Strongly acidic microporous membranes for cation exchange

Claim 2

A copolymer solute in a solution for post-treatment of the internal pores of a microporous base membrane comprising a crosslinkable acid copolymer of a strong acid monomer which is an acrylamide alkane sulfonic acid monomer having the formula: CH.sub.2 ═C(R)--CO--NH--R'SO.sub.3 --X where R is hydrogen or a lower alkyl or phenyl group; R' is a methylene group or a lower alkyl, lower cycloalkyl, aromatic, or bivalent hydrocarbon group or other bridging group having its valence bonds on different carbon atoms; and X is hydrogen or sodium, ammonium, organic amine or other salt forming atom or compound, and a crosslinkable monomer having hydroxyl crosslinking functionality selected from (1) N-methylolacrylamide alkoxyether compounds and (2) N-methylolacrylamide, hydroxyalkyl acrylates, and hydroxyalkyl methacrylates that are crosslinkable by reaction with aminoplast resins.

Claim 3

An acid copolymer according to claim where the acid monomer is selected from 2-acrylamido-2-methyl-1-propanesulfonic acid, 2-acrylamido-1-propanesulfonic acid, 3-acrylamido-3-butanesulfonic acid, 2-acrylamido-1-ethanesulfonic acid, 3-acrylamido-1-pentanesulfonic acid, and the like.

Claim 4

An acid copolymer according to claim 1 where the acid monomer is 2-acrylamido-2-methyl-1-propanesulfonic acid.

Claim 5

An acid copolymer according to claim 1 where the crosslinkable monomer is selected from N-(isobutoxymethyl)acrylamide, 2-hydroxyethyl methacrylate, 2-hydroxyethyl acrylate, 2-hydroxypropyl methacrylate, 2-hydroxypropyl acrylate, 3-hydroxypropyl methacrylate, and 3-hydroxypropyl acrylate.

Claim 6

An acid polymer according to claim 1 where the crosslinkable monomer comprises N-(isobutoxymethyl)acrylamide.

Claim 7

A process of preparing a crosslinkable acid copolymer for post-treatment of the internal pores of a porous membrane, which comprises reacting an acrylamide alkane sulfonic acid monomer having the formula: CH.sub.2 ═C(R)--CO--NH--R'--SO.sub.3 --X where R is hydrogen or a lower alkyl or phenyl group; R' is a methylene group or a lower alkyl, lower cycloalkyl, aromatic, or bivalent hydrocarbon group or other bridging group having its valence bonds on different carbon atoms; and X is hydrogen or sodium, ammonium, organic amine or other salt forming atom or compound, with a crosslinkable monomer having hydroxyl crosslinking functionality selected from (1) N-methylolacrylamide alkoxyether compounds and (2) N-methylolacrylamide, hydroxyalkyl acrylates, and hydroxyalkyl methacrylates that are crosslinkable by reaction with aminoplast resins and curing and drying the resulting copolymer; and diluting the copolymer with a solvent.

Claim 8

A process of preparing a crosslinkable acid copolymer for post-treatment of the internal pores of a porous membrane, which comprises reacting an acrylamide alkane sulfonic acid monomer having the formula: CH.sub.2 ═C(R)--CO--NH--R'--SO.sub.3 --X where R is hydrogen or a lower alkyl or phenyl group; R' is a methylene group or a lower alkyl, lower cycloalkyl, aromatic, or bivalent hydrocarbon group or other bridging group having its valence bonds on different carbon atoms; and X is hydrogen or sodium, ammonium, organic amine or other salt forming atom or compound, with a crosslinkable monomer having hydroxyl crosslinking functionality selected from (1) N-methylolacrylamide alkoxyether compounds and (2) N-methylolacrylamide, hydroxyalkyl acrylates, and hydroxyalkyl methacrylates that are crosslinkable by reaction with aminoplast resins and curing and drying the resulting copolymer; and diluting the copolymer with a solvent.

Claim 9

A process according to claim 6 where the amount of crosslinkable monomer in the copolymer is such that the crosslinked network in the resulting copolymer is strong and water resistant after drying without becoming brittle.

Claim 10

A process according to claim 6 where an aminoplast resin external crosslinking agent is used in the reaction.

Claim 11

A process according to claim 8 where the external crosslinking agent comprises a melamine-formaldehyde resin.

Claim 12

A strongly acidic charge modified microporous filter membrane comprising a base membrane having an internal microstructure throughout said base membrane comprising by post-treatment a charge modifying amount of a charge modifying agent bonded by drying and curing from a solvent to substantially all of said base membrane internal microstructure without substantial pore size reduction or pore blockage wherein the charge modifying agent is a crosslinked acid copolymer of a strong acid monomer which is an acrylamide alkane sulfonic acid monomer having the formula: CH.sub.2 ═C(R)--CO--NH--R'--SO.sub.3 --X where R is hydrogen or a lower alkyl or phenyl group; R' is a methylene group or a lower alkyl, lower cycloalkyl, aromatic, or bivalent hydrocarbon group or other bridging group having its valence bonds on different carbon atoms; and X is hydrogen or sodium, ammonium, organic amine or other salt forming atom or compound, with a crosslinkable monomer having hydroxyl crosslinking functionality selected from (1) N-methylolacrylamide alkoxyether compounds and (2) N-methylolacrylamide, hydroxyalkyl acrylates, and hydroxyalkyl methacrylates that are crosslinkable by reaction with aminoplast resins.

Claim 13

A strongly acidic charge modified microporous filter membrane comprising a base membrane having an internal microstructure throughout said base membrane comprising by post-treatment a charge modifying amount of a charge modifying agent bonded by drying and curing from a solvent to substantially all of said base membrane internal microstructure without substantial pore size reduction or pore blockage wherein the charge modifying agent is a crosslinked acid copolymer of a strong acid monomer which is an acrylamide alkane sulfonic acid monomer having the formula: CH.sub.2 ═C(R)--CO--NH--R'--SO.sub.3 --X where R is hydrogen or a lower alkyl or phenyl group; R' is a methylene group or a lower alkyl, lower cycloalkyl, aromatic, or bivalent hydrocarbon group or other bridging group having its valence bonds on different carbon atoms; and X is hydrogen or sodium, ammonium, organic amine or other salt forming atom or compound, with a crosslinkable monomer having hydroxyl crosslinking functionality selected from (1) N-methylolacrylamide alkoxyether compounds and (2) N-methylolacrylamide, hydroxyalkyl acrylates, and hydroxyalkyl methacrylates that are crosslinkable by reaction with aminoplast resins.

Claim 14

A charge modified microporous filter membrane according to claim 10 where the crosslinked copolymer comprises a monomer selected from 2-acrylamido-2-methyl-1-propanesulfonic acid, 2-acrylamido-1-propanesulfonic acid, 3-acrylamido-3-butanesulfonic acid, 2-acrylamido-1-ethanesulfonic acid, 3-acrylamido-1-pentanesulfonic acid, and the like.

Claim 15

A charge modified microporous filter membrane according to claim 10 where the acid monomer comprises 2-acrylamido-2-methyl-1-propanesulfonic acid.

Claim 16

A charge modified microporous filter membrane according to claim 10 where the crosslinked copolymer comprises a monomer selected from N-(isobutoxymethyl)acrylamide, 2-hydroxyethyl methacrylate, 2-hydroxyethyl acrylate, 2-hydroxypropyl methacrylate, 2-hydroxypropyl acrylate, 3-hydroxypropyl methacrylate, 3-hydroxypropyl acrylate, and the like.

Claim 17

A charge modified microporous filter membrane according to claim 10 where the crosslinked copolymer comprises N-(isobutoxymethyl)acrylamide.

Claim 18

A charge modified microporous filter membrane according to claim 10 where the base membrane comprises a polyethersulfone membrane.

Claim 19

A charge modified microporous filter membrane according to claim 10 where the base membrane comprises a polysulfone membrane.

Claim 20

A process for preparing a charge modified microporous filter membrane, comprising: post-treating a microporous base membrane with a dilute solution of an acid charge modifying copolymer according to claim 1 in a solvent medium that is compatible with the base membrane so that the solution contacts the base membrane and fills the internal pores thereof, the copolymer concentration being such as not to block said pores upon drying and curing; removing the solvent from the thus treated membrane; and curing the solvent-free membrane at elevated temperature sufficient to achieve bonding of the charge modifying copolymer to the base membrane.

Claim 21

A process according to claim 17 where the solution comprises a copolymer of 2-acrylamido-2-methyl-1-propanesulfonic acid.

Claim 22

A process according to claim 17 where the solution comprises a copolymer of N-(isobutoxymethyl) acrylamide.

Claim 23

A process according to claim 17 where the solution comprises a copolymer of 2-hydroxyethyl methacrylate and a separate crosslinking agent capable of reacting with hydroxyls.

Claim 24

A process according to claim 20 where the crosslinking agent is an aminoplast resin.

Claim 25

A process according to claim 17 where the base membrane comprises a polyethersulfone polymer.

Claim 26

A process according to claim 17 where the base membrane comprises a polysulfone polymer.

Claim 27

A membrane post-treatment solution of a crosslinkable acid copolymer prepared in a reaction according to claim 6 in a solvent for said monomer, copolymer and aminoplast resins.

Claim 28

A copolymer solution according to claim 24 comprising a solvent selected from water, dimethylformamide, and lower alcohols.

Claim 29

A copolymer solution according to claim 24 where the concentration of monomers of said copolymer in the total reaction solution is between about 4 and 17% by weight.