Biohydrogenated Diesel from Palm Oil Deoxygenation over Unsupported and γ-Al2O3 Supported Ni-Mo Catalysts

被引:13
|
作者
Aiamsiri, Pojawan [1 ,2 ]
Tumnantong, Dusadee [1 ]
Yoosuk, Boonyawan [3 ]
Ngamcharussrivichai, Chawalit [4 ,5 ]
Prasassarakich, Pattarapan [1 ,2 ]
机构
[1] Chulalongkorn Univ, Fac Sci, Dept Chem Technol, Bangkok 10330, Thailand
[2] Chulalongkorn Univ, Ctr Excellence Petrochem & Mat Technol PETROMAT, Bangkok 10330, Thailand
[3] Natl Sci & Technol Dev Agcy NSTDA, Clean Fuel Technol & Adv Chem Res Team, Natl Energy Technol Ctr ENTEC, Khlong Luang 12120, Pathum Thani, Thailand
[4] Chulalongkorn Univ, Fac Sci, Dept Chem Technol, Ctr Excellence Petrochem & Mat Technol PETROMAT, Bangkok 10330, Thailand
[5] Chulalongkorn Univ, Ctr Excellence Catalysis Bioenergy & Renewable Ch, Fac Sci, Bangkok 10330, Thailand
关键词
MODEL-COMPOUND; OLEIC-ACID; HEAVY OIL; HYDRODEOXYGENATION; FUEL; HYDROCARBONS; PHENOL; HYDRODESULFURIZATION; KINETICS; BIOFUEL;
D O I
10.1021/acs.energyfuels.1c02083
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
This research work aimed to investigate the performance of unsupported and gamma-Al2O3 supported nickel- molybdenum (Ni-Mo) catalysts for palm oil deoxygenation to biohydrogenated diesel. Three preparation methods of supported catalyst (one-step hydrothermal, physical mixing, and incipient wetness impregnation) were studied. In all experiments, the main products were n-alkanes (n-C-14, n-C-15, n-C-16, n-C-17, and n-C-18). For palm oil deoxygenation over an unsupported NiMoS2 catalyst, increasing the palm oil concentration enhanced the decarbonylation (DCO) and decarboxylation (DCO2) pathways, while prolonging the reaction time led to an increased relative rate of hydrodeoxygenation (HDO) rather than DCO and DCO2 reactions. The unsupported 0.2-NiMoS2 catalyst (at a Ni/[Ni + Mo] molar ratio of 2) prepared by a hydrothermal method was the efficient catalyst, while the appropriate reaction conditions were 300 degrees C for 3 h at an initial hydrogen pressure of 40 bar, with a catalyst/palm oil ratio of 0.1, to give the highest C14-18 alkane yield of 67.0 wt %. The selectivities for n-C-15, n-C-16, n-C-17, and n-C-18 alkanes were 19.6%, 20.2%, 26.8%, and 33.0%, respectively. A new supported NiMoS2 catalyst prepared by a one-step hydrothermal method was proposed. This technique merges the advantages of both an alumina (Al2O3) support and our previous hydrothermal method. The H-NiMoS2/gamma-Al2O3 supported catalyst with a 20 wt % Al2O3 loading (H-NiMoS2/gamma-Al2O3 -0.2) prepared by the hydrothermal method presented a higher dispersion of Ni-Mo-S species than the unsupported catalyst, which results from the Al2O3 support. Without needing further presulfidation, the H-NiMoS2/gamma-Al2O3-0.2 catalyst showed good HDO activity under appropriate conditions, which gave a high C14-18 yield of 55.4 wt % and a selectivities for n-C-15, n-C-16, n-C-17, and n-C-18 of 14.1%, 25.3%, 19.7%, and 36.3%, respectively. The 0.2-NiMoS 2 and H-NiMoS2/gamma-Al2O3-0.2 catalysts could be reused for at least three cycles of deoxygenation while maintaining a good performance.
引用
收藏
页码:14793 / 14804
页数:12
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