Enhancing Hydrodeoxygenation of Bio-oil via Bimetallic Ni-V Catalysts Modified by Cross-Surface Migrated-Carbon from Biochar

加氢脱氧 生物炭 催化作用 吸附 材料科学 热解 甲苯 碳化 空间速度 选择性 碳纤维 有机化学 无机化学 化学工程 化学 复合数 工程类 复合材料
作者
Yujian Wu,Yan Sun,Kaili Liang,Zhengguang Yang,Ren Tu,Xudong Fan,Shuchao Cheng,Haipeng Yu,Enchen Jiang,Xiwei Xu
出处
期刊:ACS Applied Materials & Interfaces [American Chemical Society]
卷期号:13 (18): 21482-21498 被引量:43
标识
DOI:10.1021/acsami.1c05350
摘要

Aromatics from selective hydrodeoxygenation (HDO) of biomass-derived bio-oil are an ideal feedstock for replacing industrial fossil products. In this study, biochar-modified Hβ/Ni-V catalysts were prepared and tested in the atmospheric HDO of guaiacol and bio-oil to produce aromatics. Compared with unmodified Hβ/Ni-V, higher HDO activity was achieved in catalysts with all kinds of biochar modifications. Especially, the pine nut shell biochar (PB)-modified PB-Hβ-8/Ni-V showed the highest selectivity to aromatics (69.17%), mainly including benzene and toluene. Besides, under the conditions of 380 °C and weight hourly space velocity (WHSV) of 0.5 h–1, the cleavage of CAr–OH (CAr means the carbon in the benzene ring) was promoted to form more aromatics. Moreover, great recyclability (58.77% aromatics for the reactivated run-3 test) and efficient HDO of bio-oil (44.9% aromatic yield) were also achieved. Based on the characterization results, the enhanced aromatic selectivity of PB-Hβ-8/Ni-V was attributed to the synergetic effect between PB and Hβ/Ni-V. In detail, a stable surface migrated-carbon layer was formed on Hβ/Ni-V via the metal catalytic chemical vapor deposition (CVD) process of the pyrolysis PB volatiles. Simultaneously, a carbothermal reduction driven by the migrated-carbon took place to decorate the surface metals, obtaining more Ni0 and V3+ active sites. With this synergism, increased Ni0 sites promoted H2 adsorption and dissociation, which improved the hydrogenation activity. Furthermore, the higher affinity of the reactant and increased oxygen vacancies both contributed to enhancing the selective surface adsorption of oxygenous groups and the cleavage of the CAr–OH bond, thus improving the deoxygenation activity. Therefore, the HDO activity was improved to form more target aromatics over biochar-modified catalysts. This work highlighted a potential avenue to develop economic and environmental catalysts for the upgrading of bio-oil.
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