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Comparison of phase structures and surface free energy values for the coatings synthesised from linear polyurethanes and from waterborne polyurethane cationomers

机译:由线性聚氨酯和水性聚氨酯阳离子聚合物合成的涂料的相结构和表面自由能值的比较

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摘要

WAXS, DSC and AFM methods were employed to compare phase structures of the coatings obtained from waterborne polyurethane cationomers which had been synthesised in the reaction of some diisocyanates (MDI, IPDI, TDI and HDI) with polyoxyethylene glycols (M = 600 and 2,000) and butane1,4-diol or N-methyl- or N-butyldiethanolamine and 2,2,3,3-tetrafluoro-1,4-butanediol. The structures were also analysed of the coatings derived from linear polyurethanes which had been synthesised on the basis of similar raw materials. Better rigidity was found for generally amorphous cationomer coats. Changes were discussed in the surface free energy (SFE) values and in their components, as calculated independently with the use of the van Oss–Good and Owens–Wendt methods. Polyurethane coats turned out more hydrophobic as compared to cationomer ones. In both coat types, fluorine incorporated into cationomers contributed to lower SFE values: from 50 down to about 30 mJ/m2.
机译:使用WAXS,DSC和AFM方法比较了由水性聚氨酯阳离子聚合物获得的涂层的相结构,该水性聚氨酯阳离子聚合物是由一些二异氰酸酯(MDI,IPDI,TDI和HDI)与聚氧乙二醇(M = 600和2,000)反应合成的。丁烷1,4-二醇或N-甲基-或N-丁基二乙醇胺和2,2,3,3-四氟-1,4-丁二醇。还分析了由线性聚氨酯衍生的涂层的结构,该线性聚氨酯是在相似原料的基础上合成的。对于一般无定形的阳离子聚合物涂层,发现更好的刚性。讨论了表面自由能(SFE)值及其组成的变化,这些变化是使用van Oss–Good和Owens–Wendt方法独立计算的。与阳离子聚合物相比,聚氨酯涂层的疏水性更高。在两种涂层中,掺入阳离子聚合物中的氟均导致较低的SFE值:从50降至约30 mJ / m 2

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