An in-situ combo Mo-based ionic liquid and SAPO-11 catalyst for efficient biolipids hydrodeoxygenation and isomerization

被引:5
作者
Ding, Yongxin [1 ]
Lin, Jun [1 ]
Yu, Panjie [1 ]
Zhang, Hongwei [1 ]
Ma, Yongde [1 ]
Cai, Zhenping [1 ]
Cao, Yanning [1 ,2 ]
Huang, Kuan [1 ,2 ]
Jiang, Lilong [1 ,2 ]
机构
[1] Fuzhou Univ, Coll Chem Engn, Natl Engn Res Ctr Chem Fertilizer Catalyst NERC CF, Fuzhou 350002, Fujian, Peoples R China
[2] Qingyuan Innovat Lab, Quanzhou 362801, Fujian, Peoples R China
基金
中国国家自然科学基金;
关键词
Hydrodeoxygenation; Isomerization; Biodiesel; Methyl palmitate; MoS2; SAPO-11; JATROPHA OIL; N-OCTANE; HYDRODESULFURIZATION; LIGNIN;
D O I
10.1016/j.fuel.2023.130827
中图分类号
TE [石油、天然气工业]; TK [能源与动力工程];
学科分类号
0807 ; 0820 ;
摘要
The design of novel practical catalysts is critical for the blossoming of biodiesel green-energy, in which Mo-based catalysts are of particular interest. In this work, an in-situ synthesis method was proposed to obtain a combo Mo-based ionic liquid and SAPO-11 catalyst. The catalyst presents both highly dispersed MoS2 as hydrodeoxygenation active sites and acidic sites for isomerization. MoS2 with a few fine layers can be identified based on TEM images and the Bronsted acid sites are dominant based on Pyridine-IR analysis. A great performance of MoS2/C(8)min-15 %SA can be obtained under optimized reaction conditions with 100 % conversion of methyl palmitate, 75.0 mol% hydrodeoxygenation to n-C-15-C-16, and 20.5 mol % isomerization to i-C-15-C-16. The structure and activity of the catalyst can be retained at least for 4 cycles. Thin layers and high sulfurization, large amount of Br & oslash;nsted acid sites, and suitable reaction conditions are key points to achieve a significant performance and avoid over cracking and deactivation. On basis of detected intermediates and kinetic data simulations, a complex reaction pathway was proposed and the specific k values for each elementary reaction were provided for the hydrodeoxygenation and isomerization of methyl palmitate.
引用
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页数:11
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