Direct observation of cellulose dissolution in subcritical and supercritical water over a wide range of water densities (550-1000 kg/m3)

被引:84
作者
Ogihara, Y [1 ]
Smith, RL [1 ]
Inomata, H [1 ]
Arai, K [1 ]
机构
[1] Tohoku Univ, Res Ctr Supercrit Fluid Technol, Aoba Ku, Sendai, Miyagi 9808579, Japan
关键词
biomass; cellulose; microreactor; supercritical water; visualization;
D O I
10.1007/s10570-005-9008-1
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
Direct observations of the heating of microcrystalline cellulose (230 DP) in water at temperatures up to 410 degrees C and at pressures up to 700 MPa were made with a batch-type microreactor. Cellulose particles were found to dissolve with water over temperatures ranging from 315 to 355 degrees C at high pressures. Dissolution temperatures depended on water density and decreased from about 350 degrees C at a water density of 560 kg/m(3) to a minimum of around 320 degrees C at a water density of 850 kg/m(3). At densities greater than 850 kg/m(3), the dissolution temperatures increased and reached a value of about 347 degrees C at 980 kg/m(3). The cellulose dissolution temperatures were independent of heating rates for values ranging from 10 to 17 degrees C/s. The low dependence of dissolution temperatures on the heating rates is strong evidence for simultaneous dissolution and reaction of the cellulose. Different phenomena occurred depending on water density. At low densities, particles turned transparent and seemed to dissolve into the aqueous phase from the surface. From 670 to 850 kg/m(3), the cellulose particles visibly swelled just before completely collapsing and dissolving into the aqueous phase. The swelling probably increased water accessibility and particle surface area and thus lead to the lower dissolution temperatures observed. From 850 to 1000 kg/m(3), the particles required longer times to dissolve and many fine brown-like particles were generated as the particles dissolved. FT-IR spectra of the residues were analyzed. Residues formed from heating cellulose at high densities still retained some cellulose character whereas those as low densities had little cellulose character, especially in the O-H stretching vibration region.
引用
收藏
页码:595 / 606
页数:12
相关论文
共 41 条
[11]   Phase behavior and reaction of polyethylene in supercritical water at pressures up to 2.6 GPa and temperatures up to 670°C [J].
Fang, Z ;
Smith, RL ;
Inomata, H ;
Arai, K .
JOURNAL OF SUPERCRITICAL FLUIDS, 2000, 16 (03) :207-216
[12]   Biomass conversions in subcritical and supercritical water: driving force, phase equilibria, and thermodynamic analysis [J].
Feng, W ;
van der Kooi, HJ ;
Arons, JDS .
CHEMICAL ENGINEERING AND PROCESSING-PROCESS INTENSIFICATION, 2004, 43 (12) :1459-1467
[13]   Phase equilibria for biomass conversion processes in subcritical and supercritical water [J].
Feng, W ;
van der Kooi, HJ ;
Arons, JD .
CHEMICAL ENGINEERING JOURNAL, 2004, 98 (1-2) :105-113
[14]  
FERNANDEZPRINI R, 1997, INT ASS PROPERTIES W
[15]   Hydrothermal conversion of municipal organic waste into resources [J].
Goto, M ;
Obuchi, R ;
Hiroshi, T ;
Sakaki, T ;
Shibata, M .
BIORESOURCE TECHNOLOGY, 2004, 93 (03) :279-284
[16]   Hydrogen bond and crystal deformation of cellulose in sub/super-critical water [J].
Ito, T ;
Hirata, Y ;
Sawa, F ;
Shirakawa, N .
JAPANESE JOURNAL OF APPLIED PHYSICS PART 1-REGULAR PAPERS SHORT NOTES & REVIEW PAPERS, 2002, 41 (09) :5809-5814
[17]   A comparison of liquid hot water and steam pretreatments of sugar cane bagasse for bioconversion to ethanol [J].
Laser, M ;
Schulman, D ;
Allen, SG ;
Lichwa, J ;
Antal, MJ ;
Lynd, LR .
BIORESOURCE TECHNOLOGY, 2002, 81 (01) :33-44
[18]   THE ROLE OF DEOXYHEXONIC ACIDS IN THE HYDROTHERMAL DECARBOXYLATION OF CARBOHYDRATES [J].
LUIJKX, GCA ;
VANRANTWIJK, F ;
VANBEKKUM, H ;
ANTAL, MJ .
CARBOHYDRATE RESEARCH, 1995, 272 (02) :191-202
[19]   Roughening transition of prism faces of ice crystals grown from melt under pressure [J].
Maruyama, M .
JOURNAL OF CRYSTAL GROWTH, 2005, 275 (3-4) :598-605
[20]   Microscopy and calorimetry as complementary techniques to analyze sugar crystallization from amorphous systems [J].
Mazzobre, MF ;
Aguilera, JM ;
Buera, MP .
CARBOHYDRATE RESEARCH, 2003, 338 (06) :541-548