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Sample records for atmospheric tritium gas

  1. Atmospheric tritium. Measurement and application

    International Nuclear Information System (INIS)

    Frejaville, Gerard

    1967-02-01

    The possible origins of atmospheric tritium are reviewed and discussed. A description is given of enrichment (electrolysis and thermal diffusion) and counting (gas counters and liquid scintillation counters) processes which can be used for determining atmospheric tritium concentrations. A series of examples illustrates the use of atmospheric tritium for resolving a certain number of hydrological and glaciological problems. (author) [fr

  2. Tritium gas and tritiated water vapour behaviour in the environment from releases into the atmosphere from fusion reactors

    International Nuclear Information System (INIS)

    Velarde, Marta; Perlado, Manuel

    2001-01-01

    The diffusion of tritium from fusion reactors follows different ways according to the present chemical form, tritium gas or tritiated water vapour. The atmospheric conditions, speed and direction of the wind, rain intensity or stability class, are key factors in the dry and wet deposition. The obtained results demonstrate that the wet deposition is critical for the incorporation of the tritiated water vapour to the natural biological chain. However, the dry deposition is the factor that influences in the tritium gas form. The conversion of HT into HTO in the soil is rapid (1-7 days), and 20% of HT deposited in the soil is reemitted to the atmosphere in the form HTO, while the rest incorporates into the biological cycle. The rain factor accelerates the incorporation of tritium to the ground, the superficial waters and the underground waters

  3. Conversion of tritium gas to tritiated water

    International Nuclear Information System (INIS)

    Papagiannakopoulos, P.J.; Easterly, C.E.

    1979-05-01

    The mechanisms of conversion of tritium gas to tritiated water (HTO) have been examined for several tritium gaseous mixtures. The physical and chemical processes involved in the self-radiolysis of such mixtures have been analyzed and the kinetics involved in the formation of HTO has been presented. It has been determined that the formation of the H and/or OH free radicals, as intermediate species, are of significance in the formation of HTO. Therefore, the problem of reducing the rate of formation of tritiated water in a mixture of gaseous tritium with atmospheric components is one of finding an effective scavenger for the H and/or OH free radicals

  4. Development of a code to simulate dispersion of atmospheric released tritium gas in the environmental media and to evaluate doses. TRIDOSE

    International Nuclear Information System (INIS)

    Murata, Mikio; Noguchi, Hiroshi; Yokoyama, Sumi

    2000-11-01

    A computer code (TRIDOSE) was developed to assess the environmental impact of atmospheric released tritium gas (T 2 ) from nuclear fusion related facilities. The TRIDOSE simulates dispersion of T 2 and resultant HTO in the atmosphere, land, plant, water and foods in the environment, and evaluates contamination concentrations in the media and exposure doses. A part of the mathematical models in TRIDOSE were verified by comparison of the calculation with the results of the short range (400 m) dispersion experiment of HT gas performed in Canada postulating a short-time (30 minutes) accidental release. (author)

  5. Development of a code to simulate dispersion of atmospheric released tritium gas in the environmental media and to evaluate doses. TRIDOSE

    Energy Technology Data Exchange (ETDEWEB)

    Murata, Mikio [Nuclear Engineering Co., Ltd., Hitachi, Ibaraki (Japan); Noguchi, Hiroshi; Yokoyama, Sumi [Japan Atomic Energy Research Inst., Tokai, Ibaraki (Japan). Tokai Research Establishment

    2000-11-01

    A computer code (TRIDOSE) was developed to assess the environmental impact of atmospheric released tritium gas (T{sub 2}) from nuclear fusion related facilities. The TRIDOSE simulates dispersion of T{sub 2} and resultant HTO in the atmosphere, land, plant, water and foods in the environment, and evaluates contamination concentrations in the media and exposure doses. A part of the mathematical models in TRIDOSE were verified by comparison of the calculation with the results of the short range (400 m) dispersion experiment of HT gas performed in Canada postulating a short-time (30 minutes) accidental release. (author)

  6. In vitro determination of oxidation of atmospheric tritium gas in vegetation and soil in Ibaraki and Gifu, Japan

    International Nuclear Information System (INIS)

    Ichimasa, Michiko; Ichimasa, Yusuke; Suzuki, Masatomo; Obayashi, Haruo; Sakuma, Youichi

    1999-01-01

    To quantify the rate of oxidation of tritium gas (referred to as HT) to tritiated water in the environment, various woody and herbaceous plant leaves and roots, mosses and lichens taken from a forest and fields in Ibaraki prefecture, and a forest in Toki, Gifu prefecture, were investigated as to their ability to oxidize atmospheric HT in vitro experiments. The HT oxidation activity in vegetation was compared with that in the surrounding surface soil (0-5 cm in depth). The rate of oxidation of HT in woody plant leaves including pine needles was extremely low, only about 1/10000-1/1000 that in the surface soil, as well as in herbaceous plant leaves with some exceptions (Phalaris arundinacea and Vaccinium smallii), whereas the rate in mosses and lichens was 50-500 times that in pine needles. The HT oxidation activity in roots of several plants including Phalaris arundinacea, Pieris japonica and Lespedeza homoloba was quite high and comparable to that in the surrounding surface soil. These results suggest that mosses, lichens and the leaves or roots of particular plants with high HT oxidation activity can be used to monitor the accidental release of HT into the environment. (author)

  7. Atmospheric tritium 1968-1984. Tritium Laboratory data report No. 14

    International Nuclear Information System (INIS)

    Oestlund, H.G.; Mason, A.S.

    1985-04-01

    Tritium in the form of water, HTO, from the atmospheric testing of nuclear devices in the 60s has now mainly disappeared from the atmosphere and entered the ocean. The additions of such tritium from Chinese and French tests in the 70s were observed but did not make a big impression on the diminishing inventory of atmospheric HTO. Tritium in elemental form, HT, went through a maximum in the mid 70s, apparently primarily as a results of some underground testing of large nuclear devices and releases from civilian and military nuclear industry. The mid 70s maximum was 1.3 kg of tritium in this form, and in 1984 0.5 kg remain. The disappearance is slower than the decay rate of tritium, so sources must still have been present during this time. The global distribution shows, not unexpectedly, smaller inventory in the Southern Hemisphere across the equator and thus southward transport of HT. The chemical lifetime of hydrogen gas in the atmosphere, assuming the elemental tritium being in the form of HT, not T 2 , has been estimated between 6 and 10 years. It is to be expected that increasing activity of nuclear fuel reprocessing would in the near future again increase the global tritium gas inventory. Tritium in the form of light hydrocarbons, primarily methane, has also been measured, and in this form a quantity of 200 g of tritium resided in the global atmosphere 1956 to 1976. By 1982 it had decreased to 50 g. 25 refs., 5 figs., 11 tabs

  8. Uptake of atmospheric tritium by market foods

    International Nuclear Information System (INIS)

    Inoue, Y.; Tanaka-Miyamoto, K.; Iwakura, T.

    1992-01-01

    In this paper uptake of tritium by market foods from tritiated water vapor in the air is investigated using cereals and beans purchased in Deep River, Canada. The concentrations of tissue free water tritium (TFWT) and organically bound tritium (OBT) range from 12 to 79% and from 10 to 38% respectively, of that estimated for atmospheric water vapor of the sampling month. The specific activity ratios of OBT to TFWT were constant for cereals, but variable for beans. The elevated OBT was shown to be the result of isotopic exchange of labile hydrogen by the fact that washing the foods with tritium free-water reduced their tritium contents to levels characteristic of their production sites

  9. EFFECTS OF TRITIUM GAS EXPOSURE ON EPDM ELASTOMER

    Energy Technology Data Exchange (ETDEWEB)

    Clark, E.

    2009-12-11

    Samples of four formulations of ethylene-propylene diene monomer (EPDM) elastomer were exposed to initially pure tritium gas at one atmosphere and ambient temperature for various times up to about 420 days in closed containers. Two formulations were carbon-black-filled commercial formulations, and two were the equivalent formulations without filler synthesized for this work. Tritium effects on the samples were characterized by measuring the sample volume, mass, flexibility, and dynamic mechanical properties and by noting changes in appearance. The glass transition temperature was determined by analysis of the dynamic mechanical properties. The glass transition temperature increased significantly with tritium exposure, and the unfilled formulations ceased to behave as elastomers after the longest tritium exposure. The filled formulations were more resistant to tritium exposure. Tritium exposure made all samples significantly stiffer and therefore much less able to form a reliable seal when employed as O-rings. No consistent change of volume or density was observed; there was a systematic lowering of sample mass with tritium exposure. In addition, the significant radiolytic production of gas, mainly protium (H{sub 2}) and HT, by the samples when exposed to tritium was characterized by measuring total pressure in the container at the end of each exposure and by mass spectroscopy of a gas sample at the end of each exposure. The total pressure in the containers more than doubled after {approx}420 days tritium exposure.

  10. Development of compact tritium confinement system using gas separation membrane

    International Nuclear Information System (INIS)

    Hayashi, Takumi; Okuno, Kenji

    1994-01-01

    In order to develop more compact and cost-effective tritium confinement system for fusion reactor, a new system using gas separation membranes has been studied at the Tritium Process Laboratory in the Japan Atomic Energy Research Institute. The preliminary result showed that the gas separation membrane system could reduce processing volume of tritium contaminated gas to more than one order of magnitude compared with the conventional system, and that most of tritiated water vapor (humidity) could be directly recovered by water condenser before passing through dryer such as molecular sieves. More detail investigations of gas separation characteristics of membrane were started to design ITER Atmospheric Detritiation System (ADS). Furthermore, a scaled polyimide membrane module (hollow-filament type) loop was just installed to investigate the actual tritium confinement performance under various ITER-ADS conditions. (author)

  11. A novel atmospheric tritium sampling system

    Science.gov (United States)

    Qin, Lailai; Xia, Zhenghai; Gu, Shaozhong; Zhang, Dongxun; Bao, Guangliang; Han, Xingbo; Ma, Yuhua; Deng, Ke; Liu, Jiayu; Zhang, Qin; Ma, Zhaowei; Yang, Guo; Liu, Wei; Liu, Guimin

    2018-06-01

    The health hazard of tritium is related to its chemical form. Sampling different chemical forms of tritium simultaneously becomes significant. Here a novel atmospheric tritium sampling system (TS-212) was developed to collect the tritiated water (HTO), tritiated hydrogen (HT) and tritiated methane (CH3T) simultaneously. It consisted of an air inlet system, three parallel connected sampling channels, a hydrogen supply module, a methane supply module and a remote control system. It worked at air flow rate of 1 L/min to 5 L/min, with temperature of catalyst furnace at 200 °C for HT sampling and 400 °C for CH3T sampling. Conversion rates of both HT and CH3T to HTO were larger than 99%. The collecting efficiency of the two-stage trap sets for HTO was larger than 96% in 12 h working-time without being blocked. Therefore, the collected efficiencies of TS-212 are larger than 95% for tritium with different chemical forms in environment. Besides, the remote control system made sampling more intelligent, reducing the operator's work intensity. Based on the performance parameters described above, the TS-212 can be used to sample atmospheric tritium in different chemical forms.

  12. Conversion of tritium gas to tritiated water in the environment

    International Nuclear Information System (INIS)

    Noguchi, Hiroshi; Kato, Shohei

    1985-01-01

    The literature on conversion of tritium gas to tritiated water in various environments is reviewed. The conversion mechanisms and the conversion rates are as follows. 1. In the oxidation with oxygen and the isotopic exchange with water, tritium β-rays and metal catalyst are effective. The oxidation rate is ∼ 0.02 %/day at initial tritium concentration ≤ 10 -2 Ci/l and ∼ 2 %/day at 1 Ci/l. In the presence of oxygen and water, it is not clear whether the exchange reaction occurs or not because of the small amount of data. 2. For biological conversion, soil microorganisms contribute significantly. The conversion rate is greater than 10 %/hr. The tritium gas deposition velocity, which includes the uptake rate of tritium gas by soil and the conversion rate, ranges from 0.0025 to 0.11 cm/sec and is influenced by temperature and moisture of the soil. 3. Tritium gas is converted to the tritiated water through the reaction with hydroxyl radical produced by sunlight in the atmosphere. (author)

  13. A Gas Target with a Tritium Gas Handling System

    Energy Technology Data Exchange (ETDEWEB)

    Holmqvist, B; Wiedling, T

    1963-12-15

    A detailed description is given of a simple tritium gas target and its tritium gas filling system, and how to put it into operation. By using the T (p,n) He reaction the gas target has been employed for production of monoenergetic fast neutrons of well defined energy and high intensity. The target has been operated successfully for a long time.

  14. Atmospheric tritium. Progress report, July 1, 1975--March 31, 1976

    International Nuclear Information System (INIS)

    Oestlund, H.G.; Mason, A.S.

    1976-01-01

    Progress is reported in the development of field equipment for sampling tritium in environmental samples. The performance of prototype tritiated hydrocarbon samples is discussed. Data are presented on the content of tritium in samples of rain water collected in Miami, Florida, Western Samoa, and Barbados during 1975, and tritium compounds in atmospheric samples collected at various world locations during 1975

  15. Survey of pumps for tritium gas

    International Nuclear Information System (INIS)

    Dowell, T.M.

    1983-05-01

    This report considers many different types of pumps for their possible use in pumping tritium gas in the low, intermediate and high vacuum ranges. No one type of pump is suitable for use over the wide range of pumping pressure required in a typical pumping system. The favoured components for such a system are: bellows pump (low vacuum); orbiting scroll pump (intermediate vacuum); magnetically suspended turbomolecular pump (high vacuum); cryopump (high vacuum). Other pumps which should be considered for possible future development are: mound modified vane pump; SRTI wobble pump; roots pump with canned motor. It is proposed that a study be made of a future tritium pumping system in a Canadian tritium facility, e.g. a tritium laboratory

  16. Tritium recovery and separation from CTR plasma exhausts and secondary containment atmospheres

    International Nuclear Information System (INIS)

    Forrester, R.C. III; Watson, J.S.

    1975-01-01

    Recent experimental successes have generated increased interest in the development of thermonuclear reactors as power sources for the future. This paper examines tritium containment problems posed by an operating CTR and sets forth some processing schemes currently being evaluated at the Oak Ridge National Laboratory. An appreciation of the CTR tritium management problem can best be realized by recalling that tritium production rates for various fission reactors range from 2 x 10 4 to 9 x 10 5 Ci/yr per 1000 MW(e). Present estimates of tritium production in a CTR blanket exceed 10 9 Ci/yr for the same level of power generation, and tritium process systems may handle 10 to 20 times that amount. Tritium's high permeability through most materials of construction at high temperatures makes secondary containment mandatory for most piping. Processing of these containment atmospheres will probably involve conversion of the tritium to a nonpermeating form (T 2 O) followed by trapping on conventional beds of desiccant material. In a similar fashion, all purge streams and process fluid vent gases will be subjected to tritium recovery prior to atmospheric release. Two tritium process systems will be required, one to recover tritium produced by breeding in the blanket and another to recover unburned tritium in the plasma exhaust. Plasma exhaust processing will be unconventional since the exhaust gas pressure will lie between 10 -3 and 10 -6 torr. Treatment of this gas stream will entail the removal of small quantities of protium and helium from a much larger deuterium-tritium mixture which will be recycled. (U.S.)

  17. Analysis on tritium permeation in tritium storage bed with gas flowing calorimetry

    Energy Technology Data Exchange (ETDEWEB)

    Nakamura, Hirofumi; Hayashi, Takumi; Suzuki, Takumi; Nishi, Masataka [Japan Atomic Energy Research Inst., Naka Fusion Research Establishment, Department of Fusion Engineering Research, Naka, Ibaraki (Japan); Yoshida, Hiroshi [Japan Atomic Energy Research Inst., Naka Fusion Research Establishment, ITER-Joint Centeral Team, Naka, Ibaraki (Japan)

    2000-10-01

    Tritium permeation amount in a tritium storage bed with gas flowing calorimetric was evaluated under a condition of new operation mode for International Thermonuclear Experimental Reactor (ITER). As a result, tritium permeation under the new operation mode was estimated to be about twice of that under the practical operation mode. This result show that it would be regardless in a view point of material control of tritium, however, it was suggested to be required additional tritium removal or evacuate system in a view points of safety control or performance of accountability or thermal insulating of the tritium storage bed. (author)

  18. Gas chromatography at the Tritium Laboratory Karlsruhe

    International Nuclear Information System (INIS)

    Laesser, R.; Gruenhagen, S.

    2003-08-01

    Among the analytical techniques (mass spectrometry, laser Raman spectroscopy, gas chromatography, use of ionisation chambers) employed at the Tritium Laboratory Karlsruhe (TLK), gas chromatography plays a prominent role. The main reasons for that are the simplicity of the gas chromatographic separation process, the small space required for the equipment, the low investment costs in comparison to other methods, the robustness of the equipment, the simple and straightforward analysis and the fact that all gas species of interest (with the exception of water) can easily be detected by gas chromatographic means. The conventional gas chromatographs GC1 and GC2 used in the Tritium Measurement Techniques (TMT) System of the TLK and the gas chromatograph GC3 of the experiment CAPER are presented in detail, by discussing their flow diagrams, their major components, the chromatograms measured by means of various detectors, shortcomings and possible improvements. One of the main disadvantages of the conventional gas chromatography is the long retention times required for the analysis of hydrogen gas mixtures. To overcome this disadvantage, micro gas chromatography for hydrogen analysis was developed. Reduction of the retention times by one order of magnitude was achieved. (orig.)

  19. Use of passive sampling for atmospheric tritium monitoring

    Energy Technology Data Exchange (ETDEWEB)

    Caldeira Ideias, P.; Pierrard, O.; Tournieux, D. [Institut de Radioprotection et de Surete Nucleaire - IRSN (France); Tenailleau, L. [Marine nationale (France)

    2014-07-01

    Tritium is one of the most important radionuclide in environmental radiological monitoring. In French civil and military nuclear facilities, the releases levels are between 100 to 100 000 higher than any other radionuclide (rare gas excluded). Moreover these levels will probably increase in the next decades. With an average energy of 6 keV, the beta particle from tritium radioactive decay is difficult to detect and quantify within the environmental levels. To monitor the tritium in the air, French actors (authorities, operator, and experts) commonly use atmospheric bubblers and water vapour condensers. This type of sampling approach is time-consuming and very costly. To simplify and complete these methods, the Institute for Radiological Protection and Nuclear Safety (IRSN), had developed an atmospheric tritium monitoring device based on passive sampling. The passive sampler developed consists in a small container designed with a patented specific geometry and filled with 13X molecular sieve. This system is based on free diffusion flow principle (Fick's law). The driving force is the partial pressure gradient existing between the environmental atmosphere and the passive sampler. The constancy of the sampling rate for different moisture conditions assures the representativeness of the proposed device. The desorption bench developed specifically allows the recovery of 99% of the water vapour sampled in the molecular sieve. More than 99% of the sampled tritium (HTO) activity is recovered in the range between 0 and 100 Bq.L{sup -1}. Above 100 Bq.L{sup -1} to 25 k Bq.L{sup -1} (max tested activity), it was verified that no more than 3% of the tritium remains in the molecular sieve.. Thus, the use of passive sampler provides: - a representative sampling method, - a good detection limit (0,01 Bq.m{sup -3}), - no electric power supply needs, - a wide range of sampling duration (1 day to 1 month), - a low-cost method for monitoring. Different performance tests were

  20. Analysis of tritium releases to the atmosphere by a CTR

    International Nuclear Information System (INIS)

    Renne, D.S.; Sandusky, W.F.; Dana, M.T.

    1975-08-01

    Removal by atmospheric processes of routinely and accidentally released tritium from a controlled thermonuclear reactor (CTR) was investigated. Based on previous studies, the assumed form of the tritium for this analysis was HTO or tritiated water vapor. Assuming a CTR operation in Morris, Illinois, surface water and ground-level air concentration values of tritium were computed for three space (or time) scales: local (50 Km of a plant), regional (up to 1000 Km of the plant), and global

  1. Dose Assessment Model for Chronic Atmospheric Releases of Tritium

    International Nuclear Information System (INIS)

    Shen Huifang; Yao Rentai

    2010-01-01

    An improved dose assessment model for chronic atmospheric releases of tritium was proposed. The proposed model explicitly considered two chemical forms of tritium.It was based on conservative assumption of transfer of tritiated water (HTO) from air to concentration of HTO and organic beam tritium (OBT) in vegetable and animal products.The concentration of tritium in plant products was calculated based on considering dividedly leafy plant and not leafy plant, meanwhile the concentration contribution of tritium in the different plants from the tritium in soil was taken into account.Calculating the concentration of HTO in animal products, average water fraction of animal products and the average weighted tritium concentration of ingested water based on the fraction of water supplied by each source were considered,including skin absorption, inhalation, drinking water and food.Calculating the annual doses, the ingestion doses were considered, at the same time the contribution of inhalation and skin absorption to the dose was considered. Concentrations in foodstuffs and dose of annual adult calculated with the specific activity model, NEWTRI model and the model proposed by the paper were compared. The results indicate that the model proposed by the paper can predict accurately tritium doses through the food chain from chronic atmospheric releases. (authors)

  2. Organically bound tritium (OBT) for various plants in the vicinity of a continuous atmospheric tritium release

    International Nuclear Information System (INIS)

    Vichot, L.; Boyer, C.; Boissieux, T.; Losset, Y.; Pierrat, D.

    2008-01-01

    In order to quantify tritium impact on the environmental, we studied vegetation continuously exposed to a tritiated atmosphere. We chose lichens as bio-indicators, trees for determination of past tritium releases of the Valduc Centre, and lettuce as edible vegetables for dose calculation regarding neighbourhood. The Pasquill and Doury models from the literature were tested to estimate tritium concentration in the air around vegetable for distance from the release point less than 500 m. The results in tree rings show that organically bound tritium (OBT) concentration was strongly correlated with tritium releases. Using the GASCON model, the modelled variation of OBT concentration with distance was correlated with the measurements. Although lichens are recognized as bio-indicators, our experiments show that they were not convenient for environmental surveys because their age is not definitive. Thus, tritium integration time cannot be precisely determined. Furthermore, their biological metabolism is not well known and tritium concentration appears to be largely dependent on species. An average conversion rate of HTO to OBT was determined for lettuce of about 0.20-0.24% h -1 . Nevertheless, even if it is equivalent to values already published in the literature for other vegetation, we have shown that this conversion rate, established by weekly samples, varies by a factor of 10 during the different stages of lettuce development, and that its variation is linked to the biomass derivative

  3. Organically bound tritium (OBT) for various plants in the vicinity of a continuous atmospheric tritium release

    Energy Technology Data Exchange (ETDEWEB)

    Vichot, L. [Commissariat a l' Energie Atomique, CVA/DSTA/SPR/LMSE, 21120 Is-sur-Tille (France)], E-mail: laurent.vichot@cea.fr; Boyer, C.; Boissieux, T.; Losset, Y.; Pierrat, D. [Commissariat a l' Energie Atomique, CVA/DSTA/SPR/LMSE, 21120 Is-sur-Tille (France)

    2008-10-15

    In order to quantify tritium impact on the environmental, we studied vegetation continuously exposed to a tritiated atmosphere. We chose lichens as bio-indicators, trees for determination of past tritium releases of the Valduc Centre, and lettuce as edible vegetables for dose calculation regarding neighbourhood. The Pasquill and Doury models from the literature were tested to estimate tritium concentration in the air around vegetable for distance from the release point less than 500 m. The results in tree rings show that organically bound tritium (OBT) concentration was strongly correlated with tritium releases. Using the GASCON model, the modelled variation of OBT concentration with distance was correlated with the measurements. Although lichens are recognized as bio-indicators, our experiments show that they were not convenient for environmental surveys because their age is not definitive. Thus, tritium integration time cannot be precisely determined. Furthermore, their biological metabolism is not well known and tritium concentration appears to be largely dependent on species. An average conversion rate of HTO to OBT was determined for lettuce of about 0.20-0.24% h{sup -1}. Nevertheless, even if it is equivalent to values already published in the literature for other vegetation, we have shown that this conversion rate, established by weekly samples, varies by a factor of 10 during the different stages of lettuce development, and that its variation is linked to the biomass derivative.

  4. Organically bound tritium (OBT) for various plants in the vicinity of a continuous atmospheric tritium release.

    Science.gov (United States)

    Vichot, L; Boyer, C; Boissieux, T; Losset, Y; Pierrat, D

    2008-10-01

    In order to quantify tritium impact on the environmental, we studied vegetation continuously exposed to a tritiated atmosphere. We chose lichens as bio-indicators, trees for determination of past tritium releases of the Valduc Centre, and lettuce as edible vegetables for dose calculation regarding neighbourhood. The Pasquill and Doury models from the literature were tested to estimate tritium concentration in the air around vegetable for distance from the release point less than 500 m. The results in tree rings show that organically bound tritium (OBT) concentration was strongly correlated with tritium releases. Using the GASCON model, the modelled variation of OBT concentration with distance was correlated with the measurements. Although lichens are recognized as bio-indicators, our experiments show that they were not convenient for environmental surveys because their age is not definitive. Thus, tritium integration time cannot be precisely determined. Furthermore, their biological metabolism is not well known and tritium concentration appears to be largely dependent on species. An average conversion rate of HTO to OBT was determined for lettuce of about 0.20-0.24% h(-1). Nevertheless, even if it is equivalent to values already published in the literature for other vegetation, we have shown that this conversion rate, established by weekly samples, varies by a factor of 10 during the different stages of lettuce development, and that its variation is linked to the biomass derivative.

  5. Removal of tritium from gas-cooled nuclear reactors

    International Nuclear Information System (INIS)

    Nieder, R.

    1976-01-01

    Tritium contained in the coolant gas in the primary circuit of a gas cooled nuclear reactor together with further tritium adsorbed on the graphite used as a moderator for the reactor is removed by introducing hydrogen or a hydrogen-containing compound, for example methane or ammonia, into the coolant gas. The addition of the hydrogen or hydrogen-containing compound to the coolant gas causes the adsorbed tritium to be released into the coolant gas and the tritium is then removed from the coolant gas by passing the mixture of coolant gas and hydrogen or hydrogen-containing compound through a gas purification plant before recirculating the coolant gas through the reactor. 14 claims, 1 drawing figure

  6. Necessity for quality assurance tests of tritium gas

    International Nuclear Information System (INIS)

    Bender, L.; Bhat, R.; Guadagno, J.; Sotomayor, R.; Funkhouser, M.; Plasket, E.

    1989-01-01

    For the past 20 years, the U.S. Army has used self-illuminating tritium excited phosphor vials inside the Lensatic compass for night illumination. Tritium was selected as the illuminating mechanism based on calculations from its half-life that projected its field life to be 12 years. Studies conducted by the Radiation Research Group detected deficiencies between the actual luminosity life of the compass and the projected life. Based on this observation, the group conducted subsequent studies to determine if the discrepancy could be attributed to the phosphor or the composition of the tritium contained in the vial. These studies revealed that the composition of tritium gas used in the compass did not match the specifications set for the gas. The group has since incorporated rigorous quality controls in the specifications to avoid future discrepancies. This work has pointed out the need for all tritium vial users to establish specifications and quality control tests for tritium vials

  7. Performances of an atmospheric tritium sampler and its application

    International Nuclear Information System (INIS)

    Inoue, Yoshikazu; Kahn, B.; Carter, M.W.

    1983-01-01

    A sampling system for atmospheric tritium in the form of water vapor, hydrogen and hydrocarbons was designed and built. The air was passed first through molecular sieve which adsorbed water vapor, then over palladium catalyst which oxidized hydrogen and adsorbed resulting water in situ, and finally over hot Hopcalite catalyst, which oxidized hydrocarbons and the resulting water was adsorbed on a following molecular sieve column. Three water samples were extracted from adsorbers and their tritium contents were measured by liquid scintillation counting. Performances of this sampler were examined for retrieval of tritiated water from molecular sieve, oxidation of hydrogen on palladium catalyst and oxidation of methane on Hopcalite. The portable sampler was applied to analyze tritium in a duct air of a heavy water moderated research reactor. More than 99% of total tritium was in vapor form. Trace amounts of tritiated hydrogen and hydrocarbon were also detected. This tritium sampler is applicable to detect all of atmospheric tritium as high as ten times of ambient levels. (author)

  8. Tritium release reduction and radiolysis gas formation

    Energy Technology Data Exchange (ETDEWEB)

    Batifol, G.; Douche, Ch.; Sejournant, Ch. [CEA Valduc, 21 - Is-sur-Tille (France)

    2008-07-15

    At CEA Valduc, the usual tritiated waste container is the steel drum. It allows good release reduction performance for middle activity waste but in some cases tritium outgassing from the waste drums is too high. It was decided to over-package each drum in a tighter container called the over-drum. According to good safety practices it was also decided to measure gas composition evolution into the over-drum in order to defect hydrogen formation over time. After a few months, a significant release reduction was observed. Additionally there followed contamination reduction in the roof storage building rainwater. However hydrogen was also observed in some over-drums, in addition to other radiolysis products. Catalyst will be added to manage the hydrogen risk in the over-drums. (authors)

  9. Tritium uptake in cultivated plants after short-term exposure to atmospheric tritium

    International Nuclear Information System (INIS)

    Diabate, S.; Strack, S.; Paunescu, N.

    1998-01-01

    The tritium behavior in crop plants is of particular interest for the prediction of doses to humans due to ingestion. Tritium is present in plants in two forms: tritium free water tissue (TWT) and organically bound tritium (OBT). The both forms are to be considered in models calculating the ingestion dose. Potato plants belong to the major food crops in many countries and were chosen as representatives of crops whose edible parts grow under ground. Green bean were chosen as representatives of vegetables relevant in human diet. This vegetable may be consumed as green pod and it may be conserved over a long period of time. Green bean and potato plants were exposed to tritiated water vapor in the atmosphere during their generative phase of development. The uptake of tritium and the conversion into organic matter was studied under laboratory conditions at two different light intensities. The tritium concentrations in plants were followed until harvest. In leaves, the tritium uptake into tissue water under night conditions was 5-6 times lower than under day-time conditions. The initial incorporation into organic matter under night conditions was 0.7% of the tissue water concentration in leaves of both plant species. However, under light irradiation, this value increased to only 1.8% in bean leaves and 0.9% in potato leaves, which indicates a participation of processes other than photosynthesis in tritium incorporation into organic material. Organically bound tritium (OBT) was translocated into pods and tubers which represented a high percentage of the total organically bound tritium at harvest. The behavior of total OBT in all plants under study showed that OBT, once generated, is lost very slowly until harvest, in particular when storage organs of plants were in their phase of development at the time of exposure. OBT is translocated into the storage organs which may be used in the human diet and thus may contribute to the ingestion dose for a long time after the

  10. Studies on tritium incorporation into wheat plants after short-term exposure to atmospheric tritium

    International Nuclear Information System (INIS)

    Diabate, S.; Strack, S.; Raskob, W.

    1996-01-01

    The paper summarizes the results of a series of laboratory experiments to study the uptake, loss, conversion and translocation of tritium in wheat plants following a short-term exposure to atmospheric tritiated water vapour (HTO) under laboratory conditions. The experiments were accompanied by the development of a Plant-OBT-Model to calculate the tritium behaviour in wheat. Exposures of potted plants were carried out between anthesis and maturity, under day conditions at two different light intensities (900 μmol m -2 s -1 and 120 μmol m -2 s -1 photosynthetic active radiation) and under night conditions. In leaves, the tritium uptake into tissue water tritium (TWT) was about four times lower under night conditions than day conditions. Organically bound tritium (OBT) was generated in leaves, stems and ears under day as well as under night conditions. The initial relative OBT concentrations in leaves observed under night conditions were about 50% of those under day conditions. OBT was translocated into the grain in dependence on the growth rate of the grain. Due to incorporation of new organic matter with lower OBT concentration into the grain, the specific OBT concentrations decreased slightly until harvest but the total OBT was rather constant. Once translocation to grain has taken place, OBT is lost only slowly. The growth of the plants has been calibrated with the measured growth data of winter wheat and spring wheat. Subsequently, the tritium incorporation was calibrated using the results of the exposure experiments in the same year. The final OBT concentration in the grain can be predicted with sufficient precision. However, the modelling of the OBT formation and turnover processes right after exposure to tritium needs improvement. A comprehensive validation of the model with independent data sets is still necessary. (J.P.N.)

  11. Tritium inventory measurements by 'in-bed' gas flowing calorimetry

    International Nuclear Information System (INIS)

    Hayashi, T.; Suzuki, T.; Yamada, M.; Okuno, K.

    1996-01-01

    In order to establish the 'in-bed' tritium accounting technology for the ITER scale tritium storage system, a gas flowing calorimetry has been studied using a scaled ZrCo bed (25 g tritium capacity). The basic calorimetric characteristics, steady state temperature raise of He gas stream flowing through a secondary coil line fixed in the ZrCo tritide, was measured and correlated with the stored tritium inventory. The results shows that about 4 degrees raise of He stream temperature can be detected for each gram of tritium storage. The sensitivity of this calorimetry is about 0.05 g of tritium, calculated by 0.2 degrees of temperature sensor error. The accuracy is better than 0.25 g of tritium on 25 g storage, evaluated by 2 times of standard deviation from the repeat measurements. This accuracy of < 1% on full storage capacity is satisfied the target accountability to measure ± 1 gram of tritium on 100 g storage for ITER. 13 refs., 7 figs

  12. Tritium release from advanced beryllium materials after loading by tritium/hydrogen gas mixture

    Energy Technology Data Exchange (ETDEWEB)

    Chakin, Vladimir, E-mail: vladimir.chakin@kit.edu [Karlsruhe Institute of Technology, Institute for Applied Materials, Hermann-von-Helmholtz-Platz 1, 76344 Eggenstein-Leopoldshafen (Germany); Rolli, Rolf; Moeslang, Anton; Kurinskiy, Petr; Vladimirov, Pavel [Karlsruhe Institute of Technology, Institute for Applied Materials, Hermann-von-Helmholtz-Platz 1, 76344 Eggenstein-Leopoldshafen (Germany); Dorn, Christopher [Materion Beryllium & Composites, 6070 Parkland Boulevard, Mayfield Heights, OH 44124-4191 (United States); Kupriyanov, Igor [Bochvar Russian Scientific Research Institute of Inorganic Materials, Rogova str., 5, 123098 Moscow (Russian Federation)

    2016-06-15

    Highlights: • A major tritium release peak for beryllium samples occurs at temperatures higher than 1250 K. • A beryllium grade with comparatively smaller grain size has a comparatively higher tritium release compared to the grade with larger grain size. • The pebbles of irregular shape with the grain size of 10–30 μm produced by the crushing method demonstrate the highest tritium release rate. - Abstract: Comparison of different beryllium samples on tritium release and retention properties after high-temperature loading by tritium/hydrogen gas mixture and following temperature-programmed desorption (TPD) tests has been performed. The I-220-H grade produced by hot isostatic pressing (HIP) having the smallest grain size, the pebbles of irregular shape with the smallest grain size (10–30 μm) produced by the crushing method (CM), and the pebbles with 1 mm diameter produced by the fluoride reduction method (FRM) having a highly developed inherent porosity show the highest release rate. Grain size and porosity are considered as key structural parameters for comparison and ranking of different beryllium materials on tritium release and retention properties.

  13. Ionization chamber for measurements of high-level tritium gas

    International Nuclear Information System (INIS)

    Carstens, D.H.W.; David, W.R.

    1980-01-01

    The construction and calibration of a simple ionization-chamber apparatus for measurement of high level tritium gas is described. The apparatus uses an easily constructed but rugged chamber containing the unknown gas and an inexpensive digital multimeter for measuring the ion current. The equipment after calibration is suitable for measuring 0.01 to 100% tritium gas in hydrogen-helium mixes with an accuracy of a few percent. At both the high and low limits of measurements deviations from the predicted theoretical current are observed. These are briefly discussed

  14. Device for measuring the tritium concentration in a measuring gas

    International Nuclear Information System (INIS)

    Koran, P.

    1987-01-01

    The measuring gas is brought into contact via a measuring gas path with a diaphragm permeable to water, which separates the measuring gas path from a counter gas path leading to a proportional detector. The measuring gas path and the counter gas path are in counterflow in the area of diaphragm. The preferably hose diaphragm consists of a well-known ion exchange material, which can be used for gas drying purposes, which is permeable to water and tritium compounds similar to water, but is impermeable to other gases and liquids contained in air, particularly rare gases. In this way, the tritium concentration can be measured with great rare gas suppression. (orig./HP) [de

  15. The Use of natural fatty acids in processing tritium gas

    International Nuclear Information System (INIS)

    El-Sharnouby, A.K.; Abdelgeleel, M.; Eskander, S.B.

    1997-01-01

    Natural unsaturated fatty acid (e.g cotton, corn, litmus, castor and palm oils) were used to fix tritium gas. The data obtained show that the affinity of the different used natural oils fixation of hydrogen (tritium) was in the following order: cotton oils> corn oil> litmus oil> castor oil> palm oil. The quantity of hydrogen (tritium) which can be fixed by one gram cotton oil is about 5.824 ml H 2 (5.56 x 10 1 1 Bq tritium) while one gram corn oil can fix only 5.04 ml H 2 (4.811 x 10 1 1 Bq tritium). Tritiated cotton oil and corn oil can be solidified using an epoxy resin (Araldite-B-W-1193), the polymer sample can contain up to 5% by weight from hydrogenated (tritiated) oils. The results obtained show that the compressive strength measurements of the final solid waste forms (fatty acid/epoxy) increased with increasing curing time and decreased with increasing fatty acid content. The leachability of tritium from the final solid waste forms increased with increasing fatty acid content in the polymer matrix. The cumulative leach fraction of tritium varied between 4.00 x 10 -3 cm and 6.60 x 10 -3 cm according to the experimental conditions. 15 figs., 1 tab

  16. Tritium concentration reducing method in atmosphere in nuclear reactor containment facility

    International Nuclear Information System (INIS)

    Hirasawa, Yoshiya; Kigoshi, Yasutane; Yonenaga, Haruo.

    1992-01-01

    A portion of water content in an atmosphere is condensed by a condensation/evaporation device disposed in a nuclear reactor containment building and then a portion of the condensed water is evaporated in the atmosphere. A portion of hydrogen nuclides constituting the evaporated water content is subjected to isotopic exchange with tritium nuclides in the atmosphere. A portion of water content in the atmosphere applied with the isotopic exchange is condensed in the condensation/evaporation device. That is, the hydrogen nuclides in steams are applied with isotopic exchange with tritium nuclides, and steams incorporating tritium nuclides are condensed again in the condensation/evaporation device, to transfer the tritium nuclides in the atmosphere to condensed water. The condensed water is recovered without releasing the tritium nuclides to the outside of the reactor containment building, thereby enabling to reduce the tritium concentration in the atmosphere. (N.H.)

  17. Environmental effects of a tritium gas release from the Savannah River Plant on December 31, 1975

    International Nuclear Information System (INIS)

    Jacobsen, W.R.

    1976-03-01

    At 10:00 p.m. EST on December 31, 1975, 182,000 Ci of tritium gas was released within about 1.5 min from a tritium processing facility at the Savannah River Plant. The release was caused by the failure of a vacuum gage and was exhausted to the atmosphere by way of a 200-ft-high stack. Winds averaging 20 mph carried the tritium offplant toward the east. Calculations indicate that the puff passed out to sea about 35 miles north of Charleston, South Carolina, about 7 hr after the release occurred. Samples from the facility exhaust system indicated that 99.4 percent of the tritium was in elemental form and 0.6 percent was in the more biologically active oxide (water) form. The maximum potential dose to a person (from inhalation and skin absorption) at the puff centerline on the plant boundary was calculated to be 0.014 mrem, or about 0.01 percent of the annual dose received from natural radioactivity. The integrated dose to the population under the release path was calculated to be 0.2 man-rem before the tritium passed out to sea. Over 300 environmental samples were collected and analyzed following the release. These samples included air moisture, atmospheric hydrogen, vegetation, soil, surface water, milk, and human urine. Positive results were obtained in some onplant and plant perimeter samples; these results aided in confirming the close-in puff trajectory. Tritium concentrations in nearly all samples taken beyond the plant perimeter fell within normal ranges; no urine samples indicated any tritium uptakes as a result of the release. Two milk samples did indicate a measurable tritium uptake; the maximum potential dose to an individual drinking this milk was calculated to be about 0.1 mrem. Because calculated doses from assumed exposure to the tritium are low and analyses of environmental samples indicated no significant accumulation of tritium, it is concluded that no significant environmental effects resulted from the December 31, 1975, tritium release

  18. Atmospheric tritium concentration in the different chemical forms

    International Nuclear Information System (INIS)

    Akata, Naofumi; Kakiuchi, Hideki; Hisamatsu, Shun'ichi; Shima, Nagayoshi

    2012-01-01

    This study aimed at obtaining background tritium concentrations in air at Rokkasho where the first commercial spent nuclear fuel reprocessing plant in Japan has been under construction. Atmospheric tritium was operationally separated into HTO, HT and hydrocarbon (CH 3 T) fractions, and analyzed for the samples collected every 3 d to 14 d during fiscal year 2005. The HT concentration was the highest among the chemical forms analyzed, followed by the HTO and CH 3 T concentrations. The HT and CH 3 T concentrations did not have clear seasonal variation patterns through the HTO concentrations in spring were higher than those in summer. The HT concentration followed the decline previously reported by Mason and Östlund with an apparent half-life of 4.8 y. The apparent and environmental half-lives of CH 3 T were estimated as 9.2 y and 36.5 y, respectively, by combining the present data with literature data. The Intergovernmental Panel on Climate Change used the atmospheric lifetime of 12 y for CH 4 to estimate global warming in its 2007 report. The longer environmental half-life of CH 3 T suggested its supply from other sources than past nuclear weapon testing in the atmosphere. (author)

  19. Methane formation in tritium gas exposed to stainless steel

    International Nuclear Information System (INIS)

    Morris, G.A.

    1977-01-01

    Tests were performed to determine the effect cleanliness of a surface exposed to tritium gas had on methane formation. These tests performed on 304 stainless steel vessels, cleaned in various ways, showed that the methane formation was reduced by the use of various cleaning procedures

  20. Tritium

    International Nuclear Information System (INIS)

    Anon.

    1975-01-01

    The role played the large amount supply of tritium and its effects are broadly reviewed. This report is divided into four parts. The introductory part includes the history of tritium research. The second part deals with the physicochemical properties of tritium and the compounds containing tritium such as tritium water and labeled compounds, and with the isotope effects and self radiation effects of tritium. The third part deals with the tritium production by artificial reaction. Attention is directed to the future productivity of tritium from B, Be, N, C, O, etc. by using the beams of high energy protons or neutrons. The problems of the accepting market and the accuracy of estimating manufacturing cost are discussed. The expansion of production may bring upon the reduction of cost but also a large possibility of social impact. The irradiation problem and handling problem in view of environmental preservation are discussed. The fourth part deals with the use of tritium as a target, as a source of radiation or light, and its utilization for geochemistry. The future development of the solid tritium target capable of elongating the life of neutron sources is expected. The rust thickness of the surface of iron can be measured with the X-ray of Ti-T or Zr-T. The tritium can substitute self-light emission paint or lamp. The tritium is suitable for tracing the movement of sea water and land surface water because of its long half life. (Iwakiri, K.)

  1. Tritium-gas/water-vapor monitor. Tests and evaluation

    International Nuclear Information System (INIS)

    Jalbert, R.A.

    1982-07-01

    A tritium gas/water-vapor monitor was designed and built by the Health Physics Group at the Los Alamos National Laboratory. In its prototype configuration, the monitor took the shape of two separate instruments: a (total) tritium monitor and a water-vapor monitor. Both instruments were tested and evaluated. The tests of the (total) tritium monitor, basically an improved version of the standard flow-through ion-chamber instrument, are briefly reported here and more completely elsewhere. The tests of the water-vapor monitor indicated that the novel approach used to condense water vapor for scintillation counting has a number of serious drawbacks and that further development of the instrument is unwarranted

  2. Evaluation of tritium production rate in a gas-cooled reactor with continuous tritium recovery system for fusion reactors

    Energy Technology Data Exchange (ETDEWEB)

    Matsuura, Hideaki, E-mail: mat@nucl.kyushu-u.ac.jp [Department of Applied Quantum Physics and Nuclear Engineering, Kyushu University, 744 Motooka, Fukuoka 819-0395 (Japan); Nakaya, Hiroyuki; Nakao, Yasuyuki [Department of Applied Quantum Physics and Nuclear Engineering, Kyushu University, 744 Motooka, Fukuoka 819-0395 (Japan); Shimakawa, Satoshi; Goto, Minoru; Nakagawa, Shigeaki [Japan Atomic Energy Agency, 4002 Oarai, Ibaraki 311-1393 (Japan); Nishikawa, Masabumi [Graduate School of Engineering Science, Kyushu University, 6-10-1 Hakozaki, Fukuoka 812-8581 (Japan)

    2013-10-15

    Highlights: • The performance of a gas-cooled reactor as a tritium production system was studied. • A continuous tritium recovery using helium gas was considered. • Gas-cooled reactors with 3 GW output in all can produce ∼6 kg of tritium in a year • Performance of the system was examined for Li{sub 4}SiO{sub 4}, Li{sub 2}TiO{sub 3} and LiAlO{sub 2} compounds. -- Abstract: The performance of a high-temperature gas-cooled reactor as a tritium production with continuous tritium recovery system is examined. A gas turbine high-temperature reactor of 300-MWe (600 MW) nominal capacity (GTHTR300) is assumed as the calculation target, and using the continuous-energy Monte Carlo transport code MVP-BURN, burn-up simulations for the three-dimensional entire-core region of the GTHTR300 were performed. A Li loading pattern for the continuous tritium recovery system in the gas-cooled reactor is presented. It is shown that module gas-cooled reactors with a total thermal output power of 3 GW in all can produce ∼6 kg of tritium maximum in a year.

  3. Study on atmospheric hydrogen enrichment by cryopump method and isotope separation by gas chromatography

    International Nuclear Information System (INIS)

    Taniyama, Yuki; Momoshima, Noriyuki

    2001-01-01

    To obtain the information of source of atmospheric hydrogen tritium an analysis of tritium isotopes is thought to be effective. So an atmospheric hydrogen enrichment apparatus and a cryogenic gas chromatographic column were made. Experiments were carried out to study the performance of cryopump to enrich atmospheric hydrogen and the column to separate hydrogen isotopes that obtained by cryopump method. The cryopump was able to process about 1000 1 atmosphere and the column was able to separate hydrogen isotopes with good resolution. (author)

  4. Tritium activity balance in hairless rats following skin-contact exposure to tritium-gas-contaminated stainless-steel surfaces

    Energy Technology Data Exchange (ETDEWEB)

    Trivedi, A

    1994-06-01

    Studies using animals and human volunteers have demonstrated that the dosimetry for skin-contact exposure to contaminated metal surfaces differs from that for the intake of tritiated water or tritium gas. However, despite the availability of some information on the dosimetry for skin-contact with tritium-gas-contaminated metal surfaces, uncertainties in estimating skin doses remain, because of poor accounting for the applied tritium activity in the body (Eakins et al., 1975; Trivedi, 1993). Experiments on hairless rats were performed to account for the tritium activity applied onto the skin. Hairless rats were contaminated through skin-contact exposure to tritium-gas-contaminated stainless-steel planchets. The activity in the first smear was about 35% of the total removable activity (measured by summing ten consecutive swipes). The amount of tritium applied onto the skin can be approximated by estimating the tritium activity in the first smear removed form the contaminated surfaces. 87 {+-} 9% of the transferred tritium was retained in the exposed skin 30 min post-exposure. 30 min post exposure, the unexposed skin and the carcass retained 8 {+-} 6% and 3 {+-} 2% of the total applied tritium activity, respectively. The percentage of tritium evolved from the body or breathed out was estimated to be 2 {+-} 1% of the total applied activity 30 min post-exposure. It is recommended that to evaluate accurately the amount of tritium transferred to the skin, alternative measurement approaches are required that can directly account for the transferred activity onto the skin. 15 refs., 13 tabs., 7 figs.

  5. Tritium

    International Nuclear Information System (INIS)

    Fiege, A.

    1992-07-01

    This report contains information on chemical and physical properties, occurence, production, use, technology, release, radioecology, radiobiology, dose estimates, radioprotection and legal aspects of tritium. The objective of this report is to provide a reliable data base for the public discussion on tritium, especially with regard to its use in future nuclear fusion plants and its radiological assessment. (orig.) [de

  6. EFFECTS OF TRITIUM GAS EXPOSURE ON THE GLASS TRANSITION TEMPERATURE OF EPDM ELASTOMER AND ON THE CONDUCTIVITY OF POLYANILINE

    Energy Technology Data Exchange (ETDEWEB)

    Clark, E; Marie Kane, M

    2008-12-12

    Four formulations of EPDM (ethylene-propylene diene monomer) elastomer were exposed to tritium gas initially at one atmosphere and ambient temperature for between three and four months in closed containers. Material properties that were characterized include density, volume, mass, appearance, flexibility, and dynamic mechanical properties. The glass transition temperature was determined by analysis of the dynamic mechanical property data per ASTM standards. EPDM samples released significant amounts of gas when exposed to tritium, and the glass transition temperature increased by about 3 C. during the exposure. Effects of ultraviolet and gamma irradiation on the surface electrical conductivity of two types of polyaniline films are also documented as complementary results to planned tritium exposures. Future work will determine the effects of tritium gas exposure on the electrical conductivity of polyaniline films, to demonstrate whether such films can be used as a sensor to detect tritium. Surface conductivity was significantly reduced by irradiation with both gamma rays and ultraviolet light. The results of the gamma and UV experiments will be correlated with the tritium exposure results.

  7. Tritium labelled nucleotides: Heterogeneous metal catalyzed exchange labelling of ATP with tritium gas

    International Nuclear Information System (INIS)

    Jaiswal, D.K.; Morimoto, H.; Williams, P.G.; Wemmer, D.E.

    1991-09-01

    Adenosine 5' triphosphate (ATP) in aqueous solution has been labeled by exchange with tritium gas in the presence of palladium oxide catalyst. Comparison with our experiments using Pd/BaSO 4 as the catalyst shows that we have obtained product with higher specific activity and improved chemical purity. 3 H NMR spectroscopy of the tritiated ATP shows labelling in both the C-8 and C-2 positions, and the integral ratio of these positions was found to vary from 3:1 to 1:1 under different reaction conditions. 5 refs., 1 fig., 2 tabs

  8. Design, fabrication and testing of the gas analysis system for the tritium recovery experiment, TRIO-01

    International Nuclear Information System (INIS)

    Finn, P.A.; Reedy, G.T.; Homa, M.I.; Clemmer, R.G.; Pappas, G.; Slawecki, M.A.; Graczyk, D.G.; Bowers, D.L.; Clemmer, E.D.

    1983-01-01

    The tritium recovery experiment, TRIO-01, required a gas analysis system which detected the form of tritium, the amount of tritium (differential and integral), and the presence and amount of other radioactive species. The system had to handle all contingencies and function for months at a time unattended during weekend operation. The designed system, described herein, consisted of a train of components which could be grouped as desired to match tritium release behavior

  9. Kinetics of the gas-phase tritium oxidation reaction

    International Nuclear Information System (INIS)

    Failor, R.A.

    1989-01-01

    Homogeneous gas-phase kinetics of tritium oxidation (2T 2 + O 2 →2T 2 O) have been studied with a model that accounts explicitly for radiolysis of the major species and the kinetics of the subsequent reactions of ionic, excited-state, and neutral species. Results from model calculations are given for 10 -4 -1.0 mol% T 2 in O 2 (298 K, 1 atm). As the reaction evolves three different mechanisms control T 2 O production, each with a different overall rate expression and a different order with respect to the T 2 concentration. The effects of self-radiolysis of pure T 2 on the tritium oxidation reaction were calculated. Tritium atoms, the primary product of T 2 self-radiolysis, altered the oxidation mechanism only during the first few seconds following the initiation of the T 2 -O 2 reaction. Ozone, an important intermediate in T 2 oxidation, was monitored in-situ by U.V. absorption spectroscopy for 0.01-1.0 mol% T 2 an 1 atm O 2 . The shape of the experimental ozone time profile agreed with the model predictions. As predicted, the measured initial rate of ozone production varied linearly with initial T 2 concentration ([T 2 ] 0.6 o ), but at an initial rate one-third the predicted value. The steady-state ozone concentration ([O 3 ]ss) was predicted to be dependent on [T 2 ] 0.3 o , but the measured value was [T 2 ] 0.6 o , resulting in four times higher [O 3 ]ss than predicted for a 1.0% T 2 -O 2 mixture. Adding H 2 to the T 2 -O 2 mixture, to provide insight into the differences between the radiolytic and chemical behavior of the tritium, produced a greater decrease in [O 3 ]ss than predicted. Adjusting the reaction cell surface-to-volume ratio showed implications of minor surface removal of ozone

  10. Tritium Accounting Stability of a ZrCo Bed with 'In-Bed' Gas Flowing Calorimetry

    International Nuclear Information System (INIS)

    Hayashi, Takumi; Suzuki, Takumi; Yamada, Masayuki; Nishi, Masataka

    2005-01-01

    Zirconium-Cobalt (ZrCo) tritium storage bed with 'in-bed' gas flowing calorimetry has been developed as a self-assaying system for the Tritium Storage and Delivery System of ITER. The basic tritium accounting characteristics have been investigated and practical data on the accounting stability has been accumulated under gram level tritium storage for more than 8 years. The initial sensitivity of tritium was about 0.05 g and the accuracy (standard deviation of repeat measurements: two sigma) was about 0.15 g at full tritium storage of 25 g. This initial accounting performance has been maintained after tritium storage for more than 8 years by keeping constant accounting conditions at each inventory measurement. Almost no aging effect of tritium was found except accumulation of 3 He in the primary ZrCo tritide vessel, which was easily evacuated to keep initial accounting condition before each inventory measurement

  11. Some new techniques in tritium gas handling as applied to metal hydride synthesis

    International Nuclear Information System (INIS)

    Nasise, J.E.

    1988-01-01

    A state-of-the-art tritium Hydriding Synthesis System (HSS) was designed and built to replace the existing system within the Tritium Salt Facility (TSF) at the Los Alamos National Laboratory. This new hydriding system utilizes unique fast-cycling 7.9 mole uranium beds (47.5g of T at 100% loading) and novel gas circulating hydriding furnaces. Tritium system components discussed include fast-cycling uranium beds, circulating gas hydriding furnaces, valves, storage volumes, manifolds, gas transfer pumps, and graphic display and control consoles. Many of the tritium handling and processing techniques incorporated into this system are directly applicable to today's fusion fuel loops. 12 refs., 7 figs

  12. Glovebox atmosphere detritiation process using gas separation membranes

    International Nuclear Information System (INIS)

    Le Digabel, M.; Truan, P.A.; Ducret, D.; Laquerbe, C.; Perriat, P.; Niepce, J.C.; Pelletier, T.

    2003-01-01

    The use of gas separation membranes in atmospheric detritiation systems has been studied. The main advantage of this new process is to reduce the number and/or the size of the equipment in comparison to conventional tritium removal systems. Owing to the constraints linked to tritium handling, the separation performances of several commercial hollow fiber organic membranes have been analyzed, under various operating conditions, with hydrogen/nitrogen or deuterium/nitrogen mixtures. The experiments are performed with small quantities of hydrogen or deuterium (5000 ppm). The experimental results allow to evaluate the separation efficiency of these membranes and to determine the appropriate operating conditions to apply to a membrane detritiation process

  13. The JET gas baking plant for DT operation and analysis of tritium permeation and baking gas activation in DTE1

    Energy Technology Data Exchange (ETDEWEB)

    Pearce, R.J.H.; Andrew, P.; Bryan, S.; Hemmrich, J.L. [JET Joint Undertaking, Abingdon, Oxon (United Kingdom)

    1998-07-01

    The JET gas baking plant allows the vacuum vessel to be heated for conditioning and plasma operations. The vessel was maintained at 320 deg. C for the JET DT experiments (DTE 1). The design of the plant is outlined with particular reference to the features to provide compatibility with tritium operations. The experience of baking gas activation and tritium permeation into the plant are given, Developmentsto reduce the tritium permeation out of the vessel are considered. (authors)

  14. Study of atmospheric tritium transfers in lettuce: kinetic study, equilibrium and organic incorporation during a continuous atmospheric exposure

    International Nuclear Information System (INIS)

    Boyer, C.

    2009-01-01

    This thesis has explored the mechanisms of tritium 'absorption and incorporation in a human-consumed plant, lettuce (Lactuca sativa L.), due to atmospheric exposure. Foliar uptake appears to play a key role in absorption of tritium as tissue free water tritium. Whatever the development stage and the light conditions, the specific activity in tissue free water reaches that of water vapour in air in several hours. The specific activity ratio is then about 0, 4. The time to reach equilibrium in soil is over 24 hours in most cases: the specific activity ratio ranges then 0, 01 to 0, 26. Incorporation rate of tissue free water tritium as organically-bound tritium has been estimated to 0, 13 to 0, 16 % h-l in average over the growing period of the plant, but marked variations are observed during growth. In particular, a significant increase appeared at the exponential growth stage. Deposition and diffusion of tritium in soil lead to significant OBT activities in soil. Results globally indicate equilibrium between the different environmental compartments (air, soil, plant). However, some experiments have revealed high OBT concentrations regarding atmospheric level exposure and ask for a possible phenomenon of local tritium accumulation in OBT for particular conditions of exposure. (author) [fr

  15. Catalyst study for the decontamination of glove-box atmospheres containing tritium at MPC levels

    International Nuclear Information System (INIS)

    Chobot, J.; Montel, J.; Sannier, J.

    1988-01-01

    The BEATRICE loop was designed for studying the conversion of tritium at very low activity levels using catalytic oxidation followed by water trapping. The purpose is to study kinetic parameters required for the design of the NET tritium cleanup system with the two main objectives to operate without isotopic swamping and to determine the ability of efficient conversion at room temperature. From experiments carried out between 20 and 250 0 C it is concluded that two palladium/alumina and platinum/alumina catalysts are very efficient in removing tritium from contaminated gas mixtures down to a few MPC levels without isotopic swamping and even at room temperature. However at room temperature, in relation to tritium species trapped on the catalyst surface a progressive deactivation with time occurs. This phenomenon may be a concern for process efficiency and tritium inventory and regeneration conditions have to be determined in order to demonstrate industrial feasibility of operating at room temperature

  16. Catalyst study for the decontamination of glove-boxe atmospheres containing tritium at MPC levels

    International Nuclear Information System (INIS)

    Chabot, J.; Montel, J.; Sannier, J.

    1988-01-01

    The BEATRICE loop was designed for studying the conversion of tritium at very low activity levels using catalytic oxidation followed by water trapping. The purpose is to study kinetic parameters required for the design of the NET tritium clean-up system with the two main objectives to operate without isotopic swamping and to determine the ability of efficient conversion at room temperature. From experiments carried out between 20 and 250 0 C it is concluded that two palladium/alumina and platinum/alumina catalysts are very efficient in removing tritium from contaminated gas mixtures down to a few MPC levels without isotopic swamping and even at room temperature. However at room temperature, in relation to tritium species trapped on the catalyst surface a progressive deactivation with time occurs. This phenomenon may be a concern for process efficiency and tritium inventory and best regeneration conditions have to be determined in order to demonstrate industrial feasibility of operating at room temperature

  17. High pressure deuterium-tritium gas target vessels for muon-catalyzed fusion experiments

    International Nuclear Information System (INIS)

    Caffrey, A.J.; Spaletta, H.W.; Ware, A.G.; Zabriskie, J.M.; Hardwick, D.A.; Maltrud, H.R.; Paciotti, M.A.

    1989-01-01

    In experimental studies of muon-catalyzed fusion, the density of the hydrogen gas mixture is an important parameter. Catalysis of up to 150 fusions per muon has been observed in deuterium-tritium gas mixtures at liquid hydrogen density; at room temperature, such densities require a target gas pressure of the order of 1000 atmospheres (100 MPa, 15,000 psi). We report here the design considerations for hydrogen gas target vessels for muon-catalyzed fusion experiments that operate at 1000 and 10,000 atmospheres. The 1000 atmosphere high pressure target vessels are fabricated of Type A-286 stainless steel and lined with oxygen-free, high-conductivity (OFHC) copper to provide a barrier to hydrogen permeation of the stainless steel. The 10,000 atmosphere ultrahigh pressure target vessels are made from 18Ni (200 grade) maraging steel and are lined with OFHC copper, again to prevent hydrogen permeation of the steel. In addition to target design features, operating requirements, fabrication procedures, and secondary containment are discussed. 13 refs., 3 figs., 1 tab

  18. Measured tritium in groundwater related to atmospheric releases from the Marcoule nuclear site

    International Nuclear Information System (INIS)

    Levy, F.; Clech, A.; Crochet, P.

    1996-01-01

    Tritium is released into the atmosphere during normal operation from the industrial facilities operated by COGEMA at Marcoule; over a 1 5-year period covered by this study (1979-1994) the quantities ranged from 4940 to 520 TBq·yr -1 . Atmospheric release in rainy weather results in tritium migration into the ground water by a series of mechanisms associated with the water cycle. COGEMA monitors the ground water by means of bore holes. Atmospheric monitoring is also routinely performed; data on the tritium activity concentration in the air and rainwater are available for the same time period. A simplified observation suggests a relation between the atmospheric tritium release and the ground water radioactivity. In 1994, the activity ranged from 100 to 200 Bq·l -1 in the boreholes located 1 km and 2 km downwind from the point of release, diminishing with the distance to less than 20 Bq·l -1 at about 3 km. The authors attempted to model two types of transfers: atmospheric transfer from the release chimney to the borehole, and transfer in the alluvial ground water. The aquifer comprises the alluvial deposits forming the Codolet plain extending to the south of Marcoule, downwind from the point of atmospheric tritium release. The hydrogeology of the entire Marcoule site has been described in previous studies by the French bureau of geological and mineralogical research (BRGM) and ANTEA. (author)

  19. Estimating Tritium Fluxes from the Shallow Unsaturated Zone to the Atmosphere in an Arid Environment Dominated by Creosote Bush (USGS-ADRS)

    Science.gov (United States)

    Garcia, C. A.; Andraski, B. J.; Wheatcraft, S. W.; Johnson, M. J.; Michel, R. L.; Stonestrom, D. A.

    2006-12-01

    Understanding the transport and fate of tritium is essential when evaluating options for low-level radioactive waste (LLRW) isolation. The magnitude and spatio-temporal variability of tritium transport from the shallow unsaturated zone to the atmosphere are being investigated adjacent to a LLRW facility at the U.S. Geological Survey's Amargosa Desert Research Site (ADRS) in Southern Nevada. Site and community-scale tritium fluxes from the subsurface to the atmosphere were quantified using a simple gas-phase diffusive loading approach combining evaporation and transpiration fluxes with mass fractions of gas-phase tritium concentrations. A Priestly-Taylor model, calibrated with quarterly bare-soil evaporation measurements, was used to estimate continuous bare-soil evaporation from measured continuous eddy-covariance evapotransporation. Continuous transpiration was computed as the difference between measured evapotranspiration and estimated bare-soil evaporation. Tritium concentrations in plant water and soil-water vapor were measured along two transects perpendicular to the LLRW using azeotropic distillation of creosote bush (Larrea tridentata) foliage and soil vapor extraction from 0.5 and 1.5 m depths below land surface. A preliminary daily tritium flux estimate at a single plant site was 1.66 × 10-11 gm-2. Spatio- temporal variability over a 75-ha area and 2-yr period will be quantified using a combination of tritium concentration maps and continuous evaporation and transpiration flux estimates. Quantifying tritium fluxes from the shallow unsaturated zone to the atmosphere on a site and community-scale will improve knowledge and understanding of vertical contaminant transport in arid environments.

  20. Levels of tritium in soils and vegetation near Canadian nuclear facilities releasing tritium to the atmosphere: implications for environmental models

    International Nuclear Information System (INIS)

    Thompson, P.A.; Kwamena, N.-O.A.; Ilin, M.; Wilk, M.; Clark, I.D.

    2015-01-01

    Concentrations of organically bound tritium (OBT) and tritiated water (HTO) were measured over two growing seasons in vegetation and soil samples obtained in the vicinity of four nuclear facilities and two background locations in Canada. At the background locations, with few exceptions, OBT concentrations were higher than HTO concentrations: OBT/HTO ratios in vegetation varied between 0.3 and 20 and values in soil varied between 2.7 and 15. In the vicinity of the four nuclear facilities OBT/HTO ratios in vegetation and soils deviated from the expected mean value of 0.7, which is used as a default value in environmental transfer models. Ratios of the OBT activity concentration in plants ([OBT] plant ) to the OBT activity concentration in soils ([OBT] soil ) appear to be a good indicator of the long-term behaviour of tritium in soil and vegetation. In general, OBT activity concentrations in soils were nearly equal to OBT activity concentrations in plants in the vicinity of the two nuclear power plants. [OBT] plant /[OBT] soil ratios considerably below unity observed at one nuclear processing facility represents historically higher levels of tritium in the environment. The results of our study reflect the dynamic nature of HTO retention and OBT formation in vegetation and soil during the growing season. Our data support the mounting evidence suggesting that some parameters used in environmental transfer models approved for regulatory assessments should be revisited to better account for the behavior of HTO and OBT in the environment and to ensure that modelled estimates (e.g., plant OBT) are appropriately conservative. - Highlights: • We measured tritium in soils and plants near four nuclear facilities in Canada. • OBT/HTO ratios in plants are higher than default value in environmental models. • OBT/HTO ratios in background soils reflect historically higher atmospheric tritium. • Implications for environmental transfer models are discussed

  1. Tritium concentration analysis in atmospheric precipitation in Serbia.

    Science.gov (United States)

    Janković, Marija M; Janković, Bojan Ž; Todorović, Dragana J; Ignjatović, Ljubiša M

    2012-01-01

    Tritium activity concentration were monitored in monthly precipitation at five locations in Serbia (Meteorological Station of Belgrade at Zeleno Brdo, Vinča Institute of Nuclear Sciences, Smederevska Palanka, Kraljevo and Niš) over 2005, using electrolytic enrichment and liquid scintillation counting. The obtained concentrations ranged from 3.36 to 127.02 TU. The activity values obtained in samples collected at Zeleno Brdo were lower or close to the minimum detectable activity (MDA), which has a value of 3.36 TU. Significantly higher tritium levels were obtained in samples collected in Vinča Institute of Nuclear Sciences compared with samples from the other investigated locations. Amount of precipitation were also recorded. A good linear correlation (r = 0.75) for Zeleno Brdo and VINS between their tritium activity was obtained. It was found that the value of the symmetrical index n (which indicates the magnitude of tritium content changes with time (months) through its second derivative) is the highest for Vinča Institute of Nuclear Sciences compared to other locations, which is in accordance with the fact that the highest concentrations of tritium were obtained in the samples from the cited place.

  2. Preparation of alveolate hydrophobic catalyst for tritium waste gas treatment

    International Nuclear Information System (INIS)

    Yang, Yong; Peng, Shuming; Wang, Heyi; Du, Yang; Li, Jiamao

    2016-01-01

    Highlights: • The catalyst is hydrophobic, it will not be poisoned by steam in room air at room temperature which is better than Pt-Al 2 O 3 . • At room temperature, the conversion of low concentration of H2 and tritium gas in room air over the catalyst is high. • The air resistance of catalyst is much lower than graininess Pt-Al 2 O 3 . • It is inorganic and will not burn. - Abstract: To prepare a catalyst for the detritiation of waste gases at high flow rates, a heat-resistant hydrophobic zeolitic molecular sieve coating was synthesized on the surface of alveolate cordierite by hydrothermal processing. The alveolate hydrophobic catalyst prepared from the support was essentially waterproof and not easily poisoned by moisture. At room temperature, the conversion of low concentrations of H 2 in humid air over the catalyst was higher than 95% at different space velocities (0–16,000 h −1 ) and different relative humidities. The reaction rate constant of the oxidation of tritium over alveolate hydrophobic catalyst is 0.182 s −1 at 293.3 K–293.7 K and 59%–60% RH, it is much higher than the catalyst of reference honeycomb catalyst.

  3. Tritium emissions reduction facility (TERF)

    International Nuclear Information System (INIS)

    Lamberger, P.H.; Hedley, W.H.

    1993-01-01

    Tritium handling operations at Mound include production of tritium-containing devices, evaluation of the stability of tritium devices, tritium recovery and enrichment, tritium process development, and research. In doing this work, gaseous process effluents containing 400,000 to 1,000,000 curies per year of tritium are generated. These gases must be decontaminated before they can be discharged to the atmosphere. They contain tritium as elemental hydrogen, as tritium oxide, and as tritium-containing organic compounds at low concentrations (typically near one ppm). The rate at which these gases is generated is highly variable. Some tritium-containing gas is generated at all times. The systems used at Mound for capturing tritium from process effluents have always been based on the open-quotes oxidize and dryclose quotes concept. They have had the ability to remove tritium, regardless of the form it was in. The current system, with a capacity of 1.0 cubic meter of gas per minute, can effectively remove tritium down to part-per-billion levels

  4. Tritium distribution in the environment in the vicinity of a chronic atmospheric source-assessment of the steady state hypothesis

    International Nuclear Information System (INIS)

    Murphy, C.E. Jr.; Bauer, L.R.; Zeigler, C.C.

    1990-01-01

    The Savannah River Site (SRS) is a major radionuclide production center. Tritium has been released to the atmosphere over the 36 year period of operation. The tritiated water concentration of the atmosphere, rain, vegetation and food have been routinely monitored during this period. Special studies have been made of tritium in soils and in the organic fractions of these same materials. The available data suggest that the average tritium concentration in the components of the terrestrial environment have approached a steady state with the two main sources of tritium, rainfall and atmospheric water vapor

  5. Automatic isotope gas analysis of tritium labelled organic materials Pt. 1

    International Nuclear Information System (INIS)

    Gacs, I.; Mlinko, S.

    1978-01-01

    A new automatic procedure developed to convert tritium in HTO hydrogen for subsequent on-line gas counting is described. The water containing tritium is introduced into a column prepared from molecular sieve-5A and heated to 550 deg C. The tritium is transferred by isotopic exchange into hydrogen flowing through the column. The radioactive gas is led into an internal detector for radioactivity measurement. The procedure is free of memory effects, provides quantitative recovery with analytical reproducibility better than 0.5% rel. at a preset number of counts. The experimental and analytical results indicate that isotopic exchange between HTO and hydrogen over a column prepared from alumina or molecular sieve-5A can be successfully applied for the quantitative transfer of tritium from HTO into hydrogen for on-line gas countinq. This provides an analytical procedure for the automatic determination of tritium in water with an analytical reproducibility better than 0.5% rel. The exchange process will also be suitable for rapid tritium transfer from water formed during the decomposition of tritium-labelled organic compounds or biological materials. The application of the procedure in automatic isotope gas analysis of organic materials labelled with tritium will be described in subsequent papers (Parts II and III). (T.G.)

  6. Detection of atmospheric tritium by scintillation. Variations in its concentration in France

    International Nuclear Information System (INIS)

    Bibron, R.

    1964-06-01

    The tritium released into the atmosphere as a result of the explosion of thermonuclear devices is a useful radioactive tracer for the study of certain geophysical problems. The low concentrations found however call for the use of extremely sensitive detectors. Two detection methods using liquid scintillators are described. In the first method, the sample is introduced into the scintillator in liquid form, after prior concentration of the tritium by electrolysis. In the second method the tritium is incorporated into the scintillator solvent molecule by chemical synthesis. In the last part of the report are examined the variations in the tritium concentration in rain-water and of the free hydrogen in the air in France. A discussion is then made of the seasonal variations in the case of rain-water and these are compared to the variations in the strontium-90 concentrations. (author) [fr

  7. High concentration tritium gas measurement with small volume ionization chambers for fusion fuel gas monitors

    International Nuclear Information System (INIS)

    Uda, Tatsuhiko; Okuno, Kenji; Matsuda, Yuji; Naruse, Yuji

    1991-01-01

    To apply ionization chambers to fusion fuel gas processing systems, high concentration tritium gas was experimentally measured with small volume 0.16 and 21.6 cm 3 ionization chambers. From plateau curves, the optimum electric field strength was obtained as 100∼200 V/cm. Detection efficiency was confirmed as dependent on the ionization ability of the filled gas, and moreover on its stopping power, because when the range of the β-rays was shortened, the probability of energy loss by collisions with the electrode and chamber wall increased. Loss of ions by recombination was prevented by using a small volume ionization chamber. For example the 0.16 cm 3 ionization chamber gave measurement with linearity to above 40% tritium gas. After the tritium gas measurements, the concentration levels inside the chamber were estimated from their memory currents. Although more than 1/4,000 of the maximum, current was observed as a memory effect, the smaller ionization chamber gave a smaller memory effect. (author)

  8. Relation between the tritium in continuous atmospheric release and the tritium contents of fruits and tubers.

    Science.gov (United States)

    Korolevych, V Y; Kim, S B

    2013-04-01

    Concentrations of organically bound tritium (OBT) and tissue-free water tritium (TFWT, also referred to as HTO) in fruits and tubers were measured at a garden plot in the vicinity of the source of chronic airborne tritium emissions during the 2008, 2010, and 2011 growing seasons. A continuous record of HTO concentration in the air moisture was reconstructed from the continuous record of Ar-41 ambient gamma radiation, as well as from frequent measurements of air HTO by active samplers at the garden plot and Ar-41 and air HTO monitoring data from the same sector. Performed measurements were used for testing the modified Specific Activity (SA) model based on the assumption that the average air HTO during the pod-filling period provides an appropriate basis for estimating the levels of OBT present in pods, fruits and tubers. It is established that the relationship between the OBT of fruits and tubers and the average air HTO from a 15-20 day wide window centred at the peak of the pod-filling period is consistent throughout the three analysed years, and could be expressed by the fruit or tuber's OBT to air-HTO ratio of 0.93 ± 0.21. For all three years, the concentration of HTO in fruits and tubers was found to be related to levels of HTO in the air, as averaged within a 3-day pre-harvest window. The variability in the ratio of plant HTO to air HTO appears to be three times greater than that for the OBT of the fruits and tubers. It is concluded that the OBT of fruits and tubers adequately follows an empirical relationship based on the average level of air HTO from the pod-filling window, and therefore is clearly in line with the modified SA approach. Crown Copyright © 2012. Published by Elsevier Ltd. All rights reserved.

  9. Catalyst study for the decontamination of atmospheres containing few traces of tritium

    International Nuclear Information System (INIS)

    Chabot, J.; Montel, J.; Sannier, J.

    1988-01-01

    The conversion of tritium at very low activity level using catalytic oxidation followed by water trapping is studied in the loop BEATRICE in order to measure kinetic parameters required for the design of the NET tritium clean-up system. Two precious-metal catalysts (Pd/alumina and Pt/alumina) are very efficient in removing tritium from contaminated gas mixtures down to a few MPC level at low temperatures, without need of isotopic swamping. However at room temperature, the trapping of tritium species on the catalyst surface gives rise to a progressive deactivation with time. Best regeneration conditions have to be determined in order to demonstrate industrial feasibility of operating at low temperatures

  10. Tritium permeation behavior through pyrolytic carbon in tritium production using high-temperature gas-cooled reactor for fusion reactors

    Directory of Open Access Journals (Sweden)

    H. Ushida

    2016-12-01

    Full Text Available Under tritium production method using a high-temperature gas-cooled reactor loaded Li compound, Li compound has to be coated by ceramic materials in order to suppress the spreading of tritium to the whole reactor. Pyrolytic carbon (PyC is a candidate of the coating material because of its high resistance for gas permeation. In this study, hydrogen permeation experiments using a PyC-coated isotropic graphite tube were conducted and hydrogen diffusivity, solubility and permeability were evaluated. Tritium permeation behavior through PyC-coated Li compound particles was simulated by using obtained data. Hydrogen permeation flux through PyC in a steady state is proportional to the hydrogen pressure and is larger than that through Al2O3 which is also candidate coating material. However, total tritium leak within the supposed reactor operation period through the PyC-coated Li compound particles is lower than that through the Al2O3-coated ones because the hydrogen absorption capacity in PyC is considerably larger than that in Al2O3.

  11. A versatile model for tritium transfer from atmosphere to plant and soil

    International Nuclear Information System (INIS)

    Melintescu, A.; Galeriu, D.

    2004-01-01

    The need to increase the predictive power of risk assessment for large tritium releases implies a process level approach for model development. Tritium transfer for atmosphere to plant and the conversion in organically bound tritium depend strongly on plant characteristics, season, and meteorological conditions.In order to cope with this large variability and to avoid also, expensive calibration experiments, we developed a model using knowledge of plant physiology, agro-meteorology, soil sciences, hydrology, and climatology. The transfer of tritiated water to plant is modelled with resistance approach including sparse canopy. The canopy resistance is modelled using Jarvis-Calvet approach modified in order to directly use the canopy photosynthesis rate.The crop growth model WOFOST is used for photosynthesis rate both for canopy resistance and formation of organically bound tritium, also. Using this formalism, the tritium transfer parameters are directly linked to known processes and parameters from agricultural sciences. The model predictions for tritium in wheat are closed to a factor two to experimental data without any calibration. The model also is tested for rice and soya bean and can be applied for various plants and environmental conditions. For sparse canopy the model uses coupled equations between soil and plants. (author)

  12. Tritium confinement in a new tritium processing facility at the Savannah River Site

    International Nuclear Information System (INIS)

    Heung, L.K.; Owen, J.H.; Hsu, R.H.; Hashinger, R.F.; Ward, D.E.; Bandola, P.E.

    1991-01-01

    A new tritium processing facility, named the Replacement Tritium Facility (RTF), has been completed and is being prepared for startup at the Savannah River Site (SRS). The RTF has the capability to recover, purify and separate hydrogen isotopes from recycled gas containers. A multilayered confinement system is designed to reduce tritium losses to the environment. This confinement system is expected to confine and recover any tritium that might escape the process equipment, and to maintain the tritium concentration in the nitrogen glovebox atmosphere to less than 10 -2 μCi/cc tritium

  13. The ITER tritium systems

    International Nuclear Information System (INIS)

    Glugla, M.; Antipenkov, A.; Beloglazov, S.; Caldwell-Nichols, C.; Cristescu, I.R.; Cristescu, I.; Day, C.; Doerr, L.; Girard, J.-P.; Tada, E.

    2007-01-01

    ITER is the first fusion machine fully designed for operation with equimolar deuterium-tritium mixtures. The tokamak vessel will be fuelled through gas puffing and pellet injection, and the Neutral Beam heating system will introduce deuterium into the machine. Employing deuterium and tritium as fusion fuel will cause alpha heating of the plasma and will eventually provide energy. Due to the small burn-up fraction in the vacuum vessel a closed deuterium-tritium loop is required, along with all the auxiliary systems necessary for the safe handling of tritium. The ITER inner fuel cycle systems are designed to process considerable and unprecedented deuterium-tritium flow rates with high flexibility and reliability. High decontamination factors for effluent and release streams and low tritium inventories in all systems are needed to minimize chronic and accidental emissions. A multiple barrier concept assures the confinement of tritium within its respective processing components; atmosphere and vent detritiation systems are essential elements in this concept. Not only the interfaces between the primary fuel cycle systems - being procured through different Participant Teams - but also those to confinement systems such as Atmosphere Detritiation or those to fuelling and pumping - again procured through different Participant Teams - and interfaces to buildings are calling for definition and for detailed analysis to assure proper design integration. Considering the complexity of the ITER Tritium Plant configuration management and interface control will be a challenging task

  14. Protection against tritium radiations

    International Nuclear Information System (INIS)

    Bal, Georges

    1964-05-01

    This report presents the main characteristics of tritium, describes how it is produced as a natural or as an artificial radio-element. It outlines the hazards related to this material, presents how materials and tools are contaminated and decontaminated. It addresses the issue of permissible maximum limits: factors of assessment of the risk induced by tritium, maximum permissible activity in body water, maximum permissible concentrations in the atmosphere. It describes the measurement of tritium activity: generalities, measurement of gas activity and of tritiated water steam, tritium-induced ionisation in an ionisation chamber, measurement systems using ionisation chambers, discontinuous detection of tritium-containing water in the air, detection of surface contamination [fr

  15. The design, fabrication and testing of the gas analysis system for the tritium recovery experiment, TRIO-01

    International Nuclear Information System (INIS)

    Finn, P.A.; Bowers, D.L.; Clemmer, E.D.; Clemmer, R.G.; Graczyk, D.G.; Homa, M.I.; Pappas, G.; Reedy, G.T.; Slawecki, M.A.

    1983-01-01

    The tritium recovery experiment, TRIO-01, required a gas analysis system which detected the form of tritium, the amount of tritium (differential and integral), and the presence and amount of other radioactive species. The system had to handle all contingencies and function for months at a time; unattended during weekend operation. The designed system, described herein, consisted of a train of components which could be grouped as desired to match tritium release behavior

  16. Tritium monitoring in the GCFR sweep gas fuel irradiation capsule BG-10

    International Nuclear Information System (INIS)

    Gat, U.; Pruitt, M.E.; Longest, A.W.; Epstein, B.D.

    1980-01-01

    The release of tritium and its transport pathways were studied in a vented, pressure-equalized fuel rod which simulated a fuel rod in a Gas-Cooled Fast Reactor (GCFR). The purpose was to determine the fraction of total tritium production transported via the various pathways and to determine its chemical form (tritiated hydrogen or water). It was concluded that the fuel rod and its effluent venting lines retained low concentrations of HT (or T 2 ) and any HTO (or T 2 O) present. However, the addition of 1% hydrogen to the helium carrier gas quantitatively eluted the tritium from the charcoal trap integral to the fuel rod and from the effluent lines. The chemical composition of the tritium arriving at the monitoring system could be determined by means of converters which convert HT to HTO and vice versa. Ht was the dominant species in the samples measured

  17. Study on a method for loading a Li compound to produce tritium using high-temperature gas-cooled reactor

    Energy Technology Data Exchange (ETDEWEB)

    Nakaya, Hiroyuki, E-mail: nakaya@nucl.kyushu-u.ac.jp [Department of Applied Quantum Physics and Nuclear Engineering, Kyushu University, 744 Motooka, Fukuoka 8190395 (Japan); Matsuura, Hideaki [Department of Applied Quantum Physics and Nuclear Engineering, Kyushu University, 744 Motooka, Fukuoka 8190395 (Japan); Katayama, Kazunari [Department of Advanced Energy Engineering Science, Kyushu University, 6-1 Kasuga-koen, Kasuga 8168580 (Japan); Goto, Minoru; Nakagawa, Shigeaki [Japan Atomic Energy Agency, 4002 Oarai, Ibaraki (Japan)

    2015-10-15

    Highlights: • Tritium production by a high-temperature gas-cooled reactor was studied. • The loading method considering tritium outflow suppression was estimated. • A reactor with 600 MWt produced 400–600 g of tritium for 180 days. • A possibility that tritium outflow can be sufficiently suppressed was shown. - Abstract: Tritium production using high-temperature gas-cooled reactors and its outflow from the region loading Li compound into the helium coolant are estimated when considering the suppression of tritium outflow. A Li rod containing a cylindrical Li compound placed in an Al{sub 2}O{sub 3} cladding tube is assumed as a method for loading Li compound. A gas turbine high-temperature reactor of 300 MW electrical nominal capacity (GTHTR300) with 600 MW thermal output power is considered and modeled using the continuous-energy Monte Carlo transport code MVP-BURN, where burn-up simulations are carried out. Tritium outflow is estimated from equilibrium solution for the tritium diffusion equation in the cladding tube. A GTHTR300 can produce 400–600 g of tritium over a 180-day operation using the chosen method of loading the Li compound while minimizing tritium outflow from the cladding tube. Optimizing tritium production while suppressing tritium outflow is discussed.

  18. Detection of atmospheric tritium by scintillation. Variations in its concentration in France; Detection du tritium atmospherique par scintillation. Evolution de sa concentration en France

    Energy Technology Data Exchange (ETDEWEB)

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

    1964-06-01

    The tritium released into the atmosphere as a result of the explosion of thermonuclear devices is a useful radioactive tracer for the study of certain geophysical problems. The low concentrations found however call for the use of extremely sensitive detectors. Two detection methods using liquid scintillators are described. In the first method, the sample is introduced into the scintillator in liquid form, after prior concentration of the tritium by electrolysis. In the second method the tritium is incorporated into the scintillator solvent molecule by chemical synthesis. In the last part of the report are examined the variations in the tritium concentration in rain-water and of the free hydrogen in the air in France. A discussion is then made of the seasonal variations in the case of rain-water and these are compared to the variations in the strontium-90 concentrations. (author) [French] Le tritium introduit dans l'atmosphere par les explosions d'armes thermonucleaires est un traceur radioactif Interessant pour l'etude de certains problemes de geophysique. Les faibles concentrations rencontrees obligent toutefois a utiliser des detecteurs extremement sensibles. On decrit deux methodes de detection utilisant des scintillateurs liquides. Dans la premiere methode, l'echantillon est introduit dans le scintillateur, sous forme aqueuse, apres une concentration prealable du tritium par electrolyse. Dans la seconde methode, le tritium est incorpore a la molecule du solvant du scintillateur par synthese chimique. Dans la derniere partie du rapport, on examine l'evolution de la concentration du tritium dans les eaux de precipitation et l'hydrogene libre de l'air en France. On discute ensuite les variations saisonnieres dans le cas des eaux de precipitation et on les compare aux variations du strontium 90. (auteur)

  19. Detection of atmospheric tritium by scintillation. Variations in its concentration in France; Detection du tritium atmospherique par scintillation. Evolution de sa concentration en France

    Energy Technology Data Exchange (ETDEWEB)

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

    1964-06-01

    The tritium released into the atmosphere as a result of the explosion of thermonuclear devices is a useful radioactive tracer for the study of certain geophysical problems. The low concentrations found however call for the use of extremely sensitive detectors. Two detection methods using liquid scintillators are described. In the first method, the sample is introduced into the scintillator in liquid form, after prior concentration of the tritium by electrolysis. In the second method the tritium is incorporated into the scintillator solvent molecule by chemical synthesis. In the last part of the report are examined the variations in the tritium concentration in rain-water and of the free hydrogen in the air in France. A discussion is then made of the seasonal variations in the case of rain-water and these are compared to the variations in the strontium-90 concentrations. (author) [French] Le tritium introduit dans l'atmosphere par les explosions d'armes thermonucleaires est un traceur radioactif Interessant pour l'etude de certains problemes de geophysique. Les faibles concentrations rencontrees obligent toutefois a utiliser des detecteurs extremement sensibles. On decrit deux methodes de detection utilisant des scintillateurs liquides. Dans la premiere methode, l'echantillon est introduit dans le scintillateur, sous forme aqueuse, apres une concentration prealable du tritium par electrolyse. Dans la seconde methode, le tritium est incorpore a la molecule du solvant du scintillateur par synthese chimique. Dans la derniere partie du rapport, on examine l'evolution de la concentration du tritium dans les eaux de precipitation et l'hydrogene libre de l'air en France. On discute ensuite les variations saisonnieres dans le cas des eaux de precipitation et on les compare aux variations du strontium 90. (auteur)

  20. Lifetime and shelf life of sealed tritium-filled plasma focus chambers with gas generator

    Directory of Open Access Journals (Sweden)

    B.D. Lemeshko

    2017-11-01

    Full Text Available The paper describes the operation features of plasma focus chambers using deuterium–tritium mixture. Handling tritium requires the use of sealed, vacuum-tight plasma focus chambers. In these chambers, there is an accumulation of the impurity gases released from the inside surfaces of the electrodes and the insulator while moving plasma current sheath inside chambers interacting with β-electrons generated due to the decay of tritium. Decay of tritium is also accompanied by the accumulation of helium. Impurities lead to a decreased yield of neutron emission from plasma focus chambers, especially for long term operation. The paper presents an option of absorption type gas generator in the chamber based on porous titanium, which allows to significantly increase the lifetime and shelf life of tritium chambers. It also shows the results of experiments on the comparison of the operation of sealed plasma focus chambers with and without the gas generator. Keywords: Plasma focus, Neutron yield, Tritium-filled plasma focus chambers, PACS Codes: 29.25.-v, 52.58.Lq

  1. Tritium generation and neutron measurements in Pd-Si under high deuterium gas pressure

    International Nuclear Information System (INIS)

    Claytor, T.N.; Tuggle, D.G.; Menlove, H.O.

    1991-01-01

    This paper summarizes some of the methods applicable for low level tritium detection needed in the search for anomalous fusion in metal hydrides. It is also intended to further detail our tritium and neutron results that have been obtained with the Pd-Si-D system, originally presented at earlier workshops. A measure of reproducibility that was not evident in our previous work has been achieved partially due to the better detection sensitivity afforded by the use of low tritium deuterium and partially from the fact that the foil-wafer cells can be made with nearly identical electrical characteristics. This reproducibility has allowed us to narrow the optimum conditions for the experiment. While this experiment is rather different from the ''standard'' electrolytic cell or the Ti gas hydride experiment, similarities exist in that non equilibrium conditions are sought and the tritium generation levels are low and neutron emission is extremely weak. In contrast to many electrochemical cell experiments, the system used in these experiments is completely sealed during operation and uses no electrolyte. The major improvements to the experiment have been the use of vary low tritium deuterium for the hydriding and the replacement of the aluminum neutron counter tubes with ones of stainless steel. These changes have resulted in pronounced improvements to the detection systems since the background tritium level in the gas has been reduced by a factor of 300 and the neutron background has been decreased by a factor of 14. 16 refs., 8 figs., 1 tab

  2. Automatic isotope gas analysis of tritium labelled organic materials Pt. 3

    International Nuclear Information System (INIS)

    Gacs, I.; Mlinko, S.; Payer, K.; Otvos, L.; Banfi, D.; Palagyi, T.

    1978-01-01

    An isotope analytical procedure and an automatic instrument developed for the determination of tritium in organic compounds and biological materials by internal gas counting are described. The sample is burnt in a stream of oxygen and the combustion products including water vapour carrying the tritium are led onto a column of molecular sieve-5A heated to 550 deg C. Tritium is retained temporarily on the column, then transferred into a stream of hydrogen by isotope exchange. After addition of butane, the tritiated hydrogen is led into an internal detector and enclosed there for radioactivity measurement. The procedure, providing quantitative recovery, is completed in five minutes. It is free of memory effect and suitable for the determination of tritium in a wide range of organic compounds and samples of biological origin. (author)

  3. An overview of organically bound tritium experiments in plants following a short atmospheric HTO exposure.

    Science.gov (United States)

    Galeriu, D; Melintescu, A; Strack, S; Atarashi-Andoh, M; Kim, S B

    2013-04-01

    The need for a less conservative, but reliable risk assessment of accidental tritium releases is emphasized in the present debate on the nuclear energy future. The development of a standard conceptual model for accidental tritium releases must be based on the process level analysis and the appropriate experimental database. Tritium transfer from atmosphere to plants and the subsequent conversion into organically bound tritium (OBT) strongly depends on the plant characteristics, seasons, and meteorological conditions, which have a large variability. The present study presents an overview of the relevant experimental data for the short term exposure, including the unpublished information, also. Plenty of experimental data is provided for wheat, rice, and soybean and some for potato, bean, cherry tomato, radish, cabbage, and tangerine as well. Tritiated water (HTO) uptake by plants during the daytime and nighttime has an important role in further OBT synthesis. OBT formation in crops depends on the development stage, length, and condition of exposure. OBT translocation to the edible plant parts differs between the crops analyzed. OBT formation during the nighttime is comparable with that during the daytime. The present study is a preliminary step for the development of a robust model of crop contamination after an HTO accidental release. Copyright © 2012 Elsevier Ltd. All rights reserved.

  4. Core configuration of a gas-cooled reactor as a tritium production device for fusion reactor

    Energy Technology Data Exchange (ETDEWEB)

    Nakaya, H., E-mail: nakaya@nucl.kyushu-u.ac.jp [Department of Applied Quantum Physics and Nuclear Engineering, Kyushu University, 744 Motooka, Fukuoka 8190395 (Japan); Matsuura, H.; Nakao, Y. [Department of Applied Quantum Physics and Nuclear Engineering, Kyushu University, 744 Motooka, Fukuoka 8190395 (Japan); Shimakawa, S.; Goto, M.; Nakagawa, S. [Japan Atomic Energy Agency, 4002 Oarai, Ibaraki (Japan); Nishikawa, M. [Malaysia-Japan International Institute of Technology, UTM, Kuala Lumpur 54100 (Malaysia)

    2014-05-01

    The performance of a high-temperature gas-cooled reactor as a tritium production device is examined, assuming the compound LiAlO{sub 2} as the tritium-producing material. A gas turbine high-temperature reactor of 300 MWe nominal capacity (GTHTR300) is assumed as the calculation target, and using the continuous-energy Monte Carlo transport code MVP-BURN, burn-up simulations are carried out. To load sufficient Li into the core, LiAlO{sub 2} is loaded into the removable reflectors that surround the ring-shaped fuel blocks in addition to the burnable poison insertion holes. It is shown that module high-temperature gas-cooled reactors with a total thermal output power of 3 GW can produce almost 8 kg of tritium in a year.

  5. Tritium handling facilities at the Los Alamos Scientific Laboratory

    International Nuclear Information System (INIS)

    Anderson, J.L.; Damiano, F.A.; Nasise, J.E.

    1975-01-01

    A new tritium facility, recently activated at the Los Alamos Scientific Laboratory, is described. The facility contains a large drybox, associated gas processing system, a facility for handling tritium gas at pressures to approximately 100 MPa, and an effluent treatment system which removes tritium from all effluents prior to their release to the atmosphere. The system and its various components are discussed in detail with special emphasis given to those aspects which significantly reduce personnel exposures and atmospheric releases. (auth)

  6. Dosimetry of skin-contact exposure to tritium gas contaminated surfaces

    International Nuclear Information System (INIS)

    Legare, M.

    1990-12-01

    The radiological hazards from tritium are usually associated with exposure to tritium oxide either by inhalation, ingestion or permeation through skin. However, exposure from skin contact with tritium gas contaminated surfaces represents a different radiological hazard in tritium removal facilities and future fusion power plants. Previous experiments on humans and more recent experiments on hairless rats at Chalk River Laboratories have shown that when a tritium gas-contaminated surface is brought into contact with intact skin, high concentrations of organically-bound tritium in urine and skin are observed which were not seen from single tritiated water (liquid or vapour form) contamination. The results of the rat experiments, which involved measurements of tritium activity in urine and skin, after contact with contaminated stainless steel, are described. These results are also compared to previous data from human experiments. The effect of various exposure conditions and different contaminated surfaces such as brass, aluminum and glass are analysed and related to the results from contaminated stainless steel exposure. Dosimetric models are being developed in order to improve the basis for dose assessment for this mode of tritium uptake. The presently studied model is explained along with the assumptions and methods involved in its derivation. The features of 'STELLA', the software program used to implement the model, are discussed. The methods used to estimate skin and whole body dose from a model are demonstrated. Finally, some experiments for improving the accuracy of the model are proposed. Briefly, this study compares the results from animal and human experiments as well as different exposure conditions, and determines the range of whole body and skin dose that may be involved from skin-contact intake. This information is essential for regulatory purposes particularly in the derivation of doses for skin-contact contamination. (15 figs., 7 tabs., 29 refs.)

  7. Exchange of moisture between atmosphere and ground regarding tritium transfer

    International Nuclear Information System (INIS)

    Bunnenberg, C.

    1980-09-01

    Two measuring equipment have been developed in the framework of this study which fulfill important conditions to avoid microclimatic interferences during measurement by using site-specific ground samples and embedding these in the ground surface. The beta-absorption lysimeter allows the detection of a minimum deposit height of 0.001 mm in a 1 mm sample layer. The conductivity moisture probe is to measure the moisture diffusion within the first 80 mm of the upper ground with a vertical spacial resolution of 2 mm. It is possible to measure a minimum water content increase of 0.02 wt% per 2 mm ground layer using this probe. The influences of single microclimatic parameter on condensation and evaporation were investigated and a transport equation was developed. Investigations in the Negev proved the application ability of the measuring equipment. The application of the transport equation showed very good agreement with the measured values. When the ground surface starts to cool in the afternoon, there is a countercurrent moisture transport from the atmosphere and the deeper ground layers which lead to a higher water content in the upper ground layer. At about 50 mm depth there is an overlapping layer of the two moisture flows which remains almost constant over the 24 h cycle. This exchange zone of atmospheric humidity and ground water must be paid great attention with regard to HTO transfer. (orig./HP) [de

  8. Gas-handling system for studies of tritium-containing materials

    International Nuclear Information System (INIS)

    Carstens, D.H.W.

    1975-01-01

    A gas handling system for preparation and study of tritium containing compounds and materials is described. The system at any one time can handle amounts of DT gas up to about 3 moles and has provisions for purification, storage, and measurement of the gas. Experimental conditions covering the ranges 20 to 800 0 C and 0.1 Pa to 137 MPa (10 -2 torr to 20,000 psi) can be maintained. (auth)

  9. Chromatographic measurement of hydrogen isotopic and permanent gas impurities in tritium

    International Nuclear Information System (INIS)

    Warner, D.K.; Kinard, C.; Bohl, D.C.

    1976-01-01

    This paper describes a gas chromatograph that was designed for dedicated analysis of hydrogen isotopic and permanent gas impurities in tritium and tritium-deuterium mixtures. The instrument that was developed substantially improved the accuracy and precision of hydrogen isotopic analysis in the 20 ppM to one mole percent range as compared with other analytical methods. Several unique design features of the instrument were required due to the radiation and isotopic exchange properties of the tritium in the samples; descriptions of these features are presented along with details of the complete chromatographic system. The experimental procedures used to calibrate the detector and statistically evaluate its performance are given, and the sources of analytical error are cited. The limitations of the present system are also discussed

  10. Gas separation performance of a hollow-filament type polyimide membrane module for a compact tritium removal system

    International Nuclear Information System (INIS)

    Hayashi, Takumi; Yamada, Masayuki; Suzuki, Takumi; Matsuda, Yuji; Okuno, Kenji

    1995-01-01

    A new tritium removal system using gas separation membranes has been studied to develop more compact and cost-effective system for a fusion reactor. To obtain necessary parameters, which are directly scalable to the ITER Atmospheric Detritiation System, the basic tritium recovery performance was investigated with a scaled polyimide membrane module (hollow-filament type : 10 m 3 /hr) loop. The result shows that the H 2 recovery ratio from N 2 or air was more than 99% or about 97%, respectively, at flow rate ratio of permeated/feed = 0.1, feed ampersand permeated side pressures = 2580 ampersand 80 torr, and module temp. = 293 K. Tritium (HT) recovery function was almost the same as H 2 recovery, even though the total hydrogen concentration was a few ppm in the feed of module. H 2 O recovery performance was better than hydrogen recovery. These recovery functions were improved effectively decreasing the pressure ratio of permeated/feed of module. 5 refs., 11 figs

  11. Influence of additives and impurities in sweep gas and solid tritium release behaviour from lithium ceramics (review)

    International Nuclear Information System (INIS)

    Tanaka, Satoru

    1991-01-01

    Tritium release from solid breeding material is affected by small amounts of additives or impurities in the sweep gas or solid itself. Addition of hydrogen or water vapor to the sweep gas is reported to enhance the surface reaction of tritium release. Doping to solid breeder with elements of different valence from lithium has a possibility to improve tritium diffusion in the solid. Surface reaction and migration behavior in bulk are believed to be also affected by impurities in the sweep gas and in the solid. In order to model tritium release behavior in the blanket of fusion reactor, the mechanism of interaction with these additives or impurities must be quantitatively formulated. However, the mechanism of these remains to be elucidated. In this paper effects of these additives and impurities on tritium migration are reviewed. The mechanism of surface reaction for He+H 2 sweep gas is also discussed. (orig.)

  12. Tritium assay in hydrogen gas by proportional counter with magnetic tape recording

    International Nuclear Information System (INIS)

    Grabczak, J.

    1982-03-01

    Analytical procedure is discussed concerning routine tritium activity determination in water samples based on hydrogen production from the water sample and radioactivity measurement by gas proportional counting. The method was found to be fully comparable to the widely adopted technique of liquid scintillation counting with electrolytic enrichment

  13. Suppression of Tritium Retention in Remote Areas of ITER by Nonperturbative Reactive Gas Injection

    NARCIS (Netherlands)

    Tabares, F. L.; Ferreira, J. A.; Ramos, A.; van Rooij, G. J.; Westerhout, J.; Al, R.; Rapp, J.; Drenik, A.; Mozetic, M.

    2010-01-01

    A technique based on reactive gas injection in the afterglow region of the divertor plasma is proposed for the suppression of tritium-carbon codeposits in remote areas of ITER when operated with carbon-based divertor targets. Experiments in a divertor simulator plasma device indicate that a 4 nm/min

  14. Techniques for tritium recovery from carbon flakes and dust at the JET active gas handling system

    International Nuclear Information System (INIS)

    Gruenhagen, S.; Perevezentsev, A.; Brennan, P. D.; Camp, P.; Knipe, S.; Miller, A.; Yorkshades, J.

    2008-01-01

    Detritiation of highly tritium contaminated carbon and metal material used as first wall armour is a key issue for fusion machines like JET and ITER. Re-deposited carbon and hydrogen in the form of flakes and dust can lead to a build-up of the tritium inventory and therefore this material must be removed and processed. The high tritium concentration of the flake and dust material collected from the JET vacuum vessel makes it unsuitable for direct waste disposal without detritiation. A dedicated facility to process the tritiated carbon flake material and recover the tritium has been designed and built. In several test runs active material was successfully processed and de-tritiated in the new facility. Samples containing only carbon and hydrogen isotopes have been completely oxidized without any residue. Samples containing metallic impurities, e.g. beryllium, require longer processing times, adjusted processing parameters and yield an oxide residue. The detritiation factor was 2x10 4 . In order to simulate in-vessel and ex-vessel detritiation techniques, the detritiation of a carbon flake sample by isotopic exchange in a hydrogen atmosphere was investigated. 2.8% of tritium was recovered by this means. (authors)

  15. Tritium conference days; Journees tritium

    Energy Technology Data Exchange (ETDEWEB)

    Garnier-Laplace, J.; Lebaron-Jacobs, L.; Sene, M.; Devin, P.; Chretien, V.; Le Guen, B.; Guetat, Ph.; Baglan, N.; Ansoborlo, E.; Boyer, C.; Masson, M.; Bailly-Du-Bois, P.; Jenkinson, St.; Wakeford, R.; Saintigny, Y.; Romeo, P.H.; Thompson, P.; Leterq, D.; Chastagner, F.; Cortes, P.; Philippe, M.; Paquet, F.; Fournier, M.

    2009-07-01

    This document gathers the slides of the available presentations given during this conference day. Twenty presentations out of 21 are assembled in the document and deal with: 1 - tritium in the environment (J. Garnier-Laplace); 2 - status of knowledge about tritium impact on health (L. Lebaron-Jacobs); 3 - tritium, discrete but present everywhere (M. Sene); 4 - management of tritium effluents from Areva NC La Hague site - related impact and monitoring (P. Devin); 5 - tritium effluents and impact in the vicinity of EDF's power plants (V. Chretien and B. Le Guen); 6 - contribution of CEA-Valduc centre monitoring to the knowledge of atmospheric tritiated water transfers to the different compartments of the environment (P. Guetat); 7 - tritium analysis in environment samples: constraints and means (N. Baglan); 8 - organically-linked tritium: the analyst view (E. Ansoborlo); 9 - study of tritium transfers to plants via OBT/HTO{sub air} and OBT/HTO{sub free} (C. Boyer); 10 - tritium in the British Channel (M. Masson and P. Bailly-Du-Bois); 11 - tritium in British coastal waters (S. Jenkinson); 12 - recent results from epidemiology (R. Wakeford); 13 - effects of tritiated thymidine on hematopoietic stem cells (P.H. Romeo); 14 - tritium management issue in Canada: the point of view from authorities (P. Thompson); 15 - experience feedback of the detritiation process of Valduc centre (D. Leterq); 16 - difficulties linked with tritiated wastes confinement (F. Chastagner); 17 - optimisation of tritium management in the ITER project (P. Cortes); 18 - elements of thought about the management of tritium generated by nuclear facilities (M. Philippe); 19 - CIPR's position about the calculation of doses and risks linked with tritium exposure (F. Paquet); 20 - tritium think tanks (M. Fournier). (J.S.)

  16. Mesoscale atmospheric modeling of the July 12, 1992 tritium release from the Savannah River Site

    International Nuclear Information System (INIS)

    Fast, J.D.; O'Steen, B.L.; Addis, R.P.

    1992-01-01

    In August of 1991, the Environmental Transport Group (ETG) began the development of an advanced Emergency Response (ER) system based upon the Colorado State University Regional Atmospheric Modeling System (RAMS). This model simulates the three-dimensional, time-dependent, flow field and thermodynamic structure of the planetary boundary layer (PBL). A companion Lagrangian Particle Dispersion Model (LPDM) simulates contaminant transport based on the flow and turbulence fields generated by RAMS. This paper describes the performance of the advanced ER system in predicting transport and diffusion near the SRS when compared to meteorological and sampling data taken during the July 12, 1992 tritium release. Since PUFF/PLUME and 2DPUF are two Weather INformation and Display (WIND) System atmospheric models that were used to predict the transport and diffusion of the plume at the time of the release, the results from the advanced ER system are also compared to those produced by PUFF/PLUME and 2DPUF

  17. Deuterium migration in nuclear graphite: consequences for the behavior of tritium in Gas Cooled Reactors and for the decontamination of irradiated graphite waste

    International Nuclear Information System (INIS)

    Le-Guillou, Mael

    2014-01-01

    In France, 23 000 t of irradiated graphite that will be generated by the decommissioning of the first generation Uranium Naturel-Graphite-Gaz (UNGG) nuclear reactors are waiting for a long term management solution. This work focuses on the behavior of tritium, which is one of the main contributors to the radiological inventory of graphite waste after reactor shutdown. In order to anticipate tritium release during dismantling or waste management, it is mandatory to collect data on its migration, location and inventory. Our study is based on the simulation of tritium by implantation of approximately 3 at. % of deuterium up to around 3 μm in a virgin nuclear graphite. This material was then annealed up to 300 h and 1300 C in inert atmosphere, UNGG coolant gas and humid gas, aiming to reproduce thermal conditions close to those encountered in reactor and during waste management operations. The deuterium profiles and spatial distribution were analyzed using the nuclear reaction 2 H( 3 He,p) 4 He. The main results evidence a thermal release of implanted deuterium occurring essentially through three regimes controlled by the detrapping of atomic deuterium located in superficial or interstitial sites. The extrapolation of our data to tritium suggests that its purely thermal release during reactor operations may have been lower than 30 % and would be located close to the graphite free surfaces. Consequently, most of the tritium inventory after reactor shutdown could be trapped deeply within the irradiated graphite structure. Decontamination of graphite waste should then require temperatures higher than 1300 C, and would be more efficient in dry inert gas than in humid gas. (author)

  18. Tritium trick

    Science.gov (United States)

    Green, W. V.; Zukas, E. G.; Eash, D. T.

    1971-01-01

    Large controlled amounts of helium in uniform concentration in thick samples can be obtained through the radioactive decay of dissolved tritium gas to He3. The term, tritium trick, applies to the case when helium, added by this method, is used to simulate (n,alpha) production of helium in simulated hard flux radiation damage studies.

  19. Gas fired boilers and atmospheric pollution

    International Nuclear Information System (INIS)

    Chiaranello, J.M.

    1991-01-01

    A general analysis concerning atmospheric pollution is presented: chemical composition and vertical distribution of atmosphere and pollutants, chemical reactions, ozone destruction and production cycles, COx, NOx and SOx pollutions. The gas fired boiler number and repartition in France are presented and the associated pollution is analyzed (CO2, CO, NOx) and quantified. Various pollution control technics concerning gas fired boiler pollutants are described and a pollution criterion for clean gas fired generators is proposed

  20. Diffusion of gases in solids: rare gas diffusion in solids; tritium diffusion in fission and fusion reactor metals. Final report

    International Nuclear Information System (INIS)

    Abraham, P.M.; Chandra, D.; Mintz, J.M.; Elleman, T.S.; Verghese, K.

    1976-01-01

    Major results of tritium and rare gas diffusion research conducted under the contract are summarized. The materials studied were austenitic stainless steels, Zircaloy, and niobium. In all three of the metal systems investigated, tritium release rates were found to be inhibited by surface oxide films. The effective diffusion coefficients that control tritium release from surface films on Zircaloy and niobium were determined to be eight to ten orders of magnitude lower than the bulk diffusion coefficients. A rapid component of diffusion due to grain boundaries was identified in stainless steels. The grain boundary diffusion coefficient was determined to be about six orders of magnitude greater than the bulk diffusion coefficient for tritium in stainless steel. In Zircaloy clad fuel pins, the permeation rate of tritium through the cladding is rate-limited by the extremely slow diffusion rate in the surface films. Tritium diffusion rates through surface oxide films on niobium appear to be controlled by cracks in the surface films at temperatures up to 600 0 C. Beyond 600 0 C, the cracks appear to heal, thereby increasing the activation energy for diffusion through the oxide film. The steady-state diffusion of tritium in a fusion reactor blanket has been evaluated in order to calculate the equilibrium tritium transport rate, approximate time to equilibrium, and tritium inventory in various regions of the reactor blanket as a function of selected blanket parameters. Values for these quantities have been tabulated

  1. Purification of inert gas circuits of nuclear power facilities from tritium and hydrogen

    International Nuclear Information System (INIS)

    Eichler, R.

    1985-08-01

    Removing hydrogen and tritium from the inert primary coolant of a high temperature reactor is very important in regard to the process heat disposition. In this work a gas purification for a high temperature module reactor was laid out constructionally and researched technically. This system removes the contamination of the primary circuit with the aid of chemical getter beds of Cer alloy particles. (orig./PW) [de

  2. Detection of tritium in the CO{sub 2} of the reactors G2/G3 using gas chromatography; La detection du tritium par chromatographie gazeuse dans le CO{sub 2} des piles G2/G3

    Energy Technology Data Exchange (ETDEWEB)

    Guillermin, P; Rossi, J [Commissariat a l' Energie Atomique, Saclay (France). Centre d' Etudes Nucleaires

    1965-07-01

    This gas-phase chromatographic method, based on the principle of the decomposition of a gas mixture into its pure constituents, makes it possible to identify and rapidly measure the tritium present in the heat-carrying fluid of the reactors G2/G3. The sensitivity limit corresponds to 5 x 10{sup -6} {mu}Ci/cm{sup 3} of tritiated gas, whereas the threshold reading of the D.C.C.A. is 10{sup -3} {mu}Ci/cm{sup 3} in the presence of {sup 41}A. This apparatus has interesting applications in the conditions where certain {beta} emitters (products of fission or of activation) interfere with the measurement of the tritium. It can easily be adapted to the detection of tritiated steam on condition that a reducing chemical treatment is applied for the atmospheric humidity. In fact, although this method is not as sensitive for the measurement of tritiated vapour as p-spectrometry in a scintillating medium, it may be set up very easily for measuring the C.M.A of tritium in air and is not affected by the presence of radio-active gases. (authors) [French] Cette methode de chromatographie en phase gazeuse, basee sur le principe de decomposition d'un melange gazeux en ses constituants purs, permet l'identification et la mesure rapide du tritium present dans le fluide caloporteur des piles G2/G3. La limite de sensibilite correspond a 5.10{sup -6} {mu}Ci/cm{sup 3} de gaz tritie, alors que le seuil de lecture du D.C.C.A. s'eleve a 10{sup -3} {mu}Ci/cm{sup 3} en presence de {sup 41}A. Cet appareillage presente un champ d'application interessant dans les domaines ou certains emetteurs {beta} (produits de fission ou d'activation) genent la mesure du tritium. Il peut s'adapter sans difficulte a la detection de la vapeur tritiee moyennant un traitement chimique reducteur de l'humidite atmospherique. En definitive, bien que cette methode ne soit pas aussi sensible pour la determination de la vapeur tritiee que la spectrometrie {beta} en milieu scintillant, elle permet de mesurer la C.M.A de

  3. Variation of atmospheric tritium concentration in three chemical forms at Toki, Japan: 2004-12.

    Science.gov (United States)

    Tanaka, M; Uda, T

    2015-11-01

    Atmospheric tritium concentrations of HTO, HT and CH3T have been measured at Toki, Japan, for the environmental impact assessment of tritium for a fusion test facility. According to the data from 2004 to 2012, the concentrations of HT and HTO in water vapour tend to increase in spring. The seasonal variation in HT concentration at Toki was compared with the H2 concentration between 1990 and 2005 at Tae-ahn Peninsula, Republic of Korea, which is at approximately the same latitude as Toki. The monthly average of HT-specific activity varied from 1.24 × 10(5) to 1.76 × 10(5) TU. The peak of the monthly average H2 concentration did not match that of HT. This indicates that the mechanism of the production or the source of HT might be different from the production mechanism of H2. © The Author 2015. Published by Oxford University Press. All rights reserved. For Permissions, please email: journals.permissions@oup.com.

  4. Tritium processing in JT-60U

    International Nuclear Information System (INIS)

    Miya, Naoyuki; Masaki, Kei

    1997-01-01

    Tritium retention analysis and tritium concentration measurement have been made during the large Tokamak JT-60U deuterium operations. This work has been carried out to evaluate the tritium retention for graphite tiles inside the vacuum vessel and tritium release characteristics in the tritium cleanup operations. JT-60U has carried out D-D experiments since July 1991. In the deuterium operations during the first two years, about 1.7 x 10 19 D-D fusion neutrons were produced by D (d, p) T reactions in plasma, which are expected to produce ∼31 GBq of tritium. The tritium produced is evacuated by a pumping system. A part of tritium is, however, trapped in the graphite tiles. Several sample tiles were removed from the vessel and the retained tritium Distribution in the tiles was measured using a liquid scintillator. The results of poloidal distribution showed that the tritium concentration in the divertor tiles was higher than that in the first wall tiles and it peaked in the tiles between two strike points of divertor magnetic lines. Tritium concentration in the exhaust gas from the vessel have also been measured with an ion chamber during the tritium cleanup operations with hydrogen divertor discharges and He-GDC. Total of recovered tritium during the cleanup operations was ∼ 7% of that generated. The results of these measurements showed that the tritium of 16-23 GBq still remained in the graphite tiles, which corresponded to about 50-70% of the tritium generated in plasma. The vessel is ventilated during the in-vessel maintenance works, then the atmosphere is always kept lower than the legal concentration guide level of 0.7 Bq/cm 3 for radiation work permit requirements. (author)

  5. Oxidation of atmospheric molecular tritium in plant leaves, lichens and mosses

    Energy Technology Data Exchange (ETDEWEB)

    Ichimasa, Michiko; Ichimasa, Yusuke; Yagi, Yoshimi; Ko, Rinkei [Ibaraki Univ., Mito (Japan). Faculty of Science; Suzuki, Masatomo; Akita, Yasukazu

    1989-12-01

    The oxidation of atmospheric molecular tritium (HT) in vegetation was determined by in vitro experiments for pine needles, pine bark, lichens attached to pine trees, taken from a coastal pine forest in Ibaraki prefecture and comparison of such measurements was made with those in soil. The oxidation of HT in pine needles was extremely low, being only about 1/40000 that in the surface soil of a pine forest, whereas its oxidation in pine bark with a lichen was almost 1000-7000 times higher than that in pine needles. HT oxidation in pine bark, a lichen and a moss was determined in each case under light and dark conditions and was found to be essentially the same. All mosses and lichens examined in the present study were found to have unusually high levels of HT oxidation whether their habitat was tree or ground surface. (author).

  6. Review of tritium confinement and atmosphere detritiation system in hot cells complex

    International Nuclear Information System (INIS)

    Rizzello, Claudio; Borgognoni, Fabio; Pinna, Tonio; Tosti, Silvano

    2010-01-01

    The tritium confinement strategy adopted during the past years in the ITER hot cell building is compared to the safety requirements given by the standard ISO-17873 'Nuclear facilities - criteria for the design and operation of ventilation systems for nuclear installations other than nuclear reactors'. In fact, this is the reference safety guideline recommended by French licensing authorities. Several features of the considered design of the hot cell building are not in agreement with these guidelines. Main discrepancies concern the zoning of the hot cell complex, the flow rates of ventilation, and the possibility to recycle the room atmosphere and to detritiate the effluent air. These aspects are discussed together with some proposed modifications of the design.

  7. Oxidation of atmospheric molecular tritium in plant leaves, lichens and mosses

    International Nuclear Information System (INIS)

    Ichimasa, Michiko; Ichimasa, Yusuke; Yagi, Yoshimi; Ko, Rinkei; Suzuki, Masatomo; Akita, Yasukazu.

    1989-01-01

    The oxidation of atmospheric molecular tritium (HT) in vegetation was determined by in vitro experiments for pine needles, pine bark, lichens attached to pine trees, taken from a coastal pine forest in Ibaraki prefecture and comparison of such measurements was made with those in soil. The oxidation of HT in pine needles was extremely low, being only about 1/40000 that in the surface soil of a pine forest, whereas its oxidation in pine bark with a lichen was almost 1000-7000 times higher than that in pine needles. HT oxidation in pine bark, a lichen and a moss was determined in each case under light and dark conditions and was found to be essentially the same. All mosses and lichens examined in the present study were found to have unusually high levels of HT oxidation whether their habitat was tree or ground surface. (author)

  8. Evaporational losses under different soil moisture regimes and atmospheric evaporativities using tritium

    International Nuclear Information System (INIS)

    Saxena, P.; Chaudhary, T.N.; Mookerji, P.

    1991-01-01

    Tritium as tracer was used in a laboratory study to estimate the contribution of moisture from different soil depths towards actual soil water evaporation. Results indicated that for comparable amounts of free water evaporation (5 cm), contribution of moisture from 70-80 cm soil layer towards total soil moisture loss through evaporation increased nearly 1.5 to 3 folds for soils with water table at 90 cm than without water table. Identical initial soil moistures were exposed to different atmospheric evaporativities. Similarly, for a given initial soil moisture status, upward movement of moisture from 70-80 cm soil layer under low evaporativity was nearly 8 to 12 times that of under high evaporativity at 5 cm free water evaporation value. (author). 6 refs., 4 tabs., 2 figs

  9. A study of wet deposition of atmospheric tritium releases at the Ontario Power Generation, Pickering Nuclear Generating Station

    International Nuclear Information System (INIS)

    Crooks, G.; DeWilde, J.; Yu, L.

    2001-01-01

    The Ontario Power Generation,Pickering Nuclear Generating Station (PNGS) has been investigating deposition of atmospheric releases of tritium on their site. This study has included numerical dispersion modelling studies conducted over the past three years, as well as an ongoing field monitoring study. The following paper will present results of the field monitoring study and make comparisons to the numerical modelling. The results of this study could be of potential use to nuclear stations in quantifying tritium deposition in near field regions where building wake effects dominate pollutant dispersion

  10. Tritium concentrations in the atmospheric environment at Rokkasho, Japan before the final testing of the spent nuclear fuel reprocessing plant

    International Nuclear Information System (INIS)

    Akata, Naofumi; Kakiuchi, Hideki; Shima, Nagayoshi; Iyogi, Takashi; Momoshima, Noriyuki; Hisamatsu, Shun'ichi

    2011-01-01

    This study aimed at obtaining background tritium concentrations in precipitation and air at Rokkasho where the first commercial spent nuclear fuel reprocessing plant in Japan has been under construction. Tritium concentration in monthly precipitation during fiscal years 2001-2005 had a seasonal variation pattern which was high in spring and low in summer. The tritium concentration was higher than that observed at Chiba City as a whole. The seasonal peak concentration at Rokkasho was generally higher than that at Chiba City, while the baseline concentrations of both were similar. The reason for the difference may be the effect of air mass from the Asian continent which is considered to have high tritium concentration. Atmospheric tritium was operationally separated into HTO, HT and hydrocarbon (CH 3 T) fractions, and the samples collected every 3 d-14 d during fiscal year 2005 were analyzed for these fractions. The HTO concentration as radioactivity in water correlated well with that in the precipitation samples. The HT concentration was the highest among the chemical forms analyzed, followed by the HTO and CH 3 T concentrations. The HT and CH 3 T concentrations did not have clear seasonal variation patterns. The HT concentration followed the decline previously reported by Mason and Ostlund with an apparent half-life of 4.8 y. The apparent and environmental half-lives of CH 3 T were estimated as 9.2 y and 36.5 y, respectively, by combining the present data with literature data. The Intergovernmental Panel on Climate Change used the atmospheric lifetime of 12 y for CH 4 to estimate global warming in its 2007 report. The longer environmental half-life of CH 3 T suggested its supply from other sources than past nuclear weapon testing in the atmosphere. - Highlights: → We observed background tritium concentrations in atmospheric environment at Rokkasho, Japan. → Tritium concentration in precipitation was high in spring and low in summer. → The atmospheric HT

  11. Tritium concentrations in the atmospheric environment at Rokkasho, Japan before the final testing of the spent nuclear fuel reprocessing plant

    Energy Technology Data Exchange (ETDEWEB)

    Akata, Naofumi, E-mail: nao@ies.or.jp [Department of Radioecology, Institute for Environmental Sciences, 1-7 Ienomae, Obuchi, Rokkasho, Aomori 039-3212 (Japan); Kakiuchi, Hideki [Department of Radioecology, Institute for Environmental Sciences, 1-7 Ienomae, Obuchi, Rokkasho, Aomori 039-3212 (Japan); Shima, Nagayoshi [Entex Inc., 1-2-8 Asahi, Kashiwa, Chiba 277-0852 (Japan); Iyogi, Takashi [Department of Radioecology, Institute for Environmental Sciences, 1-7 Ienomae, Obuchi, Rokkasho, Aomori 039-3212 (Japan); Momoshima, Noriyuki [Radioisotope Center, Kyushu University, 6-10-1 Hakozaki, Higashi-ku, Fukuoka 812-8581 (Japan); Hisamatsu, Shun' ichi [Department of Radioecology, Institute for Environmental Sciences, 1-7 Ienomae, Obuchi, Rokkasho, Aomori 039-3212 (Japan)

    2011-09-15

    This study aimed at obtaining background tritium concentrations in precipitation and air at Rokkasho where the first commercial spent nuclear fuel reprocessing plant in Japan has been under construction. Tritium concentration in monthly precipitation during fiscal years 2001-2005 had a seasonal variation pattern which was high in spring and low in summer. The tritium concentration was higher than that observed at Chiba City as a whole. The seasonal peak concentration at Rokkasho was generally higher than that at Chiba City, while the baseline concentrations of both were similar. The reason for the difference may be the effect of air mass from the Asian continent which is considered to have high tritium concentration. Atmospheric tritium was operationally separated into HTO, HT and hydrocarbon (CH{sub 3}T) fractions, and the samples collected every 3 d-14 d during fiscal year 2005 were analyzed for these fractions. The HTO concentration as radioactivity in water correlated well with that in the precipitation samples. The HT concentration was the highest among the chemical forms analyzed, followed by the HTO and CH{sub 3}T concentrations. The HT and CH{sub 3}T concentrations did not have clear seasonal variation patterns. The HT concentration followed the decline previously reported by Mason and Ostlund with an apparent half-life of 4.8 y. The apparent and environmental half-lives of CH{sub 3}T were estimated as 9.2 y and 36.5 y, respectively, by combining the present data with literature data. The Intergovernmental Panel on Climate Change used the atmospheric lifetime of 12 y for CH{sub 4} to estimate global warming in its 2007 report. The longer environmental half-life of CH{sub 3}T suggested its supply from other sources than past nuclear weapon testing in the atmosphere. - Highlights: > We observed background tritium concentrations in atmospheric environment at Rokkasho, Japan. > Tritium concentration in precipitation was high in spring and low in summer. > The

  12. Levels of tritium in soils and vegetation near Canadian nuclear facilities releasing tritium to the atmosphere: implications for environmental models.

    Science.gov (United States)

    Thompson, P A; Kwamena, N-O A; Ilin, M; Wilk, M; Clark, I D

    2015-02-01

    Concentrations of organically bound tritium (OBT) and tritiated water (HTO) were measured over two growing seasons in vegetation and soil samples obtained in the vicinity of four nuclear facilities and two background locations in Canada. At the background locations, with few exceptions, OBT concentrations were higher than HTO concentrations: OBT/HTO ratios in vegetation varied between 0.3 and 20 and values in soil varied between 2.7 and 15. In the vicinity of the four nuclear facilities OBT/HTO ratios in vegetation and soils deviated from the expected mean value of 0.7, which is used as a default value in environmental transfer models. Ratios of the OBT activity concentration in plants ([OBT]plant) to the OBT activity concentration in soils ([OBT]soil) appear to be a good indicator of the long-term behaviour of tritium in soil and vegetation. In general, OBT activity concentrations in soils were nearly equal to OBT activity concentrations in plants in the vicinity of the two nuclear power plants. [OBT]plant/[OBT]soil ratios considerably below unity observed at one nuclear processing facility represents historically higher levels of tritium in the environment. The results of our study reflect the dynamic nature of HTO retention and OBT formation in vegetation and soil during the growing season. Our data support the mounting evidence suggesting that some parameters used in environmental transfer models approved for regulatory assessments should be revisited to better account for the behavior of HTO and OBT in the environment and to ensure that modelled estimates (e.g., plant OBT) are appropriately conservative. Crown Copyright © 2014. Published by Elsevier Ltd. All rights reserved.

  13. Tritium concentrations in the atmospheric environment at Rokkasho, Japan before the final testing of the spent nuclear fuel reprocessing plant.

    Science.gov (United States)

    Akata, Naofumi; Kakiuchi, Hideki; Shima, Nagayoshi; Iyogi, Takashi; Momoshima, Noriyuki; Hisamatsu, Shun'ichi

    2011-09-01

    This study aimed at obtaining background tritium concentrations in precipitation and air at Rokkasho where the first commercial spent nuclear fuel reprocessing plant in Japan has been under construction. Tritium concentration in monthly precipitation during fiscal years 2001-2005 had a seasonal variation pattern which was high in spring and low in summer. The tritium concentration was higher than that observed at Chiba City as a whole. The seasonal peak concentration at Rokkasho was generally higher than that at Chiba City, while the baseline concentrations of both were similar. The reason for the difference may be the effect of air mass from the Asian continent which is considered to have high tritium concentration. Atmospheric tritium was operationally separated into HTO, HT and hydrocarbon (CH(3)T) fractions, and the samples collected every 3 d-14 d during fiscal year 2005 were analyzed for these fractions. The HTO concentration as radioactivity in water correlated well with that in the precipitation samples. The HT concentration was the highest among the chemical forms analyzed, followed by the HTO and CH(3)T concentrations. The HT and CH(3)T concentrations did not have clear seasonal variation patterns. The HT concentration followed the decline previously reported by Mason and Östlund with an apparent half-life of 4.8 y. The apparent and environmental half-lives of CH(3)T were estimated as 9.2 y and 36.5 y, respectively, by combining the present data with literature data. The Intergovernmental Panel on Climate Change used the atmospheric lifetime of 12 y for CH(4) to estimate global warming in its 2007 report. The longer environmental half-life of CH(3)T suggested its supply from other sources than past nuclear weapon testing in the atmosphere. Copyright © 2011 Elsevier Ltd. All rights reserved.

  14. Improvement of organic compounds labelling method with the use of thermally activated tritium gas

    International Nuclear Information System (INIS)

    Nejman, L.A.; Smolyakov, V.S.; Antropova, L.P.

    1982-01-01

    Use of a support (various types of papers) is recommended for organic compounds labelling by tritium gas activated at a hot tungsten filament. This improvement increases chemical and radiochemical yields and makes the experiment simpler and faster. Generally labelled triethyloxonium tetra-fluoroborate, ethyl-p-aminobenzoate, p-aminobenzoic acid (Na-salt), A-factor (a natural regulator of streptomycin biosynthesis), decapeptide angiotensin I, phospholipid 1, 2 - dimyristoyl-sn-glycero-3--phosphocholine and E. coli tRNAs have been prepared by this method. Molar radioactivity of the labelled compounds is in the range of 1-200 GBg/mmole [ru

  15. Production of ultrapure D-T gas by removal of molecular tritium by selective adsorption

    International Nuclear Information System (INIS)

    Maienschein, J.L.; Hudson, R.S.; Tsugawa, R.T.; Fearon, E.M.; Souers, P.C.; Collins, G.W.

    1991-07-01

    The application of selective adsorption to purification of D-T gas by removal of T 2 has been demonstrated for small quantities of gas typical in research applications. This represents a variation on the production of pure spin isomers of deuterium and hydrogen. The use of an adsorption column offers several advantages over conventional separation techniques, such as low tritium inventory, rapid delivery to prevent radiation damage of the accumulated product, compact size, simplicity of design, construction, and operation, and operation without carrier gas. Because a column can have several thousand equilibrium stages, the purity of the product can be very high. The adsorption column has been shown to be an attractive separation tool for small quantities of hydrogen isotopes

  16. Tritium surface loading due to contamination of rainwater from atmospheric release at NAPS

    International Nuclear Information System (INIS)

    Sharma, L.N.; Dube, B.; Varakhedkar, V.K.

    2001-01-01

    Annual tritium (HTO) surface loading has been measured and calculated for the year 1998-99 within 0.8 km distance from 145m high stack of Narora Atomic Power Station (NAPS) at eight locations in different directions. The technique for measured values consists of the summation of product of tritium concentration (Bq/l) in daily rainfall samples and daily rainfall (mm) whereas that for calculated values having the use of prevailing meteorological conditions and average tritium release rate during a year. The ratios of measured and calculated values of tritium surface loading during the years 1998-99 are found to be in the range of 0.18 to 6.97. Tritium surface loading studies at NAPS reveal that a fraction 1.7E-03 of total annual tritium released through stack gets deposited on the surface due to washout / rainout of plume within 0.8 km radial distance from stack. The range of deposition velocity, V w (m.s - 1 ) i.e the ratio of annual tritium surface loading W(Bq.m - 2 . s - 1 ) and annual mean tritium concentration in air, χo(Bq.m - 3) at three locations for the years 1998-99 is found to be 5.59E-04 to 5.99E-03 ms - 1 . The average value for wet deposition velocity V bar w for NAPS site is estimated as 2.92E-03 m.s - 1. (author)

  17. Factors affecting calculations of dose resulting from a tritium release into the atmosphere

    International Nuclear Information System (INIS)

    Otaduy, P.; Easterly, C.E.; Booth, R.S.; Jacobs, D.G.

    1976-01-01

    Tritium releases in the form of HT represent a lower hazard to man than releases as HTO. However, during movement in the environment, HT is converted into HTO. The effects of the conversion rate on calcultions of dose are described, and a general method is presented for determining the dose from tritium for various conversion rates and relative HTO/HT risk factors

  18. Atmospheric tritium. Progress report, 1 April 1976--30 June 1977

    International Nuclear Information System (INIS)

    Ostlund, H.G.

    1977-01-01

    Data are reported from regular, twice or three times weekly, sampling of atmospheric HTO and HT at stations in Miami, FL; Mauna Loa, HI; Fairbanks, AK; and Baring Head, N.Z. In addition, sampling has begun in Miami also for tritium bound in lower hydrocarbons, here called CH 3 T. In December 1974--January 1975, and again in January--February 1976, sampling was performed on board a ship en route from California to McMurdo (Antarctic). The data show a gentle, slight dilution of HT southwards from about 52 at/mg at 36 0 N to about 40 at/mg in New Zealand and south. During the period of this Data Report, the laboratory also participated in Project Airstream. Five series of stratospheric sampling flights were made, the programmed area of coverage of each was from 10 0 S latitude to 75 0 N latitude, and altitudes between 12 km and 19 km. The data are not included in this report, but will be published at an early date. In cooperation with the International Atomic Energy Agency (IAEA)/World Meteorological Organization Isotopes-in-Precipitation Network, monthly composite rain samples were measured for Miami, Barbados, and Western Samoa

  19. Large-scale distribution of tritium in a commercial product

    International Nuclear Information System (INIS)

    Combs, F.; Doda, R.J.

    1979-01-01

    Tritium enters the environment from various sources including nuclear reactor operations, weapons testing, natural production, and from the manufacture, use and ultimate disposal of commercial products containing tritium. A recent commercial application of tritium in the United States of America involves the backlighting of liquid crystal displays (LCD) in digital electronic watches. These watches are distributed through normal commercial channels to the general public. One million curies (MCi) of tritium were distributed in 1977 in this product. This is a significant quantity of tritium compared with power reactor-produced tritium (3MCi yearly) or with naturally produced tritium (6MCi yearly). This is the single largest commercial application involving tritium to date. The final disposition of tritium from large quantities of this product, after its useful life, must be estimated by considering the means of disposal and the possibility of dispersal of tritium concurrent with disposal. The most likely method of final disposition of this product will be disposal in solid refuse; this includes burial in land fills and incineration. Burial in land fills will probably contain the tritium for its effective lifetime, whereas incineration will release all the tritium gas (as the oxide) to the atmosphere. The use and disposal of this product will be studied as part of an environmental study that is at present being prepared for the U.S. Nuclear Regulatory Commission. (author)

  20. Mars Atmospheric Capture and Gas Separation

    Science.gov (United States)

    Muscatello, Anthony; Santiago-Maldonado, Edgardo; Gibson, Tracy; Devor, Robert; Captain, James

    2011-01-01

    The Mars atmospheric capture and gas separation project is selecting, developing, and demonstrating techniques to capture and purify Martian atmospheric gases for their utilization for the production of hydrocarbons, oxygen, and water in ISRU systems. Trace gases will be required to be separated from Martian atmospheric gases to provide pure C02 to processing elements. In addition, other Martian gases, such as nitrogen and argon, occur in concentrations high enough to be useful as buffer gas and should be captured as welL To achieve these goals, highly efficient gas separation processes will be required. These gas separation techniques are also required across various areas within the ISRU project to support various consumable production processes. The development of innovative gas separation techniques will evaluate the current state-of-the-art for the gas separation required, with the objective to demonstrate and develop light-weight, low-power methods for gas separation. Gas separation requirements include, but are not limited to the selective separation of: (1) methane and water from un-reacted carbon oxides (C02- CO) and hydrogen typical of a Sabatier-type process, (2) carbon oxides and water from unreacted hydrogen from a Reverse Water-Gas Shift process, (3) carbon oxides from oxygen from a trash/waste processing reaction, and (4) helium from hydrogen or oxygen from a propellant scavenging process. Potential technologies for the separations include freezers, selective membranes, selective solvents, polymeric sorbents, zeolites, and new technologies. This paper and presentation will summarize the results of an extensive literature review and laboratory evaluations of candidate technologies for the capture and separation of C02 and other relevant gases.

  1. Tritium surface loading due to contamination of rainwater from atmospheric release at NAPS (2011)

    International Nuclear Information System (INIS)

    Gautam, Y.P.; Sharma, Saivajay; Rao, K.S.; Singh, Bhikam; Kumar, Avinash; Ravi, P.M.

    2012-01-01

    Annual tritium (HTO) surface loading has been measured and calculated for the year 2011 within 0.8 km distance from 145 m high stack of Narora Atomic Power Station (NAPS) at eight locations in different directions. The technique for measured values consists of the summation of product of tritium concentration (Bq/l) in daily rainfall samples and daily rainfall (mm). Tritium surface loading studies at NAPS reveal that a fraction 1.01E-03 of total annual tritium released through stack gets deposited on the surface due to washout/rainout of plume within 0.8 km radial distance from stack. The range of deposition velocity, Vw (m.s -1 ) i.e., the ratio of annual tritium surface loading W (Bq. m -2 .s -1 ) and annual mean tritium concentration in air, c 0 (Bq.m -3 ) at three locations for the years 2011 is found to be 6.12E-04 to 2.89E-03. The average value for wet deposition velocity V w for NAPS site is estimated as 3.17E-03 m.s -1 . (author)

  2. ZEPHYR tritium system

    International Nuclear Information System (INIS)

    Swansiger, W.; Andelfinger, C.; Buchelt, E.; Fink, J.; Sandmann, W.; Stimmelmayr, A.; Wegmann, H.G.; Weichselgartner, H.

    1982-04-01

    The ignition experiment ZEPHYR will need tritium as an essential component of the fuel. The ZEPHYR Tritium Systems are designed as to recycle the fuel directly at the experiment. An amount of tritium, which is significantly below the total throughput, for example 10 5 Ci will be stored in uranium getters and introduced into the torus by a specially designed injection system. The torus vacuum system operates with tritium-tight turbomolecular pumps and multi-stage roots pumps in order to extract and store the spent fuel in intermediate storage tanks at atmospheric pressure. A second high vacuum system, similar in design, serves as to evacuate the huge containments of the neutral injection system. The spent fuel will be purified and subsequently processed by an isotope separation system in which the species D 2 , DT and T 2 will be recovered for further use. This isotope separation will be achieved by a preparative gaschromatographic process. All components of the tritium systems will be installed within gloveboxes which are located in a special tritium handling room. The atmospheres of the gloveboxes and of the tritium rooms are controlled by a tritium monitor system. In the case of a tritium release - during normal operation as well as during an accident - these atmospheres become processed by efficient tritium absorption systems. All ZEPHYR tritium handling systems are designed as to minimize the quantity of tritium released to the environment, so that the stringent German laws on radiological protection are satisfied. (orig.)

  3. Determination and maintenance of DE minimis risk for migration of residual tritium (3H) from the 1969 Project Rulison nuclear test to nearby hydraulically fractured natural gas wells.

    Science.gov (United States)

    Daniels, Jeffrey I; Chapman, Jenny B

    2013-05-01

    The Project Rulison underground nuclear test was a proof-of-concept experiment that was conducted under the Plowshare Program in 1969 in the Williams Fork Formation of the Piceance Basin in west-central Colorado. Today, commercial production of natural gas is possible from low permeability, natural gas bearing formations like that of the Williams Fork Formation using modern hydraulic fracturing techniques. With natural gas exploration and production active in the Project Rulison area, this human health risk assessment was performed in order to add a human health perspective for site stewardship. Tritium (H) is the radionuclide of concern with respect to potential induced migration from the test cavity leading to subsequent exposure during gas-flaring activities. This analysis assumes gas flaring would occur for up to 30 d and produce atmospheric H activity concentrations either as low as 2.2 × 10 Bq m (6 × 10 pCi m) from the minimum detectable activity concentration in produced water or as high as 20.7 Bq m (560 pCi m), which equals the highest atmospheric measurement reported during gas-flaring operations conducted at the time of Project Rulison. The lifetime morbidity (fatal and nonfatal) cancer risks calculated for adults (residents and workers) and children (residents) from inhalation and dermal exposures to such activity concentrations are all below 1 × 10 and considered de minimis. The implications for monitoring production water for conforming health-protective, risk-based action levels also are examined.

  4. Metabolism and dosimetry of tritium

    International Nuclear Information System (INIS)

    Hill, R.L.; Johnson, J.R.

    1993-01-01

    This document was prepared as a review of the current knowledge of tritium metabolism and dosimetry. The physical, chemical, and metabolic characteristics of various forms of tritium are presented as they pertain to performing dose assessments for occupational workers and for the general public. For occupational workers, the forms of tritium discussed include tritiated water, elemental tritium gas, skin absorption from elemental tritium gas-contaminated surfaces, organically bound tritium in pump oils, solvents and other organic compounds, metal tritides, and radioluminous paints. For the general public, age-dependent tritium metabolism is reviewed, as well as tritiated water, elemental tritium gas, organically bound tritium, organically bound tritium in food-stuffs, and tritiated methane. 106 refs

  5. Design of a tritium gas cell for beta-ray induced X-ray spectrometry using Monte Carlo simulation

    Energy Technology Data Exchange (ETDEWEB)

    Hara, Masanori, E-mail: masahara@ctg.u-toyama.ac.jp [Hydrogen Isotope Research Center, Organization for Promotion of Research, University of Toyama, 3190 Gofuku, Toyama City, Toyama 930-8555 (Japan); Abe, Shinsuke; Matsuyama, Masao [Hydrogen Isotope Research Center, Organization for Promotion of Research, University of Toyama, 3190 Gofuku, Toyama City, Toyama 930-8555 (Japan); Aso, Tsukasa [Electronics and Computer Engineering, National Institute of Technology, Toyama College, 1-2 Ebie-neriya, Imizu City, Toyama 933-0293 (Japan); Tatenuma, Katsuyoshi; Kawakami, Tomohiko; Ito, Takeshi [KAKEN Company Limited, 1044 Horimachi, Mito City, Ibaraki 310-0903 (Japan)

    2017-06-15

    Highlights: • Beta-ray induced X-ray spectrometry (BIXS) is a method for tritium gas analysis. • Gas cell for BIXS was designed by Monte Carlo simulations. • The optimum thickness of the gold layer on a beryllium window was around 150 nm. • This simulation model considered the self-absorption with increasing the cell length. - Abstract: One of the methods used for tritium gas analysis is beta-ray induced X-ray spectrometry (BIXS). Gas cell design is important in this method. The structure of the gas cell for BIXS was optimized by Monte Carlo simulation of beta-ray induced X-ray spectra in various window geometries using the Geant4 tool kit (version 10.01.p02). The simulated spectrum from tritium decay fitted the observed one, and the simulation model was used to obtain the cell parameters for BIXS. The optimum thickness of the gold layer on a beryllium window was around 150 nm. This simulation model also considered the relationship between self-absorption by hydrogen gas and the cell length. Self-absorption increased with increasing cell length and the relationship between the sample pressure and cell length was formulated.

  6. Tritium Systems Test Facility. Volume I

    International Nuclear Information System (INIS)

    Anderson, G.W.; Battleson, K.W.; Bauer, W.

    1976-10-01

    Sandia Laboratories proposes to build and operate a Tritium Systems Test Facility (TSTF) in its newly completed Tritium Research Laboratory at Livermore, California (see frontispiece). The facility will demonstrate at a scale factor of 1:200 the tritium fuel cycle systems for an Experimental Power Reactor (EPR). This scale for each of the TSTF subsystems--torus, pumping system, fuel purifier, isotope separator, and tritium store--will allow confident extrapolation to EPR dimensions. Coolant loop and reactor hall cleanup facilities are also reproduced, but to different scales. It is believed that all critical details of an EPR tritium system will be simulated correctly in the facility. Tritium systems necessary for interim devices such as the Ignition Test Reactor (ITR) or The Next Step (TNS) can also be simulated in TSTF at other scale values. The active tritium system will be completely enclosed in an inert atmosphere glove box which will be connected to the existing Gas Purification System (GPS) of the Tritium Research Laboratory. In effect, the GPS will become the scaled environmental control system which otherwise would have to be built especially for the TSTF

  7. TRIF - an intermediate approach to environmental tritium modelling

    International Nuclear Information System (INIS)

    Higgins, N.A.

    1997-01-01

    The movement of tritium through the environment, from an initial atmospheric release to selected end points in the food chain, involves a series of closely coupled and complex processes which are, consequently, difficult to model. TRIF (tritium transfer into food) provides a semi-empirical approach to this transport problem, which can be adjusted to bridge the gap between simple steady state approximations and a fully coupled model of tritium dispersion and migration (Higgins et al., 1996). TRIF provides a time-dependent description of the behaviour of tritium in the form of tritium gas (HT) and tritiated water (HTO) as it enters and moves through the food chain into pasture, crops and animals. This includes a representation of the production and movement of organically bound tritium (OBT). (Author)

  8. Oxidative Tritium Decontamination System

    International Nuclear Information System (INIS)

    Gentile, Charles A.; Parker, John J.; Guttadora, Gregory L.; Ciebiera, Lloyd P.

    2002-01-01

    The Princeton Plasma Physics Laboratory, Tritium Systems Group has developed and fabricated an Oxidative Tritium Decontamination System (OTDS), which is designed to reduce tritium surface contamination on various components and items. The system is configured to introduce gaseous ozone into a reaction chamber containing tritiated items that require a reduction in tritium surface contamination. Tritium surface contamination (on components and items in the reaction chamber) is removed by chemically reacting elemental tritium to tritium oxide via oxidation, while purging the reaction chamber effluent to a gas holding tank or negative pressure HVAC system. Implementing specific concentrations of ozone along with catalytic parameters, the system is able to significantly reduce surface tritium contamination on an assortment of expendable and non-expendable items. This paper will present the results of various experimentation involving employment of this system

  9. Tritium activities in Canada

    International Nuclear Information System (INIS)

    Gierszewski, P.

    1995-01-01

    Canadian tritium activites comprise three major interests: utilites, light manufacturers, and fusion. There are 21 operating CANDU reactors in Canada; 19 with Ontario Hydro and one each with Hydro Quebec and New Brunswick Power. There are two light manufacturers, two primary tritium research facilities (at AECL Chalk River and Ontario Hydro Technologies), and a number of industry and universities involved in design, construction, and general support of the other tritium activities. The largest tritum program is in support of the CANDU reactors, which generate tritium in the heavy water as a by-product of normal operation. Currently, there are about 12 kg of tritium locked up in the heavy water coolant and moderator of these reactors. The fusion work is complementary to the light manufacturing, and is concerned with tritium handling for the ITER program. This included design, development and application of technologies related to Isotope Separation, tritium handling, (tritiated) gas separation, tritium-materials interaction, and plasma fueling

  10. Molecular gas species in the lunar atmosphere

    International Nuclear Information System (INIS)

    Hoffman, J.H.; Hodges, R.R. Jr.

    1975-01-01

    There is good evidence for the existence of very small amounts of methane, ammonia and carbon dioxide in the very tenuous lunar atmosphere which consists primarily of the rare gases helium, neon and argon. All of these gases, except 40 Ar, originate from solar wind particles which impinge on the lunar surface and are imbedded in the surface material. Here they may form molecules before being released into the atmosphere, or may be released directly, as is the case for rare gases. Evidence for the existence of the molecular gas species is based on the pre-dawn enhancement of the mass peaks attributable to these compounds in the data from the Apollo 17 Lunar Mass Spectrometer. Methane is the most abundant molecular gas but its concentration is exceedingly low, 1 x 10 3 mol cm -3 , slightly less than 36 Ar, whereas the solar wind flux of carbon is approximately 2000 times that of 36 Ar. Several reasons are advanced for the very low concentration of methane in the lunar atmosphere

  11. Tritium immobilisation

    International Nuclear Information System (INIS)

    Bridger, N.J.

    1982-01-01

    Tritium is immobilised for long term storage by absorption in a hydridable/tritidable material, such as zirconium. A gas permeable container is packed with the material in the form of sponge fragments, rods or tubes, and a gaseous mixture of hydrogen and tritium introduced into the container whilst the container is at a temperature of about 600 deg C or above. Thermal expansion of the material during reaction with the gaseous mixture compacts the material into a coherent body in the container relatively free from finely divided hydride/ tritide material. (author)

  12. A method for assessing the annual dose to the most exposed individual from tritium and 14C reactor discharges to atmosphere

    International Nuclear Information System (INIS)

    Nair, S.

    1979-10-01

    A method is described for assessing the annual dose to the most exposed individual from routine releases of tritium and 14 C to the atmosphere during normal reactor operations. A detailed assessment has been made of the resulting equilibrium contamination levels in a range of foodstuffs typical of an average UK diet and of the annual doses resulting from a chronic intake of tritium and 14 C via inhalation, ingestion and, additionally, in the case of tritium, via skin absorption. Equilibrium annual doses from the global circulation of tritium and 14 C have also been calculated. Upper limits to the effective annual dose-equivalents to the most exposed individual were found to be 0.6 rem.yr -1 and 100 rem.yr -1 per Ci.yr -1 release of tritium and 14 C respectively, with the ingestion pathway contributing significantly to the overall exposure. The most exposed individual was found to be a Reference 10 year old child. The methods outlined for calculating the ingestion dose from tritium and 14 C releases hav been incorporated into the more generally applicable code FOODDOSE. The code may be used to make more realistic dose calculations to the individuals based on site-specific surveys of variables such as local meteorology, local diet and local land use for agriculture, which may lead to doses smaller than the upper limit values quoted by factors of 20 and 200 for tritium and 14 C respectively. (author)

  13. Tritium pellet injector results

    International Nuclear Information System (INIS)

    Fisher, P.W.; Bauer, M.L.; Baylor, L.R.; Deleanu, L.E.; Fehling, D.T.; Milora, S.L.; Whitson, J.C.

    1988-01-01

    Injection of solid tritium pellets is considered to be the most promising way of fueling fusion reactors. The Tritium Proof-of- Principle (TPOP) experiment has demonstrated the feasibility of forming and accelerating tritium pellets. This injector is based on the pneumatic pipe-gun concept, in which pellets are formed in situ in the barrel and accelerated with high-pressure gas. This injector is ideal for tritium service because there are no moving parts inside the gun and because no excess tritium is required in the pellet production process. Removal of 3 He from tritium to prevent blocking of the cryopumping action by the noncondensible gas has been demonstrated with a cryogenic separator. Pellet velocities of 1280 m/s have been achieved for 4-mm-diam by 4-mm-long cylindrical tritium pellets with hydrogen propellant at 6.96 MPa (1000 psi). 10 refs., 10 figs

  14. Development of dose assessment code for release of tritium during normal operation of nuclear power plants

    International Nuclear Information System (INIS)

    Duran, J.; Malatova, I.

    2009-01-01

    A computer code PTM H TO has been developed to assess tritium doses to the general public. The code enables to simulate the behavior of tritium in the environment released into the atmosphere under normal operation of nuclear power plants. Code can calculate the doses for the three chemical and physical forms: tritium gas (HT), tritiated water vapor and water drops (HTO). The models in this code consist of the tritium transfer model including oxidation of HT to HTO and reemission of HTO from soil to the atmosphere, and the dose calculation model

  15. Sources of tritium

    International Nuclear Information System (INIS)

    Phillips, J.E.; Easterly, C.E.

    1980-12-01

    A review of tritium sources is presented. The tritium production and release rates are discussed for light water reactors (LWRs), heavy water reactors (HWRs), high temperature gas cooled reactors (HTGRs), liquid metal fast breeder reactors (LMFBRs), and molten salt breeder reactors (MSBRs). In addition, release rates are discussed for tritium production facilities, fuel reprocessing plants, weapons detonations, and fusion reactors. A discussion of the chemical form of the release is included. The energy producing facilities are ranked in order of increasing tritium production and release. The ranking is: HTGRs, LWRs, LMFBRs, MSBRs, and HWRs. The majority of tritium has been released in the form of tritiated water

  16. Hazardous gas treatment by atmospheric discharges

    International Nuclear Information System (INIS)

    Mizeraczyk, J.

    2005-01-01

    The emissions of NO x ; SO x , CO 2 and volatile organic compounds (VOCs) including fluorocarbons to the atmosphere influence heavily our environment, NO x and SO x emitted to the atmosphere are the major cause of acid rains, while CO 2 and VOCs emissions cause the greenhouse effect which leads to abnormal global heating of the atmosphere and creating in a temperature inversion layer that traps gaseous pollutants. Therefore, there is an increasing interest in controlling these emissions. A new technique, which uses the plasma processes induced by energetic electrons, emerges as one of the most effective methods of reducing concentrations of the emitted gaseous pollutants. Various plasma techniques have been tested for gaseous pollution control. The electron bean irradiation was found to be physically and economically efficient for NO x and SO x reduction in the exhaust gases from electrical and heat power plants. The capability of the non-thermal plasmas, produced in atmospheric pressure electrical discharges, for decomposition of the gaseous pollutants has been widely tested. These atmospheric pressure electrical discharges are dielectric barrier discharges, pulsed and de corona discharges (in the reactors with the point-to-plate, wire-cylinder and wire-plate geometries, in the reactors with flow stabilized corona torch and corona radical shower), gliding discharges, inductively coupled high-frequency discharges, ac surface discharges, ac discharges in the packed bed reactors, and microwave torch discharges. In this paper, after reviewing the methods and devices used for producing the non-thermal plasmas for gaseous pollutant control, some results of the laboratory experiments on the plasmas abatement of NO x ; SO x and various VOCs will be presented, followed by a discussion on the energy efficiency and by-products. Also some results obtained in the pilot-plants will be given. finally other possible applications of the presented plasma devices for controlling

  17. The hazard to man of accidental releases of tritium

    International Nuclear Information System (INIS)

    Brearley, I.R.

    1985-03-01

    Some aspects of the atmospheric dispersion of tritium are discussed, followed by consideration of the dosimetric pathways. In order to assess the significance of a tritium release the doses from various pathways are estimated and compared with the doses estimated from a similar release of iodine-131. The major hazard from tritium is the ingestion of contaminated food products. For similar releases of tritium and I 131 the ingestion hazard can be comparable if the release occurs near and before the end of the harvest season. However, in the tritium release case the agricultural season influences the consequences markedly and, at other times during the year, the ingestion hazard from tritium may be approximately 20 times less. The dose from inhalation of tritium is sensitive to its chemical form and for similar releases of tritiated water and tritium gas then the dose from tritiated water is approximately 10 4 greater than the dose from tritium gas. For similar releases of tritiated water and iodine-131 then a comparison of the inhalation shows that the dose from the iodine is approximately 300 times greater. (author)

  18. Geostatistical analysis of tritium, groundwater age and other noble gas derived parameters in California.

    Science.gov (United States)

    Visser, A; Moran, J E; Hillegonds, Darren; Singleton, M J; Kulongoski, Justin T; Belitz, Kenneth; Esser, B K

    2016-03-15

    Key characteristics of California groundwater systems related to aquifer vulnerability, sustainability, recharge locations and mechanisms, and anthropogenic impact on recharge are revealed in a spatial geostatistical analysis of a unique data set of tritium, noble gases and other isotopic analyses unprecedented in size at nearly 4000 samples. The correlation length of key groundwater residence time parameters varies between tens of kilometers ((3)H; age) to the order of a hundred kilometers ((4)Heter; (14)C; (3)Hetrit). The correlation length of parameters related to climate, topography and atmospheric processes is on the order of several hundred kilometers (recharge temperature; δ(18)O). Young groundwater ages that highlight regional recharge areas are located in the eastern San Joaquin Valley, in the southern Santa Clara Valley Basin, in the upper LA basin and along unlined canals carrying Colorado River water, showing that much of the recent recharge in central and southern California is dominated by river recharge and managed aquifer recharge. Modern groundwater is found in wells with the top open intervals below 60 m depth in the southeastern San Joaquin Valley, Santa Clara Valley and Los Angeles basin, as the result of intensive pumping and/or managed aquifer recharge operations. Copyright © 2016 Elsevier Ltd. All rights reserved.

  19. Atmospheric tritium concentrations under influence of AREVA NC La Hague reprocessing plant (France) and background levels.

    Science.gov (United States)

    Connan, O; Hébert, D; Solier, L; Maro, D; Pellerin, G; Voiseux, C; Lamotte, M; Laguionie, P

    2017-10-01

    In-air tritium measurements were conducted around the AREVA NC La Hague reprocessing plant, as well as on other sites that are not impacted by the nuclear industry in northwest of France. The results indicate that the dominant tritium form around the AREVA site is HT (86%). HT and HTO levels are lower than 5 and 1 Bq. m -3 for hourly samples taken in the plume. No tritiated organic molecules (TOM) were detected. 26 measurement campaigns were performed and links were established between near-field 85 Kr, HT and HTO activities. Environmental measurements are in line with those taken at the discharge stack, and tend to demonstrate that there are no rapid changes in the tritium forms released. Out of the influence of any nuclear activities, the levels measured were below 13 mBq.m -3 for HT and 5 mBq.m -3 for HTO (<0.5 Bq. L -1 ). HTO level in air seems to be influenced by HTO activities in surrounding seawater. Copyright © 2017 Elsevier Ltd. All rights reserved.

  20. TFTR tritium handling concepts

    International Nuclear Information System (INIS)

    Garber, H.J.

    1976-01-01

    The Tokamak Fusion Test Reactor, to be located on the Princeton Forrestal Campus, is expected to operate with 1 to 2.5 MA tritium--deuterium plasmas, with the pulses involving injection of 50 to 150 Ci (5 to 16 mg) of tritium. Attainment of fusion conditions is based on generation of an approximately 1 keV tritium plasma by ohmic heating and conversion to a moderately hot tritium--deuterium ion plasma by injection of a ''preheating'' deuterium neutral beam (40 to 80 keV), followed by injection of a ''reacting'' beam of high energy neutral deuterium (120 to 150 keV). Additionally, compressions accompany the beam injections. Environmental, safety and cost considerations led to the decision to limit the amount of tritium gas on-site to that required for an experiment, maintaining all other tritium in ''solidified'' form. The form of the tritium supply is as uranium tritide, while the spent tritium and other hydrogen isotopes are getter-trapped by zirconium--aluminum alloy. The issues treated include: (1) design concepts for the tritium generator and its purification, dispensing, replenishment, containment, and containment--cleanup systems; (2) features of the spent plasma trapping system, particularly the regenerable absorption cartridges, their integration into the vacuum system, and the handling of non-getterables; (3) tritium permeation through the equipment and the anticipated releases to the environment; (4) overview of the tritium related ventilation systems; and (5) design bases for the facility's tritium clean-up systems

  1. The tritium operations experience on TFTR

    International Nuclear Information System (INIS)

    Halle, A. von; Anderson, J.L.; Gentile, C.; Grisham, L.; Hosea, J.; Kamperschroer, J.; LaMarche, P.; Oldaker, M.; Nagy, A.; Raftopoulos, S.; Stevenson, T.

    1995-01-01

    The Tokamak Fusion Test Reactor (TFTR) tritium gas system is administratively limited to 5 grams of tritium and provides the feedstock gas for the neutral beam and torus injection systems. Tritium operations on TFTR began with leak checking of gas handling systems, qualification of the gas injection systems, and high power plasma operations using trace amounts of tritium in deuterium feedstock gas. Full tritium operation commenced with four highly diagnosed neutral beam pulses into a beamline calorimeter to verify planned tritium beam operating routines and to demonstrate the deuterium to tritium beam isotope exchange. Since that time, TFTR has successfully operated each of the twelve neutral beam ion sources in tritium during hundreds of tritium beam pulses and torus gas injections. This paper describes the TFTR tritium gas handling systems and TFTR tritium operations of the gas injection systems and the neutral beam ion sources. Tritium accounting and accountability is discussed, including tritium retention issues of the torus limiters and beam impinged surfaces of the beamline components. Also included is tritium beam velocity analysis that compares the neutral beam extracted ion species composition for deuterium and tritium and that determines the extent of beam isotope exchange on subsequent deuterium and tritium beam pulses. The required modifications to TFTR operating routines to meet the U.S. Department of Energy regulations for a low hazard nuclear facility and the problems encountered during initial tritium operations are described. (orig.)

  2. The tritium operations experience on TFTR

    International Nuclear Information System (INIS)

    von Halle, A.; Gentile, C.

    1994-01-01

    The Tokamak Fusion Test Reactor (TFTR) tritium gas system is administratively limited to 5 grains of tritium and provides the feedstock gas for the neutral beam and torus injection systems. Tritium operations on TFTR began with leak checking of gas handling systems, qualification of the gas injection systems, and high power plasma operations using using trace amounts of tritium in deuterium feedstock gas. Full tritium operation commenced with four highly diagnosed neutral beam pulses into a beamline calorimeter to verify planned tritium beam operating routines and to demonstrate the deuterium to tritium beam isotope exchange. Since that time, TFTR has successfully operated each of the twelve neutral beam ion sources in tritium during hundreds of tritium beam pulses and torus gas injections. This paper describes- the TFTR tritium gas handling systems and TFTR tritium operations of the gas injection systems and the neutral beam ion sources. Tritium accounting and accountability is discussed, including tritium retention issues of the torus limiters and beam impinged surfaces of the beamline components. Also included is tritium beam velocity analysis that compares the neutral beam extracted ion species composition for deuterium and tritium and that determines the extent of beam isotope exchange on subsequent deuterium and tritium beam pulses. The required modifications to TFTR operating routines to meet the US Department of Energy regulations for a low hazard nuclear facility and the problems encountered during initial tritium operations are described

  3. Tritium conference days

    International Nuclear Information System (INIS)

    Garnier-Laplace, J.; Lebaron-Jacobs, L.; Sene, M.; Devin, P.; Chretien, V.; Le Guen, B.; Guetat, Ph.; Baglan, N.; Ansoborlo, E.; Boyer, C.; Masson, M.; Bailly-Du-Bois, P.; Jenkinson, St.; Wakeford, R.; Saintigny, Y.; Romeo, P.H.; Thompson, P.; Leterq, D.; Chastagner, F.; Cortes, P.; Philippe, M.; Paquet, F.; Fournier, M.

    2009-01-01

    This document gathers the slides of the available presentations given during this conference day. Twenty presentations out of 21 are assembled in the document and deal with: 1 - tritium in the environment (J. Garnier-Laplace); 2 - status of knowledge about tritium impact on health (L. Lebaron-Jacobs); 3 - tritium, discrete but present everywhere (M. Sene); 4 - management of tritium effluents from Areva NC La Hague site - related impact and monitoring (P. Devin); 5 - tritium effluents and impact in the vicinity of EDF's power plants (V. Chretien and B. Le Guen); 6 - contribution of CEA-Valduc centre monitoring to the knowledge of atmospheric tritiated water transfers to the different compartments of the environment (P. Guetat); 7 - tritium analysis in environment samples: constraints and means (N. Baglan); 8 - organically-linked tritium: the analyst view (E. Ansoborlo); 9 - study of tritium transfers to plants via OBT/HTO air and OBT/HTO free (C. Boyer); 10 - tritium in the British Channel (M. Masson and P. Bailly-Du-Bois); 11 - tritium in British coastal waters (S. Jenkinson); 12 - recent results from epidemiology (R. Wakeford); 13 - effects of tritiated thymidine on hematopoietic stem cells (P.H. Romeo); 14 - tritium management issue in Canada: the point of view from authorities (P. Thompson); 15 - experience feedback of the detritiation process of Valduc centre (D. Leterq); 16 - difficulties linked with tritiated wastes confinement (F. Chastagner); 17 - optimisation of tritium management in the ITER project (P. Cortes); 18 - elements of thought about the management of tritium generated by nuclear facilities (M. Philippe); 19 - CIPR's position about the calculation of doses and risks linked with tritium exposure (F. Paquet); 20 - tritium think tanks (M. Fournier). (J.S.)

  4. The Separation of Hydrogen Tritium and Tritium Hydride by Gas Chromatography; Separation de l'hydrogene, du tritium et de l'hydrure de tritium par chromatographic en phase gazeuse; Razdelenie vodoroda, tritiya i gidrida tritiya posredstvom gazovoj khromatografii; Separacion del hidrogeno, tritio e hidruro de tritio por cromatografia de gases

    Energy Technology Data Exchange (ETDEWEB)

    Smith, H A; Carter, Jr, E H [University of Tennessee, Knoxville, TN (United States)

    1962-01-15

    Now that successful separation of hydrogen, deuterium and hydrogen deuteride has been achieved by gas chromatography, similar studies are being made dealing with mixtures of hydrogen, tritium and tritium hydride. Since tritium is used in tracer quantities the usual katharometer cannot be employed for its detection. This difficulty has been overcome by providing immediately following the katharometer a vibrating reed electrometer equipped with a high resistance leak which allows continuous monitoring of the activity of any tritium or tritium hydride emerging from the column by means of synchronized recorders. Separation of such mixtures has been tested with columns packed with palladium on silica, silica, alumina, and alumina coated with chromium oxide or ferric oxide. No effective separation was obtained with the palladium on silica column. Good separation was achieved with the plain silica column where hydrogen was employed as the carrier gas, but helium failed to elute the isotopes. Satisfactory results were obtained with the coated, partially deactivated alumina packing when helium or neon was the carrier gas, but the best separation was found with a column packing of uncoated activated alumina. Calibration with helium-tritium mixtures of known activity plus equilibrated hydrogen-tritium mixtures also of known activity allows quantitative estimation of tritium and tritium hydride. (author) [French] La separation de l'hydrogene, du deuterium et du deuterure d'hydrogene par chromatographic en phase gazeuse ayant ete realisee, on procede maintenant a des etudes semblables sur des melanges d'hydrogene de tritium et d'hydrure de tritium. Comme le tritium n'est present qu'en quantites infimes, on ne peut utiliser le catharometre ordinaire pour le detecter. On a surmonte cette difficulte en faisant suivre le catharometre d'un electrometre a lame vibrante, muni d'une fuite haute resistance, qui permet de mesurer, a l'aide d'enregistreurs synchronises, l'activite de

  5. Tritium control: October 1982-March 1983

    International Nuclear Information System (INIS)

    Lamberger, P.H.; Rogers, M.L.

    1983-01-01

    Surveys in gloveboxes indicated surface activity on stainless steel and its apparent dependence on time and atmospheric tritium levels. Surveys in fumehoods were completed to investigate the extent of surface contamination on surfaces of various materials. Gas generation rates caused by radiolysis of tritiated waste materials were determined for polymer and nonpolymer-impregnated tritiated concrete and fixated and nonfixated tritiated waste vacuum pump oil. In addition, the pressure change of hydrogen cover gas over tritiated water on cement-plaster was determined. The test program to measure and compare the release of tritium from tritiated concrete with and without styrene impregnation continued. Tritium permeation data from small test blocks are given. The drum study monitoring the release of tritium from actual burial packages continued. The maximum fractional release rate for the three types of high activity, tritiated liquid waste generated is 5.1 x 10 -5 , and the maximum total permeation is 179 mCi after 8.5 yr. These two values represent a 13% increase for the past 6 months. Tritium release from the polymer-impregnated, tritiated concrete (PITC) and from the control (non-PITC) remains very low. The Emergency Containment System (ECS), an automatically actuated system developed at Mound to remove tritium from room air, has been modified and upgraded to support new applications. The leakage rate in the ECS area has been lowered, a fast-start system installed for greater conversion efficiency at startup, and the alumina beds regenerated

  6. Assessment of a chemical getter for scavenging tritium from an inert gas

    International Nuclear Information System (INIS)

    Maienschein, J.L.

    1976-01-01

    Results are presented of a study aimed at determining the feasibility of using chemical getter beds to scavenge tritium from inert gases. Two types of getter bed, fixed and fluidized, were considered, using cerium as the getter material. Mathematical-modeling results and capital-cost estimates indicate that not only is the gettering approach technically feasible, it could lead to considerable cost savings over catalytic oxidation, the tritium-removal method traditionally used

  7. Torrefaction of empty fruit bunches under biomass combustion gas atmosphere.

    Science.gov (United States)

    Uemura, Yoshimitsu; Sellappah, Varsheta; Trinh, Thanh Hoai; Hassan, Suhaimi; Tanoue, Ken-Ichiro

    2017-11-01

    Torrefaction of oil palm empty fruit bunches (EFB) under combustion gas atmosphere was conducted in a batch reactor at 473, 523 and 573K in order to investigate the effect of real combustion gas on torrefaction behavior. The solid mass yield of torrefaction in combustion gas was smaller than that of torrefaction in nitrogen. This may be attributed to the decomposition enhancement effect by oxygen and carbon dioxide in combustion gas. Under combustion gas atmosphere, the solid yield for torrefaction of EFB became smaller as the temperature increased. The representative products of combustion gas torrefaction were carbon dioxide and carbon monoxide (gas phase) and water, phenol and acetic acid (liquid phase). By comparing torrefaction in combustion gas with torrefaction in nitrogen gas, it was found that combustion gas can be utilized as torrefaction gas to save energy and inert gas. Copyright © 2017 Elsevier Ltd. All rights reserved.

  8. Tritium sampling and measurement

    International Nuclear Information System (INIS)

    Wood, M.J.; McElroy, R.G.; Surette, R.A.; Brown, R.M.

    1993-01-01

    Current methods for sampling and measuring tritium are described. Although the basic techniques have not changed significantly over the last 10 y, there have been several notable improvements in tritium measurement instrumentation. The design and quality of commercial ion-chamber-based and gas-flow-proportional-counter-based tritium monitors for tritium-in-air have improved, an indirect result of fusion-related research in the 1980s. For tritium-in-water analysis, commercial low-level liquid scintillation spectrometers capable of detecting tritium-in-water concentrations as low as 0.65 Bq L-1 for counting times of 500 min are available. The most sensitive method for tritium-in-water analysis is still 3He mass spectrometry. Concentrations as low as 0.35 mBq L-1 can be detected with current equipment. Passive tritium-oxide-in-air samplers are now being used for workplace monitoring and even in some environmental sampling applications. The reliability, convenience, and low cost of passive tritium-oxide-in-air samplers make them attractive options for many monitoring applications. Airflow proportional counters currently under development look promising for measuring tritium-in-air in the presence of high gamma and/or noble gas backgrounds. However, these detectors are currently limited by their poor performance in humidities over 30%. 133 refs

  9. High-pressure tritium

    International Nuclear Information System (INIS)

    Coffin, D.O.

    1976-01-01

    Some solutions to problems of compressing and containing tritium gas to 200 MPa at 700 0 K are discussed. The principal emphasis is on commercial compressors and high-pressure equipment that can be easily modified by the researcher for safe use with tritium. Experience with metal bellows and diaphragm compressors has been favorable. Selection of materials, fittings, and gauges for high-pressure tritium work is also reviewed briefly

  10. Radionuclide Basics: Tritium

    Science.gov (United States)

    Tritium is a hydrogen atom that has two neutrons in the nucleus and one proton. It is radioactive and behaves like other forms of hydrogen in the environment. Tritium is produced naturally in the upper atmosphere and as a byproduct of nuclear fission.

  11. Design and test about de tritium system to filling tritium glove box

    International Nuclear Information System (INIS)

    Lei, Jiarong; Du, Yang; Yang, Yong

    2008-01-01

    In order to deal tritium permeated from inflating tritium system at the scene of inflating tritium, dealing waste tritium gas system was designed according to demand and action of dealing waste tritium gas from inflating tritium, and the data of character and volume about appliance of catalyst reaction and drying agent was calculated. Through the test at the scene of inflating tritium, it is result that dealing waste tritium gas system's efficiency reaches above 85% average in circulatory system, so that it can be used in practice extensively. (author)

  12. Treatment of tritiated exhaust gases at the Tritium Laboratory Karlsruhe

    Energy Technology Data Exchange (ETDEWEB)

    Hutter, E.; Besserer, U. [Kernforschungszentrum Karlsruhe GmbH (Germany); Jacqmin, G. [NUKEM GmbH, Industreistr, Alzenau (Germany)

    1995-02-01

    The Tritium Laboratory Karlsruhe (TLK) accomplished commissioning; tritium involving activities will start this year. The laboratory is destined mainly to investigating processing of fusion reactor fuel and to developing analytic devices for determination of tritium and tritiated species in view of control and accountancy requirements. The area for experimental work in the laboratory is about 800 m{sup 2}. The tritium infrastructure including systems for tritium storage, transfer within the laboratory and processing by cleanup and isotope separation methods has been installed on an additional 400 m{sup 2} area. All tritium processing systems (=primary systems), either of the tritium infrastructure or of the experiments, are enclosed in secondary containments which consist of gloveboxes, each of them connected to the central depressurization system, a part integrated in the central detritiation system. The atmosphere of each glovebox is cleaned in a closed cycle by local detritiation units controlled by two tritium monitors. Additionally, the TLK is equipped with a central detritiation system in which all gases discharged from the primary systems and the secondary systems are processed. All detritiation units consist of a catalyst for oxidizing gaseous tritium or tritiated hydrocarbons to water, a heat exchanger for cooling the catalyst reactor exhaust gas to room temperature, and a molecular sieve bed for adsorbing the water. Experiments with tracer amounts of tritium have shown that decontamination factors >3000 can be achieved with the TLK detritiation units. The central detritiation system was carefully tested and adjusted under normal and abnormal operation conditions. Test results and the behavior of the tritium barrier preventing tritiated exhaust gases from escaping into the atmosphere will be reported.

  13. Environmental tritium in trees

    International Nuclear Information System (INIS)

    Brown, R.M.

    1979-01-01

    The distribution of environmental tritium in the free water and organically bound hydrogen of trees growing in the vicinity of the Chalk River Nuclear Laboratories (CRNL) has been studied. The regional dispersal of HTO in the atmosphere has been observed by surveying the tritium content of leaf moisture. Measurement of the distribution of organically bound tritium in the wood of tree ring sequences has given information on past concentrations of HTO taken up by trees growing in the CRNL Liquid Waste Disposal Area. For samples at background environmental levels, cellulose separation and analysis was done. The pattern of bomb tritium in precipitation of 1955-68 was observed to be preserved in the organically bound tritium of a tree ring sequence. Reactor tritium was discernible in a tree growing at a distance of 10 km from CRNL. These techniques provide convenient means of monitoring dispersal of HTO from nuclear facilities. (author)

  14. Tritium in nuclear power plants

    International Nuclear Information System (INIS)

    Badyaev, V.V.; Egorov, Yu.A.; Sklyarov, V.P.; Stegachev, G.V.

    1981-01-01

    The problem of tritium formation during NPP operation is considered on the basis of available published data. Tritium characteristics are given, sources of the origin of natural and artificial tritium are described. NPP contribution to the total tritium amount in the environment is determined, as well as contribution of each process in the reactor to the quantity of tritium, produced at the NPP. Thermal- and fast-neutron reactions with tritium production are shown, their contribution to the total amount of tritium in a coolant is estimated, taking into account the type of reactor. Data on tritium content in NPP wastes and in the air of working premises are presented. Methods for sampling and sample preparation to measurements as well as the appropriate equipment are considered. Design of the gas-discharge counter of internal filling, used for measuring tritium activity in samples is described [ru

  15. Influence of hydrogen addition to a sweep gas on tritium behavior in a blanket module containing Li{sub 2}TiO{sub 3} pebbles

    Energy Technology Data Exchange (ETDEWEB)

    Katayama, K., E-mail: kadzu@nucl.kyushu-u.ac.jp [Department of Advanced Energy Engineering Science, Kyushu University 6-1, Kasugakoen, Kasuga-shi, Fukuoka 816-8580 (Japan); Someya, Y.; Tobita, K. [National Institutes for Quantum and radiological Science and Technology, 2-166 Omotedate, Obuchi, Rokkasho-mura, Kamikita-gun, Aomori 039-3212 (Japan); Fukada, S. [Department of Advanced Energy Engineering Science, Kyushu University 6-1, Kasugakoen, Kasuga-shi, Fukuoka 816-8580 (Japan); Hatano, Y. [Hydrogen Isotope Research Center, University of Toyama, Gofuku 3190, Toyama 930-8555 (Japan); Chikada, T. [Department of Chemistry, Graduate school of Science, Shizuoka University, 836 Ohya, Suruga-ku, Shizuoka, 422-8529 (Japan)

    2016-12-15

    Highlights: • Mass balance equations of H{sub 2}, H{sub 2}O, T{sub 2} and T{sub 2}O in a Li{sub 2}TiO{sub 3} pebble bed were numerically calculated. • In the temperature rising process, the pebbles were exposed to water vapor of relatively high concentration. • Tritium permeation rate to cooling water reduced with increasing hydrogen concentration in the sweep gas. • Tritium inventory in the grain bulk and the grain surface occupied 99.6% of total inventory. - Abstract: Hydrogen addition to a sweep gas of a solid breeder blanket module has been proposed to enhance tritium recovery from the surface of the breeders. However, the influence of hydrogen addition on the bred tritium behavior is not understood completely. Tritium behavior in the simplified blanket module of Li{sub 2}TiO{sub 3} pebbles was numerically calculated considering diffusion in the grain bulk, surface reactions on the grain surface and permeation through the cooling pipe. Although a partial pressure of T{sub 2} increases with increasing a partial pressure of H{sub 2} in the sweep gas, it was estimated that tritium permeation rate to the cooling water decreases. Additionally, the release duration of water vapor generated by the reaction of the pebbles and hydrogen is shortened with increasing a partial pressure of H{sub 2}. Tritium inventory in the grain bulk and the grain surface occupies 99.6 % of total tritium inventory in the blanket module.

  16. Tritium production distribution in the accelerator production of tritium device

    International Nuclear Information System (INIS)

    Kidman, R.B.

    1997-11-01

    Helium-3 ( 3 He) gas is circulated throughout the accelerator production of tritium target/blanket (T/B) assembly to capture neutrons and convert 3 He to tritium. Because 3 He is very expensive, it is important to know the tritium producing effectiveness of 3 He at all points throughout the T/B. The purpose of this paper is to present estimates of the spatial distributions of tritium production, 3 He inventory, and the 3 He FOM

  17. Contribution to the tritium continental effect

    International Nuclear Information System (INIS)

    Lewis, R.R.; Froehlich, K.; Hebert, D.

    1987-01-01

    The results of tritium measurements of atmospheric water vapour and precipitation samples for 1982 and 1983 are presented. The data were used to establish a simple model describing the tritium continental effect taking into account re-evaporation of tritium from the continental land surfaces and man-made tritium. (author)

  18. Contribution to the tritium continental effect

    International Nuclear Information System (INIS)

    Lewis, R.R.; Froehlich, K.; Hebert, D.

    1987-01-01

    The results of tritium measurements of atmospheric water vapour and precipitation samples for 1982 and 1983 are presented. The data were used to establish a simple model describing the tritium continental effect taking into account re-evaporation of tritium from the continental land surfaces. Some comments on man made tritium are given. (author)

  19. Observed and Modeled Tritium Concentrations in the Terrestrial Food Chain near a Continuous Atmospheric Source

    International Nuclear Information System (INIS)

    Davis, P.A.; Kim, S.B.; Chouhan, S.L.; Workman, W.J.G.

    2005-01-01

    Tritium concentrations were measured in a large number of environmental and biological samples collected during 2002 at two dairy farms and a hobby farm near Pickering Nuclear Generating Station in Ontario, Canada. The data cover most compartments of the terrestrial food chain in an agricultural setting and include detailed information on the diets of the local farm animals. Ratios of plant OBT concentration to air moisture HTO varied between 0.12 and 0.56, and were generally higher for the forage crops collected at the dairy farms than for the garden vegetables sampled at the hobby farm. Animal OBT to air HTO ratios were more uniform, ranging from 0.18 to 0.45, and were generally higher for the milk and beef samples from the dairy farms than for the chicken products from the hobby farm. The observed OBT concentrations in plants and animals were compared with predictions of IMPACT, the model used by the Canadian nuclear industry to calculate annual average doses due to routine releases. The model performed well on average for the animal endpoints but overestimated concentrations in plants by a factor of 2

  20. Experimental and modelling studies on the exposure of wall surfaces to tritium gas in ambient room conditions

    International Nuclear Information System (INIS)

    Housiadas, C.; Douglas, K.

    1995-01-01

    An experimental set-up is used to carry out static exposure tests to study the uptake and oxidation of tritium released in ambient room air, routinely or accidentally, in the presence of selected surface materials. Tritium, in its elemental form at concentrations of the order of approx.0.4 GBq/m 3 (10 -2 Ci/m 3 ), is injected into the glass exposure chamber containing the selected surface material and air at atmospheric pressure. Periodically, samples of the chamber atmosphere are analysed, using liquid scintillation counting, to obtain the concentrations of HTO and T 2 . The exposures have been performed using aluminium, 316L stainless steel and painted stainless steel plates, as the selected surface materials. Results are compared with predictions using the ITER approved TMAP4 code. The results indicate practically the same conversion rate, of about 0.02% per day, for both the aluminium and stainless steel samples and give reasonable agreement with modelling predictions. Strong absorption of both T 2 and HTO by the painted surface is observed, suggesting the use of high values for the solubility constant to correctly predict this behaviour. 19 refs., 5 figs., 1 tab

  1. Concentrations of tritium in atmospheric moisture and precipitation of Mt. Hakkoda

    International Nuclear Information System (INIS)

    Kimura, Hideki; Kon, Takezumi; Sasaki, Mamoru

    2000-01-01

    A large-scale spent nuclear fuel reprocessing plant in Japan is now under construction in Rokkasho Village, Aomori Prefecture. The 3 H will be one of the major radionuclides released from the plant. To grasp the behavior of 3 H in the environment in Aomori Prefecture, we surveyed 3 H concentrations in the atmospheric moisture and the precipitation samples at Mt. Hakkoda. Additional atmospheric moisture samples were collected at Rokkasho Village and Aomori City. The relatively high 3 H concentration in the atmospheric moisture and the precipitation samples at Mt. Hakkoda were observed from spring to summer. The 3 H concentrations in the precipitation were similar to those in the atmospheric moisture. The temporal variation patterns of 3 H concentrations in the atmospheric moisture were similar in relatively wide region that covers from Mt. Hakkoda to Aomori City and Rokkasho Village. The 3 H concentration in atmospheric moisture at the top of Mt. Hakkoda positively correlated with the ozone concentration. It suggested that 3 H originated from the stratosphere, and showed that ozone might be used as an indictor of background 3 H. (author)

  2. Metabolism of tritium uptake due to handling of metal surfaces exposed to tritiated hydrogen gas

    International Nuclear Information System (INIS)

    Johnson, J.R.; Peterman, B.F.

    1987-08-01

    Hairless rats were exposed to tritium by rubbing HT contaminated stainless steel planchets on them. The pattern of tritium excretion in the urine (n=4), shows the OBT (organically bound tritium) retention curve to be approximated by the sum of 2 exponential curves, one with a half-life of 0.4 days and another with a half-life of 1.4 days. The retention of HTO fit a single exponential curve with a half-life of 3.1 days. Exposed skin, unexposed skin, liver, muscle and blood (n=6) were assayed for HBO, and free HTO. Highest activity was found in the exposed skin, other organs with high activity are the unexposed skin and liver. Examination of the exposed skin showed HTO to be concentrated in the uppermost layers. The distribution of OBT was similar but was incorporated at a faster rate. The basal layer is exposed to a tritium concentration between 70-90% of that of the surface. The two macromolecule fractions with the highest amount of radioactivity were lipid and insoluble protein (mainly collagen)

  3. Study of atmospheric tritium transfers in lettuce: kinetic study, equilibrium and organic incorporation during a continuous atmospheric exposure; Etude des transferts du tritium atmospherique chez la laitue: Etude cinetique, etat d'equilibre et integration du tritum sous forme organique lors d'une exposition atmospherique continue

    Energy Technology Data Exchange (ETDEWEB)

    Boyer, C.

    2009-11-30

    This thesis has explored the mechanisms of tritium 'absorption and incorporation in a human-consumed plant, lettuce (Lactuca sativa L.), due to atmospheric exposure. Foliar uptake appears to play a key role in absorption of tritium as tissue free water tritium. Whatever the development stage and the light conditions, the specific activity in tissue free water reaches that of water vapour in air in several hours. The specific activity ratio is then about 0, 4. The time to reach equilibrium in soil is over 24 hours in most cases: the specific activity ratio ranges then 0, 01 to 0, 26. Incorporation rate of tissue free water tritium as organically-bound tritium has been estimated to 0, 13 to 0, 16 % h-l in average over the growing period of the plant, but marked variations are observed during growth. In particular, a significant increase appeared at the exponential growth stage. Deposition and diffusion of tritium in soil lead to significant OBT activities in soil. Results globally indicate equilibrium between the different environmental compartments (air, soil, plant). However, some experiments have revealed high OBT concentrations regarding atmospheric level exposure and ask for a possible phenomenon of local tritium accumulation in OBT for particular conditions of exposure. (author) [French] Ce travail de these a concerne l'etude des phenomenes d'absorption et d'incorporation sous forme organique du tritium dans un vegetal de consommation courante, la laitue (Lactuca sativa L.), en reponse a une exposition atmospherique. Il apparait que la voie foliaire joue un role primordial dans l'absorption du tritium au sein de l'eau tissulaire des plants. Quels que soient le stade de developpement des plants et les conditions d'eclairement, le temps necessaire pour atteindre l'equilibre des concentrations dans l'eau libre et dans la vapeur d'eau de l'air est de plusieurs heures; le rapport des concentrations est alors de

  4. Japanese university program on tritium radiobiology and environmental tritium

    International Nuclear Information System (INIS)

    Okada, Shigefumi

    1989-01-01

    The university program of the tritium study in the Special Research Project of Nuclear Fusion (1980-1989) is now on its 9th year. The study's aim is to assess tritium risk on man and environment for development of Japanese Nuclear Fusion Program. The tritium study begun by establishing various tritium safe-handling devices and methods to protect scientists from tritium contamination. Then, the tritium studies were initiated in three areas: The first was the studies on biological effects of tritiated water, where their RBE values, their modifying factors and mechanisms were investigated. Also, several human monitoring systems for detection of tritium-induced damage were developed. The second was the metabolic studies of tritium, including a daily tritium monitoring system, methods to enhance excretion of tritiated water from body and means to prevent oxidation of tritium gas in the body. The third was the study of environmental tritium. Tritium levels in environmental waters of various types were estimated all-over in Japan and their seasonal or regional variation were analyzed. Last two years, the studies were extended to estimate tritium activities of plants, foods and man in Japan. (author)

  5. Tritium storage

    International Nuclear Information System (INIS)

    Hircq, B.

    1990-01-01

    This document represents a synthesis relative to tritium storage. After indicating the main storage particularities as regards tritium, storages under gaseous and solid form are after examined before establishing choices as a function of the main criteria. Finally, tritium storage is discussed regarding tritium devices associated to Fusion Reactors and regarding smaller devices [fr

  6. An Ideal Gas Law Simulator for Atmospheric Gas Molecules ...

    African Journals Online (AJOL)

    The ideal gas law which is the equation of state of a hypothetical ideal gas that allows us to gain useful insights into the behavior of most real gases at low densities was utilized in this work to conceptualize, design and develop the ideal gas law simulator in a 3 dimensional space using Microsoft Visual Studio, Microsoft ...

  7. Elimination of effect of α-particles in tritium gas monitor

    International Nuclear Information System (INIS)

    Matsumoto, Yuzuru; Asaoka, Koichi; Manako, Hiroaki; Kumabe, Isao

    1982-01-01

    In order to obtain the high sensitivity in a tritium monitor, a cancellation circuit for α-particles emitted by Rn in air was designed and constructed. The cancellation circuit consists of a differentiating circuit, discriminator, peak-hold circuit and difference amplifier. Pulsed signals induced by α-particles are separated from tritium #betta#-signals by the differentiating circuit and the discriminator. After being shaped by the peak-hold circuit with the same decay time constant as that of the initial α-signals, the α-signals are subtracted from the initial signals by the difference amplifier. The experimental test of this system was carried out, and it was confirmed that the elimination of the effect of α-particles was achieved successfully by the use of this cancellation circuit. (author)

  8. Production of ultrapure D-T gas by removal of molecular tritium by selective adsorption

    International Nuclear Information System (INIS)

    Maienschein, J.L.; Hudson, R.S.; Tsugawa, R.T.; Fearon, E.M.; Souers, P.C.; Collins, G.W.

    1992-01-01

    Production of molecular deuterium-tritium (D-T) with very low molecular tritium (T 2 ) is necessary for application as a nuclear spin polarized fuel. Selective adsorption of hydrogen isotopes on zeolites or alumina can provide the separation needed to produce D-T with very low T 2 . Use of an absorption column at 20-25 K offers low inventory, compact size, and rapid operation, in comparison with conventional separation techniques such as cryogenic distillation or thermal diffusion. In this paper, the authors discuss principles of absorption, and describe a calculational model of the absorption column and operational implications revealed by it. The authors show experimental proof-of-principle data for removal of T 2 from D-T with an adsorption column operated at 23 K

  9. Results of experimental study on detritiation of atmosphere in large space

    International Nuclear Information System (INIS)

    Kobayashi, Kazuhiro; Hayashi, Takumi; Iwai, Yasunori; Nishi, Masataka

    2001-01-01

    In order to obtain data on tritium removal from the atmosphere of a room, which is needed for designing a reliable effective atmosphere detritiation system in a fusion reactor and for detailed analysis on its safety, intentional tritium release experiments have been carried out in a controlled space called Caisson under various atmosphere conditions at the Tritium Process Laboratory (TPL) in Japan Atomic Energy Research Institute (JAERI). In case there is no tritiated water vapor in the released tritium gas, tritium was ideally removed by constant ventilation in spite of atmospheric conditions and residence time. On the other hand, when tritiated water vapor existed in the released tritium, residual contamination on the wall of the Caisson was detected and it was found that it depended on the initial humidity in the Caisson. This tritium removal behavior was successfully analyzed by considering the adsorption and desorption reaction rates of tritiated water on the wall by the constant ventilation

  10. Characterization of contaminated oil with tritium, from of production of gas tripolar scintillators

    International Nuclear Information System (INIS)

    Potiens Junior, Ademar J.; Marumo, Julio T.; Goes, Marcos M.; Isiki, Vera L.K.

    2001-01-01

    The objective of this work was to develop a methodology to estimate the activity level present in radioactive oil samples. This oil is derived from vacuum pumps used to produce tension protector of electronic equipment in telecommunication area. The method consisted in obtain a calibration curve in counts per minute versus tritium activity. After the equipment calibration it was analyzed 3 batches of radioactive oil samples. (author)

  11. Analysis of the tritium gas sample by gas chromatography. one of the basic steps in the fuel cycle of the ITER

    International Nuclear Information System (INIS)

    Szuecs, Z.

    2006-01-01

    Complete text of publication follows. The international consortium (EU, USA, Russia, Japan, South Korea, China and India) signed a formal agreement to build the International Thermonuclear Experimental Reactor (ITER) on November 21, 2006. The official objective of ITER is to 'demonstrate the scientific and technological feasibility of fusion energy for peaceful purposes'. The deuterium-tritium fusion process releases roughly three times much energy as uranium 235 fission and millions of times more energy than a chemical reaction such as the burning of coal or hydrocarbons. It is the goal of a fusion power plant to harness this energy to produce electricity. The Atomki recognized this perspective trend at time and it was involved into the fusion research by the Hungarian Fusion Association from September 2005. This short communication is referring about the cooperation, which was realized between the Atomki and the Tritium Laboratory Karlsruhe (TLK) in field of the analysis of the tritium gas samples from spring of 2006. The tritium is one of the main important fuel materials for the fusion reactor. As a radioactive gas it needs special attention for its handling and analysis. In the TLK has been developed gas-chromatographic technology for checking of the tritium gas sampling, origin from the different parts of the Tritium Plant. However this method is already 14 years old and the old staff was changed 2 years ago, loosed some important knowhow at the same time. Therefore was necessary to check the system and to carry out some important maintenance. All of them are summarized in the following 4 points: 1. The continuously increasing of the retention time of the Porapack Q column created the question: Nor the resin phase of the column already damaged or the resin works properly and any other effect (leak on the pipe system or in the valves or in pressure regulators, changing of the inlet and outlet pressure and the changing of the ratio of the flow rates) occurs

  12. Development of tritium technology at the Tritium Systems Test Assembly

    International Nuclear Information System (INIS)

    Anderson, J.L.; Bartlit, J.R.

    1982-01-01

    The Tritium Systems Test Assembly (TSTA) at the Los Alamos National Laboratory is dedicated to the development, demonstration, and interfacing of technologies related to the deuterium-tritium fuel cycle for large scale fusion reactor systems starting with the Fusion Engineering Device (FED) or the International Tokamak Reactor (INTOR). This paper briefly describes the fuel cycle and safety systems at TSTA including the Vacuum Facility, Fuel Cleanup, Isotope Separation, Transfer Pumping, Emergency Tritium Cleanup, Tritium Waste Treatment, Tritium Monitoring, Data Acquisition and Control, Emergency Power and Gas Analysis systems. Discussed in further detail is the experimental program proposed for the startup and testing of these systems

  13. ACUTRI a computer code for assessing doses to the general public due to acute tritium releases

    CERN Document Server

    Yokoyama, S; Noguchi, H; Ryufuku, S; Sasaki, T

    2002-01-01

    Tritium, which is used as a fuel of a D-T burning fusion reactor, is the most important radionuclide for the safety assessment of a nuclear fusion experimental reactor such as ITER. Thus, a computer code, ACUTRI, which calculates the radiological impact of tritium released accidentally to the atmosphere, has been developed, aiming to be of use in a discussion of licensing of a fusion experimental reactor and an environmental safety evaluation method in Japan. ACUTRI calculates an individual tritium dose based on transfer models specific to tritium in the environment and ICRP dose models. In this calculation it is also possible to analyze statistically on meteorology in the same way as a conventional dose assessment method according to the meteorological guide of the Nuclear Safety Commission of Japan. A Gaussian plume model is used for calculating the atmospheric dispersion of tritium gas (HT) and/or tritiated water (HTO). The environmental pathway model in ACUTRI considers the following internal exposures: i...

  14. Tritium waste package

    Science.gov (United States)

    Rossmassler, Rich; Ciebiera, Lloyd; Tulipano, Francis J.; Vinson, Sylvester; Walters, R. Thomas

    1995-01-01

    A containment and waste package system for processing and shipping tritium xide waste received from a process gas includes an outer drum and an inner drum containing a disposable molecular sieve bed (DMSB) seated within outer drum. The DMSB includes an inlet diffuser assembly, an outlet diffuser assembly, and a hydrogen catalytic recombiner. The DMSB absorbs tritium oxide from the process gas and converts it to a solid form so that the tritium is contained during shipment to a disposal site. The DMSB is filled with type 4A molecular sieve pellets capable of adsorbing up to 1000 curies of tritium. The recombiner contains a sufficient amount of catalyst to cause any hydrogen add oxygen present in the process gas to recombine to form water vapor, which is then adsorbed onto the DMSB.

  15. The organically bound tritium: an analyst vision

    International Nuclear Information System (INIS)

    Ansoborlo, E.; Baglan, N.

    2009-01-01

    The authors report the work of a work group on tritium analysis. They recall the different physical forms of tritium: gas (HT, hydrogen-tritium), water vapour (HTO or tritiated water) or methane (CH3T), but also in organic compounds (OBT, organically bound tritium) which are either exchangeable or non-exchangeable. They evoke measurement techniques and methods, notably to determine the tritium volume activity. They discuss the possibilities to analyse and distinguish exchangeable and non-exchangeable OBTs

  16. Monitoring of tritium

    Science.gov (United States)

    Corbett, James A.; Meacham, Sterling A.

    1981-01-01

    The fluid from a breeder nuclear reactor, which may be the sodium cooling fluid or the helium reactor-cover-gas, or the helium coolant of a gas-cooled reactor passes over the portion of the enclosure of a gaseous discharge device which is permeable to hydrogen and its isotopes. The tritium diffused into the discharge device is radioactive producing beta rays which ionize the gas (argon) in the discharge device. The tritium is monitored by measuring the ionization current produced when the sodium phase and the gas phase of the hydrogen isotopes within the enclosure are in equilibrium.

  17. Tritium transport calculations for the IFMIF Tritium Release Test Module

    Energy Technology Data Exchange (ETDEWEB)

    Freund, Jana, E-mail: jana.freund@kit.edu; Arbeiter, Frederik; Abou-Sena, Ali; Franza, Fabrizio; Kondo, Keitaro

    2014-10-15

    Highlights: • Delivery of material data for the tritium balance in the IFMIF Tritium Release Test Module. • Description of the topological models in TMAP and the adapted fusion-devoted Tritium Permeation Code (FUS-TPC). • Computation of release of tritium from the breeder solid material into the purge gas. • Computation of the loss of tritium over the capsule wall, rig hull, container wall and purge gas return line. - Abstract: The IFMIF Tritium Release Test Module (TRTM) is projected to measure online the tritium release from breeder ceramics and beryllium pebble beds under high energy neutron irradiation. Tritium produced in the pebble bed of TRTM is swept out continuously by a purge gas flow, but can also permeate into the module's metal structures, and can be lost by permeation to the environment. According analyses on the tritium inventory are performed to support IFMIF plant safety studies, and to support the experiment planning. This paper describes the necessary elements for calculation of the tritium transport in the Tritium Release Test Module as follows: (i) applied equations for the tritium balance, (ii) material data from literature and (iii) the topological models and the computation of the five different cases; namely release of tritium from the breeder solid material into the purge gas, loss of tritium over the capsule wall, rig hull, container wall and purge gas return line in detail. The problem of tritium transport in the TRTM has been studied and analyzed by the Tritium Migration Analysis Program (TMAP) and the adapted fusion-devoted Tritium Permeation Code (FUS-TPC). TMAP has been developed at INEEL and now exists in Version 7. FUS-TPC Code was written in MATLAB with the original purpose to study the tritium transport in Helium Cooled Lead Lithium (HCLL) blanket and in a later version the Helium Cooled Pebble Bed (HCPB) blanket by [6] (Franza, 2012). This code has been further modified to be applicable to the TRTM. Results from the

  18. Tritium transport calculations for the IFMIF Tritium Release Test Module

    International Nuclear Information System (INIS)

    Freund, Jana; Arbeiter, Frederik; Abou-Sena, Ali; Franza, Fabrizio; Kondo, Keitaro

    2014-01-01

    Highlights: • Delivery of material data for the tritium balance in the IFMIF Tritium Release Test Module. • Description of the topological models in TMAP and the adapted fusion-devoted Tritium Permeation Code (FUS-TPC). • Computation of release of tritium from the breeder solid material into the purge gas. • Computation of the loss of tritium over the capsule wall, rig hull, container wall and purge gas return line. - Abstract: The IFMIF Tritium Release Test Module (TRTM) is projected to measure online the tritium release from breeder ceramics and beryllium pebble beds under high energy neutron irradiation. Tritium produced in the pebble bed of TRTM is swept out continuously by a purge gas flow, but can also permeate into the module's metal structures, and can be lost by permeation to the environment. According analyses on the tritium inventory are performed to support IFMIF plant safety studies, and to support the experiment planning. This paper describes the necessary elements for calculation of the tritium transport in the Tritium Release Test Module as follows: (i) applied equations for the tritium balance, (ii) material data from literature and (iii) the topological models and the computation of the five different cases; namely release of tritium from the breeder solid material into the purge gas, loss of tritium over the capsule wall, rig hull, container wall and purge gas return line in detail. The problem of tritium transport in the TRTM has been studied and analyzed by the Tritium Migration Analysis Program (TMAP) and the adapted fusion-devoted Tritium Permeation Code (FUS-TPC). TMAP has been developed at INEEL and now exists in Version 7. FUS-TPC Code was written in MATLAB with the original purpose to study the tritium transport in Helium Cooled Lead Lithium (HCLL) blanket and in a later version the Helium Cooled Pebble Bed (HCPB) blanket by [6] (Franza, 2012). This code has been further modified to be applicable to the TRTM. Results from the

  19. Use of tritium and sources

    International Nuclear Information System (INIS)

    Noguchi, Hiroshi

    1997-01-01

    There are many kinds of tritium, sources in the environment. The maximum inventory of them is the nuclear tests, although the atmospheric nuclear test has not been carried out since 1981. So that the inventory originated from them will decrease. By the latest data in 1989, the total amount of released tritium was about 24 PBq/yr by the use of atomic energy in the world. The maximum source was the heavy water moderated reactors, for example, CANDU reactor. In the future, large amount of tritium inventory may be the fusion reactor. The test of JET (Joint European Torus) released about 600 GBq of tritium until March in 1992. 80-90% of them were tritium water (HTO). The amount of tritium released from industries and medicine are limited. Although ITER has a large amount of tritium inventory, the amount of release is seemed not to be larger than other nuclear power facility. (S.Y.)

  20. Tritium Sequestration in Gen IV NGNP Gas Stream via Proton Conducting Ceramic Pumps

    Energy Technology Data Exchange (ETDEWEB)

    Chen, Fanglin Frank [Univ. of South Carolina, Columbia, SC (United States); Adams, Thad M. [Savannah River Site (SRS), Aiken, SC (United States). Savannah River National Lab. (SRNL); Brinkman, Kyle [Savannah River Site (SRS), Aiken, SC (United States). Savannah River National Lab. (SRNL); Reifsnider, Kenneth [Univ. of South Carolina, Columbia, SC (United States)

    2011-09-30

    Several types of high-temperature proton conductors based on SrCeO3 and BaCeO3 have been systematically investigated in this project for tritium separation in NGNP applications. One obstacle for the field application is the chemical stability issues in the presence of steam and CO2 for these proton conductors. Several strategies to overcome such issues have been evaluated, including A site doping and B site co-doping method for perovskite-structured proton conductors. Novel zirconium-free proton conductors have also been developed with improved electrical conductivity and enhanced chemical stability. Novel catalytic materials for the proton-conducting separation membranes have been investigated. A tubular geometry proton-conducting membrane has been developed for the proton separation membranes. Total dose rate estimated from tritium decay (beta emission) under realistic membrane operating conditions, combined with electron irradiation experiments, indicates that proton ceramic materials possess the appropriate radiation stability for this application.

  1. Overview of the tritium system of Ignitor

    International Nuclear Information System (INIS)

    Rizzello, C.; Tosti, S.

    2008-01-01

    Among the recent design activities of the Ignitor program, the analysis of the tritium system has been carried out with the aim to describe the main equipments and the operations needed for supplying the deuterium-tritium mixtures and recovering the plasma exhaust. In fact, the tritium system of Ignitor provides for injecting deuterium-tritium mixtures into the vacuum chamber in order to sustain the fusion reaction: furthermore, it generally manages and controls the tritium and the tritiated materials of the machine fuel cycle. Main functions consist of tritium storage and delivery, tritium injection, tritium recovery from plasma exhaust, treatment of the tritiated wastes, detritiation of the contaminated atmospheres, tritium analysis and accountability. In this work an analysis of the designed tritium system of Ignitor is summarized

  2. Dense gas dispersion in the atmosphere

    Energy Technology Data Exchange (ETDEWEB)

    Nielsen, Morten

    1998-09-01

    Dense gas dispersion is characterized by buoyancy induced gravity currents and reduction of the vertical mixing. Liquefied gas releases from industrial accidents are cold because of the heat of evaporation which determines the density for a given concentration and physical properties. The temperature deficit is moderated by the heat flux from the ground, and this convection is an additional source of turbulence which affects the mixing. A simple model as the soil heat flux is used to estimate the ability of the ground to sustain the heat flux during release. The initial enthalpy, release rate, initial entrainment and momentum are discussed for generic source types and the interaction with obstacles is considered. In the MTH project BA experiments source with and without momentum were applied. The continuously released propane gas passed a two-dimensional removable obstacle perpendicular to the wind direction. Ground-level gas concentrations and vertical profiles of concentration, temperature, wind speed and turbulence were measured in front of and behind the obstacle. Ultrasonic anemometers providing fast velocity and concentration signals were mounted at three levels on the masts. The observed turbulence was influenced by the stability and the initial momentum of the jet releases. Additional information were taken from the `Dessert tortoise` ammonia jet releases, from the `Fladis` experiment with transition from dense to passive dispersion, and from the `Thorney Island` continuous releases of isothermal freon mixtures. The heat flux was found to moderate the negative buoyancy in both the propane and ammonia experiments. The heat flux measurements are compared to an estimate by analogy with surface layer theory. (au) 41 tabs., 146 ills., 189 refs.

  3. Modelling the environmental transport of tritium in the vicinity of long term atmospheric and sub-surface sources. Report of the Tritium Working Group of the Biosphere Modelling and Assessment (BIOMASS) Programme, Theme 3

    International Nuclear Information System (INIS)

    2003-03-01

    The IAEA Programme on BIOsphere Modelling and ASSessment (BIOMASS) was launched in Vienna in October 1996. The programme was concerned with developing and improving capabilities to predict the transfer of radionuclides in the environment. The programme had three themes: Theme 1: Radioactive Waste Disposal. The objective was to develop the concept of a standard or reference biosphere for application to the assessment of the long term safety of repositories for radioactive waste. Theme 2: Environmental Releases. BIOMASS provided an international forum for activities aimed at increasing the confidence in methods and models for the assessment of radiation exposure related to environmental releases. Two Working Groups addressed issues concerned with the reconstruction of radiation doses received by people from past releases of radionuclides to the environment and the evaluation of the efficacy of remedial measures. Theme 3: Biosphere Processes. The aim of this Theme was to improve capabilities for modelling the transfer of radionuclides in particular parts of the biosphere identified as being of potential radiological significance and where there were gaps in modelling approaches. This topic was explored using a range of methods including reviews of the literature, model inter-comparison exercises and, where possible, model testing against independent sources of data. Three Working Groups were established to examine the modelling of: (1) long term tritium dispersion in the environment; (2) radionuclide uptake by fruits; and (3) radionuclide migration and accumulation in forest ecosystems. This report describes results of the studies undertaken by the Tritium Working Group under Theme 3. It discusses the six model test exercises (three model-model intercomparisons and three model-data exercises) and the twenty-month field sampling programme undertaken to investigate the environmental transport of tritium in the vicinity of long term atmospheric and sub-surface sources

  4. Tritium dynamics in soils and plants at a tritium processing facility in Canada

    Energy Technology Data Exchange (ETDEWEB)

    Mihok, S.; St-Amanat, N.; Kwamena, N.O. [Canadian Nuclear Safety Commission (Canada); Clark, I.; Wilk, M.; Lapp, A. [University of Ottawa (Canada)

    2014-07-01

    The dynamics of tritium released as tritiated water (HTO) have been studied extensively with results incorporated into environmental models such as CSA N288.1 used for regulatory purposes in Canada. The dispersion of tritiated gas (HT) and rates of oxidation to HTO have been studied under controlled conditions, but there are few studies under natural conditions. HT is a major component of the tritium released from a gaseous tritium light manufacturing facility in Canada (CNSC INFO-0798). To support the improvement of models, a garden was set up in one summer near this facility in a spot with tritium in air averaging ∼ 5 Bq/m{sup 3} HTO (passive diffusion monitors). Atmospheric stack releases (575 GBq/week) were recorded weekly. HT releases occur mainly during working hours with an HT:HTO ratio of 2.6 as measured at the stack. Soils and plants (leaves/stems and roots/tubers) were sampled for HTO and organically-bound tritium (OBT) weekly. Active day-night monitoring of air was conducted to interpret tritium dynamics relative to weather and solar radiation. The experimental design included a plot of natural grass/soil, contrasted with grass (sod) and Swiss chard, pole beans and potatoes grown in barrels under different irrigation regimes (in local topsoil at 29 Bq/L HTO, 105 Bq/L OBT). All treatments were exposed to rain (80 Bq/L) and atmospheric releases of tritium (weekdays), and reflux of tritium from soils (initial conditions of 284 Bq/L HTO, 3,644 Bq/L OBT) from 20 years of operations. Three irrigation regimes were used for barrel plants to mimic home garden management: rain only, low tritium tap water (5 Bq/L), and high tritium well water (mean 10,013 Bq/L). This design provided a range of plants and starting conditions with contrasts in initial HTO/OBT activity in soils, and major tritium inputs from air versus water. Controls were two home gardens far from any tritium sources. Active air monitoring indicated that the plume was only occasionally present for

  5. Tritium monitor and collection system

    Science.gov (United States)

    Bourne, G.L.; Meikrantz, D.H.; Ely, W.E.; Tuggle, D.G.; Grafwallner, E.G.; Wickham, K.L.; Maltrud, H.R.; Baker, J.D.

    1992-01-14

    This system measures tritium on-line and collects tritium from a flowing inert gas stream. It separates the tritium from other non-hydrogen isotope contaminating gases, whether radioactive or not. The collecting portion of the system is constructed of various zirconium alloys called getters. These alloys adsorb tritium in any of its forms at one temperature and at a higher temperature release it as a gas. The system consists of four on-line getters and heaters, two ion chamber detectors, two collection getters, and two guard getters. When the incoming gas stream is valved through the on-line getters, 99.9% of it is adsorbed and the remainder continues to the guard getter where traces of tritium not collected earlier are adsorbed. The inert gas stream then exits the system to the decay chamber. Once the on-line getter has collected tritium for a predetermined time, it is valved off and the next on-line getter is valved on. Simultaneously, the first getter is heated and a pure helium purge is employed to carry the tritium from the getter. The tritium loaded gas stream is then routed through an ion chamber which measures the tritium activity. The ion chamber effluent passes through a collection getter that readsorbs the tritium and is removable from the system once it is loaded and is then replaced with a clean getter. Prior to removal of the collection getter, the system switches to a parallel collection getter. The effluent from the collection getter passes through a guard getter to remove traces of tritium prior to exiting the system. The tritium loaded collection getter, once removed, is analyzed by liquid scintillation techniques. The entire sequence is under computer control except for the removal and analysis of the collection getter. 7 figs.

  6. Release of gaseous tritium during reprocessing

    International Nuclear Information System (INIS)

    Bruecher, H.; Hartmann, K.

    1983-01-01

    About 50% of the tritium put through an LWR reprocessing plant is obtained as tritium-bearing water, HTO. Gaseous tritium, HT has a radiotoxicity which is by 4 orders of magnitude lower than that of HTO. A possibility for the removal of HTO could therefore be its conversion into the gas phase with subsequent emission of the HT into the atmosphere. However, model computations which are, in part, supported by experimental data reveal that the radiation exposure caused by HT release is only by about one order of magnitude below that caused by HTO. This is being attributed to the relatively quick reoxidation of HT by soil bacteria. Two alternatives for producing HT from HTO (electrolysis; voloxidation with subsequent electrolysis) are presented and compared with the reference process of deep-well injection of HTO. The authors come to the conclusion that tritium removal by HT release into the atmosphere cannot be recommended at present under either radiological or economic aspects. (orig.) [de

  7. Tritium monitor with improved gamma-ray discrimination

    Science.gov (United States)

    Cox, Samson A.; Bennett, Edgar F.; Yule, Thomas J.

    1985-01-01

    Apparatus and method for selective measurement of tritium oxide in an environment which may include other radioactive components and gamma radiation, the measurement including the selective separation of tritium oxide from a sample gas through a membrane into a counting gas, the generation of electrical pulses individually representative by rise times of tritium oxide and other radioactivity in the counting gas, separation of the pulses by rise times, and counting of those pulses representative of tritium oxide. The invention further includes the separate measurement of any tritium in the sample gas by oxidizing the tritium to tritium oxide and carrying out a second separation and analysis procedure as described above.

  8. Arc melting in inert gas atmosphere of zirconium sponge

    International Nuclear Information System (INIS)

    Julio Junior, O.; Andrade, A.H.P. de

    1991-01-01

    The obtainment of metallic zirconium in laboratory scale with commercial and nuclear quality is the objective of the Metallurgy Department of IEN/CNEN - Brazil, so a melting procedure of zirconium sponge in laboratory scale using an arc furnace in inert atmosphere is developed. The effects of atmosphere operation, and the use of gas absorber and the sponge characteristics over the quality of button in as-cast reporting with hardness measures are described. (C.G.C.)

  9. Gas exchange between the forest and the atmosphere

    International Nuclear Information System (INIS)

    Murphy, C.E. Jr.

    1985-01-01

    Forest gas exchange is discussed in terms of the processes that control the rate of exchange with the atmosphere. Examples are presented to show how vegetative uptake control is varied for gases with different characteristics. The prediction of uptake for large areas and over long periods of time is discussed in terms of quantitative models of the gas exchange processes. Finally, remote sensing is suggested as a means of obtaining the parameters needed to make the model predictions. 46 refs., 6 figs

  10. Tritium practices past and present

    International Nuclear Information System (INIS)

    Gede, V.P.; Gildea, P.D.

    1980-01-01

    History of the production and use of tritium, as well as handling techniques, are reviewed. Handling techniques first used at Lawrence Livermore National Laboratory made use of glass vacuum systems and relatively crude ion chambers for monitoring airborne activity. The first use of inert atmosphere glove boxes demonstrated that uptake through the skin could be a serious personnel exposure problem. Growing environmental concerns in the early 1970's resulted in the implementation by the Atomic Energy Commission of a new criteria to limit atmospheric tritium releases to levels as low as practicable. An important result of the new criteria was the development of containment and recovery systems to capture tritium rather than vent it to the atmosphere. The Sandia National Laboratories, Livermore, Tritium Research Laboratory containment and decontamination systems are presented as a typical example of this technology. The application of computers to control systems is expected to provide the greatest potential for change in future tritium handling practices

  11. Tritium concentrations in tree ring cellulose

    International Nuclear Information System (INIS)

    Kaji, Toshio; Momoshima, Noriyuki; Takashima, Yoshimasa.

    1989-01-01

    Measurements of tritium (tissue bound tritium; TBT) concentration in tree rings are presented and discussed. Such measurement is expected to provide a useful means of estimating the tritium level in the environment in the past. The concentration of tritium bound in the tissue (TBT) in a tree ring considered to reflect the environmental tritium level in the area at the time of the formation of the ring, while the concentration of tritium in the free water in the tissue represents the current environmental tritium level. First, tritium concentration in tree ring cellulose sampled from a cedar tree grown in a typical environment in Fukuoka Prefecture is compared with the tritium concentration in precipitation in Tokyo. Results show that the year-to-year variations in the tritium concentration in the tree rings agree well with those in precipitation. The maximum concentration, which occurred in 1963, is attibuted to atmospheric nuclear testing which was performed frequently during the 1961 - 1963 period. Measurement is also made of the tritium concentration in tree ring cellulose sampled from a pine tree grown near the Isotope Center of Kyushu University (Fukuoka). Results indicate that the background level is higher probably due to the release of tritium from the facilities around the pine tree. Thus, measurement of tritium in tree ring cellulose clearly shows the year-to-year variation in the tritium concentration in the atmosphere. (N.K.)

  12. Noble gas atmospheric monitoring at reprocessing facilities

    International Nuclear Information System (INIS)

    Nakhleh, C.W.; Perry, R.T. Jr.; Poths, J.; Stanbro, W.D.; Wilson, W.B.; Fearey, B.L.

    1997-01-01

    The discovery in Iraq after the Gulf War of the existence of a large clandestine nuclear-weapon program has led to an across-the-board international effort, dubbed Programme 93+2, to improve the effectiveness and efficiency of International Atomic Energy Agency (IAEA) safeguards. One particularly significant potential change is the introduction of environmental monitoring (EM) techniques as an adjunct to traditional safeguards methods. Monitoring of stable noble gas (Kr, Xe) isotopic abundances at reprocessing plant stacks appears to be able to yield information on the burnup and type of the fuel being processed. To estimate the size of these signals, model calculations of the production of stable Kr, Xe nuclides in reactor fuel and the subsequent dilution of these nuclides in the plant stack are carried out for two case studies: reprocessing of PWR fuel with a burnup of 35 GWd/tU, and reprocessing of CAND fuel with a burnup of 1 GWd/tU. For each case, a maximum-likelihood analysis is used to determine the fuel burnup and type from the isotopic data

  13. Basic characteristics of hollow-filament polyimide membrane in gas separation and application to tritium monitors

    International Nuclear Information System (INIS)

    Sasaki, Sh.; Suzuki, T.; Kondo, K.; Tega, E.; Shimada, A.; Akahori, S.; Okuno, K.

    2003-01-01

    The separation efficiency of hollow-filament polyimide membranes for 3 H and 41 Ar is preliminarily examined for a potential application to continuous gas monitoring systems for analysis of stack emission from accelerator facilities. The basic gas separation characteristics of the membranes are experimentally investigated, and a preliminary gas monitor design is proposed. The membranes are capable of selectively enriching hydrogen by more than 25 times, with negligible variation with respect to the species of isotope. (author)

  14. Atmospheric pressure helium afterglow discharge detector for gas chromatography

    Science.gov (United States)

    Rice, Gary; D'Silva, Arthur P.; Fassel, Velmer A.

    1986-05-06

    An apparatus for providing a simple, low-frequency electrodeless discharge system for atmospheric pressure afterglow generation. A single quartz tube through which a gas mixture is passed is extended beyond a concentric electrode positioned thereabout. A grounding rod is placed directly above the tube outlet to permit optical viewing of the discharge between the electrodes.

  15. Tritium containment of controlled thermonuclear fusion reactor

    International Nuclear Information System (INIS)

    Tanaka, Yoshihisa; Tsukumo, Kiyohiko; Suzuki, Tatsushi

    1979-01-01

    It is well known that tritium is used as the fuel for nuclear fusion reactors. The neutrons produced by the nuclear fusion reaction of deuterium and tritium react with lithium in blankets, and tritium is produced. The blankets reproduce the tritium consumed in the D-T reaction. Tritium circulates through the main cooling system and the fuel supply and evacuation system, and is accumulated. Tritium is a radioactive substance emitting β-ray with 12.6 year half-life, and harmful to human bodies. It is an isotope of hydrogen, and apt to diffuse and leak. Especially at high temperature, it permeates through materials, therefore it is important to evaluate the release of tritium into environment, to treat leaked tritium to reduce its release, and to select the method of containing tritium. The permeability of tritium and its solubility in structural materials are discussed. The typical blanket-cooling systems of nuclear fusion reactors are shown, and the tungsten coating of steam generator tubes and tritium recovery system are adopted for reducing tritium leak. In case of the Tokamak type reactor of JAERI, the tritium recovery system is installed, in which the tritium gas produced in blankets is converted to tritium steam with a Pd-Pt catalytic oxidation tower, and it is dehydrated and eliminated with a molecular sieve tower, then purified and recovered. (Kako, I.)

  16. Tritium in the aquatic environment

    International Nuclear Information System (INIS)

    Blaylock, B.G.; Hoffman, F.O.; Frank, M.L.

    1986-02-01

    Tritium is of environmental importance because it is released from nuclear facilities in relatively large quantities and because it has a half life of 12.26 y. Most of the tritium released into the atmosphere eventually reaches the aqueous environment, where it is rapidly taken up by aquatic organisms. This paper reviews the current literature on tritium in the aquatic environment. Conclusions from the review, which covered studies of algae, aquatic macrophytes, invertebrates, fish, and the food chain, were that aquatic organisms incorporate tritium into their tissue-free water very rapidly and reach concentrations near those of the external medium. The rate at which tritium from tritiated water is incorporated into the organic matter of cells is slower than the rate of its incorporation into the tissue-free water. If organisms consume tritiated food, incorporation of tritium into the organic matter is faster, and a higher tritium concentration is reached than when the organisms are exposed to only tritiated water alone. Incorporation of tritium bound to molecules into the organic matter depends on the chemical form of the ''carrier'' molecule. No evidence was found that biomagnification of tritium occurs at higher trophic levels. Radiation doses from tritium releases to large populations of humans will most likely come from the consumption of contaminated water rather than contaminated aquatic food products

  17. Tritium. Today's and tomorrow's developments

    International Nuclear Information System (INIS)

    Gazal, S.; Amiard, J.C.; Caussade, Bernard; Chenal, Christian; Hubert, Francoise; Sene, Monique

    2010-01-01

    Radioactive hydrogen isotope, tritium is one of the radionuclides which is the most released in the environment during the normal operation of nuclear facilities. The increase of nuclear activities and the development of future generations of reactors, like the EPR and ITER, would lead to a significant increase of tritium effluents in the atmosphere and in the natural waters, thus raising many worries and questions. Aware about the importance of this question, the national association of local information commissions (ANCLI) wished to make a status of the existing knowledge concerning tritium and organized in 2008 a colloquium at Orsay (France) with an inquiring approach. The scientific committee of the ANCLI, renowned for its expertise skills, mobilized several nuclear specialists to carry out this thought. This book represents a comprehensive synthesis of today's knowledge about tritium, about its management and about its impact on the environment and on human health. Based on recent scientific data and on precise examples, it treats of the overall questions raised by this radionuclide: 1 - tritium properties and different sources (natural and anthropic), 2 - the problem of tritiated wastes management; 3 - the bio-availability and bio-kinetics of the different tritium species; 4 - the tritium labelling of environments; 5 - tritium measurement and modeling of its environmental circulation; 6 - tritium radio-toxicity and its biological and health impacts; 7 - the different French and/or international regulations concerning tritium. (J.S.)

  18. Mass transfer behavior of tritium from air to water through the water surface

    International Nuclear Information System (INIS)

    Takata, Hiroki; Nishikawa, Masabumi; Kamimae, Kozo

    2005-01-01

    It is anticipated that a certain amount of tritiated water exists in the atmosphere of tritium handling facilities, and it is recognized that the hazardous potential of tritiated water is rather high. Then, it is important to grasp the behavior of tritiated water for preserving of the radiation safety. The mass transfer behavior of tritium from air to water through the water surface was discussed in this study. The evaporation rate of water and the condensation rate of water were experimentally examined from measurement of change of the weight of distilled water. The tritium transfer rate from the tritiated water in air to the distilled water was also experimentally examined by using a liquid scintillation counter. Experimental results about change of tritium level in a small beaker placed in the atmosphere with tritiated water showed that diffusion of tritium in water and gas flow in the atmosphere gives considerable effect on tritium transfer. The estimation method of the tritium transfer made in this study was applied to explain the data at The Japan Atomic Power Company second power station at Tsuruga and good agreement was obtained. (author)

  19. Evaluation of Ruthenium Capture Methods for Tritium Pretreatment Off-Gas Streams

    Energy Technology Data Exchange (ETDEWEB)

    Spencer, Barry B. [Oak Ridge National Lab. (ORNL), Oak Ridge, TN (United States); Jubin, Robert Thomas [Oak Ridge National Lab. (ORNL), Oak Ridge, TN (United States); Bruffey, Stephanie H. [Oak Ridge National Lab. (ORNL), Oak Ridge, TN (United States); Strachan, Denis M. [Oak Ridge National Lab. (ORNL), Oak Ridge, TN (United States)

    2017-07-01

    In the reprocessing of used nuclear fuel, radioactive elements are released into various plant off-gas streams. While much research and development has focused on the abatement of the volatile nuclides 3H, 14C, 85Kr, and 129I, the potential release of semivolatile isotopes that could also report to the off-gas streams in a reprocessing facility has been examined. Ruthenium (as 106Ru) has been identified as one of the semivolatile nuclides requiring the greatest degree of abatement prior to discharging the plant off-gas to the environment.

  20. Study and application of hydrophobic catalyst in treating tritium waste

    International Nuclear Information System (INIS)

    Dan, Gui-ping; Zhang, Dong; Qiu, Yong-mei; Yuan, Guo-Qi

    2008-01-01

    Tritium decontamination from tritium waste is important for the management of tritium waste. Tritium removal from waste tritium oxide can not only get tritium, but also reduce the amount of waste tritium. At the meantime, by cleaning the tritium pollution gas can also reduce the tritium exhausting from tritium facility. At present, the process of hydrogen isotopic exchange in tritium removal from waste tritium oxide and coordination oxidisation-adsorption in tritium cleaning from waste tritium gas are the mainly methods. In these methods, hydrophobic catalysts which can be used in these process are the key technology. There are many references about their preparing and applying, but few on the estimation about their performance changing during their applying. However, their performance stability on isotopic catalytic exchange and catalytic oxidisation will affect their using in reaction. Hydrophobic catalyst Pt-SDB which can be used in tritium isotopic exchange between tritium oxide and hydrogen and the cleaning of tritium pollution gas have been prepared in our laboratory in early days. In order to estimating their performance stability during their using, this work will investigate their stability on their catalytic activity and their radiation-resistance tritium. (author)

  1. Efficient gas exchange between a boreal river and the atmosphere

    Science.gov (United States)

    Huotari, Jussi; Haapanala, Sami; Pumpanen, Jukka; Vesala, Timo; Ojala, Anne

    2013-11-01

    largest uncertainties in accurately resolving the role of rivers and streams in carbon cycling stem from difficulties in determining gas exchange between water and the atmosphere. So far, estimates for river-atmosphere gas exchange have lacked direct ecosystem-scale flux measurements not disturbing gas exchange across the air-water interface. We conducted the first direct riverine gas exchange measurements with eddy covariance in tandem with continuous surface water CO2 measurements in a large boreal river for 30 days. Our measured gas transfer velocity was, on average, 20.8 cm h-1, which is clearly higher than the model estimates based on river channel morphology and water velocity, whereas our floating chambers gave comparable values at 17.3 cm h-1. These results demonstrate that present estimates for riverine CO2 emissions are very likely too low. This result is also relevant to any other gases emitted, as their diffusive exchange rates are similarly proportional to gas transfer velocity.

  2. Tritium oxidation and exchange: preliminary studies

    International Nuclear Information System (INIS)

    Phillips, J.E.; Easterly, C.E.

    1978-05-01

    The radiological hazard resulting from an exposure to either tritium oxide or tritium gas is discussed and the factors contributing to the hazard are presented. From the discussion it appears that an exposure to tritium oxide vapor is 10 4 to 10 5 times more hazardous than exposure to tritium gas. Present and future sources of tritium are briefly considered and indicate that most of the tritium has been and is being released as tritium oxide. The likelihood of gaseous releases, however, is expected to increase in the future, calling to task the present general release assumption that 100% of all tritium released is as oxide. Accurate evaluation of the hazards from a gaseous release will require a knowledge of the conversion rate of tritium gas to tritium oxide. An experiment for determining the conversion rate of tritium gas to tritium oxide is presented along with some preliminary data. The conversion rates obtained for low initial concentrations (10 -4 to 10 -1 mCi/ml) indicate the conversion may proceed more rapidly than would be expected from an extrapolation of previous data taken at higher concentrations

  3. Bioassay guideline 2: guidelines for tritium bioassay

    International Nuclear Information System (INIS)

    1983-01-01

    This guideline is one of a series under preparation by the Federal-Provincial Working Group on Bioassay and In Vivo Monitoring Criteria. In this report tritium compounds have been grouped into four categories for the purpose of calculating Annual Limits on Intake and Investigation Levels: tritium gas, tritiated water, tritium-labelled compounds and nucleic acid precursors

  4. Tritium analysis at TFTR

    International Nuclear Information System (INIS)

    Voorhees, D.R.; Rossmassler, R.L.; Zimmer, G.

    1995-01-01

    The tritium analytical system at TFRR is used to determine the purity of tritium bearing gas streams in order to provide inventory and accountability measurements. The system includes a quadrupole mass spectrometer and beta scintillator originally configured at Monsanto Mound Research Laboratory in the late 1970's and early 1980's. The system was commissioned and tested between 1991 and 1992 and is used daily for analysis of calibration standards, incoming tritium shipments, gases evolved from uranium storage beds and measurement of gases returned to gas holding tanks. The low resolution mass spectrometer is enhanced by the use of a metal getter pump to aid in resolving the mass 3 and 4 species. The beta scintillator complements the analysis as it detects tritium bearing species that often are not easily detected by mass spectrometry such as condensable species or hydrocarbons containing tritium. The instruments are controlled by a personal computer with customized software written with a graphical programming system designed for data acquisition and control. A discussion of the instrumentation, control systems, system parameters, procedural methods, algorithms, and operational issues will be presented. Measurements of gas holding tanks and tritiated water waste streams using ion chamber instrumentation are discussed elsewhere

  5. Tritium sources

    International Nuclear Information System (INIS)

    Glodic, S.; Boreli, F.

    1993-01-01

    Tritium is the only radioactive isotope of hydrogen. It directly follows the metabolism of water and it can be bound into genetic material, so it is very important to control levels of contamination. In order to define the state of contamination it is necessary to establish 'zero level', i.e. actual global inventory. The importance of tritium contamination monitoring increases with the development of fusion power installations. Different sources of tritium are analyzed and summarized in this paper. (author)

  6. Tritium storage

    International Nuclear Information System (INIS)

    Hircq, B.

    1989-01-01

    A general synthesis about tritium storage is achieved in this paper and a particular attention is given to practical application in the Fusion Technology Program. Tritium, storage under gaseous form and solid form are discussed (characteristics, advantages, disadvantages and equipments). The way of tritium storage is then discussed and a choice established as a function of a logic which takes into account the main working parameters

  7. Pebble fabrication and tritium release properties of an advanced tritium breeder

    Energy Technology Data Exchange (ETDEWEB)

    Hoshino, Tsuyoshi, E-mail: hoshino.tsuyoshi@jaea.go.jp [Breeding Functional Materials Development Group, Department of Blanket Systems Research, Rokkasho Fusion Institute, Sector of Fusion Research and Development, Japan Atomic Energy Agency, 2-166 Obuch, Omotedate, Rokkasho-mura, Kamikita-gun, Aomori 039-3212 (Japan); Edao, Yuki [Tritium Technology Group, Department of Blanket Systems Research, Rokkasho Fusion Institute, Sector of Fusion Research and Development, Japan Atomic Energy Agency, 2-4 Shirakata, Shirane, Tokai-mura, Naka-gun, Ibaraki 319-1195 (Japan); Kawamura, Yoshinori [Blanket Technology Group, Department of Blanket Systems Research, Rokkasho Fusion Institute, Sector of Fusion Research and Development, Japan Atomic Energy Agency, 801-1 Mukoyama, Naka, Ibaraki 311-0193 (Japan); Ochiai, Kentaro [BA Project Coordination Group, Department of Fusion Power Systems Research, Rokkasho Fusion Institute, Sector of Fusion Research and Development, Japan Atomic Energy Agency, 2-166 Obuch, Omotedate, Rokkasho-mura, Kamikita-gun, Aomori 039-3212 (Japan)

    2016-11-01

    Highlights: • Li{sub 2}TiO{sub 3} with excess Li (Li{sub 2+x}TiO{sub 3+y}) pebble as an advanced tritium breeders was fabricated using emulsion method. • Grain size of Li{sub 2+x}TiO{sub 3+y} pebbles was controlled to be less than 5 μm. • Li{sub 2+x}TiO{sub 3+y} pebbles exhibited good tritium release properties similar to that of Li{sub 2}TiO{sub 3} pebbles. - Abstract: Li{sub 2}TiO{sub 3} with excess Li (Li{sub 2+x}TiO{sub 3+y}) has been developed as an advanced tritium breeder. With respect to the tritium release characteristics of the blanket, the optimum grain size after sintering was less than 5 μm. Therefore, an emulsion method was developed to fabricate pebbles with this target grain size. The predominant factor affecting grain growth was assumed to be the presence of binder in the gel particles; this remaining binder was hypothesized to react with the excess Li, thereby generating Li{sub 2}CO{sub 3}, which promotes grain growth. To inhibit the generation of Li{sub 2}CO{sub 3}, calcined Li{sub 2+x}TiO{sub 3+y} pebbles were sintered under vacuum and subsequently under a 1% H{sub 2}–He atmosphere. The average grain size of the sintered Li{sub 2+x}TiO{sub 3+y} pebbles was less than 5 μm. Furthermore, the tritium release properties of Li{sub 2+x}TiO{sub 3+y} pebbles were evaluated, and deuterium–tritium (DT) neutron irradiation experiments were performed at the Fusion Neutronics Source facility in the Japan Atomic Energy Agency. To remove the tritium produced by neutron irradiation, 1% H{sub 2}–He purge gas was passed through the Li{sub 2+x}TiO{sub 3+y} pebbles. The Li{sub 2+x}TiO{sub 3+y} pebbles exhibited good tritium release properties, similar to those of Li{sub 2}TiO{sub 3} pebbles. In particular, the released amount of tritiated hydrogen gas for easier tritium handling was greater than the released amount of tritiated water.

  8. Method of controlling weld chamber purge and cover gas atmosphere

    International Nuclear Information System (INIS)

    Yeo, D.

    1992-01-01

    A method of controlling the gas atmosphere in a welding chamber includes detecting the absence of a fuel rod from the welding chamber and, in response thereto, initiating the supplying of a flow of argon gas to the chamber to purge air therefrom. Further, the method includes detecting the entry of a fuel rod in the welding chamber and, in response thereto, terminating the supplying of the flow of argon gas to the chamber and initiating the supplying of a flow of helium gas to the chamber to purge argon gas therefrom and displace the argon gas in the chamber. Also, the method includes detecting the withdrawal of the fuel rod from the welding chamber and, in response thereto, terminating the supplying of the flow of helium gas to the chamber and initiating the supplying of argon to the chamber to purge the air therefrom. The method also includes detecting the initiation of a weld cycle and, in response thereto, momentarily supplying a flow of argon gas to the welding electrode tip for initiating the welding arc. (Author)

  9. Tritium module for ITER/Tiber system code

    International Nuclear Information System (INIS)

    Finn, P.A.; Willms, S.; Busigin, A.; Kalyanam, K.M.

    1988-01-01

    A tritium module was developed for the ITER/Tiber system code to provide information on capital costs, tritium inventory, power requirements and building volumes for these systems. In the tritium module, the main tritium subsystems/emdash/plasma processing, atmospheric cleanup, water cleanup, blanket processing/emdash/are each represented by simple scaleable algorithms. 6 refs., 2 tabs

  10. Silicon microring refractometric sensor for atmospheric CO(2) gas monitoring.

    Science.gov (United States)

    Mi, Guangcan; Horvath, Cameron; Aktary, Mirwais; Van, Vien

    2016-01-25

    We report a silicon photonic refractometric CO(2) gas sensor operating at room temperature and capable of detecting CO(2) gas at atmospheric concentrations. The sensor uses a novel functional material layer based on a guanidine polymer derivative, which is shown to exhibit reversible refractive index change upon absorption and release of CO(2) gas molecules, and does not require the presence of humidity to operate. By functionalizing a silicon microring resonator with a thin layer of the polymer, we could detect CO(2) gas concentrations in the 0-500ppm range with a sensitivity of 6 × 10(-9) RIU/ppm and a detection limit of 20ppm. The microring transducer provides a potential integrated solution in the development of low-cost and compact CO(2) sensors that can be deployed as part of a sensor network for accurate environmental monitoring of greenhouse gases.

  11. Wet scrubber technology for tritium confinement at ITER

    Energy Technology Data Exchange (ETDEWEB)

    Perevezentsev, A.N., E-mail: alexander.perevezentsev@iter.org [ITER Organization, CS 90 046, 13067 St Paul lez Durance Cedex (France); Andreev, B.M.; Rozenkevich, M.B.; Pak, Yu.S.; Ovcharov, A.V.; Marunich, S.A. [Mendeleev University of Chemical Technology, 125047 Miusskaya Sq. 9, Moscow (Russian Federation)

    2010-12-15

    Operation of the ITER machine with tritium plasma requires tritium confinement systems to protect workers and the environment. Tritium confinement at ITER is based on multistage approach. The final stage provides tritium confinement in building sectors and consists of building's walls as physical barriers and control of sub-atmospheric pressure in those volumes as a dynamic barrier. The dynamic part of the confinement function shall be provided by safety important components that are available all the time when required. Detritiation of air prior to its release to the environment is based on catalytic conversion of tritium containing gaseous species to water vapour followed by their isotopic exchange with liquid water in scrubber column of packed bed type. Wet scrubber technology has been selected because of its advantages over conventional air detritiation technique based on gas drying by water adsorption. The most important design target of system availability was very difficult to meet with conventional water adsorption driers. This paper presents results of experimental trial for validation of wet scrubber technology application in the ITER tritium confinement system and process evaluation using developed simulation computer code.

  12. Applications of stable isotope analysis to atmospheric trace gas budgets

    Directory of Open Access Journals (Sweden)

    Brenninkmeijer C. A.M.

    2009-02-01

    Full Text Available Stable isotope analysis has become established as a useful method for tracing the budgets of atmospheric trace gases and even atmospheric oxygen. Several new developments are briefly discussed in a systematic way to give a practical guide to the scope of recent work. Emphasis is on applications and not on instrumental developments. Processes and reactions are less considered than applications to resolve trace gas budgets. Several new developments are promising and applications hitherto not considered to be possible may allow new uses.

  13. Development of a tritium dispersion code

    International Nuclear Information System (INIS)

    Bell, R.P.; Davis, M.W.; Joseph, S.; Wong, K.Y.

    1985-01-01

    This paper describes the development and verification of a computer code designed to calculate the radiation dose to man following acute or chronic atmospheric releases of tritium gas and oxide from a point source. The Ontario Hydro Tritium Dispersion Code calculates tritium concentrations in air, soil, and vegetation and doses to man resulting from inhalation/immersion and ingestion of food, milk meat and water. The deposition of HT to soil, conversion of HT to HTO by soil enzymes and resuspension of HTO to air have been incorporated into the terrestrial compartment model and are unique features of the code. Sensitivity analysis has identified the HT deposition velocity and the equivalent water depth of the vegetation compartment as two parameters which have a strong influence on dose calculations. Tritium concentrations in vegetation and soil calculated by the code were in reasonable agreement with experimental results. The radiological significance of including the mechanisms of HT to HTO conversion and resuspension of HTO to air is illustrated

  14. Position sensitive proportional counter for measurement of tritium labelled gas movement

    International Nuclear Information System (INIS)

    Mori, Chizuo; Nakamoto, Makihiko; Uritani, Akira; Watanabe, Tamaki

    1984-01-01

    A position sensitive proportional counter of a charge division type with a single resistive anode wire was constructed for the measurement of the movement of 3 H labelled gas which is flowing or diffusing in a pipe. The introduction of resistors between the anode wire and pre-amplifiers brought a uniform detection efficiency for 3 H β-rays throughout the counter. The position resolution was 3.1 mm FWHM. Detection efficiency was almost 100% uniformly over about 700 mm in the total anode length of 740 mm. The movement of 3 H labelled gas could be measured effectively. (author)

  15. Tritium compatibility of alumina and Fosterite

    Energy Technology Data Exchange (ETDEWEB)

    Coffin, D.O.

    1979-09-01

    Many pressure measurements are required to control processing of the fuel gases associated with fusion power reactors. Since most pressure transducers respond to changes in pressure sensitive electrical parameters, insulators will be required to withstand chronic exposures to concentrated tritium. For this investigation samples of alumina and Fosterite were exposed to concentrated tritium gas for 11 weeks. Gas phase impurities were then analyzed for clues that would indicate decomposition of the exposed materials. The only gaseous impurity resulting from these tritium exposures was tritio-methane, which is always produced when tritium is stored in stainless steel containers. There was no evidence that either alumina or Fosterite decomposed in the presence of tritium.

  16. Tritium removal by hydrogen isotopic exchange between hydrogen gas and water on hydrophobic catalyst

    International Nuclear Information System (INIS)

    Morishita, T.; Isomura, S.; Izawa, H.; Nakane, R.

    1980-01-01

    Many kinds of the hydrophobic catalysts for hydrogen isotopic exchange between hydrogen gas and water have been prepared. The carriers are the hydrophobic organic materials such as polytetrafluoroethylene(PTFE), monofluorocarbon-PTFE mixture(PTFE-FC), and styrene-divinylbenzene copolymer(SDB). 0.1 to 2 wt % Pt is deposited on the carriers. The Pt/SDB catalyst has much higher activity than the Pt/PTFE catalyst and the Pt/PTFE-FC catalyst shows the intermediate value of catalytic activity. The observation of electron microscope shows that the degrees of dispersion of Pt particles on the hydrophobic carriers result in the difference of catalytic activities. A gas-liquid separated type column containing ten stages is constructed. Each stage is composed of both the hydrophobic catalyst bed for the hydrogen gas/water vapor isotopic exchange and the packed column type bed for the water vapor/liquid water isotopic exchange. In the column hydrogen gas and water flow countercurrently and hydrogen isotopes are separated

  17. Coalbed gas desorption in canisters: Consumption of trapped atmospheric oxygen and implications for measured gas quality

    International Nuclear Information System (INIS)

    Jin, Hui; Schimmelmann, Arndt; Mastalerz, Maria; Pope, James; Moore, Tim A.

    2010-01-01

    Desorption canisters are routinely employed to quantify coalbed gas contents in coals. If purging with inert gas or water flooding is not used, entrapment of air with ∝ 78.08 vol.% nitrogen (N 2 ) in canisters during the loading of coal results in contamination by air and subsequent overestimates of N 2 in desorbed coalbed gas. Pure coalbed gas does not contain any elemental oxygen (O 2 ), whereas air contamination originally includes ∝ 20.95 vol.% O 2 and has a N 2 /O 2 volume ratio of ∝ 3.73. A correction for atmospheric N 2 is often attempted by quantifying O 2 in headspace gas and then proportionally subtracting atmospheric N 2 . However, this study shows that O 2 is not a conservative proxy for air contamination in desorption canisters. Time-series of gas chromatographic (GC) compositional data from several desorption experiments using high volatile bituminous coals from the Illinois Basin and a New Zealand subbituminous coal document that atmospheric O 2 was rapidly consumed, especially during the first 24 h. After about 2 weeks of desorption, the concentration of O 2 declined to near or below GC detection limits. Irreversible loss of O 2 in desorption canisters is caused by biological, chemical, and physical mechanisms. The use of O 2 as a proxy for air contamination is justified only immediately after loading of desorption canisters, but such rapid measurements preclude meaningful assessment of coalbed gas concentrations. With increasing time and progressive loss of O 2 , the use of O 2 content as a proxy for atmospheric N 2 results in overestimates of N 2 in desorbed coalbed gas. The indicated errors for nitrogen often range in hundreds of %. Such large analytical errors have a profound influence on market choices for CBM gas. An erroneously calculated N 2 content in CBM would not meet specifications for most pipeline-quality gas. (author)

  18. Atmospheric Gas Tracers in Groundwater: Theory, Sampling. Measurement and Interpretation

    International Nuclear Information System (INIS)

    Bayari, C.S.

    2002-01-01

    Some of the atmospheric gasses posses features that are sought in an environmental tracer of hydrogeologic interest. Among these, chlorofluorocarbons, sulfur hegzafluoride, carbon tetrachloride, methyl chloroform, krypton-85 etc. have found increasing use in groundwater age dating studies during the last ten years. This paper explains the theory of their use as tracer and discusses the major concerns as related to their sampling and analyses. Factors affecting their applicability and the approach to interpret tracer gas data is briefly outlined

  19. Improvement of Cooling Technology through Atmosphere Gas Management

    Energy Technology Data Exchange (ETDEWEB)

    Renard, Michel; Dosogne, Edgaar; Crutzen, Jean Pierre; Raick, Jean Mare [DREVER INTERNATIONAL S.A., Liege (Belgium); Ji, Ma Jia; Jun, Lv; Zhi, Ma Bing [SHOUGANG Cold Rolling Mill Headquarter, Beijin (China)

    2009-12-15

    The production of advanced high strength steels requires the improvement of cooling technology. The use of high cooling rates allows relatively low levels of expensive alloying additions to ensure sufficient hardenability. In classical annealing and hot-dip galvanizing lines a mixing station is used to provide atmosphere gas containing 3-5% hydrogen and 97-95% nitrogen in the various sections of the furnace, including the rapid cooling section. Heat exchange enhancement in this cooling section can be insured by the increased hydrogen concentration. Driver international developed a patented improvement of cooling technology based on the following features: pure hydrogen gas is injected only in the rapid cooling section whereas the different sections of the furnace are supplied with pure nitrogen gas: the control of flows through atmosphere gas management allows to get high hydrogen concentration in cooling section and low hydrogen content in the other furnace zones. This cooling technology development insures higher cooling rates without additional expensive hydrogen gas consumption and without the use of complex sealing equipment between zones. In addition reduction in electrical energy consumption is obtained. This atmosphere control development can be combined with geometrical design improvements in order to get optimised cooling technology providing high cooling rates as well as reduced strip vibration amplitudes. Extensive validation of theoretical research has been conducted on industrial lines. New lines as well as existing lines, with limited modifications, can be equipped with this new development. Up to now this technology has successfully been implemented on 6 existing and 7 new lines in Europe and Asia.

  20. Modification and testing of the Sandia Laboratories Livermore tritium decontamination systems

    International Nuclear Information System (INIS)

    Gildea, P.D.; Birnbaum, H.G.; Wall, W.R.

    1978-08-01

    Sandia Laboratories, Livermore, has put into operation a new facility, the Tritium Research Laboratory. The laboratory incorporates containment and cleanup facilities such that any tritium accidentally released is captured rather than vented to the atmosphere. This containment is achieved with hermetically sealed glove boxes that are connected on demand by manifolds to two central decontamination systems called the Gas Purification System (GPS) and the Vacuum Effluent Recovery System (VERS). The primary function of the GPS is to remove tritium and tritiated water vapor from the glove box atmosphere. The primary function of the VERS is to decontaminate the gas exhausted from the glove box pressure control systems and vacuum pumps in the building before venting the gas to the stack. Both of these systems are designed to remove tritium to the few parts per billion range. Acceptance tests at the manufacturer's plant and preoperational testing at Livermore demonstrated that the systems met their design specifications. After preoperational testing the Gas Purification System was modified to enhance the safety of maintanance operations. Both the Gas Purification System and the Vacuum Effluent Recovery System were performance tested with tritium. Results show that concentraion reduction factors (ratio of inlet to exhaust concentrations) much in excess of 1000 per pass have been achieved for both systems at inlet concentrations of 1 ppM or less

  1. Modification and testing of the Sandia Laboratories Livermore tritium decontamination systems

    International Nuclear Information System (INIS)

    Gildea, P.D.; Birnbaum, H.G.; Wall, W.R.

    1979-01-01

    Sandia Laboratories, Livermore, has put into operation a new facility, the Tritium Research Laboratory. The laboratory incorporates containment and cleanup facilities such that any tritium accidentally released is captured rather than vented to the atmosphere. This containment is achieved with hermetically sealed glove boxes that are connected on demand by manifolds to two central decontamination systems called the Gas Purification System (GPS) and the Vacuum Effluent Recovery System (VERS). The primary function of the GPS is to remove tritium and tritiated water vapor from the glove box atmosphere. The primary function of the VERS is to decontaminate the gas exhausted from the glove box pressure control systems and vacuum pumps in the building before venting the gas to the stack. Both of these systems are designed to remove tritium to the few parts per billion range. Acceptance tests at the manufacturer's plant and preoperational testing at Livermore demonstrated that the systems met their design specifications. After preoperational testing the Gas Purification System was modified to enhance the safety of maintanance operations. Both the Gas Purification System and the Vacuum Effluent Recovery System were performance tested with tritium. Results show that concentration reduction factors (ratio of inlet to exhaust concentrations) much in excess of 1000 per pass have been achieved for both systems at inlet concentrations of 1 ppM or less

  2. Tritium accounting for PHWR plants

    International Nuclear Information System (INIS)

    Nair, P.S.; Duraisamy, S.

    2012-01-01

    Tritium, the radioactive isotope of hydrogen, is produced as a byproduct of the nuclear reactions in the nuclear power plants. In a Pressurized Heavy Water Reactor (PHWR) tritium activity is produced in the Heat Transport and Moderator systems due to neutron activation of deuterium in heavy water used in these systems. Tritium activity build up occurs in some of the water systems in the PHWR plants through pick up from the plant atmosphere, inadvertent D 2 O ingress from other systems or transfer during processes. The tritium, produced by the neutron induced reactions in different systems in the reactor undergoes multiple processes such as escape through leaks, storage, transfer to external locations, decay, evaporation and diffusion and discharge though waste streams. Change of location of tritium inventory takes place during intentional transfer of heavy water, both reactor grade and downgraded, from one system to another. Tritium accounting is the application of accounting techniques to maintain knowledge of the tritium inventory present in different systems of a facility and to construct activity balances to detect any discrepancy in the physical inventories. It involves identification of all the tritium hold ups, transfers and storages as well as measurement of tritium inventories in various compartments, decay corrections, environmental release estimations and evaluation of activity generation during the accounting period. This paper describes a methodology for creating tritium inventory balance based on periodic physical inventory taking, tritium build up, decay and release estimations. Tritium accounting in the PHWR plants can prove to be an effective regulatory tool to monitor its loss as well as unaccounted release to the environment. (author)

  3. Tritium in the environment. Knowledge synthesis

    International Nuclear Information System (INIS)

    2009-01-01

    This report first presents the nuclear and physical-chemical properties of tritium and addresses the notions of bioaccumulation, bio-magnification and remanence. It describes and comments the natural and anthropic origins of tritium (natural production, quantities released in the environment in France by nuclear tests, nuclear plants, nuclear fuel processing plants, research centres). It describes how tritium is measured as a free element (sampling, liquid scintillation, proportional counting, enrichment method) or linked to organic matter (combustion, oxidation, helium-3-based measurement). It discusses tritium concentrations noticed in different parts of the environment (soils, continental waters, sea). It describes how tritium is transferred to ecosystems (transfer of atmospheric tritium to ground ecosystems, and to soft water ecosystems). It discusses existing models which describe the behaviour of tritium in ecosystems. It finally describes and comments toxic effects of tritium on living ground and aquatic organisms

  4. Atmospheric aerosol and gas sensing using Scheimpflug lidar

    Science.gov (United States)

    Mei, Liang; Brydegaard, Mikkel

    2015-04-01

    This work presents a new lidar technique for atmospheric remote sensing based on Scheimpflug principle, which describes the relationship between nonparallel image- and object-planes[1]. When a laser beam is transmitted into the atmosphere, the implication is that the backscattering echo of the entire illuminated probe volume can be in focus simultaneously without diminishing the aperture. The range-resolved backscattering echo can be retrieved by using a tilted line scan or two-dimensional CCD/CMOS camera. Rather than employing nanosecond-pulsed lasers, cascade detectors, and MHz signal sampling, all of high cost and complexity, we have developed a robust and inexpensive atmospheric lidar system based on compact laser diodes and array detectors. We present initial applications of the Scheimpflug lidar for atmospheric aerosol monitoring in bright sunlight, with a 3 W, 808 nm CW laser diode. Kilohertz sampling rates are also achieved with applications for wind speed and entomology [2]. Further, a proof-of-principle demonstration of differential absorption lidar (DIAL) based on the Scheimpflug lidar technique is presented [3]. By utilizing a 30 mW narrow band CW laser diode emitting at around 760 nm, the detailed shape of an oxygen absorption line can be resolved remotely with an integration time of 6 s and measurement cycle of 1 minute during night time. The promising results demonstrated in this work show potential for the Scheimpflug lidar technique for remote atmospheric aerosol and gas sensing, and renews hope for robust and realistic instrumentation for atmospheric lidar sensing. [1] F. Blais, "Review of 20 years of range sensor development," Journal of Electronic Imaging, vol. 13, pp. 231-243, Jan 2004. [2] M. Brydegaard, A. Gebru, and S. Svanberg, "Super resolution laser radar with blinking atmospheric particles - application to interacting flying insects " Progress In Electromagnetics Research, vol. 147, pp. 141-151, 2014. [3] L. Mei and M. Brydegaard

  5. Tritium transport studies with use of the ISEP NPA during tritium trace experimental campaign on JET

    International Nuclear Information System (INIS)

    Mironov, M I; Afanasyev, V I; Murari, A; Santala, M; Beaumont, P

    2010-01-01

    The neutral particle analyzer (NPA) known as ISEP (Ion SEParator) was applied to measure the tritium neutral flux during the tritium trace experiment (TTE) on JET. The energy dependence (in the 5-28 keV energy range) of the tritium neutral flux rise time after a short ∼100 ms tritium gas puff into deuterium plasmas has been observed for the first time. The dependence has been interpreted as being due to the penetration of the tritium ions from the plasma boundary into the core and has been used for the calculation of the tritium diffusion coefficient and convective velocity values.

  6. Adsorption of radioactive I2 gas onto atmospheric aerosol

    International Nuclear Information System (INIS)

    Noguchi, Hiroshi; Murata, Mikio; Suzuki, Katsumi.

    1990-01-01

    Laboratory scale experiments on the adsorption of radioactive elemental iodine (I 2 ) gas onto atmospheric aerosol showed that the adsorption reached an equilibrium state in about twelve minutes at high initial I 2 concentrations. The proportion of iodine which was adsorbed on the aerosol gradually decreased with increading initial I 2 concentration ranging over 10 -13 to 10 -9 g/cm 3 at a reaction time of 31 min but was almost constant at a reaction time of 2 min. A fraction of iodine desorbed from particulate iodine as mainly I 2 gas. An adsorption isotherm of atmospheric aerosol for I 2 gas was estimated from the experimental data of long reaction time and high I 2 concentrations. Using this adsorption isotherm, a theoretical equation, which was similar to our previous equation, was derived to explain the experimental results. A geometric mean and standard deviation of sticking probability in the equation were estimated to be 1.2 x 10 -2 and 2.7, respectively. Almost all experimental data were within ranges of calculated results considering the geometric standard deviation of sticking probability. (author)

  7. Calculation of tritium release from reactor's stack

    International Nuclear Information System (INIS)

    Akhadi, M.

    1996-01-01

    Method for calculation of tritium release from nuclear to environment has been discussed. Part of gas effluent contain tritium in form of HTO vapor released from reactor's stack was sampled using silica-gel. The silica-gel was put in the water to withdraw HTO vapor absorbed by silica-gel. Tritium concentration in the water was measured by liquid scintillation counter of Aloka LSC-703. Tritium concentration in the gas effluent and total release of tritium from reactor's stack during certain interval time were calculated using simple mathematic formula. This method has examined for calculation of tritium release from JRR-3M's stack of JAERI, Japan. From the calculation it was obtained the value of tritium release as much as 4.63 x 10 11 Bq during one month. (author)

  8. A new tritium process monitor based on scintillating fibres

    International Nuclear Information System (INIS)

    Pacenti, P.; Edwards, R.A.H.; Monte, A. de; Campi, F.

    1998-01-01

    The main requirements for tritium monitoring in processes related with fusion fuel cycle are low tritium memory, fast response and accuracy, in decreasing order of importance. At present, in-line tritium monitoring in such tritium processing is done mostly using ionization chambers, which suffer a number of drawbacks: output and sensitivity depends on total gas pressure, composition and flow, etc., and have problems such as tritium memory and generally of saturation effect at high tritium concentrations. Solid scintillators can only work well with tritium if they offer a large surface area, because tritium is absorbed within the first microns of material. The present design uses entirely inorganic scintillator and construction materials, chosen to minimize tritium memory. The described on line and real time tritium detector presents some advantages in comparison with well established flow-through tritium process monitors, such as ionization chambers and thermal conductivity detectors. (authors)

  9. Tritium production and processing in a Tokamak reactor

    International Nuclear Information System (INIS)

    Leger, D.

    1986-09-01

    Important aspects of the tritium system in Tokamak reactors that have to be controlled are overviewed in this paper. The doubling time is one of them, that is to say the time required to produce, in addition to the tritium burned enough tritium to be able to supply the initial tritium inventory. Another one is the tritium permeation through walls. In addition to the permeation phenomena, large tritium inventories are trapped in the reactor structural material. Finally, the different atmospheres of halls, etc.., that can be contaminated with tritium, have to be reprocessed

  10. The movement of tritium in ecological systems

    International Nuclear Information System (INIS)

    Polevoy, Y; Laichter, Y.

    1988-11-01

    This literature survey summarizes the interaction of tritium gas and tritiated water with various components of the ecological system. The intake of tritium gas and tritiated water in plants and soil is described as well as the location of the highest measurable concentration. This information may serve as a basis for risk assessment from tritium to man through the food chain and enables effective tracing of its concentration in the environment. (author)

  11. Noble Gas Surface Flux Simulations And Atmospheric Transport

    Energy Technology Data Exchange (ETDEWEB)

    Carrigan, Charles R. [Lawrence Livermore National Lab. (LLNL), Livermore, CA (United States); Sun, Yunwei [Lawrence Livermore National Lab. (LLNL), Livermore, CA (United States); Simpson, Matthew D. [Lawrence Livermore National Lab. (LLNL), Livermore, CA (United States)

    2017-09-30

    Signatures from underground nuclear explosions or UNEs are strongly influenced by the containment regime surrounding them. The degree of gas leakage from the detonation cavity to the surface obviously affects the magnitude of surface fluxes of radioxenon that might be detected during the course of a Comprehensive Test Ban Treaty On-Site Inspection. In turn, the magnitude of surface fluxes will influence the downwind detectability of the radioxenon atmospheric signature from the event. Less obvious is the influence that leakage rates have on the evolution of radioxenon isotopes in the cavity or the downwind radioisotopic measurements that might be made. The objective of this letter report is to summarize our attempt to better understand how containment conditions affect both the detection and interpretation of radioxenon signatures obtained from sampling at the ground surface near an event as well as at greater distances in the atmosphere. In the discussion that follows, we make no attempt to consider other sources of radioactive noble gases such as natural backgrounds or atmospheric contamination and, for simplicity, only focus on detonation-produced radioxenon gases. Summarizing our simulations, they show that the decay of radioxenon isotopes (e.g., Xe-133, Xe-131m, Xe-133m and Xe-135) and their migration to the surface following a UNE means that the possibility of detecting these gases exists within a window of opportunity. In some cases, seeps or venting of detonation gases may allow significant quantities to reach the surface and be released into the atmosphere immediately following a UNE. In other release scenarios – the ones we consider here – hours to days may be required for gases to reach the surface at detectable levels. These release models are most likely more characteristic of “fully contained” events that lack prompt venting, but which still leak gas slowly across the surface for periods of months.

  12. Tritium Sequestration in Gen IV NGNP Gas Stream via Proton Conducting Ceramic Pumps

    International Nuclear Information System (INIS)

    Chen, Franglin Frank; Adams, Thad M.; Brinkman, Kyle; Reifsnider, Kenneth

    2011-01-01

    Several perovskite structured proton conductors based on SrCeO 3 and BaCeO 3 have been investigated in the project. The solid solutions for SrCeO 3 and BaCeO 3 were first investigated. The morphological and electrical properties of Ba 1-x Sr x Ce 0.8 Y 0.2 O 3-δ with x varying from 0 to 1 prepared by a modified Pechini method were investigated as potential high temperature proton conductors. Dense microstructures were achieved for all the samples upon sintering at 1500ees)C for 5 h. The phase structure analysis indicated that perovskite phase was formed for 0≤x≤0.2, while for x larger than 0.5, impurity phases of Sr 2 CeO 4 and Y 2 O 3 appeared. The stability tests indicated that the resistance to boiling water for Ba 1-x Sr x Ce 0.8 Y 0.2 O 3-δ was between that of BaCe 0.8 Y 0.2 O 3-δ and SrCe 0.8 Y 0.2 O 3-δ Due to the tendency of the reaction with CO 2 for both BaCe 0.8 Y 0.2 O 3-δ and SrCe 0.8 Y 0.2 O 3-δ , it was not surprising that Ba 1-x Sr x Ce 0.8 Y 0.2 O 3-δ was also not stable in CO 2 containing atmospheres. The conductivity tests indicated that Ba 1-x Sr x Ce 0.8 Y 0.2 O 3-δ possessed the electrical conductivity between BaCe 0.8 Y 0.2 O 3-δ and SrCe 0.8 Y 0.2 O 3-δ . The conductivity decreased and the activation energy increased with the increase in Sr content in Ba 1-x Sr x Ce 0.8 Y 0.2 O 3-δ .

  13. Tritium autoradiography

    International Nuclear Information System (INIS)

    Caskey, G.R. Jr.

    1981-01-01

    Hydrogen distribution and diffusion within many materials may be investigated by autoradiography if the radioactive isotope tritium is used in the study. Tritium is unstable and decays to helium-3 by emission of a low energy (18 keV) beta particle which may be detected photographically. The basic principles of tritium autoradiography will be discussed. Limitations are imposed on the technique by: (1) the low energy of the beta particles; (2) the solubility and diffusivity of hydrogen in materials; and (3) the response of the photographic emulsion to beta particles. These factors control the possible range of application of tritium autoradiography. The technique has been applied successfully to studies of hydrogen solubility and distribution in materials and to studies of hydrogen damage

  14. Tritium inventories and tritium safety design principles for the fuel cycle of ITER

    International Nuclear Information System (INIS)

    Cristescu, I.R.; Cristescu, I.; Doerr, L.; Glugla, M.; Murdoch, D.

    2007-01-01

    Within the tritium plant of ITER a total inventory of about 2-3 kg will be necessary to operate the machine in the DT phase. During plasma operation, tritium will be distributed in the different sub-systems of the fuel cycle. A tool for tritium inventory evaluation within each sub-system of the fuel cycle is important with respect to both the process of licensing ITER and also for operation. It is very likely that measurements of total tritium inventories may not be possible for all sub-systems; however, tritium accounting may be achieved by modelling its hold-up within each sub-system and by validating these models in real-time against the monitored flows and tritium streams between the sub-systems. To get reliable results, an accurate dynamic modelling of the tritium content in each sub-system is necessary. A dynamic model (TRIMO) for tritium inventory calculation reflecting the design of each fuel cycle sub-systems was developed. The amount of tritium needed for ITER operation has a direct impact on the tritium inventories within the fuel cycle sub-systems. As ITER will function in pulses, the main characteristics that influence the rapid tritium recovery from the fuel cycle as necessary for refuelling are discussed. The confinement of tritium within the respective sub-systems of the fuel cycle is one of the most important safety objectives. The design of the deuterium/tritium fuel cycle of ITER includes a multiple barrier concept for the confinement of tritium. The buildings are equipped with a vent detritiation system and re-circulation type room atmosphere detritiation systems, required for tritium confinement barrier during possible tritium spillage events. Complementarily to the atmosphere detritiation systems, in ITER a water detritiation system for tritium recovery from various sources will also be operated

  15. Experimental determination of the kinetic conversion rate of gaseous tritium into HTO

    International Nuclear Information System (INIS)

    Gulden, W.; Guenot, J.; Djerassi, H.; Clerc, H.

    1986-09-01

    To assess the impact of atmospheric tritium releases from a fusion plant to the environment, the dose to man usually is determined under the conservative assumption that all tritium is released in the more dangerous oxide form. To quantify this overprediction, experiments are presently being performed by CEA. Oxidation of tritium gas by soil and subsequent resuspension of HTO from soil to atmosphere is one of them. First results have been obtained by CEA on the kinetics of HTO resuspension from contaminated soils. Immediately after contamination, the fraction of the deposited activity which is resuspended to atmosphere is in the range of 1% to 5% per hour. This resuspension rate then decreases more or less slowly with time, depending on specific conditions

  16. Transfer of tritium into laying hen's meat and eggs at prolonged intake with atmospheric air, water and grass meal.

    Science.gov (United States)

    Baigazinov, Zh А; Lukashenko, S N; Karatayev, S S; Panitski, А V; Mamyrbayeva, А S; Baigazy, S А; Kozhakhanov, T Ye; Subbotina, L F

    2017-11-01

    Following a continuous intake of tritium (T) by laying hens' over a 55 day period, an increase of НТО concentration both in eggs and meat was observed over the first 2 weeks for intakes via inhalation and ingestion of water and grass meal. After this time, equilibrium of the T in these products occurred. It was found that when the intake of HTO is from water, air and grass meal, the ratio of its activity concentration in muscular tissue to that in eggs does not exceed 1, 4, and 6 respectively. The ratio of ОBТ concentration to that of НТО in the meat of hens (ОBТ/HTO) when intakes were from water, air and grass meal were 0.08, 0.09 and 0.7, respectively. Copyright © 2017 Elsevier Ltd. All rights reserved.

  17. Atmospheric Pressure Effect of Retained Gas in High Level Waste

    International Nuclear Information System (INIS)

    Weber, A.H.

    1999-01-01

    Isolated high level waste tanks in H-Area have unexplained changes in waste-level which have been attributed to environmental effects including pressure, temperature, and relative humidity. Previous studies at SRS have considered waste-level changes from causes not including the presence of gas in the salt cake. This study was undertaken to determine the effect of atmospheric pressure on gas in the salt cake and resultant changes in the supernate level of Tank 41H, and to model that effect if possible. A simple theory has been developed to account for changes in the supernate level in a high level waste tank containing damp salt cake as the response of trapped gases to changes in the ambient pressure. The gas is modeled as an ideal gas retained as bubbles within the interstitial spaces in the salt cake and distributed uniformly throughout the tank. The model does not account for consistent long term increases or decreases in the tank level. Any such trend in the tank level is attributed to changes in the liquid content in the tank (from condensation, evaporation, etc.) and is removed from the data prior to the void estimation. Short term fluctuations in the tank level are explained as the response of the entrained gas volume to changes in the ambient pressure. The model uses the response of the tank level to pressure changes to estimate an average void fraction for the time period of interest. This estimate of the void is then used to predict the expected level response. The theory was applied to three separate time periods of the level data for tank 41H as follows: (1) May 3, 1993 through August 3, 1993, (2) January 23, 1994 through April 21, 1994, and (3) June 4, 1994 through August 24, 1994. A strong correlation was found between fluctuations in the tank level and variations in the ambient pressure. This correlation is a clear marker of the presence of entrained gases in the tank. From model calculations, an average void fraction of 11 percent was estimated to

  18. Coalbed gas desorption in canisters: Consumption of trapped atmospheric oxygen and implications for measured gas quality

    Energy Technology Data Exchange (ETDEWEB)

    Jin, Hui; Schimmelmann, Arndt [Indiana University, Dept. of Geological Sciences, Bloomington, IN 47405-1405 (United States); Mastalerz, Maria [Indiana University, Indiana Geological Survey, Bloomington, IN 47405-2208 (United States); Pope, James [CRL Energy Ltd., 123 Blenheim Road, Christchurch (New Zealand); University of Canterbury, Dept. of Geological Sciences, Christchurch (New Zealand); Moore, Tim A. [University of Canterbury, Dept. of Geological Sciences, Christchurch (New Zealand); P.T. Arrow Energy Indonesia, Wisma Anugraha, Jl. Taman Kemang No. 32B, Jakarta Selatan (Indonesia)

    2010-01-07

    Desorption canisters are routinely employed to quantify coalbed gas contents in coals. If purging with inert gas or water flooding is not used, entrapment of air with {proportional_to} 78.08 vol.% nitrogen (N{sub 2}) in canisters during the loading of coal results in contamination by air and subsequent overestimates of N{sub 2} in desorbed coalbed gas. Pure coalbed gas does not contain any elemental oxygen (O{sub 2}), whereas air contamination originally includes {proportional_to} 20.95 vol.% O{sub 2} and has a N{sub 2}/O{sub 2} volume ratio of {proportional_to} 3.73. A correction for atmospheric N{sub 2} is often attempted by quantifying O{sub 2} in headspace gas and then proportionally subtracting atmospheric N{sub 2}. However, this study shows that O{sub 2} is not a conservative proxy for air contamination in desorption canisters. Time-series of gas chromatographic (GC) compositional data from several desorption experiments using high volatile bituminous coals from the Illinois Basin and a New Zealand subbituminous coal document that atmospheric O{sub 2} was rapidly consumed, especially during the first 24 h. After about 2 weeks of desorption, the concentration of O{sub 2} declined to near or below GC detection limits. Irreversible loss of O{sub 2} in desorption canisters is caused by biological, chemical, and physical mechanisms. The use of O{sub 2} as a proxy for air contamination is justified only immediately after loading of desorption canisters, but such rapid measurements preclude meaningful assessment of coalbed gas concentrations. With increasing time and progressive loss of O{sub 2}, the use of O{sub 2} content as a proxy for atmospheric N{sub 2} results in overestimates of N{sub 2} in desorbed coalbed gas. The indicated errors for nitrogen often range in hundreds of %. Such large analytical errors have a profound influence on market choices for CBM gas. An erroneously calculated N{sub 2} content in CBM would not meet specifications for most pipeline

  19. Tritium concentration monitor

    International Nuclear Information System (INIS)

    Shono, Kosuke.

    1991-01-01

    A device for measuring the concentration of tritium in gaseous wastes in a power plant and a nuclear fuel reprocessing plant is reduced in the size and improved in performance. The device of the present invention pressurizes a sampling gas and cools it to a dew point. Water content in the sampling gas cooled to the dew point is condensated and recovered to a fine tube-like water content recovering container. The concentration of the recovered condensates is measured by a tritium density analyzer. With such procedures, since the specimen is pressurized, the dew point can be elevated. Accordingly, the size of the cooling device can be decreased, enabling to contribute to the reduction of the size of the entire device. Further, since the water content recovering device is formed as a fine tube, the area of contact between the specimen gas and the liquid condensated water can be reduced. Accordingly, evaporation of the liquid condensates can be prevented. (I.S.)

  20. Analysis of trace levels of impurities and hydrogen isotopes in helium purge gas using gas chromatography for tritium extraction system of an Indian lead lithium ceramic breeder test blanket module.

    Science.gov (United States)

    Devi, V Gayathri; Sircar, Amit; Yadav, Deepak; Parmar, Jayraj

    2018-01-12

    In the fusion fuel cycle, the accurate analysis and understanding of the chemical composition of any gas mixture is of great importance for the efficient design of a tritium extraction and purification system or any tritium handling system. Methods like laser Raman spectroscopy and gas chromatography with thermal conductivity detector have been considered for hydrogen isotopes analyses in fuel cycles. Gas chromatography with a cryogenic separation column has been used for the analysis of hydrogen isotopes gas mixtures in general due to its high reliability and ease of operation. Hydrogen isotopes gas mixture analysis with cryogenic columns has been reported earlier using different column materials for percentage level composition. In the present work, trace levels of hydrogen isotopes (∼100 ppm of H 2 and D 2 ) have been analyzed with a Zeolite 5A and a modified γ-Al 2 O 3 column. Impurities in He gas (∼10 ppm of H 2 , O 2 , and N 2 ) have been analyzed using a Zeolite 13-X column. Gas chromatography with discharge ionization detection has been utilized for this purpose. The results of these experiments suggest that the columns developed were able to separate ppm levels of the desired components with a small response time (<6 min) and good resolution in both cases. © 2018 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

  1. Effects of interfering constituents on tritium smears

    International Nuclear Information System (INIS)

    Levi, G.D. Jr.; Cheeks, K.E.

    1993-01-01

    Tritium smears are performed by Health Protection Operations (HPO) to assess transferable contamination on work place surfaces, materials for movement outside Radiologically Controlled Areas (RCA), and product containers being shipped between facilities. Historically, gas proportional counters were used to detect transferable tritium contamination collected by smearing. Because tritium is a low-energy beta emitter, gas proportional counters do not provide the sensitivity or the counting efficiency to accurately measure the tritium activity on the smear. Liquid Scintillation Counters (LSC) provide greater counting efficiency for the low-energy beta particles along with greater reliability and reproducibility compared to gas flow proportional counters. The purpose of this technical evaluation was to determine the effects of interfering constituents such as filters, dirt and oil on the counting efficiency and tritium recoveries of tritium smears by LSC

  2. Tritium gettering from air with hydrogen uranyl phosphate

    International Nuclear Information System (INIS)

    Souers, P.C.; Uribe, F.S.; Stevens, C.G.; Tsugawa, T.T.

    1985-08-01

    The managers of all tritium facilities now worry about their emissions into the atmosphere. The only method for cleaning tritium out of air is to catalyze the formation of tritiated water which is adsorbed, along with the overwhelming bulk of naturally occurring water vapor, on a zeolite molecular sieve. This method generally costs several million dollars for a small system, because of the necessary steel ducting, compressors and holding tanks. We have long had the dream of finding another getter that might be cheaper to use and would, hopefully, not make tritiated water (HTO). In a previous paper, we discovered that hydrogen uranyl phosphate (HUP, with the formula HUO 2 PO 4 x 4H 2 O) getters 1 ppM of tritium gas out of moist air. This makes HUP the first known ''direct'' tritium getter to work in air. However, the tritium enters a hydroxyl network within the HUP, so that it is effectively still in ''water'' form within the HUP. Worse yet, we found up to 10% tritiated water formed during the previous gettering experiments. HUP is unusual in possessing the exceptionally low vapor pressure of 0.6 torr water vapor at 298 0 K. This allows HUP to be used in fairly dry environments. 14 refs., 3 figs., 2 tabs

  3. Tritium effluent removal system

    International Nuclear Information System (INIS)

    Lamberger, P.H.; Gibbs, G.E.

    1978-01-01

    An air detritiation system has been developed and is in routine use for removing tritium and tritiated compounds from glovebox effluent streams before they are released to the atmosphere. The system is also used, in combination with temporary enclosures, to contain and decontaminate airborne releases resulting from the opening of tritium containment systems during maintenance and repair operations. This detritiation system, which services all the tritium handling areas at Mound Facility, has played an important role in reducing effluents and maintaining them at 2 percent of the level of 8 y ago. The system has a capacity of 1.7 m 3 /min and has operated around the clock for several years. A refrigerated in-line filtration system removes water, mercury, or pump oil and other organics from gaseous waste streams. The filtered waste stream is then heated and passed through two different types of oxidizing beds; the resulting tritiated water is collected on molecular sieve dryer beds. Liquids obtained from regenerating the dryers and from the refrigerated filtration system are collected and transferred to a waste solidification and packaging station. Component redundancy and by-pass capabilities ensure uninterrupted system operation during maintenance. When processing capacity is exceeded, an evacuated storage tank of 45 m 3 is automatically opened to the inlet side of the system. The gaseous effluent from the system is monitored for tritium content and recycled or released directly to the stack. The average release is less than 1 Ci/day. The tritium effluent can be reduced by isotopically swamping the tritium; this is accomplished by adding hydrogen prior to the oxidizer beds, or by adding water to the stream between the two final dryer beds

  4. The LLNL portable tritium processing system

    International Nuclear Information System (INIS)

    Anon.

    1995-01-01

    The end of the Cold War significantly reduced the need for facilities to handle radioactive materials for the US nuclear weapons program. The LLNL Tritium Facility was among those slated for decommissioning. The plans for the facility have since been reversed, and it remains open. Nevertheless, in the early 1990s, the cleanup (the Tritium Inventory Removal Project) was undertaken. However, removing the inventory of tritium within the facility and cleaning up any pockets of high-level residual contamination required that we design a system adequate to the task and meeting today's stringent standards of worker and environmental protection. In collaboration with Sandia National Laboratory and EG ampersand G Mound Applied Technologies, we fabricated a three-module Portable Tritium Processing System (PTPS) that meets current glovebox standards, is operated from a portable console, and is movable from laboratory to laboratory for performing the basic tritium processing operations: pumping and gas transfer, gas analysis, and gas-phase tritium scrubbing. The Tritium Inventory Removal Project is now in its final year, and the portable system continues to be the workhorse. To meet a strong demand for tritium services, the LLNL Tritium Facility will be reconfigured to provide state-of-the-art tritium and radioactive decontamination research and development. The PTPS will play a key role in this new facility

  5. Laser Welding Test Results with Gas Atmospheres in Welding Chamber

    Energy Technology Data Exchange (ETDEWEB)

    Joung, Chang-Young; Hong, Jin-Tae; Ahn, Sung-Ho; Heo, Sung-Ho; Jang, Seo-Yun; Yang, Tae-Ho [Korea Atomic Energy Research Institute, Daejeon (Korea, Republic of)

    2015-10-15

    The weld beads of specimens welded under identical conditions in the helium and argon gas were cleaner, more regular, and steadier than those in a vacuum. The penetration depth of the FZ in the vacuum was much deeper than those in the helium and argon gas. To measure the irradiation properties of nuclear fuel in a test reactor, a nuclear fuel test rod instrumented with various sensors must be fabricated with assembly processes. A laser welding system to assemble the nuclear fuel test rod was designed and fabricated to develop various welding technologies of the fuel test rods to joint between a cladding tube and end-caps. It is an air-cooling optical fiber type and its emission modes are a continuous (CW) mode of which the laser generates continuous emission, and pulse (QCW) mode in which the laser internally generates sequences of pulses. We considered the system welding a sample in a chamber that can weld a specimen in a vacuum and inert gas atmosphere, and the chamber was installed on the working plate of the laser welding system. In the chamber, the laser welding process should be conducted to have no defects on the sealing area between a cladding tube and an end-cap.

  6. Atmospheric emissions from the upstream oil and gas industry

    International Nuclear Information System (INIS)

    Taylor, B.G.S.

    1994-01-01

    The results are presented of a study set up to determine the nature and levels of atmospheric emissions resulting from United Kingdom oil and gas exploration and production activities. The study was commissioned by the UK Offshore Operators Association. Emissions by the upstream oil and gas industry of common pollutants, such as carbon monoxide, sulphur dioxide and nitrous oxide, and ozone depletion chemicals were shown in each case to be less than 1% of total UK emissions. Greenhouse gas emissions in the industry arise mainly from production operations with a small but significant contribution from onshore activities. Carbon dioxide is the major component followed in descending order by nitrogen oxides, methane and volatile organic compounds. In 1991, these emissions formed 3.2%, 4.6%, 2.9% and 2.8% of the UK totals respectively; overall this represented only about 3% of UK global warming emissions. The evidence of this study illustrates that the industry, which produces 67% of the UK's primary energy, is successfully managing its operations in an environmentally responsible way. (3 figures, 3 tables) (UK)

  7. Modeling tritium transport in the environment

    International Nuclear Information System (INIS)

    Murphy, C.E. Jr.

    1986-01-01

    A model of tritium transport in the environment near an atmospheric source of tritium is presented in the general context of modeling material cycling in ecosystems. The model was developed to test hypotheses about the process involved in tritium cycling. The temporal and spatial scales of the model were picked to allow comparison to environmental monitoring data collected in the vicinity of the Savannah River Plant. Initial simulations with the model showed good agreement with monitoring data, including atmospheric and vegetation tritium concentrations. The model can also simulate values of tritium in vegetation organic matter if the key parameter distributing the source of organic hydrogen is varied to fit the data. However, because of the lack of independent conformation of the distribution parameter, there is still uncertainty about the role of organic movement of tritium in the food chain, and its effect on the dose to man

  8. Description of NORMTRI: a computer program for assessing the off-site consequences from air-borne releases of tritium during normal operation of nuclear facilities

    International Nuclear Information System (INIS)

    Raskob, W.

    1994-10-01

    The computer program NORMTRI has been developed to calculate the behaviour of tritium in the environment released into the atmosphere under normal operation of nuclear facilities. It is possible to investigate the two chemical forms tritium gas and tritiated water vapour. The conversion of tritium gas into tritiated water followed by its reemission back to the atmosphere as well as the conversion into organically bound tritium is considered. NORMTRI is based on the statistical Gaussian dispersion model ISOLA, which calculates the activity concentration in air near the ground contamination due to dry and wet deposition at specified locations in a polar grid system. ISOLA requires a four-parametric meteorological statistics derived from one or more years synoptic recordings of 1-hour-averages of wind speed, wind direction, stability class and precipitation intensity. Additional features of NORMTRI are the possibility to choose several dose calculation procedures, ranging from the equations of the German regulatory guidelines to a pure specific equilibrium approach. (orig.)

  9. In-pile test of tritium release from tritium breeding materials (VOM-21H experiment)

    International Nuclear Information System (INIS)

    Kurasawa, Toshimasa; Takeshita, Hidefumi; Watanabe, Hitoshi; Yoshida, Hiroshi.

    1986-10-01

    Material development and blanket design of lithium-based ceramics such as lithium oxide, lithium aluminate, lithium silicate and lithium zirconate have been performed in Japan, United State of America and Europian Communities. Lithium oxide is a most attractive candidate for tritium breeding materials because of its high lithium density, high thermal conductivity and good tritium release performance. This work has been done to clarify the characteristics of tritium release and recovery from Li 2 O by means of in-situ tritium release measurement. The effects of temperature and sweep gas composition on the tritium release were investigated in this VOM-21H Experiment. Good measurement of tritium release was achieved but there were uncertainties in reproduciblity of data. The experimental results show that the role of surface adsorption/desorption makes a significant contribution to the tritium release and tritium inventory. Also, it is necessary to define the rate limiting process either diffusion or surface adsorption/desorption. (author)

  10. Tritium pellet injection sequences for TFTR

    International Nuclear Information System (INIS)

    Houlberg, W.A.; Milora, S.L.; Attenberger, S.E.; Singer, C.E.; Schmidt, G.L.

    1983-01-01

    Tritium pellet injection into neutral deuterium, beam heated deuterium plasmas in the Tokamak Fusion Test Reactor (TFTR) is shown to be an attractive means of (1) minimizing tritium use per tritium discharge and over a sequence of tritium discharges; (2) greatly reducing the tritium load in the walls, limiters, getters, and cryopanels; (3) maintaining or improving instantaneous neutron production (Q); (4) reducing or eliminating deuterium-tritium (D-T) neutron production in non-optimized discharges; and (5) generally adding flexibility to the experimental sequences leading to optimal Q operation. Transport analyses of both compression and full-bore TFTR plasmas are used to support the above observations and to provide the basis for a proposed eight-pellet gas gun injector for the 1986 tritium experiments

  11. Tritium stripping by a catalytic exchange stripper

    International Nuclear Information System (INIS)

    Heung, L.K.; Gibson, G.W.; Ortman, M.S.

    1991-01-01

    A catalytic exchange process for stripping elemental tritium from gas streams has been demonstrated. The process uses a catalyzed isotopic exchange reaction between tritium in the gas phase and protium or deuterium in the solid phase on alumina. The reaction is catalyzed by platinum deposited on the alumina. The process has been tested with both tritium and deuterium. Decontamination factors (ration of inlet and outlet tritium concentrations) as high as 1000 have been achieved, depending on inlet concentration. The test results and some demonstrated applications are presented

  12. Separation of tritium from other hydrogen isotopes

    International Nuclear Information System (INIS)

    Roth, E.

    1988-01-01

    The paper describes a plant that has been operated at Marcoule for tritium production and used thermal diffusion enrichment, a facility that was built in Saclay to enrich hydrogen in tritium for low level measurements, and the Laue Langevin Institute tritium extraction plant. Details are given on the project under construction for the tritium separation facility at JET using Gas Chromatography, and on proposals for circuits for NET. Studies on catalysers for liquid phase catalytic exchange, on electrolysers, or different gas chromatography arrangements, are described. Systems designed for reprocessing plants, for detritiation of heavy water by distillation are briefly accounted for

  13. Tritium system design studies of fusion experimental breeder

    International Nuclear Information System (INIS)

    Deng Baiquan; Huang Jinhua

    2003-01-01

    A summary of the tritium system design studies for the engineering outline design of a fusion experimental breeder (FEB-E) is presented. This paper is divided into three sections. In first section, the geometry, loading features and tritium concentrations in liquid lithium of tritium breeding zones of blanket are described. The tritium flow chart corresponding to the tritium fuel cycle system has been constructed, and the inventories in ten subsystems are calculated using SWITRIM code in section 2. Results show that the necessary initial tritium storage to start up FEB-E with fusion power of 143 MW is about 319 g. In final section, the tritium leakage issues under different operation circumstances have been analyzed. It was found that the potential danger of tritium leakage could be resulted from the exhausted gas of the diverter system. It is important to elevate the tritium burnup fraction and reduce the tritium throughput. (authors)

  14. Effluent Treatment Facility tritium emissions monitoring

    International Nuclear Information System (INIS)

    Dunn, D.L.

    1991-01-01

    An Environmental Protection Agency (EPA) approved sampling and analysis protocol was developed and executed to verify atmospheric emissions compliance for the new Savannah River Site (SRS) F/H area Effluent Treatment Facility. Sampling equipment was fabricated, installed, and tested at stack monitoring points for filtrable particulate radionuclides, radioactive iodine, and tritium. The only detectable anthropogenic radionuclides released from Effluent Treatment Facility stacks during monitoring were iodine-129 and tritium oxide. This paper only examines the collection and analysis of tritium oxide

  15. Tritium monitoring at the Sandia Tritium Research Laboratory

    International Nuclear Information System (INIS)

    Devlin, T.K.

    1978-10-01

    Sandia Laboratories at Livermore, California, is presently beginning operation of a Tritium Research Laboratory (TRL). The laboratory incorporates containment and cleanup facilities such that any unscheduled tritium release is captured rather than vented to the atmosphere. A sophisticated tritium monitoring system is in use at the TRL to protect operating personnel and the environment, as well as ensure the safe and effective operation of the TRL decontamination systems. Each monitoring system has, in addition to a local display, a display in a centralized control room which, when coupled room which, when coupled with the TRL control computer, automatically provides an immediate assessment of the status of the entire facility. The computer controls a complex alarm array status of the entire facility. The computer controls a complex alarm array and integrates and records all operational and unscheduled tritium releases

  16. Measurement of HTO-HT in atmosphere using the Draeger (Drager) tube

    International Nuclear Information System (INIS)

    Huang, Z.; Harris, S.J.; Giorgio, P.R.

    1993-01-01

    It is clearly that, incorporation with the liquid scintillation counting, the Drager tube measuring system for Hydrogen allows the measurement of tritium contamination in atmosphere, e.g. HTO/HT (tritiated water vapour/tritium gas) simultaneously, at levels well below those derived air concentrations (DACs) prescribed by The International Commission on Radiological Protection (ICRP) and the UK Regulations. The novel tritium measuring system of Drager tube, in liquid phase or gel phase, can be used as a cheap, convenient and quick method of tritium detection

  17. Recuperated atmospheric SOFC/gas turbine hybrid cycle

    Science.gov (United States)

    Lundberg, Wayne

    2010-05-04

    A method of operating an atmospheric-pressure solid oxide fuel cell generator (6) in combination with a gas turbine comprising a compressor (1) and expander (2) where an inlet oxidant (20) is passed through the compressor (1) and exits as a first stream (60) and a second stream (62) the first stream passing through a flow control valve (56) to control flow and then through a heat exchanger (54) followed by mixing with the second stream (62) where the mixed streams are passed through a combustor (8) and expander (2) and the first heat exchanger for temperature control before entry into the solid oxide fuel cell generator (6), which generator (6) is also supplied with fuel (40).

  18. Recuperated atmosphere SOFC/gas turbine hybrid cycle

    Science.gov (United States)

    Lundberg, Wayne

    2010-08-24

    A method of operating an atmospheric-pressure solid oxide fuel cell generator (6) in combination with a gas turbine comprising a compressor (1) and expander (2) where an inlet oxidant (20) is passed through the compressor (1) and exits as a first stream (60) and a second stream (62) the first stream passing through a flow control valve (56) to control flow and then through a heat exchanger (54) followed by mixing with the second stream (62) where the mixed streams are passed through a combustor (8) and expander (2) and the first heat exchanger for temperature control before entry into the solid oxide fuel cell generator (6), which generator (6) is also supplied with fuel (40).

  19. HTO deposition through gas exchange between soil and atmosphere

    International Nuclear Information System (INIS)

    Feinhals, J.

    1988-06-01

    Theoretical considerations show that the ratio of HTO/H 2 O molecules, i.e. the specific activity, is not the same in atmospheric humidity and moisture absorption but differs by the so-called specific activity coefficient k. On this basis a computer model (ATHOS) was developed which allowed the calculation of both the surface contamination of the soil due to the gas exchange with a contaminated atmosphere and the depth-specific distribution of the soil acitvity. On the one hand the equations base on a modified Philip-de Vries theory, and on the other hand on a large number of soil column experiments which served the examination of the influence of parameters of microclimate and soil physics on the absorption and diffusion of tritiated water vapour under simulated conditions Above all the individual capability of each soil type to absorb moisture must be taken into consideration in connection with the HTO transfer. In this context theoretical and experimental examinations were carried out indicating a practice-related possibility to determine the soil-specific absorption capability. (orig./DG) [de

  20. Hazardous gas treatment using atmospheric pressure microwave discharges

    International Nuclear Information System (INIS)

    Mizeraczyk, Jerzy; Jasinski, Mariusz; Zakrzewski, Zenon

    2005-01-01

    Atmospheric pressure microwave discharge methods and devices used for producing non-thermal plasmas for control of gaseous pollutants are described in this paper. The main part of the paper is concerned with microwave torch discharges (MTDs). Results of laboratory experiments on plasma abatement of several volatile organic compounds (VOCs) in their mixtures with either synthetic air or nitrogen in low (∼100 W) and moderate (200-400 W) microwave torch plasmas at atmospheric pressure are presented. Three types of MTD generators, i.e. low-power coaxial-line-based MTDs, moderate-power waveguide-based coaxial-line MTDs and moderate-power waveguide-based MTDs were used. The gas flow rate and microwave (2.45 GHz) power delivered to the discharge were in the range of 1-3 litre min -1 and 100-400 W, respectively. The concentrations of the processed gaseous pollutants were from several to several tens of per cent. The results showed that the MTD plasmas fully decomposed the VOCs at a relatively low energy cost. The energy efficiency of decomposition of several gaseous pollutants reached 1000 g (kW-h) -1 . This suggests that MTD plasmas can be useful tools for decomposition of highly concentrated VOCs

  1. Tritium transport around nuclear facilities

    International Nuclear Information System (INIS)

    Murphy, C.E. Jr.; Sweet, C.W.

    1981-01-01

    The transport and cycling of tritium around nuclear facilities is reviewed with special emphasis on studies at the Savannah River Laboratory, Aiken, South Carolina. These studies have shown that the rate of deposition from the atmosphere, the site of deposition, and the subsequent cycling are strongly influenced by the compound with which the tritium is associated. Tritiated hydrogen is largely deposited in the soil, while tritiated water is deposited in the greatest quantity in the vegetation. Tritiated hydrogen is converted in the soil to tritiated water that leaves the soil slowly, through drainage and transpiration. Tritiated water deposited directly to the vegetation leaves the vegetation more rapidly after exposure. Only a small part of the tritium entering the vegetation becomes bound in organic molecules. However, it appears tht the existence of soil organic compounds with tritium concentrations greater than the equilibrium concentration in the associated water can be explained by direct metabolism of tritiated hydrogen in vegetation

  2. Tritium transport around nuclear faciliteis

    International Nuclear Information System (INIS)

    Murphy, C.E. Jr.; Sweet, C.W.

    1982-01-01

    The transport and cycling of tritium around nuclear facilities is reviewed with special emphasis on studies at the Savannah River Laboratory, Aiken, South Carolina. These studies have shown that the rate of deposition from the atmosphere, the site of deposition, and the subsequent cycling are strongly influenced by the compound with which the tritium is associated. Tritiated hydrogen is largely deposited in the soil, while tritiated water is deposited in the greatest quantity in the vegetation. Tritiated hydrogen is converted in the soil to tritiated water that leaves the soil slowly, through drainage and transpiration. Tritiated water deposited directly to the vegetation leaves the vegetation more rapidly after exposure. Only a small part of the tritium entering the vegetation becomes bound in organic molecules. However, it appears that the existence of soil organic compounds with tritium concentrations greater than the equilibrium concentration in the associated water can be explained by direct metabolism of tritiated hydrogen in vegetation. (J.P.N.)

  3. Experimental Investigation in Order to Determine Catalytic Package Performances in Case of Tritium Transfer from Water to Gas

    International Nuclear Information System (INIS)

    Bornea, Anisia; Peculea, M.; Zamfirache, M.; Varlam, Carmen

    2005-01-01

    The processes for hydrogen isotope's separation are very important for nuclear technology. One of the most important processes for tritium separation, is the catalyst isotope exchange water-hydrogen.Our catalytic package consists of Romanian patented catalysts with platinum on charcoal and polytetrafluoretylene (Pt/C/PTFE) and the ordered Romanian patented package B7 type. The catalytic package was tested in an isotope exchange facility for water detritiation at the Experimental Pilot Plant from ICIT Rm.Valcea.In a column of isotope exchange tritium is transferred from liquid phase (tritiated heavy water) in gaseous phase (hydrogen). In the experimental set-up, which was used, the column of catalytic isotope exchange is filled with successive layers of catalyst and ordered package. The catalyst consists of 95.5 wt.% of PTFE, 4.1 wt. % of carbon and 0.40 wt. % of platinum and was of Raschig rings 10 x 10 x 2 mm. The ordered package was B7 type consists of wire mesh phosphor bronze 4 x 1 wire and the mesh dimension is 0.18 x 0.48 mm.We analyzed the transfer phenomena of tritium from liquid to gaseous phase, in this system.The mass transfer coefficient which characterized the isotopic exchange on the package, were determined as function of experimental parameters

  4. Overview of light sources powered by tritium

    International Nuclear Information System (INIS)

    Wu Jian; Lei Jiarong; Liu Wenke

    2012-01-01

    Due to their long lifespan and stable intensity, light sources initiated by tritium instead of electricity or batteries are suitable for low level lighting applications. Therefore, tritium-based radioluminescent (RL) light sources are widely used in both military and civil applications. However, traditional tritium lights with the gas tube structure have several shortcomings: (1) the phosphors are opaque; (2) the glass tube is fragile and easily broken; and (3) the beta kinetic energy is attenuated due to the sorption by the gas; etc. As a result, further application of the tritium lights is limited. In this paper, the lighting mechanism and radiation safety of tritium-based RL light sources are briefly reviewed. Besides, the history and prospects of the development of tritium-based RL light source are discussed. Due to their long lifespan and stable intensity, light sources initiated by tritium instead of electricity or batteries are suitable for low level lighting applications. Therefore, tritium- based radioluminescent (RL) light sources are widely used in both military and civil applications. However, traditional tritium lights with the gas tube structure have several short- comings: (1) the phosphors are opaque; (2) the glass tube is fragile and easily broken; and (3) the beta kinetic energy is attenuated due to the sorption by the gas; etc. As a result, further application of the tritium lights is limited. In this paper, the lighting mechanism and radiation safety of tritium-based RL, light sources are briefly reviewed. Besides, the history and prospects of the development of tritium-based RL light source are discussed. (authors)

  5. Method of extracting tritium from heavy water

    International Nuclear Information System (INIS)

    Tsuchiya, Hiroyuki; Kikuchi, Makoto; Asakura, Yamato; Yusa, Hideo.

    1979-01-01

    Purpose: To extract tritium in heavy water by combining isotope exchange reaction with liquefaction distillation to increase the concentration of recovered tritium, thereby reducing the quantity of radioactive wastes recovered. Constitution: Heavy water containing tritium from a reactor is introduced into a tritium separator through a conduit pipe. On the other hand, a D 2 gas is introduced through the conduit pipe in the lower part of a tritium separator to transfer tritium into D 2 gas by isotope exchange. The D 2 gas containing DT is introduced into a liquefaction distillation tower together with an outlet gas of a converter supplied through a pipeline. The converter is filled with net-like metals of platinum group such as Pt, Ni, Pd and the like, and the D 2 gas affluent in DT, extracted from the distillation tower is converted into D 2 and T 2 . The gas which has been introduced into the liquefaction distillation tower is liquefied. The D 2 gas of low boiling point components reaches the tower top, and the T 2 gas of high boiling point components is concentrated at the tower bottom, and is rendered into tritium water in a recoupler and stored in a water storage apparatus. (Yoshino, Y.)

  6. First results of a simultaneous measurement of tritium and 14C in an ultra-low-background proportional counter for environmental sources of methane

    Energy Technology Data Exchange (ETDEWEB)

    Mace, Emily K.; Aalseth, Craig E.; Day, Anthony R.; Hoppe, Eric W.; Keillor, Martin E.; Moran, James J.; Panisko, Mark E.; Seifert, Allen; Tatishvili, Gocha; Williams, Richard M.

    2016-02-01

    Abstract Simultaneous measurement of tritium and 14C would provide an added tool for tracing organic compounds through environmental systems and is possible via beta energy spectroscopy of sample-derived methane in internal-source gas proportional counters. Since the mid-1960’s atmospheric tritium and 14C have fallen dramatically as the isotopic injections from above-ground nuclear testing have been diluted into the ocean and biosphere. In this work, the feasibility of simultaneous tritium and 14C measurements via proportional counters is revisited in light of significant changes in both the atmospheric and biosphere isotopics and the development of new ultra-low-background gas proportional counting capabilities for small samples (roughly 50 cc methane). A Geant4 Monte Carlo model of a Pacific Northwest National Laboratory (PNNL) proportional counter response to tritium and 14C is used to analyze small samples of two different methane sources to illustrate the range of applicability of contemporary simultaneous measurements and their limitations. Because the two methane sources examined were not sample size limited, we could compare the small-sample measurements performed at PNNL with analysis of larger samples performed at a commercial laboratory. The dual-isotope simultaneous measurement is well matched for methane samples that are atmospheric or have an elevated source of tritium (i.e. landfill gas). For samples with low/modern tritium isotopics (rainwater), commercial separation and counting is a better fit.

  7. Multiplex gas chromatography: an alternative concept for gas chromatographic analysis of planetary atmospheres

    Science.gov (United States)

    Valentin, J. R.

    1989-01-01

    Gas chromatography (GC) is a powerful technique for analyzing gaseous mixtures. Applied to the earth's atmosphere, GC can be used to determine the permanent gases--such as carbon dioxide, nitrogen, and oxygen--and to analyze organic pollutants in air. The U.S. National Aeronautics and Space Administration (NASA) has used GC in spacecraft missions to Mars (the Viking Biology Gas Exchange Experiment [GEX] and the Viking Gas Chromatograph-Mass Spectrometer [GC-MS]) and to Venus (the Pioneer Venus Gas Chromatograph [PVGC] on board the Pioneer Venus sounder probe) for determining the atmospheric constituents of these two planets. Even though conventional GC was very useful in the Viking and Pioneer missions, spacecraft constraints and limitations intrinsic to the technique prevented the collection of more samples. With the Venus probe, for instance, each measurement took a relatively long time to complete (10 min), and successive samples could not be introduced until the previous samples had left the column. Therefore, while the probe descended through the Venusian atmosphere, only three samples were acquired at widely separated altitudes. With the Viking mission, the sampling rate was not a serious problem because samples were acquired over a period of one year. However, the detection limit was a major disadvantage. The GC-MS could not detect simple hydrocarbons and simple alcohols below 0.1 ppm, and the GEX could not detect them below 1 ppm. For more complex molecules, the detection limits were at the parts-per-billion level for both instruments. Finally, in both the Viking and Pioneer missions, the relatively slow rate of data acquisition limited the number of analyses, and consequently, the amount of information returned. Similar constraints are expected in future NASA missions. For instance, gas chromatographic instrumentation is being developed to collect and analyze organic gases and aerosols in the atmosphere of Titan (one of Saturn's satellites). The Titan

  8. Universal tritium transmitter

    International Nuclear Information System (INIS)

    Cordaro, J. V.; Wood, M.

    2008-01-01

    At the Savannah River Site and throughout the National Nuclear Security Agency (NNSA) tritium is measured using Ion or Kanne Chambers. Tritium flowing through an Ion Chamber emits beta particles generating current flow proportional to tritium radioactivity. Currents in the 1 x 10 -15 A to 1 x 10 -6 A are measured. The distance between the Ion Chamber and the electrometer in NNSA facilities can be over 100 feet. Currents greater than a few micro-amperes can be measured with a simple modification. Typical operating voltages of 500 to 1000 Volts and piping designs require that the Ion Chamber be connected to earth ground. This grounding combined with long cable lengths and low currents requires a very specialized preamplifier circuit. In addition, the electrometer must be able to supply 'fail safe' alarm signals which are used to alert personnel of a tritium leak, trigger divert systems preventing tritium releases to the environment and monitor stack emissions as required by the United States federal Government and state governments. Ideally the electrometer would be 'self monitoring'. Self monitoring would reduce the need for constant checks by maintenance personnel. For example at some DOE facilities monthly calibration and alarm checks must be performed to ensure operation. NNSA presently uses commercially available electrometers designed specifically for this critical application. The problems with these commercial units include: ground loops, high background currents, inflexibility and susceptibility to Electromagnetic Interference (EMI) which includes RF and Magnetic fields. Existing commercial electrometers lack the flexibility to accommodate different Ion Chamber designs required by the gas pressure, type of gas and range. Ideally the electrometer could be programmed for any expected gas, range and high voltage output. Commercially available units do not have 'fail safe' self monitoring capability. Electronics used to measure extremely low current must have

  9. TFTR tritium inventory accountability system

    International Nuclear Information System (INIS)

    Saville, C.; Ascione, G.; Elwood, S.; Nagy, A.; Raftopoulos, S.; Rossmassler, R.; Stencel, J.; Voorhees, D.; Tilson, C.

    1995-01-01

    This paper discusses the program, PPPL (Princeton Plasma Physics Laboratory) Material Control and Accountability Plan, that has been implemented to track US Department of Energy's tritium and all other accountable source material. Specifically, this paper details the methods used to measure tritium in various systems at the Tokamak Fusion Test Reactor; resolve inventory differences; perform inventory by difference inside the Tokamak; process and measure plasma exhaust and other effluent gas streams; process, measure and ship scrap or waste tritium on molecular sieve beds; and detail organizational structure of the Material Control and Accountability group. In addition, this paper describes a Unix-based computerized software system developed at PPPL to account for all tritium movements throughout the facility. 5 refs., 2 figs

  10. Development of a tritium recovery system from CANDU tritium removal facility

    International Nuclear Information System (INIS)

    Draghia, M.; Pasca, G.; Porcariu, F.

    2015-01-01

    The main purpose of the Tritium Recovery System (TRS) is to reduce to a maximum possible extent the release of tritium from the facility following a tritium release in confinement boundaries and also to have provisions to recover both elemental and vapors tritium from the purging gases during maintenance and components replacement from various systems processing tritium. This work/paper proposes a configuration of Tritium Recovery System wherein elemental tritium and water vapors are recovered in a separated, parallel manner. The proposed TRS configuration is a combination of permeators, a platinum microreactor (MR) and a trickle bed reactor (TBR) and consists of two branches: one branch for elemental tritium recovery from tritiated deuterium gas and the second one for tritium recovery from streams containing a significant amount of water vapours but a low amount, below 5%, of tritiated gas. The two branches shall work in a complementary manner in such a way that the bleed stream from the permeators shall be further processed in the MR and TBR in view of achieving the required decontamination level. A preliminary evaluation of the proposed TRS in comparison with state of the art tritium recovery system from tritium processing facilities is also discussed. (authors)

  11. Development of a tritium recovery system from CANDU tritium removal facility

    Energy Technology Data Exchange (ETDEWEB)

    Draghia, M.; Pasca, G.; Porcariu, F. [SC.IS.TECH SRL, Timisoara (Romania)

    2015-03-15

    The main purpose of the Tritium Recovery System (TRS) is to reduce to a maximum possible extent the release of tritium from the facility following a tritium release in confinement boundaries and also to have provisions to recover both elemental and vapors tritium from the purging gases during maintenance and components replacement from various systems processing tritium. This work/paper proposes a configuration of Tritium Recovery System wherein elemental tritium and water vapors are recovered in a separated, parallel manner. The proposed TRS configuration is a combination of permeators, a platinum microreactor (MR) and a trickle bed reactor (TBR) and consists of two branches: one branch for elemental tritium recovery from tritiated deuterium gas and the second one for tritium recovery from streams containing a significant amount of water vapours but a low amount, below 5%, of tritiated gas. The two branches shall work in a complementary manner in such a way that the bleed stream from the permeators shall be further processed in the MR and TBR in view of achieving the required decontamination level. A preliminary evaluation of the proposed TRS in comparison with state of the art tritium recovery system from tritium processing facilities is also discussed. (authors)

  12. Tritium burning in inertial electrostatic confinement fusion facility

    Energy Technology Data Exchange (ETDEWEB)

    Ohnishi, Masami, E-mail: onishi@kansai-u.ac.jp [Department of Science and Engineering, Kansai University, 3-3-35 Yamate-cho, Suita, Osaka 564-8680 (Japan); Yamamoto, Yasushi; Osawa, Hodaka [Department of Science and Engineering, Kansai University, 3-3-35 Yamate-cho, Suita, Osaka 564-8680 (Japan); Hatano, Yuji; Torikai, Yuji [Hydrogen Isotope Science Center, University of Toyama, Gofuku, Toyama 930-8555 (Japan); Murata, Isao [Faculty of Engineering Environment and Energy Department, Osaka University, 2-1 Yamadaoka, Suita, Osaka 565-0871 (Japan); Kamakura, Keita; Onishi, Masaaki; Miyamoto, Keiji; Konda, Hiroki [Department of Science and Engineering, Kansai University, 3-3-35 Yamate-cho, Suita, Osaka 564-8680 (Japan); Masuda, Kai [Institute of Advanced Energy, Kyoto University, Gokasho, Uji, Kyoto 611-0011 (Japan); Hotta, Eiki [Interdisciplinary Graduate School of Science and Engineering, Tokyo Institute of Technology, 4259 Nagatsuda-cho, Midori-ku, Yokohama 226-8503 (Japan)

    2016-11-01

    Highlights: • An experiment on tritium burning is conducted in an inertial electrostatic confinement fusion (IECF) facility. • A deuterium–tritium gas mixture with 93% deuterium and 7% tritium is used. • The neutron production rate is measured to be 5–8 times more than that of pure deuterium gas. • The neutron production rate of the D–T gas mixture in 1:1 ratio is expected to be more than 10{sup 8}(1/sec) in the present D–T experiment. - Abstract: An experiment on tritium burning is conducted to investigate the enhancement in the neutron production rate in an inertial electrostatic confinement fusion (IECF) facility. The facility is designed such that it is shielded from the outside for safety against tritium and a getter pump is used for evacuating the vacuum chamber and feeding the fuel gas. A deuterium–tritium gas mixture with 93% deuterium and 7% tritium is used, and its neutron production rate is measured to be 5–8 times more than that of pure deuterium gas. Moreover, the results show good agreement with those of a simplified theoretical estimation of the neutron production rate. After tritium burning, the exhausted fuel gas undergoes a tritium recovery procedure through a water bubbler device. The amount of gaseous tritium released by the developed IECF facility after tritium burning is verified to be much less than the threshold set by regulations.

  13. Tritium burning in inertial electrostatic confinement fusion facility

    International Nuclear Information System (INIS)

    Ohnishi, Masami; Yamamoto, Yasushi; Osawa, Hodaka; Hatano, Yuji; Torikai, Yuji; Murata, Isao; Kamakura, Keita; Onishi, Masaaki; Miyamoto, Keiji; Konda, Hiroki; Masuda, Kai; Hotta, Eiki

    2016-01-01

    Highlights: • An experiment on tritium burning is conducted in an inertial electrostatic confinement fusion (IECF) facility. • A deuterium–tritium gas mixture with 93% deuterium and 7% tritium is used. • The neutron production rate is measured to be 5–8 times more than that of pure deuterium gas. • The neutron production rate of the D–T gas mixture in 1:1 ratio is expected to be more than 10"8(1/sec) in the present D–T experiment. - Abstract: An experiment on tritium burning is conducted to investigate the enhancement in the neutron production rate in an inertial electrostatic confinement fusion (IECF) facility. The facility is designed such that it is shielded from the outside for safety against tritium and a getter pump is used for evacuating the vacuum chamber and feeding the fuel gas. A deuterium–tritium gas mixture with 93% deuterium and 7% tritium is used, and its neutron production rate is measured to be 5–8 times more than that of pure deuterium gas. Moreover, the results show good agreement with those of a simplified theoretical estimation of the neutron production rate. After tritium burning, the exhausted fuel gas undergoes a tritium recovery procedure through a water bubbler device. The amount of gaseous tritium released by the developed IECF facility after tritium burning is verified to be much less than the threshold set by regulations.

  14. Doses due to tritium releases by NET - data base and relevant parameters on biological tritium behaviour

    International Nuclear Information System (INIS)

    Diabate, S.; Strack, S.

    1990-12-01

    This study gives an overview on the current knowledge about the behaviour of tritium in plants and in food chains in order to evaluate the ingestion pathway modelling of existing computer codes for dose estimations. The tritium uptake and retention by plants standing at the beginning of the food chains is described. The different chemical forms of tritium, which may be released into the atmosphere (HT, HTO and tritiated organics), and incorporation of tritium into organic material of plants are considered. Uptake and metabolism of tritiated compounds in animals and man are reviewed with particular respect to organically bound tritium and its significance for dose estimations. Some basic remarks on tritium toxicity are also included. Furthermore, a choice of computer codes for dose estimations due to chronic or accidental tritium releases has been compared with respect to the ingestion pathway. (orig.) [de

  15. Purification of tritium-free water

    International Nuclear Information System (INIS)

    Hussain, S.D.

    1982-10-01

    Ground water which has been out of contact with the atmosphere for a long time as compared to the half life of tritium (12.43 years) does not contain any measureable amount of tritium. Such water is called tritium-free water. It may contain dissolved and suspended impurities and has to be purified before it can be used for the preparation of blanks and standards required in the routine measurement of low level tritium in water samples. The purification of tritium-free water by distillation in a closed system has been described. The quality of processed tritium-free water was precisely checked at International Atomic Energy Agency (IAEA) Vienna and found satisfactory. (authors)

  16. Synthesis of tritium-labeled fosfomycin

    International Nuclear Information System (INIS)

    Mertel, H.E.; Meriwether, H.T.

    1982-01-01

    Tritium gas was used as a labeling agent for the preparation of [1,2- 3 H]fosfomycin. Introduction of tritium into a precursor, the synthesis including resolution of the intermediate racemic 1,2-epoxypropylphosphonic acid, and preparation of both amine and calcium salts of the labeled antibiotic are described. (author)

  17. Tritium Systems Test Facility. Volume II. Appendixes

    International Nuclear Information System (INIS)

    Anderson, G.W.; Battleson, K.W.; Bauer, W.

    1976-10-01

    This document includes the following appendices: (1) vacuum pumping, (2) tritium migration into the power cycle, (3) separation of hydrogen isotopes, (4) tritium research laboratory, (5) TSTF containment and cleanup, (6) instrumentation and control, (7) gas heating in torus, and (8) TSTF fuel loop operating procedures

  18. Process and system for removing tritium

    International Nuclear Information System (INIS)

    Ridgely, J.N.

    1976-01-01

    A process and system for removing tritium, particularly from high temperature gas cooled atomic reactors (HTGR), is disclosed. Portions of the reactor coolant, which is permeated with the pervasive tritium atom, are processed to remove the tritium. Under conditions of elevated temperature and pressure, the reactor coolant is combined with gaseous oxygen, resulting in the formation of tritiated water vapor from the tritium in the reactor coolant and the gaseous oxygen. The tritiated water vapor and the remaining gaseous oxygen are then successively removed by fractional liquefaction steps. The reactor coolant is then recirculated to the reactor

  19. Development of tritium handing technology(II)

    Energy Technology Data Exchange (ETDEWEB)

    Chung, H. S.; Ahn, D. H.; Kim, K. R. [KAERI, Taejon (Korea, Republic of); Yook, D. S.; Song, K. M.; Son, S. H. [KEPRI, Taejon (Korea, Republic of); Lee, K. J.; Jung, H. Y.; Song, M. C. [KAIST, Taejon (Korea, Republic of)

    2004-02-01

    The buildup rate of tritium in heavy water moderator and coolant of pressurized heavy water reactors in Wolsong Nuclear Power Plant is about 4MCi/a. The control of tritium is of increasing concern to the power reactor industry and general public in Korea. Metal tritides have the advantage of significantly decreasing the volume required to store tritium without increasing the pressure of storage vessel. Titanium hydride was safely used for the long-term storage of tritium. The experimental thermodynamic P-C-T data show that titanium soaks up hydrogen isotope gas at ambient temperature and modest pressures.

  20. Effects of tritium on electron multiplier performance

    International Nuclear Information System (INIS)

    Kerst, R.A.; Malinowski, M.E.

    1980-01-01

    In developing diagnostic instruments for fusion reactors, it is necessary to measure the effects of tritium contamination on channel electron multipliers (CEM). A CEM was exposed to T 2 pressures of up to 1.5 x 10 -1 Pa, with exposure quantities ranging up to 8800 Pa-s. The counting rate of the CEM is shown to consist of a prompt (Type I) signal caused by gas-phase tritium and a residual (Type II) signal, probably caused by near-surface tritium. The potential for using CEMs for observing the dynamics of tritium adsorption and absorption is discussed

  1. Contribution to the dosimetry of tritium in the presence of inactive or active gases

    International Nuclear Information System (INIS)

    Soudain, G.

    1966-01-01

    Tritium is a dangerous gas for man and the maximum admissible doses in the atmosphere are sufficiently low for the dosage to be fairly difficult. We have developed an apparatus for measuring selectively the contamination of air by this gas when it is alone or when it is associated with other gaseous contaminants. The differential apparatus using two ionization chambers makes it possible to eliminate a parasitic γ radiation field. In a few particular cases, the presence of the radio-active gas has been studied. From the practical point of view, the use of these chambers made of stainless steel makes for easier use since the problems connected with wall adsorption have been satisfactorily resolved. The method can be applied without restriction and very easily to the dosage of traces tritium in air or in the form of tritiated water or tritiated steam in the atmosphere. (author) [fr

  2. Electrolytic gettering of tritium from air

    International Nuclear Information System (INIS)

    Souers, P.C.; Tsugawa, R.T.; Stevens, C.G.

    1983-01-01

    We have removed 90% of 1 part-per-million tritium gas in air of 25% to 35% humidity by the dc electrical action of the solid proton electrolyte hydrogen uranyl phosphate (HUP). Gettering takes 5 to 24 hours for a 1 cm 2 HUP disc at 2 to 4 V in a static, 1200 cc gas volume. Hydrogen gas may be used to flush captured tritium through the HUP. Liquid water leaches out the tritium but water vapor is ineffective. This technique promises an alternative to the conventional catalyst/zeolite method

  3. Comparison of Tritium Component Failure Rate Data

    International Nuclear Information System (INIS)

    Lee C. Cadwallader

    2004-01-01

    Published failure rate values from the US Tritium Systems Test Assembly, the Japanese Tritium Process Laboratory, the German Tritium Laboratory Karlsruhe, and the Joint European Torus Active Gas Handling System have been compared. This comparison is on a limited set of components, but there is a good variety of data sets in the comparison. The data compared reasonably well. The most reasonable failure rate values are recommended for use on next generation tritium handling system components, such as those in the tritium plant systems for the International Thermonuclear Experimental Reactor and the tritium fuel systems of inertial fusion facilities, such as the US National Ignition Facility. These data and the comparison results are also shared with the International Energy Agency cooperative task on fusion component failure rate data

  4. Determination of low-level tritium concentrations in surface water and precipitation in the Czech Republic

    International Nuclear Information System (INIS)

    Maresova, Diana; Hanslik, Eduard; Sedlarova, Barbora; Juranova, Eva; Charles University, Prague

    2017-01-01

    Past tests of nuclear weapons in the atmosphere, nuclear energy facilities and tritium of natural origin are main sources of tritium in the environment. Thanks to its presence in environment and its favourable properties, tritium is used as a radiotracer. Since stopping of atmospheric nuclear tests, tritium in precipitation has been decreasing towards natural levels below 1 Bq l -1 and precise analyses of low level tritium activities are necessary. This paper focuses on tritium development at sites not influenced by any technogenic release of tritium in Elbe River basin (Bohemia) in the Czech Republic using liquid scintillation measurement with electrolytic enrichment. (author)

  5. Tritium detection in installations and in environment

    International Nuclear Information System (INIS)

    Calando, J.P.

    1986-04-01

    The different tritium detection devices in the atmosphere are reviewed: ionization chamber, proportional counters, Peltier effect, bubble-through device. Characteristics of those allowing to quantify the HTO form (more ''radiotoxic'' than T 2 form) are emphasized [fr

  6. Relating landfill gas emissions to atmospheric pressure using numerical modeling and state-space analysis

    DEFF Research Database (Denmark)

    Poulsen, T.G.; Christophersen, Mette; Moldrup, P.

    2003-01-01

    were applied: (I) State-space analysis was used to identify relations between gas flux and short-term (hourly) variations in atmospheric pressure. (II) A numerical gas transport model was fitted to the data and used to quantify short-term impacts of variations in atmospheric pressure, volumetric soil......-water content, soil gas permeability, soil gas diffusion coefficients, and biological CH4 degradation rate upon landfill gas concentration and fluxes in the soil. Fluxes and concentrations were found to be most sensitive to variations in volumetric soil water content, atmospheric pressure variations and gas...... permeability whereas variations in CH4 oxidation rate and molecular coefficients had less influence. Fluxes appeared to be most sensitive to atmospheric pressure at intermediate distances from the landfill edge. Also overall CH4 fluxes out of the soil over longer periods (years) were largest during periods...

  7. Computer program for assessing the human dose due to stationary release of tritium

    International Nuclear Information System (INIS)

    Saito, Masahiro; Raskob, Wolfgang

    2003-01-01

    The computer program TriStat (Tritium dose assessment for stationary release) has been developed to assess the dose to humans assuming a stationary release of tritium as HTO and/or HT from nuclear facilities. A Gaussian dispersion model describes the behavior of HT gas and HTO vapor in the atmosphere. Tritium concentrations in soil, vegetables and forage were estimated on the basis of specific tritium concentrations in the free water component and the organic component. The uptake of contamination via food by humans was modeled by assuming a forage compartment, a vegetable component, and an animal compartment. A standardized vegetable and a standardized animal with the relative content of major nutrients, i.e. proteins, lipids and carbohydrates, representing a standard Japanese diet, were included. A standardized forage was defined in a similar manner by using the forage composition for typical farm animals. These standard feed- and foodstuffs are useful to simplify the tritium dosimetry and the food chain related to the tritium transfer to the human body. (author)

  8. New arrangement for the air cleanup system to recover tritium

    International Nuclear Information System (INIS)

    Nishikawa, Masabumi; Takahashi, Kohsaku; Munakata, Kenzo; Fukada, Satoshi; Kotoh, Kenji; Takeishi, Toshiharu

    1997-01-01

    At present, the standard arrangement of the air cleanup system responsible for emergency tritium recovery from room air is a catalytic oxidation bed with a heater followed by an adsorption bed with a cooler. One disadvantage of this arrangement is that trouble with the heater or the cooler could result in a loss of capacity to recover tritium. Another disadvantage of the catalyst-adsorption-bed arrangement is that tritiated water must be recovered with a high decontamination factor after dilution with a large amount of water vapor in the working atmosphere. The performance of a new arrangement for the air cleanup system, which consists of a precious metal catalyst bed preceded by an adsorption bed without heating equipment, is discussed. According to calculations, most of the tritium released to the room air is recovered in the catalyst bed through oxidation, adsorption, and isotope exchange reaction when the new arrangement is applied. The adsorption bed placed before the catalyst bed dehumidifies the process gas to such a degree that the oxidation reaction of tritium in the catalyst bed is not hindered by water vapor. 15 refs., 6 figs., 6 tabs

  9. Technology and component development for a closed tritium cycle

    International Nuclear Information System (INIS)

    Hircq, B.; Penzhorn, R.D.; Haange, R.; Naruse, Y.

    1991-01-01

    A brief summary on recent advances in the field of tritium technology concerning the most important subsystems of the fuel cycle of a fusion reactor, i.e. the plasma exhaust pumping system, the exhaust gas clean up system, the isotope separation, the tritium storage and the tritium extraction from a blanket is provided. Experimental results, single component developments, and technical tests including those with relevants amounts of tritium that constitute the basis of proposed integral process concepts are described. 48 refs

  10. Characterization of contaminated oil with tritium, from of production of gas tripolar scintillators; Caracterizacao de oleo contaminado com tritio, proveniente da producao de centelhadores tripolares a gas

    Energy Technology Data Exchange (ETDEWEB)

    Potiens Junior, Ademar J.; Marumo, Julio T.; Goes, Marcos M.; Isiki, Vera L.K. [Instituto de Pesquisas Energeticas e Nucleares (IPEN), Sao Paulo, SP (Brazil)

    2001-07-01

    The objective of this work was to develop a methodology to estimate the activity level present in radioactive oil samples. This oil is derived from vacuum pumps used to produce tension protector of electronic equipment in telecommunication area. The method consisted in obtain a calibration curve in counts per minute versus tritium activity. After the equipment calibration it was analyzed 3 batches of radioactive oil samples. (author)

  11. Applications developed for byproduct 85Kr and tritium

    International Nuclear Information System (INIS)

    Remini, W.C.; Case, F.N.; Haff, K.W.; Tiegs, S.M.

    1983-01-01

    The radionuclides, krypton-85 and tritium, both of which are gases under ordinary conditions, are used in many applications in industries and by the military forces. Krypton-85 is produced during the fissioning of uranium and is released during the dissolution of spent-fuel elements. It is a chemically inert gas that emits 0.695-MeV beta rays and a small yield of 0.54-MeV gammas over a half life of 10.3 years. Much of the 85 Kr currently produced is released to the atmosphere; however, large-scale reprocessing of fuel will require collection of the gas and storage as a waste product. An alternative to storage is utilization, and since the chemical and radiation characteristics of 85 Kr make this radionuclide a relatively low hazard from the standpoint of contamination and biological significance, a number of uses have been developed. Tritium is produced as a byproduct of the nuclear-weapons program, and it has a half life of 12.33 years. It has a 0.01861-MeV beta emission and no gamma emission. The absence of a gamma-ray energy eliminates the need for external shielding of the devices utilizing tritium, thus making them easily transportable. Many of the applications require only small quantities of 85 Kr or tritium; however, these uses are important to the technology base of the nation. A significant development that has the potential for beneficial utilization of large quantities of 85 Kr and of tritium involves their use in the production of low-level lighting devices. Since these lights are free from external fuel supplies, have a long half life (> 10 years), are maintenance-free, reliable, and easily deployed, both military and civilian airfield-lighting applications are being studied

  12. Tritium pellet injector for TFTR

    International Nuclear Information System (INIS)

    Gouge, M.J.; Baylor, L.R.; Cole, M.J.; Combs, S.K.; Dyer, G.R.; Fehling, D.T.; Fisher, P.W.; Foust, C.R.; Langley, R.A.; Milora, S.L.; Qualls, A.L.; Wilgen, J.B.; Schmidt, G.L.; Barnes, G.W.; Persing, R.G.

    1992-01-01

    The tritium pellet injector (TPI) for the Tokamak Fusion Test Reactor (TFTR) will provide a tritium pellet fueling capability with pellet speeds in the 1- to 3-km/s range for the TFTR deuterium-tritium (D-T) phase. The existing TFTR deuterium pellet injector (DPI) has been modified at Oak Ridge National Laboratory (ORNL) to provide a four-shot, tritium-compatible, pipe-gun configuration with three upgraded single-stage pneumatic guns and a two-stage light gas gun driver. The TPI was designed to provide pellets ranging from 3.3 to 4.5 mm in diameter in arbitrarily programmable firing sequences at speeds up to approximately 1.5 km/s for the three single-stage drivers and 2.5 to 3 km/s for the two-stage driver. Injector operation is controlled by a programmable logic controller. The new pipe-gun injector assembly was installed in the modified DPI guard vacuum box, and modifications were made to the internals of the DPI vacuum injection line, including a new pellet diagnostics package. Assembly of these modified parts with existing DPI components was then completed, and the TPI was tested at ORNL with deuterium pellet. Results of the limited testing program at ORNL are described. The TPI is being installed on TFTR to support the D-D run period in 1992. In 1993, the tritium pellet injector will be retrofitted with a D-T fuel manifold and secondary tritium containment systems and integrated into TFTR tritium processing systems to provide full tritium pellet capability

  13. Studies on steps affecting tritium residence time in solid blanket

    International Nuclear Information System (INIS)

    Tanaka, Satoru

    1987-01-01

    For the self sustaining of CTR fuel cycle, the effective tritium recovery from blankets is essential. This means that not only tritium breeding ratio must be larger than 1.0, but also high recovering speed is required for the short residence time of tritium in blankets. Short residence time means that the tritium inventory in blankets is small. In this paper, the tritium residence time and tritium inventory in a solid blanket are modeled by considering the steps constituting tritium release. Some of these tritium migration processes were experimentally evaluated. The tritium migration steps in a solid blanket using sintered breeding materials consist of diffusion in grains, desorption at grain edges, diffusion and permeation through grain boundaries, desorption at particle edges, diffusion and percolation through interconnected pores to purging stream, and convective mass transfer to stream. Corresponding to these steps, diffusive, soluble, adsorbed and trapped tritium inventories and the tritium in gas phase are conceivable. The code named TTT was made for calculating these tritium inventories and the residence time of tritium. An example of the results of calculation is shown. The blanket is REPUTER-1, which is the conceptual design of a commercial reversed field pinch fusion reactor studied at the University of Tokyo. The experimental studies on the migration steps of tritium are reported. (Kako, I.)

  14. Risks of tritium and their mitigation

    International Nuclear Information System (INIS)

    Ichimasa, Y.; Shiba, H.; Ichimasa, M.; Chikuuti, M.; Akita, Y.

    1992-01-01

    In this study, the effects of an antibacterial drug, norfloxacin, and an antibiotic, clindamycin, on in vivo oxidation of tritium gas in rats were investigated. Wistar strain male rats were used. They were provided with a standard diet, water ad libitum, and maintained in glass metabolic cages of approximately 20 liters capacity. The air flow and temperature were controlled. To investigate the availability of norfloxacin and clindamycin on the inhibition effects of the oxidation of tritium gas, two types of the experiments were conducted one was that, before the exposure to tritium gas for 2 hours, norfloxacin or clindamycin was administrated to rats three times a day for 4 days, and the other was administration of a drug after tritium gas exposure. After the exposure to tritium gas, blood, the liver, urine and feces samples were collected from rats and the radioactivity of them was determined after combustion using a sample oxidizer. In the case of norfloxacin, tritium concentration in rat body decreased one fifth of that in non-treated rats. On the other hand, administration of clindamycin shortened the biological half-life of tritium in urine to three fifth of that of non-treated rats. (author)

  15. A Controlled Environment System For Measuring Plant-Atmosphere Gas Exchange

    Science.gov (United States)

    James M. Brown

    1975-01-01

    Describes an inexpensive, efficient system for measuring plant-atmosphere gas exchange. Designed to measure transpiration from potted tree seedlings, it is readily adaptable for measuring other gas exchanges or gas exchange by plant parts. Light level, air and root temperature can be precisely controlled at minimum cost.

  16. Methane generated from graphite--tritium interaction

    International Nuclear Information System (INIS)

    Coffin, D.O.; Walthers, C.R.

    1979-01-01

    When hydrogen isotopes are separated by cryogenic distillation, as little as 1 ppM of methane will eventually plug the still as frost accumulates on the column packings. Elemental carbon exposed to tritium generates methane spontaneously, and yet some dry transfer pumps, otherwise compatible with tritium, convey the gas with graphite rotors. This study was to determine the methane production rate for graphite in tritium. A pump manufacturer supplied graphite samples that we exposed to tritium gas at 0.8 atm. After 137 days we measured a methane synthesis rate of 6 ng/h per cm 2 of graphite exposed. At this rate methane might grow to a concentration of 0.01 ppM when pure tritium is transferred once through a typical graphite--rotor transfer pump. Such a low methane level will not cause column blockage, even if the cryogenic still is operated continuously for many years

  17. ACUTRI: a computer code for assessing doses to the general public due to acute tritium releases

    Energy Technology Data Exchange (ETDEWEB)

    Yokoyama, Sumi; Noguchi, Hiroshi [Japan Atomic Energy Research Inst., Tokai, Ibaraki (Japan). Tokai Research Establishment; Ryufuku, Susumu; Sasaki, Toshihisa; Kurosawa, Naohiro [Visible Information Center, Inc., Tokai, Ibaraki (Japan)

    2002-11-01

    Tritium, which is used as a fuel of a D-T burning fusion reactor, is the most important radionuclide for the safety assessment of a nuclear fusion experimental reactor such as ITER. Thus, a computer code, ACUTRI, which calculates the radiological impact of tritium released accidentally to the atmosphere, has been developed, aiming to be of use in a discussion of licensing of a fusion experimental reactor and an environmental safety evaluation method in Japan. ACUTRI calculates an individual tritium dose based on transfer models specific to tritium in the environment and ICRP dose models. In this calculation it is also possible to analyze statistically on meteorology in the same way as a conventional dose assessment method according to the meteorological guide of the Nuclear Safety Commission of Japan. A Gaussian plume model is used for calculating the atmospheric dispersion of tritium gas (HT) and/or tritiated water (HTO). The environmental pathway model in ACUTRI considers the following internal exposures: inhalation from a primary plume (HT and/or HTO) released from the facilities and inhalation from a secondary plume (HTO) reemitted from the ground following deposition of HT and HTO. This report describes an outline of the ACUTRI code, a user guide and the results of test calculation. (author)

  18. Tritium means of detection and of protection; Le tritium moyens de detection et de protection

    Energy Technology Data Exchange (ETDEWEB)

    Sutra-Fourcade, Y [Commissariat a l' Energie Atomique, Marcoule (France). Centre d' Etudes Nucleaires

    1967-07-01

    The report is an attempt to correlate present data concerning tritium, especially from the health physics points of view. The various detection and measurement methods are reviewed in turn: measurement of tritium in the atmosphere, in liquids and on surfaces. The operation of various types of apparatus is analyzed and the sensitivity limits deduced from laboratory tests are given. Otter sections are devoted to the means of protection which can be used against inhalation of tritium (ventilation, protective clothing) and to calculations of the changes in atmospheric pollution in a given place and of the time spent in a contaminated zone. The last part deals with the decontamination of equipment contaminated with tritium. (author) [French] Le rapport represente un essai de synthese des connaissances actuelles sur le tritium, essentiellement du point de vue de la radioprotection. Les differents moyens de detection et de mesure sont successivement passes en revue: mesure du tritium dans l'atmosphere, dans les liquides, sur les surfaces. Le fonctionnement de differents types d'appareils est analyse et les limites de sensibilite sont donnees d'apres les essais effectues en laboratoire. D'autres paragraphes sont consacres aux moyens de protection contre l'inhalation du tritium (ventilation, vetements de protection), a des calculs d'evolution de pollution atmospherique dans les locaux et de temps de presence en atmosphere contaminee. La derniere partie se rapporte a la de contamination de materiel contamine par du tritium. (auteur)

  19. Magmatic tritium

    International Nuclear Information System (INIS)

    Goff, F.; Aams, A.I.; McMurtry, G.M.; Shevenell, L.; Pettit, D.R.; Stimac, J.A.; Werner, C.

    1997-01-01

    This is the final report of a three-year, Laboratory-Directed Research and Development (LDRD) project at the Los Alamos National Laboratory. Detailed geochemical sampling of high-temperature fumaroles, background water, and fresh magmatic products from 14 active volcanoes reveal that they do not produce measurable amounts of tritium ( 3 H) of deep origin ( 2 O). On the other hand, all volcanoes produce mixtures of meteoric and magmatic fluids that contain measurable 3 H from the meteoric end-member. The results show that cold fusion is probably not a significant deep earth process but the samples and data have wide application to a host of other volcanological topics

  20. Behaviour of tritium in the environment

    International Nuclear Information System (INIS)

    1979-01-01

    Full text: There is considerable interest in the behaviour of radionuclides of global character that may be released to the environment through the development of nuclear power. Tritium is of particular interest due to its direct incorporation into water and organic tissue. Although there has been a large decrease (more than ten times) in tritium concentration since the stopping of nuclear weapons tests in the atmosphere, the construction in the near future of many water reactors and in the far future of fusion reactors could increase the present levels. Progress has been made during recent years in the assessment of tritium distribution, in detection methods and in biological studies While several meetings have given scientists an opportunity to present papers on tritium, no specific symposium on this topic has been organized by the IAEA since 1961. Thus the purpose of the meeting was to review recent advances and to report on the practical aspects of tritium utilization and monitoring. The symposium was jointly organized with OECD/NEA, in co-operation with the US Department of Energy and the Lawrence Livermore Laboratory. Papers were presented on distribution of tritium, evaluation of future discharges, measurement of tritium, tritium in the aquatic environment, tritium in the terrestrial environment, tritium in man and monitoring of tritium Very interesting papers were given on distribution of tritium and participants got a good idea of the circulation of this radionuclide Some new data were provided on tritium pollution from luminous compounds and we learnt that the tritium release of the Swiss luminous compounds industry is of the same order of magnitude as the tritium release of Windscale. Projections indicate that, in the USA, the total quantity of tritium contained in discarded digital watches will be equal, approximately ten years in the future, to the release of nuclear power reactors Whereas nuclear reactor discharges are controlled there is no control

  1. Controlling hydrophilicity of polymer film by altering gas flow rate in atmospheric-pressure homogeneous plasma

    International Nuclear Information System (INIS)

    Kang, Woo Seok; Hur, Min; Lee, Jae-Ok; Song, Young-Hoon

    2014-01-01

    Graphical abstract: - Highlights: • Controlling hydrophilicity of polymer film by varying gas flow rate is proposed in atmospheric-pressure homogeneous plasma treatment. • Without employing additional reactive gas, requiring more plasma power and longer treatment time, hydrophilicity of polyimide films was improved after the low-gas-flow plasma treatment. • The gas flow rate affects the hydrophilic properties of polymer surface by changing the discharge atmosphere in the particular geometry of the reactor developed. • Low-gas-flow induced wettability control suggests effective and economical plasma treatment. - Abstract: This paper reports on controlling the hydrophilicity of polyimide films using atmospheric-pressure homogeneous plasmas by changing only the gas flow rate. The gas flow changed the discharge atmosphere by mixing the feed gas with ambient air because of the particular geometry of the reactor developed for the study, and a low gas flow rate was found to be favorable because it generated abundant nitrogen or oxygen species that served as sources of hydrophilic functional groups over the polymer surface. After low-gas-flow plasma treatment, the polymer surface exhibited hydrophilic characteristics with increased surface roughness and enhanced chemical properties owing to the surface addition of functional groups. Without adding any reactive gases or requiring high plasma power and longer treatment time, the developed reactor with low-gas-flow operation offered effective and economical wettability control of polyimide films

  2. Release enhancement of tritium from graphite by addition of hydrogen

    International Nuclear Information System (INIS)

    Saeki, Masakatsu; Masaki, N.M.

    1989-01-01

    The release behavior of tritium from graphite was studied in pure He and He + H 2 atmosphere. The release from powdered graphite was significantly enhanced in hydrogen environment. Apparent diffusion coefficients of tritium in graphite also became much higher in an atmosphere containing hydrogen than values obtained in pure helium atmosphere. A careful investigation of the release processes resulted in the conclusion that the most important process of tritium behaviour in graphite was diffusion, but the desorption process of tritium from the surface played a significant role. The enhancement of the desorption process was controlled by atomic hydrogen. (orig.)

  3. Tritium migration studies at the Nevada Test Site

    International Nuclear Information System (INIS)

    Schulz, R.K.; Weaver, M.O.

    1993-05-01

    Emanation of tritium from waste containers is a commonly known phenomenon. Release of tritium from buried waste packages was anticipated; therefore, a research program was developed to study both the rate of tritium release from buried containers and subsequent migration of tritium through soil. Migration of tritium away from low-level radioactive wastes buried in Area 5 of the Nevada Test Site was studied. Four distinct disposal events were investigated. The oldest burial event studied was a 1976 emplacement of 3.5 million curies of tritium in a shallow land burial trench. In another event, 248 thousand curies of tritium was disposed of in an overpack emplaced 6 m below the floor of a low-level waste disposal pit. Measurement of the emanation rate of tritium out of 55 gallon drums to the overpack was studied, and an annual doubling of the emanation rate over a seven year period, ending in 1990, was found. In a third study, upward tritium migration in the soil, resulting in releases in the atmosphere were observed in a greater confinement disposal test. Releases of tritium to the atmosphere were found to be insignificant. The fourth event consisted of burial of 2.2 million curies of tritium in a greater confinement disposal operation. Emanation of tritium from the buried containers has been increasing since disposal, but no significant migration was found four years following backfilling of the disposal hole

  4. Tritium monitoring at NPP and enviromental area under survey

    International Nuclear Information System (INIS)

    Nurislamov, I.R.; Kham'yanov, L.P.; Panichkin, V.F.

    1983-01-01

    Methods and devices for tritium monitoring at NPP with the WWER-type reactors and the environment are described. Aqueous solutions of inorganic and organic compounds, water vapours in the air of NPP rooms and the environment atmosphere, free and bound water in soils and vegetation were the objects for monitoring. Methods of tritium sampling from the atmosphere as well as determination of its content in samples are presented. Special attention is paid to sample enrichment with tritium

  5. Tritium proof-of-principle pellet injector

    International Nuclear Information System (INIS)

    Fisher, P.W.

    1991-07-01

    The tritium proof-of-principle (TPOP) experiment was designed and built by Oak Ridge National Laboratory (ORNL) to demonstrate the formation and acceleration of the world's first tritium pellets for fueling of future fusion reactors. The experiment was first used to produce hydrogen and deuterium pellets at ORNL. It was then moved to the Tritium Systems Test Assembly at Los Alamos National Laboratory for the production of tritium pellets. The injector used in situ condensation to produce cylindrical pellets in a 1-m-long, 4-mm-ID barrel. A cryogenic 3 He separator, which was an integral part of the gun assembly, was capable of lowering 3 He levels in the feed gas to <0.005%. The experiment was housed to a glovebox for tritium containment. Nearly 1500 pellets were produced during the course of the experiment, and about a third of these were pure tritium or mixtures of deuterium and tritium. Over 100 kCi of tritium was processed through the experiment without incident. Tritium pellet velocities of 1400 m/s were achieved with high-pressure hydrogen propellant. The design, operation, and results of this experiment are summarized. 34 refs., 44 figs., 3 tabs

  6. Relation between plasma plume density and gas flow velocity in atmospheric pressure plasma

    International Nuclear Information System (INIS)

    Yambe, Kiyoyuki; Taka, Shogo; Ogura, Kazuo

    2014-01-01

    We have studied atmospheric pressure plasma generated using a quartz tube, helium gas, and copper foil electrode by applying RF high voltage. The atmospheric pressure plasma in the form of a bullet is released as a plume into the atmosphere. To study the properties of the plasma plume, the plasma plume current is estimated from the difference in currents on the circuit, and the drift velocity is measured using a photodetector. The relation of the plasma plume density n plu , which is estimated from the current and the drift velocity, and the gas flow velocity v gas is examined. It is found that the dependence of the density on the gas flow velocity has relations of n plu ∝ log(v gas ). However, the plasma plume density in the laminar flow is higher than that in the turbulent flow. Consequently, in the laminar flow, the density increases with increasing the gas flow velocity

  7. Process and device for decontamination of the waste gas of the fuel circuit of a fusion reactor from tritium and/or deuterium in waste gas containing them in chemically bound form

    International Nuclear Information System (INIS)

    Penzhorn, R.D.; Glugla, M.

    1987-01-01

    The invention concerns a process and a device for the decontamination of the wate gases of the fuel circuit of a fusion reactor from tritum and/or deuterium in waste gas containing them in chemically bound form, in which the waste gas is taken over an oxidation catalyst and then over a hot metal bed, tritium and/or deuterium is released from its compounds, separated from the waste gas and is returned to the fuel circuit. The process is intended to prevent losses of tritum and/or deuterium by permeation and the high loading of the hot metal getter materials, as occurs in the previously known corresponding process, and to avoid the formation of nitrogen oxides. This is achieved by: a) The catalytic oxidation reaction being carried out at a temperature of 200 0 C to 300 0 C. b) The gas mixture then being brought into contact with a hot metal bed at 200 0 C to 300 0 C to remove the remaining O 2 and for the selective conversion of the proportion of water into the hydrogen isotope. c) The gas mixture being brought into contact with a diaphragm made of palladium or a palladium-silver alloy at 400 0 C to 450 0 C to decompose the ammonia, all the released hydrogen isotope being passed through the diaphragm, separated from the remaining waste gas flow and removed. (orig.) [de

  8. HYLIFE-II tritium management system

    International Nuclear Information System (INIS)

    Longhurst, G.R.; Dolan, T.J.

    1993-06-01

    The tritium management system performs seven functions: (1) tritium gas removal from the blast chamber, (2) tritium removal from the Flibe, (3) tritium removal from helium sweep gas, (4) tritium removal from room air, (5) hydrogen isotope separation, (6) release of non-hazardous gases through the stack, (7) fixation and disposal of hazardous effluents. About 2 TBq/s (5 MCi/day) of tritium is bred in the Flibe (Li 2 BeF 4 ) molten salt coolant by neutron absorption. Tritium removal is accomplished by a two-stage vacuum disengager in each of three steam generator loops. Each stage consists of a spray of 0.4 mm diameter, hot Flibe droplets into a vacuum chamber 4 m in diameter and 7 m tall. As droplets fall downward into the vacuum, most of the tritium diffuses out and is pumped away. A fraction Φ∼10 -5 of the tritium remains in the Flibe as it leaves the second stage of the vacuum disengager, and about 24% of the remaining tritium penetrates through the steam generator tubes, per pass, so the net leakage into the steam system is about 4.7 MBq/s (11 Ci/day). The required Flibe pumping power for the vacuum disengager system is 6.6 MW. With Flibe primary coolant and a vacuum disengager, an intermediate coolant loop is not needed to prevent tritium from leaking into the steam system. An experiment is needed to demonstrate vacuum disengager operation with Flibe. A secondary containment shell with helium sweep gas captures the tritium permeating out of the Flibe ducts, limiting leaks there to about 1 Ci/day. The tritium inventory in the reactor is about 190 g, residing mostly in the large Flibe recirculation duct walls. The total cost of the tritium management system is 92 M$, of which the vacuum disengagers cost = 56%, the blast chamber vacuum system = 15%, the cryogenic plant = 9%, the emergency air cleanup and waste treatment systems each = 6%, the protium removal system = 3%, and the fuel storage system and inert gas system each = 2%

  9. Simulation study of intentional tritium release experiments in the caisson assembly for tritium safety at the TPL/JAERI

    International Nuclear Information System (INIS)

    Iwai, Y.; Hayashi, T.; Kobayashi, K.; Nishi, M.

    2001-01-01

    At the Tritium Process Laboratory (TPL) in Japan Atomic Energy Research Institute (JAERI), Caisson assembly for tritium safety study (CATS) with 12 m 3 of large airtight vessel (Caisson) was fabricated for confirmation and enhancement of fusion reactor safety to estimate the tritium behavior in the case, where the tritium leak accident should happen. One of the principal objectives of the present studies is the establishment of simulation method to predict the tritium behavior after the tritium leak accident should happen in a ventilated room. As for the understanding of initial tritium behavior until the tritium concentration become steady, the precise estimation of local flow rate in a room and time-dependent release behavior from the leak point are essential to predict the tritium behavior by simulation code. The three-dimensional eddy flow model considering, tritium-related phenomena was adopted to estimate the local flow rate in the 50 m 3 /h ventilated Caisson. The time-dependent tritium release behavior from the sample container was calculated by residence time distribution function. The calculated tritium concentrations were in good agreement with the experimental observations. The primary removal tritium behavior was also investigated by another code. Tritium gas concentrations decreased logarithmically to the time by ventilation. These observations were understandable by the reason that the flow in the ventilated Caisson was regarded as the perfectly mixing flow. The concentrations of tritiated water measured, and indications of tritium concentration by tritium monitors became gradually flat. This phenomena called 'tritium soaking effect' was found to be reasonably explained by considering the contribution of the exhaustion velocity by ventilation system, and the adsorption and desorption reaction rate of tritiated water on the wall material which is SUS 304. The calculated tritium concentrations were in good agreement with the experimental observations

  10. Modified Atmosphere Packaging of tomatoes; controlling gas and humidity

    NARCIS (Netherlands)

    Evelo, R.G.; Horst, J.

    1996-01-01

    Modified atmosphere (MA) packaging technology is a modern technique of which the application is steadily growing. Its essence is to reduce the decay of perishable produce by creating a special atmosphere around the produce. The MA factors influencing the quality behaviour of the produce are oxygen

  11. Atmospheric Gas-Phase Reactions of Fluorinated Compounds and Alkenes

    DEFF Research Database (Denmark)

    Østerstrøm, Freja From

    Experimental studies have been performed using three different smog chamber setups to investigate the atmospheric chemistry of fluorinated compounds as well as alkenes. The three instruments were at Ford Motor Company, USA, National Center for Atmospheric Research, USA, and Copenhagen Center...

  12. Mechanism of Runaway Electron Generation at Gas Pressures from a Few Atmospheres to Several Tens of Atmospheres

    Science.gov (United States)

    Zubarev, N. M.; Ivanov, S. N.

    2018-04-01

    The mechanism of runaway electron generation at gas pressures from a few atmospheres to several tens of atmospheres is proposed. According to this mechanism, the electrons pass into the runaway mode in the enhanced field zone that arises between a cathode micropoint—a source of field-emission electrons—and the region of the positive ion space charge accumulated near the cathode in the tails of the developing electron avalanches. As a result, volume gas ionization by runaway electrons begins with a time delay required for the formation of the enhanced field zone. This process determines the delay time of breakdown. The influence of the gas pressure on the formation dynamics of the space charge region is analyzed. At gas pressures of a few atmospheres, the space charge arises due to the avalanche multiplication of the very first field-emission electron, whereas at pressures of several tens of atmospheres, the space charge forms as a result of superposition of many electron avalanches with a relatively small number of charge carriers in each.

  13. Tritium dosimetry and standardization

    International Nuclear Information System (INIS)

    Balonov, M.I.

    1983-01-01

    Actual problem of radiation hygiene such as an evaluation of human irradiation hazard due to a contact with tritium compounds both in industrial and public spheres is under discussion. Sources of tritium release to environment are characterized. Methods of tritium radiation monitoring are discussed. Methods of dosimetry of internal human exposure resulted from tritium compounds are developed on the base of modern representations on metbolism and tritium radiobiological effect. A system of standardization of permissible intake of tritium compounds for personnel and persons of population is grounded. Some protection measures are proposed as applied to tritium overdosage

  14. Contribution to the dosimetry of tritium in the presence of inactive or active gases; Contribution a la dosimetrie du tritium en presence de gaz inactifs ou actifs

    Energy Technology Data Exchange (ETDEWEB)

    Soudain, G [Commissariat a l' Energie Atomique, Fontenay-aux-Roses (France). Centre d' Etudes Nucleaires

    1966-07-01

    Tritium is a dangerous gas for man and the maximum admissible doses in the atmosphere are sufficiently low for the dosage to be fairly difficult. We have developed an apparatus for measuring selectively the contamination of air by this gas when it is alone or when it is associated with other gaseous contaminants. The differential apparatus using two ionization chambers makes it possible to eliminate a parasitic {gamma} radiation field. In a few particular cases, the presence of the radio-active gas has been studied. From the practical point of view, the use of these chambers made of stainless steel makes for easier use since the problems connected with wall adsorption have been satisfactorily resolved. The method can be applied without restriction and very easily to the dosage of traces tritium in air or in the form of tritiated water or tritiated steam in the atmosphere. (author) [French] Le tritium est un gaz dangereux pour l'homme et les concentrations maximales admissibles dans l'atmosphere sont suffisamment basses pour que le dosage soit delicat. Nous avons etudie et realise un appareil qui permet de mesurer selectivement la contamination de l'air par ce gaz lorsqu'il est seul ou lorsqu'il est associe a d'autres agents gazeux contaminants. Le montage differentiel a deux chambres d'ionisation permet d'eliminer un champ de rayonnement {beta} parasite. Dans certains cas particuliers, la presence du gaz radioactif a ete etudiee. Sur le plan pratique, l'utilisation des chambres en acier inoxydable facilite les applications car les problemes d'adsorption aux parois ont ete bien resolus. La methode peut s'appliquer sans restriction et tres pratiquement au dosage des traces de tritium dans l'air ou encore sous forme d'eau tritiee ou de vapeur d'eau tritiee dans l'atmosphere. (auteur)

  15. Tritium in organic matter around Krsko Nuclear Power Plant

    International Nuclear Information System (INIS)

    Kristof, Romana; Zorko, Benjamin; Kozar Logar, Jasmina; Kosenina, Suzana

    2017-01-01

    The aim of the research was to obtain first results of tritium in the organic matter of environmental samples in the vicinity of Krsko NPP. The emphasis was on the layout of suitable sampling network of crops and fruits in nearby agricultural area. Method for determination of tritium in organic matter in the form of Tissue Free Water Tritium (TFWT) and Organically Bound Tritium (OBT) has been implemented. Capabilities of the methods were tested on real environmental samples and its findings were compared to modeled activities of tritium from atmospheric releases and literature based results of TFWT and OBT. (author)

  16. Harsh Environment Gas Sensor Array for Venus Atmospheric Measurements, Phase II

    Data.gov (United States)

    National Aeronautics and Space Administration — Makel Engineering and the Ohio State University propose to develop a harsh environment tolerant gas sensor array for atmospheric analysis in future Venus missions....

  17. Trace Atmospheric Gas Analyzer (TAGA) Dispersant Data for BP Spil/Deepwater Horizon - August 2010

    Data.gov (United States)

    U.S. Environmental Protection Agency — The Trace Atmospheric Gas Analyzer (TAGA) buses are self-contained mobile laboratories that conduct instant-result monitoring of air quality at particular locations....

  18. Protection of atmospheric air against radioactive gas and aerosol contaminants

    International Nuclear Information System (INIS)

    Zykova, A.S.

    1984-01-01

    Measures for contamination protection of atmospheric air subdivided into active and passive ones, are considered. The active measures envisage: development and application of waste-free flowsheets, use of flowsheets which restrict formation of gaseous-aerosol discharges; application of highly efficient treatment facilities torage. Dispersion of radioactive substances, released with discharges to the atmosphere, using high stacks; development of the corresponding site-selection solutions and arrangement of sanitary protective zones belong to passive measures. Measures for protection of atmospheric air also include waste and air contamination monitoring. The measures described are considered as applied to NPPs

  19. Removal and recovery of tritium from light and heavy water

    International Nuclear Information System (INIS)

    Butler, J.P.; Hammerli, M.

    1979-01-01

    A method and apparatus for removing tritium from light water are described, comprising contacting tritiated feed water in a catalyst column in countercurrent flow with hydrogen gas originating from an electrolysis cell so as to enrich this feed water with tritium from the electrolytic hydrogen gas and passing the tritium enriched water to an electrolysis cell wherein the electrolytic hydrogen gas is generated and then fed upwards through the catalyst column or recovered as product. The tritium content of the hydrogen gas leaving the top of the enricher catalyst column is further reduced in a stripper column containing catalyst which transfers the tritium to a countercurrent flow of liquid water. Anodic oxygen and water vapour from the anode compartment may be fed to a drier and condensed electrolyte recycled with a slip stream or recovered as a further tritium product stream. A similar method involving heavy water is also described. (author)

  20. Tritium accountancy

    International Nuclear Information System (INIS)

    Avenhaus, R.; Spannagel, G.

    1995-01-01

    Conventional accountancy means that for a given material balance area and a given interval of time the tritium balance is established so that at the end of that interval of time the book inventory is compared with the measured inventory. In this way, an optimal effectiveness of accountancy is achieved. However, there are still further objectives of accountancy, namely the timely detection of anomalies as well as the localization of anomalies in a major system. It can be shown that each of these objectives can be optimized only at the expense of the others. Recently, Near-Real-Time Accountancy procedures have been studied; their methodological background as well as their merits will be discussed. (orig.)

  1. Tritium Management Loop Design Status

    Energy Technology Data Exchange (ETDEWEB)

    Rader, Jordan D. [ORNL; Felde, David K. [ORNL; McFarlane, Joanna [ORNL; Greenwood, Michael Scott [ORNL; Qualls, A L. [ORNL; Calderoni, Pattrick [Idaho National Laboratory (INL)

    2017-12-01

    This report summarizes physical, chemical, and engineering analyses that have been done to support the development of a test loop to study tritium migration in 2LiF-BeF2 salts. The loop will operate under turbulent flow and a schematic of the apparatus has been used to develop a model in Mathcad to suggest flow parameters that should be targeted in loop operation. The introduction of tritium into the loop has been discussed as well as various means to capture or divert the tritium from egress through a test assembly. Permeation was calculated starting with a Modelica model for a transport through a nickel window into a vacuum, and modifying it for a FLiBe system with an argon sweep gas on the downstream side of the permeation interface. Results suggest that tritium removal with a simple tubular permeation device will occur readily. Although this system is idealized, it suggests that rapid measurement capability in the loop may be necessary to study and understand tritium removal from the system.

  2. TRIO-01 experiment: in-situ tritium-recovery results

    International Nuclear Information System (INIS)

    Clemmer, R.G.; Finn, P.A.; Billone, M.C.

    1983-08-01

    The TRIO-01 experiment is a test of in-situ tritium recovery from γ-LiAlO 2 with test conditions chosen to simulate those anticipated in fusion power reactors. A status report is presented which describes qualitatively the results observed during the irradiation phase of the experiment. Both the rate of tritium release and the chemical forms of tritium were measured using a helium sweep gas which flowed past the breeder material to a gas analysis system

  3. TRIO-01 experiment: in-situ tritium recovery results

    International Nuclear Information System (INIS)

    Clemmer, R.G.; Finn, P.A.; Billone, M.C.

    1983-10-01

    The TRIO-01 experiment is a test of in-situ tritium recovery from γ-LiAlO 2 with test conditions chosen to simulate those anticipated in fusion power reactors. A status report is presented which describes qualitatively the results observed during the irradiation phase of the experiment. Both the rate of tritium release and the chemical forms of tritium were measured using a helium sweep gas which flowed past the breeder material to a gas analysis system

  4. Breeding blanket development. Tritium release from breeder

    International Nuclear Information System (INIS)

    Tsuchiya, Kunihiko; Kawamura, Hiroshi; Nagao, Yoshiharu

    2006-01-01

    Engineering data on neutron irradiation performance of tritium breeders are needed to design the breeding blanket of fusion reactor. In this study, tritium release experiments of the breeders were carried out to examine the effects of various parameters (such as sweep gas flow rate, hydrogen content in sweep gas, irradiation temperature and thermal neutron flux) on tritium generation and release behavior. Lithium titanate (Li 2 TiO 3 ) is considered as a candidate tritium breeder in the blanket design of International Thermonuclear Experimental Reactor (ITER). As for the shape of the breeder material, a small spherical form is preferred to reduce the thermal stress induced in the breeder. Li 2 TiO 3 pebbles of about 170g in total weight and with 0.3 and 2 mm in diameter were manufactured by a wet process, and an assembly packed with the binary Li 2 TiO 3 pebbles was irradiated in Japan Materials Testing Reactor (JMTR). The tritium was generated in the Li 2 TiO 3 pebble bed and released from the pebble bed, and was swept downstream using the sweep gas for on-line analysis of tritium content. Concentration of total tritium and gaseous tritium (HT or T 2 gas) released from the Li 2 TiO 3 pebble bed were measured by ionization chambers, and the ratio of (gaseous tritium)/(total tritium) was evaluated. The sweep gas flow rate was changed from 100 to 900cm 3 /min, and hydrogen content in the sweep gas was changed from 100 to 10000 ppm. Furthermore, thermal neutron flux was changed using a window made of hafnium (Hf) neutron absorber. The irradiation temperature at an outer region of the Li 2 TiO 3 pebble bed was held between 200 and 400degC. The main results of this experiment are summarized as follows. 1) When the temperature at the outside edge of the Li 2 TiO 3 pebble bed exceeded 100degC, the tritium release from the Li 2 TiO 3 pebble bed started. The ratio of the tritium release rate and the tritium generation rate (normalized tritium release rate: R/G) reached

  5. Gas phase hydrogen peroxide production in atmospheric pressure glow discharges operating in He - H2O

    NARCIS (Netherlands)

    Vasko, C.A.; Veldhuizen, van E.M.; Bruggeman, P.J.

    2013-01-01

    The gas phase production of hydrogen peroxide (H2O2) in a RF atmospheric pressure glow discharge with helium and water vapour has been investigated as a function of the gas flow. It is shown that the production of H2O2 is through the recombination of two OH radicals in a three body collision and the

  6. Tritium means of detection and of protection

    International Nuclear Information System (INIS)

    Sutra-Fourcade, Y.

    1967-01-01

    The report is an attempt to correlate present data concerning tritium, especially from the health physics points of view. The various detection and measurement methods are reviewed in turn: measurement of tritium in the atmosphere, in liquids and on surfaces. The operation of various types of apparatus is analyzed and the sensitivity limits deduced from laboratory tests are given. Otter sections are devoted to the means of protection which can be used against inhalation of tritium (ventilation, protective clothing) and to calculations of the changes in atmospheric pollution in a given place and of the time spent in a contaminated zone. The last part deals with the decontamination of equipment contaminated with tritium. (author) [fr

  7. The tritium and the controlled fusion reactors

    International Nuclear Information System (INIS)

    Leger, D.; Rouyer, J.L.

    1986-04-01

    It is shown how tritium is used how it is circulating in a fusion reactor. The great functions of tritium circuits are detailed: reprocessing of burnt gases, reprocessing of gases coming from neutral injectors, reprocessing from gaseous wastes, detritiation of cooling fluids. Current technologic developments are quoted. Then tritium confinement and containment, in normal or accidental situations, are displayed. Limitation devices of effluents and release for normal operating (noticeably the reprocessing systems of atmosphere) and safety and protection systems in case of accident are described [fr

  8. Management of Tritium in European Spallation Source

    DEFF Research Database (Denmark)

    Ene, Daniela; Andersson, Kasper Grann; Jensen, Mikael

    2015-01-01

    with the country regulation criteria. The aim of this paper is to give an overview of the different aspects of the tritium management in ESS facility. Besides the design parameter study of the helium coolant purification system of the target the consequences of the tritium releasing into the environment were also...... of the results on soil examinations. With the assumption of 100% release of tritium to the atmosphere during the occurring of the extreme accidents, it was found as well that the total dose complies with the constraint....

  9. Elemental tritium deposition and conversion in the terrestrial environment

    International Nuclear Information System (INIS)

    Dunstall, T.G.; Ogram, G.L.; Spencer, F.S.

    1985-01-01

    Studies were undertaken to determine the deposition and conversion of atmospheric elemental tritium in soils and vegetation. In the field tritium deposition velocities ranged between 0.007 and 0.07 cm s -1 during the summer and autumn and were less than 0.0005 cm s -1 during the winter. Deposition velocity was found to depend significantly on soil water content, total pore space and organic content in controlled laboratory experiments. In contrast to soils, exposure of vegetation to atmospheric elemental tritium resulted in negligible uptake and conversion in foliage. These studies are of significance to the assessment of behaviour and impact of elemental tritium releases

  10. Tritium-containment systems: a tradeoff study

    International Nuclear Information System (INIS)

    Folkers, C.L.; Cena, R.J.

    1978-01-01

    Various design parameters are evaluated that affect the performance of tritium-containment systems for fusion reactors. Our study included a review of such parameters as tritium forms, impurities, catalysts, adsorbents, getters, and as low as reasonably achievable principles. We organized these schemes, which can be considered for treating either air or inert atmospheres, so one could easily make orderly choices and tradeoffs for optimum performance. The relationships examined involved purification-system decontamination factors, flow rates, recycling and leakage, and environmental losses

  11. Permafrost-associated gas hydrates of Northern Alaska: A possible source of atmospheric methane

    International Nuclear Information System (INIS)

    Collett, T.S.

    1991-01-01

    Numerous researchers have suggested that destabilized gas hydrates may be contributing to this buildup in atmospheric methane. Little is known about the geologic or geochemical nature of gas hydrates, even though they are known to occur in numerous arctic sedimentary basins. Because of the abundance of available geologic data, the author's research has focused on assessing the distribution of gas hydrates within the onshore regions of northern Alaska; currently, onshore permafrost-associated gas hydrates are believed to be insulated from most atmospheric temperature changes and are not at this time an important source of atmospheric methane. Their onshore gas hydrate studies, however, can be used to develop geologic analogs for potential gas hydrate occurrences within unexplored areas, such as the thermally unstable nearshore continental shelf. On the North Slope, gas hydrates have been identified in 36 industry wells by using well-log responses calibrated to the response of an interval in one well where gas hydrates were recovered in a core by an oil company. Most gas hydrates they identified occur in six laterally continuous Upper Cretaceous and lower Tertiary sandstone and conglomerate units; all these hydrates are geographically restricted to the area overlying the eastern part of the Kuparuk River Oil Field and the western part of the Prudhoe Bay Oil Field. Stable carbon isotope geochemical analysis of well cuttings suggests that the identified hydrates originated from a mixture of deep-source thermogenic gas and shallow microbial gas that was either directly converted to gas hydrate or first concentrated in existing traps and later converted to gas hydrate. They postulate that the thermogenic gas migrated from deeper reservoirs along the faults thought to be migration pathways for the large volumes of shallow, heavy oil found in the same area

  12. Contamination mechanisms of air basin with tritium in venues of underground nuclear explosions at the former Semipalatinsk test site

    International Nuclear Information System (INIS)

    Lyakhova, O.N.; Lukashenko, S.N.; Larionova, N.V.; Tur, Y.S.

    2012-01-01

    During the period of testing from 1945 to 1962 at the territory of Semipalatinsk test site (STS) within the Degelen Mountains in tunnels, 209 underground nuclear explosions were produced. Many of the tunnels have seasonal water seepage in the form of streams, through which tritium migrates from the underground nuclear explosion (UNE) venues towards the surface. The issue of tritium contamination occupies a special place in the radioactive contamination of the environment. In this paper we assess the level and distribution of tritium in the atmospheric air of ecosystems with water seepage at tunnels № 176 and № 177, located on “Degelen” site. There has been presented general nature of tritium distribution in the atmosphere relative to surface of a watercourse which has been contaminated with tritium. The basic mechanisms were studied for tritium distribution in the air of studied ecosystems, namely, the distribution of tritium in the systems: water–atmosphere, tunnel air–atmosphere, soil water–atmosphere, vegetation–atmosphere. An analytical calculation of tritium concentration in the atmosphere by the concentration of tritium in water has been performed. There has experimentally obtained the dependence for predictive assessment of tritium concentrations in air as a function of tritium concentration in one of the inlet sources such as water, tunnel air, soil water, vegetation, etc.. The paper also describes the general nature of tritium distribution in the air in the area “Degelen”. - Highlights: ► The basic mechanisms for tritium distribution in the air of nuclear testing sites were examined. ► We researched the distribution of tritium in the systems such as water–atmosphere, tunnel air–atmosphere, soil water–atmosphere and vegetation–atmosphere. ► An analytical calculation of tritium concentration in the atmosphere was performed. ► We experimentally obtained the dependence for predictive assessment of tritium concentrations in

  13. Separation of tritium from gaseous and aqueous effluent systems

    International Nuclear Information System (INIS)

    Kobisk, E.H.

    1977-01-01

    Three processes are discussed for separating tritium from gaseous and aqueous effluent systems: separation in the gas phase using Pd-25 wt percent Ag alloy diffusion membranes; electrolytic separation in the aqueous phase using ''bipolar'' electrodes; and the countercurrent exchange of tritium-containing hydrogen gas with water on catalytic surfaces combined with separation by direct electrolysis

  14. The operation of the Tokamak Fusion Test Reactor Tritium Facility

    International Nuclear Information System (INIS)

    Gentile, C.A.; LaMarche, P.H.

    1995-01-01

    The TFTR tritium operations staff has successfully received, stored, handled, and processed over five hundred thousand curies of tritium for the purpose of supporting D-T (Deuterium-Tritium) operations at TFTR. Tritium operations personnel nominally provide continuous round the clock coverage (24 hours/day, 7 days/week) in shift complements consisting of I supervisor and 3 operators. Tritium Shift Supervisors and operators are required to have 5 years of operational experience in either the nuclear or chemical industry and to become certified for their positions. The certification program provides formal instruction, as well as on the job training. The certification process requires 4 to 6 months to complete, which includes an oral board lasting up to 4 hours at which time the candidate is tested on their knowledge of Tritium Technology and TFTR Tritium systems. Once an operator is certified, the training process continues with scheduled training weeks occurring once every 5 weeks. During D-T operations at TFTR the operators must evacuate the tritium area due to direct radiation from TFTR D-T pulses. During '' time operators maintain cognizance over tritium systems via a real time TV camera system. Operators are able to gain access to the Tritium area between TFTR D-T pulses, but have been excluded from die tritium area during D-T pulsing for periods up to 30 minutes. Tritium operators are responsible for delivering tritium gas to TFRR as well as processing plasma exhaust gases which lead to the deposition of tritium oxide on disposable molecular sieve beds (DMSB). Once a DMSB is loaded, the operations staff remove the expended DMSB, and replace it with a new DMSB container. The TFIR tritium system is operated via detailed procedures which require operator sign off for system manipulation. There are >300 procedures controlling the operation of the tritium systems

  15. Thermochromatography study of volatile polonium species in various gas atmospheres

    CERN Document Server

    Maugeri, Emilio Andrea; Eichler, Robert; Piguet,David; Mendonça, Tania Melo; Stora, Thierry; Schumann, Dorothea

    2014-01-01

    Phenomena related to the volatilization of polonium and its compounds are critical issues for the safety assessment of the innovative lead–bismuth cooled type of nuclear reactor or accelerator driven systems. The formation and volatilization of different species of polonium and their interaction with fused silica was studied by thermochromatography using carrier gases with varied redox potential. The obtained results show that under inert and reducing conditions in the absence of moisture, elemental polonium is formed. Polonium compounds more volatile than elemental polonium can be formed if traces of moisture are present in both inert and reducing carrier gas. The use of dried oxygen as carrier gas leads to the formation of polonium oxides, which are less volatile than elemental polonium. It was also found that the volatility of polonium oxides increases with increasing oxidation state. In the presence of moisture in an oxidizing carrier gas, species are formed that are more volatile than the oxides and le...

  16. Conceptual design of an emergency tritium clean-up system

    International Nuclear Information System (INIS)

    Muller, M.E.

    1978-01-01

    The Los Alamos Scientific Laboratory (LASL) has been selected by the Department of Energy (DOE) to design, build, and operate a facility to demonstrate the operability of the tritium-related subsystems that would be required to successfully develop fusion reactor systems. An emergency tritium clean-up subsystem (ETC) for this facility will be designed to remove tritium from the cell atmosphere if an accident causes the primary and secondary tritium containment to be breached. Conceptually, the ETC will process cell air at the rate of 0.65 actual m 3 /s and will achieve an overall decontamination factor of 10 6 per tritium oxide (T 2 O). Following the maximum credible release of 100 g of tritium, the ETC will restore the cell to opertional status within 24 h without a significant release of tritium to the environment

  17. A model for global cycling of tritium

    International Nuclear Information System (INIS)

    Killough, G.G.; Kocher, D.C.

    1988-01-01

    Dynamic compartment models are widely used to describe global cycling of radionuclides for purposes of dose estimation. In this paper the authors present a new global tritium model that reproduces environmental time-series data on concentrations in precipitation, ocean surface waters, and surface fresh waters in the northern hemisphere, concentrations of atmospheric tritium in the southern hemisphere, and the latitude dependence of tritium in both hemispheres. Names TRICYCLE (for TRItium CYCLE) the model is based on the global hydrologic cycle and includes hemispheric stratospheric compartments, disaggregation of the troposphere and ocean surface waters into eight latitude zones, consideration of the different concentrations of atmospheric tritium over land and over the ocean, and a diffusive model for transport in the ocean. TRICYCLE reproduces the environmental data if it is assumed that about 50% of the tritium from atmospheric weapons testing was injected directly into the northern stratosphere as HTO. The model's latitudinal disaggregation permits taking into account the distribution of population. For a uniformly distributed release of HTO into the worldwide troposphere, TRICYCLE predicts a collective dose commitment to the world population that exceeds the NCRP model's corresponding prediction by a factor of three

  18. A model for global cycling of tritium

    International Nuclear Information System (INIS)

    Killough, G.G.; Kocher, D.C.

    1988-01-01

    Dynamic compartment models are widely used to describe global cycling of radionuclides for purposes of dose estimation. In this paper, we present a new global tritium model that reproduces environmental time-series data on concentrations in precipitation, ocean surface waters, and surface fresh waters in the northern hemisphere, concentrations of atmospheric tritium in the soutehrn hemisphere, and the latitude dependence of tritium in both hemispheres. Named TRICYCLE for Tritium CYCLE, the model is based on the global hydrologic cycle and includes hemisphereic stratospheric compartments, disaggregation of the troposphere and ocean surface waters into eight latitudezones, consideration of the different concentrations of atmospheric tritium over land and over the ocean, and a diffusive model for transport in the ocean. TRICYCLE reproduces the environmental data if we assume that about 50% of the tritium from atmospheric weapons testing was injected directly into the northern stratosphere as HTO. The models latitudinal disaggregation permits taking into account the distribution of population. For a unfiormaly distributed release of HTO into the worldwide troposphere, TRICYCLE predicts a collective dose commitment to the world population that exceeds the corresponding prediction by the NCRP model by about a factor of 3. 11 refs., 5 figs., 1 tab

  19. Kinetics of catalyzed tritium oxidation in air at ambient temperature

    International Nuclear Information System (INIS)

    Sherwood, A.E.

    1980-01-01

    Tritium/air oxidation kinetic data are derived from measurements carried out with three catalysts. All experiments were carried out at room temperature - a regime that provides a severe test for catalyst effectiveness. Each catalyst consists of a high-surface-area substrate in pelletized form, onto which precious metal has been dispersed. The metal/substrate combinations investigated are: platinum/alumina, palladium/kaolin, and paladium/zeolite. Each of the dispersed-metal catalysts is extremely effective in promoting tritium oxidation in comparison with self-catalyzed atmospheric conversion; equivalent first-order rate constants are higher by roughly nine orders of magnitude. Electron-microprobe scans reveal that the dispersed metal is deposited near the outer surface of the catalyst, with metal concentration decreasing exponentially from the pellet surface. The platinum-based catalyst is more effective than the palladium catalysts on a surface-area basis by about a factor of three. Rate coefficients are determined from concentration decay following a spike injection of tritium into an air-filled enclosure processed by recirculation through an oxidation/adsorption system. The catalytic reaction is first-order in tritium concentration in the range 10 to 10 5 μCi/m 3 (4 ppt-40 ppB). Addition of hydrogen carrier gas is unnecessary. Catalytic activity for all three catalysts declines with time of exposure to air after activation, following a power-law decay with an exponent of -1/2. Reactivation with hot hydrogen gas effectively restores initial catalytic activity

  20. Technical solutions for tritium removal from Cernavoda NPP heavy water systems

    International Nuclear Information System (INIS)

    Barariu, Gheorghe; Panait, Adrian

    2002-01-01

    In CANDU nuclear plants 2400 KCi/GW(e) - year tritium is generated. At a CANDU - 600 reactor similar to Cernavoda NPP Unit 1, 1500 KCi/year of tritium is generated 95% being in the D 2 O moderator, which can achieve a radioactivity level of 80 - 100 Ci/kg. Tritium in heavy water contributes with 30 - 50% to the doses received by operation personnel and with 20% to the radioactivity released to the environment. The extraction of tritium heavy water at CANDU reactors implies the following possibilities: - the radioactivity level reduction in the operation area; - the maintenance and repair cost reduction due to reduction of personnel protection measures and increased labor productivity; - the increase of NPP utilization factor by shutdown time reduction for maintenance and repair; - tritium concentration reduction from technological systems, ensuring thus the possibility of redesigning the systems in order to lower the cost of investment; - profitable use of extracted tritium. Technical measures provided by AECL project for CANDU 600 at Cernavoda make possible to satisfy the current standards concerning tritium concentration in the operation area atmosphere of 5 x 10 -6 Ci/m 3 . The regulations recommend that the radioactivity level should be maintained as low as possible in conformity with ALARA principles. Also, it is possible that norms will become more restrictive in the future, so the tritium removal technology is a good preventive measure which may become very necessary. The methods, which currently reached the industrial or pilot stages, are based on catalyzed chemical exchange, the heavy water electrolysis, and deuterium distillation. They are known as: VPCE - Vapour Phase Catalytic Exchange; LPCE - Liquid Phase Catalytic Exchange; DE - Direct Electrolysis; CD - Cryogenic Distillation. As transfer processes the catalyzed chemical exchange and heavy water electrolysis are used while concentration of tritium gas is done by cryogenic distillation. At present the

  1. Tritium behaviour in ceramic breeder blankets

    International Nuclear Information System (INIS)

    Miller, J.M.

    1989-01-01

    Tritium release from the candidate ceramic materials, Li 2 O, LiA10 2 , Li 2 SiO 3 , Li 4 SiO 4 and Li 2 ZrO 3 , is being investigated in many blanket programs. Factors that affect tritium release from the ceramic into the helium sweep gas stream include operating temperature, ceramic microstructure, tritium transport and solubility in the solid. A review is presented of the material properties studied and of the irradiation programs and the results are summarized. The ceramic breeder blanket concept is briefly reviewed

  2. STAR facility tritium accountancy

    International Nuclear Information System (INIS)

    Pawelko, R. J.; Sharpe, J. P.; Denny, B. J.

    2008-01-01

    The Safety and Tritium Applied Research (STAR) facility has been established to provide a laboratory infrastructure for the fusion community to study tritium science associated with the development of safe fusion energy and other technologies. STAR is a radiological facility with an administrative total tritium inventory limit of 1.5 g (14,429 Ci) [1]. Research studies with moderate tritium quantities and various radionuclides are performed in STAR. Successful operation of the STAR facility requires the ability to receive, inventory, store, dispense tritium to experiments, and to dispose of tritiated waste while accurately monitoring the tritium inventory in the facility. This paper describes tritium accountancy in the STAR facility. A primary accountancy instrument is the tritium Storage and Assay System (SAS): a system designed to receive, assay, store, and dispense tritium to experiments. Presented are the methods used to calibrate and operate the SAS. Accountancy processes utilizing the Tritium Cleanup System (TCS), and the Stack Tritium Monitoring System (STMS) are also discussed. Also presented are the equations used to quantify the amount of tritium being received into the facility, transferred to experiments, and removed from the facility. Finally, the STAR tritium accountability database is discussed. (authors)

  3. Tritium proof-of-principle injector experiment

    International Nuclear Information System (INIS)

    Fisher, P.W.; Milora, S.L.; Combs, S.K.; Carlson, R.V.; Coffin, D.O.

    1988-01-01

    The Tritium Proof-of-Principle (TPOP) pellet injector was designed and built by Oak Ridge National Laboratory (ORNL) to evaluate the production and acceleration of tritium pellets for fueling future fision reactors. The injector uses the pipe-gun concept to form pellets directly in a short liquid-helium-cooled section of the barrel. Pellets are accelerated by using high-pressure hydrogen supplied from a fast solenoid valve. A versatile, tritium-compatible gas-handling system provides all of the functions needed to operate the gun, including feed gas pressure control and flow control, plus helium separation and preparation of mixtures. These systems are contained in a glovebox for secondary containment of tritium Systems Test Assembly (TSTA) at Los Alamos National Laboratory (LANL). 18 refs., 3 figs

  4. Gas Leak Detection by Dilution of Atmospheric Oxygen

    Directory of Open Access Journals (Sweden)

    Armin Lambrecht

    2017-12-01

    Full Text Available Gas leak detection is an important issue in infrastructure monitoring and industrial production. In this context, infrared (IR absorption spectroscopy is a major measurement method. It can be applied in an extractive or remote detection scheme. Tunable laser spectroscopy (TLS instruments are able to detect CH4 leaks with column densities below 10 ppm·m from a distance of 30 m in less than a second. However, leak detection of non-IR absorbing gases such as N2 is not possible in this manner. Due to the fact that any leaking gas displaces or dilutes the surrounding background gas, an indirect detection is still possible. It is shown by sensitive TLS measurements of the ambient background concentration of O2 that N2 leaks can be localized with extractive and standoff methods for distances below 1 m. Minimum leak rates of 0.1 mbar·L/s were determined. Flow simulations confirm that the leakage gas typically effuses in a narrow jet. The sensitivity is mainly determined by ambient flow conditions. Compared to TLS detection of CH4 at 1651 nm, the indirect method using O2 at 761 nm is experimentally found to be less sensitive by a factor of 100. However, the well-established TLS of O2 may become a universal tool for rapid leakage screening of vessels that contain unknown or inexpensive gases, such as N2.

  5. Development of a compact tritium activity monitor and first tritium measurements

    Energy Technology Data Exchange (ETDEWEB)

    Röllig, M., E-mail: marco.roellig@kit.edu; Ebenhöch, S.; Niemes, S.; Priester, F.; Sturm, M.

    2015-11-15

    Highlights: • We report about experimental results of a new tritium activity monitoring system using the BIXS method. • The system is compact and easy to implement. It has a small dead volume of about 28 cm{sup 3} and can be used in a flow-through mode. • Gold coated surfaces are used to improve significantly count rate stability of the system and to reduce stored inventory. - Abstract: To develop a convenient tool for in-line tritium gas monitoring, the TRitium Activity Chamber Experiment (TRACE) was built and commissioned at the Tritium Laboratory Karlsruhe (TLK). The detection system is based on beta-induced X-ray spectrometry (BIXS), which observes the bremsstrahlung X-rays generated by tritium decay electrons in a gold layer. The setup features a measuring chamber with a gold-coated beryllium window and a silicon drift detector. Such a detection system can be used for accountancy and process control in tritium processing facilities like the Karlsruhe Tritium Neutrino Experiment (KATRIN). First characterization measurements with tritium were performed. The system demonstrates a linear response between tritium partial pressure and the integral count rate in a pressure range of 1 Pa up to 60 Pa. Within 100 s measurement time the lower detection limit for tritium is (143.63 ± 5.06) · 10{sup 4} Bq. The system stability of TRACE is limited by a linear decrease of integral count rate of 0.041 %/h. This decrease is most probably due to exchange interactions between tritium and the stainless steel walls. By reducing the interaction surface with stainless steel, the decrease of the integral count rate was reduced to 0.008 %/h. Based on the first results shown in this paper it can be concluded that TRACE is a promising complement to existing tritium monitoring tools.

  6. ENSO Atmospheric Teleconnections and Their Response to Greenhouse Gas Forcing

    Science.gov (United States)

    Yeh, Sang-Wook; Cai, Wenju; Min, Seung-Ki; McPhaden, Michael J.; Dommenget, Dietmar; Dewitte, Boris; Collins, Matthew; Ashok, Karumuri; An, Soon-Il; Yim, Bo-Young; Kug, Jong-Seong

    2018-03-01

    El Niño and Southern Oscillation (ENSO) is the most prominent year-to-year climate fluctuation on Earth, alternating between anomalously warm (El Niño) and cold (La Niña) sea surface temperature (SST) conditions in the tropical Pacific. ENSO exerts its impacts on remote regions of the globe through atmospheric teleconnections, affecting extreme weather events worldwide. However, these teleconnections are inherently nonlinear and sensitive to ENSO SST anomaly patterns and amplitudes. In addition, teleconnections are modulated by variability in the oceanic and atmopsheric mean state outside the tropics and by land and sea ice extent. The character of ENSO as well as the ocean mean state have changed since the 1990s, which might be due to either natural variability or anthropogenic forcing, or their combined influences. This has resulted in changes in ENSO atmospheric teleconnections in terms of precipitation and temperature in various parts of the globe. In addition, changes in ENSO teleconnection patterns have affected their predictability and the statistics of extreme events. However, the short observational record does not allow us to clearly distinguish which changes are robust and which are not. Climate models suggest that ENSO teleconnections will change because the mean atmospheric circulation will change due to anthropogenic forcing in the 21st century, which is independent of whether ENSO properties change or not. However, future ENSO teleconnection changes do not currently show strong intermodel agreement from region to region, highlighting the importance of identifying factors that affect uncertainty in future model projections.

  7. Effects of atmospheric gas composition and temperature on the gasification of coal in hot briquetting carbon composite iron ore

    Energy Technology Data Exchange (ETDEWEB)

    Ueki, Y.; Kanayama, M.; Maeda, T.; Nishika, K.; Shimizu, M. [Kyushu University, Fukuoka (Japan). Dept. of Materials Science & Engineering

    2007-01-15

    The gasification behavior of carbon composite iron ore produced by hot briquetting process was examined under various gas atmospheres such as CO-N{sub 2}, CO{sub 2}-N, and CO-CO{sub 2} at various temperatures. The gasification of coal was affected strongly by atmospheric gas concentration and reaction temperature. Kinetic analysis in various gas atmospheres was carried out by using the first order reaction model, which yields the straight line relation between reaction rate constants for the gasification of coal and the gas concentration. Therefore, reaction rate constants for the gasification of coal in CO-CO{sub 2}-N{sub 2} gas atmosphere were derived.

  8. Effect of feed-gas humidity on nitrogen atmospheric-pressure plasma jet for biological applications.

    Science.gov (United States)

    Stephan, Karl D; McLean, Robert J C; DeLeon, Gian; Melnikov, Vadim

    2016-11-14

    We investigate the effect of feed-gas humidity on the oxidative properties of an atmospheric-pressure plasma jet using nitrogen gas. Plasma jets operating at atmospheric pressure are finding uses in medical and biological settings for sterilization and other applications involving oxidative stress applied to organisms. Most jets use noble gases, but some researchers use less expensive nitrogen gas. The feed-gas water content (humidity) has been found to influence the performance of noble-gas plasma jets, but has not yet been systematically investigated for jets using nitrogen gas. Low-humidity and high-humidity feed gases were used in a nitrogen plasma jet, and the oxidation effect of the jet was measured quantitatively using a chemical dosimeter known as FBX (ferrous sulfate-benzoic acid-xylenol orange). The plasma jet using high humidity was found to have about ten times the oxidation effect of the low-humidity jet, as measured by comparison with the addition of measured amounts of hydrogen peroxide to the FBX dosimeter. Atmospheric-pressure plasma jets using nitrogen as a feed gas have a greater oxidizing effect with a high level of humidity added to the feed gas.

  9. Evaluation of permeable and non-permeable tritium in normal condition in a fusion reactor

    Energy Technology Data Exchange (ETDEWEB)

    Marta, V; Manuel, P J [Instituto de Fusion Nuclear (DENIM)/ETSII, Universidad Politecnica Madrid (UPM) (Spain); Sedano Luis, A [Ministerio de Educacion y Ciencia, Ciemat (Spain)], E-mail: marta@denim.upm.es

    2008-05-15

    The tritium cycle, technologies of process and control of the tritium in the plant will constitute a fraction of the environmental impact of the first generation of DT fusion reactors. The efforts of conceptual development of the tritium cycle are centered in the Internal Regenerator Cycle. The tritium could be recovered from a flow of He gas, or directly from solid breeder. The limits of transfers to the atmosphere are assumed {approx} 1 gr-T/a ({approx}20 Ci/a) (without species distinction). In the case of ITER, for example, we have global demands of control of 5 orders of magnitude have been demonstrated at experimental level. The transfer limits determine the key parameters in tritium Cycle (HT, HTO, as dominant, and T2, T2O as marginal). Presently, the transfer from the cycle to the environment is assumed through the exchange system of the power plant (primary to secondary). That transport is due to the permeation through HT, T2, or leakage to the coolant in the primary system. It is key the chemical optimization in the primary system, that needs to be reanalyzed in terms of radiological impact both for permeable, HT, T2, and non-permeable HTO, T2O. It is necessary considered the pathway of tritium from the reactor to the atmosphere, these processes are modelled adequately. Results of the assessments were early and chronic doses which have been evaluated for the Most Exposed Individual at particular distance bands from the release point. The impact evaluations will be performed with the computational tools (NORMTRI), besides national regulatory models, internationally accepted computer these code for dosimetric evaluations of tritiated effluents in operational conditions.

  10. Preparation of pyronaridine labelled with tritium

    International Nuclear Information System (INIS)

    Jiang Shangen; Zhang Liufang; Zheng Dongzhu; Feng Zheng; Wu Zufan

    1987-01-01

    Pyronaridine is a high efficient and low toxic new antimalarial drug. 3 H-pyronaridine was prepared by catalytic isotopic exchange in solution with tritium gas using PdO/BaSO 4 as catalyst. That crude product was purified by extraction. 3 H-NMR spectra of pyronaridine showed that tritium was labelled at the 6-position. Specific activity of 3 H-pyronaridine was 5.5 Ci/mmol and radiochemical purity over 95%

  11. Preparation of pyronaridine labelled with tritium

    Energy Technology Data Exchange (ETDEWEB)

    Shangen, Jiang; Liufang, Zhang; Dongzhu, Zheng; Zheng, Feng; Zufan, Wu

    1987-12-01

    Pyronaridine is a high efficient and low toxic new antimalarial drug. /sup 3/H-pyronaridine was prepared by catalytic isotopic exchange in solution with tritium gas using PdO/BaSO/sub 4/ as catalyst. That crude product was purified by extraction. /sup 3/H-NMR spectra of pyronaridine showed that tritium was labelled at the 6-position. Specific activity of /sup 3/H-pyronaridine was 5.5 Ci/mmol and radiochemical purity over 95%.

  12. Atmospheric pulsed laser deposition of plasmonic nanoparticle films of silver with flowing gas and flowing atmospheric plasma

    Science.gov (United States)

    Khan, T. M.; Pokle, A.; Lunney, J. G.

    2018-04-01

    Two methods of atmospheric pulsed laser deposition of plasmonic nanoparticle films of silver are described. In both methods the ablation plume, produced by a 248 nm, 20 ns excimer laser in gas, is strongly confined near the target and forms a nanoparticle aerosol. For both the flowing gas, and the atmospheric plasma from a dielectric barrier discharge plasma source, the aerosol is entrained in the flow and carried to a substrate for deposition. The nanoparticle films produced by both methods were examined by electron microscopy and optical absorption spectroscopy. With plasma assistance, the deposition rate was significantly enhanced and the film morphology altered. With argon gas, isolated nanoparticles of 20 nm size were obtained, whereas in argon plasma, the nanoparticles are aggregated in clusters of 90 nm size. Helium gas also leads to the deposition of isolated nanoparticles, but with helium plasma, two populations of nanoparticles are observed: one of rounded particles with a mean size of 26 nm and the other of faceted particles with a mean size 165 nm.

  13. Noble gas atmospheric monitoring for international safeguards at reprocessing plants

    International Nuclear Information System (INIS)

    Nakhleh, C.W.; Poths, J.; Stanbro, W.D.; Perry, R.T. Jr.; Wilson, W.B.; Fearey, B.L.

    1997-01-01

    The use of environmental sampling is a major component of the improvements of International Atomic Energy Agency safeguards being carried out under Program 93+2. Nonradioactive noble gas isotopic measurements in the effluent stream of large reprocessing facilities may provide useful confirmatory information on the burnup and reactor type of the spent fuel undergoing reprocessing. The authors have taken and analyzed stack samples at an operating facility. The data show clear fission signals. The authors are currently applying a maximum-likelihood estimation procedure to determine the fuel burnup from these data. They anticipate that the general features involved in the table noble gas problem--selection of appropriate signals, measurement of those signals under realistic conditions, and inverse calculation of parameters of interest from the environmental data--will be present in all environmental sampling problems. These methods should therefore be widely applicable

  14. Issues Associated with Tritium Legacy Materials

    International Nuclear Information System (INIS)

    Mills, Michael

    2008-01-01

    This paper highlights some of the issues associated with the treatment of legacy materials linked to research into tritium over many years and also of materials used to contain or store tritium. The aim of the work is to recover tritium where practicable, and to leave the residual materials passively safe, either for disposal or for continued storage. A number of materials are currently stored at AWE which either contain tritium or have been used in tritium processing. It is essential that these materials are characterised such that a strategy may be developed for their safe stewardship, and ultimately for their treatment and disposal. Treatment processes for such materials are determined by the application of best practicable means (BPM) studies in accordance with the requirements of the Environment Agency of England and Wales. Clearly, it is necessary to understand the objectives of legacy material treatment / processing and the technical options available before a definitive BPM study is implemented. The majority of tritium legacy materials with which we are concerned originate from the decommissioning of a facility that was operational from the late 1950's through to the late 1990's when, on post-operative clear-out (POCO), the entire removable and transportable tritium inventory was moved to new, purpose built facilities. One of the principle tasks to be undertaken in the new facilities is the treatment of the legacy materials to recover tritium wherever practicable, and render the residual materials passively safe for disposal or continued storage. Where tritium recovery was not reasonably or technically feasible, then a means to assure continued safe storage was to be devised and implemented. The legacy materials are in the following forms: - Uranium beds which may or may not contain adsorbed tritium gas; - Tritium gas stored in containers; - Tritide targets for neutron generation; - Tritides of a broad spectrum of metals manufactured for research / long

  15. The Tritium White Paper

    International Nuclear Information System (INIS)

    2009-01-01

    This publication proposes a synthesis of the activities of two work-groups between May 2008 and April 2010. It reports the ASN's (the French Agency for Nuclear Safety) point of view, describes its activities and actions, and gives some recommendations. It gives a large and detailed overview of the knowledge status on tritium: tritium source inventory, tritium origin, management processes, capture techniques, reduction, tritium metrology, impact on the environment, impacts on human beings

  16. Dissolved atmospheric gas in xylem sap measured with membrane inlet mass spectrometry.

    Science.gov (United States)

    Schenk, H Jochen; Espino, Susana; Visser, Ate; Esser, Bradley K

    2016-04-01

    A new method is described for measuring dissolved gas concentrations in small volumes of xylem sap using membrane inlet mass spectrometry. The technique can be used to determine concentrations of atmospheric gases, such as argon, as reported here, or for any dissolved gases and their isotopes for a variety of applications, such as rapid detection of trace gases from groundwater only hours after they were taken up by trees and rooting depth estimation. Atmospheric gas content in xylem sap directly affects the conditions and mechanisms that allow for gas removal from xylem embolisms, because gas can dissolve into saturated or supersaturated sap only under gas pressure that is above atmospheric pressure. The method was tested for red trumpet vine, Distictis buccinatoria (Bignoniaceae), by measuring atmospheric gas concentrations in sap collected at times of minimum and maximum daily temperature and during temperature increase and decline. Mean argon concentration in xylem sap did not differ significantly from saturation levels for the temperature and pressure conditions at any time of collection, but more than 40% of all samples were supersaturated, especially during the warm parts of day. There was no significant diurnal pattern, due to high variability between samples. © 2015 John Wiley & Sons Ltd.

  17. Development of data logger for atmospheric pressure, temperature and relative humidity for gas-filled detector

    International Nuclear Information System (INIS)

    Sahu, S.; Sahu, P.K.; Bhuyan, M.R.; Biswas, S.; Mohanty, B.

    2014-01-01

    At IoP-NISER an initiative has been taken to build and test micro-pattern gas detector such as Gas Electron Multiplier (GEM) for several upcoming High-Energy Physics (HEP) experiment projects. Temperature (t), atmospheric pressure (p) and relative humidity (RH) monitor and recording is very important for gas filled detector development. A data logger to monitor and record the ambient parameters such as temperature, relative humidity and pressure has been developed. With this data logger continuous recording of t, p, RH and time stamp can be done with a programmable sampling interval. This data is necessary to correct the gain of a gas filled detector

  18. Tritium conductivity and isotope effect in proton-conducting perovskites

    International Nuclear Information System (INIS)

    Mukundan, R.; Brosha, E.L.; Birdsell, S.A.; Costello, A.L.; Garzon, F.H.; Willms, R.S.

    1999-01-01

    The tritium ion conductivities of SrZr 0.9 Yb 0.1 O 2.95 and BaCe 0.9 Yb 0.1 O 2.95 have been measured by ac impedance analysis. The high tritium conductivity of these perovskites could potentially lead to their application as an electrochemical membrane for the recovery of tritium from tritiated gas streams. The conductivities of these perovskites, along with SrCe 0.95 Yb 0.05 O 2.975 , were also measured in hydrogen- and deuterium-containing atmospheres to illustrate the isotope effect. For the strontium zirconate and barium cerate samples, the impedance plot consists of two clearly resolved arcs, a bulk and a grain boundary arc, in the temperature range 50--350 C. However, for the strontium cerate sample, the clear resolution of the bulk conductivity was not possible and only the total conductivity was measurable. Thus, the isotope effect was clearly established only for the strontium zirconate and barium cerate samples. The decrease in bulk conductivity with increasing isotope mass was found to be a result of an increase in the activation energy for conduction accompanied by a decrease in the pre-exponential factor. Since the concentration of the mobile species (H+, D+, or T+) should remain relatively constant at T < 350 C, this increase in activation energy is directly attributable to the increased activation energy for the isotope mobility

  19. Improving tritium exposure reconstructions using accelerator mass spectrometry

    International Nuclear Information System (INIS)

    Love, A.H.; Hunt, J.R.; Vogel, J.S.; Knezovich, J.P.

    2004-01-01

    Direct measurement of tritium atoms by accelerator mass spectrometry (AMS) enables rapid low-activity tritium measurements from milligram-sized samples and permits greater ease of sample collection, faster throughput, and increased spatial and/or temporal resolution. Because existing methodologies for quantifying tritium have some significant limitations, the development of tritium AMS has allowed improvements in reconstructing tritium exposure concentrations from environmental measurements and provides an important additional tool in assessing the temporal and spatial distribution of chronic exposure. Tritium exposure reconstructions using AMS were previously demonstrated for a tree growing on known levels of tritiated water and for trees exposed to atmospheric releases of tritiated water vapor. In these analyses, tritium levels were measured from milligram-sized samples with sample preparation times of a few days. Hundreds of samples were analyzed within a few months of sample collection and resulted in the reconstruction of spatial and temporal exposure from tritium releases. Although the current quantification limit of tritium AMS is not adequate to determine natural environmental variations in tritium concentrations, it is expected to be sufficient for studies assessing possible health effects from chronic environmental tritium exposure. (orig.)

  20. Improving tritium exposure reconstructions using accelerator mass spectrometry

    Science.gov (United States)

    Hunt, J. R.; Vogel, J. S.; Knezovich, J. P.

    2010-01-01

    Direct measurement of tritium atoms by accelerator mass spectrometry (AMS) enables rapid low-activity tritium measurements from milligram-sized samples and permits greater ease of sample collection, faster throughput, and increased spatial and/or temporal resolution. Because existing methodologies for quantifying tritium have some significant limitations, the development of tritium AMS has allowed improvements in reconstructing tritium exposure concentrations from environmental measurements and provides an important additional tool in assessing the temporal and spatial distribution of chronic exposure. Tritium exposure reconstructions using AMS were previously demonstrated for a tree growing on known levels of tritiated water and for trees exposed to atmospheric releases of tritiated water vapor. In these analyses, tritium levels were measured from milligram-sized samples with sample preparation times of a few days. Hundreds of samples were analyzed within a few months of sample collection and resulted in the reconstruction of spatial and temporal exposure from tritium releases. Although the current quantification limit of tritium AMS is not adequate to determine natural environmental variations in tritium concentrations, it is expected to be sufficient for studies assessing possible health effects from chronic environmental tritium exposure. PMID:14735274

  1. Safe handling of tritium

    International Nuclear Information System (INIS)

    1991-01-01

    The main objective of this publication is to provide practical guidance and recommendations on operational radiation protection aspects related to the safe handling of tritium in laboratories, industrial-scale nuclear facilities such as heavy-water reactors, tritium removal plants and fission fuel reprocessing plants, and facilities for manufacturing commercial tritium-containing devices and radiochemicals. The requirements of nuclear fusion reactors are not addressed specifically, since there is as yet no tritium handling experience with them. However, much of the material covered is expected to be relevant to them as well. Annex III briefly addresses problems in the comparatively small-scale use of tritium at universities, medical research centres and similar establishments. However, the main subject of this publication is the handling of larger quantities of tritium. Operational aspects include designing for tritium safety, safe handling practice, the selection of tritium-compatible materials and equipment, exposure assessment, monitoring, contamination control and the design and use of personal protective equipment. This publication does not address the technologies involved in tritium control and cleanup of effluents, tritium removal, or immobilization and disposal of tritium wastes, nor does it address the environmental behaviour of tritium. Refs, figs and tabs

  2. Apparent enrichment of organically bound tritium in rivers explained by the heritage of our past.

    Science.gov (United States)

    Eyrolle-Boyer, Frédérique; Boyer, Patrick; Claval, David; Charmasson, Sabine; Cossonnet, Catherine

    2014-10-01

    The global inventory of naturally produced tritium (3H) is estimated at 2.65 kg, whereas more than 600 kg have been released during atmospheric nuclear tests (NCRP, 1979; UNSCEAR, 2000) constituting the main source of artificial tritium throughout the Anthropocene. The behaviour of this radioactive isotope in the environment has been widely studied since the 1950s, both through laboratory experiments and, more recently, through field observations (e.g., Cline, 1953; Kirchmann et al., 1979; Daillant et al., 2004; McCubbin et al., 2001; Kim et al., 2012). In its "free" forms, [i.e. 3H gas or 3H hydride (HT); methyl 3H gas (CH3T); tritiated H2O or 3H-oxide (HTO); and Tissue Free Water 3H (TFWT)], tritium closely follows the water cycle. However, 3H bound with organic compounds, mainly during the basic stages of photosynthesis or through weak hydrogen links, is less exchangeable with water, which explains its persistence in the carbon cycle as re underlined recently by Baglan et al. (2013), Jean-Batiste and Fourré (2013), Kim et al. (2013a,b). In this paper, we demonstrate that terrestrial biomass pools, historically contaminated by global atmospheric fallout from nuclear testing, have constituted a significant delayed source of organically bound tritium (OBT) for aquatic systems, resulting in an apparent enrichment of OBT as compared to HTO. This finding helps to explain concentration factors (tritium concentration in biota/concentration in water) greater than 1 observed in areas that are not directly affected by industrial radioactive wastes, and thus sheds light on the controversies regarding tritium 'bioaccumulation'. Such apparent enrichment of OBT is expected to be more pronounced in the Northern Hemisphere where fallout was most significant, depending on the nature and biodegradability of terrestrial biomass at the regional scale. We further believe that OBT transfers from the continent to oceans have been sufficient to affect tritium concentrations in

  3. Experimental investigation of gas heating and dissociation in a microwave plasma torch at atmospheric pressure

    International Nuclear Information System (INIS)

    Su, Liu; Kumar, Rajneesh; Ogungbesan, Babajide; Sassi, Mohamed

    2014-01-01

    Highlights: • Atmospheric-pressure microwave plasma torch. • Gas heating and dissociation. • Parametric studies of plasma operating conditions. • Local thermal equilibrium plasma. - Abstract: Experimental investigations are made to understand gas heating and dissociation in a microwave (MW) plasma torch at atmospheric pressure. The MW induced plasma torch operates at 2.45 GHz frequency and up to 2 kW power. Three different gas mixtures are injected in the form of axial flow and swirl flow in a quartz tube plasma torch to experimentally investigate the MW plasma to gas energy transfer. Air–argon, air–air and air–nitrogen plasmas are formed and their operational ranges are determined in terms of gas flow rates and MW power. Visual observations, optical emission spectroscopy and K-type thermocouple measurements are used to characterize the plasma. The study reveals that the plasma structure is highly dependent on the carrier gas type, gas flow rate, and MW power. However, the plasma gas temperature is shown not to vary much with these parameters. Further spectral and analytical analysis show that the plasma is in thermal equilibrium and presents very good energy coupling between the microwave power and gas heating and dissociation. The MW plasma torch outlet temperature is also measured and found to be suitable for many thermal heating and chemical dissociation applications

  4. BEATRIX-II: In-situ tritium recovery data correction

    International Nuclear Information System (INIS)

    Slagle, O.D.; Hollenberg, G.W.; Kurasawa, T.; Verrall, R.A.

    1993-09-01

    BEATRIX-II was an in-situ tritium recovery experiment in a fast reactor to characterize the irradiation behavior of fusion ceramic breeder materials. Correcting and compiling the in-situ tritium recovery data involved correcting the ion chamber response for the effect of sweep gas composition or amount of hydrogen in the helium sweep gas and for the buildup of background. The effect of sweep gas composition was addressed in the previous workshop. During the operation of Phase I of the experiment the backgrounds of the ion chambers were found to reach significant levels relative to the tritium recovery concentrations in the sweep gas from the specimen canisters. The measured tritium concentrations were corrected for background by comparing the tritium recovery rate during reference conditions with the predicted tritium generation rate. Background increases were found to be associated with tritium recovery peaks and elevated levels of moisture in the sweep gas. These conditions typically occurred when the hydrogen concentration in the sweep gas was increased to 0.1% after extended operation in He or He-0.01% H 2 . Three examples of this increase in ionization chamber background are described. The final corrected BEATRIX-II, Phase I tritium recovery data provide a valuable resource to be used for predicting the performance of Li 2 O in a fusion blanket application

  5. Tritium retention and clean-up in JET

    International Nuclear Information System (INIS)

    Andrew, P.; Brennan, P.D.; Coad, J.P.

    1999-01-01

    During 1997 JET operation with D-T plasmas, 35 g of tritium were introduced into the torus, mainly by gas puffing. It was found that during this period, the torus tritium inventory would accumulate at a rate of about 40% of the input. After tritium operation ceased, the experimental program continued with deuterium- and hydrogen-fuelled experiments, during which time the tritium inventory decreased to about 17% of the total input. Techniques aimed at detritiation of the torus included methods using deuterium gas (such as deuterium pulsing) which were used in the middle of the experimental campaign, and methods which could adversely affect the torus vacuum conditions (such as air purges) which were reserved for the period after the experimental campaign. Whilst it was found that the plasma tritium fraction could be reduced to below the 1% level in a few days, the tritium inventory reached a virtually steady level of about 6 g by the end of the campaign. (orig.)

  6. Tritium monitoring in environment at ICIT Tritium Separation Facility

    International Nuclear Information System (INIS)

    Varlam, Carmen; Stefanescu, I.; Vagner, Irina; Faurescu, I.; Toma, A.; Dulama, C.; Dobrin, R.

    2008-01-01

    Full text: The Cryogenic Pilot is an experimental project developed within the national nuclear energy research program, which is designed to develop the required technologies for tritium and deuterium separation by cryogenic distillation of heavy water. The process used in this installation is based on a combination between liquid-phase catalytic exchange (LPCE) and cryogenic distillation. Basically, there are two ways that the Cryogenic Pilot could interact with the environment: by direct atmospheric release and through the sewage system. This experimental installation is located 15 km near the region biggest city and in the vicinity - about 1 km, of Olt River. It must be specified that in the investigated area there is an increased chemical activity; almost the entire Experimental Cryogenic Pilot's neighborhood is full of active chemical installations. This aspect is really essential for our study because the sewerage system is connected with the other three chemical plants from the neighborhood. For that reason we progressively established elements of an environmental monitoring program well in advance of tritium operation in order to determine baseline levels. The first step was the tritium level monitoring in environmental water and wastewater of industrial activity from neighborhood. In order to establish the base level of tritium concentration in the environment around the nuclear facilities, we investigated the sample preparation treatment for different types of samples: onion, green beams, grass, apple, garden lettuce, tomato, cabbage, strawberry and grapes. We used azeotropic distillation of all types of samples, the carrier solvent being toluene from different Romanian providers. All measurements for the determination of environmental tritium concentration were performed using liquid scintillation counting (LSC), with the Quantulus 1220 spectrometer. (authors)

  7. Generation of gaseous tritium standards

    International Nuclear Information System (INIS)

    Hohorst, F.A.

    1994-09-01

    The determination of aqueous and non-aqueous tritium in gaseous samples is one type of determination often requested of radioanalytical laboratories. This determination can be made by introducing the sample as a gas into a sampling train containing two silica gel beds separated by.a catalytic oxidizer bed. The first bed traps tritiated water. The sample then passes into and through the oxidizer bed where non-aqueous tritium containing species are oxidized to water and other products of combustion. The second silica gel bed then traps the newly formed tritiated water. Subsequently, silica gel is removed to plastic bottles, deionized water is added, and the mixture is permitted to equilibrate. The tritium content of the equilibrium mixture is then determined by conventional liquid scintillation counting (LSC). For many years, the moisture content of inert, gaseous samples has been determined using monitors which quantitatively electrolyze the moisture present after that moisture has been absorbed by phosphorous pentoxide or other absorbents. The electrochemical reaction is quantitative and definitive, and the energy consumed during electrolysis forms the basis of the continuous display of the moisture present. This report discusses the experimental evaluation of such a monitor as the basis for a technique for conversion of small quantities of SRMs of tritiated water ( 3 HOH) into gaseous tritium standards ( 3 HH)

  8. Two investigations concerning the release of tritium. I. Tritium leakage from 3H(Sc) EC-detectors

    International Nuclear Information System (INIS)

    Bergman, C.; Wesslen, E.

    1977-01-01

    Recently the manufacturers of EC-detectors for gas chromatographs introduced a new type of 3 H EC-detector where the tritium is bound to scandium instead of to titanium and has an activity up to 1 Ci. It is expected that the scandium-based detector will take a great part of the Swedish EC-detector market. The Swedish National Institute of Radiation Protection is anxious to make sure that the introduction of the new detector, which will be used at higher temperature, will not give rise to any increased risk of tritium intake to the personnel handling the chromatographs. The leakage of tritium from commercially available 3 H(Sc) EC-detectors containing 1 Ci of tritium was measured as a function of the detector temperature. Tritium appears both in the form of tritium gas dissolved in the scandium and in the form of tritide. The gas evaporates rather easily with increasing temperature while the dissociation of the tritide is a slower process. The evaporation of tritium due to the dissociation of the tritide was found to be negligible, less than 0.2 μCi/h at temperatures less than 100 0 C, but rises rapidly with temperature. The study also showed that even when the detector is stored at room temperature, a re-distribution of the tritium occures, from the tritide to the dissolved tritium gas, which then easily evaporates even at moderately elevated temperatures

  9. Procedures for the retention of gaseous tritium released from a tritium enrichment plant

    International Nuclear Information System (INIS)

    Gutowski, H.; Bracha, M.

    1987-01-01

    General aim of the study is the comparison of two alternative processes for the retention of gaseous tritium which is released during normal operation and emergency operation in a tritium-enrichment-plant. Two processes for the retention of tritium were compared: 1. Oxidation-process. The hydrogen-gas containing HT will be burnt on an oxidation catalyst to H 2 O and HTO. In a subsequent step the water will be removed from the process by condensation, freezing and adsorption. 2. TROC-process (Tritium Removal by Organic Compounds). The tritium is added to an organic compound (acid) via catalyst. This reaction is irreversible and leads to solid products. (orig./RB) [de

  10. Application of the permeation to the production of low radioactive calibrated gas flows. Low radioactive tritium measurement

    International Nuclear Information System (INIS)

    Pilot, Guy.

    1979-12-01

    The permeation of compounds (HT, HTO, 131 ICH 3 , and 129 ICH 3 ) through organic membranes in view of producing low radioactive calibrated gas flows has been studied. This process of which the diffusion is the main stage enables respecting certain conditions (choice of the membrane, temperature, partial pressure differential) our aims to be reached with a good accuracy. In order to measure radioactivity of tritiated standard gases, a detector was built. This detector is an Oeschger type proportional counter with a total volume of 17.4 dm 3 and an useful volume of 3.9 dm 3 . In the conditions of operation, the background is of 1.7.10 -6 I s -1 cm -3 . The counter coupled with a feed-rack enables various samples to be measured and it is possible in the best conditions to detect some 10 -11 μCi cm -3 NTP [fr

  11. Tritium Room Air Monitor Operating Experience Review

    Energy Technology Data Exchange (ETDEWEB)

    L. C. Cadwallader; B. J. Denny

    2008-09-01

    Monitoring the breathing air in tritium facility rooms for airborne tritium is a radiological safety requirement and a best practice for personnel safety. Besides audible alarms for room evacuation, these monitors often send signals for process shutdown, ventilation isolation, and cleanup system actuation to mitigate releases and prevent tritium spread to the environment. Therefore, these monitors are important not only to personnel safety but also to public safety and environmental protection. This paper presents an operating experience review of tritium monitor performance on demand during small (1 mCi to 1 Ci) operational releases, and intentional airborne inroom tritium release tests. The tritium tests provide monitor operation data to allow calculation of a statistical estimate for the reliability of monitors annunciating in actual tritium gas airborne release situations. The data show a failure to operate rate of 3.5E-06/monitor-hr with an upper bound of 4.7E-06, a failure to alarm on demand rate of 1.4E-02/demand with an upper bound of 4.4E-02, and a spurious alarm rate of 0.1 to 0.2/monitor-yr.

  12. Microseepage of methane to the atmosphere from the Dawanqi oil-gas field, Tarim Basin, China

    Science.gov (United States)

    Tang, Junhong; Xu, Yue; Wang, Guojian; Etiope, Giuseppe; Han, Wei; Yao, Zhitong; Huang, Jingang

    2017-04-01

    The microseepage of natural gas from subsurface hydrocarbon reservoirs is a widespread process in petroleum basins. On a global scale, microseepage represents an important natural source of atmospheric methane (CH4). To date, microseepage CH4 flux data have been obtained from 20 petroleum systems in North America, Europe, and Asia. While the seasonal variations of gas flux due to soil methanotrophic activity are known, the role of geological factors in controlling gas fluxes has been poorly investigated. Here we present new microseepage data from the Dawanqi oil-gas field located within the Tarim Basin (China), a petroleum system characterized by intense faulting and shallow (petroleum fields with active tectonics. Our results confirm that dry soil over petroleum fields can be a net source of atmospheric CH4 and its flux is primarily controlled by faulting, and reservoir depth and pressure. These factors shall be considered in global bottom-up seepage emission estimates.

  13. Radon gas-exchange rate through the interface sea atmosphere in the coast

    International Nuclear Information System (INIS)

    Duenas, C.; Fernandez, M.C.; Perez Martinez, M.

    1985-01-01

    The Rn gas exchange velocity through the interface sea atmosphere has been estimated. Our measurements have been made in a sampler station located in Malaga bay, obtaining a mean value of 0.45 m/d. The corresponding magnitude of the thickness of boundary layer is 316μ. Experimental results are discussed. No clear relationship can be found between the gas exchange rate and wind speed. (author)

  14. Environmental aspects of tritium

    International Nuclear Information System (INIS)

    Quisenberry, D.R.

    1979-01-01

    The potential radiological implications of environmental tritium releases must be determined in order to develop a programme for dealing with the tritium inventory predicted for the nuclear power industry which, though still in its infancy, produces tritium in megacurie quantities annually. Should the development of fusion power generation become a reality, it will create a potential source for large releases of tritium, much of it in the gaseous state. At present about 90% of the tritium produced enters the environment through gaseous and liquid effluents and is deposited in the hydrosphere as tritiated water. Tritium can be assimilated by plants and animals and organically bound, regardless of the exposure pathway. However, there appears to be no concentration factor relative to hydrogen at any level of food chains analysed to date. The body burden, for man, is dependent on the exposure pathway and tissue-bound fractions are primarily the result of organically bound tritium in food. (author)

  15. HARAD, Decay Isotope Concentration from Atmospheric Noble-Gas Release

    International Nuclear Information System (INIS)

    Moore, R.E.

    1986-01-01

    1 - Description of problem or function: HARAD calculates concentrations of radioactive daughters in air following the atmospheric release of a parent radionuclide for a variety of release heights and meteorological conditions. It can be applied most profitably to the assessment of doses to man from the noble gases such as Rn-222, Rn-220, and Xe and Kr isotopes. These gases can produce significant quantities of short-lived particulate daughters in an airborne plume, which are the major contributors to dose. The simultaneous processes of radioactive decay, buildup and environmental loss due to wet and dry deposition on ground surfaces are calculated for a daughter chain in an airborne plume as it is dispersed downwind from a point of release of a parent. 2 - Method of solution: The code evaluates the analytic solution to the set of coupled first order differential equations describing time variation of the concentration of a chain of radionuclides. The analytic solutions assume that the coefficient describing the fractional rate of dry deposition is constant with time. To account for the variation the time coordinate is automatically divided into intervals and a set of average values are used. 3 - Restrictions on the complexity of the problem: - The maximum length of decay chain is 10 nuclides; calculations can be made at a maximum of 24 downwind distances

  16. Influence of Gas Atmosphere Dew Point on the Galvannealing of CMnSi TRIP Steel

    Science.gov (United States)

    Cho, Lawrence; Kim, Myung Soo; Kim, Young Ha; De Cooman, Bruno C.

    2013-11-01

    The Fe-Zn reaction occurring during the galvannealing of a Si-bearing transformation-induced plasticity (TRIP) steel was investigated by field-emission electron probe microanalysis and field-emission transmission electron microscopy. The galvannealing was simulated after hot dipping in a Zn bath containing 0.13 mass pct Al at 733 K (460 °C). The galvannealing temperature was in the range of 813 K to 843 K (540 °C to 570 °C). The kinetics and mechanism of the galvannealing reaction were strongly influenced by the gas atmosphere dew point (DP). After the galvannealing of a panel annealed in a N2+10 pct H2 gas atmosphere with low DPs [213 K and 243 K (-60 °C and -30 °C)], the coating layer consisted of δ (FeZn10) and η (Zn) phase crystals. The Mn-Si compound oxides formed during intercritical annealing were present mostly at the steel/coating interface after the galvannealing. Galvannealing of a panel annealed in higher DP [263 K and 273 K, and 278 K (-10 °C, 0 °C, and +5 °C)] gas atmospheres resulted in a coating layer consisting of δ and Г (Fe3Zn10) phase crystals, and a thin layer of Г 1 (Fe11Zn40) phase crystals at the steel/coating interface. The Mn-Si oxides were distributed homogeneously throughout the galvannealed (GA) coating layer. When the surface oxide layer thickness on panels annealed in a high DP gas atmosphere was reduced, the Fe content at the GA coating surface increased. Annealing in a higher DP gas atmosphere improved the coating quality of the GA panels because a thinner layer of oxides was formed. A high DP atmosphere can therefore significantly contribute to the suppression of Zn-alloy coating defects on CMnSi TRIP steel processed in hot dip galvanizing lines.

  17. Tritium release from lithium titanate, a low-activation tritium breeding material

    International Nuclear Information System (INIS)

    Kopasz, J.P.; Miller, J.M.; Johnson, C.E.

    1994-01-01

    The goals for fusion power are to produce energy in as safe, economical, and environmentally benign a manner as possible. To ensure environmentally sound operation low-activation materials should be used where feasible. The ARIES Tokamak Reactor Study has based reactor designs on the concept of using low-activation materials throughout the fusion reactor. For the tritium breeding blanket, the choices for low activation tritium breeding materials are limited. Lithium titanate is an alternative low-activation ceramic material for use in the tritium breeding blanket. To date, very little work has been done on characterizing the tritium release for lithium titanate. We have thus performed laboratory studies of tritium release from irradiated lithium titanate. The results indicate that tritium is easily removed from lithium titanate at temperatures as low as 600 K. The method of titanate preparation was found to affect the tritium release, and the addition of 0.1% H 2 to the helium purge gas did not improve tritium recovery. ((orig.))

  18. Tritium in the environment. The IRSN's opinion on key issues and on research and development perspectives

    International Nuclear Information System (INIS)

    2010-01-01

    This report states the opinion of the IRSN on issues related to the behaviour of tritium in the environment, and to the associated risks. This report is based on a set of studies and researches performed on this radionuclide. Thus, the authors address the status of knowledge on the evolution of tritium released by nuclear activities (measurement techniques), the risk of bioaccumulation of tritium by living organisms within ecosystems (behaviour of tritium in the atmosphere, in soils, in ground plants, in continental and sea aquatic media), and the knowledge of risks due to tritium absorbed by living organisms (dose assessment, knowledge of tritium harmful effects and relative biological effectiveness)

  19. Simulation of the impact of thunderstorm activity on atmospheric gas composition

    Science.gov (United States)

    Smyshlyaev, S. P.; Mareev, E. A.; Galin, V. Ya.

    2010-08-01

    A chemistry-climate model of the lower and middle atmosphere has been used to estimate the sensitivity of the atmospheric gas composition to the rate of thunderstorm production of nitrogen oxides at upper tropospheric and lower stratospheric altitudes. The impact that nitrogen oxides produced by lightning have on the atmospheric gas composition is treated as a subgrid-scale process and included in the model parametrically. The natural uncertainty in the global production rate of nitrogen oxides in lightning flashes was specified within limits from 2 to 20 Tg N/year. Results of the model experiments have shown that, due to the variability of thunderstorm-produced nitrogen oxides, their concentration in the upper troposphere and lower stratosphere can vary by a factor of 2 or 3, which, given the influence of nitrogen oxides on ozone and other gases, creates the potential for a strong perturbation of the atmospheric gas composition and thermal regime. Model calculations have shown the strong sensitivity of ozone and the OH hydroxyl to the amount of lightning nitrogen oxides at different atmospheric altitudes. These calculations demonstrate the importance of nitrogen oxides of thunderstorm origin for the balance of atmospheric odd ozone and gases linked to it, such as ozone and hydroxyl radicals. Our results demonstrate that one important task is to raise the accuracy of estimates of the rate of nitrogen oxide production by lightning discharges and to use physical parametrizations that take into account the local lightning effects and feedbacks arising in this case rather than climatological data in models of the gas composition and general circulation of the atmosphere.

  20. Helium effects on tritium storage materials

    International Nuclear Information System (INIS)

    Moysan, I.; Contreras, S.; Demoment, J.

    2008-01-01

    For ten years French Tritium laboratories have been using metal hydride storage beds with LaNi 4 Mn for process gas (HDT mixture) absorption, desorption and for both short and long term storage. This material has been chosen because of its low equilibrium pressure and of its ability to retain decay helium 3 in its lattice. Aging effects on the thermodynamic behavior of LaNi 4 Mn have been investigated. Aging, due to formation of helium 3 in the lattice, decreases the desorption isotherm plateau pressure and shifts the α phase to the higher stoichiometries. Life time of the two kinds of tritium (and isotopes) storage vessels managed in the laboratory depends on these aging changes. The Tritium Long Term Storage (namely STLT) and the hydride storage vessel (namely FSH 400) are based on LaNi 4 Mn even though they are not used for the same applications. STLT contains LaNi 4 Mn in an aluminum vessel and is designed for long term pure tritium storage. The FSH 400 is composed of LaNi 4 Mn included within a stainless steel container. This design is aimed at storing low tritium content mixtures (less than 3% of tritium) and for supplying processes with HDT gas. Life time of the STLT can reach 12 years. Life time of the FSH 400 varies from 1.2 years to more than 25 years depending on the application. (authors)

  1. Helium effects on tritium storage materials

    Energy Technology Data Exchange (ETDEWEB)

    Moysan, I.; Contreras, S.; Demoment, J. [CEA Valduc, Service HDT, 21 - Is-sur-Tille (France)

    2008-07-15

    For ten years French Tritium laboratories have been using metal hydride storage beds with LaNi{sub 4}Mn for process gas (HDT mixture) absorption, desorption and for both short and long term storage. This material has been chosen because of its low equilibrium pressure and of its ability to retain decay helium 3 in its lattice. Aging effects on the thermodynamic behavior of LaNi{sub 4}Mn have been investigated. Aging, due to formation of helium 3 in the lattice, decreases the desorption isotherm plateau pressure and shifts the {alpha} phase to the higher stoichiometries. Life time of the two kinds of tritium (and isotopes) storage vessels managed in the laboratory depends on these aging changes. The Tritium Long Term Storage (namely STLT) and the hydride storage vessel (namely FSH 400) are based on LaNi{sub 4}Mn even though they are not used for the same applications. STLT contains LaNi{sub 4}Mn in an aluminum vessel and is designed for long term pure tritium storage. The FSH 400 is composed of LaNi{sub 4}Mn included within a stainless steel container. This design is aimed at storing low tritium content mixtures (less than 3% of tritium) and for supplying processes with HDT gas. Life time of the STLT can reach 12 years. Life time of the FSH 400 varies from 1.2 years to more than 25 years depending on the application. (authors)

  2. Development of tritium-handling technique

    International Nuclear Information System (INIS)

    Ohmura, Hiroshi; Hosaka, Akio; Okamoto, Takahumi

    1988-01-01

    The overview of developing activities for tritium-handling techniques in IHI are presented. To establish a fusion power plant, tritium handling is one of the key technologies. Recently in JAERI, conceptual design of FER (Fusion Experimental Reactor) has been carried out, and the FER system requires a processing system for a large amount of tritium. IHI concentrate on investigation of fuel gas purification, isotope separation and storage systems under contract with Toshiba Corporation. Design results of the systems and each components are reviewed. IHI has been developing fundamental handling techniques which are the ZrNi bed for hydrogen isotope storage and isotope separation by laser. The ZrNi bed with a tritium storage capacity of 1000 Ci has been constructed and recovery capability of the hydrogen isotope until 10 -4 Torr {0.013 Pa} was confirmed. In laser isotope separation, the optimum laser wave length has been determined. (author)

  3. Initial experience of tritium exposure control at JET

    International Nuclear Information System (INIS)

    Patel, B.; Campling, D.C.; Schofield, P.A.; Macheta, P.; Sandland, K.

    1998-01-01

    Some of the safety procedures and controls in place for work with tritium are described, and initial operational experience of handling tritium is discussed. A description is given of work to rectify a water leak in a JET neutral beam heating component, which involved man-access to a confined volume to perform repairs, at tritium levels about 100 DAC (80 MBq/m 3 . HTO). Control measures involving use of purge and extract ventilation, and of personal protection using air-fed pressurized suits are described. Results are given of the internal doses to project staff and of atmospheric discharges of tritium during the repair outage. (P.A.)

  4. Overview of tritium systems for the Compact Ignition Tokamak

    International Nuclear Information System (INIS)

    Bartlit, J.R.; Gruetzmacher, K.M.; Fleming, R.B.

    1987-01-01

    The Compact Ignition Tokamak (CIT) is being designed at several laboratories to produce and study fully ignited plasma discharges. The tritium systems which will be needed for CIT include fueling systems and radiation monitoring and safety systems. Design of the tritium systems is the responsibility of the Tritium Systems Test Assembly (TSTA) at Los Alamos National Laboratory. Major new tritium systems for CIT include a pellet injector, an air detritiation system and a glovebox atmosphere detritiation system. The pellet injector is being developed at Oak Ridge National Laboratory. 7 refs., 2 figs

  5. Tritium release during inspection of reactor 'RA' at 'Vinca' institute

    International Nuclear Information System (INIS)

    Sipka, V.; Miljevic, N.; Grsic, Z.; Todorovic, D.; Radenkovic, M.

    1997-01-01

    Tritium content in daily precipitation, atmospheric water vapor inside of the reactor hall and around 'Vinca' Institute as well as in soil up to 800 m distance was monitoring during the regular inspection of the fuel channels. Tritium activity in the reactor hall air moisture was in the range from 0.022 to 6.7 MBq/m 3 . Tritium content in soil moisture between 12.7 and 530.9 Bq/l indicate a certain contamination due to tritium release in the environment, depending on the depth and distance from the place of release (author) [sr

  6. An approach for verifying biogenic greenhouse gas emissions inventories with atmospheric CO2 concentration data

    Science.gov (United States)

    Stephen M Ogle; Kenneth Davis; Thomas Lauvaux; Andrew Schuh; Dan Cooley; Tristram O West; Linda S Heath; Natasha L Miles; Scott Richardson; F Jay Breidt; James E Smith; Jessica L McCarty; Kevin R Gurney; Pieter Tans; A Scott. Denning

    2015-01-01

    Verifying national greenhouse gas (GHG) emissions inventories is a critical step to ensure that reported emissions data to the United Nations Framework Convention on Climate Change (UNFCCC) are accurate and representative of a country's contribution to GHG concentrations in the atmosphere. Furthermore, verifying biogenic fluxes provides a check on estimated...

  7. ObsPack: a framework for the preparation, delivery, and attribution of atmospheric greenhouse gas data

    NARCIS (Netherlands)

    Masarie, K. A.; Peters, W.; Jacobson, A. R.; Tans, P. P.

    2014-01-01

    Observation Package (ObsPack) is a framework designed to bring together atmospheric greenhouse gas observations from a variety of sampling platforms, prepare them with specific applications in mind, and package and distribute them in a self-consistent and well-documented product. Data products

  8. ObsPack: a framework for the preparation, delivery, and attribution of atmospheric greenhouse gas measurements

    NARCIS (Netherlands)

    Masarie, K. A.; Peters, W.; Jacobson, A. R.; Tans, P. P.

    2014-01-01

    Observation Package (ObsPack) is a framework designed to bring together atmospheric greenhouse gas observations from a variety of sampling platforms, prepare them with specific applications in mind, and package and distribute them in a self-consistent and well-documented product. Data products

  9. Atmospheric dispersion simulations of volcanic gas from Miyake Island by SPEEDI

    International Nuclear Information System (INIS)

    Nagai, Haruyasu; Furuno, Akiko; Terada, Hiroaki; Umeyama, Nobuaki; Yamazawa, Hiromi; Chino, Masamichi

    2001-03-01

    Japan Atomic Energy Research Institute is advancing the study for prediction of material circulation in the environment to cope with environmental pollution, based on SPEEDI (System for Prediction of Environmental Emergency Dose Information) and WSPEEDI (Worldwide version of SPEEDI), which are originally developed aiming at real-time prediction of atmospheric dispersion of radioactive substances accidentally released from nuclear facility. As a part of this study, dispersion simulation of volcanic gas erupted from Miyake Island is put into practice. After the stench incident at the west Kanto District on 28 August 2000 caused by volcanic gas from Miyake Island, the following simulations dealing with atmospheric dispersion of volcanic gas from Miyake Island have been carried out. (1) Retrospective simulation to analyze examine the mechanism of the transport of high concentration volcanic gas to the west Kanto District on 28 August and to estimate the release amount of volcanic gas. (2) Retrospective simulation to analyze the mechanism of the transport of volcanic gas to Tokai and Kansai districts in a case of stench incident on 13 September. (3) Automated real-time simulation from the acquisition of meteorological data to the output of figures for operational prediction of the transport of volcanic gas to Tokai and Kanto districts. This report describes the details of these studies. (author)

  10. Organically bound tritium

    International Nuclear Information System (INIS)

    Diabate, S.; Strack, S.

    1993-01-01

    Tritium released into the environment may be incorporated into organic matter. Organically bound tritium in that case will show retention times in organisms that are considerably longer than those of tritiated water which has significant consequences on dose estimates. This article reviews the most important processes of organically bound tritium production and transport through food networks. Metabolic reactions in plant and animal organisms with tritiated water as a reaction partner are of great importance in this respect. The most important production process, in quantitative terms, is photosynthesis in green plants. The translocation of organically bound tritium from the leaves to edible parts of crop plants should be considered in models of organically bound tritium behavior. Organically bound tritium enters the human body on several pathways, either from the primary producers (vegetable food) or at a higher tropic level (animal food). Animal experiments have shown that the dose due to ingestion of organically bound tritium can be up to twice as high as a comparable intake of tritiated water in gaseous or liquid form. In the environment, organically bound tritium in plants and animals is often found to have higher specific tritium concentrations than tissue water. This is not due to some tritium enrichment effects but to the fact that no equilibrium conditions are reached under natural conditions. 66 refs

  11. ABOUT THE POSSIBLE ROLE OF HYDROCARBON LAKES IN THE ORIGIN OF TITAN'S NOBLE GAS ATMOSPHERIC DEPLETION

    International Nuclear Information System (INIS)

    Cordier, D.; Mousis, O.; Lunine, J. I.; Lebonnois, S.; Lavvas, P.; Lobo, L. Q.; Ferreira, A. G. M.

    2010-01-01

    An unexpected feature of Titan's atmosphere is the strong depletion in primordial noble gases revealed by the Gas Chromatograph Mass Spectrometer aboard the Huygens probe during its descent on 2005 January 14. Although several plausible explanations have already been formulated, no definitive response to this issue has yet been found. Here, we investigate the possible sequestration of these noble gases in the liquid contained in lakes and wet terrains on Titan and the consequences for their atmospheric abundances. Considering the atmosphere and the liquid existing on the soil as a whole system, we compute the abundance of each noble gas relative to nitrogen. To do so, we make the assumption of thermodynamic equilibrium between the liquid and the atmosphere, the abundances of the different constituents being determined via regular solution theory. We find that xenon's atmospheric depletion can be explained by its dissolution at ambient temperature in the liquid presumably present on Titan's soil. In the cases of argon and krypton, we find that the fractions incorporated in the liquid are negligible, implying that an alternative mechanism must be invoked to explain their atmospheric depletion.

  12. Tritium systems test assembly stabilization

    International Nuclear Information System (INIS)

    Jasen, William G.; Michelotti, Roy A.; Anast, Kurt R.; Tesch, Charles

    2004-01-01

    The Tritium Systems Test Assembly (TSTA) was a facility dedicated to tritium technology Research and Development (R and D) primarily for future fusion power reactors. The facility was conceived in mid 1970's, operations commenced in early 1980's, stabilization and deactivation began in 2000 and were completed in 2003. The facility will remain in a Surveillance and Maintenance (S and M) mode until the Department of Energy (DOE) funds demolition of the facility, tentatively in 2009. A safe and stable end state was achieved by the TSTA Facility Stabilization Project (TFSP) in anticipation of long term S and M. At the start of the stabilization project, with an inventory of approximately 140 grams of tritium, the facility was designated a Hazard Category (HC) 2 Non-Reactor Nuclear facility as defined by US Department of Energy standard DOE-STD-1027-92 (1997). The TSTA facility comprises a laboratory area, supporting rooms, offices and associated laboratory space that included more than 20 major tritium handling systems. The project's focus was to reduce the tritium inventory by removing bulk tritium, tritiated water wastes, and tritium-contaminated high-inventory components. Any equipment that remained in the facility was stabilized in place. All of the gloveboxes and piping were rendered inoperative and vented to atmosphere. All equipment, and inventoried tritium contamination, remaining in the facility was left in a safe-and-stable state. The project used the End Points process as defined by the DOE Office of Environmental Management (web page http://www.em.doe.- gov/deact/epman.htmtlo) document and define the end state required for the stabilization of TSTA Facility. The End Points process added structure that was beneficial through virtually all phases of the project. At completion of the facility stabilization project the residual tritium inventory was approximately 3,000 curies, considerably less than the 1.6-gram threshold for a HC 3 facility. TSTA is now

  13. Experimental and Numerical Modelling of CO2 Atmospheric Dispersion in Hazardous Gas Emission Sites.

    Science.gov (United States)

    Gasparini, A.; sainz Gracia, A. S.; Grandia, F.; Bruno, J.

    2015-12-01

    Under stable atmospheric conditions and/or in presence of topographic depressions, CO2 concentrations can reach high values resulting in lethal effect to living organisms. The distribution of denser than air gases released from the underground is governed by gravity, turbulence and dispersion. Once emitted, the gas distribution is initially driven by buoyancy and a gas cloud accumulates on the ground (gravitational phase); with time the density gradient becomes less important due to dispersion or mixing and gas distribution is mainly governed by wind and atmospheric turbulence (passive dispersion phase). Natural analogues provide evidences of the impact of CO2 leakage. Dangerous CO2 concentration in atmosphere related to underground emission have been occasionally reported although the conditions favouring the persistence of such a concentration are barely studied.In this work, the dynamics of CO2 in the atmosphere after ground emission is assessed to quantify their potential risk. Two approaches have been followed: (1) direct measurement of air concentration in a natural emission site, where formation of a "CO2 lake" is common and (2) numerical atmospheric modelling. Two sites with different morphology were studied: (a) the Cañada Real site, a flat terrain in the Volcanic Field of Campo de Calatrava (Spain); (b) the Solforata di Pomezia site, a rough terrain in the Alban Hills Volcanic Region (Italy). The comparison between field data and model calculations reveal that numerical dispersion models are capable of predicting the formation of CO2 accumulation over the ground as a consequence of underground gas emission. Therefore, atmospheric modelling could be included as a valuable methodology in the risk assessment of leakage in natural degassing systems and in CCS projects. Conclusions from this work provide clues on whether leakage may be a real risk for humans and under which conditions this risk needs to be included in the risk assessment.

  14. Two dimensional radial gas flows in atmospheric pressure plasma-enhanced chemical vapor deposition

    Science.gov (United States)

    Kim, Gwihyun; Park, Seran; Shin, Hyunsu; Song, Seungho; Oh, Hoon-Jung; Ko, Dae Hong; Choi, Jung-Il; Baik, Seung Jae

    2017-12-01

    Atmospheric pressure (AP) operation of plasma-enhanced chemical vapor deposition (PECVD) is one of promising concepts for high quality and low cost processing. Atmospheric plasma discharge requires narrow gap configuration, which causes an inherent feature of AP PECVD. Two dimensional radial gas flows in AP PECVD induces radial variation of mass-transport and that of substrate temperature. The opposite trend of these variations would be the key consideration in the development of uniform deposition process. Another inherent feature of AP PECVD is confined plasma discharge, from which volume power density concept is derived as a key parameter for the control of deposition rate. We investigated deposition rate as a function of volume power density, gas flux, source gas partial pressure, hydrogen partial pressure, plasma source frequency, and substrate temperature; and derived a design guideline of deposition tool and process development in terms of deposition rate and uniformity.

  15. Evaluation of tritium release behavior from Li{sub 2}TiO{sub 3} during DT neutron irradiation by use of an improved tritium collection method

    Energy Technology Data Exchange (ETDEWEB)

    Edao, Yuki, E-mail: edao.yuki@jaea.go.jp [Tritium Technology Group, Department of Blanket Systems Research, Rokkasho Fusion Institute, Sector of Fusion Research and Development, Japan Atomic Energy Agency, 2-4 Shirane Shirakata, Tokai-mura, Naka-gun, Ibaraki 319-1195 (Japan); Kawamura, Yoshinori [Blanket Technology Group, Department of Blanket Systems Research, Rokkasho Fusion Institute, Sector of Fusion Research and Development, Japan Atomic Energy Agency, 801-1 Mukoyama, Naka, Ibaraki 311-0193 (Japan); Hoshino, Tsuyoshi [Breeding Functional Materials Development Group, Department of Blanket Systems Research, Rokkasho Fusion Institute, Sector of Fusion Research and Development, Japan Atomic Energy Agency, 2-166 Omotedate Obuchi, Rokkasho, Aomori 039-3212 (Japan); Ochiai, Kentaro [BA Project Coordination Group, Department of Fusion Power Systems Research, Rokkasho Fusion Institute, Sector of Fusion Research and Development, Japan Atomic Energy Agency, 2-166 Omotedate Obuchi, Rokkasho, Aomori 039-3212 (Japan)

    2016-11-15

    Highlights: • Behavior of tritium released from Li{sub 2}TiO{sub 3} under neutron irradiation was measured. • Tritium collection method with hydrophobic catalyst was demonstrated successfully. • Temperature of Li{sub 2}TiO{sub 3} was dominant to control the chemical form of tritium release. - Abstract: The accurate measurement of behavior of bred tritium released from a tritium breeder is indispensable to understand the behavior for a design of a tritium extraction system. The tritium collection method combined a CuO bed and water bubbles was not suitable to measure transient behavior of tritium released from Li{sub 2}TiO{sub 3} during neutron irradiation because tritium released behavior was changed to be delayed due to adsorption of oxidized tritium on the CuO. Hence, the tritium collection method with hydrophobic catalyst instead of the CuO was demonstrated and succeeded the accurate release measurement of tritium from Li{sub 2}TiO{sub 3}. With the method, we assessed the behavior of tritium release under the various conditions since tritium should be released from Li{sub 2}TiO{sub 3} as the form of HT as much as possible from the view point of the fuel cycle. Our results indicated; promotion of isotopic exchange reaction on the surface of Li{sub 2}TiO{sub 3} by addition of hydrogen in sweep gas is mandatory in order to release tritium smoothly from Li{sub 2}TiO{sub 3} irradiated with neutrons; the favorable sweep gas to release as the form of HT was hydrogen added inert gas; and the temperature of Li{sub 2}TiO{sub 3} was the dominant parameter to control the chemical form of tritium released from the Li{sub 2}TiO{sub 3}.

  16. A low tritium hydride bed inventory estimation technique

    Energy Technology Data Exchange (ETDEWEB)

    Klein, J.E.; Shanahan, K.L.; Baker, R.A. [Savannah River National Laboratory, Aiken, SC (United States); Foster, P.J. [Savannah River Nuclear Solutions, Aiken, SC (United States)

    2015-03-15

    Low tritium hydride beds were developed and deployed into tritium service in Savannah River Site. Process beds to be used for low concentration tritium gas were not fitted with instrumentation to perform the steady-state, flowing gas calorimetric inventory measurement method. Low tritium beds contain less than the detection limit of the IBA (In-Bed Accountability) technique used for tritium inventory. This paper describes two techniques for estimating tritium content and uncertainty for low tritium content beds to be used in the facility's physical inventory (PI). PI are performed periodically to assess the quantity of nuclear material used in a facility. The first approach (Mid-point approximation method - MPA) assumes the bed is half-full and uses a gas composition measurement to estimate the tritium inventory and uncertainty. The second approach utilizes the bed's hydride material pressure-composition-temperature (PCT) properties and a gas composition measurement to reduce the uncertainty in the calculated bed inventory.

  17. Reduction of weighing errors caused by tritium decay heating

    International Nuclear Information System (INIS)

    Shaw, J.F.

    1978-01-01

    The deuterium-tritium source gas mixture for laser targets is formulated by weight. Experiments show that the maximum weighing error caused by tritium decay heating is 0.2% for a 104-cm 3 mix vessel. Air cooling the vessel reduces the weighing error by 90%

  18. Technology and component development for a closed tritium cycle

    International Nuclear Information System (INIS)

    Penzhorn, R.D.; Haange, R.; Hircq, B.; Meikle, A.; Naruse, Y.

    1991-01-01

    A brief summary on recent advances in the field of tritium technology concerning the most important subsystems of the fuel cycle of a fusion reactor, i.e. the plasma exhaust pumping system, the exhaust gas clean up system, the isotope separation, the tritium storage and the tritium extraction from a blanket is provided. Experimental results, single component developments, and technical tests including those with relevant amounts of tritium that constitute the basis of proposed integral process concepts are described. 48 refs., 2 tabs

  19. Results of tritium tests performed on Sandia Laboratories decontamination system

    International Nuclear Information System (INIS)

    Gildea, P.D.; Wall, W.R.; Gede, V.P.

    1978-05-01

    The Tritium Research Laboratory (TRL), a facility for performing experiments using gram amounts of tritium, became operational on October 1, 1977. As secondary containment, the TRL employs sealed glove boxes connected on demand to two central decontamination systems, the Gas Purification System and the Vacuum Effluent Recovery System. Performance tests on these systems show the tritium removal systems can achieve concentration reduction factors (ratio of inlet to exhaust concentrations) much in excess of 1000 per pass at inlet concentrations of 1 part per million or less for both tritium and tritiated methane

  20. Discharge characteristics and hydrodynamics behaviors of atmospheric plasma jets produced in various gas flow patterns

    Science.gov (United States)

    Setsuhara, Yuichi; Uchida, Giichiro; Nakajima, Atsushi; Takenaka, Kosuke; Koga, Kazunori; Shiratani, Masaharu

    2015-09-01

    Atmospheric nonequilibrium plasma jets have been widely employed in biomedical applications. For biomedical applications, it is an important issue to understand the complicated mechanism of interaction of the plasma jet with liquid. In this study, we present analysis of the discharge characteristics of a plasma jet impinging onto the liquid surface under various gas flow patterns such as laminar and turbulence flows. For this purpose, we analyzed gas flow patters by using a Schlieren gas-flow imaging system in detail The plasma jet impinging into the liquid surface expands along the liquid surface. The diameter of the expanded plasma increases with gas flow rate, which is well explained by an increase in the diameter of the laminar gas-flow channel. When the gas flow rate is further increased, the gas flow mode transits from laminar to turbulence in the gas flow channel, which leads to the shortening of the plasm-jet length. Our experiment demonstrated that the gas flow patterns strongly affect the discharge characteristics in the plasma-jet system. This study was partly supported by a Grant-in-Aid for Scientific Research on Innovative Areas ``Plasma Medical Innovation'' (24108003) from the Ministry of Education, Culture, Sports, Science and Technology, Japan (MEXT).

  1. Contamination mechanisms of air basin with tritium in venues of underground nuclear explosions at the former Semipalatinsk test site.

    Science.gov (United States)

    Lyakhova, O N; Lukashenko, S N; Larionova, N V; Tur, Y S

    2012-11-01

    During the period of testing from 1945 to 1962 at the territory of Semipalatinsk test site (STS) within the Degelen Mountains in tunnels, 209 underground nuclear explosions were produced. Many of the tunnels have seasonal water seepage in the form of streams, through which tritium migrates from the underground nuclear explosion (UNE) venues towards the surface. The issue of tritium contamination occupies a special place in the radioactive contamination of the environment. In this paper we assess the level and distribution of tritium in the atmospheric air of ecosystems with water seepage at tunnels № 176 and № 177, located on "Degelen" site. There has been presented general nature of tritium distribution in the atmosphere relative to surface of a watercourse which has been contaminated with tritium. The basic mechanisms were studied for tritium distribution in the air of studied ecosystems, namely, the distribution of tritium in the systems: water-atmosphere, tunnel air-atmosphere, soil water-atmosphere, vegetation-atmosphere. An analytical calculation of tritium concentration in the atmosphere by the concentration of tritium in water has been performed. There has experimentally obtained the dependence for predictive assessment of tritium concentrations in air as a function of tritium concentration in one of the inlet sources such as water, tunnel air, soil water, vegetation, etc.. The paper also describes the general nature of tritium distribution in the air in the area "Degelen". Copyright © 2012 Elsevier Ltd. All rights reserved.

  2. The Effect of Thermal Convection on Earth-Atmosphere CO2 Gas Exchange in Aggregated Soil

    Science.gov (United States)

    Ganot, Y.; Weisbrod, N.; Dragila, M. I.

    2011-12-01

    Gas transport in soils and surface-atmosphere gas exchange are important processes that affect different aspects of soil science such as soil aeration, nutrient bio-availability, sorption kinetics, soil and groundwater pollution and soil remediation. Diffusion and convection are the two main mechanisms that affect gas transport, fate and emissions in the soils and in the upper vadose zone. In this work we studied CO2 soil-atmosphere gas exchange under both day-time and night-time conditions, focusing on the impact of thermal convection (TCV) during the night. Experiments were performed in a climate-controlled laboratory. One meter long columns were packed with matrix of different grain size (sand, gravel and soil aggregates). Air with 2000 ppm CO2 was injected into the bottom of the columns and CO2 concentration within the columns was continuously monitored by an Infra Red Gas Analyzer. Two scenarios were compared for each soil: (1) isothermal conditions, representing day time conditions; and (2) thermal gradient conditions, i.e., atmosphere colder than the soil, representing night time conditions. Our results show that under isothermal conditions, diffusion is the major mechanism for surface-atmosphere gas exchange for all grain sizes; while under night time conditions the prevailing mechanism is dependent on the air permeability of the matrix: for sand and gravel it is diffusion, and for soil aggregates it is TCV. Calculated CO2 flux for the soil aggregates column shows that the TCV flux was three orders of magnitude higher than the diffusive flux.

  3. FDMH - The tritium model in RODOS

    International Nuclear Information System (INIS)

    Galeriu, D.; Mateescu, G.; Melintescu, A.; Turcanu, C.; Raskob, W.

    2000-01-01

    intensively use of interdisciplinary research. It is developed in a modular structure with a variable time grid according with the physical processes. During the release phase, the transfer processes are modelled with a half hour time step using real time meteorological data, whereas in the next few days weather forecast data are used at a 2-3 hour interval. In the long term prognosis, a site specific synoptic data file is used and the transfer rates are weekly or monthly averaged. Different from other models, using generic transfer parameters or parameters fitted on individual experiments, FDMH derives tritium transfer rates based on physical and physiological process analysis, using scientifically accepted results from interdisciplinary research on among others, land-atmosphere interaction, water cycle in the soil-plant-atmosphere system, plant physiology, photosynthesis and growth and hydrogen metabolism in mammals. A unique feature of FDMH is the coherent modelling of tritium uptake by plant canopies and its conversion to organic matter, using a physiological plant parameters data base which can reproduce plant growth under various pedo-climatic conditions. Furthermore, in order to predict tritium transfer in animal products, in the absence of a complete experimental data base, results from basic research on hydrogen metabolism in mammals is applied. Due to this novel approach, FDMH can be easily customised for any European site and can predict the time evolution of tritiated water or organically bound tritium in up to 22 plants, 12 animal products, 35 foodstuff and the public dose for 7 population groups. The code is developed not only under the HP-UNIX platform for RODOS but also as a stand alone PC version which can be easily upgraded for PSA studies in CANDU reactors. Preliminary validation tests of FDMH show remarkable agreement with recent experimental data on tritium transfer in cereals and potato as well as in cow's milk. Future effort is related to customise the

  4. Confinement and Tritium Stripping Systems for APT Tritium Processing

    Energy Technology Data Exchange (ETDEWEB)

    Hsu, R.H. [Westinghouse Savannah River Company, AIKEN, SC (United States); Heung, L.K.

    1997-10-20

    This report identifies functions and requirements for the tritium process confinement and clean-up system (PCCS) and provides supporting technical information for the selection and design of tritium confinement, clean-up (stripping) and recovery technologies for new tritium processing facilities in the Accelerator for the Production of Tritium (APT). The results of a survey of tritium confinement and clean-up systems for large-scale tritium handling facilities and recommendations for the APT are also presented.

  5. Confinement and Tritium Stripping Systems for APT Tritium Processing

    International Nuclear Information System (INIS)

    Hsu, R.H.; Heung, L.K.

    1997-01-01

    This report identifies functions and requirements for the tritium process confinement and clean-up system (PCCS) and provides supporting technical information for the selection and design of tritium confinement, clean-up (stripping) and recovery technologies for new tritium processing facilities in the Accelerator for the Production of Tritium (APT). The results of a survey of tritium confinement and clean-up systems for large-scale tritium handling facilities and recommendations for the APT are also presented

  6. Tritium monitoring techniques

    International Nuclear Information System (INIS)

    DeVore, J.R.; Buckner, M.A.

    1996-05-01

    As part of their operations, the U.S. Navy is required to store or maintain operational nuclear weapons on ships and at shore facilities. Since these weapons contain tritium, there are safety implications relevant to the exposure of personnel to tritium. This is particularly important for shipboard operations since these types of environments can make low-level tritium detection difficult. Some of these ships have closed systems, which can result in exposure to tritium at levels that are below normally acceptable levels but could still cause radiation doses that are higher than necessary or could hamper ship operations. This report describes the state of the art in commercial tritium detection and monitoring and recommends approaches for low-level tritium monitoring in these environments

  7. A metabolic derivation of tritium transfer factors in animal products

    International Nuclear Information System (INIS)

    Galeriu, D.; Melintescu, A.; Crout, N. M. J.; Bersford, N. A.; Peterson, S. R.; Hess, M. van

    2001-01-01

    Tritium is a potentially important environmental contaminant arising from the nuclear industry. Because tritium is an isotope of hydrogen, its behaviour in the environment is controlled by the behaviour of hydrogen. Chronic releases of tritium to the atmosphere, in particular, will result in tritium-to-hydrogen (T/H) ratios in plants and animals that are more or less in equilibrium with T/H ratios in the air moisture. Tritium is thus a potentially important contaminant of plant and animal food products. The transfer of tritium from air moisture to plants is quite well understood. In contrast, although a number of regulatory agencies have published transfer coefficient values for diet tritium transfer for a limited number of animal products, a fresh evaluation of these transfers needs to be made In this paper we present an approach for the derivation of tritium transfer coefficients which is based on the metabolism of hydrogen in animals in conjunction with experimental data on tritium transfer. The derived transfer coefficients separately account for transfer to and from free (i.e. water) and organically bound tritium. The predicted transfer coefficients are compared to available data independent of model development. Agreement is good, with the exception of the transfer coefficient for transfer from tritiated water to organically bound tritium in ruminants, which may be attributable to the particular characteristics of ruminant digestion. We show that transfer coefficients will vary in response to the metabolic status of an animal (e.g. stage of lactation, digestibility of diet, etc.) and that the use of a single transfer coefficient from diet to animal product is not appropriate for tritium. It is possible to derive concentration ratio values which relate the concentration of tritiated water and organically bound tritium in an animal product to the corresponding concentrations in the animals diet. These concentration ratios are shown to be less subject to

  8. Develop of omni-tritium sample preparation device

    International Nuclear Information System (INIS)

    Tian Junhua; Zheng Min; Zhang Dong

    2008-06-01

    The content of total tritium analysis is required in order to know the tritium contaminated degree of biological samples accurately. But the conversion and collection of organic tritium are difficult. A device to treat total tritium samples was developed. Plant samples were treated by combustion and catalysis. After expelling the free HTO in the samples when heated in abundant oxygen, the samples were ignited. Combustion gas passed the catalysts at 800 degree C and its oxidation was catalyzed, and then the combined tritium in tissues was converted into HTO. HTO was collected by water-cooling tube and condenser. For other samples, HTO was treated and collected by high temperature (The highest temperature is 1000 degree C)-catalysis-double condensation method. This device had solved the problem that organic tritium is difficult to gather. (authors)

  9. Measurements of tritium retention and removal on TFTR

    International Nuclear Information System (INIS)

    Skinner, C.H.; Blanchard, W.; Kamperschroer, J.

    1996-05-01

    Recent experiments on the Tokamak Fusion Test Reactor (TFTR) have afforded an opportunity to measure the retention of tritium in a graphite limiter that is subject to erosion, codeposition and high neutron flux. The tritium was injected by both gas puff and neutral beams. The isotopic mix of hydrogenic recycling was measured spectroscopically and the tritium fraction T/(H+D+T) increased to as high as 75%. Some tritium was pumped out during the experimental run and some removed in a subsequent campaign using various clean-up techniques. While the short term retention of tritium was high, various conditioning techniques were successful in removing ∼ 8,000 Ci and restoring the tritium inventory to a level well below the administrative limit

  10. Under What Conditions Can Equilibrium Gas-Particle Partitioning Be Expected to Hold in the Atmosphere?

    Science.gov (United States)

    Mai, Huajun; Shiraiwa, Manabu; Flagan, Richard C; Seinfeld, John H

    2015-10-06

    The prevailing treatment of secondary organic aerosol formation in atmospheric models is based on the assumption of instantaneous gas-particle equilibrium for the condensing species, yet compelling experimental evidence indicates that organic aerosols can exhibit the properties of highly viscous, semisolid particles, for which gas-particle equilibrium may be achieved slowly. The approach to gas-particle equilibrium partitioning is controlled by gas-phase diffusion, interfacial transport, and particle-phase diffusion. Here we evaluate the controlling processes and the time scale to achieve gas-particle equilibrium as a function of the volatility of the condensing species, its surface accommodation coefficient, and its particle-phase diffusivity. For particles in the size range of typical atmospheric organic aerosols (∼50-500 nm), the time scale to establish gas-particle equilibrium is generally governed either by interfacial accommodation or particle-phase diffusion. The rate of approach to equilibrium varies, depending on whether the bulk vapor concentration is constant, typical of an open system, or decreasing as a result of condensation into the particles, typical of a closed system.

  11. Tritium in metals

    International Nuclear Information System (INIS)

    Schober, T.

    1990-01-01

    In this Chapter a review is given of some of the important features of metal tritides as opposed to hydrides and deuterides. After an introduction to the topics of tritium and tritium in metals information will be presented on a variety of metal-tritium systems. Of main interest here are the differences from the classic hydrogen behavior; the so called isotope effect. A second important topic is that of aging effects produced by the accumulation of 3 He in the samples. (orig.)

  12. Tritium sources; Izvori tricijuma

    Energy Technology Data Exchange (ETDEWEB)

    Glodic, S [Institute of Nuclear Sciences VINCA, Belgrade (Yugoslavia); Boreli, F [Elektrotehnicki fakultet, Belgrade (Yugoslavia)

    1993-07-01

    Tritium is the only radioactive isotope of hydrogen. It directly follows the metabolism of water and it can be bound into genetic material, so it is very important to control levels of contamination. In order to define the state of contamination it is necessary to establish 'zero level', i.e. actual global inventory. The importance of tritium contamination monitoring increases with the development of fusion power installations. Different sources of tritium are analyzed and summarized in this paper. (author)

  13. [Investigation on the gas temperature of a plasma jet at atmospheric pressure by emission spectrum].

    Science.gov (United States)

    Li, Xue-chen; Yuan, Ning; Jia, Peng-ying; Niu, Dong-ying

    2010-11-01

    A plasma jet of a dielectric barrier discharge in coaxial electrode was used to produce plasma plume in atmospheric pressure argon. Spatially and temporally resolved measurement was carried out by photomultiplier tubes. The light emission signals both from the dielectric barrier discharge and from the plasma plume were analyzed. Furthermore, emission spectrum from the plasma plume was collected by high-resolution optical spectrometer. The emission spectra of OH (A 2sigma + --> X2 II, 307.7-308.9 nm) and the first negative band of N2+ (B2 sigma u+ --> X2 IIg+, 390-391.6 nm) were used to estimate the rotational temperature of the plasma plume by fitting the experimental spectra to the simulated spectra. The rotational temperature obtained is about 443 K by fitting the emission spectrum from the OH, and that from the first negative band of N2+ is about 450 K. The rotational temperatures obtained by the two method are consistent within 5% error band. The gas temperature of the plasma plume at atmospheric pressure was obtained because rotational temperature equals to gas temperature approximately in gas discharge at atmospheric pressure. Results show that gas temperature increases with increasing the applied voltage.

  14. Tritium distribution in leachates from domestic solid waste landfills

    International Nuclear Information System (INIS)

    Park, Soon Dal; Kim, Jung Suk; Joe, Kih Soo; Kim, Jong Gu; Kim, Won Ho

    2004-01-01

    It is for the purpose of investigating the tritium distribution in the leachates, the raw and treated leachates and the condensates of the methane gas, which have occurred from domestic solid waste landfills. Also it aims to measure the tritium distribution level on the colloid size of the leachates, the raw and treated leachates. It was found that the major inorganic contaminants of the leachates were Na, K, Ca, Mg, NH 4 + -N and Cl - . The mean tritium level of the raw leachates of the investigated 13 landfill sites for 6 months was 17∼1196 TU. It corresponded to a several scores or hundreds of magnitude higher value than that of the normal environmental sample level except for two landfill sites. Also such a high concentration of the tritium was found in the treated leachates and methane gas condensates as well. Nevertheless it is important to emphasize that the tritium level which was found in this research is about 100 times lower than the tritium limit for the drinking water quality. And most of the tritium existed in the dissolved colloid of the leachate of which the colloid size is below 0.45 μm. Also, according to the tritium analysis results of the leachates after filtration with 0.45μm membrane filter for some landfills, it is likely that some tritium of the leachate would be distributed in a colloid size over 0.45μm. In general the relationship between the tritium and other contaminants in the raw leachate was low, but it was relatively high between the tritium and TOC. However, the tritium content in the leachate had no meaningful relationship with the scale, hydrological characteristics and age of the landfill

  15. Tritium evolution from various morphologies of palladium

    International Nuclear Information System (INIS)

    Tuggle, D.G.; Claytor, T.N.; Taylor, S.F.

    1994-01-01

    The authors have been able to extend the tritium production techniques to various novel morphologies of palladium. These include small solid wires of various diameters and a type of pressed powder wire and a plasma cell. In most successful experiments, the amount of palladium required, for an equivalent tritium output, has been reduced by a factor of 100 over the older powder methods. In addition, they have observed rates of tritium production (>5 nCi/h) that far exceed most of the previous results. Unfortunately, the methods that they currently use to obtain the tritium are poorly understood and consequently there are numerous variables that need to be investigated before the new methods are as reliable and repeatable as the previous techniques. For instance, it seems that surface and/or bulk impurities play a major role in the successful generation of any tritium. In those samples with total impurity concentrations of >400 ppM essentially no tritium has been generated by the gas loading and electrical simulation methods

  16. Tritium: an underestimated health risk- 'ACROnic du nucleaire' nr 85, June 2009

    International Nuclear Information System (INIS)

    Barbey, Pierre

    2009-06-01

    After having indicated how tritium released in the environment (under the form of tritiated water or gas) is absorbed by living species, the author describes the different biological effects of ionizing radiations and the risk associated with tritium. He evokes how the radiation protection system is designed with respect to standards, and outlines how the risk related to tritium is underestimated by different existing models and standards. The author discusses the consequences of tritium transmutation and of the isotopic effect

  17. Atmospheric-pressure dielectric barrier discharge with capillary injection for gas-phase nanoparticle synthesis

    International Nuclear Information System (INIS)

    Ghosh, Souvik; Liu, Tianqi; Bilici, Mihai; Cole, Jonathan; Huang, I-Min; Sankaran, R Mohan; Staack, David; Mariotti, Davide

    2015-01-01

    We present an atmospheric-pressure dielectric barrier discharge (DBD) reactor for gas-phase nanoparticle synthesis. Nickel nanoparticles are synthesized by homogenous nucleation from nickelocene vapor and characterized online by aerosol mobility measurements. The effects of residence time and precursor concentration on particle growth are studied. We find that narrower distributions of smaller particles are produced by decreasing the precursor concentration, in agreement with vapor nucleation theory, but larger particles and aggregates form at higher gas flow rates where the mean residence time should be reduced, suggesting a cooling effect that leads to enhanced particle nucleation. In comparison, incorporating a capillary gas injector to alter the velocity profile is found to significantly reduce particle size and agglomeration. These results suggest that capillary gas injection is a better approach to decreasing the mean residence time and narrowing the residence time distribution for nanoparticle growth by producing a sharp and narrow velocity profile. (paper)

  18. Spatial distribution of tritium in the Rawatbhata Rajasthan site environment

    International Nuclear Information System (INIS)

    GilI, Rajpal; Tiwari, S.N.; Gocher, A.K.; Ravi, P.M.; Tripathi, R.M.

    2014-01-01

    Tritium is one of the most environmentally mobile radionuclides and hence has high potential for migration into the different compartments of environment. Tritium from nuclear facilities at RAPS site is released into the environment through 93 m and 100 m high stack mainly as tritiated water (HTO). The released tritium undergoes dilution and dispersion and then follows the ecological pathway of water molecule. Environmental Survey Laboratory of Health Physics Division, Bhabha Atomic Research Centre (BARC), located at Rajasthan Atomic Power Station (RAPS) site is continuously monitoring the concentration of tritium in the environment to ensure the public safety. Atmospheric tritium activity during the period (2009-2013) was measured regularly around Rajasthan Atomic Power Station (RAPS). Data collected showed a large variation of H-3 concentration in air fluctuating in the range of 0.43 - 5.80 Bq.m -3 at site boundary of 1.6 km. This paper presents the result of analyses of tritium in atmospheric environment covering an area up to 20 km radius around RAPS site. Large number of air moisture samples were collected around the RAPS site, for estimating tritium in atmospheric environment to ascertain the atmospheric dispersion and computation of radiation dose to the public

  19. Electric field measurement in an atmospheric or higher pressure gas by coherent Raman scattering of nitrogen

    International Nuclear Information System (INIS)

    Ito, Tsuyohito; Kobayashi, Kazunobu; Hamaguchi, Satoshi; Mueller, Sarah; Luggenhoelscher, Dirk; Czarnetzki, Uwe

    2009-01-01

    The feasibility of electric field measurement based on field-induced coherent Raman scattering is demonstrated for the first time in a nitrogen containing gas at atmospheric or higher pressure, including open air. The technique is especially useful for the determination of temporal and spatial profiles of the electric field in air-based microdischarges, where nitrogen is abundant. In our current experimental setup, the minimum detectable field strength in open air is about 100 V mm -1 , which is sufficiently small compared with the average field present in typical microdischarges. No further knowledge of other gas/plasma parameters such as the nitrogen density is required. (fast track communication)

  20. Microkinetics of H2S Removal by Zinc Oxide in the Presence of Moist Gas Atmosphere

    Institute of Scientific and Technical Information of China (English)

    Huiling Fan; Chunhu Li; Hanxian Guo; Kechang Xie

    2003-01-01

    The microkinetics of H2S removal by ZnO desulfurization in H2O-CO2-N2, H2O-CO-N2 andH2O-O2-N2 gas mixtures was studied by thermogravimetric analysis. Experiments were carried out with100 120 mesh ZnO powder at temperatures from 473 K to 563 K. The results show that the kineticbehaviors of desulfurization could all be described by an improved shrinking-core model. The activationenergies of the reaction and the diffusion in different gas atmospheres were estimated.

  1. Effect of Tritium on Cracking Threshold in 7075 Aluminum

    Energy Technology Data Exchange (ETDEWEB)

    Duncan, A. [Savannah River Site (SRS), Aiken, SC (United States). Savannah River National Lab. (SRNL); Morgan, M. [Savannah River Site (SRS), Aiken, SC (United States). Savannah River National Lab. (SRNL)

    2017-02-28

    The effect of long-term exposure to tritium gas on the cracking threshold (KTH) of 7075 Aluminum Alloy was investigated. The alloy is the material of construction for a cell used to contain tritium in an accelerator at Jefferson Laboratory designed for inelastic scattering experiments on nucleons. The primary safety concerns for the Jefferson Laboratory tritium cell is a tritium leak due to mechanical failure of windows from hydrogen isotope embrittlement, radiation damage, or loss of target integrity from accidental excessive beam heating due to failure of the raster or grossly mis-steered beam. Experiments were conducted to investigate the potential for embrittlement of the 7075 Aluminum alloy from tritium gas.

  2. Propagation of atmospheric pressure helium plasma jet into ambient air at laminar gas flow

    International Nuclear Information System (INIS)

    Pinchuk, M; Kurakina, N; Spodobin, V; Stepanova, O

    2017-01-01

    The formation of an atmospheric pressure plasma jet (APPJ) in a gas flow passing through the discharge gap depends on both gas-dynamic properties and electrophysical parameters of the plasma jet generator. The paper presents the results of experimental and numerical study of the propagation of the APPJ in a laminar flow of helium. A dielectric-barrier discharge (DBD) generated inside a quartz tube equipped with a coaxial electrode system, which provided gas passing through it, served as a plasma source. The transition of the laminar regime of gas flow into turbulent one was controlled by the photography of a formed plasma jet. The corresponding gas outlet velocity and Reynolds numbers were revealed experimentally and were used to simulate gas dynamics with OpenFOAM software. The data of the numerical simulation suggest that the length of plasma jet at the unvarying electrophysical parameters of DBD strongly depends on the mole fraction of ambient air in a helium flow, which is established along the direction of gas flow. (paper)

  3. Propagation of atmospheric pressure helium plasma jet into ambient air at laminar gas flow

    Science.gov (United States)

    Pinchuk, M.; Stepanova, O.; Kurakina, N.; Spodobin, V.

    2017-05-01

    The formation of an atmospheric pressure plasma jet (APPJ) in a gas flow passing through the discharge gap depends on both gas-dynamic properties and electrophysical parameters of the plasma jet generator. The paper presents the results of experimental and numerical study of the propagation of the APPJ in a laminar flow of helium. A dielectric-barrier discharge (DBD) generated inside a quartz tube equipped with a coaxial electrode system, which provided gas passing through it, served as a plasma source. The transition of the laminar regime of gas flow into turbulent one was controlled by the photography of a formed plasma jet. The corresponding gas outlet velocity and Reynolds numbers were revealed experimentally and were used to simulate gas dynamics with OpenFOAM software. The data of the numerical simulation suggest that the length of plasma jet at the unvarying electrophysical parameters of DBD strongly depends on the mole fraction of ambient air in a helium flow, which is established along the direction of gas flow.

  4. Tritium management in fusion reactors

    International Nuclear Information System (INIS)

    Galloway, T.R.

    1978-05-01

    This is a review paper covering the key environmental and safety issues and how they have been handled in the various magnetic and inertial confinement concepts and reference designs. The issues treated include: tritium accident analyses, tritium process control, occupational safety, HTO formation rate from the gas-phase, disposal of tritium contaminated wastes, and environmental impact--each covering the Joint European Tokamak (J.E.T. experiment), Tokamak Fusion Test Reactor (TFTR), Russian T-20, The Next Step (TNS) designs by Westinghouse/ORNL and General Atomic/ANL, the ANL and ORNL EPR's, the G.A. Doublet Demonstration Reactor, the Italian Fintor-D and the ORNL Demo Studies. There are also the following full scale plant reference designs: UWMAK-III, LASL's Theta Pinch Reactor Design (RTPR), Mirror Fusion Reactor (MFR), Tandem Mirror Reactor (TMR), and the Mirror Hybrid Reactor (MHR). There are four laser device breakeven experiments, SHIVA-NOVA, LLL reference designs, ORNL Laser Fusion power plant, the German ''Saturn,'' and LLL's Laser Fusion EPR I and II

  5. Gas Breakdown of Radio Frequency Glow Discharges in Helium at near Atmospheric Pressure

    International Nuclear Information System (INIS)

    Liu Xinkun; Xu Jinzhou; Cui Tongfei; Guo Ying; Zhang Jing; Shi Jianjun

    2013-01-01

    A one-dimensional self-consistent fluid model was developed for radio frequency glow discharge in helium at near atmospheric pressure, and was employed to study the gas breakdown characteristics in terms of breakdown voltage. The effective secondary electron emission coefficient and the effective electric field for ions were demonstrated to be important for determining the breakdown voltage of radio frequency glow discharge at near atmospheric pressure. The constant of A was estimated to be 64±4 cm −1 Torr −1 , which was proportional to the first Townsend coefficient and could be employed to evaluate the gas breakdown voltage. The reduction in the breakdown voltage of radio frequency glow discharge with excitation frequency was studied and attributed to the electron trapping effect in the discharge gap

  6. Statistical Analysis of Environmental Tritium around Wolsong Site

    Energy Technology Data Exchange (ETDEWEB)

    Kim, Ju Youl [FNC Technology Co., Yongin (Korea, Republic of)

    2010-04-15

    To find the relationship among airborne tritium, tritium in rainwater, TFWT (Tissue Free Water Tritium) and TBT (Tissue Bound Tritium), statistical analysis is conducted based on tritium data measured at KHNP employees' house around Wolsong nuclear power plants during 10 years from 1999 to 2008. The results show that tritium in such media exhibits a strong seasonal and annual periodicity. Tritium concentration in rainwater is observed to be highly correlated with TFWT and directly transmitted to TFWT without delay. The response of environmental radioactivity of tritium around Wolsong site is analyzed using time-series technique and non-parametric trend analysis. Tritium in the atmosphere and rainwater is strongly auto-correlated by seasonal and annual periodicity. TFWT concentration in pine needle is proven to be more sensitive to rainfall phenomenon than other weather variables. Non-parametric trend analysis of TFWT concentration within pine needle shows a increasing slope in terms of confidence level of 95%. This study demonstrates a usefulness of time-series and trend analysis for the interpretation of environmental radioactivity relationship with various environmental media.

  7. Distribution of tritium in water vapour and precipitation around Wolsung nuclear power plant.

    Science.gov (United States)

    Chae, Jung-Seok; Lee, Sang-Kuk; Kim, Yongjae; Lee, Jung-Min; Cho, Heung-Joon; Cho, Yong-Woo; Yun, Ju-Yong

    2011-07-01

    The distribution of tritium in water vapour and precipitation with discharge of tritiated water vapour and meteorological factors was studied around the Wolsung nuclear power plant (NPP) site during the period 2004-2008. The tritium concentrations in atmospheric water vapour and precipitation had a temporal variation with relatively high values in the early summer. Spatial distribution of tritium concentrations was affected by various factors such as distance from the NPP site, wind direction, tritium discharge into the atmosphere and atmospheric dispersion factor. The annual mean concentrations of atmospheric HTO and precipitation were correlated with the amount of gaseous tritium released from the Wolsung NPP. The tritium concentrations in precipitation decrease exponentially with an increase of the distance from the Wolsung NPP site.

  8. Tritium conversion in tritiated water: study of the involved reactions: a literature survey

    International Nuclear Information System (INIS)

    Ballereau, P.

    1987-10-01

    According to ICRP publication 30, hazards due to molecular tritium are not significant in comparison to hazards due to the oxidated form: tritiated water. It is thus important to know the kinetics of tritium/tritiated water conversion to obtain a realistic evaluation of the risks for the environment at level of present facilities and of future nuclear fusion facilities. Laboratory experiments in static contained conditions have shown that tritiated water is produced by two mechanisms: gas phase oxidation, hydrogen isotopic exchange with water. The periods found are relatively long and difficult to specify. In terrestrial atmosphere, the two mechanisms intervening in tritiated water formation are photochemical oxidation and biochemical reactions occurring in soil and in vegetation aerial parts. The corresponding periods are of some years for the first one, of some hours for the second one [fr

  9. Influence of neutron irradiation on the tritium retention in beryllium

    Energy Technology Data Exchange (ETDEWEB)

    Rolli, R.; Ruebel, S.; Werle, H. [Forschungszentrum Karlsruhe, Inst. fuer Neutronenphysik und Reaktortechnik, Karlsruhe (Germany); Wu, C.H.

    1998-01-01

    Carbon-based materials and beryllium are the candidates for protective layers on the components of fusion reactors facing plasma. In contact with D-T plasma, these materials absorb tritium, and it is anticipated that tritium retention increases with the neutron damage due to neutron-induced traps. Because of the poor data base for beryllium, the work was concentrated on it. Tritium was loaded into the samples from stagnant T{sub 2}/H{sub 2} atmosphere, and afterwards, the quantity of the loaded tritium was determined by purged thermal annealing. The specification of the samples is shown. The samples were analyzed by SEM before and after irradiation. The loading and the annealing equipments are contained in two different glove boxes with N{sub 2} inert atmosphere. The methods of loading and annealing are explained. The separation of neutron-produced and loaded tritium and the determination of loaded tritium in irradiated samples are reported. Also the determination of loaded tritium in unirradiated samples is reported. It is evident that irradiated samples contained much more loaded tritium than unirradiated samples. The main results of this investigation are summarized in the table. (K.I.)

  10. TA [2] Continuous, regional methane emissions estimates in northern Pennsylvania gas fields using atmospheric inversions

    Energy Technology Data Exchange (ETDEWEB)

    Lauvaux, Thomas [Pennsylvania State Univ., University Park, PA (United States)

    2017-12-31

    Natural Gas (NG) production activities in the northeastern Marcellus shale have significantly increased in the last decade, possibly releasing large amounts of methane (CH4) into the atmosphere from the operations at the productions sites and during the processing and transmission steps of the natural gas chain. Based on an intensive aircraft survey, leakage rates from the NG production were quantified in May 2015 and found to be in the order of 0.5% of the total production, higher than reported by the Environmental Protection Agency (EPA) but below the usually observed leakage rates over the shale gases in the US. Thanks to the high production rates on average at each well, leakage rates normalized by production appeared to be low in the northeastern Marcellus shale. This result confirms that natural gas production using unconventional techniques in this region is emitting relatively less CH4 into the atmosphere than other shale reservoirs. The low emissions rate can be explained in part by the high productivity of wells drilled across the northeastern Marcellus region. We demonstrated here that atmospheric monitoring techniques can provide an independent quantification of NG leakage rates using aircraft measurements. The CH4 analyzers were successfully calibrated at four sites across the region, measuring continuously the atmospheric CH4 mixing ratios and isotopic 13Ch4. Our preliminary findings confirm the low leakage rates from tower data collected over September 2015 to November 2016 compared to the aircraft mass-balance estimates in may 2015. However, several episodes revealing large releases of natural gas over several weeks showed that temporal variations in the emissions of CH4 may increase the actual leakage rate over longer time periods.

  11. An Atmosphere-based Method for Detection and Quantification of Methane Emisions from Natural Gas Infrastructure in an Urban Environment

    Science.gov (United States)

    McKain, K.; Down, A.; Raciti, S. M.; Budney, J.; Hutyra, L.; Floerchinger, C. R.; Herndon, S. C.; Nehrkorn, T.; Zahniser, M. S.; Sargent, M. R.; Jackson, R. B.; Phillips, N. G.; Wofsy, S. C.

    2015-12-01

    Methane emissions from the natural gas supply-chain are highly uncertain and can vary widely among components and processes. We present an atmosphere-based method for detecting and quantifying the area and time-averaged surface flux of methane from natural gas infrastructure, and its application to the case-study of Boston, Massachusetts. Continuous measurements of atmospheric methane at a network of stations, inside and outside the city, are used to quantify the atmospheric methane gradient due to emissions from the urban area. Simultaneous observations of atmospheric ethane, and data on the ethane and methane content of the pipeline gas flowing through the region, are used to trace the atmospheric methane enhancement to the natural gas source. An atmospheric transport model is used to quantitatively relate the observed methane enhancement to a surface flux from the whole urban region. We find that methane emissions from natural gas in the urban region over one year was equal to 2.7 ± 0.6 % of the natural gas delivered to the region. Our findings for Boston suggest natural-gas-consuming regions, generally, may be larger sources of methane to the atmosphere than is current estimated and represent areas of significant resource loss.

  12. In-vessel tritium

    International Nuclear Information System (INIS)

    Ueda, Yoshio; Ohya, Kaoru; Ashikawa, Naoko; Ito, Atsushi M.; Kato, Daiji; Kawamura, Gakushi; Takayama, Arimichi; Tomita, Yukihiro; Nakamura, Hiroaki; Ono, Tadayoshi; Kawashima, Hisato; Shimizu, Katsuhiro; Takizuka, Tomonori; Nakano, Tomohide; Nakamura, Makoto; Hoshino, Kazuo; Kenmotsu, Takahiro; Wada, Motoi; Saito, Seiki; Takagi, Ikuji; Tanaka, Yasunori; Tanabe, Tetsuo; Yoshida, Masafumi; Toma, Mitsunori; Hatayama, Akiyoshi; Homma, Yuki; Tolstikhina, Inga Yu.

    2012-01-01

    The in-vessel tritium research is closely related to the plasma-materials interaction. It deals with the edge-plasma-wall interaction, the wall erosion, transport and re-deposition of neutral particles and the effect of neutral particles on the fuel recycling. Since the in-vessel tritium shows a complex nonlinear behavior, there remain many unsolved problems. So far, behaviors of in-vessel tritium have been investigated by two groups A01 and A02. The A01 group performed experiments on accumulation and recovery of tritium in thermonuclear fusion reactors and the A02 group studied theory and simulation on the in-vessel tritium behavior. In the present article, outcomes of the research are reviewed. (author)

  13. Tritium Systems Test Assembly operator training program

    International Nuclear Information System (INIS)

    Kerstiens, F.L.

    1985-01-01

    Proper operator training is needed to help ensure the safe operation of fusion facilities by personnel who are qualified to carry out their assigned responsibilities. Operators control and monitor the Tritium Systems Test Assembly (TSTA) during normal, emergency, and maintenance phases. Their performance is critical both to operational safety, assuring no release of tritium to the atmosphere, and to the successful simulation of the fusion reaction progress. Through proper training we are helping assure that TSTA facility operators perform their assignments in a safe and efficient manner and that the operators maintain high levels of operational proficiency through continuing training, retraining, requalification, and recertification

  14. The Shoreline Environment Atmospheric Dispersion Experiment (SEADEX): Meteorological and gas tracer data

    International Nuclear Information System (INIS)

    Johnson, W.B.; Cantrell, B.K.; Morley, B.M.; Uthe, E.E.; Nitz, K.C.

    1987-10-01

    The SEADEX atmospheric dispersion field study was conducted during the period May 28 to June 8, 1982, in northeastern Wisconsin, the vicinity of the Kewaunee Power Plant on the western shore of Lake Michigan. The specific objectives of SEADEX were to characterize (1) the atmospheric dispersion and (2) the meteorological conditions influencing this dispersion as completely as possible during the test period. This field study included a series of controlled tracer tests utilizing state-of-the-art tracer measurement technology to determine horizontal and vertical dispersion over both land and water. Extensive meteorological measurements were obtained to thoroughly characterize the three-dimensional structure of the atmospheric boundary controlling the dispersion process. This volume presents the meteorological and gas tracer data collected during the field study. 391 figs., 32 tabs

  15. Tritium monitor calibration at Los Alamos National Laboratory

    International Nuclear Information System (INIS)

    Bjork, C.J.; Aikin, D.J.; Houlton, T.W.

    1997-08-01

    Tritium in air is monitored at Los Alamos National Laboratory (LANL) with air breathing instruments based on ionization chambers. Stack emissions are continuously monitored from sample tubes which each connect to a Tritium bubble which differentially collects HTO and HT. A set of glass vials of glycol capture the HTO. The HT is oxidized with a palladium catalyst and the resultant HTO is captured in a second set of vials of glycol. The glycol is counted with a liquid scintillation counter. All calibrations are performed with tritium containing gas. The Radiation Instrumentation and Calibration (RIC) Team has constructed and maintains two closed loop gas handling systems based on femto TECH model U24 tritium ion chamber monitors: a fixed system housed in a fume hood and a portable system mounted on two two wheeled hand trucks. The U24 monitors are calibrated against tritium in nitrogen gas standards. They are used as standard transfer instruments to calibrate other ion chamber monitors with tritium in nitrogen, diluted with air. The gas handling systems include a circulation pump which permits a closed circulation loop to be established among the U24 monitor and typically two to four other monitors of a given model during calibration. Fixed and portable monitors can be calibrated. The stack bubblers are calibrated in the field by: blending a known concentration of tritium in air within the known volume of the two portable carts, coupled into a common loop; releasing that gas mixture into a ventilation intake to the stack; collecting oxidized tritium in the bubbler; counting the glycol; and using the stack and bubbler flow rates, computing the bubbler's efficiency. Gas calibration has become a convenient and quality tool in maintaining the tritium monitors at LANL

  16. Development of Diesel Engine Operated Forklift Truck for Explosive Gas Atmospheres

    Science.gov (United States)

    Vishwakarma, Rajendra Kumar; Singh, Arvind Kumar; Ahirwal, Bhagirath; Sinha, Amalendu

    2018-02-01

    For the present study, a prototype diesel engine operated Forklift truck of 2 t capacity is developed for explosive gas atmosphere. The parts of the Forklift truck are assessed against risk of ignition of the explosive gases, vapors or mist grouped in Gr. IIA and having ignition temperature more than 200°C. Identification of possible sources of ignition and their control or prevention is the main objective of this work. The design transformation of a standard Forklift truck into a special Forklift truck is made on prototype basis. The safety parameters of the improved Forklift truck are discussed in this paper. The specially designed Forklift truck is useful in industries where explosive atmospheres may present during normal working conditions and risk of explosion is a concern during handling or transportation of materials. This indigenous diesel engine based Forklift truck for explosive gas atmosphere classified as Zone 1 and Zone 2 area and gas group IIA is developed first time in India in association with the Industry.

  17. Soil-atmosphere trace gas exchange in semiarid and arid zones.

    Science.gov (United States)

    Galbally, Ian E; Kirstine, Wayne V; Meyer, C P Mick; Wang, Ying Ping

    2008-01-01

    A review is presented on trace gas exchange of CH4, CO, N2O, and NOx arising from agriculture and natural sources in the world's semiarid and arid zones due to soil processes. These gases are important contributors to the radiative forcing and the chemistry of the atmosphere. Quantitative information is summarized from the available studies. Between 5 and 40% of the global soil-atmosphere exchange for these gases (CH4, CO, N2O, and NOx) may occur in semiarid and arid zones, but for each of these gases there are fewer than a dozen studies to support the individual estimates, and these are from a limited number of locations. Significant differences in the biophysical and chemical processes controlling these trace gas exchanges are identified through the comparison of semiarid and arid zones with the moist temperate or wet/dry savanna land regions. Therefore, there is a poorly quantified understanding of the contribution of these regions to the global trace gas cycles and atmospheric chemistry. More importantly, there is a poor understanding of the feedback between these exchanges, global change, and regional land use and air pollution issues. A set of research issues is presented.

  18. Natural gas fugitive emissions rates constrained by global atmospheric methane and ethane.

    Science.gov (United States)

    Schwietzke, Stefan; Griffin, W Michael; Matthews, H Scott; Bruhwiler, Lori M P

    2014-07-15

    The amount of methane emissions released by the natural gas (NG) industry is a critical and uncertain value for various industry and policy decisions, such as for determining the climate implications of using NG over coal. Previous studies have estimated fugitive emissions rates (FER)--the fraction of produced NG (mainly methane and ethane) escaped to the atmosphere--between 1 and 9%. Most of these studies rely on few and outdated measurements, and some may represent only temporal/regional NG industry snapshots. This study estimates NG industry representative FER using global atmospheric methane and ethane measurements over three decades, and literature ranges of (i) tracer gas atmospheric lifetimes, (ii) non-NG source estimates, and (iii) fossil fuel fugitive gas hydrocarbon compositions. The modeling suggests an upper bound global average FER of 5% during 2006-2011, and a most likely FER of 2-4% since 2000, trending downward. These results do not account for highly uncertain natural hydrocarbon seepage, which could lower the FER. Further emissions reductions by the NG industry may be needed to ensure climate benefits over coal during the next few decades.

  19. Atmospheric occurrence, transport and gas-particle partitioning of polychlorinated biphenyls over the northwestern Pacific Ocean

    Science.gov (United States)

    Wu, Zilan; Lin, Tian; Li, Zhongxia; Li, Yuanyuan; Guo, Tianfeng; Guo, Zhigang

    2017-10-01

    Ship-board air samples were collected during March to May 2015 from the East China Sea (ECS) to the northwestern Pacific Ocean (NWP) to explore the atmospheric occurrence and gas-particle partitioning of polychlorinated biphenyls (PCBs) when the westerly East Asian Monsoon prevailed. Total PCB concentrations in the atmosphere ranged from 56.8 to 261 pg m-3. Higher PCB levels were observed off the coast and minor temperature-induced changes showed that continuous emissions from East Asia remain as an important source to the regional atmosphere. A significant relationship between Koa (octanol-air partition coefficient) and KP (gas-particle partition coefficient) for PCBs was observed under continental air masses, suggesting that land-derived organic aerosols affected the PCB gas-particle partitioning after long-range transport, while an absence of this correlation was identified in marine air masses. The PCB partitioning cannot be fully explained by the absorptive mechanism as the predicted KP were found to be 2-3 orders of magnitude lower than the measured Kp, while the prediction was closely matched when soot adsorption was considered. The results suggested the importance of soot carbon as a transport medium for PCBs during their long-range transport and considerable impacts of continental outflows on PCBs across the downwind area. The estimated transport mass of particulate PCBs into the ECS and NWP totals 2333 kg during the spring, constituting ca. 17% of annual emission inventories of unintentionally produced PCB in China.

  20. Gas-to-particle conversion in the atmospheric environment by radiation-induced and photochemical reactions

    International Nuclear Information System (INIS)

    Vohra, K.G.

    1975-01-01

    During the last few years a fascinating new area of research involving ionizing radiations and photochemistry in gas-to-particle conversion in the atmosphere has been developing at a rapid pace. Two problems of major interest and concern in which this is of paramount importance are: (1) radiation induced and photochemical aerosol formation in the stratosphere and, (2) role of radiations and photochemistry in smog formation. The peak in cosmic ray intensity and significant solar UV flux in the stratosphere lead to complex variety of reactions involving major and trace constituents in this region of the atmosphere, and some of these reactions are of vital importance in aerosol formation. The problem is of great current interest because the pollutant gases from industrial sources and future SST operations entering the stratosphere could increase the aerosol burden in the stratosphere and affect the solar energy input of the troposphere with consequent ecological and climatic changes. On the other hand, in the nuclear era, the atmospheric releases from reactors and processing plants could lead to changes in the cloud nucleation behaviour of the environment and possible increase in smog formation in the areas with significant levels of radiations and conventional pollutants. A review of the earlier work, current status of the problem, and conventional pollutants. A review of the earlier work, current status of the problem, and some recent results of the experiments conducted in the author's laboratory are presented. The possible mechanisms of gas-to-particle conversion in the atmosphere have been explained

  1. Tritium fuel cycle modeling and tritium breeding analysis for CFETR

    Energy Technology Data Exchange (ETDEWEB)

    Chen, Hongli; Pan, Lei; Lv, Zhongliang; Li, Wei; Zeng, Qin, E-mail: zengqin@ustc.edu.cn

    2016-05-15

    Highlights: • A modified tritium fuel cycle model with more detailed subsystems was developed. • The mean residence time method applied to tritium fuel cycle calculation was updated. • Tritium fuel cycle analysis for CFETR was carried out. - Abstract: Attaining tritium self-sufficiency is a critical goal for fusion reactor operated on the D–T fuel cycle. The tritium fuel cycle models were developed to describe the characteristic parameters of the various elements of the tritium cycle as a tool for evaluating the tritium breeding requirements. In this paper, a modified tritium fuel cycle model with more detailed subsystems and an updated mean residence time calculation method was developed based on ITER tritium model. The tritium inventory in fueling system and in plasma, supposed to be important for part of the initial startup tritium inventory, was considered in the updated mean residence time method. Based on the model, the tritium fuel cycle analysis of CFETR (Chinese Fusion Engineering Testing Reactor) was carried out. The most important two parameters, the minimum initial startup tritium inventory (I{sub m}) and the minimum tritium breeding ratio (TBR{sub req}) were calculated. The tritium inventories in steady state and tritium release of subsystems were obtained.

  2. GASFLOW analysis of a tritium leak accident

    International Nuclear Information System (INIS)

    Farman, R.F.; Fujita, R.K.; Travis, J.R.

    1994-01-01

    The consequences of an earthquake-induced fire involving a tritium leak were analyzed using the GASFLOW computer code. Modeling features required by the analysis include ventilation boundary conditions, flow of a gas mixture in an enclosure containing obstacles, thermally induced buoyancy, and combustion phenomena. (author). 2 refs., 6 figs

  3. GASFLOW analysis of a tritium leak accident

    International Nuclear Information System (INIS)

    Farman, R.F.; Fujita, R.K.; Travis, J.R.

    1994-01-01

    The consequences of an earthquake-induced fire involving a tritium leak were analyzed using the GASFLOW computer code. Modeling features required by the analysis include ventilation boundary conditions, flow of a gas mixture in an enclosure containing obstacles, thermally induced buoyancy, and combustion phenomena

  4. Analytic of tritium-containing gaseous species at the Tritium Laboratory Karlsruhe

    International Nuclear Information System (INIS)

    Laesser, R.; Caldwell-Nichols, C.; Doerr, L.; Glugla, M.; Gruenhagen, S.; Guenther, K.; Penzhorn, R.-D.

    2001-01-01

    At the Tritium Laboratory Karlsruhe (TLK) laser Raman spectroscopy, gas chromatography, mass spectroscopy, calorimetry and ionisation chambers are used to determine the composition of tritium gas mixtures. For the first time a laser Raman experiment was assembled with an actively controlled resonator which yields a 50 times higher Raman signal and with all components (laser, optics, Raman cell and spectrometer) installed inside a glove box. Three gas chromatographs, each with up to six detectors, can determine the gases and their tritiated fractions expected in fusion devices down to the sub-ppm range. Tritium in solids, liquids and gases is determined by means of three calorimeters with a dynamic ranges of up to five orders of magnitude and a lower detection limit of 1 GBq. Since any of these techniques has its shortcomings the best analytical approach is to analyse a sample by more than one method

  5. Environmental Aspects of Tritium Around the Vinca Institute of Nuclear Sciences

    International Nuclear Information System (INIS)

    Miljevic, N.; Sipka, V.

    1995-01-01

    An overview of environmental distribution of tritium around the Institute of Nuclear Sciences Vinca during the period 1988-1994 is presented. Temporal and local variations of the specific tritium variations in precipitation (Usek, Zeleno Brdo), river waters (the Danube, the Sava and Mlaka Creek) as well as atmospheric water vapor are given. Estimates based on precipitation measurements have shown that 6.3 TBq of tritium activity should be released annually into the atmosphere from the Vinca Institute of Nuclear Sciences. (author)

  6. Development of organic tritium light technology at Ontario Hydro

    International Nuclear Information System (INIS)

    Mullins, D.F.; Krasznai, J.P.; Mueller, D.A.

    1992-01-01

    Tritium is a by-product of CANDU heavy water reactor operations and is the major contributor to internal dose for plant workers. The Darlington Tritium Removal Facility (DTRF) is decontaminating heavy water by removing tritium and storing it as a metal hydride. In view of the large tritium separation capacity, (24 MCi/a, 888 PBq/a). This paper reports that Ontario Hydro is interested in pursuing markets for the peaceful uses of tritium. One of these peaceful uses is in self-luminous lighting. The state of the art at present is a phosphor coated tube filled with tritium gas. However, safety considerations have restricted the use of these lights to outdoor or essential safety applications. Binding the tritium to a solid non-volatile matrix would increase the safety of tritium lights and allow the use of other phosphors, matrices and construction geometries. Solid, organic based tritium lights were produced using two different polymer matrices. While both these materials produced visible light, the intensity was low and radiolytic damage to the polymers was evident

  7. Results of monitoring of tritium behaviour and its concentration in the objects of Chernobylsk NPP environment

    International Nuclear Information System (INIS)

    Badyaev, V.V.; Egorov, Yu.A.; Korobejnikov, V.L.; Krasnozhen, G.N.; Stegachev, G.F.; Tolstykh, V.D.

    1985-01-01

    Results of systematic observations on tritium behaviur at the Chernobyl NPP in the system ''source of formation-environment'' are presented. Investigations were conducted in a stepwise manner. Investigations of the first step were performed in order to make an experimental basis of the tritium dynamic model. Tritium activity is determined in all NPP technological subsystems, in cooling reservoir and in the atmosphere. The dynamic model of tritium accumulation at NPP with LWGR-reactor and its exchange with environment is developed and studied at the second step. The third step of investigations includes studies of tritium behaviour in complex experiments along with the behaviour of other radionuclides present in NPP releases and effluents incidentally state of environmental objects is recorded. It is shown that tritium specific activity in atmosphere does not exceed the background values. Tritium activity in leaves of trees is equal to (5-7)x10 -11 Ci/kg of mass

  8. FDNH - the tritium module in RODOS

    International Nuclear Information System (INIS)

    Galeriu, D.; Melintescu, A.; Turcanu, C. O.; Raskob, W.

    2001-01-01

    Under the auspices of its RTD (Research and Technological Development) Framework Programmes, the European Commission has supported the development of the RODOS (Real-time On-line Decision Support) system for off-site emergency management. The project started in 1989 focusing on PWR/LWR type accidents and using experience from the Chernobyl accident. In 1997 it was realised that tritium should be included in the list of radionuclides, as large tritium sources exists in Europe and to allow a potential expansion of the RODOS system for application on future fusion reactor accidents. The National Institute for Physics and Nuclear Engineering (IFIN-HH) in Romania - in close co-operation with the Research Centre Karlsruhe (FZK) - was charged to develop the tritium module, based on previous experience in environmental tritium modelling and the operation of CANDU reactors in Romania (with potential tritium accidents). At present, the Food and Dose Module Hydrogen -(FDMH) - for tritium applications - is integrated and documented in the RODOS system. It calculates the time dependent tritium concentration (as tritiated water or organically bound tritium) in crops (as much as 22 different species) and up to 12 animal products, inhalation doses and ingestion dose from up to 34 diet items for various groups of the population and for up to 2520 locations around the source, following an accidental emission of tritiated water. FDMH incorporates many improved techniques in radiological assessment and makes intensively use of interdisciplinary research. It is developed in a modular structure with a variable time grid according to the physical processes. Differing from other models, using generic transfer parameters or parameters fitted on individual experiments, FDMH derives tritium transfer rates based on physical and physiological process analysis, using scientifically accepted results from interdisciplinary research on, among others, land-atmosphere interaction, water cycle in the

  9. Tritium labelling of molecules constrained in microporous catalysts

    International Nuclear Information System (INIS)

    Long, M.A.; Garnett, J.L.; Than, Chit

    1989-01-01

    The use of microporous aluminophosphate catalysts for exchange between tritium gas or tritiated water and organic substrates is described. The results are compared with those of microporous zeolites. Results are interpreted in terms of the influence of the constraints imposed on molecular configuration by the catalyst pore geometry. The use of these porous structures for minimising byproduct formation in radiation induced labelling processes with tritium gas is described. (author). 10 refs.; 3 tabs

  10. Gas and heat dynamics of a micro-scaled atmospheric pressure plasma reference jet

    International Nuclear Information System (INIS)

    Kelly, Seán; Golda, Judith; Schulz-von der Gathen, Volker; Turner, Miles M

    2015-01-01

    Gas and heat dynamics of the ‘Cooperation on Science and Technology (COST) Reference Microplasma Jet’ (COST-jet), a European lead reference device for low temperature atmospheric pressure plasma application, are investigated. Of particular interest to many biomedical application scenarios, the temperature characteristics of a surface impacted by the jet are revealed. Schlieren imaging, thermocouple measurements, infrared thermal imaging and numerical modelling are employed. Temperature spatial profiles in the gas domain reveal heating primarily of the helium fraction of the gas mixture. Thermocouple and model temporal data show a bounded exponential temperature growth described by a single characteristic time parameter to reach  ∼63% or (1-1/e) fraction of the temperature increase. Peak temperatures occurred in the gas domain where the carrier jet exits the COST-jet, with values ranging from ambient temperatures to in excess of 100 °C in ‘α-mode’ operation. In a horizontal orientation of the COST-jet a curved trajectory of the helium effluent at low gas flows results from buoyant forces. Gas mixture profiles reveal significant containment of the helium concentrations for a surface placed in close proximity to the COST-jet. Surface heating of a quartz plate follows a similar bounded exponential temporal temperature growth as device heating. Spatial profiles of surface heating are found to correlate strongly to the impacting effluent where peak temperatures occur in regions of maximum surface helium concentration. (paper)

  11. Gas and heat dynamics of a micro-scaled atmospheric pressure plasma reference jet

    Science.gov (United States)

    Kelly, Seán; Golda, Judith; Turner, Miles M.; Schulz-von der Gathen, Volker

    2015-11-01

    Gas and heat dynamics of the ‘Cooperation on Science and Technology (COST) Reference Microplasma Jet’ (COST-jet), a European lead reference device for low temperature atmospheric pressure plasma application, are investigated. Of particular interest to many biomedical application scenarios, the temperature characteristics of a surface impacted by the jet are revealed. Schlieren imaging, thermocouple measurements, infrared thermal imaging and numerical modelling are employed. Temperature spatial profiles in the gas domain reveal heating primarily of the helium fraction of the gas mixture. Thermocouple and model temporal data show a bounded exponential temperature growth described by a single characteristic time parameter to reach  ∼63% or (1-1/e) fraction of the temperature increase. Peak temperatures occurred in the gas domain where the carrier jet exits the COST-jet, with values ranging from ambient temperatures to in excess of 100 °C in ‘α-mode’ operation. In a horizontal orientation of the COST-jet a curved trajectory of the helium effluent at low gas flows results from buoyant forces. Gas mixture profiles reveal significant containment of the helium concentrations for a surface placed in close proximity to the COST-jet. Surface heating of a quartz plate follows a similar bounded exponential temporal temperature growth as device heating. Spatial profiles of surface heating are found to correlate strongly to the impacting effluent where peak temperatures occur in regions of maximum surface helium concentration.

  12. Tritium Research Laboratory safety analysis report

    Energy Technology Data Exchange (ETDEWEB)

    Wright, D.A.

    1979-03-01

    Design and operational philosophy has been evolved to keep radiation exposures to personnel and radiation releases to the environment as low as reasonably achievable. Each experiment will be doubly contained in a glove box and will be limited to 10 grams of tritium gas. Specially designed solid-hydride storage beds may be used to store temporarily up to 25 grams of tritium in the form of tritides. To evaluate possible risks to the public or the environment, a review of the Sandia Laboratories Livermore (SLL) site was carried out. Considered were location, population, land use, meteorology, hydrology, geology, and seismology. The risks and the extent of damage to the TRL and vital systems were evaluated for flooding, lightning, severe winds, earthquakes, explosions, and fires. All of the natural phenomena and human error accidents were considered credible, although the extent of potential damage varied. However, rather than address the myriad of specific individual consequences of each accident scenario, a worst-case tritium release caused indirectly by an unspecified natural phenomenon or human error was evaluated. The maximum credible radiological accident is postulated to result from the release of the maximum quantity of gas from one experiment. Thus 10 grams of tritium gas was used in the analysis to conservatively estimate the maximum whole-body dose of 1 rem at the site boundary and a maximum population dose of 600 man-rem. Accidental release of this amount of tritium implies simultaneous failure of two doubly contained systems, an occurrence considered not credible. Nuclear criticality is impossible in this facility. Based upon the analyses performed for this report, we conclude that the Tritium Research Laboratory can be operated without undue risk to employees, the general public, or the environment. (ERB)

  13. Tritium Research Laboratory safety analysis report

    International Nuclear Information System (INIS)

    Wright, D.A.

    1979-03-01

    Design and operational philosophy has been evolved to keep radiation exposures to personnel and radiation releases to the environment as low as reasonably achievable. Each experiment will be doubly contained in a glove box and will be limited to 10 grams of tritium gas. Specially designed solid-hydride storage beds may be used to store temporarily up to 25 grams of tritium in the form of tritides. To evaluate possible risks to the public or the environment, a review of the Sandia Laboratories Livermore (SLL) site was carried out. Considered were location, population, land use, meteorology, hydrology, geology, and seismology. The risks and the extent of damage to the TRL and vital systems were evaluated for flooding, lightning, severe winds, earthquakes, explosions, and fires. All of the natural phenomena and human error accidents were considered credible, although the extent of potential damage varied. However, rather than address the myriad of specific individual consequences of each accident scenario, a worst-case tritium release caused indirectly by an unspecified natural phenomenon or human error was evaluated. The maximum credible radiological accident is postulated to result from the release of the maximum quantity of gas from one experiment. Thus 10 grams of tritium gas was used in the analysis to conservatively estimate the maximum whole-body dose of 1 rem at the site boundary and a maximum population dose of 600 man-rem. Accidental release of this amount of tritium implies simultaneous failure of two doubly contained systems, an occurrence considered not credible. Nuclear criticality is impossible in this facility. Based upon the analyses performed for this report, we conclude that the Tritium Research Laboratory can be operated without undue risk to employees, the general public, or the environment

  14. Tritium stripping in a nitrogen glovebox using SAES St 198

    International Nuclear Information System (INIS)

    Klein, J.E.; Wermer, J.R.

    1994-01-01

    SAES metal getter material St 198 was chosen for glovebox stripper tests to evaluate its effectiveness of removing tritium from a nitrogen atmosphere. The St 198 material is unique from a number of other metal hydride-based getter materials in that it is relatively inert to nitrogen and can thus be used in nitrogen glovebox atmospheres. Six tritium stripper experiments which mock-up the use of a SAES St 198 stripper bed for a full-scale (10,500 liter) nitrogen glovebox have been completed. Experiments consisted of a release of small quantity of protium/deuterium spiked with tritium which were scaled to simulate tritium releases of 0.1 g., 1.0 g., and 10 g. into the glovebox. The tritium spike allows detection using tritium ion chambers. The St 198 stripper system produced a reduction in tritium activity of approximately two orders of magnitude in 24 hours (6--8 atmosphere turn-overs) of stripper operation

  15. Natural gas and quality of fuels for the reduction of atmospheric pollution

    International Nuclear Information System (INIS)

    Riva, A.; Occhio, L.; Andreetto, B.

    1998-01-01

    The production of atmospheric pollutants in combustion processes depends on plant characteristic, combustion conditions and fuel quality. The influence of fuel quality on the emission of sulphur oxides, nitrogen oxides, carbon monoxide, dust and carbon dioxide and on the emission of some toxic pollutants, such as heavy metals and polycyclic aromatic hydrocarbons, is analysed. The comparison between the emission limits, fixed by the Italian legislation, and the uncontrolled pollutant emissions, produced by fossil fuel combustion in power plants and industrial use, shows that, in order to comply with the limits, a reduction of pollutant emissions is required through the use of abatement systems and cleaner fuels where natural gas has a primary role. The use of cleaner fuels is particularly required in heating plants and appliances for the residential sector, where the development of new gas technologies further increases the environmental advantages of natural gas in comparison with other fuels [it

  16. Final programmatic environmental impact statement for tritium supply and recycling

    International Nuclear Information System (INIS)

    1995-10-01

    Tritium, a radioactive gas used in all of the Nation's nuclear weapons, has a short half-life and must be replaced periodically in order for the weapon to operate as designed. Currently, there is no capability to produce the required amounts of tritium within the Nuclear Weapons Complex. The PEIS for Tritium Supply and Recycling evaluates the alternatives for the siting, construction, and operation of tritium supply and recycling facilities at each of five candidate sites: the Idaho National Engineering Laboratory, the Nevada Test Site, the Oak Ridge Reservation, the Pantex Plant, and the Savannah River Site. Alternatives for new tritium supply and recycling facilities consist of four different tritium supply technologies: Heavy Water Reactor, Modular High Temperature Gas-Cooled Reactor, Advanced Light Water Reactor, and Accelerator Production of Tritium. The PEIS also evaluates the impacts of the DOE purchase of an existing operating or partially completed commercial light water reactor or the DOE purchase of irradiation services contracted from commercial power reactors. Additionally, the PEIS includes an analysis of multipurpose reactors that would produce tritium, dispose of plutonium, and produce electricity. Evaluation of impacts on land resources, site infrastructure, air quality and acoustics, water resources, geology and soils, biotic resources, cultural and paleontological resources, socioeconomics, radiological and hazardous chemical impacts during normal operation and accidents to workers and the public, waste management, and intersite transport are included in the assessment

  17. Draft programmatic environmental impact statement for tritium supply and recycling

    International Nuclear Information System (INIS)

    1995-02-01

    Tritium, a radioactive gas used in all of the Nation's nuclear weapons, has a short half-life and must be replaced periodically in order for the weapon to operate as designed. Currently, the Nation has no tritium production capability. The Tritium Supply and Recycling PEIS evaluates the alternatives for the siting, construction, and operation of tritium supply and recycling facilities at each of five candidate sites: the Idaho Engineering Laboratory, the Nevada Test Site, the Oak Ridge Reservation, the Pantex Plant, and the Savannah River Site. Alternatives for new tritium supply and recycling facilities consist of four different tritium supply technologies; Heavy Water Reactor, Modular High Temperature Gas-cooled Reactor, Advanced Light Water Reactor, and Accelerator Production of Tritium. The PEIS also evaluates the impacts of using a commercial light water reactor, either as a contingency in the event of a national emergency or if purchased by the DOE and converted to defense purposes. Additionally, the PEIS includes an analysis of multi-purpose reactors which would produce tritium, dispose of plutonium and produce electricity. Volume I contains the findings of these analyses, Volume II contains the Appendices and supporting data

  18. Tritium breeding in fusion reactors

    International Nuclear Information System (INIS)

    Abdou, M.A.

    1982-10-01

    Key technological problems that influence tritium breeding in fusion blankets are reviewed. The breeding potential of candidate materials is evaluated and compared to the tritium breeding requirements. The sensitivity of tritium breeding to design and nuclear data parameters is reviewed. A framework for an integrated approach to improve tritium breeding prediction is discussed with emphasis on nuclear data requirements

  19. Dependency of irradiation damage density on tritium migration behaviors in Li2TiO3

    International Nuclear Information System (INIS)

    Kobayashi, Makoto; Toda, Kensuke; Oya, Yasuhisa; Okuno, Kenji

    2014-01-01

    Tritium migration behaviors in Li 2 TiO 3 with the increase of irradiation damage density were investigated by means of electron spin resonance and thermal desorption spectroscopy. The irradiation damages of F + -centers and O − -centers were formed by neutron irradiation, and their damage densities were increased with increasing neutron fluence. Tritium release temperature was clearly shifted toward higher temperature side with increasing neutron fluence, i.e. increasing damage density. The rate determining process for tritium release was also clearly changed depending on the damage density. Tritium release was mainly controlled by tritium diffusion process in crystalline grain of Li 2 TiO 3 at lower neutron fluence. The apparent tritium diffusivity was reduced as the damage density in Li 2 TiO 3 increased due to the introduction of tritium trapping/detrapping sites for diffusing tritium. Then, tritium trapping/detrapping processes began to control the overall tritium release with further damage introductions as the amount of tritium trapping sites increased enough to trap most of tritium in Li 2 TiO 3 . The effects of water vapor in purge gas on tritium release behaviors were also investigated. It was considered that hydrogen isotopes in purge gas would be dissociated and adsorbed on the surface of Li 2 TiO 3 . Then, hydrogen isotopes diffused inward Li 2 TiO 3 would occupy the tritium trapping sites before diffusing tritium reaches to these sites, promoting apparent tritium diffusion consequently. Kinetics analysis of tritium release for highly damaged Li 2 TiO 3 showed that the rate determining process of tritium release was the detrapping process of tritium formed as hydroxyl groups. The rate of tritium detrapping as hydroxyl groups was determined by the kinetic analysis, and was comparable to tritium release kinetics for Li 2 O, LiOH and Li 4 TiO 4 . The dangling oxygen atoms (O − -centers) formed by neutron irradiation would contribute strongly on the

  20. Tritium permeation through iron

    International Nuclear Information System (INIS)

    Hagi, Hideki; Hayashi, Yasunori

    1989-01-01

    An experimental method for measuring diffusion coefficients and permeation rates of tritium in metals around room temperature has been established, and their values in iron have been obtained by using the method. Permeation rates of tritium and hydrogen through iron were measured by the electrochemical method in which a tritiated aqueous solution was used as a cathodic electrolyte. Tritium and hydrogen were introduced from one side of a membrane specimen by cathodic polarization, while at the other side of the specimen the permeating tritium and hydrogen were extracted by potentiostatical ionization. The amount of permeated hydrogen was obtained by integrating the anodic current, and that of tritium was determined by measuring the radioactivity of the electrolyte sampled from the extraction side. Diffusion coefficients of tritium (D T ) and hydrogen (D H ) were determined from the time lag of tritium and hydrogen permeation. D T =9x10 -10 m 2 /s and D H =4x10 -9 m 2 /s at 286 K for annealed iron specimens. These values of D T and D H were compared with the previous data of the diffusion coefficients of hydrogen and deuterium, and the isotope effect in diffusion was discussed. (orig.)

  1. Tritium contamination experience in an operational D-T fusion reactor

    International Nuclear Information System (INIS)

    Gentile, C.A.; Ascione, G.

    1994-01-01

    During December 1993, the Tokamak Fusion Test Reactor (TFTR) injected a mixture of deuterium and tritium in the TFTR vacuum vessel for the purpose of creating D-T plasmas. The tritium used in these D-T plasmas was stored, delivered and processed in the TFTR tritium facility that includes the tritium vault, waste handling area, clean-up area, and gas holding tank room. During this time period, several components in the tritium process system were found to have tritium leaks which led to tritium deposition on process skids, components and floor area. Radiological surveys of surfaces contaminated with tritium oxide indicate a decrease in surface contamination in time (on the order of 12 to 36 hours) as the result of room ventilation. In instances where the facility HVAC system was maintained in the purge mode, a dramatic decrease in surface contamination was observed. Areas contaminated with tritium oxide (> 16.6 Bq/100 cm 2 ) were found to be clean ( 2 ) after several hours of continuous purging by the facility HVAC system. In instances where relative humidity was not decreased, the tritium surface contamination was found to be attenuated. During the months of December 1993, January and February 1994 tritium leaking components were either replaced, redesigned or repaired. During this time period, data were collected in the form of contamination surveys, real time tritium monitor output, and HVAC configuration indicating the correlation of purge ventilation leading to a decrease in tritium oxide surface contamination

  2. Tritium technology. A Canadian overview

    Energy Technology Data Exchange (ETDEWEB)

    Hemmings, R.L. [Canatom NPM (Canada)

    2002-10-01

    An overview of the various tritium research and operational activities in Canada is presented. These activities encompass tritium processing and recovery, tritium interactions with materials, and tritium health and safety. Many of these on-going activities form a sound basis for the tritium use and handling aspects of the ITER project. Tritium management within the CANDU heavy water reactor, associated detritiation facilities, research and development facilities, and commercial industry and improving the understanding of tritium behaviour in humans and the environment remain the focus of a long-standing Canadian interest in tritium. While there have been changes in the application of this knowledge and experience over time, the operating experience and the supporting research and development continue to provide for improved plant and facility operations, an improved understanding of tritium safety issues, and improved products and tools that facilitate tritium management. (author)

  3. Tritium technology. A Canadian overview

    International Nuclear Information System (INIS)

    Hemmings, R.L.

    2002-01-01

    An overview of the various tritium research and operational activities in Canada is presented. These activities encompass tritium processing and recovery, tritium interactions with materials, and tritium health and safety. Many of these on-going activities form a sound basis for the tritium use and handling aspects of the ITER project. Tritium management within the CANDU heavy water reactor, associated detritiation facilities, research and development facilities, and commercial industry and improving the understanding of tritium behaviour in humans and the environment remain the focus of a long-standing Canadian interest in tritium. While there have been changes in the application of this knowledge and experience over time, the operating experience and the supporting research and development continue to provide for improved plant and facility operations, an improved understanding of tritium safety issues, and improved products and tools that facilitate tritium management. (author)

  4. Tritium contamination of concrete walls and floors in tritium-handling laboratory

    International Nuclear Information System (INIS)

    Kawano, T.; Kuroyanagi, M.; Tabei, T.

    2006-01-01

    relation between surface contamination obtained with the smear method and inner contamination obtained with the direct-immersion method. The results revealed that surface contamination did not correspond to inner contamination. This means that contamination of the concrete walls and floors themselves cannot be evaluated from data on surface contamination. We also evaluated the dependence of tritium contamination in concrete walls and floors on depth. Maximum contamination was frequently found inside walls and floors. It could be inferred that tritium existed in the chemical form of hydrogen molecules (tritium gas) that crept into deeper locations within concrete walls or floors, changed its form to water through an isotope exchange reaction, and remained there. (authors)

  5. Tritium in the Savannah River Site environment

    Energy Technology Data Exchange (ETDEWEB)

    Murphy, C.E. Jr.; Bauer, L.R.; Hayes, D.W.; Marter, W.L.; Zeigler, C.C.; Stephenson, D.E.; Hoel, D.D.; Hamby, D.M.

    1991-05-01

    Tritium is released to the environment from many of the operations at the Savannah River Site. The releases from each facility to the atmosphere and to the soil and streams, both from normal operations and inadvertent releases, over the period of operation from the early 1950s through 1988 are presented. The fate of the tritium released is evaluated through environmental monitoring, special studies, and modeling. It is concluded that approximately 91% of the tritium remaining after decay is now in the oceans. A dose and risk assessment to the population around the site is presented. It is concluded that about 0.6 fatal cancers may be associated with the tritium released during all the years of operation to the population of about 625,000. This same population (based on the overall US cancer statistics) is expected to experience about 105,000 cancer fatalities from all types of cancer. Therefore, it is considered unlikely that a relationship between any of the cancer deaths occurring in this population and releases of tritium from the SRS will be found.

  6. Tritium in the Savannah River Site environment

    International Nuclear Information System (INIS)

    Murphy, C.E. Jr.; Bauer, L.R.; Hayes, D.W.; Marter, W.L.; Zeigler, C.C.; Stephenson, D.E.; Hoel, D.D.; Hamby, D.M.

    1991-05-01

    Tritium is released to the environment from many of the operations at the Savannah River Site. The releases from each facility to the atmosphere and to the soil and streams, both from normal operations and inadvertent releases, over the period of operation from the early 1950s through 1988 are presented. The fate of the tritium released is evaluated through environmental monitoring, special studies, and modeling. It is concluded that approximately 91% of the tritium remaining after decay is now in the oceans. A dose and risk assessment to the population around the site is presented. It is concluded that about 0.6 fatal cancers may be associated with the tritium released during all the years of operation to the population of about 625,000. This same population (based on the overall US cancer statistics) is expected to experience about 105,000 cancer fatalities from all types of cancer. Therefore, it is considered unlikely that a relationship between any of the cancer deaths occurring in this population and releases of tritium from the SRS will be found

  7. Scoping studies of tritium handling in a tokamak experimental power reactor

    International Nuclear Information System (INIS)

    Cherdack, R.; Watson, J.S.; Clinton, S.D.; Fisher, P.W.

    1975-01-01

    Tritium handling techniques in an experimental fusion power reactor (EPR) are evaluated to determine the requirements of the system and to compare different equipment and techniques for meeting those requirements. Tritium process equipment is needed to (1) evacuate and maintain a vacuum in the plasma vessel and the neutral beam injectors, (2) purify and recycle tritium and deuterium for the plasma fuel cycle, (3) recover tritium from experimental breeding modules, and (4) provide tritium containment and atmospheric cleanup. A development program is outlined to develop and demonstrate the required techniques and equipment and to permit confident design of an EPR for operation by the mid-1980s

  8. Relation between tritium concentration and chemical composition in rain at Fukuoka

    International Nuclear Information System (INIS)

    Hayashi, Y.; Momoshima, N.; Maeda, Y.; Kakiuchi, H.

    1999-01-01

    Tritium concentrations in rain collected at Fukuoka, Japan from 1982 have been measured. From May 1996 tritium concentrations and chemical species have been analyzed for each rain to examine their relationship. Recent rain was concluded not to be affected by tritium from atmospheric nuclear tests. Tritium concentrations showed a seasonal pattern, high during winter and spring and low during summer and fall and had positive correlations with non-sea-salt SO 4 2- , indicating a long distance of acidic materials as well as tritium from continental China. (author)

  9. Tritium forms discrimination in ryegrass under constant tritium exposure: From seed germination to seedling autotrophy.

    Science.gov (United States)

    Renard, H; Maro, D; Le Dizès, S; Escobar-Gutiérrez, A; Voiseux, C; Solier, L; Hébert, D; Rozet, M; Cossonnet, C; Barillot, R

    2017-10-01

    Uncertainties remain regarding the fate of atmospheric tritium after it has been assimilated in grasslands (ryegrass) in the form of TFWT (Tissue Free Water Tritium) or OBT (Organically Bound Tritium). One such uncertainty relates to the tritium forms discrimination during transfer from TFWT to OBT resulting from photosynthesis (OBT photo ), corresponding to the OBT photo /TFWT ratio. In this study, the OBT/TFWT ratio is determined by experiments in the laboratory using a ryegrass model and hydroponic cultures, with constant activity of tritium in the form of tritiated water (denoted as HTO) in the "water" compartment (liquid HTO) and "air" compartment (HTO vapour in the air). The OBT photo /TFWT ratio and the exchangeable OBT fraction are measured for three parts of the plant: the leaf, seed and root. Plant growth is modelled using dehydrated biomass measurements taken over time in the laboratory and integrating physiological functions of the plant during the first ten days after germination. The results suggest that there is no measurable discrimination of tritium in the plant organic matter produced by photosynthesis. Copyright © 2017 Elsevier Ltd. All rights reserved.

  10. Experience in handling concentrated tritium

    International Nuclear Information System (INIS)

    Holtslander, W.J.

    1985-12-01

    The notes describe the experience in handling concentrated tritium in the hydrogen form accumulated in the Chalk River Nuclear Laboratories Tritium Laboratory. The techniques of box operation, pumping systems, hydriding and dehydriding operations, and analysis of tritium are discussed. Information on the Chalk River Tritium Extraction Plant is included as a collection of reprints of papers presented at the Dayton Meeting on Tritium Technology, 1985 April 30 - May 2

  11. Problems of anthropogenic tritium limitation

    Directory of Open Access Journals (Sweden)

    Kochetkov О.A.

    2013-12-01

    Full Text Available This article contains the current situation in respect to the environmental concentrations of anthropogenic and natural tritium. There are presented and analyzed domestic standards for НТО of all Radiation Safety Standards (NRB, as well as the regulations analyzed for tritium in drinking water taken in other countries today. This article deals with the experience of limitation of tritium and focuses on the main problem of rationing of tritium — rationing of organically bound tritium.

  12. Trace Atmospheric Gas Analyzer (TAGA) Volatile Organic Compound (VOC) Data for BP Spill/Deepwater Horizon - June 2010

    Data.gov (United States)

    U.S. Environmental Protection Agency — The Trace Atmospheric Gas Analyzer (TAGA) buses are self-contained mobile laboratories that conduct instant-result monitoring of air quality at particular locations....

  13. Trace Atmospheric Gas Analyzer (TAGA) Volatile Organic Compound (VOC) Data for BP Spill/Deepwater Horizon - August 2010

    Data.gov (United States)

    U.S. Environmental Protection Agency — The Trace Atmospheric Gas Analyzer (TAGA) buses are self-contained mobile laboratories that conduct instant-result monitoring of air quality at particular locations....

  14. Trace Atmospheric Gas Analyzer (TAGA) Volatile Organic Compound (VOC) Data for BP Spill/Deepwater Horizon - July 2010

    Data.gov (United States)

    U.S. Environmental Protection Agency — The Trace Atmospheric Gas Analyzer (TAGA) buses are self-contained mobile laboratories that conduct instant-result monitoring of air quality at particular locations....

  15. Trace Atmospheric Gas Analyzer (TAGA) Volatile Organic Compound (VOC) Data for BP Spill/Deepwater Horizon - May 2010

    Data.gov (United States)

    U.S. Environmental Protection Agency — The Trace Atmospheric Gas Analyzer (TAGA) buses are self-contained mobile laboratories that conduct instant-result monitoring of air quality at particular locations....

  16. Process and device for stage by stage enrichment of deuterium and/or tritium in a material suitable for isotope exchange of deuterium and tritium with hydrogen

    International Nuclear Information System (INIS)

    Iniotakis, N.; Decken, C.B. von der.

    1983-01-01

    Water containing deuterium and/or tritium is first introduced into a carrier gas flow and reduced for the stage by stage enrichment of deuterium and/or tritium. A hydrogen partial pressure of a maximum of 100 millibar is set in the carrier gas flow. The carrier gas flow is taken along the primary side of an exchange wall suitable for the permeation of hydrogen, and a further carrier gas flow flows on its secondary side, which contains water or hydrogen. Reaction products formed after isotope exchange of deuterium and/or tritium with hydrogen are removed by the secondary carrier gas flow. (orig./HP) [de

  17. Effects of 108 Days Tritium Exposure on UHMW-PE, PTFE, and Vespel(R)

    International Nuclear Information System (INIS)

    Clark, E.A.

    2003-01-01

    Samples of three polymers, Ultra-High Molecular Weight Polyethylene (UHMW-PE), polytetrafluoroethylene (PTFE), also known as Teflon(R), and Vespel(R) polyimide were exposed to 1 atmosphere of tritium gas at ambient temperature for 108 days. Sample mass and size measurements to calculate density, spectra-colorimetry, dynamic mechanical analysis (DMA), and Fourier-transform infrared spectroscopy (FT-IR) were employed to characterize the effects of this exposure on these samples. This technical report is the first report from this research program

  18. Permeability of protective coatings to tritium

    International Nuclear Information System (INIS)

    Braun, J.M.

    1987-10-01

    The permeability of four protective coatings to tritium gas and tritiated water was investigated. The coatings, including two epoxies, one vinyl and one urethane, were selected for their suitability in CANDU plant service in Ontario Hydro. Sorption rates of tritium gas into the coatings were considerably larger than for tritiated water, by as much as three to four orders of magnitude. However, as a result of the very large solubility of tritiated water in the coatings, the overall permeability to tritium gas and tritiated water are comparable, being somewhat larger for HTO. Marked differences were also evident among the four coatings, the vinyl proving to be unique in behaviour and morphology. Because of a highly porous surface structure water condensation takes place at high relative humidities, leading to an abnormally high retention of free water. Desorption rates from the four coatings were otherwise quite similar. Of practical importance was the observation that more effective desorption of tritiated water could be carried out at relatively high humidities, in this case 60%. It was believed that isotopic exchange was responsible for this phenomenon. It appears that epoxy coatings having a high pigment-to-binder ratio are most suited for coating concrete in tritium handling facilities

  19. Tritium breeding and release-rate kinetics from neutron-irradiated lithium oxide

    International Nuclear Information System (INIS)

    Quanci, J.F.

    1989-01-01

    The research encompasses the measurement of the tritium breeding and release-rate kinetics from lithium oxide, a ceramic tritium-breeding material. A thermal extraction apparatus which allows the accurate measurement of the total tritium inventory and release rate from lithium oxide samples under different temperatures, pressures and carrier-gas compositions with an uncertainty not exceeding 3% was developed. The goal of the Lithium Blanket Module program was to determine if advanced computer codes could accurately predict the tritium production in the lithium oxide blanket of a fusion power plant. A fusion blanket module prototype was built and irradiated with a deuterium-tritium fusion-neutron source. The tritium production throughout the module was modeled with the MCNP three dimensional Monte Carlo code and was compared to the assay of the tritium bred in the module. The MCNP code accurately predicted tritium-breeding trends but underestimated the overall tritium breeding by 30%. The release rate of tritium from small grain polycrystalline sintered lithium oxides with a helium carrier gas from 300 to 450 C was found to be controlled by the first order surface desorption of monotritiated water. When small amounts of hydrogen were added to the helium carrier gas, the first order rate constant increased from the isotopic exchange of hydrogen for tritium at the lithium oxide surface occurring in parallel with the first order desorption process. The isotopic-exchange first order rate constant temperature dependence and hydrogen partial pressure dependence were evaluated

  20. Emissions of Monoxide of Carbon and Methane in an atmospheric burner of natural gas

    International Nuclear Information System (INIS)

    Amell A, A.A.; Gil B, E.; Cadavid S, F.J.

    1999-01-01

    In Colombia, the development of gas equipment industry has been characterized by a copy of foreign systems, without going further on the basic principles of operation and design of gas appliances. In order to guarantee an efficient and safe use of this energetic during the present plan of massive use of gas in the country, is necessary to know and dominate all the main phenomena influencing the design and operation of gas appliances, among them is the rate of primary aeration. In this study we analyze the production of CO and CH4 emissions in a premixed atmospheric burner when we modify pressure supply, tip size, injector size, mixer length and diameter of the throat. Results show that mixer geometry has a great influence on CO and CH4 emissions. When aeration rate was less or equal than 0.5 for power greater than 2.3 kw, CO emissions were beyond critic boundary. In the other hand, when we increased gas pressure supply, we observed those CH4 emissions decreased

  1. In situ measurement of tritium permeation through stainless steel

    Science.gov (United States)

    Luscher, Walter G.; Senor, David J.; Clayton, Kevin K.; Longhurst, Glen R.

    2013-06-01

    The TMIST-2 irradiation experiment was conducted in the Advanced Test Reactor at Idaho National Laboratory to evaluate tritium permeation through Type 316 stainless steel (316 SS). The interior of a 316 SS seamless tube specimen was exposed to a 4He carrier gas mixed with a specified quantity of tritium (T2) to yield partial pressures of 0.1, 5, and 50 Pa at 292 °C and 330 °C. In situ tritium permeation measurements were made by passing a He-Ne sweep gas over the outer surface of the specimen to carry the permeated tritium to a bubbler column for liquid scintillation counting. Results from in situ permeation measurements were compared with predictions based on an ex-reactor permeation correlation in the literature. In situ permeation data were also used to derive an in-reactor permeation correlation as a function of temperature and pressure over the ranges considered in this study. In addition, the triton recoil contribution to tritium permeation, which results from the transmutation of 3He to T, was also evaluated by introducing a 4He carrier gas mixed with 3He at a partial pressure of 1013 Pa at 330 °C. Less than 3% of the tritium resulting from 3He transmutation contributed to tritium permeation.

  2. Research of CITP-II tritium production irradiation device design

    International Nuclear Information System (INIS)

    Zhang Zhihua; Deng Yongjun; Mi Xiangmiao; Li Rundong; Liu Zhiyong

    2012-01-01

    As the core component of CITP-II, the online tritium production irradiation device is the pivotal equipment in the research on tritium production and release of tritium breeders. The design of CITP-II online tritium production irradiation device creatively makes replacing the breeders online come true; as tritium production capacity, the self-shielding factor of device, and neutron flux were studied. The influence of different load models and load thicknesses of breeders to tritium production capacity was calculated. The hydrodynamics parameters of device in solid-gas phase were computed. Thermal parameters, such as the heat power of breeders, hotspot, temperature grads distributions, utmost temperature, uneven factors, were analyzed. Creatively designed nonlinear electric heater equalized breeders' even heat power. The influence laws of the components, pressure of gap gas and carrier gas to the balance temperature were got. And the key thermal parameters were ascertained. The key thermal parameters and the changing laws were got and provide the basis for structural optimization and safety analysis. They can also be referenced for the study of breeders' tritium production and release. (authors)

  3. Continuous processing of polymers in repetitively pulsed atmospheric pressure discharges with moving surfaces and gas flow

    Energy Technology Data Exchange (ETDEWEB)

    Bhoj, Ananth N [Department of Chemical and Biomolecular Engineering, University of Illinois, Urbana, IL 61801 (United States); Kushner, Mark J [Department of Electrical and Computer Engineering, Iowa State University, Ames, IA 50011 (United States)

    2007-11-21

    Atmospheric pressure corona discharges are industrially employed to treat large areas of commodity polymer sheets by creating new surface functional groups. The most common processes use oxygen containing discharges to affix oxygen to hydrocarbon polymers, thereby increasing their surface energy and wettability. The process is typically continuous and is carried out in a web configuration with film speeds of tens to hundreds of cm s{sup -1}. The densities and relative abundances of functional groups depend on the gas composition, gas flow rate and residence time of the polymer in the discharge zone which ultimately determine the magnitude and mole fractions of reactive fluxes to the surface. In this paper, results are discussed from a two-dimensional computational investigation of the atmospheric pressure plasma functionalization of a moving polypropylene sheet in repetitively pulsed He/O{sub 2}/H{sub 2}O discharges. O and OH typically initiate surface processing by hydrogen abstraction. These species are regenerated during every plasma pulse but are also largely consumed during the inter-pulse period. Longer-lived species such as O{sub 3} accumulate over many pulses and convect downstream with the gas flow. Optimizing the interplay between local rapid reactions, such as H abstraction which occurs dominantly in the discharge zone, and non-local slower processes, such as surface-surface reactions, may enable the customization of the relative abundance of surface functional groups.

  4. Continuous processing of polymers in repetitively pulsed atmospheric pressure discharges with moving surfaces and gas flow

    International Nuclear Information System (INIS)

    Bhoj, Ananth N; Kushner, Mark J

    2007-01-01

    Atmospheric pressure corona discharges are industrially employed to treat large areas of commodity polymer sheets by creating new surface functional groups. The most common processes use oxygen containing discharges to affix oxygen to hydrocarbon polymers, thereby increasing their surface energy and wettability. The process is typically continuous and is carried out in a web configuration with film speeds of tens to hundreds of cm s -1 . The densities and relative abundances of functional groups depend on the gas composition, gas flow rate and residence time of the polymer in the discharge zone which ultimately determine the magnitude and mole fractions of reactive fluxes to the surface. In this paper, results are discussed from a two-dimensional computational investigation of the atmospheric pressure plasma functionalization of a moving polypropylene sheet in repetitively pulsed He/O 2 /H 2 O discharges. O and OH typically initiate surface processing by hydrogen abstraction. These species are regenerated during every plasma pulse but are also largely consumed during the inter-pulse period. Longer-lived species such as O 3 accumulate over many pulses and convect downstream with the gas flow. Optimizing the interplay between local rapid reactions, such as H abstraction which occurs dominantly in the discharge zone, and non-local slower processes, such as surface-surface reactions, may enable the customization of the relative abundance of surface functional groups

  5. Calibration of a Noble Gas Mass Spectrometer with an Atmospheric Argon Standard (Invited)

    Science.gov (United States)

    Prasad, V.; Grove, M.

    2009-12-01

    Like other mass spectrometers, gas source instruments are very good at precisely measuring isotopic ratios but need to be calibrated with a standard to be accurate. The need for calibration arises due to the complicated ionization process which inefficiently and differentially creates ions from the various isotopes that make up the elemental gas. Calibration of the ionization process requires materials with well understood isotopic compositions as standards. Our project goal was to calibrate a noble gas (Noblesse) mass spectrometer with a purified air sample. Our sample obtained from Ocean Beach in San Francisco was under known temperature, pressure, volume, humidity. We corrected the pressure for humidity and used the ideal gas law to calculate the number of moles of argon gas. We then removed all active gasses using specialized equipment designed for this purpose at the United States Geological Survey. At the same time, we measured the volume ratios of various parts of the gas extraction line system associated with the Noblesse mass spectrometer. Using this data, we calculated how much Ar was transferred to the reservoir from the vacuum-sealed vial that contained the purified gas standard. Using similar measurements, we also calculated how much Ar was introduced into the extraction line from a pipette system and how much of this Ar was ultimately expanded into the Noblesse mass spectrometer. Based upon this information, it was possible to calibrate the argon sensitivity of the mass spectrometer. From a knowledge of the isotopic composition of air, it was also possible to characterize how ionized argon isotopes were fractionated during analysis. By repeatedly analyzing our standard we measured a 40Ar Sensitivity of 2.05 amps/bar and a 40Ar/36Ar ratio of 309.2 on the Faraday detector. In contrast, measurements carried out by ion counting using electron multipliers yield a value (296.8) which is much closer to the actual atmospheric 40Ar/36Ar value of 295.5.

  6. Tritium waste control: April--September 1977

    International Nuclear Information System (INIS)

    1978-01-01

    A pilot scale system was used in an initial experiment to investigate the combined-electrolysis-catalytic-exchange process (CECE) for the detritiation of water. Data taken during the experiment indicate the process does indeed strip tritium from gaseous hydrogen at the top and concentrate it in water at the bottom of the catalyst-filled column. A high activity tritiated water electrolysis system was designed and built using a solid polymer electrolyte (SPE) cell. The system was successfully operated at currents up to 50 A using deionized tap water. Triplicate samples of cement, cement-plaster (1:1 ratio by weight), and cement-plaster (1:1 ratio by volume) were injected with 386 Ci of tritium. Preliminary results indicate Type III Portland cement retains the tritium slightly better than the cement-plaster mixtures. The tritium release study of actual waste burial packages is continuing. The fractional release is 1 x 10 -5 on a 4-y old package, only 4 x 10 -7 on 3-y old packages, and 1 x 10 -9 on a 1-y old package. Pressure increase and gas composition determinations were repeated for octane (activity = 1000 Ci/liter) with and without tritium fixation using argon as the initial overgas. Pressure buildup measurements for octane without fixation were repeated a third time using hydrogen gas. The rate of pressure increase did not change significantly from previously determined values. Four elemental tritium samples were released into a laboratory to determine the efficiency of the Emergency Containment System. The ventilation system was modified during the fourth experiment to minimize leakage

  7. Development of tritium cleanup system for LHD

    International Nuclear Information System (INIS)

    Sakuma, Yoichi; Kawano, Takao; Shibuya, Mamoru; Kabutomori, Toshiki

    2000-01-01

    Energy is vital for humans and we have been consuming a large amount of fossil fuel especially from the beginning of the industrial revolution. Nowadays its huge consumption has however come to threaten our life and we have to prepare nonfossil fuels, for instance solar energy, biomass energy, nuclear energy and so on. Fusion energy is an unlimited resource and one of the strongest candidates of the future energy source. At the National Institute for Fusion Science (referred to as 'NIFS' hereafter), we have constructed a new fusion experimental device called large helical device (referred to as 'LHD' hereafter) in 1998. The device will generate a small amount of tritium, as a fusion product. In order to remove it from the exhaust gas, we have designed a tritium cleanup system based on a new concept. This system is mainly composed of a palladium permeater, a decomposer and hydrogen absorbing alloys. It may perfectly recover the tritium from exhaust gas without oxidizing it. This system is applicable for the future needs at fusion power plants. In order to remove tritium discharged from fusion experimental facilities, it is usual to employ a system by which tritiated constituents, in various chemical forms, are entirely converted to a form of water vapor by catalytic oxidation. The water vapor containing tritiated form is then absorbed by molecular sieve (referred to as 'wet system' hereafter). However, in the case of LHD, it is not rational to deliberately convert the discharged tritium into the water vapor, because the tritium discharged from LHD is almost in a form of hydrogen molecules. Moreover, the tritium in the form of water vapor affects the human body 18000 times stronger than that of hydrogen molecules. In accordance with these view points, we have developed another type of tritium cleanup system based on a new concept, in which hydrogen molecules including tritiated ones (HT, DT and T 2 ) found in the exhaust gas of LHD are directly fixed to hydrogen

  8. Gaseous Tritium Light Sources in armament and watches industries

    International Nuclear Information System (INIS)

    Amme, Marcus; Siegenthaler, Roger

    2015-01-01

    The industrial application of Tritium gas enclosed in glass tubes is a modern way illuminating instruments and items wherever instant and independent readability is prerequisite. The GTLS (Gaseous Tritium Light Sources) technology follows the principle of radiation-induced luminescence and supersedes the luminous radioactive paints and their hazards such as particles erasure or heavy isotope use. Enclosure of tritium in glass is a demanding micro technology process and work needs to be performed in controlled areas due to handling of open sources. The storage and transport of the Tritium is done via licensed B(U)-containers coming from heavy water reactor sites, and disposal of radioactive Tritium wastes has to be compliant with national and international regulations for transport and waste management.

  9. The tritium systems test assembly: Overview and recent results

    International Nuclear Information System (INIS)

    Bartlit, J.R.; Anderson, J.L.

    1988-01-01

    The fusion technology development program for tritium in the US is centered around the Tritium Systems Test Assembly (TSTA) at Los Alamos National Laboratory. The TSTA is a full-scale system of reactor exhaust gas reprocessing for an ITER-sized machine. That is, TSTA has the capacity to process tritium in a closed loop mode at the rate of 1 kg per day, requiring a tritium inventory of about 100 g. The TSTA program also interacts with all other tritium-related fusion technology programs in the US and all major programs abroad. This report summarizes the current status, results and interactions of the TSTA. Special emphasis is given to operations in May/June using large compound cryopumps that completed the fuel loop integration of all TSTA subsystems for the first time. 6 refs., 2 figs

  10. Tritium isotope fractionation in biological systems and in analytical procedures

    International Nuclear Information System (INIS)

    Kim, M.A.; Baumgaertner, Franz

    1989-01-01

    The organically bound tritium (OBT) is evaluated in biological systems by determining the tritium distribution ratio (R-value), i.e. tritium concentrations in organic substance to cell water. The determination of the R-value always involves isotope fractionation is applied analytical procedures and hence the evaluation of the true OBT -value in a given biological system appears more complicated than hitherto known in the literature. The present work concentrates on the tritium isotope fractionation in the cell water separation and on the resulting effects on the R-value. The analytical procedures examined are vacuum freeze drying under equilibrium and non-equilibrium conditions and azeotropic distillation. The vaporization isotope effects are determined separately in the phase transition of solid or liquid to gas in pure tritium water systems as well as in real biological systems, e.g. corn plant. The results are systematically analyzed and the influence of isotope effects on the R-value is rigorously quantified

  11. Tritium permeation and recovery

    International Nuclear Information System (INIS)

    Bond, R.A.; Hamilton, A.M.

    1987-01-01

    The paper is an appendix to a study of the reactor relevance of the NET design concept. The latter study examines whether the technologies and design principles proposed for NET can be directly extrapolated to a demonstration (DEMO) reactor. In this appendix, tritium transport in the DEMO breeding blanket is considered with emphasis on the permeation rate from the lithium-lead breeder into the coolant. A computational model used to calculate the tritium transport in the breeder blanket is described. Results are reported for the tritium transport in the NET/INTOR type blanket as well as the DEMO blanket in order to provide a comparison. In addition, results are presented for the helium coolant tritium extraction analysis. (U.K.)

  12. Tritium protective clothing

    International Nuclear Information System (INIS)

    Fuller, T.P.; Easterly, C.E.

    1979-06-01

    Occupational exposures to radiation from tritium received at present nuclear facilities and potential exposures at future fusion reactor facilities demonstrate the need for improved protective clothing. Important areas relating to increased protection factors of tritium protective ventilation suits are discussed. These areas include permeation processes of tritium through materials, various tests of film permeability, selection and availability of suit materials, suit designs, and administrative procedures. The phenomenological nature of film permeability calls for more standardized and universal test methods, which would increase the amount of directly useful information on impermeable materials. Improvements in suit designs could be expedited and better communicated to the health physics community by centralizing devlopmental equipment, manpower, and expertise in the field of tritium protection to one or two authoritative institutions

  13. Tritium breeding blanket

    International Nuclear Information System (INIS)

    Smith, D.; Billone, M.; Gohar, Y.; Baker, C.; Mori, S.; Kuroda, T.; Maki, K.; Takatsu, H.; Yoshida, H.; Raffray, A.; Sviatoslavsky, I.; Simbolotti, G.; Shatalov, G.

    1991-01-01

    The terms of reference for ITER provide for incorporation of a tritium breeding blanket with a breeding ratio as close to unity as practical. A breeding blanket is required to assure an adequate supply of tritium to meet the program objectives. Based on specified design criteria, a ceramic breeder concept with water coolant and an austenitic steel structure has been selected as the first option and lithium-lead blanket concept has been chosen as an alternate option. The first wall, blanket, and shield are integrated into a single unit with separate cooling systems. The design makes extensive use of beryllium to enhance the tritium breeding ratio. The design goals with a tritium breeding ratio of 0.8--0.9 have been achieved and the R ampersand D requirements to qualify the design have been identified. 4 refs., 8 figs., 2 tabs

  14. Tritium in plants

    International Nuclear Information System (INIS)

    Vichot, L.; Losset, Y.

    2009-01-01

    The presence of tritium in the environment stems from its natural production by cosmic rays, from the fallout of the nuclear weapon tests between 1953 and 1964, and locally from nuclear industry activities. A part of the tritiated water contained in the foliage of plants is turned into organically bound tritium (OBT) by photosynthesis. The tritium of OBT, that is not exchangeable and then piles up in the plant, can be used as a marker of the past. It has been shown that the quantity of OBT contained in the age-rings of an oak that grew near the CEA center of Valduc was directly correlated with the tritium releases of the center. (A.C.)

  15. Tritium-v. 2

    International Nuclear Information System (INIS)

    1987-01-01

    Several bibliographical references about tritium are shown. The following aspects are presented: properties, analysis, monitoring, dosimetry reactions, labelling, industrial production, radiological protection, applications to science, technology and industry and some processes to obtain the element. (E.G.) [pt

  16. Tritium protective clothing

    Energy Technology Data Exchange (ETDEWEB)

    Fuller, T. P.; Easterly, C. E.

    1979-06-01

    Occupational exposures to radiation from tritium received at present nuclear facilities and potential exposures at future fusion reactor facilities demonstrate the need for improved protective clothing. Important areas relating to increased protection factors of tritium protective ventilation suits are discussed. These areas include permeation processes of tritium through materials, various tests of film permeability, selection and availability of suit materials, suit designs, and administrative procedures. The phenomenological nature of film permeability calls for more standardized and universal test methods, which would increase the amount of directly useful information on impermeable materials. Improvements in suit designs could be expedited and better communicated to the health physics community by centralizing devlopmental equipment, manpower, and expertise in the field of tritium protection to one or two authoritative institutions.

  17. Establishment of tritium dating facility for hydrological studies in PNRI

    International Nuclear Information System (INIS)

    Mendoza, Norman; Sucgang, Raymond; Castaneda, Soledad

    2009-01-01

    The release of excess tritium ( 3 H) into the atmosphere from nuclear weapons tests conducted between 1952 and 1963 'tagged' rain water, and thereby all surface waters with 3 HHO. Measurement of 3 H concentrations in rain, surface water and groundwater is useful index of vulnerability and sustainability of the aquifer to pollution and human exploitation. These determinations are currently being used in the characterization of different environments and in pollution studies, in the framework of research projects, international collaborations and services. Liquid scintillation counting (LSC) was the method of choice for the evaluation of the tritium concentrations in precipitation, groundwater and surface water samples. Prior to counting process, the samples are enriched in tritium by an electrolysis procedure to improve the overall detection limit. Low-level hydrological water samples go through an electrolytic enrichment step, in which tritium concentrations are increased to about seventy-fold through volume reduction. The amount of tritium in water is expressed in tritium units (TU). Water samples taken from selected areas of Bulacan province within the period of 2007 and 2008 were analyzed as part of the current hydrological studies being done by our group in PNRI. The typical tritium values for the rain water, surface water, and groundwater were found to be 1.20±0.11 TU, 1.12±0.11 TU, and 0.40±0.07, respectively. Procedures are now available in our laboratory for measurement of tritium in water samples of different water types. (author)

  18. Retrospective evaluation of tritium fallout by tree-ring analysis

    International Nuclear Information System (INIS)

    Kozak, K.; Biro, T.; Golder, F.; Rank, D.; Rajner, V.; Staudner, F.

    1993-01-01

    Tritium analyses of tree-ring cellulose were made to test its suitability for retrospective evaluation of a local tritium fallout. Several spruce trees were taken from an Austrian alpine area where tritium contamination of May 1974 precipitation had been detected. Wood from the annual growth rings of 1973, 1974 and 1975 was separated and the cellulose extracted. After isotopic equilibration with dead water, cellulose was combusted to yield water, whose tritium concentration was measured by liquid scintillation counting. Rigorous statistical treatment proved the significance of the increased tritium concentration caused by the tritium anomaly, which occurred during the growing season. The long-term trends of local atmospheric tritium, including the 1974 peak, were also well reflected by analysis of a 24-year ring sequence from a single tree in the contaminated area. The tritium data gained by the given method can be used at present qualitatively and a better understanding of the possible sources of contamination is required in order that the quantitative criteria be satisfied. (Author)

  19. Chemical form of tritium released from solid breeder materials and the influences of it on a bred tritium recovery systems

    International Nuclear Information System (INIS)

    Furukubo, Y.; Nishikawa, M.; Nishida, Y.; Kinjyo, T.; Tanifuji, Takaaki; Kawamura, Yoshinori; Enoeda, Mikio

    2004-01-01

    The ratio of HTO in total tritium was measured at release of the bred tritium to the purge gas with hydrogen using the thermal release after irradiation method, where neutron irradiation was performed at JRR-3 reactor in JAERI or KUR reactor in Kyoto University. It is experimentally confirmed in this study that not a small portion of bred tritium is released to the purge gas in the form of HTO form ceramic breeder materials even when hydrogen is added to the purge gas. The chemical composition is to be decided by the competitive reaction at the grain surface of a ceramic breeder material where desorption reaction, isotope exchange reaction 1, isotope exchange reaction 2 and water formation reaction are considered to take part. Observation in this study implies that it is necessary to have a bred tritium recovery system applicable for both HT and HTO form to recover whole bred tritium. The chemical composition also decides the amount of tritium transferable to the cooling water of the electricity generation system through the structural material in the blanket system. Permeation behavior of tritium through some structural materials at various conditions are also discussed. (author)

  20. Gas Diffusion Barriers Prepared by Spatial Atmospheric Pressure Plasma Enhanced ALD.

    Science.gov (United States)

    Hoffmann, Lukas; Theirich, Detlef; Pack, Sven; Kocak, Firat; Schlamm, Daniel; Hasselmann, Tim; Fahl, Henry; Räupke, André; Gargouri, Hassan; Riedl, Thomas

    2017-02-01

    In this work, we report on aluminum oxide (Al 2 O 3 ) gas permeation barriers prepared by spatial ALD (SALD) at atmospheric pressure. We compare the growth characteristics and layer properties using trimethylaluminum (TMA) in combination with an Ar/O 2 remote atmospheric pressure plasma for different substrate velocities and different temperatures. The resulting Al 2 O 3 films show ultralow water vapor transmission rates (WVTR) on the order of 10 -6 gm -2 d -1 . In notable contrast, plasma based layers already show good barrier properties at low deposition temperatures (75 °C), while water based processes require a growth temperature above 100 °C to achieve equally low WVTRs. The activation energy for the water permeation mechanism was determined to be 62 kJ/mol.