催化作用
沸石
介孔材料
化学工程
选择性
吸附
层状双氢氧化物
乙酸乙酯
降级(电信)
硅酸盐
化学
非热等离子体
化学稳定性
无机化学
等离子体
材料科学
有机化学
电信
物理
量子力学
计算机科学
工程类
作者
Xiang Li,Min Xu,Xiaoqiang Zhang,Jinbao Zheng,Jianjun Li,Di Chen,Binghui Chen
出处
期刊:Langmuir
[American Chemical Society]
日期:2025-02-25
标识
DOI:10.1021/acs.langmuir.4c05254
摘要
The ever-increasing emissions of volatile organic compounds (VOCs) from industrial activities pose significant environmental and health risks. Nonthermal plasma (NTP) degradation technology has emerged as a prominent method for VOC degradation due to the mild reaction conditions but demands an efficient catalyst for high product conversion. This study presents a mesoporous layered NiFe double silicate catalyst fabricated by the reaction between 13X zeolite and layered double hydroxides (LDHs). Under NTP conditions, the catalysts achieved a 90% ethyl acetate conversion with a CO2 selectivity of 45%, maintaining stability over 400 min. The performance demonstrates synergy in adsorption and offers more active catalytic sites on the in situ-generated layered NiFe double silicate over zeolite catalyst. Simulation results also suggested that the two-dimensional sheet structure effectively localizes the electric field on the zeolite surface and therefore may facilitate the generation of active species with plasma and ethyl acetate adsorption. This work provides a pathway for the design of highly efficient and stable catalysts for NTP applications.
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