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用于烯烃环氧化反应的二氧化钛负载氧化钴——表征、催化活性及机理——采用密度泛函理论模型

TiO supported cobalt oxide for olefin epoxidation reaction - characterization, catalytic activities and mechanism - using a DFT model.

作者信息

Mishra Subhashree, Sangma Simon Watre, Poddar Mukesh Kumar, Bal Rajaram, Singh G P, Dey Ratan Kumar

机构信息

Department of Chemistry, Central University of Jharkhand (CUJ), Ranchi - 835 205, India.

Light and Stock Processing Division, CSIR-Indian Institute of Petroleum (IIP), Dehradun-248005, India.

出版信息

Dalton Trans. 2022 Jul 12;51(27):10486-10500. doi: 10.1039/d2dt01118b.

DOI:10.1039/d2dt01118b
PMID:35766149
Abstract

Metal oxide catalysts are known to trigger C-H bond activation selectively, indicating their suitability for olefin epoxidation. Nano-structured CoO supported on TiO was prepared for selective epoxidation of a number of olefins under optimized reaction conditions. An appropriate synthetic procedure yielded a catalytic material (Co-Ti (NP)) with desired crystal size and interface conditions. Incorporation of Co into the Ti matrix resulted in an enhancement in the specific surface of Ti-Co nanoparticles (77.93 m g). XPS measurements evaluated the surface cobalt atom concentration (5.77%) in Ti-Co(NP), indicating more dispersion of cobalt oxide species. Catalytic application of the material, using various olefins (under optimized reaction conditions) shows higher conversion (>85%) in a 6-h time interval. The substrate : oxidant (HO) concentration in an optimized molar ratio of 1 : 2 shows high olefin conversion for the formation of olefin oxide. The reactivity of olefins was found to be in the order: cyclohexene > methylstyrene > styrene > chlorostyrene > -nitrostyrene. A DFT model compared the HOMO-LUMO energies of styrene and its substituted forms. The reusability of Ti-Co (NP) tested up to four continuous cycles of batch operations indicates a negligible loss (0.25-0.30%) of catalytic activity.

摘要

已知金属氧化物催化剂可选择性地引发C-H键活化,这表明它们适用于烯烃环氧化反应。制备了负载在TiO上的纳米结构CoO,用于在优化的反应条件下对多种烯烃进行选择性环氧化。适当的合成程序产生了具有所需晶体尺寸和界面条件的催化材料(Co-Ti (NP))。将Co掺入Ti基体中导致Ti-Co纳米颗粒的比表面积增加(77.93 m²/g)。XPS测量评估了Ti-Co(NP)中表面钴原子浓度(5.77%),表明氧化钴物种的分散性更高。使用各种烯烃(在优化反应条件下)对该材料进行催化应用,在6小时的时间间隔内显示出更高的转化率(>85%)。底物与氧化剂(H₂O₂)的浓度在优化的摩尔比1:2下,对于形成环氧烯烃显示出高烯烃转化率。发现烯烃的反应活性顺序为:环己烯>甲基苯乙烯>苯乙烯>氯苯乙烯>对硝基苯乙烯。一个DFT模型比较了苯乙烯及其取代形式的HOMO-LUMO能量。对Ti-Co (NP)进行了多达四个连续批次操作循环的可重复使用性测试,结果表明催化活性损失可忽略不计(0.25 - 0.30%)。

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