Speciation of ¹²⁷I and ¹²⁹I in atmospheric aerosols at Risø, Denmark: insight into sources of iodine isotopes and their species transformations

DEFF Research Database (Denmark)

Zhang, Luyuan; Hou, Xiaolin; Xu, Sheng

2015-01-01

iodine have been determined for 129I and 127I in the aerosols collected at Risø, Denmark, between March and May 2011 (shortly after the Fukushima nuclear accident) and in December 2014. The measured concentrations of total iodine are in the range of 1.04–2.48 ng m−3 for 127I and (11.3–97.0) × 105 atoms m...... in the aerosols are found to be strongly related to their sources and atmospheric pathways. Aerosols that were transported over the contaminated ocean, contained higher amounts of 129I than aerosols transported over the European continent. The high 129I concentrations of the marine aerosols are attributed...... to secondary emission from heavily 129I-contaminated seawater rather than primary gaseous release from nuclear reprocessing plants. Water-soluble iodine was found to be a minor fraction to total iodine for both 127I (7.8–13.7 %) and 129I (6.5–14.1 %) in ocean-derived aerosols, but accounted for 20...

Large-scale input, inventories and transport of iodine-129 and iodine-127 in Germany. Final report; Grossflaechiger Eintrag, Inventare und Transport von Iod-129 und Iod-127 in Deutschland. Abschlussbericht

Energy Technology Data Exchange (ETDEWEB)

Riebe, Beate; Daraoui, Abdelouahed; Schwinger, Mareike

2014-03-15

Liquid and gaseous releases of {sup 129}I from European reprocessing plants result in a continuous accumulation in the environment. Aim of the project was to quantify the inventories and input and discharges of {sup 127}I and {sup 129}I of different environmental compartments all over Germany. Aerosol, rainwater and river water samples were collected continuously over a period of 2 years. Additionally, soil samples were collected at 30 different sampling sites. For {sup 127}I no correlation of concentration or deposition rates and distance of sampling sites from the North Sea was found for aerosol and precipitation samples, whereas the results for {sup 129}I showed decreasing values with increasing distance from the coast. Also for {sup 129}I inventories of soils a trend to decrease could be observed from the northern to the southern and from the western to the eastern part of the country. However, there is a close relationship between iodine and soil properties. Comparison of results with earlier investigations does not show a current increase of isotopic ratios and deposition rates. Thus, at present {sup 129}I concentrations and isotopic ratios do not pose the risk of an increased thyroid dose for the public.

The determination of iodine 129 in thyroids

International Nuclear Information System (INIS)

Gros, Roger; Cappellini, Liliane; Goujon de Beauvivier, Michel; Jeanmaire, Lucien; Patti, Francois.

1975-08-01

Activation analysis was used for the determination of 129 I in thyroids. Iodine is first extracted from the thyroid and irradiated as lead iodate, thus giving enough sensitivity and making it possible to use common laboratory material. The results showed that the present activity levels in France are between 1 and 50 pCi per gram of iodine; the values found in Argentina are clearly lower [fr

Iodine budget in surface waters from Atacama: Natural and anthropogenic iodine sources revealed by halogen geochemistry and iodine-129 isotopes

International Nuclear Information System (INIS)

Álvarez, Fernanda; Reich, Martin; Snyder, Glen; Pérez-Fodich, Alida; Muramatsu, Yasuyuki; Daniele, Linda; Fehn, Udo

2016-01-01

Iodine enrichment in the Atacama Desert of northern Chile is widespread and varies significantly between reservoirs, including nitrate-rich “caliche” soils, supergene Cu deposits and marine sedimentary rocks. Recent studies have suggested that groundwater has played a key role in the remobilization, transport and deposition of iodine in Atacama over scales of millions-of-years. However, and considering that natural waters are also anomalously enriched in iodine in the region, the relative source contributions of iodine in the waters and its extent of mixing remain unconstrained. In this study we provide new halogen data and isotopic ratios of iodine ("1"2"9I/I) in shallow seawater, rivers, salt lakes, cold and thermal spring water, rainwater and groundwater that help to constrain the relative influence of meteoric, marine and crustal sources in the Atacama waters. Iodine concentrations in surface and ground waters range between 0.35 μM and 26 μM in the Tarapacá region and between 0.25 μM and 48 μM in the Antofagasta region, and show strong enrichment when compared with seawater concentrations (I = ∼0.4 μM). In contrast, no bromine enrichment is detected (1.3–45.7 μM for Tarapacá and 1.7–87.4 μM for Antofagasta) relative to seawater (Br = ∼600 μM). These data, coupled to the high I/Cl and low Br/Cl ratios are indicative of an organic-rich sedimentary source (related with an “initial” fluid) that interacted with meteoric water to produce a mixed fluid, and preclude an exclusively seawater origin for iodine in Atacama natural waters. Iodine isotopic ratios ("1"2"9I/I) are consistent with halogen chemistry and confirm that most of the iodine present in natural waters derives from a deep initial fluid source (i.e., groundwater which has interacted with Jurassic marine basement), with variable influence of at least one atmospheric or meteoric source. Samples with the lowest isotopic ratios ("1"2"9I/I from ∼215 to ∼1000 × 10"�

Disposal of Iodine-129

International Nuclear Information System (INIS)

Morgan, M.T.; Moore, J.G.; Devaney, H.E.; Rogers, G.C.; Williams, C.; Newman, E.

1978-01-01

One of the problems to be solved in the nuclear waste management field is the disposal of radioactive iodine-129, which is one of the more volatile and long-lived fission products. Studies have shown that fission products can be fixed in concrete for permanent disposal. Current studies have demonstrated that practical cementitious grouts may contain up to 18% iodine as barium iodate. The waste disposal criterion is based on the fact that harmful effects to present or future generations can be avoided by isolation and/or dilution. Long-term isolation is effective in deep, dry repositories; however, since penetration by water is possible, although unlikely, release was calculated based on leach rates into water. Further considerations have indicated that sea disposal on or in the ocean floor may be a more acceptable alternative

Effects of radiation and impurities on gaseous iodine behavior in a containment vessel

International Nuclear Information System (INIS)

Takahashi, Masato; Watanabe, Atsushi; Hashimoto, Takashi

2000-01-01

In order to estimate the effect of impurities and radiation on gaseous iodine behavior in containment vessel, NUPEC has improved IMPAIR-3 code developed by PSI. Several modifications on the iodine oxidation by radiolysis and the production of nitric acid, the existence of boric acid, and the reaction of silver particle with iodine were newly added in evaluating the effect of radiolysis and impurities. pH change resulting from presence of boric acid, nitric acid production by radiolysis of air, and sodium hydroxide addition by AM operation, was also considered. The code verification for pH change was performed using the RTF experimental results. Additionally, the effects of boric acid and silver impurities on gaseous iodine behavior were evaluated by the sensitivity analysis. As a result, the experimental results of iodine concentration transient under pH change were well simulated. The following results were also obtained from the sensitive analysis. The gaseous iodine behavior was not affected by the existence of boric acid. In the case of silver existence in liquid phase, the gaseous iodine concentration rapidly decreased because a large amount of iodine changed into AgI species in liquid phase. The restraint effect of silver on gaseous iodine, production was larger than that of pH change. (author)

Iodine-129 and Iodine-127 speciation in groundwater at the Hanford Site, U.S.: iodate incorporation into calcite

International Nuclear Information System (INIS)

Zhang, Saijin; Yeager, Chris; Wellman, Dawn M.; Santschi, Peter H.

2013-01-01

The Hanford Site, the most contaminated nuclear site in the United States, has large radioactive waste plumes containing high 129I levels. The geochemical transport and fate of radioiodine depends largely on its chemical speciation that is greatly affected by environmental factors. This study reports, for the first time, the speciation of stable and radioactive iodine in the groundwater from the Hanford Site. Iodate was the dominant species and accounts for up to 84%, followed by organo-iodine and minimal levels of iodide. The relatively high pH and oxidizing environment may have prevented iodate reduction. Our results identified that calcite precipitation caused by degassing of CO2 during deep groundwater sampling incorporated between 7 to 40% of dissolved iodine (including 127I and 129I) that was originally in the groundwater, transforming dissolved to particulate iodate during sampling. In order to understand the mechanisms underlying iodine incorporation by calcite, laboratory experiments were carried out to replicate this iodine sequestering processes. Two methods were utilized in this study, 1) addition of sodium carbonate; 2) addition of calcium chloride followed by sodium carbonate where the pH was well controlled at ~8.2, which is close to the average pH of Hanford Site groundwater. It was demonstrated that iodate was the main species incorporated into calcite and this incorporation process could be impeded by elevated pH and decreasing ionic strength in groundwater. This study provides critical information for predicting the long-term fate and transport of 129I at the Hanford Site and reveals a potential means for improved remediation strategies of 129I

Tracing the Iodine-129 fallout in Argentina

Energy Technology Data Exchange (ETDEWEB)

Fernandez Niello, Jorge; Negri, Agustin; Arazi, Andres [Comision Nacional de Energia Atomica (CNEA), Buenos Aires (Argentina). Lab. TANDAR; Wallner, Anton [The Australian National University, Canberra (Australia). Dept. of Nuclear Physics; Niello, Jorge Fernandez [Universidad Nacional de San Martin, Campus Miguelete, Buenos Aires (Argentina)

2012-07-01

Full text: Long-lived {sup 129}I (half-life=15.6 Ma) is produced naturally by irradiation of atmospheric xenon by cosmic neutrons and in the sub-surface by spontaneous fission of {sup 238}U, from which the natural inventory of {sup 129}I has been estimated to be around 50,000 kg, only 140 kg of them corresponds to the hydrospheric inventory. Nuclear tests and accidents have added between 45-130 kg. Apart from a global atmospheric fallout component, {sup 129}I has been released from several nuclear fuel reprocessing plants located in the Northern Hemisphere (ca. 6000 kg) which serve as localized sources in oceanographic-tracer experiments. In this presentation, we report results from a study exploring the presence of {sup 129}I in the Southern Hemisphere by determining {sup 129}I/{sup 127}I isotopic ratios in water samples (rivers, lakes and shallow sea-water) taken at different latitudes in Argentina including Antarctica. The iodine-127 and iodine-129 concentrations were measured via ICP-MS (Inductively Coupled Plasma Mass Spectrometry) and Accelerator Mass Spectrometry (AMS), respectively. Distribution of both isotopes can be understood considering tropospheric circulation patterns, possible sources and regional precipitation patterns. Natural and anthropogenic sources for the Southern Hemisphere and their inventories are discussed. Similar contribution came from natural sources and nuclear tests. Contribution from the nuclear fuel reprocessing plants placed in the Northern hemisphere can be neglected. (author)

Long-lived Radionuclides in the Environment: On the Radioecology of Iodine-129

International Nuclear Information System (INIS)

Michel, R.; Klipsch, K.; Ernst, Th.; Vahlbruch, J.; Jakob, D.; Synal, H.A.; Schnabel, C.; Lopez-Gutierrez, J.M.

2004-01-01

Atmospheric nuclear weapons tests, nuclear accidents, and emissions from reprocessing plants have changed the natural abundances of the long-lived radionuclide 129 I (T 1/2 = 15.7 Ma) in a sustainable manner. But still today, the radioecology of 129 I is just incompletely known. In this paper, we summarize the results of a long-term project aimed on a comprehensive understanding of the abundances of 129 I and 127 I in Lower Saxony, Germany, and of their pathways through the different environmental compartments to man. To this end, accelerator mass spectrometry, radiochemical neutron activation analysis, ion chromatography, and ICP-MS were applied to measure the iodine isotopes in sea-water, air, precipitation, surface and ground waters, soils, plants, animals, foodstuffs, total diet, and human and animal thyroid glands. For air-borne iodine, the speciation as well as the particle size distribution of aerosols was determined. Soil depth profiles were investigated down to depths of 2.5 m in order to study the iodine migration as well as individual surface soil samples to allow for the determination of transfer factors of the iodine isotopes into plants. Also the transfer factors for feed-milk and feed-meat transfer were determined both for farm and wild animals. The iodine isotopes are in severe disequilibrium in the different environmental compartments. The pre-nuclear equilibrium 129 I/ 127 I ratio in the biosphere was determined to be 2.0 10 -13 with a geometric standard deviation of 1.39. Today, the environmental isotopic ratios in Northern Germany range from 10 -6 to 10 -10 . The highest ratios were found in North Sea water, the lowest in deep soil samples and ground water. The North Sea appears as the dominant source of air-borne iodine in Northern Germany due to the emissions of European reprocessing plants. A differentiation by about a factor of ten between the iodine isotopes was observed for the different air-borne species demonstrating the complexity of

Iodine-129 as a long-lived tracer in the environment

International Nuclear Information System (INIS)

Michel, R.; Ernst, T.; Szidat; Schnabel, C.; Synal, H.-A.

2002-01-01

129 I is an important tracer of human activities as well of environmental processes. However, its potential can only be exploited if the 129 I abundances in and the pathways between the different environmental compartments are known. Until today, our knowledge of the radioecology of 129 I is still insufficient. Results are presented from a long-term project which shall improve this situation. 129 I and 127 I abundances were investigated in precipitation, surface and ground waters from Lower Saxony, Germany, and in soil samples from various European locations. From the analysis of 129 I in rain, 129 I annual deposition densities were determined for the time period from 1997- 1999. We conclude that 129 I deposition rates in Switzerland and Germany increased by three orders of magnitude since 1950 and changed just little after 1987. The different 129 I/ 127 I ratios in precipitation, surface and ground waters allow to estimate mean residence times of iodine in surface soil zones. From the analysis of soils, 129 I deposition densities at various places of Europe were determined. Thereby, the 129 I natural equilibrium deposition density as well as that of the fall-out from atmospheric weapon tests was estimated. Elevated 129 I abundances in Ukrainian soils contaminated by Chernobyl fall-out provide a basis for retrospective dosimetry of the radiation exposure due to 131 I. Soil profiles from Germany exhibit the influence of ongoing emissions from European reprocessing plants and demonstrate the complexity of iodine migration. Biospheric 129 I/ 127 I ratios in Germany are an order of magnitude lower than in precipitation. Because of the disequilibrium of iodine isotopes in the different compartments further detailed investigations of the pathways of 129 I through the environment to man are considered necessary. (author)

Absorption of gaseous iodine by water droplets

International Nuclear Information System (INIS)

Albert, M.F.

1985-07-01

A new model has been developed for predicting the rate at which gaseous molecular iodine is absorbed by water sprays. The model is a quasi-steady state mass transfer model that includes the iodine hydrolysis reactions. The parameters of the model are spray drop size, initial concentration of the gas and liquid phases, temperature, pressure, buffered or unbuffered spray solution, spray flow rate, containment diameter and drop fall height. The results of the model were studied under many values of these parameters. Plots of concentration of iodine species in the drop versus time have been produced by varying the initial gas phase concentration of molecular iodine over the range of 1 x 10 -5 moles/liter to 1 x 10 -10 moles/liter and a drop size of 1000 microns. Results from the model are compared to results available from Containment Systems Experiments at Pacific Northwest Laboratory. The difference between the model predictions and the experimental data ranges from -120.5% to 68.0% with the closest agreement 7.7%. The new spray model is also compared to previously existing spray models. At high concentrations of gaseous molecular iodine, the new spray model is considered to be less accurate but at low concentrations, the new model predicts results that are closer to the experimental data than the model called the realistic model from WASH-1329. Inclusion of the iodine hydrolysis reaction is shown to be a feature important to a model intended for determining the removal of molecular iodine over a wide range of conditions

Measurement of Iodine-129 concentration in environmental water samples around Fukushima area - Role of river system in the global iodine cycle

Science.gov (United States)

Matsuzaki, Hiroyuki; Tokuyama, Hironori; Miyake, Yasuto; Honda, Maki; Yamagata, Takeyasu; Muramatsu, Yasuyuki

2013-04-01

According to Fukushima Dai-ichi Nuclear Power Plant (FDNPP) accident, vast amount of radioactive nuclides including radioactive iodine were spilled out into the environment. There is no question about that detailed observation of distribution of radioactive nuclides and evaluation of the radiation exposure of residents is extremely important. On the other hand, from the view of an elemental dynamics in the environment, this event can be considered as a spike of the radioactive isotope. It is also the case for the iodine. A rare isotope Iodine-129 was widely distributed in a very short time by the FDNPP accident. Iodine-129 directly landing on the soil surface had been trapped in the upper layer of the soil and the depth profile should indicate the migration in and the interaction with the soil. If Iodine-129 was trapped in the woods, it seems to take rather longer time to landing on the ground. Either way, a certain portion of the Iodine-129 should be moving downward and finally washed out by the groundwater or river with a certain rate and transported into the sea. The concentration of Iodine-129 in environmental water samples taken from rivers and ponds are considered to reflect the iodine transportation process by the fluvial system. For the detailed discussion of the role of the fluvial system in the global iodine cycle, Iodine-129 concentration of various water samples collected from Fukushima area was measured by means of Accelerator Mass Spectrometry. The results ranged from 3E06 atoms/L to 3E09 atoms/L. Samples from Abukuma area (South West of FDNPP) showed lower concentration. On the other hand, samples collected from North West part (Iitate village and Minami Soma region) showed higher concentration (more than 1E8 atoms/L). Delayed enhancement of Iodine-129 concentration over a year in river systems surrounded by woods was also observed which is considered to correspond to the delayed release from the woods.

Spatial distribution of Iodine-129 in surface soil around the Fukushima Daiichi Nuclear Power Plant

International Nuclear Information System (INIS)

Miyake, Yasuto; Tagi, Kazuhiro; Matsuzaki, Hiroyuki; Fujiwara, Takeshi; Saito, Takumi; Yamagata, Takeyasu; Tsuchiya, Yoko; Nakano, Chuichiro; Honda, Maki

2011-01-01

Due to the accident at the Fukushima Daiichi nuclear power plant, which was caused by the Great East Japan Earthquake, a lot of radioactive materials were released into the environment. Among them, Iodine-131, which has a short half-life of 8 days, is thought to be hardly detected after the accident is concluded. It is very important to research how leaked out Iodine-131 was diffused in order to estimate the health impact of radiation at the time of the accident. On the other hand, Iodine-129, which was leaked out and was thought to act chemically-identically as Iodine-131, has an extremely long half-life of 15.7 million years and we are able to measure it equally after the accident. By following the trail of Iodine-129, it is considered to estimate the distribution of Iodine-131. To do this, at first, it is essential to measure simultaneously Iodine-131 and Iodine-129 in the same sample picked from near-the Fukushima Daiichi nuclear power plant and examine the relation between them (for example, the isotopic ratio of Iodine derived from the nuclear power plant (I-129/I-131)). At this study, we measured Iodine-129 in surface soil within 60 kilometers of the Fukushima Daiichi nuclear power plant, which was picked by research team of Nuclear Engineering Research Laboratory, Faculty of Engineering, the University of Tokyo. We discuss Iodine-129 derived from the nuclear power plant by considering the concentration range, the relation of a distance or a direction from the nuclear power plant, and the relation between I-129 and other radioactive nuclides (Cs-134, Cs-137, I-131). Since Iodine-129, which had been leaked out from the nuclear fuel reprocessing plant in Europe, was already transferred to Japan by way of the atmospheric transportation before the accident, it is important to distinguish between Iodine-129 from this accident and from the reprocessing plant. Then, we want to obtain the I-129/I-131 ratio originating in the accident precisely and discuss the

Speciation of iodine (I-127 and I-129) in lake sediments

DEFF Research Database (Denmark)

Englund, E.; Aldahan, A.; Hou, Xiaolin

2010-01-01

Fallout of anthropogenic 129I at northern Europe has been occurring since the early 1950. Nevertheless, it is still unclear where and how this radioactive iodine is incorporated in the surface environment. In order to elucidate part of this problem, we here present an investigation of the occurre......Fallout of anthropogenic 129I at northern Europe has been occurring since the early 1950. Nevertheless, it is still unclear where and how this radioactive iodine is incorporated in the surface environment. In order to elucidate part of this problem, we here present an investigation...... the sediment. Organic bound iodine was the dominant form over other fractions, while iodine bound to metal oxides was negligible. The leachable part constituted 5–6% of the iodine. Diagenetic influence seems to exert a limited effect on distribution of iodine in the examined sediment section....

Methodology for iodine-129 determination in coniferous plant by neutron activation

International Nuclear Information System (INIS)

Quintana, E.E.; Thyssen, S.M.

1998-01-01

Full text: The measurement methods of iodine-129 ( 129 I) include liquid scintillation counting, mass spectrometry analysis, X-ray spectrometry and neutron activation analysis. The combination of long half-life and low radiation energy, limit the sensitivity of a direct measurement in environmental matrixes. The neutron activation analysis (NAA) permits the increase in the sensitivity because of the high thermal neutron cross section of 129 I. The reaction produced is 129 I (n,γ) 130 I and the Eγ (536 keV) of iodine-130 (t 1/2 = 12,6 hours) is measured. The developed methodology allows the determination of 129 I in coniferous needles using NAA. The chemical treatment removes the interferences present in the matrix, as well as the Bromine-82 originated in the activation process. The analytical method is divided in six steps: a) digestion by alkaline fusion; b) radiochemical purification of 129 I by distillation followed by solvent extraction; c) distillation and adsorption on activated charcoal; d) neutron irradiation; e) radiochemical purification of 130 I by distillation followed by solvent extraction; f) gamma spectrometry. Iodine-131 tracer is added, and a chemical recovery of 95% in the distillations is obtained. The whole process recovery is within 70% and 85%. The detection limit is 0.48 mBq. Several factors affect this value, such as sample type, variety of coniferous, natural iodine concentration, irradiation time and neutron flux. (author) [es

Iodine-129 AMS for Earth Science, Biomedical, and National Security Applications

International Nuclear Information System (INIS)

Nimz, G; Brown, T; Tumey, S; Marchetti, A; Vu, A

2007-01-01

This Laboratory Directed Research and Development project created the capability to analyze the radionuclide iodine-129 ( 129 I) by accelerator mass spectrometry (AMS) in the CAMS facility at LLNL, and enhanced our scientific foundation for its application through development of sample preparation technology required for environmental, biomedical, and national security applications. The project greatly improved our environmental iodine extraction and concentration methodology, and developed new techniques for the analysis of small quantities of 129 I. The project can be viewed as having two phases, one in which the basic instrumental and chemical extraction methods necessary for general 129 I analysis were developed, and a second in which these techniques were improved and new techniques were developed to enable broader and more sophisticated applications. The latter occurred through the mechanism of four subprojects that also serve as proof-of-principle demonstrations of our newly developed 129 I capabilities. The first subproject determined the vertical distribution of bomb-pulse 129 I ( 129 Iv distributed globally as fallout from 1950's atmospheric nuclear testing) through 5 meters in the upper vadose zone in the arid southwestern United States. This characterizes migration mechanisms of contaminant 129 I, or 129 I released by nuclear fuel reprocessing, as well as the migration of labile iodine in soils relative to moisture flux, permitting a determination of nutrient cycling. The second subproject minimized the amount of iodine required in an AMS sample target. Because natural iodine abundances are very low in almost all environments, many areas of research had been precluded or made extremely difficult by the demands of sample size. Also, certain sample types of potential interest to national security are intrinsically small - for example iodine on air filters. The result of this work is the ability to measure the 129 I/ 127 I ratio at the 2E-07 level or

Long-term migration of iodine in sedimentary rocks based on iodine speciation and 129I/127I ratio

Science.gov (United States)

Togo, Y.; Takahashi, Y.; Amano, Y.; Matsuzaki, H.; Suzuki, Y.; Muramatsu, Y.; Iwatsuki, T.

2012-12-01

[Introduction] 129I is one of the available indexes of long-term migration of groundwater solutes, because of its long half-life (15.7 million years) and low sorption characteristics. The Horonobe underground research center (Japan Atomic Energy Agency), at which are conducted research and development of fundamental techniques on geological disposal of high-level radioactive waste, is an appropriate site for natural analogue studies, because iodine concentration in groundwater is high in this area. To predict iodine behavior in natural systems, speciation of iodine is essential because of different mobility among each species. In this study, we determined iodine speciation and129I/127I isotope ratios of rock and groundwater samples to investigate long term migration of iodine. [Methods] All rock and groundwater samples were collected at Horonobe underground research center. The region is underlain mainly by Neogene to Quaternary marine sedimentary rocks, the Wakkanai Formation (Wk Fm, siliceous mudstones), and the overlying Koetoi Formation (Kt Fm, diatomaceous mudstones). Iodine species in rock samples were determined by iodine K-edge X-ray absorption near edge structure (SPring-8 BL01B1). Thin sections of rock samples were prepared, and iodine mapping were obtained by micro-XRF analysis (SPring-8 BL37XU). Iodine species (IO3-, I-, and organic I) in groundwater were separately detected by high performance liquid chromatography connected to ICP-MS. The 129I/127I ratios in groundwater and rock samples were measured by accelerator mass spectrometry (MALT, Univ. of Tokyo). Iodine in rock samples were separated by pyrohydrolysis and water extraction. [Results and discussion] Concentration of iodine in groundwater varied widely and was much higher than that of seawater showing a high correlation with that of chlorine (R2 = 0.90). Species of iodine in groundwater was mainly I-. Iodine in rock samples decreased near the boundary between Wk and Kt Fms. Iodine K-edge XANES

Iodine-129 in the environment

International Nuclear Information System (INIS)

Tikhomirov, F.A.; Moiseev, I.T.

1987-01-01

The quantitative ratio of aerial and soil entries of 129 I into plants, parameters of its migration in the system of atmosphere-soil-plants-river water, dynamics of transformation and biological availability of 129 I in soil for plants were studied on the basis of field observations and experiments using the radioactive tracers. The doses of human thyroid gland irradiation by 129 I under atmospheric and soil pathways of its transport into diet are estimated. 129 I content in soil due to its systematic, for 50 years, releases into atmosphere is shown to be negligible, agricultural production contamination by 129 I resulting mainly from its fallout onto overground phytomass. The period, needed to achieve 129 I concentration equilibrium in the atmosphere-soil system under constant average 129 I content in the air, varies depending on the soil type from several hundred years (for podzolic soils) up to several thousand years (for chernozem). The 129 I half-accumulation period is equal to 150 years for soddy-podzolic soil and to 700 years for chernozem. In case of 129 I fallout lasting for 100 years the annual increase of its content in overground phytomass due to the transport from soil will account for 0,3% of its atmospheric entry way for soddy-podzolic soil and for 0,1% for chernozem, respectively. For a number of sierozem, yellow soil and calcareous chernozem types this addition is higher (up to 1%). Under constant iodine-129 concentration in air (1 Bq/m3) the absorbed dose for one-year child's thyroid gland in continental area is approximately equal to 2 (Gy/y)/(Bq/m3). The absorbed dose from globally dissipated 129 I under 99% efficiency of gas purification will not exceed 2·10 -7 Gy/y. The input of globally dissipated 129 I, originating from deep underground disposal of nuclear wastes can account for not more than 10 -9 Gy/y. In total, 129 I releases for the coming century is not going to produce limitations for nuclear energetics development. (author)

Contribution to the study of gaseous molecular iodine washout by natural rains

International Nuclear Information System (INIS)

Fournier-Bidoz, V.

1991-01-01

This study is part of researches about nuclear accident prediction consequences on the environment. It concerns transfering of molecular gaseous iodine into liquids and especially precipitation scavenging below the cloud (washout). Bibliographic data directly concerned with this study (iodine's aqueous chemistry, aqueous to gaseous phases transfer) and also with its global frame-work (atmospheric release from a nuclear reactor in accidental situation and the behaviour of atmospheric iodine) are presented. Several experimental approaches have been performed in laboratory and on field. An aqueous to gaseous phase transfer simulator allowed us to isolate parameters involved in absorption and desorption of the halogen. Field experiments permit to quantify dry deposition on different solutions and to get a better insight of the phenomenon. Extrapolation of the whole results to precipitation scavenging of gaseous iodine I 2 by natural rains suggests that the process is an irreversible one. Washout rate values acquired during rainy experiments with molecular iodine emission or in a laboratory rainfall simulator agree with literatures data relative to irreversibility. However and even if reversibility was efficient it was not possible to clearly exhibit it according to experimental conditions. Moreover, the analytical iodine method which leads to a good experimental study has been presented

On-line measurement of gaseous iodine species during a PWR severe accident

Energy Technology Data Exchange (ETDEWEB)

Haykal, I.; Doizi, D. [CEA, DEN, Departement de Physico-chimie, 91191 Gif sur Yvette Cedex, (France); Perrin, A. [CNRS-University of Paris Est and Paris 7, Laboratoire Inter-Universitaire des Systemes Atmospheriques, 94010 Creteil, (France); Vincent, B. [University of Burgundy, Laboratoire de physique, CNRS UMR 5027, 9, Avenue Alain Savary, BP 47870, F-21078 Dijon Cedex, (France); Manceron, L. [Synchrotron SOLEIL, L' Orme des Merisiers, St-Aubin BP48, 91192 Gif-sur-Yvette Cedex, (France); Mejean, G. [University of Joseph Fourier in Grenoble, Laboratoire de Spectrometrie Physique-CNRS UMR 5588, 38402 Saint Martin d' Heres, (France); Ducros, G. [CEA Cadarache, CEA, DEN, Departement d' Etudes des Combustibles, 13108 Saint-Paul-lez-Durance cedex, (France)

2015-07-01

A long-range remote sensing of severe accidents in nuclear power plants can be obtained by monitoring the online emission of volatile fission products such as xenon, krypton, caesium and iodine. The nuclear accident in Fukushima was ranked at level 7 of the International Nuclear Event Scale by the NISA (Nuclear and Industrial Safety Agency) according to the importance of the radionuclide release and the off-site impact. Among volatile fission products, iodine species are of high concern, since they can be released under aerosols as well as gaseous forms. Four years after the Fukushima accident, the aerosol/gaseous partition is still not clear. Since the iodine gaseous forms are less efficiently trapped by the Filtered Containment Venting Systems than aerosol forms, it is of crucial importance to monitor them on-line during a nuclear accident, in order to improve the source term assessment in such a situation. Therefore, we propose to detect and quantify these iodine gaseous forms by the use of highly sensitive optical methods. (authors)

Method of removing iodine and compounds thereof from gaseous effluents

International Nuclear Information System (INIS)

Keener, R.L.; Kittle, P.A.

1976-01-01

Anion exchange resins including an acrylic backbone formed by the suspension polymerization of a mixture of an acrylic and a crosslinking monomer are useful in the removal of iodine and iodine compounds from gaseous effluents. Removal of radioactive iodine contaminants, particularly alkyl iodine compounds or hydrogen iodine, under extreme conditions, namely temperatures up to 180 0 C and humidities up to 100 percent, from effluents resulting from a major nuclear accident could probably be adsorbed by these resins described herein

Iodine-129 in rabbit thyroids near a nuclear fuel reprocessing plant in Idaho

International Nuclear Information System (INIS)

Fraley, L. Jr.; Bowman, G.C.; Markham, O.D.

1982-01-01

The 129 I/ 127 I atom ratios in rabbits collected on the INEL site were larger than ratios in rabbits from a control area. Maximum 129 I/ 127 I atom ratios (9.1 x 10 -4 ) occurred near the Idaho Chemical Processing Plant (ICPP). Based on rabbit thyroid concentrations, the 129 I appeared to be deposited primarily in the direction of the predominant winds from the ICPP, northeast and southwest. Dose rates from the 129 I to thyroids of INEL rabbits varied from 0.1 to 260 μGy/y (0.01 to 26 mrad/y). Iodine-129 atmospheric releases from the ICPP appeared to have increased the 129 I/ 127 I atom ratios on and near the INEL site. (author)

Measurement of Iodine-129 in surface soil collected near the Fukushima Daiichi nuclear power plant accident site

International Nuclear Information System (INIS)

Miyake, Yasuto; Matsuzaki, Hiroyuki; Fujiwara, Takeshi; Saito, Takumi; Yamagata, Takeyasu; Honda, Maki

2013-01-01

Iodine-129 in soil around Fukushima Daiichi nuclear power plant were measured by Accelerator Mass Spectrometry and isotopic ratio of radioiodine was estimated. Surface deposition amount of Iodine-129 resulted in 6.7 to 5500 mBq/m"2. The mean isotopic ratio between Iodine-129 and Iodine-131 at the accident was estimated that "1"2"9"I"/"1"3"1I = 26±6 as of March 11 2011. This result was compared to the calculation result of ORIGEN2 code to test the validity of this estimation. (author)

Methods of iodine-129 analysis for environmental monitoring

International Nuclear Information System (INIS)

Yamato, Aiji; Miyagawa, Naoto; Nomura, Tamotsu; Kinoshita, Mutsumi

1976-01-01

Some methods for the analysis of I-129 in the environment are described. Iodide ion in seawater is coprecipitated with chloride ion by silver citrate powder, and that in seaweeds and in sediment is sublimated by heating at about 900 0 C in O 2 atmosphere, and then the iodine is trapped in cooled NaOH and NaHSO 3 mixed solution. The trapped iodine is precipitated with AgNO 3 solution for γ-/X-ray spectrometry (detection limit asymptotically equals 30 pCi), or extracted into toluene scintillater solution for liquid scintillation counting. The decomposition of AgI is necessary for low level I-129 measurement; The AgI was transfered in a flask, added with 2N H 2 SO 4 and Zn sand, and decomposed by stirring for 2 hr. Filtered the solution, added 0.5 g of NaNO 2 and toluene scintillater to extract the iodine then added 1 ml of 2-methyl 1-butene to decolorize, the solution is measured by a liquid scintillation counter (detection limit asymptotically equals 1 pCi). This method can be applied for monitoring of low level radioactive water waste. (auth.)

Radioactivity of French coast of the Channel due to the release of technectium 99 and iodine 129: modelisation and measurements

International Nuclear Information System (INIS)

Robeau, D.; Patti, F.; Charmasson, S.

1988-01-01

Radioactive releases of Iodine 129 are controlled by measurements of the radioactivity in the liquid effluents before it is released in to the sea from the outlet of the reprocessing plant of La Hague. The effects on the marine environment are examined by a radioactive survey of Technecium 99 and Iodine 129 in Fucus (common seaweed). This radioactivity is measured along the north coast of France from Roscoff in the west of Brittany to Wimereux close to the Belgian frontier. The theoretical study of dispersion of radionuclides in the Channel has permitted a simulation model of the transfer of pollutants and particularly Technecium 99 and Iodine 129 to be formulated. (author)

The iodine reactivity

International Nuclear Information System (INIS)

2003-01-01

The iodine is an important element because it has long life isotopes (such as iodine 129) and a great mobility in natural media. Iodine presents a complex chemistry because of its volatility and its strong redox reactivity. The S.E.C.R. works to better understand the reactivity of this element in different natural, industrial or biological environments. It plays a part in thermochemical sites as a possible way of hydrogen formation. This seminar gives some aspects relative to the chemical reactivity of iodine, since its thermochemistry in the I/S cycles to produce hydrogen to its reactivity in the natural medium and its potential radiological impact. This document includes 4 presentations transparencies) dealing with: the 129 I cycle rejected in the low radioactive gaseous and liquid effluents of the La Hague reprocessing plant (C. Frechou); a bibliographic review of iodine retention in soils (F. Bazer-Bachi); the hydrogen production and the iodine/sulfur thermochemical cycle (role of iodine in the process); and the direct characterization by electro-spray ionization mass spectroscopy of iodine fixation by fulvic acids (P. Reiller, B. Amekraz, C. Moulin, V. Moulin)

Transfer of gaseous iodine from atmosphere to rough rice, brown rice and polished rice

International Nuclear Information System (INIS)

Sumiya, Misako; Uchida, Shigeo; Muramatsu, Yasuyuki; Ohmomo, Yoichiro; Yamaguchi, Shuho; Obata, Hitoshi.

1987-01-01

Experiments were carried out in order to obtain information required for establishing transfer coefficients of gaseous iodine (I 2 ) to rough rice, brown rice and polished rice. The gaseous iodine deposited on young rice plants before the heading period was scarcely found in the rough rice harvested at the full ripe stage. The biological half life of iodine in hull, however, was much slower than that in leaves of 14 days. The translocation of iodine from leaves and stalks to rough rice was not clearly recognized. Therefore, it was deduced that iodine found in brown rice mainly should originate from that deposited on the hull. The distribution ratios of iodine between rough rice and brown rice, and between brown rice and polished rice were 100:4 and 100:30 on 100 grains basis, respectively. If average normalized deposition velocity (V d(m) ) or derived deposition velocity (V s ) are given, the transfer coefficients of gaseous iodine to rough rice (TF r ), brown rice (TF b ) and polished rice (TF p ) could be calculated. (author)

Contamination of North Sea and Baltic Sea with long-living iodine-129 and other anthropogenic radionuclides; Kontamination von Nord- und Ostsee mit langlebigem Iod-129 und anderen anthropogenen Radionukliden

Energy Technology Data Exchange (ETDEWEB)

Tosch, Luebbert

2010-10-12

The radionuclide iodine-129 (T{sub 1/2} = 15.7 Ma) is produced in nature by spontaneous fission of uranium-238 and by cosmic ray induced spallation of xenon. Due to the military and civil use of neutron-induced fission of uranium-235 and plutonium-239 a huge amount of iodine-129 has been released into the environment. The main sources of anthropogenic {sup 129}I are the reprocessing plants in La Hague (France) near the English Channel and in Sellafield (UK) close to the Irish Sea. The natural equilibrium {sup 129}I/{sup 127}I-isotopic ratios are estimated to 1.5 . 10{sup -12} for the marine hydrosphere and to 3.0 . 10{sup -13} for the terrestrial biosphere respectively. Due to the emissions of anthropogenic iodine-129 the {sup 129}I/{sup 127}I-isotopic ratios have been increased in all compartments of the environment. Surface water samples taken from the English Channel, the North Sea, the Baltic Sea, the Irish Sea, and the North Atlantic give information about anthropogenic changes. Iodine turns out to be a conservative tracer in seawater. The iodine-127 concentrations in seawater except for coastal areas are rather constant (40.7 ± 6.2 ng/g). The observed {sup 129}I/{sup 127}I-isotopic ratios range between 10{sup -10} and more than 10{sup -6}. The variation of the {sup 129}I/{sup 127}I-isotopic ratios is caused by the admixture of anthropogenic iodine-129. Water samples taken far away from the reprocessing plants show the lowest isotopic ratios. The highest {sup 129}I/{sup 127}I-isotopic ratios are found near the reprocessing plants. The transport of {sup 129}I from La Hague has a rather clear pattern. It can be observed along the coasts of France, Belgium, the Netherlands, Germany and Denmark. The iodine-129 emissions from Sellafield can be followed northbound along the Scottish coast. The results of other anthropogenic radionuclides are used for discussing transport processes in the North Sea and the Irish Sea. Large areas in the North Sea are characterised by

The behavior of gaseous iodine in sand

International Nuclear Information System (INIS)

Takahashi, Kanji

1974-01-01

Radioactive iodine gas was passed through 10 different sands collected at rivers and hills. The relation between the amount of the loaded gas and the amount of adsorbed gas was determined at room temperature, 50 -- 60 0 C, and 90 -- 100 0 C under humidity of 2 sand. This amount was about 1 -- 3 times as much as that of monomolecular membrane adsorption, 0.2 -- 0.3 μg/cm 2 . The decrease of adsorption amount that accompanies the increase of humidity is attributable to the decrease of effective surface area of sand due to the presence of water. The transport of iodine in sand was studied by passing gaseous iodine through a glass tubing packed with sand. The distribution in the flow direction of iodine indicated that the ease of desorption depends upon the situation of adsorption. Easily desorbed case was named Henry type adsorption. Hardly desorbed case was named absorption type. Discussion is made on experimental results. (Fukutomi, T.)

Iodine Gas Trapping using Granular Porous Bismuth

Energy Technology Data Exchange (ETDEWEB)

Yang, Jae Hwan; Shin, Jin Myeong; Park, Jang Jin; Park, Geun Il [Korea Atomic Energy Research Institute, Daejeon (Korea, Republic of); Yim, Mansung [Korea Advanced Institute of Science and Technology, Daejeon (Korea, Republic of)

2014-05-15

{sup 129}I is a radionuclide with a very long half-life of 1.57 Χ 10{sup 7} years and has negative health effects to the human body. Therefore, the emission of {sup 129}I into the air is closely regulated by the Environmental Protection Agency (EPA). Many methods for trapping gaseous {sup 129}I have been developed thus far, including wet scrubbing and adsorption using silver loaded zeolites. Although wet scrubbing can effectively remove iodine, it suffers from corrosion of the vessel due to high concentration of the scrubbing solution. Silver loaded zeolites also show effectiveness in capturing {sup 129}I gas, yet weak thermal stability of physisorbed iodine remains a challenge. We studied a novel and facile method to trap iodine gas using bismuth. Granular bismuth having many pores was synthesized using bismuth nitrate and polyvinyl alcohol as a bismuth precursor and pore forming agent, respectively. Reaction of iodine and our samples resulted in an iodine capturing capacity of more than 2 times that of the commercial grade silver exchanged zeolite (AgX). Granular porous bismuths synthesized using bismuth nitrate and PVA show a promising performance in capturing iodine gas. The use of bismuth in trapping {sup 129}I gas can reduce the process cost as bismuth is cheap. Further study is going on to improve the mechanical property of granular porous bismuths for their easy handling.

Iodine Gas Trapping using Granular Porous Bismuth

International Nuclear Information System (INIS)

Yang, Jae Hwan; Shin, Jin Myeong; Park, Jang Jin; Park, Geun Il; Yim, Mansung

2014-01-01

129 I is a radionuclide with a very long half-life of 1.57 Χ 10 7 years and has negative health effects to the human body. Therefore, the emission of 129 I into the air is closely regulated by the Environmental Protection Agency (EPA). Many methods for trapping gaseous 129 I have been developed thus far, including wet scrubbing and adsorption using silver loaded zeolites. Although wet scrubbing can effectively remove iodine, it suffers from corrosion of the vessel due to high concentration of the scrubbing solution. Silver loaded zeolites also show effectiveness in capturing 129 I gas, yet weak thermal stability of physisorbed iodine remains a challenge. We studied a novel and facile method to trap iodine gas using bismuth. Granular bismuth having many pores was synthesized using bismuth nitrate and polyvinyl alcohol as a bismuth precursor and pore forming agent, respectively. Reaction of iodine and our samples resulted in an iodine capturing capacity of more than 2 times that of the commercial grade silver exchanged zeolite (AgX). Granular porous bismuths synthesized using bismuth nitrate and PVA show a promising performance in capturing iodine gas. The use of bismuth in trapping 129 I gas can reduce the process cost as bismuth is cheap. Further study is going on to improve the mechanical property of granular porous bismuths for their easy handling

Iodine-129 dose to the world population from the nuclear power industry

International Nuclear Information System (INIS)

Kocher, D.C.; Till, J.E.

1979-01-01

Because of the 15.7 million-year half life for 129 I and the mobility of iodine in the environment, releases of 129 I result in potential radiological impacts on the entire world population essentially in perpetuity. This paper presents estimates of dose to the world population from releases of 129 I by the world nuclear power industry during the years 1975 to 2020

A global-scale dispersion analysis of iodine-129 from nuclear fuel reprocessing plants

International Nuclear Information System (INIS)

Nishizawa, Masato; Suzuki, Takashi; Nagai, Haruyasu; Togawa, Orihiko

2010-01-01

A three-dimensional global chemical transport model, MOZART-2, is applied to investigate the global-sale dispersion of Iodine-129 from nuclear fuel reprocessing plants. The concentration and deposition of 129 I obtained by MOZART-2 are dispersed all over the Northern Hemisphere. The emission of 129 I to the atmosphere is thus important in considering the transport of 129 I to remote sites. (author)

Iodine-129 in Seawater Offshore Fukushima: distribution, inorganic speciation, sources, and budget

DEFF Research Database (Denmark)

Hou, Xiaolin; Povinec, Pavel P.; Zhang, Luyuan

2013-01-01

The Fukushima nuclear accident in March 2011 has released a large amount of radioactive pollutants to the environment. Of the pollutants, iodine-129 is a long-lived radionuclide and will remain in the environment for millions of years. This work first report levels and inorganic speciation of 129...

Standard guide for the determination of iodine-129 In uranium oxide

CERN Document Server

American Society for Testing and Materials. Philadelphia

2006-01-01

1.1 This method covers the determination of iodine-129 (129I) in uranium oxide by gamma-ray spectrometry. The method could also be applicable to the determination of 129I in aqueous matrices. 1.2 This standard does not purport to address all of the safety concerns, if any, associated with its use. It is the responsibility of the user of this standard to establish appropriate safety and health practices and to determine the applicability of regulatory limitations prior to use.

Distribution of {sup 129}I in terrestrial surface water environments

Energy Technology Data Exchange (ETDEWEB)

Chen, Xuegao [State Key Laboratory of Hydrology-Water Resources and Hydraulic Engineering, Hohai University, Nanjing 210098 (China); College of Hydrology and Water Resources, Hohai University, Nanjing (China); Gong, Meng [College of Hydrology and Water Resources, Hohai University, Nanjing (China); Yi, Peng, E-mail: pengyi1915@163.com [State Key Laboratory of Hydrology-Water Resources and Hydraulic Engineering, Hohai University, Nanjing 210098 (China); College of Hydrology and Water Resources, Hohai University, Nanjing (China); Aldahan, Ala [Department of Earth Sciences, Uppsala University, Uppsala (Sweden); Department of Geology, United Arab Emirates University, Al Ain (United Arab Emirates); Yu, Zhongbo [State Key Laboratory of Hydrology-Water Resources and Hydraulic Engineering, Hohai University, Nanjing 210098 (China); College of Hydrology and Water Resources, Hohai University, Nanjing (China); Possnert, Göran [Tandem Laboratory, Uppsala University, Uppsala (Sweden); Chen, Li [State Key Laboratory of Hydrology-Water Resources and Hydraulic Engineering, Hohai University, Nanjing 210098 (China); College of Hydrology and Water Resources, Hohai University, Nanjing (China)

2015-10-15

The global distribution of the radioactive isotope iodine-129 in surface waters (lakes and rivers) is presented here and compared with the atmospheric deposition and distribution in surface marine waters. The results indicate relatively high concentrations in surface water systems in close vicinity of the anthropogenic release sources as well as in parts of Western Europe, North America and Central Asia. {sup 129}I level is generally higher in the terrestrial surface water of the Northern hemisphere compared to the southern hemisphere. The highest values of {sup 129}I appear around 50°N and 40°S in the northern and southern hemisphere, separately. Direct gaseous and marine atmospheric emissions are the most likely avenues for the transport of {sup 129}I from the sources to the terrestrial surface waters. To apply iodine-129 as process tracer in terrestrial surface water environment, more data are needed on {sup 129}I distribution patterns both locally and globally.

Translocation of iodine-129 in soil and transfer to vegetation

International Nuclear Information System (INIS)

Handl, J.

1989-01-01

The translocation of I-129 in the soil and its long-term transfer from soil to plant have been investigated using an undisturbed soil column and a pasture on a river bank. The I-129 profiles in the soils of the monolith and the pasture exhibit clear differences in the distribution of radioiodine after 52 and 47 months, respectively. At those times after surface contamination of both soil types 88% (monolith) and 66% (pasture) of the total I-129 activity were found in the top soil layer of 10 cm, indicating that translocation in the pasture soil is faster than in the monolith. Apart from soil-specific parameters this behaviour may be explained by anaerobic conditions created in the soil due to high water levels in the nearby river attecting the chemical form of iodine. The distribution of stable iodine was found rather homogeneous in both soils with mean contents of 3 mg I-127 kg -1 d.w. in the upper 15 cm and 4 mg I-127 kg -1 d.w. in deeper layers in case of the monolith. For the pasture soil the corresponding values are about 4 and 5 mg I-127 kg -1 d.w. Transfer factors plant/soil (dry weight basis) of I-129 obtained from the monolith 39 g and 52 months after contamination are 1.5x10 -3 and 2.1x10 -3 , respectively. Data from the pasture 35 and 47 months after contamination show values of 9.0x10 -3 and 8.4x10 -3 , respectively. Transfer factors of stable iodine are significantly higher in both soils yielding an average value of 1.0 for the monolith and 0.3 for the pasture. Delay constants (related to a top soil layer of 10 cm) calculated for I-129 using data obtained from the long-term translocation processes to deeper soil layers in the monolith and in the pasture show values of 1x10 -9 s -1 and 4x10 -9 s -1 , respectively. (orig.) [de

Derivation of radioecological parameters from the long-term emission of iodine-129. Final report

International Nuclear Information System (INIS)

Michel, R.; Klipsch, K.; Ernst, T.; Gorny, M.; Jakob, D.; Vahlbruch, J.; Synal, H.A.; Schnabel, C.

2004-01-01

In this project, the distribution and behaviour of 129 I and 127 I in the environment and its pathways through the environment to man were comprehensively investigated in order to provide a basis for estimating the radiation exposure to man due to releases of 129 I. To this end, the actual situation in Lower Saxony, Germany, was studied for exemplary regions near to and far from the coast of the North Sea. Accelerator mass spectrometry, radiochemical neutron activation analysis, ion chromatography, and ICP-MS were applied to measure the iodine isotopes, 129 I and P 127 I, in sea-water, air, precipitation, surface and ground waters, soils, plants, animals, foodstuffs, total diet, and human and animal thyroid glands. For air-borne iodine, the speciation as well as the particle size distribution of aerosols was determined. Soil depth profiles were investigated down to depths of 2.5 m in order to study the iodine migration as well as individual surface soil samples to allow for the determination of transfer factors of the iodine isotopes into plants. From the analytical results radioecological parameters for the long-term behaviour of 129 I in the pedo- and biosphere were derived. The iodine isotopes are in severe disequilibrium in the different environmental compartments. The pre-nuclear equilibrium 129 I/ 127 I ratio in the biosphere was determined to be 2.0 x 10 -13 with a geometric standard deviation of 1.39. Today, the environmental isotopic ratios in Northern Germany range from 10 -6 to 10 -10 . The highest ratios are found in North Sea water, the lowest in deep soil samples and ground water. The North Sea appears as the dominant source of air-borne iodine in Northern Germany due to the emissions of European reprocessing plants. The results are discussed with respect to their radiological relevance and in view of the general protection of the environment, i.e. air, water, soil and the biosphere. (orig.)

Development of a coupled diffusion denuder system combined with gas chromatography/mass spectrometry for the separation and quantification of molecular iodine and the activated iodine compounds iodine monochloride and hypoiodous acid in the marine atmosphere.

Science.gov (United States)

Huang, Ru-Jin; Hoffmann, Thorsten

2009-03-01

This study concerns the development of a coupled diffusion denuder system capable of separating and quantifying gaseous molecular iodine (I(2)) and two other highly reactive iodine species, ICl and HOI, which are collectively named activated iodine compounds (AIC). Both I(2) and AIC are key species in the atmospheric chemistry of iodine. 1,3,5-Trimethoxybenzene (1,3,5-TMB)- and alpha-cyclodextrin/(129)I(-) (alpha-CD/(129)I(-))-coated denuders proved to be suitable for the collection of gaseous AIC and I(2), respectively. The experimental collection efficiencies for AIC (tested as ICl) and I(2) agreed well with the theoretical values for gas flow rates in the range between 300 and 1800 mL min(-1). The coupled denuder system (1,3,5-TMB-coated denuder as front-denuder coupled upstream of an alpha-CD/(129)I(-)-coated denuder) was applied successfully to separate test gas mixtures of ICl and I(2) at various mixing ratios in the laboratory. The operation of both denuder systems was demonstrated to be independent of relative humidity (0-100%) and storage period (at least 2 weeks prior to and after sampling). Detection limits were achieved at sub-parts-per-trillion-by-volume (sub-pptv) level. The presented method provides a reliable and practical approach for the speciation of gaseous iodine compounds. In addition, we report for the first time ambient air measurements of AIC mixing ratios, carried out at the atmospheric research station in Mace Head, Ireland. A maximum concentration of AIC of 30.2 pptv was observed for nighttime measurements and 6.0 pptv for daytime measurements. A similar diurnal pattern was found for I(2) with an average concentration level of 23.2 pptv during daytime and 85.1 pptv during nighttime, indicating a strong correlation with AIC.

Determination of Ultralow Level 129I/127I in Natural Samples by Separation of Microgram Carrier Free Iodine and Accelerator Mass Spectrometry Detection

DEFF Research Database (Denmark)

Hou, Xiaolin; Zhou, Weijian; Chen, Ning

2010-01-01

of 129I/127I, and a detection limit of this method for 129I is calculated to be 105 atoms. This will allow us to accurately determine 129I in prenuclear geological samples of low iodine concentration with 129I/127I of 10−12, such as loess, soil, coral, rock, sediment, and groundwater. Some samples......Separation of carrier free iodine from low iodine level samples and accurate measurement of ultralow level 129I in micrograms of iodine target are essential but a bottleneck in geological dating of terrestrial system and tracer research using naturally produced 129I. In this work, we present...... a carrier free method using coprecipitation of AgI with AgCl for preparing micrograms of iodine target, associated with combustion using a tube furnace for separating iodine from solid samples and anion exchange chromatography for preconcentrating iodine from a large volume of water. An accelerator mass...

Studies on 129I in bovine thyroid glands and investigations on revolatilization of iodine

International Nuclear Information System (INIS)

Glubrecht, H.; Kiselnic, L.; Handl, J.; Kuehn, W.

1979-01-01

In order to study fall out effect, deposition and revolatilization of iodine in the field and 129 I activity in bovine thyroid glands were studied. Deposition velocity of I 2 was 0.15 to 7 cm/sec, which was 100 times higher than that of CH 3 I. Biological half-life of iodine was 7.5 +- 0.5 d. In the contaminated plants, indifferent to the environmental conditions. However, the decrease of iodine concentration was not observed when the plants were cut off immediately after deposition of iodine. A sample of soil with or without plants was contaminated with iodine and re-emitted iodine was trapped by a charcoal filter. Iodine concentration was determined by I-specific electrodes after 1, 2, 4, and 8 hrs. In any case, I 2 was re-emitted immediately after the contamination. Bovine thyroid glands were dried by deep freezing and ground after the addition of KOH. Organic compounds were decomposed by stepwise heating up to 600 0 C. Then iodine was extracted by concentrated H 2 SO 4 and heated at 110 0 C. Evaporating iodine was adsorbed by a pure charcoal filter. By neutron activation analysis of the filter the activity of 129 I was 1.2 pCi/g iodine, which would be about 5 times higher than that measured in animals living far from nuclear installations. The distribution of stable iodine in thyroid gland was inhomogeneous. (Nakanishi, T.)

Investigations on iodine-129 in the biosphere

International Nuclear Information System (INIS)

Handl, J.; Oliver, E.; Jakob, D.

1992-01-01

In order to detect characteristic regional differences or temporal changes of iodine-129 concentrations in the biosphere, thyroids from humans, grazing livestock and roedeer (Capreolus capreolus L.) are collected in various parts of the world, which are differing in the exposure to I-129 immissions from nuclear sources. For reasons of comparison all samples are analysed for their I-129/I-127 atom ratios. Human thyroids taken from Lower Saxony (Federal Republic of Germany), which is a region not directly affected by reprocessing plants showed I-129/I-127 values between 8x10 -9 and 6x10 -8 for a period from February 1988 to September 1990. Those atom ratios correspond to the level of biospheric I-129 in background areas of Europe exposed to fallout atmospheric nuclear weapons tests during the 1950s and 1960s. Thyroid glands of roedeer taken from the Heby commune in Middle Sweden during spring 1990 showed I-129/I-127 ratios between 2x10 -7 and 4x10 -7 . Two soil samples taken from Krasnaya Gora and Mirny locations in Russia (about 200 km northwest of Chernobyl) exhibited ratios of about 1x10 -6 . According to the Cs-137 levels, the Swedish Heby area as well as both Russian locations were found to be seriously Chernobyl contaminated. Ratios found in human and bovine thyroids collected in the 10th Region in southern Chile (40deg-42degS) indicated values between 1x10 -10 and 9x10 -9 . On the basis of the prenuclear range of I-129/I-127 ratios between 4x10 -11 and 3x10 -9 , which were found in human thyroids analysed in the USA before 1945 the Chilean values can be considered only slightly elevated as compared to those determined in samples of Northern Hemisphere today. (orig.) [de

A review on speciation of iodine-129 in the environmental and biological samples

DEFF Research Database (Denmark)

Hou, Xiaolin; Hansen, Violeta; Aldahan, Ala

2009-01-01

As a long-lived beta-emitting radioisotope of iodine, I-129 is produced both naturally and as a result of human nuclear activities. At present time, the main part of I-129 in the environment originates from the human nuclear activity, especially the releases from the spent nuclear fuel reprocessi...

Determination of iodine 129 in environmental samples from Austria by neutron activation analysis

International Nuclear Information System (INIS)

Karg, V.; Schoenfeld, T.

1986-11-01

For various types of samples (thyroids from humans, from game and cows; ground water, snow and air filters) the 129 I-contents, expressed as 129 I/ 127 I-ratio (R), were determined by neutron activation analysis. The method utilises the neutron induced reactions 129 I(n, γ) 130 I and 127 I(n, 2n) 126 I. Four main steps are involved: 1. Separation of iodine from the sample and conversion to a form suitable for neutron irradiation. 2. Irradiation in a reactor. 3. Chemical processing of the irradiated material, i.e. separation of radio-iodine with addition of carrier. 4. Measurement of activities of 130 I and 126 I with a gammaspectrometer. The 129 I/ 127 I-ratio (R) is then obtained by comparing with the activities produced in a reference sample (usually with R = 1.0 x 10 -8 ) which is irradiated simultaneously. Details of the method are presented in the report. R-values between 0.6 x 10 -8 and 39 x 10 -8 were found. The highest values were those of snow and game thyroids. Ground water contained very little 129 I. The results confirm the expectation that 129 I enters the biosphere mainly via air and precipitation. (Author)

The chemical behaviour of iodine-129 in the process of radwaste conditioning

International Nuclear Information System (INIS)

Schon, T.

1993-11-01

During radwaste reprocessing, elemental I-129 may almost completely be transferred to the dissolver off-gas stream. The AC 6120 adsorbent, consisting of high-heated, amorphous silicic acid impregnated with silver nitrate, proved to be particularly efficient for removing the iodine from the off-gas. In a gas-solid reaction, the elemental iodine is converted into solid silver iodide and silver iodate. The reaction's stoichiometry depends on the loading temperature, with temperatures between 30 and 80 C resulting in a ratio of five between the reaction products of AgI and AgIO 3 , while with temperatures higher than that, up to 150 C, the ratio is three. For assessing the acceptability of the iodine-bearing AC 6120 as a waste product to be emplaced in a salt rock repository, the ratio of the reaction products is one of the main criteria. The products solubility and its complexation reactions with chloride-bearing brines are two other important criteria, especially with a view to the not completely hypothetical accident type of 'water ingress into the salt cavern'. Leaching experiments have shown that in this event, between 30 and over 60% of the waste product's iodine inventory would be leached out within only seven days. Thus AC 6120 is not a candidate adsorbent for immobilization of iodine 129 in a waste product. (orig./HP) [de

Iodine-129 in thyroids and tellurium isotopes in meteorites by neutron activation analysis

International Nuclear Information System (INIS)

Ballad, R.V.

1978-06-01

A combination of neutron activation and mass spectrometry has been used to determine the concentration of fissiogenic 129 I and the value of the 129 I/ 127 I ratio in thyroids of man, cow, and deer from Missouri. Deer thyroids show an average value of 129 I/ 127 I = 1.8 x 10 -8 and an average concentration of 3 x 10 -3 pCi 129 I per gram of thyroid (wet weight). Thyroids of cows and humans show successively lower values for the 129 I/ 127 I ratio and the 129 I content because their diets dilute fission-produced 129 I in the natural iodine cycle with mineral iodine. The results of analyses on a few thyroids from other geographic areas are also reported. The isotopic compositions of tellurium, krypton, and xenon were determined in acid-resistant residues of the Allende meteorite. Neutron activation and γ-counting were used to determine the relative abundances of six tellurium isotopes, and mass spectrometry was used to determine the isotopic compositions of krypton and xenon in aliquots of the same residues. Nucleogenetic anomalies were observed in the isotopic compositions of these three elements. The presence of isotopically distinct components of tellurium, krypton, and xenon in these residues provides strong support for the suggestion that our solar system formed directly from the debris of a supernova

Release of iodine from organic matter in natural water by K2S2O8 oxidation for 129I determination

DEFF Research Database (Denmark)

Dang, Haijun; Hou, Xiaolin; Roos, Per

2013-01-01

Accelerator mass spectrometry is the only method for measuring 129I in low level environmental samples. In this method, it is essential to convert organic associated iodine into inorganic form for the determination of total 129I or organic 129I because AgI is usually adopted as a target for AMS...... measurement of 129I. The chemical oxidative method to release iodine from organic matter in natural water was investigated using anion exchange chromatography and CHCl3 extraction methods. K2S2O8 was confirmed to be an ideal oxidative reagent for decomposing organic matters and converting organic iodine...... to inorganic form. More than 95% of iodine in natural water can be separated by solvent extraction after oxidation under optimal conditions, and the isotopic exchange of iodine in inorganic and organic forms was well completed during the oxidation, being able to result in an identical 129I/127I ratio...

Improved iodine and tritium control in reprocessing plants

International Nuclear Information System (INIS)

Henrich, E.; Schmieder, H.; Roesch, W.; Weirich, F.

1981-01-01

During spent fuel processing, iodine and tritium are distributed in many aqueous, organic and gaseous process streams, which complicates their control. Small modifications of conventional purex flow sheets, compatible with processing in the headend and the first extraction cycle are necessary to confine the iodine and the tritium to smaller plant areas. The plant area connected to the dissolver off-gas (DOG) system is suited to confine the iodine and the plant area connected to the first aqueous cycle is suited to confine the tritium. A more clear and convenient iodine and tritium control will be achieved. Relevant process steps have been studied on a lab or a pilot plant scale using I-123 and H-3 tracer

Dynamic model of the global iodine cycle for the estimation of dose to the world population from releases of iodine-129 to the environment

International Nuclear Information System (INIS)

Kocher, D.C.

1979-11-01

A dynamic linear compartment model of the global iodine cycle has been developed for the purpose of estimating long-term doses and dose commitments to the world population from releases of 129 I to the environment. The environmental compartments assumed in the model comprise the atmosphere, hydrosphere, lithosphere, and terrestrial biosphere. The global transport of iodine is described by means of time-invariant fractional transfer rates between the environmental compartments. The fractional transfer rates for 129 I are determined primarily from available data on compartment inventories and fluxes for naturally occurring stable iodine and from data on the global hydrologic cycle. The dose to the world population is estimated from the calculated compartment inventories of 129 I, the known compartment inventories of stable iodine, a pathway analysis of the intake of iodine by a reference individual, dose conversion factors for inhalation and ingestion, and an estimate of the world population. For an assumed constant population of 12.21 billion beyond the year 2075, the estimated population dose commitment is 2 x 10 5 man-rem/Ci. The sensitivity of the calculated doses to variations in some of the parameters in the model for the global iodine cycle is investigated. A computer code written to calculate global compartment inventories and dose rates and population doses is described and documented

Optimal buffer gas pressure for laser-induced fluorescence detection of the iodine-129 isotope in the atmosphere

International Nuclear Information System (INIS)

Kireev, S.V.; Pit'ko, A.V.; Shnyrev, S.L.

1995-01-01

The effect of atmospheric air pressure on the intensity of iodine-129 vapor fluorescence excited by a He-Ne (633 nm) laser is studied. It is shown that to achieve the maximum intensity of fluorescence of molecular iodine-129, it is advantageous, first, to use a 3 He- 20 Ne laser for excitation, and second, to detect atmospheric iodine impurities in the gas mixture under analysis evacuated to 2 x 10 18 - 4 x 10 18 mol/cm 3 . In this case, the sensitivity increases about twofold. 7 refs., 4 figs

Preparation of an apatite-based matrix for the confinement of iodine 129

International Nuclear Information System (INIS)

Audubert, F.

1995-01-01

The aim of this thesis is the study of the conditioning of iodine 129 from the reprocessing of nuclear wastes. Because of its long half life (1.57 10 7 years), the conditioning of iodine 129 requires a matrix stable during several thousands of years. The study of natural minerals allows the selection of mineral phases having a good long term behaviour. In the first part the policy of nuclear wastes management, and in particular of iodine, is recalled. A naturalistic approach is used to define the best conditioning material and the remarkable properties of apatite in this way are described. In the second part, the preparation and physical-chemical characterization of iodo-apatites are described. A demonstration is made that iodine can penetrate inside vanadate or lead phospho-vanadate apatite-based compounds. The third part deals with the preparation of the conditioning material. The sintering reaction under pressure allows the preparation of composite ceramics including iodo-apatite. A multi-layer coating process is defined: coating of PbI 2 with a Pb 3 (VO 4 ) 1.6 (PO 4 ) 0.4 layer and a Ca 10 (PO 4 ) 6 F 2 layer. Sintering is performed at 700 deg. celsius under a 25 MPa pressure. (J.S.)

Selection of chemical forms of iodine for transmutation of 129I

International Nuclear Information System (INIS)

Shirasu, Yoshiro; Minato, Kazuo

2003-01-01

To select suitable chemical forms of iodine for the target for transmutation of 129 I, the properties of iodine compounds of NaI, MgI 2 , CaI 2 , CuI and Ca(IO 3 ) 2 were compared and the out-of-reactor heating experiments of the pellets of CuI and Ca(IO 3 ) 2 with the cladding materials were carried out. CuI and Ca(IO 3 ) 2 are not deliquescent but stable in the air, which is of great advantage to construction, operation and maintenance of the processing plants. The cladding with Cu metal liner could be compatible with CuI though the compatibility of the stainless steel with CuI is not good. Ca(IO 3 ) 2 should be deleted from the list of the candidate target materials for the transmutation of 129 I due to the severe chemical reaction with the cladding materials

Combination of ozone feed and wet electrostatic precipitator. Experimental study of an innovative system to filter gaseous iodine and iodine containing particles

International Nuclear Information System (INIS)

Gouëllo, Mélany; Hokkinen, Jouni; Kärkelä, Teemu; Auvinen, Ari

2017-01-01

Efficient mitigation systems capable of reducing as much as possible the radioactive discharge to the environment in a severe Nuclear Power Plant (NPP) accident are a necessity. Nuclear Power Plants are equipped with filtration systems which have been characterized for aerosol retention in a short term, but to a far lesser extent for the retention of volatile iodine or for the long-term behaviour of the system. After the Fukushima accident, one of the main concerns of the nuclear industry has been to verify the ability of filtration systems to mitigate the possible source term to the environment. Radiotoxic iodine has a significant contribution to a possible source term in a severe NPP accident. An innovative system has been developed at VTT Technical Research Centre of Finland Ltd. to filter gaseous iodine and iodine containing particles (e.g. I x O y ). The system consists of a combination of an ozone feed and a modern wet electrostatic precipitator (WESP). The electrostatic precipitation (ESP) technique is widely used in the industry to filter out impurities (i.e. particles) in gases. The advantage of a WESP is that the impurities are removed from the system with a solution. They can thus directly be transported to a water container, such as the sump in a nuclear power plant. The addition of ozone feed at the inlet of the WESP allows the oxidation of gaseous iodine into particles. The efficiency of the system for the filtration of gaseous molecular iodine and methyl iodine has been tested and the subsequent observations are further discussed in this paper. The results showed that the combination of WESP together with ozone feed results in a good filtering efficiency against molecular iodine under air atmosphere and air/steam atmosphere. (author)

Some basic advantages of accelerator-driven transmutation of minor actinides and iodine-129

Energy Technology Data Exchange (ETDEWEB)

Shmelev, A.N.; Apse, V.A.; Kulikov, G.G. [Moscow Engineering Physics Institute (Russian Federation)

1995-10-01

The blanket of accelerator-driven facility designed for I-129 transmutation doesn`t contain fissile and fertile materials. So the overheating of iodine compounds transmuted is practically excluded. The efficacy of I-129 transmutation is estimated. Curium being accumulated in nuclear reactors can be incinerated in blanket of accelerator-driven facility. The deep depletion of curium diluted with inert material can be achieved.

Derivation of radioecological parameters from the long-term emission of iodine-129. Final report; Ableitung von radiooekologischen Parametern aus dem langfristigen Eintrag von Iod-129. Abschlussbericht

Energy Technology Data Exchange (ETDEWEB)

Michel, R.; Klipsch, K.; Ernst, T.; Gorny, M.; Jakob, D.; Vahlbruch, J. [Zentrum fuer Strahlenschutz und Radiooekologie (ZSR), Universitaet Hannover (Germany); Synal, H.A. [Paul Scherrer Inst., ETH Hoenggerberg, Zuerich (Switzerland); Schnabel, C. [Institut fuer Teilchenphysik, ETH Hoenggerberg, Zuerich (Switzerland)

2004-07-01

In this project, the distribution and behaviour of {sup 129}I and {sup 127}I in the environment and its pathways through the environment to man were comprehensively investigated in order to provide a basis for estimating the radiation exposure to man due to releases of {sup 129}I. To this end, the actual situation in Lower Saxony, Germany, was studied for exemplary regions near to and far from the coast of the North Sea. Accelerator mass spectrometry, radiochemical neutron activation analysis, ion chromatography, and ICP-MS were applied to measure the iodine isotopes, {sup 129}I and P{sup 127}I, in sea-water, air, precipitation, surface and ground waters, soils, plants, animals, foodstuffs, total diet, and human and animal thyroid glands. For air-borne iodine, the speciation as well as the particle size distribution of aerosols was determined. Soil depth profiles were investigated down to depths of 2.5 m in order to study the iodine migration as well as individual surface soil samples to allow for the determination of transfer factors of the iodine isotopes into plants. From the analytical results radioecological parameters for the long-term behaviour of {sup 129}I in the pedo- and biosphere were derived. The iodine isotopes are in severe disequilibrium in the different environmental compartments. The pre-nuclear equilibrium {sup 129}I/{sup 127}I ratio in the biosphere was determined to be 2.0 x 10{sup -13} with a geometric standard deviation of 1.39. Today, the environmental isotopic ratios in Northern Germany range from 10{sup -6} to 10{sup -10}. The highest ratios are found in North Sea water, the lowest in deep soil samples and ground water. The North Sea appears as the dominant source of air-borne iodine in Northern Germany due to the emissions of European reprocessing plants. The results are discussed with respect to their radiological relevance and in view of the general protection of the environment, i.e. air, water, soil and the biosphere. (orig.)

Environmental behavior of technetium-99 and iodine-129

International Nuclear Information System (INIS)

Garland, T.R.; Schreckhise, R.G.

1982-01-01

The environmental behavior of technetium-99 and iodine-129 was once thought to be similar, particularly with respect to their soil solubility and biological interactions. Over the past several years, the comparative behavior of these two anions has been studied with respect to their fate in natural environments (both aquatic and terrestrial). The mechanisms studied include physical, chemical and biological parameters that account for differences in soil behavior, cycling between soil and/or air to vegetation, adsorption and metabolism in plants, and their availability and fate following ingestion by animals

The iodine reactivity; La reactivite de l'iode

Energy Technology Data Exchange (ETDEWEB)

NONE

2003-07-01

The iodine is an important element because it has long life isotopes (such as iodine 129) and a great mobility in natural media. Iodine presents a complex chemistry because of its volatility and its strong redox reactivity. The S.E.C.R. works to better understand the reactivity of this element in different natural, industrial or biological environments. It plays a part in thermochemical sites as a possible way of hydrogen formation. This seminar gives some aspects relative to the chemical reactivity of iodine, since its thermochemistry in the I/S cycles to produce hydrogen to its reactivity in the natural medium and its potential radiological impact. This document includes 4 presentations transparencies dealing with: the {sup 129}I cycle rejected in the low radioactive gaseous and liquid effluents of the La Hague reprocessing plant (C. Frechou); a bibliographic review of iodine retention in soils (F. Bazer-Bachi); the hydrogen production and the iodine/sulfur thermochemical cycle (role of iodine in the process); and the direct characterization by electro-spray ionization mass spectroscopy of iodine fixation by fulvic acids (P. Reiller, B. Amekraz, C. Moulin, V. Moulin)

Standardization of iodine-129 by the TDCR liquid scintillation method and 4π β-γ coincidence counting

Science.gov (United States)

Cassette, P.; Bouchard, J.; Chauvenet, B.

1994-01-01

Iodine-129 is a long-lived fission product, with physical and chemical properties that make it a good candidate for evaluating the environmental impact of the nuclear energy fuel cycle. To avoid solid source preparation problems, liquid scintillation has been used to standardize this nuclide for a EUROMET intercomparison. Two methods were used to measure the iodine-129 activity: triple-to-double-coincidence ratio liquid scintillation counting and 4π β-γ coincidence counting; the results are in good agreement.

An improved analytical method for iodine-129 determination in low-level radioactive waste

Energy Technology Data Exchange (ETDEWEB)

Hsieh, Yi-Kong; Wang, TsingHai; Jian, Li-Wei; Chen, Wei-Han; Wang, Chu-Fang [National Tsing Hua Univ., Hsinchu, Taiwan (China). Dept. of Biomedical Engineering and Environmental Sciences; Tsai, Tsuey-Lin [Atomic Energy Council, Taiwan (China). Chemical Analysis Div.

2014-07-01

In this study, an alkaline-digestion pretreatment and a subsequent ICP-MS measurement were conducted for iodine-129 (I-129) determination in low-level radioactive waste. A TMAH + H{sub 2}O{sub 2} + Triton X-100 mixed alkaline digestion was the most effective mixture for I-129 determination. Using this alkaline reagent, a high level of I-129 recovery (101 ± 6%) was achieved for the analysis of the I-129-spiked standard reference materials NIST 2709 and 2711. Importantly, the I-129 concentrations determined for ten real samples provided by the Lan-Yu radioactive waste temporary storage site were found to be below the detection limit (0.011 mg/kg). This value was only approximately 30-70% of the values determined using the I-129/Cs-137 scaling factor. This means that using the I-129/Cs-137 scaling factor severely overestimates the I-129 concentration in these low-level radioactive wastes. We therefore suggest that a detailed re-inspection of the I-129/Cs-137 scaling factor should be performed to appropriately categorize these low-level radioactive wastes.

Detection of iodine-129 in some environmental samples

International Nuclear Information System (INIS)

Ikeda, Nagao

1981-01-01

The recent accumulation of the long-lived isotope of iodine, 129 I, which is released in environment by the peaceful use of nuclear energy or nuclear test explosion is becoming important in the view point of the internal exposure by the low level radiation. The studies on the detection of determination of 129 I in environmental samples so far published are still very few. The authors tried to detect 129 I in some Japanese seaweeds and soil samples with the aid of the activation method by using the nuclear reaction of 129 I(n, #betta#) 130 I. The samples analysed in this work are tangle (Laminaria japonica) for daily food grown in Hidaka, Hokkaido and uncultivated soil collected in Tokai, Ibaraki Pref. As the #betta#-ray peak indicator for 130 I, cesium oxide and the aged radioisotope product of 131 I are also subjected to the neutron irradiation. From cesium oxide, 130 I is formed by the reaction of 133 Cs(n, α) 130 I. An aged vial of the 131 I product is expected to contain very minute amounts of 129 I which is also produced both by the fission of uranium and neutron capture reaction of tellurium followed by #betta# - -decay. The #betta#-ray spectra for the soil sample, cesium oxide and the aged 131 I vial are shown in Fig. 1. No appreciable peak was found for the seaweeds sample. In the #betta#-ray spectra for irradiated cesium oxide and the aged 131 I vial, several typical peaks for 130 I were observed. By comparing with these peaks, several small peaks which appear at around 418, 536 and 739 keV in the soil sample can be attributed to those of 130 I. The 129 I content in the soil sample is roughly estimated to be 2 x 10 - 10 Bq/g. (author)

Retention of gaseous isotopes

International Nuclear Information System (INIS)

Yarbro, O.O.; Mailen, J.C.; Stephenson, M.J.

1977-01-01

Retention of gaseous fission products during fuel reprocessing has, in the past, been limited to a modest retention of 131 I when processing fuels decayed less than about 180 days. The projected rapid growth of the nuclear power industry along with a desire to minimize environmental effects is leading to the reassessment of requirements for retention of gaseous fission products, including 131 I, 129 I, 85 Kr, 3 H, and 14 C. Starting in the late 1960s, a significant part of the LMFBR reprocessing development program has been devoted to understanding the behavior of gaseous fission products in plant process and effluent streams and the development of advanced systems for their removal. Systems for iodine control include methods for evolving up to 99% of the iodine from dissolver solutions to minimize its introduction and distribution throughout downstream equipment. An aqueous scrubbing system (Iodox) using 20 M HNO 3 as the scrubbing media effectively removes all significant iodine forms from off-gas streams while handling the kilogram quantities of iodine present in head-end and dissolver off-gas streams. Silver zeolite is very effective for removing iodine forms at low concentration from the larger-volume plant off-gas streams. Removal of iodine from plant liquid effluents by solid sorbents either prior to or following final vaporization appears feasible. Krypton is effectively released during dissolution and can be removed from the relatively small volume head-end and dissolver off-gas stream. Two methods appear applicable for removal and concentration of krypton: (1) selective absorption in fluorocarbons, and (2) cryogenic absorption in liquid nitrogen. The fluorocarbon absorption process appears to be rather tolerant of the normal contaminants (H 2 O, CO 2 , NOsub(x), and organics) present in typical reprocessing plant off-gas whereas the cryogenic system requires an extensive feed gas pretreatment system. Retention of tritium in a reprocessing plant is

An Anthropogenic Radioisotope, Iodine 129, As A Tracer For Studying The Northern Limb of The Meridional Overturning Circulation (moc)

Science.gov (United States)

Gascard, J. C.; Raisbeck, G.; Yiou, F.; Sequeira, S.; Mork, K. A.

A number of observations taken during the 1990s, seem to corroborate the fact that the northern limb of the Meridional Overturning Circulation (the so-called MOC), is undergoing large scale variability. Arctic Sea-Ice thinning, Overflows slackening, Labrador and Greenland Seas Deep Convection weakening, have recently been re- ported. Can this large scale variability be interpreted as a natural variability of the MOC or is it more related to global changes due to anthropogenic effects like green- house gases enhancing Global Warming at High Latitudes ? Iodine 129 resulting from reprocessing nuclear wastes at La Hague (France) and Sellafield (UK), has penetrated through all the various parts of the MOC from the Source: the Norwegian Coastal Current (NCC) collecting Iodine 129 from the North Sea, to the Sink: the Greenland- Iceland-Scotland Overflows and ultimately to the North Atlantic Deep Waters via the Deep Western Boundary Current. During recent years, discharges of Iodine 129 have increased drastically and peaks in Iodine 129 concentrations have already been ob- served all along the coast of Norway. In this talk, we will first present the most recent results showing the transfer of Iodine 129 through the various parts of the MOC from the NCC down to the North Atlantic Overflows (Denmark Strait), and second, explain how this results allow us to improve our understanding of the MOC system and in particular its variability. This is an important issue for improving reliability of actual numerical simulations of past, present and future behavior of the MOC, which has strong implications for climate related problems.

A review on speciation of iodine-129 in the environmental and biological samples

Energy Technology Data Exchange (ETDEWEB)

Hou Xiaolin [Riso National Laboratory for Sustainable Energy, NUK-202, Technical University of Denmark, DK-4000 Roskilde (Denmark)], E-mail: xiaolin.hou@risoe.dk; Hansen, Violeta [Riso National Laboratory for Sustainable Energy, NUK-202, Technical University of Denmark, DK-4000 Roskilde (Denmark); Aldahan, Ala [Department of Earth Science, Uppsala University, SE-758 36 Uppsala (Sweden); Possnert, Goeran [Tandem Laboratory, Uppsala University, SE-751 21 Uppsala (Sweden); Lind, Ole Christian [Norwegian University of Life Science, N-1432, As (Norway); Lujaniene, Galina [Institute of Physics, Savanoriu 231, LT-0230 Vilnius (Lithuania)

2009-01-26

As a long-lived beta-emitting radioisotope of iodine, {sup 129}I is produced both naturally and as a result of human nuclear activities. At present time, the main part of {sup 129}I in the environment originates from the human nuclear activity, especially the releases from the spent nuclear fuel reprocessing plants, the {sup 129}I/{sup 127}I ratios have being reached to values of 10{sup -10} to 10{sup -4} in the environment from 10{sup -12} in the pre-nuclear era. In this article, we review the occurrence, sources, inventory, and concentration level of {sup 129}I in environment and the method for speciation analysis of {sup 129}I in the environment. Measurement techniques for the determination of {sup 129}I are presented and compared. An overview of applications of {sup 129}I speciation in various scientific disciplines such as radiation protection, waste depository, and environmental sciences is given. In addition, the bioavailability and radiation toxicity (dose to thyroid) of {sup 129}I are discussed.

Iodine 129 measurements by gamma spectrometry in biological samples. Results in seaweeds (Fucus serratus et laminaria digitata)

International Nuclear Information System (INIS)

Maro, D.; Hebert, D.; Gandon, R.; Solier, L.

1999-01-01

A iodine selective radiochemistry method was developed to measure 129 I(period 1,57 x 10 10 7 years) by gamma spectrometry in biological samples. This method avoids using neutron activation analysis or accelerator mass spectrometry. The method is based on iodine extraction from samples in order to obtain an aqueous matrix with no attenuation agent except 127 I(stable isotope). The parallel determination of 127 I allows to correct 129 I measurements for self attenuation and also monitor seasonal changes in iodine metabolism in biological species. Measurements were performed in two seaweed species (Fucus serratus and Laminaria digitata) samples in the area of La Hague reprocessing plant discharge between January and February 1997). Samples from stations close to the point of release (Goury and Herquemoulin), showed 129 I activities around 60 Bq kg -1 dry weight in Fucus serratus and around 300 Bq kg -1 dry weight in Laminaria digitata. 300 km away from the realize point, 129 I activities were 10 Bq kg -1 dry weight in Fucus serratus and 171 Bq kg -1 dry weight in Laminaria digitata. 127 I concentrations were between 547 and 1,232 mg kg -1 dry weight in Fucus serratus and between 6,624 and 14,296 mg kg -1 dry weight in Laminaria digitata. (authors)

Determination of ultra-low level ¹²⁹I in vegetation using pyrolysis for iodine separation and accelerator mass spectrometry measurements

DEFF Research Database (Denmark)

Hou, Xiaolin; Wang, Yanyun

2016-01-01

Radioactive isotopes of iodine are the most common radiological toxins from nuclear accidents due to their high release and high enrichment in human thyroid. Among the radioactive isotopes, long-lived 129I can not only be used for the estimation of the radioactive risk of short-lived radioactive...... and ultra-low concentration in normal environmental and biological samples, it is important to efficiently separate iodine from the sample matrix and sensitively measure 129I. However, the complicated chemical properties of iodine and high organic content in biological samples make efficient separation...... of iodine very difficult using conventional acid digestion and alkaline ashing methods. By optimizing the key parameters related to the separation of iodine by pyrolysis using a tube furnace, including carbonization temperature, heating protocol, combustion assisting gas, iodine volatilization process...

Iodine-129, Iodine-127 and Caesium-137 in the environment: soils from Germany and Chile

International Nuclear Information System (INIS)

Daraoui, A.; Michel, R.; Gorny, M.; Jakob, D.; Sachse, R.; Synal, H.-A.; Alfimov, V.

2012-01-01

Soil profiles from Bavaria in southern Germany and from Chile were analysed for 129 I by accelerator mass spectrometry (AMS), for 127 I by inductively coupled plasma mass spectrometry (ICP-MS), and for 137 Cs by gamma-spectrometry. The mean deposition density of 137 Cs in soils from Bavaria was (41 × 1.5 ±1 ) kBq m −2 (geometric mean and geometric standard deviation), originating mostly from the Chernobyl fall-out. The deposition density of 129 I in these soils was (109 × 1.5 ±1 ) mBq m −2 . The dominant sources of 129 I in Bavaria are, however, the reprocessing plants La Hague and Sellafield and not the Chernobyl fall-out. The 129 I/ 127 I isotopic ratios of the Bavarian soils were between 10 −7 and 10 −10 , i.e. 10 2 –10 5 times higher than the ratios observed for the samples from Chile. The 129 I integral deposition densities in Chile, Easter Island and Antarctica were between 0.3 mBq m −2 and 2 mBq m −2 . In these soils, the observed 129 I/ 127 I ratios were about 10 −12 . The soils from Chile allow the determination of the 129 I fall-out from the atmospheric nuclear weapons explosions undisturbed from contaminations due to releases from reprocessing plants. An upper limit of the integral 129 I deposition density of the atmospheric nuclear weapons explosions on the Southern Hemisphere (27°S) is about 1 mBq m −2 . Finally, the dependence of the migration behaviour of 137 Cs, 127 I and of 129 I on the soil properties is discussed. It turns out that there is a distinctly different behaviour of 127 I, 129 I, and 137 Cs in the soils exhibiting different sorption mechanisms for old and recent iodine as well as for 137 Cs. - Highlights: ► I-129 from European reprocessing plants drastically changed its natural abundances. ► We report here inventories of the Cs-137 and I-129 in Bavaria and Chile. ► The dominant sources of I-129 in Bavaria are the European reprocessing plants. ► The dominant sources of I-129 in Chile are the atmospheric

129I Moessbauer spectroscopic study of several n-σ charge-transfer complexes of iodine with thioethers

International Nuclear Information System (INIS)

Sakai, Hiroshi; Matsuyama, Tomochika; Maeda, Yutaka

1986-01-01

129 I Moessbauer studies have been made of n-σ charge-transfer complexes of iodine with thioethers, such as thiane, 1,4-oxathiane, and 1,4-dithiane. The spectra of these complexes consist of two sets of quadrupole octets, corresponding to the bridging and terminal iodine atoms. The transferred charges from the thioethers are localized on the terminal iodine atoms, and the bridging iodine atoms have slightly positive charges. This result can be well explained in terms of a covalent bond between the sulfur and bridging iodine atoms or the MO treatment of a delocalized three-center four-electron bonding. The contributions of the dative structure to the ground state are estimated to be 36, 28, and 24 % for thiane-iodine, 1,4-oxathiane-iodine, and 1,4-dithiane-iodine respectively. The nature of the charge-transfer bond is discussed in comparison with amine-iodine complexes. (author)

LWR severe accident simulation: Iodine behaviour in FPT2 experiment and advances on containment iodine chemistry

Energy Technology Data Exchange (ETDEWEB)

Girault, N., E-mail: nathalie.girault@irsn.fr [Institut de Radioprotection et de Surete Nucleaire (IRSN), BP3 - 13115 St.-Paul-lez-Durance (France); Bosland, L. [Institut de Radioprotection et de Surete Nucleaire (IRSN), BP3 - 13115 St.-Paul-lez-Durance (France); Dickinson, S. [National Nuclear Laboratory, Harwell, Oxon OX11 0QT (United Kingdom); Funke, F. [AREVA NP Gmbh, PO Box 1109, 91001 Erlangen (Germany); Guentay, S. [Paul Scherrer Institut, 5232 Villigen PSI (Switzerland); Herranz, L.E. [Centro des Investigaciones Energeticas, MedioAmbiantales y Tecnologicas, av. Complutense 2, 28040 Madrid (Spain); Powers, D. [Sandia National Laboratories, New Mexico, PO Box 5800, Albuquerque, NM 87185 (United States)

2012-02-15

the iodine behaviour in the FPT2 containment vessel based on dedicated small-scale analytical experiments and computer codes calculations. Other investigations dealing with primary circuit and sump chemistry are also reported. These could help to scale the results of Phebus-FP tests to reactor accidents. Modelling studies were generally successful when a gaseous iodine injection from the primary circuit was assumed. Indeed, though each of the iodine codes has specific iodine chemistry features that should be further developed and each approach to the modelling is distinct, the overall iodine behaviour in the FPT2 containment is generally well reproduced by the models that predict: Bullet a low final gaseous iodine concentration in the containment atmosphere, Bullet a predominant iodine concentration in the sump and to a lesser extent a significant iodine deposition on containment surfaces. The main code-to-code differences, in the results obtained in gaseous iodine speciation, come from the various treatments of gaseous radiolytic reactions. Calculations that include the radiolytic conversion of volatile iodine into iodine oxide particulate show there is a persistence of both gaseous iodine and iodine oxide particles in the atmosphere. There are also some variations between the predicted organic iodine concentrations that depend mainly on the initial assumptions. A key aspect of the Phebus FPT2 test interpretation is that the long term iodine behaviour in the containment can be explained by exchanges between organic iodide released from painted surfaces and inorganic iodine released from deposited aerosol on the containment walls. Further studies of regulatory significance on sump chemistry showed that the gaseous iodine control that was evident in the Phebus tests through silver release and/or alkaline buffered sump solutions may not be assured. As most of the past iodine aqueous chemistry studies were done with rather pure systems and because of the uncompleted

Iodine-129: a study of its transport in the environment and distribution in biological systems. Progress report, June 1, 1975--May 31, 1976

International Nuclear Information System (INIS)

Manuel, O.K.

1976-02-01

During this second year of our study on the transport and distribution of 129 I, most of our efforts have been given to analyses of iodine in representative samples of milk, surface water, precipitation, plants, and mineral iodine. The results of our earlier analyses on 129 I and 127 I in thyroids of grazing animals have been reported in a manuscript which is to appear in Health Physics. The results of recent analyses on 129 I in two iodine-rich minerals, iodyrite (AgI) and marshite (CuI), establish limits on the initial isotopic composition of iodine, 1.5 x 10 -14 less than or equal to 129 I/ 127 I less than or equal to 1.0 x 10 -13 , present when the minerals formed. These results have been reported in a manuscript submitted to the Journal of Inorganic and Nuclear Chemistry. Our 100 additional analyses have been made on 129 I and 127 I in various types of mammalian thyroid glands from this area, in milk, precipitation, and surface water, and in interlaboratory monitors. A program has been established for systematic sampling of 129 I in milk, surface waters, and precipitation. This program will permit us to look for evidence of the spring fallout peak and thus provide information on the stratospheric contribution of 129 I to this area

IODES, Calculating the Estimation of Dose to the World Population from Releases of Iodine-129 to the Environment

International Nuclear Information System (INIS)

2002-01-01

1 - Description of program or function: IODES is a dynamic linear compartment model of the global iodine cycle which estimates long-term doses and dose commitments to the world population from releases of 129 I to the environment. The global environment is divided into different compartments comprising the atmosphere, hydrosphere, lithosphere, and terrestrial biosphere. The global transport of iodine is described by means of time-invariant fractional transfer rates between the environmental compartments. The fractional transfer rates for 129 I are determined primarily from available data on compartment inventories and fluxes for naturally occurring stable iodine and from data on the global hydrologic cycle. The dose to the world population is estimated from the calculated compartment inventories of 129 I, the known compartment inventories of stable iodine, a pathway analysis of the intake of iodine by a reference individual, dose conversion factors for inhalation and ingestion, and an estimate of the world population. For an assumed constant population of 12.21 billion beyond the year 2075, the estimated population dose commitment is 2 x 105 man-rem/Ci. 2 - Methods: IODES calculates 129 I inventories in the different environmental compartments and individual and population doses as a function of time after a release to the environment by solving a set of simultaneous first-order linear differential equations using numerical methods. 3 - Restrictions on the complexity of the problem: - The subroutine LSODE for solving the differential equations is provided online at the ORNL computer center and, thus, is not included in the IODES code package. If the LSODE routine is not available to the user, then an appropriate differential equation routine must be supplied by the user, and the initialization of parameters and the call statement for LSODE in the main program must be changed accordingly

Radioecological studies on plutonium and iodine-129 in the surroundings of the Karlsruhe reprocessing plant

International Nuclear Information System (INIS)

Schuettelkopf, H.; Pimpl, M.

1982-01-01

Plutonium and 129 I are emitted from the Karlsruhe Reprocessing Plant (WAK) together with exhaust air and liquid effluents. Plutonium dispersion in the environment was used to calculate the dispersion factors, to determine the rates of deposition on grass and of the total deposition rates, to measure the distribution at depth of plutonium in the soil and to evaluate the contamination of plants and animals in the environment of the Karlsruhe Reprocessing Plant. The plutonium emissions with the liquid effluents were studied to deepen understanding of the process of sedimentation in a river system. Sediments, water samples, aerosols and living organisms from the Altrhein were examined. Factors of transfer to various organisms living in the Altrhein were measured. Most of the 129 I release from WAK goes via the exhaust air: this even applies after installation of an iodine filter into the exhaust air stack. The 129 I contamination of the environmental air, the soil, thyroids and milk was measured. Regarding the milk/air concentration ratio, a mean value of 210 was determined with a scattering range of 50 to 1480. Soil contamination was studied very thoroughly. Iodine-129 is transported into lower soil layers at a very slow rate only, if at all. The contamination of the soil with 129 I remained largely constant during the three years of investigations. The low rates of deposition of 0.02 to 0.05 cm/s indicate that 129 I is released to the environmental air again from plants undergoing the process of rotting. (author)

Experimental study on iodine chemistry (EXSI) - Containment experiments with elemental iodine

Energy Technology Data Exchange (ETDEWEB)

Kaerkelae, T.; Auvinen, A. (VTT Technical Research Centre of Finland (Finland)); Holm, J.; Ekberg, C. (Chalmers Univ. of Technology (Sweden)); Glaenneskog, H. (Vattenfall Power Consultant (Sweden))

2009-10-15

The behaviour of iodine during a severe accident has been studied in several experimental programs, ranging from the large-scale PHEBUS FP tests and intermediate-scale ThAI tests to numerous separate effect studies. Oxidation of iodine in gas phase has been one of the greatest remaining uncertainties in iodine behaviour during a severe accident. In this study the possible formation of iodine oxide aerosol due to radiolytic oxidation of gaseous iodine is experimentally tested and the reaction products are analysed. The experimental facility applied in this study is based on the sampling system built at VTT for ISTP program project CHIP conducted IRSN. The experimental facility and the measuring technology are sophisticated and unique in the area of nuclear research as well as in the field of aerosol science. The results from the experiments show an extensive particle formation when ozone and gaseous iodine react with each other. The formed particles were collected on filters, while gaseous iodine was trapped into bubbles. The particles were iodine oxides and the size of particles was approximately 100 nm. The transport of gaseous iodine through the facility decreased when both gaseous iodine and ozone were fed together into facility. Experimental study on radiolytic oxidation of iodine was conducted in co-operation between VTT and Chalmers University of Technology as a part of the NKS-R programs. (author)

Experimental study on iodine chemistry (EXSI) - Containment experiments with elemental iodine

International Nuclear Information System (INIS)

Kaerkelae, T.; Auvinen, A.; Holm, J.; Ekberg, C.; Glaenneskog, H.

2009-10-01

The behaviour of iodine during a severe accident has been studied in several experimental programs, ranging from the large-scale PHEBUS FP tests and intermediate-scale ThAI tests to numerous separate effect studies. Oxidation of iodine in gas phase has been one of the greatest remaining uncertainties in iodine behaviour during a severe accident. In this study the possible formation of iodine oxide aerosol due to radiolytic oxidation of gaseous iodine is experimentally tested and the reaction products are analysed. The experimental facility applied in this study is based on the sampling system built at VTT for ISTP program project CHIP conducted IRSN. The experimental facility and the measuring technology are sophisticated and unique in the area of nuclear research as well as in the field of aerosol science. The results from the experiments show an extensive particle formation when ozone and gaseous iodine react with each other. The formed particles were collected on filters, while gaseous iodine was trapped into bubbles. The particles were iodine oxides and the size of particles was approximately 100 nm. The transport of gaseous iodine through the facility decreased when both gaseous iodine and ozone were fed together into facility. Experimental study on radiolytic oxidation of iodine was conducted in co-operation between VTT and Chalmers University of Technology as a part of the NKS-R programs. (author)

Deposition velocity of gaseous organic iodine from the atmosphere to rice plants

International Nuclear Information System (INIS)

Muramatsu, Yasuyuki; Shigeo-Uchida; Sumiya, Misako; Ohmomo, Yoichiro

1996-01-01

To obtain parameter values for the assessment of 129 I transfer from the atmosphere to rice, deposition of CH 3 I to rice plants has been studied. The mass normalized deposition velocity (V D ) of CH 3 I for rough (unhulled) rice was 0.00048 cm 3 g -1 s -1 , which is about 1/300 of that of I 2 . Translocation of iodine, deposited as CH 3 I on leaves and stems, to rice grain was negligibly small. Distribution of iodine between hull and inner part of the grain was found to depend also on the chemical forms of atmospheric iodine to be deposited. The ratio of the iodine distribution in a grain exposed to CH 3 I was as follows: rough rice: brown rice (hulled rice):polished rice = 1.0:0.49:0.38. The distribution ratio in polished grains for CH 3 I exposed rice was about 20 times higher than that for I 2 . 22 refs., 1 fig., 6 tabs

New technique for determination of long-lived radioisotopes, Iodine-129, using multiparameter coincidence spectrometry

International Nuclear Information System (INIS)

Hatsukawa, Yuichi; Oshima, Masumi; Toh, Yosuke; Shinohara, Nobuo; Kushita, Kosuke; Ueno, Takashi

2003-01-01

Multiparameter coincidence γ-ray spectrometry based on g-g coincidence is widely used in the field of nuclear structure studies, and has produced many successful results. In this study, feasibility of the method for neutron activation analysis of long lived iodine isotope, 129 I, was investigated. (author)

Chemical and physical factors which control the substitution reactions of direct fission-produced iodine with gaseous methane and the methyl halides

International Nuclear Information System (INIS)

Kikuchi, M.; Church, L.B.

1976-01-01

The factors controlling the hydrogen and halogen substitution reactions resulting from direct fission-produced iodine isotopes (*I) with gaseous methane and methyl halides were investigated. The chemical reaction probabilities, corrected for any secondary decomposition, were compared as a function of various chemical and physical parameters. These include carbon-halogen bond strength, halogen electronegativity, volume and cross sectional area of the substituted and neighboring atoms. On the basis of this analysis, it is concluded that *I-for-X (where X = H, F, Cl, Br and I) substitution reactions are controlled by the cross sectional area of the X atom. The *I-for-H substitution probability is reduced in proportion to the volume of X, suggesting that steric interference is the dominant factor influencing the reaction probability. (orig.) [de

World-wide redistribution of 129Iodine from nuclear fuel reprocessing facilities: Results from meteoric, river, and seawater tracer studies

International Nuclear Information System (INIS)

Moran, J.E.; Oktay, S.; Santschi, P.H.; Schink, D.R.; Fehn, U.; Snyder, G.

1999-01-01

Releases of the long-lived radioisotope of iodine, 129 I, from commercial nuclear fuel reprocessing facilities in England and France have surpassed natural, and even bomb test inventories. 129 I/ 127 I ratios measured in a variety of environmental matrices from Europe, North America and the southern hemisphere show the influence of fuel reprocessing-derived 129 I, which is transported globally via the atmosphere. Transport and cycling of I and 129 I in the hydrosphere and in soils are described based on a spatial survey of 129 I in freshwater. (author)

Extensive Evaluation of a Diffusion Denuder Technique for the Quantification of Atmospheric Stable and Radioactive Molecular Iodine

DEFF Research Database (Denmark)

Huang, Ru-Jin; Hou, Xiaolin; Hoffmann, Thorsten

2010-01-01

In this paper we present the evaluation and optimization of a new approach for the quantification of gaseous molecular iodine (I2) for laboratory- and field-based studies and its novel application for the measurement of radioactive molecular iodine. α-Cyclodextrin (α-CD) in combination with 129I......, and condition of release and derivatization of iodine, is extensively evaluated and optimized. The collection efficiency is larger than 98% and the limit of detection (LOD) obtained is 0.17 parts-per-trillion-by-volume (pptv) for a sampling duration of 30 min at 500 mL min−1. Furthermore, the potential use...... of this protocol for the determination of radioactive I2 at ultra trace level is also demonstrated when 129I− used in the coating is replaced by 127I− and a multiple denuder system is used. Using the present method we observed 25.7−108.6 pptv 127I2 at Mweenish Bay, Ireland and 108 molecule m−3 129I2 at Mainz...

Observation of radioactive iodine ({sup 131}I, {sup 129}I) in cropland soil after the Fukushima nuclear accident

Energy Technology Data Exchange (ETDEWEB)

Fujiwara, Hideshi, E-mail: hfuji@affrc.go.jp

2016-10-01

During the early stages of the Fukushima nuclear accident, the temporal variations of {sup 131}I deposited on the ground and of {sup 131}I accumulated in cropland soil were monitored at a fixed location in Japan. Moreover, concentrations of long-lived radioactive iodine ({sup 129}I) in atmospheric deposits and soil were measured to examine the feasibility of retrospectively reconstructing {sup 131}I levels from the levels of accident-derived {sup 129}I. The exceptionally high levels of {sup 131}I in deposits and soil were attributed to rainfall-related deposition of radionuclides. In the crop field studied, the losses of deposited {sup 131}I and {sup 129}I due to volatilization were small. The atomic ratio {sup 129}I/{sup 131}I in the topsoil corresponded to the same ratio in deposits. The {sup 131}I concentrations measured in the topsoil were very consistent with the {sup 131}I concentrations reconstructed from the {sup 129}I concentrations in the soil. - Highlights: • A high level of {sup 131}I contamination occurs through rainfall-related deposition. • Only a small loss of deposited radioactive iodine occurs via volatilization. • The {sup 129}I/{sup 131}I ratio in soil corresponds to the ratio in atmospheric deposit. • The feasibility of retrospectively reconstructing {sup 131}I is confirmed.

Preparation of an apatite-based matrix for the confinement of iodine 129; Mise au point d`une matrice apatitique pour le confinement de l`iode 129

Energy Technology Data Exchange (ETDEWEB)

Audubert, F

1995-11-08

The aim of this thesis is the study of the conditioning of iodine 129 from the reprocessing of nuclear wastes. Because of its long half life (1.57 10{sup 7} years), the conditioning of iodine 129 requires a matrix stable during several thousands of years. The study of natural minerals allows the selection of mineral phases having a good long term behaviour. In the first part the policy of nuclear wastes management, and in particular of iodine, is recalled. A naturalistic approach is used to define the best conditioning material and the remarkable properties of apatite in this way are described. In the second part, the preparation and physical-chemical characterization of iodo-apatites are described. A demonstration is made that iodine can penetrate inside vanadate or lead phospho-vanadate apatite-based compounds. The third part deals with the preparation of the conditioning material. The sintering reaction under pressure allows the preparation of composite ceramics including iodo-apatite. A multi-layer coating process is defined: coating of PbI{sub 2} with a Pb{sub 3}(VO{sub 4}){sub 1.6}(PO{sub 4}){sub 0.4} layer and a Ca{sub 10}(PO{sub 4}){sub 6}F{sub 2} layer. Sintering is performed at 700 deg. celsius under a 25 MPa pressure. (J.S.). 131 refs.

Laboratory report on iodine (¹²⁹I and ¹²⁷I) speciation, transformation and mobility in Handford groundwater, suspended particles and sediments

Energy Technology Data Exchange (ETDEWEB)

Santschi, P. H. [Texas A & M Univ., College Station, TX (United States); Xu, C. [Texas A & M Univ., College Station, TX (United States); Zhang, S. [Savannah River Site (SRS), Aiken, SC (United States). Savannah River National Lab. (SRNL); Ho, Y. [Texas A & M Univ., College Station, TX (United States); Li, H. [Texas A & M Univ., College Station, TX (United States); Schwehr, K. [Texas A & M Univ., College Station, TX (United States); Kaplan, D. I. [Savannah River Site (SRS), Aiken, SC (United States). Savannah River National Lab. (SRNL)

2012-09-01

The Hanford Site in eastern Washington produced plutonium for several decades and in the process generated billions of gallons of radioactive waste. Included in this complex mixture of waste was 50 Ci of iodine-129 (¹²⁹I). Iodine-129’s high abundance, due to its high fission yield, and extreme toxicity result in iodine-129 becoming a key risk driver at many Department of Energy (DOE) sites. The mobility of radioiodine in arid environments, such as the Hanford Site, depends largely on its chemical speciation and is also greatly affected by many other environmental factors, especially natural sediment organic matter (SOM). Groundwater radioiodine speciation has not been measured in arid regions with major plumes or large disposed ¹²⁹I inventories, including the Hanford Site, Idaho National Laboratory, and Nevada Test Site. In this study, stable iodine-127 and radioiodine-129 speciation, pH, and dissolved organic carbon (DOC) of groundwater samples collected from seven wells located in the 200-West Area of the Hanford site were investigated. The most striking finding was that iodate (IO₃^-) was the most abundant species. Unexpectedly, iodide (I^-), which was likely the form of iodine in the source materials and the expected dominant groundwater species based on thermodynamic considerations, only accounted for 1-2% of the total iodine concentration. It is likely that the relatively high pH and the low abundance of sedimentary organic matter (SOM) that is present at the site slowed down or even inhibited the reduction of iodate, as SOM abiotically reduce iodate into iodide. Moreover, a study on the kinetics of iodide and iodate uptake and aqueous speciation transformation by three representative subsurface Hanford sediments was performed over a period of about one month. This study was carried out by using iodide-125 or iodate-125 at the ambient iodine-127concentration found at the site. Iodate K_d values

Molecular environment of stable iodine and radioiodine (129I) in natural organic matter: Evidence inferred from NMR and binding experiments at environmentally relevant concentrations

Science.gov (United States)

Xu, Chen; Zhong, Junyan; Hatcher, Patrick G.; Zhang, Saijin; Li, Hsiu-Ping; Ho, Yi-Fang; Schwehr, Kathleen A.; Kaplan, Daniel I.; Roberts, Kimberly A.; Brinkmeyer, Robin; Yeager, Chris M.; Santschi, Peter H.

2012-11-01

129I is a major by-product of nuclear fission and had become one of the major radiation risk drivers at Department of Energy (DOE) sites. 129I is present at elevated levels in the surface soils of the Savannah River Site (SRS) F-Area and was found to be bound predominantly to soil organic matter (SOM). Naturally bound 127I and 129I to sequentially extracted humic acids (HAs), fulvic acids (FAs) and a water extractable colloid (WEC) were measured in a 129I-contaminated wetland surface soil located on the SRS. WEC is a predominantly colloidal organic fraction obtained from soil re-suspension experiments to mimic the fraction that may be released during groundwater exfiltration, storm water or surface runoff events. For the first time, NMR techniques were applied to infer the molecular environment of naturally occurring stable iodine and radioiodine binding to SOM. Iodine uptake partitioning coefficients (Kd) by these SOM samples at ambient iodine concentrations were also measured and related to quantitative structural analyses by 13C DPMAS NMR and solution state 1H NMR on the eight humic acid fractions. By assessing the molecular environment of iodine, it was found that it was closely associated with the aromatic regions containing esterified products of phenolic and formic acids or other aliphatic carboxylic acids, amide functionalities, quinone-like structures activated by electron-donating groups (e.g., NH2), or a hemicellulose-lignin-like complex with phenyl-glycosidic linkages. However, FAs and WEC contained much greater concentrations of 127I or 129I than HAs. The contrasting radioiodine contents among the three different types of SOM (HAs, FAs and WEC) suggest that the iodine binding environment cannot be explained solely by the difference in the amount of their reactive binding sites. Instead, indirect evidence indicates that the macro-molecular conformation, such as the hydrophobic aliphatic periphery hindering the active aromatic cores and the hydrophilic

LITERATURE SURVEY FOR GROUNDWATER TREATMENT OPTIONS FOR NITRATE IODINE-129 AND URANIUM 200-ZP-1 OPERABLE UNIT HANFORD SITE

Energy Technology Data Exchange (ETDEWEB)

BYRNES ME

2008-06-05

This literature review presents treatment options for nitrate, iodine-129, and uranium, which are present in groundwater at the 200-ZP-I Groundwater Operable Unit (OU) within the 200 West Area of the Hanford Site. The objective of this review is to determine available methods to treat or sequester these contaminants in place (i.e., in situ) or to pump-and-treat the groundwater aboveground (i.e., ex situ). This review has been conducted with emphasis on commercially available or field-tested technologies, but theoretical studies have, in some cases, been considered when no published field data exist. The initial scope of this literature review included only nitrate and iodine-I 29, but it was later expanded to include uranium. The focus of the literature review was weighted toward researching methods for treatment of nitrate and iodine-129 over uranium because of the relatively greater impact of those compounds identified at the 200-ZP-I OU.

LITERATURE SURVEY FOR GROUNDWATER TREATMENT OPTIONS FOR NITRATE, IODINE-129 AND URANIUM 200-ZP-1 OPERABLE UNIT, HANFORD SITE

International Nuclear Information System (INIS)

BYRNES ME

2008-01-01

This literature review presents treatment options for nitrate, iodine-129, and uranium, which are present in groundwater at the 200-ZP-I Groundwater Operable Unit (OU) within the 200 West Area of the Hanford Site. The objective of this review is to determine available methods to treat or sequester these contaminants in place (i.e., in situ) or to pump-and-treat the groundwater aboveground (i.e., ex situ). This review has been conducted with emphasis on commercially available or field-tested technologies, but theoretical studies have, in some cases, been considered when no published field data exist. The initial scope of this literature review included only nitrate and iodine-I 29, but it was later expanded to include uranium. The focus of the literature review was weighted toward researching methods for treatment of nitrate and iodine-129 over uranium because of the relatively greater impact of those compounds identified at the 200-ZP-I OU

Long-term studies on the leachability of cemented and non-cemented iodine-129 loaded sorption material

International Nuclear Information System (INIS)

Kaempffer, R.; Furrer, J.

1989-01-01

Leaching tests on the load AC 6120 iodine sorption material (12 wt.% Ag) in water and salt brines were performed over a rather long period of time to allow better judgement of the behavior of radioactive waste disposed of in a salt dome. The utilization of capacity of the loaded iodine sorption material from the Karlsruhe reprocessing plant (WAK) was 95% related to the amount of silver added. The result of the stationary leaching tests has been a leaching rate of the material not embedded in cement of < 0.1%, whereas the leaching rate of the iodine sorption material embedded in cement has been < 0.01% of the total iodine-129 inventory. After addition of carbon steel to the sorption material embedded in cement the same leaching rates were measured as for material not embedded in cement. The addition of stainless steel exerted but little influence on the leaching rate. (orig.)

Assessment of iodine in the diet of people living around a nuclear reprocessing plant. Dose-related consequences of an intake of 129I

International Nuclear Information System (INIS)

Le Guen, B.; Berard, P.; Malarbet, J.L.; Exmelin, L.; Royer, P.

2000-01-01

It is important that in radioiodine dosimetry for low levels of daily intake, allowance must be made for the normal daily intake of stable iodine. This intake varies from one region to another, and variations are observed from one person to the next within a region, depending on eating habits. Measuring iodine in the urine over 24 hours can indirectly assess these variations. Analysis of the total iodine in the urine was carried out for 69 French people living in a temperate maritime region on in mainland France. This study justifies individual assessment of the coefficient of iodine transfer to the thyroid by means of this survey based on the urinary iodine analysis. The consequences for man of the release of 129 I around a nuclear reprocessing plant were analyzed by applying the methodology published previously by the authors. A software program based on the iodine biokinetic model recommended by the ICRP was used to calculate the daily urine excretion of 129 I for five different diets of total iodide in a ratio of 10 -4 for 129 I/ 127 I. This model makes it possible to set a practical detection limit of 20 mBq (0.003 μg). This approach is important from a practical point of view for health physicists involved in routine monitoring of workers in the nuclear field and members of the public exposed to radioiodine released into the environment. (author)

Iodine-129 in the environment of a nuclear fuel reprocessing plant by neutron activation analysis

International Nuclear Information System (INIS)

Anderson, T.J.

1978-01-01

129 I has been analyzed in both aqueous and soil samples to characterize the environmental impact of the Savannah River Plant (SRP) reprocessing operations. 129 I was quantified by a neutron activation procedure with γ-ray spectrometric detection [Ge(Li)]. For many samples, natural iodine ( 127 I) was also quantified. A wide range of samples can be accommodated by a combustion-based preirradiation isolation technique. 129 I amounts as low as 3.8 fCi can be determined with counting times of less than 30 minutes (s/sub rel/ = 10%). Deposition of 129 I in the environment via aqueous and airborne emissions has been studied. Data from analysis of seepage basin contents, spring water, on-plant streams, and the Savannah River show that 129 I from the seepage basins migrates easily through the soil with the groundwater, eventually reaching the Savannah River. Annual aqueous release rates were estimated to be 16 to 27 mCi/year. Data from analysis of soils from distances up to 159 km from SRP show above background levels of 129 I in both the minimum and maximum airborne transport directions. The soil results are compared with a wind dispersion model. The vertical distribution of 129 I in the soil was determined to a depth of 61 cm

Speciation and migration of 129I in soil profiles

International Nuclear Information System (INIS)

Luo, Maoyi; Hou, Xiaolin; Zhou, Weijian; He, Chaohui; Chen, Ning; Liu, Qi; Zhang, Luoyuan

2013-01-01

A method has been developed for speciation analysis of ultra low level 129 I in soil using sequential extraction combined with coprecipitation for separation of carrier free iodine and AMS measurement of 129 I. Two loess profiles collected from northwest China were analyzed for species of 129 I and 127 I. Similar partitioning of 129 I and 127 I was observed in the loess profiles, the distribution of iodine isotopes followed an order of organic > leachable > reducible > residue. The 129 I concentrations and 129 I/ 127 I ratios decreased exponentially with the depth, and 2 orders of magnitude lower in the deepest layer (60 and 90 cm) compared with the top layer, indicating a significant contribution of anthropogenic input in the upper layer, and high retention of 129 I in soil. The mobility of 129 I in different fractions decreased in an order of leachable > organic > oxides > residue. The results suggest that migration of iodine downwards in the soil profile is a slow process; the oxides and residue are the less mobile fractions of iodine. Highlights: ► 129 I concentration decreases exponentially with the depth of soil profile. ► The mobility of 129 I in fractions decreases: leachable > organic > oxides > residue. ► Iodine shows less mobility in oxides and residue fractions. ► High organic soil content can effectively reduce the migration of 129 I in the environment. ► Carrier free iodine AMS is an effective method for natural 129 I speciation analysis in the environment

Chemical speciation analysis and environmental behaviour of 127I and 129I

Energy Technology Data Exchange (ETDEWEB)

Hansen, Violeta

2011-10-15

a lower adsorption capacity of inorganic and organic iodine species. Adsorption of iodine species onto activated charcoal and DEAE 32 cellulose from seawater samples shows that only about 10% of the total iodine in seawater can be adsorbed onto those materials. Adsorption of iodine species from water samples onto activated charcoal/DEAE is not a suitable method for quantifying the total iodine in freshwater and seawater. An investigation was conducted in order to decompose organic iodine using K{sub 2}S{sub 2}O{sub 8} in water samples for developing a method for quantification of aquatic organic iodine (129I and 127I). The results show that iodine was quantitatively removed even when the concentration of organic iodine compounds in the studied sample was very high. Due to this, oxidation of iodine organic matter by using K{sub 2}S{sub 2}O{sub 8} followed by reduction of iodine species and precipitation with silver can be a potential method for determination of total iodine in fresh water samples. An improvement was made of the method for 129I and 127I speciation analysis in soil and sediment samples involving the extraction and fractionation of organic matter. The improved method was further used for the partitioning of 127I and 129I in marine sediments and soils. Sequential extraction results point out that partitioning of 127I and 129I within the organic fraction in soil and marine sediments is controlled by pH conditions where pH values below 5.0-5.5 promote occurrence of 127I and 129I in the humic acid, while at pH > 6 the partitioning was in the fulvic acid fraction. Anoxic conditions seemed to increase the mobility and availability of iodine compared to oxic, while suboxic conditions (soils) reduced the availability of the water soluble fraction compared to the subaqueous (marine) one. The distribution of 129I/127I values differed significantly between phases and samples, indicating that equilibrium with stable iodine have not yet been reached for a large

Femtosecond Time-Resolved Resonance-Enhanced CARS of Gaseous Iodine at Room Temperature

International Nuclear Information System (INIS)

He Ping; Fan Rong-Wei; Xia Yuan-Qin; Yu Xin; Chen De-Ying; Yao Yong

2011-01-01

Time-resolved resonance-enhanced coherent anti-Stokes Raman scattering (CARS) is applied to investigate molecular dynamics in gaseous iodine. 40 fs laser pulses are applied to create and monitor the high vibrational states of iodine at room temperature (corresponding to a vapor pressure as low as about 35 Pa) by femtosecond time-resolved CARS. Depending on the time delay between the probe pulse and the pump/Stokes pulse pairs, the high vibrational states both on the electronically ground states and the excited states can be detected as oscillations in the CARS transient signal. It is proved that the femtosecond time-resolved CARS technique is a promising candidate for investigating the molecular dynamics of a low concentration system and can be applied to environmental and atmospheric monitoring measurements. (condensed matter: electronic structure, electrical, magnetic, and optical properties)

Iodine in soil

International Nuclear Information System (INIS)

Johanson, Karl Johan

2000-12-01

A literature study of the migration and the appearance of iodine isotopes in the bio-sphere particularly in soil is presented. Some important papers in the field of iodine appearance in soil and the appearance of 129 I in the surroundings of reprocessing plants are discussed. The most important conclusions are: 1. Iodine binds to organic matter in the soil and also to some oxides of aluminium and iron. 2. If the iodine is not bound to the soil a large fraction of added 129 I is volatilized after a rather short period. 3. The binding and also the volatilisation seems to be due to biological activity in the soil. It may take place within living microorganisms or by external enzymes excreted from microorganisms. 4. Due to variations in the composition of soil there may be a large variation in the distribution of 129 I in the vertical profile of soil - usually most of the 129 I in the upper layer - which also results in large variations in the 129 I uptake to plants

Iodine in soil

Energy Technology Data Exchange (ETDEWEB)

Johanson, Karl Johan [Swedish Univ. of Agricultural Sciences, Uppsala (Sweden). Dept. of Forest Mycology and Pathology

2000-12-01

A literature study of the migration and the appearance of iodine isotopes in the bio-sphere particularly in soil is presented. Some important papers in the field of iodine appearance in soil and the appearance of {sup 129}I in the surroundings of reprocessing plants are discussed. The most important conclusions are: 1. Iodine binds to organic matter in the soil and also to some oxides of aluminium and iron. 2. If the iodine is not bound to the soil a large fraction of added {sup 129}I is volatilized after a rather short period. 3. The binding and also the volatilisation seems to be due to biological activity in the soil. It may take place within living microorganisms or by external enzymes excreted from microorganisms. 4. Due to variations in the composition of soil there may be a large variation in the distribution of {sup 129}I in the vertical profile of soil - usually most of the {sup 129}I in the upper layer - which also results in large variations in the {sup 129}I uptake to plants.

Studies of dynamic and static leaching of cemented and uncemented sorption material loaded with iodine-129

International Nuclear Information System (INIS)

Furrer, J.

1989-05-01

Leaching tests with water and brines were conducted on AC 6120 iodine sorption material (12 wt.% Ag) in order to improve the assessment of the behaviour of radioactive waste stored in a repository mine (salt or iron ore). As a result of the dynamic and static leaching tests, the leached fraction of I-129 in the uncemented material was found to be -1 %, while that of the cemented iodine sorption material was found to be -2 %. After ordinary steel had been added to the cemented sorption material, the leached fractions found were identical to those measured in uncemented material. The addition of stainless steel had only little influence on the leached fraction. (author)

Determination of low specific activity iodine-129 off-gas concentrations by GC separation and negative ionization mass spectrometry

International Nuclear Information System (INIS)

Fernandez, S.J.; Rankin, R.A.; McManus, G.J.; Nielsen, R.A.; Delmore, J.E.; Hohorst, F.A.; Murphy, L.P.

1983-09-01

This document is the final report of the laboratory development of a method for determining the specific activity of the 129 I emitted from a nuclear fuel reprocessing plant. The technique includes cryogenic sample collection, chemical form separation, quantitation by gas chromatography, and specific activity measurement of each chemical species by negative ionization mass spectrometry. The major conclusions were that both organic and elemental iodine can be quantitatively collected without fractionation and that specific activity measurements as low as one atom of 129 I per 10 5 atoms of 127 I are possible

Radioactive Iodine and Krypton Control for Nuclear Fuel Reprocessing Facilities

Directory of Open Access Journals (Sweden)

Nick R. Soelberg

2013-01-01

Full Text Available The removal of volatile radionuclides generated during used nuclear fuel reprocessing in the US is almost certain to be necessary for the licensing of a reprocessing facility in the US. Various control technologies have been developed, tested, or used over the past 50 years for control of volatile radionuclide emissions from used fuel reprocessing plants. The US DOE has sponsored, since 2009, an Off-gas Sigma Team to perform research and development focused on the most pressing volatile radionuclide control and immobilization problems. In this paper, we focus on the control requirements and methodologies for 85Kr and 129I. Numerous candidate technologies have been studied and developed at laboratory and pilot-plant scales in an effort to meet the need for high iodine control efficiency and to advance alternatives to cryogenic separations for krypton control. Several of these show promising results. Iodine decontamination factors as high as 105, iodine loading capacities, and other adsorption parameters including adsorption rates have been demonstrated under some conditions for both silver zeolite (AgZ and Ag-functionalized aerogel. Sorbents, including an engineered form of AgZ and selected metal organic framework materials (MOFs, have been successfully demonstrated to capture Kr and Xe without the need for separations at cryogenic temperatures.

Analysis of ¹²⁹I and its Application as Environmental Tracer

DEFF Research Database (Denmark)

Hou, Xiaolin; Hou, Yingkun

2012-01-01

, and highlights the progress of these analytical methods for chemical separation and sensitive measurement of 129I. The naturally occurred 129I has been used for age dating of samples/events in a range of 2-80 Ma. For the purpose of this study, an initial value of 129I has to be measured. Some progress......Iodine-129, the long-lived radioisotope of iodine, occurs naturally, but anthropogenic generated 129I has dominated the environment in the past 60 years. Due to active chemical and environmental properties of iodine and the enhanced analytical capacity for 129I measurement, the application of 129I...

Optimisation of the measurement protocols of 129I and 129I/127I. Methodology establishment for the measurement in environmental matrices

International Nuclear Information System (INIS)

Frechou, C.

2000-01-01

129 I, is a natural long-lived isotope, with a half-life of 15,7 million years, also artificially produced in nuclear power plant. It is then released in the liquid and gaseous effluents of the nuclear fuel reprocessing plants. 129 I is integrated in all biological compartments at different activity levels, depending on their distance from the emission source and their ability to metabolize iodine. Performances of the different 129 I and 129 I/ 127 I measurement techniques available: Radiochemical Neutron Activation Analysis, Accelerator Mass Spectrometry, direct γ-X spectrometry and liquid scintillation were evaluated. Associated radiochemical preparation steps of the two first techniques were optimized and adapted to the characteristics of the major environmental matrices. In a first step, the radiochemical protocols were developed and validated. In a second step, intercomparison exercises have been lead on various environmental samples presenting different 129 I activity levels. They showed the good agreement between the results given by the three techniques on different environmental matrices with activities between 0,2 and 200 Bq.kg -1 dry weight. As a conclusion, a methodology for the measurement of 129 I and 129 I/ 127 I ratio in environmental samples is proposed. It includes a decisional diagram taking into account the characteristics of the matrices, the detection limits and the answer delay. A study on the losses of 129 I during the calcination of an algae was lead by direct γ-X spectrometry and application studies were made to measure 129 I levels in different biological compartments issued from various locations: 129 I activity interspecific variation in different species of seaweeds from the French channel coast under the relative influence of La Hague, 129 I levels in bovine thyroids from the Cotentin area and 129 I in vegetal samples collected around the nuclear reprocessing plant of Marcoule. (author)

Iodine-129 measurements in soil samples from Dolon village near the Semipalatinsk nuclear test site.

Science.gov (United States)

Endo, Satoru; Tomita, Junpei; Tanaka, Kenichi; Yamamoto, Masayoshi; Fukutani, Satoshi; Imanaka, Tetsuji; Sakaguchi, Aya; Amano, Hikaru; Kawamura, Hidehisa; Kawamura, Hisao; Apsalikov, Kazbek N; Gusev, Boris I; Whitehead, Neil E; Shinkarev, Sergey; Hoshi, Masaharu

2008-07-01

Dolon village, located about 60 km from the border of the Semipalatinsk nuclear test site, is known to be heavily contaminated by the first USSR atomic bomb test in August 1949. Soil samples around Dolon were taken in October 2005 in an attempt to evaluate internal thyroid dose arising from incorporation of radioiodine isotopes (mainly (131)I). Iodine-129 in soil was measured by using the technique of accelerator mass spectrometry. The (129)I/(127)I atom ratios measured were in the range from 3.3 x 10(-9) to 3.3 x 10(-7). These values were within the range of the current background level ( approximately 10(-9) to 10(-7)) in the environment, including contributions from the global fallout of atmospheric nuclear tests and local fallout of nuclear facilities. The (129)I atom accumulated level in soil ranged from 1.28 x 10(13) to 1.59 x 10(14) atoms m(-2), the average (8.0 x 10(13)) of which was higher than the background level of (2-5) x 10(13). From the relationship between (129)I and( 137)Cs (corrected for background and decay from 1949 to 2005) accumulated levels, the background level of (129)I and the (129)I/(137)Cs ratio around Dolon were estimated to be (6.4 +/- 0.4) x 10(13) atoms m(-2) and 0.25 +/- 0.16, respectively. This (129)I/(137)Cs ratio is almost similar to the fission yield ratio for (239)Pu fast fission (0.24).

Iodine-129 depth profiles in soil within 30 km from Fukushima Daiichi Nuclear Power Plant

International Nuclear Information System (INIS)

Honda, M.; Matsuzaki, H.; Tsuchiya, Y.S.; Nakano, C.; Yamagata, T.; Nagai, H.; Matsushi, Y.; Maejima, Y.

2013-01-01

Iodine-129 depth profiles of 13 soil cores were analyzed by AMS to evaluate the distribution and the mobility in soil. The cores were sampled from various fields around the Fukushima Daiichi Nuclear Power Plant (FDNPP). Four cores out of the 13 were collected from almost the same position in Kawauchi village crop field 20 km apart from FDNPP at different times between April 2011 and June 2012 to observe the temporal variation of depth profile of "1"2"9I in soil. On the all of 13 soil cores, clear enhancement of the accident origin "1"2"9I was observed. From the crop field soil cores in Kawauchi village, "1"2"9I inventory was estimated as 43.4±2.7 mBq m"-"2 (3.10x10"1"3 atoms m"-"2). There is positive relationship between relaxation length and the elapsed time since the FDNPP accident. The increase rate of the relaxation length is about 1 cm yr"-"1 which should reflect the downward transfer rate of the Fukushima-derived "1"2"9I. Other 9 cores were collected from various fields including crop fields and man-made soils within 30 km from FDNPP on June 2012. Cumulative "1"2"9I inventory fraction [%] from the surface was calculated. The inventory fraction within top 5 cm varied widely, 65-100% with median 82%. Similarly the inventory fraction within top 10 cm varied 82 to 100% with the median 95%. (author)

A Literature Survey to Identify Potentially Volatile Iodine-Bearing Species Present in Off-Gas Streams

Energy Technology Data Exchange (ETDEWEB)

Bruffey, S. H. [Oak Ridge National Lab. (ORNL), Oak Ridge, TN (United States); Spencer, B. B. [Oak Ridge National Lab. (ORNL), Oak Ridge, TN (United States); Strachan, D. M. [Strata-G, Knoxville, TN (United States); Jubin, R. T. [Oak Ridge National Lab. (ORNL), Oak Ridge, TN (United States); Soelberg, N. R. [Idaho National Lab. (INL), Idaho Falls, ID (United States); Riley, B. J. [Pacific Northwest National Lab. (PNNL), Richland, WA (United States)

2015-06-30

Four radionuclides have been identified as being sufficiently volatile in the reprocessing of nuclear fuel that their gaseous release needs to be controlled to meet regulatory requirements (Jubin et al. 2011, 2012). These radionuclides are 3H, 14C, 85Kr, and 129I. Of these, 129I has the longest half-life and potentially high biological impact. Accordingly, control of the release of 129I is most critical with respect to the regulations for the release of radioactive material in stack emissions. It is estimated that current EPA regulations (EPA 2010) would require any reprocessing plant in the United States to limit 129I release to less than 0.05 Ci/MTIHM for a typical fuel burnup of 55 gigawatt days per metric tonne (GWd/t) (Jubin 2011). The study of inorganic iodide in off-gas systems has been almost exclusively limited to I2 and the focus of organic iodide studies has been CH3I. In this document, we provide the results of an examination of publically available literature that is relevant to the presence and sources of both inorganic and organic iodine-bearing species in reprocessing plants. We especially focus on those that have the potential to be poorly sequestered with traditional capture methodologies. Based on the results of the literature survey and some limited thermodynamic modeling, the inorganic iodine species hypoiodous acid (HOI) and iodine monochloride (ICl) were identified as potentially low-sorbing iodine species that could present in off-gas systems. Organic species of interest included both short chain alkyl iodides such as methyl iodide (CH3I) and longer alkyl iodides up to iodododecane (C10H21I). It was found that fuel dissolution may provide conditions conducive to HOI formation and has been shown to result in volatile long-chain alkyl iodides, though these may not volatilize until later in the reprocessing sequence. Solvent extraction processes were found to be significant sources of various organic iodine-bearing species; formation of these

Behavior of iodine in the atmosphere-soil-plant system

International Nuclear Information System (INIS)

Muramatsu, Yasuyuki; Yoshida, Satoshi; Uchida, Shigeo

1996-01-01

Levels and behavior of radioactive and stable iodine in the environment have been studied to obtain parameter values for the assessment of 129 I released from nuclear facilities. The deposition velocity (V D ) of gaseous iodine from the atmosphere to rice grains (rough rice) was 0.00048 cm 3 g -1 s -1 for CH 3 I and 0.15 cm 3 g -1 s -1 for I 2 . The ratio of the iodine distribution in a grain exposed to CH 3 I was as follows, rough rice : brown rice (hulled rice) : polished rice = 1.0 : 0.49 : 0.38. The distribution ratio in polished rice for CH 3 I was about 20 times higher than that for I 2 . The soil-solution distribution coefficient (K d ) for both I - and IO 3 - varied very widely, i.e. -1 . High values were found in soils having high concentrations of total organic carbon, active-Al and active-Fe (Al and Fe extracted by a mixture of oxalic acid and ammonium oxalate). Andosol, one of the most typical Japanese soils derived from deposits of volcanic ash, showed specifically high K d values. The soil-to-plant transfer factors (or concentration ratio) in the edible parts of crops were in the range 0.0002-0.016. The transfer factors for tomato, sweet potato, carrot, soybeans and rice were significantly lower than their leaf values. The value for rice (polished) was 0.002. Iodine was found to be evaporated from the soil-plant system as CH 3 I. The emission of CH 3 I from rice plants grown on flooded soil was much higher than that from oat plants grown on unflooded soil. The 129 I levels in environmental samples collected in and around Tokai-mura, where a spent nuclear fuel reprocessing plant is located, have been determined by neutron activation analysis. The concentrations of 129 I in surface soils ranged from -1 . The 129 I concentrations in forest soil tended to be higher than those in field soils. Most of the 129 I was retained in the first 10 cm of the surface soil collected from forests in Tokai-mura. (author)

RETROSPECTIVE RECONSTRUCTION OF INTEGRAL IODINE-131 FALLOUT FOR THE SETTLEMENTS OF THE BRYANSK REGION OF RUSSIA ON THE BASIS OF RESULTS OF IODINE-129 CONTENT IN THE SOIL DETERMINATION IN 2008

Directory of Open Access Journals (Sweden)

Yu. I. Gavrilin

2009-01-01

Full Text Available The article briefly describes the procedure of reconstruction of integral iodine-131 fallouts using fragmentary data on iodine-131 fallouts in May-June 1986, as well as results of determination (in the late period after the accident of iodine-129 concentration in the soil and values of integral fallouts of cesium-137 in the settlements of the Bryansk region of Russia. Results of estimation of integral iodine-131 fallouts (in the area of 32 soil sampling points are presented in the table form. Regularities of ratio (131I/137CsII change in the integral radionuclide fallouts are being determined and values of integral iodine-131 fallouts are being estimatedfor the other settlements of the region with the known values of integral cesium-137 fallouts. It is shown that variability of the average for settlements values of integral iodine-131 fallouts is 70 times less then variability of corresponding integral cesium-137 fallouts.

Determination of low specific activity iodine-129 off-gas concentrations by GC separation and negative ionization mass spectrometry

Energy Technology Data Exchange (ETDEWEB)

Fernandez, S.J.; Rankin, R.A.; McManus, G.J.; Nielsen, R.A.; Delmore, J.E.; Hohorst, F.A.; Murphy, L.P.

1983-09-01

This document is the final report of the laboratory development of a method for determining the specific activity of the /sup 129/I emitted from a nuclear fuel reprocessing plant. The technique includes cryogenic sample collection, chemical form separation, quantitation by gas chromatography, and specific activity measurement of each chemical species by negative ionization mass spectrometry. The major conclusions were that both organic and elemental iodine can be quantitatively collected without fractionation and that specific activity measurements as low as one atom of /sup 129/I per 10/sup 5/ atoms of /sup 127/I are possible.

The 129-iodine content of subtropical Pacific waters. Impact of Fukushima and other anthropogenic 129-iodine sources

Energy Technology Data Exchange (ETDEWEB)

Guilderson, T.P. [Lawrence Livermore National Laboratory, Livermore, CA (United States). Center for Accelerator Mass Spectrometry; California Univ., Santa Cruz, CA (United States). Dept. of Ocean Sciences and Inst. of Marine Sciences; Tumey, S.J.; Brown, T.A. [Lawrence Livermore National Laboratory, Livermore, CA (United States). Center for Accelerator Mass Spectrometry; Buesseler, K.O. [Woods Hole Oceanographic Institution, Woods Hole, MA (United States). Dept. of Marine Chemistry and Geochemistry

2014-07-01

Results obtained from a dedicated radiochemistry cruise approximately 100 days after the 11 March 2011 Tohoku earthquake and subsequent disaster at the Fukushima Daiichi Nuclear Power Plant show that Fukushima derived radionuclides in the nearby ocean environment had penetrated, on average, to ≤250 m depth (1026.5 kg m{sup 3} potential density surface). The excess inventory of Fukushima-derived {sup 129}I in the region (∝150 000 km{sup 2}) sampled during the cruise is estimated to have been between 0.89 and 1.173 billion Bq (∝136 to ∝179 grams) of {sup 129}I. Based on a tight tracer-tracer relation with {sup 134}Cs (or {sup 137}Cs) and estimates that most of the excess cesium is due to direct discharge, we infer that much of the excess {sup 129}I is from direct (non-atmospheric deposition) discharge. After taking into account oceanic transport, we estimate the direct discharge, i.e., that directly released into the ocean, off Fukushima to have been ∝1 kg {sup 129}I. Although this small pulse is dwarfed by the ∝90 kg of weapons-testing-derived {sup 129}I that was released into the environment in the late 1950s and early 1960s, it should be possible to use Fukushima-derived {sup 129}I and other radionuclides (e.g., {sup 134,} {sup 137}Cs) to study transport and entrainment processes along and across the Kuroshio Current.

Health effects due to the release of iodine 129 from the marine outlet for the reprocessing plant located at La Hague

International Nuclear Information System (INIS)

Robeau, D.; Calmet, D.

1985-02-01

The study contained in this report estimates the health effects in terms of doses to the populations due to the release of Iodine 129 from the marine outlet for the reprocessing plant located at La Hague. The release taken into account is due to the normal functioning of the plant, which introduces a consistent contamination of the English channel during the life of the plant which is thirty years. The annual release of Iodine 129, as assumed by the operating staff, is equal to either 1,662.10 12 Bq or 45 Ci. The dose equivalent to the thyroid of the concerned population due to normal consummation of marine products (fish, shell-fish, mollusc) are very low as compared to the 6.10 -4 limit of dose authorized for the public in the actual regulation. The effective dose equivalent has been estimated at 4.27.10 -7 Sv [fr

Determination of iodine to compliment mass spectrometric measurements

International Nuclear Information System (INIS)

Hohorst, F.A.

1994-11-01

The dose of iodine-129 to facility personnel and the general public as a result of past, present, and future activities at DOE sites is of continuing interest, WINCO received about 160 samples annually in a variety of natural matrices, including snow, milk, thyroid tissue, and sagebrush, in which iodine-129 is determined in order to evaluate this dose, Currently, total iodine and the isotopic ratio of iodine-127 to iodine-129 are determined by mass spectrometry. These two measurements determine the concentration of iodine-129 in each sample, These measurements require at least 16 h of mass spectrometer operator time for each sample. A variety of methods are available which concentrate and determine small quantities of iodine. Although useful, these approaches would increase both time and cost. The objective of this effort was to determine total iodine by an alternative method in order to decrease the load on mass spectrometry by 25 to 50%. The preparation of each sample for mass spectrometric analysis involves a common step--collection of iodide on an ion exchange bed. This was the focal point of the effort since the results would be applicable to all samples

Volatilization of iodine from vegetation

International Nuclear Information System (INIS)

Amiro, B.D.; Johnston, F.L.

1989-01-01

Gaseous emissions of iodine were measured from bean plant foliage. A gamma-emitting iodine tracer, Na 125 I, was taken up by the plants from a hydroponic growth medium and released to a cuvette atmosphere. The dynamics of the flux were studied using a flow-through gamma detector. The relationship between leaf radioactive tracer activity and growth-medium activity was linear, as was the relationship between the iodine flux and both leaf and growth-medium activity. Iodine flux and leaf conductance to water responded similarly to changes in light levels, suggesting that the stomata may partially control the flux. The flux was inhibited by aeration of the hydroponic growth media, and we postulate that methylation causes the iodine flux. Iodine emissions from living vegetation probably contribute < 0.1% to the stable iodine concentration in the atmosphere above terrestrial areas. However, this pathway may be a direct route for radioactive iodine transport from contaminated soils to the atmosphere. (author)

Volatilization of iodine from vegetation

Energy Technology Data Exchange (ETDEWEB)

Amiro, B D; Johnston, F L [Atomic Energy of Canada Ltd., Pinawa, MB (Canada). Whiteshell Nuclear Research Establishment

1989-01-01

Gaseous emissions of iodine were measured from bean plant foliage. A gamma-emitting iodine tracer, Na {sup 125}I, was taken up by the plants from a hydroponic growth medium and released to a cuvette atmosphere. The dynamics of the flux were studied using a flow-through gamma detector. The relationship between leaf radioactive tracer activity and growth-medium activity was linear, as was the relationship between the iodine flux and both leaf and growth-medium activity. Iodine flux and leaf conductance to water responded similarly to changes in light levels, suggesting that the stomata may partially control the flux. The flux was inhibited by aeration of the hydroponic growth media, and we postulate that methylation causes the iodine flux. Iodine emissions from living vegetation probably contribute < 0.1% to the stable iodine concentration in the atmosphere above terrestrial areas. However, this pathway may be a direct route for radioactive iodine transport from contaminated soils to the atmosphere. (author).

Immobilisation of fission iodine by reaction with insoluble natural organic matter

International Nuclear Information System (INIS)

Schmett, G.T.; Kimble, G.M.; Steinberg, S.M.; Emerson, D.W.; Cerefice, G.S.

2005-01-01

Commercial nuclear power plants produce Iodine-129 ( 129 I) as a fission by-product. Iodine-129, along with other stable isotopes of iodine, is released during the reprocessing of nuclear fuel. Silver-impregnated activated carbon, activated carbon, cinnabar and chalcocite have been used in the past to remove iodide and iodine from waste streams. There is environmental and geological evidence that iodine can become associated with natural organic matter (NOM). For example, a number of previous studies have shown that iodine (including 129 I) can be strongly retained in organic-rich surface soils and humic material. This research explores the use of NOM (sphagnum peat) to sequester iodine from acid vapour and aqueous solution. NOM may be stable for geological storage or the sequestered iodine can be recovered to prepare target materials for transmutation. The nature of the sphagnum iodine association has been explored as well as method that can be used to concentrate and recover sequestered iodine from the peat moss. (authors)

Iodine oxides in large-scale THAI tests

International Nuclear Information System (INIS)

Funke, F.; Langrock, G.; Kanzleiter, T.; Poss, G.; Fischer, K.; Kühnel, A.; Weber, G.; Allelein, H.-J.

2012-01-01

Highlights: ► Iodine oxide particles were produced from gaseous iodine and ozone. ► Ozone replaced the effect of ionizing radiation in the large-scale THAI facility. ► The mean diameter of the iodine oxide particles was about 0.35 μm. ► Particle formation was faster than the chemical reaction between iodine and ozone. ► Deposition of iodine oxide particles was slow in the absence of other aerosols. - Abstract: The conversion of gaseous molecular iodine into iodine oxide aerosols has significant relevance in the understanding of the fission product iodine volatility in a LWR containment during severe accidents. In containment, the high radiation field caused by fission products released from the reactor core induces radiolytic oxidation into iodine oxides. To study the characteristics and the behaviour of iodine oxides in large scale, two THAI tests Iod-13 and Iod-14 were performed, simulating radiolytic oxidation of molecular iodine by reaction of iodine with ozone, with ozone injected from an ozone generator. The observed iodine oxides form submicron particles with mean volume-related diameters of about 0.35 μm and show low deposition rates in the THAI tests performed in the absence of other nuclear aerosols. Formation of iodine aerosols from gaseous precursors iodine and ozone is fast as compared to their chemical interaction. The current approach in empirical iodine containment behaviour models in severe accidents, including the radiolytic production of I 2 -oxidizing agents followed by the I 2 oxidation itself, is confirmed by these THAI tests.

Bacterial contribution to iodine volatilization in the environment

Energy Technology Data Exchange (ETDEWEB)

Amachi, S; Kasahara, M; Fujii, T [Chiba Univ., Dept. of Bioresources Chemistry, Matsudo, Chiba (Japan); Muramatsu, Y [National Inst. of Radiological Sciences, Chiba (Japan)

2003-09-01

The roles of microorganisms in iodine volatilization from the environment were studied. More than 100 bacterial strains were isolated from various environments such as soils, seawater and marine sediments, and were examined their capacities for volatilizing iodine. Approximately 40% of these bacteria showed significant capacities for volatilizing iodine. Gas chromatographic determinations revealed that the chemical species of gaseous iodine is methyl iodide (CH{sub 3}I). Phylogenetic analysis based on 16S ribosomal DNA showed that these 'iodine-volatilizing bacteria' are widely distributed through the bacterial domain. The iodide-methylating reaction was mediated by an enzyme protein with S-adenosyl-L-methionine (SAM) as the methyl donor. We then estimated bacterial contribution to iodine volatilization from soils. Iodine in soils was volatilized mainly as CH{sub 3}I. CH{sub 3}I emission was enhanced in the presence of glucose or yeast extract, but was inhibited by autoclaving of soils. Little CH{sub 3}I was produced under anaerobic conditions. Furthermore, the addition of streptomycin and tetracycline, antibiotics which inhibit bacterial growth, strongly inhibited CH{sub 3}I emission, while a fungal inhibitor cycloheximide caused little effect. These results suggest that iodine in soils is volatilized as CH{sub 3}I mainly by the action of aerobic soil bacteria. Similar experiment was carried out by using sea water samples. The emission of iodine from sea waters occurred biologically, and bacterial (and also other microbial) contribution was confirmed. Our results suggest that iodine is methylated and volatilized into the atmosphere as a result of bacterial activities. Since bacteria are so abundant and widespread in the environments, they may significantly contribute to global iodine volatilization. This indicates that if {sup 129}I would be released from nuclear facilities, weapons testing or ground storage of nuclear wastes, the pathway of volatilization by

Development of iodine waste forms using low-temperature sintering glass

International Nuclear Information System (INIS)

Krumhansl, James Lee; Nenoff, Tina Maria; Garino, Terry J.; Rademacher, David

2010-01-01

This presentation will describe our recent work on the use of low temperature-sintering glass powders mixed with either AgI or AgI-zeolite to produce a stable waste form. Radioactive iodine ( 129 I, half-life of 1.6 x 10 7 years) is generated in the nuclear fuel cycle and is of particular concern due to its extremely long half-life and its effects on human health. As part of the DOE/NE Advanced Fuel Cycle Initiative (AFCI), the separation of 129 I from spent fuel during fuel reprocessing is being studied. In the spent fuel reprocessing scheme under consideration, the iodine is released in gaseous form and collected using Ag-loaded zeolites, to form AgI. Although AgI has extremely low solubility in water, it has a relatively high vapor pressure at moderate temperatures (>550 C), thus limiting the thermal processing. Because of this, immobilization using borosilicate glass is not feasible. Therefore, a bismuth oxide-based glasses are being studied due to the low solubility of bismuth oxide in aqueous solution at pH > 7. These waste forms were processed at 500 C, where AgI volatility is low but the glass powder is able to first densify by viscous sintering and then crystallize. Since the glass is not melted, a more chemically stable glass can be used. The AgI-glass mixture was found to have high iodine leach resistance in these initial studies.

Application of crown ethers to selective extraction and quantitative analysis of technetium 99, iodine 129 and cesium 135 in effluents

International Nuclear Information System (INIS)

Paviet, P.

1992-01-01

Properties of crown ethers are first recalled. Then extraction of technetium 99 is studied in actual radioactive effluents. Quantitative analysis is carried out by liquid scintillation and interference of tritium is corrected. Iodine 129 is extracted from radioactive effluents and determined by gamma spectrometry. Finally cesium 135 is extracted and determined by thermo ionization mass spectroscopy

Determination of iodine in oyster tissue by isotope dilution laser resonance ionization mass spectrometry

International Nuclear Information System (INIS)

Fassett, J.D.; Murphy, T.J.

1990-01-01

The technique of laser resonance ionization mass spectrometry has been combined with isotope dilution analysis to determine iodine in oyster tissue. The long-lived radioisotope, 129I, was used to spike the samples. Samples were equilibrated with the 129I, wet ashed under controlled conditions, and iodine separated by coprecipitation with silver chloride. The analyte was dried as silver ammonium iodide upon a tantalum filament from which iodine was thermally desorbed in the resonance ionization mass spectrometry instrument. A single-color, two-photon resonant plus one-photon ionization scheme was used to form positive iodine ions. Long-lived iodine signals were achieved from 100 ng of iodine. The precision of 127I/129I measurement has been evaluated by replicate determinations of the spike, the spike calibration samples, and the oyster tissue samples and was 1.0%. Measurement precision among samples was 1.9% for the spike calibration and 1.4% for the oyster tissue. The concentration of iodine determined in SRM 1566a, Oyster Tissue, was 4.44 micrograms/g with an estimate of the overall uncertainty for the analysis of +/- 0.12 microgram/g

Optimisation of the measurement protocols of {sup 129}I and {sup 129}I/{sup 127}I. Methodology establishment for the measurement in environmental matrices; Optimisation des protocoles de mesurage de {sup 129}I et {sup 129}I/{sup 127}I. Etablissement d'une methodologie adaptee aux echantillons de l'environnement

Energy Technology Data Exchange (ETDEWEB)

Frechou, C

2000-07-01

{sup 129}I, is a natural long-lived isotope, with a half-life of 15,7 million years, also artificially produced in nuclear power plant. It is then released in the liquid and gaseous effluents of the nuclear fuel reprocessing plants. {sup 129}I is integrated in all biological compartments at different activity levels, depending on their distance from the emission source and their ability to metabolize iodine. Performances of the different {sup 129}I and {sup 129}I/{sup 127}I measurement techniques available: Radiochemical Neutron Activation Analysis, Accelerator Mass Spectrometry, direct {gamma}-X spectrometry and liquid scintillation were evaluated. Associated radiochemical preparation steps of the two first techniques were optimized and adapted to the characteristics of the major environmental matrices. In a first step, the radiochemical protocols were developed and validated. In a second step, intercomparison exercises have been lead on various environmental samples presenting different {sup 129}I activity levels. They showed the good agreement between the results given by the three techniques on different environmental matrices with activities between 0,2 and 200 Bq.kg{sup -1} dry weight. As a conclusion, a methodology for the measurement of {sup 129}I and {sup 129}I/{sup 127}I ratio in environmental samples is proposed. It includes a decisional diagram taking into account the characteristics of the matrices, the detection limits and the answer delay. A study on the losses of {sup 129}I during the calcination of an algae was lead by direct {gamma}-X spectrometry and application studies were made to measure {sup 129}I levels in different biological compartments issued from various locations: {sup 129}I activity interspecific variation in different species of seaweeds from the French channel coast under the relative influence of La Hague, {sup 129}I levels in bovine thyroids from the Cotentin area and {sup 129}I in vegetal samples collected around the nuclear

Study on adsorption performance of coal based activated carbon to radioactive iodine and stable iodine

International Nuclear Information System (INIS)

Zhou, Junbo; Hao, Shan; Gao, Liping; Zhang, Youchen

2014-01-01

Highlights: • The impregnated coal-based activated carbons as adsorbent for removing methyl iodide. • The coal-based activated carbons to remove stable iodine. • Iodine residues are under 0.5 μg/ml after adsorption treatment. • The decontamination factor is much higher than 1000. - Abstract: Nuclear power plant, nuclear reactors and nuclear powered ship exhaust contains a large amount of gaseous radioactive iodine, and can damage to the workplace and the surrounding environment. The quantitative test to remove methyl iodide and the qualitative test for removing stable iodine were investigated using the impregnated coal-based activated carbons and coal-based activated carbons as adsorbents. The research conducted in this work shows that iodine residues were under 0.5 μg/ml after adsorption treatment and the decontamination factor of the coal-based activated carbon for removing the stable iodine was more than 1000, which can achieve the purpose of removing harmful iodine, and satisfy the requirement of gaseous waste treatment of nuclear powered vessel and other nuclear plants

Progress on ¹²⁹I analysis and its application in environmental and geological researches

DEFF Research Database (Denmark)

Fan, Yukun; Hou, Xiaolin; Zhou, Weijian

2013-01-01

of dispersion and migration of short-lived radioisotopes of iodine released from nuclear accidents. This article aims to summarize and critically compare the analytical techniques used for 129I measurement and chemical methods for separation of iodine from various sample matrices, purification from......Iodine-129 is a naturally generated isotope, but anthropogenic releases are the dominated source of 129I in the present environment. Among many measurement techniques, neutron activation analysis (NAA) and accelerator mass spectrometry (AMS) are only methods used for measurement of 129I...... in environmental level. Based on its source terms, chemical properties and environmental behaviors, 129Ican be applied for geological dating in a range of 2–80Ma, investigation of formation and migration of hydrocarbon, circulation of ocean water, atmospheric process of iodine, as well as reconstruction...

Speciation analysis of ¹²⁹I and its applications in environmental research

DEFF Research Database (Denmark)

Zhang, Luyuan; Hou, Xiaolin

2013-01-01

129I, a long-lived radionuclide, is important in view of geological repository of nuclear waste, and environmental tracing applications related to diverse natural processes of iodine. The environmental behaviors and bioavailability of 129I are highly related to its species. A number of methods have...... been reported for speciation analysis of 129I in a variety of environmental samples. These methods have been applied in many researches, including conversion processes of iodine species in marine and terrestrial systems, migration and retention of iodine in soil and sediment, geochemical cycling...

An example of transition from a corrosion process in gaseous phase to corrosion in aqueous environment: the case of Z2CN18-10 stainless steel by iodine and water in vapour phase

International Nuclear Information System (INIS)

Mathieu, Bruno

1990-01-01

This research thesis addresses an example of transition of a corrosion process in gaseous phase towards corrosion in aqueous environment, specifically in the case of the corrosion of the Z2CN18-10 stainless steel by gaseous iodine in presence of water vapour (and possibly nitrogen dioxide). This transition occurs in two steps: initiation in gaseous phase and growth in aqueous environment. This transition is due to hygroscopic properties of mostly chromium iodides and, to a lesser extent, iron iodides. Morphological, electrochemical and thermogravimetry studies have been performed by varying different parameters governing corrosion processes: corrosion temperature, iodine concentration, relative humidity, and reaction time [fr

Modelling the chemistry of iodine

International Nuclear Information System (INIS)

Paquette, J.

1989-01-01

We have assembled a kinetic model, based on elementary chemical reactions, that describes the chemical behaviour of iodine in aqueous solution as a function of time and various parameters such as pH, concentration and radiation field. The model is conceptually divided into six section: aqueous iodine chemistry, aqueous organic iodide chemistry, water radiolysis, radiolysis of iodine solutions, radiolysis of organic iodide solutions and mass transfer. The model indicates that, in the absence of a radiation field, the rate of production of volatile iodine species is controlled by the rate of oxidation of the iodide ion. The volatile iodine species are dominated by organic iodides if organic impurities are present. The single most important parameter controlling iodine volatility is the pH of the solution; high pH values tend to minimize iodine volatility. In the presence of a radiation field, the volatility of iodine is controlled by the radiation-induced oxidation of the iodide ion. Again, iodine volatility is dominated by organic iodides if organic impurities are present. High pH values minimize iodine volatility. A sensitivity analysis has been performed on some sections of the model to identify reactions to which the volatility of iodine is most sensitive. In the absence of a radiation field, the volatility is most sensitive, first, to the rate of oxidation of the iodide ion, and, second, to the rate of mass transfer of volatile species between the aqueous and the gaseous phases. This approach should be useful in identifying reactions for which accurate rate constants are required and in decreasing the complexity of the model. 37 refs

Accurate determination of 129I concentrations and 129I/137Cs ratios in spent nuclear resins by Accelerator Mass Spectrometry

International Nuclear Information System (INIS)

Nottoli, Emmanuelle; Bienvenu, Philippe; Labet, Alexandre; Bourlès, Didier; Arnold, Maurice; Bertaux, Maité

2014-01-01

Determining long-lived radionuclide concentrations in radioactive waste has fundamental implications for the long-term management of storage sites. This paper focuses on the measurement of low 129 I contents in ion exchange resins used for primary fluid purification in Pressurised Water Reactors (PWR). Iodine-129 concentrations were successfully determined using Accelerator Mass Spectrometry (AMS) following a chemical procedure which included (1) acid digestion of resin samples in HNO 3 /HClO 4 , (2) radioactive decontamination by selective iodine extraction using a new chromatographic resin (CL Resin), and (3) AgI precipitation. Measured 129 I concentrations ranged from 4 to 12 ng/g, i.e. from 0.03 to 0.08 Bq/g. The calculation of 129 I/ 137 Cs activity ratios used for routine waste management produced values in agreement with the few available data for PWR resin samples. - Highlights: • In the context of radioactive waste management, this study aimed at measuring 129 I in spent resins using accelerator mass spectrometry. • The treatment procedure included microwave acid digestion of samples, iodine extraction by CL resins and AgI precipitation. • Developed first on synthetic matrices, the chemical treatment procedure was then successfully applied to real resin samples. • 129 I concentrations ranged from 4 to 12 ng/g of dry resin. • Results are in agreement with previous measurements and support reference values currently used for nuclear resin management

Determination of 129I using distillation method and liquid scintillation spectrometry

International Nuclear Information System (INIS)

Horvathova, B.; Dulanska, S.; Remenec, B.; Matel, L.; Gardonova, V.

2014-01-01

The conditions for effective distillation of iodine as a screening method for the determination of 129 I by liquid scintillation spectrometry were optimized. By distillation of iodine it is possible to achieve high-purity fraction without interferences needed for measuring 129 I for liquid scintillation spectrometer. Yields of separation were determined gravimetrically using PdI 2 ·H 2 O. The environment that was found to be effective for distillation of iodine is made up of 1 - 2 mol dm -3 HNO 3 together with 0.4 g of NaNO 2 as an oxidizing agent (I . →I 2 ). For testing of distillation, suitable apparatus for distillation of iodine was designed. The apparatus was connected to a vacuum box, which sucks iodine of the distilled solution. Then the iodine was captured in a solution of NaOH at a concentration of 1.5 mol dm -3 . As part of the optimization methodology, it was found that the concentration of NaOH solution for adsorption I 2 (g) does not have any influence on the yields, as opposed to its volume, where it is necessary to use a maximum amount of NaOH in the holding flask for maximum adsorption of iodine. It was determined, that time needed for coagulation PdI 2 ·H 2 O is 24 hours and suitable time for distillation was 20 minutes. Optimized method for the determination of 129 I was applied for various matrices from NPPs in Slovak Republic. Values of 129 I for all analyzed samples were less than the minimum detectable activity (0.043 Bq). The separation yields were in the range (73.14 to 82.04)% and 129 I was measured on a liquid scintillation spectrometer TRI CARB 2900TR with high detection efficiency of 95%. (authors)

Determination of 129I in radioactive wastes

International Nuclear Information System (INIS)

Horvathova, B.; Dulanska, S.; Matel, L.; Remenec, B.; Gardonova, V.

2015-01-01

The goal of this work was to develop and optimize the conditions for the distillation of iodine and its use for determination of 129 I on liquid scintillation spectrometer (LSC). An appropriate distillation apparatus for distillation of iodine was proposed by testing distillation apparatus. A method of cleaning of 129 I from present interferents , e.g. 14 C, 137 Cs, was tested on proposed simple distillation apparatus. High-purity fraction needed for the determination of 129 I was achieved by distillation on liquid scintillation spectrometer TRI CARB 2900TR from Perkin Elmer Company. Optimal energy window (0 - 80) keV was chosen to measure 129 I on liquid scintillation spectrometer. Ultima Gold TM AB was chosen as more appropriate scintillator by testing of two scintillation solutions. Optimized method for determining the 129 I was applied to real samples coming from Bohunice NPP. The combination of precipitation method and method of 129 I purification by distillation is easy and less time consuming separation method for the determination of 129 I compared to conventional methods of separation of 129 I, e.g. by liquid extraction. Measuring method on the LSC spectrometer represents a measurement with a higher detection efficiency (95%) as compared to measurement of low-energy X-ray radiation 129 I (29.6 keV) with X-ray detector Si (Li) 12155 SL with detection efficiency only (1-2)%.

Deep Bed Iodine Sorbent Testing FY 2011 Report

International Nuclear Information System (INIS)

Soelberg, Nick; Watson, Tony

2011-01-01

Nuclear fission results in the production of fission products (FPs) and activation products that increasingly interfere with the fission process as their concentrations increase. Some of these fission and activation products tend to evolve in gaseous species during used nuclear fuel reprocessing. Analyses have shown that I129, due to its radioactivity, high potential mobility in the environment, and high longevity (half life of 15.7 million years), can require control efficiencies of up to 1,000x or higher to meet regulatory emission limits. Deep-bed iodine sorption testing has been done to evaluate the performance of solid sorbents for capturing iodine in off-gas streams from nuclear fuel reprocessing plants. The objectives of the FY 2011 deep bed iodine sorbent testing are: (1) Evaluate sorbents for iodine capture under various conditions of gas compositions and operating temperature (determine sorption efficiencies, capacities, and mass transfer zone depths); and (2) Generate data for dynamic iodine sorption modeling. Three tests performed this fiscal year on silver zeolite light phase (AgZ-LP) sorbent are reported here. Additional tests are still in progress and can be reported in a revision of this report or a future report. Testing was somewhat delayed and limited this year due to initial activities to address some questions of prior testing, and due to a period of maintenance for the on-line GC. Each test consisted of (a) flowing a synthetic blend of gases designed to be similar to an aqueous dissolver off-gas stream over the sorbent contained in three separate bed segments in series, (b) measuring each bed inlet and outlet gas concentrations of iodine and methyl iodide (the two surrogates of iodine gas species considered most representative of iodine species expected in dissolver off-gas), (c) operating for a long enough time to achieve breakthrough of the iodine species from at least one (preferably the first two) bed segments, and (d) post-test purging

Insights into iodine behaviour and speciation in the Phébus primary circuit

International Nuclear Information System (INIS)

Girault, N.; Payot, F.

2013-01-01

during the four Phébus-bundle tests. In these tests, the impact of different oxido-reducing and thermal– hydraulics conditions prevailing in the primary circuit as well as the impact of boron and control rod materials on iodine behaviour has been investigated. In this test series, iodine behaviour in the FPT3 primary circuit clearly departed from the others because a much higher iodine retention was observed upstream the steam generator (due to partial boron-rich blockage after 14,500 s) but above all a much higher gaseous iodine fraction in hot and cold legs was formed as compared to other tests. In the three other Phébus FP tests, iodine was generally poorly retained in the primary circuit (70% of released iodine reaching the containment vessel). Two main zones of significant deposition were identified coinciding with sections in which temperatures dropped rapidly. These were the fuel bundle exit (upper plenum and vertical line) where the gas cooled from very high fuel temperatures down to 700 °C and the steam generator riser (upstream part and hot leg entrance) where temperatures cooled from 700 °C to 150 °C. As expected, iodine was mainly transported under vapour forms in the circuit hot leg. However, Phébus FP tests provided new insights into iodine transport, as several volatile iodine vapour species not associated to caesium were evidenced. In all tests, a significant amount of iodine under a gaseous form was found in the containment early during the bundle transient phase, implying that this gas was originated from the circuit. Except for FPT3, measurements of gaseous iodine in the circuit, from discrete samplings, were however more contradictory as only negligible amounts of gaseous iodine were generally measured in the cold leg. Due to the limitations of such measurements (trapping efficiencies, limited period of samplings) the gaseous iodine occurrence in the primary circuit during FPT0/1/2 could neither be stated nor refuted. Finally, Phébus FP test

Iodine filters in nuclear installations

International Nuclear Information System (INIS)

Wilhelm, J.G.

1982-01-01

The present report discusses the significance for environmental exposure of the iodine released with the gaseous effluents of nuclear power stations and reprocessing plants in relation to releases of other airborne radionuclides. Iodine filtration processes are described. The release pathways and the composition of airborne fission product iodine mixtures and their bearing on environmental exposure are discussed on the basis of measured fission product iodine emissions. The sorbents which can be used for iodine filtration, their removal efficiencies and range of applications are dealt with in detail. The particular conditions governing iodine removal, which are determined by the various gaseous iodine species, are illustrated on the basis of experimentally determined retention profiles. Particular attention is given to the limitations imposed by temperature, humidity, radiation and filter poisoning. The types of filter normally used are described, their advantages and drawbacks discussed, the principles underlying their design are outlined and the sources of error indicated. The methods normally applied to test the efficiency of various iodine sorbents are described and assessed. Operating experience with iodine filters, gathered from surveillance periods of many years, is supplemented by a large number of test results and the findings of extensive experiments. Possible ways of prolonging the permissible service lives of iodine filters are discussed and information is given on protective measures. The various iodine removal processes applied in reprocessing plants are described and compared with reference to efficiency and cost. The latest developments in filter technology in reprocessing plants are briefly outlined

J129 in the biocycle

International Nuclear Information System (INIS)

Handl, J.; Kuehn, W.

1980-01-01

A brief survey on the few known data on the radioecological behaviour of 129 J is given. Numerous investigations as to the 129 J-uptake in the thyroid of cattle were carried out in the USA. In Western Europe, practically only in the near surroundings of nuclear-technical plants measurements of 129 J were carried out. In the author's opinion, to clarify the ecological behaviour of 129 J, human thyroids should be examined as well, in special regions the share of 129 J in milk, grass, food, and ground-near air should be determined and tests with especially important iodine compounds from various soils and plants should be carried out concerning this re-emissions. (MG) [de

Mock iodine-125 radiation source

International Nuclear Information System (INIS)

Coffey, D.L.

1976-01-01

An intimate mixture of americium-241 and iodine-129 provides an energy spectrum that reliably simulates the spectrum of iodine-125 in a well-type detector. As such, it may be used as a long-lived standard to calibrate instruments such as well scintillation spectrometers in which measurements are to be made involving iodine-125

Speciation and migration of 129I in soil profiles

DEFF Research Database (Denmark)

Luo, Maoyi; Hou, Xiaolin; Zhou, Weijian

2013-01-01

A method has been developed for speciation analysis of ultra low level 129I in soil using sequential extraction combined with coprecipitation for separation of carrier free iodine and AMS measurement of 129I. Two loess profiles collected from northwest China were analyzed for species of 129I...

Iodine-129. Proceedings of an NEA specialist meeting. Paris, 13-16 June 1977. Iode-129. Compte rendu d'une reunion de specialistes de l'AEN. Paris, 13-16 juin 1977

Energy Technology Data Exchange (ETDEWEB)

1977-01-01

In the framework of its programme on effluent releases from the nuclear fuel cycle and its radiological significance, the Committee on Radiation Protection and Public Health decided to organise meetings of specialists directly involved with research or regulatory aspects of effluent releases in order to note the status of present knowledge in this field. A first meeting of this type on iodine 129 was organised by the OECD Nuclear Energy Agency. This publication reproduces papers presented at this meeting.

Migration and inventories of iodine-129 and iodine-127 in soils; Migration und Inventare von Iod-129 und Iod-127 in Boeden

Energy Technology Data Exchange (ETDEWEB)

Daraoui, A.; Michel, R.; Gorny, M.; Jakob, D.; Sachse, R. [Leibniz Univ. Hannover (Germany). Zentrum fuer Strahlenschutz und Radiooekologie; Alfimov, V.; Synal, H.A. [Eidgenoessische Technische Hochschule (ETH), Zuerich (Switzerland)

2009-07-01

Soil profiles from Bavaria in southern Germany and from Chile were analysed for {sup 129}I by accelerator mass spectrometry (AMS) and for {sup 127}I by inductively coupled plasma mass spectrometry (ICP-MS). The deposition density of {sup 129}I in the soils from Bavaria was (109 x 1.5{sup {+-}}{sup 1}) mBq m{sup -2} (geometric mean and geometric standard deviation). The dominant sources of {sup 129}I in Bavaria are the reprocessing plants La Hague and Sellafield and not the Chernobyl fallout. The {sup 129}I/{sup 127}I isotopic ratios of the Bavarian soils were measured between 10{sup -7} and 10{sup -10}, 100- to 1000-time higher than the ratios observed for the samples from Chile. The {sup 129}I integral deposition densities in Chile, Easter Island and Antarctica were between 0.3 and 2 mBq m{sup -2}. In these soils, the observed {sup 129}I/{sup 127}I ratios were about 10{sup -12}. This value is consistent with the results from the marine sediments representing the pre-nuclear equilibrium ratios. The soils from Chile allow the determination of the {sup 129}I fallout from the atmospheric nuclear weapons explosions undisturbed from contaminations due to releases from reprocessing plants. (orig.)

Transport of Iodine Species in the Terrestrial Environment

International Nuclear Information System (INIS)

Hu, Q; Moran, J E; Zhao, P

2003-01-01

The fate and transport of iodine in the environment is of interest because of the large production and release of 129 I from anthropogenic sources. 129 I has a long half-life (1.57 x 10 7 years) and exhibits complex geochemical behavior. The main source of 129 I in the environment is from nuclear fuel reprocessing facilities; about 2,600 kg from facilities in England and France. During 1944-1972, the Hanford Site in Washington state released about 260 kg 129 I. Iodine has a unique and complex chemistry in the environment, and its fate and transport in aqueous environments is dictated by its chemical speciation. In reducing environments, aqueous iodine usually occurs as the highly mobile iodide anion (I - ). Under more oxidizing conditions, iodine may be present as the more reactive iodate anion (IO 3 - ), which could lead to retarded transport through interaction with clays and organic matter. Co-existing iodine species (I - , IO 3 - , I 2 , and organoiodine compounds), in different proportions, has been reported in various terrestrial environments. However, there are conflicting reports regarding the environmental behavior of the different types of inorganic iodine and few publications on organic iodine compounds. This work examines the sorption and transport behavior of both inorganic and organic iodine species in geological samples from several complexes of the U.S. Department of Energy, where transport of radionuclides, including 129 I, may occur. Experiments on soils and sediments from the Savannah River Site in South Carolina, Oak Ridge Site in Tennessee, Hanford Site in Washington, Livermore Site 300 in California, and a surface soil from Santa Fe in New Mexico near Los Alamos were carried out. Samples from Savannah River Site and Livermore Site 300 are available from different depths. In addition, a surface soil of Wisconsin with a high amount of organic matter is utilized. This wide variety of sample types provides opportunities to examine the influence of

Immobilization of fission iodine by reaction with insoluble natural organic matter

International Nuclear Information System (INIS)

Steinberg, S.M.; Schmett, G.T.; Kimble, G.; Emerson, D.W.; Turner, M.F.; Rudin, M.

2008-01-01

Iodine-129 is a fission product and highly mobile in the environment. Along with other stable isotopes of iodine, 129 I is released during reprocessing of nuclear fuel and must be trapped to prevent the release of radioactivity to the environment. Past studies have provided evidence that iodine can become associated with natural organic matter (NOM). This research explores the use of NOM (sphagnum peat and humic acid) to sequester iodine from the vapor and aqueous phases. NOM-associated iodine may be stable for geological storage. NOM-sequestered iodine can be recovered by pyrolysis to prepare target materials for transmutation. The nature of the NOM-iodine association has been explored. (author)

Study on solubility and leaching property of Iodine-129 waste-forms for geological disposal. Document prepared by other institute, based on the trust contract

Energy Technology Data Exchange (ETDEWEB)

Sakashita, A.; Izumi, J. [Mitsubishi Heavy Industries, Ltd., Tokyo (Japan); Kitao, H. [Nuclear Development Corp., Tokai, Ibaraki (Japan); Ueta, S.; Okada, K.; Nakazawa, T.; Muroi, M. [Mitsubishi Materials Corp., Tokyo (Japan)

2002-02-01

As concern the study on the property of Iodine-129 waste-forms, the solubilities and leachabilities of iodine-sodalite and leachabilities of apatite containing Iodine were measured last year. The results in this year are summarized as follows. 1. Solubility and Leachability of Iodine-sodalite. Leachabilities and solubilities of the synthesized iodine-sodalite by HIP method were measured by means of a long-term leach test in the solution with chloride ions and high pH (12.5). The measured solubilities were within a range of 10{sup -3} - 10{sup -2} mol/L, which were larger compare with the previous values. The leachabilities were 10{sup -6} g/cm{sup 2}/day (powder) and 10{sup -3} g/cm{sup 2}/day (block). After the leach test, the solid phases were analyzed and the alternation was not observed. 2. Leaching Property of Apatite Sample which contains Iodine adsorption medicine. Apatite sample was manufactured from apatite and zeorait which adsorbs iodine matrix by plasma-hotpress. The porosity of the samples was under 5% and release rate of iodine was about 10% at plasma-hotpress manufacturing. The leachabilities of iodine were 10{sup -4} - 10{sup -3} g/cm{sup 2}/d at 56 day soaking period. These values were 1 - 2 digits higher compare with the leachabilities of calcium. It is thought that the iodine selectively is leached from apatite sample. (author)

Introduction to Test Facility for Iodine Retention in Filtered Containment Venting System

Energy Technology Data Exchange (ETDEWEB)

Jung, Jaehoon; An, Sang Mo; Ha, Kwang Soon; Kim, Hwan Yeol [KAERI, Daejeon (Korea, Republic of)

2015-05-15

In many countries the implementation of FCVS's is under discussion to mitigate fission product release not only in the short-term but also in the long-term view. To verify the performance of FCVS, the large-scaled tests have been performed such as advanced containment experiments (ACE), the iodine and aerosol retention rate test facility (JAVA), etc. The elemental and organic iodides are the main gaseous iodine species in the containment atmosphere. For the iodine retention, experimental programs have confirmed the existence of gaseous organic iodine in some cases in higher concentrations than for gaseous molecular iodine (I{sub 2}). The Reaction of Methyl iodide (CH{sub 3}I) with surfaces and the removal by containment filters and scrubbers is less efficient in comparison to molecular iodine. In the recent years, an experimental and analytical work has been conducted at the Paul Scherrer Institute (PSI) to develop a process leading to a fast, comprehensive and reliable retention of volatile iodine species in aqueous solutions. New FCVS test facility to verify the performance of FCVS is designed and under construction. The iodine retention tests are planned with elemental iodine or with organic iodide loaded carrier gas consisting of pure non-condensable gas, pure steam and of typical mixtures of non-condensable gas/steam. This paper introduces the iodine generation and measurement system for the iodine retention test of FCVS. In severe accidents elemental and organic iodides are the main gaseous iodine species in the containment atmosphere. Release of the gaseous species in sufficient quantities from containment to environment generates a risk for public health. The filtered containment venting systems (FCVS) can considerably reduce the leakage of radioactive materials to the environment. New integral test facility is prepared to verify a performance of the FCVS. The test facility consists of a test vessel, thermal-hydraulic, and aerosol/iodine generation and

Neutron activation and mass spectrometric measurement of /sup 129/I

International Nuclear Information System (INIS)

Strebin, R.S. Jr.; Brauer, F.P.; Kaye, J.H.; Rapids, M.S.; Stoffels, J.J.

1987-11-01

An integrated procedure has been developed for measurement of /sup 129/I by neutron activation analysis and mass spectrometry. An iodine isolation procedure previously used for neutron activation has been modified to provide separated iodine suitable for mass spectrometric measurement as well. Agreement between both methods has been achieved within error limits. The measurement limit by each method is about 10/sup 7/ atoms (2 fg) of /sup 129/I. 13 refs,. 4 figs., 1 tab

Importance of chemical speciation of iodine in relation to dose estimates from 129I

International Nuclear Information System (INIS)

Sheppard, S.C.

1996-12-01

Biota live in a chemical milieu and take up elements according to laws of chemistry and physics. Radioactivity is not important to accumulation processes. However, for radionuclides it is almost always the radiological consequences that are important. As such, most discussions and modelling of the processes of distribution, exposure and consequences tend to deal with radionuclides and do not dwell on chemistry. In fact, the chemical aspects of dose estimation are dealt with quite adequately, but usually in an implicit rather than explicit manner. This report discusses the chemistry and chemical speciation of iodine (1) and illustrates how these topics have been implicitly included in biosphere models such as BIOTRAC, the model employed in the assessment of Canada's nuclear fuel waste disposal concept. Iodine is emphasized because 129 I is the dominant contributor to the hypothetical doses estimated. Not all aspects of the behaviour of 1 are implicit in BIOTRAC, but the exceptions are of minor importance. In general, the very broad ranges in parameter values specified for BIOTRAC encompass substantial latitude for the possible effects of chemical behaviour and speciation. Nonetheless, detailed understanding of the behavior of 1 in the environment is essential to the credibility of models such as BIOTRAC. There is substantial room for improved knowledge of the speciation of I, especially in freshwater and soil environments. (author)

Environmental concentration and migration of 129I

International Nuclear Information System (INIS)

Brauer, F.P.; Strebin, R.S. Jr.

1982-01-01

Local sources of 129 I suitable for study of migration in the environment are uranium ore bodies for long periods and nuclear fuel reprocessing operations for recent periods. Uranium ores produce 129 I from spontaneous and neutron-induced fission. Nuclear fuel reprocessing has resulted in releases of 129 I to both the atmosphere and the hydrosphere. The long-term fate of surface-deposited and groundwater 129 I was studied. Neutron activation analysis was used to measure the low levels of 129 I and natural 127 I in samples near and remote from nuclear fuel reprocessing facilities. Measurements were made on air samples, vegetation, soil, surface water, groundwater and uranium ore samples. Samples were collected both during reprocessing operations and after reprocessing activities had been discontinued for several years. The 129 I was found to accumulate in the top soil and litter layer. The surface concentrations of 129 I in forest communities were found to be several times higher than for nearby grass communities. The 129 I levels were found to persist in the environment after reprocessing activities had been discontinued. Measurable 129 I was found to be contained in uranium ore samples from a variety of locations and with a range of uranium concentrations. Thus ore bodies constitute a source of 129 I suitable for study of migration over long periods. Iodine-129 has entered surface and groundwater as the result of liquid and atmospheric discharges from nuclear fuel reprocessing facilities. The iodine in water samples was found to be anionic and travel with the water flow. Thus 129 I was found to provide high sensitivity for hydrology tracer studies and radioactivity migration surveillance. Once 129 I enters the hydrosphere it migrates with the water with little or no hold-up by exchange with cationic exchangers such as soil or silt

Identification of Promising Remediation Technologies for Iodine in the UP-1 Operable Unit

Energy Technology Data Exchange (ETDEWEB)

Strickland, Christopher E. [Pacific Northwest National Lab. (PNNL), Richland, WA (United States); Johnson, Christian D. [Pacific Northwest National Lab. (PNNL), Richland, WA (United States); Lee, Brady D. [Pacific Northwest National Lab. (PNNL), Richland, WA (United States); Qafoku, Nikolla [Pacific Northwest National Lab. (PNNL), Richland, WA (United States); Szecsody, James E. [Pacific Northwest National Lab. (PNNL), Richland, WA (United States); Truex, Michael J. [Pacific Northwest National Lab. (PNNL), Richland, WA (United States); Vermeul, Vincent R. [Pacific Northwest National Lab. (PNNL), Richland, WA (United States)

2017-09-01

Iodine-129 (129I) generated at the U.S. Department of Energy (DOE) Hanford Site during plutonium production was released to the subsurface, resulting in several large, though dilute, plumes in the groundwater, including the plume in the 200-UP-1 operable unit (OU). Because 129I is an uncommon contaminant, relevant remediation experience and scientific literature are limited, though work is under way to better understand the fate and transport of 129I in the environment and the effectiveness of potential remediation technologies. The recent UP-1 Evaluation Plan for Iodine and report on the Conceptual Model of Iodine Behavior in the Subsurface at the Hanford Site provide information on the history of contamination in the 200-UP-1 OU, relevant controlling processes (biological and geochemical), risk, the conceptual site model, and potential remedial options, which provided a foundation for this study. In this study, available information was compiled and used to categorize potential remediation technologies, culminating in a recommendation of promising technologies for further evaluation. Approaches to improve the technical information about promising technologies are also recommended in this study so that a subsequent evaluation of potential remediation alternatives can assess these technologies.

Speciation of iodine (I-127) in the natural environment around Canadian CANDU sites

International Nuclear Information System (INIS)

Kramer, S.J.; Kotzer, T.G.; Chant, L.A.

2001-06-01

In Canada, very little data is available regarding the concentrations and chemical speciation of iodine in the environment proximal and distal to CANDU Nuclear Power Generating Stations (NPGS). In the immediate vicinity of CANDU reactors, the short-lived iodine isotope 131 I (t 1/2 = 8.04 d), which is produced from fission reactions, is generally below detection and yields little information about the environmental cycling of iodine. Conversely, the fission product 129 I has a long half-life (t 1/2 = 1.57x10 7 y) and has had other anthropogenic inputs (weapons testing, nuclear fuel reprocessing) other than CANDU over the past 50 years. As a result, the concentrations of stable iodine ( 127 I) have been used as a proxy. In this study, a sampling system was developed and tested at AECL's Chalk River Laboratories (CRL) to collect and measure the particulate and gaseous inorganic and organic fractions of stable iodine ( 127 I) in air and associated organic and inorganic reservoirs. Air, vegetation and soil samples were collected at CRL, and at Canadian CANDU Nuclear Power Generating Stations (NPGS) at OPG's (Ontario Power Generation) Pickering (PNGS) and Darlington NPGS (DNGS) in Ontario, as well as at NB Power's Pt. Lepreau NPGS in New Brunswick. The concentrations of particulate and inorganic iodine in air at CRL were extremely low, and were often found to be below detection. The concentrations are believed to be at this level because the sediments in the CRL area are glacial fluvial and devoid of marine ionic species, and the local atmospheric conditions at the sampling site are very humid. Concentrations of a gaseous organic species were comparable to worldwide levels. The concentrations of particulate and inorganic iodine in air were also found to be low at PNGS and DNGS, which may be attributed to reservoir effects of the large freshwater lakes in southern Ontario, which might serve to dilute the atmospheric iodine concentrations. The concentrations of

Some methods of detection of atmospheric contamination by iodine 131

International Nuclear Information System (INIS)

Billard, Francois; Chevalier, Gerard; Gaillard, Pierre; Pradel, Jacques

1964-01-01

Due to the extensive use of iodine, risks of contamination by iodine 131 are increasing. Moreover, the increase of reactor power requires venting installations equipped with efficient safety filters which must be tested. The authors thus report the study of iodine trapping in filters, and its atmospheric detection and measurement. They report studies and achievements in the field of measurement of atmospheric pollution, and tests performed on iodine trapping by activated coals. After having outlined key qualities of an apparatus for atmospheric control, the authors indicate the various sampling methods. They discuss the method and calibration for the measurement of radioactivity of filters and coal which have trapped iodine 131. They discuss measurement sensitivity. They report how the efficiency of coals has been checked. They describe the experimental installation, and report the tests of some detectors of atmospheric contamination: sampling cartridges full of activated coal, gas mask cartridge, continuous control apparatus ('coffee machine' type), and detector of gaseous iodine. Appendices indicate the calculation of error on a cartridge counting rate, iodine generation methods (discontinuous method, continuous method) [fr

Determination method for 129I in soil samples by MIP-MS

International Nuclear Information System (INIS)

Uezu, Yasuhiro; Nakano, Masanao; Fujita, Hiroki; Watanabe, Hitoshi; Maruo, Yoshihiro

2001-01-01

The radioactive iodine-129 ( 129 I) is an important radionuclide for environmental assessment because it has a long half-life and is accumulated in the thyroid gland in humans. A new analytical technique by Microwave Induced Plasma Mass Spectrometer (MIP-MS) was applied to the determination of 129 I in soil samples. In environmental samples, a large amount of matrix elements are present. Therefore, the matrix elements were eliminated by ashing at 1000degC, and iodine isotopes were trapped by an activated charcoal and finally extracted by 10% tetramethylammonium hydroxide (TMAH). The concentration of 129 I in a soil samples were compared between results of neutron activation analysis and MIP-MS method. The results showed an excellent agreement. (author)

Iodine isotopes species fingerprinting environmental conditions in surface water along the northeastern Atlantic Ocean

DEFF Research Database (Denmark)

He, Peng; Hou, Xiaolin; Aldahan, Ala

2013-01-01

Concentrations and species of iodine isotopes (127I and 129I) provide vital information about iodine geochemistry, environmental conditions and water masses exchange in oceans. Despite extensive investigations of anthropogenic 129I in the Arctic Ocean and the Nordic Seas, concentrations of the is...... 129I in ocean environments and impact on climate at the ocean boundary layer.......Concentrations and species of iodine isotopes (127I and 129I) provide vital information about iodine geochemistry, environmental conditions and water masses exchange in oceans. Despite extensive investigations of anthropogenic 129I in the Arctic Ocean and the Nordic Seas, concentrations...... of the isotope in the Atlantic Ocean are, however, still unknown. We here present first data on 129I and 127I, and their species (iodide and iodate) in surface water transect along the northeastern Atlantic between 30° and 50°N. The results show iodate as the predominant species in the analyzed marine waters...

Theoretical study of the thermochemical properties of gaseous iodine compounds: incidences in atmospheric chemistry and nuclear safety

International Nuclear Information System (INIS)

Louis, F.; Fortin, C.; Cornet, M.; Khanniche, S.; Skoviera, J.; Cantrel, L.; Cernusak, I.

2015-07-01

Thermochemical properties (ΔfH 0 298K , S 0 298K et C p = f(T)) have been determined for a series of gaseous iodine-containing compounds by using quantum chemistry tools. Different levels of theory have been employed in this work in order to predict geometrical parameters and the energetics including spin-orbit coupling. The use of the B3LYP functional for the geometry optimization followed by a calculation of the total electronic energies using the Dual Level method allows to her standard enthalpies of formation at 298 K in good agreement with the available literature data. (authors)

Radioactive iodine absorbing properties of tetrathiafulvalene

Energy Technology Data Exchange (ETDEWEB)

Ito, Tomiyasu; Nakamura, Asao (Ajinomoto Co. Inc., Kawasaki, Kanagawa (Japan). Central Research Labs.); Nogawa, Norio; Oohashi, Kunio; Morikawa, Naotake

1989-05-01

For the purpose of searching some effective absorbents of gaseous radioactive iodine, 16 substances considered as having an affinity for iodine were investigated with regular iodine and /sup 125/I. In a preliminary survey, only tetrathiafulvalene (TTF) was found to have satisfactory absorbing properties comparable to activated charcoal. A further detailed comparison of the properties between TTF and activated charcoal led us to the conclusion that the former has more preferable properties as absorbent of radioactive iodine than the latter in all points studied. The results are summarized as follows: (1) The absorption of iodine on TTF in atmosphere was about twice as much as that on activated charcoal. Desorption of iodine from saturatedly absorbed iodine on TTF was practically negligible except trace amount of initial desorption, while that on activated charcoal was considerable (3%/50h) even in the air at room temperature. (2) Absorbed amount of iodine on activated charcoal decreased with increasing gaseous iodine concentration, air flow rate, on humidity of flowing-air. On the other hand, those factors scarcely affected that on TTF. Under an air flow rate of 1m/s, activated charcoal absorbs only 80% of iodine, while TTF absorbs more than 99%. (3) In flowing-air saturated with water vapor, iodine absorbed on activated charcoal was gradually liberated although by small amount (0.08%/100h), while that on TTF was much more stable for a long period (0.004%/100h). As a conclusion, TTF is considered to be useful as a quite effective radioactive iodine absorbent, especially in the case where protection from radioactive iodine should be serious, though it is expensive now. (author).

Radioactive iodine absorbing properties of tetrathiafulvalene

International Nuclear Information System (INIS)

Ito, Tomiyasu; Nakamura, Asao; Nogawa, Norio; Oohashi, Kunio; Morikawa, Naotake.

1989-01-01

For the purpose of searching some effective absorbents of gaseous radioactive iodine, 16 substances considered as having an affinity for iodine were investigated with regular iodine and 125 I. In a preliminary survey, only tetrathiafulvalene (TTF) was found to have satisfactory absorbing properties comparable to activated charcoal. A further detailed comparison of the properties between TTF and activated charcoal led us to the conclusion that the former has more preferable properties as absorbent of radioactive iodine than the latter in all points studied. The results are summarized as follows: (1) The absorption of iodine on TTF in atmosphere was about twice as much as that on activated charcoal. Desorption of iodine from saturatedly absorbed iodine on TTF was practically negligible except trace amount of initial desorption, while that on activated charcoal was considerable (3%/50h) even in the air at room temperature. (2) Absorbed amount of iodine on activated charcoal decreased with increasing gaseous iodine concentration, air flow rate, on humidity of flowing-air. On the other hand, those factors scarcely affected that on TTF. Under an air flow rate of 1m/s, activated charcoal absorbs only 80% of iodine, while TTF absorbs more than 99%. (3) In flowing-air saturated with water vapor, iodine absorbed on activated charcoal was gradually liberated although by small amount (0.08%/100h), while that on TTF was much more stable for a long period (0.004%/100h). As a conclusion, TTF is considered to be useful as a quite effective radioactive iodine absorbent, especially in the case where protection from radioactive iodine should be serious, though it is expensive now. (author)

Iodine-129 in human thyroids and seaweed in China

DEFF Research Database (Denmark)

Hou, Xiaolin; Dahlgaard, H.; Nielsen, S.P.

2000-01-01

The concentrations of I-129 and the ratios of I-129/I-127 in normal human thyroids collected in Tianjin, China, and some seaweed samples from the Chinese coast were determined by neutron activation analysis. The mean I-129/I-127 ratio in these thyroids was found to be 1.13 x 10(-9), which is two...... orders of magnitude higher than the level of the pre-nuclear era, but one order of magnitude lower than the level in Europe in the post-nuclear era. There is no significant difference between the ratio of I-129/I-127 in the thyroids for the post-nuclear era from China and other areas, which...

Behaviour of radioiodine in gaseous effluents

International Nuclear Information System (INIS)

Barry, P.J.

1968-01-01

Because of the different chemical forms in which radioiodine occurs in the gaseous state, it is important when designing efficient filters to know the chemical forms which may be present in the effluent gases when various operations are being carried out and to know the effect of different gaseous environments on the filtration efficiency. To obtain this information it is necessary to have available reliable means of characterizing different chemical forms and to sample gaseous effluents when these operations are being carried out. This paper describes the use for identifying molecular iodine of metallic screens in a multi-component sampling pack in different gaseous environments. Using multi-component sampling packs, the fractionation of iodine nuclides between different chemical forms was measured in the effluent gases escaping from an in-pile test loop in which the fuel was deliberately ruptured by restricting the flow of coolant. Sequential samples were taken for six hours after the rupture and it was possible to follow during this period the individual behaviours of 13 '1I, 133 I and 135 I. Simultaneous samples were also obtained of the noble gases in the effluent gas stream and of the iodine nuclides in the loop coolant. Similar experiments have been carried out with a view to characterizing the different chemical behaviour of radioiodine as it is released from a variety of operations in the nuclear industry including the cutting of fuel sections in metallurgical examination caves and an incinerator. (author)

Iodine binding to humic acid.

Science.gov (United States)

Bowley, H E; Young, S D; Ander, E L; Crout, N M J; Watts, M J; Bailey, E H

2016-08-01

The rate of reactions between humic acid (HA) and iodide (I(-)) and iodate (IO3(-)) have been investigated in suspensions spiked with (129)I at concentrations of 22, 44 and 88 μg L(-1) and stored at 10 °C. Changes in the speciation of (129)I(-), (129)IO3(-) and mixed ((129)I(-) + (129)IO3(-)) spikes were monitored over 77 days using liquid chromatography inductively coupled plasma mass spectrometry (LC-ICP-MS). In suspensions spiked with (129)I(-) 25% of the added I(-) was transformed into organic iodine (Org-(129)I) within 77 days and there was no evidence of (129)IO3(-) formation. By contrast, rapid loss of (129)IO3(-) and increase in both (129)I(-) and Org-(129)I was observed in (129)IO3(-)-spiked suspensions. However, the rate of Org-(129)I production was greater in mixed systems compared to (129)IO3(-)-spiked suspensions with the same total (129)I concentration, possibly indicating IO3(-)I(-) redox coupling. Size exclusion chromatography (SEC) demonstrated that Org-(129)I was present in both high and low molecular weight fractions of the HA although a slight preference to bond with the lower molecular weight fractions was observed indicating that, after 77 days, the spiked isotope had not fully mixed with the native (127)I pool. Iodine transformations were modelled using first order rate equations and fitted rate coefficients determined. However, extrapolation of the model to 250 days indicated that a pseudo-steady state would be attained after ∼200 days but that the proportion of (129)I incorporated into HA was less than that of (127)I indicating the presence of a recalcitrant pool of (127)I that was unavailable for isotopic mixing. Copyright © 2016 Elsevier Ltd. All rights reserved.

Phebus FPT-O. Exploratory containment iodine chemistry calculations

International Nuclear Information System (INIS)

Fermandjian, J.; Dickinson, S.; Edward, J.B.; Ewig, F.J.; Funke, F.; Hueber, C.; Rodriguez-Maroto, J.J.; Sims, H.E.

1994-01-01

The results of the exploratory containment iodine chemistry calculations related to the first Phebus-FP test (benchmark exercise for explaining the reasons for code inconsistencies and realistic calculation for test preparation) are reported. Calculations have been performed by CEA/IPSN/DRS/SEMAR-Cadarache (France), CIEMAT-Madrid (Spain), GRS-Koeln and SIEMENS/KWU, Erlangen (Germany), AEA-Harwell (UK), Ontario Hydro-Toronto, University of Toronto and AECL-Whiteshell (Canada). The code benchmark results show that mechanistic codes (INSPECT and LIRIC) are in agreement for molecular iodine concentration in the gaseous phase, whereas empirical codes (IODE and IMPAIR) are in disagreement because they model differently HOI disproportionation and use different radiolytic constant values (iodide/iodate radiolysis). Furthermore, the molecular iodine concentrations in the gaseous phase are 10 to 100 times higher at acid pH (pH - 5) than at neutral pH (pH - 7), and the presence of organic radicals in water does not change the concentrations of inorganic iodine species. Concerning the realistic calculation, the iodine mass distribution in the containment differ from one code to another, but all codes predict that the iodine concentration in the gaseous phase is high enough to be detected by foreseen instrumentation (as was verified during the test). FPT-0 test has been performed in December 1993. Analysis of experimental results is underway and result interpretation will be available at the beginning of 1995. (author). 11 refs., 1 tab., 5 figs

Geochemical Cycling of Iodine Species in Soils

International Nuclear Information System (INIS)

Hu, Q.; Moran, J.E.; Blackwood, V.

2007-01-01

Iodine is an important element in studies of environmental protection and human health, global-scale hydrologic processes and nuclear nonproliferation. Biogeochemical cycling of iodine in soils is complex, because iodine occurs in multiple oxidation states and as inorganic and organic species that may be hydrophilic, atmophilic, and biophilic. In this study, we applied new analytical techniques to study the content and speciation of stable iodine in representative surface soils, and sorption and transport behavior of iodine species (iodide, iodate, and 4-iodoaniline) in sediments collected at numerous nuclear facilities in the United States, where anthropogenic 129 I from prior nuclear fuel processing activities poses an environmental risk. The surface soil samples were chosen for their geographic locations (e.g., near the ocean or nuclear facilities) and for their differing physico-chemical characteristics (organic matter, texture, etc). Extracted solutions were analyzed by IC and ICP-MS methods to determine iodine concentrations and to examine iodine speciation (iodide, iodate, and organic iodine). In natural soils, iodine is mostly (nearly 90% of total iodine) present as organic species, while inorganic iodine becomes important (up to 50%) only in sediments with low organic matter. Results from laboratory column studies, aimed at examining transport of different iodine species, showed much greater retardation of 4-iodoaniline than iodide or iodate. Careful attention must be given to potential interconversion among species when interpreting the biogeochemical behavior of iodine in the environment. In addition to speciation, input concentration and residence time effects will influence the biogeochemical cycling of anthropogenic 129I deposited on surface soils

Speciation of iodine (I-127) in the natural environment around Canadian CANDU sites

Energy Technology Data Exchange (ETDEWEB)

Kramer, S.J.; Kotzer, T.G.; Chant, L.A

2001-06-01

In Canada, very little data is available regarding the concentrations and chemical speciation of iodine in the environment proximal and distal to CANDU Nuclear Power Generating Stations (NPGS). In the immediate vicinity of CANDU reactors, the short-lived iodine isotope {sup 131}I (t{sub 1/2} = 8.04 d), which is produced from fission reactions, is generally below detection and yields little information about the environmental cycling of iodine. Conversely, the fission product {sup 129}I has a long half-life (t{sub 1/2} = 1.57x10{sup 7} y) and has had other anthropogenic inputs (weapons testing, nuclear fuel reprocessing) other than CANDU over the past 50 years. As a result, the concentrations of stable iodine ({sup 127}I) have been used as a proxy. In this study, a sampling system was developed and tested at AECL's Chalk River Laboratories (CRL) to collect and measure the particulate and gaseous inorganic and organic fractions of stable iodine ({sup 127}I) in air and associated organic and inorganic reservoirs. Air, vegetation and soil samples were collected at CRL, and at Canadian CANDU Nuclear Power Generating Stations (NPGS) at OPG's (Ontario Power Generation) Pickering (PNGS) and Darlington NPGS (DNGS) in Ontario, as well as at NB Power's Pt. Lepreau NPGS in New Brunswick. The concentrations of particulate and inorganic iodine in air at CRL were extremely low, and were often found to be below detection. The concentrations are believed to be at this level because the sediments in the CRL area are glacial fluvial and devoid of marine ionic species, and the local atmospheric conditions at the sampling site are very humid. Concentrations of a gaseous organic species were comparable to worldwide levels. The concentrations of particulate and inorganic iodine in air were also found to be low at PNGS and DNGS, which may be attributed to reservoir effects of the large freshwater lakes in southern Ontario, which might serve to dilute the atmospheric iodine

129I in volcanic fluids: Testing for the presence of marine sediments in the Central American volcanic arc

International Nuclear Information System (INIS)

Snyder, Glen; Fehn, Udo

2000-01-01

The long half-life and the geochemical behavior of the 129 I system suggest that this cosmogenic radioisotope can contribute significantly to the understanding of processes associated with subduction zones and volcanic arc systems. Because iodine is not incorporated into igneous rocks, the age-signal associated with 129 I permits the determination of the origin of volatiles within arc volcanic systems. We report here results of a study to test the application of 129 I in fluids collected from hotsprings, crater lakes, fumaroles and geothermal wells from the Central American volcanic arc. Both the Momotombo geothermal field in Nicaragua and the Miravalles geothermal field in Costa Rica show 129 I/I ratios consistent with magmatic contributions from subducted marine pelagic sediments (minimum iodine ages of 25-30 Ma). In addition, several wells provide iodine isotopic ratios indicative of an older end-member, presumably located in the shallow crust (minimum iodine age = 65 Ma)

Conceptual Model of Iodine Behavior in the Subsurface at the Hanford Site

Energy Technology Data Exchange (ETDEWEB)

Truex, Michael J. [Pacific Northwest National Lab. (PNNL), Richland, WA (United States); Lee, Brady D. [Pacific Northwest National Lab. (PNNL), Richland, WA (United States); Johnson, Christian D. [Pacific Northwest National Lab. (PNNL), Richland, WA (United States); Qafoku, Nikolla P. [Pacific Northwest National Lab. (PNNL), Richland, WA (United States); Last, George V. [Pacific Northwest National Lab. (PNNL), Richland, WA (United States); Lee, Michelle H. [Pacific Northwest National Lab. (PNNL), Richland, WA (United States); Kaplan, Daniel I. [Pacific Northwest National Lab. (PNNL), Richland, WA (United States)

2015-09-01

The fate and transport of 129I in the environment and potential remediation technologies are currently being studied as part of environmental remediation activities at the Hanford Site. A conceptual model describing the nature and extent of subsurface contamination, factors that control plume behavior, and factors relevant to potential remediation processes is needed to support environmental remedy decisions. Because 129I is an uncommon contaminant, relevant remediation experience and scientific literature are limited. Thus, the conceptual model also needs to both describe known contaminant and biogeochemical process information and to identify aspects about which additional information needed to effectively support remedy decisions. this document summarizes the conceptual model of iodine behavior relevant to iodine in the subsurface environment at the Hanford site.

Iodine-129 in aquatic organisms near nuclear fuels processing plants

International Nuclear Information System (INIS)

Watson, D.G.

1975-04-01

Concentrations of 129 I in two aquatic habitats near nuclear fuel processing plants were highest in algae and crustaceans. These two forms may be useful in future monitoring of 129 I. There is some indication of an increase in atom ratios and specific activity in aquatic organisms over that in water and sediments. Additional measurements should be made to verify this conclusion. Efforts should continue to measure the possible long term build-up of 129 I in aquatic environments receiving effluents from fuels reprocessing plants. Even at very low rates of release to the environment, the long physical half-life of 129 I creates the potential for build-up of this nuclide to significant levels. (U.S.)

The retention of iodine by iodine filters in nuclear power plants in the case of fire

International Nuclear Information System (INIS)

Giraud, V.

1985-01-01

Due to the liberation of considerable amounts of gaseous combustion products, fires in nuclear power plants may lead to a deterioration in the retention of radioiodine by iodine filters. The combustion products of the burnable materials, i.e., insulations, lubricants and paints, vary considerably with the development of the fire. Combustion product analyses of these materials have been performed only to a limited extent. The reaction of iodine with combustion products as well as the retention of the resulting iodine reaction products by sorbents have not yet been investigated. The reduction in the removal efficiencies of iodine sorbents due to the presence of combustion products is unknown. (orig.) [de

Aged anthropogenic iodine in a boreal peat bog

International Nuclear Information System (INIS)

Maillant, S.; Sheppard, M.I.; Denys, S.; Leclerc Cessac, E.

2004-01-01

Iodine-129 is a radionuclide of major concern in the international safety assessments for deep geological storage and disposal of nuclear waste because it migrates quickly through the geosphere to the biosphere and then from the soil to humans through the food-chain. However, in organic soils the 129 I may be immobilized over a long time period, and so these soils represent a potential accumulation point in the biosphere. Effects of long residence times of iodine in soils are scarce. The present paper gives some insight on the aging of stable iodine, under natural conditions. Stable iodine was introduced as KI in 1987 at the base of a small natural sphagnum bog to simulate arrival of iodine via a groundwater discharge from the geosphere. Previous data revealed the spread of the iodine outwards spatially from the basal spike and also recorded its rise towards the bog surface. Fifteen years later, the groundwater, the soil and the vegetation have been sampled and analyzed for iodine. The results we will present give insight on the mobility of 'aged' iodine with time, the retention properties of the peat, and provide iodine transfer factors for native boreal plant species. The data show iodine: - continues to slowly spread from the spike after 15 years, - is more strongly retained on the solid phase at the surface than at depth, - the chemical structure of the peat may influence the retention of iodine as shown by NMR analysis, - iodine retention has become greater with time, and - herbaceous species are the greatest accumulators. This study demonstrates bogs present good sinks for iodine and limit the transfer of iodine to some of the 'wildlife' food-chains. (author)

Iodine and microbial interactions in an organic soil

International Nuclear Information System (INIS)

Sheppard, M.I.; Hawkins, J.L.

1995-01-01

Iodine-129 in groundwater discharging from a geological disposal vault could accumulate in wetlands by chemical sorption onto low pH, highly organic solid surfaces or by direct or indirect microbial processes. Previous work indicated that saturation of anion sorption sites, microbial toxicity, or swamping of the I reduction/oxidation reaction decreased the retention of a wetland sphagnum for iodine with increased iodine porewater concentrations. Bog water and peat of an iodine-rich bog were studied to elucidate the role of micro-organisms in the retention and accumulation of iodine in a temperate wetland. (author)

Transmutation of 129I Using an Accelerator-Driven System

International Nuclear Information System (INIS)

Nishihara, Kenji; Takano, Hideki

2002-01-01

A conceptual blanket design for 129 I transmutation is proposed for an accelerator-driven system (ADS) that is designed to transmute minor actinides (MAs). In this ADS, 250 kg/yr of MA and 56 kg/yr of iodine are simultaneously transmuted, and they correspond to the quantities generated from ∼10 units of existing light water reactors. Furthermore, an introduction scenario and the benefit of iodine transmutation are studied for future introduction of fast breeder reactors. It is shown that the transmutation of iodine benefits the concept of underground disposal

Brain Imaging Using Hyperpolarized 129Xe Magnetic Resonance Imaging.

Science.gov (United States)

Chahal, Simrun; Prete, Braedan R J; Wade, Alanna; Hane, Francis T; Albert, Mitchell S

2018-01-01

Hyperpolarized (HP) 129 Xe magnetic resonance imaging (MRI) is a novel iteration of traditional MRI that relies on detecting the spins of 1 H. Since 129 Xe is a gaseous signal source, it can be used for lung imaging. Additionally, 129 Xe dissolves in the blood stream and can therefore be detectable in the brain parenchyma and vasculature. In this work, we provide detailed information on the protocols that we have developed to image 129 Xe within the brains of both rodents and human subjects. © 2018 Elsevier Inc. All rights reserved.

Determination of chemical form of iodine with IC-ICP-MS system and its application to the environmental samples

International Nuclear Information System (INIS)

Yoshida, S.; Katou, S.; Sekimoto, H.; Muramatsu, Y.

2005-01-01

Iodine-129 is one of the important radionuclides possibly released into the environment from nuclear weapons testing and from the nuclear facilities such as nuclear fuel reprocessing plants. Because of its long half-life (1.57 x 10 7 y), knowing its long-term behavior in the environment is a major concern. As I-129 is expected to act together with stable iodine (I-127) in the environment after long time, the biogeochemical cycling of stable iodine in the environment can be used for the reliable safety assessment of I-129. Chemical form is the one of the important factors controlling the 'iodine behavior in the environment. Iodide (I - ) and iodate (IO 3 - ) are known to be the major chemical form in the aqueous solution. However, the information on the chemical form of iodine in the environmental sample is limited because of lack of reliable analytical technique for trace level of iodine in the environment. In this study, the analytical system by using ion chromatograph (IC) followed by inductively coupled plasma mass spectrometry (ICP-MS) was developed for the separate determination of I - and IO 3 - in the aqueous solution. The IC with anion exchange column (EXCELPAK ICS-A23) was used for the separation of I - and IO 3 - with 30 mM (NH 4 ) 2 CO 3 as eluent. Separated iodine was determined with ICP-MS on line. with the detection limit 0.1 - 1 μg/L. The total iodine concentration was also measured by the direct determination with ICP-MS. The iodine in the several environmental samples such as irrigation water in paddy field was successfully determined with information of chemical form. In incubation experiment with flooded soil, the change of the chemical form of iodine in the soil solution with change of Eh was observed. Detailed data will be discussed in the presentation.

Neutron activation analysis of 127I and 129I environmental samples

International Nuclear Information System (INIS)

Takeishi, Minoru; Namiki, Atsushi; Ishida, Junichiro; Iwai, Makoto

1987-01-01

The analytical method of 127 I and 129 I in environmental samples has been studied and the background levels of these nuclides in soils, seaweeds and milk were measured. The analytical method consists of the combustion technique and neutron activation analysis (N.A.A.). The iodine was separated from samples by ignition at about 1,000 deg C in a quartz combustion apparatus with an oxygen and a nitrogen stream, and was absorbed by small amounts of active charcoal. The iodine was then purified through the carbontetrachloride extraction method and the PdI 2 decomposition method. Irradiation was conducted by JRR-4 (n th : 8 x 10 13 n/cm 2 · sec) for 40 min. After irradiation, the iodine was purified by the solvent extraction method same as pre-irradiation extraction. Each activity of 126 I and 130 I, which was produced by 127 I(n,2n) 126 I and 129 I(n,γ) 130 I reaction respectively, was measured by γ-spectrometry using a Ge-detector. The lower detection limits of 129 I by this method were 4 x 10 -7 Bq/g for dry soil, 7 x 10 -8 Bq/g for fresh seaweeds and 7 x 10 -6 Bq/l for fresh milk, respectively. The relative standard deviation of 129 I measurements in soil and milk were less than 10 %. (author)

Kinetic cartography of radioisotopes of iodine in the thyroid follicles of the new-born rats under low or standard iodine diet: Analyzed using Secondary Ion Mass Spectrometry (NanoSIMS50): Contribution to the study of the consequences of Chernobyl

International Nuclear Information System (INIS)

Elbast, M.

2008-03-01

The most significant impact of the Chernobylsk accident is the increased incidence of thyroid cancers among children in contaminated areas. To estimate the radiation dose provided by radioiodine released after Chernobylsk (iodine 131 and short-lived isotopes, iodine 132, 133, 134, 135), we used new-born rats to mimic the situation of fallout contamination (young age and iodine deficiency). The pups, under low iodine diet and under standard diet, were contaminated with 129 I at ages varying between 2 to 15 days and sacrificed 1, 4, 8, 24 hours and 4, 8 days after contamination. The variation in intra colloidal iodine distribution from 1 hour to 8 days was performed using a new ionic nano probe (NanoSIMS50). This method permits to discriminate between the newly incorporated iodine (129) and the initial pool of iodine (127). SIMS observations permit to heterogeneous intra and inter follicular distribution of 129 I. Iodine deficiency increases the absorbed amounts of iodine by a factor 10. Dosimetric estimations show an important contribution of short-lived radioiodine to the total thyrocyte dose. In conclusion, we have demonstrated that the age and the iodine deficiency accelerate the absorption of iodine in follicles and that the contribution of short-lived iodine connate ne neglected. (author)

Mitigation of release of volatile iodine species during severe reactor accidents - a novel reliable process of safety technology

International Nuclear Information System (INIS)

Guentay, S.; Bruchertseifer, H.

2010-01-01

In severe accidents, a significant risk for public health may be generated as a result of release of the gaseous iodine species into the environment through the containment leaks or containment venting filter systems with low retention efficiency. The elemental iodine and volatile organic iodides are the main gaseous iodine species in the containment. Potential release of large quantities of gaseous elemental iodine from the reactor coolant system or its radiolytic generation in the containment sump constitute the key source of gaseous elemental iodine in containment atmosphere. Iodine paint reactions as well as the reaction of iodine with organic residuals in sump water are the main mechanisms for the generation of high volatile organic iodides in the containment. Although very much desired, significant research activities conducted in 70's unfortunately did not create any technically feasible solution to mitigate iodine release into the environment under prevailing conditions. Development of a process leading to a fast, comprehensive and reliable retention of volatile iodine species in aqueous solution with an aim to implement for the severe accident management applications has been subject of a research project in the recent years at Paul Scherrer Institut. The process developed utilizes simultaneous use of two customary technical chemical additives in an aqueous solution. The results of the experimental program have demonstrated a fast and reliable destruction of high volatile organic iodine species and fast reduction of elemental iodine into iodide ions in aqueous solutions and an efficient mitigation of the re-formation of gaseous iodine from iodide ions. Investigations covered a broad range of anticipated severe accident conditions in the containment. The project additionally focused on possible application of the process to existing containment venting filter systems, specifically as a passive add-on for back-fitting. This paper describes the process

Simulation of ISTP-EPICUR Iodine Chemistry Tests with RAIM

Energy Technology Data Exchange (ETDEWEB)

Kim, Han-Chul; Cho, Yeong-Hun; Jang, Dong-Ju; Ryu, Myung-Hyun [Nuclear Korea Institute of Nuclear Safety, Daejeon (Korea, Republic of)

2014-10-15

The amount of iodine release largely depends on its volatility in the containment. Iodine has several chemical forms including aerosols, vapor, and gas. Among them gaseous iodine such as I{sub 2} and organic iodide are dominating due to their high volatility. Therefore, such iodine behavior has been extensively examined. Korea Institute of Nuclear Safety (KINS) has been joining the relevant international programs such as ISTP-EPICUR, OECD-BIP and OECD-STEM. In the course of this study, a simple iodine model, RAIM (Radio-Active Iodine chemistry Model) has been developed, based on the IMOD methodology and other previous studies. This model deals with chemical reactions associated with formation and destruction of iodine species in the containment atmosphere and the sump in a simple manner, as shown in Fig. 1. It also treats adsorption and desorption of volatile iodine on the paint surface. The iodine species modeled are inorganic volatile iodine, organic iodides of high volatility (HVRI) and low volatility (LVRI), non-volatiles, non-aqueous iodine, and iodine oxide aerosols (IO{sub x}). Many other material participating in the iodine reactions, e.g., air radiolysis products (ARP) such as ozone, are also modeled. This paper especially shows the analysis results after addition of gaseous reaction model to RAIM, which was further accompanied by adjustments of the existing reaction rate constants even for the aqueous reactions. After integration of iodine reaction models for gas and aqueous phase, RAIM was applied the S1-9 and S1-11 tests which were carried out in aqueous phase. In addition, re-analysis of the S2-6-5-2 test, for which iodine-loaded coupons were tested in gas phase, was also performed.

Separation and retention of iodine

International Nuclear Information System (INIS)

Thomas, T.R.

1976-01-01

Caustic and mercuric nitrate scrubbers have been used for iodine recovery from process offgas, but they exhibit low decontamination factors for organic iodide removal and produce liquid wastes that are unsuitable for final storage. The Iodox process gives high decontamination factors for both organic iodides and elemental iodine. The liquid waste can be evaporated to a solid or concentrated and fixed in cement. Efficient separation and retention of gaseous iodine species can be obtained with silver-loaded adsorbents. The waste is a dry solid easily handled and stored. Adsorbents containing cheaper metals appear to have lower iodine-loading capacities and may be unsuitable for bulk iodine removal from process offgas because of the large amounts of solid waste that would be generated. A potential method for regenerationg and recycling silver-loaded adsorbents is being evaluated. In conjunction with the regeneration, lead-exchanged zeolite is used as a secondary adsorbent for the final fixation and storage of the iodine

Chemical thermodynamics of iodine species in the HTGR fuel particle

International Nuclear Information System (INIS)

Lindemer, T.B.

1982-09-01

The iodine-containing species in an intact fuel particle in the high-temperature gas-cooled reactor (HTGR) have been calculated. Assumptions include: (1) attainment of chemical thermodynamic equilibrium among all species in the open porosity of the particle, primarily in the buffer layer; and (2) fission-product concentrations in proportion to their yields. The primary gaseous species is calculated to be cesium iodide; in carbide-containing fuels, gaseous barium iodide may exhibit equivalent pressures. The condensed iodine-containing phase is usually cesium iodide, but in carbide-containing fuels, barium iodide may be stable instead. Absorption of elemental iodine on the carbon in the particle appears to be less than or equal to 10 -4 μg I/g C. The fission-product-spectra excess of cesium over iodine would generally be adsorbed on the carbon, but may form Cs 2 MoO 4 under some circumstances

A 60-year record of 129I in Taal Lake sediments (Philippines): Influence of human nuclear activities at low latitude regions.

Science.gov (United States)

Zhang, Luyuan; Hou, Xiaolin; Li, Hong-Chun; Xu, Xiaomei

2018-02-01

The influence of human nuclear activities on environmental radioactivity is not well known at low latitude regions that are distant from nuclear test sites and nuclear facilities. A sediment core collected from Taal Lake in the central Philippines was analyzed for 129 I and 127 I to investigate this influence in a low-latitude terrestrial system. A baseline of 129 I/ 127 I atomic ratios was established at (2.04-5.14) × 10 -12 in the pre-nuclear era in this region. Controlled by the northeasterly equatorial trade winds, increased 129 I/ 127 I ratios of (20.1-69.3) × 10 -12 suggest that atmospheric nuclear weapons tests at the Pacific Proving Grounds in the central Pacific Ocean was the major source of 129 I in the sediment during 1956-1962. The 129 I/ 127 I ratios, up to 157.5 × 10 -12 after 1964, indicate a strong influence by European nuclear fuel reprocessing plants. The East Asian Winter Monsoon is found to be the dominant driving force in the atmospheric dispersion of radioactive iodine ( 129 I) from the European nuclear fuel reprocessing plants to Southeast Asia, which is also important for dispersion of other airborne pollutants from the middle-high to low latitude regions. A significant 129 I/ 127 I peak at 42.8 cm in the Taal Lake core appears to be the signal of the Chernobyl accident in 1986. In addition, volcanic activities are reflected in the iodine isotope profiles in the sediment core, suggesting the potential of using iodine isotopes as an indicator of volcanic eruptions. Copyright © 2017 Elsevier Ltd. All rights reserved.

Ceramic phases for immobilization of 129I

International Nuclear Information System (INIS)

Vance, E.R.; Agrawal, D.K.; Scheetz, B.E.; Pepin, J.G.; Atkinson, S.D.; White, W.B.

1981-01-01

Materials for ultimate disposal of 129 I have been studied. At present, iodide-sodalite, though not ideal, appears to be the best material for 129 I immobilization from the aspects of ease of preparation, thermal stability, cost of materials, and leach resistance. Good consolidation of the material was achieved by sintering in air at 1000 to 1200 0 C, but the iodine content was significantly below stoichiometric expectations. Hot aqueous media preferentially removed iodine, apparently by OH - substitution in near-neutral solutions, and I reversible reaction Cl - exchange occurred in brine. Alternation of the sodalite also took place. Soxhlet leach rates were about 5 x 10 -4 g/cm 2 -day by total weight loss, but physical weathering contributed significantly to this value. Moderate doses of radiation had no observable deleterious structural effects. Iodoboracites seemingly cannot be prepared by ceramic or nonhydrothermal wet chemical techniques. Fe-iodoboracite has inferior thermal stability to iodide-sodalite and was completely altered to hematite after treatment at 200 0 C in deionized water. Silver zeolites retained some iodine in the form of crystalline α-AgI at temperatures up to 1300 0 C even though heating above approx. 700 0 C altered the alumino-silicate framework. However, some of the iodine appeared to be present as soluble iodine, even in heated materials. Treatment at 200 0 C in deionized water or 2M NaCl significantly decreased the crystallinity of the aluminosilicate framework and the α-AgI reflections in the x-ray patterns were enhanced. Mild γ irradiations (approx. 50 MR) affected the x-ray diffraction patterns of some of the zeolites. Various lead oxyhalides had very poor thermal stability

Iodine-129 in Snow and Seawater in the Antarctic: Level and Source

DEFF Research Database (Denmark)

Xing, Shan; Hou, Xiaolin; Aldahan, Ala

2015-01-01

Anthropogenic 129I has been released to the environment in different ways and chemical species by human nuclear activities since the 1940s. These sources provide ideal tools to trace the dispersion of volatile pollutants in the atmosphere. Snow and seawater samples collected in Bellingshausen...... sites in the Southern Hemisphere. This feature indicates that 129I in Antarctic snow mainly originates from atmospheric nuclear weapons testing from 1945 to 1980; resuspension and re-emission of the fallout 129I in the Southern Hemisphere maintains the 129I level in the Antarctic atmosphere. 129I...

Chemical behavior of gaseous iodine at very low concentrations

International Nuclear Information System (INIS)

Lin, C.C.; Wang, C.F.; Yang, M.H.

2000-01-01

This paper summarizes the major results obtained in a research project investigating the behavior of iodine aerosols. This project includes laboratory studies on radiation effects of iodine in the gas phase and the measurements of airborne radioiodine in nuclear facilities. It was found that under gamma irradiation, the iodide (I - ) ions in aerosol were readily oxidized to I 2 and HIO, and some iodide ions were converted to organic iodine when organic additive was presented in the KI solution from which the aerosol was generated. The results also indicate that the behavior of irradiated iodide aerosol depends on the chemistry environment in both the carrier gas and the iodide solution. The chemical forms of airborne radioiodine in an isotope production laboratory and a nuclear power plant effluent have also been measured. Although radioiodine has been observed in various forms, the activity in organic forms was found to be the dominating species in both cases. (author)

Studies on the role of molybdenum on iodine transport in the RCS in nuclear severe accident conditions

International Nuclear Information System (INIS)

Grégoire, A.-C.; Kalilainen, J.; Cousin, F.; Mutelle, H.; Cantrel, L.; Auvinen, A.; Haste, T.; Sobanska, S.

2015-01-01

Highlights: • In oxidising conditions, Mo reacts with Cs and thus promotes gaseous iodine release. • In reducing conditions, CsI remains the dominant form for released iodine. • The nature of released iodine is well reproduced by the ASTEC code. - Abstract: The effect of molybdenum on iodine transport in the reactor coolant system (RCS) under PWR severe accident conditions was investigated in the framework of the EU SARNET project. Experiments were conducted at the VTT-Institute and at IRSN and simulations of the experimental results were performed with the ASTEC severe accident simulation code. As molybdenum affects caesium chemistry by formation of molybdates, it may have a significant impact on iodine transport in the RCS. Experimentally it has been shown that the formation of gaseous iodine is promoted in oxidising conditions, as caesium can be completely consumed to form caesium polymolybdates and is thus not available for reacting with gaseous iodine and leading to CsI aerosols. In reducing conditions, CsI remains the dominant form of iodine, as the amount of oxygen is not sufficient to allow formation of quantitative caesium polymolybdates. An I–Mo–Cs model has been developed and it reproduces well the experimental trends on iodine transport

Iodine-129 in the eastern Snake River Plain aquifer at and near the Idaho National Laboratory, Idaho, 2010-12

Science.gov (United States)

Bartholomay, Roy C.

2013-01-01

From 1953 to 1988, approximately 0.941 curies of iodine-129 (129I) were contained in wastewater generated at the Idaho National Laboratory (INL) with almost all of this wastewater discharged at or near the Idaho Nuclear Technology and Engineering Center (INTEC). Most of the wastewater containing 129I was discharged directly into the eastern Snake River Plain (ESRP) aquifer through a deep disposal well until 1984; lesser quantities also were discharged into unlined infiltration ponds or leaked from distribution systems below the INTEC. During 2010–12, the U.S. Geological Survey in cooperation with the U.S. Department of Energy collected groundwater samples for 129I from 62 wells in the ESRP aquifer to track concentration trends and changes for the carcinogenic radionuclide that has a 15.7 million-year half-life. Concentrations of 129I in the aquifer ranged from 0.0000013±0.0000005 to 1.02±0.04 picocuries per liter (pCi/L), and generally decreased in wells near the INTEC, relative to previous sampling events. The average concentration of 129I in groundwater from 15 wells sampled during four different sample periods decreased from 1.15 pCi/L in 1990–91 to 0.173 pCi/L in 2011–12. All but two wells within a 3-mile radius of the INTEC showed decreases in concentration, and all but one sample had concentrations less than the U.S. Environmental Protection Agency maximum contaminant level of 1 pCi/L. These decreases are attributed to the discontinuation of disposal of 129I in wastewater and to dilution and dispersion in the aquifer. The decreases in 129I concentrations, in areas around INTEC where concentrations increased between 2003 and 2007, were attributed to less recharge near INTEC either from less flow in the Big Lost River or from less local snowmelt and anthropogenic sources. Although wells near INTEC sampled in 2011–12 showed decreases in 129I concentrations compared with previously collected data, some wells south and east of the Central Facilities Area

Gas phase reactions of organic iodine in containment conditions

International Nuclear Information System (INIS)

Kaerkalae, T.; Holm, J.; Auvinen, A.; Zilliacus, R.; Kajolinna, T.; Tapper, U.; Gaenneskog, H.; Ekberg, C.

2010-01-01

In case of a hypothetical severe accident it is very likely that iodine at least partly deposits on painted walls of a reactor containment building. Iodine may react with painted surfaces to form organic iodine species. These organic species are a possible source of volatile iodine, which may increase the fraction of releasable iodine. Therefore, it is important to study the transport of organic iodine in containment conditions. Another question is, in which form are the organic iodides transported as gaseous molecules or as aerosol particles resulting from organic iodides reacting with radiolysis products. To answer this last question methyl iodide was fed into the EXSI facility in an air mixture. In some experiments the flow contained also humidity. The reactions took place in a quartz tube heated either to 50 deg. C, 90 deg. C or 120 deg. C. UV-light was used as a source of radiation to produce ozone from oxygen. A separate generator was also applied to reach higher ozone concentrations. Nucleated aerosol particles were collected on plane filters and gaseous iodine species were trapped in trapping bottles. Aerosol mass flow rate and size distribution as well as speciation of gaseous reaction products were measured with several on-line instruments. Collected aerosol particles were analysed with SEM. It was found that the formation of aerosol particles was very fast when ozone and methyl iodide were present in the facility. Even a very low concentration of ozone produced high number concentration of particles. The measured aerosol mass concentration increased with increasing temperature and ozone concentration. Because the particle diameter was quite small (<180 nm), their settling velocity is low. Therefore, iodine containing aerosols may exist in containment atmosphere for a long period of time. Part of methyl iodide was always transported through the facility regardless of experimental conditions. All ozone was consumed in the reactions when only UV-light was

Mechanisms of iodine release from iodoapatite in aqueous solution

Science.gov (United States)

Zhang, Z.; Wang, J.

2017-12-01

Immobilization of iodine-129 with waste forms in geological setting is challenging due to its extremely long half-life and high volatility in the environment. To evaluate the long-term performance of waste form, it is imperative to determine the release mechanism of iodine hosted in the waste form materials. This study investigated the iodine released from apatite structured waste form Pb9.85 (VO4)6 I1.7 to understand how diffusion and dissolution control the durability of apatite waste form. A standard semi-dynamic leach test was adopted in this study. Samples were exposed in fresh leachant periodically and the leachant was replaced after each interval. Each experiment was carried out in cap-sealed Teflon vessels under constant temperature (e.g. 90 °C). ICP-MS analysis on the reacted leachates shows that Pb and V were released constantly and congruently with the stoichiometric ratio of Pb/V. However, iodine release is incongruent and time dependent. The iodine release rate starts significantly higher than the corresponding stoichiometric value and gradually decreases, approaching the stoichiometric value. Therefore, a dual-mode mechanism is proposed to account for the iodine release from apatite, which is dominated by short-term diffusion and long-term dissolution processes. Additional tests show that the element release rates depend on a number of test parameters, including sample surface to solution volume ratio (m-1), interval (day), temperature (°C), and solution pH. This study provides a quantitative characterization of iodine release mechanism. The activation energy of iodine leaching 21±1.6 kJ/mol was obtained by varying the test temperature. At the test conditions of to neutral pH and 90 °C, the long-term iodine release rate 3.3 mg/(m2 • day) is projected by normalizing sample surface area to solution volume ratio (S/V) to 1.0 m-1 and interval to 1 day. These findings demonstrate i) the feasibility of our approach to quantify the release mechanism

Studies on 129I and 14C in environmental samples by AMS

International Nuclear Information System (INIS)

Muramatsu, Yasuyuki

2010-01-01

We have carried out studies on 129 I and 14 C in environmental samples by AMS (accelerator mass spectrometry). In this paper summary of our results are described. Iodine is an essential element for humans and it pays an important role in thyroid gland. There are more than 30 isotopes of iodine. Among radioiodines 129 I has the longest half-life (1.57x10 7 y). This nuclide is released into the environment from nuclear weapons test, accidents of nuclear facilities (e.g. Chernobyl accident) and operation of spent fuel reprocessing plants. Since soil accumulates iodine, we have focused on the levels of both 129 I and 127 I in surface soils. In our previous studies, we used NAA (neutron activation analysis) for the determination. However, due to the limitation of its analytical sensitivity we could not detect 129 I in samples from background areas. In this study we have analyzed 129 I/ 127 I ratios by AMS and 127 I concentrations by ICP-MS (inductively coupled plasma spectrometry) after separation of iodine from soil by pyrohydrolysis and solvent extraction techniques. Using these methods, we have analyzed samples collected from different areas in Japan. Analytical results for surface soils collected from background areas were in the ranges 1.4 x 10 -5 - 4.6 x 10 -3 Bq/Kg as 129 I concentrations and 3.9 x 10 -11 - 3.0 x 10 -8 as 129 I/ 127 I ratios. The 129 I levels in Tokaimura, where a spent fuel reprocessing plant is located, were one to three orders of magnitude higher than those in background samples. The levels were higher in forest soils than those in field and rice paddy soils due to the interception effect of atmospheric 129 I by tree canopies. A wide range of stable iodine concentrations (0.4-143ppm) was observed. Rice paddy soils contained significantly lower iodine than forest and upland field soils. This should be explained by the desorption of iodine from the rice paddies due to microbial activities during the cultivation. Vertical distributions of 129 I

A review of methods for immobilizing iodine-129 arising from a nuclear fuel recycle plant, with emphasis on waste-form chemistry

International Nuclear Information System (INIS)

Taylor, P.

1990-07-01

Possible methods for the separation and immobilization of iodine (mainly iodine-129) in a fuel recycle plant are reviewed, with special emphasis placed on the evaluation of waste forms. A distinction is drawn between waste forms selected by thermodynamic (solubility) or kinetic (dissolution rate) considerations. The most promising solubility-limited waste forms appear to be AgI (or AgI + AgCl) and a combination of Bi 2 O 3 and Bi 5 O 7 I. These materials use relatively scarce metals, Ag and Bi. They also have substantial chemical limitations, such as susceptibility to reductive dissolution and anion-displacement reactions; this calls for special care in the choice of a disposal site. All other organic iodides and iodates considered here and elsewhere appear to be still more limited in this respect. The most promising kinetically limited candidate waste form appears to be iodide-sodalite, but further information is needed on both the fabrication and leaching behaviour of this material. The possibility of disposal in a more soluble but isotopically dilute waste form, employing abundant raw materials, also warrants further consideration

Characterization of iodine species in the marine aerosol:to understand their roles in particle formation processes

Institute of Scientific and Technical Information of China (English)

Hongwei Chen; Rolf Brandt; Rolf Bandur; Thorsten Hoffmann

2006-01-01

In this contribution,iodine chemistry in the Marine Boundary Layer(MBL)is introduced.A series of methodologies for the measurements of iodine species in the gas and particle phases of the coastal atmosphere has been developed.Iodine species in the gas phase in real air samples has been determined in two field campaigns at the west coast of Ireland,indicating that gaseous iodo-hydrocarbons and elemental iodine are the precursors of new particle formation.Particulate iodine speciation from the same measurement campaigns show that the non-water-soluble iodine compounds are the main iodine species during the marine particle formation.A seaweed-chamber experiment was performed,indicating that gaseous I2 is one of the important precursors that lead to new particle formation in the presence of solar light in the ambient air at the coastal tidal area.

Iodine 129 concentration in river and lake water in the Fukushima area

International Nuclear Information System (INIS)

Tokuyama, Hironori; Matsuzaki, Hiroyuki; Miyake, Yasuto; Honda, Maki; Yamagata, Takeyasu

2012-01-01

A large amount of radionuclides, including "1"2"9I, were released into the environment by Fukushima Daiichi nuclear power plant accident. In determination of "1"2"9I, accelerator mass spectrometry is extraordinarily sensitive. We found that river and lake water in Fukushima area contained significant amount of "1"2"9I from the accident, and provided fruitful information for us. The concentration of "1"2"9I in the river and lake water taken in June 2012 ranged from 3.88 x 10"7 atoms/L to 3.32 x 10"9 atoms/L. The concentration of "1"2"9I in samples taken in Kawauchi village and Tamura city located in the west of the nuclear power plant was low, while that in Namie town, Iitate village and Minamisouma city was relatively high. In addition, the concentration of "1"2"9I in samples taken at the same place in December 2011, March 2012 and June 2012 was increased except one sample. This is result from the outflow of "1"2"9I which was attached to the organic matter, and from seasonal changes. To investigate the state of dilution of "1"2"9I in river and lake, it is necessary to take long-term and fixed-point observation. (author)

The retention of iodine by iodine filters in nuclear power plants in the case of fire (a literature review)

International Nuclear Information System (INIS)

Giraud, V.

1985-03-01

Due to the liberation of considerable amounts of gaseous combustion products, fires in nuclear power plants may lead to a deterioration in the retention of radioiodine by iodine filters. The combustion products of the burnable materials, i.e., insulations, lubricants and paints, vary considerably with the development of the fire. Combustion product analyses of these materials have been performed only to a limited extent. The reaction of iodine with combustion products as well as the retention of the resulting iodine reaction products by sorbents have not yet been investigated. The reduction in the removal efficiencies of iodine sorbents due to the presence of combustion products is unknown. (orig.) [de

Gaseous radioiodine transport in the air-forage-cow-milk system

International Nuclear Information System (INIS)

Black, S.C.; Douglas, R.L.; Barth, D.S.

1976-04-01

To study the transport of 131 I in the air-forage-cow milk system, a gaseous form of 131 I was released over a field of growing alfalfa which also contained some baled hay and dairy cows in pens. Some of the alfalfa was converted to hay and fed to cows, and some was used as green chop for other cows and goats. The results of this experiment suggest that the deposition velocity of gaseous iodine is much less than that for iodine bound to particulates; that cows ingesting hay secrete a higher percentage of 131 I in milk than cows ingesting green chop; that gaseous forms do not penetrate hay bales to any great extent; that the gaseous form is transferred to milk in a manner similar to particulate forms; that ingestion of contaminated forage results in 80 times as much 131 I transfer to milk as does inhalation exposure to the same cloud; and that goats transfer 131 I from forage to milk more efficiently than do dairy cows

Determination of "1"2"9I using volatilization method and liquid scintillation spectrometry

International Nuclear Information System (INIS)

Remenec, Boris; Dulanska, Silvia; Horvathova, Bianka; Matel, Lubomir

2017-01-01

A simple and rapid separation method for "1"2"9I determination in radioactive waste samples was developed. Suitable conditions for iodine volatilization were tested. Iodine was trapped in 1.5 mol L"-"1 NaOH and precipitated as PdI_2·H_2O by addition of PdCl_2 with recoveries higher than 80%. The method was applied for analysis of contaminated soil, radioactive sludge, evaporator concentrate and heterogeneous waste samples from nuclear power plants in Slovak Republic. "1"2"9I was measured on liquid scintillation counter TRI CARB 2900 TR using Ultima Gold AB scintillation cocktail. (author)

Estimating permissible /sup 129/I-emission rates

Energy Technology Data Exchange (ETDEWEB)

Huebschmann, W G

1976-06-01

A mathematical method of iodine release limitation is presented which, in assessing the radiological effectiveness of /sup 129/I, takes advantage of the fact that the chemical behaviour of /sup 129/I resembles that of /sup 131/I and relies on the already extensive knowledge of the chemical and biological behaviour of /sup 131/I. If this method is used for calculating permissible /sup 129/I emission rates it is stated that no unnecessary restrictions need be imposed on a fuel reprocessing plant and that the grazing season for the pasture-cow-milk pathway can be taken into account. The concept is currently in use at the Karlsruhe Nuclear Research Center and seems to be appropriate for licensing of nuclear fuel reprocessing plants.

Pool scrubbing models for iodine components

Energy Technology Data Exchange (ETDEWEB)

Fischer, K [Battelle Ingenieurtechnik GmbH, Eschborn (Germany)

1996-12-01

Pool scrubbing is an important mechanism to retain radioactive fission products from being carried into the containment atmosphere or into the secondary piping system. A number of models and computer codes has been developed to predict the retention of aerosols and fission product vapours that are released from the core and injected into water pools of BWR and PWR type reactors during severe accidents. Important codes in this field are BUSCA, SPARC and SUPRA. The present paper summarizes the models for scrubbing of gaseous Iodine components in these codes, discusses the experimental validation, and gives an assessment of the state of knowledge reached and the open questions which persist. The retention of gaseous Iodine components is modelled by the various codes in a very heterogeneous manner. Differences show up in the chemical species considered, the treatment of mass transfer boundary layers on the gaseous and liquid sides, the gas-liquid interface geometry, calculation of equilibrium concentrations and numerical procedures. Especially important is the determination of the pool water pH value. This value is affected by basic aerosols deposited in the water, e.g. Cesium and Rubidium compounds. A consistent model requires a mass balance of these compounds in the pool, thus effectively coupling the pool scrubbing phenomena of aerosols and gaseous Iodine species. Since the water pool conditions are also affected by drainage flow of condensate water from different regions in the containment, and desorption of dissolved gases on the pool surface is determined by the gas concentrations above the pool, some basic limitations of specialized pool scrubbing codes are given. The paper draws conclusions about the necessity of coupling between containment thermal-hydraulics and pool scrubbing models, and proposes ways of further simulation model development in order to improve source term predictions. (author) 2 tabs., refs.

Pool scrubbing models for iodine components

International Nuclear Information System (INIS)

Fischer, K.

1996-01-01

Pool scrubbing is an important mechanism to retain radioactive fission products from being carried into the containment atmosphere or into the secondary piping system. A number of models and computer codes has been developed to predict the retention of aerosols and fission product vapours that are released from the core and injected into water pools of BWR and PWR type reactors during severe accidents. Important codes in this field are BUSCA, SPARC and SUPRA. The present paper summarizes the models for scrubbing of gaseous Iodine components in these codes, discusses the experimental validation, and gives an assessment of the state of knowledge reached and the open questions which persist. The retention of gaseous Iodine components is modelled by the various codes in a very heterogeneous manner. Differences show up in the chemical species considered, the treatment of mass transfer boundary layers on the gaseous and liquid sides, the gas-liquid interface geometry, calculation of equilibrium concentrations and numerical procedures. Especially important is the determination of the pool water pH value. This value is affected by basic aerosols deposited in the water, e.g. Cesium and Rubidium compounds. A consistent model requires a mass balance of these compounds in the pool, thus effectively coupling the pool scrubbing phenomena of aerosols and gaseous Iodine species. Since the water pool conditions are also affected by drainage flow of condensate water from different regions in the containment, and desorption of dissolved gases on the pool surface is determined by the gas concentrations above the pool, some basic limitations of specialized pool scrubbing codes are given. The paper draws conclusions about the necessity of coupling between containment thermal-hydraulics and pool scrubbing models, and proposes ways of further simulation model development in order to improve source term predictions. (author) 2 tabs., refs

Iodide and iodate (129I and 127I) in surface water of the Baltic Sea, Kattegat and Skagerrak

DEFF Research Database (Denmark)

Hansen, Violeta; Yi, Peng; Hou, Xiaolin

2011-01-01

Despite the common incorporation of iodine in the biological cycle and occurrence of huge contamination of the radioactive isotope 129I in the Baltic Proper, Skagerrak and Kattegat, there is no data on chemical speciation of iodine in these waters. We here present first time data on iodine isotopes...

Experimental and modelling studies of iodine oxide formation and aerosol behaviour relevant to nuclear reactor accidents

International Nuclear Information System (INIS)

Dickinson, S.; Auvinen, A.; Ammar, Y.; Bosland, L.; Clément, B.; Funke, F.; Glowa, G.; Kärkelä, T.; Powers, D.A.; Tietze, S.; Weber, G.; Zhang, S.

2014-01-01

Highlights: • Radiolytic reactions can influence iodine volatility following a nuclear accident. • Kinetic models have been developed based on atmospheric chemistry studies. • Properties of iodine oxide aerosols produced by radiation have been measured. • Decomposition of iodine oxides by the action of heat or radiation has been observed. - Abstract: Plant assessments have shown that iodine contributes significantly to the source term for a range of accident scenarios. Iodine has a complex chemistry that determines its chemical form and, consequently, its volatility in the containment. If volatile iodine species are formed by reactions in the containment, they will be subject to radiolytic reactions in the atmosphere, resulting in the conversion of the gaseous species into involatile iodine oxides, which may deposit on surfaces or re-dissolve in water pools. The concentration of airborne iodine in the containment will, therefore, be determined by the balance between the reactions contributing to the formation and destruction of volatile species, as well as by the physico-chemical properties of the iodine oxide aerosols which will influence their longevity in the atmosphere. This paper summarises the work that has been done in the framework of the EC SARNET (Severe Accident Research Network) to develop a greater understanding of the reactions of gaseous iodine species in irradiated air/steam atmospheres, and the nature and behaviour of the reaction products. This work has mainly been focussed on investigating the nature and behaviour of iodine oxide aerosols, but earlier work by members of the SARNET group on gaseous reaction rates is also discussed to place the more recent work into context

Iodine-129 and Caesium-137 in Chernobyl contaminated soil and their chemical fractionation

DEFF Research Database (Denmark)

Hou, Xiaolin; Fogh, C.L.; Kucera, J.

2003-01-01

Soil samples from areas in Belarus, Russia and Sweden contaminated by the Chernobyl accident were analysed for I-129 by radiochemical neutron activation analysis, as well as for Cs-137 by gamma-spectrometry. The atomic ratio of I-129/(CS)-C-137 in the upper layer of the examined soil cores ranged...... from 0.10 to 0.30, with an average of 0.18, and no correlation between I-129/Cs-137 ratio and the distance from Chernobyl reactor to sampling location was observed. It seems feasible to use the I-129/Cs-137 ratio to reconstruct the deposition pattern of I-131 in these areas. The association of I-129...... and (CS)-C-137 in the Chernobyl soil and Irish Sea sediment was investigated by a sequential extraction method. Similar speciation of I-129 in the Chernobyl soil and Irish Sea sediment was found. Approximately 70% of I-129 is bound to oxides and organic matter, and 10-20% is in the readily available phase...

Environmental behavior and effects of technetium-99 and iodine-129

International Nuclear Information System (INIS)

Garland, T.R.; Schreckhise, R.G.; Wildung, R.E.; Cadwell, L.L.; McFadden, K.M.; Cataldo, D.A.

1980-01-01

The objective of this program is to define the environmental behavior of 99 Tc and 129 I, two long-lived radioactive by-products of the nuclear fuel cycle that have received little study. The specific objectives are to (1) determine the soil physicochemical and microbiological factors and physiological parameters that govern the mobility and bioavailability of different chemical forms of 99 Tc and 129 I in terrestrial and aquatic environments and (2) validate and measure food web transport in selected field locations

Biofortification of lettuce (Lactuca sativa L.) with iodine: the effect of iodine form and concentration in the nutrient solution on growth, development and iodine uptake of lettuce grown in water culture.

Science.gov (United States)

Voogt, Wim; Holwerda, Harmen T; Khodabaks, Rashied

2010-04-15

Iodine is an essential trace element for humans. Two billion individuals have insufficient iodine intake. Biofortification of vegetables with iodine offers an excellent opportunity to increase iodine intake by humans. The main aim was to study the effect of iodine form and concentration in the nutrient solution on growth, development and iodine uptake of lettuce, grown in water culture. In both a winter and summer trial, dose rates of 0, 13, 39, 65, and 90 or 129 microg iodine L(-1), applied as iodate (IO(3)(-)) or iodide (I(-)), did not affect plant biomass, produce quality or water uptake. Increases in iodine concentration significantly enhanced iodine content in the plant. Iodine contents in plant tissue were up to five times higher with I(-) than with IO(3)(-). Iodine was mainly distributed to the outer leaves. The highest iodide dose rates in both trials resulted in 653 and 764 microg iodine kg(-1) total leaf fresh weight. Biofortification of lettuce with iodine is easily applicable in a hydroponic growing system, both with I(-) and IO(3)(-). I(-) was more effective than IO(3)(-). Fifty grams of iodine-biofortified lettuce would provide, respectively, 22% and 25% of the recommended daily allowance of iodine for adolescents and adults. (c) 2010 Society of Chemical Industry.

Speciation Analysis of ¹²⁹I and ¹²⁷I in Aerosols Using Sequential Extraction and Mass Spectrometry Detection

DEFF Research Database (Denmark)

Zhang, Luyuan; Hou, Xiaolin; Xu, Sheng

2015-01-01

A new analytical method has been developed for speciation analysis of 127I and 129I in aerosols collected on polypropylene (PP) filter paper. Iodide, iodate, NaOH soluble iodine, and insoluble iodine were separated from aerosols using sequential extraction, chromatography separation, and alkaline...... ashing and measured using inductive coupled plasma mass spectrometry (ICP-MS) for 127I and accelerator mass spectrometry (AMS) for 129I. Parameters affecting the leaching efficiency and stability of iodine species, such as leaching time and temperature, amount of alkaline reagent for ashing, ashing...... temperature and time, and iodine protective agent, were investigated and optimized. It was observed that long time water leaching would change inorganic iodine species due to photochemical oxidation of iodide on the PP filter surface. NaOH leaching can only extract less than 60% of iodine from the studied...

Chemical Speciation Analysis and Environmental Behaviour of ¹²⁷I and ¹²⁹I

DEFF Research Database (Denmark)

Hansen, Violeta

2011-01-01

may be a slow process while along the Baltic Sea surface water reduction of iodate is a relatively fast process. Although suboxic or anoxic condition are encountered in some of the Baltic Sea deep basins, the concentration of 129IO3 - increases with water depth indicating that the reduction of iodate......) in environmental samples are very complex and strongly dependent on several factors, such as water/soil/sediment chemistry, seaweed type, different pH, Eh, quantity and quality of organic matter, microbiological activity as well as differences in contaminant origin. The 129I isotope, where the main inventory has...... in the oxygen deficient bottom water of the Baltic Sea is a slow process. Iodine chemical speciation analysis (as iodide, iodate and total iodine including inorganic and organic iodine species) in lake water samples collected from Denmark and southern Sweden has been carried out. Destruction of organic iodine...

{sup 127}I and {sup 129}I/{sup 127}I isotopic ratio in marine alga Fucus virsoides from the North Adriatic Sea

Energy Technology Data Exchange (ETDEWEB)

Osterc, Andrej [Department of Environmental Sciences, Jozef Stefan Institute, Jamova 39, 1000 Ljubljana (Slovenia); Stibilj, Vekoslava [Department of Environmental Sciences, Jozef Stefan Institute, Jamova 39, 1000 Ljubljana (Slovenia)], E-mail: vekoslava.stibilj@ijs.si

2008-04-15

The only stable iodine isotope is {sup 127}I and the natural {sup 129}I/{sup 127}I ratio in the biosphere has increased from 10{sup -15}-10{sup -14} to 10{sup -10}-10{sup -9}, mainly due to emissions from nuclear fuel reprocessing plants. In Europe they are located at La Hague (France) and Sellafield (England), where the ratio of {sup 129}I/{sup 127}I is up to 10{sup -4}. The marine environment, i.e. the oceans, is the major source of iodine with average concentrations of around 60 {mu}g L{sup -1} iodine in seawater. Brown algae accumulate iodine at high levels of up to 1.0% of dry weight, and therefore they are an ideal bioindicator for studying the levels of {sup 127}I and {sup 129}I in the marine environment. A radiochemical neutron activation analysis (RNAA) method, developed at our laboratory, was used for {sup 129}I determination in the brown alga Fucus virsoides (Donati) J. Agardh, and the same technique of RNAA was used for total {sup 127}I determination. The samples were collected along the coast of the Gulf of Trieste and the West coast of Istria in the North Adriatic Sea in the period from 2005 to 2006. Values of the {sup 129}I/{sup 127}I ratio up to 10{sup -9} were found, which is in agreement with the present average global distribution of {sup 129}I. The levels of stable iodine found were in the range from 235 to 506 {mu}g g{sup -1} and the levels of {sup 129}I from 1.7 to 7.3 x 10{sup -3} Bq kg{sup -1} (2.6-10.9 x 10{sup -7} {mu}g g{sup -1}), on a dry matter basis.

Leaching of iodine from composites based on epoxy resin and lead iodide

International Nuclear Information System (INIS)

Kalinin, N.N.; Elizarova, A.N.

1988-01-01

The scope for using solid composites obtained by incorporating dry powdery lead iodide and its aqueous suspension into epoxy resin for prolonged immobilization of iodine-129 under monitorable storage conditions has been assessed by a study of leaching of iodine

Is it necessary to transmute 129I?

International Nuclear Information System (INIS)

Nifenecker, H.; Brissot, R.

2001-01-01

129 I is the unstable fission product with the record half life of 15.7 million years. It is produced with a yield of 0.7% in the thermal neutron induced fission of 235 U. Typically, a 1 GWe PWR reactor produces about 4 kg of 129 I annually. Iodine is highly soluble in water, and that property compounded with its very long half life makes 129 I the isotope most likely to leak through the biosphere from a deep underground storage site. In fact it is highly probable that it will be incorporated in the biosphere before it decays. Therefore, at least for the far future, sequestration in deep underground sites is no more justified than direct and immediate dispersion into the environment. It is, thus, important to know at which level of deployment of nuclear power the diffusion of 129 I in the biosphere might be a hazard for living beings at any time in the future. (authors)

Iodine-129 in the Snake River Plain Aquifer at and Near the Idaho National Laboratory, Idaho, 2003 and 2007

Science.gov (United States)

Bartholomay, Roy C.

2009-01-01

From 1953 to 1988, wastewater containing approximately 0.94 curies of iodine-129 (129I) was generated at the Idaho National Laboratory (INL) in southeastern Idaho. Almost all of this wastewater was discharged at or near the Idaho Nuclear Technology and Engineering Center (INTEC) on the INL site. Most of the wastewater was discharged directly into the eastern Snake River Plain aquifer through a deep disposal well until 1984; however, some wastewater also was discharged into unlined infiltration ponds or leaked from distribution systems below the INTEC. In 2003, the U.S. Geological Survey (USGS), in cooperation with the U.S. Department of Energy, collected samples for 129I from 36 wells used to monitor the Snake River Plain aquifer, and from one well used to monitor a perched zone at the INTEC. Concentrations of 129I in the aquifer ranged from 0.0000066 +- 0.0000002 to 0.72 +- 0.051 picocuries per liter (pCi/L). Many wells within a 3-mile radius of the INTEC showed decreases of as much as one order of magnitude in concentration from samples collected during 1990-91, and all of the samples had concentrations less than the Environmental Protection Agency's Maximum Contaminant Level (MCL) of 1 pCi/L. The average concentration of 129I in 19 wells sampled during both collection periods decreased from 0.975 pCi/L in 1990-91 to 0.249 pCi/L in 2003. These decreases are attributed to the discontinuation of disposal of 129I in wastewater after 1988 and to dilution and dispersion in the aquifer. Although water from wells sampled in 2003 near the INTEC showed decreases in concentrations of 129I compared with data collected in 1990-91, some wells south and east of the Central Facilities Area, near the site boundary, and south of the INL showed slight increases. These slight increases may be related to variable discharge rates of wastewater that eventually moved to these well locations as a mass of water from a particular disposal period. In 2007, the USGS collected samples for

High purity zirconium obtainment through the iodine compounds transport method

International Nuclear Information System (INIS)

Bolcich, J.C.; Zuzek, E.; Dutrus, S.M.; Corso, H.L.

1987-01-01

This paper describes the experimental method and the equipment designed, constructed and actually applied for the high purity zirconium obtainment from a zirconium sponge of the nuclear type. The mechanism of purification is based on the impure metal attack with gaseous iodine (at 200 deg C) to obtain zirconium tetra iodine as main product which is then transformed into a pure zirconium base (at 1000-1300 deg C), precipitating the metallic zirconium and releasing the gaseous iodine. From the first experiences carried out, pure zirconium has been obtained from an initial filament of 0.5 mm of diameter as well as wires up to 2.5 mm of diameter. This work presents the results from the studies and analysis made to characterize the material obtained. Finally, the refining methods to which the zirconium produced may be submitted so as to optimize the final purity are discussed. (Author)

Speciation analysis of I-127,129 in the crop field soil contaminated by the Fukushima Dai-ichi nuclear power plant accident with newly developed chemical separation techniques

Science.gov (United States)

Honda, Maki; Matsuzaki, Hiroyuki; Saito, Takumi; Nagai, Hisao

2014-05-01

In previous study, we investigated the depth profile of the accident derived I-129 and downward migration speed in soils of near-field of Fukushima Dai-ichi Nuclear Power Plant, including crop fields and man-made fields. I-129 in soil was measured by AMS and stable iodine (I-127) was measured by ICP-MS at MALT (Micro Analysis Laboratory, Tandem accelerator), The University of Tokyo. It was found that I-129 was concentrated near surface but distributed deeper compared with Cs-137. It was also found that I-129 seems to move downward more quickly than Cs-137. To investigate the adsorption mechanism and the elemental process of migration of the accident derived I-129 in soil, it is important to know what kind of component the I-129 combines with. Recent studies on the X-ray absorption fine structure (XAFS), especially near edge structure (XANES), reported that the stable iodine (I-127) in soil existed as an organic component. However, it had not yet been proved that it was also the case with the accident derived I-129 because it had been incorporated in the soil system only recently and the abundance of I-129 in soil was more than 8 orders of magnitude smaller than sub-ppm level stable iodine (I-127). In this study a progressive sequential extraction method including the dialysis and the dynamic headspace method was newly developed to obtain only the iodine sticking to the soil organic component. The stable iodine can be quantified by direct analysis of the fraction and I-129 can be quantified by AMS method of the fraction added with carrier. The fraction of the organic component for I-127 and I-129 can be evaluated respectively by comparing with the other fraction and/or with the total concentration obtained by the bulk analysis (e.g. by the pyrohydrolysis).

IODINE REMOVAL EFFICIENCY IN NON-SUBMERGED AND SUBMERGED SELF-PRIMING VENTURI SCRUBBER

OpenAIRE

MAJID ALI; YAN CHANGQI; SUN ZHONGNING; GU HAIFENG; WANG JUNLONG; KHURRAM MEHBOOB

2013-01-01

The objective of this conducted research is to study the iodine removal efficiency in a self-priming venturi scrubber for submerged and non-submerged operating conditions experimentally and theoretically. The alkaline solution is used as an absorbent, which is prepared by dissolving sodium hydroxide (NaOH) and sodium thiosulphate (Na2S2O3) in water to remove the gaseous iodine (I2) from the gas. Iodine removal efficiency is examined at various gas flow rates and inlet concentrations of iodine...

Two-layer type filter for removal of radioactive iodine

Energy Technology Data Exchange (ETDEWEB)

Taoki, M

1976-04-16

The object is to provide a filter for removing radioactive iodine, which is used for disposal of gaseous waste in an atomic power plant, to particularly hold a pressure loss lower. The filter according to the present invention comprises two layers, which are filled at a front stage with active carbon, which is small in pressure loss and has a good collective efficiency relative to iodine, and at a rear stage with silver zeolite, which has a good collective efficiency relative to both iodine and methyl iodine, whereby respective adsorbent are effectively utilized to minimize pressure loss even if a large quantity of air.

Two-layer type filter for removal of radioactive iodine

International Nuclear Information System (INIS)

Taoki, Masafumi.

1976-01-01

Object: To provide a filter for removing radioactive iodine, which is used for disposal of gaseous waste in an atomic power plant, to particularly hold a pressure loss lower. Structure: The filter according to the present invention comprises two layers, which are filled at a front stage with active carbon, which is small in pressure loss and has a good collective efficiency relative to iodine, and at a rear stage with silver zeolite, which has a good collective efficiency relative to both iodine and methyl iodine, whereby respective adsorbent are effectively utilized to minimize pressure loss even if a large quantity of air. (Kamimura, M.)

Iodine Status and Iodised Salt Consumption in Portuguese School-Aged Children: The Iogeneration Study.

Science.gov (United States)

Costa Leite, João; Keating, Elisa; Pestana, Diogo; Cruz Fernandes, Virgínia; Maia, Maria Luz; Norberto, Sónia; Pinto, Edgar; Moreira-Rosário, André; Sintra, Diana; Moreira, Bárbara; Costa, Ana; Silva, Sofia; Costa, Vera; Martins, Inês; Castro Mendes, Francisca; Queirós, Pedro; Peixoto, Bruno; Carlos Caldas, José; Guerra, António; Fontoura, Manuel; Leal, Sandra; Moreira, Roxana; Palmares Carvalho, Irene; Matias Lima, Rui; Martins, Catia; Delerue-Matos, Cristina; Almeida, Agostinho; Azevedo, Luís; Calhau, Conceição

2017-05-05

The World Health Organization promotes salt iodisation to control iodine deficiency. In Portugal, the use of iodised salt in school canteens has been mandatory since 2013. The present study aimed to evaluate iodine status in school-aged children (6-12 years) and to monitor the use of iodised salt in school canteens. A total of 2018 participants were randomly selected to participate in a cross-sectional survey in northern Portugal. Children's urine and salt samples from households and school canteens were collected. A lifestyle questionnaire was completed by parents to assess children's eating frequency of iodine food sources. Urinary iodine concentration (UIC) was measured by inductively coupled plasma-mass spectrometry. The median UIC was 129 µg/L which indicates the adequacy of iodine status and 32% of the children had UIC < 100 µg/L. No school canteen implemented the iodised salt policy and only 2% of the households were using iodised salt. Lower consumption of milk, but not fish, was associated with a higher risk of iodine deficiency. Estimation of sodium intake from spot urine samples could be an opportunity for adequate monitoring of population means. Implementation of iodine deficiency control policies should include a monitoring program aligned with the commitment of reducing the population salt intake.

Speciation analysis of 129I in seawater by carrier-free AgI-AgCl coprecipitation and accelerator mass spectrometric measurement

DEFF Research Database (Denmark)

Luo, Maoyi; Hou, Xiaolin; He, Chaohui

2013-01-01

A rapid and simple method was developed for speciation analysis of 129I in seawater by selective coprecipitation of carrier-free iodide and accelerator mass spectrometry (AMS) measurement of 129I. Iodide was separated from seawater and other species of iodine by coprecipitation of AgI with Ag2SO3......, AgCl, and AgBr by addition of only 100 mg/L Ag+ and 0.3 mmol/L NaHSO3 at pH 4.2-5.5. The separation efficiency of iodide was more than 95%, and crossover between 129IO3- and 129I- fractions is less than 3%. Iodate and total inorganic iodine were converted to iodide by use of NaHSO3 at pH 1......-2 and then separated by the same method as for iodide. Ag2SO3 in the coprecipitate was removed by washing with 3 mol/L HNO3 and the excess AgCl and AgBr was removed by use of diluted NH3, and finally a 1-3 mg precipitate was obtained for AMS measurement of 129I. The recovery of iodine species in the entire procedure...

Retention of gaseous fission products in reprocessing LMFBR fuels

International Nuclear Information System (INIS)

Burch, W.D.; Yarbro, O.O.; Groenier, W.S.; Stephenson, M.J.

1976-05-01

The report is devoted to status of the development programme at the Oak Ridge National Laboratory on methods for retaining iodine-131 and 129, Krypton-85, Tritium and Carbon-14 in reprocessing LMFBR fuels. The Iodox process, Fluorocarbon absorption process and Voloxidation process are described for retention of iodine, Krypton-85 and Tritium, respectively. Flowsheets for the different processes are given and results of experimental runs in small engineering-scale equipment are reported

Methods of I-129 analysis for environmental monitoring

International Nuclear Information System (INIS)

Nomura, T.; Katagiri, H.; Kitahara, Y.; Fukuda, S.

1980-01-01

Among the radioiodine isotopes discharged from nuclear facilities, I-129 has the longest half-life (1.7 x 10 7 years) and thus environmental monitoring of this nuclide is important. Methods of analysis of low level I-129 in environmental samples such as milk, crops, seaweeds and soils are described. The iodine is separated from the dried or pulverized samples by ignition at 1000 0 C in a quartz combustion apparatus with a stream of oxygen. Stable I-127 is simultaneously determined and the atom ratio of 129 I/ 127 I calculated in order to evaluate the thyroid dose by the specific activity method. Results of an analysis of typical food samples collected near the fuel reprocessing plant of Tokai Works showed no I-129 concentrations higher than the detection limit of the method (10 -2 pCi for 10 g. dry sample). (UK)

A denuder-impinger system with in situ derivatization followed by gas chromatography-mass spectrometry for the determination of gaseous iodine-containing halogen species.

Science.gov (United States)

Huang, Ru-Jin; Hoffmann, Thorsten

2008-11-14

Reactive iodine species have been suggested to play an important role in the atmosphere (e.g. tropospheric ozone depletion, coastal new particle formation). However, there still exist major uncertainties about their atmospheric chemistry, mostly due to the lack of analytical approaches for the accurate speciation of certain key compounds. In this study, 1,3,5-trimethoxybenzene (1,3,5-TMB)-coated denuder proved to be suitable for the differentiation between gaseous interhalogens (iodine monochloride (ICl), iodine monobromide (IBr)) and molecular iodine (I2) based on a selective collection/derivatization method. The results of the denuder sampling were compared with the results of impinger sampling in water, methanol and carbon tetrachloride solutions of 1,3,5-TMB. ICl and IBr are converted into 1-iodo-2,4,6-trimethoxybenzene (1-iodo-2,4,6-TMB) and 1-bromo-2,4,6-trimethoxybenzene (1-bromo-2,4,6-TMB), respectively, in the denuder systems. The respective collection efficiency is 99.2% for ICl and 92.6% for IBr, at 500mLmin(-1) gas flow rate. The collection efficiency for I2 is lower than 1% in the same denuder system, but significantly increases to about 90% in the aqueous 1,3,5-TMB loaded impinger. The denuder-impinger coupled system was then used to differentiate and to collect the ICl, IBr and I2 gas mixtures, followed by gas chromatography-ion trap mass spectrometry (GC-MS) determination. The precision of the method is in general better than 9.1%. The parameters affecting denuder operation including sampling flow rate, sampling duration, and relative humidity have been evaluated. The presented method provides an attractive protocol for iodine species analysis for atmospheric chemistry research.

Immobilization and bonding scheme of radioactive iodine-129 in silver tellurite glass

Science.gov (United States)

Lee, Cheong Won; Pyo, Jae-Young; Park, Hwan-Seo; Yang, Jae Hwan; Heo, Jong

2017-08-01

Silver tellurite glasses with melting temperatures disposal site. Iodine waste loading in glasses was as high as 12.64 wt% of all metallic elements and 11.21 wt% including oxygen. Normalized elemental releases obtained from the product consistency test were well below US regulation of 2 g/m2. Iodines are surrounded by four Ag+ ions forming [Ag4I]3+ units that are further connected to tellurite network through bonds with non-bridging oxygens.

New Resin for the Selective Extraction of {sup 129}I

Energy Technology Data Exchange (ETDEWEB)

Bombard, A.; Happel, S. [TrisKem International, Bruz (France); Zulauf, A. [NUKEM Technologies GmbH, Alzenau (Germany); Streng, R. [Radiochemistry, Department of Chemistry, Philipps-University Marburg, Marburg (Germany)

2013-07-15

{sup 129}I is an ideal tracer of the marine environment. It has been used for some years particularly in the northeast Atlantic, Nordic seas and Arctic to determine its distribution after its discharges from La Hague and Sellafield reprocessing plants. Various methods for {sup 129}I determination exist. A new resin selective for iodine has been developed, characterized and tested on environmental samples. In order to allow {sup 129}I determination and to obtain accurate and precise results, the samples have to pass a number of sample preparation steps; among these steps are chemical separation and purification. The results of the analysis of seawater samples are presented. (author)

Distribution of Iodine-129 in off the coast of Fukushima and North Pacific

International Nuclear Information System (INIS)

Hasegawa, A.; Yamagata, T.; Nagai, H.; Aoyama, M.; Matsuzaki, H.

2013-01-01

We measured "1"2"9I concentration in seawater samples which were collected in off Fukushima and North Pacific. High "1"2"9I concentrations were observed in samples from stations off Fukushima (BD02, 03) located 30 km away from Fukushima Dai-ichi Nuclear Power Plant (F1NPP). In these stations, "1"2"9I inventory down to 100 m water depth was not decrease since three month after the F1NPP accident. In adjacent stations off Fukushima (BD01, 04), "1"2"9I concentrations were almost identical to those observed in seawater collected in the Kuroshio region before the F1NPP accident. In the North Pacific (BD05∼17), "1"2"9I concentrations in surface seawater were 2 times higher than those in the Kuroshio region. (author)

The 129iodine bomb pulse recorded in Mississippi River Delta sediments: results from isotopes of I, Pu, Cs, Pb, and C

Science.gov (United States)

Oktay, S. D.; Santschi, P. H.; Moran, J. E.; Sharma, P.

2000-03-01

129I ( t1/2 = 1.56 × 10 7 yr) has both natural as well as anthropogenic sources. Anthropogenic sources from nuclear reprocessing discharges and bomb test fallout have completely overwhelmed the natural signal on the surface of the earth in the last 50 years. However, the transfer functions in and out of environmental compartments are not well known due to temporal variations in the sources of 129I and to a lack of knowledge regarding the forms of iodine. From a vertical profile of 129I/ 127I ratios in sediments located in the Mississippi Delta region in approximately 60 meters water depth, the 129I input function to this region was reconstructed. Dates in the core were assigned based on the plutonium peak at 20 cm depth (assumed to have been deposited in 1963) and the excess 210Pb profile in the same depth interval, and below that, based on the steadily decreasing 240Pu/ 239Pu ratios from a ratio of 0.18 at 22 cm to 0.05 at 57 cm depth, the 1953 horizon. These low 240Pu/ 239Pu values are attributed to low yield, close-in, tropospherically transported bomb fallout produced from the Nevada test site in the early 1950s, which had a value of about 0.035, and strongly suggest a terrestrial source for Pu isotopes. 129I/ 127I ratios increased from 2 × 10 -10 at 3 cm to 4 × 10 -10 at 20 cm, and from there decreased monotonously to pre-anthropogenic values at 53 cm and below. 129I concentrations ranged from 8-13 × 10 6 atoms/g in the top 20 cm, and decreased to values of less than 1 × 10 6 atoms/g below 50 cm. Atom ratios of 129I/ 137Cs, decay corrected to 1962, the year of maximum radionuclide production, are about 0.3, very close to the production ratios of about 0.2 during atomic bomb tests. This evidence, combined with other observations, strongly suggests that 129I in Mississippi River Delta sediments originates from atomic bomb fallout eroded from soils of the Mississippi River drainage basin, with little alteration of the isotopic ratios during transport from

Irradiation and gamma-ray spectrometric parameters for 129I neutron-activation analysis

International Nuclear Information System (INIS)

Brauer, F.P.; Strebin, R.S. Jr.; Mitzlaff, W.A.; Kaye, J.H.

1983-09-01

This paper describes the influence of reactor neutron irradiation facilities on low-level 129 I analysis methodology. Three reactors are compared - the HFIR at ORNL, the N-Reactor at Hanford, and a 1-MW research reactor at Washington State University, Pullman, WA. Parameters compared include sensitivity for 129 I and natural iodine and interference effects due to high levels of 127 I in irradiated samples. Selection of detector systems for off-site use at HFIR is discussed. A comparison of neutron activation analysis with other sensitive detection methods for measurement of 129 I is given

Uptake and distribution of organo-iodine in deep-sea corals.

Science.gov (United States)

Prouty, Nancy G; Roark, E Brendan; Mohon, Leslye M; Chang, Ching-Chih

2018-07-01

Understanding iodine concentration, transport, and bioavailability is essential in evaluating iodine's impact to the environment and its effectiveness as an environmental biogeotracer. While iodine and its radionuclides have proven to be important tracers in geologic and biologic studies, little is known about transport of this element to the deep sea and subsequent uptake in deep-sea coral habitats. Results presented here on deep-sea black coral iodine speciation and iodine isotope variability provides key information on iodine behavior in natural and anthropogenic environments, and its geochemical pathway in the Gulf of Mexico. Organo-iodine is the dominant iodine species in the black corals, demonstrating that binding of iodine to organic matter plays an important role in the transport and transfer of iodine to the deep-sea corals. The identification of growth bands captured in high-resolution scanning electron images (SEM) with synchronous peaks in iodine variability suggest that riverine delivery of terrestrial-derived organo-iodine is the most plausible explanation to account for annual periodicity in the deep-sea coral geochemistry. Whereas previous studies have suggested the presence of annual growth rings in deep-sea corals, this present study provides a mechanism to explain the formation of annual growth bands. Furthermore, deep-sea coral ages based on iodine peak counts agree well with those ages derived from radiocarbon ( 14 C) measurements. These results hold promise for developing chronologies independent of 14 C dating, which is an essential component in constraining reservoir ages and using radiocarbon as a tracer of ocean circulation. Furthermore, the presence of enriched 129 I/ 127 I ratios during the most recent period of skeleton growth is linked to nuclear weapons testing during the 1960s. The sensitivity of the coral skeleton to record changes in surface water 129 I composition provides further evidence that iodine composition and isotope

Uptake and distribution of organo-iodine in deep-sea corals

Science.gov (United States)

Prouty, Nancy G.; Roark, E. Brendan; Mohon, Leslye M.; Chang, Ching-Chih

2018-01-01

Understanding iodine concentration, transport, and bioavailability is essential in evaluating iodine's impact to the environment and its effectiveness as an environmental biogeotracer. While iodine and its radionuclides have proven to be important tracers in geologic and biologic studies, little is known about transport of this element to the deep sea and subsequent uptake in deep-sea coral habitats. Results presented here on deep-sea black coral iodine speciation and iodine isotope variability provides key information on iodine behavior in natural and anthropogenic environments, and its geochemical pathway in the Gulf of Mexico. Organo-iodine is the dominant iodine species in the black corals, demonstrating that binding of iodine to organic matter plays an important role in the transport and transfer of iodine to the deep-sea corals. The identification of growth bands captured in high-resolution scanning electron images (SEM) with synchronous peaks in iodine variability suggest that riverine delivery of terrestrial-derived organo-iodine is the most plausible explanation to account for annual periodicity in the deep-sea coral geochemistry. Whereas previous studies have suggested the presence of annual growth rings in deep-sea corals, this present study provides a mechanism to explain the formation of annual growth bands. Furthermore, deep-sea coral ages based on iodine peak counts agree well with those ages derived from radiocarbon (14C) measurements. These results hold promise for developing chronologies independent of 14C dating, which is an essential component in constraining reservoir ages and using radiocarbon as a tracer of ocean circulation. Furthermore, the presence of enriched 129I/127I ratios during the most recent period of skeleton growth is linked to nuclear weapons testing during the 1960s. The sensitivity of the coral skeleton to record changes in surface water 129I composition provides further evidence that iodine composition and isotope

The 129I hyperfine interaction in fatty acids studied by Moessbauer spectroscopy

International Nuclear Information System (INIS)

Burda, K.; Strzalka, K.; Stanek, J.

1993-01-01

Oleic acid substituted by iodine and saponified by Ca 2+ cations has been studied by 129 I Moessbauer spectroscopy. The quadrupole coupling constants and isomer shifts, determined from the γ-resonance spectra recorded at 4.2 K, have been described by 5p and 5s orbital populations of iodine. It was also found that saponification of the fatty acid has no significant influence on the measured iodine bonds. However, the increased order of fatty acids in soap form is reflected by narrowing of the resonant linewidth due to the reduction of the electric field gradient distribution. (orig.)

Improvements in iodine and ruthenium removal from advanced liquid processing system

Energy Technology Data Exchange (ETDEWEB)

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

2017-09-27

SRNL has considerable experience in designing, engineering, and operating systems for removing iodine-129 (I-129) and ruthenium-106 (Ru-106) from waste streams that are directly analogous to the Advanced Liquid Processing System (ALPS) waste streams. SRNL proposes to provide the technical background and design and engineering support for an improved I-129 and Ru-106 removal system for application to ALPS on the Fukushima Daiichi Nuclear Power Station (NPS).

The distribution and transformations of iodine in the environment

International Nuclear Information System (INIS)

Whitehead, D.C.

1984-01-01

Iodine in the atmosphere is derived largely from seawater. It is probable that the biological production of methyl iodide is important in this transfer. Subsequent photolytic dissociation and oxidation of the methyl iodide, together with other inputs, with partial sorption of the products by aerosols, results in the atmospheric iodine being distributed between various gaseous and particulate forms. Atmospheric iodine is the major source of the iodine in soils, and the process of enrichment continues throughout soil formation and development until ultimately an equilibrium concentration is attained. The atmosphere is also a direct source of iodine for plants, and in some situations may be more important than the soil. Iodine may be lost from soils by leaching, volatilization, and removal in crops. The amounts of iodine reported in groundwaters, and in rivers and lakes remote from human activity, suggest that some leaching of iodine is widespread. Increased amounts of iodine occur in rivers receiving effluent from sewage works. Milk and milk products are now major dietary sources of iodine because their content is often increased by concentrate feedingstuffs supplemented with iodine and/or by the use in dairies of iodophor detergents and sterilants. (author)

Release of iodine radionuclides from gas media in a system of selective block sorbents

International Nuclear Information System (INIS)

Moskvin, L.N.; Miroshnikov, V.S.; Mel'nikov, V.A.; Chetverikov, V.V.

1979-01-01

A scheme of extracting iodine radionuclides from gas flows in a system of selective sorbents has been developed. The method provides separation of three forms of iodine: the aerosol component, the elementary iodine and organic-iodine compounds. Aerosols are trapped by a mechanical filter made of porous polytetrafluoroethylene with pores of no more than 1 μm. Silver-based sorbents for the elementary iodine are made by sintering the granular polytetrafluoroethylene (the size of granules is 0.1-0.5 mm) with of finely dispersed solver (5% mass). Organic iodine compounds are extracted by a silica sorbent impregnated with silver nitrate. The efficiency of sorbents was tested in gas flows with a known content of 131 I in the form of elementary iodine and methyl iodide. The results of experiments show that the efficiency of sorption of elementary iodine by a metallic-silver sorbent and of methyl iodide by a SiO 2 /AgNO 3 sorbent constitutes no less than 99% at a flow rate of up to 200 l/h. The iodine has been extracted at a flow rate of 100 l/h during 100 hours and for that time the efficiency of the iodine sorbtion has not changed. The suggested variant of extracting iodine radionuclides from gaseous media can be used both for fast control of iodine content in gas blowoffs and for researches aimed at studying the distribution of iodine forms in steam-and-gas media depending on nuclear plant operating conditions

Microdosimetry of 129I in the human thyroid

International Nuclear Information System (INIS)

Feige, Y.

1977-01-01

A microdosimetric evaluation of the dose distribution from I-129 in the human thyroid gland, taking into account the various physical, geometrical and physiological parameters suggested by the ICRP Pub. 23 (1975) will be presented, and compared to the dose distribution of other radioisotopes of iodine. Using Dillman's decay scheme data, (NM/MIRD No. 10, p. 73, 1975), and the methods applied by Feige et al. for the microdosimetry of I-125, it is found that the dose to the cell nucleus is about 60% of the 'average' calculated dose for the whole thyroid gland. This follows from the assumptions that typical thyroid follicles are 150 to 300μm in diameter, and that all the iodine is contained in the colloid fraction of the gland. Thus a significant part of the decay energy of I-129, which is due mainly to the beta particles whose average range in tissue is only about 30 μm, is deposited within the colloid itself, and fails to reach the cell nucleus, 3 μm away from the colloid/cell interface. Uncertainties and variations in the parameters of the thyroid model will also be discussed. When thyroid doses due to I-129 releases are assessed, by either the specific activity or the critical pathway models, the conservative environmental and biological assumptions usually made lead to a large margin of safety. If 'average' doses are used instead of the microdosimetric dose distribution an additional safety factor of about 2 is obtained

Gaseous release of radioactive iodine from decaying plants. I. Release following foliar and root uptake

International Nuclear Information System (INIS)

Saas, Arsene; Grauby, Andre

1975-12-01

Iodine uptake by plants is a significant link in the contamination of the food chain. Long half-live iodine was studied considering foliar and root uptake, loss by rain scavenging, residue decay or outgassing in order to assess two aspects of the problem: the importance of outgassing and the effect of the route of transfer on iodine losses. It appeared that iodine release was a function of the vegetal type, there were differences according to the pattern of absorption (via leaf or root) and the processes of iodine release were usually related to biochemical mechanisms [fr

Iodide and iodate sodalites for the long-term storage of iodine-129

International Nuclear Information System (INIS)

Strachan, D.M.; Babad, H.

1979-01-01

There exist several proposals for the storage of 129 I. None of these propose the use of a mineral with demonstrated geologic stability. The work described in this paper has identified the minerals iodide and iodate sodalites [Na 8 (AlSiO 4 ) 6 I 2 /(IO 3 ) 2 ] as good candidates for the long-term storage of 129 I. 4 tables

Iodine deficiency disorders (IDD control in India

Directory of Open Access Journals (Sweden)

Chandrakant S Pandav

2013-01-01

Full Text Available Iodine deficiency disorders (IDD constitute the single largest cause of preventable brain damage worldwide. Majority of consequences of IDD are invisible and irreversible but at the same time these are preventable. In India, the entire population is prone to IDD due to deficiency of iodine in the soil of the subcontinent and consequently the food derived from it. To combat the risk of IDD, salt is fortified with iodine. However, an estimated 350 million people do not consume adequately iodized salt and, therefore, are at risk for IDD. Of the 325 districts surveyed in India so far, 263 are IDD-endemic. The current household level iodized salt coverage in India is 91 per cent with 71 per cent households consuming adequately iodized salt. The IDD control goal in India was to reduce the prevalence of IDD below 10 per cent in the entire country by 2012. What is required is a "mission approach" with greater coordination amongst all stakeholders of IDD control efforts in India. Mainstreaming of IDD control in policy making, devising State specific action plans to control IDD, strict implementation of Food Safety and Standards (FSS Act, 2006, addressing inequities in iodized salt coverage (rural-urban, socio-economic, providing iodized salt in Public Distribution System, strengthening monitoring and evaluation of IDD programme and ensuring sustainability of IDD control activities are essential to achieve sustainable elimination of IDD in India.

Investigation of alumino-phosphate glasses for iodine conditioning

International Nuclear Information System (INIS)

Lemesle, T.

2013-01-01

Iodine 129 is a long-lived intermediate level radioactive waste, which is currently managed by isotopic dilution. In view of an alternative management by geological disposal, we aimed at developing phosphate glasses of the AgI-Ag 2 O-P 2 O 5 -Al 2 O 3 system, elaborated at low temperature and without iodine volatilization. Alumina is expected to induce crosslinking of the phosphate network and thus to improve the thermal and chemical properties. To define a glass composition that meets the specifications, we varied the level of iodine, the Ag 2 O/P 2 O 5 ratio and alumina content. For 1 g.cm -3 of iodine, SEM-EDS observations indicate that alumina solubility is limited to 0.5% mol., independently of Ag 2 O/P 2 O 5 ratio. The structural study by 31 P, 27 Al and 109 Ag MAS NMR, shows that aluminum adopts an octahedral coordination that effectively contributes to the crosslinking of the glassy network and iodine is incorporated without clustering. 31 P- 27 Al NMR correlations confirmed the presence of an alumino-phosphate network, and 31 P- 31 P correlations indicate that iodine does not change the connectivity of the glass network. The glass composition 28,8AgI-44,2Ag 2 O-26,5P 2 O 5 -0,5Al 2 O 3 presents the best compromise between the level of incorporation of iodine and the chemical durability, has a glass transition temperature of 123 C and an initial alteration rate in pure water at 50 C of 6 g.m -2 .d -1 . The long-term behavior of this glass is controlled by a post-alteration structure based on pyrophosphate, which holds nearly 80% of the initial iodine. (author) [fr

Silver iodide reduction in aqueous solution: application to iodine enhanced separation during spent nuclear fuels reprocessing

International Nuclear Information System (INIS)

Badie, Jerome

2002-01-01

Silver iodide is a key-compound in nuclear chemistry either in accidental conditions or during the reprocessing of spent nuclear fuel. In that case, the major part of iodine is released in molecular form into the gaseous phase at the time of dissolution in nitric acid. In French reprocessing plants, iodine is trapped in the dissolver off-gas treatment unit by two successive steps: the first consists in absorption by scrubbing with a caustic soda solution and in the second, residual iodine is removed from the gaseous stream before the stack by chemisorption on mineral porous traps made up of beds of amorphous silica or alumina porous balls impregnated with silver nitrate. Reactions of iodine species with the impregnant are assumed to lead to silver iodide and silver iodate. Enhanced separation policy would make necessary to recover iodine from the filters by silver iodide dissolution during a reducing treatment. After a brief silver-iodine chemical bibliographic review, the possible reagents listed in the literature were studied. The choice has been made to use ascorbic acid and hydroxylamine. An experimental work on silver iodide reduction by this two compounds allowed us to determinate reaction products, stoichiometry and kinetics parameters. Finally, the process has been initiated on stable iodine loaded filters samples. (author) [fr

Prospects of the high power iodine laser

International Nuclear Information System (INIS)

Hohla, K.; Brederlow, G.; Fill, E.; Volk, R.; Witte, K.J.

1976-09-01

The characteristic properties of the iodine laser (gaseous laser substance, photolytic pump mechanism, variable stimulated emission cross-section) made it possible in a relatively short time to generate ns pulses in the kJ range. The Asterix II and III iodine laser systems at IPP are working successfully, and the question arises what prospects are afforded for further iodine laser development. What are the problems that have to be clarified in order to build 10 or 100 kJ systems for laser fusion experiments. According to our experience these can be classified as follows: 1) Short pulse generation and contrast ratio, 2) pulse shaping in a high-gain laser and amplification in the coherent time range, 3) non-linear properties at high intensities, 4) scalable pumping schemes and chemical processes. (orig./WL) [de

Environmental behavior of inorganic anions

International Nuclear Information System (INIS)

Garland, T.R.; Cataldo, D.A.; Fellows, R.J.; Wildung, R.E.

1987-01-01

Recent efforts have addressed two aspects of anion behavior in the soil/plant system. The first involves evaluation of the gaseous component of the terrestrial iodine cycle in soils and plants. Field analyses of 129 I in soils and vegetation adjacent to a fuels reprocessing facility, which was idle for 10 years prior to the study, indicated that there may be a significant gaseous component to the terrestrial iodine cycle. Soil substrates, including a silt-sand, organic forest soil, quartz sand, and a sterilized soil, were amended with radioiodide, and the rates and quality of the volatile components evaluated

Automated sampling and control of gaseous simulations

KAUST Repository

Huang, Ruoguan; Keyser, John

2013-01-01

In this work, we describe a method that automates the sampling and control of gaseous fluid simulations. Several recent approaches have provided techniques for artists to generate high-resolution simulations based on a low-resolution simulation

Partition of iodine (129I and 127I) isotopes in soils and marine sediments

DEFF Research Database (Denmark)

Hansen, Violeta; Roos, Per; Aldahan, Ala

2011-01-01

Natural organic matter, such as humic and fulvic acids and humin, plays a key role in determining the fate and mobility of radioiodine in soil and sediments. The radioisotope 129I is continuously produced and released from nuclear fuel reprocessing plants, and as a biophilic element, its......–60% of the total 129I are associated with organic matter in soil and sediment samples. At a soil/sediment pH below 5.0–5.5, 127I and 129I in the organic fraction associate primarily with the humic acid while at soil/sediment pH > 6 129I was mostly found to be bound to fulvic acid. Anoxic conditions seem...... environmental mobility is strongly linked to organic matter. Due to its long half-life (15.7 million years), 129I builds up in the environment and can be traced since the beginning of the nuclear era in reservoirs such as soils and marine sediments. Nevertheless, partition of the isotope between the different...

Dissociation kinetics of iodine in oxygen-containing electrical discharge plasmas

International Nuclear Information System (INIS)

Zakharov, A.I.; Klopovskii, K.S.; Rakhimova, T.V.; Samorodov, V.A.

1993-01-01

Studies of the kinetics of gaseous media containing oxygen and iodine molecules have been stimulated to a substantial degree by the search for ways of improving iodine-oxygen lasers and by the need for information on loss processes for atmospheric ozone. Results are presented from an experimental study and numerical simulations of the kinetics of the dissociation of iodine in self-sustained volume discharges in high-pressure O 2 :Ar:I 2 mixtures. It is shown that the well-studied mechanism for dissociation based on excitation of iodine molecules in successive collisions with singlet oxygen and excited iodine atoms is supplanted by a substantially different mechanism involving the creation and loss of 10 radicals when the densities of atomic oxygen and ozone are high enough. It is also shown that iodine fractions as low as ∼10 -3 in the mixture lead to rapid loss of ozone molecules while less than 18% of the discharge energy is expended in the production of singlet oxygen

Iodine Isotopes in Precipitation: Temporal Responses to 129I Emissions from the Fukushima Nuclear Accident

DEFF Research Database (Denmark)

Xu, Sheng; Freeman, Stewart P. H. T.; Hou, Xiaolin

2013-01-01

and the behavior of harmful radioiodine in the atmosphere, long-term precipitation samples have been collected over 2010–2012 at Fukushima, Japan for determination of long-lived 129I. It was observed that 129I concentrations of 1.2 × 108 atom/L in 2010 before the accident dramatically increased by ∼4 orders......The Fukushima Dai-ichi Nuclear Power Plant accident in 2011 has released a large amount of radionuclides to the atmosphere, and the radioactive plume has been dispersed to a large area in Europe and returned to Asia. To explore long-term trend of the Fukushima-derived radioactive plume...... environment. A 129I/131I atomic ratio of 16 ± 1 obtained from rainwater samples is comparable with a value estimated for surface soil samples. 129I results from Denmark suggest an insignificant effect of 129I released from Fukushima to the 129I levels in Europe....

Distribution of Iodine-129 in the northwestern North Pacific Ocean between Jan and Feb 2012

International Nuclear Information System (INIS)

Suzuki, Takashi; Otosaka, Shigeyoshi; Kuwabara, Jun

2013-01-01

To evaluate the impact of "1"2"9I from the Fukushima Daiichi Nuclear Power Plant (FNPP) accident, we measured "1"2"9I concentration at three stations: Oyashio-area, transition-area and Kuroshio-area in the northwestern Pacific Ocean. Accident-derived "1"2"9I in surface seawaters was detected at all stations and the highest concentration was observed at the transition-area, 550 km east of the FNPP. The depth profiles show that the accident-derived "1"2"9I was penetrated to 150 m and 200 m depths at the Oyashio-area and transition area, respectively. At the Kuroshio-area, "1"2"9I showed a maximum around 400 - 500 m depth (σ_0=26.0 - 26.2). This is probably due to the isopycnal mixing of surface seawater around 37 N. The highest inventory of accident-derived "1"2"9I was observed at Kuroshio-area. (author)

Iodine generator for reclaimed water purification

Science.gov (United States)

Wynveen, R. A.; Powell, J. D.; Schubert, F. H. (Inventor)

1977-01-01

The system disclosed is for controlling the iodine level in a water supply in a spacecraft. It includes an iodine accumulator which stores crystalline iodine, an electrochemical valve to control the input of iodine to the drinking water and an iodine dispenser. A pump dispenses fluid through the iodine dispenser and an iodine sensor to a potable water tank storage. The iodine sensor electronically detects the iodine level in the water, and through electronic means, produces a correction current control. The correction current control operates the electro-chemical iodine valve to release iodine from the iodine accumulator into the iodine dispenser.

Level and origin of Iodine-129 in the Baltic Sea

Czech Academy of Sciences Publication Activity Database

Hou, XL.; Dahlgaard, H.; Nielsen, SP.; Kučera, Jan

2002-01-01

Roč. 61, č. 3 (2002), s. 331-343 ISSN 0265-931X R&D Projects: GA AV ČR KSK4055109 Keywords : lodine-129 * Baltic sea * neutron activation analysis * seawater Subject RIV: DN - Health Impact of the Environment Quality Impact factor: 0.674, year: 2002

Sequestration of radioactive iodine in silver-palladium phases in commercial spent nuclear fuel

Energy Technology Data Exchange (ETDEWEB)

Buck, Edgar C., E-mail: edgar.buck@pnnl.gov; Mausolf, Edward J.; McNamara, Bruce K.; Soderquist, Chuck Z.; Schwantes, Jon M.

2016-12-15

Radioactive iodine is the Achilles' heel in the design for the safe geological disposal of spent uranium oxide (UO{sub 2}) nuclear fuel. Furthermore, iodine's high volatility and aqueous solubility were mainly responsible for the high early doses released during the accident at Fukushima Daiichi in 2011. Studies Kienzler et al., however, have indicated that the instant release fraction (IRF) of radioiodine ({sup 131/129}I) does not correlate directly with increasing fuel burn-up. In fact, there is a peak in the release of iodine at around 50–60 MW d/kgU, and with increasing burn-up, the IRF of {sup 131/129}I decreases. The reasons for this decrease have not fully been understood. We have performed microscopic analysis of chemically processed high burn-up UO{sub 2} fuel (80 MW d/kgU) and have found recalcitrant nano-particles containing, Pd, Ag, I, and Br, possibly consistent with a high pressure phase of silver iodide in the undissolved residue. It is likely that increased levels of Ag and Pd from {sup 239}Pu fission in high burnup fuels leads to the formation of these metal halides. The occurrence of these phases in UO{sub 2} nuclear fuels may reduce the impact of long-lived {sup 129}I on the repository performance assessment calculations. - Highlights: • A Pd-Ag halide phase has been observed in a high burn-up UO{sub 2} reactor fuel. • The phases contains iodine and bromine. • Iodine release in high burnup fuels may be reduced through the formation of recalcitrant phases.

Glass composite waste forms for iodine confined in bismuth-embedded SBA-15

Energy Technology Data Exchange (ETDEWEB)

Yang, Jae Hwan [Nuclear Fuel Cycle Process Development Division, Korea Atomic Energy Research Institute, 989-111 Daeduk-daero, Yuseong-gu, Daejeon, 305-353 (Korea, Republic of); Department of Nuclear and Quantum Engineering, Korea Advanced Institute of Science and Technology, 291 Daehak-ro, Yuseong-gu, Daejeon, 305-701 (Korea, Republic of); Park, Hwan Seo; Ahn, Do-Hee [Nuclear Fuel Cycle Process Development Division, Korea Atomic Energy Research Institute, 989-111 Daeduk-daero, Yuseong-gu, Daejeon, 305-353 (Korea, Republic of); Yim, Man-Sung, E-mail: msyim@kaist.ac.kr [Department of Nuclear and Quantum Engineering, Korea Advanced Institute of Science and Technology, 291 Daehak-ro, Yuseong-gu, Daejeon, 305-701 (Korea, Republic of)

2016-11-15

The aim of this study was to stabilize bismuth-embedded SBA-15 that captured iodine gas by fabrication of monolithic waste forms. The iodine containing waste was mixed with Bi{sub 2}O{sub 3} (a stabilizing additive) and low-temperature sintering glass followed by pelletizing and the sintering process to produce glass composite materials. Iodine volatility during the sintering process was significantly affected by the ratio of Bi{sub 2}O{sub 3} and the glass composition. It was confirmed that BiI{sub 3}, the main iodine phase within bismuth-embedded SBA-15, was effectively transformed to the mixed phases of Bi{sub 5}O{sub 7}I and BiOI. The initial leaching rates of iodine from the glass composite waste forms ranged 10{sup −3}–10{sup −2} g/m{sup 2} day, showing the stability of the iodine phases encapsulated by the glassy networks. It was also observed that common groundwater anions (e.g., chloride, carbonate, sulfite, and fluoride) elevated the iodine leaching rate by anion exchange reactions. The present results suggest that the glass composite waste form of bismuth-embedded SBA-15 could be a candidate material for stable storage of {sup 129}I. - Highlights: • Glass composite waste forms were developed to stabilize iodine confined in Bi-embedded SBA-15. • BiI{sub 3} within Bi-embedded SBA-15 was transformed to BiOI and Bi{sub 5}O{sub 7}I during sintering process. • Iodine volatility was significantly affected by glass composition and Bi{sub 2}O{sub 3} additive. • Iodine leaching rates were 10{sup −3}–10{sup −2} g/m{sup 2} day due to the stable iodine phases encapsulated by glassy networks. • Glass composite waste form of Bi-embedded SBA-15 is expected to be a candidate material for stable storage of {sup 129}I.

On electrochemical sensor for determining elemental iodine in gas media

International Nuclear Information System (INIS)

Goffman, V.G.; Shajmerdinov, B.U.; Kotelkin, I.M.; Mikhajlova, A.M.; Dobrovol'skij, Yu.A.

1993-01-01

The possibility to use solid electrolyte cells of Ag, AgI/AgI/Au as sensors for determining concentration of element iodine in gaseous media was studied. Independent character of sensor parameters on oxygen content and radiation burden at different humidity was ascertained

Development of a mass spectrometrical isotope dilution analysis for determination of trace iodine levels and its application for food samples

International Nuclear Information System (INIS)

Schindlmeier, W.

1984-01-01

A mass spectrometrical isotope dilution procedure for the determination of trace amounts of iodine in various materials was developed using 129 I as indicator isotope, based on the determination of the 129 I/ 127 I isotope relationship. Negative thermionization was used as ionization method. The analysis procedure, which worked with a standard deviation of between 0,1 and 10% (depending on material tested), was used to determine the iodine level of table salt - both iodized and normal salt (3-6 ppm and less than 0,006 ppm respectively), and food samples with an organic matrix. For comparison the iodine levels were also measured with an iodine-selective electrode. Special preparation and separation procedures were done to suit the sample material. A comparison of the levels of iodine concentration in various powdered milks which were measured by international collaborators using varying methods shows the superior reproducibility of the MS-IDA. (RB) [de

Importance of Microbial Activity On Groundwater Iodate and Organo-Iodine Speciation and Mobility At Two DOE Sites

Energy Technology Data Exchange (ETDEWEB)

Santschi, Peter H. [Texas A & M Univ., College Station, TX (United States); Xu, Chen [Texas A & M Univ., College Station, TX (United States); Schwehr, Kathleen A. [Texas A & M Univ., College Station, TX (United States); Kaplan, Daniel I. [Savannah River Site (SRS), Aiken, SC (United States). Savannah River National Lab. (SRNL); Yeager, Chris M. [Savannah River Site (SRS), Aiken, SC (United States). Savannah River National Lab. (SRNL)

2016-03-01

Iodine (I) occurs in multiple oxidation states in aquatic systems in the form of organic and inorganic species (iodide and iodate). This fact leads to complex biogeochemical cycling of Iodine and its long-lived isotope, ¹²⁹I, a major by-product of nuclear fission. Results from our newly developed, sensitive and rapid method for speciated isotopic ratios (¹²⁹I/¹²⁷I) via GC-MS, which compare favorably with Accelerator Mass Spectroscopy, demonstrate that the mobility of ¹²⁹I species greatly depends on the type of I species and its concentration, pH, and sediment redox state. At ambient concentrations (~10⁷ M), I- and IO^-3 are significantly retarded by sorption to mineral surfaces and covalent binding to aromatic moieties in natural organic matter (NOM), even when NOM is present at low concentrations such as occur at Hanford. At concentrations traditionally examined in sorption studies (≥ 10^-4 M), I- travels along with the water. Iodate removal can also occur through incorporation into CaCO₃ crystal lattice, e.g., at the Hanford Site. Removal of iodine from the groundwater through interaction with NOM is complicated by the release of mobile organo-I species, as was observed at SRS and Hanford. A small fraction of NOM that is bound to iodine can behave as a mobile organo-I source, a process that we were able to numerically simulate. Field and laboratory studies evaluating the cause for steady increases in ¹²⁹I concentrations (up to 1000 pCi L-1) emanating from radiological basins at SRS indicate that an increase of 0.7 pH units in groundwater over 17 years can account for the observed increased groundwater ¹²⁹I concentrations. Bacteria from a ¹²⁹I-contaminated aerobic aquifer at the F-area of SRS can accumulate I- at environmentally relevant concentrations (10^-7 M), and enzymatically oxidize I-, which together with microbially produced Mn

Investigations concerning the exchange of iodine from non-volatile organic iodine compounds

International Nuclear Information System (INIS)

Psarros, N.; Duschner, H.; Molzahn, D.; Schmidt, L.; Heise, S.; Jungclas, H.; Brandt, R.; Patzelt, P.

1990-10-01

The iodine produced by nuclear fission is removed during the reprocessing of exhausted nuclear fuel elements by desorption achieving good decontamination factors. Nevertheless the further optimization of the process requires detailed information about the iodine speciation during fuel reprocessing, and about possible reactions. For the study of decomposition reactions of iodo-alcanes, which are built up during the fuel recycling process, we developed a method for the synthesis of labelled iodo-dodecane, which was used as tracer. In order to identify the iodo species in the organic phase of the reprocessing cycle we applied plasma desorption time-of-flight mass spectroscopy. The problem of the volatility of the iodo-compounds in the ultra vacuum of the mass spectrometer was overcome by derivatization of the iodo-alcanes with dithizon, which yielded non-volatile ionic alcyltetrazolium iodides. Beta-spectrometric analysis of the exhaust condensates collected from the organic phase of the WAK reprocessing cycle revealed beside iodine-129 the existence of a low-energetic beta emitter, which has yet to be identified. A literature survey on the topic was also performed. (orig.) With 42 refs., 9 figs [de

Dry deposition of gaseous radioiodine and particulate radiocaesium onto leafy vegetables

International Nuclear Information System (INIS)

Tschiersch, Jochen; Shinonaga, Taeko; Heuberger, Heidi

2009-01-01

Radionuclides released to the atmosphere during dry weather (e.g. after a nuclear accident) may contaminate vegetable foods and cause exposure to humans via the food chain. To obtain experimental data for an appropriate assessment of this exposure path, dry deposition of radionuclides to leafy vegetables was studied under homogeneous and controlled greenhouse conditions. Gaseous 131 I-tracer in predominant elemental form and particulate 134 Cs-tracer at about 1 μm diameter were used to identify susceptible vegetable species with regard to contamination by these radionuclides. The persistence was examined by washing the harvested product with water. The vegetables tested were spinach (Spinacia oleracea), butterhead lettuce (Lactuca sativa var. capitata), endive (Cichorium endivia), leaf lettuce (Lactuca sativa var. crispa), curly kale (Brassica oleracea convar. acephala) and white cabbage (Brassica oleracea convar. capitata). The variation of radionuclides deposited onto each vegetable was evaluated statistically using the non-parametric Kruskal-Wallis Test and the U-test of Mann-Whitney. Significant differences in deposited 131 I and 134 Cs activity concentration were found among the vegetable species. For 131 I, the deposition velocity to spinach normalized to the biomass of the vegetation was 0.5-0.9 cm 3 g -1 s -1 which was the highest among all species. The particulate 134 Cs deposition velocity of 0.09 cm 3 g -1 s -1 was the highest for curly kale, which has rough and structured leaves. The lowest deposition velocity was onto white cabbage: 0.02 cm 3 g -1 s -1 (iodine) and 0.003 cm 3 g -1 s -1 (caesium). For all species, the gaseous iodine deposition was significantly higher compared to the particulate caesium deposition. The deposition depends on the sensitive parameters leaf area, stomatal aperture, and plant morphology. Decontamination by washing with water was very limited for iodine but up to a factor of two for caesium.

Molecular structures and thermodynamic properties of monohydrated gaseous iodine compounds: Modelling for severe accident simulation

Science.gov (United States)

Sudolská, Mária; Cantrel, Laurent; Budzák, Šimon; Černušák, Ivan

2014-03-01

Monohydrated complexes of iodine species (I, I2, HI, and HOI) have been studied by correlated ab initio calculations. The standard enthalpies of formation, Gibbs free energy and the temperature dependence of the heat capacities at constant pressure were calculated. The values obtained have been implemented in ASTEC nuclear accident simulation software to check the thermodynamic stability of hydrated iodine compounds in the reactor coolant system and in the nuclear containment building of a pressurised water reactor during a severe accident. It can be concluded that iodine complexes are thermodynamically unstable by means of positive Gibbs free energies and would be represented by trace level concentrations in severe accident conditions; thus it is well justified to only consider pure iodine species and not hydrated forms.

Review of microfluidic cell culture devices for the control of gaseous microenvironments in vitro

Science.gov (United States)

Wu, H.-M.; Lee, T.-A.; Ko, P.-L.; Chiang, H.-J.; Peng, C.-C.; Tung, Y.-C.

2018-04-01

Gaseous microenvironments play important roles in various biological activities in vivo. However, it is challenging to precisely control gaseous microenvironments in vitro for cell culture due to the high diffusivity nature of gases. In recent years, microfluidics has paved the way for the development of new types of cell culture devices capable of manipulating cellular microenvironments, and provides a powerful tool for in vitro cell studies. This paper reviews recent developments of microfluidic cell culture devices for the control of gaseous microenvironments, and discusses the advantages and limitations of current devices. We conclude with suggestions for the future development of microfluidic cell culture devices for the control of gaseous microenvironments.

A summary of global 129I in marine waters

International Nuclear Information System (INIS)

He Peng; Aldahan, A.; Possnert, G.; Hou, X.L.

2013-01-01

Despite the many investigations concerning the occurrence of anthropogenic iodine-129 in the atmosphere, terrestrial and marine environments, there is a lack of a comprehensive collection of data on the distribution of the isotope in marine waters. The temporal and spatial variability of anthropogenic 129 I is strongly linked to the major point sources in the Irish Sea and the English Channel and the global marine spreading pathways are partly outlined from these sources. The temporal evolution is still, however, not well defined when transport and dissipation are considered in the different oceans and ocean compartments. We here summarize available published literature data on 129 I temporal and spatial distribution in the global marine water. The results show presence of numerous data sets for the North Atlantic and Arctic Oceans where strong variability in terms of water depth, time and location also occur. Scarcity of data on 129 I from the Pacific, Indian and South Atlantic Oceans demonstrates gaps in the coverage of the isotope spatial extent. These shortcomings in the spatial coverage may relate to the understanding that the anthropogenic 129 I signal will take a long time to be transported, if at all, from the North Atlantic into other oceans. Data from recent expeditions in the Southern oceans and the Geotraces ocean profiling will reveal additional information about 129 I distribution in the marine waters.

Iodination of phenol

International Nuclear Information System (INIS)

Christiansen, J.V.; Feldthus, A.; Carlsen, L.

1990-01-01

Phenol is iodinated in aqueous solution at pH 5 (acetate buffer) by elemental iodine or, if the iodine is present as iodide, enzymatically controlled by peroxidases. Generally mono-, di- and triiodophenols are obtained, the overall product composition being virtually identical for the two iodination modes. However, there is a tendency to a higher para to ortho ratio for the enzymatically controlled reaction. The mutual ratios of the single iodophenols depends on the initial concentration ratio between phenol and the iodinating species. The first step in the iodination leads preferentially to substitution in the ortho position rather than in the para position in contract to e.g. the corresponding bromination. The relative rates of the competive reactions in the combined iodination scheme has been derived. (author) 2 tabs., 3 ills., 15 refs

Study of molecular iodine-epoxy paint mass transfer

Energy Technology Data Exchange (ETDEWEB)

Belval-Haltier, E [Inst. de Protection et Surete Nucleaire, IPSN, CEN Cadarache, St. Paul-lez-Durance (France)

1996-12-01

The mass transfer phenomena may have a significant influence on the quantity of I{sub 2} which could be released following a severe accident of a nuclear power plant and specially the mass transfer of iodine onto containment surfaces. So, the objective of the present work was to evaluate which phase limited the adsorption process of iodine onto gaseous epoxy paint under a range of conditions which may be relevant to a severe reactor accident. In this aim, a series of experiments was conducted in which the sorption kinetics of molecular iodine, labelled with {sup 131}I, was measured by monitoring continuously the accumulation of this species on the epoxy surface. For each test condition, the initial deposition velocity was determined and the corresponding gas phase mass transfer, kg, was estimated by using the heat transfer analogy for a laminar flow passing over a flat plate. Then, the surface reaction rate, Kr, was deduced from these two values. Experiments performed indicated that iodine adsorption onto epoxy paint is highly dependent on temperature, relative humidity of the carrier gas and moisture content of the painted coupon. In dry air flow conditions, the adsorption of iodine onto paint was found to increase with temperature and to be limited by the surface reaction rate, Kr. The I{sub 2} adsorption rate was found to increase with the humidity of carrier gas and in some studied conditions, the initial deposition velocity appeared to be controlled by gas phase mass transfer rather than surface interaction. The same phenomenon has been observed with an increase of the initial water content of the painted coupon. (author) 6 figs., 1 tab., 8 refs.

Speciation Analysis and Environmental Tracer Studies of ¹²⁹I

DEFF Research Database (Denmark)

Zhang, Luyuan

, Japan were investigated. Iodate for both 129I and 127I is the predominant form for the seawater in the central Arctic and Greenland coast, whereas iodide is the major specie of 129I and 127I in Danish coast. A distinct distribution pattern of iodine species was observed in Fukushima offshore seawater......, such as the Greenland Sea, and the western Atlantic Ocean, as well as to the atmosphere and the Arctic ecosystem. Aerosol samples collected at two locations (Risø, Denmark, a coastal site, and Tsukuba Japan, about 170 km southwest of the Fukushima Dai-ichi nuclear power plant) during spring 2011 (shortly after...... in real samples demonstrate that the developed method is reliable for accurate determination of 129I and 127I species in aerosol samples. Distributions of chemical species (iodide and iodate) of 129I and 127I in the seawater from the central Arctic, Greenland coast, Danish coast and offshore Fukushima...

Uranium enrichment export control guide: Gaseous diffusion

Energy Technology Data Exchange (ETDEWEB)

1989-09-01

This document was prepared to serve as a guide for export control officials in their interpretation, understanding, and implementation of export laws that relate to the Zangger International Trigger List for gaseous diffusion uranium enrichment process components, equipment, and materials. Particular emphasis is focused on items that are especially designed or prepared since export controls are required for these by States that are party to the International Nuclear Nonproliferation Treaty.

Balance and behavior of gaseous radionuclides released during initial PWR fuel reprocessing operations

International Nuclear Information System (INIS)

Leudet, A.; Miquel, P.; Goumondy, P.J.; Charrier, G.

1982-08-01

Five fuel pins, taken from a PWR fuel assembly with 32000 MWD/t burn-up were chopped and dissolved in leak-proof equipment designed for accurate determination of the composition and quantity of gaseous elements released in these operations. Analytical methods were specially developped to determine directly the noble gases, tritium and gaseous carbon compounds in the gas phase. Volatile iodine was kept as close as possible to the source by cold traps, then transferred to a caustic solution for quantitative analysis. The quantities and activities of gaseous fission products thus determined were compared with predicted values obtained through computation. Very good agreement was generally observed

Balance and behavior of gaseous radionuclides released during initial PWR fuel reprocessing operations

International Nuclear Information System (INIS)

Leudet, A.; Miquel, P.; Goumondy, P.J.; Charrier, G.

1983-01-01

Five fuel pins, taken from a PWR fuel assembly with 32,000 MwD/t burn-up were chopped and dissolved in leak-proof equipment designed for accurate determination of the composition and quantity of gaseous elements released in these operations. Analytical methods were specially developed to determine directly the noble gases, tritium and gaseous carbon compounds in the gas phase. Volatile iodine was kept as close as possible to the source by cold traps, then transferred to a caustic solution for quantitative analysis. The quantities and activities of gaseous fission products thus determined were compared with predicted values obtained through computation. Very good agreement was generally observed

Field measurements of the washout coefficient for gaseous iodine likely to be released on accidental conditions

International Nuclear Information System (INIS)

Caput, C.; Camus, H.; Gauthier, D.; Belot, Y.

1992-01-01

Field experiments were performed in Brittany to assess the washout coefficient Λ for molecular iodine. During each run, a few grams of nonradioactive iodine were released from a 12 meters telescopic mast, and the rain was sampled at a short distance downwind along complete transversal sections of the plume. The amount of iodine in each sample was determined by ionic chromatography to calculate the washout coefficient. In most cases, the results obtained (a few 10 -5 s -1 ) are not so different as expected from the theoretical values assuming a complete solubility of iodine in rain water. 4 refs., 1 fig., 1 tab

Adsorption and revaporisation studies on iodine oxide aerosols deposited on containment surface materials in LWR

International Nuclear Information System (INIS)

Tietze, S.; Foreman, M.R.StJ.; Ekberg, C.; Kaerkelae, T.; Auvinen, A.; Tapper, U.; Lamminmaeki, S.; Jokiniemi, J.

2012-12-01

During a hypothetical severe nuclear accident, the radiation field will be very high in the nuclear reactor containment building. As a result gaseous radiolysis products will be formed. Elemental iodine can react in the gaseous phase with ozone to form solid iodine oxide aerosol particles (iodine oxide). Within the AIAS (Adsorption of Iodine oxide Aerosols on Surfaces) project the interactions of iodine oxide (IOx) aerosols with common containment surface materials were investigated. Common surface materials in Swedish and Finnish LWRs are Teknopox Aqua V A paint films and metal surfaces such as Cu, Zn, Al and SS, as well as Pt and Pd surfaces from hydrogen recombiners. Non-radioactive and 131 I labelled iodine oxide aerosols were produced with the EXSI CONT facility from elemental iodine and ozone at VTT Technical Research Centre of Finland. The iodine oxide deposits were analysed with microscopic and spectroscopic measurement techniques to identify the kind of iodine oxide formed and if a chemical conversion on the different surface materials occurs. The revaporisation behaviour of the deposited iodine oxide aerosol particles from the different surface materials was studied under the influence of heat, humidity and gamma irradiation at Chalmers University of Technology, Sweden. Studies on the effects of humidity were performed using the FOMICAG facility, while heat and irradiation experiments were performed in a thermostated heating block and with a gammacell 22 having a dose rate of 14 kGy/h. The revaporisation losses were measured using a HPGe detector. The revaporisated 131 I species from the surfaces were chemically tested for elemental iodine formation. The parameter dominating the degradation of the produced iodine oxide aerosols was humidity. Cu and Zn surfaces were found to react with iodine from the iodine oxide aerosols to form iodides, while no metal iodides were detected for Al and SS samples. Most of the iodine oxide aerosols are assumed to be

Gaseous poison injection device

International Nuclear Information System (INIS)

Kubota, Ryuji; Sugisaki, Toshihiko; Inada, Ikuo.

1983-01-01

Purpose: To rapidly control the chain reaction due to thermal neutrons in a reactor core by using gaseous poisons as back-up means for control rod drives. Constitution: Gaseous poisons having a large neutron absorption cross section are used as back-up means for control rod drives. Upon failure of control rod insertion, the gaseous poisons are injected into the lower portion of the reactor core to control the reactor power. As the gaseous poisons, vapors at a high temperature and a higher pressure than that of the coolants in the reactor core are injected to control the reactor power due to the void effects. Since the gaseous poisons thus employed rapidly reach the reactor core and form gas bubbles therein, the deccelerating effect of the thermal neutrons is decreased to reduce the chain reaction. (Moriyama, K.)

Dither Cavity Length Controller with Iodine Locking

Directory of Open Access Journals (Sweden)

Lawson Marty

2016-01-01

Full Text Available A cavity length controller for a seeded Q-switched frequency doubled Nd:YAG laser is constructed. The cavity length controller uses a piezo-mirror dither voltage to find the optimum length for the seeded cavity. The piezo-mirror dither also dithers the optical frequency of the output pulse. [1]. This dither in optical frequency is then used to lock to an Iodine absorption line.

Head-end iodine removal from a reprocessing plant with a solid sorbent

International Nuclear Information System (INIS)

Wilhelm, J.G.; Furrer, J.; Schultes, E.

1976-01-01

In the first large-scale reprocessing plant planned in the Federal Republic of Germany a total amount of 580 kg of iodine per annum will be released in the fuel dissolution process for a maximum heavy metal throughput of 1800 tons per year and 40,000 MWd/t of burnup. The main portion of the iodine is formed by the 129 I (T/sub 1/2/ = 1.6 x 10 7 a) isotope of which 82 Ci at the maximum are released every year. With the scheduled fuel element storage time of greater than or equal to 220 d the simultaneous release of 131 I is less than or equal to 12.5 Ci the mass of which does not play any part. According to the computer model presently imposed in the Federal Republic of Germany for treatment of the environmental impact by radioiodine, a total decontamination factor of 340 must be attained. This implies a long-term diffusion factor of 1 x 10 -7 s/m 3 for releases via the stack of the reprocessing plant and a limit value of 50 mrem/a at the maximum for the thyroid dose to the critical group of the population via the ingestion path. The flowsheet for dissolver off-gas cleaning in a reprocessing plant employing solid iodine sorption material and the arrangement of filter components are discussed. The principle of an iodine sorption filter is described which allows exhaustive loading of the iodine sorption material. The removal reactions of different organic iodine compounds and the loading capacity and removal efficiency of the iodine sorption material in the original dissolver off-gases of reprocessing plants are indicated. Studies on the influence of filter poisons are reported.Operating experience gathered with a first iodine sorption filter in operation is discussed; this filter has been used to remove practically all iodine produced in the dissolver off-gas of the Karlsruhe Reprocessing Pilot Plant (WAK). Direct measurement of 129 I in samples of filter material using a low energy photon spectrometer is briefly reported

Microbial influences on the mobility and transformation of radioactive iodine in the environment

International Nuclear Information System (INIS)

Amachi, Seigo; Fujii, Takaaki; Shinoyama, Hirofumi; Muramatsu, Yasuyuki

2005-01-01

Long-lived radioactive iodine ( 129 I, half-life: 1.57x10 7 y) has been released into the environment from nuclear fuel reprocessing plants. 129 I may also be released from ground storage of nuclear waste. Given its long half-life, a better understanding of the behavior of iodine in the environment is necessary to ensure the safety of humans and the health of the environment. In this report, we summarize our recent results and new experimental data about microbial influences on the mobility and transformation of iodine. Microbial volatilization of organic iodine was observed in soil slurries and seawater samples, and various species of aerobic bacteria were considered to play a significant role through methylation of iodide (I - ) to form methyl iodide (CH 3 I). The volatilization of iodine was also found in iodide-rich natural gas brine water, where iodide concentration is approximately 2,000 times higher than that in seawater. In this case, however, a significant amount of molecular iodine (I 2 ) was produced together with organic iodine compounds. Iodide-oxidizing bacteria, which oxidize iodide to I 2 , were isolated from seawater and natural gas brine water. Phylogenetically, they were divided into two groups within the alpha-subclass of the Proteobacteria (Roseovarius sp. and unidentified bacteria), and they produced not only I 2 but also diiodomethane (CH 2 I 2 ) and chloroiodomethane (CH 2 CII). Iodide-accumulating bacteria, which accumulate iodide to concentrations 5,500-fold over that of the medium, were also isolated from marine sediment. They were closely related to Arenibacter troitsensis, and iodide uptake was medicated by an active transport system. Our results suggest that the fate of iodine can be affected by microorganisms, particularly by bacteria, through processes such as volatilization, oxidation, and accumulation. (author)

Experimental study of iodine removal efficiency in self-priming venturi scrubber

International Nuclear Information System (INIS)

Gulhane, N.P.; Landge, A.D.; Shukla, D.S.; Kale, S.S.

2015-01-01

Highlights: • Fabrication, erection of experimental set up and carrying out experimentation with self priming venturi scrubber. • Predicting solubility of iodine in water and its pH dependency. • Increasing pH of water increases iodine removal efficiency. • Maximum iodine removal efficiency is obtained at 10 pH of water using sodium thiosulphate. - Abstract: The objective of present experimental study is to examine the iodine removal efficiency of a self-priming venturi scrubber for submerged operating condition. The venturi scrubber is used in Containment Filtered Venting System of nuclear power plants to remove the gaseous pollutants from contaminated gas during severe accidents. The experiment consists of mixing the iodine vapours with the air using suction venturi and pressure cooker system. The purpose of iodine mixing with air is to examine scrubbing performance of the designed venturi scrubber with water as scrubbing liquid. The performance parameters of venturi scrubber are expressed mainly in terms of pressure drop and iodine removal efficiency. The iodine removal efficiency of venturi scrubber is estimated for a series of two experiments by measuring the quantity of iodine in water from iodometric titration with four distinct pH of water. It has been experimentally observed that iodine removal efficiency is improved by using higher pH value of scrubbing liquid since solubility of iodine gets improved at higher pH

Elimination of interference of 129-iodine by its adsorption at extraction separation of 99-technetium

International Nuclear Information System (INIS)

Metelkova, M.; Tkac, P.; Kopunec, R.

2001-01-01

Three types of macro-amount of anions SO 4 2- , CO 3 2- , OH - in the presence of I- were chosen in this work for comparison of competition with TcO 4 - anions in extraction reaction with Ph 4 As + , where weak, medium and strong competition can be expected respectively. Ph 4 AsCl in chloroform was used as organic phase. The influence of solid AgI or AgCl on Tc extraction was also studied in this extraction systems. The extraction of technetium after four-multiplied extraction from chosen solutions was studied. This procedure was applied in the process of Tc extraction from solutions of reprocessing plant. Various concentrations of K 2 CrO 4 and UO 2 (NO 3 ) 2 in water phase on Tc extraction was investigate, too. The influence of I - ( 131 I) in the process of extraction separation of technetium was studied. The iodine removal was taken out from the solution by its adsorption on insoluble AgI or AgCl phase. The yields for 99m Tc were higher than 95% in organic phase and for 131 I higher than 80% in AgI or AgCl. It is possible to note, that this procedure can be also applied for 99 Tc and 129 I separation and estimation. The results of the extraction are presented in the form of graphical plots of technetium distribution ratio (D Tc , log D Tc ) or extraction yield (E Tc %) against concentration of investigate component in aqueous phase. (authors)

Abiotic production of iodine molecules in irradiated ice

Science.gov (United States)

Choi, Wonyong; Kim, Kitae; Yabushita, Akihiro

2015-04-01

Reactive halogen species play an important role in Earth's environmental systems. Iodine compounds are related to ozone depletion event (ODE) during Antarctic spring, formation of CCN (cloud condensation nuclei), and controlling the atmospheric oxidizing capacity. However, the processes and mechanisms for abiotic formation of iodine compounds in polar region are still unclear. Although the chemical reactions taking place in ice are greatly different from those in aquatic environment, reaction processes of halogens in frozen condition have rarely studied compared to those in water. In this study, we investigated iodide oxidation to form triiodide (I3-) in ice phase under UV irradiation ( λ > 300 nm) and dark condition. The production of I3- through iodide oxidation, which is negligible in aqueous solution, was significantly accelerated in ice phase even in the absence of UV irradiation. The following release of gaseous iodine molecule (I2) to the atmosphere was also monitored by cavity ring-down spectroscopy (CRDS). We speculate that the markedly enhanced iodide oxidation in polycrystalline ice is due to the freeze concentration of iodides, protons, and dissolved oxygen in the ice crystal grain boundaries. The experiments conducted under ambient solar radiation of the Antarctic region (King George Island, 62°13'S 58°47'W, sea level) also confirmed that the generation of I3- via iodide oxidation process is enhanced when iodide is trapped in ice. The observed intrinsic oxidative transformation of iodide to generate I3-(aq) and I2(g) in frozen environment suggests a previously unknown pathway for the substantial release of reactive iodine species to the atmosphere.

Guidelines on the use of stable iodine as a prophylactic measure during nuclear emergencies

International Nuclear Information System (INIS)

1995-09-01

Among the fission products that may be released in a power reactor accident the radio iodines are unique in that the dose received by persons exposed by inhalation of radio iodines in the gaseous plume may be substantially reduced. GMA-9 provides guidance on the medical aspects of the use of stable iodine compounds as a prophylactic measure in the event of a nuclear accident. A review of the physiologic basis for the use of stable iodine as a prophylactic measure and the effects of radiation on the thyroid gland are provided. Logistic factors that must be considered to provide the optimum level of radiological protection and medical safety are also addressed. 71 refs., 6 tabs., 2 figs

Guidelines on the use of stable iodine as a prophylactic measure during nuclear emergencies

Energy Technology Data Exchange (ETDEWEB)

NONE

1995-09-01

Among the fission products that may be released in a power reactor accident the radio iodines are unique in that the dose received by persons exposed by inhalation of radio iodines in the gaseous plume may be substantially reduced. GMA-9 provides guidance on the medical aspects of the use of stable iodine compounds as a prophylactic measure in the event of a nuclear accident. A review of the physiologic basis for the use of stable iodine as a prophylactic measure and the effects of radiation on the thyroid gland are provided. Logistic factors that must be considered to provide the optimum level of radiological protection and medical safety are also addressed. 71 refs., 6 tabs., 2 figs.

Iodine-129 in the environment of a nuclear fuel reprocessing plant: Pt. 5

International Nuclear Information System (INIS)

Hauschild, J.; Aumann, D.C.

1989-01-01

A field investigation of the transfer of 129 I and of natural 127 I in the soil-pasture-cow-milk/meat pathway has been carried out at a dairy farm situated 5400 m to the north of the small Karlsruhe nuclear fuel reprocessing plant. Soil and herbage samples were collected during the period between April 1986 and April 1987. Milk samples were collected during the 1986 grazing season. The concentrations of 129 I and 127 I were determined in all soil, herbage and milk samples. (author)

Production of gaseous radiotracers CH3I and I2 through Na123I salt

International Nuclear Information System (INIS)

Candeiro, R.E.M.; Pereira, W.P.

2011-01-01

The objective of the present work was to develop, separately, methodology for production of two gaseous tracers through the sodium iodide NaI marked with 123 I. Found in the nature in form different, the iodine has been used in diverse works in the area of the industry and health. These two forms of the gaseous iodine, the methyl iodide, CH 3 I, and molecular iodine, I 2 , are very unstable and volatile in the ambient temperature and presents different problems in clean-up and monitoring systems. The syntheses were processed with sodium iodide (NaI) 1M aqueous solution marked with 1 23I . The production of gas I 2 was realized with in chlorine acid (HCl) and sodium iodate salt (NaIO 3 ) and the CH 3 I was used, the salt of NaI and the reagent (CH 3 ) 2 SO 4 . The production of gases was initially realized through in unit in glass with an inert material and the purpose was to study the kinetic of reaction and to determine the efficiency of production. The two synthesis occurs in the reaction bottle and after of produced, the gas is stored in the collect bottle that contains a starch solution for fixed the I 2 , and in syntheses of CH 3 I contains a silver nitrate solution for your fixation. To determine the efficiency of production of gases, analytic tests were realized, where the consumption of iodide ions of the bottle of reaction are measured. The optimization of production of the each gaseous tracer was studied varying parameter as: concentration of iodide, concentration of acid and temperature. After, the syntheses of the radiotracers were realized in the compact unit, having been used as main reagent the salt radiated of sodium iodide, Na 123 I. The transportation of elementary iodine and methyl iodine was studied by a scintillation detector NaI (2 x 2)' positioned in the reaction bottle. (author)

RAIM-A model for iodine behavior in containment under severe accident condition

Energy Technology Data Exchange (ETDEWEB)

Kim, Han Chul; Cho, Yeong Hun [Korea Institute of Nuclear Safety, Daejeon (Korea, Republic of)

2015-12-15

Following a severe accident in a nuclear power plant, iodine is a major contributor to the potential health risks for the public. Because the amount of iodine released largely depends on its volatility, iodine's behavior in containment has been extensively studied in international programs such as International Source Term Programme-Experimental Program on Iodine Chemistry under Radiation (EPICUR), Organization for Economic Co-operation and Development (OECD)-Behaviour of Iodine Project, and OECD-Source Term Evaluation and Mitigation. Korea Institute of Nuclear Safety (KINS) has joined these programs and is developing a simplified, stand-alone iodine chemistry model, RAIM (Radio-Active Iodine chemistry Model), based on the IMOD methodology and other previous studies. This model deals with chemical reactions associated with the formation and destruction of iodine species and surface reactions in the containment atmosphere and the sump in a simple manner. RAIM was applied to a simulation of four EPICUR tests and one Radioiodine Test Facility test, which were carried out in aqueous or gaseous phases. After analysis, the results show a trend of underestimation of organic and molecular iodine for the gas-phase experiments, the opposite of that for the aqueous-phase ones, whereas the total amount of volatile iodine species agrees well between the experiment and the analysis result.

Kinetic cartography of radioisotopes of iodine in the thyroid follicles of the new-born rats under low or standard iodine diet: Analyzed using Secondary Ion Mass Spectrometry (NanoSIMS50): Contribution to the study of the consequences of Chernobyl; Cartographie cinetique des radioisotopes de l'iode dans le follicule thyroidien du rat nouveau-ne carence en iode ou non. Analyse par spectrometrie de masse d'ions secondaires (NanoSIMS50). Contribution a l'etude des consequences de Tchernobyl

Energy Technology Data Exchange (ETDEWEB)

Elbast, M

2008-03-15

The most significant impact of the Chernobylsk accident is the increased incidence of thyroid cancers among children in contaminated areas. To estimate the radiation dose provided by radioiodine released after Chernobylsk (iodine 131 and short-lived isotopes, iodine 132, 133, 134, 135), we used new-born rats to mimic the situation of fallout contamination (young age and iodine deficiency). The pups, under low iodine diet and under standard diet, were contaminated with {sup 129}I at ages varying between 2 to 15 days and sacrificed 1, 4, 8, 24 hours and 4, 8 days after contamination. The variation in intra colloidal iodine distribution from 1 hour to 8 days was performed using a new ionic nano probe (NanoSIMS50). This method permits to discriminate between the newly incorporated iodine (129) and the initial pool of iodine (127). SIMS observations permit to heterogeneous intra and inter follicular distribution of {sup 129}I. Iodine deficiency increases the absorbed amounts of iodine by a factor 10. Dosimetric estimations show an important contribution of short-lived radioiodine to the total thyrocyte dose. In conclusion, we have demonstrated that the age and the iodine deficiency accelerate the absorption of iodine in follicles and that the contribution of short-lived iodine connate ne neglected. (author)

Studies of iodine concentration in steel and transition metals

International Nuclear Information System (INIS)

Kormann, C.; Kozlowski, W.; Oleksi-Frenzel, J.; Nachtigall, K.; Neste, A. van; Welsh, M.; Titze-Zaeske, B.; Plieth, W.

1990-01-01

Radioactive iodine which originates from nuclear fuel reprocessing plants as a fission product and consists mainly of the radioactive isotopes 129 I, 131 I, and of the inactive 127 I, must be quantitatively adsorbed at the end of the process for the purpose of safe waste disposal. Inspite of using high-alloy austenitic chrome nickel steels, major corrosion effects were observed at tubes and containers of the PASSAT dissolver waste gas purifier. This research project serves to clarify the question in which parts of the installation iodine concentration is to be expected under certain conditions. Furthermore it serves to identify the redox state of iodine in the various installation components. For this purpose steel (1.4306esu and 1.4563N), zirconium and titanium were studied in nitric iodic media. With the objective of calculating iodine adsorption isotherms, the following methods were used to obtain qualitative and quantitative data: FTIR, ellipsometry, 131 I radiotracer method, cyclo-voltametry, closed circuit potential measurements, ion chromatography. (orig./DG) [de

Active molecular iodine photochemistry in the Arctic.

Science.gov (United States)

Raso, Angela R W; Custard, Kyle D; May, Nathaniel W; Tanner, David; Newburn, Matt K; Walker, Lawrence; Moore, Ronald J; Huey, L G; Alexander, Liz; Shepson, Paul B; Pratt, Kerri A

2017-09-19

During springtime, the Arctic atmospheric boundary layer undergoes frequent rapid depletions in ozone and gaseous elemental mercury due to reactions with halogen atoms, influencing atmospheric composition and pollutant fate. Although bromine chemistry has been shown to initiate ozone depletion events, and it has long been hypothesized that iodine chemistry may contribute, no previous measurements of molecular iodine (I 2 ) have been reported in the Arctic. Iodine chemistry also contributes to atmospheric new particle formation and therefore cloud properties and radiative forcing. Here we present Arctic atmospheric I 2 and snowpack iodide (I - ) measurements, which were conducted near Utqiaġvik, AK, in February 2014. Using chemical ionization mass spectrometry, I 2 was observed in the atmosphere at mole ratios of 0.3-1.0 ppt, and in the snowpack interstitial air at mole ratios up to 22 ppt under natural sunlit conditions and up to 35 ppt when the snowpack surface was artificially irradiated, suggesting a photochemical production mechanism. Further, snow meltwater I - measurements showed enrichments of up to ∼1,900 times above the seawater ratio of I - /Na + , consistent with iodine activation and recycling. Modeling shows that observed I 2 levels are able to significantly increase ozone depletion rates, while also producing iodine monoxide (IO) at levels recently observed in the Arctic. These results emphasize the significance of iodine chemistry and the role of snowpack photochemistry in Arctic atmospheric composition, and imply that I 2 is likely a dominant source of iodine atoms in the Arctic.

Active molecular iodine photochemistry in the Arctic

Energy Technology Data Exchange (ETDEWEB)

Raso, Angela R.; Custard, Kyle D.; May, Nathaniel W.; Tanner, David; Newburn, Matthew K.; Walker, Lawrence R.; Moore, Ronald J.; Huey, L. G.; Alexander, Lizabeth; Shepson, Paul B.; Pratt, Kerri A.

2017-09-05

During springtime, the Arctic atmospheric boundary layer undergoes frequent rapid depletions in ozone and gaseous elemental mercury due to reactions with halogen atoms, influencing atmospheric composition and pollutant fate. Although bromine chemistry has been shown to initiate ozone depletion events, and it has long been hypothesized that iodine chemistry may contribute, no previous measurements of molecular iodine (I₂) have been reported in the Arctic. Iodine chemistry also contributes to atmospheric new particle formation and therefore cloud properties and radiative forcing. Here we present Arctic atmospheric I2 and snowpack iodide (I-) measurements, which were conducted near Utqiagvik, AK, in February 2014. Using chemical ionization mass spectrometry, I2 was observed in the atmosphere at mole ratios of 0.3–1.0 ppt, and in the snowpack interstitial air at mole ratios up to 22 ppt under natural sunlit conditions and up to 35 ppt when the snowpack surface was artificially irradiated, suggesting a photochemical production mechanism. Further, snow meltwater I-measurements showed enrichments of up to ~1,900 times above the seawater ratio of I-/Na+, consistent with iodine activation and recycling. Modeling shows that observed I₂ levels are able to significantly increase ozone depletion rates, while also producing iodine monoxide (IO) at levels recently observed in the Arctic. These results emphasize the significance of iodine chemistry and the role of snowpack photochemistry in Arctic atmospheric composition, and imply that I₂ is likely a dominant source of iodine atoms in the Arctic.

Test of active coal capacity for retaining gaseous effluents contaminated by 131 I

International Nuclear Information System (INIS)

Campeanu, Catalina; Cruceru, Madalina; Neacsu, Elena

1999-01-01

The aim of this paper is to test the retaining capacity of the active coal of the filters for gaseous effluents contaminated by 131 I. The active coal filters are design for equipping ventilation installations of nuclear plants in which radioactive iodine and combination of it were produced and handled. Such active coal filters are provided also to sorbonnes for radiochemical and physical handling of radioactive iodine. Testing the retaining capacity of active coal for filters is an obvious step, particularly, when the material was stored long time after preparation

A wine tour around the world traced with {sup 129}I; potential as a forensic tool

Energy Technology Data Exchange (ETDEWEB)

Fitoussi, C., E-mail: caroline.fitoussi@erdw.ethz.c [Centre de Spectrometrie Nucleaire et de Spectrometrie de Masse (CSNSM) IN2P3/CNRS, Universite Paris Sud, Bat 108, 91405 Orsay (France); Raisbeck, G.M. [Centre de Spectrometrie Nucleaire et de Spectrometrie de Masse (CSNSM) IN2P3/CNRS, Universite Paris Sud, Bat 108, 91405 Orsay (France); Hubert, P. [Centre d' Etudes Nucleaires de Bordeaux Gradignan (CENBG) IN2P3/CNRS, 33175 Gradignan (France)

2010-04-15

Various quantities of anthropogenic {sup 129}I have been released out worldwide in the last decades, principally by nuclear reprocessing plants in England and France. This work was a preliminary attempt to exploit the spatial and temporal variability of these emissions to investigate the possibility of tracing the provenance and age of wines worldwide. Using carrier free iodine extraction followed by measurements by Accelerator Mass Spectrometry (AMS) at the Tandetron of Gif-sur-Yvette, we find a good correlation between the distribution of {sup 129}I/{sup 127}I and the extent to which {sup 129}I releases are expected as a function of the geographical setting. {sup 129}I concentrations, also measured in wines using the same method but with a carrier, show the same pattern.

Automation system for quality control in manufacture of iodine-125 sealed sources used in brachytherapy

International Nuclear Information System (INIS)

Somessari, Samir L.; Feher, Anselmo; Sprenger, Francisco E.; Rostellato, Maria E.C.M.; Moura, Joao A.; Costa, Osvaldo L.; Calvo, Wilson A.P.

2011-01-01

The objective of this work is to develop an automation system for Quality Control in the production of Iodine-125 sealed sources, after undergoing the process of laser beam welding. These sources, also known as Iodine-125 seeds are used, successfully, in the treatment of cancer by brachytherapy, with low-dose rates. Each small seed is composed of a welded titanium capsule with 0.8 mm diameter and 4.5 mm in length, containing Iodine-125 adsorbed on an internal silver wire. The seeds are implanted in the human prostate to irradiate the tumor and treat the cancerous cells. The technology to automate the quality control system in the manufacture of Iodine-125 seeds consists in developing and associate mechanical parts, electronic components and pneumatic circuits to control machines and processes. The automation technology for Iodine-125 seed production developed in this work employs programmable logic controller, step motors, drivers of control, electrical-electronic interfaces, photoelectric sensors, interfaces of communication and software development. Industrial automation plays an important role in the production of Iodine-125 seeds, with higher productivity and high standard of quality, facilitating the implementation and operation of processes with good manufacturing practices. Nowadays, the Radiation Technology Center at IPEN-CNEN/SP imports and distributes 36,000 Iodine-125 seeds per year for clinics and hospitals in the whole country. However, the Brazilian potential market is of 8,000 Iodine-125 seeds per month. Therefore, the local production of these radioactive seeds has become a priority for the Institute, aiming to reduce the price and increase the supply to the population in Brazil. (author)

Automation system for quality control in manufacture of iodine-125 sealed sources used in brachytherapy

Energy Technology Data Exchange (ETDEWEB)

Somessari, Samir L.; Feher, Anselmo; Sprenger, Francisco E.; Rostellato, Maria E.C.M.; Moura, Joao A.; Costa, Osvaldo L.; Calvo, Wilson A.P., E-mail: somessar@ipen.b, E-mail: afeher@ipen.b, E-mail: sprenger@ipen.b, E-mail: elisaros@ipen.b, E-mail: olcosta@ipen.b, E-mail: wapcalvo@ipen.b [Instituto de Pesquisas Energeticas e Nucleares (IPEN/CNEN-SP), Sao Paulo, SP (Brazil)

2011-07-01

The objective of this work is to develop an automation system for Quality Control in the production of Iodine-125 sealed sources, after undergoing the process of laser beam welding. These sources, also known as Iodine-125 seeds are used, successfully, in the treatment of cancer by brachytherapy, with low-dose rates. Each small seed is composed of a welded titanium capsule with 0.8 mm diameter and 4.5 mm in length, containing Iodine-125 adsorbed on an internal silver wire. The seeds are implanted in the human prostate to irradiate the tumor and treat the cancerous cells. The technology to automate the quality control system in the manufacture of Iodine-125 seeds consists in developing and associate mechanical parts, electronic components and pneumatic circuits to control machines and processes. The automation technology for Iodine-125 seed production developed in this work employs programmable logic controller, step motors, drivers of control, electrical-electronic interfaces, photoelectric sensors, interfaces of communication and software development. Industrial automation plays an important role in the production of Iodine-125 seeds, with higher productivity and high standard of quality, facilitating the implementation and operation of processes with good manufacturing practices. Nowadays, the Radiation Technology Center at IPEN-CNEN/SP imports and distributes 36,000 Iodine-125 seeds per year for clinics and hospitals in the whole country. However, the Brazilian potential market is of 8,000 Iodine-125 seeds per month. Therefore, the local production of these radioactive seeds has become a priority for the Institute, aiming to reduce the price and increase the supply to the population in Brazil. (author)

Iodine deficiency and subclinical hypothyroidism are common in cystic fibrosis patients.

Science.gov (United States)

Naehrlich, Lutz; Dörr, Helmuth-Günther; Bagheri-Behrouzi, Azadeh; Rauh, Manfred

2013-04-01

Disorders of thyroid function have been inconsistently described in cystic fibrosis (CF) patients and in CF transmembrane regulator protein knockout animals. The literature lacks reports on iodine status of CF individuals. We hypothesize, that iodine deficiency is common in CF and account for abnormal thyroid function in CF patients. We investigated 129 children, adolescents, and adults with CF, who were living in the northern part of Bavaria/Germany. Malnutrition and lung function were analyzed. Urinary iodine excretion, TSH (thyroid-stimulating hormone), and ft4 (free thyroxine) were measured and set in relation to population-based, age-adjusted reference ranges. Subclinical hypothyroidism (normal fT4, elevated TSH) was found in 11.6% of subjects, and iodine deficiency in 83.7%. No correlations were found with age, BMI, status of malnutrition, or lung function. Dramatic iodine deficiency was found in our cohort of CF patients. This condition can cause subclinical hypothyroidism; therefore, an individual iodine supplementation program is necessary and should be started immediately. Crown Copyright © 2012. Published by Elsevier GmbH. All rights reserved.

Radiolytic oxidation of iodine in the containment at high temperature and dose rate

International Nuclear Information System (INIS)

Guilbert, S.; Bosland, L.; Jacquemain, D.; Clement, B.; Andreo, F.; Ducros, G.; Dickinson, S.; Herranz, L.; Ball, J.

2007-01-01

Iodine Chemistry is one of the areas of top interest in the field of nuclear power plants (NPP) severe accidents studies. The strong radiological impact of iodine on man health and environment, mostly through its isotope I-131, has made it a key point to get an accurate prediction of the potential iodine release from the NPP containment to the environment in the low probable event of an accident leading to core melt. Released from the fuel as a gaseous form, iodine enters the containment in gaseous or particulate form and undergoes deposition processes that eventually take it to the containment surfaces and sump. Once in the sump, iodine, when present as soluble compounds, gets dissolved as non volatile iodide (I-). Nonetheless, in the presence of radiation and particularly in acidic sumps, iodine can be oxidized to volatile forms such as molecular iodine (I 2 ) and can escape from the sump to the containment atmosphere (sump radiolysis process), thus increasing its potential contribution to the iodine source term. Iodine sump radiolysis has been extensively studied experimentally in the past decades. Experiments have revealed that parameters such as pH, temperature and total iodine concentration have a large impact on iodine volatility. However, experimental data at elevated temperatures (> 80 O C) and elevated dose rates (> 1 kGy.h -1 ) anticipated in containment during a postulated severe accident are too scarce to provide for these relevant conditions an accurate determination of the volatile iodine fractions. Furthermore, some data were obtained from post-irradiation analysis and iodine concentration may be underestimated at the time of measurements compared with that during irradiation, due to post-irradiation reactions. To complete the existing database, the EPICUR program was launched by IRSN (Institut de Radioprotection et de Surete Nucleaire) and experiments have been performed in the frame of the International Source Term Program (ISTP) to provide on

Adsorption and revaporisation studies on iodine oxide aerosols deposited on containment surface materials in LWR

Energy Technology Data Exchange (ETDEWEB)

Tietze, S.; Foreman, M.R.StJ.; Ekberg, C. [Chalmers Univ. of Technology, Goeteborg (Sweden); Kaerkelae, T.; Auvinen, A.; Tapper, U.; Lamminmaeki, S.; Jokiniemi, J. [VTT Technical Research Centre of Finland, Espoo (Finland)

2012-12-15

During a hypothetical severe nuclear accident, the radiation field will be very high in the nuclear reactor containment building. As a result gaseous radiolysis products will be formed. Elemental iodine can react in the gaseous phase with ozone to form solid iodine oxide aerosol particles (iodine oxide). Within the AIAS (Adsorption of Iodine oxide Aerosols on Surfaces) project the interactions of iodine oxide (IOx) aerosols with common containment surface materials were investigated. Common surface materials in Swedish and Finnish LWRs are Teknopox Aqua V A paint films and metal surfaces such as Cu, Zn, Al and SS, as well as Pt and Pd surfaces from hydrogen recombiners. Non-radioactive and {sup 131}I labelled iodine oxide aerosols were produced with the EXSI CONT facility from elemental iodine and ozone at VTT Technical Research Centre of Finland. The iodine oxide deposits were analysed with microscopic and spectroscopic measurement techniques to identify the kind of iodine oxide formed and if a chemical conversion on the different surface materials occurs. The revaporisation behaviour of the deposited iodine oxide aerosol particles from the different surface materials was studied under the influence of heat, humidity and gamma irradiation at Chalmers University of Technology, Sweden. Studies on the effects of humidity were performed using the FOMICAG facility, while heat and irradiation experiments were performed in a thermostated heating block and with a gammacell 22 having a dose rate of 14 kGy/h. The revaporisation losses were measured using a HPGe detector. The revaporisated {sup 131}I species from the surfaces were chemically tested for elemental iodine formation. The parameter dominating the degradation of the produced iodine oxide aerosols was humidity. Cu and Zn surfaces were found to react with iodine from the iodine oxide aerosols to form iodides, while no metal iodides were detected for Al and SS samples. Most of the iodine oxide aerosols are assumed to

Influence of excessive iodine intake on the thyroid function and spectrum of thyroid abnormalities in population of Turinsk, Sverdlovsk Region, of Russia

Directory of Open Access Journals (Sweden)

Aleksey V. Kiyaev

2015-05-01

Full Text Available Background. Previous surveys showed chronic iodine excess - median urinary iodine concentration (UIC over 500 mcg/l — supposedly due to water contamination in population of Turinsk, a town in Sverdlovsk Region of Russia. Aim. Conduct an assessment of the effects of chronic iodine excess on thyroid function and spectrum of thyroid abnormalities in schoolchildren and adults. Materials and methods. Assessment was conducted in 100 schoolchildren and 100 adults residing in Turinsk and 97 schoolchildren and 100 adults in the control site (city of Pervouralsk with optimal UIC. Assessment included thyroid ultrasonogrpahy, urinary iodine and dry spot TSH in schoolchildren and TSH and TPO-ab in adults. Iodine was also measured in random water samples from 10 households in Turinsk. Results. Median UIC in schoolchildren in Turinsk (719 mcg/l was significantly higher (129 mcg/l than in Pervouralsk resulting in higher prevalence of thyroid enlargement and TSH level. In adults TSH level as well as prevalence of sub-clinical hypothyroidism and autoimmune thyroiditis were higher in residents of Turinsk compared to control group from Pervouralsk. Conclusions. Iodine excess alters thyroid function in schoolchildren and adults increasing prevalence of thyroid enlargement in children and autoimmune thyroidis in adults.

Comments on the paper 'Radiation doses from iodine-129 in the environment' by J. K. Soldat

Energy Technology Data Exchange (ETDEWEB)

Thompson, Jr, J C [Cornell Univ., Ithaca, N.Y. (USA)

1976-09-01

Reference is made to a recent article by Soldat entitled 'Radiation Doses from /sup 129/I in the Environment' (Health Phys. Jan 1976) in which it is claimed that human and bovine consumption estimates were used in arriving at /sup 129/I thyroid doses which do not conform to observed consumption data. It is claimed that the disparity between the consumption data for milk, leafy vegetable and beef and the feed intake estimates for beef cattle is sufficient to produce /sup 129/I thyroid dose estimates that are considerably elevated. Using consumption data here advocated a modified table of thyroid dose estimates from unit concentrations of /sup 129/I in air is presented.

Iodine immobilization in apatites

International Nuclear Information System (INIS)

Audubert, F.; Lartigue, J.E.

2000-01-01

In the context of a scientific program on long-lived radionuclide conditioning, a matrix for iodine 129 immobilization has been studied. A lead vanado-phosphate apatite was prepared from the melt of lead vanado-phosphate Pb 3 (VO 4 ) 1.6 (PO 4 ) 0.4 and lead iodide PbI 2 in stoichiometric proportions by calcination at 700 deg. C during 3 hours. Natural sintering of this apatite is not possible because the product decomposition occurs at 400 deg. C. Reactive sintering is the solution. The principle depends on the coating of lead iodide with lead vanado-phosphate. Lead vanado-phosphate coating is used as iodo-apatite reactant and as dense covering to confine iodine during synthesis. So the best condition to immobilize iodine during iodo-apatite synthesis is a reactive sintering at 700 deg. C under 25 MPa. We obtained an iodo-apatite surrounded with dense lead vanadate. Leaching behaviour of the matrix synthesized by solid-solid reaction is under progress in order to determine chemical durability, basic mechanisms of the iodo-apatite alteration and kinetic rate law. Iodo-apatite dissolution rates were pH and temperature dependent. We obtained a rate of 2.5 10 -3 g.m -2 .d -1 at 90 deg. C in initially de-ionised water. (authors)

Sequestration and remobilization of radioiodine (129I) by soil organic matter and possible consequences of the remedial action at Savannah River Site.

Science.gov (United States)

Xu, Chen; Miller, Eric J; Zhang, Saijin; Li, Hsiu-Ping; Ho, Yi-Fang; Schwehr, Kathleen A; Kaplan, Daniel I; Otosaka, Shigeyoshi; Roberts, Kimberly A; Brinkmeyer, Robin; Yeager, Chris M; Santschi, Peter H

2011-12-01

In order to investigate the distributions and speciation of (129)I (and (127)I) in a contaminated F-Area groundwater plume of the Savannah River Site that cannot be explained by simple transport models, soil resuspension experiments simulating surface runoff or stormflow and erosion events were conducted. Results showed that 72-77% of the newly introduced I(-) or IO(3)(-) were irreversibly sequestered into the organic-rich riparian soil, while the rest was transformed by the soil into colloidal and truly dissolved organo-iodine, resulting in (129)I remobilization from the soil greatly exceeding the 1 pCi/L drinking water permit. This contradicts the conventional view that only considers I(-) or IO(3)(-) as the mobile forms. Laboratory iodination experiments indicate that iodine likely covalently binds to aromatic structures of the soil organic matter (SOM). Under very acidic conditions, abiotic iodination of SOM was predominant, whereas under less acidic conditions (pH ≥5), microbial enzymatically assisted iodination of SOM was predominant. The organic-rich soil in the vadose zone of F-Area thus acts primarily as a "sink," but may also behave as a potentially important vector for mobile radioiodine in an on-off carrying mechanism. Generally the riparian zone provides as a natural attenuation zone that greatly reduces radioiodine release.

Raim – A model for iodine behavior in containment under severe accident condition

Directory of Open Access Journals (Sweden)

Han-Chul Kim

2015-12-01

Full Text Available Following a severe accident in a nuclear power plant, iodine is a major contributor to the potential health risks for the public. Because the amount of iodine released largely depends on its volatility, iodine's behavior in containment has been extensively studied in international programs such as International Source Term Programme-Experimental Program on Iodine Chemistry under Radiation (EPICUR, Organization for Economic Co-operation and Development (OECD-Behaviour of Iodine Project, and OECD-Source Term Evaluation and Mitigation. Korea Institute of Nuclear Safety (KINS has joined these programs and is developing a simplified, stand-alone iodine chemistry model, RAIM (Radio-Active Iodine chemistry Model, based on the IMOD methodology and other previous studies. This model deals with chemical reactions associated with the formation and destruction of iodine species and surface reactions in the containment atmosphere and the sump in a simple manner. RAIM was applied to a simulation of four EPICUR tests and one Radioiodine Test Facility test, which were carried out in aqueous or gaseous phases. After analysis, the results show a trend of underestimation of organic and molecular iodine for the gas-phase experiments, the opposite of that for the aqueous-phase ones, whereas the total amount of volatile iodine species agrees well between the experiment and the analysis result.

Advanced chemical oxygen iodine lasers for novel beam generation

Science.gov (United States)

Wu, Kenan; Zhao, Tianliang; Huai, Ying; Jin, Yuqi

2018-03-01

Chemical oxygen iodine laser, or COIL, is an impressive type of chemical laser that emits high power beam with good atmospheric transmissivity. Chemical oxygen iodine lasers with continuous-wave plane wave output are well-developed and are widely adopted in directed energy systems in the past several decades. Approaches of generating novel output beam based on chemical oxygen iodine lasers are explored in the current study. Since sophisticated physical processes including supersonic flowing of gaseous active media, chemical reacting of various species, optical power amplification, as well as thermal deformation and vibration of mirrors take place in the operation of COIL, a multi-disciplinary model is developed for tracing the interacting mechanisms and evaluating the performance of the proposed laser architectures. Pulsed output mode with repetition rate as high as hundreds of kHz, pulsed output mode with low repetition rate and high pulse energy, as well as novel beam with vector or vortex feature can be obtained. The results suggest potential approaches for expanding the applicability of chemical oxygen iodine lasers.

Determination of 129I/127I isotope ratios in liquid solutions and environmental soil samples by ICP-MS with hexapole collision cell

OpenAIRE

Izmer, A. V.; Boulyga, S. F.; Becker, J. S.

2003-01-01

The determination of I-129 in environmental samples at ultratrace levels is very difficult by ICP-MS due to a high noise caused by Xe impurities in argon plasma gas (interference of Xe-129(+)), possible (IH2+)-I-127 interference and an insufficient abundance ratio sensitivity of the ICP mass spectrometer for I-129/I-127 isotope ratio measurement. A sensitive, powerful and fast analytical technique for iodine isotope ratio measurements in aqueous solutions and contaminated soil samples directl...

High pressure 129I Moessbauer studies of GeI4 molecular crystals

International Nuclear Information System (INIS)

Pasternak, M.P.; Taylor, R.D.

1989-01-01

The Moessbauer effect in 129 I in conjunction with Diamond-Anvil-Cell high pressure techniques was applied to investigate the high pressure phase(s) of the molecular crystal GeI 4 . The 129 I Quadrupole Interaction was the main probe for characterizing the intermolecular structural transformation with pressure. With increasing pressure, at about 15 GPAa, the onset of a partial molecular-association phase (HP1) is first observed. In HP1 two out of the four iodines strongly overlap to form linear chains of GeI 4 . The HP1 phase coexists with the low pressure (LP) molecular phase, but its population increases with increasing pressure. At P ∼20 GPa a second high pressure phase (HP2) is identified where all four iodines strongly overlap to form a three dimensional, fully molecular-associated structure. With increasing pressure and at P > 20 GPa, HP2 is the only phase up to P = 34 GPa, the highest pressure used. A significant hysteresis of the relative abundances with pressure is observed. The isomer shift of the HP2 and HP1 structures is considerably larger than that of the LP one. 11 refs., 3 figs

High pressure 129I Moessbauer studies of GeI4 molecular crystals

International Nuclear Information System (INIS)

Pasternak, M.P.; Los Alamos National Lab.; Taylor, R.D.

1990-01-01

The Moessbauer effect in 129 I in cunjunction with Diamond-Anvil-Cell high pressure techniques was applied to investigate the high pressure phase(s) of the molecular crystal GeI 4 . The 129 I Quadrupole Interaction was the main probe for characterizing the intermolecular structural transformation with pressure. With increasing pressure, at about 15 GPa, the onset of a partial molecular-association phase (HP1) is first observed. In HP1 two out of the four iodines strongly overlap to form linear chains of GeI 4 . The HP1 phase coexists with the low pressure (LP) molecular phase, but its population increases with increasing pressure. At P≅20 GPa a second high pressure phase (HP2) is identified where all four iodines strongly overlap to form a three dimensional, fully molecular-associated structure. With increasing pressure and at P>20 GPa, HP2 is the only phase up to P=34 GPa, the highest pressure used. A significant hysteresis of the relative abundances with pressure is observed. The isomer shift of the HP2 and HP1 structures is considerably larger than that of the LP one. (orig.)

A summary of global {sup 129}I in marine waters

Energy Technology Data Exchange (ETDEWEB)

He Peng, E-mail: peng.he@geo.uu.se [Dept. of Earth Sciences, Uppsala University, Villav. 16, 752 36 Uppsala (Sweden); Aldahan, A. [Dept. of Earth Sciences, Uppsala University, Villav. 16, 752 36 Uppsala (Sweden); Dept. of Geology, United Arab Emirates University, P.O. Box 17551, Al Ain (United Arab Emirates); Possnert, G. [Tandem Laboratory, Uppsala University, P.O. Box 529, 751 20 Uppsala (Sweden); Hou, X.L. [Riso National Laboratory for Sustainable Energy, NUK-202, Technical University of Denmark, DK-4000 Roskilde (Denmark)

2013-01-15

Despite the many investigations concerning the occurrence of anthropogenic iodine-129 in the atmosphere, terrestrial and marine environments, there is a lack of a comprehensive collection of data on the distribution of the isotope in marine waters. The temporal and spatial variability of anthropogenic {sup 129}I is strongly linked to the major point sources in the Irish Sea and the English Channel and the global marine spreading pathways are partly outlined from these sources. The temporal evolution is still, however, not well defined when transport and dissipation are considered in the different oceans and ocean compartments. We here summarize available published literature data on {sup 129}I temporal and spatial distribution in the global marine water. The results show presence of numerous data sets for the North Atlantic and Arctic Oceans where strong variability in terms of water depth, time and location also occur. Scarcity of data on {sup 129}I from the Pacific, Indian and South Atlantic Oceans demonstrates gaps in the coverage of the isotope spatial extent. These shortcomings in the spatial coverage may relate to the understanding that the anthropogenic {sup 129}I signal will take a long time to be transported, if at all, from the North Atlantic into other oceans. Data from recent expeditions in the Southern oceans and the Geotraces ocean profiling will reveal additional information about {sup 129}I distribution in the marine waters.

Dry deposition of gaseous radioiodine and particulate radiocaesium onto leafy vegetables

Energy Technology Data Exchange (ETDEWEB)

Tschiersch, Jochen, E-mail: tschiersch@helmholtz-muenchen.de [Helmholtz Zentrum Muenchen, German Research Center for Environmental Health, Institute of Radiation Protection, Ingolstaedter Landstr. 1, 85764 Neuherberg (Germany); Shinonaga, Taeko [Helmholtz Zentrum Muenchen, German Research Center for Environmental Health, Institute of Radiation Protection, Ingolstaedter Landstr. 1, 85764 Neuherberg (Germany); Heuberger, Heidi [TU Muenchen, Center of Life and Food Sciences Weihenstephan, Duernast 2, 85350 Freising (Germany)

2009-10-15

Radionuclides released to the atmosphere during dry weather (e.g. after a nuclear accident) may contaminate vegetable foods and cause exposure to humans via the food chain. To obtain experimental data for an appropriate assessment of this exposure path, dry deposition of radionuclides to leafy vegetables was studied under homogeneous and controlled greenhouse conditions. Gaseous {sup 131}I-tracer in predominant elemental form and particulate {sup 134}Cs-tracer at about 1 {mu}m diameter were used to identify susceptible vegetable species with regard to contamination by these radionuclides. The persistence was examined by washing the harvested product with water. The vegetables tested were spinach (Spinacia oleracea), butterhead lettuce (Lactuca sativa var. capitata), endive (Cichorium endivia), leaf lettuce (Lactuca sativa var. crispa), curly kale (Brassica oleracea convar. acephala) and white cabbage (Brassica oleracea convar. capitata). The variation of radionuclides deposited onto each vegetable was evaluated statistically using the non-parametric Kruskal-Wallis Test and the U-test of Mann-Whitney. Significant differences in deposited {sup 131}I and {sup 134}Cs activity concentration were found among the vegetable species. For {sup 131}I, the deposition velocity to spinach normalized to the biomass of the vegetation was 0.5-0.9 cm{sup 3} g{sup -1} s{sup -1} which was the highest among all species. The particulate {sup 134}Cs deposition velocity of 0.09 cm{sup 3} g{sup -1} s{sup -1} was the highest for curly kale, which has rough and structured leaves. The lowest deposition velocity was onto white cabbage: 0.02 cm{sup 3} g{sup -1} s{sup -1} (iodine) and 0.003 cm{sup 3} g{sup -1} s{sup -1} (caesium). For all species, the gaseous iodine deposition was significantly higher compared to the particulate caesium deposition. The deposition depends on the sensitive parameters leaf area, stomatal aperture, and plant morphology. Decontamination by washing with water was very

Effect of interfering reactions on the determination of iodine-129 concentrations in the enviroment by activation analysis

International Nuclear Information System (INIS)

Filistovich, V.; Nedvetskajte, T.

1985-01-01

The influence of the interfering reactions sup(235)U(n, f) sup(129)In(n, γ)sup(130)I, sup(128)Te(n, γ)sup(129)Te, sup(129)Te(Tsub(1/2)sup(βsup(-))=69.6 min) sup(129)I(n, γ)sup(130)I and sup(127)I(3n, γ)sup(130)I on the measurements by the activation analysis method of the background sup(129)I concentrations in the environment has been investigated. The calculations have shown that these reactions may result in considerable errors. A pretreatment of samples before their irradiation in a reactor is therefore needed. It is recommended to use the destructive distillation method. A nomogram is given with the help of which it is possible to determine the optimal time for the sample irradiation in the reactor after the sup(127)I concentrations have bee nevaluated in the samples, because the considerable amount of the sup(129)I can be generated from the sup(127)I by the triple neutron capture

Ultratrace analysis of {sup 129}I in sediments by ICP-MS with collision cell

Energy Technology Data Exchange (ETDEWEB)

Izmer, A.V.; Becker, J.S. [Research Center Juelich (Germany). Central Div. of Analytical Chemistry; Boulyga, S.F. [Mainz Univ. (Germany). Inst. for Inorganic Chemistry and Analytical Chemistry; Zoriy, M.V. [Research Center Juelich (Germany). Central Div. of Analytical Chemistry]|[Research Center Juelich (Germany). Dept. for Safety and Radiation Protection

2004-07-01

The aim of the work was the development of a rapid and high-sensitive analytical method using ICP-MS with hexapole collision cell (ICP-CC-MS) for the determination of low 129I+/127I+ isotope ratios in synthetic lab standards and environmental samples. A special direct sample introduction device for iodine extraction via the gas phase from solid environmental material coupled on-line to ICP-CC-QMS was developed. The detection limit for 129I+ determination in aqueous solution and soil samples via gas-phase extraction was determined to be of 0.8 pg/g and 30 pg/g, respectively. (orig.)

Behavior of iodine in the dissolution of spent nuclear fuels

Energy Technology Data Exchange (ETDEWEB)

Sakurai, Tsutomu; Komatsu, Kazunori; Takahashi, A. [Japan Atomic Energy Research Institute, Ibaraki-ken (Japan)

1997-08-01

The results of laboratory-scale experiments concerning the behavior of iodine in the dissolution of spent nuclear fuels, which were carried out at the Japan Atomic Energy Research Institute, are summarized. Based on previous and new experimental results, the difference in quantity of residual iodine in the fuel solution between laboratory-scale experiments and reprocessing plants is discussed, Iodine in spent fuels is converted to the following four states: (1) oxidation into I{sub 2} by nitric acid, (2) oxidation into I{sub 2} by nitrous acid generated in the dissolution, (3) formation of a colloid of insoluble iodides such as AgI and PdI{sub 2}, and (4) deposition on insoluble residue. Nitrous acid controls the amount of colloid formed. As a result, up to 10% of iodine in spent fuels is retained in the fuel solution, up to 3% is deposited on insoluble residue, and the balance volatilizes to the off-gas, Contrary to earlier belief, when the dissolution is carried out in 3 to 4 M HNO{sub 3} at 100{degrees}C, the main iodine species in a fuel solution is a colloid, not iodate, Immediately after its formation, the colloid is unstable and decomposes partially in the hot nitric acid solution through the following reaction: AgI(s) + 2HNO{sub 3}(aq) = {1/2}I{sub 2}(aq) + AgNO{sub 3}(aq) + NO{sub 2}(g) + H{sub 2}O(1). For high concentrations of gaseous iodine, I{sub 2}(g), and NO{sub 2}, this reaction is reversed towards formation of the colloid (AgI). Since these concentrations are high near the liquid surface of a plant-scale dissolver, there is a possibility that the colloid is formed there through this reversal, Simulations performed in laboratory-scale experiments demonstrated this reversal, This phenomenon can be one reason the quantity of residual iodine in spent fuels is higher in reprocessing plants than in laboratory-scale experiments. 17 refs., 5 figs., 3 tabs.

Study of iodine removal efficiency in self-priming venturi scrubber

International Nuclear Information System (INIS)

Ali, Majid; Yan, Changqi; Sun, Zhongning; Gu, Haifeng; Wang, Junlong

2013-01-01

Highlights: ► Study of iodine removal efficiency in a self-priming venturi scrubber. ► Investigation of iodine removal efficiency at different gas and liquid flow rates. ► Investigation of different inlet concentrations of iodine. ► Mathematical model based on mass transfer. - Abstract: Venturi scrubber is used in filtered vented containment system of nuclear power plants to remove the gaseous pollutants from contaminated gas during severe accidents. In this research, an experimental and theoretical investigation has been carried out to study the iodine removal efficiency in a self-priming venturi scrubber. The aqueous solution is prepared by adding weight percentage of sodium hydroxide 0.5% and sodium thiosulphate 0.2% in scrubbing water to increase the absorbance of inorganic iodine (I 2 ) from the contaminated gas during emission. The iodine removal efficiency is investigated at various gas and liquid flow rates, and iodine inlet concentrations. The iodine removal efficiency is measured experimentally by measuring the inlet and outlet concentration of iodine at sampling ports. The petite droplets are formed in a venturi scrubber to absorb the iodine through the mass transfer phenomenon. A mathematical model for mass transfer based on a gas liquid interface is employed for the verification of experimental results. The contact time between iodine and scrubbing solution depends on the total volumetric flow of gas and liquid, and volume of throat and diffuser of the venturi scrubber. Sauter mean diameter is calculated from the Nukiyama and Tanasawa correlation. Steinberger and Treybal’s correlation is used to measure the mass transfer coefficient for the gas phase. The results calculated from the model under predict the experimental data

Glass composite waste forms for iodine confined in bismuth-embedded SBA-15

Science.gov (United States)

Yang, Jae Hwan; Park, Hwan Seo; Ahn, Do-Hee; Yim, Man-Sung

2016-11-01

The aim of this study was to stabilize bismuth-embedded SBA-15 that captured iodine gas by fabrication of monolithic waste forms. The iodine containing waste was mixed with Bi2O3 (a stabilizing additive) and low-temperature sintering glass followed by pelletizing and the sintering process to produce glass composite materials. Iodine volatility during the sintering process was significantly affected by the ratio of Bi2O3 and the glass composition. It was confirmed that BiI3, the main iodine phase within bismuth-embedded SBA-15, was effectively transformed to the mixed phases of Bi5O7I and BiOI. The initial leaching rates of iodine from the glass composite waste forms ranged 10-3-10-2 g/m2 day, showing the stability of the iodine phases encapsulated by the glassy networks. It was also observed that common groundwater anions (e.g., chloride, carbonate, sulfite, and fluoride) elevated the iodine leaching rate by anion exchange reactions. The present results suggest that the glass composite waste form of bismuth-embedded SBA-15 could be a candidate material for stable storage of 129I.

Distribution of 129I: Evidence for world-wide influence of nuclear fuel reprocessing

International Nuclear Information System (INIS)

Fehn, U.; Snyder, G.; Moran, J.E.

1999-01-01

Iodine-129 is one of the radioisotopes which have seen significant increases in the environment since the beginning of the nuclear age. Other prominent representatives of this group include tritium, 14 C and 36 Cl. Most members of this group have gone through a cycle of initial release (associated mainly with atmospheric bomb tests during the late fifties and early sixties) and subsequent decay (e.g. T) or dispersion (e.g. 14 C and 36 Cl) so that their concentrations are again close to pre-anthropogenic levels. 129 I has, however, remained at significantly elevated levels even after the stop of nuclear weapon tests

Shuttle Gaseous Hydrogen Venting Risk from Flow Control Valve Failure

Science.gov (United States)

Drummond, J. Philip; Baurle, Robert A.; Gafney, Richard L.; Norris, Andrew T.; Pellett, Gerald L.; Rock, Kenneth E.

2009-01-01

This paper describes a series of studies to assess the potential risk associated with the failure of one of three gaseous hydrogen flow control valves in the orbiter's main propulsion system during the launch of Shuttle Endeavour (STS-126) in November 2008. The studies focused on critical issues associated with the possibility of combustion resulting from release of gaseous hydrogen from the external tank into the atmosphere during assent. The Shuttle Program currently assumes hydrogen venting from the external tank will result in a critical failure. The current effort was conducted to increase understanding of the risk associated with venting hydrogen given the flow control valve failure scenarios being considered in the Integrated In-Flight Anomaly Investigation being conducted by NASA.

Can an Educational Intervention Improve Iodine Nutrition Status in Pregnant Women? A Randomized Controlled Trial.

Science.gov (United States)

Amiri, Parisa; Hamzavi Zarghani, Najmeh; Nazeri, Pantea; Ghofranipour, Fazlollah; Karimi, Mehrdad; Amouzegar, Atieh; Mirmiran, Parvin; Azizi, Fereidoun

2017-03-01

Because of their increased need for iodine, pregnant women are among the high-risk groups for iodine deficiency. The purpose of this study was to evaluate the effectiveness of an educational program on the iodine nutrition status of pregnant women. In this randomized controlled trial, 100 pregnant women were randomly selected from five healthcare centers in the southern region of Tehran, the capital of Iran. In the intervention group, pregnant women received a four-month educational program, which included two face-to-face educational sessions, using a researcher-designed educational pamphlet in the second and third trimesters, and two follow-up telephone calls. Knowledge, attitude, and practice (KAP) scores, urinary iodine concentration (UIC), and salt iodine content were assessed at baseline and four months after the intervention. At baseline, there were significant associations between knowledge and attitude (r = 0.38, p = 0.03) between practice and UIC (r = 0.28, p = 0.01) and between UIC and iodine content of salt (r = 0.24, p = 0.009). Although a significant difference was found in mean KAP scores between the two groups after the educational intervention, scores were significantly higher in the intervention group compared with controls (p educational intervention increasing KAP among women regarding the importance of iodine and iodized salt consumption during pregnancy, their iodine status did not improve. Considering the main socio-environmental determinants of iodine deficiency, in particular, the monitoring of salt fortification, prescribing iodine containing supplements as well as improving health literacy in pregnant women seem essential strategies.

Novel molecular-level evidence of iodine binding to natural organic matter from Fourier transform ion cyclotron resonance mass spectrometry

International Nuclear Information System (INIS)

Xu, Chen; Chen, Hongmei; Sugiyama, Yuko; Zhang, Saijin; Li, Hsiu-Ping; Ho, Yi-Fang; Chuang, Chia-ying; Schwehr, Kathleen A.; Kaplan, Daniel I.; Yeager, Chris; Roberts, Kimberly A.; Hatcher, Patrick G.; Santschi, Peter H.

2013-01-01

Major fractions of radioiodine ( 129 I) are associated with natural organic matter (NOM) in the groundwater and surface soils of the Savannah River Site (SRS). Electrospray ionization coupled to Fourier transform ion cyclotron resonance mass spectrometry (ESI-FTICR-MS) was applied to elucidate the interactions between inorganic iodine species (iodide and iodate) and a fulvic acid (FA) extracted from a SRS surface soil. Iodate is likely reduced to reactive iodine species by the lignin- and tannin-like compounds or the carboxylic-rich alicyclic molecules (CRAM), during which condensed aromatics and lignin-like compounds were generated. Iodide is catalytically oxidized into reactive iodine species by peroxides, while FA is oxidized by peroxides into more aliphatic and less aromatic compounds. Only 9% of the total identified organo-iodine compounds derived from molecules originally present in the FA, whereas most were iodine binding to newly-produced compounds. The resulting iodinated molecules were distributed in three regions in the van Krevelen diagrams, denoting unsaturated hydrocarbons, lignin and protein. Moreover, characteristics of these organo-iodine compounds, such as their relatively low O/C ratios ( 2 or -HNCOR groups and a ring-activating functionality to favor the electrophilic substitution. The ESI-FTICR-MS technique provides novel evidence to better understand the reactivity and scavenging properties of NOM towards radioiodine and possible influence of NOM on 129 I migration. Highlights: ► IO 3 − reduced by lignin-, tannin-like compounds/carboxylic-rich alicyclic molecules ► Condensed aromatic and lignin-like compounds generated after iodate-iodination ► Aliphatic and less aromatic compounds formed after iodide-iodination ► Organo-iodine identified as unsaturated hydrocarbons, lignin and protein ► Organo-iodine with low O/C ratios imply less environmental mobility

129I/127I ratios in surface waters of the English Lake District

International Nuclear Information System (INIS)

Atarashi-Andoh, M.; Schnabel, C.; Cook, G.; MacKenzie, A.B.; Dougans, A.; Ellam, R.M.; Freeman, S.; Maden, C.; Olive, V.; Synal, H.-A.; Xu, S.

2007-01-01

Accelerator Mass Spectrometry (AMS) was used to measure 129 I/ 127 I ratios in surface sea, lake, and river water samples collected in 2004 and 2005 from the English Lake District and from SW Scotland, areas which are in relatively close proximity to the Sellafield nuclear fuel reprocessing plant in NW England. The 129 I/ 127 I ratios in surface water collected from the shore of the Irish Sea were in the range 2.8 x 10 -6 to 8.2 x 10 -6 . These ratios are one order of magnitude higher than that of seawater collected from the Irish Sea in 1992, correlating with the increase in 129 I content of the Sellafield liquid effluent discharge over the last decade. The 129 I/ 127 I ratios in lakes in the Lake District were in the range 0.7 x 10 -6 to 6.4 x 10 -6 and decreased exponentially as a function of distance from Sellafield. Consideration of the relative variation of stable I concentrations and 129 I/ 127 I ratios suggests that Sellafield gaseous discharges may be the dominant source of 129 I to the lakes

Mercury and Iodine systematics of volcanic arc fluids

Science.gov (United States)

Varekamp, J. C.; Kading, T.; Fehn, U.; Lu, Z.

2008-12-01

The mantle has low Mercury and Iodine concentrations, but these elements occur in volcanic gases and hydrothermal fluids at ppb (Hg) and ppm (Iodine) levels. Possibly, the Hg and Iodine concentrations in volcanic fluids reflect subducted sediment sources in arc magmas. Iodine is a biophilic element, and I129/I values indicate that subducted sediment (especially organic matter) is an important Iodine source for arc magmas. It is uncertain if this is true for Hg as well, although in the surface environment Hg is commonly associated with organic matter. We present 60 new analyses of Hg and I in fluids from volcanoes in Central America, New Zealand, Japan, and the Cascades. A first assessment suggests that Iodine is released to some degree in the early stage of subduction in the forearc, whereas Hg may be released largely below the main volcanic arc. Isotope and trace element signatures of volcanic rocks of the investigated volcanoes show no simple correlation with Hg or Iodine abundances. The acid hot spring fluids of Copahue volcano (Argentina) carried ~ 200 ppt Hg in January 1999, ~80 ppt Hg in March 2008, and 90 ppt Hg in the crater lake in March 1997. The dissolved Hg fluxes from the Copahue hydrothermal system are ~300 gr Hg/year in 1999 and ~130 gr Hg/year in 2008. The bulk hydrothermal Hg flux (particle bound+dissolved) in 2008 was ~ 350 gr Hg/year. The potential Mercury evasion from these hydrothermal spring fluids into the air has not yet been incorporated in these estimates.

Generalised derived limits for radioisotopes of iodine

International Nuclear Information System (INIS)

Hughes, J.S.; Haywood, S.M.; Simmonds, J.R.

1984-04-01

Generalised Derived Limits (GDLs) are evaluated for iodine-125,129,131,132,133,134,135 in selected materials from the terrestrial and aquatic environments and for discharge to atmosphere. They are intended for use as convenient reference levels against which the results of environmental monitoring can be compared and atmospheric discharges assessed. GDLs are intended for use when the environmental contamination or discharge to atmosphere is less than about 5% of the GDL. If the level of environmental contamination or discharge to the atmosphere exceeds this percentage of the GDL it does not necessarily mean that the dose equivalents to members of the public are approaching the dose equivalent limit. It is rather an indication that it may be appropriate to obtain a more specific derived limit for the particular situation by reviewing the values of the parameters involved in the calculation. GDL values are specified for iodine radionuclides in water, soil, grass, sediments and various foodstuffs derived from the terrestrial and aquatic environments. GDLs are also given for iodine radionuclides on terrestrial surfaces and for their discharge to atmosphere. (author)

Iodine intake in Denmark

International Nuclear Information System (INIS)

Pedersen, K.M.; Noehr, S.B.; Laurberg, P.

1997-01-01

Iodine deficiency with a high frequency of goitre and, in severely affected areas, cretinism is common in some areas of the world. In Denmark the iodine intake as evaluated by urinary iodine excretion has been at a stable low level for many years, except for the part of the population now taking iodine supplementation as part of vitamin/mineral preparations. The iodine intake is lowest in the western part to the country where an epidemiological study of elderly subjects has demonstrated a high frequency of goitre and hyperthyroidism in women. This supports the suggestion of a controlled moderate increase in iodine intake via an iodine supplementation program. (au) 40 refs

Production of gaseous radiotracers CH{sub 3}I and I{sub 2} through Na{sup 123}I salt

Energy Technology Data Exchange (ETDEWEB)

Candeiro, R.E.M., E-mail: ricardocandeiro@cnen.gov.b [Comissao Nacional de Energia Nuclear (DIFOR/CNEN-CE), Fortaleza, CE (Brazil). Distrito de Fortaleza; Brandao, L.B. [Instituto de Engenharia Nuclear (IEN/CNEN-RJ), Rio de Janeiro, RJ (Brazil); Pereira, W.P. [Universidade Federal Fluminense (UFF), Niteroi, RJ (Brazil)

2011-07-01

The objective of the present work was to develop, separately, methodology for production of two gaseous tracers through the sodium iodide NaI marked with {sup 123}I. Found in the nature in form different, the iodine has been used in diverse works in the area of the industry and health. These two forms of the gaseous iodine, the methyl iodide, CH{sub 3}I, and molecular iodine, I{sub 2}, are very unstable and volatile in the ambient temperature and presents different problems in clean-up and monitoring systems. The syntheses were processed with sodium iodide (NaI) 1M aqueous solution marked with 1{sup 23I}. The production of gas I{sub 2} was realized with in chlorine acid (HCl) and sodium iodate salt (NaIO{sub 3}) and the CH{sub 3}I was used, the salt of NaI and the reagent (CH{sub 3}){sub 2}SO{sub 4}. The production of gases was initially realized through in unit in glass with an inert material and the purpose was to study the kinetic of reaction and to determine the efficiency of production. The two synthesis occurs in the reaction bottle and after of produced, the gas is stored in the collect bottle that contains a starch solution for fixed the I{sub 2}, and in syntheses of CH{sub 3}I contains a silver nitrate solution for your fixation. To determine the efficiency of production of gases, analytic tests were realized, where the consumption of iodide ions of the bottle of reaction are measured. The optimization of production of the each gaseous tracer was studied varying parameter as: concentration of iodide, concentration of acid and temperature. After, the syntheses of the radiotracers were realized in the compact unit, having been used as main reagent the salt radiated of sodium iodide, Na{sup 123}I. The transportation of elementary iodine and methyl iodine was studied by a scintillation detector NaI (2 x 2)' positioned in the reaction bottle. (author)

Model of iodine transport and reaction kinetics in a nuclear fuel reprocessing plant

International Nuclear Information System (INIS)

Davis, W. Jr.

1977-05-01

A model is presented to describe the time-dependent flow and retention of stable iodine isotopes and the decay of 131 I in a nuclear fuel reprocessing plant. The plant consists of 16 units of equipment such as a voloxidizer or graphite burner, fuel dissolver, solvent extractors, storage tanks, vaporizers, primary iodine sorbers, and silver zeolite. The rate of accumulation of bulk and radioactive iodine in these units and in the environment is described using 19 differential equations. Reasonable time-dependence of iodine retention factors (RFs) by the plant were calculated. RFs for a new plant in excess of 10 6 for stable iodine and 129 I decrease to the range of 10 3 to 10 2 as plant operating times exceed 50 to 100 days. The RFs for 131 I also decrease initially, for a period of approximately 10 days, but then increase by several orders of magnitude due to radioactive decay and isotopic exchange. Generally, the RFs for 131 I exceed those for stable iodine by factors of 10 4 or more. 19 references, 13 figures, 2 tables

Controlling Solid–Liquid Conversion Reactions for a Highly Reversible Aqueous Zinc–Iodine Battery

Energy Technology Data Exchange (ETDEWEB)

Pan, Huilin; Li, Bin; Mei, Donghai; Nie, Zimin; Shao, Yuyan; Li, Guosheng; Li, Xiaohong S.; Han, Kee Sung; Muller, Karl T.; Sprenkle, Vincent L.; Liu, Jun

2017-10-30

Aqueous rechargeable batteries are desirable for many energy storage applications due to their low cost and high safety. However, low capacity and short cycle life are the significant obstacles to their practical applications. Here, we demonstrate a highly reversible aqueous zinc-iodine battery using encapsulated iodine in microporous active carbon fibers (ACFs) as cathode materials through the rational control of solid-liquid conversion reactions. The experiments and density function theory (DFT) calculations were employed to investigate the effects of solvents and properties of carbon hosts, e.g. pore size, surface chemistries, on the adsorption of iodine species. The rational manipulation of the competition between the adsorption in carbon and solvation in electrolytes for iodine species is responsible for the high reversibility and cycling stability. The zinc-iodine batteries deliver a high capacity of 180 mAh g-1 at 1C and a stable cycle life over 3000 cycles with ~90% capacity retention as well as negligible self-discharge. We believe the principles for stabilizing the zinc-iodine system could provide new insight into conversion systems such as Li-S systems.

Evaluation of Iodine Remediation Technologies in Subsurface Sediments: Interim Status Report

Energy Technology Data Exchange (ETDEWEB)

Strickland, Christopher E. [Pacific Northwest National Lab. (PNNL), Richland, WA (United States); Lawter, Amanda R. [Pacific Northwest National Lab. (PNNL), Richland, WA (United States); Qafoku, Nikolla [Pacific Northwest National Lab. (PNNL), Richland, WA (United States); Szecsody, James E. [Pacific Northwest National Lab. (PNNL), Richland, WA (United States); Truex, Michael J. [Pacific Northwest National Lab. (PNNL), Richland, WA (United States); Wang, Guohui [Pacific Northwest National Lab. (PNNL), Richland, WA (United States)

2017-09-01

Isotopes of iodine were generated during plutonium production from nine production reactors at the U.S. Department of Energy Hanford Site. The long half-life 129I generated at the Hanford Site during reactor operations was 1) stored in single-shell and double-shell tanks, 2) discharged to liquid disposal sites (e.g., cribs and trenches), 3) released to the atmosphere during fuel reprocessing operations, or 4) captured by off-gas absorbent devices (silver reactors) at chemical separations plants (PUREX, B-Plant, T-Plant, and REDOX). Releases of 129I to the subsurface have resulted in several large, though dilute, plumes in the groundwater, including the plume in the 200-UP-1 operable unit. There is also 129I remaining in the vadose zone beneath disposal or leak locations. Because 129I is an uncommon contaminant, relevant remediation experience and scientific literature are limited.

Quality control of test iodine in urine by spectrophotometry UV-Vis

Science.gov (United States)

Huda, Thorikul; Nafisah, Durotun; Kumorowulan, Suryati; Lestari, Sri

2017-12-01

A quality control of iodine test in with UV-Vis spectrophotometry has been done. The purpose of this research is to find out whether the test results of samples conducted by Clinical Office of Research and Development Of GAKI (BP2GAKI) laboratory are still controlled, feasible and reliable, and still consistent over time, as indicated by the control chart. Quality control parameters are linearity, precision, accuracy, limit of detection, and limit of quantification. Based on the quality control that has been done, obtained linearity (r)= -0.9974, the detection limit and the limit of quantitation are respectively 2.26 µg/L and 7.54 µg/L, while the accuracy is calculated by %recovery and precision with value % RSD are 97.4161% and 1.7136% respectively. The quality control of iodine test in urine using the control chart shows excellent or stable results for 30 days and no variation of the results is very different for each day.

Iodine Satellite

Science.gov (United States)

Kamhawi, Hani; Dankanich, John; Martinez, Andres; Petro, Andrew

2015-01-01

The Iodine Satellite (iSat) spacecraft will be the first CubeSat to demonstrate high change in velocity from a primary propulsion system by using Hall thruster technology and iodine as a propellant. The mission will demonstrate CubeSat maneuverability, including plane change, altitude change and change in its closest approach to Earth to ensure atmospheric reentry in less than 90 days. The mission is planned for launch in fall 2017. Hall thruster technology is a type of electric propulsion. Electric propulsion uses electricity, typically from solar panels, to accelerate the propellant. Electric propulsion can accelerate propellant to 10 times higher velocities than traditional chemical propulsion systems, which significantly increases fuel efficiency. To enable the success of the propulsion subsystem, iSat will also demonstrate power management and thermal control capabilities well beyond the current state-of-the-art for spacecraft of its size. This technology is a viable primary propulsion system that can be used on small satellites ranging from about 22 pounds (10 kilograms) to more than 1,000 pounds (450 kilograms). iSat's fuel efficiency is ten times greater and its propulsion per volume is 100 times greater than current cold-gas systems and three times better than the same system operating on xenon. iSat's iodine propulsion system consists of a 200 watt (W) Hall thruster, a cathode, a tank to store solid iodine, a power processing unit (PPU) and the feed system to supply the iodine. This propulsion system is based on a 200 W Hall thruster developed by Busek Co. Inc., which was previously flown using xenon as the propellant. Several improvements have been made to the original system to include a compact PPU, targeting greater than 80 percent reduction in mass and volume of conventional PPU designs. The cathode technology is planned to enable heaterless cathode conditioning, significantly increasing total system efficiency. The feed system has been designed to

Control of interferences in the analysis of low-concentration I 129

International Nuclear Information System (INIS)

Quintana, Eduardo E.; Thyssen, Sandra M.

1999-01-01

Traces of uranium, cesium and tellurium interfere in the determination of I 129 by neutron activation analysis. The paper describes the procedures used to control or eliminate the interferences in the different steps of the analysis

Iodine-129 and Caesium-137 in Chernobyl contaminated soil and their chemical fractionation

Czech Academy of Sciences Publication Activity Database

Hou, XL.; Fogh, CL.; Kučera, Jan; Andersson, KG.; Dahlgaard, H.; Nielsen, SP.

2003-01-01

Roč. 308, 1, 2, 3 (2003), s. 97-109 ISSN 0048-9697 R&D Projects: GA AV ČR IPP1050128; GA AV ČR KSK4055109 Institutional research plan: CEZ:AV0Z1048901 Keywords : iodine * neutron activation analysis Subject RIV: DN - Health Impact of the Environment Quality Impact factor: 1.455, year: 2003

129I/127I ratios in Scottish coastal surface sea water: Geographical and temporal responses to changing emissions

International Nuclear Information System (INIS)

Schnabel, Christoph; Olive, Valerie; Atarashi-Andoh, Mariko; Dougans, Andrew; Ellam, Robert M.; Freeman, Stewart; Maden, Colin; Stocker, Martin; Synal, Hans-Arno; Wacker, Lukas; Xu Sheng

2007-01-01

This work constitutes the first survey of I isotope ratios for Scottish sea water including the first data for the west of Scotland. These data are of importance because of the proximity to the world's second largest emission source of 129 I to the sea, the Sellafield nuclear reprocessing plant, because of the increasing importance of the sea to land transfer of 129 I and also as input data for dose estimates based on this pathway of 129 I. 129 I/ 127 I ratios in SW Scotland reached 3 x 10 -6 in 2004. No strong variation of I isotope ratios was found from 2003 to 2005 in Scottish sea waters. Iodine isotope ratios increased by about a factor of 6 from 1992 to 2003 in NE Scotland, in agreement with the increase of liquid 129 I emissions from Sellafield over that time period. It is demonstrated that 129 I/ 127 I ratios agree better than 129 I concentrations for samples from similar locations taken in very close temporal proximity, indicating that this ratio is more appropriate to interpret than the radionuclide concentration

Sensitive determination of iodine species, including organo-iodine, for freshwater and seawater samples using high performance liquid chromatography and spectrophotometric detection

International Nuclear Information System (INIS)

Schwehr, Kathleen A.; Santschi, Peter H.

2003-01-01

In order to more effectively use iodine isotope ratios, 129 I/ 127 I, as hydrological and geochemical tracers in aquatic systems, a new high performance liquid chromatography (HPLC) method was developed for the determination of iodine speciation. The dissolved iodine species that dominate natural water systems are iodide, iodate, and organic iodine. Using this new method, iodide was determined directly by combining anion exchange chromatography and spectrophotometry. Iodate and the total of organic iodine species are determined as iodide, with minimal sample preparation, compared to existing methods. The method has been applied to quantitatively determine iodide, iodate as the difference of total inorganic iodide and iodide after reduction of the sample by NaHSO 3 , and organic iodine as the difference of total iodide (after organic decomposition by dehydrohalogenation and reduction by NaHSO 3 ) and total inorganic iodide. Analytical accuracy was tested: (1) against certified reference material, SRM 1549, powdered milk (NIST); (2) through the method of standard additions; and (3) by comparison to values of environmental waters measured independently by inductively coupled plasma mass spectrometry (ICP-MS). The method has been successfully applied to measure the concentrations of iodide species in rain, surface and ground water, estuarine and seawater samples. The detection limit was ∼1 nM (0.2 ppb), with less than 3% relative standard deviation (R.S.D.) for samples determined by standard additions to an iodide solution of 20 nM in 0.1 M NaCl. This technique is one of the few methods sensitive enough to accurately quantify stable iodine species at nanomolar concentrations in aquatic systems across a range of matrices, and to quantitatively measure organic iodine. Additionally, this method makes use of a very dilute mobile phase, and may be applied to small sample volumes without pre-column concentration or post-column reactions

DETERMINATION OF THE 129I IN PRIMARY COOLANT OF PWR

Directory of Open Access Journals (Sweden)

KE CHON CHOI

2013-02-01

In this report, the effect of the boron content in a pressurized-water reactor primary coolant on the separation process of 129I was examined, as was the effect of 3H on the measurement of the activity of iodine. As a result, no influence of the boron content and of the simultaneous 3H presence was found with activity concentrations of 3H lower than 50 Bq/mL, and with a boron concentration of less than 2,000 μg/mL.

Reconstructing surface ocean circulation with 129I time series records from corals.

Science.gov (United States)

Chang, Ching-Chih; Burr, George S; Jull, A J Timothy; Russell, Joellen L; Biddulph, Dana; White, Lara; Prouty, Nancy G; Chen, Yue-Gau; Shen, Chuan-Chou; Zhou, Weijian; Lam, Doan Dinh

2016-12-01

The long-lived radionuclide 129 I (half-life: 15.7 × 10 6  yr) is well-known as a useful environmental tracer. At present, the global 129 I in surface water is about 1-2 orders of magnitude higher than pre-1960 levels. Since the 1990s, anthropogenic 129 I produced from industrial nuclear fuels reprocessing plants has been the primary source of 129 I in marine surface waters of the Atlantic and around the globe. Here we present four coral 129 I time series records from: 1) Con Dao and 2) Xisha Islands, the South China Sea, 3) Rabaul, Papua New Guinea and 4) Guam. The Con Dao coral 129 I record features a sudden increase in 129 I in 1959. The Xisha coral shows similar peak values for 129 I as the Con Dao coral, punctuated by distinct low values, likely due to the upwelling in the central South China Sea. The Rabaul coral features much more gradual 129 I increases in the 1970s, similar to a published record from the Solomon Islands. The Guam coral 129 I record contains the largest measured values for any site, with two large peaks, in 1955 and 1959. Nuclear weapons testing was the primary 129 I source in the Western Pacific in the latter part of the 20th Century, notably from testing in the Marshall Islands. The Guam 1955 peak and Con Dao 1959 increases are likely from the 1954 Castle Bravo test, and the Operation Hardtack I test is the most likely source of the 1959 peak observed at Guam. Radiogenic iodine found in coral was carried primarily through surface ocean currents. The coral 129 I time series data provide a broad picture of the surface distribution and depth penetration of 129 I in the Pacific Ocean over the past 60 years. Copyright © 2016 The Authors. Published by Elsevier Ltd.. All rights reserved.

¹²⁹I and ¹³⁷Cs in groundwater in the vicinity of Fukushima Dai-ichi nuclear power plant

DEFF Research Database (Denmark)

Xu, Sheng; Zhang, Luyuan; Freeman, Stewart P.H.T.

2016-01-01

. The minimal 129I/137Cs activity ratios in the groundwater are more than 2–500 times higher than the FDNPP source ratio. These data can be explained by rainwater infiltrating through the surface soils, with the more water-soluble 129I preferentially extracted into the aqueous phase and the 137Cs preferentially......This paper reports iodine (127I and 129I) and cesium (137Cs) isotope concentrations in groundwater of confined and unconfined aquifers in the vicinity of the Fukushima Dai-ichi nuclear power plant (FDNPP). 127I and 129I concentrations range from 2–13 μg/L and 5 × 107–8 × 1010 atom/L respectively...... retained in the soil....

Age and speciation of iodine in groundwater and mudstones of the Horonobe area, Hokkaido, Japan: Implications for the origin and migration of iodine during basin evolution

Science.gov (United States)

Togo, Yoko S.; Takahashi, Yoshio; Amano, Yuki; Matsuzaki, Hiroyuki; Suzuki, Yohey; Terada, Yasuko; Muramatsu, Yasuyuki; Ito, Kazumasa; Iwatsuki, Teruki

2016-10-01

This paper reports the concentration, speciation and isotope ratio (129I/127I) of iodine from both groundwater and host rocks in the Horonobe area, northern Hokkaido, Japan, to clarify the origin and migration of iodine in sedimentary rocks. Cretaceous to Quaternary sedimentary rocks deposited nearly horizontally in Tenpoku Basin and in the Horonobe area were uplifted above sea level during active tectonics to form folds and faults in the Quaternary. Samples were collected from the Pliocene Koetoi and late Miocene Wakkanai formations (Fms), which include diatomaceous and siliceous mudstones. The iodine concentration in groundwater, up to 270 μmol/L, is significantly higher than that of seawater, with the iodine enrichment factor relative to seawater reaching 800-1500. The iodine concentration in the rocks decreases from the Koetoi to Wakkanai Fms, suggesting that iodine was released into the water from the rocks of deeper formations. The iodine concentration in the rocks is sufficiently high for forming iodine-rich groundwater as found in this area. X-ray absorption near edge structure (XANES) analysis shows that iodine exists as organic iodine and iodide (I-) in host rocks, whereas it exists mainly as I- in groundwater. The isotope ratio is nearly constant for iodine in the groundwater, at [0.11-0.23] × 10-12, and it is higher for iodine in rocks, at [0.29-1.1] × 10-12, giving iodine ages of 42-60 Ma and 7-38 Ma, respectively. Some iodine in groundwater must have originated from Paleogene and even late Cretaceous Fms, which are also considered as possible sources of oil and gas, in view of the old iodine ages of the groundwater. The iodine ages of the rocks are older than the depositional ages, implying that the rocks adsorbed some iodine from groundwater, which was sourced from greater depths. The iodine concentration in groundwater decreases with decreasing chlorine concentration due to mixing of iodine-rich connate water and meteoric water. A likely scenario

Iodine status in pregnancy: role of dietary habits and geographical origin.

Science.gov (United States)

Mian, Caterina; Vitaliano, Pantaleo; Pozza, Dina; Barollo, Susi; Pitton, Mariangela; Callegari, Giovanna; Di Gianantonio, Elena; Casaro, Anna; Nacamulli, Davide; Busnardo, Benedetto; Mantero, Franco; Girelli, Maria Elisa

2009-05-01

A study was conducted on iodine status during pregnancy and its dependence on dietary habits, racial and geographical origin, and time since arrival in Italy. We enrolled 322 consecutive pregnant women: 217 Italians, 62 Eastern Europeans and 43 from Northern and Central Africa. All women completed a food frequency questionnaire on their dietary habits. The urinary iodide concentration (UIC) was determined in spot morning urine samples. In the group as a whole, the median UIC was 83 microg/l; the UIC was Iodine supplements were used by 40% of the women, and UIC were higher in those who did so than in those who did not (median 103 vs. 75 microg/l, P = 0.03), particularly if the latter did not drink milk (median 98 vs. 42 microg/l, P = 0.01). Multivariate analysis showed that milk was the only variable influencing UIC (OR 1.29, P = 0.0005). (i) Iodine levels are too low among pregnant women in our region, and particularly in foreign women. (ii) Cow's milk intake is their main source of iodine. (iii) Iodine supplementation is mandatory during pregnancy, particularly for women do not drink milk.

Serum thyroglobulin and urinary iodine concentration are the most appropriate indicators of iodine status and thyroid function under conditions of increasing iodine supply in schoolchildren in Benin

NARCIS (Netherlands)

van den Briel, T.; West, C. E.; Hautvast, J. G.; Vulsma, T.; de Vijlder, J. J.; Ategbo, E. A.

2001-01-01

Iodine deficiency control programs have greatly reduced iodine deficiency disorders worldwide. For monitoring changes in iodine status, different indicators may be used. The aim of this study was to evaluate the suitability of indicators of iodine status and thyroid function, thyroglobulin (Tg),

An investigation of the potential uses of iodine monochloride as a titrant in thermometric titrimetry.

Science.gov (United States)

Bark, L S; Grime, J K

An investigation has been made of the potential uses of iodine monochloride as a titrant in thermometric titrimetry. A series of substances, inorganic and organic, has been selected so that a range of stoichiometries and of various types of reaction products result from the oxidation. It has been found to be necessary to prevent the formation of iodine formed by oxidation of the iodide produced by the reduction of iodine monochloride. This is successfully accomplished by using mercury(II) to mask the iodide in a mercury(II)-iodide complex. However, the evolution of gaseous products tends to give curvature of the enthalpogram near the equivalence point and the method is not recommended for the determination of compounds such as thiosemicarbazide. For many other systems, iodine monochloride used in the presence of mercury(II) has analytical potential as a thermometric titrant.

Migration chemistry and behaviour of iodine relevant to geological disposal of radioactive wastes. A literature review with a compilation of sorption data

International Nuclear Information System (INIS)

Liu, Y.; Gunten, H.R. von

1988-09-01

This report reviews the literature on iodine migration, chemistry and behaviour in the environment up to November 1987. It deals mainly with 129 I released from a land repository, with particular consideration of the Swiss scenario for the disposal of low- and medium-level radioactive waste. As a background to this review, the basic properties of radioiodine, its distribution, circulation in nature and radiological impact are presented. A large number of sorption and diffusion data for iodine on rocks, sediments, minerals, cements and other materials have been compiled from many different laboratories. Based on this information, an assessment of the sorption and retardation of radioiodine in geomedia is made and methodologies for obtaining sorption distribution ratios (R D values) are discussed. The review also covers natural analogue studies of 129 I, retardation of iodine by cement barriers and the possible influences of organic compounds and microorganisms on the behaviour of iodine. Some possibilities for further research on diffusion measurements and near-field chemistry of radioiodine are outlined. (author) 259 refs., 9 figs., 32 tabs

Water Circulation and Marine Environment in the Antarctic Traced by Speciation of ¹²⁹I and ¹²⁷I

DEFF Research Database (Denmark)

Xing, Shan; Hou, Xiaolin; Aldahan, Ala

2017-01-01

Emissions of anthropogenic 129I from human nuclear activities are now detected in the surface water of the Antarctic seas. Surface seawater samples from the Drake Passage, Bellingshausen, Amundsen, and Ross Seas were analyzed for total 129I and 127I, as well as for iodide and iodate of these two....... The iodine distribution patterns provide useful information on surface water transport and mixing that are vital for better understanding of the Southern Oceans effects on the global climate change. The results indicate multiple spatial interactions between the Antarctic Circumpolar Current (ACC......) and Antarctic Peninsula Coastal Current (APCC). These interactions happen in restricted circulation pathways that may partly relate to glacial melting and icebergs transport. Biological activity during the warm season should be one of the key factors controlling the reduction of iodate in the coastal water...

Carbon, cesium and iodine isotopes in Japanese cedar leaves from Iwaki, Fukushima

DEFF Research Database (Denmark)

Xu, Sheng; Cook, Gordon T.; Cresswell, Alan J.

2016-01-01

Japanese cedar leaves from Iwaki, Fukushima were analyzed for carbon, cesium and iodine isotopic compositions before and after the 2011 nuclear accident. The Δ14C values reflect ambient atmospheric 14C concentrations during the year the leaves were sampled/defoliated, and also previous year......(s). The elevated 129I and 134,137Cs concentrations are attributed to direct exposure to the radioactive fallout for the pre-fallout-expended leaves and to internal translocation from older parts of the tree for post-fallout-expended leaves. 134Cs/137Cs and 129I/137Cs activity ratios suggest insignificant isotopic...

Automatic Method for Controlling the Iodine Adsorption Number in Carbon Black Oil Furnaces

Directory of Open Access Journals (Sweden)

Zečević, N.

2008-12-01

Full Text Available There are numerous of different inlet process factors in carbon black oil furnaces which must be continuously and automatically adjusted, due to stable quality of final product. The most important six inlet process factors in carbon black oil-furnaces are:1. volume flow of process air for combustion2. temperature of process air for combustion3. volume flow of natural gas for insurance the necessary heat for thermal reaction of conversionthe hydrocarbon oil feedstock in oil-furnace carbon black4. mass flow rate of hydrocarbon oil feedstock5. type and quantity of additive for adjustment the structure of oil-furnace carbon black6. quantity and position of the quench water for cooling the reaction of oil-furnace carbon black.The control of oil-furnace carbon black adsorption capacity is made with mass flow rate of hydrocarbon feedstock, which is the most important inlet process factor. Oil-furnace carbon black adsorption capacity in industrial process is determined with laboratory analyze of iodine adsorption number. It is shown continuously and automatically method for controlling iodine adsorption number in carbon black oil-furnaces to get as much as possible efficient control of adsorption capacity. In the proposed method it can be seen the correlation between qualitatively-quantitatively composition of the process tail gasses in the production of oil-furnace carbon black and relationship between air for combustion and hydrocarbon feedstock. It is shown that the ratio between air for combustion and hydrocarbon oil feedstock is depended of adsorption capacity summarized by iodine adsorption number, regarding to BMCI index of hydrocarbon oil feedstock.The mentioned correlation can be seen through the figures from 1. to 4. From the whole composition of the process tail gasses the best correlation for continuously and automatically control of iodine adsorption number is show the volume fraction of methane. The volume fraction of methane in the

Removal efficiency of silver impregnated filter materials and performance of iodie filters in the off-gas of the Karlsruhe reprocessing plant WAK

International Nuclear Information System (INIS)

Herrmann, F.J.; Herrmann, B.; Hoeflich, V.

1997-01-01

An almost quantitative retention of iodine is required in reprocessing plants. For the iodine removal in the off-gas streams of a reprocessing plant various sorption materials had been tested under realistic conditions in the Karlsruhe reprocessing plant WAK in cooperation with the Karlsruhe research center FZK. The laboratory results achieved with different iodine sorption materials justified long time performance tests in the WAK Plant. Technical iodine filters and sorption materials for measurements of iodine had been tested from 1972 through 1992. This paper gives an overview over the most important results, Extended laboratory, pilot plant, hot cell and plant experiences have been performed concerning the behavior and the distribution of iodine-129 in chemical processing plants. In a conventional reprocessing plant for power reactor fuel, the bulk of iodine-129 and iodine-127 is evolved into the dissolver off-gas. The remainder is dispersed over many aqueous, organic and gaseous process and waste streams of the plant. Iodine filters with silver nitrate impregnated silica were installed in the dissolver off-gas of the Karlsruhe reprocessing plant WAK in 1975 and in two vessel vent systems in 1988. The aim of the Karlsruhe iodine research program was an almost quantitative evolution of the iodine during the dissolution process to remove as much iodine with the solid bed filters as possible. After shut down of the WAK plant in December 1990 the removal efficiency of the iodine filters at low iodine concentrations had been investigated during the following years. 12 refs., 2 figs., 2 tabs

Removal efficiency of silver impregnated filter materials and performance of iodie filters in the off-gas of the Karlsruhe reprocessing plant WAK

Energy Technology Data Exchange (ETDEWEB)

Herrmann, F.J.; Herrmann, B.; Hoeflich, V. [Wiederaufarbeitungsanlage Karlsruhe (Germany)] [and others

1997-08-01

An almost quantitative retention of iodine is required in reprocessing plants. For the iodine removal in the off-gas streams of a reprocessing plant various sorption materials had been tested under realistic conditions in the Karlsruhe reprocessing plant WAK in cooperation with the Karlsruhe research center FZK. The laboratory results achieved with different iodine sorption materials justified long time performance tests in the WAK Plant. Technical iodine filters and sorption materials for measurements of iodine had been tested from 1972 through 1992. This paper gives an overview over the most important results, Extended laboratory, pilot plant, hot cell and plant experiences have been performed concerning the behavior and the distribution of iodine-129 in chemical processing plants. In a conventional reprocessing plant for power reactor fuel, the bulk of iodine-129 and iodine-127 is evolved into the dissolver off-gas. The remainder is dispersed over many aqueous, organic and gaseous process and waste streams of the plant. Iodine filters with silver nitrate impregnated silica were installed in the dissolver off-gas of the Karlsruhe reprocessing plant WAK in 1975 and in two vessel vent systems in 1988. The aim of the Karlsruhe iodine research program was an almost quantitative evolution of the iodine during the dissolution process to remove as much iodine with the solid bed filters as possible. After shut down of the WAK plant in December 1990 the removal efficiency of the iodine filters at low iodine concentrations had been investigated during the following years. 12 refs., 2 figs., 2 tabs.

Measurement of thyroid volume, iodine concentration and total iodine content by CT and its clinical significance

International Nuclear Information System (INIS)

Nakaji, Shunsuke; Imanishi, Yoshimasa; Okamoto, Kyouko; Shinagawa, Toshihito

2007-01-01

Recently, Imanishi et al have developed new CT software for quantitative in vivo measurement of thyroid iodine. Using a CT system with the software, we measured volume, iodine concentration and total iodine content of thyroids in 63 controls and 435 patients with various diffuse thyroid diseases and thyroid nodules. In controls, all of them showed no difference between the sexes. Although the iodine concentration of the thyroid showed no difference among children, adults and seniles, the volume and total iodine content of the thyroid appeared smaller in children and seniles than in adults. In addition, although the volume and iodine concentration of the thyroid had two peaks in distribution, the total iodine content had almost normal distribution. Normal range of volume, iodine concentration and total iodine content in adults were 5.2-15.5 cm 3 , 0.28831-0.85919 mg/cm 3 and 2.35-11.69 mg, respectively. In thyroid nodule, there is no significant difference in volume, iodine concentration and total iodine content between benign and malignant nodules. All nodules with iodine concentration of less than 0.00007 mg/cm 3 were benign. No thyroid was higher in iodine concentration than the normal range although the thyroid was lower in 78.7% of patients with diffuse thyroid diseases. In all thyroids with increasing iodine concentration and total iodine content in medication course, thyroidal symptoms and signs were uncontrollable by the medication. In 43.8% of patients with long-period systemic diseases, the thyroid showed abnormality in any of the three. We concluded that quantitative in vivo measurement of thyroid iodine by CT could assist the diagnosis of thyroid diseases and decision of therapeutic methods. (author)

Multi-compartment iodine calculations with FIPLOC/IMPAIR

Energy Technology Data Exchange (ETDEWEB)

Ewig, F; Allelein, H J [Gesellschaft fuer Anlagen- und Reaktorsicherheit mbH (GRS), Koeln (Germany); Schwarz, S; Weber, G [Gesellschaft fuer Anlagen- und Reaktorsicherheit (GRS) mbH, Garching (Germany)

1996-12-01

The multi-compartment containment code FIPLOC for the simulation of severe accidents in LWR plants was extended by the integration of the iodine model IMPAIR-3. The iodine model was changed for arbitrary compartment configurations and tightly coupled to the thermal hydraulic part. A main progress with the coupled version FIPLOC-3.0 is the sophisticated modelling of the aerosol iodine behaviour. In a PWR accident the mass of iodine is mainly released in form of CsI aerosol from the primary circuit. In IMPAIR-3 the aerosol behaviour of the species CsI, AgI and IO{sub 3}{sup -} is modelled in a very simplified way causing large uncertainties in the calculated distributions. The behaviour of these three aerosol species is treated by the aerosol model MAEROS/MGA. Agglomeration, particle growth by condensation and all deposition processes are calculated. The solubility effect for the hygroscopic species CsI and IO{sub 3}{sup -} are comprehended. Furthermore the impact of the iodine decay heat on the thermal hydraulic behaviour is considered. In order to test the code development a preliminary FIPLOC-3.0 calculation was done simulating a German PWR containment for the core melt scenario ND* according to the German risk study phase B. IN the calculation a contact of the core melt with the sump water was assumed and the containment vent line was opened after 70 hours. The result show that the different iodine species are distributed inhomogeneously within the containment. The CsI-aerosol concentrations differ by two orders of magnitude and the I{sub 2}-concentration even by three orders of magnitude. Most of the iodine is assumed to be released as CsI aerosol out of the primary circuit. Since it fastly deposits its contribution to the release into the environment is minor. CsI is however dissolved in the sump, where mainly the gaseous I{sub 2} is created which can react in the containment atmosphere to IO{sub 3}{sup -}. (author) 11 figs., 3 tabs., 12 refs.

Multi-compartment iodine calculations with FIPLOC/IMPAIR

International Nuclear Information System (INIS)

Ewig, F.; Allelein, H.J.; Schwarz, S.; Weber, G.

1996-01-01

The multi-compartment containment code FIPLOC for the simulation of severe accidents in LWR plants was extended by the integration of the iodine model IMPAIR-3. The iodine model which originally was only drafted for chains of compartments was changed for arbitrary compartment configurations and tightly coupled to the thermal hydraulic part. A main progress with the coupled version FIPLOC-3.0 is the sophisticated modelling of the aerosol iodine behaviour. In a PWR accident the mass of iodine is mainly released in form of CsI aerosol from the primary circuit. In IMPAIR-3 the aerosol behaviour of the species CsI, AgI and IO 3 - is modelled in a very simplified way causing large uncertainties in the calculated distributions. The behaviour of these three aerosol species is treated by the aerosol model MAEROS/MGA. Agglomeration, particle growth by condensation and all deposition processes are calculated. The solubility effect for the hygroscopic species CsI and IO 3 - are comprehended. Furthermore the impact of the iodine decay heat on the thermal hydraulic behaviour is considered. In order to test the code development a preliminary FIPLOC-3.0 calculation was done simulating a German PWR containment for the core melt scenario ND* according to the German risk study phase B. IN the calculation a contact of the core melt with the sump water was assumed and the containment vent line was opened after 70 hours. The result show that the different iodine species are distributed inhomogeneously within the containment. The CsI-aerosol concentrations differ by two orders of magnitude and the I 2 -concentration even by three orders of magnitude. Most of the iodine is assumed to be released as CsI aerosol out of the primary circuit. Since it fastly deposits its contribution to the release into the environment is minor. CsI is however dissolved in the sump, where mainly the gaseous I 2 is created which can react in the containment atmosphere to IO 3 - . (author) 11 figs., 3 tabs., 12

Novel molecular-level evidence of iodine binding to natural organic matter from Fourier transform ion cyclotron resonance mass spectrometry

Energy Technology Data Exchange (ETDEWEB)

Xu, Chen, E-mail: xuchen66@tamu.edu [Laboratory for Environmental and Oceanographic Research, Department of Marine Sciences, Texas A and M University, Building 3029, Galveston, TX 77551 (United States); Chen, Hongmei [Department of Chemistry and Biochemistry, Old Dominion University, Norfolk, VA 23529 (United States); Sugiyama, Yuko [Department of Chemistry and Biochemistry, Old Dominion University, Norfolk, VA 23529 (United States); University of Hyogo, 1-1-12, Shinzaike-honcho, Himeji, Hyogo 670-0092 (Japan); Zhang, Saijin; Li, Hsiu-Ping; Ho, Yi-Fang; Chuang, Chia-ying; Schwehr, Kathleen A. [Laboratory for Environmental and Oceanographic Research, Department of Marine Sciences, Texas A and M University, Building 3029, Galveston, TX 77551 (United States); Kaplan, Daniel I. [Savannah River National Laboratory, Aiken, SC 29808 (United States); Yeager, Chris [Los Alamos National Laboratory, Los Alamos, NM 87545 (United States); Roberts, Kimberly A. [Savannah River National Laboratory, Aiken, SC 29808 (United States); Hatcher, Patrick G. [Department of Chemistry and Biochemistry, Old Dominion University, Norfolk, VA 23529 (United States); Santschi, Peter H. [Laboratory for Environmental and Oceanographic Research, Department of Marine Sciences, Texas A and M University, Building 3029, Galveston, TX 77551 (United States)

2013-04-01

Major fractions of radioiodine ({sup 129}I) are associated with natural organic matter (NOM) in the groundwater and surface soils of the Savannah River Site (SRS). Electrospray ionization coupled to Fourier transform ion cyclotron resonance mass spectrometry (ESI-FTICR-MS) was applied to elucidate the interactions between inorganic iodine species (iodide and iodate) and a fulvic acid (FA) extracted from a SRS surface soil. Iodate is likely reduced to reactive iodine species by the lignin- and tannin-like compounds or the carboxylic-rich alicyclic molecules (CRAM), during which condensed aromatics and lignin-like compounds were generated. Iodide is catalytically oxidized into reactive iodine species by peroxides, while FA is oxidized by peroxides into more aliphatic and less aromatic compounds. Only 9% of the total identified organo-iodine compounds derived from molecules originally present in the FA, whereas most were iodine binding to newly-produced compounds. The resulting iodinated molecules were distributed in three regions in the van Krevelen diagrams, denoting unsaturated hydrocarbons, lignin and protein. Moreover, characteristics of these organo-iodine compounds, such as their relatively low O/C ratios (< 0.2 or < 0.4) and yet some degree of un-saturation close to that of lignin, have multiple important environmental implications concerning possibly less sterically-hindered aromatic ring system for iodine to get access to and a lower hydrophilicity of the molecules thus to retard their migration in the natural aquatic systems. Lastly, ∼ 69% of the identified organo-iodine species contains nitrogen, which is presumably present as -NH{sub 2} or -HNCOR groups and a ring-activating functionality to favor the electrophilic substitution. The ESI-FTICR-MS technique provides novel evidence to better understand the reactivity and scavenging properties of NOM towards radioiodine and possible influence of NOM on {sup 129}I migration. Highlights: ► IO{sub 3}{sup �

Surface analytical investigations of the release behaviour of volatile fission products during simulated core meltdown accidents and of the reaction behaviour of iodine with silver surfaces

International Nuclear Information System (INIS)

Moers, H.

1986-07-01

The report presents the results of the analysis of aerosol particles formed in simulated laboratory scale core meltdown experiments. In addition the interaction of silver surfaces with gaseous molecular iodine and with iodide and molecular iodine in aqueous solution was investigated. The composition of the aerosol samples and the progress of the reactions mentioned were determined by use of surface analytical techniques (X-ray photoelectron spectroscopy, Auger electron spectroscopy, secondary ion mass spectroscopy). The major information can be evaluated from X-ray photoelectron spectra which exhibit chemical shifts of the photoelectron lines which allowing a discrimination between different chemical species of the same element. The analyses showed that iodine is present in the aerosol particles mainly as caesium iodide and, to a smaller fraction, as silver iodide. During the adsorption of gaseous molecular iodine at metallic silver surfaces a closed silver iodide overlayer is formed. In aqueous iodide solutions one observes chemisorption of the iodide anions up to a coverage of the metallic silver surface of about half a monolayer. Molecular iodine in aqueous solution is completely converted to silver iodide which covers the substrate irregularly. (orig./HP) [de

The management of carbon-14 and iodine-129 wastes - a site specific survey of current and future arisings, possible management options and potential impact with respect to the United Kingdom

International Nuclear Information System (INIS)

Briggs, A.

1988-06-01

Part 1 - A site-specific survey, by the Harwell Laboratory, of current and future gaseous, liquid and solid arisings of 14 C and 129 I at UK nuclear installations, is presented in the form of tables and maps. In the tables the arisings are characterised in terms of quantity, activity and accompanying radionuclides. Management options discussed are: dispersal in the environment; capture and retention of arisings from power stations, reprocessing plants, and industrial sites producing pharmaceuticals and research materials; direct disposal of unprocessed spent fuel elements in an underground repository. Comparative costings of the various options are given. Part 2 - The information in part 1 is used by the National Radiological Protection Board as the basis for an examination of the effects that various management options would have on the radiological impact of 14 C and 129 I on the public. Comparison is made between different types of discharge, and disposal as a solid waste to various kinds of repository, in terms of their health detriment costs. Emphasis is placed on illustrating the use of a decision analysis methodology for assessment of the different waste management strategies. (author)

Study on iodine levels in thyroids of iodine-supplemented rats by epithermal neutron activation analysis

International Nuclear Information System (INIS)

Wang Xuefei; Zhang Fang; Xu Qing; Liu Nianqing; Chai Zhifang; Zhao Xueqin; Zuo Aijun

2003-01-01

The second generation female Wistar rats that have been treated with iodine-deficient food, after their delivery, are divided into three groups i.e. excessive-iodine (EI), adequate-iodine (AI) and iodine-deficient (ID) according to the KIO 3 concentration in the drinking water (3.0, 0.4, 0 mg/L). In addition, the normal rats with low iodine food and 0.4 mg/L KIO 3 water are used as the control group (C). The iodine content in thyroid and the serum thyroid hormone levels of the third generation rats are measured by means of epithermal neutron activation analysis (ENAA), and the method of enzyme-linked immunosorbent assay (ELISA), respectively. The results indicate that the total thyroxine (TT 4 ) and the free thyroxine (FT 4 ) of the EI, compared with those of the controls, are significantly decreased (p 3 ) evidently increased (p 4 , FT 4 and goiter

An approach for measuring the {sup 129}I/{sup 127}I ratio in fish samples

Energy Technology Data Exchange (ETDEWEB)

Kusuno, Haruka, E-mail: kusuno@um.u-tokyo.ac.jp [The University Museum, The University of Tokyo, 3-7-1 Hongo, Bunkyo-ku, Tokyo 113-0033 (Japan); Matsuzaki, Hiroyuki [The University Museum, The University of Tokyo, 3-7-1 Hongo, Bunkyo-ku, Tokyo 113-0033 (Japan); Nagata, Toshi; Miyairi, Yosuke; Yokoyama, Yusuke [Atmosphere and Ocean Research Institute, The University of Tokyo, 5-1-5, Kashiwanoha, Kashiwa-shi, Chiba 277-8564 (Japan); Ohkouchi, Naohiko [Japan Agency for Marine-Earth Science and Technology, 2-15, Natsushima-cho, Yokosuka-city, Kanagawa 237-0061 (Japan)

2015-10-15

The {sup 129}I/{sup 127}I ratio in marine fish samples was measured employing accelerator mass spectrometry. The measurement was successful because of the low experimental background of {sup 129}I. Pyrohydrolysis was applied to extract iodine from fish samples. The experimental background of pyrohydrolysis was checked carefully and evaluated as 10{sup 4}–10{sup 5} atoms {sup 129}I/combustion. The methodology employed in the present study thus required only 0.05–0.2 g of dried fish samples. The methodology was then applied to obtain the {sup 129}I/{sup 127}I ratio of marine fish samples collected from the Western Pacific Ocean as (0.63–1.2) × 10{sup −10}. These values were similar to the ratio for the surface seawater collected at the same station, 0.4 × 10{sup −10}. The {sup 129}I/{sup 127}I ratio of IAEA-414, which was a mix of fish from the Irish Sea and the North Sea, was also measured and determined as 1.82 × 10{sup −7}. Consequently, fish from the Western Pacific Ocean and the North Sea were distinguished by their {sup 129}I/{sup 127}I ratios. The {sup 129}I/{sup 127}I ratio is thus a direct indicator of the area of habitat of fish.

CFD Analyses of Re-Evolved Iodine from an In-containment Water Pool

Energy Technology Data Exchange (ETDEWEB)

Kim, Tae Hyeon [KHNP CRI, Daejeon (Korea, Republic of); Yoon, Woo Sung; Jung, Ji Hwan [Pusan National University, Busan (Korea, Republic of)

2016-10-15

A good understanding of the behavior of iodine is required to evaluate the safety and emergency procedures after a LOCA. The quantity of re-evolved iodine is related to pH level, temperature, and iodine concentration of water pool. In the calculation of pH for water pool, sequence calculations must consider this variable if any aqueous iodine is present, even if it is initially present in stable forms. The present study consists of two parts: the pH evaluation and the evaluation of the iodine re-evolution. The current paper focuses on the pH evaluation method, the development of a user-defined function (UDF) and the iodine re-evolution from the water pool. CFD that incorporates the UDF was used in this study to calculate the local pH level in the transient condition. The amount of re-evolved iodine was calculated based on the iodine concentration, temperature, and pH. The transportation and resulting distribution of the iodine concentration, temperature, and pH were calculated using transient analyses with CFD. The quantity of reevolved iodine was obtained with several assumptions. The quantitative evaluation of re-evolved iodine during a LOCA in a commercial nuclear power plants is done in two stages. The first stage is to calculate the pH in the water pool, and the second stage is to calculate the quantity of re-evolved iodine. Evaporated iodine, from the water pool water to the containment atmosphere, can be estimated from characteristic iodine behaviors and pH calculations. The 3D CFD analysis results show that the pH reached 7.0 after 149.5 minutes. Near the spillway, the change in averaged pH was faster than the change in wholevolume averaged pH. Evaluating the amount of reevolved iodine were examined using four different methods. As a result of our evaluation of iodine reevolution, the initial molecular iodine concentration of a water pool has a significant impact on the amount of gaseous iodine, more so than the pH or temperature, due to the locally similar

CFD Analyses of Re-Evolved Iodine from an In-containment Water Pool

International Nuclear Information System (INIS)

Kim, Tae Hyeon; Yoon, Woo Sung; Jung, Ji Hwan

2016-01-01

A good understanding of the behavior of iodine is required to evaluate the safety and emergency procedures after a LOCA. The quantity of re-evolved iodine is related to pH level, temperature, and iodine concentration of water pool. In the calculation of pH for water pool, sequence calculations must consider this variable if any aqueous iodine is present, even if it is initially present in stable forms. The present study consists of two parts: the pH evaluation and the evaluation of the iodine re-evolution. The current paper focuses on the pH evaluation method, the development of a user-defined function (UDF) and the iodine re-evolution from the water pool. CFD that incorporates the UDF was used in this study to calculate the local pH level in the transient condition. The amount of re-evolved iodine was calculated based on the iodine concentration, temperature, and pH. The transportation and resulting distribution of the iodine concentration, temperature, and pH were calculated using transient analyses with CFD. The quantity of reevolved iodine was obtained with several assumptions. The quantitative evaluation of re-evolved iodine during a LOCA in a commercial nuclear power plants is done in two stages. The first stage is to calculate the pH in the water pool, and the second stage is to calculate the quantity of re-evolved iodine. Evaporated iodine, from the water pool water to the containment atmosphere, can be estimated from characteristic iodine behaviors and pH calculations. The 3D CFD analysis results show that the pH reached 7.0 after 149.5 minutes. Near the spillway, the change in averaged pH was faster than the change in wholevolume averaged pH. Evaluating the amount of reevolved iodine were examined using four different methods. As a result of our evaluation of iodine reevolution, the initial molecular iodine concentration of a water pool has a significant impact on the amount of gaseous iodine, more so than the pH or temperature, due to the locally similar

Urinary Iodine Clearance following Iodinated Contrast Administration: A Comparison of Euthyroid and Postthyroidectomy Subjects

Directory of Open Access Journals (Sweden)

Janice D. Ho

2014-01-01

Full Text Available Purpose. To compare iodine clearance following iodinated contrast administration in thyroidectomised thyroid cancer patients and euthyroid individuals. Methods. A convenience population (6 thyroidectomised thyroid cancer patients and 7 euthyroid controls was drawn from patients referred for iodinated contrast-enhanced computed tomography (CT studies. Subjects had sequential urine samples collected up to 6 months (50 samples from the thyroidectomised and 63 samples from the euthyroid groups. t-tests and generalised estimating equations (GEE were used to test for group differences in urinary iodine creatinine ratios. Results. Groups had similar urinary iodine creatinine ratios at baseline, with a large increase 2 weeks following iodinated contrast (P=0.005. Both groups had a return of urinary iodine creatinine ratios to baseline by 4 weeks, with no significant group differences overall or at any time point. Conclusions. Thyroidectomised patients did not have a significantly different urinary iodine clearance than euthyroid individuals following administration of iodinated contrast. Both had a return of urinary iodine creatinine ratios to baseline within 4 weeks.

Iodine and selenium migration through argillaceous rocks

International Nuclear Information System (INIS)

Frasca, Benjamin

2011-01-01

Deep argillaceous formations are considered as potential host rock for high-level radioactive waste repository. Based on safety assessment calculations, active selenium ( 79 Se) and iodine ( 129 I) from high level radioactive waste might be ones of the major dose contributors due to their longevity and their anionic character. However, because of their high sensitivity to redox condition, a special attention to the oxidation state of these elements is required. A comparative study on the diffusion properties of selenium and iodine through argillaceous rocks was realized with the aim to determine the effects of both the redox conditions and the mineralogy on the migration of these two elements. For these purposes, we have studied two argillaceous rocks: Toarcian argillite from Tournemire (France) and Opalinus clay (OPA) from the Mont-Terri (Switzerland). The study of the iodide migration allowed to confirm the control on the iodide retention of both oxidized pyrite and natural organic matter. A kinetic control of the iodide sorption is also suspected. We focus the selenium study on the more oxidized species, Se(IV) and Se(VI). The Se(IV) migration is strongly dependant from oxido-reduction processes. Indeed, the Se(IV) diffusion experiments through Tournemire argillite and OPA indicated a significant reduction associated to Fe(II). The Se(VI) study evidenced a behavior dependant from the initial concentration: at the highest concentration, no significant retention was observed while the retention is significant at the lowest concentration. Furthermore, spectroscopic analyses tend to show a low Se(VI) reduction at the Fe contact. However, biotic origin cannot be excluded. (author)

Incorporation of iodine into calcium phosphates with apatitic structure

International Nuclear Information System (INIS)

Coulon, Antoine

2014-01-01

In order to avoid the release of 129 I (long-lived intermediate-level waste) in the environment, we describe a novel material incorporating iodine under the form of iodate in a calcium phosphate based hydroxyapatite. This material is prepared by two synthetic processes: a wet precipitation route followed by a spark plasma sintering and a cementitious route. A high iodine content (with a maximum incorporation rate of 10 wt.%) is reached for both processes, by incorporation of the iodate in the apatitic structure. A monolith with relative density of 88.6% was obtained after shaping of the precipitated powders by spark plasma sintering. This material reveals satisfactory leaching properties, with an initial leaching rate in pure water at 50 C of 10 -2 g.m -2 .j -1 , and a residual leaching rate at 50 C of 10 -5 g.m -2 .j -1 in underground water of potential geological repositories. All in all, this material is a potential candidate for the conditioning of radioactive iodine. (author) [fr

Capture of elemental and organic iodine from dilute gas streams by silver-exchanged mordenite

Energy Technology Data Exchange (ETDEWEB)

Bruffey, S.H.; Jubin, R.T.; Jordan, J.A. [Oak Ridge National Laboratory, 1 Bethel Valley Road, Oak Ridge, TN 37831 (United States)

2016-07-01

The treatment of off-gas streams arising from reprocessing of used nuclear fuel (UNF) is an area of active study by the U.S. Department of Energy. Such off-gas streams contain volatile fission products, including long-lived {sup 129}I. Although {sup 129}I is released into the off-gas at multiple points within the chemical reprocessing flowsheet, previous research has focused on removal from the dissolver off-gas stream (DOG). The DOG is expected to contain up to 98% of iodine in UNF at ppm levels within the stream. Other off-gas streams will also contain iodine but at substantially lower concentrations. Recent work has shown that compliance with U.S. regulations will likely require capture of iodine from these dilute streams in addition to capture from DOG. In particular, the vessel off-gas (VOG) stream is expected to contain 1-3% of the total iodine inventory at ppb concentrations. A review of literature also indicates that the speciation of iodine in the VOG stream will differ from that of the DOG, with the DOG containing primarily I{sub 2} and the VOG containing a mixture of I{sub 2} and organic iodine species. Silver-exchanged mordenite (AgZ) has been identified for use in the removal of iodine from off-gas streams. It is an effective capture material for I{sub 2} at the concentrations expected in the DOG, but little is known about its performance in gas streams that may contain both I{sub 2} and organic iodides at very dilute concentrations. The experiments to be described were designed to separately characterize the adsorption of I{sub 2} and methyl iodide on AgZ through extended duration testing. Simulated vessel off-gases containing low levels of either I{sub 2} or methyl iodide were contacted with AgZ sorbent beds for up to four months. Through the use of sorbent beds in series and varied sampling times, key parameters such as adsorption rate, decontamination factor, and performance over time could be determined for the capture of each species by AgZ. This

The treatment of iodine and chlorine chemistry in the risk assessment of deep radioactive waste disposal

International Nuclear Information System (INIS)

Jones, Michael A.

1992-01-01

The predicted contribution from 129 I, 131 I and 36 Cl to the radiological risk from a radioactive waste repository may be enhanced by the assumption of limited retardation in the near field and geosphere. However, migration of these radionuclides may be affected by their chemical speciation and retarded by a range of sorption processes. The chemical behaviour of iodine and chlorine is determined emphasizing i) aqueous speciations, ii) sorption onto inorganic substrates, and iii) the role of organic matter and microbes. Recommendations to enhance the methodology include i) consideration of aqueous speciation of iodine, both metal and organic complexes, ii) mechanistic simulation of iodine sorption by ion exchange and electrostatic/covalent adsorption, iii) simulation of enzymatically enhanced sorption of iodine and chlorine onto organic substrates, iv) enhancement of HMIP K d databases to include iodine and chlorine data for the geosphere and biosphere. A well defined programme of additional data collection, modelling studies and experimental investigations is recommended to achieve these enhancements. (author)

Absorption of airborne molecular iodine by water sprays

International Nuclear Information System (INIS)

Albert, M.F.; Wichner, R.P.; Baumgarten, P.K.

1986-01-01

A computer model, I2WASH, which accounts for the effect of hydrolysis reactions between molecular iodine and water, has been developed to predict the rate of removal of gaseous molecular iodine by water sprays. It has been shown that the hydrolysis reactions can affect the concentration driving force of mass transfer for molecular iodine absorption. Thus, factors that affect the hydrolysis kinetics, such as spray solution pH, iodine concentration, and temperature, should be considered in the design of a well-based absorption model. The described model also includes the effects of spray drop-size distribution, convective heat transfer, droplet evaporation or water condensation, decay heating, and ventilation air flow through the containment. The model was originally developed at Oak Ridge National Laboratory (ORNL) in 1985 for the Nuclear Regulatory Commission's Severe Accident Sequence Analysis program and has been improved to assist in a comprehensive probability risk assessment of the Savannah River Plant (SRP). Results obtained using the model are compared with those of the Containment Systems Experiments conducted at Pacific Northwest Laboratories (PNL) in 1970. An improvement over the earlier model is indicated at room temperatures, but accuracy decreases as the temperature rises. The decreased agreement at high temperature is partially due to an incomplete knowledge of the temperature effects on iodine hydrolysis reactions. The results of the I2WASH model for a postulated catastrophic accident at SRP show that ∼85% of the molecular iodine will be captured by the sprays at a buffered pH of 10.0, and ∼52% will be captured at a buffered pH of 7.0. The model is believed to be a significant improvement over (and more realistic than) other models

Auto-ignition control in turbocharged internal combustion engines operating with gaseous fuels

International Nuclear Information System (INIS)

Duarte, Jorge; Amador, Germán; Garcia, Jesus; Fontalvo, Armando; Vasquez Padilla, Ricardo; Sanjuan, Marco; Gonzalez Quiroga, Arturo

2014-01-01

Control strategies for auto-ignition control in turbocharged internal combustion engines operating with gaseous fuels are presented. Ambient temperature and ambient pressure are considered as the disturbing variables. A thermodynamic model for predicting temperature at the ignition point is developed, adjusted and validated with a large experimental data-set from high power turbocharged engines. Based on this model, the performance of feedback and feedforward auto-ignition control strategies is explored. A robustness and fragility analysis for the Feedback control strategies is presented. The feedforward control strategy showed the best performance however its implementation entails adding a sensor and new control logic. The proposed control strategies and the proposed thermodynamic model are useful tools for increasing the range of application of gaseous fuels with low methane number while ensuring a safe running in internal combustion engines. - Highlights: • A model for predicting temperature at the ignition point. • Robust PID, modified PID, and feedforward strategies for auto-ignition control. • λ′ were the best set of tuning equations for calculating controller parameters. • Robust PID showed significant improvements in auto-ignition control. • Feedforward control showed the best performance

IODINE REMOVAL EFFICIENCY IN NON-SUBMERGED AND SUBMERGED SELF-PRIMING VENTURI SCRUBBER

Directory of Open Access Journals (Sweden)

MAJID ALI

2013-04-01

Full Text Available The objective of this conducted research is to study the iodine removal efficiency in a self-priming venturi scrubber for submerged and non-submerged operating conditions experimentally and theoretically. The alkaline solution is used as an absorbent, which is prepared by dissolving sodium hydroxide (NaOH and sodium thiosulphate (Na2S2O3 in water to remove the gaseous iodine (I2 from the gas. Iodine removal efficiency is examined at various gas flow rates and inlet concentrations of iodine for submerged and non-submerged operating conditions. In the non-submerged venturi scrubber, only the droplets take part in iodine removal efficiency. However, in a submerged venturi scrubber condition, the iodine gas is absorbed from gas to droplets inside the venturi scrubber and from bubbles to surrounding liquid at the outlet of a venturi scrubber. Experimentally, it is observed that the iodine removal efficiency is greater in the submerged venturi scrubber as compare to a non-submerged venturi scrubber condition. The highest iodine removal efficiency of 0.99±0.001 has been achieved in a submerged self-priming venturi scrubber condition. A mathematical correlation is used to predict the theoretical iodine removal efficiency in submerged and non-submerged conditions, and it is compared against the experimental results. The Wilkinson et al. correlation is used to predict the bubble diameter theoretically whereas the Nukiyama and Tanasawa correlation is used for droplet diameter. The mass transfer coefficient for the gas phase is calculated from the Steinberger and Treybal correlation. The calculated results for a submerged venturi scrubber agree well with experimental results but underpredicts in the case of the non-submerged venturi scrubber.

Iodine Removal Efficiency in Non-Submerged and Submerged Self-Priming Venturi Scrubber

Energy Technology Data Exchange (ETDEWEB)

Ali, Majid; Yan, Changqi; Sun, Zhongning; Gu, Haifeng; Wang, Junlong; Mehboob; Khurram [Harbin Engineering Univ., Harbin (China)

2013-04-15

The objective of this conducted research is to study the iodine removal efficiency in a self-priming venturi scrubber for submerged and non-submerged operating conditions experimentally and theoretically. The alkaline solution is used as an absorbent, which is prepared by dissolving sodium hydroxide (NaOH) and sodium thiosulphate (Na{sub 2}S{sub 2}O{sub 3}) in water to remove the gaseous iodine (I{sub 2}) from the gas. Iodine removal efficiency is examined at various gas flow rates and inlet concentrations of iodine for submerged and non-submerged operating conditions. In the non-submerged venturi scrubber, only the droplets take part in iodine removal efficiency. However, in a submerged venturi scrubber condition, the iodine gas is absorbed from gas to droplets inside the venturi scrubber and from bubbles to surrounding liquid at the outlet of a venturi scrubber. Experimentally, it is observed that the iodine removal efficiency is greater in the submerged venturi scrubber as compare to a non-submerged venturi scrubber condition. The highest iodine removal efficiency of 0.99±0.001 has been achieved in a submerged self-priming venturi scrubber condition. A mathematical correlation is used to predict the theoretical iodine removal efficiency in submerged and non-submerged conditions, and it is compared against the experimental results. The Wilkinson et al. correlation is used to predict the bubble diameter theoretically whereas the Nukiyama and Tanasawa correlation is used for droplet diameter. The mass transfer coefficient for the gas phase is calculated from the Steinberger and Treybal correlation. The calculated results for a submerged venturi scrubber agree well with experimental results but underpredicts in the case of the non-submerged venturi scrubber.

Iodine Removal Efficiency in Non-Submerged and Submerged Self-Priming Venturi Scrubber

International Nuclear Information System (INIS)

Ali, Majid; Yan, Changqi; Sun, Zhongning; Gu, Haifeng; Wang, Junlong; Mehboob; Khurram

2013-01-01

The objective of this conducted research is to study the iodine removal efficiency in a self-priming venturi scrubber for submerged and non-submerged operating conditions experimentally and theoretically. The alkaline solution is used as an absorbent, which is prepared by dissolving sodium hydroxide (NaOH) and sodium thiosulphate (Na 2 S 2 O 3 ) in water to remove the gaseous iodine (I 2 ) from the gas. Iodine removal efficiency is examined at various gas flow rates and inlet concentrations of iodine for submerged and non-submerged operating conditions. In the non-submerged venturi scrubber, only the droplets take part in iodine removal efficiency. However, in a submerged venturi scrubber condition, the iodine gas is absorbed from gas to droplets inside the venturi scrubber and from bubbles to surrounding liquid at the outlet of a venturi scrubber. Experimentally, it is observed that the iodine removal efficiency is greater in the submerged venturi scrubber as compare to a non-submerged venturi scrubber condition. The highest iodine removal efficiency of 0.99±0.001 has been achieved in a submerged self-priming venturi scrubber condition. A mathematical correlation is used to predict the theoretical iodine removal efficiency in submerged and non-submerged conditions, and it is compared against the experimental results. The Wilkinson et al. correlation is used to predict the bubble diameter theoretically whereas the Nukiyama and Tanasawa correlation is used for droplet diameter. The mass transfer coefficient for the gas phase is calculated from the Steinberger and Treybal correlation. The calculated results for a submerged venturi scrubber agree well with experimental results but underpredicts in the case of the non-submerged venturi scrubber

Radioactive iodine and environmental and sanitary effects - bibliographic study and quantification

International Nuclear Information System (INIS)

Guetat, Ph.; Armand, P.; Monfort, M.; Fritsch, P.; Flury Herard, A.; Menetrier, F.; Bion, L.; Schoech, C.; Masset, S.

2004-01-01

This document is intended to a large public. It reviews the different parameters needed to evaluate the potential act o radioactive releases from the emission to public. Its objectives are to evaluate the importance of different exposure pathways and to assess efficiency of the possible interventions for large public. The main conclusions are summarised hereafter: The radioactive decay chains have to be taken into account to evaluate the iodine source term in the nuclear plants in the case of fission accidents. The physico-chemical forms of iodine are important in order to determine the released activity and deposited activity on the soil. The isotopes to be taken into account are mainly iodine 131 for radiological assessments and also iodine 133 for the nuclear reactor accidents, and the chain Tellurium-Iodine 132 when no particulate filtration exists. Iodine 129 in French reprocessing plant cannot lead to significant accidents. The dominant exposure pathways are related to the consumption of contaminated food products (vegetable, milk) for the inorganic iodine. The iodine transfer to goat and sheep milk is greater than the one to cow milk. The meat production of herbivores at field is the most sensitive. The interest to remove rapidly herbivore from pasture appears relatively clearly. The banning of consumption of local contaminated food products (vegetables and meats) may reduce by about a factor of thirteen the impact due to iodine 131. The youngest the population is, the greatest are the thyroid radiosensitivity and variability within the population. Oral administration of stable iodine limits transfers to maternal milk and foetal thyroid. Ingestion of stable iodine is complementary to consumption banning of local contaminated food products. The earliest the ingestion is, the greatest is the efficiency. 0,1 TBq of 131 iodine released at a low height involves only limited and local actions whereas the release of 10 TBq involves direct and immediate protection

Engineering Model Propellant Feed System Development for an Iodine Hall Thruster Demonstration Mission

Science.gov (United States)

Polzin, Kurt A.

2016-01-01

CUBESATS are relatively new spacecraft platforms that are typically deployed from a launch vehicle as a secondary payload, providing low-cost access to space for a wide range of end-users. These satellites are comprised of building blocks having dimensions of 10x10x10 cu cm and a mass of 1.33 kg (a 1-U size). While providing low-cost access to space, a major operational limitation is the lack of a propulsion system that can fit within a CubeSat and is capable of executing high (Delta)v maneuvers. This makes it difficult to use CubeSats on missions requiring certain types of maneuvers (i.e. formation flying, spacecraft rendezvous). Recently, work has been performed investigating the use of iodine as a propellant for Hall-effect thrusters (HETs) 2 that could subsequently be used to provide a high specific impulse path to CubeSat propulsion. 3, 4 Iodine stores as a dense solid at very low pressures, making it acceptable as a propellant on a secondary payload. It has exceptionally high ?Isp (density times specific impulse), making it an enabling technology for small satellite near-term applications and providing the potential for systems-level advantages over mid-term high power electric propulsion options. Iodine flow can also be thermally regulated, subliming at relatively low temperature (engineering model propellant feed system for iSAT (see Fig. 1). The feed system is based around an iodine propellant reservoir and two proportional control valves (PFCVs) that meter the iodine flow to the cathode and anode. The flow is split upstream of the PFCVs to both components can be fed from a common reservoir. Testing of the reservoir is reported to demonstrate that the design is capable of delivering the required propellant flow rates to operate the thruster. The tubing and reservoir are fabricated from hastelloy to resist corrosion by the heated gaseous iodine propellant. The reservoir, tubing, and PFCVs are heated to ensure the sublimed propellant will not re

Venturi purification device and its application in purification of gaseous waste of nuclear facilities

International Nuclear Information System (INIS)

Kong Jinsong; Yu Ren; Yang Huanlei

2013-01-01

The working principle of Venturi purification device and its purification of aerosol have been described. Then, taking the gaseous iodine as an example, the absorption process of insoluble gas pollutants is discussed, the calculation methods of the gas-liquid contact area, mass transfer rate and efficiency of mass transfer are educed, and the factors that affect the efficiency of mass transfer are analyzed. (authors)

Mixed-layered bismuth--oxygen--iodine materials for capture and waste disposal of radioactive iodine

Science.gov (United States)

Krumhansl, James L; Nenoff, Tina M

2015-01-06

Materials and methods of synthesizing mixed-layered bismuth oxy-iodine materials, which can be synthesized in the presence of aqueous radioactive iodine species found in caustic solutions (e.g. NaOH or KOH). This technology provides a one-step process for both iodine sequestration and storage from nuclear fuel cycles. It results in materials that will be durable for repository conditions much like those found in Waste Isolation Pilot Plant (WIPP) and estimated for Yucca Mountain (YMP). By controlled reactant concentrations, optimized compositions of these mixed-layered bismuth oxy-iodine inorganic materials are produced that have both a high iodine weight percentage and a low solubility in groundwater environments.

Mixed-layered bismuth-oxygen-iodine materials for capture and waste disposal of radioactive iodine

Science.gov (United States)

Krumhansl, James L; Nenoff, Tina M

2013-02-26

Materials and methods of synthesizing mixed-layered bismuth oxy-iodine materials, which can be synthesized in the presence of aqueous radioactive iodine species found in caustic solutions (e.g. NaOH or KOH). This technology provides a one-step process for both iodine sequestration and storage from nuclear fuel cycles. It results in materials that will be durable for repository conditions much like those found in Waste Isolation Pilot Plant (WIPP) and estimated for Yucca Mountain (YMP). By controlled reactant concentrations, optimized compositions of these mixed-layered bismuth oxy-iodine inorganic materials are produced that have both a high iodine weight percentage and a low solubility in groundwater environments.

Precise measurement of magnetic field gradients from free spin precession signals of He-3 and Xe-129 magnetometers

NARCIS (Netherlands)

Allmendinger, Fabian; Blümler, Peter; Doll, Michael; Grasdijk, Oliver; Heil, Werner; Jungmann, Klaus; Karpuk, Sergej; Krause, Hans-Joachim; Offenhäuser, Andreas; Repetto, Maricel; Schmidt, Ulrich; Sobolev, Yuri; Tullney, Kathlyne; Willmann, Lorenz; Zimmer, Stefan

2017-01-01

We report on precise measurements of magnetic field gradients extracted from transverse relaxation rates of precessing spin samples. The experimental approach is based on the free precession of gaseous, nuclear spin polarized He-3 and (12)9Xe atoms in a spherical cell inside a magnetic guiding field

Iodine capture by Hofmann-type clathrate Ni(II)(pz)[Ni(II)(CN)_4

International Nuclear Information System (INIS)

Massasso, Giovanni; Long, Jerome; Haines, Julien; Devautour-Vinot, Sabine; Maurin, Guillaume; Larionova, Joulia; Guerin, Christian; Guari, Yannick; Grandjean, Agnes; Onida, Barbara; Donnadieu, Bruno

2014-01-01

The thermally stable Hofmann-type clathrate framework Ni(II)(pz)[Ni(II)(CN)_4] (pz = pyrazine) was investigated for the efficient and reversible sorption of iodine (I_2) in the gaseous phase and in solution with a maximum adsorption capacity of 1 mol of I_2 per 1 mol of Ni(II)pz)[Ni(II)(CN)_4] in solution. (authors)

Treatment of gaseous and airborne radioactive waste

International Nuclear Information System (INIS)

Leichsenring, C.H.

1982-01-01

Gaseous and airborne radionuclides in the fuel cycle are retained in vessel off-gas filter systems and in the dissolver off-gas cleaning system. Those systems have to meet the regulatory requirements for both normal and accident conditions. From the solutions liquid aerosols are formed during liquid transfer (air lifts, steam jets) or by air sparging or by evaporation processes. During dissolution the volatile radionuclides i.e. 85 Kr, 129 I and 14 C are liberated and enter into the dissolver off-gas cleaning system. Flow sheets of different cleaning systems and their stage of development are described. (orig./RW)

Measurements and analysis of the 127I and 129I neutron capture and total cross sections

International Nuclear Information System (INIS)

Noguere, G.

2005-01-01

Most of the experimental work on the interaction of neutrons with matter has focused on materials important to reactor physics and reactor structures. By comparison, the corresponding data for minor actinides or long-lived fission products are poor. A significant demand has developed for improved neutron cross-section data of these little-studied nuclides due to the surge of interest in the transmutation of nuclear waste. With 400 kg of 129 I produced yearly in the reactors of the EU countries and a very long β - half-life of 1.57 x 10 7 years, iodine requires disposal strategies that will isolate this isotope from the environment for long periods of time. Therefore, 129 I is potentially a key long-lived fission product for transmutation applications, since 129 I transmutes in 130 I after a single neutron capture and decays to 130 Xe with a 12.36 h half-life. Accurate capture cross sections would help to reduce uncertainties in waste management concepts. For that purpose, Time-Of-Flight measurements covering the [0.5 eV-100 keV] energy range have been carried out at the 150 MeV pulsed neutron source GELINA of the Institute for Reference Materials and Measurements (IRMM). Two types of experiments have been performed at the IRMM, namely capture and transmission experiments. They are respectively related to the neutron capture and total cross sections. Since the PbI 2 samples used in this work contain natural and radioactive iodine, extensive measurements of 129 I have been carried out under the same experimental conditions as for the 129 I. The data reduction process was performed with the AGS system, and the resonance parameters were extracted with the SAMMY and REFIT shape analysis codes. In a last step, the parameters have been converted into ENDF-6 format and processed with the NJOY code to produce point-wise and multigroup cross sections, as well as MCNP and ERANOS libraries. (author)

Nuclear ventilation installations. Method of control of the scrubbing coefficient of iodine trap

International Nuclear Information System (INIS)

1982-12-01

The present standard aims at defining a method to control the scrubbing coefficient of radioactive iodine trapping systems, used in nuclear ventilation installations. It applies to the installations where the trapping, efficiency of radioactive iodine has to be known, tested and compared to a reference value generally included in the safety reports. It applies to the installations where the absolute pressure of the air in the ventilation systems is above 1,4. 10 5 Pa (1,4 Bar) [fr

A 60-year record of 129I in Taal Lake sediments (Philippines): Influence of human nuclear activities at low latitude region

DEFF Research Database (Denmark)

Zhang, Luyuan; Hou, Xiaolin; Li, Hong-chun

2017-01-01

in the Taal Lake core appears to be the signal of the Chernobyl accident in 1986. In addition, volcanic activities are reflected in the iodine isotope profiles in the sediment core, suggesting the potential of using iodine isotopes as an indicator of volcanic eruptions.......The influence of human nuclear activities on environmental radioactivity is not well known at low latitude region that are distant from nuclear tests sites and nuclear facilities. A sediment core collected from Taal Lake in the central Philippines was analyzed for 129I and 127I to investigate...

Balance and behavior of gaseous radionuclides released during initial fast reactor fuel reprocessing operations

International Nuclear Information System (INIS)

Leudet, A.; Goumondy, J.P.; Charrier, G.

1985-10-01

Five pins from the fast reactor Phenix are cut and dissolved in a specially designed cell for the accurate determination of gas released during the operation. Amount and activity of gaseous radionuclides: Kr, Xe, Kr-85, I, I-129, H-3 and C-14 are determined in the fuel pins and also their distribution between shearing and dissolution [fr

Probing the regional distribution of pulmonary gas exchange through single-breath gas- and dissolved-phase 129Xe MR imaging.

Science.gov (United States)

Kaushik, S Sivaram; Freeman, Matthew S; Cleveland, Zackary I; Davies, John; Stiles, Jane; Virgincar, Rohan S; Robertson, Scott H; He, Mu; Kelly, Kevin T; Foster, W Michael; McAdams, H Page; Driehuys, Bastiaan

2013-09-01

Although some central aspects of pulmonary function (ventilation and perfusion) are known to be heterogeneous, the distribution of diffusive gas exchange remains poorly characterized. A solution is offered by hyperpolarized 129Xe magnetic resonance (MR) imaging, because this gas can be separately detected in the lung's air spaces and dissolved in its tissues. Early dissolved-phase 129Xe images exhibited intensity gradients that favored the dependent lung. To quantitatively corroborate this finding, we developed an interleaved, three-dimensional radial sequence to image the gaseous and dissolved 129Xe distributions in the same breath. These images were normalized and divided to calculate "129Xe gas-transfer" maps. We hypothesized that, for healthy volunteers, 129Xe gas-transfer maps would retain the previously observed posture-dependent gradients. This was tested in nine subjects: when the subjects were supine, 129Xe gas transfer exhibited a posterior-anterior gradient of -2.00 ± 0.74%/cm; when the subjects were prone, the gradient reversed to 1.94 ± 1.14%/cm (P exchange caused by differences in lung inflation and posture.

Dissolution off-gases at the marcoule pilot facility: Iodine trapping and off-gas characterization unit

International Nuclear Information System (INIS)

Pouyat, D.; Vignau, B.; Roux, J.P.

1993-01-01

The Marcoule Pilot Reprocessing Facility (APM) reprocesses spent fuel from light water reactors and fast breeder reactors. A batch dissolution process is used with an annual throughput capacity of 5 metric tons. The off-gas treatment unit is described together with its characterization laboratory in order to highlight the functions and potential of the facilities. The objectives are consistent with the Marcoule site policy regarding diminished iodine release and investigation of the off-gas treatment process. The equipment used to meet these objectives is described from a functional standpoint. The facility implements measurement techniques to allow continuous quantitative measurements of nitrogen oxides, oxygen, iodine and krypton, as well as continuous monitoring of the demister inlet flow by γ spectrometry. Sorbents used for iodine trapping may be tested over a wide range of operating conditions (temperature, flow rate, iodine concentration) with representative dissolution off-gases. An X-ray and γ counting system is used to assess the activity of the adsorbed radionuclides, notably 129 I

Milestone Report - M3FT-15OR03120213 - A Literature Survey to Identify Potentially Problematic Volatile Iodine-Bearing Species Present in Off-Gas Streams

Energy Technology Data Exchange (ETDEWEB)

Riley, Brian [Pacific Northwest National Lab. (PNNL), Richland, WA (United States); Soelberg, Nick [Idaho National Lab. (INL), Idaho Falls, ID (United States); Jubin, Robert Thomas [Oak Ridge National Lab. (ORNL), Oak Ridge, TN (United States); Bruffey, Stephanie H. [Oak Ridge National Lab. (ORNL), Oak Ridge, TN (United States); Strachan, Denis M. [Oak Ridge National Lab. (ORNL), Oak Ridge, TN (United States)

2015-06-30

Four radionuclides have been identified as being sufficiently volatile in the reprocessing of nuclear fuel that their gaseous release needs to be controlled to meet U.S. regulatory requirements (Jubin et al. 2011, 2012). These radionuclides are ³H, ¹⁴C, ⁸⁵Kr, and ¹²⁹I. Of these, ¹²⁹I has the longest half-life and potentially highest biological impact. Accordingly, control of the release of ¹²⁹I is most critical with respect to U.S. regulations for the release of radioactive material in stack emissions. Current U.S. Environmental Protection Agency regulation governing nuclear facilities (40 CFR 190) states that the total quantity of radioactive materials entering the general environment from the entire uranium fuel cycle, per gigawatt-year of electrical energy produced by the fuel cycle, must contain less than 5 mCi of ¹²⁹I. The study of inorganic iodide in off-gas systems has been almost exclusively limited to I₂, and the focus of organic iodide studies has been CH₃I.

Aerosol and iodine removal from the head-end offgas of a reprocessing facility

International Nuclear Information System (INIS)

Furrer, J.; Wilhelm, J.C.

The offgases of a reprocessing facility must be cleaned, removing liquid and solid suspended matter, gaseous iodine and ruthenium (in the form of RuO 4 ), and the noble gases and tritium. Suspended particulates which call for radiation protection are those radioisotopes like the actinides Pu, Am, and Cm, and other radioisotopes such as 134 Cs, 137 Cs, 89 Sr, 90 Sr and 144 Ce

Compatibility of technologies with regulations in the waste management of H-3, I-129, C-14, and Kr-85. Part II. Analysis

International Nuclear Information System (INIS)

Trevorrow, L.E.; Kolba, V.M.; Vandegrift, G.F.; Steindler, M.J.

1983-11-01

Waste forms of 3 H, 129 I, 14 C, and 85 Kr separated from fuel reprocessing streams and procedures for managing them were analyzed regarding compliance with regulations. Transportation of these wastes in certain DOT-specification packagings would be permissible, but some of these packagings may not be acceptable in some disposal situations. Transportation of gaseous 85 Kr in a currently certified cylinder is possible, but a fuel reprocessor may wish to ship larger quantities per package. Disposal of tritium using a package designed by a DOE contractor and shallow land burial, in accord with the regulations of 10 CFR 61, seems practicable. Although 10 CFR 61 permits shallow land burial of 129 I, the concentration limit requires distribution in a volume that may seem impractical to commercial fuel reprocessors. The concentration limit of 10 CFR 61 for shallow land burial of 14 C requires distribution in a lesser, although still large, volume. For both 129 I and 14 C, management as high-level waste offers the advantage of smaller volumes. Similar advantages may be offered by greater confinement or non-near surface concepts for disposal. The concrete waste forms developed for these nuclides may not meet technical criteria being formulated for geologic disposal. The lack of accommodation of 85 Kr at disposal facilities makes storage of the gaseous form at the fuel reprocessing plant, followed by dispersal after partial decay, seem attractive. Ocean disposal of 129 I and 14 C by the rules of the International Atomic Energy Agency-London Ocean Dumping Convention offers advantages over shallow land burial: higher allowed concentrations, resulting in smaller volumes and fewer packages. These rules, however, thwart ocean disposal of 85 Kr since gaseous forms are banned, and for solid forms, concentration limits would require distribution of radioactivity in very large volumes. 80 references

Systematic review using meta-analyses to estimate dose-response relationships between iodine intake and biomarkers of iodine status in different population groups.

Science.gov (United States)

Ristić-Medić, Danijela; Dullemeijer, Carla; Tepsić, Jasna; Petrović-Oggiano, Gordana; Popović, Tamara; Arsić, Aleksandra; Glibetić, Marija; Souverein, Olga W; Collings, Rachel; Cavelaars, Adriënne; de Groot, Lisette; van't Veer, Pieter; Gurinović, Mirjana

2014-03-01

The objective of this systematic review was to identify studies investigating iodine intake and biomarkers of iodine status, to assess the data of the selected studies, and to estimate dose-response relationships using meta-analysis. All randomized controlled trials, prospective cohort studies, nested case-control studies, and cross-sectional studies that supplied or measured dietary iodine and measured iodine biomarkers were included. The overall pooled regression coefficient (β) and the standard error of β were calculated by random-effects meta-analysis on a double-log scale, using the calculated intake-status regression coefficient (β) for each individual study. The results of pooled randomized controlled trials indicated that the doubling of dietary iodine intake increased urinary iodine concentrations by 14% in children and adolescents, by 57% in adults and the elderly, and by 81% in pregnant women. The dose-response relationship between iodine intake and biomarkers of iodine status indicated a 12% decrease in thyroid-stimulating hormone and a 31% decrease in thyroglobulin in pregnant women. The model of dose-response quantification used to describe the relationship between iodine intake and biomarkers of iodine status may be useful for providing complementary evidence to support recommendations for iodine intake in different population groups.

Carbon, cesium and iodine isotopes in Japanese cedar leaves from Iwaki, Fukushima.

Science.gov (United States)

Xu, Sheng; Cook, Gordon T; Cresswell, Alan J; Dunbar, Elaine; Freeman, Stewart P H T; Hou, Xiaolin; Kinch, Helen; Naysmith, Philip; Sanderson, David W C; Zhang, Luyuan

2016-01-01

Japanese cedar leaves from Iwaki, Fukushima were analyzed for carbon, cesium and iodine isotopic compositions before and after the 2011 nuclear accident. The Δ 14 C values reflect ambient atmospheric 14 C concentrations during the year the leaves were sampled/defoliated, and also previous year(s). The elevated 129 I and 134,137 Cs concentrations are attributed to direct exposure to the radioactive fallout for the pre-fallout-expended leaves and to internal translocation from older parts of the tree for post-fallout-expended leaves. 134 Cs/ 137 Cs and 129 I/ 137 Cs activity ratios suggest insignificant isotopic and elemental fractionation during translocation. However, fractionation between radioiodine and radiocesium is significant during transportation from the source.

Carbon, cesium and iodine isotopes in Japanese cedar leaves from Iwaki, Fukushima

International Nuclear Information System (INIS)

Sheng Xu; Cresswell, A.J.; Cook, G.T.; Dunbar, Elaine; Freeman, S.P.H.T.; Kinch, Helen; Naysmith, Philip; Sanderson, D.W.C.; Xiaolin Hou; Luyuan Zhang; Xi'an AMS Center, SKLLQG, CAS, Xi'an

2016-01-01

Japanese cedar leaves from Iwaki, Fukushima were analyzed for carbon, cesium and iodine isotopic compositions before and after the 2011 nuclear accident. The Δ 14 C values reflect ambient atmospheric 14 C concentrations during the year the leaves were sampled/defoliated, and also previous year(s). The elevated 129 I and 134,137 Cs concentrations are attributed to direct exposure to the radioactive fallout for the pre-fallout-expended leaves and to internal translocation from older parts of the tree for post-fallout-expended leaves. 134 Cs/ 137 Cs and 129 I/ 137 Cs activity ratios suggest insignificant isotopic and elemental fractionation during translocation. However, fractionation between radioiodine and radiocesium is significant during transportation from the source. (author)