A filtration membrane including a first layer having a triamine-functionalized polysilicate mesoporous material, a second layer including a polysulfone; and a third layer including a polyester terephthalate is described. An orthosilicate group of the triamine-functionalized polysilicate mesoporous material is bonded to a silicon atom of a silicon-containing triamine to form a triamine-functionalized polysilicate backbone, wherein the silicon-containing triamine and one or more tetramines are covalently crosslinked with terephthaloyl chloride to form a polyamide, and wherein the triamine-functionalized polysilicate mesoporous material has a hierarchical structure of MCM-41. The membrane is adapted for use selected from the use group consisting of oil and water separation, water treatment, desalination, and pharmaceutical filtration.

A filtration membrane including a first layer having a triamine-functionalized polysilicate mesoporous material, a second layer including a polysulfone; and a third layer including a polyester terephthalate is described. An orthosilicate group of the triamine-functionalized polysilicate mesoporous material is bonded to a silicon atom of a silicon-containing triamine to form a triamine-functionalized polysilicate backbone, wherein the silicon-containing triamine and one or more tetramines are covalently crosslinked with terephthaloyl chloride to form a polyamide, and wherein the triamine-functionalized polysilicate mesoporous material has a hierarchical structure of MCM-41. The membrane is adapted for use selected from the use group consisting of oil and water separation, water treatment, desalination, and pharmaceutical filtration.

The present disclosure relates to the technical field of film material, and particularly to a polymeric polyphenol-modified polymer film, a preparation method thereof and a metallized polymer film. According to the present disclosure, corona treatment is performed to a surface of a polymer layer, so that a polar modifying liquid can uniformly coat the surface of the polymer layer, thereby forming a modification layer tightly combined with the polymer layer. Thus, the low-polarity polymer layer surface can be imparted with a durable high polarity. Consequently, the polymer layer is capable of being stably and tightly bonded to a material layer with high polarity and high surface tension, such as a metal layer, for a long period of time, effectively broadening the application scenarios for non-polar polymer substrate layers. By controlling the concentrations of the polyphenolic compound and the cross-linking agent in the modifying liquid, the modification layer formed by a cross-linking reaction can have a suitable cross-linking density and an adequate number of hydroxyl groups, thereby further effectively and stably enhancing the long-term polarity and surface tension of the polymer layer. The preparation method is simple and easy to operate, cost-effective, efficient, and easy to scale up.

The present disclosure relates to the technical field of film material, and particularly to a polymeric polyphenol-modified polymer film, a preparation method thereof and a metallized polymer film. According to the present disclosure, corona treatment is performed to a surface of a polymer layer, so that a polar modifying liquid can uniformly coat the surface of the polymer layer, thereby forming a modification layer tightly combined with the polymer layer. Thus, the low-polarity polymer layer surface can be imparted with a durable high polarity. Consequently, the polymer layer is capable of being stably and tightly bonded to a material layer with high polarity and high surface tension, such as a metal layer, for a long period of time, effectively broadening the application scenarios for non-polar polymer substrate layers. By controlling the concentrations of the polyphenolic compound and the cross-linking agent in the modifying liquid, the modification layer formed by a cross-linking reaction can have a suitable cross-linking density and an adequate number of hydroxyl groups, thereby further effectively and stably enhancing the long-term polarity and surface tension of the polymer layer. The preparation method is simple and easy to operate, cost-effective, efficient, and easy to scale up.

The present invention provides a CO.sub.2-photothermal dual-responsive nanoemulsion separation membrane, relating to the field of chemical separation technology. The membrane is woven from fibers with a three-layer structure: (i) a fiber core, (ii) a middle photothermal coating of carbon-based nanomaterials and polyvinyl alcohol, and (iii) an outer CO.sub.2-responsive functional coating synthesized via free radical polymerization of a CO.sub.2-responsive monomer and a hard monomer. The separation membrane has a pore size distribution below 0.1 m. It exhibits excellent photothermal performance, enabling significant temperature increase on the membrane surface within 15 seconds under near-infrared irradiation, thereby achieving a transition from a protonated to a deprotonated state within 1 minute.

The present invention provides a CO.sub.2-photothermal dual-responsive nanoemulsion separation membrane, relating to the field of chemical separation technology. The membrane is woven from fibers with a three-layer structure: (i) a fiber core, (ii) a middle photothermal coating of carbon-based nanomaterials and polyvinyl alcohol, and (iii) an outer CO.sub.2-responsive functional coating synthesized via free radical polymerization of a CO.sub.2-responsive monomer and a hard monomer. The separation membrane has a pore size distribution below 0.1 m. It exhibits excellent photothermal performance, enabling significant temperature increase on the membrane surface within 15 seconds under near-infrared irradiation, thereby achieving a transition from a protonated to a deprotonated state within 1 minute.

The present invention relates to an organic solvent-soluble copolymerized polyester, a composition for forming an ultrafiltration membrane including the same, and a high water-permeability reverse osmosis membrane prepared therefrom. More specifically, the present invention relates to a polyester that has a high solubility in organic solvents at room temperature and thus can be used to produce ultrafiltration membranes at low cost, a composition for forming an ultrafiltration membrane including the same, and a high water-permeability reverse osmosis membrane prepared therefrom, wherein the reverse osmosis membrane has a reduced production cost and high water permeability.

The present invention relates to an organic solvent-soluble copolymerized polyester, a composition for forming an ultrafiltration membrane including the same, and a high water-permeability reverse osmosis membrane prepared therefrom. More specifically, the present invention relates to a polyester that has a high solubility in organic solvents at room temperature and thus can be used to produce ultrafiltration membranes at low cost, a composition for forming an ultrafiltration membrane including the same, and a high water-permeability reverse osmosis membrane prepared therefrom, wherein the reverse osmosis membrane has a reduced production cost and high water permeability.

A composite membrane that includes a polymeric substrate that defines a plurality of pores and a metal organic framework formed within the pores of the substrate. The metal organic framework is formed through interfacial synthesis of an aqueous metal ion and an organic ligand solution within the pores of the substrate. Methods for membrane synthesis are provided that may include a first growth phase and a second growth phase within the pores of the polymeric substrate. The composite membranes may be incorporated into a housing/module for use in gas separation, e.g., in gas separation facilities, including flue gas sorption plants, direct air capture plants, natural gas sweetening pipelines, and olefin/paraffin separation towers.

A composite membrane that includes a polymeric substrate that defines a plurality of pores and a metal organic framework formed within the pores of the substrate. The metal organic framework is formed through interfacial synthesis of an aqueous metal ion and an organic ligand solution within the pores of the substrate. Methods for membrane synthesis are provided that may include a first growth phase and a second growth phase within the pores of the polymeric substrate. The composite membranes may be incorporated into a housing/module for use in gas separation, e.g., in gas separation facilities, including flue gas sorption plants, direct air capture plants, natural gas sweetening pipelines, and olefin/paraffin separation towers.