Chemical conversion of cellulose as treated in supercritical methanol

被引:115
作者
Ishikawa, Y [1 ]
Saka, S [1 ]
机构
[1] Kyoto Univ, Grad Sch Energy Sci, Dept Socioenvironm Energy Sci, Sakyo Ku, Kyoto 6068501, Japan
关键词
cellulose; chemical conversion; decomposition rate constant; methanolysis; supercritical methanol;
D O I
10.1023/A:1013170020469
中图分类号
TB3 [工程材料学]; TS [轻工业、手工业、生活服务业];
学科分类号
0805 ; 080502 ; 0822 ;
摘要
The chemical conversion of cellulose as treated in supercritical methanol was studied using a batch-type reaction vessel at temperatures from 220 to 450 degreesC and pressures from 14 to 72 MPa. Supercritical methanol treatment at 350 degreesC and 43 MPa for 7 min was sufficient to convert microcrystalline cellulose (avicel) to the methanol-soluble. To study the kinetics of the decomposition of cellulose, the decomposition rate constants were obtained, and rapid increase was observed at about 270 degreesC which was about 30 degreesC higher than the critical temperature of methanol. The main products from cellulose decomposition were methylated cellotriose, methylated cellobiose, methyl alpha- and beta -D-glucosides, levoglucosan and 5-hydroxymethylfurfural. Monomeric compounds such as methyl alpha- and beta -D-glucosides were stable in supercritical methanol, allowing high yields of monomeric products by supercritical methanol treatment. Based on these results, a pathway of cellulose decomposition treated in supercritical methanol was proposed. These findings suggest that the supercritical methanol treatment of various cellulosic materials may be suitable to obtain useful chemicals and liquid fuels without using fossil resources.
引用
收藏
页码:189 / 195
页数:7
相关论文
共 16 条
[1]  
Camacho F, 1996, J CHEM TECHNOL BIOT, V67, P350, DOI 10.1002/(SICI)1097-4660(199612)67:4<350::AID-JCTB564>3.0.CO
[2]  
2-9
[3]   QUANTITATIVE X-RAY INVESTIGATIONS ON THE CRYSTALLINITY OF CELLULOSE FIBERS - A BACKGROUND ANALYSIS [J].
HERMANS, PH ;
WEIDINGER, A .
JOURNAL OF APPLIED PHYSICS, 1948, 19 (05) :491-506
[4]   Temperature effect on continuous gasification of microalgal biomass: theoretical yield of methanol production and its energy balance [J].
Hirano, A ;
Hon-Nami, K ;
Kunito, S ;
Hada, M ;
Ogushi, Y .
CATALYSIS TODAY, 1998, 45 (1-4) :399-404
[5]   GLUCOSE HYDROLYSIS AND OXIDATION IN SUPERCRITICAL WATER [J].
HOLGATE, HR ;
MEYER, JC ;
TESTER, JW .
AICHE JOURNAL, 1995, 41 (03) :637-648
[6]   Glucose and fructose decomposition in subcritical and supercritical water: Detailed reaction pathway, mechanisms, and kinetics [J].
Kabyemela, BM ;
Adschiri, T ;
Malaluan, RM ;
Arai, K .
INDUSTRIAL & ENGINEERING CHEMISTRY RESEARCH, 1999, 38 (08) :2888-2895
[7]   Kinetics of transesterification in rapeseed oil to biodiesel fuel as treated in supercritical methanol [J].
Kusdiana, D ;
Saka, S .
FUEL, 2001, 80 (05) :693-698
[8]   SUPERCRITICAL GAS EXTRACTION OF WOOD WITH METHANOL [J].
LABRECQUE, R ;
KALIAGUINE, S ;
GRANDMAISON, JL .
INDUSTRIAL & ENGINEERING CHEMISTRY PRODUCT RESEARCH AND DEVELOPMENT, 1984, 23 (01) :177-182
[9]  
Medve J, 1998, BIOTECHNOL BIOENG, V59, P621, DOI [10.1002/(SICI)1097-0290(19980905)59:5&lt
[10]  
621::AID-BIT13&gt