US2014155502A1PendingUtilityA1
Functionalized main chain polymers
Est. expiryNov 22, 2021(expired)· nominal 20-yr term from priority
Inventors:Thomas Häring
B01D 71/5221B01D 67/0093Y02E60/50H01M 8/1034C08J 2381/06H01M 8/1027C08G 75/23B01J 41/12B01D 71/82H01M 2008/1095C08L 2312/00H01M 8/0289B01J 47/12B01D 71/80B01D 71/68C08L 71/00H01M 8/1039H01M 8/1032H01M 2300/0082C08J 5/2256C08G 2650/20C08J 2371/00C08G 65/48B01D 2323/30C08L 81/06H01M 2300/0091B01J 39/19C08J 5/2275C08G 2650/02B01J 39/185
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Claims
Abstract
A non crosslinked, covalently crosslinked and/or conically crosslinked polymer, having repeating units of the general formula (1) —K—R— (1) In which K is a bond, oxygen, sulfur, the radical R is a divalent radical of an aromatic or heteroaromatic compound.
Claims
exact text as granted — not AI-modifiedI claim:
1 . A non-crosslinked, covalently cross-linked and/or ionically cross-linked polymer, having repeating units of the general formula (1)
—K—R— (1)
in which K is a bond, oxygen, sulpur,
and the radical R is a divalent radical of an aromatic or heteroaromatic compound comprising at least in part bridges of the general formula:
which joins at least two radicals to one another, Y being a group having 1 to 40 carbon atoms, preferably, an alkyl or cycloalkyl group, or an alkylated aryl group, Z being (i) a group including a hydroxyl, (ii) a group having a molecular weight greater than 20 g/mol, composed of optional components H, C, O, N, S, P and halogen atoms, or (iii) a group of the general formula:
and m being an integer greater than or equal to 2.
2 . The polymer of claim 1 , wherein the polymer is doped with acid.
3 . The polymer of claim 2 , wherein the acid comprises phosphoric acid.
4 . The polymer of claim 1 , further comprising a designating sulfinate group of the general formula:
5 . The polymer of claim 4 , wherein the sulfinate group is reacted with a compound of the general formula:
YL m where L is a leaving group and n is an integer greater than or equal to 2.
6 . The polymer of claim 4 , wherein the polymer is formed in a mixture comprising at least one precursor polymer having the designated sulfinate group,
7 . The polymer of claim 6 , wherein the precursor polymer is dissolved in a polar-aprotic solvent selected from the group of consisting of N,N-dimethylformamide, N,N-dimethylactamide, N-methylpyrrolidone, dimethyl sulfoxide or dimethyl sulfolane.
8 . The polymer of claim 6 , wherein the solution is reacted with a halogen compound, under stirring.
9 . The polymer of claim 4 , wherein the polymer is formed in solution in a process in which the polymer solution is spread as a film on to a substrate and the solvent is evaporated at an elevated temperature of higher than 25° C.
10 . The polymer of claim 9 , wherein the process is carried out under a pressure of 1000 mbar.
11 . The polymer of claim 4 , wherein the polymer is formed in a process in which the polymer is first treated with acid and then with deionized water.
12 . The polymer of claim 11 , wherein the polymer is treated with an aqueous alkali prior to being treated with acid.Cited by (0)
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