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Sorption of cesium, strontium, and yttrium radionuclides from the aqueous phase on layered double hydroxides
Sorption of 137 Cs, 85,90 Sr, and 90 Y from aqueous solutions on the solid phase of layered double hydroxides (LDHs) and layered double oxides (LDOs) of various compositions was studied. On the solid phase of Mg-Al and Cu-Al LDHs and Mg-Al LDO, the Sr and Cs radionuclides are very weakly sorbed from...
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Published in: | Radiochemistry (New York, N.Y.) N.Y.), 2008-10, Vol.50 (5), p.493-501 |
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Main Authors: | , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | Sorption of
137
Cs,
85,90
Sr, and
90
Y from aqueous solutions on the solid phase of layered double hydroxides (LDHs) and layered double oxides (LDOs) of various compositions was studied. On the solid phase of Mg-Al and Cu-Al LDHs and Mg-Al LDO, the Sr and Cs radionuclides are very weakly sorbed from aqueous solutions containing 10
−5
M of the corresponding element (Cs
+
or Sr
2+
). Introduction of EDTA ions into Mg-Al LDH increases the distribution coefficients
K
d
of Sr by a factor of more than 40. After 96-h contact of the solid and liquid phases,
K
d
of radioactive Sr in sorption from aqueous solution on Mg-Al LDH and Mg-Al LDH-EDTA is 2.4 and 100 ml g
−1
, respectively. The Sr and Y radionuclides are efficiently sorbed from aqueous solutions containing 10
−5
M Sr
2+
and Y
3+
on the Mg-Nd LDH solid phase. After 5-min contact of the solid and liquid phases,
K
d
of Sr exceeds 10
5
ml g
−1
. For Y, the distribution coefficients equal to 700–800 ml g
−1
are attained after 30-min contact of the solid and liquid phases. Aging of the Mg-Nd LDH precipitate does not affect its sorption properties toward Sr and Y radionuclides. With an increase in the Sr(NO
3
)
2
concentration in the solution from 10
−5
to 10
−1
M, the distribution coefficients
K
d
z of Sr drastically decrease (virtually to zero) and those of Y change insignificantly. |
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ISSN: | 1066-3622 1608-3288 |
DOI: | 10.1134/S1066362208050111 |