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Sample records for 106ru 141ce 144ce

  1. An experimental study of the time dependence of uptake from soil of 137Cs, 106Ru, 144Ce and 99Tc into green vegetables, wheat and potatoes

    In this study the experimental data were analysed using the CEGB's dynamic foodchain model, and were used to validate the relevant part of the model structure, to produce model-specific input data and to identify possible future improvements to the model structure. The root uptake of the specified radionuclides was studied and the concentration levels measured. The data were analysed using a simplified version of the general model. The compartment system incorporated within the model was shown to be capable of reproducing the data for 137Cs, 106Ru and 144Ce to an extent sufficient to justify its use in ingestion radiological dose assessments, but to be less successful in fitting the 99Tc data. The analysis resulted in the production of a well validated set of model-specific input data relevant to UK conditions and agricultural practice differing significantly from values obtained from global literature surveys. Possible future improvements to the model structure were also identified, aimed at providing improved estimates of crop contamination levels for timescales in excess of those considered in this study. (U.K.)

  2. Chromatographic isolation of 144Ce and 144Pr from the wastes of irradiated uranium treatment

    A two-step chromatographic technique was elaborated to isolate 144Ce, 144Pr from a solution of uranium fission products in 6M HNO3. The oxidation to Ce(III) by bromate and selective adsorption of 144Ce(IV) on anion exchange column were used to concentrate and purify 144Ce. Some impurities of uranium, 95Zr, 95Nb, 106Ru remain in 144Ce solution after the first step of its isolation. The final purification is achieved by passing the 6M HNO3 solution of 144Ce(IV) through the HDEHP-coated teflon column. The decontamination factors of 144Ce from main fission products are given. 7.2 mCi of (144Ce+144Pr) are recovered from each gram of irradiated uranium trioxide with the yield greater than 99%. An improvement of known generator was carried out to elute a purer 144Pr from maternal 144Ce(IV) adsorbed on the anion exchange column. (author)

  3. A new 144Ce/144Pr radioisotope generator system

    A miniaturized generator system was developed containing manganese dioxide-coated alumina on which 144Ce is deposited and from which 144Pr is eluted with an aqueous solution of 1% KIO3 in 1 N nitric acid. More than 60% of the 144Pr was recovered with a 99.9% radionuclide purity even after 2000 ml eluant and 1000 1 or air had been passed through the column. (author)

  4. Absolute standardization of 106Ru by anti-coincidence method

    The system of absolute standardization activity of radionuclide by anti-coincidence counting and live-time techniques was implemented at LNMRI in 2008 to reduce the impacts of some influence factors in the determination of the activity with coincidence counting technique used for decades in the lab, for example, the measurement time. With the anti-coincidence system, the variety of radionuclides that can be calibrated by LNMRI was increased, in relation to the type of decay. The objective of this work is the standardization of 106Ru by the method of counting anti-coincidence and estimate its measurement uncertainties. (author)

  5. β-Ray brachytherapy with 106Ru plaques for retinoblastoma

    Purpose: A retrospective analysis of 134 patients who received 106Ru brachytherapy for retinoblastomas (175 tumors in 140 eyes). Treatment and follow-up were analyzed with special emphasis on tumor control organ, preservation, and late complications. Results: Treated tumors had a mean height and diameter of 3.7 ± 1.4 mm and 5.0 ± 2.8 disk diameters, respectively. The radiation dose values were recalculated according to the calibration standard recently introduced by the National Institute of Standards and Technology. The recalculation revealed a mean applied dose of 419 Gy at the sclera (SD, 207 Gy) and 138 Gy (SD, 67 Gy) at the tumor apex. The 5-year tumor control rate was 94.4%. Tumor recurrence was more frequent in eyes with vitreous tumor cell seeding or fish-flesh regression. The estimated 5-year eye preservation rate was 86.5%. Previous treatment by brachytherapy or external beam radiotherapy, as well as a large tumor diameter, were significant factors for enucleation. The radiotherapy-induced complications after 5 years of follow-up were retinopathy (22%), optic neuropathy (21%), and cataract (17%). These complications were significantly more frequent after prior brachytherapy or external beam radiotherapy. Conclusion: Brachytherapy using 106Ru plaques is a highly efficient therapy with excellent local tumor control and an acceptable incidence of side effects

  6. Toxicity of 144Ce inhaled in a relatively insoluble form by immature beagle dogs. VI

    Immature Beagle dogs (approximately equal to 3 months of age at exposure) have been exposed by inhalation to a relatively insoluble form of 144Ce (in fused aluminosilicate particles) to compare the resulting patterns of metabolism, dosimetry and biological effects with those seen in dogs exposed at 12 and 14 months of age and at 8 to 10.5 years of age. Five blocks of longevity animals, each consisting of 10 exposed dogs and one control, are currently on experiment. The initial lung burdens of the 144Ce-exposed dogs range from 0.004 to 140 μCi 144Ce/kg body weight. Three dogs with initial lung burdens of 73 to 120 μCi 144Ce/kg body weight died at 66 to 121 days after exposure with pulmonary injury and congestive heart failure. One dog with an initial lung burden of 140 μCi 144Ce/kg body weight died at 91 days after exposure with severe radiation pneumonitis and minimal pulmonary fibrosis and another dog whose initial lung burden was 70 μCi 144Ce/kg body weight died at 511 days after exposure with pulmonary injury that was mainly fibrotic in nature. Two dogs with initial lung burdens of 52 and 64 μCi 144Ce/kg body weight had primary pulmonary hemangiosarcomas and died at 618 and 689 days, respectively, with cumulative average absorbed beta doses to lung of 23,000 and 29,000 rads. One dog with an initial lung burden of 28 μCi 144Ce/kg body weight was euthanized at 1227 days after exposure with a hemangiosarcoma of the mediastinum, and another dog with an initial lung burden of 12 μCi 144Ce/kg body weight died at 1520 days after exposure from epilepsy. Serial observations are continuing on the surviving 40 exposed and five control dogs

  7. Transfer from soil to plants of 106Ru as nitrosyl and as chloride

    The transfer of 106Ru in a soil-plant ecosystem was investigated with respect to two chemical forms in compact soil samples under greenhouse conditions with surface and deep-layer contamination. Considerable differences in the uptake of 106Ru were observed between 106RuCl3 and 106Ru-nitrosyl during the first 5-8 wk after the contamination of the soil. The translocation of 106Ru in the soil showed an inhomogeneous distribution of the radioruthenium, with a great part of the total activity remaining in the upper soil layer between 0 and 5 cm even 10 mo after contamination of the soil surface. During the whole experiment, reemission of 106Ru into the air was investigated by using special air collectors under different temperature and light conditions. Although a continuous checking out for a time of about 8 mo, no measurable concentrations of 106Ru could be out for a time of about 8 mo, no measurable concentrations of 106Ru could be found in examined air filters

  8. Clinical quality assurance for 106Ru ophthalmic applicators

    Background and purpose: Episcleral brachytherapy using 106Ru/106Rh ophthalmic applicators is a proven method of therapy of uveal melanomas sparing the globe and in many cases sparing the vision. In the year 2001, an internal clinical quality assurance procedure revealed that part of the ophthalmic applicators leaked and that the calibration was erroneous. Consequently, the producer modernized its production procedures and, in May 2002, introduced a dose rate calibration that is traceable to the NIST standard. This NIST calibration confirmed that the previous calibration had been incorrect. In order to study the effects of the producer's new internal quality assurance procedures on the ophthalmic applicators, applicators of this new generation were submitted to a newly improved internal clinical acceptance test. Patients and methods: The internal clinical acceptance test consists of a leakage test and a dosimetric test of the ophthalmic applicators. The leakage test simulates contact of the ophthalmic applicators with chloride containing body fluid. The dosimetric tests measure depth dose curves and dose rate with a plastic scintillator dosimetric system and compare them with the indications in the producer's certificate. Furthermore, the depth dose profile of the most frequently used applicator (type CCB) was compared with published data. Results: The internal clinical leakage test showed that all of the tested ophthalmic applicators belonging to the new generation (n=17) were tight and not contaminated. The dosimetric acceptance tests applied to seven different types of applicators revealed that the relative depth dose profiles in the therapeutically relevant range (up to a depth of ≤7 mm) deviate from the producer's indications only by -2.7 to +3.2%. The acceptance test of the dose rate values of the ophthalmic applicators at a distance of 2 mm from the surface of the applicators resulted in a coefficient of variation of 1.7% (n=17). In the evaluation of the

  9. Toxicity of 144Ce inhaled in a relatively insoluble form by immature Beagle dogs. XVII

    Immature Beagle dogs (3-mo old) received a single, brief inhalation exposure to 144Ce in fused aluminosilicate particles as part of a series of studies designed to study the effects of age on dose response relationships for inhaled radionuclides. Forty-nine dogs inhaled graded levels of 144Ce that resulted in initial lung burdens ranging from 0.004-140 μCi/kg 0.15-5200 kBq/kg) body weight. Five control dogs inhaled nonradioactive fused aluminosilicate particles. Forty-one of the 144Ce-exposed dogs have died: 11 with lung tumors 4 with tumors of the tracheobronchial lymph nodes, with a nasal cavity tumor, and 9 with non neoplastic diseases of the respiratory tract. Observations are continuing on the 8 144Ce-exposed dogs that are surviving at this time. (author)

  10. Toxicity of inhaled 144CeCl3 in beagle dogs. VIII

    Studies on the metabolism, dosimetry, and effects of inhaled 144CeCl3 in the Beagle dog are continuing to provide information that will aid in assessing the biological consequences of inhaling 144Ce such as might be released in certain nuclear accidents. Studies on the tissue distribution of inhaled 144CeCl3 have shown that the 144Ce deposited in lung is translocated at a moderately rapid rate to liver and skeleton and that significant radiation doses are accumulated by all three organs. Fifty-five dogs that inhaled 144CeCl3 and 15 control dogs were placed in a longevity study and are being observed for their lifespan. The 144Ce dogs had long-term retained burdens with values ranging from 20 to 2900 μCi. Thirty-one of the dogs exposed to 144CeCl3 have died; 8 at 21 to 44 days after inhalation with signs attributed to severe bone marrow damage and associated pancytopenia; 2 at 138 and 144 days with radiation pneumonitis; 3 at 309 to 874 days with hepatic necrosis; 1 at 510 days with marrow aplasia; 1 at 375 days with pulmonary fibrosis; and 16 at 799 to 3081 days, most with neoplasms or myeloproliferative disorders. In this last group, 1 dog had an osteosarcoma, 3 had squamous cell carcinomas of the maxilla, 2 of the latter also having primary pulmonary neoplasms, 5 had hemangiosarcomas of the liver, 1 had a hemangiosarcoma of the nasal cavity, 2 had myelogenous leukemia, 1 had myelofibrosis with myeloid metaplasia, 1 had spinal cord ependymomas, and 2 did not have neoplasms. One of these had severe myelomalacia and the other diffuse hepatic lipidosis with severe degeneration. Two controls died; 1 with a thyroid carcinoma and 1 with aspiration pneumonia. Serial observations are continuing on the 24 surviving 144CeCl3 dogs and 13 control dogs. (U.S.)

  11. Toxicity of inhaled 144CeCl3 in beagle dogs. XI

    Studies on the metabolism, dosimetry and effects of inhaled 144CeCl3 in Beagle dogs are being conducted to assess the biological consequences of inhaling 144Ce such as might be released in certain nuclear accidents. Studies on the organ distribution of inhaled 144CeCl3 have shown that the 144Ce deposited in the lung is translocated at a moderately rapid rate to liver and skeleton and that significant radiation doses are accumulated by all three organs. Fifty-five dogs that inhaled 144CeCl3 and 15 control dogs are being observed for their life span. The 144Ce dogs have long-term retained burdens with values ranging from 20 to 2900 μCi. Forty-five of the dogs exposed to 144CeCl3 have died; eight from 21 to 44 days after inhalation with severe bone marrow damage and associated pancytopenia; two at 138 and 144 days with radiation pneumonitis; three from 309 to 874 days with hepatic necrosis; one at 510 days with marrow aplasia; one at 375 days with pulmonary fibrosis; and 30 from 799 to 4085 days, most with neoplasms or myeloproliferative disorders. In this last group, one dog had an osteosarcoma, five had squamous cell carcinomas of the nasal cavity (two also having primary pulmonary neoplasms), six had hemangiosarcomas of the liver, one had a hemangiosarcoma of the nasal cavity, two had myelogenous leukemia, one had myelofibrosis with myeloid metaplasia, one had spinal cord ependymomas, one had a malignant melanoma (also an ependymoma) and two had mammary adenocarcinomas. Three dogs had primary pulmonary neoplasms including two with bronchogenic adenocarcinomas and one with an adenoma. Seven did not have malignant neoplasms. Two of these had severe myelomalacia, one had pulmonary edema, three had congestive heart failure and one had diffuse hepatic lipidosis with severe hepatic degeneration

  12. Inter-taxa differences in root uptake of 103/106Ru by plants

    Ruthenium-106 is of potential radioecological importance but soil-to-plant Transfer Factors for it are available only for few plant species. A Residual Maximum Likelihood (REML) procedure was used to construct a database of relative 103/106Ru concentrations in 114 species of flowering plants including 106 species from experiments and 12 species from the literature (with 4 species in both). An Analysis of Variance (ANOVA), coded using a recent phylogeny for flowering plants, was used to identify a significant phylogenetic effect on relative mean 103/106Ru concentrations in flowering plants. There were differences of 2465-fold in the concentration to which plant species took up 103/106Ru. Thirty-nine percent of the variance in inter-species differences could be ascribed to the taxonomic level of Order or above. Plants in the Orders Geraniales and Asterales had notably high uptake of 103/106Ru compared to other plant groups. Plants on the Commelinoid monocot clades, and especially the Poaceae, had notably low uptake of 103/106Ru. These data demonstrate that plant species are not independent units for 103/106Ru concentrations but are linked through phylogeny. It is concluded that models of soil-to-plant transfer of 103/106Ru should assume that; neither soil variables alone affect transfer nor plant species are independent units, and taking account of plant phylogeny might aid predictions of soil-to-plant transfer of 103/106Ru, especially for species for which Transfer Factors are not available

  13. Toxicity of 144Ce inhaled in a relatively insoluble form by aged Beagle dogs. XII

    The toxicity of relatively insoluble 144Ce inhaled by 8- to 10.5-year-old Beagle dogs is being investigated to determine possible age-related differences in long-term biological responses. Forty-two dogs were exposed to aerosols of 144Ce in fused aluminosilicate particles to yield initial lung burdens of 2.2 to 75 μCi 144Ce/kg body weight, and 12 control dogs were exposed to non-radioactive fused aluminosilicate particles. All 144Ce-exposed and control dogs have died or were euthanized between 197 and 2726 days after the inhalation exposure. Prominent findings in the 144Ce-exposed dogs were radiation pneumonitis in 19 of the 23 dogs that died during the first 943 days after exposure, and neoplastic disease in 13 of the 20 dogs that died beyond 904 days after exposure. Pulmonary tumors were found in five of these dogs. In contrast to the study with young adult dogs, in which pulmonary hemangiosarcomas were one of the prominent findings, all of these tumors were carcinomas

  14. Toxicity of 144Ce inhaled in a relatively insoluble form by immature Beagle dogs. XII

    Immature Beagle dogs (3 months old) were exposed once by inhalation to an aerosol of 144Ce incorporated in fused aluminosilicate particles. The influence of this age on the dose-response relationships is being compared to that of 13-mo-old and 8 to 10.5-yr-old dogs. This study involves 49 dogs that received graded initial lung burdens from 0.004 to 140 μCi 144Ce/kg body weight and five control dogs. To date, 19 of the 144Ce-exposed dogs and one of the controls have died. Dogs with the highest initial lung burdens of 144Ce died during the first 4 months with radiation pneumonitis, pulmonary fibrosis, and congestive heart failure. Pulmonary hemangiosarcoma was the primary finding in dogs that died at 1.5 to 2 years after exposure. Deaths beyond that time have been due primarily to extrapulmonary hemangiosarcomas. Observations are continued on the surviving 30 144Ce-exposed and four control dogs at 7.0 to 11.2 years after exposure

  15. Toxicity of inhaled 144Ce in fused aluminosilicate particles in aged beagle dogs. V

    The toxicity of 144Ce in fused aluminosilicate particles inhaled by 8- to 10.5-yr-old dogs is being investigated to provide information on age-related differences in the response of older members of the human population to accidental inhalation of radioactive aerosols. These data on aged dogs will be compared to the results of similar studies of dogs exposed at approximately 3 mo or 12 to 14 mo of age. Six blocks of five female dogs each have been divided into four exposure levels with mean initial lung burdens of 7.2, 14, 28 and 57 μCi 144Ce/kg body weight. Six blocks of four male dogs have been divided into three exposure levels with mean initial lung burdens of 7.2, 14 and 28 μCi 144Ce/kg body weight. Controls in each block were exposed to fused aluminosilicate particles containing stable cerium. Fifteen dogs with initial lung burdens ranging from 20 to 75 μCi 144Ce/kg body weight and cumulative doses to lung of from 22,000 to 74,000 rads have died or were euthanized 197 to 1207 days after exposure with clinicopathologic findings of radiation pneumonitis and pulmonary fibrosis.Pulmonary retention of the inhaled 144Ce was similar to that observed previously in dogs exposed at 18 to 22 mo of age in a radiation dose pattern study. Serial observations are continuing on the 19 surviving 144Ce-exposed and eight control dogs

  16. Toxicity of 144Ce fused clay particles inhaled by aged dogs. III

    The toxicity of 144Ce fused clay particles inhaled by 8- to 10.5-year-old dogs is being investigated to provide information on age-related differences in the response of older members of the human population to accidental inhalation of radioactive aerosols. These data on aged dogs will be compared to the results of similar studies using dogs exposed at approximately 3 months or 12 to 14 months of age. To date, 7 blocks of 5 dogs each, divided into 4 exposure levels with mean initial lung burdens of 7.5, 14, 24, and 57 μCi/kg body weight and control dogs exposed to non-labeled fused clay particles have been entered into a longevity study. Twelve dogs with initial lung burdens ranging from 20 to 75 μCi 144Ce/kg body weight and cumulative doses to lung of from 22,000 to 74,000 rads have died at 197 to 943 days post-inhalation with clinico-pathologic findings of radiation pneumonitis and pulmonary fibrosis. Two of these also had congestive heart failure. In addition, 4 dogs with ILBs of 8 to 14 μCi 144Ce/kg body weight have died of mammary neoplasms or congestive heart failure but without radiation pneumonitis. One dog with an ILB of 9 μCi 144Ce/kg body weight died with a chronic interstitial foreign body pneumonia. Two control dogs have died, one with a mammary carcinoma and one with pyometra. Pulmonary retention of the inhaled 144Ce was similar to that observed previously in dogs exposed at 18 to 22 months of age in a radiation dose pattern study. Serial observations are continuing on the 11 surviving 144Ce-exposed dogs and 5 controls. (U.S.)

  17. Toxicity of 144Ce inhaled in a relatively insoluble form by immature Beagle dogs. VIII

    The influence of age at exposure on the resulting patterns of deposition, retention, dosimetry and biological effects from a single inhalation exposure to a relatively insoluble form of a beta-emitting radionuclide with a relatively long physical half-life is being investigated. Immature Beagle dogs (3 months of age) have been exposed once, by inhalation, to an aerosol of 144Ce incorporated in fused aluminosilicate particles. Eighteen of these dogs were serially sacrificed to study the patterns of deposition, retention and dosimetry and the remaining 49 dogs received graded initial lung burdens that ranged from 0.004 to 140 μCi 144Ce/kg body weight and are being observed over their life span for study of the resulting long-term biological effects. Five control dogs are also included in this study. To date, 13 of the 144Ce-exposed dogs in the longevity study and none of the controls have died. Dogs with the highest initial lung burdens of 144Ce died first (during the first 4 months) with radiation pneumonitis, pulmonary fibrosis and congestive heart failure. Pulmonary hemangiosarcoma was the primary finding in dogs that died at 1.5 to 2 years after exposure. Deaths beyond that time have primarily involved extrapulmonary hemangiosarcomas. One dog, 627B, with an initial lung burden of 24 μCi 144Ce/kg body weight died during the past year at 2341 days after exposure with a widely disseminated hemangiosarcoma showing heavy involvement of the liver and skin. Observations are continuing on the surviving 36 144Ce-exposed and five control dogs

  18. Toxicity of 144Ce inhaled in a relatively insoluble form by aged beagle dogs. VI

    The toxicity of 144Ce inhaled in fused aluminosilicate particles by 8 to 10.5-year-old dogs is being investigated to provide information on age-related differences in the response of older members of the human population to accidental inhalation of radioactive aerosols. These data on aged dogs will be compared to the results of similar studies of dogs exposed at approximately 3 months or 12 to 14 months of age. Six blocks of five female dogs each have been divided into four exposure levels with mean initial lung burdens of 7.2, 14, 28 and 57 μCi 144Ce/kg body weight. Six blocks of four male dogs each have been divided into three exposure levels with mean initial lung burdens of 7.2, 14 and 28 μCi 144Ce/kg body weight. Controls in each block were exposed to fused aluminosilicate particles containing stable cerium. Eighteen dogs with initial lung burdens ranging from 14 to 75 μCi 144Ce/kg body weight and cumulative doses to lung of from 22,000 to 74,000 rads have died or were euthanized 197 to 1207 days after exposure with clinicopathologic findings of radiation pneumonitis and pulmonary fibrosis

  19. Effect of 144Ce inhaled in fused clay particles on the tracheobronchial lymph nodes

    Tracheobronchial lymph node changes and lymphopenia are sequelae to inhalation of relatively insoluble radioactive aerosols by Beagle dogs. To assess the development of these lesions, tracheobronchial lymph nodes from dogs that inhaled 144Ce in fused clay particles were examined at intervals from 2 to 730 days after exposure. Initial lung burdens in the dogs studied ranged from 33 to 63 μCi/kg body weight. The concentration of radioisotope in the tracheobronchial lymph nodes increased during the first year after exposure and exceeded that in the lung about 100 days after exposure. Autoradiographs of the lymph nodes showed that 144Ce particles were present in macrophages in the paracortical zone two days after exposure and that concentrations continued to increase in the paracortical zone and medullary cords. Histologic changes in the nodes included atrophy of the germinal centers and lymphocytic follicles, loss of lymphocytes and accumulation of macrophages in the paracortical zone, accumulation of pigment and isotope-laden macrophages in the medullary cords, occasional infiltrates of neutrophils in the medullary cords and, at later time periods, focal fibrosis of the medullary cords. Tracheobronchial lymph node weights of the dogs exposed to 144Ce in fused clay were not decreased until 512 days after exposure. These findings indicate that tracheobronchial lymph nodes accumulate relatively high burdens of 144Ce after inhalation of 144Ce in a relatively insoluble form and that the pathologic changes resulting from these burdens are basically atrophic in nature. Primary neoplasms in lymph nodes have not been observed in dogs with initial lung burdens from 0.0024 to over 30 μCi/kg body weight followed for up to 2000 days post-exposure. At the higher levels, however, a high incidence of primary pulmonary neoplasia has been observed. (U.S.)

  20. Study on the characteristics of indigenously developed 106Ru/106Rh source

    A pilot study was initiated to investigate the characteristics of 106Ru/106Rh source for the purpose of inducting it in Quality Assurance programme of personnel monitoring by Bhabha Atomic Research Centre. Towards this goal, a prototype 106Ru/106Rh source was fabricated indigenously. Different parameters such as activity, gamma ray spectrum, beam uniformity, percentage depth dose, output of the source, contribution of gamma and beta components of the source were studied. The detectors used in the study are CaSO4:Dy Teflon disc, pocket dosimeter, HPGe detector and radiochromic films. - Highlights: • Indigenous development of 106Ru/106Rh source for QA in personnel monitoring. • Source parameters such as activity of the source, gamma spectrum were studied. • Dosimetric parameters such as beam uniformity, BSF, gamma and beta contribution and PDD were studied. • TLDs, EBT radiochromic film, HPGe and electronic pocket dosimeter were used in the study

  1. Numerical calculation of relative dose rates from spherical 106Ru beta sources used in ophthalmic brachytherapy

    Eduardo de Paiva

    2015-01-01

    Full Text Available Concave beta sources of 106Ru/106Rh are used in radiotherapy to treat ophthalmic tumors. However, a problem that arises is the difficult determination of absorbed dose distributions around such sources mainly because of the small range of the electrons and the steep dose gradients. In this sense, numerical methods have been developed to calculate the dose distributions around the beta applicators. In this work a simple code in Fortran language is developed to estimate the dose rates along the central axis of 106Ru/106Rh curved plaques by numerical integration of the beta point source function and results are compared with other calculated data.

  2. Numerical calculation of relative dose rates from spherical 106Ru beta sources used in ophthalmic brachytherapy

    de Paiva, Eduardo

    Concave beta sources of 106Ru/106Rh are used in radiotherapy to treat ophthalmic tumors. However, a problem that arises is the difficult determination of absorbed dose distributions around such sources mainly because of the small range of the electrons and the steep dose gradients. In this sense, numerical methods have been developed to calculate the dose distributions around the beta applicators. In this work a simple code in Fortran language is developed to estimate the dose rates along the central axis of 106Ru/106Rh curved plaques by numerical integration of the beta point source function and results are compared with other calculated data.

  3. Toxicity of 144Ce inhaled in a relatively insoluble form by immature Beagle dogs. VII

    Immature Beagle dogs (approx. = 3 months of age at exposure) have been exposed by inhalation to a relatively insoluble form of 144Ce (in fused aluminosilicate particles) to compare the resulting patterns of metabolism, dosimetry and biological effects with those seen in dogs exposed at 12 and 14 months of age and at 8 to 10.5 years of age. Five blocks of longevity animals, each consisting of 10 exposed dogs and one control, are currently being studied. The initial lung burdens of the 144Ce-exposed dogs range from 0.004 to 140 μCi 144Ce/kg body weight. Three dogs with initial lung burdens of 73 to 120 μCi 144Ce/kg body weight died at 66 to 121 days after exposure with pulmonary injury and congestive heart failure. One dog with an initial lung burden of 140 μCi 144Ce/kg body weight died at 91 days after exposure with severe radiation pneumonitis and minimal pulmonary fibrosis and another dog whose initial lung burden was 70 μCi 144Ce/kg body weight died at 511 days after exposure with pulmonary injury that was mainly fibrotic in nature. Four dogs with initial lung burdens of 52 to 79 μCi/kg body weight had primary pulmonary hemangiosarcomas and died between 618 and 738 days, with cumulative average absorbed beta doses to lung of 23,000 to 31,000 rads. Two of these dogs, 1027S and 1024D, died within the past year. One dog with an initial lung burden of 28 μCi/kg body weight was euthanized at 1227 days after exposure with an hemangiosarcoma of the mediastinum. Within the past year, Dog 627S, with an initial lung burden of 48 μCi/kg body weight, died 1732 days after exposure with hemangiosarcoma primary in the liver or spleen. A dog with an initial lung burden of 12 μCi/kg body weight died from epilepsy at 1520 days after exposure. Serial observations are continuing on the surviving 37 exposed and five control dogs

  4. Toxicity of inhaled 144Ce fused clay particles in beagle dogs. VII

    The metabolism, dosimetry, and effects of inhaled 144Ce in fused clay particles are being investigated in the Beagle dog to aid in assessing the biological consequences of release of 144Ce in a relatively insoluble form such as might occur in certain types of nuclear accidents. The toxicity of inhaled 144Ce fused clay is also of general interest since it is representative of intermediate-lived beta-emitting radionuclides. Two major studies with young adult dogs (12 to 14 months of age at exposure) are involved: (1) a metabolism and dosimetry study in which 24 dogs were serially sacrificed over an extended period of time, and (2) a longevity study with 2 series of dogs; Series I with 15 dogs exposed to aerosols of 144Ce in fused clay particles to yield initial lung burdens of 11 to 210 μCi/kg body weight and 3 control dogs exposed to nonradioactive fused clay particles and Series II with 96 dogs exposed to aerosols of 144Ce in fused clay particles to yield initial lung burdens of 0.0024 to 66 μCi/kg body weight and 12 control dogs exposed to nonradioactive fused clay particles. Twenty-eight dogs died or were euthanized at 143 to 2396 days after inhalation of 144Ce. The prominent findings were radiation pneumonitis in 17 dogs that died or were euthanized at early time periods and neoplastic disease in 10 of the 11 dogs that died or were euthanized at 750 days or later; 5 with hemangiosarcoma of the lung, 1 with both a hemangiosarcoma and a fibrosarcoma of the lung, 1 with both a bronchiolo-alveolar carcinoma and a hemangiosarcoma of lung, 1 with a hemangiosarcoma of lung, bronchiolo-alveolar carcinoma, and a bronchiogenic adenocarcinoma, and 1 each with a hemangiosarcoma of the mediastinum and of the spleen. The cumulative radiation dose to the lung at time of death has ranged from 22,000 to 140,000 rads. Serial observations are continuing on the 83 survivors and 15 controls. (U.S.)

  5. Shortcomings of the industrial quality assurance of 106Ru ophthalmic plaques

    Background: Beta emitting 106Ru applicators manufactured by Bebig GmbH (Berlin, Germany) are widely used to treat intraocular tumors. The applicators are fixed to the bulbus and removed after several days. The following therapy relevant defects have been detected by an internal clinical acceptance test: risk of leakage and inconsistent dose-rate specifications by the manufacturer. In the meantime, components of the internal clinical acceptance test have been adopted successfully by the manufacturer of the 106Ru ophthalmic plaques. Material and Method: 106Ru ophthalmic plaques were tested with the following internal clinical acceptance tests: visual inspection, surface contamination, leakage, and dose-rate verification. The surface contamination test consists of a wet wipe test at moderate pressure. For the leakage test of the 106Ru ophthalmic plaques a clinically relevant scenario was developed in which the contact of the applicator with human tissue is simulated. In the course of it the applicator is inserted into Ringer's solution for several days. The certified energy dose-rate statements of the manufacturer are examined with a 1 mm3 plastic scintillator for consistency. (orig.)

  6. Internal clinical acceptance test of the dose rate of 106Ru/106Rh ophthalmic applicators

    For the last forty years or so, episcleral brachytherapy using 106Ru/106Rh ophthalmic applicators has been a proven method of therapy for uveal melanomas, sparing the globe and in many cases conserving the vision. In episcleral brachytherapy, a radioactive 106Ru/106Rh ophthalmic applicator (BEBIG Co., Berlin, Germany) is temporarily fixed on the surface of the bulbus oculi, whereby the intraocular tumour gets irradiated protractedly through the sclera. 106Ru/106Rh ophthalmic applicators are primarily beta sources, i.e. they generate a local dose escalation both in the vessels supplying the tumour and in the tumour itself, while simultaneously sparing the risk structures. In its certificates, BEBIG, the manufacturer of the product, indicates a dose rate for the 106Ru/106Rh ophthalmic applicators at a dose specification reference point which ensures traceability to the NIST standard (12/2001). The dose specification reference point is situated at a distance of 2 mm from the middle of the inner (concave) surface of the applicators, and the dose rate was measured with a scintillation detector (diameter 1 mm, height 0.5 mm). The manufacturer indicates for this dose rate at the dose specification reference point a relative measurement uncertainty of ±20% within the 95% confidence interval. Since the introduction of the NIST calibration, the quality of the calibration passed on by BEBIG to the user has been examined for n=45 ophthalmic applicators

  7. Extraction of carrier-free 144Ce with acetylacetone and 8-hydroxyquinoline

    The extraction of carrier-free 144Ce with 3.25 to 0.65 M solutions of acetylacetone in carbon tetrachloride and with 1.0 to 0.01 M solutions of 8-hydroxyquinoline in chloroform at a constant as well as variable pH was investigated. On the basis of the analysis of distribution curves it may be presumed that in both extraction systems the oxidation of cerium(III) to cerium(IV) microamounts takes place. The distribution curves of extraction and reextraction in the systems with 8-hydroxyquinoline show a considerable complexity. In the extraction system with acetylacetone constants were found which satisfactorily express the distribution of 144Ce in this system. (author)

  8. Biological effects of repeated exposure of beagle dogs to relatively insoluble aerosols of 144Ce. IV

    This experiment is being conducted to study the behavior and long-term biological effects in Beagle dogs of 144Ce inhaled in fused aluminosilicate particles in repeated inhalation exposures for comparison with similar data from dogs that were exposed only once to a similar aerosol. Four groups of nine dogs each were exposed once every eight weeks for two years (13 exposures) to achieve specified exposure goals. The 144Ce-exposed dogs received increasing or relatively constant beta radiation dose rates in contrast to the steadily decreasing dose rate seen after a single inhalation exposure. Exposures in the first and second groups were planned to yield a cumulative absorbed dose to lung of approximately equal to 35,000 rads and those in the third group approximately equal to 17,000 rads within two years after the first exposure. Singly exposed dogs that had died with pulmonary tumors when this experiment was initiated had cumulative doses to death of 29,000 to 61,000 rads. All 13 exposures have been completed. One dog in the 4.5-μCi 144Ce/kg body weight group died at 771 days after first exposure with emaciation, adrenal cortical degeneration and bone marrow aplasia. One control dog died accidentally during anesthesia. During the past year, two additional dogs have died. One dog in the repeated 2.5-μCi 144Ce/kg body weight group died at 1256 days after the first exposure with radiation pneumonitis and pulmonary fibrosis and a control dog died at 1052 days with autoimmune hemolytic anemia. The remaining 32 dogs appear to be in good physical condition except for a persistent lymphopenia at approximately equal to 4 years after the first exposure. They are being maintained for life span observations

  9. The uptake of 90Sr, 137Cs and 144Ce by leaves of spring wheat and rape

    The distribution and accumulation of 90Sr, 137Cs, 144Ce through the leaf surface into the plant have been studied. The results show that the uptake rate of 137Cs by crop plant is about 53%, while the uptake rate for 90Sr and 144Ce is about 0.4%. However 90Sr is absorbed in significant amount from soil whereas 137Cs is absorbed in negligible amount

  10. Internal Clinical Acceptance Test of the Dose Rate of 106Ru/106Rh Ophthalmic Applicators

    Episcleral brachytherapy using 106Ru/106Rh ophthalmic applicators is a proven method of therapy for uveal melanomas, sparing the globe and in many cases, conserving vision. In its certificates, Bebig, the manufacturer of the product, indicates a dose rate for the 106Ru/106Rh ophthalmic applicators which ensures traceability to the NIST standard (12/2001). Since the introduction of the NIST calibration, the quality of the calibration provided by Bebig to the clinical user has been examined for 45 ophthalmic applicators with a plastic scintillator measurement system. Of these, 20 ophthalmic applicators had a dose rate at the dose specification reference point that exceeded the dose rate stated in the manufacturer's certificate by up to 23%. (author)

  11. Influence of chelation therapy (DTPA) on 141Ce retention in rats

    We investigated the influence of oral and parenteral administration of chelation therapy on the retention of 141Ce in young rats. Opposite to results obtained in adult rats present results show high efficacy of oral chelation therapy in reducing radiocerium retention in the whole body and organs of suckling rats. (author) 3 refs

  12. Liver tumors in Beagle dogs exposed by inhalation to 144CeCl3

    Primary malignant hepatic neoplasms developed in 9 of 55 Beagle dogs (16 percent) exposed to 144CeCl3 in CsCl aerosol (seven primary hepatic hemangiosarcomas, one hepatocellular carcinoma and one intrahepatic bile duct carcinoma). Cerium-144 was rapidly translocated from the lung to the liver and skeleton; the liver received the highest cumulative beta dose. The latent periods of hepatic hemangiosarcomas appeared to be dose-related; death from hepatic hemangiosarcoma occurred earlier in dogs which received higher beta doses

  13. Development of a phantom and assessment of (141)Ce as a surrogate radionuclide for flood field uniformity testing of gamma cameras.

    Saxena, Sanjay Kumar; Kumar, Yogendra; Malpani, Basant; Rakshit, Sutapa; Dash, Ashutosh

    2016-06-01

    This paper describes an indigenous method for development and deployment of rechargeable liquid filled phantom with newly proposed radionuclide (141)Ce for determination of extrinsic uniformity of gamma cameras. Details about design of phantom, neutron irradiation of cerium targets, chemical processing of (141)Ce, charging of phantom with (141)Ce solution and their performance evaluation are presented. Suitability of (141)Ce in quality assurance of gamma cameras used in in-vivo diagnostic imaging procedures has been amply demonstrated. PMID:27031297

  14. K-shell ionization in the beta decay of 141Ce

    The total K-shell ionization probability accompanying the β- decay of 141Ce to the 0.145-MeV level in 141Pr was determined to be (1.79 +- 0.11) x 10-4 from Pr Kα x rays in coincidence with the 0.145-MeV gamma ray. This result is in very good agreement with the theoretical calculations of Law and Suzuki

  15. Biological effects of repeated inhalation exposure of Beagle dogs to relatively insoluble aerosols of 144Ce. V

    The behavior and long-term biological effects in Beagle dogs of 144Ce inhaled in fused aluminosilicate particles in repeated inhalation exposures are being studied for comparison with data from dogs that were exposed only once to a similar aerosol. Four groups of nine dogs each were exposed once every 8 weeks for 2 years (13 exposures) to achieve specified exposure goals. These goals were: to increase the lung burden by 2.5 μCi 144Ce/kg body weight with each exposure in the first group; to reestablish lung burdens of 9 or 4.5 μCi 144Ce/kg body weight in the second and third groups, respectively; and to expose controls (fourth group) to fused aluminosilicate particles containing stable cerium. With these exposure sequences, the 144Ce-exposed dogs received increasing or relatively constant beta radiation dose rates in contrast to the steadily decreasing dose rate seen after a single inhalation exposure. Exposures in the first and second groups were planned to yield a cumulative absorbed dose to lung of approx. = 35,000 rads and those in the third group approx. = 17,000 rads within two years after the first exposure. All 13 exposures have been completed. During the past year, one dog in the 9.0 μCi 144Ce/kg body weight group died at 1558 days after the first exposure with autoimmune hemolytic anemia. The remaining 24 144Ce-exposed and seven control dogs generally appear to be in good physical condition with exception of a persistent lymphopenia at approx. = 5 years after the first exposure. They are continuing to be maintained for life span observations

  16. Effects of inhaled 144Ce on cardiopulmonary function and histopathology of the dog

    Twelve dogs inhaled single doses of relatively insoluble particles containing 144Ce and six dogs inhaled particles containing stable cerium as controls. Pulmonary function, clinical, and radiographic evaluations were performed serially. The dogs developed progressive radiation pneumonitis and pulmonary fibrosis similar to that previously reported for whole-lung irradiation from internal or external sources. Focal histologic changes in bronchioles and alveoli were detected functionally during treadmill and tube-breathing stresses at a time when the dogs' clinical and radiographic appearances were normal. Moderate functional impairment was associated with more severe inflammatory and proliferative changes in airways and alveoli. Severe impairment resulted from progressive fibrosis and scarring. These were several strong correlations between functional indices and histological scores. There was a nonlinear relationship between cumulative radiation dose and effects, and once the functional alterations became clinically evident, the disease progressed with little further increase in dose

  17. On the actual state of industrial quality assurance procedures with regard to 106Ru ophthalmic plaques

    In the year 2002, Bebig updated, among other things, the ASMW (GDR) calibration of the dose rate of the 106Ru ophthalmic plaques from the years 1987-1989 by a calibration of the NIST (USA). The current NIST calibration, together with the new equipment for the measurement of the depth dose curves, led to the consequence that the new NIST 2001 dose rate values show, in the mean, a deviation of 0.75 times (plaque type CCC) up to 2.06 times (plaque types CCX, CCY, and CCZ) compared to the dose rate values that had been indicated so far in Bebig's certificate, based on the ASMW 1987 calibration. For the 95% confidence interval, Bebig estimated the measurement uncertainty to be ± 25%. If one takes into consideration the minimal and maximal values in such 95% confidence intervals, it follows that the new NIST 2001 dose rate values deviate between 0.56 times (plaque type CCC) and 2.58 times (plaque types CCX, CCY, and CCZ) from the Bebig certificate (ASMW calibration 1987). As regards leakage, no objections arose in the case of the 106Ru ophthalmic plaques produced according to the new quality standards. (orig.)

  18. Biological effects of repeated inhalation exposure of beagle dogs to aerosols of 144Ce in fused clay particles I

    This experiment was initiated to study the biological behavior and long-term effects of repeated inhalation exposures to 144Ce in fused clay particles compared with those seen in Beagle dogs that received a single exposure as young adults. The 36 dogs, divided into four equal groups, are exposed every 8 weeks to achieve the following: to maintain lung burdens of 9 and 4.5 μCi 144Ce/kg body weight in the first and second groups, respectively; to increase the lung burden by 2.5 μCi 144Ce/kg body weight in the third group with each exposure and to expose controls (fourth group) to fused clay containing stable cerium. With these exposure sequences, the 144Ce-exposed dogs will receive increasing or maintained β dose rates in contrast to the steadily decreasing dose rate seen after a single inhalation exposure. Exposures to the first and third groups will produce a cumulative absorbed dose to lung of approximately equal to 35,000 rads and those to the second group will yield approximately equal to 17,000 rads within 2 yr after the first exposure. Single exposure dogs that had died with pulmonary neoplasia when this experiment was initiated had cumulative doses to death of 29,000 to 61,000 rads. Six of the planned 13 exposures have been completed to date. All exposed dogs are surviving and will be maintained for lifespan observation. (U.S.)

  19. Assessment, modelization and analysis of 106 Ru experimental transfers through a freshwater trophic system

    Experiments are carried out in order to study 106 RU transfers through a freshwater ecosystem including 2 abiotic compartments (water and sediment) and 3 trophic levels (10 species). Experimental results are expressed mathematically so as they can be included into a global model which is then tested in two different situations. The comparison of the available data concerning the in situ measured concentrations to the corresponding calculated ones validates the whole procedure. Analysis of the so validated results lightens ruthenium distribution process in the environment. The rare detection of this radionuclide in organisms living in areas contaminated by known meaningful releases can be explained by a relativity high detection limit and by a slight role of the sediment as a secondary contamination source. (author). 78 figs., 18 tabs

  20. Responses of different dosemeters in beta dosimetry of 106Ru/106Rh ophthalmic applicators

    This work presents the TL response of three kinds of dosimeters from different manufacturing characteristics under irradiation of 106 Ru / 106 Rh sealed sources used in ophthalmic brachytherapy. They are: Ca SO4:Dy + teflon (D- Ca SO4:Dy -0,4), LiF:Mg, Ti (TLD-100) and Ca SO4:Dy (TLD-900). Some of reports accepted by scientific community (NCS report 14 e ICRU report 72) as reference in the quality control of beta applicators dosimetry recommend that the absorbed dose standard uncertainties can be kept below 20%. The TLD Ca SO4:Dy + teflon presented proper sensibility and high precision comparing with the others. Considering the similar dimensions of ophthalmic tumors and aside critical structures it is relevant to reduce undesirable effects due to the irradiation of these structures. Therefore, the quality control in the beta dosimetry using this kind of source is a constant challenge. (author)

  1. Monte Carlo calculation of dose to water of a 106Ru COB-type ophthalmic plaque

    The concave eye applicators with 106Ru/106Rh or 90Sr/90Y beta-ray sources are worldwide used in brachytherapy for treating intraocular tumors. It raises the need to know the exact dose delivered by beta radiation to tumors but measurement of the dose to water (or tissue) is very difficult due to short range of electrons. The Monte Carlo technique provides a powerful tool for calculation of the dose and dose distributions which helps to predict and determine the doses from different shapes of various types of eye applicators more accurately. The Monte Carlo code MCNPX has been used to calculate dose distributions from a COB-type 106Ru/106Rh ophthalmic applicator manufactured by Eckert and Ziegler BEBIG GmbH. This type of a concave eye applicator has a cut-out whose purpose is to protect the eye nerve which makes the dose distribution more complicated. Several calculations have been performed including depth dose along the applicator central axis and various dose distributions. The depth dose along the applicator central axis and the dose distribution on a spherical surface 1 mm above the plaque inner surface have been compared with measurement data provided by the manufacturer. For distances from 0.5 to 4 mm above the surface, the agreement was within 2.5% and from 5 mm the difference increased from 6% up to 25% at 10 mm whereas the uncertainty on manufacturer data is 20% (2s). It is assumed that the difference is caused by nonuniformly distributed radioactivity over the applicator radioactive layer

  2. Accurate estimation of dose distributions inside an eye irradiated with 106Ru plaques

    Background: Irradiation of intraocular tumors requires dedicated techniques, such as brachytherapy with 106Ru plaques. The currently available treatment planning system relies on the assumption that the eye is a homogeneous water sphere and on simplified radiation transport physics. However, accurate dose distributions and their assessment demand better models for both the eye and the physics. Methods: The Monte Carlo code PENELOPE, conveniently adapted to simulate the beta decay of 106Ru over 106Rh into 106Pd, was used to simulate radiation transport based on a computerized tomography scan of a patient's eye. A detailed geometrical description of two plaques (models CCA and CCB) from the manufacturer BEBIG was embedded in the computerized tomography scan. Results: The simulations were firstly validated by comparison with experimental results in a water phantom. Dose maps were computed for three plaque locations on the eyeball. From these maps, isodose curves and cumulative dose-volume histograms in the eye and for the structures at risk were assessed. For example, it was observed that a 4-mm anterior displacement with respect to a posterior placement of a CCA plaque for treating a posterior tumor would reduce from 40 to 0% the volume of the optic disc receiving more than 80 Gy. Such a small difference in anatomical position leads to a change in the dose that is crucial for side effects, especially with respect to visual acuity. The radiation oncologist has to bring these large changes in absorbed dose in the structures at risk to the attention of the surgeon, especially when the plaque has to be positioned close to relevant tissues. Conclusion: The detailed geometry of an eye plaque in computerized and segmented tomography of a realistic patient phantom was simulated accurately. Dose-volume histograms for relevant anatomical structures of the eye and the orbit were obtained with unprecedented accuracy. This represents an important step toward an optimized

  3. Effect on canine lymphocyte function of 144Ce inhaled in fused clay particles

    Beagle dogs exposed by inhalation to 144Ce in fused clay particles develop a persistent lymphopenia and the remaining peripheral lymphocytes in these dogs show a depressed in vitro response to plant mitogens. These studies were designed to evaluate the cellular basis for this defect. The survival and growth of lymphocytes from irradiated and control dogs were evaluated through 96 hours of culture. Many irradiated lymphocytes that were viable in vivo died within 24 hours in vitro. The remaining lymphocytes appeared to grow normally indicating that the early in vitro death was responsible for at least a portion of the difference between irradiated and control lymphocyte cultures. A second experiment was designed to determine if any humoral factors in plasma of irradiated dogs were responsible for the poor response of the lymphocytes. Lymphocytes from irradiated and control dogs were grown with plasma from both types of animals. Heterologous plasma had no apparent effect on lymphocyte growth, indicating that humoral factors were not involved. (U.S.)

  4. Effect of fasting on the transit time of 144Ce in the mouse gut

    Our work with G.I. absorption of actinide elements indicates greater absorption by fasted animals than by animals on regular diets (Weiss and Walburg, undated). Residence time of a metallic compound in the gut may be an important factor influencing G.I. absorption. Cerium-144 (III) chloride was administered by gavage to fasted mice and to mice on regular feed. The G.I. tract was excised, cut into sections, and the activity of each section determined as a function of time after dosing. Our results indicate rapid transit of 144CeCl3 along the empty mouse gut. One hour after dosing, about half the Ce is in the cecal contents; about 40% remains in stomach contents. Twelve hours after dosing, only about 2% remains in the cecum; by 16 hours, almost the entire dose has been cleared from the intestine. Transit times in mice with stomach and intestines containing food were 12 hours longer than in fasted mice. These results lead to the conclusion that factors other than G.I. residence time determine G.I. absorption of actinides in mice

  5. Process optimization for effective column separation of 106Ru from aqueous waste associated with spent reprocessing solvent in storage tanks

    The present work deals with another waste stream resulting from reprocessing operations, viz. the aqueous solution present in substantial quantities as the bottom layer in tanks storing spent TBP-dodecane solvent. The effective separation of 106Ru from aqueous waste streams generated during reprocessing of spent nuclear fuel is difficult because of its complex aqueous chemistry

  6. Kinetic study of the deposition of 144Ce, 143Pr and 147Nd on a platinum anode

    Investigation of the electrodeposition of radioactive rare earth metal isotopes confirm that, depending on the conditions of electrolysis, they can be deposited on the platinum either cathodically or anodically. The anodic deposition of these isotopes can take place with electrochemical oxidation or electrosorption without electron-transfer, depending on the lanthanide(III-IV) oxidation potentials. The present paper reports the results of the investigation connected with the anodic deposition of 144Ce, 143Pr and 147Nd. (author)

  7. Biological effects of repeated inhalation exposure of Beagle dogs to relatively insoluble aerosols of 144Ce. VI

    Beagle dogs were exposed repeatedly to a relatively insoluble form of 144Ce (in fused aluminosilicate particles) to study the deposition, retention and long-term biological effects for comparison with data from dogs that were exposed only once to a similar aerosol. Four groups of nine dogs each were exposed once every 8 weeks for 2 years (13 exposures) to achieve specified exposure goals. These goals were: to increase the lung burden by 2.5 μCi 144Ce/kg body weight with each exposure; to reestablish lung burdens of 9 or 4.5 μCi 144Ce/kg body weight and to expose controls to fused aluminosilicate particles containing nonradioactive cerium. With these exposure sequences, the 144Ce-exposed dogs received increasing or relatively constant beta radiation dose rates in contrast to the steadily decreasing dose rate seen after a single inhalation exposure. Following completion of the exposure series, the dogs are being observed for the development of long-term biological effects. To date, 11 dogs have died or were euthanized, nine exposed dogs and two controls. Although pulmonary hemangiosarcomas were a prominent finding in dogs exposed once to the same aerosol at a level that led to cumulative doses to lung similar to these repeatedly exposed dogs, only one has been observed in the repeatedly exposed dogs. Other effects of note to date include three pulmonary carcinomas, two hemangiosarcomas of the tracheobronchial lymph nodes and one splenic hemangiosarcoma. Observations are continuing on the surviving 18 exposed and seven control dogs

  8. 129I, 60Co, and 106Ru measurements on water samples from the Hanford project environs

    Groundwater flow and contamination patterns beneath the Hanford project reservation have been studied since the early days of the project. The measurement of radioactive materials at concentrations much below those required for radiation protection are useful for tracing groundwater movement and detection of potential contamination problems before they are apt to occur. Groundwater samples from a number of wells on or near the Hanford reservation have been analyzed for 129I by neutron activation analysis and for gamma radioactivity by low-level coincidence gamma-ray spectrometry. The major radionuclides in addition to natural radioactivity detected in the underground waters by gamma-ray spectrometry were 106Ru and 60Co. Local river and rain water samples were also analyzed for 129I and long-lived radionuclides. Special sample collection methods were developed to prevent contamination of the water samples during collection. Anions travel farther than cations in underground water systems since soils are primarily cation exchangers and retain the cations. Anion exchange techniques were used in the field and the laboratory to recover the desired radionuclides. Sample sizes ranged up to several thousand liters. This paper discusses the sample collection methods,analysis methods, and results obtained. The methods used were found to provide high sensitivity for groundwater studies. (auth)

  9. Use of 141Ce as a particulate digesta flow tracer in ruminants. II. Behavior of the tracer at the duodenum and in the feces

    A ration of 600 g chopped hay and 150 g ground sorghum is given twice daily to sheep fitted with a rumen cannula and a duodenal reentrant cannula. 141Ce flow rate at the duodenum and in the feces is compared to flow rate of stained hay particles after ingestion of a single labelled meal. After an adaptation period during which both daily meals are labelled, variations in 141Ce concentration are then measured in the duodenal and fecal dry matter. The tracer is used to estimate dry mater digestibility indirectly. Duodenal data show that the mean retention time of 141Ce in the rumen is about 15% less than that of stained particles. The meal after the radioactive one momentarily depresses 141Ce excretion rate while it accelerates that of the stained particles. Mean retention time in the whole gastro-intestinal tract of a meal of 600 g chopped hay 150 g ground sorghum is 40.4+-3.8 h or 32.4+-3.7 h, depending on whether stained particles or 141Ce is used. All the 141Ce ingested is recovered in the feces. Mean recovery of 141Ce in the feces excreted during 200 hours after dosage is 100.2+-5.0%. After a period of adaptation where all meals are radioactive, feces of 2 sheep are sampled either by total collection or directly in the rectum. Dry matter digestibility does not differ whether calculated from total collection or by the indirect method using 141Ce

  10. Decontamination of 60Co and 144Ce. low-activity liquid wastes with the Fe3+ /OH- /Ca2+ /PO-4-3- system

    The influence of reaction time, concentrations of Fe3+ and PO-4-3+, temperature and agitation velocity in the efficiency of decontamination of 60Co and 144Ce low-activity liquid wastes using the Fe3+ /OH-/Ca2+ /PO-4-3+ precipitator system was stud ied in this paper. The mathematical models of this process were obtained for 60Co and 144Ce. The best conditions for the decontamination we re calculated using the optimization program

  11. Studies on the chemical behaviour of 106Ru in sea water and its uptake by marine organisms

    In the previous paper, the author represented that the concentration factor of 106Ru was relatively high for marine algae in comparison with the other organisms such as fish and mollusca. The concentration seemed to be attributable to the effect of adsorption on the surface of the marine algae. And it is well known that the surface substance is quite different according to the species of marine algae. Then uptake behaviour of the ionic species obtained from 106RuNO.Cl sub(x) were investigated in relation to the species of marine algae and the surface substances extracted from them. The cationic complex species represented the highest concentration factors for the two species except red algae. The order of the concentration factors among these was as follows: brown algae (Hizikia fusiforme) > green algae (Ulva pertusa) > red algae (Porphyra tenera). (auth.)

  12. Assessment of ocular beta radiation dose distribution due to 106Ru/106Rh brachytherapy applicators using MCNPX Monte Carlo code

    Nilseia Aparecida Barbosa

    2014-08-01

    Full Text Available Purpose: Melanoma at the choroid region is the most common primary cancer that affects the eye in adult patients. Concave ophthalmic applicators with 106Ru/106Rh beta sources are the more used for treatment of these eye lesions, mainly lesions with small and medium dimensions. The available treatment planning system for 106Ru applicators is based on dose distributions on a homogeneous water sphere eye model, resulting in a lack of data in the literature of dose distributions in the eye radiosensitive structures, information that may be crucial to improve the treatment planning process, aiming the maintenance of visual acuity. Methods: The Monte Carlo code MCNPX was used to calculate the dose distribution in a complete mathematical model of the human eye containing a choroid melanoma; considering the eye actual dimensions and its various component structures, due to an ophthalmic brachytherapy treatment, using 106Ru/106Rh beta-ray sources. Two possibilities were analyzed; a simple water eye and a heterogeneous eye considering all its structures. Two concave applicators, CCA and CCB manufactured by BEBIG and a complete mathematical model of the human eye were modeled using the MCNPX code. Results and Conclusion: For both eye models, namely water model and heterogeneous model, mean dose values simulated for the same eye regions are, in general, very similar, excepting for regions very distant from the applicator, where mean dose values are very low, uncertainties are higher and relative differences may reach 20.4%. For the tumor base and the eye structures closest to the applicator, such as sclera, choroid and retina, the maximum difference observed was 4%, presenting the heterogeneous model higher mean dose values. For the other eye regions, the higher doses were obtained when the homogeneous water eye model is taken into consideration. Mean dose distributions determined for the homogeneous water eye model are similar to those obtained for the

  13. Biological alterations resulting from chronic lung irradiation. I. The pulmonary lipid composition, physiology, and pathology after inhalation by beagle dogs of 144Ce-labeled fused clay aerosols

    Three groups of four beagle dogs inhaled a 144Ce-labeled fused clay aerosol; two additional dogs per group, exposed to a stable cerium-labeled fused clay aerosol, were used as controls. At monthly intervals, one diaphragmatic lobe of each of two dogs exposed to 144Ce and one control animal from each group was lavaged with isotonic saline. The recovered lavage solutions were centrifuged to isolate lung cells (mostly macrophages) and surfactant for lipid analyses. The groups were sacrificed at 2, 4, and 6 mo after exposure, when the lungs of the dogs exposed to 144Ce had average cumulative radiation doses of 23, 36, and 59 krad, respectively. Chronic irradiation of the lung resulted in a progressive radiation pneumonitis which was assessed clinically and pathologically at various intervals. At sacrifice, the lungs were analyzed for 144Ce and the right apical and diaphragmatic lobes were minced and lyophilized and the lipids were extracted. Total lipids from all lung samples were determined gravimetrically and individual compounds were identified, isolated, and quantitated. The quantities of lipid in lung tissue, in pulmonary cells, and in surfactant increased as a function of time and radiation dose. Neutral lipids (sterol esters and triglycerides) accounted for most of the increase. (U.S.)

  14. Responses of different dosemeters in beta dosimetry of {sup 106}Ru/{sup 106}Rh ophthalmic applicators;Respostas de diferentes dosimetros termoluminescentes na dosimetria beta de aplicadores oftalmicos de {sup 106}Ru/{sup 106}Rh

    Ferreira, D.F.P.; Daros, K.A.C.; Segreto, R.A.; Medeiros, R.B. [Universidade Federal de Sao Paulo (UNIFESP), Sao Paulo, SP (Brazil)

    2009-07-01

    This work presents the TL response of three kinds of dosimeters from different manufacturing characteristics under irradiation of 106 Ru / 106 Rh sealed sources used in ophthalmic brachytherapy. They are: Ca SO{sub 4}:Dy + teflon (D- Ca SO{sub 4}:Dy -0,4), LiF:Mg, Ti (TLD-100) and Ca SO{sub 4}:Dy (TLD-900). Some of reports accepted by scientific community (NCS report 14 e ICRU report 72) as reference in the quality control of beta applicators dosimetry recommend that the absorbed dose standard uncertainties can be kept below 20%. The TLD Ca SO{sub 4}:Dy + teflon presented proper sensibility and high precision comparing with the others. Considering the similar dimensions of ophthalmic tumors and aside critical structures it is relevant to reduce undesirable effects due to the irradiation of these structures. Therefore, the quality control in the beta dosimetry using this kind of source is a constant challenge. (author)

  15. Assessment, modelization and analysis of {sup 106} Ru experimental transfers through a freshwater trophic system; Evaluation, modelisation et analyse des transferts experimentaux du {sup 106}Ru au sein d`un reseau trophique d`eau douce

    Vray, F.

    1994-11-24

    Experiments are carried out in order to study {sup 106} RU transfers through a freshwater ecosystem including 2 abiotic compartments (water and sediment) and 3 trophic levels (10 species). Experimental results are expressed mathematically so as they can be included into a global model which is then tested in two different situations. The comparison of the available data concerning the in situ measured concentrations to the corresponding calculated ones validates the whole procedure. Analysis of the so validated results lightens ruthenium distribution process in the environment. The rare detection of this radionuclide in organisms living in areas contaminated by known meaningful releases can be explained by a relativity high detection limit and by a slight role of the sediment as a secondary contamination source. (author). 78 figs., 18 tabs.

  16. Process for the removal of 106Ru traces from NH4NO3 effluent generated during recycling of sintered depleted uranium fuel pellets

    Several chemical treatment formulations were tested for the effective removal of very low levels of 106Ru activity from NH4NO3 effluent generated during wet processing of rejected sintered depleted uranium (DU) fuel pellets. Based on the results, a simple process involving precipitation of cobalt sulphide along with ferric hydroxide was selected and further optimization of process variables was carried out. The optimized process has been found to be highly efficient in reducing 106Ru activity down to extremely low levels. (author)

  17. Energy deposition by a 106Ru/106Rh eye applicator simulated using LEPTS, a low-energy particle track simulation

    The present study introduces LEPTS, an event-by-event Monte Carlo programme, for simulating an ophthalmic 106Ru/106Rh applicator relevant in brachytherapy of ocular tumours. The distinctive characteristics of this code are the underlying radiation-matter interaction models that distinguish elastic and several kinds of inelastic collisions, as well as the use of mostly experimental input data. Special emphasis is placed on the treatment of low-energy electrons for generally being responsible for the deposition of a large portion of the total energy imparted to matter. - Highlights: → We present the Monte Carlo code LEPTS, a low-energy particle track simulation. → Carefully selected input data from 10 keV to 1 eV. → Application to an electron emitting Ru-106/Rh-106 plaque used in brachytherapy.

  18. Separation and purification of 106Ru from effluent streams of ion exchange cycle used for Pu purification in PUREX process

    Present paper describes the separation and purification of extracted fraction of Ru using separation techniques namely solvent extraction and extraction chromatography. The feed solution used is ion exchange effluent solution collected from Plant that contained 106Ru activity of ∼ 100 mCi/L level along with 95Nb (∼ 0.29 mCi/L) and Pu (∼ 1.5mg/L) at 7.1 M HNO3. In the initial step, the feed solution is contacted ice with 30% TBP in n-dodecane at organic to aqueous phase ratio of 2:1. The raffinate from this step shows that the free acidity of the solution is reduced from 7.1 to 4.2 M without loosing the Ru activity in the feed

  19. Multidimensional dosimetry of {sup 106}Ru eye plaques using EBT3 films and its impact on treatment planning

    Heilemann, G., E-mail: gerd.heilemann@meduniwien.ac.at; Kostiukhina, N. [Department of Radiation Oncology/Comprehensive Cancer Center, Medical University of Vienna/AKH Vienna, Vienna 1090 (Austria); Nesvacil, N.; Georg, D. [Department of Radiation Oncology/Comprehensive Cancer Center, Medical University of Vienna/AKH Vienna, Vienna 1090, Austria and Christian Doppler Laboratory for Medical Radiation Research for Radiation Oncology, Vienna 1090 (Austria); Blaickner, M. [Health and Environment Department Biomedical Systems, Austrian Institute of Technology GmbH, Vienna 1220 (Austria)

    2015-10-15

    Purpose: The purpose of this study was to establish a method to perform multidimensional radiochromic film measurements of {sup 106}Ru plaques and to benchmark the resulting dose distributions against Monte Carlo simulations (MC), microdiamond, and diode measurements. Methods: Absolute dose rates and relative dose distributions in multiple planes were determined for three different plaque models (CCB, CCA, and COB), and three different plaques per model, using EBT3 films in an in-house developed polystyrene phantom and the MCNP6 MC code. Dose difference maps were generated to analyze interplaque variations for a specific type, and for comparing measurements against MC simulations. Furthermore, dose distributions were validated against values specified by the manufacturer (BEBIG) and microdiamond and diode measurements in a water scanning phantom. Radial profiles were assessed and used to estimate dosimetric margins for a given combination of representative tumor geometry and plaque size. Results: Absolute dose rates at a reference depth of 2 mm on the central axis of the plaque show an agreement better than 5% (10%) when comparing film measurements (MCNP6) to the manufacturer’s data. The reproducibility of depth-dose profile measurements was <7% (2 SD) for all investigated detectors and plaque types. Dose difference maps revealed minor interplaque deviations for a specific plaque type due to inhomogeneities of the active layer. The evaluation of dosimetric margins showed that for a majority of the investigated cases, the tumor was not completely covered by the 100% isodose prescribed to the tumor apex if the difference between geometrical plaque size and tumor base ≤4 mm. Conclusions: EBT3 film dosimetry in an in-house developed phantom was successfully used to characterize the dosimetric properties of different {sup 106}Ru plaque models. The film measurements were validated against MC calculations and other experimental methods and showed a good agreement with

  20. Suppression of the pulmonary clearance of Staphylococcus aureus in mice that had inhaled either 144CeO2 or 239PuO2

    The rate of pulmonary clearance of inhaled Staphylococcus aureus in mice was determined at intervals after inhalation exposure to either 144CeO2 or 239PuO2. In mice with mean initial lung burdens between 0.6 and 4.7 μCi 144Ce the pulmonary clearance of S. aureus was suppressed up to 12 weeks after inhalation of 144CeO2. In mice with mean initial lung burdens between 1.3 and 29.0 μCi 239Pu the pulmonary clearance of S. aureus was suppressed up to 26 weeks after inhalation of 239PuO2. The suppressed pulmonary clearance of S. aureus appeared to correlate with the radiation dose rate to the lungs at the time of exposure to bacteria but not with the cumulative radiation dose to the lungs. The changes in bacterial clearance did not appear to be correlated with changes in body weight, hematological parameters, or radiation-induced histopathological changes. Altered bacterial clearance may be related to radiation damage to pulmonary macrophages. It was concluded that irradiation of the lung from radionuclides inhaled in relatively insoluble forms may result in increased bacterial invasion of the lungs

  1. Use of 141Ce as a particulate digesta flow tracer in ruminants. I. Determination of uptake on feed and behavior in rumen digesta in vivo

    The suitability of 141Ce as a particulate digesta flow tracer is studied in sheep. The amount and the factors of cerium uptake on feed particles by incubating alfalfa hay and sorghum seeds in water containing 141Ce in solution are determined. After soaking one hour, 80% radioactivity is retained on the hay 17% on the sorghum. Incubation time is the main factor determining uptake rate. This uptake is solid on the hay and more fragile on the sorghum. The evolution of 141Ce distribution among the different physical constituents of rumen digesta is studied on two sheep given a single radioactive meal (10μCi). These sheep are fitted with a rumen cannula and fed twice daily with hay (80%) and sorghum (20%). There is little 141Ce in solution in the supernatant liquid after centrifugation of digesta. At the end of the 'labelled' meal, specific radioactivity (RAS) of liquid-phase digesta, separated by filtering on two layers of gauze, is equal to or higher than the RAS of the solid phase. It increases up to the next unlabelled meal and then decreases. Microorganisms may cause this transfer of liquid-phase radioactivity to the large particles. Specific radioactivity of the microorganisms remains very high after the 'labelled' meal as compared to that of different granulometric fractions of solid digesta

  2. Determination of 106Ru, 134/137Cs, and 241Am concentrations and Action Level in the Foodstuffs Consumed by Inhabitants of Iraq

    *H. N. Majeed

    2013-03-01

    Full Text Available The specific activity concentrations of (106Ru, 134/137Cs, and 241Am nuclides in 40 imported foodstuffs which collected randomly in January 2012 from all Iraqi cities markets were studied. The rang of specific activity concentrations of 106Ru varies from (37.930±6.16 Bq kg-1 (S No. :17: Turkey Kidney bean to 99.735±9.99 Bq kg-1 (S No.:32: Egypt Broad bean, with average value 71.667±8.47 Bq kg-1. For 134Cs varies from 0.200±0.45 Bq kg-1 (S No. :19 : Ukraine Chick-pea to 2.365±1.54 Bq kg-1 (S No. :33 : Peru Broad bean with average value (0.988±0.99 Bq kg-1.The activity concentrations of 137Cs varies from 0.164±0.40 Bq kg-1 (S No.:19 : Ukraine Chick-pea to 5.291±2.30 Bq kg-1 ( S No.: 39: Uzbekistan Mung bean with average value 1.460±1.21, then for 241Am the activity concentrations varies from 0.029±0.17 Bq kg-1 (S No.:23 : Iran Chick-pea to 1.248±1.12 Bq kg-1 (S No.:40: Canada Green peas with average value 0.399±0.63. All the values were less than the World average concentrations [15,17]. The high contributor for 106Ru, 134/137Cs, and 241Am radionuclides were in Broad bean and other foodstuffs (which contained Brown grit, White grit, Mung bean and Green peas as a 12%, Broad bean as 14%, corn as a 19% and other foodstuffs with 15% respectively The lowest contributor of 106Ru, 134/137Cs, and 241Am radionuclides in the studied foodstuffs were 6% in cowpea, 7% in semolina, 5% in lentil and 4% in lentil respectively. The action level of the 106Ru, 134/137Cs, and 241Am radionuclide’s for three age groups have been calculated and the foodstuffs were within the range permitted and free of any radiation and thus there was no seriousness in dealing with.

  3. Evolution of gamma artificial radioactivity in coastal sediments of the English Channel during the years 1976, 1977 and 1978

    During 1976-1977, a state of equilibrium was found to prevail for 106Ru and 144Ce, especially in the North-West Cotentin and the Norman-Breton gulf, where reconcentration of both radionuclides was observed with preferential enrichment of the latter over the former. Levels of 125Sb and 137Cs were found to be low but were difficult to interpret, because of the particular physico-chemical behavior of 125Sb and the long half-life of 137Cs. The results obtained for 103Ru, 141Ce, 95Zr may be explained entirely by the contribution of atmospheric fallout. 144Ce and 106Ru levels in the Norman-Breton gulf may be for the most part ascribed to La Hague disposals, radionuclide dispersal from the emissary being characterized by an eastward transfer of the soluble fraction and a westward transfer of the particulate fraction, with transit times which may last up to 2 years. The boundary between the areas submitted respectively to the twofold impact of fallout and industrial waste, and to fallout alone would appear to lie between the mouth of the Trieux river and Morlaix Bay. From a graphic representation of the relationship between radionuclides, empiric distribution laws for 106Ru and 137Cs were established from 144Ce level parameters characteristic of the areas considered (years 1976-1977)

  4. Nondestructive analysis of RA reactor fuel burnup, Program for burnup calculation base on relative yield of 106Ru, 134Cs and 137Cs in the irradiated fuel

    Burnup of low enriched metal uranium fuel of the RA reactor is described by two chain reactions. Energy balance and material changes in the fuel are described by systems of differential equations. Numerical integration of these equations is base on the the reactor operation data. Neutron flux and percent of Uranium-235 or more frequently yield of epithermal neutrons in the neutron flux, is determined by iteration from the measured contents of 106Ru, 134Cs and 137Cs in the irradiated fuel. The computer program was written in FORTRAN-IV. Burnup is calculated by using the measured activities of fission products. Burnup results are absolute values

  5. Quantitative analysis of fission products by γ spectrography

    The activity of the fission products present in treated solutions of irradiated fuels is given as a function of the time of cooling and of the irradiation time. The variation of the ratio (144Ce + 144Pr activity)/ 137Cs activity) as a function of these same parameters is also given. From these results a method is deduced giving the 'age' of the solution analyzed. By γ-scintillation spectrography it was possible to estimate the following elements individually: 141Ce, 144Ce + 144Pr, 103Ru, 106Ru + 106Rh, 137Cs, 95Zr + 95Nb. Yield curves are given for the case of a single emitter. Of the various existing methods, that of the least squares was used for the quantitative analysis of the afore-mentioned fission products. The accuracy attained varies from 3 to 10%. (author)

  6. Energy deposition by a {sup 106}Ru/{sup 106}Rh eye applicator simulated using LEPTS, a low-energy particle track simulation

    Fuss, M.C. [Instituto de Fisica Fundamental, Consejo Superior de Investigaciones Cientificas (CSIC), Serrano 113-bis, 28006 Madrid (Spain); Munoz, A.; Oller, J.C. [Centro de Investigaciones Energeticas, Medioambientales y Tecnologicas (CIEMAT), Avenida Complutense 22, 28040 Madrid (Spain); Blanco, F. [Departamento de Fisica Atomica, Molecular y Nuclear, Universidad Complutense de Madrid, Avenida Complutense, 28040 Madrid (Spain); Williart, A. [Departamento de Fisica de los Materiales, Universidad Nacional de Educacion a Distancia, Senda del Rey 9, 28040 Madrid (Spain); Limao-Vieira, P. [Laboratorio de Colisoes Atomicas e Moleculares, Departamento de Fisica, CEFITEC, FCT-Universidade Nova de Lisboa, Quinta da Torre, 2829-516 Caparica (Portugal); Borge, M.J.G.; Tengblad, O. [Instituto de Estructura de la Materia, Consejo Superior de Investigaciones Cientificas (CSIC), Serrano 113-bis, 28006 Madrid (Spain); Huerga, C.; Tellez, M. [Hospital Universitario La Paz, Paseo de la Castellana 261, 28046 Madrid (Spain); Garcia, G., E-mail: g.garcia@iff.csic.es [Instituto de Fisica Fundamental, Consejo Superior de Investigaciones Cientificas (CSIC), Serrano 113-bis, 28006 Madrid (Spain); Departamento de Fisica de los Materiales, Universidad Nacional de Educacion a Distancia, Senda del Rey 9, 28040 Madrid (Spain)

    2011-09-15

    The present study introduces LEPTS, an event-by-event Monte Carlo programme, for simulating an ophthalmic {sup 106}Ru/{sup 106}Rh applicator relevant in brachytherapy of ocular tumours. The distinctive characteristics of this code are the underlying radiation-matter interaction models that distinguish elastic and several kinds of inelastic collisions, as well as the use of mostly experimental input data. Special emphasis is placed on the treatment of low-energy electrons for generally being responsible for the deposition of a large portion of the total energy imparted to matter. - Highlights: > We present the Monte Carlo code LEPTS, a low-energy particle track simulation. > Carefully selected input data from 10 keV to 1 eV. > Application to an electron emitting Ru-106/Rh-106 plaque used in brachytherapy.

  7. CeLAND: search for a 4th light neutrino state with a 3 PBq 144Ce-144Pr electron antineutrino generator in KamLAND

    Gando, A; Hayashida, S; Ikeda, H; Inoue, K; Ishidoshiro, K; Ishikawa, H; Koga, M; Matsuda, R; Matsuda, S; Mitsui, T; Motoki, D; Nakamura, K; Oki, Y; Otani, M; Shimizu, I; Shirai, J; Suekane, F; Suzuki, A; Takemoto, Y; Tamae, K; Ueshima, K; Watanabe, H; Xu, B D; Yamada, S; Yamauchi, Y; Yoshida, H; Cribier, M; Durero, M; Fischer, V; Gaffiot, J; Jonqueres, N; Kouchner, A; Lasserre, T; Leterme, D; Letourneau, A; Lhuillier, D; Mention, G; Rampal, G; Scola, L; Veyssiere, Ch; Vivier, M; Yala, P; Berger, B E; Kozlov, A; Banks, T; Dwyer, D; Fujikawa, B K; Han, K; Kolomensky, Yu G; Mei, Y; O'Donnell, T; Decowski, P; Markoff, D M; Yoshida, S; Kornoukhov, V N; Gelis, T V M; Tikhomirov, G V; Learned, J G; Maricic, J; Matsuno, S; Milincic, R; Karwowski, H J; Efremenko, Y; Detwiler, A; Enomoto, S

    2013-01-01

    The reactor neutrino and gallium anomalies can be tested with a 3-4 PBq (75-100 kCi scale) 144Ce-144Pr antineutrino beta-source deployed at the center or next to a large low-background liquid scintillator detector. The antineutrino generator will be produced by the Russian reprocessing plant PA Mayak as early as 2014, transported to Japan, and deployed in the Kamioka Liquid Scintillator Anti-Neutrino Detector (KamLAND) as early as 2015. KamLAND's 13 m diameter target volume provides a suitable environment to measure the energy and position dependence of the detected neutrino flux. A characteristic oscillation pattern would be visible for a baseline of about 10 m or less, providing a very clean signal of neutrino disappearance into a yet-unknown, sterile neutrino state. This will provide a comprehensive test of the electron dissaperance neutrino anomalies and could lead to the discovery of a 4th neutrino state for Delta_m^2 > 0.1 eV^2 and sin^2(2theta) > 0.05.

  8. A Brief Review of Past INL Work Assessing Radionuclide Content in TMI-2 Melted Fuel Debris: The Use of 144Ce as a Surrogate for Pu Accountancy

    D. L. Chichester; S. J. Thompson

    2013-09-01

    This report serves as a literature review of prior work performed at Idaho National Laboratory, and its predecessor organizations Idaho National Engineering Laboratory (INEL) and Idaho National Engineering and Environmental Laboratory (INEEL), studying radionuclide partitioning within the melted fuel debris of the reactor of the Three Mile Island 2 (TMI-2) nuclear power plant. The purpose of this review is to document prior published work that provides supporting evidence of the utility of using 144Ce as a surrogate for plutonium within melted fuel debris. When the TMI-2 accident occurred no quantitative nondestructive analysis (NDA) techniques existed that could assay plutonium in the unconventional wastes from the reactor. However, unpublished work performed at INL by D. W. Akers in the late 1980s through the 1990s demonstrated that passive gamma-ray spectrometry of 144Ce could potentially be used to develop a semi-quantitative correlation for estimating plutonium content in these materials. The fate and transport of radioisotopes in fuel from different regions of the core, including uranium, fission products, and actinides, appear to be well characterized based on the maximum temperature reached by fuel in different parts of the core and the melting point, boiling point, and volatility of those radioisotopes. Also, the chemical interactions between fuel, fuel cladding, control elements, and core structural components appears to have played a large role in determining when and how fuel relocation occurred in the core; perhaps the most important of these reaction appears to be related to the formation of mixed-material alloys, eutectics, in the fuel cladding. Because of its high melting point, low volatility, and similar chemical behavior to plutonium, the element cerium appears to have behaved similarly to plutonium during the evolution of the TMI-2 accident. Anecdotal evidence extrapolated from open-source literature strengthens this logical feasibility for

  9. The study of the effect of gamma radiation on the ionic and collodial solutions of 144Ce/III/ at trace concentration by the method of self-diffusion and centrifugation

    Gamma irradiation of a solution of trace concentration of 144Ce/III/ at pH 3.0 causes an increase in the self-diffusion coefficient of 144Ce/III/ and small decrease in its centrifugable fraction. The significant increase in the self-diffusion coefficient is observed after irradiation at pH 9.0 and 11.0 and on the centrifugation of these solutions an increased susceptibility of particles containing 144Ce/III/ to the coagulation accurs. The measurements were performed by a method of the open end capillary immersed into the excess of inactive solution and the self-diffusion coefficient calculated as described earlier. The solutions were irradiated either directly in the capillaries for the self-diffusion measurment fixed in the glass tubes or in borosilicate Sial glass sample tubes with subsequent pipetting into the capillaries. The dose rate of 60Co γ-radiation was about 0.4 Mrad. hour-1, the time of irradiation was 1.5 to 15 hours. The period between the end of the irradiation and the beginning of the self-diffusion measurement amounted to about 15 to 30 min. (F.G.)

  10. Does escalation of the apical dose change treatment outcome in β-radiation of posterior choroidal melanomas with 106Ru plaques?

    Purpose: To show the results of treating posterior uveal melanomas with 106Ru plaque β-ray radiotherapy and to review and discuss the literature concerning the optimal apical dose prescription (100 vs. 160 Gy). Methods and Materials: Forty-eight patients with uveal melanomas (median height 3.85 mm + 1 mm sclera) were treated with ruthenium plaques. The median apical dose was 120 Gy, the median scleral dose 546 Gy. Results: After 5.8 years of follow-up, the overall 5-year survival rate was 90%, the disease specific 5-year survival rate was 92% (3 patients alive with metastasis). Six percent received a second ruthenium application, 10% of the eyes had to be enucleated. Local control was achieved in 90% of the patients with conservative therapy alone. Central or paracentral tumors showed 50% of the pretherapeutic vision after 4 years, and 80% of the vision was preserved in those with peripheral tumors. The main side effects were mostly an uncomplicated retinopathy (30%); macular degeneration or scarring led to poor central vision in 30% of cases. Conclusion: Brachytherapy with ruthenium applicators is an effective therapy for small- and medium-size posterior uveal melanomas. Our results are comparable to other series. The treatment outcome does not seem to be capable of improvement by increasing the apical dose. An internationally accepted model for defining the dosage in brachytherapy is needed

  11. Studies on treatment of low level radioactive liquid waste for removal of anionic species of 125Sb, 99Tc and 106Ru. Contributed Paper RD-14

    The treatment of intermediate level waste at Waste Immobilization Plant generates low level radioactive waste which would require further management before discharge to sea. This waste is expected to contain polymeric oxo anions of 125Sb, 99Tc, 106Ru in addition to cationic species like 137Cs, 90Sr etc. Chemical treatment takes care of the major contributors to radioactivity viz 137Cs, 90Sr etc but traces of activity due to anionic species remain in the treated waste effluent. Novel composite anionic exchanger namely Polyurethane foam coated with Hydrous Zirconium Oxide was developed for removal of these anionic species. This material was successfully employed for removal of anionic 125Sb from radioactive waste effluent at Waste Management Division, Trombay. Based on our experience with Sb removal using the above material it was decided to assess the ability of the exchanger in removal of other anionic species bearing Ru and Tc. It was observed that in addition to complete removal of Sb, 50% Ru removal and 40% Tc could also be removed using this material from radioactive waste effluents. In lab experiments, similar results were obtained with simulated low level waste bearing inactive Ru. Among several hydrous oxides tried in a batch study, Hydrous Zirconium Oxide showed a maximum removal of 40% for Tc in actual waste generated from reprocessing plant. Based on the above it has been planned to set up an anion exchange column with Hydrous Zirconium Oxide coated Polyurethane foam for final treatment of chemically treated waste effluent prior to discharge as a prime step towards achieving our goal of minimum discharge to Sea. (author)

  12. Radiochemical methods used by the IAEA's laboratories at Siebersdorf for the determination of 90Sr, 144Ce and Pu radionuclides in environmental samples collected for the International Chernobyl Project

    During the IAEA's International Chernobyl Project to assess the radiological consequences of the nuclear reactor accident, the Agency's Laboratories at Seibersdorf participated in the collection and analyses of environmental samples from the Soviet Union. Under Task 2 of this effort, the determination of the activity concentrations of 90Sr and the alpha-emitting Pu radionuclides was important for the corroboration of the official USSR environmental contamination maps. The present paper describes in detail the sampling methods and radiochemical procedures used for the 90Sr, 144Ce, 238Pu and 239,240Pu analyses in these samples with emphasis on the grass and soil treatments. (Author)

  13. Determination of absorbed dose distribution in water for COC ophthalmic applicator of {sup 106}Ru/{sup 106}Rh using Monte Carlo code-MCNPX; Determinacao da distribuicao de dose absorvida na agua para o aplicador oftalmico COC de {sup 106}Ru/{sup 106}Rh utilizando o codigo de Monte Carlo - MCNPX

    Barbosa, Nilseia A.; Rosa, Luiz A. Ribeiro da, E-mail: nilseia@ird.gov.br, E-mail: lrosa@ird.gov.br [Instituto de Radioprotecao e Dosimetria (IRD/CNEN-RJ),Rio de Janeiro, RJ (Brazil); Braz, Delson, E-mail: delson@nuclear.ufrj.br [Coordenacao dos programas de Pos-Graduacao em Engenharia (PEN/COPPE/UFRJ), Rio de Janeiro, RJ (Brazil). Programa de Engenharia Nuclear

    2014-07-01

    The COC ophthalmic applicators using beta radiation source of {sup 106}Ru/{sup 106}Rh are used in the treatment of intraocular tumors near the optic nerve. In this type of treatment is very important to know the dose distribution in order to provide the best possible delivery of prescribed dose to the tumor, preserves the optic nerve region extremely critical, that if damaged, can compromise the patient's visual acuity, and cause brain sequelae. These dose distributions are complex and doctors, who will have the responsibility on the therapy, only have the source calibration certificate provided by the manufacturer Eckert and Ziegler BEBIG GmbH. These certificates provide 10 absorbed dose values at water depth along the central axis applicator with the uncertainties of the order of 20% isodose and in a plane located 1 mm from the applicator surface. Thus, it is important to know with more detail and precision the dose distributions in water generated by such applicators. To this end, the Monte Carlo simulation was used using MCNPX code. Initially, was validated the simulation by comparing the obtained results to the central axis of the applicator with those provided by the certificate. The different percentages were lower than 5%, validating the used method. Lateral dose profile was calculated for 6 different depths in intervals of 1 mm and the dose rates in mGy.min{sup -1} for the same depths.

  14. Assessment of selected fission products in the Savannah River Site environment

    Most of the radioactivity produced by the operation of a nuclear reactor results from the fission process, during which the nucleus of a fissionable atom (such as 235U) splits into two or more nuclei, which typically are radioactive. The Radionuclide Assessment Program (RAP) has reported on fission products cesium, strontium, iodine, and technetium. Many other radionuclides are produced by the fission process. Releases of several additional fission products that result in dose to the offsite population are discussed in this publication. They are 95Zr, 95Nb, 103Ru, 106Ru, 141Ce, and 144Ce. This document will discuss the production, release, migration, and dose to humans for each of these selected fission products

  15. Appendix to Health and Safety Laboratory environmental quarterly, March 1, 1976--June 1, 1976. [Tabulated data on content of lead in surface air and /sup 7/Be, /sup 95/Zr, /sup 137/Cs, /sup 144/Ce, and /sup 90/Sr in surface air, milk, drinking water, and foods sampled in USA

    Hardy, E.P. Jr.

    1976-07-01

    Tabulated data are presented on: the monthly deposition of /sup 89/Sr and /sup 90/Sr at some 100 world land sites; the content of lead and /sup 7/Be, /sup 95/Zr, /sup 137/Cs, and /sup 144/Ce in samples of surface air from various world sites; and the content of /sup 90/Sr in samples of milk, drinking water, and animal and human diets collected at various locations throughout the USA. (CH)

  16. Reconstruction of the composition of the Chernobyl radionuclide fallout and external radiation absorbed doses to the population in areas of Russia

    The results of reconstruction of the radionuclide composition of the Chernobyl fallout in the territories of Russia is presented. Reconstruction has been carried out by means of statistical analysis of the gamma spectrometry data on 2867 soil samples collected in the territories of Ukraine, Byelarus and Russia from 1986 to 1988. To verify the data, aggregated estimates of the fuel composition of the 4th block at the moment of the accident (available from the literature) have been used, as well as the estimates of activity released to the atmosphere. As a result, correlation and regression dependences have been obtained between the activities of the radionuclides most contributing to the dose (137Cs, 134Cs, 131I, 140Ba, 140La, 95Zr, 95Nb, 103Ru, 106Ru, 141Ce, 144Ce, 125Sb). Statistically significant regression relations between different pairs of radionuclides (including analysis of the 'noise' contribution to the data) depending on the distance between the point of sample collection and the power station are presented for the 'north-east track' - the northern part of the 30 km zone and southern part of the Gomel 'district (Byelarus) and the Briansk, Kaluga, Tula and Orel districts (Russia). A methodology is also described for reconstructing space-time characteristics of the contamination of the territories by major dose-forming radionuclides released from the Chernobyl NPP 4th unit. (Author)

  17. Radioactivity in surface air and precipitation in Japan after the Chernobyl accident

    Radioactive plumes from the Chernobyl reactor accident first passed over Japan on 3 May 1986. Measurements of 103Ru, 131I and 137Cs in rainfall and airborne dust collected at Chiba near Tokyo show that, in fact, at least two or more kinds of plume arrived during May. Their altitudes were calculated to be about 1500 m in early May and 6300 m in late May. Radionuclides detected in 33 precipitation samples collected by the network of radiation monitoring stations from 1 to 22 May were 7Be, 89Sr, 90Sr, 95Zr, 95Nb, 103Ru, 106Ru, sup(110m)Ag, 125Sb, sup(129m)Te, 131I, 132Te, 132I, 134Cs, 136Cs, 137Cs, 140Ba, 140La, 141Ce and 144Ce. The radiation was characterized by higher levels of the volatile nuclides, such as 103Ru, 132Te, 131I and 137Cs, than fallout levels in nuclear weapons testing, and by activity ratios of 0.48 and 14 for, respectively, 134Cs/137Cs and 89Sr/90Sr, as on 26 April. the fallout activity was higher in Northwestern Japan, the average depositions of 90Sr and 137Cs in Japan from 1 May (or 30 April) to 22 May being 1.4 Bq m-2 and 95 Bq m-2, inventories which are 14 and 550 times higher than the pre-Chernobyl values. (author)

  18. Biological effects of radiation: The induction of malignant transformation and programmed cell death

    In the Chernobyl explosions and fire, powderized nuclear fuel was released from the reactor core, causing an unexpected fallout. X-ray analysis and scanning electron microscopy showed that the isolated single particles were essentially pure uranium. These uranium aerosols contained all of the nonvolatile fission products, including the b-emitters, 95Zr, 103Ru, 106Ru, 141Ce, and 144Ce. The hot particles are extremely effective in inducing malignant transformation in mouse fibroblast cells in vitro. The major factor responsible for this effect is focus promotion caused by a wound-mediated permanent increase in cell proliferation (mitogenesis associated with mutagenesis). Transformed foci were analysed for the activation of c-abl, c-erb-A, c-erb-B, c-fms, c-fos, c-myb, c-myc, c-Ha-ras, c-Ki-ras, c-sis, and c-raf oncogenes at the transcriptional level. The pattern of oncogene activation was found to vary from focus to focus. Long interspersed repeated DNA (L1 or LINE makes up a class of mobile genetic elements which can amplify in the cell genome by retroposition. This element is spontaneously transcriptionally activated at a critical population density and later amplified in rat chloroleukaemia cells. UV light and ionizing radiation induce this activation prematurely, and the activation is followed by programmed cell death (apoptosis) in a sequence of events identical to that seen in LIRn activation occurring spontaneously

  19. Standard test method for gamma energy emission from fission products in uranium hexafluoride and uranyl nitrate solution

    American Society for Testing and Materials. Philadelphia

    2005-01-01

    1.1 This test method covers the measurement of gamma energy emitted from fission products in uranium hexafluoride (UF6) and uranyl nitrate solution. It is intended to provide a method for demonstrating compliance with UF6 specifications C 787 and C 996 and uranyl nitrate specification C 788. 1.2 The lower limit of detection is 5000 MeV Bq/kg (MeV/kg per second) of uranium and is the square root of the sum of the squares of the individual reporting limits of the nuclides to be measured. The limit of detection was determined on a pure, aged natural uranium (ANU) solution. The value is dependent upon detector efficiency and background. 1.3 The nuclides to be measured are106Ru/ 106Rh, 103Ru,137Cs, 144Ce, 144Pr, 141Ce, 95Zr, 95Nb, and 125Sb. Other gamma energy-emitting fission nuclides present in the spectrum at detectable levels should be identified and quantified as required by the data quality objectives. 1.4 This standard does not purport to address all of the safety concerns, if any, associated with its us...

  20. Monte Carlo modeling of beta-radiometer device used to measure milk contaminated as a result of the Chernobyl accident

    This paper presents results of Monte Carlo modeling of the beta-radiometer device with Geiger-Mueller detector used in Belarus and Russia to measure the radioactive contamination of milk after the Chernobyl accident. This type of detector, which is not energy selective, measured the total beta-activity of the radionuclide mix. A mathematical model of the beta-radiometer device, namely DP-100, was developed, and the calibration factors for the different radionuclides that might contribute to the milk contamination were calculated. The estimated calibration factors for 131I, 137Cs, 134Cs, 90Sr, 144Ce, and 106Ru reasonably agree with calibration factors determined experimentally. The calculated calibration factors for 132Te, 132I, 133I, 136Cs, 89Sr, 103Ru, 140Ba, 140La, and 141Ce had not been previously determined experimentally. The obtained results allow to derive the activity of specific radionuclides, in particular 131I, from the results of the total beta-activity measurements in milk. Results of this study are important for the purposes of retrospective dosimetry that uses measurements of radioactivity in environmental samples performed with beta-radiometer devices.

  1. Radionuclide accumulation by aquatic biota exposed to contaminated water in artificial ecosystems before and after its passage through the ground

    This study was designed to investigate the comparative accumulation of radionuclides from contaminated water in artificial ecosystems before and after the water's passage through the ground. Fish, clams, algae, and an emergent vascular plant were experimentally exposed to mixtures of radionuclides in three aqueous streams. Two streams consisted of industrial water discharged directly into a leaching trench, and the same water after it had migrated through the ground for a distance of 260 meters. The third stream was river water, which served as a background or control. Biota exposed to river water in the control stream had very low concentrations of 60Co, less than 3 pCi per gram dry weight (pCi/g DW). Other radionuclides were essentially unmeasurable. Biota exposed to trench water accumulated very high relative concentrations of 60Co. Biota exposed to trench water also had measurable concentrations of 155Eu, 144Ce, 141Ce, 125Sb, 124Sb, 103Ru, 106Ru, 137Cs, 95Zr, 95Nb, 58Co, 54Mn, 59Fe, 65Zn, 90Sr, /sup 239,240/Pu, and 238Pu. Biota exposed to ground water had concentrations of 60Co that ranged between 50 and 1200 pCi/g DW. Fish flesh had the lowest concentration of 60Co and algae the highest. Strontium-90 was measured in the tissues of aquatic biota at concentrations ranging between 360 pCi/g DW in clam flesh to 3400 pCi/g DW in leaves and stems of Veronica. Leaves and fruits of tomato plants rooted in the ground water accumulated 90Sr at concentrations of 160 pCi in fruits and 4200 pCi in leaves. Data indicate that 60Co and 90Sr migrated through the ground along with ground-water flow and were available to all classes of aquatic biota and tomato plants rooted in the water via root uptake, sorption, and food chain transfers. 8 refs., 4 figs., 6 tabs

  2. Particle size distribution of radioactive aerosols after the Fukushima and the Chernobyl accidents

    Following the Fukushima accident, a series of aerosol samples were taken between 24th March and 13th April 2011 by cascade impactors in the Czech Republic to obtain the size distribution of 131I, 134Cs, 137Cs, and 7Be aerosols. All distributions could be considered monomodal. The arithmetic means of the activity median aerodynamic diameters (AMADs) for artificial radionuclides and for 7Be were 0.43 and 0.41 μm with GDSs 3.6 and 3.0, respectively. The time course of the AMADs of 134Cs, 137Cs and 7Be in the sampled period showed a slight decrease at a significance level of 0.05, whereas the AMAD pertaining to 131I increased at a significance level of 0.1. Results obtained after the Fukushima accident were compared with results obtained after the Chernobyl accident. The radionuclides released during the Chernobyl accident for which we determined the AMAD fell into two categories: refractory radionuclides (140Ba, 140La 141Ce, 144Ce, 95Zr and 95Nb) and volatile radionuclides (134Cs, 137Cs, 103Ru, 106Ru, 131I, and 132Te). The AMAD of the refractory radionuclides was approximately 3 times higher than the AMAD of the volatile radionuclides; nevertheless, the size distributions for volatile radionuclides having a mean AMAD value of 0.51 μm were very close to the distributions after the Fukushima accident. -- Highlights: • AMADs after the Fukushima and Chernobyl accidents in the Czech Rep. were determined. • The mean value of AMADs of the monitored nuclides from the NPP Fukushima was 0.43 μm. • Nuclides from the NPP Chernobyl fell into two categories – refractory and volatile. • The mean value of AMADs of volatile nuclides from the NPP Chernobyl was 0.51 μm. • AMADs of volatile nucl. from the NPP Chernobyl were 3× smaller than of the refractory radionuclides

  3. Environmental and health consequences in Japan due to the accident at Chernobyl nuclear reactor plant

    A comprehensive review was made on the results of national monitoring program for environmental radioactivity in Japan resulting from the accident at the Chernobyl nuclear power plant in USSR. Period of monitoring efforts covered by the present review is from 30th of April 1986 to 31st of May 1987. A radioactive cloud released from the Chernobyl nuclear reactor initially arrived in Japan on 30th of April 1986 as indicated by the elevated level of 131I, 137Cs and 134Cs activity in the total deposition on 30th of April and also by the increased 137Cs body burden noted on 1st of May. Almost all the radioactive nuclides detected in the European countries were also identified in Japan. For example, the observed nuclides were: 95Zr, 95Nb, 99mTc, 103Ru, 106Ru, 110mAg, 111Ag, 125Sb, 127Sb, 129mTe, 131I, 132Te, 132I, 133I, 134Cs, 136Cs, 137Cs, 140Ba, 140La, 141Ce and 144Ce. Among the above radionuclides, the country average concentration was determined for 131I, 137Cs and 134Cs in various environmental materials such as air, fresh water, soil, milk, leafy and root vegetables, cereals, marine products and other foodstuffs. In contrast to the sharp decline of 131I which was negligible after a few months, 137Cs showed a tendency to maintain its activity in foodstuffs at an appreciable level one year later. Collective effective dose equivalent and dose equivalent to thyroid in Japanese population due to 137Cs, 134Cs and 131I were estimated to be around 590 man Sv and 4760 man Sv, respectively. Corresponding values for the per caput dose equivalent are 5 μSv for whole body and 40 μSv for thyroid, respectively. (author)

  4. Pollution of atmospheric air with toxic and radioactive particulate matter investigated by means of nuclear techniques

    The application of spectrometric methods of nuclear techniques to the investigations of atmospheric air pollution by toxic and radioactive elements and results of these investigations conducted in the highly industrialized and urbanized regions of Poland have been presented. The method of precipitation of the samples, the measurements and analysis of radiation spectra of alpha and gamma radiation emitted by isotopes present in the samples have been described. The concentrations of toxic metal dust in the air have been evaluated by neutron activation and X-ray fluorescence analysis. Appropriate methods of measurement, calibration of instrument and the discussion of results have been presented. The work presents the results of investigations performed in Siersza within the years 1973-1974 and in Warsaw in the period of 1975-1977, which have permitted to estimate the mean monthly values of concentration in the atmospheric air of the following radioisotopes: 7Be, 54Mn, 95Zr, 103Ru, 106Ru, 125Sb, 131I, 137Cs, 140Ba, 141Ce, 144Ce, 226Ra, Th-nat, U-nat and the following stable elements: Sc, Cr, Fe, Co, Zn, As, Se, Sb, W, Pb. The analysis of changes in concentration of each particular artificial radioisotope in the air for the region of Poland in connection with Chinese nuclear explosions have been given. On the basis of the performed environmental investigations the method of analysis of relations between the concentrations of particular elements present in the dust has been discussed. The applications of this method have been presented. The hazard to the population and the environment caused by the radioactive and toxic dust present in the atmospheric air has been estimated. (author)

  5. Separation of plutonium from uranium and fission products in the zirconium pyrophospate column

    Distribution coefficients were of the following ions were determined in the system zirconium pyrophosphate - aqueous solution HNO3 : Pu3+, Pu4+, PuO22+, UO22+, 234Th2+, 95Zr, 95Nb, 106Ru, 144Ce3+, 90Sr2+, 137Cs+, 59Fe3+ and 59Fe2+. According to the distribution coefficients it can be concluded that the separation of some cations is possible. This was proved by using separation columns. The following successful separations were completed: 90Sr2+ from 90I3+, 90Sr2+ from 90I3+ and 1'37Cs+, UO2+ from 234Th4+, Pu4+ from UO22+, 95Zr, 95Nb, 106Ru, 144Ce3+, 90Sr2+, 137Cs+. Decontamination factors of plutonium from the mentioned cations were determined. It was found that the sorption of Cs+ and Sr2+ is based on ion exchange

  6. Yield-Energy Dependence for 147Nd and 144Ce Under Strong Neutron Field

    QIAN; Jing; LIU; Ting-jin; SUN; Zheng-jun; SHU; Neng-chuan

    2012-01-01

    <正>The data of the fission product yield play an important role in the nuclear science technology and nuclear engineering because they are the key data in the calculation of the decay heat, shield design, nuclear verification, radiochemistry reprocessing and nuclear safety, etc. Especially, it is the essential data in fission power estimation for a fission device. It is well known that there exists a consecutive neutron spectrum with the energy from 1 keV to 15 MeV for a fission-fusion device. So in order to estimate the

  7. Sorption of radionuclides from Pb-Bi melt. Report 1

    Results of laboratory investigations of sorption and interfacial distribution of 54Mn, 59Fe, 60Co, 106Ru, 125Sb, 137Cs, 144Ce, 154,155Eu and 235,238U radionuclides in the system Pb-Bi melt - steel surface are analyzed. It is shown that 106Ru and 125Sb are concentrated in Pb-Bi melt and other radionuclides with higher oxygen affinity are sorbed on oxide deposits on structural materials. Temperature dependences of sorption efficiency of radionuclides are studied. It is shown that there is sharp increase of this value for all radionuclides near the temperature range 350-400 deg C. Recommendations are given on the use of 106Ru and 125Sb as a reference for fuel element rupture detection system with radiometric monitoring of coolant melt samples and 137Cs, 134Cs, 134mCs with radiometric monitoring of sorbing samples

  8. Radionuclides contamination of fungi after accident on the Chernobyl NPP

    Zarubina, Nataliia E.; Zarubin, Oleg L. [Institute for Nuclear Research of National Academy of Sciense, 03680, pr-t Nauki, 47, Kiev (Ukraine)

    2014-07-01

    Accumulation of radionuclides by the higher fungi (macromycetes) after the accident on the Chernobyl atomic power plant in 1986 has been studied. Researches were spent in territory of the Chernobyl alienation zone and the Kiev region. Our research has shown that macromycetes accumulate almost all types of radionuclides originating from the accident ({sup 131}I, {sup 140}Ba /{sup 140}La, {sup 103}Ru, {sup 106}Ru, {sup 141}Ce, {sup 144}Ce, {sup 95}Nb, {sup 95}Zr, {sup 137}Cs and {sup 134}Cs). They accumulate the long-living {sup 90}Sr in much smaller (to 3 - 4 orders) quantities than {sup 137}Cs. We have established existence of two stages in accumulation of {sup 137}Cs by higher fungi after the accident on the Chernobyl NPP: the first stage resides in the growth of the concentration, the second - in gradual decrease of levels of specific activity of this radionuclide. Despite reduction of {sup 137}Cs specific activity level, the content of this radionuclide at testing areas of the 5-km zone around the Chernobyl NPP reaches 1,100,000 Bq/kg of fresh weight in 2013. We investigated dynamics of accumulation of Cs-137 in higher fungi of different ecological groups. One of the major factors that influence levels of accumulation of {sup 137}Cs by fungi is their nutritional type (ecological group). Fungi that belong to ecological groups of saprotrophes and xylotrophes accumulate this radionuclide in much smaller quantities than symbio-trophic fungi. As a result of the conducted research it has been established that symbio-trophic fungi store more {sup 137}Cs than any other biological objects in forest ecosystems. Among the symbio-trophic fungi species, species showing the highest level of {sup 137}Cs contamination vary in different periods of time after the deposition. It is connected with variability of quantities of these radio nuclides accessible for absorption at the depth of localization of the main part of mycelium of each species in a soil profile. Soil contamination

  9. Radionuclides contamination of fungi after accident on the Chernobyl NPP

    Accumulation of radionuclides by the higher fungi (macromycetes) after the accident on the Chernobyl atomic power plant in 1986 has been studied. Researches were spent in territory of the Chernobyl alienation zone and the Kiev region. Our research has shown that macromycetes accumulate almost all types of radionuclides originating from the accident (131I, 140Ba /140La, 103Ru, 106Ru, 141Ce, 144Ce, 95Nb, 95Zr, 137Cs and 134Cs). They accumulate the long-living 90Sr in much smaller (to 3 - 4 orders) quantities than 137Cs. We have established existence of two stages in accumulation of 137Cs by higher fungi after the accident on the Chernobyl NPP: the first stage resides in the growth of the concentration, the second - in gradual decrease of levels of specific activity of this radionuclide. Despite reduction of 137Cs specific activity level, the content of this radionuclide at testing areas of the 5-km zone around the Chernobyl NPP reaches 1,100,000 Bq/kg of fresh weight in 2013. We investigated dynamics of accumulation of Cs-137 in higher fungi of different ecological groups. One of the major factors that influence levels of accumulation of 137Cs by fungi is their nutritional type (ecological group). Fungi that belong to ecological groups of saprotrophes and xylotrophes accumulate this radionuclide in much smaller quantities than symbio-trophic fungi. As a result of the conducted research it has been established that symbio-trophic fungi store more 137Cs than any other biological objects in forest ecosystems. Among the symbio-trophic fungi species, species showing the highest level of 137Cs contamination vary in different periods of time after the deposition. It is connected with variability of quantities of these radio nuclides accessible for absorption at the depth of localization of the main part of mycelium of each species in a soil profile. Soil contamination by 137Cs is one of the principal abiotic influences on the accumulation of this radionuclide by fungi

  10. [Comparative analysis of the radionuclide composition in fallout after the Chernobyl and the Fukushima accidents].

    Kotenko, K V; Shinkarev, S M; Abramov, Iu V; Granovskaia, E O; Iatsenko, V N; Gavrilin, Iu I; Margulis, U Ia; Garetskaia, O S; Imanaka, T; Khoshi, M

    2012-01-01

    The nuclear accident occurred at Fukushima Dai-ichi Nuclear Power Plant (NPP) (March 11, 2011) similarly to the accident at the Chernobyl NPP (April 26, 1986) is related to the level 7 of the INES. It is of interest to make an analysis of the radionuclide composition of the fallout following the both accidents. The results of the spectrometric measurements were used in that comparative analysis. Two areas following the Chernobyl accident were considered: (1) the near zone of the fallout - the Belarusian part of the central spot extended up to 60 km around the Chernobyl NPS and (2) the far zone of the fallout--the "Gomel-Mogilev" spot centered 200 km to the north-northeast of the damaged reactor. In the case of Fukushima accident the near zone up to about 60 km considered. The comparative analysis has been done with respect to refractory radionuclides (95Zr, 95Nb, 141Ce, 144Ce), as well as to the intermediate and volatile radionuclides 103Ru, 106Ru, 131I, 134Cs, 137Cs, 140La, 140Ba and the results of such a comparison have been discussed. With respect to exposure to the public the most important radionuclides are 131I and 137Cs. For the both accidents the ratios of 131I/137Cs in the considered soil samples are in the similar ranges: (3-50) for the Chernobyl samples and (5-70) for the Fukushima samples. Similarly to the Chernobyl accident a clear tendency that the ratio of 131I/137Cs in the fallout decreases with the increase of the ground deposition density of 137Cs within the trace related to a radioactive cloud has been identified for the Fukushima accident. It looks like this is a universal tendency for the ratio of 131I/137Cs versus the 137Cs ground deposition density in the fallout along the trace of a radioactive cloud as a result of a heavy accident at the NPP with radionuclides releases into the environment. This tendency is important for an objective reconstruction of 131I fallout based on the results of 137Cs measurements of soil samples carried out at

  11. Oral Zn-DTPA therapy for reducing 141Ce retention in suckling rats

    In neonatal rats DTPA reduced the intestinal retention of cerium ingested as an additive in its chloride form to milk. It also reduced retention of absorbed cerium. A similar decrease of cerium retention in gut and whole body was obtained after simultaneous or 24 hours' delayed DTPA administration. (author)

  12. Fission product release from ZrC-coated fuel particles during postirradiation heating at 1600 C

    Release behavior of fission products from ZrC-coated UO2 particles was studied by a postirradiation heating test at 1600 C (1873 K) for 4500 h and subsequent postheating examinations. The fission gas release monitoring and the postheating examinations revealed that no pressure vessel failure occurred in the test. Ceramographic observations showed no palladium attack and thermal degradation of ZrC. Fission products of 137Cs, 134Cs, 106Ru, 144Ce, 154Eu and 155Eu were released from the coated particles through the coating layers during the postirradiation heating. Diffusion coefficients of 137Cs and 106Ru in the ZrC coating layer were evaluated from the release curves based on a diffusion model. 137Cs retentiveness of the ZrC coating layer was much better than that of the SiC coating layer. ((orig.))

  13. Measurement of leaching from simulated nuclear-waste glass using radiotracers

    The use of radiotracer spiking as a method of measuring the leaching from simulated nuclear-waste glass is shown to give results comparable with other analytical detection methods. The leaching behavior of 85Sr, 106Ru, 133Ba, 137Cs, 141Ce, 152Eu, and other isotopes is measured for several defense waste glasses. These tests show that radiotracer spiking is a sensitive, multielement technique that can provide leaching data, for actual waste elements, that are difficult to obtain by other methods. Additionally, a detailed procedure is described that allows spiked glass to be prepared with a suitable distribution of radionuclides

  14. Three-dimensional plume dynamics in the vadose zone: PORFLO-3 modeling of a defense waste leak at Hanford

    In 1973, approximately 450 m3 of liquid containing radioactive and chemical wastes leaked from the 241-T-106 single-shell tank into the vadose zone at the US Department of Energy's Hanford Site in south-central Washington State. The extent of the 137Cs, 144Ce, and 106Ru contaminant plumes in the vadose zone was estimated in 1973 and 1978 by gamma spectrometry in monitoring wells. Using site data and the PORFLO-3 computer model, a three-dimensional, transient plume migration model was developed for 106Ru and 137Cs. The model was calibrated to the 1973 measured plumes of 106Ru and 137Cs. The calibrated model was then used to study plume migration up to 1990. The simulated 106Ru distribution for 1978 extended deeper than reported values. The simulated distribution of 137Cs for 1978 approximated the measured distribution; the 1973 and 1978 137Cs distributions are similar because of the long half-life and high sorption coefficient of 137Cs. 8 figs., 15 refs

  15. Influence of complex formation on extraction of some fission products by sorption on inorganic sorbents

    Sorption of fission products of radionuclides 137Cs, 89,90Sr, 90,91Y, 86Rb, 133Ba, 95Zr+95Nb, 95Nb, 103,106Ru, 141,144Ce, 115mCd, 113Sn, 125Sb by hydroxides Fe(III), Mn(IV) on the background of 1 mol/l of NaNO3 at the pretense of ions SO42-, C2O42- at a wide ph range (1+14) is studied in present work. Optimal conditions of extraction of each radionuclide by sorption on inorganic sorbents are defined.

  16. Behaviour of solid fission products in the HTGR coated fuel particles

    Results of profile measurements for volume concentrations of 134,137Cs, 144Ce, 155Eu, 106Ru and fissionable material in the HTGR coated fuel particles which have been subjected to standard tests in the temperature range of 1273-2133 K and at burnup up to 17% fima are presented. Values of the effective coefficients of cesium diffusion in kern and protective coating of fuel particles which were subjected to standard in-pile tests in spherical fuel elements at the temperature of 1273 K and the burnup up to 15% fima as well as the value of relative release of solid fission products from the samples studied are given

  17. Dynamics of contents and organic forms of radionuclide compounds in the liquid phase of forest soils in the zone of contamination from the Chernobyl Nuclear Power Plant

    In the profile of forest soils in a 30-km zone around the Chernobyl nuclear power plant (NPP), in areas characterized by different positions in relation to the source of emission, the authors determined the relative contents of long-lived radionuclides 106Ru, 134,137Cs, and 144Ce in soil solutions (as of 1987). On the example of 137Cs, they consider the dynamics (1987-1990) of relative contents and forms in which the radionuclide is found in the liquid phase of soils in the zone of radioactive contamination from the Chernobyl NPP

  18. Silviculture-ecological consequences of forest pollution due to radioactive effluents

    Radioactive contamination effect on the forest areas of Pripyat' Polessie is considered. Radiation processes in damaged pinetree plantations are characterized. Radionuclide migration dependent on soil types and tree stocks is analyzed. The data analysis has shown the evidence of 144Ce, 1'37Cs, 134Cs, 106Ru in 3 years after radioactive contamination in the controlled area. By the end of the third year a significant radionuclide migration had occurred between the forest floor and lower aquifers. refs. 2; figs. 2; tabs. 8

  19. Proposed Search for a Fourth Neutrino with a PBq Antineutrino Source

    Several observed anomalies in neutrino oscillation data can be explained by a hypothetical fourth neutrino separated from the three standard neutrinos by a squared mass difference of a few eV2. We show that this hypothesis can be tested with a PBq (ten kilocurie scale) 144Ce or 106Ru antineutrino beta source deployed at the center of a large low background liquid scintillator detector. In particular, the compact size of such a source could yield an energy-dependent oscillating pattern in event spatial distribution that would unambiguously determine neutrino mass differences and mixing angles.

  20. 1. Quarterly progress report 1984

    This report of the SCPRI exposes an interpretation of the principal results concerning the surveillance of radioactivity in the environment: atmospheric dusts, rainwater, surface water, underground water, sewage water, drinking water, food chain, sea water around nuclear plant sites and other sites. The activities of various radioisotopes are presented in tables (7Be, 54Mn, 58Co, 60Co, 90Sr, 95Nb, 106Ru, 110Ag, 125Sb, 131I, 134Cs, 137Cs, 144Ce, 226Ra, U, K, T and Rn). This report exposes also the state of surveillance and assistance operations on work sites and, the state of incidents along the three months; a bibliographic selection is also presented

  1. Characterization of Inner Tracker silicon prototype sensors using a 106 Ru-source and a 1083 nm laser system

    Bauer, C; Pugatch, V; Schmelling, M; Schwingenheuer, B; Sievers, P

    2001-01-01

    Silicon strip sensors will be used as technology for the LHCb Inner Tracker. The signal-to-noise ratio (S/N) and the charge division among two neighbouring strips are important sensor parameters. In order to investigate the charge sharing between two adjacent strips, measurements with a 1083 nm laser were performed. Minimum ionizing electrons from a ruthenium-source were used to study the S/N-performance of the silicon sensors. The S/N-measurements were also performed with sensors after irradiation with 24 GeV protons up to a fluence of 1.7*10^14 cm^-2, corresponding to more than 10 years of LHCb Inner Tracker operation in the most irradiated zones.

  2. Measurement of dose rate from 106Ru/106Rh ophthalmic applicators by means of alanine-polymer foils

    Ophthalmic applicators are used in radiotherapy for the treatment of malignant choroidal melanomas. The applicators are positioned on the eye at the base of the tumor for a period of a few days up to 2 weeks. They are commercially available in the form of caps of a spherical radius of 12 or 13 mm. Two or three fixing lugs are used for suturing the applicator to the eye. The applicators are made of silver. The active layer is covered with 0.1 mm silver in the concave direction, and 0.9 mm silver in the convex direction. The β-radiation emitted from the concave side may be used for treatment, to a depth up to 5 mm. Measurements of dose rate by means of ESR/alanine dosimetry and TLD are described. It is concluded that ESR/dosimetry and TLD are well suited for this application. (author)

  3. A Dosimetry of 106-Ru - 106- Rh Electron-Photon Field with LiF TLD-100 'Microcubes'

    Background and purpose: Ru-Rh eye applicators are used for the radiotherapy of eye malignancies such as melanomas. The producer (BEBIG GmbH) declares ±30% dose uncertainty in the applicator certificate. There is an obvious need to overcome this large imprecision. Our goal is to establish a method that is fast and reliable and which reduces dose uncertainty to below ±10%. Materials and methods: A pleksiglas phantom containing spherical calottes was constructed for this purpose. It allows measurements of surface homogeneity, absolute surface dose rates and depth doses in 2 mm steps, on and off the symmetry axis. Very small, 1x1x1 mm3 thermoluminescent dosimeters (TLD) were chosen as dosimeters. They have to be calibrated adequately for Ru-Rh dosimetry. To do that, 60Co/electron field response ratio of TLDs was investigated and correction factors were established. Doses to the base of optic nerve were considered. Results: The 60Co/electron beam response ratio of TLDs is in agreement with measured and calculated results reported by other authors (for LiF TLD-100 of different dimensions). The measurements of surface dose rate homogeneity show deviations of up to 15% of the mean surface dose rate. However, surface inhomogeneities average out deeper in the phantom. Absolute surface dose rates were found lower than those declared by the producer by 6.2%, averaged over 8 applicators investigated. On and off axis depth doses are highly uniform over angle θ=40 degrees from symmetry axis, up to 6 mm in depth. Therefore, depth doses form spherical isodose surfaces within stated angle, spanning at least 1.47 steradians. Depth dose functions were interpolated to the measured data for practical routine use. Conclusions: The method developed here has overall combined uncertainty <±6%, and therefore reduces significantly uncertainty declared by the producer. Also, it proved to be stable on repeated measurements. (author)

  4. Concentration and depuration of some radionuclides present in a chronically exposed population of mussels (Mytilus edulis)

    Factors are described which affect the concentration (p Ci g-1 dry wt) and loss of 241 Am, 239+240Pu, 238Pu, 144Ce, 137Cs, 134Cs, 106Ru, 95Zr and 95Nb in an exposed population of mussels Mytilus edulis L. from Ravenglass on the Esk estuary, Cumbria, UK which receives radioeffluents from the British Nuclear Fuels Ltd. (BNFL) plant at Sellafield, some 10 km to the north. Tidal position and mussel body size have a negligible influence on the concentration of 241Am, 137Cs and 106Ru in the total soft tissue, but variation in soft tissue weight throughout the year has a considerable influence on the apparent concentration and depuration times of these radionuclides. Apart from the clearance (tsub(1/2) biol, 1 to 3 h) of sediment-associated activity from the digestive tract, the depuration rate profiles follow a single component clearance curve with a biological half-life in excess of 200 d for 241 Am, 239+240Pu, 238Pu and 144Ce, and of 40 d for 137Cs. The clearance of 106Ru is more complex and consists of a 3 component depuration profile with biological half-lives of 6 h, 12 d and 260 d. The depuration profiles presented in this work are for chronically ingested isotopes under natural conditions; acute exposure will most likely result in different profiles, especially those derived from laboratory spiking experiments. Isotope ratio data support the hypothesis that the main route of entry into the mussel for the majority of the radionuclides studied is from the water. (orig./WL)

  5. Development of removal methods of radioactive ruthenium by using the column packed with cell materials

    Ruthenium is an element of various valencies and present in many chemical species of nitro-nitrosyl complexes in nitric acid or in solutions containing nitrates. Since radioactive ruthenium (103Ru, 106Ru) of those chamical species is contained in the wastes occurred on the fuel reprocessing by Purex method and others, it is one of the nuclides which are most difficult to be removed by the conventional methods of the radioactive waste treatments. It was found that this nuclide was effectively removed by passing the waste solution through a column packed with the mixture of powder of anode and cathode materials and depolarizers used in the electric cells. The typical mixtures were zinc-charcoal, zinc.palladium-charcoal, zinc-manganese dioxide.charcoal and zinc-carbon fluoride.charcoal. These column methods showed a surpassing removel efficiency for 106Ru complexes and fisson products. The decontamination factors of radioactive ruthenium were 104 for all kinds of ruthenium complexes and 102 for the species not easily removed by the conventional methods. It was also found that the concentrations of 239Pu, U, 144ce, 155Eu, and 125Sb in the waste could be decreased to that below the limits of detection by the cell material columns. Because 106Ru of chemical species which was difficult to be removed by conventional methods could be efficiently separated from the waste solutions, it was concluded that the columns packed with cell materials are valuable tools in the radioactive waste treatments. (author)

  6. Behaviour of the radionuclides 125J, 85Sr, 134Cs and 144Ce in three typical sands of Northern Germany under conditions of water-unsaturated flow

    The investigations described in this study help to explain the migration of radionuclides, being in the seepage water, in the upper soil layers. We investigated the behaviour of the radionuclides of the elements J, Sr, Cs and Ce in three types of loose rocks taken from the C-horizon of characteristic soils existing in the surroundings of Gorleben (Lower Saxony). These loose rocks are medium- and fine-grained sands. In the laboratory we performed Batch and column experiments under the conditions of water-unsaturated flow. For these investigations we used an experimental rainwater, which we had prepared on the basis of the analytic mean values obtained for the rainwater of the Gorleben surroundings. (orig./RW)

  7. Studies on inorganic exchangers - manganese dioxide

    As a part of investigation of separation processes for long lived fission products from fuel reprocessing solution, manganese dioxide has been studied as an ion exchanger for cerium using 137Cs, 106Ru, 141Ce, sup(85,89)Sr, 95Zr and 95Nb as tracers. For different concentrations of HNO3, distribution ratios and breakthrough capacities were determined. Cerium was eluted by manganese sulphate and nitric acid. Results show that : (1) at all acidities cerium is adsorbed with almost no uptake of other rare earths, sodium, uranium and plutonium, (2) Ce (IV) gives better adsorption than Ce(III), (3) a combination of manganese sulphate (1 mg/ml) and 3M nitric acid elutes 99% cerium in 5-6 column volumes and (4) as for effect of absorption-elution cycles on MnO2 column, initially there is a decrease in capacity of cerium uptake but thereafter the capacity remains constant. (M.G.B.)

  8. Measurements of fission product concentrations in surface air at Bombay, India, during the period 1975-1981

    Measurements on airborne fallout radioactivity for the period 1975 up to the middle of 1981 are given. Normally, these measurements are confined to Bombay, but after nuclear tests, some of the other stations where these measurements were carried out in previous years are operated for some time to study the levels of fresh activity. The levels of the long-lived fission products 144Ce, 106Ru and 137Cs, and the short-lived fission products 95Zr and 140Ba, were measured, whenever they could be detected following nuclear tests, and tabulated. The data indicate that the activity varies by large factors from tests of similar yield, depending on the meteorological and other conditions. It was determined that the travel time for the Chinese test debris from Lop Nor, China to the West-coast of India is 14 to 16 days

  9. Preparative electrophoresis of industrial fission product solutions

    The aim of this work is to contribute to the development of the continuous electrophoresis technique while studying its application in the preparative electrophoresis of industrial fission product solutions. The apparatus described is original. It was built for the purposes of the investigation and proved very reliable in operation. The experimental conditions necessary to maintain and supervise the apparatus in a state of equilibrium are examined in detail; their stability is an important factor, indispensable to the correct performance of an experiment. By subjecting an industrial solution of fission products to preparative electrophoresis it is possible, according to the experimental conditions, to prepare carrier-free radioelements of radiochemical purity (from 5 to 7 radioelements): 137Cs, 90Sr, 141+144Ce, 91Y, 95Nb, 95Zr, 103+106Ru. (author)

  10. Game as a bioindicator of the radiocontamination

    Natural and artificially produced radionuclides were determined in meat and bones of deer, boar and wild hare on hunting areas in Vojvodina (Serbia). Seven natural radionuclides and three fission products (235U, 238U, 232Th, 7Be, 144Ce, 40K, 106Ru, 134Cs, 137Cs, 90Sr) were identified in the investigated game samples. The highest contents of the radionuclides were found in bones and meat of boars and the lowes in the bones of fallow-deer. The predominant radionuclides were 40K and 90Sr, for all of the investigated animals and their contents depended strongly upon the game species, organ type and the age of the animal. The examined breeding sites did not appear to have any effect on the radionuclide contents in game, which indicates that the radionuclides were uniformly distributed over the habitat. (author) 5 refs.; 3 tabs

  11. Calculated activities of some isotopes in the RA reactor highly enriched fuel significant for possible environmental contamination - Operational report

    This report contains calculation basis and obtained results of activities for three groups of isotopes in the RA reactor 80% enriched fuel element. The following isotopes are included: 1) 85mKr, 87Kr, 88Kr, 131J, 132J, 133J, 134J, 135J, 133Xe, 138Xe i 138Cs, 2) 89Sr, 90Sr, 91Sr, 92Sr, 95Zr, 97Zr, 103Ru, 105Ru, 106Ru, 129mTe, 134Cs, 137Cs, 140Ba, 144Ce, kao i 3) 238Pu, 239Pu i 240Pu. It was estimated that the fuel is exposed to mean neutron flux. The periodicity of reactor operation is taken into account. Calculation results are given dependent on the time of exposure. These results are to be used as source data for Ra reactor safety analyses

  12. Transuranic elements and strontium-90 in samples from forests in Poland

    Enhanced levels of non-volatile nuclides;141,144Ce, 95Zr, 95Nb, 103,106Ru, 238,239,240,241Pu, 241Am, 242,243,244Cm and 154,155Eu were observed in the samples from north-western Poland. This was considered to be a result of finding in sample ''hot particle''. Investigations conducted in the Institute of Nuclear Physics allowed us to conclude that on this area a non typical isotopic composition of Chernobyl fallout was very common. The enhanced activities (up to 100% above the global fallout value) of 90Sr, 238,239,240Pu and 241Am were observed. The presence of 243,244Cm and 154,155Eu was confirmed. It seems that the quasi-continuous fallout of huge numbers of small 'hot particles' occurred there from the high altitude radioactive cloud, which moved toward Scandinavia on 26-th of April, 1986. (author)

  13. The Chernobyl fallout in Greece and its effects on the dating of archaeological materials

    The effects of the fallout from the nuclear reactor accident at Chernobyl have been monitored at various sites in Greece. Here we present the first estimates of gamma dose rates, an essential parameter in the dating of archaeological materials by thermoluminescence (TL) and ESR methods. The dose rates are derived from the long-lived radionuclides of 137Cs, 134Cs, 106Ru and 144Ce (with t1/2 ≥ 1 yr). The present dose rates vary between 30 and 60 mrad/yr, but maximum values of around 811 mrad/yr have also been recorded, for ground-surface exposures. These dose rate values must be regarded as very significant to TL and ESR dating of samples from now on and a correction factor should be applied. (orig.)

  14. Critical pathway studies for selected radionuclides. Part of a coordinated programme on environmental monitoring for radiological protection in Asia and the Far East

    The programme carried out critical pathway studies for selected radionuclides (60Co, 63Ni, 59Fe, 54Mn, sup(110m)Ag, 106Ru and 144Ce) and assessed population exposure in the vicinity of Tarapur Atomic Power Station. The following topics are covered under the programme. (i) Demographic study of dietary habits and consumption data for Tarapur population. (ii) Concentration and accumulation of radionuclides in food products. (iii) Determination of radionuclides in sea water, silt, marine algae and marine organisms at Tarapur Atomic Power Station (TAPS) Site. (iv) Behaviour of radionuclides released to marine environment. (v) Evaluation of critical exposure pathway. (vi) Population exposure in the vicinity of Tarapur Atomic Power Station

  15. Batch extraction studies for the recovery of 233U from thoria irradiated in PHWR

    Batch equilibrium studies were carried out to optimise the extraction parameters for the recovery of 233U from thoria irradiated in PHWR. The thorium concentration and the acidity of the feed was adjusted to ca. 100 g/l and 4 M nitric acid respectively. The concentration of uranium was in the range of 1.4 g/L and it contained long lived fission product like 144Ce-144Pr, 134Cs, 137Cs, 106Ru-106Rh, 105Eu, 154Eu, 90Sr-90Y and 125Sb. 3% TBP in dodecane was used as the solvent. Four stages of batch extraction was followed by a single scrub stage of 4 M nitric acid. The scrubbed organic was stripped with 0.01 M HNO3 thrice. The stripped product was concentrated by evaporation and passed through a cation exchanger to remove the residual thorium. The results of the studies are discussed in detail. (author)

  16. Application of the radiochemical - and the direct gamma ray spectrometry method to the burnup determination of irradiated uranium oxide

    The burn up of natural U3O8 that occurs by the action of thermal neutrons was determined, using the radioisotopes 144Ce, 137Cs, 103Ru, 106Ru and 95Zr as monitors. The determination of the burn up was made using both destructive and non-destructive methods. In the non-destructive method, the technique of direct gamma-ray spectrometry was used and the radioisotopes mentioned were simultaneously counted in a Ge-Li detector. In the radiochemical method the same radioisotopes were isolated one from the other and from all other fission products before counting. The solvent extraction technique was used for the radiochemical separation of uranium, cerium, cesium and ruthenium. To separate zirconium and niobium, adsorption in silica-gel was used. The extraction agent employed to isolate cesium was dipycrilamine and for the separation of the other radioisotopes Di-(2-Ethyl Hexyl) Phosphoric acid (HDEHP) was used. (Author)

  17. Radiation accidents on human in the nuclear installations and their medical emergency procedures, (1)

    Present nuclear installations are one of the safest installations among industrial facilities, being equipped with various safety instruments. Since X-ray was discovered in 1895, however, many radiation injuries of various degrees and kinds occurred. Among dangerous nuclides often observed as radioactivity pollutions in nuclear installations, the exposure to β-ray such as 90Sr, 106Ru, 95Zr, 131I, 144Ce, etc, is considered to be serious problems. When they affect wounds or are inhaled into lungs, only symptomatic treatment is practicable at present, and usually nothing can be depended upon, but spontaneous eliminating ability. As the mass inhalation of α nuclides, especially transuranium nuclides, is quite dangerous, the treatment by lung-irrigation now under development is most effective as the emergency treatment. When trans-uranium nuclides were accidentally observed from wounds, they should be eliminated by the injection of chelating agent. (Kobatake, H.)

  18. Influence of the complexones on the ionic transfer through cell membranes and the level of radionuclides-metals accumulation in water plants

    The influence of the complexones diethylenetriaminepentaacetic acid (DTPA), ethylenediaminetetraacetic acid (EDTA) and hydroxyethylidenediphosphonic acid (HEDP) with relatively low concentrations (from 0.1 to 50 mg/l) on ionic permeability of cell membranes of Nitellopsis obtusa algae, as well as on the accumulation levels of the radionuclides 144Ce, 106Ru, 90Sr and 137Cs in different species of water plants has been studied. It has been shown that complexones under study (with the concentrations up to 50 mg/l) may reduce accumulation levels of three- and four-valent metals and their radionuclides in water plants. For the plants in natural as well as in artificial nutrient medium, however, the complexones increase the availability of metals, forming with the readibly soluble, mobile complex compounds

  19. 4. Quaterly progress report 1983

    This report of the SCPRI exposes an interpretation of the principal results concerning the surveillance of radioactivity in the environment: atmospheric dusts, rainwater, surface water, underground water, sevrage water, drinking water, food chain, sea water around nuclear plant sites and other sites. The activities of various radioisotopes are presented in tables (7Be, 58Co, 60Co, 75Se, 103Ru, sup(110m)Ag, 124Sb, 125Sb, 134Cs, 137Cs, 144Ce, 90Sr, 95Nb, 106Ru, 226Ra, 54Mn, U, K and T). This report exposes also the state of surveillance and assistance operations on work sites and, the state of incidents along the three months; a bibliographic selection is also presented

  20. Specific processes in solvent extractiotn of radionuclide complexes

    The doctoral thesis discusses the consequences of the radioactive beta transformation in systems liquid-liquid and liquid-ion exchanger, and the effect of the chemical composition of liquid-liquid systems on the distribution of radionuclide traces. A model is derived of radiolysis in two-phase liquid-liquid systems used in nuclear chemical technology. The obtained results are used to suggest the processing of radioactive wastes using the Purex process. For solvent extraction the following radionuclides were used: 59Fe, 95Zr-95Nb, 99Mo, sup(99m)Tc, 99Tc, 103Pd, 137Cs, 141Ce, 144Ce-144Pr, 234Th, and 233Pa. Extraction was carried out at laboratory temperature. 60Co was used as the radiation source. Mainly scintillation spectrometry equipment was used for radiometric analysis. (E.S.)

  1. Characterization of gaseous and particulate effluents from the nuclear vitrification project

    Samples were taken during the second high-level liquid waste vitrification campaign associated with the NWVP. Sample analysis established the following total average emission levels in the undiluted vitrification off-gas stream: 3H - 1.2 μCi/m3, 14C - 0.2 μCi/m3, 129I - 1 nCi/m3, NO/sub x/ - 0.5%, 99Tc - 1.6 pCi/m3, and γ-emitters - 105(γ/s)/m3. The aerosol size distribution is composed almost entirely of particles exhibiting smaller diameters than the minimum value for which absolute filters are rated, with an empirical geometric mean diameter of 0.13 μm and a particle mass concentration of 84.7 pg/cm3. The particulate matter was composed of 106Ru, 125Sb, /sup 125m/Te, 134Cs, 137Cs, 144Ce, 154155Eu and 241Am. The particulate emission levels in the undiluted process off-gas stream were: 106Ru - 44 nCi/m3, 125Sb - 0.52 nCi/m3, /sup 125m/Te - 1.7 nCi/m3, 134Cs - 7.8 nCi/m3, 137Cs - 52 nCi/m3, 144Ce - 0.8 μCi/m3, 154Eu - 0.3 nCi/m3, 155Eu - 0.18 nCi/m3, and 241Am - 0.19 nCi/m3. All these environmental gaseous and airborne emissions level liquid waste were well within PNL waste management guidelines

  2. Cycling of radionuclides and impact of operational releases in the near-shore ecosystem off the west coast of India

    Radioecology of the near-shore environment was investigated at Bombay and Tarapur on the west coast of India. The major radionuclides released from the processing plant at Bombay were 137Cs, 144Ce and 106Ru and were discharged through a pipeline to Bombay Harbour bay. At Tarapur the major radionuclides discharged were 131I, 134Cs, 137Cs and 60Co. After dilution with condenser-coolant sea water, releases were carried out through open channels along the shoreline to the sea. Studies on radionuclide cycling in clam-bed sediment, the indicator type benthic organism Anadara granosa, and the fish gobiid mudskipper in Bombay Harbour bay showed that the effective half-life of 137Cs is short compared with the physical half-life (30 years). This is attributable to the desorption of 137Cs from sediment and the fact that the benthic organism readily equilibrates with its environment. The dose to the benthic organism was calculated to be about 0.06 to 3μGy/h. Desorption of 144Ce and 106Ru was not observed. Investigations at Tarapur showed the effective distribution of radionuclides in sea water, sediment, seaweed and marine organisms. It was observed that the radionuclides discharged were mainly confined to a region 2 km from the outfall. The highest activity found in these matrices was only 7% of the derived maximum permissible concentration. The highest thyroid dose due to 131I by fresh seafood intake was 3% of the permissible dose and the highest whole-body dose due to other radionuclides was only 1% of the permissible dose. (author)

  3. The accumulation of radionuclides by Dreissena polymorpha molluscs - The Accumulation of Radionuclides from Water and Food in the Dreissena polymorpha Mollusks

    Jefanova, O.; Marciulioniene, D. [Nature Research Centre, Akademijos str. 2, LT-08412 Vilnius, Lietuva (Lithuania)

    2014-07-01

    The specific activity of {sup 137}Cs, {sup 60}Co, {sup 54}Mn, {sup 90}Sr was measured in mollusks Dreissena polymorpha samples from lake Drukshiai that is the cooling pond of the Ignalina NPP. Item the accumulation of {sup 137}Cs, {sup 90}Sr, {sup 144}Ce, {sup 106}Ru in the mollusks from water and from phytoplankton which is a part of their diet was evaluated under laboratory conditions. The data of long-term (1991-2009) studies conducted at six monitoring stations of lake Drukshiai show that in 1991 {sup 137}Cs in mollusks Dreissena polymorpha was found only in that lake's area which was influenced by the effluent that got into lake from the industrial drainage channel of Ignalina NPP. In later periods of the investigation the {sup 137}Cs specific activity was detected in mollusks samples which had been collected at other monitoring stations (the aquatory of lake Drukshiai). Meanwhile {sup 60}Co and {sup 54}Mn in Dreissena polymorpha were detected only in that lake's area which was impacted by the industrial drainage channel. The data of long-term investigation show that the major amount of radionuclides has come into lake Drukshiai through the industrial drainage system of Ignalina NPP. Albeit {sup 137}Cs, {sup 90}Sr, {sup 144}Ce, {sup 106}Ru get into the mollusks through a large amount of the water rather than from the food (phytoplankton), therefore the food can also be the main source of radionuclides in the organism of these mollusks in aquatic environment when there are low levels of specific activities of these radionuclides. (authors)

  4. Studies of environmental radioactivity in Cumbria

    Five stations collecting samples of atmospheric deposition were set up in north Cumbria along a line running inland from the coast for about 17 km. Sampling was continuous from September 1980 to September 1981. Monthly samples were analysed for 106Ru, 137Cs, 144Ce, 238Pu, sup(239,240)Pu, 241Am, 7Be and stable Na, Cl and Al. The objective of the work was to measure the deposition of radionuclides as a function of distance from the sea. By estimating the contributions to the deposition of nuclear weapon test material and of the atmospheric discharges from the British Nuclear Fuels plc works at Sellafield, the effects of the transfer to air and land of radionuclides in the sea could be established. The marine radionuclides were due to the discharges to sea from the Sellafield works. The measurements showed that the deposition was largely due to the sea-to-land transfer process. The highest depositions observed were at 20 m from high water mark, the annual values (rounded, in Bq m-2) being 106Ru, 500; 137Cs, 650; plutonium, 70; 241Am, 30. The highest concentrations in rainwater for the radionuclides studied were less than 3 per cent of the fresh water limits (drinking only) GDL values. The highest estimated accumulations in soil due to atmospheric deposition were less than 1 per cent of the limits. (author)

  5. Release behavior of metallic fission products from pyrocarbon-coated uranium-dioxide particles at extremely high temperatures

    Hayashi, Kimio; Fukuda, Kousaku (Japan Atomic Energy Research Inst., Tokai, Ibaraki (Japan). Tokai Research Establishment)

    1990-04-01

    Uranium-dioxide particles coated by pyrocarbon (BISO), which were irradiated at 1,300 {approx} 1,400degC to burnups of ca. 1% FIMA, were heated isochronally and isothermally at temperatures between 1,600 and 2,300degC. Release fractions of {sup 137}Cs, {sup 155}Eu and {sup 106}Ru were larger than 10{sup -2} after heating at 2,000degC for 2 h; the results were in contrast to much smaller release fractions from TRISO particles with intact silicon-carbide (SiC) coating. The release of {sup 137}Cs and {sup 144}Ce from the BISO particle was controlled by diffusion in the dense pyrocarbon layer at temperatures between 1,600 and 2,300degC, while that of {sup 155}Eu and {sup 106}Ru was controlled by diffusion in the fuel kernel above 1,800degC. These results can be used as reference data on release behavior of the fission products from TRISO particles with defective SiC layers. (author).

  6. Release behavior of metallic fission products from pyrocarbon-coated uranium-dioxide particles at extremely high temperatures

    Uranium-dioxide particles coated by pyrocarbon (BISO), which were irradiated at 1,300 ∼ 1,400degC to burnups of ca. 1% FIMA, were heated isochronally and isothermally at temperatures between 1,600 and 2,300degC. Release fractions of 137Cs, 155Eu and 106Ru were larger than 10-2 after heating at 2,000degC for 2 h; the results were in contrast to much smaller release fractions from TRISO particles with intact silicon-carbide (SiC) coating. The release of 137Cs and 144Ce from the BISO particle was controlled by diffusion in the dense pyrocarbon layer at temperatures between 1,600 and 2,300degC, while that of 155Eu and 106Ru was controlled by diffusion in the fuel kernel above 1,800degC. These results can be used as reference data on release behavior of the fission products from TRISO particles with defective SiC layers. (author)

  7. Health risks from radionuclides released into the Clinch River

    The purpose of this work is to estimate off-site radiation doses and health risks (with uncertainties) associated with the release of radionuclides from the X-10 site. Following an initial screening analysis, the exposure pathways of interest included fish ingestion, drinking water ingestion, the ingestion of milk and meat, and external exposure from shoreline sediment. Four representative locations along the Clinch River, from the White Oak Creek Embayment to the city of Kingston, were chosen. The demography of the lower Clinch River supplied information dealing with land use that aided in the determination of sites on which to focus efforts. The locations that proved to be the most significant included Jones Island at Clinch River Mile (CRM) 20.5, Grassy Creek and K-25 (CRM 14), Kingston Steam Plant (CRM 3.5), and the city of Kingston (CRM 0). These areas of interest have historically been and are still primarily agricultural and residential areas. Reference individuals were determined with respect to the pathways involved. The primary radionuclides of interest released from the X-10 facility into the Clinch River via White Oak Creek were identified in the initial screening analysis as 137Cs, 90Sr, 60Co, 106Ru, 144Ce, 131I, 95Zr, and 95Nb. Of these radionuclides, 137Cs, 60Co, 106Ru, 90Sr, 144Ce, 95Zr, and 95Nb were evaluated for their contribution to the external exposure pathway. This study utilized an object-oriented modeling software package that provides an alternative to the spreadsheet, providing graphical influence diagrams to show qualitative structure of models, hierarchical models to organize complicated models into manageable modules, and intelligent arrays with the power to scale up simple models to handle large problems. The doses and risks estimated in this study are not significant enough to cause a detectable increase in health effects in the population. In most cases, the organ does are well below the limits of epidemiological detection (1 to 30

  8. Development of a CMPO based extraction process for partitioning of minor actinides and demonstration with genuine fast reactor fuel solution (155 GWd/Te)

    Antony, M.P.; Kumaresan, R.; Suneesh, A.S. [Indira Gandhi Centre for Atomic Research, Kalpakkam (IN). Fuel Chemistry Div.] (and others)

    2011-07-01

    A method has been developed for partitioning of minor actinides from fast reactor (FR) fuel solution by a TRUEX solvent composed of 0.2 M n-octyl(phenyl)-N,N-diisobutylcarbamoyl-methylphosphine oxide (CMPO)-1.2 M tri-n-butylphosphate (TBP) in n-dodecane (n-DD), and subsequently demonstrated with genuine fast reactor dissolver solution (155 GWd/Te) using a novel 16-stage ejector mixer settler in hot cells. Cesium, plutonium and uranium present in the dissolver solution were removed, prior to minor actinide partitioning, by using ammonium molybdophosphate impregnated XAD-7 (AMP-XAD), methylated poly(4-vinylpyridine) (PVP-Me), and macroporous bifunctional phosphinic acid (MPBPA) resins respectively. Extraction of europium(III) and cerium(III) from simulated and real dissolver solution, and their stripping behavior from loaded organic phase was studied in batch method using various citric acid-nitric acid formulations. Based on these results, partitioning of minor actinides from fast reactor dissolver solution was demonstrated in hot cells. The extraction and stripping profiles of {sup 154}Eu, {sup 144}Ce, {sup 106}Ru and {sup 137}Cs, and mass balance of {sup 241}Am(III) achieved in the demonstration run have been reported in this paper. (orig.)

  9. Development of a CMPO based extraction process for partitioning of minor actinides and demonstration with genuine fast reactor fuel solution (155 GWd/Te)

    A method has been developed for partitioning of minor actinides from fast reactor (FR) fuel solution by a TRUEX solvent composed of 0.2 M n-octyl(phenyl)-N,N-diisobutylcarbamoyl-methylphosphine oxide (CMPO)-1.2 M tri-n-butylphosphate (TBP) in n-dodecane (n-DD), and subsequently demonstrated with genuine fast reactor dissolver solution (155 GWd/Te) using a novel 16-stage ejector mixer settler in hot cells. Cesium, plutonium and uranium present in the dissolver solution were removed, prior to minor actinide partitioning, by using ammonium molybdophosphate impregnated XAD-7 (AMP-XAD), methylated poly(4-vinylpyridine) (PVP-Me), and macroporous bifunctional phosphinic acid (MPBPA) resins respectively. Extraction of europium(III) and cerium(III) from simulated and real dissolver solution, and their stripping behavior from loaded organic phase was studied in batch method using various citric acid-nitric acid formulations. Based on these results, partitioning of minor actinides from fast reactor dissolver solution was demonstrated in hot cells. The extraction and stripping profiles of 154Eu, 144Ce, 106Ru and 137Cs, and mass balance of 241Am(III) achieved in the demonstration run have been reported in this paper. (orig.)

  10. Waste/Rock Interactions Technology Program. Status report on LWR spent-fuel leach tests

    Spent fuels with burnups of 9000, 28,000 and 54,500 MWd/MTU have been leach tested at 250C. Three leach-test procedures (Paige, IAEA and static) were used. IAEA and static tests were conducted in five different solutions: deionized water, sodium bicarbonate, sodium chloride, calcium chloride and Waste Isolation Pilot Plant B brine solutions. Elemental leach data are reported based on the release of 90Sr+90Y, 106Ru, 137Cs, 144Ce, 154Eu, 239+240Pu, 125Sb, 244Cm, 129I, 99Tc, and total uranium. This is the first report on 129I and 99Tc from spent fuel. Termination of the Paige test showed that the plateout (radionuclide adsorption) on the test apparatus had negligible effect on the leach rate of cesium and plutonium, but a major (up to a factor of 50 times) effect on the curium leach rate. Three-hundred additional days of leach testing by the IAEA procedure, from 467 to 769 d, showed a continuation of the leaching trends observed during the first 467 d. Results from the first two static leach test series, 2 and 8 d, gave the 129I and 99Tc release numbers

  11. Extrapolation of experimental data on late effects of low-dose radionuclides in man

    The situation of living of population on radionuclide contamination areas was simulated in the experimental study using white strainless rats of different ages. The significance of age for late stochastic effects of internal radionuclide contamination with low doses of 131I, 137Cs, 144Ce and 106Ru was studied. Some common regularities and differences in late effects formation depending on age were found. Results of the study showed that the number of tumors developed increased in groups of animals exposed at the youngest age. The younger animal at the moment of internal radionuclide contamination, the higher percentage of malignant tumors appeared. It was especially so for tumors of endocrine glands (pituitary, suprarenal,- and thyroid). Differences in late effects formation related to different type of radionuclide distribution within the body were estimated. On the base of extrapolation the conclusion was made that human organism being exposed at early postnatal or pubertal period could be the most radiosensitive (1.5-2.0 or sometimes even 3-5 times higher than adults). Data confirmed the opinion that children are the most critical part of population even in case of low dose radiation exposure. (author)

  12. A study of the decontamination effect of commercial detergents on the skin

    Titanium dioxide paste is generally used as the radiological skin decontaminant in the radiation control area at Japan Nuclear Cycle Development Institute (JNC) Tokai works. It is a typical and proven skin decontaminant in the nuclear industry, but there is a disadvantage in that it has a short shelf life. Recently, many detergents applicable as skin decontaminants have become available in non-nuclear industries such as cosmetics and sanitation. They are easily acquired and have an advantage in that stimulus to the skin is mild, because these products have been developed for the human body. In this study, the decontamination factor of the commercial detergents for each nuclide was examined using imitation skin. Sheets of raw pig skins were contaminated with a nitric-acid solution containing 144Ce, 137Cs, 106Ru or 60Co, and then washed with various detergents such as a neutral detergent, cleansing cream and orange oil. The nuclide removal rates of some of the commercial detergents examined were nearly equal to that of titanium dioxide, thus proving that they show satisfactory decontamination performance as a skin decontaminant. (author)

  13. Reconstruction of radionuclide releases from the Hanford Site, 1944-1972

    Historic releases of key radionuclides were estimated as a first step in determining the radiation doses that results from Hanford Site operations. The Hanford Site was built in southcentral Washington State during World War II to provide plutonium for the U.S. nuclear weapons program. As part of the Hanford Environmental Dose Reconstruction (HERD) Project, releases to the Columbia River of 24Na, 32P, 46Sc, 51Cr, 56Mn, 65Zn, 72Ga, 76As, 90Y, 131I, 239Np, and nonvolatile gross beta activity from operation of eight Hanford single-pass production reactors were estimated. Releases of 90Sr, 103Ru, 106Ru, 131I, 144Ce, and 239Pu to the atmosphere from operation of chemical separation facilities were also estimated. These radionuclides and the atmospheric and Columbia River pathways were selected for study because scoping studies showed them to be the largest contributors to dose from Hanford operations. The highest doses resulted from releases to the atmosphere of 131I from chemical separations plants in the pre-1950 period. Prior to 1950, the technology for limiting iodine releases had not been developed. Hence, a very detailed reconstruction of the hourly 131I release history was achieved for 1944-1949 using Monte Carlo methods. Atmospheric releases of the other radionuclides were estimated on a monthly basis for 1944-1972 using deterministic calculations. Monthly releases to the Columbia River for 1944-1971 were based on Monte Carlo methods

  14. Burn-up determination of irradiated uranium oxide by means of direct gama spectrometry and by radiochemical method

    The burn-up of thermal neutrons irradiated U3O8 (natural uranium) samples has been determined by using both direct gamma spectrometry and radiochemical methods and the results obtained were compared. The fission products 144Ce, 103Ru, 106Ru, 137Cs and 95Zr were chosen as burn-up monitors. In order to isolate the radioisotopes chosen as monitors, a radiochemical separation procedure has been established, in which the solvent extraction technique was used to separate cerium, cesium and ruthenium one from the other and all of them from uranium. The separation between zirconium and niobium and of both elements from the other radioisotopes and uranium was accomplished by means of adsorption on a silica-gel column, followed by selective elution of zirconium and of niobium. When use was made of the direct gamma-ray spectrometry method, the radioactivity of each nuclide of interest was measured in presence of all others. For this purpose use was made of gamma-ray spectrometry and of a Ge-Li detector. Comparison of burn-up values obtained by both methods was made by means of Student's 't' test, and this showed that results obtained in each case are statistically equal. (Author)

  15. Position of sediments in transfer of radionuclides released into coastal sea to human beings

    A great portion of radionuclides released into coastal sea is adsorbed into marine sediments and the adsorbed radionuclides causes the radioactive contamination of marine organisms and then transferred to human beings who consume them. In order to make a quantitative evaluation of this route, the transfer of 9 kinds of radionuclides from sediments to benthic organisms such as algae, bivalve and worm was observed. Then it was compared with the radioactivity in these organisms from radioactively contaminated sea water (Concentration factor). It was observed that the influence of sea water was larger than that of sediments as it was 104 times larger for 54Mn, 103 times larger for 59Fe, 60Co, 95Zr-95Nb, 106Ru-106Rh and 144Ce-144Pr, 102 times larger for 65Zn and 10-102 times larger for 115mCd and 137Cs. Consequently, sea water can be considered as the main route and sediments as the secondary in the case of quantitative comparison of the effect on the accumulation of radionuclides by marine organisms and in the transfer of radionuclides to human beings

  16. Measurement of radionuclides in bricks made from refuse ash of sewage sludge

    Since people spend about 80% of their time in buildings, in order to estimate the radiation exposure dose of nation, it is necessary to grasp indoor dose level. It has been known that as for indoor radiation exposure dose, it is different according to the types of buildings, and generally it is low in wooden houses, and high in concrete and brick buildings. This difference is due to the shielding of environmental radiation by building material and the radiation emitted from building materials themselves. In this study, the radionuclides in the bricks made of sewage slude-incinerated ash and red bricks for the reference were investigated. The radiation emitted from the bricks was measured with a thermoluminescence dosimeter (TLD). The sampling and pretreatment, the measuring method, the measurement of the radiation dose on the bricks, and the results are reported. As for the natural radionuclides in the bricks, 7Be was detected in most sludge bricks, and the concentration varied largely according to the data of sampling. It was not detected in red bricks. 40K, 214Bi and 228Ac were detected in all the sludge and red bricks. Artificial radionuclides such as 54Mn, 60Co, 106Ru, 131I, 134Cs and 144Ce were not detected in all the sludge and red bricks. The radiation dose on the sludge and red bricks was 20.5 - 21.7 mR, and constant regardless of the data of sampling. (K.I.)

  17. Application of radiochemical-and direct gamma ray spectrometry methods for the determination of the burnup of irradiated uranium oxide

    The burn-up of U3O8 (natural uranium) samples was determined by using both destructive and non-destructive methods, and comparing the results obtained. The radioisotopes 144Ce, 103Ru, 106Ru, 137Cs and 95Zr were chosen as monitors. In order to isolate the radioisotopes chosen as monitors, a separation scheme has been established in which the solvent extraction technic is used to separate cerium, cesium, and ruthenium one from the other and from uranium. The separation between zirconium and niobium and of both from the others was accomplished by means of adsorption on a silica-gel column. When the non-destructive method was used, the radioactivity of each nuclide of interest was measured in the presence of all others. For this purpose, use was made of gamma-ray spectrometry and a Ge-Li detector. The comparison of burn-up values obtained by both destructive and non-destructive methods was made by means of Student's 't' test, and it has shown that the averages of results obtained in each case are equal. (Author)

  18. Chernobyl radionuclides in a Black Sea sediment trap.

    Buesseler, K O; Livingston, H D; Honjo, S; Hay, B J; Manganini, S J; Degens, E; Ittekkot, V; Izdar, E; Konuk, T

    The Chernobyl nuclear power station accident released large quantities of vaporized radionuclides, and, to a lesser extent, mechanically released small (less than 1-10 micron) aerosol particles. The total release of radioactivity is estimated to be out of the order of 1-2 x 10(18) Bq (3-5 x 10(7) Ci) not allowing for releases of the xenon and krypton gases. The 137Cs releases of 3.8 x 10(16) Bq from Chernobyl can be compared to 1.3 x 10(18) Bq 137Cs released due to atmospheric nuclear weapons testing. Chernobyl-derived radionuclides can be used as transient tracers to study physical and biogeochemical processes. Initial measurements of fallout Chernobyl radionuclides from a time-series sediment trap at 1,071 m during June-September 1986 in the southern Black Sea are presented. The specific activities of 137Cs, 144Ce and 106Ru in the trap samples (0.5-2, 4-12 and 6-13 Bq g-1) are independent of the particle flux while their relative activities reflect their rates of scavenging in the order Ce greater than Ru greater than Cs. PMID:3670387

  19. Interaction of radionuclides with geomedia associated with the Waste Isolation Pilot Plant (WIPP) site in New Mexico

    A survey of the potential of geological media from the vicinity of the Waste Isolation Pilot Plant site in Southeastern New Mexico for retardation of radionuclide migration in an aqueous carrier was conducted. The survey included the measurement of sorption coefficients (Kd) for twelve radionuclides between three natural water simulants and ten samples from various geological strata. The nuclides included 137Cs, 85Sr, 131I, 99Tc, 125Sb, 144Ce, 152Eu, 153Gd, 106Ru, 243Am, 244Cm, and 238Pu. The compositions of the simulant solutions were those expected of water in contact with potash minerals or halite deposits in the area and in a typical groundwater found in the Delaware Basin. The geological samples were obtained from potential aquifers above and below the proposed repository horizons and from bedded salt deposits in the repository horizons. In brine solutions, Tc and I were not significantly adsorbed by any of the minerals and Cs and Sr showed minimal adsorption (Kd's 103 and Ru and Sb Kd's varied in the range of 25 to > 103. In the groundwater simulant, Tc and I showed the same behavior, but the Kd's of the other nuclides were generally higher. Some initial parametric studies involving pH, trace organic constituents in the simulant solutions, and radionuclide concentrations were carried out. Significant differences in the observed Kd's can result from varying one or more of these solution parameters

  20. Innovative separation method for advanced spent fuel reprocessing based on tertiary pyridine resin

    Radiochemical separation experiments have been performed in order to realize a novel reprocessing method based on chromatography techniques using a novel pyridine resin. The newly synthesized tertiary pyridine resin with two functions of ion exchanger and soft-donor was dedicated to the experiments, where highly irradiated mixed oxide fuel from the experimental fast reactor JOYO was used as a reference spent fuel. With a 3-step separation, pure Am and Cm were individually obtained as minor actinide products, and 106Ru group, lanthanides with 137Cs group and Pu group were fractionated, respectively. The decontamination factor of 137Cs and trivalent lanthanides (155Eu, 144Ce) against the Am product exceeded 3.9 x 104 and 1.0 x 105, respectively. The decontamination factor as the mutual separation of 243Cm was larger than 2.2 x 103 against the Am product. Moreover, the content of 137Cs, trivalent lanthanides and 243Cm in Am product did not exceed 2 ppm. The tertiary pyridine resin method is a candidate separation system for an 'advanced ORIENT process', where enhanced separation, transmutation and utilization of actinides, long-lived fission products and rare metal fission product would be oriented. (author)

  1. Chemical and physical considerations of the use of nuclear fuel spikants for deterrence

    Selle, J. E.

    1978-10-01

    One proposed method of inhibiting the diversion of nuclear fuel for clandestine purposes is to add to the fuel a highly gamma-active material of such intensity that remote handling equipment is necessary in all stages of handling and reprocessing. This is called spiking for deterrence. The present work sought to identify candidate spikants and identify potential materials problems that might occur as the result of incorporation of these spikants with the fuel. Potential spikants were identified and thermodynamic analysis was performed to determine their chemical and physical states. Phase relationships between spikants (and their decay products) and the fuel constituents were surveyed. According to criteria defined in this report, /sup 60/Co, /sup 106/Ru, and /sup 144/Ce appear to have the greatest potential as spikants. Cerium should be present as the oxide, soluble in the fuel, while cobalt and ruthenium should be present in the metallic state with very low solubility in the fuel. Experimental work on the distribution of fission products and their interactions with cladding was also surveyed to provide information on the distribution of spikants in the fuel and describe the probable effects of spikants on the fuel. Cobalt, ruthenium, and cerium should not present any problems due to reaction with stainless steel cladding.

  2. Neutron cross sections of 28 fission product nuclides adopted in JENDL-1

    This is the final report concerning the evaluated neutron cross sections of 28 fission product nuclides adopted in the first version of Japanese Evaluated Nuclear Data Library (JENDL-1). These 28 nuclides were selected as being most important for fast reactor calculations, and are 90Sr, 93Zr, 95Mo, 97Mo, 99Tc, 101Ru, 102Ru, 103Rh, 104Ru, 105Pd, 106Ru, 107Pd, 109Ag, 129I, 131Xe, 133Cs, 135Cs, 137Cs, 143Nd, 144Ce, 144Nd, 145Nd, 147Pm, 147Sm, 149Sm, 151Sm, 153Eu and 155Eu. The status of the experimental data was reviewed over the whole energy range. The present evaluation was performed on the basis of the measured data with the aid of theoretical calculations. The optical and statical models were used for evaluation of the smooth cross sections. An improved method was developed in treating the multilevel Breit-Wigner formula for the resonance region. Various physical parameters and the level schemes, adopted in the present work are discussed by comparing with those used in the other evaluations such as ENDF/B-IV, CEA, CNEN-2 and RCN-2. Furthermore, the evaluation method and results are described in detail for each nuclide. The evaluated total, capture and inelastic scattering cross sections are compared with the other evaluated data and some recent measured data. Some problems of the present work are pointed out and ways of their improvement are suggested. (author)

  3. Gamma spectrometrical analyses of annual deposition samples collected in Romania in 1987-1989

    The dynamics of artificial radionuclide concentrations in deposition samples in the years 1987-1989 is presented in this paper. High resolution gamma spectrometrical analyses have been performed on wet and dry deposition samples from the following stations of the National Environmental Radioactivity Surveillance Network: Cluj-Napoca, Satu-Mare, Constanta, Ceahlau-Tosca, lasi and Craiova. In order to determine small concentrations of low level artificial radionuclides (having an appropriate half life) yearly samples obtained by cumulating daily samples were measured. The following gamma emitting radionuclides were identified in these samples: 106Ru, 110mAg, 125Sb, 134Cs, 137Cs, 144Ce. It can be seen that the level of radionuclide activities in deposition samples at any time is dependent on the 'initial' deposition of May 1986. An environmental half life of 137Cs in deposition can be assessed. For a particular case the evolution during 1987-1989 of 137Cs and 7Be specific activities in monthly samples is also presented. (author)

  4. Experimental study on biokinetics of radionuclides in age groups

    In the aftermath of the Chernobyl accident, it becomes evident that dose coefficients for members of the public are necessary. International Commission on Radiological Protection (ICRP) established a task group of Committee 2 charged with the assessment of dose coefficients as a function of an individual's age. However, little data is available on the biokinetics of radionuclides in juvenile and is a need to develop age-dependent biokinetic models, such as for the gastrointestinal tract. The present paper reviewed an outline on characteristics of biokinetics of radionuclides in juvenile animals focusing on the previous experimental data. The following radionuclides are discussed: 54Mn, 60Co, 65Zn, 75Se, 106Ru, 110mAg, 115Cd, 125Sb, 137Cs, 141Ce, 203Hg and 3H. Generally, intestinal absorption and whole-body retention of radionuclides in Juveniles were higher than that of adult. In the case of sucklings, it is very important to study how radionuclides are transferred through the placenta and milk. The transfer rate of radionuclides through the placenta and milk is dependent on the period of gestation at the time of dosing. The IDES (Internal Dose Estimation System) which is based on the ICRP model was used for dose calculation. We modified the IDES using the biokinetic data which was gained by animal experiment. The IDES is flexible because the absorbed dose can be calculated by substituting arbitrary physical and physiological parameters and also substituting ingested dose coefficients not only for the ICRP Reference Man, but also for Japanese of 1 year old, 5 years old, 10 years old, 15 years old and the adult, respectively. (author)

  5. Biokinetics and dose assessment of radionuclides in juveniles

    In the aftermath of the Chernobyl accident, it becomes evident that dose coefficients for members of the public are necessary. International Commission on Radiological Protection (ICRP) established a task group of Committee 2 charged with the assessment of dose coefficients as a function of an individual's age. However, little data is available on the biokinetics of radionuclides in juvenile and there is a need to develop age-dependent biokinetic models, such as for the gastrointestinal tract. The present paper reviewed an outline on characteristics of biokinetics of radionuclides in juvenile animals focusing on the previous experimental data. The following radionuclides are discussed: 54Mn, 60Co, 65Zn, 75Se, 106Ru, 110mAg, 115mCd, 125Sb, 137Cs, 141Ce, 203Hg and 3H. Generally, intestinal absorption and whole-body retention of radionuclides in juveniles were higher than that of adult. In the case of sucklings, it is very important to study how radionuclides are transferred through the placenta and milk. The transfer rate of radionuclides through the placenta and milk is dependent on the period of gestation at the time of dosing. The IDES(Internal Dose Estimation System) which is based on the ICRP model was used for dose calculation. We modified the IDES using the biokinetic data which was gained animal experiment. The IDES is flexible because the absorbed dose can be calculated by substituting arbitrary physical and physiological parameters and also substituting ingested dose coefficients not only for the ICRP Reference Man, but also for Japanese of 1 year old, 5 years old, 10 years old, 15 years old and the adult, respectively. (author)

  6. Radioactive contamination of bottom sediments in the upper reaches of the Techa river: analysis of the data obtained in 1950 and 1951.

    Mokrov, Yury G

    2003-10-01

    A stationary sorption model has been developed for re-evaluating and analysing archive data from 1950-1951 on the radioactive contamination of Techa river bottom sediments close to the site of liquid radioactive waste discharge. In general, good agreement was obtained between calculations and measurements, which substantiates further the assumptions and conclusions in two preceding articles, on the radionuclide composition of discharged liquid radioactive waste. Estimates on the effective liquid radioactive waste discharges given here are significantly different from those deduced in the 1950s, i.e. in summer 1950 and October 1951. The results are discussed in relation to the Techa River Dosimetry System 2000 (TRDS-2000) that has recently been presented to serve as a means for estimating doses to the Techa river residents. Parameter values describing the exponential decrease of bottom sediment contamination along the river due to short-lived radionuclides, such as (106)Ru, and (144)Ce, agree reasonably with those used in TRDS-2000. However, for other radionuclides, such as (95)Zr, (95)Nb, (91)Y, (90)Sr and (137)Cs, substantial differences are found. It is demonstrated that water flow rate, width of the river, and surface area of bottom sediments are important parameters which were not adequately taken into account in TRDS-2000. Also, the stirring-up of contaminated bottom sediments and their subsequent transport by the water flow are seen to be an important mechanism that governs the radionuclide transport downstream. This mechanism was not included in the TRDS-2000 model. It is concluded that the sorption model used in TRDS-2000 for the reconstruction of radioactive contamination of water and bottom sediments of the Techa river in 1949-1951, is subject to considerable errors. While the present paper is focussed on details of the dosimetric modelling, the implications for the Techa river dosimetry are major. They will be further elucidated in a forthcoming paper

  7. Determining initial enrichment, burnup, and cooling time of pressurized-water-reactor spent fuel assemblies by analyzing passive gamma spectra measured at the Clab interim-fuel storage facility in Sweden

    Favalli, A.; Vo, D.; Grogan, B.; Jansson, P.; Liljenfeldt, H.; Mozin, V.; Schwalbach, P.; Sjöland, A.; Tobin, S. J.; Trellue, H.; Vaccaro, S.

    2016-06-01

    The purpose of the Next Generation Safeguards Initiative (NGSI)-Spent Fuel (SF) project is to strengthen the technical toolkit of safeguards inspectors and/or other interested parties. The NGSI-SF team is working to achieve the following technical goals more easily and efficiently than in the past using nondestructive assay measurements of spent fuel assemblies: (1) verify the initial enrichment, burnup, and cooling time of facility declaration; (2) detect the diversion or replacement of pins; (3) estimate the plutonium mass [which is also a function of the variables in (1)]; (4) estimate the decay heat; and (5) determine the reactivity of spent fuel assemblies. Since August 2013, a set of measurement campaigns has been conducted at the Central Interim Storage Facility for Spent Nuclear Fuel (Clab), in collaboration with Swedish Nuclear Fuel and Waste Management Company (SKB). One purpose of the measurement campaigns was to acquire passive gamma spectra with high-purity germanium and lanthanum bromide scintillation detectors from Pressurized Water Reactor and Boiling Water Reactor spent fuel assemblies. The absolute 137Cs count rate and the 154Eu/137Cs, 134Cs/137Cs, 106Ru/137Cs, and 144Ce/137Cs isotopic ratios were extracted; these values were used to construct corresponding model functions (which describe each measured quantity's behavior over various combinations of burnup, cooling time, and initial enrichment) and then were used to determine those same quantities in each measured spent fuel assembly. The results obtained in comparison with the operator declared values, as well as the methodology developed, are discussed in detail in the paper.

  8. Passive gamma analysis of the boiling-water-reactor assemblies

    Vo, D.; Favalli, A.; Grogan, B.; Jansson, P.; Liljenfeldt, H.; Mozin, V.; Schwalbach, P.; Sjöland, A.; Tobin, S.; Trellue, H.; Vaccaro, S.

    2016-09-01

    This research focused on the analysis of a set of stationary passive gamma measurements taken on the spent nuclear fuel assemblies from a boiling water reactor (BWR) using pulse height analysis data acquisition. The measurements were performed on 25 different BWR assemblies in 2014 at Sweden's Central Interim Storage Facility for Spent Nuclear Fuel (Clab). This study was performed as part of the Next Generation of Safeguards Initiative-Spent Fuel project to research the application of nondestructive assay (NDA) to spent fuel assemblies. The NGSI-SF team is working to achieve the following technical goals more easily and efficiently than in the past using nondestructive assay (NDA) measurements of spent fuel assemblies: (1) verify the initial enrichment, burnup, and cooling time of facility declaration; (2) detect the diversion or replacement of pins, (3) estimate the plutonium mass, (4) estimate the decay heat, and (5) determine the reactivity of spent fuel assemblies. The final objective of this project is to quantify the capability of several integrated NDA instruments to meet the aforementioned goals using the combined signatures of neutrons, gamma rays, and heat. This report presents a selection of the measured data and summarizes an analysis of the results. Specifically, trends in the count rates measured for spectral lines from the following isotopes were analyzed as a function of the declared burnup and cooling time: 137Cs, 154Eu, 134Cs, and to a lesser extent, 106Ru and 144Ce. From these measured count rates, predictive algorithms were developed to enable the estimation of the burnup and cooling time. Furthermore, these algorithms were benchmarked on a set of assemblies not included in the standard assemblies set used by this research team.

  9. Status report on LWR spent fuel IAEA leach tests

    Spent light-water-reactor (LWR) fuel with an average burnup of 28,000 MWd/MTU was leach-tested at 250C using a modified version of the International Atomic Energy Agency procedure. Leach rates were determined from tests conducted in five different solutions: deionized water, sodium chloride (NaCl), sodium bicarbonate (NaHCO3), calcium chloride (CaCl2) and Waste Isolation Pilot Plant B brine solutions. Elemental leach rates are reported based on the release of 90Sr + 90Y, 106Ru, 137Cs, 144Ce, 154Eu, /sup 239 + 240/Pu, 244Cm and total uranium. After 467 days of cumulative leaching, the elemental leach rates are highest in deionized water. The elemental leach rates uin the different solutions generally decreased from deionized water to the 0.03M NaCl solution to the WIPP B brine solution to the 0.03M NaHCO3 solution and was a factor of 20 lower in 0.015M CaCl2 solution than in deionized water. The leach rates of spent fuel and borosilicate waste-glass were also compared. In sodium bicarbonate solution, the leach rates of the two waste forms were nearly equal, but the glass was increasingly more resistant than spent fuel in calcium chloride solution, followed by sodium chloride solution, WIPP B brine solution and deionized water. In deionized water the glass, based on the elemental release of plutonium and curium, was 50 to 400 times more leach resistant than spent fuel

  10. Transfer of nuclides from the water phase to the sediments during normal and extraordinary hydrological cycles

    Atucha I and Atucha II nuclear power plants are located on the right margin of the Parana de las Palmas river. This river belongs to the Cuenca del Plata, whose 1982-1983 hydrologic cycle registered the greatest freshets of the century. Works and studies previously fixed had to be altered and investigations were adapted to the possibilities and the particular hydric conditions verified. Considerations on the transfer of nuclides between water and sediments are presented. The floods reduce the water-sediments contact time on the bed of the river. In outer areas, the waters labelled by the nuclear power plant effluent discharge favor the infiltration in alluvial soils, as well as the exchange with the sediments. The investigations carried out for the phase near to the discharge of liquid effluents (related to the critical group) made possible to prove the characteristics of the path of the liquid wastes released, the distribution coefficient and the fixation or penetrability of some nuclides in soils of the floody valley. In this manner, a balance of radioactive nuclides incorporated to soils and sediments from the neighbourhood of Atucha and the water-course of Parana de las Palmas river is obtained. The presence of 60Co and 137Cs in the floody soils on the right margin of this river was detected and measured during the greatest flood of the century. On the other hand, 144Ce, 51Cr, 106Ru and 90Sr have not been detected. The detection of artificial radioisotopes turns out to be impossible in normal hydrological years, even in the sorroundings of the nuclear power plant or the critical group (from the point of view of the surface waters, The Fishing Club, 3 km down stream). (M.E.L.)

  11. Estimation of 90Sr activity in reprocessed uranium from the PUREX process

    90Sr estimation in reprocessed uranium was carried out by a series of solvent extraction and carrier precipitation techniques using strontium and lanthanum carriers. Fuming with HClO4 was used to remove 106Ru as RuO4. Three step solvent extraction with 50% tri-n-butyl phosphate in xylene in presence of small amounts of dibutyl phosphate and thenoyl trifluoro acetone was carried out to eliminate uranium, plutonium, thorium and protactinium impurities. Lanthanum oxalate precipitation in acid medium was employed to scavenge the remaining multivalent ions. Strontium was precipitated as strontium oxalate in alkaline pH and 137Cs was removed by washing the precipitate with water. A strontium recovery well above 70% was obtained. Final estimation was carried out by radiometry using end window GM counter after drying the precipitate under an infra red lamp. The same procedure was extended to the estimation of 90Sr in a diluted sample of the actual spent fuel solution. An additional lanthanum oxalate precipitation step was required to remove the entire 144Ce impurity from this sample. This modified procedure was employed in the determination of 90Sr in a number of reprocessed uranium samples and the over all precision of the method was found to be well within ±10%. An additional barium chromate precipitation step was necessary for the analysis of reprocessed uranium samples from high burnup fuels to eliminate trace amounts of short lived 224Ra produced during the decay of 232U and its daughters as they interfere in the estimation of 90Sr. (author)

  12. Oceanographic Survey. 3. Radiological survey of marine environment in Ibaraki Prefecture: marine sediment survey

    Radioactivity in marine environment of Ibaraki Prefecture has been monitored since 1965. This report briefly describes the radiological survey data of marine sediments. The concentrations of radionuclides in marine water were determined yearly 4 times for 3H and twice for 54Mn, 60Co, 90Sr, 95Zr, 95Nb, 106Ru, 137Cs and 144Ce. The concentrations of 90Sr, 137Cs and 239+240Pu were hardly changed and those of 90Sr and 137Cs were near the limit of identification. The annual excretion of radionuclides from major nuclear plants in Ibaraki Prefecture including JAERI (Tokai and Oarai), Japan Atomic Power Co., etc. were determined for 3H, 14C, 90Sr, 137Cs, 60Co, 129I and 239+240Pu. Based on the results, dose equivalent for the intake of marine animals and algae was estimated to be as low as 0-4.4 μSv. This level was extremely lower than the limit of annual dose equivalent; 1000 μSv and it was kept nearly constant if the operators of those facilities were not discontinued for a long. To elucidate the factors related to the transfer of radionuclides into marine sediments, the depth dose distribution in marine sediments were investigated as well as the relation between radionuclide level and granular size. An elevation of 137Cs level was found for the sediments composed of fine granules, which were rich in the sediments of offshore region. The 239+240Pu level was positively correlated to the content of organic compounds in the sea. (M.N.)

  13. Forage: A sensitive indicator for airborne radioactivity

    As a part of the radiological environmental monitoring program at the Joseph M. Parley Nuclear Plant to meet the requirements of NRC Regulations 10 CRF 50, Appendix I, routine sampling of forage was implemented. Indicator plots of forage (grass) were established at the plant site boundary in the two Meteorological sectors having the highest X/Q values for ground-level dispersion of airborne radioactivity. Likewise, a control plot was established in a sector having a significantly lower X/Q value at a distance of 18 miles. Procedures for maintenance of the grass plots, sampling of forage, and sample preparation for measurement of gamma radioactivity with a Ge (Li) detector were developed during the reported three year measurement period. Three atmospheric nuclear tests by the Peoples Republic of China in 1976 and 1977 has proven forage sampling to be convenient, sensitive, and in the judgement of the authors gives results which are superior to most other media sampled for airborne radioactivity. Typical measured levels of radioactivity from 150 to greater than 10,000 pCi/kg (dry weight) were obtained for the principal fission products in the Chinese bomb fallout, which included 95Zr-95Nb, 103Ru, 131I, 140Ba-140La, 141Ce, and 144Ce. On a unit weight basis the level of radioactivity measured was consistently higher for forage than for green leafy vegetables. This was attributed to the higher surface area for the forage. For comparison, plots of airborne concentrations for gross beta and particulate gamma emitters are shown during the time periods that include the Chinese nuclear tests. (author)

  14. Revascularization of calvarial, mandibular, tibial, and iliac bone grafts in rats

    Pinholt, E M; Solheim, E; Talsnes, O;

    1994-01-01

    area of harvest of bone graft is important regarding early revascularization, but the results do not support the theory that different embryological mode of development is the cause since mandibula (high 141Ce index) and calvaria (low 141Ce index) are of membranous origin and iliac bone (high 141Ce...... index) and tibia (low 141Ce index) are of endochondral origin. The difference in revascularization between the different grafts may be explained by differences in quantity of cancellous bone since cancellous bone is revascularized faster than cortical bone....

  15. Results For The Third Quarter 2009 Tank 50 WAC Slurry Sample: Chemical And Radionuclide Contaminant Results

    This report details the chemical and radionuclide contaminant results for the characterization of the 2009 Third Quarter sampling of Tank 50 for the Saltstone Waste Acceptance Criteria (WAC). Information from this characterization will be used by Liquid Waste Operations (LWO) to support the transfer of low-level aqueous waste from Tank 50 to the Salt Feed Tank in the Saltstone Facility in Z-Area, where the waste will be immobilized. This information is also used to update the Tank 50 Waste Characterization System. Recently, a review of the radionuclide inventory in Saltstone Vaults 1 and 4 identified several additional radionuclides, not currently in the WAC, which require quantification (40K, 108mAg, 133Ba, 207Bi, 227Ac, 228Ra, 228Th, 231Pa, 247Cm, 249Cf, 251Cf). In addition, several of the radionuclides previously reported with minimum detection limits below the requirements listed in the WAC required analysis with reduced detection limits to support future inventory reporting requirements (22Na, 26Al, 59Ni, 94Nb, 106Ru, 144Ce, 152Eu, 155Eu, 226Ra). This added scope was formally requested in a revision to the standing Technical Task Request for CY2009 Saltstone support and is further discussed in several supporting documents. The following conclusions are drawn from the analytical results provided in this report: (1) The concentrations of the reported chemical and radioactive contaminants are less than their respective WAC targets or limits unless noted in this section. (2) The reported detection limits for 59Ni, 94Nb, 247Cm, and 249Cf are above the limits requested by LWO; however, they are below the achievable limits established by Analytical Development (AD). (3) The reported detection limit of isopropanol is lower than its WAC Limit for accident analysis in Appendix 8.1, but higher than its WAC concentration given in Table 4 for vault flammability. The higher detection limit is expected based on current analytical capabilities and is documented in the Task

  16. Reconstruction of radionuclide contamination of the Techa River caused by liquid waste discharge from radiochemical production at the Mayak Production Association

    , rather than relying on a more uncertain reconstruction of quantities released at the point of discharge. Radionuclides considered include 90Sr, 106Ru, 137Cs, and 144Ce. Estimated concentrations of selected radionuclides at various times are presented

  17. Reconstruction of radionuclide contamination of the Techa River caused by liquid waste discharge from radiochemical production at the Mayak Production Association

    Mokrov, Y.; Glagolenko, Y.; Napier, B.

    2000-07-01

    river, rather than relying on a more uncertain reconstruction of quantities released at the point of discharge. Radionuclides considered include {sup 90}Sr, {sup 106}Ru, {sup 137}Cs, and {sup 144}Ce. Estimated concentrations of selected radionuclides at various times are presented.

  18. Reconstruction of radionuclide contamination of the Techa River caused by liquid waste discharge from radiochemical production at the Mayak Production Association.

    Mokrov, Y; Glagolenko, Y; Napier, B

    2000-07-01

    than relying on a more uncertain reconstruction of quantities released at the point of discharge. Radionuclides considered include 90Sr, 106Ru, 137Cs, and 144Ce. Estimated concentrations of selected radionuclides at various times are presented. PMID:10855774

  19. Assessment of doses to biota in the river system

    Doses to aquatic biota in the hydrological system Techa - Ob are estimated.The following water bodies with different levels of radioactive contamination are considered: industrial reservoirs, Techa, Iset, Tobol and Irtysh Rivers. Doses to biota are calculated using the observed data on the content of radionuclides in various environmental components, with consideration for geometric characteristics of the organisms and the exposure sources. The following groups of the river biota are considered: aquatic plants, mollusks and fish. Simplified geometric models (ellipsoids) are used in the internal dose calculations for fish and mollusks. Aquatic plants are approximated either with spheres or with a layer of finite depth. For the external doses assessment the water was considered as an infinite source with the uniform distribution of radionuclides. Sediments were represented as a source with the uniformly distributed activity. Concentration factor of scattered radiation was taken into account for gamma emitters. Sources and levels of radioactive contamination of the Techa - Ob system are analyzed. Data on the activity concentration of radionuclides in water, bottom sediments and aquatic biota are used for the dose assessment. Assessment of doses to biota in the Techa -Ob river system in the period from 1949 to the present time are performed.The highest doses (over 0.01 Gy/day) were received by aquatic organisms in the upper reaches of the Techa River in the period of maximum discharges of radionuclides (1950-1951). In that period, a major contribution to the dose to aquatic organisms was due to the incorporated radionuclides: 89 Sr, 90 Sr, 106 Ru,137 Cs, 144 Ce and others. During 1950-1951, the doses to aquatic organisms were estimated, on average, at 0.003-0.1 Gy/day. After the cessation of intensive radioactive discharges and the construction of a system of protective water bodies, the doses to aquatic biota noticeably decreased. Current levels of exposure to fish in

  20. Solid phase extraction of actinides using polymeric beads impregnated with TODGA

    137Cs is one of the major radionuclides contributing to the activity of the high level waste (HLW) and its separation facilitates the safe disposal of the latter in deep geological repository as vitrified mass. The global inventory of 137Cs was estimated to be around 3.7x1014 kBq in 2010. Due to its long half-life and reasonable gamma energy (661 keV), 137Cs it has potential application as a radiation source in gamma irradiators in the environmental pollution control, food preservation and sterilization of medical accessories. It is, therefore, required to develop efficient separation methods for its recovery from HLW. We have recently reported that solvent system containing calix(4)arene-crown-6 ligands in FS-13 have yielded much improved extraction of radio-cesium as compared to analogous solvent systems containing nitrobenzene as the diluents. Our studies involving four different calix-bis-crown-6 and calix-mono-crown-6 ligands have indicated that calix(4)arene-dibenzo-bis-crown-6 (CBC) ligands were better suited due to more favourable extraction of Cs(I) and radiolytic stability of the ligand. In the present study, we have tried use the developed solvent system for the recovery of radio-cesium (137Cs and 134Cs) from actual high level waste (HLW). The HLW, containing a total activity of 100 Ci/L also contained 3.85 g/L U and 7.09 mg/L Pu which were removed by contacting the waste solution twice with 30% TBP in n-dodecane in a hot-cell facility. The raffinate from the TBP extraction step contained negligible amounts of the actinides and was subsequently contacted four times with 1.0x10-3 M CBC in FS-13 (each time with fresh organic phase) in the hot-cell facility and the extraction results indicated 137Cs to remain in the raffinate out of 15.88 Ci/L suggesting ∼ 97% extraction in 4 stages. Quantitative extraction can be done by increasing the number of stages. It was interesting to note that none of the other radionuclides, such as 144Ce, 106Ru, 95Zr, 95Nb, 90Y

  1. 106Ruthenium Brachytherapy for Retinoblastoma

    Purpose: To evaluate the efficacy of 106Ru plaque brachytherapy for the treatment of retinoblastoma. Methods and Materials: We reviewed a retrospective, noncomparative case series of 39 children with retinoblastoma treated with 106Ru plaques at the Jules-Gonin Eye Hospital between October 1992 and July 2006, with 12 months of follow-up. Results: A total of 63 tumors were treated with 106Ru brachytherapy in 41 eyes. The median patient age was 27 months. 106Ru brachytherapy was the first-line treatment for 3 tumors (4.8%), second-line treatment for 13 (20.6%), and salvage treatment for 47 tumors (74.6%) resistant to other treatment modalities. Overall tumor control was achieved in 73% at 1 year. Tumor recurrence at 12 months was observed in 2 (12.5%) of 16 tumors for which 106Ru brachytherapy was used as the first- or second-line treatment and in 15 (31.9%) of 47 tumors for which 106Ru brachytherapy was used as salvage treatment. Eye retention was achieved in 76% of cases (31 of 41 eyes). Univariate and multivariate analyses revealed no statistically significant risk factors for tumor recurrence. Radiation complications included retinal detachment in 7 (17.1%), proliferative retinopathy in 1 (2.4%), and subcapsular cataract in 4 (9.7%) of 41 eyes. Conclusion: 106Ru brachytherapy is an effective treatment for retinoblastoma, with few secondary complications. Local vitreous seeding can be successfully treated with 106Ru brachytherapy

  2. Influence of variations in dose and dose rates on biological effects of inhaled beta-emitting radionuclides

    The biological effects of inhaled β-emitting radionuclides, 90Y, 91Y, 144Ce and 90Sr, are being investigated in beagle dogs that received single acute exposures at 12 to 14 months of age. The aerosols studied have included 91YC13,144CeC13, 90SrC12, and 90Y, 91Y, 144Ce or 90Sr in aluminosilicate particles. Thus, 91YCl3, 144CeCl3 and the aluminosilicate containing radionuclide particles all resulted in significant exposures to lung; 91YC13, 144CeC13 an 90SrC12 resulted in significant exposures to bone; 91YC13 and 144 CeC13 resulted in significant exposures to liver. The higher initial doserate exposures have been more effective than low dose-rate exposures on a per-rad basis in producing early effects. To date (144CeO2, it was observed that, on a μCi initial lung burden per kilogram body weight basis, mice did not develop pulmonary tumours whereas beagle dogs did. To fid out the reason for this observation mice have been repeatedly exposed by inhalation to 144CeO2 to maintain lung burdens of 144Ce that resulted in radiation dose rates similar to that observed in beagle dogs. Several of the repeatedly exposed mice developed malignant pulmonary tumours. Thus, with similar dose rates and cumulative doses to the lung, mice and dogs responded in a similar manner to chronic β radiation

  3. Separation and recovery of ruthenium from radioactive liquid waste for specific medical applications - wealth from waste

    In recent past, 106Ru has emerged as one of the promising β- emitting radionuclide used in brachytherapy for the treatment of choroidal melanoma and retinoblastoma due to its favorable nuclear decay characteristics. A plaque with low amount of 106Ru activity of the order of 12 - 26 MBq (0.3 - 0.7 mCi ) is suitable for the above treatment and can be used for an adequate duration of 1-2 years due to suitable half-life (T1/2 = 1.02 y). In order to undertake the preparation of 106Ru plaque, an indigenous availability of this radionuclide with acceptable purity was explored from radioactive liquid waste having wide spectrum of fission products in line with wealth from waste strategy. Process methodology has been developed and standardized at Process Control Laboratory of Waste Immobilization Plant (WIP), Trombay for separation of 106Ru from radioactive liquid waste for intended medical application. (author)

  4. Accumulation of transuranic elements in the aquatic biota of the Belarusian sector of contaminated area near the Chernobyl nuclear power plant - Accumulation of transuranic elements in aquatic biota of Belarusian sector of contaminated area of Chernobyl nuclear power plant

    Golubev, Alexander; Mironov, Vladislav [International Sakharov Environmental University. Box 220070, 23 Dolgobrodskaya Street, Minsk, 220070 (Belarus)

    2014-07-01

    The evolution of nuclear contamination of Belarus territory after Chernobyl accident includes the four stages: 1. Iodine-neptunium stage, caused mainly by short-lived radionuclides {sup 131}I, {sup 239}Np and others with a half-life period of several weeks; II. Intermediate stage, caused by radionuclides with a half-life period of a year ({sup 144}Ce, {sup 106}Ru, {sup 134}Cs, etc.); III. Strontium-cesium stage, caused by {sup 90}Sr and {sup 137}Cs with a half-life period of about 30 years; IV. Plutonium-americium, caused by long-lived α-emitting radionuclides {sup 241}Am (period of half-life of 432 years) and {sup 239+240}Pu, having high radio and chemo-toxicity. According to forecasts, activity of {sup 241}Am to 2050 year will increase by 2.5 times and it will be the most important dose-related factor for the aquatic biota within the Chernobyl accident zone. In 2002 - 2008 years we have studied the accumulation of trans-uranic elements (TUE, {sup 241}Am, {sup 239+240}Pu) in basic components of water body ecosystems within the Chernobyl zone - non-flowing Perstok Lake, weak-flowing Borschevka flooding and small Braginka River. Among investigated components are water, bottom sediments, submerged macrophytes (Ceratophyllum submersum, Hydrocharis morsus-ranae, Lemna minor, Nuphar lutea, Stratiotes aloides), emergent macrophytes (Typha spp.), shellfish and fish. In the soil cover in the vicinity of the Perstok Lake activity of {sup 241}Am at present is equivalent to 300 - 600 Bq.kg{sup -1}, that is the basic source of its income to the lake. Radionuclides mobility in the water environment is higher than in the soil, that facilitates the rapid incorporation of {sup 241}Am to the trophic nets of water bodies and its removal by near-water animals in the terrestrial biotopes, including outside Chernobyl zone. Thus, the activity of {sup 241}Am in bottom sediments in the Perstok Lake and Borschevka flooding in 2008 year reach respectively 324 and 131 Bq.kg{sup -1}, and the

  5. Accumulation of transuranic elements in the aquatic biota of the Belarusian sector of contaminated area near the Chernobyl nuclear power plant - Accumulation of transuranic elements in aquatic biota of Belarusian sector of contaminated area of Chernobyl nuclear power plant

    The evolution of nuclear contamination of Belarus territory after Chernobyl accident includes the four stages: 1. Iodine-neptunium stage, caused mainly by short-lived radionuclides 131I, 239Np and others with a half-life period of several weeks; II. Intermediate stage, caused by radionuclides with a half-life period of a year (144Ce, 106Ru, 134Cs, etc.); III. Strontium-cesium stage, caused by 90Sr and 137Cs with a half-life period of about 30 years; IV. Plutonium-americium, caused by long-lived α-emitting radionuclides 241Am (period of half-life of 432 years) and 239+240Pu, having high radio and chemo-toxicity. According to forecasts, activity of 241Am to 2050 year will increase by 2.5 times and it will be the most important dose-related factor for the aquatic biota within the Chernobyl accident zone. In 2002 - 2008 years we have studied the accumulation of trans-uranic elements (TUE, 241Am, 239+240Pu) in basic components of water body ecosystems within the Chernobyl zone - non-flowing Perstok Lake, weak-flowing Borschevka flooding and small Braginka River. Among investigated components are water, bottom sediments, submerged macrophytes (Ceratophyllum submersum, Hydrocharis morsus-ranae, Lemna minor, Nuphar lutea, Stratiotes aloides), emergent macrophytes (Typha spp.), shellfish and fish. In the soil cover in the vicinity of the Perstok Lake activity of 241Am at present is equivalent to 300 - 600 Bq.kg-1, that is the basic source of its income to the lake. Radionuclides mobility in the water environment is higher than in the soil, that facilitates the rapid incorporation of 241Am to the trophic nets of water bodies and its removal by near-water animals in the terrestrial biotopes, including outside Chernobyl zone. Thus, the activity of 241Am in bottom sediments in the Perstok Lake and Borschevka flooding in 2008 year reach respectively 324 and 131 Bq.kg-1, and the activity of 241Am in macrophytes of the Perstok Lake at the same year was 1,0 - 3,7 Bq.kg-1. In

  6. Patterns of Cs-137 and Sr-90 distribution in conjugated landscape systems

    Korobova, E.

    2012-04-01

    The main goal of the study was to reveal spatial patterns of 137Cs and 90Sr distribution in soils and plants of conjugated landscapes and to use 137Cs as a tracer for natural migration and accumulation processes in the environment. The studies were based on presumptions that: 1) the environment consisted of interrelated bio- and geochemical fields of hierarchical structure depending on the level and age of factors responsible for spatial distribution of chemical elements; 2)distribution of technogenic radionuclides in natural landscapes depended upon the location and type of the initial source and radionuclide involvement in natural pathways controlled by the state and mobility of the typomorphic elements and water migration. Case studies were undertaken in areas subjected to contamination after the Chernobyl accident and in the estuary zones of the Yenisey and Pechora rivers. First observations in the Chernobyl remote zone in 1987-1989 demonstrated relation between the dose rate, 137Cs, 134Cs, 144Ce, 106Ru, 125Sb in soil cover and the location of the measured plot in landscape toposequence. Later study of 137Cs and 90Sr concentration and speciation confirmed different patterns of their distribution dependent upon the radioisotope, soil features and vegetation cover corresponding to the local landscape and landuse structure. Certain patterns in distribution and migration of 137Cs and 90Sr in soils and local food chain were followed in private farms situated in different landscape position [1]. Detailed study of 137Cs activity in forested site with a pronounced relief 20 and 25 years after the Chernobyl accident showed its stable polycentric structure in soils, mosses and litter which was sensitive to meso- and micro-relief features [2]. Radionuclide contamination of the lower Yenisey and Pechora studied along meridian landscape transects proved both areas be subjected to global 137Cs pollution while the Yenisey floodplain received additional regional contamination

  7. Langzeitergebnisse bei Aderhautmelanom nach 106Ruthenium-Brachytherapie

    Krause, Nona

    2015-01-01

    Introduction: 106Ruthenium-brachytherapy (106Ru-brachytherapy) is an established therapy for small and medium-sized uveal melanomas. The aim of this study was to examine the long-time results in regard to recurrence rate, complication rate, ocular preservation, metastasis rate and survival with malignant uveal and ciliary body melanoma, as well as relevant prognosis factors, subsequent to 106Ru-brachytherapy. Methodology: In this retrospective study of all cases with uveal or with ciliary ...

  8. Nasal carcinomas in beagle dogs after inhalatioon of relatively soluble forms of beta-emitting radionuclides

    Beagle dogs were exposed by inhalation to relatively soluble forms of three beta-emitting radionuclides and are being held for life span observation to evaluate hazards associated with nuclear power production. Dogs were exposed to graded activity levels of 91YCl3, 144CeCl3 or 90SrCl2. With 91YCl3 and 144CeCl3, significant radiation dose was delivered to liver, respiratory tract, and skeleton. With 90SrCl2, the dose was essentially to skeleton. Nasal cavity squamous cell carcinomas have been the most frequent neoplasms in the 91Y and one of the most frequent in the 144Ce study while relatively few have been seen after 90Sr exposure. Also one nasal cavity hemangiosarcoma was seen in the 144Ce study. The 90Sr-exposed dogs have survived longer after exposure and have higher skeletal radiation doses than do the dogs exposed to 91Y or 144Ce. The greater incidence of nasal carcinomas can be explained by the finding of high concentrations of the lanthanides, 91Y and 144Ce, associated with the nasal turbinate epithelium

  9. Effects of the purification techniques applied to industrial wastes on the chemical behaviour of ruthenium 106 in the marine environment. The case of La Hague reprocessing plant releases

    Since nuclear fuel reprocessing started at the La Hague plant in 1966, the efficiency of the purification techniques applied to radioactive wastes has been improved by a factor of 600. The chemical behaviour of 106Ru observed in the liquid releases into the sea and at two coastal sites near the outlet, shows time variations related to the evolution of the reprocessing techniques used. The ''wet chemical method'' based on 106Ru coprecipitation with cobalt sulphide has fulfilled the objectives of environmental protection and the requirements of industrial productivity. As a consequence, 106Ru behaves like the weakly reactive complexes formed during the nitric acid dissolution stage of the process. Since 1989, vitrification of the effluents mainly affected by these complexes and the optimization of the wet method have contributed to the reduction of 106Ru liquid releases into the sea. At the same time, the radionuclide chemical non-reactivity has been attenuated. Measurements of 106Ru activity carried out in the seaweed Fucus serratus show that the availability of nitrosylruthenium in seawater is closely related to hydrolysis of the complexes. Hydrolysis products are the main source of the chemical species available for exchange with the seaweed, its concentration factor being estimated at 500 ± 350. (authors). 26 refs., 10 tabs., 6 figs

  10. Validity of chalk and bentonite application in soil and water on reducing the absorption of ratio-strontium and radio-cerium by crop

    Effects of the chalk and bentonite application in soil and surface water respectively on reducing the absorption of 89Sr and 141Ce by crop (especially in the edible part of crop) were studied by using isotope tracer techniques. The results showed that the specific activity of 89Sr in the ryegrass and Chinese cabbage could be decreased significantly by chalk application in the soil. The reduced ratio of 89Sr absorption of Chinese cabbage and ryegrass reached 77.7% and 35.2% respectively with the chalk application of 20 g/kg soil. The specific activity of 89Sr in ryegrass and Chinese cabbage followed obvious negative linear correlation with the quantity of application chalk in the soil. The specific activity of 141Ce in surface water, chaff and brown rice decreased by application bentonite in the surface water, which led to the lower accumulation of 141Ce in paddy. However, the absorption and accumulation of 141Ce in root and straw could not be changed. The specific activity of 141Ce in soil followed a negative exponential relation with depth of soil profile

  11. Genetic effects induced by radionuclides in the populations of the chlorella and antimutagenic influence of the vitamins C and B12

    Genetic influence of 90Sr, 137Cs and 144Ce on the chlorella populations has been studied, as well as antimutagenic effect of C and B12 vitamins on the influenced by 90Sr and 144Ce chlorella populations. The radionuclides 90Sr, 137Cs and 144Ce have been determined to increase the number of lethal and mutant cells in the chlorella populations. It has been shown that according to the influence of the number of lethally injured cells the radionuclides under study (within the concentration range 3.7X104 - 3.7X106 Bk/l) may be presented by the sequence 144Ce>137Cs≥90Sr, while according to the influence of the number of mutant cells - by the reverse sequence 90Sr>137Cs≥144Ce. Such different effect of the radionuclides on the chlorella populations may, possibly, be explained by different physical-chemical state of these radionuclides in water medium, their different uptake mechanism in plant cells, and different localization in them. A conclusion is drawn that C and B12 vitamins reduce radiosensitivity of water organisms, especially their lethality. B12 vitamin is stornger a mutagen than vitamin C

  12. Elimination of cerium-144 - physical and biological characteristics

    The decontamination efficiency of the preparation pentacyn (CaNa3-DTPA) with regard to radiocerium was evaluated. Investigated were not only physical parameters (radionuclide kinetics, absorbed doses decrease), but also morphological and biochemical indexes. Four groups of male Wistar rats were treated accordingly with 144Ce; 144Ce + pentacyn; external irrradiation + 144Ce; external irradiation + 144Ce + pentacyn. External gamma irradiation was performed with a dose of 260 cGy, 144Ce (1480 kBq/animal) was introduced intratarcheally 1 h after external irradiation. Pentacyn was administred according to the following scheme, ensuring maximal efficiency and minimal toxicity: intratracheally administration 30 min after radionuclide intake by 0.2 ml and subsequent intraperitoneally applications on days 1, 3, 5, 7, 10 and 17 by 0.5 ml. Determined were the following parameters characterizing the development of fibrous process: the quantity of oxyproline in collagen, the quantity of hexosamine in lung tissues, the changes in dry mass and heart camera index. It was concluded that biological criteria are important component of the decontamination efficiency evaluation

  13. Physiological and genetic effects induced in the chlorella culture by radionuclides

    Radionulcides 90Sr. 137Cs and 144Ce suppress chlorella populations in 37-10-6-37X10-4 Bk/e copcentration range; they increase the amount of lethally damaged and mutant cells at that. Investigated radionuclides can be presented in the form of 144Ce > 137Cs > 90Sr series with respect to their effect on the intensity of chlorella population photosynthesis and amount of lethally damaged cells. as well as accumulation levels, and in the form of 90Sr 137Ce > 144Ce series with negative sequence with respect to the effect on cell density, especially on the amount of mutant cells. The inverse relationship betWeen the change of photosynthesis intensity and the amount of lethally damaged cells, as well as betWeen the change of cell density and the maount of mutant cells was observed during radionuclide effect on chlorella populations

  14. Combinative effect of medium physical and chemical factors on the penetration and localization of some radionuclides in water plant cells

    As a result of the experiments, carried out with the charophytes algae Nitellopsis obtusa, gathered from lake Drukshyaj (the North-East part of the Lithuanian SSR) in 1985, it has been determined that the 90Sr, 144Ce and 137Cs radionuclides accumulation by water plant cell constituents (wall, protoplasm, vacuole) is substantially influenced by the water temperature, the chemical substances, which change the water structure, as well as the combinative effect of these factors. An identical character of the changes of the accumulation factors of 90Sr and 137Cs, which are found in the water solutions in an ionic form, and slightly different character in the case of 144Ce, which exists by 85% in the form of colloid particles, have been noted. In the case of 144Ce the influence of the physical as well as chamical factors on the cell walls is felt stronger than on the inner cell membranes

  15. In situ responses of a biological indicator Mytilus edulis L. to the variations of radionuclide discharges from a fuel reprocessing plant

    The introduction of 10 lots of 100kg of mussels in La Hague waters made it possible to investigate the in situ uptake kinetics of 106Ru + 106Rh released by the fuel reprocessing plant of La Hague during 1 year. Equilibrium was reached within 1 - 3 months, whatever the time of introduction and the amounts released. The removal of the mussels labelled at La Hague to a remote aera made it possible to calculate the biological half-life of 106Ru + 106Rh, viz from 16 to 18 days

  16. Assessment of a cerium---praseodymium-144 inhalation case

    A case involving an acute exposure to a 144Ce-144Pr contaminated atmosphere is presented with a discussion of the treatment and evaluation of data collected out to 800 days post intake. Treatment included irrigation of the upper nasal passages with normal saline, nebulization with normal saline mist and DTPA therapy. Assessment of the deposition and the resulting dose commitment was based on in vivo measurements and excretion data. The initial pulmonary burden, which cleared with three distinct half times, was estimated at 2.1 μCi of 144Ce

  17. Assessment of a cerium-praseodymium-144 inhalation case

    A case involving an acute exposure to a 144Ce-144Pr-contaminated atmosphere is presented with a discussion of the treatment and evaluation of data collected up to 800 days post-intake. Treatment included irrigation of the upper nasal passages with normal saline, nebulization with normal saline mist, and intravenous DTPA therapy. Assessment of the deposition and the resulting dose commitment was based on in vivo measurements and excretion data. The initial pulmonary burden, which cleared with three distinct half-times, was estimated at 2.1 μCi of 144Ce. (author)

  18. Separation of radioactive substances by anodic electrolysis

    In experiments on the electrodeposition of radioisotopes on a platinum anode it was observed that the isotopes could be classified into: (1) those whose cations are deposited as oxides; and (2) those whose cations are only adsorbed on the anode. Under given conditions this difference can be used to separate ions of the two groups. In the present paper, experimental details are given of the separation of 144Ce from 140La. The separation of 144Ce from uranium fission products in the presence of uranyl ion is also discussed. (U.K.)

  19. Toxicity studies of inhaled beta-emitting radionuclides: status report

    The influence of total dose and dose rate on the effects of inhaled beta-emitting radionuclides is being studied in laboratory animals. The radionuclides are inhaled either in a relatively soluble form (90SrCl2, 144CeCl3, 91YCl3 or 137CsCl) or in a relatively insoluble form in fused aluminosilicate particles. The organs affected depend on the solubility and chemical characteristics of the radio isotopes. Studies with young adult dogs are complemented with comparable studies in other species (mice, rats and Syrian hamsters), with animals of different ages and with animals repeatedly exposed to 144Ce

  20. Toxicity studies of inhaled beta-emitting radionuclides - status report

    The influence of total dose and dose rate pattern on the effects of inhaled β-emitting radionuclides is being studied in laboratory animals. The inhaled radionuclides were either in a relatively soluble form (90SrCl2, 144CeCl3, 91YCl3, or 137CsCl), or in a relatively insoluble form in fused aluminosilicate particles. The organs affected depend on the solubility and chemical characteristics of the radionuclides. Studies with young adult dogs are complemented by comparable studies in other species (mice, rats, and Syrian hamsters), with animals of different ages and animals repeatedly exposed to 144Ce. 12 references, 2 figures, 2 tables

  1. Influences of marine sediment on the accumulation of radionuclides by green alga (Ulva pertusa)

    Distribution of radionuclides (60Co, 137Cs, 95Zr-95Nb and 106Ru-106Rh) among green alga (Ulva pertusa), sea water and marine sediment were examined by radioisotope tracer experiment in order to estimate the influence of sediment on the accumulation of radionuclides by the alga. By the application of the compartment model to the experimental results, exponential formulas of distributions were obtained. Through comparison of the transfer coefficients of radionuclides calculated from the exponential formulas, the influence of the sediment on the accumulation of the radionuclides by the green alga was determined to be the largest for 60Co, followed by 95Zr-95Nb, 106Ru-106Rh and 137Cs in this order. The activity ratios of 95Zr-95Nb and 106Ru-106Rh calculated from the transfer coefficients are larger for the alga than for the sediment, inversely those of 60Co and 137Cs show higher values for the sediment than for the alga. Especially, in the case of 60Co, the activity ratio for the sediment is approximately 20 times greater than that for the alga. Biological half lives in green alga estimated from the transfer coefficients were 10 days for 60Co, 7 days for 137Cs, 26 days for 95Zr-95Nb and 24 days for 106Ru-106Rh. (auth.)

  2. Impacts in groundwater of effluents arising in the nuclear industry

    The following topics are discussed: modes of entry of radioactive wastes into groundwater; movement of radionuclides in the ground; degradation processes; behavior of tritium, 90Sr, 137Cs, 106Ru and transuranic elements; potential pathways to man; and impact of releases of radioactive materials to the ground compared to radiation protection standards. (U.S.)

  3. Comparison of influences of sediments and sea water on accumulation of radionuclides by worms

    The accumulation and excretion of radionuclides by marine polychaete worms (Nereis japonica) were examined to learn the influence of contaminated sediments on the contamination of marine organisms. The concentration factors of 60Co, 95Zr-95Nb, 106Ru-106Rh and 137Cs for unfed worms were 6, 4, 6 and 6 respectively, and they were similar to the concentration factors for unfed worms. The biological half lives of 60Co, 95Zr-95Nb and 106Ru-106Rh for fed worms were similar to each other (37, 32 and 35 days, respectively) except that of 137Cs (6 days), and all of them were a little shorter than those for unfed worms. The transfer ratios of radionuclides from sediments to worms were 5 per cent for 60Co, 0.9 for 95Zr-95Nb, 0.6 for 106Ru-106Rh and 17.9 for 137Cs in cpm/g in regard to initial activity in sediments. These figures were compared with the concentration factors to estimate the influence of sediments on the contamination of marine organisms. The obtained figures, which we call the biological factor of the sediments, were 120, 440, 1000 and 30 for 60Co, 95Zr-95Nb, 106Ru-106Rh and 137Cs, respectively. (auth.)

  4. The relationship between revascularisation and osteogenesis in fresh or demineralised bone grafts

    Solheim, E; Pinholt, E M; Talsnes, O;

    2001-01-01

    Bone formation generally depends on adequate blood flow. Failure of bone grafts has been attributed to delayed revascularisation of the graft. We compared the relationship between revascularisation and osteogenesis, evaluated as entrapment of (141)Ce-labelled microspheres and uptake of (85)Sr, re...

  5. Revascularisation of fresh compared with demineralised bone grafts in rats

    Solheim, E; Pinholt, E M; Talsnes, O;

    2001-01-01

    Revascularisation of bone grafts is influenced by both the anatomical origin and the pre-implantation processing of the graft. We investigated the revascularisation by entrapment of 141Ce (cerium)-labelled microspheres in large, fresh and demineralised syngeneic grafts of predominantly cancellous...

  6. Separation of cerium from high level waste solution of Purex origin

    A simple solvent extraction procedure for the separation of 144Ce from Purex high level waste (HLW) is described. 2-ethylhexyl 2-ethylhexyl phosphonic acid (KSM-17) has been used as extractant. About 10 mCi of cerium was separated from HLW using this technique. This method is amenable for automation and scale up. (author)

  7. Comparison of the effects of inhaled alpha- and beta-emitting radionuclides on pulmonary function in the dog

    Alterations of pulmonary function in representative groups of dogs developing nonneoplastic lung disease, after single inhalation exposures to cerium-144 or plutonium-238 in relatively insoluble particulate forms, were compared. The inhaled particles had similar aerodynamic diameters and effective half-lives of retention in the lung. The mean initial lung burdens of the 144Ce- and 238Pu-exposed groups were 51 and 0.65 μCi/kg of body weight, respectively. Because of the respective ranges of the beta emissions from 144Ce and the alpha emissions from 238Pu, the lungs of the 144Ce-exposed dogs were relatively uniformly irradiated, whereas only approximately 6% of the lung tissue of rates to the 238Pu-exposed dogs was irradiated. The calculated average dose rates to the irradiated tissue were similar for both radionuclides. Pulmonary function was measured serially without sedation. Both groups developed progressive, restrictive lung disease, which ended in death from pulmonary failure. Dogs that inhaled 144Ce had an early reduction of CO diffusing capacity followed by a progressive mechanical and gas-exchange impairment similar to that reported for dogs and men exposed to external irradiation. Dogs that inhaled 238Pu had increased respiratory frequencies which often persisted for months before mechanical and gas-exchange abnormalities became evident

  8. Radiation-induced liver lesions in beagle dogs

    The risk for liver disease from internally deposited beta-emitting radionuclides is unknown because there are no human populations exposed to hepatotropic beta-emitting radionuclides available for study. In this report, we discuss the hepatic lesion in dogs exposed to a beta-emitting radionuclide, 144CeCl3, and held for their life spans

  9. Calculation of beta-ray dose distributions from ophthalmic applicators and comparison with measurements in a model eye

    Dose distributions throughout the eye, from three types of beta-ray ophthalmic applicators, were calculated using the EGS4, ACCEPT 3.0, and other Monte Carlo codes. The applicators were those for which doses were measured in a recent international intercomparison [Med. Phys. 28, 1373 (2001)], planar applicators of 106Ru-106Rh and 90Sr-90Y and a concave 106Ru-106Rh applicator. The main purpose was to compare the results of the various codes with average experimental values. For the planar applicators, calculated and measured doses on the source axis agreed within the experimental errors (106Ru-106Rh and 5 mm for 90Sr-90Y. At greater distances the measured values are larger than those calculated. For the concave 106Ru-106Rh applicator, there was poor agreement among available calculations and only those calculated by ACCEPT 3.0 agreed with measured values. In the past, attempts have been made to derive such dose distributions simply, by integrating the appropriate point-source dose function over the source. Here, we investigated the accuracy of this procedure for encapsulated sources, by comparing such results with values calculated by Monte Carlo. An attempt was made to allow for the effects of the silver source window but no corrections were made for scattering from the source backing. In these circumstances, at 6 mm depth, the difference in the results of the two calculations was 14%-18% for a planar 106Ru-106Rh applicator and up to 30% for the concave applicator. It becomes worse at greater depths. These errors are probably caused mainly by differences between the spectrum of beta particles transmitted by the silver window and those transmitted by a thickness of water having the same attenuation properties

  10. Application of multiple gamma-ray spectrum for analytical chemistry

    Hatsukawa, Yuichi; Hayakawa, Takehito; Shinohara, Noboru; Oshima, Masumi [Japan Atomic Energy Research Inst., Tokai, Ibaraki (Japan). Tokai Research Establishment

    2000-01-01

    Feasibility of application of the multi-gamma ray spectrum for analytical chemistry was examined. A specimen in which some minor fission products are included was measured at an array of ten germanium detectors with BGO Compton suppressors, GEMINI, and multiple gamma-ray spectra are measured. Even in very strong radiation fields from {sup 137}Cs isotope, some miner contents, {sup 106}Ru, {sup 125}Sb, {sup 144}Pr, {sup 207}Bi were detected by this method. (author)

  11. 2. Quarterly progress report, 1983

    This quarterly report of the SCPRI exposes an interpretation of the principal results concerning the surveillance of radioactivity in the environment: atmospheric dusts, rainwater, surface water, underground water, irrigation water, drinking water, food chain, sea water around nuclear plant sites and other sites. The activities of various radioisotopes are presented in tables (7Be, 58Co, 60Co, 134Cs, 137Cs, 90Sr, 106Ru, K, 54Mn, U and T). A bibliographic selection is also presented

  12. 3. Quarterly progress report 1982

    This quarterly report of the SCPRI exposes an interpretation of the principal results concerning the surveillance of radioactivity in the environment: atmospheric dusts, rainwater, surface water, underground water, irrigation water, drinking water, food chain, sea water around nuclear plant sites and other sites. The activities of various radioisotopes are presented in tables (7Be, 58Co, 60Co 134Cs, 137Cs, 90Sr, 106Ru, K, 54Mn, U and T). A bibliographic selection is also presented

  13. 4. Quarterly progress report, 1982

    This quarterly report of the SCPRI exposes an interpretation of the principal results concerning the surveillance of radioactivity in the environment: atmospheric dusts, rainwater, surface water, underground water, irrigation water, drinking water, food chain, sea water around nuclear plant sites and other sites. The activities of various radioisotopes are presented in tables (7Be, 58Co, 60Co, 134Cs, 137Cs, 125Sb, 90Sr, 106Ru, K, 54Mn, U and T). A bibliographic selection is also presented

  14. Separation of valuable fission products from High Level Liquid Waste (HLLW)

    High Level Liquid Waste (HLLW) generated during spent fuel reprocessing (PUREX) is an important source of valuable fission products viz. 137Cs, 90Sr (and its daughter product 90Y), platinum group metals like 106Ru , Pd etc. We present a short overview of the work carried out in our laboratory on the separation of the valuable radionuclides from actual research reactor HLLW employing a host of separation techniques like solvent extraction, precipitation, liquid membrane etc. (author)

  15. Partitions of 4d Transition Metal Nuclei and Related Correlations Using the Core Cluster Model

    Mageed, K E Abd El

    2013-01-01

    In the present work we attempt to study the cluster model in the transition metal region. The spectrum fitting method is studied for the selected nuclei (88,90,92^Sr, 92,94^Zr, 98,100^Mo, 100,102,104, 106^Ru, 108,110^Pd and 112,114,116,118^Cd) with proton number (38 0+), the excitation energies and the product of valence nucleon numbers of the parent nuclei.

  16. 1. Quaterly progress report, 1980

    This quaterly report of the SCPRI exposes an interpretation of the principal results concerning the surveillance of radioactivity in the environment: atmospheric dusts, rainwater, surface water, underground water, irrigation water, drinking water, food chain, sea water around nuclear plant sites and other sites. The activities of various radioisotopes are in tables (7Be, 131I, 137Cs, 90Sr, 106Ru and 106Rh, 226Ra, 54Mn, U and T). A bibliographic selection is also presented

  17. Preparation of ruthenium nitrosyl nitrate solutions and the extraction of ruthenium complexes by means of neutral organic phosphorus compounds

    A method is described for the preparation of solutions of nitrosyl nitrate complexes of ruthenium. Ruthenium chloride has been transformed into ruthenium tetroxide which reacted with nitrogen oxides in nitric acid and formed ruthenium nitrosyl nitrate. The solution has been labelled with 106Ru and spectrophotometrically investigated. The extraction behavior of the ruthenium complexes with neutral organic phosphorous compounds has been investigated as a function of the acid and salt concentration of the solution and compared with that of other fission products. (author)

  18. Acute toxicity of beta-emitting radionuclides that may be released in a reactor accident and ingested

    Suckling, weanling, and adult rats received 106Ru--106Rh by gavage and adult beagle dogs ingested 106Ru--106Rh to determine the toxicity of this high-energy (1.4 MeV av) β-emitting nuclide pair. The LD50's for suckling, weanling, and adult rats were 1.5, 18, and 9.0 mCi/kg, respectively. Adult rats were given 147Pm by gavage to determine if a low-energy (0.06 MeV av) β emitter could also cause death by damaging the bowel. The LD50 of 147Pm in rats was about 5 Ci/kg. The calculated radiation doses absorbed in the target cells at the LD50 level were approximately the same for the two radionuclides (3500 rad), although the doses at the mucosal surface differed widely. The LD50 for 106Ru--106Rh in dogs was about 3.5 mCi/kg. Dosimeters placed beneath the mucosa in dogs indicated that the radiation dose to the target cells that caused death from 106Ru--106Rh was about the same as it was for rats. The signs of intestinal injury, their duration, and the probabilities of tissue repair were much different in the dog than in the rat. The midcolon and lower colon of dogs were usually denuded at focal sites after ingestion of 2.5 to 4.0 mCi/kg, and frequently that damage was irreversible. The fatal consequence of severe mucosal damage was averted in two dogs by colectomy and an ileorectal anastomosis

  19. Effect of tropicamide on ocular blood flow in the rabbit

    Intracardiac injection of 15 microspheres labeled with 85Sr (strontium) and 141Ce (cerium) were used to determine ocular blood flow in seven rabbits before and 25 min after bilateral application of tropicamide to the cornea. By using two different isotopes distinguishable under gammaspectrometry, each animal served as its own control. After administration of two drops of 1% tropicamide, no significant difference in blood flow between treated and untreated eyes was observed

  20. Decontamination of a radioactive process waste water by adsorbing colloid flotation

    As a part of a research programme on the treatment of a radioactive process waste water by foam separation techniques, adsorbing colloid flotation was tested to remove 144Ce, 60Co, 65Zn and 89Sr from the waste water. Potassium oleate was used as the collector, and Fe(III) hydroxide, Al(III) hydroxide or Co(II) hydroxide as the coprecipitant. Under the optimal conditions; removals exceeding 99% could be achieved for 65Zn with any of the tested coprecipitants, for 144Ce with Fe(III) and Co(II) hydroxides and for 60Co with only Co(II) hydroxide. For 89Sr removals > 90% could be achieved with only Fe(III) hydroxide. The adsorbing colloid flotation process was compared with both chemical precipitation and ion exchange, and advantages of adsorbing colloid flotation were enumerated. (author)

  1. Decontamination of radioactive process waste water by adsorbing colloid flotation

    Adsorbing colloid flotation was tested to remove 144Ce, 60Co, 65Zn, and 89Sr from radioactive process waste water. Potassium oleate was used as the collector, and Fe(III) hydroxide, Al(III) hydroxide or Co(II) hydroxide as the coprecipitant. Under optimal conditions, removals exceeding 99% could be achieved for 65Zn with any of the tested coprecipitants, for 144Ce with Fe(III) and Co(II) hydroxides and for 60Co with only Co(II) hydroxide. For 89Sr removals of 90% could be achieved only with Fe(III) hydroxide. The adsorbing colloid flotation process was compared with both chemical precipitation and ion exchange. Advantages of adsorbing colloid flotation are discussed. (author)

  2. Combining of some trace elements with constituent materials of marine algae

    Two radionuclides (137Cs and 106Ru-106Rh) were extracted from a brown alg a (Eisenta bicyclis) into 5 solvents (Ethyl ethel, 80% Ethyl alcohol, boiled water, 0.2% NaOH and 24% KOH) in different proportions, suggesting that both radionuclides do not combine with fats and pigments, and that 137Cs associates maybe with dextrans and monosaccharides, while, 106Ru-106Rh mainly combines with the cell wall polysaccharides such as alginic acid and fucoidan. In order to obtain information from extracts of algae, gel filtration was carried out on 2 species of algae (Ulva pertusa and Eisenia bicyclis) using Sephadex G-100 and G-25. Gel filtration profile gave only one peak for 137Cs, 2 for 106Ru-106Rh and 125I, and 3 for 60Co corresponding to positions where saccharides of the algae appeared. As the result, it was found that different radionuclides combined with different constituent materials of an alga, to some extent. Gel filtration profiles of 125I were compared with each other among several species of marine algae. They were different from one another among classes of green, brown and red algae, though they were similar in a class. Gel filtration profiles of 125I were also varied between 2 chemical forms of 125I (Na125I and Na125IO3). (J.P.N.)

  3. Placental transfer of ruthenium in rat and guinea-pig

    Ruthenium-106 in citrate solution was administered intravenously to rat at different stages of pregnancy and to guinea-pig either before conception or in late pregnancy. The results for rat showed that retention in the embryo/foetus measured at 3-5 days after administration increased from about 0.0002% of injected activity per embryo/foetus on day 12 of gestation to about 0.05% at birth. The relative concentrations of 106Ru in embryo/foetus and mother (Cf/Cm ratio) were about 0.1 in each case. Concentrations in the yolk sac on day 12 were about 1% g-1 compared with 0.01% g-1 kin the foetus/ Retention in the guinea-pig foetus in late gestation at 7 days after administration (days 50-57) was about 0.2% injected activity per foetus, corresponding to a Cf/Cm = 0.2. Retention in each foetoplacental unit was 2% of injected 106Ru with 50% in the yolk sac, 35% in the placenta and 10% in the foetus. For administration 4 weeks prior to conception, the level of 106Ru retained in the foetus on day 57 of gestation was two orders of magnitude lower than after short-term administration, with a Cf/Cm about 0.004. (author)

  4. Development of A phantom for ophthalmic beta source applicator quality control using TL dosimetry

    Barbosa, N. A.; da Rosa, L. A. R.; Braz, D.

    2015-11-01

    Concave eye applicators with 90Sr/90Y and 106Ru/106Rh beta ray sources are usually used in brachytherapy for the treatment of superficial intraocular tumors as uveal melanoma with thickness up to 5 mm. The calculation of the dose delivered to the eye is carried out based on the data present in the beta source calibration certificate. Therefore, it would be interesting to have a system that could evaluate that dose. In this work, an eye phantom to be used with 106Ru/106Rh betatherapy applicators was developed in solid water. This phantom can hold nine micro-cube thermoluminescent (TL) dosimeters, TLD-100. The characteristics of the TL response of the dosimeters, namely reproducibility and individual sensitivity, were determined for a 60Co source. Using Monte Carlo code MCNPX, the dose to a water eye was determined at different depths. Exposing the eye phantom with TL dosimeters to the 106Ru/106Rh applicator, it is possible to assess calibration factors using the dose values obtained by Monte Carlo simulation to each depth. Using mean calibration factors, dose values obtained by TL dosimetry were compared to the data present in the applicators certificate. Mean differences for both applicators were lower than ±10%, maximum value 17% and minimum value 0.08%. Considering that the certificate values present an uncertainty of ±20%, the calibration procedure and the developed phantom are validated and can be applied.

  5. Accumulation and excretion of radionuclides by alga Chara tomentosa

    It has been found in the course of the study of accumulation and excretion of radionuclides by alga chara tomentosa that 55Fe, 60Co, 91Y are accumulated by living and dead components of alga chara tomentosa to a far greater extent and are stronger retained than 90Sr, 137Cs, 144Ce. The main part of the absorbed quantities of all investigated nuclides (80-92%) is fixed on the surface of the plant in the ''cortex'' layer

  6. Radio-isotope converter

    Due to the surface power density required for thermoelectric and thermionic converters, available radioactive sources are surveyed and listed. Curves of specific minimum diameter versus thermal flux density are given. 210Po and 242Cm appear to be suitable for direct thermionic when alpha emitters such as 238Pu and 244Cm are still suitable for thermoelectric conversion. This mode will also work with beta emitters 170Tm, 90Sr, 144Ce and 137Cs. Some thermoelectric radioisotope heated converters are suggested. (authors)

  7. Electrochemical investigation of rare earth amalgams

    Using the method of filtration of heterogeneous samarium amalgams, containing radioactive isotopes sup(144)Ce and sup(152)Eu, it has been shown that cerium is inserted into the solid phase of samarium amalgam, whereas europium does not cocrystallize with samarium. The solubility of praseodymium, neodymium, and gadolinium in mercury has been determined on the basis of the curves current VS time of decomposition of heterogeneous amalgams of these metals

  8. High voltage deposition of daughter 144Pr on platinum electrode from chlorbenzene solution of cerium 8-hydroxyquinolinate

    The deposition of 144Pr, carrier-free, on platinum electrode, formed by beta-decay of 144Ce which was in the form of cerium tetrakis (8-hydroxyquinolinate) chelate in chlorobenzene, was studied in dependence on time and intensity of the electric field. The amount of 144Pr deposited on the cathode after 20 min at the intensity of electric field 8 kV cm-1 was 14% of its total equilibrium amount in the solution. The proportion of 144Pr formed in the solution as ions was found by extrapolating the experimental relationships to be 23%. This value was similar to that of the break-up of molecular forms under the formation of simple 144Pr ions expected on the basis of the decay scheme of 144Ce and the mechanism of the energy transfer inside the atoms and molecular systems. On the basis of the mobility of cations found (9.6x10-5 cm2kV-1s-1) it was assumed that deposited ions were probably monotypes. The amount of 144Pr deposited on the anode was about 1% and that of 144Ce on both the cathode and the anode (caused by adsorption) was 0.5 to 1%. (author)

  9. Comparison of the effects of inhaled alpha- and beta-emitting radionuclides on pulmonary function of the dog

    Pulmonary function changes of representative dogs after inhalation of a relatively insoluble form of 144Ce in fused aluminosilicate particles and 238PuO2 were compared. Both radionuclide forms had approximately the same effective half-life, but the 238PuO2 irradiated 11 percent of the lung while the 144Ce irradiated 100 percent. Both groups developed restrictive lung disease progressing to pulmonary failure but the sequence of functional changes differed. The first change in dogs that inhaled 144Ce was a reduced CO diffusing capacity followed later by changes in breathing pattern, lung compliance and alveolar-capillary O2 exchange. The first change in dogs that inhaled 238PuO2 was an increase in respiratory frequency which persisted for several months before nearly simultaneous changes in diffusing capacity, compliance and gas mixing. An impairment in alveolar-capillary O2 exchange occurred later in dogs that inhaled 238PuO2. Functional alterations of both groups in pulmonary failure were similar. The differences in the pattern of functional changes were thought to be related to differences in dose pattern, but the exact relationships are unknown

  10. Pulmonary carcinogenesis and chronic beta irradiation of lung

    Light water nuclear power reactor fuel cycles at various stages contain substantial quantities of β-emitting radionuclides. Thus, in the event of an accident, there is potential for inhalation exposure of man to various types and forms of β-emitting radionuclides. In order to study the biological effects of such potential exposures, a series of life span studies have been initiated in which beagle dogs have been exposed to inhalation to achieve graded lung burdens of a relatively insoluble fused clay form of β-emitting radionuclides. The specific radionuclides, 90Y, 91Y, 144Ce, or 90Sr, were selected on the basis of physical half-life to produce a variety of radiation-dose patterns to the lung. Early effects have been the development of radiation pneumonitis and progressive pulmonary fibrosis. In general, dogs which receive high- and rapidly-declining dose-rate exposure from 90Y or 91Y die earlier and at lower cumulative doses than dogs exposed to 144Ce or 90Sr. By contrast, the incidence of later-occurring malignant lung tumors and the degree of inflammatory response is greater in dogs which received protracted low dose-rate exposure associated with 144Ce and 90Sr. Of particular note is the nature of the lung tumors thus far observed

  11. Brachytherapy treatment simulation of strontium-90 and ruthenium-106 plaques on small size posterior uveal melanoma using MCNPX code

    Abstracts: Concave eye applicators with 90Sr/90Y and 106Ru/106Rh beta-ray sources are usually used in brachytherapy for the treatment of superficial intraocular tumors as uveal melanoma with thickness up to 5 mm. The aim of this work consisted in using the Monte Carlo code MCNPX to calculate the 3D dose distribution on a mathematical model of the human eye, considering 90Sr/90Y and 160Ru/160Rh beta-ray eye applicators, in order to treat a posterior uveal melanoma with a thickness 3.8 mm from the choroid surface. Mathematical models were developed for the two ophthalmic applicators, CGD produced by BEBIG Company and SIA.6 produced by the Amersham Company, with activities 1 mCi and 4.23 mCi respectively. They have a concave form. These applicators' mathematical models were attached to the eye model and the dose distributions were calculated using the MCNPX ⁎F8 tally. The average doses rates were determined in all regions of the eye model. The *F8 tally results showed that the deposited energy due to the applicator with the radionuclide 106Ru/106Rh is higher in all eye regions, including tumor. However the average dose rate in the tumor region is higher for the applicator with 90Sr/90Y, due to its high activity. Due to the dosimetric characteristics of these applicators, the PDD value for 3 mm water is 73% for the 106Ru/106Rh applicator and 60% for 90Sr/90Y applicator. For a better choice of the applicator type and radionuclide it is important to know the thickness of the tumor and its location. - Highlights: ► 106Ru and 90Sr β applicators were modeled using Monte Carlo code MCNPX. ► Dose distributions were calculated for all eye structures, including a tumor region. ► 106Ru generates higher lens doses than those generated by 90Sr

  12. Brachytherapy treatment simulation of strontium-90 and ruthenium-106 plaques on small size posterior uveal melanoma using MCNPX code

    Barbosa, N. A.; da Rosa, L. A. R.; Facure, A.; Braz, D.

    2014-02-01

    Concave eye applicators with 90Sr/90Y and 106Ru/106Rh beta-ray sources are usually used in brachytherapy for the treatment of superficial intraocular tumors as uveal melanoma with thickness up to 5 mm. The aim of this work consisted in using the Monte Carlo code MCNPX to calculate the 3D dose distribution on a mathematical model of the human eye, considering 90Sr/90Y and 160Ru/160Rh beta-ray eye applicators, in order to treat a posterior uveal melanoma with a thickness 3.8 mm from the choroid surface. Mathematical models were developed for the two ophthalmic applicators, CGD produced by BEBIG Company and SIA.6 produced by the Amersham Company, with activities 1 mCi and 4.23 mCi respectively. They have a concave form. These applicators' mathematical models were attached to the eye model and the dose distributions were calculated using the MCNPX *F8 tally. The average doses rates were determined in all regions of the eye model. The *F8 tally results showed that the deposited energy due to the applicator with the radionuclide 106Ru/106Rh is higher in all eye regions, including tumor. However the average dose rate in the tumor region is higher for the applicator with 90Sr/90Y, due to its high activity. Due to the dosimetric characteristics of these applicators, the PDD value for 3 mm water is 73% for the 106Ru/106Rh applicator and 60% for 90Sr/90Y applicator. For a better choice of the applicator type and radionuclide it is important to know the thickness of the tumor and its location.

  13. Deposition of long-lived radionuclides after the Chernobyl accident in the forestal massif of Boreon

    After the reactor accident at Chernobyl, samples of soil, moss, lichen and fern were collected in the forest around the Vesubie valley in the South East fo France and analyzed by low energy photon and gamma spectrometry. Activity concentrations as high as 42.8, 9.4 and 3.8 kBq.m-2 were measured for 137Cs, 134Cs and 106Ru, respectively, in soil, in October 1988. 12Sb and 110mAg were also detected. The contamination was found to be the most important between 1400 and 1700 m altitude. (author) 9 refs.; 5 figs.; 2 tabs

  14. Silica aerogel Cerenkov detectors for particle identification

    We present light yield measurements of silica aerogel Cerenkov detectors with photomultiplier readout, showing the light yield dependence of pure and wavelength-shifter-doped silica aerogel on block size using both cosmic muons and electrons from a 106Ru source. We present studies of fluorescent fibers and single photon avalanche diodes, including measurements of attenuation lengths and emission spectra of fibers versus wavelength and tests with a single photon avalanche diode. We show results of the response of a single photon avalanche diode to different light sources. Finally, we discuss a new readout scheme using avalanche photodiodes

  15. Monthly progress report

    This monthly report of the SCPRI exposes an interpretation of the principal results concerning the surveillance of radioactivity in the environment: atmospheric dusts (air at ground level, high altitude air), rainwater, surface water, underground water, irrigation water, drinking water, food chain (milk, plants, cattle, fish), sea water around nuclear plant sites and other sites. The activities of various radioisotopes are presented in tables (7Be, 95Zr and 95Nb, 103Ru, 131I, 137Cs, 140Ba and 140La, 90Sr, 106Ru and 104Rh, 226Ra, 54Mn, U and T). A monthly bibliographic selection is also presented

  16. PMT signal increase using a wavelength shifting paint

    Allada, K; Ou, L; Schmookler, B; Shahinyan, A; Wojtsekhowski, B

    2015-01-01

    We report a 1.65 times increase of the PMT signal and a simple procedure of application of a new wavelength shifting (WLS) paint for PMTs with non-UV-transparent windows. Samples of four different WLS paints, made from hydrocarbon polymers and organic fluors, were tested on a 5-inch PMT (ET 9390KB) using Cherenkov radiation produced in fused silica disks by $^{106}$Ru electrons on a `table-top' setup. The best performing paint was employed on two different types of 5-inch PMTs (ET 9390KB and XP4572B), installed in atmospheric pressure CO$_2$ gas Cherenkov detectors, and tested using GeV electrons.

  17. Report on the intercomparison run IAEA-308 radionuclides in seaweed mixture

    The results of an intercomparison exercise on a sample of mixed seaweeds from the Mediterranean Sea, IAEA-308, designed for the determination of artificial and natural radionuclide levels, are reported. The data from 67 laboratories representing 33 countries have been evaluated. The recommended median values, with confidence intervals, for the most frequently measured radionuclides 106Ru, 110mAg, 134Cs, 137Cs, 238Pu, 239+240Pu, 241Am, 40K, 210Pb and 228Th are given. Refs and tabs

  18. Report on the intercomparison run IAEA-307 radionuclides in sea plant

    The results of an intercomparison exercise on a Mediterranean Sea plant sample, coded as IAEA-307, designed for the determination of artificial and natural radionuclide levels, are reported. This sample was collected along the shore from the vicinity of the Principality of Monaco in October 1986. The data from 66 laboratories representing 31 countries have been evaluated. The most frequently measured radionuclides: 106Ru, 110mAg, 134Cs, 137Cs, 238Pu, 239+240Pu, 241Am, 40K and 226Ra. 10 refs, 38 tabs

  19. Review of literature on bioassay methods for estimating radionuclides in urine

    Bioassay methods of certain important radionuclides encountered in the nuclear fuel cycle operations, viz., thorium, uranium, sup(239)Pu, sup(241)Am, sup(90)Sr, sup(99)Tc, sup(106)Ru, sup(137)Cs are reviewed, with special emphasis on urinalysis. Since the preconcentration is an important prerequisite for bioassay, various preconcentration methods are also discussed. Brief account of various instruments both nuclear and analytical used in the bioassay programme is included. The sensitivities of the methods cited in the literature vis-a-vis the derived recording levels indicated in ICRP recommendations are compared. Literature surveyed up to 1990 is tabulated. (author). 96 refs., 1 fig ., 3 tabs

  20. 4. Quarterly progress report, 1978

    This report of the SCPRI exposes an interpretation of the principal results concerning the surveillance of radioactivity in the environment: atmospheric dusts, rainwater, surface water, underground water, irrigation water, drinking water, food chain, sea water around nuclear plant sites and other sites. The activities of various radioisotopes are presented in tables (7Be, 95Zr and 95Nb, 103Ru, 131I, 137Cs, 140Ba and 140La, 90Sr, 106Ru and 106Rh, 226Ra, 54Mn, U and T). A bibliographic selection is also presented

  1. New results from an imaging CCD used as a position sensitive detector at standard TV rate and room temperature

    This paper shows new and improved results, with respect to previous work, regarding the use of an area imaging CCD (Fairchild CCD 222 running at standard TV rate and at 296 K) as X-ray and charged particle detector. A more dedicated video processor is used and as a consequence single pixel signals, revealing X-rays from a 55Fe source and β-rays from a 106Ru source, can be processed, on the basis of the dark average response and of the rms noise of each pixel. Tests are reported concerning the correlation of the signals with the dark current pattern and with the low light level illumination. (orig.)

  2. Solidification and storage of Savannah River Plant radioactive waste

    A conceptual process for solidification of SRP aqueous waste into high-integrity, low-leachable forms was developed. The process separates about 99.9 percent of the biological hazard from approximately 97 percent of the waste. The major biological hazard remaining in the residual salt is 106Ru, which has a 369-day half-life. Sludge and zeolite can be solidified into concrete or glass. Cost-risk analyses are being made to determine which of these forms is preferred for SRP waste. Also, studies on other parts of the conceptual process are in progress. (auth)

  3. 2. Quarterly progress report, 1981

    This report of the SCPRI exposes an interpretation of the principal results concerning the surveillance of radioactivity in the environment: atmospheric dusts, rainwater, surface water, underground water, irrigation water, drinking water, food chain, sea water around nuclear plant sites and other sites. The activities of various radiosotopes are presented in tables (7Be, 95Zr and 95Nb, 103Ru, 131I, 137Cs, 140Ba and 140La, 90Sr, 106Ru and 106Rh, 226Ra, 54Mn, U and T). A bibliographic selection is also presented

  4. 2. Quarterly progress report, 1978

    This report of the SCPRI exposes an interpretation of the principal results concerning the surveillance of radioactivity in the environment: atmospheric dusts, rainwater, surface water, underground water, irrigation water, drinking water, food chain, sea water around nuclear plant sites and other sites. The activities of various radioisotopes are presented in tables (7Be, 95Zr and 95Nb, 103Ru, 131I, 137Cs, 140Ba and 140La, 90Sr, 106Ru and 106Rh, 226Ra, 54Mn, U and T). A bibliographic selection is also presented

  5. 1. Quaterly progress report, 1979

    This report of the SCPRI exposes an interpretation of the principal results concerning the surveillance of radioactivity in the environment: atmospheric dusts, rainwater, surface water, underground water, irrigation water, drinking water, food chain, sea water around nuclear plant sites and other sites. The activities of various radioisotopes are presented in tables (7Be, 95Zr and 95Nb, 103Ru, 131I, 137Cs, 140Ba and 140La, 90Sr, 106Ru and 106Rh, 226Ra, 54Mn, U and T). A bibliographic selection is also presented

  6. 2. Quarterly progress report, 1977

    This report of the SCPRI exposes an interpretation of the principal results concerning the surveillance of radioactivity in the environment: atmospheric dusts, rainwater, surface water, underground water, irrigation water, drinking water, food chain, sea water around nuclear plant sites and other sites. The activities of various radioisotopes are presented in tables (7Be, 95Zr and 95Nb, 103Ru, 131I, 137Cs, 140Ba and 140La, 90Sr, 106Ru and 106Rh, 226Ra, 54Mn, U and T). A bibliographic selection is also presented

  7. Monthly progress report

    This monthly report of the SCPRI exposes an interpretation of the principal results concerning the surveillance of radioactivity in the environment: atmospheric dusts (air at ground level, high altitude air), rainwater, surface water, underground water, irrigation water, drinking water, food chain (milk, plants, cattle, fish), sea water around nuclear plant sites and other sites. The activities of various radioisotopes are presented in tables (7Be, 95Zr and 95Nb, 103Ru, 131I, 137Cs, 140Ba and 140La, 90Sr, 106Ru and 106Rh, 226Ra, 54Mn, U and T). A monthly bibliographic selection is also presented

  8. Hodoscope module with miniature photomultipliers

    The experimental Scintillation Magnetic Spectrometer (SMS) installation, whose main element is an extended hodoscope system, is being built for the accelerator of the High Energy Laboratory of the Joint Institute for Nuclear Research. The authors describe the scintillation hodoscope of the SMS installation and present the applicable amplitude and time characteristics of several types of miniature photomultipliers (FEU-58, FEU-60, FEU-114-1, FEU-147-1, and R-1635 (Hamamatsu, Japan)), which were obtained with a 106Ru radioactive source and standard plastic scintillators of two types, based on oxazoles in polystyrene and in polymethylmethacrylate

  9. Recovery of nitric acid from simulated acidic high level radioactive waste using pore-filled anion exchange membranes

    Acidic waste is generated at different stages of nuclear fuel cycle. The waste contains minor amounts of actinides (241Am, Pu, Np) along with large number of long-lived radionuclides such as 137Cs, 90Sr, 106Ru etc. Before disposal or storage, the overall activity of the waste needs to be reduced. Along with this, the high amount of acid present in the waste needs to be removed. In this study, DD has been used to recover nitric acid from acidic solutions with compositions similar to radioactive waste using pore-filled anion exchange membranes

  10. PMT signal increase using a wavelength shifting paint

    We report a 1.65 times increase of the PMT signal and a simple procedure of application of a new wavelength shifting (WLS) paint for PMTs with non-UV-transparent windows. Samples of four different WLS paints, made from hydrocarbon polymers and organic fluors, were tested on a 5-in. PMT (ET 9390KB) using Cherenkov radiation produced in fused silica disks by 106Ru electrons on a ‘table-top’ setup. The best performing paint was employed on two different types of 5-in. PMTs (ET 9390KB and XP4572B), installed in atmospheric pressure CO2 gas Cherenkov detectors, and tested using GeV electrons

  11. Monthly progress report

    This monthly report of the SCPRI exposes an interpretation of the principal results concerning the surveillance of radioactivity in the environment: atmospheric dusts(air at ground level, high altitude air), rainwater, surface water, underground water, irrigation water, drinking water, food chain (milk, plants, cattle, fish), sea water around nuclear plant sites and other sites. The activities of various radioisotopes are presented in tables (7Be, 95Zr and 95Nb, 103Ru, 131I, 137Cs, 140Ba and 140La, 90Sr, 106Ru and 106Rh, 226Ra, 54Mn, U and T). A monthly bibliographic selection is also presented

  12. Studies on screening of adsorbents for up-take of radioruthenium during vitrification of high-level radioactive waste

    106Ru (T1/2 = 369 days) and 103Ru (T1/2 = 39.3 days) are high specific activity fission products present in different types of nuclear waste generated during the reprocessing of spent nuclear fuel. A major part of it converts into RuO4 vapour during vitrification of high-level waste. Different types of materials like zeolite, perchloric acid treated siliceous brick, stainless steel, polythene, polypropylene, silicone were used as an adsorbent where RuO4 reduced to RuO2 and gets deposited on them which subsequently minimizes the spread of contamination. (author)

  13. Programs and procedures for assessing quality of spectral gamma-ray borehole data for the UGTA

    This report describes the procedures and computer programs used to process spectral gamma-ray borehole logging data in the UGTA (UnderGround Test Area) program at the NTS (Nevada Test Site) to assess data quality. These programs and procedures were used to analyze data from five boreholes in the UGTA program. Development of these computer programs and procedures required considerable effort and the primary purpose of this report is to provide continuity with future activities related to spectral gamma-ray borehole logging in the UGTA program. This is especially important because of the long time interval between cessation of logging in April, 1996 and the next round of activity, which has not yet occurred. This report should also be useful if any quality control issues arise regarding past or forthcoming spectral gamma-ray log analyses. In the characterization work underway at the Nevada Test Site Underground Test Area, the logging contractor, Western Atlas, agreed to identify five artificial nuclides based on their gamma-ray signatures. Those nuclides are 60Co, 106Ru, 125Sb, 134Cs, and 137Cs. In the case of 106Ru, which is not a gamma emitter, any detected gamma rays come from the daughter nuclide 106Rh which has a half-life of 30 s. With such a short half-life, 106Rh can be considered to be in equilibrium with 106Ru under most conditions so the result is the same as if the gamma rays were emitted by the 106Ru. The Western Atlas spectral gamma-ray curve plots from a given borehole present detailed qualitative information on the apparent distribution of natural and artificial nuclides with depth in the borehole. The computer programs and procedures described in this report were used to provide a quality analysis of the contractor's processed data and to work with the contractor to validate and/or refine their existing automatic processing. This was done using a procedure that was developed and tested successfully in earlier work at the NTS; the revised and updated

  14. 3. Quarterly progress report, 1981

    This report of the SCPRI exposes an interpretation of the principal results concerning the surveillance of radioactivity in the environment: atmospheric dusts, rainwater, surface water, underground water, irrigation water, drinking water, food chain, sea water around nuclear plant sites and other sites. The activities of various radioisotopes are presented in tables (7Be, 95Zr and 95Nb, 103Ru, 131I, 137Cs, 140Ba and 140La, 90Sr, 106Ru and 106Rh, 226Ra, 54Mn, U and T). A bibliographic selection is also presented

  15. Study of the radfioisotopic composition of rain in 2.05 1986 in Bucharest-Magurele area

    The paper presents the activities of radionuclides in the rain that fell in Bucharest-Magurele area on May 2nd, 1986. The artificial radionuclides measured were: Sr-89, Sr-90, Ru-103, Ru-106, Sb-125, I-131, (I+Te)-132, Cs-134, Cs-137, (Ba+La)-140, Ce-141, Ce-144, originating in the nuclear accident at Chernobyl. The activities of I-131 and Cs-137 were 28700 Bq/m2 and 3610 Bq/m2 respectively. (authors)

  16. Nuclear Decay Data for the International Reactor Dosimetry Library for Fission and Fusion (IRDFF): Updated Evaluations of the Half-Lives and Gamma Ray Intensities

    Chechev, Valery P.; Kuzmenko, Nikolay K.

    2016-02-01

    Updated evaluations of the half-lives and prominent gamma ray intensities have been presented for 20 radionuclides - dosimetry reaction residuals. The new values of these decay characteristics recommended for the IRDFF library were obtained using the approaches and methodology adopted by the working group of the Decay Data Evaluation Project (DDEP) cooperation. The experimental data published up to 2014 were taken into account in updated evaluations. The list of radionuclides includes 3H, 18F, 22Na, 24Na, 46Sc, 51Cr, 54Mn, 59Fe, 57Co, 60Co, 57Ni, 64Cu, 88Y, 132Te, 131I, 140Ba, 140La, 141Ce, 182Ta, 198Au.

  17. Deposition and retention of radioactive aerosols on desert vegetation

    Deposition velocities and retention times were obtained for submicron aerosols of 134Cs and 141Ce on a shrub species (Artemisia tridentata) and a grass (Elymus elimoides) in a natural desert environment. Submicron aerosols of these two nuclides were artificially generated and released over a sagebrush community in southeast Idaho during each of three seasons: spring, summer and winter, to determine the effects of weathering and plant development on aerosol deposition and retention. Information on friction velocities, roughness lengths, and particle size was also obtained

  18. Reconstruction of dose on the basis of forest litter activity measurements (case studies)

    In a large scale investigation of Polish forest litter contamination performed in recent years we observed the variety of Chernobyl fallout in Poland. Besides large differences in the radiocaesium contamination levels, we found a non-uniform isotopic composition of the fallout; in the north-eastern part of the country we found enhanced (relative to caesium) amounts of non-volatile radioisotopes. We were still able to detect 144Ce, 154Eu and 155Eu as well as plutonium isotopes of Chernobyl origin. 7 refs

  19. Radionuclide volatilization during plasmachemical reprocessing of radioactive wastes

    Volatilization of 137Cs, 60Co, 90Sr, 144Ce and α-active radionuclides under high temperature utilization of solid and liquid low- and intermediate level radioactive wastes is studied. Low temperature plasma of arc plasmatroned was used as a heat carrier in the laboratory conditions and on experimental installation with shaft furnace and direct flow plasma-chemical reactor. The lowest radionuclides lost (1-2%) was observed from the shaft furnace due to the presence of radionuclides sorbiting layer of wastes

  20. The dispersion of pollutants in the Romanian rivers Olt, Somes and Danube

    The paper describes the results obtained in three tracer experiments carried out into the Romanian rivers Olt and Somes as well as into the Romanian part of the Danube by using the radioactive tracer 82Br. The possibility of a radioactive discharge to occur from the Cernavoda Nuclear Power Plant bring to focus also knowing of the distribution of fission products between water and solid suspended material. Consequently there were also studied and presented the distribution coefficients of the radionuclides 131I, 99Mo, 144Ce, 137Cs, and 95Zr for clay, loess and the particular alluvium collected from the Danube bed. (author)

  1. Life-span health effects of relatively soluble forms of internally deposited beta-emitting radionuclides

    As part of a large research effort to study the lifetime health risks of inhaled radionuclides, Beagle dogs inhaled 90SrCl2 or 144CeCl3 or were injected intravenously with 137CsCl. Because these three compounds were soluble in body fluids, the resulting widely differing patterns of radionuclide distribution and dose reflected tissue affinities of the elements involved. Long-term health effects, predominantly cancers, were seen in the organs receiving the highest doses. Investigations are continuing on the extent to which other less irradiated organs may have also been affected

  2. Appendix to Health and Safety Laboratory environmental quarterly report. [Fallout radionuclides deposited and in surface air at various world sites; /sup 137/Cs and /sup 90/Sr in milk and drinking water in New York City; and stable Pb in surface air

    Hardy, E.P. Jr.

    1977-07-01

    Tabulated data are presented on the deposition of fallout /sup 89/Sr and /sup 90/Sr at various world land sites through 1976; the ..gamma.. spectra and content of /sup 7/Be, /sup 95/Zr, /sup 137/Cs, /sup 144/Ce, /sup 90/Sr, /sup 210/Pb, /sup 238/Pu, /sup 239/Pu, and stable Pb in samples of surface air collected during 1966 at various world sites; and the content of fallout /sup 137/Cs and /sup 90/Sr in samples of drinking water and milk collected in New York City through 1976. (CH)

  3. Chelating agents in pharmacology, toxicology and therapeutics

    The proceedings contain 71 abstracts of papers. Fourteen abstracts were inputted in INIS. The topics covered include: the effects of chelating agents on the retention of 63Ni, 109Cd, 203Hg, 144Ce, 95Nb and the excretion of 210Po, 63Ni, 48V, 239Pu, 241Am, 54Mn; the applications of tracer techniques for studies of the efficacy of chelation therapy in patients with heart and brain disorders; and the treatment of metal poisoning with chelating agents. (J.P.)

  4. Migration studies of radionuclides at the WIPP site

    A study was made of the effects on radionuclide migration from the solid TRU waste of inorganic and organic ligands in brine media. Typical organic waste meterials were exposed to synthetic brine at 700 for up to 1 year. Pure brine and brine/organic waste extracts were used to determine actinide and lathanide (153Gd, 144Ce, 152Eu, 243Am) distribution coefficients K/sub d/ between geological media and the brine. Results show that brine containing extract from plywood, etc. reduces considerably the K/sub d/

  5. Distribution of radionuclides among green alga, marine sediments and sea water

    Distributions of radionuclides among green alga (Ulva pertusa), marine sediment and sea water were examined in laboratory experiments with radioisotope tracers to look into the behavior of the radionuclides released into the coastal sea. Marine sands from the five different seashores along the coast of Japan were used. Distributions of 60Co, 95Zr-95Nb and 106Ru-106Rh in these sands were by far the highest of the three components (marine sand, sea water and marine alga). The distributions of the three radionuclides had not so large fluctuations among the five marine sands and were considered to be rather constant. The total amount found in marine sand and green alga was about 90% for the three radionuclides but about 20% for 137Cs on the average in two weeks after the start of the experiments. The activity ratio of marine sediment (radioactivity in 1 g of sediment/radioactivity in 1 ml of sea water) was 4000 for 60co, 30 for 137Cs, 1800 for 95Zr-95Nb and 900 for 106Ru-106Rh. (auth.)

  6. The impact of Chernobyl fallout on Mytilus sp. collected from the French coast

    The spatial distributions of 103Ru, 106Ru, 110mAg, 134Cs and 13/Cs levels in Mytilus sp. samples gathered from the entire French coast subsequent to the explosion of unit 4 at the Soviet nuclear power plant in Chernobyl are largely in line with those based on aerosol and terrestrial measurements. Thus measurements of this bio-indicator found Channel levels to be lower by a factor of 10 than those observed on the eastern section of the Mediterranean coasts. Areas subject to chronic low-level industrial radioactive discharges, such as the Cotentin shoreline and the Rhone estuary, display a slight increase of 106Ru and 137Cs radioactivity levels. In contrast, contamination is especially clear-cut in areas initially free from radionuclides (i.e. surrounding Nice) where biological removal with time has been characterized and modelized, for both ruthenium isotopic forms, and covering 10 and 94 day biological periods. These data, when compared with those found in the literature, indicate that the memorizing time in the event of an accidental release of ruthenium is shorter than for chronic releases. An assessment of public health implications following the ingestion of mussels labelled solely by Chernobyl fallout is of the same order of magnitude as that of mussels gathered in an area exposed to Rhone industry, i.e. 10-5 of the annual dose limit to the whole body for the public at large

  7. Separation of 90Sr from PUREX HLLW using N,N,N',N'-tetra (2-ethylhexyl)diglycolamide

    This paper describes the separation of 90Sr from PUREX-HLLW employing separation techniques viz. solvent extraction and precipitation. In the first step, PUREX-HLLW was subjected to solvent extraction using TBP (30% in n-dodecane) to remove residual uranium and plutonium. In the subsequent step the raffinate was treated with N,N,N',N'-tetra (2-ethylhexyl) diglycolamide (TEHDGA, 0.20M in 30% isodecyl alcohol and n-dodecane) for the bulk separation of trivalent actinides and lanthanides. The raffinate from this step containing major activity of 90Sr and other fission products such as 137Cs and 106Ru etc. forms ideal feed for 90Sr recovery. Strontium from this non alpha bearing HLLW was extracted using 0.30M TEHDGA in 5% isodecyl alcohol and n-dodecane and stripped with 0.01M HNO3. Recovery of 90Sr was found to be quantitative which was further purified from trace impurities such as 106Ru etc. and concentrated using radiochemical precipitation technique employing Fe scavenging as hydroxide followed by carbonate precipitation after adding natural Fe and Sr as carriers

  8. Screening of silver nanoparticles containing carbonized yeast cells for adsorption of few long-lived active radionuclides

    The present study involves the screening of silver nanoparticles containing carbonized yeast cells isolated from coconut cell sap for efficient adsorption of few long lived radionuclides like 137Cs55, 60Co27, 106Ru44, 239Pu94 and 241Am95. Yeast cells containing silver nanoparticles produced through biological reduction were subjected to carbonization (400 deg C for 1 h) at atmospheric conditions and their properties were analyzed using fourier transform infra-red spectroscopy, X-ray diffraction, scanning electron microscope attached with energy dispersive spectroscopy and transmission electron microscope. The average size of the silver nanoparticles present on the surface of the carbonized silver containing yeast cells (CSY) was 19 ± 9 nm. The carbonized control yeast cells without silver exposure (CCY) did not contain any particles on its surface. The efficiency of CSY and CCY towards the radionuclide adsorption was studied in batch mode at fixed contact time, concentration, and at its native pH. CSY was efficient in removal of 239Pu94 (76.75%) and 106Ru44 (54.73%) whereas CCY showed efficient removal only for 241Am95 (62.89%). Both the adsorbents did not show any retention with respect to 60Co27 and 137Cs55. Based on the experimental data, decontamination factor and distribution coefficient (Kd) were calculated and, from the values, it was observed that these adsorbents have greater potential to adsorb radionuclides. (author)

  9. Monte Carlo-based Bragg-Gray tissue-to-air mass-collision-stopping power ratios for ISO beta sources

    Quantity of interest in external beta radiation protection is the absorbed dose rate to tissue at a depth of 7 mg/cm2 Dt (7 mg/cm2) in a 4-element ICRU (International Commission for Radiation Units and Measurements) unit density tissue phantom. ISO (International Organization for Standardization) 6980-2 provides guidelines to establish this quantity for beta emitters using an extrapolation chamber as a primary standard. ISO 6980-1 proposes two series of beta reference radiation fields, namely, series 1 and series 2. Series 1 covers 90Sr/90Y, 85Kr, 204Tl and 147Pm sources used with beam flattening filter and Series 2 covers 14C and 106Ru/106Rh sources used with beam flattening filter. Dt (7 mg/cm2) is realized based on measured current and set of corrections including Bragg-Gray tissue-to-air mass-stopping power ratio, (S/ρ)t,a. ISO provides (S/ρ)t,a values which are based on approximate methods. The present study is aimed at calculating (S/ρ)t,a for 90Sr/90Y, 85Kr, 106Ru/106Rh and 147Pm sources using the Monte Carlo (MC) methods and compare the same against the ISO values. By definition, (S/ρ)t,a should be independent of cavity length of the chamber which was verified in the work

  10. Monte Carlo-based Spencer-Attix and Bragg-Gray tissue-to-air stopping power ratios for ISO beta sources

    Spencer-Attix (SA) and Bragg-Gray (BG) mass-collision-stopping-power ratios of tissue-to-air are calculated using a modified version of EGSnrc-based SPRRZnrc user-code for the International Organization for Standardization (ISO) beta sources such as 147Pm, 85Kr, 90Sr/90Y and 106Ru/106Rh. The ratios are calculated at 5 and 70 μm depths along the central axis of the unit density ICRU-4-element tissue phantom as a function of air-cavity lengths of the extrapolation chamber l = 0.025-0.25 cm. The study shows that the BG values are independent of l and agree well with the ISO-reported values for the above sources. The overall variation in the SA values is ∼0.3 % for all the investigated sources, when l is varied from 0.025 to 0.25 cm. As energy of the beta increases the SA stopping-power ratio for a given cavity length decreases. For example, SA values of 147Pm are higher by ∼2 % when compared with the corresponding values of 106Ru/106Rh source. SA stopping-power ratios are higher than the BG stopping-power ratios and the degree of variation depends on type of source and the value of l. For example, the difference is up to 0.7 % at l = 0.025 cm for the 90Sr/90Y source. (authors)