Löf David, Tomsic Matija, Glatter Otto, Fritz-Popovski Gerhard, Schillén Karin
Division of Physical Chemistry, Center for Chemistry and Chemical Engineering, P.O. Box 124, Lund University, SE-22100 Lund, Sweden.
J Phys Chem B. 2009 Apr 23;113(16):5478-86. doi: 10.1021/jp808442d.
A structural characterization of mixed micelles formed in aqueous solution by the PEO-PPO-PEO triblock copolymer P123 and the nonionic surfactant C(12)EO(6) was carried out using various techniques, including ultralow shear viscosimetry, depolarized dynamic light scattering (VH-DLS), depolarized static light scattering (VH-SLS), and small-angle X-ray scattering (SAXS). The sphere-to-rod transition of the mixed micelles was studied in a diluted regime (P123 concentrations ranging from 0.5 to 10 wt %) at C(12)EO(6)/P123 molar ratios of 2.2, 3.2, 6.0, and 11 as well as for the pure C(12)EO(6). The data from VH-SLS and viscosimetry displayed a sharp increase in the intensity and viscosity, respectively, at the sphere-to-rod transition, and the results from the two methods were in accordance. In both techniques, an increased transition temperature with increasing content of C(12)EO(6) (in the molar ratio regime from 2.2 to 11) was observed. SAXS was used as the main technique, and a thorough structural characterization was performed, where indirect Fourier transformation (IFT) and generalized indirect Fourier transformation (GIFT) were employed in the analysis procedure of the SAXS data. The p(r) functions obtained from the IFT (employed at low P123 concentrations, i.e., 1.0 and 2.0 wt %) and GIFT (employed above 2.0 wt %) analyses revealed increased inhomogeneities in the mixed micelles when the molar ratio was increased. This suggested that the C(12)EO(6) organized themselves at the interface between the PPO core and the PEO corona of the P123 micelles, with the C(12) alkyl chain stretching into the hydrophobic core and the EO(6) part residing in the hydrophilic corona. The structure factor parameters obtained with GIFT for a molar ratio of 2.2 at a P123 concentration of 5.0 wt % showed radius values smaller than what was estimated from the p(r) functions. This was explained by an interpenetration of the PEO chains from one mixed micelle into a neighboring one. VH-DLS was performed on the mixed micelles at a temperature 3 degrees C above the transition temperature and at a molar ratio of 2.2. From the analyzed data, the average length L of the rods was estimated to be 102 nm.
使用多种技术对聚环氧乙烷-聚环氧丙烷-聚环氧乙烷三嵌段共聚物P123和非离子表面活性剂C(12)EO(6)在水溶液中形成的混合胶束进行了结构表征,这些技术包括超低剪切粘度测定法、去偏振动态光散射(VH-DLS)、去偏振静态光散射(VH-SLS)和小角X射线散射(SAXS)。在稀释体系(P123浓度范围为0.5至10 wt%)中,研究了C(12)EO(6)/P123摩尔比为2.2、3.2、6.0和11以及纯C(12)EO(6)时混合胶束从球形到棒状的转变。VH-SLS和粘度测定法的数据分别显示,在从球形到棒状的转变处强度和粘度急剧增加,两种方法的结果一致。在这两种技术中,均观察到随着C(12)EO(6)含量增加(摩尔比范围为2.2至11)转变温度升高。SAXS被用作主要技术,并进行了全面的结构表征,在SAXS数据分析过程中采用了间接傅里叶变换(IFT)和广义间接傅里叶变换(GIFT)。从IFT(用于低P123浓度,即1.0和2.0 wt%)和GIFT(用于高于2.0 wt%)分析获得的p(r)函数表明,当摩尔比增加时,混合胶束中的不均匀性增加。这表明C(12)EO(6)在P123胶束的PPO核与PEO冠层之间的界面处自行排列,C(12)烷基链伸展到疏水核中,而EO(6)部分位于亲水冠层中。在P123浓度为5.0 wt%、摩尔比为2.2时,用GIFT获得的结构因子参数显示半径值小于从p(r)函数估计的值。这可以通过一个混合胶束的PEO链渗透到相邻胶束中来解释。在高于转变温度3摄氏度且摩尔比为2.2的条件下,对混合胶束进行了VH-DLS测定。根据分析数据,估计棒的平均长度L为102 nm。