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原子力显微镜和超声力显微镜对由两种不相容聚合物——聚苯乙烯和聚甲基丙烯酸丁酯形成的吸附层的研究。

Atomic force and ultrasonic force microscopy investigation of adsorbed layers formed by two incompatible polymers: polystyrene and poly(butyl methacrylate).

作者信息

Bliznyuk V N, Lipatov Y S, Ozdemir N, Todosijchuk T T, Chornaya V N, Singamaneni S

机构信息

College of Engineering and Applied Sciences, Western Michigan University, Kalamazoo, Michigan 49008, USA.

出版信息

Langmuir. 2007 Dec 18;23(26):12973-83. doi: 10.1021/la701644n. Epub 2007 Nov 10.

Abstract

Atomic force microscopy (AFM) and ultrasonic force microscopy (UFM) have been used to study the properties of adsorption layers formed by two incompatible polymers, polystyrene and poly(butyl methacrylate), in the course of simultaneous adsorption on the surface of silica (naturally oxidized surface of a silicon wafer). The adsorption was performed from solutions containing both of the components in a common solvent (carbon tetrachloride) in dilute and semidilute concentration regimes. It was discovered that in both cases the structure of adsorption layers has a complex mosaic structure, the details of which depend on solution composition, on the solution concentration regime, and on the ratio of the components in the adsorption layer. The observed structural inhomogeneity on the length scale of approximately 200-500 nm (distribution of segment density revealed by UFM) appears as result of thermodynamic incompatibility in the system and is conditioned by changes in the conformation states of the adsorbed macromolecules in the route of competitive adsorption of the components. The adsorbed polymer films with thicknesses of approximately 20-500 nm appeared to have fractal properties and could be characterized with fractal dimensions dependent on the ratio of the components at the interface and the adsorption conditions.

摘要

原子力显微镜(AFM)和超声力显微镜(UFM)已被用于研究由两种不相容聚合物——聚苯乙烯和聚甲基丙烯酸丁酯,在同时吸附于二氧化硅(硅片的自然氧化表面)表面过程中形成的吸附层的性质。吸附是在稀溶液和半稀溶液浓度范围内,从含有两种组分的共溶剂(四氯化碳)溶液中进行的。结果发现,在这两种情况下,吸附层的结构都具有复杂的镶嵌结构,其细节取决于溶液组成、溶液浓度范围以及吸附层中各组分的比例。在大约200 - 500 nm长度尺度上观察到的结构不均匀性(由UFM揭示的链段密度分布)是系统中热力学不相容的结果,并且是由各组分竞争吸附过程中吸附大分子构象状态的变化所决定的。厚度约为20 - 500 nm的吸附聚合物膜表现出分形特性,并且可以用取决于界面处各组分比例和吸附条件的分形维数来表征。

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