Polymer-Surfactant Interactions: Non Ionic Polymers with SDS and DTABr

Camillo La Mesa, Livio Persi, Alessandro D'Aprano
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引用次数: 7

Abstract

Polymer-surfactant interactions in water-SDS-polyvinylpyrrolidone (PVP), water-SDS-polyoxyethylenglycol (PEO), water-(DTABr)-(PEO) and in water-SDS-polyoxypropylenglycol (PPO), systems have been investigated by ultrasonic relaxation, adiabatic compressibility and viscosity measurements.

Both the hydrodynamic and thermodynamic properties show significant changes at the critical association concentration in presence of polymer. As to the kinetic behaviour, investigation on systems containing PEO or PVP indicates the occurrence of a region where relaxation times are nearly constant. For the low molecular weight PPO polymer this effect has not been observed. Such differences have been ascribed to the minimum polymer chain length effect, required for the binding of surfactant aggregates on the polymer backbone. The dynamics of polymer-surfactant interactions has been discussed in terms of a kinetic model, previously proposed.

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聚合物-表面活性剂的相互作用:非离子聚合物与SDS和DTABr
通过超声松弛、绝热压缩率和粘度测量,研究了聚合物-表面活性剂在水- sds -聚乙烯吡罗烷酮(PVP)、水- sds -聚氧乙基乙二醇(PEO)、水-(DTABr)-(PEO)和水- sds -聚氧丙基乙二醇(PPO)体系中的相互作用。在聚合物存在的临界缔合浓度下,水动力和热力学性质都发生了显著变化。在动力学行为方面,对含有PEO或PVP的体系的研究表明,存在一个松弛时间几乎恒定的区域。对于低分子量的PPO聚合物,没有观察到这种效应。这种差异归因于最小的聚合物链长度效应,这是表面活性剂聚集体在聚合物主链上结合所必需的。聚合物-表面活性剂相互作用的动力学已经根据动力学模型进行了讨论。
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