Reactivity of basal surfaces, steps and edges of muscovite: An AFM study

被引:14
作者
Zhang, ZZ
Bailey, GW
机构
[1] US EPA, Natl Res Council, Athens, GA 30605 USA
[2] US EPA, Natl Exposure Res Lab, Ecosyst Res Div, Athens, GA 30605 USA
关键词
AFM; morphology; muscovite; precipitation; reactivity; surfaces;
D O I
10.1346/CCMN.1998.0460308
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 reactivity of basal surfaces, steps and edges of muscovite was studied by imaging surface precipitates of PbCl(2) using atomic force microscopy (AFM). We reacted PbCl(2) solution with freshly cleaved muscovite surfaces and found that PbCl(2) precipitates were formed on the basal surfaces, steps and edges. It was observed that PbCl(2) precipitated preferentially along the steps compared to the basal surfaces and that PbCl(2) precipitates at multiple-layer edges were needle-shaped and oriented in different directions. One of the muscovite samples we cleaved had muscovite fragments sitting on the freshly cleaved surfaces. These fragments resulted from previously formed cracks. Thus, we were able to compare the reactivity of the weathered surfaces with that of freshly cleaved surfaces. It was found that PbCl(2) was not precipitated along the edges of previously cracked muscovite fragments. These results clearly demonstrated that the edges of freshly cleaved muscovite are the most reactive surface sites, whereas the edges of weathered muscovite are not as reactive. We believe that the surface reactivity of the edges of freshly cleaved muscovite is likely due to terminal Al-OH(2)(1/2+) or Al-OH(1/2-) groups on these crystalline surfaces, which favor adsorption of Pb(2+) ions and the subsequent nucleation and precipitation reactions. We also investigated the effect of drying rate on the morphology of the surface precipitates. Fast drying resulted in a nearly complete covered surface with a leaflike morphology, whereas slow drying resulted in more isolated surface clusters.
引用
收藏
页码:290 / 300
页数:11
相关论文
共 30 条
[1]  
Allison J.D., 1991, MINTEQA2PRODEFA2 GEO
[2]  
[Anonymous], ENV CHEM ALUMINUM
[3]  
[Anonymous], 1988, ADV INORG CHEM
[4]   ATOMIC FORCE MICROSCOPE [J].
BINNIG, G ;
QUATE, CF ;
GERBER, C .
PHYSICAL REVIEW LETTERS, 1986, 56 (09) :930-933
[5]   FORCE MICROSCOPY [J].
BINNIG, G .
ULTRAMICROSCOPY, 1992, 42 :7-15
[6]   CLUSTER FORMATION VERSUS ISOLATED-SITE ADSORPTION - A STUDY OF MN(II) AND MG(II) ADSORPTION ON BOEHMITE AND GOETHITE [J].
BLEAM, WF ;
MCBRIDE, MB .
JOURNAL OF COLLOID AND INTERFACE SCIENCE, 1985, 103 (01) :124-132
[7]   IN-SITU INVESTIGATION OF GROWTH AND DISSOLUTION ON THE (010) SURFACE OF GYPSUM BY SCANNING FORCE MICROSCOPY [J].
BOSBACH, D ;
RAMMENSEE, W .
GEOCHIMICA ET COSMOCHIMICA ACTA, 1994, 58 (02) :843-849
[8]   NUCLEATION AND GROWTH OF FE ON CU(111) IN THE MONOLAYER RANGE [J].
BRODDE, A ;
NEDDERMEYER, H .
ULTRAMICROSCOPY, 1992, 42 :556-561
[9]   NONEQUILIBRIUM WATER-ROCK INTERACTIONS .1. MODEL FOR INTERFACE-CONTROLLED REACTIONS [J].
DIBBLE, WE ;
TILLER, WA .
GEOCHIMICA ET COSMOCHIMICA ACTA, 1981, 45 (01) :79-92
[10]   CALCITE PRECIPITATION MECHANISMS AND INHIBITION BY ORTHOPHOSPHATE - INSITU OBSERVATIONS BY SCANNING FORCE MICROSCOPY [J].
DOVE, PM ;
HOCHELLA, MF .
GEOCHIMICA ET COSMOCHIMICA ACTA, 1993, 57 (03) :705-714