Waste clamshell-derived CaO supported Co and W catalysts for renewable fuels production via cracking-deoxygenation of triolein

被引:57
|
作者
Asikin-Mijan, N. [1 ,3 ]
Lee, H. V. [1 ]
Juan, J. C. [1 ]
Noorsaadah, A. R. [2 ]
Abdulkareem-Alsultan, G. [3 ]
Arumugam, M. [3 ]
Taufiq-Yap, Y. H. [3 ]
机构
[1] Univ Malaya, Inst Postgrad Studies, Nanotechnol & Catalysis Res Ctr NanoCat, Kuala Lumpur 50603, Malaysia
[2] Univ Malaya, Dept Chem, Fac Sci, Kuala Lumpur 50603, Malaysia
[3] Univ Putra Malaysia, Catalysis Sci & Technol Res Ctr PutraCat, Fac Sci, Upm Serdang 43400, Selangor, Malaysia
关键词
Deoxygenation; Pyrolysis; CaO; Transition metal; Gasoline; Acid-base catalyst; FATTY-ACIDS; BIO-OIL; BIOFUEL PRODUCTION; CARBOXYLIC-ACIDS; OXIDE CATALYSTS; METAL-CATALYSTS; MICROALGAL OIL; VEGETABLE-OILS; PYROLYSIS OIL; HYDROCARBONS;
D O I
10.1016/j.jaap.2016.04.015
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
Cracking-Deoxygenation process is one of the important reaction pathways to produce renewable diesel with desired range of C-8-C-17 from oxygenated biomass liquid via removal of oxygen molecule. Utilization of Ca-based catalyst has attracted much attention in deoxygenation reaction due to its superior physicochemical properties. These type of catalysts capable to remove oxygen from carboxyl group of fatty acid or oil in the form of CO2 and CO via decarboxylation or decarbonylation reaction, respectively. In this study, triolein was used as a model compound for the production of renewable fuels. Furthermore, waste clamshell-derived CaO-based catalysts (Co-CaO and W-CaO) were used as catalysts for the deoxygenation reaction. The liquid product over Co-CaO and W-CaO yielded 32% and 22% of C-8-C-17 hydrocarbon fractions with gasoline selectivity of 75% and 65%, respectively. Co-CaO catalyst with positive effect on cracking-deoxygenation process was further investigated by study the effect of Co content from 10 to 40 wt.%. Results showed that paraffinic hydrocarbon yield was increased from 25% to 65%, while gasoline selectivity increased from 56% to 84% at reaction conditions; 350 degrees C reaction temperature, 45 min reaction time, 5 wt.% catalyst loading, 10 mbar pressure under 40 wt.% of active Co metal. (C) 2016 Elsevier B.V. All rights reserved.
引用
收藏
页码:110 / 120
页数:11
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