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In situ investigation of adlayer formation and adsorption kinetics of amphiphilic surface-block dendrimers on solid substrates

机译:两亲性表面嵌段树状聚合物在固体基质上的吸附层形成和吸附动力学的原位研究

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The adlayer formation and adsorption kinetics of third- and fourth-generation (G3 and G4) amphiphilic surface-block dendrimers with amino and n-hexyl terminals (amino/hexyl), hydroxyl and n-hexyl terminals (hydroxyl/hexyl), and N-acetyl-D-glucosamine and n-hexyl terminals (glucosamine/hexyl) on solid substrates were investigated using atomic force microscopy, contact angle, surface plasmon resonance spectroscopy, and surface-enhanced infrared absorption spectroscopy. The amino/hexyl and hydroxyl/hexyl dendrimers formed dimer-unit layers on a solid surface, but the whole adlayer of the glucosamine/hexyl dendrimers displayed a rather flat surface, while the adlayer surface of each dendrimer was always hydrophilic. The time dependence of the adlayer formation, which was monitored in situ, obeyed two-step adsorption kinetics, namely, fast and slow adsorption steps. The adsorption amount at the adsorption equilibrium decreased in the order of hydroxyl/hexyl > amino/hexyl > glucosamine/hexyl. dendrimers, and the adsorption amount of the third-generation species was greater than that of the fourth-generation species. The linear dependence of the whole adlayer thickness on the concentration of hydroxyl/hexyl dendrimers was obtained at the equilibrium state. The molecular orientation of the hexyl chains in the adlayers was in the order of amino/hexyl > hydroxyl/hexyl > glucosamine/hexyl dendrimers. [References: 64]
机译:具有氨基和正己基末端(氨基/己基),羟基和正己基末端(羟基/己基)和N的第三代和第四代(G3和G4)两亲性表面嵌段树状聚合物的吸附层形成和吸附动力学使用原子力显微镜,接触角,表面等离振子共振光谱和表面增强红外吸收光谱研究了固体基质上的-乙酰基-D-氨基葡萄糖和正己基末端(氨基葡萄糖/己基)。氨基/己基和羟基/己基树状大分子在固体表面上形成二聚体层,但葡糖胺/己基树状大分子的整个涂层显示出相当平坦的表面,而每个树状大分子的涂层表面总是亲水的。原位监测的吸附层形成的时间依赖性遵循两步吸附动力学,即快速吸附步骤和慢速吸附步骤。吸附平衡时的吸附量按照羟基/己基>氨基/己基>葡糖胺/己基的顺序降低。树枝状大分子,并且第三代物质的吸附量大于第四代物质。在平衡状态下获得了整个外加层厚度对羟基/己基树枝状大分子浓度的线性依赖性。附加层中己基链的分子取向为氨基/己基>羟基/己基>葡糖胺/己基树状大分子的顺序。 [参考:64]

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