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Formation of hydrate films on the surface of calcium silicate and aluminate in the presence of polyelectrolytes

机译:在聚电解质存在下在硅酸钙表面上形成水合物膜和铝酸盐

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摘要

To elucidate the mechanism of moistening and overmoistening of soils and mineral soil components capable of chemical hydration, the sorption of water vapor has been studied in combination with synchronous conductometric measurements. Effect of organic polyelectrolyte molecules on the hydration kinetics and the formation of hydrate films on their surface has been revealed for dehydrated calcium silicate and aluminate simulating minor soil components. The plotting of sorption-desorption curves has shown that hydrate-polymer films formed by aliphatic or aromatic polyelectrolytes with different functional groups (-COOH,-OH,-NH2,-CONH, etc.) significantly vary in dispersion and structure. The changes in dispersion during hydration are frequently not correlated with the amount of resulting hydrates, the content of which is controlled by the crystallochemical features of sorbents, the structure and activity of the polymer functional groups, and the conditions of sorption kinetic studies. It has been shown that the formation of low-permeable surface organomineral layers is typical for aliphatic polyelectrolytes, while more permeable layers determining the water-physical and structure-forming properties of soils are typical for aromatic polyelectrolytes.
机译:为了阐明能够化学水化的土壤和矿物土壤成分的润湿和过度造成的机理,已经研究了水蒸气的吸附与同步电导测量进行了研究。有机聚电解质分子对水合动力学的影响及其表面上水合物膜的形成,脱水硅酸钙和铝酸盐模拟小土壤成分。吸附解吸曲线的绘制已经表明,通过脂族或芳族聚电解质形成的水合物聚合物膜,其具有不同官能团(-COOH,-OH,-NH2,-CONH等)的分散体和结构显着变化。水合过程中的分散的变化通常与所得水合物的量不相关,其含量由吸附剂的结晶特征,聚合物官能团的结晶特征,以及化合物官能团的结构和活性的控制和吸附动力学研究的条件。已经表明,耐脂族聚电解质的低渗表面有机体层的形成是典型的,而确定芳族聚电解质的典型典型透渗透层的透明层是典型的。

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