WorldWideScience

Sample records for tritium accelerator mass

  1. Use of Tritium Accelerator Mass Spectrometry for Tree Ring Analysis

    Science.gov (United States)

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

    2010-01-01

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

  2. Tritium depth profiling in carbon by accelerator mass spectrometry

    International Nuclear Information System (INIS)

    Friedrich, M.; Pilz, W.; Sun, G.; Behrisch, R.; Garcia-Rosales, C.; Bekris, N.; Penzhorn, R.-D.

    2000-01-01

    Tritium depth profiling measurements by accelerator mass spectrometry have been performed at the facility installed at the Rossendorf 3 MV Tandetron. In order to achieve a uniform erosion at the target surface inside a commercial Cs ion sputtering source and to avoid edge effects, the samples were mechanically scanned and the signals were recorded only during sputtering at the centre of the sputtered area. The sputtered negative ions were mass analysed by the injection magnet of the Tandetron. Hydrogen and deuterium profiles were measured with the Faraday cup between the injection magnet and the accelerator, while the tritium was counted after the accelerator with semiconductor detectors. Depth profiles have been measured for carbon samples which had been exposed to the plasma at the first wall of the Garching fusion experiment ASDEX-Upgrade and from the European fusion experiment JET, Culham, UK

  3. Improving tritium exposure reconstructions using accelerator mass spectrometry

    International Nuclear Information System (INIS)

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

    2004-01-01

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

  4. Improving tritium exposure reconstructions using accelerator mass spectrometry

    Science.gov (United States)

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

    2010-01-01

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

  5. 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

  6. Technology benefits resulting from accelerator production of tritium

    International Nuclear Information System (INIS)

    1998-01-01

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

  7. Tritium target manufacturing for use in accelerators

    Science.gov (United States)

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

    2001-07-01

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

  8. Accelerator Production of Tritium Programmatic Environmental Impact Statement Input Submittal

    International Nuclear Information System (INIS)

    Miller, L.A.; Greene, G.A.; Boyack, B.E.

    1996-02-01

    The Programmatic Environmental Impact Statement for Tritium Supply and Recycling considers several methods for the production of tritium. One of these methods is the Accelerator Production of Tritium. This report summarizes the design characteristics of APT including the accelerator, target/blanket, tritium extraction facility, and the balance of plant. Two spallation targets are considered: (1) a tungsten neutron-source target and (2) a lead neutron-source target. In the tungsten target concept, the neutrons are captured by the circulating He-3, thus producing tritium; in the lead target concept, the tritium is produced by neutron capture by Li-6 in a surrounding lithium-aluminum blanket. This report also provides information to support the PEIS including construction and operational resource needs, waste generation, and potential routine and accidental releases of radioactive material. The focus of the report is on the impacts of a facility that will produce 3/8th of the baseline goal of tritium. However, some information is provided on the impacts of APT facilities that would produce smaller quantities

  9. 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

  10. Linear accelerator for production of tritium: Physics design challenges

    Energy Technology Data Exchange (ETDEWEB)

    Wangler, T.P.; Lawrence, G.P.; Bhatia, T.S.; Billen, J.H.; Chan, K.C.D.; Garnett, R.W.; Guy, F.W.; Liska, D.; Nath, S.; Neuschaefer, G.; Shubaly, M.

    1990-01-01

    In the summer of 1989, a collaboration between Los Alamos National Laboratory and Brookhaven National Laboratory conducted a study to establish a reference design of a facility for accelerator production of tritium (APT). The APT concept is that of a neutron-spallation source, which is based on the use of high-energy protons to bombard lead nuclei, resulting in the production of large quantities of neutrons. Neutrons from the lead are captured by lithium to produce tritium. This paper describes the design of a 1.6-GeV, 250-mA proton cw linear accelerator for APT.

  11. Tritium depth profiling in carbon samples from fusion experiments

    International Nuclear Information System (INIS)

    Friedrich, M.; Pilz, W.; Sun, G.; Behrisch, R.; Garcia-Rosales, C.; Bekris, N.; Penzhorn, R.-D.

    2000-01-01

    Tritium depth profiling by accelerator mass spectrometry has been performed at the Rossendorf 3 MV Tandetron. Tritium particles are counted after the accelerator using a semiconductor detector, while deuterium and other light elements are simultaneously measured with the Faraday cup between the injection magnet and the accelerator. Depth profiles have been measured in carbon samples cut from the first wall tiles of the Garching fusion experiment ASDEX-Upgrade and of the European fusion experiment JET, Culham/UK. Tritium contents in the JET samples were up to six orders higher than in samples from ASDEX-Upgrade. Tritium beam currents from samples with high tritium content were measured partly in the Faraday cup before the accelerator. A dedicated tritium AMS facility with an air-insulated 100 kV tandem accelerator is under construction

  12. Medical Isotope Production With The Accelerator Production of Tritium (APT) Facility

    International Nuclear Information System (INIS)

    Buckner, M.; Cappiello, M.; Pitcher, E.; O'Brien, H.

    1998-01-01

    In order to meet US tritium needs to maintain the nuclear weapons deterrent, the Department of Energy (DOE) is pursuing a dual track program to provide a new tritium source. A record of decision is planned for late in 1998 to select either the Accelerator Production of Tritium (APT) or the Commercial Light Water Reactor (CLWR) as the technology for new tritium production in the next century. To support this decision, an APT Project was undertaken to develop an accelerator design capable of producing 3 kg of tritium per year by 2007 (START I requirements). The Los Alamos National Laboratory (LANL) was selected to lead this effort with Burns and Roe Enterprises, Inc. (BREI) / General Atomics (GA) as the prime contractor for design, construction, and commissioning of the facility. If chosen in the downselect, the facility will be built at the Savannah River Site (SRS) and operated by the SRS Maintenance and Operations (M ampersand O) contractor, the Westinghouse Savannah River Company (WSRC), with long-term technology support from LANL. These three organizations (LANL, BREI/GA, and WSRC) are working together under the direction of the APT National Project Office which reports directly to the DOE Office of Accelerator Production which has program authority and responsibility for the APT Project

  13. Accelerator production of tritium plant design and supporting engineering development and demonstration work

    International Nuclear Information System (INIS)

    Lisowski, P.W.

    1997-11-01

    Tritium is an isotope of hydrogen with a half life of 12.3 years. Because it is essential for US thermonuclear weapons to function, tritium must be periodically replenished. Since K reactor at Savannah River Site stopped operating in 1988, tritium has been recycled from dismantled nuclear weapons. This process is possible only as long as many weapons are being retired. Maintaining the stockpile at the level called for in the present Strategic Arms Reduction Treaty (START-I) will require the Department of Energy to have an operational tritium production capability in the 2005--2007 time frame. To make the required amount of tritium using an accelerator based system (APT), neutrons will be produced through high energy proton reactions with tungsten and lead. Those neutrons will be moderated and captured in 3 He to make tritium. The APT plant design will use a 1,700 MeV linear accelerator operated at 100 mA. In preparation for engineering design, starting in October 1997 and subsequent construction, a program of engineering development and demonstration is underway. That work includes assembly and testing of the first 20 MeV of the low energy plant linac at 100 mA, high-energy linac accelerating structure prototyping, radiofrequency power system improvements, neutronic efficiency measurements, and materials qualifications

  14. 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].

  15. Investigation of aluminised steel as a barrier to tritium using accelerator-based and hydrogen permeation techniques

    Energy Technology Data Exchange (ETDEWEB)

    Sokhi, R S; Forcey, K S; Ross, D K; Earwaker, L G [Birmingham Univ. (UK). School of Physics and Space Research

    1989-04-01

    Aluminised steel has been proposed as a barrier to tritium permeation in fusion reactors. The properties of these materials as tritium barriers have been studied using accelerator-based techniques and hydrogen permeation methods. The aluminide layers has been characterised by Rutherford backscattering spectroscopy (RBS) and nuclear reaction analysis (NRA) techniques using the 3 MV Dynamitron accelerator based at the School of Physics and Space Research Radiation Centre. The effectiveness of the aluminide layer as a tritium barrier has been measured directly by a conventional permeation apparatus over a range of temperatures. The effect of high temperatures on the structure of the aluminide layer has been examined. Any correlation between the composition of the layer and its effectiveness as a tritium barrier is also discussed. (orig.).

  16. Safety management of a high energy accelerator used in the production of tritium

    International Nuclear Information System (INIS)

    Stark, R.M.; Brown, N.W.; Allen C.L.

    1997-01-01

    Interest in a high energy accelerator for producing tritium raises considerations regarding facility Safety Management. Accelerator facility hazards require safety analysis to consider factors such as: safe management of a large flux of very high energy neutrons, sustained operation in a very high energy proton and neutron field, neutron irradiation of a variety of materials, and handling and processing of significant quantities of tritium. Safety considerations of support systems and potential effects of magnetic fields must also be included. Existing Safety Management techniques, safety standards, and criteria for operation of high energy accelerators provide considerable guidance. These must, however, be reviewed to determine their appropriate use for safe operation of a very large, tritium-producing accelerator. New or revised safety standards may be required to establish and maintain the safe operating-envelope. The goal will be to develop a set of tailored standards and criteria that provide a reasonable operational envelope and assure adequate public, worker, and environmental safety. The generation of an appropriate set of safety standards and criteria will include several activities. One activity will involve evaluation of proposed facility designs to determine possible hazards. Another activity will involve a detailed review of existing accelerator safety management systems. A third activity will involve the review of operating histories of existing facilities. Facilities approximating the characteristics of the anticipated tritium production facility will be considered. Following completion of these activities a proposed Safety Management System and criteria for application to these facilities will be drafted. The need for new analytical methods and for additional safety standards will be identified. The draft document will then be reviewed and revised to establish the standards and criteria within the appropriate Department of Energy framework

  17. Progress report on the accelerator production of tritium materials irradiation program

    International Nuclear Information System (INIS)

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

    1997-01-01

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

  18. 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.

  19. 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

  20. Tritium depth profiling by AMS in carbon samples from fusion experiments

    International Nuclear Information System (INIS)

    Friedrich, M.; Pilz, W.; Sun, G.; Behrisch, R.; Garcia-Rosales, C.

    2001-01-01

    Tritium depth profiling measurements by accelerator mass spectrometry have been performed at a facility installed at the Rossendorf 3 MV Tandetron. In order to achieve an uniform erosion at the target surface inside of a commercial Cs ion sputtering source and to avoid edge effects, the samples were mechanically scanned inside of a commercial Cs sputter ion source. The sputtered negative ions were mass analysed by the injection magnet of the Tandetron. The tritium ions are counted after the acceleration with semiconductor detectors. Depth profiles have been measured for carbon samples which had been exposed to the plasma at the first wall of the Garching fusion experiment ASDEX-Upgrade and from the European fusion experiment JET, Culham/UK. A dedicated AMS facility with an air-insulated 100 kV tandem accelerator for depth profiling measurements at samples with high tritium concentration is under construction. First results of test operation are presented. (orig.)

  1. New applications of accelerator mass spectrometry

    International Nuclear Information System (INIS)

    Davis, J.C.

    1991-01-01

    Since its invention in the late 70's, and reduction to near-routine practice by the mid-80's, accelerator mass spectrometry (AMS) has become a powerful tool for archaeological and geochemical measurements in which cosmogenic isotopes such as 10 Be, 14 C, 26 Al, 36 Cl and 129 I are used as either tracers or chronometers. The utility of such measurements is demonstrated by the fact that most accelerators having AMS capabilities have significant backlogs of samples awaiting measurement. In designing and justifying a new accelerator facility in which AMS was to be a major feature, we sought to advance the field and increase the resources available for it by two steps: (1) development of new research applications in which intentionally added isotopic labels were used rather than just naturally present ones; and (2) enhancement of spectrometer throughout, making new classes of experiments possible by greatly increasing the number of samples that could be measured in individual experiments. Results of the effort to date suggest that development of a family of very small spectrometers optimized for just tritium and/or radiocarbon will be attractive in the near future

  2. The time series variations of tritium concentration in precipitation and its relationships to the rainfall-inducing air mass

    International Nuclear Information System (INIS)

    Shimada, Jun

    1978-01-01

    The author measured the tritium concentration in precipitation of Tokyo for every ten-day period from August 1972 to May 1974. Judging from the daily synoptic weather chart, the rainfall-inducing air masses in Japan were classified into five types; polar maritime air mass (Pm), polar continental air mass (Pc), tropical maritime air mass (Tm), tropical continental air mass (Tc), and equatorial maritime air mass (Em). And the precipitation for every ten-day period sampled for tritium measurement were classified into these five types. Based on this classification, it is confirmed that there exist clear difference in the tritium concentration between the rainfall from the continental air mass and ones from the maritime air mass. It is characteristic that the tritium concentration in rainfall induced by equatorial maritime air mass such as typhoon in summer and early fall season is very low whereas the tritium concentration in rainfall and snowfall induced directly by the polar continental air mass in late winter season is very high. The regional difference of the tritium concentration in intermonthly precipitation could considerably be explained by this synoptic meteological classification of rainfall-inducing air mass. In spite of these regional difference of tritium concentration in precipitation, use of the tritium concentration of Tokyo as a representative value of Japan may be allowed because of the similarities of the changing pattern and annual mean tritium concentration. The time series variations of tritium concentration in precipitation of Tokyo from August 1972 to December 1977, Tsukuba from December 1976 to April 1978, and Nagaoka from April 1977 to March 1978 are listed. (author)

  3. Development of a low tritium partial pressure permeation system for mass transport measurement in lead lithium eutectic

    International Nuclear Information System (INIS)

    Pawelko, R.; Shimada, M.; Katayama, K.; Fukada, S.; Terai, T.

    2014-01-01

    A new experimental system designed to investigate tritium mass transfer properties in materials important to fusion technology is operational at the Safety and Tritium Applied Research (STAR) facility located at the Idaho National Laboratory (INL). The tritium permeation measurement system was developed as part of the Japan/US TITAN collaboration to investigate tritium mass transfer properties in liquid lead lithium eutectic (LLE) alloy. The system is similar to a hydrogen/deuterium permeation measurement system developed at Kyushu University and also incorporates lessons learned from previous tritium permeation experiments conducted at the STAR facility. This paper describes the experimental system that is configured specifically to measure tritium mass transfer properties at low tritium partial pressures. We present preliminary tritium permeation results for α-Fe and α-Fe/LLE samples at 600degC and at tritium partial pressures between 1.0E-3 and 2.4 Pain helium. The preliminary results are compared with literature data. (author)

  4. 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

  5. An assessment of anti-neutrino mass determination via electrostatic measurements of tritium beta-decay

    International Nuclear Information System (INIS)

    Le Bas, P.A.

    1984-01-01

    Data on the mass of the anti-neutrino determined via electrostatic measurements of tritium beta-decay are assessed. Relativistic calculations concerning the finite mass of the electron anti-neutrino and the recoil of the nucleus, are given for the theoretical end-point spectrum of tritium beta-decay. The specifications are given for an electrostatic Spherical Retarding Beta-Spectrometer, and an electrostatic Cylindrical Mirror Analyser, both used in the tritium beta-decay experiment. The electrostatic measurements lead to a value of less than 50 ev (90% C.L.) for the electron anti-neutrino mass. These results are discussed in terms of the resolution of the electrostatic equipment and the Monte Carlo simulations of the data collection. (UK)

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

    International Nuclear Information System (INIS)

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

    2001-01-01

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

  7. Molecular effects in the neutrino mass determination from beta-decay of the tritium molecule

    International Nuclear Information System (INIS)

    Fackler, O.; Jeziorski, B.; Kolos, W.; Szalewicz, K.; Monkhorst, H.J.; Mugge, M.

    1986-03-01

    Molecular final state energies and transition probabilities have been computed for beta-decay of the tritium molecule. The results are of sufficient accuracy to make a determination of the electron neutrino rest mass with an error not exceeding a few tenths of an electron volt. Effects of approximate models of tritium beta-decay on the neutrino mass determination are discussed. 14 refs., 3 figs., 1 tab

  8. Scientific and engineering services for the LANCE/ER accelerator production of tritium (APT) project

    International Nuclear Information System (INIS)

    1994-01-01

    The APT project office is conducting a preconceptual design study for an accelerator driven concept to produce tritium. The facility will require new technology in many areas, since the scale of this accelerator is significantly larger then any in operation to date. The facility is composed of four subsystems: accelerator, target ampersand blanket, balance of plant, and tritium purification system (TPS). New physics realms will be entered in order for the concept to be feasible; for example, extremely high energy levels of the entering protons that induce (multiplicative) spallation of the neutrons from the high Z target will occur. These are complex and require advance codes (MCNP) to predict the physics interactions and as well as deleterious material effects in the surrounding structures. Other issues include component cooling and complex thermal-hydraulics effects within the blanket and the beam open-quotes window.close quotes In order to support a DOE mandated fast ROD schedule, Los Alamos APT staff will be provided with senior, engineering technical support staff with direct APT technology experience and whom are open-quotes on siteclose quotes. This report contains resumes of the staff

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

    International Nuclear Information System (INIS)

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

    1986-01-01

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

  10. 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

  11. RAMI modeling of selected balance of plant systems for the proposed Accelerator Production of Tritium (APT) project

    International Nuclear Information System (INIS)

    Radder, J.A.; Cramer, D.S.

    1997-01-01

    In order to meet Department of Energy (DOE) Defense Program requirements for tritium in the 2005-2007 time frame, new production capability must be made available. The Accelerator Production of Tritium (APT) Plant is being considered as an alternative to nuclear reactor production of tritium, which has been the preferred method in the past. The proposed APT plant will use a high-power proton accelerator to generate thermal neutrons that will be captured in 3 He to produce tritium (3H). It is expected that the APT Plant will be built and operated at the DOE's Savannah River Site (SRS) in Aiken, South Carolina. Discussion is focused on Reliability, Availability, Maintainability, and Inspectability (RAMI) modeling of recent conceptual designs for balance of plant (BOP) systems in the proposed APT Plant. In the conceptual designs for balance of plant (BOP) systems in the proposed APT Plant. In the conceptual design phase, system RAMI estimates are necessary to identify the best possible system alternative and to provide a valid picture of the cost effectiveness of the proposed system for comparison with other system alternatives. RAMI estimates in the phase must necessarily be based on generic data. The objective of the RAMI analyses at the conceptual design stage is to assist the designers in achieving an optimum design which balances the reliability and maintainability requirements among the subsystems and components

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

    International Nuclear Information System (INIS)

    Takata, Hiroki; Nishikawa, Masabumi; Kamimae, Kozo

    2005-01-01

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

  13. Accelerator-based ultrasensitive mass spectrometry

    International Nuclear Information System (INIS)

    Gove, H.E.

    1985-01-01

    This chapter describes a new mass spectrometry technique involving charged particle accelerators normally used for basic research in nuclear science. Topics considered include the limitations of conventional mass spectrometry, the limitations of the direct measurement of radioactive decay, mass spectrometry using a tandem electrostatic accelerator, mass spectrometry using a cyclotron, how accelerator mass spectrometry circumvents the limitations of conventional mass spectrometry, measurements of stable isotopes, nuclear physics and astrophysics applications, modifications to existing accelerators, descriptions of dedicated systems, and future applications

  14. 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

  15. Relevance of d-D interactions on neutron and tritium production in IFMIF-EVEDA accelerator prototype

    International Nuclear Information System (INIS)

    Mayoral, A.; Sanz, J.; Sauvan, P.; Lopez, D.; Garcia, M.; Ogando, F.

    2011-01-01

    In the IFMIF-EVEDA accelerator prototype, deuterium is implanted in the components due to beam losses and in the beam dump, where the beam is stopped. The interaction of the deuterons with the deuterium previously implanted leads to the production of neutrons and tritium, which are important issues for radioprotection and safety analysis. A methodology to assess these production pathways in more realistic approach has been developed. The new tools and their main achievement are: (i) an 'effective diffusivity coefficient' (deduced from available experimental data) that enables simulation of the diffusion phase, and (ii) the MCUNED code (able to handle deuteron transport libraries) allows to simulate the transport-slowdown of deuteron/tritium (to get the concentration profiles) and the neutron/tritium productions from d-Cu and d-D for up to 9 MeV incident deuteron. The results with/without theses tools are presented and their effect on the relevance of d-D sources versus d-Cu is evaluated.

  16. Optimization of mass of plastic scintillator film for flow-cell based tritium monitoring: a Monte Carlo study

    International Nuclear Information System (INIS)

    Roy, Arup Singha; Palani Selvam, T.; Raman, Anand; Raja, V.; Chaudhury, Probal

    2014-01-01

    Over the years, various types of tritium-in-air monitors have been designed and developed based on different principles. Ionization chamber, proportional counter and scintillation detector systems are few among them. A plastic scintillator based, flow-cell type online tritium-in-air monitoring system was developed for online monitoring of tritium in air. The value of the scintillator mass inside the cell-volume, which maximizes the response of the detector system, should be obtained to get maximum efficiency. The present study is aimed to optimize the amount of mass of the plastic scintillator film for the flow-cell based tritium monitoring instrument so that maximum efficiency is achieved. The Monte Carlo based EGSnrc code system has been used for this purpose

  17. 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

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

    International Nuclear Information System (INIS)

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

    1985-01-01

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

  19. Determination of the neutrino mass from the beta decay of gaseous molecular tritium

    International Nuclear Information System (INIS)

    Decman, D.J.; Stoeffl, W.

    1992-06-01

    We set an upper limit of 8 eV for the mass of the electron antineutrino from studying the beta decay of tritium. We use a gaseous molecular tritium source, a high resolution magnetic spectrometer and a low background counting system to minimize the systematic errors encountered in these measurements. Our calibration data with radioactive 83m Kr enables us to measure our system response function and a good deal of atomic physics data. In addition to our end point results we have made the first measurement of the tritium beta decay spectrum below 200 keV. We find an excess of very low energy electrons which arise from molecular processes of the 3 He-T + ion

  20. Robotics development for the accelerator production of tritium

    International Nuclear Information System (INIS)

    Ward, C.R.

    2000-01-01

    The Accelerator Production of Tritium (APT) has been proposed as the source of tritium for the United States in the next century. The APT will accelerate protons that will strike replaceable tungsten target modules. The tungsten target modules generate neutrons that interact with blanket modules and other modules where 3 He gas is turned into tritium. The target and blanket modules are predicted to require replacement every one to ten years, depending on their location. The target modules may weigh as much as 85 tons (77 metric tons) each. All of the modules will be contained in a target/blanket vessel, which is in a shielded facility. The spent modules will be radioactive, so that remote replacement of the modules will be required. The modules will be 27 feet (8.23 m) high and the top of the modules, where most of the remote operations will occur, will be approximately 20 feet (6.1 m) down into the target/blanket vessel. The immense weights of the modules, the long reaches required and the requirement for completely remote operation of at least part of the operation, make this a unique and challenging task. Initially, manual fastening and unfastening of the jumper flanges on the modules as well as manual valve operation was proposed followed by remote replacement of the modules. This manual/remote operation was demonstrated with a computer-generated, dynamic, 3-D simulation. After review of the simulation, this operation was changed to be a complete remote operation. Complete remote operation brought about the concept of a remotely operated bridge crane and a remotely operated, bridge-mounted, manipulator to perform the entire replacement operation. A second simulation showed the intended operation of the remote concept and was instrumental in developing the requirements for the equipment and end effectors for this concept. The concept included development of end effectors for the following tasks: flange nut fastening and unfastening, flange lifting and latch

  1. Direct search for neutrino mass and anomaly in the tritium beta-spectrum: Status of 'Troitsk neutrino mass' experiment

    International Nuclear Information System (INIS)

    Lobashev, V.M.; Aseev, V.N.; Belesev, A.I.; Berlev, A.I.; Geraskin, E.V.; Golubev, A.A.; Kazachenko, O.V.; Kuznetsov, Yu.E.; Ostroumov, R.P.; Rivkis, L.A.; Stern, B.E.; Titov, N.A.; Zadoroghny, C.V.; Zakharov, Yu.I.

    2000-01-01

    Results of the 'Troitsk ν-mass' experiment on search for the neutrino rest mass in the tritium beta-decay are presented. New data on the time dependence of the anomalous, bump-like structure at the end of the beta spectrum reported earlier are discussed. Possible systematics is considered in view of contradiction of 'Troitsk nu-mass' observation with those of 'Mainz neutrino' set-up. An upper limit for electron antineutrino rest mass remains at m ν 2 at 95% C.L

  2. Direct search for neutrino mass and anomaly in the tritium beta-spectrum

    International Nuclear Information System (INIS)

    Lobashev, V.M.; Assev, V.N.; Belesev, A.I.; Berlev, A.I.; Geraskin, E.V.; Golubev, A.A.; Kazachenko, O.V.; Kuznetsov, Y.E.; Ostroumov, R.P.; Rivkis, L.A.; Stern, B.E.; Titov, N.A.; Zasoroghny, C.V.; Zakharov, Y.I.

    2001-01-01

    Results of the ''Troitsk ν-mass'' experiment on search for the neutrino rest mass in the tritium beta-decay are presented. Study of time dependence of anomalous, bump-like structure at the end of the beta spectrum reported earlier gives indication of a periodic shift of the position of the bump with respect to the end-point energy with period of 0.5 year. New upper limit for electron antineutrino rest mass m ν 2 is derived after accounting for the bump. (authors)

  3. Tritium analysis at TFTR

    International Nuclear Information System (INIS)

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

    1995-01-01

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

  4. An overview of tritium production

    International Nuclear Information System (INIS)

    He Kaihui; Huang Jinghua; Feng Kaiming

    2002-01-01

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

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

    International Nuclear Information System (INIS)

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

    1991-04-01

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

  6. 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

  7. 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.

  8. Tritium containing polymers having a polymer backbone substantially void of tritium

    Science.gov (United States)

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

    1992-03-31

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

  9. Mass spectrometry with accelerators.

    Science.gov (United States)

    Litherland, A E; Zhao, X-L; Kieser, W E

    2011-01-01

    As one in a series of articles on Canadian contributions to mass spectrometry, this review begins with an outline of the history of accelerator mass spectrometry (AMS), noting roles played by researchers at three Canadian AMS laboratories. After a description of the unique features of AMS, three examples, (14)C, (10)Be, and (129)I are given to illustrate the methods. The capabilities of mass spectrometry have been extended by the addition of atomic isobar selection, molecular isobar attenuation, further ion acceleration, followed by ion detection and ion identification at essentially zero dark current or ion flux. This has been accomplished by exploiting the techniques and accelerators of atomic and nuclear physics. In 1939, the first principles of AMS were established using a cyclotron. In 1977 the selection of isobars in the ion source was established when it was shown that the (14)N(-) ion was very unstable, or extremely difficult to create, making a tandem electrostatic accelerator highly suitable for assisting the mass spectrometric measurement of the rare long-lived radioactive isotope (14)C in the environment. This observation, together with the large attenuation of the molecular isobars (13)CH(-) and (12)CH 2(-) during tandem acceleration and the observed very low background contamination from the ion source, was found to facilitate the mass spectrometry of (14)C to at least a level of (14)C/C ~ 6 × 10(-16), the equivalent of a radiocarbon age of 60,000 years. Tandem Accelerator Mass Spectrometry, or AMS, has now made possible the accurate radiocarbon dating of milligram-sized carbon samples by ion counting as well as dating and tracing with many other long-lived radioactive isotopes such as (10)Be, (26)Al, (36)Cl, and (129)I. The difficulty of obtaining large anion currents with low electron affinities and the difficulties of isobar separation, especially for the heavier mass ions, has prompted the use of molecular anions and the search for alternative

  10. Analysis of air mass trajectories to explain observed variability of tritium in precipitation at the Southern Sierra Critical Zone Observatory, California, USA.

    Science.gov (United States)

    Visser, Ate; Thaw, Melissa; Esser, Brad

    2018-01-01

    Understanding the behavior of tritium, a radioactive isotope of hydrogen, in the environment is important to evaluate the exposure risk of anthropogenic releases, and for its application as a tracer in hydrology and oceanography. To understand and predict the variability of tritium in precipitation, HYSPLIT air mass trajectories were analyzed for 16 aggregate precipitation samples collected over a 2 year period at irregular intervals at a research site located at 2000 m elevation in the southern Sierra Nevada (California, USA). Attributing the variation in tritium to specific source areas confirms the hypothesis that higher latitude or inland sources bring higher tritium levels in precipitation than precipitation originating in the lower latitude Pacific Ocean. In this case, the source of precipitation accounts for 79% of the variation observed in tritium concentrations. Air mass trajectory analysis is a promising tool to improve the predictions of tritium in precipitation at unmonitored locations and thoroughly understand the processes controlling transport of tritium in the environment. Copyright © 2017 Elsevier Ltd. All rights reserved.

  11. 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).

  12. 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).

  13. Desorption of tritium and helium from high dose neutron irradiated beryllium

    Science.gov (United States)

    Kupriyanov, I. B.; Nikolaev, G. N.; Vlasov, V. V.; Kovalev, A. M.; Chakin, V. P.

    2007-08-01

    The effect of high dose neutron irradiation on tritium and helium desorption in beryllium is described. Beryllium samples were irradiated in the SM and BOR-60 reactors to a neutron fluences ( E > 0.1 MeV) of (5-16) × 10 22 cm -2 at 70-100 °C and 380-420 °C. A mass-spectrometry technique was used in out of pile tritium release experiments during stepped annealing in the 250-1300 °C temperature range. The total amount of helium accumulated in irradiated beryllium samples varied from 6000 to 7200 appm. The first signs of tritium and helium release were detected at temperature of 312-445 °C and 500-740 °C, respectively. It is shown that most tritium (˜82%) from sample irradiated at 70-100 °C releases in temperature range of 312-700 °C before the beginning of helium release (740 °C). In the case of beryllium sample irradiated at 380-420 °C, tritium release starts at a higher temperature ( Ts > Tann = 445 °C) and most of the tritium (˜99.8%) is released concurrently with helium which could be considered as evidence of co-existence of partial amounts of tritium and helium in common bubbles. Both the Be samples differ little in the upper temperatures of gas release: 745 and 775 °C for tritium; 1140 and 1160 °C for helium. Swelling of beryllium starts to play a key role in accelerating tritium release at Tann > 600 °C and in helium release - at Tann > 750 °C.

  14. Laboratory of acceleration mass spectrometry

    International Nuclear Information System (INIS)

    Hybler, P.; Chrapan, J.

    2002-01-01

    In this paper authors describe the principle of the method of acceleration mass spectrometry and the construction plans of this instrument at the Faculty of ecology and environmental sciences in Banska Stiavnica. Using of this instrument for radiocarbon dating is discussed. A review of laboratories with acceleration mass spectrometry is presented

  15. Preliminary Disposal Analysis for Selected Accelerator Production of Tritium Waste Streams

    International Nuclear Information System (INIS)

    Ades, M.J.; England, J.L.

    1998-06-01

    A preliminary analysis was performed for two selected Accelerator Production of Tritium (APT) generated mixed and low-level waste streams to determine if one mixed low-level waste (MLLW) stream that includes the Mixed Waste Lead (MWL) can be disposed of at the Nevada Test Site (NTS) and at the Hanford Site and if one low-level radioactive waste (LLW) stream, that includes the Tungsten waste stream (TWS) generated by the Tungsten Neutron Source modules and used in the Target/Blanket cavity vessel, can be disposed of in the LLW Vaults at the Savannah River Plant (SRP). The preliminary disposal analysis that the radionuclide concentrations of the two selected APT waste streams are not in full compliance with the Waste Acceptance Criteria (WAC) and the Performance Assessment (PA) radionuclide limits of the disposal sites considered

  16. 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

  17. Symposium on accelerator mass spectrometry

    Energy Technology Data Exchange (ETDEWEB)

    None

    1981-01-01

    The area of accelerator mass spectrometry has expanded considerably over the past few years and established itself as an independent and interdisciplinary research field. Three years have passed since the first meeting was held at Rochester. A Symposium on Accelerator Mass Spectrometry was held at Argonne on May 11-13, 1981. In attendance were 96 scientists of whom 26 were from outside the United States. The present proceedings document the program and excitement of the field. Papers are arranged according to the original program. A few papers not presented at the meeting have been added to complete the information on the status of accelerator mass spectrometry. Individual papers were prepared separately for the data base.

  18. Symposium on accelerator mass spectrometry

    International Nuclear Information System (INIS)

    1981-01-01

    The area of accelerator mass spectrometry has expanded considerably over the past few years and established itself as an independent and interdisciplinary research field. Three years have passed since the first meeting was held at Rochester. A Symposium on Accelerator Mass Spectrometry was held at Argonne on May 11-13, 1981. In attendance were 96 scientists of whom 26 were from outside the United States. The present proceedings document the program and excitement of the field. Papers are arranged according to the original program. A few papers not presented at the meeting have been added to complete the information on the status of accelerator mass spectrometry. Individual papers were prepared separately for the data base

  19. Exposure Control for Operations and Maintenance at the Accelerator Production of Tritium

    International Nuclear Information System (INIS)

    McGuire, D.H.

    1998-09-01

    The APT will be designed and operated to support continuous tritium production. Tritium is an essential ingredient in U.S. nuclear weapons. The APT will be designed and staffed to support continuous production of tritium by trained, qualified, and certified personnel

  20. Flow distribution in the accelerator-production-of-tritium target

    International Nuclear Information System (INIS)

    Siebe, D.A.; Spatz, T.L.; Pasamehmetoglu, K.O.; Sherman, M.P.

    1999-01-01

    Achieving nearly uniform flow distributions in the accelerator production of tritium (APT) target structures is an important design objective. Manifold effects tend to cause a nonuniform distribution in flow systems of this type, although nearly even distribution can be achieved. A program of hydraulic experiments is underway to provide a database for validation of calculational methodologies that may be used for analyzing this problem and to evaluate the approach with the most promise for achieving a nearly even flow distribution. Data from the initial three tests are compared to predictions made using four calculational methods. The data show that optimizing the ratio of the supply-to-return-manifold areas can produce an almost even flow distribution in the APT ladder assemblies. The calculations compare well with the data for ratios of the supply-to-return-manifold areas spanning the optimum value. Thus, the results to date show that a nearly uniform flow distribution can be achieved by carefully sizing the supply and return manifolds and that the calculational methods available are adequate for predicting the distributions through a range of conditions

  1. RF system considerations for accelerator production of tritium and the transmutation of nuclear waste

    International Nuclear Information System (INIS)

    Tallerico, P.J.; Lynch, M.T.

    1993-01-01

    RF driven proton accelerators for the transmutation of nuclear waste (ATW) or for the production of tritium (APT) require unprecedented amounts of CW RF power at UHF frequencies. For both systems, the baseline design is for 246 MW at 700 MHz and 8,5 MW at 350 MHz. The main technical challenges are how to design and build such a large system so that it has excellent reliability, high efficiency, and reasonable capital cost. The issues associated with the selection of the RF amplifier and the sizes of the power supplies are emphasized in this paper

  2. Photoproduction of tritium

    International Nuclear Information System (INIS)

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

    1995-01-01

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

  3. 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

  4. Reconstructing Tritium Exposure Using Tree Rings at Lawrence Berkeley National Laboratory, California

    Science.gov (United States)

    LOVE, ADAM H.; HUNT, JAMES R.; KNEZOVICH, JOHN P.

    2010-01-01

    Annual tritium exposures were reconstructed using tree cores from Pinus jeffreyi and Eucalyptus globulus near a tritiated water vapor release stack. Both tritium (3H) and carbon-14 (14C) from the wood were measured from milligram samples using accelerator mass spectrometry. Because the annual nature of the eucalyptus tree rings was in doubt, 14C measurements provided growth rates used to estimate the age for 3H determinations. A 30-yr comparison of organically bound tritium (OBT) levels to reported 3H release data is achieved using OBT measurements from three trees near the stack. The annual average 3H, determined from atmospheric water vapor monitoring stations, is comparable to the OBT in proximal trees. For situations without adequate historical monitoring data, this measurement-based historical assessment provides the only independent means of assessing exposure as compared to fate and transport models that require prior knowledge of environmental conditions and 3H discharge patterns. PMID:14572081

  5. Implantation measurements to determine tritium permeation in first wall structures

    International Nuclear Information System (INIS)

    Holland, D.F.; Causey, R.A.

    1983-01-01

    A principal safety concern for a D-T burning fusion reactor is release of tritium during routine operation. Tritium implantation into first wall structures, and subsequent permeation into coolants, is potentially an important source of tritium loss. This paper reports on an experiment in which an ion accelerator was used to implant deuterium atoms in a stainless steel disk to simulate tritium implantation in first wall structures. The permeation rate was measured under various operating conditions. These results were used in the TMAP computer code to determine potential tritium loss rates for fusion reactors

  6. Implantation measurements to determine tritium permeation in first-wall structures

    International Nuclear Information System (INIS)

    Holland, D.F.; Causey, R.A.; Sattler, M.L.

    1983-01-01

    A principal safety concern for a D-T burning fusion reactor is release of tritium during routine operation. Tritium implantation into first-wall structures, and subsequent permeation into coolants, is potentially an important source of tritium loss. This paper reports on an experiment in which an ion accelerator was used to implant deuterium atoms in a stainless steel disk to simulate tritium implantation in first-wall structures. The permeation rate was measured under various operating conditions. These results were used in the TMAP computer code to determine potential tritium loss rates for fusion reactors

  7. Accelerator production of tritium authorization basis strategy

    International Nuclear Information System (INIS)

    Miller, L.A.; Edwards, J.; Rose, S.

    1996-01-01

    The Accelerator Production of Tritium (APT) project has proposed a strategy to develop the APT authorization basis and safety case based on DOE orders and fundamental requirements for safe operation. The strategy is viable regardless of whether the APT is regulated by DOE or by an external regulatory body. Currently the operation of Department of Energy (DOE) facilities is authorized by DOE and regulated by DOE orders and regulations while meeting the environmental protection requirements of the Environmental Protection Agency (EPA) and the states. In the spring of 1994, Congress proposed legislation and held hearings related to requiring all DOE operations to be subject to external regulation. On January 25, 1995, DOE, with the support of the White House Council on Environmental Quality, created the Advisory Committee on External Regulation of Department of Energy Nuclear Safety. This committee divided its recommendations into three areas: (1) facility safety, (2) worker safety, and (3) environmental protection. In the area of facility safety the committee recommended external regulation of DOE nuclear facilities by either the Nuclear Regulatory Commission (NRC) or a restructured Defense Nuclear Facilities Safety Board (DNFSB). In the area of worker safety, the committee recommended that the Occupational Safety and Health Administration (OSHA) regulate DOE nuclear facilities. In the environmental protection area, the committee did not recommend a change in the regulation by the EPA and the states of DOE nuclear facilities. If these recommendations are accepted, all DOE nuclear facilities will be impacted to some extent

  8. PRODUCTION OF TRITIUM

    Science.gov (United States)

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

    1963-02-26

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

  9. A small and compact AMS facility for tritium depth profiling

    Indian Academy of Sciences (India)

    employing diamond-like carbon (DLC) stripper foils at this accelerator, another ... the switching magnet the tritium ions are counted with a surface barrier detector. .... AMS has been successfully applied to depth profiling of tritium in graphite ...

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

    Czech Academy of Sciences Publication Activity Database

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

    2005-01-01

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

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

    International Nuclear Information System (INIS)

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

    2006-01-01

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

  12. EFFECTS OF TRITIUM GAS EXPOSURE ON EPDM ELASTOMER

    Energy Technology Data Exchange (ETDEWEB)

    Clark, E.

    2009-12-11

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

  13. High-sensitivity mass spectrometry with a tandem accelerator

    International Nuclear Information System (INIS)

    Henning, W.

    1984-01-01

    The characteristic features of accelerator mass spectrometry are discussed. A short overview is given of the current status of mass spectrometry with high-energy (MeV/nucleon) heavy-ion accelerators. Emphasis is placed on studies with tandem accelerators and on future mass spectrometry of heavier isotopes with the new generation of higher-voltage tandems

  14. Tritium target performance during an LBLOCA in a PWR

    International Nuclear Information System (INIS)

    Reid, B.D.

    1996-01-01

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

  15. Effect of Tritium on Cracking Threshold in 7075 Aluminum

    Energy Technology Data Exchange (ETDEWEB)

    Duncan, A. [Savannah River Site (SRS), Aiken, SC (United States). Savannah River National Lab. (SRNL); Morgan, M. [Savannah River Site (SRS), Aiken, SC (United States). Savannah River National Lab. (SRNL)

    2017-02-28

    The effect of long-term exposure to tritium gas on the cracking threshold (KTH) of 7075 Aluminum Alloy was investigated. The alloy is the material of construction for a cell used to contain tritium in an accelerator at Jefferson Laboratory designed for inelastic scattering experiments on nucleons. The primary safety concerns for the Jefferson Laboratory tritium cell is a tritium leak due to mechanical failure of windows from hydrogen isotope embrittlement, radiation damage, or loss of target integrity from accidental excessive beam heating due to failure of the raster or grossly mis-steered beam. Experiments were conducted to investigate the potential for embrittlement of the 7075 Aluminum alloy from tritium gas.

  16. Effects of tritium in elastomers

    International Nuclear Information System (INIS)

    Zapp, P.E.

    1982-01-01

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

  17. New results from the Mainz neutrino mass experiment and perspective of a new large tritium-β-spectrometer

    International Nuclear Information System (INIS)

    Bonn, J.; Bornschein, B.; Bornschein, L.; Fickinger, L.; Kraus, Ch.; Otten, E.W.; Ulrich, H.; Weinheimer, Ch.; Kazachenko, O.; Kovalik, A.

    2001-01-01

    The Mainz neutrino mass experiment investigates the endpoint region of the tritium β decay spectrum to determine the mass of the electron antineutrino. By the recent upgrade the former problem of de-wetting T 2 films has been solved and the signal-to-background-ratio was improved by a factor of 10. The latest measurement leads to m ν 2 = -1.1 ± 2.6 stat ± 1.8 sys eV 2 /c 4 (preliminary), which corresponds to an upper limit of m ν 2 (95 % C.L.) (preliminary). Some indication for the anomaly, reported by the Troitsk group, was found, but its postulated half year period is contradicted by our data. The perspectives of a new Large Tritium-β-Spectrometer to reach sub eV sensitivity will be presented. (authors)

  18. Accelerator mass spectrometry at the Rossendorf 5 MV tandem accelerator

    International Nuclear Information System (INIS)

    Friedrich, M.; Buerger, W.; Curian, H.; Hartmann, B.; Hentschel, E.; Matthes, H.; Probst, W.; Seidel, M.; Turuc, S.; Hebert, D.; Rothe, T.; Stolz, W.

    1992-01-01

    The Rossendorf electrostatic accelerators (5 MV tandem accelerator and single ended 2 MV van de Graaff accelerator) are already used for ion beam analysis. The existing methods (RBS, PIXE, ERDA, NRA, nuclear microprobe and external beam) will be completed by introduction of Accelerator Mass Spectrometry (AMS). A short description of the Rossendorf AMS system is given and first experimental results are presented. (R.P.) 4 refs.; 6 figs

  19. Improved limit on the electron anti neutrino rest mass from tritium β decay

    International Nuclear Information System (INIS)

    Weinheimer, C.; Przyrembel, M.; Backe, H.; Barth, H.; Bonn, J.; Degen, B.; Edling, T.; Fischer, H.; Fleischmann, L.; Grooss, J.U.; Haid, R.; Hermanni, A.; Kube, G.; Loeken, T.; Molz, A.; Osipowicz, A.; Otten, E.W.; Picard, A.; Schrader, M.; Steininger, M.

    1993-01-01

    This paper presents the results of a re-measurement of the endpoint region of the beta-spectrum of tritium by an electrostatic spectrometer with magnetic guiding field. It enables the search for a rest mass of the electron anti neutrino with improved precision. The result is: m ν 2 =(-39±34 stat ±15 syst ) (eV/c 2 ) 2 , from which an upper limit of: m ν 2 may be derived. The experiment yields the atomic mass difference: m(T)-m( 3 He)=(18591±3) eV/c 2 . (TEC). 31 refs., 4 figs., 3 tabs

  20. Dose from organically bound tritium after an acute tritiated water intake in humans

    Energy Technology Data Exchange (ETDEWEB)

    Trivedi, A; Richardson, R B; Galeriu, D [Atomic Energy of Canada Ltd., Chalk River, ON (Canada). Chalk River Nuclear Labs.

    1995-10-01

    We have analyzed the urinary excretion data from eight male workers following an acute intake of tritiated water (HTO) and assessed the dose contribution from organically bound tritium (OBT) in the body. The individuals affected increased their fluid intakes during the first month or more post-exposure, to accelerate the turnover of tritium in the body water for dose mitigation purposes. The volumes of cumulative 24 h urine samples were similar to Reference Man in the latter part of the study (100-300 d post-exposure). The workers` urine samples were analyzed for total tritium up to 300 d post-exposure. The results suggest that a measurement of the tritium activity per unit mass of organic matter in urine can provide an assessment of the specific activity of tritium in the organic fraction of the soft tissue, providing an equilibrium condition exists. A mathematical model is proposed to estimate the dose increase from the retained OBT by examining the kinetics of total tritium excretion in urine. The model accounts for the variable rates of fluid intake. The influence of measurement errors and the limited duration of the study (0-300 d post-exposure) on the OBT dose contribution was assessed through statistical analysis, while the role of direct OBT excretion in urine was estimated by using metabolic models. Based on the time series of tritium concentration in urine, the average dose increase to the workers from the metabolised OBT was calculated as 6.2 {+-} 1.3% of the HTO dose. 78 refs., 36 tabs., 11 figs.

  1. Dose from organically bound tritium after an acute tritiated water intake in humans

    International Nuclear Information System (INIS)

    Trivedi, A.; Richardson, R.B.; Galeriu, D.

    1995-10-01

    We have analyzed the urinary excretion data from eight male workers following an acute intake of tritiated water (HTO) and assessed the dose contribution from organically bound tritium (OBT) in the body. The individuals affected increased their fluid intakes during the first month or more post-exposure, to accelerate the turnover of tritium in the body water for dose mitigation purposes. The volumes of cumulative 24 h urine samples were similar to Reference Man in the latter part of the study (100-300 d post-exposure). The workers' urine samples were analyzed for total tritium up to 300 d post-exposure. The results suggest that a measurement of the tritium activity per unit mass of organic matter in urine can provide an assessment of the specific activity of tritium in the organic fraction of the soft tissue, providing an equilibrium condition exists. A mathematical model is proposed to estimate the dose increase from the retained OBT by examining the kinetics of total tritium excretion in urine. The model accounts for the variable rates of fluid intake. The influence of measurement errors and the limited duration of the study (0-300 d post-exposure) on the OBT dose contribution was assessed through statistical analysis, while the role of direct OBT excretion in urine was estimated by using metabolic models. Based on the time series of tritium concentration in urine, the average dose increase to the workers from the metabolised OBT was calculated as 6.2 ± 1.3% of the HTO dose. 78 refs., 36 tabs., 11 figs

  2. Design of a tritium pellet injector for TFTR

    International Nuclear Information System (INIS)

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

    1991-01-01

    The TFTR tritium pellet injector (TPI) is designed to provide a tritium pellet fueling capability with pellet speeds in the 1- to 3 km/s-range for the TFTR D-T phase. The existing TFTR deuterium pellet injector is being modified at Oak Ridge National Laboratory to provide a fourshot, tritium-compatible, pipe-gun configuration with three upgraded single-stage pneumatic guns a two -stage light gas gun driver. The pipe gun concept has been qualified for tritium operation by the tritium proof-of-principle injector experiments conducted on the Tritium Systems Test Assembly at Los Alamos National Laboratory. In these experiments, tritium and D-T pellets were accelerated to speeds near 1.5 km/s. The TPI is being designed for pellet sizes in the range from 3.43 to 4.0 mm in diameter in arbitrarily programmable firing sequences at speeds up to approximately 1.5 km/s for the three single-stage drivers and 2.5 to 3 km/s for the two-stage driver. Injector operation will be controlled by a programmable logic controller. 7 refs., 4 figs

  3. 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.)

  4. A new technique of ion beam tritium labelling

    International Nuclear Information System (INIS)

    Zhang Nianbao; Sheng Shugang; Yao Fuzeng

    1990-01-01

    In this paper a new technique is reported for tritium labelling of proteins, peptides and other nonvolatile organic compounds. A tritium ion beam is accelerated to bombard solid sample target for producing tritium exchange with hydrogen. The tritium labelling method has been applied to tritiated soybean trypsin inhibitor, ribonuclease A, elastin, pachyman and others totalled 11. After purifying by dialysis, ion exchange chromatography and gel filtration, the tritiated proteins and polysaccharide were obtained with specific activity over 37 GBq/mmol, without decomposition and with biological activity well preserved. By amino acid analysis of tritiated protein it was shown that the relative specific radioactivities for His., Tyr. and Phe. residues were higher while those for Val., Ile. and Ser. residues were lower

  5. Surface Mass Balance Contributions to Acceleration of Antarctic Ice Mass Loss during 2003- 2013

    Science.gov (United States)

    Seo, K. W.; Wilson, C. R.; Scambos, T. A.; Kim, B. M.; Waliser, D. E.; Tian, B.; Kim, B.; Eom, J.

    2015-12-01

    Recent observations from satellite gravimetry (the GRACE mission) suggest an acceleration of ice mass loss from the Antarctic Ice Sheet (AIS). The contribution of surface mass balance changes (due to variable precipitation) is compared with GRACE-derived mass loss acceleration by assessing the estimated contribution of snow mass from meteorological reanalysis data. We find that over much of the continent, the acceleration can be explained by precipitation anomalies. However, on the Antarctic Peninsula and other parts of West Antarctica mass changes are not explained by precipitation and are likely associated with ice discharge rate increases. The total apparent GRACE acceleration over all of the AIS between 2003 and 2013 is -13.6±7.2 GTon/yr2. Of this total, we find that the surface mass balance component is -8.2±2.0 GTon/yr2. However, the GRACE estimate appears to contain errors arising from the atmospheric pressure fields used to remove air mass effects. The estimated acceleration error from this effect is about 9.8±5.8 GTon/yr2. Correcting for this yields an ice discharge acceleration of -15.1±6.5 GTon/yr2.

  6. Improved limit on the mass of ν/sub e/ from the beta decay of molecular tritium

    International Nuclear Information System (INIS)

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

    1989-01-01

    We report a new upper limit of 13.4 eV (95% confidence level) on the mass of the electron antineutrino from a study of the shape of the beta spectrum of free molecular tritium. This result appears to be inconsistent with a reported value for the mass of 26(5) eV. The electron neutrino is evidently not massive enough to close the universe by itself. 23 refs., 1 fig., 2 tabs

  7. Improved limit on the mass of bar νe from the beta decay of molecular tritium

    International Nuclear Information System (INIS)

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

    1990-01-01

    We report a new upper limit of 13.4 eV (95% confidence level) on the mass of the electron antineutrino from a study of the shape of the beta spectrum of free molecular tritium. This result appears to be inconsistent with a reported value for the mass of 26(5) eV. The electron neutrino is evidently not massive enough to close the universe by itself. 21 refs., 1 fig., 2 tabs

  8. Surface mass balance contributions to acceleration of Antarctic ice mass loss during 2003-2013

    OpenAIRE

    Seo, Ki-Weon; Wilson, Clark R.; Scambos, Ted; Kim, Baek-Min; Waliser, Duane E.; Tian, Baijun; Kim, Byeong-Hoon; Eom, Jooyoung

    2015-01-01

    Abstract Recent observations from satellite gravimetry (the Gravity Recovery and Climate Experiment (GRACE) mission) suggest an acceleration of ice mass loss from the Antarctic Ice Sheet (AIS). The contribution of surface mass balance changes (due to variable precipitation) is compared with GRACE?derived mass loss acceleration by assessing the estimated contribution of snow mass from meteorological reanalysis data. We find that over much of the continent, the acceleration can be explained by ...

  9. Status of tritium technology development for magnetic-fusion energy

    International Nuclear Information System (INIS)

    Anderson, J.L.

    1983-01-01

    The development of tritium technology for the magnetic fusion energy program has progressed at a rapid rate over the past two years. The focal points for this development in the United States have been the Tritium Systems Test Assembly at Los Alamos and the FED/INTOR studies supported by the Fusion Engineering Design Center at Oak Ridge. In Canada the Canadian Fusion Fuel Technology Project has been initiated and promises to make significant contributions to the tritium technology program in the next few years. The Japanese government has now approved funding for the Tritium Processing Laboratory at the Japan Atomic Energy Research Institute's Tokai Research Establishment. Construction on this new facility is scheduled to begin in April 1983. This facility will be the center for fusion tritium technology development in Japan. The European Community is currently working on the design of the tritium facility for the Joint European Torus. There is considerable interaction between all of these programs, thus accelerating the overall development of this crucial technology

  10. High intensity linear accelerator development topics for panel discussion on ''Nuclear Energy Research and Accelerators: Future Prospects''

    International Nuclear Information System (INIS)

    Jameson, R.A.

    1989-01-01

    Two companion papers at this meeting have introduced the subject of high intensity linacs for materials research and for radioactive waste transmutation; Prof. Kaneko's paper ''Intense Proton Accelerator,'' and my paper ''Accelerator-Based Intense Neutron Source for Materials R ampersand D.'' I will expand on those remarks to briefly outline some of the extensive work that has been done at Los Alamos toward those two application areas, plus a third --- the production of tritium in an accelerator-based facility (APT--Accelerator Production of Tritium). 1 ref., 11 figs

  11. Atom counting with accelerator mass spectrometry

    International Nuclear Information System (INIS)

    Kutschera, Walter

    1995-01-01

    A brief review of the current status and some recent applications of accelerator mass spectrometry (AMS) are presented. Some connections to resonance ionization mass spectroscopy (RIS) as the alternate atom counting method are discussed

  12. Accelerator mass spectrometry-current status in techniques and applications

    International Nuclear Information System (INIS)

    Imamura, Mineo; Nagai, Hisao; Kobayashi, Koichi.

    1991-01-01

    Accelerator mass spectrometry (AMS) is the mass spectrometry by incorporating an accelerator. After samples are ionized, they are accelerated to a certain energy, and mass, energy, nuclear charge (atomic number) are distinguished, and ion counting is made one by one with a heavy ion detector. For the measurement of long half-life radioisotopes, mass spectrometry has been used because of the high sensitivity, but in low energy mass spectrometry, there are the difficulties due to the mixing of the molecular ions having nearly same mass and the existence of isobars. One of the methods solving these difficulties is an accelerator which enables background-free measurement. The progress of AMS is briefly described, and at present, it is carried out in about 30 facilities in the world. In AMS, the analysis is carried out in the order of the ionization of samples, the acceleration of beam, the electron stripping with a thin film, the sorting of the momentum and energy of beam and the identification of particles. The efficiency, sensitivity and accuracy of detection and the application are reported. (K.I.)

  13. 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)

  14. 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)

  15. APT accelerator. Topical report

    International Nuclear Information System (INIS)

    Lawrence, G.; Rusthoi, D.

    1995-03-01

    The Accelerator Production of Tritium (APT) project, sponsored by Department of Energy Defense Programs (DOE/DP), involves the preconceptual design of an accelerator system to produce tritium for the nation's stockpile of nuclear weapons. Tritium is an isotope of hydrogen used in nuclear weapons, and must be replenished because of radioactive decay (its half-life is approximately 12 years). Because the annual production requirements for tritium has greatly decreased since the end of the Cold War, an alternative approach to reactors for tritium production, based on a linear accelerator, is now being seriously considered. The annual tritium requirement at the time this study was undertaken (1992-1993) was 3/8 that of the 1988 goal, usually stated as 3/8-Goal. Continued reduction in the number of weapons in the stockpile has led to a revised (lower) production requirement today (March, 1995). The production requirement needed to maintain the reduced stockpile, as stated in the recent Nuclear Posture Review (summer 1994) is approximately 3/16-Goal, half the previous level. The Nuclear Posture Review also requires that the production plant be designed to accomodate a production increase (surge) to 3/8-Goal capability within five years, to allow recovery from a possible extended outage of the tritium plant. A multi-laboratory team, collaborating with several industrial partners, has developed a preconceptual APT design for the 3/8-Goal, operating at 75% capacity. The team has presented APT as a promising alternative to the reactor concepts proposed for Complex-21. Given the requirements of a reduced weapons stockpile, APT offers both significant safety, environmental, and production-fexibility advantages in comparison with reactor systems, and the prospect of successful development in time to meet the US defense requirements of the 21st Century

  16. APT accelerator. Topical report

    Energy Technology Data Exchange (ETDEWEB)

    Lawrence, G.; Rusthoi, D. [comp.] [ed.

    1995-03-01

    The Accelerator Production of Tritium (APT) project, sponsored by Department of Energy Defense Programs (DOE/DP), involves the preconceptual design of an accelerator system to produce tritium for the nation`s stockpile of nuclear weapons. Tritium is an isotope of hydrogen used in nuclear weapons, and must be replenished because of radioactive decay (its half-life is approximately 12 years). Because the annual production requirements for tritium has greatly decreased since the end of the Cold War, an alternative approach to reactors for tritium production, based on a linear accelerator, is now being seriously considered. The annual tritium requirement at the time this study was undertaken (1992-1993) was 3/8 that of the 1988 goal, usually stated as 3/8-Goal. Continued reduction in the number of weapons in the stockpile has led to a revised (lower) production requirement today (March, 1995). The production requirement needed to maintain the reduced stockpile, as stated in the recent Nuclear Posture Review (summer 1994) is approximately 3/16-Goal, half the previous level. The Nuclear Posture Review also requires that the production plant be designed to accomodate a production increase (surge) to 3/8-Goal capability within five years, to allow recovery from a possible extended outage of the tritium plant. A multi-laboratory team, collaborating with several industrial partners, has developed a preconceptual APT design for the 3/8-Goal, operating at 75% capacity. The team has presented APT as a promising alternative to the reactor concepts proposed for Complex-21. Given the requirements of a reduced weapons stockpile, APT offers both significant safety, environmental, and production-fexibility advantages in comparison with reactor systems, and the prospect of successful development in time to meet the US defense requirements of the 21st Century.

  17. Construction and operation of a tritium extraction facility at the Savannah River Site. Final environmental impact statement

    International Nuclear Information System (INIS)

    1999-03-01

    DOE proposes to construct and operate a Tritium Extraction Facility (TEF) at H Area on the Savannah River Site (SRS) to provide the capability to extract tritium from commercial light water reactor (CLWR) targets and from targets of similar design. The proposed action is also DOE's preferred alternative. An action alternative is to construct and operate TEF at the Allied General Nuclear Services facility, which is adjacent to the eastern side of the SRS. Under the no-action alternative DOE could incorporate tritium extraction capabilities in the accelerator for production of tritium. This EIS is linked to the Final Programmatic Environmental Impact Statement for Tritium Supply and Recycling, from which DOE determined that it would produce tritium either in an accelerator or in a commercial light water reactor. The purpose of the proposed action and alternatives evaluated in this EIS is to provide tritium extraction capability to support either tritium production technology. The EIS assesses the environmental impacts from the proposed action and the alternatives, including the no action alternative

  18. Tritium Assay and Dispensing of KEPRI Tritium Lab

    International Nuclear Information System (INIS)

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

    2009-01-01

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

  19. Accelerator mass spectrometry and associated facilities at Inter-University Accelerator Centre, New Delhi, India

    International Nuclear Information System (INIS)

    Kumar, Pankaj; Bohra, Archna; Ojha, S.; Gargari, S.; Joshi, R.; Roonwal, G.S.; Chopra, S.; Pattanaik, J.K.; Balakrishnan, S.

    2011-01-01

    Accelerator Mass Spectrometry (AMS) facility at Inter-University Accelerator Centre (IUAC) is developed by upgrading its existing 15UD Pelletron accelerator. Since last two decades Pelletron is mainly used for nuclear physics, materials science, atomic physics, radiation biology and accelerator mass spectrometry is recent development. In addition, a chemistry laboratory in clean room for the chemical processing of samples for AMS studies has also been established. At present the AMS facility is used for 10 Be, 26 Al measurements and soon other long lived radio-isotopes will also be used

  20. Analytic of tritium-containing gaseous species at the Tritium Laboratory Karlsruhe

    International Nuclear Information System (INIS)

    Laesser, R.; Caldwell-Nichols, C.; Doerr, L.; Glugla, M.; Gruenhagen, S.; Guenther, K.; Penzhorn, R.-D.

    2001-01-01

    At the Tritium Laboratory Karlsruhe (TLK) laser Raman spectroscopy, gas chromatography, mass spectroscopy, calorimetry and ionisation chambers are used to determine the composition of tritium gas mixtures. For the first time a laser Raman experiment was assembled with an actively controlled resonator which yields a 50 times higher Raman signal and with all components (laser, optics, Raman cell and spectrometer) installed inside a glove box. Three gas chromatographs, each with up to six detectors, can determine the gases and their tritiated fractions expected in fusion devices down to the sub-ppm range. Tritium in solids, liquids and gases is determined by means of three calorimeters with a dynamic ranges of up to five orders of magnitude and a lower detection limit of 1 GBq. Since any of these techniques has its shortcomings the best analytical approach is to analyse a sample by more than one method

  1. 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.

  2. 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

  3. Accelerator Production of Tritium project process waste assessment

    Energy Technology Data Exchange (ETDEWEB)

    Carson, S.D.; Peterson, P.K.

    1995-09-01

    DOE has made a commitment to compliance with all applicable environmental regulatory requirements. In this respect, it is important to consider and design all tritium supply alternatives so that they can comply with these requirements. The management of waste is an integral part of this activity and it is therefore necessary to estimate the quantities and specific wastes that will be generated by all tritium supply alternatives. A thorough assessment of waste streams includes waste characterization, quantification, and the identification of treatment and disposal options. The waste assessment for APT has been covered in two reports. The first report was a process waste assessment (PWA) that identified and quantified waste streams associated with both target designs and fulfilled the requirements of APT Work Breakdown Structure (WBS) Item 5.5.2.1. This second report is an expanded version of the first that includes all of the data of the first report, plus an assessment of treatment and disposal options for each waste stream identified in the initial report. The latter information was initially planned to be issued as a separate Waste Treatment and Disposal Options Assessment Report (WBS Item 5.5.2.2).

  4. Accelerator Production of Tritium project process waste assessment

    International Nuclear Information System (INIS)

    Carson, S.D.; Peterson, P.K.

    1995-09-01

    DOE has made a commitment to compliance with all applicable environmental regulatory requirements. In this respect, it is important to consider and design all tritium supply alternatives so that they can comply with these requirements. The management of waste is an integral part of this activity and it is therefore necessary to estimate the quantities and specific wastes that will be generated by all tritium supply alternatives. A thorough assessment of waste streams includes waste characterization, quantification, and the identification of treatment and disposal options. The waste assessment for APT has been covered in two reports. The first report was a process waste assessment (PWA) that identified and quantified waste streams associated with both target designs and fulfilled the requirements of APT Work Breakdown Structure (WBS) Item 5.5.2.1. This second report is an expanded version of the first that includes all of the data of the first report, plus an assessment of treatment and disposal options for each waste stream identified in the initial report. The latter information was initially planned to be issued as a separate Waste Treatment and Disposal Options Assessment Report (WBS Item 5.5.2.2)

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

    Energy Technology Data Exchange (ETDEWEB)

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

    1998-03-01

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

  6. The APT program plan: Providing an assured tritium production capability

    International Nuclear Information System (INIS)

    Lisowski, P.W.; Anderson, J.L.; Bishop, W.P.; Boggs, B.; Hall, K.

    1996-01-01

    Tritium is a radioactive hydrogen isotope used in all U.S. nuclear weapons. Because the half-life of tritium is short, 12.3 yr, it must be periodically replenished. To provide a new source, the U.S. Department of Energy (DOE) is sponsoring conceptual design and engineering development and demonstration activities for a plant that will use a high-power proton linear accelerator to produce tritium and will go on-line no later than 2007. The APT project is in the process of completing the conceptual design for a tritium production plant. In addition, there are several important areas under engineering development and demonstration that will ensure an efficient, cost-effective plant design and provide an adequate margin of tritium production. Information provided from this work will be used by the DOE in its 1998 choice of production technology implementation

  7. Draft programmatic environmental impact statement for tritium supply and recycling

    International Nuclear Information System (INIS)

    1995-02-01

    Tritium, a radioactive gas used in all of the Nation's nuclear weapons, has a short half-life and must be replaced periodically in order for the weapon to operate as designed. Currently, the Nation has no tritium production capability. The Tritium Supply and Recycling PEIS evaluates the alternatives for the siting, construction, and operation of tritium supply and recycling facilities at each of five candidate sites: the Idaho Engineering Laboratory, the Nevada Test Site, the Oak Ridge Reservation, the Pantex Plant, and the Savannah River Site. Alternatives for new tritium supply and recycling facilities consist of four different tritium supply technologies; Heavy Water Reactor, Modular High Temperature Gas-cooled Reactor, Advanced Light Water Reactor, and Accelerator Production of Tritium. The PEIS also evaluates the impacts of using a commercial light water reactor, either as a contingency in the event of a national emergency or if purchased by the DOE and converted to defense purposes. Additionally, the PEIS includes an analysis of multi-purpose reactors which would produce tritium, dispose of plutonium and produce electricity. Volume I contains the findings of these analyses, Volume II contains the Appendices and supporting data

  8. 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.)

  9. Tritium Mitigation/Control for Advanced Reactor System

    Energy Technology Data Exchange (ETDEWEB)

    Sun, Xiaodong; Christensen, Richard; Saving, John P

    2018-03-31

    A tritium removal facility, which is similar to the design used for tritium recovery in fusion reactors, is proposed in this study for fluoride-salt-cooled high-temperature reactors (FHRs) to result in a two-loop FHR design with the elimination of an intermediate loop. Using this approach, an economic benefit can potentially be obtained by removing the intermediate loop, while the safety concern of tritium release can be mitigated. In addition, an intermediate heat exchanger (IHX) that can yield a similar tritium permeation rate to the production rate of 1.9 Ci/day in a 1,000 MWe PWR needs to be designed to prevent the residual tritium that is not captured in the tritium removal system from escaping into the power cycle and ultimately the environment. The main focus of this study is to aid the mitigation of tritium permeation issue from the FHR primary side to significantly reduce the concentration of tritium in the secondary side and the process heat application side (if applicable). The goal of the research is to propose a baseline FHR system without the intermediate loop. The specific objectives to accomplish the goals are: 1. To estimate tritium permeation behavior in FHRs; 2. To design a tritium removal system for FHRs; 3. To meet the same tritium permeation level in FHRs as the tritium production rate of 1.9 Ci/day in 1,000 MWe PWRs; 4. To demonstrate economic benefits of the proposed FHR system via comparing with the three-loop FHR system. The objectives were accomplished by designing tritium removal facilities, developing a tritium analysis code, and conducting an economic analysis. In the fusion reactor community, tritium extraction has been widely investigated and researched. Borrowing the experiences from the fusion reactor community, a tritium control and mitigation system was proposed. Based on mass transport theories, a tritium analysis code was developed, and the tritium behaviors were analyzed using the developed code. Tritium removal facilities

  10. Evaluation of medical isotope production with the accelerator production of tritium (APT) facility

    International Nuclear Information System (INIS)

    Benjamin, R.W.; Frey, G.D.; McLean, D.C., Jr; Spicer, K.M.; Davis, S.E.; Baron, S.; Frysinger, J.R.; Blanpied, G.; Adcock, D.

    1997-01-01

    The accelerator production of tritium (APT) facility, with its high beam current and high beam energy, would be an ideal supplier of radioisotopes for medical research, imaging, and therapy. By-product radioisotopes will be produced in the APT window and target cooling systems and in the tungsten target through spallation, neutron, and proton interactions. High intensity proton fluxes are potentially available at three different energies for the production of proton- rich radioisotopes. Isotope production targets can be inserted into the blanket for production of neutron-rich isotopes. Currently, the major production sources of radioisotopes are either aging or abroad, or both. The use of radionuclides in nuclear medicine is growing and changing, both in terms of the number of nuclear medicine procedures being performed and in the rapidly expanding range of procedures and radioisotopes used. A large and varied demand is forecast, and the APT would be an ideal facility to satisfy that demand

  11. Design of a ram accelerator mass launch system

    Science.gov (United States)

    Aarnio, Michael; Armerding, Calvin; Berschauer, Andrew; Christofferson, Erik; Clement, Paul; Gohd, Robin; Neely, Bret; Reed, David; Rodriguez, Carlos; Swanstrom, Fredrick

    1988-01-01

    The ram accelerator mass launch system has been proposed to greatly reduce the costs of placing acceleration-insensitive payloads into low earth orbit. The ram accelerator is a chemically propelled, impulsive mass launch system capable of efficiently accelerating relatively large masses from velocities of 0.7 km/sec to 10 km/sec. The principles of propulsion are based on those of a conventional supersonic air-breathing ramjet; however the device operates in a somewhat different manner. The payload carrying vehicle resembles the center-body of the ramjet and accelerates through a stationary tube which acts as the outer cowling. The tube is filled with premixed gaseous fuel and oxidizer mixtures that burn in the vicinity of the vehicle's base, producing a thrust which accelerates the vehicle through the tube. This study examines the requirement for placing a 2000 kg vehicle into a 500 km circular orbit with a minimum amount of on-board rocket propellant for orbital maneuvers. The goal is to achieve a 50 pct payload mass fraction. The proposed design requirements have several self-imposed constraints that define the vehicle and tube configurations. Structural considerations on the vehicle and tube wall dictate an upper acceleration limit of 1000 g's and a tube inside diameter of 1.0 m. In-tube propulsive requirements and vehicle structural constraints result in a vehicle diameter of 0.76 m, a total length of 7.5 m and a nose-cone half angle of 7 degrees. An ablating nose-cone constructed from carbon-carbon composite serves as the thermal protection mechanism for atmospheric transit.

  12. Calibration of a liquid scintillation counter to assess tritium levels in various samples

    CERN Document Server

    Al-Haddad, M N; Abu-Jarad, F A

    1999-01-01

    An LKB-Wallac 1217 Liquid Scintillation Counter (LSC) was calibrated with a newly adopted cocktail. The LSC was then used to measure tritium levels in various samples to assess the compliance of tritium levels with the recommended international levels. The counter was calibrated to measure both biological and operational samples for personnel and for an accelerator facility at KFUPM. The biological samples include the bioassay (urine), saliva, and nasal tests. The operational samples of the light ion linear accelerator include target cooling water, organic oil, fomblin oil, and smear samples. Sets of standards, which simulate various samples, were fabricated using traceable certified tritium standards. The efficiency of the counter was obtained for each sample. The typical range of the efficiencies varied from 33% for smear samples down to 1.5% for organic oil samples. A quenching curve for each sample is presented. The minimum detectable activity for each sample was established. Typical tritium levels in bio...

  13. Materials considerations in accelerator targets

    International Nuclear Information System (INIS)

    Peacock, H.B. Jr.; Iyer, N.C.; Louthan, M.R. Jr.

    1994-01-01

    Future nuclear materials production and/or the burn-up of long lived radioisotopes may be accomplished through the capture of spallation produced neutrons in accelerators. Aluminum clad-lead and/or lead alloys has been proposed as a spallation target. Aluminum was the cladding choice because of the low neutron absorption cross section, fast radioactivity decay, high thermal conductivity, and excellent fabricability. Metallic lead and lead oxide powders were considered for the target core with the fabrication options being casting or powder metallurgy (PM). Scoping tests to evaluate gravity casting, squeeze casting, and casting and swaging processes showed that, based on fabricability and heat transfer considerations, squeeze casting was the preferred option for manufacture of targets with initial core cladding contact. Thousands of aluminum clad aluminum-lithium alloy core targets and control rods for tritium production have been fabricated by coextrusion processes and successfully irradiated in the SRS reactors. Tritium retention in, and release from the coextruded product was modeled from experimental and operational data. Newly produced tritium atoms were trapped by lithium atoms to form a lithium tritide. The effective tritium pressure required for trap or tritide stability was the equilibrium decomposition pressure of tritium over a lithium tritide-aluminum mixture. The temperature dependence of tritium release was determined by the permeability of the cladding to tritium and the local equilibrium at the trap sites. The model can be used to calculate tritium release from aluminum clad, aluminum-lithium alloy targets during postulated accelerator operational and accident conditions. This paper describes the manufacturing technologies evaluated and presents the model for tritium retention in aluminum clad, aluminum-lithium alloy tritium production targets

  14. Energy behaviour of neutrons generated by Witch-type distributed axi-symmetrical deuteron beams accelerated onto plane tritium targets

    International Nuclear Information System (INIS)

    Timus, D.M.; Bradley, D.A.; Timus, B.D.; Kalla, S.L.; Srivastava, H.M.

    2000-01-01

    This paper is an analytical study of the spatial dependency of the d-T neutron energy in the vicinity of a homogeneous tritium-occluded plane target. Close to the target, and along the path of incidence of axially symmetric deuteron beams, the transverse density of accelerated deuterons is assumed to be governed by a law approximated by the 'Witch' function. In particular circumstances, the elementary neutron emission process in non-dispersive media can be considered to be omni-directional (due consideration being paid to collision kinetics, depending upon mass and kinetic energy of particles involved in the nuclear collision, nuclear reaction energy, etc.). Consequently, analytical expressions can be considerably simplified. By applying the classical kinetic energy and momentum conservation laws to nuclear processes, a theoretical description is obtained, taking into account the exoergic character of d-T fusion reaction. A number of expressions for energetic prediction of the fast neutron field are proposed. The associated relations, involving elementary functions, can be investigated using a desk-top computer. Computationally tractable tools are of importance in the study of diverse situations such as induced reactions and activation analysis using 14 MeV neutron generators, investigations in health-physics, radiation dose measurements, nuclear medicine, damage effects, and simulation studies

  15. Low energy demonstration accelerator technical area 53

    International Nuclear Information System (INIS)

    1996-01-01

    As part of the Department of Energy's (DOE) need to maintain the capability of producing tritium in support of its historic and near-term stewardship of the nation's nuclear weapons stockpile, the agency has recently completed a Programmatic Environmental Impact Statement for Tritium Supply and Recycling. The resulting Record of Decision (ROD) determined that over the next three years the DOE would follow a dual-track acquisition strategy that assures tritium production for the nuclear weapon stockpile in a rapid, cost effective, and safe manner. Under this strategy the DOE will further investigate and compare two options for producing tritium: (1) purchase of an existing commercial light-water reactor or irradiation services with an option to purchase the reactor for conversion to a defense facility; and (2) design, build, and test critical components of a system for accelerator production of tritium (APT). The final decision to select the primary production option will be made by the Secretary of Energy in the October 1998 time frame. The alternative not chosen as the primary production method, if feasible, would be developed as a back-up tritium supply source. This Environmental Assessment (EA) analyzes the potential environmental effects that would be expected to occur if the DOE were to design, build, and test critical prototypical components of the accelerator system for tritium production, specifically the front-end low-energy section of the accelerator, at Los Alamos National Laboratory. The Low Energy Demonstration Accelerator (LEDA) would be incrementally developed and tested in five separate stages over the next seven years. The following issues were evaluated for the proposed action: utility demands, air, human health, environmental restoration, waste management, transportation, water, threatened and endangered species, wetlands, cultural resources, and environmental justice

  16. Acceleration of tritons with a compact cyclotron

    International Nuclear Information System (INIS)

    Wegmann, H.; Huenges, E.; Muthig, H.; Moringa, H.

    1981-01-01

    With the compact cyclotron at the Faculty of Physics of the Technical University of Munich, tritons have been accelerated to an energy of 7 MeV. A safe and reliable operation of the gas supply for the ion source was obtained by a new tritium storage system. A quantity of 1500 Ci tritium is stored by two special Zr-Al getter pumps in a non-gaseous phase. The tritium can be released in well-defined amounts by heating the getter material. During triton acceleration the pressure in the cyclotron vacuum chamber is maintained only by a large titanium sputter-ion pump, thus forming a closed vacuum system without any exhaust of tritium contaminated gas. Any tritium contaminations in the air can be detected by an extremely sensitive tritium monitoring system. The triton beam with a maximum intensity of 30 μA has been used so far to produce neutron-rich radioisotopes such as 28 Mg, 43 K, or 72 Zn, which are successfully applied in tracer techniques in the studies of biological systems. (orig.)

  17. Japanese university program on tritium radiobiology and environmental tritium

    International Nuclear Information System (INIS)

    Okada, Shigefumi

    1989-01-01

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

  18. McMaster Accelerator Laboratory annual report, 1984

    International Nuclear Information System (INIS)

    1984-11-01

    Summaries of projects in progress constitute the major portion of this report. The tandem accelerator operated well during most of the year, with a number of heavy ion runs carried out at 10.44 MV. Tritium beams and polarized deuteron beams have been used extensively. Experiments using the multiplicity filter to study high spin states continue. An experiment was carried out relating to the search for a neutrino mass. Activity also continued in other areas of physics, engineering and medicine

  19. Materials considerations in accelerator targets

    International Nuclear Information System (INIS)

    Peacock, H. B. Jr.; Iyer, N. C.; Louthan, M. R. Jr.

    1995-01-01

    Future nuclear materials production and/or the burn-up of long lived radioisotopes may be accomplished through the capture of spallation produced neutrons in accelerators. Aluminum clad-lead and/or lead alloys has been proposed as a spallation target. Aluminum was the cladding choice because of the low neutron absorption cross section, fast radioactivity decay, high thermal conductivity, and excellent fabricability. Metallic lead and lead oxide powders were considered for the target core with the fabrication options being casting or powder metallurgy (PM). Scoping tests to evaluate gravity casting, squeeze casting, and casting and swaging processes showed that, based on fabricability and heat transfer considerations, squeeze casting was the preferred option for manufacture of targets with initial core cladding contact. Thousands of aluminum clad aluminum-lithium alloy core targets and control rods for tritium production have been fabricated by coextrusion processes and successfully irradiated in the SRS reactors. Tritium retention in, and release from, the coextruded product was modeled from experimental and operational data. The model assumed that tritium atoms, formed by the 6Li(n,a)3He reaction, were produced in solid solution in the Al-Li alloy. Because of the low solubility of hydrogen isotopes in aluminum alloys, the irradiated Al-Li rapidly became supersaturated in tritium. Newly produced tritium atoms were trapped by lithium atoms to form a lithium tritide. The effective tritium pressure required for trap or tritide stability was the equilibrium decomposition pressure of tritium over a lithium tritide-aluminum mixture. The temperature dependence of tritium release was determined by the permeability of the cladding to tritium and the local equilibrium at the trap sites. The model can be used to calculate tritium release from aluminum clad, aluminum-lithium alloy targets during postulated accelerator operational and accident conditions. This paper describes

  20. A new technique for ion beam tritium labelling

    International Nuclear Information System (INIS)

    Zhang Nianbao; Sheng Shugang; Yao Fuzeng

    1990-06-01

    An advanced technique, the ion beam tritium labelling method (IBTL), used for labelling proteins, peptides and other nonvolatile organic compounds is introduced. In this method the excited tritium ion beam is accelerated and then bombs a solid sample target in which tritium exchanging for hydrogen is taken place. The IBTL has been used for preparation of tritiated soybean trypsin inhibitor, ribonuclease A, elastin and pachyman etc. After purifing by dialysis, ion exchange chromatography and gel filtration, the tritiated proteins and polysaccharide were obtained with the specific activity over 37 GBq/mmol, the function of tritiated decomposition products was not found. The product was shown to have native biological activity. Amino acid analysis of tritiated protein showed that the relative specific radioactivities were higher for His., Tyr. and Phe. but lower for Val., Ile. and Ser

  1. Prospects for cosmic neutrino detection in tritium experiments in the case of hierarchical neutrino masses

    International Nuclear Information System (INIS)

    Blennow, Mattias

    2008-01-01

    We discuss the effects of neutrino mixing and the neutrino mass hierarchy when considering the capture of the cosmic neutrino background (CNB) on radioactive nuclei. The implications of mixing and hierarchy at future generations of tritium decay experiments are considered. We find that the CNB should be detectable at these experiments provided that the resolution for the kinetic energy of the outgoing electron can be pushed to a few 0.01 eV for the scenario with inverted neutrino mass hierarchy, about an order of magnitude better than that of the upcoming KATRIN experiment. Another order of magnitude improvement is needed in the case of normal neutrino mass hierarchy. We also note that mixing effects generally make the prospects for CNB detection worse due to an increased maximum energy of the normal beta decay background

  2. 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.

  3. Mass spectrometry with particle accelerator

    International Nuclear Information System (INIS)

    Anon.

    1983-01-01

    The heavy ion accelerator use is renewing the ultrasensitive mass spectrometry in extending the detection limits. These new devices allow the measurement of rare isotope ratio, as 10 Be, 14 C, 26 Al, 36 Cl or 41 Ca, from the earth natural reservoirs [fr

  4. Accelerator mass spectrometry: state of the art

    Energy Technology Data Exchange (ETDEWEB)

    Tuniz, C. [Australian Nuclear Science and Technology Organisation, Lucas Heights, NSW (Australia)

    1996-12-31

    Accelerator Mass Spectrometry (AMS) is the analytical technique of choice for the detection of long-lived radionuclides which cannot be practically analysed with decay counting or conventional mass spectrometry. The main use of AMS has been in the analysis of radiocarbon and other cosmogenic radionuclides for archaeological, geological and environmental applications. In addition, AMS has been recently applied in biomedicine to study exposure of human tissues to chemicals and biomolecules at attomole levels. There is also a world-wide effort to analyse rare nuclides of heavier masses, such as long-lived actinides, with important applications in safeguards and nuclear waste disposal. The use of AMS is limited by the expensive accelerator technology required and there are several attempts to develop smaller and cheaper AMS spectrometers. 5 refs.

  5. Accelerator mass spectrometry: state of the art

    Energy Technology Data Exchange (ETDEWEB)

    Tuniz, C [Australian Nuclear Science and Technology Organisation, Lucas Heights, NSW (Australia)

    1997-12-31

    Accelerator Mass Spectrometry (AMS) is the analytical technique of choice for the detection of long-lived radionuclides which cannot be practically analysed with decay counting or conventional mass spectrometry. The main use of AMS has been in the analysis of radiocarbon and other cosmogenic radionuclides for archaeological, geological and environmental applications. In addition, AMS has been recently applied in biomedicine to study exposure of human tissues to chemicals and biomolecules at attomole levels. There is also a world-wide effort to analyse rare nuclides of heavier masses, such as long-lived actinides, with important applications in safeguards and nuclear waste disposal. The use of AMS is limited by the expensive accelerator technology required and there are several attempts to develop smaller and cheaper AMS spectrometers. 5 refs.

  6. Final programmatic environmental impact statement for tritium supply and recycling

    International Nuclear Information System (INIS)

    1995-10-01

    Tritium, a radioactive gas used in all of the Nation's nuclear weapons, has a short half-life and must be replaced periodically in order for the weapon to operate as designed. Currently, there is no capability to produce the required amounts of tritium within the Nuclear Weapons Complex. The PEIS for Tritium Supply and Recycling evaluates the alternatives for the siting, construction, and operation of tritium supply and recycling facilities at each of five candidate sites: the Idaho National Engineering Laboratory, the Nevada Test Site, the Oak Ridge Reservation, the Pantex Plant, and the Savannah River Site. Alternatives for new tritium supply and recycling facilities consist of four different tritium supply technologies: Heavy Water Reactor, Modular High Temperature Gas-Cooled Reactor, Advanced Light Water Reactor, and Accelerator Production of Tritium. The PEIS also evaluates the impacts of the DOE purchase of an existing operating or partially completed commercial light water reactor or the DOE purchase of irradiation services contracted from commercial power reactors. Additionally, the PEIS includes an analysis of multipurpose reactors that would produce tritium, dispose of plutonium, and produce electricity. Evaluation of impacts on land resources, site infrastructure, air quality and acoustics, water resources, geology and soils, biotic resources, cultural and paleontological resources, socioeconomics, radiological and hazardous chemical impacts during normal operation and accidents to workers and the public, waste management, and intersite transport are included in the assessment

  7. APT related papers presented at the 1997 particle accelerator conference, Vancouver, May 12--16, 1997

    International Nuclear Information System (INIS)

    Lawrence, G.

    1997-07-01

    Tritium is essential for the US nuclear weapons to function, but because it is radioactive with a half-life of 12.3 years, the supply must be periodically replenished. Presently, only reactor or accelerator systems can be used to produce tritium. This report is a compilation of 31 papers given at the 1997 Particle Accelerator Conference which dealt with the accelerator production of tritium. The papers are grouped into two categories, invited and contributed

  8. APT related papers presented at the 1997 particle accelerator conference, Vancouver, May 12--16, 1997

    Energy Technology Data Exchange (ETDEWEB)

    Lawrence, G. [comp.

    1997-07-01

    Tritium is essential for the US nuclear weapons to function, but because it is radioactive with a half-life of 12.3 years, the supply must be periodically replenished. Presently, only reactor or accelerator systems can be used to produce tritium. This report is a compilation of 31 papers given at the 1997 Particle Accelerator Conference which dealt with the accelerator production of tritium. The papers are grouped into two categories, invited and contributed.

  9. Comparison of inventory of tritium in various ceramic breeder blankets

    International Nuclear Information System (INIS)

    Nishikawa, M.; Beloglazov, S.; Nakashima, N.; Hashimoto, K.; Enoeda, M.

    2002-01-01

    It has been pointed out by the present authors that it is essential to understand such mass transfer steps as diffusion of tritium in the grain of breeder material, absorption of water vapor into bulk of the grain, and adsorption of water on surface of the grain, together with the isotope exchange reaction between hydrogen in purge gas and tritium on surface of breeder material and the isotope exchange reaction between water vapor in purge gas and tritium on surface, for estimation of the tritium inventory in a uniform ceramic breeder blanket under the steady-state condition. It has been also pointed out by the present authors that the water formation reaction on the surface of ceramic breeder materials at introduction of hydrogen can give effect on behavior of bred tritium and lithium transfer in blanket. The tritium inventory for various ceramic breeder blankets are compared in this study basing on adsorption capacity, absorption capacity, isotope exchange capacity, and isotope exchange reactions on the Li 2 O, LiAlO 2 , Li 2 ZrO 3 , Li 4 SiO 4 and Li 2 TiO 3 surface experimentally obtained by the present authors. Effect of each mass transfer steps on the shape of release curve of bred tritium at change of the operational conditions is also discussed from the observation at out pile experiment in KUR. (orig.)

  10. Mass spectrometry by means of tandem accelerators

    International Nuclear Information System (INIS)

    Tuniz, C.

    1985-01-01

    Mass spectrometry based on an accelerator allows to measure rare cosmogenic isotopes found in natural samples with isotopic abundances up to 10E-15. The XTU Tandem of Legnaro National Laboratories can measure mean heavy isotopes (36Cl, 41Ca, 129I) in applications interesting cosmochronology and Medicine. The TTT-3 Tandem of the Naples University has been modified in view of precision studies of C14 in Archeology, Paleantology and Geology. In this paper a review is made of principles and methodologies and of some applicationy in the framework of the National Program for mass spectrametry research with the aid of accelerators

  11. Accelerator mass spectrometry programme at BARC-TIFR pelletron accelerator

    International Nuclear Information System (INIS)

    Surendran, P.; Shrivastava, A.; Gupta, A.K.; Nair, J.P.; Yadav, M.L.; Gore, J.A.; Sparrow, H.; Bhagwat, P.V.; Kailas, S.

    2006-01-01

    Accelerator based mass spectrometry (ABMs) is an ultra sensitive means of counting individual atoms having sufficiently long half life and available in small amount. The 14 U D Pelletron Accelerator is an ideal machine to carry out ABMs studies with heavy isotopes like 36 Cl and 129 I. Cosmogenic radio isotope 36 Cl is widely being detected using ABMs as it has got applications in ground water research, radioactive waste management, atmospheric 36 Cl transport mechanism studies of Arctic Alpine ice core etc. As a part of the ongoing ABMs programme at 14UD Pelletron Accelerator Facility at Mumbai, a segmented gas detector developed for identification of 36 Cl was tested for performance. Recently a beam chopper required for this measurement has been developed. Further progress made in this programme is discussed in this paper. (author)

  12. Accelerator mass spectrometry.

    Science.gov (United States)

    Hellborg, Ragnar; Skog, Göran

    2008-01-01

    In this overview the technique of accelerator mass spectrometry (AMS) and its use are described. AMS is a highly sensitive method of counting atoms. It is used to detect very low concentrations of natural isotopic abundances (typically in the range between 10(-12) and 10(-16)) of both radionuclides and stable nuclides. The main advantages of AMS compared to conventional radiometric methods are the use of smaller samples (mg and even sub-mg size) and shorter measuring times (less than 1 hr). The equipment used for AMS is almost exclusively based on the electrostatic tandem accelerator, although some of the newest systems are based on a slightly different principle. Dedicated accelerators as well as older "nuclear physics machines" can be found in the 80 or so AMS laboratories in existence today. The most widely used isotope studied with AMS is 14C. Besides radiocarbon dating this isotope is used in climate studies, biomedicine applications and many other fields. More than 100,000 14C samples are measured per year. Other isotopes studied include 10Be, 26Al, 36Cl, 41Ca, 59Ni, 129I, U, and Pu. Although these measurements are important, the number of samples of these other isotopes measured each year is estimated to be less than 10% of the number of 14C samples. Copyright 2008 Wiley Periodicals, Inc.

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

    International Nuclear Information System (INIS)

    Tanaka, Satoru

    1987-01-01

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

  14. 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

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

    Energy Technology Data Exchange (ETDEWEB)

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

    2016-07-01

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

  16. Applications of accelerator mass spectrometry to nuclear physics and astrophysics

    International Nuclear Information System (INIS)

    Guo Zhiyu; Zhang Chuan

    2002-01-01

    As an ultra high sensitive analyzing method, accelerator mass spectrometry is playing an important role in the studies of nuclear physics and astrophysics. The accelerator mass spectrometry (AMS) applications in searching for violation of Pauli exclusion principle and study on supernovae are discussed as examples

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

    Energy Technology Data Exchange (ETDEWEB)

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

    2014-10-15

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

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

    International Nuclear Information System (INIS)

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

    2014-01-01

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

  19. Principle of accelerator mass spectrometry

    International Nuclear Information System (INIS)

    Matsuzaki, Hiroyuki

    2007-01-01

    The principle of accelerator mass spectrometry (AMS) is described mainly on technical aspects: hardware construction of AMS, measurement of isotope ratio, sensitivity of measurement (measuring limit), measuring accuracy, and application of data. The content may be summarized as follows: rare isotope (often long-lived radioactive isotope) can be detected by various use of the ion energy obtained by the acceleration of ions, a measurable isotope ratio is one of rare isotope to abundant isotopes, and a measured value of isotope ratio is uncertainty to true one. Such a fact must be kept in mind on the use of AMS data to application research. (M.H.)

  20. Toxicity and dosimetry of tritium

    International Nuclear Information System (INIS)

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

    1991-01-01

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

  1. The accelerator contains the tritium to discard the spirit decontamination system technique the index sigens estimation

    International Nuclear Information System (INIS)

    Yang Haisu

    2005-10-01

    According to the basic demand of the accelerator application, the main properties and technological constants about building purificatory system of exhaust gas mixed with T (tritium) are analysed and estimated in detail. The system can be operated on the high-flux neutron produce instrument. The vent amount of exhaust gas mixed with T exceeds 4 m 3 /d. The maximal consistency of T approximately is 1 x 10 12 Bq/m 3 , so the parameter of eliminating T should exceed 1 x 10 3 . To adopt the purificatory technique included catalyzing, oxidation, molecular filtration and adsorption is suggested, which is widely used in inland and oversea. In structure, the in and out strobe and a full-automatic intellectual control plus man-control three rank tandem purifying system are adopted to the T density on-line supervisory control devices. (authors)

  2. Observations of the Coronal Mass Ejection with a Complex Acceleration Profile

    Science.gov (United States)

    Reva, A. A.; Kirichenko, A. S.; Ulyanov, A. S.; Kuzin, S. V.

    2017-12-01

    We study the coronal mass ejection (CME) with a complex acceleration profile. The event occurred on 2009 April 23. It had an impulsive acceleration phase, an impulsive deceleration phase, and a second impulsive acceleration phase. During its evolution, the CME showed signatures of different acceleration mechanisms: kink instability, prominence drainage, flare reconnection, and a CME–CME collision. The special feature of the observations is the usage of the TESIS EUV telescope. The instrument could image the solar corona in the Fe 171 Å line up to a distance of 2 {R}ȯ from the center of the Sun. This allows us to trace the CME up to the LASCO/C2 field of view without losing the CME from sight. The onset of the CME was caused by kink instability. The mass drainage occurred after the kink instability. The mass drainage played only an auxiliary role: it decreased the CME mass, which helped to accelerate the CME. The first impulsive acceleration phase was caused by the flare reconnection. We observed the two-ribbon flare and an increase of the soft X-ray flux during the first impulsive acceleration phase. The impulsive deceleration and the second impulsive acceleration phases were caused by the CME–CME collision. The studied event shows that CMEs are complex phenomena that cannot be explained with only one acceleration mechanism. We should seek a combination of different mechanisms that accelerate CMEs at different stages of their evolution.

  3. Analysis of simulated data for the KArlsruhe TRItium Neutrino experiment using Bayesian inference

    DEFF Research Database (Denmark)

    Riis, Anna Sejersen; Hannestad, Steen; Weinheimer, C.

    2011-01-01

    The KATRIN (Karlsruhe Tritium Neutrino) experiment will analyze the tritium β spectrum to determine the mass of the neutrino with a sensitivity of 0.2 eV (90% C.L.). This approach to a measurement of the absolute value of the neutrino mass relies only on the principle of energy conservation and can...

  4. The advantages of orthogonal acceleration in ICP time-of-flight mass spectrometry

    International Nuclear Information System (INIS)

    Gaal, Andrew

    2004-01-01

    The OptiMass 8000 incorporates an orthogonal acceleration time-of-flight mass spectrometer. A general schematic of the instrument is given. The continuous ion beam is chopped by an orthogonal accelerator. A push out pulse supply is coupled to the accelerator for providing repetitive push-out voltages at a frequency of 30 kHz. The ion packets that are sliced out of the beam then travel within the field free space towards the SMARTGATE ion blanker. Orthogonal accelerator parameters are set to enable temporal-spatial focusing at the SMARTGATE ion blanker, so that iso-mass ion packets are resolved in time. Any ion packets of unwanted specie are ejected from the direction of travel by supplying pulsed voltages onto the deflection plates of the SMARTGATE. The ions to be measured are let through SMARTGATE and travel further down the field free space, to enter the ion reflectron. The ion reflectron increases the resolution of the mass spectrometer by means of temporal-energy focussing. After reflection, the ions travel within the field free space towards the discrete-dynode detector. In comparison to other acceleration geometries used in elemental time-of-flight mass spectrometry the OptiMass 8000 orthogonal acceleration geometry ultimately leads to superior resolution. As the energy spread is about 3 orders of magnitude lower in the time-of-flight direction for an oaTOFMS in comparison to an on-axis system, aberration acquired in the initial stages of acceleration are much lower. As a result the orthogonal acceleration scheme provides superior resolution at the first spatial focus point and the detector. The orthogonal acceleration time-of-flight analyzer of the OptiMass 8000 is able to provide resolution of at least 1800 at mass 238. (author)

  5. Tritium storage

    International Nuclear Information System (INIS)

    Hircq, B.

    1990-01-01

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

  6. A GPU Accelerated Spring Mass System for Surgical Simulation

    DEFF Research Database (Denmark)

    Mosegaard, Jesper; Sørensen, Thomas Sangild

    2005-01-01

    There is a growing demand for surgical simulators to dofast and precise calculations of tissue deformation to simulateincreasingly complex morphology in real-time. Unfortunately, evenfast spring-mass based systems have slow convergence rates for largemodels. This paper presents a method to accele...... to accelerate computation of aspring-mass system in order to simulate a complex organ such as theheart. This acceleration is achieved by taking advantage of moderngraphics processing units (GPU)....

  7. A statistical investigation of the mass discrepancy-acceleration relation

    Science.gov (United States)

    Desmond, Harry

    2017-02-01

    We use the mass discrepancy-acceleration relation (the correlation between the ratio of total-to-visible mass and acceleration in galaxies; MDAR) to test the galaxy-halo connection. We analyse the MDAR using a set of 16 statistics that quantify its four most important features: shape, scatter, the presence of a `characteristic acceleration scale', and the correlation of its residuals with other galaxy properties. We construct an empirical framework for the galaxy-halo connection in LCDM to generate predictions for these statistics, starting with conventional correlations (halo abundance matching; AM) and introducing more where required. Comparing to the SPARC data, we find that: (1) the approximate shape of the MDAR is readily reproduced by AM, and there is no evidence that the acceleration at which dark matter becomes negligible has less spread in the data than in AM mocks; (2) even under conservative assumptions, AM significantly overpredicts the scatter in the relation and its normalization at low acceleration, and furthermore positions dark matter too close to galaxies' centres on average; (3) the MDAR affords 2σ evidence for an anticorrelation of galaxy size and Hubble type with halo mass or concentration at fixed stellar mass. Our analysis lays the groundwork for a bottom-up determination of the galaxy-halo connection from relations such as the MDAR, provides concrete statistical tests for specific galaxy formation models, and brings into sharper focus the relative evidence accorded by galaxy kinematics to LCDM and modified gravity alternatives.

  8. Accelerator mass spectrometry for measurement of long-lived radioisotopes.

    Science.gov (United States)

    Elmore, D; Phillips, F M

    1987-05-01

    Particle accelerators, such as those built for research in nuclear physics, can also be used together with magnetic and electrostatic mass analyzers to measure rare isotopes at very low abundance ratios. All molecular ions can be eliminated when accelerated to energies of millions of electron volts. Some atomic isobars can be eliminated with the use of negative ions; others can be separated at high energies by measuring their rate of energy loss in a detector. The long-lived radioisotopes (10)Be, (14)C,(26)A1, 36Cl, and (129)1 can now be measured in small natural samples having isotopic abundances in the range 10(-12) to 10(- 5) and as few as 10(5) atoms. In the past few years, research applications of accelerator mass spectrometry have been concentrated in the earth sciences (climatology, cosmochemistry, environmental chemistry, geochronology, glaciology, hydrology, igneous petrogenesis, minerals exploration, sedimentology, and volcanology), in anthropology and archeology (radiocarbon dating), and in physics (searches for exotic particles and measurement of halflives). In addition, accelerator mass spectrometry may become an important tool for the materials and biological sciences.

  9. Accelerator mass spectrometry in NIPNE

    International Nuclear Information System (INIS)

    Ivascu, M; Marinescu, L.; Dima, R.; Cata-Danil, D.; Petrascu, M.; Popescu, I.; Stan-Sion, C.; Radulescu, M.; Plostinaru, D.

    1997-01-01

    The Accelerator Mass Spectrometry (AMS) is today the method capable to measure the lowest concentration of a particular nuclide in sample materials. The method has applications in environmental physics, medicine, measurements of cosmic-ray or nuclear power plant produced radionuclides in the earth's atmosphere. All over the world, more than 40 charged particles and heavy ion accelerators are performing such analyses concerning the research interest of a huge number of laboratories. The Romanian Institute of Nuclear Physics and Engineering in Bucharest has initiated a construction project for the AMS facility at the FN - Van de Graaff Tandem accelerator. This program benefits of technical and financial assistance provided by IAEA in the frame of the IAEA-TC Project ROM 8014-265C. A general lay-out of the AMS project is presented. The construction work has begun and first tests of the AMS injector will take place between July - September this year. (authors)

  10. 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.)

  11. Tritium calorimeter setup and operation

    CERN Document Server

    Rodgers, D E

    2002-01-01

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

  12. Environmental monitoring for tritium in tritium separation facility

    International Nuclear Information System (INIS)

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

    2001-01-01

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

  13. Environmental monitoring for tritium at tritium separation facility

    International Nuclear Information System (INIS)

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

    2001-01-01

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

  14. Non-intrusive measurement of tritium activity in waste drums by modelling a 3He leak quantified by mass spectrometry

    International Nuclear Information System (INIS)

    Demange, D.

    2002-01-01

    This study deals with a new method that makes it possible to measure very low tritium quantities inside radioactive waste drums. This indirect method is based on measuring the decaying product, 3 He, and requires a study of its behaviour inside the drum. Our model considers 3 He as totally free and its leak through the polymeric joint of the drum as two distinct phenomena: permeation and laminar flow. The numerical simulations show that a pseudo-stationary state takes place. Thus, the 3 He leak corresponds to the tritium activity inside the drum but it appears, however, that the leak peaks when the atmospheric pressure variations induce an overpressure in the drum. Nevertheless, the confinement of a drum in a tight chamber makes it possible to quantify the 3 He leak. This is a non-intrusive measurement of its activity, which was experimentally checked by using reduced models, representing the drum and its confinement chamber. The drum's confinement was optimised to obtain a reproducible 3 He leak measurement. The gaseous samples taken from the chamber were purified using selective adsorption onto activated charcoals at 77 K to remove the tritium and pre-concentrate the 3 He. The samples were measured using a leak detector mass spectrometer. The adaptation of the signal acquisition and the optimisation of the analysis parameters made it possible to reach the stability of the external calibrations using standard gases with a 3 He detection limit of 0.05 ppb. Repeated confinement of the reference drums demonstrated the accuracy of this method. The uncertainty of this non-intrusive measurement of the tritium activity in 200-liter drums is 15% and the detection limit is about 1 GBq after a 24 h confinement. These results led to the definition of an automated tool able to systematically measure the tritium activity of all storage waste drums. (authors)

  15. 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)

  16. Operating experience with TFTR's Tritium Storage and Delivery System

    International Nuclear Information System (INIS)

    Voorhees, D.R.

    1995-01-01

    The Tritium Storage and Delivery System (TSDS) at TFTR was fabricated at Monsanto Mound Lab in the late 1970's and delivered to PPPL in the early 1980's. Commissioning progressed slowly and was finally completed in 1992 following a series of Preoperational tests and Integrated Systems tests. Those tests included thorough leak testing of glove boxes and process piping, electrical interlocks and controls, instrumentation calibrations, volume determinations and verification of uranium bed capacity. The system accepted tritium in dilute form in May of 1993 and began serious usage of pure tritium in November 1993. As the throughput of high purity tritium increased, shortcomings of the system became evident and extensive repairs were implemented. System leakage and material compatibility were the primary causes of the problems. To date, the system has received, stored and delivered over 500 kCi of tritium and is performing very well. The dedicated quadrupole mass spectrometer and beta scintillator system has been analyzing tritium bearing and pure gas streams for over 3 years with minimal downtime

  17. 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)

  18. A New Accelerator-Based Mass Spectrometry.

    Science.gov (United States)

    Gove, H. E.

    1983-01-01

    Tandem electrostatic accelerators produce beams of positive ions which are used to penetrate atomic nuclei in a target, inducing nuclear reactions whose study elucidates varied properties of the nucleus. Uses of the system, which acts like a mass spectrometer, are discussed. These include radiocarbon dating measurements. (JN)

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

    International Nuclear Information System (INIS)

    1995-10-01

    Tritium, a radioactive gas used in all of the Nation's nuclear weapons, has a short half-life and must be replaced periodically in order for the weapon to operate as designed. Currently, there is no capability to produce the required amounts of tritium within the Nuclear Weapons Complex. The PEIS for Tritium Supply and Recycling evaluates the alternatives for the siting, construction, and operation of tritium supply and recycling facilities at each of five candidate sites: the Idaho National Engineering Laboratory, the Nevada Test Site, the Oak Ridge Reservation, the Pantex Plant, and the Savannah River Site. Alternatives for new tritium supply and recycling facilities consist of four different tritium supply technologies: Heavy Water Reactor, Modular High Temperature Gas-Cooled Reactor, Advanced Light Water Reactor, and Accelerator Production of Tritium. The PEIS also evaluates the impacts of the DOE purchase of an existing operating or partially completed commercial light water reactor or the DOE purchase of irradiation services contracted from commercial power reactors. Additionally, the PEIS includes an analysis of multipurpose reactors that would produce tritium, dispose of plutonium, and produce electricity. Evaluation of impacts on land resources, site infrastructure, air quality and acoustics, water resources, geology and soils, biotic resources, cultural and paleontological resources, socioeconomics, radiological and hazardous chemical impacts during normal operation and accidents to workers and the public, waste management, and intersite transport are included in the assessment

  20. 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.)

  1. The future of the accelerator mass spectrometry of rare long-lived radioactive isotopes

    International Nuclear Information System (INIS)

    Litherland, A.E.

    1990-01-01

    Accelerators, originally designed for nuclear physics, can be added to mass spectrometric apparatus to increase the sensitivity so that isotope ratios in the range 10 -12 to 10 -15 can be measured routinely. This significant improvement of high-sensitivity mass spectrometry has been called Accelerator Mass Spectrometry. The present article addresses the basic principles of accelerator mass spectrometry and some recent applications which show its versatility. In particular, it is noted that accelerator mass spectrometry could play an increasing role in the measurement of the levels of long lived radioactivities in the environment, including the actinides, which result from human activities such as the use of nuclear power. To fulfill this promise, continued research and development is necessary to provide ion sources, various types of heavy ion accelerators and peripheral magnetic and electric analysers. (N.K.)

  2. 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)

  3. 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)

  4. Tritium Management In HCLL-PPCS Model AB Blanket

    International Nuclear Information System (INIS)

    Ricapito, I.; Aiello, A.; Benamati, G.; Utili, M.; Ciampichetti, A.; Zucchetti, M.

    2006-01-01

    One the main issues in the HCLL blanket development for a prototype fusion reactor is the technical feasibility of the bred tritium processing system. The basis of such concern lies in the very low tritium-Pb17Li Sieverts' constant, as measured by different scientists in the past years. In the PPCS reactor 650 g/d of tritium must be generated in the breeding blanket while less than 1 g/y of tritium has to be released to the environment through the secondary cooling circuit. As a consequence, CPS (Coolant Purification System) plays a fundamental role because it has to keep at an acceptable level the tritium partial pressure in the primary HCS (Helium Cooling Circuit) limiting, therefore, the tritium environmental release through leakage and permeation into the secondary cooling circuit. On the other hand, the He mass flow-rate to be processed by CPS is linear with the tritium permeation rate from the breeder into HCS. Therefore, with the above mentioned low Sieverts' constant values and the consequent high tritium partial pressure in the liquid metal, the possibility to keep acceptable the CPS capacity depends on a highly efficient and stable performance of tritium permeation barriers, to be applied not only on the blanket cooling plates but also on the steam generator walls. However, the experimental results on the tritium permeation barriers under relevant operative conditions were so far quite disappointing. The new data on the Sieverts' constant achieved at ENEA CR Brasimone, one order of magnitude higher than those founding the past, have a big impact in relaxing the above mentioned requirements for the tritium management in PPCS model AB reactor. Besides presenting and discussing these recent experimental results, an updated assessment of the tritium permeation rate from the liquid breeder into HCS through the cooling plates and from HCS into the environment through the steam generators is given in this paper. The consequent new constraints in terms of tritium

  5. The measurement of tritium in Canadian food items

    International Nuclear Information System (INIS)

    Brown, R.M.

    1995-03-01

    Food items locally grown near Perth, Ontario and grocery store produce and locally grown items from the Pickering-Ajax area in the vicinity of the Pickering Nuclear Generating Station (PNGS) have been analyzed for free water tritium (HTO) and organically bound tritium (OBT). The technique of measuring 3 He ingrowth in samples by mass spectrometry has been used because of its sensitivity and freedom from opportunity for contamination during processing and measurement. Concentrations observed at each site were of the order expected on the basis of known levels of tritium in the local atmosphere and precipitation. There was considerable variation between different materials and limited correlation between materials of a single type. (author). 10 refs., 8 tabs., 4 figs

  6. Cold fusion produces more tritium than neutrons

    International Nuclear Information System (INIS)

    Rajagopalan, S.R.

    1989-01-01

    The results of the major cold fusion experiments performed in various laboratories of the world and attempts to explain them are reviewed in brief. Particular reference is made to the experiments carried out in the Bhabha Atomic Research Centre (BARC), Bombay. In BARC experiments, it is found that tritium is the primary product of cold fusion. Author has put forward two hypothetical pictures of D-D fusion. (1) When a metal like Pd or Ti is loaded with D 2 , a crack forms. Propogation of such a crack accelerates deuterons which bombard Pd D 2 /D held by Pd or Ti leading to neutron capture or tritium formation with the release of protons and energy. The released protons might transfer its energy to some other deuteron and a chain reaction is started. This chain reaction terminates when a substantial portion of D in the crack tip is transmuted. This picture explains fusion reaction bursts and the random distribution of reaction sites, but does not explain neutron emission. (2) The deuterons accelerated by a propogating crack may hit a Pd/Ti nucleus instead of a deuterium nucleus and may transmute Pd/Ti. (M.G.B.). 18 refs

  7. Developing an environmental compliance program for accelerator production of tritium

    International Nuclear Information System (INIS)

    Reynolds, R.W.; Roberts, J.S.; Dyer, K.W.; Shedrow, C.B.; Sheetz, S.O.; England, J.L.

    1998-01-01

    This paper addresses the development of an environmental program for a large proposed federal project currently in the preliminary design phase, namely, the accelerator production of tritium (APT) for the US Department of Energy (DOE). This project is complicated not only by its size ($3.5 to $4.5 billion) but also by its technical complexity and one-of-a-kind nature. This is further complicated by the fact that government projects are driven by budgets subject to public pressures and annual Congressional fiscal considerations, whereas private companies are driven by profits. The measure of success for a federal project such as the APT is based on level of public support, not profits. Finally, there are not too many equivalent environmental programs that could be used as models, and benchmarking is nearly impossible. Forming an environmental program during the conceptual design phase of this large federal project included the formation of a core environmental working group (EWG). The group has membership from all major project organizations with a charter formally recognized by the project director. The envelope for traditional environmental work for the APT project has been stretched to include teaming with management in the establishment of project goals and direction. The APT EWG was set up organizationally to include several subgroups or teams that do the real work of assessing, establishing the regulatory framework, and then developing a compliance program. Setting aside the organizational difficulties of selecting the right team leads and members, each team was tasked with developing a charter, plan, and schedule. Since then, each team has developed an appropriate level of supporting documentation to address its particular issues and requirements

  8. Development of advanced tritium breeding material with added lithium for ITER-TBM

    Energy Technology Data Exchange (ETDEWEB)

    Hoshino, Tsuyoshi, E-mail: hoshino.tsuyoshi@jaea.go.jp [Blanket Irradiation and Analysis Group, Fusion Research and Development Directorate, Japan Atomic Energy Agency, 4002, Narita-cho, Oarai-machi, Higashi Ibaraki-gun, Ibaraki 311-1393 (Japan); Kato, Kenichi; Natori, Yuri; Oikawa, Fumiaki; Nakano, Natsuko; Nakamura, Mutsumi [Kaken, Co. Ltd., 1044, Hori, Mito-city, Ibaraki 310-0903 (Japan); Sasaki, Kazuya [Institute of Engineering Innovation and Department of Nuclear Engineering and Management School of Engineering, University of Tokyo, 2-11-16 Yayoi, Bunkyo-ku, Tokyo 113-8656 (Japan); Suzuki, Akihiro [Nuclear Professional School, School of Engineering, University of Tokyo, 2-22 Shirakata-Shirane, Ibaraki 319-1188 (Japan); Terai, Takayuki [Institute of Engineering Innovation and Department of Nuclear Engineering and Management School of Engineering, University of Tokyo, 2-11-16 Yayoi, Bunkyo-ku, Tokyo 113-8656 (Japan); Tatenuma, Katsuyoshi [Kaken, Co. Ltd., 1044, Hori, Mito-city, Ibaraki 310-0903 (Japan)

    2011-10-01

    Lithium titanate (Li{sub 2}TiO{sub 3}) is one of the most promising candidates among tritium breeding materials because of its good tritium release characteristics. However, the mass of Li{sub 2}TiO{sub 3} decreased with time in a hydrogen atmosphere by the reduction of Ti and Li evaporation. In order to prevent the mass decrease at high temperatures, advanced tritium breeding material with added Li (Li{sub 2+x}TiO{sub 3+y}) should be developed. For this purpose, an advanced Li{sub 2}TiO{sub 3} with added Li was synthesized from proportionally mixed LiOH.H{sub 2}O and H{sub 2}TiO{sub 3} with a Li/Ti ratio of 2.2. The results of X-ray diffraction measurement showed that this advanced tritium breeding material existed as the non-stoichiometric compound Li{sub 2+x}TiO{sub 3+y}. The desired molar ratio of Li/Ti was achieved by appropriate mixing of LiOH.H{sub 2}O and H{sub 2}TiO{sub 3}. Therefore, synthesis by mixing LiOH.H{sub 2}O and H{sub 2}TiO{sub 3} is a promising mass production method for the advanced tritium breeding material with added Li for the test blanket module of ITER.

  9. 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)

  10. Radiocarbon accelerator mass spectrometry: background and contamination

    International Nuclear Information System (INIS)

    Beukens, R.P.

    1993-01-01

    Since the advent of radiocarbon accelerator mass spectrometry (AMS) many studies have been conducted to understand the background from mass spectrometric processes and the origins of contamination associated with the ion source and sample preparation. By studying the individual contributions a better understanding of these processes has been obtained and it has been demonstrated that it is possible to date samples reliably up to 60 000 BP. (orig.)

  11. Observation of the movement of the precipitation by using tritium tracer

    International Nuclear Information System (INIS)

    Jiao, Yurong; Ishida, Sayuri; Takada, Kayoko; Imaizumi, Hiroshi; Kano, Naoki; Saito, Masaaki

    2011-01-01

    Tracer techniques have proven to be one of the most powerful tools to characterize the movement of air mass and pollutant transport in hydrological systems. In order to clarify the behavior of low-level tritium in the rain water, we have employed the measuring method of tritium applying a distillation process and an electrolytic enrichment process. The activity of tritium (T specific activity) in the obtained water was measured by liquid scintillation counter. This procedure was applied to bulk precipitation, imitative ground infiltrated precipitation and short term precipitation collected in Niigata City. Moreover, we investigated the concentrations of cations (Na + , K + , Ca 2+ , and Mg 2+ ) in the precipitation to associate with air mass transport patterns arriving at the place. From the above mentioned, next matters have been clarified: (1) T specific activity in precipitation was found to have a strong dependence on location and season. (2) The chemical components in precipitation during typhoon have notable character of marine air mass. (3) Associated ions in monthly precipitation showed seasonal variation, in fact, the seasonal variation of Ca 2+ and tritium were very similar. (4) Backward trajectory analysis method is useful for the analysis of the behavior of T specific activity and several ions in short-term precipitation. (author)

  12. Tritium calorimeter setup and operation

    International Nuclear Information System (INIS)

    Rodgers, David E.

    2002-01-01

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

  13. 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.))

  14. 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

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

    International Nuclear Information System (INIS)

    1995-10-01

    Tritium, a radioactive gas used in all of the Nation's nuclear weapons, has a short half-life and must be replaced periodically in order for the weapon to operate as designed. Currently, there is no capability to produce the required amounts of tritium within the Nuclear Weapons Complex. The PEIS for Tritium Supply and Recycling evaluates the alternatives for the siting, construction, and operation of tritium supply and recycling facilities at each of five candidate sites: the Idaho National Engineering Laboratory, the Nevada Test Site, the Oak Ridge Reservation, the Pantex Plant, and the Savannah River Site. Alternatives for new tritium supply and recycling facilities consist of four different tritium supply technologies: Heavy Water Reactor, Modular High Temperature Gas-Cooled Reactor, Advanced Light Water Reactor, and Accelerator Production of Tritium. The PEIS also evaluates the impacts of the DOE purchase of an existing operating or partially completed commercial light water reactor or the DOE purchase of irradiation services contracted from commercial power reactors. Additionally, the PEIS includes an analysis of multipurpose reactors that would produce tritium, dispose of plutonium, and produce electricity. Evaluation of impacts on land resources, site infrastructure, air quality and acoustics, water resources, geology and soils, biotic resources, cultural and paleontological resources, socioeconomics, radiological and hazardous chemical impacts during normal operation and accidents to workers and the public, waste management, and intersite transport are included in the assessment. 550 refs

  16. 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.)

  17. Use of Helium-3 and Tritium tracers in oceanography

    International Nuclear Information System (INIS)

    Andrie, Chantal

    1987-01-01

    As tritium considered as a transient tracer has become one of the most promising tool for the study of oceanic circulation and of the ocean capacity to absorb anthropogenic carbon, and as the simultaneous use of its radioactive descendant, Helium-3, brings an additional information (together, these tracers build up a clock in the study of water masses), and as all helium-3 and tritium measurements are made by mass spectroscopy, this research thesis addresses the analytical process, the detection limit, and the method reproducibility associated with this use of both tracers. The author reports and discusses helium-3 data obtained during a measurement campaign which allowed the localisation of an active source and the evidence of an intermediate back current, and tritium data obtained during another measurement campaign which allowed the description of the high time variability of convection processes, and an assessment of water renewal delays and of some deep water circulations. He also reports and discusses the simultaneous use of helium-3 data and tritium data to localize areas where convection processes occur. A theoretical approach to this simultaneous use is proposed which uses a mixing model which distinguishes the venting transit time. Measurement campaigns were performed in Red Sea, western Mediterranean Sea, and north-eastern Atlantic Ocean [fr

  18. Transfer of tritium to prenatal and neonatal rats from their mothers exposed to tritiated compounds

    Energy Technology Data Exchange (ETDEWEB)

    Takeda, H.; Nishimura, Y.; Inaba, J. (National Inst. of Radiological Sciences, Chiba (Japan))

    1994-01-01

    The transfer of tritium through the placenta or milk was investigated to estimate the radiation dose to the fetus and newborn. Female rats at gestational stages or after delivery were exposed to tritium in the form of water, thymidine and lysine by a single oral administration and radioactivity in tissues including conceptuses (placenta, fetal membrane and fetus) and in the newborn was determined at various times after administration. In all cases of the investigated triated compounds, there was no significant difference between the tritium concentration in the fetus and that in the maternal tissues, suggesting that the placenta has no effect in preventing or accelerating the placental transfer of tritium. The time course of tritium concentration and tritium content in the fetus and newborn were, however, dependent on the chemical form of tritium and on the prenatal or neonatal stages at the time of ingestion. In general, the tritium concentration and tritium content after the ingestion of [sup 3]H-lysine were higher than that after the ingestion of tritiated water or [sup 3]H-thymidine. The result of dose estimation showed that [sup 3]H-lysine gave higher prenatal and neonatal doses than tritiated water or [sup 3]H-thymidine by a factor of 1.5 to 6.0. (author).

  19. Safe handling of tritium

    International Nuclear Information System (INIS)

    1991-01-01

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

  20. Control of the tritium path in process heat HTR's

    International Nuclear Information System (INIS)

    Kirch, N.; Scheidler, G.

    1985-01-01

    Nuclear Process Heat plant converting fossil fuels into liquid or gaseous secondary energy carriers generate tritium by several nuclear reactions. Control of the tritium path through the walls of the heat exchanger is highly important to meet regulatory requirements on the acceptable contamination in the product gas or liquid. Therefore, significant effort in the project 'Prototypanlage Nukleare Prozesswaerme' was put not only into generating a data base, but also into means of reducing tritium generation and permeation. Clean graphites with lithium impurities in the ppb level provide a low tritium source term. Realistic modeling of graphite retention and special helium purification systems are essentials. The main barrier to tritium permeation are heat exchanger walls requiring detailed characterization of in-situ surface layers. Studies to optimize the water/steam mass flow in the conversion process offer possibilities for further tritium retention. Progress can be demonstrated as follows: In 1980, between 2 and 8 Bq tritium per gram of product were predicted based on available data and even higher concentrations during startup. However, present day validated code predictions are below required 0.5 Bq/g equilibrium concentration level. During transients - particularly startup - this limit cannot be guaranteed as yet, but further retention potential is being offered by tritium gettering or filtering. An expected increase of the German regulatory requirement to 5 Bq/g will easily be met by present plant design under all operational conditions. (author)

  1. Tritium isotopic exchange in air detritiation dryers

    International Nuclear Information System (INIS)

    Everatt, A.E.; Johnson, R.E.; Senohrabek, J.A.; Shultz, C.M.

    1989-02-01

    Isotopic exchange between tritiated and non-tritiated water species in a molecular sieve bed has been demonstrated. At high humidities (+6 degrees Celsius dew point) the rate of tritium isotopic exchange in a 2.4 L molecular sieve bed has been demonstrated to be at least 50% of published exchange rates. In an industrial-sized air detritiation dryer, utilizing the pretreatment technique of H 2 O steam washing to elute the residual tritium, a DF of 12 600 has been demonstrated when operating at an inlet vapor tritium concentration of 14 Ci/kg and at inlet and outlet dew points of 4.8 and -54 degrees Celsius, respectively. In the NPD dryer bed studied, which was not optimally designed for full benefit from isotopic exchange, at least one order of magnitude in additional detritiation is attributed to isotopic exchange in the unsaturated zone. The technique of eluting the residual tritium from an industrial sized bed by H 2 O washing at high temperature, high humidity and low bed loading has been demonstrated to be a fast and effective way of removing tritium from a molecular sieve bed during regeneration. The isotopic exchange model accurately predicted the exchange between tritiated and non-tritiated water species in a molecular sieve bed where there is no net adsorption or desorption. The model's prediction of the tritium breakthrough trend observed in the NPD tests was poor; however, a forced fit can be achieved if the exchange rates in the MTZ and the unsaturated zone are manipulated. More experiments are needed to determine the relative rates of tritium exchange in the saturated, mass transfer, and unsaturated zones of a dryer bed

  2. 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.)

  3. 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

  4. 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

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

    Energy Technology Data Exchange (ETDEWEB)

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

    2015-11-15

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

  6. Tritium monitoring techniques

    International Nuclear Information System (INIS)

    DeVore, J.R.; Buckner, M.A.

    1996-05-01

    As part of their operations, the U.S. Navy is required to store or maintain operational nuclear weapons on ships and at shore facilities. Since these weapons contain tritium, there are safety implications relevant to the exposure of personnel to tritium. This is particularly important for shipboard operations since these types of environments can make low-level tritium detection difficult. Some of these ships have closed systems, which can result in exposure to tritium at levels that are below normally acceptable levels but could still cause radiation doses that are higher than necessary or could hamper ship operations. This report describes the state of the art in commercial tritium detection and monitoring and recommends approaches for low-level tritium monitoring in these environments

  7. OBT measurement of vegetation by mass spectrometry and radiometry

    International Nuclear Information System (INIS)

    Tamari, T.; Kakiuchi, H.; Momoshima, N.; Sugihara, S.; Baglan, N.; Uda, T.

    2011-01-01

    We carried out OBT (organically bound tritium) measurement by two different methods those are radiometry and mass spectrometry and compared the applicability of these methods for environmental tritium analysis. The dried grass sample was used for the experiments. To eliminate the exchangeable OBT, the sample was washed with tritium free water before analysis. Three times washing reduced the tritium activity in the labile sites below the detectable level. In radiometry the sample was combusted to convert the OBT as well as other hydrogen isotopes to. water and tritium activity in the water was measured by liquid scintillation counting (LSC). In mass spectrometry, the sample was kept in a glass container and 3 He produced by tritium decay was measured by mass spectrometry. The results were in good agreement suggesting applicability of these methods for environmental tritium analysis. The mass spectrometry is more suitable for environmental tritium research because of a lower detection limit than that of the LSC. (authors)

  8. 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

  9. Status of the Los Alamos tritium beta decay experiment

    International Nuclear Information System (INIS)

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

    1989-01-01

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

  10. 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

  11. Mixing and mass transfer in bubble extractor: its application to tritium extraction from 17Li83Pb

    International Nuclear Information System (INIS)

    Baratti, R.; Polcaro, A.M.; Ricci, P.F.; Viola, A.; Pierini, G.

    1986-01-01

    The tritium extraction from the liquid alloy 17Li83Pb has been examined taking into consideration the equations related to the design of bubble extractors in order to verify which are the highest tritium recovery efficiencies which can be realized so as to minimize the tritium permeation into the water of the cooling system. For the tritium desorption from alloy, flowing countercurrent to a helium stream in a bubble extractor, the axial dispersion in liquid and gaseous phase and the effect of gas phase expansion caused by reduced hydrostatic head in the extractor are taken into account. Taking into consideration some NET technical specifications, such as the alloy volume in the blanket of 65 m 3 and the tritium generation rate of 78 g.d -1 , the results are presented and discussed

  12. 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)

  13. 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

  14. 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

  15. 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

  16. Determination of {sup 135}Cs by accelerator mass spectrometry

    Energy Technology Data Exchange (ETDEWEB)

    MacDonald, C.M.; Charles, C.R.J. [Andre. E. Lalonde AMS Laboratory, University of Ottawa, 150 Louis Pasteur, Ottawa, ON K1N 6N5 (Canada); Department of Earth Sciences, University of Ottawa, 150 Louis Pasteur, Ottawa, ON K1N 6N5 (Canada); Zhao, X.-L.; Kieser, W.E. [Andre. E. Lalonde AMS Laboratory, University of Ottawa, 150 Louis Pasteur, Ottawa, ON K1N 6N5 (Canada); Department of Physics, University of Ottawa, 150 Louis Pasteur, Ottawa, ON K1N 6N5 (Canada); Cornett, R.J. [Andre. E. Lalonde AMS Laboratory, University of Ottawa, 150 Louis Pasteur, Ottawa, ON K1N 6N5 (Canada); Department of Earth Sciences, University of Ottawa, 150 Louis Pasteur, Ottawa, ON K1N 6N5 (Canada); Litherland, A.E. [IsoTrace Laboratory, University of Toronto, 60 St. George St., Toronto, ON M5S 1A7 (Canada)

    2015-10-15

    The ratio of anthropogenic {sup 135}Cs and {sup 137}Cs isotopes is characteristic of a uranium fission source. This research evaluates the technique of isotope dilution (yield tracing) for the purpose of quantifying {sup 135}Cs by accelerator mass spectrometry with on-line isobar separation. Interferences from Ba, Zn{sub 2}, and isotopes of equal mass to charge ratios were successfully suppressed. However, some sample crosstalk from source contamination remains. The transmission and di-fluoride ionization efficiencies of Cs isotopes were found to be 8 × 10{sup −3} and 1.7 × 10{sup −7} respectively. This quantification of {sup 135}Cs using yield tracing by accelerator mass spectrometry shows promise for future environmental sample analysis once the issues of sample crosstalk and low efficiency can be resolved.

  17. Confirmatory experiments for the United States Department of Energy Accelerator Production of Tritium Program: Neutron, triton and radionuclide production by thick targets of lead and tungsten bombarded by 800 MeV protons

    International Nuclear Information System (INIS)

    Lisowski, P.W.; Cappiello, M.; Ullmann, J.L.; Gavron, A.; King, J.D.; Laird, R.; Mayo, D.; Waters, L.; Zoeller, C.; Staples, P.

    1994-01-01

    Neutron and Triton Production by 800 MeV Protons: The experiments presented in this report were performed in support of the Accelerator Production of Tritium (APT) project at the Los Alamos Weapons Neutron Research (WNR) facility in order to provide data to benchmark and validate physics simulations used in the APT target/blanket design. An experimental apparatus was built that incorporated many of the features of the neutron source region of the 3 He target/blanket. Those features included a tungsten neutron source, flux traps, neutron moderator, lead backstop, lead multiplying annulus, neutron absorbing blanket and a combination neutron de-coupler and tritium producing gas ( 3 He). The experiments were performed in two separate proton irradiations each with approximately 100 nA-hr of 800 MeV protons. The first irradiation was made with a small neutron moderating blanket, allowing the authors to measure tritium production in the 3 He gas by sampling, and counting the amount of tritium. The second irradiation was performed with a large neutron moderating blanket (light water with a 1% manganese sulfate solution) that allowed them to measure both the tritium production in the central region and the total neutron production. The authors did this by sampling and counting the tritium produced and by measuring the activation of the manganese solution. Results of the three tritium production measurements show large disagreements with each other and therefore with the values predicted using the LAHET-MCNP code system. The source of the discrepancies may lie with the sampling system or adsorption on the tungsten surfaces. The authors discuss tests that may resolve that issue. The data for the total neutron production measurement is much more consistent. Those results show excellent agreement between calculation and experiment

  18. Theoretical study of β-decay of a negative tritium ion

    International Nuclear Information System (INIS)

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

    1997-01-01

    A calculation of the probability of the main β-decay channel of a negative tritium ion is described as one of the processes that can affect the β-spectrum of a tritium source near the end point. The appropriate energy parameters have been calculated. This process should be taken into account in interpreting measured β-spectra near the end point in connection with determining the neutrino rest mass

  19. 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.

  20. Tritium production potential of beam research and magnetic fusion program technologies

    International Nuclear Information System (INIS)

    Lee, J.D.

    1989-03-01

    Regular replenishment of tritium in the nuclear weapons stockpile is essential to maintain our nuclear deterrent. Nuclear reactor facilities presently used for the production of tritium are aging, and their operation is being curtailed awaiting the repairs and upgrades needed to meet modern standards of safety and environment. To provide improved capability in the future, DOE plans to construct a new production reactor. Alternatives to nuclear reactor methods for the production of tritium, mainly electrically-driven accelerator or fusion systems, have been proposed many times in the past. Given the critical national security implications of maintaining adequate tritium production facilities, it is clearly worthwhile for political decision-makers to have a clear and accurate picture of the technical options that could be made available at various points in the future. The goal of this white paper is to summarize available technical information on a set of non-nuclear-reactor options for tritium production with a minimum of advocacy for any one system of implicit assumptions about politically desirable attributes. Indeed, these various options differ considerably in aspects such as the maturity of the technology, the development cost and timescales required, and the capital and operating costs of a typical ''optimized'' facility

  1. Accelerator mass spectrometry programme at BARC-TIFR pelletron accelerator. PD-1-2

    International Nuclear Information System (INIS)

    Bhagwat, P.V.

    2007-01-01

    Accelerator mass spectrometry (AMS) is an ultra sensitive means of counting individual atoms having sufficiently long half-life and available in small amount. The 14 UD Pelletron Accelerator is an ideal machine to carry out AMS studies with heavy isotopes like 36 Cl and 129 I. Cosmogenic radioisotope 36 Cl is widely being detected using AMS as it has got applications in ground water research, radioactive waste management, atmospheric 36 Cl transport mechanism studies of Arctic Alpine ice core etc . The AMS programme at the 14 UD Mumbai Pelletron Accelerator has taken off with the installation of the state of the art Terminal Potential Stabilizer setup and operation of the accelerator in Generating Volt Meter (GVM) mode. Feasibility studies have been carried out for detection/identification of 14 C from a charcoal sample and 3 He in natural Helium. As the primary interest of AMS programme at Mumbai Pelletron Accelerator is related to the cosmogenic nuclei, 36 Cl and 129 I, a segmented gas detector developed for identification of 36 Cl was tested for performance. Recently a beam chopper required for this measurement has also been developed

  2. 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

  3. LINAC for ADS application - accelerator technologies

    International Nuclear Information System (INIS)

    Garnett, Robert W.; Sheffreld, Richard L.

    2009-01-01

    Sifnificant high-current, high-intensity accelerator research and development have been done in the recent past in the US, centered primarily at Los Alamos National Laboratory. These efforts have included designs for the Accelerator Production of Tritium Project, Accelerator Transmutation of Waste, and Accelerator Driven Systems, as well as many others. This past work and some specific design principles that were developed to optimie linac designs for ADS and other high-intensity applications will be discussed briefly.

  4. 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

  5. Progress report on the Los Alamos tritium beta decay experiment

    International Nuclear Information System (INIS)

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

    1988-01-01

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

  6. 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

  7. 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

  8. 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

  9. U.S. advanced accelerator applications program: plans to develop and test waste transmutation technologies

    International Nuclear Information System (INIS)

    Van Tuyle, G.; Bennett, D.; Arthur, E.; Cappiello, M.; Finck, P.; Hill, D.; Herczeg, J.; Goldner, F.

    2001-01-01

    The primary mission of the U.S. Advanced Accelerator Applications (AAA) Program is to establish a national nuclear technology research capability that can demonstrate accelerator-based transmutation of waste and conduct transmutation research while at the same time providing a capability for the production of tritium if required. The AAA Program was created during fiscal year 2001 from the Accelerator Transmutation of Waste (ATW) Program and the Accelerator Production of Tritium (APT) Project. This paper describes the new AAA Program, as well as its two major components: development and testing of waste transmutation technologies and construction of an integrated accelerator-driven test facility (ADTF). (author)

  10. 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

  11. 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

  12. 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

  13. 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

  14. 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)

  15. Absolute measurement of a tritium standard

    International Nuclear Information System (INIS)

    Hadzisehovic, M.; Mocilnik, I.; Buraei, K.; Pongrac, S.; Milojevic, A.

    1978-01-01

    For the determination of a tritium absolute activity standard, a method of internal gas counting has been used. The procedure involves water reduction by uranium and zinc further the measurement of the absolute disintegration rate of tritium per unit of the effective volume of the counter by a compensation method. Criteria for the choice of methods and procedures concerning the determination and measurement of gaseous 3 H yield, parameters of gaseous hydrogen, sample mass of HTO and the absolute disintegration rate of tritium are discussed. In order to obtain gaseous sources of 3 H (and 2 H), the same reversible chemical reaction was used, namely, the water - uranium hydride - hydrogen system. This reaction was proved to be quantitative above 500 deg C by measuring the yield of the gas obtained and the absolute activity of an HTO standard. A brief description of the measuring apparatus is given, as well as a critical discussion of the brass counter quality and the possibility of obtaining equal working conditions at the counter ends. (T.G.)

  16. 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

  17. 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

  18. 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

  19. A tritium target system for μCF

    International Nuclear Information System (INIS)

    Zmeskal, J.; Ackerbauer, P.; Durham, W.B.; Heard, H.C.; Neumann, W.; Bossy, H.

    1990-12-01

    An apparatus has been constructed for the safe handling of tritium as part of a series of muon-catalyzed fusion experiments. The equipment was designed to handle 100 kCi of tritium. The main parts of this system are the oil-free high vacuum and transfer system, and the quadrupole mass analyzer for a direct determination of the target content. The system was used successfully for five continuous periods of operation of over one month each. A new target system was constructed at Lawrence Livermore National Laboratory (LLNL) for ultimate use at Paul Scherrer Institute (PSI) to investigate the high temperature and high pressure region. 9 refs., 4 figs

  20. Continuous-flow accelerator mass spectrometry for radiocarbon analysis

    International Nuclear Information System (INIS)

    Wills, J.S.C.; Han, B.X.; Von Reden, K.F.; Schneider, R.J.; Roberts, M.L.

    2006-01-01

    Accelerator Mass Spectrometry (AMS) is a widely used technique for radiocarbon dating of archaeological or environmental samples that are very small or very old (up to 50,000 years before present). Because of the method's extreme sensitivity, AMS can also serve as an environmental tracer and supplements conventional nuclear counting techniques for monitoring 14 C emissions from operating nuclear power plants and waste repositories. The utility of present AMS systems is limited by the complex sample preparation process required. Carbon from combusted artefacts must be incorporated into a solid metallic target from which a negative ion beam is produced and accelerated to MeV energies by an accelerator for subsequent analysis. This paper will describe a novel technique being developed by the National Ocean Sciences Accelerator Mass Spectrometry (NOSAMS) Laboratory at the Woods Hole Oceanographic Institution for the production of negative carbon ion beams directly from a continuously flowing sample gas stream, eliminating the requirement for a solid target. A key component of the new technique is a microwave-driven, gaseous-feed ion source originally developed at Chalk River Laboratories for the very different requirements of a high current proton linear accelerator. A version of this ion source is now being adapted to serve as an injector for a dedicated AMS accelerator facility at NOSAMS. The paper begins with a review of the fundamentals of radiocarbon dating. Experiments carried out at NOSAMS with a prototype of the microwave ion source are described, including measurements of sample utilization efficiency and sample 'memory' effect. A new version of the microwave ion source, optimized for AMS, is also described. The report concludes with some predictions of new research opportunities that will become accessible to the technique of continuous-flow AMS. (author)

  1. Continuous-flow accelerator mass spectrometry for radiocarbon analysis

    International Nuclear Information System (INIS)

    Wills, J.S.C.; Han, B.X.; Von Reden, K.F.; Schneider, R.J.; Roberts, M.L.

    2006-05-01

    Accelerator Mass Spectrometry (AMS) is a widely used technique for radiocarbon dating of archaeological or environmental samples that are very small or very old (up to 50,000 years before present). Because of the method's extreme sensitivity, AMS can also serve as an environmental tracer and supplements conventional nuclear counting techniques for monitoring 14 C emissions from operating nuclear power plants and waste repositories. The utility of present AMS systems is limited by the complex sample preparation process required. Carbon from combusted artefacts must be incorporated into a solid metallic target from which a negative ion beam is produced and accelerated to MeV energies by an accelerator for subsequent analysis. This paper will describe a novel technique being developed by the National Ocean Sciences Accelerator Mass Spectrometry (NOSAMS) Laboratory at the Woods Hole Oceanographic Institution for the production of negative carbon ion beams directly from a continuously flowing sample gas stream, eliminating the requirement for a solid target. A key component of the new technique is a microwave-driven, gaseous-feed ion source originally developed at Chalk River Laboratories for the very different requirements of a high current proton linear accelerator. A version of this ion source is now being adapted to serve as an injector for a dedicated AMS accelerator facility at NOSAMS. The paper begins with a review of the fundamentals of radiocarbon dating. Experiments carried out at NOSAMS with a prototype of the microwave ion source are described, including measurements of sample utilization efficiency and sample 'memory' effect. A new version of the microwave ion source, optimized for AMS, is also described. The report concludes with some predictions of new research opportunities that will become accessible to the technique of continuous-flow AMS. (author)

  2. 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)

  3. Issues and opportunities in accelerator mass spectrometry for stable isotopes.

    Science.gov (United States)

    Matteson, Sam

    2008-01-01

    Accelerator mass spectrometry (AMS) has developed in the last 30 years many notable applications to the spectrometry of radioisotopes, particularly in radiocarbon dating. The instrumentation science of trace element AMS (TEAMS) that analyzes stable isotopes, also called Accelerator SIMS or MegaSIMS, while unique in many features, has also shared in many of these significant advances and has pushed TEAMS sensitivity to concentration levels surpassing many competing mass spectroscopic technologies. This review examines recent instrumentation developments, the capabilities of the new instrumentation and discernable trends for future development. Copyright 2008 Wiley Periodicals, Inc.

  4. State of dog's metabolism in the remote period after the oxide tritium influence

    International Nuclear Information System (INIS)

    Kalistratova, V.S.; Tishchenko, G.S.; Bortnik, L.A.; Nisimov, P.G.; Romanova, I.B.

    2000-01-01

    Influence of tritium oxide on the metabolism by some indices of lipid metabolism (common lipids, β-lipoproteins, cholesterin), protein metabolism (cholinesterase) and carbohydrate metabolism (blood sugar) was studied. It was established that the introduction into organism of tritium oxide in the quantities, which could form lethal and sublethal doses of internal radiation, provoked the main changes of values of mentioned indices of metabolism. The character of metabolism changes in the remote period allows to judge about the development of sclerosis processes which can be the result of radiation-stipulated acceleration of organism aging [ru

  5. 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)

  6. 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)

  7. Interface for the rapid analysis of liquid samples by accelerator mass spectrometry

    Science.gov (United States)

    Turteltaub, Kenneth; Ognibene, Ted; Thomas, Avi; Daley, Paul F; Salazar Quintero, Gary A; Bench, Graham

    2014-02-04

    An interface for the analysis of liquid sample having carbon content by an accelerator mass spectrometer including a wire, defects on the wire, a system for moving the wire, a droplet maker for producing droplets of the liquid sample and placing the droplets of the liquid sample on the wire in the defects, a system that converts the carbon content of the droplets of the liquid sample to carbon dioxide gas in a helium stream, and a gas-accepting ion source connected to the accelerator mass spectrometer that receives the carbon dioxide gas of the sample in a helium stream and introduces the carbon dioxide gas of the sample into the accelerator mass spectrometer.

  8. 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

  9. 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

  10. Acceleration of the GrIS mass loss as observed by GRACE

    DEFF Research Database (Denmark)

    Svendsen, Peter Limkilde; Andersen, Ole Baltazar; Nielsen, Allan Aasbjerg

    2012-01-01

    The mass loss of the Greenland Ice Sheet (GrIS) has previously been analysed in a variety of ways, including altimetry, gravimetry and mass budget calculations, establishing a continuing decrease in the ice mass, with a number of studies finding acceleration in the mass loss. Here, we examine...

  11. 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.

  12. 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

  13. 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

  14. Tritium in nuclear power plants

    International Nuclear Information System (INIS)

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

    1981-01-01

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

  15. 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)

  16. 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)

  17. 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

  18. Computer automation of an accelerator mass spectrometry system

    International Nuclear Information System (INIS)

    Gressett, J.D.; Maxson, D.L.; Matteson, S.; McDaniel, F.D.; Duggan, J.L.; Mackey, H.J.; North Texas State Univ., Denton, TX; Anthony, J.M.

    1989-01-01

    The determination of trace impurities in electronic materials using accelerator mass spectrometry (AMS) requires efficient automation of the beam transport and mass discrimination hardware. The ability to choose between a variety of charge states, isotopes and injected molecules is necessary to provide survey capabilities similar to that available on conventional mass spectrometers. This paper will discuss automation hardware and software for flexible, high-sensitivity trace analysis of electronic materials, e.g. Si, GaAs and HgCdTe. Details regarding settling times will be presented, along with proof-of-principle experimental data. Potential and present applications will also be discussed. (orig.)

  19. Neutrino masses twenty-five years later

    International Nuclear Information System (INIS)

    Valle, J.W.F.

    2003-01-01

    The discovery of neutrino mass marks a turning point in elementary particle physics, with important implications for nuclear and astroparticle physics. Here I give a brief update, where I summarize the current status of three-neutrino oscillation parameters from current solar, atmospheric, reactor and accelerator neutrino data, discuss the case for sterile neutrinos and LSND, and also the importance of tritium and double beta decay experiments probing the absolute scale of neutrino mass. In this opinionated look at the present of neutrino physics, I keep an eye in the future, and a perspective of the past, taking the opportunity to highlight Joe Schechter's pioneering contribution, which I have had the fortune to share, as his PhD student back in the early eighties

  20. Determination of "1"3"5Cs by accelerator mass spectrometry

    International Nuclear Information System (INIS)

    MacDonald, C.M.; Charles, C.R.J.; Zhao, X.-L.; Kieser, W.E.; Cornett, R.J.; Litherland, A.E.

    2015-01-01

    The ratio of anthropogenic "1"3"5Cs and "1"3"7Cs isotopes is characteristic of a uranium fission source. This research evaluates the technique of isotope dilution (yield tracing) for the purpose of quantifying "1"3"5Cs by accelerator mass spectrometry with on-line isobar separation. Interferences from Ba, Zn_2, and isotopes of equal mass to charge ratios were successfully suppressed. However, some sample crosstalk from source contamination remains. The transmission and di-fluoride ionization efficiencies of Cs isotopes were found to be 8 × 10"−"3 and 1.7 × 10"−"7 respectively. This quantification of "1"3"5Cs using yield tracing by accelerator mass spectrometry shows promise for future environmental sample analysis once the issues of sample crosstalk and low efficiency can be resolved.

  1. Tritium in the western Mediterranean Sea during 1981 Phycemed cruise

    Science.gov (United States)

    Andrie, Chantal; Merlivat, Liliane

    1988-02-01

    We report on simultaneous hydrological and tritium data taken in the western Mediterranean Sea during April 1981 and which implement our knowledge of the spatial and temporal variability of the convection process occurring in the Northern Basin (Gulf of Lion, Ligurian Sea). The renewal time of the deep waters in the Medoc area is calculated to be 11 ± 2 years using a box-model assymption. An important local phenomenon of "cascading" off the Ebro River near the Spanish coast is, noticeable by the use of tritium data. In the Sardinia Straits area tritium data indicate very active mixing between 100 and 500 m depth. The tritium subsurface maxima in Sardinia Straits suggests the influence of not only the Levantine Intermediate Water (LIW) but also an important shallower component. In waters deeper than 500m, an active mixing occurs between the deep water and the LIW via an intermediate water mass from the Tyrrhenian Sea by "salt-fingering". Assuming a two end-member mixing. We determine the deep tritium content in the Sardinia Channel to be 1.8 TU. For comparison, the deep tritium content of the Northern Basin is equal to 1.3 TU. Tritium data relative to the Alboran Sea show that a layer of high tritium content persists all along its path from Sardifia to Gibraltar on a density surface shallower than the intermediate water. The homogeneity of the deep tritium concentrations between 1200 m depth and the bottom corroborate the upward "pumping" and westward circulation of deep waters along the continental slope of the North African Shelf. From the data measured in the Sardinia Straits and in the Alboran Sea, and upper limit of the deep advection rate of the order of 0.5 cm s-1 is estimated.

  2. 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.)

  3. 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

  4. 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)

  5. 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

  6. Present and future prospects of accelerator mass spectrometry

    International Nuclear Information System (INIS)

    Kutschera, W.

    1987-04-01

    Accelerator Mass Spectrometry (AMS) has become a powerful technique for measuring extremely low abundances (10 -10 to 10 -15 relative to stable isotopes) of long-lived radioisotopes with half-lives in the range from 10 2 to 10 8 years. With a few exceptions, tandem accelerators turned out to be the most useful instruments for AMS measurements. Both natural (mostly cosmogenic) and man-made (anthropogenic) radioisotopes are studied with this technique. In some cases very low concentrations of stable isotope are also measured. Applications of AMS cover a large variety of fields including anthropology, archaeology, oceanography, hydrology, climatology, volcanology, minerals exploration, cosmochemistry, meteoritics, glaciology, sedimentary processes, geochronology, environmental physics, astrophysics, nuclear and particle physics. Present and future prospects of AMS are discussed as an interplay between the continuous development of new techniques and the investigation of problems in the above mentioned fields. Typical factors to be considered are energy range and type of accelerator, and the possibilities of dedicated versus partial use of new or existing accelerators

  7. Applications of accelerator mass spectrometry: advances and innovation

    International Nuclear Information System (INIS)

    Fifield, L.K.

    2004-01-01

    Emerging trends in the applications of accelerator mass spectrometry (AMS) are identified and illustrated with specific examples. Areas of application covered include rapid landscape evolution, calibration of the radiocarbon time scale, compound-specific radiocarbon studies, tracing of nuclear discharges, and searches for extraterrestrial isotopes

  8. Mass, charge, and energy separation by selective acceleration with a traveling potential hill

    Science.gov (United States)

    Tung, L. Schwager; Barr, W. L.; Lowder, R. S.; Post, R. F.

    1996-10-01

    A traveling electric potential hill has been used to generate an ion beam with an energy distribution that is mass dependent from a monoenergetic ion beam of mixed masses. This effect can be utilized as a novel method for mass separation applied to identification or enrichment of ions (e.g., of elements, isotopes, or molecules). This theory for mass-selective acceleration is presented here and is shown to be confirmed by experiment and by a time-dependent particle-in-cell computer simulation. Results show that monoenergetic ions with the particular mass of choice are accelerated by controlling the hill potential and the hill velocity. The hill velocity is typically 20%-30% faster than the ions to be accelerated. The ability of the hill to pickup a particular mass uses the fact that small kinetic energy differences in the lab frame appear much larger in the moving hill frame. Ions will gain energy from the approaching hill if their relative energy in the moving hill frame is less than the peak potential of the hill. The final energy of these accelerated ions can be several times the source energy, which facilitates energy filtering for mass purification or identification. If the hill potential is chosen to accelerate multiple masses, the heaviest mass will have the greatest final energy. Hence, choosing the appropriate hill potential and collector retarding voltage will isolate ions with the lightest, heaviest, or intermediate mass. In the experimental device, called a Solitron, purified 20Ne and 22Ne are extracted from a ribbon beam of neon that is originally composed of 20Ne:22Ne in the natural ratio of 91:9. The isotopic content of the processed beam is determined by measuring the energy distribution of the detected current. These results agree with the theory. In addition to mass selectivity, our theory can also be applied to the filtration of an ion beam according to charge state or energy. Because of this variety of properties, the Solitron is envisioned to

  9. 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

  10. Dose contribution from metabolized organically bound tritium after acute tritiated water intakes in humans

    International Nuclear Information System (INIS)

    Trivedi, A.; Galeriu, D.; Richardson, R.B.

    1997-01-01

    Urine samples from eight male radiation workers who had an unplanned acute tritiated water intake were measured for tritium-in-urine up to 300 d post-exposure. During the first month or so post-exposure, these individuals increased their fluid intakes to accelerate the turnover rate of tritium in the body for dose mitigation. Their daily fluid intakes reverted to normal levels in the latter period of the study. A non-linear regressional analysis of the tritium-in-urine data showed that the average biological half-life of tritium in body water, with standard deviation, was 63 ± 1.0 d (range, 5.0-8.1 d) and 8.4 ± 2.0 d (range, 6.2-12.8 d) during the respective periods of increased fluid intake and the later period of normal fluid intake. A longer term component of tritium excretion was also observed with average biological half-life of 74 ± 18 d (range, 58-104 d), indicating the incorporation of tritium, and its retention, in the organic fractions of the body. A mathematical model was developed and used to estimate the dose increase from the metabolized organically bound tritium on the basis of the kinetics of tritium-in-urine. The model accounts for a change in the rates of urinary excretion caused by variable fluid intakes. The average dose to the body, for the eight male workers, due to the metabolized organically bound tritium was estimated to be 6.2 ± 1.3% (range, 3.5% to 8.9%) of the committed effective dose due to tritium in the body water. This value for the dose increase from organically bound tritium is in the range of the current recommendations of the International Commission on Radiological Protection, i.e., organically bound tritium incorporated into the body contributes about 10% of the dose to the body water following tritiated water intakes. (author)

  11. Effect of excess ozone on UV-stimulated tritium oxidation

    International Nuclear Information System (INIS)

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

    1995-01-01

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

  12. 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

  13. 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

  14. Analysis of tritium behaviour and recovery from a water-cooled Pb17Li blanket

    International Nuclear Information System (INIS)

    Malara, C.; Casini, G.; Viola, A.

    1995-01-01

    The question of the tritium recovery in water-cooled Pb17Li blankets has been under investigation for several years at JRC Ispra. The method which has been more extensively analysed is that of slowly circulating the breeder out from the blanket units and of extracting the tritium from it outside the plasma vacuum vessel by helium gas purging or vacuum degassing in a suited process apparatus. A computerized model of the tritium behaviour in the blanket units and in the extraction system was developed. It includes four submodels: (1) tritium permeation process from the breeder to the cooling water as a function of the local operative conditions (tritium concentration in Pb17Li, breeder temperature and flow rate); (2) tritium mass balance in each breeding unit; (3) tritium desorption from the breeder material to the gas phase of the extraction system; (4) tritium extraction efficiency as a function of the design parameters of the recovery apparatus. In the present paper, on the basis of this model, a parametric study of the tritium permeation rate in the cooling water and of the tritium inventory in the blanket is carried out. Results are reported and discussed in terms of dimensionless groups which describe the relative effects of the overall resistance on tritium transfer to the cooling water (with and without permeation barriers), circulating Pb17Li flow rate and extraction efficiency of the tritium recovery unit. The parametric study is extended to the recovery unit in the case of tritium extraction by helium purge or vacuum degassing in a droplet spray unit. (orig.)

  15. The Tritium White Paper

    International Nuclear Information System (INIS)

    2009-01-01

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

  16. The nucleic acid metabolism in rat liver after single and long-term administration of tritium oxide

    International Nuclear Information System (INIS)

    Shorokhova, V.B.

    1984-01-01

    It was shown that after a single administration of tritiUm oxide in a dose of 22.2 MBq/g body mass the liver mass increased, the concentration of nucleic acids decreased and the biosynthesjs rate increased dUring a one-month observation. By the end of the observation period (the first year) the parameters under study were normalized. The long-term administration of tritium oxide in daily doses of 0.37, 0.925 and 1.85 MBq/g body mass caused changes in the nucleac acid metabolism which were less manifest (at early times), than in the case of a single injection. At the same time, the long-term administration of tritium oxide in the dose of 0.925 MBq/g caused a substantial disturbance of the nucleic acid metabolism at later times (after 2-9 months)

  17. 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

  18. 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.

  19. 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

  20. 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

  1. 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

  2. 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

  3. Scoping calculations for groundwater transport of tritium from the Gnome Site, New Mexico

    International Nuclear Information System (INIS)

    Pohlmann, K.; Andricevic, R.

    1994-08-01

    Analytic solutions are employed to investigate potential groundwater transport of tritium from a radioactive tracer site near the Project Gnome site in southeastern New Mexico. The tracer test was conducted in 1963 and introduced significant quantities of radionuclides to the transmissive and laterally continuous Culebra dolomite. Groundwater in the Culebra near Gnome travels toward a regional discharge point at the Pecos River, a distance of about 10 to 15 km, depending on flow path. Groundwater transport of radionuclides from the Gnome site is therefore of interest due to the proximity of the accessible environment and the 31-year time period during which migration is likely to have occurred. The analytical stochastic solutions used incorporate the heterogeneity observed in the Culebra by treating transmissivity as a spatially correlated random field. The results indicate that significant spreading of tritium will occur in the Culebra dolomite as a result of the combination of relatively high transmissivity, high spatial variability, and high spatial correlation of transmissivity. Longitudinal spreading may cause a very small fraction of tritium mass to arrive at the Pecos River within the 31 years since the tracer test. However, dilution and transverse dispersion will act to distribute this mass over a very large volume, thereby reducing groundwater concentrations. Despite the high degree of spreading, the calculations indicate that most of the tritium remains near the source. At present, the center of mass is estimated to have moved approximately 260 m downgradient of the test location and about 95 percent of the mass is estimated to have remained within about 1 km downgradient

  4. 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

  5. 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)

  6. Tritium in plants

    International Nuclear Information System (INIS)

    Vichot, L.; Losset, Y.

    2009-01-01

    The presence of tritium in the environment stems from its natural production by cosmic rays, from the fallout of the nuclear weapon tests between 1953 and 1964, and locally from nuclear industry activities. A part of the tritiated water contained in the foliage of plants is turned into organically bound tritium (OBT) by photosynthesis. The tritium of OBT, that is not exchangeable and then piles up in the plant, can be used as a marker of the past. It has been shown that the quantity of OBT contained in the age-rings of an oak that grew near the CEA center of Valduc was directly correlated with the tritium releases of the center. (A.C.)

  7. 36Chlorine accelerator mass spectrometry programme at BARC-TIFR pelletron accelerator. RSP-12

    International Nuclear Information System (INIS)

    Surendran, P.; Shrivastava, A.; Gupta, A.K.; Nair, J.P.; Yadav, M.L.; Gore, J.A.; Sparrow, H.; Bhagwat, P.V.; Kailas, S.; Kale, R.M.; Hemalatha, M.

    2007-01-01

    Accelerator mass spectrometry (AMS) is an ultra sensitive means of counting individual atoms having sufficiently long half life and available in small amount. The 14 UD Pelletron Accelerator is an ideal machine to carry out AMS studies with heavy isotopes like 36 Cl and 129 I. Cosmogenic radio isotope 36 Cl is widely being detected using AMS as it has got applications in ground water research, radioactive waste management, atmospheric 36 Cl transport mechanism studies of Arctic Alpine ice core etc. As a part of the ongoing AMS programme at 14UD Pelletron Accelerator Facility, Mumbai, a segmented gas detector developed for identification of 36 Cl was tested for performance. Recently a beam chopper required for this measurement has been developed. 36 Cl measurements carried out to detect and measure the ratio of 36 Cl to 35 Cl in an irradiated sample and dated sample are reported in this paper

  8. 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)

  9. A critical analysis of the impact assessment of environmental tritium

    International Nuclear Information System (INIS)

    Jain, Narendra; Bhatia, Arvind

    2013-01-01

    Tritium, a radionuclide of hydrogen has longer life and gets more rapidly dispersed, but before becoming globally distributed, it represents a significant radiobiological risk to the local population exposed. It is produced naturally in the upper atmosphere by the interaction of cosmic rays with nitrogen and hydrogen. The tritons in the upper atmosphere are oxidized to tritiated water (HTO) and mix with the hydrosphere generally through the movement of air masses and precipitation. Terrestrially, tritium may be formed by the action of lithium on neutrons. There is apprehension that the recent controversy concerning the health and environmental impact of tritium may end up as worldwide contaminants in the final analysis. From many varied reports from different laboratories, it appears that projected levels for fusion reactors may also produce deleterious and detectable effects. The degree of concern over tritium problem is evidenced by a rapid increase in publications on the health implications of environmental tritium. The present issues of controversy will be intensified as the fusion reactor technology approaches the door step of public and the possible health detriment from its radioactive emissions arouse concern. The current project has been planned keeping some such points in view. It reviews the work on the behavior of tritium in its various forms in the environment with an emphasis on the release from various sources, its world inventories at present level sand its transfer into the various compartments of ecosystems. Besides this, its metabolism in biosystem and the possible implications of low doses of tritium in present and future generations have also been discussed. (author)

  10. Tritium concentrations in tree ring cellulose

    International Nuclear Information System (INIS)

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

    1989-01-01

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

  11. 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%

  12. 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)

  13. Accelerator mass spectrometry of 41Ca with a positive-ion source and the UNILAC accelerator

    International Nuclear Information System (INIS)

    Steinhof, A.; Henning, W.; Mueller, M.; Roeckl, E.; Schuell, D.; Korschinek, G.; Nolte, E.; Paul, M.

    1987-06-01

    We have made first tests investigating the performance characteristics of the UNILAC accelerator system at GSI, in order to explore the sensitivity achievable in accelerator mass spectrometry (AMS) of 41 Ca with high-current positive-ion sources. Positively charged Ca 3+ ions of up to about 100 micro-amperes electrical current were injected from a penning-sputter source and, after further stripping to Ca 9+ , accelerated to 14.3 MeV/nucleon. The combination of velocity-focussing accelerator and magnetic ion-beam transport system completely eliminated background from the other calcium isotopes. Full-stripping and detection of 41 Ca 20+ ions with a magnetic spectrograph provides separation from isobaric 41 K and, at present, a level of sensitivity of 41 Ca/Ca ≅ 2x10 -15 . Future improvements and implications for dating of Pleistoscene samples will be discussed. (orig.)

  14. 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)

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

    International Nuclear Information System (INIS)

    Dautel, W.A.

    1996-01-01

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

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

    Energy Technology Data Exchange (ETDEWEB)

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

    2015-03-15

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

  17. Tritium accounting for PHWR plants

    International Nuclear Information System (INIS)

    Nair, P.S.; Duraisamy, S.

    2012-01-01

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

  18. Heavy-ion accelerator mass spectrometry with a 'small' accelerator

    International Nuclear Information System (INIS)

    Steier, P.; Golser, R.; Priller, A.; Vockenhuber, C.; Irlweck, K.; Kutschera, W.; Lichtenstein, V.

    2001-01-01

    Full text: VERA, the Vienna environmental research accelerator, is based on a 3-MV pelletron tandem accelerator and is designed to allow the transport of ions of all elements, from the lightest to the heaviest. The VERA heavy ion program tries to establish measurement methods which work for the long-lived radionuclides where suppression of isobars is not required. Among these are 129 I, 210 Pb, 236 U and all heavier ions where no stable isobars exist. To suppress neighboring masses, the resolution of VERA was increased, both by improving the ion optics of existing elements and by installing a new electrostatic separator after the analyzing magnet. Interfering ions which pass all beam filters are identified with a high-resolution time-of-flight system, using a 0.5 μg/cm 2 DLC (diamond-like carbon) foil in the start detector, which substantially reduces beam straggling. Compared to heavy ion AMS at large tandem accelerators (TV ≥ 8 MV) and for cases where stable isobar interference is absent, it is possible to offset the disadvantage of lower ion energy. Moreover, the more compact facilities like VERA achieve higher stability and reliability and provide advanced computer control. This promises even higher precision and sensitivity for a larger number of samples, which is a prerequisite for research on natural-occurring heavy radioisotopes at environmental levels. First results on the measurement of 210 Pb (half-life 22 a) and 236 U (23 Ma) encourages us to push towards even heavier radionuclides (e.g. 224 Pu, 81 Ma). (author)

  19. 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.)

  20. Tritium oxidation and exchange: preliminary studies

    International Nuclear Information System (INIS)

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

    1978-05-01

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

  1. TFTR tritium operations lessons learned

    International Nuclear Information System (INIS)

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

    1996-01-01

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

  2. Problems of anthropogenic tritium limitation

    Directory of Open Access Journals (Sweden)

    Kochetkov О.A.

    2013-12-01

    Full Text Available This article contains the current situation in respect to the environmental concentrations of anthropogenic and natural tritium. There are presented and analyzed domestic standards for НТО of all Radiation Safety Standards (NRB, as well as the regulations analyzed for tritium in drinking water taken in other countries today. This article deals with the experience of limitation of tritium and focuses on the main problem of rationing of tritium — rationing of organically bound tritium.

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

    Energy Technology Data Exchange (ETDEWEB)

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

    2009-07-01

    The presence of tritium in the environment stems from its natural production by cosmic rays, from the fallout of the nuclear weapon tests between 1953 and 1964, and locally from nuclear industry activities. A part of the tritiated water contained in the foliage of plants is turned into organically bound tritium (OBT) by photosynthesis. The tritium of OBT, that is not exchangeable and then piles up in the plant, can be used as a marker of the past. It has been shown that the quantity of OBT contained in the age-rings of an oak that grew near the CEA center of Valduc was directly correlated with the tritium releases of the center. (A.C.)

  4. Exploration for tritium-free water

    International Nuclear Information System (INIS)

    Hussain, S.D.

    1982-10-01

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

  5. Fluorine 18 in tritium generator ceramic materials

    International Nuclear Information System (INIS)

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

    1992-01-01

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

  6. Tritium in the aquatic environment

    International Nuclear Information System (INIS)

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

    1986-02-01

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

  7. 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

  8. Tritium protective clothing

    International Nuclear Information System (INIS)

    Fuller, T.P.; Easterly, C.E.

    1979-06-01

    Occupational exposures to radiation from tritium received at present nuclear facilities and potential exposures at future fusion reactor facilities demonstrate the need for improved protective clothing. Important areas relating to increased protection factors of tritium protective ventilation suits are discussed. These areas include permeation processes of tritium through materials, various tests of film permeability, selection and availability of suit materials, suit designs, and administrative procedures. The phenomenological nature of film permeability calls for more standardized and universal test methods, which would increase the amount of directly useful information on impermeable materials. Improvements in suit designs could be expedited and better communicated to the health physics community by centralizing devlopmental equipment, manpower, and expertise in the field of tritium protection to one or two authoritative institutions

  9. Tritium protective clothing

    Energy Technology Data Exchange (ETDEWEB)

    Fuller, T. P.; Easterly, C. E.

    1979-06-01

    Occupational exposures to radiation from tritium received at present nuclear facilities and potential exposures at future fusion reactor facilities demonstrate the need for improved protective clothing. Important areas relating to increased protection factors of tritium protective ventilation suits are discussed. These areas include permeation processes of tritium through materials, various tests of film permeability, selection and availability of suit materials, suit designs, and administrative procedures. The phenomenological nature of film permeability calls for more standardized and universal test methods, which would increase the amount of directly useful information on impermeable materials. Improvements in suit designs could be expedited and better communicated to the health physics community by centralizing devlopmental equipment, manpower, and expertise in the field of tritium protection to one or two authoritative institutions.

  10. Technology developments for improved tritium management

    International Nuclear Information System (INIS)

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

    1994-06-01

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

  11. Results of monitoring of tritium behaviour and its concentration in the objects of Chernobylsk NPP environment

    International Nuclear Information System (INIS)

    Badyaev, V.V.; Egorov, Yu.A.; Korobejnikov, V.L.; Krasnozhen, G.N.; Stegachev, G.F.; Tolstykh, V.D.

    1985-01-01

    Results of systematic observations on tritium behaviur at the Chernobyl NPP in the system ''source of formation-environment'' are presented. Investigations were conducted in a stepwise manner. Investigations of the first step were performed in order to make an experimental basis of the tritium dynamic model. Tritium activity is determined in all NPP technological subsystems, in cooling reservoir and in the atmosphere. The dynamic model of tritium accumulation at NPP with LWGR-reactor and its exchange with environment is developed and studied at the second step. The third step of investigations includes studies of tritium behaviour in complex experiments along with the behaviour of other radionuclides present in NPP releases and effluents incidentally state of environmental objects is recorded. It is shown that tritium specific activity in atmosphere does not exceed the background values. Tritium activity in leaves of trees is equal to (5-7)x10 -11 Ci/kg of mass

  12. Thought experiment with tritium

    International Nuclear Information System (INIS)

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

    1995-01-01

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

  13. 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.

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

    International Nuclear Information System (INIS)

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

    1995-01-01

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

  15. Tritium emissions from a detritiation facility

    International Nuclear Information System (INIS)

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

    2010-01-01

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

  16. Technologies using accelerator-driven targets under development at BNL

    International Nuclear Information System (INIS)

    Van Tuyle, G.J.

    1994-01-01

    Recent development work conducted at Brookhaven National Laboratory on technologies which use particle accelerator-driven targets is summarized. These efforts include development of the Spallation-Induced Lithium Conversion (SILC) Target for the Accelerator Production of Tritium (APT), the Accelerator-Driven Assembly for Plutonium Transformation (ADAPT) Target for the Accelerator-Based Conversion (ABC) of excess weapons plutonium. The PHOENIX Concept for the accelerator-driven transmutation of minor actinides and fission products from the waste stream of commercial nuclear power plants, and other potential applications

  17. The ITER tritium systems

    International Nuclear Information System (INIS)

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

    2007-01-01

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

  18. Purification of tritium-free water

    International Nuclear Information System (INIS)

    Hussain, S.D.

    1982-10-01

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

  19. Limits on the electron-antineutrino mass

    International Nuclear Information System (INIS)

    Wilkerson, J.F.

    1987-01-01

    New measurements near the endpoint of the tritium beta-decay spectrum are producing limits on the electron-antineutrino mass which are below the central mass value of 30 eV reported by ITEP. The factors that influence the neutrino mass sensitivity of tritium beta decay measurements will be discussed followed by a review of the current experimental results. 9 refs., 5 figs., 2 tabs

  20. Tritium trick

    Science.gov (United States)

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

    1971-01-01

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

  1. Tritium breeding in fusion reactors

    International Nuclear Information System (INIS)

    Abdou, M.A.

    1982-10-01

    Key technological problems that influence tritium breeding in fusion blankets are reviewed. The breeding potential of candidate materials is evaluated and compared to the tritium breeding requirements. The sensitivity of tritium breeding to design and nuclear data parameters is reviewed. A framework for an integrated approach to improve tritium breeding prediction is discussed with emphasis on nuclear data requirements

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

    Energy Technology Data Exchange (ETDEWEB)

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

    2016-11-01

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

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

    International Nuclear Information System (INIS)

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

    2010-01-01

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

  4. Tritium in metals

    International Nuclear Information System (INIS)

    Schober, T.

    1990-01-01

    In this Chapter a review is given of some of the important features of metal tritides as opposed to hydrides and deuterides. After an introduction to the topics of tritium and tritium in metals information will be presented on a variety of metal-tritium systems. Of main interest here are the differences from the classic hydrogen behavior; the so called isotope effect. A second important topic is that of aging effects produced by the accumulation of 3 He in the samples. (orig.)

  5. Subattomole sensitivity in biological accelerator mass spectrometry.

    Science.gov (United States)

    Salehpour, Mehran; Possnert, Göran; Bryhni, Helge

    2008-05-15

    The Uppsala University 5 MV Pelletron tandem accelerator has been used to study (14)C-labeled biological samples utilizing accelerator mass spectrometry (AMS) technology. We have adapted a sample preparation method for small biological samples down to a few tens of micrograms of carbon, involving among others, miniaturizing of the graphitization reactor. Standard AMS requires about 1 mg of carbon with a limit of quantitation of about 10 amol. Results are presented for a range of small sample sizes with concentrations down to below 1 pM of a pharmaceutical substance in human blood. It is shown that (14)C-labeled molecular markers can be routinely measured from the femtomole range down to a few hundred zeptomole (10 (-21) mol), without the use of any additional separation methods.

  6. Behaviour of tritium in the environment

    International Nuclear Information System (INIS)

    1979-01-01

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

  7. Overview of tritium fast-fission yields

    International Nuclear Information System (INIS)

    Tanner, J.E.

    1981-03-01

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

  8. Tritium in rad waste management

    International Nuclear Information System (INIS)

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

    1990-01-01

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

  9. 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)

  10. Tritium waste package

    Science.gov (United States)

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

    1995-01-01

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

  11. 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)

  12. 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)

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

    International Nuclear Information System (INIS)

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

    2001-01-01

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

  14. Distribution and behavior of tritium in the environment near its sources

    International Nuclear Information System (INIS)

    Fukui, Masami

    1994-01-01

    Of the long-lived radionuclides migrating globally through the environment, tritium was investigated because it is a latent source of detectable pollution in the Kyoto University Research Reactor Institute (KURRI). Moreover, mass transport in an in situ situation could be studied as well. Discharge rates of tritium from the operation of reactors and reprocessing plants throughout the world are given together with data on the background level of tritium in the environment and the resulting collective effective dose equivalent commitment. The behavior of tritium that has leaked from a heavy water facility in the Kyoto University Research Reactor (KURR) is dealt with by modeling its transport between air, water, and building materials. The spatial distributions of tritium in the air within the facilities of the KURR and KUCA (Kyoto University Critical Assembly), as measured by a convenient monitoring method that uses small water basins as passive samplers also are shown. Tritium discharged as liquid effluents in a reservoir for monitoring and in a retention pond at the KURRI site was monitored, and its behavior clarified by use of a box model and/or a classical dispersion equation. The purpose of this research is to keep radiation exposure to workers and the public as low as reasonably achievable, taking into account economic and social considerations (the ALARA concept). (author)

  15. 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)

  16. 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.

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

    International Nuclear Information System (INIS)

    Velarde, Marta; Perlado, Manuel

    2001-01-01

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

  18. Tritium loss in molten flibe systems

    Energy Technology Data Exchange (ETDEWEB)

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

    2000-04-01

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

  19. 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

  20. Tritium loss in molten flibe systems

    International Nuclear Information System (INIS)

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

    2000-01-01

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

  1. Use of tritium and sources

    International Nuclear Information System (INIS)

    Noguchi, Hiroshi

    1997-01-01

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

  2. 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

  3. Design and construction of thermal desorption measurement system for tritium contained materials

    International Nuclear Information System (INIS)

    Hara, M.; Hatano, Y.; Calderoni, P.; Shimada, M.

    2014-01-01

    The dual-mode thermal desorption analysis system was designed and built in Idaho National Laboratory (INL) to examine the evolution of the hydrogen isotope gas from materials. The system is equipped with a mass spectrometer for stable hydrogen isotopes and an ionization chamber for tritium components. The performance of the system built was tested with using tritium contained materials. The evolution of tritiated gas species from contaminated materials was measured successfully by using the system. (author)

  4. 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.

  5. Preparation of a tritium Q-value measurement in a double penning trap

    Energy Technology Data Exchange (ETDEWEB)

    Diehl, Christoph; Orth, Christoph; Blaum, Klaus [Max-Planck-Institut fuer Kernphysik, Heidelberg (Germany); Physikalisches Institut, Ruprecht-Karls-Universitaet, Heidelberg (Germany); Pinegar, David [Max-Planck-Institut fuer Kernphysik, Heidelberg (Germany); Van Dyck, Robert Jr. [Department of Physics, University of Washington, Seattle (United States)

    2009-07-01

    A precise determination of the Q-value of tritium ({sup 3}H) is of relevance for the determination of the electron anti-neutrino mass as aspired by the Karlsruhe Tritium Neutrino Experiment (KATRIN). In our double Penning trap mass spectrometer we aim to measure the mass ratio of {sup 3}H and its {beta}-decay product {sup 3}He to an accuracy of 10{sup -11}, which would determine the Q-value to an accuracy of 30 meV. The spectrometer we utilize is an enhanced version of the University of Washington Penning trap mass spectrometer (UW-PTMS) and was recently transfered from Seattle to Heidelberg, where it is set up at the moment as the MPIK/UW-PTMS. We present the necessary preparation work at the Max-Planck-Institut fuer Kernphysik. This includes major reconstructions of the building as well as studies and control of environmental parameters in the laboratory, like temperature and magnetic field.

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

    Energy Technology Data Exchange (ETDEWEB)

    Dautel, W.A.

    1996-10-01

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

  7. Overview of the tritium system of Ignitor

    International Nuclear Information System (INIS)

    Rizzello, C.; Tosti, S.

    2008-01-01

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

  8. Neutrino mass and mixing, and non-accelerator experiments

    International Nuclear Information System (INIS)

    Robertson, R.G.H.

    1992-01-01

    We review the current status of experimental knowledge about neutrinos derived from kinematic mass measurements, neutrino oscillation searches at reactors and accelerators, solar neutrinos, atmospheric neutrinos, and single and double beta decay. The solar neutrino results yield fairly strong and consistent indication that neutrino oscillations are occurring. Other evidence for new physics is less consistent and convincing

  9. Development and Verification of Tritium Analyses Code for a Very High Temperature Reactor

    International Nuclear Information System (INIS)

    Oh, Chang H.; Kim, Eung S.

    2009-01-01

    A tritium permeation analyses code (TPAC) has been developed by Idaho National Laboratory for the purpose of analyzing tritium distributions in the VHTR systems including integrated hydrogen production systems. A MATLAB SIMULINK software package was used for development of the code. The TPAC is based on the mass balance equations of tritium-containing species and a various form of hydrogen (i.e., HT, H2, HTO, HTSO4, and TI) coupled with a variety of tritium source, sink, and permeation models. In the TPAC, ternary fission and neutron reactions with 6Li, 7Li 10B, 3He were taken into considerations as tritium sources. Purification and leakage models were implemented as main tritium sinks. Permeation of HT and H2 through pipes, vessels, and heat exchangers were importantly considered as main tritium transport paths. In addition, electrolyzer and isotope exchange models were developed for analyzing hydrogen production systems including both high-temperature electrolysis and sulfur-iodine process. The TPAC has unlimited flexibility for the system configurations, and provides easy drag-and-drops for making models by adopting a graphical user interface. Verification of the code has been performed by comparisons with the analytical solutions and the experimental data based on the Peach Bottom reactor design. The preliminary results calculated with a former tritium analyses code, THYTAN which was developed in Japan and adopted by Japan Atomic Energy Agency were also compared with the TPAC solutions. This report contains descriptions of the basic tritium pathways, theory, simple user guide, verifications, sensitivity studies, sample cases, and code tutorials. Tritium behaviors in a very high temperature reactor/high temperature steam electrolysis system have been analyzed by the TPAC based on the reference indirect parallel configuration proposed by Oh et al. (2007). This analysis showed that only 0.4% of tritium released from the core is transferred to the product hydrogen

  10. Linear induction accelerator for heavy ions

    International Nuclear Information System (INIS)

    Keefe, D.

    1976-01-01

    There is considerable recent interest in the use of high energy heavy ions to irradiate deuterium-tritium pellets in a reactor vessel to constitute a power source at the level of 1 GW or more. Various accelerator configurations involving storage rings have been suggested. This paper discusses how the technology of linear induction accelerators - well known to be matched to high current and short pulse length - may offer significant advantages for this application. (author)

  11. Oxidation of tritium by hopcalite bed

    Energy Technology Data Exchange (ETDEWEB)

    Nishikawa, Masabumi; Shinnai, Kohsuke; Matsunaga, Sohichi; Kinoshita, Yoshihiko

    1984-08-01

    Oxidation by the catalyst bed with a metal oxide and subsequent adsorption to the porous dehydrative reagents is supposed to be effective process for scavenging tritium from an inert atmosphere. Use of spongy copper oxide or wires of copper oxide is not recommended to use as the metal oxide catalyst from the view point of mass transfer because of sintering and of limited effective surface area. Use of hopcalites and copper oxide-kieselguhr are examined in this study and it is concluded that hopcalites are more suitable as the metal oxide catalyst because they not only remain the oxidation power on hydrogen isotopes even at an ambient temperature, but also show a negligible drop in oxidation performances with repeated regeneration. The effective temperature is about 400/sup 0/C for hopcalites and 300-600/sup 0/C for copper oxide-kieselguhr to use as the oxidation bed of tritium.

  12. Oxidation of tritium by hopcalite bed

    International Nuclear Information System (INIS)

    Nishikawa, Masabumi; Shinnai, Kohsuke; Matsunaga, Sohichi; Kinoshita, Yoshihiko

    1984-01-01

    Oxidation by the catalyst bed with a metal oxide and subsequent adsorption to the porous dehydrative reagents is supposed to be effective process for scavenging tritium from an inert atmosphere. Use of spongy copper oxide or wires of copper oxide is not recommended to use as the metal oxide catalyst from the view point of mass transfer because of sintering and of limited effective surface area. Use of hopcalites and copper oxide-kieselguhr are examined in this study and it is concluded that hopcalites are more suitable as the metal oxide catalyst because they not only remain the oxidation power on hydrogen isotopes even at an ambient temperature, but also show a negligible drop in oxidation performances with repeated regeneration. The effective temperature is about 400 0 C for hopcalites and 300--600 0 C for copper oxide-kieselguhr to use as the oxidation bed of tritium. (author)

  13. Tritium breeding blanket

    International Nuclear Information System (INIS)

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

    1991-01-01

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

  14. Acceleration Signal Characteristics for Intuitional Mass Analysis of Metallic Loose Parts

    International Nuclear Information System (INIS)

    Lee, Kwang-Hyun; Jung, Chang-Gyu

    2016-01-01

    Nuclear power plants (NPPs) have operated LPMS (Loose Parts Monitoring System) for early detection of the possible presence of metallic parts in the reactor coolant system (RCS); however, analysis of the metallic impact wave characteristics in the LPMS is an important issue because information, such as the mass of the metallic part and the impact location, is not provided. Most studies have concentrated on fieldwork using the frequency characteristics for the analysis of the metallic part mass. Thus, the field engineers cannot analyze signals without special software and access to the system. This paper is intended to introduce a process of intuitional mass analysis using the attenuation rate of the acceleration signal and the intervals between peak signals. Most studies related to mass analysis of a metallic part impact signal in LPMS have used the frequency spectrum. This paper presents a method of using the acceleration signal characteristics for intuitional mass analysis of loose metallic parts. With the method proposed in this paper, because the mass of a metallic part can be understood intuitionally without any special analysis program, intuitional analysis used in parallel with frequency spectrum analysis will be in effect

  15. Acceleration Signal Characteristics for Intuitional Mass Analysis of Metallic Loose Parts

    Energy Technology Data Exchange (ETDEWEB)

    Lee, Kwang-Hyun; Jung, Chang-Gyu [KHNP CRI, Daejeon (Korea, Republic of)

    2016-10-15

    Nuclear power plants (NPPs) have operated LPMS (Loose Parts Monitoring System) for early detection of the possible presence of metallic parts in the reactor coolant system (RCS); however, analysis of the metallic impact wave characteristics in the LPMS is an important issue because information, such as the mass of the metallic part and the impact location, is not provided. Most studies have concentrated on fieldwork using the frequency characteristics for the analysis of the metallic part mass. Thus, the field engineers cannot analyze signals without special software and access to the system. This paper is intended to introduce a process of intuitional mass analysis using the attenuation rate of the acceleration signal and the intervals between peak signals. Most studies related to mass analysis of a metallic part impact signal in LPMS have used the frequency spectrum. This paper presents a method of using the acceleration signal characteristics for intuitional mass analysis of loose metallic parts. With the method proposed in this paper, because the mass of a metallic part can be understood intuitionally without any special analysis program, intuitional analysis used in parallel with frequency spectrum analysis will be in effect.

  16. Results of observations of the tritium concentration in water fractions in the disposition regions of tritium laboratories

    International Nuclear Information System (INIS)

    Koval, G.N.; Kuzmina, A.I.; Kolomiets, N.F.; Svarichevskaya, E.V.; Rogosin, V.N.; Svyatun, O.V.

    1995-01-01

    In this paper results of the long term of control of tritium concentration in the water fractions in the region close to the tritium laboratories of INR NAS of Ukraine are presented. The regular observations for the tritium concentration in the water fractions (thawed water of the snow cover, birch juice and sewer water) in the influence region of tritium laboratories shows small amount of tritium concentration in all kinds of investigated water fractions in comparison with the tritium concentration in the reper points. The proper connection of the levels of tritium concentration of the water samples with the quantity of the technology production is observed. In common, the tritium pollution on the territory of INR shows the tendency for a considerable decrease of the environmental pollution levels from year to year. It can be explained by the perfection of the production technology of tritium structures and targets as well as the rising of the qualification of the personnel. 3 refs., 4 figs

  17. Tritium in the environment. Knowledge synthesis

    International Nuclear Information System (INIS)

    2009-01-01

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

  18. 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

  19. Tritium containment of controlled thermonuclear fusion reactor

    International Nuclear Information System (INIS)

    Tanaka, Yoshihisa; Tsukumo, Kiyohiko; Suzuki, Tatsushi

    1979-01-01

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

  20. Tritium problems in fusion reactor systems

    International Nuclear Information System (INIS)

    Hickman, R.G.

    1975-01-01

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

  1. Tritium transport and control in the FED

    International Nuclear Information System (INIS)

    Rogers, M.L.

    1981-01-01

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

  2. Present and future prospects of accelerator mass spectrometry

    Energy Technology Data Exchange (ETDEWEB)

    Kutschera, W

    1988-05-20

    Accelerator mass spectrometry (AMS) has become a powerful technique for measuring extremely low abundances (10/sup -10/ to 10/sup -15/ relative to stable isotopes) of long-lived radioisotopes with half-lives in the range from 10/sup 2/ to 10/sup 8/ years. With a few exceptions, tandem accelerators turned out to be the most useful instruments for AMS measurements. Both natural (mostly cosmogenic) and manmade (anthropogenic) radioisotopes are studied with this technique. In some cases very low concentrations of stable isotopes are also measured. Applications of AMS cover a large variety of fields including anthropology, archaeology, oceanography, hydrology, climatology, volcanology, mineral exploration, cosmochemistry, meteoritics, glaciology, sedimentary processes, geochronology, environmental physics, astrophysics, nuclear and particle physics. Present and future prospects of AMS will be discussed as an interplay between the continuous development of new techniques and the investigation of problems in the above mentioned field. Depending on the specific problem to be investigated, different aspects of an AMS system are of importance. Typical factors to be considered are energy range and type of accelerator, and the possibilities of dedicated versus partial use of new or existing accelerators.

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

    International Nuclear Information System (INIS)

    Gilligan, J.G.; Evans, K.

    1983-01-01

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

  4. The origin of mass and experiments on high-energy particle accelerators

    International Nuclear Information System (INIS)

    Ioffe, B.L.

    2006-01-01

    The visible world is one consisting of nucleons and electrons. The mass of nucleon arises from chiral symmetry breaking in quantum chromodynamics, so high energy accelerator experiments cannot give a clue to the nature of mass of matter in the visible world. The origin of the mass of the matter will be clarified when the mechanism of chiral symmetry breaking in quantum chromodynamics is established [ru

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

    International Nuclear Information System (INIS)

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

    1991-01-01

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

  6. Tritium accountancy in fusion systems

    Energy Technology Data Exchange (ETDEWEB)

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

    2015-03-15

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

  7. 14C Accelerator mass spectrometry in Brazil

    International Nuclear Information System (INIS)

    Macario, K.D.; Gomes, P.R.S.; Anjos, Roberto M.; Linares, R.; Queiroz, E.A.; Oliveira, F.M.; Cardozo, L.; Carvalho, C.R.A.

    2011-01-01

    Radiocarbon Accelerator Mass Spectrometry is an ultra-sensitive technique that enables the direct measurement of carbon isotopes in samples as small as a few milligrams. The possibility of dating or tracing rare or even compound specific carbon samples has application in many fields of science such as Archaeology, Geosciences and Biomedicine. Several kinds of material such as wood, charcoal, carbonate and bone can be chemically treated and converted to graphite to be measured in the accelerator system. The Physics Institute of Universidade Federal Fluminense (UFF), in Brazil will soon be able to perform the complete 14 C-AMS measurement of samples. At the Nuclear Chronology Laboratory (LACRON) samples are prepared and converted to carbon dioxide. A stainless steel vacuum system was constructed for carbon dioxide purification and graphitization is performed in sealed tubes in a muffle oven. Graphite samples will be analyzed in a 250 kV Single Stage Accelerator produced by National Electrostatic Corporation which will be installed in the beginning of 2012. With the sample preparation laboratory at LACRON and the SSAMS system, the Physics Institute of UFF will be the first 14 C-AMS facility in Latin America. (author)

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

    International Nuclear Information System (INIS)

    Diabate, S.; Strack, S.

    1990-12-01

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

  9. New method for laser driven ion acceleration with isolated, mass-limited targets

    International Nuclear Information System (INIS)

    Paasch-Colberg, T.; Sokollik, T.; Gorling, K.; Eichmann, U.; Steinke, S.; Schnuerer, M.; Nickles, P.V.; Andreev, A.; Sandner, W.

    2011-01-01

    A new technique to investigate laser driven ion acceleration with fully isolated, mass-limited glass spheres with a diameter down to 8μm is presented. A Paul trap was used to prepare a levitating glass sphere for the interaction with a laser pulse of relativistic intensity. Narrow-bandwidth energy spectra of protons and oxygen ions have been observed and were attributed to specific acceleration field dynamics in case of the spherical target geometry. A general limiting mechanism has been found that explains the experimentally observed ion energies for the mass-limited target.

  10. A prototype wearable tritium monitor

    International Nuclear Information System (INIS)

    Surette, R. A.; Dubeau, J.

    2008-01-01

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

  11. Tritium pellet injection sequences for TFTR

    International Nuclear Information System (INIS)

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

    1983-01-01

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

  12. Radionuclide Basics: Tritium

    Science.gov (United States)

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

  13. The effect of helium generation and irradiation temperature on tritium release from neutron irradiated beryllium

    International Nuclear Information System (INIS)

    Kupriyanov, I.B.; Gorokhov, V.A.; Vlasov, V.V.; Kovalev, A.M.; Chakin, V.P.

    2004-01-01

    The effect of neutron irradiation condition on tritium release from beryllium is described in this paper. Beryllium samples were irradiated in the SM reactor with neutron fluence (E > 0.1 MeV) of (0.37-2.0) x 10 22 cm -2 at 70-100degC and 650-700degC. Mass-spectrometer technique was used in out of tritium release experiments during stepped-temperature anneal within a temperature range from 250 to 1300degC. The total amount of helium accumulated in irradiated beryllium samples varied from 521 appm to 3061 appm. The first signs of tritium release were detected at temperature of 406-553degC. It was shown that irradiation temperature and helium generation level significantly affect the tritium release. A fraction of 44 - 74 % of tritium content in samples irradiated at low temperature (70 - 100degC) is release from beryllium at an annealing temperature below 800degC, whereas for samples after high temperature irradiation (650 - 700 degC) tritium release did not exceed 14 %. Majority of tritium (∼68%) is released within a temperature range from 800 to 920 degC. The increase of helium generation from 521 appm to 3061 appm results in lowering the temperature of maximal tritium release rate and the upper temperature of tritium release from beryllium by 100-130degC and 200-240degC, correspondingly. On the basis of data obtained, the diffusion coefficients of tritium in beryllium were calculated. (author)

  14. Characteristics of an electron-beam rocket pellet accelerator

    International Nuclear Information System (INIS)

    Tsai, C.C.; Foster, C.A.; Schechter, D.E.

    1989-01-01

    An electron-beam rocket pellet accelerator has been designed, built, assembled, and tested as a proof-of-principle (POP) apparatus. The main goal of accelerators based on this concept is to use intense electron-beam heating and ablation of a hydrogen propellant stick to accelerate deuterium and/or tritium pellets to ultrahigh speeds (10 to 20 km/s) for plasma fueling of next-generation fusion devices such as the International Thermonuclear Engineering Reactor (ITER). The POP apparatus is described and initial results of pellet acceleration experiments are presented. Conceptual ultrahigh-speed pellet accelerators are discussed. 14 refs., 8 figs

  15. Advancement in tritium transport simulations for solid breeding blanket system

    Energy Technology Data Exchange (ETDEWEB)

    Ying, Alice, E-mail: ying@fusion.ucla.edu [Mechanical and Aerospace Engineering Department, UCLA, Los Angeles, CA 90095 (United States); Zhang, Hongjie [Mechanical and Aerospace Engineering Department, UCLA, Los Angeles, CA 90095 (United States); Merrill, Brad J. [Idaho National Laboratory, Idaho Falls, ID 83415 (United States); Ahn, Mu-Young [National Fusion Research Institute, Daejeon (Korea, Republic of)

    2016-11-01

    In this paper, advancement on tritium transport simulations was demonstrated for a solid breeder blanket HCCR TBS, where multi-physics and detailed engineering descriptions are considered using a commercial simulation code. The physics involved includes compressible purge gas fluid flow, heat transfer, chemical reaction, isotope swamping effect, and tritium isotopes mass transport. The strategy adopted here is to develop numerical procedures and techniques that allow critical details of material, geometric and operational heterogeneity in a most complete engineering description of the TBS being incorporated into the simulation. Our application focuses on the transient assessment in view of ITER being pulsed operations. An immediate advantage is a more realistic predictive and design analysis tool accounting pulsed operations induced temperature variations which impact helium purge gas flow as well as Q{sub 2} composition concentration time and space evolutions in the breeding regions. This affords a more accurate prediction of tritium permeation into the He coolant by accounting correct temperature and partial pressure effects and realistic diffusion paths. The analysis also shows that by introducing by-pass line to accommodate ITER pulsed operations in the TES loop allows tritium extraction design being more cost effective.

  16. Accelerator mass spectrometry - From DNA to astrophysics

    International Nuclear Information System (INIS)

    Kutschera, W.

    2013-01-01

    A brief review of accelerator mass spectrometry (AMS) is presented. The present work touches on a few technical aspects and recent developments of AMS, and describes two specific applications of AMS, the dating of human DNA with the 14 C bomb peak and the search for superheavy elements in nature. Since two extended general reviews on technical developments in AMS [1] and applications of AMS [2] will appear in 2013, frequent reference to these reviews is made. (authors)

  17. Injection system of the minicyclotron accelerator mass spectrometer

    International Nuclear Information System (INIS)

    Liu Yonghao; Li Deming; Chen Maobai; Lu Xiangshun

    1999-01-01

    The existing injection system of the SMCAMS (super-sensitive mini-cyclotron accelerator mass spectrometer) is described together with the discussion of its disadvantages exposed after having been operating for five years, which provides a basis for consideration of improvements to the injection system. An optimized injection system with an analytical magnet added prior to the minicyclotron has been proposed and calculated

  18. 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.

  19. 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.)

  20. Tritium migration in nuclear desalination plants

    International Nuclear Information System (INIS)

    Muralev, E.D.

    2003-01-01

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

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

    International Nuclear Information System (INIS)

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

    2007-01-01

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

  2. 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)

  3. Tritium sorption by cement and subsequent release

    International Nuclear Information System (INIS)

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

    1994-01-01

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

  4. 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

  5. A proposed model for the transfer of environmental tritium to man and tritium metabolism in model animals

    International Nuclear Information System (INIS)

    Saito, Masahiro; Ishida, M.R.

    1987-01-01

    To evaluate the accumulated dose in human bodies due to the environmental tritium, it is of required to establish an adequate model for the tritium transfer from the environment to man and to obtain enough information on the metabolic behaviour of tritium in animal bodies using model animal system. In this report, first we describe about a proposed model for the transfer of environmental tritium to man and secondly mention briefly about the recent works on the tritium metabolism in newborn animals which have been treated as a model system of tritium intake through food chain. (author)

  6. Contribution to the tritium continental effect

    International Nuclear Information System (INIS)

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

    1987-01-01

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

  7. Age-dependent dose coefficients for tritium in Asian populations

    Energy Technology Data Exchange (ETDEWEB)

    Trivedi, A

    1999-10-01

    The International Commission on Radiological Protection (ICRP) Publications 56 (1989) and 67 (1993) have prescribed the biokinetic models and age-dependent dose coefficients for tritiated water and organically bound tritium. The dose coefficients are computed from values selected to specify the anatomical, morphological and physiological characteristics of a three-month-old, one-year-old, five-year-old, 10-year-old, 15-year-old and adult (Reference Man) Caucasian living in North America and Western Europe. However, values for Reference Man and other age groups are not directly applicable to Asians, because of differences in race, custom, dietary habits and climatic conditions. An Asian Man model, including five age groups, has been proposed by Tanaka and Kawamura (1996, 1998) for use in internal dosimetry. The basic concept of the ICRP Reference Man and the system describing body composition in ICRP Publication 23 (1975) were used. Reference values for Asians were given for the body weight and height, the mass of soft tissue, the mass of body water and the daily fluid balance, and are used to compute the dose coefficients for tritium. The age-dependent dose coefficients for Asians for tritiated water intakes are smaller by 20 to 30% of the currently prescribed values (Trivedi, 1998). The reduction in the dose coefficient values is caused by the increased daily fluid balance among Asians. The dose coefficient for tritiated water is 1.4 x 10{sup -11} Sv Bq{sup -1} for Asian Man compared to 2.0 x 10{sup -11} Sv Bq{sup -1} for Reference Man. The dose coefficients for organically bound tritium are only marginally different from those of the ICRP values. The dose coefficient for organically bound tritium for Asian Man is 4.0 x 10{sup -11} Sv Bq{sup -11} compared to 4.6 x 10{sup -11} Sv Bq{sup -1} for Reference Man. (author)

  8. Age-dependent dose coefficients for tritium in Asian populations

    International Nuclear Information System (INIS)

    Trivedi, A.

    1999-10-01

    The International Commission on Radiological Protection (ICRP) Publications 56 (1989) and 67 (1993) have prescribed the biokinetic models and age-dependent dose coefficients for tritiated water and organically bound tritium. The dose coefficients are computed from values selected to specify the anatomical, morphological and physiological characteristics of a three-month-old, one-year-old, five-year-old, 10-year-old, 15-year-old and adult (Reference Man) Caucasian living in North America and Western Europe. However, values for Reference Man and other age groups are not directly applicable to Asians, because of differences in race, custom, dietary habits and climatic conditions. An Asian Man model, including five age groups, has been proposed by Tanaka and Kawamura (1996, 1998) for use in internal dosimetry. The basic concept of the ICRP Reference Man and the system describing body composition in ICRP Publication 23 (1975) were used. Reference values for Asians were given for the body weight and height, the mass of soft tissue, the mass of body water and the daily fluid balance, and are used to compute the dose coefficients for tritium. The age-dependent dose coefficients for Asians for tritiated water intakes are smaller by 20 to 30% of the currently prescribed values (Trivedi, 1998). The reduction in the dose coefficient values is caused by the increased daily fluid balance among Asians. The dose coefficient for tritiated water is 1.4 x 10 -11 Sv Bq -1 for Asian Man compared to 2.0 x 10 -11 Sv Bq -1 for Reference Man. The dose coefficients for organically bound tritium are only marginally different from those of the ICRP values. The dose coefficient for organically bound tritium for Asian Man is 4.0 x 10 -11 Sv Bq -11 compared to 4.6 x 10 -11 Sv Bq -1 for Reference Man. (author)

  9. Tritium transport analysis for CFETR WCSB blanket

    Energy Technology Data Exchange (ETDEWEB)

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

    2017-01-15

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

  10. Tritium permeation and recovery

    International Nuclear Information System (INIS)

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

    1987-01-01

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

  11. The LLNL portable tritium processing system

    International Nuclear Information System (INIS)

    Anon.

    1995-01-01

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

  12. Estimation of Biological Effects of Tritium.

    Science.gov (United States)

    Umata, Toshiyuki

    2017-01-01

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

  13. Accelerator mass spectrometry for radiocarbon dating

    International Nuclear Information System (INIS)

    Bronk, C.R.

    1987-01-01

    Accelerator mass spectrometry (AMS) has been used routinely for radiocarbon measurements for several years. This thesis describes theoretical work to understand the reasons for low accuracy and range and offers practical solutions. The production and transport of the ions used in the measurements are found to be the most crucial stages in the process. The theories behind ion production by sputtering are discussed and applied to the specific case of carbon sputtered by caesium. Experimental evidence is also examined in relation to the theories. The phenomena of space charge and lens aberrations are discussed along with the interaction between ion beams and gas molecules in the vacuum. Computer programs for calculating phase space transformations are then described; these are designed to help investigations of the effects of space charge and aberrations on AMS measurements. Calculations using these programs are discussed in relation both to measured ion beam profiles in phase space and to the current dependent transmission of ions through the Oxford radiocarbon accelerator. Improvements have been made to this accelerator and these are discussed in the context of the calculations. C - ions are produced directly from carbon dioxide at the Middleton High Intensity Sputter Source. Experiments to evaluate the performance of such a source are described and detailed design criteria established. An ion source designed and built specifically for radiocarbon measurements using carbon dioxide is described. Experiments to evaluate its performance and investigate the underlying physical processes are discussed. (author)

  14. Importance of the virtual mass force in accelerating steam/water mixtures

    International Nuclear Information System (INIS)

    Khalil, Y.F.; Kazimi, M.S.

    1987-01-01

    Virtual mass force is one of the forces that must be considered against accelerating a dispersed fluid flowing in the bulk of a continuous fluid. This force depends on the geometry of the interface and the flow pattern of the two fluids. For dilute two-phase flow mixtures where the bubbles are singly dispersed, the value of the virtual mass force coefficient is dependent on the geometry of the bubble. However, for high void fraction cases, such as depressurization initiated by a pipe break in light water reactors, more intense interaction is expected between the two phase and, therefore, the value of the virtual mass force must be well defined. The effects of implementing the virtual mass force term in the momentum equations of a two-fluid model may be significant for improving the stability of the solution of the conservation equations, the accuracy of the numerical results, and the computation time. In the current work, a new stability criterion is derived after implementing Hancox's model for the virtual mass force in the momentum equations of the six-equation two-phase flow model of TERMIT. A one-dimensional blow-down in a horizontal pipe is considered to investigate the importance of incorporating the virtual mass force in accelerating mixtures flows

  15. Contribution to the tritium continental effect

    International Nuclear Information System (INIS)

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

    1987-01-01

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

  16. 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.)

  17. APT accelerator technology

    International Nuclear Information System (INIS)

    Schneider, J. David

    1996-01-01

    The proposed accelerator production of tritium (APT) project requires an accelerator that provides a cw proton beam of 100 m A at 1300 MeV. Since the majority of the technical risk of a high-current cw (continuous-wave, 100% DF) accelerator resides in the low-energy section, Los Alamos is building a 20 MeV duplicate of the accelerator front end to confirm design codes, beam performance, and demonstrate operational reliability. We report on design details of this low-energy demonstration accelerator (LEDA) and discuss the integrated design of the full accelerator for the APT plant. LEDA's proton injector is under test and has produced more than 130 mA at 75 keV. Fabrication is proceeding on a 6.7- MeV, 8-meter-long RFQ, and detailed design is underway on coupled-cavity drift-tube linac (CCDTL) structures. In addition, detailed design and technology experiments are underway on medium-beta superconducting cavities to assess the feasibility of replacing the conventional (room-temperature copper) high-energy linac with a linac made of niobium superconducting RF cavities. (author)

  18. Metabolism distribution and transfer of tritium in pregnant mice after exposure to tritium water

    International Nuclear Information System (INIS)

    Lu Huimin; Zhou Xiangyan; Li Li; Zhang Zhixing

    1993-01-01

    Tritium water with three kind of different dose was singly injected intraperitoneally to pregnant mice in various time. The tritium concentration in the tissues from mother mice were measured on the 3.5 days after mother mice parturition. Dose rates in baby mice were estimated, as well as the transfer coefficient of tritium from mother mice to baby mice was calculated based on the tritium concentrations. The results of the experiment showed that tritium was almost uniformly distributed among the tissues after exposure to tritiated water at three experimental groups. However, it was found that relative concentrations of tritium in the baby mice tissues were consistently higher than that in mother mice tissues for three experimental groups. The relative concentration of tritium in the tissues was not affected by the different dose but developing on the exposure time. The results of radiation dose rates from baby mice estimation at the end of exposure showed that the higher radiation dose rates was found in the mice exposed to tritiated water during 7.5 days. The transfer coefficient of tritium from mother mice into baby mice was almost no different among the three radiation dose groups. The highest transfer coefficient was observed in mother mice exposed to tritiated baby mice was almost no different among the three radiation dose groups. The highest coefficient was observed in mother mice exposed to tritiated water during 16.5 days, however it was not found that transfer coefficient were higher in the mother mice exposed to tritiated water during 11.5 days than that of 7.5 days

  19. Reactor prospects of muon-catalyzed fusion of deuterium and tritium concentrated in transition metals

    International Nuclear Information System (INIS)

    Stacey, W.M. Jr.

    1989-01-01

    It is conjectured that the number of fusion events catalyzed by a single muon is orders of magnitude greater for deuterium and tritium concentrated in a transition metal than in gaseous form and that the recent observation of 2.5-MeV neutrons from a D 2 O electrolytic cell with palladium and titanium cathodes can thereby be interpreted in terms of cosmic muon-catalyzed deuterium-deuterium fusion. This suggests a new fusion reactor reactor consisting of deuterium and tritium concentrated in transition metal fuel elements in a fusion core that surrounds an accelerator-produced muon source. The feasibility of net energy production in such a reactor is established in terms of requirements on the number of fusion events catalyzed per muon. The technological implications for a power reactor based on this concept are examined. The potential of such a concept as a neutron source for materials testing and tritium and plutonium production is briefly discussed

  20. 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.)

  1. Optimization of mass-production conditions for tritium breeder pebbles based on slurry droplet wetting method

    Energy Technology Data Exchange (ETDEWEB)

    Park, Yi-Hyun, E-mail: yhpark@nfri.re.kr [National Fusion Research Institute, Daejeon (Korea, Republic of); Min, Kyung-Mi; Ahn, Mu-Young; Cho, Seungyon; Lee, Young-Min [National Fusion Research Institute, Daejeon (Korea, Republic of); Park, Sang-Jin; Danish, Rehan; Lim, Chul-Hwan; Jo, Yong-Dae [IVT Co., Ltd., Daegu (Korea, Republic of)

    2016-11-01

    Highlights: • An automatic dispensing system was developed to improve uniformity and production rate of breeder pebbles. • The production rate of this system for Li{sub 2}TiO{sub 3} pebble was estimated at 50 kg/year. • The optimization of dispensing and sintering conditions for the mass-production of Li{sub 2}TiO{sub 3} pebble was conducted. • Integrity of Li{sub 2}TiO{sub 3} pebble was able to be ensured during mass-production process, especially during batch process. - Abstract: Lithium metatitanate (Li{sub 2}TiO{sub 3}) is being considered as tritium breeding material for solid-type breeding blanket, which are used in pebble-bed form. The total amount of Li{sub 2}TiO{sub 3} pebbles in Helium Cooled Ceramic Reflector (HCCR) Test Blanket Module (TBM) is approximately 80 kg. Furthermore, DEMO reactor requires a great deal of breeder pebbles. Therefore, the development of mass-production system for breeder pebbles is necessary. The slurry droplet wetting method was adopted in the mass-production process for Li{sub 2}TiO{sub 3} pebbles, which had been developed in Korea. In this method, an automatic slurry dispensing system is one of the key apparatuses because the uniformity of pebbles and production rate are able to be improved. The system was successfully manufactured, which was consisted of a dispensing unit for instillation of Li{sub 2}TiO{sub 3} slurry, a glycerin bath for hardening of droplets, and an automatic maintaining unit for constant distance between syringe needle and glycerin surface. The production rate of this system for Li{sub 2}TiO{sub 3} pebble was estimated at 50 kg/year. In this study, it was investigated that the effect of dispensing and sintering conditions on the mass-production of Li{sub 2}TiO{sub 3} pebbles.

  2. Measuring test mass acceleration noise in space-based gravitational wave astronomy

    Science.gov (United States)

    Congedo, Giuseppe

    2015-03-01

    The basic constituent of interferometric gravitational wave detectors—the test-mass-to-test-mass interferometric link—behaves as a differential dynamometer measuring effective differential forces, comprising an integrated measure of gravity curvature, inertial effects, as well as nongravitational spurious forces. This last contribution is going to be characterized by the LISA Pathfinder mission, a technology precursor of future space-borne detectors like eLISA. Changing the perspective from displacement to acceleration can benefit the data analysis of LISA Pathfinder and future detectors. The response in differential acceleration to gravitational waves is derived for a space-based detector's interferometric link. The acceleration formalism can also be integrated into time delay interferometry by building up the unequal-arm Michelson differential acceleration combination. The differential acceleration is nominally insensitive to the system's free evolution dominating the slow displacement dynamics of low-frequency detectors. Working with acceleration also provides an effective way to subtract measured signals acting as systematics, including the actuation forces. Because of the strong similarity with the equations of motion, the optimal subtraction of systematic signals, known within some amplitude and time shift, with the focus on measuring the noise provides an effective way to solve the problem and marginalize over nuisance parameters. The F statistic, in widespread use throughout the gravitation waves community, is included in the method and suitably generalized to marginalize over linear parameters and noise at the same time. The method is applied to LPF simulator data and, thanks to its generality, can also be applied to the data reduction and analysis of future gravitational wave detectors.

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

    International Nuclear Information System (INIS)

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

    1990-01-01

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

  4. Radiation-induced tritium labelling and product analysis

    Energy Technology Data Exchange (ETDEWEB)

    Peng, C.T. (California Univ., San Francisco, CA (United States). Dept. of Pharmaceutical Chemistry)

    1993-05-01

    By-products formed in radiation-induced tritium labelling are identified by co-chromatography with authentic samples or by structure prediction using a quantitative structure-retention index relationship. The by-products, formed from labelling of steroids, polynuclear aromatic hydrocarbons, 7-membered heterocyclic ring structures, 1,4-benzodiazepines, 1-haloalkanes, etc. with activated tritium and adsorbed tritium, are shown to be specifically labelled and anticipated products from known chemical reactions. From analyses of the by-products, one can conclude that the hydrogen abstraction by tritium atoms and the substitution by tritium ions are the mechanisms of labelling. Classification of the tritium labelling methods, on the basis of the type of tritium reagent, clearly shows the active role played by tritium atoms and ions in radiation-induced methods. (author).

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

    Energy Technology Data Exchange (ETDEWEB)

    Trivedi, A

    1994-06-01

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

  6. Impact of Center-of-Mass Acceleration on the Performance of Ultramarathon Runners

    Directory of Open Access Journals (Sweden)

    Lin Shun-Ping

    2014-12-01

    Full Text Available Ultramarathon races are rapidly gaining popularity in several countries, raising interest for the improvement of training programs. The aim of this study was to use a triaxial accelerometer to compare the three-dimensional centerof- mass accelerations of two groups of ultramarathon runners with distinct performances during different running speeds and distances. Ten runners who participated in the 12-h Taipei International Ultramarathon Race underwent laboratory treadmill testing one month later. They were divided into an elite group (EG; n = 5 and a sub-elite group (SG; n = 5. The triaxial center-of-mass acceleration recorded during a level-surface progressive intensity running protocol (3, 6, 8, 9, 10, and 12 km/h; 5 min each was used for correlation analyses with running distance during the ultramarathon. The EG showed negative correlations between mediolateral (ML acceleration (r = −0.83 to −0.93, p < 0.05, and between anterior-posterior (AP acceleration and running distance (r = −0.8953 to −0.9653, p < 0.05, but not for vertical control of the center of mass. This study suggests that runners reduce stride length to minimize mediolateral sway and the effects of braking on the trunk; moreover, cadence must be increased to reduce braking effects and enhance impetus. Consequently, the competition level of ultramarathons can be elevated.

  7. Tritium monitoring in environment at ICIT Tritium Separation Facility

    International Nuclear Information System (INIS)

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

    2008-01-01

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

  8. Development of the Accelerator Mass Spectrometry technology at the Comenius University in Bratislava

    Science.gov (United States)

    Povinec, Pavel P.; Masarik, Jozef; Ješkovský, Miroslav; Kaizer, Jakub; Šivo, Alexander; Breier, Robert; Pánik, Ján; Staníček, Jaroslav; Richtáriková, Marta; Zahoran, Miroslav; Zeman, Jakub

    2015-10-01

    An Accelerator Mass Spectrometry (AMS) laboratory has been established at the Centre for Nuclear and Accelerator Technologies (CENTA) at the Comenius University in Bratislava comprising of a MC-SNICS ion source, 3 MV Pelletron tandem accelerator, and an analyzer of accelerated ions. The preparation of targets for 14C and 129I AMS measurements is described in detail. The development of AMS techniques for potassium, uranium and thorium analysis in radiopure materials required for ultra-low background underground experiments is briefly mentioned.

  9. Tritium sources; Izvori tricijuma

    Energy Technology Data Exchange (ETDEWEB)

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

    1993-07-01

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

  10. Tritium inventory prediction in a CANDU plant

    International Nuclear Information System (INIS)

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

    1995-01-01

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

  11. Management of tritium at nuclear facilities

    International Nuclear Information System (INIS)

    1984-01-01

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

  12. Handling of tritium at TFTR

    International Nuclear Information System (INIS)

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

    1977-01-01

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

  13. 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.

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

    International Nuclear Information System (INIS)

    Bergman, C.; Wesslen, E.

    1977-01-01

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

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

    Energy Technology Data Exchange (ETDEWEB)

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

    1967-07-01

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

  16. Ion ratios and tritium extents as markers of salinization in the Bacolod City basin

    International Nuclear Information System (INIS)

    Castaneda, Soledad S.; Almoneda, Rosalina V.; Mendoza, Norman DS; Sucgang, Raymond J.

    2009-01-01

    Tritium statistics were used in tandem with geochemical information for the characterization of recharge to the Bacolod city basin. Waters were sampled from selected production wells,domestic wells, and surface water sources. The average tritium in the groundwater appeared to be 0.52 TU while surface and rain waters have an average of 0.86 and 0.89 TU, respectively. Physico-chemical properties (pH, conductivity, temperature) of the water were determined on site. Chemical characterization was focused on the determination of major ionic composition Na, K, Mg, Ca, as well as the major anions. Sulfate, (SO4), Chloride (Cl) by ion chromatography and bicarbonate ion by titration. Two portions of the basin displayed salient conductivity and chloride ion values which were strikingly greater than the rest f the other sampling points in the 3 year monitoring period. Tritium extents indicate that wells near the coasts receive potential contribution from modern recharge. Ion mass balance calculations and Br/Cl ratios corroborate tritium results to further validate that sea water intrusion may account for the high conductivities. The salinization and high conductivity of groundwater at points far from the coasts were attributed to connate formation at the deeper layer aquifers. Tritium extents indicated insignificant, sluggish recharge from precipitation before the 1950's, while ion mass balance do not indicate sea water intrusion. Establishment of geochemical data, in tandem with tritium, isotopic and other techniques, help in the identification of the origin and mechanism of recharge to the tapped aquifers which may aid local government units to properly delineate the areas that shall need concerted effort for protection, forest cover preservation and restoration within or outside the reservation area of the watershed. (author)

  17. Analysis of the organically bound tritium

    International Nuclear Information System (INIS)

    Baglan, N.; Alanic, G.

    2011-01-01

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

  18. A review of tritium licensing requirements

    International Nuclear Information System (INIS)

    Meikle, A.B.

    1982-12-01

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

  19. 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

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

    Energy Technology Data Exchange (ETDEWEB)

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

    2016-11-01

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

  1. Management of Tritium in ITER Waste

    International Nuclear Information System (INIS)

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

    2011-01-01

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

  2. Development of the Accelerator Mass Spectrometry technology at the Comenius University in Bratislava

    Energy Technology Data Exchange (ETDEWEB)

    Povinec, Pavel P., E-mail: povinec@fmph.uniba.sk; Masarik, Jozef; Ješkovský, Miroslav; Kaizer, Jakub; Šivo, Alexander; Breier, Robert; Pánik, Ján; Staníček, Jaroslav; Richtáriková, Marta; Zahoran, Miroslav; Zeman, Jakub

    2015-10-15

    An Accelerator Mass Spectrometry (AMS) laboratory has been established at the Centre for Nuclear and Accelerator Technologies (CENTA) at the Comenius University in Bratislava comprising of a MC-SNICS ion source, 3 MV Pelletron tandem accelerator, and an analyzer of accelerated ions. The preparation of targets for {sup 14}C and {sup 129}I AMS measurements is described in detail. The development of AMS techniques for potassium, uranium and thorium analysis in radiopure materials required for ultra-low background underground experiments is briefly mentioned.

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

    Energy Technology Data Exchange (ETDEWEB)

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

    2013-11-15

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

  4. Ultra-High Intensity Proton Accelerators and their Applications

    International Nuclear Information System (INIS)

    Weng, W. T.

    1997-01-01

    The science and technology of proton accelerators have progressed considerably in the past three decades. Three to four orders of magnitude increase in both peak intensity and average flux have made it possible to construct high intensity proton accelerators for modern applications, such as: spallation neutron sources, kaon factory, accelerator production of tritium, energy amplifier and muon collider drivers. The accelerator design focus switched over from intensity for synchrotrons, to brightness for colliders to halos for spallation sources. An overview of this tremendous progress in both accelerator science and technology is presented, with special emphasis on the new challenges of accelerator physics issues such as: H(-) injection, halo formation and reduction of losses

  5. Performance of the rebuilt SUERC single-stage accelerator mass spectrometer

    Science.gov (United States)

    Shanks, Richard P.; Ascough, Philippa L.; Dougans, Andrew; Gallacher, Paul; Gulliver, Pauline; Rood, Dylan H.; Xu, Sheng; Freeman, Stewart P. H. T.

    2015-10-01

    The SUERC bipolar single-stage accelerator mass spectrometer (SSAMS) has been dismantled and rebuilt to accommodate an additional rotatable pre-accelerator electrostatic spherical analyser (ESA) and a second ion source injector. This is for the attachment of an experimental positive-ion electron cyclotron resonance (ECR) ion source in addition to a Cs-sputter source. The ESA significantly suppresses oxygen interference to radiocarbon detection, and remaining measurement interference is now thought to be from 13C injected as 13CH molecule scattering off the plates of a second original pre-detector ESA.

  6. Tritium and plutonium in waters from the Bering and Chukchi Seas

    Science.gov (United States)

    Landa, E.R.; Beals, D.M.; Halverson, J.E.; Michel, R.L.; Cefus, G.R.

    1999-01-01

    During the summer of 1993, seawater in the Bering and Chukchi Seas was sampled on a joint Russian-American cruise [BERPAC] of the RV Okean to determine concentrations of tritium, 239Pu and 240Pu. Concentrations of tritium were determined by electrolytic enrichment and liquid scintilation counting. Tritium levels ranged up to 420 mBq L-1 showed no evidence of inputs other than those attribute atmospheric nuclear weapons testing. Plutonium was recovered from water samples by ferric hydroxide precipitation, and concentrations were determined by thermal ionization mass spectrometry. 239+240Pu concentrations ranged from nuclear facilities in the United States. This study and others sponsored by the International Atomic Energy Agency and the Office of Naval Research's Arctic Nuclear Waste Assessment Program are providing data for the assessment of potential radiological impacts in the Arctic regions associated with nuclear waste disposal by the former Soviet Union.

  7. Tritium pellet injector for TFTR

    International Nuclear Information System (INIS)

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

    1992-01-01

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

  8. Issues Associated with Tritium Legacy Materials

    International Nuclear Information System (INIS)

    Mills, Michael

    2008-01-01

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

  9. Analysis of in-pile tritium release experiments

    International Nuclear Information System (INIS)

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

    1992-01-01

    The objective of this work is to characterize tritium release behavior from lithium ceramics and develop insight into the underlying tritium release mechanisms. Analysis of tritium release data from recent laboratory experiments with lithium aluminate has identified physical processes which were previously unaccounted for in tritium release models. A new model that incorporates the recent data and provides for release from multiple sites rather than only one site was developed. Calculations of tritium release using this model are in excellent agreement with the tritium release behavior reported for the MOZART experiment

  10. CologneAMS, a dedicated center for accelerator mass spectrometry in Germany

    Energy Technology Data Exchange (ETDEWEB)

    Dewald, A., E-mail: dewald@ikp.uni-koeln.de [CologneAMS, Institute of Nuclear Physics, University of Cologne (Germany); Heinze, S.; Jolie, J.; Zilges, A. [CologneAMS, Institute of Nuclear Physics, University of Cologne (Germany); Dunai, T.; Rethemeyer, J.; Melles, M.; Staubwasser, M. [Institute of Geology and Mineralogy, University of Cologne (Germany); Kuczewski, B. [Division of Nuclear Chemistry, University of Cologne (Germany); Richter, J. [Institute of Prehistoric Archaeology, University of Cologne (Germany); Radtke, U. [Institute of Geography, University of Cologne, Germany, Rectorate, University of Duisburg-Essen (Germany); Blanckenburg, F. von [GFZ, German Research Centre for Geosciences, Potsdam (Germany); Klein, M. [HVEE, Amersfoort (Netherlands)

    2013-01-15

    CologneAMS is a new centre for accelerator mass spectrometry (AMS) at University of Cologne. It has been funded by the German Research Foundation (DFG) to improve the experimental conditions especially for those German scientists that apply the AMS technique for their geologic, environmental, nuclear chemical, and nuclear astrophysical research. The new AMS-device has been built by High Voltage Engineering Europe (HVEE) and has been installed in the existing accelerator area of the Institute of Nuclear Physics. The AMS-facility is designed for the spectrometry of {sup 10}Be, {sup 14}C, {sup 26}Al, {sup 36}Cl, {sup 41}Ca, {sup 129}I in and heavy ions up to {sup 236}U and {sup 244}Pu. The central part of the AMS-facility is a 6 MV Tandetron Trade-Mark-Sign accelerator. Downstream of the high energy mass spectrometer an additional switching magnet is used as a further filter element which supplies also additional ports for future extensions of the detector systems. The current status of CologneAMS and the results of the first test measurements will be presented.

  11. Analysis of tritium production in the vicinity of Linac and LEB tunnels at the Superconducting Super Collider Laboratory

    International Nuclear Information System (INIS)

    Nabelssi, B.K.

    1994-01-01

    Monte Carlo calculations were performed to estimate the tritium production in groundwater around the Linear Accelerator (Linac) and the Low Energy Booster (LEB) tunnels at the Superconducting Super Collider Laboratory (SSCL). The calculations were performed using the new version of the Los Alamos High Energy Transport (LAHET) code system (SUPERHET). Most of the tritium activity was found to occur in a zone extending 2 m from the tunnel wall. The calculated tritium production rate was used to derive the. maximum allowable beam losses that would result in an average groundwater concentration in the activation zone of 20 pCi/cm 3 , the federal maximum contaminant level (MCL) for tritium in drinking water. The maximum allowable beam losses were found to be about 4% and 2% of the maximum operating be.-un for the Linac at 1 GeV and the LEB at 11 GeV, resnectively. These percentages are well in excess of typical operational losses at existing highenergy accelerators. The results are in good agreement with previously reported calculations. Tritium saturation activity in water pipes resultina, from the derived maximum allowable beam loss was found to be 355 pCi/cm 3 in the Linac operating at 600 MeV and 363 pCi/cm 3 in the LEB operating at 11 GeV. Accidental tritium releases from water pipes were found to cause an inhalation dose rate of less than 0.013 (Linac at 600 MeV) and 0.009 mrem/hr (LEB at 11 Gev) in the tunnels. These dose rates are well within the laboratory's design limit of 0.1 mrem/hr for controlled areas. Accidental beam losses were found to cause activation in excess of the MCL only after an irradiation time of more than 557 hours in the Linac at 600 MeV and 69 hours in the LEB at 11 GeV. A full-beam accident lasting more than one hour is considered unlikely

  12. Calorimetric measurement of afterheat in target materials for the accelerator production of tritium

    International Nuclear Information System (INIS)

    Perry, R.B.

    1994-01-01

    The estimate of afterheat in a spallation target of lead (Pb) or tungsten (W), by calorimetry, is the purpose of this experiment in support of the Accelerator Production of Tritium (APT). Such measurements are needed to confirm code calculations, these being the only practical way of gaining this type of information in a form suitable to aid the design of the APT machine. Knowledge of the magnitude and duration of afterheat resulting from decay of activation products produced by proton bombardment of the target is necessary to quantify APT safety assumptions, to design target cooling and safety systems, and to reduce technical risk. Direct calorimetric measurement of the afterheat for the appropriate incident proton energies is more reliable than the available alternative, which is indirect, based on data from gamma-ray spectroscopy measurements. The basic concept, a direct measurement of decay afterheat which bypasses the laborious classical way of determining this quantity, has been demonstrated to work. The gamma-ray energy given off by the decay products produced in the activation of lead or tungsten with high-energy protons apparently does represent a significant fraction of the total decay energy. A calorimeter designed for measurement of isotopes decaying by alpha emission must be modified to reduce energy lost with escaping gamma rays. Replacement of the aluminum liner with a tungsten liner in the SSC measurement chamber resulted in a 270% increase in measured heat, proving that the energy loss in the earlier (1992) measurements was significant. Gamma-ray measurements are needed to confirm the gamma-ray absorption calculations for the calorimeter to determine the correction for loss of heat due to transmission of high-energy gamma rays through the calorimeter walls. The experiments at BLIP have shown that calorimetry can be a useful tool in measuring the afterheat in APT target materials

  13. 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

  14. 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

  15. Tritium behavior intentionally released in the room

    International Nuclear Information System (INIS)

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

    2008-01-01

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

  16. Accelerator mass spectrometry - Indian scenario. PD-1-1

    International Nuclear Information System (INIS)

    Kailas, S.

    2007-01-01

    Accelerator based ultra sensitive Mass Spectrometry (AMS) programmes are being vigorously pursued world over for the past three decades. There are more than 50 accelerator facilities devoted to this multidisciplinary activity. Realizing the importance of this programme, the work related to AMS has commenced at three major accelerator facilities in India: Institute of Physics, Bhubaneswar; Interuniversity Accelerator Centre, Delhi; BARC - TIFR Pelletron accelerator facility, Mumbai. At Bhubaneswar, facilities have been set up to carry our high precision 14 C based AMS programmes using the 3 MV Pelletron. A magnetic bouncer, an electrostatic analyzer and a chemistry lab for making samples in graphite form are some of the important features of this AMS facility. A number of users have already got their samples analysed using this AMS facility. The AMS programme has used upto 20 % of beam time available from the 3 MV Pelletron at Bhubaneswar. At Delhi efforts are underway and initial success has been achieved for carrying out 10 Be based AMS programme. Novel method based on simultaneously injecting oxide of Be - ( 9 Be and 17 O) and ( 10 Be and 16 O) has been tried to obtain the ratio of 9 Be / 10 Be. A velocity filter is also available for this programme. Both at Bhubaneswar and Delhi, provision exists in the form of a multi cathode target wheel for carrying out measurements for a number of samples. At Mumbai the emphasis has been in precision measurement of 36 Cl in samples. Segmented anode detector has been developed for the separation of interfering 36 S and 36 Cl isobars

  17. Overview of light sources powered by tritium

    International Nuclear Information System (INIS)

    Wu Jian; Lei Jiarong; Liu Wenke

    2012-01-01

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

  18. An integrated model of tritium transport and corrosion in Fluoride Salt-Cooled High-Temperature Reactors (FHRs) – Part I: Theory and benchmarking

    Energy Technology Data Exchange (ETDEWEB)

    Stempien, John D., E-mail: john.stempien@inl.gov; Ballinger, Ronald G., E-mail: hvymet@mit.edu; Forsberg, Charles W., E-mail: cforsber@mit.edu

    2016-12-15

    Highlights: • A model was developed for use with FHRs and benchmarked with experimental data. • Model results match results of tritium diffusion experiments. • Corrosion simulations show reasonable agreement with molten salt loop experiments. • This is the only existing model of tritium transport and corrosion in FHRs. • Model enables proposing and evaluating tritium control options in FHRs. - Abstract: The Fluoride Salt-Cooled High-Temperature Reactor (FHR) is a pebble bed nuclear reactor concept cooled by a liquid fluoride salt known as “flibe” ({sup 7}LiF-BeF{sub 2}). A model of TRITium Diffusion EvolutioN and Transport (TRIDENT) was developed for use with FHRs and benchmarked with experimental data. TRIDENT is the first model to integrate the effects of tritium production in the salt via neutron transmutation, with the effects of the chemical redox potential, tritium mass transfer, tritium diffusion through pipe walls, tritium uptake by graphite, selective chromium attack by tritium fluoride, and corrosion product mass transfer. While data from a forced-convection polythermal loop of molten salt containing tritium did not exist for comparison, TRIDENT calculations were compared to data from static salt diffusion tests in flibe and flinak (0.465LiF-0.115NaF-0.42KF) salts. In each case, TRIDENT matched the transient and steady-state behavior of these tritium diffusion experiments. The corrosion model in TRIDENT was compared against the natural convection flow-loop experiments at the Oak Ridge National Laboratory (ORNL) from the 1960s and early 1970s which used Molten Salt Reactor Experiment (MSRE) fuel-salt containing UF{sub 4}. Despite the lack of data required by TRIDENT for modeling the loops, some reasonable results were obtained. The TRIDENT corrosion rates follow the experimentally observed dependence on the square root of the product of the chromium solid-state diffusion coefficient with time. Additionally the TRIDENT model predicts mass

  19. Atmospheric tritium. Measurement and application

    International Nuclear Information System (INIS)

    Frejaville, Gerard

    1967-02-01

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

  20. Investigating Unsaturated Zone Travel Times with Tritium and Stable Isotopes

    Science.gov (United States)

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

    2017-12-01

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

  1. Measurement of tritium concentration in urine

    International Nuclear Information System (INIS)

    Sekiyama, Shigenobu; Deshimaru, Takehide

    1979-01-01

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

  2. Tritium-related materials problems in fusion reactors

    International Nuclear Information System (INIS)

    Hickman, R.G.

    1976-01-01

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

  3. Linear induction accelerator for heavy ions

    International Nuclear Information System (INIS)

    Keefe, D.

    1976-09-01

    There is considerable recent interest in the use of high energy (γ = 1.1), heavy (A greater than or equal to 100) ions to irradiate deuterium--tritium pellets in a reactor vessel to constitute a power source at the level of 1 GW or more. Various accelerator configurations involving storage rings have been suggested. A discussion is given of how the technology of Linear Induction Accelerators--well known to be matched to high current and short pulse length--may offer significant advantages for this application

  4. Tritium sorption by cement and subsequent release

    International Nuclear Information System (INIS)

    Ono, F.; Yamawaki, M.

    1995-01-01

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

  5. Tritium environmental transport studies at TFTR

    International Nuclear Information System (INIS)

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

    1993-01-01

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

  6. Tritium environmental transport studies at TFTR

    Science.gov (United States)

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

    1993-06-01

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

  7. Beta Decay in the Field of an Electromagnetic Wave and Experiments on Measuring the Neutrino Mass

    International Nuclear Information System (INIS)

    Dorofeev, O.F.; Lobanov, A.E.

    2005-01-01

    Investigations of the effect of an electromagnetic wave field on the beta-decay process are used to analyze the tritium-decay experimental data on the neutrino mass. It is shown that the electromagnetic wave can distort the beta spectrum, shifting the end point to the higher energy region. This phenomenon is purely classical and it is associated with the electron acceleration in the radiation field. Since strong magnetic fields exist in setups for precise measurement of the neutrino mass, the indicated field can appear owing to the synchrotron radiation mechanism. The phenomenon under consideration can explain the experimentally observed anomalies in the spectrum of the decay electrons; in particular, the effect of the 'negative square of the neutrino mass'

  8. Tritium system design studies of fusion experimental breeder

    International Nuclear Information System (INIS)

    Deng Baiquan; Huang Jinhua

    2003-01-01

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

  9. Use of tritium and helium-3 for oceanographic processes study. An example: the Northeastern Atlantic Ocean

    International Nuclear Information System (INIS)

    Andrie, C.; Merlivat, L.

    1987-01-01

    These results are relative to the TOPOGULF cruise during summer 1983. The sampled area is located near the Azores Islands on the both sides of the mid atlantic ridge. The tritium content of the surface waters reveals a strong front along the Azores current. At depth, the spatial distribution of tritium is studied along isopycnals. In the thermocline, it is essentially the anticyclonic gyre which is responsible for the northeast - southwest gradient in tritium concentration. Some informations about the age of the water masses are given by the use of both tritium and Helium-3. By this way are identified some areas where ventilation processes are active. At middepth, a strong contrast exists between the young waters originating from the Labrador Sea and the more stagnant waters in the South East of the sampled area

  10. Tritium in metals: Techniques of preparation

    International Nuclear Information System (INIS)

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

    1982-08-01

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

  11. Plasma Desorption Mass Spectrometry using TANDEM accelerator in National Industrial Research Inst. of Nagoya

    Energy Technology Data Exchange (ETDEWEB)

    Mizota, Takeshi; Nakao, Setsuo; Niwa, Hiroaki; Saito, Kazuo [Particle Beam Sceince Laboratory, Multi-Function Material Science Department, National Industrial Research Inst. of Nagoya, Nagoya (Japan)

    2001-02-01

    Plasma Desorption Mass Spectrometry (PDMS) analysis was studied using TANDEM accelerator. The heavy ions of MeV range emit the secondary ions of atoms, molecules, polymers and clusters from the irradiated samples without destruction. The analysis system of PDMS designed and set-up using a mass spectrometer of Time of Flight and the TANDEM accelerator. The system performance was tested for C-60 fullerene on the surface of the samples using 11.2 MeV {sup 28}Si beams produced by the TANDEM accelerator of 1.7MV. The result shows that the hydrogen and hydrocarbons can be analyzed in the range of 1amu unit. The resolution (M/{delta}M) of the Mass Spectrometry system is confirmed to be about 1000 from the separation of the 720 and 721amu peaks, which is attributed to the C-60 fullerene including {sup 13}C atoms. (H. Katsuta)

  12. Tritium research activities in Korea

    Energy Technology Data Exchange (ETDEWEB)

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

    2016-12-15

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

  13. Tritium metabolism in rat tissues

    International Nuclear Information System (INIS)

    Takeda, H.

    1982-01-01

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

  14. Radiation protection with consumer products containing gaseous tritium light sources; Strahlenschutz bei Konsumguetern mit Tritium-Gaslichtquellen

    Energy Technology Data Exchange (ETDEWEB)

    Rahders, Erio; Haeusler, Uwe [Bundesamt fuer Strahlenschutz, Berlin (Germany)

    2017-08-01

    Consumer products containing gaseous tritium light sources (GTLS) were examined with respect to their radiological safety potential regarding leak tightness or accidents. The maximum tritium leakage rate of 2.7 Bq/d determined from experimental testing is well below the criterion for leak tightness of sealed radioactive sources in DIN 25426-4. In order to investigate the incorporation of tritium due to contact with consumer products, 2 scenarios were reviewed; the correct use of a tritium watch and the accident scenario with a keyring.

  15. Mobility of Tritium in Engineered and Earth Materials at the NuMI Facility, Fermilab: Progress report for work performed between June 13 and September 30, 2006

    International Nuclear Information System (INIS)

    Pruess, Karsten; Conrad, Mark; Finsterle, Stefan; Kennedy, Mack; Kneafsey, Timothy; Salve, Rohit; Su, Grace; Zhou, Quanlin

    2006-01-01

    This report details the work done between June 13 and September 30, 2006 by Lawrence Berkeley National Laboratory (LBNL) scientists to assist Fermi National Accelerator Laboratory (Fermilab) staff in understanding tritium transport at the Neutrino at the Main Injector (NuMI) facility. As a byproduct of beamline operation, the facility produces (among other components) tritium in engineered materials and the surrounding rock formation. Once the tritium is generated, it may be contained at the source location, migrate to other regions within the facility, or be released to the environment

  16. 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)

  17. Tritium production and processing in a Tokamak reactor

    International Nuclear Information System (INIS)

    Leger, D.

    1986-09-01

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

  18. The organically bound tritium: an analyst vision

    International Nuclear Information System (INIS)

    Ansoborlo, E.; Baglan, N.

    2009-01-01

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

  19. Tritium Issues in Next Step Devices

    Energy Technology Data Exchange (ETDEWEB)

    C.H. Skinner; G. Federici

    2001-09-05

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

  20. Tritium Issues in Next Step Devices

    International Nuclear Information System (INIS)

    C.H. Skinner; G. Federici

    2001-01-01

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

  1. Accelerator mass spectrometry-enabled studies: current status and future prospects.

    Science.gov (United States)

    Arjomand, Ali

    2010-03-01

    Accelerator mass spectrometry is a detection platform with exceptional sensitivity compared with other bioanalytical platforms. Accelerator mass spectrometry (AMS) is widely used in archeology for radiocarbon dating applications. Early exploration of the biological and pharmaceutical applications of AMS began in the early 1990s. AMS has since demonstrated unique problem-solving ability in nutrition science, toxicology and pharmacology. AMS has also enabled the development of new applications, such as Phase 0 microdosing. Recent development of AMS-enabled applications has transformed this novelty research instrument to a valuable tool within the pharmaceutical industry. Although there is now greater awareness of AMS technology, recognition and appreciation of the range of AMS-enabled applications is still lacking, including study-design strategies. This review aims to provide further insight into the wide range of AMS-enabled applications. Examples of studies conducted over the past two decades will be presented, as well as prospects for the future of AMS.

  2. Modeling tritium transport in the environment

    International Nuclear Information System (INIS)

    Murphy, C.E. Jr.

    1986-01-01

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

  3. Tritium behavior in an aquatic ecosystem

    International Nuclear Information System (INIS)

    Komatsu, K.

    1982-01-01

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

  4. Tritium forms discrimination in ryegrass under constant tritium exposure: From seed germination to seedling autotrophy.

    Science.gov (United States)

    Renard, H; Maro, D; Le Dizès, S; Escobar-Gutiérrez, A; Voiseux, C; Solier, L; Hébert, D; Rozet, M; Cossonnet, C; Barillot, R

    2017-10-01

    Uncertainties remain regarding the fate of atmospheric tritium after it has been assimilated in grasslands (ryegrass) in the form of TFWT (Tissue Free Water Tritium) or OBT (Organically Bound Tritium). One such uncertainty relates to the tritium forms discrimination during transfer from TFWT to OBT resulting from photosynthesis (OBT photo ), corresponding to the OBT photo /TFWT ratio. In this study, the OBT/TFWT ratio is determined by experiments in the laboratory using a ryegrass model and hydroponic cultures, with constant activity of tritium in the form of tritiated water (denoted as HTO) in the "water" compartment (liquid HTO) and "air" compartment (HTO vapour in the air). The OBT photo /TFWT ratio and the exchangeable OBT fraction are measured for three parts of the plant: the leaf, seed and root. Plant growth is modelled using dehydrated biomass measurements taken over time in the laboratory and integrating physiological functions of the plant during the first ten days after germination. The results suggest that there is no measurable discrimination of tritium in the plant organic matter produced by photosynthesis. Copyright © 2017 Elsevier Ltd. All rights reserved.

  5. Tritium transport modeling at system level for the EUROfusion dual coolant lithium-lead breeding blanket

    Science.gov (United States)

    Urgorri, F. R.; Moreno, C.; Carella, E.; Rapisarda, D.; Fernández-Berceruelo, I.; Palermo, I.; Ibarra, A.

    2017-11-01

    The dual coolant lithium lead (DCLL) breeding blanket is one of the four breeder blanket concepts under consideration within the framework of EUROfusion consortium activities. The aim of this work is to develop a model that can dynamically track tritium concentrations and fluxes along each part of the DCLL blanket and the ancillary systems associated to it at any time. Because of tritium nature, the phenomena of diffusion, dissociation, recombination and solubilisation have been modeled in order to describe the interaction between the lead-lithium channels, the structural material, the flow channel inserts and the helium channels that are present in the breeding blanket. Results have been obtained for a pulsed generation scenario for DEMO. The tritium inventory in different parts of the blanket, the permeation rates from the breeder to the secondary coolant and the amount of tritium extracted from the lead-lithium loop have been computed. Results present an oscillating behavior around mean values. The obtained average permeation rate from the liquid metal to the helium is 1.66 mg h-1 while the mean tritium inventory in the whole system is 417 mg. Besides the reference case results, parametric studies of the lead-lithium mass flow rate, the tritium extraction efficiency and the tritium solubility in lead-lithium have been performed showing the reaction of the system to the variation of these parameters.

  6. Tritium extraction technologies and DEMO requirements

    Energy Technology Data Exchange (ETDEWEB)

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

    2016-11-01

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

  7. Tritium compatibility of alumina and Fosterite

    Energy Technology Data Exchange (ETDEWEB)

    Coffin, D.O.

    1979-09-01

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

  8. Disposal of tritium-exposed metal hydrides

    International Nuclear Information System (INIS)

    Nobile, A.; Motyka, T.

    1991-01-01

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

  9. The organic tritium in the environment

    International Nuclear Information System (INIS)

    Kirchmann, R.

    1979-01-01

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

  10. Tritium immobilisation

    International Nuclear Information System (INIS)

    Bridger, N.J.

    1982-01-01

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

  11. 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)

  12. Radionuclides in man and his environment measured by accelerator mass spectrometry

    International Nuclear Information System (INIS)

    Hellborg, Ragnar; Erlandsson, Bengt; Kiisk, Madis; Persson, Per; Skog, Goeran; Stenstroem, Kristina; Mattsson, Soeren; Leide-Svegborn, Sigrid; Olofsson, Mikael

    1999-01-01

    Accelerator mass spectrometry (AMS) is a highly sensitive analytical method for measuring very low concentrations of both radionuclides and stable nuclides. For radioanalytical purposes, the main advantages of AMS compared to conventional radiometric methods are the use of smaller samples (mg size) and shorter measuring times (less than one hour). In this report some current applications of the AMS technique at the Lund Pelletron accelerator are presented, in particular studies of 14 C-labeled pharmaceuticals used in clinical nuclear medicine and biomedical research

  13. Tritium behaviour in higher plants

    International Nuclear Information System (INIS)

    Guenot, J.

    1984-05-01

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

  14. 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

  15. Tritium practices past and present

    International Nuclear Information System (INIS)

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

    1980-01-01

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

  16. 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

  17. Transfer and incorporation of tritium in mammals

    International Nuclear Information System (INIS)

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

    1979-01-01

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

  18. Tritium safety issues for TFCX

    International Nuclear Information System (INIS)

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

    1985-01-01

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

  19. Risks of tritium and their mitigation

    International Nuclear Information System (INIS)

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

    1992-01-01

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

  20. Temporal sealing material of tritium-contaminated stainless steel

    International Nuclear Information System (INIS)

    Wen Wei; Dan Guiping; Zhang Dong; Qiu Yongmei; Zhang Li

    2010-01-01

    Tritium can be released from the exterior of tritium-contaminated stainless steel by slight stirring while decontaminating and disassembling. In order to avoid secondary tritium contamination to environment and operators, it is necessary to cover with an effective coating to tritium on the exterior of tritium-contaminated stainless steel and fill an effective substance to tritium inside. The results of tritium sealed experiments show that sealing efficiency of neutral silicone rubber is more than 85% for condition of static state and more than 99% for foam concrete condition of dynamic state. Neutral silicone rubber and foam concrete which have finer sealing efficiency can be used as temporal sealed material for the decontamination and disassembly of tritium-contaminated stainless steel. (authors)

  1. Accelerator mass spectrometry of small biological samples.

    Science.gov (United States)

    Salehpour, Mehran; Forsgard, Niklas; Possnert, Göran

    2008-12-01

    Accelerator mass spectrometry (AMS) is an ultra-sensitive technique for isotopic ratio measurements. In the biomedical field, AMS can be used to measure femtomolar concentrations of labeled drugs in body fluids, with direct applications in early drug development such as Microdosing. Likewise, the regenerative properties of cells which are of fundamental significance in stem-cell research can be determined with an accuracy of a few years by AMS analysis of human DNA. However, AMS nominally requires about 1 mg of carbon per sample which is not always available when dealing with specific body substances such as localized, organ-specific DNA samples. Consequently, it is of analytical interest to develop methods for the routine analysis of small samples in the range of a few tens of microg. We have used a 5 MV Pelletron tandem accelerator to study small biological samples using AMS. Different methods are presented and compared. A (12)C-carrier sample preparation method is described which is potentially more sensitive and less susceptible to contamination than the standard procedures.

  2. Tritium handling experience at Atomic Energy of Canada Limited

    Energy Technology Data Exchange (ETDEWEB)

    Suppiah, S.; McCrimmon, K.; Lalonde, S.; Ryland, D.; Boniface, H.; Muirhead, C.; Castillo, I. [Atomic Energy of Canad Limited - AECL, Chalk River Laboratories, Chalk River, ON (Canada)

    2015-03-15

    Canada has been a leader in tritium handling technologies as a result of the successful CANDU reactor technology used for power production. Over the last 50 to 60 years, capabilities have been established in tritium handling and tritium management in CANDU stations, tritium removal processes for heavy and light water, tritium measurement and monitoring, and understanding the effects of tritium on the environment. This paper outlines details of tritium-related work currently being carried out at Atomic Energy of Canada Limited (AECL). It concerns the CECE (Combined Electrolysis and Catalytic Exchange) process for detritiation, tritium-compatible electrolysers, tritium permeation studies, and tritium powered batteries. It is worth noting that AECL offers a Tritium Safe-Handling Course to national and international participants, the course is a mixture of classroom sessions and hands-on practical exercises. The expertise and facilities available at AECL is ready to address technological needs of nuclear fusion and next-generation nuclear fission reactors related to tritium handling and related issues.

  3. Torus evacuation and tritium handling on NET

    International Nuclear Information System (INIS)

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

    1986-08-01

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

  4. Tritium module for ITER/Tiber system code

    International Nuclear Information System (INIS)

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

    1988-01-01

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

  5. Storage and Assay of Tritium in STAR

    International Nuclear Information System (INIS)

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

    2005-01-01

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

  6. A method to quantify tritium inside waste drums: He{sup 3} ingrowth method

    Energy Technology Data Exchange (ETDEWEB)

    Godot, A.; Lepeytre, C.; Hubinois, J.C. [CEA Valduc, Dept. Traitement Materiaux Nucleaires, Service Analyses- Dechets, Lab. Chimie Analytique, 21 - Is-sur-Tille (France); Arseguel, A.; Daclin, J.P.; Douche, C. [CEA Valduc, Dept. Traitement Materiaux Nucleaires, Service Analyses- Dechets, Lab. de Gestion des Dechets Trities, 21 - Is-sur-Tille (France)

    2008-07-15

    This method enables an indirect, non intrusive and non destructive measurement of the Tritium activity in wastes drums. The amount of tritium enclosed inside a wastes drum can be determined by the measurement of the leak rate of {sup 3}He of this latter. The simulation predicts that a few months are necessary for establishing the equilibrium between the {sup 3}He production inside the drum and the {sup 3}He drum leak. In practice, after one year of storage, sampling {sup 3}He outside the drum can be realized by the mean of a confining chamber that collect the {sup 3}He outflow. The apparatus, the experimental procedure and the calculation of tritium activity from mass spectrometric {sup 3}He measurements are detailed. The industrial device based on a confinement cell and the automated process to measure the {sup 3}He amount at the initial time and after the confinement time is described. Firstly, reference drums containing a certified tritium activity (HTO) in addition to organic materials have been measured to qualify the method and to evaluate its performances. Secondly, tritium activity of organic wastes drums issued from the storage building in Valduc have been determined. Results of the qualification and optimised values of the experimental parameters are reported in order to determine the performances of this industrial device. As a conclusion, the apparatus enables the measurement of an activity as low as 1 GBq of tritium in a 200 liters drum containing organic wastes. (authors)

  7. Applications of proton and deuteron accelerators

    Energy Technology Data Exchange (ETDEWEB)

    Todd, A.M.M. (Grumman Corporate Research Center, Princeton, NJ (United States))

    1993-06-01

    Applications of positive and negative hydrogen and deuterium ion accelerators beyond basic research are increasing. Large scale proposed national laboratory/industrial projects include the Accelerator Production of Tritium (APT) which will utilize protons, and the International Fusion Material Irradiation Facility (IFMIF) which will accelerate a deuteron beam into a lithium target. At the small scale end, radio-frequency quadrupole (RFQ) accelerator based systems have been built for neutron activation analysis and for applications such as explosive detection. At an intermediate scale, the Loma Linda proton therapy accelerator is now successfully treating a full schedule of patients, and more than half a dozen such hospital based units are under active study world-wide. At this same scale, there are also several ongoing negative ion, military accelerator projects which include the Continuous Wave Deuterium Demonstrator (CWDD) and the Neutral Particle Beam Space Experiment (NPBSE). These respective deuterium and hydrogen accelerators, which have not been previously described, are the focus of this paper. (orig.)

  8. Automation system for tritium contaminated surface monitoring

    International Nuclear Information System (INIS)

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

    2005-01-01

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

  9. Study on tritium recovery from breeder materials

    International Nuclear Information System (INIS)

    Moriyama, H.; Moritani, K.

    1997-01-01

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

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

    International Nuclear Information System (INIS)

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

    2008-01-01

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

  11. 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

  12. Capture of Tritium Released from Cladding in the Zirconium Recycle Process

    Energy Technology Data Exchange (ETDEWEB)

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

    2016-08-31

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

  13. Capture of Tritium Released from Cladding in the Zirconium Recycle Process

    Energy Technology Data Exchange (ETDEWEB)

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

    2016-08-31

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

  14. 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

  15. 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.

  16. 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.

  17. A new tritium process monitor based on scintillating fibres

    International Nuclear Information System (INIS)

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

    1998-01-01

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

  18. Report of the consultants' meeting on accelerator mass spectrometry

    Energy Technology Data Exchange (ETDEWEB)

    NONE

    1995-07-01

    Accelerator Mass Spectrometry (AMS) has developed into a major analytical tool for the measurement of ultra-low-level long-lived radionuclides. Its use within the IAEA is recommended by the consultants in this meeting. The IAEA programs in which the technology would be useful and beneficial are: safeguards, physical and chemical sciences, human health, food and agriculture, radioactive waste management, radiation safety, industry and earth sciences.

  19. Report of the consultants' meeting on accelerator mass spectrometry

    International Nuclear Information System (INIS)

    1995-01-01

    Accelerator Mass Spectrometry (AMS) has developed into a major analytical tool for the measurement of ultra-low-level long-lived radionuclides. Its use within the IAEA is recommended by the consultants in this meeting. The IAEA programs in which the technology would be useful and beneficial are: safeguards, physical and chemical sciences, human health, food and agriculture, radioactive waste management, radiation safety, industry and earth sciences

  20. Tritium Removal from Carbon Plasma Facing Components

    International Nuclear Information System (INIS)

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

    2003-01-01

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

  1. 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

  2. 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.

  3. Radiocarbon dating with accelerator mass spectrometry

    International Nuclear Information System (INIS)

    Blake, W. Jr.

    1985-01-01

    Radiocarbon dating by means of accelerator mass spectrometry (AMS) has two great advantages over conventional dating: 1) much smaller samples can be handled and 2) counting time is significantly shorter. Three examples are given for Holocene-age material from east-central Ellesmere Island. The results demonstrate the potential use of this technique as a powerful research tool in studies of Quaternary chronology. Individual fragments of marine shells as small as 0.1 g have been dated successfully at the IsoTrace Laboratory, University of Toronto. In the case of an aquatic moss from a lake sediment core, an increment 0.5 cm thick could be used instead of a 5 cm-thick slice, thus allowing a much more precise estimate of the onset of organic sedimentation

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

    Science.gov (United States)

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

    2014-01-01

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

  5. Tritium effluent removal system

    International Nuclear Information System (INIS)

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

    1978-01-01

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

  6. TFTR tritium inventory accountability system

    International Nuclear Information System (INIS)

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

    1995-01-01

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

  7. Tritium management for fusion reactors

    International Nuclear Information System (INIS)

    Rouyer, J.L.; Djerassi, H.

    1985-01-01

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

  8. Radiotoxicity of tritium in mammals

    International Nuclear Information System (INIS)

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

    1972-12-01

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

  9. Environmental monitoring for tritium separation facility

    International Nuclear Information System (INIS)

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

    2001-01-01

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

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

    International Nuclear Information System (INIS)

    1978-01-01

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

  11. 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...

  12. Tritium migration studies at the Nevada Test Site

    International Nuclear Information System (INIS)

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

    1993-05-01

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

  13. Incorporation of tritium in milk lipids after feeding organically bound tritium to cows

    International Nuclear Information System (INIS)

    Rochalska, M.; Hoek, J. van den

    1982-01-01

    Hay labelled with organically bound tritium was given to two cows for a period of 26 to 28 days. During hay feeding and at different times thereafter, lipids (fatty acids, cholesterol, glycerol, choline phospholipids, other phospholipids, flycolipids and gangliosides) were isolated from milk fat, and their total and specific activities were determined. During tritium administration, fatty acids and cholesterol contained the highest total activity, but the specific activity was highest in cholesterol and choline phospholipids. Activity decreased most rapidly for fatty acids and cholesterol, so that at 56 and 182 days after termination of 3 H feedings, phospholipids and glycolipids made an important contribution to lipid activity in milk. Regression analysis of the values for tritium activity in milk fat samples after stopping tritium administration, showed that three components with different half lives could be distinguished. The differences in metabolic behaviour of the various lipids in milk fat are mainly concerned with their relative participation in these components. (author)

  14. 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.)

  15. Tritium sorption behavior on the percolation of tritiated water into a soil packed bed

    Energy Technology Data Exchange (ETDEWEB)

    Furuichi, Kazuya, E-mail: kfuruichi@aees.kyushu-u.ac.jp [Department of Advanced Energy Engineering, Kyushu University, 6-1, Kasuga-koen, Kasuga, Fukuoka 816-8580 (Japan); Katayama, Kazunari; Date, Hiroyuki [Department of Advanced Energy Engineering, Kyushu University, 6-1, Kasuga-koen, Kasuga, Fukuoka 816-8580 (Japan); Takeishi, Toshiharu [Factory of Engineering, Kyushu University, 744 Motooka Nishi-ku, Fukuoka 819-0395 (Japan); Fukada, Satoshi [Department of Advanced Energy Engineering, Kyushu University, 6-1, Kasuga-koen, Kasuga, Fukuoka 816-8580 (Japan)

    2016-11-01

    Highlights: • We establish the permeation model of tritiated water in the soil layer. • Saturated hydraulic conductivity of water in soil was gained by using the model. • The isotope exchange reaction coefficient was good agreement with experimental data. - Abstract: Development of tritium transport model in natural soil is an important issue from a viewpoint of safety of fusion reactors. The spill of a large amount of tritiated water to the environment is a concern accident because huge tritiated water is handled in a fusion plant. In this work, a simple tritium transport model was proposed based on the tritium transport model in porous materials. The overall mass transfer coefficient representing isotope exchange reaction between tritiated water and structural water in soil particles was obtained by numerically analyzing the result of the percolation experiment of tritiated water into the soil packed bed. Saturated hydraulic conductivity in the natural soil packed bed was obtained to be 0.033 mm/s. By using this value, the overall mass transfer capacity coefficients representing the isotope exchange reaction between tritiated water percolating through the packed bed and overall structural water on soil particles was determined to be 6.0 × 10{sup −4} 1/s. This value is much smaller than the mass transfer capacity coefficient between tritiated water vapor and water on concrete material and metals.

  16. Experiences with decontaminating tritium-handling apparatus

    International Nuclear Information System (INIS)

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

    1992-01-01

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

  17. 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.)

  18. Designing double-gap linear accelerators for a wide mass range

    International Nuclear Information System (INIS)

    Lysenko, W.P.; Wadlinger, E.A.; Rusnak, B.; Krawczyk, F.; Saadatmand, K.; Wan, Z.

    1998-01-01

    For applications like ion implantation, rf linacs using double-gap structures with external resonators can be used because they are practical at low frequencies. However, since the two gaps associated with a given resonator cannot be individually phased, it is not obvious how to build a linac that can efficiently accelerate particles having different mass/charge ratios. This paper describes the beam dynamics of double-gap rf linacs and shows how to maximize the range of mass/charge ratios. The theory also tells one how to rescale a linac tune (i.e., reset the voltages and phases) so that a new particle, having a different mass or charge, will behave similarly to the original particle

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

    International Nuclear Information System (INIS)

    Xie Yun; Shi Zhengkun; Wu Tao

    2014-01-01

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

  20. Tritium Management Loop Design Status

    Energy Technology Data Exchange (ETDEWEB)

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

    2017-12-01

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