Jójárt Balázs, Poša Mihalj, Fiser Béla, Szőri Milán, Farkaš Zita, Viskolcz Béla
Department of Chemical Informatics, Faculty of Education, University of Szeged, Szeged, Hungary.
Department of Pharmacy, Faculty of Medicine, University of Novi Sad, Novi Sad, Serbia.
PLoS One. 2014 Jul 8;9(7):e102114. doi: 10.1371/journal.pone.0102114. eCollection 2014.
Micellisation process for sodium dodecyl sulphate and sodium cholate in 1∶1 molar ratio was investigated in a combined approach, including several experimental methods and coarse grained molecular dynamics simulation. The critical micelle concentration (cmc) of mixed micelle was determined by spectrofluorimetric and surface tension measurements in the temperature range of 0-50°C and the values obtained agreed with each other within the statistical error of the measurements. In range of 0-25°C the cmc values obtained are temperature independent while cmc values were increased at higher temperature, which can be explained by the intensive motion of the monomers due to increased temperature. The evidence of existing synergistic effect among different constituent units of the micelle is indicated clearly by the interaction parameter (β1,2) calculated from cmc values according to Rubingh. As the results of the conductivity measurements showed the negative surface charges of the SDS-NaCA micelle are not neutralized by counterions. Applying a 10 µs long coarse-grained molecular dynamics simulation for system including 30-30 SDS and CA (with appropriate number of Na+ cations and water molecules) we obtained semi-quantitative agreement with the experimental results. Spontaneous aggregation of the surfactant molecules was obtained and the key steps of the micelle formation are identified: First a stable SDS core was formed and thereafter due to the entering CA molecules the size of the micelle increased and the SDS content decreased. In addition the size distribution and composition as well as the shape and structure of micelles are also discussed.
采用包括多种实验方法和粗粒度分子动力学模拟在内的综合方法,研究了摩尔比为1∶1的十二烷基硫酸钠和胆酸钠的胶束化过程。通过荧光光谱法和表面张力测量,在0 - 50°C的温度范围内测定了混合胶束的临界胶束浓度(cmc),所得值在测量的统计误差范围内相互吻合。在0 - 25°C范围内,所得的cmc值与温度无关,而在较高温度下cmc值增加,这可以用温度升高导致单体的剧烈运动来解释。根据鲁宾(Rubingh)方法从cmc值计算得到的相互作用参数(β1,2)清楚地表明了胶束不同组成单元之间存在协同效应。电导率测量结果表明,SDS-NaCA胶束的负表面电荷未被抗衡离子中和。对包含30 - 30个SDS和CA(以及适当数量的Na +阳离子和水分子)的系统进行了10微秒的粗粒度分子动力学模拟,我们得到了与实验结果的半定量一致性。获得了表面活性剂分子的自发聚集,并确定了胶束形成的关键步骤:首先形成稳定的SDS核心,此后由于CA分子的进入,胶束尺寸增大,SDS含量降低。此外,还讨论了胶束的尺寸分布、组成以及形状和结构。