Polyimide with high bonding strength as well as preparation method and application thereof
A polyimide, bonding strength technology, applied in the direction of adhesives, circuits, electrical solid devices, etc., can solve the problem of increasing the dielectric constant and dielectric loss tangent, hindering high-frequency transportation, increasing polyimide and copper Adhesive strength and other issues to achieve the effect of improving other properties, high selectivity, and enhancing adhesive strength
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[0039]Wherein, described preparation method (1) comprises the following steps:
[0040] Step S11, synthesizing polyamic acid: dissolving diamine in a polar organic solvent and then adding dianhydride to synthesize a first polyamic acid solution.
[0041] Step S12, grafting polyamic acid: adding a grafting compound to the first polyamic acid solution to carry out a grafting reaction to obtain a second polyamic acid solution.
[0042] Step S13, imidization reaction: thermal imidization of the second polyamic acid solution to obtain a polyimide with high adhesive strength.
[0043] Wherein, described preparation method (two) comprises the following steps:
[0044] Step S21 , synthesizing polyamic acid: dissolving diamine in a polar organic solvent and then adding dianhydride to synthesize a first polyamic acid solution.
[0045] Step S22, imidization reaction: adding an imidization agent and an imidization accelerator to the first polyamic acid solution for chemical imidization...
Embodiment 1
[0090] S11. Synthetic polyamic acid
[0091] 2-(4-Aminophenyl)-5-aminobenzimidazole and 2,2-bis(3-amino-4-hydroxyphenyl)hexafluoropropane were placed in a vacuum oven at 60°C for 3h, and the homophenylene The tetracarboxylic dianhydride was treated in a vacuum oven at 160 °C for 4 h to remove impurities.
[0092] At room temperature, 1.6019g of 2-(4-aminophenyl)-5-aminobenzimidazole and 1.1212g of 2,2-bis(3-amino-4-hydroxyphenyl)hexafluoropropane were dissolved in 28.1089g of N, N-dimethylacetamide, and then under a nitrogen atmosphere, 2.2373 g of pyromellitic dianhydride was added twice while stirring and stirred for 24 h to synthesize the first polyamic acid solution.
[0093] S12, grafted polyamic acid
[0094] To the first polyamic acid solution, add 4-epoxypropaneoxy carbazole with the same molar amount of hydroxyl to carry out the grafting reaction, and after the reaction is finished, add acetonitrile to wash out the grafted polymer with the structure of chemical inte...
Embodiment 2
[0099] Compared with Example 1, the difference between Example 2 and Example 1 is that the diamine monomers used in this example are 2-(4-aminophenyl)-5-aminobenzimidazole and 2,2,0,0,0 having a molar ratio of 1:1. 2-Bis(3-amino-4-hydroxyphenyl)hexafluoropropane. The rest of the materials and the preparation process in this example are exactly the same as those in Example 1, so they will not be repeated.
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