Investigation on the xylitol aqueous-phase reforming performance for pentane production over Pt/HZSM-5 and Ni/HZSM-5 catalysts

被引:55
作者
Jiang, Ting [1 ,2 ]
Wang, Tiejun [1 ]
Ma, Longlong [1 ]
Li, Yuping [1 ]
Zhang, Qing [1 ]
Zhang, Xinghua [1 ]
机构
[1] Chinese Acad Sci, Key Lab Renewable Energy & Gas Hydrate, Guangzhou Inst Energy, Guangzhou, Guangdong, Peoples R China
[2] Chinese Acad Sci, Grad Sch, Beijing, Peoples R China
基金
中国国家自然科学基金;
关键词
Aqueous-phase reforming; Alkane production; Xylitol; Ni/HZSM-5; Pt/HZSM-5; MODIFIED NI CATALYSTS; OXYGENATED HYDROCARBONS; LIQUID ALKANES; HYDROGEN GENERATION; ETHYLENE-GLYCOL; BIOMASS; FUELS; GLYCEROL; SORBITOL; PLATFORM;
D O I
10.1016/j.apenergy.2011.03.034
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
Pt/HZSM-5 and Ni/HZSM-5 catalysts were prepared and evaluated for aqueous-phase reforming (APR) reaction of xylitol. Effects of reaction temperature, pressure and metal loading on xylitol conversion and pentane selectivity were studied. Experiments over 4 wt% Pt/HZSM-5 catalysts showed that high temperature increased the xylitol conversion while high pressure led to the decrease of pentane selectivity. The xylitol conversion and pentane selectivity increased with the metal loading in the range of 0-3 wt%, but the values decreased as further increasing the metal loading to 5 wt% over both Ni/HZSM-5 and Pt/HZSM-5, indicating that higher metal loading would increase the rate of C-C bond cleavage compared to hydrogenation. Under the condition of 240 degrees C and 4 MPa, Ni/HZSM-5 and Pt/HZSM-5 with the same metal loading of 2 wt% showed similar xylitol conversion, while the primary had higher pentane selectivity of 95% than 58% of the latter. Ni has higher activity for pentane production than Pt during the APR reaction of xylitol, while Pt has stronger effect of C-C bond cleavage to produce lighter alkanes of C-1-C-4. In order to investigate catalyst recyclability, 2 wt% Ni/HZSM-5 was reused and analyzed by TG characterization. It was found that considerable amount of coke and heavy hydrocarbons were formed on the catalyst surface, which could cover the active sites and cause catalyst deactivation. (C) 2011 Elsevier Ltd. All rights reserved.
引用
收藏
页码:51 / 57
页数:7
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