Forces between polymer surfaces and self-assembled monolayers

被引:15
作者
Singh, Jagdeep
Whitten, James E. [1 ]
机构
[1] Univ Massachusetts Lowell, Dept Chem, Lowell, MA 01854 USA
来源
JOURNAL OF MACROMOLECULAR SCIENCE PART A-PURE AND APPLIED CHEMISTRY | 2008年 / 45卷 / 11期
基金
美国国家科学基金会;
关键词
force spectroscopy; poly(acrylic acid); polystyrene; self-assembled monolayers; surface free energy; photoelectron spectroscopy;
D O I
10.1080/10601320802378186
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
Gold-coated atomic force microscope (AFM) tips functionalized with amine-, hydroxyl-, carboxylic acid-, and methyl-terminated alkanethiol molecules were used to probe the adhesive forces of polystyrene and poly(acrylic acid) films in dry air (relative humidity < 0.5%). X-ray photoelectron spectroscopy (XPS) and contact angle measurements confirmed the quality and uniformity of similarly treated gold surfaces and the polymer films. XPS indicated that the amine-functionalized thiol films were protonated and comprised of multilayers. Contact angle data were used to calculate surface free energies, and DMT theory yielded the works of adhesion and interfacial free energies for the tip-substrate combinations. In the case of polystyrene, the work of adhesion followed the order methyl > carboxylic acid > hydroxyl > amine. For poly(acrylic acid), the observed order was hydroxyl > amine > carboxylic acid > methyl.
引用
收藏
页码:884 / 891
页数:8
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