Liquid conductive silastic used for electric stress control and preparation method thereof
A technology of conductive silicon and electrical stress, applied in the direction of conductive materials dispersed in non-conductive inorganic materials, etc., can solve the problems of physical and mechanical performance degradation, poor affinity, high cost, etc., and achieve good mechanical properties, convenient operation and short production cycle Effect
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Embodiment 1
[0034]Component A contains 80 parts by weight of organopolysiloxane, 60 parts of a blend of acetylene carbon black and fumed silica, 1.0 part of fluorosilicon multipolymer, and 0.2 parts of 3000ppm platinum catalyst; component B contains organopolysiloxane 80 parts by weight of oxane, 60 parts of acetylene carbon black and fumed silica blend, 1.0 part of fluorosilicon polypolymer, 0.2 part of butynol inhibitor, 4.0 parts by weight of organohydrogenpolysiloxane; Mix at 80°C for 8 hours, then heat to 175°C and evacuate for 2 hours, stir and cool through a three-roller mill, then mix components A and B evenly at a mass ratio of 1:1, remove foam, and make the product of the present invention. After 165℃ / 10min tablet test, comprehensive physical properties: hardness, Shore A: 38; tensile strength, Mpa: 5.7; tear strength, KN / m: 29; elongation at break, %: 560; volume resistivity , Ω cm: 182; dielectric constant: 2.8.
Embodiment 2
[0036] Component A contains 60 parts by weight of organopolysiloxane, 50 parts of a blend of acetylene carbon black and fumed silica, 0.5 parts of fluorosilicon multipolymer, and 0.2 parts of 3000ppm platinum catalyst; component B contains organopolysiloxane 60 parts by weight of oxane, 50 parts of acetylene carbon black and fumed silica blend, 2.0 parts of fluorosilicon polypolymer, 0.2 part of butynol inhibitor, 3.0 parts by weight of organohydrogenpolysiloxane; Mix at 110°C for 7 hours, then heat to 160°C and evacuate for 2 hours, stir and cool through a three-roller mill, and then mix A and B components uniformly at a mass ratio of 1:1 and remove foam to make the product of the present invention. After 165 ℃ / 10min tablet test comprehensive physical properties: hardness, Shore A: 35; tensile strength, Mpa: 5.6; tear strength, KN / m: 28; elongation at break, %: 570; volume resistivity , Ω·cm: 190; dielectric constant: 2.9.
Embodiment 3
[0038] Component A contains 35 parts by weight of organopolysiloxane, 40 parts of a blend of acetylene carbon black and fumed silica, 2.0 parts of fluorosilicon multipolymer, and 0.2 parts of 3000ppm platinum catalyst; component B contains organopolysiloxane 35 parts by weight of oxane, 40 parts of acetylene carbon black and fumed silica blend, 0.5 part of fluorosilicon polypolymer, 0.2 part of butynol inhibitor, 5.0 parts by weight of organohydrogen polysiloxane; Mix at 130°C for 8 hours, then heat to 150°C and evacuate for 3 hours, stir and cool through a three-roller mill, then mix components A and B evenly at a mass ratio of 1:1, and remove foam to make the product of the present invention. After 165 ℃ / 10min tablet test comprehensive physical properties: hardness, Shore A: 33; tensile strength, Mpa: 5.5; tear strength, KN / m: 30; elongation at break, %: 578; volume resistivity , Ω·cm: 195; dielectric constant: 3.0.
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