Effect of TiO2 in supported NiWS catalysts for the hydrodeoxygenation of guaiacol

被引:14
|
作者
Garcia-Mendoza, C. [1 ]
Santolalla-Vargas, C. E. [2 ]
Woolfolk, Luis G. [1 ]
del Angel, P. [3 ]
de los Reyes, J. A. [1 ]
机构
[1] Univ Autonoma Metropolitana Iztapalapa, Div Ciencias Basicas & Ingn, Av San Rafael Atlixco 186, Ciudad De Mexico 09340, Mexico
[2] Inst Politecn Nacl, Ctr Interdisciplinario Invest & Estudios Medio Am, Dept Biociencias & Ingn, Calle 30 Junio 1520, Ciudad De Mexico 07340, Mexico
[3] Inst Mexicano Petr, Eje Cent Lazaro Cardenas 152, Ciudad De Mexico 07730, Mexico
关键词
Hydrodeoxygenation; Guaiacol; Bifunctional catalyst; NiWS; TiO2; HYDRODESULFURIZATION CATALYSTS; HYDROTREATING CATALYSTS; EPOXIDE REARRANGEMENT; SURFACE-CHEMISTRY; OXIDE; TIO2-ZRO2; ACID; PYROLYSIS; BIOMASS; CONVERSION;
D O I
10.1016/j.cattod.2020.08.026
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
A series of NiWS catalysts supported on TiO2, ZrO2 and TiO2-ZrO2 mixed oxides was tested in the hydrodeoxygenation of guaiacol. The TiO2/ZrO2 ratio in the mixed oxides was varied to elucidate the effect of the titania content on the catalyst activity. According to our results, high acidity values seem to favor the demethylation route with catechol as the main product, while a medium acid strength could probably be the active site for the scission of the Caromatic-OCH3 bond. Moreover, the production of completely deoxygenated compounds was directly related with the TiO2 percentage on the catalysts. In this sense, guaiacol needs to be converted by the demethoxylation route, in order to avoid the catechol formation, which is a coke precursor, and phenol production route is improved. A fair correlation between medium acid strength for the catalysts and the phenol formation was also found. The catalyst supported on TiO2 was found to be the most active per atom of metal, 62% higher than the NiW/TZ(80/20) catalysts. The content of titania on the support was relevant to obtain completely deoxygenated compounds, such as cyclohexane and benzene.
引用
收藏
页码:145 / 156
页数:12
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