TY - BOOK
T1 - Geochemistry of natural radionuclides in uranium-enriched river catchments
AU - Siddeeg, Saif Eldin Mohammed Babiker
PY - 2013
Y1 - 2013
N2 - Radionuclides from natural U-series in sediments from two river catchments in the UK have been studied. The aim was to gain insight into the behaviour of 238U, 234U, 230Th and 226Ra in real natural systems enriched in uranium. A radiochemical method for radium separation followed by alpha spectrometric measurement has been developed. The method allowed use of 225Ra, in equilibrium with the parent 229Th, as a yield determinant, and has been applied in 226Ra concentrations measurements in the selected areas of study.U-series progeny, 238U, 234U, 230Th and 226Ra, in totally dissolved sediments from the valley of the River Noe and the fraction leached by aqua regia, have been measured. Total sediment contents ranged from 9 ± 2 to 184 ± 8 Bq.kg-1 for uranium, 9 ± 3 to 200 ± 13 Bq.kg-1 for thorium and 18 ± 1 to 179 ± 8 Bq.kg-1 for radium. The activity concentrations in the leached fractions, compared with the total, were 46% for uranium, 54% for thorium and 56% for radium, on average. The radionuclides showed extensive disequilibrium and this suggested a complex leaching/accumulation of uranium as well as an impact of organic matter and secondary minerals.Uranium and radium have been geochemically characterised in sediments from near the South Terras abandoned uranium mine, Cornwall. Background activity concentration levels of uranium in sediments ranged from 13 ± 3 to 290 ± 14 Bq.kg-1, with radium from 42 ± 4 to 424 ± 23 Bq.kg-1. Elevated concentrations of uranium and radium were measured in two samples, S3 with 1820 ± 36 Bq.kg-1 for uranium and 940 ± 53 Bq.kg-1 for radium; and S7 with 4350 ± 53 Bq.kg-1 for uranium and 1765 ± 48 Bq.kg-1 for radium. Sequential chemical extraction for the two samples revealed that both uranium and radium were associated with organic and carbonate fractions, with 25 % of the uranium in the resistant phase of S7. 234U/238U activity ratios of the sequential extraction fractions showed different trends in the sediments, and this was linked to the impact of organic matter and/or exchange between water and sediment. Uranium-bearing minerals in association with potassium, calcium, iron, manganese and arsenic have been identified in these sediments.
AB - Radionuclides from natural U-series in sediments from two river catchments in the UK have been studied. The aim was to gain insight into the behaviour of 238U, 234U, 230Th and 226Ra in real natural systems enriched in uranium. A radiochemical method for radium separation followed by alpha spectrometric measurement has been developed. The method allowed use of 225Ra, in equilibrium with the parent 229Th, as a yield determinant, and has been applied in 226Ra concentrations measurements in the selected areas of study.U-series progeny, 238U, 234U, 230Th and 226Ra, in totally dissolved sediments from the valley of the River Noe and the fraction leached by aqua regia, have been measured. Total sediment contents ranged from 9 ± 2 to 184 ± 8 Bq.kg-1 for uranium, 9 ± 3 to 200 ± 13 Bq.kg-1 for thorium and 18 ± 1 to 179 ± 8 Bq.kg-1 for radium. The activity concentrations in the leached fractions, compared with the total, were 46% for uranium, 54% for thorium and 56% for radium, on average. The radionuclides showed extensive disequilibrium and this suggested a complex leaching/accumulation of uranium as well as an impact of organic matter and secondary minerals.Uranium and radium have been geochemically characterised in sediments from near the South Terras abandoned uranium mine, Cornwall. Background activity concentration levels of uranium in sediments ranged from 13 ± 3 to 290 ± 14 Bq.kg-1, with radium from 42 ± 4 to 424 ± 23 Bq.kg-1. Elevated concentrations of uranium and radium were measured in two samples, S3 with 1820 ± 36 Bq.kg-1 for uranium and 940 ± 53 Bq.kg-1 for radium; and S7 with 4350 ± 53 Bq.kg-1 for uranium and 1765 ± 48 Bq.kg-1 for radium. Sequential chemical extraction for the two samples revealed that both uranium and radium were associated with organic and carbonate fractions, with 25 % of the uranium in the resistant phase of S7. 234U/238U activity ratios of the sequential extraction fractions showed different trends in the sediments, and this was linked to the impact of organic matter and/or exchange between water and sediment. Uranium-bearing minerals in association with potassium, calcium, iron, manganese and arsenic have been identified in these sediments.
M3 - Doctoral Thesis
PB - University of Manchester, Faculty of Engineering and Physical Science
ER -