Kinetic study on the formation of colloidal gold in the presence of acetylenic glycol nonionic surfactant

被引:20
|
作者
Sato, S [1 ]
Toda, K [1 ]
Oniki, S [1 ]
机构
[1] Nagoya City Univ, Fac Pharmaceut Sci, Mizuho Ku, Nagoya, Aichi 4678603, Japan
关键词
kinetics; colloidal gold; Surfynol; 465; acetylenic glycol nonionic surfactant; monomer; micelle; activation energies;
D O I
10.1006/jcis.1999.6443
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 formation of colloidal gold was kinetically studied using the monomer or micelle form of the acetylenic glycol nonionic surfactant Surfynol 465, which functions as a reducing and stabilizing agent. When two equal volumes of aqueous solution of Au(III) and Surfynol 465 were mixed, absorbance at the peak around 300 nm due to Au(III) rapidly decreased with time exponentially. A new peak began to appear around 530 nm, whose height sigmoidally increased with time, showing the formation of colloidal gold. From the variation in absorbance at 300 or 530 nm with time, colloidal gold formation would appear to occur through consecutive first-order reactions, Au(III) --> Au(I) --> Au(0) --> gold particle, for monomer and micelle systems. As for Au(I), the complex between Au(I) and -C=C- of Surfynol 465 was assigned based on reactions previously proposed for the Raman spectra of colloidal gold (Sato, S., Colloid Polym. Sci. 274, 1161 (1996)). The reaction, Au(0) --> gold particle, proceeded quickly. The overall rate of reaction was slower in the micelle system than in the monomer system. For both systems, the rate constant of the reaction Au(III) --> Au(I) exceeded the constant of the reaction Au(I) --> Au(0), and the activation energies of the two reactions were 58 kJ mol(-1). From the agreement with the activation energy of formation of colloidal gold by another method, consecutive first-order reactions, Au(III) --> Au(I) --> Au(0) --> gold particle, were considered valid for the formation of colloidal gold in the presence of Surfynol 465. (C) 1999 Academic Press.
引用
收藏
页码:504 / 510
页数:7
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