Material for insulating film, coating varnish for insulating film, and insulating film and semiconductor device using the same
A technology for insulating films and film-forming components, which is used in plastic/resin/wax insulators, semiconductor/solid-state device manufacturing, organic insulators, etc., and can solve the problems of limited decomposable components and no discovery.
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[0080] The present invention will be described in more detail with reference to the following examples. However, the present invention is not limited to these
[0081] Example.
[0082] The specific permittivity, heat resistance, glass transition temperature, and water absorption of the films prepared in Examples and Comparative Examples were measured according to the following methods, and the cross-sections of the films were observed.
[0083] (1) Specific permittivity
[0084] The specific permittivity was measured at a frequency of 100 kHz using an HP-4284A PRECISION LCR METER manufactured by HEWLETT PACKARD in accordance with the method of Japanese Industrial Standard K6911.
[0085] (2) Heat resistance
[0086] The TG / DTA6200 instrument produced by SEIKO INSTRUMENTS Co. Ltd. was used to perform thermogravimetric analysis of the film in a nitrogen flow of 200 ml / min, with a heating rate of 10° C. / min. The temperature at which the weight loss reached 5% was taken as he...
preparation Embodiment 1
[0094] 10 g (96 mmol) of styrene was dissolved in 100 g of tetrahydrofuran dried under a dry nitrogen atmosphere, and the resulting solution was cooled to -78°C. To the cooled solution, 0.77 ml of a 1.3 mol / liter sec-butyllithium solution (solvent: cyclohexane) was added as a reactant for the reaction, and the resulting reaction mixture was stirred for 3 hours. Then, 0.044 g (1.0 mmol) of ethylene oxide was added, and the resulting solution was stirred for 3 hours. After adding 3 g of methanol to the solution, the solution was concentrated to remove the solvent. The resulting product was dissolved in 100 g of tetrahydrofuran and the resulting solution was filtered. The filtrate was vacuum-dried to obtain a styrene oligomer having a hydroxyl group at the chain end and a number average molecular weight of 9600.
[0095] 93 g (9.68 mmol) of the obtained oligomer were dissolved in 80 g of tetrahydrofuran dried under a dry nitrogen atmosphere. To the resulting solution, 1.15 g (...
preparation Embodiment 2
[0097] Except adopting 38.72g (9.68mmol) number-average molecular weight to be 4000 poly(propylene glycol) monobutyl ether [manufactured by ALDRICH company] to replace the 93g (9.68mmol) number-average molecular weight used in Preparation Example 1 to be the styrene oligomer of 9600 Except, all the other were carried out according to the same steps of Preparation Example 1, thereby obtaining a poly(propylene glycol) oligomer having a 4-aminobenzoate group at the chain end and a number average molecular weight of 2500.
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Abstract
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