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以1-丁醇和1-戊醇为助表面活性剂、正庚烷和正癸烷为油相的混合表面活性剂(十六烷基三甲基溴化铵和Brij-58)形成的水包油型微乳液的相行为、界面组成和热力学性质

Phase behavior, interfacial composition and thermodynamic properties of mixed surfactant (CTAB and Brij-58) derived w/o microemulsions with 1-butanol and 1-pentanol as cosurfactants and n-heptane and n-decane as oils.

作者信息

Mitra Rajib K, Paul Bidyut K, Moulik Satya P

机构信息

Colloid and Surface Science Group, Geological Studies Unit, Indian Statistical Institute, Kolkata 700108, India.

出版信息

J Colloid Interface Sci. 2006 Aug 15;300(2):755-64. doi: 10.1016/j.jcis.2006.04.011. Epub 2006 Apr 7.

DOI:10.1016/j.jcis.2006.04.011
PMID:16677663
Abstract

Phase diagrams of pseudo-quaternary systems of cetyltrimethylammonium bromide (CTAB)/polyoxyethylene(20)cetyl ether (Brij-58)/water/1-butanol (or 1-pentanol)/n-heptane (or n-decane) at fixed omega (=[water]/[surfactant]) of 55.6 were constructed at different temperatures (293, 303, 313, and 323 K) and different mole fraction compositions of Brij-58 (X(Brij-58)=0, 0.5, and 1.0 in CTAB + Brij-58 mixture). Pure CTAB stabilized systems produced larger single-phase domains than pure Brij-58 stabilized systems. Increasing temperature increased the single-phase domain in the Brij-58 stabilized systems, whereas the domain decreased in the CTAB stabilized systems. For mixed surfactant systems (with X(Brij)=0.5) negligible influence of temperature in the studied range of 293 to 323 K on the phase behavior was observed. Interfacial compositions of the mixed microemulsion systems at different temperature and different compositions were evaluated by the dilution method. The n(a)(i) (number of moles of alcohol at the interface) and n(a)(o) (number of moles of alcohol in the oil phase) determined from dilution experiments were found to decrease and increase respectively for CTAB stabilized systems, whereas an opposite trend was witnessed for Brij-58 stabilized systems. The energetics of transfer of cosurfactants from oil to the interface were found to be exothermic and endothermic for CTAB and Brij-58 stabilized systems, respectively. At equimolar composition of CTAB and Brij-58, the phase diagrams were temperature insensitive, so that the enthalpy of the aforesaid transfer process was zero.

摘要

在固定的ω(=[水]/[表面活性剂])为55.6的条件下,构建了十六烷基三甲基溴化铵(CTAB)/聚氧乙烯(20)十六烷基醚(Brij - 58)/水/1 - 丁醇(或1 - 戊醇)/正庚烷(或正癸烷)的拟四元体系相图,实验温度范围为293、303、313和323 K,且Brij - 58在CTAB + Brij - 58混合物中的摩尔分数组成不同(X(Brij - 58)=0、0.5和1.0)。与纯Brij - 58稳定体系相比,纯CTAB稳定体系产生的单相区更大。升高温度会使Brij - 58稳定体系中的单相区增大,而CTAB稳定体系中的单相区减小。对于混合表面活性剂体系(X(Brij)=0.5),在293至323 K的研究温度范围内,观察到温度对相行为的影响可忽略不计。采用稀释法评估了不同温度和不同组成的混合微乳液体系的界面组成。稀释实验测定的CTAB稳定体系中,界面处醇的摩尔数n(a)(i)和油相中醇的摩尔数n(a)(o)分别减小和增大,而Brij - 58稳定体系则呈现相反趋势。对于CTAB和Brij - 58稳定体系,助表面活性剂从油相转移至界面的能量变化分别为放热和吸热。在CTAB和Brij - 58等摩尔组成时,相图对温度不敏感,因此上述转移过程的焓为零。

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