框架锡促进的水热稳定沸石包封金属催化剂

IF 13.1 1区 化学 Q1 CHEMISTRY, PHYSICAL
Xiaoyu Li, Lichen Liu
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引用次数: 0

摘要

水热稳定性是设计实际应用的非均相金属催化剂时考虑的重要性能标准,因为在反应进料或产物中普遍存在水分。在这项工作中,我们通过将锡加入沸石骨架中,大大提高了pt -沸石催化剂的水热稳定性。在850℃的CO + O2 + H2O混合气氛中,水热处理后的MFI沸石结构仍保持良好。在Pt-MFI中加入Sn不仅可以修复纯硅MFI沸石的缺陷部位,提高其水热处理时的结构稳定性,而且还可以通过Sn - o - pt相互作用稳定PtOx。在CO氧化反应中,包裹在sn促进MFI沸石中的Pt颗粒具有非常高的稳定性,在sn促进MFI沸石中稳定的Pt颗粒比未促进的Pt-MFI催化剂表现出更高的稳定性。Sn的稳定作用进一步扩展到Pd- mfi分子筛催化剂上,在850℃的苛刻水热处理下,Pd颗粒的平均尺寸保持在2 nm以下。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Hydrothermally Stable Zeolite-Encapsulated Metal Catalyst Promoted by Framework Sn Species

Hydrothermally Stable Zeolite-Encapsulated Metal Catalyst Promoted by Framework Sn Species
Hydrothermal stability is a vital performance criterion considered in the design of heterogeneous metal catalysts for practical applications because of the widespread presence of moisture in the reaction feeds or the products. In this work, we substantially promote the hydrothermal stability of the Pt-zeolite catalyst by incorporating Sn into the zeolite framework. Pt species are stabilized as small nanoparticles, and the MFI zeolite structure is well preserved even after hydrothermal treatment at 850 °C in a mixed atmosphere (CO + O2 + H2O). Adding Sn into Pt-MFI not only heals the defect sites in pure-silica MFI zeolite to promote its structural stability during hydrothermal treatment but also stabilizes the mobile PtOx species via the Sn–O–Pt interaction. The remarkably high stability of the Pt particles encapsulated in the Sn-promoted MFI zeolite is reflected in the CO oxidation reaction in which Pt particles stabilized in the Sn-promoted MFI zeolite exhibit much higher stability than the nonpromoted Pt-MFI catalyst. The stabilization effect of Sn is further extended to a Pd-MFI zeolite catalyst in which the average size of the Pd particles remains below 2 nm after the harsh hydrothermal treatments at 850 °C.
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来源期刊
ACS Catalysis
ACS Catalysis CHEMISTRY, PHYSICAL-
CiteScore
20.80
自引率
6.20%
发文量
1253
审稿时长
1.5 months
期刊介绍: ACS Catalysis is an esteemed journal that publishes original research in the fields of heterogeneous catalysis, molecular catalysis, and biocatalysis. It offers broad coverage across diverse areas such as life sciences, organometallics and synthesis, photochemistry and electrochemistry, drug discovery and synthesis, materials science, environmental protection, polymer discovery and synthesis, and energy and fuels. The scope of the journal is to showcase innovative work in various aspects of catalysis. This includes new reactions and novel synthetic approaches utilizing known catalysts, the discovery or modification of new catalysts, elucidation of catalytic mechanisms through cutting-edge investigations, practical enhancements of existing processes, as well as conceptual advances in the field. Contributions to ACS Catalysis can encompass both experimental and theoretical research focused on catalytic molecules, macromolecules, and materials that exhibit catalytic turnover.
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