Determination and prediction of solid-liquid phase equilibrium for quaternary system of terephthalic acid plus isophthalic acid plus phthalic acid plus N-methyl-2-pyrrolidone at 303.15 K and 313.15 K

被引:22
作者
Du, Cun Bin [1 ]
Han, Shuo [1 ]
Zhong, Yun Hao [2 ]
Yao, Gan Bing [1 ]
Wang, Jian [1 ]
Zhao, Hongkun [1 ]
机构
[1] Yang Zhou Univ, Coll Chem & Chem Engn, Yangzhou 225002, Jiangsu, Peoples R China
[2] Nanjing Tech Univ, Overseas Educ Coll, Nanjing 225002, Jiangsu, Peoples R China
基金
中国国家自然科学基金;
关键词
Solid-liquid phase equilibrium; Phase diagram; Phthalic acid; Isophthalic acid; Terephthalic acid; N-methyl-2-pyrrolidone; SOLUBILITIES; N; N-DIMETHYLFORMAMIDE; CRYSTALLIZATION; SEPARATION; MIXTURE; CRESOL; WATER; SOLVENTS; ALCOHOL; DIAGRAM;
D O I
10.1016/j.fluid.2015.03.042
中图分类号
O414.1 [热力学];
学科分类号
摘要
Solid-liquid phase equilibrium and solubility data for quaternary system of terephthalic acid + isophthalic acid + phthalic acid + N-methyl-2-pyrrolidone at 303.15 K and 313.15 K were determined by Schreinemakers' method of wet residue under atmosphere pressure. Based on the measured solubility, the quaternary phase diagrams were constructed at the two studied temperatures according to the Janeck method. At each temperature, the quaternary phase diagram includes three crystallization regions of pure solid, three co-saturated curves and one eutectic point. The three pure solids are phthalic acid, adduct of isophthalic acid with N-methyl-2-pyrrolidone (the mole ratio of isophthalic acid to N-methyl-2-pyrrolidone is 1:2), adduct of terephthalic acid with N-methyl-2-pyrrolidone (the mole ratio of terephthalic acid to N-methyl-2-pyrrolidone is 1:2), which are confirmed by the method of Schreinemakers' wet residue. The crystallization region of adduct of terephthalic acid with N-methy12-pyrrolidone is larger than those of phthalic acid and adduct of isophthalic acid with N-methyl-2pyrrolidone. Furthermore, the quaternary solid-liquid phase equilibrium were predicted by NRTL model. The calculated quaternary phase diagrams agreed well with experimental data. (C) 2015 Elsevier B.V. All rights reserved.
引用
收藏
页码:103 / 110
页数:8
相关论文
共 30 条
[1]   Solubilities of Terephthalic Acid, Phthalic Acid, and Isophthalic Acid in Tetrahydrofuran, Cyclohexanone, 1,2-Diethoxyethane, and Acetophenone [J].
Che, Yao-Kun ;
Qu, Yi-Xin ;
Wang, Shui .
JOURNAL OF CHEMICAL AND ENGINEERING DATA, 2009, 54 (11) :3130-3132
[2]  
Cheng Y.W., 2008, CN Patent, Patent No. 101302152
[3]   Thermodynamic Study on the Adduct Crystallization of Terephthalic Acid with Amides [J].
Cheng Youwei ;
Peng Ge ;
Wu Bianhua ;
Guo Xia ;
Li Xi .
JOURNAL OF CHEMICAL AND ENGINEERING DATA, 2011, 56 (04) :1020-1024
[4]   Solubilities of m-phthalic acid in petroleum ether and its binary solvent mixture of alcohol plus petroleum ether [J].
Ding, Zhongwei ;
Zhang, Rongrong ;
Long, Bingwen ;
Liu, Liying ;
Tu, Haifeng .
FLUID PHASE EQUILIBRIA, 2010, 292 (1-2) :96-103
[5]   SEPARATION OF CLOSE BOILING-POINT MIXTURES (P-CRESOL/M-CRESOL, GUAIACOL/ALKYLPHENOLS, 3-PICOLINE/4-PICOLINE, SUBSTITUTED ANILINES) THROUGH DISSOCIATION EXTRACTIVE CRYSTALLIZATION [J].
GAIKAR, VG ;
MAHAPATRA, A ;
SHARMA, MM .
INDUSTRIAL & ENGINEERING CHEMISTRY RESEARCH, 1989, 28 (02) :199-204
[6]  
Gray J.S., 2013, CN Patent, Patent No. [103,124,714, 103124714]
[7]   Solubility of terephthalic acid in aqueous N-methyl pyrrolidone and N,N-dimethyl acetamide solvents at (303.2 to 363.2) K [J].
Guo, Xia ;
Cheng, You-wei ;
Wang, Li-jun ;
Li, Xi .
JOURNAL OF CHEMICAL AND ENGINEERING DATA, 2008, 53 (07) :1421-1423
[8]   SEPARATION OF PHENOL FROM ITS MIXTURE WITH ORTHO-CRESOL BY ADDUCTIVE CRYSTALLIZATION [J].
JADHAV, VK ;
CHIVATE, MR ;
TAVARE, NS .
JOURNAL OF CHEMICAL AND ENGINEERING DATA, 1992, 37 (02) :232-235
[9]   Solid-Liquid Phase Equilibrium for the Ternary System 3-Chlorophthalic Acid+4-Chlorophthalic Acid plus Water at (283.15 and 313.15) K [J].
Ji, Hai-Zhe ;
Meng, Xian-Chao ;
Zhao, Hong-Kun .
JOURNAL OF CHEMICAL AND ENGINEERING DATA, 2010, 55 (09) :4013-4015
[10]   KINETIC-STUDY ON THIOUREA ADDUCTION WITH CYCLOHEXANE-METHYLCYCLOPENTANE SYSTEM .1. EQUILIBRIUM STUDY [J].
KIM, KJ ;
LEE, CH ;
RYU, SK .
INDUSTRIAL & ENGINEERING CHEMISTRY RESEARCH, 1994, 33 (01) :118-124