KR20040015299A - 표면 처리 조성물 및 방법 - Google Patents
표면 처리 조성물 및 방법 Download PDFInfo
- Publication number
- KR20040015299A KR20040015299A KR10-2003-7016979A KR20037016979A KR20040015299A KR 20040015299 A KR20040015299 A KR 20040015299A KR 20037016979 A KR20037016979 A KR 20037016979A KR 20040015299 A KR20040015299 A KR 20040015299A
- Authority
- KR
- South Korea
- Prior art keywords
- formula
- compound
- composition
- group
- substrate
- 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.)
- Withdrawn
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- 239000000203 mixture Substances 0.000 title claims abstract description 61
- 238000000034 method Methods 0.000 title claims description 17
- 238000004381 surface treatment Methods 0.000 title claims description 14
- 239000000758 substrate Substances 0.000 claims abstract description 55
- 150000001875 compounds Chemical class 0.000 claims abstract description 40
- 239000007795 chemical reaction product Substances 0.000 claims abstract description 5
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 25
- 239000002904 solvent Substances 0.000 claims description 23
- 239000011521 glass Substances 0.000 claims description 12
- 125000004432 carbon atom Chemical group C* 0.000 claims description 11
- 238000006243 chemical reaction Methods 0.000 claims description 11
- 150000001298 alcohols Chemical class 0.000 claims description 10
- 239000003795 chemical substances by application Substances 0.000 claims description 10
- -1 oxypropylene groups Chemical group 0.000 claims description 10
- 239000004094 surface-active agent Substances 0.000 claims description 7
- 239000013543 active substance Substances 0.000 claims description 6
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 6
- 125000000217 alkyl group Chemical group 0.000 claims description 5
- 239000003054 catalyst Substances 0.000 claims description 5
- 150000002148 esters Chemical group 0.000 claims description 5
- 230000003301 hydrolyzing effect Effects 0.000 claims description 5
- 238000004519 manufacturing process Methods 0.000 claims description 5
- KXDHJXZQYSOELW-UHFFFAOYSA-M Carbamate Chemical group NC([O-])=O KXDHJXZQYSOELW-UHFFFAOYSA-M 0.000 claims description 4
- 239000004593 Epoxy Substances 0.000 claims description 4
- 125000003158 alcohol group Chemical group 0.000 claims description 4
- 239000000839 emulsion Substances 0.000 claims description 4
- 125000001033 ether group Chemical group 0.000 claims description 4
- 239000012948 isocyanate Substances 0.000 claims description 4
- 150000002513 isocyanates Chemical class 0.000 claims description 4
- 125000005702 oxyalkylene group Chemical group 0.000 claims description 3
- 229920003169 water-soluble polymer Polymers 0.000 claims description 3
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims description 2
- 125000003545 alkoxy group Chemical group 0.000 claims description 2
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 2
- 229910052799 carbon Inorganic materials 0.000 claims description 2
- 230000001804 emulsifying effect Effects 0.000 claims description 2
- 229910052736 halogen Inorganic materials 0.000 claims description 2
- 150000002367 halogens Chemical class 0.000 claims description 2
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 2
- 125000004433 nitrogen atom Chemical group N* 0.000 claims description 2
- 125000006353 oxyethylene group Chemical group 0.000 claims description 2
- 229910052760 oxygen Inorganic materials 0.000 claims description 2
- 239000001301 oxygen Substances 0.000 claims description 2
- 229920003229 poly(methyl methacrylate) Polymers 0.000 claims description 2
- 239000004417 polycarbonate Substances 0.000 claims description 2
- 229920000515 polycarbonate Polymers 0.000 claims description 2
- 239000004926 polymethyl methacrylate Substances 0.000 claims description 2
- 229910052717 sulfur Inorganic materials 0.000 claims description 2
- 239000011593 sulfur Substances 0.000 claims description 2
- 150000001735 carboxylic acids Chemical class 0.000 claims 1
- 238000011282 treatment Methods 0.000 abstract description 10
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Natural products CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 26
- 239000000243 solution Substances 0.000 description 24
- 238000004140 cleaning Methods 0.000 description 11
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 10
- 230000007062 hydrolysis Effects 0.000 description 9
- 238000006460 hydrolysis reaction Methods 0.000 description 9
- 239000003921 oil Substances 0.000 description 9
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 8
- 239000007788 liquid Substances 0.000 description 8
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 6
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 6
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 6
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 6
- 230000000052 comparative effect Effects 0.000 description 6
- 230000015572 biosynthetic process Effects 0.000 description 5
- 239000000428 dust Substances 0.000 description 5
- 239000000523 sample Substances 0.000 description 5
- 229910000077 silane Inorganic materials 0.000 description 5
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 4
- BLRPTPMANUNPDV-UHFFFAOYSA-N Silane Chemical compound [SiH4] BLRPTPMANUNPDV-UHFFFAOYSA-N 0.000 description 4
- 239000000356 contaminant Substances 0.000 description 4
- 238000011065 in-situ storage Methods 0.000 description 4
- 229910052757 nitrogen Inorganic materials 0.000 description 4
- 239000000047 product Substances 0.000 description 4
- 239000012429 reaction media Substances 0.000 description 4
- 238000010992 reflux Methods 0.000 description 4
- 238000003786 synthesis reaction Methods 0.000 description 4
- KZTQCLVQCSXKHV-UHFFFAOYSA-N 3-isocyanatopropylsilane Chemical compound [SiH3]CCCN=C=O KZTQCLVQCSXKHV-UHFFFAOYSA-N 0.000 description 3
- 238000005033 Fourier transform infrared spectroscopy Methods 0.000 description 3
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- 239000005662 Paraffin oil Substances 0.000 description 3
- 229910008051 Si-OH Inorganic materials 0.000 description 3
- 229910006358 Si—OH Inorganic materials 0.000 description 3
- ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 description 3
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
- 238000010438 heat treatment Methods 0.000 description 3
- 230000002209 hydrophobic effect Effects 0.000 description 3
- 239000000463 material Substances 0.000 description 3
- 238000002360 preparation method Methods 0.000 description 3
- DKPFZGUDAPQIHT-UHFFFAOYSA-N Butyl acetate Natural products CCCCOC(C)=O DKPFZGUDAPQIHT-UHFFFAOYSA-N 0.000 description 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 2
- NTIZESTWPVYFNL-UHFFFAOYSA-N Methyl isobutyl ketone Chemical compound CC(C)CC(C)=O NTIZESTWPVYFNL-UHFFFAOYSA-N 0.000 description 2
- UIHCLUNTQKBZGK-UHFFFAOYSA-N Methyl isobutyl ketone Natural products CCC(C)C(C)=O UIHCLUNTQKBZGK-UHFFFAOYSA-N 0.000 description 2
- 239000008186 active pharmaceutical agent Substances 0.000 description 2
- 230000003373 anti-fouling effect Effects 0.000 description 2
- 238000010533 azeotropic distillation Methods 0.000 description 2
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 2
- KRVSOGSZCMJSLX-UHFFFAOYSA-L chromic acid Substances O[Cr](O)(=O)=O KRVSOGSZCMJSLX-UHFFFAOYSA-L 0.000 description 2
- 238000011109 contamination Methods 0.000 description 2
- 238000004132 cross linking Methods 0.000 description 2
- SNRUBQQJIBEYMU-UHFFFAOYSA-N dodecane Chemical compound CCCCCCCCCCCC SNRUBQQJIBEYMU-UHFFFAOYSA-N 0.000 description 2
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 2
- 238000001704 evaporation Methods 0.000 description 2
- 230000008020 evaporation Effects 0.000 description 2
- AWJWCTOOIBYHON-UHFFFAOYSA-N furo[3,4-b]pyrazine-5,7-dione Chemical compound C1=CN=C2C(=O)OC(=O)C2=N1 AWJWCTOOIBYHON-UHFFFAOYSA-N 0.000 description 2
- JMMWKPVZQRWMSS-UHFFFAOYSA-N isopropanol acetate Natural products CC(C)OC(C)=O JMMWKPVZQRWMSS-UHFFFAOYSA-N 0.000 description 2
- 229940011051 isopropyl acetate Drugs 0.000 description 2
- GWYFCOCPABKNJV-UHFFFAOYSA-N isovaleric acid Chemical compound CC(C)CC(O)=O GWYFCOCPABKNJV-UHFFFAOYSA-N 0.000 description 2
- 150000002576 ketones Chemical class 0.000 description 2
- 230000014759 maintenance of location Effects 0.000 description 2
- 150000007522 mineralic acids Chemical class 0.000 description 2
- 150000007524 organic acids Chemical class 0.000 description 2
- 125000005010 perfluoroalkyl group Chemical group 0.000 description 2
- 150000003333 secondary alcohols Chemical class 0.000 description 2
- 238000005507 spraying Methods 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- BGHCVCJVXZWKCC-UHFFFAOYSA-N tetradecane Chemical compound CCCCCCCCCCCCCC BGHCVCJVXZWKCC-UHFFFAOYSA-N 0.000 description 2
- RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 description 1
- OZAIFHULBGXAKX-UHFFFAOYSA-N 2-(2-cyanopropan-2-yldiazenyl)-2-methylpropanenitrile Chemical compound N#CC(C)(C)N=NC(C)(C)C#N OZAIFHULBGXAKX-UHFFFAOYSA-N 0.000 description 1
- HNUQMTZUNUBOLQ-UHFFFAOYSA-N 2-[2-[2-[2-[2-[2-[2-[2-[2-(2-octadecoxyethoxy)ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethanol Chemical compound CCCCCCCCCCCCCCCCCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCO HNUQMTZUNUBOLQ-UHFFFAOYSA-N 0.000 description 1
- IMDPTYFNMLYSLH-UHFFFAOYSA-N 3-silylpropyl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OCCC[SiH3] IMDPTYFNMLYSLH-UHFFFAOYSA-N 0.000 description 1
- XDLMVUHYZWKMMD-UHFFFAOYSA-N 3-trimethoxysilylpropyl 2-methylprop-2-enoate Chemical compound CO[Si](OC)(OC)CCCOC(=O)C(C)=C XDLMVUHYZWKMMD-UHFFFAOYSA-N 0.000 description 1
- OZAIFHULBGXAKX-VAWYXSNFSA-N AIBN Substances N#CC(C)(C)\N=N\C(C)(C)C#N OZAIFHULBGXAKX-VAWYXSNFSA-N 0.000 description 1
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 1
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 1
- 241000209035 Ilex Species 0.000 description 1
- 229910002808 Si–O–Si Inorganic materials 0.000 description 1
- BOTDANWDWHJENH-UHFFFAOYSA-N Tetraethyl orthosilicate Chemical compound CCO[Si](OCC)(OCC)OCC BOTDANWDWHJENH-UHFFFAOYSA-N 0.000 description 1
- 238000005299 abrasion Methods 0.000 description 1
- 238000009825 accumulation Methods 0.000 description 1
- 230000003213 activating effect Effects 0.000 description 1
- 239000011149 active material Substances 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 239000012298 atmosphere Substances 0.000 description 1
- 239000011449 brick Substances 0.000 description 1
- 230000001680 brushing effect Effects 0.000 description 1
- 239000006227 byproduct Substances 0.000 description 1
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 description 1
- 150000001732 carboxylic acid derivatives Chemical class 0.000 description 1
- 238000006555 catalytic reaction Methods 0.000 description 1
- 239000000460 chlorine Substances 0.000 description 1
- 229910052801 chlorine Inorganic materials 0.000 description 1
- 230000003749 cleanliness Effects 0.000 description 1
- 239000011248 coating agent Substances 0.000 description 1
- 239000008199 coating composition Substances 0.000 description 1
- 238000000576 coating method Methods 0.000 description 1
- 239000004567 concrete Substances 0.000 description 1
- 238000010276 construction Methods 0.000 description 1
- 238000000151 deposition Methods 0.000 description 1
- 238000007865 diluting Methods 0.000 description 1
- 238000004090 dissolution Methods 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 230000007613 environmental effect Effects 0.000 description 1
- 125000004185 ester group Chemical group 0.000 description 1
- 150000002170 ethers Chemical class 0.000 description 1
- 125000001301 ethoxy group Chemical group [H]C([H])([H])C([H])([H])O* 0.000 description 1
- 239000004744 fabric Substances 0.000 description 1
- 230000005484 gravity Effects 0.000 description 1
- 239000004519 grease Substances 0.000 description 1
- 238000007654 immersion Methods 0.000 description 1
- 238000005470 impregnation Methods 0.000 description 1
- 239000012535 impurity Substances 0.000 description 1
- 239000003999 initiator Substances 0.000 description 1
- 238000002347 injection Methods 0.000 description 1
- 239000007924 injection Substances 0.000 description 1
- 239000010985 leather Substances 0.000 description 1
- 231100000053 low toxicity Toxicity 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 230000003287 optical effect Effects 0.000 description 1
- DOAMZWOPDPPKJS-UHFFFAOYSA-N oxiran-2-ol Chemical compound OC1CO1 DOAMZWOPDPPKJS-UHFFFAOYSA-N 0.000 description 1
- 150000002924 oxiranes Chemical class 0.000 description 1
- 239000012188 paraffin wax Substances 0.000 description 1
- 239000006072 paste Substances 0.000 description 1
- 229920000151 polyglycol Polymers 0.000 description 1
- 239000010695 polyglycol Substances 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 238000001556 precipitation Methods 0.000 description 1
- 239000002243 precursor Substances 0.000 description 1
- 125000000075 primary alcohol group Chemical group 0.000 description 1
- 238000010791 quenching Methods 0.000 description 1
- 230000000171 quenching effect Effects 0.000 description 1
- 230000005855 radiation Effects 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 150000004756 silanes Chemical class 0.000 description 1
- 239000004575 stone Substances 0.000 description 1
- 125000000101 thioether group Chemical group 0.000 description 1
- 150000003573 thiols Chemical class 0.000 description 1
- 239000012780 transparent material Substances 0.000 description 1
- FRGPKMWIYVTFIQ-UHFFFAOYSA-N triethoxy(3-isocyanatopropyl)silane Chemical compound CCO[Si](OCC)(OCC)CCCN=C=O FRGPKMWIYVTFIQ-UHFFFAOYSA-N 0.000 description 1
- 239000002023 wood Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F7/00—Compounds containing elements of Groups 4 or 14 of the Periodic Table
- C07F7/02—Silicon compounds
- C07F7/08—Compounds having one or more C—Si linkages
- C07F7/18—Compounds having one or more C—Si linkages as well as one or more C—O—Si linkages
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F7/00—Compounds containing elements of Groups 4 or 14 of the Periodic Table
- C07F7/02—Silicon compounds
- C07F7/08—Compounds having one or more C—Si linkages
- C07F7/12—Organo silicon halides
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F7/00—Compounds containing elements of Groups 4 or 14 of the Periodic Table
- C07F7/02—Silicon compounds
- C07F7/08—Compounds having one or more C—Si linkages
- C07F7/18—Compounds having one or more C—Si linkages as well as one or more C—O—Si linkages
- C07F7/1804—Compounds having Si-O-C linkages
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Polyethers (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Materials Applied To Surfaces To Minimize Adherence Of Mist Or Water (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| FR0108460A FR2826654B1 (fr) | 2001-06-27 | 2001-06-27 | Composition et procede de traitement de surface et substrats susceptibles d'etre ainsi obtenus |
| FR0108460 | 2001-06-27 | ||
| PCT/FR2002/002167 WO2003002572A1 (fr) | 2001-06-27 | 2002-06-21 | Composition et procede de traitement de surface |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| KR20040015299A true KR20040015299A (ko) | 2004-02-18 |
Family
ID=8864821
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| KR10-2003-7016979A Withdrawn KR20040015299A (ko) | 2001-06-27 | 2002-06-21 | 표면 처리 조성물 및 방법 |
Country Status (8)
| Country | Link |
|---|---|
| US (1) | US7276618B2 (enExample) |
| EP (1) | EP1436302B1 (enExample) |
| JP (1) | JP4527974B2 (enExample) |
| KR (1) | KR20040015299A (enExample) |
| CN (1) | CN1260232C (enExample) |
| DE (1) | DE60210645T2 (enExample) |
| FR (1) | FR2826654B1 (enExample) |
| WO (1) | WO2003002572A1 (enExample) |
Families Citing this family (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE102005056620A1 (de) * | 2005-11-25 | 2007-06-06 | Merck Patent Gmbh | Amphiphile Silane |
| CN101541816B (zh) * | 2006-12-15 | 2014-03-12 | 3M创新有限公司 | 用于表面处理的具有甲硅烷侧基的含氟氨基甲酸酯化合物 |
| EP2215029A4 (en) * | 2007-11-16 | 2017-11-15 | Aqua Diagnostic Pty Ltd | Photo electrodes |
| US8450513B2 (en) * | 2010-07-30 | 2013-05-28 | E I Du Pont De Nemours And Company | Silane compositions for polyester nanocomposites |
| US8691915B2 (en) | 2012-04-23 | 2014-04-08 | Sabic Innovative Plastics Ip B.V. | Copolymers and polymer blends having improved refractive indices |
| WO2016101185A1 (en) * | 2014-12-24 | 2016-06-30 | E. I. Du Pont De Nemours And Company | Perfluoropolyether silanes and method of forming the same |
Family Cites Families (30)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3012006A (en) | 1958-04-24 | 1961-12-05 | Dow Corning | Fluorinated alkyl silanes and their use |
| DE1232959B (de) | 1964-09-12 | 1967-01-26 | Walter Bloechl | Verfahren zur Herstellung eines aus waessriger Loesung anwendbaren Impraegniermittels |
| US3422131A (en) | 1966-02-10 | 1969-01-14 | Us Agriculture | Fluoroalkoxyalkyl silanes |
| US3442664A (en) | 1966-04-26 | 1969-05-06 | Minnesota Mining & Mfg | Treating composition,method of treating and treated surfaces |
| JPS5318008B2 (enExample) * | 1973-12-28 | 1978-06-13 | ||
| US4089882A (en) | 1974-03-22 | 1978-05-16 | Shin-Etsu Chemical Co., Ltd. | Method of preparing fluoroalkyl-containing organosilanes |
| JPS521926B2 (enExample) | 1974-03-25 | 1977-01-19 | ||
| US4525425A (en) | 1981-05-11 | 1985-06-25 | El-Chem Corporation | Water and oil repellent metal oxide-organic combination coating systems and method of making same |
| JPS60190727A (ja) * | 1984-03-09 | 1985-09-28 | Daikin Ind Ltd | 含フツ素有機シラン化合物およびその製法と用途 |
| EP0166363B1 (en) | 1984-06-26 | 1991-08-07 | Asahi Glass Company Ltd. | Low reflectance transparent material having antisoiling properties |
| US4549003A (en) | 1984-10-26 | 1985-10-22 | Dow Corning Corporation | Method for preparing novel fluorinated organosiloxane copolymers |
| US4689181A (en) | 1985-12-27 | 1987-08-25 | Dow Corning Corporation | Fluorine-containing organosilanes useful as magnetic media lubricants |
| US4648904A (en) | 1986-02-14 | 1987-03-10 | Scm Corporation | Aqueous systems containing silanes for rendering masonry surfaces water repellant |
| US5011963A (en) | 1988-02-09 | 1991-04-30 | Matsushita Electric Ind., Co., Ltd. | Terminal perfluoroalkylsilane compounds |
| US4990377A (en) | 1988-05-02 | 1991-02-05 | Pcr Group, Inc. | Buffered silane emulsions having low volatile organic compounds when cured |
| US4877654A (en) | 1988-05-02 | 1989-10-31 | Pcr, Inc. | Buffered silane emulsions for rendering porous substrates water repellent |
| JPH02252787A (ja) * | 1989-03-28 | 1990-10-11 | Daikin Ind Ltd | 防汚性撥水撥油剤組成物 |
| US5059649A (en) | 1989-11-08 | 1991-10-22 | Dow Corning Corporation | Storage stable one-part fluorosilicone gel compositions exhibiting improved thermal stability |
| US4983459A (en) | 1990-04-03 | 1991-01-08 | Ppg Industries, Inc. | Chemically reacted glass surface |
| US5051129A (en) | 1990-06-25 | 1991-09-24 | Dow Corning Corporation | Masonry water repellent composition |
| US5124467A (en) | 1990-07-20 | 1992-06-23 | Ciba-Geigy Corporation | Perfluoroalkypolyoxyalkylpolysiloxane surfactants |
| US5274159A (en) | 1993-02-18 | 1993-12-28 | Minnesota Mining And Manufacturing Company | Destructable fluorinated alkoxysilane surfactants and repellent coatings derived therefrom |
| JP3383849B2 (ja) * | 1993-07-03 | 2003-03-10 | 株式会社ソフト９９コーポレーション | めがねレンズの防曇剤 |
| JPH09241622A (ja) * | 1996-03-06 | 1997-09-16 | Shin Etsu Chem Co Ltd | 防汚加工剤組成物 |
| JP3503365B2 (ja) * | 1996-10-25 | 2004-03-02 | 旭硝子株式会社 | 表面処理された基材 |
| JP3849232B2 (ja) * | 1997-06-12 | 2006-11-22 | 東レ株式会社 | 光学薄膜、反射防止性物品および反射防止方法 |
| US5962188A (en) * | 1997-06-24 | 1999-10-05 | Kodak Polychrome Graphics Llc | Direct write lithographic printing plates |
| JP4477229B2 (ja) * | 1998-03-04 | 2010-06-09 | イー・アイ・デュポン・ドウ・ヌムール・アンド・カンパニー | 耐層剥離性積層ガラス構造体 |
| JP2000328230A (ja) * | 1999-05-20 | 2000-11-28 | Toray Ind Inc | 有機膜の成膜法 |
| JP2000327997A (ja) | 1999-05-20 | 2000-11-28 | Toray Ind Inc | 有機膜の成膜方法 |
-
2001
- 2001-06-27 FR FR0108460A patent/FR2826654B1/fr not_active Expired - Fee Related
-
2002
- 2002-06-21 JP JP2003508953A patent/JP4527974B2/ja not_active Expired - Fee Related
- 2002-06-21 US US10/477,986 patent/US7276618B2/en not_active Expired - Fee Related
- 2002-06-21 KR KR10-2003-7016979A patent/KR20040015299A/ko not_active Withdrawn
- 2002-06-21 EP EP02755082A patent/EP1436302B1/fr not_active Expired - Lifetime
- 2002-06-21 CN CNB028126548A patent/CN1260232C/zh not_active Expired - Fee Related
- 2002-06-21 DE DE60210645T patent/DE60210645T2/de not_active Expired - Lifetime
- 2002-06-21 WO PCT/FR2002/002167 patent/WO2003002572A1/fr not_active Ceased
Also Published As
| Publication number | Publication date |
|---|---|
| JP4527974B2 (ja) | 2010-08-18 |
| US7276618B2 (en) | 2007-10-02 |
| CN1520419A (zh) | 2004-08-11 |
| DE60210645T2 (de) | 2007-01-25 |
| JP2004530776A (ja) | 2004-10-07 |
| EP1436302A1 (fr) | 2004-07-14 |
| US20040176600A1 (en) | 2004-09-09 |
| HK1069829A1 (en) | 2005-06-03 |
| EP1436302B1 (fr) | 2006-04-12 |
| DE60210645D1 (de) | 2006-05-24 |
| WO2003002572A1 (fr) | 2003-01-09 |
| FR2826654B1 (fr) | 2005-09-16 |
| FR2826654A1 (fr) | 2003-01-03 |
| CN1260232C (zh) | 2006-06-21 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| PA0105 | International application |
Patent event date: 20031226 Patent event code: PA01051R01D Comment text: International Patent Application |
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| PG1501 | Laying open of application | ||
| PC1203 | Withdrawal of no request for examination | ||
| WITN | Application deemed withdrawn, e.g. because no request for examination was filed or no examination fee was paid |