Sugimoto Yuka, Nishimura Yukihiro, Uehara Fai, Matsumoto Akikazu
Department of Applied Chemistry, Graduate School of Engineering, Osaka Prefecture University, 1-1 Gakuen-cho, Naka-ku, Sakai, Osaka 599-8531, Japan.
ACS Omega. 2018 Jul 9;3(7):7532-7541. doi: 10.1021/acsomega.8b00920. eCollection 2018 Jul 31.
The epoxy monolith with a highly porous structure is fabricated by the thermal curing of 2,2-bis(4-glycidyloxyphenyl)propane and 4,4'-methylenebis(cyclohexylamine) in the presence of poly(ethylene glycol) as the porogen via polymerization-induced phase separation. In this study, we demonstrated a new type of dissimilar material bonding method for various polymers and metals coated with the epoxy monolith. On the basis of scanning electron microscopy (SEM) observations, the pore size and number of epoxy monoliths were evaluated to be 1.1-114 μm and 8.7-48 200 mm, respectively, depending on the ratio of the epoxy resin and cross-linking agent used for the monolith fabrication. Various kinds of thermoplastics, such as polyethylene, polypropylene, polyoxymethylene, acrylonitrile-butadiene-styrene copolymer, polycarbonate bisphenol-A, and poly(ethylene terephthalate), were bonded to the monolith-modified metal plates by thermal welding. The bond strength for the single lap-shear tensile test of stainless steel and copper plates with the thermoplastics was in the range of 1.2-7.5 MPa, which was greater than the bond strength value for each bonding system without monolith modification. The SEM observation of fractured test pieces directly confirmed an anchor effect on this bonding system. The elongated deformation of the plastics that filled in the pores of the epoxy monolith, was observed. It was concluded that the bond strength significantly depended on the intrinsic strength of the used thermoplastics. The epoxy monolith bonding of hard plastics, such as polystyrene and poly(methyl methacrylate), was performed by the additional use of adhesives, solvents, and a reactive monomer. The epoxy monolith sheets were also successfully fabricated and applied to dissimilar material bonding.
通过在作为致孔剂的聚乙二醇存在下,使2,2-双(4-缩水甘油氧基苯基)丙烷和4,4'-亚甲基双(环己胺)进行热固化,经由聚合诱导相分离制备出具有高度多孔结构的环氧整体材料。在本研究中,我们展示了一种用于各种涂覆有环氧整体材料的聚合物和金属的新型异种材料粘结方法。基于扫描电子显微镜(SEM)观察,根据用于整体材料制备的环氧树脂和交联剂的比例,环氧整体材料的孔径和孔数分别评估为1.1 - 114μm和8.7 - 48200个/mm。通过热焊接将各种热塑性塑料,如聚乙烯、聚丙烯、聚甲醛、丙烯腈-丁二烯-苯乙烯共聚物、聚碳酸酯双酚A和聚对苯二甲酸乙二酯,粘结到整体材料改性的金属板上。不锈钢和铜板与热塑性塑料的单搭接剪切拉伸试验的粘结强度在1.2 - 7.5MPa范围内,这大于未进行整体材料改性的每个粘结体系的粘结强度值。对断裂试件的SEM观察直接证实了该粘结体系存在锚固效应。观察到填充在环氧整体材料孔隙中的塑料发生了伸长变形。得出的结论是,粘结强度显著取决于所用热塑性塑料的固有强度。通过额外使用粘合剂、溶剂和反应性单体,实现了聚苯乙烯和聚甲基丙烯酸甲酯等硬塑料的环氧整体材料粘结。还成功制备了环氧整体材料片材并将其应用于异种材料粘结。