NO792123L - Herdbare sammensetninger for oppnaaelse av overflater med lav glans - Google Patents

Herdbare sammensetninger for oppnaaelse av overflater med lav glans

Info

Publication number: NO792123L
Authority: NO; Norway
Prior art keywords: compound; reactive; intensity level; composition; oxygen
Prior art date: 1978-06-26

Application number

NO792123A

Other languages

English (en)

Norwegian (no)

Inventor

John Robert Mcdowell

Original Assignee

Lord Corp

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.)

1978-06-26

Filing date

1979-06-25

Publication date

1979-12-28

1979-06-25 Application filed by Lord Corp filed Critical Lord Corp

1979-12-28 Publication of NO792123L publication Critical patent/NO792123L/no

Links

239000000203 mixture Substances 0.000 title claims description 78
150000001875 compounds Chemical class 0.000 claims description 77
VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims description 47
QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 40
239000001301 oxygen Substances 0.000 claims description 40
229910052760 oxygen Inorganic materials 0.000 claims description 40
239000003085 diluting agent Substances 0.000 claims description 36
230000002165 photosensitisation Effects 0.000 claims description 36
239000003504 photosensitizing agent Substances 0.000 claims description 35
239000012298 atmosphere Substances 0.000 claims description 32
-1 radical compounds Chemical class 0.000 claims description 30
150000003254 radicals Chemical group 0.000 claims description 28
238000000034 method Methods 0.000 claims description 27
239000000377 silicon dioxide Substances 0.000 claims description 22
235000012239 silicon dioxide Nutrition 0.000 claims description 22
239000011941 photocatalyst Substances 0.000 claims description 21
230000005764 inhibitory process Effects 0.000 claims description 13
RWCCWEUUXYIKHB-UHFFFAOYSA-N benzophenone Chemical compound C=1C=CC=CC=1C(=O)C1=CC=CC=C1 RWCCWEUUXYIKHB-UHFFFAOYSA-N 0.000 claims description 10
239000012965 benzophenone Substances 0.000 claims description 10
239000000178 monomer Substances 0.000 claims description 10
239000008199 coating composition Substances 0.000 claims description 9
238000010526 radical polymerization reaction Methods 0.000 claims description 9
239000000654 additive Substances 0.000 claims description 7
230000005284 excitation Effects 0.000 claims description 7
230000015572 biosynthetic process Effects 0.000 claims description 6
230000005855 radiation Effects 0.000 claims description 6
238000006356 dehydrogenation reaction Methods 0.000 claims description 5
238000004519 manufacturing process Methods 0.000 claims description 5
DKEGCUDAFWNSSO-UHFFFAOYSA-N 1,8-dibromooctane Chemical compound BrCCCCCCCCBr DKEGCUDAFWNSSO-UHFFFAOYSA-N 0.000 claims description 4
238000006897 homolysis reaction Methods 0.000 claims description 4
238000006552 photochemical reaction Methods 0.000 claims description 4
230000001443 photoexcitation Effects 0.000 claims description 4
PIZHFBODNLEQBL-UHFFFAOYSA-N 2,2-diethoxy-1-phenylethanone Chemical compound CCOC(OCC)C(=O)C1=CC=CC=C1 PIZHFBODNLEQBL-UHFFFAOYSA-N 0.000 claims description 2
238000012682 free radical photopolymerization Methods 0.000 claims 2
239000010408 film Substances 0.000 description 45
238000000576 coating method Methods 0.000 description 44
239000011248 coating agent Substances 0.000 description 32
238000001723 curing Methods 0.000 description 23
125000004432 carbon atom Chemical group C* 0.000 description 21
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125000000217 alkyl group Chemical group 0.000 description 17
239000003795 chemical substances by application Substances 0.000 description 15
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125000004435 hydrogen atom Chemical group [H]* 0.000 description 13
229920000642 polymer Polymers 0.000 description 13
125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 11
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239000001257 hydrogen Substances 0.000 description 10
229910052739 hydrogen Inorganic materials 0.000 description 10
125000002887 hydroxy group Chemical group [H]O* 0.000 description 9
238000006116 polymerization reaction Methods 0.000 description 9
PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 8
239000012948 isocyanate Substances 0.000 description 8
230000009467 reduction Effects 0.000 description 8
NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 7
125000003545 alkoxy group Chemical group 0.000 description 7
QSHDDOUJBYECFT-UHFFFAOYSA-N mercury Chemical compound [Hg] QSHDDOUJBYECFT-UHFFFAOYSA-N 0.000 description 7
229920001228 polyisocyanate Polymers 0.000 description 7
239000005056 polyisocyanate Substances 0.000 description 7
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IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 6
238000006243 chemical reaction Methods 0.000 description 6
150000002431 hydrogen Chemical class 0.000 description 6
239000000758 substrate Substances 0.000 description 6
238000012644 addition polymerization Methods 0.000 description 5
150000002148 esters Chemical class 0.000 description 5
229910052736 halogen Inorganic materials 0.000 description 5
150000002367 halogens Chemical class 0.000 description 5
IQPQWNKOIGAROB-UHFFFAOYSA-N isocyanate group Chemical group [N-]=C=O IQPQWNKOIGAROB-UHFFFAOYSA-N 0.000 description 5
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 5
239000000049 pigment Substances 0.000 description 5
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125000001931 aliphatic group Chemical group 0.000 description 4
125000003118 aryl group Chemical group 0.000 description 4
239000011230 binding agent Substances 0.000 description 4
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150000002734 metacrylic acid derivatives Chemical class 0.000 description 4
230000001105 regulatory effect Effects 0.000 description 4
239000002344 surface layer Substances 0.000 description 4
238000012360 testing method Methods 0.000 description 4
SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 3
QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
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YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
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230000008901 benefit Effects 0.000 description 3
125000000753 cycloalkyl group Chemical group 0.000 description 3
230000008020 evaporation Effects 0.000 description 3
239000000945 filler Substances 0.000 description 3
230000004907 flux Effects 0.000 description 3
235000011187 glycerol Nutrition 0.000 description 3
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239000004615 ingredient Substances 0.000 description 3
230000005865 ionizing radiation Effects 0.000 description 3
230000007246 mechanism Effects 0.000 description 3
229910052757 nitrogen Inorganic materials 0.000 description 3
239000002245 particle Substances 0.000 description 3
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238000002360 preparation method Methods 0.000 description 3
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DVKJHBMWWAPEIU-UHFFFAOYSA-N toluene 2,4-diisocyanate Chemical compound CC1=CC=C(N=C=O)C=C1N=C=O DVKJHBMWWAPEIU-UHFFFAOYSA-N 0.000 description 3
150000003673 urethanes Chemical class 0.000 description 3
239000002966 varnish Substances 0.000 description 3
PUPZLCDOIYMWBV-UHFFFAOYSA-N (+/-)-1,3-Butanediol Chemical compound CC(O)CCO PUPZLCDOIYMWBV-UHFFFAOYSA-N 0.000 description 2
UNVGBIALRHLALK-UHFFFAOYSA-N 1,5-Hexanediol Chemical compound CC(O)CCCCO UNVGBIALRHLALK-UHFFFAOYSA-N 0.000 description 2
LEJBBGNFPAFPKQ-UHFFFAOYSA-N 2-(2-prop-2-enoyloxyethoxy)ethyl prop-2-enoate Chemical compound C=CC(=O)OCCOCCOC(=O)C=C LEJBBGNFPAFPKQ-UHFFFAOYSA-N 0.000 description 2
GOXQRTZXKQZDDN-UHFFFAOYSA-N 2-Ethylhexyl acrylate Chemical compound CCCCC(CC)COC(=O)C=C GOXQRTZXKQZDDN-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
KUDUQBURMYMBIJ-UHFFFAOYSA-N 2-prop-2-enoyloxyethyl prop-2-enoate Chemical compound C=CC(=O)OCCOC(=O)C=C KUDUQBURMYMBIJ-UHFFFAOYSA-N 0.000 description 2
DKIDEFUBRARXTE-UHFFFAOYSA-M 3-mercaptopropionate Chemical compound [O-]C(=O)CCS DKIDEFUBRARXTE-UHFFFAOYSA-M 0.000 description 2
CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 2
239000004925 Acrylic resin Substances 0.000 description 2
229920000178 Acrylic resin Polymers 0.000 description 2
HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 2
RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 2
YNQLUTRBYVCPMQ-UHFFFAOYSA-N Ethylbenzene Chemical compound CCC1=CC=CC=C1 YNQLUTRBYVCPMQ-UHFFFAOYSA-N 0.000 description 2
239000005058 Isophorone diisocyanate Substances 0.000 description 2
YNAVUWVOSKDBBP-UHFFFAOYSA-N Morpholine Chemical compound C1COCCN1 YNAVUWVOSKDBBP-UHFFFAOYSA-N 0.000 description 2
IMNFDUFMRHMDMM-UHFFFAOYSA-N N-Heptane Chemical compound CCCCCCC IMNFDUFMRHMDMM-UHFFFAOYSA-N 0.000 description 2
239000004952 Polyamide Chemical class 0.000 description 2
PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 2
ZJCCRDAZUWHFQH-UHFFFAOYSA-N Trimethylolpropane Chemical compound CCC(CO)(CO)CO ZJCCRDAZUWHFQH-UHFFFAOYSA-N 0.000 description 2
WNLRTRBMVRJNCN-UHFFFAOYSA-N adipic acid Chemical compound OC(=O)CCCCC(O)=O WNLRTRBMVRJNCN-UHFFFAOYSA-N 0.000 description 2
XXROGKLTLUQVRX-UHFFFAOYSA-N allyl alcohol Chemical compound OCC=C XXROGKLTLUQVRX-UHFFFAOYSA-N 0.000 description 2
229910052782 aluminium Inorganic materials 0.000 description 2
XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 2
230000009286 beneficial effect Effects 0.000 description 2
125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 description 2
HQABUPZFAYXKJW-UHFFFAOYSA-N butan-1-amine Chemical compound CCCCN HQABUPZFAYXKJW-UHFFFAOYSA-N 0.000 description 2
WERYXYBDKMZEQL-UHFFFAOYSA-N butane-1,4-diol Chemical compound OCCCCO WERYXYBDKMZEQL-UHFFFAOYSA-N 0.000 description 2
WQAQPCDUOCURKW-UHFFFAOYSA-N butanethiol Chemical compound CCCCS WQAQPCDUOCURKW-UHFFFAOYSA-N 0.000 description 2
CJZGTCYPCWQAJB-UHFFFAOYSA-L calcium stearate Chemical compound [Ca+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O CJZGTCYPCWQAJB-UHFFFAOYSA-L 0.000 description 2
239000008116 calcium stearate Substances 0.000 description 2
235000013539 calcium stearate Nutrition 0.000 description 2
239000003054 catalyst Substances 0.000 description 2
239000004927 clay Substances 0.000 description 2
RWGFKTVRMDUZSP-UHFFFAOYSA-N cumene Chemical compound CC(C)C1=CC=CC=C1 RWGFKTVRMDUZSP-UHFFFAOYSA-N 0.000 description 2
238000007865 diluting Methods 0.000 description 2
238000010438 heat treatment Methods 0.000 description 2
239000012442 inert solvent Substances 0.000 description 2
230000002401 inhibitory effect Effects 0.000 description 2
239000003999 initiator Substances 0.000 description 2
239000000976 ink Substances 0.000 description 2
NIMLQBUJDJZYEJ-UHFFFAOYSA-N isophorone diisocyanate Chemical compound CC1(C)CC(N=C=O)CC(C)(CN=C=O)C1 NIMLQBUJDJZYEJ-UHFFFAOYSA-N 0.000 description 2
QQVIHTHCMHWDBS-UHFFFAOYSA-N isophthalic acid Chemical compound OC(=O)C1=CC=CC(C(O)=O)=C1 QQVIHTHCMHWDBS-UHFFFAOYSA-N 0.000 description 2
239000004922 lacquer Substances 0.000 description 2
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150000002924 oxiranes Chemical class 0.000 description 2
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WXZMFSXDPGVJKK-UHFFFAOYSA-N pentaerythritol Chemical compound OCC(CO)(CO)CO WXZMFSXDPGVJKK-UHFFFAOYSA-N 0.000 description 2
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150000003141 primary amines Chemical class 0.000 description 2
239000000047 product Substances 0.000 description 2
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YTZKOQUCBOVLHL-UHFFFAOYSA-N tert-butylbenzene Chemical compound CC(C)(C)C1=CC=CC=C1 YTZKOQUCBOVLHL-UHFFFAOYSA-N 0.000 description 2
HJUGFYREWKUQJT-UHFFFAOYSA-N tetrabromomethane Chemical compound BrC(Br)(Br)Br HJUGFYREWKUQJT-UHFFFAOYSA-N 0.000 description 2
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XOOUIPVCVHRTMJ-UHFFFAOYSA-L zinc stearate Chemical compound [Zn+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O XOOUIPVCVHRTMJ-UHFFFAOYSA-L 0.000 description 2
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VYMPLPIFKRHAAC-UHFFFAOYSA-N 1,2-ethanedithiol Chemical compound SCCS VYMPLPIFKRHAAC-UHFFFAOYSA-N 0.000 description 1
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VGHSXKTVMPXHNG-UHFFFAOYSA-N 1,3-diisocyanatobenzene Chemical compound O=C=NC1=CC=CC(N=C=O)=C1 VGHSXKTVMPXHNG-UHFFFAOYSA-N 0.000 description 1
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MPPPKRYCTPRNTB-UHFFFAOYSA-N 1-bromobutane Chemical compound CCCCBr MPPPKRYCTPRNTB-UHFFFAOYSA-N 0.000 description 1
VFWCMGCRMGJXDK-UHFFFAOYSA-N 1-chlorobutane Chemical compound CCCCCl VFWCMGCRMGJXDK-UHFFFAOYSA-N 0.000 description 1
ICLCCFKUSALICQ-UHFFFAOYSA-N 1-isocyanato-4-(4-isocyanato-3-methylphenyl)-2-methylbenzene Chemical compound C1=C(N=C=O)C(C)=CC(C=2C=C(C)C(N=C=O)=CC=2)=C1 ICLCCFKUSALICQ-UHFFFAOYSA-N 0.000 description 1
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KSJBMDCFYZKAFH-UHFFFAOYSA-N 2-(2-sulfanylethylsulfanyl)ethanethiol Chemical compound SCCSCCS KSJBMDCFYZKAFH-UHFFFAOYSA-N 0.000 description 1
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HZAXFHJVJLSVMW-UHFFFAOYSA-N 2-Aminoethan-1-ol Chemical compound NCCO HZAXFHJVJLSVMW-UHFFFAOYSA-N 0.000 description 1
XHJGXOOOMKCJPP-UHFFFAOYSA-N 2-[tert-butyl(2-hydroxyethyl)amino]ethanol Chemical compound OCCN(C(C)(C)C)CCO XHJGXOOOMKCJPP-UHFFFAOYSA-N 0.000 description 1
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GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical compound CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 description 1
BLRPTPMANUNPDV-UHFFFAOYSA-N Silane Chemical compound [SiH4] BLRPTPMANUNPDV-UHFFFAOYSA-N 0.000 description 1
GSEJCLTVZPLZKY-UHFFFAOYSA-N Triethanolamine Chemical compound OCCN(CCO)CCO GSEJCLTVZPLZKY-UHFFFAOYSA-N 0.000 description 1
DAKWPKUUDNSNPN-UHFFFAOYSA-N Trimethylolpropane triacrylate Chemical compound C=CC(=O)OCC(CC)(COC(=O)C=C)COC(=O)C=C DAKWPKUUDNSNPN-UHFFFAOYSA-N 0.000 description 1
239000007983 Tris buffer Substances 0.000 description 1
229920001807 Urea-formaldehyde Polymers 0.000 description 1
RUDUCNPHDIMQCY-UHFFFAOYSA-N [3-(2-sulfanylacetyl)oxy-2,2-bis[(2-sulfanylacetyl)oxymethyl]propyl] 2-sulfanylacetate Chemical compound SCC(=O)OCC(COC(=O)CS)(COC(=O)CS)COC(=O)CS RUDUCNPHDIMQCY-UHFFFAOYSA-N 0.000 description 1
IYPNRTQAOXLCQW-UHFFFAOYSA-N [4-(sulfanylmethyl)phenyl]methanethiol Chemical compound SCC1=CC=C(CS)C=C1 IYPNRTQAOXLCQW-UHFFFAOYSA-N 0.000 description 1
IUHFWCGCSVTMPG-UHFFFAOYSA-N [C].[C] Chemical group [C].[C] IUHFWCGCSVTMPG-UHFFFAOYSA-N 0.000 description 1
238000005299 abrasion Methods 0.000 description 1
238000000862 absorption spectrum Methods 0.000 description 1
239000002253 acid Substances 0.000 description 1
150000001252 acrylic acid derivatives Chemical class 0.000 description 1
239000001361 adipic acid Substances 0.000 description 1
235000011037 adipic acid Nutrition 0.000 description 1
150000001299 aldehydes Chemical class 0.000 description 1
125000004183 alkoxy alkyl group Chemical group 0.000 description 1
229920000180 alkyd Polymers 0.000 description 1
125000002947 alkylene group Chemical group 0.000 description 1
CEGOLXSVJUTHNZ-UHFFFAOYSA-K aluminium tristearate Chemical compound [Al+3].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O CEGOLXSVJUTHNZ-UHFFFAOYSA-K 0.000 description 1
229940063655 aluminum stearate Drugs 0.000 description 1
150000001412 amines Chemical class 0.000 description 1
238000013459 approach Methods 0.000 description 1
150000003934 aromatic aldehydes Chemical class 0.000 description 1
150000008365 aromatic ketones Chemical class 0.000 description 1
125000000732 arylene group Chemical group 0.000 description 1
239000010425 asbestos Substances 0.000 description 1
ZWOASCVFHSYHOB-UHFFFAOYSA-N benzene-1,3-dithiol Chemical compound SC1=CC=CC(S)=C1 ZWOASCVFHSYHOB-UHFFFAOYSA-N 0.000 description 1
235000019400 benzoyl peroxide Nutrition 0.000 description 1
230000000903 blocking effect Effects 0.000 description 1
235000019437 butane-1,3-diol Nutrition 0.000 description 1
CQEYYJKEWSMYFG-UHFFFAOYSA-N butyl acrylate Chemical compound CCCCOC(=O)C=C CQEYYJKEWSMYFG-UHFFFAOYSA-N 0.000 description 1
KMGBZBJJOKUPIA-UHFFFAOYSA-N butyl iodide Chemical compound CCCCI KMGBZBJJOKUPIA-UHFFFAOYSA-N 0.000 description 1
238000004364 calculation method Methods 0.000 description 1
229910052799 carbon Inorganic materials 0.000 description 1
125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 1
238000001311 chemical methods and process Methods 0.000 description 1
239000007795 chemical reaction product Substances 0.000 description 1
229910052570 clay Inorganic materials 0.000 description 1
230000000052 comparative effect Effects 0.000 description 1
239000007859 condensation product Substances 0.000 description 1
230000001276 controlling effect Effects 0.000 description 1
238000004132 cross linking Methods 0.000 description 1
125000002993 cycloalkylene group Chemical group 0.000 description 1
QVTZUVMKKRFSCC-UHFFFAOYSA-N cyclohexanamine;methane Chemical compound C.NC1CCCCC1.NC1CCCCC1 QVTZUVMKKRFSCC-UHFFFAOYSA-N 0.000 description 1
KBLWLMPSVYBVDK-UHFFFAOYSA-N cyclohexyl prop-2-enoate Chemical compound C=CC(=O)OC1CCCCC1 KBLWLMPSVYBVDK-UHFFFAOYSA-N 0.000 description 1
PAFZNILMFXTMIY-UHFFFAOYSA-N cyclohexylamine Chemical compound NC1CCCCC1 PAFZNILMFXTMIY-UHFFFAOYSA-N 0.000 description 1
UFULAYFCSOUIOV-UHFFFAOYSA-N cysteamine Chemical compound NCCS UFULAYFCSOUIOV-UHFFFAOYSA-N 0.000 description 1
UOQACRNTVQWTFF-UHFFFAOYSA-N decane-1,10-dithiol Chemical compound SCCCCCCCCCCS UOQACRNTVQWTFF-UHFFFAOYSA-N 0.000 description 1
230000001627 detrimental effect Effects 0.000 description 1
238000011161 development Methods 0.000 description 1
235000014113 dietary fatty acids Nutrition 0.000 description 1
125000005442 diisocyanate group Chemical group 0.000 description 1
239000000539 dimer Substances 0.000 description 1
229910001882 dioxygen Inorganic materials 0.000 description 1
WNAHIZMDSQCWRP-UHFFFAOYSA-N dodecane-1-thiol Chemical compound CCCCCCCCCCCCS WNAHIZMDSQCWRP-UHFFFAOYSA-N 0.000 description 1
239000000975 dye Substances 0.000 description 1
230000000694 effects Effects 0.000 description 1
238000000295 emission spectrum Methods 0.000 description 1
238000005265 energy consumption Methods 0.000 description 1
239000004744 fabric Substances 0.000 description 1
239000000194 fatty acid Substances 0.000 description 1
229930195729 fatty acid Natural products 0.000 description 1
239000012467 final product Substances 0.000 description 1
230000005283 ground state Effects 0.000 description 1
125000001188 haloalkyl group Chemical group 0.000 description 1
230000005802 health problem Effects 0.000 description 1
RRAMGCGOFNQTLD-UHFFFAOYSA-N hexamethylene diisocyanate Chemical compound O=C=NCCCCCCN=C=O RRAMGCGOFNQTLD-UHFFFAOYSA-N 0.000 description 1
LNMQRPPRQDGUDR-UHFFFAOYSA-N hexyl prop-2-enoate Chemical compound CCCCCCOC(=O)C=C LNMQRPPRQDGUDR-UHFFFAOYSA-N 0.000 description 1
239000007970 homogeneous dispersion Substances 0.000 description 1
125000002768 hydroxyalkyl group Chemical group 0.000 description 1
238000011090 industrial biotechnology method and process Methods 0.000 description 1
239000011261 inert gas Substances 0.000 description 1
230000000977 initiatory effect Effects 0.000 description 1
230000001678 irradiating effect Effects 0.000 description 1
150000002576 ketones Chemical class 0.000 description 1
238000009533 lab test Methods 0.000 description 1
229940049918 linoleate Drugs 0.000 description 1
239000007788 liquid 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
CBBVHSHLSCZIHD-UHFFFAOYSA-N mercury silver Chemical compound [Ag].[Hg] CBBVHSHLSCZIHD-UHFFFAOYSA-N 0.000 description 1
229910052751 metal Inorganic materials 0.000 description 1
239000002184 metal Substances 0.000 description 1
150000002739 metals Chemical class 0.000 description 1
FQPSGWSUVKBHSU-UHFFFAOYSA-N methacrylamide Chemical compound CC(=C)C(N)=O FQPSGWSUVKBHSU-UHFFFAOYSA-N 0.000 description 1
YDKNBNOOCSNPNS-UHFFFAOYSA-N methyl 1,3-benzoxazole-2-carboxylate Chemical compound C1=CC=C2OC(C(=O)OC)=NC2=C1 YDKNBNOOCSNPNS-UHFFFAOYSA-N 0.000 description 1
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
238000002156 mixing Methods 0.000 description 1
MDYPDLBFDATSCF-UHFFFAOYSA-N nonyl prop-2-enoate Chemical compound CCCCCCCCCOC(=O)C=C MDYPDLBFDATSCF-UHFFFAOYSA-N 0.000 description 1
LZIMBRCILNYJOE-UHFFFAOYSA-N octane-1,6-dithiol Chemical compound CCC(S)CCCCCS LZIMBRCILNYJOE-UHFFFAOYSA-N 0.000 description 1
229940065472 octyl acrylate Drugs 0.000 description 1
ANISOHQJBAQUQP-UHFFFAOYSA-N octyl prop-2-enoate Chemical compound CCCCCCCCOC(=O)C=C ANISOHQJBAQUQP-UHFFFAOYSA-N 0.000 description 1
229940049964 oleate Drugs 0.000 description 1
125000000962 organic group Chemical group 0.000 description 1
NFHFRUOZVGFOOS-UHFFFAOYSA-N palladium;triphenylphosphane Chemical compound [Pd].C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1.C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1.C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1.C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1 NFHFRUOZVGFOOS-UHFFFAOYSA-N 0.000 description 1
125000005359 phenoxyalkyl group Chemical group 0.000 description 1
208000017983 photosensitivity disease Diseases 0.000 description 1
229920003023 plastic Polymers 0.000 description 1
239000004033 plastic Substances 0.000 description 1
229920000058 polyacrylate Polymers 0.000 description 1
229920001281 polyalkylene Polymers 0.000 description 1
229920006122 polyamide resin Polymers 0.000 description 1
229920000768 polyamine Polymers 0.000 description 1
229920001610 polycaprolactone Polymers 0.000 description 1
229920000728 polyester Polymers 0.000 description 1
229920005906 polyester polyol Polymers 0.000 description 1
229920000573 polyethylene Polymers 0.000 description 1
229920001223 polyethylene glycol Polymers 0.000 description 1
229920001296 polysiloxane Chemical class 0.000 description 1
239000004814 polyurethane Substances 0.000 description 1
229920002635 polyurethane Polymers 0.000 description 1
238000001556 precipitation Methods 0.000 description 1
239000002243 precursor Substances 0.000 description 1
239000010453 quartz Substances 0.000 description 1
229920013730 reactive polymer Polymers 0.000 description 1
229910052895 riebeckite Inorganic materials 0.000 description 1
150000003335 secondary amines Chemical class 0.000 description 1
238000000926 separation method Methods 0.000 description 1
229910000077 silane Inorganic materials 0.000 description 1
229920002545 silicone oil Polymers 0.000 description 1
235000012424 soybean oil Nutrition 0.000 description 1
239000003549 soybean oil Substances 0.000 description 1
125000001424 substituent group Chemical group 0.000 description 1
238000006467 substitution reaction Methods 0.000 description 1
150000005846 sugar alcohols Polymers 0.000 description 1
WMXCDAVJEZZYLT-UHFFFAOYSA-N tert-butylthiol Chemical compound CC(C)(C)S WMXCDAVJEZZYLT-UHFFFAOYSA-N 0.000 description 1
150000003510 tertiary aliphatic amines Chemical class 0.000 description 1
229920002803 thermoplastic polyurethane Polymers 0.000 description 1
229940071127 thioglycolate Drugs 0.000 description 1
CWERGRDVMFNCDR-UHFFFAOYSA-M thioglycolate(1-) Chemical compound [O-]C(=O)CS CWERGRDVMFNCDR-UHFFFAOYSA-M 0.000 description 1
150000003573 thiols Chemical class 0.000 description 1
RUELTTOHQODFPA-UHFFFAOYSA-N toluene 2,6-diisocyanate Chemical compound CC1=C(N=C=O)C=CC=C1N=C=O RUELTTOHQODFPA-UHFFFAOYSA-N 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
ZIBGPFATKBEMQZ-UHFFFAOYSA-N triethylene glycol Chemical compound OCCOCCOCCO ZIBGPFATKBEMQZ-UHFFFAOYSA-N 0.000 description 1
UFTFJSFQGQCHQW-UHFFFAOYSA-N triformin Chemical compound O=COCC(OC=O)COC=O UFTFJSFQGQCHQW-UHFFFAOYSA-N 0.000 description 1
229920006305 unsaturated polyester Polymers 0.000 description 1
JOYRKODLDBILNP-UHFFFAOYSA-N urethane group Chemical group NC(=O)OCC JOYRKODLDBILNP-UHFFFAOYSA-N 0.000 description 1
239000000080 wetting agent Substances 0.000 description 1
239000002023 wood Substances 0.000 description 1
229910052724 xenon Inorganic materials 0.000 description 1
FHNFHKCVQCLJFQ-UHFFFAOYSA-N xenon atom Chemical compound [Xe] FHNFHKCVQCLJFQ-UHFFFAOYSA-N 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
- B05D5/00—Processes for applying liquids or other fluent materials to surfaces to obtain special surface effects, finishes or structures
- B05D5/06—Processes for applying liquids or other fluent materials to surfaces to obtain special surface effects, finishes or structures to obtain multicolour or other optical effects
- B—PERFORMING OPERATIONS; TRANSPORTING
- B41—PRINTING; LINING MACHINES; TYPEWRITERS; STAMPS
- B41M—PRINTING, DUPLICATING, MARKING, OR COPYING PROCESSES; COLOUR PRINTING
- B41M7/00—After-treatment of prints, e.g. heating, irradiating, setting of the ink, protection of the printed stock
- B41M7/0045—After-treatment of prints, e.g. heating, irradiating, setting of the ink, protection of the printed stock using protective coatings or film forming compositions cured by mechanical wave energy, e.g. ultrasonics, cured by electromagnetic radiation or waves, e.g. ultraviolet radiation, electron beams, or cured by magnetic or electric fields, e.g. electric discharge, plasma
- B—PERFORMING OPERATIONS; TRANSPORTING
- B41—PRINTING; LINING MACHINES; TYPEWRITERS; STAMPS
- B41M—PRINTING, DUPLICATING, MARKING, OR COPYING PROCESSES; COLOUR PRINTING
- B41M7/00—After-treatment of prints, e.g. heating, irradiating, setting of the ink, protection of the printed stock
- B41M7/0081—After-treatment of prints, e.g. heating, irradiating, setting of the ink, protection of the printed stock using electromagnetic radiation or waves, e.g. ultraviolet radiation, electron beams

Landscapes

Electromagnetism (AREA)
Physics & Mathematics (AREA)
General Health & Medical Sciences (AREA)
Mechanical Engineering (AREA)
Plasma & Fusion (AREA)
Health & Medical Sciences (AREA)
Engineering & Computer Science (AREA)
Toxicology (AREA)
Paints Or Removers (AREA)
Polymerisation Methods In General (AREA)
Inks, Pencil-Leads, Or Crayons (AREA)
Laminated Bodies (AREA)
Macromonomer-Based Addition Polymer (AREA)
Application Of Or Painting With Fluid Materials (AREA)

NO792123A 1978-06-26 1979-06-25 Herdbare sammensetninger for oppnaaelse av overflater med lav glans NO792123L (no)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
US05/918,983 US4169167A (en)	1978-06-26	1978-06-26	Low gloss finishes by gradient intensity cure

Publications (1)

Publication Number	Publication Date
NO792123L true NO792123L (no)	1979-12-28

Family

ID=25441277

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
NO792123A NO792123L (no)	1978-06-26	1979-06-25	Herdbare sammensetninger for oppnaaelse av overflater med lav glans

Country Status (12)

Country	Link
US (1)	US4169167A (fr)
JP (1)	JPS555997A (fr)
AU (1)	AU531143B2 (fr)
BE (1)	BE877230A (fr)
CA (1)	CA1120631A (fr)
DE (1)	DE2925180A1 (fr)
FR (1)	FR2429818A1 (fr)
GB (1)	GB2025993B (fr)
NL (1)	NL7904977A (fr)
NO (1)	NO792123L (fr)
SE (1)	SE7905526L (fr)
ZA (1)	ZA792779B (fr)

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EP0007468B1 (fr) *	1978-07-13	1982-04-07	Ciba-Geigy Ag	Photocurable compositions
US4313969A (en) *	1979-09-10	1982-02-02	Fusion Systems Corporation	Method and apparatus for providing low gloss and gloss controlled radiation-cured coatings
US4391686A (en) *	1980-08-25	1983-07-05	Lord Corporation	Actinic radiation curable formulations
US4514271A (en) *	1981-07-02	1985-04-30	Gaf Corporation	Stable dispersion of alkylated polyvinylpyrrolidone and vinyl pyrrolidone
US4417023A (en) *	1982-01-21	1983-11-22	Diamond Shamrock Corporation	Polysiloxane stabilizers for flatting agents in radiation hardenable compositions
US4421784A (en) *	1982-02-12	1983-12-20	Union Carbide Corporation	Process for producing textured coatings
US4526913A (en) *	1984-01-13	1985-07-02	J. H. Diamond Company	Dimer polymeric coating selectively strippable as cohesive film
US6376569B1 (en) *	1990-12-13	2002-04-23	3M Innovative Properties Company	Hydrosilation reaction utilizing a (cyclopentadiene)(sigma-aliphatic) platinum complex and a free radical photoinitiator
US6046250A (en) *	1990-12-13	2000-04-04	3M Innovative Properties Company	Hydrosilation reaction utilizing a free radical photoinitiator
KR20000005437A (ko) *	1996-04-10	2000-01-25	덴 아르토그 제로엔 헨드리쿠스 조셉	방사-경화된 내부 일차코팅재와 광학 유리섬유사이의 부착력을향상시키는 방법
TW448236B (en) *	1996-05-21	2001-08-01	Matsushita Electric Industrial Co Ltd	Thin film, method and apparatus for forming the same, and electronic component incorporating the same
ATE279487T1 (de)	1999-07-28	2004-10-15	Armstrong World Ind Inc	Zusammensetzung und verfahren für eine glanzkontrollierte, abreibwiderstandsfeste beschichtung auf produktoberflächen
US6333076B1 (en)	1999-07-28	2001-12-25	Armstrong World Industries, Inc.	Composition and method for manufacturing a surface covering product having a controlled gloss surface coated wearlayer
US6399670B1 (en)	2000-01-21	2002-06-04	Congoleum Corporation	Coating having macroscopic texture and process for making same
US6461689B1 (en)	2000-08-31	2002-10-08	Domco Tarkett Inc.	Method of controlling specular gloss characteristics
US6426034B1 (en) *	2000-10-31	2002-07-30	Lilly Industries, Inc.	Radiation curable coating for thermoplastic substrates
US6908663B1 (en)	2000-11-15	2005-06-21	Awi Licensing Company	Pigmented radiation cured wear layer
DE10100170A1 (de) *	2001-01-04	2002-07-11	Basf Ag	Beschichtungsmittel
US6890625B2 (en) *	2001-02-05	2005-05-10	Awi Licensing Company	Surface covering having gloss in-register and method of making
US6759096B2 (en)	2001-09-24	2004-07-06	Congoleum Corporation	Method for making differential gloss coverings
GB2448695B (en) *	2007-04-23	2012-07-11	Inca Digital Printers Ltd	Large-scale inkjet printer
US7985472B2 (en) *	2007-06-22	2011-07-26	Exopack-Technology, Llc	Low-gloss dry-erase coating formulation
US9139742B2 (en) *	2007-07-12	2015-09-22	Coveris Technology Llc	Low-gloss anti-graffiti surface for electronic white boards
US20090162538A1 (en) *	2007-12-20	2009-06-25	Frank-Rainer Boehm	Composition for fixing wound items
US8105659B2 (en) *	2008-07-11	2012-01-31	Xerox Corporation	Method of controlling gloss with curing atmosphere using radiation curable ink or overcoat compositions
CN102107340B (zh) *	2009-12-24	2015-10-21	汉高股份有限及两合公司	一种焊膏组合物、焊膏及一种助焊剂
US20120015110A1 (en) *	2010-07-19	2012-01-19	Dong Tian	Ultraviolet curable coating
US8906468B2 (en) *	2011-10-27	2014-12-09	Ppg Industries Ohio, Inc.	Low gloss UV-cured coatings for aircraft
US11745475B2 (en)	2016-08-19	2023-09-05	Wilsonart Llc	Surfacing materials and method of manufacture
US11077639B2 (en)	2016-08-19	2021-08-03	Wilsonart Llc	Surfacing materials and method of manufacture
US11504955B2 (en)	2016-08-19	2022-11-22	Wilsonart Llc	Decorative laminate with matte finish and method of manufacture
US10933608B2 (en) *	2016-08-19	2021-03-02	Wilsonart Llc	Surfacing materials and method of manufacture
KR102216826B1 (ko) *	2017-05-22	2021-02-18	(주)엘지하우시스	내오염성이 우수한 저광택 경화물 및 이의 제조방법
PL4423155T3 (pl) *	2021-10-29	2025-12-08	Covestro (Netherlands) B.V.	Kompozycja utwardzalna rodnikowo

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GB1115813A (en) *	1965-06-01	1968-05-29	Agfa Gevaert Nv	Method for recording and reproducing information by surface modification of a polymeric composition
GB1141544A (en) *	1966-07-13	1969-01-29	Gordon Owen Shipton	Polymer compositions
US3759807A (en) *	1969-01-28	1973-09-18	Union Carbide Corp	Photopolymerization process using combination of organic carbonyls and amines
US3850675A (en) *	1970-11-30	1974-11-26	Weyerhaeuser Co	Use of ultraviolet light to cure uncured surface layer resulting from air inhibition in preceding high energy ionizing radiation curing process
US3759808A (en) *	1971-04-20	1973-09-18	Ppg Industries Inc	Unsaturated diacrylates polymerized with ultraviolet light
US4020193A (en) *	1971-04-20	1977-04-26	Ppg Industries, Inc.	Method of forming a non-glossy film
US3953622A (en) *	1971-04-20	1976-04-27	Ppg Industries, Inc.	Method of forming a non-glossy film
US3918393A (en) *	1971-09-10	1975-11-11	Ppg Industries Inc	Method of producing flat (non-glossy) films
US3783004A (en) *	1971-09-21	1974-01-01	Ppg Industries Inc	Method of forming a flat coated surface
US3943046A (en) *	1973-06-25	1976-03-09	Scm Corporation	UV curing process employing flash photolysis
DE2442879C3 (de) *	1973-09-17	1978-12-14	Nippon Paint Co., Ltd., Osaka (Japan)	Verfahren zum Härten von lichthärtbaren Anstrichmitteln und Überzugsmassen
GB1509312A (en) *	1974-04-01	1978-05-04	Nippon Paint Co Ltd	Method and apparatus for curing photo-curable composition
US4017652A (en) *	1974-10-23	1977-04-12	Ppg Industries, Inc.	Photocatalyst system and ultraviolet light curable coating compositions containing the same
US4048036A (en) *	1974-10-24	1977-09-13	Ppg Industries, Inc.	Process for producing films of low gloss by exposure to ultraviolet light
US3992275A (en) *	1974-11-25	1976-11-16	Celanese Corporation	Low gloss ultraviolet curable coatings utilizing α,α,α-trichlorotoluene as a photoinitiator
US3966572A (en) *	1975-02-11	1976-06-29	Union Carbide Corporation	Photocurable low gloss coatings containing silica and acrylic acid
US4075366A (en) *	1976-06-11	1978-02-21	Desoto, Inc.	Low gloss radiation cure

1978
- 1978-06-26 US US05/918,983 patent/US4169167A/en not_active Expired - Lifetime
1979
- 1979-06-05 ZA ZA792779A patent/ZA792779B/xx unknown
- 1979-06-14 CA CA000329801A patent/CA1120631A/fr not_active Expired
- 1979-06-21 AU AU48276/79A patent/AU531143B2/en not_active Ceased
- 1979-06-22 DE DE19792925180 patent/DE2925180A1/de not_active Withdrawn
- 1979-06-25 FR FR7916244A patent/FR2429818A1/fr not_active Withdrawn
- 1979-06-25 JP JP8007179A patent/JPS555997A/ja active Pending
- 1979-06-25 SE SE7905526A patent/SE7905526L/xx not_active Application Discontinuation
- 1979-06-25 NO NO792123A patent/NO792123L/no unknown
- 1979-06-25 BE BE0/195932A patent/BE877230A/fr not_active IP Right Cessation
- 1979-06-26 NL NL7904977A patent/NL7904977A/xx not_active Application Discontinuation
- 1979-06-26 GB GB7922174A patent/GB2025993B/en not_active Expired

Also Published As

Publication number	Publication date
NL7904977A (nl)	1979-12-28
GB2025993A (en)	1980-01-30
US4169167A (en)	1979-09-25
JPS555997A (en)	1980-01-17
AU4827679A (en)	1980-01-03
BE877230A (fr)	1979-12-27
DE2925180A1 (de)	1980-01-10
GB2025993B (en)	1982-11-03
ZA792779B (en)	1980-11-26
CA1120631A (fr)	1982-03-23
SE7905526L (sv)	1979-12-27
FR2429818A1 (fr)	1980-01-25
AU531143B2 (en)	1983-08-11

Publication	Publication Date	Title
NO792123L (no)	1979-12-28	Herdbare sammensetninger for oppnaaelse av overflater med lav glans
US4174307A (en)	1979-11-13	Room-temperature-radiation-curable polyurethane
US4358476A (en)	1982-11-09	Radiation-curable compositions containing water
US5629359A (en)	1997-05-13	Radiation curable compositions
US4133723A (en)	1979-01-09	Actinic radiation-curable formulations from the reaction product of organic isocyanate, poly(alkylene oxide) polyol and an unsaturated addition-polymerizable monomeric compound having a single isocyanate-reactive hydrogen group
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