Formation and release of cobalt(II) sorption and precipitation products in aging kaolinite-water slurries

被引:31
作者
Thompson, HA
Parks, GA
Brown, GE
机构
[1] Stanford Univ, Dept Geol & Environm Sci, Stanford, CA 94305 USA
[2] Stanford Synchrotron Radiat Lab, Stanford, CA 94309 USA
基金
美国国家卫生研究院; 美国国家科学基金会;
关键词
adsorption; aging; desorption; dissolution; EXAFS; hydrotalcite; precipitation; ripening; solid solution; stability;
D O I
10.1006/jcis.1999.6631
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
The uptake and release behavior of cobalt(II) was studied over thousands of hours in CO2-free aqueous suspensions of kaolinite under three pairs of total cobalt concentration (Co-T) and near-neutral pH (7.5-7.8) conditions. Dissolved cobalt, aluminum, and silicon concentrations were monitored by ICPMS, and cobalt-containing products were identified by EXAFS spectroscopy. In each uptake experiment, cobalt sorbed to kaolinite as a mixture of surface-adsorbed monomers or polymers and hydrotalcite-like precipitates of the approximate composition CoxAl(OH)(2x+2)(A(n-))(1/n), where 2 less than or equal to x less than or equal to 4 and A(n-) is nitrate or silicate anion, Precipitate stoichiometry varied with experimental conditions, with the highest Co:Al ratio in the high Co-T/high pH experiment. Cobalt surface adsorption occurred within seconds, whereas precipitation was slower and continued for the duration of the experiments. Consequently, the proportion of precipitate in the sorbed mixture increased with time in all experiments. The most rapid precipitation occurred in the high Co-T/high pH experiment, where solutions were most supersaturated with respect to cobalt hydrotalcite. Precipitates incorporated some previously adsorbed cobalt, as well as cobalt from solution. Cobalt release from the solid phase was effected by lowering solution pH to 7.0. Release experiments initiated after shorter sorption times returned a larger fraction of cobalt to solution than those initiated after longer sorption times, for a fixed duration of release. In other words, sorption product stability increased with sorption time. Specifically, under the conditions of the release experiments, the hydrotalcite-like precipitates are more stable than smaller adsorbates, and precipitates that formed over longer time periods are more stable than those that formed rapidly. The latter result suggests that precipitates ripened or modified their structure or composition to become more stable over the course of the several-thousand-hour sorption experiments. Precipitates that formed over hundreds of hours or longer did not dissolve over thousands of hours at the lower pH. (C) 2000 Academic Press.
引用
收藏
页码:241 / 253
页数:13
相关论文
共 34 条
[1]  
BANGASH M A, 1992, Waste Management, V12, P29, DOI 10.1016/0956-053X(92)90006-5
[2]   Outer-sphere Pb(II) adsorbed at specific surface sites on single crystal alpha-alumina [J].
Bargar, JR ;
Towle, SN ;
Brown, GE ;
Parks, GA .
GEOCHIMICA ET COSMOCHIMICA ACTA, 1996, 60 (18) :3541-3547
[3]  
BISH DL, 1980, B MINERAL, V103, P170
[4]   A SURFACE COMPLEX-REACTION MODEL FOR THE PH-DEPENDENCE OF CORUNDUM AND KAOLINITE DISSOLUTION RATES [J].
CARROLLWEBB, SA ;
WALTHER, JV .
GEOCHIMICA ET COSMOCHIMICA ACTA, 1988, 52 (11) :2609-2623
[5]   HYDROTALCITE-TYPE ANIONIC CLAYS: PREPARATION, PROPERTIES AND APPLICATIONS [J].
Cavani, F. ;
Trifiro, F. ;
Vaccari, A. .
CATALYSIS TODAY, 1991, 11 (02) :173-301
[6]   EVIDENCE FOR MULTINUCLEAR METAL-ION COMPLEXES AT SOLID WATER INTERFACES FROM X-RAY ABSORPTION-SPECTROSCOPY [J].
CHISHOLMBRAUSE, CJ ;
ODAY, PA ;
BROWN, GE ;
PARKS, GA .
NATURE, 1990, 348 (6301) :528-531
[7]  
DELACAILLERIE JBD, 1995, J AM CHEM SOC, V117, P11471
[8]   EFFECTS OF NONREVERSIBILITY, PARTICLE CONCENTRATION, AND IONIC-STRENGTH ON HEAVY-METAL SORPTION [J].
DITORO, DM ;
MAHONY, JD ;
KIRCHGRABER, PR ;
OBYRNE, AL ;
PASQUALE, LR ;
PICCIRILLI, DC .
ENVIRONMENTAL SCIENCE & TECHNOLOGY, 1986, 20 (01) :55-61
[9]   THE SOLUBILITY OF COBALT HYDROXIDE, CO(OH)2, IN SOLUTIONS OF HYDROCHLORIC ACID AND SODIUM HYDROXIDE AT 25 DEGREES [J].
GAYER, KH ;
GARRETT, AB .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1950, 72 (09) :3921-3923
[10]  
George G., 1995, EXAFSPAK: A suite of computer programs for analysis of X-ray absorption spectra