Phenolic resin, epoxy resin, epoxy resin comosition and cured product of same
A technology of epoxy resin and phenolic resin, which is applied in the field of printed wiring board, laminated board, prepreg, epoxy resin hardened product, and epoxy resin composition, and can solve the problem of undisclosed multiple dicyclopentadiene substitution , Insufficient epoxy resin, poor adhesion and other problems, to achieve excellent dielectric loss tangent, copper foil peel strength and excellent interlayer adhesion strength
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Embodiment 1
[0145] 970 parts of 2,6-xylenol and 47% BF 3 14.5 parts of ether complexes were heated to 70°C while stirring. While maintaining the same temperature, 300 parts of dicyclopentadiene (0.29 times mole relative to 2,6-xylenol) was added dropwise over 2 hours. Furthermore, it reacted at the temperature of 125 degreeC - 135 degreeC for 6 hours, and added 2.3 parts of calcium hydroxide. Furthermore, 4.6 parts of 10% aqueous oxalic acid solutions were added. Then, after heating to 160 degreeC and dehydrating, it heated to 200 degreeC under the reduced pressure of 5 mmHg, and evaporated and removed the unreacted raw material. 1000 parts of methyl isobutyl ketone (MIBK) was added to dissolve the product, 400 parts of warm water at 80° C. was added to perform water washing, and the lower water tank was separated and removed. Then, under a reduced pressure of 5 mmHg, it was heated to 160° C., MIBK was evaporated and removed, and 540 parts of reddish-brown phenol resin (A1) were obtain...
Embodiment 2
[0147] Into the same reaction device as in Example 1, 832 parts of 2,6-xylenol, 47% BF were charged 3 12.4 parts of ether complexes were heated to 70°C while stirring. While maintaining the same temperature, 300 parts of dicyclopentadiene (0.33 times mole relative to 2,6-xylenol) was added dropwise over 2 hours. Furthermore, it reacted at the temperature of 125 degreeC - 135 degreeC for 6 hours, and added 2.0 parts of calcium hydroxide. Furthermore, 4.0 parts of 10% aqueous oxalic acid solutions were added. Then, after heating to 160 degreeC and dehydrating, it heated to 200 degreeC under the reduced pressure of 5 mmHg, and evaporated and removed the unreacted raw material. 1000 parts of MIBK was added to dissolve the product, 400 parts of warm water at 80° C. was added to perform water washing, and the lower water tank was separated and removed. Then, under a reduced pressure of 5 mmHg, it was heated to 160° C., MIBK was evaporated and removed, and 540 parts of reddish-bro...
Embodiment 3
[0149] Into the same reaction device as in Example 1, 693 parts of 2,6-xylenol, 47% BF 3 10.4 parts of ether complexes were heated to 70°C while stirring. While maintaining the same temperature, 300 parts of dicyclopentadiene (0.40 times mole relative to 2,6-xylenol) was added dropwise over 2 hours. Furthermore, it reacted at the temperature of 125 degreeC - 135 degreeC for 6 hours, and added 1.7 parts of calcium hydroxide. Furthermore, 3.3 parts of 10% aqueous oxalic acid solutions were added. Then, after heating to 160 degreeC and dehydrating, it heated to 200 degreeC under the reduced pressure of 5 mmHg, and evaporated and removed the unreacted raw material. 1800 parts of MIBK was added to dissolve the product, 650 parts of warm water at 80° C. was added to perform water washing, and the lower water tank was separated and removed. Then, MIBK was heated to 160 degreeC under the reduced pressure of 5 mmHg, and MIBK was evaporated, and 1040 parts of reddish-brown phenol res...
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