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Abstract  

The radioactivity induced in rock slices during fission track analysis for uranium can usefully be employed in instrumental neutron activation analysis for determination of major and trace element distributions in the sample using a collimated gamma spectrometer. A description is given of the application of particle track techniques in conjunction with activation analysis to a geochemical study of element migration in a sample of mineralized granite from Nigeria. The study indicates that U is enriched during the earlier period of rock-fluid interaction (microclinization) and that Th is enriched during greisenization.

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Abstract  

The concentrations of Th in samples of crystalline rock from three drillcore sections were analysed independently by instrumental neutron activation analysis and by chemical separation and alpha spectroscopy. The two methods show good general agreement over an approximate concentration range of 1 to 100 ppm Th. Variations in results between the two methods are not of a systematic nature and probably arise from sample heterogeneity. The results confirm the reliability of both methods and provide a useful comparison of the standards and reference materials used. The study indicates that, in cases where Th isotopic information is not required, the simpler and more rapid neutron activation analysis provides a satisfactory method.

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Abstract  

Scintillation cocktail components were studied with regard to their impact on pulse decay discimination (PDD) and hence the separation of alpha from beta activity, using a Packard 2250 CA /. Di-isopropyl naphthalene (DIN) was found to be the most suitable solvent, both from safety considerations and also the fact that it acts in a very similar manner to naphthalene in stretching the pulses produced at the photomultiplier tube anode and hence enhancing the separation. Increasing the surfactant concentration and the use of dimethylanthracene (DMA) as secondary fluor degraded the cocktail's performance. PMT anode pulse shapes were found to be a useful indicator of PDD efficiency but could not give a quantitative guide.

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Abstract  

Multi-radionuclide analyses of coastal marine sediments and seawater can be of considerable value in defining rates and mechanisms of nearshore processes. A preliminary study of134Cs,137Cs,210Pb,226Ra and228Ra in the Clyde Sea Area has been performed. A summary of the marine geochemistries of these species and a detailed account of methods involved in their routine analysis are described.

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Journal of Thermal Analysis and Calorimetry
Authors:
R. Mackenzie
,
C. Keattch
,
D. Dollimore
,
J. Forrester
,
A. Hodgson
, and
J. Redfern
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Abstract  

Results are repoerted for238U,234U,232Th, and230Th determinations in 19 rock samples from a uranium mine, performed independently, byb three different laboratories. Uranium and thorium isotopoic activities were determkined by alpha spectrometry, after different pre-concentration and counting sample preparation techniques., Additionally, total concentrations of uranium were determined by fluorimetry and gamma spectreometry. the folloing conclusions could be drawn from this intercomparison test: (1) The results for238U specific activity agreed with the amjority of results within 10%. Lincar correlation coefficients between the three data sets were 0.999. However, for a few samples of much higher uranium concentrations, large deviations were observed, indicating problems of, sample heterogencity. (2) For the234U/238U activity ratio data, a still closer agreement was obtained (5%), as computation of the activity ratios did not, require information on the yield of the used tracer spike (232U). (3) The results for232Th specific activities and230Th/234U activity ratios showed larger deviastions between the three laboratories (typically up to 15%, in some cases still ore). Different Th-isotopes (228Th,234Th and229Th) have been used as yield tracers. The data indicates, however, that the observed deviations are not simply a consequence of a systematic difference in the calibration of the different spikes, but, probably cased by other errors such as incomplete sample dissolution, sample heterogencity, tec. The limitations of alpha spectrometry will be discussed and an application of the developed methods shown.

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Journal of Radioanalytical and Nuclear Chemistry
Authors:
G. Cook
,
E. Scott
,
A. MacKenzie
,
F. Naysmith
,
K. Isogai
,
P. Kershaw
,
R. Anderson
, and
P. Naysmith

Abstract  

Prior to 1984, the reported marine 14C discharges from Sellafield were estimates: 0.2 TBq per annum from 1952 to 1969 and 1 TBq per annum until 1984 when measurements commenced. The relationship between the net excess 14C activity in annually collected Nori (Porphyra umbilicalis) seaweed samples and the annual discharges (estimated and measured) implies that the discharges were not as constant as the estimates. Based on the relationship between post-1984 measured discharges and the excess 14C in the seaweed, two simple empirical models were used to re-calculate the discharges between 1967 and 1984. Gamma-spectrometry measurements on the seaweed also indicate that Porphyra is a sensitive indicator of changes in discharge of other radionuclides, brought about by the introduction of new waste clean-up technologies within Sellafield.

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