首页> 外文期刊>Journal of Dispersion Science and Technology >Properties of Cationic Polyelectrolyte Layers Adsorbed on Silica and Cellulose Surfaces Studied by QCM-D—Effect of Polyelectrolyte Charge Density and Molecular Weight
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Properties of Cationic Polyelectrolyte Layers Adsorbed on Silica and Cellulose Surfaces Studied by QCM-D—Effect of Polyelectrolyte Charge Density and Molecular Weight

机译:QCM-D研究阳离子吸附在二氧化硅和纤维素表面上的阳离子聚电解质层的性质–聚电解质电荷密度和分子量的影响

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The adsorption of cationic polyelectrolytes (C-PAMs and PDACMAC) with different charge densities and molecular weights on silica and cellulose model surfaces was examined using a quartz crystal microbalance with dissipation, QCM-D. The conformation and viscoelastic properties of the adsorbed polyelectrolyte layers were studied by modelling the data with the Q-Tools program. When comparing the adsorption behavior on cellulose and silica a clear difference both in adsorption kinetics of polyelectrolytes and the viscoelastic properties of the formed polyelectrolyte film was observed. On cellulose the polyelectrolyte films were viscous and more dissipative at the beginning of the adsorption but when the adsorption proceeded the layers became more rigid and stiffer, in contrast to the behavior on silica.
机译:使用带耗散的石英晶体微量天平QCM-D,研究了具有不同电荷密度和分子量的阳离子聚电解质(C-PAM和PDACMAC)在二氧化硅和纤维素模型表面上的吸附。通过使用Q-Tools程序对数据进行建模,研究了吸附的聚电解质层的构象和粘弹性质。当比较在纤维素和二氧化硅上的吸附行为时,观察到聚电解质的吸附动力学和所形成的聚电解质膜的粘弹性质都明显不同。在纤维素上,聚电解质薄膜在吸附开始时是粘性的,并且具有更大的耗散性,但是与二氧化硅上的行为相反,当吸附进行时,各层变得越来越坚硬。

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