Sustainable associative thickeners based on hydrophobically modified ethoxylated poly(hydroxy-urethane)s end-capped by long alkyl chains

材料科学 异氰酸酯 聚氨酯 聚合物 流变学 高分子化学 预聚物 烷基 水溶液 碳酸乙烯酯 化学工程 共聚物 溶剂 摩尔质量 乙二醇 环氧乙烷 有机化学 化学 复合材料 电极 物理化学 工程类 电解质
作者
Dominik Wołosz,Aleksandra Marta Fage,Paweł G. Parzuchowski,Aleksandra Świderska,Robert Brüll,Peter Elsner
出处
期刊:Progress in Organic Coatings [Elsevier]
卷期号:179: 107514-107514 被引量:6
标识
DOI:10.1016/j.porgcoat.2023.107514
摘要

Hydrophobically modified ethoxylated urethanes (HEURs) are associative polymers applied as thickening additives in various waterborne systems, such as emulsions, coatings and printing inks. Their conventional synthesis, based on diisocyanates, poses environmental and health threats during both manufacture and application. Hence, in this paper we present an approach for the next generation of sustainable and CO2-rich polyurethane rheological modifiers – isocyanate-free HEURs (IFHEURs) obtained through poly(hydroxy-urethane) route. The hydrophilic core of the IFHEURs was prepared by step-growth polyaddition between diamine and poly(ethylene glycol) bis(cyclic carbonate) – synthesized using CO2 as a green source of the carbonate bonds. Such obtained prepolymer with terminal carbonate groups was subsequently modified with hydrophobic amines using reactive extrusion method, which enabled efficient homogenisation of the viscous reaction systems and reaching high end-capping functionality after only 2 h. In contrast to previously reported studies, the synthetic procedure was both solvent- and catalyst-free and allowed to incorporate up to 11 wt% of CO2 into the backbone of the final products. The structural analysis of the obtained IFHEURs using NMR and FT-IR spectroscopy and MALDI-ToF mass spectrometry confirmed obtaining the desired telechelic architecture resembling standard HEUR materials. The associative behavior of the IFHEURs in aqueous solutions was addressed in a rheological study, which revealed typical thickening mechanisms exhibited by rheological additives.
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