Ecological considerations of natural and depleted uranium

International Nuclear Information System (INIS)

Hanson, W.C.

1980-01-01

Depleted 238 U is a major by-product of the nuclear fuel cycle for which increasing use is being made in counterweights, radiation shielding, and ordnance applications. This paper (1) summarizes the pertinent literature on natural and depleted uranium in the environment, (2) integrates results of a series of ecological studies conducted at Los Alamos Scientific Laboratory (LASL) in New Mexico where 70,000 kg of depleted and natural uranium has been expended to the environment over the past 34 years, and (3) synthesizes the information into an assessment of the ecological consequences of natural and depleted uranium released to the environment by various means. Results of studies of soil, plant, and animal communities exposed to this radiation and chemical environment over a third of a century provide a means of evaluating the behavior and effects of uranium in many contexts

The Chemistry and Toxicology of Depleted Uranium

OpenAIRE

Sidney A. Katz

2014-01-01

Natural uranium is comprised of three radioactive isotopes: 238U, 235U, and 234U. Depleted uranium (DU) is a byproduct of the processes for the enrichment of the naturally occurring 235U isotope. The world wide stock pile contains some 1½ million tons of depleted uranium. Some of it has been used to dilute weapons grade uranium (~90% 235U) down to reactor grade uranium (~5% 235U), and some of it has been used for heavy tank armor and for the fabrication of armor-piercing bullets and missiles....

Track Detection Technique Using CR-39 for Determining Depleted Uranium in Biological Specimens

International Nuclear Information System (INIS)

Murbat, S.M.

2013-01-01

Track detecting technique using CR-39 track detector has been implemented for determining depleted uranium concentration in biological specimens (tissues, bones, and blood) of patients infected with cancer diseases. Results were compared with specimens of patients infected with conventional diseases (noncancerous). Specimens were collected from middle and south of Iraq have been contaminated with depleted uranium in the Gulf war in 1991. Results show that this technique is efficient for determining depleted uranium concentration in biological specimens. It was found that all studies samples determine for patients infected with cancer diseases contain a high concentration of depleted uranium (more than the international standard) comparing with noncancerous diseases. Moreover, it was found that persons infected with Leukemia show more sensitive to uranium concentrations to induce the diseases (66-202 ppb), while (116- 1910 ppb) concentrations were needed for inducing cancer diseases in organs and tissues. Result confirmed the correlation between cancerous diseases and the munitions made of depleted uranium used in the Gulf war in 1991 leads to contaminate the Iraqi environment and causes a high risk against people in Iraq.

Challenges dealing with depleted uranium in Germany - Reuse or disposal

International Nuclear Information System (INIS)

Moeller, Kai D.

2007-01-01

During enrichment large amounts of depleted Uranium are produced. In Germany every year 2.800 tons of depleted uranium are generated. In Germany depleted uranium is not classified as radioactive waste but a resource for further enrichment. Therefore since 1996 depleted Uranium is sent to ROSATOM in Russia. However it still has to be dealt with the second generation of depleted Uranium. To evaluate the alternative actions in case a solution has to be found in Germany, several studies have been initiated by the Federal Ministry of the Environment. The work that has been carried out evaluated various possibilities to deal with depleted uranium. The international studies on this field and the situation in Germany have been analyzed. In case no further enrichment is planned the depleted uranium has to be stored. In the enrichment process UF 6 is generated. It is an international consensus that for storage it should be converted to U 3 O 8 . The necessary technique is well established. If the depleted Uranium would have to be characterized as radioactive waste, a final disposal would become necessary. For the planned Konrad repository - a repository for non heat generating radioactive waste - the amount of Uranium is limited by the licensing authority. The existing license would not allow the final disposal of large amounts of depleted Uranium in the Konrad repository. The potential effect on the safety case has not been roughly analyzed. As a result it may be necessary to think about alternatives. Several possibilities for the use of depleted uranium in the industry have been identified. Studies indicate that the properties of Uranium would make it useful in some industrial fields. Nevertheless many practical and legal questions are open. One further option may be the use as shielding e.g. in casks for transport or disposal. Possible techniques for using depleted Uranium as shielding are the use of the metallic Uranium as well as the inclusion in concrete. Another

Depleted uranium processing and fluorine extraction

International Nuclear Information System (INIS)

Laflin, S.T.

2010-01-01

Since the beginning of the nuclear era, there has never been a commercial solution for the large quantities of depleted uranium hexafluoride generated from uranium enrichment. In the United States alone, there is already in excess of 1.6 billion pounds (730 million kilograms) of DUF_6 currently stored. INIS is constructing a commercial uranium processing and fluorine extraction facility. The INIS facility will convert depleted uranium hexafluoride and use it as feed material for the patented Fluorine Extraction Process to produce high purity fluoride gases and anhydrous hydrofluoric acid. The project will provide an environmentally friendly and commercially viable solution for DUF_6 tails management. (author)

Long-term management and use of depleted uranium

International Nuclear Information System (INIS)

Max, A.

2001-01-01

The products resulting from the process of enrichment of natural uranium, or reprocessed uranium, are enriched uranium products as the light fraction and depleted uranium (uranium tails) as the heavy fraction. If the source material is natural uranium, the mass ratios of uranium products and uranium tails can be derived relatively easily from the required enrichment level of the uranium product (product assay (% of U-235)) and the selected depletion level of the uranium tails (tails assay (% of U-235)). The paper discusses among other aspects the dependence of the tails mass on the required enrichment level of the relevant uranium product, for various tails assays. (orig./CB) [de

Depleted uranium. A post-war disaster for environment and health

International Nuclear Information System (INIS)

Diehl, P.; Fahey, D.; Bertell, R.; Robicheau, D.; Bristow, R.; Arbuthnot, F.; Van der Keur, H.

1999-05-01

In the course of the preparations for the The Hague Appeal for Peace '99 conference in the Netherlands, Laka decided to make a brochure about the use of depleted uranium in conventional weaponry and its consequences. The idea was born because of the short time reserved during the session for the presentation of all details about depleted uranium (DU). Although the word 'depleted uranium' may suggest no harmful impact from radiation, this brochure will clarify the real radiotoxic (and chemotoxic) properties of DU. Laka asked several 'insiders' to take part in the completion of the brochure. Thanks to their efforts, we have been able to present well-documented articles for activists, scientists, scholars and students to share with them valuable information about the hazardous impact of DU contamination and its consequences on human health and the environment. Taking notice of the growing military use of DU, we must consider not only the increased threats of radioactive battlefields but also the whole dirty cycle in the uranium industry connected with the DU technology and its impact on health and the environment in the surroundings of test areas and in the uranium industry itself. The contents of all the contributions are under the responsibility of the authors.The titles of the contributions are (1) Depleted uranium. A by-product of the nuclear chain; (2) Depleted uranium weapons. Lessons from the 1991 Gulf War; (3) Gulf War veterans and depleted uranium; (4) The next testing site for depleted uranium weaponry; (5) Depleted uranium. The thoughts of the first British Gulf War veteran to be tested for, and found to be poisoned with depleted uranium; (6) The health of the Iraqi people; (7) Uranium pollution from the amsterdam 1992 plane crash; and (8) an overview od organizations involved in campaigns against depleted uranium. refs

Meta-analysis of depleted uranium levels in the Balkan region.

Science.gov (United States)

Besic, Larisa; Muhovic, Imer; Asic, Adna; Kurtovic-Kozaric, Amina

2017-06-01

In recent years, contradicting data has been published on the connection between the presence of depleted uranium and an increased cancer incidence among military personnel deployed in the Balkans during the 1992-1999 wars. This has led to numerous research articles investigating possible depleted uranium contamination of the afflicted regions of the Balkan Peninsula, namely Bosnia & Herzegovina, Serbia, Kosovo and Montenegro. The aim of this study was to collect data from previously published reports investigating the levels of depleted uranium in the Balkans and to present the data in the form of a meta-analysis. This would provide a clear image of the extent of depleted uranium contamination after the Balkan conflict. In addition, we tested the hypothesis that there is a correlation between the levels of depleted uranium and the assumed depleted uranium-related health effects. Our results suggest that the majority of the examined sites contain natural uranium, while the area of Kosovo appears to be most heavily afflicted by depleted uranium pollution, followed by Bosnia & Herzegovina. Furthermore, the results indicate that it is not possible to make a valid correlation between the health effects and depleted uranium-contaminated areas. We therefore suggest a structured collaborative plan of action where long-term monitoring of the residents of depleted uranium-afflicted areas would be performed. In conclusion, while the possibility of depleted uranium toxicity in post-conflict regions appears to exist, there currently exists no definitive proof of such effects, due to insufficient studies of potentially afflicted populations, in addition to the lack of a common epidemiological approach in the reviewed literature. Copyright © 2017 Elsevier Ltd. All rights reserved.

Uranium, depleted uranium, biological effects; Uranium, uranium appauvri, effets biologiques

Energy Technology Data Exchange (ETDEWEB)

NONE

2001-07-01

Physicists, chemists and biologists at the CEA are developing scientific programs on the properties and uses of ionizing radiation. Since the CEA was created in 1945, a great deal of research has been carried out on the properties of natural, enriched and depleted uranium in cooperation with university laboratories and CNRS. There is a great deal of available data about uranium; thousands of analyses have been published in international reviews over more than 40 years. This presentation on uranium is a very brief summary of all these studies. (author)

Research on using depleted uranium as nuclear fuel for HWR

International Nuclear Information System (INIS)

Zhang Jiahua; Chen Zhicheng; Bao Borong

1999-01-01

The purpose of our work is to find a way for application of depleted uranium in CANDU reactor by using MOX nuclear fuel of depleted U and Pu instead of natural uranium. From preliminary evaluation and calculation, it was shown that MOX nuclear fuel consisting of depleted uranium enrichment tailings (0.25% 235 U) and plutonium (their ratio 99.5%:0.5%) could replace natural uranium in CANDU reactor to sustain chain reaction. The prospects of application of depleted uranium in nuclear energy field are also discussed

Depleted uranium hexafluoride: Waste or resource?

International Nuclear Information System (INIS)

Schwertz, N.; Zoller, J.; Rosen, R.; Patton, S.; Bradley, C.; Murray, A.

1995-07-01

The US Department of Energy is evaluating technologies for the storage, disposal, or re-use of depleted uranium hexafluoride (UF 6 ). This paper discusses the following options, and provides a technology assessment for each one: (1) conversion to UO 2 for use as mixed oxide duel, (2) conversion to UO 2 to make DUCRETE for a multi-purpose storage container, (3) conversion to depleted uranium metal for use as shielding, (4) conversion to uranium carbide for use as high-temperature gas-cooled reactor (HTGR) fuel. In addition, conversion to U 3 O 8 as an option for long-term storage is discussed

Environmental fate of depleted uranium at three sites contaminated during the balkan conflict

International Nuclear Information System (INIS)

Radenkovic, M.; Joksic, J.; Todorovic, D.; Kovacevic, M.

2006-01-01

A study on depleted uranium fate in the sites contaminated during the 1999 war conflict in Serbia was conducted in phases until the clean up activities were completed. The ammunition remains found at the locations in the surface soil were collected in the first phase during the radiation survey of the affected areas. The most of depleted uranium penetrators left buried deep into the ground exposed to the weathering and corrosion processes. The contamination level in the air, water, soil and bio -indicators was controlled all the time by routine gamma and alpha spectrometry measurements. Depleted uranium migration was studied through the soil profile surrounding the penetrator during the 2001 at the Bratoselce location showing the contamination level fall to the 1% of its value at approximately 15 cm distance to the source. The samples taken from the soil layers at different distances in the profile are subjected to a modified Tessiers five-step sequential extraction procedure. The uranium and heavy metals contents were determined in the obtained fractions. Results have specified carbonates and iron hydrous-oxides as the most probable substrates for uranium physical/chemical associations formed in the soil for the time elapsed. A very strong dependence of substrate onto contamination level was found. The correlation of uranium and other heavy metals was obtained. The 234 U/ 238 U and 235 U/ 238 U ratios are determined in extracts by alpha spectrometry after appropriate radiochemical separation procedure and thin alpha sources electroplating. The analysis has shown the share of depleted in total uranium content in exchangeable, carbonate, hydrous or crystalline iron/manganese, organic and residue phases indicating the bioavailability of depleted uranium present in the soil. The results are discussed related to detailed geochemical analysis of the particular soil type common for this region. Depleted uranium content in soil samples taken at the locations after the

Depleted uranium hexafluoride: Waste or resource?

Energy Technology Data Exchange (ETDEWEB)

Schwertz, N.; Zoller, J.; Rosen, R.; Patton, S. [Lawrence Livermore National Lab., CA (United States); Bradley, C. [USDOE Office of Nuclear Energy, Science, Technology, Washington, DC (United States); Murray, A. [SAIC (United States)

1995-07-01

the US Department of Energy is evaluating technologies for the storage, disposal, or re-use of depleted uranium hexafluoride (UF{sub 6}). This paper discusses the following options, and provides a technology assessment for each one: (1) conversion to UO{sub 2} for use as mixed oxide duel, (2) conversion to UO{sub 2} to make DUCRETE for a multi-purpose storage container, (3) conversion to depleted uranium metal for use as shielding, (4) conversion to uranium carbide for use as high-temperature gas-cooled reactor (HTGR) fuel. In addition, conversion to U{sub 3}O{sub 8} as an option for long-term storage is discussed.

Radioactive reconnaissance in area of utilization ammunition of depleted uranium

International Nuclear Information System (INIS)

Fortuna, D.; Dimitrijevic, D.

2000-01-01

In this paper are presented methods of radioactive reconnaissance and taking of samples in area of utilization ammunition of depleted uranium during the armed aggression of NATO to Yugoslavia (author)

Bullet scintigraphy: can gamma camera be used for depleted uranium accident measurements?

International Nuclear Information System (INIS)

Spaic, R.; Markovic, S.; Pavlovic, S.; Radic, Z.; Pavlovic, R.; Ajdinovic, B.; Baskot, B.; Djurovic, B.

2002-01-01

The aim of this study was to see could gamma cameras be used for measurement of internal contamination with depleted uranium. Radioactive waste depleted uranium, which is by-product from the production of enriched fuel for nuclear rectors and weapons now, is used for manufacture bullets, which are used in Iraq, Republic of Srpska and Yugoslavia. In this paper is measured minimum detectable activity (MDA) of gamma cameras for depleted uranium, iodine and technetium. For detection of the depleted uranium are used low energy X-rays, energy of 100 keV with 20% windows width. About 40% of gamma emissions of the depleted uranium are in these limits. Measured MDA activities 50-100 Bq for depleted uranium, iodine and technetium are about then times more then same for WBC (5 Bq). Gamma cameras can be used for relatively measurement of depleted uranium activity, what can be used for absorbed dose estimation. Detection of low level internal contamination with depleted uranium can be done with gamma cameras. (authors)

Early results of studies on the levels of depleted uranium excreted by Balkan residents

International Nuclear Information System (INIS)

Priest, N.D.; Thirlwell, M.

2002-01-01

Urine samples collected from residents of Bosnia and Herzegovina and Kosovo were analysed to determine their natural and depleted uranium content using MC-ICP-MS. All may have been exposed to depleted uranium released as a consequence of the deployment of armour-piercing rounds by the US Air Force. A 236 U tracer was employed to determine chemical recovery. Early results suggest that the levels of natural and depleted uranium excretion by the subjects, which ranged in age from 1 to 71 years, ranged from 2.8 - 58.2 ng d -1 and 1.3 - 46.3 ng d -1 , respectively. The results suggest accumulated body burdens of depleted uranium ranging from close to zero to 46 μg. All the body burdens predicted are lower than published values for the uranium content of the body (90μg) and health effects are not predicted. Further studies are underway to check the provenance of the results. (author)

Depleted uranium management alternatives

Energy Technology Data Exchange (ETDEWEB)

Hertzler, T.J.; Nishimoto, D.D.

1994-08-01

This report evaluates two management alternatives for Department of Energy depleted uranium: continued storage as uranium hexafluoride, and conversion to uranium metal and fabrication to shielding for spent nuclear fuel containers. The results will be used to compare the costs with other alternatives, such as disposal. Cost estimates for the continued storage alternative are based on a life-cycle of 27 years through the year 2020. Cost estimates for the recycle alternative are based on existing conversion process costs and Capital costs for fabricating the containers. Additionally, the recycle alternative accounts for costs associated with intermediate product resale and secondary waste disposal for materials generated during the conversion process.

Depleted uranium management alternatives

International Nuclear Information System (INIS)

Hertzler, T.J.; Nishimoto, D.D.

1994-08-01

This report evaluates two management alternatives for Department of Energy depleted uranium: continued storage as uranium hexafluoride, and conversion to uranium metal and fabrication to shielding for spent nuclear fuel containers. The results will be used to compare the costs with other alternatives, such as disposal. Cost estimates for the continued storage alternative are based on a life-cycle of 27 years through the year 2020. Cost estimates for the recycle alternative are based on existing conversion process costs and Capital costs for fabricating the containers. Additionally, the recycle alternative accounts for costs associated with intermediate product resale and secondary waste disposal for materials generated during the conversion process

Depleted uranium and the Gulf War syndrome

International Nuclear Information System (INIS)

1999-01-01

Some military personnel involved in the 1991Gulf War have complained of continuing stress-like symptoms for which no obvious cause has been found. These symptoms have at times been attributed to the use of depleted uranium (DU) in shell casings which are believed to have caused toxic effects. Depleted uranium is natural uranium which is depleted in the rarer U-235 isotope. It is a heavy metal and in common with other heavy metals is chemically toxic. It is also slightly radioactive and could give rise to a radiological hazard if dispersed in finely divided form so that it was inhaled. In response to concerns, the possible effects of DU have been extensively studied along with other possible contributors to G ulf War sickness . This article looks at the results of some of the research that has been done on DU. (author)

The manufacturing of depleted uranium biological shield components

International Nuclear Information System (INIS)

Metelkin, J.A.

1998-01-01

The unique combination of the physical and mechanical properties of uranium made it possible to manufacture biological shield components of transport package container (TPC) for transportation nuclear power plant irradiated fuel and radionuclides of radiation diagnostic instruments. Protective properties are substantially dependent on the nature radionuclide composition of uranium, that why I recommended depleted uranium after radiation chemical processing. Depleted uranium biological shield (DUBS) has improved specific mass-size characteristics compared to a shield made of lead, steel or tungsten. Technological achievements in uranium casting and machining made it possible to manufacture DUBS components of TPC up to 3 tons of mass and up to 2 metres of the maximum size. (authors)

Radioactivity of drinking waters from regions exposed to depleted uranium ammunition bombing in 2003 end 2004

International Nuclear Information System (INIS)

Tanaskovic, I.; Pantelic, G.; Vuletic, V.; Eremic Savkovic, M.; Javorina, L.J.

2006-01-01

Due to the military application of the depleted uranium in our country, the problem of its radioactivity and hemo toxicity is actualized. The locations verified to be contaminated by depleted uranium ammunition were at the South part of Serbia (Pljackovica, Bratoselce, Borovac and Reljan). The soluble forms of uranium could translocated and dispersed from soils and sediments into surface waters and groundwater. The environmental presence of depleted uranium is considered as potential threat to human health. The study presents the results of radiological safety analysis of drinking water in 2003 and 2004. All samples were analyzed by gamma spectrometry and measurements of alpha and beta activity. (authors)

The ultimate disposition of depleted uranium

Energy Technology Data Exchange (ETDEWEB)

1990-12-01

Significant amounts of the depleted uranium (DU) created by past uranium enrichment activities have been sold, disposed of commercially, or utilized by defense programs. In recent years, however, the demand for DU has become quite small compared to quantities available, and within the US Department of Energy (DOE) there is concern for any risks and/or cost liabilities that might be associated with the ever-growing inventory of this material. As a result, Martin Marietta Energy Systems, Inc. (Energy Systems), was asked to review options and to develop a comprehensive plan for inventory management and the ultimate disposition of DU accumulated at the gaseous diffusion plants (GDPs). An Energy Systems task team, under the chairmanship of T. R. Lemons, was formed in late 1989 to provide advice and guidance for this task. This report reviews options and recommends actions and objectives in the management of working inventories of partially depleted feed (PDF) materials and for the ultimate disposition of fully depleted uranium (FDU). Actions that should be considered are as follows. (1) Inspect UF{sub 6} cylinders on a semiannual basis. (2) Upgrade cylinder maintenance and storage yards. (3) Convert FDU to U{sub 3}O{sub 8} for long-term storage or disposal. This will include provisions for partial recovery of costs to offset those associated with DU inventory management and the ultimate disposal of FDU. Another recommendation is to drop the term tails'' in favor of depleted uranium'' or DU'' because the tails'' label implies that it is waste.'' 13 refs.

Electrochemical corrosion behavior of MSIP Ni coating on depleted uranium surface

International Nuclear Information System (INIS)

Chen Lin; Li Kexue; Wang Qingfu; Wang Xiaohong; Guan Weijun

2014-01-01

The Ni film was prepared by magnetron sputtering ion plating to improve the corrosion resistance of depleted uranium. The corrosion resistance of the Ni film was examined by electrochemical corrosion station. The results show that the Ni film corrosion potential is -100.8 mV, whereas it is -641.2 mV for depleted uranium in 50 μg/g KCl solution. The Ni film is a barrier to protect the depleted uranium substrate avoiding the corrosive media attack. The Ni film polarization resistance and impedance are much higher, while the corrosion current density is much lower contrast with depleted uranium. None crack or flake is found through 70 h corrosion. The corrosion resistance and corrosion current keep stable. It is indicated that the corrosion resistance of depleted uranium is effectively improved after deposited Ni film by magnetron sputtering ion plating. (authors)

On problems related to the deployment of depleted uranium weapons in the Balkans

International Nuclear Information System (INIS)

Mietelski, J. W.; Waligorski, M.P.R.; Zunic, Z.S.

2002-01-01

The likely long-term environmental and health effects of the deployment of weapons containing depleted uranium (DU) in the Balkans are discussed. To determine whether depleted uranium or spent reactor fuel was used in the weapons, knowledge is required of the 235 U to 238 U activity (or concentration) ratio in the measured samples. To this end, and to distinguish between uranium originating from natural and man-made sources, we discuss some of the methodology and metrology issues involved in performing alpha- and gamma- spectrometry of uranium in environmental and human samples. We present results of nuclear spectrometry performed on DU core deposits from the aluminium jacket of a PGU-14 bullet found in South Serbia. We draw attention to aspects involving ionising radiation, which are likely to be of importance when formulating a prognosis of the possible environmental and health impact of the deployment of DU weapons, indicating the importance of the inhalation pathway in children. (author)

Retrieval of buried depleted uranium from the T-1 trench

International Nuclear Information System (INIS)

Burmeister, M.; Castaneda, N.; Hull, C.; Barbour, D.; Quapp, W.J.

1998-01-01

The Trench 1 remediation project will be conducted this year to retrieve depleted uranium and other associated materials from a trench at Rocky Flats Environmental Technology Site. The excavated materials will be segregated and stabilized for shipment. The depleted uranium will be treated at an offsite facility which utilizes a novel approach for waste minimization and disposal through utilization of a combination of uranium recycling and volume efficient uranium stabilization

Yield, utilization, storage and ultimate storage of depleted uranium

International Nuclear Information System (INIS)

Aumueller, L.; Hermann, J.

1977-11-01

More than 80% of the uranium leaving uranium enrichment plants is depleted to a residual content of about 0,25% U 235. Due to the present ineconomical further depletion to the technically possible residual content of 0,1% U 235, the so-called 'tails' are first of all stored. The quantity of stored depleted uranium in the FRG should be about 100.000 t by the year 2000. It represents a strategic reserve for future energy supply regardless of profitableness. The study analysis the conceivable possible uses for the tails quantity considered. These are, besides further depletion whose profitableness is considered, also the use as breeder material in breeder reactors and the use in the non-nuclear field. The main part of the study deals with the various storage possibilities of the depleted uranium in oxidic or fluoride form. A comparison of costs of alternative storage concepts showed a clear advantage for the storage of UF 6 in 48 inch containers already in use. The conceivable accidents in storing are analyzed and measures to reduce the consequences are discussed. Finally, the problems of ultimate storage for the remaining waste after further depletion or use are investigated and the costs arising here are also estimated. (RB) [de

Effect of intratracheally instilled depleted uranium on immunological function of rats

International Nuclear Information System (INIS)

You Hanhu; Yang Zhihua; Cao Zhenshan; Zhu Maoxiang; Liu Xingrong

2004-01-01

Objective: To study immunological effects of depleted uranium in rats. Methods: Wistar rats were exposed to depleted uranium by single intratracheal instillation. Body weight and peripheral blood cells were measured weekly and immunological functions were evaluated by weight coefficient of immune organs, plague forming cells of splenocytes, total and subpopulation counts of lymphocytes in thymus. Results: Early after administration, body weight decreased and red blood cells as well as platelets reduced while white blood cells increased, which returned to normal within 1 or 2 months. Immunological functions of splenocytes and thymocytes were affected dose-dependently by depleted uranium. Conclusion: Depleted uranium induces immunological dysfunction in rats. (authors)

Depleted uranium - influence on the health and environment; Ochudobneny uran - vplyva na zdravie a zivotne prostredie

Energy Technology Data Exchange (ETDEWEB)

Rosskopfova, O [Katedra jadrovej chemie, Prirodovedecka fakulta, Univerzita Komenskeho, Bratislava (Slovakia)

2002-07-01

The uranium as radioactive element occurs in low concentrations in all components of environment. In the sample of natural uranium the isotope U-235 has the highest share (99.27 weight per cent). Chemical toxicity of uranium is comparable with toxicity of the elements like As and Pb. Depleted uranium is adjoining product in the production of enriched uranium, which is required in the production of the nuclear fuel and in the production of material used in nuclear arms. It mainly includes isotope U-238, and the content of isotopes U-235 and U-234 is sharply lowered. According to NRC depleted uranium is defined like uranium, in which percentile share of isotope U-235 is less than 0.711 weight percent. The activity of depleted uranium from viewpoint of external irradiation does not represent higher risk. Much higher risk for man represent the neurotoxic effects of uranium, which can get into human body by inhaling of dispersed particles, of contaminated dust and aerosols from atmosphere or by consumption of contaminated foodstuffs and water. Basic dangerous of irradiation by depleted uranium are mainly aerosols, which increase the probability of occurrence of lung cancer. The next dangerous is the damage of another organs like kidneys, liver and bones, where these aerosols are transported by blood like oxides from the lungs. In the environmental parts because of presence of natural uranium the depleted uranium is difficultly identifiably by standard detective methods. Thus it is necessary to use suitable radiochemical separative methods in combination with suitable detective method. (author)

Depleted uranium plasma reduction system study

International Nuclear Information System (INIS)

Rekemeyer, P.; Feizollahi, F.; Quapp, W.J.; Brown, B.W.

1994-12-01

A system life-cycle cost study was conducted of a preliminary design concept for a plasma reduction process for converting depleted uranium to uranium metal and anhydrous HF. The plasma-based process is expected to offer significant economic and environmental advantages over present technology. Depleted Uranium is currently stored in the form of solid UF 6 , of which approximately 575,000 metric tons is stored at three locations in the U.S. The proposed system is preconceptual in nature, but includes all necessary processing equipment and facilities to perform the process. The study has identified total processing cost of approximately $3.00/kg of UF 6 processed. Based on the results of this study, the development of a laboratory-scale system (1 kg/h throughput of UF6) is warranted. Further scaling of the process to pilot scale will be determined after laboratory testing is complete

Partitioning ratio of depleted uranium during a melt decontamination by arc melting

International Nuclear Information System (INIS)

Min, Byeong Yeon; Choi, Wang Kyu; Oh, Won Zin; Jung, Chong Hun

2008-01-01

In a study of the optimum operational condition for a melting decontamination, the effects of the basicity, slag type and slag composition on the distribution of depleted uranium were investigated for radioactively contaminated metallic wastes of iron-based metals such as stainless steel (SUS 304L) in a direct current graphite arc furnace. Most of the depleted uranium was easily moved into the slag from the radioactive metal waste. The partitioning ratio of the depleted uranium was influenced by the amount of added slag former and the slag basicity. The composition of the slag former used to capture contaminants such as depleted uranium during the melt decontamination process generally consists of silica (SiO 2 ), calcium oxide (CaO) and aluminum oxide (Al 2 O 3 ). Furthermore, calcium fluoride (CaF 2 ), magnesium oxide (MgO), and ferric oxide (Fe 2 O 3 ) were added to increase the slag fluidity and oxidative potential. The partitioning ratio of the depleted uranium was increased as the amount of slag former was increased. Up to 97% of the depleted uranium was captured between the ingot phase and the slag phase. The partitioning ratio of the uranium was considerably dependent on the basicity and composition of the slag. The optimum condition for the removal of the depleted uranium was a basicity level of about 1.5. The partitioning ratio of uranium was high, exceeding 5.5x10 3 . The slag formers containing calcium fluoride (CaF 2 ) and a high amount of silica proved to be more effective for a melt decontamination of stainless steel wastes contaminated with depleted uranium

Concentration and characteristics of depleted uranium in biological and water samples collected in Bosnia and Herzegovina

International Nuclear Information System (INIS)

Jia Guogang; Belli, Maria; Sansone, Umberto; Rosamilia, Silvia; Gaudino, Stefania

2006-01-01

During Balkan conflicts in 1994-1995, depleted uranium (DU) ordnance was employed and was left in the battlefield. Health concern is related to the risk arising from contamination of the environment with DU penetrators and dust. In order to evaluate the impact of DU on the environment and population in Bosnia and Herzegovina, radiological survey of DU in biological and water samples were carried out over the period 12-24 October 2002. The uranium isotopic concentrations in biological samples collected in Bosnia and Herzegovina, mainly lichens, mosses and barks, were found to be in the range of 0.27-35.7 Bq kg -1 for 238 U, 0.24-16.8 Bq kg -1 for 234 U, and 0.02-1.11 Bq kg -1 for 235 U, showing uranium levels to be higher than in the samples collected at the control site. Moreover, the 236 U in some of the samples was detectable. The isotopic ratios of 234 U/ 238 U showed DU to be detectable in many biological samples at most sites examined, but in very low levels. The presence of DU in the biological samples was as a result of DU contamination in air. The uranium concentrations in water samples collected in Bosnia and Herzegovina were found to be in the range of 0.27-16.2 mBq l -1 for 238 U, 0.41-15.6 mBq l -1 for 234 U and 0.012-0.695 mBq l -1 for 235 U, and two water samples were observed to be DU positive; these values are much lower than those in mineral water found in central Italy and below the WHO guideline for public drinking water. From radiotoxicological point of view, at this moment there is no significant radiological risk related to these investigated sites in terms of possible DU contamination of water and/or plants

Uranium and the use of depleted uranium in weaponry

International Nuclear Information System (INIS)

Roussel, R.

2000-01-01

In this brief report the author shows that the use of shells involving a load of depleted uranium might lead to lasting hazards to civil population and environment. These hazards come from the part of the shell that has been dispersed as contaminating radioactive dusts. The author describes some features of radioactivity and highlights the role of Uranium-238 as a provider of energy to the planet. (A.C.)

Results of the analysis of the intercomparison samples of the depleted uranium dioxide SR-20

International Nuclear Information System (INIS)

Aigner, H.; Deron, S.; Kuhn, E.; Ronesch, K.; Zoigner, A.

Samples of a homogeneous powder of depleted uranium dioxide, SR-20, were distributed to 32 laboratories in January 1980 for intercomparison of the precisions and accuracies of wet chemical assay. 11 laboratories reported their results (ANNEX 1). 5 laboratories applied titration procedures, 4 of them applied methods derived from the Davies and Gray procedure (1), 2 laboratories used controlled potential coulometry, 2 laboratories used precipitation procedures, 1 laboratory used fluorimetry and 1 laboratory used activation analysis. An analysis of variance yields for each laboratory the estimates of the measurement errors, the dissolution or treatment errors and the random calibration errors. The measurement errors vary between 0.01% and 1.7% relative. The differences to the reference value vary between -9.1% and +0.92% uranium, but 9 laboratories agree within +-1%U with the reference value. The mean bias of these 9 laboratories is equal to +0.04%U. The standard deviation of the biases of these 9 laboratories is equal to 0.36%.U

Results of the analysis of the intercomparison samples of the depleted uranium dioxide SR-10

International Nuclear Information System (INIS)

Aigner, H.; Deron, S.; Kuhn, E.; Zoigner, A.

1981-01-01

Samples of a homogeneous powder of depleted uranium dioxide, SR-10, were distributed to 27 laboratories in February 1979 for intercomparison of the precisions and accuracies of wet chemical assay. 7 laboratories reported their results. 6 laboratories applied titration procedures, 4 of them applied methods derived from the Davies and Gray procedure (1), and one laboratory used controlled potential coulometry. An analysis of variance yields for each laboratory the estimates of the measurement errors, the dissolution or treatment errors and the random calibration errors. The measurement errors vary between 0.01% and 0.10% relative. The differences to the reference value vary between -0.48% and +0.87% uranium, but 5 laboratories agree within +-0.25% U with the reference value. The biases of 5 laboratories are greater than expected from their random errors. The mean bias of the 7 laboratories is equal to +0.03% U. The standard deviation of the laboratory biases is equal to 0.43% U. (author)

The ultimate disposition of depleted uranium

Energy Technology Data Exchange (ETDEWEB)

Lemons, T.R. [Uranium Enrichment Organization, Oak Ridge, TN (United States)

1991-12-31

Depleted uranium (DU) is produced as a by-product of the uranium enrichment process. Over 340,000 MTU of DU in the form of UF{sub 6} have been accumulated at the US government gaseous diffusion plants and the stockpile continues to grow. An overview of issues and objectives associated with the inventory management and the ultimate disposition of this material is presented.

Gamma spectrometric determination of depleted Uranium in Yugoslavia

International Nuclear Information System (INIS)

Pantelic, G.; Eremic Savkovic, M.; Javorina, L.; Tanaskovic, I.; Vuletic, V.; Milacic, S.

2002-01-01

The radiation protection is very important interdisciplinary research field due to the presence of the radiation in daily life. The systematic examination of radioactive contamination of various environmental samples was established forty years ago in the Institute of Occupational and Radiological Health Dr Dragomir Karajovic for the sake of preventive protection of population and environment from the harmful effect of ionizing radiation. The global sources of radionuclide contamination in our country are the fallout due to previous nuclear testing and the deposition of radionuclides from the region of Chernobyl accident. The contents of radionuclides were determined in aerosol, soil, fallout (wet and dry deposition), rivers, lakes, drinking water, human and animal food. The samples were collected in several locations of the Republic of Serbia and in regular time intervals, according to methods determined by the regulation. The regulations and the monitoring programs were updated after the Chernobyl accident. In the recent time, after the NATO aggression, we analyzed depleted uranium content in the environmental samples. We used high-resolution gamma spectrometry measurements, because of their simplicity and accuracy. Aims of the control were to asses the increase of radioactivity above the natural levels in the immediate and near vicinity of the bomb craters, to asses the corresponding effect of changed natural radioactivity on the health of the population living in these places and finding unexploded depleted uranium bullets

Concentration and characteristics of depleted uranium in water, air and biological samples collected in Serbia and Montenegro

International Nuclear Information System (INIS)

Jia Guogang; Belli, Maria; Sansone, Umberto; Rosamilia, Silvia; Gaudino, Stefania

2005-01-01

During the Balkan conflicts, in 1995 and 1999, depleted uranium (DU) rounds were employed and were left in the battlefield. Health concern is related to the risk arising from contamination of the environment with DU penetrators and dust. In order to evaluate the impact of DU on the environment and population in Serbia and Montenegro, radiological surveys of DU in water, air and biological samples were carried out over the period 27 October-5 November 2001. The uranium isotopic concentrations in biological samples collected in Serbia and Montenegro, mainly lichens and barks, were found to be in the range of 0.67-704 Bq kg -1 for 238 U, 0.48-93.9 Bq kg -1 for 234 U and 0.02-12.2 Bq kg -1 for 235 U, showing uranium levels to be higher than in the samples collected at the control sites. Moreover, 236 U was detectable in some of the samples. The isotopic ratios of 234 U/ 238 U showed DU to be detectable in many biological samples at all examined sites, especially in Montenegro, indicating widespread ground-surface DU contamination, albeit at very low level. The uranium isotopic concentrations in air obtained from the air filter samples collected in Serbia and Montenegro were found to be in the range of 1.99-42.1 μBq m -3 for 238 U, 0.96-38.0 μBq m -3 for 234 U, and 0.05-1.83 μBq m -3 for 235 U, being in the typical range of natural uranium values. Thus said, most of the air samples are DU positive, this fact agreeing well with the widespread DU contamination detected in the biological samples. The uranium concentrations in water samples collected in Serbia and Montenegro were found to be in the range of 0.40-21.9 mBq l -1 for 238 U, 0.27-28.1 mBq l -1 for 234 U, and 0.01-0.88 mBq l -1 for 235 U, these values being much lower than those in mineral water found in central Italy and below the WHO guideline for drinking water. From a radiotoxicological point of view, at this moment there is no significant radiological risk related to these investigated sites in terms of

Concentration and characteristics of depleted uranium in water, air and biological samples collected in Serbia and Montenegro.

Science.gov (United States)

Jia, Guogang; Belli, Maria; Sansone, Umberto; Rosamilia, Silvia; Gaudino, Stefania

2005-09-01

During the Balkan conflicts, in 1995 and 1999, depleted uranium (DU) rounds were employed and were left in the battlefield. Health concern is related to the risk arising from contamination of the environment with DU penetrators and dust. In order to evaluate the impact of DU on the environment and population in Serbia and Montenegro, radiological surveys of DU in water, air and biological samples were carried out over the period 27 October-5 November 2001. The uranium isotopic concentrations in biological samples collected in Serbia and Montenegro, mainly lichens and barks, were found to be in the range of 0.67-704 Bqkg(-1) for (238)U, 0.48-93.9 Bqkg(-1) for (234)U and 0.02-12.2 Bqkg(-1) for (235)U, showing uranium levels to be higher than in the samples collected at the control sites. Moreover, (236)U was detectable in some of the samples. The isotopic ratios of (234)U/(238)U showed DU to be detectable in many biological samples at all examined sites, especially in Montenegro, indicating widespread ground-surface DU contamination, albeit at very low level. The uranium isotopic concentrations in air obtained from the air filter samples collected in Serbia and Montenegro were found to be in the range of 1.99-42.1 microBqm(-3) for (238)U, 0.96-38.0 microBqm(-3) for (234)U, and 0.05-1.83 microBqm(-3) for (235)U, being in the typical range of natural uranium values. Thus said, most of the air samples are DU positive, this fact agreeing well with the widespread DU contamination detected in the biological samples. The uranium concentrations in water samples collected in Serbia and Montenegro were found to be in the range of 0.40-21.9 mBql(-1) for (238)U, 0.27-28.1 mBql(-1) for (234)U, and 0.01-0.88 mBql(-1) for (235)U, these values being much lower than those in mineral water found in central Italy and below the WHO guideline for drinking water. From a radiotoxicological point of view, at this moment there is no significant radiological risk related to these investigated

Metallographic Characterization of Wrought Depleted Uranium

Energy Technology Data Exchange (ETDEWEB)

Forsyth, Robert Thomas [Los Alamos National Lab. (LANL), Los Alamos, NM (United States); Hill, Mary Ann [Los Alamos National Lab. (LANL), Los Alamos, NM (United States)

2018-02-14

Metallographic characterization was performed on wrought depleted uranium (DU) samples taken from the longitudinal and transverse orientations from specific locations on two specimens. Characterization of the samples included general microstructure, inclusion analysis, grain size analysis, and microhardness testing. Comparisons of the characterization results were made to determine any differences based on specimen, sample orientation, or sample location. In addition, the characterization results for the wrought DU samples were also compared with data obtained from the metallographic characterization of cast DU samples previously characterized. No differences were observed in microstructure, inclusion size, morphology, and distribution, or grain size in regard to specimen, location, or orientation for the wrought depleted uranium samples. However, a small difference was observed in average hardness with regard to orientation at the same locations within the same specimen. The longitudinal samples were slightly harder than the transverse samples from the same location of the same specimen. This was true for both wrought DU specimens. Comparing the wrought DU sample data with the previously characterized cast DU sample data, distinct differences in microstructure, inclusion size, morphology and distribution, grain size, and microhardness were observed. As expected, the microstructure of the wrought DU samples consisted of small recrystallized grains which were uniform, randomly oriented, and equiaxed with minimal twinning observed in only a few grains. In contrast, the cast DU microstructure consisted of large irregularly shaped grains with extensive twinning observed in most grains. Inclusions in the wrought DU samples were elongated, broken and cracked and light and dark phases were observed in some inclusions. The mean inclusion area percentage for the wrought DU samples ranged from 0.08% to 0.34% and the average density from all wrought DU samples was 1.62E+04/cm

Examination of the health status of populations from depleted-uranium-contaminated regions

International Nuclear Information System (INIS)

Milacic, Snezana; Petrovic, Dragana; Jovicic, Dubravka; Kovacevic, Radomir; Simic, Jadranko

2004-01-01

During the NATO air strikes on the Federal Republic of Yugoslavia (Serbia and Montenegro) in 1999, depleted-uranium ammunition was used on 112 locations, mainly Kosovo, in the south of Serbia, and one location in Montenegro. Blood samples of residents from depleted-uranium-contaminated areas were gathered and blood cell and chromosomal aberrations were analyzed. During the last 3 years blood samples from 21 residents of Kosovo (Strpce), from 29 residents from the south of Serbia (the Vranje and Bujanovac regions), and from 19 technical television workers from the site of Pljackovica, in the vicinity of Vranje, were collected. Blood samples from 33 residents of central Serbia and 46 occupational workers exposed to X-rays were used as controls. All subjects studied were without any clinical symptoms of disease. The examinations included general clinical assessment; urine samples for α-and γ-spectrometry analysis; complete blood counts; ratio-percentages of blood cells in stained (Giemsa) capillary smears, individual leukocyte line elements; morphological changes observed under a microscope; the presence of immature forms or blasts; and leukocyte enzyme activity [alkaline phosphatase leukocyte (APL)]. Chromosomal aberrations were evaluated in 200 peripheral blood lymphocytes in mitosis. An increased incidence of rogue cells and chromosomal aberrations was found in the blood of the residents of Vranje and Bujanovac, but this was below the incidence of chromosomal aberrations in individuals occupationally exposed to ionizing irradiation. Blast cells were not found. Blood counts were decreased in only a few samples, while morphological changes of both nuclei and cytoplasm were marked in individuals in south and central Serbia. Enzymatic activity (as measured by the APL score) was decreased in samples with chromosomal aberrations and cyto-morphological changes in subjects from the south of Serbia. The contamination level measured by this examination was low. Because of

Toxicity of Depleted Uranium Dust Particles: Results of a New Model

International Nuclear Information System (INIS)

Zucchetti, M.

2013-01-01

Depleted uranium (DU) is mostly composed of U-238, a naturally radioactive isotope. Concerning chemical toxicity, uranium, being a heavy metal, is known to have toxic effects on specific organs in the body, the kidneys in particular. Its effects are similar to those of other heavy metals, such as lead and cadmium. Scientific evidence resulting both from in vitro and in vivo analyses shows that current models of the mechanisms of toxicity of uranium dust are not fully satisfactory. They should be refined in order to obtain more effective responses and predictions regarding health effects. In particular, radiotoxicity potential of Depleted Uranium dust originated by military use of this material for ammunition must be re-evaluated taking into account the bystander effect, the dose enhancing effect and other minor phenomena. Uranium dust has both chemical and radiological toxicity: the synergistic aspect of the two effects has to be accounted for, in order to arrive to a complete description of the phenomenon. The combination of the two different toxicities (chemical and radiological) of depleted uranium is attempted here for the first time, approaching the long-term effects of Depleted Uranium, and in particular the carcinogenetic effects. A case study (Balkan war, 1999) is discussed. (Author)

Health and environmental problems of using antiarmour munitions containing depleted uranium core

International Nuclear Information System (INIS)

Matousek, J.

2006-01-01

In the 1970s, core of depleted uranium commenced to be introduced into the breakthrough antitank munitions of various calibers and types in order to considerably enhance their effectiveness due to extremely high density in comparison with steel. The health and environmental threats of using this munitions and other weaponry where depleted uranium has been utilised as counterbalance stem from the pyrophoric character of uranium, burnt due to material deformation and friction when penetrating armour targets creating thus highly respirable aerosol of uranium oxides that are deposited in alveoli after being inhaled or in other tissues after being ingested. Composition and main properties of depleted uranium are presented. Chronic effects of deposited particles of uranium oxides are due to internal irradiation of sensitive organs at proceeding radioactive decay accompanied with alpha irradiation. Long-term internal irradiation by radionuclides producing alpha-rays leads to proved risk of increased incidence of carcinoma and leukaemia not to speak on chronic chemical toxicity of uranium, independent of its isotopic composition. Environmental impact of extensive use of munitions with depleted uranium in the recent armed conflicts is assessed. (authors)

Isotopic investigation of the colloidal mobility of depleted uranium in a podsolic soil

International Nuclear Information System (INIS)

Harguindeguy, S.; Crancon, P.; Pointurier, F.; Potin-Gautier, M.; Lespes, G.

2014-01-01

The mobility and colloidal migration of uranium were investigated in a soil where limited amounts of anthropogenic uranium (depleted in the "2"3"5U isotope) were deposited, adding to the naturally occurring uranium. The colloidal fraction was assumed to correspond to the operational fraction between 10 kDa and 1.2 μm after (ultra)filtration. Experimental leaching tests indicate that approximately 8-15% of uranium is desorbed from the soil. Significant enrichment of the leachate in the depleted uranium (DU) content indicates that uranium from recent anthropogenic DU deposit is weakly bound to soil aggregates and more mobile than geologically occurring natural uranium (NU). Moreover, 80% of uranium in leachates was located in the colloidal fractions. Nevertheless, the percentage of DU in the colloidal and dissolved fractions suggests that NU is mainly associated with the non-mobile coarser fractions of the soil. A field investigation revealed that the calculated percentages of DU in soil and groundwater samples result in the enhanced mobility of uranium downstream from the deposit area. Colloidal uranium represents between 10% and 32% of uranium in surface water and between 68% and 90% of uranium in groundwater where physicochemical parameters are similar to those of the leachates. Finally, as observed in batch leaching tests, the colloidal fractions of groundwater contain slightly less DU than the dissolved fraction, indicating that DU is primarily associated with macromolecules in dissolved fraction. (authors)

Use of gamma camera for measurement of the internal contamination with depleted uranium

International Nuclear Information System (INIS)

Spaic, R.; Markovic, S.; Pavlovic, S.; Pavlovic, R.; Ajdinovic, B.; Baskot, B.; Djurovic, B.

2000-01-01

Depleted uranium from radioactive wastes is used for manufacturing bullets used in Iraq, Republic of Serbia and Yugoslavia. These bullets are extremely dense and capable of penetrating heavily armored vehicles. Their medical importance lies in the fact that the bullets contain seventy percent depleted uranium which creates aerosolized particles less than five microns in diameter, small enough to be inhaled, after spontaneous bullet burn at impact. Nuclear medicine scientists must be aware of this and be prepared to measure internal contamination of persons exposed to this radioactive material. Whole body counters (WBC) represent appropriate equipment for this purpose but their availability in developing countries is not sufficient. Gamma camera is an alternative. The minimum detectable activity (MDA) of depleted uranium, iodine and technetium for gamma cameras was measured in this paper. Low energy X-ray 100 KeV with 20% windows are used for the depleted uranium detection. About 40% gamma emissions from depleted uranium fall within these limits. The activities measured (50-100 Bq) are about ten times higher then on WBC (5 Bq). This does not limit the use of gamma cameras for measurement of lung or whole body internal contamination with depleted uranium. (author)

The distribution of depleted uranium contamination in Colonie, NY, USA

International Nuclear Information System (INIS)

Lloyd, N.S.; Chenery, S.R.N.; Parrish, R.R.

2009-01-01

Uranium oxide particles were dispersed into the environment from a factory in Colonie (NY, USA) by prevailing winds during the 1960s and '70s. Uranium concentrations and isotope ratios from bulk soil samples have been accurately measured using inductively coupled plasma quadrupole mass spectrometry (ICP-QMS) without the need for analyte separation chemistry. The natural range of uranium concentrations in the Colonie soils has been estimated as 0.7-2.1 μg g -1 , with a weighted geometric mean of 1.05 μg g -1 ; the contaminated soil samples comprise uranium up to 500 ± 40 μg g -1 . A plot of 236 U/ 238 U against 235 U/ 238 U isotope ratios describes a mixing line between natural uranium and depleted uranium (DU) in bulk soil samples; scatter from this line can be accounted for by heterogeneity in the DU particulate. The end-member of DU compositions aggregated in these bulk samples comprises (2.05 ± 0.06) x 10 -3235 U/ 238 U, (3.2 ± 0.1) x 10 -5236 U/ 238 U, and (7.1 ± 0.3) x 10 -6234 U/ 238 U. The analytical method is sensitive to as little as 50 ng g -1 DU mixed with the natural uranium occurring in these soils. The contamination footprint has been mapped northward from site, and at least one third of the uranium in a soil sample from the surface 5 cm, collected 5.1 km NNW of the site, is DU. The distribution of contamination within the surface soil horizon follows a trend of exponential decrease with depth, which can be approximated by a simple diffusion model. Bioturbation by earthworms can account for dispersal of contaminant from the soil surface, in the form of primary uranium oxide particulates, and uranyl species that are adsorbed to organic matter. Considering this distribution, the total mass of uranium contamination emitted from the factory is estimated to be c. 4.8 tonnes.

The distribution of depleted uranium contamination in Colonie, NY, USA

Energy Technology Data Exchange (ETDEWEB)

Lloyd, N.S., E-mail: nsl3@alumni.leicester.ac.uk [Department of Geology, University of Leicester, University Road, Leicester, LE1 7RH (United Kingdom); Chenery, S.R.N. [British Geological Survey, Kingsley Dunham Centre, Keyworth, Nottingham, NG12 5GG (United Kingdom); Parrish, R.R. [Department of Geology, University of Leicester, University Road, Leicester, LE1 7RH (United Kingdom); NERC Isotope Geosciences Laboratory, Kingsley Dunham Centre, Keyworth, Nottingham, NG12 5GG (United Kingdom)

2009-12-20

Uranium oxide particles were dispersed into the environment from a factory in Colonie (NY, USA) by prevailing winds during the 1960s and '70s. Uranium concentrations and isotope ratios from bulk soil samples have been accurately measured using inductively coupled plasma quadrupole mass spectrometry (ICP-QMS) without the need for analyte separation chemistry. The natural range of uranium concentrations in the Colonie soils has been estimated as 0.7-2.1 {mu}g g{sup -1}, with a weighted geometric mean of 1.05 {mu}g g{sup -1}; the contaminated soil samples comprise uranium up to 500 {+-} 40 {mu}g g{sup -1}. A plot of {sup 236}U/{sup 238}U against {sup 235}U/{sup 238}U isotope ratios describes a mixing line between natural uranium and depleted uranium (DU) in bulk soil samples; scatter from this line can be accounted for by heterogeneity in the DU particulate. The end-member of DU compositions aggregated in these bulk samples comprises (2.05 {+-} 0.06) x 10{sup -3235}U/{sup 238}U, (3.2 {+-} 0.1) x 10{sup -5236}U/{sup 238}U, and (7.1 {+-} 0.3) x 10{sup -6234}U/{sup 238}U. The analytical method is sensitive to as little as 50 ng g{sup -1} DU mixed with the natural uranium occurring in these soils. The contamination footprint has been mapped northward from site, and at least one third of the uranium in a soil sample from the surface 5 cm, collected 5.1 km NNW of the site, is DU. The distribution of contamination within the surface soil horizon follows a trend of exponential decrease with depth, which can be approximated by a simple diffusion model. Bioturbation by earthworms can account for dispersal of contaminant from the soil surface, in the form of primary uranium oxide particulates, and uranyl species that are adsorbed to organic matter. Considering this distribution, the total mass of uranium contamination emitted from the factory is estimated to be c. 4.8 tonnes.

Study on depleted uranium at the airplane accident in Bijlmermeer, Amsterdam, Netherlands

International Nuclear Information System (INIS)

Veltkamp, A.C.; Van Hienen, J.F.A.

1998-09-01

The El Al airplane, which crashed in the urban area Bijlmermeer in Amsterdam, Netherlands, October 4th, 1992, contained balance weights of depleted uranium. Part of the balance weights has not been found after the disaster and its not sure what happened with the lost part. One of the options is that the uranium atomized during or after the fire. To clarify this the Dutch Civil Aviation Authority (RLD) ordered the Netherlands Energy Research Foundation (ECN) to study the fore-mentioned option on the basis of the following questions: (1) at which temperature will depleted uranium atomize and thus be released into the air?; (2) at which temperature will depleted uranium burn?; and (3) what is the chance that depleted uranium will atomize under the conditions as they occurred during the aircraft accident in the Bijlmermeer? The overall impression is that during the fire little if any uranium oxide has been released into the air. Because of lack of knowledge about the actual conditions, partial or complete oxidation can not be excluded with cast-iron certainty. 16 refs

Risks associated to the depleted uranium in the piercing shells

International Nuclear Information System (INIS)

2001-01-01

Following the complaints lodged by military personnel against the consequences of the utilization of depleted uranium in weapons during the Balkans war (1995-1999), the governments of six concerned countries asked information to the NATO. In this paper the IPSN gives its own opinion on this problem: the characteristics of the uranium and the depleted uranium, the impacts of the shell fires on the human and the environment. To establish the risks in terms of leukemia and the liabilities the IPSN advises more biological tests and more information on the shells utilization. (A.L.B.)

Depleted Uranium Hexafluoride Management Program. The technology assessment report for the long-term management of depleted uranium hexafluoride. Volume 2

International Nuclear Information System (INIS)

Zoller, J.N.; Rosen, R.S.; Holliday, M.A.

1995-01-01

With the publication of a Request for Recommendations and Advance Notice of Intent in the November 10, 1994 Federal Register, the Department of Energy initiated a program to assess alternative strategies for the long-term management or use of depleted uranium hexafluoride. This Request was made to help ensure that, by seeking as many recommendations as possible, Department management considers reasonable options in the long-range management strategy. The Depleted Uranium Hexafluoride Management Program consists of three major program elements: Engineering Analysis, Cost Analysis, and an Environmental Impact Statement. This Technology Assessment Report is the first part of the Engineering Analysis Project, and assesses recommendations from interested persons, industry, and Government agencies for potential uses for the depleted uranium hexafluoride stored at the gaseous diffusion plants in Paducah, Kentucky, and Portsmouth, Ohio, and at the Oak Ridge Reservation in Tennessee. Technologies that could facilitate the long-term management of this material are also assessed. The purpose of the Technology Assessment Report is to present the results of the evaluation of these recommendations. Department management will decide which recommendations will receive further study and evaluation

Depleted Uranium Hexafluoride Management Program. The technology assessment report for the long-term management of depleted uranium hexafluoride. Volume 2

Energy Technology Data Exchange (ETDEWEB)

Zoller, J.N.; Rosen, R.S.; Holliday, M.A. [and others

1995-06-30

With the publication of a Request for Recommendations and Advance Notice of Intent in the November 10, 1994 Federal Register, the Department of Energy initiated a program to assess alternative strategies for the long-term management or use of depleted uranium hexafluoride. This Request was made to help ensure that, by seeking as many recommendations as possible, Department management considers reasonable options in the long-range management strategy. The Depleted Uranium Hexafluoride Management Program consists of three major program elements: Engineering Analysis, Cost Analysis, and an Environmental Impact Statement. This Technology Assessment Report is the first part of the Engineering Analysis Project, and assesses recommendations from interested persons, industry, and Government agencies for potential uses for the depleted uranium hexafluoride stored at the gaseous diffusion plants in Paducah, Kentucky, and Portsmouth, Ohio, and at the Oak Ridge Reservation in Tennessee. Technologies that could facilitate the long-term management of this material are also assessed. The purpose of the Technology Assessment Report is to present the results of the evaluation of these recommendations. Department management will decide which recommendations will receive further study and evaluation.

Determination of natural and depleted uranium in urine at the ppt level: an interlaboratory analytical exercise

International Nuclear Information System (INIS)

D'Agostino, P.A.; Ough, E.A.; Glover, S.E.; Vallerand, A.L.

2002-10-01

An analytical exercise was initiated in order to determine those analytical procedures with the capacity to measure uranium isotope ratios ( 238 U/ 235 U) in urine samples containing less that 1μ uranium /L urine. A host laboratory was tasked with the preparation of six sets (12 samples per set) of synthetic urine samples spiked with varying amounts of natural and depleted (0.2% 235 U) uranium. The sets of samples contained total uranium in the range 25 ng U/L urine to 770 ng U/L urine, with isotope ratios ( 238 U/ 235 U) from 137.9 (natural uranium) to 215 (∼50% depleted uranium). Sets of samples were shipped to five testing laboratories (four Canadian and one European) for total and isotopic assay. The techniques employed in the analyses included sector field inductively coupled plasma mass spectrometry (ICP-SF-MS), quadrupole inductively coupled plasma mass spectrometry (ICP-Q-MS), thermal ionization mass spectrometry (TIMS) and neutron activation analysis (NAA). Full results were obtained from three testing labs (ICP-SF-MS, ICP-Q-MS and TIMS). Their results, plus partial results from the NAA lab, have been included in this report. Total uranium and isotope ratio results obtained from ICP-SF-MS and ICP-Q-MS were in good agreement with the host lab values. Neutron activation analysis and TIMS reported total uranium concentrations that differed from the host lab. An incomplete set of isotopic ratios was obtained from the NAA lab with some results reporting enriched uranium (% 235 U > 0.7). Based on the reported results, the four analytical procedures were ranked: ICP-SF-MS (1), ICP-Q-MS (2), TIMS (3) and NAA (4). (author)

Depleted uranium: an explosive dossier

International Nuclear Information System (INIS)

Barrillot, B.

2001-01-01

This book relates the history of depleted uranium, contemporaneous with the nuclear bomb history. Initially used in nuclear weapons and in experiments linked with nuclear weapons development, this material has been used also in civil industry, in particular in aeronautics. However, its properties made it interesting for military applications all along the 'cold war'. (J.S.)

Riddle of depleted uranium

International Nuclear Information System (INIS)

Hussein, A.S.

2005-01-01

Depleted Uranium (DU) is the waste product of uranium enrichment from the manufacturing of fuel rods for nuclear reactors in nuclear power plants and nuclear power ships. DU may also results from the reprocessing of spent nuclear reactor fuel. Potentially DU has both chemical and radiological toxicity with two important targets organs being the kidney and the lungs. DU is made into a metal and, due to its availability, low price, high specific weight, density and melting point as well as its pyrophoricity; it has a wide range of civilian and military applications. Due to the use of DU over the recent years, there appeared in some press on health hazards that are alleged to be due to DU. In these paper properties, applications, potential environmental and health effects of DU are briefly reviewed

Depleted uranium hexafluoride: The source material for advanced shielding systems

Energy Technology Data Exchange (ETDEWEB)

Quapp, W.J.; Lessing, P.A. [Idaho National Engineering Lab., Idaho Falls, ID (United States); Cooley, C.R. [Department of Technology, Germantown, MD (United States)

1997-02-01

The U.S. Department of Energy (DOE) has a management challenge and financial liability problem in the form of 50,000 cylinders containing 555,000 metric tons of depleted uranium hexafluoride (UF{sub 6}) that are stored at the gaseous diffusion plants. DOE is evaluating several options for the disposition of this UF{sub 6}, including continued storage, disposal, and recycle into a product. Based on studies conducted to date, the most feasible recycle option for the depleted uranium is shielding in low-level waste, spent nuclear fuel, or vitrified high-level waste containers. Estimates for the cost of disposal, using existing technologies, range between $3.8 and $11.3 billion depending on factors such as the disposal site and the applicability of the Resource Conservation and Recovery Act (RCRA). Advanced technologies can reduce these costs, but UF{sub 6} disposal still represents large future costs. This paper describes an application for depleted uranium in which depleted uranium hexafluoride is converted into an oxide and then into a heavy aggregate. The heavy uranium aggregate is combined with conventional concrete materials to form an ultra high density concrete, DUCRETE, weighing more than 400 lb/ft{sup 3}. DUCRETE can be used as shielding in spent nuclear fuel/high-level waste casks at a cost comparable to the lower of the disposal cost estimates. Consequently, the case can be made that DUCRETE shielded casks are an alternative to disposal. In this case, a beneficial long term solution is attained for much less than the combined cost of independently providing shielded casks and disposing of the depleted uranium. Furthermore, if disposal is avoided, the political problems associated with selection of a disposal location are also avoided. Other studies have also shown cost benefits for low level waste shielded disposal containers.

Decontamination of Cape Arza (Montenegro) from depleted Uranium

International Nuclear Information System (INIS)

Vukotich, P.; Kovachevich, M.; Vasich, V.; Ristich, N.

2002-01-01

On May 30, 1999, NATO A-10 aircrafts attacked Cape Arza, a very attractive touring area on peninsula Lustica, at the entrance of Boka Kotorska Bay, in Montenegro. They fired anti-armour rounds with penetrators made of depleted uranium. Such an armour-penetrating round has a length of 173 mm and a diameter of 30 mm. The bullet has an aluminium case (jacket) and inside it a conical DU penetrator. The length of the penetrator itself is 95 mm, and the diameter of its base is 16 mm. The penetrator weight is 292 g. According to the data reported by NATO (NATO, 2001), the total number of rounds fired against Cape Arza was 480. As to the data on combat mix of the A-10 aircraft gun, 300 (UNEP, 2001) or 400 (UNEP, 2001; FAS) of these rounds where with DU penetrators, and the rest with a classical charge. This means that Cape Arza was contaminated with 90 or 120 kg of DU, or with a radioactivity of (3.5 - 4.7) · 10 9 Bq. Depleted uranium is a waste product of the process of uranium enrichment in 2 35U isotope, for use in nuclear reactors or in nuclear weapons. The isotopic composition of depleted uranium is (Harley et al., 1999): (99.7 - 99.8) % of 2 38U , (0.2 - 0.3) % of 2 35U , 0.001 % of 2 34U , and only traces of 2 34T h, 2 34P a and 2 31T h. If traces of the isotopes 2 36U , 2 39P u and 2 40P u are also present, as it is the case with DU from Cape Arza (UNEP, 2002), the depleted uranium is obtained by reprocessing of spent nuclear reactor fuel. The activity concentration of depleted uranium is 39.42 · 10 6 Bq/kg. Most of it comes from 2 38U and its decay products 2 34T h and 2 34P a which are in radioactive equilibrium (12.27 · 10 6 Bq/kg per each of them), and the less part from 2 35U and 2 31T h (0.16 · 10 6 Bq/kg per each) (UNEP, 1999), while the activity concentration of 2 36U , 2 39P u and 2 40P u is below 100 Bq/kg (UNEP, 2001)

Health and environmental problems of using depleted uranium

International Nuclear Information System (INIS)

Matousek, J.

2006-01-01

In the 1970's, a core of depleted uranium (DU) began to be introduced into the break through anti-tank munitions to enhance their effectiveness. The health and environmental threats of DU stem from the pyrophoric character of the core, burnt when penetrating armour to an aerosol of uranium oxides deposited in tissues after inhalation or ingestion. Their delayed effects are due to internal alpha irradiation by daughter products and toxicity of uranium. (authors)

Radiological contamination by depleted uranium in the Al-Tahreer tower building

International Nuclear Information System (INIS)

Al-Ataby, N.R.; Aisa, B.H.; Jebir, H.M.; Hatem, J.N.

2011-01-01

The research plan included assessment of the radioactivity of the Al-Tahreer Tower Building (the Turkish restaurant recent) through direct measurements and sampling of soil for the four floors (1th,2th,3th,4th) of the building, which contains fourteen floor in addition to the basement, by using portable radiation detection equipment to know the increasing in the levels of exposure and contamination resulting from the bombing a Al-Tahreer Tower building by depleted uranium bullets, the results of radiological surveys by using the portable contamination radiation detection (CAB) indicated readings of contaminated soil reached to 60 c/sec, and parts of shells of depleted uranium reached to 90 c/ sec , while the natural contamination rate in the area is (0.5 c/sec), the natural exposure rate in the area is 9 μR/ hr but the higher exposure rate reached to 60 μR / hr when the device (Ludlum) putting on the contaminated regions(distance about 0.5 cm). The radiological analyses of the collected soil samples were done in the laboratory of the center of Radiological Researches in the Ministry of sciences and Technology by using gamma spectrometry (which contains High-purity Germanium Detector) with a efficiency of 40% and resolution 2 keV for Energy, 1.33 Mev,collection,preparations and tests of soil samples were all done according to IAEA.The normal concentration for Th 234 and Pa 234 m in the soil samples taken from areas near to the building (can consider as background radiation region) is in range 41 Bq /Kg for Th 234 ,and nil for pa 234 m ,while higher concentration of Th 234 in contaminated soil is 1194 Bq/kg,and 1664 Bq/kg for pa 234 m which is a clear indication of the presence of high concentrations an isotope of uranium 238 as they are supposed to be in equilibrium radiation. The major aim of this study include removal the contaminated regions in the building, to protect the population and the environment from the effect of radiological contamination which

Depleted uranium hexafluoride management program : data compilation for the Paducah site

International Nuclear Information System (INIS)

Hartmann, H.

2001-01-01

This report is a compilation of data and analyses for the Paducah site, near Paducah, Kentucky. The data were collected and the analyses were done in support of the U.S. Department of Energy (DOE) 1999 Programmatic Environmental Impact Statement for Alternative Strategies for the Long-Term Management and Use of Depleted Uranium Hexafluoride (DOE/EIS-0269). The report describes the affected environment at the Paducah site and summarizes potential environmental impacts that could result from conducting the following depleted uranium hexafluoride (UF 6 ) activities at the site: continued cylinder storage, preparation of cylinders for shipment, conversion, and long-term storage. DOE's preferred alternative is to begin converting the depleted UF 6 inventory as soon as possible to either uranium oxide, uranium metal, or a combination of both, while allowing for use of as much of this inventory as possible

Depleted uranium hexafluoride management program : data compilation for the Portsmouth site

International Nuclear Information System (INIS)

Hartmann, H. M.

2001-01-01

This report is a compilation of data and analyses for the Portsmouth site, near Portsmouth, Ohio. The data were collected and the analyses were done in support of the U.S. Department of Energy (DOE) 1999 Programmatic Environmental Impact Statement for Alternative Strategies for the Long-Term Management and Use of Depleted Uranium Hexafluoride (DOE/EIS-0269). The report describes the affected environment at the Portsmouth site and summarizes potential environmental impacts that could result from conducting the following depleted uranium hexafluoride (UF 6 ) management activities at the site: continued cylinder storage, preparation of cylinders for shipment, conversion, and long-term storage. DOE's preferred alternative is to begin converting the depleted UF 6 inventory as soon as possible to either uranium oxide, uranium metal, or a combination of both, while allowing for use of as much of this inventory as possible

Selection of a management strategy for depleted uranium

International Nuclear Information System (INIS)

Patton, S.; Hanrahan, E.; Bradley, C. Jnr.

1995-01-01

A consequence of the uranium enrichment process is the accumulation of a significant amount of depleted uranium hexafluoride (UF 6 ). Currently, in the United States approximately 560 000 tonnes of the material are stored at three different sites. The US Department of Energy (DOE) has recently initiated a programme to consider alternative strategies for the cost-effective and environmentally safe long-term management of this inventory of depleted UF 6 . The programme involves a technology and engineering assessment of proposed management options (which are: use/reuse, conversion, storage, or disposal) and an analysis of the potential environmental impacts and life-cycle costs of alternative management strategies. The information obtained from the studies will be used by the DOE to select a preferred long-term management strategy. Because of its provisions for considering a wide range of relevant issues and involving the public, this programme has become a model for future DOE materials disposition programmes. This paper presents an overview of the Depleted Uranium Hexafluoride Management Programme. Technical findings of the programme to date are presented, and major issues involved in selecting and implementing a management strategy are discussed. (author)

Separation and recovery method for depleted uranium from spent fuel

International Nuclear Information System (INIS)

Imoto, Yoshie; Fujita, Reiko.

1993-01-01

Spent oxide fuels are reduced in a molten salt of CaCl 2 -CaF 2 to convert them into metals, then melted in an Fe-U bath disposed in an electrolytic refining vessel and brought into contact with molten Mg, to extract transuranium elements and rare earth elements contained in the Fe-U bath as metals in the molten Mg. Then molten Mg is removed and the residue is brought into contact with KCl-LiCl molten salt and electrolyzed using the Fe-U as an anode. Then, uranium is recovered by deposition on an iron cathode disposed in chloride electrolytes of the electrolytic refining vessel. Uranium and transuranium elements can be thus separated and, for example, depleted uranium for use in blanket fuels can be recovered easily. This can greatly reduce the temporary storage amount of depleted uranium, to eliminate requirement for a large-scaled facility used exclusively for storing uranium and long time management for uranium. (T.M.)

Depleted Uranium Hexafluoride Management Program. The technology assessment report for the long-term management of depleted uranium hexafluoride. Volume 1

Energy Technology Data Exchange (ETDEWEB)

Zoller, J.N.; Rosen, R.S.; Holliday, M.A. [and others

1995-06-30

With the publication of a Request for Recommendations and Advance Notice of Intent in the November 10, 1994 Federal Register, the Department of Energy initiated a program to assess alternative strategies for the long-term management or use of depleted uranium hexafluoride. This Request was made to help ensure that, by seeking as many recommendations as possible, Department management considers reasonable options in the long-range management strategy. The Depleted Uranium Hexafluoride Management Program consists of three major program elements: Engineering Analysis, Cost Analysis, and an Environmental Impact Statement. This Technology Assessment Report is the first part of the Engineering Analysis Project, and assesses recommendations from interested persons, industry, and Government agencies for potential uses for the depleted uranium hexafluoride stored at the gaseous diffusion plants in Paducah, Kentucky, and Portsmouth, Ohio, and at the Oak Ridge Reservation in Tennessee. Technologies that could facilitate the long-term management of this material are also assessed. The purpose of the Technology Assessment Report is to present the results of the evaluation of these recommendations. Department management will decide which recommendations will receive further study and evaluation. These Appendices contain the Federal Register Notice, comments on evaluation factors, independent technical reviewers resumes, independent technical reviewers manual, and technology information packages.

Depleted Uranium Hexafluoride Management Program. The technology assessment report for the long-term management of depleted uranium hexafluoride. Volume 1

International Nuclear Information System (INIS)

Zoller, J.N.; Rosen, R.S.; Holliday, M.A.

1995-01-01

With the publication of a Request for Recommendations and Advance Notice of Intent in the November 10, 1994 Federal Register, the Department of Energy initiated a program to assess alternative strategies for the long-term management or use of depleted uranium hexafluoride. This Request was made to help ensure that, by seeking as many recommendations as possible, Department management considers reasonable options in the long-range management strategy. The Depleted Uranium Hexafluoride Management Program consists of three major program elements: Engineering Analysis, Cost Analysis, and an Environmental Impact Statement. This Technology Assessment Report is the first part of the Engineering Analysis Project, and assesses recommendations from interested persons, industry, and Government agencies for potential uses for the depleted uranium hexafluoride stored at the gaseous diffusion plants in Paducah, Kentucky, and Portsmouth, Ohio, and at the Oak Ridge Reservation in Tennessee. Technologies that could facilitate the long-term management of this material are also assessed. The purpose of the Technology Assessment Report is to present the results of the evaluation of these recommendations. Department management will decide which recommendations will receive further study and evaluation. These Appendices contain the Federal Register Notice, comments on evaluation factors, independent technical reviewers resumes, independent technical reviewers manual, and technology information packages

Depleted and natural uranium: chemistry and toxicological effects.

Science.gov (United States)

Craft, Elena; Abu-Qare, Aquel; Flaherty, Meghan; Garofolo, Melissa; Rincavage, Heather; Abou-Donia, Mohamed

2004-01-01

Depleted uranium (DU) is a by-product from the chemical enrichment of naturally occurring uranium. Natural uranium is comprised of three radioactive isotopes: (238)U, (235)U, and (234)U. This enrichment process reduces the radioactivity of DU to roughly 30% of that of natural uranium. Nonmilitary uses of DU include counterweights in airplanes, shields against radiation in medical radiotherapy units and transport of radioactive isotopes. DU has also been used during wartime in heavy tank armor, armor-piercing bullets, and missiles, due to its desirable chemical properties coupled with its decreased radioactivity. DU weapons are used unreservedly by the armed forces. Chemically and toxicologically, DU behaves similarly to natural uranium metal. Although the effects of DU on human health are not easily discerned, they may be produced by both its chemical and radiological properties. DU can be toxic to many bodily systems, as presented in this review. Most importantly, normal functioning of the kidney, brain, liver, and heart can be affected by DU exposure. Numerous other systems can also be affected by DU exposure, and these are also reviewed. Despite the prevalence of DU usage in many applications, limited data exist regarding the toxicological consequences on human health. This review focuses on the chemistry, pharmacokinetics, and toxicological effects of depleted and natural uranium on several systems in the mammalian body. A section on risk assessment concludes the review.

Uranium under its depleted state

International Nuclear Information System (INIS)

2001-01-01

This day organised by the SFRP, with the help of the Army Health service, the service of radiation protection of Army and IPSN is an information day to inform the public about the real toxicity of uranium, and its becoming in man and environment, about the risks during the use of depleted uranium and eventual consequences of its dispersion after a conflict, to give information on how is managed the protection of workers (civil or military ones) and what is really the situation of French military personnel in these conflicts. The news have brought to the shore cases of leukemia it is necessary to bring some information to the origin of this disease. (N.C.)

The consequences and hazards of depleted uranium weapons used by US army since gulf war

International Nuclear Information System (INIS)

Mao Yongze

1999-01-01

Military equipment and development of depleted uranium weapon in USA, the depleted uranium weapon used in gulf war by USA army, personnel irradiation in the gulf war, and the protection in the gulf war are introduced. The radioactivity, radioactive characteristics, chemical toxicity and hazard of the depleted uranium are also introduced

The health hazards of depleted uranium munitions. Part 1

International Nuclear Information System (INIS)

2001-01-01

Depleted uranium is a toxic and weakly radioactive metal used for a variety of purposes. Perhaps its most controversial use is in battlefield munitions, where it can be widely dispersed in the form of fine particles and shrapnel that may enter the bodies of combatants and others through inhalation, ingestion or wounding. It is a matter of legitimate public concern whether the use of this material in this way could create unacceptable health hazards or damage to the environment. The objective of our study has been to provide the best scientific understanding of the ways in which the material may be distributed, how it may be taken up by humans, and the potential implications for health. For politicians, any hazards to health have to be balanced against the military advantages that the use of these munitions confers. We have not tried to reach a judgment on these political issues, but we believe that a better scientific understanding of the extent of the hazards will make it easier for these wider questions to be addressed in a more objective way. This report is the first of two, and addresses the likely levels of exposure to depleted uranium, the resulting radiological risks, and the lessons to be learned from epidemiological studies. Our second report will address toxicological risks and environmental issues. So far, we conclude that risks from radiation are low for most soldiers on the battlefield, and for civilians who later return to the area. However, there are uncertainties about the maximal levels of exposure to depleted uranium on the battlefield, and there may be circumstances in which a few soldiers are exposed to levels of depleted uranium that result in a significant risk to health. Further studies are needed to determine the levels of exposure to depleted uranium that might occur on the battlefield and to judge whether such higher risks are likely to occur in practice

Operating experience in processing of differently sourced deeply depleted uranium oxide and production of deeply depleted uranium metal ingots

International Nuclear Information System (INIS)

Manna, S.; Ladola, Y.S.; Sharma, S.; Chowdhury, S.; Satpati, S.K.; Roy, S.B.

2009-01-01

Uranium Metal Plant (UMP) of BARC had first time experience on production of three Depleted Uranium Metal (DUM) ingots of 76kg, 152kg and 163kg during March 1991. These ingots were produced by processing depleted uranyl nitrate solution produced at Plutonium Plant (PP), Trombay. In recent past Uranium Metal Plant (UMP), Uranium Extraction Division (UED), has been assigned to produce tonnage quantity of Deeply DUM (DDUM) from its oxide obtained from PP, PREFRE and RMP, BARC. This is required for shielding the high radioactive source of BHABHATRON Tele-cobalt machine, which is used for cancer therapy. The experience obtained in processing of various DDU oxides is being utilized for design of large scale DDU-metal plant under XIth plan project. The physico- chemical characteristics like morphology, density, flowability, reactivity, particle size distribution, which are having direct effect on reactivity of the powders of the DDU oxide powder, were studied and the shop-floor operational experience in processing of different oxide powder were obtained and recorded. During campaign trials utmost care was taken to standardized all operating conditions using the same equipment which are in use for natural uranium materials processing including safety aspects both with respect to radiological safety and industrial safety. Necessary attention and close monitoring were specially arranged and maintained for the safety aspects during the trial period. In-house developed pneumatic transport system was used for powder transfer and suitable dust arresting system was used for reduction of powder carry over

Depleted uranium disposal options evaluation

International Nuclear Information System (INIS)

Hertzler, T.J.; Nishimoto, D.D.; Otis, M.D.

1994-05-01

The Department of Energy (DOE), Office of Environmental Restoration and Waste Management, has chartered a study to evaluate alternative management strategies for depleted uranium (DU) currently stored throughout the DOE complex. Historically, DU has been maintained as a strategic resource because of uses for DU metal and potential uses for further enrichment or for uranium oxide as breeder reactor blanket fuel. This study has focused on evaluating the disposal options for DU if it were considered a waste. This report is in no way declaring these DU reserves a ''waste,'' but is intended to provide baseline data for comparison with other management options for use of DU. To PICS considered in this report include: Retrievable disposal; permanent disposal; health hazards; radiation toxicity and chemical toxicity

Depleted uranium instead of lead in munitions: the lesser evil.

Science.gov (United States)

Jargin, Sergei V

2014-03-01

Uranium has many similarities to lead in its exposure mechanisms, metabolism and target organs. However, lead is more toxic, which is reflected in the threshold limit values. The main potential hazard associated with depleted uranium is inhalation of the aerosols created when a projectile hits an armoured target. A person can be exposed to lead in similar ways. Accidental dangerous exposures can result from contact with both substances. Encountering uranium fragments is of minor significance because of the low penetration depth of alpha particles emitted by uranium: they are unable to penetrate even the superficial keratin layer of human skin. An additional cancer risk attributable to the uranium exposure might be significant only in case of prolonged contact of the contaminant with susceptible tissues. Lead intoxication can be observed in the wounded, in workers manufacturing munitions etc; moreover, lead has been documented to have a negative impact on the intellectual function of children at very low blood concentrations. It is concluded on the basis of the literature overview that replacement of lead by depleted uranium in munitions would be environmentally beneficial or largely insignificant because both lead and uranium are present in the environment.

Depleted uranium instead of lead in munitions: the lesser evil

International Nuclear Information System (INIS)

Jargin, Sergei V

2014-01-01

Uranium has many similarities to lead in its exposure mechanisms, metabolism and target organs. However, lead is more toxic, which is reflected in the threshold limit values. The main potential hazard associated with depleted uranium is inhalation of the aerosols created when a projectile hits an armoured target. A person can be exposed to lead in similar ways. Accidental dangerous exposures can result from contact with both substances. Encountering uranium fragments is of minor significance because of the low penetration depth of alpha particles emitted by uranium: they are unable to penetrate even the superficial keratin layer of human skin. An additional cancer risk attributable to the uranium exposure might be significant only in case of prolonged contact of the contaminant with susceptible tissues. Lead intoxication can be observed in the wounded, in workers manufacturing munitions etc; moreover, lead has been documented to have a negative impact on the intellectual function of children at very low blood concentrations. It is concluded on the basis of the literature overview that replacement of lead by depleted uranium in munitions would be environmentally beneficial or largely insignificant because both lead and uranium are present in the environment. (opinion)

A modern depleted uranium manufacturing facility

International Nuclear Information System (INIS)

Zagula, T.A.

1995-07-01

The Specific Manufacturing Capabilities (SMC) Project located at the Idaho National Engineering Laboratory (INEL) and operated by Lockheed Martin Idaho Technologies Co. (LMIT) for the Department of Energy (DOE) manufactures depleted uranium for use in the U.S. Army MIA2 Abrams Heavy Tank Armor Program. Since 1986, SMC has fabricated more than 12 million pounds of depleted uranium (DU) products in a multitude of shapes and sizes with varying metallurgical properties while maintaining security, environmental, health and safety requirements. During initial facility design in the early 1980's, emphasis on employee safety, radiation control and environmental consciousness was gaining momentum throughout the DOE complex. This fact coupled with security and production requirements forced design efforts to focus on incorporating automation, local containment and computerized material accountability at all work stations. The result was a fully automated production facility engineered to manufacture DU armor packages with virtually no human contact while maintaining security, traceability and quality requirements. This hands off approach to handling depleted uranium resulted in minimal radiation exposures and employee injuries. Construction of the manufacturing facility was complete in early 1986 with the first armor package certified in October 1986. Rolling facility construction was completed in 1987 with the first certified plate produced in the fall of 1988. Since 1988 the rolling and manufacturing facilities have delivered more than 2600 armor packages on schedule with 100% final product quality acceptance. During this period there was an annual average of only 2.2 lost time incidents and a single individual maximum radiation exposure of 150 mrem. SMC is an example of designing and operating a facility that meets regulatory requirements with respect to national security, radiation control and personnel safety while achieving production schedules and product quality

A review of the environmental behavior of uranium derived from depleted uranium alloy penetrators

Energy Technology Data Exchange (ETDEWEB)

Erikson, R.L.; Hostetler, C.J.; Divine, J.R.; Price, K.R.

1990-01-01

The use of depleted uranium (DU) penetrators as armor-piercing projectiles in the field results in the release of uranium into the environment. Elevated levels of uranium in the environment are of concern because of radioactivity and chemical toxicity. In addition to the direct contamination of the soil with uranium, the penetrators will also chemically react with rainwater and surface water. Uranium may be oxidized and leached into surface water or groundwater and may subsequently be transported. In this report, we review some of the factors affecting the oxidation of the DU metal and the factors influencing the leaching and mobility of uranium through surface water and groundwater pathways, and the uptake of uranium by plants growing in contaminated soils. 29 refs., 10 figs., 3 tabs.

Depleted uranium in the food chain at south of Iraq

International Nuclear Information System (INIS)

Al-Kiani, A. T.

2006-01-01

Depleted Uranium (D U) is uranium with low content of 2351) produced as a result of uranium enrichment. Du has high density (19.05 g/c m 3 ), which is 2.54 more than Iron, so it's high penetrating power makes it preferable as emanations with high penetration power. It was used in second Gulf ware in 1991 for first time. The radioactivity of soil, plants, fruit, meat, milk and water is measured using gamma ray spectroscopy. Materials and Methods: One hundred samples of soil, plants and tomato fruit were selected from the tomato farms near Basra city south of Iraq and 6 control samples from other farms not contaminated with depleted uranium (Du). Also samples of meats, milk and water were collected in January 2003. Radioactivity of these samples was measured using Gamma-ray spectrograph system with high purity Germanium detector with resolution of 2.2 keV at the energy of 1332.3 keV of Co-60. The system is connected to P C Pentium 111 with PCA program. Results: The measurements show that radiation equilibrium between 2 34T h and 2 26R existed with the range between (0.86-1.16) in uncontaminated soil samples. For contaminated soil samples radiation equilibrium between 2 34T h and Pa-234m existed with the range between (0.928- 0.956). The mathematical equations of Kosovo team were used. Results show that the soils of two farms were contaminated with (D U). The radioactivity of 2 26R for plants ranging from 5.97 to 7.26 and for tomato fruits samples between 9.16 to 12.4 Bq/kg. Comparing these values with the control radioactivity which range between 6.25 to 7.34 for fruits and 13.3 to 13.9 Bq/kg for plants indicate that these samples were not contaminated with D U. Conclusion: The soil samples of two farms were contaminated with D U but the fruit of these farms was not contaminated with D U may be due to its high molecular weight and not being water soluble. The radioactivity of 2 26R for different kinds of meat and milk for animal grazing near destroyed tanks

Comparison of two lung clearance models based on the dissolution rates of oxidized depleted uranium

Energy Technology Data Exchange (ETDEWEB)

Crist, K.C.

1984-10-01

An in-vitro dissolution study was conducted on two respirable oxidized depleted uranium samples. The dissolution rates generated from this study were then utilized in the International Commission on Radiological Protection Task Group lung clearance model and a lung clearance model proposed by Cuddihy. Predictions from both models based on the dissolution rates of the amount of oxidized depleted uranium that would be cleared to blood from the pulmonary region following an inhalation exposure were compared. It was found that the predictions made by both models differed considerably. The difference between the predictions was attributed to the differences in the way each model perceives the clearance from the pulmonary region. 33 references, 11 figures, 9 tables.

Comparison of two lung clearance models based on the dissolution rates of oxidized depleted uranium

International Nuclear Information System (INIS)

Crist, K.C.

1984-10-01

An in-vitro dissolution study was conducted on two respirable oxidized depleted uranium samples. The dissolution rates generated from this study were then utilized in the International Commission on Radiological Protection Task Group lung clearance model and a lung clearance model proposed by Cuddihy. Predictions from both models based on the dissolution rates of the amount of oxidized depleted uranium that would be cleared to blood from the pulmonary region following an inhalation exposure were compared. It was found that the predictions made by both models differed considerably. The difference between the predictions was attributed to the differences in the way each model perceives the clearance from the pulmonary region. 33 references, 11 figures, 9 tables

DUPoly process for treatment of depleted uranium and production of beneficial end products

International Nuclear Information System (INIS)

Kalb, P.D.; Adams, J.W.; Lageraaen, P.R.; Cooley, C.R.

2000-01-01

The present invention provides a process of encapsulating depleted uranium by forming a homogeneous mixture of depleted uranium and molten virgin or recycled thermoplastic polymer into desired shapes. Separate streams of depleted uranium and virgin or recycled thermoplastic polymer are simultaneously subjected to heating and mixing conditions. The heating and mixing conditions are provided by a thermokinetic mixer, continuous mixer or an extruder and preferably by a thermokinetic mixer or continuous mixer followed by an extruder. The resulting DUPoly shapes can be molded into radiation shielding material or can be used as counter weights for use in airplanes, helicopters, ships, missiles, armor or projectiles

Depleted uranium in environmental samples from Kuwait areas affected by the 1991 Gulf War

Energy Technology Data Exchange (ETDEWEB)

Danesi, P.R.; Burns, K.; Campbell, M.; Makarewicz, M.; Moreno, J.; Radecki, Z.; Cabianca, T.; Burkart, W. [International Atomic Energy Agency Vienna (Austria)

2004-07-01

Top soils (0-5 cm), soil profiles (0-35 cm), water and vegetation samples collected in several locations of Kuwait considered relevant by the local authorities either because fighting took place in or around them or important from the public reassurance point of view (residential areas, presence of farms or drinking water wells) were investigated for the presence of depleted uranium (DU) by inductively coupled plasma mass spectrometry and alpha and beta gamma spectrometry. More than 200 samples were collected and analysed. The measurements were subjected to rigorous quality assurance and control procedures and the uncertainties carefully evaluated. The results indicated that: (a) in the urban areas only natural uranium was present in the soil, (b) in the farming areas soil, vegetable and brackish water from wells also contained uranium at concentrations of no radiological significance, (c) at the only place where drinking water is extracted from a water body at a depth of about 50 m (this is bottled and locally consumed) no DU was present, (d) along and around the main road to Iraq, were a long retreating convoy was destroyed in 1991, no DU residues are now present, (e) in the oil field south of Kuwait City, that were severely hit by DU ammunition, DU penetrators can still be found and there are spots (generally just below corroded penetrators) where DU concentration in soil can reach up to 50,000 or 100,000 Bq/kg, (f) in the places were the many vehicles hit by DU ammunition were temporarily stored after the war only one spot containing some DU in soil (41 Bq/kg) was identified, (g) at the site where accidentally a fire broke out in 1991 in a US military depot storing a large quantity of DU munitions, only a few top soil spots containing low quantities ({approx} 90 Bq/kg) of DU were identified; the low DU concentration is the result of the cleaning conduced immediately after the explosion by the US forces and later on by the Kuwaiti authorities, and the complete

Depleted uranium in environmental samples from Kuwait areas affected by the 1991 Gulf War

International Nuclear Information System (INIS)

Danesi, P.R.; Burns, K.; Campbell, M.; Makarewicz, M.; Moreno, J.; Radecki, Z.; Cabianca, T.; Burkart, W.

2004-01-01

Top soils (0-5 cm), soil profiles (0-35 cm), water and vegetation samples collected in several locations of Kuwait considered relevant by the local authorities either because fighting took place in or around them or important from the public reassurance point of view (residential areas, presence of farms or drinking water wells) were investigated for the presence of depleted uranium (DU) by inductively coupled plasma mass spectrometry and alpha and beta gamma spectrometry. More than 200 samples were collected and analysed. The measurements were subjected to rigorous quality assurance and control procedures and the uncertainties carefully evaluated. The results indicated that: (a) in the urban areas only natural uranium was present in the soil, (b) in the farming areas soil, vegetable and brackish water from wells also contained uranium at concentrations of no radiological significance, (c) at the only place where drinking water is extracted from a water body at a depth of about 50 m (this is bottled and locally consumed) no DU was present, (d) along and around the main road to Iraq, were a long retreating convoy was destroyed in 1991, no DU residues are now present, (e) in the oil field south of Kuwait City, that were severely hit by DU ammunition, DU penetrators can still be found and there are spots (generally just below corroded penetrators) where DU concentration in soil can reach up to 50,000 or 100,000 Bq/kg, (f) in the places were the many vehicles hit by DU ammunition were temporarily stored after the war only one spot containing some DU in soil (41 Bq/kg) was identified, (g) at the site where accidentally a fire broke out in 1991 in a US military depot storing a large quantity of DU munitions, only a few top soil spots containing low quantities (∼ 90 Bq/kg) of DU were identified; the low DU concentration is the result of the cleaning conduced immediately after the explosion by the US forces and later on by the Kuwaiti authorities, and the complete

Measuring Aerosols Generated Inside Armoured Vehicles Perforated by Depleted Uranium Ammunition

International Nuclear Information System (INIS)

Parkhurst, MaryAnn

2003-01-01

In response to questions raised after the Gulf War about the health significance of exposure to depleted uranium (DU), the U.S. Department of Defense initiated a study designed to provide an improved scientific basis for assessment of possible health effects of soldiers in vehicles struck by these munitions. As part of this study, a series of DU penetrators were fired at an Abrams tank and a Bradley fighting vehicle, and the aerosols generated by vehicle perforation were collected and characterized. A robust sampling system was designed to collect aerosols in this difficult environment and to monitor continuously the sampler flow rates. Interior aerosols collected were analyzed for uranium concentration and particle size distribution as a function of time. They were also analyzed for uranium oxide phases, particle morphology, and dissolution in vitro. These data will provide input for future prospective and retrospective dose and health risk assessments of inhaled or ingested DU aerosols. This paper briefly discusses the target vehicles, firing trajectories, aerosol samplers and instrumentation control systems, and the types of analyses conducted on the samples

Depleted uranium: Metabolic disruptor?; Uranium appauvri: perturbateur metabolique?

Energy Technology Data Exchange (ETDEWEB)

Souidi, Maamar; Dublineau, Isabelle; Lestaevel, Philippe [Institut de Radioprotection et de Surete Nucleaire - IRSN, Direction de la radioprotection de l' homme, Laboratoire de radiotoxicologie experimentale, Service de radiobiologie et d' epidemiologie, BP 17, 92262 Fontenay-aux-Roses cedex (France)

2011-11-15

The presence of uranium in the environment can lead to long-term contamination of the food chain and of water intended for human consumption and thus raises many questions about the scientific and societal consequences of this exposure on population health. Although the biological effects of chronic low-level exposure are poorly understood, results of various recent studies show that contamination by depleted uranium (DU) induces subtle but significant biological effects at the molecular level in organs including the brain, liver, kidneys and testicles. For the first time, it has been demonstrated that DU induces effects on several metabolic pathways, including those metabolizing vitamin D, cholesterol, steroid hormones, acetylcholine and xenobiotics. This evidence strongly suggests that DU might well interfere with many metabolic pathways. It might thus contribute, together with other man-made substances in the environment, to increased health risks in some regions. (authors)

Effects of drop testing on scale model shipping containers shielded with depleted uranium

International Nuclear Information System (INIS)

Butler, T.A.

1980-02-01

Three scale model shipping containers shielded with depleted uranium were dropped onto an essentially unyielding surface from various heights to determine their margins to failure. This report presents the results of a thorough posttest examination of the models to check for basic structural integrity, shielding integrity, and deformations. Because of unexpected behavior exhibited by the depleted uranium shielding, several tests were performed to further characterize its mechanical properties. Based on results of the investigations, recommendations are made for improved container design and for applying the results to full-scale containers. Even though the specimens incorporated specific design features, the results of this study are generally applicable to any container design using depleted uranium

Uranium and the use of depleted uranium in weaponry; L'uranium et les armes a l'uranium appauvri

Energy Technology Data Exchange (ETDEWEB)

Roussel, R

2000-07-01

In this brief report the author shows that the use of shells involving a load of depleted uranium might lead to lasting hazards to civil population and environment. These hazards come from the part of the shell that has been dispersed as contaminating radioactive dusts. The author describes some features of radioactivity and highlights the role of Uranium-238 as a provider of energy to the planet. (A.C.)

Plutonium in depleted uranium penetrators

International Nuclear Information System (INIS)

McLaughlin, J.P.; Leon-Vintro, L.; Smith, K.; Mitchell, P.I.; Zunic, Z.S.

2002-01-01

Depleted Uranium (DU) penetrators used in the recent Balkan conflicts have been found to be contaminated with trace amounts of transuranic materials such as plutonium. This contamination is usually a consequence of DU fabrication being carried out in facilities also using uranium recycled from spent military and civilian nuclear reactor fuel. Specific activities of 239+240 Plutonium generally in the range 1 to 12 Bq/kg have been found to be present in DU penetrators recovered from the attack sites of the 1999 NATO bombardment of Kosovo. A DU penetrator recovered from a May 1999 attack site at Bratoselce in southern Serbia and analysed by University College Dublin was found to contain 43.7 +/- 1.9 Bq/kg of 239+240 Plutonium. This analysis is described. An account is also given of the general population radiation dose implications arising from both the DU itself and from the presence of plutonium in the penetrators. According to current dosimetric models, in all scenarios considered likely ,the dose from the plutonium is estimated to be much smaller than that due to the uranium isotopes present in the penetrators. (author)

Selection of a management strategy for depleted uranium hexafluoride

International Nuclear Information System (INIS)

Patton, S.E.; Hanrahan, E.J.; Bradley, C.E.

1995-01-01

A consequence of the uranium enrichment process used in the United States (US) is the accumulation of a significant amount of depleted uranium hexafluoride (UF 6 ). Currently, approximately 560,000 metric tons of the material are stored at three different sites. The US Department of Energy (DOE) has recently initiated a program to consider alternative strategies for the cost-effective and environmentally safe long-term management of this inventory of depleted UF 6 . The program involves a technology and engineering assessment of proposed management options (use/reuse, conversion, storage, or disposal) and an analysis of the potential environmental impacts and life-cycle costs of alternative management strategies. The information obtained from the studies will be used by the DOE to select a preferred long-term management strategy. The selection and implementation of a management strategy will involve consideration of a number of important issues such as environmental, health, and safety effects; the balancing of risks versus costs in a context of reduced government spending; socioeconomic implications, including effects on the domestic and international uranium industry; the technical status of proposed uses or technologies; and public involvement in the decision making process. Because of its provisions for considering a wide range of relevant issues and involving the public, this program has become a model for future DOE materials disposition programs. This paper presents an overview of the Depleted Uranium Hexafluoride Management Program. Technical findings of the program to date are presented, and major issues involved in selecting and implementing a management strategy are discussed

Physicochemical characterization of Capstone depleted uranium aerosols I: uranium concentration in aerosols as a function of time and particle size.

Science.gov (United States)

Parkhurst, Mary Ann; Cheng, Yung Sung; Kenoyer, Judson L; Traub, Richard J

2009-03-01

During the Capstone Depleted Uranium (DU) Aerosol Study, aerosols containing DU were produced inside unventilated armored vehicles (i.e., Abrams tanks and Bradley Fighting Vehicles) by perforation with large-caliber DU penetrators. These aerosols were collected and characterized, and the data were subsequently used to assess human health risks to personnel exposed to DU aerosols. The DU content of each aerosol sample was first quantified by radioanalytical methods, and selected samples, primarily those from the cyclone separator grit chambers, were analyzed radiochemically. Deposition occurred inside the vehicles as particles settled on interior surfaces. Settling rates of uranium from the aerosols were evaluated using filter cassette samples that collected aerosol as total mass over eight sequential time intervals. A moving filter was used to collect aerosol samples over time, particularly within the first minute after a shot. The results demonstrate that the peak uranium concentration in the aerosol occurred in the first 10 s after perforation, and the concentration decreased in the Abrams tank shots to about 50% within 1 min and to less than 2% after 30 min. The initial and maximum uranium concentrations were lower in the Bradley vehicle than those observed in the Abrams tank, and the concentration levels decreased more slowly. Uranium mass concentrations in the aerosols as a function of particle size were evaluated using samples collected in a cyclone sampler, which collected aerosol continuously for 2 h after perforation. The percentages of uranium mass in the cyclone separator stages ranged from 38 to 72% for the Abrams tank with conventional armor. In most cases, it varied with particle size, typically with less uranium associated with the smaller particle sizes. Neither the Abrams tank with DU armor nor the Bradley vehicle results were specifically correlated with particle size and can best be represented by their average uranium mass concentrations of 65

Civilian and military uses of depleted uranium. Environmental and health problems

International Nuclear Information System (INIS)

Cantaluppi, C.; Degetto, S.

2000-01-01

Depleted uranium is a by-product of the process of enrichment of natural uranium and is classified as a toxic and radioactive waste; it has a very high density (approximately 19 g cm - 3), a remarkable ductility and a cost low enough to be attractive for some particular technical applications. Civilian uses are essentially related to its high density, but the prevailing use is however military (production of projectiles). From the radioactive point of view, the exposure to depleted uranium can result from both external irradiation as well as internal contamination. The associated risks are however mainly of chemical-toxicological kind and the target organ is the kidney. In the present note the recent military uses and the possible effects of its environmental diffusion are discussed [it

Kr ion irradiation study of the depleted-uranium alloys

Science.gov (United States)

Gan, J.; Keiser, D. D.; Miller, B. D.; Kirk, M. A.; Rest, J.; Allen, T. R.; Wachs, D. M.

2010-12-01

Fuel development for the reduced enrichment research and test reactor (RERTR) program is tasked with the development of new low enrichment uranium nuclear fuels that can be employed to replace existing high enrichment uranium fuels currently used in some research reactors throughout the world. For dispersion type fuels, radiation stability of the fuel-cladding interaction product has a strong impact on fuel performance. Three depleted-uranium alloys are cast for the radiation stability studies of the fuel-cladding interaction product using Kr ion irradiation to investigate radiation damage from fission products. SEM analysis indicates the presence of the phases of interest: U(Al, Si) 3, (U, Mo)(Al, Si) 3, UMo 2Al 20, U 6Mo 4Al 43 and UAl 4. Irradiations of TEM disc samples were conducted with 500 keV Kr ions at 200 °C to ion doses up to 2.5 × 10 19 ions/m 2 (˜10 dpa) with an Kr ion flux of 10 16 ions/m 2/s (˜4.0 × 10 -3 dpa/s). Microstructural evolution of the phases relevant to fuel-cladding interaction products was investigated using transmission electron microscopy.

Health surveillance of personnel engaged in decontamination of depleted uranium contaminated regions

Energy Technology Data Exchange (ETDEWEB)

Djurovic, B. [Military Medical Academy, Radiological Protection Dept., Belgrade, Serbia and Montenegro (Yugoslavia); Spasic-Jokic, V. [ESLA Accelerator Installation, Lab. of Physics, VINCA Institute of Nuclear Sciences, Belgrade, Serbia and Montenegro (Yugoslavia); Fortuna, D.; Milenkovic, M. [NBH Military Educational Center, Krusevac, Serbia and Montenegro (Yugoslavia)

2006-07-01

After the NATO actions against Serbia and Montenegro, 112 locations were highly contaminated with depleted uranium-112 locations in Kosovo, 7 in the south of Serbia and 1 in Montenegro. Contaminated regions were marked, isolated and some of them decontaminated. In this paper we present the health surveillance protocol created for personnel engaged in decontamination of contaminated regions of Pljackovica and Bratoselce. They were examined and selected before decontamination and only healthy professionals (36 and 28) were engaged. Examination included: general clinical assessment, complete blood count with differential white blood cells; biochemical analysis of blood and urine, specifically renal and liver functions tests, cytogenetic tests (chromosomal aberration and micronucleus test), and laser fluorometry of 24-h urine sample and gamma spectrometry of the same if the levels were elevated. After the decontamination in the first group no clinical or biochemical changes were found, but in 3 of 36 were found unstable chromosomal aberrations. In the second group, in 3 of 28 were found unstable chromosomal aberrations and in 3 of them laser fluorometry analysis showed elevated levels of uranium (>3 {mu}g/l in two, and >5 {mu}g/l in one of them). Gamma spectrometry showed that it was not depleted, but naturally occurring uranium. Additionally performed analysis showed they were from the same village which is in the zone of highly elevated uranium level in ground and water. Three months later no chromosomal changes were found. (authors)

Evaluating the effectiveness of dilution of the recovered uranium with depleted uranium and low-enriched uranium to obtain fuel for VVER reactors

International Nuclear Information System (INIS)

Smirnov, A Yu; Sulaberidze, G A; Dudnikov, A A; Nevinitsa, V A

2016-01-01

The possibility of the recovered uranium enrichment in a cascade of gas centrifuges with three feed flows (depleted uranium, low-enriched uranium, recovered uranium) with simultaneous dilution of U-232,234,236 isotopes was shown. A series of numerical experiments were performed for different content of U-235 in low-enriched uranium. It has been demonstrated that the selected combination of diluents can simultaneously reduce the cost of separative work and the consumption of natural uranium, not only with respect to the previously used multi-flow cascade schemes, but also in comparison to the standard cascade for uranium enrichment. (paper)

Depleted uranium internal contamination of US soldiers deployed in Samawah, Iraq during operation Iraqi freedom

International Nuclear Information System (INIS)

Asaf Durakovic; Isaac Zimmerman; Axel Gerdes

2004-01-01

Purpose: The purpose of this study was to analyze the concentration and precise isotopic composition and ratios of four uranium isotopes ( 234 U, 235 U, 236 U, and 238 U) in the urine of United States soldiers deployed in Samawah, Iraq during the second Gulf War. Methods: Seven active duty US soldiers deployed as military police unit 442 presenting with non-specific symptoms of intractable headaches, excessive fatigue, intermittent fevers, musculoskeletal pains, respiratory impairment, affect changes, urinary tract symptoms, and neurological alterations were clinically evaluated. Each soldier signed a consent form to participate in our study. The collection of 24-hour urine samples of each subject was performed under controlled conditions. The urine samples were personally carried to the laboratory of the Institute of Geochemistry, JW Goethe University, Frankfurt, Germany. Each sample was analyzed in duplicate by multicollector inductively coupled plasma ionization mass spectrometry (MC-ICP-MS). Control samples consisting of an internal urine standard were also analyzed by the same procedure. The analytical methodology included pre-concentration of the urine samples using evaporation, oxidation of organic matter, uranium purification by ion-exchange chromatography, and analysis by mass spectrometry. The final analysis of the specimens was performed by using a double-focusing Thermo Finnigan Neptune multicollector ICP-MS equipped with retarding potential quadrupole lens and a secondary electron multiplier for ion counting. Results: The mean concentration of total uranium was 3.6±1.3 ng/L. The average 238 U/ 235 U ratio was 146.2±10.2. The ratio of 238 U/ 235 U, being considered as the single most important parameter in determining the quantitative state of depletion of the natural uranium ratio, demonstrates a significant internal contamination with depleted uranium in four soldiers. The 234 U/ 238 U ratio was 6.5 x 10 -5 ±5.7 x 10 -6 . The 236 U/ 238 U ratio was

Acid Dissolution of Depleted Uranium from Catalyst using Microwave

Energy Technology Data Exchange (ETDEWEB)

Sung, Jin Hyun; Jeong, Seong Gi; Park, Kwang Heon [Kyunghee University, Yongin (Korea, Republic of)

2011-05-15

The separation process of uranium is one of the most important fields in nuclear industry because uranium is used primary in nuclear power plants. Uranium ores are treated by either acid or alkaline reagents. Uranium can be dissolved by acid or alkaline solutions. There are two oxidation states in which the hexavalent form, the oxide of which is UO{sub 3}, and the tetravalent form, the oxide of which is UO{sub 2}. However, depleted uranium(DU) has also been used as a catalyst in specialized chemical reaction such as ammoxidation. The preferred catalyst for propylene oxidation with ammonia was a uranium oxide-antimony oxide composition. The active phase of catalyst was known as USbO{sub 5} and USb{sub 3}O{sub 10}. There is pentavalent form. Waste catalyst containing DU was generated and stored in chemical industry. In this work, we removed DU from catalyst by acid dissolution

Teratogenicity of depleted uranium aerosols: A review from an epidemiological perspective

Directory of Open Access Journals (Sweden)

Panikkar Bindu

2005-08-01

Full Text Available Abstract Background Depleted uranium is being used increasingly often as a component of munitions in military conflicts. Military personnel, civilians and the DU munitions producers are being exposed to the DU aerosols that are generated. Methods We reviewed toxicological data on both natural and depleted uranium. We included peer reviewed studies and gray literature on birth malformations due to natural and depleted uranium. Our approach was to assess the "weight of evidence" with respect to teratogenicity of depleted uranium. Results Animal studies firmly support the possibility that DU is a teratogen. While the detailed pathways by which environmental DU can be internalized and reach reproductive cells are not yet fully elucidated, again, the evidence supports plausibility. To date, human epidemiological data include case examples, disease registry records, a case-control study and prospective longitudinal studies. Discussion The two most significant challenges to establishing a causal pathway between (human parental DU exposure and the birth of offspring with defects are: i distinguishing the role of DU from that of exposure to other potential teratogens; ii documentation on the individual level of extent of parental DU exposure. Studies that use biomarkers, none yet reported, can help address the latter challenge. Thoughtful triangulation of the results of multiple studies (epidemiological and other of DU teratogenicity contributes to disentangling the roles of various potentially teratogenic parental exposures. This paper is just such an endeavor. Conclusion In aggregate the human epidemiological evidence is consistent with increased risk of birth defects in offspring of persons exposed to DU.

Depleted uranium in the environment - an issue of concern?

International Nuclear Information System (INIS)

Stegnar, P.; Benedik, Lj.

2002-01-01

Natural uranium (U) occurs in soils in typical concentrations of a few parts per milion. U-238 is the most abundant isotope in natural uranium (fraction by weight in natural uranium is 99.28%) and decays into other radioactive elements. A radioactive waste product of uranium enrichment is known as 'depleted uranium' (DU) which is basically natural uranium in which the fissionable U-235 isotopic content has been reduced from 0.71% to 0.2-0.3%. It is practically pure alpha emitter, only selected (in=growth) daughter products are gammaand beta emitters. Comparison of radioactivity shows that the total activity in 1mg of natural uranium is 25.28 Bq and in1 mg of DU is 14.80 Bq. The radioactivity of DU is 60% of that of natural uranium. Currently in the USA alone, there are about 600.000 tonnes of DU in storage. DU is cheap and it is available in large quantities. It is widely used as ballast or counterbalances in ships and aircrafts, as radiation shielding and in non-nuclear civil applications requiring hugh density material. (author)

Depleted uranium oxides as spent-nuclear-fuel waste-package fill materials

International Nuclear Information System (INIS)

Forsberg, C.W.

1997-01-01

Depleted uranium dioxide fill inside the waste package creates the potential for significant improvements in package performance based on uranium geochemistry, reduces the potential for criticality in a repository, and consumes DU inventory. As a new concept, significant uncertainties exist: fill properties, impacts on package design, post- closure performance

Is depleted uranium a threat to health and the environment?

International Nuclear Information System (INIS)

2002-01-01

This issue has come to the fore in recent years now that Norwegian military personnel have been sent to regions of the world where ammunition made of depleted uranium has been used. A number of surveys have been conducted in the Balkans, so far indicating no health hazards to people present in these areas. However, the latest international surveys show that contamination may be long-lasting. Tonje Sekse represented the Norwegian Radiation Protection Authority at the United Nations Environment Programme's (UNEP) inspection tour to Serbia and Montenegro in the autumn of 2001. The report, entitled ''Depleted uranium in Serbia and Montenegro - Post-Conflict Environmental Assessment in the Federal Republic of Yugoslavia'' was published by UNEP in March 2002.(author)

Search for the truth about the NATO use of depleted uranium in the war against Yugoslavia - truth under the DU carpet

International Nuclear Information System (INIS)

Ajdacic, V.; Jaksic, P.

2002-01-01

Having produced thousands atomic, hydrogen and neutron bombs USA and other members of NATO possess large amount of nuclear waste, which also includes depleted uranium. Depleted uranium is natural uranium out of which 0.5% of Uranium-235 isotope is removed to be used for atomic bombs and nuclear fuel. Produced in this way, 'depleted uranium' is still highly radioactive. In one kilogram of such uranium 25 million radioactive decays take place in one second. During the NATO war against Yugoslavia in 1999 their planes A-10 fired the shells containing 272 grams of depleted uranium as they did previously in the Gulf war with Iraq and in 1995 against the Serbs in former Bosnia and Herzegovina. The effects of this 'dirty weapon', forbidden by international conventions, have been already known as disastrous, causing not only human but ecological consequences as well. That is why depleted uranium got the name: metal of dishonor. After long denial, on May the 3 rd American General Chuck Weld has confessed that NATO aviation is using ammunition with depleted uranium in the war against Yugoslavia in Kosovo and Metohija. Number of the locations under the fire of depleted uranium after the war was rising with time. At the beginning NATO information contained small number of such 'targets', 20-30. When the soldiers of the UN peacekeeping forces at Kosovo became ill, NATO was forced to reveal the new data of the used depleted uranium. In their report from January 24, 2001 (Updated on February 8 same year) they claim that 112 locations in Kosovo and Montenegro were exposed to depleted uranium rounds fired from the guns GAU-8 of A-10 planes. According to this report one can estimate the use of about 9 tons of depleted uranium. Our careful analysis points to many mistakes, lack of data, misleading conclusions and contradictions. At least 115 locations were contaminated by depleted uranium. The minimal number of rounds could be close to 43,300, e.g. minimum 12 tons of depleted uranium

Estimation of terrorist attack resistibility of dual-purpose cask TP-117 with DU (depleted uranium) gamma shield

International Nuclear Information System (INIS)

Alekseev, O.G.; Matveev, V.Z.; Morenko, A.I.; Il'kaev, R.I.; Shapovalov, V.I.

2004-01-01

Report is devoted to numerical research of dual-purpose unified cask (used for SFA transportation and storage) resistance to terrorist attacks. High resistance of dual-purpose unified cask has been achieved due to the unique design-technological solutions and implementation of depleted uranium in cask construction. In suggested variant of construction depleted uranium fulfils functions of shielding and constructional material. It is used both in metallic and cermet form (basing on steel and depleted uranium dioxide). Implementation of depleted uranium in cask construction allows maximal load in existing overall dimensions of the cask. At the same time: 1) all safety requirements (IAEA) are met, 2) dual-purpose cask with SFA has high resistance to terrorist attacks

Estimation of terrorist attack resistibility of dual-purpose cask TP-117 with DU (depleted uranium) gamma shield

Energy Technology Data Exchange (ETDEWEB)

Alekseev, O.G.; Matveev, V.Z.; Morenko, A.I.; Il' kaev, R.I.; Shapovalov, V.I. [Russian Federal Nuclear Center - All-Russian Research Inst. of Experimental Physics, Sarov (Russian Federation)

2004-07-01

Report is devoted to numerical research of dual-purpose unified cask (used for SFA transportation and storage) resistance to terrorist attacks. High resistance of dual-purpose unified cask has been achieved due to the unique design-technological solutions and implementation of depleted uranium in cask construction. In suggested variant of construction depleted uranium fulfils functions of shielding and constructional material. It is used both in metallic and cermet form (basing on steel and depleted uranium dioxide). Implementation of depleted uranium in cask construction allows maximal load in existing overall dimensions of the cask. At the same time: 1) all safety requirements (IAEA) are met, 2) dual-purpose cask with SFA has high resistance to terrorist attacks.

The corrosion of depleted uranium in terrestrial and marine environments

International Nuclear Information System (INIS)

Toque, C.; Milodowski, A.E.; Baker, A.C.

2014-01-01

Depleted Uranium alloyed with titanium is used in armour penetrating munitions that have been fired in a number of conflict zones and testing ranges including the UK ranges at Kirkcudbright and Eskmeals. The study presented here evaluates the corrosion of DU alloy cylinders in soil on these two UK ranges and in the adjacent marine environment of the Solway Firth. The estimated mean initial corrosion rates and times for complete corrosion range from 0.13 to 1.9 g cm −2 y −1 and 2.5–48 years respectively depending on the particular physical and geochemical environment. The marine environment at the experimental site was very turbulent. This may have caused the scouring of corrosion products and given rise to a different geochemical environment from that which could be easily duplicated in laboratory experiments. The rate of mass loss was found to vary through time in one soil environment and this is hypothesised to be due to pitting increasing the surface area, followed by a build up of corrosion products inhibiting further corrosion. This indicates that early time measurements of mass loss or corrosion rate may be poor indicators of late time corrosion behaviour, potentially giving rise to incorrect estimates of time to complete corrosion. The DU alloy placed in apparently the same geochemical environment, for the same period of time, can experience very different amounts of corrosion and mass loss, indicating that even small variations in the corrosion environment can have a significant effect. These effects are more significant than other experimental errors and variations in initial surface area. -- Highlights: ► In-situ experiments were conducted to evaluate corrosion rates of depleted uranium. ► Samples were corroded in marine sediments, open sea water and two terrestrial soils. ► The depleted uranium titanium alloy corroded fastest in the marine environments. ► Rates of mass loss can vary through time if corrosion products are not removed. �

Uranium: myths and realities the depleted uranium; Uranio: Mitos y realidades. El caso del uranio emprobrecido

Energy Technology Data Exchange (ETDEWEB)

Sanchez, G.

2001-07-01

Uranium is an element whose name causes worry. The uranium properties are very unknown for people. However the element plays an important roll in the Earth as responsible of numerous natural phenomena, which are vital for life evolution. An example of the low knowledge about uranium has been the Balkan syndrome. A relation between cancers and the use of depleted uranium in ammunition in the Balkan War has been pretended to be established. From the beginning, this hypothesis could have been discarded as it has been confirmed and stated in recent reports of UNEP Commissions who have studied this matter. (Author)

Estimates of radiological risk from depleted uranium weapons in war scenarios.

Science.gov (United States)

Durante, Marco; Pugliese, Mariagabriella

2002-01-01

Several weapons used during the recent conflict in Yugoslavia contain depleted uranium, including missiles and armor-piercing incendiary rounds. Health concern is related to the use of these weapons, because of the heavy-metal toxicity and radioactivity of uranium. Although chemical toxicity is considered the more important source of health risk related to uranium, radiation exposure has been allegedly related to cancers among veterans of the Balkan conflict, and uranium munitions are a possible source of contamination in the environment. Actual measurements of radioactive contamination are needed to assess the risk. In this paper, a computer simulation is proposed to estimate radiological risk related to different exposure scenarios. Dose caused by inhalation of radioactive aerosols and ground contamination induced by Tomahawk missile impact are simulated using a Gaussian plume model (HOTSPOT code). Environmental contamination and committed dose to the population resident in contaminated areas are predicted by a food-web model (RESRAD code). Small values of committed effective dose equivalent appear to be associated with missile impacts (50-y CEDE radiological risk. These computer simulations suggest that little radiological risk is associated to the use of depleted uranium weapons.

Spall wave-profile and shock-recovery experiments on depleted uranium

International Nuclear Information System (INIS)

Hixson, R.S.; Vorthman, J.E.; Gustavsen, R.L.; Zurek, A.K.; Thissell, W.R.; Tonks, D.L.

1998-01-01

Depleted Uranium of two different purity levels has been studied to determine spall strength under shock wave loading. A high purity material with approximately 30 ppm of carbon impurities was shock compressed to two different stress levels, 37 and 53 kbar. The second material studied was uranium with about 300 ppm of carbon impurities. This material was shock loaded to three different final stress level, 37, 53, and 81 kbar. Two experimental techniques were used in this work. First, time-resolved free surface particle velocity measurements were done using a VISAR velocity interferometer. The second experimental technique used was soft recovery of samples after shock loading. These two experimental techniques will be briefly described here and VISAR results will be shown. Results of the spall recovery experiments and subsequent metallurgical analyses are described in another paper in these proceedings. copyright 1998 American Institute of Physics

Transpassive electrodissolution of depleted uranium in alkaline electrolytes

International Nuclear Information System (INIS)

Weisbrod, K.R.; Schake, A.R.; Morgan, A.N.; Purdy, G.M.; Martinez, H.E.; Nelson, T.O.

1998-03-01

To aid in removal of oralloy from the nuclear weapons stockpile, scientists at the Los Alamos National Laboratory Plutonium Facility are decontaminating oralloy parts by electrodissolution in neutral to alkaline electrolytes composed of sodium nitrate and sodium sulfate. To improve the process, electrodissolution experiments were performed with depleted uranium to understand the effects of various operating parameters. Sufficient precipitate was also produced to evaluate the feasibility of using ultrafiltration to separate the uranium oxide precipitates from the electrolyte before it enters the decontamination fixture. In preparation for the experiments, a potential-pH diagram for uranium was constructed from thermodynamic data for fully hydrated species. Electrodissolution in unstirred solutions showed that uranium dissolution forms two layers, an acidic bottom layer rich in uranium and an alkaline upper layer. Under stirred conditions results are consistent with the formation of a yellow precipitate of composition UO 3 ·2H 2 O, a six electron process. Amperometric experiments showed that current efficiency remained near 100% over a wide range of electrolytes, electrolyte concentrations, pH, and stirring conditions

A model for beta skin dose estimation due to the use of a necklace with uranium depleted bullets

International Nuclear Information System (INIS)

Lavalle Heibron, P.H.; Pérez Guerrero, J.S.; Oliveira, J.F. de

2015-01-01

Depleted uranium bullets were use as munitions during the Kuwait – Iraq war and the International Atomic Energy Agency sampling expert’s team found fragments in the environment when the war was over. Consequently, there is a possibility that members of the public, especially children, collects DU fragments and use it, for example, to make a necklace. This paper estimates the beta skin dose to a child that uses a necklace made with a depleted uranium bullet. The theoretical model for dose estimation is based on Loevinguer’s equation with a correction factor adjusted for the maximum beta energy in the range between 0.1 and 2.5 MeV calculated taking into account the International Atomic Energy Agency expected doses rates in air at one meter distance of a point source of 37 GBq, function of the maximum beta energy. The dose rate estimated by this work due to the child use of a necklace with one depleted uranium bullet of 300 g was in good agreement with other results founded in literature. (authors)

Kr ion irradiation study of the depleted-uranium alloys

Energy Technology Data Exchange (ETDEWEB)

Gan, J., E-mail: Jian.Gan@inl.go [Idaho National Laboratory, P.O. Box 1625, Idaho Falls, ID 83415-6188 (United States); Keiser, D.D. [Idaho National Laboratory, P.O. Box 1625, Idaho Falls, ID 83415-6188 (United States); Miller, B.D. [University of Wisconsin, 1500 Engineering Drive, Madison, WI 53706 (United States); Kirk, M.A.; Rest, J. [Argonne National Laboratory, 9700 South Cass Ave., Argonne, IL 60439 (United States); Allen, T.R. [University of Wisconsin, 1500 Engineering Drive, Madison, WI 53706 (United States); Wachs, D.M. [Idaho National Laboratory, P.O. Box 1625, Idaho Falls, ID 83415-6188 (United States)

2010-12-01

Fuel development for the reduced enrichment research and test reactor (RERTR) program is tasked with the development of new low enrichment uranium nuclear fuels that can be employed to replace existing high enrichment uranium fuels currently used in some research reactors throughout the world. For dispersion type fuels, radiation stability of the fuel-cladding interaction product has a strong impact on fuel performance. Three depleted-uranium alloys are cast for the radiation stability studies of the fuel-cladding interaction product using Kr ion irradiation to investigate radiation damage from fission products. SEM analysis indicates the presence of the phases of interest: U(Al, Si){sub 3}, (U, Mo)(Al, Si){sub 3}, UMo{sub 2}Al{sub 20}, U{sub 6}Mo{sub 4}Al{sub 43} and UAl{sub 4}. Irradiations of TEM disc samples were conducted with 500 keV Kr ions at 200 {sup o}C to ion doses up to 2.5 x 10{sup 19} ions/m{sup 2} ({approx}10 dpa) with an Kr ion flux of 10{sup 16} ions/m{sup 2}/s ({approx}4.0 x 10{sup -3} dpa/s). Microstructural evolution of the phases relevant to fuel-cladding interaction products was investigated using transmission electron microscopy.

Enriched but not depleted uranium affects central nervous system in long-term exposed rat.

Science.gov (United States)

Houpert, Pascale; Lestaevel, Philippe; Bussy, Cyrill; Paquet, François; Gourmelon, Patrick

2005-12-01

Uranium is well known to induce chemical toxicity in kidneys, but several other target organs, such as central nervous system, could be also affected. Thus in the present study, the effects on sleep-wake cycle and behavior were studied after chronic oral exposure to enriched or depleted uranium. Rats exposed to 4% enriched uranium for 1.5 months through drinking water, accumulated twice as much uranium in some key areas such as the hippocampus, hypothalamus and adrenals than did control rats. This accumulation was correlated with an increase of about 38% of the amount of paradoxical sleep, a reduction of their spatial working memory capacities and an increase in their anxiety. Exposure to depleted uranium for 1.5 months did not induce these effects, suggesting that the radiological activity induces the primary events of these effects of uranium.

Measuring aerosols generated inside armoured vehicles perforated by depleted uranium ammunition

International Nuclear Information System (INIS)

Parkhurst, M.A.

2003-01-01

In response to questions raised after the Gulf War about the health significance of exposure to depleted uranium (DU), the US Department of Defense initiated a study designed to provide an improved scientific basis for assessment of possible health effects on soldiers in vehicles struck by these munitions. As part of this study, a series of DU penetrators were fired at an Abrams tank and a Bradley fighting vehicle, and the aerosols generated by vehicle perforation were collected and characterised. A robust sampling system was designed to collect aerosols in this difficult environment and monitor continuously the sampler flow rates. The aerosol samplers selected for these tests included filter cassettes, cascade impactors, a five-stage cyclone and a moving filter. Sampler redundancy was an integral part of the sampling system to offset losses from fragment damage. Wipe surveys and deposition trays collected removable deposited particulate matter. Interior aerosols were analysed for uranium concentration and particle size distribution as a function of time. They were also analysed for uranium oxide phases, particle morphology and dissolution in vitro. These data, currently under independent peer review, will provide input for future prospective and retrospective dose and health risk assessments of inhaled or ingested DU aerosols. This paper briefly discusses the target vehicles, firing trajectories, aerosol samplers and instrumentation control systems, and the types of analyses conducted on the samples. (author)

Gamma-ray line intensities for depleted uranium

International Nuclear Information System (INIS)

Moss, C.E.

1985-01-01

Measurements of the gamma-ray line intensities from depleted uranium allowed us to determine which of two conflicting previous experiments was correct. For the 1001-keV line we obtain a branching ratio of 0.834 +- 0.007, in good agreement with one of the previous experiments. A table compares our intensities for several lines with those obtained in previous experiments. 5 refs., 2 figs., 1 tab

Determination of average fission fraction produced by 14 MeV neutrons in assemblies with large volume of depleted uranium

International Nuclear Information System (INIS)

Wang Dalun; Li Benci; Wang Xiuchun; Li Yijun; Zhang Shaohua; He Yongwu

1991-07-01

The average fission fraction of 238 U caused by 14 MeV neutrons in assemblies with large volume depleted uranium has been determined. The measured value of p f 238U (R ∞ depleted ) 14 was 0.897 ± 0.036. Measurements were also completed for neutron flux distribution and average fission fraction of 235 U isotope in depleted uranium sphere. Values of p f 238U (R depleted ) have been obtained by using a series of uranium spheres. For a sphere with Φ 600 the p f 23 '8 U (R 300 depleted ) is 0.823 ± 0.041, the density of depleted uranium assembly is 18.8g/cm 3 and total weight of assembly is about 2.8t

Depleted uranium residual radiological risk assessment for Kosovo sites

International Nuclear Information System (INIS)

Durante, Marco; Pugliese, Mariagabriella

2003-01-01

During the recent conflict in Yugoslavia, depleted uranium rounds were employed and were left in the battlefield. Health concern is related to the risk arising from contamination of areas in Kosovo with depleted uranium penetrators and dust. Although chemical toxicity is the most significant health risk related to uranium, radiation exposure has been allegedly related to cancers among veterans of the Balkan conflict. Uranium munitions are considered to be a source of radiological contamination of the environment. Based on measurements and estimates from the recent Balkan Task Force UNEP mission in Kosovo, we have estimated effective doses to resident populations using a well-established food-web mathematical model (RESRAD code). The UNEP mission did not find any evidence of widespread contamination in Kosovo. Rather than the actual measurements, we elected to use a desk assessment scenario (Reference Case) proposed by the UNEP group as the source term for computer simulations. Specific applications to two Kosovo sites (Planeja village and Vranovac hill) are described. Results of the simulations suggest that radiation doses from water-independent pathways are negligible (annual doses below 30 μSv). A small radiological risk is expected from contamination of the groundwater in conditions of effective leaching and low distribution coefficient of uranium metal. Under the assumptions of the Reference Case, significant radiological doses (>1 mSv/year) might be achieved after many years from the conflict through water-dependent pathways. Even in this worst-case scenario, DU radiological risk would be far overshadowed by its chemical toxicity

Summary of the Preliminary Analysis of Savannah River Depleted Uranium Trioxide

International Nuclear Information System (INIS)

2010-01-01

This report summarizes a preliminary special analysis of the Savannah River Depleted Uranium Trioxide waste stream (SVRSURANIUM03, Revision 2). The analysis is considered preliminary because a final waste profile has not been submitted for review. The special analysis is performed to determine the acceptability of the waste stream for shallow land burial at the Area 5 Radioactive Waste Management Site (RWMS) at the Nevada National Security Site (NNSS). The Savannah River Depleted Uranium Trioxide waste stream requires a special analysis because the waste stream's sum of fractions exceeds one. The 99Tc activity concentration is 98 percent of the NNSS Waste Acceptance Criteria and the largest single contributor to the sum of fractions.

10 CFR 34.67 - Records of leak testing of sealed sources and devices containing depleted uranium.

Science.gov (United States)

2010-01-01

... 10 Energy 1 2010-01-01 2010-01-01 false Records of leak testing of sealed sources and devices containing depleted uranium. 34.67 Section 34.67 Energy NUCLEAR REGULATORY COMMISSION LICENSES FOR INDUSTRIAL... Requirements § 34.67 Records of leak testing of sealed sources and devices containing depleted uranium. Each...

Radiation survey and decontamination of cape Arza from depleted uranium

Directory of Open Access Journals (Sweden)

Vukotić Perko

2003-01-01

Full Text Available In the action of NATO A-10 airplanes in 1999, the cape Arza, Serbia and Montenegro was contaminated by depleted uranium. The clean-up operations were undertaken at the site, and 242 uranium projectiles and their 49 larger fragments were removed from the cape. That is about 85% of the total number of projectiles by which Arza was contaminated. Here are described details of the applied procedures and results of the soil radioactivity measurements after decontamination.

Gulf war depleted uranium risks.

Science.gov (United States)

Marshall, Albert C

2008-01-01

US and British forces used depleted uranium (DU) in armor-piercing rounds to disable enemy tanks during the Gulf and Balkan Wars. Uranium particulate is generated by DU shell impact and particulate entrained in air may be inhaled or ingested by troops and nearby civilian populations. As uranium is slightly radioactive and chemically toxic, a number of critics have asserted that DU exposure has resulted in a variety of adverse health effects for exposed veterans and nearby civilian populations. The study described in this paper used mathematical modeling to estimate health risks from exposure to DU during the 1991 Gulf War for both US troops and nearby Iraqi civilians. The analysis found that the risks of DU-induced leukemia or birth defects are far too small to result in an observable increase in these health effects among exposed veterans or Iraqi civilians. The analysis indicated that only a few ( approximately 5) US veterans in vehicles accidentally targeted by US tanks received significant exposure levels, resulting in about a 1.4% lifetime risk of DU radiation-induced fatal cancer (compared with about a 24% risk of a fatal cancer from all other causes). These veterans may have also experienced temporary kidney damage. Iraqi children playing for 500 h in DU-destroyed vehicles are predicted to incur a cancer risk of about 0.4%. In vitro and animal tests suggest the possibility of chemically induced health effects from DU internalization, such as immune system impairment. Further study is needed to determine the applicability of these findings for Gulf War exposure to DU. Veterans and civilians who did not occupy DU-contaminated vehicles are unlikely to have internalized quantities of DU significantly in excess of normal internalization of natural uranium from the environment.

Depleted-Uranium Weapons: the Whys and Wherefores

OpenAIRE

Gsponer, Andre

2003-01-01

The only military application in which depleted-uranium (DU) alloys out-perform present-day tungsten alloys is long-rod penetration into a main battle-tank's armor. However, this advantage is only on the order of 10%, and it disappears when the comparison is made in terms of actual lethality of complete anti-tank systems instead of laboratory-type steel penetration capability. Therefore, new micro- and nano-engineered tungsten alloys may soon out-perform DU alloys, enabling the production of ...

Depleted uranium hexafluoride management program : data compilation for the K-25 site

International Nuclear Information System (INIS)

Hartmann, H. M.

2001-01-01

This report is a compilation of data and analyses for the K-25 site on the Oak Ridge Reservation, Oak Ridge, Tennessee. The data were collected and the analyses were done in support of the U.S. Department of Energy (DOE) 1999 Programmatic Environmental Impact Statement for Alternative Strategies for the Long-Term Management and Use of Depleted Uranium Hexafluoride (DOE/EIS-0269). The report describes the affected environment at the K-25 site and summarizes the potential environmental impacts that could result from continued cylinder storage and preparation of cylinders for shipment at the site. It is probable that the cylinders at the K-25 site will be shipped to another site for conversion. Because conversion and long-term storage of the entire inventory at the K-25 site are highly unlikely, these data are not presented in this report. DOE's preferred alternative is to begin converting the depleted uranium hexafluoride inventory as soon as possible to either uranium oxide, uranium metal, or a combination of both, while allowing for use of as much of this inventory as possible

Characterization of uranium isotopic abundances in depleted uranium metal assay standard 115

International Nuclear Information System (INIS)

Mathew, K.J.; Singleton, G.L.; Essex, R.M.; Hasozbek, A.; Orlowicz, G.; Soriano, M.

2013-01-01

Certified reference material (CRM) 115, Uranium (Depleted) Metal (Uranium Assay Standard), was analyzed using a TRITON Thermal Ionization Mass Spectrometer to characterize the uranium isotope-amount ratios. The certified 235 U/ 238 U 'major' isotope-amount ratio of 0.0020337 (12) in CRM 115 was determined using the total evaporation (TE) and the modified total evaporation (MTE) analytical techniques. In the MTE method, the total evaporation process is interrupted on a regular basis to allow correction of background from peak tailing, internal calibration of the secondary electron multiplier detector versus the Faraday cups, peak-centering, and ion source re-focusing. For the 'minor' 234 U/ 238 U and 236 U/ 238 U isotope-amount ratio measurements using MTE, precision and accuracy comparable to conventional analyses are achieved, without compromising the quality of the 235 U/ 238 U isotope-amount ratios. Characterized values of the 234 U/ 238 U and 236 U/ 238 U isotope-amount ratios in CRM 115 are 0.000007545 (10) and 0.000032213 (84), respectively. The 233 U/ 238 U isotope-amount ratio in CRM 115 is estimated to be -9 . The homogeneity of the CRM 115 materials is established through the absence of any statistically significant unit-to-unit variation in the uranium isotope-amount ratios. The measurements leading to the certification of uranium isotope-amount ratios are discussed. (author)

Review of the toxicologic and radiologic risks to military personnel from exposure to depleted uranium during and after combat

National Research Council Canada - National Science Library

National Academies Press (U.S.); National Research Council (U.S.). Board on Environmental Studies and Toxicology; National Research Council (U.S.) Committee on Toxicologic and Radiologic Effects from Exposure to Depleted Uranium During and After Combat

2008-01-01

.... Depleted uranium is a toxic heavy metal and is weakly radioactive. Concerns have been raised about the adverse health effects from exposure to depleted uranium that is aerosolized during combat...

Overview of toxicity data and risk assessment methods for evaluating the chemical effects of depleted uranium compounds

International Nuclear Information System (INIS)

Hartmann, H.M.; Monette, F.A.; Avci, H.I.

2000-01-01

In the United States, depleted uranium is handled or used in several chemical forms by both governmental agencies and private industry (primarily companies producing and machining depleted uranium metal for military applications). Human exposure can occur as a result of handling these compounds, routine low-level effluent releases to the environment from processing facilities, or materials being accidentally released from storage locations or during processing or transportation. Exposure to uranium can result in both chemical and radiological toxicity, but in most instances chemical toxicity is of greater concern. This article discusses the chemical toxic effects from human exposure to depleted uranium compounds that are likely to be handled during the long-term management and use of depleted uranium hexafluoride (UF 6 ) inventories in the United States. It also reviews representative publications in the toxicological literature to establish appropriate reference values for risk assessments. Methods are described for evaluating chemical toxicity caused by chronic low-level exposure and acute exposure. Example risk evaluations are provided for illustration. Preliminary results indicate that chemical effects of chronic exposure to uranium compounds under normal operating conditions would be negligibly small. Results also show that acute exposures under certain accident conditions could cause adverse chemical effects among the populations exposed.

Energies and media nr 28. Uranium mining exploitations and residues. Uranium mines in Niger. Depleted uranium as a by-product of enrichment

International Nuclear Information System (INIS)

2009-02-01

After some comments on recent events in the nuclear sector in different countries (USA, China, India, UK, Sweden, Italy and France), this publication addresses the issue of uranium mining exploitations and of their residues. It comments the radioactivity in mining areas, briefly discusses the issue of low doses, describes the uranium ore and its processing, indicates which are the various residues of the mining activity (sterile uncovered tailings, non exploitable mineralized rocks, ore and residue processing, residue radioactivity, mine closing down, witnesses on health in ancient mines). Some reflections are stated about uranium mines in Niger, and about depleted uranium as a by-product of the enrichment activity

Depleted uranium concrete container feasibility study

International Nuclear Information System (INIS)

Haelsig, R.T.

1994-09-01

The purpose of this report is to consider the feasibility of using containers constructed of depleted uranium aggregate concrete (DUCRETE) to store and transport radioactive materials. The method for this study was to review the advantages and disadvantages of DUCRETE containers considering design requirements for potential applications. The author found that DUCRETE is a promising material for onsite storage containers, provided DUCRETE vessels can be certified for one-way transport to disposal sites. The author also found that DUCRETE multipurpose spent nuclear fuel storage/transport packages are technically viable, provided altered temperature acceptance limits can be developed for DUCRETE

ZPR-3 Assembly 11: A cylindrical sssembly of highly enriched uranium and depleted uranium with an average 235U enrichment of 12 atom % and a depleted uranium reflector

International Nuclear Information System (INIS)

Lell, R.M.; McKnight, R.D.; Tsiboulia, A.; Rozhikhin, Y.

2010-01-01

Over a period of 30 years, more than a hundred Zero Power Reactor (ZPR) critical assemblies were constructed at Argonne National Laboratory. The ZPR facilities, ZPR-3, ZPR-6, ZPR-9 and ZPPR, were all fast critical assembly facilities. The ZPR critical assemblies were constructed to support fast reactor development, but data from some of these assemblies are also well suited for nuclear data validation and to form the basis for criticality safety benchmarks. A number of the Argonne ZPR/ZPPR critical assemblies have been evaluated as ICSBEP and IRPhEP benchmarks. Of the three classes of ZPR assemblies, engineering mockups, engineering benchmarks and physics benchmarks, the last group tends to be most useful for criticality safety. Because physics benchmarks were designed to test fast reactor physics data and methods, they were as simple as possible in geometry and composition. The principal fissile species was 235 U or 239 Pu. Fuel enrichments ranged from 9% to 95%. Often there were only one or two main core diluent materials, such as aluminum, graphite, iron, sodium or stainless steel. The cores were reflected (and insulated from room return effects) by one or two layers of materials such as depleted uranium, lead or stainless steel. Despite their more complex nature, a small number of assemblies from the other two classes would make useful criticality safety benchmarks because they have features related to criticality safety issues, such as reflection by soil-like material. ZPR-3 Assembly 11 (ZPR-3/11) was designed as a fast reactor physics benchmark experiment with an average core 235 U enrichment of approximately 12 at.% and a depleted uranium reflector. Approximately 79.7% of the total fissions in this assembly occur above 100 keV, approximately 20.3% occur below 100 keV, and essentially none below 0.625 eV - thus the classification as a 'fast' assembly. This assembly is Fast Reactor Benchmark No. 8 in the Cross Section Evaluation Working Group (CSEWG) Benchmark

Depleted uranium (DU) mobility in the natural environment

International Nuclear Information System (INIS)

Ragnarsdottir, K.V.

2002-01-01

In 1999 the Balkan's conflict lead NATO war planes to leave 10x10 3 kg of depleted uranium (DU) in the environment of Kosovo and neighbouring states (UNEP, 2001). DU behaves in the same manner in the environment as natural uranium and it can be traced with isotopic analysis due to the fact that DU has the isotopic composition of 0.2% 235 U and 99.8% 2 38 U as opposed to natural uranium which has 0.7% 2 35 U and 99.3% 2 38 U. DU is a waste product of the nuclear industry which enrich nuclear fuel by 2 35 U. Large stock piles of DU therefore exist in countries that produce nuclear energy and/or nuclear weapons. The DU is given to the weapons industry for free (or cheap) and has been a popular choice for armour penetrating arsenal due to the high density of uranium (19 g cm -3 ) and therefore its high penetrating power. Indeed the arsenal used in Kosovo consisted of DU penetrators that were shot from A-10 aeroplanes. They weigh roughly 300 g and have the shape of a fat 9 cm long pencil. (author)

Summary of the engineering analysis report for the long-term management of depleted uranium hexafluoride

International Nuclear Information System (INIS)

Dubrin, J.W.; Rahm-Crites, L.

1997-09-01

The Department of Energy (DOE) is reviewing ideas for the long-term management and use of its depleted uranium hexafluoride. DOE owns about 560,000 metric tons (over a billion pounds) of depleted uranium hexafluoride. This material is contained in steel cylinders located in storage yards near Paducah, Kentucky; Portsmouth, Ohio; and at the East Tennessee Technology Park (formerly the K-25 Site) in Oak Ridge, Tennessee. On November 10, 1994, DOE announced its new Depleted Uranium Hexafluoride Management Program by issuing a Request for Recommendations and an Advance Notice of Intent in the Federal Register (59 FR 56324 and 56325). The first part of this program consists of engineering, costs and environmental impact studies. Part one will conclude with the selection of a long-term management plan or strategy. Part two will carry out the selected strategy

Summary of the engineering analysis report for the long-term management of depleted uranium hexafluoride

Energy Technology Data Exchange (ETDEWEB)

Dubrin, J.W., Rahm-Crites, L.

1997-09-01

The Department of Energy (DOE) is reviewing ideas for the long-term management and use of its depleted uranium hexafluoride. DOE owns about 560,000 metric tons (over a billion pounds) of depleted uranium hexafluoride. This material is contained in steel cylinders located in storage yards near Paducah, Kentucky; Portsmouth, Ohio; and at the East Tennessee Technology Park (formerly the K-25 Site) in Oak Ridge, Tennessee. On November 10, 1994, DOE announced its new Depleted Uranium Hexafluoride Management Program by issuing a Request for Recommendations and an Advance Notice of Intent in the Federal Register (59 FR 56324 and 56325). The first part of this program consists of engineering, costs and environmental impact studies. Part one will conclude with the selection of a long-term management plan or strategy. Part two will carry out the selected strategy.

DUSCOBS - a depleted-uranium silicate backfill for transport, storage, and disposal of spent nuclear fuel

International Nuclear Information System (INIS)

Forsberg, C.W.; Pope, R.B.; Ashline, R.C.; DeHart, M.D.; Childs, K.W.; Tang, J.S.

1995-01-01

A Depleted Uranium Silicate COntainer Backfill System (DUSCOBS) is proposed that would use small, isotopically-depleted uranium silicate glass beads as a backfill material inside storage, transport, and repository waste packages containing spent nuclear fuel (SNF). The uranium silicate glass beads would fill all void space inside the package including the coolant channels inside SNF assemblies. Based on preliminary analysis, the following benefits have been identified. DUSCOBS improves repository waste package performance by three mechanisms. First, it reduces the radionuclide releases from SNF when water enters the waste package by creating a local uranium silicate saturated groundwater environment that suppresses (1) the dissolution and/or transformation of uranium dioxide fuel pellets and, hence, (2) the release of radionuclides incorporated into the SNF pellets. Second, the potential for long-term nuclear criticality is reduced by isotopic exchange of enriched uranium in SNF with the depleted uranium (DU) in the glass. Third, the backfill reduces radiation interactions between SNF and the local environment (package and local geology) and thus reduces generation of hydrogen, acids, and other chemicals that degrade the waste package system. In addition, the DUSCOBS improves the integrity of the package by acting as a packing material and ensures criticality control for the package during SNF storage and transport. Finally, DUSCOBS provides a potential method to dispose of significant quantities of excess DU from uranium enrichment plants at potential economic savings. DUSCOBS is a new concept. Consequently, the concept has not been optimized or demonstrated in laboratory experiments

Measurements of daily urinary uranium excretion in German peacekeeping personnel and residents of the Kosovo region to assess potential intakes of depleted uranium (DU)

International Nuclear Information System (INIS)

Oeh, U.; Priest, N.D.; Roth, P.; Ragnarsdottir, K.V.; Li, W.B.; Hoellriegl, V.; Thirlwall, M.F.; Michalke, B.; Giussani, A.; Schramel, P.; Paretzke, H.G.

2007-01-01

Following the end of the Kosovo conflict, in June 1999, a study was instigated to evaluate whether there was a cause for concern of health risk from depleted uranium (DU) to German peacekeeping personnel serving in the Balkans. In addition, the investigations were extended to residents of Kosovo and southern Serbia, who lived in areas where DU ammunitions were deployed. In order to assess a possible DU intake, both the urinary uranium excretion of volunteer residents and water samples were collected and analysed using inductively coupled plasma-mass spectrometry (ICP-MS). More than 1300 urine samples from peacekeeping personnel and unexposed controls of different genders and age were analysed to determine uranium excretion parameters. The urine measurements for 113 unexposed subjects revealed a daily uranium excretion rate with a geometric mean of 13.9 ng/d (geometric standard deviation (GSD) = 2.17). The analysis of 1228 urine samples from the peacekeeping personnel resulted in a geometric mean of 12.8 ng/d (GSD = 2.60). It follows that both unexposed controls and peacekeeping personnel excreted similar amounts of uranium. Inter-subject variation in uranium excretion was high and no significant age-specific differences were found. The second part of the study monitored 24 h urine samples provided by selected residents of Kosovo and adjacent regions of Serbia compared to controls from Munich, Germany. Total uranium and isotope ratios were measured in order to determine DU content. 235 U/ 238 U ratios were within ± 0.3% of the natural value, and 236 U/ 238 U was less than 2 x 10 -7 , indicating no significant DU in any of the urine samples provided, despite total uranium excretion being relatively high in some cases. Measurements of ground and tap water samples from regions where DU munitions were deployed did not show any contamination with DU, except in one sample. It is concluded that both peacekeeping personnel and residents serving or living in the Balkans

Development of an environmentally friendly protective coating for the depleted uranium-0.75 wt% titanium alloy

International Nuclear Information System (INIS)

Roeper, Donald F.; Chidambaram, Devicharan; Clayton, Clive R.; Halada, Gary P.; Derek Demaree, J.

2006-01-01

Molybdenum oxide-based conversion coatings have been formed on the surface of the depleted uranium-0.75 wt% titanium alloy using either concentrated nitric acid or fluorides for surface activation prior to coating formation. The acid-activated surface forms a coating that offers corrosion protection after a period of aging, when uranium species have migrated to the surface. X-ray photoelectron spectroscopy (XPS) revealed that the protective coating is primarily a polymolybdate bound to a uranyl ion. Rutherford backscattering spectroscopy (RBS) on the acid-activated coatings also shows uranium dioxide migrating to the surface. The fluoride-activated surface does not form a protective coating and there are no uranium species on the surface as indicated by XPS. The coating on the fluoride-activated samples has been found to contain a mixture of molybdenum oxides of which the main component is molybdenum trioxide and a minor component of an Mo(V) oxide

ZPR-3 Assembly 11 : A cylindrical sssembly of highly enriched uranium and depleted uranium with an average {sup 235}U enrichment of 12 atom % and a depleted uranium reflector.

Energy Technology Data Exchange (ETDEWEB)

Lell, R. M.; McKnight, R. D.; Tsiboulia, A.; Rozhikhin, Y.; National Security; Inst. of Physics and Power Engineering

2010-09-30

Over a period of 30 years, more than a hundred Zero Power Reactor (ZPR) critical assemblies were constructed at Argonne National Laboratory. The ZPR facilities, ZPR-3, ZPR-6, ZPR-9 and ZPPR, were all fast critical assembly facilities. The ZPR critical assemblies were constructed to support fast reactor development, but data from some of these assemblies are also well suited for nuclear data validation and to form the basis for criticality safety benchmarks. A number of the Argonne ZPR/ZPPR critical assemblies have been evaluated as ICSBEP and IRPhEP benchmarks. Of the three classes of ZPR assemblies, engineering mockups, engineering benchmarks and physics benchmarks, the last group tends to be most useful for criticality safety. Because physics benchmarks were designed to test fast reactor physics data and methods, they were as simple as possible in geometry and composition. The principal fissile species was {sup 235}U or {sup 239}Pu. Fuel enrichments ranged from 9% to 95%. Often there were only one or two main core diluent materials, such as aluminum, graphite, iron, sodium or stainless steel. The cores were reflected (and insulated from room return effects) by one or two layers of materials such as depleted uranium, lead or stainless steel. Despite their more complex nature, a small number of assemblies from the other two classes would make useful criticality safety benchmarks because they have features related to criticality safety issues, such as reflection by soil-like material. ZPR-3 Assembly 11 (ZPR-3/11) was designed as a fast reactor physics benchmark experiment with an average core {sup 235}U enrichment of approximately 12 at.% and a depleted uranium reflector. Approximately 79.7% of the total fissions in this assembly occur above 100 keV, approximately 20.3% occur below 100 keV, and essentially none below 0.625 eV - thus the classification as a 'fast' assembly. This assembly is Fast Reactor Benchmark No. 8 in the Cross Section Evaluation

Uranium isotopic analysis of depleted uranium in presence of other radioactive materials by using nondestructive gamma-ray measurements in coaxial and planar Ge detectors

International Nuclear Information System (INIS)

Yucel, H.; Yeltepe, E.; Dikmen, H.; Turhan, Sh.; Vural, M.

2006-01-01

Full text: The isotopic abundance of depleted uranium samples in the presence of other radioactive materials, especially actinide isotopes such as Th 232, Np 237-Pa 233 and Am 241 can be determined from two gamma-ray spectrometric methods. One is the absolute method which employs non-destructive gamma-ray spectrometry for energies below 1001 keV using a coaxial Ge detector calibrated with a set of standards. The other is the multi-group analysis (MGA) method using the low energy region (< 300 keV) with a planar Ge detector intrinsically calibrated with gamma and X-rays of uranium without use of standards. At present absolute method, less intense but cleaner gamma peaks at 163.33 keV (5.08 percent) and 205 keV(5.01 percent) of U 235 are preferred over more intense peaks at 143.76 keV(10.76 percent), possible interference with 143.25 keV(0.44 percent) of Np 237 and 185.705 keV(57.2 percent), possible interference with 186.21 keV(3.51 percent) of Ra 226. In the high energy region the 1001.03 keV(0.837 percent) peak of Pa 234 m is used for the isotopic abundance analysis because the more intense 63.3 keV peak of Th 234 daughter of U 238 parent has a fully multiplet(62.86 keV+63.29 keV) and include the interferences of the 62.70 keV(1.5 percent) peak of Pa 234, the 63.81 keV(0.263 percent) peak of Th 232 and the 63.90 keV(0.011 percent) peak of Np 237. Although the MGA method is quicker and more practical, the more laborious absolute gamma spectrometric method can give more accurate results for the isotopic determination of depleted uranium samples. The relative uranium abundances obtained with the second method (i,e., MGA) are in general inconsistent with the declared values for the uranium samples in the presence of the above mentioned actinides. The reason for these erroneous results is proposed to be the interference of the gamma and X-rays of uranium in the 80-130 keV region used in MGA with those emissions from other radioactive materials present

Influence of hydraulic and geomorphologic components of a semi-arid watershed on depleted-uranium transport

International Nuclear Information System (INIS)

Becker, N.M.

1991-01-01

Investigations were undertaken to determine the fate and transport of depleted uranium away from high explosive firing sites at Los Alamos National Laboratory in north-central New Mexico. Investigations concentrated on a small, semi-arid watershed which drains 5 firing sites. Sampling for uranium in spring/summer/fall runoff, snowmelt runoff, in fallout, and in soil and in sediments revealed that surface water is the main transport mechanism. Although the watershed is less than 8 km 2 , flow discontinuity was observed between the divide and the outlet; flow discontinuity occurs in semi-arid and arid watersheds, but was unexpected at this scale. This region, termed a discharge sink, is an area where all flow infiltrates and all sediment, including uranium, deposits during nearly all flow events; it is estimated that the discharge sink has provided the locale for uranium detention during the last 23 years. Mass balance calculations indicate that over 90% of uranium expended still remains at or nearby the firing sites. Leaching experiments determined that uranium can rapidly dissolve from the solid phase. It is postulated that precipitation and runoff which percolate vertically through uranium-contaminated soil and sediment are capable of transporting uranium in the dissolved phase to deeper strata. This may be the key transport mechanism which moves uranium out of the watershed

Measurements of Radioactive Contamination In Kosovo Battlefields Due to the Use of Depleted Uranium Weapons by NATO Forces

International Nuclear Information System (INIS)

Zucchetti, M.

1999-01-01

During the last war in the Balkan area (Kosovo-Serbia War, spring-summer 1999), NATO forces admitted the use of weapons containing Depleted Uranium. In particular, 30 mm bullets being fired by A-10 anti-tank aircraft and probably all Tomahawk Cruise missiles in this action contain depleted uranium

Hormetic effect induced by depleted uranium in zebrafish embryos

International Nuclear Information System (INIS)

Ng, C.Y.P.; Cheng, S.H.; Yu, K.N.

2016-01-01

Highlights: • Studied hormetic effect induced by uranium (U) in embryos of zebrafish (Danio rerio). • Hormesis observed at 24 hpf for exposures to 10 μg/l of depleted U (DU). • Hormesis not observed before 30 hpf for exposures to 100 μg/l of DU. • Hormetic effect induced in zebrafish embryos in a dose-and time-dependent manner. - Abstract: The present work studied the hormetic effect induced by uranium (U) in embryos of zebrafish (Danio rerio) using apoptosis as the biological endpoint. Hormetic effect is characterized by biphasic dose-response relationships showing a low-dose stimulation and a high-dose inhibition. Embryos were dechorionated at 4 h post fertilization (hpf), and were then exposed to 10 or 100 μg/l depleted uranium (DU) in uranyl acetate solutions from 5 to 6 hpf. For exposures to 10 μg/l DU, the amounts of apoptotic signals in the embryos were significantly increased at 20 hpf but were significantly decreased at 24 hpf, which demonstrated the presence of U-induced hormesis. For exposures to 100 μg/l DU, the amounts of apoptotic signals in the embryos were significantly increased at 20, 24 and 30 hpf. Hormetic effect was not shown but its occurrence between 30 and 48 hpf could not be ruled out. In conclusion, hormetic effect could be induced in zebrafish embryos in a concentration- and time-dependent manner.

Hormetic effect induced by depleted uranium in zebrafish embryos

Energy Technology Data Exchange (ETDEWEB)

Ng, C.Y.P. [Department of Physics and Materials Science, City University of Hong Kong (Hong Kong); Cheng, S.H., E-mail: bhcheng@cityu.edu.hk [Department of Biomedical Sciences, City University of Hong Kong (Hong Kong); State Key Laboratory in Marine Pollution, City University of Hong Kong (Hong Kong); Yu, K.N., E-mail: peter.yu@cityu.edu.hk [Department of Physics and Materials Science, City University of Hong Kong (Hong Kong); State Key Laboratory in Marine Pollution, City University of Hong Kong (Hong Kong)

2016-06-15

Highlights: • Studied hormetic effect induced by uranium (U) in embryos of zebrafish (Danio rerio). • Hormesis observed at 24 hpf for exposures to 10 μg/l of depleted U (DU). • Hormesis not observed before 30 hpf for exposures to 100 μg/l of DU. • Hormetic effect induced in zebrafish embryos in a dose-and time-dependent manner. - Abstract: The present work studied the hormetic effect induced by uranium (U) in embryos of zebrafish (Danio rerio) using apoptosis as the biological endpoint. Hormetic effect is characterized by biphasic dose-response relationships showing a low-dose stimulation and a high-dose inhibition. Embryos were dechorionated at 4 h post fertilization (hpf), and were then exposed to 10 or 100 μg/l depleted uranium (DU) in uranyl acetate solutions from 5 to 6 hpf. For exposures to 10 μg/l DU, the amounts of apoptotic signals in the embryos were significantly increased at 20 hpf but were significantly decreased at 24 hpf, which demonstrated the presence of U-induced hormesis. For exposures to 100 μg/l DU, the amounts of apoptotic signals in the embryos were significantly increased at 20, 24 and 30 hpf. Hormetic effect was not shown but its occurrence between 30 and 48 hpf could not be ruled out. In conclusion, hormetic effect could be induced in zebrafish embryos in a concentration- and time-dependent manner.

Use of depleted uranium silicate glass to minimize release of radionuclides from spent nuclear fuel waste packages

International Nuclear Information System (INIS)

Forsberg, C.W.

1996-01-01

A Depleted Uranium Silicate Container Backfill System (DUSCOBS) is proposed that would use small, isotopically-depleted uranium silicate glass beads as a backfill material inside repository waste packages containing spent nuclear fuel (SNF). The uranium silicate glass beads would fill the void space inside the package including the coolant channels inside SNF assemblies. Based on preliminary analysis, the following benefits have been identified. DUSCOBS improves repository waste package performance by three mechanisms. First, it reduces the radionuclide releases from SNF when water enters the waste package by creating a local uranium silicate saturated groundwater environment that suppresses (a) the dissolution and/or transformation of uranium dioxide fuel pellets and, hence, (b) the release of radionuclides incorporated into the SNF pellets. Second, the potential for long-term nuclear criticality is reduced by isotopic exchange of enriched uranium in SNF with the depleted uranium (DU) in the glass. Third, the backfill reduces radiation interactions between SNF and the local environment (package and local geology) and thus reduces generation of hydrogen, acids, and other chemicals that degrade the waste package system. Finally, DUSCOBS provides a potential method to dispose of significant quantities of excess DU from uranium enrichment plants at potential economic savings. DUSCOBS is a new concept. Consequently, the concept has not been optimized or demonstrated in laboratory experiments

The state of knowledge about the potential risks associated to depleted uranium used in weapons

International Nuclear Information System (INIS)

2001-01-01

This document brigs back the actual knowledge on uranium and its chemical and radiological toxicity. It pays particular attention to discuss the elements allowing to assess the risks linked to the man exposure to depleted uranium. (N.C.)

The frequency of chromosomal aberrations in sheep from the area contaminated by depleted uranium during NATO air strikes in 1999

Directory of Open Access Journals (Sweden)

Fišter Svetlana L.

2014-01-01

Full Text Available This paper presents the results of cytogenetic studies in sheep from the region of Bujanovac that was contaminated by depleted uranium during the NATO air strikes in 1999. The study was conducted on sheep blood lymphocytes, in order to determine the frequency of chromosomal aberrations and to assess the presence of genetic risk as a result of the possible impact of depleted uranium. Blood samples for lymphocyte cultures were taken at random from the 20 animals of the households in the village of Borovac, near Bujanovac. The animals were chosen because they were pastured, fed, and watered in the NATO bombing area. With the purpose of comparing the results two control groups were cytogenetically analyzed, each consisted of 20 sheep from Zemun and Ovča, two northern localities that were not contaminated with depleted uranium. The established structural chromosomal changes were of breaks and gap types, and their frequencies in sheep of all surveyed localities were within the range of basic level values that are commonly found in the sheep lymphocyte cultures analyses. Significant differences are apparent between the values defined in the sheep from Bujanovac compared to those obtained in the sheep from the northern locality (Zemun, probably as a result of breeding of animals in the farm conditions and their being less exposed to the impact of environmental agents. There were neither elevated values of polyploid and aneuploid cells nor significant differences between the sites. According to earlier known data, depleted uranium was below the detection limit of the method applied both in the soil and feed given to cytogenetically analyzed animals. Based on the low-level changes that are in the range of the basic level changes, commonly observed in sheep lymphocytes control cultures, it cannot be said with certainty that it was depleted uranium that caused the changes, or that it is wide-spread in the region of Bujanovac. [Projekat Ministarstva nauke

Processing and Applications of Depleted Uranium Alloy Products

Science.gov (United States)

1976-09-01

ammunition, weapons, gyrorotors, and ballast. Depleted uranium used in fly- wheel devices, nuclear fuel casks, and ammunition could consume a significant...from straight in the range of 0,002 to 0.060-inch TIR (total indicated runout ) with an average of 0.025-inch TIR.* Solution heat treatment of the as-cast...an envelope thickness of 0.050 inch to allow for runout and to clean up surface imperfections. The runout resulting from heat treatment was in the

Applications of Depleted Uranium in the first and second Persian Gulf Wars: a review article

Directory of Open Access Journals (Sweden)

Abdolhamid Behrouzi

2009-12-01

Full Text Available Background: Depleted uranium (DU is a byproduct of natural uranium enrichment process. Its unique characteristics (e.g. high density caused to use in civilian and military fields extensively. In the military fields, DU is used in the bullets and projectiles war hats. The munitions containing DU were used in the recent wars, more strikingly in the Middle East region (first and second Persian Gulf wars, and Afghanistan. Due to its biological impacts, this study aimed to assess biological effects of DU using scientometrics by investigating papers indexed in Pubmed from 1990-2008, to reveal the number and type of articles and also the important dimensions of DU biological impacts as well as the core issues. Methods: In this descriptive epidemiologic study, quantitative methods (counting frequency of words and scientometrics were used. Sample size was the total of the articles indexed in Pubmed during 1991- 2008, containing the terms "Gulf War" and "Depleted Uranium" in their title or keywords. Results: The most compromised body systems were urinary, nervous and cardiovascular. Other systems such as endocrine, musculoskeletal, immune and respiratory were also mentioned. Conclusion: Highly controversial results which have been stated in the surveyed articles about DU biological and environmental impacts caused the authors to recommend long term investigations for assessing its effects on recurrence to reveal potential late effects of DU.

Safety evaluation for packaging (onsite) depleted uranium waste boxes

Energy Technology Data Exchange (ETDEWEB)

McCormick, W.A.

1997-08-27

This safety evaluation for packaging (SEP) allows the one-time shipment of ten metal boxes and one wooden box containing depleted uranium material from the Fast Flux Test Facility to the burial grounds in the 200 West Area for disposal. This SEP provides the analyses and operational controls necessary to demonstrate that the shipment will be safe for the onsite worker and the public.

Safety evaluation for packaging (onsite) depleted uranium waste boxes

International Nuclear Information System (INIS)

McCormick, W.A.

1997-01-01

This safety evaluation for packaging (SEP) allows the one-time shipment of ten metal boxes and one wooden box containing depleted uranium material from the Fast Flux Test Facility to the burial grounds in the 200 West Area for disposal. This SEP provides the analyses and operational controls necessary to demonstrate that the shipment will be safe for the onsite worker and the public

Device for safe disposal of non-utilizable cuttings from depleted uranium metal

International Nuclear Information System (INIS)

Fiala, B.

1991-01-01

A device was developed for the production of U 3 O 8 from cuttings of depleted uranium metal or of uranium metal waste whose surface area is sufficiently large for combustion. The waste may contain organic impurities or other metals. The purity of the U 3 O 8 thus obtained is about 98%. Tests gave evidence that the combustion facility meets all requirements set forth by hygienic and ecological regulations. (Z.M.). 1 fig

American big dirty secret. About the depleted uranium weapons reality

International Nuclear Information System (INIS)

Parsons, R.J.

2002-01-01

From International organizations point of view, as the WHO, the hazard of the depleted uranium weapons use, is more and more obvious for the environment and the people health. The author shows how the USA military Government seems not really ''clean'' on this situation and denounces the danger of such a policy. (A.L.B.)

Properties, use and health effects of depleted uranium

International Nuclear Information System (INIS)

Aloraby, M.N.

2010-01-01

Depleted uranium (DU), a waste product of uranium enrichment, has several civilian and military applications. It was used as armor-piercing ammunition in international military conflicts and was claimed to contribute to health problems, known as the Gulf War Syndrome. This led to renewed efforts to assess the environmental consequences and health impact of DU use. The radiological and chemical properties of DU can be compared to those of natural uranium, which is ubiquitously present in soil at a typical concentration of 3 mg/kg. Natural uranium has the same chemo toxicity, but its radiotoxicity is 60% higher. Due to low specific radioactivity and the dominance of alpha radiation no acute risk is attributed to external exposure to DU. The major risk is DU dust, generated when DU ammunition hits hard targets. After deposition on the ground, resuspension takes place, if the DU containing particle size sufficiently small. However, transfer to drinking water or locally produced food has little potential to lead to significant exposure to DU. Since poor solubility of uranium compounds and lack of information on speciation precludes the use of radioecological models for exposure assessment, bio monitoring has to be used for assessing exposed persons. With the exception of crews of military vehicles having been hit by DU penetrators, no body burdens above the range of values for natural uranium have been found. Therefore, observable health effects are not expected and residual cancer risk estimates have to be based on theoretical considerations. They appear to be very minor for all post-conflict situations, i.e. a fraction of those expected from natural radiation. (author)

Transformation of human osteoblast cells to the tumorigenic phenotype by depleted uranium-uranyl chloride.

OpenAIRE

Miller, A C; Blakely, W F; Livengood, D; Whittaker, T; Xu, J; Ejnik, J W; Hamilton, M M; Parlette, E; John, T S; Gerstenberg, H M; Hsu, H

1998-01-01

Depleted uranium (DU) is a dense heavy metal used primarily in military applications. Although the health effects of occupational uranium exposure are well known, limited data exist regarding the long-term health effects of internalized DU in humans. We established an in vitro cellular model to study DU exposure. Microdosimetric assessment, determined using a Monte Carlo computer simulation based on measured intracellular and extracellular uranium levels, showed that few (0.0014%) cell nuclei...

Including environmental concerns in management strategies for depleted uranium hexafluoride

International Nuclear Information System (INIS)

Goldberg, M.; Avci, H.I.; Bradley, C.E.

1995-01-01

One of the major programs within the Office of Nuclear Energy, Science, and Technology of the US Department of Energy (DOE) is the depleted uranium hexafluoride (DUF 6 ) management program. The program is intended to find a long-term management strategy for the DUF 6 that is currently stored in approximately 46,400 cylinders at Paducah, KY; Portsmouth, OH; and Oak Ridge, TN, USA. The program has four major components: technology assessment, engineering analysis, cost analysis, and the environmental impact statement (EIS). From the beginning of the program, the DOE has incorporated the environmental considerations into the process of strategy selection. Currently, the DOE has no preferred alternative. The results of the environmental impacts assessment from the EIS, as well as the results from the other components of the program, will be factored into the strategy selection process. In addition to the DOE's current management plan, other alternatives continued storage, reuse, or disposal of depleted uranium, will be considered in the EIS. The EIS is expected to be completed and issued in its final form in the fall of 1997

Tungsten versus depleted uranium for armour-piercing penetrators

International Nuclear Information System (INIS)

Johnson, P.K.

1983-01-01

Tungsten alloys have been widely used in the production of armour-piercing (AP) penetrators for defense purposes for the past 40 years. In recent years, however, depleted uranium (DU) has also been utilised for this application. Both materials exhibit high density and strength, two properties necessary for kinetic-energy projectiles to penetrate armour on tanks and other vehicles. The facts, however, support the view that tungsten can and should be utilised as the primary material for most armour-defeating ordnance applications. (author)

800-MeV proton irradiation of thorium and depleted uranium targets

Energy Technology Data Exchange (ETDEWEB)

Russell, G.J.; Brun, T.O.; Pitcher, E.J. [Los Alamos National Laboratory, NM (United States)] [and others

1995-10-01

As part of the Los Alamos Fertile-to-Fissile-Conversion (FERFICON) program in the late 1980`s, thick targets of the fertile materials thorium and depleted uranium were bombarded by 800-MeV protons to produce the fissile materials {sup 233}U and {sup 239}Pu, respectively. The amount of {sup 233}U made was determined by measuring the {sup 233}Pa activity, and the yield of {sup 239}Pu was deduced by measuring the activity of {sup 239}Np. For the thorium target, 4 spallation products and 34 fission products were also measured. For the depleted uranium target, 3 spallation products and 16 fission products were also measured. The number of fissions in each target was deduced from fission product mass-yield curves. In actuality, axial distributions of the products were measured, and the distributions were then integrated over the target volume to obtain the total number of products for each reaction.

Radiological assessment of depleted uranium migration offsite from an ordnance range

International Nuclear Information System (INIS)

Rynders, D.G.

1996-01-01

The military utilizes ordnance loaded with depleted uranium in order to maximize armor penetrating capabilities. These weapons are tested on open ranges where the weapons are fired through a cloth target and impact into the soil. This paper examines the potential environmental impact from use of depleted uranium in an open setting. A preliminary pathway analysis was performed to examine potential routes of exposure to nonhuman species in the vicinity and ultimately to man. Generic data was used in the study to estimate the isotopic mix and weight of the ordnance. Key factors in the analysis included analyzing the physics of weapon impact on soil, chemical changes in material upon impact, and mechanisms of offsite transport (including atmospheric and overland transport). Non-standard exposure scenarios were investigated, including the possibility of offsite contaminant transport due to range grassfires. Two radiological assessment codes, MEPAS (Multi media Environmental Pollutant Assessment System) and RESRAD were used to help analyze the scenarios

Depleted uranium in Bosnia and Herzegovina. Post-conflict environmental assessment

International Nuclear Information System (INIS)

2003-03-01

Depleted Uranium (DU) ammunition was used in 1994-95 during the conflict in Bosnia and Herzegovina. This third DU field study from the Balkans, following UNEP's earlier DU studies in Kosovo (2001) and Serbia and Montenegro (2002), increases the scientific knowledge of the behaviour of DU in the environment. The mission investigated 14 sites. DU could be easily found at three of these sites more than seven years after the conflict and was confirmed by the physical presence of penetrators and jackets, as well as by soil, bio-indicator, water and air samples. For the first time in UNEP's DU studies in the Balkans, DU was found in drinking water samples, albeit at extremely low levels. DU was also measured in air samples, both outside as well as inside certain buildings currently in use. The report recommends precautionary steps in the form of decontamination and clean-up. Given the remaining scientific uncertainties on the long-term behaviour of DU in the natural environment, UNEP recommends further studies to be done in other regions where DU ammunition has been used. (author)

Absorption, accumulation and biological effects of depleted uranium in Peyer's patches of rats

International Nuclear Information System (INIS)

Dublineau, I.; Grison, S.; Grandcolas, L.; Baudelin, C.; Tessier, C.; Suhard, D.; Frelon, S.; Cossonnet, C.; Claraz, M.; Ritt, J.; Paquet, P.; Voisin, P.; Gourmelon, P.

2006-01-01

The digestive tract is the entry route for radionuclides following the ingestion of contaminated food and/or water wells. It was recently characterized that the small intestine was the main area of uranium absorption throughout the gastrointestinal tract. This study was designed to determine the role played by the Peyer's patches in the intestinal absorption of uranium, as well as the possible accumulation of this radionuclide in lymphoid follicles and the toxicological or pathological consequences on the Peyer's patch function subsequent to the passage and/or accumulation of uranium. Results of experiments performed in Ussing chambers indicate that the apparent permeability to uranium in the intestine was higher (10-fold) in the mucosa than in Peyer's patches ((6.21 ± 1.21 to 0.55 ± 0.35) x 10 -6 cm/s, respectively), demonstrating that the small intestinal epithelium was the preferential pathway for the transmucosal passage of uranium. A quantitative analysis of uranium by ICP-MS following chronic contamination with depleted uranium during 3 or 9 months showed a preferential accumulation of uranium in Peyer's patches (1355% and 1266%, respectively, at 3 and 9 months) as compared with epithelium (890% and 747%, respectively, at 3 and 9 months). Uranium was also detected in the mesenteric lymph nodes (∼5-fold after contamination with DU). The biological effects of this accumulation of depleted uranium after chronic contamination were investigated in Peyer's patches. There was no induction of the apoptosis pathway after chronic DU contamination in Peyer's patches. The results indicate no change in the cytokine expression (Il-10, TGF-β, IFN-γ, TNF-α, MCP-1) in Peyer's patches and in mesenteric lymph nodes, and no modification in the uptake of yeast cells by Peyer's patches. In conclusion, this study shows that the Peyer's patches were a site of retention for uranium following the chronic ingestion of this radionuclide, without any biological consequences of

Physicochemical Characterization of Capstone Depleted Uranium Aerosols III: Morphologic and Chemical Oxide Analyses

International Nuclear Information System (INIS)

Krupka, Kenneth M.; Parkhurst, MaryAnn; Gold, Kenneth; Arey, Bruce W.; Jenson, Evan D.; Guilmette, Raymond A.

2009-01-01

The impact of depleted uranium (DU) penetrators against an armored target causes erosion and fragmentation of the penetrators, the extent of which is dependent on the thickness and material composition of the target. Vigorous oxidation of the DU particles and fragments creates an aerosol of DU oxide particles and DU particle agglomerations combined with target materials. Aerosols from the Capstone DU aerosol study, in which vehicles were perforated by DU penetrators, were evaluated for their oxidation states using X-ray diffraction (XRD) and particle morphologies using scanning electron microscopy/energy dispersive spectrometry (SEM/EDS). The oxidation state of a DU aerosol is important as it offers a clue to its solubility in lung fluids. The XRD analysis showed that the aerosols evaluated were a combination primarily of U3O8 (insoluble) and UO3 (relatively more soluble) phases, though intermediate phases resembling U4O9 and other oxides were prominent in some samples. Analysis of particle residues in the micrometer-size range by SEM/EDS provided microstructural information such as phase composition and distribution, fracture morphology, size distribution, and material homogeneity. Observations from SEM analysis show a wide variability in the shapes of the DU particles. Some of the larger particles appear to have been fractured (perhaps as a result of abrasion and comminution); others were spherical, occasionally with dendritic or lobed surface structures. Amorphous conglomerates containing metals other than uranium were also common, especially with the smallest particle sizes. A few samples seemed to contain small chunks of nearly pure uranium metal, which were verified by EDS to have a higher uranium content exceeding that expected for uranium oxides. Results of the XRD and SEM/EDS analyses were used in other studies described in this issue of The Journal of Health Physics to interpret the results of lung solubility studies and in selecting input parameters for

Using depleted uranium to shield vitrified high-level waste packages

International Nuclear Information System (INIS)

Yoshimura, H.R.; Gildea, P.D.; Bernard, E.A.

1995-01-01

The underlying report for this paper evaluates options for using depleted uranium as shielding materials for transport systems for disposal of vitrified high-level waste (VHLW). In addition, economic analyses are presented to compare costs associated with these options to costs, associated with existing and proposed storage, transport, and diposal capabilities. A more detailed evaluation is provided elsewhere. (Yoshimura et al. 1995.)

Final programmatic environmental impact statement for alternative strategies for the long-term management and use of depleted uranium hexafluoride. Summary

International Nuclear Information System (INIS)

1999-04-01

This PEIS assesses the potential impacts of alternative management strategies for depleted uranium hexafluoride (UF 6 ) currently stored at three DOE sites: Paducah site near Paducah, Kentucky, Portsmouth site near Portsmouth, Ohio; and K-25 site on the Oak Ridge Reservation, Oak Ridge, Tennessee. The alternatives analyzed in the PEIS include no action, long-term storage as UF 6 , long-term storage as uranium oxide, use as uranium oxide, use as uranium metal, and disposal. DOE's preferred alternative is to begin conversion of the depleted UF 6 inventory as soon as possible, either to uranium oxide, uranium metal, or a combination of both, while allowing for use of as much of this inventory as possible

Regulatory considerations and quality assurance of depleted uranium based radiography cameras

International Nuclear Information System (INIS)

Sapkal, Jyotsna A.; Yadav, R.K.B.; Amrota, C.T.; Singh, Pratap; GopaIakrishanan, R.H.; Patil, B.N.; Mane, Nilesh

2016-01-01

Radiography cameras with shielding material as Depleted Uranium (DU) are used for containment of Iridium ( 192 Ir) source. DU shielding surrounds the titanium made 'S' tube through which the encapsulated 192 Ir source along with the pigtail travels. As per guidelines, it is required to check periodically the shielding integrity of DU shielding periodically by monitoring for alpha transferable contamination inside the 'S' tube. This paper describes in brief the method followed for collection of samples from inside the 'S' tube . The samples were analysed for transferable contamination due to gross alpha using alpha scintillation (ALSCIN) counter. The gross alpha contamination in the 'S' tube was found to be less than the recommended USNRC value for discarding the radiography camera. IAEA recommendations related to transferable contamination and AERB guidelines on the quality assurance (QA) requirements of radiography camera were studied

Uranium tailings sampling manual

International Nuclear Information System (INIS)

Feenstra, S.; Reades, D.W.; Cherry, J.A.; Chambers, D.B.; Case, G.G.; Ibbotson, B.G.

1985-01-01

The purpose of this manual is to describe the requisite sampling procedures for the application of uniform high-quality standards to detailed geotechnical, hydrogeological, geochemical and air quality measurements at Canadian uranium tailings disposal sites. The selection and implementation of applicable sampling procedures for such measurements at uranium tailings disposal sites are complicated by two primary factors. Firstly, the physical and chemical nature of uranium mine tailings and effluent is considerably different from natural soil materials and natural waters. Consequently, many conventional methods for the collection and analysis of natural soils and waters are not directly applicable to tailings. Secondly, there is a wide range in the physical and chemical nature of uranium tailings. The composition of the ore, the milling process, the nature of tailings depositon, and effluent treatment vary considerably and are highly site-specific. Therefore, the definition and implementation of sampling programs for uranium tailings disposal sites require considerable evaluation, and often innovation, to ensure that appropriate sampling and analysis methods are used which provide the flexibility to take into account site-specific considerations. The following chapters describe the objective and scope of a sampling program, preliminary data collection, and the procedures for sampling of tailings solids, surface water and seepage, tailings pore-water, and wind-blown dust and radon

Oxidation experiment of metal uranium waste for the treatment of depleted uranium waste

International Nuclear Information System (INIS)

Kang, K. H.; Kwac, K. I.; Kim, K. J.

2001-01-01

A study was conducted on the oxidation behavior of U-Ti chips(Depleted Uranium, DU chips) using an XRD and a thermogravimetric analyzer in the temperature range from 250 to 500 .deg. C in air. At the temperature lower than 400 .deg. C, DU chips were converted to UO 2 , U 3 O 7 and U 3 O 8 whereas at the temperature higher than 400 .deg. C, DU chips were completely converted to U 3 O 8 , the most stable form of uranium oxide. The activation energy for the oxidation of U-Ti chips is found, 44.9 kJ/mol and the oxidation rate in terms of weight gain (%) can be expressed as ; dW/dt=8.4 x 10 2 e(-44.9 kJ/mol /RT) wt %/min (250≤T(deg. C)≤500) where W=weight gain (%), t=time and T=temperature

Long-term ecological effects of exposure to uranium

International Nuclear Information System (INIS)

Hanson, W.C.; Miera, F.R. Jr.

1976-03-01

The consequences of releasing natural and depleted uranium to terrestrial ecosystems during development and testing of depleted uranium munitions were investigated. At Eglin Air Force Base, Florida, soil at various distances from armor plate target butts struck by depleted uranium penetrators was sampled. The upper 5 cm of soil at the target bases contained an average of 800 ppM of depleted uranium, about 30 times as much as soil at 5- to 10-cm depth, indicating some vertical movement of depleted uranium. Samples collected beyond about 20 m from the targets showed near-background natural uranium levels, about 1.3 +- 0.3 μg/g or ppM. Two explosives-testing areas at the Los Alamos Scientific Laboratory (LASL) were selected because of their use history. E-F Site soil averaged 2400 ppM of uranium in the upper 5 cm and 1600 ppM at 5-10 cm. Lower Slobovia Site soil from two subplots averaged about 2.5 and 0.6 percent of the E-F Site concentrations. Important uranium concentration differences with depth and distance from detonation points were ascribed to the different explosive tests conducted in each area. E-F Site vegetation samples contained about 320 ppM of uranium in November 1974 and about 125 ppM in June 1975. Small mammals trapped in the study areas in November contained a maximum of 210 ppM of uranium in the gastrointestinal tract contents, 24 ppM in the pelt, and 4 ppM in the remaining carcass. In June, maximum concentrations were 110, 50, and 2 ppM in similar samples and 6 ppM in lungs. These data emphasized the importance of resuspension of respirable particles in the upper few millimeters of soil as a contamination mechanism for several components of the LASL ecosystem

Depleted uranium hexafluoride (DUF6) management system--a decision tool

International Nuclear Information System (INIS)

Gasper, J.R.; Sutter, R.J.; Avci, H.I.

1995-01-01

The Depleted Uranium Hexafluoride (DUF 6 ) Management System (DMS) is being developed as a decision tool to provide cost and risk data for evaluation of short-and long-term management strategies for depleted uranium. It can be used to assist decision makers on a programmatic or site-specific level. Currently, the DMS allows evaluation of near-term cylinder management strategies such as storage yard improvements, cylinder restocking, and reconditioning. The DMS has been designed to provide the user with maximum flexibility for modifying data and impact factors (e.g., unit costs and risk factors). Sensitivity analysis can be performed on all key parameters such as cylinder corrosion rate, inspection frequency, and impact factors. Analysis may be conducted on a system-wide, site, or yard basis. The costs and risks from different scenarios may be compared in graphic or tabular format. Ongoing development of the DMS will allow similar evaluation of long-term management strategies such as conversion to other chemical forms. The DMS is a Microsoft Windows 3.1 based, stand-alone computer application. It can be operated on a 486 or faster computer with VGA, 4 MB of RAM, and 10 MB of disk space

Radiological air quality in a depleted uranium (DU) storage vault

International Nuclear Information System (INIS)

Robinson, T.; Cucchiara, A.L.

1999-01-01

The radiological air quality of two storage vaults, one with depleted uranium (DU) and one without, was evaluated and compared. The intent of the study was to determine if the presence of stored DU would significantly contribute to the gaseous/airborne radiation level compared to natural background. Both vaults are constructed out of concrete and are dimensionally similar. The vaults are located on the first floor of the same building. Neither vault has air supply or air exhaust. The doors to both vaults remained closed during the evaluation period, except for brief and infrequent access by the operational group. One vault contained 700 KG of depleted uranium, and the other vault contained documents inside of file cabinets. Radon detectors and giraffe air samplers were used to gather data on the quantity of gaseous/airborne radionuclides in both vaults. The results of this study indicated that there was no significant difference in the quantity of gaseous/airborne radionuclides in the two vaults. This paper gives a discussion of the effects of the stored DU on the air quality, and poses several theories supporting the results

Comparative study of femtosecond and nanosecond laser-induced breakdown spectroscopy of depleted uranium

International Nuclear Information System (INIS)

Emmert, Luke A.; Chinni, Rosemarie C.; Cremers, David A.; Jones, C. Randy; Rudolph, Wolfgang

2011-01-01

We present spectra of depleted uranium metal from laser plasmas generated by nanosecond Nd:YAG (1064 nm) and femtosecond Ti:sapphire (800 nm) laser pulses. The latter pulses produce short-lived and relatively cool plasmas in comparison to the longer pulses, and the spectra of neutral uranium atoms appear immediately after excitation. Evidence for nonequilibrium excitation with femtosecond pulses is found in the dependence of spectral line intensities on the pulse chirp.

Laser-induced breakdown spectroscopy measurements of uranium and thorium powders and uranium ore

Energy Technology Data Exchange (ETDEWEB)

Judge, Elizabeth J. [Chemistry Division, Los Alamos National Laboratory, Los Alamos, NM 87545 (United States); Barefield, James E., E-mail: jbarefield@lanl.gov [Chemistry Division, Los Alamos National Laboratory, Los Alamos, NM 87545 (United States); Berg, John M. [Manufacturing Engineering and Technology Division, Los Alamos National Laboratory, Los Alamos, NM 87545 (United States); Clegg, Samuel M.; Havrilla, George J.; Montoya, Velma M.; Le, Loan A.; Lopez, Leon N. [Chemistry Division, Los Alamos National Laboratory, Los Alamos, NM 87545 (United States)

2013-05-01

Laser-induced breakdown spectroscopy (LIBS) was used to analyze depleted uranium and thorium oxide powders and uranium ore as a potential rapid in situ analysis technique in nuclear production facilities, environmental sampling, and in-field forensic applications. Material such as pressed pellets and metals, has been extensively studied using LIBS due to the high density of the material and more stable laser-induced plasma formation. Powders, on the other hand, are difficult to analyze using LIBS since ejection and removal of the powder occur in the laser interaction region. The capability of analyzing powders is important in allowing for rapid analysis of suspicious materials, environmental samples, or trace contamination on surfaces since it most closely represents field samples (soil, small particles, debris etc.). The rapid, in situ analysis of samples, including nuclear materials, also reduces costs in sample collection, transportation, sample preparation, and analysis time. Here we demonstrate the detection of actinides in oxide powders and within a uranium ore sample as both pressed pellets and powders on carbon adhesive discs for spectral comparison. The acquired LIBS spectra for both forms of the samples differ in overall intensity but yield a similar distribution of atomic emission spectral lines. - Highlights: • LIBS analysis of mixed actinide samples: depleted uranium oxide and thorium oxide • LIBS analysis of actinide samples in powder form on carbon adhesive discs • Detection of uranium in a complex matrix (uranium ore) as a precursor to analyzing uranium in environmental samples.

Patch testing with uranyl acetate in veterans exposed to depleted uranium during the 1991 Gulf war and the Iraqi conflict.

Science.gov (United States)

Shvartsbeyn, Marianna; Tuchinda, Papapit; Gaitens, Joanna; Squibb, Katherine S; McDiarmid, Melissa A; Gaspari, Anthony A

2011-01-01

The Depleted Uranium Follow-Up Program is a clinical surveillance program run by the Baltimore Veterans Affairs Medical Center since 1993 for veterans of the Gulf and Iraqi wars who were exposed to depleted uranium (DU) as a result of "friendly-fire" incidents. In 2009, 40 veterans from this cohort were screened for skin reactivity to metals by patch-testing with extended metal series and uranyl acetate (0.25%, 2.5%, and 25%). A control arm comprised 46 patients without any known occupational exposures to DU who were seen at the University of Maryland Dermatology Clinic for evaluation of allergic contact dermatitis. Excluding irritant reactions, no patch-test reactions to uranyl acetate were observed in the participants. Irritant reactions to DU were more common in the clinic cohort, likely reflective of the demographic differences between the two arms of the study. Biologic monitoring of urine uranium concentrations in the DU program participants with 24-hour urine samples showed evidence of percutaneous uranium absorption from the skin patches. We conclude that dermatitis observed in a subset of the veterans was unrelated to their military DU exposure. Our data suggest that future studies of skin testing with uranyl acetate should utilize 0.25%, the least irritating concentration.

The crystallographic structure of the air-grown oxide on depleted uranium metal

International Nuclear Information System (INIS)

Jones, Christopher P.; Petherbridge, James R.; Davis, Sean A.; Jones, Jonathon A.; Scott, Thomas B.

2016-01-01

Highlights: • Oxidation of depleted uranium coupons under ambient conditions and 150 °C. • Oxide characterised using SEM, TEM and electron backscatter diffraction analysis, • Layer comprises of UO 2 crystallites 12 nm in diameter. • Preferred [110] growth direction normal to the surface of the metal. • Oxide growth direction is independent of the underlying crystal orientation. - Abstract: Oxide formation on depleted uranium metal was investigated using a combination of electron backscatter diffraction (EBSD) and transmission electron microscopy (TEM) characterisation. Diffraction analysis of the oxide revealed an FCC crystalline formation of UO 2 crystallites whilst TEM data indicated an average grain size of 12 nm with a standard deviation of 3.8 nm. EBSD analysis revealed a preferential texture of [110] normal to the surface of the metal. This data implied that lattice matching between the oxide and the underlying metal did not occur, therefore, the observed preferential growth direction is independent of the underlying crystal orientation.

Assessment of the environmental radioactive contamination levels by depleted uranium after NATO aggression on FR Yugoslavia

International Nuclear Information System (INIS)

Pavlovic, S.; Pavlovic, R.; Markovic, S; Plecas, I.

2001-01-01

During NATO aggression on FR Yugoslavia various ammunition have been used, some of them for the first time. Among others, 30 mm bullets with depleted uranium (DU) penetrators have been used. Radioactivity contamination surveys have started during the war due to indications that DU is used in cruise missiles. Besides that, there were a lot of radioactivity analysis of food, drinking water etc. Some of the obtained results are presented in this paper. Depleted uranium ammunition can permanently contaminate environment and so produce effects on population. Relation of the international radiation and environmental protection standards and contamination levels are discussed as well. (author)

Measurement of thermal diffusivity of depleted uranium metal microspheres

Science.gov (United States)

Humrickhouse-Helmreich, Carissa J.; Corbin, Rob; McDeavitt, Sean M.

2014-03-01

The high void space of nuclear fuels composed of homogeneous uranium metal microspheres may allow them to achieve ultra-high burnup by accommodating fuel swelling and reducing fuel/cladding interactions; however, the relatively low thermal conductivity of microsphere nuclear fuels may limit their application. To support the development of microsphere nuclear fuels, an apparatus was designed in a glovebox and used to measure the apparent thermal diffusivity of a packed bed of depleted uranium (DU) microspheres with argon fill in the void spaces. The developed Crucible Heater Test Assembly (CHTA) recorded radial temperature changes due to an initial heat pulse from a central thin-diameter cartridge heater. Using thermocouple positions and time-temperature data, the apparent thermal diffusivity was calculated. The thermal conductivity of the DU microspheres was calculated based on the thermal diffusivity from the CHTA, known material densities and specific heat capacities, and an assumed 70% packing density based on prior measurements. Results indicate that DU metal microspheres have very low thermal conductivity, relative to solid uranium metal, and rapidly form an oxidation layer even in a low oxygen environment. At 500 °C, the thermal conductivity of the DU metal microsphere bed was 0.431 ± 0.0560 W/m-K compared to the literature value of approximately 32 W/m-K for solid uranium metal.

Measurement of thermal diffusivity of depleted uranium metal microspheres

Energy Technology Data Exchange (ETDEWEB)

Humrickhouse-Helmreich, Carissa J., E-mail: carissahelmreich@tamu.edu [Texas A and M University, Department of Nuclear Engineering, 337 Zachry Engineering Center, 3133 TAMU, College Station, TX 77843 (United States); Corbin, Rob, E-mail: rcorbin@terrapower.com [TerraPower, LLC, 330 120th Ave NE, Suite 100, Bellevue, WA 98005 (United States); McDeavitt, Sean M., E-mail: mcdeavitt@tamu.edu [Texas A and M University, Department of Nuclear Engineering, 337 Zachry Engineering Center, 3133 TAMU, College Station, TX 77843 (United States)

2014-03-15

The high void space of nuclear fuels composed of homogeneous uranium metal microspheres may allow them to achieve ultra-high burnup by accommodating fuel swelling and reducing fuel/cladding interactions; however, the relatively low thermal conductivity of microsphere nuclear fuels may limit their application. To support the development of microsphere nuclear fuels, an apparatus was designed in a glovebox and used to measure the apparent thermal diffusivity of a packed bed of depleted uranium (DU) microspheres with argon fill in the void spaces. The developed Crucible Heater Test Assembly (CHTA) recorded radial temperature changes due to an initial heat pulse from a central thin-diameter cartridge heater. Using thermocouple positions and time–temperature data, the apparent thermal diffusivity was calculated. The thermal conductivity of the DU microspheres was calculated based on the thermal diffusivity from the CHTA, known material densities and specific heat capacities, and an assumed 70% packing density based on prior measurements. Results indicate that DU metal microspheres have very low thermal conductivity, relative to solid uranium metal, and rapidly form an oxidation layer even in a low oxygen environment. At 500 °C, the thermal conductivity of the DU metal microsphere bed was 0.431 ± 0.0560 W/m-K compared to the literature value of approximately 32 W/m-K for solid uranium metal.

Measurement of thermal diffusivity of depleted uranium metal microspheres

International Nuclear Information System (INIS)

Humrickhouse-Helmreich, Carissa J.; Corbin, Rob; McDeavitt, Sean M.

2014-01-01

The high void space of nuclear fuels composed of homogeneous uranium metal microspheres may allow them to achieve ultra-high burnup by accommodating fuel swelling and reducing fuel/cladding interactions; however, the relatively low thermal conductivity of microsphere nuclear fuels may limit their application. To support the development of microsphere nuclear fuels, an apparatus was designed in a glovebox and used to measure the apparent thermal diffusivity of a packed bed of depleted uranium (DU) microspheres with argon fill in the void spaces. The developed Crucible Heater Test Assembly (CHTA) recorded radial temperature changes due to an initial heat pulse from a central thin-diameter cartridge heater. Using thermocouple positions and time–temperature data, the apparent thermal diffusivity was calculated. The thermal conductivity of the DU microspheres was calculated based on the thermal diffusivity from the CHTA, known material densities and specific heat capacities, and an assumed 70% packing density based on prior measurements. Results indicate that DU metal microspheres have very low thermal conductivity, relative to solid uranium metal, and rapidly form an oxidation layer even in a low oxygen environment. At 500 °C, the thermal conductivity of the DU metal microsphere bed was 0.431 ± 0.0560 W/m-K compared to the literature value of approximately 32 W/m-K for solid uranium metal

A dark side of the fuel cycle: some military uses of depleted uranium and potential consequences

International Nuclear Information System (INIS)

Andrews, W.S.; Lewis, B.J.; Bennett, L.G.I.; Ough, E.A.

2001-01-01

Over the past quarter century, depleted uranium (DU) has replaced tungsten alloys as the material of choice for penetrators in armour piercing rounds, in some armies, as well as a supplement to steel in tank armour. The tendency for adiabatic shear failure to overcome work hardening, and increased ductility are attributed for the improved ballistic performance. The aerosolization of a portion of the penetrator on impact creates a potential health hazard, particularly through ingesting resuspended aerosol particles. Bioassays of US and Canadian servicemen, potentially exposed to DU contamination, have failed to establish a link between DU and symptoms of 'Gulf War illness'. Further, Canadian testing has not been able to identify elevated levels of DU or even natural uranium in urine, hair or bone samples of veterans. (author)

Characterization of depleted uranium oxides fabricated using different processing methods

International Nuclear Information System (INIS)

Hastings, E.P.; Lewis, C.; FitzPatrick, J.; Rademacher, D.; Tandon, L.

2008-01-01

Identifying both physical and chemical characteristics of Special Nuclear Material (SNM) production processes is the corner stone of nuclear forensics. Typically, processing markers are based on measuring an interdicted sample's bulk chemical properties, such as the elemental or isotopic composition, or focusing on the chemical and physical morphology of only a few particles. Therefore, it is imperative that known SNM processes be fully characterized from bulk to trace level for each particle size range. This report outlines a series of particle size measurements and fractionation techniques that can be applied to a bulk SNM powders, categorizing both chemical and physical properties in discrete particle size fractions. This will be demonstrated by characterizing the process signatures of a series of different depleted uranium oxides prepared at increasing firing temperatures (350-1100 deg C). Results will demonstrate how each oxides' material density, particle size distribution, and morphology varies. (author)

The brain is a target organ after acute exposure to depleted uranium.

Science.gov (United States)

Lestaevel, P; Houpert, P; Bussy, C; Dhieux, B; Gourmelon, P; Paquet, F

2005-09-01

The health effects of depleted uranium (DU) are mainly caused by its chemical toxicity. Although the kidneys are the main target organs for uranium toxicity, uranium can also reach the brain. In this paper, the central effects of acute exposure to DU were studied in relation to health parameters and the sleep-wake cycle of adult rats. Animals were injected intraperitoneally with 144+/-10 microg DU kg-1 as nitrate. Three days after injection, the amounts of uranium in the kidneys represented 2.6 microg of DU g-1 of tissue, considered as a sub-nephrotoxic dosage. The central effect of uranium could be seen through a decrease in food intake as early as the first day after exposure and shorter paradoxical sleep 3 days after acute DU exposure (-18% of controls). With a lower dosage of DU (70+/-8 microg DU kg-1), no significant effect was observed on the sleep-wake cycle. The present study intends to illustrate the fact that the brain is a target organ, as are the kidneys, after acute exposure to a moderate dosage of DU. The mechanisms by which uranium causes these early neurophysiological perturbations shall be discussed.

Depleted uranium and radiation - induced lung cancer and leukaemia

International Nuclear Information System (INIS)

Mould, R.F.

2002-01-01

Reports of leukaemias and other cancers among servicemen who took part in the 1991 Gulf war or in the more recent operations in the Balkans are of continuing interest, as is the possibility, however slight, that depleted uranium (DU) is one of the causative factors. This commentary includes the results of a UK epidemiological study on the mortality of Gulf war veterans and , although not containing information on DU exposure, gives data on overall levels of mortality and therefore carries more weight than anecdotal reports. Also included are brief summaries on radiation-induced lung cancer in uranium workers as well as radiation-induced leukaemia in Japanese atomic bomb survivors and patients ankylosing spondylitis treated using x-rays. This commentary concludes with a critique of Iraqi cancer statistics as well as giving information on environmental contamination in Kosovo and the use of DU ammunition. (author)

Excretion of depleted uranium by Gulf war veterans

International Nuclear Information System (INIS)

Toohey, R.E.

2003-01-01

During the Persian Gulf War, in 1991, approximately 100 US military personnel had potential intakes of depleted uranium (DU), including shrapnel wounds. In 1993, the US government initiated a follow-up study of 33 Gulf War veterans who had been exposed to DU, many of whom contained embedded fragments of DU shrapnel in their bodies. The veterans underwent medical evaluation, whole-body counting, and urinalysis for uranium by kinetic phosphorescence analysis (KPA). Data are available from seven individuals who exceeded the detection limit for whole-body counting and also had elevated urinary uranium. Urinary excretion rates, in μg U g -1 creatinine, were determined in 1997 and 1999. The body contents, in mg DU, were determined in 1997; it is assumed there were no significant decreases in total body content in the interim. For the 1997 data, the mean fractional excretion was (2.4 ± 2.8) x 10 -5 g -1 creatinine, and for the 1999 data, the mean was (1.1 ± 0.6) x 10 -5 g -1 creatinine. However, these means are not significantly different, nor is there any correlation of excretion rate with body content. Thus, human data available to date do not provide any basis for determining the effects of particle surface area, composition and solubility, and biological processes such as encapsulation, on the excretion rate. (author)

Assessment of the Risks from Imbedded Fragments of Depleted Uranium

Science.gov (United States)

1993-03-01

for chronic kidney toxicity; the impact of fibrotic encapsulation , if it occurs; and the chemical form of the imbedded fragment. The potential for...Effects of Depleted Uranium Imbedded in Tissue Reference: Brigadier General Ronald R. Blanck (SGPS-PSP) letter of 26 February 1992 In response to your...the muscle and fatty tissue will probably occur and will occur in all other tissue types that elicit similar cellular responses to foreign bodies. It

Physicochemical characterization of Capstone depleted uranium aerosols III: morphologic and chemical oxide analyses.

Science.gov (United States)

Krupka, Kenneth M; Parkhurst, Mary Ann; Gold, Kenneth; Arey, Bruce W; Jenson, Evan D; Guilmette, Raymond A

2009-03-01

The impact of depleted uranium (DU) penetrators against an armored target causes erosion and fragmentation of the penetrators, the extent of which is dependent on the thickness and material composition of the target. Vigorous oxidation of the DU particles and fragments creates an aerosol of DU oxide particles and DU particle agglomerations combined with target materials. Aerosols from the Capstone DU aerosol study, in which vehicles were perforated by DU penetrators, were evaluated for their oxidation states using x-ray diffraction (XRD), and particle morphologies were examined using scanning electron microscopy/energy dispersive spectroscopy (SEM/EDS). The oxidation state of a DU aerosol is important as it offers a clue to its solubility in lung fluids. The XRD analysis showed that the aerosols evaluated were a combination primarily of U3O8 (insoluble) and UO3 (relatively more soluble) phases, though intermediate phases resembling U4O9 and other oxides were prominent in some samples. Analysis of particle residues in the micrometer-size range by SEM/EDS provided microstructural information such as phase composition and distribution, fracture morphology, size distribution, and material homogeneity. Observations from SEM analysis show a wide variability in the shapes of the DU particles. Some of the larger particles were spherical, occasionally with dendritic or lobed surface structures. Others appear to have fractures that perhaps resulted from abrasion and comminution, or shear bands that developed from plastic deformation of the DU material. Amorphous conglomerates containing metals other than uranium were also common, especially with the smallest particle sizes. A few samples seemed to contain small bits of nearly pure uranium metal, which were verified by EDS to have a higher uranium content exceeding that expected for uranium oxides. Results of the XRD and SEM/EDS analyses were used in other studies described in this issue of Health Physics to interpret the

Development of DU-AGG (Depleted Uranium Aggregate)

Energy Technology Data Exchange (ETDEWEB)

Lessing, P.A.

1995-09-01

Depleted uranium oxide (UO{sub 2} or U0{sub 3}) powder was mixed with fine mineral additives, pressed, and heated to about 1,250{degree}C. The additives were chemically constituted to result in an iron-enriched basalt (IEB). Melting and wetting of the IEB phase caused the urania powder compact to densify (sinter) via a liquid phase sintering mechanism. An inorganic lubricant was found to aid in green-forming of the body. Sintering was successful in oxidizing (air), inert (argon), or reducing (dry hydrogen containing) atmospheres. The use of ground U0{sub 3} powders (93 vol %) followed by sintering in a dry hydrogen-containing atmosphere significantly increased the density of samples (bulk density of 8.40 g/cm{sup 3} and apparent density of 9.48 g/cm{sup 3}, open porosity of 11.43%). An improvement in the microstructure (reduction in open porosity) was achieved when the vol % of U0{sub 3} was decreased to 80%. The bulk density increased to 8.59 g/cm{sup 3}, the apparent density decreased slightly to 8.82 g/cm{sup 3} (due to increase of low density IEB content), while the open porosity decreased to an excellent number of 2.78%. A representative sample derived from 80 vol % U0{sub 3} showed that most pores were closed pores and that, overall, the sample achieved the excellent relative density value of 94.1% of the estimated theoretical density (composite of U0{sub 2} and IEB). It is expected that ground powders of U0{sub 3} could be successfully used to mass produce lowcost aggregate using the green-forming technique of briquetting.

Incentives for the use of depleted uranium alloys as transport cask containment structure

International Nuclear Information System (INIS)

McConnell, P.; Salzbrenner, R.; Wellman, G.W.; Sorenson, K.B.

1992-01-01

Radioactive material transport casks use either lead or depleted uranium (DU) as gamma-ray shielding material. Stainless steel is conventionally used for structural containment. If a DU alloy had sufficient properties to guarantee resistance to failure during both nominal use and accident conditions to serve the dual-role of shielding and containment, the use of other structure materials (i.e., stainless steel) could be reduced. (It is recognized that lead can play no structural role.) Significant reductions in cask weight and dimensions could then be achieved perhaps allowing an increase in payload. The mechanical response of depleted uranium has previously not been included in calculations intended to show that DU-shielded transport casks will maintain their containment function during all conditions. This paper describesa two-part study of depleted uranium alloys: First, the mechanical behavior of DU alloys was determined in order to extend the limited set of mechanical properties reported in the literature. The mechanical properties measured include the tensile behavior the impact energy. Fracture toughness testing was also performed to determine the sensitivity of DU alloys to brittle fracture. Fracture toughness is the inherent material property which quantifies the fracmm resistance of a material. Tensile strength and ductility are significant in terms of other failure modes, however, as win be discussed. These mechanical properties were then input into finite element calculations of cask response to loading conditions to quantify the potential for claiming structural credit for DU. (The term ''structural credit'' describes whether a material has adequate properties to allow it to assume a positive role in withstanding structural loadings.)

Excavation and internment of depleted uranium and thorium soils, AHMC Jonesboro, Tennessee

International Nuclear Information System (INIS)

Bernhardt, D.E.; Prewett, S.V.; Boddy, J.R.

1986-01-01

This report describes the construction activities for the rockfilled berm and the excavation and disposal of contaminated soil, and the activities to certify the adequacy of the remedial activities. It focuses on the final closure. Mishu and Prewett in a paper in this proceeding provide additional information of the rockfilled wall. The final phase of the remedial program, referred to as the pond closure project, encompassed excavation of contaminated soil from the pond site and entombment of the waste in an encapsulating clay cell. The disposal cell was located at the pond site, and was situated above the level of the projected 100- and 500-year floods from Little Limestone Creek, which is adjacent to the site. The cell was built by completely enclosing the contaminated soil in a compacted clay liner and covering it with a compacted clay cap, each having a minimum thickness of four feet. Contaminated soil from the pond area and Aerojet Heavy Metals Company (AHMC) completed the remedial program for an inactive evaporation pond at its facility near Jonesboro, Tennessee during the summer of 1985. The pond had been used for process liquid wastes containing depleted uranium and thorium. Depleted uranium is a by-product of uranium richment, does not refer to use in a reactor, and does not contain Ra-226 or the associated decay products

Use of depleted uranium in military conflicts and possible post-conflict chemical and radiological risk to health and the environment

International Nuclear Information System (INIS)

Snihs, Jan Olof; Akerblom, Gustav

2000-01-01

During and after the Balkans conflict in 1999 there were rumours that so-called depleted uranium (DU) had been used in military operations by NATO. Attention was drawn to this issue by a number of countries, and consequently, there is a concern amongst the people of Serbia and Kosovo regarding the possible post-conflict chemical and radiological risk to health and the environment. The UN also has to deal with such concerns from the point of view of security of UN staff in the field. UNEP/Habitat Balkans Task Force (BTF) has been set up to make an overall assessment of the environmental consequences of the conflict and impacts of the conflict on human settlements in Kosovo, Macedonia, Montenegro, Albania and in Serbia. The work was done by organising Technical Missions to provide independent and reliable information which is relevant for the problem under consideration. As regards depleted uranium, a special international expert group, the 'Depleted Uranium Desk Assessment Group' was appointed to analyse and assess the situation. The group was chaired by Snihs. Since little or no information was available on the actual use of depleted uranium in the Kosovo conflict, the expert group was reduced to using available information from the 1990 Gulf conflict and published data on the risks of depleted uranium. It was possible to organise only one visit to Kosovo during the time available for this study, and that visit did not give any indications of contamination from depleted uranium. However, this does not exclude the possibility that there are DU-contaminated areas in Kosovo. By using basic facts relevant for risk assessment and making assumptions about the conditions for exposure to depleted uranium, that are as accurate as possible, it has been possible to assess likely consequences for health and environment. In case of uncertainties in the assumptions, conservative values have been used. On the basis of the conclusions of the assessments there are a number of

Final programmatic environmental impact statement for alternative strategies for the long-term management and use of depleted uranium hexafluoride. Volume 2: Appendices

International Nuclear Information System (INIS)

1999-04-01

This PEIS assesses the potential impacts of alternative management strategies for depleted uranium hexafluoride (UF 6 ) currently stored at three DOE sites: Paducah site near Paducah, Kentucky, Portsmouth site near Portsmouth, Ohio; and K-25 site on the Oak Ridge Reservation, Oak Ridge, Tennessee. The alternatives analyzed in the PEIS include no action, long-term storage as UF 6 , long-term storage as uranium oxide, use as uranium oxide, use as uranium metal, and disposal. DOE's preferred alternative is to begin conversion of the depleted UF 6 inventory as soon as possible, either to uranium oxide, uranium metal, or a combination of both, while allowing for use of as much of this inventory as possible. This volume contains Appendices A--O

The brain is a target organ after acute exposure to depleted uranium

International Nuclear Information System (INIS)

Lestaevel, P.; Houpert, P.; Bussy, C.; Dhieux, B.; Gourmelon, P.; Paquet, F.

2005-01-01

The health effects of depleted uranium (DU) are mainly caused by its chemical toxicity. Although the kidneys are the main target organs for uranium toxicity, uranium can also reach the brain. In this paper, the central effects of acute exposure to DU were studied in relation to health parameters and the sleep-wake cycle of adult rats. Animals were injected intraperitoneally with 144 ± 10 μg DU kg -1 as nitrate. Three days after injection, the amounts of uranium in the kidneys represented 2.6 μg of DU g -1 of tissue, considered as a sub-nephrotoxic dosage. The central effect of uranium could be seen through a decrease in food intake as early as the first day after exposure and shorter paradoxical sleep 3 days after acute DU exposure (-18% of controls). With a lower dosage of DU (70 ± 8 μg DU kg -1 ), no significant effect was observed on the sleep-wake cycle. The present study intends to illustrate the fact that the brain is a target organ, as are the kidneys, after acute exposure to a moderate dosage of DU. The mechanisms by which uranium causes these early neurophysiological perturbations shall be discussed

Final programmatic environmental impact statement for alternative strategies for the long-term management and use of depleted uranium hexafluoride. Volume 1: Main text

International Nuclear Information System (INIS)

1999-04-01

This PEIS assesses the potential impacts of alternative management strategies for depleted uranium hexafluoride (UF 6 ) currently stored at three DOE sites: Paducah site near Paducah, Kentucky, Portsmouth site near Portsmouth, Ohio; and K-25 site on the Oak Ridge Reservation, Oak Ridge, Tennessee. The alternatives analyzed in the PEIS include no action, long-term storage as UF 6 , long-term storage as uranium oxide, use as uranium oxide, use as uranium metal, and disposal. DOE's preferred alternative is to begin conversion of the depleted UF 6 inventory as soon as possible, either to uranium oxide, uranium metal, or a combination of both, while allowing for use of as much of this inventory as possible

Incentives for the use of depleted uranium alloys as transport cask containment structure

International Nuclear Information System (INIS)

McConnell, P.; Salzbrenner, R.; Wellman, G.W.; Sorenson, K.B.

1993-01-01

Radioactive material transport casks use either lead or depleted uranium (DU) as gamma-ray shielding material. Stainless steel is conventionally used for structural containment. If a DU alloy had sufficient properties to guarantee resistance to failure during both normal use and accident conditions to serve the dual-role of shielding and containment, the use of other structural materials (i.e., stainless steel) could be reduced. (It is recognized that lead can play no structural role.) Significant reductions in cask weight and dimensions could then be achieved perhaps allowing an increase in payload. The mechanical response of depleted uranium has previously not been included in calculations intended to show that DU-shielded transport casks will maintain their containment function during all conditions. This paper describes a two-part study of depleted uranium alloys: First, the mechanical behavior of DU alloys was determined in order to extend the limited set of mechanical properties reported in the literature (Eckelmeyer, 1991). The mechanical properties measured include the tensile behavior the impact energy. Fracture toughness testing was also performed to determine the sensitivity of DU alloys to brittle fracture. Fracture toughness is the inherent material property which quantifies the fracture resistance of a material. Tensile strength and ductility are significant in terms of other failure modes, however, as will be discussed. These mechanical properties were then input into finite element calculations of cask response to loading conditions to quantify the potential for claiming structural credit for DU. (The term 'structural credit' describes whether a material has adequate properties to allow it to assume a positive role in withstanding structural loadings.) (J.P.N.)

The Absorption-Desorption of Hydrogen by 1.5 g Depleted Uranium

Energy Technology Data Exchange (ETDEWEB)

Kim, Sunmi; Paek, Seungwoo; Lee, Minsoo; Kim, Si-Hyung; Kim, Kwang-Rag; Ahn, Do-Hee [Korea Atomic Energy Research Institute, Daejeon (Korea, Republic of); Sohn, Soon Hwan; Song, Kyu Min [Korea Electric Power Research Institute, Daejeon (Korea, Republic of)

2008-10-15

The form of metal tritides is one of the most popular methods for the storage of hydrogen isotopes. Particularly when metal is in a powder form, the storage capacity of hydrogen isotopes become the maximum value. Here, a 1.5g depleted uranium metal was decrepitated into a powder upon an absorption and desorption of hydrogen gas. The conditions for an activation, absorption-desorption of the hydrogen were defined.

The Absorption-Desorption of Hydrogen by 1.5 g Depleted Uranium

International Nuclear Information System (INIS)

Kim, Sunmi; Paek, Seungwoo; Lee, Minsoo; Kim, Si-Hyung; Kim, Kwang-Rag; Ahn, Do-Hee; Sohn, Soon Hwan; Song, Kyu Min

2008-01-01

The form of metal tritides is one of the most popular methods for the storage of hydrogen isotopes. Particularly when metal is in a powder form, the storage capacity of hydrogen isotopes become the maximum value. Here, a 1.5g depleted uranium metal was decrepitated into a powder upon an absorption and desorption of hydrogen gas. The conditions for an activation, absorption-desorption of the hydrogen were defined

Biological effects of embedded depleted uranium (DU). Summary of Armed Forces Radiobiology Research Institute research

International Nuclear Information System (INIS)

McClain, D.E.; Dalton, T.K.; Emond, C.A.; Hodge, S.J.; Kalinich, J.F.; Landauer, M.A.; Miller, A.C.; Stewart, M.D.; Villa, V.; Xu, J.; Benson, K.A.; Ejnik, J.; Pellmar, T.C.

2001-01-01

The Persian Gulf War resulted in injuries of US Coalition personnel by fragments of depleted uranium (DU). Fragments not immediately threatening the health of the individuals were allowed to remain in place, based on long-standing treatment protocols designed for other kinds of metal shrapnel injuries. However, questions were soon raised as to whether this approach is appropriate for a metal with the unique radiological and toxicological properties of DU. The Armed Forces Radiobiology Research Institute (AFRRI) is investigating health effects of embedded fragments of DU to determine whether current surgical fragment removal policies remain appropriate for this metal. These studies employ rodents implanted with DU pellets as well as cultured human cells exposed to DU compounds. Results indicate uranium from implanted DU fragments distributed to tissues far-removed from implantation sites, including bone, kidney, muscle, and liver. Despite levels of uranium in the kidney that were nephrotoxic after acute exposure, no histological or functional kidney toxicity was observed. However, results suggest the need for further studies of long-term health impact, since DU was found to be mutagenic, and it transformed human osteoblast cells to a tumorigenic phenotype. It also altered neurophysiological parameters in rat hippocampus, crossed the placental barrier, and entered fetal tissue. This report summarizes AFRRI's depleted uranium research to date

Steady State Sputtering Yields and Surface Compositions of Depleted Uranium and Uranium Carbide bombarded by 30 keV Gallium or 16 keV Cesium Ions.

Energy Technology Data Exchange (ETDEWEB)

Siekhaus, W. J. [Lawrence Livermore National Lab. (LLNL), Livermore, CA (United States); Teslich, N. E. [Lawrence Livermore National Lab. (LLNL), Livermore, CA (United States); Weber, P. K. [Lawrence Livermore National Lab. (LLNL), Livermore, CA (United States)

2014-10-23

Depleted uranium that included carbide inclusions was sputtered with 30-keV gallium ions or 16-kev cesium ions to depths much greater than the ions’ range, i.e. using steady-state sputtering. The recession of both the uranium’s and uranium carbide’s surfaces and the ion corresponding fluences were used to determine the steady-state target sputtering yields of both uranium and uranium carbide, i.e. 6.3 atoms of uranium and 2.4 units of uranium carbide eroded per gallium ion, and 9.9 uranium atoms and 3.65 units of uranium carbide eroded by cesium ions. The steady state surface composition resulting from the simultaneous gallium or cesium implantation and sputter-erosion of uranium and uranium carbide were calculated to be U₈₆Ga₁₄, (UC)₇₀Ga₃₀ and U₈₁Cs₉, (UC)₇₉Cs₂₁, respectively.

Depleted uranium storage and disposal trade study: Summary report

Energy Technology Data Exchange (ETDEWEB)

Hightower, J.R.; Trabalka, J.R.

2000-02-01

The objectives of this study were to: identify the most desirable forms for conversion of depleted uranium hexafluoride (DUF6) for extended storage, identify the most desirable forms for conversion of DUF6 for disposal, evaluate the comparative costs for extended storage or disposal of the various forms, review benefits of the proposed plasma conversion process, estimate simplified life-cycle costs (LCCs) for five scenarios that entail either disposal or beneficial reuse, and determine whether an overall optimal form for conversion of DUF6 can be selected given current uncertainty about the endpoints (specific disposal site/technology or reuse options).

Depleted uranium storage and disposal trade study: Summary report

International Nuclear Information System (INIS)

Hightower, J.R.; Trabalka, J.R.

2000-01-01

The objectives of this study were to: identify the most desirable forms for conversion of depleted uranium hexafluoride (DUF6) for extended storage, identify the most desirable forms for conversion of DUF6 for disposal, evaluate the comparative costs for extended storage or disposal of the various forms, review benefits of the proposed plasma conversion process, estimate simplified life-cycle costs (LCCs) for five scenarios that entail either disposal or beneficial reuse, and determine whether an overall optimal form for conversion of DUF6 can be selected given current uncertainty about the endpoints (specific disposal site/technology or reuse options)

Exposure to depleted uranium does not alter the co-expression of HER-2/neu and p53 in breast cancer patients

Directory of Open Access Journals (Sweden)

Al-Toriahi Kaswer M

2011-03-01

Full Text Available Abstract Background Amongst the extensive literature on immunohistochemical profile of breast cancer, very little is found on populations exposed to a potential risk factor such as depleted uranium. This study looked at the immunohistochemical expression of HER-2/neu (c-erbB2 and p53 in different histological types of breast cancer found in the middle Euphrates region of Iraq, where the population has been exposed to high levels of depleted uranium. Findings The present investigation was performed over a period starting from September 2008 to April 2009. Formalin-fixed, paraffin-embedded blocks from 70 patients with breast cancer (62 ductal and 8 lobular carcinoma were included in this study. A group of 25 patients with fibroadenoma was included as a comparative group, and 20 samples of normal breast tissue sections were used as controls. Labeled streptavidin-biotin (LSAB+ complex method was employed for immunohistochemical detection of HER-2/neu and p53. The detection rate of HER-2/neu and p53 immunohistochemical expression were 47.14% and 35.71% respectively in malignant tumors; expression was negative in the comparative and control groups (p HER-2/neu immunostaining was significantly associated with histological type, tumor size, nodal involvement, and recurrence of breast carcinoma (p p Both biomarkers were positively correlated with each other. Furthermore, all the cases that co-expressed both HER-2/neu and p53 showed the most unfavorable biopathological profile. Conclusion P53 and HER-2/neu over-expression play an important role in pathogenesis of breast carcinoma. The findings indicate that in regions exposed to high levels of depleted uranium, although p53 and HER-2/neu overexpression are both high, correlation of their expression with age, grade, tumor size, recurrence and lymph node involvement is similar to studies that have been conducted on populations not exposed to depleted uranium. HER-2/neu expression in breast cancer was higher

Draft Programmatic Environmental Impact Statement for alternative strategies for the long-term management and use of depleted uranium hexafluoride. Volume 2: Appendices

International Nuclear Information System (INIS)

1997-12-01

This PEIS assesses the potential impacts of alternative management of alternative management strategies for depleted uranium hexafluoride (UF 6 ) currently stored at three DOE sites: Paducah site near Paducah, Kentucky; Portsmouth site near Portsmouth, Ohio; and K-25 site on the Oak Ridge Reservation, Oak Ridge, Tennessee. The alternatives analyzed in the PEIS include no action, long-term storage as UF 6 , long-term storage as uranium oxide, use as uranium oxide, use as uranium metal, and disposal. The preferred alternative for the long-term management of depleted UF 6 is to use the entire inventory of material. This volume contains the appendices to volume I

Uranium compounds in ceramic enamels-radioactivity analysis and use hazards

International Nuclear Information System (INIS)

Cucchi, G.; Amadesi, P.

1980-01-01

An analysis was made of the radioactivity of enamel samples, containing depleted Uranium and Uranium ore, such as employed by the ceramic industry to produce paving and lining tiles. An investigation was also made of various types of tiles with depleted Uranium containing enamels, in order to evaluate the use hazard for dwelling houses, in particular in regard to the wear of tiled floors by children as a critical group. The risk to the population due to the use of tiles dyed with enamel containing depleted Uranium was considered an undue risk and as such not permissible. (U.K.)

Draft Programmatic Environmental Impact Statement for alternative strategies for the long-term management and use of depleted uranium hexafluoride. Volume 1: Main text

International Nuclear Information System (INIS)

1997-12-01

This PEIS assesses the potential impacts of alternative management of alternative management strategies for depleted uranium hexafluoride (UF 6 ) currently stored at three DOE sites: Paducah site near Paducah, Kentucky; Portsmouth site near Portsmouth, Ohio; and K-25 site on the Oak Ridge Reservation, Oak Ridge, Tennessee. The alternatives analyzed in the PEIS include no action, long-term storage as UF 6 , long-term storage as uranium oxide, use as uranium oxide, use as uranium metal, and disposal. The preferred alternative for the long-term management of depleted UF 6 is to use the entire inventory of material

Preliminary study of depleted uranium aerosol migration in soils

International Nuclear Information System (INIS)

Guo Zhiying; Yu Shui; Zheng Yonghong; Liang Yueqin; Liu Liping; Song Zhanjun; Zhao Fa

2007-01-01

Objective: To explore the depth of depleted uranium (DU) migration in six main kinds of Chinese soils and the pollution of the groundwater made by DU migration. Methods: With the circulating column model and the inductively coupled plasma-mass spectrometry (ICP-MS), concentration of uranium and the ratio of 235 U/ 238 U in different depth soils and in the corresponding filter liquids had been determined. Results: In the acid rain of pH 3.0, the migration depth of DU in the washed soil and brown soil were 6-8 cm and 4-6 cm, respectively. And with the increment of the acidity of the acid rain, the migration depth of DU in the soils was increased. The migration depth of DU in the 6 types soils was 0-4 cm. The distributed factor between the liquids and soils was lower than 0.004, and the concentration of uranium in the filter liquids was 0.05-10.33 μg/L. Conclusions: The migration depth of DU in soils can be increased by the acid rain, and the majority of DU was stayed in the upper soils and DU pollution might exist for long time, but the probability of groundwater pollution was low. The migration capability of DU was interrelated with the concentration of organic compound in the soils. (authors)

Separation of Depleted Uranium From Soil

Science.gov (United States)

2009-03-01

only. Total DU disso- lution and precipitation 1, 25-Kg sample DU Garden Excavation samples Intact penetra- tors 5 years Buried at depths that...4.76-mm frac- tion was separated into DU and non-DU-containing fractions. The ura- nium concentration of the >4.76-mm fraction was determined gravimetri ... gravimetri - cally. Each of the size fractions ɜ.76 mm was ground in the field and digested and analyzed in the laboratory. Table 15 presents the uranium

On depleted uranium: gulf war and Balkan syndrome.

Science.gov (United States)

Duraković, A

2001-04-01

The complex clinical symptomatology of chronic illnesses, commonly described as Gulf War Syndrome, remains a poorly understood disease entity with diversified theories of its etiology and pathogenesis. Several causative factors have been postulated, with a particular emphasis on low level chemical warfare agents, oil fires, multiple vaccines, desert sand (Al-Eskan disease), botulism, Aspergillus flavus, Mycoplasma, aflatoxins, and others, contributing to the broad scope of clinical manifestations. Among several hundred thousand veterans deployed in the Operation Desert Storm, 15-20% have reported sick and about 25,000 died. Depleted uranium (DU), a low-level radioactive waste product of the enrichment of natural uranium with U-235 for the reactor fuel or nuclear weapons, has been considered a possible causative agent in the genesis of Gulf War Syndrome. It was used in the Gulf and Balkan wars as an armor-penetrating ammunition. In the operation Desert Storm, over 350 metric tons of DU was used, with an estimate of 3-6 million grams released in the atmosphere. Internal contamination with inhaled DU has been demonstrated by the elevated excretion of uranium isotopes in the urine of the exposed veterans 10 years after the Gulf war and causes concern because of its chemical and radiological toxicity and mutagenic and carcinogenic properties. Polarized views of different interest groups maintain an area of sustained controversy more in the environment of the public media than in the scientific community, partly for the reason of being less than sufficiently addressed by a meaningful objective interdisciplinary research.

A technical study of TLD beta calibration factor for exposures to depleted uranium

International Nuclear Information System (INIS)

Ashley, J.C.; Turner, J.E.; McMahan, K.L.; Souleyrette, M.L.; Bogard, R.S.

1995-06-01

The beta calibration factor for converting light output (on reading a thermoluminescent dosimeter) to shallow dose equivalent has been reexamined through theoretical calculations and experimental measurements. The results support the previously determined value for contact with a depleted uranium slab but indicate that for many actual workplace situations, the contact value may be overly conservative

Determination of isotopic uranium in food and water

International Nuclear Information System (INIS)

Baratta, E.J.; Mackill, P.

2001-01-01

The U.S. Food and Drug Administration (FDA) conducts surveys of foods both domestic and imported for the presence of radioactivity. It does not routinely analyze for the actinides, specifically uranium, as it has been shown by previously by studies as reported by WELFORD and others that the concentration in food is very low. This was the result of a 'Tri-City' study. However, at specific sites, the FDA has been requested to analyze for uranium. The concern is that either 'enriched' or 'depleted' uranium has been introduced into the environment and possibly contaminated the food supply. In addition some concern has been raised that water from wells or other sources used for processing food may contain uranium, both natural, depleted or enriched. Methodology for the determination of isotopic uranium, specifically for uranium-238 (depleted) and/or uranium-235 (enriched) in the analyses of food and water samples and the results of these surveys are discussed. (author)

Determination of 236U and transuranium elements in depleted uranium ammunition by α-spectrometry and ICP-MS

International Nuclear Information System (INIS)

Desideri, D.; Meli, M.A.; Roselli, C.; Testa, C.; Boulyga, S.F.; Becker, J.S.

2002-01-01

It is well known that ammunition containing depleted uranium (DU) was used by NATO during the Balkan conflict. To evaluate the origin of DU (the enrichment of natural uranium or the reprocessing of spent nuclear fuel) it is necessary to directly detect the presence of activation products ( 236 U, 239 Pu, 240 Pu, 241 Am, and 237 Np) in the ammunition. In this work the analysis of actinides by α-spectrometry was compared with that by inductively coupled plasma mass spectrometry (ICP-MS) after selective separation of ultratraces of transuranium elements from the uranium matrix. 242 Pu and 243 Am were added to calculate the chemical yield. Plutonium was separated from uranium by extraction chromatography, using tri-n-octylamine (TNOA), with a decontamination factor higher than 10 6 ; after elution plutonium was determined by ICP-MS ( 239 Pu and 240 Pu) and α-spectrometry ( 239+240 Pu) after electroplating. The concentration of Pu in two DU penetrator samples was 7 x 10 -12 g g -1 and 2 x 10 -11 g g -1 . The 240 Pu/ 239 Pu isotope ratio in one penetrator sample (0.12±0.04) was significantly lower than the 240 Pu/ 239 Pu ratios found in two soil samples from Kosovo (0.35±0.10 and 0.27±0.07). 241 Am was separated by extraction chromatography, using di(2-ethylhexyl)phosphoric acid (HDEHP), with a decontamination factor as high as 10 7 . The concentration of 241 Am in the penetrator samples was 2.7 x 10 -14 g g -1 and -15 g g -1 . In addition 237 Np was detected at ultratrace levels. In general, ICP-MS and α-spectrometry results were in good agreement.The presence of anthropogenic radionuclides ( 236 U, 239 Pu, 240 Pu, 241 Am, and 237 Np) in the penetrators indicates that at least part of the uranium originated from the reprocessing of nuclear fuel. Because the concentrations of radionuclides are very low, their radiotoxicological effect is negligible. (orig.)

Determination of (236)U and transuranium elements in depleted uranium ammunition by alpha-spectrometry and ICP-MS.

Science.gov (United States)

Desideri, D; Meli, M A; Roselli, C; Testa, C; Boulyga, S F; Becker, J S

2002-11-01

It is well known that ammunition containing depleted uranium (DU) was used by NATO during the Balkan conflict. To evaluate the origin of DU (the enrichment of natural uranium or the reprocessing of spent nuclear fuel) it is necessary to directly detect the presence of activation products ((236)U, (239)Pu, (240)Pu, (241)Am, and (237)Np) in the ammunition. In this work the analysis of actinides by alpha-spectrometry was compared with that by inductively coupled plasma mass spectrometry (ICP-MS) after selective separation of ultratraces of transuranium elements from the uranium matrix. (242)Pu and (243)Am were added to calculate the chemical yield. Plutonium was separated from uranium by extraction chromatography, using tri- n-octylamine (TNOA), with a decontamination factor higher than 10(6); after elution plutonium was determined by ICP-MS ((239)Pu and (240)Pu) and alpha-spectrometry ((239+240)Pu) after electroplating. The concentration of Pu in two DU penetrator samples was 7 x 10(-12) g g(-1) and 2 x 10(-11) g g(-1). The (240)Pu/(239)Pu isotope ratio in one penetrator sample (0.12+/-0.04) was significantly lower than the (240)Pu/(239)Pu ratios found in two soil samples from Kosovo (0.35+/-0.10 and 0.27+/-0.07). (241)Am was separated by extraction chromatography, using di(2-ethylhexyl)phosphoric acid (HDEHP), with a decontamination factor as high as 10(7). The concentration of (241)Am in the penetrator samples was 2.7 x 10(-14) g g(-1) and <9.4 x 10(-15) g g(-1). In addition (237)Np was detected at ultratrace levels. In general, ICP-MS and alpha-spectrometry results were in good agreement. The presence of anthropogenic radionuclides ((236)U, (239)Pu,(240)Pu, (241)Am, and (237)Np) in the penetrators indicates that at least part of the uranium originated from the reprocessing of nuclear fuel. Because the concentrations of radionuclides are very low, their radiotoxicological effect is negligible.

Remediation of soils contaminated with particulate depleted uranium by multi stage chemical extraction

Energy Technology Data Exchange (ETDEWEB)

Crean, Daniel E. [Immobilisation Science Laboratory, Department of Materials Science and Engineering, The University of Sheffield (United Kingdom); Centre for Radiochemistry Research, School of Chemistry, The University of Manchester (United Kingdom); Livens, Francis R.; Sajih, Mustafa [Centre for Radiochemistry Research, School of Chemistry, The University of Manchester (United Kingdom); Stennett, Martin C. [Immobilisation Science Laboratory, Department of Materials Science and Engineering, The University of Sheffield (United Kingdom); Grolimund, Daniel; Borca, Camelia N. [Swiss Light Source, Paul Scherrer Institute, Villigen (Switzerland); Hyatt, Neil C., E-mail: n.c.hyatt@sheffield.ac.uk [Immobilisation Science Laboratory, Department of Materials Science and Engineering, The University of Sheffield (United Kingdom)

2013-12-15

Highlights: • Batch leaching was examined to remediate soils contaminated with munitions depleted uranium. • Site specific maximum extraction was 42–50% total U in single batch with NH{sub 4}HCO{sub 3}. • Analysis of residues revealed partial leaching and secondary carbonate phases. • Sequential batch leaching alternating between NH{sub 4}HCO{sub 3} and citric acid was designed. • Site specific extraction was increased to 68–87% total U in three batch steps. -- Abstract: Contamination of soils with depleted uranium (DU) from munitions firing occurs in conflict zones and at test firing sites. This study reports the development of a chemical extraction methodology for remediation of soils contaminated with particulate DU. Uranium phases in soils from two sites at a UK firing range, MOD Eskmeals, were characterised by electron microscopy and sequential extraction. Uranium rich particles with characteristic spherical morphologies were observed in soils, consistent with other instances of DU munitions contamination. Batch extraction efficiencies for aqueous ammonium bicarbonate (42–50% total DU extracted), citric acid (30–42% total DU) and sulphuric acid (13–19% total DU) were evaluated. Characterisation of residues from bicarbonate-treated soils by synchrotron microfocus X-ray diffraction and X-ray absorption spectroscopy revealed partially leached U(IV)-oxide particles and some secondary uranyl-carbonate phases. Based on these data, a multi-stage extraction scheme was developed utilising leaching in ammonium bicarbonate followed by citric acid to dissolve secondary carbonate species. Site specific U extraction was improved to 68–87% total U by the application of this methodology, potentially providing a route to efficient DU decontamination using low cost, environmentally compatible reagents.

Morphology study on the depleted uranium as hydriding/dehydriding cycles

Energy Technology Data Exchange (ETDEWEB)

Chung, Dong-you, E-mail: dongyou@nfri.re.kr [National Fusion Research Institute, Daejeon (Korea, Republic of); Yun, Sei-Hun; Kang, Hyun-Goo; Chang, Min Ho; Oh, Yun Hee [National Fusion Research Institute, Daejeon (Korea, Republic of); Kang, Kweon Ho; Woo, Yoon Myung [Korea Atomic Energy Research Institute, Daejeon (Korea, Republic of)

2016-11-01

Depleted Uranium (DU) is one of the strongest candidates as a getter material of hydrogen isotopes in the nuclear fusion reactor. In this work, small DU lump specimen with 99.8% purity was prepared for observation of morphology variation as hydriding/dehydriding cycles. Hydriding/dehydriding of DU was carried out more than 10 cycles for powder preparation. The pulverized DU specimen was safely handled in the glove box under Argon gas condition to minimize contact with oxygen and humidity. The morphology change according to hydriding/dehydriding cycles was observed by visual cell reactor, optical microscope and scanning electron microscope. The first hydriding of the small DU sample has progressed slowly with surface enlargement and volume expansion as time passes. After third hydriding/dehydriding cycles, most of DU was pulverized. The powder fineness of DU developed as hydriding/dehydriding cycle progresses. But the agglomerates of fine DU particles were observed. It was confirmed that the DU particles exist as porous agglomerates. And the particle agglomerate shows poor fluidity and even has the cohesive force.

Contamination with radionuclides and depleted uranium as a result of NATO aggression against Yugoslavia

International Nuclear Information System (INIS)

Veselinovic, D.; Kopecni, M.M.

2001-01-01

It appears that the amount of depleted uranium (DU) is approaching 10 6 tons at world level. Depleted uranium is a by-product in uranium enrichment process. As such, and at the same time being low radioactive, DU has legal status of low-level radioactive waste. On the other hand, DU is natural present in nature. This is the reason why many claim that it cannot produce major damage if discharged in the environment and that it can be used for ammunition construction material. To regret, DU due to its remarkable physical and mechanical properties has been widely used for the military purposes only. Nowadays many armies have it as a part of standard ammunition stock. To much less extend, it has been used as a shield for various types of armored vehicles. So far, DU has been extensively used on a large scale at several locations on the globe. The most important ones are the test area in Mohave Desert, USA, Gulf War, Iraq, Bosnia and Herzegovina and most recently NATO aggression on Yugoslavia. As a result of extensive DU use, there are many pro and contras regarding DU harmful effects on the environment and life in general. On the subject expert opinion strongly disagree, while public opinion is very much against its use, in particular for military purpose.From the existing experience on the DU impact on the life and environment it is evident that DU can create harmful effects. So far, humans were of prime importance and most of the observations, results and discussions refer to humans, but also there is a growing concern for the biota in general. This paper summarizes some of the known facts regarding depleted uranium, its use as a material for ammunition manufacturing and possible harmful affects in connection with it. Paper also suggests some of the measures that could be considered to follow and remedy the current DU contamination of Kosovo and Metohija, and some other spots in FR Yugoslavia. (author)

Natural and depleted uranium in the topsoil of Qatar: Is it something to worry about?

International Nuclear Information System (INIS)

Shomar, Basem; Amr, Mohamed; Al-Saad, Khalid; Mohieldeen, Yasir

2013-01-01

Highlights: • Scientific studies on Uranium in the arid environment are almost absent. • Qatar is closed to Iraq and Iran where the two countries were exposed to long wars. • The paper introduces baseline study integrates chemistry, instrumentation and GIS mapping. • The study opens new horizons for similar studies on the field using similar approach. - Abstract: This study examines uranium in soils of Qatar to investigate whether there is any detectable traces of depleted uranium (DU). 409 soil samples were collected using a 10 km grid system throughout the State of Qatar. The U concentrations and isotopic compositions ( 235 U/ 238 U) were determined using an ICP-MS. The U concentrations range from 0.05 to 4.7 mg/kg and the 235 U/ 238 U isotopic signatures are in the range 0.007–0.008, i.e. comparable to the isotopic ratio in natural uranium (NU). The distribution of these concentrations in the topsoil were used to see correlations with locations of pollution point sources and environmentally hot areas associated with human activity: industrial estates, solid waste dumping sites, wastewater treatment plants, sea harbors, airports, and public transport network. New thematic maps were built using Geographic Information System (GIS) software. The results showed that there is no linkage between the occurrence, distribution, concentrations and isotopic ratios of U and these hotspots. More importantly, due to the low concentration of organic matter (OM) in soils of Qatar, very limited P-fertilization, the alkaline nature of soil (pH 8) and low Fe/Mn contents make soil uranium concentrations very low. The residential areas, including the capital Doha, had the lowest total concentrations of uranium and isotopic ratios of the country while the northern and western parts showed the highest values

Decommissioning plan depleted uranium manufacturing facility

International Nuclear Information System (INIS)

Bernhardt, D.E.; Pittman, J.D.; Prewett, S.V.

1987-01-01

Aerojet Ordnance Tennessee, Inc. (Aerojet) is decommissioning its California depleted uranium (DU) manufacturing facility. Aerojet has conducted manufacturing and research and development activities at the facility since 1977 under a State of California Source Materials License. The decontamination is being performed by a contractor selector for technical competence through competitive bid. Since the facility will be released for uncontrolled use it will be decontaminated to levels as low as reasonably achievable (ALARA). In order to fully apply the principles of ALARA, and ensure the decontamination is in full compliance with appropriate guides, Aerojet has retained Rogers and Associaties Engineering Corporation (RAE) to assist in the decommissioning. RAE has assisted in characterizing the facility and preparing contract bid documents and technical specifications to obtain a qualified decontamination contractor. RAE will monitor the decontamination work effort to assure the contractor's performance complies with the contract specifications and the decontamination plan. The specifications require a thorough cleaning and decontamination of the facility, not just sufficient cleaning to meet the numeric cleanup criteria

Uranium tipped ammunition

International Nuclear Information System (INIS)

Roche, P.

1993-01-01

During the uranium enrichment process required to make nuclear weapons or fuel, the concentration of the 'fissile' U-235 isotope has to be increased. What is left, depleted uranium, is about half as radioactive as natural uranium, but very dense and extremely hard. It is used in armour piercing shells. External radiation levels from depleted uranium (DU) are low. However DU is about as toxic as lead and could be harmful to the kidneys if eaten or inhaled. It is estimated that between 40 and 300 tonnes of depleted uranium were left behind by the Allied armies after the Gulf war. The biggest hazard would be from depleted uranium shells which have hit Iraqui armoured vehicles and the resulting dust inhaled. There is a possible link between depleted uranium shells and an illness known as 'Desert Storm Syndrome' occurring in some Gulf war veterans. As these shells are a toxic and radioactive hazard to health and the environment their use and testing should be stopped because of the risks to troops and those living near test firing ranges. (UK)

The state of knowledge about the potential risks associated to depleted uranium used in weapons; Etat des connaissances sur les risques potentiels associes a l'uranium appauvri utilise dans les armes

Energy Technology Data Exchange (ETDEWEB)

NONE

2001-01-01

This document brigs back the actual knowledge on uranium and its chemical and radiological toxicity. It pays particular attention to discuss the elements allowing to assess the risks linked to the man exposure to depleted uranium. (N.C.)

Radiological chronometry of uranium metal samples

International Nuclear Information System (INIS)

Meyers, L.A.; Stalcup, A.M.; Glover, S.E.; Spitz, H.B.; LaMont, S.P.

2014-01-01

Radiological chronometry is an important tool in nuclear forensics that uses several methods to determine the length of time that has elapsed since a material was last purified. One of the chronometers used in determining the age of metallic uranium involves measuring the fractional ingrowth of 230 Th from its parent 234 U with the assumption that the uranium metal contained no impurities, especially thorium, when it was purified. The affects of different etching procedures were evaluated for the removal of surface oxidation with three different types of uranium metal samples to determine whether the etching procedure affects the radiological age. The sample treated with a rigorous etching procedure had exhibited the most reliable radiological age while less rigorous etching yields a radiological age from 15 years to hundreds of years older than the known age. Any excess thorium on the surface of a uranium metal sample presents a bias in age determination and the sample will appear older than the true age. Although this research demonstrates the need for rigorous surface etching, a bias in the radiological age could have arisen if the uranium in the metal was heterogeneously distributed. (author)

Phyto remediation of Depleted Uranium from Contaminated Soil and Sediments

International Nuclear Information System (INIS)

Al-Saad, K.A.; Amr, M.A.

2012-01-01

Seedlings of sunflower (Helianthus annuus L.) was used to test the effect of ph, citric acid, phosphoric acid, and ethylene-diamine-tetraacetic acid (EDTA) on the uptake and the translocation of depleted uranium (DU). The experiments was performed in hydroponic cultures and environmental soil samples collected from Qatar. The results of hydroponic experiment indicated that DU accumulated more in the roots than leaves, in the plants that was grown in contaminated water. The presence of phosphoric acid, citric acid, or EDTA showed different patterns of DU uptake. Higher transfer factor was observed when phosphoric acid was added. When EDTA was added, higher DU uptake was observed. The data suggested the DU was mostly retained to the root when EDTA was added. Also, the experiments were applied on environmental soil samples collected from Qatar. The presence of phosphoric acid, citric acid, or EDTA showed different patterns of DU uptake for the three different soil samples. The addition of EDTA increased the DU uptake in the sunflowers planted in the three types of soils. The results indicated that, generally, DU accumulated more in the roots compared to leaves and stems, except when soil was spiked with phosphoric acid. The translocation ratio was limited but highest ( 1.4) in the sunflower planted in soil S2705 when spiked with phosphoric acid. In the three soils tested, the result suggested higher DU translocation of sunflower with the presence of phosphoric acid.

Depleted uranium oxides as spent-nuclear-fuel waste-package invert and backfill materials

International Nuclear Information System (INIS)

Forsberg, C.W.; Haire, M.J.

1997-01-01

A new technology has been proposed in which depleted uranium, in the form of oxides or silicates, is placed around the outside of the spent nuclear fuel waste packages in the geological repository. This concept may (1) reduce the potential for repository nuclear criticality events and (2) reduce long-term release of radionuclides from the repository. As a new concept, there are significant uncertainties

Solubility of airborne uranium samples from uranium processing plant

International Nuclear Information System (INIS)

Kravchik, T.; Oved, S.; Sarah, R.; Gonen, R.; Paz-Tal, O.; Pelled, O.; German, U.; Tshuva, A.

2005-01-01

Full text: During the production and machining processes of uranium metal, aerosols might be released to the air. Inhalation of these aerosols is the main route of internal exposure of workers. To assess the radiation dose from the intake of these uranium compounds it is necessary to know their absorption type, based on their dissolution rate in extracellular aqueous environment of lung fluid. The International Commission on Radiological Protection (ICRP) has assigned UF4 and U03 to absorption type M (blood absorption which contains a 10 % fraction with an absorption rate of 10 minutes and 90 % fraction with an absorption rate of 140 fays) and UO2 and U3O8 to absorption type S (blood absorption rate with a half-time of 7000 days) in the ICRP-66 model.The solubility classification of uranium compounds defined by the ICRP can serve as a general guidance. At specific workplaces, differences can be encountered, because of differences in compounds production process and the presence of additional compounds, with different solubility characteristics. According to ICRP recommendations, material-specific rates of absorption should be preferred to default parameters whenever specific experimental data exists. Solubility profiles of uranium aerosols were determined by performing in vitro chemical solubility tests on air samples taken from uranium production and machining facilities. The dissolution rate was determined over 100 days in a simultant solution of the extracellular airway lining fluid. The filter sample was immersed in a test vial holding 60 ml of simultant fluid, which was maintained at a 37 o C inside a thermostatic bath and at a physiological pH of 7.2-7.6. The test vials with the solution were shaken to simulate the conditions inside the extracellular aqueous environment of the lung as much as possible. The tests indicated that the uranium aerosols samples taken from the metal production and machining facilities at the Nuclear Research Center Negev (NRCN

The state of knowledge about the potential risks associated to depleted uranium used in weapons; Etat des connaissances sur les risques potentiels associes a l'uranium appauvri utilise dans les armes

Energy Technology Data Exchange (ETDEWEB)

NONE

2001-01-01

This document brigs back the actual knowledge on uranium and its chemical and radiological toxicity. It pays particular attention to discuss the elements allowing to assess the risks linked to the man exposure to depleted uranium. (N.C.)

UNEP and IAEA exploring the possibility of sending depleted uranium missions to Bosnia-Herzegovina, the Federal Republic of Yugoslavia and Iraq

International Nuclear Information System (INIS)

2001-01-01

Full text: Vienna/Nairobi - Mohamed ElBaradei, the Director-General of the International Atomic Energy Agency (IAEA) and Klaus Toepfer, Executive Director of the United Nations Environment Programme (UNEP), have agreed to consider ways and means to respond to requests for fact-finding missions to Bosnia-Herzegovina, the Federal Republic of Yugoslavia and Iraq where depleted uranium (DU) was used during military conflicts. The two organizations will co-ordinate their action with the World Health Organization, which has recently decided to send a team to study the health effects of depleted uranium in Iraq, as well as with other relevant UN system organizations. Pekka Haavisto, Chairman of UNEP's Depleted Uranium Assessment Team, is meeting today with UN officials in Sarajevo for consultations on a possible future mission to Bosnia-Herzegovina. Mr. Haavisto will visit Belgrade tomorrow to meet with officials of the Federal Republic of Yugoslavia. The IAEA is considering holding a training course to improve the understanding and skills of specialist staff from concerned countries. The main focus will be on measurement methods and the assessment of risks from depleted uranium and other radioactivity. The possibility of sending fact-finding missions to Bosnia-Herzegovina, the Federal Republic of Yugoslavia and Iraq follows last year's mission to Kosovo by the UNEP-led DU Assessment Team. UNEP will wait for the scientific findings of the report of the Kosovo mission, expected to be released in early March, before it embarks on new DU field assessments. (author)

Gravimetric determination of uranium in SALE samples

International Nuclear Information System (INIS)

Anon.

1981-01-01

As a participant in the Safeguards Analytical Laboratory Evaluation (SALE) program, the Analytical Chemistry Laboratory at General Atomic routinely assays uranium dioxide and uranyl nitrate SALE samples for uranium content. Gravimetric methods are relatively easy and inexpensive to apply when the samples for uranium content. Gravimetric methods are relatively easy and inexpensive to apply when the samples are free from substantial amounts of metallic impurities. Clearly the gravimetric procedure alone is not specific for uranium and must be enhanced by the use of impurity corrections. Emission spectrography is used routinely as the technique of choice for making such corrections. In cases where it is essential to assay specifically for uranium, the modified Davies-Gray titration using a weighed titrant method is applied. In this paper some essential features of these gravimetric and titrimetric procedures are discussed

Depleted Uranium and Human Health.

Science.gov (United States)

Faa, Armando; Gerosa, Clara; Fanni, Daniela; Floris, Giuseppe; Eyken, Peter V; Lachowicz, Joanna I; Nurchi, Valeria M

2018-01-01

Depleted uranium (DU) is generally considered an emerging pollutant, first extensively introduced into environment in the early nineties in Iraq, during the military operation called "Desert Storm". DU has been hypothesized to represent a hazardous element both for soldiers exposed as well as for the inhabitants of the polluted areas in the war zones. In this review, the possible consequences on human health of DU released in the environment are critically analyzed. In the first part, the chemical properties of DU and the principal civil and military uses are summarized. A concise analysis of the mechanisms underlying absorption, blood transport, tissue distribution and excretion of DU in the human body is the subject of the second part of this article. The following sections deal with pathological condition putatively associated with overexposure to DU. Developmental and birth defects, the Persian Gulf syndrome, and kidney diseases that have been associated to DU are the arguments treated in the third section. Finally, data regarding DU exposure and cancer insurgence will be critically analyzed, including leukemia/lymphoma, lung cancer, uterine cervix cancer, breast cancer, bladder cancer and testicular cancer. The aim of the authors is to give a contribution to the debate on DU and its effects on human health and disease. Copyright© Bentham Science Publishers; For any queries, please email at epub@benthamscience.org.

Physicochemical characterization of Capstone depleted uranium aerosols IV: in vitro solubility analysis.

Science.gov (United States)

Guilmette, Raymond A; Cheng, Yung Sung

2009-03-01

As part of the Capstone Depleted Uranium (DU) Aerosol Study, the solubility of selected aerosol samples was measured using an accepted in vitro dissolution test system. This static system was employed along with a SUF (synthetic ultrafiltrate) solvent, which is designed to mimic the physiological chemistry of extracellular fluid. Using sequentially obtained solvent samples, the dissolution behavior over a 46-d test period was evaluated by fitting the measurement data to two- or three-component negative exponential functions. These functions were then compared with Type M and S absorption taken from the International Commission on Radiological Protection Publication 66 Human Respiratory Tract Model. The results indicated that there was a substantial variability in solubility of the aerosols, which in part depended on the type of armor being impacted by the DU penetrator and the particle size fraction being tested. Although some trends were suggested, the variability noted leads to uncertainties in predicting the solubility of other DU-based aerosols. Nevertheless, these data provide a useful experimental basis for modeling the intake-dose relationships for inhaled DU aerosols arising from penetrator impact on armored vehicles.

Precise Monitoring of Depleted Uranium in human and environment of South Iraq using Multi-collector ICP-MS

International Nuclear Information System (INIS)

Gerdes, A.; Weyer, S.; Brey, G.; Zimmermann, I.; Durakovic, A.

2004-01-01

Multi-collector Inductive Coupled Plasma Mass Spectrometry (MC-ICPMS) becomes increasingly important in monitoring environmental contamination, because it allows detection of long-lived radionuclides at ultra trace levels. High sample throughout combined with high precision and accuracy, low detection limits for most elements and simultaneous detection of up to 9 isotopes makes it prior to most other techniques. For homogeneous samples concentration and isotope composition can be determined with a precision and uncertainty of usually better than 0.5 % using the isotope dilution method, e.g. isotope measurements relative to a well characterized 233 U tracer. Exposure to low-level radioactive dust released into the environment accidentally or by the use of Depleted Uranium (DU) munitions in the military theatre demands precise screening of humans and local environment. Sensitive methods are also needed for monitoring and understanding the pathway of radionuclides in the biosphere and the human body. Using a method recently developed at our department it is for instance possible to detect urinary excretion of DU in the low fg/ml range or at fractions below 0.2% of the total urinary uranium concentration. This allows monitoring the inhalation of up to a few micrograms of insoluble non-natural uranium particles in the lung several months or even years later. As example we will show and discuss results from our study of the uranium isotope composition and concentration of surface water, topsoil and dust from different sites of Baghdad, Basra, and the Suweirah farming area. We also analyzed urine from people living in these areas or stayed their for a relative short time. The samples, also including highly contaminated ones, such as wipes of tank top debris and penetrator channels, were collected from the Uranium Medical Research Centre field team after coalition operation Iraqi Freedom in early October 2003. Total soil samples, separated soil fine-fractions ( 233 U

Depleted uranium in Serbia and Montenegro. Post-conflict environmental assessment in the Federal Republic of Yugoslavia

International Nuclear Information System (INIS)

2002-01-01

This report by the United Nations Environment Programme (UNEP) on the environmental impacts of depleted uranium (DU) is a direct follow-up to last year's report, Depleted Uranium in Kosovo - A Post-Conflict Assessment (2001), and once more brings additional scientific information on DU. This second phase has now been carried out in Serbia and Montenegro, starting with a field mission in October 2001 to collect samples, followed by laboratory work during the winter and the early spring. Our new study provides additional information and reveals important new discoveries on the environmental behaviour of DU. We learn that still, more than two years after the end of the conflict, particles of DU dust can be detected from soil samples and from sensitive bioindicators like lichen. However, as the levels were extremely low, it was only through the use of state-of-the-art laboratory analyses that detection could be achieved. Based on our findings, UNEP can confirm that contamination at the targeted sites is widespread, though no significant level of radioactivity can be measured. Furthermore, during this assessment the UNEP team used modern air sampling techniques and detected airborne DU particles at two sites. While all levels detected are still below international safety limits, these results add valuable new information to the scientific body of knowledge concerning the behaviour of DU and have important implications for site decontamination and construction works. During the mission to Serbia and Montenegro, a serious health concern potentially related to DU was presented to UNEP. This information was forwarded to WHO, as the competent United Nations agency on health issues. The original claim and the formal WHO response are included in this report. Based on our findings, our recommendations remain the same as those we outlined in the previous Kosovo DU study. Future monitoring is clearly needed, as well as awareness-raising for the local population. Clean-up and

Precise Monitoring of Depleted Uranium in human and environment of South Iraq using Multi-collector ICP-MS

Energy Technology Data Exchange (ETDEWEB)

Gerdes, A.; Weyer, S.; Brey, G. [Frankfurt Univ., Dept. of Mineralogy (Germany); Zimmermann, I.; Durakovic, A. [Uranium Medical Research Centre, Toronto (Italy)

2004-07-01

Multi-collector Inductive Coupled Plasma Mass Spectrometry (MC-ICPMS) becomes increasingly important in monitoring environmental contamination, because it allows detection of long-lived radionuclides at ultra trace levels. High sample throughout combined with high precision and accuracy, low detection limits for most elements and simultaneous detection of up to 9 isotopes makes it prior to most other techniques. For homogeneous samples concentration and isotope composition can be determined with a precision and uncertainty of usually better than 0.5 % using the isotope dilution method, e.g. isotope measurements relative to a well characterized {sup 233}U tracer. Exposure to low-level radioactive dust released into the environment accidentally or by the use of Depleted Uranium (DU) munitions in the military theatre demands precise screening of humans and local environment. Sensitive methods are also needed for monitoring and understanding the pathway of radionuclides in the biosphere and the human body. Using a method recently developed at our department it is for instance possible to detect urinary excretion of DU in the low fg/ml range or at fractions below 0.2% of the total urinary uranium concentration. This allows monitoring the inhalation of up to a few micrograms of insoluble non-natural uranium particles in the lung several months or even years later. As example we will show and discuss results from our study of the uranium isotope composition and concentration of surface water, topsoil and dust from different sites of Baghdad, Basra, and the Suweirah farming area. We also analyzed urine from people living in these areas or stayed their for a relative short time. The samples, also including highly contaminated ones, such as wipes of tank top debris and penetrator channels, were collected from the Uranium Medical Research Centre field team after coalition operation Iraqi Freedom in early October 2003. Total soil samples, separated soil fine-fractions (< 100

COGEMA's UMF [Uranium Management Facility

International Nuclear Information System (INIS)

Lamorlette, G.; Bertrand, J.P.

1988-01-01

The French government-owned corporation, COGEMA, is responsible for the nuclear fuel cycle. This paper describes the activities at COGEMA's Pierrelatte facility, especially its Uranium Management Facility. UF6 handling and storage is described for natural, enriched, depleted, and reprocessed uranium. UF6 quality control specifications, sampling, and analysis (halocarbon and volatile fluorides, isotopic analysis, uranium assay, and impurities) are described. In addition, the paper discusses the filling and cleaning of containers and security at UMF

Environmental acceptability of high-performance alternatives for depleted uranium penetrators

Energy Technology Data Exchange (ETDEWEB)

Kerley, C.R.; Easterly, C.E.; Eckerman, K.F. [and others

1996-08-01

The Army`s environmental strategy for investigating material substitution and management is to measure system environmental gains/losses in all phases of the material management life cycle from cradle to grave. This study is the first in a series of new investigations, applying material life cycle concepts, to evaluate whether there are environmental benefits from increasing the use of tungsten as an alternative to depleted uranium (DU) in Kinetic Energy Penetrators (KEPs). Current military armor penetrators use DU and tungsten as base materials. Although DU alloys have provided the highest performance of any high-density alloy deployed against enemy heavy armor, its low-level radioactivity poses a number of environmental risks. These risks include exposures to the military and civilian population from inhalation, ingestion, and injection of particles. Depleted uranium is well known to be chemically toxic (kidney toxicity), and workplace exposure levels are based on its renal toxicity. Waste materials containing DU fragments are classified as low-level radioactive waste and are regulated by the Nuclear Regulatory Commission. These characteristics of DU do not preclude its use in KEPs. However, long-term management challenges associated with KEP deployment and improved public perceptions about environmental risks from military activities might be well served by a serious effort to identify, develop, and substitute alternative materials that meet performance objectives and involve fewer environmental risks. Tungsten, a leading candidate base material for KEPS, is potentially such a material because it is not radioactive. Tungsten is less well studied, however, with respect to health impacts and other environmental risks. The present study is designed to contribute to the understanding of the environmental behavior of tungsten by synthesizing available information that is relevant to its potential use as a penetrator.

Radioactively induced noise in gas-sampling uranium calorimeters

International Nuclear Information System (INIS)

Gordon, H.A.; Rehak, P.

1982-01-01

The signal induced by radioactivity of a U 238 absorber in a cell of a gas-sampling uranium calorimeter was studied. By means of Campbell's theorem, the levels of the radioactively induced noise in uranium gas-sampling calorimeters was calculated. It was shown that in order to obtain similar radioactive noise performance as U-liquid argon or U-scintillator combinations, the α-particles from the uranium must be stopped before entering the sensing volume of gas-uranium calorimeters

Environmental Pollution in five floors (5th to 9th) Resulting from the use of Depleted Uranium Weaponry in the Al-Tahreer Tower Building

International Nuclear Information System (INIS)

Ameen, N.H; Al-ghirrawy, M.A; Kadhim, H.H

2014-01-01

The goals of this study include measuring the increase in radioactivity and removal the contamination regions to protect the population and the environment resulting from bombing the Al-Tahreer Tower Building (the Turkish restaurant previously) by the depleted uranium bullets through direct measurement and sampling of soil from five floors (Fifth,Sixth,Seventh,Eighth,and Ninth) of the building, which contains fourteen floors in addition to basement by using different types of portable monitoring equipment s.The results of radiological surveys by using the portable monitor (CAB) indicated the presence of contaminated soil reached to 55 c/sec, and small particles of depleted uranium shells has very high levels of contamination reached to 70 c /sec ,while the background level is (0.5 c/sec) ,and the higher exposure rates is 55 μR/hr when the portable monitor (Ludlum) put on the contaminated regions approximately on distance 0.5 cm), where the natural background level is 9 μR/hr in the floors of the building.The radiological analyses of the collected soil samples were done in the laboratory of the center of Radiological Researches in the Ministry of sciences and Technology by using gamma spectrometry (which contains High- purity Germanium Detector) with a efficiency of 40% and resolution 2 keV for Energy, 1.33Mev, collection, preparations and tests of soil samples were all done according to IAEA.The laboratory results indicated the presence of high concentrations of the isotopes Th-234 (1550.1) Bq/kg, and Pa-234 m (1394.8) in the soil samples taken from the floors while the concentrations of Th-234 and Pa-234 m in natural background levels are (nearly 40, nil) Bq/Kg respectively which is a clear indication of the presence of high concentrations an isotope of uranium - 238 as they are supposed to be in equilibrium radiation.

Properties, use and health effects of depleted uranium (DU): a general overview

International Nuclear Information System (INIS)

Bleise, A.; Danesi, P.R.; Burkart, W.

2003-01-01

Depleted uranium (DU), a waste product of uranium enrichment, has several civilian and military applications. It was used as armor-piercing ammunition in international military conflicts and was claimed to contribute to health problems, known as the Gulf War Syndrome and recently as the Balkan Syndrome. This led to renewed efforts to assess the environmental consequences and the health impact of the use of DU. The radiological and chemical properties of DU can be compared to those of natural uranium, which is ubiquitously present in soil at a typical concentration of 3 mg/kg. Natural uranium has the same chemotoxicity, but its radiotoxicity is 60% higher. Due to the low specific radioactivity and the dominance of alpha-radiation no acute risk is attributed to external exposure to DU. The major risk is DU dust, generated when DU ammunition hits hard targets. Depending on aerosol speciation, inhalation may lead to a protracted exposure of the lung and other organs. After deposition on the ground, resuspension can take place if the DU containing particle size is sufficiently small. However, transfer to drinking water or locally produced food has little potential to lead to significant exposures to DU. Since poor solubility of uranium compounds and lack of information on speciation precludes the use of radioecological models for exposure assessment, biomonitoring has to be used for assessing exposed persons. Urine, feces, hair and nails record recent exposures to DU. With the exception of crews of military vehicles having been hit by DU penetrators, no body burdens above the range of values for natural uranium have been found. Therefore, observable health effects are not expected and residual cancer risk estimates have to be based on theoretical considerations. They appear to be very minor for all post-conflict situations, i.e. a fraction of those expected from natural radiation

Properties, use and health effects of depleted uranium (DU): a general overview

Energy Technology Data Exchange (ETDEWEB)

Bleise, A.; Danesi, P.R.; Burkart, W. E-mail: w.burkart@iaea.org

2003-07-01

Depleted uranium (DU), a waste product of uranium enrichment, has several civilian and military applications. It was used as armor-piercing ammunition in international military conflicts and was claimed to contribute to health problems, known as the Gulf War Syndrome and recently as the Balkan Syndrome. This led to renewed efforts to assess the environmental consequences and the health impact of the use of DU. The radiological and chemical properties of DU can be compared to those of natural uranium, which is ubiquitously present in soil at a typical concentration of 3 mg/kg. Natural uranium has the same chemotoxicity, but its radiotoxicity is 60% higher. Due to the low specific radioactivity and the dominance of alpha-radiation no acute risk is attributed to external exposure to DU. The major risk is DU dust, generated when DU ammunition hits hard targets. Depending on aerosol speciation, inhalation may lead to a protracted exposure of the lung and other organs. After deposition on the ground, resuspension can take place if the DU containing particle size is sufficiently small. However, transfer to drinking water or locally produced food has little potential to lead to significant exposures to DU. Since poor solubility of uranium compounds and lack of information on speciation precludes the use of radioecological models for exposure assessment, biomonitoring has to be used for assessing exposed persons. Urine, feces, hair and nails record recent exposures to DU. With the exception of crews of military vehicles having been hit by DU penetrators, no body burdens above the range of values for natural uranium have been found. Therefore, observable health effects are not expected and residual cancer risk estimates have to be based on theoretical considerations. They appear to be very minor for all post-conflict situations, i.e. a fraction of those expected from natural radiation.

Properties, use and health effects of depleted uranium (DU): a general overview.

Science.gov (United States)

Bleise, A; Danesi, P R; Burkart, W

2003-01-01

Depleted uranium (DU), a waste product of uranium enrichment, has several civilian and military applications. It was used as armor-piercing ammunition in international military conflicts and was claimed to contribute to health problems, known as the Gulf War Syndrome and recently as the Balkan Syndrome. This led to renewed efforts to assess the environmental consequences and the health impact of the use of DU. The radiological and chemical properties of DU can be compared to those of natural uranium, which is ubiquitously present in soil at a typical concentration of 3 mg/kg. Natural uranium has the same chemotoxicity, but its radiotoxicity is 60% higher. Due to the low specific radioactivity and the dominance of alpha-radiation no acute risk is attributed to external exposure to DU. The major risk is DU dust, generated when DU ammunition hits hard targets. Depending on aerosol speciation, inhalation may lead to a protracted exposure of the lung and other organs. After deposition on the ground, resuspension can take place if the DU containing particle size is sufficiently small. However, transfer to drinking water or locally produced food has little potential to lead to significant exposures to DU. Since poor solubility of uranium compounds and lack of information on speciation precludes the use of radioecological models for exposure assessment, biomonitoring has to be used for assessing exposed persons. Urine, feces, hair and nails record recent exposures to DU. With the exception of crews of military vehicles having been hit by DU penetrators, no body burdens above the range of values for natural uranium have been found. Therefore, observable health effects are not expected and residual cancer risk estimates have to be based on theoretical considerations. They appear to be very minor for all post-conflict situations, i.e. a fraction of those expected from natural radiation.

Determination of {sup 236}U and transuranium elements in depleted uranium ammunition by {alpha}-spectrometry and ICP-MS

Energy Technology Data Exchange (ETDEWEB)

Desideri, D.; Meli, M.A.; Roselli, C.; Testa, C. [General Chemistry Institute, Urbino University, Urbino (Italy); Boulyga, S.F.; Becker, J.S. [Central Department of Analytical Chemistry, Research Centre Juelich, Juelich (Germany)

2002-11-01

It is well known that ammunition containing depleted uranium (DU) was used by NATO during the Balkan conflict. To evaluate the origin of DU (the enrichment of natural uranium or the reprocessing of spent nuclear fuel) it is necessary to directly detect the presence of activation products ({sup 236}U, {sup 239}Pu, {sup 240}Pu, {sup 241}Am, and {sup 237}Np) in the ammunition. In this work the analysis of actinides by {alpha}-spectrometry was compared with that by inductively coupled plasma mass spectrometry (ICP-MS) after selective separation of ultratraces of transuranium elements from the uranium matrix. {sup 242}Pu and {sup 243}Am were added to calculate the chemical yield. Plutonium was separated from uranium by extraction chromatography, using tri-n-octylamine (TNOA), with a decontamination factor higher than 10{sup 6}; after elution plutonium was determined by ICP-MS ({sup 239}Pu and {sup 240}Pu) and {alpha}-spectrometry ({sup 239+240}Pu) after electroplating. The concentration of Pu in two DU penetrator samples was 7 x 10{sup -12} g g{sup -1} and 2 x 10{sup -11} g g{sup -1}. The {sup 240}Pu/{sup 239}Pu isotope ratio in one penetrator sample (0.12{+-}0.04) was significantly lower than the {sup 240}Pu/{sup 239}Pu ratios found in two soil samples from Kosovo (0.35{+-}0.10 and 0.27{+-}0.07). {sup 241}Am was separated by extraction chromatography, using di(2-ethylhexyl)phosphoric acid (HDEHP), with a decontamination factor as high as 10{sup 7}. The concentration of {sup 241}Am in the penetrator samples was 2.7 x 10{sup -14} g g{sup -1} and <9.4 x 10{sup -15} g g{sup -1}. In addition {sup 237}Np was detected at ultratrace levels. In general, ICP-MS and {alpha}-spectrometry results were in good agreement.The presence of anthropogenic radionuclides ({sup 236}U, {sup 239}Pu,{sup 240}Pu, {sup 241}Am, and {sup 237}Np) in the penetrators indicates that at least part of the uranium originated from the reprocessing of nuclear fuel. Because the concentrations of

IAEA sends out samples of uranium ore

Energy Technology Data Exchange (ETDEWEB)

NONE

1966-06-15

Full text: Governments and organizations interested in developing uranium resources will be assisted by a new service, now being inaugurated by the Agency's laboratories, for the distribution of reference samples of uranium ores. This is an addition to the service which began at Seibersdorf in January 1962 for the distribution of calibrated radionuclides, and which has met with a steadily increasing demand. * Uranium deposits consisting of ores with a uranium content in the range 0.5 - 0.05 per cent occur in a number of countries, including developing countries and can present considerable analytical difficulties. In 1962 the Agency asked Member States whether they would be interested in receiving reference samples of uranium ores to assist them in checking their methods of chemical analysis. The response encouraged the Agency to proceed. There is a multiplicity of types of uranium ores and, initially, three of the most commonly occurring have been selected - torbernite, uraninite and carnotite. Member States have provided the laboratory with supplies of these three types of ore. In order to determine the uranium content, samples are sent to leading laboratories throughout the world, so as to arrive at the most accurate values possible. This work has proved to be useful to the laboratories themselves ; in searching for reasons for discrepancies between the different collaborating laboratories, they enlarge their own knowledge and improve their methods. The reference samples are sent out in the form of fine powder, and are available to atomic energy commissions, research laboratories or mining companies. The requesting laboratory, having worked out the analytical process best suited to its needs, is then able to check its results by analysing an IAEA reference sample of known uranium content. By the end of 1966, reference samples will be available of the three ores mentioned, and later also of pure uranium oxide and of uranium oxide containing trace impurities, the

Uranium isotopes in ground water as a prospecting technique

International Nuclear Information System (INIS)

Cowart, J.B.; Osmond, J.K.

1980-02-01

The isotopic concentrations of dissolved uranium were determined for 300 ground water samples near eight known uranium accumulations to see if new approaches to prospecting could be developed. It is concluded that a plot of 234 U/ 238 U activity ratio (A.R.) versus uranium concentration (C) can be used to identify redox fronts, to locate uranium accumulations, and to determine whether such accumulations are being augmented or depleted by contemporary aquifer/ground water conditions. In aquifers exhibiting flow-through hydrologic systems, up-dip ground water samples are characterized by high uranium concentration values (> 1 to 4 ppB) and down-dip samples by low uranium concentration values (less than 1 ppB). The boundary between these two regimes can usually be identified as a redox front on the basis of regional water chemistry and known uranium accumulations. Close proximity to uranium accumulations is usually indicated either by very high uranium concentrations in the ground water or by a combination of high concentration and high activity ratio values. Ground waters down-dip from such accumulations often exhibit low uranium concentration values but retain their high A.R. values. This serves as a regional indicator of possible uranium accumulations where conditions favor the continued augmentation of the deposit by precipitation from ground water. Where the accumulation is being dispersed and depleted by the ground water system, low A.R. values are observed. Results from the Gulf Coast District of Texas and the Wyoming districts are presented

The use of depleted uranium in II Gulf War and its impact on Iraq and the perspective of international law

International Nuclear Information System (INIS)

Yahya, Ali Mahmood

2012-01-01

In the piece radioactive depleted uranium is a mineral density of 1.7 times heavier than lead a radiation active low level remains on the uranium used as fuel in nuclear reactors or after the manufacture of atomic bombs, and when it enters this dust into the body either by breathing or eating it causes harm caused by toxic chemotherapy and radiation in each of the bronchi and bronchial lung damage and also damage to the kidneys, liver, bone and the incidence of cancer and the potential for causing damage to the gene, Americans and British used between 300-800 tons of depleted uranium irradiated in ammunition were distributed in the deserts of Kuwait and southern Iraq in the 1991 II Gulf War when it began U.S. tanks, planes and Warthog A-10 using this ammunition against the Iraqi army Russian was measured by the level of radiation in the region by the Environmental Engineering of the Faculty of Engineering at the University of Baghdad and found equal to that between several hundred to a thousand times the natural level of radiation to the soil of lraq, which is (70 bq/kg) of the soil and congenital malformations of newborns has increased 7 times the rate in 1990 as the use of depleted uranium in the war against Iraq caused thousands of cancer cases among civilians in the Iraq and the so-called symptoms of Gulf War illness or disease, the curse of Iraq suffered by many soldiers, members of the U.S. and Europe are due to exposure to radiation from depleted uranium, in addition to this has started to show thousands of cases of deformity among Iraqi children who were born after the war and the high proportion of children of war veterans were born and their distortions or suffering from acute illness. The Piece Universal Declaration of Human Rights and the African Charter of Human Rights and the Treaty of the Organization of Armed Conflict, Conventions and Protocols to the Four Geneva and UN Resolution 1540, for the year 2004, and the principles of international law are

Study on the effect factor of the absolute fission rates measured by depleted uranium fission chamber

International Nuclear Information System (INIS)

Jiang Li; Liu Rong; Wang Dalun; Wang Mei; Lin Jufang; Wen Zhongwei

2003-01-01

The absolute fission rates was measured by the depleted uranium fission chamber. The efficiency of the fission fragments recorded in the fission chamber was analyzed. The factor influencing absolute fission rates was studied in the experiment, including the disturbing effect between detectors and the effect of the structural of the fission chamber, etc

Determination of uranium in samples containing bulk aluminium

International Nuclear Information System (INIS)

Das, S.K.; Kannan, R.; Dhami, P.S.; Tripathi, S.C.; Gandhi, P.M.

2015-01-01

The determination of uranium is of great importance in PUREX process and need to be analyzed at different concentration ranges depending on the stage of reprocessing. Various techniques like volumetry, spectrophotometry, ICP-OES, fluorimetry, mass spectrometry etc. are used for the measurement of uranium in these samples. Fast and sensitive methods suitable for low level detection of uranium are desirable to cater the process needs. Microgram quantities of uranium are analyzed by spectrophotometric method using 2-(5- bromo-2-pyridylazo-5-diethylaminophenol) (Br-PADAP) as the complexing agent. But, the presence of some of the metal ions viz. Al, Pu, Zr etc. interferes in its analysis. Therefore, separation of uranium from such interfering metal ions is required prior to its analysis. This paper describes the analysis of uranium in samples containing aluminium as major matrix

Evaluation of depleted uranium in the environment at Aberdeen Proving Grounds, Maryland and Yuma Proving Grounds, Arizona. Final report

International Nuclear Information System (INIS)

Kennedy, P.L.; Clements, W.H.; Myers, O.B.; Bestgen, H.T.; Jenkins, D.G.

1995-01-01

This report represents an evaluation of depleted uranium (DU) introduced into the environment at the Aberdeen Proving Grounds (APG), Maryland and Yuma Proving Grounds (YPG) Arizona. This was a cooperative project between the Environmental Sciences and Statistical Analyses Groups at LANL and with the Department of Fishery and Wildlife Biology at Colorado State University. The project represents a unique approach to assessing the environmental impact of DU in two dissimilar ecosystems. Ecological exposure models were created for each ecosystem and sensitivity/uncertainty analyses were conducted to identify exposure pathways which were most influential in the fate and transport of DU in the environment. Research included field sampling, field exposure experiment, and laboratory experiments. The first section addresses DU at the APG site. Chapter topics include bioenergetics-based food web model; field exposure experiments; bioconcentration by phytoplankton and the toxicity of U to zooplankton; physical processes governing the desorption of uranium from sediment to water; transfer of uranium from sediment to benthic invertebrates; spead of adsorpion by benthic invertebrates; uptake of uranium by fish. The final section of the report addresses DU at the YPG site. Chapters include the following information: Du transport processes and pathway model; field studies of performance of exposure model; uptake and elimination rates for kangaroo rates; chemical toxicity in kangaroo rat kidneys

Evaluation of depleted uranium in the environment at Aberdeen Proving Grounds, Maryland and Yuma Proving Grounds, Arizona. Final report

Energy Technology Data Exchange (ETDEWEB)

Kennedy, P.L.; Clements, W.H.; Myers, O.B.; Bestgen, H.T.; Jenkins, D.G. [Colorado State Univ., Fort Collins, CO (United States). Dept. of Fishery and Wildlife Biology

1995-01-01

This report represents an evaluation of depleted uranium (DU) introduced into the environment at the Aberdeen Proving Grounds (APG), Maryland and Yuma Proving Grounds (YPG) Arizona. This was a cooperative project between the Environmental Sciences and Statistical Analyses Groups at LANL and with the Department of Fishery and Wildlife Biology at Colorado State University. The project represents a unique approach to assessing the environmental impact of DU in two dissimilar ecosystems. Ecological exposure models were created for each ecosystem and sensitivity/uncertainty analyses were conducted to identify exposure pathways which were most influential in the fate and transport of DU in the environment. Research included field sampling, field exposure experiment, and laboratory experiments. The first section addresses DU at the APG site. Chapter topics include bioenergetics-based food web model; field exposure experiments; bioconcentration by phytoplankton and the toxicity of U to zooplankton; physical processes governing the desorption of uranium from sediment to water; transfer of uranium from sediment to benthic invertebrates; spead of adsorpion by benthic invertebrates; uptake of uranium by fish. The final section of the report addresses DU at the YPG site. Chapters include the following information: Du transport processes and pathway model; field studies of performance of exposure model; uptake and elimination rates for kangaroo rates; chemical toxicity in kangaroo rat kidneys.

Packaging and Disposal of a Radium-beryllium Source using Depleted Uranium Polyethylene Composite Shielding

International Nuclear Information System (INIS)

Keith Rule; Paul Kalb; Pete Kwaschyn

2003-01-01

Two, 111-GBq (3 Curie) radium-beryllium (RaBe) sources were in underground storage at the Brookhaven National Laboratory (BNL) since 1988. These sources originated from the Princeton Plasma Physics Laboratory (PPPL) where they were used to calibrate neutron detection diagnostics. In 1999, PPPL and BNL began a collaborative effort to expand the use of an innovative pilot-scale technology and bring it to full-scale deployment to shield these sources for eventual transport and burial at the Hanford Burial site. The transport/disposal container was constructed of depleted uranium oxide encapsulated in polyethylene to provide suitable shielding for both gamma and neutron radiation. This new material can be produced from recycled waste products (depleted uranium and polyethylene), is inexpensive, and can be disposed with the waste, unlike conventional lead containers, thus reducing exposure time for workers. This paper will provide calculations and information that led to the initial design of the shielding. We will also describe the production-scale processing of the container, cost, schedule, logistics, and many unforeseen challenges that eventually resulted in the successful fabrication and deployment of this shield. We will conclude with a description of the final configuration of the shielding container and shipping package along with recommendations for future shielding designs

Depleted uranium as a by product of nuclear technology

International Nuclear Information System (INIS)

Orlic, M.

2000-01-01

Depleted uranium (DU) has been used during the War in Yugoslavia in the year 1999 by NATO forces, as well as in Bosnia and Gulf War. In Yugoslavia it has been used in two modalities: as ammunition (mostly caliber 30 mm) and as a part of cruise missiles (counterweight penetrator). Total amount of DU in Yugoslavia was about 10 tons. DU is a by product of nuclear technology and represents low-level nuclear waste. Therefore it should be stored. But, because of military application it is in the environment where it could react chemo toxically or radio toxically and so endanger people and animals. This paper contains all relevant technology parameters of DU created as a by product, DU physical and chemical properties, DU ammunition effects, environmental DU transport, and estimation of consequences on people and environment

Nuclear forensic analysis of uranium oxide powders interdicted in Victoria, Australia

Energy Technology Data Exchange (ETDEWEB)

Kristo, Michael Joseph [Lawrence Livermore National Laboratory, Livermore, CA (United States); Keegan, Elizabeth; Colella, Michael [Australian Nuclear Science and Technology Organisation, Kirrawee, NSW (Australia); and others

2015-07-01

Nuclear forensic analysis was conducted on two uranium samples confiscated during a police investigation in Victoria, Australia. The first sample, designated NSR-F-270409-1, was a depleted uranium powder of moderate purity (∝ 1000 μg/g total elemental impurities). The chemical form of the uranium was a compound similar to K{sub 2}(UO{sub 2}){sub 3}O{sub 4} . 4H{sub 2}O. While aliquoting NSR-F-270409-1 for analysis, the body and head of a Tineid moth was discovered in the sample. The second sample, designated NSR-F-270409-2, was also a depleted uranium powder. It was of reasonably high purity (∝ 380 μg/g total elemental impurities). The chemical form of the uranium was primarily UO{sub 3} . 2H{sub 2}O, with minor phases of U{sub 3}O{sub 8} and UO{sub 2}. While aliquoting NSR-F-270409-2 for analysis, a metal staple of unknown origin was discovered in the sample. The presence of {sup 236}U and {sup 232}U in both samples indicates that the uranium feed stocks for these samples experienced a neutron flux at some point in their history. The reactor burn-up calculated from the isotopic composition of the uranium is consistent with that of spent fuel from natural uranium (NU) fueled Pu production. These nuclear forensic conclusions allow us to categorically exclude Australia as the origin of the material and greatly reduce the number of candidate sources.

Contamination by depleted uranium (Du) in South Serbia

International Nuclear Information System (INIS)

Popovic, L.; Todorovic, J.; Bozic, P.; Stevanovic, Z.

2006-01-01

The paper present the results of the study on D.U. (depleted uranium) contamination in the environment and possible effects on animal healths in the region o f Bujanovac. Samples of soil, feed, leaves, grass, lichen, moss, honey and water were collected randomly in 2003/2004 in the vicinity of the target area (500-1000 m) and 5 km from the target area. Activity of the radionuclides ( 226 Ra, 232 Th, 40 K, 210 Pb, 238 U, 235 U, 137 Cs, 7 Be) in soils, grass, lichen, moss and honey was determined on Hp Ge detector (Canberra, relative efficiency 23%) by standard gamma spectrometry. Total alpha and beta activity in water was determined on proportional alpha/beta counter (Canberra 2400, efficiency for alpha emitters 11%, efficiency for beta emitters 30%). Non significantly higher values of concentrations of 226 Ra, 232 Th, 238 U and 235 U were measured in the immediate vicinity of the targeted site, but 235 U/ 238 U activity ratio in soils indicated the natural origin of uranium. On both sites the contents of radionuclides in soils were in the range of values measured in soils in Belgrade (2002-2005), at the mountain Stara Planina (1999) and in the region. The soil was found to be poor in potassium. In mosses and lichen, high concentrations of 137 Cs, 7 Be, 226 Ra and 210 Pb were found, while in leaves and grass there were lower concentrations of K, due to soil poor in K. As for uranium, there were no significant variations due to the sites, and 235 U/ 238 U activity ratios were close to values measured in vegetation in the vicinity of power plants 0.07-0.08. In honey, both 238 U and 235 U were below the minimal detectable concentrations. Total alpha and total beta activities measured in water showed no significant differences between the sites, and the obtained values were in range of the permissible values for drinking water in S.M.N. (total alpha activity <0.1 Bq/L, total beta activity <1 Bq/L) Samples of blood of cows and sheep bred in the area were collected

Renal dysfunction induced by long-term exposure to depleted uranium in rats

Energy Technology Data Exchange (ETDEWEB)

Zhu, Guoying; Xiang, Xiqiao; Chen, Xiao; Wang, Lihua; Hu, Heping; Weng, Shifang [Fudan University, Institute of Radiation Medicine, Shanghai (China)

2009-01-15

Depleted uranium (DU) is a kind of radioactive heavy metal which can enter into the body via inhalation (aerosols), ingestion (drinking and eating) and wounds (embedded), and causes chemical and/or radiation-induced toxicities. In this study, male Sprague Dawley rats were surgically implanted in gastrocnemius muscle with DU fragments at three dose levels (low-dose, medium-dose and high-dose), with biologically inert tantalum (Ta) fragments served as controls. At 1 day, 7 days, and 3, 6, and 12 months after implantation, the rats were euthanized and tissue samples were collected, and uranium levels were measured in a variety of tissues by inductively coupled plasma-mass spectrometry (ICP-MS) to analyze the dynamic changes and distribution of uranium in rats. Thereafter, at 3, 6 and 12 months after implantation, the rats were euthanized after the collection of 24 h urine, blood and kidney samples were collected for analysis of DU-induced renal histopathologic changes and renal dysfunction. It was observed that DU concentrations in all the DU implanted groups were higher than that in Ta control group, and DU concentrations in the kidney increased with the implanted times, peaked at the 90 days after implantation, with a high correlation to the implanted DU doses, and then began to decrease gradually and slowly, and the DU concentrations in kidney still maintained at a relatively high level even at the 360 days after implantation. Otherwise, chronic DU contamination could induce the pathological changes of renal glomeruli, tubules and mesenchyme, such as interstitial fibrosis, enlarged interstice of renal tubular epithelial cells, tumefactions and necrosis of epithelial cells, shrinkage and disappearance of cavity of Bowman's capsule. By TEM, it was shown that the basement membrane of glomerulus was incrassated, mitochondrial of kidney proximal tubule had visible tumefaction and became bigger, and the mitochondrial cristae became shorter and disorderly in

Renal dysfunction induced by long-term exposure to depleted uranium in rats

International Nuclear Information System (INIS)

Zhu, Guoying; Xiang, Xiqiao; Chen, Xiao; Wang, Lihua; Hu, Heping; Weng, Shifang

2009-01-01

Depleted uranium (DU) is a kind of radioactive heavy metal which can enter into the body via inhalation (aerosols), ingestion (drinking and eating) and wounds (embedded), and causes chemical and/or radiation-induced toxicities. In this study, male Sprague Dawley rats were surgically implanted in gastrocnemius muscle with DU fragments at three dose levels (low-dose, medium-dose and high-dose), with biologically inert tantalum (Ta) fragments served as controls. At 1 day, 7 days, and 3, 6, and 12 months after implantation, the rats were euthanized and tissue samples were collected, and uranium levels were measured in a variety of tissues by inductively coupled plasma-mass spectrometry (ICP-MS) to analyze the dynamic changes and distribution of uranium in rats. Thereafter, at 3, 6 and 12 months after implantation, the rats were euthanized after the collection of 24 h urine, blood and kidney samples were collected for analysis of DU-induced renal histopathologic changes and renal dysfunction. It was observed that DU concentrations in all the DU implanted groups were higher than that in Ta control group, and DU concentrations in the kidney increased with the implanted times, peaked at the 90 days after implantation, with a high correlation to the implanted DU doses, and then began to decrease gradually and slowly, and the DU concentrations in kidney still maintained at a relatively high level even at the 360 days after implantation. Otherwise, chronic DU contamination could induce the pathological changes of renal glomeruli, tubules and mesenchyme, such as interstitial fibrosis, enlarged interstice of renal tubular epithelial cells, tumefactions and necrosis of epithelial cells, shrinkage and disappearance of cavity of Bowman's capsule. By TEM, it was shown that the basement membrane of glomerulus was incrassated, mitochondrial of kidney proximal tubule had visible tumefaction and became bigger, and the mitochondrial cristae became shorter and disorderly in alignment

Examination of disks from the IPNS depleted uranium target

International Nuclear Information System (INIS)

Strain, R.V.; Carpenter, J.M.

1995-10-01

This report describes the results of examining the Zircaloy-2 clad depleted uranium disks from the Intense Pulse Neutron Source (IPNS) Target. That target operated from August, 1981 to June, 1988 and from September, 1991 to September, 1992 at 450 MeV, pulsing at 30 Hz with a time average proton current of about 15 microA. The target was removed from service when the presence of fission products ( 135 Xe) in the coolant cover gas indicated a failure in the Zircaloy-2 cladding. Altogether, the target had absorbed about 240 mA hours of proton current, and endured between 50,000 and 100,000 thermal cycles. The purpose of the examination was to assess the condition of the disks and determine the cause of the cladding failure. The results of visual, gamma ray scanning, and destructive metallurgical examination of two disks are described

Experimental study on full-scale ZrCo and depleted uranium beds applied for fast recovery and delivery of hydrogen isotopes

International Nuclear Information System (INIS)

Kou, Huaqin; Huang, Zhiyong; Luo, Wenhua; Sang, Ge; Meng, Daqiao; Luo, Deli; Zhang, Guanghui; Chen, Hao; Zhou, Ying; Hu, Changwen

2015-01-01

Highlights: • Thin double-layered annulus beds with ZrCo and depleted uranium were fabricated. • Depleted uranium bed delivered 16.41 mol H 2 at rate of 20 Pa m 3 /s within 30 min. • The delivery property of depleted uranium bed was very stable during the 10 cycles. - Abstract: Metal hydride bed is an important component for the deuterium–tritium fusion energy under development in International Thermonuclear Experimental Reactor (ITER), in which the hydrogen recovery and delivery properties are influenced by the bed configuration, operation conditions and the hydrogen storage materials contained in the bed. In this work, a thin double-layered annulus bed configuration was adopted and full-scale beds loaded with ZrCo and depleted uranium (DU) for fast recovery and delivery of hydrogen isotopes were fabricated. The properties of hydrogen recovery/delivery together with the inner structure variation in the fabricated beds were systematically studied. The effects of operation conditions on the performances of the bed were also investigated. It was found that both of the fabricated ZrCo and DU beds were able to achieve the hydrogen storage target of 17.5 mol with fast recovery rate. In addition, experimental results showed that operation of employing extra buffer vessel and scroll pump could not only promote the hydrogen delivery process but also reduce the possibility about disproportionation of ZrCo. Compared with ZrCo bed, DU bed exhibited superior hydrogen delivery performances in terms of fast delivery rate and high hydrogen delivery amount, which could deliver over 16.4 mol H 2 (93.7% of recovery amount) within 30 min at the average delivery rate of 20 Pa m 3 /s. Good reversibility as high as 10 cycles without obvious degradation tendency in both of hydrogen delivery amount and delivery rate for DU bed was also achieved in our study. It was suggested that the fabricated thin double-layered annulus DU bed was a good candidate to rapidly deliver and recover

Depleted uranium risk assessment at Aberdeen Proving Ground

International Nuclear Information System (INIS)

Ebinger, M.H.; Myers, O.B.; Kennedy, P.L.; Clements, W.H.

1993-01-01

The Environmental Science Group at Los Alamos and the Test and Evaluation Command (TECOM) are assessing the risk of depleted uranium (DU) testing at Aberdeen Proving Ground (APG). Conceptual and mathematical models of DU transfer through the APG ecosystem have been developed in order to show the mechanisms by which DU migrates or remains unavailable to different flora and fauna and to humans. The models incorporate actual rates of DU transfer between different ecosystem components as much as possible. Availability of data on DU transport through different pathways is scarce and constrains some of the transfer rates that can be used. Estimates of transfer rates were derived from literature sources and used in the mass-transfer models when actual transfer rates were unavailable. Objectives for this risk assessment are (1) to assess if DU transports away from impact areas; (2) to estimate how much, if any, DU migrates into Chesapeake Bay; (3) to determine if there are appreciable risks to the ecosystems due to DU testing; (4) to estimate the risk to human health as a result of DU testing

Uranium

International Nuclear Information System (INIS)

Hamdoun, N.A.

2007-01-01

The article includes a historical preface about uranium, discovery of portability of sequential fission of uranium, uranium existence, basic raw materials, secondary raw materials, uranium's physical and chemical properties, uranium extraction, nuclear fuel cycle, logistics and estimation of the amount of uranium reserves, producing countries of concentrated uranium oxides and percentage of the world's total production, civilian and military uses of uranium. The use of depleted uranium in the Gulf War, the Balkans and Iraq has caused political and environmental effects which are complex, raising problems and questions about the effects that nuclear compounds left on human health and environment.

Quantitative analysis of hydrogen gas formed by aqueous corrosion of metallic uranium

International Nuclear Information System (INIS)

Fonnesbeck, J.

2000-01-01

Three unirradiated EBR-II blanket fuel samples containing depleted uranium metal were corrosion tested in simulated J-13 well water at 90 C. The corrosion rate of the blanket uranium metal was then determined relative to H 2 formation. Corrosion of one of the samples was interrupted prior to complete oxidation of the uranium metal and the solid corrosion product was analyzed for UO 2 and UH 3

Quantitative analysis of hydrogen gas formed by aqueous corrosion of metallic uranium

Energy Technology Data Exchange (ETDEWEB)

Fonnesbeck, J.

2000-03-20

Three unirradiated EBR-II blanket fuel samples containing depleted uranium metal were corrosion tested in simulated J-13 well water at 90 C. The corrosion rate of the blanket uranium metal was then determined relative to H{sub 2} formation. Corrosion of one of the samples was interrupted prior to complete oxidation of the uranium metal and the solid corrosion product was analyzed for UO{sub 2} and UH{sub 3}.

Remediation of soils contaminated with particulate depleted uranium by multi stage chemical extraction.

Science.gov (United States)

Crean, Daniel E; Livens, Francis R; Sajih, Mustafa; Stennett, Martin C; Grolimund, Daniel; Borca, Camelia N; Hyatt, Neil C

2013-12-15

Contamination of soils with depleted uranium (DU) from munitions firing occurs in conflict zones and at test firing sites. This study reports the development of a chemical extraction methodology for remediation of soils contaminated with particulate DU. Uranium phases in soils from two sites at a UK firing range, MOD Eskmeals, were characterised by electron microscopy and sequential extraction. Uranium rich particles with characteristic spherical morphologies were observed in soils, consistent with other instances of DU munitions contamination. Batch extraction efficiencies for aqueous ammonium bicarbonate (42-50% total DU extracted), citric acid (30-42% total DU) and sulphuric acid (13-19% total DU) were evaluated. Characterisation of residues from bicarbonate-treated soils by synchrotron microfocus X-ray diffraction and X-ray absorption spectroscopy revealed partially leached U(IV)-oxide particles and some secondary uranyl-carbonate phases. Based on these data, a multi-stage extraction scheme was developed utilising leaching in ammonium bicarbonate followed by citric acid to dissolve secondary carbonate species. Site specific U extraction was improved to 68-87% total U by the application of this methodology, potentially providing a route to efficient DU decontamination using low cost, environmentally compatible reagents. Copyright © 2013 The Authors. Published by Elsevier B.V. All rights reserved.

Final programmatic environmental impact statement for alternative strategies for the long-term management and use of depleted uranium hexafluoride. Volume 3: Responses to public comments

International Nuclear Information System (INIS)

1999-04-01

This PEIS assesses the potential impacts of alternative management strategies for depleted uranium hexafluoride (UF 6 ) currently stored at three DOE sites: Paducah site near Paducah, Kentucky, Portsmouth site near Portsmouth, Ohio; and K-25 site on the Oak Ridge Reservation, Oak Ridge, Tennessee. The alternatives analyzed in the PEIS include no action, long-term storage as UF 6 , long-term storage as uranium oxide, use as uranium oxide, use as uranium metal, and disposal. DOE's preferred alternative is to begin conversion of the depleted UF 6 inventory as soon as possible, either to uranium oxide, uranium metal, or a combination of both, while allowing for use of as much of this inventory as possible. This volume of the Final PEIS contains the comments and DOE's responses to comments received during the comment period. Chapter 2 contains photocopies of written submissions received by DOE on the Draft PEIS; DOE's responses to those comments are listed in Chapter 3. Chapter 4 provides the oral comments received at the public hearings and DOE's responses. Chapter 5 provides indices to comments and responses arranged by commentor name and by comment number

Destroying of chemical and oil industry, bombing of energy sources and use of depleted uranium ammunition during NATO bombing in FR Yugoslavia

International Nuclear Information System (INIS)

Antic, D. P.

2002-01-01

During the NATO bombing of the FR Yugoslavia from March 24 to June 10, 1999, according to NATO's data, there were 34 250 takeoffs of the 1200 aircrafts; 367 000 tonnes of kerosine were consumed; there were 400 Tomahawk cruise missiles and 130 air-to-ground missiles. It is estimated that 22 000-79 000 tonnes of explosives were dropped; in addition to 20 000 smart bombs and 5000 conventional bombs of various weight and purposes. The bombing had the characteristics of an ecological war, among other things. During the air strikes A-10 aircrafts fired shells with depleted uranium from 30 mm guns. According to NATO estimates, around 31 000 projectiles were fired (298 g of depleted uranium for each bullet, and more than 10 tonnes of uranium-238 as a contaminating agent), and according to the Yugoslav Army estimated, around 50 000 were fired. Some radiological, chemical and ethical consequences of NATO bombing in FR Yugoslavia are reviewed. (author)

Determination of uranium in industrial and environmental samples. Vol. 4

Energy Technology Data Exchange (ETDEWEB)

El-Sweify, F H; Shehata, M K; Metwally, E M; El-Shazly, E A.A.; El-Naggar, H A [Nuclear Chemistry Department, Hot Laborities Center, Atomic Energy Authority, Cairo (Egypt)

1996-03-01

The phosphate ores used at `Abu zaabal fertilizer and chemical company` for the production of some chemicals and fertilizers contain detectable amounts of uranium. In this study, the content of uranium in samples of different products of fertilizers, gypsum, and phosphate ore were determined using NAA, and gamma ray spectroscopy of the irradiated samples. Another method based on measuring the natural radioactivity of {sup 238} U series for non-irradiated samples using gamma-ray spectroscopy was also used for determine uranium content in the samples. In the NAA method, the content of U(ppm) in the samples was been computed from the photopeak activity of the lines = 106.1, 228.2, and 277.5 KeV of {sup 239} Np induced in the irradiated samples, and the uranium standard simultaneously irradiated. the gamma-ray spectra, and the decay curves are given. In the second method the gamma-ray spectra of the natural radioactivity of the samples and uranium standard were measured. The gamma-transition of energies 295.1, 251.9 KeV for {sup 214} Pb; 609.3, 768.4, 1120.3, 1238.1 KeV for {sup 214} Bi were determined. The uranium {sup 23U} traces in drainage water was also determined spectrophotometrically using arsenazo-III after preconcentration of uranium from the pretreated drainage water in column packed with chelex-100 resin. The recovery was found to be 90 {+-} 5%. 11 figs., 3 tabs.

Effects of chelating agent CBMIDA on the toxicity of depleted uranium administered subcutaneously in rats

International Nuclear Information System (INIS)

Fukuda, Satoshi; Ikeda, Mizuyo; Nakamaura, Mariko

2008-01-01

We examined the acute toxicity of depleted uranium (DU) after subcutaneous injection as a simulated wounds model, and the effects of the chelating agent catechol-3,6-bis(methyliminodiacetic acid) (CBMIDA), by local treatment in rats. First, to examine the initial behavior and toxicity of uranium of different chemical forms, male Wistar rats were subcutaneously injected with 4 and 16 mg/kg DU (pH 1) in a solution of pH 1 and 7, respectively, and were killed 1, 3, 6 and 24 hours later. After the injection of DU(pH1), about 60% of the uranium was retained for first 1-3 hours at the injected sites, and then decreased to 16% at 24 hours in the 4 mg/kg DU group; however, the uranium did not change significantly in the 16 mg/kg DU group. Urinary excretion rates of uranium increased in a time-independent manner after the injection Depositions of uranium in the liver, kidneys and femur were found at 1 hour after DU injection, with significant increases in serum and urinary biochemical markers indicating acute and severe damage. The results of the DU (pH 7) injection were useful for estimating the toxicity of uranium by the chemical changes in the body. Second, CBMIDA (480 mg/kg) was infused into the DU-injected site at 0, 10, 30, 60 min and 24 hours after the subcutaneous injection of 4 mg/kg DU (pH 1 and 7). When CBMIDA was administered within 120 min after DU (pH 1) injection, the uranium at the injected sites decreased to 4-17% of that in the no-treatment DU (pH 1) group, and was excreted effectively in the urine and feces, with decreased levels in the kidneys and femur. The results indicated that the subcutaneously injected uranium acutely induced severe damage in the DU-injected sites and organs after DU intake, relating to chemical forms of uranium by pH and that local treatment of CBMIDA was effective in decreasing the acute toxicity of uranium if carried out as early as possible (at least within 2 hours) after DU administration. (author)

Remediation application strategies for depleted uranium contaminated soils at the US Army Yuma Proving Ground

International Nuclear Information System (INIS)

Vandel, D.S.; Medina, S.M.; Weidner, J.R.

1994-03-01

The US Army Yuma Proving Ground (YPG), located in the southwest portion of Arizona conducts firing of projectiles into the Gunpoint (GP-20) firing range. The penetrators are composed of titanium and DU. The purpose of this project was to determine feasible cleanup technologies and disposal alternatives for the cleanup of the depleted uranium (DU) contaminated soils at YPG. The project was split up into several tasks that include (a) collecting and analyzing samples representative of the GP-20 soils, (b) evaluating the data results, (c) conducting a literature search of existing proven technologies for soil remediation, and (0) making final recommendations for implementation of this technology to the site. As a result of this study, several alternatives for the separation, treatment, and disposal procedures are identified that would result in meeting the cleanup levels defined by the Nuclear Regulatory Commission for unrestricted use of soils and would result in a significant cost savings over the life of the firing range

Epi-genetics modifications induced by a depleted uranium exposure in the zebra fish

Energy Technology Data Exchange (ETDEWEB)

Gombeau, K.; Pereira, S.; Adam-Guillermin, C. [IRSN/PRP-ENV/SERIS/LECO (France); Bourdineaud, J.P. [UMR CNRS 5805 EPOC (France); Ravanat, J.L. [INAC/Scib UMR E3 CEA-UJF (France)

2014-07-01

The work presented here integrates in the general framework of assessment of effects of chronic exposure to low doses of radionuclides. This evaluation necessarily involves the study of the mechanisms of toxic action at the cellular or subcellular level, in order to better understand the processes of propagation of effects to the level of the populations or ecosystems. As such, the question of the mechanisms underlying the trans-generational effects and the adaptive capacity of organisms is central, both in humans and in animal species. Epigenetic refer to changes in gene function that do not involve changes in DNA sequence, and which are transmitted in a hereditary manner by mitosis or meiosis. The latter plays a key role in these trans-generational effects. Among these changes, DNA-methylation is one of the most studied epigenetic parameters. This work is part of a PhD, included in the European COMET project (Euratom 7. Framework Program), and focuses on epigenetic modifications induced in zebra fish after a chronic exposure to radionuclides. Male and female fishes were exposed to 2 and 20 μg.L{sup -1} of depleted uranium for 24 days. After 7 and 24 days of exposure, brain, gonads, and eyes were collected in order to study changes in DNA methylation. In addition, genotoxicity was measured by the γH2AX assay. The overall changes in DNA methylation were studied by AFLP-MS and HPLC-MS, in order to know if the exposure to depleted uranium changes the global status of DNA methylation. We have found a decrease in the global level of methylation in the eyes of males after 24 days of exposure, the diminution being much more important and significant at the higher concentration of exposure (11.79 ± 3.62 against 52.43 ± 3.01 for controls) This study will be refined by analyzing the methylation of specific regions of the genome, because it represent the sequences of genes involved in major physiological functions and that may be subject to variations in the methylation

Re-enrichment of depleted uranium by passage through a gaseous diffusion installation; Reenrichissement de l'uranium appauvri par passage dans une installation de diffusion gazeuse

Energy Technology Data Exchange (ETDEWEB)

Lagrange, P; Billous, O [Commissariat a l' Energie Atomique, Saclay (France). Centre d' Etudes Nucleaires

1958-07-01

The reader will find in this paper an economic study of the re-utilization of depleted uranium from nuclear reactors, whether its content be above or under natural proportions. Re-utilization is possible either through bringing the depleted product up to its initial content of {sup 235}U by mixture with a richer concentrate, or else by passing it through a gaseous diffusion plant. The economic area of such re-utilization depends on a number of considerations. We give a general study of it, with reference to some typical gaseous diffusion facilities. (author)Fren. [French] Ce rapport examine au point de vue economique la reutilisation de l'uranium appauvri provenant des reacteurs nucleaires, qu'il soit indifferemment en dessus ou en dessous de la teneur naturelle. Cette reutilisation peut se faire soit en ramenant le produit a sa teneur initiale en isotope 235 par un melange convenable avec un concentre plus riche, soit en le faisant passer dans une usine de Diffusion Gazeuse. La zone de rentabilite de cette reutilisation depend de diverses conditions economiques. Elle est etudiee ci-dessous d'une maniere generale, puis en se referant a des installations-type de diffusion gazeuse. (auteur)

Determination of uranium in clinical and environmental samples by FIAS-ICPMS

International Nuclear Information System (INIS)

Karpas, Z.; Lorber, A.; Halicz, L.; Gavrieli, I.

1998-01-01

Uranium may enter the human body through ingestion or inhalation. Ingestion of uranium compounds through the diet, mainly drinking water, is a common occurrence, as these compounds are present in the biosphere. Inhalation of uranium-containing particles is mainly an occupational safety problem, but may also take place in areas where uranium compounds are abundant. The uranium concentration in urine samples may serve as an indication of the total uranium body content. A method based on flow injection and inductively coupled plasma mass spectrometry (FIAS-ICPMS) was found to be most suitable for determination of uranium in clinical samples (urine and serum), environmental samples (seawater, wells and carbonate rocks) and in liquids consumed by humans (drinking water and commercial beverages). Some examples of the application of the FIAS-ICPMS method are reviewed and presented here

Determination of uranium in liquid samples

International Nuclear Information System (INIS)

Macefat, Martina R.; Grahek, Zeljko; Ivsic, Astrid G.

2008-01-01

Full text: Uranium is a natural occurring radionuclide and the first member of natural radioactive chains which makes its determination in natural materials interesting from geochemical and radioecological aspect. It can be quantitatively determined as element and/or its radioisotopes by different spectrometric methods (ICP-MS, spectrophotometry, alpha spectrometry). It is necessary to develop inexpensive, rapid and sensitive methods for the routine analysis. Therefore, in this paper, development of a new method for the isolation of uranium from liquid samples and subsequent determination by spectrophotometry and ICP-MS will be described. It is possible to isolate uranium from drinking and seawater using extraction chromatography or mixed solvent ion exchange. Uranium can be strongly bound on the TRU extraction chromatographic resin from nitric acid (chemical recovery is 100%) and can be separated from other interfering elements, while separation from thorium, which can be also strongly bound on this resin, is possible with hydrochloric acid. It is also possible to separate uranium from thorium on the anion exchanger Amberlite CG-400 (NO 3 - form) because uranium is much more weakly bound on this exchanger from alcoholic solutions of nitric acid. After the separation uranium is determined by ICP-MS and by spectrophotometric method with arsenazo III (λ max =652 nm). Developed method enables selection of the optimal mode of isolation for the given purposes. (author)

Uranium content measurement in drinking water samples using track etch technique

International Nuclear Information System (INIS)

Kumar, Mukesh; Kumar, Ajay; Singh, Surinder; Mahajan, R.K.; Walia, T.P.S.

2003-01-01

The concentration of uranium has been assessed in drinking water samples collected from different locations in Bathinda district, Punjab, India. The water samples are taken from hand pumps and tube wells. Uranium is determined using fission track technique. Uranium concentration in the water samples varies from 1.65±0.06 to 74.98±0.38 μg/l. These values are compared with safe limit values recommended for drinking water. Most of the water samples are found to have uranium concentration above the safe limit. Analysis of some heavy metals (Zn, Cd, Pb and Cu) in water is also done in order to see if some correlation exists between the concentration of uranium and these heavy metals. A weak positive correlation has been observed between the concentration of uranium and heavy metals of Pb, Cd and Cu

Potentiometric determination of hexavalent uranium in uranium silicide samples

International Nuclear Information System (INIS)

Arlegui, Oscar

1999-01-01

The Chilean Nuclear Energy Commission's Department of Nuclear Materials has among its projects the production of fuels elements for nuclear reactors, and, therefore, the Chemical Analysis Laboratory must have a rapid and reliable method for uranium analysis, to control the uranium concentration during each stage of the production process. For this reason the Chilean Nuclear Energy Commission's Chemical Analysis Laboratory has validated a potentiometric method, which is a modification of the Davies and Gray method proposed by A.R. Eberle. This method uses the Potentiometric Titration Technique and is based on the direct and rapid reduction of uranium (VI) to Uranium (IV), in a concentrated phosphoric acid medium, with excess iron (II) used as a reducing agent. In this medium the excess iron (II) selectively oxidizes to iron (III) with nitric acid, using molybdenum (IV) as a catalyzer, the nitrous acid that is produced is eliminated by adding amidosulfuric acid. The solution is diluted with 1M sulfuric acid and the uranium (IV) obtained is titrated potentiometrically with potassium dichromate in the presence of vanadilic sulfate to obtain a better defined final titration point. The samples were softened with hydrochloric acid and nitric acid and later 50 ml were estimated in a 20% sulfuric acid medium. The analytical method was validated by comparing it with Certified Reference Material (C.R.M.) from the New Brunswick Laboratory (NBL), Metallic Uranium, CRM 112-A. The F Test and the T Test show that the value calculated is less than the tabulated value so the result is traceable to the reference material. The quantification limit, sensitivity, precision and accuracy were quantified for the method

Isotopic measurement of uranium using NP-type chelate resin beads

International Nuclear Information System (INIS)

Wu Lanbi; Chen Wenpo; Wang Shijun

1994-08-01

NP-type chelate resin beads is used as a carrier of samples in the isotopic measurements of uranium by mass spectrometry. The results show that its absorption efficiency for uranium can be greater than 50%. It is one order magnitude higher than that strong basic anion resin, however, the ionization efficiencies of both are almost the same. Therefore, the amount of uranium required for isotopic analysis can be reduced one order of magnitude. This method has been used for isotopic analysis of uranium in NP-type chelate resin beads contained 10 -9 ∼ 10 -7 g uranium. For standard sample UTB-500, the external precision of measurements are within +-0.2%, for natural uranium samples are within +- 0.5%. The application of NP-type chelate resin beads in the isotopic measurement of uranium is a new creative achievement. It has been used in the depletion test of uranium-atomic vapor laser isotope separation

ZPR-3 Assembly 6F : A spherical assembly of highly enriched uranium, depleted uranium, aluminum and steel with an average {sup 235}U enrichment of 47 atom %.

Energy Technology Data Exchange (ETDEWEB)

Lell, R. M.; McKnight, R. D; Schaefer, R. W.; Nuclear Engineering Division

2010-09-30

Over a period of 30 years, more than a hundred Zero Power Reactor (ZPR) critical assemblies were constructed at Argonne National Laboratory. The ZPR facilities, ZPR-3, ZPR-6, ZPR-9 and ZPPR, were all fast critical assembly facilities. The ZPR critical assemblies were constructed to support fast reactor development, but data from some of these assemblies are also well suited for nuclear data validation and to form the basis for criticality safety benchmarks. A number of the Argonne ZPR/ZPPR critical assemblies have been evaluated as ICSBEP and IRPhEP benchmarks. Of the three classes of ZPR assemblies, engineering mockups, engineering benchmarks and physics benchmarks, the last group tends to be most useful for criticality safety. Because physics benchmarks were designed to test fast reactor physics data and methods, they were as simple as possible in geometry and composition. The principal fissile species was {sup 235}U or {sup 239}Pu. Fuel enrichments ranged from 9% to 95%. Often there were only one or two main core diluent materials, such as aluminum, graphite, iron, sodium or stainless steel. The cores were reflected (and insulated from room return effects) by one or two layers of materials such as depleted uranium, lead or stainless steel. Despite their more complex nature, a small number of assemblies from the other two classes would make useful criticality safety benchmarks because they have features related to criticality safety issues, such as reflection by soil-like material. ZPR-3 Assembly 6 consisted of six phases, A through F. In each phase a critical configuration was constructed to simulate a very simple shape such as a slab, cylinder or sphere that could be analyzed with the limited analytical tools available in the 1950s. In each case the configuration consisted of a core region of metal plates surrounded by a thick depleted uranium metal reflector. The average compositions of the core configurations were essentially identical in phases A - F. ZPR-3

Health and environmental effects of depleted uranium

International Nuclear Information System (INIS)

Millar, W.A.

2001-01-01

Knowledge accumulated till the end of the 20th century is mentioned briefly. More attention is paid to recent findings. Recent studies of uranium contamination of the Persian Gulf and Balkan War veterans have been conducted in the U.S. and Canada by studying distribution of isotopes of DU in the veterans of the NATO and Allied forces who were accidentally contaminated with DU either in the form of imbedded shrapnel or inhalation of uranium contaminating dust. The studies of the U.S. armed forces Research Institute in Bethesda Maryland on the shrapnel wounded veteran's demonstrated increased concentration of the isotopes of DU in the urine eight years after the Persian Gulf War. In contrast non-governmental uranium research groups such as Uranium Medical Centre reported increased urinary excretion of four isotopes of DU in the Allied forces veterans exposed to DU containing dust ten years after the exposure. These studies were confirmed by two methods. Neutron activation analysis confirmed presence of DU in the urine of seven Persian Gulf veterans with ratios significantly different from the natural uranium and in the range of DU, ten years after exposure from inhalation. The veterans of the Allied forces contaminated by inhalation in the Persian Gulf War were also analyzed for the uranium presence for their body fluids, tissues and urine by the method of mass spectrometry. These results presented at the International Conferences in Dublin Ireland, Paris France and New York U.S.A. indicate significant presence of four uranium isotopes in over 60% of contaminated veterans being in the range of DU. The ratio of the uranium isotopes 235/238 is in the range of DU if higher than 137.8. It was found to be in the DU ratio 62% examined by the mass spectrometry analysis. Isotopic composition of natural enriched and DU should be for U 238 /99.3, U 235 /0.7 and U 234 /0.006 and for enriched uranium 99.01, 2.96 and 0.03, while for DU respective ratios are 99.75, 0.25 and 0

Continued studies of long-term ecological effects of exposure to uranium

Energy Technology Data Exchange (ETDEWEB)

Hanson, W.C.; Miera, F.R. Jr.

1977-06-01

Studies of the long-term consequences of exposing terrestrial ecosystems to natural and depleted uranium dispersed during explosives tests at Los Alamos Scientific Laboratory (LASL) and test firing at Eglin Air Force Base (EAFB), Florida, were continued. Soils from EAFB, sampled before and after firing of depleted uranium penetrators against armor plate targets, indicated that the upper (0- to 5-cm-deep) soil usually contained more uranium than lower (5- to 10-cm-deep) soil. However, no significant changes were apparent in samples taken before and after the test firing. E-F explosive testing site at LASL was selected for intensive study of uranium redistribution during its 33-yr use. Highest surface soil (0- to 2.5-cm-deep) uranium concentrations occurred 0 and 10 m from the detonation point and averaged 4500 ppM. Concentrations in surface soil 50 and 200 m from the firing point were usually < 15% of that value. The uranium distribution to 30-cm depths showed significant penetration into the soil. Alluvium collected 250 m from the E-F detonation area in Potrillo Canyon indicated that surface (0- to 2.5-cm-deep) uranium concentrations were about 10% of those at the detonation point, and at 2.8 km they were twice background levels.

Environmental radiation monitoring plan for depleted uranium and beryllium areas, Yuma Proving Ground

International Nuclear Information System (INIS)

Ebinger, M.H.; Hansen, W.R.

1994-01-01

This Environmental Radiation Monitoring Plan (ERM) discusses sampling soils, vegetation, and biota for depleted uranium (DU) and beryllium (Be) at Yuma Proving Ground (YPG). The existing ERM plan was used and modified to more adequately assess the potential of DU and Be migration through the YPG ecosystem. The potential pathways for DU and Be migration are discussed and include soil to vegetation, soil to animals, vegetation to animals, animals to animals, and animals to man. Sample collection will show DU deposition and will be used to estimate DU migration. The number of samples from each area varies and depends on if the firing range of interest is currently used for DU testing (GP 17A) or if the range is not used currently for DU testing (GP 20). Twenty to thirty-five individual mammals or lizards will be sampled from each transect. Air samples and samples of dust in the air fall will be collected in three locations in the active ranges. Thirty to forty-five sediment samples will be collected from different locations in the arroys near the impact areas. DU and Be sampling in the Hard Impact and Soft Impact areas changed only slightly from the existing ERM. The modifications are changes in sample locations, addition of two sediment transport locations, addition of vegetation samples, mammal samples, and air sampling from three to five positions on the impact areas. Analysis of samples for DU or total U by inductively-coupled mass spectroscopy (ICP/MS), cc spectroscopy, neutron activation analysis (NAA), and kinetic phosphorimetric analysis (KPA) are discussed, and analysis for Be by ICP/MS are recommended. Acquiring total U (no isotope data) from a large number of samples and analysis of those samples with relatively high total U concentrations results in fewer isotopic identifications but more information on U distribution. From previous studies, total U concentrations greater than about 3 times natural background are usually DU by isotopic confirmation

Effect of niobium element on the electrochemical corrosion behavior of depleted uranium

Energy Technology Data Exchange (ETDEWEB)

Wu, Yanping, E-mail: wuyanping-2@126.com; Wu, Quanwen; Zhu, Shengfa, E-mail: zhushf-306@163.com; Pu, Zhen; Zhang, Yanzhi; Wang, Qinguo; Lang, Dingmu; Zhang, Yuping

2016-09-15

Depleted uranium (DU) has many military and civilian uses. However, its high chemical reactivity limits its application. The effect of Nb content on corrosion behavior of DU is evaluated by scanning Kelvin probe and electrochemical corrosion measurements. The Volta potential value of DU and U-2.5 wt% Nb is about the same level, the Volta potential value of U-5.7 wt% Nb has a rise of 370mV{sub SHE} in comparison with DU. The polarization current of U-5.7 wt% Nb alloy is about an order of magnitude of that of DU. The Nb{sub 2}O{sub 5} is the protective layer for the U-Nb alloys. The negative potential of Nb-depleted α phase is the main reason of the poor corrosion resistance of DU and U-2.5 wt% Nb alloy. - Highlights: • New method (scanning Kelvin probe) was used to study the corrosion property. • Three types of corrosion morphologies were found after potentiodynamic polarization. • The effect of impurity elements on corrosion property was mentioned. • The corrosion mechanism of DU and U-Nb alloys was discussed.

An integrated colloid fractionation approach applied to the characterisation of porewater uranium-humic interactions at a depleted uranium contaminated site

International Nuclear Information System (INIS)

Graham, Margaret C.; Oliver, Ian W.; MacKenzie, Angus B.; Ellam, Robert M.; Farmer, John G.

2008-01-01

Methods for the fractionation of aquatic colloids require careful application to ensure efficient, accurate and reproducible separations. This paper describes the novel combination of mild colloidal fractionation and characterisation methods, namely centrifugal ultrafiltration, gel electrophoresis and gel filtration along with spectroscopic (UV-visible) and elemental (Inductively Coupled Plasma-Optical Emission Spectroscopy, Inductively Coupled Plasma-Mass Spectrometry) analysis, an approach which produced highly consistent results, providing improved confidence in these methods. Application to the study of the colloidal and dissolved components of soil porewaters from one soil at a depleted uranium (DU)-contaminated site revealed uranium (U) associations with both large (100 kDa-0.2 μm) and small (3-30 kDa) humic colloids. For a nearby soil with lower organic matter content, however, association with large (100 kDa-0.2 μm) iron (Fe)-aluminium (Al) colloids in addition to an association with small (3-30 kDa) humic colloids was observed. The integrated colloid fractionation approach presented herein can now be applied with confidence to investigate U and indeed other trace metal migration in soil and aquatic systems

Characterization of Blistering and Delamination in Depleted Uranium Hohlraums

Energy Technology Data Exchange (ETDEWEB)

Biobaum, K. J. M.

2013-03-01

Blistering and delamination are the primary failure mechanisms during the processing of depleted uranium (DU) hohlraums. These hohlraums consist of a sputter-deposited DU layer sandwiched between two sputter-deposited layers of gold; a final thick gold layer is electrodeposited on the exterior. The hohlraum is deposited on a copper-coated aluminum mandrel; the Al and Cu are removed with chemical etching after the gold and DU layers are deposited. After the mandrel is removed, blistering and delamination are observed on the interiors of some hohlraums, particularly at the radius region. It is hypothesized that blisters are caused by pinholes in the copper and gold layers; etchant leaking through these holes reaches the DU layer and causes it to oxidize, resulting in a blister. Depending on the residual stress in the deposited layers, blistering can initiate larger-scale delamination at layer interfaces. Scanning electron microscopy indicates that inhomogeneities in the machined aluminum mandrel are replicated in the sputter-deposited copper layer. Furthermore, the Cu layer exhibits columnar growth with pinholes that likely allow etchant to come in contact with the gold layer. Any inhomogeneities or pinholes in this initial gold layer then become nucleation sites for blistering. Using a focused ion beam system to etch through the gold layer and extract a cross-sectional sample for transmission electron microscopy, amorphous, intermixed layers at the gold/DU interfaces are observed. Nanometer-sized bubbles in the sputtered and electrodeposited gold layers are also present. Characterization of the morphology and composition of the deposited layers is the first step in determining modifications to processing parameters, with the goal of attaining a significant improvement in hohlraum yield.

Cost Analysis of Remediation Systems for Depleted Uranium

Science.gov (United States)

2014-04-01

radioactive metal in all rocks and soils. There are three existing uranium isotopes, and all three are radioactive and emit decay products upon...the chemical toxicity of soluble forms of uranium . If internalized, uranium will cause health problems, as is the case with other heavy metals such...blunt mushroom shape as it penetrates armor, which limits its effectiveness. With a density of 17.6 g/cm3 it weighs less than DU. Uranium oxidizes

Potential behavior of depleted uranium penetrators under shipping and bulk storage accident conditions

Energy Technology Data Exchange (ETDEWEB)

Mishima, J.; Parkhurst, M.A.; Scherpelz, R.I.

1985-03-01

An investigation of the potential hazard from airborne releases of depleted uranium (DU) from the Army's M829 munitions was conducted at the Pacific Northwest Laboratory. The study included: (1) assessing the characteristics of DU oxide from an April 1983 burn test, (2) postulating conditions of specific accident situations, and (3) reviewing laboratory and theoretical studies of oxidation and airborne transport of DU from accidents. Results of the experimental measurements of the DU oxides were combined with atmospheric transport models and lung and kidney exposure data to help establish reasonable exclusion boundaries to protect personnel and the public at an accident site. 121 references, 44 figures, 30 tables.

Potential benefits and impacts on the CRWMS transportation system of filling spent fuel shipping casks with depleted uranium silicate glass

International Nuclear Information System (INIS)

Pope, R.B.; Forsberg, C.W.; DeHart, M.D.; Childs, K.W.; Tang, J.S.

1996-01-01

A new technology, the Depleted Uranium Silicate COntainer Fill System (DUSCOFS), is proposed to improve the performance and reduce the uncertainties of geological disposal of spent nuclear fuel (SNF), thus reducing both radionuclide release rates from the waste package and the potential for repository nuclear criticality events. DUSCOFS may also provide benefits for SNF storage and transport if it is loaded into the container early in the waste management cycle. Assessments have been made of the benefits to be derived by placing depleted uranium silicate (DUS) glass into SNF containers for enhancing repository performance assessment and controlling criticality over geologic times in the repository. Also, the performance, benefits, and impacts which can be derived if the SNF is loaded into a multi-purpose canister with DUS glass at a reactor site have been assessed. The DUSCOFS concept and the benefits to the waste management cycle of implementing DUSCOFS early in the cycle are discussed in this paper

Geological-economic analysis on the exploration of backup resources for depleted mines in Lujing uranium ore-field, central-southern China

International Nuclear Information System (INIS)

Li Deping; Wang Zhicheng; Fan Shaoyun

2006-01-01

With the geological-economic evaluation program for pithead heap-leaching mining uranium deposits developed by the authors and the data of column-leaching tests and the geological reserve, the geological-economic evaluation is made to the residual geological reserves of both Lujing and Huangfengling deposit, and the geological reserves of Yangjiaonao deposit of the depleted mines in Lujing uranium ore-field, central-southern China. The results of static analysis on these reserves show that the residual geological reserves of both Lujing and Huangfengling deposit belong to sub-profitable type, but the ones of Yangjiaonao deposit is profitable with 26.56% tax-before profit. 1 tU profitable type of ore from Yangjiaonao deposit can use 2.40-3.79 tU subprofitable type of ores from Lujing and Huangfengling deposit. In order to solving the problem on scarcity of backup resources of the depleted mines in Lujing uranium ore-field and using the existing sub-profitable type of geological reserves, it is suggested that the high grade of profitable type of deposits should be explored around the exhausting mines so that the production of the mines could be profitable by the pithead heap-leaching mining method with arrangement groups of both sub-profitable and profitable type of ores. (authors)

The U.S. Department of Veterans' Affairs depleted uranium exposed cohort at 25 Years: Longitudinal surveillance results

Energy Technology Data Exchange (ETDEWEB)

McDiarmid, Melissa A.; Gaitens, Joanna M.; Hines, Stella [Department of Veterans Affairs Medical Center Baltimore, Maryland, 10 N. Greene St., Baltimore, MD 21201 (United States); Department of Medicine, University of Maryland School of Medicine, 655 W Baltimore S, Baltimore, MD 21201 (United States); Condon, Marian, E-mail: mcondon@medicine.umaryland.edu [Department of Veterans Affairs Medical Center Baltimore, Maryland, 10 N. Greene St., Baltimore, MD 21201 (United States); Roth, Tracy; Oliver, Marc; Gucer, Patricia [Department of Veterans Affairs Medical Center Baltimore, Maryland, 10 N. Greene St., Baltimore, MD 21201 (United States); Department of Medicine, University of Maryland School of Medicine, 655 W Baltimore S, Baltimore, MD 21201 (United States); Brown, Lawrence [Department of Veterans Affairs Medical Center Baltimore, Maryland, 10 N. Greene St., Baltimore, MD 21201 (United States); Department of Pathology, University of Maryland School of Medicine, 655 W Baltimore S, Baltimore, MD 21201 (United States); Centeno, Jose A. [US Food and Drug Administration, Center for Devices and Radiological Health Office of Science and Engineering Laboratories, Silver Spring, MD 20993 (United States); Dux, Moira [Department of Veterans Affairs Medical Center Baltimore, Maryland, 10 N. Greene St., Baltimore, MD 21201 (United States); Squibb, Katherine S. [Department of Veterans Affairs Medical Center Baltimore, Maryland, 10 N. Greene St., Baltimore, MD 21201 (United States); Department of Medicine, University of Maryland School of Medicine, 655 W Baltimore S, Baltimore, MD 21201 (United States)

2017-01-15

Background: A small group of Gulf War I veterans wounded in depleted uranium (DU) friendly-fire incidents have been monitored for health changes in a clinical surveillance program at the Veterans Affairs Medical Center, Baltimore since 1994. Methods: During the spring of 2015, an in-patient clinical surveillance protocol was performed on 36 members of the cohort, including exposure monitoring for total and isotopic uranium concentrations in urine and a comprehensive assessment of health outcomes. Results: On-going mobilization of U from embedded fragments is evidenced by elevated urine U concentrations. The DU isotopic signature is observed principally in participants possessing embedded fragments. Those with only an inhalation exposure have lower urine U concentration and a natural isotopic signature. Conclusions: At 25 years since first exposure to DU, an aging cohort of military veterans continues to show no U-related health effects in known target organs of U toxicity. As U body burden continues to accrue from in-situ mobilization from metal fragment depots, and increases with exposure duration, critical tissue-specific U concentration thresholds may be reached, thus recommending on-going surveillance of this veteran cohort. - Highlights: • Gulf War I veterans wounded with depleted uranium are monitored for health changes. • In 2015 in-patient clinical surveillance was performed on 36 members of the cohort. • Mobilization of U from embedded fragments is evidenced by elevated U in urine. • This cohort of continues to show no U-related health effects.

The U.S. Department of Veterans' Affairs depleted uranium exposed cohort at 25 Years: Longitudinal surveillance results

International Nuclear Information System (INIS)

McDiarmid, Melissa A.; Gaitens, Joanna M.; Hines, Stella; Condon, Marian; Roth, Tracy; Oliver, Marc; Gucer, Patricia; Brown, Lawrence; Centeno, Jose A.; Dux, Moira; Squibb, Katherine S.

2017-01-01

Background: A small group of Gulf War I veterans wounded in depleted uranium (DU) friendly-fire incidents have been monitored for health changes in a clinical surveillance program at the Veterans Affairs Medical Center, Baltimore since 1994. Methods: During the spring of 2015, an in-patient clinical surveillance protocol was performed on 36 members of the cohort, including exposure monitoring for total and isotopic uranium concentrations in urine and a comprehensive assessment of health outcomes. Results: On-going mobilization of U from embedded fragments is evidenced by elevated urine U concentrations. The DU isotopic signature is observed principally in participants possessing embedded fragments. Those with only an inhalation exposure have lower urine U concentration and a natural isotopic signature. Conclusions: At 25 years since first exposure to DU, an aging cohort of military veterans continues to show no U-related health effects in known target organs of U toxicity. As U body burden continues to accrue from in-situ mobilization from metal fragment depots, and increases with exposure duration, critical tissue-specific U concentration thresholds may be reached, thus recommending on-going surveillance of this veteran cohort. - Highlights: • Gulf War I veterans wounded with depleted uranium are monitored for health changes. • In 2015 in-patient clinical surveillance was performed on 36 members of the cohort. • Mobilization of U from embedded fragments is evidenced by elevated U in urine. • This cohort of continues to show no U-related health effects.

Estimation of uranium in bioassay samples of occupational workers by laser fluorimetry

International Nuclear Information System (INIS)

Suja, A.; Prabhu, S.P.; Sawant, P.D.; Sarkar, P.K.; Tiwari, A.K.; Sharma, R.

2010-01-01

A newly established uranium processing facility has been commissioned at BARC, Trombay. Monitoring of occupational workers at regulars intervals is essential to assess intake of uranium by the workers in this facility. The design and engineering safety features of the plant are such that there is very low probability of uranium getting air borne during normal operations. However, the leakages from the system during routine maintenance of the plant may result in intake of uranium by workers. As per the new biokinetic model for uranium, 63% of uranium entering the blood stream gets directly excreted in urine. Therefore, bioassay monitoring (urinalysis) was recommended for these workers. A group of 21 workers was selected for bioassay monitoring to assess the existing urinary excretion levels of uranium before the commencement of actual work. For this purpose, sample collection kit along with an instruction slip was provided to the workers. Bioassay samples received were wet ashed with conc. nitric acid and hydrogen peroxide to break down the metabolized complexes of uranium and it was co-precipitated with calcium phosphate. Separation of uranium from the matrix was done using ion exchange technique and final activity quantification in these samples was done using laser fluorimeter (Quantalase, Model No. NFL/02). Calibration of the laser fluorimeter is done using 10 ppb uranium standard (WHO, France Ref. No. 180000). Verification of the system performance is done by measuring concentration of uranium in the standards (1 ppb to 100 ppb). Standard addition method was followed for estimation of uranium concentration in the samples. Uranyl ions present in the sample get excited by pulsed nitrogen laser at 337.1 nm, and on de-excitation emit fluorescence light (540 nm) intensity which is measured by the PMT. To estimate the uranium in the bioassay samples, a known aliquot of the sample was mixed with 5% sodium pyrophosphate and fluorescence intensity was measured

Medical effects of internal contamination with uranium.

Science.gov (United States)

Duraković, A

1999-03-01

The purpose of this work is to present an outline of the metabolic pathways of uranium isotopes and compounds, medical consequences of uranium poisoning, and an evaluation of the therapeutic alternatives in uranium internal contamination. The chemical toxicity of uranium has been recognized for more than two centuries. Animal experiments and human studies are conclusive about metabolic adverse affects and nephro- toxicity of uranium compounds. Radiation toxicity of uranium isotopes has been recognized since the beginning of the nuclear era, with well documented evidence of reproductive and developmental toxicity, as well as mutagenic and carcinogenic consequences of uranium internal contamination. Natural uranium (238U), an alpha emitter with a half-life of 4.5x10(9) years, is one of the primordial substances of the universe. It is found in the earth's crust, combined with 235U and 234U, alpha, beta, and gamma emitters with respective half-lives of 7.1x10(8) and 2.5x10(5) years. A special emphasis of this paper concerns depleted uranium. The legacy of radioactive waste, environmental and health hazards in the nuclear industry, and, more recently, the military use of depleted uranium in the tactical battlefield necessitates further insight into the toxicology of depleted uranium. The present controversy over the radiological and chemical toxicity of depleted uranium used in the Gulf War warrants further experimental and clinical investigations of its effects on the biosphere and human organisms.

Filtration system for the removal of depleted uranium from water

International Nuclear Information System (INIS)

Barlett, P.T.; Wolfe, S.

1989-01-01

Previous depleted uranium (DU) munitions testing has resulted in 2 132 cubic meters (500 to 35,000 gallons) of wastewater containing: DU concentrations from 2.5 x 10 -5 to 9 x 10 -8 microcuries/mL DU particles equal to and greater than 0.1 micron in size. Personnel reasoned that if particles could be filtered from the wastewater down to a 0.1 micron size, the wastewater could be disposed of on-site and comply with the Nuclear Regulatory Commission (NRC) standard of 35 pCi/g of soil. This paper compares the effectiveness of three cross-flow membrane modules using a pilot-scale microfiltration (MF) system that was designed to process the wastewater described and designed to allow direct scale-up to a system that is capable of processing 132 m 3 (35,000 gals) of wastewater that can then be disposed of on-site within applicable standards. A cross-flow MF system was designed, assembled, and tested using replicated wastewater

The use of depleted uranium ammunition during NATO aggression against Federal Republic of Yugoslavia

International Nuclear Information System (INIS)

Zaric, M.; Petkovic, S.; Devic, Z.

2002-01-01

It is well known that DU (depleted uranium) weaponry was extensively used during the 'Desert Storm' operation in Iraq. There is no doubt that NATO used DU ammunition in Bosnia in 1994 and 1995. It is also common knowledge that many NATO armies are equipped with DU ammunition in various calibers (from 20 up to 155 mm) as a standard part of certain weapon systems. These facts, as a result of literature research, as well as Yugoslav Army (YA) intelligence data on the eve of the aggression clearly showed that NATO most probably would use DU ammunition. (author)

Depleted and enriched uranium exposure quantified in former factory workers and local residents of NL Industries, Colonie, NY USA

International Nuclear Information System (INIS)

Arnason, John G.; Pellegri, Christine N.; Moore, June L.; Lewis-Michl, Elizabeth L.; Parsons, Patrick J.

2016-01-01

Background: Between 1958 and 1982, NL Industries manufactured components of enriched (EU) and depleted uranium (DU) at a factory in Colonie NY, USA. More than 5 metric tons of DU was deposited as microscopic DU oxide particles on the plant site and surrounding residential community. A prior study involving a small number of individuals (n=23) indicated some residents were exposed to DU and former workers to both DU and EU, most probably through inhalation of aerosol particles. Objectives: Our aim was to measure total uranium [U] and the uranium isotope ratios: 234 U/ 238 U; 235 U/ 238 U; and 236 U/ 238 U, in the urine of a cohort of former workers and nearby residents of the NLI factory, to characterize individual exposure to natural uranium (NU), DU, and EU more than 3 decades after production ceased. Methods: We conducted a biomonitoring study in a larger cohort of 32 former workers and 99 residents, who may have been exposed during its period of operation, by measuring Total U, NU, DU, and EU in urine using Sector Field Inductively Coupled Plasma - Mass Spectrometry (SF-ICP-MS). Results: Among workers, 84% were exposed to DU, 9% to EU and DU, and 6% to natural uranium (NU) only. For those exposed to DU, urinary isotopic and [U] compositions result from binary mixing of NU and the DU plant feedstock. Among residents, 8% show evidence of DU exposure, whereas none shows evidence of EU exposure. For residents, the [U] geometric mean is significantly below the value reported for NHANES. There is no significant difference in [U] between exposed and unexposed residents, suggesting that [U] alone is not a reliable indicator of exposure to DU in this group. Conclusions: Ninety four percent of workers tested showed evidence of exposure to DU, EU or both, and were still excreting DU and EU decades after leaving the workforce. The study demonstrates the advantage of measuring multiple isotopic ratios (e.g., 236 U/ 238 U and 235 U/ 238 U) over a single ratio ( 235 U/ 238 U

Uranium determination in soil samples using Eichrom resins

International Nuclear Information System (INIS)

Marabini, S.; Serdeiro, Nelidad H.

2003-01-01

Traditionally, the radiochemical methods for uranium activity determination in soil samples by alpha spectrometry, use some techniques like solvent extraction, precipitation and ion exchange in the separation and purification stages. In the last years, some new materials have been developed for using in extraction chromatography, specific for actinides determinations. In the present method the long and tedious stages were eliminated, and the reagents consumption and concentration were minimised. This new procedure was applied to soils since it is one of the most complex matrices. In order to reduce time and chemical reagents, the soil samples up to 0,5 g were leached with nitric, hydrofluoric and perchloric acids in hermetic sealed recipients of Teflon at 150 C degrees during 5 hours. UTEVA Eichrom resin was used for uranium separation and purification. The uranium activity concentration was determined by alpha spectrometry. Several standard samples were analysed and the results are presented. (author)

Determination of uranium and its isotopic ratios in environmental samples

International Nuclear Information System (INIS)

Flues Szeles, M.S.M.

1990-01-01

A method for the determination of uranium and its isotopic ratios ( sup(235)U/ sup(238)U and sup(234U/ sup(238)U) is established in the present work. The method can be applied in environmental monitoring programs of uranium enrichment facilities. The proposed method is based on the alpha spectrometry technique which is applied after a purification of the sample by using an ionic exchange resin. The total yield achieved was (91 + 5)% with a precision of 5%, an accuracy of 8% and a lower limit of detection of 7,9 x 10 sup(-4)Bq. The uranium determination in samples containing high concentration of iron, which is an interfering element present in environmental samples, particularly in soil and sediment, was also studied. The results obtained by using artificial samples containing iron and uranium in the ratio 1000:1, were considered satisfactory. (author)

Bioaccumulation and biological effects in the earthworm Eisenia fetida exposed to natural and depleted uranium

Energy Technology Data Exchange (ETDEWEB)

Giovanetti, Anna, E-mail: anna.giovanetti@enea.i [ENEA, Institute of Radiation Protection, CR Casaccia Via Anguillarese 301, 00123 Rome (Italy); Fesenko, Sergey [International Atomic Energy Agency (IAEA), Agency' s Laboratories Seibersdorf, A-2444 Seibersdorf (Austria); Cozzella, Maria L. [ENEA, National Institute for Metrology of Ionizing Radiation, CR Casaccia Via Anguillarese 301, 00123 Rome (Italy); Asencio, Lisbet D. [Centro de Estudios Ambientales, Carretera a Castillo de Jagua, CP. 59350 C. Nuclear, Cienfuegos (Cuba); Sansone, Umberto [International Atomic Energy Agency (IAEA), Agency' s Laboratories Seibersdorf, A-2444 Seibersdorf (Austria)

2010-06-15

The accumulations of both natural (U) and depleted (DU) uranium in the earthworms (Eisenia fetida) were studied to evaluate corresponding biological effects. Concentrations of metals in the experimental soil ranged from 1.86 to 600 mg kg{sup -1}. Five biological endpoints: mortality, animals' weight increasing, lysosomal membrane stability by measuring the neutral red retention time (the NRRT), histological changes and genetic effects (Comet assay) were used to evaluate biological effects in the earthworms after 7 and 28 days of exposure. No effects have been observed in terms of mortality or weight reduction. Cytotoxic and genetic effects were identified at quite low U concentrations. For some of these endpoints, in particular for genetic effects, the dose (U concentration)-effect relationships have been found to be non-linear. The results have also shown a statistically significant higher level of impact on the earthworms exposed to natural U compared to depleted U.

Bioaccumulation and biological effects in the earthworm Eisenia fetida exposed to natural and depleted uranium

International Nuclear Information System (INIS)

Giovanetti, Anna; Fesenko, Sergey; Cozzella, Maria L.; Asencio, Lisbet D.; Sansone, Umberto

2010-01-01

The accumulations of both natural (U) and depleted (DU) uranium in the earthworms (Eisenia fetida) were studied to evaluate corresponding biological effects. Concentrations of metals in the experimental soil ranged from 1.86 to 600 mg kg -1 . Five biological endpoints: mortality, animals' weight increasing, lysosomal membrane stability by measuring the neutral red retention time (the NRRT), histological changes and genetic effects (Comet assay) were used to evaluate biological effects in the earthworms after 7 and 28 days of exposure. No effects have been observed in terms of mortality or weight reduction. Cytotoxic and genetic effects were identified at quite low U concentrations. For some of these endpoints, in particular for genetic effects, the dose (U concentration)-effect relationships have been found to be non-linear. The results have also shown a statistically significant higher level of impact on the earthworms exposed to natural U compared to depleted U.

Uranium bioaccumulation and biological disorders induced in zebrafish (Danio rerio) after a depleted uranium waterborne exposure

Energy Technology Data Exchange (ETDEWEB)

Barillet, Sabrina, E-mail: sabrina.barillet@free.f [Laboratory of Radioecology and Ecotoxicology, IRSN (Institute for Radiological protection and Nuclear Safety), DEI/SECRE/LRE, Cadarache, Bat 186, BP 3, 13115 St-Paul-Lez-Durance cedex (France); Adam-Guillermin, Christelle, E-mail: christelle.adam-guillermin@irsn.f [Laboratory of Radioecology and Ecotoxicology, IRSN (Institute for Radiological protection and Nuclear Safety), DEI/SECRE/LRE, Cadarache, Bat 186, BP 3, 13115 St-Paul-Lez-Durance cedex (France); Palluel, Olivier, E-mail: olivier.palluel@ineris.f [Ecotoxicological Risk Assessment Unit, INERIS (National Institute for Industrial Environment and Risks), Parc technologique ALATA, 60 550 Verneuil-en-Halatte (France); Porcher, Jean-Marc, E-mail: jean-marc.porcher@ineris.f [Ecotoxicological Risk Assessment Unit, INERIS (National Institute for Industrial Environment and Risks), Parc technologique ALATA, 60 550 Verneuil-en-Halatte (France); Devaux, Alain, E-mail: alain.devaux@entpe.f [Universite de Lyon, INRA, EFPA-SA, Environmental Science Laboratory (LSE), ENTPE, 69518 Vaulx en Velin cedex (France)

2011-02-15

Because of its toxicity and its ubiquity within aquatic compartments, uranium (U) represents a significant hazard to aquatic species such as fish. In a previous study, we investigated some biological responses in zebrafish either exposed to depleted or to enriched U (i.e., to different radiological activities). However, results required further experiments to better understand biological responses. Moreover, we failed to clearly demonstrate a significant relationship between biological effects and U radiological activity. We therefore chose to herein examine U bioaccumulation and induced effects in zebrafish according to a chemical dose-response approach. Results showed that U is highly bioconcentrated in fish, according to a time- and concentration-dependent model. Additionally, hepatic antioxidant defenses, red blood cells DNA integrity and brain acetylcholinesterase activity were found to be significantly altered. Generally, the higher the U concentration, the sooner and/or the greater the effect, suggesting a close relationship between accumulation and effect. - Research highlights: Depleted U bioconcentration factor is of about 1000 in zebrafish exposed to 20 {mu}g/L. Hepatic antioxidant disorders are noticed as soon as the first hours of exposure. DNA damage is induced in red blood cells after 20 d of exposure to 500 {mu}g DU/L. The brain cholinergic system (AChE activity) is impacted. - This study demonstrates that U is highly bioaccumulated in fish, resulting in biological disorders such as hepatic oxidative stress as well as genotoxic and neurotoxic events.

Uranium bioaccumulation and biological disorders induced in zebrafish (Danio rerio) after a depleted uranium waterborne exposure

International Nuclear Information System (INIS)

Barillet, Sabrina; Adam-Guillermin, Christelle; Palluel, Olivier; Porcher, Jean-Marc; Devaux, Alain

2011-01-01

Because of its toxicity and its ubiquity within aquatic compartments, uranium (U) represents a significant hazard to aquatic species such as fish. In a previous study, we investigated some biological responses in zebrafish either exposed to depleted or to enriched U (i.e., to different radiological activities). However, results required further experiments to better understand biological responses. Moreover, we failed to clearly demonstrate a significant relationship between biological effects and U radiological activity. We therefore chose to herein examine U bioaccumulation and induced effects in zebrafish according to a chemical dose-response approach. Results showed that U is highly bioconcentrated in fish, according to a time- and concentration-dependent model. Additionally, hepatic antioxidant defenses, red blood cells DNA integrity and brain acetylcholinesterase activity were found to be significantly altered. Generally, the higher the U concentration, the sooner and/or the greater the effect, suggesting a close relationship between accumulation and effect. - Research highlights: → Depleted U bioconcentration factor is of about 1000 in zebrafish exposed to 20 μg/L. → Hepatic antioxidant disorders are noticed as soon as the first hours of exposure. → DNA damage is induced in red blood cells after 20 d of exposure to 500 μg DU/L. → The brain cholinergic system (AChE activity) is impacted. - This study demonstrates that U is highly bioaccumulated in fish, resulting in biological disorders such as hepatic oxidative stress as well as genotoxic and neurotoxic events.

Assessing the Renal Toxicity of Capstone Depleted Uranium Oxides and Other Uranium Compounds

International Nuclear Information System (INIS)

Roszell, Laurie E.; Hahn, Fletcher; Lee, Robyn B.; Parkhurst, MaryAnn

2009-01-01

The primary target for uranium toxicity is the kidney. The most frequently used guideline for uranium kidney burdens is the International Commission on Radiation Protection (ICRP) value of 3 (micro)g U/g kidney, a value that is based largely upon chronic studies in animals. In the present effort, we have developed a risk model equation to assess potential outcomes of acute uranium exposure. Twenty-seven previously published case studies in which workers were acutely exposed to soluble compounds of uranium (as a result of workplace accidents) were analyzed. Kidney burdens of uranium for these individuals were determined based on uranium in the urine, and correlated with health effects observed over a period of up to 38 years. Based upon the severity of health effects, each individual was assigned a score (- to +++) and then placed into an Effect Group. A discriminant analysis was used to build a model equation to predict the Effect Group based on the amount of uranium in the kidneys. The model equation was able to predict the Effect Group with 85% accuracy. The risk model was used to predict the Effect Group for Soldiers exposed to DU as a result of friendly fire incidents during the 1991 Gulf War. This model equation can also be used to predict the Effect Group of new cases in which acute exposures to uranium have occurred

Characterisation and dissolution of depleted uranium aerosols produced during impacts of kinetic energy penetrators against a tank

International Nuclear Information System (INIS)

Chazel, V.; Gerasimo, P.; Debouis, V.; Laroche, P.; Paquet, F.

2003-01-01

Aerosols produced during impacts of depleted uranium (DU) penetrators against the glacis (sloping armour) and the turret of a tank were sampled. The concentration and size distribution were determined. Activity median aerodynamic diameters were 1 μm (geometric standard deviation, s g = 3.7) and 2 μm (s g = 2.5), respectively, for glacis and turret. The mean air concentration was 120 Bq m -3 , i.e. 8.5 mg m -3 of DU. Filters analysed by scanning electron microscopy (SEM) and X ray diffraction showed two types of particles (fine particles and large molten particles) composed mainly of a mixture of uranium and aluminium. The uranium oxides were mostly U 3 O 8 , UO 2.25 and probably UO 3.01 and a mixed compound of U and Al. The kinetics of dissolution in three media (HCO 3 - , HCl and Gamble's solution) were determined using in-vitro tests. The slow dissolution rates were respectively slow, and intermediate between slow and moderate, and the rapid dissolution fractions were mostly intermediate between moderate and fast. According to the in-vitro results for Gamble's solution, and based on a hypothetical single acute inhalation of 90 Bq, effective doses integrated up to 1 y after incorporation were 0.54 and 0.56 mSv respectively, for aerosols from glacis and turret. In comparison, the ICRP limits are 20 mSv y -1 for workers and 1 mSv y -1 for members of public. A kidney concentration of approximately 0.1 μg U g -1 was predicted and should not, in this case, lead to kidney damage. (author)

Characterisation and dissolution of depleted uranium aerosols produced during impacts of kinetic energy penetrators against a tank.

Science.gov (United States)

Chazel, V; Gerasimo, P; Dabouis, V; Laroche, P; Paquet, F

2003-01-01

Aerosols produced during impacts of depleted uranium (DU) penetrators against the glacis (sloping armour) and the turret of a tank were sampled. The concentration and size distribution were determined. Activity median aerodynamic diameters were 1 microm (geometric standard deviation, sigma(g) = 3.7) and 2 microm (sigma(g) = 2.5), respectively, for glacis and turret. The mean air concentration was 120 Bq m(-3), i.e. 8.5 mg m(-3) of DU. Filters analysed by scanning electron microscopy (SEM) and X ray diffraction showed two types of particles (fine particles and large molten particles) composed mainly of a mixture of uranium and aluminium. The uranium oxides were mostly U3O8, UO2.25 and probably UO3.01 and a mixed compound of U and Al. The kinetics of dissolution in three media (HCO3-, HCl and Gamble's solution) were determined using in-vitro tests. The slow dissolution rates were respectively slow, and intermediate between slow and moderate, and the rapid dissolution fractions were mostly intermediate between moderate and fast. According to the in-vitro results for Gamble's solution, and based on a hypothetical single acute inhalation of 90 Bq, effective doses integrated up to 1 y after incorporation were 0.54 and 0.56 mSv, respectively, for aerosols from glacis and turret. In comparison, the ICRP limits are 20 mSv y(-1) for workers and 1 mSv y(-1) for members of the public. A kidney concentration of approximately 0.1 microg U g(-1) was predicted and should not, in this case, lead to kidney damage.

Radiochronological Age of a Uranium Metal Sample from an Abandoned Facility

Energy Technology Data Exchange (ETDEWEB)

Meyers, L A; Williams, R W; Glover, S E; LaMont, S P; Stalcup, A M; Spitz, H B

2012-03-16

A piece of scrap uranium metal bar buried in the dirt floor of an old, abandoned metal rolling mill was analyzed using multi-collector inductively coupled plasma mass spectroscopy (MC-ICP-MS). The mill rolled uranium rods in the 1940s and 1950s. Samples of the contaminated dirt in which the bar was buried were also analyzed. The isotopic composition of uranium in the bar and dirt samples were both the same as natural uranium, though a few samples of dirt also contained recycled uranium; likely a result of contamination with other material rolled at the mill. The time elapsed since the uranium metal bar was last purified can be determined by the in-growth of the isotope {sup 230}Th from the decay of {sup 234}U, assuming that only uranium isotopes were present in the bar after purification. The age of the metal bar was determined to be 61 years at the time of this analysis and corresponds to a purification date of July 1950 {+-} 1.5 years.

Radiochronological age of a uranium metal sample from an abandoned facility

International Nuclear Information System (INIS)

Meyers, L.A.; Stalcup, A.M.; Glover, S.E.; Spitz, H.B.

2013-01-01

A piece of scrap uranium metal bar buried in the dirt floor of an old, abandoned metal rolling mill was analyzed using multi-collector inductively coupled plasma mass spectroscopy (MC-ICP-MS). The mill rolled uranium rods in the 1940 and 1950s. Samples of the contaminated dirt in which the bar was buried were also analyzed. The isotopic composition of uranium in the bar and dirt samples were both the same as natural uranium, though a few samples of dirt also contained recycled uranium; likely a result of contamination with other material rolled at the mill. The time elapsed since the uranium metal bar was last purified can be determined by the in-growth of the isotope 230 Th from the decay of 234 U, assuming that only uranium isotopes were present in the bar after purification. The age of the metal bar was determined to be 61 years at the time of this analysis and corresponds to a purification date of July 1950 ± 1.5 years. (author)

Radiochronological Age of a Uranium Metal Sample from an Abandoned Facility

International Nuclear Information System (INIS)

Meyers, L.A.; Williams, R.W.; Glover, S.E.; LaMont, S.P.; Stalcup, A.M.; Spitz, H.B.

2012-01-01

A piece of scrap uranium metal bar buried in the dirt floor of an old, abandoned metal rolling mill was analyzed using multi-collector inductively coupled plasma mass spectroscopy (MC-ICP-MS). The mill rolled uranium rods in the 1940s and 1950s. Samples of the contaminated dirt in which the bar was buried were also analyzed. The isotopic composition of uranium in the bar and dirt samples were both the same as natural uranium, though a few samples of dirt also contained recycled uranium; likely a result of contamination with other material rolled at the mill. The time elapsed since the uranium metal bar was last purified can be determined by the in-growth of the isotope 230 Th from the decay of 234 U, assuming that only uranium isotopes were present in the bar after purification. The age of the metal bar was determined to be 61 years at the time of this analysis and corresponds to a purification date of July 1950 ± 1.5 years.

Short-term hepatic effects of depleted uranium on xenobiotic and bile acid metabolizing cytochrome P450 enzymes in the rat

International Nuclear Information System (INIS)

Gueguen, Y.; Souidi, M.; Baudelin, C.; Dudoignon, N.; Grison, S.; Dublineau, I.; Marquette, C.; Voisin, P.; Gourmelon, P.; Aigueperse, J.

2006-01-01

The toxicity of uranium has been demonstrated in different organs, including the kidneys, skeleton, central nervous system, and liver. However, few works have investigated the biological effects of uranium contamination on important metabolic function in the liver. In vivo studies were conducted to evaluate its effects on cytochrome P450 (CYP) enzymes involved in the metabolism of cholesterol and xenobiotics in the rat liver. The effects of depleted uranium (DU) contamination on Sprague-Dawley were measured at 1 and 3 days after exposure. Biochemical indicators characterizing liver and kidney functions were measured in the plasma. The DU affected bile acid CYP activity: 7α-hydroxycholesterol plasma level decreased by 52% at day 3 whereas microsomal CYP7A1 activity in the liver did not change significantly and mitochondrial CYP27A1 activity quintupled at day 1. Gene expression of the nuclear receptors related to lipid metabolism (FXR and LXR) also changed, while PPARα mRNA levels did not. The increased mRNA levels of the xenobiotic-metabolizing CYP3A enzyme at day 3 may be caused by feedback up-regulation due to the decreased CYP3A activity at day 1. CAR mRNA levels, which tripled on day 1, may be involved in this up-regulation, while mRNA levels of PXR did not change. These results indicate that high levels of depleted uranium, acting through modulation of the CYP enzymes and some of their nuclear receptors, affect the hepatic metabolism of bile acids and xenobiotics. (orig.)

Use of a radioactive substance, the depleted uranium, for the fabrication of enamels and usual things and jewels decoration

International Nuclear Information System (INIS)

1999-01-01

This open letter to the ministers and State Secretaries of the public health, the environment and the consumers protection, deals with a complaint against X, lodged by the CRII-RAD. This complaint concerns the use of depleted uranium for the fabrication of enamels and the decoration of usual things and jewels. This utilization constitutes a breach of the decree 66-450, which forbids since 1966 the addition of radioactive substances in food, cosmetic and domestic products. The letter takes into account the hazards for the workers and the consumers, the uranium powder origin and discusses the guaranties forecast under the legislation eye. (A.L.B.)

Preconceptual design studies and cost data of depleted uranium hexafluoride conversion plants

International Nuclear Information System (INIS)

Jones, E

1999-01-01

One of the more important legacies left with the Department of Energy (DOE) after the privatization of the United States Enrichment Corporation is the large inventory of depleted uranium hexafluoride (DUF6). The DOE Office of Nuclear Energy, Science and Technology (NE) is responsible for the long-term management of some 700,000 metric tons of DUF6 stored at the sites of the two gaseous diffusion plants located at Paducah, Kentucky and Portsmouth, Ohio, and at the East Tennessee Technology Park in Oak Ridge, Tennessee. The DUF6 management program resides in NE's Office of Depleted Uranium Hexafluoride Management. The current DUF6 program has largely focused on the ongoing maintenance of the cylinders containing DUF6. However, the long-term management and eventual disposition of DUF6 is the subject of a Programmatic Environmental Impact Statement (PEIS) and Public Law 105-204. The first step for future use or disposition is to convert the material, which requires construction and long-term operation of one or more conversion plants. To help inform the DUF6 program's planning activities, it was necessary to perform design and cost studies of likely DUF6 conversion plants at the preconceptual level, beyond the PEIS considerations but not as detailed as required for conceptual designs of actual plants. This report contains the final results from such a preconceptual design study project. In this fast track, three month effort, Lawrence Livermore National Laboratory and Bechtel National Incorporated developed and evaluated seven different preconceptual design cases for a single plant. The preconceptual design, schedules, costs, and issues associated with specific DUF6 conversion approaches, operating periods, and ownership options were evaluated based on criteria established by DOE. The single-plant conversion options studied were similar to the dry-conversion process alternatives from the PEIS. For each of the seven cases considered, this report contains information on

Depleted UF6 programmatic environmental impact statement

International Nuclear Information System (INIS)

1997-01-01

The US Department of Energy has developed a program for long-term management and use of depleted uranium hexafluoride, a product of the uranium enrichment process. As part of this effort, DOE is preparing a Programmatic Environmental Impact Statement (PEIS) for the depleted UF 6 management program. This report duplicates the information available at the web site (http://www.ead.anl.gov/web/newduf6) set up as a repository for the PEIS. Options for the web site include: reviewing recent additions or changes to the web site; learning more about depleted UF 6 and the PEIS; browsing the PEIS and related documents, or submitting official comments on the PEIS; downloading all or part of the PEIS documents; and adding or deleting one's name from the depleted UF 6 mailing list

Differences in in vitro dissolution properties of settled and airborne uranium material

International Nuclear Information System (INIS)

Scripsick, R.C.; Crist, K.C.; Tillery, M.I.; Soderholm, S.C.

1984-01-01

The dissolution behavior of settled and airborne uranium material produced by firing of depleted uranium munitions was studied using an in vitro dissolution technique. Differences in the composition of bulk and respirable fraction samples of these materials were observed. Dissolution analysis results suggest that under some conditions a rapidly dissolving uranium fraction may be formed. This fraction may play an important role in determining hazard potential associated with inhalation exposure to uranium materials. The fact that a larger rapidly dissolving fraction was observed in the airborne material than in the settled material indicates that dissolution analysis should be performed on appropriate size fraction samples. 20 references, 3 figures, 4 tables

Estimation of uranium in bioassay samples of occupational workers by laser fluorimetry

International Nuclear Information System (INIS)

Suja, A.; Prabhu, S.P.; Sawant, P.D.; Sarkar, P.K.; Tiwari, A.K.; Sharma, R.

2012-01-01

A newly established uranium processing facility has been commissioned at BARC, Trombay. Monitoring of occupational workers is essential to assess intake of uranium in this facility. A group of 21 workers was selected for bioassay monitoring to assess the existing urinary excretion levels of uranium before the commencement of actual work. Bioassay samples collected from these workers were analyzed by ion-exchange technique followed by laser fluorimetry. Standard addition method was followed for estimation of uranium concentration in the samples. The minimum detectable activity by this technique is about 0.2 ng. The range of uranium observed in these samples varies from 19 to 132 ng/L. Few of these samples were also analyzed by fission track analysis technique and the results were found to be comparable to those obtained by laser fluorimetry. The urinary excretion rate observed for the individual can be regarded as a 'personal baseline' and will be treated as the existing level of uranium in urine for these workers at the facility. (author)

Trace microanalysis of uranium in Indian tea samples

International Nuclear Information System (INIS)

Bansal, V.; Prasad, Rajendra

1991-01-01

The microscopic detection of radiation damage in plastic detectors has been used for the microanalysis of uranium contents in tea samples, commercially available in the market. The uranium concentration has been found to vary from 0.007±0.0001 to 0.12±0.001 ppm in various tea leaves. (author). 6 refs., 1 tab

Initiation of depleted uranium oxide and spent fuel testing for the spent fuel sabotage aerosol ratio program

Energy Technology Data Exchange (ETDEWEB)

Molecke, M.A.; Gregson, M.W.; Sorenson, K.B. [Sandia National Labs. (United States); Billone, M.C.; Tsai, H. [Argonne National Lab. (United States); Koch, W.; Nolte, O. [Fraunhofer Inst. fuer Toxikologie und Experimentelle Medizin (Germany); Pretzsch, G.; Lange, F. [Gesellschaft fuer Anlagen- und Reaktorsicherheit (Germany); Autrusson, B.; Loiseau, O. [Inst. de Radioprotection et de Surete Nucleaire (France); Thompson, N.S.; Hibbs, R.S. [U.S. Dept. of Energy (United States); Young, F.I.; Mo, T. [U.S. Nuclear Regulatory Commission (United States)

2004-07-01

We provide a detailed overview of an ongoing, multinational test program that is developing aerosol data for some spent fuel sabotage scenarios on spent fuel transport and storage casks. Experiments are being performed to quantify the aerosolized materials plus volatilized fission products generated from actual spent fuel and surrogate material test rods, due to impact by a high energy density device, HEDD. The program participants in the U.S. plus Germany, France, and the U.K., part of the international Working Group for Sabotage Concerns of Transport and Storage Casks, WGSTSC have strongly supported and coordinated this research program. Sandia National Laboratories, SNL, has the lead role for conducting this research program; test program support is provided by both the U.S. Department of Energy and Nuclear Regulatory Commission. WGSTSC partners need this research to better understand potential radiological impacts from sabotage of nuclear material shipments and storage casks, and to support subsequent risk assessments, modeling, and preventative measures. We provide a summary of the overall, multi-phase test design and a description of all explosive containment and aerosol collection test components used. We focus on the recently initiated tests on ''surrogate'' spent fuel, unirradiated depleted uranium oxide, and forthcoming actual spent fuel tests. The depleted uranium oxide test rodlets were prepared by the Institut de Radioprotection et de Surete Nucleaire, in France. These surrogate test rodlets closely match the diameter of the test rodlets of actual spent fuel from the H.B. Robinson reactor (high burnup PWR fuel) and the Surry reactor (lower, medium burnup PWR fuel), generated from U.S. reactors. The characterization of the spent fuels and fabrication into short, pressurized rodlets has been performed by Argonne National Laboratory, for testing at SNL. The ratio of the aerosol and respirable particles released from HEDD-impacted spent

Effects of depleted uranium on the reproductive success and F1 generation survival of zebrafish (Danio rerio)

Energy Technology Data Exchange (ETDEWEB)

Bourrachot, Stéphanie [Institut de Radioprotection et de Sûreté Nucléaire (IRSN), PRP-ENV/SERIS/LECO, Cadarache, Saint-Paul-lez-Durance 13115 (France); Brion, François [Institut National de l’Environnement Industriel et des Risques (INERIS), Unité d’évaluation des risques écotoxicologiques, BP2, 60550 Verneuil-en-Halatte (France); Pereira, Sandrine; Floriani, Magali; Camilleri, Virginie; Cavalié, Isabelle [Institut de Radioprotection et de Sûreté Nucléaire (IRSN), PRP-ENV/SERIS/LECO, Cadarache, Saint-Paul-lez-Durance 13115 (France); Palluel, Olivier [Institut National de l’Environnement Industriel et des Risques (INERIS), Unité d’évaluation des risques écotoxicologiques, BP2, 60550 Verneuil-en-Halatte (France); Adam-Guillermin, Christelle, E-mail: christelle.adam-guillermin@irsn.fr [Institut de Radioprotection et de Sûreté Nucléaire (IRSN), PRP-ENV/SERIS/LECO, Cadarache, Saint-Paul-lez-Durance 13115 (France)

2014-09-15

Highlights: • The effect of depleted uranium on zebrafish reproduction was studied. • An inhibition of egg production and an increase of F1 embryo mortality were observed. • Decreased circulating concentration of vitellogenin was observed in females. • Increased DNA damages were observed in parent gonads and in embryos. • U environmental concentration impairs reproduction and genetic integrity of fish. - Abstract: Despite the well-characterized occurrence of uranium (U) in the aquatic environment, very little is known about the chronic exposure of fish to low levels of U and its potential effect on reproduction. Therefore, this study was undertaken to investigate the effects of environmental concentrations of depleted U on the reproductive output of zebrafish (Danio rerio) and on survival and development of the F1 embryo-larvae following parental exposure to U. For that purpose, sexually mature male and female zebrafish were exposed to 20 and 250 μg/L of U for 14 days and allowed to reproduce in clean water during a further 14-day period. At all sampling times, whole-body vitellogenin concentrations and gonad histology were analyzed to investigate the effects of U exposure on these reproductive endpoints. In addition, accumulation of U in the gonads and its genotoxic effect on male and female gonad cells were quantified. The results showed that U strongly affected the capability of fish to reproduce and to generate viable individuals as evidenced by the inhibition of egg production and the increased rate of mortality of the F1 embryos. Interestingly, U exposure resulted in decreased circulating concentrations of vitellogenin in females. Increased concentrations of U were observed in gonads and eggs, which were most likely responsible for the genotoxic effects seen in fish gonads and in embryos exposed maternally to U. Altogether, these findings highlight the negative effect of environmentally relevant concentrations of U which alter the reproductive

Effects of depleted uranium on the reproductive success and F1 generation survival of zebrafish (Danio rerio)

International Nuclear Information System (INIS)

Bourrachot, Stéphanie; Brion, François; Pereira, Sandrine; Floriani, Magali; Camilleri, Virginie; Cavalié, Isabelle; Palluel, Olivier; Adam-Guillermin, Christelle

2014-01-01

Highlights: • The effect of depleted uranium on zebrafish reproduction was studied. • An inhibition of egg production and an increase of F1 embryo mortality were observed. • Decreased circulating concentration of vitellogenin was observed in females. • Increased DNA damages were observed in parent gonads and in embryos. • U environmental concentration impairs reproduction and genetic integrity of fish. - Abstract: Despite the well-characterized occurrence of uranium (U) in the aquatic environment, very little is known about the chronic exposure of fish to low levels of U and its potential effect on reproduction. Therefore, this study was undertaken to investigate the effects of environmental concentrations of depleted U on the reproductive output of zebrafish (Danio rerio) and on survival and development of the F1 embryo-larvae following parental exposure to U. For that purpose, sexually mature male and female zebrafish were exposed to 20 and 250 μg/L of U for 14 days and allowed to reproduce in clean water during a further 14-day period. At all sampling times, whole-body vitellogenin concentrations and gonad histology were analyzed to investigate the effects of U exposure on these reproductive endpoints. In addition, accumulation of U in the gonads and its genotoxic effect on male and female gonad cells were quantified. The results showed that U strongly affected the capability of fish to reproduce and to generate viable individuals as evidenced by the inhibition of egg production and the increased rate of mortality of the F1 embryos. Interestingly, U exposure resulted in decreased circulating concentrations of vitellogenin in females. Increased concentrations of U were observed in gonads and eggs, which were most likely responsible for the genotoxic effects seen in fish gonads and in embryos exposed maternally to U. Altogether, these findings highlight the negative effect of environmentally relevant concentrations of U which alter the reproductive

Depleted and enriched uranium exposure quantified in former factory workers and local residents of NL Industries, Colonie, NY USA

Energy Technology Data Exchange (ETDEWEB)

Arnason, John G. [Laboratory of Inorganic and Nuclear Chemistry, Wadsworth Center, New York State Department of Health, P.O. Box 509, Albany, NY 12201-0509 (United States); Department of Environmental Health Sciences, School of Public Health, The University at Albany, P.O. Box 509, Albany, NY 12201-0509 (United States); Pellegri, Christine N. [Laboratory of Inorganic and Nuclear Chemistry, Wadsworth Center, New York State Department of Health, P.O. Box 509, Albany, NY 12201-0509 (United States); Moore, June L.; Lewis-Michl, Elizabeth L. [Bureau of Environmental and Occupational Epidemiology, Center for Environmental Health, New York State Department of Health, Albany, NY (United States); Parsons, Patrick J., E-mail: patrick.parsons@health.ny.gov [Laboratory of Inorganic and Nuclear Chemistry, Wadsworth Center, New York State Department of Health, P.O. Box 509, Albany, NY 12201-0509 (United States); Department of Environmental Health Sciences, School of Public Health, The University at Albany, P.O. Box 509, Albany, NY 12201-0509 (United States)

2016-10-15

Background: Between 1958 and 1982, NL Industries manufactured components of enriched (EU) and depleted uranium (DU) at a factory in Colonie NY, USA. More than 5 metric tons of DU was deposited as microscopic DU oxide particles on the plant site and surrounding residential community. A prior study involving a small number of individuals (n=23) indicated some residents were exposed to DU and former workers to both DU and EU, most probably through inhalation of aerosol particles. Objectives: Our aim was to measure total uranium [U] and the uranium isotope ratios: {sup 234}U/{sup 238}U; {sup 235}U/{sup 238}U; and {sup 236}U/{sup 238}U, in the urine of a cohort of former workers and nearby residents of the NLI factory, to characterize individual exposure to natural uranium (NU), DU, and EU more than 3 decades after production ceased. Methods: We conducted a biomonitoring study in a larger cohort of 32 former workers and 99 residents, who may have been exposed during its period of operation, by measuring Total U, NU, DU, and EU in urine using Sector Field Inductively Coupled Plasma - Mass Spectrometry (SF-ICP-MS). Results: Among workers, 84% were exposed to DU, 9% to EU and DU, and 6% to natural uranium (NU) only. For those exposed to DU, urinary isotopic and [U] compositions result from binary mixing of NU and the DU plant feedstock. Among residents, 8% show evidence of DU exposure, whereas none shows evidence of EU exposure. For residents, the [U] geometric mean is significantly below the value reported for NHANES. There is no significant difference in [U] between exposed and unexposed residents, suggesting that [U] alone is not a reliable indicator of exposure to DU in this group. Conclusions: Ninety four percent of workers tested showed evidence of exposure to DU, EU or both, and were still excreting DU and EU decades after leaving the workforce. The study demonstrates the advantage of measuring multiple isotopic ratios (e.g., {sup 236}U/{sup 238}U and {sup 235}U

Investigations in hydrogeochemical samples for uranium exploration

International Nuclear Information System (INIS)

Krishnakumar, M.

2015-01-01

The primary mandate of Atomic Minerals Directorate for Exploration and Research (AMD) is to explore and establish the uranium and other atomic mineral resources required for the country's nuclear power programme. During the geochemical exploration, a large number of ground, surface, spring, stream and lake water samples are collected and analysed for various parameters. These include physical parameters such as temperature, pH, Eh, electrical conductivity etc., and concentrations of uranium and multi-ions at mg/L to ng/L using state-of-the-art instrumental analytical techniques. Hydrogeochemical analysis is considered to be a cost effective and rapid exploration tool for getting sub-surface information leading to finding of concealed uranium deposits. Water samples from a bore well, dug well, stream, spring which is in dynamic equilibrium with the rocks are collected in a white, thick walled, non-transparent, non-recycled and air-tight container, stored and analysed within eight hours if possible to avoid change in Eh-pH conditions and precipitation-dissolution of trace elements

Determination of uranium concentration in an ore sample using laser-induced breakdown spectroscopy

International Nuclear Information System (INIS)

Kim, Y.-S.; Han, B.-Y.; Shin, H.S.; Kim, H.D.; Jung, E.C.; Jung, J.H.; Na, S.H.

2012-01-01

Laser-induced breakdown spectroscopy (LIBS) has been recognized as a promising technique for analyzing sensitive nuclear materials such as uranium, plutonium, and curium in a high-radiation environment, especially since the implementation of IAEA (International Atomic Energy Agency) safeguards. The uranium spectra of ore samples were quantitatively analyzed prior to analyzing sensitive materials in the nuclear industry. The purpose of this experiment is to extract quantitative information about the uranium in a uranium ore using a standard addition approach. The uranium ore samples containing different concentrations of U were prepared by mixing raw ore powder with natural uranium oxide powders. Calibration sets of 0.2, 0.4, 0.6, 0.8 and 1.0 wt.% uranium concentrations within the uranium ore sample were achieved. A pulsed and Q-switched Nd:YAG laser at a wavelength of 532 nm was used as a light source. An echelle spectrometer that covers a 190–420 nm wavelength range is used to generate a calibration curve and determine the detection limit of uranium in the ore matrix. The neutral atomic-emission peak at a wavelength of 356.659 nm indicated a detection limit of ∼ 158 ppm for uranium, and the uranium concentration was determined in a raw ore sample that has an unknown quantity of uranium. - Highlights: ► The feasibility of LIBS application to monitor uranium element was carried out. ► The detection limit of U in ore was determined by a standard additional approach. ► Quantitative analyses of U concentration in a natural uranium ore were performed.

Effects of depleted uranium on the health and survival of Ceriodaphnia dubia and Hyalella azteca

Science.gov (United States)

Kuhne, W.W.; Caldwell, C.A.; Gould, W.R.; Fresquez, P.R.; Finger, S.

2002-01-01

Depleted uranium (DU) has been used as a substitute for the fissionable enriched uranium component of atomic weapons tested at Los Alamos National Laboratory (LANL) (Los Alamos, NM, USA) since the early 1950s, resulting in considerable concentrations of DU in the soils within the test sites. Although the movement of DU into major aquatic systems has been shown to be minimal, there are many small-order ephemeral streams and areas of standing water in canyons throughout LANL that may be affected by inputs of DU via runoff, erosion, and leaching. Ninety-six-hour acute and 7-d chronic toxicity assays were conducted to measure the toxicity of DU on survival and reproduction of Ceriodaphnia dubia. A 14-d water-only assay was conducted to measure survival and growth of Hyalella azteca. The estimated median lethal concentration (LC50) to produce 50% mortality of the test population for the 96-h Ceriodaphnia dubia assay was 10.50 mg/L. Reproductive effects occurred at a lowest-observable-effect concentration ???3.91 mg/L with a no-observable-effect concentration of 1.97 mg/L. The estimated 14-d LC50 for the Hyalella azteca assay was 1.52 mg/L No significant relationship was detected between growth and DU concentrations. Concentrations at which toxicity effects were observed in this study for both invertebrates exceeded concentrations of total uranium observed in runoff from LANL lands. Thus, it is likely that current runoff levels of uranium do not pose a threat to these types of aquatic invertebrates.

Solid state speciation and potential bioavailability of depleted uranium particles from Kosovo and Kuwait

Energy Technology Data Exchange (ETDEWEB)

Lind, O.C. [Isotope Laboratory, Department of Plant and Environmental Sciences, Norwegian University of Life Sciences, P.O. Box 5003, N-1432 As (Norway)], E-mail: ole-christian.lind@umb.no; Salbu, B.; Skipperud, L. [Isotope Laboratory, Department of Plant and Environmental Sciences, Norwegian University of Life Sciences, P.O. Box 5003, N-1432 As (Norway); Janssens, K.; Jaroszewicz, J.; De Nolf, W. [Department of Chemistry, University of Antwerp, Universiteitsplein 1, Antwerp (Belgium)

2009-04-15

A combination of synchrotron radiation based X-ray microscopic techniques ({mu}-XRF, {mu}-XANES, {mu}-XRD) applied on single depleted uranium (DU) particles and semi-bulk leaching experiments has been employed to link the potential bioavailability of DU particles to site-specific particle characteristics. The oxidation states and crystallographic forms of U in DU particles have been determined for individual particles isolated from selected samples collected at different sites in Kosovo and Kuwait that were contaminated by DU ammunition during the 1999 Balkan conflict and the 1991 Gulf war. Furthermore, small soil or sand samples heavily contaminated with DU particles were subjected to simulated gastrointestinal fluid (0.16 M HCl) extractions. Characteristics of DU particles in Kosovo soils collected in 2000 and in Kuwait soils collected in 2002 varied significantly depending on the release scenario and to some extent on weathering conditions. Oxidized U (+6) was determined in large, fragile and bright yellow DU particles released during fire at a DU ammunition storage facility and crystalline phases such as schoepite (UO{sub 3}.2.25H{sub 2}O), dehydrated schoepite (UO{sub 3}.0.75H{sub 2}O) and metaschoepite (UO{sub 3}.2.0H{sub 2}O) were identified. As expected, these DU particles were rapidly dissolved in 0.16 M HCl (84 {+-} 3% extracted after 2 h) indicating a high degree of potential mobility and bioavailability. In contrast, the 2 h extraction of samples contaminated with DU particles originating either from corrosion of unspent DU penetrators or from impacted DU ammunition appeared to be much slower (20-30%) as uranium was less oxidized (+4 to +6). Crystalline phases such as UO{sub 2}, UC and metallic U or U-Ti alloy were determined in impacted DU particles from Kosovo and Kuwait, while the UO{sub 2,34} phase, only determined in particles from Kosovo, could reflect a more corrosive environment. Although the results are based on a limited number of DU particles

Rapid extraction and assay of uranium from environmental surface samples

Energy Technology Data Exchange (ETDEWEB)

Barrett, Christopher A.; Chouyyok, Wilaiwan; Speakman, Robert J.; Olsen, Khris B.; Addleman, Raymond Shane

2017-10-01

Extraction methods enabling faster removal and concentration of uranium compounds for improved trace and low-level assay are demonstrated for standard surface sampling material in support of nuclear safeguards efforts, health monitoring, and other nuclear analysis applications. A key problem with the existing surface sampling swipes is the requirement for complete digestion of sample and sampling matrix. This is a time-consuming and labour-intensive process that limits laboratory throughput, elevates costs, and increases background levels. Various extraction methods are explored for their potential to quickly and efficiently remove different chemical forms of uranium from standard surface sampling material. A combination of carbonate and peroxide solutions is shown to give the most rapid and complete form of uranyl compound extraction and dissolution. This rapid extraction process is demonstrated to be compatible with standard inductive coupled plasma mass spectrometry methods for uranium isotopic assay as well as screening techniques such as x-ray fluorescence. The general approach described has application beyond uranium to other analytes of nuclear forensic interest (e.g., rare earth elements and plutonium) as well as heavy metals for environmental and industrial hygiene monitoring.

Depleted uranium induces neoplastic transformation in human lung epithelial cells.

Science.gov (United States)

Xie, Hong; LaCerte, Carolyne; Thompson, W Douglas; Wise, John Pierce

2010-02-15

Depleted uranium (DU) is commonly used in military armor and munitions, and thus, exposure of soldiers and noncombatants is frequent and widespread. Previous studies have shown that DU has both chemical and radiological toxicity and that the primary route of exposure of DU to humans is through inhalation and ingestion. However, there is limited research information on the potential carcinogenicity of DU in human bronchial cells. Accordingly, we determined the neoplastic transforming ability of particulate DU to human bronchial epithelial cells (BEP2D). We observed the loss of contact inhibition and anchorage independent growth in cells exposed to DU after 24 h. We also characterized these DU-induced transformed cell lines and found that 40% of the cell lines exhibit alterations in plating efficiency and no significant changes in the cytotoxic response to DU. Cytogenetic analyses showed that 53% of the DU-transformed cell lines possess a hypodiploid phenotype. These data indicate that human bronchial cells are transformed by DU and exhibit significant chromosome instability consistent with a neoplastic phenotype.

Characterisation and dissolution of depleted uranium aerosols produced during impacts of kinetic energy penetrators against a tank

Energy Technology Data Exchange (ETDEWEB)

Chazel, V.; Gerasimo, P.; Debouis, V.; Laroche, P.; Paquet, F

2003-07-01

Aerosols produced during impacts of depleted uranium (DU) penetrators against the glacis (sloping armour) and the turret of a tank were sampled. The concentration and size distribution were determined. Activity median aerodynamic diameters were 1 {mu}m (geometric standard deviation, s{sub g} = 3.7) and 2 {mu}m (s{sub g} = 2.5), respectively, for glacis and turret. The mean air concentration was 120 Bq m{sup -3}, i.e. 8.5 mg m{sup -3} of DU. Filters analysed by scanning electron microscopy (SEM) and X ray diffraction showed two types of particles (fine particles and large molten particles) composed mainly of a mixture of uranium and aluminium. The uranium oxides were mostly U{sub 3}O{sub 8}, UO{sub 2.25} and probably UO{sub 3.01} and a mixed compound of U and Al. The kinetics of dissolution in three media (HCO{sub 3}{sup -}, HCl and Gamble's solution) were determined using in-vitro tests. The slow dissolution rates were respectively slow, and intermediate between slow and moderate, and the rapid dissolution fractions were mostly intermediate between moderate and fast. According to the in-vitro results for Gamble's solution, and based on a hypothetical single acute inhalation of 90 Bq, effective doses integrated up to 1 y after incorporation were 0.54 and 0.56 mSv respectively, for aerosols from glacis and turret. In comparison, the ICRP limits are 20 mSv y{sup -1} for workers and 1 mSv y{sup -1} for members of public. A kidney concentration of approximately 0.1 {mu}g U g{sup -1} was predicted and should not, in this case, lead to kidney damage. (author)

Uranium isotopic signatures measured in samples of dirt collected at two former uranium facilities

International Nuclear Information System (INIS)

Meyers, L.A.; Stalcup, A.M.; LaMont, S.P.; Spitz, H.B.

2014-01-01

Nuclear forensics is a multidisciplinary science that uses a variety of analytical methods and tools to explore the physical, chemical, and isotopic characteristics of nuclear and radiological materials. These characteristics, when evaluated alone or in combination, become signatures that may reveal how and when the material was fabricated. The signatures contained in samples of dirt collected at two different uranium metal processing facilities in the United States were evaluated to determine uranium isotopic composition and compare results with processes that were conducted at these sites. One site refined uranium and fabricated uranium metal ingots for fuel and targets and the other site rolled hot forged uranium and other metals into dimensional rods. Unique signatures were found that are consistent with the activities and processes conducted at each facility and establish confidence in using these characteristics to reveal the provenance of other materials that exhibit similar signatures. (author)

Depleted uranium induces sex- and tissue-specific methylation patterns in adult zebrafish

International Nuclear Information System (INIS)

Gombeau, Kewin; Pereira, Sandrine; Ravanat, Jean-Luc; Camilleri, Virginie; Cavalie, Isabelle; Bourdineaud, Jean-Paul; Adam-Guillermin, Christelle

2016-01-01

We examined the effects of chronic exposure to different concentrations (2 and 20 μg L"−"1) of environmentally relevant waterborne depleted uranium (DU) on the DNA methylation patterns both at HpaII restriction sites (5′-CCGG-3′) and across the whole genome in the zebrafish brain, gonads, and eyes. We first identified sex-dependent differences in the methylation level of HpaII sites after exposure. In males, these effects were present as early as 7 days after exposure to 20 μg L"−"1 DU, and were even more pronounced in the brain, gonads, and eyes after 24 days. However, in females, hypomethylation was only observed in the gonads after exposure to 20 μg L"−"1 DU for 24 days. Sex-specific effects of DU were also apparent at the whole-genome level, because in males, exposure to 20 μg L"−"1 DU for 24 days resulted in cytosine hypermethylation in the brain and eyes and hypomethylation in the gonads. In contrast, in females, hypermethylation was observed in the brain after exposure to both concentrations of DU for 7 days. Based on our current knowledge of uranium toxicity, several hypotheses are proposed to explain these findings, including the involvement of oxidative stress, alteration of demethylation enzymes and the calcium signaling pathway. This study reports, for the first time, the sex- and tissue-specific epigenetic changes that occur in a nonhuman organism after exposure to environmentally relevant concentrations of uranium, which could induce transgenerational epigenetic effects. - Highlights: • This study demonstrates a sex-related effect of DU exposure on DNA methylation patterns. • Impacts on DNA methylation patterns revealed a tissue-specific effect of DU exposure. • The MS–AFLP and HPLC–MS/MS sensitively and complementarily demonstrated the responses to environmental concentrations of DU.

Haematological malignancies in childhood in Croatia: Investigating the theories of depleted uranium, chemical plant damage and 'population mixing'

International Nuclear Information System (INIS)

Labar, B.; Rudan, I.; Ivankovic, D.; Biloglav, Z.; Mrsic, M.; Strnad, M.; Fucic, A.; Znaor, A.; Bradic, T.; Campbell, H.

2004-01-01

Some of potential causes proposed to explain the reported increase of haematological malignancies in childhood during or after the war period in several countries include depleted uranium, chemical pollution and population mixing theory. The aim of this study was to define the population of Croatian children aged 0-14 years who were potentially exposed to each of those risks during the war and to investigate any possible association between the exposure and the incidence of haematological malignancies. The authors analyzed the data reported by the Cancer Registry of Croatia during the pre-war period (1986-1990), war period (1991-1995) and post-war period (1996-1999). In the group of 10 counties potentially exposed to depleted uranium and two counties where chemical war damage occurred, no significant difference in incidence of the studied haematological malignancies was noted in comparison to pre-war period. The incidence of lymphatic leukaemia significantly increased in four counties where population mixing had occurred during the war period, supporting the 'mixing theory'. In those counties, the incidence of Hodgkin's lymphoma decreased during and after the war. In Croatia as a whole, decreases in incidence of myeloid leukaemias during war and non-Hodgkin lymphoma after the war were noted

Electrically Heated Testing of the Kilowatt Reactor Using Stirling Technology (KRUSTY) Experiment Using a Depleted Uranium Core

Science.gov (United States)

Briggs, Maxwell H.; Gibson, Marc A.; Sanzi, James

2017-01-01

The Kilopower project aims to develop and demonstrate scalable fission-based power technology for systems capable of delivering 110 kW of electric power with a specific power ranging from 2.5 - 6.5 Wkg. This technology could enable high power science missions or could be used to provide surface power for manned missions to the Moon or Mars. NASA has partnered with the Department of Energys National Nuclear Security Administration, Los Alamos National Labs, and Y-12 National Security Complex to develop and test a prototypic reactor and power system using existing facilities and infrastructure. This technology demonstration, referred to as the Kilowatt Reactor Using Stirling TechnologY (KRUSTY), will undergo nuclear ground testing in the summer of 2017 at the Nevada Test Site. The 1 kWe variation of the Kilopower system was chosen for the KRUSTY demonstration. The concept for the 1 kWe flight system consist of a 4 kWt highly enriched Uranium-Molybdenum reactor operating at 800 degrees Celsius coupled to sodium heat pipes. The heat pipes deliver heat to the hot ends of eight 125 W Stirling convertors producing a net electrical output of 1 kW. Waste heat is rejected using titanium-water heat pipes coupled to carbon composite radiator panels. The KRUSTY test, based on this design, uses a prototypic highly enriched uranium-molybdenum core coupled to prototypic sodium heat pipes. The heat pipes transfer heat to two Advanced Stirling Convertors (ASC-E2s) and six thermal simulators, which simulate the thermal draw of full scale power conversion units. Thermal simulators and Stirling engines are gas cooled. The most recent project milestone was the completion of non-nuclear system level testing using an electrically heated depleted uranium (non-fissioning) reactor core simulator. System level testing at the Glenn Research Center (GRC) has validated performance predictions and has demonstrated system level operation and control in a test configuration that replicates the one

Uranium and thorium determination in water samples taken along River Kura

International Nuclear Information System (INIS)

Ahmadov, M.M.; Ibadov, N.A.; Safarova, K.S.; Humbatov, F.Y.; Suleymanov, B.A.

2014-01-01

Full text : In the present investigation, uranium and thorium concentration in rivers water of Azerbaijan has been measured using inductively coupled plasma mass spectrometry. The Agilent 7700x series ICP-MS applied for analysis of water samples. This method is based on direct introduction of samples, without any chemical pre-treatment, into an inductively coupled plasma plasma mass spectrometer. Uranium and thorium was determined at the mass mass numbers of 238 and 232 respectively using Bi-209 as internal standard. The main purpose of the study is to measure the level of uranium and thorium in water samples taken along river Kura

Rapid uranium analysis by delayed neutron counting of neutron activated samples

International Nuclear Information System (INIS)

Papadopoulos, N.N.

1985-01-01

The uranium analyzer at the Nuclear Research Center ''Demokritos'' and the delayed neutron method have been used to determine the uranium content in lignite, in chemically enriched samples and in solutions of extractable uranium. The results are compared with data obtained by other methods. In the case of dissolved extractable uranium. The results are in good agreement with X-ray fluorescence data in the range 100 ppm to 2000 ppm while beyond these limits the discrepancies between neutron and spectrophotometric data are observed. The results for lignite samples are in good agreement with gamma spectrometric data. Discrepancies indicate that more extensive intercomparisons are needed to check the reliability of various methods

Implication of neuro-genesis during brain development in behavior disorders caused by depleted uranium

International Nuclear Information System (INIS)

Legrand, Marie

2016-01-01

Humans are continuously exposed to neurotoxic compounds in the environment. The developing brain is more susceptible to neurotoxic compounds and modifications in its growth could lead to disorders in adulthood. Uranium (U) is an environmental heavy metal and induces behavioral disorders as well as affects neurochemistry. The aim of my thesis was to investigate whether depleted uranium (DU) exposure affects neuro-genesis processes, which are implicated in brain development and in synaptic plasticity in adults. While DU increased cell proliferation in the hippocampal neuro-epithelium and decreased cell death at prenatal stages, DU lead to opposite effects in the dentate gyrus at postnatal stages. Moreover, DU had an inhibitory effect on the transition toward neuronal differentiation pathway during development. At adult stage, DU induced a decrease in neuronal differentiation but has no impact in cell proliferation. Finally, DU exposure during brain development caused depressive like behavior at late postnatal and adult stage, and decreased spatial memory at adult stage. Consequently, DU exposure during brain development caused modification in neuro-genesis processes associated to cognitive and emotional disorders at adult age. U could present a threat to human health, especially in pregnant women and children. (author)

Trace determination of uranium in fertilizer samples by total ...

Indian Academy of Sciences (India)

the fertilizers is important because it can be used as fuel in nuclear reactors and also because of en- vironmental concerns. ... The amounts of uranium in four fertilizer samples of Hungarian origin were determined by ... TXRF determination of uranium from phosphate fertilizers of Hungarian origin and the preliminary results ...

Simultaneous determination of plutonium and uranium in environmental samples

International Nuclear Information System (INIS)

Jiao Shufen

1993-01-01

Plutonium and uranium in a plant sample ash was simultaneously determined by using anion exchange resin columns, and concentrated hydrochloric acid and nitric acid. At the final stage of the determination of the nuclides, each of them was electrodeposited together with a little amount of molybdenum carrier onto a stainless steel plate and measured by α-ray spectrometer. The recoveries of uranium and plutonium from the plant samples determined by adding internal standard 236 Pu which was 100% and 63%, respectively

The health hazards of depleted uranium munitions. Part 1

Energy Technology Data Exchange (ETDEWEB)

NONE

2001-05-01

There has been a substantial amount of public discussion on the health effects of the use of depleted uranium (DU), especially on the battlefield. The RoyaI Society therefore convened an independent expert Working Group to review the present state of scientific knowledge about the health and environmental effects of DU, in order to inform public debate. This is the first of two reports. It deals with the amounts of DU to which soldiers could be exposed on the battlefield, the risks from radiation, and what we know from epidemiological studies. We consider past and potential future exposures, the most likely exposures and the 'worst-case' exposures that cannot be excluded. Our second report, to be published later this year, will address the risks from toxic poisoning and environmental issues including risks to civilian populations. The group has consulted widely. It has focused on what is known scientifically about aspects that are relevant to health and has not considered the merits of using DU in munitions. Nor does this report analyse Gulf War syndrome, which has been the subject of other reports. DU is a toxic and weakly radioactive heavy metal that may have adverse consequences to human health, particularly if it enters the body through inhalation, ingestion or wounding. On the battlefield it is used in kinetic energy weapons designed to penetrate the armour of tanks and other vehicles. On impact substantial amounts of DU may be dispersed as particles that can be inhaled and as shrapnel. Our approach has been to estimate the typical levels of exposure on the battlefield over a wide range of scenarios, and the worst-case exposures that individuals are unlikely to exceed. From these we calculate the potential health risks from radiation. We have also considered epidemiological studies of occupational exposures to uranium in other situations as an independent source of information on the risks of inhaling DU particles, although we recognise that the

The health hazards of depleted uranium munitions. Part 1

International Nuclear Information System (INIS)

2001-01-01

There has been a substantial amount of public discussion on the health effects of the use of depleted uranium (DU), especially on the battlefield. The RoyaI Society therefore convened an independent expert Working Group to review the present state of scientific knowledge about the health and environmental effects of DU, in order to inform public debate. This is the first of two reports. It deals with the amounts of DU to which soldiers could be exposed on the battlefield, the risks from radiation, and what we know from epidemiological studies. We consider past and potential future exposures, the most likely exposures and the 'worst-case' exposures that cannot be excluded. Our second report, to be published later this year, will address the risks from toxic poisoning and environmental issues including risks to civilian populations. The group has consulted widely. It has focused on what is known scientifically about aspects that are relevant to health and has not considered the merits of using DU in munitions. Nor does this report analyse Gulf War syndrome, which has been the subject of other reports. DU is a toxic and weakly radioactive heavy metal that may have adverse consequences to human health, particularly if it enters the body through inhalation, ingestion or wounding. On the battlefield it is used in kinetic energy weapons designed to penetrate the armour of tanks and other vehicles. On impact substantial amounts of DU may be dispersed as particles that can be inhaled and as shrapnel. Our approach has been to estimate the typical levels of exposure on the battlefield over a wide range of scenarios, and the worst-case exposures that individuals are unlikely to exceed. From these we calculate the potential health risks from radiation. We have also considered epidemiological studies of occupational exposures to uranium in other situations as an independent source of information on the risks of inhaling DU particles, although we recognise that the parallels may

Uranium quantification in semen by inductively coupled plasma mass spectrometry

Science.gov (United States)

Todorov, Todor I.; Ejnik, John W.; Guandalini, Gustavo S.; Xu, Hanna; Hoover, Dennis; Anderson, Larry W.; Squibb, Katherine; McDiarmid, Melissa A.; Centeno, Jose A.

2013-01-01

In this study we report uranium analysis for human semen samples. Uranium quantification was performed by inductively coupled plasma mass spectrometry. No additives, such as chymotrypsin or bovine serum albumin, were used for semen liquefaction, as they showed significant uranium content. For method validation we spiked 2 g aliquots of pooled control semen at three different levels of uranium: low at 5 pg/g, medium at 50 pg/g, and high at 1000 pg/g. The detection limit was determined to be 0.8 pg/g uranium in human semen. The data reproduced within 1.4–7% RSD and spike recoveries were 97–100%. The uranium level of the unspiked, pooled control semen was 2.9 pg/g of semen (n = 10). In addition six semen samples from a cohort of Veterans exposed to depleted uranium (DU) in the 1991 Gulf War were analyzed with no knowledge of their exposure history. Uranium levels in the Veterans’ semen samples ranged from undetectable (<0.8 pg/g) to 3350 pg/g. This wide concentration range for uranium in semen is consistent with known differences in current DU body burdens in these individuals, some of whom have retained embedded DU fragments.

Mobility of elevated levels of uranium in the environment

International Nuclear Information System (INIS)

Miera, F.R. Jr.; Hanson, W.C.; Gladney, E.S.; Jose, P.

1980-01-01

Studies of the long-term consequences of exposing terrestrial ecosystems to aged deposits of natural and depleted uranium at Los Alamos Scientific Laboratory (LASL) have been conducted over the past 3 years. The E-F explosive testing site at LASL was selected for intensive study of uranium redistribution during its 24-year use. The highest surface-soil (0 to 2.5 cm) uranium concentrations occurred 0 to 10 m from the detonation point and average 4500 μg/g. Concentrations in surface soil 50 and 200 m from the detonation point were generally less than 15% of that value. The uranium distribution to 30-cm depths for the 0- to 50-m distant sampling locations and to 10-cm depths at 50- to 200-m sampling distances showed significant penetration into the soil profile. Ratios of plant/soil uranium concentrations varied from 0.05 to 0.08. Internal tissues from two species of small mammals had tissue/soil ratios of 10 -3 and 10 -4

Experimental evaluation of the detection threshold of uranium in urine samples

International Nuclear Information System (INIS)

Ferreyra, M. D.; Suarez Mendez, Sebastian; Tossi, Mirta H.

1999-01-01

The routine internal dosimetric tests for nuclear installations workers includes the determination of uranium in urine. The analysis is carried out, after chemical treatment, by UV fluorometry, comparing the results with urine blank samples from workers not exposed professionally to contamination. The fluctuation of the results of the uranium content in the blank samples greatly affects the determinations. In 30 blank samples the uranium content was determined and the results were evaluated by three calculation methods: 1) The procedure recommended by IUPAC; 2) The graphical method; 3) and The error propagation method. The last one has been adopted for the calculation of the detection threshold. (authors)

Long-term fate of depleted uranium at Aberdeen and Yuma Proving Grounds: Human health and ecological risk assessments

Energy Technology Data Exchange (ETDEWEB)

Ebinger, M.H.; Beckman, R.J.; Myers, O.B. [Los Alamos National Lab., NM (United States); Kennedy, P.L.; Clements, W.; Bestgen, H.T. [Colorado State Univ., Ft. Collins, CO (United States). Dept. of Fishery and Wildlife Biology

1996-09-01

The purpose of this study was to evaluate the immediate and long-term consequences of depleted uranium (DU) in the environment at Aberdeen Proving Ground (APG) and Yuma Proving Ground (YPG) for the Test and Evaluation Command (TECOM) of the US Army. Specifically, we examined the potential for adverse radiological and toxicological effects to humans and ecosystems caused by exposure to DU at both installations. We developed contaminant transport models of aquatic and terrestrial ecosystems at APG and terrestrial ecosystems at YPG to assess potential adverse effects from DU exposure. Sensitivity and uncertainty analyses of the initial models showed the portions of the models that most influenced predicted DU concentrations, and the results of the sensitivity analyses were fundamental tools in designing field sampling campaigns at both installations. Results of uranium (U) isotope analyses of field samples provided data to evaluate the source of U in the environment and the toxicological and radiological doses to different ecosystem components and to humans. Probabilistic doses were estimated from the field data, and DU was identified in several components of the food chain at APG and YPG. Dose estimates from APG data indicated that U or DU uptake was insufficient to cause adverse toxicological or radiological effects. Dose estimates from YPG data indicated that U or DU uptake is insufficient to cause radiological effects in ecosystem components or in humans, but toxicological effects in small mammals (e.g., kangaroo rats and pocket mice) may occur from U or DU ingestion. The results of this study were used to modify environmental radiation monitoring plans at APG and YPG to ensure collection of adequate data for ongoing ecological and human health risk assessments.

Long-term fate of depleted uranium at Aberdeen and Yuma Proving Grounds: Human health and ecological risk assessments

International Nuclear Information System (INIS)

Ebinger, M.H.; Beckman, R.J.; Myers, O.B.; Kennedy, P.L.; Clements, W.; Bestgen, H.T.

1996-09-01

The purpose of this study was to evaluate the immediate and long-term consequences of depleted uranium (DU) in the environment at Aberdeen Proving Ground (APG) and Yuma Proving Ground (YPG) for the Test and Evaluation Command (TECOM) of the US Army. Specifically, we examined the potential for adverse radiological and toxicological effects to humans and ecosystems caused by exposure to DU at both installations. We developed contaminant transport models of aquatic and terrestrial ecosystems at APG and terrestrial ecosystems at YPG to assess potential adverse effects from DU exposure. Sensitivity and uncertainty analyses of the initial models showed the portions of the models that most influenced predicted DU concentrations, and the results of the sensitivity analyses were fundamental tools in designing field sampling campaigns at both installations. Results of uranium (U) isotope analyses of field samples provided data to evaluate the source of U in the environment and the toxicological and radiological doses to different ecosystem components and to humans. Probabilistic doses were estimated from the field data, and DU was identified in several components of the food chain at APG and YPG. Dose estimates from APG data indicated that U or DU uptake was insufficient to cause adverse toxicological or radiological effects. Dose estimates from YPG data indicated that U or DU uptake is insufficient to cause radiological effects in ecosystem components or in humans, but toxicological effects in small mammals (e.g., kangaroo rats and pocket mice) may occur from U or DU ingestion. The results of this study were used to modify environmental radiation monitoring plans at APG and YPG to ensure collection of adequate data for ongoing ecological and human health risk assessments

A study on the oxidation behavior of uranium

International Nuclear Information System (INIS)

Kim, Tae Kook; Kang, Kweon Ho; Kim, Kil Jeang; Kang, Il Sik; Jung, Kyung Whan

1998-03-01

When storing depleted uranium wastes, careful handling is required due to their very high oxidation rates. To determine the oxidation mechanism and oxidation rate of depleted uranium wastes, the most important factors to be considered in their treatment, an experiment was carried out by varying the heating rates of the Air-Controlled Oxidizer. The experiment, showed that depleted uranium wastes are pulverized after complete oxidation because of the density difference and then converted to UO 2 , U 3 O 7 , U 3 O 8 . The grain size of pulverized powder decrease with increased temperature. (author). 30 refs., 5 tabs., 28 figs

Characterization of Uranium Contamination, Transport, and Remediation at Rocky Flats - Across Remediation into Post-Closure

Science.gov (United States)

Janecky, D. R.; Boylan, J.; Murrell, M. T.

2009-12-01

The Rocky Flats Site is a former nuclear weapons production facility approximately 16 miles northwest of Denver, Colorado. Built in 1952 and operated by the Atomic Energy Commission and then Department of Energy, the Site was remediated and closed in 2005, and is currently undergoing long-term surveillance and monitoring by the DOE Office of Legacy Management. Areas of contamination resulted from roughly fifty years of operation. Of greatest interest, surface soils were contaminated with plutonium, americium, and uranium; groundwater was contaminated with chlorinated solvents, uranium, and nitrates; and surface waters, as recipients of runoff and shallow groundwater discharge, have been contaminated by transport from both regimes. A region of economic mineralization that has been referred to as the Colorado Mineral Belt is nearby, and the Schwartzwalder uranium mine is approximately five miles upgradient of the Site. Background uranium concentrations are therefore elevated in many areas. Weapons-related activities included work with enriched and depleted uranium, contributing anthropogenic content to the environment. Using high-resolution isotopic analyses, Site-related contamination can be distinguished from natural uranium in water samples. This has been instrumental in defining remedy components, and long-term monitoring and surveillance strategies. Rocky Flats hydrology interlinks surface waters and shallow groundwater (which is very limited in volume and vertical and horizontal extent). Surface water transport pathways include several streams, constructed ponds, and facility surfaces. Shallow groundwater has no demonstrated connection to deep aquifers, and includes natural preferential pathways resulting primarily from porosity in the Rocky Flats alluvium, weathered bedrock, and discontinuous sandstones. In addition, building footings, drains, trenches, and remedial systems provide pathways for transport at the site. Removal of impermeable surfaces (buildings

Lichens as biomonitors of uranium in the Balkan area

International Nuclear Information System (INIS)

Loppi, S.; Riccobono, F.; Zhang, Z.H.; Savic, S.; Ivanov, D.; Pirintsos, S.A.

2003-01-01

Widespread contamination by depleted uranium was not detected in the Balkan area. - The contribution of the conflict of 1999 to the environmental levels of uranium in the Balkan area was evaluated by means of lichens used as biomonitors. The average U concentration found in lichens in the present study was in line with the values reported for lichens from other countries and well below the levels found in lichens collected in areas with natural or anthropogenic sources of U. Measurement of isotopic ratios 235 U/ 238 U allowed to exclude the presence of depleted uranium. According to these results, we could not detect widespread environmental contamination by depleted uranium in the Balkan area

Lichens as biomonitors of uranium in the Balkan area

Energy Technology Data Exchange (ETDEWEB)

Loppi, S.; Riccobono, F.; Zhang, Z.H.; Savic, S.; Ivanov, D.; Pirintsos, S.A

2003-09-01

Widespread contamination by depleted uranium was not detected in the Balkan area. - The contribution of the conflict of 1999 to the environmental levels of uranium in the Balkan area was evaluated by means of lichens used as biomonitors. The average U concentration found in lichens in the present study was in line with the values reported for lichens from other countries and well below the levels found in lichens collected in areas with natural or anthropogenic sources of U. Measurement of isotopic ratios {sup 235}U/{sup 238}U allowed to exclude the presence of depleted uranium. According to these results, we could not detect widespread environmental contamination by depleted uranium in the Balkan area.

Preconcentration of uranium in water samples using dispersive ...

African Journals Online (AJOL)

Preconcentration of uranium in water samples using dispersive liquid-liquid micro- extraction coupled with solid-phase extraction and determination with inductively coupled plasma-optical emission spectrometry.

Decreases in soil microbial function and functional diversity in response to depleted uranium

International Nuclear Information System (INIS)

Meyer, M.C.; Paschke, M.W.; McLendon, T.

1998-01-01

A soil microcosm experiment was used to analyze effects of depleted uranium (DU) on soil function, and the concomitant changes in bacterial functional diversity. Uranium treatment levels were 0, 50, 500, 5000, 10,000 and 25,000 mg DU kg -1 soil. Three measures of soil function were made. Overall soil biological activity was assessed via measurement of soil respiration. Decomposition was assessed by measurement of mass loss of four different plant litter types: wood sticks, cellulose paper, high-N grass, and low-N grass. Mineral N availability in the microcosms was estimated using ion-exchange resin bags. Functional diversity of the microcosms was analyzed through the use of the Biolog-system of sole-C-utilization patterns. Soil respiration was the most sensitive measure of functional changes, with significant decreases observed starting at the 500 mg kg -1 treatment. No differences in N availability were observed across the U treatments. Litter decomposition was significantly decreased at the 25,000 mg kg -1 level relative to the control for all litter types except the high-N grass. Wood decomposition was reduced by 84% at the 25,000 mg kg - treatment, cellulose paper by 68%, and low-N grass by 15%. Decreases in the functional diversity of the bacterial community were related to the observed decrease in soil respiration, and to the greater effect on decomposition of the lower-quality litter types

Topical and working papers on uranium resources and availability

International Nuclear Information System (INIS)

Basic topics relative to world-wide resources and availability of uranium resources; potential for recovery of uranium from mill tailings in Canada; uranium from seawater; depleted uranium as an energy source; world uranium requirements in perspective

Determination of the stoichiometric ratio uranium dioxide samples

International Nuclear Information System (INIS)

Moura, Sergio Carvalho

1999-01-01

The determination of the O/U stoichiometric ratio in uranium dioxide is an important parameter in order to qualify nuclear fuels. The excess oxygen in the crystallographic structure can cause changes in the physico-chemical properties of this compound such as variation of the thermal conductivity alterations, fuel plasticity and others, affecting the efficiency of this material when it is utilized as nuclear fuel in the reactor core. The purpose of this work is to evaluate methods for the determination of uranium oxide samples from two different production processes, using gravimetric, voltammetric and X-ray diffraction techniques. After the evaluation of these techniques, the main aspect of this work is to define a reliable methodology in order to characterize the behavior of uranium oxide. The methodology used in this work consisted of two different steps: utilization of gravimetric and volumetric methods in order to determine the ratio in uranium dioxide samples; utilization of X-ray diffraction technique in order to determine the lattice parameters using patterns and application of the Rietveld method during refining of the structural data. As a result of the experimental part of this work it was found that the X-ray diffraction analysis performs better and detects the presence of more phases than gravimetric and voltammetric techniques, not sensitive enough in this detection. (author)

Difficulties in preparing a standard sample of uranium metal having traces of nitrogen

International Nuclear Information System (INIS)

Toteja, R.S.D.; Jangida, B.L.; Sundaresan, M.

1991-01-01

Normally in the analysis of uranium for nitrogen, the nitrides are hydrolysed to give NH 3 and that for standardisation purposes to approximate the closest conditions of analysis of ammonia, NH 4 Cl is added to the sample and the recovery is tested. An appropriate method will be to have a standard sample of uranium with known amounts of nitrogen to be used as reference sample. The present work describes the efforts made in the preparation of such a reference sample and a general assessment of such methods available. In present work, known microamounts of nitrogen in an enclosed volume were allowed to react at a temperature of 773 K with a fixed amount of uranium metal of nitrogen content determined chemically. As the reaction of nitrogen with uranium is essentially a surface reaction, a sample had to be homogenised by allowing the nitrided sample to melt at about 1500 K and allow the nitrogen to diffuse through so that the concentration gradient along the profile will disappear. Attempts were made to prepare such samples in the range to 40 to 100 ppm of nitrogen. The density differences of uranium nitride and uranium metal made this diffusion and homogenisation process difficult. The prepared samples were analysed by the micro-kjeldahl's method and the recoveries tested. The equipment used for the preparation of the nitrided samples, for homogenisation and analysis of the results obtained are detailed in the paper together with the assessment of the general methods. (author). 2 refs., 1 fig., 1 tab

Laser fluorimetric determination of uranium in environmental samples from Nile Delta and adjacent regions

International Nuclear Information System (INIS)

Shawky, S.; Ibrahiem, N.; Farouk, A.; Ghods, A.

1994-01-01

Total uranium content was determined in soil and plant samples obtained from various areas in the Nile Delta. Samples taken from east and west of the delta, Suez canal cities and from the Alexandria region were analysed using laser fluorimetry (LF). Uranium was extracted from digested samples with methyl-isobutyl ketone and measured using a laser fluorimeter. The radium content of the same soil samples was determined using gamma spectroscopy. The uranium content of plant samples was determined using LF, since this technique has a detection limit lower than that of GS. Uranium content in the samples varied between 0.6-4.4 μg/g for soil and 0.032-0.17 μg/g for plant tissue. (author)

Thermal performance of a depleted uranium shielded storage, transportation, and disposal package

International Nuclear Information System (INIS)

Wix, S.D.; Yoshimura, H.R.

1994-01-01

The US Department of Energy (DOE) is responsible for management and disposal of large quantities of depleted uranium (DU) in the DOE complex. Viable economic options for the use and eventual disposal of the material are needed. One possible option is the use of DU as shielding material for vitrified Defense High-Level Waste (DHLW) storage, transportation, and disposal packages. Use of DU as a shielding material provides the potential benefit of disposing of significant quantities of DU during the DHLW storage and disposal process. Two DU package concepts have been developed by Sandia National Laboratories. The first concept is the Storage/Disposal plus Transportation (S/D+T) package. The S/D+T package consists of two major components: a storage/disposal (S/D) container and a transportation overpack. The second concept is the S/D/T package which is an integral storage, transportation, and disposal package. The package concept considered in this analysis is the S/D+T package with seven DHLW waste canisters

169 Résumé Abstract Measure of uranium in some samples of ...

African Journals Online (AJOL)

youness

puits et par activation neutronique. Mots-clés : Uranium, Radioactivité naturelle, Coraux, Coquilles de mollusques, lichens, travertins, Carbonates. Abstract. Measure of uranium in some samples of natural deposits in Morocco: environmental implications. In this work, we report the measurement results of uranium content in.

Uranium-lead shielding for nuclear material transportation systems

International Nuclear Information System (INIS)

Lusk, E.C.; Miller, N.E.; Basham, S.J. Jr.

1978-01-01

The basis for the selection of shielding materials for spent fuel shipping containers is described with comments concerning the favorable and unfavorable aspects of steel, lead, and depleted uranium. A concept for a new type of material made of depleted uranium and lead is described which capitalizes on the best cask shielding characteristics of both materials. This cask shielding is made by filling the shielding cavity with pieces of depleted uranium and then backfilling the interstitial voids with lead. The lead would be bonded to the uranium and also to the cask shells if desired. Shielding density approaching 80 percent of that of solid uranium could be achieved, while a density of 65 percent is readily obtainable. This material should overcome the problems of the effect of lead melting in the fire accident, high thermal gradients at uranium-stainless steel interfaces and at a major reduction in cost over that of a solid uranium shielded cask. A development program is described to obtain information on the properties of the composite material to aid in design analysis and licensing and to define the fabrication techniques

The effect of sample preparation on uranium hydriding

International Nuclear Information System (INIS)

Banos, A.; Stitt, C.A.; Scott, T.B.

2016-01-01

Highlights: • Distinct differences in uranium hydride growth rates and characteristics between different surface preparation methods. • The primary difference between the categories of sample preparations is the level of strain present in the surface. • Greater surface-strain, leads to higher nucleation number density, implying a preferred attack of strained vs unstrained metal. • As strain is reduced, surface features such as carbides and grain boundaries become more important in controlling the UH3 location. - Abstract: The influence of sample cleaning preparation on the early stages of uranium hydriding has been examined, by using four identical samples but concurrently prepared using four different methods. The samples were reacted together in the same corrosion cell to ensure identical exposure conditions. From the analysis, it was found that the hydride nucleation rate was proportional to the level of strain exhibiting higher number density for the more strained surfaces. Additionally, microstructure of the metal plays a secondary role regarding initial hydrogen attack on the highly strained surfaces yet starts to dominate the system while moving to more pristine samples.

Effects of a diuretic and its combination with chelating agent on the removal of depleted uranium in rats

International Nuclear Information System (INIS)

Ikeda, Mizuyo; Fukuda, Satoshi; Nakamura, Mariko; Yoshida, Hiroki; Yan Xueming; Xie Yuyuan

2008-01-01

We examined the effects of a diuretic, isotonic saline, and chelating agent, catechol-3, 6-bis (methyleimiodiacetic acid) (CBMIDA), on the excretion and prevention of renal damage of depleted uranium (DU). Male Wistar rats (8 weeks old) divided into seven groups were preinjected intraperitoneally with 4 mg/kg DU and then the six groups were injected intraperitoneally with a diuretic, a diuretic plus isotonic saline, 480 mg/kg or 720 mg/kg CBMIDA alone, or 480 mg/kg or 720 mg/kg CBMIDA plus a diuretic and saline for three days, and the one group was as the control (no treatment). The rats were killed 6 days after DU injection. The results indicated that the diuretic alone and the diuretic with isotonic saline were not effective in removing uranium from the body and protecting the renal function, and also did not help to increase significantly the effects of CBMIDA. (author)

Dissolution of metallic uranium and its alloys. Part II. Screening study results: Identification of an effective non-thermal uranium dissolution method

International Nuclear Information System (INIS)

Laue, C.A.; Gates-Anderson, D.; Fitch, T.E.

2004-01-01

Screening experiments were performed to evaluate reagent systems that deactivate pyrophoric, metallic depleted uranium waste streams at ambient temperature. The results presented led to the selection of two systems, which would be investigated further, for the design of the LLNL onsite treatment process of metallic depleted uranium wastes. The two feasible systems are: (a) 7.5 mol/l H 2 SO 4 - 1 mol/l HNO 3 and (b) 3 mol/l HCl - 1 mol/l H 3 PO 4 . The sulfuric acid system dissolves uranium metal completely, while the hydrochloric-phosphoric acid system converts the metal completely into a solid, which might be suitable for direct disposal. Both systems combine oxidation of metallic uranium with complexation of the uranium ions formed to effectively deactivate uranium.s pyrophoricity at ambient temperature. (author)

Fluorimetrich determination of uranium in mineral samples and phosphoric solutions

International Nuclear Information System (INIS)

Pupo Gonzales, I.; Cuevillas, J.; Estevez, J.

1991-01-01

In this paper an analytical technique for the determination of uranium in different cuban minerals and acid leaching liquors of phosphorites is proposed. The method used for solid samples includes their disolution and further dilution of the solution obtained. For liquid samples dilution is the only intermediate step used. A study of HNO3 concentration (pH) was made in fluorimetric measurements. The method was applied to the uranium analysis in two IAEA standard reference samples (phosphate base), in natural phosphorites and a synthetic one, in clays and phosphoric liquors. The results agree with those obtained by other methods

The utilization of uranium industry technology and relevant chemistry to leach uranium from mixed-waste solids

International Nuclear Information System (INIS)

Mattus, A.J.; Farr, L.L.

1991-01-01

Methods for the chemical extraction of uranium from a number of refractory uranium-containing minerals found in nature have been in place and employed by the uranium mining and milling industry for nearly half a century. These same methods, in conjunction with the principles of relevant uranium chemistry, have been employed at the Oak Ridge National Laboratory (ORNL) to chemically leach depleted uranium from mixed-waste sludge and soil. The removal of uranium from what is now classified as mixed waste may result in the reclassification of the waste as hazardous, which may then be delisted. The delisted waste might eventually be disposed of in commercial landfill sites. This paper generally discusses the application of chemical extractive methods to remove depleted uranium from a biodenitrification sludge and a storm sewer soil sediment from the Y-12 weapons plant in Oak Ridge. Some select data obtained from scoping leach tests on these materials are presented along with associated limitations and observations which might be useful to others performing such test work. 6 refs., 2 tabs

The utilization of uranium industry technology and relevant chemistry to leach uranium from mixed-waste solids

Energy Technology Data Exchange (ETDEWEB)

Mattus, A.J.; Farr, L.L.

1991-01-01

Methods for the chemical extraction of uranium from a number of refractory uranium-containing minerals found in nature have been in place and employed by the uranium mining and milling industry for nearly half a century. These same methods, in conjunction with the principles of relevant uranium chemistry, have been employed at the Oak Ridge National Laboratory (ORNL) to chemically leach depleted uranium from mixed-waste sludge and soil. The removal of uranium from what is now classified as mixed waste may result in the reclassification of the waste as hazardous, which may then be delisted. The delisted waste might eventually be disposed of in commercial landfill sites. This paper generally discusses the application of chemical extractive methods to remove depleted uranium from a biodenitrification sludge and a storm sewer soil sediment from the Y-12 weapons plant in Oak Ridge. Some select data obtained from scoping leach tests on these materials are presented along with associated limitations and observations which might be useful to others performing such test work. 6 refs., 2 tabs.

The Possible Effects of Depleted Uranium (DU) Ammunition on the Environment and in Animals

International Nuclear Information System (INIS)

Bozic, T.; Popovic, D.; Stevanovic, J.; Koracevic-Filipovic, M.; Jovic, S.; Todorovic, D.; Radenkovic, M.

2004-01-01

As stated by the official reports, during NATO bombing of Serbia and Montenegro in 1999 approximately 500.000 missiles were used i.e. 3600 kg of uranium oxide, yielding activity of 18,3x1010 Bq entered the environment. Yugoslav Federal Ministry of Defense announced that 8 locations in the region of Vranje, Bujanovac and Lustica Peninsula, outside Kosovo/Metohia, were hit by DU ammunition and were isolated afterwards. The soil was contaminated with 200.000-250.000 Bq uranium/kg soil but this was mainly agricultural land, far from urban areas. The report stated that no DU ammunition was used above 44th parallel. The paper presents the preliminary results of the study on environmental and animal health effects due to the use of DU ammunition during NATO bombing of Serbia and Montenegro in 1999. The samples of animal blood (sheep, caws), soils and vegetation (corps, grass, leaves) were collected randomly in the region of Bujanovac (Novo Selo, Borovac) in the spring/fall of 2003. The hematological and some biochemical parameters of the peripheral blood were analyzed: concentration of hemoglobin, number of erythrocytes, leukocytes, monocytes, lymphocytes, eozinophiles, neutrophiles, serumamiloidA (SAA), haptoglobin (Hp) and malondialdehide in erythrocytes and blood serum. The samples were analyzed by classical manual counting methods, spectrophotometry (by Drapkin) and ELISA immunological technique. Blood samples from the control group of animals on a farm in the vicinity of Belgrade were taken and analyzed for the same parameters, too. The samples of soils and vegetation were dried up and analyzed for the contents of uranium and other natural and man made radionuclides by standard gamma spectrometry (HPGe detector, relative efficiency 23%). The results are to be correlated with the data on the concentration of DU that entered the environment during the bombing, as well as with the data of the long-term measurements of uranium concentrations in the environment and human

Radiological risk assessment of Capstone depleted uranium aerosols.

Science.gov (United States)

Hahn, Fletcher F; Roszell, Laurie E; Daxon, Eric G; Guilmette, Raymond A; Parkhurst, Mary Ann

2009-03-01

Assessment of the health risk from exposure to aerosols of depleted uranium (DU) is an important outcome of the Capstone aerosol studies that established exposure ranges to personnel in armored combat vehicles perforated by DU munitions. Although the radiation exposure from DU is low, there is concern that DU deposited in the body may increase cancer rates. Radiation doses to various organs of the body resulting from the inhalation of DU aerosols measured in the Capstone studies were calculated using International Commission on Radiological Protection (ICRP) models. Organs and tissues with the highest calculated committed equivalent 50-y doses were lung and extrathoracic tissues (nose and nasal passages, pharynx, larynx, mouth, and thoracic lymph nodes). Doses to the bone surface and kidney were about 5 to 10% of the doses to the extrathoracic tissues. Organ-specific risks were estimated using ICRP and U.S. Environmental Protection Agency (EPA) methodologies. Risks for crewmembers and first responders were determined for selected scenarios based on the time interval of exposure and for vehicle and armor type. The lung was the organ with the highest cancer mortality risk, accounting for about 97% of the risks summed from all organs. The highest mean lifetime risk for lung cancer for the scenario with the longest exposure time interval (2 h) was 0.42%. This risk is low compared with the natural or background risk of 7.35%. These risks can be significantly reduced by using an existing ventilation system (if operable) and by reducing personnel time in the vehicle immediately after perforation.

Hydrologic transport of depleted uranium associated with open air dynamic range testing at Los Alamos National Laboratory, New Mexico, and Eglin Air Force Base, Florida

Energy Technology Data Exchange (ETDEWEB)

Becker, N.M. [Los Alamos National Lab., NM (United States); Vanta, E.B. [Wright Laboratory Armament Directorate, Eglin Air Force Base, FL (United States)

1995-05-01

Hydrologic investigations on depleted uranium fate and transport associated with dynamic testing activities were instituted in the 1980`s at Los Alamos National Laboratory and Eglin Air Force Base. At Los Alamos, extensive field watershed investigations of soil, sediment, and especially runoff water were conducted. Eglin conducted field investigations and runoff studies similar to those at Los Alamos at former and active test ranges. Laboratory experiments complemented the field investigations at both installations. Mass balance calculations were performed to quantify the mass of expended uranium which had transported away from firing sites. At Los Alamos, it is estimated that more than 90 percent of the uranium still remains in close proximity to firing sites, which has been corroborated by independent calculations. At Eglin, we estimate that 90 to 95 percent of the uranium remains at test ranges. These data demonstrate that uranium moves slowly via surface water, in both semi-arid (Los Alamos) and humid (Eglin) environments.

Hydrologic transport of depleted uranium associated with open air dynamic range testing at Los Alamos National Laboratory, New Mexico, and Eglin Air Force Base, Florida

International Nuclear Information System (INIS)

Becker, N.M.; Vanta, E.B.

1995-01-01

Hydrologic investigations on depleted uranium fate and transport associated with dynamic testing activities were instituted in the 1980's at Los Alamos National Laboratory and Eglin Air Force Base. At Los Alamos, extensive field watershed investigations of soil, sediment, and especially runoff water were conducted. Eglin conducted field investigations and runoff studies similar to those at Los Alamos at former and active test ranges. Laboratory experiments complemented the field investigations at both installations. Mass balance calculations were performed to quantify the mass of expended uranium which had transported away from firing sites. At Los Alamos, it is estimated that more than 90 percent of the uranium still remains in close proximity to firing sites, which has been corroborated by independent calculations. At Eglin, we estimate that 90 to 95 percent of the uranium remains at test ranges. These data demonstrate that uranium moves slowly via surface water, in both semi-arid (Los Alamos) and humid (Eglin) environments

Uranium management activities

International Nuclear Information System (INIS)

Jackson, D.; Marshall, E.; Sideris, T.; Vasa-Sideris, S.

2001-01-01

One of the missions of the Department of Energy's (DOE) Oak Ridge Office (ORO) has been the management of the Department's uranium materials. This mission has been accomplished through successful integration of ORO's uranium activities with the rest of the DOE complex. Beginning in the 1980's, several of the facilities in that complex have been shut down and are in the decommissioning process. With the end of the Cold War, the shutdown of many other facilities is planned. As a result, inventories of uranium need to be removed from the Department facilities. These inventories include highly enriched uranium (HEU), low enriched uranium (LEU), normal uranium (NU), and depleted uranium (DU). The uranium materials exist in different chemical forms, including metals, oxides, solutions, and gases. Much of the uranium in these inventories is not needed to support national priorities and programs. (author)

A Convenient Method for Estimation of the Isotopic Abundance in Uranium Bearing Samples

International Nuclear Information System (INIS)

AI -Saleh, F.S.; AI-Mukren, Alj.H.; Farouk, M.A.

2008-01-01

A convenient and simple method for estimation of the isotopic abundance in some uranium bearing samples using gamma-ray spectrometry is developed using a hyper pure germanium spectrometer and a standard uranium sample with known isotopic abundance

Report of the panel on the use of depleted uranium alloys for large caliber long rod kinetic energy penetrators

International Nuclear Information System (INIS)

Sandstrom, D.J.; Jessen, N.; Loewenstein, P.; Weirick, L.

1980-01-01

In early 1977 the National Materials Advisory Board, an operating unit in the Commission on Sociotechnical Systems of the National Research Council, NAS/NAE, formed a study committee on High Density Materials for Kinetic Energy Penetrators. The Specific objectives of the Committee were defined as follows. Assess the potential of two materials for use in kinetic energy penetrators, including such factors as: (a) properties (as applied to this application: strength, toughness, and dynamic behavior); (b) uniformity, reliability and reproducibility; (c) deterioration in storage; (d) production capability; (e) ecological impact; (f) quality assurance; (g) availability, and (h) cost. The Committee was divided into two Panels; one panel devoted to the study of tungsten alloys and the other devoted to the study of depleted uranium alloys for use in Kinetic energy penetrators. This report represents the findings and recommendation of the Panel on Uranium

Use of depleted uranium in military conflicts and possible impact on health and environment

International Nuclear Information System (INIS)

Snihs, J.O.; Aakerblom, G.

2000-01-01

There has been concern regarding the possible environmental impacts of depleted uranium (DU) and its possible health effects on both military personnel and on civilians following the Gulf War 1991. These issues have been raised by several non-governmental organizations, some scientists and by a number of press reports. Since DU could also have been used in the Balkan conflict 1999, there has been a concern about the possible consequences of its use for the people and for the environment of this region. Because of this concern it was considered necessary to review existing information on DU and give appropriate recommendations in the aftermath of the Balkans conflict. This was made in October 1999. In November 2000 a Mission to Kosovo was undertaken on basis of new information from NATO

Options for disposal and reapplication of depleted uranium hexafluoride

International Nuclear Information System (INIS)

Fitch, St.H.

2009-01-01

The nuclear renaissance has spurred the need to enrich uranium to fuel power reactors to meet the nation's energy requirements. However, enriching uranium produces the volatile byproduct of DUF 6 tails. In an ambient environment, DUF 6 decomposes into uranium oxides and hydrogen fluoride (HF). This HF component makes DUF 6 unsuitable for disposal as low-level waste. To make DUF 6 suitable for disposal, it must be stabilized in a controlled process by converting it into uranium oxides and fluorine compounds by the processes of de-conversion and fluorine extraction. Once stabilized, the DU and fluorine have reapplication potential that would delay or divert the need for disposal. Certain challenges confound this process, notably the chemical toxicity from elemental fluorine and DU, radiation hazards, limited low-level waste disposal capacity, and potential political and public opposition. (authors)

Results of EDS uranium samples characterization after hydrogen loading

International Nuclear Information System (INIS)

Chicea, D.; Dash, J.

2003-01-01

Several experiments of loading natural uranium foils with hydrogen were done. Electrolysis was used for loading hydrogen into uranium, because it is the most efficient way for H loading. The composition of the surface and near surface of the samples was determined using an Oxford EDS spectrometer on a Scanning Electron Microscope, manufactured by ISI. Images were taken with several magnifications up to 3.4KX. Results reveal that when low current density was used, the surface patterns changed from granules on the surface having a typical size of 2-4 microns to pits under the surface having a typical size under one micron. When high current density was used the surface changed and presented deep fissures. The deep fissures are the result of the mechanical strain induced by the lattice expansion caused by hydrogen absorption. The surface composition was determined before and after hydrogen loading. Uranium, thorium platinum and carbon concentration were measured. Experiments suggest that the amount of thorium increases on the uranium sample with the total electric charge transported through electrolyte. Carbon concentration was found to decrease on the surface of the sample as the total electric charge transported through electrolyte increased. Platinum is used in electrolysis experiment as anode primarily because it does not dissolve in electrolyte and therefore it is not electro-deposited on the cathode surface. The results of the platinum concentration measurements on the surface of the samples we loaded with hydrogen reveal that the platinum concentration increased dramatically as the current density increased and that created platinum spots on the cathode surface. Work is in progress on the subject. (authors)

Normalisation of spot urine samples to 24-h collection for assessment of exposure to uranium

International Nuclear Information System (INIS)

Marco, R.; Katorza, E.; Gonen, R.; German, U.; Tshuva, A.; Pelled, O.; Paz-tal, O.; Adout, A.; Karpas, Z.

2008-01-01

For dose assessment of workers at Nuclear Research Center Negev exposed to natural uranium, spot urine samples are analysed and the results are normalised to 24-h urine excretion based on 'standard' man urine volume of 1.6 l d -1 . In the present work, the urine volume, uranium level and creatinine concentration were determined in two or three 24-h urine collections from 133 male workers (319 samples) and 33 female workers (88 samples). Three volunteers provided urine spot samples from each voiding during a 24-h period and a good correlation was found between the relative level of creatinine and uranium in spot samples collected from the same individual. The results show that normalisation of uranium concentration to creatinine in a spot sample represents the 24-h content of uranium better than normalisation to the standard volume and may be used to reduce the uncertainty of dose assessment based on spot samples. (authors)

Chapter 1. General information about uranium. 1.10. Uranium application

International Nuclear Information System (INIS)

Khakimov, N.; Nazarov, Kh.M.; Mirsaidov, I.U.

2011-01-01

Full text: Metallic uranium or its compounds are used as nuclear fuel in nuclear reactors. A natural or low-enriched admixture of uranium isotopes is applied in stationery reactors of nuclear power plants, and products of a high enrichment degree are used in nuclear power plants or in reactors that operates with fast neutrons. 235 U is a source of nuclear energy in nuclear weapons. Depleted uranium is used as armour-piercing core in bombshells. 238 U serves as a source of secondary nuclear fuel - plutonium. (author)

Chapter 1. General information about uranium. 1.10. Uranium application

International Nuclear Information System (INIS)

Khakimov, N.; Nazarov, Kh.M.; Mirsaidov, I.U.

2012-01-01

Full text: Metallic uranium or its compounds are used as nuclear fuel in nuclear reactors. A natural or low-enriched admixture of uranium isotopes is applied in stationery reactors of nuclear power plants, and products of a high enrichment degree are used in nuclear power plants or in reactors that operates with fast neutrons. 235 U is a source of nuclear energy in nuclear weapons. Depleted uranium is used as armour-piercing core in bombshells. 238 U serves as a source of secondary nuclear fuel - plutonium.

Study on the relation between uranium content and total phosphorus in some sudanese phosphate ore samples

International Nuclear Information System (INIS)

Mohammed, A.A.; Eltayeb, M.A.H.

2003-01-01

In the present work uranium content and total phosphorous were determined in 30 phosphate ore samples collected from Kurun and Uro areas in Nuba mountains in sudan. Spectrophotometry technique was used for this purpose. Uranium analysis is based on the use of nitrogen (V) acid for leaching the rock, and treatment with ammonium carbonate solution, whereby uranium (VI) is kept in solution as its carbonate complex. The ion-exchange technique was used for the recovery of uranium. Uranium was eluted from the resin with 1 M hydrochloric acid. In the elute, uranium was determined spectrophotometrically by measurement of the absorbance of the yellow uranium (VI) - 8- hydroxyquinolate complex at λ 400 nm. The total phosphorus was measured as (P 2 O 5 %) by treatment of the leach liquor with ammonium molybdate solution. The absorbance of the blue complex was measured at λ 880 nm. The results show that a limited relation is existed between uranium content and total phosphorus in phosphate samples from Kurun area, which contain 58.8 ppm uranium in average, where there are no relation is existed in phosphate samples samples from Uro area, which contain 200 ppm uranium in average

Estimation of uranium in different types of water and sand samples by adsorptive stripping voltammetry

International Nuclear Information System (INIS)

Bhalke, Sunil; Raghunath, Radha; Mishra, Suchismita; Suseela, B.; Tripathi, R.M.; Pandit, G.G.; Shukla, V.K.; Puranik, V.D.

2005-01-01

A method is standardized for the estimation of uranium by adsorptive stripping voltammetry using chloranilic acid (CAA) as complexing agent. The optimum parameters to get best sensitivity and good reproducibility for uranium were 60s adsorption time, pH 1.8, chloranilic acid (2x10 -4 M) and 0.002M EDTA. The peak potential under this condition was found to be -0.03 V. With these optimum parameters a sensitivity of 1.19 nA/nM uranium was observed. Detection limit for this optimum parameter was found to be 0.55 nM. This can be further improved by increasing adsorption time. Using this method, uranium was estimated in different type of water samples such as seawater, synthetic seawater, stream water, tap water, well water, bore well water and process water. This method has also been used for estimation of uranium in sand, organic solvent used for extraction of uranium from phosphoric acid and its raffinate. Sample digestion procedures used for estimation of uranium in various matrices are discussed. It has been observed from the analysis that the uranium peak potentials changes with matrix of the sample, hence, standard addition method is the best method to get reliable and accurate results. Quality assurance of the standardized method is verified by analyzing certified reference water sample from USDOE, participating intercomparison exercises and also by estimating uranium content in water samples both by differential pulse adsorptive stripping voltammetric and laser fluorimetric techniques. (author)

Fission blanket benchmark experiment on spherical assembly of uranium and PE with PE reflector

Energy Technology Data Exchange (ETDEWEB)

Zhu, Tonghua; Lu, Xinxin; Wang, Mei; Han, Zijie, E-mail: neutron_integral@aliyun.com; Jiang, Li; Wen, Zhongwei; Liu, Rong

2016-04-15

Highlights: • The fission rate distribution on two depleted uranium assemblies was measured with plate fission chambers. • We do calculations using MCNP code and ENDF/B-V.0 library. • The overestimation of calculations to the measured fission rates was found. • The observed discrepancy are discussed. - Abstract: New concept of fusion-fission hybrid for energy generation has been proposed. To validate the nuclear performance of fission blanket of hybrid, as part of series of validation experiment, two types of fission blanket assemblies were setup in this work and measurements were made of the reaction rate distribution for uranium fission in the spherical assembly of depleted uranium and polyethylene by Plate Fission Chamber (PFC). There are two PFCs in experiment, one is depleted uranium chamber and the other is enriched uranium chamber. The Monte-Carlo transport code MCNP5 and continuous energy cross sections library ENDF/BV.0 were used for the analysis of fission rate distribution in the two types of assemblies. The calculated results were compared with the experimental ones. The overestimation of fission rate for depleted uranium and enriched uranium were found in the inner boundary of the two assemblies. However, the C/E ratio tends to decrease for the distance from the core slightly and the results for enriched uranium are better than that for depleted uranium.

Estimation of uranium isotope in urine samples using extraction chromatography resin

International Nuclear Information System (INIS)

Thakur, Smita S.; Yadav, J.R.; Rao, D.D.

2012-01-01

Internal exposure monitoring for alpha emitting radionuclides is carried out by bioassay samples analysis. For occupational radiation workers handling uranium in reprocessing or fuel fabrication facilities, there exists a possibility of internal exposure and urine assay is the preferred method for monitoring such exposure. Estimation of lower concentration of uranium at mBq level by alpha spectrometry requires preconcentration and its separation from large volume of urine sample. For this purpose, urine samples collected from non radiation workers were spiked with 232 U tracer at mBq level to estimate the chemical yield. Uranium in urine sample was pre-concentrated by calcium phosphate coprecipitation and separated by extraction chromatography resin U/TEVA. In this resin extractant was DAAP (Diamylamylphosphonate) supported on inert Amberlite XAD-7 support material. After co-precipitation, precipitate was centrifuged and dissolved in 10 ml of 1M Al(NO 3 ) 3 prepared in 3M HNO 3 . The sample thus prepared was loaded on extraction chromatography resin, pre-conditioned with 10 ml of 3M HNO 3 . Column was washed with 10 ml of 3M HNO 3 . Column was again rinsed with 5 ml of 9M HCl followed by 20 ml of 0.05 M oxalic acid prepared in 5M HCl to remove interference due to Th and Np if present in the sample. Uranium was eluted from U/TEVA column with 15 ml of 0.01M HCl. The eluted uranium fraction was electrodeposited on stainless steel planchet and counted by alpha spectrometry for 360000 sec. Approximate analysis time involved from sample loading to stripping is 2 hours when compared with the time involved of 3.5 hours by conventional ion exchange method. Seven urine samples from non radiation worker were radio chemically analyzed by this technique and the radiochemical yield was found in the range of 69-91 %. Efficacy of this method against conventional anion exchange technique earlier standardized at this laboratory is also being highlighted. Minimum detectable activity

Uranium Content in the Geological Samples of Different River Valleys in the Dauki fault Belt of Jaintiapur

International Nuclear Information System (INIS)

Chowdhury, Minhaz ul Islam; Ahmed Monir; Bhuiyan Abu Daiyan; Akon Eunus

1996-01-01

Thirty four geological samples that include six radioactive rock samples, four soil samples, two ooze samples,twelve stream-sediment samples and ten water samples, collected during a field survey in Jaintiapur area of the Dauki fault belt, oriented to the study on probable mobility of uranium either as detritus or in aquatic solution through the region, have been investigated with fluorimeter so as to find out content of uranium in the samples. The investigation aims at determining geochemical significance on uranium occurrence prevailing in the area. In general, the content of uranium in the rock samples lies in average distribution of geochemical interest. However, 194 ppm of uranium content in the gross material of the rock sample, collected from Lalakhal anomaly that records 1500 cps in situ, bears geochemical significance. But, the anomaly being associated with a cross -bedding, the presence of uranium may be inferred as an accumulation in placer sediment transported from a nearby source, Despite absence of in situ radiometric anomalies in the overall geological formations other than the Tipam and the Dupitila Sandstone members as encountered in the traverse of Sari valley , the area, in general, appears to be potential for possible occurrence of uranium. The transported stream sediments ooze and surface run-off water, as collected from the Rangapani, the Sari and even the Nayagang show geochemically significant distribution of uranium. Laboratory analyses of soil samples refers to dispersion of U bearing materials in the soil along the major channels.Uranium content in the surface run-off water of the Sari, the Rangapani and the Nayagang that have originated from the uranium bearing Meghalayan hills strongly support previous inference on mobility of uranium in aquatic solution through the geological formations of the area for possible formation of secondary uranium deposits. Eventually, prevailing geological evidences advocate that the area may be brought

Radiological Risk Assessment of Capstone Depleted Uranium Aerosols

International Nuclear Information System (INIS)

Hahn, Fletcher; Roszell, Laurie E.; Daxon, Eric G.; Guilmette, Ray A.; Parkhurst, MaryAnn

2009-01-01

Assessment of the health risk from exposure to aerosols of depleted uranium (DU) is an important outcome of the Capstone aerosol studies that established exposure ranges to personnel in armored combat vehicles perforated by DU munitions. Although the radiation exposure from DU is low, there is concern that DU deposited in the body may increase cancer rates. Radiation doses to various organs of the body resulting from the inhalation of DU aerosols measured in the Capstone studies were calculated using International Commission on Radiological Protection (ICRP) models. Organs and tissues with the highest calculated committed equivalent 50-yr doses were lung and extrathoracic tissues (nose and nasal passages, pharynx, larynx, mouth and thoracic lymph nodes). Doses to the bone surface and kidney were about 5 to 10% of the doses to the extrathoracic tissues. The methodologies of the ICRP International Steering Committee on Radiation Standards (ISCORS) were used for determining the whole body cancer risk. Organ-specific risks were estimated using ICRP and U.S. Environmental Protection Agency (EPA) methodologies. Risks for crew members and first responders were determined for selected scenarios based on the time interval of exposure and for vehicle and armor type. The lung was the organ with the highest cancer mortality risk, accounting for about 97% of the risks summed from all organs. The highest mean lifetime risk for lung cancer for the scenario with the longest exposure time interval (2 h) was 0.42%. This risk is low compared with the natural or background risk of 7.35%. These risks can be significantly reduced by using an existing ventilation system (if operable) and by reducing personnel time in the vehicle immediately after perforation

Molecular, cellular, and tissue impact of depleted uranium on xenobiotic-metabolizing enzymes.

Science.gov (United States)

Gueguen, Yann; Rouas, Caroline; Monin, Audrey; Manens, Line; Stefani, Johanna; Delissen, Olivia; Grison, Stéphane; Dublineau, Isabelle

2014-02-01

Enzymes that metabolize xenobiotics (XME) are well recognized in experimental models as representative indicators of organ detoxification functions and of exposure to toxicants. As several in vivo studies have shown, uranium can alter XME in the rat liver or kidneys after either acute or chronic exposure. To determine how length or level of exposure affects these changes in XME, we continued our investigation of chronic rat exposure to depleted uranium (DU, uranyl nitrate). The first study examined the effect of duration (1-18 months) of chronic exposure to DU, the second evaluated dose dependence, from a level close to that found in the environment near mining sites (0.2 mg/L) to a supra-environmental dose (120 mg/L, 10 times the highest level naturally found in the environment), and the third was an in vitro assessment of whether DU exposure directly affects XME and, in particular, CYP3A. The experimental in vivo models used here demonstrated that CYP3A is the enzyme modified to the greatest extent: high gene expression changed after 6 and 9 months. The most substantial effects were observed in the liver of rats after 9 months of exposure to 120 mg/L of DU: CYP3A gene and protein expression and enzyme activity all decreased by more than 40 %. Nonetheless, no direct effect of DU by itself was observed after in vitro exposure of rat microsomal preparations, HepG2 cells, or human primary hepatocytes. Overall, these results probably indicate the occurrence of regulatory or adaptive mechanisms that could explain the indirect effect observed in vivo after chronic exposure.

CHANGES OF INDICATORS OF THE PERIPHERAL BLOOD AND HAEMOPOIESIS AT INKORPORATION OF THE DEPLETED URANIUM IN THE EXPERIMENT

Directory of Open Access Journals (Sweden)

D. V. Gerasimov

2011-01-01

Full Text Available In article is considered the experiment with incorporation of the solution of the mixed oxides of the depleted uranium to laboratory animals (the rats and following the cytological study of the peripheral blood and marrow after influence. The changes of indicators of the peripheral blood and haemopoiesis of experimental animals are indicative of the effort processes of indemnification, that shows depleted uranium’s radioactive and toxicological effects and insolvency of natural protective mechanisms of the organism. The results of the research have shown that changes of the haemopoiesis were ambiguous. There was shown the oppression myeloid haemopoiesis and leukopenia to the third month of the experiment. In same time existed the increase an erythroid parts of hemopoiesis. The parameters of the peripheral blood and haemopoiesis to completion of the experiment did not reach checking importances that points to practicability of the long observation for animal after one-shot influence with DU.

Radium 226 and uranium isotopes simultaneously determination in water samples using liquid scintillation counter

International Nuclear Information System (INIS)

Al-Masri, M.S.; Al-Akel, B.; Saaid, S.; Nashawati, A.

2007-04-01

In this work a method has been developed to determine simultaneously Radium 226 and Uranium isotopes in water samples by low back ground Liquid Scintillation Counter. Radium 226 was determined by its progeny Polonium 214 after one month of sample storage in order to achieve the equilibrium between Radium 226 and Polonium 214. Uranium isotopes were determined by subtracting Radium 226 activity from total alpha activity. The method detection limits were 0.049 Bq/L and 0.176 Bq/L for Radium 226 and Uranium isotopes respectively. The repeatability limits were ± 0.32 Bq/L and ± 0.9 Bq/L for Radium 226 and Uranium isotopes respectively. While relative errors were % 9.5 and %18.2 for Radium 226 and Uranium isotopes respectively. On the other hand, the report presented the results of different standard and natural samples.(author)

Manual for the sampling of uranium mine tailings

International Nuclear Information System (INIS)

Feenstra, S.; Reades, D.W.; Cherry, J.A.; Chambers, D.B.; Case, G.G.; Ibbotson, B.G.

1983-04-01

The purpose of this manual is to describe the requisite sampling procedures to provide a basis for the application of uniform high-quality standards to detailed geotechnical, hydrogeological, geochemical and air quality measurements at Canadian uranium tailings disposal sites. The report describes the objective and scope of a sampling program, the preliminary data collection, and the procedures for sampling of tailings solids, surface water and seepage, tailings porewater, and wind-blown dust and radon

Analysis of a Uranium Oxide Sample Interdicted in Slovakia (FSC 12-3-1)

Energy Technology Data Exchange (ETDEWEB)

Borg, Lars E. [Lawrence Livermore National Lab. (LLNL), Livermore, CA (United States); Dai, Zurong [Lawrence Livermore National Lab. (LLNL), Livermore, CA (United States); Eppich, Gary R. [Lawrence Livermore National Lab. (LLNL), Livermore, CA (United States); Gaffney, Amy M. [Lawrence Livermore National Lab. (LLNL), Livermore, CA (United States); Genetti, Victoria G. [Lawrence Livermore National Lab. (LLNL), Livermore, CA (United States); Grant, Patrick M. [Lawrence Livermore National Lab. (LLNL), Livermore, CA (United States); Gray, Leonard W. [Lawrence Livermore National Lab. (LLNL), Livermore, CA (United States); Holiday, Kiel S. [Lawrence Livermore National Lab. (LLNL), Livermore, CA (United States); Hutcheon, Ian D. [Lawrence Livermore National Lab. (LLNL), Livermore, CA (United States); Kayzar, Theresa M. [Lawrence Livermore National Lab. (LLNL), Livermore, CA (United States); Klunder, Gregory L. [Lawrence Livermore National Lab. (LLNL), Livermore, CA (United States); Knight, Kimberly B. [Lawrence Livermore National Lab. (LLNL), Livermore, CA (United States); Kristo, Michael J. [Lawrence Livermore National Lab. (LLNL), Livermore, CA (United States); Lindvall, Rachel E. [Lawrence Livermore National Lab. (LLNL), Livermore, CA (United States); Marks, Naomi E. [Lawrence Livermore National Lab. (LLNL), Livermore, CA (United States); Ramon, Christina E. [Lawrence Livermore National Lab. (LLNL), Livermore, CA (United States); Ramon, Erick C. [Lawrence Livermore National Lab. (LLNL), Livermore, CA (United States); Robel, Martin [Lawrence Livermore National Lab. (LLNL), Livermore, CA (United States); Roberts, Sarah K. [Lawrence Livermore National Lab. (LLNL), Livermore, CA (United States); Schorzman, Kerri C. [Lawrence Livermore National Lab. (LLNL), Livermore, CA (United States); Sharp, Michael A. [Lawrence Livermore National Lab. (LLNL), Livermore, CA (United States); Singleton, Michael J. [Lawrence Livermore National Lab. (LLNL), Livermore, CA (United States); Williams, Ross W. [Lawrence Livermore National Lab. (LLNL), Livermore, CA (United States)

2014-01-17

We provide a concise summary of analyses of a natural uranium sample seized in Slovakia in November 2007. Results are presented for compound identification, water content, U assay, trace element abundances, trace organic compounds, isotope compositions for U, Pb, Sr and O, and age determination using the ²³⁴U – ²³⁰Th and ²³⁵U – ²³¹Pa chronometers. The sample is a mixture of two common uranium compounds - schoepite and uraninite. The uranium isotope composition is indistinguishable from natural; ²³⁶U was not detected. The O, Sr and Pb isotope compositions and trace element abundances are unremarkable. The ²³⁴U – ²³⁰Th chronometer gives an age of 15.5 years relative to the date of analysis, indicating the sample was produced in January 1997. A comparison of the data for this sample with data in the Uranium Sourcing database failed to find a match, indicating the sample was not produced at a facility represented in the database.

Study of uranium plating measurement

International Nuclear Information System (INIS)

Lin Jufang; Wen Zhongwei; Wang Mei; Wang Dalun; Liu Rong; Jiang Li; Lu Xinxin

2007-06-01

In neutron physics experiments, the measurement for plate-thickness of uranium can directly affect uncertainties of experiment results. To measure the plate-thickness of transform target (enriched uranium plating and depleted uranium plating), the back to back ionization chamber, small solid angle device and Au-Si surface barrier semi-conductor, were used in the experiment study. Also, the uncertainties in the experiment were analyzed. Because the inhomo-geneous of uranium lay of plate can quantitively affect the result, the homogeneity of uranium lay is checked, the experiment result reflects the homogeneity of uranium lay is good. (authors)

Metallothionein deficiency aggravates depleted uranium-induced nephrotoxicity

Energy Technology Data Exchange (ETDEWEB)

Hao, Yuhui; Huang, Jiawei; Gu, Ying; Liu, Cong; Li, Hong; Liu, Jing; Ren, Jiong; Yang, Zhangyou [State Key Laboratory of Trauma, Burns and Combined Injury, Institute of Combined Injury, Chongqing Engineering Research Center for Nanomedicine, College of Preventive Medicine, Third Military Medical University, No. 30 Gaotanyan Street, Shapingba District, Chongqing 400038 (China); Peng, Shuangqing [Evaluation and Research Center for Toxicology, Institute of Disease Control and Prevention, Academy of Military Medical Science, 20 Dongdajie Street, Fengtai District, Beijing 100071 (China); Wang, Weidong, E-mail: wwdwyl@sina.com [Department of Radiation Oncology, Shanghai Jiao Tong University Affiliated Sixth People' s Hospital, Shanghai 200233 (China); Li, Rong, E-mail: yuhui_hao@126.com [State Key Laboratory of Trauma, Burns and Combined Injury, Institute of Combined Injury, Chongqing Engineering Research Center for Nanomedicine, College of Preventive Medicine, Third Military Medical University, No. 30 Gaotanyan Street, Shapingba District, Chongqing 400038 (China)

2015-09-15

Depleted uranium (DU) has been widely used in both civilian and military activities, and the kidney is the main target organ of DU during acute high-dose exposures. In this study, the nephrotoxicity caused by DU in metallothionein-1/2-null mice (MT −/−) and corresponding wild-type (MT +/+) mice was investigated to determine any associations with MT. Each MT −/− or MT +/+ mouse was pretreated with a single dose of DU (10 mg/kg, intraperitoneal injection) or an equivalent volume of saline. After 4 days of DU administration, kidney changes were assessed. After DU exposure, serum creatinine and serum urea nitrogen in MT −/− mice significantly increased than in MT +/+ mice, with more severe kidney pathological damage. Moreover, catalase and superoxide dismutase (SOD) decreased, and generation of reactive oxygen species and malondialdehyde increased in MT −/− mice. The apoptosis rate in MT −/− mice significantly increased, with a significant increase in both Bax and caspase 3 and a decrease in Bcl-2. Furthermore, sodium-glucose cotransporter (SGLT) and sodium-phosphate cotransporter (NaPi-II) were significantly reduced after DU exposure, and the change of SGLT was more evident in MT −/− mice. Finally, exogenous MT was used to evaluate the correlation between kidney changes induced by DU and MT doses in MT −/− mice. The results showed that, the pathological damage and cell apoptosis decreased, and SOD and SGLT levels increased with increasing dose of MT. In conclusion, MT deficiency aggravated DU-induced nephrotoxicity, and the molecular mechanisms appeared to be related to the increased oxidative stress and apoptosis, and decreased SGLT expression. - Highlights: • MT −/− and MT +/+ mice were used to evaluate nephrotoxicity of DU. • Renal damage was more evident in the MT −/− mice after exposure to DU. • Exogenous MT also protects against DU-induced nephrotoxicity. • MT deficiency induced more ROS and apoptosis after exposure to

Metallothionein deficiency aggravates depleted uranium-induced nephrotoxicity

International Nuclear Information System (INIS)

Hao, Yuhui; Huang, Jiawei; Gu, Ying; Liu, Cong; Li, Hong; Liu, Jing; Ren, Jiong; Yang, Zhangyou; Peng, Shuangqing; Wang, Weidong; Li, Rong

2015-01-01

Depleted uranium (DU) has been widely used in both civilian and military activities, and the kidney is the main target organ of DU during acute high-dose exposures. In this study, the nephrotoxicity caused by DU in metallothionein-1/2-null mice (MT −/−) and corresponding wild-type (MT +/+) mice was investigated to determine any associations with MT. Each MT −/− or MT +/+ mouse was pretreated with a single dose of DU (10 mg/kg, intraperitoneal injection) or an equivalent volume of saline. After 4 days of DU administration, kidney changes were assessed. After DU exposure, serum creatinine and serum urea nitrogen in MT −/− mice significantly increased than in MT +/+ mice, with more severe kidney pathological damage. Moreover, catalase and superoxide dismutase (SOD) decreased, and generation of reactive oxygen species and malondialdehyde increased in MT −/− mice. The apoptosis rate in MT −/− mice significantly increased, with a significant increase in both Bax and caspase 3 and a decrease in Bcl-2. Furthermore, sodium-glucose cotransporter (SGLT) and sodium-phosphate cotransporter (NaPi-II) were significantly reduced after DU exposure, and the change of SGLT was more evident in MT −/− mice. Finally, exogenous MT was used to evaluate the correlation between kidney changes induced by DU and MT doses in MT −/− mice. The results showed that, the pathological damage and cell apoptosis decreased, and SOD and SGLT levels increased with increasing dose of MT. In conclusion, MT deficiency aggravated DU-induced nephrotoxicity, and the molecular mechanisms appeared to be related to the increased oxidative stress and apoptosis, and decreased SGLT expression. - Highlights: • MT −/− and MT +/+ mice were used to evaluate nephrotoxicity of DU. • Renal damage was more evident in the MT −/− mice after exposure to DU. • Exogenous MT also protects against DU-induced nephrotoxicity. • MT deficiency induced more ROS and apoptosis after exposure to

The influence of the addition of depleted uranium on particle pushing in melt-processed, bulk Y-Ba-Cu-O

International Nuclear Information System (INIS)

Diko, P; Zmorayova, K; Babu, N Hari; Krabbes, G; Cardwell, D A

2004-01-01

The microstructure of single-grain, melt-processed (MP) YBa 2 Cu 3 O 7 /Y 2 BaCuO 5 (Y-123/Y-211) samples (YBCO) containing varying amounts of depleted uranium (DU) and Pt has been studied. Only partial refinement of the Y-211 particle size was observed in Pt-free samples, which generally contained both small and large Y-211 particles. Small Y-211 particles in these samples are pushed extensively in the c-growth sector (c-GS) and all Y-211 particles (small and large) coarsen with the distance from the seed and with increasing DU concentration. Samples fabricated with Pt contained only very fine Y-211 particles, which were generally pushed strongly in the c-GS. In this case the size of the Y-211 particles did not vary significantly with distance from the seed. U- and U/Pt-containing sub-micron sized particles present in the melt-processed YBCO microstructure were not pushed during solidification, although their arrangement within the structure of the sample was influenced clearly by the growth process. The so-called cyclic growth was observed in the c-GS at the highest DU concentration (0.8 wt%). In these samples, this growth pattern is associated with the formation of a liquid phase rich in U and Y at the growth front. The cyclic growth mechanism was modified by the addition of Pt. Crystals of Y 2 Ba 4 UCuO x with Ba 3 YUO x phase inclusions were observed to be present in the U/Y-rich melt

Maximizing percentage depletion in solid minerals

International Nuclear Information System (INIS)

Tripp, J.; Grove, H.D.; McGrath, M.

1982-01-01

This article develops a strategy for maximizing percentage depletion deductions when extracting uranium or other solid minerals. The goal is to avoid losing percentage depletion deductions by staying below the 50% limitation on taxable income from the property. The article is divided into two major sections. The first section is comprised of depletion calculations that illustrate the problem and corresponding solutions. The last section deals with the feasibility of applying the strategy and complying with the Internal Revenue Code and appropriate regulations. Three separate strategies or appropriate situations are developed and illustrated. 13 references, 3 figures, 7 tables

Influence of depleted uranium on hepatic cholesterol metabolism in apolipoprotein E-deficient mice.

Science.gov (United States)

Souidi, M; Racine, R; Grandcolas, L; Grison, S; Stefani, J; Gourmelon, P; Lestaevel, P

2012-04-01

Depleted uranium (DU) is uranium with a lower content of the fissile isotope U-235 than natural uranium. It is a radioelement and a waste product from the enrichment process of natural uranium. Because of its very high density, it is used in the civil industry and for military purposes. DU exposure can affect many vital systems in the human body, because in addition to being weakly radioactive, uranium is a toxic metal. It should be emphasized that, to be exposed to radiation from DU, you have to eat, drink, or breathe it, or get it on your skin. This particular study is focusing on the health effects of DU for the cholesterol metabolism. Previous studies on the same issue have shown that the cholesterol metabolism was modulated at molecular level in the liver of laboratory rodents contaminated for nine months with DU. However, this modulation was not correlated with some effects at organs or body levels. It was therefore decided to use a "pathological model" such as hypercholesterolemic apolipoprotein E-deficient laboratory mice in order to try to clarify the situation. The purpose of the present study is to assess the effects of a chronic ingestion (during 3 months) of a low level DU-supplemented water (20 mg L(-1)) on the above mentioned mice in order to determine a possible contamination effect. Afterwards the cholesterol metabolism was studied in the liver especially focused on the gene expressions of cholesterol-catabolising enzymes (CYP7A1, CYP27A1 and CYP7B1), as well as those of associated nuclear receptors (LXRα, FXR, PPARα, and SREBP 2). In addition, mRNA levels of other enzymes of interest were measured (ACAT 2, as well as HMGCoA Reductase and HMGCoA Synthase). The gene expression study was completed with SRB1 and LDLr, apolipoproteins A1 and B and membrane transporters ABC A1, ABC G5. The major effect induced by a low level of DU contamination in apo-E deficient mice was a decrease in hepatic gene expression of the enzyme CYP7B1 (-23%) and nuclear

Trace uranium analysis in Indian coal samples using the fission track technique

International Nuclear Information System (INIS)

Jojo, P.J.; Rawat, A.; Kumar, Ashavani; Prasad, Rajendra

1993-01-01

The ever-growing demand for energy has resulted in the extensive use of fossil fuels, especially coal, for power generation. Coal and its by-products often contain significant amounts of radionuclides, including uranium, which is the ultimate source of the radioactive gas Radon-222. The present study gives the concentration of uranium in coal samples of different collieries in India, collected from various thermal power plants in the state of Uttar Pradesh. The estimates were made using the fission track technique. Latent damage tracks were not found to be uniformly distributed but showed sun bursts and clusters. Non-uniform distributions of trace elements are a very common phenomenon in rocks. The levels of uranium in the coal samples were found to vary from 2.0 to 4.9 ppm in uniform distributions and from 21.3 to 41.0 ppm in non-uniform distributions. Measurements were also made on fly ash samples where the average uranium concentration was found to be 8.4 and 49.3 ppm in uniform and non-uniform distributions, respectively. (author)

Metallography of pitted aluminum-clad, depleted uranium fuel

International Nuclear Information System (INIS)

Nelson, D.Z.; Howell, J.P.

1994-01-01

The storage of aluminum-clad fuel and target materials in the L-Disassembly Basin at the Savannah River Site for more than 5 years has resulted in extensive pitting corrosion of these materials. In many cases the pitting corrosion of the aluminum clad has penetrated in the uranium metal core, resulting in the release of plutonium, uranium, cesium-137, and other fission product activity to the basin water. In an effort to characterize the extent of corrosion of the Mark 31A target slugs, two unirradiated slug assemblies were removed from basin storage and sent to the Savannah River Technology Center for evaluation. This paper presents the results of the metallography and photographic documentation of this evaluation. The metallography confirmed that pitting depths varied, with the deepest pit found to be about 0.12 inches (3.05 nun). Less than 2% of the aluminum cladding was found to be breached resulting in less than 5% of the uranium surface area being affected by corrosion. The overall integrity of the target slug remained intact

Hydrogeochemical and stream sediment sampling for uranium in the sandstone environment

International Nuclear Information System (INIS)

Wenrich, K.J.

1985-01-01

Sandstone terranes commonly host uranium occurrences in the western United States. In addition, because sedimentary terranes, particularly shales and immature, not well cemented sandstone, contribute more sediment and soluble material than do plutonic, volcanic, or metamorphic terranes they are an excellent regime for hydrogeochemical and stream-sediment prospecting. Because of higher conductivity, and hence higher uranium content, of waters draining such environments the sampling need not be as precise nor the analytical detection limit as low as in other terranes to yield a successful survey. Nevertheless, reasonable preparation and care of the samples is recommended: (1) The water samples should be filtered through 0.45 μm membranes and acidified to a pH of less than 1. (2) Because the adsorption of uranium by organic material is so significant it is recommended that the reasonable finest stream-sediment fraction, 4 , conductivity, etc.) are useful in the data reduction towards the elimination of false anomalies. (author)