Disclosed herein are nanoporous membranes for separating a target substance from a non-target substance in a fluid medium and methods of making and use thereof. The nanoporous membranes comprise a 2D material permeated by a first and second population of pores; wherein the average pore diameter of the first population of pores is greater than or equal to the van der Waals diameter of water and less than the average size of the non-target substance in the fluid medium; wherein the average pore diameter of the second population of pores is greater than or equal to the average size of the non-target substance in the fluid medium; and wherein substantially all of the second population of pores are substantially blocked by a polymer via size-selective interfacial polymerization; such that the nanoporous membrane allows for transport of the target substance through the nanoporous membrane via the first population of pores.

Methods and systems are described herein for manufacturing oligosaccharides, including maltosyl-isomaltooligosaccharides. The methods involve removing undesired components from fermentation fluids that contain maltosyl-isomaltooligosaccharides.

Organic solvent nanofiltration membranes that include at least one polymer coated expanded polyparaxylylene (eP-PX) membrane are provided. A substrate/support layer may be positioned on one side of the ePPX membrane. In some embodiments, the substrate/support layer is sandwiched between ePPX membranes. Processes for manufacturing and using such organic solvent nanofiltration membranes are also provided. The organic solvent nanofiltration membranes are capable of separating and/or concentrating solutes from a solution comprising a lower molecular weight organic solvent with high permeability. The polymer coated ePPX membranes may also be resistant to chemical attack, resistant to gamma radiation, thermally stable, biocompatible, and strong.

The invention relates to the use of an uncoated cross-linked non-pyrolysed selective vinyl based halopolymer-membrane with a mwco of between 100 and 1000 Da, in the filtration of compounds from liquids comprising organic solvents and/or from liquids with a pH below 2 or above 12.

The disclosure relates to a method for separation and purification of N-acetyl-glucosamine, and belongs to the technical field of biological engineering. In the disclosure, a raw material solution containing N-acetyl-glucosamine is obtained by microbial fermentation or by hydrolyzing the chitin. The raw material solution is subjected to flocculation pretreatment, and continuous centrifugation or pressure filtration is performed to remove suspended solids such as microorganisms, proteins and polysaccharides to obtain clear liquid. Double-stage ion exchange chromatography is performed to remove impurities such as charged organic molecules and inorganic salts. Membrane concentration is performed to efficiently remove water to improve the concentration of the target product. Spray drying or further evaporation concentration and crystallization are performed. Finally drying is performed to obtain an N-acetyl-glucosamine crystal of which the purity is more than 99%.

The present invention relates to the isolation and purification of sialylated oligosaccharides from an aqueous medium in which they are produced.

A liquid purification system includes a system raw liquid feed unit and a filtration unit, which includes a liquid concentration device having an internal partition dividing a variable volume collection cavity for raw liquid coming from an initial stage of liquid filtration and for mixing therein concentrate and a raw liquid displacement cavity. The cavity is connected to a secondary line that supplies raw liquid to the cavity to displace concentrate from the collection cavity and to recycle raw liquid from the displacement cavity through the secondary line under pressure exerted by concentrate and raw liquid in the collection cavity. A filtration unit provides long-term contact between raw liquid and concentrate in the variable-volume collection cavity to provide smooth increase in the concentration of liquid supplied to a liquid purification device.

Provided is a high permeance nanofiltration membrane with nanoring-like structure and preparation method thereof. The membrane includes a base film and a polyamide layer having nanoring-like structure morphology on its surface. The method includes: (1) formulating a piperazine nanoemulsion containing a surfactant, vegetable oil, piperazine and water; and (2) infiltrating a base film with the piperazine nanoemulsion, and removing excess droplets from the surface of the base film to obtain a treated base film; covering the surface of the treated base film with a solution of trimesoyl chloride in n-hexane to perform interfacial polymerization; and drying the resulting membrane. Introduction of nano-oil droplets into aqueous phase as templates to construct nanoring-like structure morphology on the surface of the polyamide layer significantly increases the specific surface area and free volume of the polyamide layer without losing the salt rejection rate of the membrane, thereby greatly improving its water permeance.

The present invention relates to modification to permeate channels and permeate materials in a cross-flow filtration system to improve performance in counter current filtration having both retentate channels and permeate channels wherein a solution is pumped through one of the channels and drawn through a membrane to one of the other channels to assist in positive pressure driven filtration by using the osmotic pressure, concentration, or preferential solubility difference between the retentate and permeate flow streams thereby increasing or altering the flux through the membrane separating the flow streams.

A process and an apparatus for purifying a phosphate containing acidic solution (P1) containing impurities through a nanofiltration station (2) includes a number of nanofiltration membrane units arranged in series. At least one permeate recirculation loop, branching off the retentate side of the first membrane unit (M1) and closing the loop at the entry line (1e) to combine at least one of three permeates with the phosphate containing acidic solution (P1), the three permeate recirculation loops include: a first recovery recirculation loop, a first exit recirculation loop, and a second recovery recirculation loop.