首页> 外文期刊>Journal of Colloid and Interface Science >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
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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

机译:以1-丁醇和1-戊醇为辅助表面活性剂,以正庚烷和正癸烷为油的不带微乳液的混合表面活性剂(CTAB和Brij-58)衍生的相行为,界面组成和热力学性质

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摘要

Phase diagrams of pseudo-quaternary systems of cetyltrimethylammonium bromide (CTAB)/polyoxyethylene(20)cetyl ether (Brij-58)/water/1-butanol (or 1-pentanol)-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.
机译: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)的拟季铵盐体系的相图(= [水] / [表面活性剂])在不同温度(293,303,313和323 K)和Brij-58(X_(Brij)-58 = 0,0.5,和1.0在CTAB + Brij-58混合物)。纯的CTAB稳定系统比纯Brij-58稳定系统产生更大的单相畴。温度升高使Brij-58稳定系统的单相畴增大,而CTAB稳定系统的畴减小。对于X_(Brij)-0.5的混合表面活性剂体系,观察到的温度在293至323 K范围内对相行为的影响可忽略不计。稀释法n_a〜i(酒精摩尔数通过稀释实验确定的CTAB稳定体系的n)和油中醇的摩尔数n_a〜o分别降低和增加,而Brij-58稳定体系的趋势则相反。发现辅助表面活性剂从油到界面的转移分别对于CTAB和Brij-58稳定系统是放热的和吸热的。在CTAB和Brij-58的等摩尔组成下,相图对温度不敏感,因此焓上述转移过程为零。

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