Proton exchange membrane with enhanced chemical stability and method of preparing thereof
US-2020343569-A1 · Oct 29, 2020 · US
US10975209B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-10975209-B2 |
| Application number | US-201916716968-A |
| Country | US |
| Kind code | B2 |
| Filing date | Dec 17, 2019 |
| Priority date | Jun 21, 2017 |
| Publication date | Apr 13, 2021 |
| Grant date | Apr 13, 2021 |
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To provide a method for producing a fluorinated polymer which enables stable production of a fluorinated polymer having a high molecular weight at a high polymerization rate with good productivity and reduced environmental burdens, a method for producing a fluorinated polymer having functional groups, and a method for producing an electrolyte membrane. A method for producing a fluorinated polymer, which comprises polymerizing a monomer mixture containing tetrafluoroethylene and a fluorinated monomer having a group convertible to a sulfonic acid group or a carboxylic acid group in a polymerization medium, wherein the polymerization medium contains as the main component a C4-10 cyclic hydrofluorocarbon. Further, a method for producing a fluorinated polymer having functional groups and a method for producing an electrolyte membrane, employing the production method.
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What is claimed is: 1. A method for producing a fluorinated polymer, which comprises polymerizing a monomer mixture containing tetrafluoroethylene and a fluorinated monomer having a group convertible to a sulfonic acid group or a carboxylic acid group in a polymerization medium, wherein the polymerization medium contains as the main component a C 4-10 cyclic hydrofluorocarbon, wherein the content of the cyclic hydrofluorocarbon is at least 50 mass % in the entire polymerization medium. 2. The method for producing a fluorinated polymer according to claim 1 , wherein the fluorinated monomer is a vinyl ether having a group convertible to a sulfonic acid group or a carboxylic acid group. 3. The method for producing a fluorinated polymer according to claim 1 , wherein the proportion of tetrafluoroethylene is from 5 to 70 mol %, and the proportion of the fluorinated monomer is from 30 to 95 mol % to the total amount of the monomer mixture. 4. The method for producing a fluorinated polymer according to claim 1 , wherein the fluorinated polymer has a TQ value of from 150 to 340° C. 5. The method for producing a fluorinated polymer according to claim 1 , wherein the fluorinated monomer contains at least one member selected from the group consisting of a monomer represented by the following formula (m1) and a monomer represented by the following formula (m2): wherein X 1 and X 2 are each independently a fluorine atom or a trifluoromethyl group, A 1 is a group convertible to a sulfonic acid group or a carboxylic acid group, p is 0 or 1, q is 0 or 1, r is an integer of from 0 to 3, s is 0 or 1, t is an integer of from 0 to 12, u is an integer of from 0 to 3, and 1≤r+u; and Q 11 is a perfluoroalkylene group which may have an etheric oxygen atom, Q 12 is a single bond or a perfluoroalkylene group which may have an etheric oxygen atom, Z 1 is a fluorine atom or a monovalent perfluoroorganic group, and v is 0 or 1. 6. The method for producing a fluorinated polymer according to claim 1 , wherein the fluorinated monomer is CF 2 ═CFOCF 2 CF(CF 3 )OCF 2 CF 2 SO 2 F, CF 2 ═CFOCF 2 CF 2 SO 2 F, CF 2 ═CFOCF 2 CF 2 CF 2 CF 2 SO 2 F or CF 2 ═CFCF 2 OCF 2 CF 2 CFSO 2 F. 7. The method for producing a fluorinated polymer according to claim 1 , wherein the fluorinated monomer is the following monomer (m2-1), (m2-2) or (m2-3): 8. The method for producing a fluorinated polymer according to claim 1 , wherein the cyclic hydrofluorocarbon has fluorine atoms in the same number or more as hydrogen atoms. 9. The method for producing a fluorinated polymer according to claim 1 , wherein the cyclic hydrofluorocarbon is 1,1,2,2,3,3,4-heptafluorocyclopentane or 1H,2H-octafluorocyclopentane. 10. A method for producing a fluorinated polymer having functional groups, which comprises producing a fluorinated polymer by the method for producing a fluorinated polymer as defined in claim 1 , and converting groups convertible to sulfonic acid groups in the fluorinated polymer to sulfonic acid groups, or converting groups convertible to carboxylic acid groups to carboxylic acid groups. 11. A method for producing an electrolyte membrane, which comprises producing a fluorinated polymer by the method for producing a fluorinated polymer as defined in claim 1 , forming a membrane by using the fluorinated polymer, and then converting groups convertible to sulfonic acid groups to sulfonic acid groups, or converting groups convertible to carboxylic acid groups to carboxylic acid groups. 12. A method for producing an electrolyte membrane, which comprises producing a fluorinated polymer having functional groups by the method for producing a fluorinated polymer having functional groups as defined in claim 10 , and forming a membrane by using the fluorinated polymer having functional groups. 13. The method for producing an electrolyte membrane according to claim 12 , wherein the fluorinated polymer having functional groups has an ion exchange capacity of from 0.5 to 2.5 meq/g dry resin. 14. A method for producing a fluorinated polymer, which comprises polymerizing a monomer mixture containing tetrafluoroethylene and a fluorinated monomer having a group convertible to a sulfonic acid group or a carboxylic acid group in a polymerization medium, wherein the polymerization medium contains as the main component a C 4-10 cyclic hydrofluorocarbon, wherein the proportion of tetrafluoroethylene is from 5 to 70 mol %, and the proportion of the fluorinated monomer is from 30 to 95 mol % to the total amount of the monomer mixture.
in the strongly acidic form · CPC title
After-treatment of fluorine-containing membranes · CPC title
using portable ion-exchange apparatus · CPC title
containing fluorine · CPC title
having only carbon, e.g. polyarylenes, polystyrenes or polybutadiene-styrenes · CPC title
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