JP2008534714A5 - - Google Patents
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- JP2008534714A5 JP2008534714A5 JP2008503106A JP2008503106A JP2008534714A5 JP 2008534714 A5 JP2008534714 A5 JP 2008534714A5 JP 2008503106 A JP2008503106 A JP 2008503106A JP 2008503106 A JP2008503106 A JP 2008503106A JP 2008534714 A5 JP2008534714 A5 JP 2008534714A5
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- 229920000642 polymer Polymers 0.000 claims description 21
- 229920001519 homopolymer Polymers 0.000 claims description 19
- 125000000217 alkyl group Chemical group 0.000 claims description 12
- 125000004432 carbon atom Chemical group C* 0.000 claims description 12
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 claims description 10
- 239000000178 monomer Substances 0.000 claims description 10
- 150000003242 quaternary ammonium salts Chemical class 0.000 claims description 10
- 229910052710 silicon Inorganic materials 0.000 claims description 10
- 239000010703 silicon Substances 0.000 claims description 10
- 125000003118 aryl group Chemical group 0.000 claims description 7
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 7
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 claims description 6
- 125000000129 anionic group Chemical group 0.000 claims description 5
- 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 claims description 5
- WSFMFXQNYPNYGG-UHFFFAOYSA-M dimethyl-octadecyl-(3-trimethoxysilylpropyl)azanium;chloride Chemical group [Cl-].CCCCCCCCCCCCCCCCCC[N+](C)(C)CCC[Si](OC)(OC)OC WSFMFXQNYPNYGG-UHFFFAOYSA-M 0.000 claims description 4
- 229910052736 halogen Inorganic materials 0.000 claims description 4
- 150000002367 halogens Chemical class 0.000 claims description 4
- 125000000962 organic group Chemical group 0.000 claims description 4
- 150000003839 salts Chemical class 0.000 claims description 4
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 claims description 2
- 150000001875 compounds Chemical class 0.000 claims description 2
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 2
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 claims description 2
- 239000000126 substance Substances 0.000 claims description 2
- 238000000034 method Methods 0.000 claims 22
- 239000000758 substrate Substances 0.000 claims 15
- 229910052757 nitrogen Inorganic materials 0.000 claims 10
- 230000000845 anti-microbial effect Effects 0.000 claims 7
- 239000007787 solid Substances 0.000 claims 7
- 239000000243 solution Substances 0.000 claims 7
- 239000000203 mixture Substances 0.000 claims 6
- 239000002904 solvent Substances 0.000 claims 6
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims 5
- 230000002459 sustained effect Effects 0.000 claims 5
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 claims 4
- 125000003545 alkoxy group Chemical group 0.000 claims 4
- 238000002156 mixing Methods 0.000 claims 4
- VHUUQVKOLVNVRT-UHFFFAOYSA-N Ammonium hydroxide Chemical compound [NH4+].[OH-] VHUUQVKOLVNVRT-UHFFFAOYSA-N 0.000 claims 3
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 claims 3
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 claims 3
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 claims 3
- 125000005233 alkylalcohol group Chemical group 0.000 claims 3
- 239000000908 ammonium hydroxide Substances 0.000 claims 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims 3
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 claims 2
- YNAVUWVOSKDBBP-UHFFFAOYSA-N Morpholine Chemical compound C1COCCN1 YNAVUWVOSKDBBP-UHFFFAOYSA-N 0.000 claims 2
- 239000004721 Polyphenylene oxide Substances 0.000 claims 2
- 230000000844 anti-bacterial effect Effects 0.000 claims 2
- 125000004429 atom Chemical group 0.000 claims 2
- 125000002485 formyl group Chemical class [H]C(*)=O 0.000 claims 2
- -1 glycol ethers Chemical class 0.000 claims 2
- 229910052739 hydrogen Inorganic materials 0.000 claims 2
- 230000007062 hydrolysis Effects 0.000 claims 2
- 238000006460 hydrolysis reaction Methods 0.000 claims 2
- 238000004519 manufacturing process Methods 0.000 claims 2
- 239000000463 material Substances 0.000 claims 2
- 239000002245 particle Substances 0.000 claims 2
- 125000005010 perfluoroalkyl group Chemical group 0.000 claims 2
- 229920000570 polyether Polymers 0.000 claims 2
- 229920005989 resin Polymers 0.000 claims 2
- 239000011347 resin Substances 0.000 claims 2
- 229920006395 saturated elastomer Polymers 0.000 claims 2
- 229920005992 thermoplastic resin Polymers 0.000 claims 2
- JNYAEWCLZODPBN-JGWLITMVSA-N (2r,3r,4s)-2-[(1r)-1,2-dihydroxyethyl]oxolane-3,4-diol Chemical compound OC[C@@H](O)[C@H]1OC[C@H](O)[C@H]1O JNYAEWCLZODPBN-JGWLITMVSA-N 0.000 claims 1
- CPELXLSAUQHCOX-UHFFFAOYSA-M Bromide Chemical compound [Br-] CPELXLSAUQHCOX-UHFFFAOYSA-M 0.000 claims 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 claims 1
- IGFHQQFPSIBGKE-UHFFFAOYSA-N Nonylphenol Natural products CCCCCCCCCC1=CC=C(O)C=C1 IGFHQQFPSIBGKE-UHFFFAOYSA-N 0.000 claims 1
- 229910003849 O-Si Inorganic materials 0.000 claims 1
- 229910003872 O—Si Inorganic materials 0.000 claims 1
- 239000002202 Polyethylene glycol Substances 0.000 claims 1
- 125000002777 acetyl group Chemical group [H]C([H])([H])C(*)=O 0.000 claims 1
- 125000003668 acetyloxy group Chemical group [H]C([H])([H])C(=O)O[*] 0.000 claims 1
- 125000002252 acyl group Chemical group 0.000 claims 1
- 150000001298 alcohols Chemical class 0.000 claims 1
- 125000002723 alicyclic group Chemical group 0.000 claims 1
- 125000001931 aliphatic group Chemical group 0.000 claims 1
- 150000001338 aliphatic hydrocarbons Chemical class 0.000 claims 1
- 150000001408 amides Chemical class 0.000 claims 1
- 229920002118 antimicrobial polymer Polymers 0.000 claims 1
- 150000004982 aromatic amines Chemical class 0.000 claims 1
- 150000004945 aromatic hydrocarbons Chemical class 0.000 claims 1
- 230000015572 biosynthetic process Effects 0.000 claims 1
- 239000004566 building material Substances 0.000 claims 1
- 150000007942 carboxylates Chemical class 0.000 claims 1
- 239000003054 catalyst Substances 0.000 claims 1
- 239000011248 coating agent Substances 0.000 claims 1
- 238000000576 coating method Methods 0.000 claims 1
- 238000009833 condensation Methods 0.000 claims 1
- 230000005494 condensation Effects 0.000 claims 1
- 125000004122 cyclic group Chemical group 0.000 claims 1
- ZBCBWPMODOFKDW-UHFFFAOYSA-N diethanolamine Chemical compound OCCNCCO ZBCBWPMODOFKDW-UHFFFAOYSA-N 0.000 claims 1
- 238000007580 dry-mixing Methods 0.000 claims 1
- 238000001035 drying Methods 0.000 claims 1
- 150000002148 esters Chemical class 0.000 claims 1
- 238000001704 evaporation Methods 0.000 claims 1
- 125000000524 functional group Chemical group 0.000 claims 1
- 150000008282 halocarbons Chemical class 0.000 claims 1
- 125000000623 heterocyclic group Chemical group 0.000 claims 1
- 239000001257 hydrogen Substances 0.000 claims 1
- 125000004435 hydrogen atom Chemical class [H]* 0.000 claims 1
- XMBWDFGMSWQBCA-UHFFFAOYSA-N hydrogen iodide Chemical compound I XMBWDFGMSWQBCA-UHFFFAOYSA-N 0.000 claims 1
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 claims 1
- 238000002347 injection Methods 0.000 claims 1
- 239000007924 injection Substances 0.000 claims 1
- 150000002576 ketones Chemical class 0.000 claims 1
- 230000002045 lasting effect Effects 0.000 claims 1
- 230000005923 long-lasting effect Effects 0.000 claims 1
- 238000003801 milling Methods 0.000 claims 1
- 150000007522 mineralic acids Chemical class 0.000 claims 1
- SFDJOSRHYKHMOK-UHFFFAOYSA-N nitramide Chemical compound N[N+]([O-])=O SFDJOSRHYKHMOK-UHFFFAOYSA-N 0.000 claims 1
- SNQQPOLDUKLAAF-UHFFFAOYSA-N nonylphenol Chemical compound CCCCCCCCCC1=CC=CC=C1O SNQQPOLDUKLAAF-UHFFFAOYSA-N 0.000 claims 1
- 150000007524 organic acids Chemical class 0.000 claims 1
- 235000005985 organic acids Nutrition 0.000 claims 1
- 229910052760 oxygen Inorganic materials 0.000 claims 1
- 229920001223 polyethylene glycol Polymers 0.000 claims 1
- 229920001451 polypropylene glycol Polymers 0.000 claims 1
- 239000000843 powder Substances 0.000 claims 1
- 238000001556 precipitation Methods 0.000 claims 1
- 239000002243 precursor Substances 0.000 claims 1
- 125000001453 quaternary ammonium group Chemical group 0.000 claims 1
- 238000005507 spraying Methods 0.000 claims 1
- 125000000547 substituted alkyl group Chemical group 0.000 claims 1
- 229910052717 sulfur Inorganic materials 0.000 claims 1
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 claims 1
- 229920002554 vinyl polymer Polymers 0.000 claims 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 4
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 3
- SNRUBQQJIBEYMU-UHFFFAOYSA-N Dodecane Chemical group CCCCCCCCCCCC SNRUBQQJIBEYMU-UHFFFAOYSA-N 0.000 description 2
- 125000003438 dodecyl group Chemical group [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])* 0.000 description 2
- 125000001421 myristyl 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])[H] 0.000 description 2
- 125000002347 octyl 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])[H] 0.000 description 2
- 150000003841 chloride salts Chemical group 0.000 description 1
- 150000004820 halides Chemical class 0.000 description 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US66422205P | 2005-03-22 | 2005-03-22 | |
| US70220105P | 2005-07-25 | 2005-07-25 | |
| PCT/US2006/010318 WO2006102367A1 (en) | 2005-03-22 | 2006-03-22 | Method of creating a solvent-free polymeric silicon-containing quaternary ammonium antimicrobial agent having superior sustained antimicrobial properties |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JP2008534714A JP2008534714A (ja) | 2008-08-28 |
| JP2008534714A5 true JP2008534714A5 (enExample) | 2009-05-07 |
Family
ID=37969989
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2008503106A Pending JP2008534714A (ja) | 2005-03-22 | 2006-03-22 | 優れた持続性の抗菌特性を有する、無溶媒のシリコン含有第４級アンモニウムを含むポリマー抗菌剤の作製法 |
Country Status (6)
| Country | Link |
|---|---|
| US (2) | US7858141B2 (enExample) |
| EP (1) | EP1863865B1 (enExample) |
| JP (1) | JP2008534714A (enExample) |
| CA (1) | CA2601594A1 (enExample) |
| MX (1) | MX2007011771A (enExample) |
| WO (2) | WO2006102366A1 (enExample) |
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| JP4358190B2 (ja) * | 2005-03-16 | 2009-11-04 | 日東電工株式会社 | 粘着剤組成物、粘着シート類および表面保護フィルム |
| JP4067017B2 (ja) * | 2005-04-26 | 2008-03-26 | セイコーエプソン株式会社 | マイクロレンズ基板の製造方法、マイクロレンズ基板、液晶パネル用対向基板、液晶パネルおよび投射型表示装置 |
| WO2006123638A1 (ja) * | 2005-05-20 | 2006-11-23 | Nitto Denko Corporation | 粘着剤組成物、粘着シートおよび表面保護フィルム |
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| US9839213B2 (en) | 2011-10-14 | 2017-12-12 | The University Of Georgia Research Foundation, Inc. | Photochemical cross-linkable polymers, methods of making photochemical cross-linkable polymers, methods of using photochemical cross-linkable polymers, and methods of making articles containing photochemical cross-linkable polymers |
| WO2013079957A1 (en) * | 2011-11-30 | 2013-06-06 | Coventry University | Antimicrobial animal product |
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| CN105517585B (zh) | 2013-04-26 | 2019-11-22 | 生物相互作用有限公司 | 生物活性涂层 |
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| EP3244734A4 (en) | 2015-01-13 | 2018-07-18 | Biosyn Inc. | Solid antimicrobial compositions with enhanced solubility |
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| CN106188419B (zh) * | 2016-07-25 | 2018-08-21 | 东南大学 | 接枝聚合物及基于表面接枝的抗菌软镜的制备方法 |
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| KR102375857B1 (ko) * | 2017-11-27 | 2022-03-16 | 주식회사 엘지화학 | 고흡수성 수지 조성물 |
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| WO2021234162A2 (fr) | 2020-05-22 | 2021-11-25 | Lithcote-Europe | Revêtement nano-céramique, hybride, transparent et biocide pour support solide et support solide comportant un tel revêtement et son procédé d'obtention |
| IT202000030179A1 (it) | 2020-12-11 | 2022-06-11 | Crossing Srl | Trattamenti antimicrobici superficiali |
| US12195183B2 (en) | 2020-12-18 | 2025-01-14 | Goodrich Corporation | Antimicrobial coating surface treatment systems and methods for aircraft faucets |
| BE1029530B1 (fr) | 2021-06-25 | 2023-01-30 | Sichem | Procédé d'obtention d'un revêtement |
| BE1029958B1 (fr) | 2021-11-24 | 2023-06-19 | Sichem | Revêtement biocide amélioré |
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-
2006
- 2006-03-22 EP EP20060739201 patent/EP1863865B1/en active Active
- 2006-03-22 WO PCT/US2006/010317 patent/WO2006102366A1/en not_active Ceased
- 2006-03-22 CA CA 2601594 patent/CA2601594A1/en not_active Abandoned
- 2006-03-22 US US11/386,348 patent/US7858141B2/en active Active
- 2006-03-22 MX MX2007011771A patent/MX2007011771A/es active IP Right Grant
- 2006-03-22 JP JP2008503106A patent/JP2008534714A/ja active Pending
- 2006-03-22 WO PCT/US2006/010318 patent/WO2006102367A1/en not_active Ceased
- 2006-03-22 US US11/386,485 patent/US7851653B2/en active Active
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