Abstract: A rotary filtration device having at least two members, one at least partially within the other to define a fluid gap therebetween, is disclosed. One or more filters are located on one or more of the members facing the fluid gap. Sufficient uncharged hydrophilic polar groups, preferably uncharged substituted amide groups, are located on the surface of the filter to render the surface hydrophilic.

Abstract: This invention provides a matrix comprising molecules of a suitable polymer which provides solely on the surface of the matrix sufficient uncharged substituted amide groups to render the surface hydrophilic. The invention also provides an article of manufacture comprising the matrix.Another aspect of the invention provides a method of producing a matrix having a hydrophilic surface which comprises treating molecules of a suitable polymer so as to provide solely on the surface of the matrix sufficient uncharged, hydrophilic substituted amide groups to render the surface hydrophilic.Another embodiment of the invention concerns improved methods of filtration, ultrafiltration, microfiltration, reverse osmosis, dialysis, prevaporation, sieving, affinity chromatography, affinity purification, affinity separation, or affinity adsorption which comprises using the article of manufacture.

Abstract: A membrane is produced by dissolving, in a water-miscible solvent, a water insoluble copolymer of acrylontrile with at least one monomer selected from the group consisting of an aminostyrene, a vinyl pyridine and an N-hydroxy-containing-substituent-acrylamide, casting said solution to form a thin layer of solution, contacting said solution with water thereby to coagulate the copolymer into a film, and washing away from the copolymer film the solution of solvent and water. The amine or hydroxy group of the copolymer is then activated and coupled with a ligand such as glucose isomerase, chymotrypsin or Protein A. The coupled membranes can then be used for biological separations and reactions.

Abstract: Proteins and non-protein affinity ligands are covalently bonded to trichloro-s-triazine activated supports. The activated support is prepared by reacting a water-free insoluble solid support with trichloro-s-triazine in a non-aqueous medium and neutralizing HCl generated during the reaction with a tertiary amine which does not form an insoluble complex with the trichloro-s-triazine.