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FeCl2-K2MoS4体系电催化还原乙炔为乙烯
引用本文:许书楷,张瀛州,周绍民.FeCl2-K2MoS4体系电催化还原乙炔为乙烯[J].应用化学,1987,0(2):42-45.
作者姓名:许书楷  张瀛州  周绍民
作者单位:1. 厦门大学化学系;2. 厦门大学物理化学研究所
摘    要:采用控电位电解、循环伏安法和交流阻抗法研究了FeCl2-K2MoS4体系对乙炔在石墨电极上还原为乙烯的电催化活性及反应机理。实验结果表明,当石墨阴极的电位控制在-1.50V(vs.SCE)时,FeCl2+K2MoS4的DMF溶液对C2H2还原为C2H4表现出明显的电催化活性和高的选择性。在-0.5~-1.0V时Mo(Ⅵ)还原为Mo(Ⅴ);在按连串的电子传递机理进行的Mo(Ⅴ)→Mo(Ⅲ)反应的电位区间(-1.0~-1.50V)溶液中所形成的络合品种传递电子的能力更强。Mo(Ⅲ)可能是络合物的电活性成分。

收稿时间:1986-01-21
修稿时间:1986-09-10

ELECTROCATALYTIC REDUCTION OF C2H2 TO C2H2 IN FERROUS-MOLYBDATE SYSTEMS
Xu Shukai,Zhang Yingzhou,Zhou Shaomin.ELECTROCATALYTIC REDUCTION OF C2H2 TO C2H2 IN FERROUS-MOLYBDATE SYSTEMS[J].Chinese Journal of Applied Chemistry,1987,0(2):42-45.
Authors:Xu Shukai  Zhang Yingzhou  Zhou Shaomin
Institution:1. Department of Chemistry, Xiamen University;2. Institute of Physical Chemistry, Xiamen University
Abstract:The electrochemical reduction of C2H2 to C2H4 in 0.1M NaClO4 DMF solution containing FeCl2 and K2MoS4 has been investigated by using potentiostatic electrolysis, cyclic voltammetry and a.c.impedance methods. The results showed that the ferrous-molybdate systems exhibited an appreciable electrocatalytic activity and high selectivity in reducing C2H2 to C2H4 when the potential of the graphite electrode was at -1.50V (vs.SCE). It was sugges-ted that the reaction Mo(Ⅵ)→Mo(Ⅴ) takes place at -0.5--1.0V and the reaction Mo(Ⅴ) to Mo(Ⅲ) at -1.0--1.5V,which proceeds through a consecutive electron transfer mechanism, forming a complex of Mo(Ⅲ) as electorcatalytically active species, faciliating the electron transfer of the reaction.
Keywords:
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