Co-ABPBI membranes and process for the preparation thereof

Patent metadata

Field	Value
Publication number	US-10023705-B2
Application number	US-201414915346-A
Country	US
Kind code	B2
Filing date	Sep 1, 2014
Priority date	Aug 30, 2013
Publication date	Jul 17, 2018
Grant date	Jul 17, 2018

Abstract

Disclosed herein is co-ABPBI membranes comprising co-ABPBI of formula (I), Invention discloses a sol gel process for the synthesis of membranes comprising co-ABPBI of formula (I).

First claim

We claim:

1. A process for the preparation of a Co-ABPBI membrane comprising the steps of:
a. heating polyphosphoric acid (PPA) with stirring at 100-140° C. under constant flow of nitrogen followed by addition of 50 to 99 mol. % of 3,4-diaminobenzoic acid (DABA) and 1 to 50 mol. % of dicarboxylic acid selected from formula IIIa-e to obtain a reaction mixture; wherein formula IIIa-e are shown below:
HOOC—(C k H m X n )—COOH   Formula-IIIa

where, k=1-30 containing fused aromatic ring (containing phenyl, pyridine, pyrazine, furan, quinoline, thiophene or appropriate aromatic rings containing hetero-aromatic fused ring systems) substituted with alkyl, aryl, arylene, alkylene, arylene-ether or heterocyclic groups as straight chain, branched, cyclic, aromatic or combination thereof; X═O, N, S, halogen or combination thereof, n=0-10 and m=appropriate numbers of hydrogen; or

wherein; R 1 , R 2 ═H, OH, O-alkyl, CH 3 , CF 3 , F, Cl, Br, I, NO 2 or C 1-15 containing alkyl, aryl, aromatic ring, arylene, alkylene, arylene-ether or heterocyclic ring selected from group consisting of pyridine, pyrazine, furan, quinoline, thiopene groups; or

where; R 1 , R 2 , R 3 , R 4 ═H, OH, O-alkyl, CH 3 , CF 3 , F, Cl, Br, I, NO 2 or C 1-15 containing alkyl, aryl, aromatic ring, arylene, alkylene, arylene-ether or heterocyclic ring selected from group pyridine, pyrazine, furan, quinoline, thiopene groups and X is selected from the group consisting of —CH 2 —, —O—, —SO 2 —, —C(CH 3 ) 2 —, —C(CF 3 ) 2 —, —C(Ph) 2 -, —CH 3 C(Ph)-, —CH 3 C(isopropyl)-, —CH 3 C(t-butyl)-, —CH 3 C(n-propyl)-, —CH 3 C(ethyl)- or C 1-15 containing alkyl or aryl groups

where; R 1 , R 2 , R 3 , R 4 , R 5 , R 6 , R 7 , R 8 ═H, OH, O-alkyl, CH 3 , CF 3 , F, Cl, Br, I, NO 2 or C 1-15 containing alkyl, aryl, aromatic ring, arylene, alkylene, arylene-ether or heterocyclic ring such as pyridine, pyrazine, furan, quinoline, thiopene groups

where; R 1 , R 2 , R 3 , R 4 ═H, OH, O-alkyl, CH 3 , CF 3 , F, Cl, Br, I, NO 2 or C 1-15 containing alkyl, aryl, aromatic ring, arylene, alkylene, arylene-ether or heterocyclic ring selected from group consisting of pyridine, pyrazine, furan, quinoline, thiopene groups;

b. increasing the temperature of the reaction mixture obtained in step (a) to 170° C. and maintaining it for 10 min to 10 hours;
c. lowering the temperature of reaction mixture of step (b) to 140° C. and adding 1 to 50 mol. % tetraamine selected from formula IIa-f, while maintaining the temperature for 10 min to 5 hours; wherein formula IIa-f are shown below:

wherein, R 1 , R 2 is selected form a group consisting of H, CH 3 , CF 3 , F, Cl, Br, I, NO 2 or C 1-24 containing alkyl or aryl groups; or

wherein, R 1 , R 2 , R 3 , R 4 is selected form a group consisting of H, CH 3 , CF 3 , F, Cl, Br, I, NO 2 or C 1-24 alkyl or aryl groups; or

wherein, R 1 , R 2 , R 3 , R 4 is selected form a group consisting of H, CH 3 , CF 3 , F, Cl, Br, I, NO 2 or C 1-24 alkyl or aryl groups; or

wherein, R 1 , R 2 , R 3 , R 4 is selected form a group consisting of H, CH 3 , CF 3 , F, Cl, Br, I, NO 2 or C 1-24 alkyl or aryl groups; or

wherein, R 1 , R 2 , R 3 , R 4 is selected form a group consisting of H, CH 3 , CF 3 , F, Br, I, NO 2 or C 1-24 alkyl or aryl groups and X is selected from the group consisting of —CH 2 —, —O—, —SO 2 —, —C(CH 3 ) 2 —, —C(CF 3 ) 2 —, —C(Ph) 2 -, —CH 3 C(Ph)-, —CH 3 C(isopropyl)-, —CH 3 C(t-butyl)-, —CH 3 C(n-propyl)-, —CH 3 C(ethyl)- or any other C 1-24 containing alkyl or aryl groups; or

d. increasing the temperature of the reaction mixture of step (c) to 170° C., maintaining it for 10 min to 5 h, followed by raising the temperature to 190-210° C. and maintaining it for 10 min to 14 h to obtain the co-ABPBI of Formula-I,

wherein m and n are repeat units; R is tetraamine monomer selected from compounds of Formula IIa-f and FAR is fused aromatic ring derived from dicarboxylic acid selected from compounds of Formula IIIa-e or its positional isomers, salts or esters;
e. adding water and phosphoric acid to the reaction mixture in the ratio 0:100 to 100:0 to the reaction mixture of co-ABPBI of formula-I followed by stirring for 10 min-10 h;
f. degassing the solution of step (e) for 5-60 min to remove entrapped air and casting it on a support to obtain a membrane;
g. keeping the membrane obtained in step (f) above in humidity chamber at 20-95% RH, −10-60° C. and 1-48 h for hydrolysis of PPA to obtain the Co-ABPBI membrane; and
h. optionally vacuum drying the Co-ABPBI membrane obtained in step (g) at 40-150° C.

2. The process of claim 1 , wherein in step (f) the support is selected from glass plate, glass fabric, polytetrafluoroethylene paper, and polyetheretherketone (PEEK).

Assignees

• Council Scient Ind Res

Inventors

• Kharul Ulhas Kanhaiyalal
• Sreekumar Kurungot
• Chaudhari Harshal Dilip
• Ghodake Vinaya Bhagwat

Classifications

• H01G11/52

  Separators · CPC title

• B01D53/228 Primary

  characterised by specific membranes · CPC title

• H01M8/1081

  starting from solutions, dispersions or slurries exclusively of polymers · CPC title

• H01M8/1074

  Sol-gel processes · CPC title

• H01M8/1072

  by chemical reactions, e.g. in situ polymerisation or in situ crosslinking · CPC title