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疏水改性聚(丙烯酰胺)-共-(丙烯酸)在氨基功能化表面的吸附及其对外部溶剂环境的响应。

Adsorption of hydrophobically modified poly(acrylamide)-co-(acrylic acid) on an amino-functionalized surface and its response to the external solvent environment.

作者信息

Song Xiaoyan, Cao Meiwen, Han Yuchun, Wang Yilin, Kwak Jan C T

机构信息

Key Laboratory of Colloid and Interface Science, Institute of Chemistry, Chinese Academy of Sciences, Beijing 100080, PR China.

出版信息

Langmuir. 2007 Apr 10;23(8):4279-85. doi: 10.1021/la062954u. Epub 2007 Mar 17.

DOI:10.1021/la062954u
PMID:17367169
Abstract

The adsorption of hydrophobically modified poly(acrylamide)-co-(acrylic acid), designated as PAM-C14-AA (x%) (x = 5, 10, 20, representing the mole percent of acrylic acid units), at an amino-functionalized silicon surface was studied. The effect of polymer charge density was determined by varying the acrylic acid content of the copolymer. Characteristics of the adsorbed layer were evaluated by atomic force microscopy, water contact angle measurements, and X-ray photoelectron spectroscopy. The results showed that the adsorption behavior of PAM-C14-AA (x%) is influenced by the balance among the electrostatic, hydrogen-bonding, and hydrophobic interactions. Adjusting the solution pH and polymer charge density significantly affects the morphology and thickness of the adsorbed film. Furthermore, it was found that the adsorbed PAM-C14-AA undergoes conformational rearrangements when the surface is wetted by selected organic solvents. The resultant morphology and wettability of the films indicated that the different affinities of the solvents for different segments of PAM-C14-AA (x%) can be considered to be the possible cause of the conformational rearrangements of adsorbed polymer.

摘要

研究了疏水改性的聚(丙烯酰胺)-共-(丙烯酸),即PAM-C14-AA(x%)(x = 5、10、20,代表丙烯酸单元的摩尔百分比)在氨基功能化硅表面的吸附情况。通过改变共聚物中丙烯酸的含量来确定聚合物电荷密度的影响。通过原子力显微镜、水接触角测量和X射线光电子能谱对吸附层的特性进行了评估。结果表明,PAM-C14-AA(x%)的吸附行为受静电、氢键和疏水相互作用之间平衡的影响。调节溶液pH值和聚合物电荷密度会显著影响吸附膜的形态和厚度。此外,还发现当表面被选定的有机溶剂润湿时,吸附的PAM-C14-AA会发生构象重排。所得薄膜的形态和润湿性表明,溶剂对PAM-C14-AA(x%)不同链段的不同亲和力可被视为吸附聚合物构象重排的可能原因。

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