Thermal conducting silicone polymer composition
A composition and polymer technology, applied in coatings, adhesives, additive processing, etc., can solve the problems of affecting the elastomer properties of thermal interface materials, reducing the fluidity of composite materials, and high adhesion layer thickness.
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Embodiment 1
[0129]Example 1: Diphenylsulfone functionalized polyorganosiloxane with terminal allyloxy ether groups (A1)
[0130]In a nitrogen environment, in a three-necked round bottom flask equipped with a reflux condenser, dropping funnel and mechanical stirrer, allyloxydiphenyl sulfone (16.9g, 0.051mol) and Karstedt catalyst (5ppm 2wt% Pt ) In a toluene (100 mL) solution, add polydimethylsiloxane (334.52 g, 0.151 mol) with terminal hydride groups (Hyd equivalent 0.952) dropwise within 30 min. Increase the reaction temperature to 85°C and continue until all hydride peaks change from1H-NMR disappeared. The resulting allyloxy ether-terminated polymer was vacuum stripped at 150 degrees Celsius for 3 hours to remove volatile compounds and solvents. The obtained product is a high viscosity liquid. (GPC: Mn=12392, PDI-1.8; viscosity: 6Pa.S).
Embodiment 2
[0131]Example 2: Diphenylsulfone functionalized polyorganosiloxane with terminal hydride groups
[0132]At 75℃, to the toluene (150mL) solution of allyloxydiphenyl sulfone (25g, 0.076mol) and Karstedt catalyst (0.09g, 5ppm2wt% Pt), the terminal hydride was added dropwise within 30 minutes Group (hydride equivalent 0.952) polydimethylsiloxane (334.52g, 0.151mol). Then the reaction temperature was increased to 85°C and continued until all the allyl peaks changed from1H-NMR disappeared. The resulting hydride-terminated polymer was vacuum stripped at 150 degrees Celsius for 3 hours to remove volatile compounds and solvents. The obtained product is a low-viscosity liquid. (GPC: Mn= 3069 g / mol, PDI-1.7; viscosity: 0.33 Pa.S).
Embodiment 3
[0133]Example 3 (A2): Diphenylsulfone functionalized polyorganosiloxane with terminal vinyl groups
[0134]To the reaction mixture of hydride-terminated diphenylsulfone functionalized polyorganosiloxane (71.9 g) (obtained in Example 3), toluene (30 mL) and platinum catalyst (5 ppm 2% Pt) was added 1,3 -Divinyltetramethyldisiloxane (8.88g, 0.048mol) and reflux at 110 degrees Celsius. Continue the reaction until all hydride signals change from1H-NMR disappeared. Finally, the resulting polymer was vacuum stripped at 150 degrees Celsius for 3 hours to remove volatile compounds and solvents. The final product obtained is a low-viscosity liquid. (GPC: Mn=5014 g / mol, PDI-1.9; viscosity: 0.56 Pa.S).
[0135]Preparation of thermally conductive silicone composition
[0136]Purchase alumina filler with a size of 0.3-110 microns from Sumitomo. Purchase boron nitride fillers with sizes ranging from 5 to 400μ from Momentive Performance Materials.
[0137]By mixing vinyl-terminated dimethylsiloxane copolymer ...
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