ES262036A1 - Procedimiento para la preparar una composiciën formadora de pelicula de secado al aire - Google Patents
Procedimiento para la preparar una composiciën formadora de pelicula de secado al aireInfo
- Publication number
- ES262036A1 ES262036A1 ES0262036A ES262036A ES262036A1 ES 262036 A1 ES262036 A1 ES 262036A1 ES 0262036 A ES0262036 A ES 0262036A ES 262036 A ES262036 A ES 262036A ES 262036 A1 ES262036 A1 ES 262036A1
- Authority
- ES
- Spain
- Prior art keywords
- vinyl
- isopropenyl
- furyl
- beta
- group
- 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
Links
- 239000000203 mixture Substances 0.000 title abstract 9
- 238000007605 air drying Methods 0.000 title abstract 3
- 229920002554 vinyl polymer Polymers 0.000 abstract 20
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 abstract 17
- -1 tetrahydrophenyl Chemical group 0.000 abstract 13
- 125000000555 isopropenyl group Chemical group [H]\C([H])=C(\*)C([H])([H])[H] 0.000 abstract 12
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 abstract 8
- 239000000049 pigment Substances 0.000 abstract 8
- 229920005989 resin Polymers 0.000 abstract 8
- 239000011347 resin Substances 0.000 abstract 8
- 125000002941 2-furyl group Chemical group O1C([*])=C([H])C([H])=C1[H] 0.000 abstract 7
- 229910017052 cobalt Inorganic materials 0.000 abstract 6
- 239000010941 cobalt Substances 0.000 abstract 6
- GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt atom Chemical compound [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 abstract 6
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 abstract 6
- 125000004368 propenyl group Chemical group C(=CC)* 0.000 abstract 6
- 229910052751 metal Inorganic materials 0.000 abstract 5
- 239000002184 metal Substances 0.000 abstract 5
- KAKZBPTYRLMSJV-UHFFFAOYSA-N Butadiene Chemical compound C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 abstract 4
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 abstract 4
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 abstract 4
- 239000003054 catalyst Substances 0.000 abstract 4
- 150000001875 compounds Chemical class 0.000 abstract 4
- 150000002148 esters Chemical class 0.000 abstract 4
- 229910052742 iron Inorganic materials 0.000 abstract 4
- VCHQGHCBFOFZJK-UHFFFAOYSA-N 1-cyclopenta-1,3-dien-1-ylcyclopenta-1,3-diene Chemical group C1C=CC=C1C1=CC=CC1 VCHQGHCBFOFZJK-UHFFFAOYSA-N 0.000 abstract 3
- 125000006003 dichloroethyl group Chemical group 0.000 abstract 3
- 125000005043 dihydropyranyl group Chemical group O1C(CCC=C1)* 0.000 abstract 3
- 150000004862 dioxolanes Chemical class 0.000 abstract 3
- 239000001257 hydrogen Substances 0.000 abstract 3
- 229910052739 hydrogen Inorganic materials 0.000 abstract 3
- 125000004435 hydrogen atom Chemical group [H]* 0.000 abstract 3
- 125000001400 nonyl 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])[H] 0.000 abstract 3
- 229920006395 saturated elastomer Polymers 0.000 abstract 3
- WNXJIVFYUVYPPR-UHFFFAOYSA-N 1,3-dioxolane Chemical compound C1COCO1 WNXJIVFYUVYPPR-UHFFFAOYSA-N 0.000 abstract 2
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 abstract 2
- OEPOKWHJYJXUGD-UHFFFAOYSA-N 2-(3-phenylmethoxyphenyl)-1,3-thiazole-4-carbaldehyde Chemical compound O=CC1=CSC(C=2C=C(OCC=3C=CC=CC=3)C=CC=2)=N1 OEPOKWHJYJXUGD-UHFFFAOYSA-N 0.000 abstract 2
- MMEDJBFVJUFIDD-UHFFFAOYSA-N 2-[2-(carboxymethyl)phenyl]acetic acid Chemical compound OC(=O)CC1=CC=CC=C1CC(O)=O MMEDJBFVJUFIDD-UHFFFAOYSA-N 0.000 abstract 2
- OYHQOLUKZRVURQ-HZJYTTRNSA-M 9-cis,12-cis-Octadecadienoate Chemical compound CCCCC\C=C/C\C=C/CCCCCCCC([O-])=O OYHQOLUKZRVURQ-HZJYTTRNSA-M 0.000 abstract 2
- HGINCPLSRVDWNT-UHFFFAOYSA-N Acrolein Chemical compound C=CC=O HGINCPLSRVDWNT-UHFFFAOYSA-N 0.000 abstract 2
- RGCKGOZRHPZPFP-UHFFFAOYSA-N Alizarin Natural products C1=CC=C2C(=O)C3=C(O)C(O)=CC=C3C(=O)C2=C1 RGCKGOZRHPZPFP-UHFFFAOYSA-N 0.000 abstract 2
- 235000009328 Amaranthus caudatus Nutrition 0.000 abstract 2
- 240000001592 Amaranthus caudatus Species 0.000 abstract 2
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 abstract 2
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 abstract 2
- 229920000459 Nitrile rubber Polymers 0.000 abstract 2
- 239000000020 Nitrocellulose Substances 0.000 abstract 2
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 abstract 2
- BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 abstract 2
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 abstract 2
- FJWGYAHXMCUOOM-QHOUIDNNSA-N [(2s,3r,4s,5r,6r)-2-[(2r,3r,4s,5r,6s)-4,5-dinitrooxy-2-(nitrooxymethyl)-6-[(2r,3r,4s,5r,6s)-4,5,6-trinitrooxy-2-(nitrooxymethyl)oxan-3-yl]oxyoxan-3-yl]oxy-3,5-dinitrooxy-6-(nitrooxymethyl)oxan-4-yl] nitrate Chemical compound O([C@@H]1O[C@@H]([C@H]([C@H](O[N+]([O-])=O)[C@H]1O[N+]([O-])=O)O[C@H]1[C@@H]([C@@H](O[N+]([O-])=O)[C@H](O[N+]([O-])=O)[C@@H](CO[N+]([O-])=O)O1)O[N+]([O-])=O)CO[N+](=O)[O-])[C@@H]1[C@@H](CO[N+]([O-])=O)O[C@@H](O[N+]([O-])=O)[C@H](O[N+]([O-])=O)[C@H]1O[N+]([O-])=O FJWGYAHXMCUOOM-QHOUIDNNSA-N 0.000 abstract 2
- HFVAFDPGUJEFBQ-UHFFFAOYSA-M alizarin red S Chemical compound [Na+].O=C1C2=CC=CC=C2C(=O)C2=C1C=C(S([O-])(=O)=O)C(O)=C2O HFVAFDPGUJEFBQ-UHFFFAOYSA-M 0.000 abstract 2
- 229920000180 alkyd Polymers 0.000 abstract 2
- 235000012735 amaranth Nutrition 0.000 abstract 2
- 239000004178 amaranth Substances 0.000 abstract 2
- 229920005549 butyl rubber Polymers 0.000 abstract 2
- 229920002301 cellulose acetate Polymers 0.000 abstract 2
- 229920006217 cellulose acetate butyrate Polymers 0.000 abstract 2
- WOTPFVNWMLFMFW-UHFFFAOYSA-N chembl1967257 Chemical compound OC1=CC=C2C=CC=CC2=C1N=NC1=CC=C([N+]([O-])=O)C=C1 WOTPFVNWMLFMFW-UHFFFAOYSA-N 0.000 abstract 2
- 239000003795 chemical substances by application Substances 0.000 abstract 2
- ZCDOYSPFYFSLEW-UHFFFAOYSA-N chromate(2-) Chemical class [O-][Cr]([O-])(=O)=O ZCDOYSPFYFSLEW-UHFFFAOYSA-N 0.000 abstract 2
- 150000001868 cobalt Chemical class 0.000 abstract 2
- 239000003086 colorant Substances 0.000 abstract 2
- 229920001577 copolymer Polymers 0.000 abstract 2
- 229910052802 copper Inorganic materials 0.000 abstract 2
- 239000010949 copper Substances 0.000 abstract 2
- 150000001991 dicarboxylic acids Chemical class 0.000 abstract 2
- 229920001971 elastomer Polymers 0.000 abstract 2
- 239000000806 elastomer Substances 0.000 abstract 2
- 125000002573 ethenylidene group Chemical group [*]=C=C([H])[H] 0.000 abstract 2
- 239000011133 lead Substances 0.000 abstract 2
- 229940049918 linoleate Drugs 0.000 abstract 2
- WPBNNNQJVZRUHP-UHFFFAOYSA-L manganese(2+);methyl n-[[2-(methoxycarbonylcarbamothioylamino)phenyl]carbamothioyl]carbamate;n-[2-(sulfidocarbothioylamino)ethyl]carbamodithioate Chemical compound [Mn+2].[S-]C(=S)NCCNC([S-])=S.COC(=O)NC(=S)NC1=CC=CC=C1NC(=S)NC(=O)OC WPBNNNQJVZRUHP-UHFFFAOYSA-L 0.000 abstract 2
- 229910044991 metal oxide Inorganic materials 0.000 abstract 2
- 150000004706 metal oxides Chemical class 0.000 abstract 2
- 229910052914 metal silicate Inorganic materials 0.000 abstract 2
- 229910052976 metal sulfide Inorganic materials 0.000 abstract 2
- 150000002739 metals Chemical class 0.000 abstract 2
- GEMHFKXPOCTAIP-UHFFFAOYSA-N n,n-dimethyl-n'-phenylcarbamimidoyl chloride Chemical compound CN(C)C(Cl)=NC1=CC=CC=C1 GEMHFKXPOCTAIP-UHFFFAOYSA-N 0.000 abstract 2
- 229910052759 nickel Inorganic materials 0.000 abstract 2
- 229920001220 nitrocellulos Polymers 0.000 abstract 2
- ZQPPMHVWECSIRJ-KTKRTIGZSA-M oleate Chemical compound CCCCCCCC\C=C/CCCCCCCC([O-])=O ZQPPMHVWECSIRJ-KTKRTIGZSA-M 0.000 abstract 2
- 229940049964 oleate Drugs 0.000 abstract 2
- 150000002894 organic compounds Chemical class 0.000 abstract 2
- IEQIEDJGQAUEQZ-UHFFFAOYSA-N phthalocyanine Chemical compound N1C(N=C2C3=CC=CC=C3C(N=C3C4=CC=CC=C4C(=N4)N3)=N2)=C(C=CC=C2)C2=C1N=C1C2=CC=CC=C2C4=N1 IEQIEDJGQAUEQZ-UHFFFAOYSA-N 0.000 abstract 2
- 239000004014 plasticizer Substances 0.000 abstract 2
- 229920001084 poly(chloroprene) Polymers 0.000 abstract 2
- 239000004848 polyfunctional curative Substances 0.000 abstract 2
- 229920000642 polymer Polymers 0.000 abstract 2
- 229920001296 polysiloxane Polymers 0.000 abstract 2
- 229920002635 polyurethane Polymers 0.000 abstract 2
- 239000004814 polyurethane Substances 0.000 abstract 2
- 150000004760 silicates Chemical class 0.000 abstract 2
- 229920003048 styrene butadiene rubber Polymers 0.000 abstract 2
- 150000004763 sulfides Chemical class 0.000 abstract 2
- 239000004094 surface-active agent Substances 0.000 abstract 2
- 239000002966 varnish Substances 0.000 abstract 2
- 235000015112 vegetable and seed oil Nutrition 0.000 abstract 2
- 239000008158 vegetable oil Substances 0.000 abstract 2
- 239000011701 zinc Substances 0.000 abstract 2
- 229910052725 zinc Inorganic materials 0.000 abstract 2
- YMMIRJGHLJAYIC-UHFFFAOYSA-N 2,4,5-tris(ethenyl)-1,3-dioxolane Chemical compound C=CC1OC(C=C)C(C=C)O1 YMMIRJGHLJAYIC-UHFFFAOYSA-N 0.000 abstract 1
- XYWKQWRBBDPBCE-UHFFFAOYSA-N 2-butyl-4-ethenyl-5-prop-1-en-2-yl-1,3-dioxolane Chemical compound C(=C)(C)C1OC(OC1C=C)CCCC XYWKQWRBBDPBCE-UHFFFAOYSA-N 0.000 abstract 1
- XXJBQMRIEYKPFZ-UHFFFAOYSA-N 2-methylhexa-1,5-diene-3,4-diol Chemical compound C(=C)C(C(C(=C)C)O)O XXJBQMRIEYKPFZ-UHFFFAOYSA-N 0.000 abstract 1
- 230000002378 acidificating effect Effects 0.000 abstract 1
- 150000001299 aldehydes Chemical class 0.000 abstract 1
- 230000001680 brushing effect Effects 0.000 abstract 1
- 239000000919 ceramic Substances 0.000 abstract 1
- 150000002009 diols Chemical class 0.000 abstract 1
- 238000007598 dipping method Methods 0.000 abstract 1
- 239000004744 fabric Substances 0.000 abstract 1
- 238000005194 fractionation Methods 0.000 abstract 1
- 239000011521 glass Substances 0.000 abstract 1
- KUQWZSZYIQGTHT-UHFFFAOYSA-N hexa-1,5-diene-3,4-diol Chemical compound C=CC(O)C(O)C=C KUQWZSZYIQGTHT-UHFFFAOYSA-N 0.000 abstract 1
- 239000010985 leather Substances 0.000 abstract 1
- 238000006386 neutralization reaction Methods 0.000 abstract 1
- 239000005012 oleoresinous Substances 0.000 abstract 1
- HGBOYTHUEUWSSQ-UHFFFAOYSA-N pentanal Chemical compound CCCCC=O HGBOYTHUEUWSSQ-UHFFFAOYSA-N 0.000 abstract 1
- 238000000746 purification Methods 0.000 abstract 1
- 238000005507 spraying Methods 0.000 abstract 1
- 239000002023 wood Substances 0.000 abstract 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
- C09D137/00—Coating compositions based on homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a heterocyclic ring containing oxygen; Coating compositions based on derivatives of such polymers
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D317/00—Heterocyclic compounds containing five-membered rings having two oxygen atoms as the only ring hetero atoms
- C07D317/08—Heterocyclic compounds containing five-membered rings having two oxygen atoms as the only ring hetero atoms having the hetero atoms in positions 1 and 3
- C07D317/10—Heterocyclic compounds containing five-membered rings having two oxygen atoms as the only ring hetero atoms having the hetero atoms in positions 1 and 3 not condensed with other rings
- C07D317/12—Heterocyclic compounds containing five-membered rings having two oxygen atoms as the only ring hetero atoms having the hetero atoms in positions 1 and 3 not condensed with other rings with only hydrogen atoms or radicals containing only hydrogen and carbon atoms, directly attached to ring carbon atoms
-
- 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
- C08F24/00—Homopolymers and copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a heterocyclic ring containing oxygen
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Materials Engineering (AREA)
- Wood Science & Technology (AREA)
- Engineering & Computer Science (AREA)
- Life Sciences & Earth Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Paints Or Removers (AREA)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
- Compositions Of Macromolecular Compounds (AREA)
Abstract
Un procedimiento para preparar una composición formadora de película de secado al aire, caracterizado porque un secador de cobalto es mezclado con un dioxolano insaturado que tiene la fórmula estructural: **FIGURA** en la cual R es un radical de la clase que consiste de vinilo e isopropenilo; R1 es un radical de la clase que consiste de hidrógeno, vinilo, propenilo, isopropenilo, beta-fenilvinil, beta-(2-furil)-vinilo, fenilo, 2-furilo y bicicloheptadienilo, y R2 es un radical de la clase que consiste de alquilo saturado C1-C9 alquilo, vinilo, propenilo, isopropenilo, beta-fenilvinilo, beta-(2-furil)-vinilo, fenilo, tetrahidrofenilo bicicloheptadienilo, 2-furilo, dihidropiranilo, y dicloroetilo, por lo menos uno de los radicales R1 y R2 tienen un radical de la clase que consiste de vinilo e isopropenilo con lo cual se obtiene una composición formadora de película conteniendo como componente formador de la película único o esencial dicho dioxolano no saturado.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US852630A US3055766A (en) | 1959-11-13 | 1959-11-13 | Air drying, film forming compositions |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| ES262036A1 true ES262036A1 (es) | 1961-01-01 |
Family
ID=25313834
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ES0262036A Expired ES262036A1 (es) | 1959-11-13 | 1960-10-27 | Procedimiento para la preparar una composiciën formadora de pelicula de secado al aire |
Country Status (6)
| Country | Link |
|---|---|
| US (1) | US3055766A (es) |
| BE (1) | BE595703A (es) |
| DE (1) | DE1148033B (es) |
| ES (1) | ES262036A1 (es) |
| GB (1) | GB916563A (es) |
| NL (1) | NL257544A (es) |
Families Citing this family (14)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE1258002B (de) | 1961-11-20 | 1968-01-04 | Werk Fuer Bauelemente Der Nach | Verwendung von fluessigen oder festen Polydioxolanen zur Verbesserung der Verlaufeigenschaften und der Dauerwaermebestaendigkeit von Lacken |
| GB1095939A (en) * | 1963-09-27 | 1967-12-20 | Ici Ltd | Polymerisable compositions |
| US3417062A (en) * | 1966-07-11 | 1968-12-17 | Dow Chemical Co | 2-alkenyl-1,3-dioxolenium and 1,3-dioxenium salts and polymers thereof |
| US3936470A (en) * | 1975-01-27 | 1976-02-03 | Janssen Pharmaceutica N.V. | 1,3-Dioxolan-2-ylmethylimidazoles |
| US4483967A (en) * | 1981-08-07 | 1984-11-20 | The Procter & Gamble Company | Method of catalyzing oxygen-initiated free-radical polymerization and catalysts used therein |
| US4427835A (en) | 1981-08-07 | 1984-01-24 | The Procter & Gamble Company | Agents for preparing cross-linked polymers and paint and plastic compositions containing those agents |
| US4395361A (en) * | 1981-08-07 | 1983-07-26 | The Procter & Gamble Company | Catalysts for oxygen-initiated free-radical polymerization reactions |
| US4506048A (en) * | 1981-08-07 | 1985-03-19 | The Procter & Gamble Company | Agents for preparing cross-linked polymers and paint and plastic compositions containing those agents |
| US6300457B1 (en) | 1996-09-23 | 2001-10-09 | Foster Miller, Inc. | Polyester/polyurethane vinyl dioxolane based coating compositions |
| US7378457B2 (en) * | 2000-02-15 | 2008-05-27 | Foster Miller, Inc. | No VOC radiation curable resin compositions with enhanced flexibility |
| WO2002008298A1 (en) * | 2000-07-25 | 2002-01-31 | Foster-Miller, Inc. | Enzyme degradable curable resin compositions |
| FR2912149B1 (fr) * | 2007-02-05 | 2012-10-12 | Rhodia Poliamida E Especialidades Ltda | Utilisation de derives de dioxolane dans des systemes de revetement et formulation de systeme de revetement |
| FR2949478B1 (fr) * | 2009-09-03 | 2011-09-02 | Rhodia Poliamida E Especialidades Ltda | Compositions de finissage du cuir comprenant des derives de dioxolane |
| EP2524959B1 (de) * | 2011-05-17 | 2014-01-22 | Symrise AG | Riech- und/oder Aromastoffkompositionen enthaltend Dioxolane |
Family Cites Families (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CA515737A (en) * | 1955-08-16 | General Mills | Drying oil condensate with benzodioxane | |
| US2578861A (en) * | 1949-07-26 | 1951-12-18 | American Cyanamid Co | Unsaturated dioxolane compounds, products prepared therefrom, and methods of preparation |
| US2856309A (en) * | 1955-02-15 | 1958-10-14 | Exxon Research Engineering Co | Unsaturated hydrocarbon drying oils containing a hardening agent and a process of making them |
| US2862007A (en) * | 1957-09-27 | 1958-11-25 | Union Carbide Corp | Triply unsaturated 1,3-dioxolanes and process for their preparation |
-
0
- BE BE595703D patent/BE595703A/xx unknown
- NL NL257544D patent/NL257544A/xx unknown
-
1959
- 1959-11-13 US US852630A patent/US3055766A/en not_active Expired - Lifetime
-
1960
- 1960-10-05 GB GB34124/60A patent/GB916563A/en not_active Expired
- 1960-10-11 DE DEP25825A patent/DE1148033B/de active Pending
- 1960-10-27 ES ES0262036A patent/ES262036A1/es not_active Expired
Also Published As
| Publication number | Publication date |
|---|---|
| NL257544A (es) | |
| US3055766A (en) | 1962-09-25 |
| BE595703A (es) | |
| GB916563A (en) | 1963-01-23 |
| DE1148033B (de) | 1963-05-02 |
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