Highly soluble tris-(2,3-epoxypropyl)-isocyanurate and method for producing same
US-12077636-B2 · Sep 3, 2024 · US
US9340642B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-9340642-B2 |
| Application number | US-99126609-A |
| Country | US |
| Kind code | B2 |
| Filing date | May 18, 2009 |
| Priority date | May 23, 2008 |
| Publication date | May 17, 2016 |
| Grant date | May 17, 2016 |
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.
This invention relates to a novel curing method of oligomers, using metal triflates, and particularly to the curing of hydroxyl terminated elastomers to achieve crosslinked polymers. The method finds particular use as an alternative cure methodology to replace isocyanate curing. There is further provided a cured and crosslinked polymer binder, which is particularly suitable and compatible for use with energetic materials.
Opening claim text (preview).
The invention claimed is: 1. A method of forming a crosslinked polyether polymer comprising the steps of forming an admixture of at least one hydroxy terminated oligomer, at least one epoxy terminated oligomer and at least one metal trifluoromethanesulfonate salt catalyst, and curing the resultant admixture at 30 to 85° C., wherein the at least one hydroxy terminated oligomer is a dihydroxy terminated oligomer of formula (ia) wherein A is a monomer repeat unit, m is the average number of monomer repeat units in the range of from 5 to 100, the at least one epoxy terminated oligomer is di-epoxy oligomer of formula (iia) wherein B is a monomer repeat unit, n is the average number of monomer repeat units in the range of from 5 to 100; wherein A and B are independently selected from monomer repeat units comprising hydrocarbyl, esters, carbonates, ethers, amides, aromatics, heterocyclic or copolymers comprising mixtures thereof and the admixture optionally comprises a further epoxy terminated oligomer of formula (iii) present in the range of from 5-10% w/w wherein D is a monomer repeat unit, wherein p is the average number of monomer repeat units in the range of 1 to 10000 and z is in the range of from 2.5 to 3, and D is independently selected from monomer repeat units comprising hydrocarbyl, esters, carbonates, ethers, amides, aromatics, heterocyclic or copolymers comprising mixtures thereof. 2. A method according to claim 1 , wherein the hydrocarbyl is a polydiene. 3. A method according to claim 1 , wherein m, n and p are in the range of from 5 to 50.
containing sulfur · CPC title
Polyalkylene oxides · CPC title
the ingredient being a polymer bonded explosive or thermic component · CPC title
containing phosphorus · CPC title
aromatic · CPC title
Related publications grouped by family.
Answers are generated from the same data shown on this page.