低温下碘化银与水溶液之间的边界层

B. Vincent, J. Lyklema
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引用次数: 16

摘要

在0-20°C的温度范围内,在LiNO3、KNO3和RbNO3的存在下,对AgI悬浮液进行了电位滴定研究。从滴定结果得出的零电荷点(p.z.c)、双层容量和表面熵数据表明,随着温度趋于0°C,在p.z.c区域周围,特别是在正侧,水的“结构”增加。对于带强负电荷的表面,偶极子上的电荷排序效应倾向于破坏这种结构。对AgI溶胶的絮凝研究结果与滴定数据相结合,得到了双层参数随温度变化的信息。结果与有关界面水结构变化的建议相吻合。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Boundary layers between silver iodide and aqueous solutions at low temperatures
Potentiometric titration studies have been made on AgI suspensions over the temperature range 0–20°C, in the presence of LiNO3, KNO3 and RbNO3. Points-of-zero-charge (p.z.c.), double-layer capacities and surface entropy data, derived from the titration results, indicate an increase in water “structure”, as the temperature tends to 0°C, around the p.z.c. region, and particularly on the positive side. For strongly negatively charged surfaces the charge ordering effect on the dipoles tends to break down this structuring. The results of flocculation studies on AgI sols have been combined with the titration data to yield information about changes in double layer parameters with temperature. The results fit the suggestions made regarding changes in water structuring at the interface.
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