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Study of the rheology of aqueous radiation curable polyurethane dispersions modified with associative thickeners

机译:缔合增稠剂改性的水性辐射固化聚氨酯分散体的流变学研究

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The chemistry of radiation curable polyurethane dispersions is outlined with an emphasis on the microstructure of the aqueous polymer dispersion and the possible interactions with associative thickeners. The steady-shear flow was studied for two model dispersions prepared from the same unsaturated polyurethane but showing significantly different particle size distributions. A hydrophobically modified ethoxylated urethane (HEUR) associative thickener with a linear structure was incorporated at different amounts to the dispersions with varying particle volume fractions. The steady-state viscosity at 25 and 10 degrees C was always reached quickly after instant flow rate changes so that no significant thixotropic effects were reported within the experimental timescale. Without thickener, the flow curves of the two model dispersions exhibited a Newtonian behavior except at the highest volume fractions where shear thinning became apparent. The maximum packing values determined from the Krieger-Dougherty relationship were essentially the same for the two systems. In the presence of thickener, the flow curves were characterized by a Newtonian plateau followed by a marked shear thinning region even at low particle volume fractions. This behavior typically suggests the formation of a physical network between polyurethane particles and thickener molecules partly adsorbed onto the polymer surface. The zero-shear viscosity of the two dispersions was compared with respect to: (i) particle volume fraction and (ii) particle surface area at different HEUR concentrations. At a given volume fraction, the particle size affects the viscosity of thickened models. As a corollary, a relationship is found between the particles size and the level of thickener required to reach a target viscosity. This study offers practically relevant data in terms of application conditions and provides a better insight into the thickening protocol. (C) 2008 Elsevier B.V. All rights reserved.
机译:概述了可辐射固化聚氨酯分散体的化学过程,重点是水性聚合物分散体的微观结构以及与缔合性增稠剂的可能相互作用。研究了由相同的不饱和聚氨酯制备的两种模型分散体的稳态剪切流,但显示出明显不同的粒径分布。将具有线性结构的疏水改性乙氧基化氨基甲酸酯(HEUR)缔合型增稠剂以不同的量掺入具有不同颗粒体积分数的分散体中。瞬时流量变化后,总是很快达到25和10摄氏度的稳态粘度,因此在实验时间内没有明显的触变效应报道。在没有增稠剂的情况下,两种模型分散体的流动曲线都表现出牛顿行为,除了在最高体积分数下剪切变稀变得明显。由克里格-多尔蒂关系确定的最大装箱值对于两个系统基本上是相同的。在存在增稠剂的情况下,即使在低颗粒体积分数下,流动曲线的特征也在于牛顿平台,其后是明显的剪切稀化区域。这种行为通常表明在聚氨酯颗粒和部分吸附到聚合物表面的增稠剂分子之间形成了物理网络。比较两种分散体的零剪切粘度:(i)颗粒体积分数和(ii)在不同HEUR浓度下的颗粒表面积。在给定的体积分数下,粒径会影响增稠模型的粘度。作为推论,在粒径与达到目标粘度所需的增稠剂含量之间存在关系。这项研究提供了有关应用条件的实用数据,并提供了对增稠方案的更好了解。 (C)2008 Elsevier B.V.保留所有权利。

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