Importance of phase equilibria for understanding supercritical fluid environments

被引:51
作者
Arai, K [1 ]
Adschiri, T [1 ]
机构
[1] Tohoku Univ, Dept Chem Engn, Aoba Ku, Sendai, Miyagi 9808579, Japan
关键词
supercritical water; cellulose; hydrogenation; energy conversion; nuclear wastes;
D O I
10.1016/S0378-3812(99)00116-8
中图分类号
O414.1 [热力学];
学科分类号
摘要
In this work, several applications are reviewed and the importance of phase equilibria is discussed. In the reaction of cellulose in subcritical and supercritical water for producing chemicals, cellulose decomposes to form lower carbon number sugars, oligomers, and various acids. As conditions change from a subcritical reaction environment to a supercritical reaction environment, we observed a drastic change of the kinetic rate constant, which is thought to be the result of the cellulose-water system changing from a heterogeneous state to a homogeneous state. Diamond anvil cell measurements (DAC) are used to provide Visualization of phase changes in the cellulose-water system. In the reaction of polyethylene terephthalate (PET) in supercritical water for recycling, PET decomposes to form oligomers, ethylene glycol, and the monomer, terephthalic acid. The reaction kinetics for this polymer-water system is much slower and requires 10 min for 100% conversion vs. 50 ms for 100% conversion of cellulose. The reason is thought to be due to the number and type of reaction phases present in the system, that is, solid-fluid or liquid-fluid phases. In the hydrogenation of heavy oils for energy conversion applications, the reaction kinetics can be very slow. Supercritical water provides a homogeneous reaction environment for the hydrogen of heavy oil system. However, for this case, we have found that an excellent hydrogenating atmosphere can be made by addition of oxygen, which apparently provides active hydrogen from CO formed, through the water-gas shift reaction. In catalytic reactions of heavy oils, in-situ extraction of coke precursors is provided by the supercritical water environment. Further studies are reported on the oxidation of hydrocarbons. In the treatment of high-level liquid wastes from the nuclear industries, it is found that many metals can be removed from solution by raising the temperature and pressure of the aqueous solutions. These results are discussed in view of recent supercritical water metal oxide solubility and supercritical water density measurements. (C) 1999 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:673 / 684
页数:12
相关论文
共 32 条
[1]  
ABRAHAM MA, 1997, ACS S SERIES, V670
[2]   CATALYTIC HYDROTREATING FOR NITROGEN REMOVAL FROM COAL-TAR PITCH IN SUPERCRITICAL-FLUID [J].
ADSCHIRI, T ;
NAKADA, K ;
OGASAWARA, S ;
ARAI, K .
KAGAKU KOGAKU RONBUNSHU, 1994, 20 (06) :965-970
[3]   CATALYTIC REFORMING OF COAL-TAR PITCH IN SUPERCRITICAL FLUID [J].
ADSCHIRI, T ;
SUZUKI, T ;
ARAI, K .
FUEL, 1991, 70 (12) :1483-1484
[4]   RAPID AND CONTINUOUS HYDROTHERMAL CRYSTALLIZATION OF METAL-OXIDE PARTICLES IN SUPERCRITICAL WATER [J].
ADSCHIRI, T ;
KANAZAWA, K ;
ARAI, K .
JOURNAL OF THE AMERICAN CERAMIC SOCIETY, 1992, 75 (04) :1019-1022
[5]   RAPID AND CONTINUOUS HYDROTHERMAL SYNTHESIS OF BOEHMITE PARTICLES IN SUBCRITICAL AND SUPERCRITICAL WATER [J].
ADSCHIRI, T ;
KANAZAWA, K ;
ARAI, K .
JOURNAL OF THE AMERICAN CERAMIC SOCIETY, 1992, 75 (09) :2615-2618
[6]  
ADSCHIRI T, 1998, IN PRESS I EC RES
[7]  
ADSCHIRI T, 1997, 9 INT C COAL SCI, P1505
[8]  
ARAI K, 1997, 4 INT S SUP FLUIDS S
[9]  
BOBLETER O, 1994, J ANAL APPL PYROL, V17, P319
[10]   FLUID MIXTURES AT HIGH-PRESSURES .9. PHASE-SEPARATION AND CRITICAL PHENOMENA IN 23 (NORMAL-ALKANE + WATER) MIXTURES [J].
BRUNNER, E .
JOURNAL OF CHEMICAL THERMODYNAMICS, 1990, 22 (04) :335-353