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首页> 外文期刊>The journal of physical chemistry, B. Condensed matter, materials, surfaces, interfaces & biophysical >Mechanism of Solid/Liquid Interfacial Reactions. Atomic Force Microscopy Studies of the Self-Passivating Reaction between Solid p-Chloranil and Aqueous Phase N,N-Dimethylphenylenediamine
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Mechanism of Solid/Liquid Interfacial Reactions. Atomic Force Microscopy Studies of the Self-Passivating Reaction between Solid p-Chloranil and Aqueous Phase N,N-Dimethylphenylenediamine

机译:固/液界面反应的机理。固体对氯腈与水相N,N-二甲基苯二胺之间自钝化反应的原子力显微镜研究

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摘要

The reaction between solid p-chloranil and alkaline aqueous solutions of dimethylphenylenediamine is shown to be self-passivating owing to the formation of insoluble product at the reacting interface. In situ atomic force microscopy imaging of the reaction occurring at (010) surfaces of single crystals of p-chloranil show that the nucleation of the overgrowth is progressive and that its coverage, S, follows the time (t) dependence S(t) = 1 - exp(-k_3t~3), where k_3 is a rate constant. Measurement of the z piezo voltage throughout the reaction to give an absolute measure of the surface heigh shows that appreciable (hydroxide driven) dissolution occurs prior to the formation of the overgrowth and the surface becoming fully passivated.
机译:由于在反应界面上形成不溶性产物,固体对氯苯胺与二甲基苯二胺的碱性水溶液之间的反应显示为自钝化。对氯苯胺单晶的(010)表面发生的反应的原位原子力显微镜成像显示,过度生长的成核是渐进的,其覆盖率S遵循时间(t)依赖性S(t)= 1-exp(-k_3t〜3),其中k_3是速率常数。在整个反应过程中对z压电电压进行测量以给出表面高度的绝对值,这表明在形成过度生长和表面完全钝化之前,发生了明显的(氢氧化物驱动)溶解。

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