CN111644075A - Application of graphene oxide nanofiltration membrane under high operating pressure - Google Patents
Application of graphene oxide nanofiltration membrane under high operating pressure Download PDFInfo
- Publication number
- CN111644075A CN111644075A CN202010521134.3A CN202010521134A CN111644075A CN 111644075 A CN111644075 A CN 111644075A CN 202010521134 A CN202010521134 A CN 202010521134A CN 111644075 A CN111644075 A CN 111644075A
- Authority
- CN
- China
- Prior art keywords
- membrane
- graphene oxide
- nanofiltration membrane
- dipping
- operating pressure
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Granted
Links
Classifications
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01D—SEPARATION
- B01D69/00—Semi-permeable membranes for separation processes or apparatus characterised by their form, structure or properties; Manufacturing processes specially adapted therefor
- B01D69/10—Supported membranes; Membrane supports
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01D—SEPARATION
- B01D61/00—Processes of separation using semi-permeable membranes, e.g. dialysis, osmosis or ultrafiltration; Apparatus, accessories or auxiliary operations specially adapted therefor
- B01D61/02—Reverse osmosis; Hyperfiltration ; Nanofiltration
- B01D61/027—Nanofiltration
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01D—SEPARATION
- B01D67/00—Processes specially adapted for manufacturing semi-permeable membranes for separation processes or apparatus
- B01D67/0079—Manufacture of membranes comprising organic and inorganic components
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01D—SEPARATION
- B01D69/00—Semi-permeable membranes for separation processes or apparatus characterised by their form, structure or properties; Manufacturing processes specially adapted therefor
- B01D69/10—Supported membranes; Membrane supports
- B01D69/105—Support pretreatment
Landscapes
- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Nanotechnology (AREA)
- Water Supply & Treatment (AREA)
- Inorganic Chemistry (AREA)
- Manufacturing & Machinery (AREA)
- Carbon And Carbon Compounds (AREA)
- Separation Using Semi-Permeable Membranes (AREA)
Abstract
The invention discloses an application of a graphene oxide nanofiltration membrane under high operating pressure, which is characterized in that: carry out the graphite oxide nanofiltration membrane at the operating pressure that is greater than 0.2MPa, the graphite oxide nanofiltration membrane include supporter and separation layer, the supporter be the organic/inorganic hybrid membrane that contains hydrophilic molecular sieve and polymer, the separation layer for amination graphite oxide and acyl chloride compound interfacial polymerization form, just the supporter pass through acyl chloride crosslinking with amination graphite oxide. The application provided by the invention can meet the application requirement of the graphene oxide nanofiltration membrane under high operating pressure, and has higher application potential.
Description
Technical Field
The invention relates to application of a nanofiltration membrane, in particular to application of a graphene oxide nanofiltration membrane under high operating pressure.
Background
The nanofiltration technology is a membrane separation technology separated from the reverse osmosis technology, and is a continuation and development branch of the ultra-low pressure reverse osmosis technology. For a long time in the past, nanofiltration membranes have been referred to as ultra low pressure reverse osmosis membranes or selective reverse osmosis membranes or loose reverse osmosis membranes. Japanese scholars have specifically defined the separation performance of nanofiltration membranes: the membrane with the operation pressure less than or equal to 1.50mPa, the cut-off molecular weight of 200-1000 and the NaCl cut-off rate less than or equal to 90 percent can be regarded as a nanofiltration membrane. At present, the nanofiltration technology has been separated from the reverse osmosis technology, becomes an independent separation technology between the ultrafiltration technology and the reverse osmosis technology, is widely applied to various fields such as seawater desalination, ultrapure water manufacture, food industry, environmental protection and the like, and becomes an important branch in the membrane separation technology.
Graphene oxide, as a new two-dimensional inorganic nano material, has been widely applied in the preparation of functional materials due to its own physicochemical properties. At present, it has become a common technology to apply graphene oxide to a modified membrane material or directly use graphene oxide as a membrane material, for example, graphene oxide is added to an aqueous phase interface to prepare a polyamide membrane, graphene oxide is added to a PVDF membrane casting solution as an additive to prepare a PVDF composite membrane by a blending method, or graphene is fixed on a support by a layer-by-layer self-assembly method to directly serve as a filtration membrane. In the method, for directly using graphene as a nanofiltration membrane, products prepared in the prior art can only be used in a low-pressure range, generally not more than 0.2Mpa, so that the application range of the graphene nanofiltration membrane is limited. In order to improve the application potential of the graphene nanofiltration membrane, a new graphene nanofiltration membrane is urgently needed to improve the above problems.
Disclosure of Invention
The invention aims to solve the problems in the prior art and provides application of a novel graphene oxide nanofiltration membrane under high operating pressure.
The invention provides an application of a graphene oxide nanofiltration membrane under high operating pressure, which is characterized in that: carry out the graphite oxide nanofiltration membrane at the operating pressure that is greater than 0.2MPa, the graphite oxide nanofiltration membrane include supporter and separation layer, the supporter be the organic/inorganic hybrid membrane that contains hydrophilic molecular sieve and polymer, the separation layer for amination graphite oxide and acyl chloride compound interfacial polymerization form, just the supporter pass through acyl chloride crosslinking with amination graphite oxide.
Specifically, the high operating pressure means an operating pressure of 0.2 to 1.5MPa, preferably 0.5 to 1 MPa.
Specifically, the graphene oxide nanofiltration membrane is prepared by a method comprising the following steps:
(1) preparation of support body by blending method
Mixing a polymer, a solvent, an additive and a hydrophilic molecular sieve, stirring, standing, defoaming to form a membrane casting solution, scraping a membrane on a glass sheet, solidifying in a coagulating bath to form a membrane, soaking in deionized water, drying at high temperature, and forming the membrane as a support for later use;
(2) modification of support by acid chlorination
Dipping the surface of the support prepared in the step (1) in an organic solvent containing an aromatic polyacyl chloride compound for 1-4h, removing the surface solution after finishing dipping, and drying at 40-80 ℃;
(3) preparation of graphene oxide nanofiltration membrane
And (3) dipping the modified support body prepared in the step (2) in an amino-modified graphene oxide aqueous solution for 10-20min, dipping the modified support body in an organic phase solution containing aromatic polybasic acyl chloride again, and performing thermal crosslinking at 60-80 ℃ for 10-30min after dipping to obtain the graphene oxide nanofiltration membrane.
Specifically, the polymer is one of polysulfone, polyethersulfone, cellulose acetate, nylon and polyvinylidene fluoride.
Specifically, the hydrophilic molecular sieve is one of NaA, NaY and ZSM-5.
Specifically, the mass ratio of the polymer to the hydrophilic molecular sieve in the step (1) is 2:1-4: 1.
Specifically, the aromatic polybasic acyl chloride compound in the step (2) and the aromatic polybasic acyl chloride in the step (3) are selected from one or more of isophthaloyl dichloride, terephthaloyl dichloride and phthaloyl dichloride, and the aromatic polybasic acyl chloride compound in the step (2) and the aromatic polybasic acyl chloride in the step (3) can be the same or different.
Specifically, the amino-modified graphene is prepared by dehydration condensation reaction of graphene oxide and ethylenediamine.
Compared with the prior art, the graphene oxide nanofiltration membrane prepared by a proper method can meet the application requirement of the graphene oxide nanofiltration membrane under high operating pressure, and particularly, the application strength of the graphene oxide nanofiltration membrane is improved by cross-linking acyl chloride compounds in a transverse and longitudinal mode in an interfacial polymerization mode. Firstly, in the transverse direction, the amino modified graphene oxide is crosslinked into a net through the crosslinking action of an acyl chloride compound, in the longitudinal direction, the amino modified graphene and the support body are crosslinked together through the acyl chloride modification of the support body, the direct bonding force of the separation layer and the support body is improved, the hydroxyl group of the support body is crosslinked with acyl chloride by adding a hydrophilic molecular sieve on the support body, the acyl chloride degree of the support body is improved, and the water flux of the nanofiltration membrane is improved to a certain extent.
Detailed Description
Preparation of aminated graphene used in the following examples/and or comparative examples: mixing graphene oxide and dimethylformamide, carrying out ultrasonic treatment for 2h, adding ethylenediamine and dicyclohexylcarbodiimide, continuing to carry out ultrasonic treatment for 10min, reacting for 24h at 120 ℃, adding ethanol, standing for 12h, filtering and cleaning thick slurry at the bottom, and drying in an oven at 60 ℃ to obtain aminated graphene oxide for later use, wherein the mass ratio of the graphene oxide to the dimethylformamide to the ethylenediamine to the dicyclohexylcarbodiimide is 1:100:150: 25.
Example 1:
(1) preparation of support body by blending method
Mixing PVDF, dimethylacetamide, polyethylene glycol and NaA molecular sieve (the ratio of silicon to aluminum is 1) according to the mass ratio of 10:120:1:3, stirring, standing and defoaming to form a membrane casting solution, scraping a membrane on a glass sheet, placing the glass sheet into water to solidify and form a membrane, soaking the glass sheet in deionized water, drying the glass sheet at a high temperature of 60 ℃, and forming the membrane as a support for later use;
(2) modification of support by acid chlorination
Dipping the surface of the support prepared in the step (1) in n-hexane containing 0.5wt% of isophthaloyl dichloride, wherein the dipping time is 2h, removing the surface solution after the dipping is finished, and drying at 60 ℃;
(3) preparation of graphene oxide nanofiltration membrane
And (3) dipping the modified support body prepared in the step (2) in an amino-modified graphene oxide aqueous solution (0.5 wt%, adjusting the pH to 11 by adopting NaOH), wherein the dipping time is 10min, dipping the modified support body in n-hexane containing 0.2wt% of isophthaloyl dichloride, and after the dipping is finished, performing thermal crosslinking at 80 ℃ for 30min to obtain the graphene oxide nanofiltration membrane.
Example 2
(1) Preparation of support body by blending method
Mixing PVDF, dimethylacetamide, polyethylene glycol and ZSM-5 molecular sieve (the ratio of silicon to aluminum is 40) according to the mass ratio of 10:120:1:3, stirring, standing and defoaming to form a membrane casting solution, scraping a membrane on a glass sheet, placing the glass sheet into water to solidify and form a membrane, soaking the glass sheet into deionized water, drying the glass sheet at a high temperature of 60 ℃, and forming the membrane as a support for later use;
(2) modification of support by acid chlorination
Dipping the surface of the support prepared in the step (1) in n-hexane containing 0.5wt% of isophthaloyl dichloride, wherein the dipping time is 2h, removing the surface solution after the dipping is finished, and drying at 60 ℃;
(3) preparation of graphene oxide nanofiltration membrane
And (3) dipping the modified support body prepared in the step (2) in an amino-modified graphene oxide aqueous solution (0.5 wt%, adjusting the pH to 11 by adopting NaOH), wherein the dipping time is 10min, dipping the modified support body in n-hexane containing 0.2wt% of isophthaloyl dichloride, and after the dipping is finished, performing thermal crosslinking at 80 ℃ for 30min to obtain the graphene oxide nanofiltration membrane.
Example 3
(1) Preparation of support body by blending method
Mixing PVDF, dimethylacetamide, polyethylene glycol and NaY molecular sieve (the ratio of silicon to aluminum is 6) according to the mass ratio of 10:120:1:3, stirring, standing and defoaming to form a membrane casting solution, scraping a membrane on a glass sheet, placing the glass sheet into water to solidify and form a membrane, soaking the glass sheet in deionized water, drying the glass sheet at a high temperature of 60 ℃, and forming the membrane as a support for later use;
(2) modification of support by acid chlorination
Dipping the surface of the support prepared in the step (1) in n-hexane containing 0.5wt% of isophthaloyl dichloride, wherein the dipping time is 2h, removing the surface solution after the dipping is finished, and drying at 60 ℃;
(3) preparation of graphene oxide nanofiltration membrane
And (3) dipping the modified support body prepared in the step (2) in an amino-modified graphene oxide aqueous solution (0.5 wt%, adjusting the pH to 11 by adopting NaOH), wherein the dipping time is 10min, dipping the modified support body in n-hexane containing 0.2wt% of isophthaloyl dichloride, and after the dipping is finished, performing thermal crosslinking at 80 ℃ for 30min to obtain the graphene oxide nanofiltration membrane.
Comparative example 1
(1) Preparation of the support
Mixing PVDF, dimethylacetamide and polyethylene glycol according to a mass ratio of 10:120:1, stirring, standing and defoaming to form a membrane casting solution, scraping a membrane on a glass sheet, placing the glass sheet into water to solidify and form a membrane, soaking the membrane in deionized water, and drying the membrane at a high temperature of 60 ℃ to form a membrane as a support for later use;
(2) preparation of graphene oxide nanofiltration membrane
And (2) dipping the modified support body prepared in the step (1) in an amino-modified graphene oxide aqueous solution (0.5 wt%, adjusting the pH to 11 by adopting NaOH), wherein the dipping time is 10min, dipping the modified support body in n-hexane containing 0.2wt% of isophthaloyl dichloride, and after the dipping is finished, performing thermal crosslinking at 80 ℃ for 30min to obtain the graphene oxide nanofiltration membrane.
Comparative example 2
(1) Preparation of support body by blending method
Mixing PVDF, dimethylacetamide, polyethylene glycol and NaA molecular sieve (the ratio of silicon to aluminum is 1) according to the mass ratio of 10:120:1:3, stirring, standing and defoaming to form a membrane casting solution, scraping a membrane on a glass sheet, placing the glass sheet into water to solidify and form a membrane, soaking the glass sheet in deionized water, drying the glass sheet at a high temperature of 60 ℃, and forming the membrane as a support for later use;
(2) modification of support by acid chlorination
Dipping the surface of the support prepared in the step (1) in n-hexane containing 0.5wt% of isophthaloyl dichloride, wherein the dipping time is 2h, removing the surface solution after the dipping is finished, and drying at 60 ℃;
(3) preparation of graphene oxide nanofiltration membrane
And (3) fixing the modified support body prepared in the step (2) in a suction filtration device, adding an amino modified graphene oxide aqueous solution (0.5 wt%, adding sodium hydroxide to adjust the pH value to 11) into a filter cup, and performing vacuum suction filtration for 10min to form a film.
Comparative example 3
(1) Preparation of the support
Mixing PVDF, dimethylacetamide and polyethylene glycol according to a mass ratio of 10:120:1, stirring, standing and defoaming to form a membrane casting solution, scraping a membrane on a glass sheet, placing the glass sheet into water to solidify and form a membrane, soaking the membrane in deionized water, and drying the membrane at a high temperature of 60 ℃ to form a membrane as a support for later use;
(2) modification of support by acid chlorination
Dipping the surface of the support prepared in the step (1) in n-hexane containing 0.5wt% of isophthaloyl dichloride, wherein the dipping time is 2h, removing the surface solution after the dipping is finished, and drying at 60 ℃;
(3) preparation of graphene oxide nanofiltration membrane
And (3) dipping the modified support body prepared in the step (2) in an amino-modified graphene oxide aqueous solution (0.5 wt%, adjusting the pH to 11 by adopting NaOH), wherein the dipping time is 10min, dipping the modified support body in n-hexane containing 0.2wt% of isophthaloyl dichloride, and after the dipping is finished, performing thermal crosslinking at 80 ℃ for 30min to obtain the graphene oxide nanofiltration membrane.
The nanofiltration membrane samples prepared in examples 1 to 3 and comparative examples 1 to 3 were subjected to 0.8Mpa pure water flux, NaCl and Na2SO4 rejection tests, and the data were measured at two time points of 0 h and 24h, respectively, with the results shown in the following table.
As can be seen from the above table, the nanofiltration membrane sample prepared by the preparation method provided by the invention has the advantages that the membrane performance (including flux and rejection rate) is not reduced basically with the passage of time under high operation pressure, while the comparative sample shows that the membrane performance is reduced seriously, so that the method provided by the invention can realize separation under high operation pressure to a certain extent.
The above description is only for the purpose of illustrating the preferred embodiments of the present invention and should not be taken as limiting the invention, but rather the intention is to cover all modifications, alternatives, and equivalents falling within the spirit and scope of the invention.
Claims (8)
1. The application of the graphene oxide nanofiltration membrane under high operating pressure is characterized in that: carry out the graphite oxide nanofiltration membrane at the operating pressure that is greater than 0.2MPa, the graphite oxide nanofiltration membrane include supporter and separation layer, the supporter be the organic/inorganic hybrid membrane that contains hydrophilic molecular sieve and polymer, the separation layer for amination graphite oxide and acyl chloride compound interfacial polymerization form, just the supporter pass through acyl chloride crosslinking with amination graphite oxide.
2. Use according to claim 1, characterized in that said high operating pressure is an operating pressure of 0.2-1.5MPa, preferably 0.5-1 MPa.
3. The use according to claim 1, wherein the graphene oxide nanofiltration membrane is prepared by a method comprising the following steps:
(1) preparation of support body by blending method
Mixing a polymer, a solvent, an additive and a hydrophilic molecular sieve, stirring, standing, defoaming to form a membrane casting solution, scraping a membrane on a glass sheet, solidifying in a coagulating bath to form a membrane, soaking in deionized water, drying at high temperature, and forming the membrane as a support for later use;
(2) modification of support by acid chlorination
Dipping the surface of the support prepared in the step (1) in an organic solvent containing an aromatic polyacyl chloride compound for 1-4h, removing the surface solution after finishing dipping, and drying at 40-80 ℃;
(3) preparation of graphene oxide nanofiltration membrane
And (3) dipping the modified support body prepared in the step (2) in an amino-modified graphene oxide aqueous solution for 10-20min, dipping the modified support body in an organic phase solution containing aromatic polybasic acyl chloride again, and performing thermal crosslinking at 60-80 ℃ for 10-30min after dipping to obtain the graphene oxide nanofiltration membrane.
4. The use according to claim 3, wherein the polymer is one of polysulfone, polyethersulfone, cellulose acetate, nylon, polyvinylidene fluoride.
5. The use according to claim 3, wherein the hydrophilic molecular sieve is one of NaA, NaY, ZSM-5.
6. Use according to claim 3, characterized in that in step (1) the mass ratio of polymer to hydrophilic molecular sieve is from 2:1 to 4: 1.
7. The use according to claim 3, wherein the aromatic poly-acid chloride compound in step (2) and the aromatic poly-acid chloride in step (3) are selected from one or more of isophthaloyl dichloride, terephthaloyl dichloride and phthaloyl dichloride, and the aromatic poly-acid chloride compound in step (2) and the aromatic poly-acid chloride in step (3) may be the same or different.
8. The use according to claim 3, wherein the amino-modified graphene is prepared by dehydration condensation reaction of graphene oxide and ethylenediamine.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN202010521134.3A CN111644075B (en) | 2020-06-10 | 2020-06-10 | Application of graphene oxide nanofiltration membrane under high operating pressure |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN202010521134.3A CN111644075B (en) | 2020-06-10 | 2020-06-10 | Application of graphene oxide nanofiltration membrane under high operating pressure |
Publications (2)
Publication Number | Publication Date |
---|---|
CN111644075A true CN111644075A (en) | 2020-09-11 |
CN111644075B CN111644075B (en) | 2021-10-15 |
Family
ID=72343495
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CN202010521134.3A Active CN111644075B (en) | 2020-06-10 | 2020-06-10 | Application of graphene oxide nanofiltration membrane under high operating pressure |
Country Status (1)
Country | Link |
---|---|
CN (1) | CN111644075B (en) |
Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4053286A (en) * | 1974-09-23 | 1977-10-11 | Merck & Co., Inc. | Process for the preparation of cephalosporin antibiotics |
CN101254417A (en) * | 2007-12-14 | 2008-09-03 | 浙江大学 | Crosslinked hyperbranched polyalcohol composite nano filter membrance and method of preparing the same |
CN106823842A (en) * | 2017-03-28 | 2017-06-13 | 天津大学 | A kind of preparation method of graphene oxide composite nano filter membrane |
CN106943894A (en) * | 2017-04-21 | 2017-07-14 | 北京师范大学 | High performance ultra filtration composite membrane that a kind of graphene oxide is modified and preparation method thereof |
CN109092087A (en) * | 2018-09-28 | 2018-12-28 | 南京科技职业学院 | A kind of graphene oxide modified polyamide composite nanometer filtering film and preparation method thereof |
-
2020
- 2020-06-10 CN CN202010521134.3A patent/CN111644075B/en active Active
Patent Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4053286A (en) * | 1974-09-23 | 1977-10-11 | Merck & Co., Inc. | Process for the preparation of cephalosporin antibiotics |
CN101254417A (en) * | 2007-12-14 | 2008-09-03 | 浙江大学 | Crosslinked hyperbranched polyalcohol composite nano filter membrance and method of preparing the same |
CN106823842A (en) * | 2017-03-28 | 2017-06-13 | 天津大学 | A kind of preparation method of graphene oxide composite nano filter membrane |
CN106943894A (en) * | 2017-04-21 | 2017-07-14 | 北京师范大学 | High performance ultra filtration composite membrane that a kind of graphene oxide is modified and preparation method thereof |
CN109092087A (en) * | 2018-09-28 | 2018-12-28 | 南京科技职业学院 | A kind of graphene oxide modified polyamide composite nanometer filtering film and preparation method thereof |
Non-Patent Citations (1)
Title |
---|
王进等: "氧化石墨烯/聚哌嗪酰胺复合纳滤膜在染料脱除中的应用研究", 《膜科学与技术》 * |
Also Published As
Publication number | Publication date |
---|---|
CN111644075B (en) | 2021-10-15 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
CN106823842B (en) | Preparation method of graphene oxide composite nanofiltration membrane | |
US11148099B2 (en) | Graphene-based membrane and method of producing the same | |
JP2014521494A (en) | High permeation flow reverse osmosis membrane containing surface-treated zeolite and method for producing the same | |
WO2021128886A1 (en) | Method for preparing nanofiltration membrane and nanofiltration membrane prepared therefrom | |
CN110201544B (en) | High-flux high-selectivity nanofiltration membrane and preparation method thereof | |
CN112191107A (en) | Preparation method of high-flux polytetrafluoroethylene reverse osmosis membrane | |
CN110694492A (en) | Mixed matrix polyamide membrane of ZIF type metal organic framework and preparation method thereof | |
CN112246110B (en) | Double-functional-layer composite reverse osmosis membrane and preparation method thereof | |
CN111686594A (en) | High-flux high-retention composite membrane and preparation method thereof | |
DE102015214896A1 (en) | Membranes and process for their preparation | |
CN112354366B (en) | High-flux composite reverse osmosis membrane and preparation method thereof | |
CN111644071A (en) | Preparation method of graphene oxide nanofiltration membrane suitable for operation under high operating pressure | |
CN111644075B (en) | Application of graphene oxide nanofiltration membrane under high operating pressure | |
KR20070013651A (en) | Preparation method of highly permeable composite polyamide nanofiltration membranes | |
CN109603584B (en) | Preparation method of hydrophilic polyamide reverse osmosis membrane | |
CN108355498B (en) | Negative charge composite nanofiltration membrane and preparation method thereof | |
CN116688777A (en) | Preparation method of polyvinylidene fluoride membrane for constructing high-flux composite nanofiltration membrane | |
CN107158974B (en) | High-strength hydrophilic nanofiltration membrane, preparation method thereof and application thereof in protein solution desalination process | |
KR102169137B1 (en) | A polyamide composite membrane having improved salt and boron rejection and method for preparation thereof | |
CN113477100A (en) | Seawater desalination nanofiltration membrane and preparation method thereof | |
KR100322235B1 (en) | Fabrication of high permeable reverse osmosis membranes | |
CN111085117B (en) | High-water-permeability reverse osmosis membrane and preparation method thereof | |
CN113856482A (en) | Method for preparing polyamide reverse osmosis membrane with low volume density | |
KR102067861B1 (en) | Composition for preparing reverse osmosis membrane, method for preparing reverse osmosis membrane using the same, and reverse osmosis membrane and water treatment module | |
CN111054214A (en) | Preparation method of composite reverse osmosis membrane |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
PB01 | Publication | ||
PB01 | Publication | ||
SE01 | Entry into force of request for substantive examination | ||
SE01 | Entry into force of request for substantive examination | ||
TA01 | Transfer of patent application right |
Effective date of registration: 20210926 Address after: 325600 Tian Long Village, Qingjiang Town, Yueqing City, Wenzhou, Zhejiang Applicant after: Zhuang Xiuping Address before: 266000 room 223, 2nd floor, building 2, 20 Shanghai Road, Qianwan bonded port area, Qingdao, Shandong Province (high tech Industry Center) Applicant before: Qingdao senchen Environmental Protection Technology Co.,Ltd. |
|
TA01 | Transfer of patent application right | ||
GR01 | Patent grant | ||
GR01 | Patent grant |