Kinetic and Thermodynamic Analysis of Guaiacol Hydrodeoxygenation

被引:31
作者
Sulman, Alexandrina [1 ]
Maki-Arvela, Paivi [1 ]
Bomont, Louis [1 ]
Alda-Onggar, Moldir [1 ]
Fedorov, Vyacheslav [1 ]
Russo, Vincenzo [2 ]
Eranen, Kari [1 ]
Peurla, Markus [3 ]
Akhmetzyanova, Uliana [4 ]
Skuhrovcova, Lenka [4 ]
Tisler, Zdenek [4 ]
Grenman, Henrik [1 ]
Warna, Johan [1 ]
Murzin, Dmitry Yu. [1 ]
机构
[1] Abo Akad Univ, Johan Gadolin Proc Chem Ctr, Turku, Finland
[2] Univ Napoli Federico II, Via Cintia 4, IT-80126 Naples, Italy
[3] Univ Turku, Turku, Finland
[4] Unipetrol Ctr Res & Educ UniCRE, Chempk Litvinov,Block 2838,Zaluzi 1, Litvinov 43670, Czech Republic
关键词
Guaiacol; Hydrodeoxygenation; Carbide; Kinetics; Thermodynamics; VAPOR-PHASE HYDRODEOXYGENATION; SINGLE-SOURCE ROUTE; SELECTIVE HYDRODEOXYGENATION; ACTIVATED CARBON; MODEL-COMPOUND; CATALYSTS; LIGNIN; CARBIDE; ANISOLE; NANOFIBER;
D O I
10.1007/s10562-019-02856-x
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
Kinetics of guaiacol hydrodeoxygenation (HDO) was studied using supported MoxC-SBA-15 and as a comparison 5wt% Pt/C under 30bar hydrogen at 200 degrees C and 300 degrees C. Catalyst characterization was done by a range of physical methods including also determination of the amount of coke and the nature of adsorbed species. Pt/C gave 2-methoxycyclohexanol as the main product, whereas Mo2C-SBA-15 promoted direct deoxygenation exhibiting also strong adsorption of guaiacol on the catalyst surface and formation of oligomers. Thermodynamics of guaiacol HDO was elucidated and the reaction network was proposed based on which kinetic modelling was done. [GRAPHICS] .
引用
收藏
页码:2453 / 2467
页数:15
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