FI57436C - Anvaendning av en pao akrylharts baserad belaeggning foer utbelaeggning av ett polykarbonatsubstrat - Google Patents
Anvaendning av en pao akrylharts baserad belaeggning foer utbelaeggning av ett polykarbonatsubstrat Download PDFInfo
- Publication number
- FI57436C FI57436C FI1221/73A FI122173A FI57436C FI 57436 C FI57436 C FI 57436C FI 1221/73 A FI1221/73 A FI 1221/73A FI 122173 A FI122173 A FI 122173A FI 57436 C FI57436 C FI 57436C
- Authority
- FI
- Finland
- Prior art keywords
- weight
- coating
- hydroxy
- polycarbonate
- acid
- Prior art date
Links
- 238000000576 coating method Methods 0.000 claims description 48
- 239000011248 coating agent Substances 0.000 claims description 41
- 229920000515 polycarbonate Polymers 0.000 claims description 33
- 239000004417 polycarbonate Substances 0.000 claims description 33
- -1 hydroxyalkyl ester Chemical class 0.000 claims description 25
- 239000004925 Acrylic resin Substances 0.000 claims description 21
- 229920000178 Acrylic resin Polymers 0.000 claims description 21
- 229920000728 polyester Polymers 0.000 claims description 15
- 150000001732 carboxylic acid derivatives Chemical class 0.000 claims description 10
- 150000002009 diols Chemical class 0.000 claims description 8
- BNCADMBVWNPPIZ-UHFFFAOYSA-N 2-n,2-n,4-n,4-n,6-n,6-n-hexakis(methoxymethyl)-1,3,5-triazine-2,4,6-triamine Chemical group COCN(COC)C1=NC(N(COC)COC)=NC(N(COC)COC)=N1 BNCADMBVWNPPIZ-UHFFFAOYSA-N 0.000 claims description 7
- 150000001412 amines Chemical class 0.000 claims description 7
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 claims description 6
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 claims description 6
- 239000000758 substrate Substances 0.000 claims description 6
- RCHKEJKUUXXBSM-UHFFFAOYSA-N n-benzyl-2-(3-formylindol-1-yl)acetamide Chemical compound C12=CC=CC=C2C(C=O)=CN1CC(=O)NCC1=CC=CC=C1 RCHKEJKUUXXBSM-UHFFFAOYSA-N 0.000 claims description 5
- 229920005989 resin Polymers 0.000 claims description 5
- 239000011347 resin Substances 0.000 claims description 5
- JIGUQPWFLRLWPJ-UHFFFAOYSA-N Ethyl acrylate Chemical compound CCOC(=O)C=C JIGUQPWFLRLWPJ-UHFFFAOYSA-N 0.000 claims description 4
- VVQNEPGJFQJSBK-UHFFFAOYSA-N Methyl methacrylate Chemical compound COC(=O)C(C)=C VVQNEPGJFQJSBK-UHFFFAOYSA-N 0.000 claims description 4
- 239000003431 cross linking reagent Substances 0.000 claims description 4
- PNJWIWWMYCMZRO-UHFFFAOYSA-N pent‐4‐en‐2‐one Natural products CC(=O)CC=C PNJWIWWMYCMZRO-UHFFFAOYSA-N 0.000 claims description 4
- 229920001610 polycaprolactone Polymers 0.000 claims description 4
- 239000004632 polycaprolactone Substances 0.000 claims description 4
- 125000005907 alkyl ester group Chemical group 0.000 claims description 3
- GNSFRPWPOGYVLO-UHFFFAOYSA-N 3-hydroxypropyl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OCCCO GNSFRPWPOGYVLO-UHFFFAOYSA-N 0.000 claims description 2
- 238000012360 testing method Methods 0.000 description 26
- 239000000203 mixture Substances 0.000 description 25
- 239000002904 solvent Substances 0.000 description 22
- 239000008199 coating composition Substances 0.000 description 21
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 18
- 239000000126 substance Substances 0.000 description 16
- 239000002253 acid Substances 0.000 description 13
- MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical class OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 13
- 239000000463 material Substances 0.000 description 13
- JOXIMZWYDAKGHI-UHFFFAOYSA-N toluene-4-sulfonic acid Chemical compound CC1=CC=C(S(O)(=O)=O)C=C1 JOXIMZWYDAKGHI-UHFFFAOYSA-N 0.000 description 12
- LYCAIKOWRPUZTN-UHFFFAOYSA-N ethylene glycol Natural products OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 11
- 238000002474 experimental method Methods 0.000 description 11
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 10
- ZNQVEEAIQZEUHB-UHFFFAOYSA-N 2-ethoxyethanol Chemical compound CCOCCO ZNQVEEAIQZEUHB-UHFFFAOYSA-N 0.000 description 9
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 8
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical class OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 8
- 230000000052 comparative effect Effects 0.000 description 8
- 238000000034 method Methods 0.000 description 8
- 239000004342 Benzoyl peroxide Substances 0.000 description 7
- OMPJBNCRMGITSC-UHFFFAOYSA-N Benzoylperoxide Chemical compound C=1C=CC=CC=1C(=O)OOC(=O)C1=CC=CC=C1 OMPJBNCRMGITSC-UHFFFAOYSA-N 0.000 description 7
- 150000007513 acids Chemical class 0.000 description 7
- 235000019400 benzoyl peroxide Nutrition 0.000 description 7
- 239000003054 catalyst Substances 0.000 description 7
- 229920001577 copolymer Polymers 0.000 description 7
- 239000000178 monomer Substances 0.000 description 7
- 229920001187 thermosetting polymer Polymers 0.000 description 7
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 6
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 6
- 238000005299 abrasion Methods 0.000 description 6
- RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Substances CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 6
- 230000002378 acidificating effect Effects 0.000 description 5
- 125000004432 carbon atom Chemical group C* 0.000 description 5
- 150000001875 compounds Chemical class 0.000 description 5
- 150000002596 lactones Chemical class 0.000 description 5
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 4
- AMQJEAYHLZJPGS-UHFFFAOYSA-N N-Pentanol Chemical compound CCCCCO AMQJEAYHLZJPGS-UHFFFAOYSA-N 0.000 description 4
- 239000012963 UV stabilizer Substances 0.000 description 4
- 150000001299 aldehydes Chemical class 0.000 description 4
- 238000006243 chemical reaction Methods 0.000 description 4
- 239000007859 condensation product Substances 0.000 description 4
- 150000002148 esters Chemical class 0.000 description 4
- ZSIAUFGUXNUGDI-UHFFFAOYSA-N hexan-1-ol Chemical compound CCCCCCO ZSIAUFGUXNUGDI-UHFFFAOYSA-N 0.000 description 4
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 4
- 229920005862 polyol Polymers 0.000 description 4
- 150000003077 polyols Chemical class 0.000 description 4
- 229920001169 thermoplastic Polymers 0.000 description 4
- 239000004416 thermosoftening plastic Substances 0.000 description 4
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 3
- XNWFRZJHXBZDAG-UHFFFAOYSA-N 2-METHOXYETHANOL Chemical compound COCCO XNWFRZJHXBZDAG-UHFFFAOYSA-N 0.000 description 3
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 3
- WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 description 3
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
- WVDDGKGOMKODPV-UHFFFAOYSA-N Benzyl alcohol Chemical compound OCC1=CC=CC=C1 WVDDGKGOMKODPV-UHFFFAOYSA-N 0.000 description 3
- DKPFZGUDAPQIHT-UHFFFAOYSA-N Butyl acetate Natural products CCCCOC(C)=O DKPFZGUDAPQIHT-UHFFFAOYSA-N 0.000 description 3
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 3
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 3
- OFOBLEOULBTSOW-UHFFFAOYSA-N Malonic acid Chemical class OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 3
- 229920000877 Melamine resin Polymers 0.000 description 3
- 229910019142 PO4 Inorganic materials 0.000 description 3
- 150000001298 alcohols Chemical class 0.000 description 3
- 150000008064 anhydrides Chemical class 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 3
- FUZZWVXGSFPDMH-UHFFFAOYSA-N hexanoic acid Chemical compound CCCCCC(O)=O FUZZWVXGSFPDMH-UHFFFAOYSA-N 0.000 description 3
- 230000007062 hydrolysis Effects 0.000 description 3
- 238000006460 hydrolysis reaction Methods 0.000 description 3
- JDSHMPZPIAZGSV-UHFFFAOYSA-N melamine Chemical compound NC1=NC(N)=NC(N)=N1 JDSHMPZPIAZGSV-UHFFFAOYSA-N 0.000 description 3
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 3
- 229910052757 nitrogen Inorganic materials 0.000 description 3
- 235000021317 phosphate Nutrition 0.000 description 3
- 239000000049 pigment Substances 0.000 description 3
- 229920006289 polycarbonate film Polymers 0.000 description 3
- 229920000642 polymer Polymers 0.000 description 3
- 229920001296 polysiloxane Polymers 0.000 description 3
- BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 description 3
- CXWXQJXEFPUFDZ-UHFFFAOYSA-N tetralin Chemical compound C1=CC=C2CCCCC2=C1 CXWXQJXEFPUFDZ-UHFFFAOYSA-N 0.000 description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 3
- WSLDOOZREJYCGB-UHFFFAOYSA-N 1,2-Dichloroethane Chemical compound ClCCCl WSLDOOZREJYCGB-UHFFFAOYSA-N 0.000 description 2
- RFFLAFLAYFXFSW-UHFFFAOYSA-N 1,2-dichlorobenzene Chemical compound ClC1=CC=CC=C1Cl RFFLAFLAYFXFSW-UHFFFAOYSA-N 0.000 description 2
- RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 description 2
- BBMCTIGTTCKYKF-UHFFFAOYSA-N 1-heptanol Chemical compound CCCCCCCO BBMCTIGTTCKYKF-UHFFFAOYSA-N 0.000 description 2
- HGINCPLSRVDWNT-UHFFFAOYSA-N Acrolein Chemical compound C=CC=O HGINCPLSRVDWNT-UHFFFAOYSA-N 0.000 description 2
- NCOPIVIKUHWVDV-UHFFFAOYSA-N COC1(C(OC)=CC(C(C(C=CC=C2)=C2O)=O)=CC1)OC Chemical compound COC1(C(OC)=CC(C(C(C=CC=C2)=C2O)=O)=CC1)OC NCOPIVIKUHWVDV-UHFFFAOYSA-N 0.000 description 2
- LCGLNKUTAGEVQW-UHFFFAOYSA-N Dimethyl ether Chemical compound COC LCGLNKUTAGEVQW-UHFFFAOYSA-N 0.000 description 2
- YNQLUTRBYVCPMQ-UHFFFAOYSA-N Ethylbenzene Chemical compound CCC1=CC=CC=C1 YNQLUTRBYVCPMQ-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
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 2
- WVRPFQGZHKZCEB-UHFFFAOYSA-N Isopropyl 2-methylpropanoate Chemical compound CC(C)OC(=O)C(C)C WVRPFQGZHKZCEB-UHFFFAOYSA-N 0.000 description 2
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 description 2
- IMNFDUFMRHMDMM-UHFFFAOYSA-N N-Heptane Chemical compound CCCCCCC IMNFDUFMRHMDMM-UHFFFAOYSA-N 0.000 description 2
- OFBQJSOFQDEBGM-UHFFFAOYSA-N Pentane Chemical compound CCCCC OFBQJSOFQDEBGM-UHFFFAOYSA-N 0.000 description 2
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 2
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 2
- 239000006096 absorbing agent Substances 0.000 description 2
- 239000003377 acid catalyst Substances 0.000 description 2
- 230000002411 adverse Effects 0.000 description 2
- 229920000180 alkyd Polymers 0.000 description 2
- 125000005250 alkyl acrylate group Chemical group 0.000 description 2
- 125000000217 alkyl group Chemical group 0.000 description 2
- 150000004945 aromatic hydrocarbons Chemical class 0.000 description 2
- HUMNYLRZRPPJDN-UHFFFAOYSA-N benzaldehyde Chemical compound O=CC1=CC=CC=C1 HUMNYLRZRPPJDN-UHFFFAOYSA-N 0.000 description 2
- 239000012964 benzotriazole Substances 0.000 description 2
- BTANRVKWQNVYAZ-UHFFFAOYSA-N butan-2-ol Chemical compound CCC(C)O BTANRVKWQNVYAZ-UHFFFAOYSA-N 0.000 description 2
- 238000009833 condensation Methods 0.000 description 2
- 230000005494 condensation Effects 0.000 description 2
- 238000001816 cooling Methods 0.000 description 2
- 238000005336 cracking Methods 0.000 description 2
- HPXRVTGHNJAIIH-UHFFFAOYSA-N cyclohexanol Chemical compound OC1CCCCC1 HPXRVTGHNJAIIH-UHFFFAOYSA-N 0.000 description 2
- BGTOWKSIORTVQH-UHFFFAOYSA-N cyclopentanone Chemical compound O=C1CCCC1 BGTOWKSIORTVQH-UHFFFAOYSA-N 0.000 description 2
- 230000001627 detrimental effect Effects 0.000 description 2
- SWXVUIWOUIDPGS-UHFFFAOYSA-N diacetone alcohol Chemical compound CC(=O)CC(C)(C)O SWXVUIWOUIDPGS-UHFFFAOYSA-N 0.000 description 2
- DOIRQSBPFJWKBE-UHFFFAOYSA-N dibutyl phthalate Chemical compound CCCCOC(=O)C1=CC=CC=C1C(=O)OCCCC DOIRQSBPFJWKBE-UHFFFAOYSA-N 0.000 description 2
- HYBBIBNJHNGZAN-UHFFFAOYSA-N furfural Chemical compound O=CC1=CC=CO1 HYBBIBNJHNGZAN-UHFFFAOYSA-N 0.000 description 2
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 2
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 2
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 2
- 239000003999 initiator Substances 0.000 description 2
- HJOVHMDZYOCNQW-UHFFFAOYSA-N isophorone Chemical compound CC1=CC(=O)CC(C)(C)C1 HJOVHMDZYOCNQW-UHFFFAOYSA-N 0.000 description 2
- 229940024423 isopropyl isobutyrate Drugs 0.000 description 2
- 150000002576 ketones Chemical class 0.000 description 2
- XMGQYMWWDOXHJM-UHFFFAOYSA-N limonene Chemical compound CC(=C)C1CCC(C)=CC1 XMGQYMWWDOXHJM-UHFFFAOYSA-N 0.000 description 2
- 239000000314 lubricant Substances 0.000 description 2
- BJEPYKJPYRNKOW-UHFFFAOYSA-N malic acid Chemical compound OC(=O)C(O)CC(O)=O BJEPYKJPYRNKOW-UHFFFAOYSA-N 0.000 description 2
- 150000002734 metacrylic acid derivatives Chemical class 0.000 description 2
- UAEPNZWRGJTJPN-UHFFFAOYSA-N methylcyclohexane Chemical compound CC1CCCCC1 UAEPNZWRGJTJPN-UHFFFAOYSA-N 0.000 description 2
- 238000002156 mixing Methods 0.000 description 2
- XNLICIUVMPYHGG-UHFFFAOYSA-N pentan-2-one Chemical compound CCCC(C)=O XNLICIUVMPYHGG-UHFFFAOYSA-N 0.000 description 2
- FDPIMTJIUBPUKL-UHFFFAOYSA-N pentan-3-one Chemical compound CCC(=O)CC FDPIMTJIUBPUKL-UHFFFAOYSA-N 0.000 description 2
- 229920000058 polyacrylate Polymers 0.000 description 2
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 2
- 239000011541 reaction mixture Substances 0.000 description 2
- 230000003678 scratch resistant effect Effects 0.000 description 2
- 238000006748 scratching Methods 0.000 description 2
- 230000002393 scratching effect Effects 0.000 description 2
- 239000011877 solvent mixture Substances 0.000 description 2
- 238000003756 stirring Methods 0.000 description 2
- 238000010998 test method Methods 0.000 description 2
- VZGDMQKNWNREIO-UHFFFAOYSA-N tetrachloromethane Chemical compound ClC(Cl)(Cl)Cl VZGDMQKNWNREIO-UHFFFAOYSA-N 0.000 description 2
- NKKYDWOROGFFQP-UHFFFAOYSA-N (2,4-dibromophenyl)-(2-hydroxy-4-propoxyphenyl)methanone Chemical compound OC1=CC(OCCC)=CC=C1C(=O)C1=CC=C(Br)C=C1Br NKKYDWOROGFFQP-UHFFFAOYSA-N 0.000 description 1
- FUMDYLHISKQVPA-UHFFFAOYSA-N (2,4-dibutylphenyl)-(4-ethoxy-2-hydroxyphenyl)methanone Chemical compound CCCCC1=CC(CCCC)=CC=C1C(=O)C1=CC=C(OCC)C=C1O FUMDYLHISKQVPA-UHFFFAOYSA-N 0.000 description 1
- MYVOYWPHADXFTE-UHFFFAOYSA-N (2,4-dichlorophenyl)-(2-hydroxy-4-propoxyphenyl)methanone Chemical compound OC1=CC(OCCC)=CC=C1C(=O)C1=CC=C(Cl)C=C1Cl MYVOYWPHADXFTE-UHFFFAOYSA-N 0.000 description 1
- HKCCRRDTILVMHH-UHFFFAOYSA-N (2-chlorophenyl)-(2-hydroxy-4-methoxyphenyl)methanone Chemical compound OC1=CC(OC)=CC=C1C(=O)C1=CC=CC=C1Cl HKCCRRDTILVMHH-UHFFFAOYSA-N 0.000 description 1
- JNCAMJDQLFGUFU-UHFFFAOYSA-N (2-hydroxy-4-methoxy-3-methylphenyl)-(4-methoxyphenyl)methanone Chemical compound C1=CC(OC)=CC=C1C(=O)C1=CC=C(OC)C(C)=C1O JNCAMJDQLFGUFU-UHFFFAOYSA-N 0.000 description 1
- GXJIHRIICFQTSB-UHFFFAOYSA-N (2-hydroxy-4-methoxyphenyl)-(2-hydroxy-4-propoxyphenyl)methanone Chemical compound OC1=CC(OCCC)=CC=C1C(=O)C1=CC=C(OC)C=C1O GXJIHRIICFQTSB-UHFFFAOYSA-N 0.000 description 1
- BDACRXKSBPLSJG-UHFFFAOYSA-N (2-hydroxy-4-methoxyphenyl)-(4-methoxyphenyl)methanone Chemical compound C1=CC(OC)=CC=C1C(=O)C1=CC=C(OC)C=C1O BDACRXKSBPLSJG-UHFFFAOYSA-N 0.000 description 1
- QLUYTKYSRNDBJQ-UHFFFAOYSA-N (2-hydroxy-4-methoxyphenyl)-(4-propylphenyl)methanone Chemical compound C1=CC(CCC)=CC=C1C(=O)C1=CC=C(OC)C=C1O QLUYTKYSRNDBJQ-UHFFFAOYSA-N 0.000 description 1
- NNUNDQZDGVWLPX-UHFFFAOYSA-N (2-hydroxy-4-propoxyphenyl)-phenylmethanone Chemical compound OC1=CC(OCCC)=CC=C1C(=O)C1=CC=CC=C1 NNUNDQZDGVWLPX-UHFFFAOYSA-N 0.000 description 1
- DBMFEKRVYKRCOX-UHFFFAOYSA-N (4-bromophenyl)-(2-hydroxy-4-methoxyphenyl)methanone Chemical compound OC1=CC(OC)=CC=C1C(=O)C1=CC=C(Br)C=C1 DBMFEKRVYKRCOX-UHFFFAOYSA-N 0.000 description 1
- MFNFLYORYLEDCC-UHFFFAOYSA-N (4-bromophenyl)-(4-ethoxy-2-hydroxyphenyl)methanone Chemical compound OC1=CC(OCC)=CC=C1C(=O)C1=CC=C(Br)C=C1 MFNFLYORYLEDCC-UHFFFAOYSA-N 0.000 description 1
- ZLTOEPVLDMXKSX-UHFFFAOYSA-N (4-butoxy-2-hydroxyphenyl)-(2-hydroxy-4-methoxyphenyl)methanone Chemical compound OC1=CC(OCCCC)=CC=C1C(=O)C1=CC=C(OC)C=C1O ZLTOEPVLDMXKSX-UHFFFAOYSA-N 0.000 description 1
- GZNPRKADPXWQEA-UHFFFAOYSA-N (4-butoxy-2-hydroxyphenyl)-(3,4-dimethoxyphenyl)methanone Chemical compound OC1=CC(OCCCC)=CC=C1C(=O)C1=CC=C(OC)C(OC)=C1 GZNPRKADPXWQEA-UHFFFAOYSA-N 0.000 description 1
- GOTHWXZVXZVLEE-UHFFFAOYSA-N (4-butoxy-2-hydroxyphenyl)-(4-ethoxy-2-hydroxyphenyl)methanone Chemical compound OC1=CC(OCCCC)=CC=C1C(=O)C1=CC=C(OCC)C=C1O GOTHWXZVXZVLEE-UHFFFAOYSA-N 0.000 description 1
- IADJBCIKCXGXDN-UHFFFAOYSA-N (4-butoxy-2-hydroxyphenyl)-phenylmethanone Chemical compound OC1=CC(OCCCC)=CC=C1C(=O)C1=CC=CC=C1 IADJBCIKCXGXDN-UHFFFAOYSA-N 0.000 description 1
- ZSGNFDSWUMYCJP-UHFFFAOYSA-N (4-butoxy-3-hydroxyphenyl)-(2-hydroxy-4-methoxyphenyl)methanone Chemical compound C1=C(O)C(OCCCC)=CC=C1C(=O)C1=CC=C(OC)C=C1O ZSGNFDSWUMYCJP-UHFFFAOYSA-N 0.000 description 1
- GGDMPTHZPYJRHD-UHFFFAOYSA-N (4-butylphenyl)-(4-ethoxy-2-hydroxyphenyl)methanone Chemical compound C1=CC(CCCC)=CC=C1C(=O)C1=CC=C(OCC)C=C1O GGDMPTHZPYJRHD-UHFFFAOYSA-N 0.000 description 1
- CBKGNZGFDXQOEV-UHFFFAOYSA-N (4-chlorophenyl)-(2-hydroxy-4-methoxyphenyl)methanone Chemical compound OC1=CC(OC)=CC=C1C(=O)C1=CC=C(Cl)C=C1 CBKGNZGFDXQOEV-UHFFFAOYSA-N 0.000 description 1
- GQQXBXFGGUSWNU-UHFFFAOYSA-N (4-chlorophenyl)-(4-ethoxy-2-hydroxyphenyl)methanone Chemical compound OC1=CC(OCC)=CC=C1C(=O)C1=CC=C(Cl)C=C1 GQQXBXFGGUSWNU-UHFFFAOYSA-N 0.000 description 1
- JFGFBYSYQKAFJF-UHFFFAOYSA-N (4-ethoxy-2-hydroxyphenyl)-(2-hydroxy-4-propoxyphenyl)methanone Chemical compound OC1=CC(OCCC)=CC=C1C(=O)C1=CC=C(OCC)C=C1O JFGFBYSYQKAFJF-UHFFFAOYSA-N 0.000 description 1
- NJEWTFJLELFYFK-UHFFFAOYSA-N (4-ethoxy-2-hydroxyphenyl)-(4-ethylphenyl)methanone Chemical compound OC1=CC(OCC)=CC=C1C(=O)C1=CC=C(CC)C=C1 NJEWTFJLELFYFK-UHFFFAOYSA-N 0.000 description 1
- IASKXZZHVHIYTR-UHFFFAOYSA-N (4-ethoxy-2-hydroxyphenyl)-(4-methoxyphenyl)methanone Chemical compound OC1=CC(OCC)=CC=C1C(=O)C1=CC=C(OC)C=C1 IASKXZZHVHIYTR-UHFFFAOYSA-N 0.000 description 1
- QHIOJMYBHOIVAV-UHFFFAOYSA-N (4-ethoxy-2-hydroxyphenyl)-(4-methylphenyl)methanone Chemical compound OC1=CC(OCC)=CC=C1C(=O)C1=CC=C(C)C=C1 QHIOJMYBHOIVAV-UHFFFAOYSA-N 0.000 description 1
- QIZJTIBDFGGTBF-UHFFFAOYSA-N (4-ethoxy-2-hydroxyphenyl)-(4-propoxyphenyl)methanone Chemical compound C1=CC(OCCC)=CC=C1C(=O)C1=CC=C(OCC)C=C1O QIZJTIBDFGGTBF-UHFFFAOYSA-N 0.000 description 1
- YUAPDZPOLLSUIM-UHFFFAOYSA-N (4-ethoxy-2-hydroxyphenyl)-(4-propylphenyl)methanone Chemical compound C1=CC(CCC)=CC=C1C(=O)C1=CC=C(OCC)C=C1O YUAPDZPOLLSUIM-UHFFFAOYSA-N 0.000 description 1
- JAFUHGPESJSRJX-UHFFFAOYSA-N (4-ethoxy-2-hydroxyphenyl)-phenylmethanone Chemical compound OC1=CC(OCC)=CC=C1C(=O)C1=CC=CC=C1 JAFUHGPESJSRJX-UHFFFAOYSA-N 0.000 description 1
- WDZDBUVSDXSDDC-UHFFFAOYSA-N (4-ethylphenyl)-(2-hydroxy-4-methoxyphenyl)methanone Chemical compound C1=CC(CC)=CC=C1C(=O)C1=CC=C(OC)C=C1O WDZDBUVSDXSDDC-UHFFFAOYSA-N 0.000 description 1
- BJEPYKJPYRNKOW-REOHCLBHSA-N (S)-malic acid Chemical compound OC(=O)[C@@H](O)CC(O)=O BJEPYKJPYRNKOW-REOHCLBHSA-N 0.000 description 1
- UTOVMEACOLCUCK-SNAWJCMRSA-N (e)-4-butoxy-4-oxobut-2-enoic acid Chemical compound CCCCOC(=O)\C=C\C(O)=O UTOVMEACOLCUCK-SNAWJCMRSA-N 0.000 description 1
- FIDRAVVQGKNYQK-UHFFFAOYSA-N 1,2,3,4-tetrahydrotriazine Chemical compound C1NNNC=C1 FIDRAVVQGKNYQK-UHFFFAOYSA-N 0.000 description 1
- YIYBRXKMQFDHSM-UHFFFAOYSA-N 2,2'-Dihydroxybenzophenone Chemical compound OC1=CC=CC=C1C(=O)C1=CC=CC=C1O YIYBRXKMQFDHSM-UHFFFAOYSA-N 0.000 description 1
- ZEOVXNVKXIPWMS-UHFFFAOYSA-N 2,2-dichloropropane Chemical compound CC(C)(Cl)Cl ZEOVXNVKXIPWMS-UHFFFAOYSA-N 0.000 description 1
- OWPUOLBODXJOKH-UHFFFAOYSA-N 2,3-dihydroxypropyl prop-2-enoate Chemical compound OCC(O)COC(=O)C=C OWPUOLBODXJOKH-UHFFFAOYSA-N 0.000 description 1
- AXCCTNWOXQEKQA-UHFFFAOYSA-N 2,4,6-triphenyl-2h-1,3,5-triazine-1,5,6-triamine Chemical compound NN1C(C=2C=CC=CC=2)N=C(C=2C=CC=CC=2)N(N)C1(N)C1=CC=CC=C1 AXCCTNWOXQEKQA-UHFFFAOYSA-N 0.000 description 1
- ZXDDPOHVAMWLBH-UHFFFAOYSA-N 2,4-Dihydroxybenzophenone Chemical compound OC1=CC(O)=CC=C1C(=O)C1=CC=CC=C1 ZXDDPOHVAMWLBH-UHFFFAOYSA-N 0.000 description 1
- MJFOVRMNLQNDDS-UHFFFAOYSA-N 2-(benzotriazol-2-yl)-4,6-dimethylphenol Chemical compound CC1=CC(C)=C(O)C(N2N=C3C=CC=CC3=N2)=C1 MJFOVRMNLQNDDS-UHFFFAOYSA-N 0.000 description 1
- CFZGXWYAUQYJEC-UHFFFAOYSA-N 2-(benzotriazol-2-yl)-4-cyclohexylphenol Chemical compound C1=C(N2N=C3C=CC=CC3=N2)C(O)=CC=C1C1CCCCC1 CFZGXWYAUQYJEC-UHFFFAOYSA-N 0.000 description 1
- NLWDAUDWBLSJGK-UHFFFAOYSA-N 2-(benzotriazol-2-yl)-4-tert-butyl-6-methylphenol Chemical compound CC1=CC(C(C)(C)C)=CC(N2N=C3C=CC=CC3=N2)=C1O NLWDAUDWBLSJGK-UHFFFAOYSA-N 0.000 description 1
- WXHVQMGINBSVAY-UHFFFAOYSA-N 2-(benzotriazol-2-yl)-4-tert-butylphenol Chemical compound CC(C)(C)C1=CC=C(O)C(N2N=C3C=CC=CC3=N2)=C1 WXHVQMGINBSVAY-UHFFFAOYSA-N 0.000 description 1
- RPQXCWCOHAKYBH-UHFFFAOYSA-N 2-(benzotriazol-2-yl)-6-methylphenol Chemical compound CC1=CC=CC(N2N=C3C=CC=CC3=N2)=C1O RPQXCWCOHAKYBH-UHFFFAOYSA-N 0.000 description 1
- ZBKCUYOBOGCDKC-UHFFFAOYSA-N 2-amino-6-phenyl-1h-1,3,5-triazin-4-one Chemical compound N1C(N)=NC(=O)N=C1C1=CC=CC=C1 ZBKCUYOBOGCDKC-UHFFFAOYSA-N 0.000 description 1
- POAOYUHQDCAZBD-UHFFFAOYSA-N 2-butoxyethanol Chemical compound CCCCOCCO POAOYUHQDCAZBD-UHFFFAOYSA-N 0.000 description 1
- AFXWHCJMTLWFKF-UHFFFAOYSA-N 2-chloropropanedioic acid Chemical compound OC(=O)C(Cl)C(O)=O AFXWHCJMTLWFKF-UHFFFAOYSA-N 0.000 description 1
- 229940093475 2-ethoxyethanol Drugs 0.000 description 1
- SVONRAPFKPVNKG-UHFFFAOYSA-N 2-ethoxyethyl acetate Chemical compound CCOCCOC(C)=O SVONRAPFKPVNKG-UHFFFAOYSA-N 0.000 description 1
- TZYRSLHNPKPEFV-UHFFFAOYSA-N 2-ethyl-1-butanol Chemical compound CCC(CC)CO TZYRSLHNPKPEFV-UHFFFAOYSA-N 0.000 description 1
- VHSHLMUCYSAUQU-UHFFFAOYSA-N 2-hydroxypropyl methacrylate Chemical compound CC(O)COC(=O)C(C)=C VHSHLMUCYSAUQU-UHFFFAOYSA-N 0.000 description 1
- LAMUXTNQCICZQX-UHFFFAOYSA-N 3-chloropropan-1-ol Chemical compound OCCCCl LAMUXTNQCICZQX-UHFFFAOYSA-N 0.000 description 1
- QOXOZONBQWIKDA-UHFFFAOYSA-N 3-hydroxypropyl Chemical group [CH2]CCO QOXOZONBQWIKDA-UHFFFAOYSA-N 0.000 description 1
- QCAWOHUJKPKOMD-UHFFFAOYSA-N 4,6-diamino-1h-pyrimidine-2-thione Chemical compound NC1=CC(N)=NC(S)=N1 QCAWOHUJKPKOMD-UHFFFAOYSA-N 0.000 description 1
- OGYSYXDNLPNNPW-UHFFFAOYSA-N 4-butoxy-4-oxobutanoic acid Chemical class CCCCOC(=O)CCC(O)=O OGYSYXDNLPNNPW-UHFFFAOYSA-N 0.000 description 1
- 125000004172 4-methoxyphenyl group Chemical group [H]C1=C([H])C(OC([H])([H])[H])=C([H])C([H])=C1* 0.000 description 1
- VGVHNLRUAMRIEW-UHFFFAOYSA-N 4-methylcyclohexan-1-one Chemical compound CC1CCC(=O)CC1 VGVHNLRUAMRIEW-UHFFFAOYSA-N 0.000 description 1
- IEMHIOUNBGZEAG-UHFFFAOYSA-N 4-tert-butyl-2-(5-chlorobenzotriazol-2-yl)phenol Chemical compound CC(C)(C)C1=CC=C(O)C(N2N=C3C=C(Cl)C=CC3=N2)=C1 IEMHIOUNBGZEAG-UHFFFAOYSA-N 0.000 description 1
- GAUKJEIXDYZROX-UHFFFAOYSA-N 6,10-dihydroxydecyl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OCCCCCC(O)CCCCO GAUKJEIXDYZROX-UHFFFAOYSA-N 0.000 description 1
- FVFVNNKYKYZTJU-UHFFFAOYSA-N 6-chloro-1,3,5-triazine-2,4-diamine Chemical compound NC1=NC(N)=NC(Cl)=N1 FVFVNNKYKYZTJU-UHFFFAOYSA-N 0.000 description 1
- GZVHEAJQGPRDLQ-UHFFFAOYSA-N 6-phenyl-1,3,5-triazine-2,4-diamine Chemical compound NC1=NC(N)=NC(C=2C=CC=CC=2)=N1 GZVHEAJQGPRDLQ-UHFFFAOYSA-N 0.000 description 1
- 229930003347 Atropine Natural products 0.000 description 1
- ZNSMNVMLTJELDZ-UHFFFAOYSA-N Bis(2-chloroethyl)ether Chemical compound ClCCOCCCl ZNSMNVMLTJELDZ-UHFFFAOYSA-N 0.000 description 1
- FERIUCNNQQJTOY-UHFFFAOYSA-M Butyrate Chemical compound CCCC([O-])=O FERIUCNNQQJTOY-UHFFFAOYSA-M 0.000 description 1
- QGDSPAPQURDOCF-UHFFFAOYSA-N C1=CC(O)(O)CC(O)=C1C(=O)C1=CC=CC=C1O Chemical compound C1=CC(O)(O)CC(O)=C1C(=O)C1=CC=CC=C1O QGDSPAPQURDOCF-UHFFFAOYSA-N 0.000 description 1
- OFOKEYMAWJYJPM-UHFFFAOYSA-N CCCCOC1=CC(CC=C1C(=O)C2=CC=CC=C2O)(OCCCC)OCCCC Chemical compound CCCCOC1=CC(CC=C1C(=O)C2=CC=CC=C2O)(OCCCC)OCCCC OFOKEYMAWJYJPM-UHFFFAOYSA-N 0.000 description 1
- WNIDKRXWYMVHBH-UHFFFAOYSA-N CCOC1(CC=C(C=C1)C(=O)C2=CC=CC=C2O)OCC Chemical compound CCOC1(CC=C(C=C1)C(=O)C2=CC=CC=C2O)OCC WNIDKRXWYMVHBH-UHFFFAOYSA-N 0.000 description 1
- OXKAVCLNLCUDCY-UHFFFAOYSA-N CCOC1=CC(=C(C=C1)C(=O)C2=CC=C(C=C2)C(C)(C)C)O Chemical compound CCOC1=CC(=C(C=C1)C(=O)C2=CC=C(C=C2)C(C)(C)C)O OXKAVCLNLCUDCY-UHFFFAOYSA-N 0.000 description 1
- IWWLEZKPTIXZCC-UHFFFAOYSA-N COC1(C=CC(=CC1O)C(=O)C2=CC=CC=C2O)OC Chemical compound COC1(C=CC(=CC1O)C(=O)C2=CC=CC=C2O)OC IWWLEZKPTIXZCC-UHFFFAOYSA-N 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- XDTMQSROBMDMFD-UHFFFAOYSA-N Cyclohexane Chemical compound C1CCCCC1 XDTMQSROBMDMFD-UHFFFAOYSA-N 0.000 description 1
- JYFHYPJRHGVZDY-UHFFFAOYSA-N Dibutyl phosphate Chemical compound CCCCOP(O)(=O)OCCCC JYFHYPJRHGVZDY-UHFFFAOYSA-N 0.000 description 1
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 1
- 239000005977 Ethylene Substances 0.000 description 1
- KMTRUDSVKNLOMY-UHFFFAOYSA-N Ethylene carbonate Chemical compound O=C1OCCO1 KMTRUDSVKNLOMY-UHFFFAOYSA-N 0.000 description 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
- RKUNBYITZUJHSG-UHFFFAOYSA-N Hyosciamin-hydrochlorid Natural products CN1C(C2)CCC1CC2OC(=O)C(CO)C1=CC=CC=C1 RKUNBYITZUJHSG-UHFFFAOYSA-N 0.000 description 1
- VQTUBCCKSQIDNK-UHFFFAOYSA-N Isobutene Chemical group CC(C)=C VQTUBCCKSQIDNK-UHFFFAOYSA-N 0.000 description 1
- YZBOVSFWWNVKRJ-UHFFFAOYSA-N Monobutylphthalate Chemical class CCCCOC(=O)C1=CC=CC=C1C(O)=O YZBOVSFWWNVKRJ-UHFFFAOYSA-N 0.000 description 1
- MGJKQDOBUOMPEZ-UHFFFAOYSA-N N,N'-dimethylurea Chemical compound CNC(=O)NC MGJKQDOBUOMPEZ-UHFFFAOYSA-N 0.000 description 1
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 1
- NPAJRRQMUWPIRR-UHFFFAOYSA-N OC1=C(C(=O)C2=C(C=CC=C2)O)C=CC(C1)(OCCC)OCCC Chemical compound OC1=C(C(=O)C2=C(C=CC=C2)O)C=CC(C1)(OCCC)OCCC NPAJRRQMUWPIRR-UHFFFAOYSA-N 0.000 description 1
- XIJYYKHPBOMMNZ-UHFFFAOYSA-N OC1=C(C(=O)C2=C(C=CC=C2)O)C=CC(C1)(OCCCC)OCCCC Chemical compound OC1=C(C(=O)C2=C(C=CC=C2)O)C=CC(C1)(OCCCC)OCCCC XIJYYKHPBOMMNZ-UHFFFAOYSA-N 0.000 description 1
- 239000004793 Polystyrene Substances 0.000 description 1
- XBDQKXXYIPTUBI-UHFFFAOYSA-M Propionate Chemical compound CCC([O-])=O XBDQKXXYIPTUBI-UHFFFAOYSA-M 0.000 description 1
- 240000004808 Saccharomyces cerevisiae Species 0.000 description 1
- 241000779819 Syncarpia glomulifera Species 0.000 description 1
- 241001336778 Thapsia Species 0.000 description 1
- 229920001807 Urea-formaldehyde Polymers 0.000 description 1
- IKHGUXGNUITLKF-XPULMUKRSA-N acetaldehyde Chemical compound [14CH]([14CH3])=O IKHGUXGNUITLKF-XPULMUKRSA-N 0.000 description 1
- 150000001242 acetic acid derivatives Chemical class 0.000 description 1
- KXKVLQRXCPHEJC-UHFFFAOYSA-N acetic acid trimethyl ester Natural products COC(C)=O KXKVLQRXCPHEJC-UHFFFAOYSA-N 0.000 description 1
- NJYZCEFQAIUHSD-UHFFFAOYSA-N acetoguanamine Chemical compound CC1=NC(N)=NC(N)=N1 NJYZCEFQAIUHSD-UHFFFAOYSA-N 0.000 description 1
- 150000001252 acrylic acid derivatives Chemical class 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 239000002390 adhesive tape Substances 0.000 description 1
- 230000001476 alcoholic effect Effects 0.000 description 1
- 125000001931 aliphatic group Chemical group 0.000 description 1
- 125000002947 alkylene group Chemical group 0.000 description 1
- 229910000147 aluminium phosphate Inorganic materials 0.000 description 1
- 150000001408 amides Chemical class 0.000 description 1
- 150000001414 amino alcohols Chemical class 0.000 description 1
- 125000003277 amino group Chemical group 0.000 description 1
- 229920003180 amino resin Polymers 0.000 description 1
- MASBWURJQFFLOO-UHFFFAOYSA-N ammeline Chemical compound NC1=NC(N)=NC(O)=N1 MASBWURJQFFLOO-UHFFFAOYSA-N 0.000 description 1
- 229940072049 amyl acetate Drugs 0.000 description 1
- PGMYKACGEOXYJE-UHFFFAOYSA-N anhydrous amyl acetate Natural products CCCCCOC(C)=O PGMYKACGEOXYJE-UHFFFAOYSA-N 0.000 description 1
- 239000003963 antioxidant agent Substances 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- RKUNBYITZUJHSG-SPUOUPEWSA-N atropine Chemical compound O([C@H]1C[C@H]2CC[C@@H](C1)N2C)C(=O)C(CO)C1=CC=CC=C1 RKUNBYITZUJHSG-SPUOUPEWSA-N 0.000 description 1
- 229960000396 atropine Drugs 0.000 description 1
- NHDLVKOYPQPGNT-UHFFFAOYSA-N benzene-1,2,3,5-tetracarboxylic acid Chemical compound OC(=O)C1=CC(C(O)=O)=C(C(O)=O)C(C(O)=O)=C1 NHDLVKOYPQPGNT-UHFFFAOYSA-N 0.000 description 1
- 150000008366 benzophenones Chemical class 0.000 description 1
- QRUDEWIWKLJBPS-UHFFFAOYSA-N benzotriazole Chemical compound C1=CC=C2N[N][N]C2=C1 QRUDEWIWKLJBPS-UHFFFAOYSA-N 0.000 description 1
- 235000019445 benzyl alcohol Nutrition 0.000 description 1
- RJNJWHFSKNJCTB-UHFFFAOYSA-N benzylurea Chemical compound NC(=O)NCC1=CC=CC=C1 RJNJWHFSKNJCTB-UHFFFAOYSA-N 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 239000004305 biphenyl Substances 0.000 description 1
- SODJJEXAWOSSON-UHFFFAOYSA-N bis(2-hydroxy-4-methoxyphenyl)methanone Chemical compound OC1=CC(OC)=CC=C1C(=O)C1=CC=C(OC)C=C1O SODJJEXAWOSSON-UHFFFAOYSA-N 0.000 description 1
- PQTPKDRDZXZVND-UHFFFAOYSA-N bis(4-ethoxy-2-hydroxyphenyl)methanone Chemical compound OC1=CC(OCC)=CC=C1C(=O)C1=CC=C(OCC)C=C1O PQTPKDRDZXZVND-UHFFFAOYSA-N 0.000 description 1
- 229940043232 butyl acetate Drugs 0.000 description 1
- BNMJSBUIDQYHIN-UHFFFAOYSA-N butyl dihydrogen phosphate Chemical class CCCCOP(O)(O)=O BNMJSBUIDQYHIN-UHFFFAOYSA-N 0.000 description 1
- 239000004202 carbamide Substances 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- BVKZGUZCCUSVTD-UHFFFAOYSA-N carbonic acid Chemical class OC(O)=O BVKZGUZCCUSVTD-UHFFFAOYSA-N 0.000 description 1
- 238000005266 casting Methods 0.000 description 1
- 239000004359 castor oil Substances 0.000 description 1
- 235000019438 castor oil Nutrition 0.000 description 1
- 229920006217 cellulose acetate butyrate Polymers 0.000 description 1
- 150000008280 chlorinated hydrocarbons Chemical class 0.000 description 1
- 238000004140 cleaning Methods 0.000 description 1
- 229920001688 coating polymer Polymers 0.000 description 1
- 239000004020 conductor Substances 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 239000007799 cork Substances 0.000 description 1
- MLUCVPSAIODCQM-NSCUHMNNSA-N crotonaldehyde Chemical compound C\C=C\C=O MLUCVPSAIODCQM-NSCUHMNNSA-N 0.000 description 1
- MLUCVPSAIODCQM-UHFFFAOYSA-N crotonaldehyde Natural products CC=CC=O MLUCVPSAIODCQM-UHFFFAOYSA-N 0.000 description 1
- LDHQCZJRKDOVOX-NSCUHMNNSA-N crotonic acid Chemical class C\C=C\C(O)=O LDHQCZJRKDOVOX-NSCUHMNNSA-N 0.000 description 1
- NBBUYPNTAABDEY-UHFFFAOYSA-N cyclobutane-1,1-diol Chemical compound OC1(O)CCC1 NBBUYPNTAABDEY-UHFFFAOYSA-N 0.000 description 1
- 230000000593 degrading effect Effects 0.000 description 1
- 150000004891 diazines Chemical class 0.000 description 1
- 150000001991 dicarboxylic acids Chemical class 0.000 description 1
- QGBSISYHAICWAH-UHFFFAOYSA-N dicyandiamide Chemical compound NC(N)=NC#N QGBSISYHAICWAH-UHFFFAOYSA-N 0.000 description 1
- VOUQVWQRJJVRFU-UHFFFAOYSA-N diethyl 2-[(4-methoxyphenyl)methyl]propanedioate Chemical compound CCOC(=O)C(C(=O)OCC)CC1=CC=C(OC)C=C1 VOUQVWQRJJVRFU-UHFFFAOYSA-N 0.000 description 1
- KUBLMWHFTKNBHL-UHFFFAOYSA-N diethyl 2-[(4-methoxyphenyl)methylidene]propanedioate Chemical compound CCOC(=O)C(C(=O)OCC)=CC1=CC=C(OC)C=C1 KUBLMWHFTKNBHL-UHFFFAOYSA-N 0.000 description 1
- 125000004177 diethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- XXJWXESWEXIICW-UHFFFAOYSA-N diethylene glycol monoethyl ether Chemical class CCOCCOCCO XXJWXESWEXIICW-UHFFFAOYSA-N 0.000 description 1
- 125000000118 dimethyl group Chemical group [H]C([H])([H])* 0.000 description 1
- 238000007598 dipping method Methods 0.000 description 1
- WNAHIZMDSQCWRP-UHFFFAOYSA-N dodecane-1-thiol Chemical compound CCCCCCCCCCCCS WNAHIZMDSQCWRP-UHFFFAOYSA-N 0.000 description 1
- 229920001971 elastomer Polymers 0.000 description 1
- 238000006266 etherification reaction Methods 0.000 description 1
- 150000002170 ethers Chemical class 0.000 description 1
- 238000011156 evaluation Methods 0.000 description 1
- 239000000945 filler Substances 0.000 description 1
- 239000001530 fumaric acid Substances 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 235000011187 glycerol Nutrition 0.000 description 1
- ZEMPKEQAKRGZGQ-XOQCFJPHSA-N glycerol triricinoleate Natural products CCCCCC[C@@H](O)CC=CCCCCCCCC(=O)OC[C@@H](COC(=O)CCCCCCCC=CC[C@@H](O)CCCCCC)OC(=O)CCCCCCCC=CC[C@H](O)CCCCCC ZEMPKEQAKRGZGQ-XOQCFJPHSA-N 0.000 description 1
- 150000002334 glycols Chemical class 0.000 description 1
- 239000008187 granular material Substances 0.000 description 1
- 150000002357 guanidines Chemical class 0.000 description 1
- 125000005843 halogen group Chemical group 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- MNWFXJYAOYHMED-UHFFFAOYSA-M heptanoate Chemical compound CCCCCCC([O-])=O MNWFXJYAOYHMED-UHFFFAOYSA-M 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 125000002768 hydroxyalkyl group Chemical group 0.000 description 1
- 238000009863 impact test Methods 0.000 description 1
- 208000015181 infectious disease Diseases 0.000 description 1
- 125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 description 1
- JMMWKPVZQRWMSS-UHFFFAOYSA-N isopropanol acetate Natural products CC(C)OC(C)=O JMMWKPVZQRWMSS-UHFFFAOYSA-N 0.000 description 1
- 229940011051 isopropyl acetate Drugs 0.000 description 1
- GWYFCOCPABKNJV-UHFFFAOYSA-M isovalerate Chemical compound CC(C)CC([O-])=O GWYFCOCPABKNJV-UHFFFAOYSA-M 0.000 description 1
- LVHBHZANLOWSRM-UHFFFAOYSA-N itaconic acid Chemical class OC(=O)CC(=C)C(O)=O LVHBHZANLOWSRM-UHFFFAOYSA-N 0.000 description 1
- 238000003475 lamination Methods 0.000 description 1
- PBOSTUDLECTMNL-UHFFFAOYSA-N lauryl acrylate Chemical class CCCCCCCCCCCCOC(=O)C=C PBOSTUDLECTMNL-UHFFFAOYSA-N 0.000 description 1
- 230000014759 maintenance of location Effects 0.000 description 1
- 229940049920 malate Drugs 0.000 description 1
- 150000002688 maleic acid derivatives Chemical class 0.000 description 1
- 239000001630 malic acid Substances 0.000 description 1
- 235000011090 malic acid Nutrition 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- GYNNXHKOJHMOHS-UHFFFAOYSA-N methyl-cycloheptane Natural products CC1CCCCCC1 GYNNXHKOJHMOHS-UHFFFAOYSA-N 0.000 description 1
- MJVGBKJNTFCUJM-UHFFFAOYSA-N mexenone Chemical compound OC1=CC(OC)=CC=C1C(=O)C1=CC=C(C)C=C1 MJVGBKJNTFCUJM-UHFFFAOYSA-N 0.000 description 1
- 239000002480 mineral oil Substances 0.000 description 1
- 238000000465 moulding Methods 0.000 description 1
- YKYONYBAUNKHLG-UHFFFAOYSA-N n-Propyl acetate Natural products CCCOC(C)=O YKYONYBAUNKHLG-UHFFFAOYSA-N 0.000 description 1
- 150000002825 nitriles Chemical class 0.000 description 1
- BDJRBEYXGGNYIS-UHFFFAOYSA-N nonanedioic acid Chemical compound OC(=O)CCCCCCCC(O)=O BDJRBEYXGGNYIS-UHFFFAOYSA-N 0.000 description 1
- TVMXDCGIABBOFY-UHFFFAOYSA-N octane Chemical compound CCCCCCCC TVMXDCGIABBOFY-UHFFFAOYSA-N 0.000 description 1
- 125000001820 oxy group Chemical group [*:1]O[*:2] 0.000 description 1
- DXGLGDHPHMLXJC-UHFFFAOYSA-N oxybenzone Chemical compound OC1=CC(OC)=CC=C1C(=O)C1=CC=CC=C1 DXGLGDHPHMLXJC-UHFFFAOYSA-N 0.000 description 1
- 239000003973 paint Substances 0.000 description 1
- QNGNSVIICDLXHT-UHFFFAOYSA-N para-ethylbenzaldehyde Natural products CCC1=CC=C(C=O)C=C1 QNGNSVIICDLXHT-UHFFFAOYSA-N 0.000 description 1
- 230000035515 penetration Effects 0.000 description 1
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 description 1
- 239000010452 phosphate Substances 0.000 description 1
- 150000003013 phosphoric acid derivatives Chemical class 0.000 description 1
- 239000001739 pinus spp. Substances 0.000 description 1
- 229920001225 polyester resin Polymers 0.000 description 1
- 239000004645 polyester resin Substances 0.000 description 1
- 238000006116 polymerization reaction Methods 0.000 description 1
- 229920002223 polystyrene Polymers 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- 229940090181 propyl acetate Drugs 0.000 description 1
- RUOJZAUFBMNUDX-UHFFFAOYSA-N propylene carbonate Chemical compound CC1COC(=O)O1 RUOJZAUFBMNUDX-UHFFFAOYSA-N 0.000 description 1
- CSNFMBGHUOSBFU-UHFFFAOYSA-N pyrimidine-2,4,5-triamine Chemical compound NC1=NC=C(N)C(N)=N1 CSNFMBGHUOSBFU-UHFFFAOYSA-N 0.000 description 1
- 230000005855 radiation Effects 0.000 description 1
- 230000035484 reaction time Effects 0.000 description 1
- 238000011084 recovery Methods 0.000 description 1
- 238000010992 reflux Methods 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 238000007127 saponification reaction Methods 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 238000009991 scouring Methods 0.000 description 1
- 229920002545 silicone oil Polymers 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- 125000001424 substituent group Chemical group 0.000 description 1
- 150000003900 succinic acid esters Chemical class 0.000 description 1
- 150000005846 sugar alcohols Polymers 0.000 description 1
- 239000002344 surface layer Substances 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
- 238000011282 treatment Methods 0.000 description 1
- 150000003918 triazines Chemical class 0.000 description 1
- HUUBMTMJIQHAEN-UHFFFAOYSA-N triazole-1,4-diamine Chemical compound NC1=CN(N)N=N1 HUUBMTMJIQHAEN-UHFFFAOYSA-N 0.000 description 1
- 150000003852 triazoles Chemical class 0.000 description 1
- 229940036248 turpentine Drugs 0.000 description 1
- NQPDZGIKBAWPEJ-UHFFFAOYSA-N valeric acid Chemical compound CCCCC(O)=O NQPDZGIKBAWPEJ-UHFFFAOYSA-N 0.000 description 1
- 239000002966 varnish Substances 0.000 description 1
- 239000008096 xylene Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
- C09D167/00—Coating compositions based on polyesters obtained by reactions forming a carboxylic ester link in the main chain; Coating compositions based on derivatives of such polymers
- C09D167/04—Polyesters derived from hydroxycarboxylic acids, e.g. lactones
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J7/00—Chemical treatment or coating of shaped articles made of macromolecular substances
- C08J7/04—Coating
- C08J7/0427—Coating with only one layer of a composition containing a polymer binder
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J7/00—Chemical treatment or coating of shaped articles made of macromolecular substances
- C08J7/04—Coating
- C08J7/043—Improving the adhesiveness of the coatings per se, e.g. forming primers
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J7/00—Chemical treatment or coating of shaped articles made of macromolecular substances
- C08J7/04—Coating
- C08J7/046—Forming abrasion-resistant coatings; Forming surface-hardening coatings
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J2369/00—Characterised by the use of polycarbonates; Derivatives of polycarbonates
-
- 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]
- Y10T428/31507—Of polycarbonate
-
- 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]
- Y10T428/31786—Of polyester [e.g., alkyd, etc.]
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Polymers & Plastics (AREA)
- Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Materials Engineering (AREA)
- Wood Science & Technology (AREA)
- Engineering & Computer Science (AREA)
- Life Sciences & Earth Sciences (AREA)
- Paints Or Removers (AREA)
- Laminated Bodies (AREA)
- Polyesters Or Polycarbonates (AREA)
- Coating Of Shaped Articles Made Of Macromolecular Substances (AREA)
- Compositions Of Macromolecular Compounds (AREA)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US24560572 | 1972-04-19 | ||
US00245605A US3843390A (en) | 1972-04-19 | 1972-04-19 | Coated polycarbonates |
Publications (2)
Publication Number | Publication Date |
---|---|
FI57436B FI57436B (fi) | 1980-04-30 |
FI57436C true FI57436C (fi) | 1980-08-11 |
Family
ID=22927367
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
FI1221/73A FI57436C (fi) | 1972-04-19 | 1973-04-17 | Anvaendning av en pao akrylharts baserad belaeggning foer utbelaeggning av ett polykarbonatsubstrat |
Country Status (21)
Country | Link |
---|---|
US (1) | US3843390A (en:Method) |
JP (1) | JPS5411833B2 (en:Method) |
AR (1) | AR197501A1 (en:Method) |
AT (1) | AT333912B (en:Method) |
AU (1) | AU469171B2 (en:Method) |
BE (1) | BE798402A (en:Method) |
BR (1) | BR7302779D0 (en:Method) |
CA (1) | CA1011032A (en:Method) |
CH (1) | CH591536A5 (en:Method) |
DE (1) | DE2317874C3 (en:Method) |
ES (1) | ES413810A1 (en:Method) |
FI (1) | FI57436C (en:Method) |
FR (1) | FR2181028B1 (en:Method) |
GB (1) | GB1417502A (en:Method) |
IE (1) | IE37537B1 (en:Method) |
IN (1) | IN139781B (en:Method) |
IT (1) | IT980267B (en:Method) |
NL (1) | NL174062B (en:Method) |
NO (1) | NO137756C (en:Method) |
SE (1) | SE396086B (en:Method) |
ZA (1) | ZA732669B (en:Method) |
Families Citing this family (35)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
FR2306243A1 (fr) * | 1975-04-03 | 1976-10-29 | Asahi Dow Ltd | Composition de revetement hydrophyle |
US3979540A (en) * | 1975-12-22 | 1976-09-07 | E. I. Du Pont De Nemours And Company | Ionomer resin substrates coated with an epoxy primer and finished with an acrylic coating |
CA1091106A (en) * | 1976-03-22 | 1980-12-09 | Joseph M. Rich | Coated polycarbonates |
US4103065A (en) * | 1976-08-12 | 1978-07-25 | Owens-Illinois, Inc. | Coated polycarbonates and acrylics |
DE2717164C2 (de) * | 1977-04-19 | 1986-05-07 | Bayer Ag, 5090 Leverkusen | Überzugsmittel für Polycarbonate |
DE2725317A1 (de) * | 1977-06-04 | 1978-12-14 | Bayer Ag | Kratz- und wetterfeste verbundsysteme auf basis polycarbonat |
US4146658A (en) * | 1978-04-12 | 1979-03-27 | General Electric Company | Process for producing an ultraviolet light stabilized polycarbonate article |
US4148842A (en) * | 1978-06-15 | 1979-04-10 | Stauffer Chemical Company | Blends of a polycarbonate resin and interpolymer modifier |
US4201832A (en) * | 1978-06-23 | 1980-05-06 | General Electric Company | Non melt-drip flame retardant polycarbonate composition |
US4384026A (en) * | 1978-11-01 | 1983-05-17 | General Electric Company | Photocurable acrylic coated polycarbonate articles |
US4242383A (en) * | 1979-04-18 | 1980-12-30 | General Electric Company | Method of providing a polycarbonate article with a uniform and durable organopolysiloxane coating |
US4242381A (en) * | 1979-04-18 | 1980-12-30 | General Electric Company | Method of providing a polycarbonate article with a uniform and durable silica filled organopolysiloxane coating |
FR2483448B1 (fr) * | 1980-05-29 | 1985-12-20 | Nippon Sheet Glass Co Ltd | Composition de revetement antibuee, article faconne revetu de cette composition et procede de preparation de cet article |
US4366207A (en) * | 1981-03-09 | 1982-12-28 | General Electric Company | Polycarbonate resins stabilized with nitriles containing a 2-OH benzophenone group |
DE3151350A1 (de) * | 1981-12-24 | 1983-07-07 | Bayer Ag, 5090 Leverkusen | Mit einem 3-schichtueberzug ausgeruestete kunststofformkoerper und ein verfahren zur herstellung der ausruestung |
CA1239492A (en) * | 1982-10-18 | 1988-07-19 | Donald F. Smith, Jr. | High solids coating compositions containing polycaprolactone polyol reactive diluents |
US4751112A (en) * | 1982-10-18 | 1988-06-14 | Union Carbide Corporation | High solids coating compositions containing polycaprolactone polyol reactive diluents |
DE3439482A1 (de) * | 1984-10-27 | 1986-05-07 | Röhm GmbH, 6100 Darmstadt | Verfahren zur beschichtung von substraten mit kratzfesten, nichtreflektierenden ueberzuegen |
US4714657A (en) * | 1985-04-18 | 1987-12-22 | General Electric Company | Melamine based protective coatings for thermoplastic substrates |
CA1293436C (en) * | 1985-11-01 | 1991-12-24 | Jack Henry Witman | Stain and scratch resistant resilient surface coverings |
US4795783A (en) * | 1987-06-19 | 1989-01-03 | Ppg Industries, Inc. | Organopolysiloxane containing coating compositions |
US5380076A (en) * | 1990-02-14 | 1995-01-10 | Kabushiki Kaisha Komatsu Seisakusho | Rubber crawler belt of a tracked vehicle |
DE4124806A1 (de) * | 1991-07-26 | 1993-01-28 | Bayer Ag | Verfahren zum beschichten von polycarbonatformkoerpern |
US5412038A (en) * | 1993-06-28 | 1995-05-02 | Union Carbide Chemicals & Plastics Technology Corporation | Process utilizing alkenylcarboxylate crosslinkers |
US5443877A (en) * | 1994-03-01 | 1995-08-22 | General Electric Company | Glazing laminate having a replaceable sacrificial layer |
EP0714764A3 (en) | 1994-12-02 | 1997-03-05 | Gen Electric | Improved impact resistant composite |
US6824849B2 (en) | 2000-08-07 | 2004-11-30 | 3M Innovative Properties Company | Laser-cuttable multi-layer sheet material |
US7370903B2 (en) | 2002-05-10 | 2008-05-13 | United Protective Technologies, Llc | Transparent laminated structure having peel-away film layers for use on aircraft windscreens |
US8322775B1 (en) | 2002-05-10 | 2012-12-04 | Vtol, Llc | Transparent laminated structure having peel-away film layers for use on aircraft windscreens |
US7960031B2 (en) * | 2004-06-30 | 2011-06-14 | Sabic Innovative Plastics Ip B.V. | Coated sheet, method of formation thereof, and articles derived therefrom |
US9078956B2 (en) * | 2010-06-10 | 2015-07-14 | Econous Systems Inc. | Modification of biomedical polymers for prevention of fouling and clotting |
JP5855107B2 (ja) | 2010-09-17 | 2016-02-09 | エボニック レーム ゲゼルシャフト ミット ベシュレンクテル ハフツングEvonik Roehm GmbH | 改善された光沢及び耐擦性を有する、耐候性の染色された成形体 |
GB2515811B (en) * | 2013-07-05 | 2015-11-11 | Dyson Technology Ltd | A handheld appliance |
FR3021158B1 (fr) * | 2014-05-19 | 2017-12-15 | Nexans | Utilisation d’un solvant polaire aprotique en tant que fluide d’interface entre un cable electrique et un accessoire |
EP3772527A1 (de) | 2019-08-08 | 2021-02-10 | Evonik Operations GmbH | Durchsichtige zusammensetzung |
-
1972
- 1972-04-19 US US00245605A patent/US3843390A/en not_active Expired - Lifetime
-
1973
- 1973-03-08 CA CA165,632A patent/CA1011032A/en not_active Expired
- 1973-04-09 IN IN828/CAL/73A patent/IN139781B/en unknown
- 1973-04-10 DE DE2317874A patent/DE2317874C3/de not_active Expired
- 1973-04-13 AU AU54490/73A patent/AU469171B2/en not_active Expired
- 1973-04-16 NL NLAANVRAGE7305310,A patent/NL174062B/xx not_active IP Right Cessation
- 1973-04-17 BR BR732779A patent/BR7302779D0/pt unknown
- 1973-04-17 SE SE7305464A patent/SE396086B/xx unknown
- 1973-04-17 IE IE603/73A patent/IE37537B1/xx unknown
- 1973-04-17 JP JP4275073A patent/JPS5411833B2/ja not_active Expired
- 1973-04-17 ES ES413810A patent/ES413810A1/es not_active Expired
- 1973-04-17 NO NO1643/73A patent/NO137756C/no unknown
- 1973-04-17 AT AT340773A patent/AT333912B/de not_active IP Right Cessation
- 1973-04-17 FI FI1221/73A patent/FI57436C/fi active
- 1973-04-18 AR AR247619A patent/AR197501A1/es active
- 1973-04-18 BE BE130165A patent/BE798402A/xx not_active IP Right Cessation
- 1973-04-18 IT IT49522/73A patent/IT980267B/it active
- 1973-04-18 ZA ZA732669A patent/ZA732669B/xx unknown
- 1973-04-18 CH CH562373A patent/CH591536A5/xx not_active IP Right Cessation
- 1973-04-19 GB GB1899173A patent/GB1417502A/en not_active Expired
- 1973-04-19 FR FR7314435A patent/FR2181028B1/fr not_active Expired
Also Published As
Publication number | Publication date |
---|---|
JPS5411833B2 (en:Method) | 1979-05-17 |
ATA340773A (de) | 1976-04-15 |
IN139781B (en:Method) | 1976-07-31 |
IE37537L (en) | 1973-10-19 |
NL7305310A (en:Method) | 1973-10-23 |
IT980267B (it) | 1974-09-30 |
DE2317874A1 (de) | 1973-10-25 |
DE2317874B2 (de) | 1980-10-16 |
AT333912B (de) | 1976-12-27 |
JPS4920229A (en:Method) | 1974-02-22 |
NO137756B (no) | 1978-01-09 |
FR2181028B1 (en:Method) | 1976-11-12 |
ES413810A1 (es) | 1976-01-16 |
SE396086B (sv) | 1977-09-05 |
FI57436B (fi) | 1980-04-30 |
CH591536A5 (en:Method) | 1977-09-30 |
CA1011032A (en) | 1977-05-24 |
BE798402A (fr) | 1973-10-18 |
AU5449073A (en) | 1974-10-17 |
BR7302779D0 (pt) | 1974-08-15 |
FR2181028A1 (en:Method) | 1973-11-30 |
NO137756C (no) | 1978-04-19 |
DE2317874C3 (de) | 1981-07-30 |
AU469171B2 (en) | 1976-02-05 |
IE37537B1 (en) | 1977-08-17 |
NL174062B (nl) | 1983-11-16 |
US3843390A (en) | 1974-10-22 |
ZA732669B (en) | 1974-03-27 |
GB1417502A (en) | 1975-12-10 |
AR197501A1 (es) | 1974-04-15 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
FI57436C (fi) | Anvaendning av en pao akrylharts baserad belaeggning foer utbelaeggning av ett polykarbonatsubstrat | |
US4076766A (en) | Flexible thermosetting acrylic enamels | |
US4546046A (en) | Substrates with flexible coatings from epsilon-caprolactone modified acrylics | |
CA2186871C (en) | Resin composition for hard coating, coated product and surface-coated vessel and process for producing same | |
US4714657A (en) | Melamine based protective coatings for thermoplastic substrates | |
US5136000A (en) | Methods for preparing and using a water dilutable copolymer and aqueous coating composition prepared therewith | |
CA1227298A (en) | High solids polymer resin coating composition containing amino resin cross-linking agent | |
JPH06506718A (ja) | Uv硬化性ハードコート組成物と製造方法 | |
EP0100688A2 (en) | Curable coating composition | |
CN112831242B (zh) | 一种氨基树脂醇酸消光漆 | |
US4319016A (en) | Ultraviolet-absorbing amino compound and method of making | |
CA2103813A1 (en) | Coating weatherability by uv radiation exposure | |
US4552936A (en) | Weatherable abrasion resistant etherified aminoplast derived coating for plastic substrates | |
US4681815A (en) | Coating composition of polyester oligomer and acrylic binder | |
US4720528A (en) | Substrates with flexible coatings from epsilon-caprolactone modified acrylics | |
EP1263900B1 (en) | Melamine coating compositions | |
JPH0557309B2 (en:Method) | ||
JP5283305B2 (ja) | 金属化処理用アンダーコート層形成用被覆組成物 | |
CA1091106A (en) | Coated polycarbonates | |
US4598021A (en) | Weatherable abrasion resistant etherified aminoplast derived coating for plastic substrates | |
EP0274466A1 (en) | Melamine based protective coatings for thermoplastic substrates | |
JPH0414149B2 (en:Method) | ||
JPH0324506B2 (en:Method) | ||
JPH0413391B2 (en:Method) | ||
JPH0553837B2 (en:Method) |