Xu Jianquan, Liu Yingjun, He Jinsheng, Zhang Rongping, Zuo Biao, Wang Xinping
Department of Chemistry, Key Laboratory of Advanced Textile Materials and Manufacturing Technology of the Education Ministry, Zhejiang Sci-Tech University, Hangzhou 310018, China.
Soft Matter. 2014 Nov 28;10(44):8992-9002. doi: 10.1039/c4sm01743a.
The effects of the properties of casting solution on the surface structure of poly(methyl methacrylate) (PMMA) films were systematically investigated. It was observed that the hydrophobicity of PMMA films increased with increasing viscosity of the corresponding polymer solution regardless of the film-formation techniques that were utilized. The ratio of the C-H symmetric stretching vibrations of methylene groups (hydrophobic components, with a peak at 2910 cm(-1)) to those of the ester methyl groups (relative hydrophilic components, with a peak at 2955 cm(-1)) from sum frequency generation (SFG) vibrational spectra, A2910/A2955, was used as a parameter to evaluate the structure on the film surface, which was related to the surface wettability of the films. The results showed that A2910/A2955 of cast PMMA films increased linearly with ηsp(0.3) (ηsp, the specific viscosity of the casting solution), whereas that of the corresponding spin-coated films showed a linear relationship defined as ηsp(0.3)E(0.26), where E is the average number of entanglement points per molecule (E = Mw/Me). These results indicate that a relative equilibrium conformation on the PMMA film surface, adopted from the perspective of thermodynamics, was easily achieved during film formation, when the conformation of the polymer chains in the corresponding casting solution was close to that in the bulk. For the spin-coated films, the chain entanglement structure in the casting solution was a more important factor for the resulting film to reach a relative equilibrium state, since this structure was in favor of maintaining the pristine conformation in casting solution under centrifugal force during spin-coating. This work may help to enhance the fundamental understanding of the formation of the film surface structure from polymer solution to the resulting solid film, which will affect not only the corresponding surface properties, but also the dynamics of the resulting thin films.
系统研究了浇铸溶液性质对聚甲基丙烯酸甲酯(PMMA)薄膜表面结构的影响。结果发现,无论采用何种成膜技术,PMMA薄膜的疏水性均随相应聚合物溶液粘度的增加而增大。利用和频振动光谱(SFG)中,亚甲基(疏水成分,峰值在2910 cm⁻¹)的C-H对称伸缩振动与酯甲基(相对亲水成分,峰值在2955 cm⁻¹)的C-H对称伸缩振动的比值A2910/A2955作为评估薄膜表面结构的参数,该参数与薄膜的表面润湿性相关。结果表明,浇铸PMMA薄膜的A2910/A2955随特性粘度ηsp(0.3)(ηsp为浇铸溶液的特性粘度)线性增加,而相应旋涂薄膜的A2910/A2955与ηsp(0.3)E(0.26)呈线性关系,其中E为每个分子的平均缠结点数(E = Mw/Me)。这些结果表明,从热力学角度来看,当相应浇铸溶液中聚合物链的构象与本体中的构象接近时,在成膜过程中很容易在PMMA薄膜表面形成相对平衡的构象。对于旋涂薄膜,浇铸溶液中的链缠结结构是使所得薄膜达到相对平衡状态的更重要因素,因为这种结构有利于在旋涂过程中在离心力作用下保持浇铸溶液中的原始构象。这项工作可能有助于加深对从聚合物溶液到所得固体薄膜的薄膜表面结构形成的基本理解,这不仅会影响相应的表面性质,还会影响所得薄膜的动力学。