原位合成用于 1-己烯加氢甲酰化的 Rh@NaX 催化剂

IF 6.7 1区 工程技术 Q2 ENERGY & FUELS Fuel Pub Date : 2024-07-04 DOI:10.1016/j.fuel.2024.132327
Gongcheng Sun, Wan Chen, Yaoying Li, Subing Fan, Junmin Lv, Tiansheng Zhao
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引用次数: 0

摘要

加氢甲酰化反应在工业中非常重要。然而,贵金属铑(Rh)的浸出和均相催化剂的分离一直是难以解决的问题。即使开发了异相铑基催化剂来解决分离问题,但铑的严重流失仍然难以避免。本研究采用一步合成法制备了异相封装的 Rh@NaX,并将其作为催化剂用于 1- 己烯加氢甲酰化反应中的无还原反应。Rh@NaX 催化剂具有优异的催化性能。有趣的是,与浸渍催化剂相比,封装催化剂具有更高的回收稳定性和更低的 Rh 浸出率。此外,还进行了原位 XPS 和 DRIFT 分析,以阐明 Rh 的还原过程和反应途径。
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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In situ synthesis of Rh@NaX catalyst for 1-hexene hydroformylation
The hydroformylation reaction is very important in industry. However, the leaching of the noble metal Rhodium (Rh) and the separation of homogeneous catalyst have always been difficult problems to solve. And even heterogeneous Rh-base catalyst was developed to solve the separation problem, the serious Rh losing is still hard to avoid. In this work, heterogeneous encapsulated Rh@NaX was prepared by using one-step synthesis method and used as catalyst without reduction in 1-hexene hydroformylation reaction. Rh@NaX catalyst exhibited outstanding catalytic performance. When directly complexed with ligand triphenylphosphine (PPh), it achieved high heptanal yield of 97.53 %, high n/i ratio of 2.59 and high TOF of 6588 h. Interestingly, encapsulated catalyst exhibited higher recycling stability and much lower Rh leaching compared to impregnated catalyst. In addition, in situ XPS and DRIFT analyses were conducted to elucidate the reduction process of Rh and the reaction pathway.
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来源期刊
Fuel
Fuel 工程技术-工程:化工
CiteScore
12.80
自引率
20.30%
发文量
3506
审稿时长
64 days
期刊介绍: The exploration of energy sources remains a critical matter of study. For the past nine decades, fuel has consistently held the forefront in primary research efforts within the field of energy science. This area of investigation encompasses a wide range of subjects, with a particular emphasis on emerging concerns like environmental factors and pollution.
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