Geochemical constraints on the stability of zeolites and C-S-H in the high pH reaction of bentonite

被引:41
作者
Fernandez, Raul [1 ]
Rodriguez, Manuel [2 ]
Vigil de la Villa, Raquel [2 ]
Cuevas, Jaime [2 ]
机构
[1] CSIC, Inst Ciencias Construcc Eduardo Torroja, Madrid 28033, Spain
[2] Univ Autonoma Madrid, Fac Ciencias, Dpto Geol & Geoquim, E-28049 Madrid, Spain
关键词
UNDERGROUND LABORATORY FRANCE; 6 SYNTHETIC SAMPLES; COMPACTED BENTONITE; MONTMORILLONITE DISSOLUTION; THERMOCHEMICAL DATA; ALKALINE-SOLUTION; NATURAL ANALOG; OXFORDIAN CLAY; SILICATE; MINERALS;
D O I
10.1016/j.gca.2009.10.042
中图分类号
P3 [地球物理学]; P59 [地球化学];
学科分类号
0708 ; 070902 ;
摘要
Cement-bentonite interactions will occur in deep geological repositories for high level radioactive waste. We performed laboratory experiments in order to constrain some previous geochemical and mineralogical uncertainties in the formation of secondary minerals in the high pH reaction of FEBEX bentonite at moderate temperatures. The reactivity of a Mg-homoionic FEBEX bentonite was studied at 25, 60 and 90 degrees C in batch reactors using two solutions representative of short and long time evolution stages of cement degradation. These solutions were periodically renewed in order to maintain a constant pH regime for a period of almost 2 years. Chabazite and merlinoite were observed to be the main zeolites that formed at 60 degrees C, while merlinoite was the dominant zeolite formed at 90 degrees C with the hyperalkaline (K-Na-OH) solution. The alkaline experiments (Ca-OH solution) showed minor reactivity and negligible mineralogical alteration, but the overall results suggest that the reaction tends to equilibrium conditions between C-S-H and montmorillonite at high temperature and metastable conditions at low temperature. The montmorillonite dissolution rates were calculated for all experiments, showing good agreement with previous calculations. (C) 2009 Elsevier Ltd. All rights reserved.
引用
收藏
页码:890 / 906
页数:17
相关论文
共 62 条
[1]  
AIELLO R, 1968, REND ACAD SCI FIS N, V4, P1
[2]  
AKIZUKI M, 1989, AM MINERAL, V74, P1337
[3]   GROWTH TWINNING IN PHACOLITE [J].
AKIZUKI, M ;
KONNO, H .
MINERALOGICAL MAGAZINE, 1987, 51 (361) :427-430
[4]  
Appelo CAJ, 2004, GEOCHEMISTRY GROUNDW, DOI DOI 10.1201/9781
[5]   CHEMISTRY OF SOIL MINERALS .13. REACTIONS OF METAKAOLINITE WITH SINGLE AND MIXED BASES [J].
BARRER, RM ;
MAINWARING, DE .
JOURNAL OF THE CHEMICAL SOCIETY-DALTON TRANSACTIONS, 1972, (22) :2534-+
[6]  
BARTER RM, 1956, J CHEM SOC, P2882
[7]   Kaolinite and smectite dissolution rate in high molar KOH solutions at 35° and 80°C [J].
Bauer, A ;
Berger, G .
APPLIED GEOCHEMISTRY, 1998, 13 (07) :905-916
[8]  
BERNER U R, 1992, Waste Management, V12, P201, DOI 10.1016/0956-053X(92)90049-O
[9]  
Brindley G.W., 1980, CRYST STRUCT COMMUN, P125, DOI [10.1180/mono-5.2, DOI 10.1180/MONO-5]
[10]   Bentonites from Cabo de Gata, Almeria, Spain: a mineralogical and geochemical overview [J].
Caballero, E ;
De Cisneros, CJ ;
Huertas, FJ ;
Huertas, F ;
Pozzuoli, A ;
Linares, J .
CLAY MINERALS, 2005, 40 (04) :463-480