ES2257489T3 - Agentes de inhibicion de pelicula. - Google Patents
Agentes de inhibicion de pelicula.Info
- Publication number
- ES2257489T3 ES2257489T3 ES02014040T ES02014040T ES2257489T3 ES 2257489 T3 ES2257489 T3 ES 2257489T3 ES 02014040 T ES02014040 T ES 02014040T ES 02014040 T ES02014040 T ES 02014040T ES 2257489 T3 ES2257489 T3 ES 2257489T3
- Authority
- ES
- Spain
- Prior art keywords
- film
- moiety
- carbon atoms
- hydrogen
- enamel
- 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
- 230000005764 inhibitory process Effects 0.000 title claims description 5
- 239000000203 mixture Substances 0.000 claims abstract description 72
- 125000000217 alkyl group Chemical group 0.000 claims abstract description 15
- 150000002894 organic compounds Chemical class 0.000 claims abstract description 15
- 125000003545 alkoxy group Chemical group 0.000 claims abstract description 7
- -1 ester compound Chemical class 0.000 claims abstract description 7
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims abstract description 7
- 125000000753 cycloalkyl group Chemical group 0.000 claims abstract description 6
- 125000003710 aryl alkyl group Chemical group 0.000 claims abstract description 3
- 210000003298 dental enamel Anatomy 0.000 claims description 70
- 125000004432 carbon atom Chemical group C* 0.000 claims description 23
- 239000003795 chemical substances by application Substances 0.000 claims description 20
- 238000001035 drying Methods 0.000 claims description 19
- 229910052739 hydrogen Inorganic materials 0.000 claims description 18
- 239000001257 hydrogen Substances 0.000 claims description 18
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 13
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 10
- 230000003647 oxidation Effects 0.000 claims description 10
- 238000007254 oxidation reaction Methods 0.000 claims description 10
- 230000002401 inhibitory effect Effects 0.000 claims description 9
- 150000002431 hydrogen Chemical class 0.000 claims description 8
- 239000003973 paint Substances 0.000 claims description 7
- 239000000976 ink Substances 0.000 claims description 4
- 239000003960 organic solvent Substances 0.000 claims description 4
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims description 3
- 125000004429 atom Chemical group 0.000 claims description 3
- 229910052799 carbon Inorganic materials 0.000 claims description 3
- 239000006185 dispersion Substances 0.000 claims description 3
- 239000000839 emulsion Substances 0.000 claims description 3
- 125000003118 aryl group Chemical group 0.000 claims description 2
- TUJKJAMUKRIRHC-UHFFFAOYSA-N hydroxyl Chemical compound [OH] TUJKJAMUKRIRHC-UHFFFAOYSA-N 0.000 claims description 2
- 239000007921 spray Substances 0.000 claims description 2
- 125000003277 amino group Chemical group 0.000 claims 4
- 238000004040 coloring Methods 0.000 claims 1
- 150000001875 compounds Chemical class 0.000 abstract description 6
- 150000002443 hydroxylamines Chemical class 0.000 abstract description 4
- 150000001732 carboxylic acid derivatives Chemical class 0.000 abstract description 2
- 150000001299 aldehydes Chemical class 0.000 abstract 1
- 150000002690 malonic acid derivatives Chemical class 0.000 abstract 1
- 230000015572 biosynthetic process Effects 0.000 description 31
- 239000000654 additive Substances 0.000 description 25
- 239000002274 desiccant Substances 0.000 description 25
- WHIVNJATOVLWBW-UHFFFAOYSA-N n-butan-2-ylidenehydroxylamine Chemical compound CCC(C)=NO WHIVNJATOVLWBW-UHFFFAOYSA-N 0.000 description 25
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 24
- 239000003112 inhibitor Substances 0.000 description 23
- 238000009472 formulation Methods 0.000 description 22
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 18
- 230000000996 additive effect Effects 0.000 description 18
- 229910052791 calcium Inorganic materials 0.000 description 18
- 239000011575 calcium Substances 0.000 description 18
- 229920001174 Diethylhydroxylamine Polymers 0.000 description 17
- FVCOIAYSJZGECG-UHFFFAOYSA-N diethylhydroxylamine Chemical compound CCN(O)CC FVCOIAYSJZGECG-UHFFFAOYSA-N 0.000 description 17
- 229910017052 cobalt Inorganic materials 0.000 description 14
- 239000010941 cobalt Substances 0.000 description 14
- GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt atom Chemical compound [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 description 14
- 235000019589 hardness Nutrition 0.000 description 12
- 239000011230 binding agent Substances 0.000 description 11
- 229920000180 alkyd Polymers 0.000 description 10
- 239000011521 glass Substances 0.000 description 9
- 239000007787 solid Substances 0.000 description 7
- 150000001412 amines Chemical group 0.000 description 5
- 229910052760 oxygen Inorganic materials 0.000 description 5
- 239000001301 oxygen Substances 0.000 description 5
- 239000002904 solvent Substances 0.000 description 5
- 239000000126 substance Substances 0.000 description 5
- 238000004383 yellowing Methods 0.000 description 5
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 4
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 4
- OFOBLEOULBTSOW-UHFFFAOYSA-N Malonic acid Chemical compound OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 4
- SUAKHGWARZSWIH-UHFFFAOYSA-N N,N‐diethylformamide Chemical compound CCN(CC)C=O SUAKHGWARZSWIH-UHFFFAOYSA-N 0.000 description 4
- QCWXUUIWCKQGHC-UHFFFAOYSA-N Zirconium Chemical compound [Zr] QCWXUUIWCKQGHC-UHFFFAOYSA-N 0.000 description 4
- YRKCREAYFQTBPV-UHFFFAOYSA-N acetylacetone Chemical compound CC(=O)CC(C)=O YRKCREAYFQTBPV-UHFFFAOYSA-N 0.000 description 4
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 4
- 230000001934 delay Effects 0.000 description 4
- 229910052751 metal Inorganic materials 0.000 description 4
- 239000002184 metal Substances 0.000 description 4
- GXELTROTKVKZBQ-UHFFFAOYSA-N n,n-dibenzylhydroxylamine Chemical compound C=1C=CC=CC=1CN(O)CC1=CC=CC=C1 GXELTROTKVKZBQ-UHFFFAOYSA-N 0.000 description 4
- 229920005989 resin Polymers 0.000 description 4
- 239000011347 resin Substances 0.000 description 4
- 229910052726 zirconium Inorganic materials 0.000 description 4
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 3
- AVXURJPOCDRRFD-UHFFFAOYSA-N Hydroxylamine Chemical group ON AVXURJPOCDRRFD-UHFFFAOYSA-N 0.000 description 3
- ATWLCPHWYPSRBQ-UHFFFAOYSA-N N-Methylacetoacetamide Chemical compound CNC(=O)CC(C)=O ATWLCPHWYPSRBQ-UHFFFAOYSA-N 0.000 description 3
- 241001085205 Prenanthella exigua Species 0.000 description 3
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 3
- 239000002253 acid Substances 0.000 description 3
- 229910052788 barium Inorganic materials 0.000 description 3
- DSAJWYNOEDNPEQ-UHFFFAOYSA-N barium atom Chemical compound [Ba] DSAJWYNOEDNPEQ-UHFFFAOYSA-N 0.000 description 3
- RAXXELZNTBOGNW-UHFFFAOYSA-N imidazole Natural products C1=CNC=N1 RAXXELZNTBOGNW-UHFFFAOYSA-N 0.000 description 3
- 239000003921 oil Substances 0.000 description 3
- 150000002923 oximes Chemical class 0.000 description 3
- 239000000243 solution Substances 0.000 description 3
- 229910052725 zinc Inorganic materials 0.000 description 3
- 239000011701 zinc Substances 0.000 description 3
- OAKJQQAXSVQMHS-UHFFFAOYSA-N Hydrazine Chemical group NN OAKJQQAXSVQMHS-UHFFFAOYSA-N 0.000 description 2
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 2
- 150000007513 acids Chemical class 0.000 description 2
- 150000001298 alcohols Chemical class 0.000 description 2
- 239000007864 aqueous solution Substances 0.000 description 2
- 150000002148 esters Chemical class 0.000 description 2
- VYSYZMNJHYOXGN-UHFFFAOYSA-N ethyl n-aminocarbamate Chemical compound CCOC(=O)NN VYSYZMNJHYOXGN-UHFFFAOYSA-N 0.000 description 2
- BDAGIHXWWSANSR-UHFFFAOYSA-N methanoic acid Natural products OC=O BDAGIHXWWSANSR-UHFFFAOYSA-N 0.000 description 2
- 239000011877 solvent mixture Substances 0.000 description 2
- OSWFIVFLDKOXQC-UHFFFAOYSA-N 4-(3-methoxyphenyl)aniline Chemical compound COC1=CC=CC(C=2C=CC(N)=CC=2)=C1 OSWFIVFLDKOXQC-UHFFFAOYSA-N 0.000 description 1
- VHUUQVKOLVNVRT-UHFFFAOYSA-N Ammonium hydroxide Chemical group [NH4+].[OH-] VHUUQVKOLVNVRT-UHFFFAOYSA-N 0.000 description 1
- 241000272201 Columbiformes Species 0.000 description 1
- 239000004593 Epoxy Substances 0.000 description 1
- 206010019695 Hepatic neoplasm Diseases 0.000 description 1
- 241000699670 Mus sp. Species 0.000 description 1
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 1
- XBDQKXXYIPTUBI-UHFFFAOYSA-M Propionate Chemical compound CCC([O-])=O XBDQKXXYIPTUBI-UHFFFAOYSA-M 0.000 description 1
- 241000700159 Rattus Species 0.000 description 1
- 125000001931 aliphatic group Chemical group 0.000 description 1
- 239000000908 ammonium hydroxide Chemical group 0.000 description 1
- 150000004982 aromatic amines Chemical class 0.000 description 1
- 150000001491 aromatic compounds Chemical class 0.000 description 1
- 239000012928 buffer substance Substances 0.000 description 1
- 150000007942 carboxylates Chemical class 0.000 description 1
- 231100000357 carcinogen Toxicity 0.000 description 1
- 239000003183 carcinogenic agent Substances 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 238000004140 cleaning Methods 0.000 description 1
- 239000011248 coating agent Substances 0.000 description 1
- 238000000576 coating method Methods 0.000 description 1
- 230000000536 complexating effect Effects 0.000 description 1
- 150000001991 dicarboxylic acids Chemical class 0.000 description 1
- BEPAFCGSDWSTEL-UHFFFAOYSA-N dimethyl malonate Chemical compound COC(=O)CC(=O)OC BEPAFCGSDWSTEL-UHFFFAOYSA-N 0.000 description 1
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 description 1
- 230000007613 environmental effect Effects 0.000 description 1
- 150000002170 ethers Chemical class 0.000 description 1
- 235000019253 formic acid Nutrition 0.000 description 1
- WBJINCZRORDGAQ-UHFFFAOYSA-N formic acid ethyl ester Natural products CCOC=O WBJINCZRORDGAQ-UHFFFAOYSA-N 0.000 description 1
- 238000010348 incorporation Methods 0.000 description 1
- 231100000037 inhalation toxicity test Toxicity 0.000 description 1
- 150000002576 ketones Chemical class 0.000 description 1
- 208000014018 liver neoplasm Diseases 0.000 description 1
- 230000007774 longterm Effects 0.000 description 1
- 238000000034 method Methods 0.000 description 1
- 230000001590 oxidative effect Effects 0.000 description 1
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N phenol group Chemical group C1(=CC=CC=C1)O ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 1
- 150000002989 phenols Chemical class 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 230000002265 prevention Effects 0.000 description 1
- 150000003217 pyrazoles Chemical class 0.000 description 1
- 238000010186 staining Methods 0.000 description 1
- 231100000419 toxicity Toxicity 0.000 description 1
- 230000001988 toxicity Effects 0.000 description 1
- 230000002110 toxicologic effect Effects 0.000 description 1
- 231100000723 toxicological property Toxicity 0.000 description 1
- 229910052723 transition metal Inorganic materials 0.000 description 1
- 150000003624 transition metals Chemical class 0.000 description 1
- 238000009827 uniform distribution Methods 0.000 description 1
- 239000008096 xylene Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
- C09D11/00—Inks
- C09D11/02—Printing inks
- C09D11/03—Printing inks characterised by features other than the chemical nature of the binder
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
- C09D7/00—Features of coating compositions, not provided for in group C09D5/00; Processes for incorporating ingredients in coating compositions
- C09D7/40—Additives
- C09D7/46—Anti-skinning agents
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K5/00—Use of organic ingredients
- C08K5/04—Oxygen-containing compounds
- C08K5/07—Aldehydes; Ketones
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K5/00—Use of organic ingredients
- C08K5/16—Nitrogen-containing compounds
- C08K5/17—Amines; Quaternary ammonium compounds
Landscapes
- Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Wood Science & Technology (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Paints Or Removers (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Thermotherapy And Cooling Therapy Devices (AREA)
- Massaging Devices (AREA)
- Finger-Pressure Massage (AREA)
- Prostheses (AREA)
- Materials For Medical Uses (AREA)
- Inks, Pencil-Leads, Or Crayons (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE10133727 | 2001-07-11 | ||
| DE10133727A DE10133727A1 (de) | 2001-07-11 | 2001-07-11 | Verwendung von Mischungen spezieller organischer Verbindungen als Hautverhinderungsmittel in lufttrocknenden Lacken |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| ES2257489T3 true ES2257489T3 (es) | 2006-08-01 |
Family
ID=7691415
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ES02014040T Expired - Lifetime ES2257489T3 (es) | 2001-07-11 | 2002-06-28 | Agentes de inhibicion de pelicula. |
Country Status (11)
| Country | Link |
|---|---|
| US (3) | US6730157B2 (enExample) |
| EP (1) | EP1275701B1 (enExample) |
| JP (1) | JP2003055584A (enExample) |
| AT (1) | ATE318869T1 (enExample) |
| CA (1) | CA2392786C (enExample) |
| DE (2) | DE10133727A1 (enExample) |
| DK (1) | DK1275701T3 (enExample) |
| ES (1) | ES2257489T3 (enExample) |
| MX (1) | MXPA02006807A (enExample) |
| NO (1) | NO327262B1 (enExample) |
| PT (1) | PT1275701E (enExample) |
Families Citing this family (17)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE50305112D1 (de) * | 2003-04-01 | 2006-11-02 | Tetenal Ag & Co Kg | Ink-Jet Tinte |
| KR101166359B1 (ko) | 2004-06-02 | 2012-07-27 | 아르끄마 프랑스 | 피막방지 화합물 및 이를 함유하는 조성물 |
| EP1778777B1 (en) * | 2004-06-02 | 2010-11-10 | Arkema France | Antiskinning compound and compositions containing them |
| US7253222B2 (en) * | 2004-06-02 | 2007-08-07 | Arkema Inc. | Antiskinning compound and compositions containing them |
| KR100717007B1 (ko) | 2005-07-02 | 2007-05-10 | 삼성전자주식회사 | 잉크 조성물, 이를 포함한 잉크 카트리지 및 잉크 젯트기록 장치 |
| US7201796B2 (en) * | 2005-07-27 | 2007-04-10 | Arkema Inc. | Antiskinning compound and compositions containing them |
| US20070049657A1 (en) * | 2005-08-23 | 2007-03-01 | Martyak Nicholas M | Antiskinning compound and compositions containing them |
| US7316977B2 (en) * | 2005-08-24 | 2008-01-08 | Air Products And Chemicals, Inc. | Chemical-mechanical planarization composition having ketooxime compounds and associated method for use |
| US20070044689A1 (en) * | 2005-08-30 | 2007-03-01 | Martyak Nicholas M | Antiskinning compound and compositions containing them |
| US20080250977A1 (en) * | 2007-04-16 | 2008-10-16 | Andrew Mason | Oxime free anti-skinning combination |
| EP2474578A1 (en) * | 2011-01-06 | 2012-07-11 | Rahu Catalytics Limited | Antiskinning compositions |
| DK3077467T3 (da) | 2013-12-03 | 2023-01-09 | Ppg Europe B V | Sikkativsammensætning og anvendelse deraf |
| EP3204459B1 (en) * | 2014-10-09 | 2018-08-15 | PPG Europe B.V. | Coating composition comprising anti-skinning agent |
| EP3296372B1 (de) | 2016-09-19 | 2020-03-04 | Daw Se | Lösemittelhaltige beschichtungsmasse |
| PL3296353T3 (pl) | 2016-09-19 | 2022-05-30 | Daw Se | Masa powłokowa zawierająca rozpuszczalnik do powłok malarskich |
| EP3434738B1 (de) | 2017-07-28 | 2020-09-02 | Daw Se | Lösemittelhaltige farbtonpaste |
| CN112646415A (zh) * | 2019-11-26 | 2021-04-13 | 安徽亚伟标识工程有限公司 | 一种改进标识牌绿色印刷油墨的环保添加剂与制备方法 |
Family Cites Families (18)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE1519103A1 (de) * | 1964-12-18 | 1969-12-11 | Dehydag Gmbh | N,N-dialkylierte Hydroxylamine als Hautverhuetungsmittel |
| US4009175A (en) * | 1976-03-15 | 1977-02-22 | The Upjohn Company | 1-[(Aminooxy)-methyl]-6-substituted-4H-s-triazolo[4,3-a][1,4] benzodiazepines |
| CA1143080A (en) * | 1979-11-19 | 1983-03-15 | Bertram Zuckert | Process for producing improved aqueous emulsions of air drying and stoving alkyd resins |
| JPS5815553A (ja) | 1981-07-21 | 1983-01-28 | Tokai Denka Kogyo Kk | フエニル樹脂の脱色及び着色防止法 |
| DE3418988A1 (de) * | 1984-05-22 | 1985-11-28 | Basf Ag, 6700 Ludwigshafen | (alpha)-hydroxyketone als hautverhinderungsmittel |
| JPS624478A (ja) | 1985-06-28 | 1987-01-10 | Kansai Paint Co Ltd | 内面塗装缶の製造方法 |
| DE3635285A1 (de) * | 1986-10-16 | 1988-04-21 | Henkel Kgaa | Lufttrocknendes lackbindemittel auf basis von polyoctenylen |
| US4720566A (en) * | 1986-10-23 | 1988-01-19 | Betz Laboratories, Inc. | Method and composition for inhibiting acrylonitrile polymerization |
| AT388921B (de) * | 1987-06-17 | 1989-09-25 | Vianova Kunstharz Ag | Wasserverduennbare streichlacke auf der basis von wasserloeslichen alkydharzen |
| US5981454A (en) * | 1993-06-21 | 1999-11-09 | Ekc Technology, Inc. | Post clean treatment composition comprising an organic acid and hydroxylamine |
| CN1073137C (zh) * | 1995-11-28 | 2001-10-17 | 大日本油墨化学工业株式会社 | 水基涂料用固化性树脂组合物 |
| JPH107935A (ja) | 1996-06-20 | 1998-01-13 | Daiyuu Paint Kk | セメント系セラミックス塗料 |
| JPH1017629A (ja) | 1996-07-04 | 1998-01-20 | Kayaku Akzo Kk | ハードコート用樹脂組成物及びその硬化方法 |
| US6262169B1 (en) * | 1998-05-14 | 2001-07-17 | Eastman Chemical Company | Protonated amines for controlled crosslinking of latex polymers |
| DE19741644A1 (de) * | 1997-09-22 | 1999-03-25 | Borchers Gmbh | Neue Additive zur Vermeidung von Hautbildung an lufttrocknenden Lacken |
| EP1115800A1 (en) * | 1998-08-24 | 2001-07-18 | Akzo Nobel N.V. | Anti-skinning agent for coating compositions |
| TWI225483B (en) * | 1998-10-16 | 2004-12-21 | Ciba Sc Holding Ag | Heterocyclic alkoxyamines as regulators in controlled radical polymerization process |
| EP1103583A1 (en) * | 1999-11-23 | 2001-05-30 | Condea Servo B.V. | Anti-skinning agents |
-
2001
- 2001-07-11 DE DE10133727A patent/DE10133727A1/de not_active Withdrawn
-
2002
- 2002-06-28 PT PT02014040T patent/PT1275701E/pt unknown
- 2002-06-28 DK DK02014040T patent/DK1275701T3/da active
- 2002-06-28 AT AT02014040T patent/ATE318869T1/de active
- 2002-06-28 EP EP02014040A patent/EP1275701B1/de not_active Expired - Lifetime
- 2002-06-28 ES ES02014040T patent/ES2257489T3/es not_active Expired - Lifetime
- 2002-06-28 DE DE50205906T patent/DE50205906D1/de not_active Expired - Lifetime
- 2002-07-01 JP JP2002192186A patent/JP2003055584A/ja active Pending
- 2002-07-08 US US10/191,382 patent/US6730157B2/en not_active Expired - Lifetime
- 2002-07-09 CA CA2392786A patent/CA2392786C/en not_active Expired - Lifetime
- 2002-07-10 NO NO20023325A patent/NO327262B1/no not_active IP Right Cessation
- 2002-07-10 MX MXPA02006807A patent/MXPA02006807A/es active IP Right Grant
-
2004
- 2004-03-26 US US10/811,349 patent/US20040177787A1/en not_active Abandoned
-
2006
- 2006-10-12 US US11/546,607 patent/US7344588B2/en not_active Expired - Lifetime
Also Published As
| Publication number | Publication date |
|---|---|
| CA2392786C (en) | 2010-08-17 |
| US7344588B2 (en) | 2008-03-18 |
| US20040177787A1 (en) | 2004-09-16 |
| NO20023325L (no) | 2003-01-13 |
| PT1275701E (pt) | 2006-05-31 |
| CA2392786A1 (en) | 2003-01-11 |
| EP1275701A1 (de) | 2003-01-15 |
| DE10133727A1 (de) | 2003-01-23 |
| MXPA02006807A (es) | 2004-12-13 |
| NO327262B1 (no) | 2009-05-25 |
| DE50205906D1 (de) | 2006-04-27 |
| US6730157B2 (en) | 2004-05-04 |
| JP2003055584A (ja) | 2003-02-26 |
| ATE318869T1 (de) | 2006-03-15 |
| NO20023325D0 (no) | 2002-07-10 |
| US20070022906A1 (en) | 2007-02-01 |
| US20030025105A1 (en) | 2003-02-06 |
| EP1275701B1 (de) | 2006-03-01 |
| DK1275701T3 (da) | 2006-06-26 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
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