School of Environmental Science and Engineering, Tianjin University/Tianjin Key Lab of Biomass/Wastes Utilization, Tianjin 300072, PR China.
School of Environmental Science and Engineering, Tianjin University/Tianjin Key Lab of Biomass/Wastes Utilization, Tianjin 300072, PR China.
J Hazard Mater. 2022 Aug 15;436:129217. doi: 10.1016/j.jhazmat.2022.129217. Epub 2022 May 24.
This paper firstly reported efficient catalytic ozonation of CHCl (dichloromethane, DCM) at low temperature over hollow urchin-like MnO with high chlorine resistance. Regulations on morphologies and Cu doping, as well as ozone promotion were conducted to optimize active oxygen of MnO catalysts, contributing to excellent catalytic behaviors. Cu doping MnO with hollow urchin-like morphology attained a stable 100% DCM conversion with O/DCM molar ratio of 10 at 120 °C. The ozone utilization rate, final products, and byproducts distribution were discussed. Abundant crystal defects, low-valance Mn/Cu, O, and weak acidity, as well as better low temperature reducibility contributed to its superior performance. During DCM catalytic ozonation, DCM oxidation exhibited competitive effect on O decomposition due to the occupation of intermediates (CHClO·, O-CHCl, and O-CH -O) over active sites that should belong to O originally. Nevertheless, O decomposition exhibited synergistic effects on DCM oxidation with promotion on active oxygen. Density functional theory (DFT) calculations confirmed the positive effect on oxygen vacancy formation and O/DCM adsorption from Cu doping. The possible mechanism for DCM catalytic ozonation included four parts, including O/DCM adsorption, O activation, DCM oxidation, and electron replenishment. This paper provides new insight for catalytic elimination of chlorinated alkanes at mild conditions.
本文首次报道了在具有高耐氯性的中空海胆状 MnO 上低温高效催化臭氧氧化 CHCl(二氯甲烷,DCM)。通过调节形貌和 Cu 掺杂以及促进臭氧,优化了 MnO 催化剂的活性氧,从而表现出优异的催化性能。中空海胆状形貌的 Cu 掺杂 MnO 在 120°C 下,O/DCM 摩尔比为 10 时,可稳定达到 100%的 DCM 转化率。讨论了臭氧利用率、最终产物和副产物分布。丰富的晶体缺陷、低价态的 Mn/Cu、O 和弱酸性以及更好的低温还原性是其性能优异的原因。在 DCM 催化臭氧化过程中,由于中间体(CHClO·、O-CHCl 和 O-CH -O)占据了原本属于 O 的活性位,DCM 氧化对 O 分解表现出竞争效应。然而,O 分解对 DCM 氧化表现出协同效应,促进了活性氧的产生。密度泛函理论(DFT)计算证实了 Cu 掺杂对氧空位形成和 O/DCM 吸附的积极影响。DCM 催化臭氧化的可能机制包括 O/DCM 吸附、O 活化、DCM 氧化和电子补充四个部分。本文为温和条件下催化消除氯代烷烃提供了新的思路。