Disclosed are copolymers which are useful in hydrophilically modifying porous fluoropolymer supports. An example of the copolymers is: ##STR00001##
Also disclosed are a method of preparing such copolymers, a method of modifying porous fluoropolymer surfaces, and hydrophilic fluoropolymer porous membranes prepared therefrom. Also disclosed is a method of filtering fluids by the use of the hydrophilic fluoropolymer porous membranes.

Disclosed are copolymers which are useful in hydrophilically modifying porous fluoropolymer supports. An example of the copolymers is: ##STR00001##
Also disclosed are a method of preparing such copolymers, a method of modifying porous fluoropolymer surfaces, and hydrophilic fluoropolymer porous membranes prepared therefrom. Also disclosed is a method of filtering fluids by the use of the hydrophilic fluoropolymer porous membranes.

Described herein are passive samplers, making of such samplers, and methods of use. In an example embodiment, a passive sampling membrane comprises, for example, a continuous mesoporous sequestration media having a sequestration phase and a support membrane configured to support the sequestration phase. The sequestration phase may include a hydrophobic region and a hydrophilic region. The continuous mesoporous sequestration media may be configured to simultaneously sequester polar and non-polar organic substances.

Described herein are passive samplers, making of such samplers, and methods of use. In an example embodiment, a passive sampling membrane comprises, for example, a continuous mesoporous sequestration media having a sequestration phase and a support membrane configured to support the sequestration phase. The sequestration phase may include a hydrophobic region and a hydrophilic region. The continuous mesoporous sequestration media may be configured to simultaneously sequester polar and non-polar organic substances.

The present invention relates to novel co-polymers and their use in the manufacture of porous membranes for haemodialysis application. In particular, such a co-polymer comprises a first segment comprising recurring units poly(aryl ether sulfone) [PAES recurring units], and a second segment comprising-recurring units poly(vinyl pyrrolidone) [PVP recurring units], wherein said first segment and said second segment are linked together via a group of formula —O-Ph-NH—C(═O)—C(CH.sub.3).sub.2—CH.sub.2—.

The present invention relates to novel co-polymers and their use in the manufacture of porous membranes for haemodialysis application. In particular, such a co-polymer comprises a first segment comprising recurring units poly(aryl ether sulfone) [PAES recurring units], and a second segment comprising-recurring units poly(vinyl pyrrolidone) [PVP recurring units], wherein said first segment and said second segment are linked together via a group of formula —O-Ph-NH—C(═O)—C(CH.sub.3).sub.2—CH.sub.2—.

The present invention relates to a gas separation membrane for separating a target gas species from a mixture of gas species, the membrane comprising: (i) a porous substrate having a first and second surface region between which the mixture of gas species will flow; (ii) a sealing polymer layer of different composition to the porous substrate that (a) forms a continuous coating across the second surface region of the substrate, and (b) is permeable to the mixture of gas species; and (iii) a selective polymer layer in the form of a cross linked macromolecular film that (a) is located on and covalently coupled to the sealing polymer layer, and (b) has a higher permeability to the target gas species relative to other gas species present in the mixture of gas species that is to be subjected to separation.

An article that can be used for biomaterial capture comprises (a) a porous substrate; and (b) borne on the porous substrate, a polymer comprising interpolymerized units of at least one monomer consisting of (1) at least one monovalent ethylenically unsaturated group, (2) at least one monovalent ligand functional group selected from acidic groups, basic groups other than guanidino, and salts thereof, and (3) a multivalent spacer group that is directly bonded to the monovalent groups so as to link at least one ethylenically unsaturated group and at least one ligand functional group by a chain of at least six catenated atoms.

An article that can be used for biomaterial capture comprises (a) a porous substrate; and (b) borne on the porous substrate, a polymer comprising interpolymerized units of at least one monomer consisting of (1) at least one monovalent ethylenically unsaturated group, (2) at least one monovalent ligand functional group selected from acidic groups, basic groups other than guanidino, and salts thereof, and (3) a multivalent spacer group that is directly bonded to the monovalent groups so as to link at least one ethylenically unsaturated group and at least one ligand functional group by a chain of at least six catenated atoms.

The present invention includes a treatment system and methods for removing waste or other agents from a fluid stream, the system comprising: an inlet flow path for receiving a fluid stream from a source outside the treatment system; a vessel for containing the fluid stream, the vessel comprising a permeable filter configured for biological and physical treatment of the fluid stream, the filter comprising one or more nano-thin film or polymer composite layers of carbon materials assembled in sp2 hybridized structures comprising carbon-carbon bonds, wherein the waste or agent is removed as it flows through pores in the film composite; and a drain fluidly connected to the vessel for discharging treated fluid stream from the vessel from which the waste or agents have been removed.