Microporous polybenzimidazole particulates

Claim 2

Microporous particles of polybenzimidazole resins selected from a group consisting of polybenzimidazoles and modified polybenzimidazoles functionalized by treatment with an organic or inorganic acid, said polybenzimidazole resin consisting essentially of reoccurring units selected from the formula: ##STR4## wherein R is a tetravalent aromatic nucleus, preferably symmetrically substituted, with the nitrogen atoms forming the benzimidazole rings being paired upon adjacent carbon atoms, i.e., ortho carbon atoms, of the aromatic nucleus, and R' is a member of the class consisting of (1) an aromatic ring, (2) an alkylene group, and (3) a heterocyclic ring from the class consisting of (a) pyridine, (b) pyrazine, (c) furan, (d) quinoline, (e) thiophene. and (f) pyran, and the formula ##STR5## wherein Z is an aromatic nucleus having the nitrogen atoms forming the benzimidazole ring paired upon adjacent carbon atom of the aromatic nucleus, said microporous particles being characterized by a reduced bulk density, a specific surface area of at least about 10 m 2 /g, a porosity of at least about 10%, and an average pore diameter of from about 50 to about 500 angstroms.

Claim 3

The microporous particles of claim 1 in the form of substantially spherical beads.

Claim 4

The microporous particles of claim 2, wherein said particles comprise polybenzimidazole.

Claim 5

The microporous particles of claim 2, wherein said particles comprise a cation exchange polybenzimidazole resin having inorganic or organic acid groups covalently bonded thereto.

Claim 6

The microporous particles of claim 4, wherein said acid groups comprise sulfonate groups.

Claim 7

The microporous particles of claim 2, wherein said particles comprise an anion exchange polybenzimidazole resin having inorganic or organic acid groups ionically bonded thereto.

Claim 8

The microporous particles of claim 3, 4, 5 or 6, wherein said polybenzimidazole comprises poly-2,2'-(m-phenylene)-5,5'-bibenzimidazole.

Claim 9

The microporous particles of claim 7, wherein said particles have a porosity of at least about 20%; a specific surface area of at least about 25 m 2 /g; an average pore diameter of from about 75 to about 250 Angstroms; and an average particle size of from about 10 to about 1000 microns.

Claim 10

Microporous particles of polybenzimidazole resin selected from the group consisting of poly-2,2'-(m-phenylene)-5,5'-bibenzimidazole and sulfonated poly-2,2'-(m-phenylene)-5,5'-bibenzimidazole having an average particle size of from about 10 to about 1000 microns, a reduced bulk density, a surface area of at least 10 m 2 /g. a porosity of at least about 10%, and an average pore diameter of from about 50 to about 500 Angstroms.

Claim 11

Microporous particles of polybenzimidazole resin selected from the group consisting of poly-2,2'-(m-phenylene)-5,5'-bibenzimidazole and sulfonated poly-2,2'-(m-phenylene)-5,5'-bibenzimidazole having an average particle size of from about 10 to about 1000 microns, a reduced bulk density, a surface area of at least 10 m 2 /g. a porosity of at least about 10%, and an average pore diameter of from about 50 to about 500 Angstroms.

Claim 12

The microporous particles of claim 9, wherein said polybenzimidazole resin comprises sulfonated poly-2,2'-(m-phenylene)-5,5'-bibenzimidazole having covalently bonded sulfonate groups and a degree of sulfonation corresponding to a sulfur content of from about 1 to about 10% by weight.

Claim 13

A process for the preparation of microporous particles of polybenzimidazole resin suitable for use as the stationary phase in chromatographic processes or supported chemical reactions, comprising the steps of: (a) forming in a suitable solvent a 2 to about 10% solution of a polybenzimidazole resin consisting essentially of reoccurring units selected from the formula: ##STR6## wherein R is a tetravalent aromatic nucleus, preferably symmetrically substituted, with the nitrogen atoms forming the benzimidazole rings being paired upon adjacent carbon atoms, i.e., ortho carbon atoms, of the aromatic nucleus, and R' is a member of the class consisting of (1) an aromatic ring, (2) an alkylene group, and (3) a heterocyclic ring from the class consisting of (a) pyridine, (b) pyrazine, (c) furan, (d) quinoline, (e) thiophene, and (f) pyran, and the formula: ##STR7## wherein Z is an aromatic nucleus having the nitrogen atoms forming the benzimidazole ring paired upon adjacent carbon atoms of the aromatic nucleus; (b) emulsifying said polybenzimidazole solution with a non-polar organic solvent in a volume ratio of polybenzimidazole solution to non-polar organic solvent of from about 1:2 to about 1:4 under conditions of shear sufficient to produce substantially spherical droplets of polybenzimidazole resin; (c) precipitating said spherical droplets of polybenzimidazole resin from said emulsion in the form of substantially spherical microporous beads by contacting said emulsion with a non-solvent for said polybenzimidazole resin; and (d) recovering the resulting microporous particles of polybenzimidazole resin.

Claim 14

A process for the preparation of microporous particles of polybenzimidazole resin suitable for use as the stationary phase in chromatographic processes or supported chemical reactions, comprising the steps of: (a) forming in a suitable solvent a 2 to about 10% solution of a polybenzimidazole resin consisting essentially of reoccurring units selected from the formula: ##STR6## wherein R is a tetravalent aromatic nucleus, preferably symmetrically substituted, with the nitrogen atoms forming the benzimidazole rings being paired upon adjacent carbon atoms, i.e., ortho carbon atoms, of the aromatic nucleus, and R' is a member of the class consisting of (1) an aromatic ring, (2) an alkylene group, and (3) a heterocyclic ring from the class consisting of (a) pyridine, (b) pyrazine, (c) furan, (d) quinoline, (e) thiophene, and (f) pyran, and the formula: ##STR7## wherein Z is an aromatic nucleus having the nitrogen atoms forming the benzimidazole ring paired upon adjacent carbon atoms of the aromatic nucleus; (b) emulsifying said polybenzimidazole solution with a non-polar organic solvent in a volume ratio of polybenzimidazole solution to non-polar organic solvent of from about 1:2 to about 1:4 under conditions of shear sufficient to produce substantially spherical droplets of polybenzimidazole resin; (c) precipitating said spherical droplets of polybenzimidazole resin from said emulsion in the form of substantially spherical microporous beads by contacting said emulsion with a non-solvent for said polybenzimidazole resin; and (d) recovering the resulting microporous particles of polybenzimidazole resin.

Claim 15

A process for the preparation of microporous particles of polybenzimidazole resin suitable for use as the stationary phase in a chromatographic process or supported chemical reactions, comprising the steps of: (a) forming in a suitable solvent a 2 to 20% by weight solution of a polybenzimidazole resin consisting essentially of reoccurring units selected from the formula: ##STR8## wherein R is a tetravalent aromatic nucleus, preferably symmetrically substituted, with the nitgrogen atoms forming the benzimidazole rings being paired upon adjacent carbon atoms i.e., ortho carbon atoms, of the aromatic nucleus, and R' is a member of the class consisting of (1) an aromatic ring, (2) an alkylene group, and (3) a heterocyclic ring from the class consisting of (a) pyridine, (b) pyrazine, (c) furan, (d) quinoline, (e) thiophene, and (f) pyran, and the formula: ##STR9## wherein Z is an aromatic nucleus having the nitrogen atoms forming the benzimidazole ring paired upon adjacent carbon atoms of the aromatic nucleus; (b) converting the solution of step (a) into a stream of finely divided liquid droplets; (c) quenching said stream of liquid droplets with a non-solvent for the polybenzimidazole resin to produce solidified microporous particles of polybenzimidazole resin; and (d) recovering the resulting microporous particles of polybenzimidazole resin.

Claim 16

A process for the preparation of microporous particles of polybenzimidazole resin suitable for use as the stationary phase in a chromatographic process or supported chemical reactions, comprising the steps of: (a) forming in a suitable solvent a 2 to 20% by weight solution of a polybenzimidazole resin consisting essentially of reoccurring units selected from the formula: ##STR8## wherein R is a tetravalent aromatic nucleus, preferably symmetrically substituted, with the nitgrogen atoms forming the benzimidazole rings being paired upon adjacent carbon atoms i.e., ortho carbon atoms, of the aromatic nucleus, and R' is a member of the class consisting of (1) an aromatic ring, (2) an alkylene group, and (3) a heterocyclic ring from the class consisting of (a) pyridine, (b) pyrazine, (c) furan, (d) quinoline, (e) thiophene, and (f) pyran, and the formula: ##STR9## wherein Z is an aromatic nucleus having the nitrogen atoms forming the benzimidazole ring paired upon adjacent carbon atoms of the aromatic nucleus; (b) converting the solution of step (a) into a stream of finely divided liquid droplets; (c) quenching said stream of liquid droplets with a non-solvent for the polybenzimidazole resin to produce solidified microporous particles of polybenzimidazole resin; and (d) recovering the resulting microporous particles of polybenzimidazole resin.

Claim 17

The process of claim 11, wherein said solvent of step (a) is N,N-dimethylacetamide or concentrated sulfuric acid; said non-polar organic solvent of step (b) is a halogenated solvent or an aliphatic petroleum solvent; and said non-solvent of step (c) comprises an aliphatic alcohol of from about one to four carbon atoms.

Claim 18

The process of claim 11, wherein said non-solvent of step (c) comprises methanol.

Claim 19

The process of claim 11, wherein the emulsion of step (b) further comprises up to about 2% by weight of a surfactant to stabilize said emulsion, and up to about 5% by weight of a pore forming additive.

Claim 20

The process of claim 11, further comprising the step of treating the recovered particles of polybenzimidazole resin with a solution of an organic or inorganic acid having an acid concentration of from about 1 to about 10 percent by weight in order to modify the functional properties of the resin.

Claim 21

The process of claim 11, wherein up to about 15% by weight of an organic or inorganic acid is included in said polybenzimidazole solution of step (a) in order to modify the functional properties of the resin.

Claim 22

The process of claim 13, wherein the solvent of step (a) is concentrated sulfuric acid, and said process further comprises the step of heat setting the recovered microporous polybenzimidazole particles at a temperature of greater than 180° C. for at least about 30 minutes in order to covalently sulfonate the polybenzimidazole resin.

Claim 23

The process of claims 16 or 17, wherein said acid is selected from the group consisting of sulfuric acid, organic sulfonic acids and mixtures thereof, and said process further comprises heat setting the acid treated microporous resin particles at a temperature of greater than 180° C. for at least about 30 minutes in order to covalently sulfonate the polybenzimidazole resin.

Claim 24

The process of claim 12, wherein the solution of step (a) is convered into a stream of liquid droplets by spraying techniques.

Claim 25

The process of claim 20, wherein said solvent of step (a) is N,N'-dimethylacetamide or concentrated sulfuric acid; and said non-solvent of step (c) comprises an aliphatic alcohol of from about one to four carbon atoms.

Claim 26

The process of claim 21, wherein said non-solvent of step (c) comprises methanol.

Claim 27

The process of claim 12, wherein the solution of step (a) further comprises up to about 5% by weight of a pore forming additive.

Claim 28

The process of claim 12, further comprising the step of treating the recovered particles of polybenzimidazole resin with a solution of an organic or inorganic acid having an acid concentration of from about 1 to about 10 percent by weight in order to modify the functional properties of the resin.

Claim 29

The process of claim 12, wherein up to about 15% by weight of an organic or inorganic acid is included in said polybenzimidazole solution of step (a) in order to modify the functional properties of the resin.

Claim 30

The process of claim 12, wherein the solvent of step (a) is concentrated sulfuric acid, and said process further comprises the step of heat setting the recovered microporous polybenzimidazole particles at a temperature of greater than 180° C. for at least about 30 minutes in order to covalently sulfonate the polybenzimidazole resin.

Claim 31

The process of claim 24 or 25, wherein said acid is selected from the group consisting of sulfuric acid, organic sulfonic acids and mixtures thereof, and said process further comprises heat setting the acid treated microporous resin particles at a temperature of greater than 180° C. for at least about 30 minutes in order to covalently sulfonate the polybenzimidazole resin.