镍改性 MIL-100(Fe)催化剂在 C3H6-SCR 中的反应活性及反应机理

IF 3.4 3区 化学 Q2 CHEMISTRY, PHYSICAL Catalysis Communications Pub Date : 2024-02-01 DOI:10.1016/j.catcom.2024.106854
Shuying Ning , Muhammad Kashif , Wenyi Deng , Bingtao Zhao , Yaxin Su
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引用次数: 0

摘要

采用水热法合成了基于金属有机框架(MOFs)的载体 MIL-100(Fe),并通过湿法浸渍法将 Ni 支持在 MIL-100(Fe) 上,制备了用于 C3H6 选择性催化还原 NO(C3H6-SCR)的催化剂。镍的加入大大提高了 C3H6-SCR 的反应活性。275 °C 时,MIL-100(Fe) 的 NO 转化率为 74.5%,而 5.8%Ni/MIL-100(Fe) 的 NO 转化率为 100%,N2 选择性为 100%。原位 DRIFTS 证明,NO2-/NO3- 与 CxHyOz 物质之间的相互作用产生了中间异氰酸酯(R-NCO),并根据 DRIFTS 结果提出了反应途径,以了解其机理。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Reactivity of Ni-modified MIL-100(Fe) catalysts for C3H6-SCR and reaction mechanism

Metal-organic frameworks (MOFs)-based carrier, MIL-100(Fe), was synthesized by hydrothermal method and Ni was supported on the MIL-100(Fe) by wet impregnation method to prepare the catalysts for selective catalytic reduction of NO with C3H6 (C3H6-SCR). The addition of Ni significantly improved the reactivity of C3H6-SCR. At 275 °C, the NO conversion of MIL-100(Fe) was 74.5%, whereas the NO conversion of 5.8%Ni/MIL-100(Fe) with 100% N2 selectivity was 100%. The in-situ DRIFTS prove that the interaction between NO2/NO3 and CxHyOz substances generated intermediate isocyanates (R-NCO), and the reaction pathway was proposed based on the DRIFTS results to understand the mechanism.

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来源期刊
Catalysis Communications
Catalysis Communications 化学-物理化学
CiteScore
6.20
自引率
2.70%
发文量
183
审稿时长
46 days
期刊介绍: Catalysis Communications aims to provide rapid publication of significant, novel, and timely research results homogeneous, heterogeneous, and enzymatic catalysis.
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