A novel manganese tungstate nanorod catalyst for the oxidation of styrene with tert-butyl hydroperoxide as oxidant

被引:0
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作者
Shanmugam Manimaran [1 ]
Arumugam Pandurangan [1 ]
Gopalakrishnan Govindasamy [2 ]
机构
[1] Department of Chemistry , Anna University
[2] Energy Cluster, School of Engineering , University of Petroleum and Energy Studies
关键词
D O I
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中图分类号
TQ426 [催化剂(触媒)]; TB383.1 [];
学科分类号
080502 ; 081705 ;
摘要
Catalyst,solvent and process parameters are the keys for the selective oxidation of styrene and other olefins to value added intermediates.Hence MnWO4 was synthesized by the one-pot hydrothermal method using Pluronic F127 as a surfactant,characterized and evaluated for the oxidation of styrene and different olefins,using tert-butyl hydroperoxide(TBHP) as oxidant.X-ray diffractogram confirmed the phase purity of MnWO4 which became further evident from the near surface equimolar proposition of Mn and W in+2 and+6 oxidation states,respectively,as inferred from X-ray photoelectron spectra.N2 sorption followed type Ⅳa isotherm with H3 hysteresis loop,starting at the relative pressure(P/P_o) of 0.9,typically of mesoporous materials containing macropores as further confirmed by pore-size distribution.Transmission electron microscope images of MnWO4 revealed its nanorod morphology.In the absence of catalyst,styrene conversion was 35%with benzaldehyde as the sole product and addition of 75 g of MnWO4 increased the styrene conversion to 97.3%,and the styrene oxide selectivity from 0% to 85% demonstrated its activity and selectivity.For the maximum conversion and styrene oxide selectivity optimum temperature,styrene:TBHP molar ratio,catalyst amount and solvent were found to be 70 ℃,1:2,75 mg,and acetonitrile,respectively.MnWO4 catalyst retained its activity and selectivity for five recycles,confirming its recoverability and reusability.From the kinetic studies,pre-exponential factor and apparent activation energy were found to be 0.206 s-1 and 31.5 kJ·mol-1,respectively,and a reaction mechanism was proposed.MnWO4 catalyst was active for oxidation of alkenes,cycloolefins and alkenyl aromatics with high selectivity for epoxides.
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页码:845 / 858
页数:14
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