Rate of access to the binding sites in organically modified silicates.: 1.: Amorphous silica gels grafted with amine or thiol groups

被引:148
作者
Walcarius, A [1 ]
Etienne, M [1 ]
Bessière, J [1 ]
机构
[1] Univ Nancy 1, Lab Chim Phys & Microbiol Environm, UMR 7564, CNRS, F-54600 Villers Les Nancy, France
关键词
D O I
10.1021/cm021117k
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 speed at which selected reactants are reaching active sites grafted on porous silica gels of various nature and porosity was evaluated using some model systems: protonation of aminopropyl-grafted silica (APS), mercury(II) binding on mercaptopropyl-grafted silica (MPS), and accumulation of copper(II) on APS. Data were obtained from batch experiments, by monitoring the consumption of reactant in solutions containing the solid phases as dispersed particles (average size: 60-150 mum). Various grafted solids were studied, with pore diameter ranging between 4 and 15 nm and organic group contents of typically 1.4-1.9 mmol g(-1). Diffusion processes in the porous organically modified silicas were found to be dramatically restricted as compared to those observed in homogeneous solution (approximate to10(3)-10(4) times slower). They were dependent on several factors such as the pore size of the material and the size of the reactant, the density of grafted organic sites, and the nature of the starting silica gel. Evaluation of apparent diffusion coefficients was achieved by applying a simplified model based on spherical diffusion. This has allowed us to point out a significant decrease in the access rates upon gradual completion of reactions: as the reactant concentration in the vicinity of increasing amounts of grafted groups is raised progressively, there is less room available in the porous structure to enable the probe to reach rapidly the remaining active sites. The apparent diffusion coefficient was found to drop dramatically after typically 30-50% reaction completion, depending on the nature of the probe. This study allows highlighting the optimal conditions that should be required to ensure efficient application of grafted silica gels, that is, in the fields of catalysis or heavy metal extraction.
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页码:2757 / 2766
页数:10
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共 130 条
[71]   Durable modification of silica aerogel monoliths with fluorescent 2,7-diazapyrenium moieties. Sensing oxygen near the speed of open-air diffusion [J].
Leventis, N ;
Elder, IA ;
Rolison, DR ;
Anderson, ML ;
Merzbacher, CI .
CHEMISTRY OF MATERIALS, 1999, 11 (10) :2837-2845
[72]   PRECONCENTRATION OF TRACE-METALS USING CHELATING GROUPS IMMOBILIZED VIA SILYLATION [J].
LEYDEN, DE ;
LUTTRELL, GH .
ANALYTICAL CHEMISTRY, 1975, 47 (09) :1612-1617
[73]  
LEYDEN DE, 1976, ANAL CHIM ACTA, V84, P97
[74]   Comparative studies of grafting and direct syntheses of inorganic-organic hybrid mesoporous materials [J].
Lim, MH ;
Stein, A .
CHEMISTRY OF MATERIALS, 1999, 11 (11) :3285-3295
[75]   Synthesis of ordered microporous silicates with organosulfur surface groups and their applications as solid acid catalysts [J].
Lim, MH ;
Blanford, CF ;
Stein, A .
CHEMISTRY OF MATERIALS, 1998, 10 (02) :467-+
[76]   STUDIES ON PORE SYSTEMS IN CATALYSTS .V. T METHOD [J].
LIPPENS, BC ;
DEBOER, JH .
JOURNAL OF CATALYSIS, 1965, 4 (03) :319-&
[77]   A new class of hybrid mesoporous materials with functionalized organic monolayers for selective adsorption of heavy metal ions [J].
Liu, AM ;
Hidajat, K ;
Kawi, S ;
Zhao, DY .
CHEMICAL COMMUNICATIONS, 2000, (13) :1145-1146
[78]   Sol-gel processes [J].
Livage, J .
CURRENT OPINION IN SOLID STATE & MATERIALS SCIENCE, 1997, 2 (02) :132-138
[79]   BRIDGED POLYSILSESQUIOXANES - HIGHLY POROUS HYBRID ORGANIC-INORGANIC MATERIALS [J].
LOY, DA ;
SHEA, KJ .
CHEMICAL REVIEWS, 1995, 95 (05) :1431-1442
[80]   Preconcentration, separation and determination of trace Hg(II) in environmental samples with aminopropylbenzoylazo-2-mercaptobenzothiazole bonded to silica gel [J].
Ma, WX ;
Liu, F ;
Li, KA ;
Chen, M ;
Tong, SY .
ANALYTICA CHIMICA ACTA, 2000, 416 (02) :191-196