BRPI0707065B1 - uso de uma associação de polímeros, método de tratamento de superfície de um material sólido, material sólido de superfície modificada e associações de polímeros - Google Patents
uso de uma associação de polímeros, método de tratamento de superfície de um material sólido, material sólido de superfície modificada e associações de polímeros Download PDFInfo
- Publication number
- BRPI0707065B1 BRPI0707065B1 BRPI0707065A BRPI0707065A BRPI0707065B1 BR PI0707065 B1 BRPI0707065 B1 BR PI0707065B1 BR PI0707065 A BRPI0707065 A BR PI0707065A BR PI0707065 A BRPI0707065 A BR PI0707065A BR PI0707065 B1 BRPI0707065 B1 BR PI0707065B1
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- Prior art keywords
- polymer
- polymers
- zwitterionic
- gzn
- association
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- 229920000642 polymer Polymers 0.000 title claims abstract description 320
- 239000011343 solid material Substances 0.000 title claims abstract description 31
- 238000004381 surface treatment Methods 0.000 title claims abstract description 30
- 238000000034 method Methods 0.000 title claims abstract description 21
- 239000000203 mixture Substances 0.000 claims description 136
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- 239000000178 monomer Substances 0.000 claims description 76
- -1 alkylene radical Chemical class 0.000 claims description 58
- 229920003023 plastic Polymers 0.000 claims description 40
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- 125000002091 cationic group Chemical group 0.000 claims description 27
- 238000005406 washing Methods 0.000 claims description 25
- 125000000129 anionic group Chemical group 0.000 claims description 23
- 239000000463 material Substances 0.000 claims description 21
- 230000007935 neutral effect Effects 0.000 claims description 20
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- 125000000623 heterocyclic group Chemical group 0.000 claims description 2
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- 125000004178 (C1-C4) alkyl group Chemical group 0.000 description 1
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- FSSPGSAQUIYDCN-UHFFFAOYSA-N 1,3-Propane sultone Chemical compound O=S1(=O)CCCO1 FSSPGSAQUIYDCN-UHFFFAOYSA-N 0.000 description 1
- PQUXFUBNSYCQAL-UHFFFAOYSA-N 1-(2,3-difluorophenyl)ethanone Chemical compound CC(=O)C1=CC=CC(F)=C1F PQUXFUBNSYCQAL-UHFFFAOYSA-N 0.000 description 1
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- KBNPFIYSMUWBNA-UHFFFAOYSA-N 2-(dimethylamino)ethanesulfonic acid ethyl 2-methylprop-2-enoate Chemical compound CCOC(=O)C(C)=C.CN(C)CCS(O)(=O)=O KBNPFIYSMUWBNA-UHFFFAOYSA-N 0.000 description 1
- SZAXDKXHDBPOJW-UHFFFAOYSA-M 2-ethenyl-1-ethylpyridin-1-ium;bromide Chemical compound [Br-].CC[N+]1=CC=CC=C1C=C SZAXDKXHDBPOJW-UHFFFAOYSA-M 0.000 description 1
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- AGBXYHCHUYARJY-UHFFFAOYSA-N 2-phenylethenesulfonic acid Chemical compound OS(=O)(=O)C=CC1=CC=CC=C1 AGBXYHCHUYARJY-UHFFFAOYSA-N 0.000 description 1
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- 229920002472 Starch Polymers 0.000 description 1
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- 125000005250 alkyl acrylate group Chemical group 0.000 description 1
- 150000008052 alkyl sulfonates Chemical class 0.000 description 1
- 125000003277 amino group Chemical group 0.000 description 1
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- 150000001450 anions Chemical class 0.000 description 1
- 239000012736 aqueous medium Substances 0.000 description 1
- 125000000732 arylene group Chemical group 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- CADWTSSKOVRVJC-UHFFFAOYSA-N benzyl(dimethyl)azanium;chloride Chemical compound [Cl-].C[NH+](C)CC1=CC=CC=C1 CADWTSSKOVRVJC-UHFFFAOYSA-N 0.000 description 1
- 230000003115 biocidal effect Effects 0.000 description 1
- INLLPKCGLOXCIV-UHFFFAOYSA-N bromoethene Chemical compound BrC=C INLLPKCGLOXCIV-UHFFFAOYSA-N 0.000 description 1
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 1
- 150000001768 cations Chemical class 0.000 description 1
- 229920002678 cellulose Polymers 0.000 description 1
- 235000010980 cellulose Nutrition 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
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- 238000010276 construction Methods 0.000 description 1
- 238000013461 design Methods 0.000 description 1
- 150000001993 dienes Chemical class 0.000 description 1
- AEOFJEPZYYVYNV-UHFFFAOYSA-N dimethyl(3-sulfopropyl)azanium N-propylprop-2-enimidate Chemical compound CCCN=C([O-])C=C.C[NH+](C)CCCS(O)(=O)=O AEOFJEPZYYVYNV-UHFFFAOYSA-N 0.000 description 1
- SYJFEGQWDCRVNX-UHFFFAOYSA-N diquat Chemical compound C1=CC=[N+]2CC[N+]3=CC=CC=C3C2=C1 SYJFEGQWDCRVNX-UHFFFAOYSA-N 0.000 description 1
- 239000012153 distilled water Substances 0.000 description 1
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- 230000007717 exclusion Effects 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 239000004744 fabric Substances 0.000 description 1
- 239000001530 fumaric acid Substances 0.000 description 1
- 238000007306 functionalization reaction Methods 0.000 description 1
- 238000007429 general method Methods 0.000 description 1
- 239000003292 glue Substances 0.000 description 1
- 150000002334 glycols Chemical class 0.000 description 1
- 239000010439 graphite Substances 0.000 description 1
- 229910002804 graphite Inorganic materials 0.000 description 1
- PYGSKMBEVAICCR-UHFFFAOYSA-N hexa-1,5-diene Chemical group C=CCCC=C PYGSKMBEVAICCR-UHFFFAOYSA-N 0.000 description 1
- 125000001183 hydrocarbyl group Chemical group 0.000 description 1
- 230000003301 hydrolyzing effect Effects 0.000 description 1
- 125000002768 hydroxyalkyl group Chemical group 0.000 description 1
- MTNDZQHUAFNZQY-UHFFFAOYSA-N imidazoline Chemical compound C1CN=CN1 MTNDZQHUAFNZQY-UHFFFAOYSA-N 0.000 description 1
- 238000010348 incorporation Methods 0.000 description 1
- 230000000977 initiatory effect Effects 0.000 description 1
- 150000008040 ionic compounds Chemical class 0.000 description 1
- 125000003010 ionic group Chemical group 0.000 description 1
- 229920000831 ionic polymer Polymers 0.000 description 1
- 238000002955 isolation Methods 0.000 description 1
- 238000002372 labelling Methods 0.000 description 1
- VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 description 1
- 150000002689 maleic acids Chemical class 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- JDSHMPZPIAZGSV-UHFFFAOYSA-N melamine Chemical compound NC1=NC(N)=NC(N)=N1 JDSHMPZPIAZGSV-UHFFFAOYSA-N 0.000 description 1
- LVHBHZANLOWSRM-UHFFFAOYSA-N methylenebutanedioic acid Natural products OC(=O)CC(=C)C(O)=O LVHBHZANLOWSRM-UHFFFAOYSA-N 0.000 description 1
- 239000010413 mother solution Substances 0.000 description 1
- 229940088644 n,n-dimethylacrylamide Drugs 0.000 description 1
- YLGYACDQVQQZSW-UHFFFAOYSA-N n,n-dimethylprop-2-enamide Chemical compound CN(C)C(=O)C=C YLGYACDQVQQZSW-UHFFFAOYSA-N 0.000 description 1
- QYMUDOWMRHNHHP-UHFFFAOYSA-N n-[4-(dimethylamino)butyl]prop-2-enamide Chemical compound CN(C)CCCCNC(=O)C=C QYMUDOWMRHNHHP-UHFFFAOYSA-N 0.000 description 1
- ZQXSMRAEXCEDJD-UHFFFAOYSA-N n-ethenylformamide Chemical compound C=CNC=O ZQXSMRAEXCEDJD-UHFFFAOYSA-N 0.000 description 1
- QNILTEGFHQSKFF-UHFFFAOYSA-N n-propan-2-ylprop-2-enamide Chemical compound CC(C)NC(=O)C=C QNILTEGFHQSKFF-UHFFFAOYSA-N 0.000 description 1
- XFHJDMUEHUHAJW-UHFFFAOYSA-N n-tert-butylprop-2-enamide Chemical compound CC(C)(C)NC(=O)C=C XFHJDMUEHUHAJW-UHFFFAOYSA-N 0.000 description 1
- KKFHAJHLJHVUDM-UHFFFAOYSA-N n-vinylcarbazole Chemical compound C1=CC=C2N(C=C)C3=CC=CC=C3C2=C1 KKFHAJHLJHVUDM-UHFFFAOYSA-N 0.000 description 1
- 239000003921 oil Substances 0.000 description 1
- 238000005457 optimization Methods 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- MHYFEEDKONKGEB-UHFFFAOYSA-N oxathiane 2,2-dioxide Chemical compound O=S1(=O)CCCCO1 MHYFEEDKONKGEB-UHFFFAOYSA-N 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 125000004430 oxygen atom Chemical group O* 0.000 description 1
- 238000010422 painting Methods 0.000 description 1
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 description 1
- 239000010452 phosphate Substances 0.000 description 1
- ACVYVLVWPXVTIT-UHFFFAOYSA-M phosphinate Chemical compound [O-][PH2]=O ACVYVLVWPXVTIT-UHFFFAOYSA-M 0.000 description 1
- XYFCBTPGUUZFHI-UHFFFAOYSA-O phosphonium Chemical compound [PH4+] XYFCBTPGUUZFHI-UHFFFAOYSA-O 0.000 description 1
- 150000003013 phosphoric acid derivatives Chemical class 0.000 description 1
- 150000003014 phosphoric acid esters Chemical class 0.000 description 1
- 229910052698 phosphorus Inorganic materials 0.000 description 1
- 239000011574 phosphorus Substances 0.000 description 1
- 229920003229 poly(methyl methacrylate) Polymers 0.000 description 1
- 229920001281 polyalkylene Polymers 0.000 description 1
- 229920000447 polyanionic polymer Polymers 0.000 description 1
- 229920000728 polyester Polymers 0.000 description 1
- 229920000570 polyether Polymers 0.000 description 1
- 229920001223 polyethylene glycol Polymers 0.000 description 1
- 229920000193 polymethacrylate Polymers 0.000 description 1
- 239000004926 polymethyl methacrylate Substances 0.000 description 1
- 229920001451 polypropylene glycol Polymers 0.000 description 1
- 229920001282 polysaccharide Polymers 0.000 description 1
- 239000005017 polysaccharide Substances 0.000 description 1
- UIIIBRHUICCMAI-UHFFFAOYSA-N prop-2-ene-1-sulfonic acid Chemical compound OS(=O)(=O)CC=C UIIIBRHUICCMAI-UHFFFAOYSA-N 0.000 description 1
- SCUZVMOVTVSBLE-UHFFFAOYSA-N prop-2-enenitrile;styrene Chemical compound C=CC#N.C=CC1=CC=CC=C1 SCUZVMOVTVSBLE-UHFFFAOYSA-N 0.000 description 1
- JUJWROOIHBZHMG-UHFFFAOYSA-O pyridinium Chemical compound C1=CC=[NH+]C=C1 JUJWROOIHBZHMG-UHFFFAOYSA-O 0.000 description 1
- 125000001453 quaternary ammonium group Chemical group 0.000 description 1
- 238000005956 quaternization reaction Methods 0.000 description 1
- 238000010526 radical polymerization reaction Methods 0.000 description 1
- 238000005096 rolling process Methods 0.000 description 1
- 238000007789 sealing Methods 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 229940047670 sodium acrylate Drugs 0.000 description 1
- 238000001228 spectrum Methods 0.000 description 1
- 235000019698 starch Nutrition 0.000 description 1
- 229920000638 styrene acrylonitrile Polymers 0.000 description 1
- 239000011145 styrene acrylonitrile resin Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 150000003512 tertiary amines Chemical class 0.000 description 1
- 239000004416 thermosoftening plastic Substances 0.000 description 1
- FZGFBJMPSHGTRQ-UHFFFAOYSA-M trimethyl(2-prop-2-enoyloxyethyl)azanium;chloride Chemical compound [Cl-].C[N+](C)(C)CCOC(=O)C=C FZGFBJMPSHGTRQ-UHFFFAOYSA-M 0.000 description 1
- USFMMZYROHDWPJ-UHFFFAOYSA-N trimethyl-[2-(2-methylprop-2-enoyloxy)ethyl]azanium Chemical compound CC(=C)C(=O)OCC[N+](C)(C)C USFMMZYROHDWPJ-UHFFFAOYSA-N 0.000 description 1
- UZNHKBFIBYXPDV-UHFFFAOYSA-N trimethyl-[3-(2-methylprop-2-enoylamino)propyl]azanium;chloride Chemical compound [Cl-].CC(=C)C(=O)NCCC[N+](C)(C)C UZNHKBFIBYXPDV-UHFFFAOYSA-N 0.000 description 1
- ZTWTYVWXUKTLCP-UHFFFAOYSA-N vinylphosphonic acid Chemical compound OP(O)(=O)C=C ZTWTYVWXUKTLCP-UHFFFAOYSA-N 0.000 description 1
- 230000000007 visual effect Effects 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L101/00—Compositions of unspecified macromolecular compounds
- C08L101/02—Compositions of unspecified macromolecular compounds characterised by the presence of specified groups, e.g. terminal or pendant functional groups
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
- Graft Or Block Polymers (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Detergent Compositions (AREA)
- Treatments Of Macromolecular Shaped Articles (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| FR0601928 | 2006-03-03 | ||
| FR0601928A FR2898067B1 (fr) | 2006-03-03 | 2006-03-03 | Modification de surfaces solides par des associations de polymeres |
| PCT/FR2007/000385 WO2007099239A2 (fr) | 2006-03-03 | 2007-03-05 | Modification de surfaces solides par des associations de polymeres |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| BRPI0707065A2 BRPI0707065A2 (pt) | 2011-04-19 |
| BRPI0707065B1 true BRPI0707065B1 (pt) | 2019-02-05 |
Family
ID=37308883
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| BRPI0707065A BRPI0707065B1 (pt) | 2006-03-03 | 2007-03-05 | uso de uma associação de polímeros, método de tratamento de superfície de um material sólido, material sólido de superfície modificada e associações de polímeros |
Country Status (8)
| Country | Link |
|---|---|
| US (1) | US8883262B2 (https=) |
| EP (1) | EP1991620A2 (https=) |
| JP (1) | JP5611525B2 (https=) |
| CN (1) | CN101437901B (https=) |
| AU (1) | AU2007220381B2 (https=) |
| BR (1) | BRPI0707065B1 (https=) |
| FR (1) | FR2898067B1 (https=) |
| WO (1) | WO2007099239A2 (https=) |
Families Citing this family (41)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FR2894585B1 (fr) * | 2005-12-14 | 2012-04-27 | Rhodia Recherches Et Tech | Copolymere comprenant des unites zwitterioniques et d'autres unites, composition comprenant le copolymere, et utilisation |
| MX2009007101A (es) | 2006-12-29 | 2009-12-01 | Univ Washington | Superficies y materiales antibioincrustación bifuncionales. |
| US9533006B2 (en) | 2007-11-19 | 2017-01-03 | University Of Washington | Marine coatings |
| US8658192B2 (en) | 2007-11-19 | 2014-02-25 | University Of Washington | Integrated antimicrobial and low fouling materials |
| AU2008326438B2 (en) * | 2007-11-19 | 2014-09-04 | University Of Washington | Cationic betaine precursors to zwitterionic betaines having controlled biological properties |
| EP2352796A1 (en) | 2008-12-05 | 2011-08-10 | Semprus Biociences Corporation | Layered non-fouling, antimicrobial, antithrombogenic coatings |
| GB0911531D0 (en) * | 2009-07-02 | 2009-08-12 | Regent Medical Ltd | puncture indicating gloves |
| CN102906127A (zh) | 2009-11-06 | 2013-01-30 | 华盛顿大学商业中心 | 来自两性离子聚合物的自组装颗粒以及相关的方法 |
| JP5868862B2 (ja) | 2009-11-06 | 2016-02-24 | ユニヴァーシティ・オブ・ワシントン・スルー・イッツ・センター・フォー・コマーシャリゼーション | 双性イオンポリマーバイオコンジュゲートおよび関連する方法 |
| WO2011146394A1 (en) * | 2010-05-17 | 2011-11-24 | Millipore Corporation | Stimulus responsive polymers for the purification of biomolecules |
| JP5690671B2 (ja) * | 2010-06-30 | 2015-03-25 | 富士フイルム株式会社 | 新規な重合性組成物及びそれに用いる重合性化合物、並びに新規な重合性組成物を用いた画像形成材料及び平版印刷版原版 |
| CA2872378C (en) | 2011-07-20 | 2016-01-12 | University Of Washington Through Its Center For Commercialization | Photonic blood typing |
| WO2013090790A1 (en) | 2011-12-14 | 2013-06-20 | Semprus Biosciences Corp. | Silicone hydrogel contact lens modified using lanthanide or transition metal oxidants |
| CA2858730C (en) | 2011-12-14 | 2017-07-18 | Semprus Biosciences Corp. | Surface modified contact lenses |
| CA2859195C (en) | 2011-12-14 | 2016-09-27 | Semprus Biosciences Corp. | Imbibing process for contact lens surface modification |
| US9000063B2 (en) | 2011-12-14 | 2015-04-07 | Semprus Biosciences Corporation | Multistep UV process to create surface modified contact lenses |
| US9120119B2 (en) | 2011-12-14 | 2015-09-01 | Semprus Biosciences Corporation | Redox processes for contact lens modification |
| US10031138B2 (en) | 2012-01-20 | 2018-07-24 | University Of Washington Through Its Center For Commercialization | Hierarchical films having ultra low fouling and high recognition element loading properties |
| FR2989686B1 (fr) | 2012-04-18 | 2015-03-06 | Rhodia Operations | Traitement de formations souterraines par des gels |
| EP2812091B1 (en) | 2012-09-17 | 2021-03-10 | W.R. Grace & CO. - CONN. | Chromatography media and devices |
| EP2811983B1 (en) | 2012-09-17 | 2019-05-01 | W.R. Grace & CO. - CONN. | Functionalized particulate support material and methods of making and using the same |
| ES2887110T3 (es) | 2014-01-16 | 2021-12-21 | Grace W R & Co | Medios para cromatografía de afinidad y dispositivos para cromatografía |
| PL3137209T3 (pl) | 2014-05-02 | 2023-01-02 | W.R. Grace & Co. - Conn. | Funkcjonalizowany materiał nośnikowy i sposoby wytwarzania oraz stosowania funkcjonalizowanego materiału nośnikowego |
| US9782727B2 (en) | 2014-07-14 | 2017-10-10 | International Business Machines Corporation | Filtration membranes with functionalized star polymers |
| US10005042B2 (en) | 2015-02-16 | 2018-06-26 | International Business Machines Corporation | Thin film composite forward osmosis membranes with performance enhancing layers |
| US9931598B2 (en) | 2015-02-16 | 2018-04-03 | International Business Machines Corporation | Anti-fouling coatings with star polymers for filtration membranes |
| JP6482642B2 (ja) * | 2015-02-17 | 2019-03-13 | 富士フイルム株式会社 | 重合用組成物およびその製造方法、これを含むコーティング用組成物、これらを用いたコーティング用組成物の製造方法ならびにコーティングの製造方法 |
| KR102566292B1 (ko) | 2015-06-05 | 2023-08-10 | 더블유.알. 그레이스 앤드 캄파니-콘. | 흡착성 바이오프로세싱 정화제와 이의 제조 및 사용 방법 |
| EP3159384A1 (en) * | 2015-10-20 | 2017-04-26 | Rhodia Operations | Cationic polysaccharide-based primary coatings for hydrophobic surfaces |
| WO2018065210A1 (en) | 2016-10-03 | 2018-04-12 | Unilever N.V. | Water clarification composition containing amphoteric polymer |
| WO2018155578A1 (ja) * | 2017-02-27 | 2018-08-30 | リンテック株式会社 | 親水性組成物、及び親水性構造体 |
| MX2019015216A (es) | 2017-06-29 | 2020-02-05 | Unilever Nv | Composicion para la purificacion de agua turbia. |
| WO2019131757A1 (ja) * | 2017-12-27 | 2019-07-04 | 国立大学法人山形大学 | 両性イオンポリマー、その製造方法、及び両性イオンポリマーを含むタンパク質安定化剤 |
| WO2019185393A1 (en) | 2018-03-29 | 2019-10-03 | Unilever N.V. | Metal-free water clarification composition |
| EP3802629B1 (en) * | 2018-06-04 | 2024-05-01 | Specialty Operations France | Methods for reducing or preventing colloids adhesion and/or fouling on a substrate, compositions, and copolymers useful therefor |
| CN109731752B (zh) * | 2019-01-16 | 2020-11-03 | 吉林大学 | 一种在物品表面制备具有自清洁功能的高分子涂层的方法 |
| US20220251411A1 (en) * | 2019-07-09 | 2022-08-11 | Rhodia Operations | Methods for resisting frost on a substrate, compositions, and copolymers useful therefor |
| CN114829537B (zh) * | 2019-12-24 | 2024-05-28 | 东京应化工业株式会社 | 表面处理液及亲水化处理方法 |
| EP4136179A4 (en) * | 2020-04-15 | 2024-05-15 | Syensqo Sa | COATING COMPOSITION, USE AND METHOD FOR PRODUCING A FROST-PROOF SUBSTRATE |
| JP2023180172A (ja) * | 2022-06-08 | 2023-12-20 | 花王株式会社 | 表面処理組成物 |
| JP2023180173A (ja) * | 2022-06-08 | 2023-12-20 | 花王株式会社 | 表面処理組成物 |
Family Cites Families (14)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US6090901A (en) * | 1991-07-05 | 2000-07-18 | Biocompatibles Limited | Polymeric surface coatings |
| US6743878B2 (en) * | 1991-07-05 | 2004-06-01 | Biocompatibles Uk Limited | Polymeric surface coatings |
| GB9226791D0 (en) * | 1992-12-23 | 1993-02-17 | Biocompatibles Ltd | New materials |
| EP0875552A1 (en) * | 1997-04-30 | 1998-11-04 | The Procter & Gamble Company | Acidic limescale removal compositions |
| EP0875551A1 (en) * | 1997-04-30 | 1998-11-04 | The Procter & Gamble Company | Self-thickened acidic cleaning compositions |
| US6893595B1 (en) * | 1998-07-17 | 2005-05-17 | Biocompatibles Uk Limited | Method for providing coated moulded polymeric articles |
| FR2796390B1 (fr) * | 1999-07-15 | 2001-10-26 | Rhodia Chimie Sa | Utilisation d'un polymere amphotere pour traiter une surface dure |
| US6437040B2 (en) * | 1999-09-01 | 2002-08-20 | Rhodia Chimie | Water-soluble block copolymers comprising a hydrophilic block and a hydrophobic block |
| GB9924502D0 (en) * | 1999-10-15 | 1999-12-15 | Biocompatibles Ltd | Polymer blend materials |
| GB2398571A (en) * | 2003-02-22 | 2004-08-25 | Reckitt Benckiser Inc | Acidic hard surface cleaning and/or disinfecting composition |
| FR2833966B1 (fr) * | 2001-12-21 | 2007-02-09 | Rhodia Chimie Sa | Utilisation de polymeres statistiques amphiphiles charges pour epaissir des phases comprenant des micelles geantes de tensioactifs et composition aqueuse les comprenant |
| FR2839977B1 (fr) * | 2002-05-27 | 2005-08-12 | Rhodia Chimie Sa | Utilisation, dans une composition lavante et rincante de la vaisselle en machine, d'un copolymere amphotere comme agent anti-redeposition des salissures |
| FR2851572B1 (fr) * | 2003-02-20 | 2007-04-06 | Rhodia Chimie Sa | Composition nettoyante ou rincante pour surfaces dures |
| US20060183863A1 (en) * | 2005-02-14 | 2006-08-17 | Ciphergen Biosystems, Inc. | Zwitterionic polymers |
-
2006
- 2006-03-03 FR FR0601928A patent/FR2898067B1/fr not_active Expired - Lifetime
-
2007
- 2007-03-05 BR BRPI0707065A patent/BRPI0707065B1/pt active IP Right Grant
- 2007-03-05 CN CN200780016011.7A patent/CN101437901B/zh active Active
- 2007-03-05 JP JP2008557794A patent/JP5611525B2/ja not_active Expired - Fee Related
- 2007-03-05 EP EP07731084A patent/EP1991620A2/fr not_active Withdrawn
- 2007-03-05 WO PCT/FR2007/000385 patent/WO2007099239A2/fr not_active Ceased
- 2007-03-05 AU AU2007220381A patent/AU2007220381B2/en not_active Ceased
- 2007-03-05 US US12/281,597 patent/US8883262B2/en active Active
Also Published As
| Publication number | Publication date |
|---|---|
| US20090306292A1 (en) | 2009-12-10 |
| US8883262B2 (en) | 2014-11-11 |
| CN101437901A (zh) | 2009-05-20 |
| JP2009528440A (ja) | 2009-08-06 |
| AU2007220381A1 (en) | 2007-09-07 |
| WO2007099239A2 (fr) | 2007-09-07 |
| BRPI0707065A2 (pt) | 2011-04-19 |
| AU2007220381B2 (en) | 2012-05-17 |
| JP5611525B2 (ja) | 2014-10-22 |
| FR2898067B1 (fr) | 2008-05-30 |
| EP1991620A2 (fr) | 2008-11-19 |
| CN101437901B (zh) | 2014-07-30 |
| WO2007099239A3 (fr) | 2007-10-25 |
| FR2898067A1 (fr) | 2007-09-07 |
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