Detection of helium-containing paramagnetic complex at decay of tritium incorporated in HTO and DTO

International Nuclear Information System (INIS)

Legasov, V.A.; Usatyj, A.F.; Ibragimov, R.A.; Myasoedov, N.F.

1979-01-01

EPR technique was used to study the paramagnetic centers appearing during long-term storage of frozen (77 K) non-deoxygenated light (H 2 O) and heavy (D 2 O) water containing 3.5% vol. highly active HTO (29 ci/cm 3 ), so that the resulting activity of the sample (0.1 ml) was about 100 mci. For comparison, the same samples containing no HTO but irradiated by Co-60 rays were studied under identical conditions. A schematic of the processes involved in tritium decay in DTO (or HTO) in the aqueous matrix frozen at low temperatures was suggested

Results of preliminary experiments on tritium decontamination by UV irradiation

International Nuclear Information System (INIS)

Oya, Yasuhisa; Shu, Wataru; O'hira, Shigeru; Hayashi, Takumi; Nishi, Masataka

2000-03-01

In the point of view of protection of workers from the radiation exposure and the limitation of the contamination with radioactive materials, it is important to decontaminate mobile tritium from plasma facing components of a nuclear fusion reactor at the beginning of their maintenance work. It is considered that the heating is the most effective method for decontamination. However, it is important to develop new decontamination method of adsorbed hydro-carbon based substances from the materials that cannot be heated or the inner pipe of double pipes. This report presents results of preliminary experiments performed for the development of the effective tritium decontamination technique pursuing under US/Japan collaborative program on technology for fusion-fuel processing (Annex IV). In the experiments, the effects of Ultra Violet (UV) irradiation on tritium removal from some kinds of materials, such as poly vinyl chloride -(CH 2 CHCl) n - film, polyethylene film and graphite samples coated by C 2 H 2 plasma were examined. As the result of UV irradiation, it was confined that hydrogen and carbon based compounds could be released from the specimen during UV irradiation. It is concluded that UV irradiation is one of the hopeful candidates for effective tritium decontamination. (author)

Experiment to study the β-decay of free atomic and molecular tritium

International Nuclear Information System (INIS)

Robertson, R.G.H.; Bowles, T.J.; Maley, M.; Browne, J.C.; Burritt, T.; Toevs, J.; Stelts, M.; Helfrick, J.; Knapp, D.; Ledebuhr, A.G.

1982-01-01

An apparatus is described which will allow the measurement of the β-decay of free tritium atoms and molecules for determining antineutrino mass. It consists of an RF dissociator, a long cylindrical decay region open at both ends, a guide field, and a magnetic spectrometer

Method and device for secure, high-density tritium bonded with carbon

Science.gov (United States)

Wertsching, Alan Kevin; Trantor, Troy Joseph; Ebner, Matthias Anthony; Norby, Brad Curtis

2016-04-05

A method and device for producing secure, high-density tritium bonded with carbon. A substrate comprising carbon is provided. A precursor is intercalated between carbon in the substrate. The precursor intercalated in the substrate is irradiated until at least a portion of the precursor, preferably a majority of the precursor, is transmutated into tritium and bonds with carbon of the substrate forming bonded tritium. The resulting bonded tritium, tritium bonded with carbon, produces electrons via beta decay. The substrate is preferably a substrate from the list of substrates consisting of highly-ordered pyrolytic graphite, carbon fibers, carbon nanotunes, buckministerfullerenes, and combinations thereof. The precursor is preferably boron-10, more preferably lithium-6. Preferably, thermal neutrons are used to irradiate the precursor. The resulting bonded tritium is preferably used to generate electricity either directly or indirectly.

Present status of irradiation tests on tritium breeding blanket for fusion reactor

International Nuclear Information System (INIS)

Futamura, Yoshiaki; Sagawa, Hisashi; Shimakawa, Satoshi; Tsuchiya, Kunihiko; Kuroda, Toshimasa; Kawamura, Hiroshi.

1994-01-01

To develop a tritium breeding blanket for a fusion reactor, irradiation tests in fission reactors are indispensable for obtaining data on irradiation effects on materials, and neutronics/thermal characteristics and tritium production/recovery performance of the blanket. Various irradiation tests have been conducted in the world, especially to investigate tritium release characteristics from tritium breeding and neutron multiplier materials, and materials integrity under irradiation. In Japan, VOM experiments at JRR-2 for ceramic breeders and experiments at JMTR for ceramic breeders and beryllium as a neutron multiplier have been performed. Several universities have also investigated ceramic breeders. In the EC, the EXOTIC experiments at HFR in the Netherlands and the SIBELIUS, the LILA, the LISA and the MOZART experiments for ceramic breeders have carried out. In Canada, NRU has been used for the CRITIC experiments. The TRIO experiments at ORR(ORNL), experiments at RTNS-II, FUBR and ATR have been conducted in the USA. The last two are experiments with high neutron fluence aiming at investigating materials integrity under irradiation. The BEATRIX-I and -II experiments have proceeded under international collaboration of Japan, Canada, the EC and the USA. This report shows the present status of these irradiation tests following a review of the blanket design in the ITER CDA(Conceptual Design Activity). (author)

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

Tritium release from neutron-irradiated Li2O: Transport in porous sintered pellets

International Nuclear Information System (INIS)

Tanifuji, Takaaki; Yamaki, Daiju; Jitsukawa, Shiro

2006-01-01

The tritium release behavior from Li 2 O sintered pellets (81-88% T.D.) is examined by isothermal heating tests. (1) For the 88% T.D. specimens, the fraction of residual tritium is found to follow the square-root law of the annealing time. The rate-determining process is the migration in the connected micro-pore. (2) For the 81% T.D. specimens, which are annealed after irradiation at 630 K for 4 h, the fraction of residual tritium is also found to follow the square-root law of the annealing time. The rate-determining process is the migration in the connected micro-pore. (3) For the 81% T.D. specimens as irradiated, the tritium release rate is found to follow the square-root law of the annealing time. The rate-determining process is controlled by Kohlrauch stretched exponential form. Tritium trapped in irradiation defects released with recovering the defects by isothermal heating

Determination of tritium generation and release parameters at lithium CPS under neutron irradiation

Energy Technology Data Exchange (ETDEWEB)

Ponkratov, Yuriy, E-mail: ponkratov@nnc.kz [Institute of Atomic Energy, National Nuclear Center of RK, Kurchatov (Kazakhstan); Baklanov, Viktor; Skakov, Mazhyn; Kulsartov, Timur; Tazhibayeva, Irina; Gordienko, Yuriy; Zaurbekova, Zhanna; Tulubayev, Yevgeniy [Institute of Atomic Energy, National Nuclear Center of RK, Kurchatov (Kazakhstan); Chikhray, Yevgeniy [Institute of Experimental and Theoretical Physics of Kazakh National University, Almaty (Kazakhstan); Lyublinski, Igor [JSC “Star”, Moscow (Russian Federation); NRNU “MEPhI”, Moscow (Russian Federation); Vertkov, Alexey [JSC “Star”, Moscow (Russian Federation)

2016-11-01

Highlights: • The main parameters of tritium generation and release from lithium capillary-porous system (CPS) under neutron irradiation at the IVG.1 M research reactor is described in paper. • In the experiments a very small tritium release was fixed likely due to its high solubility in liquid lithium. • If the lithium CPS will be used as a plasma facing material in temperature range up to 773 K under neutron irradiation only helium will release from lithium CPS into a vacuum chamber. - Abstract: This paper describes the main parameters of tritium generation and release from lithium capillary-porous system (CPS) under neutron irradiation at the IVG.1 M research reactor. The experiments were carried out using the method of mass-spectrometric registration of released gases and using a specially constructed ampoule device. Irradiation was carried out at different reactor thermal powers (1, 2 and 6 MW) and sample temperatures from 473 to 773 K. In the experiments a very small tritium release was detected likely due to its high solubility in liquid lithium. It can be caused by formation of lithium tritide during tritium diffusion to the lithium surface.

2017 Status report-Tritium aging studies on stainless steel: Effect of hydrogen, tritium and decay helium on the fracture-toughness properties of stem, cup and block forgings

Energy Technology Data Exchange (ETDEWEB)

Morgan, Michael J. [Savannah River Site (SRS), Aiken, SC (United States). Savannah River National Lab. (SRNL)

2017-06-28

The materials of construction of tritium reservoirs are forged stainless steels. During service, the structural properties of the stainless steel change over time because of the diffusion of tritium into the reservoir wall and its radioactive decay to helium-3. This aging effect can cause cracks to initiate and grow which could result in a tritium leak or delayed failure of a tritium reservoir. Numerous factors affect the tendency for crack formation and propagation and are being investigated in this program. The goal of the research is to provide relevant fracture mechanics data that can be used by the design agencies in their assessments of tritium reservoir structural integrity. In this status report, new experimental results are presented on the effects of tritium and decay helium on the cracking properties of specimens taken from actual tritium reservoir forgings instead of the experimental forgings of past programs. The properties measured are more representative of actual reservoir properties because the microstructure of the specimens tested are more like that of the actual tritium reservoirs. The program was designed to measure the effects of material variables on tritium compatibility and includes two stainless steels (Type 304L and 316L stainless steel), multiple yield strengths (360-500 MPa), and multiple forging shapes (Stem, Cup, and Block).

Progress report on the Los Alamos tritium beta decay experiment

International Nuclear Information System (INIS)

Wilkerson, J.F.; Bowles, T.J.; Knapp, D.A.; Robertson, R.G.H.; Wark, D.L.

1988-01-01

Measurements near the endpoint of the tritium beta-decay spectrum using a gaseous molecular tritium source yield an essentially model-independent upper limit of 27 eV on the /ovr ν//sub e/ mass at the 95% confidence level. Since demonstrating from this initial measurement the successful operation of a gaseous source based system, most of our effort has been concentrated towards the upgrade and optimization of the experimental apparatus. The emphasis of this work has been to eliminate or further reduce effects that generate systematic errors. Based on realistic projections from our initial measurement, an ultimate sensitivity to neutrino mass of 10 eV is expected. 12 refs., 1 fig

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}.

Determination of effective cross sections and production rates for tritium in the irradiation experiment TRIDEX

International Nuclear Information System (INIS)

Weise, L.

1986-04-01

In the framework of the development of a fusion reactor blanket the irradiation experiment TRIDEX (Tritium Recovery Irradiation DIDO Experiment) takes place at the Juelich Research Reactor FRJ-2 (DIDO). For this equipment the required neutronic calculations have been performed. The aim was the determination of the neutron spectrum and several therefrom derived integral parameters for the irradiation positions in interest. From the calculated effective cross sections for the formation of Tritium resulting from irradiated Lithium samples on one hand and from measured neutron flux densities on the other hand, all needed quantities of the Tritium production could be determined. The calculation of the neutron spectrum has been performed in a two-dimensional x-y-geometry. The neutron flux densities have been gained by gamma-spectrometric measurement of the activities in irradiated activation samples. (orig.) [de

Tritium release and retention properties of highly neutron-irradiated beryllium pebbles from HIDOBE-01 experiment

Energy Technology Data Exchange (ETDEWEB)

Chakin, V., E-mail: vladimir.chakin@kit.edu [Karlsruhe Institute of Technology, Institute for Applied Materials, Hermann-von-Helmholtz-Platz 1, 76344 Eggenstein-Leopoldshafen (Germany); Rolli, R.; Moeslang, A.; Klimenkov, M.; Kolb, M.; Vladimirov, P.; Kurinskiy, P.; Schneider, H.-C. [Karlsruhe Institute of Technology, Institute for Applied Materials, Hermann-von-Helmholtz-Platz 1, 76344 Eggenstein-Leopoldshafen (Germany); Til, S. van; Magielsen, A.J. [Nuclear Research and Consultancy Group, Westerduinweg 3, Postbus 25, 1755 ZG Petten (Netherlands); Zmitko, M. [The European Joint Undertaking for ITER and the Development of Fusion Energy, c/Josep Pla, no. 2, Torres Diagonal Litoral, Edificio B3, 08019 Barcelona (Spain)

2013-11-15

The current helium cooled pebble bed (HCPB) tritium breeding blanket concept for fusion reactors includes a bed of 1 mm diameter beryllium pebbles to act as a neutron multiplier. Beryllium pebbles, fabricated by the rotating electrode method, were neutron irradiated in the HFR in Petten within the HIDOBE-01 experiment. This study presents tritium release and retention properties and data on microstructure evolution of beryllium pebbles irradiated at 630, 740, 873, 948 K up to a damage dose of 18 dpa, corresponding to a helium accumulation of about 3000 appm. The measured cumulative released activity from the beryllium pebbles irradiated at 948 K was found to be significantly lower than the calculated value. After irradiation at 873 and 948 K scanning electron microscopy (SEM) and transmission electron microscopy (TEM) analyses revealed large pores or bubbles in the bulk and oxide films with a thickness of up to 8 μm at the surface of the beryllium pebbles. The radiation-enhanced diffusion of tritium and the formation of open porosity networks accelerate the tritium release from the beryllium pebbles during the high-flux neutron irradiation.

Comparison of the tritium residence times of various ceramic breeder materials irradiated in EXOTIC experiments 4 and 5

International Nuclear Information System (INIS)

Kwast, H.; Elen, J.D.; Conrad, R.; Casadio, S.; Werle, H.; Verstappen, G.

1990-09-01

Tritium residence times have been determined for various ceramic tritium breeding materials from in-situ release measurements. The irradiations, codenamed EXOTIC (EXtraction Of Tritium In Ceramics), were carried out in the High Flux Reactor (HFR) Petten. During the irradiation more than 450 transients were performed and the corresponding tritium release measured. Materials supplied by SCK/CEN (Li 2 ZrO 3 ), CEA (Li 2 ZrO 3 and LiAlO 2 ), ENEA (LiAlO 2 ), KfK (Li 4 SiO 4 ), NRL (Li 6 Zr 2 O 7 ) and ECN (Li 8 ZrO 6 ) were irradiated in EXOTIC-5 to compare the tritium residence times obtained under equal conditions. Apart from differences in density, grain size, pore size and OPV it appeared that the tritium residence times of the lithium zirconates (pellets) were shorter than those of the Li 4 SiO 4 pebbles. The tritium residence times of the Li 4 SiO 4 pebbles were shorter than those of the LiAlO 2 pellets. (author). 7 refs.; 5 figs.; 3 tabs

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

Tritium extraction mechanisms from lithium aluminates during in pile irradiation experiments

International Nuclear Information System (INIS)

Briec, M.; Roth, E.

1987-04-01

The principal aim was to determine ranges of parameters governing tritium release from γ lithium aluminates within which acceptable rates for their contemplated usage as tritium breeder material in a fusion reactor blanket could be obtained. in the first place values of every quantity involved should be known as well as possible. Reproducible results should be a criterium of validity of the selected parameters. It is shown from a description of a series of experiments that processes limiting tritium release rates are not the same in different temperature ranges. By varying the composition of purge gases used for tritium extraction, the level of irradiation fluxes, and by studying simultaneously samples of different textures, results were obtained and an assignment of the respective role of defect formation, texture, surface effect is attempted to interpret them

Theoretical investigation of the β decay of a negative tritium ion

International Nuclear Information System (INIS)

Goryaev, F.F.; Sukhanov, L.P.

1997-01-01

Calculation of probability of the main channel β decay of tritium negative ion as one of the possible process influencing the β spectrum form is carried out. The corresponding energy characteristics are estimated. The necessity of accounting for the investigated process by interpretation of the β spectrum experimental curves near the end point in connection with the problem of determining the neutrino rest mass, is pointed out

In-situ tritium recovery from Li2O irradiated in fast neutron flux - Beatrix-II temperature change specimen

International Nuclear Information System (INIS)

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

1992-01-01

The Beatrix-II irradiation experiment is an in-situ tritium release experiment to evaluate the stability and tritium release characteristics of Li 2 O under fast neutron irradiation to extended burnups. A thin annular ring specimen capable of temperature changes was irradiated in Phase I of the experiment to a lithium burnup of 5%. The primary emphasis of the test plan was to determine the effect and interrelationship of gas composition and temperature on the tritium inventory with increasing temperature and a series of specific temperature changes were carried out at intervals throughout the experiment to characterize the effect of burnup. Decreasing the amount of hydrogen in the sweep gas resulted in an increase in the tritium inventory in the Li 2 O specimen. The tritium recovery during startup and shutdown was observed to be strongly influenced by the composition of the sweep gas

Initial decay process of radicals induced in irradiated food

International Nuclear Information System (INIS)

Kaimori, Yoshihiko; Sakamoto, Yuki; Nakamura, Hideo; Ukai, Mitsuko; Kikuchi, Masahiro; Shimoyama, Yuhei; Kobayashi, Yasuhiko; Kameya, Hiromi

2011-01-01

In order to determine radial decay behaviors of γ-irradiated food, we analyzed radicals in the food using ESR. We detected the ESR signal of specimens just several minutes after irradiation. The singlet signal intensity at g=2.0, originated from organic free radicals was increased as followed by the increasing radiation dose. Singlet signal intensity that increased by γ-irradiation was decreased with time. The phenomena of decay of the ESR singlet signal showed two phase that are rapid decay and slow decay. It was suggested that those two phase decay is due to at least the two radical species. Also we concluded that after three hours of radiation treatment long life radical as ESR signal intensity was detected in irradiated specimen; black pepper, green coffee bean and ginseng, showed the same decay phenomena. But the signal intensity of irradiated black pepper was three times larger than that of irradiated green coffee bean and irradiated ginseng. (author)

Activation analysis of tritium breeder lithium lead irradiated by fusion neutrons in FDS-II

International Nuclear Information System (INIS)

Mingliang Chen

2006-01-01

R-and-D of fusion materials, especially their activation characteristics, is one of the key issues for fusion research in the world. Research on activation characteristics for low activation materials, such as reduced activation ferritic/martensitic steels, vanadium alloys and SiCf/SiC composites, is being done throughout the world to ensure the attractiveness of fusion power regarding safety and environmental aspects. However, there is less research on the activation characteristics of the other important fusion materials, such as tritium breeder etc.. Lithium lead (Li 17 Pb 83 ) is presently considered as a primary candidate tritium breeder for fusion power reactors because of its attractive characteristics. It can serve as a tritium breeder, neutron multiplier and coolant in the blanket at the same time. The radioactivity of Li 17 Pb 83 by D-T fusion neutrons in FDS-II has been calculated and analyzed. FDS-II is a concept design of fusion power reactor, which consists of fusion core with advanced plasma parameters extrapolated from the ITER (International Thermonuclear Experimental Reactor) and two candidates of liquid lithium breeder blankets (named SLL and DLL blankets). The neutron transport and activation calculation are carried out based on the one-dimensional model for FDS-II with the home-developed multi-functional code system VisualBUS and the multi-group data library HENDL1.0/MG and European Activation File EAF-99. The effects of irradiation time on the activation characteristics of Li 17 Pb 83 were analyzed and it concludes that the irradiation time has an important effect on the activation level of Li 17 Pb 83 . Furthermore, the results were compared with the activation levels of other tritium breeders, such as Li 4 SiO 4 , Li 2 TiO 3 , Li 2 O and Li etc., under the same irradiation conditions. The dominant nuclides to dose rate and activity of Li 17 Pb 83 were analyzed as well. Tritium generated by Li has a great contribution to the afterheat and

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 oxide with a helium carrier gas from 300 to 450 C was found to be controlled by the first order surface desorption of mono-tritiated 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. Large single crystals of lithium oxide were fabricated by the vacuum fusion technique. The release rate of tritium from the large single crystals was found to be controlled by diffusion, and the mixed diffusion-desorption controlled release regime

Tritium release kinetics in lithium orthosilicate ceramic pebbles irradiated with low thermal-neutron fluence

International Nuclear Information System (INIS)

Xiao, Chengjian; Gao, Xiaoling; Kobayashi, Makoto; Kawasaki, Kiyotaka; Uchimura, Hiromichi; Toda, Kensuke; Kang, Chunmei; Chen, Xiaojun; Wang, Heyi; Peng, Shuming; Wang, Xiaolin; Oya, Yasuhisa; Okuno, Kenji

2013-01-01

Tritium release kinetics in lithium orthosilicate (Li 4 SiO 4 ) ceramic pebbles irradiated with low thermal-neutron fluence was studied by out-of-pile annealing experiments. It was found that the tritium produced in Li 4 SiO 4 pebbles was mainly released as tritiated water vapor (HTO). The apparent desorption activation energy of tritium on the pebble surface was consistent with the diffusion activation energy of tritium in the crystal grains, indicating that tritium release was mainly controlled by diffusion process. The diffusion coefficients of tritium in the crystal grains at temperatures ranging from 450 K to 600 K were obtained by isothermal annealing tests, and the Arrhenius relation was determined to be D = 1 × 10 −7.0 exp (−40.3 × 10 3 /RT) cm 2 s −1

Tritium release kinetics in lithium orthosilicate ceramic pebbles irradiated with low thermal-neutron fluence

Energy Technology Data Exchange (ETDEWEB)

Xiao, Chengjian; Gao, Xiaoling [Institute of Nuclear Physics and Chemistry, China Academy of Engineering Physics, Box 919-214, Mian Yang 621900 (China); Kobayashi, Makoto; Kawasaki, Kiyotaka; Uchimura, Hiromichi; Toda, Kensuke [China Academy of Engineering Physics, Box 919-1, Mian Yang 621900 (China); Kang, Chunmei; Chen, Xiaojun; Wang, Heyi; Peng, Shuming [Institute of Nuclear Physics and Chemistry, China Academy of Engineering Physics, Box 919-214, Mian Yang 621900 (China); Wang, Xiaolin, E-mail: xlwang@caep.ac.cn [China Academy of Engineering Physics, Box 919-1, Mian Yang 621900 (China); Oya, Yasuhisa; Okuno, Kenji [Radiochemistry Research Laboratory, Faculty of Science, Shizuoka University, 836 Ohya, Shizuoka 422-8529 (Japan)

2013-07-15

Tritium release kinetics in lithium orthosilicate (Li{sub 4}SiO{sub 4}) ceramic pebbles irradiated with low thermal-neutron fluence was studied by out-of-pile annealing experiments. It was found that the tritium produced in Li{sub 4}SiO{sub 4} pebbles was mainly released as tritiated water vapor (HTO). The apparent desorption activation energy of tritium on the pebble surface was consistent with the diffusion activation energy of tritium in the crystal grains, indicating that tritium release was mainly controlled by diffusion process. The diffusion coefficients of tritium in the crystal grains at temperatures ranging from 450 K to 600 K were obtained by isothermal annealing tests, and the Arrhenius relation was determined to be D = 1 × 10{sup −7.0} exp (−40.3 × 10{sup 3}/RT) cm{sup 2} s{sup −1}.

Photoproduction of tritium

International Nuclear Information System (INIS)

Becker, J.A.; Anderson, J.D.; Weiss, M.S.

1995-01-01

3 H (Tritium) is required for maintenance of nuclear weapons in the stockpile. The National Defense need for 3 H was historically met by the Savannah River Facility. This facility is no longer safe for operation. 3 H decays with a mean lifetime τ = 17.8 y, and therefore new methods of 3 H production are required to meet US military requirements. Irradiation of 7 Li by low-energy photons produces tritium ( 3 H) via the photodisintegration process. Waste heat from the 7 Li target can be extracted and used for the direct generation of electricity. Other advantages include: negligible residual radioactivity, simple target technology, small low-energy electron accelerators for bremsstrahlung production (the photon source), developed liquid metal technology, modularity, simple extraction of 3 H from a recirculating 7 Li target, abundant supply of 7 Li, and straightforward target-accelerator-bremsstrahlung converter interface. A schematic plant characterized by very low risk is described, and a figure-of-merit is obtained

The influence of irradiation defects on tritium release from Li{sub 2}O

Energy Technology Data Exchange (ETDEWEB)

Tanaka, Satoru; Grishmanov, V [Tokyo Univ. (Japan). Faculty of Engineering

1996-10-01

During reactor irradiation of Li{sub 2}O defects are introduced by neutrons, triton and helium ions produced by {sup 6}Li(n, {alpha}){sup 3}H reactions and {gamma}-rays. Simultaneous measurements of luminescence emission and tritium release were performed under various conditions (temperature, sweep gas chemical composition) for Li{sub 2}O single crystal and polycrystal in order to elucidate possible influence of defects on tritium release. (author)

Tritium release behavior from neutron-irradiated Li{sub 2}TiO{sub 3} single crystal

Energy Technology Data Exchange (ETDEWEB)

Tanifuji, Takaaki; Yamaki, Daiju; Noda, Kenji [Japan Atomic Energy Research Inst., Tokai, Ibaraki (Japan). Tokai Research Establishment; Nasu, Shoichi

1998-03-01

Li{sub 2}TiO{sub 3} single-crystals with various size (1-2mm) were used as specimens. After the irradiation up to 4 x 10{sup 18} n/cm{sup 2} with thermal neutrons in JRR-2, tritium release from the Li{sub 2}TiO{sub 3} specimens in isothermal heating tests was continuously measured with a proportional counter. The tritium release in the range from 625K to 1373K seems to be controlled by bulk diffusion. The tritium diffusion coefficient (D{sub T}) in Li{sub 2}TiO{sub 3} was evaluated to be D{sub T}(cm{sup 2}/sec) = 0.100exp(-104(kJ/mol)/RT), 625Ktritium diffusion coefficients in Li{sub 2}TiO{sub 3} is almost equal to those of Li{sub 2}O irradiated with thermal neutrons up to 2 x 10{sup 19} n/cm{sup 2}. It indicates that the tritium release performance of Li{sub 2}TiO{sub 3} is essentially good as Li{sub 2}O. (author)

Final results phase II of the Mainz neutrino mass search in tritium ß decay

Czech Academy of Sciences Publication Activity Database

Kraus, Ch.; Bornschein, B.; Bornschein, L.; Bonn, J.; Flatt, B.; Kovalík, Alojz; Ostrick, B.; Otten, E.W.; Schall, J.P.; Thümmler, Th.; Weinheimer, Ch.

2005-01-01

Roč. 40, - (2005), s. 447-468 ISSN 1434-6001 R&D Projects: GA MŠk 1P04LA213 Institutional research plan: CEZ:AV0Z10480505 Keywords : neutrino mass * tritium beta decay Subject RIV: BG - Nuclear, Atomic and Molecular Physics, Colliders Impact factor: 1.659, year: 2005

Recent progress in the modelling of helium and tritium behaviour in irradiated beryllium pebbles

International Nuclear Information System (INIS)

Rabaglino, E.; Ronchi, C.; Cardella, A.

2003-01-01

One of the key issues of the European Helium Cooled Pebble Bed blanket is the behaviour under irradiation of beryllium pebbles, which have the function of neutron multiplier. An intense production of helium occurs in-pile, as well as a non negligible generation of tritium. Helium bubbles induce swelling and a high tritium inventory is a safety issue. Extensive studies for a better understanding, characterisation and modelling of the behaviour of helium and tritium in irradiated beryllium pebbles are being carried out, with the final aim to enable a reliable prediction of gas release and swelling in the full range of operating and accidental conditions of a Fusion Power Reactor. The general strategy consists in integrating studies on macroscopic phenomena (gas release) with the characterisation of corresponding microscopic diffusion phenomena (bubble kinetics) and the assessment of some fundamental diffusion parameter for the models (gas atomic diffusion coefficients). The present work gives a summary of the latest achievements in this context. By an inverse analysis of experimental out-of-pile gas release from weakly irradiated pebbles, coupled to the study of the characteristics of bubble population, it has been possible to assess the thermal diffusion coefficients of helium and tritium in and to improve and validate the classical model of gas precipitation into bubbles inside the grain. The improvement of the description of gas atomic diffusion and precipitation is the first step to enable a more reliable prediction of gas release

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)

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.

Experiments on tritium behavior in beryllium, (1)

International Nuclear Information System (INIS)

Kawamura, Hiroshi; Ishizuka, Etsuo; Matsumoto, Mikio; Inada, Seiji; Sezaki, Katsuji; Saito, Minoru; Kato, Mineo.

1989-06-01

In JMTR, it was observed that the tritium concentration of the primary coolant increases with the reactor operation at 50 MW. As one of the tritium generation sources, we paid attention to a neutron reflector made of beryllium because the tritium generation rate in the beryllium is bigger than other components in the reactor core. On the other hand, the irradiation test of blanket materials (i.e. tritium breeding materials and neutron multipling materials) are planned for development of the fusion reactor in JMTR and the beryllium will be also irradiated as a neutron multiplier with tritium breeding materials. Therefore, as the irradiated specimens, we used a hot-pressed beryllium disk fabricated by the same method as the neutron reflector or the neutron multiplier and conducted the irradiation tests in JMTR. The purpose of these tests are to clarify the tritium behavior in the hot-pressed beryllium. In this paper, from a viewpoint of the fabrication of capsules for neutron irradiation, the specifications of the irradiated specimens and capsules are summarized. Additionally, the results on the puncture test of the container of the irradiation specimens are described. (author)

High resolution studies by Secondary Ion Mass Spectrometry of the spatial distribution of tritium in neutron irradiated beryllium pebbles

International Nuclear Information System (INIS)

Rabaglino, E.; Tamborini, G.; Hiernaut, J.-P.; Betti, M.

2006-01-01

A key issue of beryllium as a neutron multiplier in the blanket of future fusion reactors is tritium retention. Models are under development in order to predict tritium release kinetics in the typical operating conditions of the material in the blanket: the absence of experimental data in this range imposes an extrapolation of the models, therefore a detailed characterization and understanding of microscopic diffusion phenomena related to macroscopic tritium release is necessary. It has been recently shown, that the availability of evidence on such phenomena at a scale of 1 micron down to tens of nanometers enables a relevant progress in the effectiveness of model validation: therefore the need for applying and developing advanced analytical techniques based on mass spectrometry at this scale. A study of tritium spatial distribution in neutron irradiated beryllium pebbles (2 mm diameter, 480 appm 4 He, 7 appm 3 H) by means of Secondary Ion Mass Spectrometry (SIMS) is presented. Samples in different conditions (non-irradiated, at end of irradiation and at different temperatures during thermal ramp annealing) are examined by an oxygen ion primary beam with a spatial resolution of 1 micron along a diameter. The sample preparation is optimized in order to enable a quantitative comparison among the different conditions. Under an oxygen ion beam tritium is detected in the irradiated samples in a molecular form (3H 2 ), with a continuous distribution inside the grains, which suggests the presence of small clusters in agreement with TEM analyses, and in the form of peaks at grain boundaries, corresponding to large grain boundary bubbles. The evolving of molecular tritium distribution measured by SIMS during a typical thermal ramp release experiment shows precisely tritium diffusion from the centre of the grain to grain boundaries as the temperature increases: at the same time the remaining intragranular tritium inventory, given by the integral of the distribution

Tritium release from beryllium pebbles after high temperature irradiation up to 3000 appm He in the HIDOBE-01 experiment

Energy Technology Data Exchange (ETDEWEB)

Til, S. van, E-mail: vantil@nrg.eu [Nuclear Research and Consultancy Group, Westerduinweg 3, Postbus 25, 1755 ZG Petten (Netherlands); Fedorov, A.V.; Stijkel, M.P.; Cobussen, H.L.; Mutnuru, R.K.; Idsert, P. van der [Nuclear Research and Consultancy Group, Westerduinweg 3, Postbus 25, 1755 ZG Petten (Netherlands); Zmitko, M. [The European Joint Undertaking for ITER and The Development of Fusion Energy, c/ Josep Pla, no. 2, Torres Diagonal Litoral, Edificio B3, 08019 Barcelona (Spain)

2013-11-15

In the HIDOBE (HIgh DOse irradiation of BEryllium) irradiation program, various grades of constrained and unconstrained beryllium pebbles, beryllium pellets and titanium-beryllide samples are irradiated in the High Flux Reactor (HFR) in Petten at four different temperatures (between 698 K and 1023 K) for 649 days [1]. The first of two HIDOBE irradiation experiments, HIDOBE-01, was completed after achieving a DEMO relevant helium production level of 3000 appm and the samples are retrieved for postirradiation examination (PIE). This work shows preliminary results of the out-of-pile tritium release analysis performed on different grades of irradiated beryllium pebbles (different in size). Relationships between irradiation temperature, tritium inventory and microstructural evolution have been observed by light microscopy and scanning electron microscopy.

Limit on the anti nu/sub e/ mass in free molecular tritium beta decay

International Nuclear Information System (INIS)

Bowles, T.J.; Wilkerson, J.F.; Browne, J.C.; Maley, M.P.; Robertson, R.G.H.; Knapp, D.A.; Helffrich, J.A.

1986-01-01

The question of a nonzero neutrino mass has received considerable attention since the claims of Lyubimov et al in 1980 were published which showed evidence for an electron antineutrino mass between 14 and 46 eV, with a best fit value of 35 eV. However, there are still considerable concerns about possible systematic problems in thier experiment. Many of these concerns revolve around the use of a tritiated valine source, in which the energy given up in final state excitations of the molecule following the veta decay of one of the tritium atoms is comparable to the size of the neutrino mass observed. The effect of these final state effects is difficult to calculate in a molecule as complex as valine. In addition, ionization energy loss and backscattering of the betas in traversing the solid source are appreciable and must be very accurately accounted for. These concerns have led us to carry out an experiment using free molecular tritium as the source material. The final state effects have been accurately calculated for the tritium molecule and the uncertainties in these calculations cannot generate a spurious neutrino mass greater than 1 eV. in addition, the energy loss in the source is small because the source consists of tritium only and there is no backscattering

Genotoxic and reprotoxic effects of tritium and external gamma irradiation on aquatic animals.

Science.gov (United States)

Adam-Guillermin, Christelle; Pereira, Sandrine; Della-Vedova, Claire; Hinton, Tom; Garnier-Laplace, Jacqueline

2012-01-01

Aquatic ecosystems are chronically exposed to natural radioactivity or to artificial radionuclides released by human activities (e.g., nuclear medicine and biology,nuclear industry, military applications). Should the nuclear industry expand in the future, radioactive environmental releases, under normal operating conditions or accidental ones, are expected to increase, which raises public concerns about possible consequences on the environment and human health. Radionuclide exposures may drive macromolecule alterations, and among macromolecules DNA is the major target for ionizing radiations. DNA damage, if not correctly repaired, may induce mutations, teratogenesis, and reproductive effects. As such, damage at the molecular level may have consequences at the population level. In this review, we present an overview of the literature dealing with the effects of radionuclides on DNA, development, and reproduction of aquatic organisms. The review focuses on the main radionuclides that are released by nuclear power plants under normal operating conditions, γ emitters and tritium. Additionally, we fitted nonlinear curves to the dose-response data provided in the reviewed publications and manuscripts, and thus obtained endpoints commonly associated with ecotoxicological studies, such as the EDR(10). These were then used as a common metric for comparing the values and data published in the literature.The effects of tritium on aquatic organisms were reviewed for dose rates that ranged from 29 nGy/day to 29 Gy/day. Although beta emission from tritium decay presents a rather special risk of damage to DNA, genotoxicity-induced by tritium has been scarcely studied. Most of the effects studied have related to reproduction and development. Species sensitivity and the form of tritium present are important factors that drive the ecotoxicity of tritium. We have concluded from this review that invertebrates are more sensitive to the effects of tritium than are vertebrates

Tritium-caused background currents in electron multipliers

International Nuclear Information System (INIS)

Malinowski, M.E.

1979-05-01

One channel electron multiplier (Galileo No. 4501) and one 14 stage Be/Cu multiplier (Dumont No. SPM3) were exposed to tritium pressures between approx. 10 -7 Torr to 10 -3 Torr in amounts from approx. 10 -5 Torr-s to 60 Torr-s and the β-decay caused currents in the multipliers measured. The background currents in both multipliers consisted of two components: (1) a high, reversible current which was proportional to the tritium exposure pressure; and (2) a lower, irreversible background current which increased with increasing cumulative tritium exposure. The β-decay caused currents in each multiplier increased the same way with exposure, suggesting the detected electrons arose from decaying tritium adsorbed on surfaced external to the multipliers

In situ tritium from Li2O and Li2ZrO3 irradiated in a fast neutron flux: BEATRIX-II, Phase 1 and 2

International Nuclear Information System (INIS)

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

1994-06-01

BEATRIX-II was an in situ tritium recovery experiment. This in situ tritium recovery experiment provided data on the performance of Li 2 O and Li 2 ZrO 3 under irradiation conditions covering a range of sweep gas compositions and temperatures. The experiment consisted of two separate irradiation cycles which in turn included two vented tritium recovery canisters each. Phase 1 operated for 300 Effective Full Power Days (EFPD) while Phase 2 operated for 203 EFPD of irradiation. The tritium recovery behavior of Li 2 O and Li 2 ZrO 3 was characterized using temperature transients, sweep gas composition changes and reactor power changes to effect changes in the tritium inventory. The high neutron flux level in FFTF resulted in high tritium generation rates which combined with a responsive tritium measurement system allowed detailed observations on the tritium recovery behavior of Li 2 O and Li 2 ZrO 3 . During the course of the experiment a number of observations were made which did not appear consistent with a simplified view of the tritium recovery behavior of these materials. These observations included small negative tritium recovery peaks preceding the typical primary positive peaks; and, for specific temperature ranges, changes in tritium inventory which where opposite to the characteristic expected changes

Tritium extraction from neutron-irradiated lithium aluminate.; Extraccion del tritio generado por irradiacion neutronica de aluminato de litio.

Energy Technology Data Exchange (ETDEWEB)

Garcia H, F

1995-10-01

Lithium aluminate is being strongly considered as a breeder material because of its thermophysical, chemical and mechanical stability at high temperatures and its favorable irradiation behavior. Furthermore, it is compatible with other blanket and structural materials. In this work, the effects of calcination temperature during preparation, extraction temperature and sweep gas composition were observed. Lithium aluminate prepared by four different methods, was neutron irradiated for 30 minutes at a flux of 10{sup 12} -10{sup 13} n/cm{sup 2} s in the TRIGA Mark III reactor at Salazar, Mexico; and the tritium extraction rate was measured. Calcination temperature do not affect the tritium extraction rate. However, using high calcination temperature, gamma lithium aluminate was formed. The tritium extraction at 600 Centigrade degrees was lower than at 800 Centigrade degrees and the tritium amount extracted by distillation of the solid sample was higher. The sweep gas composition showed that tritium extraction was less with Ar plus 0.5 % H{sub 2} that with Ar plus 0.1 % H{sub 2}. This result was contrary to expected, where the tritium extraction rate could be higher when hydrogen is added to the sweep gas. Probably this effect could be attributed to the gas purity. (Author).

LIBRETTO-3: Performance of tritium permeation barriers under irradiation at the HFR Petten

International Nuclear Information System (INIS)

Conrad, R.; Fuetterer, M.A.; Giancarli, L.; May, R.; Perujo, A.; Sample, T.

1994-01-01

The LIBRETTO-3 irradiation was performed at the HFR Petten during 77 full power days in three cycles to compare the efficiency of three different tritium permeation barriers in presence of Pb-17Li to uncoated AISI 316L steel. For this purpose four steel capsules (arnothing o =10 mm, arnothing i =8 mm, l=300 mm) were filled with 28 g Pb-17Li. The coatings included CVD TiC (outside), CVD TiC+Al 2 O 3 (inside), and pack cementation aluminisation (inside). The generated tritium was partly extracted by bubbling, partly it permeated through the capsules. Permeated and extracted tritium were measured as a function of temperature (280-450 C), H 2 doping (0-1 vol%) and purge gas flow rate. The driving partial pressure in the coated capsules were from an extraction model calibrated by the uncoated capsule for which tritium partial pressure could be calculated. In LIBRETTO-3 conditons, the best barrier was pack cementation aluminisation. The first interpretation of the experiment could, however, not confirm permeation reduction factors of 100 or more expected from this barrier. ((orig.))

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

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

Study on tritium recovery from breeder materials

International Nuclear Information System (INIS)

Moriyama, H.; Moritani, K.

1997-01-01

For the development of fusion reactor blanket systems, some of the key issues on the tritium recovery performance of solid and liquid breeder materials were studied. In the case of solid breeder materials, a special attention was focussed on the effects of irradiation on the tritium recovery performance, and tritium release experiments, luminescence measurements of irradiation defects and modeling studies were systematically performed. For liquid breeder materials, tritium recovery experiments from molten salt and liquid lithium were performed, and the technical feasibility of tritium recovery methods was discussed. (author)

Direct measurement of tritium production rate in LiPb with removed parasitic activities: Preliminary experiments

Energy Technology Data Exchange (ETDEWEB)

Kuc, Tadeusz, E-mail: kuc@agh.edu.pl; Pohorecki, Władysław; Ostachowicz, Beata

2014-10-15

Liquid scintillation (LS) technique applied to direct measurement of tritium activity produced in LiPb eutectic in Frascati HCLL TBM mock-up neutronic experiment has been tested so far in the case of LS measurement after long period since irradiation. LiPb samples irradiated in neutron filed show, except of tritium, meaningful activity of other radioisotopes (parasitic). Parasitic activity, mainly from isotopes of lead ({sup 209}Pb, {sup 204m}Pb, {sup 203}Pb) calculated with the use of FISPACT, exceeds ca 5 times tritium activity 1.4 h after irradiation. We propose to remove disturbing radioisotopes in a chemical way to avoid long “cooling” of the irradiated samples before tritium measurement. Samples (1 g of LiPb) irradiated in reactor fast neutron flux were diluted and metallic cations removed by chemical precipitation. For this purpose we used: potassium iodide (KJ), strontium chloride (SrCl{sub 2}), APDC (C{sub 5}H{sub 8}NS{sub 2}·NH{sub 4}), NaDDTC (C{sub 5}H{sub 10}NNaS{sub 2}·3H{sub 2}O), and PAN (C{sub 15}H{sub 11}N{sub 3}O). Precipitation procedure in each case lasted ca 5–25 min, and the following filtration next 10–20 min. In each filtrate (ca 120 ml) we measured Pb concentration in total reflection X-ray fluorescence (TXRF) analyzer and parasitic activity (left after 21-day “cooling”) applying HPGe gamma spectrometer. Pb cations precipitated by SrCl{sub 2} and than by PAN lowered activity of Pb isotopes to less than 1% of the initial tritium activity. Another combination of reagents: NaDDTC followed by SrCl{sub 2} in a single and double step filtration reduced Pb concentration 10{sup 2} and 10{sup 4} times, respectively. Reduction of this order allows tritium radiometric measurement ca 3 h after irradiation with acceptable accuracy. This time can be shortened by applying correction for decay of known parasitic activity. Input of {sup 76}As and other less abundant radioisotopes can be eliminated using high purity LiPb. Tritium activity of

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.)

Thermal-hydraulic calculation and analysis on helium cooled ceramic breeder pebble bed assembly for in-pile irradiation and in-situ tritium extraction

International Nuclear Information System (INIS)

Guo Chunqiu; Xie Jiachun; Liu Xingmin

2013-01-01

In-pile irradiation and in-situ tritium extraction experiment is one of associated domestic research projects in ITER special program. According to the technical requirements of in-pile irradiation experiment of helium cooled ceramic breeder (ceramic) pebble bed assembly in a research reactor, the feasibility of the design for the in-pile irradiation and in-situ tritium extraction experiment of ceramic pebble bed assembly was evaluated. By conducting thermal-hydraulic design calculation with different in-pile irradiation channels, locations and structure parameters for ceramic pebble bed assembly, a reasonable design scheme of ceramic pebble bed assembly satisfying the design requirements for in-pile irradiation was obtained. (authors)

An assembly of tritium production experiment

International Nuclear Information System (INIS)

Abe, Toshihiko

1981-01-01

An assembly for tritium production experiment, i.e. Tritium Extraction System (TREX) constructed as a small scale test facility for tritium production, and Tritium Removal System (TRS) attached to TREX, and the preliminary results of the experiments with them are described. The radiological safety of the process and operation is also an important consideration. Lithium-aluminum alloy was selected as the most promising target material. The following matters are involved in the scope of production technology: the selection of a target material and target preparation, reactor irradiation, the construction of a facility for the extraction of tritium from the irradiated target, the establishment of the optimum conditions of extraction, the purification, collection and storage of tritium, and the inspection of the product. The tritium production experiment at JAERI is yet on the initial stage; the development is to be continued with the stepwise increase of the scale of tritium production. (J.P.N.)

Study of tritium decontamination of stainless steel, copper, aluminum metals by tritium dry desorption

International Nuclear Information System (INIS)

Xie Yun; Shi Zhengkun; Wu Tao

2014-01-01

In order to study the decontamination efficiency of stainless steel, copper, aluminum metals contaminated by tritium, the metals were decontaminated by exposing to UV, ozone, heating, and the combination of heating, UV and ozone. The result indicates that the elevation of temperature can obviously improve decontamination. While irradiated by 172 nm UV, the decontamination efficiency is low, but it is better while heated and irradiated by 172 nm UV. If the stainless steel is irradiated by 172 nm UV and heated at 500℃ for 4 h, the decontamination efficiency is 99.2%. There is better decontamination efficiency of copper while exposed to ozone. While exposed to ozone and heated at 500℃, the decontamination efficiencies of stainless steel, copper and aluminum are higher than 99.2%. The decontamination efficiency can more obviously improve when metal is heated at high temperature (500℃) than low temperature (300℃). The surface tritium of metal placed at 30 d after decontamination increases because of diffusion and penetration of the tritium. Resolution spectra of tritium show that there are four kinds of contamination adsorbed tritium of stainless steel. (authors)

Removal of contaminating tritium and tritium pressure measurement by a secondary electron multiplier

International Nuclear Information System (INIS)

Ichimura, K.; Watanabe, K.; Nishizawa, K.; Fujita, J.

1984-01-01

A ceramic secondary electron multiplier (SEM), Ceratron, was used to study impairment of the SEM performance due to adsorbed tritium, its decontamination, and the applicability of the SEM to measure tritium pressure. The background level of the SEM increased significantly, up to its counting limit, due to tritium adsorption. Heating it to 300 0 C in vacuo and/or in the presence of reactive gases such as D 2 and CO at 1 x 10 -4 Pa was not effective to decontaminate the SEM, whereas photon irradiation was extremely powerful for the decontamination. The tritium (HT) pressure in a range of 1 x 10 -6 - 1 x 10 -3 Pa could be measured with no significant impairment of the SEM performance with the aid of photon irradiation. It is revealed that a particle flux as low as 1 particle/s will be able to measure in the presence of tritium if suitable photon sources are installed in the systems. (orig.)

Kinetics that govern the release of tritium from neutron-irradiated lithium oxide

International Nuclear Information System (INIS)

Bertone, P.C.

1986-01-01

The Lithium Blanket Module (LBM) program being conducted at the Princeton Plasma Physics Laboratory requires that tritium concentrations as low as 0.1 nCi/g, bred in both LBM lithium oxide pellets and gram-size lithium samples, be measured with an uncertainty not exceeding +/-6%. This thesis reports two satisfactory methods of assaying LBM pellets and one satisfactory method of assaying lithium samples. Results of a fundamental kinetic investigation are also reported. The thermally driven release of tritium from neutron-irradiated lithium oxide pellets is studied between the temperatures of 300 and 400 0 C. The observed release clearly obeys first-order kinetics, and the governing activation energy appears to be 28.4 kcal/mole. Finally, a model is presented that may explain the thermally driven release of tritium from a lithium oxide crystal and assemblies thereof. It predicts that under most circumstances the release is controlled by either the diffusion of a tritiated species through the crystal, or by the desorption of tritiated water from it

Tritium formation and elimination in light-water electronuclear plants

International Nuclear Information System (INIS)

Dolle, L.; Bazin, J.

1977-01-01

In light-water reactors, the tritium balance should be considered from both the working constraint and environmental pollution aspects. In light-water electronuclear stations with pressurized reactors using boric acid in solution for reactivity control, the amounts of tritium formed in the primary circuit are worthy of note. The estimations concerning the tritium production in a hypothetical 1000 MWe reactor are discussed. In the tritium build-up, the part which takes the tritium formed by fission in the fuel, owing to diffusion through cladding, is still difficult to estimate. The tritium balance in different working nuclear power stations are consequently of interest. But the tritium produced by ternary fission in the fuel is always much more abundant, and remains almost entirely confined in the uranium oxide if the fuel is clad with zircaloy. The annual quantity stored in the fuel elements is more than 20 times larger than that of the built up free tritium in the primary circuit water of a reactor. It reaches about 12,400 Ci in the hypothetical reactor. In the presently operated reprocessing plants, tritium is all going over in the effluents, and is almost entirely released in the environment. Taking into account the increasing quantities of high irradiated fuel to be reprocessed, it seems necessary to develop separation processes. Development work and tests have been achieved jointly by CEA and SAINT-GOBAIN TECHNIQUES NOUVELLES in order to: contain the tritium in the high activity part of the plant; and keep small the tritiated effluent volume, about 300 liters per ton of reprocessed uranium. It is then possible to envisage a storage for decay of isotopic separation processes. Such separation processes have been estimated by CEA assuming a daily output of 1500 liters of water containing 2,3 Ci.1 -1 of tritium, the desired decontamination factor being 100 [fr

Tritium release from EXOTIC-7 orthosilicate pebbles. Effect of burnup and contact with beryllium during irradiation

Energy Technology Data Exchange (ETDEWEB)

Scaffidi-Argentina, F; Werle, H [Forschungszentrum Karlsruhe GmbH Technik und Umwelt (Germany). Inst. fuer Neutronenphysik und Reaktortechnik

1998-03-01

EXOTIC-7 was the first in-pile test with {sup 6}Li-enriched (50%) lithium orthosilicate (Li{sub 4}SiO{sub 4}) pebbles and with DEMO representative Li-burnup. Post irradiation examinations of the Li{sub 4}SiO{sub 4} have been performed at the Forschungszentrum Karlsruhe (FZK), mainly to investigate the tritium release kinetics as well as the effect of Li-burnup and/or contact with beryllium during irradiation. The release rate of Li{sub 4}SiO{sub 4} from pure Li{sub 4}SiO{sub 4} bed of capsule 28.1-1 is characterized by a broad main peak at about 400degC and by a smaller peak at about 800degC, and that from the mixed beds of capsule 28.2 and 26.2-1 shows again these two peaks, but most of the tritium is now released from the 800degC peak. This shift of release from low to high temperature may be due to the higher Li-burnup and/or due to contact with Be during irradiation. Due to the very difficult interpretation of the in-situ tritium release data, residence times have been estimated on the basis of the out-of-pile tests. The residence time for Li{sub 4}SiO{sub 4} from caps. 28.1-1 irradiated at 10% Li-burnup agrees quite well with that of the same material irradiated at Li-burnup lower than 3% in the EXOTIC-6 experiment. In spite of the observed shift in the release peaks from low to high temperature, also the residence time for Li{sub 4}SiO{sub 4} from caps. 26.2-1 irradiated at 13% Li-burnup agrees quite well with the data from EXOTIC-6 experiment. On the other hand, the residence time for Li{sub 4}SiO{sub 4} from caps. 28.2 (Li-burnup 18%) is about a factor 1.7-3.8 higher than that for caps. 26.2-1. Based on these data on can conclude that up to 13% Li-burnup neither the contact with beryllium nor the Li-burnup have a detrimental effect on the tritium release of Li{sub 4}SiO{sub 4} pebbles, but at 18% Li-burnup the residence time is increased by about a factor three. (J.P.N.)

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.))

Experiments on tritium behavior in beryllium, (2)

International Nuclear Information System (INIS)

Ishitsuka, Etsuo; Kawamura, Hiroshi; Nakata, Hirokatsu; Sugai, Hiroyuki; Tanase, Masakazu.

1990-02-01

Beryllium has been used as the neutron reflector of material testing reactor and as the neutron multiplier for the fusion reactor lately. To study the tritium behavior in beryllium, we conducted the experiments, i.e., tritium release by recoil or diffusion by using the hot-pressed beryllium which had been produced both tritium and helium by neutron irradiation. From our experiments, we found that (1) amount of tritium production per one cycle irradiation (lasting 22 days) of JMTR is 10 mCi/g, (2) amount of tritium per surface area of hot-pressed beryllium released by recoil is 4 μCi/cm 2 , (3) diffusion coefficient of tritium in a temperature range of 800 ∼1180degC can be expressed with the following equation; D = 8.7 x 10 4 exp(-2.9x10 5 /R/T) cm 2 /s. (author)

Rapid heating tensile tests of high-energy-rate-forged 316L stainless steel containing internal helium from radioactive decay of absorbed tritium

International Nuclear Information System (INIS)

Mosley, W.C.

1990-01-01

316L stainless steel is a candidate material for construction of equipment that will be exposed to tritium. This austenitic stainless steel is frequently used in the high-energy-rate-forged (HERF) metallurgical condition to take advantage of increased strength produced by cold work introduced by this process. Proper design of tritium-handling equipment will require an understanding of how helium-3, the product of radioactive decay of tritium, affects mechanical properties. This report describes results of elevated-temperature tensile testing of HERF 316L stainless steel specimens containing helium concentrations of 171 (calculated) atomic parts per million (appm). Results are compared with those reported previously for specimens containing 0 and 94 (measured) appm helium

EXOTIC: Development of ceramic tritium breeding materials

International Nuclear Information System (INIS)

Kwast, H.; Conrad, R.

1989-09-01

In this fifth EXOTIC annual progress report the work carried out in 1988 is reported. For EXOTIC-1, -2 and -3 the post-irradiation examinations have been continued with tritium retention measurements, annealng experiments, determination of physical and mechanical properties and X-ray diffraction analysis. Irradiation of EXOTIC-4 has been performde and the post-irradiation examination has started. Transient tritium release curves are given and analysed. The resulting tritium residence times show that for the Li-zirconates a residence time of less than one day can be achieved in the temperature region of 350-600 C. The loading scheme, the objectives and some fabrication data of EXOTIC-5 are give. Moreover, the fabrication of laboratory scale batches has started to investigate the effect of microstructural parameters on tritium release. Finally, an investigation was started on the system Li 2 O-ZrO 2 , with emphasis on the lithia-rich compositions. 40 figs., 9 refs., 10 tabs

Progress report on the accelerator production of tritium materials irradiation program

International Nuclear Information System (INIS)

Maloy, S.A.; Sommer, W.F.; Brown, R.D.; Roberts, J.E.

1997-01-01

The Accelerator Production of Tritium (APT) project is developing an accelerator and a spoliation neutron source capable of producing tritium through neutron capture on He-3. A high atomic weight target is used to produce neutrons that are then multiplied and moderated in a blanket prior to capture. Materials used in the target and blanket region of an APT facility will be subjected to several different and mixed particle radiation environments; high energy protons (1-2 GeV), protons in the 20 MeV range, high energy neutrons, and low energy neutrons, depending on position in the target and blanket. Flux levels exceed 10 14 /cm 2 s in some areas. The APT project is sponsoring an irradiation damage effects program that will generate the first data-base for materials exposed to high energy particles typical of spallation neutron sources. The program includes a number of candidate materials in small specimen and model component form and uses the Los Alamos Spallation Radiation Effects Facility (LASREF) at the 800 MeV, Los Alamos Neutron Science Center (LANSCE) accelerator

Tritium transfer studies in cellulose-HTO system

International Nuclear Information System (INIS)

Jayaraman, A.P.; Misra, B.M.

1986-01-01

This paper describes some aspects of studies on transfer of tritium to cellulose from tritiated water at six different specific activities and discusses the generalized tritiation pattern. Cellulose was irradiated in steps to 10 M Rads and the tritium transfer was determined at each stage. Experimental results signify substantial increase of tritiation in cellulose at higher dose of irradiation. (author). 8 refs

Tritium target performance during an LBLOCA in a PWR

International Nuclear Information System (INIS)

Reid, B.D.

1996-01-01

In December 1995, the U.S. Department of Energy (DOE) announced a preferred strategy for acquiring a new supply of tritium. That strategy is based on pursuing the two most promising production alternatives. These alternatives include either constructing an accelerator-produced tritium system for tritium production or procuring an existing commercial light water reactor or irradiation services from such a reactor to irradiate tritium targets. This paper discusses the safety performance of a tritium target in a commercial pressurized water reactor (PWR). The current conceptual design for the light water tritium targets is quite similar, in terms of external dimensions and materials, to early designs for stainless steel clad discrete burnable absorbers used in PWRs. The tritium targets nominally consist of an annular lithium aluminate pellet wrapped in a Zircaloy-4 getter and clad with Type 316 stainless steel

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

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

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

Tritium ions in the Source and Transport Section (STS) of KATRIN

Energy Technology Data Exchange (ETDEWEB)

Klein, Manuel [Karlsruhe Institute of Technology (Germany); Collaboration: KATRIN-Collaboration

2016-07-01

The KArlsruhe TRItium Neutrino (KATRIN) experiment aims at the model independent measurement of the electron neutrino mass. It is designed for a neutrino mass sensitivity of 0.2 eV (90% CL) after three years of measurement time. KATRIN measures the end point of the tritium beta decay spectrum using a MAC-E filter and a Windowless Gaseous Tritium Source (WGTS). While neutral tritium gas molecules are pumped through the WGTS, the decay electrons are guided to the detector with a magnetic field. Tritium ions, however, also leave the WGTS following the magnetic field lines. For KATRIN measurements it is imperative to prevent tritium ions from reaching the detector or the spectrometers, where they could decay and cause an indistinguishable background. Ion blocking measures are implemented by electric blocking potentials and electric dipoles to drift out trapped ions. Their effective operation will be tested during KATRIN commissioning measurements: The ion flux between STS and spectrometers can be measured with the Forward Beam Monitor (FBM). It offers a manipulator arm to introduce a detector into the flux tube. For ion detection, a Faraday Cup for the FBM is being designed and constructed.

Status of the Los Alamos tritium beta decay experiment

International Nuclear Information System (INIS)

Robertson, R.G.H.; Bowles, T.J.; Wark, D.L.; Wilkerson, J.F.; Knapp, D.A.

1989-01-01

The Los Alamos tritium experiment employs a gaseous tritium source and a magnetic spectrometer to determine the mass of the electron antineutrino from the shape of the tritium beta spectrum. Since publication of the first result from this apparatus (m/sub nu/ < 27 eV at 95% confidence), work has concentrated on improving the data rates. A 96-element Si microstrip array detector has been installed to replace the single proportional counter at the spectrometer focus, resulting in greatly increased efficiency. Measurements of the 1s photoionization spectrum of Kr now obviate the need for reliance on the theoretical shakeup and shakeoff spectrum of Kr in determining the spectrometer resolution. 19 refs., 3 figs

2017 Accomplishments – Tritium Aging Studies on Stainless Steel Weldments and Heat-Affected Zones

Energy Technology Data Exchange (ETDEWEB)

Morgan, Michael J. [Savannah River Site (SRS), Aiken, SC (United States). Savannah River National Lab. (SRNL); Hitchcock, Dale [Savannah River Site (SRS), Aiken, SC (United States). Savannah River National Lab. (SRNL); Krentz, Tim [Savannah River Site (SRS), Aiken, SC (United States). Savannah River National Lab. (SRNL); McNamara, Joy [Savannah River Site (SRS), Aiken, SC (United States). Savannah River National Lab. (SRNL); Duncan, Andrew [Savannah River Site (SRS), Aiken, SC (United States). Savannah River National Lab. (SRNL)

2018-01-31

In this study, the combined effects tritium and decay helium in forged and welded Types 304L and 21-6-9 stainless steels were studied. To measure these effects, fracture mechanic specimens were thermally precharged with tritium and aged for approximately 17 years to build in decay helium from tritium decay prior to testing. The results are compared to earlier measurements on the same alloys and weldments (4-5, 8-9). In support of Enhanced Surveillance, “Tritium Effects on Materials”, the fracture toughness properties of long-aged tritium-charged stainless-steel base metals and weldments were measured and compared to earlier measurements. The fracture-toughness data were measured by thermally precharging as-forged and as-welded specimens with tritium gas at 34.5 MPa and 350°C and aging for approximately 17 years to build-in decay helium prior to testing. These data result from the longest aged specimens ever tested in the history of the tritium effects programs at Savannah River and the fracture toughness values measured were the lowest ever recorded for tritium-exposed stainless steel. For Type 21-6-9 stainless steel, fracture toughness values were reduced to less than 2-4% of the as-forged values to 41 lbs / in specimens that contained more than 1300 appm helium from tritium decay. The fracture toughness properties of long-aged weldments were also measured. The fracture toughness reductions were not as severe because the specimens did not retain as much tritium from the charging and aging as did the base metals. For Type 304L weldments, the specimens in this study contained approximately 600 appm helium and their fracture toughness values averaged 750 lbs / in. The results for other steels and weldments are reported and additional tests will be conducted during FY18.

Search for a rest mass of the electron antineutrino in the beta-decay of tritium

International Nuclear Information System (INIS)

Daniel, H.; Hiddemann, K.H.; Schwentker, O.

1986-01-01

The authors performed a precision measurement of the end point region of the tritium β-ray spectrum. The data were recorded with an iron-free π√13/2 magnetic spectrometer. The source consisted of tritium atoms, absorbed in a thin layer of hafnium, which was evaporated on a silicon wafer. The instrumental resolution was set to 0.1% in Δrho/rho. The fractional solid angle was 1% of 4π. The authors identified the electrons with a proportional counter, filled with isobutane. The counter had two distinct features: First, the good energy resolution of the signal at the main counting wire over a wide energy range allowed us to discriminate between real and background events, and second, there was a ring of several secondary counting wires around the main wire within the same gas volume, which served as an anticoincidence counter. With this arrangement an additional reduction of the background could be obtained. The functions of the spectrometer were checked by using internal conversion lines from the decay of /sup 169/Yb

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.

Screening effect as an explanation of results of Simpson experiment on tritium β decay

International Nuclear Information System (INIS)

Drukarev, E.G.; Strikman, M.I.

1989-01-01

Results of the work carried out by Simpson who observed a wide maximum in electron spectrum as a result of tritium decay in the range 0.75< T<1.5 keV are discussed. The results are not confirmed by the subsequent experiments. It is shown in the work that after correct account of interaction in finite state the discrepancy between experimental data and theoretical predictions for T ≥ 1 keV disappears. It is also shown that results at T<1 keV depend greatly on the effects of interaction with medium. Gross evaluation of the effects eliminates the discrepancy in the range 0.75< T<1 keV

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.

Tritium release from fast neutron irradiated boron carbide

International Nuclear Information System (INIS)

Hollenberg, G.W.

1977-01-01

A high-energy neutron reaction with boron produces tritium. In the LMFBR control material, B 4 C, most of the tritium that is generated remains in the pellets. Potential retention mechanisms are discussed. 5 figures

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

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)

In-situ tritium recovery from Li2O irradiated in fast neutron flux: BEATRIX-II initial results

International Nuclear Information System (INIS)

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

1990-10-01

The BEATRIX-II experiment in FFTF is an in-situ tritium recovery experiment to evaluate the tritium release characteristics of Li 2 O and its stability under fast neutron irradiation to extended burnups. This experiment includes two specimens: a thin annular specimen capable of temperature transients and a larger temperature gradient specimen. During the first 85 days of the operating cycle of the reactor, the tritium recovery rate of a temperature transient capsule was examined as a function of temperature, gas flow rate, gas composition and burnup. Temperature changes in the range from 525 to 625 degree C resulted in decreasing tritium inventory with increasing temperature. Lower gas flow rates resulted in slightly lower tritium release rates while gas composition changes affected the tritium release rate significantly, more than either flow rate or temperature changes. Three different sweep gases were used: He with 0.1% H 2 , He with 0.01% H 2 , and pure He. Decreasing the amount of hydrogen in the sweep gas decreased the steady-state release rate by as much as a factor of two. A temperature gradient capsule is more prototypic of the conditions expected in a fusion blanket and was designed to provide data that can be used in evaluating the operational parameters of a solid breeder in a blanket environment. The operation of this canister during the first 85 EFPD cycle suggests that Li 2 O is a viable solid breeder material. 9 refs., 5 figs., 3 tabs

Ion-molecular reactions initiated by β-decay of tritium in tritiated compounds

International Nuclear Information System (INIS)

Akulov, G.P.

1976-01-01

Ion-molecular reactions initiated by β-decay of tritium and tritiated hydrocarbons have been systematized. The review describes the theoretical and experimental foundation of the radiochemical method of this important type of chemical interactions investigation. The reactions of the molecular ions of HeT + with methane, ethane, propane, butane and also with cycloalkanes from C 3 to C 6 are discussed. The reactions under consideration have been united into two groups: reactions involving HeT + ions and those involving carbonic ions. From the experimental results available, the conclusions have been drawn about the reactivity of these intermediate formations, about the mechanism of their interaction with organic substances, and also about the perspectives of using the radiochemical method in studies of ion-molecular reactions. The experimental results published before May 1974 are examined. The bibliography includes 162 references

2016 Accomplishments. Tritium aging studies on stainless steel. Forging process effects on the fracture toughness properties of tritium-precharged stainless steel

Energy Technology Data Exchange (ETDEWEB)

Morgan, Michael J. [Savannah River Site (SRS), Aiken, SC (United States). Savannah River National Lab. (SRNL)

2017-01-01

Forged austenitic stainless steels are used as the materials of construction for pressure vessels designed to contain tritium at high pressure. These steels are highly resistant to tritium-assisted fracture but their resistance can depend on the details of the forging microstructure. During FY16, the effects of forging strain rate and deformation temperature on the fracture toughness properties of tritium-exposed-and-aged Type 304L stainless steel were studied. Forgings were produced from a single heat of steel using four types of production forging equipment – hydraulic press, mechanical press, screw press, and high-energy-rate forging (HERF). Each machine imparted a different nominal strain rate during the deformation. The objective of the study was to characterize the J-Integral fracture toughness properties as a function of the industrial strain rate and temperature. The second objective was to measure the effects of tritium and decay helium on toughness. Tritium and decay helium effects were measured by thermally precharging the as-forged specimens with tritium gas at 34.5 MPa and 350°C and aging for up to five years at -80°C to build-in decay helium prior to testing. The results of this study show that the fracture toughness properties of the as-forged steels vary with forging strain rate and forging temperature. The effect is largely due to yield strength as the higher-strength forgings had the lower toughness values. For non-charged specimens, fracture toughness properties were improved by forging at 871°C versus 816°C and Screw-Press forgings tended to have lower fracture toughness values than the other forgings. Tritium exposures reduced the fracture toughness values remarkably to fracture toughness values averaging 10-20% of as-forged values. However, forging strain rate and temperature had little or no effect on the fracture toughness after tritium precharging and aging. The result was confirmed by fractography which indicated that fracture modes

Tritium recovery from co-deposited layers using 193-nm laser

Science.gov (United States)

Shu, W. M.; Kawakubo, Y.; Nishi, M. F.

Recovery of tritium from co-deposited layers formed in deuterium-tritium plasma operations of the TFTR (Tokamak Fusion Test Reactor) was investigated by the use of an ArF excimer laser operating at the wavelength of 193 nm. At the laser energy density of 0.1 J/cm2, a transient spike of the tritium-release rate was observed at initial irradiation. Hydrogen isotopes were released in the form of hydrogen-isotope molecules during the laser irradiation in vacuum, suggesting that tritium can be recovered readily from the released gases. In a second experiment, hydrogen (tritium) recovery from the co-deposited layers on JT-60 tiles that had experienced hydrogen-plasma operations was investigated by laser ablation with a focused beam of the excimer laser. The removal rate of the co-deposited layers was quite low when the laser energy density was smaller than the ablation threshold (1.0 J/cm2), but reached 1.1 μm/pulse at the laser energy density of 7.6 J/cm2. The effective absorption coefficient in the co-deposited layers at the laser wavelength was determined to be 1.9 μm-1. The temperature of the surface during the irradiation at the laser energy density of 0.5 J/cm2 was measured on the basis of Planck's law of radiation, and the maximum temperature during the irradiation decreased from 3570 K at the initial irradiation to 2550 K at the 1000th pulse of the irradiation.

Quantitative analysis of tritium distribution in austenitic stainless steels welds

International Nuclear Information System (INIS)

Roustila, A.; Kuromoto, N.; Brass, A.M.; Chene, J.

1994-01-01

Tritium autoradiography was used to study the tritium distribution in laser and arc (TIG) weldments performed on tritiated AISI 316 samples. Quantitative values of the local tritium concentration were obtained from the microdensitometric analysis of the autoradiographs. This procedure was used to map the tritium concentration in the samples before and after laser and TIG treatments. The effect of the detritiation conditions and of welding on the tritium distribution in the material is extensively characterized. The results illustrate the interest of the technique for predicting a possible embrittlement of the material associated with a local enhancement of the tritium concentration and the presence of helium 3 generated by tritium decay. ((orig.))

Preparation of Tritium from irradiated lithium compounds (study)

International Nuclear Information System (INIS)

1989-01-01

The aim of the present study is the selection of a certain scheme for release, collection, measurement and analysis of Tritium as produced in Lithium compounds (Li 2 O, LiOH, Li 2 CO 3 LiF and some Lithium alloys) in accordance with the 6 Li(n, α)T reaction. Tritium technology is of vital concern to power reactor programmes as well as to fusion technology. Meanwhile the fields of activity include, tritium generation and mangement in fission and fusion reactors; enviromental studies, release modeling HT/HTO conversion and dose assessments, absorption/ deabsorption, monitoring and plant design; research and development, labeling, compatibility and physical chemical properties

Preparation of Tritium from irradiated lithium compounds (study)

Energy Technology Data Exchange (ETDEWEB)

1989-01-01

The aim of the present study is the selection of a certain scheme for release, collection, measurement and analysis of Tritium as produced in Lithium compounds (Li[sub 2]O, LiOH, Li[sub 2]CO[sub 3] LiF and some Lithium alloys) in accordance with the [sup 6]Li(n, [alpha])T reaction. Tritium technology is of vital concern to power reactor programmes as well as to fusion technology. Meanwhile the fields of activity include, tritium generation and mangement in fission and fusion reactors; enviromental studies, release modeling HT/HTO conversion and dose assessments, absorption/ deabsorption, monitoring and plant design; research and development, labeling, compatibility and physical chemical properties.

EXOTIC: Development of ceramic tritium breeding materials for fusion reactor blankets. The behaviour of tritium in: lithium aluminate, lithium oxide, lithium silicates, lithium zirconates

Energy Technology Data Exchange (ETDEWEB)

Kwast, H [Netherlands Energy Research Foundation (ECN), Petten (Netherlands); Stijkel, H [Netherlands Energy Research Foundation (ECN), Petten (Netherlands); Muis, R [Netherlands Energy Research Foundation (ECN), Petten (Netherlands); Conrad, R [Commission of the European Communities, Petten (Netherlands). Joint Reseach Centre

1995-12-01

This report describes the results of six EXOTIC experiments comprising a total of 48 capsules. Samples of the candidate tritium breeding materials LiAlO{sub 2}, Li{sub 2}ZrO{sub 3}, Li{sub 4}SiO{sub 4}, Li{sub 6}Zr{sub 2}O{sub 7}, Li{sub 8}ZrO{sub 6}, Li{sub 2}O and Li{sub 2}SiO{sub 3} have been irradiated at different temperature levels and up to a maximum lithium burnup of about 3%. Tritium residence times of the various breeding materials have been determined from temperature transients performed during irradiation. After irradiation the tritium inventory has been determined from small samples of the various materials. From the out-of-pile tritium release experiments activation energies were determined. These activities have been performed at ECN within the framework of the European Fusion Technology Programme on Breeding Blankets. (orig.).

Influence of radiation defects on tritium release parameters from Li2O

International Nuclear Information System (INIS)

Grishmanov, V.; Tanaka, S.; Yoneoka, T.

1998-01-01

The study of the influence of radiation defects on tritium release behavior from polycrystalline Li 2 O was performed by simultaneous measurements of the luminescence emission and tritium release. It was found that the radiation defects in Li 2 O introduced by electron irradiation cause the retention of tritium. It is thought that the tritium recovery is affected by the formation of a Li-T bond, which is tolerant of high temperatures. The retardation of tritium decreases with increasing absorbed dose in the dose range from 50 to 140 MGy. The aggregation of radiation defects at high irradiation doses is considered to be responsible for the decrease of the interaction of tritium with radiation defects. The mechanism of the interaction of radiation defects with tritium is discussed. (orig.)

Commercial Light Water Reactor -Tritium Extraction Facility Process Waste Assessment (Project S-6091)

Energy Technology Data Exchange (ETDEWEB)

Hsu, R.H.; Delley, A.O.; Alexander, G.J.; Clark, E.A.; Holder, J.S.; Lutz, R.N.; Malstrom, R.A.; Nobles, B.R. [Westinghouse Savannah River Co., Aiken, SC (United States); Carson, S.D. [Sandia National Laboratories, New Mexico, NM (United States); Peterson, P.K. [Sandia National Laboratories, New Mexico, NM (United States)

1997-11-30

The Savannah River Site (SRS) has been tasked by the Department of Energy (DOE) to design and construct a Tritium Extraction Facility (TEF) to process irradiated tritium producing burnable absorber rods (TPBARs) from a Commercial Light Water Reactor (CLWR). The plan is for the CLWR-TEF to provide tritium to the SRS Replacement Tritium Facility (RTF) in Building 233-H in support of DOE requirements. The CLWR-TEF is being designed to provide 3 kg of new tritium per year, from TPBARS and other sources of tritium (Ref. 1-4).The CLWR TPBAR concept is being developed by Pacific Northwest National Laboratory (PNNL). The TPBAR assemblies will be irradiated in a Commercial Utility light water nuclear reactor and transported to the SRS for tritium extraction and processing at the CLWR-TEF. A Conceptual Design Report for the CLWR-TEF Project was issued in July 1997 (Ref. 4).The scope of this Process Waste Assessment (PWA) will be limited to CLWR-TEF processing of CLWR irradiated TPBARs. Although the CLWR- TEF will also be designed to extract APT tritium-containing materials, they will be excluded at this time to facilitate timely development of this PWA. As with any process, CLWR-TEF waste stream characteristics will depend on process feedstock and contaminant sources. If irradiated APT tritium-containing materials are to be processed in the CLWR-TEF, this PWA should be revised to reflect the introduction of this contaminant source term.

Commercial Light Water Reactor -Tritium Extraction Facility Process Waste Assessment (Project S-6091)

International Nuclear Information System (INIS)

Hsu, R.H.; Delley, A.O.; Alexander, G.J.; Clark, E.A.; Holder, J.S.; Lutz, R.N.; Malstrom, R.A.; Nobles, B.R.; Carson, S.D.; Peterson, P.K.

1997-01-01

The Savannah River Site (SRS) has been tasked by the Department of Energy (DOE) to design and construct a Tritium Extraction Facility (TEF) to process irradiated tritium producing burnable absorber rods (TPBARs) from a Commercial Light Water Reactor (CLWR). The plan is for the CLWR-TEF to provide tritium to the SRS Replacement Tritium Facility (RTF) in Building 233-H in support of DOE requirements. The CLWR-TEF is being designed to provide 3 kg of new tritium per year, from TPBARS and other sources of tritium (Ref. 1-4).The CLWR TPBAR concept is being developed by Pacific Northwest National Laboratory (PNNL). The TPBAR assemblies will be irradiated in a Commercial Utility light water nuclear reactor and transported to the SRS for tritium extraction and processing at the CLWR-TEF. A Conceptual Design Report for the CLWR-TEF Project was issued in July 1997 (Ref. 4).The scope of this Process Waste Assessment (PWA) will be limited to CLWR-TEF processing of CLWR irradiated TPBARs. Although the CLWR- TEF will also be designed to extract APT tritium-containing materials, they will be excluded at this time to facilitate timely development of this PWA. As with any process, CLWR-TEF waste stream characteristics will depend on process feedstock and contaminant sources. If irradiated APT tritium-containing materials are to be processed in the CLWR-TEF, this PWA should be revised to reflect the introduction of this contaminant source term

Tritium isolation from lithium inorganic compounds applicable to thermonuclear reactor breeding blanket

International Nuclear Information System (INIS)

Vasil'ev, V.G.; Ershova, Z.V.; Nikiforov, A.S.

1982-01-01

Tritium separation from inorganic lithium compounds: Li 2 O, LiAlO 2 , Li 2 SiO 3 , Li 4 SiO 4 , LiF, LiBeF 3 , Li 2 BeF 4 irradiated with a beam of a gamma facility and a nuclear reactor, has been studied. In the first case the gas phase is absent. In the latter one- the tritium amount in the gas does not exceed 1-2% of its total amount in the salt. Based on the EPR spectra of irradiated salts the concentrations of paramagnetic centres are calculated. It is shown that during thermal annealing the main portion of tritium in the gas phase is in the form of oxide (HTO, T 2 O). Tritium is separated from lithium fluoroberyllates in the form of hydrogen (HT, T 2 ). The kinetics of tritium oxide isolation from irradiated lithium oxide aluminate, metha- and orthosilicates, lithium sulphate has been studied. The activation energies of tritium oxide separation process are presented. A supposition is made that chemical reaction of the HTO (T 2 O) or HT(T 2 ) or HF(TF) formation is a limiting stage. Clarification of the process stage limiting the rate of tritium recovery will permit to evaluate conditions for the optimum work of lithium material in the blanket, lithium zone to select the lithium element structure and temperature regime of irradiation

Lethal and Mutagenic Effects of Tritium Decay Produced by Tritiated Compounds Incorporated into Bacteria and Bacteriophages

Energy Technology Data Exchange (ETDEWEB)

Person, S. [Pennsylvania State University, University Park, PA (United States)

1968-06-15

The work discussed below is predominantly from the author's laboratory. Some effects of tritium decay on bacteria and bacteriophages, using labelled compounds that are incorporated preferentially into DNA, RNA or protein, have been studied. A relatively high killing efficiency, the probability that a single decay produces loss of colony-forming ability in bacteria or loss of plaque-forming ability in bacteriophages, is observed for thymidine- methyl-{sup 3}H decay, but this is thought to be due to S-particle ionization damage. The most definitive experiments involved a comparison of killing efficiencies for decays originating as thymidine-methyl-{sup 3}H in phage DNA and as amino acid-{sup 3}H in phage protein with the calculated {beta}-particle path length through, the DNA in the two cases. Experimental and calculated values are essentially the same. Radiation-dose calculations to many different bacterial sub-volumes were determined for several different distributions of radioactivity. The high killing efficiency for thymidine-methyl- {sup 3}H decay can be explained by {beta}-particle ionizations, providing DNA is the sensitive target molecule and it is organized in a central volume of the cell (see also Ref.[24]). Although both the lethal and mutagenic effect of thymidine-methyl-{sup 3}H and amino acid-{sup 3}H decays can readily be explained on the basis of {beta}-particle ionizations, the observed large mutation frequency produced by uracil-5{sup 3}H decay cannot. The majority of mutations produced by uracil-5{sup 3}H decays are due to a specific chemical rearrangement of the parent molecule, since decays from uracil-6{sup 3}H are 6 to 7-fold less mutagenic. It is clear that the decays leading to mutations for cells labelled with uracil-5{sup 3}H originate as cytosine-5{sup 3}H in bacterial DNA. Recent work shows that the specific chemical rearrangement causes a C --> T(u) genetic coding change. (author)

Analysis of decay of radicals induced in irradiated foods during long storage

International Nuclear Information System (INIS)

Kishita, Keigo; Kawamura, Shoei; Nakamura, Hideo; Ukai, Mitsuko; Kikuchi, Masahiro; Kobayashi, Yasuhiko

2013-01-01

By electron spin resonance (ESR) spectroscopy, we revealed free radicals in γ-ray irradiated foods ; black pepper, green coffee bean, cereal flour and ginseng. We also analyzed the decay behavior of radiation induced free radicals during long storage. The ESR spectrum of experimental irradiated foods consists of a sextet signal centered at g=2.0 and a singlet signal at the same g-value position and a singlet signal at g=4.0. The ESR spectrum of the cereal flour sample showed only singlet signal at g=2.0. The singlet signal at g=2.0 is originated from organic free radicals and its peak intensity showed the dependence of γ-ray radiation dose levels. But the signal intensity was decreased during storage. Only after 3 hours of radiation treatment the peak intensity was decreased fast and after that the intensity was decreased slowly. The analysis of radical decay process using the simulation methods based on the theory of reaction speed, the three decay behavior was showed. It is considered that at least three or more kinds of radicals were induced in irradiated foods and in decay during long time storage. (author)

Tritium retention properties of tungsten, graphite and co-deposited carbon film

International Nuclear Information System (INIS)

Nobuta, Y.; Hatano, Y.; Matsuyama, M.; Abe, S.; Akamaru, S.; Yamauchi, Y.; Hino, T.; Suzuki, S.; Akiba, M.

2014-01-01

DT + ion irradiation was performed on polycrystalline tungsten, graphite and carbon film and both the amount of retained tritium and the reduction of retained tritium after preservation in vacuum were investigated using an IP technique and BIXS. In addition, the relationship between the retention properties of tritium and the microstructure of graphite and carbon film were studied with Raman spectroscopy. The amount of retained tritium in tungsten was smaller than in both graphite and carbon film. After 1 keV of DT + irradiation, graphite showed no reduction of the amount of retained tritium after six months preservation while that of carbon film decreased by approximately 20% after 40 days preservation. It was suggested that this difference might be associated with differences in the microstructure between graphite and carbon film. In tungsten, the amount of retained tritium decreased to approximately half after 18 days preservation. As the incident energy of implanted tritium to tungsten increased, the decrease in tritium retention during preservation became slower. Tungsten's properties of releasing tritium while preserved in vacuum would be a useful tool for the reduction/removal of retained tritium

Advanced electrolytic cascade process for tritium recovery from irradiated heavy water moderator (Preprint No. PD-15)

International Nuclear Information System (INIS)

Ragunathan, P.; Mitra, S.K.; Jain, D.K.; Nayar, M.G.; Ramani, M.P.S.

1989-04-01

The paper briefly describes a design study of an electrolytic cascade process plant for enrichment and recovery of tritium from irradiated heavy water moderators from Rajasthan Atomic Power Station Reactors. In direct multistage electrolysis process, tritiated heavy water from the reactor units is fed to the electrolytic cell modules arranged in the form of a cascade where it is enriched and decomposed into O 2 gas stream and D 2 /DT gas stream. The direct electrolysis of tritiated heavy water allows tritium to be concentrated in the aqueous phase. Several stages are used to achieve the necessary enrichment. The cascade plant incorporates the advanced electrolyser technology developed in Bhabha Atomic Research Centre (Bombay) using porous nickel electrodes, capable o f high current density operation at reduced energy consumption for electrolysis. (author). 3 tabs

Tritium and helium-3 in metals

International Nuclear Information System (INIS)

Lasser, R.

1989-01-01

The book surveys recent results on the behaviour of tritium and its decay product helium-3 metals. In contrast to many earlier books which discuss the properties of the stable hydrogen isotopes without mentioning tritium, this book reviews mainly the results on tritium in metals. Due to the difficulties in preparing metal tritide samples, very important quantities such as diffusivity, superconductivity, solubility, etc. have only been determined very recently. The book not only presents the measured tritium data, but also the isotopic dependency of the different physical properties by comparing H, D and T results. A chapter is devoted to helium-3 in metals. Aspects such as helium release, generation of helium bubbles, swelling, and change of the lattice parameter upon aging are discussed. The book provides the reader with up-to-date information and deep insight into the behaviour of H, D, T and He-3 in metals. Further important topics such a tritium production, its risks, handling and discharge to the environment are also addressed

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

Introduction to Wolsong Tritium Removal Facility (WTRF)

International Nuclear Information System (INIS)

Song, K. M.; Sohn, S. H.; Kang, D. W.; Chung, H. S.

2005-01-01

Four CANDU 6 reactors have been operated at Wolsong site. Tritium is primarily produced in heavywater-moderated-power reactors by neutron capture of deuterium nuclei in the heavy water moderator and coolant. The concentration of tritium in the reactor moderator and coolant systems increases with time of reactor operation. For CANDU 6 reactors, the estimated equilibrium values are ∼3 TBq/kg-D 2 O in the moderator and ∼74 GBq/kg-D 2 O in the coolant, where the production rate is balanced by tritium decay and water makeup and loss process. The tritium level in the moderator heavy water of Wolsong Unit-1 is getting higher for about 20-year operation and is over 2.22x10 12 Bq/kg at the end of 2003. It was known that the tritium levels in the moderators of the other units would be also steadily increased. In order to reduce the tritium activity, KHNP has committed to construct a Tritium Removal Facility (TRF) at the Wolsong site

Calibrations of a tritium extraction facility

International Nuclear Information System (INIS)

Bretscher, M.M.; Oliver, B.M.; Farrar, H. IV.

1983-01-01

A tritium extraction facility has been built for the purpose of measuring the absolute tritium concentration in neutron-irradiated lithium metal samples. Two independent calibration procedures have been used to determine what fraction, if any, of tritium is lost during the extraction process. The first procedure compares independently measured 4 He and 3 H concentrations from the 6 Li(n,α)T reaction. The second procedure compared measured 6 Li(n,α)T/ 197 Au (n,γ) 198 Au thermal neutron reaction rate ratios with those obtained from Monte Carlo calculations using well-known cross sections. Both calibration methods show that within experimental errors (approx. 1.5%) no tritium is lost during the extraction process

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.

Tritium release kinetics of Li{sub 2}O with radiation defects

Energy Technology Data Exchange (ETDEWEB)

Grishmanov, V; Tanaka, Satoru [Tokyo Univ. (Japan). Faculty of Engineering

1998-03-01

The study of an influence of radiation defects on tritium release behavior from polycrystalline Li{sub 2}O was performed by the in-pile and out-of-pile tritium release experiments. The samples were pre-irradiated by accelerated electrons to various absorbed doses up to 140 MGy and then exposed to the fluence of 10{sup 17} thermal neutrons/m{sup 2}. The radiation defects introduced by electron irradiation in Li{sub 2}O cause the retention of tritium. The linear temperature increase of the electron-irradiated samples disclosed two tritium release peaks: first starts at {approx}600 K with the maximum at {approx}800 K and second appears at {approx}950 K with the maximum at {approx}1200 K. It is thought that the tritium release at high temperatures (> 950 K) is due to the thermal decomposition of LiT. In order to further investigated the formation of lithium hydrides, the diffuse-reflectance Fourier transform infrared (FTIR) absorption spectroscopy was applied. The Li{sub 2}O powder was irradiated by electron accelerator under D{sub 2} containing atmosphere (N{sub 2} + 10% D{sub 2}). An absorption band specific to the Li{sub 2}O was observed at 668 cm{sup -1} and attributed to the Li-D stretching vibration. (author)

Management of Tritium in ITER Waste

International Nuclear Information System (INIS)

Rosanvallon, S.; Benchikhoune, M.; Ciattaglia, S.; Uzan, J. Elbez; Na, B. C.; Taylor, N.; Gastaldi, O.

2011-01-01

ITER will use tritium as fuel. Procedures and processes are thus put in place in order to recover the tritium that is not used in the fusion reaction, including from waste and effluents. The tritium thus recovered can be re-injected into the fuel cycle. Moreover, tritium content and thus outgassing may be a safety concern, because of the potential for releases to the environment, both from the facility and from the final disposal (subjected to stringent acceptance criteria in the current waste final disposal). The aim of this paper is to present the measures considered to deal with the specific case of tritium in the liquid and solid waste that will arise from ITER operation and decommissioning. It concerns the processes that are considered from the waste production to its final disposal and in particular: the tritium removal stages (in-situ divertor baking at 350 C and tritium removal from solid waste and liquid and gaseous effluents), the removal of dust contamination (dust containing tritium produced by plasma-wall interaction and by the maintenance/ refurbishment processes) and the measures to enable safe processing and storage of the waste (wall-liner in the hot cell facility to limit concrete contamination and interim storage enabling tritium decay for waste that could not be directly accepted in the host-country final disposal facilities). (authors)

Tritium behavior in ITER beryllium

International Nuclear Information System (INIS)

Longhurst, G.R.

1990-10-01

The beryllium neutron multiplier in the ITER breeding blanket will generate tritium through transmutations. That tritium constitutes a safety hazard. Experiments evaluating tritium storage and release mechanisms have shown that most of the tritium comes out in a burst during thermal ramping. A small fraction of retained tritium is released by thermally activated processes. Analysis of recent experimental data shows that most of the tritium resides in helium bubbles. That tritium is released when the bubbles undergo swelling sufficient to develop porosity that connects with the surface. That appears to occur when swelling reaches about 10--15%. Other tritium appears to be stored chemically at oxide inclusions, probably as Be(OT) 2 . That component is released by thermal activation. There is considerable variation in published values for tritium diffusion through the beryllium and solubility in it. Data from experiments using highly irradiated beryllium from the Idaho National Engineering Laboratory showed diffusivity generally in line with the most commonly accepted values for fully dense material. Lower density material, planned for use in the ITER blanket may have very short diffusion times because of the open structure. The beryllium multiplier of the ITER breeding blanket was analyzed for tritium release characteristics using temperature and helium production figures at the midplane generated in support of the ITER Summer Workshop, 1990 in Garching. Ordinary operation, either in Physics or Technology phases, should not result in the release of tritium trapped in the helium bubbles. Temperature excursions above 600 degree C result in large-scale release of that tritium. 29 refs., 10 figs., 3 tabs

Analysis of tritium production in concentric spheres of oralloy and 6LiD irradiated by 14-MeV neutrons

International Nuclear Information System (INIS)

Fawcett, L.R. Jr.; Roberts, R.R. II; Hunter, R.E.

1988-03-01

Tritium production and activation of radiochemical detector foils in a sphere of 6 LiD with an oralloy core irradiated by a central source of 14-MeV neutrons have been calculated and compared with experimental measurements. The experimental assembly consisted of an oralloy sphere surrounded by three solid 6 LiD concentric shells with ampules of 6 LiH and 7 LiH and activation foils located in several positions throughout the assembly. The Los Alamos Monte Carlo Neutron Photon Transport Code (MCNP) was used to calculate neutron transport throughout the system, tritium production in the ampules, and foil activation. The overall experimentally observed-to-calculated ratios of tritium production were 0.996 +- 2.5% in 6 Li ampules and 0.903 +- 5.2% in 7 Li ampules. Observed-to-calculated ratios for foil activation are also presented. 11 refs., 4 figs., 7 tabs

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.

Simulation of alpha decay of actinides in iron phosphate glasses by ion irradiation

Energy Technology Data Exchange (ETDEWEB)

Dube, Charu L., E-mail: dubecharu@gmail.com; Stennett, Martin C.; Gandy, Amy S.; Hyatt, Neil C.

2016-03-15

Highlights: • Alpha decay of actinides in iron phosphate glasses is simulated by employing ion irradiation technique. • FTIR and Raman spectroscopic measurements confirm modification of glass network. • The depolymerisation of glass network after irradiation is attributed to synergetic effect of nuclear and electronic losses. - Abstract: A surrogate approach of ion beam irradiation is employed to simulate alpha decay of actinides in iron phosphate nuclear waste glasses. Bismuth and helium ions of different energies have been selected for simulating glass matrix modification owing to radiolysis and ballistic damage due to recoil atoms. Structural modification and change in coordination number of network former were probed by employing Reflectance Fourier-Transform Infrared (FT-IR), and Raman spectroscopies as a consequence of ion irradiation. Depolymerisation is observed in glass sample irradiated at intermediate energy of 2 MeV. Helium blisters of micron size are seen in glass sample irradiated at low helium ion energy of 30 keV.

New facility for post irradiation examination of neutron irradiated beryllium

International Nuclear Information System (INIS)

Ishitsuka, Etsuo; Kawamura, Hiroshi

1995-01-01

Beryllium is expected as a neutron multiplier and plasma facing materials in the fusion reactor, and the neutron irradiation data on properties of beryllium up to 800 degrees C need for the engineering design. The acquisition of data on the tritium behavior, swelling, thermal and mechanical properties are first priority in ITER design. Facility for the post irradiation examination of neutron irradiated beryllium was constructed in the hot laboratory of Japan Materials Testing Reactor to get the engineering design data mentioned above. This facility consist of the four glove boxes, dry air supplier, tritium monitoring and removal system, storage box of neutron irradiated samples. Beryllium handling are restricted by the amount of tritium;7.4 GBq/day and 60 Co;7.4 MBq/day

In-pile test of tritium recovery from lithium oxide

International Nuclear Information System (INIS)

Kurasawa, Toshimasa; Yoshida, Hiroshi; Watanabe, Hitoshi; Takeshita, Hidefumi; Miyauchi, Takejiro; Matsui, Tomoaki

1984-05-01

In-situ tritium recovery experiment with sintered lithium oxide pellets was performed under a high neutron fluence in the JRR-2. The irradiation hole VT-10 is the vertical one in the fuel rods region of the reactor, and the neutron flux is as follows: the thermal neutron flux with the epithermal neutron; 1.12 x 10 14 n/cm 2 . sec, the fast neutron flux; 1.0 x 10 12 n/cm 2 . sec. Irradiation material is the four pellets of cylindrical Li 2 O with the size of 11mm-OD, 1.8mm-ID, 10mm-H, and their total weight is 6.67g(the apparent bulk density 86%TD). A sweep gas capsule with a inner heater was constructed for the present study. Irradiation temperatures were regulated in the high temperature range, 470 -- 760 0 C. Four cycles of irradiation tests were carried out from May to August in 1983, and the effective thermal neutron fluence and the burnup of 6 Li were 5.9 x 10 19 nvt and 0.24% of total lithium(natural abundance of Li), respectively. The amount of generated tritium was calculated to be 31.2Ci by using a value of the depression factor of the thermal neutron flux(0.148) and the effective neutron cross section(543b) for the 6 Li(n, α) 3 H reaction. Present report describes the tritium release behavior in the in-situ tritium recovery apparatus and discuss the effects of the moisture, the hydrogen spiking, the irradiation temperature, etc.. Problems relative to a real time measurement of a comparatively high tritium concentration(10 -1 -- 10 2 μCi/cm 3 ) in the helium gas stream were also investigated. (author)

A study of tritium behavior in lithium oxide by ion conductivity measurements

International Nuclear Information System (INIS)

Noda, Kenji; Ishii, Yoshinobu; Ohno, Hideo; Watanabe, Hitoshi

1989-01-01

Ion conductivity of lithium oxide (Li 2 O) irradiated with oxygen ions was measured to obtain information about the effects of irradiation on the behavior of lithium ions and tritium. The conductivity around 490 K decreased with the ion fluence, while around 440 K it increased. The decrease around 490 K and the increase around 440 K were assumed to be attributed to the F + centers and the unspecified radiation defects, respectively. From the point of view that the rate determinant in the mechanism of diffusion of lithium ions in Li 2 O leading to the ion conductivity is the same as that of tritium, the diffusivity of tritium is assumed to be as follows: the diffusivity of tritium is decreased by the F + centers in the range from 490 K to the temperature at which almost all of F + centers are recovered, while it is increased around 440 K by the unspecified radiation defects. In addition, effects of the irradiation on valence states of tritium (i.e., T + , T - ) were discussed in terms of the radiation defects. (orig.)

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

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

Fluorine 18 in tritium generator ceramic materials

International Nuclear Information System (INIS)

Jimenez-Becerril, J.; Bosch, P.; Bulbulian, S.

1992-01-01

At present time, the ceramic materials generators of tritium are very interesting mainly by the necessity of to found an adequate product for its application as fusion reactor shielding. The important element that must contain the ceramic material is the lithium and especially the isotope with mass=6. The tritium in these materials is generated by neutron irradiation, however, when the ceramic material contains oxygen, then is generated too fluorine 18 by the action of energetic atoms of tritium in recoil on the 16 O, as it is showed in the next reactions: 1) 6 Li (n, α) 3 H ; 2) 16 O( 3 H, n) 18 F . In the present work was studied the LiAlO 2 and the Li 2 O. The first was prepared in the laboratory and the second was used such as it is commercially expended. In particular the interest of this work is to study the chemical behavior of fluorine-18, since if it would be mixed with tritium it could be contaminate the fusion reactor fuel. The ceramic materials were irradiated with neutrons and also the chemical form of fluorine-18 produced was studied. It was determined the amount of fluorine-18 liberated by the irradiated materials when they were submitted to extraction with helium currents and argon-hydrogen mixtures and also it was investigated the possibility about the fluorine-18 was volatilized then it was mixed so with the tritium. Finally it was founded that the liberated amount of fluorine-18 depends widely of the experimental conditions, such as the temperature and the hydrogen amount in the mixture of dragging gas. (Author)

Helium 3 precipitation in AISI 316L stainless steel induced by radioactive decay of tritium: Microstructural study of helium bubble precipitation

International Nuclear Information System (INIS)

Brass, A.M.; Chene, J.

1994-01-01

The development of the thermonuclear technology has given rise to a renewed interest in the study of the behavior of helium in metals. A great amount of work is still required for the understanding of the role of helium on the mechanical properties of structural materials for fusion technology, especially austenitic stainless steels. This article deals with the study of the influence of thermomechanical heat treatments, aging conditions (temperature and time), and helium concentration of helium bubble precipitation in a 316L austenitic steel. Helium was generated by the radioactive decay of tritium (tritium trick). Helium bubbles impede the grain growth in 316L steel aged at 1,373 K and also the recrystallization reaction at this temperature if cold working is performed prior to aging. Transmission electron microscopy (TEM) observations indicated a weak helium precipitation at 1,073 and 1,223 K, presumably due to the presence of trapping sites for tritium, and no bubble growth after aging up to 100 hours. Precipitation sites are mainly dislocations in the matrix at 1,073 K and grain boundaries and individual dislocations in the matrix at 1,223 K. The large bubble size (50 nm) observed at 1,373 K, even for short aging times (0.083), can partly be attributed to bubble dragging by dislocations toward the grain boundaries. Cold deformation prior to aging leads to a larger bubble size due to growth enhancement during recrystallization. Decreasing the helium content leads to a smaller helium bubble size and density. Tritium trapping at helium bubbles may favor helium 3 accumulation on defects such as grain boundaries, as observed by tritium autoradiography

Experimental method for investigating helium effects in irradiated vanadium

International Nuclear Information System (INIS)

Smith, D.L.; Matsui, H.; Greenwood, L.; Loomis, B.

1987-10-01

Analyses have been performed which indicate that an effective method for experimentally investigating helium effects in neutron irradiated vanadium base alloys can be developed. The experimental procedure involves only modest modifications to existing procedures currently used for irradiation testing of vanadium-base alloys in the FFTF reactor. Helium is generated in the vanadium alloy by decay of tritium which is either preinjected or generated within the test capsule. Calculations indicate that nearly constant He/dpa ratios of desired magnitude can be attained by proper selection of experimental parameters. The proposed method could have a major impact on the development of vanadium base alloys for fusion reactor applications. 8 refs., 4 figs

Use of Tritium Accelerator Mass Spectrometry for Tree Ring Analysis

Science.gov (United States)

LOVE, ADAM H.; HUNT, JAMES R.; ROBERTS, MARK L.; SOUTHON, JOHN R.; CHIARAPPA - ZUCCA, MARINA L.; DINGLEY, KAREN H.

2010-01-01

Public concerns over the health effects associated with low-level and long-term exposure to tritium released from industrial point sources have generated the demand for better methods to evaluate historical tritium exposure levels for these communities. The cellulose of trees accurately reflects the tritium concentration in the source water and may contain the only historical record of tritium exposure. The tritium activity in the annual rings of a tree was measured using accelerator mass spectrometry to reconstruct historical annual averages of tritium exposure. Milligram-sized samples of the annual tree rings from a Tamarix located at the Nevada Test Site are used for validation of this methodology. The salt cedar was chosen since it had a single source of tritiated water that was well-characterized as it varied over time. The decay-corrected tritium activity of the water in which the salt cedar grew closely agrees with the organically bound tritium activity in its annual rings. This demonstrates that the milligram-sized samples used in tritium accelerator mass spectrometry are suited for reconstructing anthropogenic tritium levels in the environment. PMID:12144257

Development of ITER Tritium Storage Material

Energy Technology Data Exchange (ETDEWEB)

Chung, H. C.; Kim, K. R.; Paek, S. W.; Shim, M.; Noh, B

2007-01-15

The ZrCo getter beds are built of a primary vessel which contains the ZrCo powder and of a secondary outer vessel. The purpose of the secondary outer vessel is to capture permeated or leaked tritium and to present a good thermal insulation when properly evacuated. A third volume, a helium filled loop, is installed in the primary volume to remove the decay heat and is used to perform tritium accountancy measurements. In this report the authors verified that ZrCo can be used safely under a low pressure and temperature.

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)

Description of tritium release from lithium titanate at constant temperature

Energy Technology Data Exchange (ETDEWEB)

Pena, L; Lagos, S; Jimenez, J; Saravia, E [Comision Chilena de Energia Nuclear, Santiago (Chile)

1998-03-01

Lithium Titanate Ceramics have been prepared by the solid-state route, pebbles and pellets were fabricated by extrusion and their microstructure was characterized in our laboratories. The ceramic material was irradiated in the La Reina Reactor, RECH-1. A study of post-irradiation annealing test, was performed measuring Tritium release from the Lithium Titanate at constant temperature. The Bertone`s method modified by R. Verrall is used to determine the parameters of Tritium release from Lithium Titanate. (author)

Nuclear irradiation parameters of beryllium under fusion, fission and IFMIF irradiation conditions

International Nuclear Information System (INIS)

Fischer, U.; Chen, Y.; Leichtle, D.; Simakov, S.; Moeslang, A.; Vladimirov, P.

2004-01-01

A computational analysis is presented of the nuclear irradiation parameters for Beryllium under irradiation in typical neutron environments of fission and fusion reactors, and of the presently designed intense fusion neutron source IFMIF. The analysis shows that dpa and Tritium production rates at fusion relevant levels can be achieved with existing high flux fission reactors while the achievable Helium production is too low. The resulting He-Tritium and He/dpa ratios do not meet typical fusion irradiation conditions. Irradiation simulations in the medium flux test modules of the IFMIF neutron source facility were shown to be more suitable to match fusion typical irradiation conditions. To achieve sufficiently high production rates it is suggested to remove the creep-fatigue testing machine together with the W spectra shifter plate and move the tritium release module upstream towards the high flux test module. (author)

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

Influence of hot water dip and gamma irradiation on postharvest fungal decay of Galia melons

International Nuclear Information System (INIS)

Barkai-Golan, R.; Padova, R.; Ross, I.; Lapidot, M.; Copel, A.; Davidson, H.

1993-01-01

Dipping Galia melons in hot water at 52 deg C for 5 min or at 55 deg for 2 min resulted in 12-15% decay (caused by Alternaria alternata, Fusarium spp. and Trichothecium roseum) during prolonged storage (12 d at 6 deg plus 3 d at 18 deg ) compared with 75% decay in untreated fruit or 60% decay in cold-water-dipped fruit. Irradiation at 0.5 or 1 kGy had no significant effect on decay development. However, combination of heat treatment with a 0.5 kGy dose prevented fungal growth, resulting in 5% decay during storage. Combinations of heating with 1 kGy irradiation gave no improvement in anti-fungal effect over treatment with 0.5 kGy and sometimes resulted in a decreased suppressive effect. Reducing the duration of dipping at 55 deg from 2 to 0.5 min, applied alone or in combination with irradiation, considerably reduced the anti-fungal effect of the treatment. The effective combined treatment resulted in 12-15% of slight peel damage, but all the fruits were regarded as marketable. No differences in fruit firmness were recorded among the treatments

Calibration of an experimental model of tritium storage bed designed for 'in situ' accountability

International Nuclear Information System (INIS)

Bidica, Nicolae; Stefanescu, Ioan; Bucur, Ciprian; Bulubasa, Gheorghe; Deaconu, Mariea

2009-01-01

Full text: Objectives: Tritium accountancy of the storage beds in tritium facilities is an important issue for tritium inventory control. The purpose of our work was to perform calibration of an experimental model of tritium storage bed with a special design, using electric heaters to simulate tritium decay, and to evaluate the detection limit of the accountancy method. The objective of this paper is to present an experimental method used for calibration of the storage bed and the experimental results consisting of calibration curves and detection limit. Our method is based on a 'self-assaying' tritium storage bed. The basic characteristics of the design of our storage bed consists, in principle, of a uniform distribution of the storage material on several copper thin fins (in order to obtain a uniform temperature field inside the bed), an electrical heat source to simulate the tritium decay heat, a system of thermocouples for measuring the temperature field inside the bed, and good thermal isolation of the bed from the external environment. Within this design of the tritium storage bed, the tritium accounting method is based on determining the decay heat of tritium by measuring the temperature increase of the isolated storage bed. Experimental procedure consisted in measuring of temperature field inside the bed for few values of the power injected with the aid of electrical heat source. Data have been collected for few hours and the temperature increase rate was determined for each value of the power injected. Graphical representation of temperature rise versus injected powers was obtained. This accounting method of tritium inventory stored as metal tritide is a reliable solution for in-situ tritium accountability in a tritium handling facility. Several improvements can be done regarding the design of the storage bed in order to improve the measurement accuracy and to obtain a lower detection limit as for instance use of more accurate thermocouples or special

Fusion reactor start-up without an external tritium source

Energy Technology Data Exchange (ETDEWEB)

Zheng, S., E-mail: Shanliang.Zheng@ccfe.ac.uk; King, D.B.; Garzotti, L.; Surrey, E.; Todd, T.N.

2016-02-15

Highlights: • Investigated the feasibility (including plasma physics, neutronics and economics) of starting a fusion reactor from running pure D–D fusion reactor to gradually move towards the D–T operation. • Proposed building up tritium from making use of neutrons generated by D–D fusion reactions. • Studied plasma physics feasibility for pure D–D operation and provided consistent fusion power and neutron yield in the plasma with different mixture of deuterium and tritium. • Discussed the economics aspect for operating a pure D–D fusion reactor towards a full-power D–T fusion reactor. - Abstract: It has long been recognised that the shortage of external tritium sources for fusion reactors using D–T, the most promising fusion fuel, requires all such fusion power plants (FPP) to breed their own tritium. It is also recognised that the initial start-up of a fusion reactor will require several kilograms of tritium within a scenario in which radioactive decay, ITER and subsequent demonstrator reactors are expected to have consumed most of the known tritium stockpile. To circumvent this tritium fuel shortage and ultimately achieve steady-state operation for a FPP, it is essential to first accumulate sufficient tritium to compensate for loss due to decay and significant retention in the materials in order to start a new FPP. In this work, we propose to accumulate tritium starting from D–D fusion reactions, since D exists naturally in water, and to gradually build up the D–T plasma targeted in fusion reactor designs. There are two likely D–D fusion reaction channels, (1) D + D → T + p, and (2) D + D → He3 + n. The tritium can be generated via the reaction channel ‘(1)’ and the 2.45 MeV neutrons from ‘(2)’ react with lithium-6 in the breeding blanket to produce more tritium to be fed back into plasma fuel. Quantitative evaluations are conducted for two blanket concepts to assess the feasibility and suitability of this approach to FPP

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

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.

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

Tritium release from lithium ceramics at constant temperature

International Nuclear Information System (INIS)

Verrall, R.A.; Miller, J.M.

1992-02-01

Analytic methods for post-irradiation annealing tests to measure tritium release from lithium ceramics at constant temperature are examined. Modifications to the Bertone (1) relations for distinguishing diffusion-controlled release from desorption-controlled release are shown. The methods are applied to tests on sintered LiA10 2 ; first-order desorption is shown to control tritium release for these tests

Tritium Storage Material

International Nuclear Information System (INIS)

Cowgill, Donald F.; Luo, Weifang; Smugeresky, John E.; Robinson, David B.; Fares, Stephen James; Ong, Markus D.; Arslan, Ilke; Tran, Kim L.; McCarty, Kevin F.; Sartor, George B.; Stewart, Kenneth D.; Clift, W. Miles

2008-01-01

Nano-structured palladium is examined as a tritium storage material with the potential to release beta-decay-generated helium at the generation rate, thereby mitigating the aging effects produced by enlarging He bubbles. Helium retention in proposed structures is modeled by adapting the Sandia Bubble Evolution model to nano-dimensional material. The model shows that even with ligament dimensions of 6-12 nm, elevated temperatures will be required for low He retention. Two nanomaterial synthesis pathways were explored: de-alloying and surfactant templating. For de-alloying, PdAg alloys with piranha etchants appeared likely to generate the desired morphology with some additional development effort. Nano-structured 50 nm Pd particles with 2-3 nm pores were successfully produced by surfactant templating using PdCl salts and an oligo(ethylene oxide) hexadecyl ether surfactant. Tests were performed on this material to investigate processes for removing residual pore fluids and to examine the thermal stability of pores. A tritium manifold was fabricated to measure the early He release behavior of this and Pd black material and is installed in the Tritium Science Station glove box at LLNL. Pressure-composition isotherms and particle sizes of a commercial Pd black were measured.

EXOTIC: Development of ceramic tritium breeding materials

International Nuclear Information System (INIS)

Flipot, A.J.; Kennedy, P.; Conrad, R.

1989-03-01

As part of the joint European Programme on fusion blanket technology three laboratories, Northern Research Laboratories (NRL), Springfields in the UK, SCK/CEN-Mol in Belgium and ECN-Petten in conjunction with JRC-Petten in the Netherlands have worked closely together since 1983 on the development of ceramic breeder materials, the programme being codenamed EXOTIC. Lithium oxides, aluminates, silicates and zirconates have been produced, characterised and irradiated in the HFR-Petten in experiments EXOTIC-1, -2 and -3. EXOTIC-4 is in preparation. In this fourth annual progress report the work achieved in 1987 is reported. For EXOTIC-1 to -3 mainly post irradiation examinations have been carried out like: visual inspection, puncturing of closed capsules, tritium retention measurements and material characterisation. Moreover, tritium release experiments on small specimens have started. SCK/CEN performed a general study on lithium silicates, in particular on the thermal stability. Finally, the fabrication and the characterisation of the materials to be irradiated in experiment EXOTIC-4 are presented. The eight capsules of EXOTIC-4 will be loaed with samples of Li 2 SiO 3 , Li 2 O, Li 2 ZrO 3 , Li 6 Zr 2 O 7 and Li 8 ZrO 6 . The irradiation will last 4 reactor cycles or about 100, Full Power Day, FPD. The main objective is to determine the tritium residence time of the various lithium zirconates. 18 figs., 8 refs., 15 tabs

Report on the evaluation of the tritium producing burnable absorber rod lead test assembly. Revision 1

International Nuclear Information System (INIS)

1997-03-01

This report describes the design and fabrication requirements for a tritium-producing burnable absorber rod lead test assembly and evaluates the safety issues associated with tritium-producing burnable absorber rod irradiation on the operation of a commercial light water reactor. The report provides an evaluation of the tritium-producing burnable absorber rod design and concludes that irradiation can be performed within U.S. Nuclear Regulatory Commission regulations applicable to a commercial pressurized light water reactor

Toxicity of tritium

International Nuclear Information System (INIS)

Dobson, R.L.

1979-01-01

Among radionuclides of importance in atomic energy, 3 H has relatively low toxicity. The main health and environmental worry is the possibility that significant biological effects may follow from protracted exposure to low concentrations in water. To examine this possible hazard and measure toxicity at low tritium concentrations, chronic exposure studies were done on mice and monkeys. During vulnerable developmental periods animals were exposed to 3 HOH, and mice were exposed also to 60 Co gamma irradiation and energy-related chemical agents. The biological endpoint measured was the irreversible loss of female germ cells. Effects from tritium were observed at surprisingly low concentrations where 3 H was found more damaging than previously thought. Comparisons between tritium and gamma radiation showed the relative biological effectiveness (RBE) to be greater than 1 and to reach approximately 3 at very low exposures. For perspective, other comparisons were made: between radiation and chemical agents, which revealed parallels in action on germ cells, and between pre- and postnatal exposure, which warn of possible special hazard to the fetus from both classes of energy-related byproducts

Tritium measurement technique using ''in-bed'' calorimetry

International Nuclear Information System (INIS)

Klein, J.E.; Mallory, M.K.; Nobile, A. Jr.

1991-01-01

One of the new technologies that has been introduced to the Savannah River Site (SRS) is the production scale use of metal hydride technology to store, pump, and compress hydrogen isotopes. For tritium stored in metal hydride storage beds, a unique relationship does not exist between the amount of tritium in the bed and the pressure-volume-temperature properties of the hydride material. Determining the amount of tritium in a hydride bed after desorbing the contents of the bed to a tank and performing pressure, volume, temperature, and composition (PVTC) measurements is not practical due to long desorption/absorption times and the inability to remove tritium ''heels'' from the metal hydride materials under normal processing conditions. To eliminate the need to remove tritium from hydride storage beds for measurement purposes, and ''in-bed'' tritium calorimetric measurement technique has been developed. The steady-state temperature rise of a gas stream flowing through a jacketed metal hydride storage bed is measured and correlated with power input to electric heaters used to simulate the radiolytic power generated by the decay of tritium to 3 He. Temperature rise results for prototype metal hydride storage beds and the effects of using different gases in the bed are shown. Linear regression results shows that for 95% confidence intervals, temperature rise measurements can be obtained in 14 hours and have an accuracy of ±1.6% of a tritium filled hydride storage bed

Basic study of influence of radiation defects on tritium release processes from lithium silicates

Energy Technology Data Exchange (ETDEWEB)

Abramenkovs, A.; Tiliks, J.; Kizane, G.; Supe, A. [Latvia Univ., Riga (Latvia). Dept. of Chem.; Grishmanovs, V. [Department of Quantum Engineering and System Science, The University of Tokyo, 7-3-1 Hongo, Bunkyo-ku, Tokyo 113 (Japan)

1997-09-01

The radiolysis of Li{sub 2}SiO{sub 3} and Li{sub 4}SiO{sub 4} was studied using the chemical scavengers method (CSM), thermoluminescence, lyoluminescence, electron spin resonance and spectrometric methods. The influence of the absorbed dose and many another parameters such as: irradiation conditions, sample preparation conditions and concentration of impurities on the accumulation rate of each type RD and RP were studied. Several possibilities for reducing the radiolysis of silicates were discussed. It has been found that tritium localization on the surface and in grains proceed by two different mechanisms. Tritium thermoextraction from the surface proceeds as chemidesorption of tritiated water, but from the bulk as diffusion. The tritium retention processes were studied. It has been found that tritium retention depends on irradiation conditions. Tritium retention is due to the formation of chemical bonds Li-T and thermal stable {identical_to}Si-T bonds. The accumulation of colloidal silicon and lithium can increase the tritium retention up to 25-35%. (orig.).

Kinetics of free radical decay reactions in lactic acid homo and copolymers irradiated to sterilization dose

International Nuclear Information System (INIS)

Kantoglu, O.; Ozbey, T.; Gueven, O.

1995-01-01

The kinetics of free radical decay reactions of poly(L-Lactic acid), poly(DL-Lactic acid) and random copolymer of lactic and glycolic acid have been investigated for decays taking place in air and in vacuum. The change in ESR lines of γ-irradiated polymers have been followed over a long time period. The decay has been found to follow neither simple first-order nor second-order kinetics. Various kinetic approaches including composite first or second-order mechanisms and diffusion-controlled first or second-order equations were determined to be also unsatisfactory. The decay of radicals in bulk irradiated lactic acid homo and copolymers was found to be best described when the second-order non-classical equation with time dependent rate constant approach was used. (Author)

Retention and release of tritium in aluminum clad, Al-Li alloys

International Nuclear Information System (INIS)

Louthan, M.R. Jr.

1991-01-01

Tritium retention in and release from aluminum clad, aluminum-lithium alloys is modeled from experimental and operational data developed during the thirty plus years of tritium production at the Savannah River Site. The model assumes that tritium atoms, formed by the 6 Li(n,α) 3 He reaction, are produced in solid solution in the Al-Li alloy. Because of the low solubility of hydrogen isotopes in aluminum alloys, the irradiated Al-Li rapidly becomes supersaturated in tritium. Newly produced tritium atoms are trapped by lithium atoms to form a lithium tritide. The effective tritium pressure required for trap or tritide stability is the equilibrium decomposition pressure of tritium over a lithium tritide-aluminum mixture. The temperature dependence of tritium release is determined by the permeability of the cladding to tritium and the local equilibrium at the trap sites. This model is used to calculate tritium release from aluminum clad, aluminum-lithium alloys. 9 refs., 3 figs

Tritium biological effects and perspective of the biological study

International Nuclear Information System (INIS)

Komatsu, Kenshi

1998-01-01

Since tritium is an emitter of weak β-rays (5.7keV) and is able to bind to DNA, i.e., the most important genome component, the biological effects should be expected to be more profound than that of X-rays and γ-rays. When carcinogenesis, genetical effects and the detriments for fetus and embryo were used as a biological endpoint, most of tritium RBE (relative biological effectiveness) ranged from 1 to 2. The tritium risk in man could be calculated from these RBEs and γ-ray risk for human exposure, which are obtained mainly from the data on Atomic Bomb survivors. However, the exposure modality from environmental tritium should be a chronic irradiation with ultra low dose rate or a fractionated irradiation. We must estimate the tritium effect in man based on biological experiments alone, due to lack of such epidemiological data. Low dose rate experiment should be always accompanied by the statistical problem of data, since their biological effects are fairy low, and they should involve a possible repair system, such as adaptive response (or hormesis effect) and 'Kada effect' observed in bacteria. Here we discuss future works for the tritium assessment in man, such as (1) developing a high radiation sensitive assay system with rodent hybrid cells containing a single human chromosome and also (2) study on mammal DNA repair at molecular levels using a radiosensitive hereditary disease, Nijmegen Breakage Syndrome. (author)

Tritium trapping states induced by lithium-depletion in Li{sub 2}TiO{sub 3}

Energy Technology Data Exchange (ETDEWEB)

Kobayashi, Makoto, E-mail: kobayashi.makoto@LHD.nifs.ac.jp [National Institute for Fusion Science (Japan); Oya, Yasuhisa; Okuno, Kenji [Radioscience Research Laboratory, Faculty of Science, Shizuoka University, Shizuoka (Japan)

2017-04-15

Identifications of tritium trapping states in neutron-irradiated Li{sub 1.8}TiO{sub 2.9} (lithium-depleted Li{sub 2}TiO{sub 3}) were carried out by the out-of-pile tritium release behavior. Tritium release behaviors for neutron-irradiated Li{sub 2}TiO{sub 3} and tritium gas-exposed TiO{sub 2} were also measured for comparison. Among the tritium release spectra for these samples, three tritium release peaks were appeared. By the kinetic analyses of tritium release behaviors, the Arrhenius parameters for three peaks were evaluated. Especially for Li{sub 1.8}TiO{sub 2.9}, there were two tritium release peaks, and the peak in lower temperature region was assigned to the tritium release controlled by the diffusion process in Li{sub 2}TiO{sub 3} structure. The other tritium release peak, which was hardly appeared for Li{sub 2}TiO{sub 3}, was assigned to the release of tritium trapped as hydroxyl groups in Li{sub 1.8}TiO{sub 2.9}, indicating that lithium-depletion would result in the formation of hydroxyl groups in Li{sub 2}TiO{sub 3}. Lithium vacancies existed in Li{sub 2}TiO{sub 3} crystal structure would promote the tritium trapping as hydroxyl groups due to the decreased charge repulsion between lithium ions and tritium ion, resulting in the difficulty of recovering tritium from Li{sub 2}TiO{sub 3} effectively.

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.)

In-Pile Assemblies for Investigation of Tritium Release from Li2TiO3 Lithium Ceramic

International Nuclear Information System (INIS)

Shestakov, V.; Tazhibayeva, I.; Kawamura, H.; Kenzhin, Y.; Kulsartov, T.; Chikhray, Y.; Kolbaenkov, A.; Arinkin, F.; Gizatulin, Sh.; Chakrov, P.

2005-01-01

The description of algorithm to design in-pipe experimental ampoule devices (IPAD) is presented here, including description of IPAD design for irradiation tests of highly enriched lithium ceramics at WWR-K reactor. The description of the system for registration of tritium release from ceramics during irradiation is presented as well. Typical curve of tritium release from the IPAD during irradiation under various temperatures of the samples is shown here

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)

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)

Systematic preservation of teeth and prophylaxis of dental decay on irradiated patients

International Nuclear Information System (INIS)

Horiot, J.C.; Schraub, S.

1975-01-01

200 patients were irradiated on the oral cavity and on salivary glands with doses of 3,000Rads and up. Teeth were preserved. A prophylactic treatment of dental decay was made using 5 minutes daily a fluoride gel into a carrier. The results showed an incidence of 5% for dental decay and 1% for osteo-radionecroses. Details are given about the selection of patients, the dental work-up and dental care before, during and after radiation therapy [fr

Modeling of tritium behavior in Li2O

International Nuclear Information System (INIS)

Billone, M.C.; Attaya, H.; Kopasz, J.P.

1992-08-01

The TIARA and DISPL2 codes are being developed at Argonne National Laboratory to predict tritium retention and release from lithium ceramics under steady-state and transient conditions, respectively. Tritium retention and release are important design and safety issues for tritium-breeding blankets of fusion reactors. Emphasis has been placed on tritium behavior in Li 2 O because of the selection of this ceramic as a first option for the ITER driver blanket and because of the relatively good material properties data base for Li 2 O. Models and correlations for diffusion, surface desorption/adsorption, and solubility/precipitation of tritium in Li 2 0 have been developed based on well-controlled laboratory data from as-fabricated and irradiated samples. With the models and correlations, the codes are validated to the results of in-reactor purge flow tests. The results of validation of TIARA to tritium retention data from VOM-15H, EXOTIC-2, and CRITIC-1 are presented, along with predictions of tritium retention in BEATRIX-II. For DISPL2, results are presented for tritium release predictions vs. data for MOZART, CRITIC-1, and BEATRIX-II. Recommendations are made for improving both the data base and the modeling to allow extrapolation with reasonable uncertainty levels to fusion reactor design conditions

Cellular- and micro-dosimetry of heterogeneously distributed tritium.

Science.gov (United States)

Chao, Tsi-Chian; Wang, Chun-Ching; Li, Junli; Li, Chunyan; Tung, Chuan-Jong

2012-01-01

The assessment of radiotoxicity for heterogeneously distributed tritium should be based on the subcellular dose and relative biological effectiveness (RBE) for cell nucleus. In the present work, geometry-dependent absorbed dose and RBE were calculated using Monte Carlo codes for tritium in the cell, cell surface, cytoplasm, or cell nucleus. Penelope (PENetration and Energy LOss of Positrins and Electrons) code was used to calculate the geometry-dependent absorbed dose, lineal energy, and electron fluence spectrum. RBE for the intestinal crypt regeneration was calculated using a lineal energy-dependent biological weighting function. RBE for the induction of DNA double strand breaks was estimated using a nucleotide-level map for clustered DNA lesions of the Monte Carlo damage simulation (MCDS) code. For a typical cell of 10 μm radius and 5 μm nuclear radius, tritium in the cell nucleus resulted in much higher RBE-weighted absorbed dose than tritium distributed uniformly. Conversely, tritium distributed on the cell surface led to trivial RBE-weighted absorbed dose due to irradiation geometry and great attenuation of beta particles in the cytoplasm. For tritium uniformly distributed in the cell, the RBE-weighted absorbed dose was larger compared to tritium uniformly distributed in the tissue. Cellular- and micro-dosimetry models were developed for the assessment of heterogeneously distributed tritium.

Deuterium-tritium fuel self-sufficiency in fusion reactors

International Nuclear Information System (INIS)

Abdou, M.A.; Vold, E.L.; Gung, C.Y.; Youssef, M.Z.; Shin, K.

1986-01-01

Conditions necessary to achieve deuterium-tritium fuel self-sufficiency in fusion reactors are derived through extensive modeling and calculations of the required and achievable tritium breeding ratios as functions of the many reactor parameters and candidate design concepts. It is found that the excess margin in the breeding potential is not sufficient to cover all present uncertainties. Thus, the goal of attaining fuel self-sufficiency significantly restricts the allowable parameter space and design concepts. For example, the required breeding ratio can be reduced by (A) attaining high tritium fractional burnup, >5%, in the plasma, (B) achieving very high reliability, >99%, and very short times, <1 day, to fix failures in the tritium processing system, and (C) ensuring that nonradioactive decay losses from all subsystems are extremely low, e.g., <0.1% for the plasma exhaust processing system. The uncertainties due to nuclear data and calculational methods are found to be significant, but they are substantially smaller than those due to uncertainties in system definition

2009 EVALUATION OF TRITIUM REMOVAL AND MITIGATION TECHNOLOGIES FOR WASTEWATER TREATMENT

Energy Technology Data Exchange (ETDEWEB)

LUECK KJ; GENESSE DJ; STEGEN GE

2009-02-26

Since 1995, a state-approved land disposal site (SALDS) has received tritium contaminated effluents from the Hanford Site Effluent Treatment Facility (ETF). Tritium in this effluent is mitigated by storage in slow moving groundwater to allow extended time for decay before the water reaches the site boundary. By this method, tritium in the SALDS is isolated from the general environment and human contact until it has decayed to acceptable levels. This report contains the 2009 update evaluation of alternative tritium mitigation techniques to control tritium in liquid effluents and groundwater at the Hanford site. A thorough literature review was completed and updated information is provided on state-of-the-art technologies for control of tritium in wastewaters. This report was prepared to satisfy the Hanford Federal Facility Agreement and Consent Order (Tri-Party Agreement) Milestone M-026-07B (Ecology, EPA, and DOE 2007). Tritium separation and isolation technologies are evaluated periodically to determine their feasibility for implementation to control Hanford site liquid effluents and groundwaters to meet the Us. Code of Federal Regulations (CFR), Title 40 CFR 141.16, drinking water maximum contaminant level (MCL) for tritium of 20,000 pOll and/or DOE Order 5400.5 as low as reasonably achievable (ALARA) policy. Since the 2004 evaluation, there have been a number of developments related to tritium separation and control with potential application in mitigating tritium contaminated wastewater. These are primarily focused in the areas of: (1) tritium recycling at a commercial facility in Cardiff, UK using integrated tritium separation technologies (water distillation, palladium membrane reactor, liquid phase catalytic exchange, thermal diffusion), (2) development and demonstration of Combined Electrolysis Catalytic Exchange (CECE) using hydrogen/water exchange to separate tritium from water, (3) evaporation of tritium contaminated water for dispersion in the

Future use of tritium in mapping pre-bomb groundwater volumes.

Science.gov (United States)

Eastoe, C J; Watts, C J; Ploughe, M; Wright, W E

2012-01-01

The tritium input to groundwater, represented as volume-weighted mean tritium concentrations in precipitation, has been close to constant in Tucson and Albuquerque since 1992, and the decrease in tritium concentrations at the tail end of the bomb tritium pulse has ceased. To determine the future usefulness of tritium measurements in southwestern North America, volume-weighted mean tritium levels in seasonal aggregate precipitation samples have been gathered from 26 sites. The averages range from 2 to 9 tritium units (TU). Tritium concentrations increase with site latitude, and possibly with distance from the coast and with site altitude, reflecting local ratios of combination of low-tritium moisture advected from the oceans with high-tritium moisture originating near the tropopause. Tritium used alone as a tool for mapping aquifer volumes containing only pre-bomb recharge to groundwater will become ambiguous when the tritium in precipitation at the end of the bomb tritium pulse decays to levels close to the analytical detection limit. At such a time, tritium in precipitation from the last one to two decades of the bomb pulse will become indistinguishable from pre-bomb recharge. The threshold of ambiguity has already arrived in coastal areas with a mean of 2 TU in precipitation and will follow in the next three decades throughout the study region. Where the mean tritium level is near 5 TU, the threshold will occur between 2025 and 2030, given a detection limit of 0.6 TU. Similar thresholds of ambiguity, with different local timing possible, apply globally. © 2011, The Author(s). Ground Water © 2011, National Ground Water Association.

DP-THOT - a calculational tool for bundle-specific decay power based on actual irradiation history

International Nuclear Information System (INIS)

Johnston, S.; Morrison, C.A.; Albasha, H.; Arguner, D.

2005-01-01

A tool has been created for calculating the decay power of an individual fuel bundle to take account of its actual irradiation history, as tracked by the fuel management code SORO. The DP-THOT tool was developed in two phases: first as a standalone executable code for decay power calculation, which could accept as input an entirely arbitrary irradiation history; then as a module integrated with SORO auxiliary codes, which directly accesses SORO history files to retrieve the operating power history of the bundle since it first entered the core. The methodology implemented in the standalone code is based on the ANSI/ANS-5.1-1994 formulation, which has been specifically adapted for calculating decay power in irradiated CANDU reactor fuel, by making use of fuel type specific parameters derived from WIMS lattice cell simulations for both 37 element and 28 element CANDU fuel bundle types. The approach also yields estimates of uncertainty in the calculated decay power quantities, based on the evaluated error in the decay heat correlations built-in for each fissile isotope, in combination with the estimated uncertainty in user-supplied inputs. The method was first implemented in the form of a spreadsheet, and following successful testing against decay powers estimated using the code ORIGEN-S, the algorithm was coded in FORTRAN to create an executable program. The resulting standalone code, DP-THOT, accepts an arbitrary irradiation history and provides the calculated decay power and estimated uncertainty over any user-specified range of cooling times, for either 37 element or 28 element fuel bundles. The overall objective was to produce an integrated tool which could be used to find the decay power associated with any identified fuel bundle or channel in the core, taking into account the actual operating history of the bundles involved. The benefit is that the tool would allow a more realistic calculation of bundle and channel decay powers for outage heat sink planning

Process for recovering tritium from molten lithium metal

Science.gov (United States)

Maroni, Victor A.

1976-01-01

Lithium tritide (LiT) is extracted from molten lithium metal that has been exposed to neutron irradiation for breeding tritium within a thermonuclear or fission reactor. The extraction is performed by intimately contacting the molten lithium metal with a molten lithium salt, for instance, lithium chloride - potassium chloride eutectic to distribute LiT between the salt and metal phases. The extracted tritium is recovered in gaseous form from the molten salt phase by a subsequent electrolytic or oxidation step.

Investigation of hydrogen isotopes interaction processes with lithium under neutron irradiation

Energy Technology Data Exchange (ETDEWEB)

Zaurbekova, Zhanna, E-mail: zaurbekova@nnc.kz [Institute of Atomic Energy, National Nuclear Center of RK, Kurchatov (Kazakhstan); Skakov, Mazhyn; Ponkratov, Yuriy; Kulsartov, Timur; Gordienko, Yuriy; Tazhibayeva, Irina; Baklanov, Viktor; Barsukov, Nikolay [Institute of Atomic Energy, National Nuclear Center of RK, Kurchatov (Kazakhstan); Chikhray, Yevgen [Institute of Experimental and Theoretical Physics of Kazakh National University, Almaty (Kazakhstan)

2016-11-01

Highlights: • The experiments on study of helium and tritium generation and release processes under neutron irradiation from lithium saturated with deuterium are described in paper. ​ • The values of relative tritium and helium yield from lithium sample at different levels of neutron irradiation is calculated. • It was concluded that the main affecting process on tritium release from lithium is its interaction with lithium atoms with formation of lithium tritide. - Abstract: The paper describes the experiments on study of helium and tritium generation and release processes from lithium saturated with deuterium under neutron irradiation (in temperature range from 473 to 773 K). The diagrams of two reactor experiments show the time dependences of helium, DT, T{sub 2}, and tritium water partial pressures changes in experimental chamber with investigated lithium sample. According to experimental results, the values of relative tritium and helium yield from lithium sample at different levels of neutron irradiation were calculated. The time dependences of relative tritium and helium yield from lithium sample were plotted. It was concluded that the main affecting process on tritium release from lithium is its interaction with lithium atoms with formation of lithium tritide.

Tritium in the Savannah River Site environment. Revision 1

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.

Tritium target manufacturing for use in accelerators

Science.gov (United States)

Bach, P.; Monnin, C.; Van Rompay, M.; Ballanger, A.

2001-07-01

As a neutron tube manufacturer, SODERN is now in charge of manufacturing tritium targets for accelerators, in cooperation with CEA/DAM/DTMN in Valduc. Specific deuterium and tritium targets are manufactured on request, according to the requirements of the users, starting from titanium target on copper substrate, and going to more sophisticated devices. A wide range of possible uses is covered, including thin targets for neutron calibration, thick targets with controlled loading of deuterium and tritium, rotating targets for higher lifetimes, or large size rotating targets for accelerators used in boron neutron therapy. Activity of targets lies in the 1 to 1000 Curie, diameter of targets being up to 30 cm. Special targets are also considered, including surface layer targets for lowering tritium desorption under irradiation, or those made from different kinds of occluders such as titanium, zirconium, erbium, scandium, with different substrates. It is then possible to optimize either neutron output, or lifetime and stability, or thermal behavior.

Adaptive responses induced in bone marrow and blood of the rats by tritium contamination

International Nuclear Information System (INIS)

Savu, D.I.; Ionescu, M.A.; Petcu, I.

2000-01-01

It has been more than a decade since the initial report on the phenomenon termed 'adaptive response to ionizing radiation'. Although a number of reports have appeared since then, the understanding of this response is still incomplete. Our group intended to investigate whether the adaptive response could be induced in vivo by low level internal tritium contamination of rats and subsequently exposed to challenging irradiations with fast neutrons or gamma rays. Two experiments were performed and analysed comparatively. In the first experiment the rats have been pre-contaminated for 3 weeks to total doses of 7 cGy and 35 cGy and subsequently irradiated to 1 Gy by fast neutrons (d(13.5)+Be). They were sacrificed after 24 hours. In the second experiment rats were exposed to high gamma irradiation (1.4 Gy) after prior contamination with tritium for 20 days to total doses of 4.4 cGy and 5.1 cGy. We followed up the modifications of two biochemical parameters: (i) the in vitro tritiated thymidine incorporation in the bone marrow cells and (ii) the reduced glutathione level in the blood cells. The thymidine incorporation assay revealed a putative adaptive reaction only for the rats preirradiated with tritiated water to 35 cGy and post-irradiated with fast neutrons. The glutathione content was found to be increased (back to the normal level) for the tritium pre-contaminated and neutron irradiated animals as compared to those exposed only to fast neutrons. The adaptive response is believed to be a protective mechanism that confers resistance to the detrimental effects of ionizing radiation. Our studies suggest that the irradiation with low conditioning doses of tritium (7; 35 cGy) is more efficient in conferring radioresistance to bone marrow and blood cells at the treatment with fast neutrons (1 Gy) than the irradiation with tritium doses of 4.4 and 5.1 cGy followed by gamma rays (1.4 Gy). (authors)

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

Radiolytic unsaturation decay in polyethylene. Part II--the effect of irradiation temperature, thermal history and orientation

International Nuclear Information System (INIS)

Lyons, Bernard J.

2004-01-01

The decay rate of vinyl unsaturation in high-density polyethylenes irradiated at temperatures from about 310 to 450 K, changes significantly in the melting range up to the crystalline melting point as does free radical mobility and the polymer crystallinity. However, orienting the polymer, or slow cooling or quenching from the melt, prior to irradiation, do not alter the decay process or its rate, although they do alter the rate of increase of insoluble gel and of elastic modulus in the molten state. It is suggested that, below ∼340 K, the marked deviations from a first-order decay result from the limited mobility of polymeric free radicals in the crystalline phase and from scavenging, by vinyl groups, segregated into the amorphous phase, of radiolytic hydrogen atoms (H). In the melting range, the mobility of polymeric free radicals increases as the crystallinity decreases, reducing the importance of scavenging, so vinyl decay approximates more closely to a first-order relation. In the melt, the vinyl decay relation is not changed qualitatively by H atom scavenging, but the effective vinyl concentration is lower, so the decay rate drops sharply

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

Decay of organic free radicals in γ-ray irradiated pepper during thermal treatment as detected by electron spin resonance spectroscopy

International Nuclear Information System (INIS)

Ukai, Mitsuko; Shimoyama, Yuhei

2004-01-01

Using electron spin resonance (ESR) spectroscopy we analysed the thermal decay process of radicals in γ-Irradiated pepper Upon irradiation, the satellite signals were newly induced and appeared at the symmetric positions of the organic free radical, i.e., the g=2.0 signal. Heat treatment decreased the satellite signals exponentially. The ESR signal of the pepper heated for more than 10 min was essentially the same as that before irradiation. To evaluate the radical decay by heat-treatment, we formulated a time-dependent master equation. We could evaluate the time constant of the radical decay based upon the general solution of the equation together with the nonlinear least-squares method

Technology benefits resulting from accelerator production of tritium

International Nuclear Information System (INIS)

1998-01-01

One of the early and most dramatic uses of nuclear transformations was in development of the nuclear weapons that brought World War II to an end. Despite that difficult introduction, nuclear weapons technology has been used largely as a deterrent to war throughout the latter half of the twentieth century. The Accelerator Production of Tritium (APT) offers a clean, safe, and reliable means of producing the tritium (a heavy form of hydrogen) needed to maintain the nuclear deterrent. Tritium decays away naturally at a rate of about 5.5% per year; therefore, the tritium reservoirs in nuclear weapons must be periodically replenished. In recent years this has been accomplished by recycling tritium from weapons being retired from the stockpile. Although this strategy has served well since the last US tritium production reactor was shut down in 1988, a new tritium production capability will be required within ten years. Some benefits will result from direct utilization of some of the APT proton beam; others could result from advances in the technologies of particle accelerators and high power spallation targets. The APT may save thousands of lives through the production of medical isotopes, and it may contribute to solving the nation's problem in disposing of long-lived nuclear wastes. But the most significant benefit may come from advancing the technology, so that the great potential of accelerator applications can be realized during our lifetimes

Isothermal release of tritium from neutron-irradiated Li/sub 2/O pellets

Energy Technology Data Exchange (ETDEWEB)

O' Hira, Shigeru; Nagao, Hiroshi; Fujii, Yasuhiko; Okamoto, Makoto

1986-04-01

Li/sub 2/O pellets irradiated with thermal neutrons were isothermally annealed to release tritium in a helium atmosphere at temperatures ranging from 673 to 1073 K. The release rates were found to significantly increase at elevated temperatures and to depend on the density of the Li/sub 2/O pellet. The overall diffusion coefficients of the release process were calculated using the cylindrical geometry model for the pellets as D(cm/sup 2/ s/sup -1/)=1.02 x 10/sup -3/ exp(-51.0 kJ mol/sup -1//RT)(90% theoretical density pellets), and D (cm/sup 2/ s/sup -1/)=2.64 x 10/sup -3/ exp(-46.5 kJ mol/sup -1//RT)(ca. 80% T.D. pellets) over the region 773 <= T <= 1073/sup 0/K. The result of the release experiment at 673/sup 0/K sugested that the diffusion rate was controlled by the decomposition of lithium hydroxide on the surface of Li/sub 2/O grains.

Consideration of disposal alternatives for tritium-contaminated wastewater streams at Hanford

International Nuclear Information System (INIS)

Waters, E.D.

1988-03-01

Small quantities of tritium are produced as an undesirable by-product of the operation of light-water reactors. At the US Department of Energy Hanford Site in Washington State, some tritium has been discharged to the environment in low-level liquid and gaseous wastes from the N Reactor plant, but more than 97% of the tritium stays typically within the irradiated fuel as it is delivered for reprocessing. During fuel reprocessing, the tritium is distributed in the process streams, and most of the tritium is presently released to the soil column with excess process condensates from the Plutonium-Uranium Extraction (PUREX) Plant. On an annual basis, approximately 1 g of tritium is discharged in more than 1 x 10 6 L of process condensate water. Principal tritium release points and quantities are presented in section 4.0. The present study is intended to identify and evaluate alternate methods of tritium control and disposal that might merit additional study or development for potential application to Hanford Site effluents. 30 refs., 15 figs., 5 tabs

Tritium Assay and Dispensing of KEPRI Tritium Lab

International Nuclear Information System (INIS)

Sohn, S. H.; Song, K. M.; Lee, S. K.; Lee, K.W.; Ko, B. W.

2009-01-01

The Wolsong Tritium Removal Facility(WTRF) has been constructed to reduce tritium levels in the heavy water systems and environmental emissions at the site. The WTRF was designed to process 100 kg/h of heavy water with the overall tritium extraction efficiency of 97% per single pass and to produce ∼700 g of tritium as T2 per year at the feed concentration of 0.37 TBq/kg. The high purity tritium greater than 99% is immobilized as a metal hydride to secure its long term storage. The recovered tritium will be made available for industrial uses and some research applications in the future. Then KEPRI is constructing the tritium lab. to build-up infrastructure to support tritium research activities and to support tritium control and accountability systems for tritium export. This paper describes the initial phases of the tritium application program including the laboratory infrastructure to support the tritium related R and D activities and the tritium controls in Korea

An open-walled ionization chamber appropriate to tritium monitoring for glovebox

International Nuclear Information System (INIS)

Chen Zhilin; Chang Ruiming; Mu Long; Song Guoyang; Wang Heyi; Wu Guanyin; Wei Xiye

2010-01-01

An open-walled ionization chamber is developed to monitor the tritium concentration in gloveboxes in tritium processing systems. Two open walls are used to replace the sealed wall in common ionization chambers, through which the tritium gas can diffuse into the chamber without the aid of pumps and pipelines. Some basic properties of the chamber are examined to evaluate its performance. Results turn out that an open-walled chamber of 1 l in volume shows a considerably flat plateau over 700 V for a range of tritium concentration. The chamber also gives a good linear response to gamma fields over 4 decades under a pressure condition of 1 atm. The pressure dependence characteristics show that the ionization current is only sensitive at low pressures. The pressure influence becomes weaker as the pressure increases mainly due to the decrease in the mean free path of β particles produced by tritium decay. The minimum detection limit of the chamber is 3.7x10 5 Bq/m 3 .

Stability of tritium permeation prevention barrier with TiC and TiN + TiC coating

International Nuclear Information System (INIS)

Shan Changqi; Chen Qingwang; Dai Shaoxia; Jiang Weisheng

1999-01-01

The stability of tritium permeation prevention barrier of 316L stainless steel with coating TiC and TiN + TiC under the conditions of very large thermal gradient, thermal cycling and plasma irradiation is researched. The research includes two aspects: one is the study on the stability resisting H + plasma irradiation; another is on the ability of two coating materials when they are used in long term under the condition of very large thermal gradient and cycling. The results show that TiC and TiN + TiC composite coating materials, after chemical heat treatment and forming tritium permeation prevention barrier, can resist H + ion irradiation, and also can resist very large thermal gradient and thermal cycling. The long time experiments show that tritium permeation prevention barrier of those coating materials is stable when they are used in long term

Recommendations for Tritium Science and Technology Research and Development in Support of the Tritium Readiness Campaign, TTP-7-084

Energy Technology Data Exchange (ETDEWEB)

Senor, David J. [Pacific Northwest National Lab. (PNNL), Richland, WA (United States)

2013-10-30

Between 2006 and 2012 the Tritium Readiness Campaign Development and Testing Program produced significant advances in the understanding of in-reactor TPBAR performance. Incorporating these data into existing TPBAR performance models has improved permeation predictions, and the discrepancy between predicted and observed tritium permeation in the WBN1 coolant has been decreased by about 30%. However, important differences between predicted and observed permeation still remain, and there are significant knowledge gaps that hinder the ability to reliably predict other aspects of TPBAR performance such as tritium distribution, component integrity, and performance margins. Based on recommendations from recent Tritium Readiness Campaign workshops and reviews coupled with technical and programmatic priorities, high-priority activities were identified to address knowledge gaps in the near- (3-5 year), middle- (5-10 year), and long-term (10+ year) time horizons. It is important to note that there are many aspects to a well-integrated research and development program. The intent is not to focus exclusively on one aspect or another, but to approach the program in a holistic fashion. Thus, in addition to small-scale tritium science studies, ex-reactor tritium technology experiments such as TMED, and large-scale in-reactor tritium technology experiments such as TMIST, a well-rounded research and development program must also include continued analysis of WBN1 performance data and post-irradiation examination of TPBARs and lead use assemblies to evaluate model improvements and compare separate-effects and integral component behavior.

Mean residence times for tritium in some terrestrial plants

International Nuclear Information System (INIS)

Gogate, S.S.; Krishnamoorthy, T.M.; Soman, S.D.

1975-01-01

Uptake of tritiated water from a single or multiple exposure, its fixation and elimination from 3 terrestrial plants, Raphanus sativus L., Amaranthus viridis L. and Phyllanthus fraternus Webster under experimental field conditions are described. Tissue free water tritium (TFWT) attains peak concentration within 4 hr after a single exposure in R. sativus and then decreases with a single component from both leaves and root, with a biological half-time of 36.4 +- 4.2 and 48.5 +- 7.2 hr respectively. TFWT in leaves of A. viridis reaches its peak value within 0.5 hr of exposure and its decay exhibits 2 component fall, one having a very short half-life of 2.4 +- 0.7 hr and the other a long half-time of 86.1 +- 2.0 hr. The two component decay of tritium in TFWT is well represented in P. fraternus. The long-lived components are nearly 8 times of the short-lived ones, both in leaves and stems respectively. Generally, the long -lived component accounts for 15% of the peak TFWT. Tissue bound tritium (TBT) reaches to 4% of TFWT in Phyllanthus sp. TBT elimination time is many times longer than the experimental periods employed in the present study. (author)

Evaluating All-Metal Valves for Use in a Tritium Environment

Energy Technology Data Exchange (ETDEWEB)

Houk, L. [Savannah River Site (SRS), Aiken, SC (United States). Savannah River National Lab. (SRNL); Payton, A. [Savannah River Site (SRS), Aiken, SC (United States). Savannah River National Lab. (SRNL)

2017-09-28

In the tritium gas processing system, it is desired to minimize polymer components due to their degradation from tritium exposure (beta decay). One source of polymers in the tritium process is valve components. A vendor has been identified that manufactures a valve that is marketed as being made from all-metal construction. This manufacturer, Ham-Let Group, manufactures a diaphragm valve (3LE series) that claims to be made entirely of metal. SRNL procured twelve (12) Ham-Let diaphragm valves for characterization and evaluation. The characterization tests include identification of the maximum pressure of these valves by performing pressure and burst tests. Leak tests were performed to ensure the valves do not exceed the acceptable leak rate for tritium service. These valves were then cycled in a nitrogen gas and/or vacuum environment to ensure they would be durable in a process environment. They were subsequently leak tested per ASTM protocol to ensure that the valves maintained their leak tight integrity. A detailed material analysis was also conducted to determine hydrogen and tritium compatibility.

Gamma irradiation, hot water and imazalil treatments on decay organisms and physical quality of stored netted muskmelon fruit

International Nuclear Information System (INIS)

Lester, G.

1989-01-01

Nonchemical treatments of gamma irradiation (2 Kilograys) and hot water (57°C) and the fungicide imazalil (1000 ppm) were compared with and without shrink-film wrap for effects on decay and physical quality of netted muskmelon fruit stored at 4°C for 0 through 60 days. Gamma irradiation was ineffective in controlling decay and surface molds, and injurious to physical quality by decreasing firmness, increasing fresh weight loss, membrane leakage and vein track browning. Hot water treatment coupled with shrink-film wrap was effective in controlling decay activity and maintaining physical quality up to 20 days storage. Imazalil coupled with shrink-film wrap controlled the incidence and severity of decay and maintained fruit firmness, moisture loss, membrane permeability and vein track browning for almost 60 days storage. (author)

Comparison of the effect of gamma irradiation, heat-radiation combination, and sulphur dioxide generating pads on decay and quality of grapes

International Nuclear Information System (INIS)

Thomas, Paul; Brij Bhushan; Joshi, M.R.

1995-01-01

Effect of gamma irradiation, heat-radiation combination and in-package sulphur dioxide fumigation on fungal decay, and quality of seedless grape cultivars, Thompson, Sonaka and Tas-A-Ganesh was evaluated under different storage regimes. Irradiation at 2 kGy or a combination of hot water dip (50 degC, 5 min), plus irradiation (1 kGy) showed less spoilage due to Rhizopus spp. and Botrytis spp. in grapes packaged in tissue paper lined boxes and stored at 4 deg, 15 deg and 25 degC. Storage in polyethylene lined boxes increased the fungal rot. In-package sulphur dioxide generating pad was most effective for control of decay in polyethylene lined boxes stored at 10 deg and 20 degC, but caused berry bleaching. Irradiation at 2.5 or 3.5 kGy controlled decay at 10 degC, but not so effectively at 20 degC. Organoleptic quality, berry firmness, and soluble solids were not affected by irradiation, but decreases in titratable acids and ascorbic acid were recorded. Packaging in polyethylene lined boxes retained berry turgidity, while slight shrivelling occurred in tissue paper lined boxes. The results indicate that gamma irradiation has potential as an alternative to sulphur dioxide fumigation for decay control during shipping and storage. (author). 20 refs., 4 tabs

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

Recovery of tritium from lithium-sintered aluminium product (SAP) and lithium-aluminium alloys

International Nuclear Information System (INIS)

Talbot, J.B.; Wiffen, F.W.

1979-01-01

The tritium release rates of irradiated samples of lithium-containing aluminium (Li-Al) and sintered aluminium product (Li-SAP) were investigated to evaluate the potential application of both materials in fusion reactors. The observed release rates followed the pattern expected for bulk diffusion of tritium in a solid. Therefore, diffusion coefficients for tritium in Li-SAP were determined over a temperature range of 383 and 500 0 C and tritium in Li-Al at 450 0 C. At 450 0 C, the diffusion coefficients of tritium in Li-SAP and Li-Al are 2.988 x 10 -10 cm 2 sec -1 and 1.462 x 10 -6 cm 2 sec -1 , respectively. (author)

Tritium calibration of the LUX dark matter experiment

Science.gov (United States)

Akerib, D. S.; Araújo, H. M.; Bai, X.; Bailey, A. J.; Balajthy, J.; Beltrame, P.; Bernard, E. P.; Bernstein, A.; Biesiadzinski, T. P.; Boulton, E. M.; Bradley, A.; Bramante, R.; Cahn, S. B.; Carmona-Benitez, M. C.; Chan, C.; Chapman, J. J.; Chiller, A. A.; Chiller, C.; Currie, A.; Cutter, J. E.; Davison, T. J. R.; de Viveiros, L.; Dobi, A.; Dobson, J. E. Y.; Druszkiewicz, E.; Edwards, B. N.; Faham, C. H.; Fiorucci, S.; Gaitskell, R. J.; Gehman, V. M.; Ghag, C.; Gibson, K. R.; Gilchriese, M. G. D.; Hall, C. R.; Hanhardt, M.; Haselschwardt, S. J.; Hertel, S. A.; Hogan, D. P.; Horn, M.; Huang, D. Q.; Ignarra, C. M.; Ihm, M.; Jacobsen, R. G.; Ji, W.; Kazkaz, K.; Khaitan, D.; Knoche, R.; Larsen, N. A.; Lee, C.; Lenardo, B. G.; Lesko, K. T.; Lindote, A.; Lopes, M. I.; Malling, D. C.; Manalaysay, A. G.; Mannino, R. L.; Marzioni, M. F.; McKinsey, D. N.; Mei, D.-M.; Mock, J.; Moongweluwan, M.; Morad, J. A.; Murphy, A. St. J.; Nehrkorn, C.; Nelson, H. N.; Neves, F.; O'Sullivan, K.; Oliver-Mallory, K. C.; Ott, R. A.; Palladino, K. J.; Pangilinan, M.; Pease, E. K.; Phelps, P.; Reichhart, L.; Rhyne, C.; Shaw, S.; Shutt, T. A.; Silva, C.; Solovov, V. N.; Sorensen, P.; Stephenson, S.; Sumner, T. J.; Szydagis, M.; Taylor, D. J.; Taylor, W.; Tennyson, B. P.; Terman, P. A.; Tiedt, D. R.; To, W. H.; Tripathi, M.; Tvrznikova, L.; Uvarov, S.; Verbus, J. R.; Webb, R. C.; White, J. T.; Whitis, T. J.; Witherell, M. S.; Wolfs, F. L. H.; Young, S. K.; Zhang, C.; LUX Collaboration

2016-04-01

We present measurements of the electron-recoil (ER) response of the LUX dark matter detector based upon 170 000 highly pure and spatially uniform tritium decays. We reconstruct the tritium energy spectrum using the combined energy model and find good agreement with expectations. We report the average charge and light yields of ER events in liquid xenon at 180 and 105 V /cm and compare the results to the NEST model. We also measure the mean charge recombination fraction and its fluctuations, and we investigate the location and width of the LUX ER band. These results provide input to a reanalysis of the LUX run 3 weakly interacting massive particle search.

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.

Tritium Removal by Laser Heating and Its Application to Tokamaks

International Nuclear Information System (INIS)

Skinner, C.H.; Gentile, C.A.; Guttadora, G.; Carpe, A.; Langish, S.; Young, K.M.; Nishi, M.; Shu, W.

2001-01-01

A novel laser heating technique has recently been applied to removing tritium from carbon tiles that had been exposed to deuterium-tritium (DT) plasmas in the Tokamak Test Fusion Reactor (TFTR). A continuous wave neodymium laser, of power up to 300 watts, was used to heat the surface of the tiles. The beam was focused to an intensity, typically 8 kW/cm 2 , and rapidly scanned over the tile surface by galvanometer-driven scanning mirrors. Under the laser irradiation, the surface temperature increased dramatically, and temperatures up to 2,300 degrees C were recorded by an optical pyrometer. Tritium was released and circulated in a closed-loop system to an ionization chamber that measured the tritium concentration. Most of the tritium (up to 84%) could be released by the laser scan. This technique appears promising for tritium removal in a next-step DT device as it avoids oxidation, the associated deconditioning of the plasma facing surfaces, and the expense of processing large quantities of tritium oxide. Some engineering aspects of the implementation of this method in a next-step fusion device will be discussed

Unclassified information on tritium extraction and purification technology: attachment 1

International Nuclear Information System (INIS)

McNorrill, P.L.

1976-01-01

Several tritium recovery and purification techniques developed at non-production sites are described in the unclassified and declassified literature. Heating of irradiated Li-Al alloy under vacuum to release tritium is described in declassified reports of Argonne National Laboratory. Use of palladium membranes to separate hydrogen isotopes from other gases is described by Argonne, KAPL, and others. Declassified KAPL reports describe tritium sorption on palladium beds and suggest fractional absorption as a means of isotope separation. A thermal diffusion column for tritium enrichment is described in a Canadian report. Mound Laboratory reports describe theoretical and experimental studies of thermal diffusion columns. Oak Ridge reports tabulate ''shape factors'' for thermal diffusion columns. Unclassified journals contain many articles on thermal diffusion theory, experiments, and separation of gas mixtures by thermal diffusion columns; much of these data can be readily extended to the separation of hydrogen-tritium mixtures. Cryogenic distillation for tritium recovery is described in the Mound Laboratory reports. Process equipment such as pumps, valves, Hopcalite beds, and uranium beds are described in reports by ANL, KAPL, and MLM, and in WASH-1269, Tritium Control Technology

Reactions of recoil tritium generated by the 3He(n,p)3H reaction with aromatic compounds -intramolecular tritium distribution and radiochemical yield

International Nuclear Information System (INIS)

Nogawa, N.; Morikawa, Naotake; Oohashi, Kunio; Matuoka, H.; Moki, T.; Moriya, T.

1986-01-01

Reactions of recoil tritium with benzoic acid, acetanilide and β-phenethyl alcohol were studied using the 3 He(=n,p) 3 H reaction. The tritium distribution in the aromatic ring is approximately uniform in all the irradiated compounds and the tritium activity per C-H bond in the methyl and ethylene groups is 7 to 8 relative to that of the corresponding ring as standard. These findings are substantially the same as those obtained previously by the 6 Li(n,α) 3 H reactions, suggesting the same mechanism of tritiation for both recoil reactions. The tritiated parent compounds were obtained in high radiochemical yields: 45% for benzoic acid, 30% for acetanilide, 12% for β-phenethyl alcohol. (author)

Evaluation of Tritium Behavior in the Epoxy Painted Concrete Wall of ITER Hot Cell

International Nuclear Information System (INIS)

Nakamura, Hirofumi; Hayashi, Takumi; Kobayashi, Kazuhiro; Nishi, Masataka

2005-01-01

Tritium behavior released in the ITER hot cell has been investigated numerically using a combined analytical methods of a tritium transport analysis in the multi-layer wall (concrete and epoxy paint) with the one dimensional diffusion model and a tritium concentration analysis in the hot cell with the complete mixing model by the ventilation. As the results, it is revealed that tritium concentration decay and permeation issues are not serious problem in a viewpoint of safety, since it is expected that tritium concentration in the hot cell decrease rapidly within several days just after removing the tritium release source, and tritium permeation through the epoxy painted concrete wall will be negligible as long as the averaged realistic diffusion coefficient is ensured in the concrete wall. It is also revealed that the epoxy paint on the concrete wall prevents the tritium inventory increase in the concrete wall greatly (two orders of magnitudes), but still, the inventory in the wall is estimated to reach about 0.1 PBq for 20 years operation

Tritium breeding experiments with lithium titanate in thermal-type mockups

International Nuclear Information System (INIS)

Klix, Axel; Takahashi, Akito; Ochiai, Kentaro; Nishitani, Takeo

2004-01-01

Lithium titanate, an advanced tritium breeding material, is currently investigated in integral mock-up experiments at FNS. A method was developed which allows to measure low tritium concentrations directly in this material. The local tritium production rate was obtained by small lithium titanate pellet detectors inserted into the breeding layers which are dissolved after irradiation of the assemblies, and the accumulated tritium was counted by liquid scintillation techniques. The measurement method was applied in mock0-up experiments with candidate materials for the future DEMO reactor breeding blanket. Experimental assemblies consisted of sheets of low activation ferritic steel F82H, lithium titanate, and berylium. Tritium production rate profiles were obtained and compared with results from calculations with the Monte Carlo neutron transport code MCNP-4C. In case of the mock-ups with 95% enriched lithium titanate, the C/E ratios were within the error estimate while larger discrepancies were observed in case of 40% enriched lithium titanate. (author)

Excretion of organic and inorganic tritiated compounds in cow's milk after ingestion of tritium oxide

International Nuclear Information System (INIS)

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

1980-01-01

The secretion of tritium in milk as water, casein and lipids was studied in cows given tritiated water to drink for 25 days. The parameters of the exponential functions describing the secretion of tritium as water, casein and lipid are determined during this 'loading phase' and also for a 'decay period' of 75 days after the tritiated water administration had been terminated. Secretion started after a short delay (0.5 day). Turnover of all three compounds was short (half time of about 5 days). Calculations of the dilution of the ingested water during metabolism showed that about 83% of the milk water secreted is found to originate from drinking water; the rest comes from water in food and from that formed in metabolism. The parameters of the decay phase indicated that the principle components of water, casein and lipids had about the same turnover rates as during the loading phase. Using the loading and decay phase data, calculations were performed to determine how much activity in each compound and in each metabolic component would be excreted after a single and after a continuous application of tritium oxide when integrated over infinite times. (UK)

Systematic preservation of teeth and prophylaxis of dental decay on irradiated patients. Preliminary results

Energy Technology Data Exchange (ETDEWEB)

Horiot, J C [Centre de Lutte contre le Cancer Georges-Francois-Leclerc, 21 - Dijon (France); Schraub, S [Centre Hospitalier Universitaire, 25 - Besancon (France)

1975-11-01

200 patients were irradiated on the oral cavity and on salivary glands with doses of 3,000 Rads and up. Teeth were preserved. A prophylactic treatment of dental decay was made using 5 minutes daily a fluoride gel into a carrier. The results showed an incidence of 5% for dental decay and 1% for osteo-radionecroses. Details are given about the selection of patients, the dental work-up and dental care before, during and after radiation therapy.

Design of an experiment to measure the decay heat of an irradiated PWR fuel: MERCI experiment; Conception d'une experience de mesure de la puissance residuelle d'un combustible irradie: l'experience MERCI

Energy Technology Data Exchange (ETDEWEB)

Bourganel, St

2002-11-01

After a reactor shutdown, a significant quantity of energy known as 'decay heat' continues to be generated from the irradiated fuel. This heat source is due to the disintegration energy of fission products and actinides. Decay heat determination of an irradiated fuel is of the utmost importance for safety analysis as the design cooling systems, spent fuel transport, or handling. Furthermore, the uncertainty on decay heat has a straight economic impact. The unloading fuel spent time is an example. The purpose of MERCI experiment (irradiated fuel decay heat measurement) consists in qualifying computer codes, particularly the DARWIN code system developed by the CEA in relation to industrial organizations, as EDF, FRAMATOME and COGEMA. To achieve this goal, a UOX fuel is irradiated in the vicinity of the OSIRIS research reactor, and then the decay heat is measured by using a calorimeter. The objective is to reduce the decay heat uncertainties from 8% to 3 or 4% at short cooling times. A full simulation on computer of the MERCI experiment has been achieved: fuel irradiation analysis is performed using transport code TRIPOLI4 and evolution code DARWIN/PEPIN2, and heat transfer with CASTEM2000 code. The results obtained are used for the design of this experiment. Moreover, we propose a calibration procedure decreasing the influence of uncertainty measurements and an interpretation method of the experimental results and evaluation of associated uncertainties. (author)

Tritium recycling and inventory in eroded debris of plasma-facing materials

International Nuclear Information System (INIS)

Hassanein, A.

1999-01-01

Damage to plasma-facing components (PFCs) and structural materials due to loss of plasma confinement in magnetic fusion reactors remains one of the most serious concerns for safe, successful, and reliable tokamak operation. High erosion losses due to surface vaporization, spallation, and melt-layer splashing are expected during such an event. The eroded debris and dust of the PFCs, including trapped tritium, will be contained on the walls or within the reactor chamber therefore, they can significantly influence plasma behavior and tritium inventory during subsequent operations. Tritium containment and behavior in PFCS and in the dust and debris is an important factor in evaluating and choosing the ideal plasma-facing materials (PFMs). Tritium buildup and release in the debris of candidate materials is influenced by the effect of material porosity on diffusion and retention processes. These processes have strong nonlinear behavior due to temperature, volubility, and existing trap sites. A realistic model must therefore account for the nonlinear and multidimensional effects of tritium diffusion in the porous-redeposited and neutron-irradiated materials. A tritium-transport computer model, TRAPS (Tritium Accumulation in Porous Structure), was developed and used to evaluate and predict the kinetics of tritium transport in porous media. This model is coupled with the TRICS (Tritium In Compound Systems) code that was developed to study the effect of surface erosion during normal and abnormal operations on tritium behavior in PFCS

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)

Tritium diffusion in polycrystalline lithium tungstate

International Nuclear Information System (INIS)

Krutyakov, A.N.; Shadrin, A.A.; Saunin, E.I.; Gromov, V.V.; Shafiev, A.I.

1984-01-01

Using radiometric method the investigation of tritium separation from neutron irradiated (neutron flux density 1.2x10 13 n/cm 2 xs) polycrystalline Li 2 WO 4 in the temperature range 200-680 deg C has been carried out. It is established that the use of helium as gas-carrier of flow-type gas-discharge counter permits to conduct continuous stable measurements of concentrations of tritium extracted depending on its chemical state. It is shown that volume diffusion is the process, limiting tritiated particle separation rate from Li 2 WO 4 . It is found that the process of tritium volume diffusion in Li 2 WO 4 corresponds to two different mechanisms respectively in low- (200-300 deg C) and high-temperature (350-680 deg C) ranges. A supposition is made that in the low-temperature range the process of diffusion is conditioned by the dissociation of the radiation defect-tritiated particle complex, which is confirmed by the data on radiation defect annealing in Li 2 WO 4 . The value of activation energy of tritium separation process in the range 350-680 deg C, proved to be equal to 13.3 kJ/mol. Possible role of crystal structure peculiarities of Li 2 WO 4 for diffusion process is pointed out

A basic study on the ITER tritium storage vessel design and components

International Nuclear Information System (INIS)

Chung, H. S.; Ahn, D. H.; Kim, K. R.; Yim, S. P.; Paek, S. W.; Lee, M. S.; Lee, S. H.; Shim, M. H.

2006-01-01

The ZrCo getter beds are built of a primary vessel which contains the ZrCo powder mixed with Cu spheres of less than one mm diameter and of a secondary outer vessel. The purpose of the secondary outer vessel is to capture permeated or leaked tritium and to present a good thermal insulation when properly evacuated. A third volume, a helium filled loop, is installed in the primary volume to remove the decay heat and is used to perform tritium accountancy measurements

Second international comparison on measuring techniques of tritium production rate for fusion neutronics experiments (ICMT-2)

International Nuclear Information System (INIS)

Maekawa, Fujio; Maekawa, Hiroshi

1993-02-01

An second international comparison on measuring techniques of tritium production rates for fusion neutronics experiments (ICMT-2) has been performed. The purpose is to evaluate the measurement accuracy of tritium production rates in the current measurement techniques. Two 14 MeV neutron source facilities, FNS at JAERI-Japan and LOTUS at EPFL-Switzerland, were used for this purpose. Nine groups out of seven countries participated in this program. A fusion simulated blanket assembly of simple-geometry was served as the test bed at each facility, in which Li-containing samples from the participants were irradiated in an uniform neutron field. The tritium production rates were determined by the participants using their own ways by using the liquid scintillation counting method. Tritiated water sample with unknown but the same concentration was also distributed and its concentration was measured to make a common reference. The standard deviation of measured tritium production rates among participants was about 10 % for both FNS and LOTUS irradiation levels: 4x10 -13 T-atoms/Li-atom and 1.6x10 -12 T-atoms/Li-atom at a sample, respectively. This standard deviation exceeds the expected deviation of 5 % in this program. It is presumed that the deviation of 10 % is caused mainly by the systematic and unknown errors in a process of tritium extraction from the irradiated samples depending on each organization. (author)

substantiation of the standards for tritium amino acids intake by human organism

International Nuclear Information System (INIS)

Zhesko, T.V.; Balonov, M.I.

1984-01-01

Calculated values of β-irradiation tissue doses of bound tritium and tritium oxide absorbed by animals treated with different amino acids are given. The obtained dose values are compared with tritium water doses. The data obtained in animal studies are extrapolated to man in order to determine the dose equivalent to the incorporated 3 H-amino acids dose. It is assumed that the dose equivalent to 3 H-amino acids radiation is three times as high as the equivalent amount of tritium oxide. 9 mCi/yr is established as the maximum allowable blood intake of 3 H-amino acids. Due to their metabolic characteristics, air permissible concentrations of 3 H-amino acids and tritium oxide have approximately the same values. The value of 30 nCi/cm 2 is recommended as a standard for work clothing contamination with 3 H-amino acids

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

Measurement of tritium production in 6LiD irradiated with neutrons from a critical system

International Nuclear Information System (INIS)

Duan Shaojie

1998-03-01

The tritium production rate and its distribution, in a 6 LiD semisphere on a critical assembly neutron source are measured with a 6 Li sandwich gold-silicon surface barrier detector. Then tritium production rate and the average tritium production length of the neutrons in the whole 6 LiD sphere are derived from approximate sphere symmetry

Tritium waste management on the La Hague AREVA NC site: associated impact and monitoring

International Nuclear Information System (INIS)

Devin, P.; Deguette, H.

2009-01-01

The authors propose an analysis of tritium behaviour in the nuclear fuel processed in the AREVA NC plant in La Hague, of its presence in the plant and in its wastes, and of the impact of these wastes and the tritium monitoring in the environment. First, they present the AREVA NC plant and evoke the legal context concerning the waste management. They report and discuss the analysis of the presence and behaviour of tritium in irradiated fuel, of its behaviour during spent fuel processing, the evolution of tritium releases (legal limitations, evolutions since 1992), of measurement of activity in effluents, and discuss a study of possible reductions of tritium releases by La Hague plants (mainly in sea waters). They also report the computational assessment of the dosimetric impact of tritium on neighbouring population. They describe how the presence of tritium in the environment is monitored within the annual radioactivity monitoring programme

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.

Tritium assay of Li2O pellets in the LBM/LOTUS experiments

International Nuclear Information System (INIS)

Quanci, J.; Azam, S.; Bertone, P.

1986-01-01

One of the objectives of the Lithium Blanket Module (LBM) program is to test the ability of advanced neutronics codes to model the tritium breeding characteristics of a fusion blanket exposed to a toroidal fusion neutron source. The LBM consists of over 20,000 cylindrical lithium oxide pellets and numerous diagnostic pellets and wafers. The LBM has been irradiated at the Ecole Polytechnique Federale de Lausanne (EPFL) LOTUS facility with a Haefely sealed neutron generator that gives a point deuterium-tritium neutron source up to 5 x 10 12 14-MeV n/s. Both Princeton Plasma Physics Lab. (PPPL) and EPFL assayed the tritium bred at various positions in the LBM. EPFL employed a dissolution technique while PPPL recovered the tritium by a thermal extraction method

Booster Long 13 irradiation studies

Energy Technology Data Exchange (ETDEWEB)

Leveling, A.; Mokhov, N.; Moore, C.D.; /Fermilab

1998-06-01

Extraction from the Booster to the Main Ring occurred at Long Straight 13. The nature of the extraction process was such that 1% to 2% of the beam was lost in this region. There was an appreciable amount of beam extracted as shown in Table 1, which gives the yearly integrated intensities from 1973 to 1997. A simple model of the extraction losses was set up by Chandra Bhat utilizing the program CASIM. A sample output I shown in figure 1 which gives contours of stars/cm3 in the dirt, also schematically depicted are the three six feet deep sampling holes which were drilled to map out this cascade. One aspect of this study has been the study of the production of non-migrating nuclides and further study may in fact yield better values for the K parameter, the probability per star that an atom of the particular nuclide will be produced. Also the results of this study can give experimental numbers for the production of other nuclides when the amount of Na22 has been calculated. However, the most important part of this study has been the determination of the amount of tritium produced by extraction from the Booster and the experimentally determined migration rate. If we look at the top sample result in hole S2 of 777 pCi/ml of tritium and use the experimentally determined rate of migration and the depth to the aquifer of 13.1m, they calculate that the concentration will have decayed away to 1.1E-8 pCi/ml. If we look at the bottom sample, which is 11.3 m away from the aquifer, they calculate that the 116 pCi/ml will have decayed to 5.2E-8 pCi/ml. The conclusions is that the rate of migration determined over the 24 year irradiation history of the Booster extraction point is small enough that there is no problem with migration of tritium to the aquifer.

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.

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

In situ measurement of tritium permeation through stainless steel

Energy Technology Data Exchange (ETDEWEB)

Luscher, Walter G., E-mail: walter.luscher@pnnl.gov [Pacific Northwest National Laboratory, 902 Battelle Blvd, Richland, WA 99352 (United States); Senor, David J., E-mail: david.senor@pnnl.gov [Pacific Northwest National Laboratory, 902 Battelle Blvd, Richland, WA 99352 (United States); Clayton, Kevin K., E-mail: kevin.clayton@inl.gov [Idaho National Laboratory, 2525 Fremont Ave., Idaho Falls, ID 83415 (United States); Longhurst, Glen R., E-mail: glenlonghurst@suu.edu [Idaho National Laboratory, 2525 Fremont Ave., Idaho Falls, ID 83415 (United States)

2013-06-15

Highlights: ► In situ tritium permeation measurements collected over broad pressure range. ► Test conditions relevant to 316 SS in commercial light water reactors. ► Comparisons between in- and ex-reactor measurements provided. ► Correlation between tritium permeation, temperature, and pressure developed. -- Abstract: 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 {sup 4}He carrier gas mixed with a specified quantity of tritium (T{sub 2}) 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 {sup 3}He to T, was also evaluated by introducing a {sup 4}He carrier gas mixed with {sup 3}He at a partial pressure of 1013 Pa at 330 °C. Less than 3% of the tritium resulting from {sup 3}He transmutation contributed to tritium permeation.

Response of E. coli Bsub(s-1) to tritium-. beta. particles under aerated and anoxic conditions

Energy Technology Data Exchange (ETDEWEB)

Lunec, J; Cramp, W A [Hammersmith Hospital, London (UK). M.R.C. Cyclotron Unit

1978-12-01

E.coli Bsub(s-1) cells were exposed to acute doses of tritium-..beta.. particles by suspension in tritiated water for known lengths of time. The resulting survival rate was compared with that obtained for external irradiation with 7 MeV electrons. The o.e.r. measured for tritium-..beta..s was not significantly different from the value of 2.15 measured for 7 MeV electrons. The r.b.e. of the tritium ..beta..s relative to 7 MeV electrons was 1.21 in both air and nitrogen. These results were compared with existing data for low voltage electron irradiations and with track segment studies of the effect of varying LET on the radiosensitivity of E.coli Bsub(s-1).

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.

The oxygen enhancement ratio for single- and double-strand breaks induced by tritium incorporated in DNA of cultured human T1 cells. Impact of the transmutation effect.

Science.gov (United States)

Tisljar-Lentulis, G; Henneberg, P; Feinendegen, L E; Commerford, S L

1983-04-01

The effect of oxygen, expressed as the oxygen enhancement ratio (OER), on the number of single-strand breaks (SSB) and double-strand breaks (DSB) induced in DNA by the radioactive decay of tritium was measured in human T1 cells whose DNA had been labeled with tritium at carbon atom number 6 of thymidine. Decays were accumulated in vivo under aerobic conditions at 0-1 degrees C and at -196 degrees C and in a nitrogen atmosphere at 0-1 degrees C. The number of SSB and DSB produced was analyzed by sucrose gradient centrifugation. For each tritium decay there were 0.25 DSB in cells exposed to air at 0-1 degrees C and 0.07 in cells kept under nitrogen, indicating an OER of 3.6, a value expected for such low-LET radiation. However, for each tritium decay there were 1.25 SSB in cells exposed to air at 0-1 degrees C and 0.76 in cells kept under nitrogen indicating an OER of only 1.7. The corresponding values for 60Co gamma radiation, expressed as SSB per 100 eV absorbed energy, were 4.5 and 1.0, giving an OER of 4.5. The low OER value found for SSB induced by tritium decay can be explained if 31% of the total SSB produced in air result from transmutation by a mechanism which does not produce DSB and is unaffected by oxygen.

Shipment and Storage Containers for Tritium Production Transportation Casks

International Nuclear Information System (INIS)

Massey, W.M.

1998-01-01

A shipping and storage container for the Tritium production transportation casks may be required but requirements for protection of the irradiated rods and radioactive contamination have not been finalized. This report documents the various possibilities for the container depending on the final requirements

An experiment to measure the electron neutrino mass using a cryogenic tritium source

International Nuclear Information System (INIS)

Fackler, O.; Jeziorski, B.; Kolos, W.; Monkhorst, H.; Mugge, M.; Sticker, H.; Szalewicz, K.; White, R.M.; Woerner, R.

1985-01-01

An experiment has been performed to determine the electron neutrino mass with the precision of a few eV by measuring the tritium beta decay energy distribution near the endpoint. Key features of the experiment are a 2 eV resolution electrostatic spectrometer and a high-activity frozen tritium source. It is important that the source have electronic wavefunctions which can be accurately calculated. These calculations have been made for tritium and the HeT + daughter ion and allow determination of branching fractions to 0.1% and energy of the excited states to 0.1 eV. The excited final molecular state calculations and the experimental apparatus are discussed. 4 refs., 5 figs

Post irradiation characterization of beryllium and beryllides after high temperature irradiation up to 3000 appm helium production in HIDOBE-01

Energy Technology Data Exchange (ETDEWEB)

Fedorov, A.V., E-mail: fedorov@nrg.eu [Nuclear Research and Consultancy Group, Westerduinweg 3, Postbus 25, Petten, 1755 ZG (Netherlands); Til, S. van; Stijkel, M.P. [Nuclear Research and Consultancy Group, Westerduinweg 3, Postbus 25, Petten, 1755 ZG (Netherlands); Nakamichi, M. [Japan Atomic Energy Agency, Rokkasho (Japan); Zmitko, M. [The European Joint Undertaking for ITER and the Development of Fusion Energy, c/ Josep Pla, n° 2, Torres Diagonal Litoral, Edificio B3, Barcelona 08019 (Spain)

2016-01-15

Titanium beryllides are considered as advanced candidate material for neutron multiplier for the helium cooled pebble bed (HCPB) and/or the water cooled ceramic breeder (WCCB) breeder blankets. In the HIDOBE-01 (HIgh DOse irradiation of BEryllium) experiment, beryllium and beryllide pellets with 5 at% and 7 at% Ti are irradiated at four different target temperatures (T{sub irr}): 425 °C, 525 °C, 650 °C and 750 °C up to the dose corresponding to 3000 appm He production in beryllium. The pellets were supplied by JAEA. During post irradiation examinations the critical properties of volumetric swelling and tritium retention were studied. Both titanium beryllide grades show significantly less swelling than the beryllium grade, with the difference increasing with the irradiation temperature. The irradiation induced swelling was studied by using direct dimensions. Both beryllide grades showed much less swelling as compare to the reference beryllium grade. Densities of the grades were studied by Archimedean immersion and by He-pycnometry, giving indications of porosity formation. While both beryllide grades show no significant reduction in density at all irradiation temperatures, the beryllium density falls steeply at higher T{sub irr}. Finally, the tritium release and retention were studied by temperature programmed desorption (TPD). Beryllium shows the same strong tritium retention as earlier observed in studies on beryllium pebbles, while the tritium inventory of the beryllides is significantly less, already at the lowest T{sub irr} of 425 °C.

MISTRAL: A comprehensive model for tritium transport in lithium-base ceramics. Pt. 2

International Nuclear Information System (INIS)

Federici, G.; Raffray, A.R.; Abdou, M.A.

1990-01-01

A new tritium transport model called MISTRAL (Model for Investigative Studies of Tritium Release in Lithium Ceramics) has been developed to describe and predict the kinetics of tritium release in lithium ceramic materials for tritium breeding applications in fusion blankets. The model has transient capabilities and has been developed to analyze the full range of transient conditions produced in in-pile tritium recovery experiments and expected in fusion blankets. Calibration of the model against experiments has been done in parallel with its development in order to assess its predictive capabilities and to identify the ranges of potential applicability. The comparisons of the results available for lithium metasilicate and aluminate samples irradiated respectively in the two in-pile tritium recovery experiments LISA1 and MOZART are presented and discussed in this paper. They have been selected for the calibration of the codes as being good examples of various features relevant for tritium release analysis in ceramic breeders under different transient conditions such as change in temperature, purge gas composition and reactor power. (orig.)

Simulating tritium retention in tungsten with a multiple trap model in the TMAP code

International Nuclear Information System (INIS)

Merrill, Brad J.; Shimada, Masashi; Humrickhouse, Paul W.

2013-01-01

Accurately predicting the quantity of tritium retained in plasma facing components is a key safety issue for licensing future fusion power reactors. Retention of tritium in the lattice damage caused when high energy neutrons collide with atoms in the structural material of the reactor's plasma facing components (PFCs) is an area of ongoing experimental research at the Idaho National Laboratory (INL) under the US/Japan TITAN collaboration. Recent experiments with the Tritium Plasma Experiment (TPE), located in the INL's Safety and Tritium Applied Research (STAR) facility, demonstrate that this damage can only be simulated by computer codes like the Tritium Migration Analysis Program (TMAP) if one assumes that the lattice damage produced by these neutrons results in multiple types of hydrogen traps (energy wells) within the material, each possessing a different trap energy and density. Previous attempts to simulate the quantity of deuterium released from neutron irradiated TPE tungsten targets indicated that at least six different traps are required by TMAP to model this release. In this paper we describe a recent extension of the TMAP trap site model to include as many traps as required by the user to simulate retention of tritium in neutron damaged tungsten. This model has been applied to data obtained for tungsten irradiated to a damage level of 0.025 dpa in the High Flux Isotope Reactor (HFIR) at the Oak Ridge National Laboratory (ORNL) after exposure to a plasma in TPE. (author)

Simultaneous measurement of tritium and radiocarbon by ultra-low-background proportional counting.

Science.gov (United States)

Mace, Emily; Aalseth, Craig; Alexander, Tom; Back, Henning; Day, Anthony; Hoppe, Eric; Keillor, Martin; Moran, Jim; Overman, Cory; Panisko, Mark; Seifert, Allen

2017-08-01

Use of ultra-low-background capabilities at Pacific Northwest National Laboratory provide enhanced sensitivity for measurement of low-activity sources of tritium and radiocarbon using proportional counters. Tritium levels are nearly back to pre-nuclear test backgrounds (~2-8 TU in rainwater), which can complicate their dual measurement with radiocarbon due to overlap in the beta decay spectra. We present results of single-isotope proportional counter measurements used to analyze a dual-isotope methane sample synthesized from ~120mg of H 2 O and present sensitivity results. Copyright © 2017 Elsevier Ltd. All rights reserved.

Autoradiographical Detection of Tritium in Cu-Ni Alloy by Scanning Electron Microscopy

OpenAIRE

高安, 紀; 中野, 美樹; 竹内, 豊三郎

1981-01-01

The autoradiograph of tritium dispersed in Cu-Ni alloy sheet by 6Li(n,α)3H reaction was obtained by a scanning electron microscope. Prior to the irradiation of neutrons 6Li was deposited on the sheet by evaporation. The liquid emulsion, Fuji-ER, was used in this study. The distribution of tritium was detected by the dispersion of silver grains remaining in the emulsion after the development was carried out.

Survey of tritium wastes and effluents in near-term fusion-research facilities

International Nuclear Information System (INIS)

Bickford, W.E.; Dingee, D.A.; Willingham, C.E.

1981-08-01

The use of tritium control technology in near-term research facilities has been studied for both the magnetic and inertial confinement fusion programs. This study focused on routine generation of tritium wastes and effluents, with little referene to accidents or facility decommissioning. This report serves as an independent review of the effectiveness of planned control technology and radiological hazards associated with operation. The facilities examined for the magnetic fusion program included Fusion Materials Irradiation Testing Facility (FMIT), Tritium Systems Test Assembly (TSTA), and Tokamak Fusion Test Reactor (TFTR) in the magnetic fusion program, while NOVA and Antares facilities were examined for the inertial confinement program

Results of tritium experiments on ceramic electrolysis cells and palladium diffusers for application to fusion reactor fuel cleanup systems

International Nuclear Information System (INIS)

Carlson, R.V.; Binning, K.E.; Konishi, S.; Yoshida, H.; Naruse, Y.

1987-01-01

Tritium tests at the Tritium Systems Test Assembly have demonstrated that ceramic electrolysis cells and palladium alloy diffuser developed in Japan are possible components for a fusion reactor fuel cleanup system. Both components have been successfully operated with tritium for over a year. A failure of the first electrolysis cell was most likely the result of an over voltage on the ceramic. A simple circuit was developed to eliminate this mode of failure. The palladium diffusers tubes exhibited some degradation of mechanical properties as a result of the build up of helium from the tritium decay, after 450 days of operation with tritium, however the effects were not significant enough to affect the performance. New models of the diffuser and electrolysis cell, providing higher flow rates and more tritium compatible designs are currently being tested with tritium. 8 refs., 5 figs

The response of E. coli Bsub(s-1) to tritium-β particles under aerated and anoxic conditions

International Nuclear Information System (INIS)

Lunec, J.; Cramp, W.A.

1978-01-01

E.coli Bsub(s-1) cells were exposed to acute doses of tritium-β particles by suspension in tritiated water for known lengths of time. The resulting survival rate was compared with that obtained for external irradiation with 7 MeV electrons. The o.e.r. measured for tritium-βs was not significantly different from the value of 2.15 measured for 7 MeV electrons. The r.b.e. of the tritium βs relative to 7 MeV electrons was 1.21 in both air and nitrogen. These results were compared with existing data for low voltage electron irradiations and with track segment studies of the effect of varying LET on the radiosensitivity of E.coli Bsub(s-1). (author)

Design of an experiment to measure the decay heat of an irradiated PWR fuel: MERCI experiment; Conception d'une experience de mesure de la puissance residuelle d'un combustible irradie: l'experience MERCI

Energy Technology Data Exchange (ETDEWEB)

Bourganel, St

2002-11-01

After a reactor shutdown, a significant quantity of energy known as 'decay heat' continues to be generated from the irradiated fuel. This heat source is due to the disintegration energy of fission products and actinides. Decay heat determination of an irradiated fuel is of the utmost importance for safety analysis as the design cooling systems, spent fuel transport, or handling. Furthermore, the uncertainty on decay heat has a straight economic impact. The unloading fuel spent time is an example. The purpose of MERCI experiment (irradiated fuel decay heat measurement) consists in qualifying computer codes, particularly the DARWIN code system developed by the CEA in relation to industrial organizations, as EDF, FRAMATOME and COGEMA. To achieve this goal, a UOX fuel is irradiated in the vicinity of the OSIRIS research reactor, and then the decay heat is measured by using a calorimeter. The objective is to reduce the decay heat uncertainties from 8% to 3 or 4% at short cooling times. A full simulation on computer of the MERCI experiment has been achieved: fuel irradiation analysis is performed using transport code TRIPOLI4 and evolution code DARWIN/PEPIN2, and heat transfer with CASTEM2000 code. The results obtained are used for the design of this experiment. Moreover, we propose a calibration procedure decreasing the influence of uncertainty measurements and an interpretation method of the experimental results and evaluation of associated uncertainties. (author)

Atomic effects in tritium beta-decay. II. Muon to electron conversion in atoms

International Nuclear Information System (INIS)

Wampler, K.D.

1989-01-01

I. The final-state, atomic effects in the low energy end of the tritium beta decay spectrum are studied in detail. The author treats the instantaneous, two-electron repulsion in the final state, effectively to all orders in perturbation theory, by solving the eigenvalue problem with a discretized and truncated form of the Hamiltonian. He finds that these effects fail to explain the distortion in the spectrum observed by Simpson (Phys. Rev. Lett. 54, 649 (1985)). Simpson attributed this distortion to the admixture of a heavy mass antineutrino in the outgoing electron antineutrino state. In fact, the final-state Coulomb effects enhance the distortion. This calculation clears up some of the ambiguities of other theoretical analyses based on considerations of screening functions and perturbation theory. II. He presents a phenomenological study of separate lepton number violating muon to electron conversion in atoms. Previous work on this process has concentrated on elastic transitions where the nucleus characteristics have the gate on the substrate and the source-drain contacts on the top of the sample. The first use as an FET dielectric is reported of hydrogenated amorphous silicon-carbon (prepared from silane and propane mixture), photo-oxidised by UV lamp or laser. These FETs have similar characteristics to those with silicon nitride gate insulator but without the difficulties of preparing good insulator/semiconductor interfaces. Using the same materials attempts have been made to produce charge coupled devices

Irradiaiton facilities for testing solid and liquid blanket breeder materials with in-situ tritium release measurements in the HFR Petten

International Nuclear Information System (INIS)

Conrad, R.; Debarberis, L.

1991-01-01

Lithium-based tritium breeder materials for solid and liquid fusion reactor blanket concepts are being tested in the High Flux Reactor (HFR) Petten with in-situ tritium release measurements since 1985, within the European Fusion Technology Programme and the BEATRIX-I programme. Ceramic breeder materials are being tested in the EXOTIC and COMPLIMENT experimental programmes and the liquid breeder material, Pb-17Li, is being tested in the LIBRETTO experimental programme. The in-pile experiments are performed with irradiation facilities developed by the Joint Research Centre (JRC) Petten. The irradiation vehicles are multi-channel rigs. The sample holders consist of independent, fully instrumented and triple contained capsules. The out-of-pile experimental equipment consist of twelve independent circuits for on-line tritium release and tritium permeation measurements and eight independent circuits for temperature control. The experimental achievements obtained so far contribute to the selection of candidate tritium breeder materials for blanket concepts of near future machines like NET, ITER and DEMO. (orig.)

Tritium release from lithium silicate and lithium aluminate, in-reactor and out-of-reactor

International Nuclear Information System (INIS)

Johnson, A.B. Jr.

1976-09-01

Studies were conducted to determine the generation and evolution of tritium and helium in lithium aluminate (LiAlO 2 ) and lithium silicate (Li 2 SiO 3 ) by the reaction: Li 6 + n → 4 He + T. Targets were irradiated 4.4 days in the K-West Reactor snout facility. (Silicate GVR* approximately 2.0 cc/cc; aluminate GVR approximately 1.4 cc/cc.) Gas release in-reactor was determined by post-irradiation drilling experiments on aluminum ampoules containing silicate and aluminate targets. In-reactor tritium release (at approximately 100 0 C) was found to decrease linearly with increasing target density. Tritium released in-reactor was primarily in the noncondensible form (HT and T 2 ), while in laboratory extractions (300-1300 0 C), the tritium appeared primarily in the condensible form (HTO and T 2 O). Concentrations of HT (and presumably HTO) were relatively high, indicating moisture pickup in canning operations or by inleakage of moisture after the capsule was welded. Impurities in extracted gases included H 2 O, CO 2 , CO, O 2 , H 2 , NO, SO 2 , SiF 4 and traces of hydrocarbons

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

Nondestructive post-irradiation examination of Loop-1, S1 and B1 rods

International Nuclear Information System (INIS)

Bratton, R.L.

1997-05-01

As a part of the Pacific Northwest National Laboratory's Tritium Target Development Program, eleven tritium target rods were irradiated in the Advanced Test Reactor located at the Idaho National Engineering and Environmental Laboratory during 1991. Both nondestructive and destructive post-irradiation examination on all eleven rods was planned under the Tritium Target Development Program. Funding for the program was reduced in 1991 resulting in the early removal of the program experiments before reaching their irradiation goals. Post-irradiation examination was only performed on one of the irradiated rods at the Pacific Northwest National Laboratory before the program was terminated in 1992. On December 6, 1995, the Secretary of Energy announced the pursuit of the Commercial Light-Water Reactor option for producing tritium establishing the Tritium Target Qualification Program at the Pacific Northwest National Laboratory. This program decided to pursue nondestructive and destructive post-irradiation examination of the ten remaining rods from the previous program. The ten rods comprise three experiments. The Loop-1 experiment irradiated eight target rods in a loop configuration for 217 irradiation days. The other two rods were irradiated in two separate irradiation experiments, designated as S1 and B1 for 143 effective full-power days, but at different power levels. After the ten rods were transferred from the ATR Canal to the Hot Fuels Examination Facility, the following examinations were performed: (1) visual examination and photography; (2) neutron radiography; (3) axial gamma scanning; (4) contact profilometry measurement; (5) bow and length measurements; (6) rod puncture and plenum gas analysis/measurement of plenum gas quantity; (7) void volume determination; and (8) internal pressure determination. This report presents the data collected during these examinations

Mechanical properties of irradiated beryllium

International Nuclear Information System (INIS)

Beeston, J.M.; Longhurst, G.R.; Wallace, R.S.

1992-01-01

Beryllium is planned for use as a neutron multiplier in the tritium breeding blanket of the International Thermonuclear Experimental Reactor (ITER). After fabricating samples of beryllium at densities varying from 80 to 100% of the theoretical density, we conducted a series of experiments to measure the effect of neutron irradiation on mechanical properties, especially strength and ductility. Samples were irradiated in the Advanced Test Reactor (ATR) to a neutron fluence of 2.6 x 10 25 n/m 2 (E > MeV) at an irradiation temperature of 75deg C. These samples were subsequently compression-tested at room temperature, and the results were compared with similar tests on unirradiated specimens. We found that the irradiation increased the strength by approximately four times and reduced the ductility to approximately one fourth. Failure was generally ductile, but the 80% dense irradiated samples failed in brittle fracture with significant generation of fine particles and release of small quantities of tritium. (orig.)

Mechanical properties of irradiated beryllium

Energy Technology Data Exchange (ETDEWEB)

Beeston, J.M.; Longhurst, G.R.; Wallace, R.S. (EG and G Idaho, Inc., Idaho Falls, ID (United States). Idaho National Engineering Lab.); Abeln, S.P. (EG and G Rocky Flats, Inc., Golden, CO (United States))

1992-10-01

Beryllium is planned for use as a neutron multiplier in the tritium breeding blanket of the International Thermonuclear Experimental Reactor (ITER). After fabricating samples of beryllium at densities varying from 80 to 100% of the theoretical density, we conducted a series of experiments to measure the effect of neutron irradiation on mechanical properties, especially strength and ductility. Samples were irradiated in the Advanced Test Reactor (ATR) to a neutron fluence of 2.6 x 10[sup 25] n/m[sup 2] (E > MeV) at an irradiation temperature of 75deg C. These samples were subsequently compression-tested at room temperature, and the results were compared with similar tests on unirradiated specimens. We found that the irradiation increased the strength by approximately four times and reduced the ductility to approximately one fourth. Failure was generally ductile, but the 80% dense irradiated samples failed in brittle fracture with significant generation of fine particles and release of small quantities of tritium. (orig.).

Mechanical properties of irradiated beryllium

Science.gov (United States)

Beeston, J. M.; Longhurst, G. R.; Wallace, R. S.; Abeln, S. P.

1992-10-01

Beryllium is planned for use as a neutron multiplier in the tritium breeding blanket of the International Thermonuclear Experimental Reactor (ITER). After fabricating samples of beryllium at densities varying from 80 to 100% of the theoretical density, we conducted a series of experiments to measure the effect of neutron irradiation on mechanical properties, especially strength and ductility. Samples were irradiated in the Advanced Test Reactor (ATR) to a neutron fluence of 2.6 × 10 25 n/m 2 ( E > 1 MeV) at an irradiation temperature of 75°C. These samples were subsequently compression-tested at room temperature, and the results were compared with similar tests on unirradiated specimens. We found that the irradiation increased the strength by approximately four times and reduced the ductility to approximately one fourth. Failure was generally ductile, but the 80% dense irradiated samples failed in brittle fracture with significant generation of fine particles and release of small quantities of tritium.

Remediation of ground water containing volatile organic compounds and tritium

International Nuclear Information System (INIS)

Shukla, S.N.; Folsom, E.N.

1994-03-01

The Trailer 5475 (T-5475) East Taxi Strip Area at Lawrence Livermore National Laboratory (LLNL), Livermore, California was used as a taxi strip by the US Navy to taxi airplanes to the runway from 1942 to 1947. Solvents were used in some unpaved areas adjacent to the East Taxi Strip for cleaning airplanes. From 1953 through 1976, the area was used to store and treat liquid waste. From 1962 to 1976 ponds were constructed and used for evaporation of liquid waste. As a result, the ground water in this area contains volatile organic compounds (VOCs) and tritium. The ground water in this area is also known to contain hexavalent chromium that is probably naturally occurring. Therefore, LLNL has proposed ''pump-and-treat'' technology above grade in a completely closed loop system. The facility will be designed to remove the VOCs and hexavalent chromium, if any, from the ground water, and the treated ground water containing tritium will be reinjected where it will decay naturally in the subsurface. Ground water containing tritium will be reinjected into areas with equal or higher tritium concentrations to comply with California regulations

Tritium solid targets for intense D-T neutron production and its related problems

International Nuclear Information System (INIS)

Sumita, Kenji

1988-01-01

This review paper is divided into three parts. Firstly, to attain an intense neutron production rate, the construction of a design with a higher tritium-containing surface and an effective cooling system like a rotating target device are discussed. The maximum attainable intensity based on tritium solid targets shall be estimated regarding planning for future D-T sources. Secondly, on the way to carry out some experiments, an absolute intensity calibration and an angular dependent neutron energy spectrum of the neutron source are essential parameters to analyse the results of the experiments. Sometimes the space dependent neutron spectrum is required as well as the space dependent neutron flux near the targets and irradiation samples. The measurement methods and their examples are reviewed for tritium solid targets. The third part is devoted to discuss the protection to tritium contamination problems due to unavoidable release of tritium gas from targets. Performance and effectiveness of tritium collection systems for intense D-T neutron sources shall be discussed in some examples. Tritium contamination incidents due to the faulted film powder of target surface are also reported in some real incident cases. (author). Abstract only

Final programmatic environmental impact statement for tritium supply and recycling. Volume III

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

Tritium in [18O]water containing [18F]fluoride for [18F]FDG synthesis

International Nuclear Information System (INIS)

Ito, Shigeki; Saze, Takuya; Sakane, Hitoshi; Ito, Satoshi; Ito, Shinichi; Nishizawa, Kunihide

2004-01-01

The presence of tritium in enriched [ 18 O]water irradiated with 9.6 MeV protons used to produce [ 18 F]fluoride by the 18 O(p, n) 18 F reaction was inferred from the cross sections and threshold energies of the 18 O(p, t) 16 O reaction, and the existence of tritium was confirmed experimentally. Tritium was also detected in both [ 18 O]water recovered for recycling and waste acetonitrile solutions. The purified [ 18 F]FDG was not contaminated with 3 H. The amount of 3 H discharged into the air was far less than the International Basic Safety Standard Level

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.)

Environmental monitoring for tritium in tritium separation facility

International Nuclear Information System (INIS)

Varlam, Carmen; Stefanescu, Ioan; Steflea, Dumitru; Lazar, Roxana Elena

2001-01-01

The Cryogenic Pilot is an experimental project in the nuclear energy national research program, which has the aim of developing technologies for tritium and deuterium separation by cryogenic distillation. The experimental installation is located 15 km near the highest city of the area and 1 km near Olt River. An important chemical activity is developed in the area and chemical plants make up almost entire neighborhood of the Experimental Cryogenic Pilot. It is necessary to emphasize this aspect because the hall sewage system of the pilot is connected with the one of other three chemical plants from vicinity. This is the reason why 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 sewage from neighboring industrial activity. In this work, a low background liquid scintillation was used to determine tritium activity concentration according to ISO 9698/1998 standard. We measured drinking water, precipitation, river water, underground water and wastewater. The tritium level was between 10 TU and 27 TU what indicates that there is no source of tritium contamination in the neighborhood of Cryogenic Pilot. In order to determine baseline levels we decided to monitor monthly each location. In this paper it is presented a standard method used for tritium determination in water samples, the precautions needed to achieve reliable results and the evolution of tritium level in different location near the Experimental Pilot for Tritium and Deuterium Cryogenic Separation. (authors)

Environmental monitoring for tritium at tritium separation facility

International Nuclear Information System (INIS)

Varlam, C.; Stefanescu, I.; Steflea, D.; Lazar, R.E.

2001-01-01

The Cryogenic Pilot is an experimental project in the nuclear energy national research program, which has the aim of developing technologies for tritium and deuterium separation by cryogenic distillation. The experimental installation is located 15 km near the highest city of the area and 1 km near Olt River. An important chemical activity is developed in the area and the Experimental Cryogenic Pilot's, almost the entire neighborhood are chemical plants. It is necessary to emphasize this aspect because the sewerage system is connected with the other three chemical plants from the neighborhood. This is the reason that 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 waste water of industrial activity from neighborhood. In this work, a low background liquid scintillation is used to determine tritium activity concentration according to ISO 9698/1998. We measured drinking water, precipitation, river water, underground water and waste water. The tritium level was between 10 TU and 27 TU that indicates there is no source of tritium contamination in the neighborhood of Cryogenic Pilot. In order to determine baseline levels we decide to monitories monthly each location. In this paper a standard method is presented which it is used for tritium determination in water sample, the precautions needed in order to achieve reliable results, and the evolution of tritium level in different location near the Experimental Pilot Tritium and Deuterium Cryogenic Separation.(author)

IN-SITU TRITIUM BETA DETECTOR

International Nuclear Information System (INIS)

Berthold, J.W.; Jeffers, L.A.

1998-01-01

The objectives of this three-phase project were to design, develop, and demonstrate a monitoring system capable of detecting and quantifying tritium in situ in ground and surface waters, and in water from effluent lines prior to discharge into public waterways. The tritium detection system design is based on measurement of the low energy beta radiation from the radioactive decay of tritium using a special form of scintillating optical fiber directly in contact with the water to be measured. The system consists of the immersible sensor module containing the optical fiber, and an electronics package, connected by an umbilical cable. The system can be permanently installed for routine water monitoring in wells or process or effluent lines, or can be moved from one location to another for survey use. The electronics will read out tritium activity directly in units of pico Curies per liter, with straightforward calibration. In Phase 1 of the project, we characterized the sensitivity of fluor-doped plastic optical fiber to tritium beta radiation. In addition, we characterized the performance of photomultiplier tubes needed for the system. In parallel with this work, we defined the functional requirements, target specifications, and system configuration for an in situ tritium beta detector that would use the fluor-doped fibers as primary sensors of tritium concentration in water. The major conclusions from the characterization work are: A polystyrene optical fiber with fluor dopant concentration of 2% gave best performance. This fiber had the highest dopant concentration of any fibers tested. Stability may be a problem. The fibers exposed to a 22-day soak in 120 F water experienced a 10x reduction in sensitivity. It is not known whether this was due to the build up of a deposit (a potentially reversible effect) or an irreversible process such as leaching of the scintillating dye. Based on the results achieved, it is premature to initiate Phase 2 and commit to a prototype

IN-SITU TRITIUM BETA DETECTOR

Energy Technology Data Exchange (ETDEWEB)

J.W. Berthold; L.A. Jeffers

1998-04-15

The objectives of this three-phase project were to design, develop, and demonstrate a monitoring system capable of detecting and quantifying tritium in situ in ground and surface waters, and in water from effluent lines prior to discharge into public waterways. The tritium detection system design is based on measurement of the low energy beta radiation from the radioactive decay of tritium using a special form of scintillating optical fiber directly in contact with the water to be measured. The system consists of the immersible sensor module containing the optical fiber, and an electronics package, connected by an umbilical cable. The system can be permanently installed for routine water monitoring in wells or process or effluent lines, or can be moved from one location to another for survey use. The electronics will read out tritium activity directly in units of pico Curies per liter, with straightforward calibration. In Phase 1 of the project, we characterized the sensitivity of fluor-doped plastic optical fiber to tritium beta radiation. In addition, we characterized the performance of photomultiplier tubes needed for the system. In parallel with this work, we defined the functional requirements, target specifications, and system configuration for an in situ tritium beta detector that would use the fluor-doped fibers as primary sensors of tritium concentration in water. The major conclusions from the characterization work are: A polystyrene optical fiber with fluor dopant concentration of 2% gave best performance. This fiber had the highest dopant concentration of any fibers tested. Stability may be a problem. The fibers exposed to a 22-day soak in 120 F water experienced a 10x reduction in sensitivity. It is not known whether this was due to the build up of a deposit (a potentially reversible effect) or an irreversible process such as leaching of the scintillating dye. Based on the results achieved, it is premature to initiate Phase 2 and commit to a prototype

Application of NaI(Tl) scintillation detector to measurement of tritium concentration

International Nuclear Information System (INIS)

Nishizawa, Kazushige; Endo, Yoshio; Shinagawa, Mutsuaki

1977-01-01

Measurements of tritium concentration in various media have been successfully performed by detecting with an ordinary NaI(Tl) scintillation counter the bremsstrahlung emitted from tritium decay. To distinguish meaningful signals from noises emanating mainly from thermoelectrons present in the phototube, differences in rise time were discriminated by means of an electronic circuit, instead of separation by pulse height analysis. This pulse-shape discriminator successfully reduced noise counts below 18 keV in a multichannel analyzer from 100 cpm to 4 cpm, which permitted direct counting of tritiated water as dilute as 1 μCi/ml, without requiring any complicated preparation. (auth.)

Simulation of tritium behavior after intended tritium release in ventilated room

International Nuclear Information System (INIS)

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

2001-01-01

At the Tritium Process Laboratory (TPL) at the 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 tritium behavior in the case where a tritium leak event 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 event should happen in a ventilated room. The RNG model was found to be valid for eddy flow calculation in the 50 m 3 /h ventilated Caisson with acceptable engineering precision. The calculated initial and removal tritium concentration histories after intended tritium release were consistent with the experimental observations in the 50 m 3 /h ventilated Caisson. It is found that the flow near a wall plays an important role for the tritium transport in the ventilated room. On the other hand, tritium behavior intentionally released in the 3,000 m 3 of tritium handling room was investigated experimentally under a US-Japan collaboration. The tritium concentration history calculated with the same method was consistent with the experimental observations, which proves that the present developed method can be applied to the actual scale of tritium handling room. (author)

Tritium labeling by thermally generated tritons

International Nuclear Information System (INIS)

Morimoto, H.; Williams, P.G.; Saljoughian, M.

1988-06-01

The predominant effect of thermal atom irradiation on solid molecules is saturation of their aromatic functions. Only low level of tritium exchange is observed for aliphatic solids. In contrast, liquids whose frozen surface can be rendered somewhat mobile at appropriate temperatures exhibit more exchange than addition. The rank order of effectiveness of several metals in promoting exchange/addition appears similar to the rank order for heterogeneous catalytic hydrogenation. 3 refs., 8 figs

A laboratory information management system for the analysis of tritium (3H) in environmental waters.

Science.gov (United States)

Belachew, Dagnachew Legesse; Terzer-Wassmuth, Stefan; Wassenaar, Leonard I; Klaus, Philipp M; Copia, Lorenzo; Araguás, Luis J Araguás; Aggarwal, Pradeep

2018-07-01

Accurate and precise measurements of low levels of tritium ( 3 H) in environmental waters are difficult to attain due to complex steps of sample preparation, electrolytic enrichment, liquid scintillation decay counting, and extensive data processing. We present a Microsoft Access™ relational database application, TRIMS (Tritium Information Management System) to assist with sample and data processing of tritium analysis by managing the processes from sample registration and analysis to reporting and archiving. A complete uncertainty propagation algorithm ensures tritium results are reported with robust uncertainty metrics. TRIMS will help to increase laboratory productivity and improve the accuracy and precision of 3 H assays. The software supports several enrichment protocols and LSC counter types. TRIMS is available for download at no cost from the IAEA at www.iaea.org/water. Copyright © 2018 Elsevier Ltd. All rights reserved.

Overview of R and D activities on tritium processing and handling technology in JAEA

Energy Technology Data Exchange (ETDEWEB)

Yamanishi, Toshihiko, E-mail: yamanishi.toshihiko@jaea.go.jp [Japan Atomic Energy Agency, Tokai, Ibaraki 319-1195 (Japan); Nakamura, Hirofumi; Kawamura, Yoshinori; Iwai, Yasunori; Isobe, Kanetsugu; Oyaidsu, Makoto; Yamada, Masayuki; Suzuki, Takumi; Hayashi, Takumi [Japan Atomic Energy Agency, Tokai, Ibaraki 319-1195 (Japan)

2012-08-15

Highlights: Black-Right-Pointing-Pointer The tritium technologies have been studied at Tritium Process Laboratory of JAEA. Black-Right-Pointing-Pointer A monitoring method for the blanket system of a fusion reactor have been studied. Black-Right-Pointing-Pointer Basic studies on the tritium behavior in confinement system have been carried out. Black-Right-Pointing-Pointer Studies on the detritiation have been carried out as another significant activity. - Abstract: In JAEA, the tritium processing and handling technologies have been studied at TPL (Tritium Process Laboratory). The main R and D activities are: the tritium processing technology for the blanket recovery systems; the basic tritium behavior in confinement materials; and detritiation and decontamination. The R and D activities on tritium processing and handling technologies for a demonstration reactor (DEMO) are also planned to be carried out in the broader approach (BA) program by JAEA with Japanese universities. The ceramic proton conductor has been studied as a possible tritium processing method for the blanket system. The BIXS method has also been studied as a monitoring of tritium in the blanket system. The hydrogen transfer behavior from water to metal has been studied as a function of temperature. As for the behavior of high concentration tritium water, it was observed that the formation of the oxidized layer was prevented by the presence of tritium in water (0.23 GBq/cc). A new hydrophobic catalyst has been developed for the conversion of tritium to water. The catalyst could convert tritium to water at room temperature. A new Nafion membrane has also been developed by gamma ray irradiation to get the strong durability for tritium.

Potential role of the Fast Flux Test Facility and the advanced test reactor in the U.S. tritium production system

International Nuclear Information System (INIS)

Dautel, W.A.

1996-01-01

The Department of Energy is currently engaged in a dual-track strategy to develop an accelerator and a commercial light water reactor (CLWR) as potential sources of tritium supply. New analysis of the production capabilities of the Fast Flux Test Facility (FFTF) at the Hanford Site argues for considering its inclusion in the tritium supply,system. The use of the FFTF (alone or together with the Advanced Test Reactor [ATR] at the Idaho National Engineering Laboratory) as an integral part of,a tritium production system would help (1) ensure supply by 2005, (2) provide additional time to resolve institutional and technical issues associated with the- dual-track strategy, and (3) reduce discounted total life-cycle'costs and near-tenn annual expenditures for accelerator-based systems. The FFRF would also provide a way to get an early start.on dispositioning surplus weapons-usable plutonium as well as provide a source of medical isotopes. Challenges Associated With the Dual-Track Strategy The Department's purchase of either a commercial reactor or reactor irradiation services faces challenging institutional issues associated with converting civilian reactors to defense uses. In addition, while the technical capabilities of the individual components of the accelerator have been proven, the entire system needs to be demonstrated and scaled upward to ensure that the components work together 1548 as a complete production system. These challenges create uncertainty over the ability of the du2a-track strategy to provide an assured tritium supply source by 2005. Because the earliest the accelerator could come on line is 2007, it would have to operate at maximum capacity for the first few years to regenerate the reserves lost through radioactive decay after 2005

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)

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.)

LIBRETTO-3: modelling tritium extraction/permeation and evaluation of permeation barriers under irradiation

International Nuclear Information System (INIS)

Sedano, L.A.; Fuetterer, M.A.; Viola, R.; Dies, X.

1996-01-01

Permeation barriers are required in order to limit the size and cost of the detritiation plants for future fusion reactor blankets of the water-cooled Pb-17Li type. The LIBRETTO irradiations were performed to evaluate the efficiency of permeation barriers under high flux reactor (HFR) conditions. Tritium extraction and permeation characteristics from Pb-17Li under variable temperatures 553-723 K, H 2 doping (0-1 vol%) and purge gas flow rates 20-100 scc/min were tested in LIBRETTO-3. An external TiC coating, an internal (TiC+Al 2 O 3 ), both produced by chemical vapour deposition (CVD), and an internal Al 2 O 3 produced by pack cementation (PC) on AISI 316L steel were tested as permeation barriers. The release mechanisms, experimental uncertainties and method for permeation barriers qualification are presented. As a result permeation reduction factors (PRF) at 0.1 dpa of 17 and 34 were obtained for the CVD-Al 2 O 3 at 498 K and for the PC-Al 2 O 3 at 508 K, respectively. These values were confirmed by a residence time analysis and are higher than in a preliminary analysis. (orig.)

Tritium release from lithium silicate and lithium aluminate, in-reactor and out-of-reactor

Energy Technology Data Exchange (ETDEWEB)

Johnson, A.B. Jr.

1976-09-01

Studies were conducted to determine the generation and evolution of tritium and helium in lithium aluminate (LiAlO/sub 2/) and lithium silicate (Li/sub 2/SiO/sub 3/) by the reaction: Li/sup 6/ + n ..-->.. /sup 4/He + T. Targets were irradiated 4.4 days in the K-West Reactor snout facility. (Silicate GVR* approximately 2.0 cc/cc; aluminate GVR approximately 1.4 cc/cc.) Gas release in-reactor was determined by post-irradiation drilling experiments on aluminum ampoules containing silicate and aluminate targets. In-reactor tritium release (at approximately 100/sup 0/C) was found to decrease linearly with increasing target density. Tritium released in-reactor was primarily in the noncondensible form (HT and T/sub 2/), while in laboratory extractions (300-1300/sup 0/C), the tritium appeared primarily in the condensible form (HTO and T/sub 2/O). Concentrations of HT (and presumably HTO) were relatively high, indicating moisture pickup in canning operations or by inleakage of moisture after the capsule was welded. Impurities in extracted gases included H/sub 2/O, CO/sub 2/, CO, O/sub 2/, H/sub 2/, NO, SO/sub 2/, SiF/sub 4/ and traces of hydrocarbons.

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)

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)

Recovery of tritium from CANDU reactors, its storage and monitoring of its migration in the environment

International Nuclear Information System (INIS)

Holtslander, W.J.; Osborne, R.V.

1979-07-01

Tritium is produced in CANDU heavy water reactors mainly by neutron activation of deuterium. The typical production rate is 2.4 kCi per megawatt-year (89 TBq. per megawatt-year. In Pickering Generating Station the average concentration of tritium in the moderators has reached 16 Ci.kg -1 (0.6 TBq.kg -1 ) and in coolants, 0.5 Ci.kg -1 (0.02 TBq.kg -1 ). Concentrations will continue to increase towards an equilibrium determined by the production rate, the tritium decay rate and heavy water replacement. Tritium removal methods that are being considered for a pilot plant design are catalytic exchange of DTO with D 2 and electrolysis of D 2 O/DTO to provide feed for cryogenic distillation of D 2 /DT/T 2 . Storage methods for the removed tritium - as elemental gas, as metal hydrides and in cements - are also being investigated. Transport of tritiated wastes should not be a particularly difficult problem in light of extensive experience in transporting tritiated heavy water. Methods for determining the presence of tritium in the environment of any tritium handling facility are well established and have the capability of measuring concentrations of tritium down to current ambient values. (author)

Helium-3 mass spectrometry for low-level tritium analysis of environmental samples

International Nuclear Information System (INIS)

Surano, K.A.; Hudson, G.B.; Failor, R.A.; Sims, J.M.; Holland, R.C.; MacLean, S.C.; Garrison, J.C.

1991-04-01

Helium-3 ( 3 He) mass spectrometry for the analysis of low-level tritium ( 3 H) concentrations in environmental sample matrices was compared with conventional low-level β-decay counting methods. The mass-spectrometry method compared favorably, equaling or surpassing conventional decay-counting methods with respect to most criteria. Additional research and method refinements may make 3 He mass spectrometry the method of choice for routine, low-level to very-low-level 3 H measurements in a wide variety of environmental samples in the future

Final programmatic environmental impact statement for tritium supply and recycling. Volume 1

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. 550 refs

Reducing the tritium inventory in waste produced by fusion devices

Energy Technology Data Exchange (ETDEWEB)

Pamela, J., E-mail: jerome.pamela@cea.fr [CEA, Agence ITER-France, F-13108 Saint-Paul-lez-Durance (France); Decanis, C. [CEA, DEN, Centre de Cadarache, F-13108 Saint-Paul-lez-Durance (France); Canas, D. [CEA, DEN/DADN, Centre de Saclay, F-91191 Gif-sur-Yvette cedex (France); Liger, K.; Gaune, F. [CEA, DEN, Centre de Cadarache, F-13108 Saint-Paul-lez-Durance (France)

2015-04-15

Highlights: • Fusion devices including ITER will generate tritiated waste, some of which will need to be detritiated before disposal. • Interim storage is the reference solution offering an answer for all types of tritiated radwaste. • Incineration is very attractive for VLLW and possibly SL-LILW soft housekeeping waste, since it offers higher tritium and waste volume reduction than the alternative thermal treatment technique. • For metallic waste, further R&D efforts should be made to optimize tritium release management and minimize the need for interim storage. - Abstract: The specific issues raised by tritiated waste resulting from fusion machines are described. Of the several categories of tritium contaminated waste produced during the entire lifespan of a fusion facility, i.e. operating phase and dismantling phase, only two categories are considered here: metal components and solid combustible waste, especially soft housekeeping materials. Some of these are expected to contain a high level of tritium, and may therefore need to be processed using a detritiation technique before disposal or interim storage. The reference solution for tritiated waste management in France is a 50-year temporary storage for tritium decay, with options for reducing the tritium content as alternatives or complement. An overview of the strategic issues related to tritium reduction techniques is proposed for each radiological category of waste for both metallic and soft housekeeping waste. For this latter category, several options of detritiation techniques by thermal treatment like heating up or incineration are described. A comparison has been made between these various technical options based on several criteria: environment, safety, technical feasibility and costs. For soft housekeeping waste, incineration is very attractive for VLLW and possibly SL-LILW. For metallic waste, further R&D efforts should be conducted.

Phase 1 Final Report for In-Situ Tritium Beta Detector

Energy Technology Data Exchange (ETDEWEB)

Berthold, J.W.; Jeffers, L.A.

1998-04-15

The objectives of this three-phase project were to design, develop, and demonstrate a monitoring system capable of detecting and quantifying tritium in situ in ground and surface waters, and in water from effluent lines prior to discharge into public waterways. The tritium detection system design is based on measurement of the low energy beta radiation from the radioactive decay of tritium using a special form of scintillating optical fiber directly in contact with the water to be measured. The system consists of the immersible sensor module containing the optical fiber, and an electronics package, connected by an umbilical cable. The system can be permanently installed for routine water monitoring in wells or process or effluent lines, or can be moved from one location to another for survey use. The electronics will read out tritium activity directly in units of pico Curies per liter, with straightforward calibration. In Phase 1 of the project, we characterized the sensitivity of fluor-doped plastic optical fiber to tritium beta radiation. In addition, we characterized the performance of photomultiplier tubes needed for the system. In parallel with this work, we defined the functional requirements, target specifications, and system configuration for an in situ tritium beta detector that would use the fluor-doped fibers as primary sensors of tritium concentration in water. The major conclusions from the characterization work are: A polystyrene optical fiber with fluor dopant concentration of 2% gave best performance. This fiber had the highest dopant concentration of any fibers tested. Stability may be a problem. The fibers exposed to a 22-day soak in 120 F water experienced a 10x reduction in sensitivity. It is not known whether this was due to the build up of a deposit (a potentially reversible effect) or an irreversible process such as leaching of the scintillating dye.

Experimental study of the tritium inventory in the BR3 and extrapolation to a P.W.R. of 900 MWe

International Nuclear Information System (INIS)

Charlier, A.; Gubel, P.; Vandenberg, C.; Haas, D.

1982-01-01

The aim of this report is to evaluate the tritium production and diffusion in uranium and plutonium fuel in the primary circuit of a PWR and to improve the knowledge about the production difference between the two kinds of isotopes. The first part of the work is relative to the experimental PWR BR3, cycle 4A, during which a constant control of the tritium activity has been performed in the primary circuit. These experimental evaluation was compared with the the theoretical estimation of the tritium production during the cycle 4A. From these observations and calculations, a tritium release fraction was deduced and estimated to be 0.81% of the total tritium produced in the fuel. The second part of the work is devoted to post-irradiation examinations on a few uranium and plutonium rods irradiated in the BR3 reactor. The tritium content was measured in the cladding, in the fuel and in the gas plenum for various samples of fuel rods. These results show the relationship between the release rate from the fuel matrix, the linear power and the burnup. The last part of the work is the estimate of the tritium production in a PWR of 900 MWe in operating conditions. The tritium production was calculated for an uranium fuelled core and for a core containing 30% of all plutonium fuel assemblies in a generic power plant of 900 MWe. From this study, it results that the loading with 30% plutonium assemblies at equilibrium increases the tritium balance in the moderator water of less than 5%

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)

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)

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

Joint research centre fusion materials irradiations in HFR: Present status and prospectives

International Nuclear Information System (INIS)

Casini, G.; Fenici, P.

1989-01-01

First a review is made of the Joint Research Centre experimental activity at HFR-Petten in the frame of the Fusion Technology and Safety Programme. The materials under investigation are: Cr-Ni Austenitic steels (316-L type) and Cr-Mn Austenitic steels (AMCR and FI type) as structural materials and Pb-17Li eutetic as tritium breeding material. The experiments on structural materials comprise: Sample irradiations with post-irradiation tensile tests (FRUST) Sample irradiations under constant load and post-irradiation strain measurement (TRIESTE) On-line creep tests (CRISP). The experiments on Pb-17Li breeder material regard sample irradiations to investigate tritium production and recovery as well as tritium permeation through blanket structures (LIBRETTO Experiment). Both irradiations on structural and breeding materials will be pursued up to the end of the current JRC-Multiannual Programme (1988-1991) and even further. In the last part of the paper expected developments of the testing programme at HFR are discussed. New areas of research should involve materials for divertor applications (NET/ITER) and advanced low activation composite materials for Commercial Power Reactors

Study on neutron irradiation behavior of beryllium as neutron multiplier

Energy Technology Data Exchange (ETDEWEB)

Ishitsuka, Etsuo [Japan Atomic Energy Research Inst., Oarai, Ibaraki (Japan). Oarai Research Establishment

1998-03-01

More than 300 tons beryllium is expected to be used as a neutron multiplier in ITER, and study on the neutron irradiation behavior of beryllium as the neutron multiplier with Japan Materials Testing Reactor (JMTR) were performed to get the engineering data for fusion blanket design. This study started as the study on the tritium behavior in beryllium neutron reflector in order to make clear the generation mechanism on tritium of JMTR primary coolant since 1985. These experiences were handed over to beryllium studies for fusion study, and overall studies such as production technology of beryllium pebbles, irradiation behavior evaluation and reprocessing technology have been started since 1990. In this presentation, study on the neutron irradiation behavior of beryllium as the neutron multiplier with JMTR was reviewed from the point of tritium release, thermal properties, mechanical properties and reprocessing technology. (author)

Tritium breeders and tritium permeation barrier coatings for fusion reactor

International Nuclear Information System (INIS)

Yamawaki, Michio; Kawamura, Hiroshi; Tsuchiya, Kunihiko

2004-01-01

A state of R and D of tritium breeders and tritium permeation barrier coatings for fusion reactor is explained. A list of candidate for tritium breeders consists of ceramics containing lithium, for examples, Li 2 O, Li 2 TiO 3 , Li 2 ZrO 3 , Li 4 SiO 4 and LiAlO 2 . The characteristics and form are described. The optimum particle size is from 1 to 10 μm. The production technologies of tritium breeders in the world are stated. Characteristics of ceramics with lithium as tritium breeders are compared. TiC, TiN/TiC, Al 2 O 3 and Cr 2 O 3 -SiO 2 -P 2 O 5 are tritium permeation barrier coating materials. These production methods and evaluation of characteristics are explained. (S.Y.)

Experimental investigation on tritium release from lithium titanate pebble under high temperature of 1073 K

Energy Technology Data Exchange (ETDEWEB)

Ochiai, Kentaro, E-mail: howartre@onid.oregonstate.edu [Japan Atomic Energy Agency, Tokai-mura, Naka-gun, Ibaraki (Japan); Edao, Yuki; Kawamura, Yoshinori [Japan Atomic Energy Agency, Tokai-mura, Naka-gun, Ibaraki (Japan); Hoshino, Tsuyoshi [Japan Atomic Energy Agency, Rokkasho-mura, Kamikita-gun, Aomori (Japan); Ohta, Masayuki; Sato, Satoshi; Konno, Chikara [Japan Atomic Energy Agency, Tokai-mura, Naka-gun, Ibaraki (Japan)

2015-10-15

Highlights: • We have performed the tritium recovery experiment with the DT neutron source at 1073 K. • The tritium recovery corresponded with the calculated tritium production. • The chemical form of recovered tritium is affected by the temperature and kind of sweep gas. • The recovered HT increases at higher temperature and dry hydrogen circumstance. - Abstract: The temperature of Li{sub 2}TiO{sub 3} pebble breeder in a fusion DEMO blanket is assumed to be more than 1000 K. For the investigation of tritium release from a Li{sub 2}TiO{sub 3} pebble breeder blanket at such a high temperature, we have carried out a tritium release experiment with the DT neutron source at the JAEA-FNS. The Li{sub 2}TiO{sub 3} pebble (1.0–1.2 mm in diameter) of 70 g was put into a stainless steel container and installed into an assembly stratified with beryllium and Li{sub 2}TiO{sub 3} layers. During the DT neutron irradiation, the temperature was kept at 1073 K with wire heaters in the blanket container. Helium gas including 1% hydrogen gas (H{sub 2}/He) mainly flowed inside the container as the purge gas. Two chemical forms, HT and HTO, of extracted tritium were separately collected during the DT neutron irradiation by using water bubblers and CuO bed. The tritium activity in the water bubbler was measured by a liquid scintillation counter. To investigate the effect of moisture in the purge gas, we also performed the same experiments with H{sub 2}O/He gas (H{sub 2}O content: 1%) or pure helium gas. From our experiment at 1073 K, in the case of the purge gas includes H{sub 2}, it is indicated that the increasing tendency of HT release is similar to that of the dry H{sub 2}/He.

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

Quality Control Samples for the Radiological Determination of Tritium in Urine Samples

International Nuclear Information System (INIS)

Ost'pezuk, P.; Froning, M.; Laumen, S.; Richert, I.; Hill, P.

2004-01-01

The radioactive decay product of tritium is a low energy beta that cannot penetrate the outer dead layer of human skin. Therefore , the main hazard associated with tritium is internal exposure. In addition, due to the relatively long half life and short biological half life, tritium must be ingested in large amounts to pose a significant health risk. On the other hand, the internal exposure should be kept as low as practical. For incorporation monitoring of professional radiation workers the quality control is of utmost importance. In the Research Centre Juelich GmbH (FZJ) a considerable fraction of monitoring by excretion analysis relates to the isotope Tritium. Usually an aliquot of an urine sample is mixed with a liquid scintillator and measured in a liquid scintillation counter. Quality control samples in the form of three kind of internal reference samples (blank, reference samples with low activity and reference sample with elevated activity) were prepared from a mixed, Tritium (free) urine samples. 1 ml of these samples were pipetted into a liquid scintillation vial. In the part of theses vials a known amounts of Tritium were added. All these samples were stored at 20 degrees. Based on long term use of all these reference samples it was possible to construct appropriate control charts with the upper and lower alarm limits. Daily use of these reference samples decrease significantly the risk for false results in original urine with no significant increase of the determination time. (Author) 2 refs

Studies on chemical phenomena of high concentration tritium water and organic compounds of tritium from viewpoint of the tritium confinement

International Nuclear Information System (INIS)

Yamanishi, Toshihiko; Hayashi, Takumi; Iwai, Yasunori; Isobe, Kanetsugu; Hara, Masanori; Sugiyama, Takahiko; Okuno, Kenji

2009-01-01

As a part of the grant-in-aid for scientific research on priority areas entitled 'frontiers of tritium researches toward fusion reactors', coordinated two research programs on chemical phenomena of high concentration tritium water and organic compounds of tritium from view point of the tritium confinement have been conducted by the C01 team. The results are summarized as follows: (1) Chemical effects of the high concentration tritium water on stainless steels as structural materials of fusion reactors were investigated. Basic data on tritium behaviors at the metal-water interface and corrosion of metal in tritium water were obtained. (2) Development of the tritium confinement and extraction system for the circulating cooling water in the fusion reactor was studied. Improvement was obtained in the performance of a chemical exchange column and catalysts as major components of the water processing system. (J.P.N.)

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

Radiation durability of polymeric materials in solid polymer electrolyzer for fusion tritium plant

International Nuclear Information System (INIS)

Iwai, Yasunori; Yamanishi, Toshihiko; Hiroki, Akihiro; Tamada, Masao

2009-02-01

This document presents the radiation durability of various polymeric materials applicable to a solid-polymer-electrolyte (SPE) water electrolyzer to be used in the tritium facility of fusion reactor. The SPE water electrolyzers are applied to the water detritiation system (WDS) of the ITER. In the ITER, an electrolyzer should keep its performance during two years operation in the tritiated water of 9TBq/kg, the design tritium concentration of the ITER. The tritium exposure of 9TBq/kg for two years is corresponding to the irradiation of no less than 530 kGy. In this study, the polymeric materials were irradiated with γ-rays or with electron beams at various conditions up to 1600 kGy at room temperature or at 343 K. The change in mechanical and functional properties were investigated by stress-strain measurement, thermogravimetric analysis (TGA), differential scanning calorimetry (DSC), X-ray photoelectron spectra (XPS), and so on. Our selection of polymeric materials for a SPE water electrolyzer used in a radiation environment was Pt + Ir applied Nafion N117 ion exchange membrane, VITON O-ring seal and polyimide insulator. (author)

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

Influence of impurities in Beryllium on tritium breeding ratio

International Nuclear Information System (INIS)

Yamauchi, M.; Ochiai, K.; Verzilov, Y.; Ito, M.; Wada, M.; Nishitani, T.

2004-01-01

Several neutronics experiments simulating fusion blankets have been conducted with 14 MeV neutron source to assess the reliability of nuclear analysis codes. However, the analyses have not always presented good agreements so far between calculated and measured tritium production rates. One of the reasons was considered as impurities in beryllium which has negligibly small neutron absorption cross section in low energy range. Chemical compositions of beryllium were analyzed by Inductively Coupled Plasma (ICP) method, and a pulsed neutron decay experiment discovered that the macroscopic neutron absorption cross section for beryllium medium may be about 30% larger than the value calculated by the data specified by manufacturing company. The influence of the impurities on the calculations was studied on the basis of the fusion DEMO-reactor blanket design. As a result of the study, it was made clear that the impurities affect the local tritium production rates when the size of beryllium medium is more than 20-30 mean free paths (30-40 cm) in thickness. In case of some blanket designs that meet the above condition, the effect on tritium breeding ratio may become as large as about 4%. (author)

Influence of impurities in Beryllium on tritium breeding ratio

Energy Technology Data Exchange (ETDEWEB)

Yamauchi, M; Ochiai, K; Verzilov, Y; Ito, M; Wada, M; Nishitani, T [Japan Atomic Energy Research Inst., Tokai, Ibaraki (Japan). Tokai Research Establishment

2004-03-01

Several neutronics experiments simulating fusion blankets have been conducted with 14 MeV neutron source to assess the reliability of nuclear analysis codes. However, the analyses have not always presented good agreements so far between calculated and measured tritium production rates. One of the reasons was considered as impurities in beryllium which has negligibly small neutron absorption cross section in low energy range. Chemical compositions of beryllium were analyzed by Inductively Coupled Plasma (ICP) method, and a pulsed neutron decay experiment discovered that the macroscopic neutron absorption cross section for beryllium medium may be about 30% larger than the value calculated by the data specified by manufacturing company. The influence of the impurities on the calculations was studied on the basis of the fusion DEMO-reactor blanket design. As a result of the study, it was made clear that the impurities affect the local tritium production rates when the size of beryllium medium is more than 20-30 mean free paths (30-40 cm) in thickness. In case of some blanket designs that meet the above condition, the effect on tritium breeding ratio may become as large as about 4%. (author)

Potential role of the Fast Flux Test Facility and the advanced test reactor in the U.S. tritium production system

Energy Technology Data Exchange (ETDEWEB)

Dautel, W.A.

1996-10-01

The Deparunent of Energy is currently engaged in a dual-track strategy to develop an accelerator and a conunercial light water reactor (CLWR) as potential sources of tritium supply. New analysis of the production capabilities of the Fast Flux Test Facility (FFTF) at the Hanford Site argues for considering its inclusion in the tritium supply,system. The use of the FFTF (alone or together with the Advanced Test Reactor [ATR] at the Idaho National Engineering Laboratory) as an integral part of,a tritium production system would help (1) ensure supply by 2005, (2) provide additional time to resolve institutional and technical issues associated with the- dual-track strategy, and (3) reduce discounted total life-cycle`costs and near-tenn annual expenditures for accelerator-based systems. The FFRF would also provide a way to get an early start.on dispositioning surplus weapons-usable plutonium as well as provide a source of medical isotopes. Challenges Associated With the Dual-Track Strategy The Departinent`s purchase of either a commercial reactor or reactor irradiation services faces challenging institutional issues associated with converting civilian reactors to defense uses. In addition, while the technical capabilities of the individual components of the accelerator have been proven, the entire system needs to be demonstrated and scaled upward to ensure that the components work toge ther 1548 as a complete production system. These challenges create uncertainty over the ability of the du2a-track strategy to provide an assured tritium supply source by 2005. Because the earliest the accelerator could come on line is 2007, it would have to operate at maximum capacity for the first few years to regenerate the reserves lost through radioactive decay aftei 2005.

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

Deuterium migration in nuclear graphite: Consequences for the behavior of tritium in CO{sub 2}-cooled reactors and for the decontamination of irradiated graphite waste

Energy Technology Data Exchange (ETDEWEB)

Le Guillou, M. [Institut de Physique Nucléaire de Lyon, CNRS/IN2P3 UMR 5822, Université Claude Bernard Lyon 1, Université de Lyon – 4, rue Enrico Fermi, F-69622 Villeurbanne cedex (France); Agence nationale pour la gestion des déchets radioactifs, DRD/CM – 1-7, rue Jean Monnet, Parc de la Croix-Blanche, F-92298 Châtenay-Malabry cedex (France); Toulhoat, N., E-mail: nelly.toulhoat@univ-lyon1.fr [Institut de Physique Nucléaire de Lyon, CNRS/IN2P3 UMR 5822, Université Claude Bernard Lyon 1, Université de Lyon – 4, rue Enrico Fermi, F-69622 Villeurbanne cedex (France); CEA/DEN – Centre de Saclay, F-91191 Gif-sur-Yvette cedex (France); Pipon, Y. [Institut de Physique Nucléaire de Lyon, CNRS/IN2P3 UMR 5822, Université Claude Bernard Lyon 1, Université de Lyon – 4, rue Enrico Fermi, F-69622 Villeurbanne cedex (France); Institut Universitaire Technologique, Université Claude Bernard Lyon 1, Université de Lyon – 43, boulevard du 11 novembre 1918, F-69622 Villeurbanne cedex (France); Moncoffre, N. [Institut de Physique Nucléaire de Lyon, CNRS/IN2P3 UMR 5822, Université Claude Bernard Lyon 1, Université de Lyon – 4, rue Enrico Fermi, F-69622 Villeurbanne cedex (France); Khodja, H. [Laboratoire d’Etude des Eléments Légers, CEA/DSM/IRAMIS/NIMBE, UMR 3299 SIS2M – Centre de Saclay, F-91191 Gif-sur-Yvette cedex (France)

2015-06-15

In this paper, we aim at understanding tritium behavior in the graphite moderator of French CO{sub 2}-cooled nuclear fission reactors (called UNGG for “Uranium Naturel-Graphite-Gaz”) to get information on its distribution and inventory in the irradiated graphite waste after their dismantling. These findings should be useful both to improve waste treatment processes and to foresee tritium behavior during reactor decommissioning and waste disposal operations. The purpose of the present work is to elucidate the effects of temperature on the behavior of tritium during reactor operation. Furthermore, it aims at exploring options of thermal decontamination. For both purposes, annealing experiments were carried out in inert atmosphere as well as in thermal conditions as close as possible to those encountered in UNGG reactors and in view of a potential decontamination in humid gas. D{sup +} ions were implanted into virgin nuclear graphite in order to simulate tritium displaced from its original structural site through recoil during reactor operation. The effect of thermal treatments on the mobility of the implanted deuterium was then investigated at temperatures ranging from 200 to 1200 °C, in inert atmosphere (vacuum or argon), in a gas simulating the UNGG coolant gas (mainly CO{sub 2}) or in humid nitrogen. Deuterium was analyzed by Nuclear Reaction Analysis (NRA) both at millimetric and micrometric scales. We have identified three main stages for the deuterium release. The first one corresponds to deuterium permeation through graphite open pores. The second and third ones are controlled by the progressive detrapping of deuterium located at different trapping sites and its successive migration through the crystallites and along crystallites and coke grains edges. Extrapolating the thermal behavior of deuterium to tritium, the results show that the release becomes significant above the maximum UNGG reactor temperature of 500 °C and should be lower than 30% of the

Calorimetric measurements of $^{163}$ holmium decay as tools to determine the electron neutrino mass

CERN Document Server

De Rújula, Alvaro

1982-01-01

Computes the spectrum of 'calorimetric' energy in the electron capture decay of /sup 163/Ho. A calorimetric experiment would yield an excellent determination of (/sup 163/Ho, /sup 163/Dy) mass difference. The proximity of the spectral endpoint to an atomic resonance makes the fraction of events that are sensitive to a non-zero neutrino mass superior in /sup 163/Ho decay than in tritium decay.

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

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)

Long-lived radicals produced by γ-irradiation or vital activity in plants, animals, cells, and protein solution: their observation and inhomogeneous decay dynamics

International Nuclear Information System (INIS)

Miyazaki, Tetsuo; Morikawa, Akiyuki; Kumagai, Jun; Ikehata, Masateru; Koana, Takao; Kikuchi, Shoshi

2002-01-01

Long-lived radicals produced by γ-irradiation or vital activity in plants, animals, cells, and protein (albumin) solution were studied by electron spin resonance spectroscopy. Long-lived radicals produced by vital activity exist in biological systems, such as plants, animals, and cells, in the range of 0.1-20 nmol g -1 . Since vital organs keep the radicals at a constant concentration, the radicals are probably related to life conservation. Long-lived radicals are also produced by γ-irradiation of cells or protein solution. The radicals decay after death of living things or after γ-irradiation. We found that the decay dynamics in all biological systems can be expressed by the same kinetic equation of an inhomogeneous reaction

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

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

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

Cosmogenic production of tritium in dark matter detectors

Science.gov (United States)

Amaré, J.; Castel, J.; Cebrián, S.; Coarasa, I.; Cuesta, C.; Dafni, T.; Galán, J.; García, E.; Garza, J. G.; Iguaz, F. J.; Irastorza, I. G.; Luzón, G.; Martínez, M.; Mirallas, H.; Oliván, M. A.; Ortigoza, Y.; Ortiz de Solórzano, A.; Puimedón, J.; Ruiz-Chóliz, E.; Sarsa, M. L.; Villar, J. A.; Villar, P.

2018-01-01

The direct detection of dark matter particles requires ultra-low background conditions at energies below a few tens of keV. Radioactive isotopes are produced via cosmogenic activation in detectors and other materials and those isotopes constitute a background source which has to be under control. In particular, tritium is specially relevant due to its decay properties (very low endpoint energy and long half-life) when induced in the detector medium, and because it can be generated in any material as a spallation product. Quantification of cosmogenic production of tritium is not straightforward, neither experimentally nor by calculations. In this work, a method for the calculation of production rates at sea level has been developed and applied to some of the materials typically used as targets in dark matter detectors (germanium, sodium iodide, argon and neon); it is based on a selected description of tritium production cross sections over the entire energy range of cosmic nucleons. Results have been compared to available data in the literature, either based on other calculations or from measurements. The obtained tritium production rates, ranging from a few tens to a few hundreds of nuclei per kg and per day at sea level, point to a significant contribution to the background in dark matter experiments, requiring the application of specific protocols for target material purification, material storing underground and limiting the time the detector is on surface during the building process in order to minimize the exposure to the most dangerous cosmic ray components.

Tritium levels in milk in the vicinity of chronic tritium releases

International Nuclear Information System (INIS)

Le Goff, P.; Guétat, Ph.; Vichot, L.; Leconte, N.; Badot, P.M.; Gaucheron, F.; Fromm, M.

2016-01-01

Tritium is the radioactive isotope of hydrogen. It can be integrated into most biological molecules. Even though its radiotoxicity is weak, the effects of tritium can be increased following concentration in critical compartments of living organisms. For a better understanding of tritium circulation in the environment and to highlight transfer constants between compartments, we studied the tritiation of different agricultural matrices chronically exposed to tritium. Milk is one of the most frequently monitored foodstuffs in the vicinity of points known for chronic release of radionuclides firstly because dairy products find their way into most homes but also because it integrates deposition over large areas at a local scale. It is a food which contains all the main nutrients, especially proteins, carbohydrates and lipids. We thus studied the tritium levels of milk in chronic exposure conditions by comparing the tritiation of the main hydrogenated components of milk, first, component by component, then, sample by sample. Significant correlations were found between the specific activities of drinking water and free water of milk as well as between the tritium levels of cattle feed dry matter and of the main organic components of milk. Our findings stress the importance of the metabolism on the distribution of tritium in the different compartments. Overall, dilution of hydrogen in the environmental compartments was found to play an important role dimming possible isotopic effects even in a food chain chronically exposed to tritium. - Highlights: • Tritium can be incorporated in all the hydrogenated components of milk. • Components' isotopic ratios T/H of chronically exposed milk remain in the same range. • In environmental conditions, distribution of tritium in milk components varies. • Metabolism plays a role in the distribution of tritium in the components of milk. • In environmental conditions, dilution of hydrogen dims possible isotopic effects.

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

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

JET experiments with tritium and deuterium–tritium mixtures

Energy Technology Data Exchange (ETDEWEB)

Horton, Lorne, E-mail: Lorne.Horton@jet.uk [JET Exploitation Unit, Culham Science Centre, Abingdon OX14 3DB (United Kingdom); European Commission, B-1049 Brussels (Belgium); EUROfusion Consortium, JET, Culham Science Centre, Abingdon OX14 3DB (United Kingdom); Batistoni, P. [Unità Tecnica Fusione - ENEA C. R. Frascati - via E. Fermi 45, Frascati (Roma), 00044, Frascati (Italy); EUROfusion Consortium, JET, Culham Science Centre, Abingdon OX14 3DB (United Kingdom); Boyer, H.; Challis, C.; Ćirić, D. [CCFE, Culham Science Centre, Abingdon OX14 3DB, Oxon (United Kingdom); EUROfusion Consortium, JET, Culham Science Centre, Abingdon OX14 3DB (United Kingdom); Donné, A.J.H. [EUROfusion Programme Management Unit, Culham Science Centre, Abingdon OX14 3DB (United Kingdom); FOM Institute DIFFER, PO Box 1207, NL-3430 BE Nieuwegein (Netherlands); EUROfusion Consortium, JET, Culham Science Centre, Abingdon OX14 3DB (United Kingdom); Eriksson, L.-G. [European Commission, B-1049 Brussels (Belgium); EUROfusion Consortium, JET, Culham Science Centre, Abingdon OX14 3DB (United Kingdom); Garcia, J. [CEA, IRFM, F-13108 Saint Paul Lez Durance (France); EUROfusion Consortium, JET, Culham Science Centre, Abingdon OX14 3DB (United Kingdom); Garzotti, L.; Gee, S. [CCFE, Culham Science Centre, Abingdon OX14 3DB, Oxon (United Kingdom); EUROfusion Consortium, JET, Culham Science Centre, Abingdon OX14 3DB (United Kingdom); Hobirk, J. [Max-Planck-Institut für Plasmaphysik, D-85748 Garching (Germany); EUROfusion Consortium, JET, Culham Science Centre, Abingdon OX14 3DB (United Kingdom); Joffrin, E. [CEA, IRFM, F-13108 Saint Paul Lez Durance (France); EUROfusion Consortium, JET, Culham Science Centre, Abingdon OX14 3DB (United Kingdom); and others

2016-11-01

Highlights: • JET is preparing for a series of experiments with tritium and deuterium–tritium mixtures. • Physics objectives include integrated demonstration of ITER operating scenarios, isotope and alpha physics. • Technology objectives include neutronics code validation, material studies and safety investigations. • Strong emphasis on gaining experience in operation of a nuclear tokamak and training scientists and engineers for ITER. - Abstract: Extensive preparations are now underway for an experiment in the Joint European Torus (JET) using tritium and deuterium–tritium mixtures. The goals of this experiment are described as well as the progress that has been made in developing plasma operational scenarios and physics reference pulses for use in deuterium–tritium and full tritium plasmas. At present, the high performance plasmas to be tested with tritium are based on either a conventional ELMy H-mode at high plasma current and magnetic field (operation at up to 4 MA and 4 T is being prepared) or the so-called improved H-mode or hybrid regime of operation in which high normalised plasma pressure at somewhat reduced plasma current results in enhanced energy confinement. Both of these regimes are being re-developed in conjunction with JET's ITER-like Wall (ILW) of beryllium and tungsten. The influence of the ILW on plasma operation and performance has been substantial. Considerable progress has been made on optimising performance with the all-metal wall. Indeed, operation at the (normalised) ITER reference confinement and pressure has been re-established in JET albeit not yet at high current. In parallel with the physics development, extensive technical preparations are being made to operate JET with tritium. The state and scope of these preparations is reviewed, including the work being done on the safety case for DT operation and on upgrading machine infrastructure and diagnostics. A specific example of the latter is the planned calibration at

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

Technical/ administrative options for managing tritium MCL exceedances in P-area groundwater and Steel Creek

Energy Technology Data Exchange (ETDEWEB)

Ross, J. [Savannah River Site (SRS), Aiken, SC (United States). Savannah River National Lab. (SRNL)

2017-04-01

This white paper was requested by the Core Team (United States Department of Energy [USDOE], United States Environmental Protection Agency [USEPA], and South Carolina Department of Health and Environmental Control [SCDHEC]) at the P-Area Groundwater (PAGW) Operable Unit (OU) Scoping Meeting held in January 2017 to discuss recent data and potential alternatives in support of a focused Corrective Measures Study/Feasibility Study (CMS/FS). This white paper presents an overview of the problem, and a range of technical and administrative options for addressing the tritium contamination in groundwater and Steel Creek. As tritium cannot be treated practicably, alternatives are limited to media transfer, containment and natural attenuation principally relying on radioactive decay. Using other groundwater OU decisions involving tritium as precedent, Savannah River Nuclear Solutions (SRNS) recommends that final tritium alternatives be evaluated in a CMS/FS, understanding that the likely preferred remedy will include natural attenuation with land use controls (LUCs). This is based on the inability to significantly reduce tritium impact to Steel Creek using an engineered solution as compared to natural attenuation. The timing of this evaluation could be conducted concurrently with the final remedy evaluation for volatile organic compounds (VOCs).

Investigating Unsaturated Zone Travel Times with Tritium and Stable Isotopes

Science.gov (United States)

Visser, A.; Thaw, M.; Van der Velde, Y.

2017-12-01

Travel times in the unsaturated zone are notoriously difficult to assess. Travel time tracers relying on the conservative transport of dissolved (noble) gases (tritium-helium, CFCs or SF6) are not applicable. Large water volume requirements of other cosmogenic radioactive isotopes (sulfur-35, sodium-22) preclude application in the unsaturated zone. Prior investigations have relied on models, introduced tracers, profiles of stable isotopes or tritium, or a combination of these techniques. Significant unsaturated zone travel times (UZTT) complicate the interpretation of stream water travel time tracers by ranked StorAge Selection (rSAS) functions. Close examination of rSAS functions in a sloping soil lysimeter[1] show the effect of the UZTT on the shape of the rSAS cumulative distribution function. We studied the UZTT at the Southern Sierra Critical Zone Observatory (SS-CZO) using profiles of tritium and stable isotopes (18O and 2H) in the unsaturated zone, supported by soil water content data. Tritium analyses require 100-500 mL of soil water and therefore large soil samples (1-5L), and elaborate laboratory procedures (oven drying, degassing and noble gas mass spectrometry). The high seasonal and interannual variability in precipitation of the Mediterranean climate, variable snow pack and high annual ET/P ratios lead to a dynamic hydrology in the deep unsaturated soils and regolith and highly variable travel time distributions. Variability of the tritium concentration in precipitation further complicates direct age estimates. Observed tritium profiles (>3 m deep) are interpreted in terms of advective and dispersive vertical transport of the input variability and radioactive decay of tritium. Significant unsaturated zone travel times corroborate previously observed low activities of short-lived cosmogenic radioactive nuclides in stream water. Under these conditions, incorporating the UZTT is critical to adequately reconstruct stream water travel time distributions. 1

Results of neutron irradiation of liquid lithium saturated with deuterium

International Nuclear Information System (INIS)

Tazhibayeva, Irina; Ponkratov, Yuriy; Kulsartov, Timur; Gordienko, Yuriy; Skakov, Mazhyn; Zaurbekova, Zhanna; Lyublinski, Igor; Vertkov, Alexey; Mazzitelli, Giuseppe

2017-01-01

Highlights: • The results on neutron irradiation of liquid lithium saturated with deuterium at the IVG.1M research reactor are described. • At temperatures below 573 K the efficiency coefficient of tritium release is well described by the expression K = 0.015 exp(−14/RT), and above 623 K − K = 10 9 exp(−144/RT). • The T 2 molecules contribution into the overall tritium release becomes apparent at temperatures higher than 673 K and increases with the temperature rise. - Abstract: This paper describes the results on neutron irradiation of liquid lithium saturated with deuterium at the IVG.1 M research reactor. The neutron flux at the reactor core center at 2 MW was 5 10 −13 cm −2 s −1 . The efficiency coefficients of helium and tritium release from lithium saturated with deuterium were calculated. The tritium interaction with lithium atoms (formation and dissociation of lithium tritide) has an effect on tritium release. An increment of sample’s temperature results in tritium release acceleration due to rising of the dissociation rate of lithium tritide. At temperatures below 573 K the efficiency coefficient of tritium release is well described by the expression K = 0.015 exp(−14/RT), and above 623 K − K = 10 9 exp(-144/RT). The T 2 molecules contribution into the overall tritium release becomes apparent at temperatures higher than 673 K and increases with the temperature rise.

Overview of tritium processing development at the tritium systems test assembly

International Nuclear Information System (INIS)

Anderson, J.L.

1986-01-01

The Tritium Systems Test Assembly (TSTA) at the Los Alamos National Laboratory has been operating with tritium since June 1984. Presently there are some 50 g of tritium in the main processing loop. This 50 g has been sufficient to do a number of experiments involving the cryogenic distillation isotope separation system and to integrate the fuel cleanup system into the main fuel processing loop. In January 1986 two major experiments were conducted. During these experiments the fuel cleanup system was integrated, through the transfer pumping system, with the isotope separation system, thus permitting testing on the integrated fuel processing loop. This integration of these systems leaves only the main vacuum system to be integrated into the TSTA fuel processing loop. In September 1986 another major tritium experiment was performed in which the integrated loop was operated, the tritium inventory increased to 50 g and additional measurements on the performance of the distillation system were taken. In the period June 1984 through September 1986 the TSTA system has processed well over 10 8 Ci of tritium. Total tritium emissions to the environment over this period have been less than 15 Ci. Personnel exposures during this period have totaled less than 100 person-mRem. To date, the development of tritium technology at TSTA has proceeded in progressive and orderly steps. In two years of operation with tritium, no major design flows have been uncovered

Deuterium Depth Profile in Neutron-Irradiated Tungsten Exposed to Plasma

International Nuclear Information System (INIS)

Shimada, Masashi; Cao, G.; Hatano, Y.; Oda, T.; Oya, Y.; Hara, M.; Calderoni, P.

2011-01-01

The effect of radiation damage has been mainly simulated using high-energy ion bombardment. The ions, however, are limited in range to only a few microns into the surface. Hence, some uncertainty remains about the increase of trapping at radiation damage produced by 14 MeV fusion neutrons, which penetrate much farther into the bulk material. With the Japan-US joint research project: Tritium, Irradiations, and Thermofluids for America and Nippon (TITAN), the tungsten samples (99.99 % pure from A.L.M.T., 6mm in diameter, 0.2mm in thickness) were irradiated to high flux neutrons at 50 C and to 0.025 dpa in the High Flux Isotope Reactor (HFIR) at the Oak Ridge National Laboratory (ORNL). Subsequently, the neutron-irradiated tungsten samples were exposed to a high-flux deuterium plasma (ion flux: 1021-1022 m-2s-1, ion fluence: 1025-1026 m-2) in the Tritium Plasma Experiment (TPE) at the Idaho National Laboratory (INL). First results of deuterium retention in neutron-irradiated tungsten exposed in TPE have been reported previously. This paper presents the latest results in our on-going work of deuterium depth profiling in neutron-irradiated tungsten via nuclear reaction analysis. The experimental data is compared with the result from non neutron-irradiated tungsten, and is analyzed with the Tritium Migration Analysis Program (TMAP) to elucidate the hydrogen isotope behavior such as retention and depth distribution in neutron-irradiated and non neutron-irradiated tungsten.

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

Tritium labeling of amino acids and peptides with liquid and solid tritium

International Nuclear Information System (INIS)

Peng, C.T.; Hua, R.L.; Souers, P.C.; Coronado, P.R.

1988-01-01

Amino acids and peptides were labeled with liquid and solid tritium at 21 K and 9 K. At these low temperatures radiation degradation is minimal, and tritium incorporation increases with tritium concentration and exposure time. Ring saturation in L-phenyl-alanine does not occur. Peptide linkage in oligopeptides is stable toward tritium. Deiodination in 3-iodotyrosine and 3,5-diiodotyrosine occurs readily and proceeds in steps by losing one iodine atom at a time. Nickel and noble metal supported catalysts when used as supports for dispersion of the substrate promote tritium labeling at 21 K. Our study shows that both liquid and solid tritium are potentially useful agents for labeling peptides and proteins. 11 refs., 1 fig., 3 tabs

Tritium labeling of amino acids and peptides with liquid and solid tritium

International Nuclear Information System (INIS)

Souers, P.C.; Coronado, P.R.; Peng, C.T.; Hua, R.L.

1988-01-01

Amino acids and peptides were labeled with liquid and solid tritium at 21/degree/K and 9/degree/K. At these low temperatures radiation degradation is minimal, and tritium incorporation increases with tritium concentration and exposure time. Ring saturation in L-phenylalanine does not occur. Peptide linkage in oligopeptides is stable toward tritium. Deiodination in 3-iodotyrosine and 3,5-diiodotyrosine occurs readily and proceeds in steps by losing one iodine atom at a time. Nickel and noble metal supported catalysts when used as supports for dispersion of the substrate promote tritium labeling at 21 K. Our study shows that both liquid and solid tritiums are potentially useful agents for labeling peptides and proteins

Tritium contaminated waste management at the tritium systems test assembly

International Nuclear Information System (INIS)

Jalbert, R.A.; Carlson, R.V.

1987-01-01

The Tritium Systems Test Assembly (TSTA) at Los Alamos continues to move toward full operation of an integrated, full-sized, computer-controlled fusion fuel processing loop. Concurrent nonloop experiments further the development of advanced tritium technologies and handling methods. Since tritium operations began in June 1984, tritium contaminated wastes have been produced at TSTA that are roughly typical in kind and amount of those to be produced by tritium fueling operations at fusion reactors. Methods of managing these wastes are described, including information on some methods of decontamination so that equipment can be reused. Data are given on the kinds and amounts of wastes and the general level of contamination. Also included are data on environmental emissions and doses to personnel that have resulted from TSTA operations. Particular problems in waste managements are discussed

Current status of tritium calorimetry at TLK

Energy Technology Data Exchange (ETDEWEB)

Buekki-Deme, A.; Alecu, C.G.; Kloppe, B.; Bornschein, B. [Institute of Technical Physics, Tritium Laboratory Karsruhe - TLK, Karlsruhe Institute of Technology - KIT, Karlsruhe (Germany)

2015-03-15

Inside a tritium facility, calorimetry is an important analytical method as it is the only reference method for accountancy (it is based on the measurement of the heat generated by the radioactive decay). Presently, at Tritium Laboratory Karlsruhe (TLK), 4 calorimeters are in operation, one of isothermal type and three of inertial guidance control type (IGC). The volume of the calorimeters varies between 0.5 and 20.6 liters. About two years ago we started an extensive work to improve our calorimeters with regard to reliability and precision. We were forced to upgrade 3 of our 4 calorimeters due to the outdated interfaces and software. This work involved creating new LabView programs driving the devices, re-tuning control loops and replacing obsolete hardware components. In this paper we give a review on the current performance of our calorimeters, comparing it to recently available devices from the market and in the literature. We also show some ideas for a next generation calorimeter based on experiences with our IGC calorimeters and other devices reported in the literature. (authors)

Current status of tritium calorimetry at TLK

International Nuclear Information System (INIS)

Buekki-Deme, A.; Alecu, C.G.; Kloppe, B.; Bornschein, B.

2015-01-01

Inside a tritium facility, calorimetry is an important analytical method as it is the only reference method for accountancy (it is based on the measurement of the heat generated by the radioactive decay). Presently, at Tritium Laboratory Karlsruhe (TLK), 4 calorimeters are in operation, one of isothermal type and three of inertial guidance control type (IGC). The volume of the calorimeters varies between 0.5 and 20.6 liters. About two years ago we started an extensive work to improve our calorimeters with regard to reliability and precision. We were forced to upgrade 3 of our 4 calorimeters due to the outdated interfaces and software. This work involved creating new LabView programs driving the devices, re-tuning control loops and replacing obsolete hardware components. In this paper we give a review on the current performance of our calorimeters, comparing it to recently available devices from the market and in the literature. We also show some ideas for a next generation calorimeter based on experiences with our IGC calorimeters and other devices reported in the literature. (authors)

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)

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

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

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

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)

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)

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)

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

Study of measurement method of tritium induced in concrete of high-energy proton accelerator facilities

International Nuclear Information System (INIS)

Ohtsuka, N.; Ishihama, S.; Kunifuda, T.; Hayasaka, N.; Miura, T.

2001-01-01

Various long-loved radionuclides, 3 H, 7 Be, 22 Na, 51 Cr, 54 Mn, 56 Co, 57 Co, 60 Co, 134 Cs, 152 Eu and 154 Eu, have been produced in the shielding concrete of high energy proton accelerator facility through both nuclear spallation reactions and thermal neutron capture reactions of concrete elements, during machine operation. Tritium is the most important nuclide from the radiation protection. There were, however, few measurements of tritium concentration induced in the shielding concrete. In this study, the conditions of measurement method of tritium concentration induced in shielding concrete have been investigated using the activated shielding concrete of the 12 GeV proton beam-line tunnel at KEK and the standard rock (JG-1) irradiated of thermal neutron at the reactor. And the depth profiles of tritium induced in the shielding concrete of slow extracted proton beam line at KEK were determined using this method. (author)

Drinking water standard for tritium-what's the risk?

Science.gov (United States)

Kocher, D C; Hoffman, F O

2011-09-01

This paper presents an assessment of lifetime risks of cancer incidence associated with the drinking water standard for tritium established by the U.S. Environmental Protection Agency (USEPA); this standard is an annual-average maximum contaminant level (MCL) of 740 Bq L(-1). This risk assessment has several defining characteristics: (1) an accounting of uncertainty in all parameters that relate a given concentration of tritium in drinking water to lifetime risk (except the number of days of consumption of drinking water in a year and the number of years of consumption) and an accounting of correlations of uncertain parameters to obtain probability distributions that represent uncertainty in estimated lifetime risks of cancer incidence; (2) inclusion of a radiation effectiveness factor (REF) to represent an increased biological effectiveness of low-energy electrons emitted in decay of tritium compared with high-energy photons; (3) use of recent estimates of risks of cancer incidence from exposure to high-energy photons, including the dependence of risks on an individual's gender and age, in the BEIR VII report; and (4) inclusion of risks of incidence of skin cancer, principally basal cell carcinoma. By assuming ingestion of tritium in drinking water at the MCL over an average life expectancy of 80 y in females and 75 y in males, 95% credibility intervals of lifetime risks of cancer incidence obtained in this assessment are (0.35, 12) × 10(-4) in females and (0.30, 15) × 10(-4) in males. Mean risks, which are considered to provide the best single measure of expected risks, are about 3 × 10(-4) in both genders. In comparison, USEPA's point estimate of the lifetime risk of cancer incidence, assuming a daily consumption of drinking water of 2 L over an average life expectancy of 75.2 y and excluding an REF for tritium and incidence of skin cancer, is 5.6 × 10(-5). Probability distributions of annual equivalent doses to the whole body associated with the drinking

Quantification of the activity of tritium produced during the routine synthesis of (18)F fluorodeoxyglucose for positron emission tomography.

Science.gov (United States)

Marshall, C; Talboys, M A; Bukhari, S; Evans, W D

2014-06-01

Gamma emitting radioactive by-products generated during the cyclotron irradiation of (18)O labelled water by protons to produce (18)FDG (fluorodeoxyglucose) for positron emission tomography are well characterised. However, the production of tritium ((3)H) through the (18)O(p,t)(16)O nuclear reaction has not been investigated in detail. The aim of this study was to measure tritium activity produced during a large number of (18)FDG production runs in order to obtain a better perspective on its impact on radioactive waste management, particularly as regards storage and disposal. Tritium was assayed by liquid scintillation counting in recovered (18)O water from 24 separate production runs. The mean (SD) values of activity and activity concentration were 170 (20) kBq and 81 (8) kBq ml(-1) respectively. Both quantities were positively correlated with the activity of (18)F. Tritium was detected in much lower concentration in water used to rinse the target vessel. The activity of tritium is such that it is exempt from regulatory control and may be combined with bulk non-active waste for disposal as Very Low Level Waste. However, variations in the irradiation conditions or the procedures for the collection of recovered water might result in its classification as Low Level Waste, necessitating a more complex disposal regime.

Results of neutron irradiation of liquid lithium saturated with deuterium

Energy Technology Data Exchange (ETDEWEB)

Tazhibayeva, Irina, E-mail: tazhibayeva@ntsc.kz [Institute of Atomic Energy, National Nuclear Center of RK, Kurchatov (Kazakhstan); Ponkratov, Yuriy; Kulsartov, Timur; Gordienko, Yuriy; Skakov, Mazhyn; Zaurbekova, Zhanna [Institute of Atomic Energy, National Nuclear Center of RK, Kurchatov (Kazakhstan); Lyublinski, Igor [JSC «Red Star», Moscow (Russian Federation); NRNU «MEPhI», Moscow (Russian Federation); Vertkov, Alexey [JSC «Red Star», Moscow (Russian Federation); Mazzitelli, Giuseppe [ENEA, RC Frascati, Frascati (Italy)

2017-04-15

Highlights: • The results on neutron irradiation of liquid lithium saturated with deuterium at the IVG.1M research reactor are described. • At temperatures below 573 K the efficiency coefficient of tritium release is well described by the expression K = 0.015 exp(−14/RT), and above 623 K − K = 10{sup 9} exp(−144/RT). • The T{sub 2} molecules contribution into the overall tritium release becomes apparent at temperatures higher than 673 K and increases with the temperature rise. - Abstract: This paper describes the results on neutron irradiation of liquid lithium saturated with deuterium at the IVG.1 M research reactor. The neutron flux at the reactor core center at 2 MW was 5 10{sup −13} cm{sup −2} s{sup −1}. The efficiency coefficients of helium and tritium release from lithium saturated with deuterium were calculated. The tritium interaction with lithium atoms (formation and dissociation of lithium tritide) has an effect on tritium release. An increment of sample’s temperature results in tritium release acceleration due to rising of the dissociation rate of lithium tritide. At temperatures below 573 K the efficiency coefficient of tritium release is well described by the expression K = 0.015 exp(−14/RT), and above 623 K − K = 10{sup 9} exp(-144/RT). The T{sub 2} molecules contribution into the overall tritium release becomes apparent at temperatures higher than 673 K and increases with the temperature rise.

Effect of excess ozone on UV-stimulated tritium oxidation

International Nuclear Information System (INIS)

Hasegawa, Kiyoshi; Horii, Kazuhiro; Matsuyama, Masao; Watanabe, Kuniaki.

1995-01-01

The authors have reported that the oxidation of tritium is considerably accelerated by irradiating a mixture gas of HT(H 2 )-O 2 with UV-photons, and this UV-stimulated HT oxidation is mainly due to the formation of intermediates such as ozone and activated oxygen species. This suggests that the oxidation will be much more enhanced in the presence of excess ozone in the reaction system. To examine this possibility, effects of the excess ozone on the UV-stimulated HT oxidation was experimentally studied on the one hand, and reaction mechanisms were investigated by developing a computer simulation program applicable to the three-component system of HT(H 2 )-O 2 -O 3 . The formation rate of HTO was measured for gas mixtures consisting of O 2 (75.5 Torr), O 3 (0.5-2% of O 2 ), H 2 (0.1-3% of O 2 ) and HT(H 2 /HT=12000). The experiments showed considerable enhancement of the HTO production rate in the presence of excess ozone by UV-photons from a low pressure mercury lamp(5W). The time course of the reaction was reproduced quite well by computer simulation, indicating that the assumed reaction mechanism is valid. This is also supported by observations that computer simulation reproduced the experimentally observed dependence of ozone decomposition rate on ozone and hydrogen pressures under the UV-irradiation. Those results showed that UV-stimulated HT oxidation was accelerated by about 14000 times in the presence of excess ozone. It strongly suggests that the UV-stimulated oxidation in the presence of excess ozone will be applicable to tritium handling systems as a non-catalytic tritium removal method. (author)

Experiment designed to measure the RBE of tritium for the induction of myeloid leukaemia in animals

Energy Technology Data Exchange (ETDEWEB)

Johnson, J R; Myers, D K; Gragtmans, N J

1986-01-01

The range in RBE vales measured for tritium can be attributed to differences in the biological endpoints measured, the reference radiation to which the effects of tritium were compared, and the tritium dosimetry of the particular study. Since the principal risk of low-level irradiation is the induction of cancers, it would be desirable to utilise this endpoint in tritium RBE experiments if these experiments are to be used to evaluate the quality factor for tritium. Furthermore, it would be desirable to use 200 k Vp X rays as the reference radiation since this radiation was suggested by ICRP as the standard reference to be used in the calculation of dose equivalents. Acute myeloid leukaemia is one of the earliest recognised examples of radiogenic cancer in humans and this endpoint has also been the subject of animal studies. A brief review is given of these animal studies to see if this endpoint is suitable for an experiment to measure the tritium RBE relative to 200 k Vp X rays. It was concluded that the male CBA/H mouse would be a suitable species and an experiment involving 5000 animals in four to five year study would be required to provide a useful estimate of the RBE for tritium.

Analysis of a global database containing tritium in precipitation

Energy Technology Data Exchange (ETDEWEB)

Buckley, R. L. [Savannah River Site (SRS), Aiken, SC (United States); Rabun, R. L. [Savannah River Site (SRS), Aiken, SC (United States); Heath, M. [Savannah River Site (SRS), Aiken, SC (United States)

2016-02-17

The International Atomic Energy Agency (IAEA) directed the collection of tritium in water samples from the mid-1950s to 2009. The Global Network of Isotopes in Precipitation (GNIP) data examined the airborne movement of isotope releases to the environment, with an objective of collecting spatial data on the isotope content of precipitation across the globe. The initial motivation was to monitor atmospheric thermonuclear test fallout through tritium, deuterium, and oxygen isotope concentrations, but after the 1970s the focus changed to being an observation network of stable hydrogen and oxygen isotope data for hydrologic studies. The GNIP database provides a wealth of tritium data collections over a long period of time. The work performed here primarily examined data features in the past 30 years (after much of the effects of above-ground nuclear testing in the late 1950s to early 1960s decayed away), revealing potentially unknown tritium sources. The available data at GNIP were reorganized to allow for evaluation of trends in the data both temporally and spatially. Several interesting cases were revealed, including relatively high measured concentrations in the Atlantic and Indian Oceans, Russia, Norway, as well as an increase in background concentration at a collector in South Korea after 2004. Recent data from stations in the southeastern United States nearest to the Savannah River Site do not indicate any high values. Meteorological impacts have not been considered in this study. Further research to assess the likely source location of interesting cases using transport simulations and/or literature searches is warranted.

Tritium levels in milk in the vicinity of chronic tritium releases.

Science.gov (United States)

Le Goff, P; Guétat, Ph; Vichot, L; Leconte, N; Badot, P M; Gaucheron, F; Fromm, M

2016-01-01

Tritium is the radioactive isotope of hydrogen. It can be integrated into most biological molecules. Even though its radiotoxicity is weak, the effects of tritium can be increased following concentration in critical compartments of living organisms. For a better understanding of tritium circulation in the environment and to highlight transfer constants between compartments, we studied the tritiation of different agricultural matrices chronically exposed to tritium. Milk is one of the most frequently monitored foodstuffs in the vicinity of points known for chronic release of radionuclides firstly because dairy products find their way into most homes but also because it integrates deposition over large areas at a local scale. It is a food which contains all the main nutrients, especially proteins, carbohydrates and lipids. We thus studied the tritium levels of milk in chronic exposure conditions by comparing the tritiation of the main hydrogenated components of milk, first, component by component, then, sample by sample. Significant correlations were found between the specific activities of drinking water and free water of milk as well as between the tritium levels of cattle feed dry matter and of the main organic components of milk. Our findings stress the importance of the metabolism on the distribution of tritium in the different compartments. Overall, dilution of hydrogen in the environmental compartments was found to play an important role dimming possible isotopic effects even in a food chain chronically exposed to tritium. Copyright © 2015 Elsevier Ltd. All rights reserved.

Movement of a tritium plume in shallow groundwater at a legacy low-level radioactive waste disposal site in eastern Australia.

Science.gov (United States)

Hughes, C E; Cendón, D I; Harrison, J J; Hankin, S I; Johansen, M P; Payne, T E; Vine, M; Collins, R N; Hoffmann, E L; Loosz, T

2011-10-01

Between 1960 and 1968 low-level radioactive waste was buried in a series of shallow trenches near the Lucas Heights facility, south of Sydney, Australia. Groundwater monitoring carried out since the mid 1970s indicates that with the exception of tritium, no radioactivity above typical background levels has been detected outside the immediate vicinity of the trenches. The maximum tritium level detected in ground water was 390 kBq/L and the median value was 5400 Bq/L, decay corrected to the time of disposal. Since 1968, a plume of tritiated water has migrated from the disposal trenches and extends at least 100 m from the source area. Tritium in rainfall is negligible, however leachate from an adjacent and fill represents a significant additional tritium source. Study data indicate variation in concentration levels and plume distribution in response to wet and dry climatic periods and have been used to determine pathways for tritium migration through the subsurface.

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

JET experiments with tritium and deuterium–tritium mixtures

NARCIS (Netherlands)

Horton, L.; Batistoni, P.; Boyer, H.; Challis, C.; Ciric, D.; Donne, A. J. H.; Eriksson, L. G.; Garcia, J.; Garzotti, L.; Gee, S.; Hobirk, J.; Joffrin, E.; Jones, T.; King, D. B.; Knipe, S.; Litaudon, X.; Matthews, G. F.; Monakhov, I.; Murari, A.; Nunes, I.; Riccardo, V.; Sips, A. C. C.; Warren, R.; Weisen, H.; Zastrow, K. D.

2016-01-01

Extensive preparations are now underway for an experiment in the Joint European Torus (JET) using tritium and deuterium–tritium mixtures. The goals of this experiment are described as well as the progress that has been made in developing plasma operational scenarios and physics reference pulses for

Warm Dark Matter Sterile Neutrinos in Electron Capture and Beta Decay Spectra

Directory of Open Access Journals (Sweden)

O. Moreno

2016-01-01

Full Text Available We briefly review the motivation to search for sterile neutrinos in the keV mass scale, as dark matter candidates, and the prospects to find them in beta decay or electron capture spectra, with a global perspective. We describe the fundamentals of the neutrino flavor-mass eigenstate mismatch that opens the possibility of detecting sterile neutrinos in such ordinary nuclear processes. Results are shown and discussed for the effect of heavy neutrino emission in electron capture in Holmium 163 and in two isotopes of Lead, 202 and 205, as well as in the beta decay of Tritium. We study the deexcitation spectrum in the considered cases of electron capture and the charged lepton spectrum in the case of Tritium beta decay. For each of these cases, we define ratios of integrated transition rates over different regions of the spectrum under study and give new results that may guide and facilitate the analysis of possible future measurements, paying particular attention to forbidden transitions in Lead isotopes.

Role of soil-to-leaf tritium transfer in controlling leaf tritium dynamics: Comparison of experimental garden and tritium-transfer model results.

Science.gov (United States)

Ota, Masakazu; Kwamena, Nana-Owusua A; Mihok, Steve; Korolevych, Volodymyr

2017-11-01

Environmental transfer models assume that organically-bound tritium (OBT) is formed directly from tissue-free water tritium (TFWT) in environmental compartments. Nevertheless, studies in the literature have shown that measured OBT/HTO ratios in environmental samples are variable and generally higher than expected. The importance of soil-to-leaf HTO transfer pathway in controlling the leaf tritium dynamics is not well understood. A model inter-comparison of two tritium transfer models (CTEM-CLASS-TT and SOLVEG-II) was carried out with measured environmental samples from an experimental garden plot set up next to a tritium-processing facility. The garden plot received one of three different irrigation treatments - no external irrigation, irrigation with low tritium water and irrigation with high tritium water. The contrast between the results obtained with the different irrigation treatments provided insights into the impact of soil-to-leaf HTO transfer on the leaf tritium dynamics. Concentrations of TFWT and OBT in the garden plots that were not irrigated or irrigated with low tritium water were variable, responding to the arrival of the HTO-plume from the tritium-processing facility. In contrast, for the plants irrigated with high tritium water, the TFWT concentration remained elevated during the entire experimental period due to a continuous source of high HTO in the soil. Calculated concentrations of OBT in the leaves showed an initial increase followed by quasi-equilibration with the TFWT concentration. In this quasi-equilibrium state, concentrations of OBT remained elevated and unchanged despite the arrivals of the plume. These results from the model inter-comparison demonstrate that soil-to-leaf HTO transfer significantly affects tritium dynamics in leaves and thereby OBT/HTO ratio in the leaf regardless of the atmospheric HTO concentration, only if there is elevated HTO concentrations in the soil. The results of this work indicate that assessment models

Tritium plume dynamics in the shallow unsaturated zone in an arid environment

Science.gov (United States)

Maples, S.R.; Andraski, Brian J.; Stonestrom, David A.; Cooper, C.A.; Pohll, G.; Michel, R.L.

2014-01-01

The spatiotemporal variability of a tritium plume in the shallow unsaturated zone and the mechanisms controlling its transport were evaluated during a 10-yr study. Plume movement was minimal and its mass declined by 68%. Upward-directed diffusive-vapor tritium fluxes and radioactive decay accounted for most of the observed plume-mass declines.Effective isolation of tritium (3H) and other contaminants at waste-burial facilities requires improved understanding of transport processes and pathways. Previous studies documented an anomalously widespread (i.e., theoretically unexpected) distribution of 3H (>400 m from burial trenches) in a dry, sub-root-zone gravelly layer (1–2-m depth) adjacent to a low-level radioactive waste (LLRW) burial facility in the Amargosa Desert, Nevada, that closed in 1992. The objectives of this study were to: (i) characterize long-term, spatiotemporal variability of 3H plumes; and (ii) quantify the processes controlling 3H behavior in the sub-root-zone gravelly layer beneath native vegetation adjacent to the facility. Geostatistical methods, spatial moment analyses, and mass flux calculations were applied to a spatiotemporally comprehensive, 10-yr data set (2001–2011). Results showed minimal bulk-plume advancement during the study period and limited Fickian spreading of mass. Observed spreading rates were generally consistent with theoretical vapor-phase dispersion. The plume mass diminished more rapidly than would be expected from radioactive decay alone, indicating net efflux from the plume. Estimates of upward 3H efflux via diffusive-vapor movement were >10× greater than by dispersive-vapor or total-liquid movement. Total vertical fluxes were >20× greater than lateral diffusive-vapor fluxes, highlighting the importance of upward migration toward the land surface. Mass-balance calculations showed that radioactive decay and upward diffusive-vapor fluxes contributed the majority of plume loss. Results indicate that plume losses

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

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)

Behavioral effects of chronic exposure to organically bound tritium and tritiated water

International Nuclear Information System (INIS)

Radwan, I.

1982-01-01

The results of developmental testing of F-1 and F-2-animals indicate that in HTO group no differences with control animals were observed, while there was delay in development of righting reflex in F-1-animals of T-food exposed rats, but the difference was not statistically significant. The comparison of data obtained for F-1 and F2-generation shows no cumulative effect of tritium irradiation in subsequent generations. The effects of HTO and organically bound tritium exposure on acute individual locomotor activity of 70 days old rats showed statistically significant hypoactivity of females of t-food group. The differences with the control animals were highest and statistically significant in first 20 minutes of their run in the maze, what suggests that tritium esposure alters the females reactivity to a novel situation. This effects may nor persists for the lifetime. The data of locomotor activity of 110 days old rats recorded in diurnal and nocturnal periods, showed no differences between HTO-group and control group and only slight but no statistically significant hypoactivity of females exposed to organically bound tritium. (orig./MG)

DESCRIPTION OF THE TRITIUM-PRODUCING BURNABLE ABSORBER ROD FOR THE COMMERCIAL LIGHT WATER REACTOR TTQP-1-015 Rev 19

Energy Technology Data Exchange (ETDEWEB)

Burns, Kimberly A.; Love, Edward F.; Thornhill, Cheryl K.

2012-02-01

Tritium-producing burnable absorber rods (TPBARs) used in the U.S. Department of Energy’s Tritium Readiness Program are designed to produce tritium when placed in a Westinghouse or Framatome 17x17 fuel assembly and irradiated in a pressurized water reactor (PWR). This document provides an unclassified description of the current design baseline for the TPBARs. This design baseline is currently valid only for Watts Bar reactor production cores. A description of the Lead Use TPBARs will not be covered in the text of the document, but the applicable drawings, specifications and test plan will be included in the appropriate appendices.

Tritium-assisted fusion breeders

International Nuclear Information System (INIS)

Greenspan, E.; Miley, G.H.

1983-08-01

This report undertakes a preliminary assessment of the prospects of tritium-assisted D-D fuel cycle fusion breeders. Two well documented fusion power reactor designs - the STARFIRE (D-T fuel cycle) and the WILDCAT (Cat-D fuel cycle) tokamaks - are converted into fusion breeders by replacing the fusion electric blankets with 233 U producing fission suppressed blankets; changing the Cat-D fuel cycle mode of operation by one of the several tritium-assisted D-D-based modes of operation considered; adjusting the reactor power level; and modifying the resulting plant cost to account for the design changes. Three sources of tritium are considered for assisting the D-D fuel cycle: tritium produced in the blankets from lithium or from 3 He and tritium produced in the client fission reactors. The D-D-based fusion breeders using tritium assistance are found to be the most promising economically, especially the Tritium Catalyzed Deuterium mode of operation in which the 3 He exhausted from the plasma is converted, by neutron capture in the blanket, into tritium which is in turn fed back to the plasma. The number of fission reactors of equal thermal power supported by Tritium Catalyzed Deuterium fusion breeders is about 50% higher than that of D-T fusion breeders, and the profitability is found to be slightly lower than that of the D-T fusion breeders

Changes of medullary hemopoiesis produced by chronic exposure to tritium oxide and external γ-radiation

International Nuclear Information System (INIS)

Murzina, L.D.; Muksinova, K.N.

1982-01-01

A comparative study of a chronic effect of tritium oxide ( 3 HOH) and external γ-radiation by 137 Cs on medullary hemopoiesis was conducted in experiments on Wistar rats. 3 HOH was administered for 3mos., 37x10 4 Bk per lg per of body mass daily (the absorbed dose 10.8 Gy), external irradiation was given in correlated values of dose rates and integral doses. Bone marrow depopulation was 1.9 times as deeper in rats exposed to 3 HOH as compared to that in irradiated rats. This difference is caused by early and stable inhibition of erythropoiesis with the administration of the radionuclide. The integral index showing the injuring effect of tritium on erythropoiesis was 4 times as high as compared to that of external γ-irradiation by 137 Cs. The time course of value of the proliferative pool of bone marrow granulocytes with the exposure to 2 types of radiation was monotypic. Differences in maturing and functioning granulocytic pools were marked in early time of the experiment

Thermal release of {sup 3}He from tritium aged LaNi{sub 4.25}Al{sub 0.75} hydride

Energy Technology Data Exchange (ETDEWEB)

Staack, G.C.; Crowder, M.L.; Klein, J.E. [Savannah River National Laboratory, Aiken, SC (United States)

2015-03-15

The Savannah River Site Tritium Facilities (SRS-TF) utilizes LANA.75 (LaNi{sub 4.25}Al{sub 0.75})in the tritium process to store hydrogen isotopes. The vast majority of {sup 3}He born from the radioactive decay of tritium stored in LANA.75 is trapped in the hydride metal matrix. The SRS-TF has multiple LANA.75 tritium storage beds that have been retired from service with significant quantities of He-3 trapped in the metal. To support He-3 recovery, the Savannah River National Laboratory (SRNL) conducted thermogravimetric analysis coupled with mass spectrometry (TGA-MS) on a tritium aged LANA.75 sample. TGA-MS testing was performed in an argon environment. Prior to testing, the sample was isotopically exchanged with deuterium to reduce residual tritium and passivated with air to alleviate pyrophoric concerns associated with handling the material outside of an inert glovebox. Analyses indicated that gas release from this sample was bimodal, with peaks near 220 and 490 C. degrees. The first peak consisted of both {sup 3}He and residual hydrogen isotopes, the second was primarily {sup 3}He. The bulk of the gas was released by 600 Celsius degrees. (author)

Preliminary decay heat calculations for the fuel loaded irradiation loop device of the RMB multipurpose Brazilian reactor

Energy Technology Data Exchange (ETDEWEB)

Campolina, Daniel; Costa, Antonio Carlos L. da; Andrade, Edison P., E-mail: campolina@cdtn.br, E-mail: aclp@cdtn.br, E-mail: epa@cdtn.br [Centro de Desenvolvimento da Tecnologia Nuclear (SETRE/CDTN/CNEN-MG), Belo Horizonte, MG (Brazil). Servico de Tecnologia de Reatores

2017-07-01

The structuring project of the Brazilian Multipurpose Reactor (RMB) is responsible for meeting the capacity to develop and test materials and nuclear fuel for the Brazilian Nuclear Program. An irradiation test device (Loop) capable of performing fuel test for power reactor rods is being conceived for RMB reflector. In this work preliminary neutronic calculations have been carried out in order to determine parameters to the cooling system of the Loop basic design. The heat released as a result of radioactive decay of fuel samples was calculated using ORIGEN-ARP and it resulted less than 200 W after 1 hour of irradiation interruption. (author)

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.)

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

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)

Capture of Tritium Released from Cladding in the Zirconium Recycle Process

Energy Technology Data Exchange (ETDEWEB)

Spencer, Barry B [ORNL; Bruffey, Stephanie H [ORNL; DelCul, Guillermo Daniel [ORNL; Walker, Trenton Baird [ORNL

2016-08-31

Zirconium may be recovered from the Zircaloy® cladding of used nuclear fuel (UNF) for recycle or to reduce the quantities of high-level waste destined for a geologic repository. Recovery of zirconium using a chlorination process is currently under development at the Oak Ridge National Laboratory. The approach is to treat the cladding with chlorine gas to convert the zirconium in the alloy (~98 wt % of the alloy mass) to zirconium tetrachloride. A significant fraction of the tritium (0–96%) produced in nuclear fuel during irradiation may be found in zirconium-based cladding and could be released from the cladding when the solid matrix is destroyed by the chlorination reaction. To prevent uncontrolled release of radioactive tritium to other parts of the plant or to the environment, a method to recover the tritium may be required. The focus of this effort was to (1) identify potential methods for the recovery of tritium from the off-gas of the zirconium recycle process, (2) perform scoping tests on selected recovery methods using nonradioactive gas simulants, and (3) select a process design appropriate for testing on radioactive gas streams generated by the engineering-scale zirconium recycle demonstrations on radioactive used cladding.

Capture of Tritium Released from Cladding in the Zirconium Recycle Process

Energy Technology Data Exchange (ETDEWEB)

Bruffey, Stephanie H [ORNL; Spencer, Barry B [ORNL; DelCul, Guillermo Daniel [ORNL

2016-08-31

This report is issued as the first revision to FCRD-MRWFD-2016-000297. Zirconium may be recovered from the Zircaloy® cladding of used nuclear fuel (UNF) for recycle or to reduce the quantities of high-level waste destined for a geologic repository. Recovery of zirconium using a chlorination process is currently under development at the Oak Ridge National Laboratory. The approach is to treat the cladding with chlorine gas to convert the zirconium in the alloy (~98 wt % of the alloy mass) to zirconium tetrachloride. A significant fraction of the tritium (0–96%) produced in nuclear fuel during irradiation may be found in zirconium-based cladding and could be released from the cladding when the solid matrix is destroyed by the chlorination reaction. To prevent uncontrolled release of radioactive tritium to other parts of the plant or to the environment, a method to recover the tritium may be required. The focus of this effort was to (1) identify potential methods for the recovery of tritium from the off-gas of the zirconium recycle process, (2) perform scoping tests on selected recovery methods using non-radioactive gas simulants, and (3) select a process design appropriate for testing on radioactive gas streams generated by the engineering-scale zirconium recycle demonstrations on radioactive used cladding.

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

A tritium handling laboratory was constructed at the National Institute for Fusion Science about twenty years ago and it was recently closed down. We completed the necessary work that is legally required in Japan at the laboratory, when the use of radioisotopes is discontinued, involving measurements of radioactive contamination. We mainly used smear and direct-immersion methods for the measurements. In applying the smear method, we used a piece of filter paper to wipe up the tritium staining the surfaces. The filter paper containing the tritium was placed directly into a dedicated vial, a scintillation cocktail was then poured over it, and the tritium was measured with a liquid scintillation counter. With the direct-immersion method, a piece of concrete was placed directly into a vial containing a scintillation cocktail, and the tritium in the concrete was measured with a liquid scintillation counter. As well as these measurements, we investigated water-extraction and heating-cooling methods for measuring tritium contamination in concrete. With the former, a piece of concrete was placed into water in a tube to extract the tritium, the water containing the extracted tritium was then poured into a dedicated vial containing a scintillation cocktail, and the tritium contamination was measured. With the latter, a piece of concrete was placed into a furnace and heated to 800 degrees centigrade to vaporize the tritiated water into flowing dry air. The flowing air was then cooled to collect the vaporized tritiated water in a tube. The collected water was placed in a vial for scintillation counting. To evaluate the direct-immersion method, ratios were determined by dividing the contamination measured with the heating-cooling method by that measured with the direct-immersion method. The average ratio was about 2.5, meaning a conversion factor from contamination obtained with the direct-immersion method to that with the heating-cooling method. We also investigated the

Neutron irradiation effects on plasma facing materials

Science.gov (United States)

Barabash, V.; Federici, G.; Rödig, M.; Snead, L. L.; Wu, C. H.

2000-12-01

This paper reviews the effects of neutron irradiation on thermal and mechanical properties and bulk tritium retention of armour materials (beryllium, tungsten and carbon). For each material, the main properties affected by neutron irradiation are described and the specific tests of neutron irradiated armour materials under thermal shock and disruption conditions are summarized. Based on current knowledge, the expected thermal and structural performance of neutron irradiated armour materials in the ITER plasma facing components are analysed.

Neutron irradiation effects on plasma facing materials

International Nuclear Information System (INIS)

Barabash, V.; Federici, G.; Roedig, M.; Snead, L.L.; Wu, C.H.

2000-01-01

This paper reviews the effects of neutron irradiation on thermal and mechanical properties and bulk tritium retention of armour materials (beryllium, tungsten and carbon). For each material, the main properties affected by neutron irradiation are described and the specific tests of neutron irradiated armour materials under thermal shock and disruption conditions are summarized. Based on current knowledge, the expected thermal and structural performance of neutron irradiated armour materials in the ITER plasma facing components are analysed

Decay and Transmutation of Nuclides

CERN Document Server

Aarnio, Pertti A

1999-01-01

We present a computer code DeTra which solves analytically the Bateman equations governing the decay, build-up and transmutation of radionuclides. The complexity of the chains and the number of nuclides are not limited. The nuclide production terms considered include transmutation of the nuclides inside the chain, external production, and fission. Time dependent calculations are possible since all the production terms can be re-defined for each irradiation step. The number of irradiation steps and output times is unlimited. DeTra is thus able to solve any decay and transmutation problem as long as the nuclear data i.e. decay data and production rates, or cross sections, are known.

Properties of tritium and its compounds

International Nuclear Information System (INIS)

Belovodskij, L.F.; Gaevoj, V.K.; Grishmanovskij, V.I.

1985-01-01

Ways of tritium preparation and different aspects of its application are considered. Physicochemical properties of this isotope and some compounds of it - tritium oxides, lithium, titanium, zirconium, uranium tritides, tritium organic compounds - are discussed. In particular, diffusion of tritium and its oxide through different materials, tritium oxidation processes, decomposition of tritium-containing compounds under the action of self-radiation are considered. Main radiobiological tritium properties are described

Comparison of tritium production facilities

International Nuclear Information System (INIS)

He Kaihui; Huang Jinhua

2002-01-01

Detailed investigation and research on the source of tritium, tritium production facilities and their comparison are presented based on the basic information about tritium. The characteristics of three types of proposed tritium production facilities, i.e., fissile type, accelerator production tritium (APT) and fusion type, are presented. APT shows many advantages except its rather high cost; fusion reactors appear to offer improved safety and environmental impacts, in particular, tritium production based on the fusion-based neutron source costs much lower and directly helps the development of fusion energy source

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

ARIES-I tritium system

International Nuclear Information System (INIS)

Sze, D.K.; Tam, S.W.; Billone, M.C.; Hassanein, A.M.; Martin, R.

1990-09-01

A key safety concern in a D-T fusion reactor is the tritium inventory. There are three components in a fusion reactor with potentially large inventories, i.e., the blanket, the fuel processing system and the plasma facing components. The ARIES team selected the material combinations, decided the operating conditions and refined the processing systems, with the aiming of minimizing the tritium inventories and leakage. The total tritium inventory for the ARIES-I reactor is only 700 g. This paper discussed the calculations and assumptions we made for the low tritium inventory. We also addressed the uncertainties about the tritium inventory. 13 refs., 2 figs., 3 tabs

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

Tritium control in fusion reactor materials: A model for Tritium Extracting System

International Nuclear Information System (INIS)

Zucchetti, Massimo; Utili, Marco; Nicolotti, Iuri; Ying, Alice; Franza, Fabrizio; Abdou, Mohamed

2015-01-01

Highlights: • A modeling work has been performed to address these issues in view of its utilization for the TES (Tritium Extraction System), in the case of the HCPB TBM and for a Molecular sieve as adsorbent material. • A computational model has been setup and tested in this paper. • The results of experimental measurement of fundamental parameters such as mass transfer coefficients have been implemented in the model. • It turns out the capability to model the extraction process of gaseous tritium compounds and to estimate the breakthrough curves of the two main tritium gaseous species (H2 and HT). - Abstract: In fusion reactors, tritium is bred by lithium isotopes inside the blanket and then extracted. However, tritium can contaminate the reactor structures, and can be eventually released into the environment. Tritium in reactor components should therefore be kept under close control throughout the fusion reactor lifetime, bearing in mind the risk of accidents, the need for maintenance and the detritiation of dismantled reactor components before their re-use or disposal. A modeling work has been performed to address these issues in view of its utilization for the TES (Tritium Extraction System), in the case of the HCPB TBM and for a molecular sieve as adsorbent material. A computational model has been setup and tested. The results of experimental measurement of fundamental parameters such as mass transfer coefficients have been implemented in the model. It turns out the capability of the model to describe the extraction process of gaseous tritium compounds and to estimate the breakthrough curves of the two main tritium gaseous species (H2 and HT).

Tritium control in fusion reactor materials: A model for Tritium Extracting System

Energy Technology Data Exchange (ETDEWEB)

Zucchetti, Massimo [DENERG, Politecnico di Torino (Italy); Utili, Marco, E-mail: marco.utili@enea.it [ENEA UTIS – C.R. Brasimone, Bacino del Brasimone, Camugnano, BO (Italy); Nicolotti, Iuri [DENERG, Politecnico di Torino (Italy); Ying, Alice [University of California Los Angeles (UCLA), Los Angeles, CA (United States); Franza, Fabrizio [Karlsruhe Institute of Technology, Karlsruhe (Germany); Abdou, Mohamed [University of California Los Angeles (UCLA), Los Angeles, CA (United States)

2015-10-15

Highlights: • A modeling work has been performed to address these issues in view of its utilization for the TES (Tritium Extraction System), in the case of the HCPB TBM and for a Molecular sieve as adsorbent material. • A computational model has been setup and tested in this paper. • The results of experimental measurement of fundamental parameters such as mass transfer coefficients have been implemented in the model. • It turns out the capability to model the extraction process of gaseous tritium compounds and to estimate the breakthrough curves of the two main tritium gaseous species (H2 and HT). - Abstract: In fusion reactors, tritium is bred by lithium isotopes inside the blanket and then extracted. However, tritium can contaminate the reactor structures, and can be eventually released into the environment. Tritium in reactor components should therefore be kept under close control throughout the fusion reactor lifetime, bearing in mind the risk of accidents, the need for maintenance and the detritiation of dismantled reactor components before their re-use or disposal. A modeling work has been performed to address these issues in view of its utilization for the TES (Tritium Extraction System), in the case of the HCPB TBM and for a molecular sieve as adsorbent material. A computational model has been setup and tested. The results of experimental measurement of fundamental parameters such as mass transfer coefficients have been implemented in the model. It turns out the capability of the model to describe the extraction process of gaseous tritium compounds and to estimate the breakthrough curves of the two main tritium gaseous species (H2 and HT).

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

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

Tritium in precipitation of Vostok (Antarctica): conclusions on the tritium latitude effect.

Science.gov (United States)

Hebert, Detlef

2011-09-01

During the Antarctic summer of 1985 near the Soviet Antarctic station Vostok, firn samples for tritium measurements were obtained down to a depth of 2.40 m. The results of the tritium measurements are presented and discussed. Based on this and other data, conclusions regarding the tritium latitude effect are derived.

Tritium inventory tracking and management

International Nuclear Information System (INIS)

Eichenberg, T.W.; Klein, A.C.

1990-01-01

This investigation has identified a number of useful applications of the analysis of the tracking and management of the tritium inventory in the various subsystems and components in a DT fusion reactor system. Due to the large amounts of tritium that will need to be circulated within such a plant, and the hazards of dealing with the tritium an electricity generating utility may not wish to also be in the tritium production and supply business on a full time basis. Possible scenarios for system operation have been presented, including options with zero net increase in tritium inventory, annual maintenance and blanket replacement, rapid increases in tritium creation for the production of additional tritium supplies for new plant startup, and failures in certain system components. It has been found that the value of the tritium breeding ratio required to stabilize the storage inventory depends strongly on the value and nature of other system characteristics. The real operation of a DT fusion reactor power plant will include maintenance and blanket replacement shutdowns which will affect the operation of the tritium handling system. It was also found that only modest increases in the tritium breeding ratio are needed in order to produce sufficient extra tritium for the startup of new reactors in less than two years. Thus, the continuous operation of a reactor system with a high tritium breeding ratio in order to have sufficient supplies for other plants is not necessary. Lastly, the overall operation and reliability of the power plant is greatly affected by failures in the fuel cleanup and plasma exhaust systems

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

Hot muonic deuterium and tritium from cold targets

International Nuclear Information System (INIS)

Marshall, G.M.; Beveridge, J.L.; Bailey, J.M.; Beer, G.A.; Knowles, P.E.; Mason, G.R.; Olin, A.; Brewer, J.H.; Forster, B.M.; Huber, T.M.; Pippitt, B.; Jacot-Guillarmod, R.; Schellenberg, L.; Martoff, C.J.; Petitjean, C.

1992-01-01

Experiments are described which use a solid hydrogen layer to form muonic hydrogen isotopes in vacuum. The method relies on transfer of the muon from protium to either a deuteron or a triton. The resulting muonic deuterium or muonic tritium will not immediately thermalize because of the very low elastic cross sections, and may be emitted from the surface of the layer. Measurements which detect decay electrons, muonic x-rays, and fusion products have been used to study the processes. A target has been constructed which exploits muonic atom emission in order to study the energy dependence of transfer and muon molecular formation

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

Tritium metrology within different media: focus on organically bound tritium (OBT); Metrologie du tritium dans differentes matrices: cas du tritium organiquement lie (TOL)

Energy Technology Data Exchange (ETDEWEB)

Baglan, N. [CEA Bruyeres-le-Chatel, DIF, 91 (France); Ansoborlo, E. [CEA Marcoule, DEN/DRCP/CETAMA, 30 (France); Cossonnet, C. [IRSN, DEI/STEME/LMRE, 91 - Orsay (France); Fouhal, L. [CEA Cadarache, DEN/D2S/LANSE, 13 - Saint-Paul-lez-Durance (France); Deniau, I.; Mokili, M. [SUBATECH/IN2P3/CNRS, 44 - Nantes (France); Henry, A. [AREVA-NC/DQSSE/PR - La Hague, 50 - Beaumont-Hague, (France); Fourre, E. [CEA Saclay, DSM/DRECAM/LSCE, 91 - Gif-sur-Yvette (France); Olivier, A. [GEA-Marine nationale, 50 - Cherbourg (France)

2010-07-15

The measurement of tritium in its various forms (mainly gas (HT), water (HTO) or solid (hydrides)), is an important key step for evaluating health and environmental risks and finally, dosimetry assessment. In vegetable or animal samples, tritium is often associated with the free water fraction, but may be included in the organic form as organically bound tritium (OBT). In this case, 2 forms exist: (i) a fraction called exchangeable or labile (E-OBT), bound to oxygen and nitrogen atoms, and (ii) a so-called non-exchangeable fraction (NE-OBT) bound to carbon atoms. The main technique for tritium analysis is liquid scintillation, which enables one to measure concentrations in the range of several Bq.L{sup -1}. The standards (AFNOR, ISO) published to date relate only to tritium analysis in water. Only one CETAMA method addresses OBT analysis in biological environments. This method has been tested since 2001 through intercomparison circuits on grass samples collected from the environment. Regarding tritium analysis in water, the strengths are reliability of this analysis at low concentrations (order of Bq.L{sup -1}), robustness and simplicity, and weaknesses are linked to problems of background, conservation and contamination of samples. Concerning OBT analysis, the analysis is reliable for values around 50 Bq.kg{sup -1} of fresh sample. The weaknesses are problems of contamination, reproducibility, analysis time (2 to 6 days) and lack of reference materials. The difficulty to date is the separation between E-OBT and NE-OBT, that will need experimental validation. (authors)

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.)

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)

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.)

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%

Tritium release of titan-tritium layers in air, aqueous solutions and living organisms of animals

International Nuclear Information System (INIS)

Biro, J.; Feher, I.; Mate, L.; Varga, L.

1978-01-01

Samples containing 400-1100 MBq (10-30 mCi) tritium were prepared and the effect of storage time on tritium release was followed. In 250 days one thousandth of the tritium was released in aqueous solution; in air the ratio of release per hour fell in the range of 10 -6 -10 -7 . Ti-T plates with different storage times were surgically placed in the abdomen of rats. Their tritium release dropped with time and the activity appearing in the circulation was lower than that of plates with 5-6 orders of magnitude. Checking the tritium incorporation of neutron generator operators it must be held in mind that only a minor part of tritium can be detected by the measurement of the tritium content of urine. (author)

Development of a tritium monitor combined with an electrochemical tritium pump using a proton conducting oxide

Energy Technology Data Exchange (ETDEWEB)

Tanaka, M. [National Institute for Fusion Science, Toki, Gifu (Japan); Sugiyama, T. [Nagoya University, Fro-cho, Chikusa-ku, Nagoya (Japan)

2015-03-15

The detection of low level tritium is one of the key issues for tritium management in tritium handling facilities. Such a detection can be performed by tritium monitors based on proton conducting oxide technique. We tested a tritium monitoring system composed of a commercial proportional counter combined with an electrochemical hydrogen pump equipped with CaZr{sub 0.9}In{sub 0.1}O{sub 3-α} as proton conducting oxide. The hydrogen pump operated at 973 K under electrolysis conditions using tritiated water vapor (HTO). The proton conducting oxide extracts tritium molecules (HT) from HTO and tritium concentration is measured by the proportional counter. The advantage of the proposed tritium monitoring system is that it is able to convert HTO into molecular hydrogen.

Tritium distribution between the fuel can and the oxide of fuel elements of light-water reactors

International Nuclear Information System (INIS)

Masson, M.

1986-12-01

The study on the measurement of tritium and other radionuclide contained in zircaloy fuel cans of the water cooled reactor fuel elements had two aims: the first was to estimate with accuracy the distribution of tritium in a fuel element (can + oxide). The measurement of tritium in the zircaloy fuel cans of the BORSSELE fuel elements associated with the measurement of tritium in the oxide allowed the establishment of a complete tritium balance on an industrial spent fuel element. This result has been compared to the values calculated by the code CEA/SEN and will allow to validate or adjust this calculation. The second aim delt with the characterization of the other radionuclides gaseous (Kr85) or not (Cs 134 and 137) contained in the solid zircaloy wastes (hulls) coming from the industrial reprocessing of ''water cooled'' fuel elements. These activity measurements in the hulls allowed to estimate the residual content of tritium, Kr 85 and other radionuclides which may be found in these solid wastes (high-level βγ radioactive wastes). Original experimental methods have been developed to reach these aims (dissolution in ammonium bifluoride medium and quantitative recovery of gases produced, radiochromatography, and liquid scintillation after double distillation). One tries to explain the presence of Kr 85 in the irradiated can [fr

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.)

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

TFTR tritium operations lessons learned

International Nuclear Information System (INIS)

Gentile, C.A.; Raftopoulos, S.; LaMarche, P.

1996-01-01

The Tokamak Fusion Test Reactor which is the progenitor for full D-T operating tokamaks has successfully processed > 81 grams of tritium in a safe and efficient fashion. Many of the fundamental operational techniques associated with the safe movement of tritium through the TFTR facility were developed over the course of many years of DOE tritium facilities (LANL, LLNL, SRS, Mound). In the mid 1980's The Tritium Systems Test Assembly (TSTA) at LANL began reporting operational techniques for the safe handling of tritium, and became a major conduit for the transfer of safe tritium handling technology from DOE weapons laboratories to non-weapon facilities. TFTR has built on many of the TSTA operational techniques and has had the opportunity of performing and enhancing these techniques at America's first operational D-T fusion reactor. This paper will discuss negative pressure employing 'elephant trunks' in the control and mitigation of tritium contamination at the TFTR facility, and the interaction between contaminated line operations and Δ pressure control. In addition the strategy employed in managing the movement of tritium through TFTR while maintaining an active tritium inventory of < 50,000 Ci will be discussed. 5 refs

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.

Tritium in plants; Le tritium dans la matiere organique des vegetaux

Energy Technology Data Exchange (ETDEWEB)

Vichot, L.; Losset, Y. [CEA Valduc, 21 - Is-sur-Tille (France)

2009-07-01

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.)

Exploration for tritium-free water

International Nuclear Information System (INIS)

Hussain, S.D.

1982-10-01

Tritium-free water is generally required in large quantities for the preparation of laboratory tritium standards as well as blanks which are used to determine background count rate in the measurement of low level tritium concentrations in water samples by liquid scintillation counting method. In order to meet the requirements of tritium-free water and save the recurring expenditure on its import from abroad, exploration for locating its source in the country was undertaken. Water samples collected from a few possible sources were analysed precisely for their tritium content at the International Atomic Energy Agency, Vienna, Austria and a source of tritium-free water was determined. (authors)

Tritium as tracer of groundwater pollution extension: case study of Andralanitra landfill site, Antananarivo-Madagascar

Science.gov (United States)

Ramaroson, Voahirana; Rakotomalala, Christian Ulrich; Rajaobelison, Joel; Fareze, Lahimamy Paul; Razafitsalama, Falintsoa A.; Rasolofonirina, Mamiseheno

2018-05-01

This study aims to understand the extension of groundwater pollution downstream of a landfill, Andralanitra-Antananarivo-Madagascar. Twenty-one samples, composed of dug well waters, spring waters, river, and lake, were measured in stable isotopes ( δ 2H, δ 18O) and tritium. Results showed that only two dug well waters, collected at the immediate vicinity of the landfill, have high tritium activities (22.82 TU and 10.43 TU), probably of artificial origin. Both upstream and further downstream of the landfill, tritium activities represent natural source, with values varying from 0.17 TU to 1.46 TU upstream and from 0.88 TU to 1.88 TU further downstream. Stable isotope data suggest that recharge occurs through infiltration of slightly evaporated rainfall. Using the radioactive decay equation, the calculated tracer ages related to two recent ground water samples collected down gradient of the landfill lay between [8-15] years and [4-7] years, taking into account the uncertainty of tritium measurements. For the calculation, a value of 2.36 TU was taken as A o. The latter was estimated based on similarity between stable isotope compositions of nearby spring and dug well waters as well as tritium activities of the local precipitation. Calculation of the tritium activities from the contaminated water point having 22.82 TU to further downstream using the calculated tracer ages showed values of one order of magnitude higher than the measured values. The absence of hydrological connection from the contaminated water point to further downstream the landfill would explain the lower tritium activities measured. Groundwater pollution seems to be limited to the closest proximity of the landfill.

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

Behavior of beryllium pebbles under irradiation

Energy Technology Data Exchange (ETDEWEB)

Dalle-Donne, M.; Scaffidi-Argentina, F. [Forschungszentrum Karlsruhe GmbH Technik und Umwelt (Germany). Inst. fuer Neutronenphysik und Reactortechnik; Baldwin, D.L.; Gelles, D.S.; Greenwood, L.R.; Kawamura, H.; Oliver, B.M.

1998-01-01

Beryllium pebbles are being considered in fusion reactor blanket designs as neutron multiplier. An example is the European `Helium Cooled Pebble Bed Blanket.` Several forms of beryllium pebbles are commercially available but little is known about these forms in response to fast neutron irradiation. Commercially available beryllium pebbles have been irradiated to approximately 1.3 x 10{sup 22} n/cm{sup 2} (E>1 MeV) at 390degC. Pebbles 1-mm in diameter manufactured by Brush Wellman, USA and by Nippon Gaishi Company, Japan, and 3-mm pebbles manufactured by Brush Wellman were included. All were irradiated in the below-core area of the Experimental Breeder Reactor-II in Idaho Falls, USA, in molybdenum alloy capsules containing helium. Post-irradiation results are presented on density change measurements, tritium release by assay, stepped-temperature anneal, and thermal ramp desorption tests, and helium release by assay and stepped-temperature anneal measurements, for Be pebbles from two manufacturing methods, and with two specimen diameters. The experimental results on density change and tritium and helium release are compared with the predictions of the code ANFIBE. (author)

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

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.

Technology developments for improved tritium management

International Nuclear Information System (INIS)

Miller, J.M.; Spagnolo, D.A.

1994-06-01

Tritium technology developments have been an integral part of the advancement of CANDU reactor technology. An understanding of tritium behaviour within the heavy-water systems has led to improvements in tritium recovery processes, tritium measurement techniques and overall tritium control. Detritiation technology has been put in place as part of heavy water and tritium management practices. The advances made in these technologies are summarized. (author). 20 refs., 5 figs

Operation of the tokamak fusion test reactor tritium systems during initial tritium experiments

International Nuclear Information System (INIS)

Anderson, J.L.; Gentile, C.; Kalish, M.; Kamperschroer, J.; Kozub, T.; LaMarche, P.; Murray, H.; Nagy, A.; Raftopoulos, S.; Rossmassler, R.; Sissingh, R.; Swanson, J.; Tulipano, F.; Viola, M.; Voorhees, D.; Walters, R.T.

1995-01-01

The high power D-T experiments on the tokamak fusion test reactor (TFTR) at the Princeton Plasma Physics Laboratory commenced in November 1993. During initial operation of the tritium systems a number of start-up problems surfaced and had to be corrected. These were corrected through a series of system modifications and upgrades and by repair of failed or inadequate components. Even as these operational concerns were being addressed, the tritium systems continued to support D-T operations on the tokamak. During the first six months of D-T operations more than 107kCi of tritium were processed successfully by the tritium systems. D-T experiments conducted at TFTR during this period provided significant new data. Fusion power in excess of 9MW was achieved in May 1994. This paper describes some of the early start-up issues, and reports on the operation of the tritium system and the tritium tracking and accounting system during the early phase of TFTR D-T experiments. (orig.)

Tritium emissions from a detritiation facility

International Nuclear Information System (INIS)

Rodrigo, L.; El-Behairy, O.; Boniface, H.; Hotrum, C.; McCrimmon, K.

2010-01-01

Tritium is produced in heavy-water reactors through neutron capture by the deuterium atom. Annual production of tritium in a CANDU reactor is typically 52-74 TBq/MW(e). Some CANDU reactor operators have implemented detritiation technology to reduce both tritium emissions and dose to workers and the public from reactor operations. However, tritium removal facilities also have the potential to emit both elemental tritium and tritiated water vapor during operation. Authorized releases to the environment, in Canada, are governed by Derived Release Limits (DRLs). DRLs represent an estimate of a release that could result in a dose of 1 mSv to an exposed member of the public. For the Darlington Nuclear Generating Station, the DRLs for airborne elemental tritium and tritiated water emissions are ~15.6 PBq/week and ~825 TBq/week respectively. The actual tritium emissions from Darlington Tritium Removal Facility (DTRF) are below 0.1% of the DRL for elemental tritium and below 0.2% of the DRL for tritiated water vapor. As part of an ongoing effort to further reduce tritium emissions from the DTRF, we have undertaken a review and assessment of the systems design, operating performance, and tritium control methods in effect at the DTRF on tritium emissions. This paper discusses the results of this study. (author)

Formation of radiation-induced defects and their influence on tritium extraction from lithium silicates in out-of-pile experiments

International Nuclear Information System (INIS)

Abramenkovs, A.A.; Tiliks, J.E.

1991-01-01

Formation and properties of radiation-induced defects and radiolysis products in lithium silicates irradiated in nuclear reactor till absorbed doses 1000 MGy were studied. Radiation-induced defects (RD) and radiolysis products (RP) were qualitatively and quantitatively determinated by methods of chemical scavengers (MHS), electron-spin resonance (ESR) and optical spectroscopy. Colloidal silicon and lithium, lithium and silicon oxides, oxygen, silicon and lithium peroxides are the final products of the lithium silicates radiolysis at absorbed energy doses D abs = 1000 MGy. The concentration of radiation defects and products of radiolysis strongly depend on the temperature of irradiation, humidity, granural size. The thermostimulated extraction of tritiated water (95-98% of the released tritium is in chemical form of water) from lithium silicates ceramics proceeds according to two independent mechanisms: a) chemidesorption of surface localized tritiated water (the first order chemical reaction); b) formation of the tritium water molecules limited by triton diffusion to the near-surface layer of grains. It has been found that the concentration of radiation-induced defects considerably affects the tritium localization and releasing processes from lithium silicates. (orig.)

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

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)

Present status and program of radiobiological tritium research in Japan

International Nuclear Information System (INIS)

Tazima, Y.

1981-01-01

Recent projects of the study on the biological effects of tritium in Japan, were reviewed. The investigations were about the behavior of tritium in food chain, i.e., intake to organ or tissue, retention, and distribution, and in genetic stage. As an example RBE studies on the induction of mutations in the silkworm and on transforming were described. Tritiated water was injected into wild type female pupae and radiation dose-rate was calculated from the radioactivity transmitted to the deposited eggs. γ-ray irradiation was carried out, in parallel, at approximately similar dose rates. RBE of THO for mutation fell between 1 and 2. The experiments with transforming principle of B. subtilis showed that the treatment of the bacterial spore with 3 H-glycelin or 3 H-water derived more inactive transformation with the decrease of the concentrations. (Nakanishi, T.)

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

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.)

Tritium containing polymers having a polymer backbone substantially void of tritium

Science.gov (United States)

Jensen, G.A.; Nelson, D.A.; Molton, P.M.

1992-03-31

A radioluminescent light source comprises a solid mixture of a phosphorescent substance and a tritiated polymer. The solid mixture forms a solid mass having length, width, and thickness dimensions, and is capable of self-support. In one aspect of the invention, the phosphorescent substance comprises solid phosphor particles supported or surrounded within a solid matrix by a tritium containing polymer. The tritium containing polymer comprises a polymer backbone which is essentially void of tritium. 2 figs.

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.)

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

Overview of tritium fast-fission yields

International Nuclear Information System (INIS)

Tanner, J.E.

1981-03-01

Tritium production rates are very important to the development of fast reactors because tritium may be produced at a greater rate in fast reactors than in light water reactors. This report focuses on tritium production and does not evaluate the transport and eventual release of the tritium in a fast reactor system. However, if an order-of-magnitude increase in fast fission yields for tritium is confirmed, fission will become the dominant production source of tritium in fast reactors

Tritium in rad waste management

International Nuclear Information System (INIS)

Gandhi, P.M.; Ali, S.S.; Mathur, R.K.; Rastogi, R.C.

1990-01-01

Radioactive waste arising from PHWR's are invariably contaminated with tritium activity. Their disposal is crucial as it governs the manner and extent of radioactive contamination of human environment. The technique of tritium measurement and its application plays an important role in assessing the safety of the disposal system. Thus, typical applications involving tritium measurements include the evaluation of a site for solid waste burial facility and evaluation of a water body for liquid waste dispersal. Tritium measurement is also required in assessing safe air route dispersal of tritium. (author)

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)

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.

The Chalk River Tritium Extraction Plant

International Nuclear Information System (INIS)

Holtslander, W.J.; Harrison, T.E.; Spagnolo, D.A.

1990-01-01

The Chalk River Tritium Extraction Plant for removal of tritium from heavy water is described. Tritium is present in the heavy water from research reactors in the form of DTO at a concentration in the range of 1-35 Ci/kg. It is removed by a combination of catalytic exchange to transfer the tritium from DTO to DT, followed by cryogenic distillation to separate and concentrate the tritium to T 2 . The tritium product is reacted with titanium and packaged for transportation and storage as titanium tritide. The plant processes heavy water at a rate of 25 kg/h and removes 80% of the tritium and 90% of the protium per pass. Catalytic exchange is carried out in the liquid phase using a proprietary wetproofed catalyst. The plant serves two roles in the Canadian fusion program: it produces pure tritium for use in fusion research and development, and it demonstrates on an industrial scale many of the tritium technologies that are common to the tritium systems in fusion reactors (author)

The Chalk River Tritium Extraction Plant

Energy Technology Data Exchange (ETDEWEB)

Holtslander, W J; Harrison, T E; Spagnolo, D A

1990-07-01

The Chalk River Tritium Extraction Plant for removal of tritium from heavy water is described. Tritium is present in the heavy water from research reactors in the form of DTO at a concentration in the range of 1-35 Ci/kg. It is removed by a combination of catalytic exchange to transfer the tritium from DTO to DT, followed by cryogenic distillation to separate and concentrate the tritium to T{sub 2}. The tritium product is reacted with titanium and packaged for transportation and storage as titanium tritide. The plant processes heavy water at a rate of 25 kg/h and removes 80% of the tritium and 90% of the protium per pass. Catalytic exchange is carried out in the liquid phase using a proprietary wetproofed catalyst. The plant serves two roles in the Canadian fusion program: it produces pure tritium for use in fusion research and development, and it demonstrates on an industrial scale many of the tritium technologies that are common to the tritium systems in fusion reactors (author)

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

Tritium metabolism in cow's milk after administration of tritiated water and of organically bound tritium

International Nuclear Information System (INIS)

Hoek, J. van den

1982-01-01

Tritium was administered as THO and as organically bound tritium (OBT) to lactating cows. Urine and milk samples were collected and analyzed for tritium content. Plateau levels in milk water and in milk fat, lactose and casein were reached in about 20 days after feeding either THO or OBT. Comparison of the specific activity (pCi 3 H/g H) of the various milk constituents with the specific activity of the body water showed that, after administration of THO, the highest tritium incorporation occurred in lactose (0.58), followed by milk fat (0.36) and casein (0.27). Tritium incorporation in milk dry matter (0.45) is considerably higher than in most tissue components of several mammalian species after continuous ingestion of THO as reported in the literature. After feeding OBT, the highest tritium incorporation occurred in milk fat and to a lesser extent in casein. Tritium levels in lactose were surprisingly low and the reason for this is not clear. They were similar to those in milk water. Tritium levels in milk and urine water showed systematic differences during administration of OBT and after this was stopped. There was more tritium in milk water until the last day of OBT feeding and this situation was reversed after this. (author)

Tritium metabolism in cow's milk after administration of tritiated water and of organically bound tritium

Energy Technology Data Exchange (ETDEWEB)

van den Hoek, J [Landbouwhogeschool Wageningen (Netherlands). Lab. voor Fysiologie der Dieren; Gerber, G; Kirchmann, R [Centre d' Etude de l' Energie Nucleaire, Mol (Belgium)

1982-01-01

Tritium was administered as THO and as organically bound tritium (OBT) to lactating cows. Urine and milk samples were collected and analyzed for tritium content. Plateau levels in milk water and in milk fat, lactose and casein were reached in about 20 days after feeding either THO or OBT. Comparison of the specific activity (pCi/sup 3/H/g H) of the various milk constituents with the specific activity of the body water showed that, after administration of THO, the highest tritium incorporation occurred in lactose (0.58), followed by milk fat (0.36) and casein (0.27). Tritium incorporation in milk dry matter (0.45) is considerably higher than in most tissue components of several mammalian species after continuous ingestion of THO as reported in the literature. After feeding OBT, the highest tritium incorporation occurred in milk fat and to a lesser extent in casein. Tritium levels in lactose were surprisingly low and the reason for this is not clear. They were similar to those in milk water. Tritium levels in milk and urine water showed systematic differences during administration of OBT and after this was stopped. There was more tritium in milk water until the last day of OBT feeding and this situation was reversed after this.

How to improve the irradiation conditions for the International Fusion Materials Irradiation Facility

CERN Document Server

Daum, E

2000-01-01

The accelerator-based intense D-Li neutron source International Fusion Materials Irradiation Facility (IFMIF) provides very suitable irradiation conditions for fusion materials development with the attractive option of accelerated irradiations. Investigations show that a neutron moderator made of tungsten and placed in the IFMIF test cell can further improve the irradiation conditions. The moderator softens the IFMIF neutron spectrum by enhancing the fraction of low energy neutrons. For displacement damage, the ratio of point defects to cascades is more DEMO relevant and for tritium production in Li-based breeding ceramic materials it leads to a preferred production via the sup 6 Li(n,t) sup 4 He channel as it occurs in a DEMO breeding blanket.

Tritium loss in molten flibe systems

Energy Technology Data Exchange (ETDEWEB)

Longhurst, G.R.; Anderl, R.A. [Idaho National Eng. and Environ. Lab., Idaho Falls, ID (United States); Scott Willms, R. [Los Alamos National Lab., NM (United States)

2000-04-01

An emerging issue relative to beryllium technology in fusion involves tritium interactions with molten beryllium-bearing salts. Innovative designs for fusion reactors, both magnetic and inertially confined, feature the molten salt mixture 2LiF.BeF{sub 2}, commonly called Flibe, as a tritium breeder and coolant. Tritium is bred in the Flibe as neutrons from the plasma are absorbed by Li atoms, which then transmute to tritium and helium. Transmutation of tritium from Be also occurs. Among the issues to be resolved for such coolant systems is the potential loss of tritium from the Flibe coolant to the walls of the system, particularly through heat exchanger tubes, and from there into secondary coolants or working fluids and the environment. Effectively removing tritium from Flibe in clean-up units is also important. In quiescent or low Reynolds number flow, tritium movement through Flibe is governed by diffusion. For Flibe in turbulent flow, as in heat exchanger tubes, transport is by turbulent mixing, and the same flow conditions and structural design features that maximize heat transfer to the heat exchanger walls will enhance the transport of tritium to those same surfaces. Analyses have been performed to estimate the fractional loss of tritium through heat exchanger tubes and release rates from Flibe droplets in vacuum disengagers in molten Flibe systems. The calculations suggest unacceptably large losses of tritium through heat exchanger tubes. The gravity of the implications of these estimates calls for experimental verification to determine if tritium losses through molten Flibe heat exchangers or other Flibe systems can really be so high and whether vacuum disengagers will really work. There is also a need for better information on evolution of tritium from Flibe droplets in a vacuum. Several experiments are presently being planned to address these issues and are discussed. These include experiments to induce tritium in Flibe using spontaneous fission neutrons

Tritium resources available for fusion reactors

Science.gov (United States)

Kovari, M.; Coleman, M.; Cristescu, I.; Smith, R.

2018-02-01

The tritium required for ITER will be supplied from the CANDU production in Ontario, but while Ontario may be able to supply 8 kg for a DEMO fusion reactor in the mid-2050s, it will not be able to provide 10 kg at any realistic starting time. The tritium required to start DEMO will depend on advances in plasma fuelling efficiency, burnup fraction, and tritium processing technology. It is in theory possible to start up a fusion reactor with little or no tritium, but at an estimated cost of 2 billion per kilogram of tritium saved, it is not economically sensible. Some heavy water reactor tritium production scenarios with varying degrees of optimism are presented, with the assumption that only Canada, the Republic of Korea, and Romania make tritium available to the fusion community. Results for the tritium available for DEMO in 2055 range from zero to 30 kg. CANDU and similar heavy water reactors could in theory generate additional tritium in a number of ways: (a) adjuster rods containing lithium could be used, giving 0.13 kg per year per reactor; (b) a fuel bundle with a burnable absorber has been designed for CANDU reactors, which might be adapted for tritium production; (c) tritium production could be increased by 0.05 kg per year per reactor by doping the moderator with lithium-6. If a fusion reactor is started up around 2055, governments in Canada, Argentina, China, India, South Korea and Romania will have the opportunity in the years leading up to that to take appropriate steps: (a) build, refurbish or upgrade tritium extraction facilities; (b) extend the lives of heavy water reactors, or build new ones; (c) reduce tritium sales; (d) boost tritium production in the remaining heavy water reactors. All of the alternative production methods considered have serious economic and regulatory drawbacks, and the risk of diversion of tritium or lithium-6 would also be a major concern. There are likely to be serious problems with supplying tritium for future

Tritium loss in molten flibe systems

International Nuclear Information System (INIS)

Longhurst, G.R.; Anderl, R.A.; Scott Willms, R.

2000-01-01

An emerging issue relative to beryllium technology in fusion involves tritium interactions with molten beryllium-bearing salts. Innovative designs for fusion reactors, both magnetic and inertially confined, feature the molten salt mixture 2LiF.BeF 2 , commonly called Flibe, as a tritium breeder and coolant. Tritium is bred in the Flibe as neutrons from the plasma are absorbed by Li atoms, which then transmute to tritium and helium. Transmutation of tritium from Be also occurs. Among the issues to be resolved for such coolant systems is the potential loss of tritium from the Flibe coolant to the walls of the system, particularly through heat exchanger tubes, and from there into secondary coolants or working fluids and the environment. Effectively removing tritium from Flibe in clean-up units is also important. In quiescent or low Reynolds number flow, tritium movement through Flibe is governed by diffusion. For Flibe in turbulent flow, as in heat exchanger tubes, transport is by turbulent mixing, and the same flow conditions and structural design features that maximize heat transfer to the heat exchanger walls will enhance the transport of tritium to those same surfaces. Analyses have been performed to estimate the fractional loss of tritium through heat exchanger tubes and release rates from Flibe droplets in vacuum disengagers in molten Flibe systems. The calculations suggest unacceptably large losses of tritium through heat exchanger tubes. The gravity of the implications of these estimates calls for experimental verification to determine if tritium losses through molten Flibe heat exchangers or other Flibe systems can really be so high and whether vacuum disengagers will really work. There is also a need for better information on evolution of tritium from Flibe droplets in a vacuum. Several experiments are presently being planned to address these issues and are discussed. These include experiments to induce tritium in Flibe using spontaneous fission neutrons

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.)

Irradiation behaviour of a tritium breeding material, γ-LiAlO 2- results of two in-pile experiments: ALICE I and ALICE II

Science.gov (United States)

Botter, F.; Rasneur, B.; Roth, E.

1988-11-01

γ-LiAlO 2 has been studied at CEA as potential breeder material for fusion reactors within the scope of the EEC fusion technology program. Radiation damage was investigated by irradiating unclad aluminate samples in the core of the OSIRIS reactor at Saclay. As part of the international breeder material comparison program named BEATRIX, US samples were irradiated along with those prepared in Saclay; samples of natural 6Li content and 96% enriched ones were irradiated. Shapes were chosen to enable postirradiation examinations (PIE), and microstructures were optimized for tritium release. The ALICE 1 experiment was carried out during 25.7 full power days (FPD), ALICE II lasted 36.3 FPD. Temperatures ranged from 400 to 600°C in the first, from 750 to 850°C in the second ALICE irradiation (sample core temperatures). In both cases the maximum flux on the samples was 2.1 × 10 18n m -2 s -1 fast, and 0.7 × 10 18n m -2 s -2 thermal Power dissipated was up to 100 W/cm 3, higher than the average in most reactor blanket designs by a factor 3 to 10, thus enabling the highest burn-ups to correspond to more than two years of possible operation in a full-scale reactor. In the lower temperature range of irradiation no significant damage was observed. In the higher one shrinkage due to sintering was induced. Whatever the microstructure, the flux and temperature, all samples (but one) not exceeding 5 mm diameter and length were mechanically intact. Above those dimensions cracking, which can be assigned to excessive thermal stress, could be observed. Given anticipated operating conditions of blankets being designed, the behaviour of γ-LiAlO 2 under irradiation is that of a very promising material.

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