Abstract: The disclosure of the present invention relates to a method for preparing membrane and associated membrane and filter element. The method comprises providing a porous substrate having a plurality of pores; and applying a pre-filler solution to at least partially occupy the pores in the porous substrate. The membrane comprises a porous substrate and a filter layer formed on the porous substrate. The filter element comprises a core tube; and a membrane as prepared and rolled around the core tube.

Abstract: The disclosure of the present invention relates to a method for preparing membrane and associated membrane and filter element. The method comprises providing a porous substrate having a plurality of pores; and applying a pre-filler solution to at least partially occupy the pores in the porous substrate. The membrane comprises a porous substrate and a filter layer formed on the porous substrate. The filter element comprises a core tube; and a membrane as prepared and rolled around the core tube.

Abstract: Disclosed here are semi-permeable cross-linked polyvinyl alcohol (PVA) based membranes that can be used as supports for water purification membranes, and methods for their production. The cross-linked PVA-based membranes are cross-linked with the reaction product of poly-epoxides and —OH groups from the PVA polymers. Methods according to the present disclosure include crosslinking dissolved PVA and dissolved poly-epoxides, casting the cross-linked PVA, and coagulating the cast polymer in a phase immersion precipitation process.

Abstract: The present disclosure describes an additive that may be used in the manufacture of thin-film polyamide composite membranes. Thin-film polyamide composite membranes are used in filtration processes, such as reverse osmosis and nanofiltration. The additive may be an amino-siloxane compound. The amino-siloxane compound includes repeated groups of silicon bonded to oxygen with at least one amine functional group. Optionally, the amino-siloxane compound may also include a hydrophilic group. The additive reacts with an aqueous phase and an organic phase to form a thin polyamide film on a porous substrate.

Abstract: The present disclosure describes an additive that may be used in the manufacture of thin-film polyamide composite membranes. Thin-film polyamide composite membranes are used in filtration processes, such as reverse osmosis and nanofiltration. The additive may be an amino-siloxane compound. The amino-siloxane compound includes repeated groups of silicon bonded to oxygen with at least one amine functional group. Optionally, the amino-siloxane compound may also include a hydrophilic group. The additive reacts with an aqueous phase and an organic phase to form a thin polyamide film on a porous substrate.

Abstract: The present disclosure describes an additive that may be used in the manufacture of thin-film polyamide composite membranes. Thin-film polyamide composite membranes are used in filtration processes, such as reverse osmosis and nanofiltration. The additive may be an amino-siloxane compound. The amino-siloxane compound includes repeated groups of silicon bonded to oxygen with at least one amine functional group. Optionally, the amino-siloxane compound may also include a hydrophilic group. The additive reacts with an aqueous phase and an organic phase to form a thin polyamide film on a porous substrate.

Abstract: The present disclosure describes an additive that may be used in the manufacture of thin-film polyamide composite membranes. Thin-film polyamide composite membranes are used in filtration processes, such as reverse osmosis and nanofiltration. The additive may be an amino-siloxane compound. The amino-siloxane compound includes repeated groups of silicon bonded to oxygen with at least one amine functional group. Optionally, the amino-siloxane compound may also include a hydrophilic group. The additive reacts with an aqueous phase and an organic phase to form a thin polyamide film on a porous substrate.

Abstract: Processes and apparatus are disclosed for producing clear reverse osmosis retentates having silica concentrations which are substantially supersaturated in silica from feedwaters having silica concentrations, without substantial formation of alkali-soluble scale having substantial silica content in the associated reverse osmosis apparatus, by adjusting the pH of such feedwaters to an acidic pH range prior to reverse osmosis in accordance with this invention. Also disclosed are related processes and apparatus for periodically removing minor amounts of alkali-soluble scale having substantial silica content from the apparatus.

Abstract: Processes and apparatus are disclosed for producing clear reverse osmosis retentates having silica concentrations which are substantially supersaturated in silica from feedwaters having silica concentrations, without substantial formation of alkali-soluble scale having substantial silica content in the associated reverse osmosis apparatus, by adjusting the pH of such feedwaters to an acidic pH range prior to reverse osmosis in accordance with this invention. Also disclosed are related processes and apparatus for periodically removing minor amounts of alkali-soluble scale having substantial silica content from the apparatus.

Abstract: The invention pertains to the polymerization of molecules having electrophilic and nucleophilic substituents on the same or different molecules, such polymerization mediated by aminopyridine catalysts which are substantially regenerated during polymerization. The invention also pertains to polymer products of such polymerization, to permselective membranes containing such polymers, and to processes and apparatus for separating fluids.

Abstract: Asymmetric, semipermeable membranes cast from a solution comprised of poly(aryletherketone) dissolved in a strongly protic non-reactive acid.

Abstract: A process is provided for catalytic hydrogenation of glycolaldehyde to form ethylene glycol in liquid phase employing a homogeneous ruthenium catalyst and a basic promoter. Ethylene glycol is produced in excellent yields and selectivities, and the process permits use of mild temperature and pressure conditions.

Abstract: A process is provided for catalytic hydrogenation of glycolaldehyde to form ethylene glycol in liquid phase employing a homogeneous ruthenium carboxylate complex catalyst system. Ethylene glycol is produced in excellent yields and selectivities and the process permits use of mild temperature and pressure conditions. The formation of acetals is greatly minimized as compared to prior art ruthenium catalysts.

Abstract: A process for the catalytic preparation of aryl carboxylates is provided in which an arylmetallo carboxylate is contacted in liquid medium with an organic peracid in the presence of a catalytic amount of an aryl iodide, to form the desired aryl carboxylate.

Abstract: A process for the preparation of aryl carboxylates is provided in which an arylmetallo carboxylate is contacted with an aryliodoso carboxylate in liquid medium to form the desired aryl carboxylate. Promoters can be employed to increase the rate of reaction and improve selectivity to the aryl carboxylate.