Hydrodeoxygenation of non-edible bio-lipids to renewable hydrocarbons over mesoporous SiO2-TiO2 supported NiMo bimetallic catalyst

被引:29
作者
Fu, Lin [1 ]
Ba, Wenxia [1 ]
Li, Yongfei [1 ,2 ,3 ]
Li, Xin [1 ]
Zhao, Jingxuan [1 ]
Zhang, Simiao [1 ]
Liu, Yuejin [1 ,2 ,3 ]
机构
[1] Xiangtan Univ, Coll Chem Engn, Xiangtan 411105, Hunan, Peoples R China
[2] Xiangtan Univ, Natl & Local United Engn Res Ctr Chem Proc Simula, Xiangtan 411105, Peoples R China
[3] Xiangtan Univ, Hunan Key Lab Environm Friendly Chem Proc Integra, Xiangtan 411105, Peoples R China
基金
中国国家自然科学基金;
关键词
Bio-lipids; Hydrodeoxygenation; Ni-Mo/SiO2-TiO2; catalysts; eta(2)(CO)-aldehyde configuration; Bronsted acidic sites; WASTE COOKING OIL; STEARIC-ACID; FATTY-ACIDS; GREEN DIESEL; OLEIC-ACID; METHYL-ESTERS; PALMITIC ACID; N-HEPTADECANE; DEOXYGENATION; MO;
D O I
10.1016/j.apcata.2021.118475
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
Ni-catalysts are promising candidate for fatty acid hydrodeoxygenation (HDO), but are limited by their quite poor HDO selectivity. Herein, a mesoporous Ni-Mo/SiO2-TiO2 catalyst was prepared by precipitation and impregnation method and used for methyl laurate HDO, yielding 96.3% n-dodecane yield at full methyl laurate conversion. Non-edible bio-lipids such as jatropha oil and waste cooking oil also converted to n-C14+16+18 hy-drocarbons with yields of 94.3% and 92.4%, respectively. Besides, Ni-Mo/SiO2TiO2 shows strong chemo-selectivity towards the HDO of ester groups. Experimental results showed that Mo-addition and Ti/Si molar ratio strongly influenced HDO selectivity. Oxygen vacancies formed on partial reduced TiO2 surface securely bond Ni NPs and activate C=O/C-O bonds, improving Ni NPs dispersion and promoting R-COOCH3 R-CHO reduction. Additional, Mo-addition switches reactant adsorption configuration from eta(1)(C)-acyl to eta(2)(C,O)-aldehyde, pro-moting the formation of R-CH2OH intermediate. Moreover, abundant Bronsted acidic sites (Mo4+-OH, Mo6+-OH, hydroxy groups) facilitate the HDO of R-CH2OH to R-CH3.
引用
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页数:12
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