Department of Chemistry, Technical University of Denmark, 2800 Kgs. Lyngby, Denmark.
Department of Chemistry, University of Oslo, Blindern, P.O. Box 1033, Blindern, N-0315 Oslo, Norway, Norway.
J Colloid Interface Sci. 2017 Nov 1;505:546-555. doi: 10.1016/j.jcis.2017.06.044. Epub 2017 Jun 15.
The properties of synthesized diblock poly(N-isopropylacrylamide)-poly((3-acrylamidopropyl)trimethylammonium chloride) and triblock methoxy-poly(ethylene glycol)-poly(N-isopropylacrylamide)-poly((3-acrylamidopropyl)trimethylammonium chloride) cationic copolymers at the silica/aqueous interface are investigated using quartz crystal microbalance with dissipation monitoring (QCM-D) and atomic force microscopy (AFM). Moreover, dynamic light scattering is employed to assess the copolymers in terms of the hydrodynamic size and interchain aggregation. Although viscoelastic Voigt modeling of the QCM-D data suggests a comparable layer thickness for the copolymers on the silica surface, the AFM imaging and colloidal probe measurements reveal significant differences in surface coverage and thickness of the layers, which are discussed and compared with respect to the stabilization effect by the hydrophilic poly(ethylene glycol) block.
采用石英晶体微天平(QCM-D)和原子力显微镜(AFM)研究了合成的二嵌段聚(N-异丙基丙烯酰胺)-聚((3-丙烯酰胺丙基)三甲基氯化铵)和三嵌段甲氧基聚(乙二醇)-聚(N-异丙基丙烯酰胺)-聚((3-丙烯酰胺丙基)三甲基氯化铵)阳离子共聚物在二氧化硅/水界面的性质。此外,还采用动态光散射评估了共聚物的水动力尺寸和链间聚集。尽管 QCM-D 数据的粘弹性 Voigt 模型表明共聚物在二氧化硅表面的层厚度相当,但 AFM 成像和胶体探针测量揭示了表面覆盖和层厚度的显著差异,这些差异将根据亲水的聚(乙二醇)块的稳定作用进行讨论和比较。