ZA200700435B - Polylsulfone-polyether blockcopolymers, process to synthesize it, membranes made therefrom - Google Patents
Polylsulfone-polyether blockcopolymers, process to synthesize it, membranes made therefrom Download PDFInfo
- Publication number
- ZA200700435B ZA200700435B ZA200700435A ZA200700435A ZA200700435B ZA 200700435 B ZA200700435 B ZA 200700435B ZA 200700435 A ZA200700435 A ZA 200700435A ZA 200700435 A ZA200700435 A ZA 200700435A ZA 200700435 B ZA200700435 B ZA 200700435B
- Authority
- ZA
- South Africa
- Prior art keywords
- block
- block copolymer
- phi
- blocks
- copolymer according
- Prior art date
Links
- 229920001400 block copolymer Polymers 0.000 title claims description 45
- 238000000034 method Methods 0.000 title claims description 13
- 239000012528 membrane Substances 0.000 title description 25
- 229920000570 polyether Polymers 0.000 title description 4
- 239000004721 Polyphenylene oxide Substances 0.000 title description 3
- 229920000642 polymer Polymers 0.000 claims description 23
- 125000003118 aryl group Chemical group 0.000 claims description 15
- 229920001577 copolymer Polymers 0.000 claims description 9
- -1 aromatic diol Chemical class 0.000 claims description 7
- 239000002904 solvent Substances 0.000 claims description 6
- IISBACLAFKSPIT-UHFFFAOYSA-N bisphenol A Chemical compound C=1C=C(O)C=CC=1C(C)(C)C1=CC=C(O)C=C1 IISBACLAFKSPIT-UHFFFAOYSA-N 0.000 claims description 5
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 5
- 125000002947 alkylene group Chemical group 0.000 claims description 4
- 239000004615 ingredient Substances 0.000 claims description 4
- 238000006116 polymerization reaction Methods 0.000 claims description 4
- 238000006068 polycondensation reaction Methods 0.000 claims description 3
- VPWNQTHUCYMVMZ-UHFFFAOYSA-N 4,4'-sulfonyldiphenol Chemical compound C1=CC(O)=CC=C1S(=O)(=O)C1=CC=C(O)C=C1 VPWNQTHUCYMVMZ-UHFFFAOYSA-N 0.000 claims description 2
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical group C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 claims description 2
- GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical compound CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 claims description 2
- 238000006073 displacement reaction Methods 0.000 claims description 2
- 229910052736 halogen Inorganic materials 0.000 claims description 2
- 125000005843 halogen group Chemical group 0.000 claims description 2
- 230000000269 nucleophilic effect Effects 0.000 claims description 2
- 230000002194 synthesizing effect Effects 0.000 claims description 2
- 150000002009 diols Chemical class 0.000 claims 2
- ZYZWCJWINLGQRL-UHFFFAOYSA-N 4-phenylcyclohexa-2,4-diene-1,1-diol Chemical group C1=CC(O)(O)CC=C1C1=CC=CC=C1 ZYZWCJWINLGQRL-UHFFFAOYSA-N 0.000 claims 1
- 241000767684 Thoe Species 0.000 claims 1
- 239000007788 liquid Substances 0.000 claims 1
- 230000000063 preceeding effect Effects 0.000 claims 1
- 210000004379 membrane Anatomy 0.000 description 25
- 229920002492 poly(sulfone) Polymers 0.000 description 12
- 229920001223 polyethylene glycol Polymers 0.000 description 8
- 239000002202 Polyethylene glycol Substances 0.000 description 7
- 239000000654 additive Substances 0.000 description 7
- 229920006393 polyether sulfone Polymers 0.000 description 7
- 230000003301 hydrolyzing effect Effects 0.000 description 5
- 230000002209 hydrophobic effect Effects 0.000 description 5
- 239000011148 porous material Substances 0.000 description 5
- ZUOUZKKEUPVFJK-UHFFFAOYSA-N diphenyl Chemical compound C1=CC=CC=C1C1=CC=CC=C1 ZUOUZKKEUPVFJK-UHFFFAOYSA-N 0.000 description 4
- KZTYYGOKRVBIMI-UHFFFAOYSA-N diphenyl sulfone Chemical compound C=1C=CC=CC=1S(=O)(=O)C1=CC=CC=C1 KZTYYGOKRVBIMI-UHFFFAOYSA-N 0.000 description 4
- 229920001477 hydrophilic polymer Polymers 0.000 description 4
- 238000004519 manufacturing process Methods 0.000 description 4
- 238000000108 ultra-filtration Methods 0.000 description 4
- 239000007789 gas Substances 0.000 description 3
- 238000001631 haemodialysis Methods 0.000 description 3
- 230000000322 hemodialysis Effects 0.000 description 3
- 238000001471 micro-filtration Methods 0.000 description 3
- 229920000036 polyvinylpyrrolidone Polymers 0.000 description 3
- 239000001267 polyvinylpyrrolidone Substances 0.000 description 3
- 235000013855 polyvinylpyrrolidone Nutrition 0.000 description 3
- 239000000126 substance Substances 0.000 description 3
- 150000003457 sulfones Chemical class 0.000 description 3
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 2
- 239000005977 Ethylene Substances 0.000 description 2
- QIGBRXMKCJKVMJ-UHFFFAOYSA-N Hydroquinone Chemical compound OC1=CC=C(O)C=C1 QIGBRXMKCJKVMJ-UHFFFAOYSA-N 0.000 description 2
- 241000100287 Membras Species 0.000 description 2
- 230000000996 additive effect Effects 0.000 description 2
- 235000010290 biphenyl Nutrition 0.000 description 2
- 239000004305 biphenyl Substances 0.000 description 2
- VCCBEIPGXKNHFW-UHFFFAOYSA-N biphenyl-4,4'-diol Chemical compound C1=CC(O)=CC=C1C1=CC=C(O)C=C1 VCCBEIPGXKNHFW-UHFFFAOYSA-N 0.000 description 2
- 239000012510 hollow fiber Substances 0.000 description 2
- 229920001515 polyalkylene glycol Polymers 0.000 description 2
- BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Chemical compound [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 description 2
- 230000001954 sterilising effect Effects 0.000 description 2
- 238000004659 sterilization and disinfection Methods 0.000 description 2
- IBRQUKZZBXZOBA-UHFFFAOYSA-N 1-chloro-3-(3-chlorophenyl)sulfonylbenzene Chemical compound ClC1=CC=CC(S(=O)(=O)C=2C=C(Cl)C=CC=2)=C1 IBRQUKZZBXZOBA-UHFFFAOYSA-N 0.000 description 1
- 229930185605 Bisphenol Natural products 0.000 description 1
- BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate Chemical compound [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 0.000 description 1
- WHNWPMSKXPGLAX-UHFFFAOYSA-N N-Vinyl-2-pyrrolidone Chemical compound C=CN1CCCC1=O WHNWPMSKXPGLAX-UHFFFAOYSA-N 0.000 description 1
- 229920012266 Poly(ether sulfone) PES Polymers 0.000 description 1
- 239000004695 Polyether sulfone Substances 0.000 description 1
- 229920000491 Polyphenylsulfone Polymers 0.000 description 1
- 229920003295 Radel® Polymers 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 125000001931 aliphatic group Chemical group 0.000 description 1
- 239000003513 alkali Substances 0.000 description 1
- 238000013459 approach Methods 0.000 description 1
- 229920005601 base polymer Polymers 0.000 description 1
- 235000013405 beer Nutrition 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- ZCILODAAHLISPY-UHFFFAOYSA-N biphenyl ether Natural products C1=C(CC=C)C(O)=CC(OC=2C(=CC(CC=C)=CC=2)O)=C1 ZCILODAAHLISPY-UHFFFAOYSA-N 0.000 description 1
- 125000004432 carbon atom Chemical group C* 0.000 description 1
- 238000005266 casting Methods 0.000 description 1
- 150000001768 cations Chemical class 0.000 description 1
- 239000001913 cellulose Substances 0.000 description 1
- 229920002678 cellulose Polymers 0.000 description 1
- 238000007385 chemical modification Methods 0.000 description 1
- 238000004140 cleaning Methods 0.000 description 1
- 238000003776 cleavage reaction Methods 0.000 description 1
- 238000005345 coagulation Methods 0.000 description 1
- 230000015271 coagulation Effects 0.000 description 1
- 238000000576 coating method Methods 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 229920006351 engineering plastic Polymers 0.000 description 1
- 125000000524 functional group Chemical group 0.000 description 1
- 229920001600 hydrophobic polymer Polymers 0.000 description 1
- 230000005661 hydrophobic surface Effects 0.000 description 1
- 229960004337 hydroquinone Drugs 0.000 description 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
- 230000002427 irreversible effect Effects 0.000 description 1
- 238000002386 leaching Methods 0.000 description 1
- 230000007774 longterm Effects 0.000 description 1
- APVPOHHVBBYQAV-UHFFFAOYSA-N n-(4-aminophenyl)sulfonyloctadecanamide Chemical compound CCCCCCCCCCCCCCCCCC(=O)NS(=O)(=O)C1=CC=C(N)C=C1 APVPOHHVBBYQAV-UHFFFAOYSA-N 0.000 description 1
- 125000004430 oxygen atom Chemical group O* 0.000 description 1
- 230000035699 permeability Effects 0.000 description 1
- 125000000843 phenylene group Chemical group C1(=C(C=CC=C1)*)* 0.000 description 1
- 238000009832 plasma treatment Methods 0.000 description 1
- 229910000027 potassium carbonate Inorganic materials 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 230000002035 prolonged effect Effects 0.000 description 1
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 description 1
- 102000004169 proteins and genes Human genes 0.000 description 1
- 108090000623 proteins and genes Proteins 0.000 description 1
- HNJBEVLQSNELDL-UHFFFAOYSA-N pyrrolidin-2-one Chemical compound O=C1CCCN1 HNJBEVLQSNELDL-UHFFFAOYSA-N 0.000 description 1
- 230000007017 scission Effects 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 238000004513 sizing Methods 0.000 description 1
- 238000001179 sorption measurement Methods 0.000 description 1
- HXJUTPCZVOIRIF-UHFFFAOYSA-N sulfolane Chemical compound O=S1(=O)CCCC1 HXJUTPCZVOIRIF-UHFFFAOYSA-N 0.000 description 1
- 230000001225 therapeutic effect Effects 0.000 description 1
- 238000005690 transetherification reaction Methods 0.000 description 1
- 229920000428 triblock copolymer Polymers 0.000 description 1
- 238000009736 wetting Methods 0.000 description 1
Classifications
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01D—SEPARATION
- B01D71/00—Semi-permeable membranes for separation processes or apparatus characterised by the material; Manufacturing processes specially adapted therefor
- B01D71/06—Organic material
- B01D71/52—Polyethers
- B01D71/521—Aliphatic polyethers
- B01D71/5211—Polyethylene glycol or polyethyleneoxide
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01D—SEPARATION
- B01D71/00—Semi-permeable membranes for separation processes or apparatus characterised by the material; Manufacturing processes specially adapted therefor
- B01D71/06—Organic material
- B01D71/76—Macromolecular material not specifically provided for in a single one of groups B01D71/08 - B01D71/74
- B01D71/80—Block polymers
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G65/00—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule
- C08G65/34—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule from hydroxy compounds or their metallic derivatives
- C08G65/46—Post-polymerisation treatment, e.g. recovery, purification, drying
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01D—SEPARATION
- B01D53/00—Separation of gases or vapours; Recovering vapours of volatile solvents from gases; Chemical or biological purification of waste gases, e.g. engine exhaust gases, smoke, fumes, flue gases, aerosols
- B01D53/22—Separation of gases or vapours; Recovering vapours of volatile solvents from gases; Chemical or biological purification of waste gases, e.g. engine exhaust gases, smoke, fumes, flue gases, aerosols by diffusion
- B01D53/228—Separation of gases or vapours; Recovering vapours of volatile solvents from gases; Chemical or biological purification of waste gases, e.g. engine exhaust gases, smoke, fumes, flue gases, aerosols by diffusion characterised by specific membranes
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01D—SEPARATION
- B01D71/00—Semi-permeable membranes for separation processes or apparatus characterised by the material; Manufacturing processes specially adapted therefor
- B01D71/06—Organic material
- B01D71/66—Polymers having sulfur in the main chain, with or without nitrogen, oxygen or carbon only
- B01D71/68—Polysulfones; Polyethersulfones
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G65/00—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule
- C08G65/02—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule from cyclic ethers by opening of the heterocyclic ring
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G65/00—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule
- C08G65/34—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule from hydroxy compounds or their metallic derivatives
- C08G65/38—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule from hydroxy compounds or their metallic derivatives derived from phenols
- C08G65/40—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule from hydroxy compounds or their metallic derivatives derived from phenols from phenols (I) and other compounds (II), e.g. OH-Ar-OH + X-Ar-X, where X is halogen atom, i.e. leaving group
- C08G65/42—Phenols and polyhydroxy ethers
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G75/00—Macromolecular compounds obtained by reactions forming a linkage containing sulfur with or without nitrogen, oxygen, or carbon in the main chain of the macromolecule
- C08G75/20—Polysulfones
- C08G75/23—Polyethersulfones
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01D—SEPARATION
- B01D71/00—Semi-permeable membranes for separation processes or apparatus characterised by the material; Manufacturing processes specially adapted therefor
- B01D71/06—Organic material
- B01D71/52—Polyethers
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US58984804P | 2004-07-22 | 2004-07-22 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| ZA200700435B true ZA200700435B (en) | 2008-07-30 |
Family
ID=35033551
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ZA200700435A ZA200700435B (en) | 2004-07-22 | 2007-01-15 | Polylsulfone-polyether blockcopolymers, process to synthesize it, membranes made therefrom |
Country Status (9)
| Country | Link |
|---|---|
| EP (1) | EP1773913B1 (ko) |
| JP (1) | JP2008507614A (ko) |
| KR (1) | KR20070036141A (ko) |
| CN (1) | CN1989174A (ko) |
| AT (1) | ATE412686T1 (ko) |
| DE (1) | DE602005010711D1 (ko) |
| SG (1) | SG129009A1 (ko) |
| WO (1) | WO2006012453A1 (ko) |
| ZA (1) | ZA200700435B (ko) |
Families Citing this family (13)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| MY153648A (en) | 2006-06-22 | 2015-03-13 | Basf Se | Polysulphones and polyether sulphones with reduced yellow index and processes for their preparation |
| ES2379436T5 (es) * | 2007-12-18 | 2016-03-29 | Solvay Specialty Polymers Usa, Llc. | Copolímeros de polifenilsulfonacetona |
| KR100950087B1 (ko) * | 2008-04-21 | 2010-03-29 | 한국화학연구원 | 폴리에테르 설폰 수지의 제조방법 |
| BR112013030102A2 (pt) * | 2011-05-25 | 2016-09-20 | Solvay Specialty Polymers Usa | polímeros com atividade estrogênica reduzida |
| US9758634B2 (en) | 2013-05-02 | 2017-09-12 | Basf Se | Polyarylethersulfone copolymers |
| EP3063224A4 (en) * | 2013-11-01 | 2017-06-21 | Virginia Tech Intellectual Properties, Inc. | Crosslinked polymer compositions for gas separation membranes |
| CN106659982B (zh) * | 2014-08-12 | 2020-06-26 | 巴斯夫欧洲公司 | 制备膜的方法 |
| JP6379995B2 (ja) * | 2014-10-24 | 2018-08-29 | Nok株式会社 | 炭素膜用製膜原液およびこれを用いた中空糸炭素膜の製造方法 |
| CN105504299A (zh) * | 2016-02-24 | 2016-04-20 | 中国科学院烟台海岸带研究所 | 一种aba型聚砜家族嵌段共聚物的合成方法 |
| WO2017187279A1 (en) | 2016-04-29 | 2017-11-02 | Sabic Global Technologies B.V. | Healable thermoplastic resins |
| JP7305621B2 (ja) | 2017-09-11 | 2023-07-10 | フレセニウス メディカル ケア ホールディングス インコーポレーテッド | 微多孔膜およびその作製方法 |
| WO2021182342A1 (ja) * | 2020-03-09 | 2021-09-16 | 住友化学株式会社 | ブロックコポリマー |
| WO2024078975A1 (en) | 2022-10-11 | 2024-04-18 | Solvay Specialty Polymers Usa, Llc | Polyarylethersulfone copolymer having improved hydrophilicity |
Family Cites Families (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4625000A (en) * | 1985-06-12 | 1986-11-25 | Union Carbide Corporation | Process for preparing sulfonated poly(aryl ether) resins |
| JPS6375031A (ja) * | 1985-06-12 | 1988-04-05 | アモコ・コ−ポレイション | スルホン化ポリ（アリ−ルエ−テル）樹脂の製造方法 |
| DE19515689A1 (de) * | 1995-04-28 | 1996-10-31 | Bayer Ag | Polysulfon/Polyether-Blockcopolykondensate |
| US5911880A (en) * | 1995-12-15 | 1999-06-15 | Research Corporation Technologies, Inc. | Self-wetting membranes from engineering plastics |
| JP3983337B2 (ja) * | 1996-03-29 | 2007-09-26 | 帝人株式会社 | ポリアルキルエーテル単位を含むスルホンおよびケトンの医療用材料への適用 |
| DE19907605A1 (de) * | 1999-02-23 | 2000-08-24 | Bayer Ag | Verfahren zur Herstellung von Polyetherblockcopolysulfonen |
-
2005
- 2005-07-21 EP EP05773816A patent/EP1773913B1/en not_active Not-in-force
- 2005-07-21 AT AT05773816T patent/ATE412686T1/de not_active IP Right Cessation
- 2005-07-21 DE DE602005010711T patent/DE602005010711D1/de active Active
- 2005-07-21 SG SG200700240A patent/SG129009A1/en unknown
- 2005-07-21 KR KR1020077001371A patent/KR20070036141A/ko not_active Application Discontinuation
- 2005-07-21 WO PCT/US2005/025944 patent/WO2006012453A1/en active Application Filing
- 2005-07-21 JP JP2007522771A patent/JP2008507614A/ja active Pending
- 2005-07-21 CN CNA200580024377XA patent/CN1989174A/zh active Pending
-
2007
- 2007-01-15 ZA ZA200700435A patent/ZA200700435B/en unknown
Also Published As
| Publication number | Publication date |
|---|---|
| JP2008507614A (ja) | 2008-03-13 |
| KR20070036141A (ko) | 2007-04-02 |
| ATE412686T1 (de) | 2008-11-15 |
| EP1773913A1 (en) | 2007-04-18 |
| EP1773913B1 (en) | 2008-10-29 |
| WO2006012453A1 (en) | 2006-02-02 |
| DE602005010711D1 (de) | 2008-12-11 |
| CN1989174A (zh) | 2007-06-27 |
| SG129009A1 (en) | 2007-02-26 |
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