Результаты исследований: Научные публикации в периодических изданиях › статья по материалам конференции › Рецензирование
Biosorption of uranyl ion from radioactive solution. / Boguslavsky, Anatoliy; Yurkevich, Nataliya; Saeva, Olga и др.
в: International Multidisciplinary Scientific GeoConference Surveying Geology and Mining Ecology Management, SGEM, Том 17, № 52, 01.01.2017, стр. 113-120.Результаты исследований: Научные публикации в периодических изданиях › статья по материалам конференции › Рецензирование
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TY - JOUR
T1 - Biosorption of uranyl ion from radioactive solution
AU - Boguslavsky, Anatoliy
AU - Yurkevich, Nataliya
AU - Saeva, Olga
AU - Gaskova, Olga
PY - 2017/1/1
Y1 - 2017/1/1
N2 - U(VI) biosorption by six natural materials: three types of peats, Polytrichium moss, Eichhórnia crássipes water plant and Cladonia stellaris lichen was investigated. Natural sorbents were selected, as it is available, cheap and accessible materials. The effects of initial concentration of UO22- in the model radioactive solution and pH on the sorption uranyl ions were assessed. Adsorption isotherms and constants for given adsorbates and adsorbents were determined. Equilibrium is well described by Freundlich equation with the maximum biosorption capacity for Polytrichium moss as 70 mg/g after its interaction with UO2(NO3)2 solution (uranium initial concentration 959 mg/L, pH 4.4) during 24 hours. Our results reveal that peat is an efficient adsorbent for uranium that could be leached out from nuclear waste or U-containing rocks. One g/L of peat proved to be sufficient amount to remove contamination concentration of 0.3 mg/L U in contact time of 24 hours. IR spectroscopy allowed us to conclude that several functional groups in the organic compounds of examined sorbents participate in binding of the uranyl-ion: -CH, -COO, -COOH, -C=O. Therefore, the uranyl-ion bind with organic compounds of the peat and moss samples mainly due to the interaction of carboxyl group with uranyl-ions. The increased sorption in alkaline conditions and pH values decreased after experiments confirm the chemical sorption. However, the Freundlich adsorption isotherms and SEM mapping of the U species indicate surface adsorption also.
AB - U(VI) biosorption by six natural materials: three types of peats, Polytrichium moss, Eichhórnia crássipes water plant and Cladonia stellaris lichen was investigated. Natural sorbents were selected, as it is available, cheap and accessible materials. The effects of initial concentration of UO22- in the model radioactive solution and pH on the sorption uranyl ions were assessed. Adsorption isotherms and constants for given adsorbates and adsorbents were determined. Equilibrium is well described by Freundlich equation with the maximum biosorption capacity for Polytrichium moss as 70 mg/g after its interaction with UO2(NO3)2 solution (uranium initial concentration 959 mg/L, pH 4.4) during 24 hours. Our results reveal that peat is an efficient adsorbent for uranium that could be leached out from nuclear waste or U-containing rocks. One g/L of peat proved to be sufficient amount to remove contamination concentration of 0.3 mg/L U in contact time of 24 hours. IR spectroscopy allowed us to conclude that several functional groups in the organic compounds of examined sorbents participate in binding of the uranyl-ion: -CH, -COO, -COOH, -C=O. Therefore, the uranyl-ion bind with organic compounds of the peat and moss samples mainly due to the interaction of carboxyl group with uranyl-ions. The increased sorption in alkaline conditions and pH values decreased after experiments confirm the chemical sorption. However, the Freundlich adsorption isotherms and SEM mapping of the U species indicate surface adsorption also.
KW - Adsorption
KW - Biosorbtion
KW - Moss
KW - Peat
KW - Uranil solution
UR - http://www.scopus.com/inward/record.url?scp=85032364291&partnerID=8YFLogxK
U2 - 10.5593/sgem2017/52/S20.015
DO - 10.5593/sgem2017/52/S20.015
M3 - Conference article
AN - SCOPUS:85032364291
VL - 17
SP - 113
EP - 120
JO - International Multidisciplinary Scientific GeoConference Surveying Geology and Mining Ecology Management, SGEM
JF - International Multidisciplinary Scientific GeoConference Surveying Geology and Mining Ecology Management, SGEM
SN - 1314-2704
IS - 52
ER -
ID: 9872961