Simultaneous Phenol Removal and Resource Recovery from Phenolic Wastewater by Electrocatalytic Hydrogenation

被引:88
作者
Gu, Zhenao [1 ,2 ,3 ]
Zhang, Zhiyang [1 ]
Ni, Nan [1 ]
Hu, Chengzhi [1 ,2 ,3 ]
Qu, Jiuhui [1 ,2 ]
机构
[1] Chinese Acad Sci, Res Ctr Ecoenvironm Sci, State Key Lab Environm Aquat Chem, Beijing 100085, Peoples R China
[2] Univ Chinese Acad Sci, Beijing 100049, Peoples R China
[3] Natl Engn Res Ctr Ind Wastewater Detoxicat & Reso, Beijing 100085, Peoples R China
基金
国家重点研发计划; 中国国家自然科学基金;
关键词
  phenols; resource recovery; electrocatalytic hydrogenation; active sites; micro fl uidic channels; dechlorination; ADVANCED OXIDATION PROCESSES; REDUCTION; HYDRODEOXYGENATION; POLLUTANTS; CATHODE; PHASE; FUELS;
D O I
10.1021/acs.est.1c07457
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Efficient pollutants removal and simultaneous resource recovery from wastewater are of great significance for sustainable development. In this study, an electrocatalytic hydrogenation (ECH) approach was developed to selectively and rapidly transform phenol to cyclohexanol, which possesses high economic value and low toxicity and can be easily recovered from the aqueous solution. A three-dimensional Ru/TiO2 electrode with abundant active sites and massive microflow channels was prepared for efficient phenol transformation. A pseudo-first-order rate constant of 0.135 min-1 was observed for ECH of phenol (1 mM), which was 34-fold higher than that of traditional electrochemical oxidation (EO). Both direct electron transfer and indirect reduction by atomic hydrogen (H*) played pivotal roles in the hydrogenation of phenol ring. The ECH technique also showed excellent performance in a wide pH range of 3-11 and with a high concentration of phenol (10 mM). Moreover, the functional groups (e.g., chloro- and methyl-) on phenol showed little influence on the superiority of the ECH system. This work provides a novel and practical solution for remediation of phenolic wastewater as well as recovery of valuable organic compounds.
引用
收藏
页码:4356 / 4366
页数:11
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