Epoxy resin formulations and processes for producing aerospace-grade composites via low temperature, isothermal infusion
US-2024376278-A1 · Nov 14, 2024 · US
US9963563B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-9963563-B2 |
| Application number | US-201715724028-A |
| Country | US |
| Kind code | B2 |
| Filing date | Oct 3, 2017 |
| Priority date | May 22, 2007 |
| Publication date | May 8, 2018 |
| Grant date | May 8, 2018 |
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The embodiments of the present disclosure present systems and methods for the reversible solubilization of (aryl ether ketones) (PAEKs). A thioacetalization process is employed to modify the PAEKs into poly (aryl ether thioacetals) which, unlike PAEKs, are substantially soluble in common solvents. This modification allowing selected analysis techniques to be more easily performed on PAEKs, such as gel permeation chromatography. The thioacetalization may be reversed through a deprotection reaction to recover the original PAEK without substantial degradation, allowing for non-destructive characterization of the PAEK. Advantageously, the thioacetalization process is generally applicable to a broad range of PAEKs, unlike presently known methods of solubilizing PAEKs. Solubilization of PAEKs further expands the utility of the PAEKs, opening up additional routes to chemical modification of PAEKs, as well as allowing for the possibility of processing PAEKs from solution.
Opening claim text (preview).
The invention claimed is: 1. A method of forming a soluble derivative of a poly (aryl ether ketone) (“PAEK”), comprising: mixing a starting poly (aryl ether ketone) (PAEK) polymer with a solvent and an acid, said solvent being selected from a group consisting of diethylether, tetrahydrofuran (THF), dioxin, and chlorinated solvents; and reacting the PAEK mixture with a Lewis acid and a thiol compound in amounts effective to form a poly (aryl ether thioacetal) compound which comprises at least one thioacetal group; wherein the Lewis acid is boron trifluoride diethyl etherate (BF 3 Et 2 O), the thiol compound is 1,2 ethanedithiol or 1,3-propanedithiol, and the starting PAEK is selected from: poly (ether ketone) (“PEK”), poly (ether ether ketone) (“PEEK”), poly (ether ketone ketone) (“PEKK”), and poly (ether ketone ether ketone ketone) (“PEKEKK”). 2. The method of claim 1 , wherein the chlorinated solvent is selected from at least one of dichloromethane (DCM), trichloromethane (chloroform), dichloroethane, and dichlorobenzene. 3. The method of claim 1 , wherein the acid being mixed with the starting PAEK is a non-sulfonating acid. 4. The method of claim 1 , wherein the acid being mixed with the starting PAEK is trifluoroacetic acid. 5. The method of claim 1 , wherein the starting PAEK is PEEK and the poly (aryl ether thioacetal) compound comprises the following recurring unit (a) or (b): 6. The method of claim 1 , wherein the starting PAEK is PEK and the poly (aryl ether thioacetal) compound comprises the following recurring unit (c) or (d): 7. The method of claim 1 , wherein the starting PAEK is PEKK, the thiol compound is 1,2-ethanedithiol, and the poly (aryl ether thioacetal) compound comprises the following recurring units (e) and (f): 8. The method of claim 1 , wherein the starting PAEK is PEKK, the thiol compound is 1,3-propanedithiol, and the poly (aryl ether thioacetal) compound comprises the following recurring units (g) and (h): 9. The method of claim 1 , wherein the starting PAEK is PEKEKK, the thiol compound is 1,2-ethanedithiol, and the poly (aryl ether thioacetal) compound comprises the following recurring unit (i): 10. The method of claim 1 , wherein the starting PAEK is PEKEKK, the thiol compound is 1,3-propanedithiol, and the poly (aryl ether thioacetal) compound comprises the following recurring unit (j):
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