Crosslinkable fluoropolymers
US-2016369028-A1 · Dec 22, 2016 · US
US12528901B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-12528901-B2 |
| Application number | US-202217696350-A |
| Country | US |
| Kind code | B2 |
| Filing date | Mar 16, 2022 |
| Priority date | Sep 17, 2019 |
| Publication date | Jan 20, 2026 |
| Grant date | Jan 20, 2026 |
A practical reading order for non-experts. Skip the full description unless you need deep technical detail.
What the patent document calls the invention.
A short plain-language summary of the technical disclosure.
Who owns or filed the patent and who is credited as inventor.
Filing, priority, publication, and grant dates set the timeline.
The legal scope of protection — read this for what is actually claimed.
Technology tags used to group this patent with similar filings.
Prior art links and similar publications in this corpus.
Official abstract text for this publication.
A modified polymer including (a) a main chain containing a fluorine-containing polymer and (b) a side chain represented by the following formula (b1′) and/or a side chain represented by the following formula (b2′). The formula (b1′) is —CH 2 —CR b1 (—X)—C(═O)—Y—Z—Rf, wherein X is a hydrogen atom, a methyl group, or a halogen atom; Y is —O— or —NH—; Z is a direct bond or a divalent organic group; Rf is a C1-C20 fluoroalkyl group; and R b1 is a hydrogen atom or a monovalent organic group. The formula (b2′) is —CH 2 —CR b2 (—R 1 )—C(═O)—O—Si(—CH 3 ) 2 —[O—Si(—CH 3 ) 2 ] n —O—Si(—CH 3 ) 2 —R 2 , wherein R 1 is a hydrogen atom or a methyl group; R 2 is a hydrogen atom or a methyl group; R b2 is a hydrogen atom or a monovalent organic group; and n is 3 to 200.
Opening claim text (preview).
What is claimed is: 1 . A modified polymer comprising: (a) a main chain containing a fluorine-containing polymer, containing a unit represented by —CHR—, wherein R is a hydrogen atom or a monovalent organic group, and containing a polymerized unit based on tetrafluoroethylene or chlorotrifluoroethylene; and (b) a side chain represented by the following formula (b2′), or a side chain represented by the following formula (b1′) and a side chain represented by the following formula (b2′), the formula (b1′) being: —CH 2 —CR b1 (—X)—C(═O)—Y—Z—Rf (b1′) wherein X is a hydrogen atom, a methyl group, or a halogen atom; Y is —O— or —NH—; Z is a direct bond or a divalent organic group; Rf is a C1-C20 fluoroalkyl group; and R b1 is a hydrogen atom or a monovalent organic group, the formula (b2′) being: —CH 2 —CR b2 (—R 1 )—C(═O)—O—Si(—CH 3 ) 2 —[O—Si(—CH 3 ) 2 ] n —O—Si(—CH 3 ) 2 —R 2 (b2′) wherein R 1 is a hydrogen atom or a methyl group; R 2 is a hydrogen atom or a methyl group; R b2 is a hydrogen atom or a monovalent organic group; and n is 3 to 200. 2 . A composition comprising the modified polymer according to claim 1 . 3 . The composition according to claim 2 , further comprising a solvent. 4 . The composition according to claim 2 , further comprising a curing agent. 5 . The composition according to claim 2 , wherein the composition is a coating material. 6 . The composition according to claim 2 , wherein the composition is a composition for freeze prevention and/or frost prevention. 7 . A coating film obtained by applying the composition according to claim 2 . 8 . The coating film according to claim 7 , wherein the coating film has a water contact angle of 95° or greater and a gloss retention of 80% or higher after 3000-hour QUVB testing. 9 . The coating film according to claim 7 , wherein the coating film has a water contact angle of 80° or greater after 1000-hour QUVB testing and an oil contact angle of 25° or greater after 1000-hour QUVB testing. 10 . A laminate comprising a substrate and the coating film according to claim 7 . 11 . A coating material, comprising: the modified polymer according to claim 1 ; and a solvent. 12 . The coating material according claim 11 , wherein the solvent is at least one selected from the group consisting of esters, aliphatic hydrocarbons, alcohols, and cyclic ethers. 13 . The coating material according claim 11 , wherein the fluorine-containing polymer in the main chain further comprises a unit, a vinyl ester unit containing neither a hydroxy group nor an aromatic ring, and/or a hydroxy group-containing monomer unit. 14 . The coating material according claim 11 , wherein the solvent is at least one selected from the group consisting of esters, aliphatic hydrocarbons, alcohols, and cyclic ethers, and wherein the fluorine-containing polymer in the main chain further comprises a vinyl ester unit containing neither a hydroxy group nor an aromatic ring, and/or a hydroxy group-containing monomer unit. 15 . A modified polymer according to claim 1 , comprising: (b) a side chain represented by the formula (b1′) and a side chain represented by the formula (b2′).
grafted on to macromolecular compounds obtained by reactions only involving unsaturated carbon-to-carbon bonds (C09D151/04, C09D151/06 take precedence) · CPC title
leading to a crosslinking, either explicitly or inherently · CPC title
Chemical modification by after-treatment (graft polymers, block polymers, crosslinking with unsaturated monomers or with polymers C08F251/00 - C08F299/00; of conjugated diene rubbers C08C) · CPC title
Introducing metal atoms or metal-containing groups · CPC title
with non-fluorinated vinyl ethers · CPC title
Related publications grouped by family.
Answers are generated from the same data shown on this page.