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首页> 外文期刊>Journal of Applied Polymer Science >Permeation of mixtures of organic liquids through polymeric membranes: Role of liquid-liquid interactions
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Permeation of mixtures of organic liquids through polymeric membranes: Role of liquid-liquid interactions

机译:有机液体混合物透过聚合物膜的渗透:液-液相互作用的作用

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The permeation of pure organic liquids and mixtures of organic liquids through commercial butyl, neoprene, and nitrile membranes was studied using dynamic material deformation (swelling) and permeation techniques. The derived parameters, the breakthrough time (t(BT)), steady-state permeation rate (SSPR), and initial swelling rate (SR), show deviations from additivity for the mixtures, based on the parameters of the pure liquids on a mol fraction basis. In the majority of cases for the three membranes examined, the deviations are independent of the nature of the membranes, and the signs of the deviations for t(BT) are opposite to those for SSPR or SR, provided that the membranes are not degraded by one of the solvents. An approach that considers only solvent-solvent interactions based on the enthalpy of mixing was used to predict deviations for mixtures. For mixtures where the enthalpy of mixing is large and exothermic, the permeation of the mixture is less than expected, while for systems where the enthalpy of mixing is large and endothermic, the permeation is larger than expected. A simple semiempirical model predicts the sign and magnitude of the permeation of 73% of the system-permeation property combinations investigated, which show significant deviations from ideality. It is interesting to note that the wrong predictions are for systems where the predictions are positive, that is, for SSPR and SR rates with endothermic systems and for t(BT) with exothermic systems. The exceptions also seem to be for systems that correspond to materials having a high resistance to one of the solvents and a very low resistance to the other solvent. Examples of ternary-mixture permeation data are also given and show that, even if two of the pure components do not permeate through a membrane, the membrane will offer little protection if the third component shows a high affinity for the membrane and if the enthalpies of mixing of this component with the other liquids are endothermic. (C) 2002 Wiley Periodicals, Inc. [References: 31]
机译:使用动态材料变形(溶胀)和渗透技术研究了纯有机液体和有机液体混合物通过商用丁基,氯丁橡胶和腈膜的渗透性。根据纯液体在摩尔上的参数,得出的参数,穿透时间(t(BT)),稳态渗透率(SSPR)和初始溶胀率(SR),显示出与混合物加性的偏差。分数基础。在大多数情况下,对于所检查的三种膜,偏差与膜的性质无关,并且t(BT)的偏差征兆与SSPR或SR的征兆相反,但前提是该膜不会因溶剂之一。一种基于混合焓仅考虑溶剂-溶剂相互作用的方法被用来预测混合物的偏差。对于混合焓大且放热的混合物,混合物的渗透小于预期,而对于混合焓大且吸热的系统,渗透大于预期。一个简单的半经验模型可以预测所研究的系统渗透性组合中73%的渗透的符号和幅度,这表明与理想情况存在显着偏差。有趣的是,错误的预测是针对预测为正的系统,即吸热系统的SSPR和SR速率以及放热系统的t(BT)。对于对应于对一种溶剂具有高耐受性而对另一种溶剂具有极低耐受性的材料的系统,似乎也有例外。还给出了三元混合物渗透数据的实例,这些数据表明,即使其中两个纯组分没有渗透过膜,但如果第三个组分对膜具有很高的亲和力,并且三元混合物的焓也不能提供保护。该组分与其他液体的混合是吸热的。 (C)2002 Wiley Periodicals,Inc. [参考:31]

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