Particle formation in the hydrolysis of tetraethyl orthosilicate in pH buffer solution

被引:47
作者
Nagao, D [1 ]
Osuzu, H [1 ]
Yamada, A [1 ]
Mine, E [1 ]
Kobayashi, Y [1 ]
Konno, M [1 ]
机构
[1] Tohoku Univ, Grad Sch Engn, Dept Chem Engn, Aoba Ku, Sendai, Miyagi 9808579, Japan
关键词
particle formation; hydrolysis; tetracthyl orthosilicate; pH buffer; silica particle; ammonia; methylanmine; dimethylainine; electrostatic interaction; zeta potential;
D O I
10.1016/j.jcis.2004.06.041
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
Particle formation in the hydrolysis and condensation of tetraethyl orthosilicate (TEOS) was studied by varying pH (9.5-11) with the basic catalysts NH3, methylamine (MA), and dimethylamine (DMA) in the presence of 5 mol/m(3) CH3COOH, which was chosen to suppress time variations of pH and ionic strength during the reaction. Spherical particles were formed for MA and DMA at catalyst concentrations of 0.02-0.2 kmol/m(3) and for NH3 at catalyst concentrations of 0.1-1.5 kmol/m(3). In a common range of catalyst concentrations for spherical particle formation, average particle size was largest for DMA and smallest for NH3. Hydrolysis rate of TEOS Could be quantified by the use of buffer systems as a function of TEOS and OH- concentrations. A specific relation was not found between the hydrolysis and the particle size. The zeta potential of silica particles measured in the reaction solvent was in the order DMA < MA < NH3, and ionic strength, estimated from pH in the reactions, was in the order DMA congruent to MA > NH3. This Suggested that the particle sizes were controlled by electrostatic particle interactions. (C) 2004 Elsevier Inc. All rights reserved.
引用
收藏
页码:143 / 149
页数:7
相关论文
共 20 条
[1]  
Blaaderen AV, 1992, J COLLOID INTERF SCI, V154, P481, DOI [10.1016/0021-9797(92)90163-G, DOI 10.1016/0021-9797(92)90163-G]
[2]   UNIFORM SILICA PARTICLE-PRECIPITATION - AN AGGREGATIVE GROWTH-MODEL [J].
BOGUSH, GH ;
ZUKOSKI, CF .
JOURNAL OF COLLOID AND INTERFACE SCIENCE, 1991, 142 (01) :19-34
[3]   CONTROLLED MICROCRYSTALLINE GROWTH-STUDIES BY DYNAMIC LASER-LIGHT-SCATTERING METHODS [J].
BYERS, CH ;
HARRIS, MT ;
WILLIAMS, DF .
INDUSTRIAL & ENGINEERING CHEMISTRY RESEARCH, 1987, 26 (09) :1916-1923
[4]   Kinetics of formation of monodisperse colloidal silica particles through the hydrolysis and condensation of tetraethylorthosilicate [J].
Chen, SL ;
Dong, P ;
Yang, GH ;
Yang, JJ .
INDUSTRIAL & ENGINEERING CHEMISTRY RESEARCH, 1996, 35 (12) :4487-4493
[5]   BACKGROUND ELECTROLYTE CORRECTION FOR ELECTROKINETIC SONIC AMPLITUDE MEASUREMENTS [J].
DESAI, FN ;
HAMMAD, HR ;
HAYES, KF .
LANGMUIR, 1993, 9 (11) :2888-2894
[6]  
GELSEMA WJ, 1966, RECL TRAV CHIM PAY-B, V85, P647
[7]   Size, volume fraction, and nucleation of Stober silica nanoparticles [J].
Green, DL ;
Lin, JS ;
Lam, YF ;
Hu, MZC ;
Schaefer, DW ;
Harris, MT .
JOURNAL OF COLLOID AND INTERFACE SCIENCE, 2003, 266 (02) :346-358
[8]   Effect of electrolyte additives on sol-precipitated nano silica particles [J].
Kim, SS ;
Kim, HS ;
Kim, SG ;
Kim, WS .
CERAMICS INTERNATIONAL, 2004, 30 (02) :171-175
[9]   Assessing extreme models of the Stober synthesis using transients under a range of initial composition [J].
Lee, K ;
Look, JL ;
Harris, MT ;
McCormick, AV .
JOURNAL OF COLLOID AND INTERFACE SCIENCE, 1997, 194 (01) :78-88
[10]   MONOMER-ADDITION GROWTH WITH A SLOW INITIATION STEP - A GROWTH-MODEL FOR SILICA PARTICLES FROM ALKOXIDES [J].
MATSOUKAS, T ;
GULARI, E .
JOURNAL OF COLLOID AND INTERFACE SCIENCE, 1989, 132 (01) :13-21