Catalytic evaluation of mesoporous metal oxides for liquid phase oxidation of styrene

被引:62
|
作者
Masunga, Ngonidzashe [1 ]
Tito, Ginny Sasha [1 ]
Meijboom, Reinout [1 ]
机构
[1] Univ Johannesburg, Dept Chem, POB 524, ZA-2006 Johannesburg, South Africa
基金
新加坡国家研究基金会;
关键词
Mesoporous metal oxides; Inverse micelle; Hybrid oxide; Oxidation of styrene; Styrene oxide; SELECTIVE OXIDATION; CONTROLLED POROSITY; NANOPARTICLES; EPOXIDATION; BENZALDEHYDE; NANOSTRUCTURES; REDUCTION; CO3O4; TIO2; O-2;
D O I
10.1016/j.apcata.2017.12.010
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Mesoporous manganese oxide, cobalt oxide, and hybrid Mn-Co oxide were synthesized using an inverse surfactant micelle method. The synthesized materials were monodispersed nanoparticle aggregates with connected and well defined infra-particle voids. An increase in the pore and crystallite size with increase in calcination temperature was observed with TEM, SEM, p-XRD, and N-2-sorption. These mesoporous metal oxides were employed in the selective oxidation of styrene using tert-butyl hydrogen peroxide as an oxidant. Higher selectivity towards styrene oxide was achieved using manganese oxide followed by cobalt oxide while the hybrid oxide showed the lowest selectivity towards styrene oxide. The catalytic activities of the compared catalysts were decreasing in the order of Mn-Co_350 (66.6 h(-1)) > MnO2_350 (47.4 h(-1)) > Co3O4_350 (35.6 h(-1)). The catalytic activities and selectivity profiles under various reaction conditions such as solvent type, catalyst amount, styrene to TBHP ratio and temperature are discussed. The catalytic recyclability of metal oxides showed that they are stable, and the structure of the catalyst was retained.
引用
收藏
页码:154 / 167
页数:14
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