Low-temperature hydrodeoxygenation of phenol using modified TiO2(B) nanosheets supported highly dispersed Pt catalyst

被引:8
作者
Li, Xu [1 ,3 ]
Yan, Long [3 ]
Liu, Ziyue [1 ,3 ]
Liao, Yuhe [3 ]
Ma, Longlong [2 ]
机构
[1] Univ Sci & Technol China, Dept Thermal Sci & Energy Engn, Hefei, Peoples R China
[2] Southeast Univ, Sch Energy & Environm, Key Lab Energy Thermal Convers & Proc Measurement, Minist Educ, Nanjing 210096, Jiangsu, Peoples R China
[3] Chinese Acad Sci, Guangzhou Inst Energy Convers, CAS Key Lab Renewable Energy, Guangzhou 510640, Peoples R China
关键词
Phenol; Mild conditions; Hydrodeoxygenation; Modified TiO 2 (B) nanosheets; Highly dispersed Pt; BIO-OIL; LIGNIN; NANOPARTICLES; CONVERSION; ARENES; ROUTE; PHASE;
D O I
10.1016/j.fuel.2022.127314
中图分类号
TE [石油、天然气工业]; TK [能源与动力工程];
学科分类号
0807 ; 0820 ;
摘要
Catalytic hydrodeoxygenation (HDO) of oxygenated compounds is essential for chemical refining, which is al-ways carried out under high temperature, hydrogen pressure or/and strong acids. Herein, we developed a novel Pt/TiO2(B) catalyst for the ambient HDO process. With the modified organic functional TiO2(B) nanosheets, the catalytic activity of Pt/TiO2(B) was significantly improved. Through the synergistic effect of highly dispersed Pt species and TiO2(B) supports, phenol was efficiently converted into cyclohexane and concomitant cyclohexanol under 50 degrees C and atmospheric hydrogen without extra acid. The characterizations of catalysts showed that the introduction of organic functional groups not only led to the formation of highly dispersed Pt species, but was also conducive to the yielding of key HDO intermediates. Due to the low C-O bond energy of enol intermediates, the HDO of phenol could be carried out at mild conditions through the implementable C-O bond cleavage of enol intermediates. This study provides a new understanding of the green HDO process and a novel approach for HDO catalyst development.
引用
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页数:10
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