不同金属改性剂对Rh/FePO4催化剂氢甲酰化性能的影响

高照华, 宋华兴, 颜晓瑞, 魏海生, 王文华, 任万忠

现代化工 ›› 2022, Vol. 42 ›› Issue (2) : 136 -141.

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现代化工 ›› 2022, Vol. 42 ›› Issue (2) : 136-141. DOI: 10.16606/j.cnki.issn0253-4320.2022.02.028
科研与开发

不同金属改性剂对Rh/FePO4催化剂氢甲酰化性能的影响

    高照华, 宋华兴, 颜晓瑞, 魏海生, 王文华, 任万忠
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Effect of different metal modifiers on performance of Rh/FePO4 catalyst for hydroformylation

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摘要

采用等体积浸渍法制备了不同金属(La、Co、Ce、Cr)改性的M-Rh/FePO4催化剂,考察不同催化剂在1-辛烯氢甲酰化中的反应性能;利用XRD、H2-TPR、XPS等对催化剂进行表征。结果表明,不同改性剂对Rh/FePO4催化剂中金属Rh与载体FePO4改性效果不同,其中金属Cr的加入对Rh/FePO4催化性能的提高明显优于其他3种改性剂,同时,过多金属Cr的加入降低了催化性能。当金属Cr质量分数为0.1%时,可显著增强金属Rh与载体FePO4之间的相互作用,在1-辛烯氢甲酰化反应中表现出较好的催化性能,可获得99.4%的转化率和92.8%的醛收率。催化剂经5次循环反应后仍保持较好的活性和选择性,具有良好的循环稳定性。

Abstract

M-Rh/FePO4 catalysts modified by different metals, such as La, Co, Ce, Cr, are synthesized via incipient impregnation, and characterized by means of XRD, H2-TPR and XPS.Their reaction performances are investigated in the hydroformylation of 1-octene.The results show that different metal modifiers lead to different influences on the interaction between metal Rh and FePO4 support.Among them, Cr demonstrates better catalytic performance than other modifiers.Meanwhile, it is found there exists a suitable adding amount for Cr.Overhigh adding amount will decline the catalytic performance of catalysts, which weakens the interaction between Rh and FePO4.As the adding amount of Cr is 0.1%, it can significantly enhance the interaction between Rh and FePO4.The catalyst with 0.1% of Cr can exhibit good catalytic performance in hydroformylation of 1-octene, over which the conversion of 1-octene can reach 99.4% and the yield can reach 92.8%.The catalyst exhibits excellent activity and stability, which can maintain an unchanged activity and selectivity after five cycles of experiments.

关键词

氢甲酰化 / 催化剂 / 改性 / Rh / 1-辛烯

Key words

hydroformylation / catalyst / modification / Rh / 1-octene

Author summay

高照华(1996-),男,硕士研究生,研究方向为工业催化,zhaohuagao@s.ytu.edu.cn

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不同金属改性剂对Rh/FePO4催化剂氢甲酰化性能的影响[J]. 现代化工, 2022, 42(2): 136-141 DOI:10.16606/j.cnki.issn0253-4320.2022.02.028

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