Measurement and correlation of the solid-liquid-gas equilibria for carbon dioxide plus normal chain saturated aliphatic hydrocarbon systems

被引:13
作者
Uchida, Hirohisa [1 ]
Kamijo, Tetsuo [1 ]
机构
[1] Shinshu Univ, Fac Engn, Dept Chem & Mat Engn, Nagano 3808553, Japan
关键词
Solid-liquid-gas (S-L-G) equilibria; Carbon dioxide; Tetradecanoic acid; Hexadecanoic acid; 1-Hexadecanol; X SPACE MODEL; PRESSURE PHASE-EQUILIBRIA; MELTING-POINT DEPRESSION; BINARY-SYSTEMS; SUPERCRITICAL FLUIDS; ETHYLENE-NAPHTHALENE; RAPID EXPANSION; THERMODYNAMIC ANALYSIS; MICRONIZATION; BEHAVIOR;
D O I
10.1016/j.supflu.2009.08.007
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
The pressure p-temperature T projections of solid-liquid-gas (S-L-G) three-phase coexistence lines for the carbon dioxide + tetradecanoic acid (C14H28O2) system, the carbon dioxide + hexadecanoic acid (C16H34O2) system, and the carbon dioxide + 1-hexadecanol (C16H34O) were measured by the first melting point method in which the initial appearance of the liquid phase was observed. The profiles of the p-T projections of the S-L-G lines for the carbon dioxide + acid systems are similar to each other, the S-L-G equilibria for the carbon dioxide + acid systems are, however, different from that for the carbon dioxide + 1-hexadecanol systems. The experimental p-T projections of the S-L-G lines were also correlated by the Peng-Robinson equation of state and the van der Waals type mixing rules with two binary interaction parameters introduced into attraction term and size terms, respectively. The present model gave good correlation results for all of the experimental S-L-G lines with maximum average absolute relative deviations of 0.075% for the carbon dioxide + tetradecanoic acid system, 0.14% for the carbon dioxide + hexadecanoic acid system and 0.28% for the carbon dioxide + 1-hexadecanol system, respectively. (C) 2009 Elsevier B.V. All rights reserved.
引用
收藏
页码:136 / 141
页数:6
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