NO115064B - - Google Patents
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- Publication number
- NO115064B NO115064B NO153387A NO15338764A NO115064B NO 115064 B NO115064 B NO 115064B NO 153387 A NO153387 A NO 153387A NO 15338764 A NO15338764 A NO 15338764A NO 115064 B NO115064 B NO 115064B
- Authority
- NO
- Norway
- Prior art keywords
- polymers
- approx
- radical
- acid
- acid number
- Prior art date
Links
- 229920000642 polymer Polymers 0.000 claims description 38
- 239000002253 acid Substances 0.000 claims description 29
- 239000011248 coating agent Substances 0.000 claims description 29
- 239000000178 monomer Substances 0.000 claims description 22
- 238000000034 method Methods 0.000 claims description 16
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 claims description 10
- -1 glycidyl ester Chemical class 0.000 claims description 10
- 125000004432 carbon atom Chemical group C* 0.000 claims description 8
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical group [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims description 7
- 238000004519 manufacturing process Methods 0.000 claims description 7
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 claims description 6
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 claims description 5
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims description 5
- 125000004435 hydrogen atom Chemical class [H]* 0.000 claims description 5
- 229910052739 hydrogen Inorganic materials 0.000 claims description 3
- 239000001257 hydrogen Substances 0.000 claims description 3
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 3
- 229930195734 saturated hydrocarbon Natural products 0.000 claims description 3
- 125000003011 styrenyl group Chemical group [H]\C(*)=C(/[H])C1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 claims description 2
- 230000000379 polymerizing effect Effects 0.000 claims 1
- 239000000203 mixture Substances 0.000 description 30
- 238000009835 boiling Methods 0.000 description 23
- 229920001577 copolymer Polymers 0.000 description 20
- 238000000576 coating method Methods 0.000 description 16
- 239000007787 solid Substances 0.000 description 15
- 150000003254 radicals Chemical group 0.000 description 14
- 239000000047 product Substances 0.000 description 9
- 239000000463 material Substances 0.000 description 8
- 239000003054 catalyst Substances 0.000 description 7
- 239000002904 solvent Substances 0.000 description 7
- 230000032050 esterification Effects 0.000 description 6
- 238000005886 esterification reaction Methods 0.000 description 6
- 238000002156 mixing Methods 0.000 description 6
- 229920005989 resin Polymers 0.000 description 6
- 239000011347 resin Substances 0.000 description 6
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 5
- 238000010438 heat treatment Methods 0.000 description 5
- 239000008096 xylene Substances 0.000 description 5
- 229920003180 amino resin Polymers 0.000 description 4
- 239000004576 sand Substances 0.000 description 4
- 239000000126 substance Substances 0.000 description 4
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 3
- 239000004925 Acrylic resin Substances 0.000 description 3
- 229920000178 Acrylic resin Polymers 0.000 description 3
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 3
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 3
- 125000003055 glycidyl group Chemical group C(C1CO1)* 0.000 description 3
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 3
- 239000004615 ingredient Substances 0.000 description 3
- 229920001568 phenolic resin Polymers 0.000 description 3
- 230000000704 physical effect Effects 0.000 description 3
- 239000002685 polymerization catalyst Substances 0.000 description 3
- 239000011541 reaction mixture Substances 0.000 description 3
- 238000010992 reflux Methods 0.000 description 3
- KXGFMDJXCMQABM-UHFFFAOYSA-N 2-methoxy-6-methylphenol Chemical compound [CH]OC1=CC=CC([CH])=C1O KXGFMDJXCMQABM-UHFFFAOYSA-N 0.000 description 2
- BRLQWZUYTZBJKN-UHFFFAOYSA-N Epichlorohydrin Chemical compound ClCC1CO1 BRLQWZUYTZBJKN-UHFFFAOYSA-N 0.000 description 2
- 239000004593 Epoxy Substances 0.000 description 2
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerol Natural products OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 2
- 239000004721 Polyphenylene oxide Substances 0.000 description 2
- 230000002378 acidificating effect Effects 0.000 description 2
- 150000007513 acids Chemical class 0.000 description 2
- 150000001735 carboxylic acids Chemical class 0.000 description 2
- 229940072282 cardura Drugs 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
- 150000001875 compounds Chemical class 0.000 description 2
- 210000003298 dental enamel Anatomy 0.000 description 2
- RUZYUOTYCVRMRZ-UHFFFAOYSA-N doxazosin Chemical compound C1OC2=CC=CC=C2OC1C(=O)N(CC1)CCN1C1=NC(N)=C(C=C(C(OC)=C2)OC)C2=N1 RUZYUOTYCVRMRZ-UHFFFAOYSA-N 0.000 description 2
- 125000004185 ester group Chemical group 0.000 description 2
- 150000002148 esters Chemical class 0.000 description 2
- 238000000227 grinding Methods 0.000 description 2
- 238000009998 heat setting Methods 0.000 description 2
- 239000012535 impurity Substances 0.000 description 2
- KQNPFQTWMSNSAP-UHFFFAOYSA-N isobutyric acid Chemical compound CC(C)C(O)=O KQNPFQTWMSNSAP-UHFFFAOYSA-N 0.000 description 2
- 239000002184 metal Substances 0.000 description 2
- 229910052751 metal Inorganic materials 0.000 description 2
- 239000002245 particle Substances 0.000 description 2
- 229920000570 polyether Polymers 0.000 description 2
- 238000006116 polymerization reaction Methods 0.000 description 2
- 238000002360 preparation method Methods 0.000 description 2
- 150000003839 salts Chemical class 0.000 description 2
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 2
- 229920002554 vinyl polymer Polymers 0.000 description 2
- PAOHAQSLJSMLAT-UHFFFAOYSA-N 1-butylperoxybutane Chemical group CCCCOOCCCC PAOHAQSLJSMLAT-UHFFFAOYSA-N 0.000 description 1
- IKNDGHRNXGEHTO-UHFFFAOYSA-N 2,2-dimethyloctanoic acid Chemical compound CCCCCCC(C)(C)C(O)=O IKNDGHRNXGEHTO-UHFFFAOYSA-N 0.000 description 1
- JAHNSTQSQJOJLO-UHFFFAOYSA-N 2-(3-fluorophenyl)-1h-imidazole Chemical compound FC1=CC=CC(C=2NC=CN=2)=C1 JAHNSTQSQJOJLO-UHFFFAOYSA-N 0.000 description 1
- GGYSTYGPXYUWTQ-UHFFFAOYSA-N 2-ethyl-2-methyltetradecanoic acid Chemical compound CCCCCCCCCCCCC(C)(CC)C(O)=O GGYSTYGPXYUWTQ-UHFFFAOYSA-N 0.000 description 1
- FRIBMENBGGCKPD-UHFFFAOYSA-N 3-(2,3-dimethoxyphenyl)prop-2-enal Chemical group COC1=CC=CC(C=CC=O)=C1OC FRIBMENBGGCKPD-UHFFFAOYSA-N 0.000 description 1
- YCIGYTFKOXGYTA-UHFFFAOYSA-N 4-(3-cyanopropyldiazenyl)butanenitrile Chemical group N#CCCCN=NCCCC#N YCIGYTFKOXGYTA-UHFFFAOYSA-N 0.000 description 1
- GZVHEAJQGPRDLQ-UHFFFAOYSA-N 6-phenyl-1,3,5-triazine-2,4-diamine Chemical compound NC1=NC(N)=NC(C=2C=CC=CC=2)=N1 GZVHEAJQGPRDLQ-UHFFFAOYSA-N 0.000 description 1
- NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 description 1
- SEBXPTHGJDDBPO-UHFFFAOYSA-N C(C1=CC=CC=C1)S(=O)(=O)N.N1=C(N)N=C(N)N=C1N Chemical compound C(C1=CC=CC=C1)S(=O)(=O)N.N1=C(N)N=C(N)N=C1N SEBXPTHGJDDBPO-UHFFFAOYSA-N 0.000 description 1
- 229920000877 Melamine resin Polymers 0.000 description 1
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 description 1
- VVQNEPGJFQJSBK-UHFFFAOYSA-N Methyl methacrylate Chemical group COC(=O)C(C)=C VVQNEPGJFQJSBK-UHFFFAOYSA-N 0.000 description 1
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 1
- 241000208125 Nicotiana Species 0.000 description 1
- 235000002637 Nicotiana tabacum Nutrition 0.000 description 1
- OFOBLEOULBTSOW-UHFFFAOYSA-N Propanedioic acid Natural products OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 1
- VBIIFPGSPJYLRR-UHFFFAOYSA-M Stearyltrimethylammonium chloride Chemical compound [Cl-].CCCCCCCCCCCCCCCCCC[N+](C)(C)C VBIIFPGSPJYLRR-UHFFFAOYSA-M 0.000 description 1
- GSEJCLTVZPLZKY-UHFFFAOYSA-N Triethanolamine Chemical compound OCCN(CCO)CCO GSEJCLTVZPLZKY-UHFFFAOYSA-N 0.000 description 1
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 1
- 150000001252 acrylic acid derivatives Chemical class 0.000 description 1
- 125000001931 aliphatic group Chemical group 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- KXHPPCXNWTUNSB-UHFFFAOYSA-M benzyl(trimethyl)azanium;chloride Chemical compound [Cl-].C[N+](C)(C)CC1=CC=CC=C1 KXHPPCXNWTUNSB-UHFFFAOYSA-M 0.000 description 1
- NDKBVBUGCNGSJJ-UHFFFAOYSA-M benzyltrimethylammonium hydroxide Chemical compound [OH-].C[N+](C)(C)CC1=CC=CC=C1 NDKBVBUGCNGSJJ-UHFFFAOYSA-M 0.000 description 1
- IISBACLAFKSPIT-UHFFFAOYSA-N bisphenol A Chemical compound C=1C=C(O)C=CC=1C(C)(C)C1=CC=C(O)C=C1 IISBACLAFKSPIT-UHFFFAOYSA-N 0.000 description 1
- 239000004202 carbamide Substances 0.000 description 1
- 150000001732 carboxylic acid derivatives Chemical class 0.000 description 1
- 239000007795 chemical reaction product Substances 0.000 description 1
- 239000012459 cleaning agent Substances 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 238000005260 corrosion Methods 0.000 description 1
- 230000007797 corrosion Effects 0.000 description 1
- 239000003431 cross linking reagent Substances 0.000 description 1
- 229940079593 drug Drugs 0.000 description 1
- 239000003814 drug Substances 0.000 description 1
- 238000007590 electrostatic spraying Methods 0.000 description 1
- 239000000945 filler Substances 0.000 description 1
- 239000012467 final product Substances 0.000 description 1
- 238000010304 firing Methods 0.000 description 1
- 125000005456 glyceride group Chemical group 0.000 description 1
- 238000007654 immersion Methods 0.000 description 1
- 239000012442 inert solvent Substances 0.000 description 1
- 230000002045 lasting effect Effects 0.000 description 1
- 239000000314 lubricant Substances 0.000 description 1
- VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 description 1
- 239000011976 maleic acid Substances 0.000 description 1
- FPYJFEHAWHCUMM-UHFFFAOYSA-N maleic anhydride Chemical compound O=C1OC(=O)C=C1 FPYJFEHAWHCUMM-UHFFFAOYSA-N 0.000 description 1
- JDSHMPZPIAZGSV-UHFFFAOYSA-N melamine Chemical compound NC1=NC(N)=NC(N)=N1 JDSHMPZPIAZGSV-UHFFFAOYSA-N 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 150000002734 metacrylic acid derivatives Chemical class 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- JYVLIDXNZAXMDK-UHFFFAOYSA-N methyl propyl carbinol Natural products CCCC(C)O JYVLIDXNZAXMDK-UHFFFAOYSA-N 0.000 description 1
- LVHBHZANLOWSRM-UHFFFAOYSA-N methylenebutanedioic acid Natural products OC(=O)CC(=C)C(O)=O LVHBHZANLOWSRM-UHFFFAOYSA-N 0.000 description 1
- 239000003607 modifier Substances 0.000 description 1
- 150000002762 monocarboxylic acid derivatives Chemical class 0.000 description 1
- 235000015097 nutrients Nutrition 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 239000004014 plasticizer Substances 0.000 description 1
- HJWLCRVIBGQPNF-UHFFFAOYSA-N prop-2-enylbenzene Chemical compound C=CCC1=CC=CC=C1 HJWLCRVIBGQPNF-UHFFFAOYSA-N 0.000 description 1
- 230000035484 reaction time Effects 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 238000009991 scouring Methods 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 238000010186 staining Methods 0.000 description 1
- 239000000758 substrate Substances 0.000 description 1
- 229920001187 thermosetting polymer Polymers 0.000 description 1
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
Classifications
-
- 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
- C08F22/00—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 carboxyl radical and containing at least one other carboxyl radical in the molecule; Salts, anhydrides, esters, amides, imides or nitriles thereof
-
- 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
- C08F20/00—Homopolymers and copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and only one being terminated by only one carboxyl radical or a salt, anhydride, ester, amide, imide or nitrile thereof
- C08F20/62—Monocarboxylic acids having ten or more carbon atoms; Derivatives thereof
-
- 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
- C08F8/00—Chemical modification by after-treatment
- C08F8/14—Esterification
-
- 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
- C09D135/00—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 carboxyl radical, and containing at least another carboxyl radical in the molecule, or of salts, anhydrides, esters, amides, imides or nitriles thereof; Coating compositions based on derivatives of such polymers
- C09D135/02—Homopolymers or copolymers of esters
-
- 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
- C09D161/00—Coating compositions based on condensation polymers of aldehydes or ketones; Coating compositions based on derivatives of such polymers
- C09D161/20—Condensation polymers of aldehydes or ketones with only compounds containing hydrogen attached to nitrogen
-
- 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
- C09D163/00—Coating compositions based on epoxy resins; Coating compositions based on derivatives of epoxy resins
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Wood Science & Technology (AREA)
- Engineering & Computer Science (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Life Sciences & Earth Sciences (AREA)
- Materials Engineering (AREA)
- General Chemical & Material Sciences (AREA)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
- Paints Or Removers (AREA)
- Polyoxymethylene Polymers And Polymers With Carbon-To-Carbon Bonds (AREA)
- Macromolecular Compounds Obtained By Forming Nitrogen-Containing Linkages In General (AREA)
- Compositions Of Macromolecular Compounds (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US28358963A | 1963-05-27 | 1963-05-27 | |
| US31375963A | 1963-10-04 | 1963-10-04 | |
| US364285A US3330814A (en) | 1963-05-27 | 1964-05-01 | Hydroxyl-containing copolymers |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| NO115064B true NO115064B (de) | 1968-07-15 |
Family
ID=27403405
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| NO153387A NO115064B (de) | 1963-05-27 | 1964-05-26 |
Country Status (12)
| Country | Link |
|---|---|
| US (1) | US3330814A (de) |
| JP (1) | JPS4826386B1 (de) |
| BE (1) | BE648451A (de) |
| CH (1) | CH443690A (de) |
| DE (1) | DE1520610A1 (de) |
| ES (1) | ES300294A1 (de) |
| GB (1) | GB1009217A (de) |
| LU (1) | LU46110A1 (de) |
| MY (1) | MY6600142A (de) |
| NL (1) | NL6405830A (de) |
| NO (1) | NO115064B (de) |
| SE (1) | SE307855B (de) |
Families Citing this family (29)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3442873A (en) * | 1966-04-29 | 1969-05-06 | Du Pont | Novel polymers having pendent ester groups |
| GB1222369A (en) * | 1966-12-14 | 1971-02-10 | Nippon Paint Co Ltd | Polymerizable monomers and liquid coating compositions |
| DE1644822C3 (de) * | 1967-04-26 | 1973-09-13 | Basf Farben + Fasern Ag, 2000 Hamburg | Einbrennlacke |
| JPS4833015B1 (de) * | 1967-06-02 | 1973-10-11 | Nippon Paint Co Ltd | |
| US3547690A (en) * | 1968-04-16 | 1970-12-15 | Borden Inc | Process for controlling fabric hardness by impregnating with a latex |
| US3488215A (en) * | 1968-06-21 | 1970-01-06 | Nat Patent Dev Corp | Nonfogging transparent material |
| US3622651A (en) * | 1969-12-01 | 1971-11-23 | Du Pont | Novel polymer having pendent ester groups for low temperature bake coatings |
| JPS515423B1 (de) * | 1971-07-14 | 1976-02-19 | ||
| US3919146A (en) * | 1971-09-07 | 1975-11-11 | Rohm & Haas | Caulking composition comprising polymer having addition polymerized backbone having carboxyl groups esterified with drying oil fatty acid glycidyl ester |
| US4021504A (en) * | 1973-11-02 | 1977-05-03 | The Goodyear Tire & Rubber Company | Thermosetting coating composition of acrylic interpolymers |
| ZA744070B (en) * | 1974-06-25 | 1976-05-26 | Prolux Paint Mfg Pty | Film forming compositions and their preparation |
| DE2515705C2 (de) * | 1975-04-10 | 1982-12-30 | Hoechst Ag, 6000 Frankfurt | Verfahren zur Herstellung von in organischen Lösungsmitteln löslichen Copolymerisaten |
| US4101601A (en) * | 1975-12-24 | 1978-07-18 | Celanese Corporation | Epoxy-catalyst additive system to produce higher I.V. polybutylene terephthalate from low I.V. polymer |
| DE2603259C3 (de) * | 1976-01-29 | 1982-10-21 | Hoechst Ag, 6000 Frankfurt | Verfahren zur Herstellung von hydroxylgruppenenthaltenden Mischpolymerisaten |
| US4210702A (en) * | 1976-01-29 | 1980-07-01 | Hoechst Aktiengesellschaft | Process for the manufacture of soluble copolymers which contain hydroxyl groups and which copolymers can be crosslinked with organic polyisocyanates |
| DE2618810C3 (de) * | 1976-04-29 | 1978-12-07 | Hoechst Ag, 6000 Frankfurt | Verfahren zur Herstellung von Überzügen |
| NL7708218A (nl) * | 1977-07-23 | 1979-01-25 | Akzo Nv | Vloeibare bekledingssamenstelling met een hoog vaste-stofgehalte op basis van een acrylaat- copolymeer. |
| JPS543169B1 (de) * | 1977-10-12 | 1979-02-19 | ||
| US4363896A (en) * | 1980-01-04 | 1982-12-14 | Ford Motor Company | Composition with latent reactive catalyst-#4 |
| US4281075A (en) * | 1980-01-04 | 1981-07-28 | Ford Motor Company | Sulfonate ester catalysts in thermosetting compositions |
| US4323660A (en) * | 1980-01-04 | 1982-04-06 | Ford Motor Company | Composition with latent reactive catalyst - #5 |
| DE3022996C2 (de) * | 1980-06-20 | 1982-02-04 | Basf Farben + Fasern Ag, 2000 Hamburg | Einbrennlack |
| AT372096B (de) * | 1980-09-23 | 1983-08-25 | Vianova Kunstharz Ag | Verfahren zur herstellung von selbstvernetzenden copolymerisaten zur verwendung als bindemittel in einbrennlacken |
| US4555535A (en) * | 1984-03-07 | 1985-11-26 | E. I. Du Pont De Nemours And Company | Acrylic polyurethane coating composition |
| DE3415531A1 (de) * | 1984-04-26 | 1985-10-31 | Bayer Ag, 5090 Leverkusen | Verfahren zur herstellung von hydroxylgruppen aufweisenden alkoxylierungsprodukten von organischen carbonsaeuren und ihre verwendung zur herstellung von polyurethankunststoffen |
| US4988766A (en) * | 1987-05-13 | 1991-01-29 | Ppg Industries, Inc. | Polymers prepared by polymerizing alpha, beta-ethylenically unsaturated acids and epoxy compounds and crosslinked products therefrom |
| DE4415319A1 (de) * | 1994-05-02 | 1995-11-09 | Hoechst Ag | Hydroxy- und Carboxylgruppen enthaltende Copolymerisate, ihre Herstellung und ihre Verwendung in festkörperreichen Beschichtungsmitteln |
| DE4445355A1 (de) * | 1994-12-20 | 1996-06-27 | Herberts Gmbh | Bindemittel, diese enthaltende wäßrige und lösemittelhaltige Überzugsmittel, Verfahren zu deren Herstellung und zur Herstellung von Mehrschichtlackierungen |
| US20020156221A1 (en) * | 2001-02-20 | 2002-10-24 | Meyer Gerald Wayne | High solids acrylic resin |
Family Cites Families (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2819237A (en) * | 1953-09-22 | 1958-01-07 | American Cyanamid Co | Aqueous dispersions of a copolymer of an ethylenically unsaturated monomer containing a primary hydroxy group and a thermosetting resin forming reaction product |
| US2957853A (en) * | 1956-06-20 | 1960-10-25 | Monsanto Chemicals | Terpolymer systems containing carboxyl groups and hydroxyl groups |
| NL216714A (de) * | 1956-06-25 | |||
| US2966479A (en) * | 1957-09-27 | 1960-12-27 | Shell Oil Co | Process for preparing high molecular weight polyesters from monoepoxides |
| NL245932A (de) * | 1960-05-18 |
-
1964
- 1964-05-01 US US364285A patent/US3330814A/en not_active Expired - Lifetime
- 1964-05-11 GB GB19580/64A patent/GB1009217A/en not_active Expired
- 1964-05-15 DE DE19641520610 patent/DE1520610A1/de active Pending
- 1964-05-19 LU LU46110D patent/LU46110A1/xx unknown
- 1964-05-21 JP JP39028411A patent/JPS4826386B1/ja active Pending
- 1964-05-25 CH CH679664A patent/CH443690A/de unknown
- 1964-05-25 NL NL6405830A patent/NL6405830A/xx unknown
- 1964-05-26 SE SE6370/64A patent/SE307855B/xx unknown
- 1964-05-26 ES ES300294A patent/ES300294A1/es not_active Expired
- 1964-05-26 NO NO153387A patent/NO115064B/no unknown
- 1964-05-27 BE BE648451D patent/BE648451A/xx unknown
-
1966
- 1966-12-31 MY MY1966142A patent/MY6600142A/xx unknown
Also Published As
| Publication number | Publication date |
|---|---|
| GB1009217A (en) | 1965-11-10 |
| US3330814A (en) | 1967-07-11 |
| SE307855B (de) | 1969-01-20 |
| BE648451A (de) | 1964-11-27 |
| CH443690A (de) | 1967-09-15 |
| NL6405830A (de) | 1964-11-30 |
| ES300294A1 (es) | 1964-11-16 |
| MY6600142A (en) | 1966-12-31 |
| LU46110A1 (de) | 1972-01-01 |
| DE1520610A1 (de) | 1969-04-10 |
| JPS4826386B1 (de) | 1973-08-09 |
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