A system for generating sterile water is provided, including: a liquid holding container having thereon a container outlet; a filtration device including therein a low-pressure-differential pathogen filtration portion, wherein the filtration device has a filtration inlet and a filtration outlet; and a gas tube; wherein the container outlet is connected to the filtration inlet; wherein the filtration inlet has a gas hole with one end connected to the gas hole and the other end having a buoy; wherein the sterile water is substantially pathogen-free.

The present invention is directed to affinity chromatography devices that separate a targeted protein or antibody from an aqueous mixture containing the targeted protein or antibody. The chromatography device may contain a stacked membrane assembly or a wound membrane assembly. The membrane assemblies include at least one polymer membrane that contains therein inorganic particles. The polymer membrane and/or the inorganic particles have an affinity ligand bonded thereto. The affinity ligand may be a protein, an antibody, or a polysaccharide that reversibly binds to the targeted protein or antibody. The chromatography device may be repeatedly used and may be cleaned with a caustic solution between uses. The chromatography devices may have a dynamic binding capacity (DBC) of at least 30 mg/ml (or 0.07 micromol/ml) at 10% breakthrough at a residence time of 20 seconds or less.

The present invention is directed to affinity chromatography devices that separate a targeted protein or antibody from an aqueous mixture containing the targeted protein or antibody. The chromatography device may contain a stacked membrane assembly or a wound membrane assembly. The membrane assemblies include at least one polymer membrane that contains therein inorganic particles. The polymer membrane and/or the inorganic particles have an affinity ligand bonded thereto. The affinity ligand may be a protein, an antibody, or a polysaccharide that reversibly binds to the targeted protein or antibody. The chromatography device may be repeatedly used and may be cleaned with a caustic solution between uses. The chromatography devices may have a dynamic binding capacity (DBC) of at least 30 mg/ml (or 0.07 micromol/ml) at 10% breakthrough at a residence time of 20 seconds or less.

A selectively permeable membrane device for separating a first fluid from a second fluid in a flow can include a membrane conduit configured to receive the flow and to allow permeation of the first fluid therethrough, and configured to not allow permeation of the second fluid. The device can include a residence time enhancing structure disposed within the membrane conduit and configured to increase residence time of the flow within the membrane conduit.

The present invention is directed to affinity chromatography devices that separate a targeted protein or antibody from an aqueous mixture containing the targeted protein or antibody. The chromatography device may contain a stacked membrane assembly or a wound membrane assembly. The membrane assemblies include at least one polymer membrane that contains therein inorganic particles. The polymer membrane and/or the inorganic particles have an affinity ligand bonded thereto. The affinity ligand may be a protein, an antibody, or a polysaccharide that reversibly binds to the targeted protein or antibody. The chromatography device may be repeatedly used and may be cleaned with a caustic solution between uses. The chromatography devices may have a dynamic binding capacity (DBC) of at least 30 mg/ml (or 0.07 micromol/ml) at 10% breakthrough at a residence time of 20 seconds or less.

The present invention is directed to affinity chromatography devices that separate a targeted protein or antibody from an aqueous mixture containing the targeted protein or antibody. The chromatography device may contain a stacked membrane assembly or a wound membrane assembly. The membrane assemblies include (1) at least one polymer membrane that contains therein inorganic particles and (2) at least one impermeable layer (e.g., a thermoplastic polymer in a solid state). The polymer membrane and/or the inorganic particles have an affinity ligand bonded thereto. The affinity ligand may be a protein, an antibody, or a polysaccharide that reversibly binds to the targeted protein or antibody. The chromatography device may be repeatedly used and may be cleaned with a caustic solution between uses. The chromatography devices has a dynamic binding capacity (DBC) of at least 30 mg/ml (or 0.07 micromol/ml) at 10% breakthrough at a residence time of 20 seconds or less.

The present inventions are directed to systems and methods to increase the removal of PFAS and other recalcitrant organic compound contaminants from water, and particularly ground and drinking water, using sub-micron powdered activated carbon.

The present invention relates to a fuel cell membrane humidifier capable of improving humidification efficiency by performing two-stage humidification, and a fuel cell system comprising same. A fuel cell membrane humidifier according to an embodiment of the present invention comprises: a dry air supply means; a fuel cell membrane humidifier which performs two-stage humidification on the dry air supplied from the dry air supply means; a fuel cell stack for generating energy and humid exhaust gas by reacting the humidified air supplied from the fuel cell membrane humidifier with hydrogen; and a bypass flow path for bypassing a portion of the exhaust gas generated in the fuel cell stack. The fuel cell membrane humidifier comprises: a mid-case; a cap which is fastened with the mid-case and has a bypass inlet connected to the bypass flow path; a mixing humidifier which performs mixed humidification by mixing the dry air introduced through the cap and the exhaust gas introduced through the bypass inlet; and at least one cartridge which is disposed in the mid-case and accommodates a plurality of hollow fiber membranes that perform moisture exchange.

An air dehydration module includes polymeric fibers for separating water vapor from air, and also includes a carbon filter material, positioned at an outlet end of the module, and within the same pressure vessel which houses the fibers. The module may generate its own sweep stream, in which case a portion of its output is directed to flow through an orifice, towards the inlet end of the module. In an alternative embodiment, the sweep gas is produced by a distinct gas-separation module, which receives an input stream from the output of the dehydration module. The dehydration module produces clean and dry air which can be used as is, or as an input stream to an air separation module.

A process for removing Co.sup.2+, Pb.sup.2+, Cd.sup.2+ and Cr.sup.3+ toxins from bodily fluids is disclosed. The process involves contacting the bodily fluid with an ion exchange composition to remove the metal toxins in the bodily fluid, including blood and gastrointestinal fluid. Alternatively, blood can be contacted with a dialysis solution which is then contacted with the ion exchange composition. The ion exchange compositions are represented by the following empirical formula:
A.sub.mZr.sub.aTi.sub.bSn.sub.cM.sub.dSi.sub.xO.sub.y. A composition comprising the above ion exchange compositions in combination with bodily fluids or dialysis solution is also disclosed. The ion exchange compositions may be supported by porous networks of biocompatible polymers such as carbohydrates or proteins.