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)
- Life Sciences & Earth Sciences (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Wood Science & Technology (AREA)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Paints Or Removers (AREA)
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 (en, 2012) |
| BE (1) | BE595703A (en, 2012) |
| DE (1) | DE1148033B (en, 2012) |
| ES (1) | ES262036A1 (en, 2012) |
| GB (1) | GB916563A (en, 2012) |
| NL (1) | NL257544A (en, 2012) |
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 |
| 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 |
| US4483967A (en) * | 1981-08-07 | 1984-11-20 | The Procter & Gamble Company | Method of catalyzing oxygen-initiated free-radical polymerization and catalysts used therein |
| 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 |
| US4395361A (en) | 1981-08-07 | 1983-07-26 | The Procter & Gamble Company | Catalysts for oxygen-initiated free-radical polymerization reactions |
| 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
- NL NL257544D patent/NL257544A/xx unknown
- BE BE595703D patent/BE595703A/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 |
|---|---|
| DE1148033B (de) | 1963-05-02 |
| BE595703A (en, 2012) | |
| GB916563A (en) | 1963-01-23 |
| NL257544A (en, 2012) | |
| US3055766A (en) | 1962-09-25 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| ES262036A1 (es) | Procedimiento para la preparar una composiciën formadora de pelicula de secado al aire | |
| EP0015147A1 (en) | Lithographic ink containing oxidatively curable reactive diluent and use thereof | |
| US4253397A (en) | Method of printing with lithographic ink of reduced volatile solvent content for reducing atmospheric pollution | |
| GB847421A (en) | Improvements in or relating to synthetic resin coating compositions | |
| CA2120589A1 (en) | Alkaline earth metal salts, transition metal salts and transition metal complexes of ketocarboxylic acids as corrosion inhibitors | |
| US3245927A (en) | Coating compositions containing cyclic acetals | |
| US2961331A (en) | Drier compositions | |
| GB819177A (en) | Coating compositions and production of coatings therefrom | |
| NO139464B (no) | Fallsikring for sikringstau. | |
| US4089690A (en) | Corrosion inhibiting coatings for steel | |
| CA1060763A (en) | Coating compositions | |
| KR100355315B1 (ko) | 모르폴린유도체와케토카르복실산과의착물 | |
| US2995532A (en) | Corrosion preventive composition | |
| GB726694A (en) | Synthetic resinous compositions for coating metals | |
| CN105199480B (zh) | 一种光固化阻焊油墨组合物 | |
| ES259034A1 (es) | Mejoras introducidas en la preparaciën de adiciones para composiciones de revestimiento | |
| US2197813A (en) | Synthetic drying oil anx methob of | |
| Gardner | Paint technology and tests | |
| EP3507280A2 (en) | Coalescing agent derived from dioxolane derivatives | |
| CN115612227A (zh) | 一种pvc制品及其制备方法 | |
| US2631944A (en) | Organic driers in organic film forming compositions | |
| US2398069A (en) | Antifouling composition | |
| US2894849A (en) | Alpha, gamma diketones in combination with metallo-organic driers as drying accelerators for siccative coatings | |
| US1920160A (en) | Coating composition containing a siccative | |
| US2486664A (en) | Rustproof coating of ferrous metals |