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首页> 外文期刊>Macromolecular chemistry and physics >Adhesion of poly(4,4 '-oxydiphenylene pyromellitimide) to copper metal using a polymeric primer: Effects of miscibility and polyimide precursor origin
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Adhesion of poly(4,4 '-oxydiphenylene pyromellitimide) to copper metal using a polymeric primer: Effects of miscibility and polyimide precursor origin

机译:使用聚合物底漆将聚(4,4'-氧二亚苯基均苯四甲酰亚胺)与铜金属粘合:混溶性和聚酰亚胺前体来源的影响

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Poly(amic acid) (PAA) and poly(amic diethyl ester) (PAE) precursors of poly(4,4'-oxydiphenylene pyromellitimide) (PMDA-ODA PI) were synthesized. Miscibility of these precursors with poly(arylene ether benzimidazole) (PAEBI), which is known to exhibit a strong cohesive adhesion to copper metal, was investigated in N-methyl-2-pyrrolidone (NMP) as well as in the condensed and the imidized state. PAEBI is completely miscible with the PAA precursor in NMP and also in the condensed state. This miscibility might result from complex formal of imidazole groups of PAEBI and carboxylic acid groups of precursor. Furthermore, the imidized blend films are optically transparent. However, aggregation of polyimide chains in the films is evident from X-ray diffraction patterns. In contrast, the miscibility of PAEBI and PAE precursor in NMP is limited up to a concentration of 11.06-15.9 wt.-%. They were almost fully immiscible in the condensed state so that phase separation took place during soft-baking. This suggests that there are relatively weak interactions of the imidazole groups of PAEBI with both ester and amide linkages in the precursor, leading to phase separation in the blend. The phase separation occurred further during thermal imidization. The phase separated domains were in a size of greater than or equal to 2.3 mu m, depending on the blend composition. Only the 10/90 and the 90/10 blend films were observed to be optically transparent. The difference in the miscibility of PAEBI with the polyimide precursors is correlated with the adhesion strength of PI/PAEBI/copper joints: higher miscibility results in higher peel strength. [References: 33]
机译:合成了聚(4,4'-氧二亚苯基均苯四甲酰亚胺)(PMDA-ODA PI)的聚(酰胺酸)(PAA)和聚(酰胺二乙酯)(PAE)前体。在N-甲基-2-吡咯烷酮(NMP)以及缩合和酰亚胺化过程中,研究了这些前体与已知对铜金属具有强粘性粘结的聚亚芳基醚苯并咪唑(PAEBI)的混溶性。州。 PAEBI可以与NMP中的PAA前体完全混溶,也可以处于缩合状态。这种混溶性可能是由于PAEBI的咪唑基团与前体的羧酸基团的形式复杂而引起的。此外,酰亚胺化的共混膜是光学透明的。然而,从X射线衍射图可以明显看出膜中聚酰亚胺链的聚集。相反,PAEBI和PAE前体在NMP中的可混溶性受到限制,直至浓度为11.06-15.9 wt .-%。它们在冷凝状态下几乎完全不混溶,因此在软烘烤过程中会发生相分离。这表明前驱体中PAEBI的咪唑基与酯键和酰胺键的相互作用相对较弱,导致共混物中的相分离。在热酰亚胺化期间进一步发生相分离。取决于共混物的组成,相分离的区域的尺寸大于或等于2.3μm。仅观察到10/90和90/10共混物膜是光学透明的。 PAEBI与聚酰亚胺前体的混溶性差异与PI / PAEBI /铜接头的粘合强度有关:较高的混溶性导致较高的剥离强度。 [参考:33]

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