Ethylbenzene to styrene over alkali doped TiO2-ZrO2 with CO2 as soft oxidant

被引:33
作者
Burri, Abhishek [1 ]
Jiang, Nanzhe [1 ,2 ]
Yahyaoui, Khalid [3 ]
Park, Sang-Eon [1 ]
机构
[1] Inha Univ, Dept Chem & Chem Engn, Lab Nanogreen Catalysis, Inchon 402751, South Korea
[2] Yanbian Univ, Dept Chem Engn, Yanbian, Peoples R China
[3] Saudi Basic Ind Corp, Riyadh 11422, Saudi Arabia
关键词
Oxidative dehydrogenation; CO2; conversion; Soft oxidant; Mixed metal oxides; Styrene; OXIDATIVE DEHYDROGENATION; CARBON-DIOXIDE; SURFACE-AREA; MIXED OXIDES; NONOXIDATIVE DEHYDROGENATION; CATALYTIC-ACTIVITY; DEACTIVATION; OXIDEHYDROGENATION; PERFORMANCE; ACTIVATION;
D O I
10.1016/j.apcata.2015.02.003
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
Oxidative dehydrogenation of ethylbenzene (EB) to styrene monomer (SM) over alkali metal (Na, K) doped TiO2-ZrO2 (TZ) has been studied. The EB and CO2 conversions observed over alkali doped TZ are higher than that of non-doped TZ. The enhanced CO2 conversion compared with non-doped counterparts is attributed to improved basicity, formation of TiZrO4 phase with increased CO2 affinity and insertion of K or Na into the lattice which affects the binding energy of "O" in turn providing more labile oxygen species. Alkali doping also effected in fine tuning the surface acid base properties. Moreover, these K and Na doped binary metal oxides system showed high surface area of 256 m(2)/g and 199 m(2)/g respectively. There was a 10-fold increase in the CO2 conversions in case of the doped TZ compared to non-doped TZ increasing the stability of the catalyst by decreasing coking on the surface of the catalyst in spite of the high conversions. (C) 2015 Elsevier B.V. All rights reserved.
引用
收藏
页码:192 / 199
页数:8
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