Construction of wettability gradient surface on copper substrate by controlled hydrolysis of poly(methyl methacrylate-butyl acrylate) films

被引:10
|
作者
Zhang, Yong [1 ]
Cheng, Jiang [2 ]
Yang, Zhuo-ru [2 ]
机构
[1] Guangzhou Panyu Polytech, Guangzhou 511483, Guangdong, Peoples R China
[2] S China Univ Technol, Sch Chem & Chem Engn, Guangzhou 510640, Guangdong, Peoples R China
基金
中国国家自然科学基金;
关键词
Methyl methacrylate; Butyl acrylate; Polymerization; Gradient wetting; Hydrolysis; STIMULATED DEPOLARIZATION CURRENT; P(MMA/BA) COPOLYMERS; PROTEIN ADSORPTION; POLYETHYLENE; STREPTAVIDIN; RESPONSES; ADHESION; BIOTIN; PLASMA;
D O I
10.1016/j.apsusc.2014.07.045
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
We report a gradient wettability surface on copper slide prepared by a simple controlled ester group hydrolysis procedure of poly(methyl methacrylate-butyl acrylate) [P (MMA-BA)] films coated on the copper substrate. In the method, sodium hydroxide solutions are selected to prepare surface gradient wettability on P (MMA-BA) films. The P (MMA-BA) copolymers with different MMA contents are first synthesized by a conventional free atom radical solution polymerization method. The transfer of surface chemical composition from the ester group to acid salt is achieved by hydrolysis in NaOH solution. The effects of different concentrations of NaOH solution and reaction times on the physicochemical properties of the resulting surfaces are studied. The field-emission scanning electron microscopy (FESEM), atomic force microscopy (AFM) and X-ray photoelectron spectroscopy (XPS) results show that the varying concentration along the substrate length is only attributed to the hydrolysis reaction of ester groups. The hydrolysis causes insignificant change on the morphology of the original film on the copper substrate. In addition, it is found that the MMA copolymer content has a significant influence on the concentration of ester groups on the outermost surface and thus important for forming the slope gradients. (C) 2014 Elsevier B.V. All rights reserved.
引用
收藏
页码:163 / 168
页数:6
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