FLAME RETARDANT EPOXY RESIN COMPOSITION,prepreg product, insulation sheet, adheresion sheet, laminated plate, sealing material, casting material and solidifying material
A technology of epoxy resin and flame retardancy, which is applied in the field of epoxy resin cured products, can solve problems such as deterioration of adhesion, and achieve the effects of low dielectric constant, excellent dielectric properties, and excellent properties
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[0178] Although an Example and a comparative example are given and this invention is demonstrated concretely, this invention is not limited to these examples. Unless otherwise specified, "part" means a mass part, and "%" means a mass %. In addition, the measurement method can perform measurement according to the following methods, respectively.
[0179] Epoxy equivalent: According to JIS K7236 standard.
[0180] Softening point: Measured according to JIS K7234 standard and ring and ball method. Specifically, an automatic softening point device (manufactured by Mindac Co., Ltd., ASP-MG4) was used.
[0181] Oxazolidone ring content (Ox, eq. / kg): In the oxazolidone ring formation reaction in this example, the epoxy group is not substantially used except for the oxazolidone ring formation reaction, so it can be It can be calculated|required from the following formula.
[0182] Ox=((Wt0 / Ep0)-(Wt / Ep)) / Wt×1000
[0183] Here, Ep0 is the epoxy equivalent (g / eq.) of the raw materia...
Synthetic example 1
[0192] Synthesis Example 1a
[0193] 2,500 parts of phenol and 7.5 parts of oxalic acid dihydrate were placed in a separable glass flask equipped with a stirring device, a thermometer, a nitrogen gas introduction device, a condenser pipe, and a dropping device, and stirred while injecting nitrogen gas, and heated. heat up. Next, 474.1 parts of 37.4% formalin was dripped and made to react over 30 minutes, stirring at 80 degreeC. Further, reaction was performed for 3 hours while maintaining the reaction temperature at 92°C. The temperature was raised, and the reaction product water was removed to the outside of the system, and the temperature was raised to 110°C. Residual phenol was recovered at 160° C. under reduced pressure, and the temperature was further increased to 250° C. to recover a part of dinuclear bodies to obtain a phenol novolak resin (1a) in which dinuclear bodies were reduced. The dinuclear body content rate and trinuclear body content rate of the obtained phe...
Synthetic example 2
[0200] Change diphenylmethane diisocyanate into polymethylene polyphenyl polyisocyanate (manufactured by Mitsui Chemicals Co., Ltd., Cosmonet M-50, NCO concentration is 34%) 7.5 parts (equivalent ratio (e / d ) = 0.10), and synthesized using the same apparatus and procedure as in Synthesis Example 1c to obtain an oxazolidone ring-containing novolak-type epoxy resin (resin 2).
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