CN1145918A - Method for preparing chlorine-resistant aromatic polyamide reverse osmosis composite membrane by interface control - Google Patents
Method for preparing chlorine-resistant aromatic polyamide reverse osmosis composite membrane by interface control Download PDFInfo
- Publication number
- CN1145918A CN1145918A CN 95116419 CN95116419A CN1145918A CN 1145918 A CN1145918 A CN 1145918A CN 95116419 CN95116419 CN 95116419 CN 95116419 A CN95116419 A CN 95116419A CN 1145918 A CN1145918 A CN 1145918A
- Authority
- CN
- China
- Prior art keywords
- composite membrane
- chlorine
- reverse osmosis
- interface control
- aromatic polyamide
- 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
- 239000012528 membrane Substances 0.000 title claims abstract description 30
- 239000002131 composite material Substances 0.000 title claims abstract description 29
- 229910052801 chlorine Inorganic materials 0.000 title claims abstract description 19
- 239000000460 chlorine Substances 0.000 title claims abstract description 19
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 title claims abstract description 16
- 239000004760 aramid Substances 0.000 title claims abstract description 9
- 229920003235 aromatic polyamide Polymers 0.000 title claims abstract description 9
- 238000001223 reverse osmosis Methods 0.000 title claims abstract description 9
- 238000000034 method Methods 0.000 title claims abstract description 6
- WFDIJRYMOXRFFG-UHFFFAOYSA-N Acetic anhydride Chemical compound CC(=O)OC(C)=O WFDIJRYMOXRFFG-UHFFFAOYSA-N 0.000 claims abstract description 18
- 229920002492 poly(sulfone) Polymers 0.000 claims abstract description 10
- XTHPWXDJESJLNJ-UHFFFAOYSA-N chlorosulfonic acid Substances OS(Cl)(=O)=O XTHPWXDJESJLNJ-UHFFFAOYSA-N 0.000 claims abstract description 9
- 239000004568 cement Substances 0.000 claims description 4
- 150000001875 compounds Chemical class 0.000 claims description 4
- 238000001125 extrusion Methods 0.000 claims description 3
- NGNBDVOYPDDBFK-UHFFFAOYSA-N 2-[2,4-di(pentan-2-yl)phenoxy]acetyl chloride Chemical compound CCCC(C)C1=CC=C(OCC(Cl)=O)C(C(C)CCC)=C1 NGNBDVOYPDDBFK-UHFFFAOYSA-N 0.000 claims 1
- 229920000768 polyamine Polymers 0.000 claims 1
- 238000004132 cross linking Methods 0.000 abstract description 3
- KEQGZUUPPQEDPF-UHFFFAOYSA-N 1,3-dichloro-5,5-dimethylimidazolidine-2,4-dione Chemical compound CC1(C)N(Cl)C(=O)N(Cl)C1=O KEQGZUUPPQEDPF-UHFFFAOYSA-N 0.000 abstract 2
- 239000004952 Polyamide Substances 0.000 abstract 1
- 238000013329 compounding Methods 0.000 abstract 1
- 229920002647 polyamide Polymers 0.000 abstract 1
- 239000007864 aqueous solution Substances 0.000 description 7
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 6
- 239000000243 solution Substances 0.000 description 6
- 238000005660 chlorination reaction Methods 0.000 description 5
- 239000002346 layers by function Substances 0.000 description 5
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 4
- 239000010410 layer Substances 0.000 description 4
- 238000012696 Interfacial polycondensation Methods 0.000 description 3
- IJOOHPMOJXWVHK-UHFFFAOYSA-N chlorotrimethylsilane Chemical compound C[Si](C)(C)Cl IJOOHPMOJXWVHK-UHFFFAOYSA-N 0.000 description 3
- SUKJFIGYRHOWBL-UHFFFAOYSA-N sodium hypochlorite Chemical compound [Na+].Cl[O-] SUKJFIGYRHOWBL-UHFFFAOYSA-N 0.000 description 3
- 239000000126 substance Substances 0.000 description 3
- RUOKPLVTMFHRJE-UHFFFAOYSA-N benzene-1,2,3-triamine Chemical compound NC1=CC=CC(N)=C1N RUOKPLVTMFHRJE-UHFFFAOYSA-N 0.000 description 2
- 239000003795 chemical substances by application Substances 0.000 description 2
- 238000011065 in-situ storage Methods 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- 238000006068 polycondensation reaction Methods 0.000 description 2
- 239000011148 porous material Substances 0.000 description 2
- 239000011780 sodium chloride Substances 0.000 description 2
- 238000012695 Interfacial polymerization Methods 0.000 description 1
- 150000001408 amides Chemical class 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000007654 immersion Methods 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 239000000178 monomer Substances 0.000 description 1
- 238000009832 plasma treatment Methods 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 238000006116 polymerization reaction Methods 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 150000003254 radicals Chemical class 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 125000000020 sulfo group Chemical group O=S(=O)([*])O[H] 0.000 description 1
- 238000006277 sulfonation reaction Methods 0.000 description 1
Landscapes
- Separation Using Semi-Permeable Membranes (AREA)
Abstract
The invention belongs to a method for preparing a chlorine-resistant aromatic polyamide reverse osmosis composite membrane by adopting interface control. Treating polysulfone supporting base membrane with 1-5% acetic anhydride solution of chlorosulfonic acid for 30-300 s, or treating with 10-50W plasma for 2-10h, and compounding with one aromatic polyamide film, wherein the obtained composite membrane is treated at 110 deg.C for 10 min to crosslink polyamide and polysulfone molecules at interface to increase chlorine resistance of the membrane. Crosslinking with chlorosulfonic acid can achieve a chlorine resistance of 3,000ppm.h, and crosslinking with plasma can achieve a chlorine resistance of 25,000 ppm.h.
Description
The invention belongs to and adopt interface control to prepare the method for the aromatic polyamides of anti-chlorine reverse osmosis composite membrane.
Composite membrane is that one deck ultrathin functional layer is deposited to suitable micropore counterdie surface, aperture.Depositional mode mainly contains surface-coated, interfacial polycondensation and polymerization in situ etc.Composite membrane has many advantages than asymmetric membrane: it can make every layer to reach optimum performance by cutting out.Ultrathin functional layer can be optimized to ideal and select perviousness, and counterdie can reach best intensity and pressure tightness, and the two reaches best chemical-resistant stability together.In addition, composite membrane can make the material that is difficult to form asymmetric membrane form ultrathin membrane, as because solvent limitation and crosslinking polymer can form composite membrane by polymerization in situ or interfacial polycondensation.On the polysulfones counterdie, become the composite membrane kind of present over-all properties optimum by the reverse osmosis composite membrane of the compound one deck aromatic polyamides of interfacial polycondensation ultrathin functional layer gained.Because the leading role of ultrathin functional layer on the composite membrane performance, the physical chemistry structure of therefore controlling ultrathin functional layer becomes the focus of people's research.Though obtained many achievements, but some problems are still unresolved: be subjected to great restriction as the raising of the chemical-resistant stability of reverse osmosis composite membrane owing to the structure of superthin layer itself, just thereby limiting the use range of reverse osmosis composite membrane using the short period of time film properties seriously to descend under certain well-oxygenated environment as under the free chlorine condition.Scientists makes the superthin layer molecule produce the crosslinked resistance to chlorine that improves by the chemical structure that changes superthin layer as adopting polyfunctional monomer.Cadotte US Patent4 in 1981,277,344 adopt interface polycondensation compound aromatic polyamides film on the polysulfones counterdie, this film is linking agent with the pyromellitic trimethylsilyl chloride, film after compound is handled through oxychlorination earlier increases resistance to chlorine, this film is through 2, and salt-stopping rate does not have considerable change after the chlorination of 400ppm.h; Uemura etc. were at US Patent 4 in 1988,761, adopting interface polycondensation in 234 is linking agent with equal benzene triamine, the gained composite membrane is 1, the NaCl aqueous solution of 500ppm, 1.5MPa under the pressure, during pH=7.5 behind the 10ppm free chlorine effect 100h its salt-stopping rate reduce to 99.05% from 99.65%, salt-stopping rate descends 0.6% in 1000ppm.h.Though the over-all properties of Umeura film is better, its used equal this important source material of benzene triamine is difficult to obtain.
The purpose of this invention is to provide and a kind ofly polysulfones is supported the treated reactive group of introducing on the surface of counterdie make the interface of composite membrane produce crosslinked and improve the preparation method of the chlorine-resistant property of aromatic polyamides reverse osmosis composite membrane.
The polysulfones that the present invention adopts phase inversion process to make mean pore size 30nm supports counterdie, then counterdie is handled 30-300 second with the solution of acetic anhydride of the chlorsulfonic acid of 1-5% or with the Cement Composite Treated by Plasma 2-10h of 10-50W power, the counterdie of handling is immersed in contains in 2.0% the mphenylenediamine aqueous solution 7 minutes, with reaction in the hexane solution that is immersed in 0.15% pyromellitic trimethylsilyl chloride behind the rubber roll roll extrusion counterdie surface 20 seconds, in 110 ℃ baking oven, handled 10 minutes.Because thereby the reactive behavior of sulfo group and free radical makes at the interface polymeric amide molecule and the crosslinked chlorine-resistant property that increases film of the intermolecular generation of polysulfones.The gained composite membrane is 5, and the NaCl aqueous solution of 000ppm and the NaClO aqueous solution of 100ppm, the pressure of 1.5MPa are surveyed its chlorine-resistant property down.Reach 3 with the crosslinked resistance to chlorine of film that makes of chlorsulfonic acid, 000ppm.h reaches 25,000ppm.h with the crosslinked chlorine-resistant property of film that makes of plasma body.
Embodiment provided by the invention is as follows:
Embodiment 1. adopts the solution of acetic anhydride of 3% chlorsulfonic acid to carry out surperficial heterogeneous sulfonation 40 seconds the polysulfones counterdie of mean pore size 30nm, then its immersion is contained in the aqueous solution of 2.0% mphenylenediamine 7 minutes, be immersed in the hexane solution 20 seconds that contains 0.15% pyromellitic trimethylsilyl chloride after half-dried with rubber roll roll extrusion counterdie surface, take out the baking oven of putting into 110 ℃ and handled 10 minutes.Gained composite membrane salt-stopping rate is 98.4%, and film is immersed in pH=8, and its salt-stopping rate is 98.1% behind the NaClO aqueous solution 30h of 100ppm, and 3, salt-stopping rate descends 0.3% in the 000ppm.h.
Embodiment 2. counterdies are with example 1, and the solution of acetic anhydride of the chlorsulfonic acid with 1% was handled 150 seconds, and other condition is with example 1, and the salt-stopping rate of gained composite membrane is 97.7%, and through 3, after the chlorination of 000ppm.h, salt-stopping rate is 97.5%.
Embodiment 3. counterdies are with example 1, and the solution of acetic anhydride of the chlorsulfonic acid with 1% was handled 300 seconds, and other condition is with example 1, and the salt-stopping rate of gained composite membrane is 96.2, and through 3, salt-stopping rate is 96.1% after the chlorination of 000ppm.h.
Embodiment 4. counterdies are with example 1, and with the Cement Composite Treated by Plasma 5h of 30W power, complex liquid is with example 1, and heat-treat condition is with example 1.Gained composite membrane salt-stopping rate 98.2% is immersed in pH=8 with film, in the aqueous solution of 100ppm NaClO behind the 200h its salt-stopping rate be 97.9%, 20, salt-stopping rate descends 0.3% in the 000ppm.h.
Embodiment 5. becomes 50w with the Cement Composite Treated by Plasma power of example 4, and other condition is identical, and the gained composite membrane is through 2, and salt-stopping rate reduces to 98.2% from 98.6% after the 5000ppm.h chlorination.
Embodiment 6. becomes 10h with the plasma treatment time of example 4, and other condition is identical, and the gained composite membrane is through 2, and its salt-stopping rate drops to 97.1% from 97.2% after the chlorination of 5000ppm.h.
Claims (1)
1. an interface control prepares the method for the aromatic polyamides of anti-chlorine reverse osmosis composite membrane, be polysulfones to be supported counterdie directly be immersed in the polyamines solution, with being immersed in the polynary solution of acid chloride behind the rubber roll roll extrusion counterdie surface, it is characterized in that the polysulfones counterdie handled 30-300 second with the solution of acetic anhydride of the chlorsulfonic acid of 1-5% or with the Cement Composite Treated by Plasma 2-10h of 10-50W power, the processing 10 minutes in 110 ℃ baking oven of compound back.Reach 3 with the crosslinked resistance to chlorine of film that makes of chlorsulfonic acid, 000ppm.h reaches 25,000ppm.h with the crosslinked resistance to chlorine of film that makes of plasma body.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CN 95116419 CN1058029C (en) | 1995-09-21 | 1995-09-21 | Method for preparing chlorine-resistant aromatic polyamide reverse osmosis composite membrane by interface control |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CN 95116419 CN1058029C (en) | 1995-09-21 | 1995-09-21 | Method for preparing chlorine-resistant aromatic polyamide reverse osmosis composite membrane by interface control |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| CN1145918A true CN1145918A (en) | 1997-03-26 |
| CN1058029C CN1058029C (en) | 2000-11-01 |
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Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CN 95116419 Expired - Lifetime CN1058029C (en) | 1995-09-21 | 1995-09-21 | Method for preparing chlorine-resistant aromatic polyamide reverse osmosis composite membrane by interface control |
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| Country | Link |
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| CN (1) | CN1058029C (en) |
Cited By (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2008025259A1 (en) * | 2006-08-25 | 2008-03-06 | Vontron Membrane Technology Co., Ltd. | Oxidation-resistant composite reverse osmosis membrane |
| CN100391583C (en) * | 2004-11-18 | 2008-06-04 | 国家海洋局杭州水处理技术研究开发中心 | High-flux and reverse-osmosis composite membrane from eurelon |
| CN102228809A (en) * | 2011-05-31 | 2011-11-02 | 南京帝膜净水材料开发有限公司 | Method for preparing pollution-resisting reverse osmosis polyamide composite membrane |
| CN102274696A (en) * | 2011-05-31 | 2011-12-14 | 南京帝膜净水材料开发有限公司 | Method for preparing polyamide reverse osmosis composite membrane |
| CN113304619A (en) * | 2021-06-09 | 2021-08-27 | 中芯膜(北京)科技有限公司 | Chlorine-resistant composite reverse osmosis membrane and preparation method thereof |
| CN114028959A (en) * | 2021-11-18 | 2022-02-11 | 沃顿科技股份有限公司 | Ultrathin desalination layer reverse osmosis composite membrane and preparation method thereof |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN101130444B (en) * | 2006-08-23 | 2010-12-29 | 贵阳时代汇通膜科技有限公司 | Low-pollution compound reverse osmosis membrane |
-
1995
- 1995-09-21 CN CN 95116419 patent/CN1058029C/en not_active Expired - Lifetime
Cited By (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN100391583C (en) * | 2004-11-18 | 2008-06-04 | 国家海洋局杭州水处理技术研究开发中心 | High-flux and reverse-osmosis composite membrane from eurelon |
| WO2008025259A1 (en) * | 2006-08-25 | 2008-03-06 | Vontron Membrane Technology Co., Ltd. | Oxidation-resistant composite reverse osmosis membrane |
| CN102228809A (en) * | 2011-05-31 | 2011-11-02 | 南京帝膜净水材料开发有限公司 | Method for preparing pollution-resisting reverse osmosis polyamide composite membrane |
| CN102274696A (en) * | 2011-05-31 | 2011-12-14 | 南京帝膜净水材料开发有限公司 | Method for preparing polyamide reverse osmosis composite membrane |
| CN102228809B (en) * | 2011-05-31 | 2013-07-31 | 南京帝膜净水材料开发有限公司 | Method for preparing pollution-resisting reverse osmosis polyamide composite membrane |
| CN113304619A (en) * | 2021-06-09 | 2021-08-27 | 中芯膜(北京)科技有限公司 | Chlorine-resistant composite reverse osmosis membrane and preparation method thereof |
| CN114028959A (en) * | 2021-11-18 | 2022-02-11 | 沃顿科技股份有限公司 | Ultrathin desalination layer reverse osmosis composite membrane and preparation method thereof |
| CN114028959B (en) * | 2021-11-18 | 2022-08-19 | 沃顿科技股份有限公司 | Ultrathin desalination layer reverse osmosis composite membrane and preparation method thereof |
| WO2023087481A1 (en) * | 2021-11-18 | 2023-05-25 | 沃顿科技股份有限公司 | Reverse osmosis composite membrane having ultrathin desalination layer and preparation method therefor |
Also Published As
| Publication number | Publication date |
|---|---|
| CN1058029C (en) | 2000-11-01 |
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Owner name: HUASHENG LANJIN (TIANJIN) FILM TECHNOLOGY CO., LTD Free format text: FORMER OWNER: CHANGCHUN INST. OF APPLIED CHEMISTRY, CHINESE ACADEMY OF SCIENCES Effective date: 20111205 |
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Free format text: CORRECT: ADDRESS; FROM: 130022 CHANGCHUN, JILIN PROVINCE TO: 301700 WUQING, TIANJIN |
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| TR01 | Transfer of patent right |
Effective date of registration: 20111205 Address after: 301700 Tianjin Fuyuan Wuqing Development Zone No. 18 North Road Patentee after: Huasheng LanJin (Tianjin) Membrane Technology Co Ltd Address before: 130022 No. 109 Stalin street, Changchun, Jilin Patentee before: Changchun Institue of Applied Chemistry, Chinese Academy of Sciences |
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Granted publication date: 20001101 |
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