介质阻挡放电等离子体对SiO2负载cu基乙炔水化催化剂的影响

IF 4.9 2区 化学 Q2 CHEMISTRY, PHYSICAL Molecular Catalysis Pub Date : 2025-03-29 DOI:10.1016/j.mcat.2025.115064
Yi Cui, Xiejie Chen, Jiaxuan Gao, Shui Liu, Denghao Wang, Caixia Xu
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引用次数: 0

摘要

提高乙炔水化催化剂的催化性能是目前研究的一个巨大挑战。首先以SiO2为载体,通过介质阻挡放电等离子体合成cu基催化剂用于乙炔水化反应,在8 h的反应时间内,乙炔的转化率为95.9%,乙醛的选择性为83.6%。在反应时间30h内,选择性表现出相对稳定的稳定性。x射线光电子能谱(XPS)和x射线衍射(XRD)结果表明,等离子体处理促进了活性组分与载体的相互作用,从而提高了活性组分的抗还原性能。透射电镜(TEM)和乙炔程序升温解吸(C2H2-TPD)结果表明,等离子体处理显著改善了Cu的分散性,提高了乙炔的吸附能力,从而提高了催化性能。
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Effect of the dielectric barrier discharge plasma on Cu-based catalysts supported on SiO2 for acetylene hydration
Enhancing the catalytic performance of acetylene hydration catalysts remains a formidable challenge in current research. SiO2 was firstly employed as a support to synthesize Cu-based catalysts by dielectric barrier discharge plasma for the acetylene hydration reaction, achieving an impressive conversion of 95.9 % for acetylene and selectivity of 83.6 % for acetaldehyde within 8 h reaction time. The selectivity exhibits a relatively consistent stability within 30 h of reaction time. According to X-ray photoelectron spectroscopy (XPS) and X-ray diffraction (XRD), plasma treatment promotes the interaction between the active component and the support, which can enhance the anti-reduction properties of active copper components. Transmission electron microscopy (TEM) and acetylene temperature-programmed desorption (C2H2-TPD) reveal that plasma treatment markedly improves the dispersion of Cu species and enhances the acetylene adsorption capacity, thereby leading to an improvement in catalytic performance.
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来源期刊
Molecular Catalysis
Molecular Catalysis Chemical Engineering-Process Chemistry and Technology
CiteScore
6.90
自引率
10.90%
发文量
700
审稿时长
40 days
期刊介绍: Molecular Catalysis publishes full papers that are original, rigorous, and scholarly contributions examining the molecular and atomic aspects of catalytic activation and reaction mechanisms. The fields covered are: Heterogeneous catalysis including immobilized molecular catalysts Homogeneous catalysis including organocatalysis, organometallic catalysis and biocatalysis Photo- and electrochemistry Theoretical aspects of catalysis analyzed by computational methods
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