POLYMER LAYERED HOLLOW FIBER MEMBRANE BASED ON POLY(2,5-BENZIMIDAZOLE), COPOLYMERS AND SUBSTITUTED POLYBENZIMIDAZOLE

Abstract

The present invention relates to a polymer layered hollow fiber membrane based on poly(2,5-benzimidazole) (ABPBI), ABPBI copolymers and substituted polybenzimidazole (PBI) and a process for preparation thereof.

Claims

1. A polymer layered fiber membrane comprising one to three polymers layers wherein i. the polymer for a first layer is selected from the group consisting of poly(2,5-benzimidazole)(ABPBI), or poly(2,5-benzimidazole) (ABPBI) copolymers, or substituted polybenzimidazole (PBI) or blends thereof; ii. the polymer for a second layer is selected from the group consisting of polyetherimide, polyamide, polyacrylonitrile, polysulfones, polyether sulfone, polyvinylidene fluoride, polyimide, polyphenylene oxide, cellulose acetates alone or in combinations thereof; and iii. the polymer for a third layer is selected from the group consisting of silicone rubber, ethyl cellulose, poly(phyneleneoxide), poly(tetramethyl bisphenol-A-iso-terephthalate) or poly[1-(trimethylsilyl)-1-propyne; wherein one layer of said membrane is polymer of first layer; wherein said membrane is hollow fiber and substantially non-porous.

2. The polymer membrane as claimed in claim 1, wherein said poly(2,5-benzimidazole) (ABPBI) copolymers is selected from the group consisting of ABPBI-co-PBI, ABPBI-co-substituted PBI or ABPBI-co-naphthalene dicarboxylic acid based PBIs.

3. The polymer membrane as claimed in claim 1, wherein said substituted polybenzimidazole is selected from the group consisting of tert-butyl substituted polybenzimidazole, hexafluoroisopropylidene substituted polybenzimidazole, dimethylsubstituted polybenzimidazole or di-tert-butylbenzyl substituted polybenzimidazole.

4. The polymer membrane as claimed in claim 1, wherein said membrane is useful for separation or transport of solvents, solutes, acids, bases, chemicals and gases in selective manner.

5. A process for the preparation of polymer membrane as claimed in claim 1, comprising the steps of: a) preparing a first dope solution by dissolving the first polymer in a solvent or solvent mixtures followed by stirring the mixture at temperature in the range of 60 to 120° C. for the period in the range of 1 to 72 h; b) preparing a second dope solution by dissolving second polymer in solvent followed by stirring the reaction mixture at temperature in the range of 60 to 90° C. for the period in the range of 1 to 72 h; c) subjecting the first dope solution of step (a) and second dope solution of step (b) to dry-jet/wet spinning process to afford polymer layered hollow fiber membrane; and d) coating the membrane of step (c) with a third polymer to afford three layered membrane.

6. The process as claimed in claim 5, wherein said solvent is selected from group consisting of pyridine, dimethyl sulfoxide, N,N-dimethyl formamide, N,N-dimethyl acetamide, N-Methyl-2-pyrrolidone, methane sulphonic acid, sulphuric acid, phosphoric acid, polyphosphoric acid, formic acid, acetone, tetrahydrofuran or mixture thereof.

7. The process as claimed in claim 5, wherein said first polymer is selected from the group consisting of poly(2,5-benzimidazole), or poly(2,5-benzimidazole) copolymers, or substituted polybenzimidazole; wherein said substituted polybenzimidazole are selected from tert-butyl substituted polybenzimidazole, hexafluoroisopropylidene substituted polybenzimidazole, dimethylsubstituted polybenzimidazole, di-tert-butylbenzyl substituted polybenzimidazole.

8. The process as claimed in claim 5, wherein said second polymer is selected from the group consisting of polyetherimide, polyamide, polyacrylonitrile, polysulfones, polyether sulfone, polyvinylidene fluoride, polyimide, polyphenylene oxide, cellulose acetates either alone or combination thereof.

9. The process as claimed in claim 5, wherein said third polymer is selected from the group consisting of silicone rubber, ethyl cellulose, poly(phyneleneoxide), poly(tetramethyl bisphenol-A-iso-terephthalate) or poly[1-(trimethylsilyl)-1-propyne.

Description

BRIEF DESCRIPTION OF THE DRAWINGS

[0044] FIG. 1: Optical image of a neat ABPBI based hollow fiber membrane.

[0045] FIG. 2: Optical image of dual layer ABPBI-PAN fiber; (a)—ABPBI layer and (b)—PAN layer

[0046] FIG. 3: Optical image of dual layer PBI-BuI-PSF fiber; (a)—PBI-BuI layer and (b)—PSF layer.

DETAILED DESCRIPTION OF THE INVENTION

[0047] The term “substantially non-porous” states that “a membrane that is substantially non-porous is a membrane capable of being used for chemodialysis, forward osmosis, pervaporation, gas separation, nanofiltration, ultrafiltration or reverse osmosis.”

[0048] The present invention provides a polymer layered hollow fiber membrane based on poly(2,5-benzimidazole) (ABPBI), poly(2,5-benzimidazole) (ABPBI) copolymers and substituted polybenzimidazole (PBI) and a process for the preparation thereof.

[0049] The present invention provides a substantially non-porous polymer layered hollow fiber membrane comprising one or more polymers layers, wherein [0050] i. the polymer for a first layer is selected from the group consisting of poly(2,5-benzimidazole) (ABPBI), poly(2,5-benzimidazole) (ABPBI) copolymers, or substituted polybenzimidazole (PBI) or blends thereof; [0051] ii. the polymer for a second layer is selected from the group consisting of polyetherimide (PEI), polyamide (PA), polyacrylonitrile (PAN), polysulfones (PS), polyether sulfone (PES), polyvinylidene fluoride (PVDF), polyimide (PI), polyphenylene oxide (PPO), cellulose acetates (CA) alone or in combinations thereof; [0052] iii. the polymer for third layer is selected from the group consisting of silicone rubber, ethyl cellulose, poly(phyneleneoxide), poly(tetramethyl bisphenol-A-iso-terephthalate) or poly[1-(trimethylsilyl)-1-propyne (PTMSP);

[0053] with the proviso that one layer of the membrane is polymer of first layer and when the membrane wherein the polymer layered hollow fiber membrane is substantially non-porous.

[0054] In an embodiment of the present invention, poly(2,5-benzimidazole) (ABPBI) copolymer is selected from the group consisting of ABPBI-co-PBI, ABPBI-co-substituted PBI or ABPBI-co-naphthalene dicarboxylic acid based PBIs.

[0055] The single layered membrane further comprises blends of poly(2,5-benzimidazole) (ABPBI) or its copolymer or their blends with substituted polybenzimidazole (PBI).

[0056] The thickness of the layer of single, double or three layer membrane is in the range of 0.05 to 300 μm.

[0057] The non-porous polymer layered hollow fiber membrane based on poly(2,5-benzimidazole) (ABPBI), ABPBI copolymers and substituted polybenzimidazole (PBI) further comprising the polymer of third layer.

[0058] The polymer for third layer is selected from Silicone rubber, ethyl cellulose, poly(phyneleneoxide), poly(tetramethyl bisphenol-A-iso-terephthalate) or poly[1-(trimethylsilyl)-1-propyne (PTMSP).

[0059] The substituted polybenzimidazole is selected from tert-butyl substituted polybenzimidazole, hexafluoroisopropylidene substituted polybenzimidazole, dimethylsubstituted polybenzimidazole, di-tert-butylbenzyl substituted polybenzimidazole

[0060] The structure of poly(2,5-benzimidazole) (ABPBI), is disclosed in the reference WO-2011104602.

[0061] The structure of tert-butyl substituted polybenzimidazole is disclosed in the reference J. Membr. Sci. 286 (2006) 161.

[0062] The structure of hexafluoroisopropylidene substituted polybenzimidazole is disclosed in the reference J. Membr. Sci. 286 (2006) 161.

[0063] The structure of dimethylsubstituted polybenzimidazole is disclosed in the reference Eur. Polym. J. 45 (2009) 3363.

[0064] The structure of di-tert-butylbenzyl substituted polybenzimidazole is disclosed in the reference Eur. Polym. J. 45 (2009) 3363.

[0065] The present invention provides a process for the preparation of the substantially non-porous polymer layered hollow fiber membrane comprising the steps of: [0066] a) preparing a first dope solution by dissolving the first polymer in a solvent or solvent mixtures followed by stirring the mixture at temperature in the range of 60 to 120° C. for the period in the range of 1 to 72 h; [0067] b) preparing a second dope solution by dissolving second polymer in solvent followed by stirring the reaction mixture at temperature in the range of 60 to 90° C. for the period in the range of 1 to 72 h; [0068] c) subjecting the first dope solution of step (a) and second dope solution of step (b) to dry-jet/wet spinning process to afford one or two layered hollow fiber membrane; and [0069] d) coating the membrane of step (c) with a third polymer to afford three layered membrane.

[0070] The solvent is selected from the group consisting of pyridine, dimethyl sulfoxide, N,N-dimethyl formamide, N,N-dimethyl acetamide, N-Methyl-2-pyrrolidone, methane sulphonic acid, sulphuric acid, phosphoric acid, polyphosphoric acid, formic acid, acetone, tetrahydrofuran or mixture thereof.

[0071] The first polymer is selected from the group consisting of poly(2,5-benzimidazole) (ABPBI), or poly(2,5-benzimidazole) (ABPBI) copolymers, or substituted polybenzimidazole (PBI) or blends thereof.

[0072] The second polymer is selected from the group consisting of polyetherimide, polyamide, polyacrylonitrile, polysulfones, polyether sulfone, polyvinylidene fluoride, polyimide, polyphenylene oxide, cellulose acetates alone or in combinations thereof.

[0073] The third polymer is selected from the group consisting of Silicone rubber, ethyl cellulose, poly(phyneleneoxide), poly(tetramethyl bisphenol-A-iso-terephthalate) or poly[1-(trimethylsilyl)-1-propyne (PTMSP).

[0074] The present invention further provides use of the polymer layered hollow fiber membrane for separation or transport of solvents, solutes, acids, bases, chemicals and gases in selective manner.

[0075] The present invention further provides the hollow fiber membrane modules of having different shapes. In the present invention, shell and tube type and U-shaped membranes modules are used for transport analysis. The transport analysis is carried out by flux studies. Different solvents, solutes, acids, bases, chemicals and gases are used for transport analysis.

[0076] The shell and tube type membrane module is prepared by potting the hollow fiber membrane by using two-component epoxy glue. When the shell and tube type membrane module is used for transport analysis, feed solution is passed through shell side and stripping solution is passed through tube side or vice versa.

[0077] The U-shaped membrane module is prepared by potting the hollow fiber membrane by using two-component epoxy glue. When the U-shaped membrane module is used for transport analysis, module is dipped in the feed solution container (feed side) and the stripping solution is passed through tube side (strip side) or vice versa.

[0078] The U-shaped membrane module is used for the transport analysis of acid. In the present invention, inventor studies the transport analysis by dipping U-shaped module into the acid container (feed side) and water was circulated from the tube side (strip side). The transport of different acids viz., HNO.sub.3, H.sub.2SO.sub.4 or H.sub.3PO.sub.4 was evaluated at different concentrations: 0.5 M, 1 M, 1.5 M and 2M. The flux of acid (amount transported from feed side to tube side) transported on the tube side is monitored by sampling and titration. The flux data for single layer membrane is given in Table 1.

TABLE-US-00001 TABLE 1 Flux of inorganic acids for single layer membrane Flux of acid (g .Math. m.sup.−2 .Math. h.sup.−1) At feed At feed At feed At feed concentra- concentra- concentra- concentra- Acid tion = 0.5M tion = 1.0M tion = 1.5M tion = 2.0M HNO.sub.3 87.0 178.2 231.5 524.5 H.sub.2SO.sub.4 62.1 64.9 128.9 246.9 H.sub.3PO.sub.4 24.1 43.1 49.5 71.3

[0079] The transport of organic acids from the feed side to the tube side (strip side) of the membrane module was evaluated using acetic acid, glycolic acid, and lactic acid. The feed concentration for individual acid was varied from 0.5 M, 1.5M and 2M and the acid transported to the tube side was evaluated by titration. The flux data is given in Table 2.

TABLE-US-00002 TABLE 2 Flux of organic acids for single layer membrane Flux of acid (g .Math. m.sup.−2 .Math. h.sup.−) At feed At feed At feed concentration = concentration = concentration = Acid 0.5M 1.5M 2M Acetic acid 36.5 84.5 258.6 Glycolic acid 36.1 77.2 188.7 Lactic acid 21.11 64.9 107.8

[0080] The shell and tube type membrane module was used for gas permeation analysis. The individual gas (He, N.sub.2, CO.sub.2 or CH.sub.4) was pressurized to the shell side of the membrane at either 50, 60 or 70 psi. The permeation analysis is as given in Table 3

TABLE-US-00003 TABLE 3 Gas permeation data of PEI and PBI-BuI dual-layer hollow fiber membrane coated with silicon rubber Feed P He N.sub.2 CO.sub.2 CH.sub.4 Selectivity Selectivity Selectivity (psi) (GPU) (GPU) (GPU) (GPU) (He/N.sub.2) (CO.sub.2/N.sub.2) (CO.sub.2/CH.sub.4) 50 1.04 0.02 0.15 0.02 49.14 7.09 6.89 60 1.15 0.02 0.18 0.02 49.11 7.67 8.25 70 1.21 0.03 0.16 0.03 46.52 6.22 5.78

EXAMPLES

[0081] Following examples are given by way of illustration therefore should not be construed to limit the scope of the invention.

Example 1: Preparation of ABPBI and Copolymers

Example 1a: Preparation of ABPBI

[0082] The ABPBI was synthesized in a reactor equipped with an overhead stirrer. It was charged with polyphosphoric acid (PPA, 2100 g) and heated at 170° C. A 70 g of 3,4-diaminobenzoic acid (DABA) was added and heated for 1 h. The temperature was raised to 200° C., maintained for 1 h while stirring. The polymer was precipitated in water, cut into pieces, crushed, and agitated in water till the water wash was neutral to pH. It was then agitated in 1% NaOH solution for 12 hours, then washed with water till the filtrate was neutral to pH. The obtained polymer was filtered, soaked in acetone, again filtered and then dried in a vacuum oven at 100° C. for 5 days.

Example 1b: Preparation of Co-ABPBI-1

[0083] A 2300 g of PPA, 100 g of 3,4-diaminobenzoic acid and 14.1 g of 2,6-naphthalenedicarboxylic acid were added to a three-neck round flask. The temperature was raised to 170° C. and maintained for 3.5 h. The temperature was then lowered to 140° C., 13.9 g of 3,3′-diaminobenzidine was added, stirred for 0.5 h and the temperature was raised to 170° C. for 1 h. The temperature was further elevated to 200° C. and maintained for 5 h. The polymer was precipitated in water and processed as given in Example 1a in order to obtain the dried polymer.

Example 1c: Preparation of Co-ABPBI-2

[0084] The co-ABPBI-2 was prepared by adding 2300 g of PPA, 60 g of 3,4-diaminobenzoic acid and 32.8 g of isophthalic acid in a reactor. The temperature was raised to 170° C. and maintained for 3.5 h with stirring. The temperature was lowered down to 140° C., 42.3 g of 3,3′-diaminobenzidine was added and stirred for 0.5 h. The temperature was then raised to 170° C. and stirred for 1 h. The temperature was further elevated to 200° C. and the reaction mixture was stirred for 5 h. The polymer was precipitated in water, cut into pieces and processed as given in Example 1a in order to obtain the polymer.

Example 1d: Preparation of Co-ABPBI-3

[0085] The co-ABPBI-3 was prepared as given in Example-1c, except, the terephthalic acid was used in place of isophthalic acid.

Example 1e: Preparation of Co-ABPBI-4

[0086] The co-ABPBI-4 was prepared by adding 3070 g of PPA, 60 g of 3,4-diaminobenzoic acid and 8.5 g of 2,6-naphthalenedicarboxylic acid into a reactor. The temperature of the reactor was raised to 170° C. and maintained for 1.5 h. Then 26.2 g of terephthalic acid was added and stirred for 1 h. The temperature was lowered down to 140° C. and 42.3 g of 3,3′-diaminobenzidine was added and stirred for 0.5 h. The temperature was again raised to 170° C. for 1 h and then to 200° C. and maintained for 3 h while stirring. The polymer was precipitated in water, cut into pieces and processed as given in Example 1a in order to obtain the polymer in dry form.

Example 2: Preparation of Substituted Polymers

Example 2a

[0087] The tert-butyl group substituted polybenzimidazole, PBI-BuI was synthesized as given in prior art (J. Membr. Sci. 286 (2006) 161).

Example 2b

[0088] The hexafluoroisopropylidene substituted polybenzimidazole, PBI-HFA was prepared as given in the prior art. (J. Membr. Sci. 286 (2006) 161).

Example 2c

[0089] The dimethylsubstituted polybenzimidazole, DMPBI-BuI was prepared as given in the prior art (Eur. Polym. J. 45 (2009) 3363).

Example 2d

[0090] The di-tert-butylbenzyl substituted polybenzimidazole was prepared as given in the prior art (Eur. Polym. J. 45 (2009) 3363).

Example 2e

[0091] The N-sodium salt of PBI-BuI was reacted with methyl iodide to form a polyionic liquid, as given in the prior art (US-20130184412A1, Polym. Chem. 5 (2014), 4083). A 3-necked round-bottomed flask was charged with 600 ml of dry DMSO, added 20 g of PBI (PBI-I or PBI-BuI) and 2.1 molar equivalents of NaH (60% mineral oil dispersion form) and stirred under dry N.sub.2 atmosphere at ambient temperature for 24 h. The reaction mixture was then heated at 80° C. for an h. The reaction mixture was allowed to cool to ambient and 4.2 equivalent of methyl iodide was added. The reaction temperature was elevated to 80° C. and further stirred for 24 h, the temperature was lowered to ambient and then precipitated in a mixture of toluene-acetone (1:1). The obtained golden yellow precipitate was dried at 80° C. for 24 h. It was further purified by dissolving in DMSO and re-precipitation in the same non-solvent. The obtained polymer was dried at 80° C. for three days.

Example 2f

[0092] The iodide anion of polyionic liquid as synthesized in Example 2e was exchanged as given in the prior art (WO-2012035556A1, Polym. Chem. 5 (2014), 4083). A two necked flask equipped with calcium chloride guard tube was charged with 5 g of a [TMPBI-BuI][I] and 100 ml of DMF. After the complete dissolution, 2 molar equivalent of AgBF.sub.4 was added while stirring. The AgI precipitated and the anion exchanged polymer remained in the solution. The precipitated AgI was removed by centrifugation and the anion exchanged polymer ([TMPBI-BuI][BF.sub.4]) was recovered from the supernatant by solvent evaporation.

Example 3: Preparation of Dope Solution

Example 3a

[0093] A round-bottomed flask equipped with a mechanical stirrer was charged with 975 g of methanesulphonic acid, heated to 80° C., added a single polymer as prepared in Example 1a-e and stirred for 24 h to obtain a dope solution of a different polymer.

Example 3b

[0094] A round-bottomed flask equipped with a mechanical stirrer was charged with 970 g of MSA, 15 g of ABPBI, as synthesized in Example 1a and 15 g of co-ABPBI as synthesized in Example 1d and heated to 80° C. for 24 h.

Example 3c

[0095] A round-bottomed flask equipped with a mechanical stirrer was charged with 930 g of N,N-dimethyl acetamide (DMAc), 70 g of DMPBI-BuI, synthesized as given in Example 2c, heated to 80° C. for 24 h while stirring to make a dope solution.

Example 3d: Preparation of Dope Solution Using Polyetherimide

[0096] The dope solution was prepared in a round-bottomed flask by charging 292 g of N-methyl-2-pyrrolidone (NMP) and 108 g of polyetherimide (Ultem-1000 grade) and stirring using mechanical stirrer for 48 hours at ambient temperature.

Example 3e: Preparation of Dope Solution Using Polyacrlonitrile (PAN)

[0097] A round-bottomed flask was charged with 740 g of N,N-dimethylformamide (DMF), heated at 60° C., added 140 g of PAN and 40 g of citric acid (CA) and stirred for 48 h.

Example 3f: Preparation of Dope Solution Using PBI-BuI that was Synthesized as Given in Example 2a

[0098] A round-bottomed flask was charged with 770 g of N-methyl-2-pyrrolidone (NMP) and 30 g of lithium chloride (LiCl). After the dissolution of LiCl, 200 g of PBI-BuI was added. The heating at 80° C. was done for 36 hours.

Example 3g: Preparation of Dope Solution Using PBI-HFA that was Synthesized as Given in Example 2b

[0099] A round-bottomed flask was charged with 810 g of NMP and 40 g LiCl. A 150 g of PBI-HFA was added and stirred at 80° C. for 30 hours.

Example 4: Preparation of Hollow Fiber Membrane

Example 4a

[0100] The hollow fiber membranes using the dope solution as prepared in Example 3a-c were prepared by phase inversion process as known in the art [U.S. Pat. No. 6,986,844B2]. In a typical procedure, the hollow fiber membranes were prepared by a dry-jet, wet spinning process. A tube-in-orifice type spinneret was used to spin the hollow fiber membrane. The water was used as a bore fluid as well as external coagulation bath. The membranes were spun at ambient temperature.

Example 4b

[0101] The reaction mixture as prepared in Example 1a, 1b, 1c, 1d, and 1e was further diluted with methanesulphonic acid and used as a dope solution for the preparation of hollow fiber membrane by the method as given in Example 4b.

Example 5: Preparation of Dual-Layer Hollow Fiber Membrane

Example 5a

[0102] The dope solution as prepared in Example 3a-c was used for forming the outer layer of the dual-layer membrane. The solutions as prepared in Example 3d or 3e was used as an inner layer. The dual-layer hollow fiber membrane was spun with as known in the prior art [US-20110266222]. In a typical procedure, the hollow fiber membranes were prepared by a dry-jet, wet spinning process. The water was used as a bore fluid as well as external coagulation bath. The membranes were spun at ambient temperature.

Example 5b

[0103] In another dual-layer type of hollow fiber membranes, the dope solution as prepared in Example 3f and 3g was used for forming the outer layer. The solutions as prepared in Example 3d or 3e was used for forming inner layer of the dual-layer membrane. The method was the same as used in Example 5a.

Example 6: Cross-Linking of Hollow Fiber Membranes

[0104] The dried hollow fiber membrane as prepared in Example 4a, 4b, 5a or 5b were dipped in 10% (wt./wt.) 1,4-dibromobutane in acetonitrile as a solvent. The membranes were further dried at 80° C. for 24 h. The crosslinked hollow fiber membranes were coated with 1.96 wt. % of silicone rubber in petroleum ether solution.

Example 7: Preparation of Membrane Module

[0105] The hollow fiber membrane modules as prepared in Example 4a, 4b, 5a, or 5b were potted by using two-component epoxy glue.

Example 7A: Preparation of U-Shaped Membrane Module

[0106] The hollow fiber membrane modules as prepared in Example 4a, 4b, 5a, or 5b were potted by using two-component epoxy glue.

Example 8: Transport Through Hollow Fiber Membrane Modules

Example 8a: Transport Study of NaCl

[0107] The hollow fiber membrane as spun in Example 4a (using the polymer prepared as given in Example 1a, and the dope solution as prepared in Example 3a) and the module prepared as given in Example 7 was used for this study. The NaCl solution was circulated from the shell side of the membrane, while water was circulated from the bore side of the hollow fiber membrane. In different experiments, NaCl concentration was varied as 0.1 wt. %, 0.5 wt. % and 5 wt. % in water. The concentration of shell and tube side solution was continuously monitored for NaCl concentration by using online conductivity meter for 24 h. The flux of NaCl (amount transported from shell side to tube side) for 0.1, 0.5 and 5 wt. % feed concentration was found to be 1.17×10.sup.−3, 3.31×10.sup.−2 and 2.13×10.sup.−1 g m.sup.−2h.sup.−1, respectively.

Example 8b: Transport of Inorganic Acids

[0108] The hollow fiber membrane as spun in Example 4a (using the polymer prepared as given in Example 1a, and the dope solution as prepared in Example 3a) and the U-shaped module prepared as given in Example 7 was used for this study. The transport of different acids viz., HNO.sub.3, H.sub.2SO.sub.4 or H.sub.3PO.sub.4 was evaluated at different concentrations: 0.5 M, 1 M, 1.5 M and 2M. The flux of acid (amount transported from feed side to tube side) transported on the tube side is monitored by sampling and titration. The flux data is given in Table 1. (Refer table 1)

Example 8c: Transport of Organic Acids

[0109] The hollow fiber membranes as spun in Example 4b (using the polymer prepared as given in Example 1a, and the dope solution as prepared in Example 3a) and the module prepared as given in Example 7 was used. The transport of organic acids from the feed side to the tube side (strip side) of the membrane module was evaluated using acetic acid, glycolic acid, and lactic acid. The experiments were carried out as given in Example 8b. The feed concentration for individual acid was varied from 0.5 M, 1.5M and 2M and the acid transported to the tube side was evaluated by titration. The flux data is given in Table 2.

Example 8d: Transport Using HNO.SUB.3.+Fe(NO.SUB.3.).SUB.3 .Solution

[0110] The hollow fiber membranes spun as given in Example 4a (using the polymer prepared as given in Example 1a, and the dope solution as prepared in Example 3a) and the module prepared as given in Example 7 was used for this study. The concentration of HNO.sub.3 taken in the shell (feed) side was 1M, while the concentration of Fe(NO.sub.3).sub.3 was 0.25M. The flux for HNO.sub.3 was found to be 118.8 g.Math.m.sup.−2.Math.h.sup.−1 and the flux for Fe(NO.sub.3).sub.3 was found to be 1.45×10.sup.−2 g.Math.m.sup.−2.Math.h.sup.−1, offering selectivity of HNO.sub.3 over Fe(NO.sub.3).sub.3 as 8194.

Example 8e: Transport Using H.SUB.2.SO.SUB.4.+FeSO.SUB.4 .Solution

[0111] The hollow fiber membranes spun in Example 4a (using the polymer prepared as given in Example 1a, and the dope solution as prepared in Example 3a) and module prepared as given in Example 7 was used for this study. The acid concentration on the shell (feed) side was 1M, while the concentration of FeSO.sub.4 was 0.25M. The flux H.sub.2SO.sub.4 was found to be 62.9 g.Math.m.sup.−2h.sup.−1 and the flux for FeSO.sub.4 was 7.62×10.sup.−1 g.Math.m.sup.−2.Math.h.sup.−1. The selectivity of H.sub.2SO.sub.4 over FeSO.sub.4 was found to be 83.

Example 8f: Pervaporation Using Methanol-Water

[0112] The hollow fiber membranes spun in Example 4b (using the polymer prepared as given in Example 1a, and the dope solution as prepared in Example 3a) and module prepared as given in Example 7 was used for this study. The 90% aqueous methanol was circulated from the shell side. The tube side pressure was maintained at 700 mbar. The permeate flux was found to be 574 g.Math.m.sup.−2.Math.h.sup.−1 with the selectivity of water over methanol as 55.

Example 8g: Forward Osmosis Using NaCl as a Draw Solution

[0113] The hollow fiber membrane as spun in Example 4a (using the polymer prepared as given in Example 1a, and the dope solution as prepared in Example 3a) and module prepared as given in Example 7 was used for this study. A 2M aqueous NaCl solution was taken as a draw solution on the tube side, while DI water was used as feed solution on the shell side. The water flux was found to be 193.73 g.Math.m.sup.−2.Math.h.sup.−1.

Example 8h: Pervaporation Using IPA-Water

[0114] The dual-layer hollow fiber membranes spun in Example 5a (outer layer formed using dope solution given in Example 3a and an inner layer formed using dope solution given in Example 3d) were used to make the module as given in Example 7. A solution made with 75% IPA and 25% water was circulated from the shell side of the module. The tube side pressure was maintained at 700 mbar. The permeate flux was 33 g.Math.m.sup.−2.Math.h.sup.−1. The composition of the permeate was 94% water and 6% IPA.

Example 81: Forward Osmosis Study

[0115] The module was prepared as given in Example 7 using dual-layer hollow fibers prepared in Example 5a (outer layer formed using dope solution given in Example 3a, based on polymer prepared in Example 1a and inner layer formed using dope solution given in Example 3e). A 2M NaCl was used as the draw solution on the tube side and DI water was circulated on the shell side. The water flux obtained was 593 g.Math.m.sup.−2.Math.h.sup.−1 with NaCl rejection as 99.49%.

Example 8j: Transport of Acids in Dual-Layer Hollow Fiber Membrane

[0116] The hollow fiber membranes spun in Example 5a (outer layer formed using dope solution given in Example 3b based on polymer prepared in Example 1c and inner layer formed using dope solution given in Example 3d) were used to make module as given in Example 7. The flux of 0.5M HNO.sub.3 was 176 g.Math.m.sup.−2.Math.h.sup.−1; while the flux of 1M lactic acid was 68 g.Math.m.sup.−2.Math.h.sup.−1.

Example 8k: Gas Permeation Through Dual Layer Hollow Fiber Membrane Coated with Silicon Rubber

[0117] The hollow fiber membrane prepared as given in Example 5b (outer layer formed using dope solution given in Example 3f and inner layer formed using dope solution given in Example 3d) were used to prepare a module as given in Example 6 and 7. The individual gas (He, N.sub.2, CO.sub.2 or CH.sub.4) was pressurized to the shell side of the membrane at either 50, 60 or 70 psi. The permeation analysis is as given in Table 3. Refer Table 3

Advantages of the Invention

[0118] The polymeric materials with high Tg and chemical stability, like substituted PBI-BuI and PBI-HFA which offers high permeance and selectivity as a skin layer and, the core of which will be composed of commercial low-cost polymers. [0119] The advantages of using ABPBI based membrane (over conventional PBI) is their higher NH-group density (molar mass of N—H group per repeat unit of a PBI) that is anticipated to lead to high acid complexation ability. [0120] The membrane can be prepared solely with one polymer or dual-layer membranes with the inner and outer layer of adequate polymers along with ABPBI or its copolymers. [0121] The hollow fiber membranes prepared solely with ABPBI or its copolymer can be used under harsh environment. [0122] These hollow fibers can cater to the need of various separations such as chemodialysis, gas separation, pervaporation, reverse osmosis, forward osmosis, etc.