A kind of preparation method of silicone resin
The technology of silicone resin and phenyl trialkoxy silane is applied in the field of preparation of high molecular weight vinyl phenyl silicone resin for LED encapsulation reinforcement, which can solve the problem that the preparation method of polysilsesquioxane is not included, and the packaging materials are affected. Light transmittance, poor mechanical properties of vulcanizates, etc., to achieve the effect of improving mechanical properties, large spatial dimensions, and excellent thermal stability.
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Examples
Embodiment 1
[0047] Add 40 parts of phenyltriethoxysilane, 100 parts of xylene, and 400 parts of deionized water into a 500ml dry four-neck flask, stir rapidly at 40°C under a nitrogen atmosphere, perform a hydrolysis reaction for 1.5 hours, and heat up to 80 ℃, add 5 parts of concentrated sulfuric acid (96wt%), polycondensation reaction 7h, after the reaction, stand and separate layers, take the upper oil phase, wash with deionized water to neutral, pour the oil phase washed to neutral into 500ml In a dry four-necked flask, in a nitrogen atmosphere, reflux at 90°C for 2 hours, add 0.02 parts of potassium hydroxide, and react for 2 hours. After the reaction, cool and add acetic acid for neutralization under stirring. The filtered oil phase was distilled at 60°C for 3 hours under a nitrogen atmosphere, and the concentrated product obtained from the distillation was poured into a petri dish, and the low boilers were removed at 100°C / -0.1MPa to obtain a colorless and transparent product with h...
Embodiment 2
[0049] Add 40 parts of phenyltrimethoxysilane, 400 parts of toluene, and 150 parts of deionized water into a 500ml dry four-neck flask, stir rapidly at 20°C under a nitrogen atmosphere, perform hydrolysis reaction for 5 hours, heat up to 85°C, add 6 parts of concentrated sulfuric acid (96wt%), polycondensation reaction 7h, after the reaction finishes, stand to separate layers, take the upper oil phase, wash with deionized water to neutrality, pour the oily phase washed to neutrality into 500ml dry four In a nitrogen atmosphere, reflux at 80°C for 2 hours, add, for example, 0.2 parts of tetramethylammonium hydroxide, and react for 2 hours. After the reaction, cool and add acetic acid under stirring for neutralization. After the neutralization is completed, suction filter. The filtered oil phase was distilled at 100°C for 1 hour under nitrogen atmosphere, and the concentrated product obtained from the distillation was poured into a petri dish, and the low boilers were removed at ...
Embodiment 3
[0051] Add 40 parts of phenyltrimethoxysilane, 100 parts of tetrahydrofuran, 100 parts of isopropanol, and 150 parts of deionized water into a 500ml dry four-neck flask, stir rapidly at 80°C under nitrogen atmosphere, and hydrolyze for 0.5h , heat up to 100°C, add 6 parts of hydrochloric acid (36.5wt%), polycondensation reaction for 3h, after the reaction, stand and separate layers, take the upper oil phase, wash with deionized water until neutral, wash with water until neutral oil Pour the phase into a 500ml dry four-neck flask, reflux at 75°C for 2 hours in a nitrogen atmosphere, add 0.08 parts of potassium hydroxide, and react for 2 hours. After the reaction is completed, cool and add acetic acid to neutralize under stirring. Suction filtration, distill the filtered oil phase at 70°C for 2 hours under nitrogen atmosphere, pour the concentrated product obtained from the distillation into a petri dish, remove low boiling substances at 100°C / -0.1MPa, and obtain a colorless and ...
PUM
| Property | Measurement | Unit |
|---|---|---|
| refractive index | aaaaa | aaaaa |
| transmittivity | aaaaa | aaaaa |
Abstract
Description
Claims
Application Information
Login to View More - R&D
- Intellectual Property
- Life Sciences
- Materials
- Tech Scout
- Unparalleled Data Quality
- Higher Quality Content
- 60% Fewer Hallucinations
Browse by: Latest US Patents, China's latest patents, Technical Efficacy Thesaurus, Application Domain, Technology Topic, Popular Technical Reports.
© 2025 PatSnap. All rights reserved.Legal|Privacy policy|Modern Slavery Act Transparency Statement|Sitemap|About US| Contact US: help@patsnap.com