C08G77/392

MODIFIED POLYSILOXANE AND APPLICATION THEREOF
20210040268 · 2021-02-11 ·

A modified polysiloxane has formula (I)

##STR00001##

In formula (I) m is an integer between 0 and 10000; n is an integer between 0 and 10000; m and n cannot be equal to 0 simultaneously; R.sub.1-R.sub.7 are the same or different; and at least one of R.sub.1-R.sub.7 includes a group having a reversible chemical bond system based on a hydrogen bond, a coordinate bond, or a covalent bond. The polysioxane is used as a main chain to introduce a reversible chemical bond having temperature sensitivity by using a chemical method, so as to obtain a polymer material which is highly sensitive to temperature. The temperature-sensitive properties of materials provide functional materials for specific applications, such as medical external fixation materials, orthopedic materials, and packaging materials, can be obtained by using particular processing and preparation methods.

Silicone polymer and composition comprising the same

Provided is a composition comprising: (A) a silicone polymer of the Formula (I):
M.sup.1.sub.aM.sup.2.sub.bM.sup.3.sub.cD.sup.1.sub.dD.sup.2.sub.eD.sup.3.sub.fT.sup.1.sub.gT.sup.2.sub.hT.sup.3.sub.iQ.sub.j. wherein: M.sup.1=R.sup.1R.sup.2R.sup.3SiO.sub.1/2 M.sup.2=R.sup.4R.sup.5R.sup.6SiO.sub.1/2 M.sup.3=R.sup.7R.sup.8R.sup.9SiO.sub.1/2 D.sup.1=R.sup.10R.sup.11SiO.sub.2/2 D.sup.2=R.sup.12R.sup.13SiO.sub.2/2 D.sup.3=R.sup.14R.sup.15SiO.sub.2/2 T.sup.1=R.sup.16SiO.sub.3/2 T.sup.2=R.sup.17SiO.sub.3/2 T.sup.3=R.sup.18SiO.sub.3/2 Q=SiO.sub.4/2 where R.sup.1, R.sup.2, R.sup.3, R.sup.5, R.sup.6, R.sup.8, R.sup.9, R.sup.10, R.sup.11, R.sup.13, R.sup.15, R.sup.16 are independently chosen from a hydrogen, a C.sub.1-C.sub.60 aliphatic or aromatic group or C.sub.1-C.sub.60 alkoxy group; R.sup.4, R.sup.12, R.sup.17 are independently chosen from a C1-C10 alkyl, a C1-C10 alkoxy, or R.sup.19-A-R.sup.20 where A is chosen from a group comprising an unsaturated cyclic moiety chosen from an aromatic group, a fused aromatic group, an unsaturated alicyclic group, an unsaturated heterocyclic group, or a combination of two or more thereof; R.sup.19 is chosen from a H, a C1-C10 alkyl, allyl, vinyl, alkoxy, allyloxy, vinyloxy, acrylate, or methacrylate; and R.sup.20 is chosen from a divalent organic group; R.sup.7, R.sup.14, R.sup.18 are independently selected from hydrogen or OR.sup.22 or unsaturated monovalent radicals or radicals containing heteroatom such as oxygen, nitrogen, sulfur or radicals containing organosilane groups; and
the subscripts a, b, c, d, e, f, g, h, i, j are zero or positive subject to the following limitations: 2a+b+c+d+e+f+g+h+i+j1000, b+e+h>0 and c+f+i0 and
B) a thermally conductive filler.

Silicone polymer and composition comprising the same

Provided is a composition comprising: (A) a silicone polymer of the Formula (I):
M.sup.1.sub.aM.sup.2.sub.bM.sup.3.sub.cD.sup.1.sub.dD.sup.2.sub.eD.sup.3.sub.fT.sup.1.sub.gT.sup.2.sub.hT.sup.3.sub.iQ.sub.j. wherein: M.sup.1=R.sup.1R.sup.2R.sup.3SiO.sub.1/2 M.sup.2=R.sup.4R.sup.5R.sup.6SiO.sub.1/2 M.sup.3=R.sup.7R.sup.8R.sup.9SiO.sub.1/2 D.sup.1=R.sup.10R.sup.11SiO.sub.2/2 D.sup.2=R.sup.12R.sup.13SiO.sub.2/2 D.sup.3=R.sup.14R.sup.15SiO.sub.2/2 T.sup.1=R.sup.16SiO.sub.3/2 T.sup.2=R.sup.17SiO.sub.3/2 T.sup.3=R.sup.18SiO.sub.3/2 Q=SiO.sub.4/2 where R.sup.1, R.sup.2, R.sup.3, R.sup.5, R.sup.6, R.sup.8, R.sup.9, R.sup.10, R.sup.11, R.sup.13, R.sup.15, R.sup.16 are independently chosen from a hydrogen, a C.sub.1-C.sub.60 aliphatic or aromatic group or C.sub.1-C.sub.60 alkoxy group; R.sup.4, R.sup.12, R.sup.17 are independently chosen from a C1-C10 alkyl, a C1-C10 alkoxy, or R.sup.19-A-R.sup.20 where A is chosen from a group comprising an unsaturated cyclic moiety chosen from an aromatic group, a fused aromatic group, an unsaturated alicyclic group, an unsaturated heterocyclic group, or a combination of two or more thereof; R.sup.19 is chosen from a H, a C1-C10 alkyl, allyl, vinyl, alkoxy, allyloxy, vinyloxy, acrylate, or methacrylate; and R.sup.20 is chosen from a divalent organic group; R.sup.7, R.sup.14, R.sup.18 are independently selected from hydrogen or OR.sup.22 or unsaturated monovalent radicals or radicals containing heteroatom such as oxygen, nitrogen, sulfur or radicals containing organosilane groups; and
the subscripts a, b, c, d, e, f, g, h, i, j are zero or positive subject to the following limitations: 2a+b+c+d+e+f+g+h+i+j1000, b+e+h>0 and c+f+i0 and
B) a thermally conductive filler.

Room-temperature-curable organopolysiloxane composition and base material

The present invention pertains to a room-temperature-curable organopolysiloxane composition containing (A) an organopolysiloxane having the hydrolyzable silyl-group-containing monovalent organic group represented by formula (1) ##STR00001## (R.sup.1 represents a substituted or unsubstituted C1-10 alkyl group or a substituted or unsubstituted C6-10 aryl group, R.sup.2 represents a substituted or unsubstituted C1-10 alkyl group or a substituted or unsubstituted C6-10 aryl group, and R.sup.3 represents a substituted or unsubstituted C1-20 alkyl group or a hydrogen atom; M is an integer from 1 to 3, and n is an integer of 2 or more; and the broken line represents atomic bonding), (B) a hydrolyzable organosilane compound and/or a partially hydrolyzed condensate thereof, (C) a curing catalyst, and (F) a bleed oil. According to this configuration, an organotin-compound-free and MEKO-free product is achieved, exceptional fast-curing properties are achieved, and a cured coating film has exceptional rubber strength and exceptional antifouling performance over a long period of time.

Room-temperature-curable organopolysiloxane composition and base material

The present invention pertains to a room-temperature-curable organopolysiloxane composition containing (A) an organopolysiloxane having the hydrolyzable silyl-group-containing monovalent organic group represented by formula (1) ##STR00001## (R.sup.1 represents a substituted or unsubstituted C1-10 alkyl group or a substituted or unsubstituted C6-10 aryl group, R.sup.2 represents a substituted or unsubstituted C1-10 alkyl group or a substituted or unsubstituted C6-10 aryl group, and R.sup.3 represents a substituted or unsubstituted C1-20 alkyl group or a hydrogen atom; M is an integer from 1 to 3, and n is an integer of 2 or more; and the broken line represents atomic bonding), (B) a hydrolyzable organosilane compound and/or a partially hydrolyzed condensate thereof, (C) a curing catalyst, and (F) a bleed oil. According to this configuration, an organotin-compound-free and MEKO-free product is achieved, exceptional fast-curing properties are achieved, and a cured coating film has exceptional rubber strength and exceptional antifouling performance over a long period of time.

FUNCTIONALIZED Q-T-SILOXANE-BASED POLYMERIC MATERIALS WITH LOW SILOXANE RING CONTENT, SPECIFIC DEGREE OF POLYMERIZATION, AND METHOD FOR PREPARING SAME
20230416467 · 2023-12-28 ·

The present invention pertains to a functionalized polymeric liquid polysiloxane material comprising non-organofunctional Q-type siloxane moieties and mono-organofunctional T-type siloxane moieties, wherein the material comprises a limited low amount of four-membered Q.sup.2-type and/or Q.sup.3-type siloxane ring species relative to the total Q-type siloxane species, and has a functionalization-specific degree of polymerization as well as T- to Q-type ratio. The present invention further pertains to methods for producing the polymeric liquid polysiloxane material as well as associated uses of the material.

FUNCTIONALIZED Q-T-SILOXANE-BASED POLYMERIC MATERIALS WITH LOW SILOXANE RING CONTENT, SPECIFIC DEGREE OF POLYMERIZATION, AND METHOD FOR PREPARING SAME
20230416467 · 2023-12-28 ·

The present invention pertains to a functionalized polymeric liquid polysiloxane material comprising non-organofunctional Q-type siloxane moieties and mono-organofunctional T-type siloxane moieties, wherein the material comprises a limited low amount of four-membered Q.sup.2-type and/or Q.sup.3-type siloxane ring species relative to the total Q-type siloxane species, and has a functionalization-specific degree of polymerization as well as T- to Q-type ratio. The present invention further pertains to methods for producing the polymeric liquid polysiloxane material as well as associated uses of the material.

Method for manufacturing PDMS device and PDMS device manufactured thereby

A method for manufacturing a PDMS device in accordance with an exemplary embodiment of the present invention surface treats the entire surface of a pattern with a thiol group (SH), so that a hydrogel may be connected to the surface of the pattern by a covalent bond under ultraviolet rays. Therefore, a PDMS device manufactured by the above method has an advantage in that the shape thereof may be stably maintained without the swelling or desorption of a hydrogel even when an electrolyte is filled in a pattern.

Method for manufacturing PDMS device and PDMS device manufactured thereby

A method for manufacturing a PDMS device in accordance with an exemplary embodiment of the present invention surface treats the entire surface of a pattern with a thiol group (SH), so that a hydrogel may be connected to the surface of the pattern by a covalent bond under ultraviolet rays. Therefore, a PDMS device manufactured by the above method has an advantage in that the shape thereof may be stably maintained without the swelling or desorption of a hydrogel even when an electrolyte is filled in a pattern.

HYDROPHILIZED POLYDIORGANOSILOXANE VINYLIC CROSSLINKERS AND USES THEREOF
20210009743 · 2021-01-14 ·

The invention provides a hydrophilized polydiorganosiloxane vinylic crosslinker which comprises (1) a polydiorganosiloxane polymer chain comprising dimethylsiloxane units and hydrophilized siloxane units each having one methyl substituent and one monovalent C.sub.4-C.sub.40 organic radical substituent having two to six hydroxyl groups, wherein the molar ratio of the hydrophilized siloxane units to the dimethylsiloxane units is from about 0.035 to about 0.15, and (2) two terminal (meth)acryloyl groups. The hydrophilized polydiorganosiloxane vinylic crosslinker has a number average molecular weight of from about 3000 Daltons to about 80,000 Daltons. The present invention is also related to a silicone hydrogel contact lens, which comprises repeating units derived from a hydrophilized polydiorganosiloxane vinylic crosslinker of the invention.