过硫酸盐
吸附
化学
催化作用
碳纳米管
甲醛
激进的
化学工程
催化氧化
光化学
无机化学
活性炭
有机化学
工程类
作者
Zhenhua Dai,Didi Li,Zhimin Ao,Shaobin Wang,Taicheng An
标识
DOI:10.1016/j.jhazmat.2020.124684
摘要
Carbon-catalyzed persulfate activation for the removal of gaseous volatile organic compounds (VOCs) has not been reported yet, and the corresponding fundamental mechanisms of VOCs adsorption and the subsequent VOCs degradation remain controversial. In this work, theoretical chemistry calculations were carried out to explore the VOCs removal mechanism by the persulfate-based advanced oxidation processes (P-AOPs) for VOCs removal over single walled carbon nanotubes (SWCNT). This study provided detailed theoretical insights into the SWCNT/P-AOPs for VOCs treatment in terms of adsorption, activation, mineralization, and diffusion of VOCs or peroxymonosulfate (PMS). Various VOCs were found to be preferentially adsorbed onto SWCNT, and the adsorption strength of VOCs was found to be significantly dependent on their polarizability. On the other side, PMS adsorbed on SWCNT could be efficiently activated through accepting π electron in the sp2 carbon matrix of SWCNT rather than the electrons at dangling bonds to generate •OH radicals attributed to the strong interaction between PMS and SWCNT. Formaldehyde was then taken as an example to evaluate the catalytic degradation pathways via SWCNT/P-AOPs. Under the attack of •OH radicals, the ultrafast degradation pathway of formaldehyde with no byproduct CO was identified with ultralow reaction energy barrier and large energy release. In addition, factors affecting the adsorption of organic compounds were identified and the detailed PMS activation pathway was present directly in this work. Above all, this work extended the carbons/P-AOPs system to VOCs abatement and presented systematic evidences for the essential mechanisms associated with VOCs adsorption and PMS activation by SWCNT, and the corresponding removal pathway and mechanism were also understood.
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