An inline filter housing with a biodegradable, hydrophilic material that operates in conjunction with a field sampling apparatus to both concentrate field sampled environmental DNA particles from water samples and to automatically preserve the captured DNA via desiccation, thus avoiding filter membrane transfer steps, chemicals or cold storage preservation requirements. The hydrophilic filter housing is capable of rapidly preserving the field sampled environmental DNA captured on the filter membrane at ambient field temperatures.

A membrane module includes a housing. The housing includes a housing, comprising: a first plurality of porous hollow fiber membranes, and a second plurality of porous hollow fiber membranes different from the first plurality of porous hollow fiber membranes. The first plurality of porous hollow fiber membranes has a first length, and the second plurality of porous hollow fiber membranes has a second length that is at least 1.1 times greater than the first length. The membrane module can be used in separation methods, such as membrane distillation methods.

A filtration module for filtering a process medium in a bioprocess including a process flow path for a process medium, a filter membrane coupled to the process flow path, and a sampling membrane coupled both to the process flow path and to a sampling flow path for extracting a sample from the process medium. The sampling flow path guides the extracted sample to a sampling outlet of the filtration module or to an analyzer integrated into the filtration module. A filtration assembly including the filtration module and an analyzer coupled to the sampling outlet of the filtration module. A method of sampling during a bioprocess including providing such a filtration module, urging a process medium through the process flow path, filtering the process medium by using the filter membrane, extracting a sample from the process medium by using the sampling membrane, and guiding the extracted sample to a sampling outlet.

A process for the efficient transfer of molecules between phases employing mesoporous poly (aryl ether ketone) hollow fiber membranes is provided. The method addresses the controlled transfer of reactants into and removal of reaction products from a reaction media and the removal and separation of target molecules from process streams by membrane-assisted liquid-liquid extraction. A number of possible modes of liquid-liquid extraction are possible according to the invention by utilizing porous poly (aryl ether ketone) hollow fiber membranes of Janus-like structure that exhibit a combination of hydrophilic and hydrophobic surface characteristics. The method of the present invention can address the continuous manufacture of chemicals in membrane reactors and is useful for a broad range of separation applications, including separation and recovery of active pharmaceutical ingredients.

Methods and systems for the extraction of metals from an aqueous feed solution containing the metal ions. The aqueous feed solution is contacted with one side of a hydrophilic membrane support while an organic liquid is contacted with an opposite side of the hydrophilic membrane support. Metal ions migrate from the aqueous feed solution through the membrane support and into the organic liquid. The metal ions may be re-extracted from the organic liquid using a strip solution. The steps of extraction and reextraction may be carried out in a system including two hollow fiber membrane modules that each include a plurality of hydrophilic polymer hollow fibers.

A nanofiltration membrane with a high flux for selectively removing hydrophobic endocrine disrupting chemicals and a preparation method thereof are provided. The method includes the following steps: immersing a porous support layer into a first solution, removing excess droplets from a surface of the support layer after taking the support layer out of the first solution, and then immersing the support layer attached with the first solution into a second solution for an interfacial polymerization reaction, followed by washing after completion of the reaction to obtain the subject nanofiltration membrane. The first solution is an aqueous solution containing a polyamine monomer and an acid binding agent, and the second solution is an organic solution containing an acid chloride monomer and a metal-organic framework.

The present disclosure provides the synthesis of an imidazolium-based functional ionic liquid copolymer (PMMA-b-PIL-R*) and a preparation method of an alloy ultra-filtration membrane. Firstly, PMMA-b-PIL-R* is prepared from methyl methacrylate (MMA) and polymerizable imidazolium-based functional ionic liquid (IL-R*) containing double bonding as the reactive monomers through sequential radical polymerization. With the use of a non-solvent induced phase separation method, PMMA-b-PIL-R* is introduced into the body of a polymeric membrane material, so as to prepare an alloy ultra-filtration membrane. A hydrogen-bond interaction is generated between the carbonyl in the molecular chain of PMMA-b-PIL-R* and the H . . . C—Cl structure in the molecular chain of the polymeric membrane material, which enhances the compatibility between the molecular chains of PMMA-b-PIL-R* and the polymeric membrane material, so that it can be stable in the ultra-filtration membrane; the imidazole groups and functional groups in the molecular chain of PMMA-b-PIL-R* can provide a good hydrophilicity.

The present invention relates to a separation membrane including an organic polymer resin, in which a volume V1 of fine pores having a pore diameter of 100 nm or more is 0.3 cm.sup.3/g or more and 0.5 cm.sup.3/g or less, a volume V2 of fine pores having a pore diameter of less than 100 nm is 0.02 cm.sup.3/g or more and less than 0.1 cm.sup.3/g, and a ratio V1/V2 of the fine pore volume V1 to the fine pore volume V2 is 3 or more and 60 or less.

Disclosed are compositions that may be useful for forming synthetic membranes, methods of forming membranes therefrom, and membranes. In an embodiment, a membrane comprises a free hydrophilic polymer comprising a polyoxazoline, and a polyurethane, the polyurethane comprising a backbone comprising the reaction product of a diisocyanate, a polymeric aliphatic 5 diol, and optionally a chain extender.

An acidic gas separation membrane sheet causes an acidic gas to selectively permeate therethrough. The acidic gas separation membrane sheet includes a first porous layer, a hydrophilic resin composition layer, and a second porous layer in this order. A second peel strength between the second porous layer and the hydrophilic resin composition layer is less than a first peel strength between the first porous layer and the hydrophilic resin composition layer. An average value of the second peel strength is within a range of greater than or equal to 5 N/m and less than or equal to 500 N/m.