NO762703L - - Google Patents
Info
- Publication number
- NO762703L NO762703L NO762703A NO762703A NO762703L NO 762703 L NO762703 L NO 762703L NO 762703 A NO762703 A NO 762703A NO 762703 A NO762703 A NO 762703A NO 762703 L NO762703 L NO 762703L
- Authority
- NO
- Norway
- Prior art keywords
- acids
- resins
- printing
- printing inks
- binder
- Prior art date
Links
- 238000007639 printing Methods 0.000 claims description 63
- 239000000976 ink Substances 0.000 claims description 38
- 239000011230 binding agent Substances 0.000 claims description 29
- 238000000034 method Methods 0.000 claims description 29
- -1 cyclic anhydrides Chemical class 0.000 claims description 23
- 239000011347 resin Substances 0.000 claims description 23
- 229920005989 resin Polymers 0.000 claims description 23
- 229920006122 polyamide resin Polymers 0.000 claims description 22
- 150000004985 diamines Chemical class 0.000 claims description 21
- 235000014113 dietary fatty acids Nutrition 0.000 claims description 18
- 239000000194 fatty acid Substances 0.000 claims description 18
- 229930195729 fatty acid Natural products 0.000 claims description 18
- 150000004665 fatty acids Chemical class 0.000 claims description 17
- 239000000203 mixture Substances 0.000 claims description 17
- 125000004432 carbon atom Chemical group C* 0.000 claims description 14
- 150000002763 monocarboxylic acids Chemical class 0.000 claims description 14
- 239000000049 pigment Substances 0.000 claims description 14
- 229920006149 polyester-amide block copolymer Polymers 0.000 claims description 12
- 150000002009 diols Chemical class 0.000 claims description 8
- KKEYFWRCBNTPAC-UHFFFAOYSA-N Terephthalic acid Chemical compound OC(=O)C1=CC=C(C(O)=O)C=C1 KKEYFWRCBNTPAC-UHFFFAOYSA-N 0.000 claims description 6
- 125000001931 aliphatic group Chemical group 0.000 claims description 6
- QQVIHTHCMHWDBS-UHFFFAOYSA-N isophthalic acid Chemical compound OC(=O)C1=CC=CC(C(O)=O)=C1 QQVIHTHCMHWDBS-UHFFFAOYSA-N 0.000 claims description 6
- 229920001169 thermoplastic Polymers 0.000 claims description 6
- 239000004416 thermosoftening plastic Substances 0.000 claims description 6
- 239000012943 hotmelt Substances 0.000 claims description 4
- 229920003002 synthetic resin Polymers 0.000 claims description 4
- 239000000057 synthetic resin Substances 0.000 claims description 4
- 239000000654 additive Substances 0.000 claims description 3
- 229910052799 carbon Inorganic materials 0.000 claims description 3
- 150000001991 dicarboxylic acids Chemical class 0.000 claims description 3
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims description 2
- 239000007787 solid Substances 0.000 claims description 2
- 239000002253 acid Substances 0.000 description 7
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 6
- 239000011888 foil Substances 0.000 description 6
- 239000002904 solvent Substances 0.000 description 6
- 150000007513 acids Chemical class 0.000 description 5
- 239000000539 dimer Substances 0.000 description 5
- 238000004519 manufacturing process Methods 0.000 description 5
- 239000012141 concentrate Substances 0.000 description 4
- NAQMVNRVTILPCV-UHFFFAOYSA-N hexane-1,6-diamine Chemical compound NCCCCCCN NAQMVNRVTILPCV-UHFFFAOYSA-N 0.000 description 4
- 238000012545 processing Methods 0.000 description 4
- 239000001993 wax Substances 0.000 description 4
- 238000011161 development Methods 0.000 description 3
- 230000018109 developmental process Effects 0.000 description 3
- MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 3
- 239000000975 dye Substances 0.000 description 3
- 150000002148 esters Chemical class 0.000 description 3
- RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Substances CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 3
- 238000010438 heat treatment Methods 0.000 description 3
- 239000000123 paper Substances 0.000 description 3
- 239000004033 plastic Substances 0.000 description 3
- 229920003023 plastic Polymers 0.000 description 3
- PUPZLCDOIYMWBV-UHFFFAOYSA-N (+/-)-1,3-Butanediol Chemical compound CC(O)CCO PUPZLCDOIYMWBV-UHFFFAOYSA-N 0.000 description 2
- IANQTJSKSUMEQM-UHFFFAOYSA-N 1-benzofuran Chemical compound C1=CC=C2OC=CC2=C1 IANQTJSKSUMEQM-UHFFFAOYSA-N 0.000 description 2
- YBYIRNPNPLQARY-UHFFFAOYSA-N 1H-indene Chemical compound C1=CC=C2CC=CC2=C1 YBYIRNPNPLQARY-UHFFFAOYSA-N 0.000 description 2
- FALRKNHUBBKYCC-UHFFFAOYSA-N 2-(chloromethyl)pyridine-3-carbonitrile Chemical compound ClCC1=NC=CC=C1C#N FALRKNHUBBKYCC-UHFFFAOYSA-N 0.000 description 2
- HZAXFHJVJLSVMW-UHFFFAOYSA-N 2-Aminoethan-1-ol Chemical compound NCCO HZAXFHJVJLSVMW-UHFFFAOYSA-N 0.000 description 2
- MVDKKZZVTWHVMC-UHFFFAOYSA-N 2-hexadecylpropanedioic acid Chemical class CCCCCCCCCCCCCCCCC(C(O)=O)C(O)=O MVDKKZZVTWHVMC-UHFFFAOYSA-N 0.000 description 2
- RNLHGQLZWXBQNY-UHFFFAOYSA-N 3-(aminomethyl)-3,5,5-trimethylcyclohexan-1-amine Chemical compound CC1(C)CC(N)CC(C)(CN)C1 RNLHGQLZWXBQNY-UHFFFAOYSA-N 0.000 description 2
- YOOSAIJKYCBPFW-UHFFFAOYSA-N 3-[4-(3-aminopropoxy)butoxy]propan-1-amine Chemical compound NCCCOCCCCOCCCN YOOSAIJKYCBPFW-UHFFFAOYSA-N 0.000 description 2
- RSWGJHLUYNHPMX-UHFFFAOYSA-N Abietic-Saeure Natural products C12CCC(C(C)C)=CC2=CCC2C1(C)CCCC2(C)C(O)=O RSWGJHLUYNHPMX-UHFFFAOYSA-N 0.000 description 2
- PIICEJLVQHRZGT-UHFFFAOYSA-N Ethylenediamine Chemical compound NCCN PIICEJLVQHRZGT-UHFFFAOYSA-N 0.000 description 2
- GLUUGHFHXGJENI-UHFFFAOYSA-N Piperazine Chemical compound C1CNCCN1 GLUUGHFHXGJENI-UHFFFAOYSA-N 0.000 description 2
- 239000004952 Polyamide Substances 0.000 description 2
- KHPCPRHQVVSZAH-HUOMCSJISA-N Rosin Natural products O(C/C=C/c1ccccc1)[C@H]1[C@H](O)[C@@H](O)[C@@H](O)[C@@H](CO)O1 KHPCPRHQVVSZAH-HUOMCSJISA-N 0.000 description 2
- UIIMBOGNXHQVGW-UHFFFAOYSA-M Sodium bicarbonate Chemical compound [Na+].OC([O-])=O UIIMBOGNXHQVGW-UHFFFAOYSA-M 0.000 description 2
- WNLRTRBMVRJNCN-UHFFFAOYSA-N adipic acid Chemical compound OC(=O)CCCCC(O)=O WNLRTRBMVRJNCN-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
- WPYMKLBDIGXBTP-UHFFFAOYSA-N benzoic acid Chemical compound OC(=O)C1=CC=CC=C1 WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 description 2
- 238000007664 blowing Methods 0.000 description 2
- 238000009833 condensation Methods 0.000 description 2
- 230000005494 condensation Effects 0.000 description 2
- XBDQKXXYIPTUBI-UHFFFAOYSA-N dimethylselenoniopropionate Natural products CCC(O)=O XBDQKXXYIPTUBI-UHFFFAOYSA-N 0.000 description 2
- GHLKSLMMWAKNBM-UHFFFAOYSA-N dodecane-1,12-diol Chemical compound OCCCCCCCCCCCCO GHLKSLMMWAKNBM-UHFFFAOYSA-N 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 238000007646 gravure printing Methods 0.000 description 2
- 239000000025 natural resin Substances 0.000 description 2
- BDJRBEYXGGNYIS-UHFFFAOYSA-N nonanedioic acid Chemical compound OC(=O)CCCCCCCC(O)=O BDJRBEYXGGNYIS-UHFFFAOYSA-N 0.000 description 2
- FBUKVWPVBMHYJY-UHFFFAOYSA-N nonanoic acid Chemical compound CCCCCCCCC(O)=O FBUKVWPVBMHYJY-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
- WLJVNTCWHIRURA-UHFFFAOYSA-N pimelic acid Chemical compound OC(=O)CCCCCC(O)=O WLJVNTCWHIRURA-UHFFFAOYSA-N 0.000 description 2
- 229920002647 polyamide Polymers 0.000 description 2
- AOHJOMMDDJHIJH-UHFFFAOYSA-N propylenediamine Chemical compound CC(N)CN AOHJOMMDDJHIJH-UHFFFAOYSA-N 0.000 description 2
- CXMXRPHRNRROMY-UHFFFAOYSA-N sebacic acid Chemical compound OC(=O)CCCCCCCCC(O)=O CXMXRPHRNRROMY-UHFFFAOYSA-N 0.000 description 2
- TYFQFVWCELRYAO-UHFFFAOYSA-N suberic acid Chemical compound OC(=O)CCCCCCC(O)=O TYFQFVWCELRYAO-UHFFFAOYSA-N 0.000 description 2
- 239000000758 substrate Substances 0.000 description 2
- 229940014800 succinic anhydride Drugs 0.000 description 2
- KHPCPRHQVVSZAH-UHFFFAOYSA-N trans-cinnamyl beta-D-glucopyranoside Natural products OC1C(O)C(O)C(CO)OC1OCC=CC1=CC=CC=C1 KHPCPRHQVVSZAH-UHFFFAOYSA-N 0.000 description 2
- 238000009736 wetting Methods 0.000 description 2
- MUTGBJKUEZFXGO-OLQVQODUSA-N (3as,7ar)-3a,4,5,6,7,7a-hexahydro-2-benzofuran-1,3-dione Chemical compound C1CCC[C@@H]2C(=O)OC(=O)[C@@H]21 MUTGBJKUEZFXGO-OLQVQODUSA-N 0.000 description 1
- KMOUUZVZFBCRAM-OLQVQODUSA-N (3as,7ar)-3a,4,7,7a-tetrahydro-2-benzofuran-1,3-dione Chemical compound C1C=CC[C@@H]2C(=O)OC(=O)[C@@H]21 KMOUUZVZFBCRAM-OLQVQODUSA-N 0.000 description 1
- SWRRWODUBVHJBC-UHFFFAOYSA-N 1-(2-piperidin-1-ylpropan-2-yl)piperidine Chemical compound N1(CCCCC1)C(C)(C)N1CCCCC1 SWRRWODUBVHJBC-UHFFFAOYSA-N 0.000 description 1
- DPQHRXRAZHNGRU-UHFFFAOYSA-N 2,4,4-trimethylhexane-1,6-diamine Chemical compound NCC(C)CC(C)(C)CCN DPQHRXRAZHNGRU-UHFFFAOYSA-N 0.000 description 1
- GCVQVCAAUXFNGJ-UHFFFAOYSA-N 2-hexadecylbutanedioic acid Chemical class CCCCCCCCCCCCCCCCC(C(O)=O)CC(O)=O GCVQVCAAUXFNGJ-UHFFFAOYSA-N 0.000 description 1
- DMWMTABVCDLUIY-UHFFFAOYSA-N 2-hexadecylpentanedioic acid Chemical class CCCCCCCCCCCCCCCCC(C(O)=O)CCC(O)=O DMWMTABVCDLUIY-UHFFFAOYSA-N 0.000 description 1
- NMOVZJTXSAJASG-UHFFFAOYSA-N 3-[3-(3-aminopropoxy)butoxy]propan-1-amine Chemical compound NCCCOC(C)CCOCCCN NMOVZJTXSAJASG-UHFFFAOYSA-N 0.000 description 1
- KOGSPLLRMRSADR-UHFFFAOYSA-N 4-(2-aminopropan-2-yl)-1-methylcyclohexan-1-amine Chemical compound CC(C)(N)C1CCC(C)(N)CC1 KOGSPLLRMRSADR-UHFFFAOYSA-N 0.000 description 1
- BVUDKBBYMKCBAM-UHFFFAOYSA-N 4-[2-[2-(3-aminopropoxy)ethoxy]ethoxy]butan-1-amine Chemical compound NCCCCOCCOCCOCCCN BVUDKBBYMKCBAM-UHFFFAOYSA-N 0.000 description 1
- BLFRQYKZFKYQLO-UHFFFAOYSA-N 4-aminobutan-1-ol Chemical compound NCCCCO BLFRQYKZFKYQLO-UHFFFAOYSA-N 0.000 description 1
- FFEKEPNLQVJRKO-UHFFFAOYSA-N 5-(5-aminopentoxy)pentan-1-amine Chemical compound NCCCCCOCCCCCN FFEKEPNLQVJRKO-UHFFFAOYSA-N 0.000 description 1
- 239000005711 Benzoic acid Substances 0.000 description 1
- DPUOLQHDNGRHBS-UHFFFAOYSA-N Brassidinsaeure Natural products CCCCCCCCC=CCCCCCCCCCCCC(O)=O DPUOLQHDNGRHBS-UHFFFAOYSA-N 0.000 description 1
- 239000004215 Carbon black (E152) Substances 0.000 description 1
- RPNUMPOLZDHAAY-UHFFFAOYSA-N Diethylenetriamine Chemical compound NCCNCCN RPNUMPOLZDHAAY-UHFFFAOYSA-N 0.000 description 1
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 1
- 229920000877 Melamine resin Polymers 0.000 description 1
- 239000005643 Pelargonic acid Substances 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
- 239000004721 Polyphenylene oxide Substances 0.000 description 1
- 229920001800 Shellac Polymers 0.000 description 1
- 150000001253 acrylic acids Chemical class 0.000 description 1
- 239000001361 adipic acid Substances 0.000 description 1
- 235000011037 adipic acid Nutrition 0.000 description 1
- 150000001335 aliphatic alkanes Chemical class 0.000 description 1
- 150000007933 aliphatic carboxylic acids Chemical class 0.000 description 1
- 125000002947 alkylene group Chemical group 0.000 description 1
- 150000001408 amides Chemical class 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- 238000007098 aminolysis reaction Methods 0.000 description 1
- 239000003963 antioxidant agent Substances 0.000 description 1
- 235000010233 benzoic acid Nutrition 0.000 description 1
- CDQSJQSWAWPGKG-UHFFFAOYSA-N butane-1,1-diol Chemical class CCCC(O)O CDQSJQSWAWPGKG-UHFFFAOYSA-N 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
- 239000003054 catalyst Substances 0.000 description 1
- 229920002678 cellulose Polymers 0.000 description 1
- 239000001913 cellulose Substances 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- YVWBQGFBSVLPIK-UHFFFAOYSA-N cyclohex-2-ene-1-carboxylic acid Chemical compound OC(=O)C1CCCC=C1 YVWBQGFBSVLPIK-UHFFFAOYSA-N 0.000 description 1
- YQLZOAVZWJBZSY-UHFFFAOYSA-N decane-1,10-diamine Chemical compound NCCCCCCCCCCN YQLZOAVZWJBZSY-UHFFFAOYSA-N 0.000 description 1
- 238000006471 dimerization reaction Methods 0.000 description 1
- 238000004821 distillation Methods 0.000 description 1
- QFTYSVGGYOXFRQ-UHFFFAOYSA-N dodecane-1,12-diamine Chemical compound NCCCCCCCCCCCCN QFTYSVGGYOXFRQ-UHFFFAOYSA-N 0.000 description 1
- TVIDDXQYHWJXFK-UHFFFAOYSA-N dodecanedioic acid Chemical compound OC(=O)CCCCCCCCCCC(O)=O TVIDDXQYHWJXFK-UHFFFAOYSA-N 0.000 description 1
- 238000010894 electron beam technology Methods 0.000 description 1
- 230000007613 environmental effect Effects 0.000 description 1
- 238000003912 environmental pollution Methods 0.000 description 1
- FPIQZBQZKBKLEI-UHFFFAOYSA-N ethyl 1-[[2-chloroethyl(nitroso)carbamoyl]amino]cyclohexane-1-carboxylate Chemical compound ClCCN(N=O)C(=O)NC1(C(=O)OCC)CCCCC1 FPIQZBQZKBKLEI-UHFFFAOYSA-N 0.000 description 1
- 125000004494 ethyl ester group Chemical group 0.000 description 1
- 150000002171 ethylene diamines Chemical class 0.000 description 1
- 238000001704 evaporation Methods 0.000 description 1
- 230000008020 evaporation Effects 0.000 description 1
- 238000004880 explosion Methods 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 125000000623 heterocyclic group Chemical group 0.000 description 1
- ACCCMOQWYVYDOT-UHFFFAOYSA-N hexane-1,1-diol Chemical class CCCCCC(O)O ACCCMOQWYVYDOT-UHFFFAOYSA-N 0.000 description 1
- XXMIOPMDWAUFGU-UHFFFAOYSA-N hexane-1,6-diol Chemical compound OCCCCCCO XXMIOPMDWAUFGU-UHFFFAOYSA-N 0.000 description 1
- 230000036571 hydration Effects 0.000 description 1
- 238000006703 hydration reaction Methods 0.000 description 1
- 229930195733 hydrocarbon Natural products 0.000 description 1
- 150000002430 hydrocarbons Chemical class 0.000 description 1
- 238000005984 hydrogenation reaction Methods 0.000 description 1
- 150000002576 ketones Chemical class 0.000 description 1
- 238000004898 kneading Methods 0.000 description 1
- 238000012423 maintenance Methods 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
- FPYJFEHAWHCUMM-UHFFFAOYSA-N maleic anhydride Chemical compound O=C1OC(=O)C=C1 FPYJFEHAWHCUMM-UHFFFAOYSA-N 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- JDSHMPZPIAZGSV-UHFFFAOYSA-N melamine Chemical compound NC1=NC(N)=NC(N)=N1 JDSHMPZPIAZGSV-UHFFFAOYSA-N 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 239000000178 monomer Substances 0.000 description 1
- 239000012170 montan wax Substances 0.000 description 1
- SXJVFQLYZSNZBT-UHFFFAOYSA-N nonane-1,9-diamine Chemical compound NCCCCCCCCCN SXJVFQLYZSNZBT-UHFFFAOYSA-N 0.000 description 1
- 229920003986 novolac Polymers 0.000 description 1
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N phenol group Chemical group C1(=CC=CC=C1)O ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 1
- 229920001568 phenolic resin Polymers 0.000 description 1
- 239000005011 phenolic resin Substances 0.000 description 1
- 239000004014 plasticizer Substances 0.000 description 1
- 229920001225 polyester resin Polymers 0.000 description 1
- 239000004645 polyester resin Substances 0.000 description 1
- 229920000570 polyether Polymers 0.000 description 1
- 229920000098 polyolefin Polymers 0.000 description 1
- 235000020777 polyunsaturated fatty acids Nutrition 0.000 description 1
- 229920002689 polyvinyl acetate Polymers 0.000 description 1
- 239000011118 polyvinyl acetate Substances 0.000 description 1
- 235000019260 propionic acid Nutrition 0.000 description 1
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- KIDHWZJUCRJVML-UHFFFAOYSA-N putrescine Chemical compound NCCCCN KIDHWZJUCRJVML-UHFFFAOYSA-N 0.000 description 1
- IUVKMZGDUIUOCP-BTNSXGMBSA-N quinbolone Chemical compound O([C@H]1CC[C@H]2[C@H]3[C@@H]([C@]4(C=CC(=O)C=C4CC3)C)CC[C@@]21C)C1=CCCC1 IUVKMZGDUIUOCP-BTNSXGMBSA-N 0.000 description 1
- 230000001105 regulatory effect Effects 0.000 description 1
- 239000013557 residual solvent Substances 0.000 description 1
- ZLGIYFNHBLSMPS-ATJNOEHPSA-N shellac Chemical compound OCCCCCC(O)C(O)CCCCCCCC(O)=O.C1C23[C@H](C(O)=O)CCC2[C@](C)(CO)[C@@H]1C(C(O)=O)=C[C@@H]3O ZLGIYFNHBLSMPS-ATJNOEHPSA-N 0.000 description 1
- 239000004208 shellac Substances 0.000 description 1
- 229940113147 shellac Drugs 0.000 description 1
- 235000013874 shellac Nutrition 0.000 description 1
- 229910000030 sodium bicarbonate Inorganic materials 0.000 description 1
- 235000017557 sodium bicarbonate Nutrition 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
- 238000012546 transfer Methods 0.000 description 1
- DXNCZXXFRKPEPY-UHFFFAOYSA-N tridecanedioic acid Chemical compound OC(=O)CCCCCCCCCCCC(O)=O DXNCZXXFRKPEPY-UHFFFAOYSA-N 0.000 description 1
- ZIBGPFATKBEMQZ-UHFFFAOYSA-N triethylene glycol Chemical compound OCCOCCOCCO ZIBGPFATKBEMQZ-UHFFFAOYSA-N 0.000 description 1
- KLNPWTHGTVSSEU-UHFFFAOYSA-N undecane-1,11-diamine Chemical compound NCCCCCCCCCCCN KLNPWTHGTVSSEU-UHFFFAOYSA-N 0.000 description 1
- LWBHHRRTOZQPDM-UHFFFAOYSA-N undecanedioic acid Chemical compound OC(=O)CCCCCCCCCC(O)=O LWBHHRRTOZQPDM-UHFFFAOYSA-N 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 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
- C09D11/00—Inks
- C09D11/02—Printing inks
- C09D11/10—Printing inks based on artificial resins
- C09D11/102—Printing inks based on artificial resins containing macromolecular compounds obtained by reactions other than those only involving unsaturated carbon-to-carbon bonds
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G69/00—Macromolecular compounds obtained by reactions forming a carboxylic amide link in the main chain of the macromolecule
- C08G69/02—Polyamides derived from amino-carboxylic acids or from polyamines and polycarboxylic acids
- C08G69/26—Polyamides derived from amino-carboxylic acids or from polyamines and polycarboxylic acids derived from polyamines and polycarboxylic acids
- C08G69/34—Polyamides derived from amino-carboxylic acids or from polyamines and polycarboxylic acids derived from polyamines and polycarboxylic acids using polymerised unsaturated fatty acids
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G69/00—Macromolecular compounds obtained by reactions forming a carboxylic amide link in the main chain of the macromolecule
- C08G69/44—Polyester-amides
Landscapes
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Wood Science & Technology (AREA)
- Inks, Pencil-Leads, Or Crayons (AREA)
- Polyamides (AREA)
- Printing Methods (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE19752534845 DE2534845A1 (de) | 1975-08-05 | 1975-08-05 | Druckverfahren und dafuer geeignete schmelzdruckfarben |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| NO762703L true NO762703L (fr) | 1977-02-08 |
Family
ID=5953226
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| NO762703A NO762703L (fr) | 1975-08-05 | 1976-08-04 |
Country Status (13)
| Country | Link |
|---|---|
| US (1) | US4066585A (fr) |
| JP (1) | JPS5220106A (fr) |
| BE (1) | BE844916A (fr) |
| DE (1) | DE2534845A1 (fr) |
| DK (1) | DK353476A (fr) |
| ES (1) | ES450465A1 (fr) |
| FR (1) | FR2320189A1 (fr) |
| GB (1) | GB1508253A (fr) |
| IT (1) | IT1065241B (fr) |
| LU (1) | LU75521A1 (fr) |
| NL (1) | NL7608650A (fr) |
| NO (1) | NO762703L (fr) |
| SE (1) | SE7608758L (fr) |
Families Citing this family (64)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
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| DE2942680C2 (de) * | 1979-10-23 | 1986-02-27 | Schering AG, 1000 Berlin und 4709 Bergkamen | Schmelzkleber auf Basis von Polyesteramiden und deren Verwendung zum Verkleben von organischen und anorganischen Substraten |
| FR2471394A1 (fr) * | 1979-12-10 | 1981-06-19 | Rhone Poulenc Ind | Copolyesteramides souples a basse temperature |
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| DE3101243C2 (de) * | 1981-01-16 | 1983-10-13 | Niedermayr Papierwarenfabrik Ag, 8200 Rosenheim | Rotatives Flexo- bzw. indirektes Tiefdruckverfahren, sowie Vorrichtung zur Durchführung des Verfahrens |
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| US4756760A (en) * | 1986-09-15 | 1988-07-12 | Basf Corporation | Drying oil soap for intaglio inks |
| DE3751815T2 (de) * | 1987-06-10 | 1997-01-23 | Kinyosha Kk | Harzhaltige kalanderwalze |
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| DE3918368A1 (de) * | 1989-06-06 | 1990-12-20 | Schering Ag | Polyamidharze auf basis dimerisierter fettsaeuren, verfahren zu ihrer herstellung und verfahren zur herstellung von druckfarben unter mitverwendung der polyamidharze |
| US5151386A (en) * | 1990-08-01 | 1992-09-29 | Mobil Solar Energy Corporation | Method of applying metallized contacts to a solar cell |
| DE4024981A1 (de) * | 1990-08-07 | 1992-02-13 | Schering Ag | Verwendung von polyamidharzen fuer den reliefdruck |
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| DE4205713C2 (de) * | 1992-02-25 | 1994-08-04 | Siegwerk Druckfarben Gmbh & Co | Druckfarbe, Verfahren zu ihrer Herstellung und deren Verwendung |
| US5703145A (en) * | 1993-06-30 | 1997-12-30 | Hitachi Koki Co., Ltd. | Hot melt type ink composition for ink jet |
| US5973025A (en) * | 1994-04-12 | 1999-10-26 | Sri International | Aqueous ink compositions containing a binder of a neutralized acidic resin |
| DE19536679A1 (de) * | 1995-09-30 | 1997-04-10 | Hoechst Ag | Beschichtung in Druckerzeugnissen, bestehend aus mehreren Lagen, und Verfahren zu ihrer Herstellung |
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| JP3797763B2 (ja) * | 1997-09-08 | 2006-07-19 | 富士通テン株式会社 | フラックス組成物 |
| US6063834A (en) * | 1997-12-08 | 2000-05-16 | Lexmark International, Inc. | Wet-rub resistant ink compositions |
| GB2336594A (en) * | 1998-04-21 | 1999-10-27 | Coates Brothers Plc | Radiation-curable Ink Compositions |
| US6444018B1 (en) * | 1998-06-25 | 2002-09-03 | Xerox Corporation | Phase change ink carrier compositions containing anhydride/amino alcohol-based adducts |
| DE19854423A1 (de) * | 1998-11-25 | 2000-05-31 | Cognis Deutschland Gmbh | Feste Druckfarben |
| WO2000058025A1 (fr) * | 1999-03-30 | 2000-10-05 | Cognis Corporation | Compositions a base de resine polyamide resistant a l'abrasion et a l'efflorescence |
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| US6492458B1 (en) | 2000-05-16 | 2002-12-10 | Arizona Chemical Company | Polyalkyleneoxydiamine polyamides useful for formulating inks for phase-change jet printing |
| US6710121B2 (en) * | 2000-05-19 | 2004-03-23 | Arizona Chemical Company | Nitrocellulose-compatible laminating ink resins |
| DE10139822B4 (de) * | 2000-09-06 | 2009-04-02 | Heidelberger Druckmaschinen Ag | Thermografische Druckeinrichtung und thermografisches Druckverfahren |
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| US6399713B1 (en) | 2001-01-24 | 2002-06-04 | Arizona Chemical Company | Hydrocarbon-terminated polyether-polyamide block copolymers and uses thereof |
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| US6552160B2 (en) | 2001-05-14 | 2003-04-22 | Arizona Chemical Company | Ester-terminated poly(ester-amides) useful for formulating transparent gels in low polarity fluids |
| US6841590B2 (en) | 2001-12-28 | 2005-01-11 | Sun Chemical Corporation | Hot melt flexographic inks and method of preparing same |
| US20060183813A1 (en) * | 2001-12-28 | 2006-08-17 | Jitendra Modi | Hot melt coating compositions and methods of preparing same |
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| CN1777631A (zh) * | 2003-02-27 | 2006-05-24 | 史蒂文·W·福克斯 | 芳酰胺聚合物体系及其制备方法 |
| US7786250B2 (en) * | 2003-02-27 | 2010-08-31 | Fowkes Steven W | Vector directional polymer systems and methods of nano-structural self assembly |
| US6960248B2 (en) * | 2003-05-22 | 2005-11-01 | Arizona Chemical Company | Cyclic bisamides useful in formulating inks for phase-change printing |
| US6860930B2 (en) * | 2003-06-25 | 2005-03-01 | Xerox Corporation | Phase change inks containing branched triamides |
| US6946025B2 (en) * | 2003-10-22 | 2005-09-20 | Xerox Corporation | Process for preparing tetra-amide compounds |
| JP4660811B2 (ja) * | 2003-12-15 | 2011-03-30 | ハリマ化成株式会社 | 印刷インキ用ポリアミド樹脂組成物 |
| US6989052B1 (en) * | 2004-06-30 | 2006-01-24 | Xerox Corporation | Phase change ink printing process |
| DE102004056492B3 (de) * | 2004-11-23 | 2006-08-10 | Fraunhofer-Gesellschaft zur Förderung der angewandten Forschung e.V. | Verfahren zum strukturierten Aufbringen einer thermoplastischen Paste auf ein Substrat und dessen Verwendung |
| EP2726564A2 (fr) * | 2011-06-30 | 2014-05-07 | OCE-Technologies B.V. | Composition d'encre thermofusible comprenant un copolyester et procédé pour la préparation d'un copolyester |
| CN103781461A (zh) * | 2011-09-09 | 2014-05-07 | 禾大国际股份公开有限公司 | 用于个人护理的聚酰胺组合物 |
| WO2014104317A1 (fr) * | 2012-12-28 | 2014-07-03 | 花王株式会社 | Liant de pavage |
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| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| NL131829C (fr) * | 1962-03-12 | |||
| US3420789A (en) * | 1962-03-26 | 1969-01-07 | Coates Brothers & Co | Polyamide resins having solubility and resistance to gelling in alcohol solutions |
| US3383391A (en) * | 1963-12-19 | 1968-05-14 | Sun Chemical Corp | Imide terminated polyamide resins useful in inks |
| US3622604A (en) * | 1964-10-15 | 1971-11-23 | Schering Ag | Synthetic polyamides of a dimeric fatty acid, a lower aliphatic carboxylic acid ethylene diamine, and a co-diamine |
| US3461092A (en) * | 1965-08-23 | 1969-08-12 | Owens Illinois Inc | Solid particulate printing ink composition and process for producing same |
| US3522270A (en) * | 1966-08-26 | 1970-07-28 | Gen Mills Inc | Polyamide-polyimide resin |
| US3700618A (en) * | 1969-07-31 | 1972-10-24 | Emery Industries Inc | Polyamides exhibiting improved freezethaw characteristics in printing ink compositions |
| US3639313A (en) * | 1969-11-26 | 1972-02-01 | Sun Chemical Corp | Modified polyamide resins |
| BE755035A (fr) * | 1969-12-02 | 1971-02-01 | Gen Mills Inc | Resine polyamide a base d'acides gras polymeres |
| US3776867A (en) * | 1970-10-05 | 1973-12-04 | Richardson Ink Co | Solventless non-polluting vehicles for heat-set inks |
| JPS4917877B1 (fr) * | 1970-12-29 | 1974-05-04 | ||
| DE2128984A1 (de) * | 1971-06-11 | 1973-01-04 | Schering Ag | Kaschierfaehiges druckfarbenharz auf polyamid-basis |
| US3778394A (en) * | 1972-08-24 | 1973-12-11 | Gen Mills Chem Inc | Polymeric fatty acid polyamide modified with a rosin adduct |
| US3872044A (en) * | 1972-09-25 | 1975-03-18 | Ferro Corp | Thermoplastic screen process inks |
-
1975
- 1975-08-05 DE DE19752534845 patent/DE2534845A1/de active Pending
-
1976
- 1976-08-03 US US05/711,147 patent/US4066585A/en not_active Expired - Lifetime
- 1976-08-03 LU LU75521A patent/LU75521A1/xx unknown
- 1976-08-04 NL NL7608650A patent/NL7608650A/xx not_active Application Discontinuation
- 1976-08-04 ES ES450465A patent/ES450465A1/es not_active Expired
- 1976-08-04 JP JP51093093A patent/JPS5220106A/ja active Pending
- 1976-08-04 NO NO762703A patent/NO762703L/no unknown
- 1976-08-04 IT IT26002/76A patent/IT1065241B/it active
- 1976-08-04 SE SE7608758A patent/SE7608758L/xx unknown
- 1976-08-04 GB GB32484/76A patent/GB1508253A/en not_active Expired
- 1976-08-05 FR FR7623924A patent/FR2320189A1/fr active Granted
- 1976-08-05 BE BE169586A patent/BE844916A/fr unknown
- 1976-08-05 DK DK353476A patent/DK353476A/da unknown
Also Published As
| Publication number | Publication date |
|---|---|
| NL7608650A (nl) | 1977-02-08 |
| BE844916A (fr) | 1977-02-07 |
| DE2534845A1 (de) | 1977-02-10 |
| US4066585A (en) | 1978-01-03 |
| FR2320189A1 (fr) | 1977-03-04 |
| FR2320189B3 (fr) | 1979-05-04 |
| IT1065241B (it) | 1985-02-25 |
| JPS5220106A (en) | 1977-02-15 |
| SE7608758L (sv) | 1977-02-06 |
| ES450465A1 (es) | 1977-08-16 |
| GB1508253A (en) | 1978-04-19 |
| LU75521A1 (fr) | 1977-03-25 |
| DK353476A (da) | 1977-02-06 |
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