NL8004190A - Werkwijze voor het bekleden van verschillende opper- vlakken en hiervoor geschikte middelen. - Google Patents

Werkwijze voor het bekleden van verschillende opper- vlakken en hiervoor geschikte middelen. Download PDF

Info

Publication number: NL8004190A
Authority: NL; Netherlands
Prior art keywords: resin; resins; vinyl; mixture; mixtures
Prior art date: 1979-08-10

Application number

NL8004190A

Other languages

English (en)

Dutch (nl)

Original Assignee

Anic Spa

Priority date (The priority date 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 date listed.)

1979-08-10

Filing date

1980-07-21

Publication date

1981-02-12

1980-07-21 Application filed by Anic Spa filed Critical Anic Spa

1981-02-12 Publication of NL8004190A publication Critical patent/NL8004190A/nl

Links

238000000034 method Methods 0.000 title claims description 12
239000011248 coating agent Substances 0.000 title claims description 7
238000000576 coating method Methods 0.000 title claims description 7
239000003795 chemical substances by application Substances 0.000 title 1
239000000203 mixture Substances 0.000 claims description 58
239000011347 resin Substances 0.000 claims description 38
229920005989 resin Polymers 0.000 claims description 38
238000004132 cross linking Methods 0.000 claims description 18
150000001875 compounds Chemical class 0.000 claims description 13
239000000463 material Substances 0.000 claims description 9
239000004925 Acrylic resin Substances 0.000 claims description 8
229920000178 Acrylic resin Polymers 0.000 claims description 6
239000004593 Epoxy Substances 0.000 claims description 5
UHESRSKEBRADOO-UHFFFAOYSA-N ethyl carbamate;prop-2-enoic acid Chemical compound OC(=O)C=C.CCOC(N)=O UHESRSKEBRADOO-UHFFFAOYSA-N 0.000 claims description 5
125000000217 alkyl group Chemical group 0.000 claims description 4
125000004432 carbon atom Chemical group C* 0.000 claims description 4
239000003822 epoxy resin Substances 0.000 claims description 4
LNEPOXFFQSENCJ-UHFFFAOYSA-N haloperidol Chemical compound C1CC(O)(C=2C=CC(Cl)=CC=2)CCN1CCCC(=O)C1=CC=C(F)C=C1 LNEPOXFFQSENCJ-UHFFFAOYSA-N 0.000 claims description 4
229920000647 polyepoxide Polymers 0.000 claims description 4
125000003118 aryl group Chemical group 0.000 claims description 3
230000005855 radiation Effects 0.000 claims description 3
229920006337 unsaturated polyester resin Polymers 0.000 claims description 3
125000004429 atom Chemical group 0.000 claims description 2
NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 claims 1
238000010894 electron beam technology Methods 0.000 claims 1
239000000178 monomer Substances 0.000 description 29
JWYVGKFDLWWQJX-UHFFFAOYSA-N 1-ethenylazepan-2-one Chemical compound C=CN1CCCCCC1=O JWYVGKFDLWWQJX-UHFFFAOYSA-N 0.000 description 11
WHNWPMSKXPGLAX-UHFFFAOYSA-N N-Vinyl-2-pyrrolidone Chemical compound C=CN1CCCC1=O WHNWPMSKXPGLAX-UHFFFAOYSA-N 0.000 description 11
239000003085 diluting agent Substances 0.000 description 11
238000010521 absorption reaction Methods 0.000 description 8
PNLUGRYDUHRLOF-UHFFFAOYSA-N n-ethenyl-n-methylacetamide Chemical compound C=CN(C)C(C)=O PNLUGRYDUHRLOF-UHFFFAOYSA-N 0.000 description 8
NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 7
-1 N-vinyl butyltoluenesulfonamide Chemical compound 0.000 description 6
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 6
238000005259 measurement Methods 0.000 description 5
239000003973 paint Substances 0.000 description 5
SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 4
RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 4
238000009835 boiling Methods 0.000 description 4
230000008859 change Effects 0.000 description 3
MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 3
239000003999 initiator Substances 0.000 description 3
229920000728 polyester Polymers 0.000 description 3
MSAHTMIQULFMRG-UHFFFAOYSA-N 1,2-diphenyl-2-propan-2-yloxyethanone Chemical compound C=1C=CC=CC=1C(OC(C)C)C(=O)C1=CC=CC=C1 MSAHTMIQULFMRG-UHFFFAOYSA-N 0.000 description 2
OMIGHNLMNHATMP-UHFFFAOYSA-N 2-hydroxyethyl prop-2-enoate Chemical compound OCCOC(=O)C=C OMIGHNLMNHATMP-UHFFFAOYSA-N 0.000 description 2
MXRGSJAOLKBZLU-UHFFFAOYSA-N 3-ethenylazepan-2-one Chemical compound C=CC1CCCCNC1=O MXRGSJAOLKBZLU-UHFFFAOYSA-N 0.000 description 2
KWOLFJPFCHCOCG-UHFFFAOYSA-N Acetophenone Chemical compound CC(=O)C1=CC=CC=C1 KWOLFJPFCHCOCG-UHFFFAOYSA-N 0.000 description 2
IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
206010022998 Irritability Diseases 0.000 description 2
PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 2
239000000853 adhesive Substances 0.000 description 2
230000001070 adhesive effect Effects 0.000 description 2
150000001991 dicarboxylic acids Chemical class 0.000 description 2
239000000976 ink Substances 0.000 description 2
239000007788 liquid Substances 0.000 description 2
QSHDDOUJBYECFT-UHFFFAOYSA-N mercury Chemical compound [Hg] QSHDDOUJBYECFT-UHFFFAOYSA-N 0.000 description 2
XNGIFLGASWRNHJ-UHFFFAOYSA-N phthalic acid Chemical compound OC(=O)C1=CC=CC=C1C(O)=O XNGIFLGASWRNHJ-UHFFFAOYSA-N 0.000 description 2
229920003023 plastic Polymers 0.000 description 2
239000004033 plastic Substances 0.000 description 2
238000006116 polymerization reaction Methods 0.000 description 2
239000000758 substrate Substances 0.000 description 2
229920002803 thermoplastic polyurethane Polymers 0.000 description 2
231100000419 toxicity Toxicity 0.000 description 2
230000001988 toxicity Effects 0.000 description 2
229920002554 vinyl polymer Polymers 0.000 description 2
239000002023 wood Substances 0.000 description 2
229920002818 (Hydroxyethyl)methacrylate Polymers 0.000 description 1
RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 description 1
PBGPBHYPCGDFEZ-UHFFFAOYSA-N 1-ethenylpiperidin-2-one Chemical compound C=CN1CCCCC1=O PBGPBHYPCGDFEZ-UHFFFAOYSA-N 0.000 description 1
UFHGCLDQEUUPLD-UHFFFAOYSA-N 1-phenylhept-6-ene-1-sulfonamide Chemical compound C(=C)CCCCC(C1=CC=CC=C1)S(=O)(=O)N UFHGCLDQEUUPLD-UHFFFAOYSA-N 0.000 description 1
KWVGIHKZDCUPEU-UHFFFAOYSA-N 2,2-dimethoxy-2-phenylacetophenone Chemical compound C=1C=CC=CC=1C(OC)(OC)C(=O)C1=CC=CC=C1 KWVGIHKZDCUPEU-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
KMNCBSZOIQAUFX-UHFFFAOYSA-N 2-ethoxy-1,2-diphenylethanone Chemical compound C=1C=CC=CC=1C(OCC)C(=O)C1=CC=CC=C1 KMNCBSZOIQAUFX-UHFFFAOYSA-N 0.000 description 1
BQZJOQXSCSZQPS-UHFFFAOYSA-N 2-methoxy-1,2-diphenylethanone Chemical compound C=1C=CC=CC=1C(OC)C(=O)C1=CC=CC=C1 BQZJOQXSCSZQPS-UHFFFAOYSA-N 0.000 description 1
SUAYFRHPQLERMW-UHFFFAOYSA-N 2-methyl-1,2-diphenylpropan-1-one Chemical compound C=1C=CC=CC=1C(C)(C)C(=O)C1=CC=CC=C1 SUAYFRHPQLERMW-UHFFFAOYSA-N 0.000 description 1
KCDIHKAXKRTRMU-UHFFFAOYSA-N 2-methyl-n-prop-2-enylpropanamide Chemical compound CC(C)C(=O)NCC=C KCDIHKAXKRTRMU-UHFFFAOYSA-N 0.000 description 1
206010001497 Agitation Diseases 0.000 description 1
LCFVJGUPQDGYKZ-UHFFFAOYSA-N Bisphenol A diglycidyl ether Chemical compound C=1C=C(OCC2OC2)C=CC=1C(C)(C)C(C=C1)=CC=C1OCC1CO1 LCFVJGUPQDGYKZ-UHFFFAOYSA-N 0.000 description 1
JBKVHLHDHHXQEQ-UHFFFAOYSA-N Caprolactam Natural products O=C1CCCCCN1 JBKVHLHDHHXQEQ-UHFFFAOYSA-N 0.000 description 1
239000005057 Hexamethylene diisocyanate Substances 0.000 description 1
WOBHKFSMXKNTIM-UHFFFAOYSA-N Hydroxyethyl methacrylate Chemical compound CC(=C)C(=O)OCCO WOBHKFSMXKNTIM-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
MGJKQDOBUOMPEZ-UHFFFAOYSA-N N,N'-dimethylurea Chemical compound CNC(=O)NC MGJKQDOBUOMPEZ-UHFFFAOYSA-N 0.000 description 1
YCQLCWDNVYPCSU-UHFFFAOYSA-N N-hex-5-enyl-1-phenylmethanesulfonamide Chemical compound C(=C)CCCCNS(=O)(=O)CC1=CC=CC=C1 YCQLCWDNVYPCSU-UHFFFAOYSA-N 0.000 description 1
LGRFSURHDFAFJT-UHFFFAOYSA-N Phthalic anhydride Natural products C1=CC=C2C(=O)OC(=O)C2=C1 LGRFSURHDFAFJT-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
229910000831 Steel Inorganic materials 0.000 description 1
239000002253 acid Substances 0.000 description 1
239000000654 additive Substances 0.000 description 1
125000002723 alicyclic group Chemical group 0.000 description 1
125000001931 aliphatic group Chemical group 0.000 description 1
150000001336 alkenes Chemical class 0.000 description 1
PYKYMHQGRFAEBM-UHFFFAOYSA-N anthraquinone Natural products CCC(=O)c1c(O)c2C(=O)C3C(C=CC=C3O)C(=O)c2cc1CC(=O)OC PYKYMHQGRFAEBM-UHFFFAOYSA-N 0.000 description 1
150000004056 anthraquinones Chemical class 0.000 description 1
WURBFLDFSFBTLW-UHFFFAOYSA-N benzil Chemical compound C=1C=CC=CC=1C(=O)C(=O)C1=CC=CC=C1 WURBFLDFSFBTLW-UHFFFAOYSA-N 0.000 description 1
WPYMKLBDIGXBTP-UHFFFAOYSA-N benzoic acid group Chemical group C(C1=CC=CC=C1)(=O)O WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 description 1
RWCCWEUUXYIKHB-UHFFFAOYSA-N benzophenone Chemical compound C=1C=CC=CC=1C(=O)C1=CC=CC=C1 RWCCWEUUXYIKHB-UHFFFAOYSA-N 0.000 description 1
239000012965 benzophenone Substances 0.000 description 1
JHIWVOJDXOSYLW-UHFFFAOYSA-N butyl 2,2-difluorocyclopropane-1-carboxylate Chemical compound CCCCOC(=O)C1CC1(F)F JHIWVOJDXOSYLW-UHFFFAOYSA-N 0.000 description 1
CQEYYJKEWSMYFG-UHFFFAOYSA-N butyl acrylate Chemical compound CCCCOC(=O)C=C CQEYYJKEWSMYFG-UHFFFAOYSA-N 0.000 description 1
238000010538 cationic polymerization reaction Methods 0.000 description 1
238000006243 chemical reaction Methods 0.000 description 1
238000011161 development Methods 0.000 description 1
125000005442 diisocyanate group Chemical group 0.000 description 1
238000005265 energy consumption Methods 0.000 description 1
150000002334 glycols Chemical class 0.000 description 1
RRAMGCGOFNQTLD-UHFFFAOYSA-N hexamethylene diisocyanate Chemical compound O=C=NCCCCCCN=C=O RRAMGCGOFNQTLD-UHFFFAOYSA-N 0.000 description 1
125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
230000001678 irradiating effect Effects 0.000 description 1
239000004922 lacquer 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
238000012986 modification Methods 0.000 description 1
230000004048 modification Effects 0.000 description 1
DSGQWDHZUIZVCR-UHFFFAOYSA-N n-but-3-enylacetamide Chemical compound CC(=O)NCCC=C DSGQWDHZUIZVCR-UHFFFAOYSA-N 0.000 description 1
NTLLWXVIHDZMLL-UHFFFAOYSA-N n-butyl-n-ethenyl-4-methylbenzenesulfonamide Chemical compound CCCCN(C=C)S(=O)(=O)C1=CC=C(C)C=C1 NTLLWXVIHDZMLL-UHFFFAOYSA-N 0.000 description 1
IQVLNQNLISXIOS-UHFFFAOYSA-N n-ethenyl-2-phenylacetamide Chemical compound C=CNC(=O)CC1=CC=CC=C1 IQVLNQNLISXIOS-UHFFFAOYSA-N 0.000 description 1
KNFILXSWEXSJCV-UHFFFAOYSA-N n-ethenyl-n,4-dimethylbenzenesulfonamide Chemical compound C=CN(C)S(=O)(=O)C1=CC=C(C)C=C1 KNFILXSWEXSJCV-UHFFFAOYSA-N 0.000 description 1
KGQOXHDHWAZUPT-UHFFFAOYSA-N n-ethenyl-n-methylbenzamide Chemical compound C=CN(C)C(=O)C1=CC=CC=C1 KGQOXHDHWAZUPT-UHFFFAOYSA-N 0.000 description 1
WTQKCSHGGMGBDC-UHFFFAOYSA-N n-ethenyl-n-methylbutanamide Chemical compound CCCC(=O)N(C)C=C WTQKCSHGGMGBDC-UHFFFAOYSA-N 0.000 description 1
RXLDPCKXDHZZQC-UHFFFAOYSA-N n-ethenylpentanamide Chemical compound CCCCC(=O)NC=C RXLDPCKXDHZZQC-UHFFFAOYSA-N 0.000 description 1
UJQMPESLHUQZRP-UHFFFAOYSA-N n-hex-5-enyl-4-methylbenzenesulfonamide Chemical compound CC1=CC=C(S(=O)(=O)NCCCCC=C)C=C1 UJQMPESLHUQZRP-UHFFFAOYSA-N 0.000 description 1
PMGNVDPARHYFIN-UHFFFAOYSA-N n-methylbut-3-en-2-amine Chemical compound CNC(C)C=C PMGNVDPARHYFIN-UHFFFAOYSA-N 0.000 description 1
229910052757 nitrogen Inorganic materials 0.000 description 1
239000012299 nitrogen atmosphere Substances 0.000 description 1
230000009965 odorless effect Effects 0.000 description 1
JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 description 1
238000010422 painting Methods 0.000 description 1
229920001225 polyester resin Polymers 0.000 description 1
239000004645 polyester resin Substances 0.000 description 1
229920000642 polymer Polymers 0.000 description 1
230000008092 positive effect Effects 0.000 description 1
238000002360 preparation method Methods 0.000 description 1
230000008569 process Effects 0.000 description 1
KCTAWXVAICEBSD-UHFFFAOYSA-N prop-2-enoyloxy prop-2-eneperoxoate Chemical compound C=CC(=O)OOOC(=O)C=C KCTAWXVAICEBSD-UHFFFAOYSA-N 0.000 description 1
238000010526 radical polymerization reaction Methods 0.000 description 1
230000009257 reactivity Effects 0.000 description 1
229920006395 saturated elastomer Polymers 0.000 description 1
239000007787 solid Substances 0.000 description 1
239000002904 solvent Substances 0.000 description 1
239000010959 steel Substances 0.000 description 1
238000012360 testing method Methods 0.000 description 1
230000002588 toxic effect Effects 0.000 description 1
231100000563 toxic property Toxicity 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
238000009281 ultraviolet germicidal irradiation Methods 0.000 description 1
230000004584 weight gain Effects 0.000 description 1
235000019786 weight gain Nutrition 0.000 description 1
230000004580 weight loss Effects 0.000 description 1

Classifications

- B—PERFORMING OPERATIONS; TRANSPORTING
- B05—SPRAYING OR ATOMISING IN GENERAL; APPLYING FLUENT MATERIALS TO SURFACES, IN GENERAL
- B05D—PROCESSES FOR APPLYING FLUENT MATERIALS TO SURFACES, IN GENERAL
- B05D7/00—Processes, other than flocking, specially adapted for applying liquids or other fluent materials to particular surfaces or for applying particular liquids or other fluent materials
- B05D7/24—Processes, other than flocking, specially adapted for applying liquids or other fluent materials to particular surfaces or for applying particular liquids or other fluent materials for applying particular liquids or other fluent materials
- 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
- C08F299/00—Macromolecular compounds obtained by interreacting polymers involving only carbon-to-carbon unsaturated bond reactions, in the absence of non-macromolecular monomers
- C08F299/02—Macromolecular compounds obtained by interreacting polymers involving only carbon-to-carbon unsaturated bond reactions, in the absence of non-macromolecular monomers from unsaturated polycondensates
- 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
- C08F299/00—Macromolecular compounds obtained by interreacting polymers involving only carbon-to-carbon unsaturated bond reactions, in the absence of non-macromolecular monomers
- C08F299/02—Macromolecular compounds obtained by interreacting polymers involving only carbon-to-carbon unsaturated bond reactions, in the absence of non-macromolecular monomers from unsaturated polycondensates
- C08F299/022—Macromolecular compounds obtained by interreacting polymers involving only carbon-to-carbon unsaturated bond reactions, in the absence of non-macromolecular monomers from unsaturated polycondensates from polycondensates with side or terminal unsaturations
- C08F299/024—Macromolecular compounds obtained by interreacting polymers involving only carbon-to-carbon unsaturated bond reactions, in the absence of non-macromolecular monomers from unsaturated polycondensates from polycondensates with side or terminal unsaturations the unsaturation being in acrylic or methacrylic groups
- 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
- C08F299/00—Macromolecular compounds obtained by interreacting polymers involving only carbon-to-carbon unsaturated bond reactions, in the absence of non-macromolecular monomers
- C08F299/02—Macromolecular compounds obtained by interreacting polymers involving only carbon-to-carbon unsaturated bond reactions, in the absence of non-macromolecular monomers from unsaturated polycondensates
- C08F299/026—Macromolecular compounds obtained by interreacting polymers involving only carbon-to-carbon unsaturated bond reactions, in the absence of non-macromolecular monomers from unsaturated polycondensates from the reaction products of polyepoxides and unsaturated monocarboxylic acids, their anhydrides, halogenides or esters with low molecular weight
- C08F299/028—Macromolecular compounds obtained by interreacting polymers involving only carbon-to-carbon unsaturated bond reactions, in the absence of non-macromolecular monomers from unsaturated polycondensates from the reaction products of polyepoxides and unsaturated monocarboxylic acids, their anhydrides, halogenides or esters with low molecular weight photopolymerisable compositions
- 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
- C08F299/00—Macromolecular compounds obtained by interreacting polymers involving only carbon-to-carbon unsaturated bond reactions, in the absence of non-macromolecular monomers
- C08F299/02—Macromolecular compounds obtained by interreacting polymers involving only carbon-to-carbon unsaturated bond reactions, in the absence of non-macromolecular monomers from unsaturated polycondensates
- C08F299/04—Macromolecular compounds obtained by interreacting polymers involving only carbon-to-carbon unsaturated bond reactions, in the absence of non-macromolecular monomers from unsaturated polycondensates from polyesters
- C08F299/0478—Copolymers from unsaturated polyesters and low molecular monomers characterised by the monomers used
- 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
- C08F299/00—Macromolecular compounds obtained by interreacting polymers involving only carbon-to-carbon unsaturated bond reactions, in the absence of non-macromolecular monomers
- C08F299/02—Macromolecular compounds obtained by interreacting polymers involving only carbon-to-carbon unsaturated bond reactions, in the absence of non-macromolecular monomers from unsaturated polycondensates
- C08F299/04—Macromolecular compounds obtained by interreacting polymers involving only carbon-to-carbon unsaturated bond reactions, in the absence of non-macromolecular monomers from unsaturated polycondensates from polyesters
- C08F299/0485—Macromolecular compounds obtained by interreacting polymers involving only carbon-to-carbon unsaturated bond reactions, in the absence of non-macromolecular monomers from unsaturated polycondensates from polyesters from polyesters with side or terminal unsaturations
- 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
- C08F299/00—Macromolecular compounds obtained by interreacting polymers involving only carbon-to-carbon unsaturated bond reactions, in the absence of non-macromolecular monomers
- C08F299/02—Macromolecular compounds obtained by interreacting polymers involving only carbon-to-carbon unsaturated bond reactions, in the absence of non-macromolecular monomers from unsaturated polycondensates
- C08F299/06—Macromolecular compounds obtained by interreacting polymers involving only carbon-to-carbon unsaturated bond reactions, in the absence of non-macromolecular monomers from unsaturated polycondensates from polyurethanes
- 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
- C09D4/00—Coating compositions, e.g. paints, varnishes or lacquers, based on organic non-macromolecular compounds having at least one polymerisable carbon-to-carbon unsaturated bond ; Coating compositions, based on monomers of macromolecular compounds of groups C09D183/00 - C09D183/16
- 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
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S525/00—Synthetic resins or natural rubbers -- part of the class 520 series
- Y10S525/92—Polyurethane having terminal ethylenic unsaturation
- 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
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S525/00—Synthetic resins or natural rubbers -- part of the class 520 series
- Y10S525/922—Polyepoxide polymer having been reacted to yield terminal ethylenic unsaturation

Landscapes

Chemical & Material Sciences (AREA)
Organic Chemistry (AREA)
Health & Medical Sciences (AREA)
Chemical Kinetics & Catalysis (AREA)
Medicinal Chemistry (AREA)
Polymers & Plastics (AREA)
Life Sciences & Earth Sciences (AREA)
Engineering & Computer Science (AREA)
Wood Science & Technology (AREA)
Materials Engineering (AREA)
Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
Macromonomer-Based Addition Polymer (AREA)
Paints Or Removers (AREA)
Adhesives Or Adhesive Processes (AREA)
Application Of Or Painting With Fluid Materials (AREA)
Polymerisation Methods In General (AREA)
Inks, Pencil-Leads, Or Crayons (AREA)

NL8004190A 1979-08-10 1980-07-21 Werkwijze voor het bekleden van verschillende opper- vlakken en hiervoor geschikte middelen. NL8004190A (nl)

Applications Claiming Priority (2)

Application Number	Priority Date	Filing Date	Title
IT2505079		1979-08-10
IT25050/79A IT1162770B (it)	1979-08-10	1979-08-10	Metodo per ricoprire superfici varie e mezzi adatti allo scopo

Publications (1)

Publication Number	Publication Date
NL8004190A true NL8004190A (nl)	1981-02-12

Family

ID=11215540

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
NL8004190A NL8004190A (nl)	1979-08-10	1980-07-21	Werkwijze voor het bekleden van verschillende opper- vlakken en hiervoor geschikte middelen.

Country Status (9)

Country	Link
US (1)	US4348427A (fr)
JP (1)	JPS5626918A (fr)
BE (1)	BE884395A (fr)
DE (1)	DE3027574C2 (fr)
DK (1)	DK297480A (fr)
FR (1)	FR2463168A1 (fr)
GB (1)	GB2055860B (fr)
IT (1)	IT1162770B (fr)
NL (1)	NL8004190A (fr)

Families Citing this family (31)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
JPS5667322A (en) *	1979-11-05	1981-06-06	Showa Highpolymer Co Ltd	Curable resin composition
IT1141029B (it) *	1980-08-29	1986-10-01	Anic Spa	Composizione a base di policarbonato avente proprieta' migliorate e metodo per il suo ottenimento
US4425208A (en)	1981-08-06	1984-01-10	The Upjohn Company	Compositions and process
US4446247A (en) *	1981-08-06	1984-05-01	The Upjohn Company	Compositions and process
US4518473A (en) *	1981-08-06	1985-05-21	The Upjohn Company	Compositions and process
US4465806A (en) *	1981-09-08	1984-08-14	Plastics Engineering Company	Unsaturated polyester molding compounds with improved resistance to thermal and humid aging
US4472019A (en) *	1982-12-28	1984-09-18	Desoto, Inc.	Topcoats for buffer-coated optical fiber using urethane acrylate and epoxy acrylate and vinyl monomer
US4824919A (en) *	1983-06-09	1989-04-25	The Dow Chemical Company	Toughening of cured vinyl ester resins by inclusion in the uncured resins of oligomeric vinyl-reactive urethanes which phase out upon curing
US4851490A (en) *	1983-10-26	1989-07-25	Betz Laboratories, Inc.	Water soluble phosphonated polymers
US4522465A (en) *	1983-11-10	1985-06-11	Desoto, Inc.	Optical fiber coated with an ultraviolet cured topcoating
AU590742B2 (en) *	1984-02-11	1989-11-16	Kulzer Gmbh	Method for producing orthodontic devices and appliances
DE3404904C2 (de) *	1984-02-11	1986-01-16	Kulzer & Co GmbH, 6393 Wehrheim	Verfahren zur Herstellung von kieferorthopädischen Geräten und Apparaturen
JPS60199012A (ja) *	1984-03-24	1985-10-08	Toomee Sangyo Kk	コンタクトレンズ材料
US4738870A (en) *	1986-03-27	1988-04-19	The Dow Chemical Company	Adherent photopolymerizable compositions
JP2573661B2 (ja) *	1988-07-09	1997-01-22	キヤノン株式会社	感光感熱型接着剤
US5212271A (en) *	1989-12-22	1993-05-18	Texaco Chemical Company	Process for obtaining textured coatings from photo-curable urea-containing compositions
US5418016A (en) *	1991-03-03	1995-05-23	Air Products And Chemicals, Inc.	Coating process using radiation curable compositions
GB2264118B (en) †	1992-02-07	1996-01-10	Sericol Ltd	Radiation-curable compositions
US5281682A (en) *	1992-03-03	1994-01-25	Air Products And Chemicals, Inc.	Radiation curable compositions and method of use
DE4228401A1 (de) *	1992-08-26	1994-03-03	Basf Lacke & Farben	Pulverlacke
US5463110A (en) *	1994-05-20	1995-10-31	Air Products And Chemicals, Inc.	Michael adducts of N-vinylformamide and acrylic and methacrylic esters
US5672731A (en) *	1994-05-20	1997-09-30	Air Products And Chemicals, Inc.	N-vinylformamide/alkyl acrylate Michael adducts
US5569725A (en) *	1994-10-14	1996-10-29	Air Products And Chemicals, Inc.	N-vinyl-n-acyl urea resins
US5728878A (en) *	1996-07-02	1998-03-17	Air Products And Chemicals, Inc.	Functional N-vinylformamides
GB2358869B (en) *	1999-01-08	2003-11-26	Loctite	Adhesion promoters
US20040010111A1 (en) *	2000-12-15	2004-01-15	Birkett David P.	Adhesives for dvd bonding
US7431759B2 (en) *	2005-03-31	2008-10-07	Sloan Donald D	High elongation vacuum formable digital ink
US7662224B2 (en) *	2005-03-31	2010-02-16	Sloan Donald D	High elongation vacuum formable digital ink
US7427317B2 (en) *	2005-03-31	2008-09-23	Sloan Donald D	High elongation vacuum formable digital ink
JP5089770B2 (ja) *	2007-05-01	2012-12-05	エグザテック・リミテッド・ライアビリティー・カンパニー	Ｕｖ硬化性印刷パターンを有するプラスチックグレージングパネル及びそのパネルを作製する方法
US20110209901A1 (en) *	2007-08-02	2011-09-01	Dupont Teijin Films U.S. Limited Partnership	Coated polyester film

Family Cites Families (6)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
DE1060590B (de) *	1957-08-27	1959-07-02	Basf Ag	Verfahren zur Herstellung von Formkoerpern und UEberzuegen
US3008918A (en) *	1958-01-29	1961-11-14	Dow Chemical Co	Compositions comprising graft copolymers of certain sulfonated acrylate and acryloyl taurine type monomers on acrylonitrile polymer substrates
DE2049715C3 (de) *	1970-10-09	1978-06-22	Basf Farben + Fasern Ag, 2000 Hamburg	Verfahren zur Herstellung von durch ionisierende Strahlung gehärteten Filmen und Überzügen
US3870768A (en) *	1971-09-15	1975-03-11	Stepan Chemical Co	Unsaturated amides of oxybis(benzenesulfonic acid) and their use as cross-linking agents
DE2441148C2 (de) *	1974-08-28	1982-10-14	Basf Ag, 6700 Ludwigshafen	Strahlungshärtbare Überzugsmasse
US4205139A (en) *	1974-08-28	1980-05-27	Basf Aktiengesellschaft	Curable coating composition

1979
- 1979-08-10 IT IT25050/79A patent/IT1162770B/it active
1980
- 1980-07-10 DK DK297480A patent/DK297480A/da not_active Application Discontinuation
- 1980-07-11 US US06/167,701 patent/US4348427A/en not_active Expired - Lifetime
- 1980-07-16 GB GB8023240A patent/GB2055860B/en not_active Expired
- 1980-07-17 FR FR8015827A patent/FR2463168A1/fr active Granted
- 1980-07-18 BE BE0/201468A patent/BE884395A/fr not_active IP Right Cessation
- 1980-07-21 NL NL8004190A patent/NL8004190A/nl not_active Application Discontinuation
- 1980-07-21 DE DE3027574A patent/DE3027574C2/de not_active Expired
- 1980-07-21 JP JP9886080A patent/JPS5626918A/ja active Pending

Also Published As

Publication number	Publication date
FR2463168B1 (fr)	1983-02-04
GB2055860A (en)	1981-03-11
DK297480A (da)	1981-02-11
JPS5626918A (en)	1981-03-16
BE884395A (fr)	1981-01-19
DE3027574A1 (de)	1981-02-19
DE3027574C2 (de)	1982-09-16
FR2463168A1 (fr)	1981-02-20
IT1162770B (it)	1987-04-01
IT7925050A0 (it)	1979-08-10
US4348427A (en)	1982-09-07
GB2055860B (en)	1983-01-12

Legal Events

Date	Code	Title
1980-12-29	BATV	A request for search has been withdrawn
1985-01-01	A85	Still pending on 85-01-01
1987-03-02	BV	The patent application has lapsed

Publication	Publication Date	Title
NL8004190A (nl)	1981-02-12	Werkwijze voor het bekleden van verschillende opper- vlakken en hiervoor geschikte middelen.
US4022674A (en)	1977-05-10	Photopolymerizable compounds and compositions comprising the product of the reaction of a monomeric ester and a polycarboxy-substituted benzophenone
US3926641A (en)	1975-12-16	Photopolymerizable compositions comprising polycarboxysubstituted benzophenone reaction products
US4004998A (en)	1977-01-25	Photopolymerizable compounds and compositions comprising the product of the reaction of a hydroxy-containing ester and a monocarboxy-substituted benzophenone
US4048034A (en)	1977-09-13	Photopolymerization using an alpha-aminoacetophenone
US3551235A (en)	1970-12-29	Radiation-curable compositions
US3551311A (en)	1970-12-29	Radiation-curable compositions
US5629359A (en)	1997-05-13	Radiation curable compositions
CA1047683A (fr)	1979-01-30	Composes photopolymerisables non satures en position ethylene
CA2126833C (fr)	1999-11-30	Procede de revetement utilisant des compositions photoreticulables
JP2001506693A (ja)	2001-05-22	放射線架橋性高分子アクリラートまたはメタクリラートの製造法
US3968016A (en)	1976-07-06	Mixture of unsaturated polyester resins with an epoxy diacrylate and the actinic light treatment of same
US4235981A (en)	1980-11-25	Coating compositions
US4067791A (en)	1978-01-10	Ultraviolet light curable coating compositions
US3783151A (en)	1974-01-01	Isocyanate-modified esters
EP0906351B1 (fr)	2002-09-04	Composition de polyester photopolymerisable et son procede de preparation
US4104144A (en)	1978-08-01	Radiation-curable coating compositions and inks
JP3409595B2 (ja)	2003-05-26	活性エネルギー線硬化型組成物
CA1163746A (fr)	1984-03-13	COMPOSITIONS RENFERMANT DES ACRYLATES DE .beta.- CYANOETHOXYALKYLE, RETICULABLES A LA LUMIERE
US3945833A (en)	1976-03-23	Photosensitive coating composition
US3926640A (en)	1975-12-16	Photopolymerizable compositions comprising benzophenone reaction products
WO2001072858A1 (fr)	2001-10-04	Composition
JPS61130337A (ja)	1986-06-18	エチレン性不飽和ポリエステル
JPH01131223A (ja)	1989-05-24	活性エネルギー線硬化性樹脂組成物並びに被覆組成物および印刷インキ組成物
US4180599A (en)	1979-12-25	Crosslinking photoinitiators of acrylic benzophenonetetracarboxylates