Ultra-thin films of cationic amphiphilic poly(2-(dimethylamino)ethyl methacrylate) based block copolymers as surface wettability modifiers

被引:17
作者
Nurmi, Leena [1 ]
Holappa, Susanna [2 ]
Nykanen, Antti [3 ]
Laine, Janne [2 ]
Ruokolainen, Janne [3 ]
Seppala, Jukka [1 ]
机构
[1] Aalto Univ, Dept Biotechnol & Chem Technol, FI-02015 Helsinki, Finland
[2] Aalto Univ, Dept Forest Prod Technol, FI-02015 Helsinki, Finland
[3] Aalto Univ, Dept Appl Phys, FI-02015 Helsinki, Finland
关键词
Amphiphilic copolymer; Ultra-thin film; Wettability; TRANSFER RADICAL POLYMERIZATION; SILICA/AQUEOUS SOLUTION INTERFACE; PH-RESPONSIVE BEHAVIOR; 2-(DIMETHYLAMINO)ETHYL METHACRYLATE; POLYELECTROLYTE MULTILAYERS; DIBLOCK COPOLYMERS; AQUEOUS-SOLUTION; MICELLES; MICELLIZATION; ADSORPTION;
D O I
10.1016/j.polymer.2009.08.043
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
Ultra-thin films of cationic amphiphilic block and statistical copolymers were applied on silica surfaces from aqueous solutions through electrostatic interactions, and the resulting modification in the wettability of the surfaces was studied. A copolymer series from 2-(dimethylamino)ethyl methacrylate with methyl methacrylate and butyl methacrylate was polymerized by ATRP. Subsequently, the conformation of the polymers in aqueous solutions was studied by surface tension measurements, dynamic light scattering, H-1 NMR and cryogenic transmission electron microscopy. Unimeric conformation, equilibrium micelles or frozen micellar structures were observed, depending on polymer composition and the ionic strength of the solution. The polymers were applied on silica from aqueous solutions by either spin coating or adsorption. The formed ultra-thin film surfaces were studied by AFM and water contact angle measurements. The spin-coated surfaces were highly hydrophilic with rapidly dropping contact angles, whereas the surfaces prepared by adsorption had stable water contact angles between 30-60 degrees, depending on polymer. The difference between the spin-coated and adsorbed surfaces is explained by the formation of a monolayer in the adsorbed surfaces. (C) 2009 Elsevier Ltd. All rights reserved.
引用
收藏
页码:5250 / 5261
页数:12
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