Model for estimating activity coefficients in binary and ternary ionic surfactant solutions

IF 3 4区 地球科学 Q2 ENVIRONMENTAL SCIENCES Journal of Atmospheric Chemistry Pub Date : 2020-11-07 DOI:10.1007/s10874-020-09407-4
Silvia M. Calderón, Jussi Malila, Nønne L. Prisle
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引用次数: 6

Abstract

We introduce the CMC based Ionic Surfactant Activity model (CISA) to calculate activity coefficients in ternary aqueous solutions of an ionic surfactant and an inorganic salt. The surfactant can be either anionic or cationic and in the present development, the surfactant and inorganic salts share a common counterion. CISA incorporates micellization into the Pitzer–Debye–Hückel (PDH) framework for activities of mixed electrolyte solutions. To reduce computing requirements, a parametrization of the critical micelle concentration (CMC) is used to estimate the degree of micellization instead of explicit equilibrium calculations. For both binary and ternary systems, CISA only requires binary experimentally-based parameters to describe water–ion interactions and temperature–composition dependency of the CMC. The CISA model is intended in particular for atmospheric applications, where higher-order solution interaction parameters are typically not constrained by experiments and the description must be reliable across a wide range of compositions. We evaluate the model against experimental activity data for binary aqueous solutions of ionic surfactants sodium octanoate and sodium decanoate, as common components of atmospheric aerosols, and sodium dodecylsulfate, the most commonly used model compound for atmospheric surfactants. Capabilities of the CISA model to describe ternary systems are tested for the water–sodium decanoate–sodium chloride system, a common surrogate for marine background cloud condensation nuclei and to our knowledge the only atmospherically relevant system for which ternary activity data is available. For these systems, CISA is able to provide continuous predictions of activity coefficients both below and above CMC and in all cases gives an improved description of the water activity above the CMC, compared to the alternative model of Burchfield and Wolley [J. Phys. Chem., 88(10), 2149–2155 (1984)]. The water activity is a key parameter governing the formation and equilibrium growth of cloud droplets. The CISA model can be extended from the current form to include the effect of other inorganic salts with the existing database of binary PDH parameters and using appropriate mixing rules to account for ion specificity in the micellization process.

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二元和三元离子表面活性剂溶液活度系数估算模型
介绍了基于CMC的离子表面活性剂活度模型(CISA),用于计算离子表面活性剂与无机盐三元水溶液的活度系数。表面活性剂可以是阴离子或阳离子,在目前的发展中,表面活性剂和无机盐有一个共同的反离子。CISA将胶束结合到混合电解质溶液活性的pitzer - debye - h ckel (PDH)框架中。为了减少计算需求,临界胶束浓度(CMC)的参数化被用来估计胶束化程度,而不是显式的平衡计算。对于二元和三元体系,CISA只需要二元实验参数来描述CMC的水-离子相互作用和温度-组成依赖性。CISA模型特别适用于大气应用,在大气应用中,高阶溶液相互作用参数通常不受实验的限制,并且描述必须在广泛的成分范围内可靠。我们对离子表面活性剂辛酸钠和癸酸钠(作为大气气溶胶的常见成分)和十二烷基硫酸钠(最常用的大气表面活性剂模型化合物)二元水溶液的实验活性数据进行了模型评估。CISA模型描述三元系统的能力在水-癸酸钠-氯化钠系统中进行了测试,该系统是海洋背景云凝结核的常用替代品,据我们所知,它是唯一可获得三元活动数据的大气相关系统。与Burchfield和Wolley的替代模型相比,对于这些系统,CISA能够提供CMC以下和CMC以上活度系数的连续预测,并且在所有情况下都能更好地描述CMC以上的水活度。理论物理。化学。[j].农业科学,88(10),2149-2155(1984)。水活度是控制云滴形成和平衡生长的关键参数。CISA模型可以从现有的形式扩展到包括其他无机盐的影响,并使用现有的二元PDH参数数据库,并使用适当的混合规则来考虑胶束过程中的离子特异性。
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来源期刊
Journal of Atmospheric Chemistry
Journal of Atmospheric Chemistry 地学-环境科学
CiteScore
4.60
自引率
5.00%
发文量
16
审稿时长
7.5 months
期刊介绍: The Journal of Atmospheric Chemistry is devoted to the study of the chemistry of the Earth''s atmosphere, the emphasis being laid on the region below about 100 km. The strongly interdisciplinary nature of atmospheric chemistry means that it embraces a great variety of sciences, but the journal concentrates on the following topics: Observational, interpretative and modelling studies of the composition of air and precipitation and the physiochemical processes in the Earth''s atmosphere, excluding air pollution problems of local importance only. The role of the atmosphere in biogeochemical cycles; the chemical interaction of the oceans, land surface and biosphere with the atmosphere. Laboratory studies of the mechanics in homogeneous and heterogeneous transformation processes in the atmosphere. Descriptions of major advances in instrumentation developed for the measurement of atmospheric composition and chemical properties.
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