Oxazolidone ring-containing epoxy resin, method for producing the thereof, epoxy resin composition, cured product and application thereof
An oxazolidone ring, epoxy resin technology, applied in the application, other household appliances, chemical instruments and methods, etc., can solve the deterioration of adhesion, insufficient adhesion, deterioration of dielectric constant phosphorus content, etc. problems, to achieve the effects of excellent dielectric properties, good flame retardancy, and low dielectric constant
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[0227] Hereinafter, 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 measuring method can be measured according to the following methods, respectively. The unit of equivalent is g / eq.
[0228] ・Epoxy equivalent: According to JIS K7236 standard.
[0229] · Viscosity: According to JIS K7233 standard, single cylinder rotational viscometer method.
[0230] · Softening point: Measured according to the JIS K7234 standard and the ring and ball method. Specifically, an automatic softening point device (manufactured by Mindac Co., Ltd., ASP-MG4) was used.
[0231] ·Solvent solubility: The state when it diluted with methyl ethyl ketone to 50% of non-volatile content was judged visually. The case of being completely dissolved and transparent was rated as "◯", the case of cloudy or separat...
Synthetic example 1
[0243] 100 parts of 4,4'-(3,3,5-trimethylcyclohexylene)diphenol (BisP-TMC), 358 parts of epichlorohydrin, 4 parts of Ion-exchanged water was heated up to 50°C while stirring. After uniform dissolution, 5.3 parts of 49% sodium hydroxide aqueous solution was charged and reacted for 3 hours. Next, after raising the temperature to 64°C, reduce the pressure to such an extent that reflux of water occurs, and add 48 parts of 49% sodium hydroxide aqueous solution dropwise over 3 hours. Alcohol, epichlorohydrin was returned to the reaction vessel, and water was removed from the system to perform the reaction. After completion of the reaction, the temperature was increased to 70° C. to perform dehydration, and the temperature was set to 135° C. to collect remaining epichlorohydrin. It returned to normal pressure, and 204 parts of methyl isobutyl ketones (MIBK) were added and dissolved. 127 parts of ion-exchanged water was added, stirred and left still to dissolve and remove the commo...
Synthetic example 2
[0245] Except having changed epichlorohydrin into 179 parts, the same operation was performed using the apparatus similar to the synthesis example 1, and the epoxy resin (a-2) represented by the said formula (7) was obtained. The epoxy equivalent of the obtained epoxy resin (a-2) was 227, the alcoholic hydroxyl equivalent was 3800, and m was 0.09.
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