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AbstractAbstract
[en] A simple method is described for the isolation and determination of plutonium isotopes in sediments. The method involves leaching of sample with nitric acid and subsequent separation of plutonium on an anion-exchange column. Major matrix elements and several potential radiochemical interferences are removed during 8M HNO3 sample loading on the column. Thorium is removed by thorough washing with 10M HCl. Plutonium(IV) is eluted with 4M HCl. Source for alpha-particle spectrometry is prepared by LaF3 coprecipitation technique at which stage a complete separation from uranium(VI) is also achieved. The entire analytical procedure is completed in about two days. (author)
Primary Subject
Source
20 refs.
Record Type
Journal Article
Journal
Journal of Radioanalytical and Nuclear Chemistry; ISSN 0236-5731; ; CODEN JRNCD; v. 102(1); p. 187-193
Country of publication
ACTINIDE NUCLEI, ACTINIDES, ALPHA DECAY RADIOISOTOPES, CHROMATOGRAPHY, ELEMENTS, EVEN-EVEN NUCLEI, EVEN-ODD NUCLEI, FLUORIDES, FLUORINE COMPOUNDS, HALIDES, HALOGEN COMPOUNDS, HEAVY NUCLEI, ISOTOPES, LANTHANUM COMPOUNDS, METALS, NUCLEI, PLUTONIUM ISOTOPES, PRECIPITATION, RADIOISOTOPES, RARE EARTH COMPOUNDS, SEPARATION PROCESSES, SPECTROSCOPY, TRANSURANIUM ELEMENTS, YEARS LIVING RADIOISOTOPES
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AbstractAbstract
[en] A method is described for the non-destructive determination of 210Pb and 226Ra in sediments. The procedure is based on the direct counting of the 46.5 keV γ-ray of 210Pb and the 351.9 keV γ-emission of 214Pb. The self-absorption of the 46.5 keV γ-ray is corrected using a technique involving direct gamma transmission measurements on sample and efficiency calibration standard. Several reference materials when assayed by the described method yielded results in general agreement with the certified values. The application of the method is illustrated through the analysis of the excess 210Pb profile of a Lake Ontario sediment core. (author) 29 refs.; 3 figs.; 3 tabs
Primary Subject
Record Type
Journal Article
Literature Type
Numerical Data
Journal
Journal of Radioanalytical and Nuclear Chemistry; ISSN 0236-5731; ; CODEN JRNCD; v. 116(1); p. 169-182
Country of publication
ALPHA DECAY RADIOISOTOPES, BETA DECAY RADIOISOTOPES, BETA-MINUS DECAY RADIOISOTOPES, CARBON 14 DECAY RADIOISOTOPES, CHEMICAL ANALYSIS, DATA, DETECTION, DIMENSIONS, DISTRIBUTION, EVEN-EVEN NUCLEI, GREAT LAKES, HEAVY ION DECAY RADIOISOTOPES, HEAVY NUCLEI, INFORMATION, ISOTOPES, LAKES, LEAD ISOTOPES, MINUTES LIVING RADIOISOTOPES, NUCLEI, NUMERICAL DATA, QUANTITATIVE CHEMICAL ANALYSIS, RADIATION DETECTION, RADIOISOTOPES, RADIUM ISOTOPES, SPECTRA, SURFACE WATERS, YEARS LIVING RADIOISOTOPES
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AbstractAbstract
[en] The levels of Chernobyl-derived radionuclides were measured in several rain, snow and water filtration plant floc samples collected from various locations in Canada. The data indicate that the Chernobyl release had negligible effect on the radiological quality of Lake Ontario waters. The detection of some activation products in pre-Chernobyl samples, presumably arising from the accidental release of radioactivity during weapon testing at the Nevada site, is also reported. Some data from the ongoing measurements on rain samples are presented to discuss the possible use of Chernobyl radionuclides for delineating tropospheric transport processes. Fractionation factors for the major radionuclides are also reported. (Auth.)
Primary Subject
Secondary Subject
Source
20 refs.; 5 figs.; 5 tabs.
Record Type
Journal Article
Journal
Country of publication
ACCIDENTS, ATMOSPHERIC PRECIPITATIONS, DEVELOPED COUNTRIES, ENRICHED URANIUM REACTORS, ENVIRONMENTAL TRANSPORT, GRAPHITE MODERATED REACTORS, GREAT LAKES, HYDROGEN COMPOUNDS, LAKES, LWGR TYPE REACTORS, MASS TRANSFER, NORTH AMERICA, OXYGEN COMPOUNDS, POLAR SOLVENTS, POWER REACTORS, REACTORS, SOLVENTS, SURFACE WATERS, THERMAL REACTORS, WATER, WATER COOLED REACTORS
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AbstractAbstract
[en] The chemistry of uranium and its eight associated daughters were considered in Lake Ontario water along with that of selected transuranic elements. These transuranics arise mainly from fallout, and to a lesser extent from nuclear fuel reprocessing. Most exist as free ions or oxides of various kinds, uranium probably exists as a strong uranyl carbonate complex. (author)
Primary Subject
Source
20 refs.; 2 figs.; 2 tables.
Record Type
Journal Article
Journal
Journal of Radioanalytical and Nuclear Chemistry; ISSN 0236-5731; ; CODEN JRNCD; v. 106(6); p. 333-343
Country of publication
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Baweja, A.S.; Joshi, S.R.; Demayo, A.
Department of the Environment, Ottawa, ON (Canada). Inland Waters Branch1987
Department of the Environment, Ottawa, ON (Canada). Inland Waters Branch1987
AbstractAbstract
[en] Water samples were analyzed for total U, Ra-226, Cs-137, Sb-125 and tritium. Levels are generally low, and no time trends were discernible during the monitoring period. Temporal variations among the quarterly analyses are mostly insignificant. Except for total U at certain locations, all other radionuclide levels were much below the 'target concentration' guidelines for Canadian drinking water. The main contribution to the radiological dose commitment was from total U and Ra-226. Contributions from individual radionuclides to cumulative dose were in the order: total U > Ra-226 > tritium > Cs-137 > Sb-125. The limited sediment data suggest that the nuclear facilities along the Ottawa River have increased the levels of Cs-137 and Co-60 but have not affected those of Pb-210 and Ra-226. Total U and Ra-226 activities data suggest disequilibrium; the levels of total U in water were much higher than those of Ra-226. Concentrations of the two radionuclides, however, were positively correlated for most surface waters
Primary Subject
Source
1987; 25 p
Record Type
Report
Report Number
Country of publication
ACTINIDES, ANTIMONY ISOTOPES, BETA DECAY RADIOISOTOPES, BETA-MINUS DECAY RADIOISOTOPES, CESIUM ISOTOPES, DEVELOPED COUNTRIES, ELEMENTS, EVEN-EVEN NUCLEI, HEAVY NUCLEI, HYDROGEN ISOTOPES, INTERMEDIATE MASS NUCLEI, ISOTOPES, LIGHT NUCLEI, MASS TRANSFER, METALS, MINUTES LIVING RADIOISOTOPES, MONITORING, NORTH AMERICA, NUCLEI, ODD-EVEN NUCLEI, RADIOISOTOPES, RADON ISOTOPES, YEARS LIVING RADIOISOTOPES
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AbstractAbstract
[en] A method is described for the determination of 228Th, 230Th, and 232Th in sediments. The analytical protocol employs direct determination of 228Th by high-resolution γ-ray spectrometry. Isotopic ratios are determined by α-particle spectrometric assay of the thorium fraction purified by a simple anion-exchange technique. Three sediment and soil reference materials when analyzed by the described method gave results in general agreement with the certified values. 21 references, 3 figures, 1 table
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Secondary Subject
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Journal Article
Literature Type
Numerical Data
Journal
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AbstractAbstract
[en] Environmental radioactivity is explained for the Canadian non-specialist under the following headings: sources of radiation and their relative significance, disposal of radioactive wastes, environmental distribution, biogeochemical cycling of radionuclides, environmental radionuclides as tracers, radiation and ecosystem health, radiation and human health. The authors conclude that although radiation performs many useful tasks, and remains an integral part of our lives, yet nevertheless some anxiety will remain
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Secondary Subject
Record Type
Journal Article
Journal
Country of publication
ACTINIDE NUCLEI, ALPHA DECAY RADIOISOTOPES, BETA DECAY RADIOISOTOPES, BETA-MINUS DECAY RADIOISOTOPES, BETA-PLUS DECAY RADIOISOTOPES, CARBON 14 DECAY RADIOISOTOPES, CESIUM ISOTOPES, DEVELOPED COUNTRIES, ELECTRON CAPTURE RADIOISOTOPES, ENVIRONMENTAL TRANSPORT, EVEN-EVEN NUCLEI, HEAVY ION DECAY RADIOISOTOPES, HEAVY NUCLEI, INTERMEDIATE MASS NUCLEI, ISOMERIC TRANSITION ISOTOPES, ISOTOPE APPLICATIONS, ISOTOPES, LAKES, LIGHT NUCLEI, MASS TRANSFER, MATERIALS, NORTH AMERICA, NUCLEI, ODD-EVEN NUCLEI, ODD-ODD NUCLEI, POTASSIUM ISOTOPES, RADIOACTIVE MATERIALS, RADIOACTIVE WASTES, RADIOISOTOPES, RADIUM ISOTOPES, STRONTIUM ISOTOPES, SURFACE WATERS, THORIUM ISOTOPES, URANIUM ISOTOPES, WASTES, YEARS LIVING RADIOISOTOPES
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AbstractAbstract
[en] Airborne radioactive materials readily contaminate plant surfaces and thus are incorporated into the food chains. Most of the nuclear fission products and naturally occurring radionuclides in the air are carried on solid particles ranging in size from a few submicrons to several millimetres in diameter. Of many available mechanisms, rainfall plays a dominant role in the deposition and removal of radioactive particles from plants. Mechanisms for the deposition of submicron particles, which carry significant amounts of radioactivity, are still not very well understood. Available information on the physicochemical aspects of the retention of radionuclides by plants is inadequate in explaining radionuclide uptake and desorbability. Much of the work reported so far has been carried out on selected fission products only. There is a dearth of data pertaining to naturally occurring radionuclides, especially 222Rn and its daughters, significant amounts of which are released to the environment during uranium mining and milling operations. Radiation damage in plants is difficult to detect except at levels of contamination thousands of times higher than those attained in most real life situations. Existing reports give conflicting accounts of the damage induced by low-level radiation in plants. The literature data discussed in this review are presented as basic information needed for the conduct and interpretation of useful research. (orig.)
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Record Type
Journal Article
Journal
Science of the Total Environment; ISSN 0048-9697; ; v. 24(2); p. 101-198
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Joshi, S.R.
Environmental impact of coal utilization (from raw material to waste resources): Proceedings1991
Environmental impact of coal utilization (from raw material to waste resources): Proceedings1991
AbstractAbstract
[en] The coal available in India for use in coal-burning thermal power plants is of a very inferior quality. It has a low calorific value and a high ash content (40 to 50%). Consequently Indian thermal power plants produce large quantities of fly ash which is disposed as waste. The thermal power plants of the Maharashtra State Electricity Board (MSEB) dispose fly ash by wet disposal method. This method requires large areas of land which are lost to agriculture or forestation. Construction of earthen bunds to make disposal areas requires clay soil which is generally top fertile soil. This also affects agriculture adversely. Moreover the effluent water from ash disposal areas is found to be polluted with suspended solids beyond acceptable limits. MSEB is trying to minimise these adverse environmental impacts by: (1)using fly ash as hearting material to construct bunds, (2) raising tree plantations on ash-filled areas, (3) using effluent water to irrigate forestry or tree plantations, (4) recirculation of ash water, and (5) establishing coal washeries at the site of collieries. This last measure will reduce consumption of fuel required for coal transport and also reduce transportation cost. (M.G.B.). 5 refs
Primary Subject
Source
Sahu, K.C. (ed.) (Indian Inst. of Science, Bangalore (India). Dept. of Civil and Hydraulic Engineering); 301 p; Oct 1991; p. 207-211; Indian Institute of Technology; Bombay (India); International conference on environmental impact of coal utilization; Bombay (India); 14-15 Jan 1991
Record Type
Book
Literature Type
Conference
Country of publication
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Related RecordRelated Record
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AbstractAbstract
[en] Four possible sources of analytical error in the measurement of unsupported 210Pb and/or nuclear fallout radionuclide (such as 137Cs) profiles in sediment core are (1) Freezing the entire sediment core prior to precise sectioning; (2) Sectioning the sediment core at room temperature or lower; (3) Determining 210Pb via its 5.01-day half-life beta emitting daughter 210Bi; (4) Determining 210Pb via the 138-day alpha-emitting granddaughter 210Pb. Simple procedural modifications can substantially improve the quality of analytical data that are subsequently used to develop intricate mathematical models to aid the interpretation of observed radionuclide profiles. These modifications include (1) Always store subsamples for sufficiently long periods of time to ensure equilibrium between 210Po and unsupported 210Pb; (2) Always use 208Po as yield monitor and assay autoplated sources on an alpha-particle counter since the alpha particle energies of 208Po and 210Po are separable only on a spectrometer using a detector; (3) Never use any glassware for radiochemical work involved polonium since several polonium compounds are known to absorb onto glass surfaces. Quartz is perhaps the best choice though Teflon or similar materials are also suitable for most situations. Avoid heating above 120 C during HCl leaching and above 90 C during plating since PoCl4 is highly volatile
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Record Type
Journal Article
Journal
Country of publication
AGE ESTIMATION, ALPHA DECAY RADIOISOTOPES, BETA DECAY RADIOISOTOPES, BETA-MINUS DECAY RADIOISOTOPES, BISMUTH ISOTOPES, CESIUM ISOTOPES, DAYS LIVING RADIOISOTOPES, ECOLOGICAL CONCENTRATION, ELECTRON CAPTURE RADIOISOTOPES, EVEN-EVEN NUCLEI, HEAVY NUCLEI, INTERMEDIATE MASS NUCLEI, ISOMERIC TRANSITION ISOTOPES, ISOTOPES, LEAD ISOTOPES, MEASURING INSTRUMENTS, MONITORING, NUCLEI, ODD-EVEN NUCLEI, ODD-ODD NUCLEI, POLONIUM ISOTOPES, RADIOISOTOPES, YEARS LIVING RADIOISOTOPES
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