Poly-butyl glycol fumaric acid ester-based material for environment-friendly LED packaging adhesive and preparation method of poly-butyl glycol fumaric acid ester-based material
A butylene glycol maleate and LED encapsulation technology, which is applied in the direction of adhesives, adhesive additives, non-polymer adhesive additives, etc., can solve the problems of optical properties, mechanical properties, thermal stability, etc., and achieve light transmission The effects of improved performance and heat resistance, short curing time, and high light transmittance
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preparation example Construction
[0024] The final cured product of the LED photosensitive encapsulant made by the preparation process of the present invention is a PBF / PPF-DA cross-linked cured body, i.e. polybutylene fumarate / polypropylene fumarate co-diacrylate cross-linked Joint solidification. By adjusting the light intensity and the distance between the light source and the sample, the curing time of PBF and PPF-DA can be controlled in a short time to meet the curing time requirements of LED photosensitive packaging adhesives. Different ratios of PBF / PPF-DA were prepared, and the physical properties of the cross-linked cured body as LED photosensitive encapsulant were tested. The results show that the cross-linked cured product has higher light transmittance, refractive index, thermal stability and mechanical properties under a certain double bond ratio. The specific instructions are as follows:
[0025] Preparation of component A: Weigh a certain amount of diethyl fumarate, 1,4-butanediol, anhydrous z...
example 1
[0028]Example 1: ① Weigh 1.00g of component A (PBF) and 1.86g of component B (PPF-DA) respectively, and the double bond ratio of component A to component B is 1:2. The weighed components A and B were dissolved in 30 mL of dry dichloromethane and mixed to obtain a mixed solution. ② Stir the mixed solution with a magnetic stirrer and continue stirring for 1 h. After stirring, remove the magnet. The mixed solution was rotary evaporated under vacuum conditions (-0.06MPa), the temperature was set at 37°C, and the rotary evaporation continued for 1h. ③ Seal the mouth of the Erlenmeyer flask containing the mixture after rotary evaporation with coarse filter paper to prevent the volatilization of the mixture, put it in a vacuum drying oven, vacuumize (-0.06MPa) and dry it for 12 hours at room temperature to obtain PBF and Mixture of PPF-DA. ④ Prepare the (2,4,6-trimethylbenzoyl)phenylphosphine oxide (BAPO) solution required for photocrosslinking. BAPO was dissolved in dichlorometh...
example 2
[0030] Example 2: ① Weigh 1.50g of component A (PBF) and 1.40g of component B (PPF-DA) respectively, and the double bond ratio of component A to component B is 1:1. The weighed components A and B were dissolved in 30 mL of dry dichloromethane and mixed to obtain a mixed solution. ② Stir the mixed solution with a magnetic stirrer and continue stirring for 1 h. After stirring, remove the magnet. The mixed solution was rotary evaporated under vacuum conditions (-0.06MPa), the temperature was set at 37°C, and the rotary evaporation continued for 1h. ③ Seal the mouth of the Erlenmeyer flask containing the mixture after rotary evaporation with coarse filter paper to prevent the volatilization of the mixture, put it in a vacuum drying oven, vacuumize (-0.06MPa) and dry it for 12 hours at room temperature to obtain PBF and Mixture of PPF-DA. ④ Prepare the (2,4,6-trimethylbenzoyl)phenylphosphine oxide (BAPO) solution required for photocrosslinking. BAPO was dissolved in dichloromet...
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