Biosorption of long-lived radionuclides

被引:2
作者
Lyalikova-Medvedeva, NN [1 ]
Khijniak, TV [1 ]
机构
[1] Russian Acad Sci, Lab Ecol & Geochem Act Microorganisms, Inst Microbiol, Moscow 117811, Russia
来源
BIOHYDROMETALLURGY AND THE ENVIRONMENT TOWARD THE MINING OF THE 21ST CENTURY, PT B 1999 | 1999年 / 9卷
关键词
D O I
10.1016/S1572-4409(99)80122-9
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The aim of our work was to study the possibility to reduce the volume of radioactive wastes, using the sorption of radioactive elements by biomass or transfer in less soluble state. We dealt with technetium-99 (half-life is 2.12*10(5) y, specific activity - 1.7 mCi/ mmol). The fungi Aspergillus niger, Scopulariopsis brevicaulis, yeasts, several species of Pseudomonas, thionic and sulfate-reducing bacteria were used in the experiments. The radioactivity of solution (Tc - 24 mg/l) was decreased on 58, 65 and 40% after contact with A, niger, S. brevicaulis and yeast Pichia wicker, respectively. Anaerobic consortium of chromate-reducing bacteria removed technetium-99 almost completely. The concentration factor was 4,1*10(3). In experiments with sulfate-reducing bacteria the radioactivity was decreased on 25-48%. Sulfides of technetium Tc2S7 and TcS2 were formed. Vanadate-reducing bacteria decreased the radioactivity on 25% (concentration of Tc - 40 mg/l). The sorption by living cells was 4-5 times higher than by dead biomass. Thionic bacteria - Thiobacillus ferrooxidans and Thiobacillus thiooxidans can oxidize ferrous iron and sulfur in anaerobic conditions, using pertechnetate as electron acceptor. The decrease of radioactivity was 50-70%. By paper chromatography we shown that heptavalent technetium reduced to 4 and 5 valent states by cultures Pseudomonas vanadiumreductans in neutral conditions and thionic bacteria in acid media. Dead biomass of A. niger - a waste of citric acid plant was used in experiments for removing U, Am, Ce, Cs, Eu, Pa, Sb at joint presence. All elements were removed in different degree, which depends on their chemical properties and concentration.
引用
收藏
页码:327 / 334
页数:8
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[21]   FORMATION OF LONG-LIVED RADIONUCLIDES IN THE DEUTERON IRRADIATION OF ZIRCONIUM [J].
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