Tuning the Reaction Selectivity over MgAl Spinel-Supported Pt Catalyst in Furfuryl Alcohol Conversion to Pentanediols

选择性 糠醇 催化作用 尖晶石 化学 纳米颗粒 化学工程 材料科学 纳米技术 有机化学 冶金 工程类
作者
Xinsheng Li,Jifeng Pang,Jingcai Zhang,Xianquan Li,Yu Jiang,Yang Su,Weizhen Li,Mingyuan Zheng
出处
期刊:Catalysts [Multidisciplinary Digital Publishing Institute]
卷期号:11 (4): 415-415
标识
DOI:10.3390/catal11040415
摘要

Catalytic conversion of biomass-derived feedstock to high-value chemicals is of remarkable significance for alleviating dependence on fossil energy resources. MgAl spinel-supported Pt catalysts were prepared and used in furfuryl alcohol conversion. The approaches to tune the reaction selectivity toward pentanediols (PeDs) were investigated and the catalytic performance was correlated to the catalysts’ physicochemical properties based on comprehensive characterizations. It was found that 1–8 wt% Pt was highly dispersed on the MgAl2O4 support as nanoparticles with small sizes of 1–3 nm. The reaction selectivity did not show dependence on the size of Pt nanoparticles. Introducing LiOH onto the support effectively steered the reaction products toward the PeDs at the expense of tetrahydrofurfuryl alcohol (THFA) selectivity. Meanwhile, the major product in PeDs was shifted from 1,5-PeD to 1,2-PeD. The reasons for the PeDs selectivity enhancement were attributed to the generation of a large number of medium-strong base sites on the Li-modified Pt catalyst. The reaction temperature is another effective factor to tune the reaction selectivity. At 230 °C, PeDs selectivity was enhanced to 77.4% with a 1,2-PeD to 1,5-PeD ratio of 3.7 over 4Pt/10Li/MgAl2O4. The Pt/Li/MgAl2O4 catalyst was robust to be reused five times without deactivation.

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