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Ternary Liquid–Liquid Equilibria for Mixtures of {Ionic Liquid + Thiophene or Benzothiophene + Heptane} at T = 308.15 K

机译:{离子液体+噻吩或苯并噻吩+庚烷}的混合物在T = 308.15 K时的三元液-液平衡

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摘要

In this work, the desulfurization ability of alkyl-piperidinium-based and phosphonium-based ionic liquids (ILs) for (thiophene or benzothiophene + heptane) mixtures are studied. With this aim, ternary liquid–liquid phase equilibrium data (LLE) have been obtained for mixtures of {IL (1) + thiophene, or benzothiophene (2) + heptane (3)} at T = 308.15 K and p = 101.33 kPa. For this study 1-pentyl-1-methylpiperidinium bis{(trifluoromethyl)sulfonyl}imide, [C1C5PIP][NTf2], and tributylethylphosphonium diethylphosphate, [P2,4,4,4][DEP], were used. The suitability of these ILs as solvents for extractive desulfurization has been evaluated in terms of the solute distribution ratio and selectivity. Immiscibility was observed in the binary liquid systems of (thiophene, or benzothiophene + heptane) with both ILs. One of the studied ILs, [C1C5PIP][NTf2], shows high distribution ratios and high selectivities for extraction of sulfur compounds. The data obtained have been correlated with the non-random two liquid NRTL model. The experimental tie-lines and the phase compositions in mole fractions in the ternary systems were calculated with an average root mean square deviation of 0.0052.Electronic supplementary materialThe online version of this article (doi:10.1007/s10953-014-0276-y) contains supplementary material, which is available to authorized users.
机译:在这项工作中,研究了烷基哌啶基和phospho基离子液体(IL)对(噻吩或苯并噻吩+庚烷)混合物的脱硫能力。为此,已获得{IL(1)+噻吩或苯并噻吩(2)+庚烷(3)}的混合物的三元液相平衡数据(LLE),T = 308.15 K,p = 101.33 kPa。在这项研究中,使用了双{((三氟甲基)磺酰基}酰亚胺的1-戊基-1-甲基哌啶[C1C5PIP] [NTf2]和磷酸二乙基三丁基乙基phosph [P2,4,4,4] [DEP]。这些溶质作为萃取脱硫溶剂的适用性已通过溶质分布比和选择性进行了评估。在两个IL的二元液体系统(噻吩或苯并噻吩+庚烷)中均观察到不溶混。所研究的IL之一是[C1C5PIP] [NTf2],显示出高的分配比和高的选择性,可萃取硫化合物。获得的数据已与非随机两种液体NRTL模型相关。计算出三元体系中的实验联系线和摩尔分数的相组成,平均均方根偏差为0.0052。电子补充材料本文的在线版本(doi:10.1007 / s10953-014-0276-y)包含补充材料,授权用户可以使用。

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