Latent epoxy resin formulations for liquid impregnation processes for production of fibre-reinforced composites
US-10155840-B2 · Dec 18, 2018 · US
US10035874B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-10035874-B2 |
| Application number | US-201514797378-A |
| Country | US |
| Kind code | B2 |
| Filing date | Jul 13, 2015 |
| Priority date | Jul 16, 2014 |
| Publication date | Jul 31, 2018 |
| Grant date | Jul 31, 2018 |
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An epoxide based composition that can be cured at a temperature of less than about 70 C is disclosed. The composition is a liquid at ambient conditions and, therefore, can be used to rehabilitate the interior surfaces of pipelines. The epoxide-based composition comprises at least one epoxide component (component A) and at least one curing agent component (component B) wherein (A) the epoxide component comprises a phenyl glycidyl ether polyepoxide; and (B) the curing agent component comprises a mixture of two salt compounds formed, respectively, from an N-alkanol piperidine and a carboxylic acid bearing 7-12 carbon atoms, and N-cyclohexyl-N,N-dialkyl amine and a carboxylic acid bearing 7-12 carbon atoms.
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We claim: 1. An epoxide-based composition, comprising (A) an epoxide component comprising at least one phenyl glycidyl ether polyepoxide having at least two epoxide group of oxirane structure in the molecule; and (B) a curing agent component comprising a mixture of (i) a first salt comprising a salt of an N-alkanol piperidine and at least one carboxylic acid bearing 6-12 carbon atoms and (ii) a second salt consisting of a salt of N-cyclohexyl-N,N-dialkyl amine and a monovalent organic carboxylic acid bearing 6-12 carbon atoms; wherein the salt of N-alkanol piperidine in the mixture ranges from 20-80 wt %. 2. The composition of claim 1 wherein the amount of the curing agent of component (B) is from about 1 to about 50 wt parts per 100 wt parts of the epoxide component (A). 3. The epoxide-based composition according to claim 1 , wherein the epoxide component (A) further comprises an epoxide compound other than a phenyl glycidyl ether polyepoxide. 4. The epoxide-based composition according to claim 3 , wherein the epoxide compound is at least one compound selected from the group consisting of glycidyl ethers, glycidyl esters and glycidyl amines. 5. The epoxide-based composition according to claim 1 , wherein the N-alkanol piperidine is selected from the group consisting of N-piperidine ethanol and N-piperidine propanol and the N-cyclohexyl-N,N-dialkyl amine is selected from the group consisting of N-cyclohexyl-N,N-dimethylamine and N-cyclohexyl-N,N-dipropylamine. 6. The epoxide-based composition according to claim 1 further comprising at least one diluent selected from the group consisting of mono glycidyl ethers. 7. The epoxide-based composition according to claim 6 wherein the diluents comprises at least one member selected from the group consisting of butyl glycidyl ether, phenyl glycidyl ether, and dodecyl glycidyl ether. 8. The epoxide-based composition according to claim 1 further comprising at least one accelerator selected from the group consisting of imidazoles. 9. The epoxide-based composition of claim 8 wherein the imidzoles comprise at least one member selected from the group consisting of 1-methylimidazole, and 2-methylimidazole. 10. The epoxide-based composition according to claim 1 further comprising at least one accelerator selected from the group consisting of phenolic tertiary amine derivatives tris(dimethylaminomethyl)phenol, and dimethylaminomethylphenol. 11. A method for treating a substrate comprising applying the epoxide-based composition of claim 1 onto a substrate, heating the substrate to a temperature of less than about 80° C. and curing the composition. 12. The method of claim 11 wherein the substrate comprises an interior surface of a conduit or pipe. 13. The method of claim 12 wherein the surface comprises a fibrous material within the conduit or pipe. 14. A treated substrate made in accordance with the method of claim 11 . 15. The method of claim 12 wherein the conduit or pipe is cured in place without digging or removing the pipe. 16. The method of claim 15 wherein treatment is applied using cured in place pipe (CIPP) technology. 17. The epoxide-based composition according to claim 1 , further comprising at least one hindered polyether amine selected from the group consisting of polyoxypropylenediamine having a molecular weight of about 230, polyoxypropylenediamine having a molecular weight of about 430, and polyoxypropylenetriamine having a molecular weight of about 400.
having one nitrogen atom in the ring · CPC title
aliphatic · CPC title
from inside the pipe ({F16L55/1612 takes precedence;} specially adapted for bends, branch units, branching pipes, or the like F16L55/179) · CPC title
Diluents or solvents · CPC title
aromatic · CPC title
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