Influence of Iron Cations on Tetraethoxysilane Hydrolysis and Gelation Process

IF 1.4 4区 化学 Q4 CHEMISTRY, PHYSICAL
E. N. Titov, D. E. Smalchenko, O. E. Lebedeva
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Abstract

The influence of small additives of Fe3+ ions on tetraethoxysilane hydrolysis and subsequent polycondensation of products has been studied by the viscometry and dynamic light scattering methods. Experiments have been carried out at 50°C. Hydrolysis has been carried out at pH 1.5, 2.5, 5.0, or 7.0. The amount of the dopant cations has been varied from 1.5 to 3.8 at %. In the absence of the dopant cations, the gelation time grows with increasing pH from 1.5 to 5.0, while polycondensation occurs without gelation at pH 7.0. If the dopant is added at pH 1.5, the gelation time increases, but, at pH 2.5 and 5.0, it decreases. The gelation time increases with the dopant content at all three pH values. The size of the particles formed during the polycondensation process depends on the pH and the amount of the dopant. The smallest particles with a median diameter of about 10 nm are formed at pH 2.5. It is assumed that the cause of all observed effects is the incorporation of iron cations into the siloxane matrix. The degree of the incorporation depends on the degree of iron cation hydrolysis. This assumption is confirmed by the values of the electrokinetic potential of the studied systems and the dynamics of variations in the zeta-potential with varying pH and dopant content.

Abstract Image

铁阳离子对四乙氧基硅烷水解和凝胶化过程的影响
采用粘度法和动态光散射法研究了微量Fe3+离子添加剂对四乙氧基硅烷水解及缩聚产物的影响。实验在50℃下进行。水解已在pH 1.5, 2.5, 5.0或7.0进行。掺杂阳离子的含量在1.5% ~ 3.8%之间变化。在没有掺杂阳离子的情况下,随着pH从1.5到5.0的增加,凝胶时间增加,而在pH 7.0时,没有凝胶的缩聚发生。在pH为1.5时,掺杂剂的凝胶时间增加,而在pH为2.5和5.0时,掺杂剂的凝胶时间减少。在三种pH值下,凝胶时间随掺杂剂含量的增加而增加。缩聚过程中形成的颗粒大小取决于pH值和掺杂量。pH值为2.5时形成的最小颗粒中位直径约为10 nm。假定所有观察到的效应的原因是铁阳离子掺入硅氧烷基体。掺入的程度取决于铁阳离子水解的程度。这一假设被所研究体系的电动势值和ζ电位随pH和掺杂物含量变化的动力学变化所证实。
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来源期刊
Colloid Journal
Colloid Journal 化学-物理化学
CiteScore
2.20
自引率
18.20%
发文量
36
审稿时长
6-12 weeks
期刊介绍: Colloid Journal (Kolloidnyi Zhurnal) is the only journal in Russia that publishes the results of research in the area of chemical science dealing with the disperse state of matter and surface phenomena in disperse systems. The journal covers experimental and theoretical works on a great variety of colloid and surface phenomena: the structure and properties of interfaces; adsorption phenomena and structure of adsorption layers of surfactants; capillary phenomena; wetting films; wetting and spreading; and detergency. The formation of colloid systems, their molecular-kinetic and optical properties, surface forces, interaction of colloidal particles, stabilization, and criteria of stability loss of different disperse systems (lyosols and aerosols, suspensions, emulsions, foams, and micellar systems) are also topics of the journal. Colloid Journal also includes the phenomena of electro- and diffusiophoresis, electro- and thermoosmosis, and capillary and reverse osmosis, i.e., phenomena dealing with the existence of diffusion layers of molecules and ions in the vicinity of the interface.
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