A. Diaz, D. Fenzel-Alexander, D. Miller, D. Wollmann, A. Eisenberg
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引用次数: 4
Abstract
Contract electrification measurements were performed on polymeric particles containing toluenesulfonate salt. Two forms of the toluenesulfonate ion pair were studied, an ionomer, poly(styrene-co-N-methyl-4-vinylpyridinium toluenesulfonate) and a molecular salt, cetyltrimethylammonium toluenesulfonate. Both types of particles charge positive, and the ionomer produces the higher charge level. XPS analysis shows that the particles containing the ionomer have a surface salt composition that resembles the formulation composition, whereas the surface salt composition of the particles containing the molecular is significantly higher than in the formulation. The variation in the surface ion concentration is used to estimate a relative charging capacity of the salts. XPS analyses of the carriers that were used with both particles shows an S 2p signal appropriate for the toluenesulfonate anion. A mechanism for charging involving the transfer of the toluenesulfonate anion from polymer particles to the carrier is proposed.
对含甲苯磺酸盐的聚合物颗粒进行了收缩电测量。研究了两种形式的甲苯磺酸离子对,一种是离子单体聚苯乙烯-co- n -甲基-4-乙烯基吡啶甲苯磺酸,另一种是分子盐十六烷基三甲基甲苯磺酸铵。两种类型的粒子都带正电荷,而离聚体产生更高的电荷水平。XPS分析表明,含有该离聚体的颗粒表面盐组成与配方组成相似,而含有该分子的颗粒表面盐组成明显高于配方。表面离子浓度的变化被用来估计盐的相对充电容量。对这两种粒子的载流子的XPS分析表明,存在适合于甲苯磺酸阴离子的s2p信号。提出了一种涉及甲苯磺酸阴离子从聚合物颗粒转移到载体的充电机制。