标题:Liquid-liquid extraction of methanol from its mixtures with hexane using three imidazolium-based ionic liquids
作者:Zhu, Zhaoyou; Bai, Wenting; Xu, Ying; Gong, Huaizheng; Wang, Yinglong; Xu, Dongmei; Gao, Jun
作者机构:[Zhu, Zhaoyou; Bai, Wenting; Xu, Ying; Wang, Yinglong] Qingdao Univ Sci & Technol, Coll Chem Engn, Qingdao 266042, Shandong, Peoples R China.; [Gong 更多
通讯作者:Wang, YL;Wang, Yinglong
通讯作者地址:[Wang, YL]Qingdao Univ Sci & Technol, Coll Chem Engn, Qingdao 266042, Shandong, Peoples R China.
来源:JOURNAL OF CHEMICAL THERMODYNAMICS
出版年:2019
卷:138
页码:189-195
DOI:10.1016/j.jct.2019.06.024
关键词:Ionic liquids; Liquid-liquid equilibrium; N-hexane; Methanol; NRTL;; UNIQUAC
摘要:N-hexane plays a significant role in the industrial manufacturing process of methanol. The separation of n-hexane and methanol is important and difficult due to the azeotropic phenomenon. The objective of this work is to measure the experimental data for the three ternary systems n-hexane + methanol + ionic liquids (1-butyl-3-methylimidazolium bis(trifluoromethanesulfonyl), 1-decyl-3-methylimidazolium bis (trifluoromethylsulfonyl)amide and 1-butyl-3-methylimidazolium hexafluorophosphate) at T = 298.15 K and 101.3 kPa. The COSMO-SAC model was used to calculate the infinite dilution activity coefficients of the eleven ILs in the work and in the literature. The liquid-liquid equilibrium data for the ternary systems were compared with the calculated values obtained using the non-random two liquid and universal quasi-chemical activity models, and the binary interaction parameters of the two models were obtained by regressing the experimental data. Comparing the values of the distribution coefficients and separation factors of the three ILs, 1-decyl-3-methylimidazolium bis(trifluoromethylsul fonyl) amide showed the best extraction effect. The influence of the alkyl chain length and different anions on the liquid-liquid equilibrium data was discussed. (C) 2019 Elsevier Ltd.
收录类别:EI;SCOPUS;SCIE
资源类型:期刊论文
原文链接:https://www.scopus.com/inward/record.uri?eid=2-s2.0-85067655725&doi=10.1016%2fj.jct.2019.06.024&partnerID=40&md5=176a1d2291678285e7f47b158f9121c2
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