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首页> 外文期刊>Journal of Chemical and Engineering Data: the ACS Journal for Data >Micellar Properties and Related Thermodynamic Parameters of Aqueous Anionic Surfactants in the Presence of Monohydric Alcohols
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Micellar Properties and Related Thermodynamic Parameters of Aqueous Anionic Surfactants in the Presence of Monohydric Alcohols

机译:一元醇存在下水性阴离子表面活性剂的胶束性质和相关热力学参数

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The effect of monohydric alcohols, (C7-C_(10)), on the micellar behavior of anionic surfactants, sodium dodecylsulfate (SDS) and sodium dodecylbenzene sulfonate (SDBS), was investigated using experimentally measured densities, p, speeds of sound, u, and specific conductivities, K, at various temperatures and atmospheric pressure. A number of thermodynamic parameters, like apparent molar volumes,Φ_v, partial molar volumes, Φ°_v; isentropic compressibility, k_s, and various thermodynamic parameters of micellization were calculated to elucidate the interactions prevailing in the studied aqueous surfactant- alcohol systems. The decrease in critical micelle concentration (cmc) on addition of an additive may be seen in terms of establishment of additional hydrophobic interactions between the hydrophobic part of the surfactant and additive molecules. It can be seen that ΔG_m~o, < 0 is weakly dependent on alcohol concentrations in aqueous surfactant solutions. Further, ~1H and ~(13)C NMR chemical shift measurements in micelle solutions containing above-mentioned alcohols have also been carried out. From ~1H and ~(13)C NMR spectra, it was concluded that the site for preferential solubilization of alcohol is close to the headgroup of the micelle. The trend observed in carbon chemical shifts may be attributed to the chain length of the added alcohols due to the strong ion-dipole interaction between the negatively charged SDS headgroup and the hydroxyl group of the alcohol.
机译:一氧化碳(C7-C_(10))对阴离子表面活性剂十二烷基硫酸钠(SDS)和十二烷基苯磺酸钠(SDBS)的胶束行为的影响,是通过实验测得的密度,p,声速,u ,以及在不同温度和大气压下的比电导率K。许多热力学参数,例如表观摩尔体积Φ_v,部分摩尔体积Φ°_v;计算出等熵可压缩性,k_s和胶束化的各种热力学参数,以阐明研究的水性表面活性剂-醇体系中普遍存在的相互作用。在表面活性剂的疏水部分和添加剂分子之间建立另外的疏水相互作用方面,可以看出添加添加剂时临界胶束浓度(cmc)的降低。可以看出,ΔG_m〜o,<0弱依赖于表面活性剂水溶液中的醇浓度。此外,还已经在含有上述醇的胶束溶液中进行了〜1H和〜(13)C NMR化学位移测量。从〜1H和〜(13)C NMR光谱可以得出结论,醇优先增溶的位点靠近胶束的头基。在碳化学位移中观察到的趋势可能归因于所加成的醇的链长,这是由于带负电荷的SDS头基与醇的羟基之间存在强烈的离子-偶极相互作用。

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