Patent classifications
B01D67/00165
POROUS POLY (CYCLIC OLEFIN) MEMBRANES
The disclosure provides certain porous membranes comprised of cyclic polyolefin polymers, such as poly(norbornene)s. In one embodiment, a poly(norbornene) polymer is dissolved in tetrahydrofuran, cast into a film and subjected to solvent induced phase separation to provide a porous filter membrane (i.e., film).
METHOD FOR PREPARING DURABLY HYDROPHILIC AND UNIFORM-PORE ULTRAFILTRATION MEMBRANE
A method for preparing a durably hydrophilic and uniform-pore ultrafiltration membrane is disclosed herein. Chemical reactions between the functional groups and the active bonds of the molecular chains in the membrane materials are initiated perform the grafting of hydrophilic chains on the polymer chains under conventional dissolution conditions of the polymer membrane material (dissolution with synchronized hydrophilization), so as to realize durable hydrophilization of the membrane materials. The resulting hydrophilized polymer solution (a nascent-state membrane) is introduced into a coagulation bath to initiate a crosslinking reaction among the hydrophilic chains. The resulting crosslinking serves to synergistically regulate subsequent phase separation and membrane formation (phase separation under synergistic crosslinking).
METHOD FOR PRODUCING A POLYELECTROLYTE COMPLEX MEMBRANE
The present invention relates to a method for producing a polyelectrolyte complex (PEC) membrane having a predetermined porosity via salt dilution induced phase separation, in which a liquid polymer solution (P) containing polyanions (A) and polycations (C) dissolved in an aqueous medium at an overcritical salt concentration is exposed to an aqueous medium.
Method for preparing aromatic polyamide porous membrane and aromatic polyamide porous membrane prepared thereby
The present invention provides a method for preparing an aromatic polyamide porous membrane and an aromatic polyamide porous membrane prepared by the above method. The method for preparing an aromatic polyamide porous membrane includes the following steps: mixing an ionic liquid with an aromatic polyamide into a solvent to form a mixed solution; the mixed solution forming a membrane in a coagulation bath; and extracting with an extractant to remove the solvent and the ionic liquid from the membrane to yield a porous membrane. In the method of the present invention, the application of the ionic liquid would greatly reduce the application of additives; further, the ionic liquid has a high stability and is easy to be separated from other solvents and be recycled, which assures the safety during the usage and recycle thereof.
NANOFILTRATION MEMBRANE AND MANUFACTURING METHOD
An object of the present invention is to provide a nanofiltration membrane having a molecular weight cut-off of 200 to 1,000 and a high amount pf permeate for methanol, and suitable for use as an organic solvent nanofiltration membrane. A nanofiltration membrane formed using a polyamide resin, the nanofiltration membrane having a molecular weight cut-off of 200 to 1,000 and a methanol permeability of 0.03 L/(m.sup.2.Math.bar.Math.h) or more.
Superhydrophobic polypropylene porous film, preparation method therefor, and method for improving hydrophobicity of polypropylene porous film
A superhydrophobic polypropylene porous film, including a polypropylene porous film substrate, titanium dioxide layers and a surface modifier layer, is disclosed. The titanium dioxide layers are deposited on the surface of the polypropylene porous film substrate by atomic deposition technology; a surface modifier is coated on the titanium dioxide layers; hydrophobic bonds are formed between the titanium dioxide layers and the surface modifier layer; the superhydrophobic polypropylene porous film has a water contact angle greater than 150 degrees, a rolling angle less than 10 degrees, an aperture of 0.1-0.4 μm, a porosity of 50%-80%, a tensile strength of 30-50 MPa, and an elongation at break of 10%-30%. The superhydrophobic polypropylene porous film maintains the chemical resistance, rigidity, and porosity of the polypropylene porous film, and has superhydrophobic properties and a good separation effect after working for 80 hours, thus greatly increasing the service life, and reducing operation costs and working costs in a membrane distillation process.
Superhydrophobic Polypropylene Porous Film, Preparation Method Therefor, and Method for Improving Hydrophobicity of Polypropylene Porous Film
A superhydrophobic polypropylene porous film, including a polypropylene porous film substrate, titanium dioxide layers and a surface modifier layer, is disclosed. The titanium dioxide layers are deposited on the surface of the polypropylene porous film substrate by atomic deposition technology; a surface modifier is coated on the titanium dioxide layers; hydrophobic bonds are formed between the titanium dioxide layers and the surface modifier layer; the superhydrophobic polypropylene porous film has a water contact angle greater than 150 degrees, a rolling angle less than 10 degrees, an aperture of 0.1-0.4 μm, a porosity of 50%-80%, a tensile strength of 30-50 MPa, and an elongation at break of 10%-30%. The superhydrophobic polypropylene porous film maintains the chemical resistance, rigidity, and porosity of the polypropylene porous film, and has superhydrophobic properties and a good separation effect after working for 80 hours, thus greatly increasing the service life, and reducing operation costs and working costs in a membrane distillation process.
Alkali-Stable Nanofiltration Composite Membrane and Method of Manufacture Thereof
Embodiments of the present invention relate to a nanofiltration composite membrane for use to purify water, the methods for preparing said nanofiltration composite membranes and to the nanofiltration composite membranes prepared accordingly.
Hollow Fiber Membrane And Its Preparation Method and Application
This invention discloses a hollow fiber membrane and its preparation method and application, belonging to the field of membrane separation. The preparation method adopts a spinning device with a triple-orifice spinneret, including the casting solution, bore fluid and outer solution. The bore fluid, casting solution and outer solution are respectively co-extruded from the inner, middle and outer orifice of the spinneret, respectively, to form the nascent membrane. The nascent membrane is immersed in external coagulation bath to form a hollow fiber membrane. The outer solution and bore fluid are weakly-polar non-solvents of membrane-forming material and are water soluble. Based on the characteristics of the bore fluid and the outer solution, on the one hand, the mass exchange rate between solvents and non-solvents can be slowed down, the formation of dense skin is effectively avoided, and the surface porosity of the membrane is improved. On the other hand, the liquid film between solvents and non-solvents can finally dissolve in the coagulation bath without remaining in the hollow fiber membrane and spinning device. The hollow fiber membrane is prepared without double dense skins, and the surface porosity of the inner and outer surfaces of the hollow fiber membrane is improved, which is good for the improvement of membrane flux.
MEMBRANES IN THE FORM OF HOLLOW FIBERS FOR THE SEPARATION OF CO2 FROM NATURAL GAS AND METHOD OF PREPARATION BY HEAT TREATMENT AND DEVELOPMENT OF A POLYMERIC MEMBRANE PRECURSOR
The present invention deals with a method for obtaining membranes in the form of hollow fibers with application in the field of carbon dioxide removal from natural gas. The aforementioned membranes are obtained by means of heat treatment of polymeric membranes. In this method, polymeric membranes are obtained by a phase-inversion technique by immersion-precipitation and are subsequently subjected to a heat treatment, that is, that the membranes effectively become precursor membranes of the heat treatment. The heat treatment process involves the optimization of the heating rate, temperature, and stabilization time variables, aiming at the improvement of the transport properties of the polymeric membranes. After the heat treatment, it becomes possible to use the membranes in separation processes of gases which operate at pressures greater than 30 bar, with selectivity for carbon dioxide (CO.sub.2).