Interaction between Lu cations and 2:1 alumino silicates under hydrothermal treatment

被引:15
作者
Alba, MD [1 ]
Chain, P [1 ]
机构
[1] Univ Sevilla, CSIC, Dept Quim Inorgan, Inst Ciencia Mat Sevilla, Seville 41092, Spain
关键词
bentonite; CEC; hydrothermal alteration; lutetium cations; nuclear waste barriers; radionuclide barriers;
D O I
10.1346/CCMN.2005.0530105
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Smectites are considered to be an important component in backfill barriers due to their marked swelling and high cation exchange capacity. Both properties are affected considerably when these clays transform under natural conditions. However, we have recently described a chemical interaction between high-activity radionuclide simulators and smectites which could prove to be effective at immobilizing radionuclides definitively. Investigating the efficiency of this mechanism, independent of bentonite ageing, is a challenge. For this purpose, the reactivity shown by a non-expandable layered aluminosilicate, muscovite, has been compared to that shown by an expandable one, beidellite. Both samples were treated hydrothermally with a solution of lutetium nitrate, and the transformations were studied by X-ray diffraction, nuclear magnetic resonance and scanning electron microscopy/energy dispersive X-ray analysis. Lutetium cations react with the silicon framework of both 2:1 layered aluminosilicates under hydrothermal conditions, and new phases, lutetium disilicate, kaolinite, boehmite and natrosilite are generated. The results demonstrate that the efficiency of the chemical mechanism is not determined by the swelling and the cation exchange capacity of 2:1 layered aluminosilicates. Thus, the rare earth disilicate formation might account for the success of the clay barrier, once bentonite has lost its swelling and cation exchange capacity.
引用
收藏
页码:37 / 44
页数:8
相关论文
共 37 条
[1]  
Alba MD, 2001, AM MINERAL, V86, P115
[2]  
Allen C.C., 1988, APPL CLAY SCI, V3, P11, DOI [10.1016/0169-1317(88)90003-8, DOI 10.1016/0169-1317(88)90003-8]
[3]   SORPTION OF TRACE CONSTITUENTS FROM AQUEOUS-SOLUTIONS ONTO SECONDARY MINERALS .1. URANIUM [J].
AMES, LL ;
MCGARRAH, JE ;
WALKER, BA .
CLAYS AND CLAY MINERALS, 1983, 31 (05) :321-334
[4]   SORPTION OF URANIUM AND CESIUM BY HANFORD BASALTS AND ASSOCIATED SECONDARY SMECTITE [J].
AMES, LL ;
MCGARRAH, JE ;
WALKER, BA ;
SALTER, PF .
CHEMICAL GEOLOGY, 1982, 35 (3-4) :205-225
[5]  
Bailey S. W., 1980, CRYSTAL STRUCTURES C, P1, DOI [10.1180/mono-5, DOI 10.1180/MONO-5.1]
[6]   Smectite stability in acid salt solutions and the fate of Eu, Th and U in solution [J].
Bauer, A ;
Schäfer, T ;
Dohrmann, R ;
Hoffmann, H ;
Kim, JI .
CLAY MINERALS, 2001, 36 (01) :93-103
[7]  
BECERRO AI, 1997, THESIS U SEVILLE
[8]   THE ADSORPTION OF URANYL SPECIES BY FINE CLAY [J].
BOROVEC, Z .
CHEMICAL GEOLOGY, 1981, 32 (1-2) :45-58
[9]   SPECIATION OF URANYL SORBED AT MULTIPLE BINDING-SITES ON MONTMORILLONITE [J].
CHISHOLMBRAUSE, C ;
CONRADSON, SD ;
BUSCHER, CT ;
ELLER, PG ;
MORRIS, DE .
GEOCHIMICA ET COSMOCHIMICA ACTA, 1994, 58 (17) :3625-3631
[10]   Experimental kinetic study of the smectite-to-illite transformation [J].
Cuadros, J ;
Linares, J .
GEOCHIMICA ET COSMOCHIMICA ACTA, 1996, 60 (03) :439-453