催化作用
煅烧
层状双氢氧化物
臭氧
化学
钴
苯胺
无机化学
化学工程
有机化学
工程类
作者
Yuanfeng Qi,Ce Guo,Xing Xu,Baoyu Gao,Qinyan Yue,Bo Jiang,Zhou Qian,Changzhi Wang,Yanqing Zhang
标识
DOI:10.1016/j.scitotenv.2020.136982
摘要
In this work, Co/Fe and Co/Al layered double oxides (Co/Fe-LDO and Co/Al- LDO)ozone catalysts were obtained from Co/Fe and Co/Al layered double hydroxides intermediates (Co/Fe-LDH and Co/Al-LDH). Firstly, the optimal preparation parameters of the two intermediates were determined, then the morphology and mineralogy microstructure of the derived Co/Fe-LDO and Co/Al- LDO ozone catalysts were systematically studied. Finally, the reaction kinetics of the two ozone catalysts for the deep degradation of aniline wastewater in catalysts/ozone systems were established. The results showed that the optimal preparation conditions were set as pH 12, temperature 60 °C, cobalt‑iron ratio 3:1 for Co/Fe-LDH intermediate, and pH 12, temperature 70 °C, cobalt‑aluminum ratio 3:1 for Co/Al-LDH intermediate. During calcination treatment, the dehydration and recrystallization effect impelled LDH intermediate to form LDO catalyst. The derived ozone catalysts Co/Fe-LDO and Co/Al-LDO possess layered structure, and Co species was mainly based on Co3O4 as the main mineral phase of the two ozone catalysts. The addition of catalyst can realize the deep ozonation catalysis of aniline wastewater. The kinetic models established on the aniline oxidized by ozone or catalyst/ozone systems were both fitted the first-order reactions, and the reaction activation energy for CODCr and TOC degradation were significantly reduced in catalyst/ozone system.
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