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Sample records for p-10 tritium separation

  1. Separation of Tritium from Wastewater

    International Nuclear Information System (INIS)

    JEPPSON, D.W.

    2000-01-01

    A proprietary tritium loading bed developed by Molecular Separations, Inc (MSI) has been shown to selectively load tritiated water as waters of hydration at near ambient temperatures. Tests conducted with a 126 (micro)C 1 tritium/liter water standard mixture showed reductions to 25 (micro)C 1 /L utilizing two, 2-meter long columns in series. Demonstration tests with Hanford Site wastewater samples indicate an approximate tritium concentration reduction from 0.3 (micro)C 1 /L to 0.07 (micro)C 1 /L for a series of two, 2-meter long stationary column beds Further reduction to less than 0.02 (micro)C 1 /L, the current drinking water maximum contaminant level (MCL), is projected with additional bed media in series. Tritium can be removed from the loaded beds with a modest temperature increase and the beds can be reused Results of initial tests are presented and a moving bed process for treating large quantities of wastewaters is proposed. The moving bed separation process appears promising to treat existing large quantities of wastewater at various US Department of Energy (DOE) sites. The enriched tritium stream can be grouted for waste disposition. The separations system has also been shown to reduce tritium concentrations in nuclear reactor cooling water to levels that allow reuse. Energy requirements to reconstitute the loading beds and waste disposal costs for this process appear modest

  2. 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)

  3. 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)

  4. Separation of tritium from other hydrogen isotopes

    International Nuclear Information System (INIS)

    Roth, E.

    1988-01-01

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

  5. Environmental monitoring for 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 within 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 almost all the neighbors of the Experimental Cryogenic Pilot are chemical plants. It is necessary to emphasize this aspect because the sewage system is connected with the other tree chemical plants from the 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 and waste water. The tritium level was between 10 TU and 27 TU what indicates that there is no sources 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 the standard method used for tritium determination in water samples, the precautions needed in order to achieve reliable results, and the evolution of tritium level in different location near the Tritium and Deuterium Cryogenic Separation Experimental Pilot. (authors)

  6. Tritium monitoring in environment at ICIT Tritium Separation Facility

    International Nuclear Information System (INIS)

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

    2008-01-01

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

  7. Separation of tritium from reprocessing effluents

    International Nuclear Information System (INIS)

    Bruggeman, A.; Doyen, W.; Harnie, R.; Leysen, R.; Meynendonckx, L.; Monsecour, M.; Goossens, W.R.A.; Baetsle, L.H.

    1980-01-01

    For several years tritium retention has been studied at the Belgian Nuclear Research Centre, SCK/CEN; initially attention was focused on the removal of tritium from gaseous reprocessing effluents. If tritium can be released from the spent fuel into the gaseous phase before any aqueous operation, adsorption on molecular sieves after some isotopic dilution with hydrogen and after complete conversion to (tritiated) water is the most practical collection method. A once-through 15 m 3 .h -1 oxidation-adsorption unit with a closed regeneration system and with a decontamination factor of 1000 at total (tritiated) hydrogen and water inlet concentrations down to 1000 vpm (parts per million by volume) has been constructed and tested at SCK/CEN and it is described in the text. If no special head-end treatment is used an appropriate liquid management inside the reprocessing plant restricts the volume of tritiated aqueous effluents to about 3 m 3 per tonne of LWR fuel processed. However, for further reduction an isotope separation process becomes necessary. SCK/CEN is developing the ELEX process, which is a combination of water ELectrolysis and tritium EXchange between hydrogen and water, the exchange being promoted by a hydrophobic catalyst. For electrolysis under normal conditions an elementary tritium separation factor of 11.6 with a standard deviation of 6% was obtained. As concerns the exchange step a hydrophobic catalyst has been developed which yields for the flow rates used at atmospheric pressure and at 20 0 C an overall exchange rate constant of 9 mol.s -1 .m -3 in a countercurrent trickle-bed reactor. At present an integrated bench scale de-tritiation unit is being built for further tests and for a dynamic demonstration of the ELEX process

  8. Separation of tritium from gaseous and aqueous effluent systems

    International Nuclear Information System (INIS)

    Kobisk, E.H.

    1977-01-01

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

  9. Tritium separation from heavy water using electrolysis

    International Nuclear Information System (INIS)

    Ogata, Y.; Sakuma, Y.; Ohtani, N.; Kodaka, M.

    2001-01-01

    A tritium separation from heavy water by the electrolysis using a solid polymer electrode (SPE) was specified on investigation. The heavy water (∼10 Bq g -1 ) and the light water (∼70 Bq g -1 ) were electrolysed using an electrolysis device (Tripure XZ001, Permelec Electrode Ltd.) with the SPE layer. The cathode was made of stainless steel (SUS314). The electrolysis was carried out at 20 A x 60 min, with the electrolysis temperature at 10, 20, or 30degC, and 15 A x 80 min at 5degC. The produced hydrogen and oxygen gases were recombined using a palladium catalyst (ND-101, N.E. Chemcat Ltd.) with nitrogen gas as a carrier. The activities of the water in the cell and of the recombined water were analyzed using a liquid scintillation counter. The electrolysis potential to keep the current 20 A was 2-3 V. The yields of the recombined water were more than 90%. The apparent separation factors (SF) for the heavy water and the light water were ∼2 and ∼12, respectively. The SF value was in agreement with the results in other work. The factors were changed with the cell temperature. The electrolysis using the SPE is applicable for the tritium separation, and is able to perform the small-scale apparatus at the room temperature. (author)

  10. Separation of tritium from aqueous effluents

    International Nuclear Information System (INIS)

    Geens, L.; Bruggeman, A.; Meynendonckx, L.; Parmentier, C.; Belien, H.; Ooms, E.; Smets, D.; Stevens, J.; van Vlerken, J.

    1988-01-01

    From 1975 until 1982 - within the framework of the CEC indirect action programme on management and storage of radioactive waste - the SCK/CEN has developed the ELEX process from laboratory scale experiments up to the construction of an integrated pilot installation. The ELEX process combines water electrolysis and catalytical isotope exchange for the separation of tritium from aqueous reprocessing effluents by isotope enrichment. Consequently, the pilot installation consists of two main parts: an 80 kW water electrolyser and a 10 cm diameter trickle bed exchange column. The feed rate of tritiated water amounts to 5 dm 3 .h -1 , containing up to 3.7 GBq.dm -3 of tritium. This report describes the further development of the process during the second phase of the second programme. Three main items are reported: (i) research work in the field of pretreatment of real reprocessing effluents, before feeding them to an ELEX installation; (ii) demonstration of the technical feasibility of the ELEX process with simulated active effluent streams in the pilot installation; (iii) a cost estimation for the ELEX installation, comprising the required investments and the annual operation costs

  11. Separation of hydrogen isotopes for tritium waste removal

    International Nuclear Information System (INIS)

    Wilkes, W.R.

    1975-01-01

    A distillation cascade for separating hydrogen isotopes was simulated by means of a multicomponent, multistage computer code. A hypothetical test mixture containing equal atomic fractions of protium, deuterium and tritium, equilibrated to high temperature molecular concentrations was used as feed. The results show that a two-column cascade can be used to separate the protium from the tritium. Deuterium appears both in the protium and the tritium product streams. (auth)

  12. Separation of tritium from aqueous effluents

    International Nuclear Information System (INIS)

    Bruggeman, A.; Leysen, R.; Meynendonckx, L.; Parmentier, C.; Bellien, H.; Smets, D.; Stevens, J.

    1984-01-01

    This report describes the further development of the so-called ELEX process, carried out from 1 July 1980 until 31 December 1982. The ELEX process is the combination of electrolysis with the catalytic tritium exchange between hydrogen and water in order to accumulate the tritium in the liquid phase. The experimental study of the catalytic tritium exchange between hydrogen and liquid water was continued and the overall exchange rate could be substantially increased. An alternative process based on bithermal exchange of tritium has been evaluated. In the 10 mol h -1 mini-pilot bench scale detritiation unit the ELEX process was successfully demonstrated by detritiating up to now more than 1m 3 of water containing up to 100 mCi tritium per dm 3 , which is the feed concentration to be expected for application of the process in a reprocessing plant. A 280 mol h -1 pilot detritiation installation now being constructed is described. This installation will realize a volume reduction factor of 100 and a process decontamination factor of 100. The maximum total tritium inventory will be about 1000 Ci. The plant consists mainly of a 80 kW electrolyser and a 10 cm diameter exchange column and can be considered as the ultimate step before industrial application of the ELEX process

  13. Separation of tritium from gaseous and aqueous effluent systems

    International Nuclear Information System (INIS)

    Kobisk, E.H.

    1977-01-01

    Removal or reduction of tritium content in a wide variety of effluent streams has been extensively studied in the United States. This paper specifically reviews three processes involving tritium separation in the gaseous phase and the aqueous phase. Diffusion through a selective Pd-25Ag alloy membrane at temperatures up to 600 0 C and at pressures up to 700 kg/cm 2 has resulted in successful separation of hydrogen-deuterium mixtures with an associated separation factor of 1.65 (and gives a calculated separation factor for hydrogen-tritium mixtures of 2.0). Use of a single palladium bipolar membrane in an electrolysis system has been found to yield a hydrogen-deuterium separation factor of 4 and a hydrogen-tritium factor of 6 to 11 without the production of gaseous hydrogen. Finally, countercurrent catalytic exchange between tritium-containing hydrogen gas and water has yielded a separation factor of 6.3. The specific advantages of each of these systems will be discussed in terms of their potential applications. In all cases, further investigations are necessary to scale the systems to handle large quantities of feed material in a continuous mode and to minimize energy requirements. Such separative systems must necessarily be cascaded to yield gaseous or aqueous product streams suitable for recycling to the tritium producing systems, for storage or for discharge to the environment. (orig./HP) [de

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

    International Nuclear Information System (INIS)

    Hayashi, Takumi; Okuno, Kenji

    1994-01-01

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

  15. Tissue free water tritium separation from foodstuffs by azeotropic distillation

    International Nuclear Information System (INIS)

    Constantin, F.; Ciubotaru, A.; Popa, D.

    1998-01-01

    In this paper the tritium separation from tissue free water in foodstuffs by azeotropic distillation is described. Tritium in tissue water is assayed by liquid scintillation counting using well-established quenched correction method. The mean value of the tritium concentration in tissue water from foodstuffs is about 6-12 Bq/l very similar to the tritium mean concentration measured in the surface waters of the area where the samples have been collected (about 12 Bq/l. Therefore, the tritium content in the water fraction of the food samples can be considered in equilibrium with the local environmental water sources. The azeotropic distillation it is an accessible separation method which does not need a sophisticated and expansive distillation apparatus. It is a fast method of separation tissue free water from foodstuffs being very important in the surveillance activity of the environmental within nuclear electric plant. It is suitable for processing a small quantity of samples and for a production type facility when a large number of samples must be processed because the solvent can be purified and reused. The azeotropic distillation has some limits being used to separate water from samples with high content of water (85-90%) and simple a simple chemical structures as: vegetables, fruits, cereal, soil, vegetation. According to the results obtained, the organic substituents of milk, wine, meat (casein, lactose, milk fat, alcohol, esters) may enhance the chemisorption of tritium on through exchange organic hydrogen as -OH, -SH, -NH, -COOH with tritium. Also, the tissue water separation by azeotropic distillation is not complete and can not guarantee the absence of the vaporization isotope effect of the HTO/H 2 O system., However, the azeotropic distillation is the preferred method of the water extraction from food samples, which makes it useful for the tritium transfer from soil to foodstuffs. (authors)

  16. Tissue free water tritium separation from foodstuffs by azeotropic distillation

    Energy Technology Data Exchange (ETDEWEB)

    Constantin, F; Ciubotaru, A; Popa, D [Inspectorate of Public Health of Bucharest (Romania)

    1999-12-31

    In this paper the tritium separation from tissue free water in foodstuffs by azeotropic distillation is described. Tritium in tissue water is assayed by liquid scintillation counting using well-established quenched correction method. The mean value of the tritium concentration in tissue water from foodstuffs is about 6-12 Bq/l very similar to the tritium mean concentration measured in the surface waters of the area where the samples have been collected (about 12 Bq/l. Therefore, the tritium content in the water fraction of the food samples can be considered in equilibrium with the local environmental water sources. The azeotropic distillation it is an accessible separation method which does not need a sophisticated and expansive distillation apparatus. It is a fast method of separation tissue free water from foodstuffs being very important in the surveillance activity of the environmental within nuclear electric plant. It is suitable for processing a small quantity of samples and for a production type facility when a large number of samples must be processed because the solvent can be purified and reused. The azeotropic distillation has some limits being used to separate water from samples with high content of water (85-90%) and simple a simple chemical structures as: vegetables, fruits, cereal, soil, vegetation. According to the results obtained, the organic substituents of milk, wine, meat (casein, lactose, milk fat, alcohol, esters) may enhance the chemisorption of tritium on through exchange organic hydrogen as -OH, -SH, -NH, -COOH with tritium. Also, the tissue water separation by azeotropic distillation is not complete and can not guarantee the absence of the vaporization isotope effect of the HTO/H{sub 2}O system., However, the azeotropic distillation is the preferred method of the water extraction from food samples, which makes it useful for the tritium transfer from soil to foodstuffs. (authors) 2 tabs.

  17. Tritium separation from light and heavy water by bipolar electrolysis

    International Nuclear Information System (INIS)

    Petek, M.; Ramey, D.W.; Taylor, R.D.

    1981-01-01

    Using multiple bipolar electrolytic separation of hydrogen isotopes with Pd-25%Ag electrodes, the mathematical feasibility of this method for tritium separation was shown and experimentally verified. Separation factors were measured on single bipolar electrodes and were found to be approximately equivalent to those associated with individual ordinary electrolytic systems. Multibipolar separations were experimentally achieved in single cascaded cells in which each bipolar electrode was of equal area to others in a series arrangement. Factors measured for multibipolar H-D separation were close to the values measured in single-stage cell measurements; for H-T separation, interstage leakage reduced the measured separation factor. However, in both cases separation of sufficient magnitude was achieved to show feasibility for real application to the extraction of tritium from large-volume systems at high current density. (author)

  18. ELEX process for tritium separation from aqueous effluents

    International Nuclear Information System (INIS)

    Bruggeman, A.; Doyen, W.; Leysen, R.; Meynendonckx, L.; Monsecour, M.; Goossens, W.R.A.

    1980-01-01

    Within the framework of the European Communities' indirect action program on management and storage of radioactive waste the Belgian Nuclear Research Centre, S.C.K./C.E.N., is developing the ELEX process for tritium separation from aqueous reprocessing effluents. This process is a combination of water electrolysis and tritium exchange between hydrogen and water, the exchange being promoted by a hydrophobic catalyst. For classical electrolysis under normal working conditions with elementary tritium separation factor of 11.6 with a standard deviation of 6% was obtained. As to the exchange step an appropriate hydrophobic catalyst has been developed, and overall tritium exchange rates were measured in a countercurrent packed-bed reactor. Extrapolation of these results to the 3 m 3 per day scale of a reprocessing plant leads to an electrolyser capacity of about 1 MW and to an exchange volume of about 1 m 3 for an ELEX installation that concentrates 90% of the original tritium in 1% of the original volume. At the moment the construction of a small integrated detritiation unit is nearly finished. A larger pilot installation will be built later on

  19. Tritium separation from light and heavy water by bipolar electrolysis

    International Nuclear Information System (INIS)

    Ramey, D.W.; Petek, M.; Taylor, R.D.; Kobisk, E.H.; Ramey, J.; Sampson, C.A.

    1979-10-01

    Use of bipolar electrolysis with countercurrent electrolyte flow to separate hydrogen isotopes was investigated for the removal of tritium from light water effluents or from heavy water moderator. Deuterium-tritium and protium-tritium separation factors occurring on a Pd-25% Ag bipolar electrode were measured to be 2.05 to 2.16 and 11.6 to 12.4 respectively, at current densities between 0.21 and 0.50 A cm -2 , and at 35 to 90 0 C. Current densities up to 0.3 A cm -2 have been achieved in continuous operation, at 80 to 90 0 C, without significant gas formation on the bipolar electrodes. From the measured overvoltage at the bipolar electrodes and the electrolyte conductivity the power consumption per stage was calculated to be 3.0 kwh/kg H 2 O at 0.2 A cm -2 and 5.0 kwh/kg H 2 O at 0.5 A cm -2 current density, compared to 6.4 and 8.0 kwh/kg H 2 O for normal electrolysis. A mathematical model derived for hydrogen isotope separation by bipolar electrolysis, i.e., for a square cascade, accurately describes the results for protium-tritium separation in two laboratory scale, multistage experiments with countercurrent electrolyte flow; the measured tiritum concentration gradient through the cascade agreed with the calculated values

  20. Tritium separation factors in distillation and chemical exchange processes

    International Nuclear Information System (INIS)

    Dave, S.M.; Ghosh, S.K.; Sadhukhan, H.K.

    1982-01-01

    The vapour pressures of different isotopic hydrogen, water and ammonia molecules have been calculated. These vapour pressures can be used to evaluate relative volatilities of different species for separation of tritium isotopes by distillation. The equilibrium constants for various exchange reactions involving different deuterated and tritiated species of hydrogen, water and ammonia molecules have also been calculated for different temperatures. (author)

  1. Tritium in reprocessing plants: a study of the inventory, behavior, and the possibilities of separation of the tritium isotope

    International Nuclear Information System (INIS)

    Schnez, H.; Laser, M.; Merz, E.

    The path followed by tritium in reprocessing plants is described in quantitative terms based on the Purex and Thorex processes. Flowsheets are given for the Purex process which are on the one hand based on the present state of technology, but make provision at the same time for a recycling of the aqueous phase and a tritium separation. As an alternative approach the technical and economic aspects have been examined of a prior separation of the tritium after reduction of the fuel elements, followed by separation from the aqueous phase. The ultimate storage and transport of the separated tritium were included in the cost determination. The conclusion is reached as a result of the study that tritium separation is possible on scientific and technical grounds. The estimates made show the financial outlay to be less than 10 DM/GWh, but may on occasion be substantially higher, since no practical or industrial experience of the process is yet available

  2. Tritium Isotope Separation Using Adsorption-Distillation Column

    International Nuclear Information System (INIS)

    Fukada, Satoshi

    2005-01-01

    In order to miniaturize the height of a distillation tower for the detritiation of waste water from fusion reactors, two experiments were conducted: (1) liquid frontal chromatography of tritium water eluting through an adsorption column and (2) water distillation using a column packed with adsorbent particles. The height of the distillation tower depends on the height equivalent to a theoretical plate, HETP, and the equilibrium isotope separation factor, α H-T equi . The adsorption action improved not only HETP but also α H-T equi . Since the adsorption-distillation method proposed here can shorten the tower height with keeping advantages of the distillation, it may bring an excellent way for miniaturizing the distillation tower to detritiate a large amount of waste water from fusion reactors

  3. 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.)

  4. 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

  5. Tritium isotope separation from light and heavy water by bipolar electrolysis

    International Nuclear Information System (INIS)

    Petek, M.; Ramey, D.W.; Taylor, R.D.; Kobisk, E.H.

    1980-01-01

    A process for separating tritium from light and heavy water is described. Hydrogen is transferred at and through bipolar electrodes at rates H > D > T. In a cell containing several bipolar electrodes placed in series between two terminal electrodes, a flow of hydrogen is established from the terminal anode compartment toward the terminal cathode. An electrolyte feed containing tritium is continuously added to the system and is subsequently transported countercurrent to the hydrogen mass transfer. A cascaded system is established, in which effluent streams enriched and depleted in tritium can be withdrawn. The voltage drop is smaller at any bipolar electrode as compared to the voltage for normal electrolysis. Cell design is compact because isotope separation occurs at bipolar electrodes without evolution of gas. Isotope separation was demonstrated in laboratory cells where a steady-state tritium concentration gradient was attained. This gradient was in agreement with concentrations calculated from a derived mathematical model

  6. Laser separation of hydrogen isotopes: Tritium-from-deuterium recovery

    International Nuclear Information System (INIS)

    Magnotta, F.; Herman, I.P.; Aldridge, F.T.; Maienschein, J.L.

    1984-01-01

    Single-step enrichment factors exceeding 15,000 have been observed in the removal of tritium-from-deuterium by 12 μm laser multiple-photon dissociation of chloroform. The photochemistry and photophysics of this process is discussed along with prospects for implementation of this method in practical heavy water reactor detritiation. 7 refs., 7 figs., 1 tab

  7. Method of separating tritium contained in gaseous wastes

    International Nuclear Information System (INIS)

    Hashimoto, Yasuo; Oozono, Hideaki.

    1981-01-01

    Purpose: To decrease tritium concentration in gaseous wastes to less than the allowable level by removing tritium in gaseous wastes generated upon combustion of radioactive wastes by using a plurality of heat exchangers. Method: Gaseous wastes at high temperature generated upon combustion of radioactive wastes in an incinerator are removed with radioactive solid substances through filters, cooled down to a temperature below 10 0 C by the passage through first and second heat exchangers and decreased with tritium content to less than the allowable concentration by the gaseous wastes at low temperature from the second heat exhcanger. The gaseous wastes at low temperature are used as the cooling medium for the first heat exchanger. They are heat exchanged at the upstream of the second heat exchanger with the cooling water from the third heat exchanger and cooled at the downstream by the cooling water cooled by the cooling medium. The gaseous wastes at low temperature thus cooled below 10 0 C are heated to about 350 0 C in the first heat exchanger and discharged. (Moriyama, K.)

  8. Separation factor dependence upon cathode material for tritium separation from heavy water by electrolysis

    International Nuclear Information System (INIS)

    Ogata, Y.; Sakuma, Y.; Ohtani, N.; Kotaka, M.

    2002-01-01

    Using three cathode materials, i.e. carbon (C), stainless steel (SUS), and nickel (Ni), tritium was separated from heavy water by electrolysis, and the separation factors were compared. To separate hydrogen isotopes, heavy water was electrolyzed by an electrolysis device with a solid polymer electrode (SPE), which needed no electrolyte additives for electrolysis. The anode was made of 3 mm thickness of a sintered porous titanium plate covered with iridium oxide. The cathode was made of the same thickness of a sintered porous carbon, stainless steel, or nickel plate. Heavy water or light water spiked with tritiated water was electrolyzed 20 A x 60 min with the electrolysis cell temperature at 10, 20 or 30degC, and 15 A x 80 min at 5degC. The produced hydrogen and oxygen gases were recombined using a palladium catalyst with nitrogen gas as a carrier. The activities of the water in the electrolysis cell and of the recombined water were analyzed using a liquid scintillation counter. The apparent D-T separation factor (SF D/T ) and H-T separation factor (SF H/T ) were calculated as quotient the specific activity of the water in the cell divided by that of the recombined water. The electrolysis potential to keep the current 20 A was 2-3 V. The average yields of the recombined water were 95%. At the cell temperature of 20degC, SF D/T (C), SF D/T (SUS), and SF D/T (Ni) were 2.42, 2.17, and 2.05, respectively. At the same temperature, SF H/T (C), SF H/T (SUS), and SF H/T (Ni) were 12.5, 10.8, and 11.8, respectively. The SFs were in agreement with the results in other works. The SFs were changed with the cell temperature. (author)

  9. Tritium separation from heavy water by electrolysis with solid polymer electrolyte

    International Nuclear Information System (INIS)

    Ogata, Y.; Ohtani, N.; Kotaka, M.

    2003-01-01

    A tritium separation from heavy water by electrolysis using a solid polymer electrode layer was specified. The cathode was made of stainless steel or nickel. The electrolysis was performed for 1 hour at 5, 10, 20, and 30 deg C. Using a palladium catalyst, generated hydrogen and oxygen gases were recombined, which was collected with a cold trap. The activities of the samples were measured by a liquid scintillation counter. The apparent tritium separation factors of the heavy and light water at 20 deg C were ∼2 and ∼12, respectively. (author)

  10. Process for the separation of deuterium and tritium from water using ammonia and a hydrogen-nitrogen-mixture

    International Nuclear Information System (INIS)

    Mandrin, Ch.

    1986-01-01

    A multistage process for separation of deuterium and tritium from water using ammonia and a hydrogen-nitrogen mixture. In a first stage isotopic exchange takes place between water containing deuterium and tritium, and ammonia depleted in deuterium and tritium. The molar ammonia throughput is chosen to be greater than two third of the molar throughput of water. The advantage of the process consists in the fact that the main product is water almost entirely free from deuterium and tritium. The byproducts are compounds enriched in deuterium and tritium, and nitrogen enriched in N-15

  11. An assessment concerning the preparation and application of hydrocarbon catalysis for tritium separation

    International Nuclear Information System (INIS)

    Ionita, Gh.; Kitamoto, A.; Shimizu, M.

    2001-01-01

    Based on the long experience of the authors in the preparation, testing and evaluation of the performances of hydrophobic catalysts and on the reviewed references, this paper presents up-to-date R and D activities on the preparation and application of hydrophobic catalysts for tritium separation. Unlike the conventional hydrophilic catalysts, the hydrophobic catalysts repel the liquid water and allow the transport of the gaseous reactants and reaction products to and from catalytic active centers. For deuterium and tritium separation, over one hundred hydrophobic catalyst types have been prepared in different experimental conditions and tested by a large diversity of wet proofing methods. The influence on catalytic activity of about twenty parameters, have been also studied. The purpose of this paper is: (1) to provide a database for preparation and selection of he most appropriate catalyst and catalytic packing for the tritium separation; (2) to find how to use the hydrophobic catalyst and how to operate more efficiently the reactor packed with hydrophobic catalyst; (3) to evaluate the performances and potentiality of hydrophobic catalysts in tritium separation. As result, the following categories are shown: (1) the hydrophobic catalysts based on platinum and teflon as proved to have the highest activity and the longest stability by wet-proofing procedure; (2) the utilization of hydrophobic catalyst as ordered mixed catalytic packing in the trickle bed or separated bed reactors is more efficient and has been entirely tested on industrial scale; (3) the improvement of the inner geometry of the reactors and of the composition of mixed catalytic packing as well as the elaboration of the mathematical models for designing of the reactors and the evaluation of performances of separation processes constitute a major contribution of the authors; (4 ) a high resistance at radiation and chemical impurities of Pt-hydrophobic catalysts. The merits of hydrophobic Pt

  12. Applications of hydrophobic Pt catalysts in separation of tritium from liquid effluents

    International Nuclear Information System (INIS)

    Ionita, Gheorghe; Popescu, Irina; Stefanescu, Ioan; Varlam, Carmen

    2003-01-01

    Hydrophobic Pt catalysts were first prepared and used in deuterium or tritium separation while after their application was extended to chemical reactions occurring in liquid water or saturated humidity environments. Capillary condensing produced at the contact with liquid water or vapors engenders in classical hydrophilic catalysts a decrease in activity what makes them inefficient. Consequently, liquid water 'repealing' catalysts are to be used allowing, at the same time gaseous reactants and reaction products to diffuse to and fro the catalytic active centers. These catalysts were successfully applied in deuterium enrichment and tritium separation based on hydrogen- liquid water isotopic exchange at both pilot and industrial scale. High activity and a prolonged stability were demonstrated and checked in: - detritiation of the heavy water used as both moderator and coolant in CANDU type reactors; removing of tritium from light water recirculated in nuclear fuel reprocessing facilities; removal and recovery of tritium from atmosphere and tritium processing installations. Due to their incontestable advantages the use of these catalysts was recently extended to other chemical processes occurring in the presence of liquid water or in high humidity environment or else when water occurs as a reaction product, such as catalytic hydrogen - oxygen recombination at room temperature or removal of stable organic pollutants from waste waters

  13. Tritium enrichment of environmental waters by electrolysis: Development of cathodes exhibiting high isotopic separation and precise measurement of tritium enrichment factors

    International Nuclear Information System (INIS)

    Taylor, C.B.

    1976-01-01

    Equations are developed for the estimation of tritium enrichment in batch, continuous feed and periodic addition electrolysis cells. Optimum enrichment and minimum variability is obtained using developed cathode surfaces which catalyse the separation of tritium, as exhibited by the results of experiments using mild steel cathodes with NaOH electrolyte. The equations and various simple refinements of technique are applied to the determination of tritium enrichment factors by the spike cell method: for batch cells the standard errors are less than 1%. (author)

  14. Ligand exchange chromatography for analysis and preparative separation of tritium-labelled amino acids

    International Nuclear Information System (INIS)

    Zolotarev, Yu.A.; Zaitsev, D.A.; Penkina, V.I.; Dostavalov, I.N.; Myasoedov, N.F.

    1988-01-01

    Racemic tritium-labelled amino acids were separated into optical isomers by chromatography on a chiral polyacrylamide sorbent filled with copper ions. The polyacrylamide sorbent is synthesized by Mannich's reaction through the action of formaldehyde and L-phenylalanine upon polyacrylamide Biogel P-4 in an alkali phosphate buffer. Tritium-labelled amino acids are eluted by a weak alkali solution of ammonium carbonate. Data are presented on the ligand exchange chromatography of amino acids depending on the degree to which the sorbent is filled with copper ions and on the eluent concentration. Amino acids are isolated from the eluent on short columns filled with sulfonated cation exchanger in the H + form. HPLC on modified silica gel sorbents is also used for the analysis of tritium-labelled optically active amino acids. Amino acids are eluted by a weakly acidic water-methanol solution containing ammonium acetate. UV and scintillation flow type detectors are used. (author) 7 refs.; 8 figs

  15. Development of the ELEX process for tritium separation at reprocessing plants

    International Nuclear Information System (INIS)

    Bruggeman, A.; Meynendonckx, L.; Parmentier, C.; Goossens, W.R.A.; Baetsle, L.H.

    1985-01-01

    The ELEX process for isotopic enrichment and separation of tritium from aqueous reprocessing effluents is described. After the development of an appropriate hydrophobic catalyst and the study of the separate constituent steps of the ELEX process, an integrated bench-scale installation with a detritiation capacity of 10 mol water per hour was constructed. It comprises essentially a 1.5 kW electrolyser and two 2 cm diameter by 3 m high exchange columns. In this mini-pilot the ELEX process was successfully demonstrated by detritiating more than 1000 dm 3 water containing up to 100 mCi tritium per dm 3 , which is the feed concentration expected for application of the process in a reprocessing plant. The process decontamination factor was always larger than 100 and the overall tritium balance could be kept within the experimental errors of the various measurements. Depending on the duration of the runs, the volume reduction factor was between 10 and 15, but this factor will become much higher when the present electrolyser will be replaced by the low-volume one now under construction at S.C.K./C.E.N. The technical availability of the mini-pilot amounted to 99% or more for the last experiments. During the nearly 6000 hours of operation there were no tritium contamination problems. At present the construction of a 280 mol.h -1 or 0.12 m 3 H 2 O (HTO) per day pilot detritiation installation nears completion. In this unit, which will have a total tritium inventory of maximum 1000 Ci, the ELEX process will be demonstrated with a volume reduction factor of 100 and a process decontamination factor of 100. Again the feed concentration will be 100 Ci tritium per m 3 . In the future this installation will be supplemented with a pre-treatment unit for the removal of fission products, organics and nitric acid

  16. Separation and formation of ryanodine from dehydroryanodine. Preparation of tritium-labelled ryanodine

    International Nuclear Information System (INIS)

    Sutko, J.L.; Thompson, L.J.; Schlatterer, R.G.

    1986-01-01

    The commercially available preparation of the naturally occurring diterpene ester ryanodine contains several compounds in addition to ryanodine. These compounds were separated and purified using high performance liquid chromatography. The two major components, ryanodine and dehydroryanodine represented 90% of the material present. A method for the efficient reduction of dehydroryanodine to ryanodine was developed and used to produce ryanodine having tritium atoms at positions 19 and 20 and a specific activity of 60.8 Ci/mmole. (author)

  17. Tritium isotope separation by water distillation column packed with silica-gel beads

    International Nuclear Information System (INIS)

    Fukada, Satoshi

    2004-01-01

    Tritium enrichment or depletion by water distillation was investigated using a glass column of 32cm in height packed with silica-gel beads of 3.4mm in average diameter. The total separation factor of the silica-gel distillation column, α H-T , was compared with those of an open column distillation tower and of a column packed with stainless-steel Dixon rings. Depletion of the tritium activity in the distillate was enhanced by isotopic exchange with water absorbed on silica-gel beads that have a higher affinity for HTO than for H 2 O. The value of α H-T -1 of the silica-gel distillation column was about four times larger than that of a column without any packing and about two times larger than that of the Dixon-ring column. The improvement of α H-T by the silica-gel adsorbent indicated that the height of the distillation-adsorption column becomes shorter than that of the height of conventional distillation columns. (author)

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

    Energy Technology Data Exchange (ETDEWEB)

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

    1962-01-15

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

  19. Setup and commissioning of a combined water detritiation and isotope separation experiment at the Tritium Laboratory Karlsruhe

    Energy Technology Data Exchange (ETDEWEB)

    Welte, S., E-mail: stefan.welte@kit.edu; Cristescu, I.; Dittrich, H.; Lohr, N.; Melzer, C.; Michling, R.; Plusczyk, C.; Schaefer, P.

    2013-10-15

    Highlights: • Technical scale, tritium compatible liquid phase catalytic exchange (LPCE). • Technical scale, tritium compatible cryogenic distillation. • Combines processing option for tritiated water and isotope separation. -- Abstract: The European union in kind supply for the ITER fuel cycle development consists, among others, of the water detritiation system (WDS) and the isotope separation system (ISS). In order to mitigate the release of tritium to the environment, these systems are combined by feeding hydrogen exhaust from the ISS into the WDS for final processing. Therefore, the WDS is the final tritium barrier before releasing hydrogen (H{sub 2}) exhaust to the environment. The TRENTA 4 scaled prototype facility at TLK is based on combination of the combined electrolysis and catalytic exchange (CECE) process and a cryogenic distillation (CD) process. All components are fully tritium compatible and controlled using a state of the art control system for process automation, backed up by an additional dedicated safety system. The paper will give a detailed overview of the current experimental facility including all process components. Furthermore the paper will present the results of the functional test of the WDS/ISS combination using protium and deuterium, as well the results of the first commissioning runs using HTO of approximately 5 × 10{sup 9} Bq kg{sup −1} activity concentration.

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

    International Nuclear Information System (INIS)

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

    1975-01-01

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

  1. Characteristics improvement of hydrophobic polytetrafluoroethylene-platinum catalysts for tritium separation

    International Nuclear Information System (INIS)

    Popescu, I.; Ionita, Gh.; Dobrinescu, D.; Varlam, C.; Stefanescu, I.

    2006-01-01

    Full text: Based on the long experience of the authors in the preparation, testing and evaluation of the performances of hydrophobic catalysts and based on the reviewed references, this paper presents up-to-date R and D activities on the preparation methods and applications of the hydrophobic catalysts in tritium separation. The objectives of the paper are: how to improve the characteristics and performance of platinum hydrophobic catalysts; to assess and find a new procedure for the preparation of a new improved hydrophobic catalyst. From reviewed references one can conclude that platinum is the most active and efficient catalytic metal while the polytetrafluoroethylene is the best wet-proofing agent. A new improved hydrophobic Pt-catalyst has been proposed and its testing is now underway. The main steps and experimental conditions of preparation are thoroughly discussed. A new wet-proofing agent and new binders (titanium dioxide, cerium dioxide, zirconium dioxide) with a catalytic role are proposed and tested. The physico-structural parameters of the improved catalyst have been determined and are discussed in detail. The new proposal is a promising idea to improve the performance of conventional hydrophobic Pt-catalysts. (authors)

  2. Treatment and separation of radioactive fission products tritium, rare gases and iodine in nuclear fuel reprocessing plants

    Energy Technology Data Exchange (ETDEWEB)

    Schnez, H.

    1975-07-15

    Rare gases must be separated from the process off-gases of the head-end of the Purex and Thorex processes. To achieve high decontamination factors, the quantity of off-gas should be kept as low as possible. For rare gas separation, there are two possible methods of routing the off-gas: (a) the open flushing gas circuit, in which the purified off-gas (generally air) is passed off via the stack and (b) the closed circuit in which the off-gas (nitrogen or rare gases) is recycled to the dissolver after purification. Tritium must not be entrained into the second extraction cycle or be emitted with off-gases in the form of water vapor (HTO) or HT, but must remain completely in the aqueous phase. Most of the process water is recycled, as a result of which the tritium becomes concentrated in it. This tritiated water is then subjected to tritium rectification at a suitable point in the process. Iodine is very difficult to isolate to a small number of process stages. Present aim is to release the iodine in the dissolver stage into the off-gas, so as to prevent it being entrained into the extraction part. By the injection of hot nitrogen or water vapor into the dissolver or into iodine-containing condensates, all of the iodine is passed into the gaseous phase. Scrubbers can also be used together with iodine-containing condensates to adjust the scrubbing solution. Capital cost of separation plants account for 1 to 10 percent of the total cost of the reprocessing installation, and even more if a sophisticated tritium separation system is required. (DLC)

  3. Control, monitoring and data acquisition systems in pilot plant for tritium and deuterium separation

    International Nuclear Information System (INIS)

    Retevoi, Carmen; Balteanu, Ovidiu Ioan

    1999-01-01

    To achieve the control, monitoring and data acquisition for a pilot plant for tritium and deuterium separation we have developed a system based on computer processing which transfers and treats all the data from the physical system. It consists of six basic elements: 1. a process computer ; 2. a National Instruments Amplifier/Multiplexed - SCXI 1000 with a SCXI 1100 Module with 32 differential input channels; 3. a Honeywell Digital Process Recorder - DPR 250, with 32 universal input, 12 digital input and 12 internal relays; 4. a control system for 4 throttle valves; 5. a National Instruments Data Acquisition board - AT-MIO-16XE-10, with 8 differential channels; 6. a system consisting of up to 20 digital programming current units for carbon RTD's. All the parameters from transducers, sensors and transmitters are introduced into the multiplexer and beyond into the acquisition data board. With LabVIEW soft support (National Instrument product), we made a graphic interface which displays the plant and all the parameters and their points of measure and cumulates all these data into a file. On the other hand all the pressure flow and level values are monitored by the recorder DPR 250, which has a RS232/RS485 port for PC communication. The temperatures are measured with carbon RTD's and a system comprising 20 programming current units connected by RS485 serial bus and a RS485/RS232 converter directly to the serial port of process computer. A special program makes the voltage/temperature conversion. The control system for throttle valves comprises a central unit, which communicates by RS232 bus with 4 controllers commanding 4 stepping motors. Every stepping motor is linked by a reductor to the throttle valve. This system can operate in either manual or automatic mode. The central unit can communicate with process computer via RS232 link. In this way a process computer can receive all the parameters by means of RS232/RS245 link or directly through the multiplexer and

  4. New concepts for the recovery and isotopic separation of tritium in fusion reactors

    International Nuclear Information System (INIS)

    Dombra, A.H.; Holtslander, W.J.; Miller, A.I.; Canadian Fusion Fuels Technology Project, Toronto, Ontario)

    1986-01-01

    New concepts for the recovery of tritium from light water coolant of LiPb blankets, and high-pressure helium coolant of Li-ceramic blankets are introduced. Application of these concepts to fusion reactors is illustrated with conceptual system designs for the anticipated NET blanket requirements. (author)

  5. Novel Methods of Tritium Sequestration: High Temperature Gettering and Separation Membrane Materials Discovery for Nuclear Energy Systems

    Energy Technology Data Exchange (ETDEWEB)

    Chen, Franglin [Univ. of South Carolina, Columbia, SC (United States); Sholl, David [Georgia Inst. of Technology, Atlanta, GA (United States); Brinkman, Kyle [Savannah River Site (SRS), Aiken, SC (United States). Savannah River National Lab. (SRNL); Lyer, Ratnasabapathy [Claflin Univ., Orangeburg, SC (United States); Iyer, Ratnasabapathy [Claflin Univ., Orangeburg, SC (United States); Reifsnider, Kenneth [Univ. of South Carolina, Columbia, SC (United States)

    2015-01-22

    This project is aimed at addressing critical issues related to tritium sequestration in next generation nuclear energy systems. A technical hurdle to the use of high temperature heat from the exhaust produced in the next generation nuclear processes in commercial applications such as nuclear hydrogen production is the trace level of tritium present in the exhaust gas streams. This presents a significant challenge since the removal of tritium from the high temperature gas stream must be accomplished at elevated temperatures in order to subsequently make use of this heat in downstream processing. One aspect of the current project is to extend the techniques and knowledge base for metal hydride materials being developed for the ''hydrogen economy'' based on low temperature absorption/desorption of hydrogen to develop materials with adequate thermal stability and an affinity for hydrogen at elevated temperatures. The second focus area of this project is to evaluate high temperature proton conducting materials as hydrogen isotope separation membranes. Both computational and experimental approaches will be applied to enhance the knowledge base of hydrogen interactions with metal and metal oxide materials. The common theme between both branches of research is the emphasis on both composition and microstructure influence on the performance of sequestration materials.

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

    International Nuclear Information System (INIS)

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

    1995-01-01

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

  7. Novel Methods of Tritium Sequestration: High Temperature Gettering and Separation Membrane Materials Discovery for Nuclear Energy Systems

    International Nuclear Information System (INIS)

    2015-01-01

    This project is aimed at addressing critical issues related to tritium sequestration in next generation nuclear energy systems. A technical hurdle to the use of high temperature heat from the exhaust produced in the next generation nuclear processes in commercial applications such as nuclear hydrogen production is the trace level of tritium present in the exhaust gas streams. This presents a significant challenge since the removal of tritium from the high temperature gas stream must be accomplished at elevated temperatures in order to subsequently make use of this heat in downstream processing. One aspect of the current project is to extend the techniques and knowledge base for metal hydride materials being developed for the ''hydrogen economy'' based on low temperature absorption/desorption of hydrogen to develop materials with adequate thermal stability and an affinity for hydrogen at elevated temperatures. The second focus area of this project is to evaluate high temperature proton conducting materials as hydrogen isotope separation membranes. Both computational and experimental approaches will be applied to enhance the knowledge base of hydrogen interactions with metal and metal oxide materials. The common theme between both branches of research is the emphasis on both composition and microstructure influence on the performance of sequestration materials.

  8. 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

  9. Role of the chemical engineering technician in applied research related to tritium separation from aqueous effluents

    International Nuclear Information System (INIS)

    Nelson, S.D.

    1978-01-01

    Applied research and development activities related to the removal of tritium from aqueous effluent streams have presented broad opportunities to the chemical engineering technician for professional growth. Technician job activities involve operating complex analytical instrumentation and constructing, maintaining, and operating experimental electrolysis apparatus. The technician is a member of a professional team including scientific, engineering, and other technical personnel and as such is expected to exercise creative thought. Proximity of a large university and availability of formalized ''in house'' training courses provide incentives for technicians to broaden their academic base concurrent with their work involvement

  10. Analysis of the separation of protium from blanket tritium-product streams

    International Nuclear Information System (INIS)

    Misra, B.; Maroni, V.A.

    1981-07-01

    The case is considered in which the blanket product stream has been purified to the point where only protium, tritium, and a small quantity of deuterium remain. A cryogenic distillation cascade concept developed specifically to handle this enrichment problem is shown. The concept is based on a series of distillation columns and equilibrators capable of producing a protium-rich stream containing less than 1000 appm T and a tritium-rich stream containing less than 2000 appm H. It is envisioned that both of these streams could be blended with streams of comparable composition in the mainstream position of the fuel cycle without further processing. The computational analysis of the cascade was based on a fixed arrangement of columns and equilibrators and a fixed number of theoretical plates per columns, since these features are less easily varied in an actual system than reflux ratios and flow rates. In order to test the flexibility of this conceptual enruchment system to adjust to variations of the H/T ratio in the feed, H/T values of 0.333, 1.00, and 3.00 were investigated

  11. 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.)

  12. 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

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

    International Nuclear Information System (INIS)

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

    2003-01-01

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

  14. Radiochemical Separation and Quantification of Tritium in Metallic Radwastes Generated from CANDU Type NPP - 13279

    Energy Technology Data Exchange (ETDEWEB)

    Ahn, H.J.; Choi, K.C.; Choi, K.S.; Park, T.H.; Park, Y.J.; Song, K. [Korea Atomic Energy Research Institute, P.O. Box 105, Yuseong, Daejeon, 305-330 (Korea, Republic of)

    2013-07-01

    As a destructive quantification method of {sup 3}H in low and intermediate level radwastes, bomb oxidation, sample oxidation, and wet oxidation methods have been introduced. These methods have some merits and demerits in the radiochemical separation of {sup 3}H radionuclides. That is, since the bomb oxidation and sample oxidation methods are techniques using heating at high temperature, the separation methods of the radionuclides are relatively simple. However, since {sup 3}H radionuclide has a property of being diffused deeply into the inside of metals, {sup 3}H which is distributed on the surface of the metals can only be extracted if the methods are applied. As an another separation method, the wet oxidation method makes {sup 3}H oxidized with an acidic solution, and extracted completely to an oxidized HTO compound. However, incomplete oxidized {sup 3}H compounds, which are produced by reactions of acidic solutions and metallic radwastes, can be released into the air. Thus, in this study, a wet oxidation method to extract and quantify the {sup 3}H radionuclide from metallic radwastes was established. In particular, a complete extraction method and complete oxidation method of incomplete chemical compounds of {sup 3}H using a Pt catalyst were studied. The radioactivity of {sup 3}H in metallic radwastes is extracted and measured using a wet oxidation method and liquid scintillation counter. Considering the surface dose rate of the sample, the appropriate size of the sample was determined and weighed, and a mixture of oxidants was added to a 200 ml round flask with 3 tubes. The flask was quickly connected to the distilling apparatus. 20 mL of 16 wt% H{sub 2}SO{sub 4} was given into the 200-ml round flask through a dropping funnel while under stirring and refluxing. After dropping, the temperature of the mixture was raised to 96 deg. C and the sample was leached and oxidized by refluxing for 3 hours. At that time, the incomplete oxidized {sup 3}H compounds were

  15. 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)

  16. 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

  17. 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

  18. Tritium monitor with improved gamma-ray discrimination

    Science.gov (United States)

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

    1985-01-01

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

  19. 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.)

  20. Tritium breeding blanket

    International Nuclear Information System (INIS)

    Smith, D.; Billone, M.; Gohar, Y.; Baker, C.; Mori, S.; Kuroda, T.; Maki, K.; Takatsu, H.; Yoshida, H.; Raffray, A.; Sviatoslavsky, I.; Simbolotti, G.; Shatalov, G.

    1991-01-01

    The terms of reference for ITER provide for incorporation of a tritium breeding blanket with a breeding ratio as close to unity as practical. A breeding blanket is required to assure an adequate supply of tritium to meet the program objectives. Based on specified design criteria, a ceramic breeder concept with water coolant and an austenitic steel structure has been selected as the first option and lithium-lead blanket concept has been chosen as an alternate option. The first wall, blanket, and shield are integrated into a single unit with separate cooling systems. The design makes extensive use of beryllium to enhance the tritium breeding ratio. The design goals with a tritium breeding ratio of 0.8--0.9 have been achieved and the R ampersand D requirements to qualify the design have been identified. 4 refs., 8 figs., 2 tabs

  1. 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)

  2. 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

  3. 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.

  4. 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.

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

    International Nuclear Information System (INIS)

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

    2010-01-01

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

  6. 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

  7. 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

  8. Tritium in the food chain

    International Nuclear Information System (INIS)

    Koenig, L.A.

    1988-01-01

    Tritium is a hydrogen isotope taking part in the global hydrogen cycle as well as in all metabolic processes. The resultant problems with respect to the food chain are summarized briefly with emphasis on 'organically bound tritium'. However, only a small number of the numerous publications on this topic can be taken into consideration. Publications describing experiments under defined conditions are reported, thus allowing a semiempirical interpretation to be made. Tritium activity measurements of food grown in the vicinity of the Karlsruhe Nuclear Research Center have been carried out. A list of the results is given. A dose assessment is performed under simplifying assumptions. Even when the organically bound tritium is taken into account, a radiation exposure of less than 1% of that of K-40 is obtained under these conditions. To avoid misinterpretation, the specific activity (Bq H-3/g H) of water-bound and organically bound tritium has to be considered separately. (orig.) [de

  9. Tritium immobilisation

    International Nuclear Information System (INIS)

    Bridger, N.J.

    1982-01-01

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

  10. 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)

  11. 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)

  12. Tritium Systems Test Facility. Volume II. Appendixes

    International Nuclear Information System (INIS)

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

    1976-10-01

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

  13. History of 232-F, tritium extraction processing

    International Nuclear Information System (INIS)

    Blackburn, G.W.

    1994-08-01

    In 1950 the Atomic Energy Commission authorized the Savannah River Project principally for the production of tritium and plutonium-239 for use in thermonuclear weapons. 232-F was built as an interim facility in 1953--1954, at a cost of $3.9M. Tritium extraction operations began in October, 1955, after the reactor and separations startups. In July, 1957 a larger tritium facility began operation in 232-H. In 1958 the capacity of 232-H was doubled. Also, in 1957 a new task was assigned to Savannah River, the loading of tritium into reservoirs that would be actual components of thermonuclear weapons. This report describes the history of 232-F, the process for tritium extraction, and the lessons learned over the years that were eventually incorporated into the new Replacement Tritium Facility

  14. Desactivation of tritium waters by rectification methods

    International Nuclear Information System (INIS)

    Egorov, A.I.; Tyunis, V.M.

    2002-01-01

    Results of experiments into the basic rectification processes dedicated to tritium separation from reactor, technological and waste waters are presented. Coefficients of separation for rectification of water (1.028), ammonia (1.05), azeotrope H 2 O - HTO - HNO 3 (1.098) and D 2 O - DTO - DNO 3 (1.039) are performed. Operating schemes of tritium separating units are reviewed [ru

  15. 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)

  16. 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)

  17. Technology and component development for a closed tritium cycle

    International Nuclear Information System (INIS)

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

    1991-01-01

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

  18. Magmatic tritium

    International Nuclear Information System (INIS)

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

    1997-01-01

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

  19. 1997 evaluation of tritium removal and mitigation technologies for Hanford Site wastewaters

    International Nuclear Information System (INIS)

    Jeppson, D.W.; Biyani, R.K.; Duncan, J.B.; Flyckt, D.L.; Mohondro, P.C.; Sinton, G.L.

    1997-01-01

    This report contains results of a biennial assessment of tritium separation technology and tritium nitration techniques for control of tritium bearing wastewaters at the Hanford Site. Tritium in wastewaters at Hanford have resulted from plutonium production, fuel reprocessing, and waste handling operations since 1944. this assessment was conducted in response to the Hanford Federal Facility Agreement and Consent Order

  20. Tritium proof-of-principle pellet injector

    International Nuclear Information System (INIS)

    Fisher, P.W.

    1991-07-01

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

  1. 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

  2. Tritium accountancy

    International Nuclear Information System (INIS)

    Avenhaus, R.; Spannagel, G.

    1995-01-01

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

  3. 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

  4. Development of tritium-handling technique

    International Nuclear Information System (INIS)

    Ohmura, Hiroshi; Hosaka, Akio; Okamoto, Takahumi

    1988-01-01

    The overview of developing activities for tritium-handling techniques in IHI are presented. To establish a fusion power plant, tritium handling is one of the key technologies. Recently in JAERI, conceptual design of FER (Fusion Experimental Reactor) has been carried out, and the FER system requires a processing system for a large amount of tritium. IHI concentrate on investigation of fuel gas purification, isotope separation and storage systems under contract with Toshiba Corporation. Design results of the systems and each components are reviewed. IHI has been developing fundamental handling techniques which are the ZrNi bed for hydrogen isotope storage and isotope separation by laser. The ZrNi bed with a tritium storage capacity of 1000 Ci has been constructed and recovery capability of the hydrogen isotope until 10 -4 Torr {0.013 Pa} was confirmed. In laser isotope separation, the optimum laser wave length has been determined. (author)

  5. Methane generated from graphite--tritium interaction

    International Nuclear Information System (INIS)

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

    1979-01-01

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

  6. Handling of tritium-bearing wastes

    International Nuclear Information System (INIS)

    1981-01-01

    The generation of nuclear power and reprocessing of nuclear fuel results in the production of tritium and the possible need to control the release of tritium-contaminated effluents. In assessing the need for controls, it is necessary to know the production rates of tritium at different nuclear facilities, the technologies available for separating tritium from different gaseous and liquid streams, and the methods that are satisfactory for storage and disposal of tritiated wastes. The intention in applying such control technologies and methods is to avoid undesirable effects on the environment, and to reduce the radiation burden on operational personnel and the general population. This technical report is a result of the IAEA Technical Committee Meeting on Handling of Tritium-bearing Effluents and Wastes, which was held in Vienna, 4 - 8 December 1978. It summarizes the main topics discussed at the meeting and appends the more detailed reports on particular aspects that were prepared for the meeting by individual participants

  7. Extraction of tritium from liquid lithium by permeation

    International Nuclear Information System (INIS)

    Alire, R.M.

    1978-01-01

    This paper assesses a method for extracting tritium from liquid lithium for specific application to the conceptual laser fusion reactor that uses a continuous lithium ''waterfall.'' The tritium diffuses through a refractory metal that contains a getter and is then stored in a hydride-forming alloy. There are various uncertainties with this method including helium-4 extraction, unknown impurities that may accumulate in liquid lithium, the effects of these impurities on tritium separation, and the maintenance of tritium-contaminated equipment. Our study indicates that major tritium losses will occur during equipment maintenance rather than as a result of permeation losses through the primary vessel

  8. Conceptual design of tritium treatment facility

    International Nuclear Information System (INIS)

    Tachikawa, Katsuhiro

    1982-01-01

    In connection with the development of fusion reactors, the development of techniques concerning tritium fuel cycle, such as the refining and circulation of fuel, the recovery of tritium from blanket, waste treatment and safe handling, is necessary. In Japan Atomic Energy Research Institute, the design of the tritium process research laboratory has been performed since fiscal 1977, in which the following research is carried out: 1) development of hydrogen isotope separation techniques by deep cooling distillation method and thermal diffusion method, 2) development of the refining, collection and storage techniques for tritium using metallic getters and palladium-silver alloy films, and 3) development of the safe handling techniques for tritium. The design features of this facility are explained, and the design standard for radiation protection is shown. At present, in the detailed design stage, the containment of tritium and safety analysis are studied. The building is of reinforced concrete, and the size is 48 m x 26 m. Glove boxes and various tritium-removing facilities are installed in two operation rooms. Multiple wall containment system and tritium-removing facilities are explained. (Kako, I.)

  9. Tritium Systems Test Facility. Volume I

    International Nuclear Information System (INIS)

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

    1976-10-01

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

  10. 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)

  11. Method of extracting tritium from heavy water

    International Nuclear Information System (INIS)

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

    1979-01-01

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

  12. Tritium removal using vanadium hydride

    International Nuclear Information System (INIS)

    Hill, F.B.; Wong, Y.W.; Chan, Y.N.

    1978-01-01

    The results of an initial examination of the feasibility of separation of tritium from gaseous protium-tritium mixtures using vanadium hydride in cyclic processes is reported. Interest was drawn to the vanadium-hydrogen system because of the so-called inverse isotope effect exhibited by this system. Thus the tritide is more stable than the protide, a fact which makes the system attractive for removal of tritium from a mixture in which the light isotope predominates. The initial results of three phases of the research program are reported, dealing with studies of the equilibrium and kinetics properties of isotope exchange, development of an equilibrium theory of isotope separation via heatless adsorption, and experiments on the performance of a single heatless adsorption stage. In the equilibrium and kinetics studies, measurements were made of pressure-composition isotherms, the HT--H 2 separation factors and rates of HT--H 2 exchange. This information was used to evaluate constants in the theory and to understand the performance of the heatless adsorption experiments. A recently developed equilibrium theory of heatless adsorption was applied to the HT--H 2 separation using vanadium hydride. Using the theory it was predicted that no separation would occur by pressure cycling wholly within the β phase but that separation would occur by cycling between the β and γ phases and using high purge-to-feed ratios. Heatless adsorption experiments conducted within the β phase led to inverse separations rather than no separation. A kinetic isotope effect may be responsible. Cycling between the β and γ phases led to separation but not to the predicted complete removal of HT from the product stream, possibly because of finite rates of exchange. Further experimental and theoretical work is suggested which may ultimately make possible assessment of the feasibility and practicability of hydrogen isotope separation by this approach

  13. 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

  14. Technologies for immobilization and disposal of tritium

    International Nuclear Information System (INIS)

    Coppari, N.R.

    1996-01-01

    This study was done within a program one of whose objectives was to know the state of the technology development for tritium separation in the moderator circuit at HWR and to define the possible technologies to be applied to the Argentine nuclear power plants. Within this framework the strategies adopted by each country and the available technologies for a safe disposal of tritium, not only in its gaseous state tritium but also as tritiated water were analyzed. It is considered that if the selected separation method is such that the tritium is in its gaseous state, the hydride formation for long periods of immobilization should be studied. whereas if it were triated water immobilization should be studied to choose the technology between cementation and drying agents, in both cases the final disposal site will have to be selected. (author). 8 refs

  15. The Tritium White Paper

    International Nuclear Information System (INIS)

    2009-01-01

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

  16. Tritium-surface interactions

    International Nuclear Information System (INIS)

    Kirkaldy, J.S.

    1983-06-01

    The report deals broadly with tritium-surface interactions as they relate to a fusion power reactor enterprise, viz., the vacuum chamber, first wall, peripherals, pumping, fuel recycling, isotope separation, repair and maintenance, decontamination and safety. The main emphasis is on plasma-surface interactions and the selection of materials for fusion chamber duty. A comprehensive review of the international (particularly U.S.) research and development is presented based upon a literature review (about 1 000 reports and papers) and upon visits to key laboratories, Sandia, Albuquerque, Sandia, Livermore and EGβG Idaho. An inventory of Canadian expertise and facilities for RβD on tritium-surface interactions is also presented. A number of proposals are made for the direction of an optimal Canadian RβD program, emphasizing the importance of building on strength in both the technological and fundamental areas. A compendium of specific projects and project areas is presented dealing primarily with plasma-wall interactions and permeation, anti-permeation materials and surfaces and health, safety and environmental considerations. Potential areas of industrial spinoff are identified

  17. 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%

  18. 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

  19. 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

  20. [Mechanism of tritium persistence in porous media like clay minerals].

    Science.gov (United States)

    Wu, Dong-Jie; Wang, Jin-Sheng; Teng, Yan-Guo; Zhang, Ke-Ni

    2011-03-01

    To investigate the mechanisms of tritium persistence in clay minerals, three types of clay soils (montmorillonite, kaolinite and illite) and tritiated water were used in this study to conduct the tritium sorption tests and the other related tests. Firstly, the ingredients, metal elements and heat properties of clay minerals were studied with some instrumental analysis methods, such as ICP and TG. Secondly, with a specially designed fractionation and condensation experiment, the adsorbed water, the interlayer water and the structural water in the clay minerals separated from the tritium sorption tests were fractionated for investigating the tritium distributions in the different types of adsorptive waters. Thirdly, the location and configuration of tritium adsorbed into the structure of clay minerals were studied with infrared spectrometry (IR) tests. And finally, the forces and mechanisms for driving tritium into the clay minerals were analyzed on the basis of the isotope effect of tritium and the above tests. Following conclusions have been reached: (1) The main reason for tritium persistence in clay minerals is the entrance of tritium into the adsorbed water, the interlayer water and the structural water in clay minerals. The percentage of tritium distributed in these three types of adsorptive water are in the range of 13.65% - 38.71%, 0.32% - 5.96%, 1.28% - 4.37% of the total tritium used in the corresponding test, respectively. The percentages are different for different types of clay minerals. (2) Tritium adsorbed onto clay minerals are existed in the forms of the tritiated hydroxyl radical (OT) and the tritiated water molecule (HTO). Tritium mainly exists in tritiated water molecule for adsorbed water and interlayer water, and in tritiated hydroxyl radical for structural water. (3) The forces and effects driving tritium into the clay minerals may include molecular dispersion, electric charge sorption, isotope exchange and tritium isotope effect.

  1. 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.)

  2. 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

  3. Generation of gaseous tritium standards

    International Nuclear Information System (INIS)

    Hohorst, F.A.

    1994-09-01

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

  4. ITER Dynamic Tritium Inventory Modeling Code

    International Nuclear Information System (INIS)

    Cristescu, Ioana-R.; Doerr, L.; Busigin, A.; Murdoch, D.

    2005-01-01

    A tool for tritium inventory evaluation within each sub-system of the Fuel Cycle of ITER is vital, 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 modeling its hold-up within each sub-system and by validating these models in real-time against the monitored flows and tritium streams between the systems. To get reliable results, an accurate dynamic modeling of the tritium content in each sub-system is necessary. In order to optimize the configuration and operation of the ITER fuel cycle, a dynamic fuel cycle model was developed progressively in the decade up to 2000-2001. As the design for some sub-systems from the fuel cycle (i.e. Vacuum pumping, Neutral Beam Injectors (NBI)) have substantially progressed meanwhile, a new code developed under a different platform to incorporate these modifications has been developed. The new code is taking over the models and algorithms for some subsystems, such as Isotope Separation System (ISS); where simplified models have been previously considered, more detailed have been introduced, as for the Water Detritiation System (WDS). To reflect all these changes, the new code developed inside EU participating team was nominated TRIMO (Tritium Inventory Modeling), to emphasize the use of the code on assessing the tritium inventory within ITER

  5. 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)

  6. Investigation of tritium incorporation by means of excreted metabolites

    International Nuclear Information System (INIS)

    Biro, T.; Szilagyi, M.

    1978-01-01

    The commonly accepted urine analysis by liquid scintillation method was applied for whole body dose estimating. After the separation of metabolite fractions the organically bound tritium in urine could be measured. Urine samples from workers repeatedly exposed to tritium incorporation during the chemical processing of various labeled compounds have been collected and analyzed. The time dependence of tritium activity in certain metabolites was found to be characteristic, significantly differing from the 3 H concentration curve of the native or treated urine sample. (Auth.)

  7. Tritium proof-of-principle injector experiment

    International Nuclear Information System (INIS)

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

    1988-01-01

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

  8. 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

  9. 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

  10. 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.

  11. 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

  12. 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

  13. Technology and component development for a closed tritium cycle

    International Nuclear Information System (INIS)

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

    1991-01-01

    A brief summary on recent advances in the field of tritium technology concerning the most important subsystems of the fuel cycle of a fusion reactor, i.e. the plasma exhaust pumping system, the exhaust gas clean up system, the isotope separation, the tritium storage and the tritium extraction from a blanket is provided. Experimental results, single component developments, and technical tests including those with relevant amounts of tritium that constitute the basis of proposed integral process concepts are described. 48 refs., 2 tabs

  14. Analysis and speciation of the tritium in environmental matrices

    International Nuclear Information System (INIS)

    Bacchetta, Audrey

    2014-01-01

    This study deals with environmental monitoring. The main aims are (i) the optimisation of the analytical procedure for the tritium in organic form determination, and (ii) the identification of the tritium bearing molecules which are responsible for its transfer from the environment to man. The study was divided into three stages. First an analytical method was developed to determine hydrogen content of several samples, which is a key element to calculate accurate organically bound tritium activities. Secondly, the impact of the organically bound tritium fractions separation (labile exchange) for the determination of the representative fraction of the level of environmental tritium activity was then evaluated. For that, the amount of solubilised sample was estimated. Finally, the speciation of tritium in environmental samples was investigated. Several molecules classes and organic compounds dissolved in the labile exchanges solvent were identified. The results show that the distribution of tritium in organisms depends on both properties of the chemical bond in which it is involved and chemical properties of tritium bearing molecules. The identified compounds belong to the molecules classes such as carbohydrates or amino acids, constitutive of living organisms. It would now be of interest to study the tritium distribution in an environmental sample to target molecules of interest and study the impact of tritium from the environment to man. (author) [fr

  15. 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.)

  16. Tritium sources; Izvori tricijuma

    Energy Technology Data Exchange (ETDEWEB)

    Glodic, S [Institute of Nuclear Sciences VINCA, Belgrade (Yugoslavia); Boreli, F [Elektrotehnicki fakultet, Belgrade (Yugoslavia)

    1993-07-01

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

  17. 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

  18. AKUT: a process for the separation of aerosols, krypton, and tritium from burner off-gas in HTR-fuel reprocessing

    International Nuclear Information System (INIS)

    Laser, M.; Barnert-Wiemer, H.; Beaujean, H.; Merz, E.; Vygen, H.

    1975-01-01

    The AKUT process consists of the following process steps: (1) aerosol retention by an electrostatic separator followed by HEPA filters, (2) oxidation of CO with O 2 or reaction of excess O 2 with CO, respectively, (3) compression, (4) scrubbing and/or liquefaction, (5) separation of krypton by distillation, and (6) separation of tritiated water and iodine by adsorption or chemical reaction. Liquefied off-gas with low permanent gas content resulting from graphite burning with oxygen may be distilled at ambient temperature. Off-gas with higher permanent gas content from burning with oxygen enriched air must be processed at lower temperature. The ambient temperature flow sheet is preferable from an economic as well as safety point of view. (U.S.)

  19. Distillation plant for tritium enrichment in metallic lithium

    International Nuclear Information System (INIS)

    Barnert, E.; Butzek, D.; Cordewiner, J.; Heinrichs, E.

    1984-06-01

    To close the external fuel cycle of fusion reactors, the tritium obtained from lithium must be separated off. One way of doing this is by high-temperature distillation and subsequent permeation. The construction of high-temperature distillation plant is described. For the time being, deuterium is processed instead of tritium. (orig.) [de

  20. Tritium ingestion as organically bound tritium (OBT) - incorporation in different organs of pregnant and non-pregnant rats

    International Nuclear Information System (INIS)

    Bhatia, A.L.; Pollaris, K.; Vandecasteele, C.M.; Kowalska, M.

    1998-01-01

    For a better understanding of the hazard of tritium, its bound form in the food constituents (organically bound tritium (OBT)) has not been investigated though study on tritiated water are many. Hence an evaluation of the uptake of tritium incorporated in basic constituents of food viz, proteins, carbohydrates and lipids is warranted. Present study cells with the incorporated three organically bound tritium components separated from tritiated milk powder (casein, butter and lactose). This is further compared in the organs of pregnant (after parturition) and non-pregnant rats

  1. A metabolic derivation of tritium transfer factors in animal products

    International Nuclear Information System (INIS)

    Galeriu, D.; Melintescu, A.; Crout, N. M. J.; Bersford, N. A.; Peterson, S. R.; Hess, M. van

    2001-01-01

    Tritium is a potentially important environmental contaminant arising from the nuclear industry. Because tritium is an isotope of hydrogen, its behaviour in the environment is controlled by the behaviour of hydrogen. Chronic releases of tritium to the atmosphere, in particular, will result in tritium-to-hydrogen (T/H) ratios in plants and animals that are more or less in equilibrium with T/H ratios in the air moisture. Tritium is thus a potentially important contaminant of plant and animal food products. The transfer of tritium from air moisture to plants is quite well understood. In contrast, although a number of regulatory agencies have published transfer coefficient values for diet tritium transfer for a limited number of animal products, a fresh evaluation of these transfers needs to be made In this paper we present an approach for the derivation of tritium transfer coefficients which is based on the metabolism of hydrogen in animals in conjunction with experimental data on tritium transfer. The derived transfer coefficients separately account for transfer to and from free (i.e. water) and organically bound tritium. The predicted transfer coefficients are compared to available data independent of model development. Agreement is good, with the exception of the transfer coefficient for transfer from tritiated water to organically bound tritium in ruminants, which may be attributable to the particular characteristics of ruminant digestion. We show that transfer coefficients will vary in response to the metabolic status of an animal (e.g. stage of lactation, digestibility of diet, etc.) and that the use of a single transfer coefficient from diet to animal product is not appropriate for tritium. It is possible to derive concentration ratio values which relate the concentration of tritiated water and organically bound tritium in an animal product to the corresponding concentrations in the animals diet. These concentration ratios are shown to be less subject to

  2. 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

  3. 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

  4. Radionuclide Basics: Tritium

    Science.gov (United States)

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

  5. Tritium isotope fractionation in biological systems and in analytical procedures

    International Nuclear Information System (INIS)

    Kim, M.A.; Baumgaertner, Franz

    1989-01-01

    The organically bound tritium (OBT) is evaluated in biological systems by determining the tritium distribution ratio (R-value), i.e. tritium concentrations in organic substance to cell water. The determination of the R-value always involves isotope fractionation is applied analytical procedures and hence the evaluation of the true OBT -value in a given biological system appears more complicated than hitherto known in the literature. The present work concentrates on the tritium isotope fractionation in the cell water separation and on the resulting effects on the R-value. The analytical procedures examined are vacuum freeze drying under equilibrium and non-equilibrium conditions and azeotropic distillation. The vaporization isotope effects are determined separately in the phase transition of solid or liquid to gas in pure tritium water systems as well as in real biological systems, e.g. corn plant. The results are systematically analyzed and the influence of isotope effects on the R-value is rigorously quantified

  6. 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)

  7. 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

  8. FDMH - The tritium model in RODOS

    International Nuclear Information System (INIS)

    Galeriu, D.; Mateescu, G.; Melintescu, A.; Turcanu, C.; Raskob, W.

    2000-01-01

    Under the auspices of its RTD (Research and Technological Development) Framework Programmes, the European Commission has supported the development of the RODOS (Real-time On-line DecisiOn Support) system for off-site emergency management. The project started in 1989 focusing on PWR/LWR type accidents and using experience from the Chernobyl accident. In 1996 it was realised that tritium should be included in the list of radionuclides, as large tritium sources exist in Europe and to allow a potential expansion of the RODOS system for application on future fusion reactor accidents. The National Institute for Physics and Nuclear Engineering (IFIN-HH) in Romania - in close co-operation with the Research Centre Karlsruhe (FZK) - was charged to develop the tritium module, based on previous experience in environmental tritium modelling and the operation of CANDU reactor-based NPP in Romania (with potential tritium accidents). Tritium, being an isotope of hydrogen, is incorporated immediately in the life cycle and its transport into the biosphere differs considerably from other radionuclides treated by the RODOS system. Concentrations in the individual compartments may change very rapidly (hours) under varying environmental conditions and conversion to organic forms by biochemical and metabolic processes takes place in plants and animals. Consequently, the tritium code in RODOS was developed as a separate module and harmonisation in data sets and interfaces with other food chain modules integrated in RODOS was ensured. Presently, the tritium module - FDMH- is integrated and documented in the RODOS system, delivering time dependent tritium concentration (as tritiated water or organically bound tritium) in plant and animal products, inhalation dose and ingestion dose for various groups of population, after an accident emitting tritiated water and for up to 2520 locations around the source. FDMH incorporates many improved techniques in radiological assessment and makes

  9. 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.

  10. Tritium proof-of-principle pellet injector results

    International Nuclear Information System (INIS)

    Fisher, P.W.; Fehling, D.T.; Gouge, M.J.; Milora, S.L.

    1989-01-01

    The tritium proof-of-principle (TPOP) experiment was built by Oak Ridge National Laboratory (ORNL) to demonstrate the feasibility of forming solid tritium pellets and accelerating them to high velocities for fueling future fusion reactors. TPOP used a pneumatic pipe-gun with a 4-mm-i.d. by 1-m-long barrel. Nearly 1500 pellets were fired by the gun during the course of the experiment; about a third of these were tritium or mixtures of deuterium and tritium. The system also contained a cryogenic 3 He separator that reduced the 3 He level to <0.005%. Pure tritium pellets were accelerated to 1400 m/s. Experiments evaluated the effect of cryostat temperature and fill pressure on pellet size, the production of pellets from mixtures of tritium and deuterium, and the effect of aging on pellet integrity. The tritium phase of these experiments was performed at the Tritium Systems Test Assembly (TSTA) at Los Alamos National Laboratory. About 100 kCi of tritium was processed through the apparatus without incident. 8 refs., 7 figs

  11. Development of organic tritium light technology at Ontario Hydro

    International Nuclear Information System (INIS)

    Mullins, D.F.; Krasznai, J.P.; Mueller, D.A.

    1992-01-01

    Tritium is a by-product of CANDU heavy water reactor operations and is the major contributor to internal dose for plant workers. The Darlington Tritium Removal Facility (DTRF) is decontaminating heavy water by removing tritium and storing it as a metal hydride. In view of the large tritium separation capacity, (24 MCi/a, 888 PBq/a). This paper reports that Ontario Hydro is interested in pursuing markets for the peaceful uses of tritium. One of these peaceful uses is in self-luminous lighting. The state of the art at present is a phosphor coated tube filled with tritium gas. However, safety considerations have restricted the use of these lights to outdoor or essential safety applications. Binding the tritium to a solid non-volatile matrix would increase the safety of tritium lights and allow the use of other phosphors, matrices and construction geometries. Solid, organic based tritium lights were produced using two different polymer matrices. While both these materials produced visible light, the intensity was low and radiolytic damage to the polymers was evident

  12. 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

  13. 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

  14. 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.)

  15. 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)

  16. 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)

  17. 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

  18. Accounting strategy of tritium inventory in the heavy water detritiation pilot plant from ICIT Rm. Valcea

    International Nuclear Information System (INIS)

    Bidica, N.; Stefanescu, I.; Cristescu, I.; Bornea, A.; Zamfirache, M.; Lazar, A.; Vasut, F.; Pearsica, C.; Stefan, I.; Prisecaru, I.; Sindilar, G.

    2008-01-01

    In this paper we present a methodology for determination of tritium inventory in a tritium removal facility. The method proposed is based on the developing of computing models for accountancy of the mobile tritium inventory in the separation processes, of the stored tritium and of the trapped tritium inventory in the structure of the process system components. The configuration of the detritiation process is a combination of isotope catalytic exchange between water and hydrogen (LPCE) and the cryogenic distillation of hydrogen isotopes (CD). The computing model for tritium inventory in the LPCE process and the CD process will be developed basing on mass transfer coefficients in catalytic isotope exchange reactions and in dual-phase system (liquid-vapour) of hydrogen isotopes distillation process. Accounting of tritium inventory stored in metallic hydride will be based on in-bed calorimetry. Estimation of the trapped tritium inventory can be made by subtraction of the mobile and stored tritium inventories from the global tritium inventory of the plant area. Determinations of the global tritium inventory of the plant area will be made on a regular basis by measuring any tritium quantity entering or leaving the plant area. This methodology is intended to be applied to the Heavy Water Detritiation Pilot Plant from ICIT Rm. Valcea (Romania) and to the Cernavoda Tritium Removal Facility (which will be built in the next 5-7 years). (authors)

  19. 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

  20. 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.

  1. Validation of tritium measurements in biological materials

    International Nuclear Information System (INIS)

    Kim, M.A.; Baumgartner, F.

    1988-01-01

    The maximum deviation of experimental R value from its real value, which is defined as the ratio of tissue bound to tissue water tritium, has been calculated and verified experimentally by taking consideration of isotopic fractionation arised in the course of water separation. Experimental procedures examined for the purpose are the azeotropic distillation and lyophilization for the removal of tissue water and the oxidative combustion of organic residue either by thermal process or by low temperature plasma generation. Each procedure optimalized by obviating or correcting isotope effects as well as other sources of error has been tested with mixed standards and biological samples. By washing out the exchangeable tritium and also physically bound tritium, the precision and accuracy of R values are further improved

  2. 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

  3. Tritium permeation and recovery

    International Nuclear Information System (INIS)

    Bond, R.A.; Hamilton, A.M.

    1987-01-01

    The paper is an appendix to a study of the reactor relevance of the NET design concept. The latter study examines whether the technologies and design principles proposed for NET can be directly extrapolated to a demonstration (DEMO) reactor. In this appendix, tritium transport in the DEMO breeding blanket is considered with emphasis on the permeation rate from the lithium-lead breeder into the coolant. A computational model used to calculate the tritium transport in the breeder blanket is described. Results are reported for the tritium transport in the NET/INTOR type blanket as well as the DEMO blanket in order to provide a comparison. In addition, results are presented for the helium coolant tritium extraction analysis. (U.K.)

  4. 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

  5. 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.)

  6. Tritium-v. 2

    International Nuclear Information System (INIS)

    1987-01-01

    Several bibliographical references about tritium are shown. The following aspects are presented: properties, analysis, monitoring, dosimetry reactions, labelling, industrial production, radiological protection, applications to science, technology and industry and some processes to obtain the element. (E.G.) [pt

  7. 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.

  8. 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.

  9. Binder-free Na-mordenite pellets for tritium processing

    International Nuclear Information System (INIS)

    Toci, F.; Viola, A.; Edwards, R.A.H.; Mencarelli, T.; Brossa, P.

    1995-01-01

    Gas separation systems based on adsorption on zeolites are used in various applications involving tritium: air and inert gas detritiation, purification of Q 2 and Q 2 O, and isotope separation. Differential adsorption processes are attractive because efficient separation can be combined with small plant dimensions, low energy consumption and a small tritium inventory. Zeolites are the usual choice for the adsorbate because they combine high adsorption capacity with high selectivity and stability. However, commercial pellets show appreciable tritium retention due to inappropriate activation procedures or the presence of a binder. In this paper we report a research study aimed at producing a pelletized zeolite without binder (self-bound) with low tritium retention. (orig.)

  10. Thin film tritium dosimetry

    Science.gov (United States)

    Moran, Paul R.

    1976-01-01

    The present invention provides a method for tritium dosimetry. A dosimeter comprising a thin film of a material having relatively sensitive RITAC-RITAP dosimetry properties is exposed to radiation from tritium, and after the dosimeter has been removed from the source of the radiation, the low energy electron dose deposited in the thin film is determined by radiation-induced, thermally-activated polarization dosimetry techniques.

  11. Management of tritium wastes

    International Nuclear Information System (INIS)

    Kisalu, J.; Mellow, D.G.; Pennington, J.D.; Thompson, H.M.; Wood, E.

    1991-07-01

    This work provides a review of the management of tritium wastes with particular reference to current practice, possible alternatives and to the implications of any alternatives considered. It concludes that reduction in UK emissions from nuclear industry is feasible but at a cost out of all proportion to the reduction in dose commitment achievable. Commercial usage of tritium involves importation at several times the UK nuclear production level although documentation is sparse. (author)

  12. PRODUCTION OF TRITIUM

    Science.gov (United States)

    Jenks, G.H.; Shapiro, E.M.; Elliott, N.; Cannon, C.V.

    1963-02-26

    This invention relates to a process for the production of tritium by subjecting comminuted solid lithium fluoride containing the lithium isotope of atomic mass number 6 to neutron radiation in a self-sustaining neutronic reactor. The lithium fiuoride is heated to above 450 deg C. in an evacuated vacuum-tight container during radiation. Gaseous radiation products are withdrawn and passed through a palladium barrier to recover tritium. (AEC)

  13. Reassessment of tritium dose coefficients for the general public

    International Nuclear Information System (INIS)

    Melintescu, A.; Galeriu, D.; Takeda, H.

    2007-01-01

    Concerns of increased risk from tritium intake by humans have been claimed in the past. The arguments concerning the radiobiological effectiveness of tritium, its longer retention in the human body and the presence of tritium in the DNA hydration shell are analysed in this paper. A biokinetic model for tritiated water and organically bound tritium retention in the human body is used, based on a common approach for mammals using energy and hydrogen metabolism and tested separately with animal experiments. Extension to this model to humans considers the increased role of the brain, food quality and unique growth patterns of humans. Various ages and genders for Caucasians are considered. For an intake of tritium in organic forms in the diet, the retention for the female is of about a factor 2 compared with ICRP recommendations. Effective dose coefficients are estimated to be about a factor of 2 to 3 higher than those of the ICRP. (authors)

  14. TSTA loop operation with 100 grams-level of tritium

    International Nuclear Information System (INIS)

    Yoshida, Hiroshi; Fukui, Hiroshi; Hirata, Shingo

    1988-12-01

    A fully integrated loop operation test of Tritium systems Test Assembly (TSTA) with 107 grams of tritium was completed at Los Alamos National Laboratory (LANL) in June, 1988. In this test, a compound cryopump with a charcoal panel was incorporated into the main process loop for the first time. The objectives were (i) to demonstrate the compound cryopump system with different flow rates and impurities, (ii) to demonstrate the regeneration of the compound cryopump system, (iii) to accumulate operating experience with other process systems such as the fuel cleanup system, the isotope separation system, the tritium supply and recovery system, etc. and (iv) to improve the data-base on TSTA safety systems such as the secondary containment system, tritium waste treatment system and tritium monitoring system. This report briefly describes characteristics of the main subsystems observed during the milestone run. (author)

  15. 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

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

    Energy Technology Data Exchange (ETDEWEB)

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

    1995-02-01

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

  17. 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)

  18. 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

  19. Influence of neutron irradiation on the tritium retention in beryllium

    Energy Technology Data Exchange (ETDEWEB)

    Rolli, R.; Ruebel, S.; Werle, H. [Forschungszentrum Karlsruhe, Inst. fuer Neutronenphysik und Reaktortechnik, Karlsruhe (Germany); Wu, C.H.

    1998-01-01

    Carbon-based materials and beryllium are the candidates for protective layers on the components of fusion reactors facing plasma. In contact with D-T plasma, these materials absorb tritium, and it is anticipated that tritium retention increases with the neutron damage due to neutron-induced traps. Because of the poor data base for beryllium, the work was concentrated on it. Tritium was loaded into the samples from stagnant T{sub 2}/H{sub 2} atmosphere, and afterwards, the quantity of the loaded tritium was determined by purged thermal annealing. The specification of the samples is shown. The samples were analyzed by SEM before and after irradiation. The loading and the annealing equipments are contained in two different glove boxes with N{sub 2} inert atmosphere. The methods of loading and annealing are explained. The separation of neutron-produced and loaded tritium and the determination of loaded tritium in irradiated samples are reported. Also the determination of loaded tritium in unirradiated samples is reported. It is evident that irradiated samples contained much more loaded tritium than unirradiated samples. The main results of this investigation are summarized in the table. (K.I.)

  20. Retrospective evaluation of tritium fallout by tree-ring analysis

    International Nuclear Information System (INIS)

    Kozak, K.; Biro, T.; Golder, F.; Rank, D.; Rajner, V.; Staudner, F.

    1993-01-01

    Tritium analyses of tree-ring cellulose were made to test its suitability for retrospective evaluation of a local tritium fallout. Several spruce trees were taken from an Austrian alpine area where tritium contamination of May 1974 precipitation had been detected. Wood from the annual growth rings of 1973, 1974 and 1975 was separated and the cellulose extracted. After isotopic equilibration with dead water, cellulose was combusted to yield water, whose tritium concentration was measured by liquid scintillation counting. Rigorous statistical treatment proved the significance of the increased tritium concentration caused by the tritium anomaly, which occurred during the growing season. The long-term trends of local atmospheric tritium, including the 1974 peak, were also well reflected by analysis of a 24-year ring sequence from a single tree in the contaminated area. The tritium data gained by the given method can be used at present qualitatively and a better understanding of the possible sources of contamination is required in order that the quantitative criteria be satisfied. (Author)

  1. 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

  2. 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

  3. Tritium emissions reduction facility (TERF)

    International Nuclear Information System (INIS)

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

    1993-01-01

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

  4. Tritium 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

  5. Tritium Systems Test Facility

    International Nuclear Information System (INIS)

    Cafasso, F.A.; Maroni, V.A.; Smith, W.H.; Wilkes, W.R.; Wittenberg, L.J.

    1978-01-01

    This TSTF proposal has two principal objectives. The first objective is to provide by mid-FY 1981 a demonstration of the fuel cycle and tritium containment systems which could be used in a Tokamak Experimental Power Reactor for operation in the mid-1980's. The second objective is to provide a capability for further optimization of tritium fuel cycle and environmental control systems beyond that which is required for the EPR. The scale and flow rates in TSTF are close to those which have been projected for a prototype experimental power reactor (PEPR/ITR) and will permit reliable extrapolation to the conditions found in an EPR. The fuel concentrations will be the same as in an EPR. Demonstrations of individual components of the deuterium-tritium fuel cycle and of monitoring, accountability and containment systems and of a maintenance methodology will be achieved at various times in the FY 1979-80 time span. Subsequent to the individual component demonstrations--which will proceed from tests with hydrogen (and/or deuterium) through tracer levels of tritium to full operational concentrations--a complete test and demonstration of the integrated fuel processing and tritium containment facility will be performed. This will occur near the middle of FY 1981. Two options were considered for the TSTF: (1) The modification of an existing building and (2) the construction of a new facility

  6. Tritium analysis at TFTR

    International Nuclear Information System (INIS)

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

    1995-01-01

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

  7. Tritium concentration in the heavy water upgrading plants

    International Nuclear Information System (INIS)

    Croitoru, C.; Pop, F.; Titescu, Gh.; Dumitrescu, M.; Ciortea, C.; Stefanescu, I.; Peculea, M.; Pitigoi, Gh.; Trancota, D. . E-mail of corresponding author: croitoru@icsi.ro; Croitoru, C.)

    2005-01-01

    In the course of time heavy water used in CANDU nuclear power plants, as moderator or coolant, degrades, as a result of its impurification with light water and tritium. Concentration diminution below 99.8% mol for moderator and 99.75% mol for coolant causes an inefficient functioning of CANDU reactor. By isotopic distillation, light water is removed. Simultaneously tritium concentration takes place. The heavy water upgrading plant from Cernavoda is an isotopic separation cascade with two stages. The paper presents, for this plant, a theoretical study of the tritium concentration. (author)

  8. 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)

  9. Radiological safety system based on real-time tritium-in-air monitoring indoor and in effluents

    International Nuclear Information System (INIS)

    Bidica, Nicolae; Sofalca, Nicolae; Balteanu, Ovidiu-Ioan; Stefan, Ioana-Iuliana

    2007-01-01

    In this paper we describe an improved real-time tritium monitoring system designed for Heavy Water Detritiation Pilot Plant of National Institute for Cryogenics and Isotopes Separation, Rm. Valcea, Romania. The system consists of three fixed tritium-in-air monitors which measure continuously tritium-in-air concentration (in both species: vapour and gas) in working areas and gaseous effluents. Portable tritium monitors with ionization chamber, and tritium-in-air collector combined with liquid scintillation counter method are also used to supplement fixed instrument measurements. The main functions of tritium monitoring system are: to measure tritium-in air concentration in working areas and gaseous effluents; to alarm the personnel if tritium concentration thresholds are exceeded; to integrate tritium activity released to the environment during a week and to cut off normal ventilation when the activity threshold is exceeded and start the air cleaning system. Now, several especial functions have been added, so that by using appropriate conversion factors, the tritium monitoring system is able to estimate the effective dose rate before starting an activity into the monitored area, during this activity, or soon as the activity was finished. Another new function has been added by coupling tritium-in-air monitoring system with control access system. This is very useful for quick estimation of tritium doses. For routine dosimetric survey, one the internal dose for individuals by measuring tritium in urine is estimated. With all these features our tritium monitoring system is really a safety system for personnel and for environment. (authors)

  10. Assessment of the cryogenic distillation system in Cernavoda tritium removal facility

    International Nuclear Information System (INIS)

    Pasca, Gheorghe; Draghia, Mirela; Porcariu, Florina; Ana, George

    2010-01-01

    Full text: This paper aims at presenting an assessment of the Cryogenic Distillation system (CD) in the Cernavoda Tritium Removal Facility (CTRF). The cryogenic distillation system is one of the key components of the CTRF which comprises other systems as: the liquid phase catalytic exchange system, designed to transfer tritium from heavy water to a deuterium stream to be fed into the CD system; the atmosphere detritiation system; the tritium recovery system; the tritium/hydrogen monitoring system; the central interlocking system; the tritium extraction and storage system. Thus, the need to build a tritium separation and recovery system results from economic opportunities offered both by heavy water reuse and tritium production, but, at the same time, it offers an alternative for the storage of tritiated heavy water as radioactive waste. (authors)

  11. Tritium - is it underestimated

    International Nuclear Information System (INIS)

    Whitlock, G.D.

    1980-01-01

    Practical experience in the use of the Whitlock Tritium Meter in various laboratories and industrial establishments throughout the world has shown that:-a) Measurements by smear/wipe tests can often be in error by three orders of magnitude or more; b) Sub-visual surface scratches (8μ deep) are radiologically important; c) Volatile forms of tritium exist in 20% to 30% of establishments visited. It is concluded that a) the widespread use of smear/wipe techniques for the assessment of 3 H surface contamination based on the assumption that 10% of removable activity is collected by the smear/wipe should be re-examined and b) tritium surface contamination assessed as 'fixed' can contain volatile fractions with a hazard potential which may be considerably greater than the hazard from removable activity at present covered by maximum permissible level recommendations. (H.K.)

  12. Tritium in HTR systems

    International Nuclear Information System (INIS)

    Steinwarz, W.

    1987-07-01

    Starting from the basis of the radiological properties of tritium, the provisions of present-day radiation protection legislation are discussed in the context of the handling of this radionuclide in HTR plants. Tritium transportation is then followed through from the place of its creation up until the sink, i.e. disposal and/or environmental route, and empirical values obtained in experiments and in plant operation translated into guidelines for plant design and planning. The use of the example of modular HTR plants permits indication that environmental contamination via the 'classical' routes of air and water emissions, and contamination of products, and resulting consumer exposure, are extremely low even on the assumption of extreme conditions. This leads finally to a requirement that the expenditure for implementation of measures for further reduction of tritium activity rates be measured against low radiological effect. (orig.) [de

  13. Electrochemical measurement of tritium and hydrogen permeation through iron membranes

    International Nuclear Information System (INIS)

    Hagi, Hideki; Hayashi, Yasunori

    1988-01-01

    Permeation rates of tritium and hydrogen through iron were measured by the electrochemical method in which an aqueous solution containing 3.7 x 10 12 Bq/m 3 tritium was used as a cathodic electrolyte. Tritium and hydrogen were introduced from one side of a specimen by cathodic polarization with a constant current density, while at the other side of the specimen the permeated tritium and hydrogen were extracted by potentiostatical ionization. Nearly all of the potentiostatic current of the extraction side stands for the ionization of hydrogen, because the concentration of tritium in the cathodic electrolyte is very small. 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. The separation factor for permeation obtained under steady state conditions (the ratio of permeation rates of hydrogen to tritium divided by the ratio of the concentration of hydrogen to tritium in the charging electrolyte) is 12 at 288 K. This value is independent of cathodic current density. Diffusion coefficients of tritium (D T ) and hydrogen (D H ) in iron were determined from the time lag of tritium and hydrogen permeation. For annealed specimens at 286 K, D T = 9 x 10 -10 m 2 /s and D H = 4 x 10 -9 m 2 /s, and for 9% cold-worked specimens at 284 K, D T = 3 x 10 -10 m 2 /s and D H = 4 x 10 -10 m 2 /s. (author)

  14. Electrochemical measurement of tritium and hydrogen permeation through iron membranes

    International Nuclear Information System (INIS)

    Hagi, Hideki; Hayashi, Yasunori

    1987-01-01

    Permeation rates of tritium and hydrogen through iron were measured by the electro-chemical method in which an aqueous solution containing 3.7 x 10 12 Bq/m 3 tritium was used as a cathodic electrolyte. Tritium and hydrogen were introduced from one side of a specimen by cathodic polarization with a constant current density, while at the other side of the specimen the permeated tritium and hydrogen were extracted by potentiostatical ionization. Nearly all of the potentiostatic current on the extraction side is produced by the ionization of hydrogen, because the concentration of tritium in the cathodic electrolyte is very small. The amount of permeated hydrogen was obtained by integrating the potentiostatic current, and that of permeated tritium was determined by measuring the radioactivity of the electrolyte sampled from the anodic side. The separation factor for permeation obtained under steady state conditions (the ratio of permeation rates of hydrogen to tritium divided by the ratio of the concentration of hydrogen to tritium in the cathodic electrolyte) is 12 at 288 K. This value is independent of cathodic current density. Diffusion coefficients of tritium (D T ) and hydrogen (D H ) in iron were determined from the tritium and hydrogen permeation by using time lag technique. For annealed iron at 286 K, D T = 9 x 10 -10 m 2 /s and D H = 4 x 10 -9 m 2 /s, and for 9 % cold-worked iron at 284 K, D T = 3 x 10 -10 m 2 /s and D H = 4 x 10 -10 m 2 /s. (author)

  15. Design of a tritium decontamination workstation based on plasma cleaning

    International Nuclear Information System (INIS)

    Antoniazzi, A.B.; Shmayda, W.T.; Fishbien, B.F.

    1993-01-01

    A design for a tritium decontamination workstation based on plasma cleaning is presented. The activity of tritiated surfaces are significantly reduced through plasma-surface interactions within the workstation. Such a workstation in a tritium environment can routinely be used to decontaminate tritiated tools and components. The main advantage of such a station is the lack of low level tritiated liquid waste. Gaseous tritiated species are the waste products with can with present technology be separated and contained

  16. Atmospheric tritium. Measurement and application

    International Nuclear Information System (INIS)

    Frejaville, Gerard

    1967-02-01

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

  17. Handling of tritium at TFTR

    International Nuclear Information System (INIS)

    Pierce, C.W.; Howe, H.J.; Yemin, L.; Lind, K.

    1977-01-01

    Some of the engineering approaches taken at TFTR for the tritium control systems are discussed as the requirements being placed on the tritium systems by the operating scenarios of the Tokamak. The tritium control systems presently being designed for TFTR will limit the annual release to the environment to less than 100 curies

  18. Tritium effluent removal system

    International Nuclear Information System (INIS)

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

    1978-01-01

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

  19. Tritium removal from contaminated water via infrared laser multiple-photon dissociation

    International Nuclear Information System (INIS)

    Maienschein, J.L.; Magnotta, F.; Herman, I.P.; Aldridge, F.T.; Hsiao, P.

    1983-01-01

    Isotope separation by means of infrared-laser multiple-photon dissociation offers an efficient way to recover tritium from contaminated light or heavy water found in fission and fusion reactors. For tritium recovery from heavy water, chemical exchange of tritium into deuterated chloroform is followed by selective laser dissociation of tritiated chloroform and removal of the tritiated photoproduct, TCl. The single-step separation factor is at least 2700 and is probably greater than 5000. Here we present a description of the tritium recovery process, along with recent accomplishments in photochemical studies and engineering analysis of a recovery system

  20. Monitoring of tritium

    Science.gov (United States)

    Corbett, James A.; Meacham, Sterling A.

    1981-01-01

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

  1. Operation of the TSTA (Tritium Systems Test Assembly) with 100 gram tritium

    International Nuclear Information System (INIS)

    Sherman, R.H.; Bartlit, J.R.

    1988-01-01

    In March of 1988 full operation of the 4-column isotope separation system (ISS) was realized in runs that approximated the design load of tritium. Previous operations had been fraught with operating difficulties principally due to external systems. This report will examine the recent highly successful 6-day period of operation. During this time the system was cooled from room temperature, loaded with hydrogen isotopes including 109 grams of tritium, integrated with the transfer pumping, impurity injection, and impurity removal systems, as well as the remote computer control system. At the end of the operation 12 grams of tritium having a measured purity of 99.987% (remainder deuterium) were offloaded from the system. Observed profiles in the columns in general agree with computer models. A Height Equivalent to a Theoretical Plate (HETP) of 5.0 cm is confirmed. 3 refs., 5 figs

  2. Production sources and management of tritium generated by nuclear facilities. Works reporting from the reflection group 'tritium defense-in-depth'

    International Nuclear Information System (INIS)

    2001-01-01

    This report synthesizes current knowledge of tritium, its sources of tritium and its behavior in reactors and nuclear facilities. In addition, liquid and gaseous tritiated releases and the processes of separation and possible trapping of this radionuclide are displayed. This report also provides elements of reflection on the management of tritium produced today by these facilities, both in France and abroad. It presents insights on the relevance of current management modes of tritiated liquid and solid waste and also on the associated measures to reduce releases of tritium into the environment. (author)

  3. 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)

  4. 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

  5. The impact of tritium solubility and diffusivity on inventory and permeation in liquid breeder blankets

    International Nuclear Information System (INIS)

    Caorlin, M.; Gervasini, G.; Reiter, F.

    1988-01-01

    The authors reviewed hydrogen solubility and diffusivity data for liquid lithium-based compounds which are potential breeding blanket materials in NET-type fusion devices. These data have been used to assess tritium permeation and inventory in separately cooled NET blankets and in self cooled blankets with a vanadium first wall. The results for the separately cooled NET-liquid breeder show that tritium permeation is negligible for lithium, a serious problem for Pb-17Li and a critical one for Flibe. The total tritium inventory is lowest in lithium, high in Pb-17Li and very high in Flibe. The high tritium partial pressure for Flibe or Pb-17Li can be reduced in a self cooled blanket with a vanadium first wall. Permeation into the plasma reduces the blanket tritium inventory and permeation. Tritium recovery can be combined with the plasma exhaust

  6. Tritium breeding materials

    International Nuclear Information System (INIS)

    Hollenberg, G.W.; Johnson, C.E.; Abdou, M.

    1984-03-01

    Tritium breeding materials are essential to the operation of D-T fusion facilities. Both of the present options - solid ceramic breeding materials and liquid metal materials are reviewed with emphasis not only on their attractive features but also on critical materials issues which must be resolved

  7. Tritium breeding materials

    International Nuclear Information System (INIS)

    Hollenberg, G.W.; Johnson, C.E.; Abdou, M.A.

    1984-01-01

    Tritium breeding materials are essential to the operation of D-T fusion facilities. Both of the present options - solid ceramic breeding materials and liquid metal materials are reviewed with emphasis not only on their attractive features but also on critical materials issues which must be resolved

  8. 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

  9. 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.)

  10. 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

  11. 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

  12. Tritium determination in water

    International Nuclear Information System (INIS)

    Gavini, Ricardo M.

    2008-01-01

    An analytical procedure for the determination of tritium in water is described in this paper. The determination is carried out in presence of other radionuclides, such as Fe-55, Ni-63, Mn-54, Zn-65, Co-60, Cd-109, Sr-90, Cs-134 and Cs-137. The method consists in a simple distillation stage prior to measurement by liquid scintillation counting. The samples containing beta and gamma emitters are conditioned with a (NO 3 ) 2 Pb solution and Na(OH) up to pH = 7 - 8. This produces lead hydroxide precipitation that allows fixing volatile elements, which could be transported together with tritium, and may increase the extinction degree of the sample or interfere with the counting process. Special attention must be paid if presence of Fe-55 (E max ∼ 5.95 keV) is suspected as it might not be distinguished from tritium (E max ∼ 18 keV), leading to an overestimation of tritium activity. Different tests were carried to obtain the optimum method conditions, to achieve the purification of the tritium and a pH near to 7 in the distilled. The detection limit (2σ) was 8.0 Bq/l and the distillation performance was 98.3 %. This technique was applied to water samples containing Fe-55 and other gamma radionuclides in 1M hydrochloric acid media in successive Environmental Measurements Laboratory (EML), U.S. Department of Energy (DOE) intercomparison programs. The results obtained were very satisfactory and are presented in this paper. (author)

  13. A methodology for determination of tritium inventory to the heavy water detritiation pilot plant from ICIT Rm. Valcea

    International Nuclear Information System (INIS)

    Bidica, N.; Stefanescu, I.; Bornea, A.; Zamfirache, M.; Lazar, A.; Vasut, F.; Pearsica, C.; Stefan, I.; Cristescu, I.; Prisecaru, I.; Sindilar, G.

    2007-01-01

    Full text: In this paper we present a methodology for determination of tritium inventory in a tritium removal facility. The method proposed is based on the developing of computing models for accountancy of the mobile tritium inventory in the separation processes of the stored tritium and of the trapped tritium inventory in the structure of the process system components. The configuration of the detritiation process is a combination of isotope catalytic exchange between water and hydrogen (LPCE) and the cryogenic distillation of hydrogen isotopes (CD). The computing model for tritium inventory in the LPCE process and the CD process will be developed based on mass transfer coefficients in catalytic isotope exchange reactions and in dual-phase system (liquid-vapour) of hydrogen isotopes distillation process. Accounting of tritium inventory stored in metallic hydride will be based on in-bed calorimetry. Estimation of the trapped tritium inventory can be made by subtraction of the mobile and stored tritium inventories from the global tritium inventory of the plant area. Determinations of the global tritium inventory of the plant area will be made on a regular basis by measuring any tritium amount entering or leaving the plant area. This methodology is intended to be applied to the Heavy Water Detritiation Pilot Plant from ICIT Rm. Valcea (Romania) and at the Cernavoda Tritium Removal Facility (which will be built in the next 5-7 years). (authors)

  14. 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.

  15. Tritium systems concepts for the next European torus (NET)

    International Nuclear Information System (INIS)

    Sood, S.K.; Bagli, K.S.; Busigin, A.; Kveton, O.K.; Dombra, A.H.; Miller, A.I.

    1986-09-01

    The study deals with the design of the various tritium processing facilities that will be required for the Next European Torus (NET) design. The reference data for the design of the NET Tritium Systems was provided by the NET team. Significant achievements of this study were: (a) Identification of new ways of handling some problems for example: 1) Recovery of tritium from the helium purge of the lithium-ceramic blanket using a novel Adsoprtion and Catalytic Exchange Process, 2) A new way of combining fuel component separation and coolant water detritiation using cryogenic distillation, 3) The use of parasitic refrigeration for the cryogenic isotope separation, 4) Tritium extraction from effluent gas streams at their respective sources, 5) Attempt to eliminate the need for Air Cleanup Systems. (b) Identification of uncertainties, for example: composition of plasma exhaust, required helium purge rate of Li-Pb for tritium recovery, uncertainty in requirements for decontaminating blanket sectors, etc. (c) Review of ways to limit tritium permeation into steam by swamping with hydrogen and to provide quantitative estimates for this permeation

  16. Methods of detecting tritium in gases and liquids

    Energy Technology Data Exchange (ETDEWEB)

    Petr, I

    1977-07-01

    Tritium mainly occurs in gases in two chemical forms, i.e., as water vapour (HTO) or elemental hydrogen (HT). Two methods for tritium gas measuring are described. The first consists in the use of an ionization chamber or a proportional counter with the sample sucked in through a filter to the detector working volume. The second consists in the separation of tritium (in the form of HTO) from the gas sample by sorption on silica gel or on molecular sieves and its detection using a liquid or a plastic scintillation detector. Tritium in the form of HT and gaseous organic tritium compounds are determined using the same measuring method after oxidation of the gaseous samples to HTO by burning. A description is given of detectors and measuring methods. Tritium in liquids mainly occurs in the form of tritiated water (HTO). The most commonly used method of tritium detection in liquids is the application of liquid scintillation detectors in which the sample is dissolved or suspended and measured with two photomultipliers in time-coincidence connection. The main advantage of liquid scintillators is the possibility to achieve the 4..pi.. measurement geometry. The methods of calibration and of checking the stability of a measuring system with liquid scintillators are described as are the applications of plastic scintillators in measuring tritium in liquids. Plastic scintillators are less costly in operation and show a more rapid response but their sensitivity is lower. The threshold values of activity are shown in dependence on the detector applied, the chemical form of tritium and the sampling method.

  17. Tritium production in thorium by 135 MeV protons

    International Nuclear Information System (INIS)

    Lefort, M.; Simonoff, G.; Tarrago, X.; Bibron, R.

    1960-01-01

    We have measured the cross-section of tritium production by bombardment of thorium by 135 MeV protons in the Orsay synchro-cyclotron. The tritium was separated from the targets by heating in a graphite crucible with a high-frequency generator, under hydrogen gas pressure. Tritiated water was synthesised and the tritium was measured with liquid scintillator. A value of 19.5 ± 0.05 mbarns was obtained for the tritium-cross section and ten percent of tritons have energies higher than 35 MeV. This large cross-section is attributed to a double pick-up process. Reprint of a paper published in Le Journal de Physique et le Radium, t. 20, p. 959, dec 1959 [fr

  18. 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

  19. 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.)

  20. A low inventory adsorptive process for tritium extraction and purification

    International Nuclear Information System (INIS)

    Keefer, B.; Bora, B.; Chew, M.; Rump, M.; Kveton, O.K.

    1990-08-01

    The fuel cycles of future fusion power systems present a diverse spectrum of challenges to gas separation technology, for extraction, concentration, purification and confinement of tritium in fusion fuel cycles. Economic and safety factors motivate process design for minimum tritium inventory, functional simplicity, and overall reliability. A new gas separation process with some features of interest to fusion has been demonstrated under the auspices of the Canadian Fusion Fuels Technology Project. This process (Thermally Coupled Pressure Swing Adsorption or 'TCPSA') is potentially applicable to several fusion applications for separation purification of hydrogen, notably for tritium extraction from breeder blanket purge helium. Recent experimental tests have been directed toward fusion applications, primarily extraction and concentration of tritium-rich hydrogen from the blanket purge helium stream, and also considering purification of this and other hydrogen isotope streams such as the plasma exhaust. For example, hydrogen at 0.1% concentration in helium has been extracted in a TCPSA module operating at 195 K, with the process performed in a single working space to achieve simultaneous high extraction and concentration of the hydrogen. With methane or carbon oxides as the impurities, substantially complete separation is achieved by the same apparatus at ambient temperature. Engineering projections for scale-up to ITER blanket purge extraction and purification applications indicate a low working inventory of tritium

  1. 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.)

  2. Universal tritium transmitter

    International Nuclear Information System (INIS)

    Cordaro, J. V.; Wood, M.

    2008-01-01

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

  3. Five years of tritium handling experience at the Tritium Systems Test Assembly

    International Nuclear Information System (INIS)

    Carlson, R.V.

    1989-01-01

    The Tritium Systems Test Assembly (TSTA) at Los Alamos National Laboratory is a facility designed to develop and demonstrate, in full scale, technologies necessary for safe and efficient operation of tritium systems required for tokamak fusion reactors. TSTA currently consists of systems for evacuating reactor exhaust gas with compound cryopumps; for removing impurities from plasma exhaust gas and recovering the chemically-combined tritium; for separating the isotopes of hydrogen; for transfer pumping; or storage of hydrogen isotopes; for gas analysis; and for assuring safety by the necessary control, monitoring, and tritium removal from effluent streams. TSTA also has several small scale experiments to develop and test new equipment and processes necessary for fusion reactors. In this paper, data on component reliability, failure types and rates, and waste quantities are presented. TSTA has developed a Quality Assurance program for preparing and controlling the documentation of the procedures required for the design, purchase, and operation of the tritium systems. Operational experience under normal, abnormal, and emergency conditions is presented. One unique aspect of operations at TSTA is that the design personnel for the TSTA systems are also part of the operating personnel. This has allowed for the relatively smooth transition from design to operations. TSTA has been operated initially as a research facility. As the system is better defined, operations are proceeding toward production modes. The DOE requirements for the operation of a tritium facility like TSTA include personnel training, emergency preparedness, radiation protection, safety analysis, and preoperational appraisals. The integration of these requirements into TSTA operations is discussed. 4 refs., 3 figs., 3 tabs

  4. Tritium concentration monitor

    International Nuclear Information System (INIS)

    Shono, Kosuke.

    1991-01-01

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

  5. Metabolism of organically bound tritium

    International Nuclear Information System (INIS)

    Travis, C.C.

    1984-01-01

    The classic methodology for estimating dose to man from environmental tritium ignores the fact that organically bound tritium in foodstuffs may be directly assimilated in the bound compartment of tissues without previous oxidation. We propose a four-compartment model consisting of a free body water compartment, two organic compartments, and a small, rapidly metabolizing compartment. The utility of this model lies in the ability to input organically bound tritium in foodstuffs directly into the organic compartments of the model. We found that organically bound tritium in foodstuffs can increase cumulative total body dose by a factor of 1.7 to 4.5 times the free body water dose alone, depending on the bound-to-loose ratio of tritium in the diet. Model predictions are compared with empirical measurements of tritium in human urine and tissue samples, and appear to be in close agreement. 10 references, 4 figures, 3 tables

  6. A prototype wearable tritium monitor

    International Nuclear Information System (INIS)

    Surette, R. A.; Dubeau, J.

    2008-01-01

    Sudden unexpected changes in tritium-in-air concentrations in workplace air can result in significant unplanned exposures. Although fixed area monitors are used to monitor areas where there is a potential for elevated tritium in air concentrations, they do not monitor personnel air space and may require some time for acute tritium releases to be detected. There is a need for a small instrument that will quickly alert staff of changing tritium hazards. A moderately sensitive tritium instrument that workers could wear would bring attention to any rise in tritium levels that were above predetermined limits and help in assessing the potential hazard therefore minimizing absorbed dose. Hand-held instruments currently available can be used but require the assistance of a fellow worker or restrict the user to using only one hand to perform some duties. (authors)

  7. Effects of tritium in elastomers

    International Nuclear Information System (INIS)

    Zapp, P.E.

    1982-01-01

    Elastomers are used as flange gaskets in the piping system of the Savannah River Plant tritium facilities. A number of elastomers is being examined to identify those compounds more radiation-resistant than the currently specified Buna-N rubber and to study the mechanism of tritium radiation damage. Radiation resistance is evaluated by compression set tests on specimens exposed to about 1 atm tritium for several months. Initial results show that ethylene-propylene rubber and three fluoroelastomers are superior to Buna-N. Off-gassing measurements and autoradiography show that retained surface absorption of tritium varies by more than an order of magnitude among the different elastomer compounds. Therefore, tritium solubility and/or exchange may have a role in addition to that of chemical structure in the damage process. Ongoing studies of the mechanism of radiation damage include: (1) tritium absorption kinetics, (2) mass spectroscopy of radiolytic products, and (3) infrared spectroscopy

  8. 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.

  9. 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

  10. Biological effects of tritium

    International Nuclear Information System (INIS)

    Nieto, M.

    1985-01-01

    The aim of this project is to study the thermal effects on proliferation activity in the intestinal epithelium of the goldfish acclimated at different temperatures (stationary state). The cell division occurs only at certain phases of the circadian cycle when the proliferative activity is synchronized or trained by an environmental factor such as light-dark cycle. Another aspect of the project is the study of the biological effects, non-stochastic, on cell kinetics in animals chronically exposed to low dose rates or tritium and gamma rays from 60 CO, used as a standard radiation. The influence on the accumulated dose per cell and cycle cell in function of the duration of the cell cycle at different acclimation temperatures should be considered. To calculate the risk of tritium contamination from nuclear power plants (radiation exposure), the organic tissue-bond is of decisive importance due to the long turnover of the organic tissue-bond in organisms favouring transport of tritium to other organisms of the ecosystem and to man. (author)

  11. Reconstruction of tritium release history from contaminated groundwater using tree ring analysis

    International Nuclear Information System (INIS)

    Kalin, R.M.; Murphy, C.E. Jr.; Hall, G.

    1995-01-01

    The history of tritium releases to the groundwater from buried waste was reconstructed through dendrochronology. Wood from dated tree rings was sectioned from a cross-section of a tree that was thought to tap the groundwater. Cellulose was chemically separated from the wood. The cellulose was combusted and the water of combustion collected for liquid scintillation counting. The tritium concentration in the rings rose rapidly after 1972 which was prior to the first measurements made in this area. Trends in the tritium concentration of water outcropping to the surface are similar to the trends in tritium concentration in tree rings. 14 refs., 3 figs

  12. Method and equipment to extract and recover tritium from light and heavy water

    International Nuclear Information System (INIS)

    Butler, J.P.; Hammerli, M.M.

    1979-01-01

    A combined electrolysis-catalysis exchange process is proposed to extract tritium, with the aim of being able to reduce the tritium value in the heavy water moderation and cooling system of nuclear power plants. The tritium-contained water is brought into contact in a catalyst column in countercurrent with electrolytically produced hydrogen in this process, the hydrogen is then fed to a catalyst-containing separation column whilst the tritium-contained water flows to the electrolysis cell which produces the hydrogen gas. The process is described in detail. (UWI) [de

  13. Tritium removal and retention device

    International Nuclear Information System (INIS)

    Boyle, R.F.; Durigon, D.D.

    1980-01-01

    A device is provided for removing and retaining tritium from a gaseous medium, and also a method of manufacturing the device. The device, consists of an inner core of zirconium alloy, preferably Zircaloy-4, and an outer adherent layer of nickel which acts as a selective and protective window for passage of tritium. The tritium then reacts with or is absorbed by the zirconium alloy, and is retained until such time as it is desirable to remove it during reprocessing. (auth)

  14. An overview of tritium production

    International Nuclear Information System (INIS)

    He Kaihui; Huang Jinghua; Feng Kaiming

    2002-01-01

    The characteristics of three types of proposed tritium production facilities, fissile type, accelerator production tritium (APT), and fusion type, are presented. The fissile reactors, especially commercial light water reactor, use comparatively mature technology and are designed to meet current safety and environmental guidelines. Conversely, APT shows many advantages except its rather high cost, while fusion reactors appear to offer improved safety and environmental impact, in particular, tritium production based on the fusion-based neutron source. However, its cost keeps unknown

  15. Tritium safety issues for TFCX

    International Nuclear Information System (INIS)

    Reilly, H.J.; Piet, S.J.; Merrill, B.J.

    1985-01-01

    Estimated tritium releases from the Tokamak Fusion Core Experiment are compared to the expected limits. A reaction kinetics model is described that predicts the conversion of tritium to the oxide form in free space. An analysis of the required capacity of the Emergency Tritium Cleanup System is also presented. The conclusions of this work are expected to be applicable to other experimental fusion devices that are now being considered

  16. 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

  17. 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

  18. 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)

  19. 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

  20. 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

  1. Tritium handling and processing experience at TSTA

    International Nuclear Information System (INIS)

    Anderson, J.L.; Okuno, K.

    1994-01-01

    In 1987, the Japan Atomic Energy Research Institute (JAERI) and the US Department of Energy (DOE) signed a collaborative agreement (Annex IV) for the joint funding and operation of the Tritium Systems Test Assembly (TSTA) at the Los Alamos National Laboratory (LANL) for a five year period ending June, 1992. After this initial five year collaboration, the Annex IV agreement was extended for another two year period ending June, 1994. During the first five years, a number of the integrated process loop tests of TSTA were conducted, as well as off-line testing of TSTA subsystems. During integrated loop testing the vacuum system, fuel cleanup systems, isotope separation system, transfer pumping system and gas analysis system, are interconnected and tested using 100 g-inventories of tritium to demonstrate steady-state operation of a tritium fuel processing cycle for a fusion reactor. These tests have resulted in a number of significant accomplishments and an experience data base on research, development and operation of the fuel processing system. One of the most significant accomplishments during the initial five year period was the continuous operation of the fuel processing loop for 25 days. During this 25-day extended operation, both the JAERI fuel cleanup system (J-FCU) and the original TSTA fuel cleanup system (FCU) were operated under similar conditions of flow, pressure, and impurity content of the DT gas. Both fuel cleanup systems were demonstrated to provide adequate impurity removal for plasma exhaust gas processing. The isotope separation system was operated continuously, producing pure tritium while rejecting protium as an impurity

  2. Tritium Facilities Modernization and Consolidation Project Process Waste Assessment (Project S-7726)

    Energy Technology Data Exchange (ETDEWEB)

    Hsu, R.H. [Westinghouse Savannah River Company, AIKEN, SC (United States); Oji, L.N.

    1997-11-14

    Under the Tritium Facility Modernization {ampersand} Consolidation (TFM{ampersand}C) Project (S-7726) at the Savannah River Site (SS), all tritium processing operations in Building 232-H, with the exception of extraction and obsolete/abandoned systems, will be reestablished in Building 233-H. These operations include hydrogen isotopic separation, loading and unloading of tritium shipping and storage containers, tritium recovery from zeolite beds, and stripping of nitrogen flush gas to remove tritium prior to stack discharge. The scope of the TFM{ampersand}C Project also provides for a new replacement R&D tritium test manifold in 233-H, upgrading of the 233- H Purge Stripper and 233-H/234-H building HVAC, a new 234-H motor control center equipment building and relocating 232-H Materials Test Facility metallurgical laboratories (met labs), flow tester and life storage program environment chambers to 234-H.

  3. Tritium Facilities Modernization and Consolidation Project Process Waste Assessment (Project S-7726)

    International Nuclear Information System (INIS)

    Hsu, R.H.; Oji, L.N.

    1997-01-01

    Under the Tritium Facility Modernization ampersand Consolidation (TFM ampersand C) Project (S-7726) at the Savannah River Site (SS), all tritium processing operations in Building 232-H, with the exception of extraction and obsolete/abandoned systems, will be reestablished in Building 233-H. These operations include hydrogen isotopic separation, loading and unloading of tritium shipping and storage containers, tritium recovery from zeolite beds, and stripping of nitrogen flush gas to remove tritium prior to stack discharge. The scope of the TFM ampersand C Project also provides for a new replacement R ampersand D tritium test manifold in 233-H, upgrading of the 233- H Purge Stripper and 233-H/234-H building HVAC, a new 234-H motor control center equipment building and relocating 232-H Materials Test Facility metallurgical laboratories (met labs), flow tester and life storage program environment chambers to 234-H

  4. Method and plant to remote tritium from the cooling water of a nuclear reactor

    International Nuclear Information System (INIS)

    O'Brien, C.J.

    1976-01-01

    A method is proposed for the extraction of tritium from the cooling water of a nuclear reactor, based on the principle of concentrating the tritium by a multi-stage transfer process. The cooling water is brought into contact in each stage with basic, labile, hydrogen-containing material with high pH value, whereby the tritium is transfered into an intermediate solid product and can be separated off. The technical details of the plant are described. Cellulose materials, such as cotton and wood as well as protein-containing material, such as muscle tissue are mentioned as examples of materials with a high affinity to tritium, greater than the affinity of water to tritium. They extract tritium from the cooling water. (HK) [de

  5. 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

  6. 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

  7. Tritium sorption by cement and subsequent release

    International Nuclear Information System (INIS)

    Ono, F.; Tanaka, S.; Yamawaki, M.

    1994-01-01

    In a fusion reactor or tritium handling facilities, contamination of concrete by tritium and subsequent release from it to the reactor or experimental rooms is a matter of problem for safety control of tritium and management of operational environment. In order to evaluate these tritium behavior, interaction of tritiated water with concrete or cement should be clarified. In the present study, HTO sorption and subsequent release from cement were studied by combining various experimental methods. From the basic studies on tritium-cement interactions, it has become possible to evaluate tritium uptake by cement or concrete and subsequent tritium release behavior as well as tritium removing methods from them

  8. TSTA loop operation with 100 grams-level of tritium

    International Nuclear Information System (INIS)

    Yoshida, Hiroshi; Hirata, Shingo; Naito, Taisei

    1988-10-01

    The first loop operation tests of Tritium Systems Test Assembly (TSTA) with 100 grams-level of tritium were carried out at Los Alamos National Laboratory(LANL) on June and July, 1987. The tests were one of the milestones for TSTA goal scheduled in June, 1987 through June, 1988. The objectives were (i) to operate TSTA process loop composed of tritium supply system, fuel gas purification system, hydrogen isotope separation system, etc, (ii) to demonstrate TSTA safety subsystems such as secondary containment system, tritium waste treatment system and tritium monitoring system, and (iii) to accumulate handling experience of a large amount of tritium. This report describes the plan and procedures of the milestone run done in June and the summary results especially on the safety aspects. Analysis of the emergency shutdown of the process loop, which happened in the June run, is also reported. A brief description of the process and safety subsystems as well as the summary of the TSTA safety analysis report is included. (author)

  9. 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

  10. Tritium recovery from fusion blankets using solid lithium compounds. I. Design and minimization of tritium inventory

    International Nuclear Information System (INIS)

    Powell, J.R.

    1975-01-01

    Tritium blanket inventories of 100 curies/MW(e) are readily achievable, and inventories as low as 10 curies/MW(e) are possible for blankets with small lithium compound particulates (less than or equal to 50μ) at T greater than or equal to 800 0 C. Of the three release modes [A - to the main coolant (e.g., He) stream; B - to a separate processing circuit; and C - to the plasma region], mode A appears optimum for blankets using gas-cooled metallic structures (e.g., Al, stainless), while mode C appears optimum for high temperature refractory (e.g., C, SiC) structures. The greater structural complexity of mode B makes it less attractive than modes A and C. No recovery method is required for mode C release. With mode A release, tritium inventory in the coolant circuits ranges from 1 to 10 curies/MW(e), depending on processing parameters. Tritium leak rates to the environment during normal operation can be kept to less than or equal to 10 -3 curies/MW(e) per day with low permeability barriers. In general, a mixture of T 2 and T 2 O is present in the coolant stream. Three methods of tritium recovery are examined: (1) Conversion to T 2 followed by absorption in a metal hydride bed. (2) Conversion to T 2 followed by condensation at approximately 6 0 K. (3) Conversion to T 2 O followed by condensation at approximately 100 0 K

  11. 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

  12. Tritium transport and control in the FED

    International Nuclear Information System (INIS)

    Rogers, M.L.

    1981-01-01

    The tritium systems for the FED have three primary purposes. The first is to provide tritium and deuterium fuel for the reactor. This fuel can be new tritium or deuterium delivered to the plant site, or recycled DT from the reactor that must be processed before it can be recycled. The second purpose of the FED tritium systems is to provide state-of-the-art tritium handling to limit worker radiation exposure and to minimize tritium losses to the environment. The final major objective of the FED tritium systems is to provide an integrated system test of the tritium handling technology necessary to support the fusion reactor program. Every effort is being made to incorporate available information from the Tritium System Test Assembly (TSTA) at Los Alamos National Laboratory, the Tokamak Fusion Test Reactor (TFTR) tritium systems, and the tritium handling information generated within DOE for the past 20 years

  13. Ontario Hydro diversifies into tritium

    International Nuclear Information System (INIS)

    Anon.

    1983-01-01

    A report is given on a plant which is to be built at the Darlington Candu reactor site in Canada for the extraction of tritium from heavy water. As tritium is used as a fuel in fusion research the market for it is expected to grow. The design of the system is outlined with the help of a flow diagram. (U.K.)

  14. Tritium containment in fusion facilities

    International Nuclear Information System (INIS)

    Anderson, J.L.

    1978-01-01

    The key environmental control systems that have been identified and are being developed are listed. A brief description of each of the following systems is given: primary process materials, permeation barriers, secondary containment, tritium waste treatment, emergency tritium cleanup, maintenance procedures, and tertiary containment

  15. Tritium accountancy in fusion systems

    Energy Technology Data Exchange (ETDEWEB)

    Klein, J.E.; Clark, E.A.; Harvel, C.D.; Farmer, D.A.; Tovo, L.L.; Poore, A.S. [Savannah River National Laboratory, Aiken, SC (United States); Moore, M.L. [Savannah River Nuclear Solutions, Aiken, SC (United States)

    2015-03-15

    The US Department of Energy (DOE) has clearly defined requirements for nuclear material control and accountability (MCA) of tritium whereas the International Atomic Energy Agency (IAEA) does not since tritium is not a fissile material. MCA requirements are expected for tritium fusion machines and will be dictated by the host country or regulatory body where the machine is operated. Material Balance Areas (MBA) are defined to aid in the tracking and reporting of nuclear material movements and inventories. Material sub-accounts (MSA) are established along with key measurement points (KMP) to further subdivide a MBA to localize and minimize uncertainties in the inventory difference (ID) calculations for tritium accountancy. Fusion systems try to minimize tritium inventory which may require continuous movement of material through the MSA. The ability of making meaningful measurements of these material transfers is described in terms of establishing the MSA structure to perform and reconcile ID calculations. For fusion machines, changes to the traditional ID equation will be discussed which includes breeding, burn-up, and retention of tritium in the fusion device. The concept of 'net' tritium quantities consumed or lost in fusion devices is described in terms of inventory taking strategies and how it is used to track the accumulation of tritium in components or fusion machines. (authors)

  16. 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.)

  17. 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

  18. Effective tritium processing using polyimide films

    International Nuclear Information System (INIS)

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

    1998-01-01

    Applying a gas separation membrane module of polyimide hollow fiber films, a new tritium removal system has been studied and designed to develop a more compact and cost-effective system than the conventional type of catalytic reactors and molecular sieves dryers. The recent investigations are focused on the development of a more effective membrane module, specifically, an increase in the processing capacity for a unit module. One idea is to purge the permeated side of the module by using a small part of the bleed flow as a counter-current flow. Another idea is to apply a new polyimide membrane module (Φ 0.1 x 1.8 m) with 5 times larger permeability of N 2 (0.24 std. m 3 h -1 atm -1 ) than the original one, though the selectivity (permeability ratio of H 2 /N 2 : 80) is reduced by about a half. The results show that the purging effect improves the module capacity to be 3 times larger and the new membrane has almost 5 times larger capacity under reasonable operation conditions with the same tritium decontamination ability. The total capacity of a unit module is being improved by more than 10 times. Using the recent results, a case design of the membrane detritiation system is discussed for an application to the ITER scale tritium facility. (orig.)

  19. Tritium metabolism in rat tissues

    International Nuclear Information System (INIS)

    Takeda, H.

    1982-01-01

    As part of a series of studies designed to evaluate the relative radiotoxicity of various tritiated compounds, metabolism of tritium in rat tissues was studied after administration of tritiated water, leucine, thymidine, and glucose. The distribution and retention of tritium varied widely, depending on the chemical compound administered. Tritium introduced as tritiated water behaved essentially as body water and became uniformly distributed among the tissues. However, tritium administered as organic compounds resulted in relatively high incorporation into tissue constituents other than water, and its distribution differed among the various tissues. Moreover, the excretion rate of tritium from tissues was slower for tritiated organic compounds than for tritiated water. Administrationof tritiated organic compounds results in higher radiation doses to the tissues than does administration of tritiated water. Among the tritiated compounds examined, for equal radioactivity administered, leucine gave the highest radiation dose, followed in turn by thymidine, glucose, and water. (author)

  20. Tritium behaviour in higher plants

    International Nuclear Information System (INIS)

    Guenot, J.

    1984-05-01

    Vine grapes and potato seedlings have been exposed in situ to tritiated water vapor and 14 C labeled carbon dioxide. Leaves sampling was done during and after the exposition. Measurements allowed to distinguish the three forms of tritium in leaves, i.e. tissue free water tritium (TFWT) and organically bound tritium (OBT), in exchangeable position or not. The results lead to a description of the dynamical behaviour of tritium between these three compartments. It has been shown that 20% of organically bound hydrogen is readily exchangeable thus being in permanent isotopic equilibium with tissue free water. Moreover, the activity of nonexchangeable OBT appears to be strongly related to the organic 14 C, which shows that photosynthesis is responsible of tritium incorporation in organic nonexchangeable position, and occurs with a 20% discrimination in favor of protium. In contrast with the other two compartments, this fixation is almost irreversible, which is a fact of importance from a radiological point of view [fr

  1. Tritium practices past and present

    International Nuclear Information System (INIS)

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

    1980-01-01

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

  2. 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

  3. TRICYCLE: a new mathematical model for tritium at the global scale

    International Nuclear Information System (INIS)

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

    1987-01-01

    TRICYCLE (for TRItium CYCLE) is a new linear dynamic compartment model that has been successful in reproducing environmental time-series data that show levels of tritium from nuclear weapons testing. Based on the global hydrologic cycle and other geophysical data, TRICYCLE includes (1) separate stratosphere compartments for the northern and southern hemispheres, (2) disaggregation of the troposphere and ocean surface waters into eight latitude zones each, (3) consideration of the different concentrations of tritium in atmospheric water vapor over land and over the ocean (the concentration over land exceeds that over the ocean by a factor of 3-4), and (4) a box-diffusion model for vertical transport in the ocean. The authors have used the model to simulate tritium in precipitation, ocean surface waters, and surface fresh waters (rivers and lakes). When they assume that 50% of the tritium from atmospheric weapons testing was injected directly into the northern stratosphere, the model gives good representations of tritium in the ocean surface waters and the rivers and lakes of the northern hemisphere; moreover, it estimates reasonable approximations to time-series measurements of tritium in marine precipitation taken at specific latitudes; and over the full range of latitudes, its representation of the high-to-low latitude gradient of tritium in marine precipitation is remarkable. Apart from their intrinsic geophysical interest, such models are useful in assessing the collective radiation dose to populations from tritium that is reeased at a particular latitude

  4. Tritium interactions of potential importance to fusion reactor systems: technology requirements

    International Nuclear Information System (INIS)

    Wilkes, W.R.

    1976-01-01

    The tritium technology requirements created by the controlled thermonuclear research program to develop a demonstration fusion power reactor by the year 2000 are reviewed. It is found that the majority of the technological advances which are needed to ensure adequate tritium containment in a tritium breeding power reactor need to be demonstrated on a pilot scale by approximately 1983, so that they may be incorporated into EPR-II, the second of two planned experimental power reactors. The most important advances include development of containment materials with permeabilities to tritium well below measured values for stainless steel; large scale, low inventory deuterium-tritium separation systems; and improved monitoring and assay systems. There are less critical requirements for information about the effects of tritium and helium on the mechanical properties of materials, the effects of tritium on biological systems, and data on physical and chemical properties of tritium. Substantial progress needs to be made on these problems early enough to permit possible solutions to be tested on EPR-I. In addition, major improvements in tritium handling equipment are required for EPR-I. Those technological problems for which solutions have not yet been demonstrated by EPR-II must be solved by 1989 if they are to be assured successful application in the demonstration reactor

  5. A system dynamics model for stock and flow of tritium in fusion power plant

    Energy Technology Data Exchange (ETDEWEB)

    Kasada, Ryuta, E-mail: r-kasada@iae.kyoto-u.ac.jp [Institute of Advanced Energy, Kyoto University, Gokasho, Uji, Kyoto 611-0011 (Japan); Kwon, Saerom [Institute of Advanced Energy, Kyoto University, Gokasho, Uji, Kyoto 611-0011 (Japan); Japan Atomic Energy Agency, Tokai-mura, Naka-gun, Ibaraki-ken 319-1195 (Japan); Konishi, Satoshi [Institute of Advanced Energy, Kyoto University, Gokasho, Uji, Kyoto 611-0011 (Japan); Sakamoto, Yoshiteru; Yamanishi, Toshihiko; Tobita, Kenji [Japan Atomic Energy Agency, Rokkasho-mura, Kamikita-gun, Aomori-ken 039-3212 (Japan)

    2015-10-15

    Highlights: • System dynamics model of tritium fuel cycle was developed for analyzing stock and flow of tritium in fusion power plants. • Sensitivity of tritium build-up to breeding ratio parameters has been assessed to two plant concepts having 3 GW and 1.5 GW fusion power. • D-D start-up absolutely without initial loading of tritium is possible for both of the 3 GW and 1.5 GW fusion power plant concepts. • Excess stock of tritium is generated by the steady state operation with the value of tritium breeding ratio over unity. - Abstract: In order to analyze self-efficiency of tritium fuel cycle (TFC) and share the systems thinking of TFC among researchers and engineers in the vast area of fusion reactor technology, we develop a system dynamics (SD) TFC model using a commercial software STELLA. The SD-TFC model is illustrated as a pipe diagram which consists of tritium stocks, such as plasma, fuel clean up, isotope separation, fueling with storage and blanket, and pipes connecting among them. By using this model, we survey a possibility of D-D start-up without initial loading of tritium on two kinds of fusion plant having different plasma parameters. The D-D start-up scenario can reduce the necessity of initial loading of tritium through the production in plasma by D-D reaction and in breeding blanket by D-D neutron. The model is also used for considering operation scenario to avoid excess stock of tritium which must be produced at tritium breeding ratio over unity.

  6. Measurement of tritium in tissue free water of pine needles

    International Nuclear Information System (INIS)

    Zheng Xiaomin; Wu Zongmei

    1993-01-01

    Tissue Free Water (TFW) of pine needles is separated out through azeotropic distillation of pine needles and toluene. Recovery ratio of TFW is 90%. Tritium activity in the needles is 1.8 Bq/L(H 2 O), which is of the same level with tritiated water vapour (HTO) in atmosphere during the corresponding period

  7. Torus evacuation and tritium handling on NET

    International Nuclear Information System (INIS)

    Dinner, P.; Chazalon, M.; Iseli, M.

    1986-08-01

    The use of tritium as a fuel affects the design of many systems, as well as requiring several new systems not needed on non DT-burning Tokamaks. This paper summarizes: major tritium process interconnections, tritium flows and inventories; primary requirements, preferred design alternatives, and related development issues; design philosophy for tritium and primary vacuum systems. 14 refs

  8. Contribution to the tritium continental effect

    International Nuclear Information System (INIS)

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

    1987-01-01

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

  9. Contribution to the tritium continental effect

    International Nuclear Information System (INIS)

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

    1987-01-01

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

  10. Overview of the tritium system of Ignitor

    International Nuclear Information System (INIS)

    Rizzello, C.; Tosti, S.

    2008-01-01

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

  11. Mixed deuterium-tritium neutral beam injection

    International Nuclear Information System (INIS)

    Ruby, L.; Lewis, M.S.

    1989-01-01

    An alternative mixed beam neutral beam injector (MNBI) for fusion reactors is proposed that eliminates the conventional isotope separation system (ISS) in the fuel cycle. The principal advantage of the alternative system is a capital and operating cost savings in the fuel cycle, as the ISS employs cryogenic distillation at liquid-hydrogen temperatures to effect a separation of hydrogen isotopes and to eliminate a buildup of normal hydrogen in the recycled fuel. Possible additional advantages of the alternative method involve an improvement in overall safety and a reduction of the amount of tritium in the fuel cycle. The alternative heating system uses an electromagnetic separation in the MNBI to limit the buildup of normal hydrogen. Calculations indicate that an MNBI can be reasonably optimized in the case of an upgraded injection system for the Tokamak Fusion Test Reactor

  12. Tritium, biography of an element

    International Nuclear Information System (INIS)

    Keller, C.

    1980-01-01

    Tritium is the lightest radioactive atom, an isotope of hydrogen. In science it has many uses, particularly for marking organic molecules in order to find out about biochemical and medical processes. But also the traces of tritium contained in rain or sea water are used for investigations; they range from establishing the vintage of old wines to ascertaining sea water mixtures. Tritium will become important in large-scale technology if it should become possible to construct fusion reactors, since it is one of the fuels. (orig.) [de

  13. Tritium monitor for fusion reactors

    Energy Technology Data Exchange (ETDEWEB)

    Jalbert, R.A.

    1982-08-01

    This report describes the design, operation, and performance of a flow-through ion-chamber instrument designed to measure tritium concentrations in air containing /sup 13/N, /sup 16/N, and /sup 41/Ar produced by neutrons generated by D-T fusion devices. The instrument employs a chamber assembly consisting of two coaxial ionization chambers. The inner chamber is the flow-through measuring chamber and the outer chamber is used for current subtraction. A thin wall common to both chambers is opaque to the tritium betas. Currents produced in the two chambers by higher energy radiation are automatically subtracted, leaving only the current due to tritium.

  14. The organically bound tritium: an analyst vision

    International Nuclear Information System (INIS)

    Ansoborlo, E.; Baglan, N.

    2009-01-01

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

  15. Tritium monitoring at the Sandia Tritium Research Laboratory

    International Nuclear Information System (INIS)

    Devlin, T.K.

    1978-10-01

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

  16. 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

  17. Thought experiment with tritium

    International Nuclear Information System (INIS)

    Anderson, H.F.; Everhart, J.L.; Hobrock, D.L.; Seabaugh, P.W.

    1995-01-01

    An experiment is proposed in which a minimum of thirty (30) grams of tritium is packaged as lithium tritide in a steel container weighing several kilograms. After decontamination of the outside surface, calorimetry measurements would be made, and the unit would be weighed very accurately. After several decades, the calorimeter and weight measurements would be repeated. If the weight measurements could be made with the required accuracy, it would be possible to correlate the observed change in mass with the total energy emitted (calculated from the mean energy measured by calorimetry) over the time interval. If successful, this experiment would, in the opinion of the authors, be the first laboratory experiment to directly verify the equivalency of mass and energy. 4 refs., 2 figs., 3 tabs

  18. Tritium containment of controlled thermonuclear fusion reactor

    International Nuclear Information System (INIS)

    Tanaka, Yoshihisa; Tsukumo, Kiyohiko; Suzuki, Tatsushi

    1979-01-01

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

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

    International Nuclear Information System (INIS)

    Jalbert, R.A.

    1982-07-01

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

  20. Measurement of organically bound tritium in urine and feces

    International Nuclear Information System (INIS)

    Trivedi, A.; Duong, T.; Leon, J.W.; Linauskas, S.H.

    1993-11-01

    A bioassay method was developed for directly measuring organically bound tritium (OBT) in urine and feces. Samples first undergo low-temperature distillation and vacuum separation to isolate tritiated water (HTO) and exchangeable tritium. This is followed by converting the non-exchangeable tritium (i.e., OBT) into HTO through oxygen combustion. The method was investigated to: optimise the sample preparation procedures; establish OBT recovery (64% ± 7% for urine and 71% ± 8% for feces); and, determine the detection limit for OBT in urine (0.3 Bq · g -1 ) and feces (5 Bq · g -1 ). The method was evaluated for error sources that are associated with the exchange between HTO and OBT. It is concluded that this bioassay method can reliably measure OBT in urine and feces within the range of ± 10%

  1. In vitro study of proteins surface activity by tritium probe

    International Nuclear Information System (INIS)

    Chernysheva, M.G.; Badun, G.A.

    2010-01-01

    A new technique for in vitro studies of biomacromolecules interactions, their adsorption at aqueous/organic liquid interfaces and distribution in the bulk of liquid/liquid systems was developed. The method includes (1) tritium labeling of biomolecules by tritium thermal activation method and (2) scintillation phase step with organic phase, which can be concerned as a model of cellular membrane. Two globular proteins lysozyme and human serum albumin tested. We have determined the conditions of tritium labeling when labeled by-products can be easy separated by means of dialysis and size-exclusion chromatography. Scintillation phase experiments were conducted for three types of organic liquids. Thus, the influences of the nature of organic phase on proteins adsorption and its distribution in the bulk of aqueous/organic liquid system were determined. It was found that proteins possess high surface activity at aqueous/organic liquid interface. Furthermore, values of hydrophobicity of globular proteins were found by the experiment. (author)

  2. Tritium transport around nuclear facilities

    International Nuclear Information System (INIS)

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

    1981-01-01

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

  3. TFTR tritium inventory accountability system

    International Nuclear Information System (INIS)

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

    1995-01-01

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

  4. Tritium management for fusion reactors

    International Nuclear Information System (INIS)

    Rouyer, J.L.; Djerassi, H.

    1985-01-01

    To determine a waste management strategy, one has to identify first the wastes (quantities, activities, etc.), then to define options, and to compare these options by appropriate criteria and evaluations. Two European Associations are working together, i.e., Studsvik and CEA, on waste treatment and tritium problems. A contribution to fusion specific tritiated waste management strategy is presented. It is demonstrated that the best strategy is to retain tritium (outgas and recover, or immobilize it) so that residual tritium releases are kept to a minimum. For that, wastes are identified, actual regulations are described and judged inadequate without amendments for fusion problems. Appropriate criteria are defined. Options for treatment and disposal of tritiated wastes are proposed and evaluated. A tritium recovery solution is described

  5. Radiotoxicity of tritium in mammals

    International Nuclear Information System (INIS)

    Silini, G.; Metalli, P.; Vulpis, G.

    1972-12-01

    Basic data relative to tritium, its physicochemical behaviour in environment, its major sources of contamination and its metabolism through the mammalian organisms are reviewed. After considering the radiotoxicity of tritium particularly at the cellular and whole-body level the conclusion is drawn that the major uncertainties regard the fraction of tritium incorporated into the nuclei of some tissues. This fraction is eliminated very slowly and is capable of modifying the genetic structures of the nucleus. A more refined analysis of radiobiological phenomena and a better knowledge of the dose effect relationship should permit the extrapolation of the data to the low doses of tritium contamination. This extrapolation is of great interest in the field of public health for the elaboration of the relevant radioprotection standards

  6. Tritium transport around nuclear faciliteis

    International Nuclear Information System (INIS)

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

    1982-01-01

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

  7. Tritium in fusion reactor components

    International Nuclear Information System (INIS)

    Watson, J.S.; Fisher, P.W.; Talbot, J.B.

    1980-01-01

    When tritium is used in a fusion energy experiment or reactor, several implications affect and usually restrict the design and operation of the system and involve questions of containment, inventory, and radiation damage. Containment is expected to be particularly important both for high-temperature components and for those components that are prone to require frequent maintenance. Inventory is currently of major significance in cases where safety and environmental considerations limit the experiments to very low levels of tritium. Fewer inventory restrictions are expected as fusion experiments are placed in more-remote locations and as the fusion community gains experience with the use of tritium. However, the advent of power-producing experiments with high-duty cycle will again lead to serious difficulties based principally on tritium availability; cyclic operations with significant regeneration times are the principal problems

  8. Parameter study on Japanese proposal of ITER hydrogen isotope separation system

    International Nuclear Information System (INIS)

    Yoshida, Hiroshi; Enoeda, Mikio; Tanaka, Shigeru; Ohokawa, Yoshinao; Ohara, Atsushi; Nagakura, Masaaki; Naito, Taisei; Nagashima, Kazuhiro.

    1991-01-01

    As part of Japanese design contribution in the ITER activity, conceptual design of an entire ITER tritium system and their safety analysis have been carried out through the three-year period since 1988. The tritium system includes the following subsystems; - Fuelling (gas puffing and pellet injection) subsystem, - Torus vacuum pumping subsystem, - Plasma exhaust gas purification subsystem, - Hydrogen isotope separation subsystem, - NBI gas processing subsystem, - Blanket tritium recovery subsystem, - Tritiated water processing subsystem, - Tritium safety subsystem. Hydrogen isotope separation system is a key subsystem in the ITER tritium system because it is connected to all above subsystems. This report describes an analytical study on the Japanese concept of hydrogen isotope separation system. (author)

  9. The human body retention time of environmental organically bound tritium

    Energy Technology Data Exchange (ETDEWEB)

    Hunt, John; Bailey, Trevor [Centre for Environment, Fisheries and Aquaculture Science, Pakefield Road, Lowestoft, Suffolk NR33 0HT (United Kingdom); Reese, Allan [Centre for Environment, Fisheries and Aquaculture Science, The Nothe, Barrack Road, Weymouth, Dorset DT4 8UB (United Kingdom)], E-mail: john.hunt@cefas.co.uk

    2009-03-15

    Tritium in the UK environment causes low radiation doses to the public, but uncertainty exists in the dose coefficient for the organically bound component of tritium (OBT). This can affect the assessment of effective doses to representative persons. Contributing to that uncertainty is poor knowledge of the body retention time of OBT and how this varies for different OBT compounds in food. This study was undertaken to measure the retention time of tritium by volunteers after eating sole from Cardiff Bay, which may contain OBT from discharges from the GE Healthcare Ltd plant. Five volunteers provided samples of excreta over periods up to 150 days after intake. The results, which are presented in raw form to allow independent analysis, suggest retention of total tritium with body half-times ranging from 4 to 11 days, with no evidence (subject to experimental noise) of a significant contribution due to retention with a longer half-time. This range covers the half-time of 10 days used by the ICRP for tritiated water. The short timescale could be due to rapid hydrolysis in body tissues of the particular form of OBT used in this study. Implications for the dose coefficient for OBT are that the use of the ICRP value of 4.2 x 10{sup -11} Sv Bq{sup -1} may be cautious in this specific situation. These observations on dose coefficients are separate from any implications of recent discussion on whether the tritium radiation weighting factor should be increased from 1 to 2.

  10. 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

  11. Tritium control and accountability instructions

    International Nuclear Information System (INIS)

    Wall, W.R.; Cruz, S.L.

    1985-08-01

    This instruction describes the tritium accountability procedures practiced by the Tritium Research Laboratory, at Sandia National Laboratories, Livermore. The accountability procedures are based upon the Sandia National Laboratories, Livermore, Nuclear Materials Operations Manual, SAND83-8036. The Nuclear Materials Operations Manual describes accountability techniques which are in compliance with the Department of Energy 5630 series Orders, Code of Federal Regulations, and Sandia National Laboratories Instructions

  12. Tritium pellet injector for TFTR

    International Nuclear Information System (INIS)

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

    1992-01-01

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

  13. Tritium control and accountability instructions

    International Nuclear Information System (INIS)

    Wall, W.R.

    1981-03-01

    This instruction describes the tritium accountability procedures practiced by the Tritium Research Laboratory, Building 968 at Sandia National Laboratories, Livermore. The accountability procedures are based upon the Sandia National Laboratories, Livermore, Nuclear Materials Operations Manual, SAND78-8018. The Nuclear Materials Operations Manual describes accountability techniques which are in compliance with the Department of Energy Manual, Code of Federal Regulations, and Sandia National Laboratories Instructions

  14. 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)

  15. Tritium research activities in Korea

    Energy Technology Data Exchange (ETDEWEB)

    Jung, Ki Jung, E-mail: kjjung@nfri.re.kr [National Fusion Research Institute, Yusung-gu, Daejeon 305-333 (Korea, Republic of); Yun, Sei-Hun, E-mail: shyun@nfri.re.kr [National Fusion Research Institute, Yusung-gu, Daejeon 305-333 (Korea, Republic of); Chang, Min Ho; Kang, Hyun-Goo; Chung, Dongyou; Cho, Seungyon; Lee, Hyeon Gon [National Fusion Research Institute, Yusung-gu, Daejeon 305-333 (Korea, Republic of); Chung, Hongsuk; Choi, Woo-Seok [Korea Atomic Energy Research Institute, Yusung-gu, Daejeon 305-353 (Korea, Republic of); Song, Kyu-Min; Moon, Chang-Bae [Korea Hydro & Nuclear Power Central Research Institute, Yusung-gu, Daejeon 305-343 (Korea, Republic of); Lee, Euy Soo [Dongguk University, Jung-gu, Seoul, 100-715 (Korea, Republic of); Cho, Jungho; Kim, Dong-Sun [Kongju National University, Cheonan, Chungnam, 330-717 (Korea, Republic of); Moon, Hung-Man [Daesung Industrial Gases Co., Ltd., Danwon-gu, Ansan-si, Gyeonggi-do, 425-090 (Korea, Republic of); Noh, Seung Jeong [Dankook University, Suji-gu, Yongin-si, Gyeonggi-do, 448-701 (Korea, Republic of); Ju, Hyunchul [Inha University, Nam-gu, Incheon, 402-751 (Korea, Republic of); Hong, Tae-Whan [Korea National University of Transportation, Chungju, Chungbuk, 380-702 (Korea, Republic of)

    2016-12-15

    Highlights: • NFRI, KAERI and KHNP CRI are major leading group for the ITER tritium SDS design; studying engineering, simulation of hydride bed, risk analysis (on safety, HAZOP), basic study, control logic & sequential operation, and others. KHNP has WTRF which gives favorable experiences for collaboration researchers. • Supplementary research partners: Five Universities (Dongguk University and POSTECH, Inha University, Dankook University, Korea National Transport University, and Kongju National University) and one industrial company (Daesung Industrial Gases Co., Ltd.); studying on basic and engineering, programming & simulation on the various topics for ITER tritium SDS, TEP, ISS, ADS, and etc. - Abstract: Major progress in tritium research in the Republic of Korea began when Korea became responsible for ITER tritium Storage and Delivery System (SDS) procurement package which is part of the ITER Fuel Cycle. To deliver the tritium SDS package, a variety of research institutes, universities and industry have respectively taken roles and responsibilities in developing technologies that have led to significant progress. This paper presents the current work and status of tritium related technological research and development (R&D) in Korea and introduces future R&D plans in the area of fuel cycle systems for fusion power generation.

  16. 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.)

  17. A new combination of membranes and membrane reactors for improved tritium management in breeder blanket of fusion machines

    International Nuclear Information System (INIS)

    Demange, D.; Staemmler, S.; Kind, M.

    2011-01-01

    Tritium used as fuel in future fusion machines will be produced within the breeder blanket. The tritium extraction system recovers the tritium to be routed into the inner-fuel cycle of the machine. Accurate and precise tritium accountancy between both systems is mandatory to ensure a reliable operation. Handling in the blanket huge helium flow rates containing tritium as traces in molecular and oxide forms is challenging both for the process and the accountancy. Alternative tritium processes based on combinations of membranes and membrane reactors are proposed to facilitate the tritium management. The PERMCAT process is based on counter-current isotope swamping in a palladium membrane reactor. It allows recovering tritium efficiently from any chemical species. It produces a pure hydrogen stream enriched in tritium of advantage for integration upstream of the accountancy stage. A pre-separation and pre-concentration stage using new zeolite membranes has been studied to optimize the whole process. Such a combination could improve the tritium processes and facilitate accountancy in DEMO.

  18. A study of organic binding of incorporated tritium by means of the organic components of human urine

    International Nuclear Information System (INIS)

    Szilagyi, M.

    1976-01-01

    The change in tritium activity of metabolytic fractions of urine of persons working in the production of tritium labelled compounds was studied. The radioactivity of the separated fractions was measured during a 20 day period. A carbamide fraction proved to be the most sensitive to incorporative cases owing to its organic component fractioned together with the carbamide. (K.A.)

  19. 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)

  20. Tritium problems in fusion reactor systems

    International Nuclear Information System (INIS)

    Hickman, R.G.

    1975-01-01

    A brief introduction is given to the role tritium will play in the development of fusion power. The biological and worldwide environmental behavior of tritium is reviewed. The tritium problems expected in fusion power reactors are outlined. A few thoughts on tritium permeation and recent results for tritium cleanup and CT 4 accumulation are presented. Problems involving the recovery of tritium from the breeding blanket in fusion power reactors are also considered, including the possible effect of impurities in lithium blankets and the use of lithium as a regenerable getter pump. (auth)

  1. 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.)

  2. Tritium fractionation in biological systems and in analytical procedures

    International Nuclear Information System (INIS)

    Kim, M.A.; Baumgaertner, F.

    1991-01-01

    The organically bound tritium (OBT) is evaluated in biological systems by measuring the tritium distribution ratio (R-value), i.e. tritium concentrations in organic substance to tissue water. The determination of the R-value is found to involve always isotope fractionation in applied analytical procedures and hence the evaluation of the true OBT-value in a given biological system appears more complicated than hitherto known in the literature. The present work concentrates on the tritium isotope fraction in the tissue water separation and on the resulting effects on the R-value. The analytical procedures examined are vacuum freeze drying under equilibrium and non-equilibrium conditions and azeotropic distillation. The vaporization isotope effects are determined separately in the phase transition of solid or liquid to gas in pure water systems as well as in real biological systems, e.g. maize plant. The results are systematically analysed and the influence of isotope effects on the R-value is rigorously quantified. (orig.)

  3. Turkey Point tritium. Progress report

    International Nuclear Information System (INIS)

    Ostlund, H.G.; Dorsey, H.G.

    1976-01-01

    In 1972-73 the Florida Power and Light Company (FPL) began operation of two nuclear reactors at Turkey Point on lower Biscayne Bay. One radioactive by-product resulting from the operation of the nuclear reactors, tritium, provides a unique opportunity to study transport and exchange processes on a local scale. Since the isotope in the form of water is not removed from the liquid effluent, it is discharged to the cooling canal system. By studying its residence time in the canal and the pathways by which it leaves the canals, knowledge of evaporative process, groundwater movement, and bay exchange with the ocean can be obtained. Preliminary results obtained from measurement of tritium levels, both in the canal system and in the surrounding environment are discussed. Waters in lower Biscayne Bay and Card and Barnes Sounds receive only a small portion of the total tritium produced by the nuclear plant. The dominating tritium loss most likely is through evaporation from the canals. The capability of measuring extremely low HTO levels allows the determination of the evaporation rate experimentally by measuring the tritium levels of air after having passed over the canals

  4. Tritium Management Loop Design Status

    Energy Technology Data Exchange (ETDEWEB)

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

    2017-12-01

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

  5. Transient behavior of enrichment of tritium water in adsorption-distillation column

    International Nuclear Information System (INIS)

    Fukada, Satoshi

    2006-01-01

    Enrichment of tritium in an adsorption-distillation column was experimentally investigated under the two processes of simple distillation and total-reflux distillation. Adsorption of water on silica-gel pellets enhanced the total isotope separation factor in the water distillation column. The transient behavior of tritium enrichment was analyzed using material balance equations of tritium and water in each cell with a height corresponding to HETP. The experimental transient behavior was well simulated by the material balance equations with additional assumptions on vapor and liquid flow rates regardless of the different processes of simple distillation and total-reflux distillation. (author)

  6. Tentative reference method for measurement of tritium in environmental waters. Environmental monitoring series

    International Nuclear Information System (INIS)

    1975-12-01

    A tentative reference method for the measurement of tritium in potable and nonpotable environmental water is described. Water samples are treated with sodium hydroxide and potassium permanganate and then a water fraction is separated from interferences by distillation. Two distillation procedures are described, a simple aqueous distillation for samples from potable water sources, and an aqueous-azeotropic-benzene distillation for nonpotable water sources. Alliquots of a designated distillate fraction are measured for tritium activity by liquid scintillation detection. Distillation recovery and counting efficiency factors are determined with tritium standards. Results are reported in picocuries per milliliter

  7. 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.)

  8. Tritium in the environment. Knowledge synthesis

    International Nuclear Information System (INIS)

    2009-01-01

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

  9. Recommended radiological controls for tritium operations

    International Nuclear Information System (INIS)

    Mansfield, G.

    1992-01-01

    This informal report presents recommendations for an adequate radiological protection program for tritium operations. Topics include hazards analysis, facility design, personnel protection equipment, training, operational procedures, radiation monitoring, to include surface and airborne tritium contamination, and program management

  10. Technologies for immobilization and disposal of tritium; Tecnologias para inmobilizacion y disposicion de tritio

    Energy Technology Data Exchange (ETDEWEB)

    Coppari, N R [Comision Nacional de Energia Atomica, San Martin (Argentina). Unidad de Actividad Reactores y Centrales Nucleares

    1997-12-31

    This study was done within a program one of whose objectives was to know the state of the technology development for tritium separation in the moderator circuit at HWR and to define the possible technologies to be applied to the Argentine nuclear power plants. Within this framework the strategies adopted by each country and the available technologies for a safe disposal of tritium, not only in its gaseous state tritium but also as tritiated water were analyzed. It is considered that if the selected separation method is such that the tritium is in its gaseous state, the hydride formation for long periods of immobilization should be studied. whereas if it were triated water immobilization should be studied to choose the technology between cementation and drying agents, in both cases the final disposal site will have to be selected. (author). 8 refs.

  11. Tritium in metals: Techniques of preparation

    International Nuclear Information System (INIS)

    Laesser, R.; Klatt, K.H.; Mecking, P.; Wenzl, H.

    1982-08-01

    In order to study the behavior of tritium in metals, an all metal apparatus has been built for the safe handling of 100 mg of tritium. Samples of palladium, vanadium, niobium, and tantalum were loaded with tritium, deuterium or hydrogen. Some details of the phase diagrams could be established by DTA and by measurement of the lattice parameters. The diffusion of tritium in V, Nb, and Ta was studied with the Gorsky-effect. (TWO)

  12. Tritium decontamination of machine components and walls

    International Nuclear Information System (INIS)

    Hircq, B.; Wong, K.Y.; Jalbert, R.A.; Shmayda, W.T.

    1991-01-01

    Tritium decontamination techniques for machine components and their application at tritium handling facilities are reviewed. These include commonly used methods such as vacuuming, purging, thermal desorption and isotopic exchange as well as less common methods such as chemical/electrochemical etching, plasma discharge cleaning, and destructive methods. Problems associated with tritium contamination of walls and use of protective coatings are reviewed. Tritium decontamination considerations at fusion facilities are discussed

  13. Gas chromatography at the Tritium Laboratory Karlsruhe

    International Nuclear Information System (INIS)

    Laesser, R.; Gruenhagen, S.

    2003-08-01

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

  14. Tritium calorimeter setup and operation

    CERN Document Server

    Rodgers, D E

    2002-01-01

    The LBNL tritium calorimeter is a stable instrument capable of measuring tritium with a sensitivity of 25 Ci. Measurement times range from 8-hr to 7-days depending on the thermal conductivity and mass of the material being measured. The instrument allows accurate tritium measurements without requiring that the sample be opened and subsampled, thus reducing personnel exposure and radioactive waste generation. The sensitivity limit is primarily due to response shifts caused by temperature fluctuation in the water bath. The fluctuations are most likely a combination of insufficient insulation from ambient air and precision limitations in the temperature controller. The sensitivity could probably be reduced to below 5 Ci if the following improvements were made: (1) Extend the external insulation to cover the entire bath and increase the top insulation. (2) Improve the seal between the air space above the bath and the outside air to reduce evaporation. This will limit the response drift as the water level drops. (...

  15. Polymeric media for tritium fixation

    International Nuclear Information System (INIS)

    Franz, J.A.; Burger, L.L.

    1975-01-01

    The synthesis and leach testing of several polymeric media for tritium fixation are presented. Tritiated bakelite, poly(acrylonitrile) and polystyrene successfully fixed tritium. Tritium leach rates at the tracer level appear to be negligible. Advantages and disadvantages of the processes are discussed, and further bench-scale investigations underway are reported. Rough cost estimates are presented for the different media and are compared with alternate approaches such as deep-well injection and long-term tank storage. Polymeric media costs are high compared to deep-well storage and are of the same order of magnitude per liter of water as for isotopic enrichment. With this limitation, polymeric media can be economically feasible only for highly concentrated tritiated wastes. It is recommended that the bakelite and polystyrene processes be examined on a larger scale to permit more accurate cost analysis and process design. (auth)

  16. Tritium processing using metal hydrides

    International Nuclear Information System (INIS)

    Mallett, M.W.

    1986-01-01

    E.I. duPont de Nemours and Company is commissioned by the US Department of Energy to operate the Savannah River Plant and Laboratory. The primary purpose of the plant is to produce radioactive materials for national defense. In keeping with current technology, new processes for the production of tritium are being developed. Three main objectives of this new technology are to ease the processing of, ease the storage of, and to reduce the operating costs of the tritium production facility. Research has indicated that the use of metal hydrides offers a viable solution towards satisfying these objectives. The Hydrogen and Fuels Technology Division has the responsibility to conduct research in support of the tritium production process. Metal hydride technology and its use in the storage and transportation of hydrogen will be reviewed

  17. Implanted-tritium permeation experiments

    International Nuclear Information System (INIS)

    Longhurst, G.R.; Holland, D.F.; Casper, L.A.; Hsu, P.Y.; Miller, L.G.; Schmunk, R.E.; Watts, K.D.; Wilson, C.J.; Kershner, C.J.; Rogers, M.L.

    1982-04-01

    In fusion reactors, charge exchange neutral atoms of tritium coming from the plasma will be implanted into the first wall and other interior structures. EG and G Idaho is conducting two experiments to determine the magnitude of permeation into the coolant streams and the retention of tritium in those structures. One experiment uses an ion gun to implant deuterium. The ion gun will permit measurements to be made for a variety of implantation energies and fluxes. The second experiment utilizes a fission reactor to generate a tritium implantation flux by the 3 He(n,p) 3 H reaction. This experiment will simulate the fusion reactor radiation environment. We also plan to verify a supporting analytical code development program, in progress, by these experiments

  18. 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)

  19. Tritium inventory prediction in a CANDU plant

    International Nuclear Information System (INIS)

    Song, M.J.; Son, S.H.; Jang, C.H.

    1995-01-01

    The flow of tritium in a CANDU nuclear power plant was modeled to predict tritium activity build-up. Predictions were generally in good agreement with field measurements for the period 1983--1994. Fractional contributions of coolant and moderator systems to the environmental tritium release were calculated by least square analysis using field data from the Wolsong plant. From the analysis, it was found that: (1) about 94% of tritiated heavy water loss came from the coolant system; (2) however, about 64% of environmental tritium release came from the moderator system. Predictions of environmental tritium release were also in good agreement with field data from a few other CANDU plants. The model was used to calculate future tritium build-up and environmental tritium release at Wolsong site, Korea, where one unit is operating and three more units are under construction. The model predicts the tritium inventory at Wolsong site to increase steadily until it reaches the maximum of 66.3 MCi in the year 2026. The model also predicts the tritium release rate to reach a maximum of 79 KCi/yr in the year 2012. To reduce the tritium inventory at Wolsong site, construction of a tritium removal facility (TRF) is under consideration. The maximum needed TRF capacity of 8.7 MCi/yr was calculated to maintain tritium concentration effectively in CANDU reactors

  20. 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

  1. Bioassay guideline 2: guidelines for tritium bioassay

    International Nuclear Information System (INIS)

    1983-01-01

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

  2. 10 CFR 30.55 - Tritium reports.

    Science.gov (United States)

    2010-01-01

    ... 10 Energy 1 2010-01-01 2010-01-01 false Tritium reports. 30.55 Section 30.55 Energy NUCLEAR..., Inspections, Tests, and Reports § 30.55 Tritium reports. (a)-(b) [Reserved] (c) Except as specified in paragraph (d) of this section, each licensee who is authorized to possess tritium shall report promptly to...

  3. Toxicity and dosimetry of tritium

    International Nuclear Information System (INIS)

    Myers, D.K.; Johnson, J.R.

    1991-01-01

    Tritium doses to the general public are very low (currently about 0.2 μSv per year). Radiation doses from tritium to members of the public living in the vicinity of a CANDU power station are higher but rarely exceed 20 μSv per year or 1% of normal exposures to radiation from all natural sources, but doses to some radiation workers can approach ten mSv per year. The relative biological effectiveness (RBE) of tritium beta rays varies appreciably depending upon the biological endpoint. Observed RBE values at low doses and low dose-rates are usually about 2 to 3 when tritium beta rays are compared to 60 Co gamma rays but are closer to 1 than to 2 when compared to 200 kVp X-rays. This conclusion is supported by microdosimetric considerations of the quality of tritium beta rays, 60 Co gamma rays and X-rays. Since X-rays have traditionally been accepted as reference radiation by the International Commission on Radiological Protection, it seems reasonable that the quality factor (Q) assigned to tritium beta rays should be close to one. Recommended procedures in Canada for estimation of effective dose equivalents from exposures to HTO and HT assume that Q = 1 and that body water represents 67% of the mass of soft tissue; they take into account conversions of HTO to appear to be reasonable for radiation protection purposes when the source of exposure is HTO or HT, but will not be adequate for exposures to other tritiated compounds. (modified author abstract) (137 refs., 11 figs., 12 tabs.)

  4. The INEL Tritium Research Facility

    International Nuclear Information System (INIS)

    Longhurst, G.R.

    1990-01-01

    The Tritium Research Facility (TRF) at the Idaho National Engineering Laboratory (INEL) is a small, multi-user facility dedicated to research into processes and phenomena associated with interaction of hydrogen isotopes with other materials. Focusing on bench-scale experiments, the main objectives include resolution of issues related to tritium safety in fusion reactors and the science and technology pertinent to some of those issues. In this report the TRF and many of its capabilities will be described. Work presently or recently underway there will be discussed, and the implications of that work to the development of fusion energy systems will be considered. (orig.)

  5. The INEL Tritium Research Facility

    Energy Technology Data Exchange (ETDEWEB)

    Longhurst, G.R. (Idaho National Engineering Lab., Idaho Falls (USA))

    1990-06-01

    The Tritium Research Facility (TRF) at the Idaho National Engineering Laboratory (INEL) is a small, multi-user facility dedicated to research into processes and phenomena associated with interaction of hydrogen isotopes with other materials. Focusing on bench-scale experiments, the main objectives include resolution of issues related to tritium safety in fusion reactors and the science and technology pertinent to some of those issues. In this report the TRF and many of its capabilities will be described. Work presently or recently underway there will be discussed, and the implications of that work to the development of fusion energy systems will be considered. (orig.).

  6. Tritium turnover in succulent plants

    International Nuclear Information System (INIS)

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

    1977-01-01

    Measurements of turnover rates for tissue free water tritium (TFWT) and tissue bound tritium (TBT) were carried out in three succulent plants, Opuntia sp., E. Trigona and E. Mili using tritiated water as tracer. The estimated half-times were 52, 57.5 and 80 days for TFWT and 212, 318 and 132 days for TBT in the stems of the above plants respectively. Opuntia sp. showed significant incorporation of TBT, 10% of TFWT on weight basis, while the other two plants showed lesser incorporation, 2-3% of TFWT. However, the leaves of E. Mili indicated the same level of fixation of TBT as the stem of Opuntia sp. (author)

  7. ITER task title - source term data, modelling, and analysis. ITER subtask no. S81TT05/5 (SEP 1-1). Global tritium source term analysis basis document. Subtask 1: operational tritium effluents and releases. Final report (1995 TASK)

    International Nuclear Information System (INIS)

    Kalyanam, K.M.

    1996-06-01

    This document represents the final report for the global tritium source term analysis task initiated in 1995. The report presents a room-by-room map/table at the subsystem level for the ITER tritium systems, identifying the major equipment, secondary containments, tritium release sources, duration/frequency of tritium releases and the release pathways. The chronic tritium releases during normal operation, as well as tritium releases due to routine maintenance of the Water Distillation Unit, Isotope Separation System and Primary and Secondary Heat Transport Systems, have been estimated for most of the subsystems, based on the IDR design, the Design Description Documents (April - Jun 1995 issues) and the design updates up to December 1995. The report also outlines the methodology and the key assumptions that are adopted in preparing the tritium release estimates. The design parameters for the ITER Basic Performance Phase (BPP) have been used in estimating the tritium releases shown in the room-by-room map/table. The tritium release calculations and the room-by-room map/table have been prepared in EXCEL, so that the estimates can be refined easily as the design evolves and more detailed information becomes available. (author). 23 refs., tabs

  8. 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)

  9. The tritium confinement and surface chemistry of plasma facing materials in controlled D-T fusion devices

    International Nuclear Information System (INIS)

    Wu, C.H.

    1987-01-01

    Tritium permeation through first walls, limiters or divertors subjected to energetic tritium charge exchange neutral bombardment is a potentially serious problem area for advanced D-T reactors operating at elevated temperatures. High concentrations of tritium in the near surface region can be reached by implantation of the charge neutral flux combined with a relatively slow recombination of these atoms into molecules at the plasma/ first wall interface. A concentration gradient is established, causing tritium to diffuse into the bulk and essentially to the outer wall surface where it can enter the first wall coolant. Since tritium separation from cooling water is very costly, release of even a small fraction of tritium to the environment could pose undesirable safety problems. Therefore, it is necessary to reduce the tritium permeation. An analysis of the way of inhibition has been made. The tritium interacts with the solid surface of the plasma facing components, resulting in trapping and material erosion, and posing problems with respect to plasma density control. The erosion of the plasma facing component materials is mainly caused by physical and chemical erosion. A detailed analysis of chemical erosion by tritium has been performed and the results are described. (author)

  10. Automation system for tritium contaminated surface monitoring

    International Nuclear Information System (INIS)

    Culcer, Mihai; Iliescu, Mariana; Curuia, Marian; Raceanu, Mircea; Enache, Adrian; Stefanescu, Ioan; Ducu, Catalin; Malinovschi, Viorel

    2005-01-01

    The low energy of betas makes tritium difficult to detect. However, there are several methods used in tritium detection, such as liquid scintillation and ionization chambers. Tritium on or near a surface can be also detected using proportional counter and, recently, solid state devices. The paper presents our results in the design and achievement of a surface tritium monitor using a PIN photodiode as a solid state charged particle detector to count betas emitted from the surface. That method allows continuous, real-time and non-destructively measuring of tritium. (authors)

  11. Tritium compatibility of alumina and Fosterite

    Energy Technology Data Exchange (ETDEWEB)

    Coffin, D.O.

    1979-09-01

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

  12. Management of tritium at nuclear facilities

    International Nuclear Information System (INIS)

    1984-01-01

    This report presents extending summaries of the works of the participants to an IAEA co-ordinated research programme, ''Handling Tritium - bearing effluents and wastes''. The subjects covered include production of tritium in nuclear power plants (mainly heavy water and light water reactors), as well as at reprocessing plants; removal and enrichment of tritium at nuclear facilities; conditioning methods and characteristics of immobilized tritium of low and high concentration; some potential methods of storage and disposal of tritium. In addition to the conclusions of this three-years work, possible activities in the field are recommended

  13. 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)

  14. Tritium control and capture in salt-cooled fission and fusion reactors: Status, challenges, and path forward

    International Nuclear Information System (INIS)

    Forsberg, Charles W.; Lam, Stephen; Carpenter, David M.; Whyte, Dennis G.; Scarlat, Raluca

    2017-01-01

    Three advanced nuclear power systems use liquid salt coolants that generate tritium and thus face the common challenges of containing and capturing tritium to prevent its release to the environment. The Fluoride-salt-cooled High-temperature Reactor (FHR) uses clean fluoride salt coolants and the same graphite-matrix coated-particle fuel as high-temperature gas-cooled reactors. Molten salt reactors (MSRs) dissolve the fuel in a fluoride or chloride salt with release of fission product tritium into the salt. In most FHR and MSR systems, the base-line salts contain lithium where isotopically separated "7Li is proposed to minimize tritium production from neutron interactions with the salt. The Chinese Academy of Science plans to start operation of a 2-MWt molten salt test reactor by 2020. For high-magnetic-field fusion machines, the use of lithium enriched in "6Li is proposed to maximize tritium generation the fuel for a fusion machine. Advances in superconductors that enable higher power densities may require the use of molten lithium salts for fusion blankets and as coolants. Recent technical advances in these three reactor classes have resulted in increased government and private interest and the beginning of a coordinated effort to address the tritium control challenges in 700 °C liquid salt systems. We describe characteristics of salt-cooled fission and fusion machines, the basis for growing interest in these technologies, tritium generation in molten salts, the environment for tritium capture, models for high-temperature tritium transport in salt systems, alternative strategies for tritium control, and ongoing experimental work. Several methods to control tritium appear viable. Finally, limited experimental data is the primary constraint for designing efficient cost-effective methods of tritium control.

  15. 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

  16. Investigation into chromatographic decomposition of tritium labelled aminoacid racemates

    International Nuclear Information System (INIS)

    Myasoedov, N.F.; Zolotarev, Yu.A.; Penkina, V.I.; Petrenik, O.V.

    1983-01-01

    Results of investigations of ligand-exchange chromatography of amino acids racemates on asymmetric sorbent containing L-oxy-proline groups in polystyrene carcass, and filled with copper ions, are described. Conditions are chosen for ligand-exchange chromatography of amino acids with high specific radioactivity labelled with tritium providing quantitative decomposition of racemates for several hours. Sorbent on polyacryl amide carcass is synthesized, the possibility of its application for the separation of amino acid racemates is studied

  17. Seasonal variations of bomb tritium in rain

    Energy Technology Data Exchange (ETDEWEB)

    Israel, G.; Roether, W.; Schumann, G.

    1962-08-15

    The tritium activity of precipitation at Sindorf, near Cologne, Germany, has been monitored since 1960. Experimental results are presented and discussed briefly with the aid of a comparison to Sr/sup 90/ as another artificial nuclide characterized by similar tropospheric behavior. (auth) A series of analytical schemes for the measurement of Ba/sup 140/, Sr/sup 89/, Sr/sup 90/, Cs/sup 137/, I/sup 131/, and Pu/sup 238/ in various environmental materials is described. These procedures are based on radiochemical methods in use at Chalk River and have been thoroughly tested in practice. The manual is divided into distinct sections in the belief that such an arrangement will be a convenience where sample preparation, gamma -spectrometry, radiochemistry, and counting are performed by different people working in separate areas of a laboratory. (auth)

  18. Weapons engineering tritium facility overview

    Energy Technology Data Exchange (ETDEWEB)

    Najera, Larry [Los Alamos National Laboratory

    2011-01-20

    Materials provide an overview of the Weapons Engineering Tritium Facility (WETF) as introductory material for January 2011 visit to SRS. Purpose of the visit is to discuss Safety Basis, Conduct of Engineering, and Conduct of Operations. WETF general description and general GTS program capabilities are presented in an unclassified format.

  19. Tritium-labelled abscisic acid

    International Nuclear Information System (INIS)

    Pluciennik, H.; Michalski, L.

    1991-01-01

    A simple method for the preparation of biologically active abscisic acid (growth inhibiting plant hormone) labelled with tritium is described. The product obtained has a specific radioactivity of 1.12 GBq mmol -1 : the yield is about 60% as compared to the initial amount of the substance used. (author) 7 refs.; 2 figs

  20. Tritium Level in Romanian Precipitation

    Energy Technology Data Exchange (ETDEWEB)

    Varlam, C.; Stefanescu, I.; Faurescu, I.; Bogdan, D.; Soare, A. [Institute for Cryogenic and Isotope Technologies, Rm. Valcea (Romania); Duliu, O. G. [Faculty of Physics, University of Bucharest, Magurele (Romania)

    2013-07-15

    Romania is one of the countries that has no station included in GNIP (Global Network of Isotopes in Precipitation) on its territory. This paper presents results regarding the tritium concentration in precipitation for the period 1999-2009. The precipitation fell at the Institute for cryogenic and Isotope technologies (geographical coordinates: altitude 237 m, latitude 45{sup o}02'07' N, longitude 24{sup o}17'03' E) an was collected both individually and as a composite average of each month. It was individually measured and the average was calculated and compared with the tritium concentration measured in the composite sample. tritium concentration levels ranged from 9.9 {+-} 2.1 TU for 2004 and 13.7 {+-} 2.2 TU for 2009. Comparing the arithmetic mean values with the weighted mean for the period of observation, it was noticed that the higher absolute values of the weighted means were constant. It was found that for the calculated monthly average for the period of observation (1999-2009), the months with the maximum tritium concentration are the same as the months with the maximum amount of precipitation. This behaviour is typical for the monitored location. (author)

  1. Tritium transport analysis for CFETR WCSB blanket

    Energy Technology Data Exchange (ETDEWEB)

    Zhao, Pinghui, E-mail: phzhao@mail.ustc.edu.cn; Yang, Wanli; Li, Yuanjie; Ge, Zhihao; Nie, Xingchen; Gao, Zhongping

    2017-01-15

    Highlights: • A simplified tritium transport model for CFETR WCSB blanket was developed. • Tritium transport process in CFETR WCSB blanket was analyzed. • Sensitivity analyses of tritium transport parameters were carried out. - Abstract: Water Cooled Solid Breeder (WCSB) blanket was put forward as one of the breeding blanket candidate schemes for Chinese Fusion Engineering Test Reactor (CFETR). In this study, a simplified tritium transport model was developed. Based on the conceptual engineering design, neutronics and thermal-hydraulic analyses of CFETR WCSB blanket, tritium transport process was analyzed. The results show that high tritium concentration and inventory exist in primary water loop and total tritium losses exceed CFETR limits under current conditions. Conducted were sensitivity analyses of influential parameters, including tritium source, temperature, flow-rate capacity and surface condition. Tritium performance of WCSB blanket can be significantly improved under a smaller tritium impinging rate, a larger flow-rate capacity or a better surface condition. This work provides valuable reference for the enhancement of tritium transport behavior in CFETR WCSB blanket.

  2. Tritium behavior intentionally released in the room

    International Nuclear Information System (INIS)

    Kobayashi, K.; Hayashi, T.; Iwai, Y.; Yamanishi, T.; Willms, R. S.; Carlson, R. V.

    2008-01-01

    To construct a fusion reactor with high safety and acceptability, it is necessary to establish and to ensure tritium safe handling technology. Tritium should be well-controlled not to be released to the environment excessively and to prevent workers from excess exposure. It is especially important to grasp tritium behavior in the final confinement area, such as the room and/or building. In order to obtain data for actual tritium behavior in a room and/or building, a series of intentional Tritium Release Experiments (TREs) were planned and carried out within a radiologically controlled area (main cell) at Tritium System Test Assembly (TSTA) in Los Alamos National Laboratory (LANL) under US-JAPAN collaboration program. These experiments were carried out three times. In these experiments, influence of a difference in the tritium release point and the amount of hydrogen isotope for the initial tritium behavior in the room were suggested. Tritium was released into the main cell at TSTA/LANL. The released tritium reached a uniform concentration about 30 - 40 minutes in all the experiments. The influence of the release point and the amount of hydrogen isotope were not found to be important in these experiments. The experimental results for the initial tritium behavior in the room were also simulated well by the modified three-dimensional eddy flow analysis code FLOW-3D. (authors)

  3. Tritium migration in nuclear desalination plants

    International Nuclear Information System (INIS)

    Muralev, E.D.

    2003-01-01

    Tritium transport, as one of important items of radiation safety assessment, should be taken into consideration before construction of a Nuclear Desalination Plant (NDP). The influence of tritium internal exposition to the human body is very dangerous because of 3 H associations with water molecules. The problem of tritium in nuclear engineering is connected to its high penetration ability (through fuel element cans and other construction materials of a reactor), with the difficulty of extracting tritium from process liquids and gases. Sources of tritium generation in NDP are: nuclear fuel, boron in control rods, and deuterium in heat carrier. Tritium passes easily through the walls of a reactor vessel, intermediate heat exchangers, steam generators and other technological equipment, through the walls of heat carrier pipelines. The release of tritium and its transport could be assessed, using mathematical models, based on the assumption that steady state equilibrium has been attained between the sources of tritium, produced water and release to the environment. Analysis of the model shows the tritium concentration dependence in potable water on design features of NDP. The calculations obtained and analysis results for NDP with BN-350 reactor give good convergence. According to the available data, tritium concentration in potable water is less than the statutory maximum concentration limit. The design of a NDP requires elaboration of technical solutions, capable of minimising the release of tritium to potable water produced. (author)

  4. A compact, low cost, tritium removal plant for CANDU-6 reactors

    International Nuclear Information System (INIS)

    Sood, S.K.; Fong, C.; Kalyanam; Woodall, K.B.

    1997-01-01

    Tritium concentrations in CANDU-6 reactors are currently around 40 Ci/kg in moderator systems and around 1.5 Ci/kg in primary heat transport (PHT) systems. It is expected that tritium concentrations in moderator systems will continue to rise and will reach about 80 Ci/kg at maturity. A more detailed description of the increase in tritium concentrations in the moderator and PHT systems of CANDU-6 reactors is given in the next section of this paper. While moderator systems currently contribute more than 50% to tritium emissions, the impact of acute releases of moderator water is more severe at higher tritium concentrations. This impact can be substantially reduced by the addition of an isotope separation system for lowering the tritium level in the moderator system. In addition, lower tritium levels in CANDU systems will inevitably result in reduced occupational exposures, or will provide economic benefits due to ease of maintenance because less protective measures are required and maintenance activities can be more efficient

  5. Storage and Assay of Tritium in STAR

    International Nuclear Information System (INIS)

    Longhurst, Glen R.; Anderl, Robert A.; Pawelko, Robert J.; Stoots, Carl J.

    2005-01-01

    The Safety and Tritium Applied Research (STAR) facility at the Idaho National Engineering and Environmental Laboratory (INEEL) is currently being commissioned to investigate tritium-related safety questions for fusion and other technologies. The tritium inventory for the STAR facility will be maintained below 1.5 g to avoid the need for STAR to be classified as a Category 3 nuclear facility. A key capability in successful operation of the STAR facility is the ability to receive, inventory, and dispense tritium to the various experiments underway there. The system central to that function is the Tritium Storage and Assay System (SAS).The SAS has four major functions: (1) receiving and holding tritium, (2) assaying, (3) dispensing, and (4) purifying hydrogen isotopes from non-hydrogen species.This paper describes the design and operation of the STAR SAS and the procedures used for tritium accountancy in the STAR facility

  6. Tritium pellet injection sequences for TFTR

    International Nuclear Information System (INIS)

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

    1983-01-01

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

  7. Imaging of tritium implanted into graphite

    International Nuclear Information System (INIS)

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

    1988-01-01

    The extensive use of graphite in plasma-facing surfaces of tokamaks such as the Tokamak Fusion Test Reactor, which has planned tritium discharges, makes two-dimensional tritium detection techniques important in helping to determine torus tritium inventories. We have performed experiments in which highly oriented pyrolytic graphite (HOPG) samples were first tritium implanted with fluences of ∼10 16 T/cm 2 at energies approx. 0 C resulted in no discernible motion of tritium along the basal plane, but did show that significant desorption of the implanted tritium occurred. The current results indicate that tritium in quantities of 10 12 T/cm 2 in tritiated components could be readily detected by imaging at lower magnifications

  8. Calculation of tritium release from reactor's stack

    International Nuclear Information System (INIS)

    Akhadi, M.

    1996-01-01

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

  9. Tritium systems test assembly stabilization

    International Nuclear Information System (INIS)

    Jasen, William G.; Michelotti, Roy A.; Anast, Kurt R.; Tesch, Charles

    2004-01-01

    The Tritium Systems Test Assembly (TSTA) was a facility dedicated to tritium technology Research and Development (R and D) primarily for future fusion power reactors. The facility was conceived in mid 1970's, operations commenced in early 1980's, stabilization and deactivation began in 2000 and were completed in 2003. The facility will remain in a Surveillance and Maintenance (S and M) mode until the Department of Energy (DOE) funds demolition of the facility, tentatively in 2009. A safe and stable end state was achieved by the TSTA Facility Stabilization Project (TFSP) in anticipation of long term S and M. At the start of the stabilization project, with an inventory of approximately 140 grams of tritium, the facility was designated a Hazard Category (HC) 2 Non-Reactor Nuclear facility as defined by US Department of Energy standard DOE-STD-1027-92 (1997). The TSTA facility comprises a laboratory area, supporting rooms, offices and associated laboratory space that included more than 20 major tritium handling systems. The project's focus was to reduce the tritium inventory by removing bulk tritium, tritiated water wastes, and tritium-contaminated high-inventory components. Any equipment that remained in the facility was stabilized in place. All of the gloveboxes and piping were rendered inoperative and vented to atmosphere. All equipment, and inventoried tritium contamination, remaining in the facility was left in a safe-and-stable state. The project used the End Points process as defined by the DOE Office of Environmental Management (web page http://www.em.doe.- gov/deact/epman.htmtlo) document and define the end state required for the stabilization of TSTA Facility. The End Points process added structure that was beneficial through virtually all phases of the project. At completion of the facility stabilization project the residual tritium inventory was approximately 3,000 curies, considerably less than the 1.6-gram threshold for a HC 3 facility. TSTA is now

  10. Tritium issues in plasma wall interactions

    International Nuclear Information System (INIS)

    Tanabe, T.

    2009-01-01

    In order to establish a D-T fusion reactor as an energy source, it is not enough to have a DT burning plasma, and economical conversion of fusion energy to electricity and/or heat, a large enough margin of tritium breeding and tritium safety must be simultaneously achieved. In particular, handling of huge amount of tritium needs a significant effort to ensure that the radiation dose of radiological workers and of the public is below the limits specified by the International Commission on Radiological Protection. For the safety reasons, tritium in a reactor will be limited to only a few kg orders in weight, with radioactivity up to 10 17 Bq. Since public exposure to tritium is regulated at a level as tiny as a few Bq/cm 2 , tritium must be strictly confined in a reactor system with accountancy of an order of pg (pico-gram). Generally qualitative analysis with the accuracy of more than 3 orders of magnitude is hardly possible. We are facing to lots of safety concerns in the handling of huge amounts of radioactive tritium as a fuel and to be bred in a blanket. In addition, tritium resources are very limited. Not only for the safety reason but also for the saving of tritium resources, tritium retention in a reactor must be kept as small as possible. In the present tokamaks, however, hydrogen retention is significantly large, i.e. more than 20% of fueled hydrogen is continuously piled up in the vacuum vessel, which must not be allowed in a reactor. After the introduction of tritium as a hydrogen radioisotope, this lecture will present tritium issues in plasma wall interactions, in particular, fueling, retention and recovering, considering the handling of large amounts of tritium, i.e. confinement, leakage, contamination, permeation, regulations and tritium accountancy. Progress in overcoming such problems will be also presented. This document is made of the slides of the presentation. (author)

  11. 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)

  12. Isotope separations using chromatographic methods

    International Nuclear Information System (INIS)

    Leseticky, L.

    1985-01-01

    A survey is given of chromatographic separations of compounds only differing in isotope composition. Isotope effects on physical properties which allow chromatographic separation (vapour tension, adsorption heat, partition coefficient) are very small, with the exception of the simplest molecules. Therefore, separation factors only assume the value of several per cent. From this ensues the necessity of using columns which are specially and very carefully prepared and have a separation efficiency of the order of 10 4 theoretical plates. Briefly discussed is liquid chromatography on ion exchangers which with a varied degree of success was used for separating simple inorganic compounds or ions. Ion exchange chromatography of amino acids labelled with tritium, and chromatography of tritium labelled steroids also provided only a certain degree of separation. A detailed analysis is presented of gas chromatography separation of various deuterium and tritium labelled low-molecular compounds, to which a number of studies has been devoted in the literature. Very promising is the method of complexation gas chromatography based on the reversible formation of a complex of the ligand (the compound being separated) and the compound of the (transition) metal as the steady-state phase. (author)

  13. Hydrogen isotope separation experience at the Savannah River Site

    International Nuclear Information System (INIS)

    Lee, M.W.

    1993-01-01

    Savannah River Site (SRS) is a sole producer of tritium for US Weapons Program. SRS has built Facilities, developed the tritium handling processes, and operated safely for the last forty years. Tritium is extracted from the irradiated reactor target, purified, mixed with deuterium, and loaded to the booster gas bottle in the weapon system for limited lifetime. Tritium is recovered from the retired bottle and recycled. Newly produced tritium is branded into the recycled tritium. One of the key process is the hydrogen isotope separation that tritium is separated from deuterium and protium. Several processes have been used for the hydrogen isotope separation at SRS: Thermal Diffusion Column (TD), Batch Cryogenic Still (CS), and Batch Chromatography called Fractional Sorption (FS). TD and CS requires straight vertical columns. The overall system separation factor depends on the length of the column. These are three story building high and difficult to put in glove box. FS is a batch process and slow operation. An improved continuous chromatographic process called Thermal Cycling Absorption Process (TCAP) has been developed. It is small enough to be about to put in a glove box yet high capacity comparable to CS. The SRS tritium purification processes can be directly applicable to the Fusion Fuel Cycle System of the fusion reactor

  14. TRITIUM IN URINE OF PEOPLE LIVING IN THE AREA OF INFLUENCE OF THE BELOYARSKAYA NPP

    Directory of Open Access Journals (Sweden)

    M. Ya. Chebotina

    2016-01-01

    Full Text Available The goal of the research is to determine relationship between tritium concentration in the body fluid (urine of people living in the area of influence of the Beloyarskaya NPP and tritium concentration in drinking water.Materials and methods. Studed population (men and women. Urine samples were collected in the clinical laboratory of a medical unit in Zarechny town. There were 50 individuals in the studied group. Patients were different on age and weight. Water samples were collected in an arbitrary way, through the all study period, from October to November in 2015 year. Tritium concentrations were determined with the ultra-low level liquid scintillation spectrometer Quantulus-1220 (USA. The facility developed by L.G. Bondareva was used for tritium extraction. The method allowes to separate the template, which significantly effects determination of tritium.Results. The urine samples from people living in the area of influence of the Beloyarskaya NPP in Zarechny town were analyzed in the study. There was positive relationship between tritium concentration in drinking water and tritium concentration in urine. Statistically significant correlation between analyzed parameters was found (correlation coefficient 0.98; significance level 0,007. Individual doses were estimated according to Harrison, Khursheed, Lambert. The Doses vary from 0,32 to 1,12 with an allowance for consumption of drinking water 100 l y–1 (according to the consumption standard for the analyzed region, which amounts 0,032–0,12 % from dose limit for population (1 mSv y–1. It was determined what drinking water is the main source of the radionuclide in human body in this region. The determined values of tritium concentration in drinking water are significantly lower than the intervention level for tritium of 7600 Bq l–1 ( Radiation Safety Standards-99/2009, Appendix 2a.

  15. A phantom for assessing the personal dose equivalent, H{sub P}(10); Um fantoma para a avaliacao do equivalente de dose pessoal, H{sub P}(10).

    Energy Technology Data Exchange (ETDEWEB)

    Santoro, C.; Filho, J.A [Universidade Federal de Pernambuco (UFPE), Recife, PE (Brazil). Departamento de Energia Nuclear; Santos, M.A.P.; Filho, L.C.G., E-mail: chsantoro@gmail.com, E-mail: masantos@cnen.gov.br, E-mail: l.filho@cnen.gov.br, E-mail: jaf@ufpe.br [Centro Regional de Ciencias Nucleares do Nordeste (CRCN-NE/CNEN-PE), Recife, PE (Brazil)

    2013-10-15

    Characteristics of a phantom designed to evaluate the personal dose equivalent, H{sub P}(10), and appropriate for photographic dosimetry are presented. It is called HP(10) phantom due to cavities constructed to insert dosimetric films at a depth of 10 mm. The H{sub P}(10) phantom is irradiated with ionizing radiation energy, E, from 45 to 1250 keV, with doses ranging from 0.2 to 50 mSv. It is positioned in the direction α = 0 °, and the radiation field focusing perpendicular to its front surface. So, are established calibration curves of dosimeters in the position conventionally true and quantities H{sub P}(10). It made a comparison between the responses obtained with the H{sub P}(10) phantom and responses obtained when using the calibration procedure recommended by ISO dosimeters. The ISO recommends getting the air kerma, Ka, for photons at test point of the radiation field by an ionization chamber. And through conversion coefficients, h{sub pK} (10; E, α), becomes the air kerma for H{sub P}(10). The ISO 4037-3 recommendation has been studied by researchers to ensure that the low energy spectral differences occur in radiation fields which are generated by various X-ray equipment, and induce changes in the percentages of conversion coefficients on the order of 10% to 90% . On the basis of the recommendations ISO, this article develops phantom able to assess the dose to the influence of scattering and absorption of radiation, its implications with respect to dosimetry, providing improvement in the assessment of doses. (author)

  16. ITER safety task NID-5a: ITER tritium environmental source terms - safety analysis basis

    International Nuclear Information System (INIS)

    Natalizio, A.; Kalyanam, K.M.

    1994-09-01

    The Canadian Fusion Fuels Technology Project's (CFFTP) is part of the contribution to ITER task NID-5a, Initial Tritium Source Term. This safety analysis basis constitutes the first part of the work for establishing tritium source terms and is intended to solicit comments and obtain agreement. The analysis objective is to provide an early estimate of tritium environmental source terms for the events to be analyzed. Events that would result in the loss of tritium are: a Loss of Coolant Accident (LOCA), a vacuum vessel boundary breach. a torus exhaust line failure, a fuelling machine process boundary failure, a fuel processing system process boundary failure, a water detritiation system process boundary failure and an isotope separation system process boundary failure. 9 figs

  17. R and D of tritium technology as SHI (Sumitomo Heavy Industries)

    International Nuclear Information System (INIS)

    Yokogawa, N.

    1997-01-01

    Sumitomo Heavy Industries (SHI) participated in an R and D programme on tritium processing for the first time in 1967 by joining the advanced thermal reactor project. (The thermal reactor is cooled by light water and moderated by heavy water.) From that time SHI has developed various kind of tritium handling technologies. On the basis of cooperation with Sulzer (Sulzer Chemtech Ltd. Switzerland), SHI developed a system for removing waste water for fuel reprocessing plants by water distillation technology. In the field of fusion technology, SHI has developed a hydrogen isotope separation system by cryogenic distillation and thermal diffusion methods, and a tritium storage bed. Fundamental data required for the system design were obtained through the production and operation of the above prototype systems. Recently, SHI has also been taking part in the design and planning of ITER. In the future, along with ITER design, SHI will aim at developing tritium measuring technology. (author)

  18. Status and practicality of detritiation and tritium production strategies for environmental remediation

    Energy Technology Data Exchange (ETDEWEB)

    Fulbright, H.H.; Schwirian-Spann, A.L.; Brunt, V. van [Univ. of South Carolina, Columbia, SC (US); Jerome, K.M.; Looney, B.B. [Westinghouse Savannah River Co., Aiken, SC (US)

    1996-02-26

    Operation of nuclear facilities throughout the world generates wastewater, groundwater and surface water contaminated with tritium. Because of a commitment to minimize radiation exposures to ''levels as low as reasonably achievable'', the US Department of Energy supports development of tritium isotope separation technologies. Also, DOE periodically documents the status and potential viability of alternative tritium treatment technologies and management strategies. The specific objectives of the current effort are to evaluate practical engineering issues, technology acceptability issues, and costs for realistic tritium treatment scenarios. A unique feature of the assessment is that the portfolio of options was expanded to include various management strategies rather than only evaluating detritiation technologies. The ultimate purpose of this effort is to assist Environmental Restoration and its support organizations in allocating future investments.

  19. Monitoring tritium in air containing other beta-emitters using ion chambers

    International Nuclear Information System (INIS)

    Jalbert, R.A.

    1975-01-01

    A flow-through ionization chamber instrument is described which is capable of measuring tritium in air containing high concentrations of other beta emitters. The instrument employs a separate concentric chamber with a thin common wall opaque only to tritium betas. Currents produced in the two chambers are subtracted leaving only the current due to tritium. With a 1.6-l sampling chamber and an 18-s time constant, tritium concentrations of 10 -6 μCi/ml to 10 -4 μCi/ml are measured with 2 sigma confidence in background beta concentrations of 4 x 10 -5 μCi/ml to 0.4 muCi/ml, respectively. (auth)

  20. Status and practicality of detritiation and tritium production strategies for environmental remediation

    International Nuclear Information System (INIS)

    Fulbright, H.H.; Schwirian-Spann, A.L.; Brunt, V. van; Jerome, K.M.; Looney, B.B.

    1996-01-01

    Operation of nuclear facilities throughout the world generates wastewater, groundwater and surface water contaminated with tritium. Because of a commitment to minimize radiation exposures to ''levels as low as reasonably achievable'', the US Department of Energy supports development of tritium isotope separation technologies. Also, DOE periodically documents the status and potential viability of alternative tritium treatment technologies and management strategies. The specific objectives of the current effort are to evaluate practical engineering issues, technology acceptability issues, and costs for realistic tritium treatment scenarios. A unique feature of the assessment is that the portfolio of options was expanded to include various management strategies rather than only evaluating detritiation technologies. The ultimate purpose of this effort is to assist Environmental Restoration and its support organizations in allocating future investments

  1. Tritium sorption by cement and subsequent release

    International Nuclear Information System (INIS)

    Ono, F.; Yamawaki, M.

    1995-01-01

    In a fusion reactor or tritium-handling facilities, contamination of concrete by tritium and subsequent release from it to the reator or experimental room is a matter of problem for safe control of tritium and management of operational environment. In order to evaluate this tritium behavior, interaction of tritiated water with concrete or cement should be clarified. In the present study, HTO sorption and subsequent release from cement were experimentally studied.(1)Sorption experiments were conducted using columns packed with cement particles of different sizes. From the analysis of the breakthrough curve, tritium diffusivity in macropores and microparticles were evaluated.(2)From the short-term tritium release experiments, effective desorption rate constants were evaluated and the effects of temperature and moisture were studied.(3)In the long-term tritium release experiments to 6000h, the tritium release mechanism was found to be composed of three kinds of water: initially from capillary water, and in the second stage from gel water and from the water in the cement crystal.(4)Tritium release behavior by heat treatment to 800 C was studied. A high temperature above 600 C was required for the tritium trapped in the crystal water to be released. (orig.)

  2. The LLNL portable tritium processing system

    International Nuclear Information System (INIS)

    Anon.

    1995-01-01

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

  3. Estimation of Biological Effects of Tritium.

    Science.gov (United States)

    Umata, Toshiyuki

    2017-01-01

    Nuclear fusion technology is expected to create new energy in the future. However, nuclear fusion requires a large amount of tritium as a fuel, leading to concern about the exposure of radiation workers to tritium beta radiation. Furthermore, countermeasures for tritium-polluted water produced in decommissioning of the reactor at Fukushima Daiichi Nuclear Power Station may potentially cause health problems in radiation workers. Although, internal exposure to tritium at a low dose/low dose rate can be assumed, biological effect of tritium exposure is not negligible, because tritiated water (HTO) intake to the body via the mouth/inhalation/skin would lead to homogeneous distribution throughout the whole body. Furthermore, organically-bound tritium (OBT) stays in the body as parts of the molecules that comprise living organisms resulting in long-term exposure, and the chemical form of tritium should be considered. To evaluate the biological effect of tritium, the effect should be compared with that of other radiation types. Many studies have examined the relative biological effectiveness (RBE) of tritium. Hence, we report the RBE, which was obtained with radiation carcinogenesis classified as a stochastic effect, and serves as a reference for cancer risk. We also introduce the outline of the tritium experiment and the principle of a recently developed animal experimental system using transgenic mouse to detect the biological influence of radiation exposure at a low dose/low dose rate.

  4. 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

  5. The tritium content of precipitation and groundwater at Yola, Nigeria ...

    African Journals Online (AJOL)

    Tritium is a radioactive isotope of hydrogen which occurs in precipitation. In groundwater studies tritium measurements give information on the time of recharge to the system; the tritium content of precipitation being used to estimate the input of tritium to the groundwater system. At Yola, the tritium ontents in precipitation and ...

  6. Tritium in Exit Signs | RadTown USA | US EPA

    Science.gov (United States)

    2017-08-07

    Many exit signs contain tritium to light the sign without batteries or electricity. Using tritium in exit signs allows the sign to remain lit if the power goes out. Tritium is most dangerous when it is inhaled or swallowed. Never tamper with a tritium exit sign. If a tritium exit sign is broken, leave the area immediately and notify the building maintenance staff.

  7. 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)

  8. From whales to tritium

    International Nuclear Information System (INIS)

    Bonnemains, J.

    2007-01-01

    Only 150 years of human actions and innovations separate whale-oil lamps from atomic fission and fusion. During this period, the human quest for lighting, heating and transportation has drained the stock of fuels, ranging from peat and wood to coal and petroleum. The energy necessary for protecting us from the cold and heat, for transportation, lighting and other comforts is a persistent problem. Since the start of the industrial era and the consumer age, the solutions adopted have jeopardized the oceans, atmosphere and earth. (author)

  9. 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

  10. Radiological safety system based on real-time tritium-in-air monitoring indoors and in effluents

    International Nuclear Information System (INIS)

    Bidica, N.; Sofalca, N; Balteanu, O.; Srefan, I.

    2006-01-01

    Exposure to tritium is an important health hazard in any tritium processing facility so that implementing a real-time tritium monitoring system is necessary for its operation in safety conditions. The tritium processing facility operators need to be informed at any time about the in-air tritium concentration indoors or in the stack effluents, in order to detect immediately any leaks in tritium containments, or any releases inside the buildings or to the environment. This information is very important for adopting if necessary protection measures and correcting actions as quickly as possible. In this paper we describe an improved real-time tritium monitoring system designed for the Heavy Water Detritiation Pilot Plant of National Institute for Cryogenics and Isotopes Separation, Rm. Valcea, Romania. The design of the Radiological Safety System implemented for the ICIT Water Detritiation Pilot Plant is intended to provide the maximum safety level based on the ALARA concept. The main functions of tritium monitoring system are: - monitoring the working areas and gaseous effluents by determination of the tritium-in-air activity concentration; - local and remote data display; - assessing of environment dose equivalent rates and dose equivalents in the working environment (for personnel exposure control and work planning); - assessing the total tritium activity released to the environment through ventilation exhaust stack; - safety functions, i.e., local and remote, locking/unlocking personnel access, process shut-down in emergency conditions and start of the air cleaning systems. With all these features our tritium monitoring system is really a safety system adequate for personnel and environmental protection. (authors)

  11. 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.

  12. 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)

  13. Tritium labelled steroids, preparation process and application to synthesis of tritium labelled estrane derivatives

    International Nuclear Information System (INIS)

    1978-01-01

    Process for preparing new steroids labelled with tritium in 6.7 and comprising in 3 a blocked ketonic group as ketal, thioketal or derivatives. Application of these products to the synthesis of tritium labelled estrane derivatives [fr

  14. Radiological training for tritium facilities

    International Nuclear Information System (INIS)

    1996-12-01

    This program management guide describes a recommended implementation standard for core training as outlined in the DOE Radiological Control Manual (RCM). The standard is to assist those individuals, both within DOE and Managing and Operating contractors, identified as having responsibility for implementing the core training recommended by the RCM. This training may also be given to radiological workers using tritium to assist in meeting their job specific training requirements of 10 CFR 835

  15. Radiological training for tritium facilities

    Energy Technology Data Exchange (ETDEWEB)

    NONE

    1996-12-01

    This program management guide describes a recommended implementation standard for core training as outlined in the DOE Radiological Control Manual (RCM). The standard is to assist those individuals, both within DOE and Managing and Operating contractors, identified as having responsibility for implementing the core training recommended by the RCM. This training may also be given to radiological workers using tritium to assist in meeting their job specific training requirements of 10 CFR 835.

  16. Analytical similarity assessment of rituximab biosimilar CT-P10 to reference medicinal product.

    Science.gov (United States)

    Lee, Kyoung Hoon; Lee, Jihun; Bae, Jin Soo; Kim, Yeon Jung; Kang, Hyun Ah; Kim, Sung Hwan; Lee, So Jung; Lim, Ki Jung; Lee, Jung Woo; Jung, Soon Kwan; Chang, Shin Jae

    2018-04-01

    CT-P10 (Truxima™) was recently approved as the world's first rituximab biosimilar product in the European Union (EU) and South Korea. To demonstrate biosimilarity of CT-P10 with the reference medicinal product (RMP), extensive 3-way similarity assessment has been conducted between CT-P10, EU-Rituximab and US-Rituximab, focusing on the physicochemical and biological quality attributes. A multitude of state-of-the-art analyses revealed that CT-P10 has identical primary and higher order structures compared to the original product. Purity/impurity profiles of CT-P10 measured by the levels of aggregates, fragments, non-glycosylated form and process-related impurities were also found to be comparable with those of RMPs. In terms of the post-translational modification, CT-P10 contains slightly less N-terminal pyro-glutamate variant, which has been known not to affect product efficacy or safety. Oligosaccharide profiling has revealed that, although CT-P10 contains the same conserved glycan species and relative proportion with the RMPs, the content of total afucosylated glycan in CT-P10 was slightly higher than in EU- or US-Rituximab. Nevertheless, the effect of the observed level of afucosylation in CT-P10 drug product on Fc receptor binding affinity or antibody-dependent cell-mediated cytotoxicity was found to be negligible based on the spiking study with highly afucosylated sample. Arrays of biological assays representative of known and putative mechanisms of action for rituximab have shown that biological activities of CT-P10 are within the quality range of RMPs. Recent results of clinical studies have further confirmed that the CT-P10 exhibits equivalent clinical efficacy and safety profiles compared to EU- and US-Rituximab. The current 3-way similarity assessment together with clinical study results confidently demonstrate that CT-P10 is highly similar with EU- and US-Rituximab in terms of physicochemical properties, biological activities, efficacy, and safety for

  17. Tritium environmental transport studies at TFTR

    International Nuclear Information System (INIS)

    Ritter, P.D.; Dolan, T.J.; Longhurst, G.R.

    1993-01-01

    Environmental tritium concentrations will be measured near the Tokamak Fusion Test Reactor (TFTR) to help validate dynamic models of tritium transport in the environment. For model validation the database must contain sequential measurements of tritium concentrations in key environmental compartments. Since complete containment of tritium is an operational goal, the supplementary monitoring program should be able to glean useful data from an unscheduled acute release. Portable air samplers will be used to take samples automatically every 4 hours for a weak after an acute release, thus obtaining the time resolution needed for code validation. Samples of soil, vegetation, and foodstuffs will be gathered daily at the same locations as the active air monitors. The database may help validate the plant/soil/air part of tritium transport models and enhance environmental tritium transport understanding for the International Thermonuclear Experimental Reactor (ITER)

  18. Tritium environmental transport studies at TFTR

    Science.gov (United States)

    Ritter, P. D.; Dolan, T. J.; Longhurst, G. R.

    1993-06-01

    Environmental tritium concentrations will be measured near the Tokamak Fusion Test Reactor (TFTR) to help validate dynamic models of tritium transport in the environment. For model validation the database must contain sequential measurements of tritium concentrations in key environmental compartments. Since complete containment of tritium is an operational goal, the supplementary monitoring program should be able to glean useful data from an unscheduled acute release. Portable air samplers will be used to take samples automatically every 4 hours for a week after an acute release, thus obtaining the time resolution needed for code validation. Samples of soil, vegetation, and foodstuffs will be gathered daily at the same locations as the active air monitors. The database may help validate the plant/soil/air part of tritium transport models and enhance environmental tritium transport understanding for the International Thermonuclear Experimental Reactor (ITER).

  19. 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)

  20. Modeling tritium transport in the environment

    International Nuclear Information System (INIS)

    Murphy, C.E. Jr.

    1986-01-01

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

  1. Tritium Removal from Carbon Plasma Facing Components

    International Nuclear Information System (INIS)

    Skinner, C.H.; Coad, J.P.; Federici, G.

    2003-01-01

    Tritium removal is a major unsolved development task for next-step devices with carbon plasma-facing components. The 2-3 order of magnitude increase in duty cycle and associated tritium accumulation rate in a next-step tokamak will place unprecedented demands on tritium removal technology. The associated technical risk can be mitigated only if suitable removal techniques are demonstrated on tokamaks before the construction of a next-step device. This article reviews the history of codeposition, the tritium experience of TFTR (Tokamak Fusion Test Reactor) and JET (Joint European Torus) and the tritium removal rate required to support ITER's planned operational schedule. The merits and shortcomings of various tritium removal techniques are discussed with particular emphasis on oxidation and laser surface heating

  2. Comparison of Tritium Component Failure Rate Data

    International Nuclear Information System (INIS)

    Lee C. Cadwallader

    2004-01-01

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

  3. Effects of interfering constituents on tritium smears

    International Nuclear Information System (INIS)

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

    1993-01-01

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

  4. 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)

  5. Behaviour of tritium in the plant domain

    International Nuclear Information System (INIS)

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

    1979-01-01

    An attempt is made to review in three different ways the present status regarding the uptake, retention and release patterns of plants of different trophic levels exposed to a tritiated atmosphere. The mean residence time for the first major component is found to be within 1-12 days for all the terrestrial vegetations. The second and the third components form only a small fraction of the total tritium uptake and show significantly different mean residence times. The aquatic plant, Hydrilla verticellata, also shows very small residence time for the first component (0.4 h). An isotopic discrimination of about 30-40% against the incorporation of tissue-bound tritium (TBT) is found in some algal and aquatic species, and this is enhanced to as high as 90-99% for the terrestrial vegetations. When conditions of constant specific activity are maintained, even for the terrestrial vegetations high specific activity ratios are obtained in the few cases cited. The nucleic acid fraction has shown relative specific activity ratios of 0.37 and 1.0 for pea seedlings and algae respectively. In maize, though carbohydrate is a major fraction fat has shown maximum fixation of TBT. Mathematical resolution procedures to determine the mean residence times for TFWT/TBT fractions either from separated or composite sample fractions have been reviewed. TFWT time-activity profiles are built up for succulent plants from diffusion, xylem flow and the utilization of TFWT in the synthesis of TBT. A good agreement between the calculated and experimental values is obtained using molecular diffusion coefficients for succulent plants. The applicability of this concept for larger trees is discussed

  6. Regulating tritium in drinking water

    International Nuclear Information System (INIS)

    Fluke, R.

    1994-01-01

    This article incorporates an article by E. Koehl from an internal Ontario Hydro publication, and a letter from the Joint Committee of Health and Safety of the Royal Society of Canada and the Canadian Academy of Engineering, submitted to the Ontario Minister of the Environment and Energy. The Advisory Committee on Environmental Standards had recommended that the limit for tritium in Ontario drinking water be reduced from 40,000 to 100 Bq/L, with a further reduction to 20 in five years. Some facts and figures are adduced to show that the effect of tritium in drinking water in Ontario is negligible compared to the effect of background radiation. The risk from tritium to the people of Ontario is undetectably small, and the attempt to estimate this risk by linear extrapolation is extremely dubious. Regulation entails social and economic costs, and the government ought to ensure that the benefits exceed the costs. The costs translate into nothing less than wasted opportunity to save lives in other ways. 3 refs

  7. Tritium management in fusion reactors

    International Nuclear Information System (INIS)

    Galloway, T.R.

    1978-05-01

    This is a review paper covering the key environmental and safety issues and how they have been handled in the various magnetic and inertial confinement concepts and reference designs. The issues treated include: tritium accident analyses, tritium process control, occupational safety, HTO formation rate from the gas-phase, disposal of tritium contaminated wastes, and environmental impact--each covering the Joint European Tokamak (J.E.T. experiment), Tokamak Fusion Test Reactor (TFTR), Russian T-20, The Next Step (TNS) designs by Westinghouse/ORNL and General Atomic/ANL, the ANL and ORNL EPR's, the G.A. Doublet Demonstration Reactor, the Italian Fintor-D and the ORNL Demo Studies. There are also the following full scale plant reference designs: UWMAK-III, LASL's Theta Pinch Reactor Design (RTPR), Mirror Fusion Reactor (MFR), Tandem Mirror Reactor (TMR), and the Mirror Hybrid Reactor (MHR). There are four laser device breakeven experiments, SHIVA-NOVA, LLL reference designs, ORNL Laser Fusion power plant, the German ''Saturn,'' and LLL's Laser Fusion EPR I and II

  8. Refurbishing tritium contaminated ion sources

    International Nuclear Information System (INIS)

    Wright, K.E.; Carnevale, R.H.; McCormack, B.E.; Stevenson, T.; Halle, A. von

    1995-01-01

    Extended tritium experimentation on TFTR has necessitated refurbishing Neutral Beam Long Pulse Ion Sources (LPIS) which developed operational difficulties, both in the TFTR Test Cell and later, in the NB Source Refurbishment Shop. Shipping contaminated sources off-site for repair was not permissible from a transport and safety perspective. Therefore, the NB source repair facility was upgraded by relocating fixtures, tooling, test apparatus, and three-axis coordinate measuring equipment; purchasing and fabricating fume hoods; installing exhaust vents; and providing a controlled negative pressure environment in the source degreaser/decon area. Appropriate air flow monitors, pressure indicators, tritium detectors and safety alarms were also included. The effectiveness of various decontamination methods was explored while the activation was monitored. Procedures and methods were developed to permit complete disassembly and rebuild of an ion source while continuously exhausting the internal volume to the TFTR Stack to avoid concentrations of tritium from outgassing and minimize personnel exposure. This paper presents upgrades made to the LPIS repair facility, various repair tasks performed, and discusses the effectiveness of the decontamination processes utilized

  9. Tritium production in fusion reactors

    International Nuclear Information System (INIS)

    Roth, E.

    1981-08-01

    The present analyses on the possibilities of extracting tritium from the liquid and solid fusion reactor blankets show up many problems. A consistent ensemble of materials and devices for extracting the heat and the tritium has not yet been integrated in a fusion reactor blanket project. The dimensioning of the many pipes required for shifting the tritium can only be done very approximately and the volume taken up by the blanket is difficult to evaluate, etc. The utilization of present data leads to over-dimensioning the installations by prudence and perhaps rejecting the best solutions. In order to measure the parameters of the most promising materials, work must be carried out on well defined samples and not only determine the base physical-chemical coefficients, such as thermal conductivity, scattering coefficients, Sievert parameters, but also the kinetic parameters conventional in chemical engineering, such as the hourly space rates of degassing. It is also necessary to perform long duration experiments under radiation and at operating temperatures, or above, in order to study the ageing of the bodies employed [fr

  10. Tritium calorimeter setup and operation

    International Nuclear Information System (INIS)

    Rodgers, David E.

    2002-01-01

    The LBNL tritium calorimeter is a stable instrument capable of measuring tritium with a sensitivity of 25 Ci. Measurement times range from 8-hr to 7-days depending on the thermal conductivity and mass of the material being measured. The instrument allows accurate tritium measurements without requiring that the sample be opened and subsampled, thus reducing personnel exposure and radioactive waste generation. The sensitivity limit is primarily due to response shifts caused by temperature fluctuation in the water bath. The fluctuations are most likely a combination of insufficient insulation from ambient air and precision limitations in the temperature controller. The sensitivity could probably be reduced to below 5 Ci if the following improvements were made: (1) Extend the external insulation to cover the entire bath and increase the top insulation. (2) Improve the seal between the air space above the bath and the outside air to reduce evaporation. This will limit the response drift as the water level drops. (3) Install an improved temperature controller, preferably with a built in chiller, capable of temperature control to ±0.001 C

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

    International Nuclear Information System (INIS)

    Koran, P.

    1987-01-01

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

  12. A feasibility study on the retrospective evaluation of anomalous local tritium fallout by the analysis of tree rings from selected districts in Austria and Hungary

    International Nuclear Information System (INIS)

    Rank, D.

    1987-01-01

    In May 1974 some of the rain samples collected in the Austrian Alps exhibited unusually high tritium concentrations. The monthly mean values ranged up to 360 Bq/kg (3000 TU) compared with the 20-30 Bq/kg background measured in ''normal'' areas. Tree samples have been collected from the exposed area and rings of 1973, 1974 and 1975 were separated. Cellulose prepared from the wood was combusted and the water samples were analysed for tritium by LSC. The results of measurements show that tritium fallout detected in rainfall was reflected in tree rings: a significant increase of tritium concentration was found in the 1974 rings from the exposed area

  13. Tritium radioluminescent devices, Health and Safety Manual

    Energy Technology Data Exchange (ETDEWEB)

    Traub, R.J.; Jensen, G.A.

    1995-06-01

    This document consolidates available information on the properties of tritium, including its environmental chemistry, its health physics, and safe practices in using tritium-activated RL lighting. It also summarizes relevant government regulations on RL lighting. Chapters are divided into a single-column part, which provides an overview of the topic for readers simply requiring guidance on the safety of tritium RL lighting, and a dual-column part for readers requiring more technical and detailed information.

  14. Overview of light sources powered by tritium

    International Nuclear Information System (INIS)

    Wu Jian; Lei Jiarong; Liu Wenke

    2012-01-01

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

  15. Degradation of elastomers by tritium beta radiation

    International Nuclear Information System (INIS)

    Zapp, P.E.; Tuer, G.L. Jr.

    1984-01-01

    Based on its tritium radiation resistance, ethylene propylene rubber has been selected as a candidate for replacement of nitrile rubber in the SRP tritium facilities. A specification for flange gasket material has been developed for ethylene propylene such that its mechanical properties are similar to those of nitrile rubber. In-process testing of ethylene propylene and nitrile gaskets will be conducted in the tritium facilities under identical exposure conditions

  16. Tritium radioluminescent devices, Health and Safety Manual

    International Nuclear Information System (INIS)

    Traub, R.J.; Jensen, G.A.

    1995-06-01

    This document consolidates available information on the properties of tritium, including its environmental chemistry, its health physics, and safe practices in using tritium-activated RL lighting. It also summarizes relevant government regulations on RL lighting. Chapters are divided into a single-column part, which provides an overview of the topic for readers simply requiring guidance on the safety of tritium RL lighting, and a dual-column part for readers requiring more technical and detailed information

  17. Effluent Treatment Facility tritium emissions monitoring

    International Nuclear Information System (INIS)

    Dunn, D.L.

    1991-01-01

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

  18. The movement of tritium in ecological systems

    International Nuclear Information System (INIS)

    Polevoy, Y; Laichter, Y.

    1988-11-01

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

  19. Tritium monitoring equipments for animal experiment facilities

    International Nuclear Information System (INIS)

    Sato, Hiroo

    1980-01-01

    Animal experiment facilities using tritium are described with reference to laws and regulations concerning radiological safety. Usual breeding facilities and surrounding conditions at non-radioactive animal experiments are summarized on feasible and effective designs of tritium monitors. Characteristics and desirable arrangements of various kinds of tritium monitors such as ionization chambers, proportional counters and liquid scintillation detectors are discussed from the standpoint of monitoring for room, glove-box, stack, liquid waste and personnel. (J.P.N.)

  20. Catalytic membrane reactor for tritium extraction system from He purge

    International Nuclear Information System (INIS)

    Santucci, Alessia; Incelli, Marco; Sansovini, Mirko; Tosti, Silvano

    2016-01-01

    Highlights: • In the HCBB blanket, the produced tritium is recovered by purging with helium; membrane technologies are able to separate tritium from helium. • The paper presents the results of two experimental campaigns. • In the first, a Pd–Ag diffuser for hydrogen separation is tested at several operating conditions. • In the second, the ability of a Pd–Ag membrane reactor for water decontamination is assessed by performing isotopic swamping and water gas shift reactions. - Abstract: In the Helium Cooled Pebble Bed (HCPB) blanket concept, the produced tritium is recovered purging the breeder with helium at low pressure, thus a tritium extraction system (TES) is foreseen to separate the produced tritium (which contains impurities like water) from the helium gas purge. Several R&D activities are running in parallel to experimentally identify most promising TES technologies: particularly, Pd-based membrane reactors (MR) are under investigation because of their large hydrogen selectivity, continuous operation capability, reliability and compactness. The construction and operation under DEMO relevant conditions (that presently foresee a He purge flow rate of about 10,000 Nm 3 /h and a H 2 /He ratio of 0.1%) of a medium scale MR is scheduled for next year, while presently preliminary experiments on a small scale reactor are performed to identify most suitable operative conditions and catalyst materials. This work presents the results of an experimental campaign carried out on a Pd-based membrane aimed at measuring the capability of this device in separating hydrogen from the helium. Many operative conditions have been investigated by considering different He/H 2 feed flow ratios, several lumen pressures and reactor temperatures. Moreover, the performances of a membrane reactor (composed of a Pd–Ag tube having a wall thickness of about 113 μm, length 500 mm and diameter 10 mm) in processing the water contained in the purge gas have been measured by using

  1. Catalytic membrane reactor for tritium extraction system from He purge

    Energy Technology Data Exchange (ETDEWEB)

    Santucci, Alessia, E-mail: alessia.santucci@enea.it [ENEA for EUROfusion, Via E. Fermi 45, 00044 Frascati, Roma (Italy); Incelli, Marco [ENEA for EUROfusion, Via E. Fermi 45, 00044 Frascati, Roma (Italy); DEIM, University of Tuscia, Via del Paradiso 47, 01100 Viterbo (Italy); Sansovini, Mirko; Tosti, Silvano [ENEA for EUROfusion, Via E. Fermi 45, 00044 Frascati, Roma (Italy)

    2016-11-01

    Highlights: • In the HCBB blanket, the produced tritium is recovered by purging with helium; membrane technologies are able to separate tritium from helium. • The paper presents the results of two experimental campaigns. • In the first, a Pd–Ag diffuser for hydrogen separation is tested at several operating conditions. • In the second, the ability of a Pd–Ag membrane reactor for water decontamination is assessed by performing isotopic swamping and water gas shift reactions. - Abstract: In the Helium Cooled Pebble Bed (HCPB) blanket concept, the produced tritium is recovered purging the breeder with helium at low pressure, thus a tritium extraction system (TES) is foreseen to separate the produced tritium (which contains impurities like water) from the helium gas purge. Several R&D activities are running in parallel to experimentally identify most promising TES technologies: particularly, Pd-based membrane reactors (MR) are under investigation because of their large hydrogen selectivity, continuous operation capability, reliability and compactness. The construction and operation under DEMO relevant conditions (that presently foresee a He purge flow rate of about 10,000 Nm{sup 3}/h and a H{sub 2}/He ratio of 0.1%) of a medium scale MR is scheduled for next year, while presently preliminary experiments on a small scale reactor are performed to identify most suitable operative conditions and catalyst materials. This work presents the results of an experimental campaign carried out on a Pd-based membrane aimed at measuring the capability of this device in separating hydrogen from the helium. Many operative conditions have been investigated by considering different He/H{sub 2} feed flow ratios, several lumen pressures and reactor temperatures. Moreover, the performances of a membrane reactor (composed of a Pd–Ag tube having a wall thickness of about 113 μm, length 500 mm and diameter 10 mm) in processing the water contained in the purge gas have been

  2. Tissue-specific incorporation and genotoxicity of different forms of tritium in the marine mussel, Mytilus edulis

    Energy Technology Data Exchange (ETDEWEB)

    Jaeschke, Benedict C., E-mail: ben@ecology.su.s [Ecotoxicology Research and Innovation Centre, School of Biomedical and Biological Sciences, University of Plymouth, Drake Circus, Plymouth PL4 8AA (United Kingdom); Millward, Geoffrey E. [Consolidated Radio-isotope Facility, University of Plymouth, Drake Circus, Plymouth PL4 8AA (United Kingdom); Moody, A. John; Jha, Awadhesh N. [Ecotoxicology Research and Innovation Centre, School of Biomedical and Biological Sciences, University of Plymouth, Drake Circus, Plymouth PL4 8AA (United Kingdom)

    2011-01-15

    Marine mussels (Mytilus edulis) were exposed to seawater spiked with tritiated water (HTO) at a dose rate of 122 and 79 {mu}Gy h{sup -1} for 7 and 14 days, respectively, and tritiated glycine (T-Gly) at a dose rate of 4.9 {mu}Gy h{sup -1} over 7 days. This was followed by depuration in clean seawater for 21 days. Tissues (foot, gills, digestive gland, mantle, adductor muscle and byssus) and DNA extracts from tissues were analysed for their tritium activity concentrations. All tissues demonstrated bio-accumulation of tritium from HTO and T-Gly. Tritium from T-Gly showed increased incorporation into DNA compared to HTO. About 90% of the initial activity from HTO was depurated within one day, whereas T-Gly was depurated relatively slowly, indicating that tritium may be bound with different affinities in tissues. Both forms of tritium caused a significant induction of micronuclei in the haemocytes of mussels. Our findings identify significant differential impacts on Mytilus edulis of the two chemical forms of tritium and emphasise the need for a separate classification and control of releases of tritiated compounds, to adequately protect the marine ecosystem. - Tritium from tritiated glycine demonstrates greater accumulation and persistence in tissues and enhanced genotoxicity in haemocytes of marine mussels, compared to tritium from tritiated water.

  3. Tritium in the environment. NCRP Report No. 62

    International Nuclear Information System (INIS)

    Eisenbud, M.

    1979-01-01

    The NCRP (National Council on Radiation Protection and Measurements) Report No. 62 on tritium is described. Tritium production from various sources, distribution and environmental kinetics, biological behaviour and the dosimetry of tritium are discussed. (author)

  4. Study of column construction and tritium inventory of cryogenic distillation columns for tritium plant of a fusion reactor

    International Nuclear Information System (INIS)

    Iwai, Yasunori; Yamanishi, Toshihiko; Okuno, Kenji

    1996-11-01

    Cryogenic distillation column system is believed to be best for large throughput of hydrogen isotope separation. The major disadvantage of the system is a large tritium inventory in liquid phase. From a viewpoint of safety of a fusion reactor, it is important to establish the design method of minimized the tritium inventory. Anumerical study to investigate the possible design improvement to reduce inventory while maintaining separation performance was conducted. The design conditions are based on ITER DDD report, and details are as follows, 1) Exhaust stream with less than 50 Ci/y loss of tritium, 2) 99.9% purity D2, and 3) 90% purity T2. 4) total inventory with less than 100g. In the design of ITER to process 32 mol/hr, 4 columns (3 of 4 columns make closed loop) are best and total inventory is 94g. Particularly recent design of ITER to process 320 mol/hr requires additional efforts to minimize the inventory. The simulation also suggests it is effective to reduce inventory to draw two different purity product streams. (author)

  5. The introduction of tritium in lactose and saccharose by isotope exchange with gaseous tritium

    International Nuclear Information System (INIS)

    Akulov, G.P.; Snetkova, E.V.; Kaminskij, Yu.L.; Kudelin, B.K.; Efimova, V.L.

    1991-01-01

    Methods for conducting reactions of catalytic protium-tritium isotopic exchange with gaseous tritium were developed in order to synthesize tritium labelled lactose and saccharose. These methods enabled to prepare these labelled disaccharides with high molar activity. The yield was equal to 50-60%, radiochemical purity ∼ 95%

  6. 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.

  7. The p10 gene of Bombyx mori nucleopolyhedrosis virus encodes a ...

    Indian Academy of Sciences (India)

    Department of Microbiology and Cell Biology, Indian Institute of Science, Bangalore 560 012, India. Abstract ..... The P10 sequences were retrievedaextracted from the EMBL bank or from the literature cited. .... of commercial importance.

  8. 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

  9. Process and system for removing tritium

    International Nuclear Information System (INIS)

    Ridgely, J.N.

    1976-01-01

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

  10. Tritium stripping by a catalytic exchange stripper

    International Nuclear Information System (INIS)

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

    1991-01-01

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

  11. Tritium immobilization and packaging using metal hydrides

    International Nuclear Information System (INIS)

    Holtslander, W.J.; Yaraskavitch, J.M.

    1981-04-01

    Tritium recovered from CANDU heavy water reactors will have to be packaged and stored in a safe manner. Tritium will be recovered in the elemental form, T 2 . Metal tritides are effective compounds in which to immobilize the tritium as a stable non-reactive solid with a high tritium capacity. The technology necessary to prepare hydrides of suitable metals, such as titanium and zirconium, have been developed and the properties of the prepared materials evaluated. Conceptual designs of packages for containing metal tritides suitable for transportation and long-term storage have been made and initial testing started. (author)

  12. Development of tritium handing technology(II)

    Energy Technology Data Exchange (ETDEWEB)

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

    2004-02-01

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

  13. 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

  14. 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)

  15. 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

  16. Effects of tritium on electron multiplier performance

    International Nuclear Information System (INIS)

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

    1980-01-01

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

  17. Measurement of tritium concentration in urine

    International Nuclear Information System (INIS)

    Sekiyama, Shigenobu; Deshimaru, Takehide

    1979-01-01

    Concerning the safety management of the advanced thermal reactor ''Fugen'', the internal exposure management for tritium is important, because heavy water is used as the moderator in the reactor, and tritium is produced in the heavy water. Tritium is the radioactive nuclide with the maximum β-ray energy of 18 keV, and the radiation exposure is limited to the internal exposure in human bodies, as tritium is taken in through the skin and by breathing. The tritium concentration in urine of the operators of the Fugen plant was measured. As for tritium measurement, the analysis of raw urine, the analysis after passing through mixed ion exchange resin and the analysis after distillation are applied. The scintillator, the liquid scintillation counter, the ion exchange resin and the distillator are introduced. The preliminary survey was conducted on the urine sample, the scintillator the calibration, etc. The measuring condition, the measurement of efficiency, and the limitation of detection with various background are explained, with the many experimental data and the calculating formula. Concerning the measured tritium concentration in urine, the tritium concentrations in distilled urine, raw urine and the urine refined with ion exchange resin were compared, and the correlation formulae are presented. The actual tritium concentration value in urine was less than 50 pci/ml. The measuring methods of raw urine and the urine refined with ion exchange resin are adequate as they are quick and accurate. (Nakai, Y.)

  18. Ratio of dialytic coefficients of hydrogen and tritium in permeation through palladium alloy film

    International Nuclear Information System (INIS)

    Fujita, Haruyuki; Fujita, Kunio; Sakamoto, Hiroshi; Higashi, Kunio; Okada, Sakae.

    1982-01-01

    The dialytic coefficient for hydrogen is especially large in palladium and its alloys. Recently, with the research on fusion reactors, the dialytic coefficient of tritium permeating through solids and its isotopic effect have been the object of interest. The ratio of the dialytic coefficients of tritium and hydrogen has been usually assumed to be 3. The measurement of the dialytic coefficient in solids using pure tritium is practically difficult. Therefore, the authors carried out the experiment to determine the ratio of the dialytic coefficients of pure T 2 and pure H 2 by permeating the mixed gas of T and H through Pd-Au-Ag alloy. The mixed hydrogen gas was filled in a separation cell containing a palladium alloy tube, and the separation factor of tritium and hydrogen was measured by changing pressure, flow rate and temperature. The separation factor depends mainly on the relative dialytic coefficients of tritium and hydrogen, therefore, the ratio of dialytic coefficients can be determined by the simple analysis of the experimental results. This experimental method is suitable to determine the relative value of dialytic coefficients, and the obtained ratio was about 2.1. (Kako, I.)

  19. Behavior of tritium in the environment. Proceedings series

    Energy Technology Data Exchange (ETDEWEB)

    1979-01-01

    Fifty papers are presented in these proceedings. Individual items are being entered onto the data base. The papers are grouped into seven sections for purposes of continuity. These sections include: distribution of tritium (7 papers); evaluation of future discharges (3 papers); measurement of tritium (3 papers); tritium in the aquatic environment (10 papers); tritium in the terrestrial environment (13 papers); tritium in man (8 papers); and monitoring of tritium (6 papers). (ERB)

  20. Dendritic Cells Primed with Paracoccidioides brasiliensis Peptide P10 Are Therapeutic in Immunosuppressed Mice with Paracoccidioidomycosis

    Directory of Open Access Journals (Sweden)

    Leandro B. R. Silva

    2017-06-01

    Full Text Available Paracoccidioidomycosis (PCM is an endemic systemic mycosis in Latin America, with the highest prevalence in Brazil, Colombia, and Venezuela. Fungi of the Paracoccidioides genus are etiologic agents of the disease. The 15 amino acid peptide P10 is derived from gp43, the main diagnostic antigen of Paracoccidioides brasiliensis. We previously reported that P10-pulsed dendritic cells (DCs induce a protective response against P. brasiliensis. Presently, dexamethasone-treated BALB/c mice were intratracheally infected with P. brasiliensis Pb18 to establish the therapeutic efficacy of P10-pulsed DCs. Immunosuppressed and infected animals that received DCs had a reduction in their fungal burden, and this result was most pronounced in mice receiving DCs primed with P10. The efficacy of therapeutic DCs was significantly augmented by concomitant treatment with trimethoprim-sulfamethoxazole. Additionally, primed-DCs with or without the antifungal drug induced a beneficial Th1-biased immune response and significantly reduced tissue damage. In conclusion, these studies with immunocompromised mice demonstrate that P10-pulsed DCs with or without concomitant antifungal drugs are potently effective in combating invasive PCM. These findings support further translational studies to validate the use of P10-primed DCs for PCM in immunocompetent and immunosuppressed hosts.

  1. Food chain of tritium

    International Nuclear Information System (INIS)

    Kashida, Yoshihiko; Arai, Kiyohiko; Takeda, Hiroshi

    1982-01-01

    Ceratopteris pteriodes, soy bean and aquatic rice were cultivated with HTO, and male rats were administered with the diet containing HTO and T. T metabolism and distribution were determined separately in the free water and the tissue-bound water. T in the free water of the plants showed hardly any changes according to the sites, and that in the dry tissue tended to show high values in the stage and portion of high anabolic activity. In the animal system, the T uptake by the organic components was high, and it was rapidly excreted in tissues with a high metabolic activity, but was low, accompanied by slow excretion, in tissues with a low activity. Therefore, T excreted slowly and remained in the adipose tissue and brain containing large amounts of lipids. As for the T distribution into the tissue components, T was first distributed into small molecules and then, to large molecules after metabolism, in the fraction of hepatic tissue. The in-vivo behaviors of T-labeled compounds were varied because of their in-vivo metabolism. (Chiba, N.)

  2. Determination of tritium by counting; Dosage du tritium par comptage

    Energy Technology Data Exchange (ETDEWEB)

    Schott, R; Froment, G; Pinson, J; Genty, C [Commissariat a l' Energie Atomique, Bruyeres-le-Chatel (France). Centre d' Etudes

    1968-07-01

    Ionisation chamber assay of tritium in any gaseous mixture is a simple, fast and accurate method. We used the method of relative determination by comparison to a standard rather than the method of absolute assay in which case the constants are known with too little accuracy. The efficiency of the chamber was studied in connection to the pressure inside the chamber and its total volume. The calibration is linear in the range we are taking into account (1 to 80 millicuries). The reproducibility of the method is good: 13 runs gave a coefficient of variation of 1.6 per cent. The relative accuracy was found equal to {+-} 1.3 per cent. To end the paper, we describe in detail the apparatus and the ways of proceedings. (authors) [French] Le comptage du tritium par chambre d'ionisation est une methode simple, rapide et precise pour determiner la teneur en tritium d'un melange gazeux quelconque. Nous avons prefere utiliser la methode de determination relative par rapport a un etalon car, dans le cas d'une determination absolue, les constantes sont connues avec une trop grande incertitude. L'efficacite de la chambre a ete etudiee en fonction de la variation de la pression d'argon a l'interieur de la chambre et du volume total, de cette derniere. L'etalonnage s'est revele lineaire dans le domaine de mesures qui nous interessaient (1 a 80 millicuries). La reproductibillte de la methode est tres bonne, le coefficient de variation pour une serie de 13 essais etant de 1,6 pour cent, quant a la precision relative, elle a ete evaluee a {+-} 1,3 pour cent. Pour terminer, nous donnons une description detaillee de l'appareillage utilise et du mode operatoire suivi. (auteurs)

  3. Tritium transport and release from lithium ceramic breeder materials

    International Nuclear Information System (INIS)

    Johnson, C.E.; Kopasz, J.P.; Tam, S.W.

    1994-01-01

    In an operating fusion reactor,, the tritium breeding blanket will reach a condition in which the tritium release rate equals the production rate. The tritium release rate must be fast enough that the tritium inventory in the blanket does not become excessive. Slow tritium release will result in a large tritium inventory, which is unacceptable from both economic and safety viewpoints As a consequence, considerable effort has been devoted to understanding the tritium release mechanism from ceramic breeders and beryllium neutron multipliers through theoretical, laboratory, and in-reactor studies. This information is being applied to the development of models for predicting tritium release for various blanket operating conditions

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

    International Nuclear Information System (INIS)

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

    2008-01-01

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

  5. Development status of the cryogenic distillation system in Cernavoda Tritium Removal Facility

    International Nuclear Information System (INIS)

    Draghia, Mirela; Ana, George; Pasca, Gheorghe; Porcariu, Florina

    2009-01-01

    Full text: The reference design technology for the heavy water detritiation plant of Cernavoda CANDU station is based on combination of Liquid Phase Catalytic Exchange (LPCE) and Cryogenic Distillation (CD) processes. Based on this technology, tritium is transferred from the heavy water to a deuterium stream in the catalyzed isotopic exchange process, LPCE, followed by a final enrichment within the cryogenic distillation cascade. The final step is the tritium storage on metallic hydride. The basic function of the Cryogenic Distillation System (CDS) is the separation of tritium from the tritiated deuterium coming from the LPCE column in the following conditions: - the final product has to be tritium with a concentration of at least 99%; - it must be provided a detritiation factor of at least 100 (the ration between the tritium concentration in the deuterium stream fed to the CD system and the tritium concentration in the returned stream to the LPCE); - the deuterium must be enriched up to 99.995%, by removing the protium; - provisions for safe discharge of the entire inventory of the CD cascade into buffer vessels shall be implemented. To summarize, the present status of the project consists of technical documentation for all the components of CDS, including the P and ID (Pipping and Instrumentation Diagram), preliminary data sheets, technical specifications, drawings for the major components as the buffer vessels, coldbox, etc, and 3D models as well for almost all the components. (authors)

  6. The effective cost of tritium for tokamak fusion power reactors with reduced tritium production systems

    International Nuclear Information System (INIS)

    Gilligan, J.G.; Evans, K.

    1983-01-01

    If sufficient tritium cannot be produced and processed in tokamak blankets then at least two alternatives are possible. Tritium can be purchased; or reactors with reduced tritium (RT) content in the plasma can be designed. The latter choice may require development of magnet technology etc., but the authors show that the impact on the cost-of-electricity may be mild. Cost tradeoffs are compared to the market value of tritium. Adequate tritium production in fusion blankets is preferred, but the authors show there is some flexibility in the deployment of fusion if this is not possible

  7. Tritium sorption on protective coatings for concrete

    International Nuclear Information System (INIS)

    Miller, J.M.; Senohrabek, J.A.; Allsop, P.A.

    1992-11-01

    Because of the high sorption level of tritium on unprotected concrete, a program to examine the effectiveness of various concrete coatings and sealants in reducing tritium sorption was undertaken, and various exposure conditions were examined. Coatings of epoxy, polyurethane, bituminous sealant, bituminous sealant covered with polyvinylidene chloride wrap, alkyd paint, and sodium silicate were investigated with tritium (HTO) vapor concentration, humidity and contact time being varied. An exposure to HT was also carried out, and the effect of humidity on the tritium desorption rate was investigated. The relative effectiveness of the coatings was in the order of bituminous sealant + wrap > bituminous sealant > solvent-based epoxy > 100%-solids epoxy > alkyd paint > sodium silicate. The commercially available coatings for concrete resulted in tritium sorption being reduced to less than 7% of unprotected concrete. This was improved to ∼0.1% with the use of the Saran wrap (polyvinylidene chloride). The amount of tritium sorbed was proportional to tritium concentration. The total tritium sorbed decreased with an increase in humidity. A saturation effect was observed with increasing exposure time for both the coated and unprotected samples. Under the test conditions, complete saturation was not achieved within the maximum 8-hour contact time, except for the solvent-based epoxy. The desorption rate increased with a higher-humidity air purge stream. HT desorbed more rapidly than HTO, but the amount sorbed was smaller. The experimental program showed that HTO sorption by concrete can be significantly reduced with the proper choice of coating. However, tritium sorption on concrete and proposed coatings will continue to be a concern until the effects of the various conditions that affect the adsorption and desorption of tritium are firmly established for both chronic and acute tritium release conditions. Material sorption characteristics must also be considered in

  8. Transfer and incorporation of tritium in mammals

    International Nuclear Information System (INIS)

    Hoek, J. van den; Juan, N.B.

    1979-01-01

    The metabolism of tritium in mammals has been studied in a number of laboratories which have participated in the IAEA Co-ordinated Research Programme on the Behaviour of Tritium in the Environment. The results of these studies are discussed and related to data obtained elsewhere. The animals studied are small laboratory and domestic animals. Tritium has been administered as THO, both in single and long-term dosing experiments, and also as organically bound tritium. The biological half-life of tritium in the body water pool has been determined in different species. The following values have been found: 1.1 days in mice; 13.2 days in kangaroo rats; 3.8 days in pigs; 4.1 days in lactating versus 8.3 in non-lactating goats and 3.1-4.0 days in lactating cows and steers. Much attention has been paid to the incorporation of tritium into organic constituents, both in the animal organism (organs, tissues) and in the secretions of the animal after continuous administration of tritium, mostly as THO. When compared with tritium levels in body water, and expressed as the ratio of specific activities, values of 0.25 and 0.40 have been found in mice liver and testis respectively. In cow's milk, these ratios vary from 0.30 for casein to 0.60 for lactose. The transfer of tritium into milk after continuous ingestion of THO by a lactating cow is about 1.50% of the daily ingested tritium per litre of milk. Some results of experiments, utilizing organically bound tritium, are also presented. (author)

  9. Tritium retention in S-65 beryllium after 100 eV plasma exposure

    Energy Technology Data Exchange (ETDEWEB)

    Causey, R.A. [Sandia National Labs., Livermore, CA (United States); Longhurst, G.R. [Idaho National Engineering Laboratories, Idaho Falls, 83415 (United States); Harbin, W. [Los Alamos National Laboratories, Los Alamos, NM 87545 (United States)

    1997-02-01

    The tritium plasma experiment (TPE) has been used to measure the retention of tritium in S-65 beryllium under conditions similar to that expected for the international thermonuclear experimental reactor (ITER). Beryllium samples 2 mm thick and 50 mm in diameter were exposed to a plasma of tritium and deuterium. The particle flux striking the samples was varied from approximately 1 x 10{sup 17} (D+T)/cm{sup 2} s up to about 3 x 10{sup 18} (D+T)/cm{sup 2} s. The beryllium samples were negatively biased to elevate the energy of the impinging ions to 100 eV. The temperature of the samples was varied from 373 K to 973 K. Exposure times of 1 h were used. Subsequent to the plasma exposure, the samples were outgassed in a separate system where 99% He and 1% H{sub 2} gas was swept over the samples during heating. The sweep gas along with the released tritium was sent through an ionization chamber, through a copper oxide catalyst bed, and into a series of glycol bubblers. The amount of released tritium was determined both by the ionization chamber and by liquid scintillation counting of the glycol. Tritium retention in the beryllium disks varied from a high of 2.4 x 10{sup 17} (D+T)/cm{sup 2} at 373 K to a low of 1 x 10{sup 16} (D+T)/cm{sup 2} at 573 K. For almost every case, the tritium retention in the beryllium was less than that calculated using the C=0 boundary condition at the plasma facing surface. It is believed that this lower than expected retention is due to rapid release of tritium from the large specific surface area created in the implant zone due to the production of voids, bubbles, and blisters. (orig.).

  10. Tritium retention in S-65 beryllium after 100 eV plasma exposure

    Science.gov (United States)

    Causey, Rion A.; Longhurst, Glen R.; Harbin, Wally

    1997-02-01

    The tritium plasma experiment (TPE) has been used to measure the retention of tritium in S-65 beryllium under conditions similar to that expected for the international thermonuclear experimental reactor (ITER). Beryllium samples 2 mm thick and 50 mm in diameter were exposed to a plasma of tritium and deuterium. The particle flux striking the samples was varied from approximately 1 × 10 17 ( D + T)/ cm2s up to about 3 × 10 18 ( D + T)/ cm2s. The beryllium samples were negatively biased to elevate the energy of the impinging ions to 100 eV. The temperature of the samples was varied from 373 K to 973 K. Exposure times of 1 h were used. Subsequent to the plasma exposure, the samples were outgassed in a separate system where 99% He and 1% H 2 gas was swept over the samples during heating. The sweep gas along with the released tritium was sent through an ionization chamber, through a copper oxide catalyst bed, and into a series of glycol bubblers. The amount of released tritium was determined both by the ionization chamber and by liquid scintillation counting of the glycol. Tritium retention in the beryllium disks varied from a high of 2.4 × 10 17 ( D + T)/ cm2 at 373 K to a low of 1 × 10 16 ( D + T)/ cm2 at 573 K. For almost every case, the tritium retention in the beryllium was less than that calculated using the C = 0 boundary condition at the plasma facing surface. It is believed that this lower than expected retention is due to rapid release of tritium from the large specific surface area created in the implant zone due to the production of voids, bubbles, and blisters.

  11. 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.

  12. Conceptual design on interface between ITER and tritium extraction system of Chinese helium-cooled solid breeder test blanket module

    International Nuclear Information System (INIS)

    Zhang Long; Luo Tianyong; Feng Kaiming

    2010-01-01

    Tritium extraction system is essential for CN HCSB TBM for safety and technical reasons. Based on the assessments of system functions, integration issues and safety considerations, two main modifications of the system from previous design (Feng et al., 2007 ; Chen et al., 2008 ) are adopted: a)the TES has been split to 2 parts with one in port cell and another in tritium building. Q 2 O in the purge gas is reduced to Q 2 in a hot metal bed located in port cell; Q 2 is separated from the stream by a pair of cryogenic molecular sieve beds and a Pd/Ag diffuser located in tritium building. b)isotope separation process has been excluded. TES components sizes are estimated and space allocations are estimated. Required services and where and when they are needed are preliminary defined. Fluids delivered towards ITER tritium system are analyzed.

  13. 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)

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

    International Nuclear Information System (INIS)

    Diabate, S.; Strack, S.

    1990-12-01

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

  15. Incorporation of organically bound tritium (OBT) of food or tritium (OBT) of food or tritiated water (TW) into foetuses, placentas and some tissues of pregnant rat

    International Nuclear Information System (INIS)

    Rochalska, M.; Szot, Z.

    1978-01-01

    Pregnant rats between 9 and 17 days of gestation were given OBT or TW during 5 days. On the 6th day the animals were sacrificed (13, 15, 17, 19 and 21st day gestation). Tritium radioactivity of foetuses, placentas, yolk sacs, some organs of mother and some organic compounds separated from foetuses and placentas were examined. The results were referred to the last day of experiment. The highest tritium concentration in the foetuses and placentas was found on the 13th day of gestation and decreased until the 17th day. Then, after a short lasting increase, the incorporation values attained the lowest values on the 21st day. Tritium radioactivity of foetuses was of the order of magnitude of that in the mother's liver and small intestine. During the last days of pregnancy diminished incorporation into phospholipids, nucleic acids and proteins and an increase into acid-soluble fraction was observed. (author)

  16. A new tritium process monitor based on scintillating fibres

    International Nuclear Information System (INIS)

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

    1998-01-01

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

  17. A review of tritium licensing requirements

    International Nuclear Information System (INIS)

    Meikle, A.B.

    1982-12-01

    Present Canadian regulations and anticipated changes to these regulations relevant to the utilization of tritium in fusion facilities and in commercial applications have been reviewed. It is concluded that there are no serious licensing obstacles, but there are a number of requirements which must be met. A license will be required from Atomic Energy Control Board if Ontario Hydro tritium is to be applied by other users. A license is required from the Federal Government to export or import tritium. A licensed container will be required for the storage and shipping of tritium. The containers being designed by AECL and Ontario Hydro and which are currently being tested will adequately store and ship all of the Ontario Hydro tritium but are unnecessarily large for the small quantities required by the commercial tritium users. Also, some users may prefer to receive tritium in gaseous form. An additional, smaller container should be considered. The licensing of overseas fusion facilities for the use of tritium is seen as a major undertaking offering opportunities to Canadian Fusion Fuels Technology Project to undertake health, safety and environmental analysis on behalf of these facilities

  18. Immobilization and packaging of recovered tritium

    International Nuclear Information System (INIS)

    Holtslander, W.J.; Miller, J.M.

    1982-09-01

    The evaluation of metal hydrides as a medium for immobilization of tritium is reviewed. The work demonstrated methods of preparation and examined the properties of titanium and zirconium hydride for this application. Methods of packaging the metal hydrides for transportation and recoverable storage of tritium were also examined

  19. A study of electrolytic tritium production

    International Nuclear Information System (INIS)

    Storms, E.K.; Talcott, C.L.

    1990-01-01

    Tritium production is being investigated using cathodes made from palladium and its alloys with various surface treatments. Three anode materials have been studied as well as different impurities in the electrolyte. Tritium has been produced in about 10% of the cells studied but there is, as yet, no pattern of behavior that would make the effect predictable. 15 refs., 4 figs., 6 tabs

  20. Enantiospecific tritium labeling of 28-homocastasterone

    Czech Academy of Sciences Publication Activity Database

    Elbert, Tomáš; Patil, Mahadeo Rajshekhar; Marek, Aleš

    2017-01-01

    Roč. 60, č. 3 (2017), s. 176-182 ISSN 0362-4803 R&D Projects: GA AV ČR IAA400550801 Institutional support: RVO:61388963 Keywords : 28-homocastasterone * brassinosteroids * enantiospecific reaction * tritium dehalogenation * tritium labeling Subject RIV: CC - Organic Chemistry OBOR OECD: Organic chemistry Impact factor: 1.745, year: 2016

  1. Synthesis of tritium-labeled fosfomycin

    International Nuclear Information System (INIS)

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

    1982-01-01

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

  2. Tritium waste disposal technology in the US

    International Nuclear Information System (INIS)

    Albenesius, E.L.; Towler, O.A.

    1983-01-01

    Tritium waste disposal methods in the US range from disposal of low specific activity waste along with other low-level waste in shallow land burial facilities, to disposal of kilocurie amounts in specially designed triple containers in 65' deep augered holes located in an aird region of the US. Total estimated curies disposed of are 500,000 in commercial burial sites and 10 million curies in defense related sites. At three disposal sites in humid areas, tritium has migrated into the ground water, and at one arid site tritium vapor has been detected emerging from the soil above the disposal area. Leaching tests on tritium containing waste show that tritium in the form of HTO leaches readily from most waste forms, but that leaching rates of tritiated water into polymer impregnated concrete are reduced by as much as a factor of ten. Tests on improved tritium containment are ongoing. Disposal costs for tritium waste are 7 to 10 dollars per cubic foot for shallow land burial of low specific activity tritium waste, and 10 to 20 dollars per cubic foot for disposal of high specific activity waste. The cost of packaging the high specific activity waste is 150 to 300 dollars per cubic foot. 18 references

  3. Achieving mask order processing automation, interoperability and standardization based on P10

    Science.gov (United States)

    Rodriguez, B.; Filies, O.; Sadran, D.; Tissier, Michel; Albin, D.; Stavroulakis, S.; Voyiatzis, E.

    2007-02-01

    Last year the MUSCLE (Masks through User's Supply Chain: Leadership by Excellence) project was presented. Here is the project advancement. A key process in mask supply chain management is the exchange of technical information for ordering masks. This process is large, complex, company specific and error prone, and leads to longer cycle times and higher costs due to missing or wrong inputs. Its automation and standardization could produce significant benefits. We need to agree on the standard for mandatory and optional parameters, and also a common way to describe parameters when ordering. A system was created to improve the performance in terms of Key Performance Indicators (KPIs) such as cycle time and cost of production. This tool allows us to evaluate and measure the effect of factors, as well as the effect of implementing the improvements of the complete project. Next, a benchmark study and a gap analysis were performed. These studies show the feasibility of standardization, as there is a large overlap in requirements. We see that the SEMI P10 standard needs enhancements. A format supporting the standard is required, and XML offers the ability to describe P10 in a flexible way. Beyond using XML for P10, the semantics of the mask order should also be addressed. A system design and requirements for a reference implementation for a P10 based management system are presented, covering a mechanism for the evolution and for version management and a design for P10 editing and data validation.

  4. HAT-P-10b: A LIGHT AND MODERATELY HOT JUPITER TRANSITING A K DWARF

    International Nuclear Information System (INIS)

    Bakos, G. A.; Pal, A.; Torres, G.; Sipocz, B.; Latham, D. W.; Noyes, R. W.; Hartman, J.; Esquerdo, G. A.; Sasselov, D. D.; Kovacs, Gabor; Stefanik, R. P.; Kovacs, Geza; Fischer, D. A.; Johnson, J. A.; Marcy, G. W.; Howard, A. W.; Butler, R. P.; Lazar, J.; Papp, I.; Sari, P.

    2009-01-01

    We report on the discovery of HAT-P-10b, one of the lowest mass (0.487 ± 0.018 M J ) transiting extrasolar planets (TEPs) discovered to date by transit searches. HAT-P-10b orbits the moderately bright V = 11.89 K dwarf GSC 02340-01714, with a period P = 3.7224747 ± 0.0000065 days, transit epoch T c = 2454759.68683 ± 0.00016 (BJD), and duration 0.1090 ± 0.0008 days. HAT-P-10b has a radius of 1.005 +0.032 -0.027 R J yielding a mean density of 0.594 ± 0.052 g cm -3 . Comparing these observations with recent theoretical models we find that HAT-P-10b is consistent with a ∼4.5 Gyr, almost pure hydrogen and helium gas giant planet with a 10 M + core. With an equilibrium temperature of T eq = 1020 ± 17 K, HAT-P-10b is one of the coldest TEPs. Curiously, its Safronov number θ = 0.053 ± 0.002 falls close to the dividing line between the two suggested TEP populations.

  5. Tritium labeling of detonation nanodiamonds.

    Science.gov (United States)

    Girard, Hugues A; El-Kharbachi, Abdelouahab; Garcia-Argote, Sébastien; Petit, Tristan; Bergonzo, Philippe; Rousseau, Bernard; Arnault, Jean-Charles

    2014-03-18

    For the first time, the radioactive labeling of detonation nanodiamonds was efficiently achieved using a tritium microwave plasma. According to our measurements, the total radioactivity reaches 9120 ± 120 μCi mg(-1), with 93% of (3)H atoms tightly bonded to the surface and up to 7% embedded into the diamond core. Such (3)H doping will ensure highly stable radiolabeled nanodiamonds, on which surface functionalization is still allowed. This breakthrough opens the way to biodistribution and pharmacokinetics studies of nanodiamonds, while this approach can be scalable to easily treat bulk quantities of nanodiamonds at low cost.

  6. Tritium separation techniques in nuclear fusion reactor system

    International Nuclear Information System (INIS)

    Naruse, Yuji

    1982-01-01

    Thermal diffusion process, liquefying distillation method, gaseous diffusion method, metallic film permeation method, chemical exchange method and water distillation method are described, with respect to the present state of development and the problems to be solved. (J.P.N.)

  7. Separation of tritium from heavy water by vacuum distillation

    International Nuclear Information System (INIS)

    Vidal, M.I.; Cabrera, C.A.

    1996-01-01

    In this report the feasibility of using vacuum distillation to detriate the moderator of a HWR nuclear power plant is studied. It is intended to use, for this purpose, the Atucha I nuclear power plant present facilities. The physical-chemistry of the system is described and the most appropriate range of operating conditions is examined. The availability of data to make use of the present equipment is also analyzed. (author). 20 refs., 3 figs., 1 tab

  8. Experiences with decontaminating tritium-handling apparatus

    International Nuclear Information System (INIS)

    Maienschein, J.L.; Garcia, F.; Garza, R.G.; Kanna, R.L.; Mayhugh, S.R.; Taylor, D.T.

    1992-01-01

    Tritium-handling apparatus has been decontaminated as part of the downsizing of the LLNL Tritium Facility. Two stainless-steel glove boxes that had been used to process lithium deuteride-tritide (LiDT) slat were decontaminated using the Portable Cleanup System so that they could be flushed with room air through the facility ventilation system. In this paper the details on the decontamination operation are provided. A series of metal (palladium and vanadium) hydride storage beds have been drained of tritium and flushed with deuterium, in order to remove as much tritium as possible. The bed draining and flushing procedure is described, and a calculational method is presented which allows estimation of the tritium remaining in a bed after it has been drained and flushed. Data on specific bed draining and flushing are given

  9. Uptake of atmospheric tritium by market foods

    International Nuclear Information System (INIS)

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

    1992-01-01

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

  10. Disposal of tritium-exposed metal hydrides

    International Nuclear Information System (INIS)

    Nobile, A.; Motyka, T.

    1991-01-01

    A plan has been established for disposal of tritium-exposed metal hydrides used in Savannah River Site (SRS) tritium production or Materials Test Facility (MTF) R ampersand D operations. The recommended plan assumes that the first tritium-exposed metal hydrides will be disposed of after startup of the Solid Waste Disposal Facility (SWDF) Expansion Project in 1992, and thus the plan is consistent with the new disposal requiremkents that will be in effect for the SWDF Expansion Project. Process beds containing tritium-exposed metal hydride powder will be disposed of without removal of the powder from the bed; however, disposal of tritium-exposed metal hydride powder that has been removed from its process vessel is also addressed

  11. DOE handbook: Tritium handling and safe storage

    International Nuclear Information System (INIS)

    1999-03-01

    The DOE Handbook was developed as an educational supplement and reference for operations and maintenance personnel. Most of the tritium publications are written from a radiological protection perspective. This handbook provides more extensive guidance and advice on the null range of tritium operations. This handbook can be used by personnel involved in the full range of tritium handling from receipt to ultimate disposal. Compliance issues are addressed at each stage of handling. This handbook can also be used as a reference for those individuals involved in real time determination of bounding doses resulting from inadvertent tritium releases. This handbook provides useful information for establishing processes and procedures for the receipt, storage, assay, handling, packaging, and shipping of tritium and tritiated wastes. It includes discussions and advice on compliance-based issues and adds insight to those areas that currently possess unclear DOE guidance

  12. Diurnal variations of tritium uptake by plants

    International Nuclear Information System (INIS)

    Hettinger, M.; Diabate, S.; Strack, S.

    1991-02-01

    The influence of the diurnal cycle is important for the behaviour of environmental tritium in the vegetation. A mathematical model has been used to calculate the deposition of tritium in plants as a function of diurnal variations of climatic parameters. The necessary physiological parameters (relationship of net photosynthesis and growth) were derived from growth experiments for tomatoes and maize. In chamber experiments, tomato and maize plants were exposed to tritium with natural diurnal variations of the climatic conditions. Within the range of standard deviations the measured concentrations of tritium in tissue free water of tomatoes correspond well to the estimated values. Furthermore, the incorporation into non-exchangeable organically bound tritium (OBT nx) can be sufficiently modelled and explained. There are deviations from the estimated concentrations in some parts of maize leaves. (orig.) [de

  13. DOE handbook: Tritium handling and safe storage

    Energy Technology Data Exchange (ETDEWEB)

    NONE

    1999-03-01

    The DOE Handbook was developed as an educational supplement and reference for operations and maintenance personnel. Most of the tritium publications are written from a radiological protection perspective. This handbook provides more extensive guidance and advice on the null range of tritium operations. This handbook can be used by personnel involved in the full range of tritium handling from receipt to ultimate disposal. Compliance issues are addressed at each stage of handling. This handbook can also be used as a reference for those individuals involved in real time determination of bounding doses resulting from inadvertent tritium releases. This handbook provides useful information for establishing processes and procedures for the receipt, storage, assay, handling, packaging, and shipping of tritium and tritiated wastes. It includes discussions and advice on compliance-based issues and adds insight to those areas that currently possess unclear DOE guidance.

  14. Tritium issues in commercial pressurized water reactors

    International Nuclear Information System (INIS)

    Jones, G.

    2008-01-01

    Tritium has become an important radionuclide in commercial Pressurized Water Reactors because of its mobility and tendency to concentrate in plant systems as tritiated water during the recycling of reactor coolant. Small quantities of tritium are released in routine regulated effluents as liquid water and as water vapor. Tritium has become a focus of attention at commercial nuclear power plants in recent years due to inadvertent, low-level, chronic releases arising from routine maintenance operations and from component failures. Tritium has been observed in groundwater in the vicinity of stations. The nuclear industry has undertaken strong proactive corrective measures to prevent recurrence, and continues to eliminate emission sources through its singular focus on public safety and environmental stewardship. This paper will discuss: production mechanisms for tritium, transport mechanisms from the reactor through plant, systems to the environment, examples of routine effluent releases, offsite doses, basic groundwater transport and geological issues, and recent nuclear industry environmental and legal ramifications. (authors)

  15. The organic tritium in the environment

    International Nuclear Information System (INIS)

    Kirchmann, R.

    1979-01-01

    Sources, organization process, and biological availability of organic tritium released in the environment, transfer of organic tritium in the environment from methane or soil to plants and from food to mammals, transfer of tritium in aquatic ecosystems, and dose to man resulting of the ingestion of tritiated food were reviewed and discussed. Some data about transfer of organic tritium in terrestrial and aquatic ecosystems reported by literatures were summarized and were supplied with recent data on biological accumulation of organic tritium in the food chain. It was stressed that more research must be done in future because data available were still insufficient. Last, some research programs in progress or planned were stated. (Tsunoda, M.)

  16. Recent environmental tritium levels in Japan

    International Nuclear Information System (INIS)

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

    1982-01-01

    Data of the tritium surveillance program are summarized for the period of 1967 through 1980. Samples of surface water, tap water, coastal sea water and ground water were collected from environs of commercial nuclear power plants and nuclear facilities, and were analyzed by liquid scintillation counting. Although the results show some differences in tritium concentrations in water samples from various part of the country, there is a general tendency of the concentration in surface waters to decline as a function of time. This implies that environmental waters in Japan generally have not been influenced by the discharged effluents of the facilities or the stations with regard to tritium contamination and that the tritium content of precipitation still plays the dominant role in reflecting annual variation of tritium concentration in surface waters. (J.P.N.)

  17. Consideration for a tritium removal facility at the Cernavoda Nuclear Power Station

    International Nuclear Information System (INIS)

    2006-01-01

    Full text: A pre-feasibility study considering process options for a Tritium Removal Facility at the Cernavoda Nuclear Power Station has been completed by ICIT and AECL. Three different process options were considered. These three options differ in the front-end process used to transfer tritium from heavy water to deuterium gas. All three options use cryogenic distillation (CD) as a back end process to extract tritium from the deuterium gas stream and concentrate it into a small volume stream of pure DT or T 2 that can be immobilized on a titanium sponge. The first option for the front-end process is Liquid Phase Catalytic Exchange (LPCE). The LPCE column is used to transfer the tritium from the heavy water to a recirculating stream of deuterium gas. The separation of hydrogen isotopes takes place in the cryogenic distillation column. Tritium-depleted deuterium gas from the CD system is fed back to the LPCE column. The cryogenic distillation system concentrates the tritium into a small volume of elemental tritium for storage. Tritiated heavy water that has been purified to remove catalyst poisons is fed to the top of the LPCE column. The heavy water leaving the column is depleted in deuterium. Both existing detritiation plants built to detritiate CANDU reactors (the Darlington TRF in Canada and the Wolsung TRF in Korea) use variations of the LPCE-CD process. The second option uses electrolysis to convert tritiated heavy water into oxygen and tritiated deuterium gas. The deuterium gas is sent to the Cryogenic Distillation system to extract and concentrate the tritium. The tritium depleted deuterium gas is recombined with the electrolytic oxygen to give a tritium-depleted heavy water product. The third option uses a Combined Electrolysis and Catalytic Exchange (CECE) front end. A CECE process concentrates the tritium in the water and, using water electrolysis, converts the concentrated tritium into deuterium gas. An overhead catalytic recombiner converts the

  18. Tritium decay helium-3 effects in tungsten

    Directory of Open Access Journals (Sweden)

    M. Shimada

    2017-08-01

    Full Text Available Tritium (T implanted by plasmas diffuses into bulk material, especially rapidly at elevated temperatures, and becomes trapped in neutron radiation-induced defects in materials that act as trapping sites for the tritium. The trapped tritium atoms will decay to produce helium-3 (3He atoms at a half-life of 12.3 years. 3He has a large cross section for absorbing thermal neutrons, which after absorbing a neutron produces hydrogen (H and tritium ions with a combined kinetic energy of 0.76 MeV through the 3He(n,HT nuclear reaction. The purpose of this paper is to quantify the 3He produced in tungsten by tritium decay compared to the neutron-induced helium-4 (4He produced in tungsten. This is important given the fact that helium in materials not only creates microstructural damage in the bulk of the material but alters surface morphology of the material effecting plasma-surface interaction process (e.g. material evolution, erosion and tritium behavior of plasma-facing component materials. Effects of tritium decay 3He in tungsten are investigated here with a simple model that predicts quantity of 3He produced in a fusion DEMO FW based on a neutron energy spectrum found in literature. This study reveals that: (1 helium-3 concentration was equilibrated to ∼6% of initial/trapped tritium concentration, (2 tritium concentration remained approximately constant (94% of initial tritium concentration, and (3 displacement damage from 3He(n,HT nuclear reaction became >1 dpa/year in DEMO FW.

  19. Tritium behavior in an aquatic ecosystem

    International Nuclear Information System (INIS)

    Komatsu, K.

    1982-01-01

    Tritium behavior in aquatic organisms through a model food chain was investigated. In this model food chain, tritium in water reaches bacteria or Japanese killifish via diatoms and brine shrimps. Tritium accumulation in these organisms as organic bound form was expressed as the R value which is defined as the ratio of tritium specific activity in lyophilized organisms (μCi/gH) to that in water (μCi/gH). The maximum R values were 0.5 in diatoms: Chaetoceros gracilis, 0.2 in bacteria: Escherichia coli, 0.5 in brine shrimps: Artemia salina, and 0.32 in Japanese killifish: Oryzias latipes under the growing condition in which tritium accumulation was due to tritium in tritiated water and not tritiated foods. Brine shrimps and Japanese killifish were grown from larve to adult in tritiated sea water and were fed on tritiated foods (model food chain). Their R values were 0.70 and 0.67, respectively. Bacteria, which grew in tritiated water by adding the hydrolysate of tritiated brine shrimps, showed a maximum R value at 0.32. The R values of each organ of Japanese killifish and of DNA and the nucleotides purified from brine shrimps growing in tritiated water with or without tritiated food were measured to estimate the tritium distribution in the body or various molecules of the organisms. These results did not indicate concentration of tritium in specific organs or compounds. The changes of specific activity of tritium in these organisms were measured when they were transferred to non-tritiated water. These retention of tritium was not only different among the tissues but also depended on whether or not the organisms were reared with tritiated foods. (author)

  20. Issues Associated with Tritium Legacy Materials

    International Nuclear Information System (INIS)

    Mills, Michael

    2008-01-01

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

  1. PDRD (SR13046) TRITIUM PRODUCTION FINAL REPORT

    Energy Technology Data Exchange (ETDEWEB)

    Smith, P.; Sheetz, S.

    2013-09-30

    Utilizing the results of Texas A&M University (TAMU) senior design projects on tritium production in four different small modular reactors (SMR), the Savannah River National Laboratory’s (SRNL) developed an optimization model evaluating tritium production versus uranium utilization under a FY2013 plant directed research development (PDRD) project. The model is a tool that can evaluate varying scenarios and various reactor designs to maximize the production of tritium per unit of unobligated United States (US) origin uranium that is in limited supply. The primary module in the model compares the consumption of uranium for various production reactors against the base case of Watts Bar I running a nominal load of 1,696 tritium producing burnable absorber rods (TPBARs) with an average refueling of 41,000 kg low enriched uranium (LEU) on an 18 month cycle. After inputting an initial year, starting inventory of unobligated uranium and tritium production forecast, the model will compare and contrast the depletion rate of the LEU between the entered alternatives. This is an annual tritium production rate of approximately 0.059 grams of tritium per kilogram of LEU (g-T/kg-LEU). To date, the Nuclear Regulatory Commission (NRC) license has not been amended to accept a full load of TPBARs so the nominal tritium production has not yet been achieved. The alternatives currently loaded into the model include the three light water SMRs evaluated in TAMU senior projects including, mPower, Holtec and NuScale designs. Initial evaluations of tritium production in light water reactor (LWR) based SMRs using optimized loads TPBARs is on the order 0.02-0.06 grams of tritium per kilogram of LEU used. The TAMU students also chose to model tritium production in the GE-Hitachi SPRISM, a pooltype sodium fast reactor (SFR) utilizing a modified TPBAR type target. The team was unable to complete their project so no data is available. In order to include results from a fast reactor, the SRNL

  2. Advanced Separations at SRS

    International Nuclear Information System (INIS)

    Thompson, M.C.

    1998-03-01

    The Savannah River Site (SRS) has many waste streams which are contaminated with radionuclides and/or hazardous materials which must be treated to remove the radioactivity (Cs, Sr, tritium, actinides) and hazardous components (polychlorinated biphenyls, cyanide, metal ions). This task provides test beds for ESP-developed separations materials and technologies using actual SRS waste streams. The work includes different SRS waste streams; high level waste solutions presently stored in underground tanks onsite, water recycled from the waste vitrification plant, and reactor basin water in excess facilities

  3. Tritium-related materials problems in fusion reactors

    International Nuclear Information System (INIS)

    Hickman, R.G.

    1976-01-01

    Pressing materials problems that must be solved before tritium can be used to produce energy economically in fusion reactors are discussed. The following topics are discussed: (1) breeding tritium, (2) recovering bred tritium, (3) containing tritium, (4) fuel recycling, and (5) laser-fusion fueling

  4. Optimization of tritium management within the ITER project

    International Nuclear Information System (INIS)

    Cortes, P.; Elbez-Uzan, J.; Glugla, M.; Rosanvallon, S.; Ciattaglia, S.; Iseli, M.; Rodriguez-Rodrigo, L.

    2009-01-01

    The authors describe the tritium cycle existing within the ITER project and which has been considered since its beginning. They indicate how confinement systems ensure tritium confinement, how tritium is recovered and processed. They indicate the different tritium management optimization ways which have been identified and integrated into the ITER design

  5. 10 CFR 39.55 - Tritium neutron generator target sources.

    Science.gov (United States)

    2010-01-01

    ... 10 Energy 1 2010-01-01 2010-01-01 false Tritium neutron generator target sources. 39.55 Section 39... Equipment § 39.55 Tritium neutron generator target sources. (a) Use of a tritium neutron generator target....77. (b) Use of a tritium neutron generator target source, containing quantities exceeding 1,110 GBg...

  6. Tritium module for ITER/Tiber system code

    International Nuclear Information System (INIS)

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

    1988-01-01

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

  7. A new box system for a high pressure tritium pump

    International Nuclear Information System (INIS)

    Wilson, S.W.; Borree, R.J.; Chambers, D.I.; Souers, P.C.; Merrill, J.T.; Wiggins, R.K.

    1988-01-01

    A 200 MPa (30 kpsi) high pressure tritium pump inside a box system is described. This system is currently under construction but all representative mechanical parts have been fabricated and tested. The pump is a conventional mechanical-plus-cryostaged system, so that most of the interesting features are in the box. The system contains nine separate sections, with automatic pressure balancing and venting systems. Five sections are hood-to-box convertible enclosures with inflatable door seals. The procedure of cryostaging with liquid argon is described. Special detail is given to valves and motor shaft seals. 3 refs., 4 figs

  8. Incorporation and metabolism of tritium in pregnant mice and their offspring after feeding organically labelled tritiated milk powder during pregnancy

    International Nuclear Information System (INIS)

    Bruwaene, R. van; Gerber, G.B.; Kirchmann, R.; Maes, J.; Fagniart, E.

    1982-01-01

    Food mixed from equal amounts of organically labelled tritiated milk powder and normal food pellets was given to mice during pregnancy and lactation. At birth, some new-born were swapped with those from non-exposed mothers to compare separately accumulation and metabolism during pregnancy and lactation. Young mice were sacrificed at different time after birth, and tritium activity in different organs was determined. Tritium activity was also determined in maternal organs at various times during and after the 42 days feeding period. The activity per g in some tissues of the young, particularly in fat, exceeded that of the food given, probably as a result of the high activity and low metabolic dilution of the fats in the food. Young mice contaminated during lactation and pregnancy contained still detectible activity at an age of 2 months. Activity was nearly the same in mice receiving tritium only during lactation as in those receiving it also during pregnancy. Dilution was more marked due to rapid growth when tritium application was discontinued at birth. Tritium water was replaced most rapidly, organic tritium in brain turned over most slowly with and additional metabolic component of a half life in the order of 1 month. Organic tritium in liver displayed an intermediate half life. (author)

  9. Tritium Decay Helium-3 Effects in Tungsten

    Energy Technology Data Exchange (ETDEWEB)

    Shimada, M. [Idaho National Lab. (INL), Idaho Falls, ID (United States); Merrill, B. J. [Idaho National Lab. (INL), Idaho Falls, ID (United States)

    2016-06-01

    A critical challenge for long-term operation of ITER and beyond to a Demonstration reactor (DEMO) and future fusion reactor will be the development of plasma-facing components (PFCs) that demonstrate erosion resistance to steady-state/transient heat fluxes and intense neutral/ion particle fluxes under the extreme fusion nuclear environment, while at the same time minimizing in-vessel tritium inventories and permeation fluxes into the PFC’s coolant. Tritium will diffuse in bulk tungsten at elevated temperatures, and can be trapped in radiation-induced trap site (up to 1 at. % T/W) in tungsten [1,2]. Tritium decay into helium-3 may also play a major role in microstructural evolution (e.g. helium embrittlement) in tungsten due to relatively low helium-4 production (e.g. He/dpa ratio of 0.4-0.7 appm [3]) in tungsten. Tritium-decay helium-3 effect on tungsten is hardly understood, and its database is very limited. Two tungsten samples (99.99 at. % purity from A.L.M.T. Co., Japan) were exposed to high flux (ion flux of 1.0x1022 m-2s-1 and ion fluence of 1.0x1026 m-2) 0.5%T2/D2 plasma at two different temperatures (200, and 500°C) in Tritium Plasma Experiment (TPE) at Idaho National Laboratory. Tritium implanted samples were stored at ambient temperature in air for more than 3 years to investigate tritium decay helium-3 effect in tungsten. The tritium distributions on plasma-exposed was monitored by a tritium imaging plate technique during storage period [4]. Thermal desorption spectroscopy was performed with a ramp rate of 10°C/min up to 900°C to outgas residual deuterium and tritium but keep helium-3 in tungsten. These helium-3 implanted samples were exposed to deuterium plasma in TPE to investigate helium-3 effect on deuterium behavior in tungsten. The results show that tritium surface concentration in 200°C sample decreased to 30 %, but tritium surface concentration in 500°C sample did not alter over the 3 years storage period, indicating possible tritium

  10. 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.))

  11. Transfer of fallout tritium from environment to human body

    International Nuclear Information System (INIS)

    Hisamatsu, Shun-ichi; Takizawa, Yukio

    1989-01-01

    A large quntity of tritium will be used as a fuel of nuclear fusion in the future. It is, therefore, considered important to elucidate tritium behavior present in the environment and the process of tritium transfer from the environment to the human body. Fallout tritium is an applicable material in searching for the long term behavior of tritium in the environment. This paper focuses on the American, Italian, Japanese literature concerning fallout tritium in food and in the human body. The specific activity ratio of bound to free tritium poses an important problem. The mechanism of biological concentration must await further studies. (N.K.) 63 refs

  12. Tritium distributing in stainless steel determined by chemical etchin

    International Nuclear Information System (INIS)

    Xiong Yifu; Luo Deli; Chen Changan; Chen Shicun; Jing Wenyong

    2009-01-01

    The depth distribution of tritium in stainless steel was measured by chemical etching. The results show that the method can more quantitatively evaluate the tritium distributing in stainless steel. The maximum amount of tritium which distributed in crystal lattice of stainless steel is limitted by its solubility at room temperature. The other form of tritium in stainless steel is gaseous tritium that are trapped by defects, impurities, fractures, etc. within it. The gaseous tritium is several times more than the solid-dissolved tritium. (authors)

  13. Tritium production and processing in a Tokamak reactor

    International Nuclear Information System (INIS)

    Leger, D.

    1986-09-01

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

  14. 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

  15. Analysis of the organically bound tritium

    International Nuclear Information System (INIS)

    Baglan, N.; Alanic, G.

    2011-01-01

    In environmental samples, tritium is very often combined with the fraction of bulk water accumulated in the sample but also in the form of organically bound tritium. When the tritium is organically bound, 2 forms can coexist: the exchangeable fraction and the non-exchangeable fraction. The analysis of the different forms of tritium present in the sample is necessary to assess the sanitary hazards due to tritium. The total tritium is obtained from the analysis of the water released when the fresh sample is burnt while the organically bound tritium is obtained from the analysis of the water released when the dry extract of the sample is burnt. The measurement of the exchangeable fraction and the non-exchangeable fraction requires an additional stage of labile exchange. The exchangeable fraction is determined from the analysis of the water released during the labile exchange and the non-exchangeable fraction is determined from the water released during the combustion of the dry extract of the labile exchange

  16. Little tritium goes a long way

    International Nuclear Information System (INIS)

    Albright, D.; Taylor, T.B.

    1988-01-01

    Faced with mounting safety problems in its military production reactors, the Energy Department will soon ask Congress to fund the construction of at least one new multibillion dollar tritium production reactor. Energy estimates that building such a reactor could take ten years, and it says that in the interim it needs to continue producing tritium at the Savannah River reactors. In fact, it plans to resume operating its Savannah River reactors at full power as soon as possible. The United States must keep producing tritium if the US-Soviet nuclear arms race continues its present course. If the arms race continues, the Energy Department has two basic options: it could run the Savannah River reactors for several more decades or it could use these reactors until it has built a new one. Operating the Savannah River reactors at full or low power may be risky, even if they undergo extensive safety modifications, since no one knows at what power these reactors can be operated safely. Despite these pressing issues, most of the substantive debate about the role of tritium in nuclear weapons and the requirement for more tritium production is taking place in secret. The public debate largely ignores the broader questions of whether the United States needs to produce tritium and what impact possible agreements reducing nuclear arsenals might have on US tritium requirements

  17. Tritium Room Air Monitor Operating Experience Review

    Energy Technology Data Exchange (ETDEWEB)

    L. C. Cadwallader; B. J. Denny

    2008-09-01

    Monitoring the breathing air in tritium facility rooms for airborne tritium is a radiological safety requirement and a best practice for personnel safety. Besides audible alarms for room evacuation, these monitors often send signals for process shutdown, ventilation isolation, and cleanup system actuation to mitigate releases and prevent tritium spread to the environment. Therefore, these monitors are important not only to personnel safety but also to public safety and environmental protection. This paper presents an operating experience review of tritium monitor performance on demand during small (1 mCi to 1 Ci) operational releases, and intentional airborne inroom tritium release tests. The tritium tests provide monitor operation data to allow calculation of a statistical estimate for the reliability of monitors annunciating in actual tritium gas airborne release situations. The data show a failure to operate rate of 3.5E-06/monitor-hr with an upper bound of 4.7E-06, a failure to alarm on demand rate of 1.4E-02/demand with an upper bound of 4.4E-02, and a spurious alarm rate of 0.1 to 0.2/monitor-yr.

  18. Quick management of accidental tritium exposure cases

    International Nuclear Information System (INIS)

    Singh, V. P.; Badiger, N. M.; Managanvi, S. S.; Bhat, H. R.

    2008-01-01

    Removal half-life (RHL) of tritium is one of the best means for optimising medical treatment, reduction of committed effective dose (CED) and quick/easy handling of a large group of workers for medical treatment reference. The removal of tritium from the body depends on age, temperature, relative humidity and daily rainfall; so tritium removal rate, its follow-up and proper data analysis and recording are the best techniques for management of accidental acute tritium exposed cases. The decision of referring for medical treatment or medical intervention (MI) would be based on workers' tritium RHL history taken from their bodies at the facilities. The workers with tritium intake up to 1 ALI shall not be considered for medical treatment as it is a derived limit of annual total effective dose. The short-term MI may be considered for tritium intake of 1-10 ALI; however, if the results show intake ≥100 ALI, extended strong medical/therapeutic intervention may be recommended based on the severity of exposure for maximum CED reduction requirements and annual total effective dose limit. The methodology is very useful for pressurized heavy water reactors (PHWRs) which are mainly operated by Canada and India and future fusion reactor technologies. Proper management will optimise the cases for medical treatment and enhance public acceptance of nuclear fission and fusion reactor technologies. (authors)

  19. Quick management of accidental tritium exposure cases.

    Science.gov (United States)

    Singh, Vishwanath P; Badiger, N M; Managanvi, S S; Bhat, H R

    2012-07-01

    Removal half-life (RHL) of tritium is one of the best means for optimising medical treatment, reduction of committed effective dose (CED) and quick/easy handling of a large group of workers for medical treatment reference. The removal of tritium from the body depends on age, temperature, relative humidity and daily rainfall; so tritium removal rate, its follow-up and proper data analysis and recording are the best techniques for management of accidental acute tritium exposed cases. The decision of referring for medical treatment or medical intervention (MI) would be based on workers' tritium RHL history taken from their bodies at the facilities. The workers with tritium intake up to 1 ALI shall not be considered for medical treatment as it is a derived limit of annual total effective dose. The short-term MI may be considered for tritium intake of 1-10 ALI; however, if the results show intake ≥100 ALI, extended strong medical/therapeutic intervention may be recommended based on the severity of exposure for maximum CED reduction requirements and annual total effective dose limit. The methodology is very useful for pressurized heavy water reactors (PHWRs) which are mainly operated by Canada and India and future fusion reactor technologies. Proper management will optimise the cases for medical treatment and enhance public acceptance of nuclear fission and fusion reactor technologies.

  20. Isotopic fractionation of tritium in biological systems.

    Science.gov (United States)

    Le Goff, Pierre; Fromm, Michel; Vichot, Laurent; Badot, Pierre-Marie; Guétat, Philippe

    2014-04-01

    Isotopic fractionation of tritium is a highly relevant issue in radiation protection and requires certain radioecological considerations. Sound evaluation of this factor is indeed necessary to determine whether environmental compartments are enriched/depleted in tritium or if tritium is, on the contrary, isotopically well-distributed in a given system. The ubiquity of tritium and the standard analytical methods used to assay it may induce biases in both the measurement and the signification that is accorded to the so-called fractionation: based on an exhaustive review of the literature, we show how, sometimes large deviations may appear. It is shown that when comparing the non-exchangeable fraction of organically bound tritium (neOBT) to another fraction of tritium (e.g. tritiated water) the preparation of samples and the measurement of neOBT reported frequently led to underestimation of the ratio of tritium to hydrogen (T/H) in the non-exchangeable compartment by a factor of 5% to 50%. In the present study, corrections are proposed for most of the biological matrices studied so far. Nevertheless, the values of isotopic fractionation reported in the literature remain difficult to compare with each other, especially since the physical quantities and units often vary between authors. Some improvements are proposed to better define what should encompass the concepts of exchangeable and non-exchangeable fractions. Copyright © 2014 Elsevier Ltd. All rights reserved.

  1. Risks of tritium and their mitigation

    International Nuclear Information System (INIS)

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

    1992-01-01

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

  2. Measurement of tritium in environment, (2)

    International Nuclear Information System (INIS)

    Chaya, Ikuo; Kagami, Tadaaki; Hamamura, Norikatsu

    1975-01-01

    In order to know the amount of natural tritium in environmental water and also to know the tendency of tritium concentration in surface water which is necessary for the measurement of ground water age, the tritium concentration in rain, river, and sea water in Aichi Prefecture were measured. In order to make the appropriate utilization of ground water such as city water and hot springs and to elucidate the effect of ground water utilization on ground subsidence, it is desirable to clarify the state of underground water-bearing strata, the flow direction and flow speed of ground water, and the change of ground water quality owing to the flow. As the means of knowing the flow speed of ground water, the age determination with tritium was carried out. The amount of tritium was determined by measuring the concentrated samples with a liquid scintillation counter. The tritium concentration in river was 1.7 times as much as that in rain water, and it is attributed to the time difference from raining to flowing in rivers. The tritium concentration in sea water was high at the estuary of Kiso River, and about a half of it in the other places. The water of the hot spring source in Nobi Plain is the old ground water soaked more than 20 years ago. The city water sources utilizing ground water shallower than 300 m use both new and old ground water. (Kako, I.)

  3. The Safety and Tritium Applied Research (STAR) Facility: Status-2004

    International Nuclear Information System (INIS)

    Anderl, R.A.; Longhurst, G.R.; Pawelko, R.J.; Sharpe, J.P.; Schuetz, S.T.; Petti, D.A.

    2005-01-01

    The Safety and Tritium Applied Research (STAR) Facility, a US DOE National User Facility at the Idaho National Engineering and Environmental Laboratory (INEEL), comprises capabilities and infrastructure to support both tritium and non-tritium research activities important to the development of safe and environmentally friendly fusion energy. Research thrusts include (1) interactions of tritium and deuterium with plasma-facing-component (PFC) materials, (2) fusion safety issues [PFC material chemical reactivity and dust/debris generation, activation product mobilization, tritium behavior in fusion systems], and (3) molten salts and fusion liquids for tritium breeder and coolant applications. This paper updates the status of STAR and the capabilities for ongoing research activities, with an emphasis on the development, testing and integration of the infrastructure to support tritium research activities. Key elements of this infrastructure include a tritium storage and assay system, a tritium cleanup system to process glovebox and experiment tritiated effluent gases, and facility tritium monitoring systems

  4. Conceptual design of tritium accountancy system for LLCB TBM

    International Nuclear Information System (INIS)

    Patel, Rudreksh; Sircar, Amit

    2017-01-01

    Lead Lithium Ceramic Breeder (LLCB) Test Blanket Module (TBM) will be tested in ITER for performance evaluation of high grade of heat extraction and tritium breeding. The bred tritium in the breeder materials is extracted and recovered by Tritium Extraction System (TES), whereas tritium permeated from breeder materials to helium coolants, viz., primary coolant and secondary coolant, is recovered by Coolant Purification System (CPS). This recovered tritium has to be accounted before transferring it to tritium plant (i.e., ITER inner fuel). This tritium accountancy is performed by Tritium Accountancy System (TAS). In addition to tritium accountancy, TAS also provides necessary data for the validation of design and modelling tools.In this work, we have presented conceptual design of TAS. It also describes operational philosophy, process parameters, process flow diagram, and interface details with ITER tritium plant. (author)

  5. Tritium system design studies of fusion experimental breeder

    International Nuclear Information System (INIS)

    Deng Baiquan; Huang Jinhua

    2003-01-01

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

  6. Tritium

    Science.gov (United States)

    2011-11-01

    Fraction The probability that a triton injected into a reactor is burned in the reaction (1) before it escapes the confinement region in the case of MFE , or...vσ〉 = 3.68× 10−18 T 2/3 i exp ( − 19.94 T 1/3 i ) . (12) For a representative MFE ion temperature Ti = 20 keV, (13) we find from (12) that 〈vσ〉 = 3.22

  7. Tritium extraction technologies and DEMO requirements

    Energy Technology Data Exchange (ETDEWEB)

    Demange, D., E-mail: david.demange@kit.edu [Karlsruhe Institute of Technology, Institute for Technical Physics, Tritium Laboratory Karlsruhe, Hermann-von-Helmholtz-Platz 1, 76344 Eggenstein-Leopoldshafen (Germany); Antunes, R.; Borisevich, O.; Frances, L. [Karlsruhe Institute of Technology, Institute for Technical Physics, Tritium Laboratory Karlsruhe, Hermann-von-Helmholtz-Platz 1, 76344 Eggenstein-Leopoldshafen (Germany); Rapisarda, D. [Laboratorio Nacional de Fusión, EURATOM-CIEMAT, 28040 Madrid (Spain); Santucci, A. [ENEA for EUROfusion, Via E. Fermi 45, 00044 Frascati, Roma (Italy); Utili, M. [ENEA CR Brasimone, 40032 Camugnano, BO (Italy)

    2016-11-01

    Highlights: • We detail the R&D plan for tritium technology of the European DEMO breeding blanket. • We study advanced and efficient extraction techniques to improve tritium management. • We consider inorganic membranes and catalytic membrane reactor for solid blankets. • We consider permeator against vacuum and vacuum sieve tray for liquid blankets. - Abstract: The conceptual design of the tritium extraction system (TES) for the European DEMO reactor is worked out in parallel for four different breeding blankets (BB) retained by EUROfusion. The TES design has to be tackled in an integrated manner optimizing the synergy with the directly interfacing inner fuel cycle, while minimizing the tritium permeation into the coolant. Considering DEMO requirements, it is most likely that only advanced technologies will be suitable for the tritium extraction systems of the BB. This paper overviews the European work programme for R&D on tritium technology for the DEMO BB, summaries the general first outcomes, and details the specific and comprehensive R&D program to study experimentally immature but promising technologies such as vacuum sieve tray or permeator against vacuum for tritium extraction from PbLi, and advanced inorganic membranes and catalytic membrane reactor for tritium extraction from He. These techniques are simple, fully continuous, likely compact with contained energy consumption. Several European Laboratories are joining their efforts to deploy several new experimental setups to accommodate the tests campaigns that will cover small scale experiments with tritium and inactive medium scale tests so as to improve the technology readiness level of these advanced processes.

  8. 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

  9. 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

  10. Tritium kinetics in a freshwater marsh ecosystem

    International Nuclear Information System (INIS)

    Adams, L.W.

    1976-01-01

    Ten curies of tritium (as tritiated water, HTO) were applied to a 2-ha enclosed Lake Erie marsh in northwestern Ohio on 29 October 1973. Tritium kinetics in the marsh water, bottom sediment, and selected aquatic plants and animals were determined. Following HTO application, peak tritium levels in the sediment were observed on day 13 in the top 1-cm layer, on day 27 at the 5-cm depth, and on day 64 at the 10-cm depth. Peak levels at 15 and 20 cm were not discernible, although there was some movement of HTO to the 20-cm depth. A model based on diffusion theory described tritium movement through the sediment. Unbound and bound tritium levels in curly-leaf pondweed (Potamogeton crispus), pickerelweed (Pontederia cordata), and smartweed (Polygonum lapathifolium) generally tended to follow tritium levels in marsh water. The unbound tritium:marsh water tritium ratio was significantly larger (P < 0.001) in curly-leaf pondweed than in either of the two emergents. Tritium uptake into the unbound compartments of crayfish (Procambarus blandingi), carp (Cyprinus carpio), and bluegills (Lepomis macrochirus) was rapid. For crayfish, maximum HTO levels were observed on days 3 and 2 for viscera and muscle, respectively. Unbound HTO in carp viscera peaked on day 2, and levels in carp muscle reached a maximum in 4 hours. Maximum levels of unbound HTO in bluegill viscera and muscle were observed on day 1. After peak levels were obtained, unbound HTO paralleled marsh water HTO activity in all species. Tritium uptake into the bound compartments was not as rapid nor were the levels as high as for unbound HTO in any of the species. Peak bound levels in crayfish viscera were observed on day 20 and maximum levels in muscle were noted on day 10. Bound tritium in carp viscera and muscle reached maximum levels on day 20. In bluegills, peaks were reached on days 7 and 5 for viscera and muscle, respectively. Bound tritium in all species decreased following maximum levels

  11. Review of general tritium accountancy techniques

    International Nuclear Information System (INIS)

    Vassallo, G.; Engelmann, U.

    1995-01-01

    The accountancy of material in any facility forms an integral part of good housekeeping practices. However, for materials such as tritium, a combination of safety, security and economic reasons often demands that a comprehensive material control program be implemented. Within a tritium facility, the isotope is usually stored at a central magazine from where it can be distributed to and collected from process plant and experiments and received from external suppliers. This paper outlines the routine magazine measurement techniques employed for quantitatively assaying tritium for such control purposes and reviews the advantages and drawbacks of various methods. 10 refs., 2 figs., 2 tabs

  12. Preparation of honey sample for tritium monitoring

    International Nuclear Information System (INIS)

    Chen Bingru; Wang Chenlian; Wang Weihua

    1989-01-01

    The method of preparation of honey sample for tritium monitoring was described. The equipments consist of an air and honey supply system, a quartz combustor with CM-type monolithic combustion catalyst and a condensation system. In the equipments, honey sample was converted into cooling water by the distilling, cracking and carbonizing procedures for tritium counting. The recovery ratio is 99.0 ± 4.5 percent for tritiated water and 96.0 ± 2.0 for tritiated organic compounds. It is a feasible preparing method for the total tritium monitoring in honey sample

  13. Conversion of tritium gas to tritiated water

    International Nuclear Information System (INIS)

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

    1979-05-01

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

  14. Electrolytic gettering of tritium from air

    International Nuclear Information System (INIS)

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

    1983-01-01

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

  15. The tritium and the controlled fusion reactors

    International Nuclear Information System (INIS)

    Leger, D.; Rouyer, J.L.

    1986-04-01

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

  16. Management of Tritium in European Spallation Source

    DEFF Research Database (Denmark)

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

    2015-01-01

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

  17. 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

  18. 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.)

  19. 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.

  20. 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.

  1. Tritium inventory measurements using calorimetry

    International Nuclear Information System (INIS)

    Kapulla, H.; Kraemer, R.; Heine, R.

    1992-01-01

    In the past calorimetry has been developed as a powerful tool in radiometrology. Calorimetric methods have been applied for the determination of activities, half lives and mean energies released during the disintegration of radioactive isotopes. The fundamental factors and relations which determine the power output of radioactive samples are presented and some basic calorimeter principles are discussed in this paper. At the Kernforschungszentrum Karlsruhe (KfK) a family of 3 calorimeters has been developed to measure the energy release from radiative waste products arising from reprocessing operations. With these calorimeters, radiative samples with sizes from a few cm 3 to 2 ·10 5 cm 3 and heat ratings ranging from a few nW to kW can be measured. After modifications of tits inner part the most sensitive calorimeter among the three calorimeters mentioned above would be best suited for measuring the tritium inventory in T-getters of the Amersham-type

  2. Environmental monitoring of molecular tritium

    Energy Technology Data Exchange (ETDEWEB)

    Ichimasa, M.; Ichimasa, Y.; Akita, Y. (Ibaraki Univ., Mito (Japan). Faculty of Science); Suzuki, M.; Obayashi, H.; Sakuma, Y.

    1992-01-01

    The oxidation of atmospheric molecular tritium (HT) in vegetation was determined by in vitro experiments for various kinds of woody and herbaceous plant leaves, mosses and lichens taken from a forest and a garden in Ibaraki prefecture and a forest in Gifu prefecture, and comparison of the HT oxidation activity in vegetation was made with those in its neighboring surface soil (0-5cm in depth). The oxidation of HT in woody plant leaves was extremely low, only about 1/10000-1/1000 that in the surface soil as well as herbaceous plant leaves with some exception, whereas HT oxidation in mosses and lichens was 50-500 times that in pine needles. These results suggest the usefulness of mosses and lichens as monitor vegetation for accidental release of HT into the environment. (author).

  3. 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)

  4. Tritium experiments on components for fusion fuel processing at the Tritium Systems Test Assembly

    International Nuclear Information System (INIS)

    Konishi, S.; Yoshida, H.; Naruse, Y.; Carlson, R.V.; Binning, K.E.; Bartlit, J.R.; Anderson, J.L.

    1990-01-01

    Under a collaborative agreement between US and Japan, two tritium processing components, a palladium diffuser and a ceramic electrolysis cell have been tested with tritium for application to a Fuel Cleanup System (FCU) for plasma exhaust processing at the Los Alamos National Laboratory. The fundamental characteristics, compatibility with tritium, impurities effects with tritium, and long-term behavior of the components, were studied over a three year period. Based on these studies, an integrated process loop, ''JAERI Fuel Cleanup System'' equipped with above components was installed at the TSTA for full scale demonstration of the plasma exhaust reprocessing

  5. 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.

  6. Review of tritium behavior in HTGR systems

    International Nuclear Information System (INIS)

    Gainey, B.W.

    1976-01-01

    The available experimental evidence from laboratory and reactor studies pertaining to tritium production, capture, release, and transport within an HTGR leading to release to the environment is reviewed. Possible mechanisms for release, capture, and transport are considered and a simple model was used to calculate the expected tritium release from HTGRs. Comparison with Federal regulations governing tritium release confirm that expected HTGR releases will be well within the allowable release limits. Releases from HTGRs are expected to be somewhat less than from LWRs based on the published LWR operating data. Areas of research deserving further study are defined but it is concluded that a tritium surveillance at Fort St. Vrain is the most immediate need

  7. Tritium-management survey of Wolsong 1

    International Nuclear Information System (INIS)

    Allsop, P.J.; Boss, C.R.; Song, M-J.; Son, S-H.; Choi, J-K.

    1996-10-01

    Commissioned in 1983, Wolsong 1 has had one of the best lifetime capacity factors in the world. It has also maintained tritium emissions and heavy-water losses at or below those of similar CANDU 6 reactors. To further ensure that emissions remain as low as reasonably achievable (ALARA), Wolsong 1, AECL and the KEPC0 (Korean Electric Power Company)Research Center collaborated on a survey of tritium management at Wolsong 1 during the spring of 1995. This survey identified similarities and differences between Wolsong 1 and the Canadian CANDU 6 stations. It also corroborated several of Wolsong 1's plans to further refine and upgrade tritium management. This report summarizes those aspects of the Wolsong 1 tritium survey. (author)

  8. Tritium Measurements in Slovenia - Chronology Till 2004

    International Nuclear Information System (INIS)

    Logar, Jasmina Kozar; Vaupotic, Janja; Kobal, Ivan

    2005-01-01

    Almost all the analyses of tritium in Slovenia have been performed by the tritium laboratory at the Jozef Stefan Institute. Nearly 90 % of its measurements have been covered by two national programs, both approved by the Slovenian Nuclear Safety Administration: the radioactive monitoring program in the environs of Krsko Nuclear Power Plant (KNPP) and the program of global radioactive contamination monitoring in the environment. These programs include samples of groundwaters, surface waters, precipitation and drinking waters, as well as liquid and gaseous effluents from KNPP. Tritium was determined in some research projects and in hydrological studies of thermal waters, groundwater and coalmine waters. Tritium in the Karst region was mapped as well as the springs of entire territory of Slovenia. Around 5500 samples have been analyzed up to 2004

  9. 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

  10. Survey of pumps for tritium gas

    International Nuclear Information System (INIS)

    Dowell, T.M.

    1983-05-01

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

  11. 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

  12. Tritium detection in installations and in environment

    International Nuclear Information System (INIS)

    Calando, J.P.

    1986-04-01

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

  13. Tritium Inventory in ARIES-AT

    International Nuclear Information System (INIS)

    Longhurst, Glen R.

    2001-01-01

    This report documents an investigation into the tritium inventory expected in the ARIES-AT fusion reactor. ARIES-AT features silicon carbide fibers in a silicon carbide matrix as its primary construction. It uses the same fusion power core as the previous ARIES-RS. Based on experimental results of several researchers, consideration was given to swelling, sputtering, film coatings, erosion, and implantation. Estimates were made of tritium inventory using the TMAP4 code. About 700 g of tritium may be expected in the machine, two thirds of which would reside in the first wall. Under assumed accident conditions that involve first wall temperatures up to 1000 C, evolution of retained tritium may be expected to vary from 0.8 to nearly 40 percent depending on the temperature of the first wall

  14. Methods of tritium recovery from molten lithium

    International Nuclear Information System (INIS)

    Farookhi, R.; Rogers, J.E.

    1968-01-01

    It is important to keep the tritium inventory in a blanket of a thermonuclear reactor at a low level both to eliminate possible hydriding of structural components and to reduce inventory cost. Removing the tritium from a lithium blanket by fractional distillation, flash vaporization, and fractional crystallization was investigated. No definitive data are available either on the vapor-liquid equilibrium between lithium and tritium at low T 2 concentrations, or on the rate of formation and decomposition of lithium tritide. The final distinction between the recovery systems discussed in this report will depend on such data, but presently distillation appears to be the best alternate to the diffusion scheme proposed by A.P. Fraas. The capital cost of equipment necessary to remove tritium by distillation appears to be greater than 10 million dollars for a 5000 MW system, whereas the capital cost associated with the diffusion process has been estimated to be 4 million dollars

  15. Investigation of tritium in the aquatic environment

    International Nuclear Information System (INIS)

    Cohen, L.K.

    1977-01-01

    The behavior, cycling and distribution of tritium in an aquatic ecosystem was studied in the field and in the laboratory from 1969 through 1971. Field studies were conducted in the Hudson River Estuary, encompassing a 30 mile region centered about the Indian Point Nuclear Plant. Samples of water, bottom sediment, rooted emergent aquatic plants, fish, and precipitation were collected over a year and a half period from more than 15 locations. Specialized equipment and systems were built to combust and freeze-dry aquatic media to remove and recover the loose water and convert the bound tritium into an aqueous form. An electrolysis system was set up to enrich the tritium concentrations in the aqueous samples to improve the analytical sensitivity. Liquid scintillation techniques were refined to measure the tritium activity in the samples. Over 300 samples were analyzed during the course of the study

  16. Leaching of tritium from a cement composite

    International Nuclear Information System (INIS)

    Matsuzuru, Hideo; Ito, Akihiko

    1978-10-01

    Leaching of tritium from cement composites into an aqueous phase has been studied to evaluate the safety of incorporation of the tritiated liquid waste into cement. Leaching tests were performed by the method recommended by the International Atomic Energy Agency. The Leaching fraction was measured as functions of waste-cement ratio (Wa/C), temperature of leachant and curing time. The tritium leachability of cement in the long term test follows the order: alumina cement portland cement slag cement. The fraction of tritium leached increases with increasing Wa/C and temperature and decreasing curing period. A deionized water as a leachant gives a slightly higher leachability than synthetic sea water. The amount leached of tritium from a 200 l drum size specimen was estimated on the basis of the above results. (author)

  17. 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.

  18. Tritium means of detection and of protection

    International Nuclear Information System (INIS)

    Sutra-Fourcade, Y.

    1967-01-01

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

  19. Tritium handling facility at KMS Fusion Inc

    International Nuclear Information System (INIS)

    Bowman, C.C.; Vis, V.A.

    1990-01-01

    The tritium facility at KMS Fusion, Inc. supports the inertial confinement fusion research program. The main function of the facility is to fill glass and polymer Microshell (TM) capsules (small fuel containers) to a maximum pressure of 100 atm with tritium (T 2 ) or deuterium--tritium (DT). The recent upgrade of the facility allows us to fill Microshell capsules to a maximum pressure of 200 atm. A second fill port allows us to run long term fills of Macroshell (TM) capsules (large fuel containers) concurrently. The principle processes of the system are: (1) storage of the tritium as a uranium hydride; (2) pressure intensification using cryogenics; and (3) filling of the shells by permeation at elevated temperatures. The design of the facility was centered around a NRC license limit of 6000 Ci

  20. Tritium Issues in Next Step Devices

    International Nuclear Information System (INIS)

    C.H. Skinner; G. Federici

    2001-01-01

    Tritium issues will play a central role in the performance and operation of next-step deuterium-tritium (DT) burning plasma tokamaks and the safety aspects associated with tritium will attract intense public scrutiny. The orders-of-magnitude increase in duty cycle and stored energy will be a much larger change than the increase in plasma performance necessary to achieve high fusion gain and ignition. Erosion of plasma-facing components will scale up with the pulse length from being barely measurable on existing machines to centimeter scale. Magnetic Fusion Energy (MFE) devices with carbon plasma-facing components will accumulate tritium by co-deposition with the eroded carbon and this will strongly constrain plasma operations. We report on a novel laser-based method to remove co-deposited tritium from carbon plasma-facing components in tokamaks. A major fraction of the tritium trapped in a co-deposited layer during the deuterium-tritium (DT) campaign on the Tokamak Fusion Test Reactor (TFTR) was released by heating with a scanning laser beam. This technique offers the potential for tritium removal in a next-step DT device without the use of oxidation and the associated deconditioning of the plasma-facing surfaces and expense of processing large quantities of tritium oxide. The operational lifetime of alternative materials such as tungsten has significant uncertainties due to melt layer loss during disruptions. Production of dust and flakes will need careful monitoring and minimization, and control and accountancy of the tritium inventory will be critical issues. Many of the tritium issues in Inertial Fusion Energy (IFE) are similar to MFE, but some, for example those associated with the target factory, are unique to IFE. The plasma-edge region in a tokamak has greater complexity than the core due to lack of poloidal symmetry and nonlinear feedback between the plasma and wall. Sparse diagnostic coverage and low dedicated experimental run time has hampered the