Ion exchange membrane
US-9745433-B2 · Aug 29, 2017 · US
US10150113B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-10150113-B2 |
| Application number | US-201615135851-A |
| Country | US |
| Kind code | B2 |
| Filing date | Apr 22, 2016 |
| Priority date | Dec 28, 2015 |
| Publication date | Dec 11, 2018 |
| Grant date | Dec 11, 2018 |
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A polymer and a method for preparing the same are provided. The polymer includes a first repeat unit and a second repeat unit. In particular, the first repeat unit is and, the second repeat unit is wherein R + is A − is F − , Cl − , Br − , I − , OH − , HCO 3 − , HSO 4 − , SbF 6 − , BF 4 − , H 2 PO 4 − , H 2 PO 3 − , or H 2 PO 2 − ; X is i and j are independently 0, or an integer from 1 to 4; Y is —O—, —S—, —CH 2 —, or —NH—; R 1 is independently C 1-8 alkyl group; and, R 2 and R 3 are hydrogen, or independently C 1-8 alkyl group.
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What is claimed is: 1. A polymer, comprising a first repeat unit and a second repeat unit, wherein the first repeat unit is the second repeat unit is wherein R + is A − is F − , Cl − , Br − , I − , OH − , HCO 3 − , HSO 4 − , SbF 6 − , BF 4 − , H 2 PO 4 − , H 2 PO 3 − , or H 2 PO 2 − ; X is i and j is independently an integer from 1 to 6, Y is —O—, —S—, —CH 2 —, or —NH—; R 1 is independently C 1-8 alkyl group; and, R 2 and R 3 are independently hydrogen, or C 1-8 alkyl group. 2. The polymer as claimed in claim 1 , wherein the ratio between the first repeat unit and the second repeat unit is between 1:99 and 99:1. 3. The polymer as claimed in claim 1 , wherein R 1 is methyl, ethyl, propyl, isopropyl, n-butyl, sec-butyl, isobutyl, tert-butyl, pentyl, hexyl, cyclohexyl, cyclopentyl, heptyl, or octyl. 4. The polymer as claimed in claim 1 , wherein R 2 and R 3 are independently hydrogen, methyl, ethyl, propyl, isopropyl, n-butyl, sec-butyl, isobutyl, tert-butyl, pentyl, hexyl, cyclohexyl, cyclopentyl, heptyl, or octyl. 5. The polymer as claimed in claim 1 , wherein the first repeat unit is wherein R + is A − is F − , Cl − , Br − , I − , OH − , HCO 3 − , HSO 4 − , SbF 6 − , BF 4 − , H 2 PO 4 − , H 2 PO 3 − , or H 2 PO 2 − ; i and j is independently an integer from 1 to 6; and, R 2 and R 3 are independently hydrogen, or C 1-8 alkyl group. 6. The polymer as claimed in claim 1 , wherein the first repeat unit is wherein A − is F − , Cl − , Br − , I − , OH − , HCO 3 − , HSO 4 − , SbF 6 − , BF 4 − , H 2 PO 4 − , H 2 PO 3 − , or H 2 PO 2 − ; X is i and j is independently an integer from 1 to 6, Y is —O—, —S—, —CH 2 —, or —NH—; and, R 2 and R 3 are independently hydrogen, or C 1-8 alkyl group. 7. The polymer as claimed in claim 1 , wherein the second repeat unit is 8. The polymer as claimed in claim 1 , wherein the polymer further comprising a third repeat unit, wherein the third repeat unit is 9. The polymer as claimed in claim 8 , wherein the ratio between the third repeat unit and the sum of the first repeat unit and the second repeat unit is between 0.1:100 and 5:100. 10. A method for preparing the polymer as claimed in claim 1 , comprising: subjecting a composition to a polymerization, wherein the composition comprises a first monomer having a structure of Formula (I), and a second monomer having a structure of Formula (II) wherein R + is A − is F − , Cl − , Br − , I − , OH − , HCO 3 − , HSO 4 − , SbF 6 − , BF 4 − , H 2 PO 4 − , H 2 PO 3 − , or H 2 PO 2 − ; X is i and j is independently an integer from 1 to 6, Y is —O—, —S—, —CH 2 —, or —NH—; R 1 is independently C 1-8 alkyl group; and, R 2 and R 3 are independently hydrogen, or C 1-8 alkyl group. 11. The method as claimed in claim 10 , wherein the molar ratio between the first monomer and the second monomer is between 1:99 and 99:1. 12. The method as claimed in claim 10 , wherein R 1 is methyl, ethyl, propyl, isopropyl, n-butyl, sec-butyl, isobutyl, tert-butyl, pentyl, hexyl, cyclohexyl, cyclopentyl, heptyl, or octyl. 13. The method as claimed in claim 10 , wherein R 2 and R 3 are independently hydrogen, methyl, ethyl, propyl, isopropyl, n-butyl, sec-butyl, isobutyl, tert-butyl, pentyl, hexyl, cyclohexyl, cyclopentyl, heptyl, or octyl. 14. The method as claimed in claim 10 , wherein the first monomer is wherein R + is A − is F − , Cl − , Br − , I − , OH − , HCO 3 − , HSO 4 − , SbF 6 − , BF 4 − , H 2 PO 4 − , H 2 PO 3 − , or H 2 PO 2 − ; i and j is independently an integer from 1 to 6; and, R 2 and R 3 are independently hydrogen, or C 1-8 alkyl group. 15. The method as claimed in claim 10 , wherein the first monomer is wherein A − is F − , Cl − , Br − , I − , OH − , HCO 3 − , HSO 4 − , SbF 6 − , BF 4 − , H 2 PO 4 − , H 2 PO 3 − , or H 2 PO 2 − ; X is i and j is independently an integer from 1 to 6, Y is —O—, —S—, —CH 2 —, or —NH—; and, R 2 and R 3 are independently hydrogen, or C 1-8 alkyl group. 16. The method as claimed in claim 10 , wherein the second monomer is 17. The method as claimed in claim 10 , wherein the composition further comprises a third monomer, wherein the third monomer is 18. The method as claimed in claim 17 , wherein the molar ratio between the third monomer and the sum of the first monomer and the second monomer is between 0.1:100 and 5:100.
having one carbon-to-carbon double bond · CPC title
Polymers obtained by reactions only involving carbon-to-carbon unsaturated bonds, not provided for in a single one of groups B01D71/26-B01D71/42 · CPC title
of carbocyclic compounds containing one or more carbon-to-carbon double bonds in the ring · CPC title
Cross-linked structures · CPC title
Ring opening metathesis polymerisation [ROMP] · CPC title
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