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炔烃选择性加氢制烯烃反应的研究进展

吴泽亮 管琦卉 陈世霞 王珺

化工进展2024,Vol.43Issue(8):4366-4381,16.
化工进展2024,Vol.43Issue(8):4366-4381,16.DOI:10.16085/j.issn.1000-6613.2023-1181

炔烃选择性加氢制烯烃反应的研究进展

Advances in selective hydrogenation of alkynes to alkenes

吴泽亮 1管琦卉 2陈世霞 2王珺2

作者信息

  • 1. 南昌大学资源与环境学院,江西 南昌 330031
  • 2. 南昌大学化学化工学院,江西 南昌 330031
  • 折叠

摘要

Abstract

Selective hydrogenation of alkynes to produce alkenes is a crucial reaction process in petroleum and chemical engineering.Traditional thermal catalytic methods have been extensively studied over the past few decades,while the research on emerging photo-/electrocatalytic methods is still in its preliminary stage and designing highly efficient catalysts remains a significant challenge.The rapid progress in catalyst synthesis methods,structural characterization techniques,and theoretical calculations has gradually revealed the reaction mechanisms and the mechanisms of catalytic active sites involved in the selective hydrogenation of alkynes.This review provides an overview of recent advancements in various catalysts for selective hydrogenation of alkynes and summarizes the corresponding strategies for designing high-performance catalysts.A comparison between traditional thermal catalytic hydrogenation and photo-/electrocatalytic selective hydrogenation routes is made,with a focus on the different characteristics and analysis of the problems and their possible solutions in various types of catalytic hydrogenation reactions.Furthermore,a concise overview of the current research status in this field is provided,along with the major challenges and future development trends.Additionally,the review highlights the potential directions in catalyst design and modulation of target product selectivity for future research.

关键词

炔烃选择性加氢/热催化/光催化/电催化

Key words

selective catalytic hydrogenation of alkynes/thermocatalytic/photocatalysis/electrocatalytic

分类

化学化工

引用本文复制引用

吴泽亮,管琦卉,陈世霞,王珺..炔烃选择性加氢制烯烃反应的研究进展[J].化工进展,2024,43(8):4366-4381,16.

基金项目

国家自然科学基金(22322807). (22322807)

化工进展

OA北大核心CSTPCD

1000-6613

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