Search Results

You are looking at 1 - 2 of 2 items for

  • Author or Editor: A. Flowers x
  • Refine by Access: All Content x
Clear All Modify Search


This paper describes our development of an accurate determination of uranium by alpha spectrometry using various kinds of sample digestion methods. The sample preparation techniques employed an acid digestion with HNO3, and microwave oven digestion either by HNO3 or by combination of HNO3 and HF. The samples were obtained from surface and in depth(40 cm) soils from residential area. An extraction chromatography column has been used to separate the uranium from interference matrix and elements. Results show that the microwave method significantly speeds up the analysis time, reduces the volume of acids used and eliminates a large fraction of acid vapour emission. Compared with the uranium recoveries it was shown that microwave HNO3+HF achieved greater recovery (83%) than microwave HNO3 (78%), while less obtained by HNO3 digestion using hot plate (75%). Various kind of digestion methods have been applied (24 times) for two kind of soil sample. The reproducibility was acceptable and the average precision (coefficient of variation) was between 4 to 5. No significant differences between the precision of the methods have been observed. Acid volume required for the microwave procedures are a fraction of 5 times lower and the analysis time 6 times lower than traditional digestion by hot plate technique.

Restricted access


A simple method was used to design and set up an electrodeposition device for the alpha-emitting nuclides. The designed electroplating facility is leak proof and simple in operation and dismantled. The effect of current, pH of electrolyte, and the plating time on the electrodeposition efficiency have been investigated in a sodium bisulphate, sulphuric acid electrolyte in order to determine the optimum conditions. It was shown that a current of 900-1000 mA, plating time of 80-90 minutes and pH range of 2-2.3 are the best conditions for deposition of nano-scale uranium and plutonium. In these circumstances, it was possible to deposit 0.004 ng . g-1 Pu and 60 ng . g-1 U in an electroplating planchette. The device and modified procedures were successfully applied for soil samples. Prior to electrodeposition of the elements, a column extraction chromatography has been used to separate the Pu and U and eliminate most matrix and interferences in environmental samples.

Restricted access