DE60021407T2 - Verfahren zur herstellung eines porösen vernetzten polymers - Google Patents
Verfahren zur herstellung eines porösen vernetzten polymers Download PDFInfo
- Publication number
- DE60021407T2 DE60021407T2 DE60021407T DE60021407T DE60021407T2 DE 60021407 T2 DE60021407 T2 DE 60021407T2 DE 60021407 T DE60021407 T DE 60021407T DE 60021407 T DE60021407 T DE 60021407T DE 60021407 T2 DE60021407 T2 DE 60021407T2
- Authority
- DE
- Germany
- Prior art keywords
- hipe
- temperature
- polymerization
- emulsion
- water
- 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.)
- Expired - Lifetime
Links
- 229920006037 cross link polymer Polymers 0.000 title claims description 136
- 238000004519 manufacturing process Methods 0.000 title description 26
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 179
- 238000006116 polymerization reaction Methods 0.000 claims description 178
- 239000003505 polymerization initiator Substances 0.000 claims description 125
- 238000000034 method Methods 0.000 claims description 108
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- 239000000178 monomer Substances 0.000 claims description 85
- 230000000379 polymerizing effect Effects 0.000 claims description 43
- 230000015572 biosynthetic process Effects 0.000 claims description 41
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- -1 acrylic ester Chemical class 0.000 description 39
- NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 description 26
- 238000000926 separation method Methods 0.000 description 25
- 238000000354 decomposition reaction Methods 0.000 description 21
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- VBICKXHEKHSIBG-UHFFFAOYSA-N 1-monostearoylglycerol Chemical compound CCCCCCCCCCCCCCCCCC(=O)OCC(O)CO VBICKXHEKHSIBG-UHFFFAOYSA-N 0.000 description 4
- YKTNISGZEGZHIS-UHFFFAOYSA-N 2-$l^{1}-oxidanyloxy-2-methylpropane Chemical group CC(C)(C)O[O] YKTNISGZEGZHIS-UHFFFAOYSA-N 0.000 description 4
- LCPVQAHEFVXVKT-UHFFFAOYSA-N 2-(2,4-difluorophenoxy)pyridin-3-amine Chemical compound NC1=CC=CN=C1OC1=CC=C(F)C=C1F LCPVQAHEFVXVKT-UHFFFAOYSA-N 0.000 description 4
- OBETXYAYXDNJHR-UHFFFAOYSA-N 2-Ethylhexanoic acid Chemical compound CCCCC(CC)C(O)=O OBETXYAYXDNJHR-UHFFFAOYSA-N 0.000 description 4
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- 229910001870 ammonium persulfate Inorganic materials 0.000 description 4
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- SHZIWNPUGXLXDT-UHFFFAOYSA-N caproic acid ethyl ester Natural products CCCCCC(=O)OCC SHZIWNPUGXLXDT-UHFFFAOYSA-N 0.000 description 4
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- TXBCBTDQIULDIA-UHFFFAOYSA-N 2-[[3-hydroxy-2,2-bis(hydroxymethyl)propoxy]methyl]-2-(hydroxymethyl)propane-1,3-diol Chemical compound OCC(CO)(CO)COCC(CO)(CO)CO TXBCBTDQIULDIA-UHFFFAOYSA-N 0.000 description 3
- WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 description 3
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- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 3
- 230000000996 additive effect Effects 0.000 description 3
- 239000003093 cationic surfactant Substances 0.000 description 3
- 230000000052 comparative effect Effects 0.000 description 3
- MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 3
- RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Substances CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 3
- 239000006260 foam Substances 0.000 description 3
- 239000000843 powder Substances 0.000 description 3
- KAKZBPTYRLMSJV-UHFFFAOYSA-N vinyl-ethylene Natural products C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 description 3
- 239000011800 void material Substances 0.000 description 3
- 235000013618 yogurt Nutrition 0.000 description 3
- PUPZLCDOIYMWBV-UHFFFAOYSA-N (+/-)-1,3-Butanediol Chemical compound CC(O)CCO PUPZLCDOIYMWBV-UHFFFAOYSA-N 0.000 description 2
- FVQMJJQUGGVLEP-UHFFFAOYSA-N (2-methylpropan-2-yl)oxy 2-ethylhexaneperoxoate Chemical compound CCCCC(CC)C(=O)OOOC(C)(C)C FVQMJJQUGGVLEP-UHFFFAOYSA-N 0.000 description 2
- NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 description 2
- CIWBSHSKHKDKBQ-JLAZNSOCSA-N Ascorbic acid Chemical compound OC[C@H](O)[C@H]1OC(=O)C(O)=C1O CIWBSHSKHKDKBQ-JLAZNSOCSA-N 0.000 description 2
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 2
- FBPFZTCFMRRESA-FSIIMWSLSA-N D-Glucitol Natural products OC[C@H](O)[C@H](O)[C@@H](O)[C@H](O)CO FBPFZTCFMRRESA-FSIIMWSLSA-N 0.000 description 2
- WQZGKKKJIJFFOK-GASJEMHNSA-N Glucose Natural products OC[C@H]1OC(O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-GASJEMHNSA-N 0.000 description 2
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerol Natural products OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 2
- QIGBRXMKCJKVMJ-UHFFFAOYSA-N Hydroquinone Chemical compound OC1=CC=C(O)C=C1 QIGBRXMKCJKVMJ-UHFFFAOYSA-N 0.000 description 2
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 2
- RRHGJUQNOFWUDK-UHFFFAOYSA-N Isoprene Chemical compound CC(=C)C=C RRHGJUQNOFWUDK-UHFFFAOYSA-N 0.000 description 2
- CSNNHWWHGAXBCP-UHFFFAOYSA-L Magnesium sulfate Chemical compound [Mg+2].[O-][S+2]([O-])([O-])[O-] CSNNHWWHGAXBCP-UHFFFAOYSA-L 0.000 description 2
- 239000004698 Polyethylene Substances 0.000 description 2
- PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 2
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 2
- IYFATESGLOUGBX-YVNJGZBMSA-N Sorbitan monopalmitate Chemical compound CCCCCCCCCCCCCCCC(=O)OC[C@@H](O)[C@H]1OC[C@H](O)[C@H]1O IYFATESGLOUGBX-YVNJGZBMSA-N 0.000 description 2
- 239000004147 Sorbitan trioleate Substances 0.000 description 2
- PRXRUNOAOLTIEF-ADSICKODSA-N Sorbitan trioleate Chemical compound CCCCCCCC\C=C/CCCCCCCC(=O)OC[C@@H](OC(=O)CCCCCCC\C=C/CCCCCCCC)[C@H]1OC[C@H](O)[C@H]1OC(=O)CCCCCCC\C=C/CCCCCCCC PRXRUNOAOLTIEF-ADSICKODSA-N 0.000 description 2
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 2
- ZJCCRDAZUWHFQH-UHFFFAOYSA-N Trimethylolpropane Chemical compound CCC(CO)(CO)CO ZJCCRDAZUWHFQH-UHFFFAOYSA-N 0.000 description 2
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- YRKCREAYFQTBPV-UHFFFAOYSA-N acetylacetone Chemical compound CC(=O)CC(C)=O YRKCREAYFQTBPV-UHFFFAOYSA-N 0.000 description 2
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- MPMBRWOOISTHJV-UHFFFAOYSA-N but-1-enylbenzene Chemical compound CCC=CC1=CC=CC=C1 MPMBRWOOISTHJV-UHFFFAOYSA-N 0.000 description 2
- WERYXYBDKMZEQL-UHFFFAOYSA-N butane-1,4-diol Chemical compound OCCCCO WERYXYBDKMZEQL-UHFFFAOYSA-N 0.000 description 2
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- 229910052757 nitrogen Inorganic materials 0.000 description 2
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- 229910052760 oxygen Inorganic materials 0.000 description 2
- WXZMFSXDPGVJKK-UHFFFAOYSA-N pentaerythritol Chemical compound OCC(CO)(CO)CO WXZMFSXDPGVJKK-UHFFFAOYSA-N 0.000 description 2
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- CUNWUEBNSZSNRX-RKGWDQTMSA-N (2r,3r,4r,5s)-hexane-1,2,3,4,5,6-hexol;(z)-octadec-9-enoic acid Chemical compound OC[C@H](O)[C@@H](O)[C@H](O)[C@H](O)CO.OC[C@H](O)[C@@H](O)[C@H](O)[C@H](O)CO.CCCCCCCC\C=C/CCCCCCCC(O)=O.CCCCCCCC\C=C/CCCCCCCC(O)=O.CCCCCCCC\C=C/CCCCCCCC(O)=O CUNWUEBNSZSNRX-RKGWDQTMSA-N 0.000 description 1
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- 238000011084 recovery Methods 0.000 description 1
- 230000002787 reinforcement Effects 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- 230000000717 retained effect Effects 0.000 description 1
- 230000002441 reversible effect Effects 0.000 description 1
- 238000012552 review Methods 0.000 description 1
- 238000007789 sealing Methods 0.000 description 1
- 239000003566 sealing material Substances 0.000 description 1
- 238000009751 slip forming Methods 0.000 description 1
- 239000011780 sodium chloride Substances 0.000 description 1
- JVBXVOWTABLYPX-UHFFFAOYSA-L sodium dithionite Chemical compound [Na+].[Na+].[O-]S(=O)S([O-])=O JVBXVOWTABLYPX-UHFFFAOYSA-L 0.000 description 1
- 229940079827 sodium hydrogen sulfite Drugs 0.000 description 1
- 235000010267 sodium hydrogen sulphite Nutrition 0.000 description 1
- 229940045872 sodium percarbonate Drugs 0.000 description 1
- AKHNMLFCWUSKQB-UHFFFAOYSA-L sodium thiosulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=S AKHNMLFCWUSKQB-UHFFFAOYSA-L 0.000 description 1
- 235000019345 sodium thiosulphate Nutrition 0.000 description 1
- SPDUKHLMYVCLOA-UHFFFAOYSA-M sodium;ethaneperoxoate Chemical compound [Na+].CC(=O)O[O-] SPDUKHLMYVCLOA-UHFFFAOYSA-M 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 229940035044 sorbitan monolaurate Drugs 0.000 description 1
- 239000001587 sorbitan monostearate Substances 0.000 description 1
- 235000011076 sorbitan monostearate Nutrition 0.000 description 1
- 229940035048 sorbitan monostearate Drugs 0.000 description 1
- 229960005078 sorbitan sesquioleate Drugs 0.000 description 1
- 239000001589 sorbitan tristearate Substances 0.000 description 1
- 235000011078 sorbitan tristearate Nutrition 0.000 description 1
- 229960004129 sorbitan tristearate Drugs 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- 230000003068 static effect Effects 0.000 description 1
- 125000004079 stearyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 229910052717 sulfur Inorganic materials 0.000 description 1
- 239000011593 sulfur Substances 0.000 description 1
- 150000003467 sulfuric acid derivatives Chemical class 0.000 description 1
- 239000008399 tap water Substances 0.000 description 1
- 235000020679 tap water Nutrition 0.000 description 1
- WYKYCHHWIJXDAO-UHFFFAOYSA-N tert-butyl 2-ethylhexaneperoxoate Chemical compound CCCCC(CC)C(=O)OOC(C)(C)C WYKYCHHWIJXDAO-UHFFFAOYSA-N 0.000 description 1
- GSECCTDWEGTEBD-UHFFFAOYSA-N tert-butylperoxycyclohexane Chemical compound CC(C)(C)OOC1CCCCC1 GSECCTDWEGTEBD-UHFFFAOYSA-N 0.000 description 1
- 238000012360 testing method Methods 0.000 description 1
- 238000005979 thermal decomposition reaction Methods 0.000 description 1
- 238000012719 thermal polymerization Methods 0.000 description 1
- VPYJNCGUESNPMV-UHFFFAOYSA-N triallylamine Chemical compound C=CCN(CC=C)CC=C VPYJNCGUESNPMV-UHFFFAOYSA-N 0.000 description 1
- ZIBGPFATKBEMQZ-UHFFFAOYSA-N triethylene glycol Chemical compound OCCOCCOCCO ZIBGPFATKBEMQZ-UHFFFAOYSA-N 0.000 description 1
- 238000009281 ultraviolet germicidal irradiation Methods 0.000 description 1
- 210000002700 urine Anatomy 0.000 description 1
- 239000003981 vehicle Substances 0.000 description 1
- 239000007762 w/o emulsion Substances 0.000 description 1
- 238000010792 warming Methods 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
- 239000002699 waste material Substances 0.000 description 1
- 238000004065 wastewater treatment Methods 0.000 description 1
- 229920003169 water-soluble polymer Polymers 0.000 description 1
- 238000005303 weighing Methods 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J9/00—Working-up of macromolecular substances to porous or cellular articles or materials; After-treatment thereof
- C08J9/28—Working-up of macromolecular substances to porous or cellular articles or materials; After-treatment thereof by elimination of a liquid phase from a macromolecular composition or article, e.g. drying of coagulum
- C08J9/283—Working-up of macromolecular substances to porous or cellular articles or materials; After-treatment thereof by elimination of a liquid phase from a macromolecular composition or article, e.g. drying of coagulum a discontinuous liquid phase emulsified in a continuous macromolecular phase
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F2/00—Processes of polymerisation
- C08F2/32—Polymerisation in water-in-oil emulsions
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J2201/00—Foams characterised by the foaming process
- C08J2201/02—Foams characterised by the foaming process characterised by mechanical pre- or post-treatments
- C08J2201/028—Foaming by preparing of a high internal phase emulsion
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Polymerisation Methods In General (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP29014199 | 1999-10-12 | ||
| JP29014199 | 1999-10-12 | ||
| PCT/JP2000/007070 WO2001027164A1 (en) | 1999-10-12 | 2000-10-12 | Method for production of porous cross-linked polymer |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| DE60021407D1 DE60021407D1 (de) | 2005-08-25 |
| DE60021407T2 true DE60021407T2 (de) | 2006-05-24 |
Family
ID=17752326
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DE60021407T Expired - Lifetime DE60021407T2 (de) | 1999-10-12 | 2000-10-12 | Verfahren zur herstellung eines porösen vernetzten polymers |
Country Status (7)
| Country | Link |
|---|---|
| US (1) | US6395792B1 (https=) |
| EP (1) | EP1228102B1 (https=) |
| JP (1) | JP5069833B2 (https=) |
| AU (1) | AU7684300A (https=) |
| DE (1) | DE60021407T2 (https=) |
| PL (1) | PL199269B1 (https=) |
| WO (1) | WO2001027164A1 (https=) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US11433359B1 (en) | 2018-01-29 | 2022-09-06 | Arrowhead Center, Inc. | Antimicrobial filtration membranes |
Families Citing this family (18)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US6573305B1 (en) * | 1999-09-17 | 2003-06-03 | 3M Innovative Properties Company | Foams made by photopolymerization of emulsions |
| JP4749531B2 (ja) * | 2000-07-05 | 2011-08-17 | 株式会社日本触媒 | 多孔質重合体の製造方法 |
| US6365642B1 (en) | 2000-10-10 | 2002-04-02 | The Procter & Gamble Company | Rapid preparation of foam materials from high internal phase emulsions |
| US7376064B2 (en) * | 2002-02-25 | 2008-05-20 | Samsung Electronics Co., Ltd. | Method and apparatus for recording data on optical recording medium |
| JP4579286B2 (ja) * | 2004-03-02 | 2010-11-10 | ザ プロクター アンド ギャンブル カンパニー | 高内相エマルションからの発泡体材料の調製 |
| US20070085235A1 (en) * | 2005-10-18 | 2007-04-19 | Boyle Timothy J | Method and apparatus for continuously preparing crosslinked, solution-cast polymer film |
| CA2621457A1 (en) * | 2005-10-19 | 2007-04-26 | Monosol, Llc | Method and apparatus for continuously preparing crosslinked, solution-cast polymer film |
| US20070085234A1 (en) * | 2005-10-19 | 2007-04-19 | Boyle Timothy J | Method and apparatus for solution casting film with secondary component |
| JP2009084429A (ja) * | 2007-09-28 | 2009-04-23 | Fujifilm Corp | フィルム及びその製造方法 |
| KR101651675B1 (ko) | 2009-10-30 | 2016-08-29 | 유한킴벌리 주식회사 | 환형의 흡수부재를 구비하는 흡수제품 |
| US8257787B2 (en) * | 2009-12-30 | 2012-09-04 | The Procter & Gamble Company | Method of using a carrier sheet in a continuous high internal phase emulsion foam forming process |
| US9649233B2 (en) | 2012-04-25 | 2017-05-16 | Kimberly-Clark Worldwide, Inc. | Absorbent personal care articles having longitudinally oriented layers in discrete portions |
| WO2014085974A1 (en) | 2012-12-04 | 2014-06-12 | Kimberly-Clark Worldwide, Inc. | An absorbent article with a multi-layered topsheet |
| EP3744773B1 (en) | 2018-01-23 | 2022-04-13 | FUJIFILM Corporation | Method for producing porous molded article |
| WO2019146557A1 (ja) * | 2018-01-23 | 2019-08-01 | 富士フイルム株式会社 | 成形材料 |
| WO2019146558A1 (ja) * | 2018-01-23 | 2019-08-01 | 富士フイルム株式会社 | 多孔成形体 |
| IT201900017309A1 (it) * | 2019-09-26 | 2021-03-26 | P4P S R L | Materiali polimerici a struttura interna porosa e interconnessa a base di monomeri acrilici ottenuti tramite tecnica dell’emulsione ad elevata quantità di fase interna polimerizzati tramite UV e relativi processi di produzione |
| US20210039066A1 (en) * | 2020-10-29 | 2021-02-11 | Chin-San Hsieh | Process of making substrate with activated carbon |
Family Cites Families (11)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| NZ199916A (en) | 1981-03-11 | 1985-07-12 | Unilever Plc | Low density polymeric block material for use as carrier for included liquids |
| ZA821586B (en) | 1981-03-11 | 1983-10-26 | Unilever Plc | Low density porous cross-linked polymeric materials and their preparation and use as carriers for included liquids |
| DE3208369A1 (de) * | 1982-03-09 | 1983-09-22 | Röhm GmbH, 6100 Darmstadt | Verfahren zur herstellung einer w/oe-emulsion eines wasserloeslichen polymerisats |
| GB8607535D0 (en) | 1986-03-26 | 1986-04-30 | Unilever Plc | Elastic cross-linked polymeric materials |
| US5252619A (en) | 1992-05-29 | 1993-10-12 | Shell Oil Company | Process for preparing low density porous crosslinked polymeric materials |
| US5189070A (en) | 1992-05-29 | 1993-02-23 | Shell Oil Company | Process for preparing low density porous crosslinked polymeric materials |
| US5210104A (en) | 1992-10-15 | 1993-05-11 | Shell Oil Company | Process for preparing low density porous crosslinked polymeric materials |
| US5670101A (en) * | 1996-01-26 | 1997-09-23 | Shell Oil Company | Process to prepare foams from high internal phase emulsions |
| US6187828B1 (en) * | 1998-11-24 | 2001-02-13 | Basf Corporation | Continuous process for manufacturing superabsorbent polymer |
| US6204298B1 (en) * | 1999-02-22 | 2001-03-20 | The Procter & Gamble Company | Processes for the rapid preparation of foam materials from high internal phase emulsions at high temperatures and pressures |
| WO2001018065A1 (en) * | 1999-09-08 | 2001-03-15 | Nippon Shokubai Co., Ltd. | Process for producing porous crosslinked polymer |
-
2000
- 2000-10-12 WO PCT/JP2000/007070 patent/WO2001027164A1/en not_active Ceased
- 2000-10-12 AU AU76843/00A patent/AU7684300A/en not_active Abandoned
- 2000-10-12 US US09/689,350 patent/US6395792B1/en not_active Expired - Lifetime
- 2000-10-12 JP JP2001530382A patent/JP5069833B2/ja not_active Expired - Lifetime
- 2000-10-12 DE DE60021407T patent/DE60021407T2/de not_active Expired - Lifetime
- 2000-10-12 PL PL354601A patent/PL199269B1/pl unknown
- 2000-10-12 EP EP00966429A patent/EP1228102B1/en not_active Expired - Lifetime
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US11433359B1 (en) | 2018-01-29 | 2022-09-06 | Arrowhead Center, Inc. | Antimicrobial filtration membranes |
| US12017187B2 (en) | 2018-01-29 | 2024-06-25 | Arrowhead Center, Inc. | Antimicrobial filtration membranes |
Also Published As
| Publication number | Publication date |
|---|---|
| JP5069833B2 (ja) | 2012-11-07 |
| EP1228102B1 (en) | 2005-07-20 |
| PL354601A1 (en) | 2004-01-26 |
| US6395792B1 (en) | 2002-05-28 |
| EP1228102A1 (en) | 2002-08-07 |
| JP2003511521A (ja) | 2003-03-25 |
| WO2001027164A1 (en) | 2001-04-19 |
| PL199269B1 (pl) | 2008-09-30 |
| AU7684300A (en) | 2001-04-23 |
| DE60021407D1 (de) | 2005-08-25 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| 8364 | No opposition during term of opposition |