首页> 外文期刊>Journal of Polymer Science, Part B. Polymer Physics >Structure and rheology of hyperbranched and dendritic polymers. II. Effects of blending acetylated and hydroxy-terminated poly(propyleneimine) dendrimers with aqueous poly(ethylene oxide) solutions
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Structure and rheology of hyperbranched and dendritic polymers. II. Effects of blending acetylated and hydroxy-terminated poly(propyleneimine) dendrimers with aqueous poly(ethylene oxide) solutions

机译:超支化和树枝状聚合物的结构和流变学。二。乙酰化和羟基封端的聚亚丙基亚胺树枝状聚合物与聚环氧乙烷水溶液共混的影响

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The effect of adding acetylated poly(propyleneimine) dendrimers to the structure and rheology of aqueous solutions of high molecular weight poly(ethylene oxide) (PEO) was investigated by rheology and small-angle neutron scattering in a temperature range of 10-40 degrees C. In the semidilute regime, the steady shear rheology of PEO solutions was unmodified by the addition of dendrimers at a comparable weight concentration. At the highest concentrations studied, the addition of acetylated dendrimers suppressed the onset of a low-frequency elastic modulus at the lowest temperature investigated. For comparison, the addition of PEO of a comparable molecular weight at the same weight fr action resulted in a milder suppression but, unlike the dendrimers, greatly increased the solution viscosity. The addition of acetylated dendrimers to a semidilute PEO solution at 10 degrees C substantially reduced the solution turbidity. These effects on the rheology and optical properties were confirmed by small-angle neutron scattering measurements of the molecular structure of the mixture. Additional SANS measurements in the dilute regime (0.1 wt % PEG) showed quantitatively that the dendrimers decorated the PEO chains in a necklace structure, such as that observed previously for micelles. The results suggested a mechanism of rheology modification whereby the dendrimers disrupted the association network structure in the PEO solution at lower temperatures by preferentially associating with the PEO chains in solution. (C) 2000 John Wiley & Sons. Inc. [References: 19]
机译:通过流变学和小角度中子散射在10-40摄氏度的温度范围内研究了向高分子量聚环氧乙烷(PEO)水溶液的结构和流变性中添加乙酰化聚亚丙基亚胺树状大分子的影响。在半稀释状态下,PEO溶液的稳定剪切流变性没有通过在可比较的重量浓度下添加树枝状聚合物来改变。在所研究的最高浓度下,乙酰化树状聚合物的加入抑制了所研究的最低温度下低频弹性模量的产生。为了进行比较,以相同的重量fr作用加入具有可比分子量的PEO导致抑制作用较温和,但与树枝状聚合物不同,它大大提高了溶液粘度。在10摄氏度将乙酰化树状大分子添加到半稀释的PEO溶液中,可以大大降低溶液的浊度。通过对混合物分子结构的小角度中子散射测量证实了这些对流变学和光学性质的影响。稀溶液(0.1 wt%PEG)中的其他SANS测量定量显示,树枝状聚合物修饰了项链结构中的PEO链,例如以前观察到的胶束。结果提示了一种流变改性的机制,其中树枝状聚合物通过优先与溶液中的PEO链缔合,从而在较低温度下破坏了PEO溶液中的缔合网络结构。 (C)2000 John Wiley&Sons。 Inc. [参考:19]

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