction due to late radiation damage

    International Nuclear Information System (INIS)

    Valdes Olmos, R.; Hartog Jager, F. den; Hoefnagel, C.; Taal, B.; Netherlands Cancer Inst., Amsterdam

    1991-01-01

    In order to assess ileal dysfunction in patients with complaints after pelvic radiation therapy, retention measurements and scintigraphic imaging with selenium 75 homocholic acid conjugated with taurine ( 75 Se-HCAT), combined with the carbon 14 clycochol breath test, were evaluated in 39 patients. In 22 patients without ileal resection the results of the 75 Se-HCAT test and the breath test differentiated between a normal functioning ileum (both tests negative) and ileal dysfunction as a cause of complaints (one or both tests positive). Among the patients with ileal dysfunction, the combination of both tests permitted those with bacterial overgrowth (breath test positive, 75 Se-HCAT negative) to be separated from patients with evidence of bile acid malabsorption ( 75 Se-HCAT positive, breath test positive or negative). In 17 patients with small-bowel resection, the 75 Se-HCAT test helped to estimate the severity of bile acid malabsorption with implications for therapy. In this group the breath test was false-negative in 7 cases with abnormal 75 Se-HCAT. Additional systematically performed scintigraphic imaging improved the accuracy of the 75 Se-HCAT test, revealing cases with prolonged colonic accumulation of the radiopharmaceutical, causing spurious retention values. In conclusion, assessment of ileal dysfunction by nuclear medicine techniques in post-irradiation conditions provides information about the aetiology and therefore the possibility of adjustment in the clinical management. (orig.)

  7. Preparation of C{sup 14}-labelled tetrazolium salts and tracer study of the tetrazene-formazan rearrangement; Preparation de sels de tetrazolium marques au carbone-14 et etude de la transposition tetrazene-formazan, au moyen d'indicateurs radioactifs; Izgotovlenie mechennykh C{sup 14} solej tetrazosoedinenij i issledovanie pri pomoshchi indikatorov peregruppirovok tetrazona-formazana; Preparacion de sales de tetrazolio marcadas con {sup 14}C y estudio de la transposicion tetraceno-formazan con ayuda de trazadores

    Energy Technology Data Exchange (ETDEWEB)

    Marton, Joseph; Meisel, Julia [Central Research Institute for Chemistry of the Hungarian Academy of Sciences, Budapest (Hungary); Gosztonyi, Thomas [Institute of Organic Chemical Technology, Technical University, Budapest (Hungary)

    1962-03-15

    The preparation of [5-C{sup 14}]-TTC, [5, 5'-di-C{sup 14}]NT (neotetrazolium) and [5, 5'-di-C{sup 14}]-BT (tetrazolium blue) starting from benzaldehyde- [1-C{sup 14}] has been accomplished. The yields for both mono- and ditetrazolium salts are high, and the products can be obtained with high sp. activity. The purity of the samples was investigated by paper chromatography. In the case of ditetrazolium salts some impurities could be detected and conclusions drawn as to their structure and quantity. A method has been developed to prepare C{sup 14}- labelled ditetrazolium salts of high purity. The formation of the formazan, the precursor of the tetrazolium salt, goes through an unstable intermediate of tetrazene-type structure which rearranges rapidly in basic medium, to yield the formazan. The tetrazene intermediate can be isolated under suitable conditions. By using C{sup 14}-labelled benzaldehyde phenylhydrazone this rearrangement was investigated and a verification of its intramolecular character given. (author) [French] On a procede a la preparation de [5-C{sup 14}]-TTC, de [5,5'-di-C{sup 14}] NT (neotetrazolium) et de [5,5'-di-C{sup 14}]-VT (bleu de tetrazolium), en partant du benzaldehyde-[1-C{sup 14}]. On a pu obtenir un grand rendement, tant pour les sels de monotetrazolium que pour les sels de ditetrazolium, et des produits d'une activite specifique elevee. La purete des echantillons a ete examinee par chromatographie sur papier. Dans le cas des sels de ditetrazolium, on a pu deceler quelques impuretes et tirer des conclusions quant a leur structure et quantite. On a mis au point une methode permettant de preparer des sels de ditetrazolium marques au carbone-14 et presentant une grande purete. Dans la synthese du formazan, precurseur du sel de tetrazolium, on obtient un produit intermediaire instable d'une structure analogue a celle du tetrazene; ce produit se transforme rapidement en milieu alcalin pour donner du formazan. Le tetrazene intermediaire peut

  8. Dissolved inorganic carbon, alkalinity, temperature and salinity collected from discrete sample and profile observations using CTD, bottle and other instruments from G. M. DANNEVIG in the Skagerrak from 2012-01-14 to 2012-01-14 (NCEI Accession 0157321)

    Data.gov (United States)

    National Oceanic and Atmospheric Administration, Department of Commerce — NCEI Accession 0157321 includes chemical, discrete sample, physical and profile data collected from G. M. DANNEVIG in the Skagerrak from 2012-01-14 to 2012-01-14....

  9. Assessing the Resilience of a Blue Carbon Store: Characterizing the Lateral Flux of DIC from an East Coast U.S. Saltmarsh using Δ14C and δ13C

    Science.gov (United States)

    Felgate, S. L.; Gonneea, M. E.; Kroeger, K. D.; Chu, S. N.; Wang, A. Z.

    2016-12-01

    Intertidal saltmarshes are highly productive coastal habitats and important blue carbon stores. They commonly exhibit high salinity, low oxygen environmental regimes which lend themselves towards reduced rates of microbial respiration, and the assimilation of atmospheric CO2 into plant biomass tends to outpace the rate at which that biomass is broken down. As a result, a relatively high proportion of CO2 entering the system can be expected to become incorporated into marsh sediment before it can be metabolised, potentially entering storage for thousands of years and providing a sizeable natural carbon sink. However, the rate at which these habitats are now being degraded is substantial and growing: the combined impacts of stressors such as increasing temperature and sea level rise are predicted to reduce global saltmarsh coverage by 30-40% by the end of the century, and many saltmarsh carbon stores can be expected to shift from net sinks to sources within the same time frame. Based on high resolution measurements and modelling in a northeastern U.S. saltmarsh, a recent study reported a marsh DIC export of 414g C m2 yr-1. This is more than twice that put forward in previous estimates, and is larger than the total uptake by plant biomass. This translates into one of the largest carbon fluxes to the coastal ocean found along the U.S. East Coast. Additionally it is possible that the marsh carbon budget is not in balance, with export exceeding carbon fixation rates. Here we characterise this carbon flux using Δ14C and δ13C data to age and source the exported dissolved carbon pools. Carbon isotope mixing models between surface (modern) and porewater (old) carbon sources are constrained by creek samples and porewaters from multiple depths and locations within the marsh. We determine the age of exported carbon to see if carbon stored over the lifetime of the marsh (c. 2000 years) continues to be respired, thereby evaluating the long term resilience of the carbon sink.

  10. Decomposition performance of animals as an indicator of stress acting on beech-forest ecosystems - microcosmos experiments with carbon-14-labelled litter components

    International Nuclear Information System (INIS)

    Schaefer, M.; Wolters, V.

    1988-01-01

    The effect of acid rain and heavy metals on the biotic interactions in the soil of beech forest with mull, must, and limed must was investigated with the aid of close-to-nature microcosmos systems. Parameters made use of were the decomposition of carbon-14-labelled litter components and the turnover of the microflora in C, N, and P. As the results show, increased proton uptake will bear on rearly every stage of the decomposition process in mull soils. As a result, there may be litter accumulation on the ground and first signs of humus disintegration in the mineral soil of mull soils. A direct relation between the acidity of the environment and the extent of decomposition inhibition does not exist. Despite wide-ranging impairment of edaphic animals, the activity of the ground fauna still is to be considered as the most important buffer system of soils rich in bases. Acidic condition of the beech forest soils with the humus form 'must' led to drastic inhibition of litter decomposition, to a change of the effect of edaphic animals, and to an increase in N mineralization. The grazing animals frequently aggravate the decomposition inhibition resulting from acid precipitation. The comparision of the decomposition process in a soil containing must as compared to one containing mull showed acidic soils to be on a lower biological buffer level than soils rich in bases. The main buffer capacity of acidic soils lies in the microflora, which is adapted to sudden increases in acidity and which recovers quickly. In the opinion of the authors, simple liming is not enough to increase the long-term biogenic stability of a forest ecosystem. A stabilizing effect of the fauna, for instance on nitrogen storage, is possible only if forest care measuries are carried out, for instance careful loosening of the mineral soil, which will attract earthworm species penetrating deeply into the soil. (orig./MG) With 12 refs., 6 figs [de

  11. Removal of Legacy Low-Level Waste Reactor Moderator De-ionizer Resins Highly Contaminated with Carbon-14 from the 'Waste with no Path to Disposal List' Through Innovative Technical Analysis and Performance Assessment Techniques

    International Nuclear Information System (INIS)

    Goldston, W.T.; Hiergesell, R.A.; Kaplan, D.I.; Pope, H.L.

    2006-01-01

    At the Savannah River Site (SRS), nuclear production reactors used de-ionizers to control the chemistry of the reactor moderator during their operation to produce nuclear materials primarily for the weapons program. These de-ionizers were removed from the reactors and stored as a legacy waste and due to the relatively high carbon-14 (C-14) contamination (i.e., on the order of 740 giga becquerel (GBq) (20 curies) per de-ionizer) were considered a legacy 'waste with no path to disposal'. Considerable progress has been made in consideration of a disposal path for the legacy reactor de-ionizers. Presently, 48 - 50 de-ionizers being stored at SRS have 'no path to disposal' because the disposal limit for C-14 in the SRS's low-level waste disposal facility's Intermediate Level Vault (ILV) is only 160 GBq (4.2 curies) per vault. The current C-14 ILV disposal limit is based on a very conservative analysis of the air pathway. The paper will describe the alternatives that were investigated that resulted in the selection of a route to pursue. This paper will then describe SRS's efforts to reduce the conservatism in the analysis, which resulted in a significantly larger C-14 disposal limit. The work consisted of refining the gas-phase analysis to simulate the migration of C-14 from the waste to the ground surface and evaluated the efficacy of carbonate chemistry in cementitious environment of the ILV for suppressing the volatilization of C-14. During the past year, a Special Analysis was prepared for Department of Energy approval to incorporate the results of these activities that increased the C-14 disposal limits for the ILV, thus allowing for disposal of the Reactor Moderator De-ionizers. Once the Special Analysis is approved by DOE, the actual disposal would be dependent on priority and funding, but the de-ionizers will be removed from the 'waste with no path to disposal list'. (authors)

  12. The preparation of nucleotides uniformly labelled with carbon-14 by biosynthetic methods. Isolation of adenylic, uridylic, cytidylic,and guanylic acids, from the alkaline hydrolysate of escherichia coli RNA

    International Nuclear Information System (INIS)

    Garcia Pineda, M. D.; Pacheco Lopez, J.

    1978-01-01

    A method is described for the preparation and analysis of adenylic, uri dilic, cytidi- 11c and guanylic acids, labelled with 14 C . Escherichia coli cells have been labelled by growing them in a medi dia containing glucose-14 C as their only source of carbon. RNA is isolated from the cells, and after hydrolysis of the molecule the resulting nucleotides are separated by gel filtration and exchange chromatography. Chemical and radiochemical purity of the Isolated nucleotides is determined, and also its specific radioactivity. (Author) 30 refs

  13. Thermodynamic and kinetic studies of the equilibration reaction between the sulfur and carbon bonded forms of a cobalt(III) complex with the ligands 1,4,7-triazycyclononane and 1,4-diaza-7-thiacyclodecane

    DEFF Research Database (Denmark)

    Song, Y.S.; Becker, J.; Kofod, Pauli

    1996-01-01

    The new cyclic thioether 1,4-diaza-7-thiacyclodecane, dathicd, has been synthesized and used for the prepn. of the sulfur- and carbon-bonded cobalt(III) complexes: [Co(tacn)(S-dathicd)]Cl3.5H2O and [Co(tacn)(C-dathicd)](ClO4)2 (tacn, 1,4,7-triazacyclononane; C-dathicd, 1,4-diamino-7-thiacyclodecan......-sulfur complex to form the alkyl complex gave 100% loss of deuterium. It is concluded that the labile methylene proton is bound to the carbon atom which in the alkyl complex is bound to cobalt(III). From the kinetic data it is estd. that the carbanion reacts with water 270 times faster than it is captured...

  14. The fate of river organic carbon in coastal areas: A study in the Rhône River delta using multiple isotopic (δ13C, Δ14C) and organic tracers

    Science.gov (United States)

    Cathalot, C.; Rabouille, C.; Tisnérat-Laborde, N.; Toussaint, F.; Kerhervé, P.; Buscail, R.; Loftis, K.; Sun, M.-Y.; Tronczynski, J.; Azoury, S.; Lansard, B.; Treignier, C.; Pastor, L.; Tesi, T.

    2013-10-01

    A significant fraction of the global carbon flux to the ocean occurs in River-dominated Ocean Margins (RiOMar) although large uncertainties remain in the cycle of organic matter (OM) in these systems. In particular, the OM sources and residence time have not been well clarified. Surface (0-1 cm) and sub-surface (3-4 cm) sediments and water column particles (bottom and intermediate depth) from the Rhône River delta system were collected in June 2005 and in April 2007 for a multi-proxy study. Lignin phenols, black carbon (BC), proto-kerogen/BC mixture, polycyclic aromatic hydrocarbons (PAHs), carbon stable isotope (δ13COC), and radiocarbon measurements (Δ14COC) were carried out to characterize the source of sedimentary organic material and to address degradation and transport processes. The bulk OM in the prodelta sediment appears to have a predominantly modern terrigenous origin with a significant contribution of modern vascular C3 plant detritus (Δ14COC = 27.9‰, δ13COC = -27.4‰). In contrast, the adjacent continental shelf, below the river plume, seems to be dominated by aged OM (Δ14COC = -400‰, δ13COC = -24.2‰), and shows no evidence of dilution and/or replacement by freshly produced marine carbon. Our data suggest an important contribution of black carbon (50% of OC) in the continental shelf sediments. Selective degradation processes occur along the main dispersal sediment system, promoting the loss of a modern terrestrial OM but also proto-kerogen-like OM. In addition, we hypothesize that during the transport across the shelf, a long term resuspension/deposition loop induces efficient long term degradation processes able to rework such refractory-like material until the OC is protected by the mineral matrix of particles.

  15. On the isolation of elemental carbon (EC) for micro-molar 14C accelerator mass spectrometry: development of a hybrid reference material for 14C-EC accuracy assurance, and a critical evaluation of the thermal optical kinetic (TOK) EC isolation procedure

    Science.gov (United States)

    Currie, L. A.; Kessler, J. D.

    2005-10-01

    The primary objective of the research reported here has been the development of a hybrid reference material (RM) to serve as a test of accuracy for elemental carbon (EC) isotopic (14C) speciation measurements. Such measurements are vital 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 (char) from SRM 1515 in the EC isolate of the Hybrid RM, as well as a test for conservation of its dominant soot fraction throughout the isolation procedure. The secondary objective was to employ the Hybrid RM for the comparative evaluation of the thermal optical kinetic (TOK) and thermal optical transmission (TOT) methods for the isolation of EC for micro-molar carbon accelerator mass spectrometry (AMS). As part of this process, the relatively new TOK method was subjected to a critical evaluation and significant development. Key findings of our study are: (1) both methods exhibited biomass-C "leakage"; for TOT, the EC fraction isolated for AMS contained about 8% of the original biomass-C; for TOK, the refractory carbon (RC) isolated contained about 3% of the original biomass-C.; (2) the initial isothermal oxidation stage of

  16. On the isolation of elemental carbon (EC for micro-molar 14C accelerator mass spectrometry: development of a hybrid reference material for 14C-EC accuracy assurance, and a critical evaluation of the thermal optical kinetic (TOK EC isolation procedure

    Directory of Open Access Journals (Sweden)

    L. A. Currie

    2005-01-01

    Full Text Available The primary objective of the research reported here has been the development of a hybrid reference material (RM to serve as a test of accuracy for elemental carbon (EC isotopic (14C speciation measurements. Such measurements are vital 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 (char from SRM 1515 in the EC isolate of the Hybrid RM, as well as a test for conservation of its dominant soot fraction throughout the isolation procedure. The secondary objective was to employ the Hybrid RM for the comparative evaluation of the thermal optical kinetic (TOK and thermal optical transmission (TOT methods for the isolation of EC for micro-molar carbon accelerator mass spectrometry (AMS. As part of this process, the relatively new TOK method was subjected to a critical evaluation and significant development. Key findings of our study are: (1 both methods exhibited biomass-C 'leakage'; for TOT, the EC fraction isolated for AMS contained about 8% of the original biomass-C; for TOK, the refractory carbon (RC isolated contained about 3% of the original biomass-C.; (2 the initial isothermal oxidation stage

  17. The preparation of nucleotides uniformly labelled with carbon-14 by biosynthetic methods. Isolation of adenylic, uridylic, cytidylic,and guanylic acids, from the alkaline hydrolysate of escherichia coli RNA; Preparacion de nucleiotidos uniformemente marcados con 14{sup C}, por via biosintetica. Aislamiento de los acidos adenilico, uridilico, citidilico y guanilico, procedentes de la hidrolisis alcalina de RNA de escherichia Coli.

    Energy Technology Data Exchange (ETDEWEB)

    Garcia Pineda, M D; Pacheco Lopez, J

    1978-07-01

    A method is described for the preparation and analysis of adenylic, uri dilic, cytidi- 11c and guanylic acids, labelled with 14{sup C}. Escherichia coli cells have been labelled by growing them in a medi dia containing glucose-14{sup C} as their only source of carbon. RNA is isolated from the cells, and after hydrolysis of the molecule the resulting nucleotides are separated by gel filtration and exchange chromatography. Chemical and radiochemical purity of the Isolated nucleotides is determined, and also its specific radioactivity. (Author) 30 refs.

  18. A study of the mechanism of certain heterogeneous catalytic processes using C{sup 14}-labelled compounds; Utilisation de composes marques au carbone-14 pour l'etude du mecanisme de certains processus catalytiques heterogenes; Issledovanie mekhanizma nekotorykh geterogenno-kataliticheskikh protsessov s primeneniem soedinenij, mechennykh uglerodom-14; Estudio del mecanismo de algunos procesos de catalisis heterogenea con ayuda de compuestos marcados con carbono-14

    Energy Technology Data Exchange (ETDEWEB)

    Isagulyants, G V; Balandin, A A

    1962-03-15

    An investigation is made of the method of calculating individual phase velocities for parallel, consecutive and parallel-consecutive reactions from kinetic data obtained by the use of labelled atoms. The method is used for calculating individual phase velocities in the decomposition reaction of isopropyl alcohol into vanadium trioxides, dehydrogenations of butane-butylene mixtures and dehydrations of ethyl alcohol. Compounds containing C{sup 14} were used in this study. (author) [French] Le memoire expose une methode par laquelle on calcule les vitesses a differents stades dans les reactions paralleles, consecutives et paralleles-consecutives en se servant de donnees cinetiques obtenues par l'utilisation d'atomes indicateurs. Cette methode est utilisee pour le calcul des vitesses a differents stades de la decomposition de l'alcool isopropylique par le trioxyde de vanadium, de la deshydrogenation des melanges butane-butylene et de la deshydratation de l'alcool ethylique. Pour ces travaux, on a utilise des composes contenant du carbone-14. (author) [Spanish] Se describe un metodo de calculo de las velocidades correspondientes a las distintas etapas de una serie de reacciones paralelas, consecutivas y paralelo-consecutivas, partiendo de datos cineticos obtenidos mediante atomos marcados. El metodo se aplica a la determinacion de las velocidades de las reacciones de descomposicion del alcohol isopropilico por el trioxido de vanadio, de deshidrogenacion de mezclas de butano y buteno y de deshidratacion del alcohol etilico. El trabajo se llevo a cabo con ayuda de compuestos marcados con carbono-14. (author) [Russian] Rassmotren metod rascheta skorostej otdel'nykh stadij dlya parallel'nykh, konsekutivnykh i parallel'no-konsekutivnykh reaktsij, iskhodya iz kineticheskikh dannykh, poluchennykh s primeneniem mechenykh atomov. Metod primenen k raschetu skorostej otdel'nykh stadij v reaktsii razlozheniya izopropilovogo spirta na trekhokisi vanadiya, degidrogenizatsii butan

  19. Carbon-14 activity of fallout in Araucaria angustifolia annual growth rings, from Arapoti, Parana State, Brazil; Atividade de {sup 14} C do 'fallout' em aneis anuais de crescimento de Araucaria angustifolia, de Arapoti - PR

    Energy Technology Data Exchange (ETDEWEB)

    Lisi, Claudio Sergio; Pessenda, Luiz Carlos Ruiz [Centro de Energia Nuclear na Agricultura (CENA), Piracicaba, SP (Brazil). Lab. de 14 C; Tomazello Filho, Mario [Escola Superior de Agricultura Luiz de Queiroz, Piracicaba, SP (Brazil). Dept. de Ciencias Florestais. Lab. de Dendrocronologia

    2000-07-01

    During the period of nuclear tests between 1950 and 1960, an input of artificial {sup 14} C (fallout effect) occurred in the natural reservoirs. {sup 14} C determinations in the Northern Hemisphere showed values of {delta}{sup 14} C up to 960 in the year of 1964. To determine the fallout {sup 14} C activity in Brazil, wood samples from Araucaria angustifolia (Bert.) O. Kuntze, Araucariaceae, were collected in Arapoti-PR (24 deg 11{sup S}, 49 deg 58{sup O}). The annual tree rings were selected by dendrochronology. The cellulose was extracted and its {sup 14} C activity determined by liquid scintillation method. The results showed a significant increase of the {delta} {sup 14} C up to 590 in 1965, about 60% higher than the natural activity, gradually decreasing after the end of nuclear tests. These results were correlated with those obtained in the Northen Hemisphere and will be used in the studies of CO{sub 2} mechanisms distribuition to the atmosphere and other natural reservoirs. (author)

  20. Increased accuracy of the carbon-14 D-xylose breath test in detecting small-intestinal bacterial overgrowth by correction with the gastric emptying rate

    International Nuclear Information System (INIS)

    Chang Chisen; Chen Granhum; Kao Chiahung; Wang Shyhjen; Peng Shihnen; Huang Chihkuen; Poon Sekkwong

    1995-01-01

    The aim of this study was to determine whether the accuracy of 14 C-D-xylose breath test for detecting bacterial overgrowth can be increased by correction with the gastric emptying rate of 14 C-D-xylose. Ten culture-positive patients and ten culture-negative controls were included in the study. Small-intestinal aspirates for bacteriological culture were obtained endoscopically. A liquid-phase gastric emptying study was performed simultaneously to assess the amount of 14 C-D-xylose that entered the small intestine. The results of the percentage of expired 14 CO 2 at 30 min were corrected with the amount of 14 C-D-xylose that entered the small intestine. There were six patients in the culture-positive group with a 14 CO 2 concentration above the normal limit. Three out of four patients with initially negative results using the uncorrected method proved to be positive after correction. All these three patients had prolonged gastric emptying of 14 C-D-xylose. When compared with cultures of small-intestine aspirates, the sensitivity and specificity of the uncorrected 14 C-D-xylose breath test were 60% and 90%, respectively. In contrast, the sensitivity and specificity of the corrected 14 C-D-xylose breath test improved to 90% and 100%, respectively. (orig./MG)

  1. Soil and vegetation dynamics in a forest-savannah boundary in Southern Amazon state during the holocene, using 14C dating and stable carbon isotopes of soil organic matter

    International Nuclear Information System (INIS)

    Vidotto, Elaine; Pessenda, Luiz Carlos Ruiz; Ribeiro, Adauto de Souza; Bendassolli, Jose Albertino

    2005-01-01

    This work presents a comparative study between organic soil horizons formed in depressions, distant ca. 500 meters from each sampling site, in a forest/savannah boundary in the Southern Amazon Basin. The influence of the paleovegetation and soil dynamics, based on carbon isotope ( 12 C, 13 C, 14 C) data of soil organic matter (SOM) was evaluated. The soils were classified as Dystropept (Cambissolo) and were considered as clayey. The total organic carbon contents decreased from the surface to deeper parts of the soils profiles. At deeper parts of the soil profiles in the savannah site, between 100 cm and 30 cm, the δ 13 C values characterized the influence of C 4 plants (around -18,0 per mille). From about 20 cm to the surface the δ 13 C values characterized the mixture of C 3 and C 4 plants. The soil δ 13 C values in the forest site ranged from -25,0 per mille at deeper parts of the profile to -26,0 per mille in the surface, characterizing the dominance of C 3 plants in this location. 13 C and 14 C data from soil samples indicated a predominance of C 3 plants in the early Holocene. From ca. 7000 to 3000 years BP the influence of C 4 plants increased, characterizing a savannah expansion probably related to a drier climate in the region. Since 3000 years 14 C BP, the carbon isotope data suggest the forest expansion, probably due to a return to wetter climate. 14 C data in the 40-50 cm and 100 cm soil depth were contemporary, showing no difference on the soil organic matter deposition in the savannah and in the forest locations. (author)

  2. Carbon-14 studies on the role of oxygen-containing compounds in the reaction mechanism of the Fischer-Tropsch synthesis

    International Nuclear Information System (INIS)

    Aksoy, H.A.

    1975-01-01

    In this work the behaviour of organic oxygen compounds has been studied in the reaction mechanism of Fischer-Tropsch synthesis using the tracer method. As an oxygen carrying tracer materials i-propanole (2- 14 C), acetone (2- 14 C) and ethanole (1- 14 C) have been added to the synthesis gas. The synthesis experiments are performed under standard conditions: The synthesis products are separated in suitable fractions and then studied by gas- and radio-gaschromatography. As a result the C-number distributions of the synthesis products are obtained as a function of concentration (weight %, mol %) and radioactivity (activity %). On this basis the relative molar activities have been calculated for certain compounds and fractions. Adding i-propanole- 14 C a great part of the tracer compound is transformed to acetone- 14 C, however adding acetone- 14 C to the synthesis gas a large amount of i-propanole- 14 C is produced. The main hydrocarbon reaction product from i-propanol and acetone is propane. Besides propane also propene is produced with equal molar radioactivity. This indicates that the formation of adsorbed oxygen compounds, as they may also be produced by chemisorption from alcohols or carbonyle compounds, is the first step in the formation of hydrocarbons by hydrogenolytic separation of oxygen. Comparing the results obtained with ethanole- 14 C and i-propanole- 14 C as a tacer material, for ethane an essentially lower molar activity is obtained when adding ethanole- 14 C compared with propane when adding i-propanole- 14 C. This corresponds with a particularly low desorption probability at the C 2 -hydrocarbon level. (orig./HK) [de

  3. Free allocations in EU ETS Phase 3: The impact of emissions performance benchmarking for carbon-intensive industry - Working Paper No. 2013-14

    International Nuclear Information System (INIS)

    Lecourt, S.; Palliere, C.; Sartor, O.

    2013-02-01

    From Phase 3 (2013-20) of the European Union Emissions Trading Scheme, carbon-intensive industrial emitters will receive free allocations based on harmonised, EU-wide benchmarks. This paper analyses the impacts of these new rules on allocations to key energy-intensive sectors across Europe. It explores an original dataset that combines recent data from the National Implementing Measures of 20 EU Member States with the Community Independent Transaction Log and other EU documents. The analysis reveals that free allocations to benchmarked sectors will be reduced significantly compared to Phase 2 (2008-12). This reduction should both increase public revenues from carbon auctions and has the potential to enhance the economic efficiency of the carbon market. The analysis also shows that changes in allocation vary mostly across installations within countries, raising the possibility that the carbon-cost competitiveness impacts may be more intense within rather than across countries. Lastly, the analysis finds evidence that the new benchmarking rules will, as intended, reward installations with better emissions performance and will improve harmonisation of free allocations in the EU ETS by reducing differences in allocation levels across countries with similar carbon intensities of production. (authors)

  4. Carbon-14 tracer studies in the metabolism of isolated rat-liver parenchymal cells under conditions of gluconeogenesis from lactate and pyruvate

    International Nuclear Information System (INIS)

    Muellhofer, G.; Mueller, C.; Stetten, C. von; Gruber, E.

    1977-01-01

    In rat liver perfusion experiments under conditions of gluconeogenesis from lactate and pyruvate, 14 C-labeling patterns of metabolites with (1- 14 C)-labeled and (2- 14 C)-labeled lactate or pyruvate. [ 14 C]bicarbonate and [1- 14 C]octanoate as tracers have been obtained which do not agree with generally assumed reaction schemes. The experiments have been repeated with incubations of isolated rat-liver parenchymal cells. The results demonstrate that the discrepancies between expected and analysed 14 C-labeling patterns of metabolites were still existent. From this observation, it may be concluded that 14 C-labelling patterns of metabolites are indicative for the existence of still unknown metabolic relationships in liver parenchymal cells. Furthermore, the results of our experiments prove that conclusions based on the exclusive analysis of metabolite levels are of limited value for studying intracellular events, because of uncharacterized compartmentations, which become evident in 14 C-tracer studies. It cannot be answered by our studies whether the apparent existence of differently labelled species of citrate, oxoglutarate, or acetyl-CoA represent intracellular compartmentation, or whether it is the result of metabolic heterogeneity of liver parenchym cells. (orig.) [de

  5. Radiocarbon (14C) Concentration of Local Pollution in Street Trees Located at Intersections

    OpenAIRE

    Ogawa, Daisuke

    2018-01-01

    At large intersections, vehicles consume and generate a large amount of fossil fuel. Carbon derived from fossil fuels that do not contain radioactive carbon (14C), i.e., dead carbon, is released in large amounts in the roadside air environment. By means of photosynthesis, street trees along the roadside assimilate both dead carbon, not containing radioactive carbon (14C), and contemporary carbon, which includes radioactive carbon (14C). Therefore, the concentration of radioactive carbon (14C)...

  6. Solubility of methane and carbon dioxide in ethylene glycol at pressures up to 14 MPa and temperatures ranging from (303 to 423) K

    International Nuclear Information System (INIS)

    Galvao, A.C.; Francesconi, A.Z.

    2010-01-01

    This work reports solubility data of methane and carbon dioxide in ethylene glycol and the Henry's law constant of each solute in the studied solvent at saturation pressure. The measurements were performed at (303, 323, 373, 398, and 423.15) K and pressures up to 6.3 MPa for mixtures containing carbon dioxide and pressures up to 13.7 MPa for mixtures containing methane. The experiments were performed in an autoclave type phase equilibrium apparatus using the total pressure method (synthetic method). All investigated systems show an increase of gas solubility with the increase of pressure. A decrease of carbon dioxide solubility with the increase of temperature and an increase of methane solubility with the increase of temperature was observed. From the variation of solubility with temperature, the partial molar enthalpy, and entropy change are calculated.

  7. Transfer of carbon from 14C-labeled volatile fatty acids to other metabolites in the rumen epithelial slices of cattle

    International Nuclear Information System (INIS)

    Shoji, Yoshio; Tsuda, Tsuneyuki

    1979-01-01

    Incorporation of 1- 14 C-acetate, 1- 14 C-propionate and 1- 14 C-butyrate into various metabolite fractions in incubated bovine rumen epithelial slices was investigated in vitro. After 3 hours of in vitro incubation, the metabolites were fractionated into CO 2 , total organic acid, total lipid, non-lipid and residual fractions, and some of these fractions were fractionated further. 1- 14 C-acetate was less oxidized than 1- 14 C-propionate and 1- 14 C-butyrate in both Krebs-Ringer phosphate (KRP) and Krebs-Ringer bicarbonate (KRB) buffer solutions, and the oxidation rate of 1- 14 C-propionate was markedly higher in the KRB buffer than in the KRP buffer. As for organic acids examined, 1- 14 C-acetate was mainly incorporated into lactic, β-hydroxybutyric and pyruvic acids, 1- 14 C-propionate into lactic and succinic acids, and 1- 14 C-butyrate into β-hydroxybutyric and lactic acids, though substantial portions of all 3 volatile fatty acids (VFA) were incorporated into some other organic acids. Interconversion among these VFA was also observed in small amounts. Considerable amounts of these VFA were incorporated into lipid fraction, mainly into phospho-lipids and free higher fatty acids, and considerable amounts into some other lipids. About 10% of these 3 VFA added as substrates were incorporated into non-lipid fraction, mainly into the neutral fraction, but none of them into the cation fraction (amino acid fraction). Less than 1% of these 3 VFA were incorporated into the residual fraction which was considered to be tissue protein. (Kaihara, S.)

  8. Simplified analytical methods for the measurement of the synthesis rate of plasma proteins in vivo by the (/sup 14/C)carbonate method

    Energy Technology Data Exchange (ETDEWEB)

    Caine, S [Glasgow Royal Infirmary (UK); Fleck, A [Charing Cross Hospital, London (UK). Medical School

    1984-09-01

    A method is described for obtaining the specific activity of /sup 14/C in urea, essential in the measurement of the synthesis rate of a plasma protein in vivo, which is simpler than the original procedure. The principle is the measurement of /sup 14/CO/sub 2/ and NH/sub 4//sup +/ separately, after incubation with urease. A simple alteration gives samples of /sup 13/CO/sub 2/ for mass spectrometry. The 'recoveries' of /sup 14/C and /sup 13/C in urea were invariably between 90 and 96% and the CV was 3%.

  9. 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

    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 (δ{sup 13}C and Δ{sup 14}C) 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

  10. Lengths of Schwabe cycles in the seventh and eighth centuries indicated by precise measurement of carbon-14 content in tree rings

    Science.gov (United States)

    Miyake, Fusa; Masuda, Kimiaki; Nakamura, Toshio

    2013-12-01

    (14C) is produced in the atmosphere by galactic cosmic rays, which are modulated by solar magnetic activity. Its content in tree rings is retained and provides a record of past cosmic ray intensity and solar activity. We have measured, with 2 year resolution, the 14C content in Japanese cedar tree rings for the period A.D. 600 to 760, which includes a small grand solar minimum in the seventh to eighth centuries. Periodicity analysis of the 14C data shows that there is a component in the frequency band of the Schwabe cycle, with a period of 12-13 years continuing throughout the minimum. This is the fourth case in which an increase in the length of the Schwabe cycle has been observed in a grand solar minimum, after the Maunder Minimum, the Spörer Minimum, and the Fourth Century B.C. Minimum.

  11. Simultaneous determination of local cerebral glucose utilization and blood flow by carbon-14 double-label autoradiography: method of procedure and validation studies in the rat

    International Nuclear Information System (INIS)

    Ginsberg, M.D.; Smith, D.W.; Wachtel, M.S.; Gonzalez-Carvajal, M.; Busto, R.

    1986-01-01

    Validation studies were undertaken to establish a computer-assisted double-label autoradiographic strategy employing [ 14 C]2-deoxyglucose ([ 14 C]2DG) and [ 14 C]iodoantipyrine ([ 14 C]IAP) to measure local CMRglu (LCMRglu) and CBF (LCBF). An organic solvent was used to extract the majority of IAP between first and second film exposures. In contrast to previously published data, all solvents tested produced partial losses of 2DG from tissue, and all allowed 2-6% of IAP to persist even after 5-day washes. Technical-grade chloroform permitted equal retention of unmetabolized and metabolized 2DG. A linear model was established, which was insensitive to the changes in tissue self-absorption that were shown to occur with chloroform extraction. Propagated error in computing tissue [ 14 C]2DG and [ 14 C]IAP was reduced by maximizing IAP extraction (by longer solvent wash times) and by administering 2.5 times as much IAP as 2DG. Fractional 2DG retention was measured in single-label 2DG sections placed on the films, and fractional IAP retention was evaluated by an optimization procedure. With this strategy, double-label values for LCMRglu and LCBF in anesthetized rats agreed with values obtained in matched single-label series to within 5%. The coefficients of variation for the double- and single-label LCMRglu data were virtually identical, whereas the coefficient of variation for double-label LCBF was 1.8 times that of single-label LCBF. The double-label strategy permitted pixel-by-pixel measurement and video display of the LCMRglu/LCBF ratio; the mean value among structures was 0.472 mumol/ml. With proper attention to methodological detail, this double-label strategy shows great promise for routine laboratory application

  12. Performance of 2000CA/LL and 2260XL liquid scintillation spectrometers for low-level tritium and carbon-14 analyses

    International Nuclear Information System (INIS)

    Rozanski, K.; Stichler, W.; Schwarz, P.

    1991-01-01

    The performance of two commercially available liquid scintillation spectrometers for low-level counting of 3 H and 14 C has been investigated. Two models of new technology Tri-Carb spectrometers from the Packard Instrument Company were tested: the 2000CA/LL and 2260XL. The measurements revealed a superior 3 H performance of the 2000CA/LL equipment owing to its substantially higher counting efficiency. Results for 14 C are less conclusive and depend on the configuration of the counting parameters selected. A comparison of three commercially available scintillation cocktails for tritium assay in water samples revealed a superior performance for PicoFluor LLT. (Author)

  13. The Path of Carbon in Photosynthesis XIII. pH Effects in C{sup 14}O{sub 2} Fixation by Scenedesmus

    Science.gov (United States)

    Ouellet, C.; Benson, A. A.

    1951-10-23

    The rates of photosynthesis and dark fixation of C{sup 14}O{sub 2} in Scenedesmus have been compared in dilute phosphate buffers of 1.6 to 11.4 pH; determination of C{sup 14} incorporation into the various products shows enhancement of uptake in an acid medium into sucrose, polysaccharides, alanine and serine, in an alkaline medium into malic asparctic acids. kinetic experiments at extreme pH values suggest that several paths are available for CO{sub 2} assimilation. A tentative correlation of the results with the pH optima of some enzymes and resultant effects upon concentrations of intermediates is presented.

  14. Preparation of a Lipopolysaccharide from Escherichia coli 01lla, 01llb, k58: h21 bacterial wall, labeled with carbon-14

    International Nuclear Information System (INIS)

    Solano Aunon, M. L.; Pacheco Lopez, J.; Garcia Pineda, M. D.; Roca, M.; Bayon, A.

    1981-01-01

    A brief description of the morphological and chemical structure of Li po polysaccharides is given, as well as its occurrence in nature and its mechanisms of action. It is emphasized the usefulness for actual biochemical and biomedical research of the labeled Lipopolysaccharide. The method for the labelling, isolation and purification of 14''C-Lipopolysacchari de is described. (Author) 23 refs

  15. Biodegradation of Poly(butylene succinate Powder in a Controlled Compost at 58 °C Evaluated by Naturally-Occurring Carbon 14 Amounts in Evolved CO2 Based on the ISO 14855-2 Method

    Directory of Open Access Journals (Sweden)

    Masahiro Funabashi

    2009-09-01

    Full Text Available The biodegradabilities of poly(butylene succinate (PBS powders in a controlled compost at 58 °C have been studied using a Microbial Oxidative Degradation Analyzer (MODA based on the ISO 14855-2 method, entitled “Determination of the ultimate aerobic biodegradability of plastic materials under controlled composting conditions—Method by analysis of evolved carbon dioxide—Part 2: Gravimetric measurement of carbon dioxide evolved in a laboratory-scale test”. The evolved CO2 was trapped by an additional aqueous Ba(OH2 solution. The trapped BaCO3 was transformed into graphite via a serial vaporization and reduction reaction using a gas-tight tube and vacuum manifold system. This graphite was analyzed by accelerated mass spectrometry (AMS to determine the percent modern carbon [pMC (sample] based on the 14C radiocarbon concentration. By using the theory that pMC (sample was the sum of the pMC (compost (109.87% and pMC (PBS (0% as the respective ratio in the determined period, the CO2 (respiration was calculated from only one reaction vessel. It was found that the biodegradabilities determined by the CO2 amount from PBS in the sample vessel were about 30% lower than those based on the ISO method. These differences between the ISO and AMS methods are caused by the fact that part of the carbons from PBS are changed into metabolites by the microorganisms in the compost, and not changed into CO2.

  16. 2-Butyne-1,4-diol as a novel corrosion inhibitor for API X65 steel pipeline in carbonate/bicarbonate solution

    Energy Technology Data Exchange (ETDEWEB)

    Sadeghi Meresht, E. [Materials Engineering Department, Faculty of Engineering, Tarbiat Modares University, 1411713114, Tehran (Iran, Islamic Republic of); Shahrabi Farahani, T., E-mail: tshahrabi34@modares.ac.ir [Materials Engineering Department, Faculty of Engineering, Tarbiat Modares University, 1411713114, Tehran (Iran, Islamic Republic of); Neshati, J. [Research Institute of Petroleum Industry, RIPI, 1485733111, Tehran (Iran, Islamic Republic of)

    2012-01-15

    Highlights: Black-Right-Pointing-Pointer Corrosion of API 5L X65 is effectively reduced by the addition of the inhibitor. Black-Right-Pointing-Pointer The techniques include weight loss, potentiodynamic polarization, EIS and AFM. Black-Right-Pointing-Pointer 2-Butyne-1,4-diol acts as a mixed-type inhibitor. Black-Right-Pointing-Pointer The adsorption of 2-butyne-1,4-diol obeys Langmuir adsorption isotherm. - Abstract: The inhibition effects of 2-butyne-1,4-diol on the corrosion susceptibility of grade API 5L X65 steel pipeline in 2 M Na{sub 2}CO{sub 3}/1 M NaHCO{sub 3} solution were studied by electrochemical techniques and weight loss measurements. The results indicated that this inhibitor was a mixed-type inhibitor, with a maximum percentage inhibition efficiency of approximately 92% in the presence of 5 mM inhibitor. Atomic force microscopy revealed that a protective film was formed on the surface of the inhibited sample. The adsorption of the inhibitor was found to conform to the Langmuir isotherm with the standard adsorption free energy of -21.08 kJ mol{sup -1}.

  17. 2-Butyne-1,4-diol as a novel corrosion inhibitor for API X65 steel pipeline in carbonate/bicarbonate solution

    International Nuclear Information System (INIS)

    Sadeghi Meresht, E.; Shahrabi Farahani, T.; Neshati, J.

    2012-01-01

    Highlights: ► Corrosion of API 5L X65 is effectively reduced by the addition of the inhibitor. ► The techniques include weight loss, potentiodynamic polarization, EIS and AFM. ► 2-Butyne-1,4-diol acts as a mixed-type inhibitor. ► The adsorption of 2-butyne-1,4-diol obeys Langmuir adsorption isotherm. - Abstract: The inhibition effects of 2-butyne-1,4-diol on the corrosion susceptibility of grade API 5L X65 steel pipeline in 2 M Na 2 CO 3 /1 M NaHCO 3 solution were studied by electrochemical techniques and weight loss measurements. The results indicated that this inhibitor was a mixed-type inhibitor, with a maximum percentage inhibition efficiency of approximately 92% in the presence of 5 mM inhibitor. Atomic force microscopy revealed that a protective film was formed on the surface of the inhibited sample. The adsorption of the inhibitor was found to conform to the Langmuir isotherm with the standard adsorption free energy of −21.08 kJ mol −1 .

  18. Carbon-14 and Hydrogen-3 Measurement by Means of a Liquid Scintillation Spectrometer: Colour Quenching; Mesure du Carbone-14 et du Tritium a l'Aide d'un Spectrometre a Scintillateurliquide: Extinction Chromatique; Izmerenie soderzhaniya Ugleroda-14 i Vodoroda-3 s pomoshch'yu zhidkostnogo stsintillyatsionnogo spektrometra. oslablenie tsveta; Influencia de la Extincion Cromatica en la Medicion del Carbono-14 y del Hidrogeno-3 por Espectrometria del Centelleo Liquido

    Energy Technology Data Exchange (ETDEWEB)

    Iwakura, T.; Kasida, Y. [National Institute of Radiological Sciences, Chiba (Japan)

    1965-10-15

    An attempt was made to correlate colour quenching and wavelength of the absorption maximum in liquid scintillators. Attempts were also made to find a difference in discriminator ratio versus counting efficiency curves between chemical and colour quenching. Fourteen photosensitive cyanine dyes were used as colouring agents in alcohol solution. The concentration of the dye in the counting samples ranged from 0.5 to 10 x 10{sup -6} M to give the desired absorbance in the liquid scintillator medium. Toluene-1-{sup 14}C and toluene-{sup 3}H were used as the internal standards. Counting was carried out with a Packard TRI-CARB Model 314 EX2 liquid scintillation spectrometer. Discriminator settings were 100-1000 divisions for the red channel and 186-1000 divisions fox the green channel. The high voltage applied to the photomultiplier was selected to give balance point operation in the red channel in an unquenched sample. Concentration of dyes against extent of quenching was examined. Because of the characteristic wavelengths of light emitted by the scintillator systems and the response of the photomultipliers (S-11 response), it was expected that red and yellow solutions which have maximum absorption at 400-500 nm would show the greatest quenching effect. To evaluate the total colour quenching, the following relationship was used to define the total absorption coefficient: A = ({Sigma}A{sub i}W{sub i})/({Sigma}W{sub i}) where W{sub i} is the relative photomultiplier sensitivity for light within the spectral range i nm, and A{sub i} is the absorbance of light within the spectral range i nm used. Total absorbance was calculated for each 40 nm range. 360-400, 400-440 etc., to 520-560 nm. The reciprocal absorbance 1/A versus the counting efficiency shows a linear relationship over a wide range of counting efficiencies. The curves of the discriminator ratio versus counting efficiency show that when colour quenching becomes strong, the colour quenching curve separates from the

  19. Effect of aldicarb on growth and radio-carbon (/sup 14/C) and radio-phosphorus (/sup 32/P) assimilation by Rhizobium japonicum

    Energy Technology Data Exchange (ETDEWEB)

    Balasubramanian, A; Nilakantan, G [University of Agricultural Sciences, Bangalore (India). Radiotracer Lab.

    1976-01-01

    In vitro studies on the effect of aldicarb (2-methyl-2-(methyl thio) propionaldehde-o-methyl carbamoyl oxime), a soil applied systemic insecticide, on Rhizobium japonicum revealed that the chemical (at 1,2 and 5 ppm levels) stimulated the growth of the organism initially upto 48 hr which declined thereafter upto 72 hr. The incorporation of /sup 14/C-glucose by the cells considerably reduced due to the insecticide treatment. The production of extracellular, water-soluble slime (polysacchardes) was also reduced considerably with increased concentrations of the chemical. However, the incorporation of /sup 14/C-radio-activity in the extracellular slime generally enhanced due to the treatment, upto 6 hr after injection of the radioactivity, which declined significantly later at 15 hr, indicating a qualitative difference in the extracellular polysaccharides produced by the insecticide treated cells. The insecticide treatment drastically reduced the incorporation of /sup 32/P-disodium hydrogen phosphate into Rhizobium cells, but enhanced the specific activity of the extracellular polysacchrides.

  20. Isotopic signatures (13C/12C; 15N/14N) of blue penguin burrow soil invertebrates : carbon sources and trophic relationships

    International Nuclear Information System (INIS)

    Hawke, D.J.; Clark, J.M.

    2010-01-01

    Seabird burrows provide a soil environment for processing discards such as feathers and guano, hence constituting a primary interface between the sea and the land. This study involved collection and culturing of soil invertebrates from three blue penguin (Eudyptula minor) burrows, and examined their 13 C/ 12 C and 15 N/ 14 N isotopic composition in relation to potential burrow resources (terrestrial plant litter, burrow soil, guano, blue penguin feathers). Two taxa (cerylonid beetles and small tineid moth larvae) had a depleted 13 C/ 12 C indicative of a level of dependence on C from terrestrial soil. Tineid moth larvae (Monopis crocicapitella and (or) M. ethelella) substantially increased their 13 C/ 12 C enrichment during development, implying increasing dependence on marine C. Remaining taxa, both decomposers and predators, had 13 C/ 12 C intermediate between guano and feathers. Larval and emergent fleas had the most enriched 13 C/ 12 C , indicative of a greater dependence on feather C and the likelihood of co-processing with guano. Pseudoscorpions and histerid beetles had overlapping isotopic enrichments implying competition for prey, but were spatially separated in burrow soil. With their highly enriched 15 N/ 14 N and marine 13 C/ 12 C, larvae and protonymphs of the histiostomatid mite Myianoetus antipodus stood alone. Blue penguin burrows therefore support a diverse invertebrate fauna that incorporates terrestrial soil as well as varying proportions of the various blue penguin discards. (author). 45 refs., 1 fig., 1 tab.

  1. Effect of aldicarb on growth and radio-carbon (14C) and radio-phosphorus (32P) assimilation by Rhizobium japonicum

    International Nuclear Information System (INIS)

    Balasubramanian, A.; Nilakantan, Gita

    1976-01-01

    In vitro studies on the effect of aldicarb (2-methyl-2-(methyl thio) propionaldehde-o-methyl carbamoyl oxime), a soil applied systemic insecticide, on Rhizobium japonicum revealed that the chemical (at 1,2 and 5 ppm levels) stimulated the growth of the organism initially upto 48 hr which declined thereafter upto 72 hr. The incorporation of 14 C-glucose by the cells considerably reduced due to the insecticide treatment. The production of extracellular, water-soluble slime (polysacchardes) was also reduced considerably with increased concentrations of the chemical. However, the incorporation of 14 C-radio-activity in the extracellular slime generally enhanced due to the treatment, upto 6 hr after injection of the radioactivity, which declined significantly later at 15 hr, indicating a qualitative difference in the extracellular polysaccharides produced by the insecticide treated cells. The insecticide treatment drastically reduced the incorporation of 32 P-disodium hydrogen phosphate into Rhizobium cells, but enhanced the specific activity of the extracellular polysacchrides. (author)

  2. Tritium, carbon-14, and iodine-129 as indicators for localized vertical recharge along an anticline in the Columbia River Basalts using a decay-corrected mixing model

    Energy Technology Data Exchange (ETDEWEB)

    Hall, S.H.; Johnson, V.G.; Early, T.O.

    1987-11-01

    Tritium, /sup 14/C, and /sup 129/I in groundwater samples are used to demonstrate vertical recharge and measure flow velocity in the fractured and faulted Umtanum Ridge-Gable Mountain acticline, within the Columbia River Basalts, at a sampling site about 6 mi northeast of the proposed high-level nuclear waste repository at the Hanford Site, Washington State. Mixing model calculations yield an apparent downward migration rate of 15 to 19 ft/yr through a sequence of aquifers in the Wanapum Basalt that range in depth from 698 to 1373 ft. Estimates of the vertical flow rate in the overlying Saddle Mountains Basalt are somewhat higher. Hydrographs from neighboring wells, hydrostatic heads, pump test data, and the chemical composition of groundwater samples from the sampling well are consistent with interaquifer communication. Some hydrologic evidence from aquifers in this region suggests that, in the past, flow may have been upward. This possible reversal of flow may be associated with water table mounding in the unconfined aquifer, caused by waste disposal activities at the Hanford Site since World War II. 17 refs., 12 figs., 3 tabs.

  3. Tritium, carbon-14, and iodine-129 as indicators for localized vertical recharge along an anticline in the Columbia River Basalts using a decay-corrected mixing model

    International Nuclear Information System (INIS)

    Hall, S.H.; Johnson, V.G.; Early, T.O.

    1987-11-01

    Tritium, 14 C, and 129 I in groundwater samples are used to demonstrate vertical recharge and measure flow velocity in the fractured and faulted Umtanum Ridge-Gable Mountain acticline, within the Columbia River Basalts, at a sampling site about 6 mi northeast of the proposed high-level nuclear waste repository at the Hanford Site, Washington State. Mixing model calculations yield an apparent downward migration rate of 15 to 19 ft/yr through a sequence of aquifers in the Wanapum Basalt that range in depth from 698 to 1373 ft. Estimates of the vertical flow rate in the overlying Saddle Mountains Basalt are somewhat higher. Hydrographs from neighboring wells, hydrostatic heads, pump test data, and the chemical composition of groundwater samples from the sampling well are consistent with interaquifer communication. Some hydrologic evidence from aquifers in this region suggests that, in the past, flow may have been upward. This possible reversal of flow may be associated with water table mounding in the unconfined aquifer, caused by waste disposal activities at the Hanford Site since World War II. 17 refs., 12 figs., 3 tabs

  4. Enhanced low-level LSC performance for carbon-14 dating using a bismuth germanate (Bi4Ge3O12) quasi-active guard

    International Nuclear Information System (INIS)

    Cook, G.T.

    1995-01-01

    The Packard 2770TR/SL is a novel low-level liquid scintillation spectrometer which employs bismuth germanate (BGO - Bi 4 Ge 3 O 12 ) as a quasi-active guard to reduce background count rates and improve limits of detection. The results of this study indicate that this system shows tremendous potential for radiocarbon dating. Its great advantage is that it can give exceptional performance using standard low 40 K borosilicate glass vials costing only a few cents each. For example, in an optimized counting window, 4.6-mL 14 C benzene contained in a standard 7-mL glass vial produced a background count rate of 0.49 cpm and an efficiency of 70.3%, yielding a figure of merit (E 2 V 2 /B) value of 213,000 ±9,000 (where B = background count rate in counts per minute [cpm], E = percentage efficiency, and V = volume of benzene). This performance is comparable to published data for low-level instruments which employ active coincidence guard detectors and standard glass vials. When the same vials were recounted in vial holders, specially fabricated from BGO, the corresponding optimum values for background, efficiency and figure of merit, respectively, were 0.24 cpm, 61.0% and 328,000 ± 19,000. This performance is comparable to that of other low-level counting instruments when they are used in combination with specialized Teflon and silica vials. The BGO vial holders were also used in previous generations of Packard instruments which employ time resolved liquid scintillation counting (TR-LSC) for electronic background reduction and this resulted in significant improvements in performance

  5. Stable carbon (12/13C) and nitrogen (14/15N) isotopes as a tool for identifying the sources of cyanide in wastes and contaminated soils-A method development

    International Nuclear Information System (INIS)

    Weihmann, Jenny; Mansfeldt, Tim; Schulte, Ulrike

    2007-01-01

    The occurrence of iron-cyanide complexes in the environment is of concern, since they are potentially hazardous. In order to determine the source of iron-cyanide complexes in contaminated soils and wastes, we developed a method based on the stable isotope ratios 13 C/ 12 C and 15 N/ 14 N of the complexed cyanide-ion (CN - ). The method was tested on three pure chemicals and two industrials wastes: blast-furnace sludge (BFS) and gas-purifier waste (GPW). The iron-cyanide complexes were converted into the solid cupric ferrocyanide, Cu 2 [Fe(China) 6 ].7H 2 O, followed by combustion and determination of the isotope-ratios by continuous flow isotope ratio mass spectrometry. Cupric ferrocyanide was obtained from the materials by (i) an alkaline extraction with 1 M NaOH and (ii) a distillate digestion. The [Fe(China) 6 ] 4- of the alkaline extraction was precipitated after adding Cu 2+ . The CN - of the distillate digestion was at first complexed with Fe 2+ under inert conditions and then precipitated after adding Cu 2+ . The δ 13 C-values obtained by the two methods differed slightly up to 1-3 per mille for standards and BFS. The difference was larger for alkaline-extracted GPW (4-7 per mille ), since non-cyanide C was co-extracted and co-precipitated. Therefore the distillate digestion technique is recommended when determining the C isotope ratios in samples rich in organic carbon. Since the δ 13 C-values of BFS are in the range of -30 to -24 per mille and of -17 to -5 per mille for GPW, carbon seems to be a suitable tracer for identifying the source of cyanide in both wastes. However, the δ 15 N-values overlapped for BFS and GPW, making nitrogen unsuitable as a tracer

  6. The risk of leukaemia in young children from exposure to tritium and carbon-14 in the discharges of German nuclear power stations and in the fallout from atmospheric nuclear weapons testing

    Energy Technology Data Exchange (ETDEWEB)

    Wakeford, Richard [The University of Manchester, Centre for Occupational and Environmental Health, Institute of Population Health, Manchester (United Kingdom)

    2014-05-15

    Towards the end of 2007, the results were published from a case-control study (the ''KiKK Study'') of cancer in young children, diagnosed <5 years of age during 1980-2003 while resident near nuclear power stations in western Germany. The study found a tendency for cases of leukaemia to live closer to the nearest nuclear power station than their matched controls, producing an odds ratio that was raised to a statistically significant extent for residence within 5 km of a nuclear power station. The findings of the study received much publicity, but a detailed radiological risk assessment demonstrated that the radiation doses received by young children from discharges of radioactive material from the nuclear reactors were much lower than those received from natural background radiation and far too small to be responsible for the statistical association reported in the KiKK Study. This has led to speculation that conventional radiological risk assessments have grossly underestimated the risk of leukaemia in young children posed by exposure to man-made radionuclides, and particular attention has been drawn to the possible role of tritium and carbon-14 discharges in this supposedly severe underestimation of risk. Both {sup 3}H and {sup 14}C are generated naturally in the upper atmosphere, and substantial increases in these radionuclides in the environment occurred as a result of their production by atmospheric testing of nuclear weapons during the late 1950s and early 1960s. If the leukaemogenic effect of these radionuclides has been seriously underestimated to the degree necessary to explain the KiKK Study findings, then a pronounced increase in the worldwide incidence of leukaemia among young children should have followed the notably elevated exposure to {sup 3}H and {sup 14}C from nuclear weapons testing fallout. To investigate this hypothesis, the time series of incidence rates of leukaemia among young children <5 years of age at diagnosis has been

  7. The risk of leukaemia in young children from exposure to tritium and carbon-14 in the discharges of German nuclear power stations and in the fallout from atmospheric nuclear weapons testing.

    Science.gov (United States)

    Wakeford, Richard

    2014-05-01

    Towards the end of 2007, the results were published from a case-control study (the "KiKK Study") of cancer in young children, diagnosed study found a tendency for cases of leukaemia to live closer to the nearest nuclear power station than their matched controls, producing an odds ratio that was raised to a statistically significant extent for residence within 5 km of a nuclear power station. The findings of the study received much publicity, but a detailed radiological risk assessment demonstrated that the radiation doses received by young children from discharges of radioactive material from the nuclear reactors were much lower than those received from natural background radiation and far too small to be responsible for the statistical association reported in the KiKK Study. This has led to speculation that conventional radiological risk assessments have grossly underestimated the risk of leukaemia in young children posed by exposure to man-made radionuclides, and particular attention has been drawn to the possible role of tritium and carbon-14 discharges in this supposedly severe underestimation of risk. Both (3)H and (14)C are generated naturally in the upper atmosphere, and substantial increases in these radionuclides in the environment occurred as a result of their production by atmospheric testing of nuclear weapons during the late 1950s and early 1960s. If the leukaemogenic effect of these radionuclides has been seriously underestimated to the degree necessary to explain the KiKK Study findings, then a pronounced increase in the worldwide incidence of leukaemia among young children should have followed the notably elevated exposure to (3)H and (14)C from nuclear weapons testing fallout. To investigate this hypothesis, the time series of incidence rates of leukaemia among young children risk of leukaemia in young children following the peak of above-ground nuclear weapons testing, or that incidence rates are related to level of exposure to fallout, is

  8. Soil, climate and the environment - an indissociable threesome. Soil carbon and global changes: reciprocal impacts; Carbon in all its forms; Echomicadas, a new tool to analyse carbon 14; Biotransformation of metallic trace elements by soil micro-organisms; Absorption and distribution of metallic elements in plants; Dynamics of metallic contaminants in agricultural systems; Is photo-remediation for tomorrow? Hyper-accumulator plants; Sediments, tell me the Seine history... The complex history of plant feeding by the soil; The environmental analysis

    International Nuclear Information System (INIS)

    Hatte, Christine; Tisnerat-Laborde, Nadine; Ayrault, Sophie; Balesdent, Jerome; Chapon, Virginie; Bourguignon, Jacques; Alban, Claude; Ravanel, Stephane; Denaix, Laurence; Nguyen, Christophe; Vavasseur, Alain; Sarrobert, Catherine; Gasperi, Johnny; Latrille, Christelle; Savoye, Sebastien; Augusto, Laurent; Conan Labbe, Annie; Bernard Michel, Bruno; Douysset, Guilhem; Toqnelli, Antoine; Vailhen, Dominique; Moulin, Christophe

    2016-01-01

    The articles of this file on the relationships between soils, climate and the environment discuss the reciprocal impacts of soil carbon and global changes with the objective of reduction of greenhouse effect and of increase of carbon sequestration; the various forms of carbon are presented and their properties commented ; a compact radiocarbon system (ECHoMiCADAS) is presented, developed by the Laboratory of sciences of climate and environment (LSCE) and designed for the analysis of carbon 14; an article describes how micro-organisms can play a crucial role in the transformation of soil pollutants by modifying their chemical speciation and thus their toxicity; strategies based on the absorption of metallic trace elements present in the soil to control physiological processes in plants are discussed, with applications to agriculture, food supply and to the environment; researches related to the study of effects of metallic contaminants in agricultural systems are evoked, and the reasons for a slow development of phyto-technologies, notably phyto-remediation, for pollution control and decontamination of soils and liquid media, are explained. Other themes are presented : hyper-accumulator plants which present very high contents of non-essential (As, Cd, Hg, Pb, Se) or essential (Co, Cu, Fe, Mn, Mo, Ni) elements, are slowly growing, and display a limited biomass, but could be used for a phyto-extraction of metals from contaminated soils; how analysis and dating of sediments can reveal the presence of contaminants, and therefore give an insight into human activities and regulations, and into their impact on the river; how plants are able to develop strategies in their search for nutrients in different types of soils, even poor ones, and presentation of the various disciplines, methods and techniques used for environmental analysis with their applications to installation and site control, or to the study of pollutant migration

  9. Microprobe analysis of carbon gradients

    International Nuclear Information System (INIS)

    Lamothe, M.; Convert, F.

    1987-01-01

    Problems arising in carbon analysis and how they are solved are presented: sample pollution limitation using cold trap and gas jet cleaning sample preparation, carbon content determination and calibration, automation and optimization. Examples given include concentration monitoring. Carbon homogeneity after complete cementation and decarburization by heat treatment. 6 refs, 14 figs [fr

  10. SATS 14

    DEFF Research Database (Denmark)

    Frølunde, Lisbeth; Andreasen, Lars Birch; Hansen, Susanne Pihl

    SATS14 projektet har drejet sig om at undersøge mulighederne i at kunne tilbyde en særlig indsats til de produktionsskoleelever, der har brug for det, så vidt muligt lokalt på deres skole. Projektets formål har været at indhente erfaringer med at tilbyde elever på 14 produktionsskoler på Sjælland...... mål. SATS14 kan dermed ses i en større social sammenhæng. Der er en stigende erkendelse af behovet for initiativer til at hjælpe de elever, der oplever psykiske vanskeligheder. I forordet til en rapport fra Undervisningsministeriet om erhvervsuddannelser beskrives målet: ”95 procent af en...... ungdomsårgang i 2015 skal gennemføre en ungdomsuddannelse… For at opfylde regeringens mål… er det nødvendigt med en særlig indsats for at fastholde de unge, som begynder i en uddannelse, herunder også de bogligt svage” (Kirkegaard og Nielsen, 2008). Da SATS14 projektet startede, var der ikke megen opmærksomhed...

  11. Stable carbon ({sup 12/13}C) and nitrogen ({sup 14/15}N) isotopes as a tool for identifying the sources of cyanide in wastes and contaminated soils-A method development

    Energy Technology Data Exchange (ETDEWEB)

    Weihmann, Jenny [Arbeitsgruppe Bodengeographie/Bodenkunde, Geographisches Institut, Universitaet zu Koeln, D-50923 Cologne (Germany); Mansfeldt, Tim [Arbeitsgruppe Bodengeographie/Bodenkunde, Geographisches Institut, Universitaet zu Koeln, D-50923 Cologne (Germany)]. E-mail: tim.mansfeldt@uni-koeln.de; Schulte, Ulrike [Lehrstuhl fuer Sediment- und Isotopengeologie, Institut fuer Geologie, Mineralogie und Geophysik, Ruhr-Universitaet Bochum, D-44780 Bochum (Germany)

    2007-01-23

    The occurrence of iron-cyanide complexes in the environment is of concern, since they are potentially hazardous. In order to determine the source of iron-cyanide complexes in contaminated soils and wastes, we developed a method based on the stable isotope ratios {sup 13}C/{sup 12}C and {sup 15}N/{sup 14}N of the complexed cyanide-ion (CN{sup -}). The method was tested on three pure chemicals and two industrials wastes: blast-furnace sludge (BFS) and gas-purifier waste (GPW). The iron-cyanide complexes were converted into the solid cupric ferrocyanide, Cu{sub 2}[Fe(China){sub 6}].7H{sub 2}O, followed by combustion and determination of the isotope-ratios by continuous flow isotope ratio mass spectrometry. Cupric ferrocyanide was obtained from the materials by (i) an alkaline extraction with 1 M NaOH and (ii) a distillate digestion. The [Fe(China){sub 6}]{sup 4-} of the alkaline extraction was precipitated after adding Cu{sup 2+}. The CN{sup -} of the distillate digestion was at first complexed with Fe{sup 2+} under inert conditions and then precipitated after adding Cu{sup 2+}. The {delta} {sup 13}C-values obtained by the two methods differed slightly up to 1-3 per mille for standards and BFS. The difference was larger for alkaline-extracted GPW (4-7 per mille ), since non-cyanide C was co-extracted and co-precipitated. Therefore the distillate digestion technique is recommended when determining the C isotope ratios in samples rich in organic carbon. Since the {delta} {sup 13}C-values of BFS are in the range of -30 to -24 per mille and of -17 to -5 per mille for GPW, carbon seems to be a suitable tracer for identifying the source of cyanide in both wastes. However, the {delta} {sup 15}N-values overlapped for BFS and GPW, making nitrogen unsuitable as a tracer.

  12. The use of 14C ethanolamine as a precursor

    International Nuclear Information System (INIS)

    Madelmont, J.C.; Parry, D.; Godeneche, D.; Duprat, J.

    1985-01-01

    Two new 2 chloroethyl nitrosoureas were labelled on two positions by 14 C starting from Na 14 CN and using 14 C ethanolamine as intermediate, i.e. on the carbon 2 of the 2 chloro ethyl group and on the carbon 2 of the cysteamine part. (author)

  13. Synthesis of [3-14C]- and [phenyl-U-14C] olaquindox

    International Nuclear Information System (INIS)

    Maul, W.; Scherling, D.; Seng, F.

    1981-01-01

    Olaquindox is a new feed additive. [ 14 C]Olaquindox, labelled in different positions, was needed for tracer-studies of pharmacokinetics, biotransformation and residues in several species of animals. 2-[N-(2-hydroxethyl)-carbamoyl]-3-methyl-[3- 14 C]quinoxaline-1,4-dioxide([3- 14 C]Olaquindox) was synthesized from barium[ 14 C]carbonate (22 mmoles; 1.15 Ci) via [1- 14 C]acetic acid, sodium[1- 14 C]acetate, [1- 14 C]acetylchloride, ethyl[3- 14 C]acetoacetate and 2-carbethoxy-3-methyl-[3- 14 C]quinoxaline-1,4-dioxide with an overall yield of 10%, based on barium[ 14 C]carbonate. The radiochemical purity was better than 98% (tlc). The specific activities of three preparations were 10.5, 8.4 and 5.45 μCi/mg respectively. [phenyl-U- 14 C]Olaquindox was synthesized starting from [U- 14 C]aniline (19.8 mmoles; 284.4 mCi). Intermediate products were N-acetyl[U- 14 C]aniline, 2-nitro-N-acetyl[U- 14 C]aniline, 2-nitro[U- 14 C]aniline and [U- 14 C]benzofurazanoxide. The total yield was 50% as calculated for [U- 14 C]aniline. At calibration samples of two preparations showed specific activities of 49.5 and 11.1 μCi/mg respectively. The radiochemical purity was checked by tlc and exceeded 98%. (author)

  14. ESDに向けての14C測定の利用

    OpenAIRE

    中村, 俊夫; 太田, 友子; 西田, 真砂美; Nakamura, Toshio; Ohta, Tomoko; Nishida, Masami

    2015-01-01

    We have measured 14C concentration of plastic bag samples to confirm that the plastic bags were produced from sustainable carbon, carbon contained in living plants, instead of fossil carbon. Three plastic bags used for normal shopping of food carrier had descriptions on the bag that they were produced from sustainable carbon in some amount. To check the amount of carbon from recent plant remains, we have measured 14C concentrations of the plastic bag samples. The 14C contents were consistent ...

  15. 14C measurements in aquifers with methane

    International Nuclear Information System (INIS)

    Barker, J.F.; Fritz, P.; Brown, R.M.

    1978-01-01

    A survey of various groundwater systems indicates that methane is a common trace constituent and occasionally a major carbon species in groundwaters. Thermocatalytic methane had delta 13 CCH 4 > -45% 0 and microbially-produced or biogenic methane had delta 13 CCH 4 0 . Groundwaters containing significant biogenic methane had abnormally heavy delta 13 C values for the inorganic carbon. Thermocatalytic methane had no apparent effect on the inorganic carbon. Because methanogenesis seriously affects the carbon isotope geochemistry of groundwaters, the correction of raw 14 C ages of affected groundwaters must consider these effects. Conceptual models are developed which adjust the 14 C activity of the groundwater for the effects of methanogenesis and for the dilution of carbon present during infiltration by simple dissolution of rock carbonate. These preliminary models are applied to groundwaters from the Alliston sand aquifer where methanogenesis has affected most samples. In this system, methanogenic bacteria using organic matter present in the aquifer matrix as substrate, have added inorganic carbon to the groundwater which has initiated further carbonate rock dissolution. These processes have diluted the inorganic carbon 14 C activity. (orig.) [de

  16. Decomposition performance of animals as an indicator of stress acting on beech-forest ecosystems - microcosmos experiments with carbon-14-labelled litter components. Final report. Die Zersetzungsleistung der Tiere als Indikator fuer die Belastung von Buchenwald-Oekosystemen - Mikrokosmosexperimente mit sup 14 C markierten Streukomponenten. Abschlussbericht

    Energy Technology Data Exchange (ETDEWEB)

    Schaefer, M.; Wolters, V.

    1988-01-01

    The effect of acid rain and heavy metals on the biotic interactions in the soil of beech forest with mull, must, and limed must was investigated with the aid of close-to-nature microcosmos systems. Parameters made use of were the decomposition of carbon-14-labelled litter components and the turnover of the microflora in C, N, and P. As the results show, increased proton uptake will bear on rearly every stage of the decomposition process in mull soils. As a result, there may be litter accumulation on the ground and first signs of humus disintegration in the mineral soil of mull soils. A direct relation between the acidity of the environment and the extent of decomposition inhibition does not exist. Despite wide-ranging impairment of edaphic animals, the activity of the ground fauna still is to be considered as the most important buffer system of soils rich in bases. Acidic condition of the beech forest soils with the humus form 'must' led to drastic inhibition of litter decomposition, to a change of the effect of edaphic animals, and to an increase in N mineralization. The grazing animals frequently aggravate the decomposition inhibition resulting from acid precipitation. The comparision of the decomposition process in a soil containing must as compared to one containing mull showed acidic soils to be on a lower biological buffer level than soils rich in bases. The main buffer capacity of acidic soils lies in the microflora, which is adapted to sudden increases in acidity and which recovers quickly. In the opinion of the authors, simple liming is not enough to increase the long-term biogenic stability of a forest ecosystem. A stabilizing effect of the fauna, for instance on nitrogen storage, is possible only if forest care measuries are carried out, for instance careful loosening of the mineral soil, which will attract earthworm species penetrating deeply into the soil. (orig./MG) With 12 refs., 6 figs.

  17. Occult Carbon Monoxide Poisoning

    OpenAIRE

    Kirkpatrick, John N.

    1987-01-01

    A syndrome of headache, fatigue, dizziness, paresthesias, chest pain, palpitations and visual disturbances was associated with chronic occult carbon monoxide exposure in 26 patients in a primary care setting. A causal association was supported by finding a source of carbon monoxide in a patient's home, workplace or vehicle; results of screening tests that ruled out other illnesses; an abnormally high carboxyhemoglobin level in 11 of 14 patients tested, and abatement or resolution of symptoms ...

  18. Carbon used in electrotechnology

    International Nuclear Information System (INIS)

    Coulon, M.; Reynvaan, C.; Maire, J.

    1994-01-01

    The carbon is the essential or single component of several materials. After having recalled the general properties of carbon and graphite some traditional processes of fabrication are described and some new products are studied then we tackle the applications with electric current: -electrodes in the electric piles where we use the carbon chemical inertia -coals of electric arc where we use the refractory properties and the low resistivity of graphite -Joule effect where we work on an enough wide field of material resistivity -electric fixed or sliding contacts where in addition to the refractory properties it is its unweldability which makes it indispensable particularly in the brooms for electric motors. The future is good for carbon and its compounds particularly for the new discovered fullerenes, spheric molecules of carbon, the properties of which are bad known (supraconductivity, lubrication, energy storage). 21 refs., 26 figs., 14 tab

  19. Synthesis of carbon-14 labelled cis-malonato [(4R,5R)-4,5-bis(aminomethyl)-2-isopropyl-1,3-dioxolane] platinum(II) (SKI 2053R)

    International Nuclear Information System (INIS)

    Kim, Dae-Kee; Kim, Youngseok; Rim, Jonggill; Kim, Ganghyeok; Gam, Jongsik; Song, Sungkun; Yoo, Kwanghee; Kim, Key H.

    1994-01-01

    The synthesis of 14 C-labelled cis-malonato[(4R,5R)-4,5-bis(aminomethyl)-2-isopropyl-1,3-dioxolan e]platinum(II) from [1,4- 14 C] D-tartaric acid is described. The overall radiochemical yield of the product in a eight-step sequence was 23.8% and radiochemical purity was 98.5%. (author)

  20. Measurements of 14C in ancient ice from Taylor Glacier, Antarctica constrain in situ cosmogenic 14CH4 and 14CO production rates

    Science.gov (United States)

    Petrenko, Vasilii V.; Severinghaus, Jeffrey P.; Schaefer, Hinrich; Smith, Andrew M.; Kuhl, Tanner; Baggenstos, Daniel; Hua, Quan; Brook, Edward J.; Rose, Paul; Kulin, Robb; Bauska, Thomas; Harth, Christina; Buizert, Christo; Orsi, Anais; Emanuele, Guy; Lee, James E.; Brailsford, Gordon; Keeling, Ralph; Weiss, Ray F.

    2016-03-01

    Carbon-14 (14C) is incorporated into glacial ice by trapping of atmospheric gases as well as direct near-surface in situ cosmogenic production. 14C of trapped methane (14CH4) is a powerful tracer for past CH4 emissions from ;old; carbon sources such as permafrost and marine CH4 clathrates. 14C in trapped carbon dioxide (14CO2) can be used for absolute dating of ice cores. In situ produced cosmogenic 14C in carbon monoxide (14CO) can potentially be used to reconstruct the past cosmic ray flux and past solar activity. Unfortunately, the trapped atmospheric and in situ cosmogenic components of 14C in glacial ice are difficult to disentangle and a thorough understanding of the in situ cosmogenic component is needed in order to extract useful information from ice core 14C. We analyzed very large (≈1000 kg) ice samples in the 2.26-19.53 m depth range from the ablation zone of Taylor Glacier, Antarctica, to study in situ cosmogenic production of 14CH4 and 14CO. All sampled ice is >50 ka in age, allowing for the assumption that most of the measured 14C originates from recent in situ cosmogenic production as ancient ice is brought to the surface via ablation. Our results place the first constraints on cosmogenic 14CH4 production rates and improve on prior estimates of 14CO production rates in ice. We find a constant 14CH4/14CO production ratio (0.0076 ± 0.0003) for samples deeper than 3 m, which allows the use of 14CO for correcting the 14CH4 signals for the in situ cosmogenic component. Our results also provide the first unambiguous confirmation of 14C production by fast muons in a natural setting (ice or rock) and suggest that the 14C production rates in ice commonly used in the literature may be too high.

  1. Syntheses of [6-14C] and [5-carboxy, 6-14C2]nitrendipine

    International Nuclear Information System (INIS)

    Maul, N.; Scherling, D.

    1989-01-01

    [6- 14 C]Nitrendipine synthesis started from barium[ 14 ]carbonate, which was converted to [1- 14 C]acetyl chloride. The acid chloride was condensed with Meldrum's acid (2,2-dimethyl-1,3-dioxane-4,6-dione). The resulting intermediate was treated with boiling methanol to give methyl [3- 14 C]acetoacetate. The reaction with gaseous ammonia in toluene yielded the corresponding methyl 3-amino[3- 14 C]crotonate which was condensed with ethyl 2-(3-nitro-benzylidene) acetoacetate to obtain [6- 14 C]nitrendipine. (author)

  2. Syntheses of (6- sup 14 C) and (5-carboxy, 6- sup 14 C sub 2 )nitrendipine

    Energy Technology Data Exchange (ETDEWEB)

    Maul, N.; Scherling, D. (Bayer AG, Wuppertal (Germany, F.R.). Inst. fuer Pharmakologie)

    1989-04-01

    (6-{sup 14}C)Nitrendipine synthesis started from barium({sup 14})carbonate, which was converted to (1-{sup 14}C)acetyl chloride. The acid chloride was condensed with Meldrum's acid (2,2-dimethyl-1,3-dioxane-4,6-dione). The resulting intermediate was treated with boiling methanol to give methyl (3-{sup 14}C)acetoacetate. The reaction with gaseous ammonia in toluene yielded the corresponding methyl 3-amino(3-{sup 14}C)crotonate which was condensed with ethyl 2-(3-nitro-benzylidene) acetoacetate to obtain (6-{sup 14}C)nitrendipine. (author).

  3. Occult carbon monoxide poisoning.

    Science.gov (United States)

    Kirkpatrick, J N

    1987-01-01

    A syndrome of headache, fatigue, dizziness, paresthesias, chest pain, palpitations and visual disturbances was associated with chronic occult carbon monoxide exposure in 26 patients in a primary care setting. A causal association was supported by finding a source of carbon monoxide in a patient's home, workplace or vehicle; results of screening tests that ruled out other illnesses; an abnormally high carboxyhemoglobin level in 11 of 14 patients tested, and abatement or resolution of symptoms when the source of carbon monoxide was removed. Exposed household pets provided an important clue to the diagnosis in some cases. Recurrent occult carbon monoxide poisoning may be a frequently overlooked cause of persistent or recurrent headache, fatigue, dizziness, paresthesias, abdominal pain, diarrhea and unusual spells.

  4. Transformation of the herbicide [14C]glufosinate in soils

    International Nuclear Information System (INIS)

    Smith, A.E.

    1989-01-01

    The degradation of 2 μg/g [ 14 C]glufosinate (DL-homoalan-4-ylmethylphosphinic acid) was studied in clay, clay loam, and sandy loam soils at 85% field capacity and at 20 degree C. Over a 4-week period the soils were extracted and analyzed for transformation products by radiochemical and gas chromatographic techniques. In all soils there was release of [ 14 C]carbon dioxide and formation of [ 14 C]-3-(hydroxymethylphosphinyl)propionic acid (MPPA) as major degradation products. Within 21 days, about 55% of the applied 14 C herbicide had been transformed to MPPA in the sandy loam and 19% to [ 14 C]carbon dioxide. After 28 days, approximately 45% of the 14 C herbicide had been transformed to MPPA in the clay and clay loam and 10% released as [ 14 C]carbon dioxide. At all samplings, other 14 C transformation products appeared to be insignificant

  5. 14 CFR 14.25 - Settlement.

    Science.gov (United States)

    2010-01-01

    ... 14 Aeronautics and Space 1 2010-01-01 2010-01-01 false Settlement. 14.25 Section 14.25 Aeronautics... IMPLEMENTING THE EQUAL ACCESS TO JUSTICE ACT OF 1980 Procedures for Considering Applications § 14.25 Settlement. The applicant and agency counsel may agree on a proposed settlement of the award before final action...

  6. 14 CFR 380.14 - Unused space.

    Science.gov (United States)

    2010-01-01

    ... 14 Aeronautics and Space 4 2010-01-01 2010-01-01 false Unused space. 380.14 Section 380.14 Aeronautics and Space OFFICE OF THE SECRETARY, DEPARTMENT OF TRANSPORTATION (AVIATION PROCEEDINGS) SPECIAL REGULATIONS PUBLIC CHARTERS Conditions and Limitations § 380.14 Unused space. Noting contained in this part...

  7. Conducting carbonized polyaniline nanotubes

    International Nuclear Information System (INIS)

    Mentus, Slavko; Ciric-Marjanovic, Gordana; Trchova, Miroslava; Stejskal, Jaroslav

    2009-01-01

    Conducting nitrogen-containing carbon nanotubes were synthesized by the carbonization of self-assembled polyaniline nanotubes protonated with sulfuric acid. Carbonization was carried out in a nitrogen atmosphere at a heating rate of 10 deg. C min -1 up to a maximum temperature of 800 deg. C. The carbonized polyaniline nanotubes which have a typical outer diameter of 100-260 nm, with an inner diameter of 20-170 nm and a length extending from 0.5 to 0.8 μm, accompanied with very thin nanotubes with outer diameters of 8-14 nm, inner diameters 3.0-4.5 nm and length extending from 0.3 to 1.0 μm, were observed by scanning and transmission electron microscopies. Elemental analysis showed 9 wt% of nitrogen in the carbonized product. Conductivity of the nanotubular PANI precursor, amounting to 0.04 S cm -1 , increased to 0.7 S cm -1 upon carbonization. Molecular structure of carbonized polyaniline nanotubes has been analyzed by FTIR and Raman spectroscopies, and their paramagnetic characteristics were compared with the starting PANI nanotubes by EPR spectroscopy.

  8. Conducting carbonized polyaniline nanotubes

    Energy Technology Data Exchange (ETDEWEB)

    Mentus, Slavko; Ciric-Marjanovic, Gordana [Faculty of Physical Chemistry, University of Belgrade, Studentski trg 12-16, 11158 Belgrade (Serbia); Trchova, Miroslava; Stejskal, Jaroslav [Institute of Macromolecular Chemistry, Academy of Sciences of the Czech Republic, Heyrovsky Square 2, 162 06 Prague 6 (Czech Republic)], E-mail: gordana@ffh.bg.ac.rs

    2009-06-17

    Conducting nitrogen-containing carbon nanotubes were synthesized by the carbonization of self-assembled polyaniline nanotubes protonated with sulfuric acid. Carbonization was carried out in a nitrogen atmosphere at a heating rate of 10 deg. C min{sup -1} up to a maximum temperature of 800 deg. C. The carbonized polyaniline nanotubes which have a typical outer diameter of 100-260 nm, with an inner diameter of 20-170 nm and a length extending from 0.5 to 0.8 {mu}m, accompanied with very thin nanotubes with outer diameters of 8-14 nm, inner diameters 3.0-4.5 nm and length extending from 0.3 to 1.0 {mu}m, were observed by scanning and transmission electron microscopies. Elemental analysis showed 9 wt% of nitrogen in the carbonized product. Conductivity of the nanotubular PANI precursor, amounting to 0.04 S cm{sup -1}, increased to 0.7 S cm{sup -1} upon carbonization. Molecular structure of carbonized polyaniline nanotubes has been analyzed by FTIR and Raman spectroscopies, and their paramagnetic characteristics were compared with the starting PANI nanotubes by EPR spectroscopy.

  9. Influence of organic carbon sources and isotope exchange processes between water and nitrate on the fractionation of the stable isotopes 15N/14N and 18O/16O in dissolved nitrate during microbial dentrification in groundwater

    International Nuclear Information System (INIS)

    Wunderlich, Anja A.L.

    2012-01-01

    Stable isotopes of nitrate are commonly used to determine sources and degradation of nitrate. In this study, nitrite oxidizing bacteria were found to promote an oxygen isotope exchange between water and nitrate under anoxic conditions. Also, different carbon sources were found to influence the enrichment of stable isotopes in nitrate during microbial denitrification. Both results refine the stable isotope model of nitrate in respect to nitrate source determination and microbial nitrate reduction.

  10. Partial pressure (or fugacity) of carbon dioxide, temperature, salinity and other variables collected from the coastal surface underway observations using carbon dioxide gas analyzer, shower head equilibrator and other instruments from NOAA Ship Henry B. Bigelow in the North Atlantic Ocean, US North East coast from 2013-03-14 to 2013-11-19 (NCEI Accession 0162209)

    Data.gov (United States)

    National Oceanic and Atmospheric Administration, Department of Commerce — In February 2011, the Ocean Carbon Group at NOAA's Atlantic Oceanographic and Meteorological Laboratory (AOML) installed an instrument to measure CO2 levels in...

  11. Carbon/carbon composite materials

    International Nuclear Information System (INIS)

    Thebault, J.; Orly, P.

    2006-01-01

    Carbon/carbon composites are singular materials from their components, their manufacturing process as well as their characteristics. This paper gives a global overview of these particularities and applications which make them now daily used composites. (authors)

  12. 14C uncovers the past

    International Nuclear Information System (INIS)

    Anon.

    1977-01-01

    Radio-carbon dating, a method of dating prehistoric remains that has been developed since the Second World War, is based on the fact that all organic matter contains a radioactive isotope of carbon - 14 C- which, because it decays at a fixed rate, gives a good indication of the age of the substance. The CSIR's National Physical Research Laboratory entered the field of radio-carbon dating in 1967, when the Nature Isotopes Division was established. The division has become a world centre of excellence and much has been done to clear up the chronology of southern African prehistory. It has been found, for instance, that anatomically modern man appeared in southern Africa some 40000 years earlier than in Europe, and that the Zimbabwe ruins were built mainly around the year 1350 AD. The radio-carbon method can also be used to determine the age and flow rate of underground water and the rate at which tracer gases dissolve in the oceans, i.e. the efficiency with which the oceans cleanse the atmosphere from pollutants

  13. Synthesis of tritium and carbon-14 labelled N-(3-dimethyl aminopropyl)-N-(ethylaminocarbonyl)-6-(2-propenyl) ergoline-8β-carboxamide (cabergoline), a potent long lasting prolactin lowering agent

    International Nuclear Information System (INIS)

    Mantegani, S.; Brambilla, E.; Ermoli, A.; Fontana, E.; Angiuli, P.; Vicario, G.P.

    1991-01-01

    The syntheses of 3 H- and 14 C-labelled cabergoline and its analogues are described. Tritiated cabergoline ([ 3 H]cabergoline), namely N-(3-di-methylaminopropyl)-N-(ethylaminocarbonyl)-6-(2-[2,3- 3 H]-propenyl)ergoline-8β-carboxamide, was obtained, by catalytic reduction with tritium gas, according to two different synthetic procedures: A- a three step route, starting from 6-(2-propargyl)-dihydro lysergic acid-methyl ester gave [ 3 H]cabergoline, B - a one step route, starting from 1-ethyl-3-(3-dimethyl-aminopropyl)-3-[6'-(2-propargyl)ergoline-8'-carbonyl ]-urea 5' yielded [ 3 H]cabergoline. A modification of this last procedure also gave [ 3 H]dihydro cabergoline. The synthesis of [ 14 C]cabergoline was carried out, in a three step route, by addition of potassium [ 14 C]cyanide to 6-(2-propenyl)-8-chloroergoline to give the expected N-(dimethylaminopropyl)-N-(ethylaminocarbonyl)-6-(2-propenyl)-ergoline-8-[ 14 C]carboxamide, 97% radiochemically pure with a specific radioactivity of 2.09 GBq/mmol and an overall radiochemical yield of 16%. (author)

  14. Synthesis of tritium and carbon-14 labelled N-(3-dimethyl aminopropyl)-N-(ethylaminocarbonyl)-6-(2-propenyl) ergoline-8. beta. -carboxamide (cabergoline), a potent long lasting prolactin lowering agent

    Energy Technology Data Exchange (ETDEWEB)

    Mantegani, S.; Brambilla, E.; Ermoli, A.; Fontana, E.; Angiuli, P.; Vicario, G.P. (Farmitalia Carlo Erba s.r.l., Milan (Italy))

    1991-05-01

    The syntheses of {sup 3}H- and {sup 14}C-labelled cabergoline and its analogues are described. Tritiated cabergoline (({sup 3}H)cabergoline), namely N-(3-di-methylaminopropyl)-N-(ethylaminocarbonyl)-6-(2-(2,3-{sup 3}H)-propenyl)ergoline-8{beta}-carboxamide, was obtained, by catalytic reduction with tritium gas, according to two different synthetic procedures: A- a three step route, starting from 6-(2-propargyl)-dihydro lysergic acid-methyl ester gave ({sup 3}H)cabergoline, B - a one step route, starting from 1-ethyl-3-(3-dimethyl-aminopropyl)-3-(6'-(2-propargyl)ergoline-8'-carbonyl )-urea 5' yielded ({sup 3}H)cabergoline. A modification of this last procedure also gave ({sup 3}H)dihydro cabergoline. The synthesis of ({sup 14}C)cabergoline was carried out, in a three step route, by addition of potassium ({sup 14}C)cyanide to 6-(2-propenyl)-8-chloroergoline to give the expected N-(dimethylaminopropyl)-N-(ethylaminocarbonyl)-6-(2-propenyl)-ergoline-8-({sup 14}C)carboxamide, 97% radiochemically pure with a specific radioactivity of 2.09 GBq/mmol and an overall radiochemical yield of 16%. (author).

  15. 名古屋市におけるエアロゾル粒子中の14C濃度 : 炭素成分の発生源推定

    OpenAIRE

    本庄, 浩司; 中村, 俊夫; HONJYO, Koji; NAKAMURA, Toshio

    2011-01-01

    To estimate of the source of the carbon components, 14C concentration and carbon component measurements are performed for the aerosol particles collected in Nagoya city over a year. The high 14C concentration was seen on April and May. The average of 14C concentration suggests that half of the carbon components came from biomass carbon (BC). In addition, there were strong correlations between BC and Organic carbon (OC), fossil carbon (FC) and Elemental carbon (EC) concentrations. It is sugges...

  16. Use of carbon isotopes in studies of environmental contamination

    International Nuclear Information System (INIS)

    Aravena, R.; Olave, S.; Ortiz, J.

    1986-01-01

    This report informs the preliminary results of a study on tree leaves undertaken in various areas of Santiago, aired at evaluating the pollution levels reached by combustion of fossil fuels, using carbon - 14 and carbon - 13 as natural tracers. (Author)

  17. Radio carbonic dates (14C) from Dolores Fm. (Santa Lucia River,Canelones Department and Gutierrez chico Creek,Rio Negro Department)and comments about the vertebrate fauna associated

    International Nuclear Information System (INIS)

    Ubilla, M.

    1999-01-01

    Radiometric dates(14C)were performed based on fossil woods coming from late Pleistocene levels and assigned to dolores Fm.(Rio Negro Department, Gutierrez Chico Creek: Canelones Department, Danta Lucia basin).The 14C ages date the fossiliferous levels near the Pleistocene-Holocene boundary: 10.480+/-100 y B.P.(LP-1110,wood in det.), 10.500+/-110 y B.P. (LP-1143.wood in det.)and 11.650+/130 y B.P.(LP-509, Prosopis?sp.).Several ta xa of mammals recorded in the Dolores Fm.characterise the late Pleistocene of South Am erica( L ujunian f auna).Accordingly with the 14 dates, the most recent record of mega fauna of Uruguay is here reported.Archaeological sites with mega fauna have been described from other localities of South America with similar radiometric dates.In spite of the current controversy about the regional finipleistocenic climatic oscillation,the scarcely fossiliferous evidences suggest arid to semiarid and cold climatic condition.These evidences must be improved to test accurately the regional climatic hypothesis

  18. Carbonate aquifers

    Science.gov (United States)

    Cunningham, Kevin J.; Sukop, Michael; Curran, H. Allen

    2012-01-01

    Only limited hydrogeological research has been conducted using ichnology in carbonate aquifer characterization. Regardless, important applications of ichnology to carbonate aquifer characterization include its use to distinguish and delineate depositional cycles, correlate mappable biogenically altered surfaces, identify zones of preferential groundwater flow and paleogroundwater flow, and better understand the origin of ichnofabric-related karst features. Three case studies, which include Pleistocene carbonate rocks of the Biscayne aquifer in southern Florida and Cretaceous carbonate strata of the Edwards–Trinity aquifer system in central Texas, demonstrate that (1) there can be a strong relation between ichnofabrics and groundwater flow in carbonate aquifers and (2) ichnology can offer a useful methodology for carbonate aquifer characterization. In these examples, zones of extremely permeable, ichnofabric-related macroporosity are mappable stratiform geobodies and as such can be represented in groundwater flow and transport simulations.

  19. Preparation of a Lipopolysaccharide from Escherichia coli 01lla, 01llb, k58: h21 bacterial wall, labeled with carbon-14; Preparacion de un lipopolisacarido de la pared baceteriana de escherichia coli 01lla, 01llb, K58: H21, marcado con carbono-14

    Energy Technology Data Exchange (ETDEWEB)

    Solano Aunon, M. L.; Pacheco Lopez, J.; Garcia Pineda, M. D.; Roca, M.; Bayon, A.

    1981-07-01

    A brief description of the morphological and chemical structure of Li po polysaccharides is given, as well as its occurrence in nature and its mechanisms of action. It is emphasized the usefulness for actual biochemical and biomedical research of the labeled Lipopolysaccharide. The method for the labelling, isolation and purification of 14''C-Lipopolysacchari de is described. (Author) 23 refs.

  20. Preparation of a Lipopolysaccharide from Escherichia coli 01lla, 01llb, k58: h21 bacterial wall, labeled with carbon-14; Preparacion de un lipopolisacarido de la pared baceteriana de escherichia coli 01lla, 01llb, K58: H21, marcado con carbono-14

    Energy Technology Data Exchange (ETDEWEB)

    Solano Aunon, M L; Pacheco Lopez, J; Garcia Pineda, M D; Roca, M; Bayon, A

    1981-07-01

    A brief description of the morphological and chemical structure of Li po polysaccharides is given, as well as its occurrence in nature and its mechanisms of action. It is emphasized the usefulness for actual biochemical and biomedical research of the labeled Lipopolysaccharide. The method for the labelling, isolation and purification of 14''C-Lipopolysacchari de is described. (Author) 23 refs.

  1. Synthesis of 11-14C-quetiapine, 11-14C-isoclotiapine and 10-(4-methylpiperazin-1-yl)pyrido[4,3-b][1,4]benzothiazepine[10-14C

    International Nuclear Information System (INIS)

    Naghi Saadatjoo; Mohsen Javaheri; Nuclear Science and Technology Research Institute, Tehran; Nader Saemian; Mohsen Amini

    2016-01-01

    Quetiapine is one of the most widely used antipsychotic drug which acts as an antagonist for multiple neurotransmitter receptor sites. 2-[2-(4-(Dibenzo[b,f][1,4]thiazepin-11-yl)piperazin-1-yl)ethoxy]ethanol (quetiapine) labeled with carbon-14 in 11-position has been synthesized as part of a 5-step sequence from anthranilic acid-[carboxy- 14 C]. We have presented a convenient synthetic pathway for labeling of quetiapine with carbon-14 by using one-pot procedures from a key thiazepin-11(10H)-one-[11- 14 C] by good radiochemical yield. And also isoclotiapine[11- 14 C], and 10-(4-methylpiperazin-1-yl)pyrido[4,3-b][1,4]benzothiazepine[10- 14 C], synthesized according to this route. (author)

  2. Synthesis of 14C-radiolabelled Tilmicosin

    International Nuclear Information System (INIS)

    Crouse, G.D.; Terando, N.H.

    1989-01-01

    Tilmicosin was radiolabelled with carbon-14 on the 3,5-dimethylpiperidinyl sidechain as a requirement for animal metabolism studies. A new radiosynthesis of 3,5-dimethyl-piperidine was developed for this purpose. Incorporation into the desmycosin nucleus was accomplished by a reductive amination reaction. (author)

  3. The management of carbon-14 and iodine-129 wastes - a site specific survey of current and future arisings, possible management options and potential impact with respect to the United Kingdom

    International Nuclear Information System (INIS)

    Briggs, A.

    1988-06-01

    Part 1 - A site-specific survey, by the Harwell Laboratory, of current and future gaseous, liquid and solid arisings of 14 C and 129 I at UK nuclear installations, is presented in the form of tables and maps. In the tables the arisings are characterised in terms of quantity, activity and accompanying radionuclides. Management options discussed are: dispersal in the environment; capture and retention of arisings from power stations, reprocessing plants, and industrial sites producing pharmaceuticals and research materials; direct disposal of unprocessed spent fuel elements in an underground repository. Comparative costings of the various options are given. Part 2 - The information in part 1 is used by the National Radiological Protection Board as the basis for an examination of the effects that various management options would have on the radiological impact of 14 C and 129 I on the public. Comparison is made between different types of discharge, and disposal as a solid waste to various kinds of repository, in terms of their health detriment costs. Emphasis is placed on illustrating the use of a decision analysis methodology for assessment of the different waste management strategies. (author)

  4. Carbon-On-Carbon Manufacturing

    Science.gov (United States)

    Mungas, Gregory S. (Inventor); Buchanan, Larry (Inventor); Banzon, Jr., Jose T. (Inventor)

    2017-01-01

    The presently disclosed technology relates to carbon-on-carbon (C/C) manufacturing techniques and the resulting C/C products. One aspect of the manufacturing techniques disclosed herein utilizes two distinct curing operations that occur at different times and/or using different temperatures. The resulting C/C products are substantially non-porous, even though the curing operation(s) substantially gasify a liquid carbon-entrained filler material that saturates a carbon fabric that makes up the C/C products.

  5. Porous carbons

    Indian Academy of Sciences (India)

    R. Narasimhan (Krishtel eMaging) 1461 1996 Oct 15 13:05:22

    Abstract. Carbon in dense as well as porous solid form is used in a variety of applications. Activated porous carbons are made through pyrolysis and activation of carbonaceous natural as well as synthetic precursors. Pyrolysed woods replicate the structure of original wood but as such possess very low surface areas and ...

  6. Carbon photonics

    Energy Technology Data Exchange (ETDEWEB)

    Konov, V I [A M Prokhorov General Physics Institute, Russian Academy of Sciences, Moscow (Russian Federation)

    2015-11-30

    The properties of new carbon materials (single-crystal and polycrystalline CVD diamond films and wafers, single-wall carbon nanotubes and graphene) and the prospects of their use as optical elements and devices are discussed. (optical elements of laser devices)

  7. Partial pressure (or fugacity) of carbon dioxide, dissolved inorganic carbon, temperature, salinity and other variables collected from discrete sample and profile observations using CTD, bottle and other instruments from the AKADEMIK IOFFE in the South Pacific Ocean from 1992-02-14 to 1992-04-06 (NODC Accession 0115013)

    Data.gov (United States)

    National Oceanic and Atmospheric Administration, Department of Commerce — NODC Accession 0115013 includes chemical, discrete sample, physical and profile data collected from AKADEMIK IOFFE in the South Pacific Ocean from 1992-02-14 to...

  8. C14 Assays and Autoradiographic Studies on the Rooster Comb

    Science.gov (United States)

    Balazs, Endre A.; Szirmai, John A.; Bergendahl, Gudrun

    1959-01-01

    The distribution of C14 was studied in various parts of the rooster comb following treatment with testosterone. The value of gas-phase assay of C14 in tissue has been demonstrated and the results compared with those of autoradiographic studies on the same tissue. The results of these experiments showed that androgen treatment significantly increases the rate of incorporation of C14 in various parts of the comb. The specific activity of carbon in the comb, cornea, and liver differed, depending on which precursor, viz. glucose-6-C14, glucose-1-C14, and glucuronolactone-U-C14, was administered. The highest values were obtained after the administration of glucose-6-C14; glucuronolactone-U-C14 gave the lowest specific activity. The specific activity of carbon in different parts of the comb showed considerable variation. Carbon assay of serial sections of the comb cut at various planes showed that the specific activity of carbon was highest in the mucoid layer. Both C14 assays and autoradiograms indicate that C14 is also present in other parts of the comb. As seen in autoradiography, the concentration of C14 was highest in the epithelium, in the blood vessel walls, and in the avascular collagenous tissue. These results, and indications from previous studies, suggest that the high specific activity of carbon in the mucoid layer is due mainly to the presence of C14-labelled hyaluronic acid. Autoradiograms and PAS staining suggest that a significant amount of C14 is also incorporated into the glycoproteins associated with the collagen fibers. PMID:13654453

  9. Degradation of multiwall carbon nanotubes by bacteria

    International Nuclear Information System (INIS)

    Zhang, Liwen; Petersen, Elijah J.; Habteselassie, Mussie Y.; Mao, Liang; Huang, Qingguo

    2013-01-01

    Understanding the environmental transformation of multiwall carbon nanotubes (MWCNTs) is important to their life cycle assessment and potential environmental impacts. We report that a bacterial community is capable of degrading 14 C-labeled MWCNTs into 14 CO 2 in the presence of an external carbon source via co-metabolism. Multiple intermediate products were detected, and genotypic characterization revealed three possible microbial degraders: Burkholderia kururiensis, Delftia acidovorans, and Stenotrophomonas maltophilia. This result suggests that microbe/MWCNTs interaction may impact the long-term fate of MWCNTs. Highlights: •Mineralization of MWCNTs by a bacterial community was observed. •The mineralization required an external carbon source. •Multiple intermediate products were identified in the MWCNT degrading culture. •Three bacterial species were found likely responsible for MWCNT degradation. -- The 14 C-labeled multiwall carbon nanotubes can be degraded to 14 CO 2 and other byproducts by a bacteria community under natural conditions

  10. Carbon monoxide

    Energy Technology Data Exchange (ETDEWEB)

    NONE

    1994-12-31

    The document identifies the main sources of carbon monoxide (CO) in the general outdoor atmosphere, describes methods of measuring and monitoring its concentration levels in the United Kingdom, and discusses the effects of carbon monoxide on human health. Following its review, the Panel has put forward a recommendation for an air quality standard for carbon monoxide in the United Kingdom of 10 ppm, measured as a running 8-hour average. The document includes tables and graphs of emissions of CO, in total and by emission source, and on the increase in blood levels of carboxyhaemoglobin with continuing exposure to CO. 11 refs., 4 figs., 4 tabs.

  11. 14C Accelerator mass spectrometry in Brazil

    International Nuclear Information System (INIS)

    Macario, K.D.; Gomes, P.R.S.; Anjos, Roberto M.; Linares, R.; Queiroz, E.A.; Oliveira, F.M.; Cardozo, L.; Carvalho, C.R.A.

    2011-01-01

    Radiocarbon Accelerator Mass Spectrometry is an ultra-sensitive technique that enables the direct measurement of carbon isotopes in samples as small as a few milligrams. The possibility of dating or tracing rare or even compound specific carbon samples has application in many fields of science such as Archaeology, Geosciences and Biomedicine. Several kinds of material such as wood, charcoal, carbonate and bone can be chemically treated and converted to graphite to be measured in the accelerator system. The Physics Institute of Universidade Federal Fluminense (UFF), in Brazil will soon be able to perform the complete 14 C-AMS measurement of samples. At the Nuclear Chronology Laboratory (LACRON) samples are prepared and converted to carbon dioxide. A stainless steel vacuum system was constructed for carbon dioxide purification and graphitization is performed in sealed tubes in a muffle oven. Graphite samples will be analyzed in a 250 kV Single Stage Accelerator produced by National Electrostatic Corporation which will be installed in the beginning of 2012. With the sample preparation laboratory at LACRON and the SSAMS system, the Physics Institute of UFF will be the first 14 C-AMS facility in Latin America. (author)

  12. Calcium Carbonate

    Science.gov (United States)

    ... Calcium is needed by the body for healthy bones, muscles, nervous system, and heart. Calcium carbonate also ... to your pharmacist or contact your local garbage/recycling department to learn about take-back programs in ...

  13. Synthesis of carbon-14 and carbon-13 labelled (R)-(-)2[[4-(2,6-di-1-pyrrolidinyl-4-pyrimidinyl)-1-piperazinyl]me thyl]-3,4-dihydro-2,5,7,8-tetramethyl-2H-1-benzopyran-6-ol. [Anti-asthmatic

    Energy Technology Data Exchange (ETDEWEB)

    Ackland, M.J.; Howard, M.R.; Dring, L.G. (Upjohn Laboratories-Europe, Upjohn Ltd., Crawley (United Kingdom)); Jacobsen, E.J.; Secreast, S.L. (Upjohn Co., Kalamazoo, MI (United States))

    1993-01-01

    This paper describes the synthesis and characterisation of 2[[4-(2,6-di-1-pyrrolidinyl-4-pyrimidinyl)-1-piperazinyl]-[[sup 14]C -methyl]-3,4-dihydro-2,5,7,8-tetramethyl-2H-1-benzopyran-6-ol and 2[[4-(2,6-di-1-pyrrolidinyl-4-[[sup 13]C[sub 2

  14. Infiltrated carbon foam composites

    Science.gov (United States)

    Lucas, Rick D. (Inventor); Danford, Harry E. (Inventor); Plucinski, Janusz W. (Inventor); Merriman, Douglas J. (Inventor); Blacker, Jesse M. (Inventor)

    2012-01-01

    An infiltrated carbon foam composite and method for making the composite is described. The infiltrated carbon foam composite may include a carbonized carbon aerogel in cells of a carbon foam body and a resin is infiltrated into the carbon foam body filling the cells of the carbon foam body and spaces around the carbonized carbon aerogel. The infiltrated carbon foam composites may be useful for mid-density ablative thermal protection systems.

  15. Total synthesis of (7- sup 14 C)-(+-)-colchicine

    Energy Technology Data Exchange (ETDEWEB)

    Pontikis, Renee; Nguyenhoang Nam; Hoellinger, Henri (Paris-5 Univ., 75 (France). Lab. de Chimie et Biochimie Pharmacologiques et Toxicologiques)

    1989-08-01

    The synthesis of ({plus minus})-colchicine labelled with carbon-14 at the 7-position of the B ring was achieved by a sixteen step sequence with an overall radiochemical yield of 2.5% from (Ba{sup 14}CO{sub 3}) (Specific activity: 55 mCi-mmol{sup -1}). (author).

  16. Total synthesis of [7-14C]-(+-)-colchicine

    International Nuclear Information System (INIS)

    Pontikis, Renee; Nguyenhoang Nam; Hoellinger, Henri

    1989-01-01

    The synthesis of (±)-colchicine labelled with carbon-14 at the 7-position of the B ring was achieved by a sixteen step sequence with an overall radiochemical yield of 2.5% from [Ba 14 CO 3 ] (Specific activity: 55 mCi-mmol -1 ). (author)

  17. Increased topsoil carbon stock across China's forests.

    Science.gov (United States)

    Yang, Yuanhe; Li, Pin; Ding, Jinzhi; Zhao, Xia; Ma, Wenhong; Ji, Chengjun; Fang, Jingyun

    2014-08-01

    Biomass carbon accumulation in forest ecosystems is a widespread phenomenon at both regional and global scales. However, as coupled carbon-climate models predicted, a positive feedback could be triggered if accelerated soil carbon decomposition offsets enhanced vegetation growth under a warming climate. It is thus crucial to reveal whether and how soil carbon stock in forest ecosystems has changed over recent decades. However, large-scale changes in soil carbon stock across forest ecosystems have not yet been carefully examined at both regional and global scales, which have been widely perceived as a big bottleneck in untangling carbon-climate feedback. Using newly developed database and sophisticated data mining approach, here we evaluated temporal changes in topsoil carbon stock across major forest ecosystem in China and analysed potential drivers in soil carbon dynamics over broad geographical scale. Our results indicated that topsoil carbon stock increased significantly within all of five major forest types during the period of 1980s-2000s, with an overall rate of 20.0 g C m(-2) yr(-1) (95% confidence interval, 14.1-25.5). The magnitude of soil carbon accumulation across coniferous forests and coniferous/broadleaved mixed forests exhibited meaningful increases with both mean annual temperature and precipitation. Moreover, soil carbon dynamics across these forest ecosystems were positively associated with clay content, with a larger amount of SOC accumulation occurring in fine-textured soils. In contrast, changes in soil carbon stock across broadleaved forests were insensitive to either climatic or edaphic variables. Overall, these results suggest that soil carbon accumulation does not counteract vegetation carbon sequestration across China's forest ecosystems. The combination of soil carbon accumulation and vegetation carbon sequestration triggers a negative feedback to climate warming, rather than a positive feedback predicted by coupled carbon-climate models

  18. Measurement of C-14 distribution in forest around nuclear facilities

    International Nuclear Information System (INIS)

    Atarashi-Andoh, Mariko; Amano, Hikaru; Arakhatoon, Jahan

    2003-01-01

    A simple analytical method of C-14 measurement using fast bomb combustion and liquid scintillation counting (LSC) has been developed for measuring C-14 distribution in the terrestrial environment. Specific activities of C-14 in cedar leaves and soils collected from an area around nuclear facilities and control areas were measured using this method. Depth distribution of Cs-137 in soils was also measured at the same sampling sites and compared with the depth distribution of C-14. C-14 specific activity in cedar leaves examined around nuclear facilities exceeded that in the control areas by 8 to 30 mBq (g carbon) -1 . The depth distribution of C-14 in forest soil shows that C-14 has peak values in the top 10 cm of the soil profiles ascribed to the highest bomb C-14 level in the 1960's. The data were made available to assess the behavior of fallout C-14 in the surface environment. (author)

  19. Carbon sequestration.

    Science.gov (United States)

    Lal, Rattan

    2008-02-27

    Developing technologies to reduce the rate of increase of atmospheric concentration of carbon dioxide (CO2) from annual emissions of 8.6PgCyr-1 from energy, process industry, land-use conversion and soil cultivation is an important issue of the twenty-first century. Of the three options of reducing the global energy use, developing low or no-carbon fuel and sequestering emissions, this manuscript describes processes for carbon (CO2) sequestration and discusses abiotic and biotic technologies. Carbon sequestration implies transfer of atmospheric CO2 into other long-lived global pools including oceanic, pedologic, biotic and geological strata to reduce the net rate of increase in atmospheric CO2. Engineering techniques of CO2 injection in deep ocean, geological strata, old coal mines and oil wells, and saline aquifers along with mineral carbonation of CO2 constitute abiotic techniques. These techniques have a large potential of thousands of Pg, are expensive, have leakage risks and may be available for routine use by 2025 and beyond. In comparison, biotic techniques are natural and cost-effective processes, have numerous ancillary benefits, are immediately applicable but have finite sink capacity. Biotic and abiotic C sequestration options have specific nitches, are complementary, and have potential to mitigate the climate change risks.

  20. Organic compounds preparation with 14 C

    International Nuclear Information System (INIS)

    Shirvani, Gholam Hossein.

    1996-09-01

    Active urea is a basic reagent for the synthesis of active uric-8- 14 C acid. In our manner, activated Barium carbonate with specified activity was placed in a special furnace with ability of passing gases. Then, ammonia gas was passed through it at about 850 Degree C to obtain Barium Cyanamide. Reaction of the produced compound with CO 2 , and then acidification of the mixture, gave activated urea. Condensation of the urea with Ethylcyanoacetate, produce 6-Aminouracil which upon nitrosation, reduction and then condensation with urea, the desired Uric-8- 14 C acid was synthesized. (author). 148 refs.,

  1. 14C Behaviour in PWR coolant

    International Nuclear Information System (INIS)

    Sims, Howard; Dickinson Shirley; Garbett, Keith

    2012-09-01

    Although 14 C is produced in relatively small amounts in PWR coolant, it is important to know its fate, for example whether it is released by gaseous discharge, removed by absorption on ion exchange (IX) resins or deposited on the fuel pin surfaces. 14 C can exist in a range of possible chemical forms: inorganic carbon compounds (probably mainly CO 2 ), elemental carbon, and organic compounds such as hydrocarbons. This paper presents results from a preliminary survey of the possible reactions of 14 C in PWR coolant. The main conclusions of the study are: - A combination of thermal and radiolytic reactions controls the chemistry of 14 C in reactor coolant. A simple chemical kinetic model predicts that CH 3 OH would be the initial product from radiolytic reactions of 14 C following its formation from 17 O. CH 3 OH is predicted to arise as a result of reactions of OH . with CH 4 and CH 3 , and it persists because there is no known radiation chemical reduction mechanism. - Thermodynamic considerations show that CH 3 OH can be thermally reduced to CH 4 in PWR conditions, although formation of CO 2 from small organics is the most thermodynamically favourable outcome. Such reactions could be catalysed on active nickel surfaces in the primary circuit. - Limited plant data would suggest that CH 4 is the dominant form in PWR and CO 2 in BWR. This implies that radiation chemistry may be important in determining the speciation. - Addition of acetate does not affect the amount of 14 C formed, but the addition of large amounts of stable carbon would lead to a large range of additional products, some of which would be expected to deposit on fuel pin surfaces as high molecular weight hydrocarbons. However, the subsequent thermal decomposition reactions of these products are not known. - Acetate addition may represent a small input of 12 C compared with organic material released from CVCS resins, although the importance of this may depend on whether that is predominantly soluble

  2. Isotopic fractionation between organic carbon and carbonate carbon in Precambrian banded ironstone series from Brazil

    International Nuclear Information System (INIS)

    Schidlowski, M.; Eichmann, R.; Fiebiger, W.

    1976-01-01

    37 delta 13 Csub(org) and 9 delta 13 Csub(carb) values furnished by argillaceous and carbonate sediments from the Rio das Velhas and Minas Series (Minas Gerais, Brazil) have yielded means of -24.3 +- 3.9 promille [PDB] and -0.9 +- 1.4 promille [PDB], respectively. These results, obtained from a major sedimentary banded ironstone province with an age between 2 and 3 x 10 9 yr, support previous assumptions that isotopic fractionation between inorganic and organic carbon in Precambrian sediments is about the same as in Phanerozoic rocks. This is consistent with a theoretically expected constancy of the kinetic fractionation factor governing biological carbon fixation and, likewise, with a photosynthetic pedigree of the reduced carbon fraction of Precambrian rocks. (orig.) [de

  3. Metabolism of [2-14C]acetate and its use in assessing hepatic Krebs cycle activity and gluconeogenesis

    International Nuclear Information System (INIS)

    Schumann, W.C.; Magnusson, I.; Chandramouli, V.; Kumaran, K.; Wahren, J.; Landau, B.R.

    1991-01-01

    To examine the fate of the carbons of acetate and to evaluate the usefulness of labeled acetate in assessing intrahepatic metabolic processes during gluconeogenesis, [2-14C]acetate, [2-14C]ethanol, and [1-14C]ethanol were infused into normal subjects fasted 60 h and given phenyl acetate. Distributions of 14C in the carbons of blood glucose and glutamate from urinary phenylacetylglutamine were determined. With [2-14C]acetate and [2-14C]ethanol, carbon 1 of glucose had about twice as much 14C as carbon 3. Carbon 2 of glutamate had about twice as much 14C as carbon 1 and one-half to one-third as much as carbon 4. There was only a small amount in carbon 5. These distributions are incompatible with the metabolism of [2-14C]acetate being primarily in liver. Therefore, [2-14C]acetate cannot be used to study Krebs cycle metabolism in liver and in relationship to gluconeogenesis, as has been done. The distributions can be explained by: (a) fixation of 14CO2 from [2-14C]acetate in the formation of the 14C-labeled glucose and glutamate in liver and (b) the formation of 14C-labeled glutamate in a second site, proposed to be muscle. [1,3-14C]Acetone formation from the [2-14C]acetate does not contribute to the distributions, as evidenced by the absence of 14C in carbons 2-4 of glutamate after [1-14C]ethanol administration

  4. Water-carbon Links in a Tropical Forest: How Interbasin Groundwater Flow Affects Carbon Fluxes and Ecosystem Carbon Budgets

    Energy Technology Data Exchange (ETDEWEB)

    Genereux, David [North Carolina State Univ., Raleigh, NC (United States); Osburn, Christopher [North Carolina State Univ., Raleigh, NC (United States); Oberbauer, Steven [Florida Intl Univ., Miami, FL (United States); Oviedo Vargas, Diana [North Carolina State Univ., Raleigh, NC (United States); Dierick, Diego [Florida Intl Univ., Miami, FL (United States)

    2017-03-27

    This report covers the outcomes from a quantitative, interdisciplinary field investigation of how carbon fluxes and budgets in a lowland tropical rainforest are affected by the discharge of old regional groundwater into streams, springs, and wetlands in the forest. The work was carried out in a lowland rainforest of Costa Rica, at La Selva Biological Station. The research shows that discharge of regional groundwater high in dissolved carbon dioxide represents a significant input of carbon to the rainforest "from below", an input that is on average larger than the carbon input "from above" from the atmosphere. A stream receiving discharge of regional groundwater had greatly elevated emissions of carbon dioxide (but not methane) to the overlying air, and elevated downstream export of carbon from its watershed with stream flow. The emission of deep geological carbon dioxide from stream water elevates the carbon dioxide concentrations in air above the streams. Carbon-14 tracing revealed the presence of geological carbon in the leaves and stems of some riparian plants near streams that receive inputs of regional groundwater. Also, discharge of regional groundwater is responsible for input of dissolved organic matter with distinctive chemistry to rainforest streams and wetlands. The discharge of regional groundwater in lowland surface waters has a major impact on the carbon cycle in this and likely other tropical and non-tropical forests.

  5. Carbon in high-purity germanium

    International Nuclear Information System (INIS)

    Haller, E.E.; Hansen, W.L.; Luke, P.; McMurray, R.; Jarrett, B.

    1981-10-01

    Using 14 C-spiked pyrolytic graphite-coated quartz crucibles for the growth of nine ultra-pure germanium single crystals, we have determined the carbon content and distribution in these crystals. Using autoradiography, we observe a rapidly decreasing carbon cluster concentration in successively grown crystals. Nuclear radiation detectors made from the crystals measure the betas from the internally decaying 14 C nuclei with close to 100% efficiency. An average value for the total carbon concentration [ 14 C + 12 C] is approx. 2 x 10 14 cm -3 , a value substantially larger than expected from earlier metallurgical studies. Contrary to the most recent measurement, we find the shape of the beta spectrum to agree very well with the statistical shape predicted for allowed transitions

  6. Bilan CarboneR - Implementation

    International Nuclear Information System (INIS)

    Wolff, Aurelie

    2015-01-01

    Bilan Carbone TM , a method for calculating greenhouse gas emissions, was developed to help companies and territorial authorities estimate emissions from their activities or on their territories. After validating the audit perimeter and determining the emission categories to be taken into account, activity data is collected and greenhouse gas emissions are calculated using the tool. Besides accounting greenhouse gas emissions at any given time, the inventory evaluates impact on climate and energy dependence. This helps organizations deal with their emissions by classifying them, implementing action plans to reduce emissions and starting a dynamic process taking into account carbon in their strategic decisions

  7. Carbon dioxide and future climate

    Energy Technology Data Exchange (ETDEWEB)

    Mitchell, J M

    1977-03-01

    The addition of carbon dioxide to the atmosphere due to burning fossil fuel is discussed. The release rate of carbon dioxide has been growing since at least 1950 at an average rate of 4.3% per year. If all known fossil fuel reserves in the world are consumed, a total of between 5 and 14 times the present amount of carbon dioxide in the atmosphere will be released. The oceans would then be unlikely to withdraw the proportion of perhaps 40% which they are believed to have withdrawn up to the present. The increase in the atmosphere would be in excess of 3 times or conceivably ten times the present amount. If the reserves are used up within a few hundred years, more than half the excess carbon dioxide would remain in the atmosphere after a thousand years. The ''greenhouse'' effect of carbon dioxide is explained. The simulation with numerical models of the effects of carbon dioxide on atmospheric radiation fluxes is discussed. An estimated increase in the average annual temperature of the earth of 2.4 to 2.9C is given for doubling the carbon dioxide content; also a 7% increase in global average precipitation. The effect of increasing carbon dioxide on global mean temperature is viewed in the perspective of the glacial-interglacial cycles. The warming effect of carbon dioxide may induce a ''super-interglacial'' on the present interglacial which is expected to decline toward a new ice age in the next several thousand years. Finally it is proposed that it may be necessary to phase out the use of fossil fuels before all the knowledge is acquired which would necessitate such an action.

  8. Carbon isotopes of dissolved inorganic carbon reflect utilization of different carbon sources by microbial communities in two limestone aquifer assemblages

    Directory of Open Access Journals (Sweden)

    M. E. Nowak

    2017-08-01

    Full Text Available Isotopes of dissolved inorganic carbon (DIC are used to indicate both transit times and biogeochemical evolution of groundwaters. These signals can be complicated in carbonate aquifers, as both abiotic (i.e., carbonate equilibria and biotic factors influence the δ13C and 14C of DIC. We applied a novel graphical method for tracking changes in the δ13C and 14C of DIC in two distinct aquifer complexes identified in the Hainich Critical Zone Exploratory (CZE, a platform to study how water transport links surface and shallow groundwaters in limestone and marlstone rocks in central Germany. For more quantitative estimates of contributions of different biotic and abiotic carbon sources to the DIC pool, we used the NETPATH geochemical modeling program, which accounts for changes in dissolved ions in addition to C isotopes. Although water residence times in the Hainich CZE aquifers based on hydrogeology are relatively short (years or less, DIC isotopes in the shallow, mostly anoxic, aquifer assemblage (HTU were depleted in 14C compared to a deeper, oxic, aquifer complex (HTL. Carbon isotopes and chemical changes in the deeper HTL wells could be explained by interaction of recharge waters equilibrated with post-bomb 14C sources with carbonates. However, oxygen depletion and δ13C and 14C values of DIC below those expected from the processes of carbonate equilibrium alone indicate considerably different biogeochemical evolution of waters in the upper aquifer assemblage (HTU wells. Changes in 14C and 13C in the upper aquifer complexes result from a number of biotic and abiotic processes, including oxidation of 14C-depleted OM derived from recycled microbial carbon and sedimentary organic matter as well as water–rock interactions. The microbial pathways inferred from DIC isotope shifts and changes in water chemistry in the HTU wells were supported by comparison with in situ microbial community structure based on 16S rRNA analyses. Our findings

  9. Abundant pre-industrial carbon detected in Canadian Arctic headwaters: implications for the permafrost carbon feedback

    Science.gov (United States)

    Dean, J. F.; van der Velde, Y.; Garnett, M. H.; Dinsmore, K. J.; Baxter, R.; Lessels, J. S.; Smith, P.; Street, L. E.; Subke, J.-A.; Tetzlaff, D.; Washbourne, I.; Wookey, P. A.; Billett, M. F.

    2018-03-01

    Mobilization of soil/sediment organic carbon into inland waters constitutes a substantial, but poorly-constrained, component of the global carbon cycle. Radiocarbon (14C) analysis has proven a valuable tool in tracing the sources and fate of mobilized carbon, but aquatic 14C studies in permafrost regions rarely detect ‘old’ carbon (assimilated from the atmosphere into plants and soil prior to AD1950). The emission of greenhouse gases derived from old carbon by aquatic systems may indicate that carbon sequestered prior to AD1950 is being destabilized, thus contributing to the ‘permafrost carbon feedback’ (PCF). Here, we measure directly the 14C content of aquatic CO2, alongside dissolved organic carbon, in headwater systems of the western Canadian Arctic—the first such concurrent measurements in the Arctic. Age distribution analysis indicates that the age of mobilized aquatic carbon increased significantly during the 2014 snow-free season as the active layer deepened. This increase in age was more pronounced in DOC, rising from 101-228 years before sampling date (a 120%-125% increase) compared to CO2, which rose from 92-151 years before sampling date (a 59%-63% increase). ‘Pre-industrial’ aged carbon (assimilated prior to ~AD1750) comprised 15%-40% of the total aquatic carbon fluxes, demonstrating the prevalence of old carbon to Arctic headwaters. Although the presence of this old carbon is not necessarily indicative of a net positive PCF, we provide an approach and baseline data which can be used for future assessment of the PCF.

  10. HLA-B*14

    DEFF Research Database (Denmark)

    Leitman, Ellen M.; Willberg, Christian B.; Tsai, Ming Han

    2017-01-01

    Immune control of human immunodeficiency virus type 1 (HIV) infection is typically associated with effective Gag-specific CD8+ T-cell responses. We here focus on HLA-B*14, which protects against HIV disease progression, but the immunodominant HLA-B*14-restricted anti-HIV response is Env specific...... higher functional avidity (P associated protection against HIV disease progression...... is significantly greater for HLA-B*14:02 than for HLA-B*14:01, consistent with the superior antiviral efficacy of the HLA-B*14-EL9 response. Thus, although Gag-specific CD8+ T-cell responses may usually have greater anti-HIV efficacy, factors independent of protein specificity, including functional avidity...

  11. 14C analysis via intracavity optogalvanic spectroscopy

    International Nuclear Information System (INIS)

    Murnick, Daniel; Dogru, Ozgur; Ilkmen, Erhan

    2010-01-01

    A new ultra sensitive laser-based analytical technique, intracavity optogalvanic spectroscopy (ICOGS), allowing extremely high sensitivity for detection of 14 C-labeled carbon dioxide has recently been demonstrated. Capable of replacing accelerator mass spectrometers (AMS) for many applications, the technique quantifies zeptomoles of 14 C in sub micromole CO 2 samples. Based on the specificity of narrow laser resonances coupled with the sensitivity provided by standing waves in an optical cavity, and detection via impedance variations, limits of detection near 10 -1514 C/ 12 C ratios have been obtained with theoretical limits much lower. Using a 15 W 14 CO 2 laser, a linear calibration with samples from 5 x 10 -15 to >1.5 x 10 -12 in 14 C/ 12 C ratios, as determined by AMS, was demonstrated. Calibration becomes non-linear over larger concentration ranges due to interactions between CO 2 and buffer gas, laser saturation effects and changes in equilibration time constants. The instrument is small (table top), low maintenance and can be coupled to GC or LC input. The method can also be applied to detection of other trace entities. Possible applications include microdosing studies in drug development, individualized sub-therapeutic tests of drug metabolism, carbon dating and real time monitoring of atmospheric radiocarbon.

  12. Radiolytic decomposition of organic C-14 released from TRU waste

    International Nuclear Information System (INIS)

    Kani, Yuko; Noshita, Kenji; Kawasaki, Toru; Nishimura, Tsutomu; Sakuragi, Tomofumi; Asano, Hidekazu

    2007-01-01

    It has been found that metallic TRU waste releases considerable portions of C-14 in the form of organic molecules such as lower molecular weight organic acids, alcohols and aldehydes. Due to the low sorption ability of organic C-14, it is important to clarify the long-term behavior of organic forms under waste disposal conditions. From investigations on radiolytic decomposition of organic carbon molecules into inorganic carbonic acid, it is expected that radiation from TRU waste will decompose organic C-14 into inorganic carbonic acid that has higher adsorption ability into the engineering barriers. Hence we have studied the decomposition behavior of organic C-14 by gamma irradiation experiments under simulated disposal conditions. The results showed that organic C-14 reacted with OH radicals formed by radiolysis of water, to produce inorganic carbonic acid. We introduced the concept of 'decomposition efficiency' which expresses the percentage of OH radicals consumed for the decomposition reaction of organic molecules in order to analyze the experimental results. We estimated the effect of radiolytic decomposition on the concentration of organic C-14 in the simulated conditions of the TRU disposal system using the decomposition efficiency, and found that the concentration of organic C-14 in the waste package will be lowered when the decomposition of organic C-14 by radiolysis was taken into account, in comparison with the concentration of organic C-14 without radiolysis. Our prediction suggested that some amount of organic C-14 can be expected to be transformed into the inorganic form in the waste package in an actual system. (authors)

  13. Production of carbon 14-labeled fumonisin in liquid culture

    Energy Technology Data Exchange (ETDEWEB)

    Blackwell, B. A.; Miller, J. D.; Savard, M. E.

    1994-03-15

    Currently, fumonisin B{sub 1} is obtained primarily by using solid culture methods. Although fumonisin B{sub 1} concentrations obtained in solid culture are typically quite high, subsequent extraction and purification present problems. In addition, current methods utilize complex media which makes analysis of biosynthetic pathways and control mechanisms difficult. Liquid culture methods of production could eliminate many problems associated with production in solid culture. However, in the past, concentrations obtained in liquid culture have been relatively low. In this work, factors affecting the production of fumonisin B{sub 1} from a shake flask scale of 100 ml to a fermenter scale of 100 liters were examined. Best results were obtained by using a fed batch method that is nitrogen limited, with pH control. With this method, concentrations in excess of 1000 ppm can be obtained. (author)

  14. Production of carbon 14-labeled fumonisin in liquid culture

    International Nuclear Information System (INIS)

    Blackwell, B.A.; Miller, J.D.; Savard, M.E.

    1994-01-01

    Currently, fumonisin B 1 is obtained primarily by using solid culture methods. Although fumonisin B 1 concentrations obtained in solid culture are typically quite high, subsequent extraction and purification present problems. In addition, current methods utilize complex media which makes analysis of biosynthetic pathways and control mechanisms difficult. Liquid culture methods of production could eliminate many problems associated with production in solid culture. However, in the past, concentrations obtained in liquid culture have been relatively low. In this work, factors affecting the production of fumonisin B 1 from a shake flask scale of 100 ml to a fermenter scale of 100 liters were examined. Best results were obtained by using a fed batch method that is nitrogen limited, with pH control. With this method, concentrations in excess of 1000 ppm can be obtained. (author)

  15. Carbonizing process

    Energy Technology Data Exchange (ETDEWEB)

    1923-11-22

    In the downward distillation of coal, shale, lignite, or the like, the heat is generated by the combustion of liquid or gaseous fuel above the charge the zone of carbonization thus initiated travelling downwards through the charge. The combustible gases employed are preferably those resulting from the process but gases such as natural gas may be employed. The charge is in a moistened and pervious state the lower parts being maintained at a temperature not above 212/sup 0/F until influenced by contact with the carbonization zone and steam may be admitted to increase the yield of ammonia. The combustible gases may be supplied with insufficient air so as to impart to them a reducing effect.

  16. Radiolysis of Ca14CO3

    International Nuclear Information System (INIS)

    Sanchez, M.G.A.

    1986-01-01

    The partition-ion exclusion chromatography is evaluated to analyse non-ionic organic compounds obtained from radiolysis of high specific activity Ca 14 CO 3 . The Ca 14 CO 3 was irradiated by β - decay of carbon-14 or by γ rays from a cobalt-60 source. The crystals were dissolved for qualitative and quantitative analysis of the radiolytic products. Formic and oxalic acids were produced in high yields. Glyoxylic, acetic and glycolic acids, formaldehyde and methanol were produced in low yields. Quantitative determination was carried out by liquid scintillation spectroscopy and the chemical yields (G-values) were calculated for the products. Mechanisms of product formation are proposed based on thermal annealing experiments. (Author) [pt

  17. Carbon aerogels

    International Nuclear Information System (INIS)

    Berthon-Fabry, S.; Achard, P.

    2003-06-01

    The carbon aerogel is a nano-porous material at open porosity, electrical conductor. The aerogels morphology is variable in function of the different synthesis parameters. This characteristic offers to the aerogels a better adaptability to many applications: electrodes (super condensers, fuel cells). The author presents the materials elaboration and their applications. It provides also the research programs: fundamental research, realization of super-condenser electrodes, fuel cells electrodes, gas storage materials and opaque materials for thermal insulation. (A.L.B.)

  18. Temporal distribution of bomb 14C in a forest soil

    International Nuclear Information System (INIS)

    Harkness, D.D.; Harrison, A.F.; Bacon, P.J.

    1986-01-01

    Patterns of 14 C enrichment in the superficial plant debris and mineral soil horizons of an established woodland have been monitored at regular intervals during the past 15 years. These data are compared with a model evaluation of carbon turnover based on the recorded changes in atmospheric 14 C concentration since AD 1900. Leaf litter and decomposing plant debris are characterized by steady-state turnover values of ca 2 and ca 8 years, respectively. A two-component system of fast (≤20 yr) and slow (ca 350 yr) cycling carbon is indicated for the surface (0-5cm) soil humus; below 10cm, the fast component is rare ( 14 C to the soil carbon pool

  19. Carbon cycle

    Energy Technology Data Exchange (ETDEWEB)

    Jaeger, J; Halbritter, G; Neumann-Hauf, G

    1982-05-01

    This report contains a review of literature on the subjects of the carbon cycle, the increase of the atmospheric CO/sub 2/ concentration and the possible impacts of an increased CO/sub 2/ concentration on the climate. In addition to this survey, the report discusses the questions that are still open and the resulting research needs. During the last twenty years a continual increase of the atmospheric carbon dioxide concentration by about 1-2 ppm per years has been observed. In 1958 the concentration was 315 ppm and this increased to 336 ppm in 1978. A rough estimate shows that the increase of the atmospheric carbon dioxide concentration is about half of the amount of carbon dioxide added to the atmosphere by the combustion of fossil fuels. Two possible sinks for the CO/sub 2/ released into the atmosphere are known: the ocean and the biota. The role of the biota is, however, unclear, since it can act both as a sink and as a source. Most models of the carbon cycle are one-dimensional and cannot be used for accurate predictions. Calculations with climate models have shown that an increased atmospheric CO/sub 2/ concentration leads to a warming of the earth's surface and lower atmosphere. Calculations show that a doubling of the atmospheric CO/sub 2/-concentration would lead to a net heating of the lower atmosphere and earth's surface by a global average of about 4 W m/sup -2/. Greater uncertainties arise in estimating the change in surface temperature resulting from this change in heating rate. It is estimated that the global average annual surface temperature would change between 1.5 and 4.5 K. There are, however, latitudinal and seasonal variations of the impact of increased CO/sub 2/ concentration. Other meteorological variables (e.g. precipitation, wind speed etc.) would also be changed. It appears that the impacts of the other products of fossil fuel combustion are unlikely to counteract the impacts of CO/sub 2/ on the climate.

  20. 14C2H4: distribution of 14C-labeled tissue metabolites in pea seedlings

    International Nuclear Information System (INIS)

    Giaquinta, R.; Beyer, E. Jr.

    1977-01-01

    The 14 C-metabolite distribution pattern following 14 C 2 H 4 metabolism in intact pea seedlings (Pisum sativum L.) was determined under various conditions. After a 24 hr exposure to 14 C 2 H 4 , the majority of 14 C-metabolites were water-soluble (60-70%) with lesser amounts in the protein (10-15%), lipid (1%), and insoluble (1-2%) fractions. Ion exchange chromatography of the water-soluble components into basic, neutral, and acidic fractions revealed a 50:40:10 distribution, respectively. Chromatography of the neutral fraction revealed two regions of radioactivity (Rf=0.38) and 0.63 which did not cochromatograph with twenty-two known sugars or neutral metabolites. Chromatograms of the basic fraction contained 3 regions of radioactivity. Similar distribution patterns were noted when 14 C 2 H 4 exposure was followed by a 6 hr air chase or when 5% CO 2 , an antagonist of ethylene action, was present during the exposure. Marked differences in the 14 C-metabolite distribution patterns were obtained when 14 CO 2 was substituted for 14 C 2 H 4 . These results indicate that the metabolic pathway involved in ethylene metabolism is different from that involved in intermediately carbon metabolism. (auth.)

  1. Analysis of 14C level around Qinshan NPP base

    International Nuclear Information System (INIS)

    Huang Renjie; Liang Haiyan; Chen Qianyuan; Ni Shiying; He Jun; Zeng Guangjian; Ma Yongfu

    2012-01-01

    By using the method of alkaline solution absorption, the activity concentrations of Carbon-14 as well as its variation tendency in air and biological samples were analyzed. The air samples and biological samples were collected around the Qinshan nuclear power plant base (Qinshan NPP Base) in 2002 to 2009 and 2007 to 2009 respectively. The results showed that, since 2002, the annual average activity concentrations of Carbon-14 in air samples were in the range of 38.3 mBq/m 3 to 55.4 mBq/m 3 . Although the monitoring results of Xiajiawan village and Yanliucun village were comparatively higher than the reference site in Hangzhou City, the results were still at the same level. Meanwhile, monitoring results of Xiajiawan village and Yangliucun village in the summer of 2004 and 2005 are relatively high, with the peak value of 55.4 mBq/m 3 appeared in Xiajiawan village during the summer of 2005. Correspondingly the annual airborne Carbon-14 of 2004 and 2005 discharged from the Qinshan NPP 3 rd Phase were higher than normal as well, it can therefore be concluded that the activity concentration of Carbon-14 around the Qinshan NPP Base are related to the discharged source term. The activity concentration of Carbon-14 in rice and leaf vegetable samples from Xiajiawan village and Yangliucun village were slightly higher, but within the same level, than that of Hangzhou. The activity concentration of Carbon-14 in the mullet samples collected from the sea area around Qinshan NPP Base are approximately the same with the sea area of Zhoushan. (authors)

  2. Processing ix spent resin waste for C-14 isotope recovery

    International Nuclear Information System (INIS)

    Chang, F. H.; Woodall, K. B.; Sood, S. K.; Vogt, H. K.; Krochmainek, L. S.

    1991-01-01

    A process developed at Ontario Hydro for recovering carbon-14 (C-14) from spent ion exchange resin wastes is described. Carbon-14 is an undesirable by-product of CANDU 1 nuclear reactor operation. It has an extremely long (5730 years) half-life and can cause dosage to inhabitants by contact, inhalation, or through the food cycle via photosynthesis. Release of carbon-14 to the environment must be minimized. Presently, all the C-14 produced in the Moderator and Primary Heat Transport (PHT) systems of the reactor is effectively removed by the respective ion exchange columns, and the spent ion exchange resins are stored in suitably engineered concrete structures. Because of the large volumes of spent resin waste generated each year this method of disposal by long term storage tends to be uneconomical; and may also be unsatisfactory considering the long half-life of the C-14. However, purified C-14 is a valuable commercial product for medical, pharmaceutical, agricultural, and organic chemistry research. Currently, commercial C-14 is made artificially in research reactors by irradiating aluminum nitride targets for 4.5 years. If the C-14 containing resin waste can be used to reduce this unnecessary production of C-14, the total global build-up of this radioactive chemical can be reduced. There is much incentive in removing the C-14 from the resin waste to reduce the volume of C-14 waste, and also in purifying the recovered C-14 to supply the commercial market. The process developed by Ontario Hydro consists of three main steps: C-14 removal from spent resins, enrichment of recovered C-14, and preparation of final product. Components of the process have been successfully tested at Ontario Hydro's Research Division, but the integration of the process is yet to be demonstrated. A pilot scale plant capable of processing 4 m 3 of spent resins annually is being planned for demonstrating the technology. The measured C-14 activity levels on the spent resins ranged from 47

  3. The carbon-sequestration potential of a global afforestation program

    International Nuclear Information System (INIS)

    Nilsson, S.; Schopfhauser, W.

    1995-01-01

    The authors analyzed the changes in the carbon cycle that could be achieved with a global large-scale afforestation program that is economically, politically and technically feasible. They estimated that of the areas regarded as suitable for large-scale plantations, only about 345 million ha would actually be available for plantations and agroforestry for the sole purpose of sequestering carbon. The maximum annual rate of carbon fixation (1.48 Gt/yr) would only be achieved 60 years after the establishment of the plantation - 1.14 Gt by above-ground biomass and 0.34 Gt by below-ground biomass. Over the periods from 1995 to 2095, a total of 104 Gt of carbon would be sequestered. This is substantially lower than the amount of carbon required to offset current carbon emissions (3.8 Gt/yr) in order to stabilize the carbon content of the atmosphere. 108 refs., 1 fig., 14 tabs

  4. Radiocarbon C-14 dating - MINT experience

    International Nuclear Information System (INIS)

    Kamisah Alias

    2002-01-01

    The measurement of a radiocarbon date is a complex process which involved all the stages from advice given prior to submission of samples right through to reporting of results. The aim of our radiocarbon dating is to determine the residual 14 C content of a sample, the value of which is translated into an age that is an estimate of the time elapsed since the given sample was removed from the environment in which it had formed in equilibrium with respect to 14-C radioactive decay and metabolic assimilation. Carbon is obtained from carbon containing samples in the form of carbon dioxide, which is then reacted with lithium forming lithium carbide. The carbide is then hydrolysed to acetylene before it was polymerised to benzene using a high-efficiency vanadium-alumina-silica catalyst to produce benzene with up to 96% yield. Sample, background and modem standard activities are measured with a coincidence scintillation counter using in glass vials of 21 ml capacity. An improved chemical procedure was used to obtain and purify the benzene from the samples for measurement using a liquid scintillation counter. Radiocarbon dating measurements of samples collected reveal some results. The validity of the data have yet to be confirmed by the results of the measurements on two international control samples. (Author)

  5. Carbons and carbon supported catalysts in hydroprocessing

    Energy Technology Data Exchange (ETDEWEB)

    Furimsky, Edward

    2009-07-01

    This book is a comprehensive summary of recent research in the field and covers all areas of carbons and carbon materials. The potential application of carbon supports, particularly those of carbon black (CB) and activated carbon (AC) in hydroprocessing catalysis are covered. Novel carbon materials such as carbon fibers and carbon nano tubes (CNT) are also covered, including the more recent developments in the use of fullerenes in hydroprocessing applications. Although the primary focus of this book is on carbons and carbon supported catalysts, it also identifies the difference in the effect of carbon supports compared with the oxidic supports, particularly that of the Al{sub 2}O{sub 3}. The difference in catalyst activity and stability was estimated using both model compounds and real feeds under variable conditions. The conditions applied during the preparation of carbon supported catalysts are also comprehensively covered and include various methods of pretreatment of carbon supports to enhance catalyst performance. The model compounds results consistently show higher hydrodesulfurization and hydrodeoxygenation activities of carbon supported catalysts than that of the Al{sub 2}O{sub 3} supported catalysts. Also, the deactivation of the former catalysts by coke deposition was much less evident. Chapter 6.3.1.3 is on carbon-supported catalysts: coal-derived liquids.

  6. 14C Analysis of protein extracts from Bacillus spores.

    Science.gov (United States)

    Cappuccio, Jenny A; Falso, Miranda J Sarachine; Kashgarian, Michaele; Buchholz, Bruce A

    2014-07-01

    Investigators of bioagent incidents or interdicted materials need validated, independent analytical methods that will allow them to distinguish between recently made bioagent samples versus material drawn from the archives of a historical program. Heterotrophic bacteria convert the carbon in their food sources, growth substrate or culture media, into the biomolecules they need. The F(14)C (fraction modern radiocarbon) of a variety of media, Bacillus spores, and separated proteins from Bacillus spores was measured by accelerator mass spectrometry (AMS). AMS precisely measures F(14)C values of biological materials and has been used to date the synthesis of biomaterials over the bomb pulse era (1955 to present). The F(14)C of Bacillus spores reflects the radiocarbon content of the media in which they were grown. In a survey of commercial media we found that the F(14)C value indicated that carbon sources for the media were alive within about a year of the date of manufacture and generally of terrestrial origin. Hence, bacteria and their products can be dated using their (14)C signature. Bacillus spore samples were generated onsite with defined media and carbon free purification and also obtained from archived material. Using mechanical lysis and a variety of washes with carbon free acids and bases, contaminant carbon was removed from soluble proteins to enable accurate (14)C bomb-pulse dating. Since media is contemporary, (14)C bomb-pulse dating of isolated soluble proteins can be used to distinguish between historical archives of bioagents and those produced from recent media. Copyright © 2014 Elsevier Ireland Ltd. All rights reserved.

  7. Carbon classified?

    DEFF Research Database (Denmark)

    Lippert, Ingmar

    2012-01-01

    . Using an actor- network theory (ANT) framework, the aim is to investigate the actors who bring together the elements needed to classify their carbon emission sources and unpack the heterogeneous relations drawn on. Based on an ethnographic study of corporate agents of ecological modernisation over...... a period of 13 months, this paper provides an exploration of three cases of enacting classification. Drawing on ANT, we problematise the silencing of a range of possible modalities of consumption facts and point to the ontological ethics involved in such performances. In a context of global warming...

  8. Carbon Footprints

    OpenAIRE

    Rahel Aichele; Gabriel Felbermayr

    2011-01-01

    Lässt sich der Beitrag eines Landes zum weltweiten Klimaschutz an der Veränderung seines CO2-Ausstoßes messen, wie es im Kyoto-Abkommen implizit unterstellt wird? Oder ist aufgrund der Bedeutung des internationalen Güterhandels der Carbon Footprint – der alle CO2-Emissionen erfasst, die durch die Absorption (d.h. Konsum und Investitionen) eines Landes entstehen – das bessere Maß? Die Autoren erstellen eine Datenbank mit den Footprints von 40 Ländern für den Zeitraum 1995–2007. Die deskriptive...

  9. An enzymic method for the determination of [1-14C] lactose

    International Nuclear Information System (INIS)

    Davies, E.; Bourke, E.; Costello, J.

    1975-01-01

    A simple, rapid and specific method for the determination of [1- 14 C] lactose in biological fluids is described. It is based on the enzymic removal of the 1- 14 C atom of lactose as [ 14 C] carbon dioxide, using commercially available enzymes. The assay involves only one critical addition and the entire reaction can be carried out in a scintillation vial. (author)

  10. Soil carbon dynamics inferred from carbon isotope compositions of soil organic matter and soil respiration

    International Nuclear Information System (INIS)

    Koarashi, Jun; Asano, Tomohiro; Iida, Takao; Moriizumi, Jun

    2004-01-01

    To better understand 14 C cycling in terrestrial ecosystems, 14 C abundances were evaluated for fractionated soil organic matter (SOM) and soil respiration in an urban forest. In 2001 soil profile, Δ 14 C values of litter and bulk SOM increased rapidly from litter surface (62.7 per mille) to uppermost mineral soil layer (244.9 per mille), and then decreased sharply to 6 cm depth of mineral soil (125.0 per mille). Carbon enriched in 14 C by atmospheric nuclear weapons testing had penetrated to at least 16 cm depth of mineral soil. The average Δ 14 C in atmospheric CO 2 was 58.8 per mille in August 2001, suggesting recent carbon input to the topmost litter layer. Although a similar depth distribution was observed for Δ 14 C values of residual SOM after acid hydrolysis, the Δ 14 C values were slightly lower than those in bulk SOM. This indicates input of 'bomb' C into this organic fraction and higher 14 C abundance in acid-soluble SOM. The most of CO 2 may be derived from the microbial decomposition of the acid-soluble, or labile, SOM. Therefore, the labile SOM may become most influential pool for soil carbon cycling. In contrast, carbon in base-insoluble SOM remained considerably low in 14 C abundance at all depths, suggesting no or little incorporation of 'bomb' C to this fraction. Values of Δ 14 C in soil respiration ranged from 91.9 to 146.4 per mille in August 2001, showing a significant contribution from decomposition of SOM fixed over past 2-40 years. These results indicate that the use of bulk SOM as a representative of soil carbon pool would lead to severe misunderstand of the soil C dynamics on decadal and shorter time scales. (author)

  11. Design, Synthesis, and Applications of Carbon Nanohoops

    Science.gov (United States)

    2016-05-23

    rings via one electron reduction reactions was feasible. Therefore, the synthesis and spectroscopic investigations of these ring systems by reducing...Release; Distribution Unlimited UU UU UU UU 23-05-2016 15-Feb-2012 14-Feb-2016 Final Report: Design, Synthesis , and Applications of Carbon Nanohoops The...Office P.O. Box 12211 Research Triangle Park, NC 27709-2211 Caron Nanohoops, paracyclophanes, carbon nanotubes, organic synthesis REPORT

  12. Production of an accelerated oxygen-14 beam

    International Nuclear Information System (INIS)

    Powell, J.; O'Neil, J.P.; Cerny, Joseph

    2003-01-01

    BEARS is an ongoing project to provide a light-ion radioactive-beam capability at the 88-Inch Cyclotron at LBNL. Light radioactive isotopes are produced at a 10 MeV proton medical cyclotron, transported 350 m via a high-speed gas transport capillary, cryogenically separated, and injected into the 88-Inch Cyclotron's ion source. The first radioactive beam successfully accelerated was carbon-11 and beams of intensity more than 10 8 ions/s have been utilized for experiments. Development of oxygen-14 as the second BEARS beam presented considerable technical challenges, both due to its short half-life of 71 s and the radiation chemistry of oxygen in the target. The usual techniques developed for medical uses of oxygen-15 involve the addition of significant amounts of carrier oxygen, something that would overload the ion source. As a solution, oxygen-14 is produced as water in a carrier-free form, and is chemically converted in two steps to carbon dioxide, a form readily usable by the BEARS. This system has been built and is operational, and initial tests of accelerating an oxygen-14 beam have been performed

  13. [Characteristics of carbon storage of Inner Mongolia forests: a review].

    Science.gov (United States)

    Yang, Hao; Hu, Zhong-Min; Zhang, Lei-Ming; Li, Sheng-Gong

    2014-11-01

    Forests in Inner Mongolia account for an important part of the forests in China in terms of their large area and high living standing volume. This study reported carbon storage, carbon density, carbon sequestration rate and carbon sequestration potential of forest ecosystems in Inner Mongolia using the biomass carbon data from the related literature. Through analyzing the data of forest inventory and the generalized allometric equations between volume and biomass, previous studies had reported that biomass carbon storage of the forests in Inner Mongolia was about 920 Tg C, which was 12 percent of the national forest carbon storage, the annual average growth rate was about 1.4%, and the average of carbon density was about 43 t · hm(-2). Carbon storage and carbon density showed an increasing trend over time. Coniferous and broad-leaved mixed forest, Pinus sylvestris var. mongolica forest and Betula platyphylla forest had higher carbon sequestration capacities. Carbon storage was reduced due to human activities such as thinning and clear cutting. There were few studies on carbon storage of the forests in Inner Mongolia with focus on the soil, showing that the soil car- bon density increased with the stand age. Study on the carbon sequestration potential of forest ecosystems was still less. Further study was required to examine dynamics of carbon storage in forest ecosystems in Inner Mongolia, i. e., to assess carbon storage in the forest soils together with biomass carbon storage, to compute biomass carbon content of species organs as 45% in the allometric equations, to build more species-specific and site-specific allometric equations including root biomass for different dominant species, and to take into account the effects of climate change on carbon sequestration rate and carbon sequestration potential.

  14. How accurate is the 14C method

    International Nuclear Information System (INIS)

    Nydal, R.

    1979-01-01

    Radiocarbon daters have in recent years focussed their interest on accuracy and reliability of 14 C dates. The use of dates for resolving fine chronological structures that are not dateable otherwise has stressed this point. The total uncertainty in dating an event is composed of errors relating to dating of the sample, i.e. uncertainty in measured quantities, deviations from assumed content of 14 C in material when alive; and errors related to quality of sample material, i.e. contamination from carbon of different age, diffuse context between sample and event. Statistical variability in counting of 14 C activity gives the most important contribution to measurement uncertainty - increasing with age and shortage of sample material. Corrections for isotopic fractionation and reservoir effects must be performed, and - most important when dates are compared with historical ages - the dendrochronological calibration will correct for past variations in the atmospheric 14 C content. Future improvement of dating precision can however only be obtained by the combined efforts of both daters and submitters of samples, thus minimizing errors related to selection and handling of sample material as well as those related to the 14 C method and measurements. (Auth.)

  15. 14C tebuconazole degradation in Colombian soils.

    Science.gov (United States)

    Mosquera, C S; Martínez, M J; Guerrero, J A

    2010-01-01

    Tebuconazole is a fungicide used on onion crops (Allium Fistulosum L) in Colombia. Persistence of pesticides in soils is characterized by the half-life (DT50), which is influenced by their chemical structure, the physical and chemical properties of the soil and the previous soil history. Based on its structural and chemical properties, tebuconazole should be expected to be relatively persistent in soils. Laboratory incubation studies were conducted to evaluate persistence and bond residues of 14C tebuconazole in three soils, two inceptisol (I) and one histosol (H). Textural classifications were: loam (101), loamy sand (102) and loam (H03), respectively. Data obtained followed a first-order degradation kinetics (R2 > or = 0.899) with DT50 values between 158 and 198 days. The production of 14CO2 from the 14C-ring-labelled test chemicals was very low and increased slightly during 63 days in all cases. The methanol extractable 14C-residues were higher than aqueous ones and both decreased over incubation time for the three soils. The formation of bound 14C-residues increased with time and final values were 11.3; 5.55 and 7.87% for 101, 102 and H03 respectively. Soil 101 showed the lowest mineralization rate and the highest bound residues formation, which might be explained by the clay fraction content. In contrast, an inverse behavior was found for soils 102 and H03, these results might be explained by the higher soil organic carbon content.

  16. Trading forest carbon

    Science.gov (United States)

    The nature of carbon in forests is discussed from the perspective of carbon trading. Carbon inventories, specifically in the area of land use and forestry are reviewed for the Pacific Northwest. Carbon turnover in forests is discussed as it relates to carbon sequestration. Scient...

  17. Carbon dioxide emissions from biochar in soil

    DEFF Research Database (Denmark)

    Bruun, Sander; Clauson-Kaas, Anne Sofie Kjærulff; Bobuľská, L.

    2014-01-01

    The stability of biochar in soil is of importance if it is to be used for carbon sequestration and long-term improvement of soil properties. It is well known that a significant fraction of biochar is highly stable in soil, but carbon dioxide (CO2) is also released immediately after application....... This study investigated the nature of the early release of CO2 and the degree to which stabilizing mechanisms protect biochar from microbial attack. Incubations of 14C-labelled biochar produced at different temperatures were performed in soils with different clay contents and in sterilized and non......-sterilized soils. It emerged that carbonate may be concentrated or form during or after biochar production, resulting in significant carbonate contents. If CO2 released from carbonates in short-term experiments is misinterpreted as mineralization of biochar, the impact of this process may be significantly over...

  18. Apollo 14 emblem

    Science.gov (United States)

    1970-01-01

    This is the Apollo 14 crew patch. It features the astronaut lapel pin approaching the Moon and leaving a comet trail from the liftoff point on Earth. The pin design was adopted by the astronaut corps several years ago. Astronauts who have not yet flown in space wear silver pins. Those who have flown wear gold pins.

  19. Carbon stocks and flux in French forests

    International Nuclear Information System (INIS)

    Dupouey, Jean-Luc; Pignard, Gerome; Badeau, Vincent; Thimonier, A.; Dhote, Jean-Francois; Nepveu, G.; Berges, L.; Augusto, L.; Belkacem, S.; Nys, C.

    2000-01-01

    Forests contain most of the carbon stored in the earth's biomass (81 %) and could play a role in CO 2 mitigation to a certain extent. We estimate French forest carbon stocks in biomass to be 860 MtC on 14.5 million hectares of forests, and 1,140 MtC in forest soils. Total carbon in the 14.5 million hectares of French forests is estimated at 2,000 MtC. Average annual flux for the 1979/91 period is 10.5 MtC/y, i.e. 10 % of national fossil fuel emissions. The main causes of this net carbon uptake are the rapid increase of forest area, increasing productivity due to environmental changes, ageing or, in some localized areas, more intensive silviculture practices. These carbon sinks are not offset by the harvesting level which remains low on average (61 % of the annual volume growth). Forestry carbon mitigation options applicable in France are discussed. The need for global economic and ecological budgets (including carbon stocks, soil fertility and biodiversity) of the possible alternatives is stressed. (authors)

  20. BOREAS TGB-12 Isotropic Carbon Dioxide Data over the NSA

    Science.gov (United States)

    Trumbore, Susan; Hall, Forrest G. (Editor); Sundquist, Eric; Winston, Greg; Conrad, Sara K. (Editor)

    2000-01-01

    The BOREAS TGB-12 team made measurements of soil carbon inventories, carbon concentration in soil gases, and rates of soil respiration at several sites to estimate the rates of carbon accumulation and turnover in each of the major vegetation types. This data set contains information on the carbon isotopic content of carbon dioxide sampled from soils in the NSA-OBS, NSA-YJP, and NSA-OJP sites. Data were collected from 14-Nov-1993 to 10-Oct-1996. The data are stored in tabular ASCII files.

  1. Sources of C-14 generation and associated doses

    International Nuclear Information System (INIS)

    Amado, Valeria A.; Biaggio, Alfredo L.; Canoba, Analia C.; Curti, Adriana R.

    2009-01-01

    C-14 is a radioactive isotope of C with a half-life of 5700 years that decays to N-14 by emission of beta radiation. It is naturally produced in the upper atmosphere by cosmic ray neutrons via the (n;p) reaction over N-14. Anthropogenic C-14 has been generated in the past by atmospheric nuclear weapon tests and it is currently produced during the operation of nuclear reactors. Once released this radionuclide behaves in the biosphere as the standard carbon cycle. Since the beginning of the industrial period the relationship Carbon-14/Stable Carbon has changed continuously, and so the dose incurred by the world population. In this paper the main anthropogenic activities that modified such relationship are presented and analyzed: the Suess effect and the generation of nuclear energy. It is concluded that the current trend of reduction of the total dose due to C-14 will continue during the next decades. Finally it is indicated that in order to prevent an excessive accumulation of this radionuclide in the biosphere, actions should be collectively implemented to be effective. (author) [es

  2. Radio photosynthesis of some 14 C-labelled sugars using the unicellular green alga scenedesmus ACUTUS

    International Nuclear Information System (INIS)

    Barakat, M.F.; Farag, A.N.; Ragab, M.T.; El-Fouly, M.M.; El-Baz, F.K.

    1993-01-01

    Radiosynthesis has been carried out using the unicellular green alga scenedesmus acutus together with Na H 14 CO 3 solution as a carbon-14 source, in an ordinary photosynthesis chamber. The process is more easier and less laborious than the techniques involving the use of gaseous 14 CO 2 in a tight photosynthesis chamber. Uniformly labelled 14 C-glucose, 14 C-fructose and 14 C-sucrose have been prepared with specific activities of several micro curies per milli mole. The specific activity of the products was found to increase on increasing the photosynthesis time or the initial activity of the Na H 14 CO 3 solution used. 3 tabs

  3. Carbon Monoxide Information Center

    Medline Plus

    Full Text Available ... Education Centers Carbon Monoxide Information Center Carbon Monoxide Information Center En Español The Invisible Killer Carbon monoxide, ... Install one and check its batteries regularly. View Information About CO Alarms Other CO Topics Safety Tips ...

  4. Global Carbon Budget 2017

    NARCIS (Netherlands)

    Le Quere, Corinne; Andrew, Robbie M.; Friedlingstein, Pierre; Sitch, Stephen; Pongratz, Julia; Manning, Andrew C.; Korsbakken, Jan Ivar; Peters, Glen P.; Canadell, Josep G.; Jackson, Robert B.; Boden, Thomas A.; Tans, Pieter P.; Andrews, Oliver D.; Arora, Vivek K.; Bakker, Dorothee C. E.; Barbero, Leticia; Becker, Meike; Betts, Richard A.; Bopp, Laurent; Chevallier, Frederic; Chini, Louise P.; Ciais, Philippe; Cosca, Catherine E.; Cross, Jessica; Currie, Kim; Gasser, Thomas; Harris, Ian; Hauck, Judith; Haverd, Vanessa; Houghton, Richard A.; Hunt, Christopher W.; Hurtt, George; Ilyina, Tatiana; Jain, Atul K.; Kato, Etsushi; Kautz, Markus; Keeling, Ralph F.; Goldewijk, Kees Klein; Koertzinger, Arne; Landschuetzer, Peter; Lefevre, Nathalie; Lenton, Andrew; Lienert, Sebastian; Lima, Ivan; Lombardozzi, Danica; Metzl, Nicolas; Millero, Frank; Monteiro, Pedro M. S.; Munro, David R.; Nabel, Julia E. M. S.; Nakaoka, Shin-ichiro; Nojiri, Yukihiro; Padin, X. Antonio; Peregon, Anna; Pfeil, Benjamin; Pierrot, Denis; Poulter, Benjamin; Rehder, Gregor; Reimer, Janet; Roedenbeck, Christian; Schwinger, Jorg; Seferian, Roland; Skjelvan, Ingunn; Stocker, Benjamin D.; Tian, Hanqin; Tilbrook, Bronte; Tubiello, Francesco N.; van der Laan-Luijkx, Ingrid T.; van der Werf, Guido R.; van Heuven, Steven; Viovy, Nicolas; Vuichard, Nicolas; Walker, Anthony P.; Watson, Andrew J.; Wiltshire, Andrew J.; Zaehle, Soenke; Zhu, Dan

    2018-01-01

    Accurate assessment of anthropogenic carbon dioxide (CO2) emissions and their redistribution among the atmosphere, ocean, and terrestrial biosphere - the "global carbon budget" - is important to better understand the global carbon cycle, support the development of climate policies, and project

  5. Carbon Monoxide Information Center

    Medline Plus

    Full Text Available ... Education Safety Education Centers Carbon Monoxide Information Center Carbon Monoxide Information Center En Español The Invisible Killer Carbon monoxide, also known as CO, is called the " ...

  6. Study of the C-14-contamination potential of C-impurities in CuO and Fe

    NARCIS (Netherlands)

    Vandeputte, K; Moens, L; Dams, R; van der Plicht, Johannes

    1998-01-01

    The carbon concentration in CuO and iron was determined by isolating C. The values were in agreement with results reported in other studies. Contaminating carbon from CuO and Fe was transformed to AMS targets and measured for C-14. C-traces in CuO were shown to be the major contribution to the C-14

  7. Carbon source/sink function of a subtropical, eutrophic lake determined from an overall mass balance and a gas exchange and carbon burial balance

    International Nuclear Information System (INIS)

    Yang Hong; Xing Yangping; Xie Ping; Ni Leyi; Rong Kewen

    2008-01-01

    Although studies on carbon burial in lake sediments have shown that lakes are disproportionately important carbon sinks, many studies on gaseous carbon exchange across the water-air interface have demonstrated that lakes are supersaturated with CO 2 and CH 4 causing a net release of CO 2 and CH 4 to the atmosphere. In order to more accurately estimate the net carbon source/sink function of lake ecosystems, a more comprehensive carbon budget is needed, especially for gaseous carbon exchange across the water-air interface. Using two methods, overall mass balance and gas exchange and carbon burial balance, we assessed the carbon source/sink function of Lake Donghu, a subtropical, eutrophic lake, from April 2003 to March 2004. With the overall mass balance calculations, total carbon input was 14 905 t, total carbon output was 4950 t, and net carbon budget was +9955 t, suggesting that Lake Donghu was a great carbon sink. For the gas exchange and carbon burial balance, gaseous carbon (CO 2 and CH 4 ) emission across the water-air interface totaled 752 t while carbon burial in the lake sediment was 9477 t. The ratio of carbon emission into the atmosphere to carbon burial into the sediment was only 0.08. This low ratio indicates that Lake Donghu is a great carbon sink. Results showed good agreement between the two methods with both showing Lake Donghu to be a great carbon sink. This results from the high primary production of Lake Donghu, substantive allochthonous carbon inputs and intensive anthropogenic activity. Gaseous carbon emission accounted for about 15% of the total carbon output, indicating that the total output would be underestimated without including gaseous carbon exchange. - Due to high primary production, substantive allochthonous carbon inputs and intensive anthropogenic acitivity, subtropical, eutrophic Lake Donghu is a great carbon sink

  8. Integral Ring Carbon-Carbon Piston

    Science.gov (United States)

    Northam, G. Burton (Inventor)

    1999-01-01

    An improved structure for a reciprocating internal combustion engine or compressor piston fabricate from carbon-carbon composite materials is disclosed. An integral ring carbon-carbon composite piston, disclosed herein, reduces the need for piston rings and for small clearances by providing a small flexible, integral component around the piston that allows for variation in clearance due to manufacturing tolerances, distortion due to pressure and thermal loads, and variations in thermal expansion differences between the piston and cylinder liner.

  9. Carbon dioxide sequestration by mineral carbonation

    NARCIS (Netherlands)

    Huijgen, W.J.J.

    2007-01-01

    The increasing atmospheric carbon dioxide (CO2) concentration, mainly caused by fossil fuel combustion, has lead to concerns about global warming. A possible technology that can contribute to the reduction of carbon dioxide emissions is CO2 sequestration by mineral carbonation. The basic concept

  10. Synthesis of carbon nanotubes by catalytic vapor decomposition ...

    Indian Academy of Sciences (India)

    Carbon nanotubes (CNTs); catalytic vapor decomposition; soap bubble mass flowmeter. ... [4,13,14], makes them an excellent candidate for use as a dielectric in supercapac- itors [15]. ... the change in liquid level in the scrubber. After the ...

  11. Acceleration of 14C beams in electrostatic accelerators

    International Nuclear Information System (INIS)

    Rowton, L.J.; Tesmer, J.R.

    1981-01-01

    Operational problems in the production and acceleration of 14 C beams for nuclear structure research in Los Alamos National Laboratory's Van de Graaff accelerators are discussed. Methods for the control of contamination in ion sources, accelerators and personnel are described. Sputter source target fabrication techniques and the relative beam production efficiencies of various types of bound particulate carbon sputter source targets are presented

  12. Synthesis of sup 14 C-radiolabelled Tilmicosin

    Energy Technology Data Exchange (ETDEWEB)

    Crouse, G D; Terando, N H [Lilly (Eli) and Co., Indianapolis, IN (USA). Lilly Research Labs.

    1989-04-01

    Tilmicosin was radiolabelled with carbon-14 on the 3,5-dimethylpiperidinyl sidechain as a requirement for animal metabolism studies. A new radiosynthesis of 3,5-dimethyl-piperidine was developed for this purpose. Incorporation into the desmycosin nucleus was accomplished by a reductive amination reaction. (author).

  13. Chernobyl, 14 years later

    International Nuclear Information System (INIS)

    2000-01-01

    This report draws an account of the consequences of Chernobyl accident 14 years after the disaster. It is made up of 8 chapters whose titles are: 1) Some figures about Chernobyl accident, 2) Chernobyl nuclear power plant, 3)Sanitary consequences of Chernobyl accident, 4) The management of contaminated lands, 5) The impact in France of Chernobyl fallout, 6) International cooperation, 7) More information about Chernobyl and 8) Glossary

  14. 14-plex Feasibility Report

    Energy Technology Data Exchange (ETDEWEB)

    Kotongan, Victoria Hazel [Native Village of Unalakleet

    2013-06-21

    The Native Village of Unalakleet project was a feasibility study for a retrofit of a “tribally owned” three story, 14 apartment complex located in Unalakleet, Alaska. The program objective and overall goal was to create a plan for retrofitting to include current appraised value and comparable costs of new construction to determine genuine feasibility as low-income multi-family housing for tribal members.

  15. Electroanalytical chemistry. Volume 14

    International Nuclear Information System (INIS)

    Bard, A.J.

    1986-01-01

    This volume is part of a series aimed at authoritative reviews of electroanalytical techniques and related areas of investigation. Volume 14 clearly maintains the high standards and proven usefulness of the series. Topics covered include conformation change and isomerization associated with electrode reactions, infrared vibrational spectroscopy of the electrode-solution interface, and precision in linear sweep and cyclic voltametry. A short history of electrochemical techniques which include the term square wave is provided

  16. Composite carbon foam electrode

    Science.gov (United States)

    Mayer, Steven T.; Pekala, Richard W.; Kaschmitter, James L.

    1997-01-01

    Carbon aerogels used as a binder for granularized materials, including other forms of carbon and metal additives, are cast onto carbon or metal fiber substrates to form composite carbon thin film sheets. The thin film sheets are utilized in electrochemical energy storage applications, such as electrochemical double layer capacitors (aerocapacitors), lithium based battery insertion electrodes, fuel cell electrodes, and electrocapacitive deionization electrodes. The composite carbon foam may be formed by prior known processes, but with the solid particles being added during the liquid phase of the process, i.e. prior to gelation. The other forms of carbon may include carbon microspheres, carbon powder, carbon aerogel powder or particles, graphite carbons. Metal and/or carbon fibers may be added for increased conductivity. The choice of materials and fibers will depend on the electrolyte used and the relative trade off of system resistivty and power to system energy.

  17. Synthesis of 14C and 32P double labelled triethylphosphine

    International Nuclear Information System (INIS)

    Kanska, M.; Drabarek, S.

    1979-01-01

    The synthesis of 14 C and 32 P double labelled triethylphosphine has been carried out using red phosphorus [ 32 P] and barium carbonate [ 14 C] as starting materials. The product of the reaction has been separated by gas chromatography. The 32 P radioactivity assay of the obtained product was performed by the liquid scintillation technique. The 14 C radioactivity was determined by the liquid scintillation technique and internal gas counting method. The radioactivity measurements have served to determine the total yield of double labelled triethylphosphine. (author)

  18. Sources of C-14 generation and associated doses; Fuentes de generacion de C-14 y dosis asociadas

    Energy Technology Data Exchange (ETDEWEB)

    Amado, Valeria A; Biaggio, Alfredo L; Canoba, Analia C; Curti, Adriana R. [Autoridad Regulatoria Nuclear, Buenos Aires (Argentina)], E-mail: vamado@cae.arn.gov.ar

    2009-07-01

    C-14 is a radioactive isotope of C with a half-life of 5700 years that decays to N-14 by emission of beta radiation. It is naturally produced in the upper atmosphere by cosmic ray neutrons via the (n;p) reaction over N-14. Anthropogenic C-14 has been generated in the past by atmospheric nuclear weapon tests and it is currently produced during the operation of nuclear reactors. Once released this radionuclide behaves in the biosphere as the standard carbon cycle. Since the beginning of the industrial period the relationship Carbon-14/Stable Carbon has changed continuously, and so the dose incurred by the world population. In this paper the main anthropogenic activities that modified such relationship are presented and analyzed: the Suess effect and the generation of nuclear energy. It is concluded that the current trend of reduction of the total dose due to C-14 will continue during the next decades. Finally it is indicated that in order to prevent an excessive accumulation of this radionuclide in the biosphere, actions should be collectively implemented to be effective. (author) [Spanish] El C-14 es un isotopo radiactivo del C con un periodo de semidesintegracion igual a 5700 anios y que decae a N-14 por emision de radiacion beta. Se produce naturalmente en las altas capas de la atmosfera debido a la reaccion N-14(n,p)C-14 inducida por neutrones lentos de rayos cosmicos. El C-14 antropogenico se genero debido a los ensayos nucleares y actualmente es producido durante la operacion de los reactores nucleares. Una vez liberado se incorpora a la biosfera a traves del ciclo del carbono. A partir de los inicios del periodo industrial la relacion C-14/C-estable, y por ende la dosis debida a C-14 que recibiria la poblacion mundial, ha variado continuamente. El objetivo del presente trabajo es presentar y analizar los distintos factores antropogenicos que modifican la concentracion de C-14, en particular el efecto Suess y la generacion de energia nuclear. Se observa que las

  19. Carbon Nanomembranes

    Science.gov (United States)

    Angelova, Polina; Gölzhäuser, Armin

    2017-03-01

    This chapter describes the formation and properties of one nanometer thick carbon nanomembranes (CNMs), made by electron induced cross-linking of aromatic self-assembled monolayers (SAMs). The cross-linked SAMs are robust enough to be released from the surface and placed on solid support or over holes as free-standing membranes. Annealing at 1000K transforms CNMs into graphene accompanied by a change of mechanical stiffness and electrical resistance. The developed fabrication approach is scalable and provides molecular level control over thickness and homogeneity of the produced CNMs. The mechanisms of electron-induced cross-linking process are discussed in details. A variety of polyaromatic thiols: oligophenyls as well as small and extended condensed polycyclic hydrocarbons have been successfully employed, demonstrating that the structural and functional properties of the resulting nanomembranes are strongly determined by the structure of molecular monolayers. The mechanical properties of CNMs (Young's modulus, tensile strength and prestress) are characterized by bulge testing. The interpretation of the bulge test data relates the Young's modulus to the properties of single molecules and to the structure of the pristine SAMs. The gas transport through the CNM is measured onto polydimethylsiloxane (PDMS) - thin film composite membrane. The established relationship of permeance and molecular size determines the molecular sieving mechanism of permeation through this ultrathin sheet.

  20. Atmospheric carbon reduction by urban trees

    International Nuclear Information System (INIS)

    Nowak, D.J.

    1993-01-01

    Trees, because they sequester atmospheric carbon through their growth process and conserve energy in urban areas, have been suggested as one means to combat increasing levels of atmospheric carbon. Analysis of the urban forest in Oakland, California (21% tree cover), reveals a tree carbon storage level of 11·0 metric tons/hectare. Trees in the area of the 1991 fire in Oakland stored approximately 14,500 metric tons of carbon, 10% of the total amount stored by Oakland's urban forest. National urban forest carbon storage in the United States (28% tree cover) is estimated at between 350 and 750 million metric tons. Establishment of 10 million urban trees annually over the next 10 years is estimated to sequester and offset the production of 363 million metric tons of carbon over the next 50 years-less than 1% of the estimated carbon emissions in the United States over the same time period. Advantages and limitations of managing urban trees to reduce atmospheric carbon are discussed. 36 refs., 2 figs., 3 tabs