EP1587870A1 - Use of melamine resin foils and/or films for coating three-dimensionally structured surfaces and/or moulded bodies - Google Patents
Use of melamine resin foils and/or films for coating three-dimensionally structured surfaces and/or moulded bodiesInfo
- Publication number
- EP1587870A1 EP1587870A1 EP04701297A EP04701297A EP1587870A1 EP 1587870 A1 EP1587870 A1 EP 1587870A1 EP 04701297 A EP04701297 A EP 04701297A EP 04701297 A EP04701297 A EP 04701297A EP 1587870 A1 EP1587870 A1 EP 1587870A1
- Authority
- EP
- European Patent Office
- Prior art keywords
- melamine
- weight
- coating
- iii
- films
- 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- Withdrawn
Links
- 229920000877 Melamine resin Polymers 0.000 title claims abstract description 76
- 239000004640 Melamine resin Substances 0.000 title claims abstract description 42
- 239000011248 coating agent Substances 0.000 title claims abstract description 32
- 238000000576 coating method Methods 0.000 title claims abstract description 32
- 239000011888 foil Substances 0.000 title abstract description 4
- IVJISJACKSSFGE-UHFFFAOYSA-N formaldehyde;1,3,5-triazine-2,4,6-triamine Chemical compound O=C.NC1=NC(N)=NC(N)=N1 IVJISJACKSSFGE-UHFFFAOYSA-N 0.000 claims abstract description 27
- 239000002657 fibrous material Substances 0.000 claims abstract description 12
- 239000007864 aqueous solution Substances 0.000 claims abstract description 11
- 239000001913 cellulose Substances 0.000 claims abstract description 11
- 229920002678 cellulose Polymers 0.000 claims abstract description 11
- 239000004815 dispersion polymer Substances 0.000 claims abstract description 9
- 239000000203 mixture Substances 0.000 claims description 28
- 229920005989 resin Polymers 0.000 claims description 16
- 239000011347 resin Substances 0.000 claims description 16
- 239000007859 condensation product Substances 0.000 claims description 15
- 229920001577 copolymer Polymers 0.000 claims description 11
- 239000000463 material Substances 0.000 claims description 11
- 229920003002 synthetic resin Polymers 0.000 claims description 11
- 239000000057 synthetic resin Substances 0.000 claims description 11
- 239000006185 dispersion Substances 0.000 claims description 7
- 239000007788 liquid Substances 0.000 claims description 7
- 238000000034 method Methods 0.000 claims description 6
- 238000000465 moulding Methods 0.000 claims description 6
- 239000002023 wood Substances 0.000 claims description 6
- 229920001807 Urea-formaldehyde Polymers 0.000 claims description 4
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims description 4
- 125000003055 glycidyl group Chemical group C(C1CO1)* 0.000 claims description 4
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims description 4
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 claims description 3
- 239000004202 carbamide Substances 0.000 claims description 3
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 claims description 3
- 150000001252 acrylic acid derivatives Chemical class 0.000 claims description 2
- 238000006482 condensation reaction Methods 0.000 claims description 2
- AVXURJPOCDRRFD-UHFFFAOYSA-N Hydroxylamine Chemical compound ON AVXURJPOCDRRFD-UHFFFAOYSA-N 0.000 claims 2
- HANVTCGOAROXMV-UHFFFAOYSA-N formaldehyde;1,3,5-triazine-2,4,6-triamine;urea Chemical compound O=C.NC(N)=O.NC1=NC(N)=NC(N)=N1 HANVTCGOAROXMV-UHFFFAOYSA-N 0.000 claims 1
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 18
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical group OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 16
- 238000004519 manufacturing process Methods 0.000 description 9
- 239000000123 paper Substances 0.000 description 8
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 5
- 239000000853 adhesive Substances 0.000 description 5
- 239000000178 monomer Substances 0.000 description 5
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 4
- 125000000524 functional group Chemical group 0.000 description 4
- 239000004848 polyfunctional curative Substances 0.000 description 4
- 239000011148 porous material Substances 0.000 description 4
- 238000003825 pressing Methods 0.000 description 4
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- 230000001070 adhesive effect Effects 0.000 description 3
- -1 carbonyl - Chemical class 0.000 description 3
- 238000009833 condensation Methods 0.000 description 3
- 230000005494 condensation Effects 0.000 description 3
- 239000004744 fabric Substances 0.000 description 3
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 3
- JDSHMPZPIAZGSV-UHFFFAOYSA-N melamine Chemical compound NC1=NC(N)=NC(N)=N1 JDSHMPZPIAZGSV-UHFFFAOYSA-N 0.000 description 3
- 239000007787 solid Substances 0.000 description 3
- 239000000243 solution Substances 0.000 description 3
- 229920001169 thermoplastic Polymers 0.000 description 3
- 239000004416 thermosoftening plastic Substances 0.000 description 3
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 2
- KAKZBPTYRLMSJV-UHFFFAOYSA-N Butadiene Chemical compound C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 description 2
- SOGAXMICEFXMKE-UHFFFAOYSA-N Butylmethacrylate Chemical compound CCCCOC(=O)C(C)=C SOGAXMICEFXMKE-UHFFFAOYSA-N 0.000 description 2
- VZCYOOQTPOCHFL-OWOJBTEDSA-N Fumaric acid Chemical compound OC(=O)\C=C\C(O)=O VZCYOOQTPOCHFL-OWOJBTEDSA-N 0.000 description 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 2
- RRHGJUQNOFWUDK-UHFFFAOYSA-N Isoprene Chemical compound CC(=C)C=C RRHGJUQNOFWUDK-UHFFFAOYSA-N 0.000 description 2
- BAPJBEWLBFYGME-UHFFFAOYSA-N Methyl acrylate Chemical compound COC(=O)C=C BAPJBEWLBFYGME-UHFFFAOYSA-N 0.000 description 2
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 2
- 239000000654 additive Substances 0.000 description 2
- 239000002313 adhesive film Substances 0.000 description 2
- 125000005907 alkyl ester group Chemical group 0.000 description 2
- 150000001408 amides Chemical class 0.000 description 2
- CDQSJQSWAWPGKG-UHFFFAOYSA-N butane-1,1-diol Chemical compound CCCC(O)O CDQSJQSWAWPGKG-UHFFFAOYSA-N 0.000 description 2
- 238000012512 characterization method Methods 0.000 description 2
- 150000001875 compounds Chemical class 0.000 description 2
- 238000004821 distillation Methods 0.000 description 2
- JBKVHLHDHHXQEQ-UHFFFAOYSA-N epsilon-caprolactam Chemical compound O=C1CCCCCN1 JBKVHLHDHHXQEQ-UHFFFAOYSA-N 0.000 description 2
- BDAGIHXWWSANSR-UHFFFAOYSA-N methanoic acid Natural products OC=O BDAGIHXWWSANSR-UHFFFAOYSA-N 0.000 description 2
- 230000008961 swelling Effects 0.000 description 2
- 238000012360 testing method Methods 0.000 description 2
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 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
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- VZXTWGWHSMCWGA-UHFFFAOYSA-N 1,3,5-triazine-2,4-diamine Chemical compound NC1=NC=NC(N)=N1 VZXTWGWHSMCWGA-UHFFFAOYSA-N 0.000 description 1
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 1
- ZUAURMBNZUCEAF-UHFFFAOYSA-N 2-(2-phenoxyethoxy)ethanol Chemical compound OCCOCCOC1=CC=CC=C1 ZUAURMBNZUCEAF-UHFFFAOYSA-N 0.000 description 1
- 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 description 1
- GOXQRTZXKQZDDN-UHFFFAOYSA-N 2-Ethylhexyl acrylate Chemical compound CCCCC(CC)COC(=O)C=C GOXQRTZXKQZDDN-UHFFFAOYSA-N 0.000 description 1
- WDQMWEYDKDCEHT-UHFFFAOYSA-N 2-ethylhexyl 2-methylprop-2-enoate Chemical compound CCCCC(CC)COC(=O)C(C)=C WDQMWEYDKDCEHT-UHFFFAOYSA-N 0.000 description 1
- 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
- HRPVXLWXLXDGHG-UHFFFAOYSA-N Acrylamide Chemical compound NC(=O)C=C HRPVXLWXLXDGHG-UHFFFAOYSA-N 0.000 description 1
- NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 description 1
- NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 description 1
- JIGUQPWFLRLWPJ-UHFFFAOYSA-N Ethyl acrylate Chemical compound CCOC(=O)C=C JIGUQPWFLRLWPJ-UHFFFAOYSA-N 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 compound COC(=O)C(C)=C VVQNEPGJFQJSBK-UHFFFAOYSA-N 0.000 description 1
- GYCMBHHDWRMZGG-UHFFFAOYSA-N Methylacrylonitrile Chemical compound CC(=C)C#N GYCMBHHDWRMZGG-UHFFFAOYSA-N 0.000 description 1
- OFOBLEOULBTSOW-UHFFFAOYSA-N Propanedioic acid Natural products OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 1
- 229930006000 Sucrose Natural products 0.000 description 1
- CZMRCDWAGMRECN-UGDNZRGBSA-N Sucrose Chemical compound O[C@H]1[C@H](O)[C@@H](CO)O[C@@]1(CO)O[C@@H]1[C@H](O)[C@@H](O)[C@H](O)[C@@H](CO)O1 CZMRCDWAGMRECN-UGDNZRGBSA-N 0.000 description 1
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 1
- BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 description 1
- QYKIQEUNHZKYBP-UHFFFAOYSA-N Vinyl ether Chemical class C=COC=C QYKIQEUNHZKYBP-UHFFFAOYSA-N 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- XYLMUPLGERFSHI-UHFFFAOYSA-N alpha-Methylstyrene Chemical compound CC(=C)C1=CC=CC=C1 XYLMUPLGERFSHI-UHFFFAOYSA-N 0.000 description 1
- 229920003180 amino resin Polymers 0.000 description 1
- CQEYYJKEWSMYFG-UHFFFAOYSA-N butyl acrylate Chemical compound CCCCOC(=O)C=C CQEYYJKEWSMYFG-UHFFFAOYSA-N 0.000 description 1
- 125000004432 carbon atom Chemical group C* 0.000 description 1
- 239000003054 catalyst Substances 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 239000011093 chipboard Substances 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 239000002131 composite material Substances 0.000 description 1
- GMSCBRSQMRDRCD-UHFFFAOYSA-N dodecyl 2-methylprop-2-enoate Chemical compound CCCCCCCCCCCCOC(=O)C(C)=C GMSCBRSQMRDRCD-UHFFFAOYSA-N 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- UIWXSTHGICQLQT-UHFFFAOYSA-N ethenyl propanoate Chemical compound CCC(=O)OC=C UIWXSTHGICQLQT-UHFFFAOYSA-N 0.000 description 1
- SUPCQIBBMFXVTL-UHFFFAOYSA-N ethyl 2-methylprop-2-enoate Chemical compound CCOC(=O)C(C)=C SUPCQIBBMFXVTL-UHFFFAOYSA-N 0.000 description 1
- 238000011156 evaluation Methods 0.000 description 1
- 239000000835 fiber Substances 0.000 description 1
- 235000019253 formic acid Nutrition 0.000 description 1
- 239000001530 fumaric acid Substances 0.000 description 1
- 238000005470 impregnation Methods 0.000 description 1
- 239000004922 lacquer Substances 0.000 description 1
- PBOSTUDLECTMNL-UHFFFAOYSA-N lauryl acrylate Chemical compound CCCCCCCCCCCCOC(=O)C=C PBOSTUDLECTMNL-UHFFFAOYSA-N 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
- FQPSGWSUVKBHSU-UHFFFAOYSA-N methacrylamide Chemical compound CC(=C)C(N)=O FQPSGWSUVKBHSU-UHFFFAOYSA-N 0.000 description 1
- 125000005397 methacrylic acid ester group Chemical group 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 239000003607 modifier Substances 0.000 description 1
- 238000006386 neutralization reaction Methods 0.000 description 1
- 239000004745 nonwoven fabric Substances 0.000 description 1
- PNJWIWWMYCMZRO-UHFFFAOYSA-N pent‐4‐en‐2‐one Natural products CC(=O)CC=C PNJWIWWMYCMZRO-UHFFFAOYSA-N 0.000 description 1
- 230000000379 polymerizing effect Effects 0.000 description 1
- 238000012545 processing Methods 0.000 description 1
- HJWLCRVIBGQPNF-UHFFFAOYSA-N prop-2-enylbenzene Chemical compound C=CCC1=CC=CC=C1 HJWLCRVIBGQPNF-UHFFFAOYSA-N 0.000 description 1
- BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 description 1
- NHARPDSAXCBDDR-UHFFFAOYSA-N propyl 2-methylprop-2-enoate Chemical compound CCCOC(=O)C(C)=C NHARPDSAXCBDDR-UHFFFAOYSA-N 0.000 description 1
- PNXMTCDJUBJHQJ-UHFFFAOYSA-N propyl prop-2-enoate Chemical compound CCCOC(=O)C=C PNXMTCDJUBJHQJ-UHFFFAOYSA-N 0.000 description 1
- PYWVYCXTNDRMGF-UHFFFAOYSA-N rhodamine B Chemical compound [Cl-].C=12C=CC(=[N+](CC)CC)C=C2OC2=CC(N(CC)CC)=CC=C2C=1C1=CC=CC=C1C(O)=O PYWVYCXTNDRMGF-UHFFFAOYSA-N 0.000 description 1
- 229940043267 rhodamine b Drugs 0.000 description 1
- 230000035945 sensitivity Effects 0.000 description 1
- 238000002791 soaking Methods 0.000 description 1
- 238000003860 storage Methods 0.000 description 1
- 239000005720 sucrose Substances 0.000 description 1
- 238000004381 surface treatment Methods 0.000 description 1
- 229920001567 vinyl ester resin Polymers 0.000 description 1
- 239000000080 wetting agent Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L61/00—Compositions of condensation polymers of aldehydes or ketones; Compositions of derivatives of such polymers
- C08L61/20—Condensation polymers of aldehydes or ketones with only compounds containing hydrogen attached to nitrogen
- C08L61/26—Condensation polymers of aldehydes or ketones with only compounds containing hydrogen attached to nitrogen of aldehydes with heterocyclic compounds
- C08L61/28—Condensation polymers of aldehydes or ketones with only compounds containing hydrogen attached to nitrogen of aldehydes with heterocyclic compounds with melamine
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L61/00—Compositions of condensation polymers of aldehydes or ketones; Compositions of derivatives of such polymers
- C08L61/20—Condensation polymers of aldehydes or ketones with only compounds containing hydrogen attached to nitrogen
- C08L61/32—Modified amine-aldehyde condensates
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L2205/00—Polymer mixtures characterised by other features
- C08L2205/03—Polymer mixtures characterised by other features containing three or more polymers in a blend
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L33/00—Compositions of homopolymers or 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 of salts, anhydrides, esters, amides, imides or nitriles thereof; Compositions of derivatives of such polymers
- C08L33/02—Homopolymers or copolymers of acids; Metal or ammonium salts thereof
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/12—All metal or with adjacent metals
- Y10T428/12493—Composite; i.e., plural, adjacent, spatially distinct metal components [e.g., layers, joint, etc.]
- Y10T428/12535—Composite; i.e., plural, adjacent, spatially distinct metal components [e.g., layers, joint, etc.] with additional, spatially distinct nonmetal component
- Y10T428/12611—Oxide-containing component
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/25—Web or sheet containing structurally defined element or component and including a second component containing structurally defined particles
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/25—Web or sheet containing structurally defined element or component and including a second component containing structurally defined particles
- Y10T428/254—Polymeric or resinous material
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/31504—Composite [nonstructural laminate]
- Y10T428/31942—Of aldehyde or ketone condensation product
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/31504—Composite [nonstructural laminate]
- Y10T428/31942—Of aldehyde or ketone condensation product
- Y10T428/31946—Next to second aldehyde or ketone condensation product
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/31504—Composite [nonstructural laminate]
- Y10T428/31942—Of aldehyde or ketone condensation product
- Y10T428/31949—Next to cellulosic
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T442/00—Fabric [woven, knitted, or nonwoven textile or cloth, etc.]
- Y10T442/20—Coated or impregnated woven, knit, or nonwoven fabric which is not [a] associated with another preformed layer or fiber layer or, [b] with respect to woven and knit, characterized, respectively, by a particular or differential weave or knit, wherein the coating or impregnation is neither a foamed material nor a free metal or alloy layer
Definitions
- the present invention relates to melamine resin films and / or films made from cellulose-containing fibrous materials containing an aqueous solution
- the invention further relates to special aqueous synthetic resin mixtures.
- Thermoplastic films are usually used for 3D coating of materials, e.g. for coating wood-based materials in the furniture industry.
- the significant advantage of these thermoplastic films has so far been their elasticity, disadvantageous are the high costs in the manufacture, among other things. caused by the additional use of adhesives and the expected disposal costs.
- melamine resin films are mainly used for the surface treatment of wood-based materials such as chipboard, hardboard and blockboard.
- the melamine resin films are glued to the surfaces or edges of the wood-based materials with a suitable adhesive, if necessary using heat and pressure.
- the coating with melamine resin films is intended to improve the resistance of the wood-based materials to mechanical stresses and their water resistance.
- the melamine resins were modified, for example by adding guanamine according to DE-A 44 39 156 or by adding small amounts of an aqueous synthetic resin dispersion according to DE-A 38 37965.
- a combination of aminoplast resins with acrylate dispersions brings about a certain elasticity of the films produced according to DE-A 3700 344.
- the patents described above only disclose the production of so-called soft edges. When coating the soft edges with these melamine resin films, as described in the examples, adhesives are required in order to attach the resin films to the edges.
- the known melamine resin films can still be improved with regard to their deformability.
- the furniture manufacturers for the uniform coating of surfaces with three-dimensional structures such as those e.g. in some styles (country-style furniture) and / or moldings, it is desirable that melamine resin films or melamine resin films can be used which, compared to the known ones, have improved elasticity with improved or at least equally good other properties.
- the coating should be carried out in a single pressing process. The main characteristic of such foils or films lies in their deformability during the pressing process.
- the present invention was based on the object of identifying melamine resin films and / or films which are suitable for the flat coating of three-dimensionally structured surfaces, shaped bodies and three-dimensionally structured objects with sharp-edged elements and yet have the usual quality features of a melamine resin film or film. Furthermore, a synthetic resin mixture is to be made available which is particularly advantageous for impregnating cellulose-containing fibrous materials for the production of melamine resin films for 3D coating.
- the object was achieved by using melamine resin films and / or films made from cellulose-containing fibrous materials or fabrics containing an aqueous solution
- aqueous solutions for the subsequent or preliminary and subsequent soaking of the cellulose-containing fibrous materials are particularly suitable if they are
- Formaldehyde condensation product and (iii) 20 to 90% by weight, in particular 30 to 80% by weight, of a polymer dispersion
- Auxiliaries and additives can also be added to the melamine resin mixture according to the invention, for example 0.1 to 50% by weight, preferably 0.2 to 30% by weight, in particular 0.5 to 20% by weight of urea, caprolactam, Phenyl diglycol, butanediol and / or sucrose, based on 100% by weight of the mixture (i) to (iii). It can also contain conventional additives such as wetting agents, curing agents and catalysts.
- Melamine-formaldehyde condensation products are used as structural component (i).
- the production of the structural component (i) is generally known.
- melamine-formaldehyde condensation products are etherified with d- to C-alkanols such as methanol, ethanol, propanol and / or butanol. Methanol and ethanol are preferred.
- the production of the structural component (ii) is generally known.
- the melamine-formaldehyde condensation product is typically mixed with 20 to 30 mol of methanol and etherified at pH values from 1 to 5 and temperatures from 40 to 80 ° C.
- the condensation conditions depend on the water dilutability desired for the resin, which is at least 1: 6.
- the melamine resins are freed from excess alcohol and formaldehyde by distillation. Possibly present residual formaldehyde is the addition of urea at temperatures from room temperature to 90 ° C preferably reacted 60 to 70 C C.
- copolymer dispersions are used, the copolymers of which preferably contain carboxyl, hydroxyl, amide, glycidyl, carbonyl, N-methylol, N-alkoxymethyl, amino and / or hydrazo groups.
- the above-mentioned functional groups in the copolymer are obtained in a customary manner by polymerizing in corresponding monomers which carry these functional groups.
- the copolymers generally contain the abovementioned functional groups in such an amount that they can contain 0.1 to 50% by weight, preferably 0.3 to 20% by weight, based on the copolymer, of these monomers having functional groups in copolymerized form.
- the main monomers of the comonomers with the abovementioned groups are the customary, copolymerizable olefinically unsaturated monomers, for example C to C 2 alkyl esters of acrylic acid and methacrylic acid, preferably d to C 8 alkyl esters, for example methyl acrylate, methyl methacrylate, ethyl acrylate, ethyl methacrylate , Propyl acrylate, propyl methacrylate, butyl acrylate, butyl methacrylate, 2-ethylhexyl acrylate, 2-ethylhexyl methacrylate, lauryl acrylate and lauryl methacrylate; Vinyl esters of C 2 to C 4 carboxylic acids, for example vinyl acetate and vinyl propionate, C to C 4 dialkyl esters of maleic acid and fumaric acid, vinyl aromatics such as styrene, ⁇ -methylstyrene, vinyltolu
- the pH of the polymer dispersion is usually adjusted to 7.5 to 10 before the addition of the other components.
- the melamine resin film and / or film used according to the invention has the required high elasticity, which is necessary for coating three-dimensionally structured surfaces and / or moldings and / or structured objects with sharp-edged elements, without sacrificing the other quality properties.
- Sharp-edged elements are understood to mean, inter alia, edges, corners and tapering which describe a defined angle which results from two or more planes converging towards one another.
- cellulose-containing fibrous materials or fabrics or decorative paper are used in a manner known per se.
- the cellulose-containing fibrous materials are mixed with the melamine resin mixture (i) to (iii) according to the invention or with a melamine-formaldehyde impregnating resin or with a mixture of melamine-formaldehyde impregnating resins and lacquer resins or with a mixture of urea-formaldehyde resins and melamine resins.
- Pre-impregnated with urea-formaldehyde resins For every 100 parts by weight there are 25 to 85 parts by weight of the melamine resin mixture, based on the solids content of the melamine resin mixture.
- the impregnated fibrous materials are then dried to melamine resin films or melamine resin films in the customary manner, e.g. in a hot air stream at temperatures from 140 to 200 ° C.
- the further processing of the melamine resin films or melamine resin films is carried out by impregnating them with the melamine resin mixture (i) to (iii) and, if appropriate, using heat and pressure to bond the material part to be coated with the three-dimensionally structured surface.
- Preferred materials are wood-based materials, e.g. Country-style furniture and "Oriented Strand Board” (OSB) panels.
- the bonding is preferably carried out flat in a single work step, i.e. the three-dimensionally structured surface is coated with a single melamine resin film or sheet protruding over the complete structure in a single pressing process.
- the term “melamine resin film” is understood to mean a non-self-adhesive film, the term “melamine resin film” describing a self-adhesive film.
- Luhydran® S 937 T from BASF Aktiengesellschaft, a copolymer from an aqueous, hydroxyl-containing dispersion of a copolymer based on acrylic and methacrylic acid esters and styrene
- Decorative paper with a basis weight of 80 g / m 2 was pre-impregnated with component (i) (70% resin application based on the paper weight). After addition of 0.5% by weight hardener based on the synthetic resin mixture (eg hardener 529 liquid from BASF Aktiengesellschaft), the synthetic resin mixture from Example 1 was knife-coated onto the pre-impregnated decorative paper and then dried, so that the decorative papers had a solids content of 120 to 130% and had a residual moisture of 6 to 10%.
- hardener based on the synthetic resin mixture eg hardener 529 liquid from BASF Aktiengesellschaft
- Comparative example With the addition of 0.5% by weight of hardener based on component (i) (for example hardener 529 liquid from BASF Aktiengesellschaft), decorative paper with a weight of 80 g / m 2 was impregnated with and dried that the decorative papers had a solid content in the full impregnation of 120 to 130% and a residual moisture content of 6 to 10%.
- 3D coating and characterization With the addition of 0.5% by weight of hardener based on component (i) (for example hardener 529 liquid from BASF Aktiengesellschaft), decorative paper with a weight of 80 g / m 2 was impregnated with and dried that the decorative papers had a solid content in the full impregnation of 120 to 130% and a residual moisture content of 6 to 10%.
- the melamine resin film obtained was pressed onto an MDF (Medium Density Fiber) plate with a diameter of 16.5 cm including a 3D structure.
- 3D structures are contours with round and straight surfaces and / or edges with a defined angle.
- the pressing process took place in a laboratory press at 150 to 160 ° C under the force of 45 kN and in a time of 30-60 s.
- the deformability and the adhesion of the melamine resin film to the MDF board including a 3D structure was assessed.
- the coating should lie completely against the structure and adhere firmly to it without tearing or breaking.
- the resulting melamine resin film was placed on an MDF board at a temperature of 160-
- the quality of the hardening was determined by exposure to 0.2N hydrochloric acid for 16 hours
- the surface is not attacked by the acid.
- the strength of the attack can be judged from the strength of the red color.
- the closed or porous nature of the coated surface is used to assess the sensitivity to dirt.
- the surface to be tested was rubbed with black shoe polish and then cleaned again with a rag.
- the shoe polish remaining in the pores enables the closed surfaces to be assessed.
- Black degree The black degree was measured according to D 3265 with a tint tester 527 with brightness measuring head tint sensor. The measuring range covers 0-99.99 brightness units, whereby zero is the lowest brightness level (absolutely black). At values> 0.8, a distinct graying can already be seen. After the device was calibrated with a standard, the test specimen was measured three times and the mean value was given as black level.
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Abstract
The invention relates to the use of melamine resin foils and/or films for coating three-dimensionally structured surfaces and/or moulded bodies, made of fibrous material containing cellulose, which are post-impregnated or pre-impregnated and post-impregnated with an aqueous solution containing (i) a melamine formaldehyde condensate, (ii) an etherified melamine formaldehyde condensate and (iii) a polymer dispersion.
Description
Verwendung von Melaminharzfolien und/oder -filmen zur Beschichtung von dreidimensional strukturierten Oberflächen und/oder FormkörpernUse of melamine resin films and / or films for coating three-dimensionally structured surfaces and / or moldings
Beschreibungdescription
Die vorliegende Erfindung betrifft Melaminharzfolien und/oder -filme hergestellt aus cellulosehaltigen Faserstoffen, welche mit einer wässrigen Lösung enthaltendThe present invention relates to melamine resin films and / or films made from cellulose-containing fibrous materials containing an aqueous solution
(i) ein Melamin-Formaldehyd-Kondensat, (ii) ein verethertes Melamin-Formaldehyd-Kondensat und (iii) eine Polymer-Dispersion(i) a melamine-formaldehyde condensate, (ii) an etherified melamine-formaldehyde condensate and (iii) a polymer dispersion
nach- oder vor- und nachgetränkt wurden, zur Beschichtung von dreidimensional strukturierten Oberflächen und/oder Formkörpern (3D Beschichtung). Weiterhin betrifft die Erfindung spezielle wässrige Kunstharzmischungen.were impregnated or pre-impregnated, for the coating of three-dimensionally structured surfaces and / or moldings (3D coating). The invention further relates to special aqueous synthetic resin mixtures.
Üblicherweise werden zur 3D Beschichtung von Werkstoffen Thermoplastfolien verwendet, z.B. zum Beschichten von Holzwerkstoffen in der Möbelindustrie. Der bedeutende Vorteil dieser Thermoplastfolien ist bislang deren Elastizität, nachteilig sind die hohen Kosten in der Herstel- lung u.a. verursacht durch die zusätzliche Verwendung von Klebemitteln, und die zu erwartenden Kosten für die Entsorgung. Wünschenswert ist, die selbstklebenden kostengünstigen Mel- aminharzfilme, die z.B. in der Möbelindustrie zur Veredelung von glatten Oberflächen verwendet werden, ebenso zur Beschichtung von dreidimensional strukturierten Flächen einzusetzen. Reine Melaminharze sind für diese Anwendung zu spröde. Verbesserte Flexibilität konnte nach DE-A 23 09334 mit veretherten Methylolgruppen tragenden Melaminharzen erzielt werden. Diese werden hauptsächlich zur Herstellung von Verbundwerkstoffen wie Melaminharzfolien eingesetzt. Hierzu werden z.B. Papiere, Gewebe oder Vliese mit dem Melaminharz imprägniert und bei Temperaturen von 100 bis 180°C ausgehärtet. Diese Melaminharzfolien werden vor allem zur Oberflächenvergütung von Holzwerkstoffen wie Span-Hartfaser- und Tischlerplatten einge- setzt. Die Melaminharzfolien werden hierzu mit einem geeigneten Klebstoff, gegebenenfalls unter Anwendung von Hitze und Druck, auf die Flächen oder Kanten der Holzwerkstoffe geklebt. Durch die Beschichtung mit Melaminharzfolien soll die Widerstandsfähigkeit der Holzwerkstoffe gegenüber mechanischen Beanspruchungen und ihre Wasserfestigkeit verbessert werden.Thermoplastic films are usually used for 3D coating of materials, e.g. for coating wood-based materials in the furniture industry. The significant advantage of these thermoplastic films has so far been their elasticity, disadvantageous are the high costs in the manufacture, among other things. caused by the additional use of adhesives and the expected disposal costs. It is desirable that the self-adhesive, inexpensive melamine resin films, e.g. used in the furniture industry for finishing smooth surfaces, as well as for coating three-dimensionally structured surfaces. Pure melamine resins are too brittle for this application. According to DE-A 23 09334, improved flexibility could be achieved with etherified melamine resins bearing methylol groups. These are mainly used for the production of composite materials such as melamine resin films. For this, e.g. Papers, fabrics or nonwovens impregnated with the melamine resin and cured at temperatures from 100 to 180 ° C. These melamine resin films are mainly used for the surface treatment of wood-based materials such as chipboard, hardboard and blockboard. For this purpose, the melamine resin films are glued to the surfaces or edges of the wood-based materials with a suitable adhesive, if necessary using heat and pressure. The coating with melamine resin films is intended to improve the resistance of the wood-based materials to mechanical stresses and their water resistance.
Um die zur Beschichtung von beispielsweise abgerundeten Kanten erforderliche Flexibilität und Elastizität zu erreichen, wurden die Melaminharze modifiziert, z.B. durch Zugabe von Guanamin nach DE-A 44 39 156 oder durch Zugabe geringer Mengen an einer wässrigen Kunstharz- Dispersion nach DE-A 38 37965. Eine Kombination von Aminoplastharzen mit Acrylat- Dispersionen bewirkt nach DE-A 3700 344 eine gewisse Elastizität der hergestellten Folien. Die
oben beschriebenen Patentschriften offenbaren ausschließlich die Herstellung von sogenannten Softkanten. Beim Beschichten der Softkanten mit diesen Melaminharzfolien werden wie in den Beispielen beschrieben Kleber benötigt, um die Harzfolien auf die Kanten zu befestigen.In order to achieve the flexibility and elasticity required for coating rounded edges, for example, the melamine resins were modified, for example by adding guanamine according to DE-A 44 39 156 or by adding small amounts of an aqueous synthetic resin dispersion according to DE-A 38 37965. A combination of aminoplast resins with acrylate dispersions brings about a certain elasticity of the films produced according to DE-A 3700 344. The The patents described above only disclose the production of so-called soft edges. When coating the soft edges with these melamine resin films, as described in the examples, adhesives are required in order to attach the resin films to the edges.
Die bekannten Melaminharzfolien sind, was die Eigenschaft der Verformbarkeit betrifft, noch verbesserungsfähig. Insbesondere werden von den Möbelherstellern für die einheitliche Beschichtung von Flächen mit dreidimensionalen Strukturen, wie sie z.B. bei einigen Stilrichtungen (Möbel im Landhausstil) zu finden sind, und/oder von Formkörpern gewünscht, dass Melaminharzfolien oder Melaminharzfilme verwendet werden können, die gegenüber den bekannten eine verbesserte Elastizität aufweisen bei verbesserten oder mindestens gleich guten übrigen Eigenschaften. Darüber hinaus besteht der Wunsch, dreidimensionale Strukturen mit scharfkantigen Elementen flächig aus einem Material beschichten zu können. Bevorzugt sollen durch Modifizierung selbstklebende Melaminharzfilme, die bislang nur zur Beschichtung von glatten Oberflächen geeignet waren, zur 3D Beschichtung aufgezeigt werden. Die Beschichtung soll aus ästhe- tischen Gründen und gleichzeitig zur Vereinfachung der Herstellung in einem einzigen Presspro- zess erfolgen. Das Hauptmerkmal solcher Folien bzw. Filme liegt in der Verformbarkeit während des Pressprozesses.The known melamine resin films can still be improved with regard to their deformability. In particular, the furniture manufacturers for the uniform coating of surfaces with three-dimensional structures, such as those e.g. in some styles (country-style furniture) and / or moldings, it is desirable that melamine resin films or melamine resin films can be used which, compared to the known ones, have improved elasticity with improved or at least equally good other properties. There is also a desire to be able to coat three-dimensional structures with sharp-edged elements flat from one material. Modification is preferably used to show self-adhesive melamine resin films, which were previously only suitable for coating smooth surfaces, for 3D coating. For aesthetic reasons and at the same time to simplify production, the coating should be carried out in a single pressing process. The main characteristic of such foils or films lies in their deformability during the pressing process.
Der vorliegenden Erfindung lag die Aufgabe zugrunde, Melaminharzfolien und/oder -filme auf- zuzeigen, die sich zur flächigen Beschichtung von dreidimensional strukturierten Oberflächen, Formkörpern und dreidimensional strukturierter Gegenstände mit scharfkantigen Elementen eignen und dennoch die üblichen Qualitätsmerkmale einer Melaminharzfolie oder -film aufweisen. Weiterhin soll eine Kunstharzmischung zur Verfügung gestellt werden, die sich besonders vorteilhaft zum Tränken von cellulosehaltigen Faserstoffen zur Herstellung von Melaminharzfil- men zur 3D Beschichtung eignet.The present invention was based on the object of identifying melamine resin films and / or films which are suitable for the flat coating of three-dimensionally structured surfaces, shaped bodies and three-dimensionally structured objects with sharp-edged elements and yet have the usual quality features of a melamine resin film or film. Furthermore, a synthetic resin mixture is to be made available which is particularly advantageous for impregnating cellulose-containing fibrous materials for the production of melamine resin films for 3D coating.
Gelöst wurde die Aufgabe durch die Verwendung von Melaminharzfolien und/oder filmen hergestellt aus cellulosehaltigen Faserstoffe oder Gewebe, die mit einer wässrigen Lösung enthaltendThe object was achieved by using melamine resin films and / or films made from cellulose-containing fibrous materials or fabrics containing an aqueous solution
(i) ein Melamin-Formaldehyd-Kondensat,(i) a melamine-formaldehyde condensate,
(ii) ein verethertes Melamin-Formaldehyd-Kondensat und(ii) an etherified melamine formaldehyde condensate and
(iii) eine Polymer-Dispersion(iii) a polymer dispersion
nach- oder vor- und nachgetränkt sind, zur Beschichtung von dreidimensional strukturierten Oberflächen und/oder Formkörpern (3D Beschichtung).
Es wurde gefunden, dass wässrige Lösungen zum Nach- oder Vor- und Nachtränken der cellulosehaltigen Faserstoffe besonders geeignet sind, wenn sieare impregnated or pre-impregnated, for the coating of three-dimensionally structured surfaces and / or moldings (3D coating). It has been found that aqueous solutions for the subsequent or preliminary and subsequent soaking of the cellulose-containing fibrous materials are particularly suitable if they are
(i) 5 bis 50 Gew.-%, insbesondere 10 bis 30 Gew.-% eines Melamin-Formaldehyd- Kondensationsproduktes,(i) 5 to 50% by weight, in particular 10 to 30% by weight, of a melamine-formaldehyde condensation product,
(ii) 5 bis 50 Gew.-%, insbesondere 10 bis 40 Gew.-% eines veretherten Melamin-(ii) 5 to 50% by weight, in particular 10 to 40% by weight, of an etherified melamine
Formaldehyd-Kondensationsproduktes, und (iii) 20 bis 90 Gew.-%, insbesondere 30 bis 80 Gew.-% einer Polymer-DispersionFormaldehyde condensation product, and (iii) 20 to 90% by weight, in particular 30 to 80% by weight, of a polymer dispersion
enthalten. Die Mengenangaben der Komponenten (i), (ii) und (iii) ergänzen sich auf 100 Gew.-% und beziehen sich auf die Flüssigharzmischung.contain. The amounts of components (i), (ii) and (iii) add up to 100% by weight and relate to the liquid resin mixture.
Der erfindungsgemäßen Melaminharz-Mischung können noch Hilfs- und Zusatzmittel zugesetzt werden, beispielsweise 0,1 bis 50 Gew.-%, bevorzugt 0,2 bis 30 Gew.-%, insbesondere 0,5 bis 20 Gew.-% Harnstoff, Caprolactam, Phenyldiglykol, Butandiol und/oder Saccarose, bezogen auf 100 Gew.-% der Mischung (i) bis (iii). Des weiteren kann sie übliche Additive enthalten wie beispielsweise Netzmittel, Härtungsmittel und Katalysatoren.Auxiliaries and additives can also be added to the melamine resin mixture according to the invention, for example 0.1 to 50% by weight, preferably 0.2 to 30% by weight, in particular 0.5 to 20% by weight of urea, caprolactam, Phenyl diglycol, butanediol and / or sucrose, based on 100% by weight of the mixture (i) to (iii). It can also contain conventional additives such as wetting agents, curing agents and catalysts.
Es wurden ferner neue Kunstharzmischungen gefunden, die sich besonders vorteilhaft zur Her- Stellung von Melaminharzfilmen und -folien zur 3D Beschichtung eignen. Diese weisen folgende Zusammensetzung auf:Furthermore, new synthetic resin mixtures have been found which are particularly advantageous for the production of melamine resin films and foils for 3D coating. These have the following composition:
(i) 5 bis 50 Gew.-%, insbesondere 10 bis 20 Gew.-% eines Melamin-Formaldehyd- Kondensationsproduktes, (ii) 5 bis 50 Gew.-%, insbesondere 10 bis 30 Gew.-% eines veretherten Melamin- Formaldehyd-Kondensationsproduktes, und (iii) 40 bis 90 Gew.-%, insbesondere 50 bis 80 Gew.-% eines in Form einer wässrigen Dispersion vorliegenden und durch Kondensationsreaktion vernetzbaren Copolymerisates aus bevorzugt Carboxyl-, Hydroxy-, Amid-, Glycidyl-, Carbonyl-, N-Methylol, N-Alkoxy- methyl, Amino- und/oder Hydrazogruppen enthaltenden Acrylaten.(i) 5 to 50% by weight, in particular 10 to 20% by weight of a melamine-formaldehyde condensation product, (ii) 5 to 50% by weight, in particular 10 to 30% by weight of an etherified melamine-formaldehyde -Condensation product, and (iii) 40 to 90% by weight, in particular 50 to 80% by weight, of a copolymer which is present in the form of an aqueous dispersion and can be crosslinked by means of a condensation reaction and is preferably composed of carboxyl, hydroxyl, amide, glycidyl, carbonyl -, N-Methylol, N-alkoxy-methyl, amino and / or hydrazo groups containing acrylates.
Die Mengenangaben der Komponenten (i), (ii) und (iii) ergänzen sich auf 100 Gew.-% und beziehen sich auf die Flüssigharzmischung.The amounts of components (i), (ii) and (iii) add up to 100% by weight and relate to the liquid resin mixture.
Zu den Aufbaukomponenten ist im einzelnen folgendes auszuführen:The following must be carried out in detail for the structural components:
Als Aufbaukomponente (i) werden Melamin-Formaldehyd-Kondensationsprodukte verwendet. Die Herstellung der Aufbaukomponente (i) ist allgemein bekannt. In der Regel wird zunächst 1
Mol Melamin mit 1,4 bis 2 Mol Formaldehyd bei pH-Werten von 7 bis 9 und bei Temperaturen von 40 bis 100°C kondensiert, bis die geeignete Kondensationsgrad erreicht wird.Melamine-formaldehyde condensation products are used as structural component (i). The production of the structural component (i) is generally known. As a rule, 1 Mol of melamine condensed with 1.4 to 2 mol of formaldehyde at pH values from 7 to 9 and at temperatures from 40 to 100 ° C until the appropriate degree of condensation is reached.
In der Aufbaukomponente (ii) werden Melamin-Formaldehyd-Kondensationsprodukte mit d- bis C Alkanolen wie Methanol, Ethanol, Propanol und/oder Butanol verethert. Bevorzugt sind Methanol und Ethanol. Die Herstellung der Aufbaukomponente (ii) ist allgemein bekannt. Das Mel- amin-Formaldehyd-Kondensationsprodukt wird typischerweise mit 20 bis 30 Mol Methanol versetzt und bei pH-Werten von 1 bis 5 und Temperaturen von 40 bis 80°C verethert. Die Kondensationsbedingungen richten sich nach der für das Harz gewünschten Wasserverdünnbarkeit, die mindestens 1 :6 beträgt. Nach der Kondensation werden die Melaminharze durch Destillation von überschüssigem Alkohol und Formaldehyd befreit. Eventuell vorhandener restlicher Formaldehyd wird bei Zusatz von Harnstoff bei Temperaturen von Raumtemperatur bis 90°C, bevorzugt 60 bis 70CC umgesetzt.In the structural component (ii), melamine-formaldehyde condensation products are etherified with d- to C-alkanols such as methanol, ethanol, propanol and / or butanol. Methanol and ethanol are preferred. The production of the structural component (ii) is generally known. The melamine-formaldehyde condensation product is typically mixed with 20 to 30 mol of methanol and etherified at pH values from 1 to 5 and temperatures from 40 to 80 ° C. The condensation conditions depend on the water dilutability desired for the resin, which is at least 1: 6. After the condensation, the melamine resins are freed from excess alcohol and formaldehyde by distillation. Possibly present residual formaldehyde is the addition of urea at temperatures from room temperature to 90 ° C preferably reacted 60 to 70 C C.
Als Aufbaukomponente (iii) werden Copolymerisat-Dispersionen verwendet, deren Copolymeri- sate bevorzugt Carboxyl-, Hydroxy-, Amid-, Glycidyl-, Carbonyl-, N-Methylol, N-Alkoxymethyl, Amino- und/oder Hydrazogruppen enthalten. Die obengenannten funktioneilen Gruppen im Co- polymerisat werden auf übliche Weise durch Einpolymerisieren entsprechender Monomere, die diese funktionellen Gruppen tragen, erhalten.As the build-up component (iii), copolymer dispersions are used, the copolymers of which preferably contain carboxyl, hydroxyl, amide, glycidyl, carbonyl, N-methylol, N-alkoxymethyl, amino and / or hydrazo groups. The above-mentioned functional groups in the copolymer are obtained in a customary manner by polymerizing in corresponding monomers which carry these functional groups.
Die Copolymerisate enthalten die obengenannten funktioneilen Gruppen im allgemeinen in solchen Menge, dass sie 0,1 bis 50 Gew.-%, vorzugsweise 0,3 bis 20 Gew.-%, bezogen auf das Copolymerisat, dieser Monomeren mit funktioneilen Gruppen einpolymerisiert enthalten können.The copolymers generally contain the abovementioned functional groups in such an amount that they can contain 0.1 to 50% by weight, preferably 0.3 to 20% by weight, based on the copolymer, of these monomers having functional groups in copolymerized form.
Als Hauptmonomere der Comonomeren mit den obengenannten Gruppen eignen sich die üblichen, damit copolymerisierbaren olefinisch ungesättigten Monomeren, z.B. C bis Cι2-Alkylester der Acrylsäure und Methacrylsäure, bevorzugt d- bis C8-Alkylester, z.B. Methylacrylat, Methyl- methacrylat, Ethylacrylat, Ethylmethacrylat, Propylacrylat, Propylmethacrylat, Butylacrylat, Bu- tylmethacrylat, 2-Ethylhexylacrylat, 2-Ethylhexylmethacrylat, Laurylacrylat und Laurylmethacrylat; Vinylester von C2- bis C4-Carbonsäuren, z.B. Vinylacetat und Vinylpropionat, C bis C4-Dialkyl- ester der Maleinsäure und Fumarsäure, Vinylaromaten wie Styrol, α-Methylstyrol, Vinyltoluol; Acrylnitril, Methacrylnitril, Acrylamid, Methacrylamid sowie Vinylether mit 3 bis 10 Kohlenstoffatomen, Vinylhalogenide wie Vinylchlorid und Vinylidenchlorid; mehrfach olefinisch ungesättigte Verbindungen wie Butadien und Isopren sowie Gemische der obengenannten Monomeren, so- weit sie miteinander copolymerisierbar sind.The main monomers of the comonomers with the abovementioned groups are the customary, copolymerizable olefinically unsaturated monomers, for example C to C 2 alkyl esters of acrylic acid and methacrylic acid, preferably d to C 8 alkyl esters, for example methyl acrylate, methyl methacrylate, ethyl acrylate, ethyl methacrylate , Propyl acrylate, propyl methacrylate, butyl acrylate, butyl methacrylate, 2-ethylhexyl acrylate, 2-ethylhexyl methacrylate, lauryl acrylate and lauryl methacrylate; Vinyl esters of C 2 to C 4 carboxylic acids, for example vinyl acetate and vinyl propionate, C to C 4 dialkyl esters of maleic acid and fumaric acid, vinyl aromatics such as styrene, α-methylstyrene, vinyltoluene; Acrylonitrile, methacrylonitrile, acrylamide, methacrylamide and vinyl ethers having 3 to 10 carbon atoms, vinyl halides such as vinyl chloride and vinylidene chloride; polyolefinically unsaturated compounds such as butadiene and isoprene and mixtures of the above-mentioned monomers insofar as they are copolymerizable with one another.
Zur Herstellung der Kunstharzmischung wird üblicherweise der pH-Wert der Polymer-Dispersion vor der Zugabe der anderen Komponenten auf 7,5 bis 10 eingestellt.
Die erfindungsgemäß verwendeten Melaminharzfolie und/oder -film weist ohne Einbuße der übrigen Qualitätseigenschaften die erforderliche große Elastizität auf, die zur Beschichtung von dreidimensional strukturierter Oberflächen und/oder Formkörper und/oder strukturierten Ge- genständen mit scharfkantigen Elementen von Nöten ist. Unter scharfkantigen Elementen werden u.a. Kanten, Ecken und Zuspitzungen verstanden, die einen definierten Winkel beschreiben, der sich aus zwei oder mehreren aufeinander zulaufenden Ebenen ergibt.To produce the synthetic resin mixture, the pH of the polymer dispersion is usually adjusted to 7.5 to 10 before the addition of the other components. The melamine resin film and / or film used according to the invention has the required high elasticity, which is necessary for coating three-dimensionally structured surfaces and / or moldings and / or structured objects with sharp-edged elements, without sacrificing the other quality properties. Sharp-edged elements are understood to mean, inter alia, edges, corners and tapering which describe a defined angle which results from two or more planes converging towards one another.
Zur Herstellung der erfindungsgemäß zu verwendenden Melaminharzfolien oder -filme werden in an sich bekannter Weise saugfähige cellulosehaltige Faserstoffe oder Gewebe oder Dekor- papier verwendet.In order to produce the melamine resin films or films to be used according to the invention, cellulose-containing fibrous materials or fabrics or decorative paper are used in a manner known per se.
Die cellulosehaltigen Faserstoffe werden mit der erfindungsgemäßen Melaminharz-Mischung (i) bis (iii) oder mit einem Melamin-Formaldehyd-Tränkharz oder mit einer Mischung aus Melamin- Formaldehyd-Tränkharzen und Lackharzen oder mit einer Mischung aus Harnstoff-Formaldehyd-Harzen und Melamin-Harnstoff-Formaldehyd-Harzen vorgetränkt. Auf 100 Gewichtsteile kommen 25 bis 85 Gewichtsteile Melaminharz-Mischung, bezogen auf den Feststoffgehalt der Melaminharz-Mischung. Die Trocknung der imprägnierten Faserstoffe zu Melaminharzfolien bzw. Melaminharzfilmen erfolgt anschließend in üblicher Weise, z.B. im Heißluftstrom bei Tem- peraturen von 140 bis 200°C. Die Weiterverarbeitung der Melaminharzfolien bzw. Melaminharzfilme erfolgt in dem man sie mit der Melaminharz-Mischung (i) bis (iii) nachtränkt und gegebenenfalls unter Anwendung von Hitze und Druck auf das zu beschichtende Werkstoffteil mit der dreidimensional strukturierten Oberfläche klebt. Bevorzugte Werkstoffe sind Holzwerkstoffe, z.B. Möbel im Landhausstil, und "Oriented Strand Board" (OSB) Platten. Die Verklebung erfolgt vor- zugsweise flächig in einem einzigen Arbeitsschritt, d.h. die dreidimensional strukturierte Oberfläche wird mit einem einzigen über die komplette Struktur ragenden Melaminharzfilm oder -folie in einem einzigen Pressvorgang beschichtet.The cellulose-containing fibrous materials are mixed with the melamine resin mixture (i) to (iii) according to the invention or with a melamine-formaldehyde impregnating resin or with a mixture of melamine-formaldehyde impregnating resins and lacquer resins or with a mixture of urea-formaldehyde resins and melamine resins. Pre-impregnated with urea-formaldehyde resins. For every 100 parts by weight there are 25 to 85 parts by weight of the melamine resin mixture, based on the solids content of the melamine resin mixture. The impregnated fibrous materials are then dried to melamine resin films or melamine resin films in the customary manner, e.g. in a hot air stream at temperatures from 140 to 200 ° C. The further processing of the melamine resin films or melamine resin films is carried out by impregnating them with the melamine resin mixture (i) to (iii) and, if appropriate, using heat and pressure to bond the material part to be coated with the three-dimensionally structured surface. Preferred materials are wood-based materials, e.g. Country-style furniture and "Oriented Strand Board" (OSB) panels. The bonding is preferably carried out flat in a single work step, i.e. the three-dimensionally structured surface is coated with a single melamine resin film or sheet protruding over the complete structure in a single pressing process.
Unter dem Begriff "Melaminharzfolie" ist im Rahmen dieser Erfindung eine nicht selbstklebende Folie zu verstehen, wobei der Begriff "Melaminharzfilm" einen selbstklebenden Film beschreibt.In the context of this invention, the term “melamine resin film” is understood to mean a non-self-adhesive film, the term “melamine resin film” describing a self-adhesive film.
Die erhaltenden Oberflächen sind klar und gut geschlossen bei guten Verformbarkeiten.The surfaces obtained are clear and well closed with good ductility.
Die Vorteile der Erfindung liegen auch in der Vermeidung von Kosten für die aufwendige Herstellung und Entsorgung der bislang verwendeten Thermoplastfolien.
BeispieleThe advantages of the invention also lie in the avoidance of costs for the complex production and disposal of the previously used thermoplastic films. Examples
Komponente (i): Melamin-Formaldehyd-KondensationsproduktComponent (i): melamine-formaldehyde condensation product
Kauramin-Tränkharz 753 der Firma BASF Aktiengesellschaft, enthaltend eine wässrige Lösung eines modifizierten Melamin-Formaldehyd-Kondensationsproduktes (Modifizierungsmittel: Butandiol)Kauramine impregnating resin 753 from BASF Aktiengesellschaft, containing an aqueous solution of a modified melamine-formaldehyde condensation product (modifier: butanediol)
Komponente (ii): verethertes Melamin-Formaldehyd-Kondensationsprodukt 126 g Melamin wurde in Gegenwart von 270 g Formaldehyd bei einem pH-Wert von 8,5 und Temperaturen von 40 bis 70°C methyloliert. Die erhaltene Additionsverbindung wurde mit Ameisensäure auf einen pH-Wert von 4 eingestellt und bei Temperaturen von 60°C mit 900 g Methanol während einer Dauer von 15 min. verethert. Nach Neutralisation mit Natronlauge wurde die Reaktionslösung durch Einengen (Destillation) von dem nichtumgesetzten Formaldehyd sowie dem überschüssigen Methanol befreit.Component (ii): etherified melamine-formaldehyde condensation product 126 g of melamine was methylolated in the presence of 270 g of formaldehyde at a pH of 8.5 and temperatures of 40 to 70 ° C. The addition compound obtained was adjusted to a pH of 4 with formic acid and at temperatures of 60 ° C. with 900 g of methanol for a period of 15 min. etherified. After neutralization with sodium hydroxide solution, the unreacted formaldehyde and the excess methanol were freed from the reaction solution by concentration (distillation).
Komponente (iii): Polymer-DispersionComponent (iii): polymer dispersion
Luhydran® S 937 T der Firma BASF Aktiengesellschaft, ein Copolymerisat aus einer wässrigen, hydroxylgruppenhaltigen Dispersion eines Copolymers auf der Basis von Acryl- und Methacryl- säureestern sowie StyrolLuhydran® S 937 T from BASF Aktiengesellschaft, a copolymer from an aqueous, hydroxyl-containing dispersion of a copolymer based on acrylic and methacrylic acid esters and styrene
Beispiel 1example 1
20 g der Komponente (i), 30 g der Komponente (ii) und 40 g der Komponente (iii) wurden bei einem pH-Wert 7 bis 9 bei Temperatur von 20 bis 30°C gemischt. Die erhaltene Kunstharz- Mischung war mindestens 24 Stunden lagerstabil.20 g of component (i), 30 g of component (ii) and 40 g of component (iii) were mixed at pH 7 to 9 at a temperature of 20 to 30 ° C. The synthetic resin mixture obtained was stable in storage for at least 24 hours.
Anwendungsbeispiel:Example of use:
Dekorpapier mit einem Flächengewicht von 80 g/m2 wurde mit der Komponente (i) vorimprägniert (70 % Harzauftrag bezogen auf das Papiergewicht). Die Kunstharzmischung aus dem Beispiel 1 wurde nach Zusatz von 0,5 Gew.-% Härter bezogen auf die Kunstharzmischung (z.B. Härter 529 Flüssig der Firma BASF Aktiengesellschaft) auf das vorimprägnierte Dekorpapier aufgerakelt und anschließend getrocknet, so dass die Dekorpapiere einen Feststoffgehalt von 120 bis 130 % aufwiesen und eine Restfeuchtigkeit von 6 bis 10 % besaßen.Decorative paper with a basis weight of 80 g / m 2 was pre-impregnated with component (i) (70% resin application based on the paper weight). After addition of 0.5% by weight hardener based on the synthetic resin mixture (eg hardener 529 liquid from BASF Aktiengesellschaft), the synthetic resin mixture from Example 1 was knife-coated onto the pre-impregnated decorative paper and then dried, so that the decorative papers had a solids content of 120 to 130% and had a residual moisture of 6 to 10%.
Vergleichsbeispiel: Mit der Komponente (i) wurde nach Zusatz von 0,5 Gew.-% Härter bezogen auf die Komponente (i) (z.B. Härter 529 Flüssig der Firma BASF Aktiengesellschaft) Dekorpapier mit einem Gewicht von 80 g/m2 so imprägniert und getrocknet, dass die Dekorpapiere einen Feststoffgehalt in der Volltränkung von 120 bis 130 % aufwiesen und eine Restfeuchtigkeit von 6 bis 10 % besaßen.
3D-Beschichtung und Charakterisierung:Comparative example: With the addition of 0.5% by weight of hardener based on component (i) (for example hardener 529 liquid from BASF Aktiengesellschaft), decorative paper with a weight of 80 g / m 2 was impregnated with and dried that the decorative papers had a solid content in the full impregnation of 120 to 130% and a residual moisture content of 6 to 10%. 3D coating and characterization:
Der erhaltene Melaminharzfilm wurde auf eine MDF (Medium Density Fiber) Platte mit einem Durchmesser von 16,5 cm beinhaltend eine 3D Struktur gepresst. Unter 3D Strukturen sind Konturen mit runden und geraden Flächen und/oder Kanten mit definiertem Winkel zu verstehen. Der Pressvorgang fand in einer Laborpresse bei 150 bis 160°C unter einer Krafteinwirkung von 45 kN und in einer Zeit von 30-60 s statt.The melamine resin film obtained was pressed onto an MDF (Medium Density Fiber) plate with a diameter of 16.5 cm including a 3D structure. 3D structures are contours with round and straight surfaces and / or edges with a defined angle. The pressing process took place in a laboratory press at 150 to 160 ° C under the force of 45 kN and in a time of 30-60 s.
Die Verformbarkeit und die Haftung des Melaminharzfilms auf der MDF Platte beinhaltend eine 3D Struktur wurde beurteilt. Bei guter Verformbarkeit soll die Beschichtung vollständig an der Struktur anliegen und fest an dieser haften ohne zu reißen oder zu brechen.The deformability and the adhesion of the melamine resin film to the MDF board including a 3D structure was assessed. In the case of good deformability, the coating should lie completely against the structure and adhere firmly to it without tearing or breaking.
Charakterisierung der Oberfläche:Characterization of the surface:
Der erhaltende Melaminharzfilm wurde auf eine MDF Platte bei einer Temperatur von 160-The resulting melamine resin film was placed on an MDF board at a temperature of 160-
165°C unter einem Druck von 25 Kp und in einer Zeit von 110 s gepresst. Folgenden Prüfungen wurden durchgeführt:165 ° C under a pressure of 25 Kp and pressed in a time of 110 s. The following tests were carried out:
Härtung:cure:
Die Güte der Härtung wurde durch 16-stündige Einwirkung einer 0,2 n Salzsäure, die mitThe quality of the hardening was determined by exposure to 0.2N hydrochloric acid for 16 hours
0,004 Gew.-% Rhodamin B-Lösung angefärbt ist, auf die beschichtete MDF-Platte ermittelt.0.004% by weight of rhodamine B solution is stained, determined on the coated MDF board.
Bei guter Härtung wird die Oberfläche nicht durch die Säure angegriffen. Die Stärke des Angriffs lässt sich anhand der Stärke der Rotfärbung beurteilen.With good hardening, the surface is not attacked by the acid. The strength of the attack can be judged from the strength of the red color.
Beurteilung:Evaluation:
0 = kein Angriff0 = no attack
1 = schwache Rosafärbung1 = weak pink color
2 = deutliche Rotfärbung 3 = starke Rotfärbung2 = clear red color 3 = strong red color
4 = starke Rotfärbung mit leichter Oberflächenquellung4 = strong red color with slight surface swelling
5 = starke Rotfärbung mit starker Oberflächenquellung5 = strong red color with strong surface swelling
6 = zerstörte Oberfläche6 = destroyed surface
Geschlossenheit:Unity:
Die Geschlossenheit oder Porigkeit der beschichteten Oberfläche dient zur Beurteilung der Schmutzempfindlichkeit. Die zu prüfende Oberfläche wurde mit schwarzer Schuhcreme eingerieben und anschließend mit einem Lappen wieder gereinigt. Die in den Poren verbleibende Schuhcreme ermöglicht eine Beurteilung der Geschlossenheit der Oberflächen. Die Beurteilung der Oberflächengeschlossenheit erfolgt in folgenden Stufen:
0 = porenfreiThe closed or porous nature of the coated surface is used to assess the sensitivity to dirt. The surface to be tested was rubbed with black shoe polish and then cleaned again with a rag. The shoe polish remaining in the pores enables the closed surfaces to be assessed. The surface closeness is assessed in the following stages: 0 = non-porous
1 = vereinzelte Poren1 = isolated pores
2 = wenige Poren2 = few pores
3 = häufige Poren3 = frequent pores
4 = viele offene Stellen4 = many vacancies
5 = sehr viele offene Stellen5 = many vacancies
6 = keine Geschlossenheit.6 = no unity.
Schwarzgrad: Die Schwarzgradmessung erfolgte nach D 3265 mit einem Tint Tester 527 mit Helligkeitsmesskopf Tint Sensor. Der Messbereich umfasst 0-99,99 Helligkeitseinheiten, wobei Null als niedrigste Helligkeitsstufe (absolut schwarz) gilt. Bei Werten >0,8 ist bereits eine deutliche Vergrauung erkennbar. Nach Eichung des Gerätes mit einem Standard wurde der Prüfkörper dreimal vermessen und der Mittelwert als Schwarzgrad angegeben.Black degree: The black degree was measured according to D 3265 with a tint tester 527 with brightness measuring head tint sensor. The measuring range covers 0-99.99 brightness units, whereby zero is the lowest brightness level (absolutely black). At values> 0.8, a distinct graying can already be seen. After the device was calibrated with a standard, the test specimen was measured three times and the mean value was given as black level.
Die Resultate sind in der Tabelle 1 präsentiert.The results are presented in Table 1.
Tabelle 1:Table 1:
Claims
1. Verwendung von Melaminharzfolien und/oder -filmen hergestellt aus cellulosehaltigen Faserstoffen, welche mit einer wässrigen Lösung enthaltend1. Use of melamine resin films and / or films made from cellulose-containing fibrous materials containing an aqueous solution
(i) ein Melamin-Formaldehyd-Kondensat,(i) a melamine-formaldehyde condensate,
(ii) ein verethertes Melamin-Formaldehyd-Kondensat und(ii) an etherified melamine formaldehyde condensate and
(iii) eine Polymer-Dispersion(iii) a polymer dispersion
nach- oder vor- und nachgetränkt werden, zur Beschichtung von dreidimensional strukturierten Oberflächen und/oder Formkörpern (3D Beschichtung).be impregnated or pre-impregnated, for the coating of three-dimensionally structured surfaces and / or moldings (3D coating).
2. Verwendung nach Anspruch 1 , wobei die wässrige Lösung2. Use according to claim 1, wherein the aqueous solution
(i) 5 bis 50 Gew.-% eines Melamin-Formaldehyd-Kondensationsproduktes,(i) 5 to 50% by weight of a melamine-formaldehyde condensation product,
(ii) 5 bis 50 Gew.-% eines verethertes Melamin-Formaldehyd-Kondensats und (iii) 20 bis 70 Gew.-% einer Polymer-Dispersion(ii) 5 to 50% by weight of an etherified melamine-formaldehyde condensate and (iii) 20 to 70% by weight of a polymer dispersion
enthält, wobei sich die Mengenangaben der Komponenten (i), (ii) und (iii) auf 100 Gew.-% ergänzen und sich auf die Flüssigharzmischung beziehen.contains, the amounts of components (i), (ii) and (iii) add up to 100% by weight and relate to the liquid resin mixture.
3. Verwendung nach den Ansprüchen 1 und 2, wobei die Dispersion (iii) Copolymerisate aus Carboxyl-, Hydroxy-, Amid-, Glycidyl-, Carbonyl-, N-Methylol, N-Alkoxymethyl, Amino- und/oder Hydrazogruppen enthaltenden Acrylaten enthält.3. Use according to claims 1 and 2, wherein the dispersion (iii) contains copolymers of carboxyl, hydroxy, amide, glycidyl, carbonyl, N-methylol, N-alkoxymethyl, amino and / or hydrazo groups containing acrylates ,
4. Verwendung nach den Ansprüchen 1 bis 3, wobei die wässrige Lösung außerdem 0,1 bis 50 Gew.% Harnstoff, bezogen auf 100 Gew.-% der Mischung (i) bis (iii) enthält.4. Use according to claims 1 to 3, wherein the aqueous solution also contains 0.1 to 50% by weight of urea, based on 100% by weight of the mixture (i) to (iii).
5. Verwendung nach den Ansprüchen 1 bis 3, wobei die wässrige Lösung5. Use according to claims 1 to 3, wherein the aqueous solution
(i) 10 bis 30 Gew.-% eines Melamin-Formaldehyd-Kondensationsproduktes,(i) 10 to 30% by weight of a melamine-formaldehyde condensation product,
(ii) 10 bis 40 Gew.-% eines veretherten Melamin-Formaldehyd-Kondensationsproduk- tes, und (iii) 30 bis 80 Gew.-% einer Polymer-Dispersion(ii) 10 to 40% by weight of an etherified melamine-formaldehyde condensation product, and (iii) 30 to 80% by weight of a polymer dispersion
enthält, wobei sich die Mengenangaben der Komponenten (i), (ii) und (iii) auf 100 Gew.-% ergänzen und sich auf die Flüssigharzmischung beziehen. contains, the amounts of components (i), (ii) and (iii) add up to 100% by weight and relate to the liquid resin mixture.
6. Verwendung nach den Ansprüchen 1 bis 5 zur Beschichtung von Gegenständen mit SD- Oberflächen und/oder scharfkantigen Elementen.6. Use according to claims 1 to 5 for coating objects with SD surfaces and / or sharp-edged elements.
7. Verwendung nach den Ansprüchen 1 bis 5 zur Beschichtung mit einer einzigen Melamin- harzfolie und/oder -film.7. Use according to claims 1 to 5 for coating with a single melamine resin film and / or film.
8. Verwendung nach den Ansprüchen 1 bis 5 zur Beschichtung von Holzwerkstoffen.8. Use according to claims 1 to 5 for coating wood-based materials.
9. Verwendung nach den Ansprüchen 1 bis 5 zur Beschichtung von OSB Platten.9. Use according to claims 1 to 5 for coating OSB panels.
10. Verwendung nach Anspruch 1, wobei die cellulosehaltigen Faserstoffe mit Melamin- Formaldehyd-Tränkharzen oder einer Mischung aus Melamin-Formaldehyd-Tränkharzen und Lackharzen oder einer Mischung aus Harnstoff-Formaldehyd-Harzen und Melamin- Harnstoff-Formaldehyd-Harzen vorgetränkt werden und mit der wässrigen Lösung (i) bis (iii) gemäß Anspruch 1 nachgetränkt werden.10. Use according to claim 1, wherein the cellulose-containing fibrous materials are pre-impregnated with melamine-formaldehyde impregnating resins or a mixture of melamine-formaldehyde impregnating resins and coating resins or a mixture of urea-formaldehyde resins and melamine-urea-formaldehyde resins and with the aqueous solution (i) to (iii) according to claim 1.
11. Kunstharzmischung zum Tränken von cellulosehaltigen Faserstoffen, enthaltend11. Containing synthetic resin mixture for impregnating cellulose-containing fibrous materials
(i) 5 bis 50 Gew.-% eines Melamin-Formaldehyd-Kondensationsproduktes, (ii) 5 bis 50 Gew.-% eines veretherten Melamin-Formaldehyd-Kondensationsproduktes, und (iii) 40 bis 90 Gew.-% eines in Form einer wässrigen Dispersion vorliegenden und durch Kondensationsreaktion vernetzbaren Copolymerisates,(i) 5 to 50% by weight of a melamine-formaldehyde condensation product, (ii) 5 to 50% by weight of an etherified melamine-formaldehyde condensation product, and (iii) 40 to 90% by weight of one in the form of a aqueous dispersion and crosslinkable copolymer by condensation reaction,
wobei sich die Mengenangaben der Komponenten (i), (ii) und (iii) auf 100 Gew.-% ergänzen und sich auf die Flüssigharzmischung beziehen.where the amounts of components (i), (ii) and (iii) add up to 100% by weight and relate to the liquid resin mixture.
12. Kunstharzmischung nach Anspruch 11, wobei als Komponente (iii) ein Copolymerisat aus Carboxyl-, Hydroxy-, Amid-, Glycidyl-, Carbonyl-, N-Methylol, N-Alkoxymethyl, Amino- und/oder Hydrazogruppen enthaltenden Acrylaten verwendet wird.12. A synthetic resin mixture according to claim 11, wherein a copolymer of carboxyl, hydroxy, amide, glycidyl, carbonyl, N-methylol, N-alkoxymethyl, amino and / or hydrazo groups is used as component (iii).
13. Melaminharzfolien oder -filme, die mit der Kunstharzmischung gemäß den Ansprüchen 11 oder 12 getränkt sind.13. Melamine resin films or films which are impregnated with the synthetic resin mixture according to claims 11 or 12.
14. Verfahren zum 3D Beschichten, dadurch gekennzeichnet, dass man die Melaminharzfolien und/oder -filme nach Anspruch 13 flächig in einem Arbeitsgang auf die dreidimensionale Struktur eines Werkstoffes aufbringt. 14. A method for 3D coating, characterized in that the melamine resin films and / or films according to claim 13 are applied flatly in one operation to the three-dimensional structure of a material.
15. Verfahren zum 3D Beschichten, dadurch gekennzeichnet, dass man Melaminharzfolien und/oder -filme aus cellulosehaltigen Faserstoffen, die mit der wässrigen Lösung nach den Ansprüchen 1 bis 3 nach- oder vor- und nachgetränkt wurden, herstellt und diese auf die zu beschichtende dreidimensional strukturierte Oberfläche und/oder Formkörper auf-15. A method for 3D coating, characterized in that melamine resin films and / or films made from cellulose-containing fibrous materials which have been post-impregnated or pre-impregnated with the aqueous solution according to claims 1 to 3, and these are three-dimensionally coated onto the one to be coated structured surface and / or molded body
> bringt. > brings.
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE10301901 | 2003-01-17 | ||
| DE2003101901 DE10301901A1 (en) | 2003-01-17 | 2003-01-17 | Aqueous solutions for coating three dimensional cellulosic substrates, used in e.g. the furniture industry, containing a melamine-formaldehyde (MF) condensate, an etherified MF condensate and a polymer dispersion |
| PCT/EP2004/000121 WO2004065484A1 (en) | 2003-01-17 | 2004-01-10 | Use of melamine resin foils and/or films for coating three-dimensionally structured surfaces and/or moulded bodies |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| EP1587870A1 true EP1587870A1 (en) | 2005-10-26 |
Family
ID=32602747
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| EP04701297A Withdrawn EP1587870A1 (en) | 2003-01-17 | 2004-01-10 | Use of melamine resin foils and/or films for coating three-dimensionally structured surfaces and/or moulded bodies |
Country Status (8)
| Country | Link |
|---|---|
| US (1) | US7306842B2 (en) |
| EP (1) | EP1587870A1 (en) |
| JP (1) | JP2006516935A (en) |
| CN (1) | CN100374501C (en) |
| CA (1) | CA2512890A1 (en) |
| DE (1) | DE10301901A1 (en) |
| PL (1) | PL378346A1 (en) |
| WO (1) | WO2004065484A1 (en) |
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|---|---|---|---|---|
| DE102004034528A1 (en) * | 2004-07-15 | 2006-02-16 | Basf Ag | Use of Metaminharzfolien and / or films for 3D coating |
| DE102005035691A1 (en) * | 2005-07-27 | 2007-02-01 | Basf Ag | Aminoplast resin film for coating substrates |
| EP2035112B1 (en) * | 2006-06-20 | 2009-10-28 | Basf Se | Porous material with a nanoporous coating |
| BRPI0806567A2 (en) * | 2007-01-24 | 2014-05-06 | Basf Se | FLEXIBLE FLAT SUBSTRATE WITH AN ABRASIVE SURFACE AND, FLEXIBLE FLAT SUBSTRATE USE |
| US20110130080A1 (en) * | 2008-07-24 | 2011-06-02 | Basf Se | Flexible, flat substrate with an abrasive surface |
| EP2388295A1 (en) | 2010-05-21 | 2011-11-23 | Wietec Technologie KG | Method for producing a transparent plastic material |
| JP6447557B2 (en) * | 2016-03-24 | 2019-01-09 | 日亜化学工業株式会社 | Method for manufacturing light emitting device |
| EP3263561A1 (en) | 2016-06-29 | 2018-01-03 | Borealis Agrolinz Melamine GmbH | Novel triazine precondensate and method for obtaining the same |
| EP3263560A1 (en) | 2016-06-29 | 2018-01-03 | Borealis Agrolinz Melamine GmbH | Novel triazine-precondensate-aldehyde condensation products and method for obtaining the same |
| US20230279613A1 (en) * | 2020-07-10 | 2023-09-07 | Basf Se | Resin-Impregnated Fibrous Material in the Form of a Sheet or a Web |
Family Cites Families (12)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3936547A (en) | 1973-02-24 | 1976-02-03 | Cassella Farbwerke Mainkur Aktiengesellschaft | Process of preparing melamine resin films by impregnation of paper, cellulose, fleece or fabric |
| JPS5113208U (en) | 1974-07-17 | 1976-01-30 | ||
| SE417849B (en) * | 1974-11-20 | 1981-04-13 | Billingsfors Bruks Ab | PROCEDURE FOR MANUFACTURING IMPREGNATED AND COATED WRAPPING |
| JPS6285938A (en) * | 1985-10-11 | 1987-04-20 | 住友ベークライト株式会社 | Melamine-resin decorative board |
| DE3700344A1 (en) * | 1986-10-24 | 1988-04-28 | Cassella Ag | METHOD FOR PRODUCING MELAMINE RESIN FILMS |
| DE3837965A1 (en) * | 1988-11-09 | 1990-05-17 | Basf Ag | HEAT-CURABLE, AQUEOUS RESIN MIXTURES FOR THE COATING OF WOODEN MATERIALS |
| DE4139961A1 (en) * | 1991-12-04 | 1993-06-09 | Basf Ag, 6700 Ludwigshafen, De | RESIN RESIN FOR IMPREGNATING PAPER RAILS |
| DE4439156A1 (en) * | 1994-11-04 | 1996-05-09 | Cassella Ag | Impregnating resins for foils and edges |
| DE19937759A1 (en) * | 1999-08-10 | 2001-02-15 | Basf Ag | Process for the production of panels with a decorative surface |
| JP3789694B2 (en) * | 1999-10-04 | 2006-06-28 | 住友ベークライト株式会社 | Melamine resin decorative sheet |
| DE19954189A1 (en) * | 1999-11-11 | 2001-05-17 | Basf Ag | Melamine resin dispersions |
| EP1136537A1 (en) * | 2000-03-20 | 2001-09-26 | Akzo Nobel N.V. | Adhesive system |
-
2003
- 2003-01-17 DE DE2003101901 patent/DE10301901A1/en not_active Withdrawn
-
2004
- 2004-01-10 WO PCT/EP2004/000121 patent/WO2004065484A1/en not_active Ceased
- 2004-01-10 CA CA 2512890 patent/CA2512890A1/en not_active Abandoned
- 2004-01-10 PL PL37834604A patent/PL378346A1/en not_active Application Discontinuation
- 2004-01-10 JP JP2006500542A patent/JP2006516935A/en active Pending
- 2004-01-10 CN CNB2004800023169A patent/CN100374501C/en not_active Expired - Fee Related
- 2004-01-10 US US10/542,305 patent/US7306842B2/en not_active Expired - Fee Related
- 2004-01-10 EP EP04701297A patent/EP1587870A1/en not_active Withdrawn
Non-Patent Citations (1)
| Title |
|---|
| See references of WO2004065484A1 * |
Also Published As
| Publication number | Publication date |
|---|---|
| US20060051606A1 (en) | 2006-03-09 |
| PL378346A1 (en) | 2006-03-20 |
| CN100374501C (en) | 2008-03-12 |
| CA2512890A1 (en) | 2004-08-05 |
| WO2004065484A1 (en) | 2004-08-05 |
| JP2006516935A (en) | 2006-07-13 |
| DE10301901A1 (en) | 2004-07-29 |
| US7306842B2 (en) | 2007-12-11 |
| CN1738863A (en) | 2006-02-22 |
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