Synthesis of C4 olefins from n-butane over a novel VOx/SnO2-ZrO2 catalyst using CO2 as soft oxidant

被引:50
作者
Raju, Gangadhara [1 ,2 ]
Reddy, Benjaram M. [2 ]
Abhishek, Burri [1 ]
Mo, Yong-Hwan [1 ]
Park, Sang-Eon [1 ]
机构
[1] Inha Univ, Lab Nanogreen Catalysis, Dept Chem, Inchon 402751, South Korea
[2] Indian Inst Chem Technol, Inorgan & Phys Chem Div, Hyderabad 500607, Andhra Pradesh, India
关键词
n-Butane; 1,3-Butadiene; Soft oxidant; CO2; VOx/SnO2-ZrO2; OXIDATIVE DEHYDROGENATION; CARBON-DIOXIDE; SUPPORTED CATALYSTS; SURFACE-STRUCTURES; ETHYLBENZENE; STYRENE; PERFORMANCE; REACTIVITY; ALKANES; BULK;
D O I
10.1016/j.apcata.2012.02.040
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 (ODH) of n-butane was investigated over ZrO2, SnO2 and SnO2-ZrO2 mixed oxide supported vanadium oxide catalysts with the aim of utilizing CO2 as the soft oxidant, and to study the effect of mixed oxide support on the ODH activity and C4 olefins selectivity. The acid-base properties, reducibility, surface area and morphology of the SnO2-ZrO2 mixed oxide and its individual component oxide supported vanadium oxide samples were thoroughly studied. The mixed oxide supported vanadia sample exhibited superior acid-base bifunctionality: in particular, more numbers of medium strength acid-base sites were observed. The reduction temperature of the vanadia was observed to decrease in the case of mixed oxide supported vanadia catalysts. The mixed oxide supported vanadia sample exhibited a high conversion and product selectivity than its individual component oxide supported vanadia samples. A significant difference in the catalyst activity was noted in the presence and absence (He) of CO2 feed gas. Among various catalysts evaluated. the VOx/SnO2-ZrO2 catalyst exhibited excellent performance (22.34 and 36.63% conversion of n-butane and selectivity of C4 olefins, respectively), which is attributed to a high specific surface area, superior acid-base bifunctionality and easily reducibility of the dispersed vanadium oxide. (C) 2012 Elsevier B.V. All rights reserved.
引用
收藏
页码:168 / 175
页数:8
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