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)

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 A cascaded system is established, in which effluent streams enriched and depleted in tritium can be withdrawn.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

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

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...

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.)

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.)

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

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

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

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

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...

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.)

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)

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

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

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.

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.)

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.)

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

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)

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)

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)

10 CFR 150.19 - Submission to Commission of tritium reports.

Science.gov (United States)

2010-01-01

... 10 Energy 2 2010-01-01 2010-01-01 false Submission to Commission of tritium reports. 150.19... Agreement States § 150.19 Submission to Commission of tritium reports. (a)-(b) [Reserved] (c) Except as... authorized to possess tritium shall report promptly to the appropriate NRC Regional Office as shown in...

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

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)

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)

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

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.)

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.

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

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

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)

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

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)

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)

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

Determinations of tritium levels in urine and blood samples, medical checkups of persons employed at RC Seibersdorf

International Nuclear Information System (INIS)

Irlweck, K.; Teherani, D.K.

1975-07-01

Tritium determinations in urine and blood samples were performed with a liquid scintillation counter (Tri Carb No. 3375, PACKARD). In urine samples tritiated water (HTO) was measured after separation of organic substances by adsorption with activated charcoal and following distillation to dryness. In some urine and blood samples total Tritium content was determinated by conbustion in a sample Oxidizer (Mod. 306, PACKARD). Detection limits for HTO and total Tritium measurements were 2,5 pCi/ml and 7 or 15 pCi/ml respectively, taking 2 sigma of statistical error of background values. Tritiumconcentrations in daily urine of occupational exposed persons, employed in RC Seibersdorf occurred up to 8 pCi HTO/ml. An arithmetic mean was 3,85+-2,11 pCi/ml from investigations on 16 persons. Tritiumcontent in urine samples of occupational non exposed persons were about the same level up to 10 pCi HTO/ml. An arithmetic mean was 3,70+-2,65 pCi/ml from measurements on 20 persons. Statistical error of single values was sigma=+-1,85 pCi/ml. There was found no significantly higher concentration in urine of occupational exposed persons compared with a group of non exposed ones. Total Tritium content in urine samples seemed to be somewhat higher than HTO concentrations, also for occupational non exposed persons. Tritium levels in blood were notably higher than have to be expected assuming homogeneous distribution of HTO in body fluids. For occupational exposed persons in RC Seibersdorf Tritium concentrations between 26-58 pCi/ml were found. An estimation about Tritium intake based on such results showed no more than 0,5% of maximum permissible intake for occupational exposed persons in the most unfavorable case. For occupational non exposed persons total Tritium levels in blood were only about 10,7+-5,8 pCi/ml (arithmetic mean of measurements on 15 persons). (author)

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

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)

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)

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

Development of a tritium recovery system from CANDU tritium removal facility

International Nuclear Information System (INIS)

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

2015-01-01

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

Development of a tritium recovery system from CANDU tritium removal facility

Energy Technology Data Exchange (ETDEWEB)

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

2015-03-15

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

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%

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.

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.

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.)

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

10 CFR 30.19 - Self-luminous products containing tritium, krypton-85, or promethium-147.

Science.gov (United States)

2010-01-01

... 10 Energy 1 2010-01-01 2010-01-01 false Self-luminous products containing tritium, krypton-85, or..., krypton-85, or promethium-147. (a) Except for persons who manufacture, process, produce, or initially transfer for sale or distribution self-luminous products containing tritium, krypton-85, or promethium-147...

10 CFR 32.22 - Self-luminous products containing tritium, krypton-85 or promethium-147: Requirements for license...

Science.gov (United States)

2010-01-01

... 10 Energy 1 2010-01-01 2010-01-01 false Self-luminous products containing tritium, krypton-85 or... containing tritium, krypton-85 or promethium-147: Requirements for license to manufacture, process, produce... self-luminous products containing tritium, krypton-85, or promethium-147, or to initially transfer such...

Conception and operation of a 10 kCi liquid tritium target for the study of tritium nucleus by electron diffusion: 3H(e,e)

International Nuclear Information System (INIS)

Juster, F.P.

1986-06-01

We describe the conception and operation of an experimental setup, specially suited for the study of the nuclear structure of tritium by elastic electron scattering at intermediate energy. The experiment has been conducted at the ALS 700 MeV electron linac (Saclay, France). The radioactive nature of tritium has led to the design of a new target, suited for handling reliably ten kilocuries of tritium (one gram). The tritium is contained in three sealed envelopes. Initially a high pressure gas (23 bars) at room temperature, the tritium is cooled down to liquefaction by thermal conduction through a solid, without breaking any seal. The beam path and the scattered trajectories cross thin metallic windows. Additional protection, during the presence of personnel, is provided by a heavy container, remotely operated. Any leak in the containement vessels is detected by changes in pressure and/or temperature gauges, monitored by two independent processors. These processors handle the operation of the outer container, the beam switching and the spare venting system. No tritium leak has been detected during a total six-week run. The tritium liquefies in a cylindrical target, 5 cm long and 1 cm in diameter. A beam of 10 microamperes, in the 200-700 MeV, has been measured. The charge and magnetic form factors of tritium have been measured up to a momentum transfer of 31.3 fm -2 [fr

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

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)

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)

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

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

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

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

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

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

International Nuclear Information System (INIS)

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

1986-01-01

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

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)

The Chalk River Tritium Extraction Plant

International Nuclear Information System (INIS)

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

1990-01-01

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

The Chalk River Tritium Extraction Plant

Energy Technology Data Exchange (ETDEWEB)

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

1990-07-01

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

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.)

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.)

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.)

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

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

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

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%

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

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

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.)

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

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)

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

International Nuclear Information System (INIS)

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

1984-01-01

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

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

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.).

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.

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

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

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

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

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

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

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

Tritium concentrations in natural waters in Japan before use of a large quantity of tritium on its fusion program

International Nuclear Information System (INIS)

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

1989-01-01

To clarify environmental tritium levels in Japan before use of a large quantity of tritium on its fusion program, the authors analyzed the tritium concentrations in various water samples, such as rain, river, lake, coastal sea and deep sea waters in Japan. The tritium concentrations in rain water were high at higher latitude. The definite differences of the tritium concentrations due to the weather conditions or seasons were not observed. The average tritium concentration in river water was 51.5 pCi/l in 1982 and that in lake water was 63.5 pCi/l in 1983. The vertical profiles of the tritium concentrations in the representative lakes were almost homogeneous except surface water. The average tritium concentrations in coastal seawater were about 20 pCi/l in both 1982 and 1983. The tendency of the increased tritium level with latitude as reported in literature was not observed by these experiments. Tritium levels in natural water in small isolated islands were lower than those at other places. In the Japan Sea, it was recognized that tritium was distributed down to around 2000 m in depth. This means that the more active vertical mixing of water masses than that in the Pacific Ocean is taking place. (author)

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

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)

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

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

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

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.

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

Energy Technology Data Exchange (ETDEWEB)

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

2017-04-01

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

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

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.

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.

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

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

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

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

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

Energy Technology Data Exchange (ETDEWEB)

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

2016-06-15

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

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

International Nuclear Information System (INIS)

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

1985-04-01

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

Tritium 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

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

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

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.

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)

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

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

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

Tritium recapture behavior at a nuclear power reactor due to airborne releases.

Science.gov (United States)

Harris, Jason T; Miller, David W; Foster, Doug W

2008-08-01

This paper describes the initiatives taken by Cook Nuclear Plant to study the on-site behavior of recaptured tritium released in its airborne effluents. Recapture is the process where a released radioactive effluent, in this case tritium, is brought back on-site through some mechanism. Precipitation, shifts in wind direction, or anthropogenic structures that restrict or alter effluent movement can all lead to recapture. The investigation was started after tritium was detected in the north storm drain outfall. Recent inadvertent tritium releases by several other nuclear power plants, many of which entered the groundwater, have led to increased surveillance and scrutiny by regulatory authorities and the general public. To determine the source of tritium in the outfall, an on-site surface water, well water, rainwater and air-conditioning condensate monitoring program was begun. Washout coefficients were also determined to compare with results reported by other nuclear power plants. Program monitoring revealed detectable tritium concentrations in several precipitation sample locations downwind of the two monitored containment building release vents. Tritium was found in higher concentrations in air-conditioning condensate, with a mean value of 528 Bq L(-1) (14,300 pCi L(-1)). The condensate, and to a lesser extent rainwater, were contributing to the tritium found in the north storm drain outfall. Maximum concentration values for each sample type were used to estimate the most conservative dose. A maximum dose of 1.1 x 10(-10) mSv (1.1 x 10(-8) mrem) total body was calculated to determine the health impact of the tritium detected.

Distribution of tritium in a nuclear process heat plant with HTR

International Nuclear Information System (INIS)

Steinwarz, W.; Stoever, D.; Hecker, R.; Thiele, W.

1984-01-01

The application of HTR-process heat in chemical processes involves low contamination of the product by tritium permeation through the heat exchanger walls. According to conservative assumptions for the tritium release rate and based on experimental permeation data of the German R und D-program a tritium concentration in the PNP-product gas of about 10 pCi/g was calculated. The domestic use of the product gas in unvented kitchen ranges as the most important direct radiation exposure pathway then leads to an effective equivalent radiation dose of only 20 μrem/a. (orig.)

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

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

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.

1991-07-01

Tritium-handling apparatus has been decontaminated as part of the shutdown of the LLNL Tritium Facility. Two stainless-steel gloveboxes that had been used to process lithium deuteride-tritide (LiDT) salt were decontaminated using the Portable Cleanup System so that they could be flushed with room air through the facility ventilation system. Further surface decontamination was performed by scrubbing the interior with paper towels and ethyl alcohol or Swish trademark. The surface contamination, as shown by swipe surveys, was reduced from 4x10 4 --10 6 disintegrations per minute (dpm)/cm 2 to 2x10 2 --4x10 4 dpm/cm 2 . 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

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

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)

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

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

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

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.)

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.)

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.

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)

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)

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.)

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)

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

International Nuclear Information System (INIS)

Hoek, J. van den

1982-01-01

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

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

Energy Technology Data Exchange (ETDEWEB)

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

1982-01-01

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

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

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.)

Tritium surveillance around nuclear facilities in Japan

International Nuclear Information System (INIS)

Inoue, Y.; Kasida, Y.

1978-01-01

In order to measure the tritium levels in the environmental water around the nuclear facilities, the tritium surveillance program began in 1967 locally at Tsuruga and Mihama districts. Nowadays it has been expanded to the ten commercial nuclear power stations and three nuclear facilities. For samples whose tritium concentration is believed less than about 100 pCi/l, they were electrolytically enriched, and then counted by the liquid scintillation counter. Some of samples believed higher than 100 pCi/l were analysed without any enrichment by the low background liquid scintillation counters, Aloka LB 600 or Aloka LB 1. The results of each station are listed in Table. The sampling points corresponding to each results are shown in Figure. Tritium from the effluent was not reflected in all the land water and the tap water around the nuclear power stations and the nuclear facilities. Tritium concentration in rivers, streams, and reservoirs (pools) decreased exponentially from about 600 pCi/l in 1967 to about 150 pCi/l in 1972 at Tsuruga and Mihama, and 360 pCi/l in 1968 to 120 pCi/l in 1973 at Genkai, with the half life of about 2.5 years in both cases. After around 1972, tritium levels of river system in all districts of Japan kept nearly constant up to the end of 1975 and they were in the range from 100 to 300 pCi/l corresponding to the districts. Thereafter, it seems to start to decrease again in 1976. Sea water sampled at the intake of the station or on the seashore far from the outlet was regarded not to be influenced by the effluent from the nuclear reactors or facilities. Tritium concentration in these coastal waters decreased from 100 - 300 pCi/l in 1971 to 30 - 40 pCi/l in 1972 in Fukushima, Ibaraki and Fukui prefectures. (author)

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

Tritium-caused background currents in electron multipliers

International Nuclear Information System (INIS)

Malinowski, M.E.

1979-05-01

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

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)

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)

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

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)

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.)

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

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.

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)

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

International Nuclear Information System (INIS)

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

1980-01-01

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

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

Effect of tritium (tritium water) on prenatal and postnatal development of rats

International Nuclear Information System (INIS)

Bajrakova, A.; Baev, I.; Yagova, A.

1983-01-01

Female rats were injected intraperitoneally on the first day after their fecundation with 3,7 kBq/g b.w. tritium water - activity which under these conditions does not increase prenatal death rate. The postnatal development of the born alive was traced in respect to the lethality rate and growth rate (mean bodily weight in dynamics up to the 60-th day p.p.) and compared with that of the offsprings from the control group. It was shown that the used activity tritium water during the initial stages of embryonic development does not result in deviations from the norm. (authors)

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

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.

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)

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

Energy Technology Data Exchange (ETDEWEB)

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

2014-07-01

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

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

Confinement and Tritium Stripping Systems for APT Tritium Processing

Energy Technology Data Exchange (ETDEWEB)

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

1997-10-20

This report identifies functions and requirements for the tritium process confinement and clean-up system (PCCS) and provides supporting technical information for the selection and design of tritium confinement, clean-up (stripping) and recovery technologies for new tritium processing facilities in the Accelerator for the Production of Tritium (APT). The results of a survey of tritium confinement and clean-up systems for large-scale tritium handling facilities and recommendations for the APT are also presented.

Confinement and Tritium Stripping Systems for APT Tritium Processing

International Nuclear Information System (INIS)

Hsu, R.H.; Heung, L.K.

1997-01-01

This report identifies functions and requirements for the tritium process confinement and clean-up system (PCCS) and provides supporting technical information for the selection and design of tritium confinement, clean-up (stripping) and recovery technologies for new tritium processing facilities in the Accelerator for the Production of Tritium (APT). The results of a survey of tritium confinement and clean-up systems for large-scale tritium handling facilities and recommendations for the APT are also presented

Tritium sorption in lithium-bismuth and lithium-aluminum alloys

International Nuclear Information System (INIS)

Talbot, J.B.; Smith, F.J.; Land, J.F.; Barton, P.

1976-01-01

The sorption of tritium by molten lithium-bismuth, Li-Bi (15 at.% lithium), and solid equiatomic lithium-aluminum, Li-Al, was investigated to evaluate the potential application of both materials in controlled thermonuclear reactors. The solubility of tritium in molten Li-Bi is less than 0.1 ppb at 500 - 700 0 C and tritium partial pressures of 10 -1 - 10 -3 Torr. Therefore, extraction of tritium from molten Li 2 BeF 4 salt with Li-Bi is not practical. The solubility of hydrogen in solid Li-Al (50 - 50 at.%) at 500 0 C follows Sieverts' Law; the Sieverts' constant was measured to be 1.9 (+-0.1) X 10 4 Torrsup(1/2)/atomic fraction. Tritium sorption in Li-Al ranged from 0.01 to 7 ppm at 400 - 600 0 C at respective tritium partial pressures of 0.14 - 0.52 Torr. (Auth.)

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)

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

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)

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

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.)

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

Tritium stripping in a nitrogen glovebox using SAES St 198

International Nuclear Information System (INIS)

Klein, J.E.; Wermer, J.R.

1994-01-01

SAES metal getter material St 198 was chosen for glovebox stripper tests to evaluate its effectiveness of removing tritium from a nitrogen atmosphere. The St 198 material is unique from a number of other metal hydride-based getter materials in that it is relatively inert to nitrogen and can thus be used in nitrogen glovebox atmospheres. Six tritium stripper experiments which mock-up the use of a SAES St 198 stripper bed for a full-scale (10,500 liter) nitrogen glovebox have been completed. Experiments consisted of a release of small quantity of protium/deuterium spiked with tritium which were scaled to simulate tritium releases of 0.1 g., 1.0 g., and 10 g. into the glovebox. The tritium spike allows detection using tritium ion chambers. The St 198 stripper system produced a reduction in tritium activity of approximately two orders of magnitude in 24 hours (6--8 atmosphere turn-overs) of stripper operation

Tritium transport calculations for the IFMIF Tritium Release Test Module

Energy Technology Data Exchange (ETDEWEB)

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

2014-10-15

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

Tritium transport calculations for the IFMIF Tritium Release Test Module

International Nuclear Information System (INIS)

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

2014-01-01

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

Tritium 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)

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

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.)

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

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.

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.)

Tritium waste control: April--September 1977

International Nuclear Information System (INIS)

1978-01-01

A pilot scale system was used in an initial experiment to investigate the combined-electrolysis-catalytic-exchange process (CECE) for the detritiation of water. Data taken during the experiment indicate the process does indeed strip tritium from gaseous hydrogen at the top and concentrate it in water at the bottom of the catalyst-filled column. A high activity tritiated water electrolysis system was designed and built using a solid polymer electrolyte (SPE) cell. The system was successfully operated at currents up to 50 A using deionized tap water. Triplicate samples of cement, cement-plaster (1:1 ratio by weight), and cement-plaster (1:1 ratio by volume) were injected with 386 Ci of tritium. Preliminary results indicate Type III Portland cement retains the tritium slightly better than the cement-plaster mixtures. The tritium release study of actual waste burial packages is continuing. The fractional release is 1 x 10 -5 on a 4-y old package, only 4 x 10 -7 on 3-y old packages, and 1 x 10 -9 on a 1-y old package. Pressure increase and gas composition determinations were repeated for octane (activity = 1000 Ci/liter) with and without tritium fixation using argon as the initial overgas. Pressure buildup measurements for octane without fixation were repeated a third time using hydrogen gas. The rate of pressure increase did not change significantly from previously determined values. Four elemental tritium samples were released into a laboratory to determine the efficiency of the Emergency Containment System. The ventilation system was modified during the fourth experiment to minimize leakage

Tritium extraction from neutron-irradiated lithium aluminate

International Nuclear Information System (INIS)

Garcia H, F.

1995-01-01

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

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)

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)

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

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

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

Tritium permeation and recovery for the Flibe/He blanket design

International Nuclear Information System (INIS)

Moir, R.

1984-10-01

This study assumes tritium to be a gas dissolved in molten salt, with TF formation suppressed. Tritium permeates readily through the hot steel tubes of the reactor and steam generator and will leak into the steam system at the rate of about one gram per day in the absence of special permeation barriers, assuming that 1% of the helium coolant flow rate is processed for tritium recovery at 90% efficiency per pass. Tritiated water in the steam system is a personnel hazard at concentration levels well below one part per million and this level would soon be reached without costly isotopic processing. Alternatively, including a combination of permeation barriers on reactor and steam generator tubes and molten salt processing is estimated to reduce the leak rate into the steam system by over two orders of magnitude. For the option with the lowest estimated leak rate, 55 Ci/d, it may be possible to purge the steam system continuously to prevent tritiated water buildup. At best, isotopic separation of dilute tritiated water may not be necessary and for higher leak-rate options the isotopic processing rate can be reduced. The proposed permeation barrier for the reactor tubes is a 10 μm layer of tungsten which, in principle, will reduce tritium blanket permeation by a factor of about 300 below the bare-steel rate

Secondary containment system for a high tritium research cryostat

International Nuclear Information System (INIS)

Tsugawa, R.T.; Fearon, D.; Souers, P.C.; Hickman, R.G.; Roberts, P.E.

1976-01-01

A 4.2- to 300-K liquid helium cryostat has been constructed for cryogenic samples of D--T containing up to 4 x 10 14 dis/s (10,000 Ci) of tritium radioactivity. The cryostat is enclosed in a secondary box, which acts as the ultimate container in case of a tritium release. Dry argon is flushed through the box, and the box atmosphere is monitored for tritium, oxygen, and water vapor. A rupture disk and abort tank protect the box atmosphere in case the sample cell breaks. If tritium breaks into the box, a powdered uranium getter trap reduces the 4 x 10 14 dis/s (10,000 Ci) to 4 x 10 9 dis/s (0.1 Ci) in 24 h. A backup palladium--zeolite getter system goes into operation if an overabundance of oxygen contaminates the uranium getter

Tritium management in fusion synfuel designs

International Nuclear Information System (INIS)

Galloway, T.R.

1980-01-01

Two blanket types are being studied: a lithium-sodium pool boiler and a lithium-oxide- or lithium-sodium pool boiler and a lithium-oxide- or aluminate-microsphere moving bed. For each, a wide variety of current technology was considered in handling the tritium. Here, we show the pool boiler with the sulfur-iodine thermochemical cycle first developed and now being piloted by the General Atomic Company. The tritium (T 2 ) will be generated in the lithium-sodium mixture where the concentration is approx. 10 ppM and held constant by a scavenging system consisting mainly of permeators. An intermediate sodium loop carries the blanket heat to the thermochemical cycle, and the T 2 in this loop is held to 1 ppM by a similar scavenging system. With this design, we have maintained blanket inventory at 1 kg of tritium, kept thermochemical cycle losses to 5 Ci/d and environmental loss to 10 Ci/d, and held total plant risk inventory at 7 kg tritium

Performance of a mass spectrometer for determining low tritium levels from 3He/4He measurements

International Nuclear Information System (INIS)

Lynch, M.C.F.; Kay, D.J.

1981-01-01

The Micromass 3000 mass spectrometer is based on Clarke's 3 He/ 4 He instrument of McMaster University. The principal special features of the MM3000 are: (i) The double collector system, which uses an electron multiplier for the small 3 He + ion beams and a conventional Faraday detector for 4 He + ; (ii) The high sensitivity ion source; and (iii) The low-volume analyser tube employing static vacuum techniques. The sensitivity, resolution and background of the system are designed to permit measurement of 3 He and 4 He levels of the order of 10 -12 cm 3 STP and 10 -6 cm 3 STP, respectively, with a precision of 0.5%, although smaller quantities are detectable. The inherent resolution of the instrument is well in excess of 2000, but a resolution of 600-1000 is normally used for the 3 He + collector as this is sufficient to separate 3 He + from any interfering HD + or H + 3 ions. At this resolution 900 ions per second of 3 He + ions are obtained from 10 -12 cm 3 STP of 3 He. This is the size of 3 He samples obtained from water samples containing tritium at levels around 200 tritium units (1 tritium unit (TU) = IT/10 18 H). At lower tritium levels the 3 He + signal is correspondingly reduced, but the same techniques (described below) allow signals from 1-TU samples (5 ions/s) to be measured with good precision. The limit of detection is reached with quantities of 3 He in the region of 10 -15 cm 3 STP and tritium levels of around 0.1 TU. (author)

[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.

Tritium in a deciduous forest adjacent to a commercial shallow land burial site: implications for monitoring to detect radionuclide migration

International Nuclear Information System (INIS)

Rickard, W.H.; Kirby, L.J.

1983-09-01

Tritium as tritiated water was measured in the sap taken from the trunks of 26 maple trees growing in the vicinity of the shallow-land, low-level radioactive waste disposal site at Maxey Flats, Kentucky. Tritium values ranged between 10,000 and 290,000 pCi/l with the highest levels measured in sap from trees growing downslope from the burial site's western boundary. Levels of tritium of less than 1000 pCi/l were measured at a distance of 20 kilometers from the site: The source of elevated tritium levels in the vicinity of the disposal site is the evaporator facility which has released tritiated water vapor into the air more or less continuously for 10 years. Another possible source of at least some of the tritium is subterranean leakage from the trenches located near the western boundary. The evaporator facility has been shut down since December 1982. With the shutdown of the evaporator the levels of tritium in tree sap in future years is expected to show a marked decline as the tritiated soil water in the root zone becomes increasingly diluted with fresh rainwater and the residual tritium is dissipated to the air by evaporation and plant transpiration processes. 11 references

Detection of tritium sorption on four soil materials

International Nuclear Information System (INIS)

Teng Yanguo; Zuo Rui; Wang Jinsheng; Hu Qinhong; Sun Zongjian; Zeng Ni

2011-01-01

In order to measure groundwater age and design nuclear waste disposal sites, it is important to understand the sorption behavior of tritium on soils. In this study, batch tests were carried out using four soils from China: silty clays from An County and Jiangyou County in Sichuan Province, both of which could be considered candidate sites for Very Low Level Waste disposal; silty sand from Beijing; and loess from Yuci County in Shanxi Province, a typical Chinese loess region. The experimental results indicated that in these soil media, the distribution coefficient of tritium is slightly influenced by adsorption time, water/solid ratio, initial tritium specific activity, pH, and the content of humic and fulvic acids. The average distribution coefficient from all of these influencing factors was about 0.1-0.2 mL/g for the four types of soil samples. This relatively modest sorption of tritium in soils needs to be considered in fate and transport studies of tritium in the environment. - Research highlights: → In this study, batch sorption tests validate the adsorption of tritium on all of the four tested soil samples collected in China, and the distribution coefficient is found to be non-zero and less than 0.4 mL/g. The experimental results indicated that in these soil media, the distribution coefficient of tritium is slightly influenced by adsorption time, water/solid ratio, initial tritium specific activity, pH, and the content of humic and fulvic acids. This relatively modest sorption of tritium in soils needs to be considered in fate and transport studies of tritium in the environment.

Tritium monitoring in the environment of the French territory

Energy Technology Data Exchange (ETDEWEB)

Leprieur, F.; Roussel-Debet, S.; Pierrard, O.; Tournieux, D.; Boissieux, T.; Caldera-Ideias, P. [Institut de radioprotection et de surete nucleaire (France)

2014-07-01

Introduction: Radioactive releases in the environment from civilian and military nuclear facilities have significantly decreased over the last few decades, except for discharges of tritium which are forecast to increase due to changes in the fuel management in power plants and in the longer term by new tritium-emitting units (fusion reactors). In the aim to perform its radiological monitoring mission throughout the French territory, IRSN uses and develops advanced technology equipment to sample and to analyze tritium in the different environmental compartments. Methodology: IRSN uses bubblers to collect both tritium vapour (HTO) and gaseous tritium (mainly HT) in the air. Another method, developed by IRSN, consists in directly sampling the water vapour in the air by condensing in a cold trap and more recently with passive sampler. In continental and marine surface water, samples are usually collected by automatic water samplers. Instantaneous surface water samples are also collected by grab sample devices. In addition, IRSN conducts animal and plant samples near French nuclear facilities. Natural origin and tritium remaining from testing of nuclear weapons In the atmosphere, the background levels of tritium of 1 to 2 Bq/L measured in water vapour, equivalent to an activity of 0.01 to 0.02 Bq/m{sup 3} of air. In fresh waters, the tritium activity currently ranges between 1 and 3 Bq/L of water. In the marine environment, tritium emitted during nuclear weapon tests has been totally 'diluted' in cosmogenic tritium and concentration levels at the surface have remained around 0.1 to 0.2 Bq/L. In biological matrices, total tritium concentration range from 1 to 3 Bq/kg f.w. with a variable proportion of free and organically bounded forms. Tritium around nuclear facilities: Close to facilities releasing more than 2x10{sup 13} Bq/year of gaseous tritium, higher activity levels, ranging from a few tens to a few hundred Bq/L, are observed in the atmospheric and

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)

Development of a wide-range tritium-concentration detector

International Nuclear Information System (INIS)

Jun, F.; Zhe, L.; Shicheng, L.; Jiangfeng, S.; Deli, L.

2015-01-01

According to the requirements of the tritium related systems of the TBM (Test Blanket Module) for monitoring the on-line tritium concentration, a wide-range tritium-concentration detector has been developed to measure the tritium concentration in the range of 10 4 Bq/ml - 5*10 8 Bq/ml. This detector is combined with a low-memory helium ionization chamber. The weak current signal collected in the ionization chamber is converted to the voltage signal by an I-V converter. The minimum weak current which the detector could be measured is 10 -14 A. The performance of the background current and the current response linearity of the prototype have been tested. The test result indicates that the linear response of the current signal of the prototype without connecting the ionization chamber is good. The linear correlation coefficient is R 2 = 0.998

Influence of aging time on residual tritium in Pd beds

International Nuclear Information System (INIS)

Yang Jinshui; Zhang Zhi; Su Yongjun; Jing Wenyong; Du Jie

2012-01-01

The amount of tritium in Pd beds. which were initially loaded at room temperature with tritium at the atomic ratio of T/Pd≈0.65 and aged 1.66 years, 3.47 years and 5.94 years, respectively, was investigated by methods of deuterium exchange, thermal desorption and aqua regia dissolution. Obtained results show that after deuterium exchange and thermal desorption, about 99% of tritium is desorbed from Pd tritide. and the amount of residual tritium become in- creasing significantly as the aged time is increased. which is 3.99 × 10 -7 gT/gPd, 4. 97 × 10 -7 gT/gPd and 1.29 × 10 -6 gT/gPd respectively. The increasing amount of residual tritium could be attributed to the increase of interstitial form of tritium, resulting from increasing interstitial type defects induced by the migration of 3 He atoms in interstitial sites as a function of aged time. (authors)

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

The Use of natural fatty acids in processing tritium gas

International Nuclear Information System (INIS)

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

1997-01-01

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

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

Simulation of tritium behavior after intended tritium release in ventilated room

International Nuclear Information System (INIS)

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

2001-01-01

At the Tritium Process Laboratory (TPL) at the Japan Atomic Energy Research Institute (JAERI), Caisson Assembly for Tritium Safety study (CATS) with 12 m 3 of large airtight vessel (Caisson) was fabricated for confirmation and enhancement of fusion reactor safety to estimate tritium behavior in the case where a tritium leak event should happen. One of the principal objectives of the present studies is the establishment of simulation method to predict the tritium behavior after the tritium leak event should happen in a ventilated room. The RNG model was found to be valid for eddy flow calculation in the 50 m 3 /h ventilated Caisson with acceptable engineering precision. The calculated initial and removal tritium concentration histories after intended tritium release were consistent with the experimental observations in the 50 m 3 /h ventilated Caisson. It is found that the flow near a wall plays an important role for the tritium transport in the ventilated room. On the other hand, tritium behavior intentionally released in the 3,000 m 3 of tritium handling room was investigated experimentally under a US-Japan collaboration. The tritium concentration history calculated with the same method was consistent with the experimental observations, which proves that the present developed method can be applied to the actual scale of tritium handling room. (author)

Tritium 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.

Distribution of tritium in a chronically contaminated lake

International Nuclear Information System (INIS)

Blaylock, B.G.; Frank, M.L.

1978-01-01

White Oak Lake located on the U.S. Department of Energy's Oak Ridge Reservation receives a continuous input of tritium from operating facilities and waste disposal operations at the Oak Ridge National Laboratory. The purpose of this paper was (1) to determine the distribution and concentration of tritium in an aquatic environment which has received releases of tritium significantly greater than expected releases from nuclear power plants, and (2) to determine the effect of fluctuating tritium concentrations in ambient water on the concentration of tritium in fish. Aquatic biota from White Oak Lake were analyzed for tissue water tritium and tissue bound tritium. Except for one plant species, the ratio of tissue water tritium to lake water tritium ranged from 0.80 to 1.02. The tissue water tritium in Gambusia affinis, the mosquito fish, followed closely the significant changes in tritium concentration in lake water. The turnover of tissue water tritium was very rapid; Gambusia from White Oak Lake eliminated 50% of their tissue water tritium in 14 min. The ratio of the specific activity of the tissue bound tritium to the specific activity of the lake water was greatest for the larger species of fish but never exceeded unity. The radiation dose to man from tritium which could be acquired through the aquatic food chain was relatively small when compared to other pathways. The whole body dose to a hypothetical individual taking in concentrations of tritium measured in White Oak Lake was 1.8 mrem/yr from eating fish and 10.0 mrem/yr from drinking water

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.)

Statistical Analysis of Environmental Tritium around Wolsong Site

Energy Technology Data Exchange (ETDEWEB)

Kim, Ju Youl [FNC Technology Co., Yongin (Korea, Republic of)

2010-04-15

To find the relationship among airborne tritium, tritium in rainwater, TFWT (Tissue Free Water Tritium) and TBT (Tissue Bound Tritium), statistical analysis is conducted based on tritium data measured at KHNP employees' house around Wolsong nuclear power plants during 10 years from 1999 to 2008. The results show that tritium in such media exhibits a strong seasonal and annual periodicity. Tritium concentration in rainwater is observed to be highly correlated with TFWT and directly transmitted to TFWT without delay. The response of environmental radioactivity of tritium around Wolsong site is analyzed using time-series technique and non-parametric trend analysis. Tritium in the atmosphere and rainwater is strongly auto-correlated by seasonal and annual periodicity. TFWT concentration in pine needle is proven to be more sensitive to rainfall phenomenon than other weather variables. Non-parametric trend analysis of TFWT concentration within pine needle shows a increasing slope in terms of confidence level of 95%. This study demonstrates a usefulness of time-series and trend analysis for the interpretation of environmental radioactivity relationship with various environmental media.

The development of a versatile field program for measuring tritium in real-time

International Nuclear Information System (INIS)

Rego, J.H.; Smith, D.K.

1994-04-01

Robust sample handling and liquid scintillation counting procedures have been developed to routinely monitor tritium in the field relative to the 20,000 pCi/L drinking water standard. This procedure allows tritium to be monitored hourly during 24 hour drilling operations at depths in the saturated zone potentially contaminated by sub-surface nuclear weapons testing at the Nevada Test Site. Using retrofitted shock hardened and vibration damped counters and strict analytical protocols, tritium may be measured rapidly in the field under hostile conditions. Concentration standards and ''dead'' tritium backgrounds are prepared weekly in a central laboratory and delivered to remote monitoring locations where they are recounted daily as a check on counter efficiency and calibration. Portable counters are located in trailers and powered off a battery pack and line filter fed by mobile generator. Samples are typically ground-waters mixed with drilling fluids returned after circulation through a drill string. Fluids are aerated and ''de-foamed,'' filtered, mixed with scintillation cocktail and subsequently dark-adapted before counting. Besides meeting regulatory requirements, ''real-time'' monitoring affords drilling and field personnel maximum protection against potential exposure to radionuclides; for routine operations, tritium activities may not exceed a 10,000 pCi/L threshold

A rapid and quantitative method to determine the tritium content in DNA from small tissue sampes

International Nuclear Information System (INIS)

Kasche, V.; Zoellner, R.

1979-01-01

A rapid and quantitative two-step procedure to isolate double-strand DNA from small (10-100 mg) animal tissue samples is presented. The method is developed for investigations to evaluate the relative importance of organically bound tritium for the dose factors used to calculate dose commitments due to this nuclide. In the first step the proteins in the homogenized sample are hydrolysed, at a high pH (9.0) and ionic strength (1.5) to dissociate protein from DNA, using immobilized Proteinase K as a proteolytic enzyme. The DNA is then absorbed to hydroxylapatite and separated from impurities by step-wise elution with buffers of increasing ionic strength. More than 90% of the DNA in the samples could be isolated in double-strand form by this procedure. The method has been applied to determine pool-sizes and biological half-life times of tritium in DNA from various animal (mouse) tissues. It has also been shown to be suitable in other radiobiological studies where effects on DNA are investigated. (author)

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

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)

Tritium activities in selected wells on the Nevada Test Site

International Nuclear Information System (INIS)

Lyles, B.F.

1993-05-01

Literature and data were reviewed related to radionuclides in groundwater on and near the Nevada Test Site. No elevated tritium activities have been reported outside of the major testing regions of the Nevada Test Site. Three wells were identified as having water with above-background (>50 pCi/l) tritium activities: UE-15d Water Well; USGS Water Well A; and USGS Test Well B Ex. Although none of these wells have tritium activities greater than the Nevada State Drinking Water standard (20,000 pCi/l), their time-series tritium trends may be indicative to potential on-site radionuclide migration

Development of a wide-range tritium-concentration detector

Energy Technology Data Exchange (ETDEWEB)

Jun, F.; Zhe, L.; Shicheng, L.; Jiangfeng, S.; Deli, L. [China Academy of Engineering Physics, Mianyang (China)

2015-03-15

According to the requirements of the tritium related systems of the TBM (Test Blanket Module) for monitoring the on-line tritium concentration, a wide-range tritium-concentration detector has been developed to measure the tritium concentration in the range of 10{sup 4} Bq/ml - 5*10{sup 8} Bq/ml. This detector is combined with a low-memory helium ionization chamber. The weak current signal collected in the ionization chamber is converted to the voltage signal by an I-V converter. The minimum weak current which the detector could be measured is 10{sup -14} A. The performance of the background current and the current response linearity of the prototype have been tested. The test result indicates that the linear response of the current signal of the prototype without connecting the ionization chamber is good. The linear correlation coefficient is R{sup 2} = 0.998.

Separation setup for the light water detritiation process in the water-hydrogen system based on the membrane contact devices

International Nuclear Information System (INIS)

Rozenkevich, M. B.; Rastunova, I. L.; Prokunin, S. V.

2008-01-01

Detritiation of light water wastes down to a level permissible to discharge into the environment while simultaneously concentrating tritium to decrease amount of waste being buried is a constant problem. The laboratory setup for the light water detritiation process is presented. The separation column consists of 10 horizontally arranged perfluorosulphonic acid Nafion-type membrane contact devises and platinum catalyst (RCTU-3SM). Each contact device has 42.3 cm 2 of the membrane and 10 cm 3 of the catalyst. The column is washed by tritium free light water (L H2O ) and the tritium-containing flow (F HTO ) feeds the electrolyser at λ = G H2 /L H2O = 2. A separation factor of 66 is noted with the device at 336 K and 0.145 MPa. (authors)

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

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.

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)

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

Bioaccumulation factor of tritium in oyster and tilapia

International Nuclear Information System (INIS)

Garcia, T.Y.; Juan, N.B.

1984-01-01

This paper reports on the bioaccumulation factor as well as the residence time of tritium in marine organisms such as tilapia fish (Tilapia mossambica) and oyster (Crassostrea iredalei) reared under laboratory conditions. The organisms were submerged in aquarium water containing tritium with specific activity of 1.0 nCi/ml. The samples were analyzed for tissue-free water tritium (TFWT) by freeze drying and for tissue-bound tritium (TBT) by combustion methods. Tritiated water collected was assayed using the liquid scintillation counting technique. (author)

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

Studies about the transfer phenomena of tritium from liquid to gaseous phase in a catalyst and ordered packing successive system

International Nuclear Information System (INIS)

Bornea, Anisia; Cristescu, Ion; Zamfirache, Marius; Varlam, Carmen

2002-01-01

The processes for hydrogen isotope separation are very important for nuclear technology. One of the most important processes for tritium separation, is the catalyst isotope exchange water-hydrogen. In a column of isotope exchange tritium is transferred from liquid phase (tritiated heavy water) in gaseous phase (hydrogen). In the experimental setup, which was used, the column of catalytic isotope exchange is filled with successive layers of catalyst and ordered packing. The catalyst consists of 95.5 wt.% of PTFE, 4.1 wt. % of carbon and 0.40 wt. % of platinum and was made of Raschig rings 10 x 10 x 2 mm. The ordered packing was of B7 type and consists of a phosphor bronze wire mesh of 0.18 x 0.48 mm dimension. We analysed the transfer phenomena of tritium from liquid to gaseous phase, in this system. The mathematical model presented in the paper allowed computing experimental data for testing the catalyst performances. In this way the speed constants which characterized the isotopic exchange on the catalysis bed ks, and the distillation on the ordered packing kd, were expressed as function of experimental concentrations and hydrodynamic conditions. (authors)

Tritium chemistry in fission and fusion reactors

International Nuclear Information System (INIS)

Roth, E.; Masson, M.; Briec, M.

1986-09-01

We are interested in the behaviour of tritium inside the solids where it is generated both in the case of fission nuclear reactor fuel elements, and in that of blankets of future fusion reactor. In the first case it is desirable to be able to predict whether tritium will be found in the hulls or in the uranium oxide, and under what chemical form, in order to take appropriate steps for it's removal in reprocessing plants. In fusion reactors breeding large amounts of tritium and burning it in the plasma should be accomplished in as short a cycle as possible in order to limit inventories that are associated with huge activities. Mastering the chemistry of every step is therefore essential. Amounts generated are not of the same order of magnitude in the two cases studied. Ternary fissions produce about 66 10 13 Bq (18 000 Ci) per year of tritium in a 1000 MWe fission generator, i.e., about 1.8 10 10 Bq (0.5 Ci) per day per ton of fuel

Cross sections for deuterium, tritium, and helium production in p(bar sign)p collisions at √( s )=1.8 TeV

International Nuclear Information System (INIS)

Alexopoulos, T.; Anderson, E. W.; Biswas, N. N.; Bujak, A.; Carmony, D. D.; Erwin, A. R.; Findeisen, C.; Goshaw, A. T.; Gulbrandsen, K.; Gutay, L. J.

2000-01-01

We present the results of a search for the production of light elements in p(bar sign)p collisions at the Fermilab Tevatron collider. Momentum, time of flight, and dE/dx measurements are used to distinguish nuclei from elementary particles. A production ratio for deuterium to hydrogen is calculated and compared to the primordial value of the big bang model. Some evidence for tritium is found and none for helium isotopes. (c) 2000 The American Physical Society

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

Tritium solubility and permeation in high retention fusion reactor breeder elements

International Nuclear Information System (INIS)

Jakeman, D.

1979-11-01

As an alternative to the current philosophy of reducing the tritium inventory to a minimum by continuously extracting tritium from the breeder of a fusion reactor, an alternative design philosophy is examined in which tritium is contained within high retention breeder elements which can remain in the reactor for a substantial time. To prevent tritium diffusion through the clad of the element it is necessary to maintain a low tritium pressure within the element. Pressures of between 10 4 Pa and 1 Pa appear possible with an element containing a high solubility material provided it is kept below about 400 0 C. This should lead to a leakage into the coolant of between 10 Ci day -1 and 10 4 Ci day -1 which is considerably less than the 10 7 Ci day -1 in present designs. (author)

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

International Nuclear Information System (INIS)

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

2005-01-01

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

On tritium content in the Abramov glacier layers

International Nuclear Information System (INIS)

Voronskaya, G.N.; Nikolishin, I.Ya.; Romanov, V.V.

1976-01-01

Using the common pattern of the analysis of tritium in natural waters its concentration was determined in sampeles of annual layers of the Abramov glacier (Pamir-Altai) at the height of 4500 m above the sea level for 1927-1972. The tritium activity was measured with the help of the liquid scintillation spectrometer with the 10 per cent accuracy. The nature of the obtained curve of the distribution of tritium in the Abramov glacier annual layers was close to its, distribution in glaciers of Greenland, in the Fedchenko glacier and in the precipitation of Teheran. The absolute values of tritium concentrations in the Pamir glaciers are significantly lower than in glaciers of Greenlad. The maximum of tritium concentrations is observed in samples which correspond to 1963, its value approximating to 800 tritium units

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

Tritium and helium behavior in irradiated beryllium

International Nuclear Information System (INIS)

Billone, M.C.; Lin, C.C.; Baldwin, D.L.

1990-11-01

Large quantities of Be (> 100 metric tons) are planned for use in the ITER blanket design to enhance tritium breeding and to act as a thermal barrier between coolant and breeder. Tritium retention/release and He-induced swelling are important issues in blanket design. The data base on tritium and helium behavior in Be is reviewed. New data on tritium retention/release and He bubble growth are presented for Be irradiated to 5 x 10 22 n(E > 1 MeV)/cm 2 at ∼75 degree C and postirradiation-annealed for 700 hours at 500 degree C. A model (diffusion/desorption) is proposed and tested against the data base to determine tritium diffusivity and the desorption rate constant. Similarly a model for He-induced swelling is developed and tested against the data base. The dependence of tritium retention and release on He content and impurities (e.g. BeO) is also explored. 11 refs., 6 figs

Tritium in the DIII-D carbon tiles

International Nuclear Information System (INIS)

Taylor, P.L.; Kellman, A.G.; Lee, R.L.

1993-06-01

The amount of tritium in the carbon tiles used as a first wall in the DIII-D tokamak was measured recently when the tiles were removed and cleaned. The measurements were made as part of the task of developing the appropriate safety procedures for processing of the tiles. The surface tritium concentration on the carbon tiles was surveyed and the total tritium released from tile samples was measured in test bakes. The total tritium in all the carbon tiles at the time the tiles were removed for cleaning is estimated to be 15 mCi and the fraction of tritium retained in the tiles from DIII-D operations has a lower bound of 10%. The tritium was found to be concentrated in a narrow surface layer on the plasma facing side of the tile, was fully released when baked to 1,000 degree C, and was released in the form of tritiated gas (DT) as opposed to tritiated water (DTO) when baked

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.)

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

International Nuclear Information System (INIS)

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

2008-01-01

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

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

Energy Technology Data Exchange (ETDEWEB)

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

2008-10-15

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

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

Science.gov (United States)

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

2008-10-01

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

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.

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

Dependence of CuO particle size and diameter of reaction tubing on tritium recovery for tritium safety operation

Energy Technology Data Exchange (ETDEWEB)

Hu, Cui, E-mail: cdxohc10000@163.com [Shizuoka University, 836 Ohya, Suruga-ku Shizuoka 422-8529 (Japan); Uemura, Yuki; Yuyama, Kenta; Fujita, Hiroe; Sakurada, Shodai; Azuma, Keisuke [Shizuoka University, 836 Ohya, Suruga-ku Shizuoka 422-8529 (Japan); Taguchi, Akira; Hara, Masanori; Hatano, Yuji [University of Toyama, 3190 Gofuku, Toyama 939-8555 (Japan); Chikada, Takumi; Oya, Yasuhisa [Shizuoka University, 836 Ohya, Suruga-ku Shizuoka 422-8529 (Japan)

2016-12-15

Highlights: • Influence of CuO particle size and diameter of reaction tubing on the tritium recovery was evaluated. • Reaction rate constant of tritium with CuO particle has been calculated by the combination of experimental results and a simulation code. • Dependence of reaction tubing length on tritium conversion ratio has been explored. - Abstract: Usage of CuO and water bubbler is one of the conventional and convenient methods for tritium recovery. In present work, influence of CuO particle size and diameter of reaction tubing on the tritium recovery was evaluated. Reaction rate constant of tritium with CuO particle has been calculated by the combination of experimental results and a simulation code. Then, these results were applied for exploring the dependence of reaction tubing length on tritium conversion ratio. The results showed that the surface area of CuO has a great influence on the oxidation rate constant. The frequency factor of the reaction would be approximately doubled by reducing the CuO particle size from 1.0 mm to 0.2 mm. Cross section of reaction tubing mainly affected on the duration of tritium at the temperature below 600 K. Reaction tubing with length of 1 m at temperature of 600 K would be suitable for keeping the tritium conversion ratio above 99.9%. The length of reaction tubing can be reduced by using the smaller CuO particle or increasing the CuO temperature.

Tritium inventory and permeation in the ITER breeding blanket

International Nuclear Information System (INIS)

Violante, V.; Tosti, S.; Sibilia, C.; Felli, F.; Casadio, S.; Alvani, C.

2000-01-01

A model has allowed us to perform the analysis of the tritium inventory and permeation in the international thermonuclear experimental reactor (ITER) breeding blanket under the hypothesis of steady state conditions. Li 2 ZrO 3 (reference) and Li 2 TiO 3 (alternative) have been studied as breeding materials. The total breeder inventory assessed is 7.64 g for the Li 2 ZrO 3 at reference temperature. The model has also been used for a parametric analysis of the tritium permeation. At reference temperature and purge helium velocity of 0.01 m/s, the HT partial pressure is ranging from 10 to 30 Pa in the breeder and 1.5x10 -3 Pa in the beryllium. At 0.1 m/s of purge helium velocity, the HT partial pressure is reduced of one order by magnitude in the breeder and becomes 5x10 -5 Pa in the beryllium. The tritium permeation into the coolant for the whole blanket is ranging from 100 to 250 mCi per day for purge helium velocity of 0.01 m/s. The analysis of the tritium inventory and permeation for the alternative Li 2 TiO 3 breeding material has been carried out too. The tritium inventory in the breeder is in the range from 6 to 375 g larger than in Li 2 ZrO 3 by about a factor 5; the tritium permeation into coolant is comparable to the Li 2 ZrO 3 one. This analysis provides indications on the influence of the operating parameters on the tritium control in the ITER breeding blanket; particularly the control of the tritium inventory by the temperature and the tritium permeation by the purge gas velocity

Tritium saturation in plasma-facing materials surfaces

International Nuclear Information System (INIS)

Longhurst, G.R.; Anderl, R.A.; Pawelko, R.J.; Causey, R.A.; Federici, G.; Haasz, A.A.

1998-01-01

Plasma-facing components in the international thermonuclear experimental reactor (ITER) will experience high heat loads and intense plasma fluxes of order 10 20 -10 23 particles/m 2 s. Experiments on Be and W, two of the materials considered for use in ITER, have revealed that a tritium saturation phenomenon can take place under these conditions in which damage to the surface results that enhances the return of implanted tritium to the plasma and inhibits uptake of tritium. This phenomenon is important because it implies that tritium inventories due to implantation in these plasma-facing materials will probably be lower than was previously estimated using classical recombination-limited release at the plasma surface. Similarly, permeation through these components to the coolant streams should be reduced. In this paper we discuss evidences for the existence of this phenomenon, describe techniques for modeling it, and present results of the application of such modeling to prior experiments. (orig.)

Tritium saturation in plasma-facing materials surfaces

Energy Technology Data Exchange (ETDEWEB)

Longhurst, G.R.; Anderl, R.A.; Pawelko, R.J. [Idaho Nat. Eng. and Environ. Lab., Idaho Falls, ID (United States); Causey, R.A. [Sandia National Labs., Livermore, CA (United States); Federici, G. [ITER Garching Joint Work Site, Garching (Germany); Haasz, A.A. [Toronto Univ., ON (Canada). Inst. for Aerospace Studies

1998-10-01

Plasma-facing components in the international thermonuclear experimental reactor (ITER) will experience high heat loads and intense plasma fluxes of order 10{sup 20}-10{sup 23} particles/m{sup 2}s. Experiments on Be and W, two of the materials considered for use in ITER, have revealed that a tritium saturation phenomenon can take place under these conditions in which damage to the surface results that enhances the return of implanted tritium to the plasma and inhibits uptake of tritium. This phenomenon is important because it implies that tritium inventories due to implantation in these plasma-facing materials will probably be lower than was previously estimated using classical recombination-limited release at the plasma surface. Similarly, permeation through these components to the coolant streams should be reduced. In this paper we discuss evidences for the existence of this phenomenon, describe techniques for modeling it, and present results of the application of such modeling to prior experiments. (orig.) 39 refs.

High efficiency 4H-SiC betavoltaic power sources using tritium radioisotopes

Energy Technology Data Exchange (ETDEWEB)

Thomas, Christopher; Portnoff, Samuel [Widetronix Corp., Ithaca, New York 14850 (United States); Spencer, M. G. [Department of Electrical and Computer Engineering, Cornell University, Ithaca, New York 14850 (United States)

2016-01-04

Realization of an 18.6% efficient 4H-silicon carbide (4H-SiC) large area betavoltaic power source using the radioisotope tritium is reported. A 200 nm 4H-SiC P{sup +}N junction is used to collect high-energy electrons. The electron source is a titanium tritide (TiH{sup 3}{sub x}) foil, or an integrated titanium tritide region formed by the diffusion of tritium into titanium. The specific activity of the source is directly measured. Dark current measured under short circuit conditions was less than 6.1 pA/cm{sup 2}. Samples measured with an external tritium foil produced an open circuit voltage of 2.09 V, short circuit current of 75.47 nA/cm{sup 2}, fill factor of 0.86, and power efficiency of 18.6%. Samples measured with an integrated source produced power efficiencies of 12%. Simulations were done to determine the beta spectrum (modified by self absorption) exiting the source and the electron hole pair generation function in the 4H-SiC. The electron-hole pair generation function in 4H-SiC was modeled as a Gaussian distribution, and a closed form solution of the continuity equation was used to analyze the cell performance. The effective surface recombination velocity in our samples was found to be 10{sup 5}–10{sup 6 }cm/s. Our analysis demonstrated that the surface recombination dominates the performance of a tritium betavoltaic device but that using a thin P{sup +}N junction structure can mitigate some of the negative effects.

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)

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

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.)

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)

Tritium: An analysis of key environmental and dosimetric questions

International Nuclear Information System (INIS)

Till, J.E.; Meyer, H.R.; Etnier, E.L.; Bomar, E.S.; Gentry, R.D.; Killough, G.G.; Rohwer, P.S.; Tennery, V.J.; Travis, C.C.

1980-05-01

This document summarizes new theoretical and experimental data that may affect the assessment of environmental releases of tritium and analyzes the significance of this information in terms of the dose to man. Calculated doses resulting from tritium releases to the environment are linearly dependent upon the quality factor chosen for tritium beta radiation. A reevaluation of the tritium quality factor by the ICRP is needed; a value of 1.7 would seem to be more justifiable than the old 1.0 value. A new exposure model is proposed, based primarily upon the approach recommended by the National Council on Radiation Protection and Measurements. Employing a /open quotes/typical/close quotes/ LMFBR reprocessing facility source term, a /open quotes/base case/close quotes/ dose commitment to total body (for a maximally exposed individual) was calculated to be 4.0 /times/ 10/sup /minus/2/ mSv, with 3.2 /times/ 10/sup /minus// mSv of the dose due to intake of tritium. The study analyzes models which exist for evaluating the buildup of global releases of tritium from man-made sources. Scenarios for the release of man-made tritium to the environment and prediction of collective dose commitment to future generations suggest that the dose from nuclear weapons testing will be less than that from nuclear energy even though the weapons source term is greater than that for any of our energy scenarios

Tritium release from lithium titanate, a low-activation tritium breeding material

International Nuclear Information System (INIS)

Kopasz, J.P.; Miller, J.M.; Johnson, C.E.

1994-01-01

The goals for fusion power are to produce energy in as safe, economical, and environmentally benign a manner as possible. To ensure environmentally sound operation low-activation materials should be used where feasible. The ARIES Tokamak Reactor Study has based reactor designs on the concept of using low-activation materials throughout the fusion reactor. For the tritium breeding blanket, the choices for low activation tritium breeding materials are limited. Lithium titanate is an alternative low-activation ceramic material for use in the tritium breeding blanket. To date, very little work has been done on characterizing the tritium release for lithium titanate. We have thus performed laboratory studies of tritium release from irradiated lithium titanate. The results indicate that tritium is easily removed from lithium titanate at temperatures as low as 600 K. The method of titanate preparation was found to affect the tritium release, and the addition of 0.1% H 2 to the helium purge gas did not improve tritium recovery. ((orig.))

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

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

Conceptual design of an emergency tritium clean-up system

International Nuclear Information System (INIS)

Muller, M.E.

1978-01-01

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

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

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

International Nuclear Information System (INIS)

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

1996-01-01

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

Initial experience of tritium exposure control at JET

International Nuclear Information System (INIS)

Patel, B.; Campling, D.C.; Schofield, P.A.; Macheta, P.; Sandland, K.

1998-01-01

Some of the safety procedures and controls in place for work with tritium are described, and initial operational experience of handling tritium is discussed. A description is given of work to rectify a water leak in a JET neutral beam heating component, which involved man-access to a confined volume to perform repairs, at tritium levels about 100 DAC (80 MBq/m 3 . HTO). Control measures involving use of purge and extract ventilation, and of personal protection using air-fed pressurized suits are described. Results are given of the internal doses to project staff and of atmospheric discharges of tritium during the repair outage. (P.A.)

Tritium burning in inertial electrostatic confinement fusion facility

Energy Technology Data Exchange (ETDEWEB)

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

2016-11-01

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

Tritium burning in inertial electrostatic confinement fusion facility

International Nuclear Information System (INIS)

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

2016-01-01

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

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

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

Estimated yield of double-strand breaks from internal exposure to tritium.

Science.gov (United States)

Chen, Jing

2012-08-01

Internal exposure to tritium may result in DNA lesions. Of those, DNA double-strand breaks (DSBs) are believed to be important. However, experimental and computational data of DSBs induction by tritium are very limited. In this study, microdosimetric characteristics of uniformly distributed tritium were determined in dimensions of critical significance in DNA DSBs. Those characteristics were used to identify other particles comparable to tritium in terms of microscopic energy deposition. The yield of DSBs could be strongly dependent on biological systems and cellular environments. After reviewing theoretically predicted and experimentally determined DSB yields available in the literature for low-energy electrons and high-energy protons of comparable microdosimetric characteristics to tritium in the dimensions relevant to DSBs, it is estimated that the average DSB yields of 2.7 × 10(-11), 0.93 × 10(-11), 2.4 × 10(-11) and 1.6 × 10(-11) DSBs Gy(-1) Da(-1) could be reasonable estimates for tritium in plasmid DNAs, yeast cells, Chinese hamster V79 cells and human fibroblasts, respectively. If a biological system is not specified, the DSB yield from tritium exposure can be estimated as (2.3 ± 0.7) × 10(-11) DSBs Gy(-1) Da(-1), which is a simple average over experimentally determined yields of DSBs for low-energy electrons in various biological systems without considerations of variations caused by different techniques used and obvious differences among different biological systems where the DSB yield was measured.

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

Current CTR-related tritium handling studies at ORNL

International Nuclear Information System (INIS)

Watson, J.S.; Bell, J.T.; Clinton, S.D.; Fisher, P.W.; Redman, J.D.; Smith, F.J.; Talbot, J.B.; Tung, C.P.

1976-01-01

The Oak Ridge National Laboratory has a comprehensive program concerned with plasma fuel recycle, tritium recovery from blankets, and tritium containment in fusion reactors. Two studies of most current interest are investigations of cryosorption pumping of hydrogen isotopes and measurements of tritium permeation rates through steam generator materials. Cryosorption pumping speeds have been measured for hydrogen, deuterium, and helium at pressures from 10 -8 torr to 3 x 10 -3 torr. Permeation rates through Incoloy 800 have been shown to be drastically reduced when the low pressure side of permeation tubes are exposed to steam. These results will be important considerations in the design of fusion reactor steam generators

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

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

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

Ceramic BeO exoelectron dosimeters for tritium and radon monitoring

International Nuclear Information System (INIS)

Gammage, R.B.

1979-01-01

An environmental monitoring device with BeO ceramic dosimeters can be used to measure 222 Rn in dwellings. Radon diffuses into a porous hemispheric chamber and the radon daughters are electrostatically collected on aluminized Mylar foil covering the BeO dosimeter that records the alpha activity. A 10:1 signal-to-background ratio results from a radon exposure of only pCi-h/l. This high sensitivity makes accurate radon measurement possible within one day, even at near background levels of a few tenths pCi/l. The BeO exoelectron dosimeter is also uniquely suited for monitoring occupational exposure to insoluble tritium gas. At one-fifth the maximum permissible concentration, exposure for 8 hours gives a 10:1 signal-to-background exoelectron response to the low energy beta rays. Compensation for any exoelectron response caused by photon radiation can be made by reading the thermoluminescence. The tritium exposure produces negligible thermoluminescence. Progress in these and other applications is now totally dependent on achieving reliability and long-term stability of the exoelectron dosimeter

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

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

Tritium Labelling by Means of Uranium Hydride; Marquage au Tritium au Moyen d'Hydrure d'Uranium; 0414 0435 0447 ; Marcacion con Tritio por Medio de Hidruro de Uranio

Energy Technology Data Exchange (ETDEWEB)

Felter, R. E.; Currie, L. A. [Pennsylvania State University, University Park, PA (United States)

1962-02-15

A new and efficient method for introducing tritium into organic molecules has been observed. Labelling is accomplished by exposure of the organic vapour to heated uranium tritide. In experiments with n-pentane and with ethylene, the principal labelled products were the tritiated parent molecules. The rates of tritium incorporation varied from about 0.2 to 10.0% (of initial tritium) per hour. The mechanism of the reaction has been demonstrated to be not a result of radiation chemistry, but rather a direct reaction of hydrogen atoms from the surface with the hydrocarbon. In addition to the rapid labelling with a significant fraction of the tritium present, the method has another unique advantage : tritium which has not reacted with the organic vapour may be removed from the gas phase simply by cooling the reaction vessel to room temperature. (author) [French] Les auteurs ont mis au point une methode nouvelle et efficace pour introduire le tritium dans les molecules de substances organiques. Le marquage est realise par exposition de la substance organique sous forme de vapeur au tritide Bullet d'uranium chauffe. Dans des experiences avec le n-pe.ntane et l'ethylene, les principaux produits marques ont ete les molecules meres tritiees. Le taux d'incorporation du tritium a varie d'environ 0,2 a 10% (de la quantite initiale de tritium) par heure. On a demontre que le mecanisme de la reaction n'est pas un effet de la chimie des rayonnements, mais plutot une reaction directe des atomes d'hydrogene de la surface avec l'hydrocarbure. Outre qu'une partie importante du tritium utilise reagit rapidement, la methode presente un avantage exceptionnel : on peut aisement separer le tritium qui n'a pas reagi de la substance organique, Bullet en ramenant simplement a la temperature ambiante le recipient dans lequel la reaction a eu lieu. (author) [Spanish] La memoria describe un nuevo procedimiento muy eficaz para introducir tritio en moleculas organicas. La marcacion se consigue

The human body retention time of environmental organically bound Tritium : preliminary analysis of results from a volunteer study

International Nuclear Information System (INIS)

Hunt, John; Bailey, Trevor; Reese, Allan

2008-01-01

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. Preliminary analysis of the results suggests retention of total tritium with body half-times ranging from 4 to 11 days, with no evidence 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 10- 11 Sv Bq -1 may be cautious in this specific situation, and the value of 1.6 10 -11 Sv Bq-1 used by the ICRP for tritiated water might even be more appropriate. 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. (author)

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

Tritium supply assessment for ITER and DEMOnstration power plant

International Nuclear Information System (INIS)

Ni, Muyi; Wang, Yongliang; Yuan, Baoxin; Jiang, Jieqiong; Wu, Yican

2013-01-01

Highlights: • The tritium production rate in CANDU reactor was simulated and estimated. • Possible routes, including APT, CLWR and tritium production schemes of ADS, were evaluated in feasibility and economy. • The possible tritium consumption of ITER and initial supply for DEMO was assessed. • Result of supply and demand showed that after ITER retired in 2038, the tritium production in CANDU reactor might not be enough for a FDS-II scale DEMO reactor startup if without additional tritium resource. -- Abstract: The International Thermonuclear Experimental Reactor (ITER) and next generation DEMOnstration fusion reactor need amounts of tritium for test/initial startup and will consume kilograms tritium for operation per year. The available supply of tritium for fusion reactor is man-made sources. Now most of commercial tritium resource is extracted from moderator and coolant of CANada Deuterium Uranium (CANDU) type Heavy Water Reactor (HWR), in the Ontario Hydro Darlington facility of Canada and Wolsong facility of Korea. In this study, the tritium production rate in CANDU reactor was simulated and estimated. And other possible routes, including Accelerator Production of Tritium (APT), tritium production in Commercial Light Water Reactor (CLWR) and Accelerator Driven Subcritical system (ADS), were also evaluated in feasibility and economy. Based on the tritium requirement investigated according to ITER test schedule and startup inventory required for a FDS-II-scale DEMO calculated by TAS1.0, the assessment results showed that after ITER retired in 2038, the tritium inventory of CANDU reactor could not afford DEMO reactor startup without extra resource

Tritium supply assessment for ITER and DEMOnstration power plant

Energy Technology Data Exchange (ETDEWEB)

Ni, Muyi, E-mail: muyi.ni@fds.org.cn; Wang, Yongliang; Yuan, Baoxin; Jiang, Jieqiong; Wu, Yican

2013-10-15

Highlights: • The tritium production rate in CANDU reactor was simulated and estimated. • Possible routes, including APT, CLWR and tritium production schemes of ADS, were evaluated in feasibility and economy. • The possible tritium consumption of ITER and initial supply for DEMO was assessed. • Result of supply and demand showed that after ITER retired in 2038, the tritium production in CANDU reactor might not be enough for a FDS-II scale DEMO reactor startup if without additional tritium resource. -- Abstract: The International Thermonuclear Experimental Reactor (ITER) and next generation DEMOnstration fusion reactor need amounts of tritium for test/initial startup and will consume kilograms tritium for operation per year. The available supply of tritium for fusion reactor is man-made sources. Now most of commercial tritium resource is extracted from moderator and coolant of CANada Deuterium Uranium (CANDU) type Heavy Water Reactor (HWR), in the Ontario Hydro Darlington facility of Canada and Wolsong facility of Korea. In this study, the tritium production rate in CANDU reactor was simulated and estimated. And other possible routes, including Accelerator Production of Tritium (APT), tritium production in Commercial Light Water Reactor (CLWR) and Accelerator Driven Subcritical system (ADS), were also evaluated in feasibility and economy. Based on the tritium requirement investigated according to ITER test schedule and startup inventory required for a FDS-II-scale DEMO calculated by TAS1.0, the assessment results showed that after ITER retired in 2038, the tritium inventory of CANDU reactor could not afford DEMO reactor startup without extra resource.

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

International Nuclear Information System (INIS)

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

1979-01-01

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

Visual tritium imaging of In-Vessel surfaces

International Nuclear Information System (INIS)

Gentile, C. A.; Zweben, S. J.; Skinner, C. H.; Young, K. M.; Langish, S. W.; Nishi, M. F.; Shu, W. M.; Parker, J.; Isobe, K.

2000-01-01

A imaging detector has been developed for the purpose of providing a non-destructive, real time method of determining tritium concentrations on the surface of internal TFTR vacuum vessel components. The detector employs a green phosphor screen (P31, zinc sulfide: copper) with a wave length peak of 530 nm, a charge-coupled device (CCD) camera linked to a computer, and a detection chamber for inserting components recovered from the vacuum vessel. This detector is capable of determining tritium concentrations on the surfaces. The detector provides a method of imaging tritium deposition on the surfaces in a fairly rapid fashion

Visual tritium imaging of in-vessel surfaces

International Nuclear Information System (INIS)

Gentile, C.A.; Zweben, S.J.; Skinner, C.H.; Young, K.M.; Langish, S.W.; Nishi, M.F.; Shu, W.M.; Parker, J.; Isobe, K.

2000-01-01

An imaging detector has been developed for the purpose of providing a non-destructive, real time method of determining tritium concentrations on the surface of internal TFTR vacuum vessel components. The detector employs a green phosphor screen (P31, zinc sulfide: copper) with a wave length peak of 530 nm, a charge-coupled device (CCD) camera linked to a computer, and a detection chamber for inserting components recovered from the vacuum vessel. This detector is capable of determining tritium concentrations on the surfaces. The detector provides a method of imaging tritium deposition on the surfaces in a fairly rapid fashion

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)

Effluents and releases of tritium from Novo-Voronezh-5 reactor

International Nuclear Information System (INIS)

Babenko, A.G.; Mekhedov, B.N.; Podporinova, L.E.; Popov, S.V.; Shalin, A.N.

1990-01-01

Results of systematic measurements of tritium concentration within technological systems of reactor of Novo-Voronezh NPP conducted to evaluate tritium effluents and releases and radiation doses to population from these effluents and releases are given. It is shown that 68% concerning tritium total amount were disposed into sewerage while 17% - through vent tube and 15% - with water and steam from secondary circuit systems. Standartized tritium effluents from WWER-1000 reactor for 5 year run constitute 15±1.9 GBq/MWxyear and it corresponds to mean value of effluents for foreign NPPs. Tritium concentration in the atmosphere constituted according to calculations (4.1-20)x10 -5 Bq/l. Conclusion is made about insignificant dose to population from tritium gaseous effluents. Detail study is necessary for dose connected with tritium contained in water effluents

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

Mapping of tritium in drinking water from various Indian states

International Nuclear Information System (INIS)

Shah, Chirag A.; Baburajan, A.; Ravi, P.M.; Tripathi, R.M.

2015-01-01

The tritium in fresh water used for drinking purpose across five state of India was analyzed for tritium activity. The tritium data obtained were compared with the monitoring data of tritium in drinking water sources at Tarapur site, which houses a number of nuclear facilities. It is observed that the tritium activity in the water sample from various out station locations were in the range of < 0.48 to 1.33 Bq/l. The tritium value obtained in the drinking water sources at Tarapur was found to be in the range of 0.91 to 3.10 Bq/l. The monitoring of tritium in drinking water from Tarapur and from various out station location indicate that the level is negligible compared to the USEPA limit of 10000 Bq/l and the contribution of operation nuclear facilities to the tritium activity in drinking water source at Tarapur is insignificant. (author)

The hazard to man of accidental releases of tritium

International Nuclear Information System (INIS)

Brearley, I.R.

1985-03-01

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

Concentration of tritium in precipitation and river water

International Nuclear Information System (INIS)

Chatani, Kunio

1983-01-01

The concentration of tritium in precipitation and river water has been measured sice 1973 in Aichi, Japan. The tritium in water samples was enriched by electrolysis, and measured by liquid scintillation counting. The concentration of tritium in precipitation decreased from 27 TU in 1973 to 17 TU in 1979, and showed seasonal variation. During this period, there was a rise of concentration because of Chinese nuclear detonation. The concentration of tritium in river water gradually decreased from 44 TU in 1973 to 24 TU in 1979, and the seasonal variation was not observed. Based on the observed values, the relation among precipitation, river water and ground water was analyzed. (J.P.N.)

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

Studies on steps affecting tritium residence time in solid blanket

International Nuclear Information System (INIS)

Tanaka, Satoru

1987-01-01

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

The releases of krypton-85 and tritium to the environment and tritium to krypton-85 ratios as source indicators

International Nuclear Information System (INIS)

Schroeder, K.J.P.; Roether, W.

1975-01-01

More than 95% of the krypton-85 that is at present observed in the environment on a global scale originates from the combined releases following nuclear-power generation and plutonium production, while atmospheric fusion-bomb testing accounts for the same percentage of the global tritium. The global inventories at the end of 1973 were 55 MCi (estimated uncertainty +- 10%) of krypton-85, and 2900 MCi (+- 25%) of tritium. From the excess of the global krypton-85 inventory over the amounts accounted for by the sources other than plutonium production, it is concluded that 130 tonnes of plutonium-239 have been produced up to 1970. Pronounced fractionation occurs between atmosphere and hydrosphere, in the sense that the concentration of krypton-85 is lowered, and that of tritium (being overwhelmingly in the form of a water molecule, HTO) is greatly increased, in the hydrosphere. Largely as a consequence of this fractionation, the environmental tritium to krypton-85 ratios cover a wide range, with values lowest in the troposphere (typical order of magnitude 10 -1 Ci/Ci) and highest in continental surface water (of the order of 10 5 ). Preliminary oceanic krypton-85 data are reported, which indicate that the concentration decrease with depth in the ocean is very similar for both nuclides. Effluents from nuclear power reactors and reprocessing plants have tritium to krypton-85 ratios that do not differ markedly from those found at present in the troposphere; on the other hand, the very high ratios that are typical of the hydrosphere may offer opportunities of detecting such effluents in the hydrosphere on the basis of tritium to krypton-85 ratios. Considerable uncertainties in the ratios of the effluents have, however, to be anticipated, arising from varying, and fluctuating, fractionation between the two nuclides in the release processes. (author)

Behavior of environmental carbon-14 and tritium in Japan

International Nuclear Information System (INIS)

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

1979-01-01

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

Design study of fuel circulating system using Pd alloy membrane isotope separation method

International Nuclear Information System (INIS)

Naito, T.; Yamada, T.; Aizawa, T.; Kasahara, T.; Yamanaka, T.

1981-01-01

It is expected that the method of permeating through Pd-alloy membrances is effective for isotope separation and the refining of fuel gas. In this paper, the design study of the Fuel Circulating System (FCS) using Pb-alloy membranes is described. The study is mainly focused on the main vacuum, fuel gas refining, isotope separating, and tritium containment systems. In the fuel gas refining system, impurities are effectively removed by using Pd-alloy membranes. For the isotope separation system, the diffusion method through Pd-alloy membranes was adopted. From the standpoint of the safety and economy, a three-stage tritium containment system was adopted to control tritium release to the environment as low as possible. The principal conclusion drawn from the design study was as follows. In the FCS, while cryogenic distillation method appears to be practicable, Pd-alloy membrane method is attractive for isotope separation and the refining of fuel gas. For a large amount of tritium inventory, handling and control technologies should be completed by the experimental evaluation and development of the components and materials used for the FCS. A three-stage containment system was adopted to control tritium release to environment as low as possible. Consideration to prevent tritium escape will be necessary for fuel gas refiners and isotope separators. (Kato, T.)

Levels of tritium concentration in the environmental samples around JAERI TOKAI

International Nuclear Information System (INIS)

Matsuura, K.; Sasa, Y.; Nakamura, C.; Katagiri, H.

1995-01-01

By the operation of research reactors, tritium-handling facilities, nuclear power plants, and a reprocessing facility around JAERI TOKAI, tritium is released into the environment in compliance with the regulatory standards. To investigate the levels of tritium concentration in environmental samples around JAERI, rain, air (vapor and hydrogen gas), and tissue-free water of pine needles were measured and analyzed from 1984 to 1993. Sampling locations were determined by taking into consideration wind direction, distance from nuclear facilities, and population distribution. The NAKA site (about 6 km west-northwest from the Tokai site) was also selected as a reference point. Rain and tissue-free water of pine needles were sampled monthly. For air samples, sampling was carried out for two weeks by using the continuous tritium sampler. After the pretreatment of samples, tritium concentrations were measured by a low background liquid scintillation counter (detection limit 0.8 Bq/l). Annual mean tritium concentrations in rain observed at six points for 10 years was 0.8 to 8.9 Bq/l, which decreased with distance from the nuclear facilities. Tritium concentrations in rain obtained at Chiba City were around 0.8 Bq/l (1987-1988) and those at the NAKA site were 0.8 to 3.8 Bq/l. Annual mean HTO concentrations in air at three points for 10 years were 9.2 x 10 -2 to 1.1 Bq/m 3 , although HT concentrations in air, ranging from 1.7 x 10 -2 to 5.8 x 10 -2 Bq/m 3 , were not influenced by the operation of the nuclear facilities. Annual mean tritium concentrations in tissue-free water of pine needles at four points for 10 years were 1.4 to 31 Bq/l. Those at the NAKA site ranging from 1.4 to 6.2 Bq/l were in good agreement with the reported value by Takashima of 0.78 to 3.0 Bq/l at twenty-one locations in Japan. Monthly mean HTO concentrations in air for 10 years showed a good correlation with absolute humidity, while other samples showed no seasonal variation. Higher level tritium

Estimated yield of double-strand breaks from internal exposure to tritium

Energy Technology Data Exchange (ETDEWEB)

Chen, Jing [Health Canada, Radiation Protection Bureau, Ottawa, ON (Canada)

2012-08-15

Internal exposure to tritium may result in DNA lesions. Of those, DNA double-strand breaks (DSBs) are believed to be important. However, experimental and computational data of DSBs induction by tritium are very limited. In this study, microdosimetric characteristics of uniformly distributed tritium were determined in dimensions of critical significance in DNA DSBs. Those characteristics were used to identify other particles comparable to tritium in terms of microscopic energy deposition. The yield of DSBs could be strongly dependent on biological systems and cellular environments. After reviewing theoretically predicted and experimentally determined DSB yields available in the literature for low-energy electrons and high-energy protons of comparable microdosimetric characteristics to tritium in the dimensions relevant to DSBs, it is estimated that the average DSB yields of 2.7 x 10{sup -11}, 0.93 x 10{sup -11}, 2.4 x 10{sup -11} and 1.6 x 10{sup -11} DSBs Gy{sup -1} Da{sup -1} could be reasonable estimates for tritium in plasmid DNAs, yeast cells, Chinese hamster V79 cells and human fibroblasts, respectively. If a biological system is not specified, the DSB yield from tritium exposure can be estimated as (2.3 ± 0.7) x 10{sup -11} DSBs Gy{sup -1} Da{sup -1}, which is a simple average over experimentally determined yields of DSBs for low-energy electrons in various biological systems without considerations of variations caused by different techniques used and obvious differences among different biological systems where the DSB yield was measured. (orig.)

Tritium levels in milk in the vicinity of chronic tritium releases

International Nuclear Information System (INIS)

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

2016-01-01

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

Conversion of tritium gas to tritiated water in the environment

International Nuclear Information System (INIS)

Noguchi, Hiroshi; Kato, Shohei

1985-01-01

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

Tritium Research Laboratory safety analysis report

Energy Technology Data Exchange (ETDEWEB)

Wright, D.A.

1979-03-01

Design and operational philosophy has been evolved to keep radiation exposures to personnel and radiation releases to the environment as low as reasonably achievable. Each experiment will be doubly contained in a glove box and will be limited to 10 grams of tritium gas. Specially designed solid-hydride storage beds may be used to store temporarily up to 25 grams of tritium in the form of tritides. To evaluate possible risks to the public or the environment, a review of the Sandia Laboratories Livermore (SLL) site was carried out. Considered were location, population, land use, meteorology, hydrology, geology, and seismology. The risks and the extent of damage to the TRL and vital systems were evaluated for flooding, lightning, severe winds, earthquakes, explosions, and fires. All of the natural phenomena and human error accidents were considered credible, although the extent of potential damage varied. However, rather than address the myriad of specific individual consequences of each accident scenario, a worst-case tritium release caused indirectly by an unspecified natural phenomenon or human error was evaluated. The maximum credible radiological accident is postulated to result from the release of the maximum quantity of gas from one experiment. Thus 10 grams of tritium gas was used in the analysis to conservatively estimate the maximum whole-body dose of 1 rem at the site boundary and a maximum population dose of 600 man-rem. Accidental release of this amount of tritium implies simultaneous failure of two doubly contained systems, an occurrence considered not credible. Nuclear criticality is impossible in this facility. Based upon the analyses performed for this report, we conclude that the Tritium Research Laboratory can be operated without undue risk to employees, the general public, or the environment. (ERB)

Tritium Research Laboratory safety analysis report

International Nuclear Information System (INIS)

Wright, D.A.

1979-03-01

Design and operational philosophy has been evolved to keep radiation exposures to personnel and radiation releases to the environment as low as reasonably achievable. Each experiment will be doubly contained in a glove box and will be limited to 10 grams of tritium gas. Specially designed solid-hydride storage beds may be used to store temporarily up to 25 grams of tritium in the form of tritides. To evaluate possible risks to the public or the environment, a review of the Sandia Laboratories Livermore (SLL) site was carried out. Considered were location, population, land use, meteorology, hydrology, geology, and seismology. The risks and the extent of damage to the TRL and vital systems were evaluated for flooding, lightning, severe winds, earthquakes, explosions, and fires. All of the natural phenomena and human error accidents were considered credible, although the extent of potential damage varied. However, rather than address the myriad of specific individual consequences of each accident scenario, a worst-case tritium release caused indirectly by an unspecified natural phenomenon or human error was evaluated. The maximum credible radiological accident is postulated to result from the release of the maximum quantity of gas from one experiment. Thus 10 grams of tritium gas was used in the analysis to conservatively estimate the maximum whole-body dose of 1 rem at the site boundary and a maximum population dose of 600 man-rem. Accidental release of this amount of tritium implies simultaneous failure of two doubly contained systems, an occurrence considered not credible. Nuclear criticality is impossible in this facility. Based upon the analyses performed for this report, we conclude that the Tritium Research Laboratory can be operated without undue risk to employees, the general public, or the environment

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

Cellular- and micro-dosimetry of heterogeneously distributed tritium.

Science.gov (United States)

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

2012-01-01

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

TFTR tritium handling concepts

International Nuclear Information System (INIS)

Garber, H.J.

1976-01-01

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

JET experiments with tritium and deuterium–tritium mixtures

Energy Technology Data Exchange (ETDEWEB)

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

2016-11-01

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

Sources of tritium

International Nuclear Information System (INIS)

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

1980-12-01

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

Separation of tritiated water using graphene oxide membrane

Energy Technology Data Exchange (ETDEWEB)

Sevigny, Gary J. [Pacific Northwest National Laboratory (PNNL), Richland, WA (United States); Motkuri, Radha K. [Pacific Northwest National Laboratory (PNNL), Richland, WA (United States); Gotthold, David W. [Pacific Northwest National Laboratory (PNNL), Richland, WA (United States); Fifield, Leonard S. [Pacific Northwest National Laboratory (PNNL), Richland, WA (United States); Frost, Anthony P. [Pacific Northwest National Laboratory (PNNL), Richland, WA (United States); Bratton, Wesley [Pacific Northwest National Laboratory (PNNL), Richland, WA (United States)

2015-06-28

In future nuclear fuel reprocessing plants and possibly for nuclear power plants, the cleanup of tritiated water will be needed for hundreds of thousands of gallons of water with low activities of tritium. This cleanup concept utilizes graphene oxide laminar membranes (GOx) for the separation of low-concentration (10-3-10 µCi/g) tritiated water to create water that can be released to the environment and a much smaller waste stream with higher tritium concentrations. Graphene oxide membranes consist of hierarchically stacked, overlapping molecular layers and represent a new class of materials. A permeation rate test was performed with a 2-µm-thick cast Asbury membrane using mixed gas permeability testing with zero air (highly purified atmosphere) and with air humidified with either H2O or D2O to a nominal 50% relative humidity. The membrane permeability for both H2O and D2O was high with N2 and O2 at the system measurement limit. The membrane water permeation rate was compared to a Nafion® membrane and the GOx permeation was approximately twice as high at room temperature. The H2O vapor permeation rate was 5.9 × 102 cc/m2/min (1.2 × 10-6 g/min-cm2), which is typical for graphene oxide membranes. To demonstrate the feasibility of such isotopic water separation through GOX laminar membranes, an experimental setup was constructed to use pressure-driven separation by heating the isotopic water mixture at one side of the membrane to create steam while cooling the other side. Several membranes were tested and were prepared using different starting materials and by different pretreatment methods. The average separation result was 0.8 for deuterium and 0.6 for tritium. Higher or lower temperatures may also improve separation efficiency but neither has been tested yet. A rough estimate of cost compared to current technology was also included as an indication of potential viability of the process. The relative process costs were based on the rough size of facility to

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

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.

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

International Nuclear Information System (INIS)

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

1988-01-01

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

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

International Nuclear Information System (INIS)

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

1988-01-01

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

Tritium contaminated waste management at the tritium systems test assembly

International Nuclear Information System (INIS)

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

1987-01-01

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

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)

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.

In-vessel tritium

International Nuclear Information System (INIS)

Ueda, Yoshio; Ohya, Kaoru; Ashikawa, Naoko; Ito, Atsushi M.; Kato, Daiji; Kawamura, Gakushi; Takayama, Arimichi; Tomita, Yukihiro; Nakamura, Hiroaki; Ono, Tadayoshi; Kawashima, Hisato; Shimizu, Katsuhiro; Takizuka, Tomonori; Nakano, Tomohide; Nakamura, Makoto; Hoshino, Kazuo; Kenmotsu, Takahiro; Wada, Motoi; Saito, Seiki; Takagi, Ikuji; Tanaka, Yasunori; Tanabe, Tetsuo; Yoshida, Masafumi; Toma, Mitsunori; Hatayama, Akiyoshi; Homma, Yuki; Tolstikhina, Inga Yu.

2012-01-01

The in-vessel tritium research is closely related to the plasma-materials interaction. It deals with the edge-plasma-wall interaction, the wall erosion, transport and re-deposition of neutral particles and the effect of neutral particles on the fuel recycling. Since the in-vessel tritium shows a complex nonlinear behavior, there remain many unsolved problems. So far, behaviors of in-vessel tritium have been investigated by two groups A01 and A02. The A01 group performed experiments on accumulation and recovery of tritium in thermonuclear fusion reactors and the A02 group studied theory and simulation on the in-vessel tritium behavior. In the present article, outcomes of the research are reviewed. (author)

Tritium transfer studies in cellulose-HTO system

International Nuclear Information System (INIS)

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

1986-01-01

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

Tritium monitoring at the Sandia Tritium Research Laboratory

International Nuclear Information System (INIS)

Devlin, T.K.

1978-10-01

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

Tritium 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

Irradiation of lithium aluminate and tritium extraction

International Nuclear Information System (INIS)

Roth, E.; Abassin, J.J.; Botter, F.; Briec, M.; Chenebault, P.; Masson, M.; Rasneur, B.; Roux, N.

1984-12-01

After preselection of the preparation procedures, following short irradiations, γ LiAl0 2 samples submitted to 2.10 19 fast neutrons cm -2 and 1.5 10 20 thermal neutrons cm -2 fluences experienced no apparent damage. Post-irradiation tritium extraction from samples irradiated to 2.10 17 neutrons/cm 2 in quartz ampoules produced mostly tritiated water. When in-pile experiments are performed the sample container material influences greatly the measured ratio of tritium gas to tritiated water - Stainless steel capsules yield more T 2 gas than quartz capsules probably because of a reduction process. Difficulties in interpretation arise from adsoption of tritiated water on the measuring lines. Both experiments showed that much faster extraction rates are obtained from small grain size samples than from large ones at the same open porosity. If diffusion in the grains controls the extraction rates, apparent D values vary from 10 -16 to 1.5 10 -15 cm 2 S -1 in the temperature range explored. Around 500 0 C small grain samples reached equilibrium tritium concentration of a few mCi in 4 hours. Such values are suitable for a blanket concept

Tritium content in tissue free water of Japanese bodies

Energy Technology Data Exchange (ETDEWEB)

Ujeno, Y.; Yamamoto, K.; Aoki, T.; Kurihara, N.

1986-01-01

The tritium content of tissue free water was measured in fresh, non-diseased organs (brain, lungs, liver, kidneys and muscle) removed by forensic autopsy from 4 male and 4 female bodies. Tissue free water was extracted by freeze drying and distillation and tritium measured in the absence of background radon gas. A typical count was approximately 2.70 cpm. The mean tritium content of tissue free water in all the organs examined was 2.50 + - 0.67 Bq.1/sup -1/ (67.6 + -18.2 pCi1/sup -1/). This value was much lower than that obtained for tissues from Italian bodies: the value was, however, similar to that obtained for tap water (70.2 + -28.0 pCi.1/sup -1/), rain water (77.8 + - 47.4 pCi.1/sup -1/) and tissue free water of foods (55.6 + - 26.2 pCi.1/sup -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)

Tritium technology. A Canadian overview

Energy Technology Data Exchange (ETDEWEB)

Hemmings, R.L. [Canatom NPM (Canada)

2002-10-01

An overview of the various tritium research and operational activities in Canada is presented. These activities encompass tritium processing and recovery, tritium interactions with materials, and tritium health and safety. Many of these on-going activities form a sound basis for the tritium use and handling aspects of the ITER project. Tritium management within the CANDU heavy water reactor, associated detritiation facilities, research and development facilities, and commercial industry and improving the understanding of tritium behaviour in humans and the environment remain the focus of a long-standing Canadian interest in tritium. While there have been changes in the application of this knowledge and experience over time, the operating experience and the supporting research and development continue to provide for improved plant and facility operations, an improved understanding of tritium safety issues, and improved products and tools that facilitate tritium management. (author)

Tritium technology. A Canadian overview

International Nuclear Information System (INIS)

Hemmings, R.L.

2002-01-01

An overview of the various tritium research and operational activities in Canada is presented. These activities encompass tritium processing and recovery, tritium interactions with materials, and tritium health and safety. Many of these on-going activities form a sound basis for the tritium use and handling aspects of the ITER project. Tritium management within the CANDU heavy water reactor, associated detritiation facilities, research and development facilities, and commercial industry and improving the understanding of tritium behaviour in humans and the environment remain the focus of a long-standing Canadian interest in tritium. While there have been changes in the application of this knowledge and experience over time, the operating experience and the supporting research and development continue to provide for improved plant and facility operations, an improved understanding of tritium safety issues, and improved products and tools that facilitate tritium management. (author)

Hydrogen isotope separation by cryogenic distillation method

International Nuclear Information System (INIS)

Hayakawa, Nobuo; Mitsui, Jin

1987-01-01

Hydrogen isotope separation in fusion fuel cycle and tritium recovery from heavy water reactor are very important, and therefore the early establishment of these separation techniques are desired. The cryogenic distillation method in particular is promising for the separation of hydrogen isotope and the recovery of high concentrated tritium. The studies of hydrogen isotope separation by cryogenic distillation method have been carried out by using the experimental apparatus made for the first time in Japan. The separation of three components (H 2 -HD-D 2 ) under total reflux conditions was got by using the packing tower of 500 mm height. It was confirmed that the Height Equivalent Theoretical Plate (HETP) was 20 - 30 mm for the vapor's line velocity of 20 - 80 mm/s. (author)

Tritium

International Nuclear Information System (INIS)

Fiege, A.

1992-07-01

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

Tritium contamination in [18O] water containing 18F produced by a cyclotron

International Nuclear Information System (INIS)

Ito, S.; Saze, T.; Sakane, H.; Nishizawa, K.

2003-01-01

Tritium in the target [ 18 O] water irradiated with 9.6 MeV protons for producing [ 18 F] fluoride by 18 O(p, n) 18 F reaction was predicted from the consideration on the Q value of the 18 O(p, t) 16 O reaction. A tritium beta ray spectrum was measured by a liquid scintillation counter equipped with a multichannel analyzer. The ratio of the 3 H activity to the 18 F activity in the [ 18 O] target water was 2.4x10 -6 at the beam current of 25μA. Tritium also was detected in the [ 18 O] water for recycling and the wasted acetonitrile [ 18 O] water. The purified [ 18 F]-FDG solution was not contaminated by 3 H. The 40% 3 H out of the produced activity was lost in the course of the [ 18 F]-FDG synthesis. It was suggested that 3 H evaporated into the air during [ 18 F]-FDG synthesis and caused contamination of the workroom. The radiation workers should be prevented from environmental 3 H contamination. (author)

Measurement of the tritium concentration in the fractionated distillate from environmental water samples.

Science.gov (United States)

Atkinson, Robert; Eddy, Teresa; Kuhne, Wendy; Jannik, Tim; Brandl, Alexander

2014-09-01

Standard procedures for the measurement of tritium in water samples often require distillation of an appropriate sample aliquot. This distillation process may result in a fractionation of tritiated water and regular light water due to the vapor pressure isotope effect, introducing either a bias or an additional contribution to the total tritium measurement uncertainty. The current study investigates the relative change in vapor pressure isotope effect in the course of the distillation process, distinguishing it from and extending previously published measurements. The separation factor as a quantitative measure of the vapor pressure isotope effect is found to assume values of 1.04 ± 0.036, 1.05 ± 0.026, and 1.07 ± 0.038, depending on the vigor of the boiling process during distillation of the sample. A lower heat setting in the experimental setup, and therefore a less vigorous boiling process, results in a larger value for the separation factor. For a tritium measurement in water samples where the first 5 mL are discarded, the tritium concentration could be underestimated by 4-7%. Copyright © 2014 Elsevier Ltd. All rights reserved.

In-pile test of tritium recovery from lithium oxide

International Nuclear Information System (INIS)

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

1984-05-01

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

A 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.

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

Tritium safety study using Caisson Assembly (CATS) at TPL/JAEA

International Nuclear Information System (INIS)

Hayashi, T.; Kobayashi, K.; Iwai, Y.; Isobe, K.; Nakamura, H.; Kawamura, Y.; Shu, W.; Suzuki, T.; Yamada, M.; Yamanishi, T.

2008-01-01

Tritium confinement is required as the most important safety Junction for a fusion reactor. In order to demonstrate the confinement performance experimentally, an unique equipment, called CATS: Caisson Assembly for Tritium Safety study, was installed in Tritium Process Laboratory of Japan Atomic Energy Agency and operated for about 10 years. Tritium confinement and migration data in CATS have been accumulated and dynamic simulation code was accumulated using these data. Contamination and decontamination behavior on various materials and new safety equipment functions have been investigated under collaborations with a lot of laboratories and universities. (authors)

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

Measurements of tritium recycling and isotope exchange in TFTR

International Nuclear Information System (INIS)

Skinner, C.H.; Kamperschroer, J.; Mueller, D.; Nagy, A.; Stotler, D.P.

1996-05-01

Tritium Balmer-alpha (T α ) emission, along with H α and D α is observed in the current D-T experimental campaign in TFTR. The data are a measure of the fueling of the plasma by tritium accumulated in the TFTR limiter and the spectral profile maps neutral hydrogenic velocities. T α is relatively slow to appear in tritium neutral beam heated discharges, (T α /(H α + D α + T α ) = 11% after 8 tritium-only neutral beam discharges). In contrast, the T α fraction in a sequence of six discharges fueled with tritium puff,s increased to 44%. Larger transient increases (up to 75% T α ) were observed during subsequent tritium gas puffs. Analysis of the Doppler broadened spectral profiles revealed overall agreement with the dissociation, charge exchange, sputtering and reflection velocities predicted by the neutral Monte-Carlo code DEGAS with some deficiency in the treatment of dissociation products in the 10--100 eV range

Tritium control: October 1982-March 1983

International Nuclear Information System (INIS)

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

1983-01-01

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

Using the Tritium Plasma Experiment to evaluate ITER PFC safety

International Nuclear Information System (INIS)

Longhurst, G.R.; Anderl, R.A.; Bartlit, J.R.; Causey, R.A.; Haines, J.R.

1993-01-01

The Tritium Plasma Experiment was assembled at Sandia National Labs., Livermore and is being moved to the Tritium Systems Test Assembly facility at Los Alamos National Lab. to investigate interactions between dense plasmas at low energies and plasma-facing component materials. This apparatus has the unique capability of replicating plasma conditions in a tokamak divertor with particle flux densities of 2 x 10 23 ions/m 2 .s and a plasma temperature of about 15 eV using a plasma that includes tritium. An experimental program has been initiated using the Tritium Plasma Experiment to examine safety issues related to tritium in plasma-facing components, particularly the ITER divertor. Those issues include tritium retention and release characteristics, tritium permeation rates and transient times to coolant streams, surface modification and erosion by the plasma, the effects of thermal loads and cycling, and particulate production. An industrial consortium led by McDonnell Douglas will design and fabricate the test fixtures

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

Science.gov (United States)

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

2016-01-01

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

On the conversion of tritium units to mass fractions for hydrologic applications.

Science.gov (United States)

Stonestrom, David A; Andraski, Brian J; Cooper, Clay A; Mayers, C Justin; Michel, Robert L

2013-06-01

We develop a general equation for converting laboratory-reported tritium levels, expressed either as concentrations (tritium isotope number fractions) or mass-based specific activities, to mass fractions in aqueous systems. Assuming that all tritium is in the form of monotritiated water simplifies the derivation and is shown to be reasonable for most environmental settings encountered in practice. The general equation is nonlinear. For tritium concentrations c less than 4.5 × 10(12) tritium units (TU) - i.e. specific tritium activitiesconversion is linear for all practical purposes. Terrestrial abundances serve as a proxy for non-tritium isotopes in the absence of sample-specific data. Variation in the relative abundances of non-tritium isotopes in the terrestrial hydrosphere produces a minimum range for the mantissa of the conversion factor of [2.22287; 2.22300].

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)

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

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

Science.gov (United States)

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

2017-11-01

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

The measurement of tritium in water samples with electrolytic enrichment using liquid scintillation counter

Directory of Open Access Journals (Sweden)

Janković Marija M.

2012-01-01

Full Text Available Tritium (3H present in the environment decreased in the last decades and nowadays it has low activity concentrations. Measurement of low-level tritium activities in natural waters, e. g. in precipitation, groundwater, and river water requires special techniques for water pretreatment and detection of low-level radioactivity. In order to increase the tritium concentration to an easily measurable level, electrolytic enrichment must be applied. This paper presents the enrichment method performed by electrolysis in a battery of 18 cells, giving an enrichment factor of 5.84 (calculated from 59 electrolyses. The calculated mean values of the separation factor and enrichment parameter were 4.10 and 0.84, respectively. Results for tritium activity in precipitation and surface water collected in Belgrade during 2008 and 2009 are presented. The Radiation and Environmental Protection Department of the Vinča Institute of Nuclear Sciences, participated in the IAEA TRIC2008 international intercomparison exercise. The participation in the intercomparisons for any laboratory doing low-level 3H measurements in the waters is very important and useful. It is considered the best way to check the entire procedure and methods of the measurements and the reliability of the standard used. The analysis of the reported 3H activity results showed that all results for five intercomparison samples, for which electrolytic enrichment were applied prior to the 3H measurement, are acceptable.

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)

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)

Research and development of lithium isotope separation using an ionic-liquid impregnated organic membrane

International Nuclear Information System (INIS)

Hoshino, Tsuyoshi

2013-01-01

The tritium needed as a fuel for fusion reactors is produced by the neutron capture reaction of lithium-6 ( 6 Li) in tritium breeding materials. However, natural Li contains only about 7.6 at.% 6 Li. In Japan, new lithium isotope separation technique using ionic-liquid impregnated organic membranes have been developed. The improvement in the durability of the ionic-liquid impregnated organic membrane is one of the main issues for stable, long-term operation of electrodialysis cells while maintaining good performance. Therefore, we developed highly-durable ionic-liquid impregnated organic membrane. Both ends of the ionic-liquid impregnated organic membrane were covered by a nafion 324 overcoat to prevent the outflow of the ionic liquid. The transmission of Lithium aqueous solution after 10 hours under the highly-durable ionic-liquid impregnated organic membrane is almost 13%. So this highly-durable ionic-liquid impregnated organic membrane for long operating of electrodialysis cells has been developed through successful prevention of ion liquid dissolution. (J.P.N.)

Tritium in nuclear power plants

International Nuclear Information System (INIS)

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

1981-01-01

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

Environmental aspects of tritium

International Nuclear Information System (INIS)

Quisenberry, D.R.

1979-01-01

The potential radiological implications of environmental tritium releases must be determined in order to develop a programme for dealing with the tritium inventory predicted for the nuclear power industry which, though still in its infancy, produces tritium in megacurie quantities annually. Should the development of fusion power generation become a reality, it will create a potential source for large releases of tritium, much of it in the gaseous state. At present about 90% of the tritium produced enters the environment through gaseous and liquid effluents and is deposited in the hydrosphere as tritiated water. Tritium can be assimilated by plants and animals and organically bound, regardless of the exposure pathway. However, there appears to be no concentration factor relative to hydrogen at any level of food chains analysed to date. The body burden, for man, is dependent on the exposure pathway and tissue-bound fractions are primarily the result of organically bound tritium in food. (author)

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.

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)

Tritium in the Savannah River Estuary and adjacent marine waters

International Nuclear Information System (INIS)

Hayes, D.W.

1978-01-01

The tritium distribution in the Savannah River estuary and adjacent marine waters was measured to provide information on the dilution, mixing, and movement of Savannah River water in this region. The Savannah River marine region was chosen because the average tritium concentration in this river is 5 pCi/ml, whereas other rivers in the southeastern United States average less than 0.5 pCi/ml. The increased tritium concentration in the Savannah River is due to releases from the Savannah River Plant of the Department of Energy. Tritium measurements have proved particularly effective in estimating the flushing time of the Savannah River estuary (2.4 days) and in delineating the relative contribution to the water masses in Ossabaw and Port Royal Sounds from the River and from sea water. Ossabaw and Port Royal Sounds are located approximately 20 km south and north of the Savannah River estuary, respectively

Tritium contamination and monitoring at Frascati Neutron Generator

Energy Technology Data Exchange (ETDEWEB)

Lucci, F.; Sandri, S.; Ianni, A. [ENEA, Frascati (Italy). Dipartimento Ambiente; Vasselli, R. [ANPA, Roma (Italy); Pillon, M.; Bettinali, L. [ENEA, Frascati (Italy). Dipartimento Energia

1994-11-01

The Frascati Neutron Generator (FGN) is a specialised 300 keV, 3 mA direct electrostatic deuteron accelerator which produces about 5-10{sup 1}1 14 MeV neutrons per second by D-T reactions on a tritium-titanium fixed target. This paper concerns the tritium contamination control and monitoring aspects after some months of testing and a preliminary period of operation of the plant. The tritium monitoring system is composed of both on-line and off-line devices to control the tritium concentration in the atmosphere measured from different parts of the plant: vacuum exhaust clean up (VECU) system, stack, etc. The on-line devices are three flux monitors, that sample continuosly the air from up to eight different points in the plant. The passive sampling system is designed to select the chemical form of tritium and to collect respectively HTO and HT in two different cartridges filled with an appropriate drying material. The response of the on-line tritium monitor system are exposed and discussed: some measurements performed with atmosphere dehumidifying apparatus of this system are described and the relevant results are analysed.

Tritium contamination and monitoring at Frascati Neutron Generator

International Nuclear Information System (INIS)

Lucci, F.; Sandri, S.; Ianni, A.; Pillon, M.; Bettinali, L.

1994-11-01

The Frascati Neutron Generator (FGN) is a specialised 300 keV, 3 mA direct electrostatic deuteron accelerator which produces about 5-10 1 1 14 MeV neutrons per second by D-T reactions on a tritium-titanium fixed target. This paper concerns the tritium contamination control and monitoring aspects after some months of testing and a preliminary period of operation of the plant. The tritium monitoring system is composed of both on-line and off-line devices to control the tritium concentration in the atmosphere measured from different parts of the plant: vacuum exhaust clean up (VECU) system, stack, etc. The on-line devices are three flux monitors, that sample continuosly the air from up to eight different points in the plant. The passive sampling system is designed to select the chemical form of tritium and to collect respectively HTO and HT in two different cartridges filled with an appropriate drying material. The response of the on-line tritium monitor system are exposed and discussed: some measurements performed with atmosphere dehumidifying apparatus of this system are described and the relevant results are analysed

Target/Blanket Design for the Accelerator Production of Tritium Plant

International Nuclear Information System (INIS)

Cappiello, M. W.

1997-01-01

The Accelerator Production of Tritium Target/Blanket (T/B) system is comprised of the T/B assembly and the attendant heat removal systems. The T/B assembly produces tritium using a high energy proton beam, and a spallation neutron source. The supporting heat removal systems safely remove the heat deposited by the proton beam during both normal and off-normal conditions. All systems reside within the T/B building, which is located at the end of a linear accelerator. Protons are accelerated to an energy of 1700 MeV at a current of 100 mA and are directed onto the T/B assembly. The protons interact with tungsten and lead nuclei to produce neutrons through the process of nuclear spallation. Neutron capture in 3 He gas produces tritium which is removed on a continual basis in an adjacent Tritium Separation Facility (TSF). The T/B assembly is modular to allow for replacement of spent components and minimization of waste. Systems and components are designed with safety as a primary consideration to minimize risk to the workers and the public

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

Investigation of tritium tracer in nucleic acid components by hydrogenolysis of corresponding precursors. 7. Preparation of tritiated uracil, uridine-5'-mono-, di- and triphosphates of high molar activity

Energy Technology Data Exchange (ETDEWEB)

Myasoedov, N F; Sidorov, G V; Kuznetsova, O B; Frank-Kamenetskaya, M D; Lazurkina, T Yu; Orlova, V A

1984-01-01

Preparation of (5,6-/sup 3/H) uracil by hydrogenolysis of 5-bromo-6-chlorouracil with molar activity (1.59-1.63)x10/sup 15/ Bg/mol has been described. Hydrogenolysis reaction kinetics is studied, effect of the reaction conditions on molar activity of dehalogenation product is considered. Using enzyme fraction, separated from the E.coli cells tritium-labelled preparations of UMP, UTP and UTP from (5.6-/sup 3/H) uracil are made. Kinetics of enzymatic reactions is studied and conditions, permitting to synthesize both UMP and UTP and a mixture of nucleotides of different degree of phosphorylation in approximately equal amounts are selected. Separation of nucleotides labelled with tritium is conducted using ion exchange chromatography on DEAE cellulose. Molar activity of nucleotides labelled with tritium equals molar activity of initial (5.6-/sup 3/H) uracil, and radiochemical purity constitutes more than 95%.

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

Effects of microdistribution of tritium on dose calculations

International Nuclear Information System (INIS)

Prestwich, W.V.; Kwok, C.S.; Nunes, J.

1992-06-01

Literature and data pertaining to the microdosimetry, relative biological effectiveness, subcellular distribution, organ uptake and retention for organically-bound tritium are reviewed. The quality factor for the electron degradation spectrum associated with the radiation field of tritium β-rays in water was calculated. The value was found to be 1.9 ± .2. A related experimental measure of quality with value 1.6 ± .2 and an estimate of 1.3 based on simulation studies are cited. The average value for relative biological effectiveness for a data base of 55 values was found to be 1.8 ± .1. The influence of reference radiation, in vivo versus in vitro methodologies, and the use of tritiated thymidine or tritiated water are discussed. A methodology designed to estimate the effects of subcellular distribution is described and a suitable parameter, the localization factor defined. Estimates of this factor are made for both nuclear-bound and organically-bound tritium. Values of 4 and 1.5 respectively are suggested. Organ uptake studies in rodents following long-term feeding of organically-bound tritium are compared. The tritium is found to be unequally distributed among the tissues studied. The highest specific activity occurs in liver, with the lowest in femur. The specific activity of tritium in tissue-free water slightly exceeds that of organically-bound tritium in liver. Retention studies reveal a three-component exponential decrease of organically-bound tritium. No discernible trends of the periods of the three components with specific organs could be established. Average values of the periods are 1.2 ± .2, 10 ± 2, and 65 ± 8 days. It is concluded that specific enhancement of radiobiological effectiveness due to incorporation of tritium in DNA does probably not occur. The radiotoxicological impact of organically-bound tritium could warrant the use of a radiation weighing factor between 2 and 3

Operational experience with two tritium-effluent-monitoring systems

International Nuclear Information System (INIS)

Haynie, J.S.; Gutierrez, J.A.

1982-01-01

Two new tritium stack monitoring systems were designed and built. The operational experience of a wide-range detector with a useful range of a few μCi/m 3 to 10 8 μCi/m 3 , and a second monitoring system using an improved Kanne chamber and a new electrometer, called a Model 39 Electrometer-Chargemeter are discussed. Both tritium chambers have been designed to have a reduced sensitivity to tritium contamination, a fast response, and an integrating chargemeter with digital readout for easy conversion to microcuries. The calibration of these monitors and advantages of using these chambers over conventional systems are discussed

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.

The tritium operations experience on TFTR

International Nuclear Information System (INIS)

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

1995-01-01

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

The tritium operations experience on TFTR

International Nuclear Information System (INIS)

von Halle, A.; Gentile, C.

1994-01-01

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

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

International Nuclear Information System (INIS)

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

1986-10-01

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

Recent progress on developments of tritium safe handling techniques in Japan

International Nuclear Information System (INIS)

Watanabe, Kuniaki; Matsuyama, Masao

1993-01-01

Vast amounts of tritium will be used for thermonuclear fusion reactors. Without establishing safe handling techniques for large amounts of tritium, undoubtedly the fusion reactors will not be accepted. Japanese activity on tritium related research has considerably developed in the last 10 years. This review paper gives a brief summary of safe handling techniques developed by Japanese research groups. (author)

Tritium contamination of concrete walls and floors in tritium-handling laboratory

International Nuclear Information System (INIS)

Kawano, T.; Kuroyanagi, M.; Tabei, T.

2006-01-01

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

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

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)

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

International Nuclear Information System (INIS)

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

2013-01-01

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

Tritium release from lithium ceramics at constant temperature

International Nuclear Information System (INIS)

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

1992-02-01

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

EXOTIC: Development of ceramic tritium breeding materials

International Nuclear Information System (INIS)

Kwast, H.; Conrad, R.

1989-09-01

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

Stereo and regioselectivity in ''Activated'' tritium reactions

International Nuclear Information System (INIS)

Ehrenkaufer, R.L.E.; Hembree, W.C.; Wolf, A.P.

1988-01-01

To investigate the stereo and positional selectivity of the microwave discharge activation (MDA) method, the tritium labeling of several amino acids was undertaken. The labeling of L-valine and the diastereomeric pair L-isoleucine and L-alloisoleucine showed less than statistical labeling at the α-amino C-H position mostly with retention of configuration. Labeling predominated at the single β C-H tertiary (methyne) position. The labeling of L-valine and L-proline with and without positive charge on the α-amino group resulted in large increases in specific activity (greater than 10-fold) when positive charge was removed by labeling them as their sodium carboxylate salts. Tritium NMR of L-proline labeled both as its zwitterion and sodium salt showed also large differences in the tritium distribution within the molecule. The distribution preferences in each of the charge states are suggestive of labeling by an electrophilic like tritium species(s). 16 refs., 5 tabs

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

Tritium concentrations in flow from selected springs that discharge to the Snake River, Twin Falls-Hagerman area, Idaho

International Nuclear Information System (INIS)

Mann, L.J.

1989-01-01

Concern has been expressed that some of the approximately 30,900 curies of tritium disposed to the Snake River Plain aquifer from 1952 to 1988 at the INEL (idaho National Engineering Laboratory) have migrated to springs discharging to the Snake River in the Twin Falls-Hagerman area. To document tritium concentrations in springflow, 17 springs were sampled in November 1988 and 19 springs were sampled in March 1989. Tritium concentrations were less than the minimum detectable concentration of 0.5 pCi/mL (picocuries/mL) in November 1988 and less than the minimum detectable concentration of 0.2 pCi/mL in March 1989 the minimum detectable concentration was smaller in March 1989. The maximum contaminant level of tritium in drinking water as established by the US Environmental Protection Agency is 20 pCi/mL. US Environmental Protection Agency sample analyses indicate that the tritium concentration has decreased in the Snake River near Buhl since the 1970's. In 1974-79, tritium concentrations were less than 0.3 ± 0.2 pCi/mL in 3 of 20 samples; in 1983-88, 17 of 23 samples contaminated less than 0.3 ± 0.2 pCi/mL of tritium; the minimum detectable concentration is 0.2 pCi/mL. On the basis of decreasing tritium concentrations in the Snake River, their correlation to cessation of atmospheric weapons tests tritium concentrations in springflow less than the minimum detectable concentration, and the distribution of tritium in groundwater at the INEL, aqueous disposal of tritium at the INEL has had no measurable effect on tritium concentrations in springflow from the Snake River Plain aquifer and in the Snake River near Buhl. 15 refs., 2 figs., 3 tabs

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

Science.gov (United States)

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

2016-04-05

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

Tritium handling and vacuum considerations for the STARFIRE commercial tokamak reactor

International Nuclear Information System (INIS)

Finn, P.A.; Clemmer, R.G.; Maroni, V.A.; Dillow, C.

1979-01-01

Tritium processing and vacuum pumping requirements were analyzed for the STARFIRE commercial fusion reactor design. It was found that vacuum pumps having a helium capture probability of 0.5 (total helium pump speed 1.2 x 10 4 m 3 /s) in combination with the proposed STARFIRE limiter-vacuum concept is sufficient to achieve plasma impurity control and, simultaneously, high fractional burnup (11%). The high fractional burnup and minimum fuel recycle time result in a very low fuel cycle tritium inventory, approx. 1300 g. A Lean-T burn method that can further reduce the fuel cycle inventory by 30 to 50% is discussed. D 2 O is proposed as a first wall coolant from considerations of plasma contamination (due to hydrogen isotope permeation through coolant tubes) and enrichment of recycled tritium from the coolant circuit. Tritium recovery from solid breeders, under realistic structural and breeder materials constraints, appears to represent a formidable task. The tritium inventory in the solid breeder is estimated to be as high as 10 kg, which would make the blanket the largest single hold-up point for tritium in the plant

Transfer of tritium-labeled organic material from grass into cow's milk

International Nuclear Information System (INIS)

van den Hoek, J.; ten Have, M.H.J.; Gerber, G.B.; Kirchmann, R.

1985-01-01

Two lactating cows were given tritiated hay containing organically bound tritium (OBT) only for about 4 weeks. Tritium activity was determined in milk fat, casein, lactose, milk water, and whole milk. In one cow, milk was sampled for approximately 450 days, covering two lactation periods. At steady state, specific tritium activities in casein, lactose, and milk water were 58, 10, and 11%, respectively, of those in milk fat. Some OBT was converted into THO during catabolism and entered the body water pool. This 3 H source accounted for nearly 40% of tritium in lactose, but in casein and milk fat about 97% of tritium was derived from ingested OBT. Comparison of the specific activity of milk constituents with the specific activity of ingested hay showed the following values: 0.84 for milk fat, 0.49 for casein, 0.05 for lactose, 0.10 for milk water. Decrease of tritium activity with time could be represented by three components with different half-lives for the organic milk constituents. Those for milk fat and casein were quite similar, with a slow component of nearly 3 months

Protection against tritium radiations

International Nuclear Information System (INIS)

Bal, Georges

1964-05-01

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

ARIES-I tritium system

International Nuclear Information System (INIS)

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

1990-09-01

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

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

International Nuclear Information System (INIS)

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

2015-01-01

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

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

Energy Technology Data Exchange (ETDEWEB)

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

2015-10-15

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

The Tritium White Paper

International Nuclear Information System (INIS)

2009-01-01

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

Tritium in the Savannah River estuary and adjacent marine waters

International Nuclear Information System (INIS)

Hayes, D.W.

1979-01-01

The tritium distribution in the Savannah River estuary and adjacent marine waters was measured to provide information on the dilution, mixing and movement of Savannah River water in this region. The Savannah River marine region was chosen because the average tritium concentration in this river is approximately 5 pCi/ml, whereas other rivers in the southeastern United States of America average less than 0.5 pCi/ml. The increased tritium concentration in the Savannah River is due to releases from the Savannah River Plant of the Department of Energy. Tritium measurements have proved particularly effective in estimating the flushing time of the Savannah River estuary (2.4 days) and in delineating the relative contribution to the water masses in Ossabaw and Port Royal Sounds from the river and from sea-water. Ossabaw and Port Royal Sounds are located approximately 20 km south and north of the Savannah River estuary respectively. (author)

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

Impact limiter design for a lightweight tritium hydride vessel transport container

International Nuclear Information System (INIS)

Harding, D.C.; Longcope, D.B.; Neilsen, M.K.

1995-01-01

Sandia National Laboratories (SNL) has designed an impact-limiting system for a small, lightweight radioactive material shipping container. The Westinghouse Savannah River Company (WSRC) is developing this Type B package for the shipment of tritium, replacing the outdated LP-50 shipping container. Regulatory accident resistance requirements for Type B packages, including this new tritium package, are specified in 10 CFR 71 (NRC 1983). The regulatory requirements include a 9-meter free drop onto an unyielding target, a 1-meter drop onto a mild steel punch, and a 30-minute 800 degrees C fire test. Impact limiters are used to protect the package in the free-drop accident condition in any impact orientation without hindering the package's resistance to the thermal accident condition. The overall design of the new package is based on a modular concept using separate thermal shielding and impact mitigating components in an attempt to simplify the design, analysis, test, and certification process. Performance requirements for the tritium package's limiting system are based on preliminary estimates provided by WSRC. The current tritium hydride vessel (THV) to be transported has relatively delicate valving assemblies and should not experience acceleration levels greater than approximately 200 g's. A thermal overpack and outer stainless steel shell, to be designed by WSRC, will form the inner boundary of the impact-limiting system (see Figure 1). The mass of the package, including cargo, inner container, thermal overpack, and outer stainless steel shell (not including impact limiters) should be approximately 68 kg. Consistent with the modular design philosophy, the combined thermal overpack and containment system should be considered essentially rigid, with the impact limiters incurring all deformation

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

Science.gov (United States)

Hebert, Detlef

2011-09-01

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

Tritium inventory tracking and management

International Nuclear Information System (INIS)

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

1990-01-01

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

High-pressure tritium

International Nuclear Information System (INIS)

Coffin, D.O.

1976-01-01

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

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

International Nuclear Information System (INIS)

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

1998-01-01

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

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

International Nuclear Information System (INIS)

Waters, E.D.

1988-03-01

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

Preparations for deuterium tritium experiments on the Tokamak Fusion Test Reactor

International Nuclear Information System (INIS)

Hawryluk, R.J.; Adler, H.; Alling, P.; Ancher, C.; Anderson, H.; Anderson, J.W.; Arunasalam, V.; Ascione, G.; Ashcroft, D.; Barnes, G.

1994-04-01

The final hardware modifications for tritium operation have been completed for the Tokamak Fusion Test Reactor (TFTR). These activities include preparation of the tritium gas handling system, installation of additional neutron shielding, conversion of the toroidal field coil cooling system from water to a Fluorinet trademark system, modification of the vacuum system to handle tritium, preparation and testing of the neutral beam system for tritium operation and a final deuterium-deuterium (D-D) run to simulate expected deuterium-tritium (D-T) operation. Testing of the tritium system with low concentration tritium has successfully begun. Simulation of trace and high power D-T experiments using D-D have been performed. The physics objectives of D-T operation are production of ∼ 10 megawatts (MW) of fusion power, evaluation of confinement and heating in deuterium-tritium plasmas, evaluation of α-particle heating of electrons, and collective effects driven by alpha particles and testing of diagnostics for confined α-particles. Experimental results and theoretical modeling in support of the D-T experiments are reviewed

Preparations for deuterium--tritium experiments on the Tokamak Fusion Test Reactor*

International Nuclear Information System (INIS)

Hawryluk, R.J.; Adler, H.; Alling, P.; Ancher, C.; Anderson, H.; Anderson, J.L.; Anderson, J.W.; Arunasalam, V.; Ascione, G.; Aschroft, D.; Barnes, C.W.; Barnes, G.; Batchelor, D.B.; Bateman, G.; Batha, S.; Baylor, L.A.; Beer, M.; Bell, M.G.; Biglow, T.S.; Bitter, M.; Blanchard, W.; Bonoli, P.; Bretz, N.L.; Brunkhorst, C.; Budny, R.; Burgess, T.; Bush, H.; Bush, C.E.; Camp, R.; Caorlin, M.; Carnevale, H.; Chang, Z.; Chen, L.; Cheng, C.Z.; Chrzanowski, J.; Collazo, I.; Collins, J.; Coward, G.; Cowley, S.; Cropper, M.; Darrow, D.S.; Daugert, R.; DeLooper, J.; Duong, H.; Dudek, L.; Durst, R.; Efthimion, P.C.; Ernst, D.; Faunce, J.; Fonck, R.J.; Fredd, E.; Fredrickson, E.; Fromm, N.; Fu, G.Y.; Furth, H.P.; Garzotto, V.; Gentile, C.; Gettelfinger, G.; Gilbert, J.; Gioia, J.; Goldfinger, R.C.; Golian, T.; Gorelenkov, N.; Gouge, M.J.; Grek, B.; Grisham, L.R.; Hammett, G.; Hanson, G.R.; Heidbrink, W.; Hermann, H.W.; Hill, K.W.; Hirshman, S.; Hoffman, D.J.; Hosea, J.; Hulse, R.A.; Hsuan, H.; Jaeger, E.F.; Janos, A.; Jassby, D.L.; Jobes, F.C.; Johnson, D.W.; Johnson, L.C.; Kamperschroer, J.; Kesner, J.; Kugel, H.; Kwon, S.; Labik, G.; Lam, N.T.; LaMarche, P.H.; Laughlin, M.J.; Lawson, E.; LeBlanc, B.; Leonard, M.; Levine, J.; Levinton, F.M.; Loesser, D.; Long, D.; Machuzak, J.; Mansfield, D.E.; Marchlik, M.; Marmar, E.S.; Marsala, R.; Martin, A.; Martin, G.; Mastrocola, V.; Mazzucato, E.; McCarthy, M.P.; Majeski, R.; Mauel, M.; McCormack, B.; McCune, D.C.; McGuire, K.M.; Meade, D.M.; Medley, S.S.; Mikkelsen, D.R.; Milora, S.L.; Monticello, D.; Mueller, D.; Murakami, M.; Murphy, J.A.; Nagy, A.; Navratil, G.A.; Nazikian, R.; Newman, R.; Nishitani, T.; Norris, M.; O'Connor, T.; Oldaker, M.; Ongena, J.; Osakabe, M.; Owens, D.K.; Park, H.; Park, W.; Paul, S.F.; Pavlov, Y.I.; Pearson, G.; Perkins, F.; Perry, E.; Persing, R.; Petrov, M.; Phillips, C.K.; Pitcher, S.; Popovichev, S.; Qualls, A.L.; Raftopoulos, S.; Ramakrishnan, R.; Ramsey, A.; Rasmussen, D.A.; Redi, M.H.

1994-01-01

The final hardware modifications for tritium operation have been completed for the Tokamak Fusion Test Reactor (TFTR) [Fusion Technol. 21, 1324 (1992)]. These activities include preparation of the tritium gas handling system, installation of additional neutron shielding, conversion of the toroidal field coil cooling system from water to a Fluorinert TM system, modification of the vacuum system to handle tritium, preparation, and testing of the neutral beam system for tritium operation and a final deuterium--deuterium (D--D) run to simulate expected deuterium--tritium (D--T) operation. Testing of the tritium system with low concentration tritium has successfully begun. Simulation of trace and high power D--T experiments using D--D have been performed. The physics objectives of D--T operation are production of ∼10 MW of fusion power, evaluation of confinement, and heating in deuterium--tritium plasmas, evaluation of α-particle heating of electrons, and collective effects driven by alpha particles and testing of diagnostics for confined α particles. Experimental results and theoretical modeling in support of the D--T experiments are reviewed

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

International Nuclear Information System (INIS)

Gutowski, H.; Bracha, M.

1987-01-01

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

Tritium in plants

International Nuclear Information System (INIS)

Vichot, L.; Losset, Y.

2009-01-01