Topical protective polymerized nanoparticles in an active or bioactive array, methods for preparing same and uses thereof
US-2015374610-A1 · Dec 31, 2015 · US
US2024209133A1 · US · A1
| Field | Value |
|---|---|
| Publication number | US-2024209133-A1 |
| Application number | US-202118556107-A |
| Country | US |
| Kind code | A1 |
| Filing date | Jun 30, 2021 |
| Priority date | Jun 30, 2021 |
| Publication date | Jun 27, 2024 |
| Grant date | — |
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 process to form a composition comprising a crosslinked olefin-based polymer derived from an anhydride-functionalized olefin-based polymer, said process comprising at least the following steps A) and B): A) mixing together at least the following components a and b to form a first composition: a) the anhydride-functionalized olefin-based polymer, and b) at least one epoxy-silane compound; B) exposing the first composition to moisture to form the crosslinked olefin-based polymer. The first compositions and crosslinked compositions are also disclosed.
Opening claim text (preview).
1 . A process to form a composition comprising a crosslinked olefin-based polymer derived from an “anhydride-functionalized olefin-based polymer,” said process comprising at least the following steps A) and B): A) mixing together at least the following components a and b to form a first composition: a) the “anhydride-functionalized olefin-based polymer,” and b) at least one epoxy-silane compound; B) exposing the first composition to moisture to form the crosslinked olefin-based polymer. 2 . The process of claim 1 , wherein the epoxy-silane compound is selected from structures e1) or e2) below: where R is an alkylene group or a CH 2 O-alkylene group, X1, X2 and X3 are each independently an alkoxy group or an alkyl group, and at least one of X1, X2 or X3 is an alkoxy group; or where R′ is an alkylene group or a CH 2 O-alkylene group, X4, X5 and X6 are each independently an alkoxy group or an alkyl group, and at least one of X4, X5 or X6 is an alkoxy group. 3 . The process of claim 1 , wherein the first composition, after seven days at 22° C., 50% RH, in air atmosphere, has SAFT value from 70° C. to 170° C. 4 . The process of claim 1 , wherein composition comprises either a crosslinked ethylene-based polymer derived from an anhydride-functionalized ethylene-based polymer, or a crosslinked propylene-based polymer derived from an anhydride-functionalized propylene-based polymer. 5 . The process of claim 1 , wherein composition comprises a crosslinked ethylene-based polymer derived from an anhydride-functionalized ethylene-based polymer. 6 . The process of claim 1 , wherein the first composition has a percent increase in melt viscosity at 120° C. (% Δη2 at 120° C.) from 1.0% to 25%; and where % Δη2 at 120° C.=[(η2−η1)/η1]×100, and where 2 is the melt viscosity after 2 hours at 120° C., and η1 is the melt viscosity after 1 hour at 120° C. 7 . The process of claim 1 , wherein, the first composition further comprises a tackifier (component c). 8 . A crosslinked composition formed from the process of claim 1 . 9 . A first composition comprising at least the following components a and b: a) an “anhydride-functionalized olefin-based polymer;” b) at least one epoxy-silane compound. 10 . The composition of claim 9 , wherein the epoxy-silane compound is selected from structures e1) or e2) below: where R is an alkylene group or a CH 2 O-alkylene group, X1, X2 and X3 are each independently an alkoxy group or an alkyl group, and at least one of X1, X2 or X3 is an alkoxy group; or where R′ is an alkylene group or a CH 2 O-alkylene group, X4, X5 and X6 are each independently an alkoxy group or an alkyl group, and at least one of X4, X5 or X6 is an alkoxy group. 11 . The composition of claim 9 , wherein the epoxy-silane compound is selected from structures e11), e12), e21), e22), e23), e24), e25), e26), e27) or e28) below: 12 . The composition of claim 9 , wherein component a is an anhydride-functionalized ethylene-based polymer, or an anhydride-functionalized propylene-based polymer. 13 . The composition of claim 9 , wherein component a is an anhydride-functionalized ethylene-based polymer. 14 . The composition of claim 9 , wherein, the first composition further comprises a tackifier (component c). 15 . The composition of claim 9 , wherein the first composition has a percent increase in melt viscosity at 120° C. (% Δη2 at 120° C.) from 1.0% to 25%; and where % Δη2 at 120° C.=[(η2−η1)/η1]×100, and where η2 is the melt viscosity after 2 hours at 120° C., and η1 is the melt viscosity after 1 hour at 120° C. 16 . The composition of claim 9 , wherein the first composition has a percent increase in melt viscosity at 177° C. (% Δη2 at 177° C.) from 10% to 35%; and where % Δη2 at 177° C.=[(η2−η1)/η1]×100, and where η2 is the melt viscosity after 2 hours at 177° C., and η1 is the melt viscosity after 1 hour at 177° C. 17 . The composition of claim 9 , wherein, wherein the first composition, after seven days at 22° C., 50% RH, in air atmosphere, has SAFT value from 70° C. to 135° C. 18 . A crosslinked composition formed from the first composition of claim 9 . 19 . A crosslinked composition comprising at least one of the following structure CL1, CL2, CL3 or any combination thereof: and wherein, independently, for each of CL1), CL2), CL3), each independently represents a portion of another polymer chain of the crosslinked composition; each * independently represents a portion of the remaining polymer chain bonded to the respective —CH 2 —CHZ— group noted above, where Z is the respective pendant crosslinked site noted above; X is the remaining portion of a C3 to C8 ring structure, which contains a carbon atom that is bonded to Y, or X is not present, and Y is bonded to the terminal carbon atom of a “—CH(OH)—CH 2 —O—” bridge; Y is independently a hydrocarbylene group or a heterohydro-carbylene group; each R is independently an OH group, an alkoxy group or an alkyl group. 20 . An article comprising at least one component formed from the composition of claim 8 .
leading to a crosslinking, either explicitly or inherently · CPC title
Ethene · CPC title
Reaction with unsaturated dicarboxylic acids or anhydrides thereof, e.g. maleinisation · CPC title
Hydrolysis · CPC title
Introducing metal atoms or metal-containing groups · CPC title
Related publications grouped by family.
Answers are generated from the same data shown on this page.