Fuensanta Mónica, Khoshnood Abbas, Martín-Martínez José Miguel
Adhesion and Adhesives Laboratory, University of Alicante, 03080 Alicante, Spain.
Polymers (Basel). 2020 Oct 26;12(11):2478. doi: 10.3390/polym12112478.
Dimethylolpropionic acid (DMPA) internal emulsifier has been added before, during and after prepolymer formation in the synthesis of waterborne poly(urethane-urea)s (PUDs) and their structure-properties relationships have been assessed. PUDs were characterized by pH, viscosity and particle size measurements, and the structure of the poly(urethane-urea) (PU) films was assessed by infra-red spectroscopy, differential scanning calorimetry, X-ray diffraction, thermal gravimetric analysis, plate-plate rheology and dynamic mechanical thermal analysis. The adhesion properties of the PUDs were measured by cross-hatch adhesion and T-peel test. The lowest pH value and the highest mean particle size were found in the PUD made by adding DMPA prepolymer formation, all PUDs showed relatively ample mono-modal particle size distributions. The highest viscosity and noticeable shear thinning were obtained in the PUD made by adding DMPA prepolymer formation. Depending on the stage of addition of DMPA, the length of the prepolymer varied and the PU films showed different degree of micro-phase separation. Because the shortest prepolymer was formed in the PU made with DMPA added prepolymer, this PU film showed the lowest storage moduli and early melting indicating higher degree of micro-phase separation. The highest storage modulus, later melting, higher temperature and lower modulus at the cross between the storage and loss moduli corresponded to the PU made by adding DMPA prepolymer formation, because the longer prepolymer produced during synthesis. The lowest thermal stability corresponded to the PU made by adding DMPA prepolymer formation and the structures of all PU films were dominated by the soft domains, the main structural differences derived from the hard domains. Whereas DMPA-isophorone diisocyanate (IPDI) urethane and urea hard domains were created in the PU film made by adding DMPA prepolymer formation, the other PU films showed DMPA-IPDI, polyester-IPDI and two different DMPA-IPDI-polyester hard domains. Finally, the adhesion properties of the PUDs and PU coatings were excellent and they were not influenced by the structural differences caused by adding DMPA in different stages of the synthesis.
在水性聚(聚氨酯 - 脲)(PUDs)的合成过程中,已在预聚物形成之前、期间和之后添加了二羟甲基丙酸(DMPA)内乳化剂,并评估了它们的结构 - 性能关系。通过pH值、粘度和粒径测量对PUDs进行了表征,并通过红外光谱、差示扫描量热法、X射线衍射、热重分析、平板流变学和动态热机械分析对聚(聚氨酯 - 脲)(PU)薄膜的结构进行了评估。通过划格附着力和T型剥离试验测量了PUDs的附着力性能。在预聚物形成过程中添加DMPA制备的PUD中发现了最低的pH值和最高的平均粒径,所有PUDs均显示出相对充足的单峰粒径分布。在预聚物形成过程中添加DMPA制备的PUD中获得了最高的粘度和明显的剪切变稀现象。根据DMPA的添加阶段,预聚物的长度会发生变化,并且PU薄膜表现出不同程度的微相分离。由于在添加DMPA的预聚物制备的PU中形成的预聚物最短,该PU薄膜显示出最低的储能模量和早期熔化,表明微相分离程度更高。最高的储能模量、较晚的熔化、储能模量和损耗模量交叉处的较高温度和较低模量对应于在预聚物形成过程中添加DMPA制备的PU,因为在合成过程中产生的预聚物较长。最低的热稳定性对应于在预聚物形成过程中添加DMPA制备的PU,并且所有PU薄膜的结构均以软段为主,主要结构差异源自硬段。在预聚物形成过程中添加DMPA制备的PU薄膜中形成了DMPA - 异佛尔酮二异氰酸酯(IPDI)聚氨酯和脲硬段,而其他PU薄膜则显示出DMPA - IPDI、聚酯 - IPDI和两种不同的DMPA - IPDI - 聚酯硬段。最后,PUDs和PU涂层的附着力性能优异,并且不受合成不同阶段添加DMPA所引起的结构差异的影响。