Organopolysiloxane composition, and half-cured product and cured product produced from same

Active Publication Date: 2021-06-17
DOW TORAY CO LTD
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Benefits of technology

[0015]The present invention is able to provide a composition that has a sufficient pot life at room temperature, that can be cured at low temperature once initiated by exposure to high energy radiation, and that produces a viscous or a thermoplastic material during the curing process. Here, the portions shielded from exposure to high energy radiation can be cured over time.
[0016]A composition of the present invention contains components (A) to (D) below. They will now be described in order.
[0017]A composition of the present invention includes a compound containing at least one aliphatically unsaturated monovalent hydrocarbon group in the molecule (component (A)). Component (A) is a compound containing an aliphatically unsaturated monovalent hydrocarbon group to which a hydrosilyl group (—SiH) is added during the hydrosilylation reaction. Examples of compound (A) include alkenyl group-containing linear or branched organopolysiloxanes, alkenyl group-containing polyethers, alkenyl group-containing polyolefins, and alkenyl group-containing polyesters. Among these, organopolysiloxanes represented by average composition formula (1) below are preferred.
[0018]In general formula (1), R1 is an alkenyl group having from 2 to 12 carbon atoms. Specific examples include a vinyl group, allyl group, butenyl group, pentenyl group, hexenyl group, heptenyl group, octenyl group, nonenyl group, decenyl group, undecenyl group, and dodecenyl group. Among these, a vinyl group, an allyl group or a hexenyl group is preferred. R2 is a group selected from among an aliphatic unsaturated bond-free monovalent hydrocarbon group, hydroxyl group and alkoxy group having from 1 to 12 carbon atoms. In th

Problems solved by technology

However, when a silicone material is formed on a substrate such as a thermoplastic resin film, the substrate cannot be subjected to high temperatures.
However, organopolysiloxane compositions that use high energy radiation activated catalysts are not cured immediately even when exposed to high energy radiation.
When heat is applied to cure a composition in a shorter period of time or the amount of catalyst used is increased to cure a composition in a shorter period of time, the cured product may become discolored.
When curing is performed at a lower temperature

Method used

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Examples

Experimental program
Comparison scheme
Effect test

example 1

[0077]A composition was prepared comprising: 3.5 parts by weight of a vinyl-capped branched polysiloxane (A-1) represented by the average composition formula: (Me2ViSiO1 / 2)0.044(Me3SiO1 / 2)0.411(SiO4 / 2)0.545; 89.7 parts by weight of a vinyl-capped linear polysiloxane (A-2) represented by the average composition formula: ViMe2SiO(SiMe2O)322SiMe2Vi; 6.8 parts by weight of a linear polysiloxane (B-1) represented by the average composition formula: HMe2SiO(SiMe2O)10SiMe2H; 5 ppm of a platinum-1,3-divinyl-1,1,3,3-tetramethyldisiloxane complex (C-1) in terms of platinum atoms; and 20 ppm of (methylcyclopentadienyl) trimethylplatinum (IV) (D-1) in terms of platinum atoms. The viscosity of the composition was 1,800 mPa·s. After preparing the composition and allowing it to stand for 10 minutes to reach a viscosity of 3,200 mPa·s, the composition was exposed via an ozone cut filter to a 2 W high-pressure mercury lamp at a 365-nm UV exposure level of 5,000 mJ / cm2. The viscosity measured im

example 2

[0078]A composition was prepared comprising: 3.5 parts by weight of A-1; 6.5 parts by weight of A-2; 82.4 parts by weight of a vinyl-capped linear polysiloxane (A-3) represented by the average composition formula: ViMe2SiO(SiMe2O)535SiMe2Vi; 4.6 parts by weight of B-1; 10 ppm of C-1 in terms of platinum atoms; and 20 ppm of D-1 in terms of platinum atoms. The viscosity of the composition was 8,200 mPa·s. After preparing the composition and allowing it to stand for 10 minutes to reach a viscosity of 14,000 mPa·s, the composition was exposed via an ozone cut filter to a 2 W high-pressure mercury lamp at a 365-nm UV exposure level of 2,500 mJ / cm2. The viscosity measured immediately thereafter was above 50,000 mPa·s, but the composition remained fluid. It became a non-fluid gel after 10 more minutes of UV exposure. When the hardness of the cured product was measured by penetration every 10 minutes, the hardness stabilized at a penetration of 35 after one hour of UV exposure indicating th

example 3

[0079]A composition was prepared comprising: 55.7 parts by weight of a vinyl-capped branched polysiloxane (A-4) represented by the average composition formula: (Me2ViSiO1 / 2)0.1(Me3SiO1 / 2)0.4(SiO4 / 2)0.5; 13.3 parts by weight of a branched polysiloxane (E-1) represented by the average composition formula: (Me3SiO1 / 2)0.44(SiO4 / 2)0.56; 1.7 parts by weight of a vinyl-capped linear polysiloxane (A-3) represented by the average composition formula: ViMe2SiO(SiMe2O)160SiMe2Vi; 24.6 parts by weight of a linear polysiloxane (B-2) represented by the average composition formula: HMe2SiO(SiMe2O)400SiMe2H; 4.7 parts by weight of a linear polysiloxane (B-3) represented by the average composition formula: Me3SiO(SiMe2O)30(SiMeHO)30SiMe3; 0.2 ppm of C-1 in terms of platinum atoms; and 5 ppm of D-1 in terms of platinum atoms. The viscosity of the composition was 3,500 mPa·s. The composition was heated for 30 minutes at 90° C. A thermoplastic material was obtained that was not fluid at 25° C. b

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Abstract

Provided is a hydrosilylation reactive composition that has a sufficient pot life at room temperature, that can be cured at low temperature by exposure to high energy radiation, and that produces a stable semi-cured product during the curing process, and to provide a semi-cured product and a cured product obtained using this hydrosilylation reactive composition. The composition comprises: (A) a compound containing at least one aliphatically unsaturated monovalent hydrocarbon group in the molecule; (B) a compound containing at least two hydrogen atoms bonded to silicon atoms in the molecule; (C) a first hydrosilylation catalyst exhibiting activity in the composition without exposure to high energy radiation; and (D) a second hydrosilylation catalyst not exhibiting activity unless exposed to high energy radiation, and exhibiting activity in the composition by exposure to high energy radiation.

Description

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Claims

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Application Information

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Owner DOW TORAY CO LTD
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