Polydiorganosiloxane preparation

US12378362B2 · US · B2

Patent metadata
FieldValue
Publication numberUS-12378362-B2
Application numberUS-201917786389-A
CountryUS
Kind codeB2
Filing dateDec 17, 2019
Priority dateDec 17, 2019
Publication dateAug 5, 2025
Grant dateAug 5, 2025

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  1. Title

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  2. Abstract

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  3. Assignees and inventors

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  4. Key dates

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  5. First independent claim

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  6. CPC / IPC classifications

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  7. Citations and related patents

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Abstract

Official abstract text for this publication.

A process for end capping and chain extending silanol terminated polydiorganosiloxanes with a mixture of one or more alkylacetoxydialkoxysilanes and one or more alkyldiacetoxyalkoxysilanes. The resulting capped polymeric material may be utilised as a polymer in e.g. a one-part alkoxy sealant composition such as, for example, an alkoxy low modulus clean (non-staining) or clear sealant composition.

First claim

Opening claim text (preview).

What is claimed is: 1. A process for preparing a chain-extended alkoxy polydiorganosiloxane from a silanol terminated polydiorganosiloxane starting material, the process: (i) reacting the silanol terminated polydiorganosiloxane starting material with a mixture of one or more alkylacetoxydialkoxysilanes and one or more alkyldiacetoxyalkoxysilanes wherein each alkyl group may be the same or different and contains from 1 to 6 carbons and each alkoxy group may be the same or different and contains from 1 to 6 carbons; and (ii) neutralising the resulting mixture from step (i). 2. The process for preparing a chain-extended alkoxy polydiorganosiloxane in accordance with claim 1 , wherein each alkylacetoxydialkoxysilane comprises an alkyl group having from 1 to 6 carbons and two alkoxy groups each of which contain from 1 to 6 carbons. 3. The process for preparing a chain-extended alkoxy polydiorganosiloxane in accordance with claim 1 , wherein each alkyldiacetoxyalkoxysilane comprises an alkyl group having from 1 to 6 carbons and an alkoxy group containing from 1 to 6 carbons. 4. The process for preparing a chain-extended alkoxy polydiorganosiloxane in accordance with claim 1 , wherein in step (i) the silanol terminated polydiorganosiloxane starting material is reacted with a mixture of methylacetoxydimethoxysilane and methyldiacetoxymethoxysilane. 5. The process for preparing a chain-extended alkoxy polydiorganosiloxane in accordance with claim 1 , wherein a neutralising agent is utilised in step (ii) and is selected from the group consisting of hexylamine, dodecylamine, di-n-hexylamine, 2-ethylhexylamine, tert-butylamine, 2-ethylhexylamine, 1,6-hexanediamine, bis(2-ethylhexyl)amine, morpholine, dicyclohexylamine, 1,8-Diazabicyclo(5.4.0)undec-7-ene (DBU), (3-aminopropyl)-triethoxysilane, (3-aminopropyl)-trimethoxysilane, aminoethylaminopropyltrimethoxysilane bis(trimethoxysilylpropyl)amine, (dimethoxymethylsilyl)isobutyl)-ethylenediamine, dialkyldiacetamidosilanes, and combinations thereof. 6. The process for preparing a chain-extended alkoxy polydiorganosiloxane in accordance with claim 1 , wherein a neutralising agent is utilised in step (ii) and is a dialkyldiacetamidosilane selected from N,N′-(dimethylsilylene)bis[N-ethylacetamide] and/or N,N′-(dimethylsilylene)bis[N-methylacetamide]. 7. The process for preparing a chain-extended alkoxy polydiorganosiloxane in accordance with claim 1 , wherein components of the reaction process are present in the following amounts: (ai) silanol terminated polydiorganosiloxane starting material in an amount of from 95 to 99.5% by weight of the ingredients; (aii) mixture of one or more alkylacetoxydialkoxysilanes and one or more alkyldiacetoxyalkoxysilanes in an amount of from about 0.25 to 2.55 by weight of the ingredients; and (aiii) neutralising agent in an amount of from about 0.25 to 2.5 % by weight of the ingredients. 8. The process for preparing a chain-extended alkoxy polydiorganosiloxane in accordance with claim 1 , wherein once step (ii) has completed, the resulting polymeric product is collected and stored for future use or utilised in a process for preparing a one-part low modulus sealant composition, the sealant composition comprising: (a) the chain-extended alkoxy terminated polydiorganosiloxane; (b) reinforcing filler; (c) cross-linker; and (d) cure catalyst; and optionally (e) adhesion promoter. 9. An alkoxy end-capped, chain extended polydiorganosiloxane polymer obtained from the process of claim 1 . 10. A one-part low modulus sealant composition comprising: (a) a chain-extended alkoxy terminated polydiorganosiloxane; (b) reinforcing filler; (c) cross-linker; and (d) cure catalyst; and optionally (e) adhesion promoter; wherein component (a) obtained from the process of claim 1 . 11. The one-part low modulus sealant composition in accordance with claim 10 , wherein cure catalyst (d) is selected from the group consisting of: (i) a chelated titanate catalyst; (ii) a chelated zirconate catalyst; (iii) an optionally chelated titanate in combination with a metal carboxylate salt; and/or (iv) an optionally chelated zirconate in combination with a metal carboxylate salt; and combinations thereof; optionally, wherein cure catalyst (d) additionally includes (v) a tin catalyst. 12. The one-part low modulus sealant composition in accordance with claim 10 , which is gunnable and/or self-levelling. 13. The one-part low modulus sealant composition in accordance with claim 10 , capable of being applied as a paste to a joint between two adjacent substrate surfaces where it can be worked, prior to curing, to provide a smooth surfaced mass which will remain in its allotted position until it has cured into an elastomeric body adherent to the adjacent substrate surfaces. 14. A silicone elastomer which is the reaction product of the one-part low modulus sealant composition in accordance with claim 10 . 15. A sealant suitable for use in the facade, insulated glass, window construction, automotive, solar and construction fields, wherein the sealant comprises or is formed from the one-part low modulus sealant composition in accordance with claim 10 . 16. A method for filling a space between two substrates so as to create a seal therebetween, the method comprising: a) providing the one-part low modulus sealant composition in accordance with claim 10 ; and either b) or c); b) applying the sealant composition to a first substrate, and bringing a second substrate in contact with the sealant composition that has been applied to the first substrate, or c) filling a space formed by the arrangement of a first substrate and a second substrate with the sealant composition and curing the sealant composition. 17. The method for filling a space between two substrates in accordance with claim 16 , wherein the space is filled by introducing the sealant composition by way of extrusion or through a sealant gun.

Assignees

Inventors

Classifications

  • containing silicon bound to oxygen-containing groups (C09J183/12 takes precedence) · CPC title

  • Calcium, strontium or barium carbonate · CPC title

  • Carbonates; Bicarbonates · CPC title

  • C08G77/18Primary

    to alkoxy or aryloxy groups · CPC title

  • Preparatory processes · CPC title

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What does patent US12378362B2 cover?
A process for end capping and chain extending silanol terminated polydiorganosiloxanes with a mixture of one or more alkylacetoxydialkoxysilanes and one or more alkyldiacetoxyalkoxysilanes. The resulting capped polymeric material may be utilised as a polymer in e.g. a one-part alkoxy sealant composition such as, for example, an alkoxy low modulus clean (non-staining) or clear sealant composition.
Who is the assignee on this patent?
Dow Silicones Corp
What technology area does this patent fall under?
Primary CPC classification C08G77/18. Mapped technology areas include Chemistry & Metallurgy.
When was this patent published?
Publication date Tue Aug 05 2025 00:00:00 GMT+0000 (Coordinated Universal Time) (B2). Legal status and post-grant events are not shown on this page.
What related patents are in patentsdb?
We list 8 related publications on this page (citations in our corpus or others sharing the same primary CPC).