Guaiacol Hydrodeoxygenation and Hydrogenation over BimetallicPt-M (Nb, W, Zr)/KIT-6 Catalysts with Tunable Acidity

被引:21
作者
Xiao, Yang [2 ,3 ]
Ramanathan, Anand [1 ]
Subramaniam, Bala [1 ]
Varma, Arvind [2 ]
机构
[1] Univ Kansas, Ctr Environmentally Beneficial Catalysis, Dept Chem & Petr Engn, Lawrence, KS 66045 USA
[2] Purdue Univ, Davidson Sch Chem Engn, W Lafayette, IN 47907 USA
[3] Louisiana Tech Univ, Inst Micromfg, Ruston, LA 71272 USA
来源
ACS SUSTAINABLE CHEMISTRY & ENGINEERING | 2022年 / 10卷 / 15期
关键词
Full hydrodeoxygenation; Guaiacol; Bimetallic PtNb PtW PtZr catalysts; Mesoporous KIT-6 support; Tunable acidity; Biofuels; Bio-oil; VAPOR-PHASE HYDRODEOXYGENATION; BIO-OIL; MESOPOROUS SILICATE; DEOXYGENATION; SUPPORT; NI; AROMATICS; GLYCEROL; MODEL; CONVERSION;
D O I
10.1021/acssuschemeng.1c07071
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Owing to a high oxygen content, bio-oils from the fastpyrolysis of biomass require upgrading to meet fuel specification standards.Catalytic hydrodeoxygenation (HDO) of bio-oils faces several challenges suchas low hydrocarbon yields, the requirement of high H2partial pressure forcomplete deoxygenation, and catalyst deactivation caused by coking/carbondeposition. In the present work, Pt supported on Nb, W, and Zr-incorporatedKIT-6 materials were prepared, characterized, and tested for the gas-phaseHDO of guaiacol, a widely used model compound of bio-oil. Facile HDO ofguaiacol was observed over a 1 wt % Pt/Nb-KIT-6 catalyst, with similar to 90%conversion and similar to 75% hydrocarbon selectivity under relatively mild hydrogenpartial pressure (0.5 MPa) at 400 degrees C and 33 h-1weight hourly space velocity(WHSV). No significant catalyst deactivation was observed during a 24-hcontinuous run indicating that the mesoporous support provides enhancedcoking resistance. Mechanistic investigations indicate that the tunable acidity of the supports promotes transalkylation reactions,which favor increased aromatic hydrocarbon yields. A plausible reaction mechanism is postulated based on correlating the number ofmetal and acid sites with the measured rates for the individual reaction steps.
引用
收藏
页码:4831 / 4838
页数:8
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