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Solventless cured release coating-forming organopolysiloxane composition and sheet-form substrate having cured release coating

A release coating, polysiloxane technology, applied in the direction of coatings, chemical instruments and methods, synthetic resin layered products, etc., can solve the problem of not realizing the friction coefficient of the cured coating, the increase in slidability, not mentioned Reduce the friction coefficient of the cured coating and other problems such as sliding, to achieve the effect of excellent residual adhesion, improved sliding, and improved peeling performance

Active Publication Date: 2012-10-10
DOW CORNING TORAY CO LTD +1
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

However, it is not recognized that the coefficient of friction of the cured coating decreases, and its slidability increases, nor does it mention a means of reducing the coefficient of friction of the cured coating and increasing its slidability

Method used

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Examples

Experimental program
Comparison scheme
Effect test

Synthetic example 1

[0059] Synthesis Example 1 Synthesis (1): (Vi(CH 3 ) 2 SiO 1 / 2 ) 4 (Vi(CH 3 ) SiO 2 / 2 ) 2 ((CH 3 ) 2 SiO) 54 (SiO 4 / 2 ) will [Vi(CH 3 ) 2 SiO 1 / 2 ] 4 SiO 4 / 2(21.6g), tetramethyltetravinylcyclotetrasiloxane (8.60g), octamethylcyclotetrasiloxane (200g) and trifluoromethanesulfonic acid (1.2g) were introduced into the reaction vessel, and Stir for 6 hours at a temperature of 80-90°C. The resulting reaction mixture was then cooled to room temperature. Calcium carbonate powder (1.0 g) was added to the cooled reaction mixture, followed by stirring for 3 hours and filtering. The filtrate was stripped for 2 hours at a pressure of 40 mbar (4000 Pa) and a temperature of about 150°C. The viscosity of the stripped residue was 46 mPa.s, and its vinyl content was 3.5% by weight.

Synthetic example 2

[0060] Synthesis Example 2 Synthesis (2): (Vi(CH 3 ) 2 SiO 1 / 2 ) 4 (Vi(CH 3 ) SiO 2 / 2 ) 1.8 ((CH 3 ) 2 SiO) 103 (SiO 4 / 2 ) will [Vi(CH 3 ) 2 SiO 1 / 2 ] 4 SiO 4 / 2 (21.6g), tetramethyltetravinylcyclotetrasiloxane (7.74g), octamethylcyclotetrasiloxane (381g) and trifluoromethanesulfonic acid (1.2g) were introduced into the reaction vessel, and Stir for 6 hours at a temperature of 80-90°C. The resulting reaction mixture was then cooled to room temperature. Calcium carbonate powder (1.0 g) was added to the cooled reaction mixture, followed by stirring for 3 hours and filtering. The filtrate was stripped for 2 hours at a pressure of 40 mbar (4000 Pa) and a temperature of about 150°C. The viscosity of the stripped residue was 122 mPa.s, and its vinyl content was 1.9% by weight.

Synthetic example 3

[0061] Synthesis Example 3 Synthesis (3): (Vi(CH 3 ) 2 SiO 1 / 2 ) 4 (Vi(CH 3 ) SiO 2 / 2 ) 21.9 ((CH 3 ) 2 SiO) 136 (SiO 4 / 2 ) will [Vi(CH 3 ) 2 SiO 1 / 2 ] 4 SiO 4 / 2 (21.6g), tetramethyltetravinylcyclotetrasiloxane (94.2g), octamethylcyclotetrasiloxane (503g) and trifluoromethanesulfonic acid (1.2g) were introduced into the reaction vessel, and Stir for 6 hours at a temperature of 80-90°C. The resulting reaction mixture was then cooled to room temperature. Calcium carbonate powder (1.0 g) was added to the cooled reaction mixture, followed by stirring for 3 hours and filtering. The filtrate was stripped for 2 hours at a pressure of 40 mbar (4000 Pa) and a temperature of about 150°C. The viscosity of the stripped residue was 111 mPa.s, and its vinyl content was 5.6% by weight.

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Abstract

A solventless, cured release coating-forming organopolysiloxane composition comprising (A) 100 parts of an organopolysiloxane fluid having a branched structure and comprising (i) the siloxane unit represented by the formula SiO4 / 2, (ii) the siloxane unit represented by the general formula R2SiO2 / 2, and (iii) the siloxane unit represented by the general formula RaR2SiO1 / 2; (B) 0.5 to 15 parts of a diorganopolysiloxane with the average structural formula RaRc 2SiO(RbRcSiO2 / 2)n1(Rc2SiO2 / 2)n2SiRc2Ra; (c) a predetermined amount of organohydrogenpolysiloxane; and (D) a hydrosililatingreaction catalyst. In additon, the sheet-form substrate has the cured coating thereon.

Description

technical field [0001] The present invention relates to solvent-free organopolysiloxane compositions forming cured release coatings which can be applied to substrates in the form of sheets such as paper, polyolefin-laminated paper, thermoplastic resin films, metal foils, etc. Forms a cured release coating on the surface of the surface; can provide excellent peeling performance with respect to sticky substances; and can provide a treated surface with smooth sliding properties. The invention also relates to a substrate in the form of a sheet with a cured release coating obtained by curing the composition. Background technique [0002] Addition reaction curable organopolysiloxane combination by dissolving an alkenyl functional diorganopolysiloxane gum, an organohydrogenpolysiloxane and a hydrosilylation reaction catalyst in an organic solvent such as toluene The solution-type organopolysiloxane composition prepared as a compound is well known, and is generally used for forming...

Claims

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Application Information

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Patent Type & Authority Patents(China)
IPC IPC(8): C08L83/04C09D183/04C09J7/02C08L83/07
CPCC09J2423/006C09J2483/005C09D183/04C09J2400/283C08L83/04C09J7/0228C09J7/401C08L83/00B32B27/28
Inventor 堀诚司山田高照D·A·里奇
Owner DOW CORNING TORAY CO LTD