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基于原位红外光谱的水相苯酚电氧化机理研究

王家德 袁通斌 周丹飞 周栩乐 甘永平

化工学报2019,Vol.70Issue(12):4821-4827,7.
化工学报2019,Vol.70Issue(12):4821-4827,7.DOI:10.11949/0438-1157.20190689

基于原位红外光谱的水相苯酚电氧化机理研究

Mechanism of phenol electro-oxidation in aqueous solution based on in situ infrared spectroscopy

王家德 1袁通斌 1周丹飞 1周栩乐 1甘永平1

作者信息

  • 1. 浙江工业大学环境学院,浙江杭州310032
  • 折叠

摘要

Abstract

The electrochemical oxidation mechanism of phenol on the surface of Pt electrode was studied by electrochemical in situ spectroscopy. In 0.1 mol/L Na2SO4 solution, the reaction potential of electrochemical oxidation of phenol on Pt electrode is +0.9—1.0 V (vs SCE), and the oxygen evolution potential is +1.3 V. In situ infrared spectroscopy showed that electrode potential had a great influence on oxidation behavior of phenol. When the potential was lower than 0.9 V, the main intermediates of phenol oxidation were dihydroxyhenzene, quinone and a few alcohols. When the potential was controlled between 0.9 V and 1.1 V, the structure of benzene ring was destroyed, and the main intermediates were ketones, acids, alcohols and CO2. According to the changes in absorption peak of functional group, phenol oxidation on the platinum electrode surface was as follows: phenol, dihydroxyhenzene, quinone, ketone, alcohol, acid and CO2. The potential of ammonia oxidation on the platinum electrode surface was + 0.5 V, which indicated that ammonia in competition with phenol oxidation in the low potential region (<0.9 V).

关键词

苯酚/原位红外光谱/电化学氧化/界面/机理

Key words

phenol/ in situ FTIR/ electrochemical oxidation/ interface, mechanism

分类

数理科学

引用本文复制引用

王家德,袁通斌,周丹飞,周栩乐,甘永平..基于原位红外光谱的水相苯酚电氧化机理研究[J].化工学报,2019,70(12):4821-4827,7.

基金项目

国家自然科学基金项目(51878614) (51878614)

化工学报

OA北大核心CSCDCSTPCD

0438-1157

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