Interfacial tensions of ethanol-carbon dioxide and ethanol-nitrogen. Dependence of the interfacial tension on the fluid density - prerequisites and physical reasoning

被引:41
作者
Dittmar, D [1 ]
Fredenhagen, A [1 ]
Oei, SB [1 ]
Eggers, R [1 ]
机构
[1] Tech Univ Hamburg, Dept Thermal Separat Proc Heat & Mass Transfer, D-21073 Hamburg, Germany
关键词
interface; supercritical fluid; interfacial tension; concept; theory;
D O I
10.1016/S0009-2509(02)00626-7
中图分类号
TQ [化学工业];
学科分类号
0817 ;
摘要
Interfacial tensions in the systems ethanol-carbon dioxide and ethanol nitrogen are measured. In both systems the interfacial tension decreases with increasing pressure. The interfacial tension in the system ethanol-nitrogen decreases with increasing temperature. In contrast to this, in the system ethanol-carbon dioxide at high pressures an isobaric increase in temperature provokes an increase in interfacial tension. In the system ethanol-carbon dioxide at elevated pressure the density of the carbon dioxide phase is the only influence parameter concerning the interfacial tension. This phenomena can be observed for various other systems with one near critical or supercritical component and a high solubility of this component in the liquid phase and at temperatures above the critical temperature of the gas. For this fact a physical reasoning, which is based on a new concept of partial interfacial tensions, is given. Furthermore, it is stated that the interfacial tension of fatty systems in contact with carbon dioxide has approximately the same dependence on the reduced density (p(r) = p/p(c)) of the supercritical phase as the interfacial tension of the same systems in contact with ethane. The knowledge of this fact can help to avoid experiments with ethane, which is flammable. (C) 2003 Elsevier Science Ltd. All rights reserved.
引用
收藏
页码:1223 / 1233
页数:11
相关论文
共 46 条
[31]   Investigating the stability of falling films at round vertical film carriers under high pressure [J].
Moser, M ;
Trepp, C .
CHEMICAL ENGINEERING & TECHNOLOGY, 1997, 20 (09) :612-616
[32]   EQUILIBRIUM PHASE COMPOSITIONS, PHASE DENSITIES, AND INTERFACIAL-TENSIONS FOR CO2 + HYDROCARBON SYSTEMS .2. CO2 + NORMAL-DECANE [J].
NAGARAJAN, N ;
ROBINSON, RL .
JOURNAL OF CHEMICAL AND ENGINEERING DATA, 1986, 31 (02) :168-171
[33]  
Oei SB, 2001, CHEM-ING-TECH, V73, P830, DOI 10.1002/1522-2640(200107)73:7<830::AID-CITE830>3.0.CO
[34]  
2-7
[35]  
Rabinovich V.A., 1988, Thermophysical Properties of Neon, Argon, Krypton, and Xenon
[36]   Interfacial Tension of (CO2+CH4) plus water from 298 K to 373 K and pressures up to 30 MPa [J].
Ren, QY ;
Chen, GJ ;
Yan, W ;
Guo, TM .
JOURNAL OF CHEMICAL AND ENGINEERING DATA, 2000, 45 (04) :610-612
[37]  
Rusanov AI, 1978, PHASENGLEICHGEWICHTE
[38]  
SCHIEMANN H, 1993, THESIS U ERLANGEN NU
[39]   A new equation of state for carbon dioxide covering the fluid region from the triple-point temperature to 1100 K at pressures up to 800 MPa [J].
Span, R ;
Wagner, W .
JOURNAL OF PHYSICAL AND CHEMICAL REFERENCE DATA, 1996, 25 (06) :1509-1596
[40]  
Sychev V.V., 1987, Thermodynamic Properties of Ethane