Extraction of methylcyclohexane−toluene mixture using imidazolium ionic liquids

Elena Graczová , Dávid Molnár , Pavol Steltenpohl , Karel Řehák
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Abstract

Separation of aromatics from non-aromatic hydrocarbons was exemplified assuming the liquid-phase extraction process for methylcyclohexane−toluene model mixture separation using the newly tested 1-ethyl-3-methylimidazolium bis(trifluoromethylsulfonyl)imide ([EMim][NTf2]) ionic liquid (IL). For this process a separation unit was proposed consisting of separation part represented by a counter-current extraction column and regeneration part including a vacuum evaporator and a vacuum distillation column. Separation of feed composed of 10 mole% of toluene in methylcyclohexane was considered in the designed separation unit. Designed separation efficiency of the unit was based on the following specifications: minimum methylcyclohexane and toluene content in the product streams of 99.5 mole% and the purity of regenerated extraction solvent recycled to the extraction column above 99 mole%.

Mathematical model of a counter-current extractor was compiled and its operation was simulated in the Matlab environment. In extractor simulations, proprietary phase equilibrium data were employed. Ternary liquid–liquid equilibrium (LLE) of the methylcyclohexane−toluene−[EMim][NTf2] system was estimated experimentally, from which the model parameters of the original NRTL equation were evauated and used for the ternary phase equilibrium description.

Aspen Plus was used to design a separation unit for the title hydrocarbons mixture separation, including the extraction solvent regeneration. Simulation of the proposed separation unit operation was focused not only on its separation efficiency but also on the evaluation of the unit energetic requirements.

Results of the unit design calculations (parameters of individual equipment, heat duties) obtained for the tested ionic liquid [EMim][NTf2] were confronted with the simulation results obtained for two ILs recommended in the literature for the non-aromatic–aromatic hydrocarbon mixture separation, namely 1‑butyl‑3-methylimidazolium tetracyanoborate [BMim][TCB] and 1-hexyl-3-methylimidazolium tetracyanoborate [HMim][TCB]. Based on the energetic analysis, the heat integration of the suggested separation unit was carried out for ionic liquid [HMim][TCB], which appeared to be the most efficient extraction solvent among those tested in this study, The heat integration resulted in about 71% reduction of the heat demand of the proposed separation unit.

咪唑离子液体萃取甲基环己烷-甲苯混合物
假设使用新测试的1-乙基-3-甲基咪唑鎓双(三氟甲基磺酰基)酰亚胺([EMim][NTf2])离子液体(IL)进行甲基环己烷−甲苯模型混合物分离的液相萃取工艺,举例说明了芳烃与非芳烃的分离。对于该工艺,提出了一种分离单元,该分离单元由逆流萃取塔代表的分离部分和包括真空蒸发器和真空蒸馏塔的再生部分组成。在设计的分离装置中考虑了由10摩尔%甲苯在甲基环己烷中组成的进料的分离。该装置的设计分离效率基于以下规范:产物流中甲基环己烷和甲苯的最低含量为99.5摩尔%,回收到萃取柱的再生萃取溶剂的纯度为99摩尔%以上。编制了逆流萃取器的数学模型,并在Matlab环境中对其运行进行了模拟。在提取器模拟中,采用了专有的相平衡数据。实验估计了甲基环己烷-甲苯−[EMim][NTf2]体系的三元液-液平衡(LLE),从中推导出了原始NRTL方程的模型参数,并用于三元相平衡描述。Aspen Plus用于设计用于标题烃混合物分离的分离装置,包括萃取溶剂再生。对所提出的分离装置运行的模拟不仅关注其分离效率,还关注对装置能量需求的评估。测试离子液体[EMim][NTf2]获得的单元设计计算结果(单个设备的参数、热负荷)与文献中推荐的非芳烃-芳烃混合物分离的两种离子液体的模拟结果相一致,即1-丁基-3-甲基咪唑四氰基硼酸盐[BMim][TCB]和1-己基-3-甲基咪唑四氰基硼化物[HMim][TCB]。基于能量分析,对离子液体[HMim][TCB]进行了所建议的分离单元的热整合,离子液体[HMim][TCB]似乎是本研究中测试的最有效的萃取溶剂。热整合使所建议的分离器的热需求减少了约71%。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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