CA1115871A - Methode de preparation d'encres de lithographie a l'epreuve des coulures - Google Patents

Methode de preparation d'encres de lithographie a l'epreuve des coulures

Info

Publication number: CA1115871A
Authority: CA; Canada
Prior art keywords: carbon atoms; pigment; formula; aliphatic; amide
Prior art date: 1977-08-15
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.): Expired

Application number

CA309,088A

Other languages

English (en)

Inventor

Manohar L. Arora

Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)

BASF Corp

Original Assignee

BASF Wyandotte 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.)

1977-08-15

Filing date

1978-08-10

Publication date

1982-01-05

1978-08-10 Application filed by BASF Wyandotte Corp filed Critical BASF Wyandotte Corp

1982-01-05 Application granted granted Critical

1982-01-05 Publication of CA1115871A publication Critical patent/CA1115871A/fr

Status Expired legal-status Critical Current

Links

238000000034 method Methods 0.000 title claims description 30
239000000976 ink Substances 0.000 title description 30
239000000203 mixture Substances 0.000 claims abstract description 21
150000001412 amines Chemical class 0.000 claims abstract description 20
150000001408 amides Chemical class 0.000 claims abstract description 17
239000000080 wetting agent Substances 0.000 claims abstract description 17
239000001054 red pigment Substances 0.000 claims abstract description 7
150000001413 amino acids Chemical class 0.000 claims abstract description 6
WYNCHZVNFNFDNH-UHFFFAOYSA-N Oxazolidine Chemical compound C1COCN1 WYNCHZVNFNFDNH-UHFFFAOYSA-N 0.000 claims abstract description 5
150000001409 amidines Chemical class 0.000 claims abstract description 4
150000002923 oximes Chemical class 0.000 claims abstract description 4
SFZULDYEOVSIKM-UHFFFAOYSA-N chembl321317 Chemical compound C1=CC(C(=N)NO)=CC=C1C1=CC=C(C=2C=CC(=CC=2)C(=N)NO)O1 SFZULDYEOVSIKM-UHFFFAOYSA-N 0.000 claims abstract description 3
238000002156 mixing Methods 0.000 claims abstract description 3
239000000049 pigment Substances 0.000 claims description 60
125000004432 carbon atom Chemical group C* 0.000 claims description 41
125000001931 aliphatic group Chemical group 0.000 claims description 28
-1 pentaerythritol ester Chemical class 0.000 claims description 17
150000003839 salts Chemical class 0.000 claims description 12
239000003981 vehicle Substances 0.000 claims description 11
125000000217 alkyl group Chemical group 0.000 claims description 9
239000006185 dispersion Substances 0.000 claims description 8
RSWGJHLUYNHPMX-UHFFFAOYSA-N Abietic-Saeure Natural products C12CCC(C(C)C)=CC2=CCC2C1(C)CCCC2(C)C(O)=O RSWGJHLUYNHPMX-UHFFFAOYSA-N 0.000 claims description 6
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 claims description 6
229920000768 polyamine Polymers 0.000 claims description 6
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 claims description 6
239000000944 linseed oil Substances 0.000 claims description 5
235000021388 linseed oil Nutrition 0.000 claims description 5
JVVXZOOGOGPDRZ-SLFFLAALSA-N [(1R,4aS,10aR)-1,4a-dimethyl-7-propan-2-yl-2,3,4,9,10,10a-hexahydrophenanthren-1-yl]methanamine Chemical compound NC[C@]1(C)CCC[C@]2(C)C3=CC=C(C(C)C)C=C3CC[C@H]21 JVVXZOOGOGPDRZ-SLFFLAALSA-N 0.000 claims description 4
PAYRUJLWNCNPSJ-UHFFFAOYSA-N N-phenyl amine Natural products NC1=CC=CC=C1 PAYRUJLWNCNPSJ-UHFFFAOYSA-N 0.000 claims description 3
REYJJPSVUYRZGE-UHFFFAOYSA-N Octadecylamine Chemical group CCCCCCCCCCCCCCCCCCN REYJJPSVUYRZGE-UHFFFAOYSA-N 0.000 claims description 3
125000002947 alkylene group Chemical group 0.000 claims description 3
125000003118 aryl group Chemical group 0.000 claims description 3
229910052739 hydrogen Inorganic materials 0.000 claims description 3
239000001257 hydrogen Substances 0.000 claims description 3
125000004435 hydrogen atom Chemical class [H]* 0.000 claims description 3
239000003209 petroleum derivative Substances 0.000 claims description 3
RUFPHBVGCFYCNW-UHFFFAOYSA-N 1-naphthylamine Chemical class C1=CC=C2C(N)=CC=CC2=C1 RUFPHBVGCFYCNW-UHFFFAOYSA-N 0.000 claims description 2
239000003513 alkali Substances 0.000 claims description 2
125000003277 amino group Chemical group 0.000 claims description 2
125000004103 aminoalkyl group Chemical group 0.000 claims description 2
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 2
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 2
ISWSIDIOOBJBQZ-UHFFFAOYSA-N phenol group Chemical group C1(=CC=CC=C1)O ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 claims description 2
229920000058 polyacrylate Polymers 0.000 claims description 2
239000002383 tung oil Substances 0.000 claims description 2
125000002490 anilino group Chemical class [H]N(*)C1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 claims 1
125000000160 oxazolidinyl group Chemical group 0.000 claims 1
239000000243 solution Substances 0.000 description 16
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 10
230000000740 bleeding effect Effects 0.000 description 9
239000011248 coating agent Substances 0.000 description 9
238000000576 coating method Methods 0.000 description 9
229920005989 resin Polymers 0.000 description 6
239000011347 resin Substances 0.000 description 6
238000011282 treatment Methods 0.000 description 6
LYRFLYHAGKPMFH-UHFFFAOYSA-N octadecanamide Chemical class CCCCCCCCCCCCCCCCCC(N)=O LYRFLYHAGKPMFH-UHFFFAOYSA-N 0.000 description 5
150000001448 anilines Chemical class 0.000 description 4
239000003795 chemical substances by application Substances 0.000 description 4
239000003921 oil Substances 0.000 description 4
235000019198 oils Nutrition 0.000 description 4
239000000047 product Substances 0.000 description 4
239000002904 solvent Substances 0.000 description 4
239000002966 varnish Substances 0.000 description 4
KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 3
239000002253 acid Substances 0.000 description 3
230000002378 acidificating effect Effects 0.000 description 3
150000001875 compounds Chemical class 0.000 description 3
235000014113 dietary fatty acids Nutrition 0.000 description 3
238000001035 drying Methods 0.000 description 3
239000000194 fatty acid Substances 0.000 description 3
229930195729 fatty acid Natural products 0.000 description 3
150000004665 fatty acids Chemical class 0.000 description 3
238000011010 flushing procedure Methods 0.000 description 3
229920006270 hydrocarbon resin Polymers 0.000 description 3
125000001183 hydrocarbyl group Chemical group 0.000 description 3
239000012071 phase Substances 0.000 description 3
125000001424 substituent group Chemical group 0.000 description 3
239000001993 wax Substances 0.000 description 3
239000001052 yellow pigment Substances 0.000 description 3
239000004215 Carbon black (E152) Substances 0.000 description 2
QUSNBJAOOMFDIB-UHFFFAOYSA-N Ethylamine Chemical compound CCN QUSNBJAOOMFDIB-UHFFFAOYSA-N 0.000 description 2
239000013032 Hydrocarbon resin Substances 0.000 description 2
VPWFPZBFBFHIIL-UHFFFAOYSA-L Lithol Rubine Chemical compound OC=1C(=CC2=CC=CC=C2C1N=NC1=C(C=C(C=C1)C)S(=O)(=O)[O-])C(=O)[O-].[Na+].[Na+] VPWFPZBFBFHIIL-UHFFFAOYSA-L 0.000 description 2
NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 2
239000004698 Polyethylene Substances 0.000 description 2
150000007513 acids Chemical class 0.000 description 2
239000000654 additive Substances 0.000 description 2
230000001476 alcoholic effect Effects 0.000 description 2
150000001336 alkenes Chemical class 0.000 description 2
239000003963 antioxidant agent Substances 0.000 description 2
235000006708 antioxidants Nutrition 0.000 description 2
239000007900 aqueous suspension Substances 0.000 description 2
HQABUPZFAYXKJW-UHFFFAOYSA-N butan-1-amine Chemical compound CCCCN HQABUPZFAYXKJW-UHFFFAOYSA-N 0.000 description 2
150000004985 diamines Chemical class 0.000 description 2
POULHZVOKOAJMA-UHFFFAOYSA-N dodecanoic acid Chemical compound CCCCCCCCCCCC(O)=O POULHZVOKOAJMA-UHFFFAOYSA-N 0.000 description 2
JRBPAEWTRLWTQC-UHFFFAOYSA-N dodecylamine Chemical compound CCCCCCCCCCCCN JRBPAEWTRLWTQC-UHFFFAOYSA-N 0.000 description 2
230000000694 effects Effects 0.000 description 2
238000005530 etching Methods 0.000 description 2
125000001301 ethoxy group Chemical group [H]C([H])([H])C([H])([H])O* 0.000 description 2
XXUJMEYKYHETBZ-UHFFFAOYSA-N ethyl 4-nitrophenyl ethylphosphonate Chemical compound CCOP(=O)(CC)OC1=CC=C([N+]([O-])=O)C=C1 XXUJMEYKYHETBZ-UHFFFAOYSA-N 0.000 description 2
239000000706 filtrate Substances 0.000 description 2
238000001914 filtration Methods 0.000 description 2
229930195733 hydrocarbon Natural products 0.000 description 2
150000002430 hydrocarbons Chemical class 0.000 description 2
230000002209 hydrophobic effect Effects 0.000 description 2
150000002462 imidazolines Chemical class 0.000 description 2
235000010187 litholrubine BK Nutrition 0.000 description 2
239000000463 material Substances 0.000 description 2
LQNUZADURLCDLV-UHFFFAOYSA-N nitrobenzene Chemical compound [O-][N+](=O)C1=CC=CC=C1 LQNUZADURLCDLV-UHFFFAOYSA-N 0.000 description 2
ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid Chemical compound CCCCCCCC\C=C/CCCCCCCC(O)=O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 description 2
239000005012 oleoresinous Substances 0.000 description 2
239000002245 particle Substances 0.000 description 2
229920000573 polyethylene Polymers 0.000 description 2
150000003141 primary amines Chemical class 0.000 description 2
AOJFQRQNPXYVLM-UHFFFAOYSA-N pyridin-1-ium;chloride Chemical compound [Cl-].C1=CC=[NH+]C=C1 AOJFQRQNPXYVLM-UHFFFAOYSA-N 0.000 description 2
229940037312 stearamide Drugs 0.000 description 2
239000004094 surface-active agent Substances 0.000 description 2
WRIDQFICGBMAFQ-UHFFFAOYSA-N (E)-8-Octadecenoic acid Natural products CCCCCCCCCC=CCCCCCCC(O)=O WRIDQFICGBMAFQ-UHFFFAOYSA-N 0.000 description 1
GAXDEROCNMZYCS-QXMHVHEDSA-N (z)-n,n-dimethyloctadec-9-enamide Chemical compound CCCCCCCC\C=C/CCCCCCCC(=O)N(C)C GAXDEROCNMZYCS-QXMHVHEDSA-N 0.000 description 1
VILCJCGEZXAXTO-UHFFFAOYSA-N 2,2,2-tetramine Chemical compound NCCNCCNCCN VILCJCGEZXAXTO-UHFFFAOYSA-N 0.000 description 1
VGVRFARTWVJNQC-UHFFFAOYSA-N 2-(2,4-dichlorophenoxy)acetamide Chemical compound NC(=O)COC1=CC=C(Cl)C=C1Cl VGVRFARTWVJNQC-UHFFFAOYSA-N 0.000 description 1
TWJNQYPJQDRXPH-UHFFFAOYSA-N 2-cyanobenzohydrazide Chemical compound NNC(=O)C1=CC=CC=C1C#N TWJNQYPJQDRXPH-UHFFFAOYSA-N 0.000 description 1
LQJBNNIYVWPHFW-UHFFFAOYSA-N 20:1omega9c fatty acid Natural products CCCCCCCCCCC=CCCCCCCCC(O)=O LQJBNNIYVWPHFW-UHFFFAOYSA-N 0.000 description 1
IYHIFXGFKVJNBB-UHFFFAOYSA-N 5-chloro-2-[(2-hydroxynaphthalen-1-yl)diazenyl]-4-methylbenzenesulfonic acid Chemical compound C1=C(Cl)C(C)=CC(N=NC=2C3=CC=CC=C3C=CC=2O)=C1S(O)(=O)=O IYHIFXGFKVJNBB-UHFFFAOYSA-N 0.000 description 1
QSBYPNXLFMSGKH-UHFFFAOYSA-N 9-Heptadecensaeure Natural products CCCCCCCC=CCCCCCCCC(O)=O QSBYPNXLFMSGKH-UHFFFAOYSA-N 0.000 description 1
244000215068 Acacia senegal Species 0.000 description 1
NLZUEZXRPGMBCV-UHFFFAOYSA-N Butylhydroxytoluene Chemical compound CC1=CC(C(C)(C)C)=C(O)C(C(C)(C)C)=C1 NLZUEZXRPGMBCV-UHFFFAOYSA-N 0.000 description 1
OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical group [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
241001561902 Chaetodon citrinellus Species 0.000 description 1
MHZGKXUYDGKKIU-UHFFFAOYSA-N Decylamine Chemical compound CCCCCCCCCCN MHZGKXUYDGKKIU-UHFFFAOYSA-N 0.000 description 1
SNRUBQQJIBEYMU-UHFFFAOYSA-N Dodecane Natural products CCCCCCCCCCCC SNRUBQQJIBEYMU-UHFFFAOYSA-N 0.000 description 1
229920000084 Gum arabic Polymers 0.000 description 1
241000692870 Inachis io Species 0.000 description 1
239000005639 Lauric acid Substances 0.000 description 1
PWHULOQIROXLJO-UHFFFAOYSA-N Manganese Chemical compound [Mn] PWHULOQIROXLJO-UHFFFAOYSA-N 0.000 description 1
101100005514 Mus musculus Ccdc40 gene Proteins 0.000 description 1
235000021360 Myristic acid Nutrition 0.000 description 1
TUNFSRHWOTWDNC-UHFFFAOYSA-N Myristic acid Natural products CCCCCCCCCCCCCC(O)=O TUNFSRHWOTWDNC-UHFFFAOYSA-N 0.000 description 1
BACYUWVYYTXETD-UHFFFAOYSA-N N-Lauroylsarcosine Chemical compound CCCCCCCCCCCC(=O)N(C)CC(O)=O BACYUWVYYTXETD-UHFFFAOYSA-N 0.000 description 1
STEVSDAHHBNTQD-UHFFFAOYSA-N N-Methyl-hexadecansaeureamid Natural products CCCCCCCCCCCCCCCC(=O)NC STEVSDAHHBNTQD-UHFFFAOYSA-N 0.000 description 1
239000005642 Oleic acid Substances 0.000 description 1
ZQPPMHVWECSIRJ-UHFFFAOYSA-N Oleic acid Natural products CCCCCCCCC=CCCCCCCCC(O)=O ZQPPMHVWECSIRJ-UHFFFAOYSA-N 0.000 description 1
MBHRHUJRKGNOKX-UHFFFAOYSA-N [(4,6-diamino-1,3,5-triazin-2-yl)amino]methanol Chemical class NC1=NC(N)=NC(NCO)=N1 MBHRHUJRKGNOKX-UHFFFAOYSA-N 0.000 description 1
239000002250 absorbent Substances 0.000 description 1
239000000205 acacia gum Substances 0.000 description 1
235000010489 acacia gum Nutrition 0.000 description 1
239000003929 acidic solution Substances 0.000 description 1
150000007933 aliphatic carboxylic acids Chemical class 0.000 description 1
150000001338 aliphatic hydrocarbons Chemical class 0.000 description 1
230000002152 alkylating effect Effects 0.000 description 1
229910000147 aluminium phosphate Inorganic materials 0.000 description 1
229940124277 aminobutyric acid Drugs 0.000 description 1
230000003078 antioxidant effect Effects 0.000 description 1
239000012736 aqueous medium Substances 0.000 description 1
239000008346 aqueous phase Substances 0.000 description 1
239000007864 aqueous solution Substances 0.000 description 1
IRERQBUNZFJFGC-UHFFFAOYSA-L azure blue Chemical compound [Na+].[Na+].[Na+].[Na+].[Na+].[Na+].[Na+].[Na+].[Al+3].[Al+3].[Al+3].[Al+3].[Al+3].[Al+3].[S-]S[S-].[O-][Si]([O-])([O-])[O-].[O-][Si]([O-])([O-])[O-].[O-][Si]([O-])([O-])[O-].[O-][Si]([O-])([O-])[O-].[O-][Si]([O-])([O-])[O-].[O-][Si]([O-])([O-])[O-] IRERQBUNZFJFGC-UHFFFAOYSA-L 0.000 description 1
239000011230 binding agent Substances 0.000 description 1
239000001055 blue pigment Substances 0.000 description 1
159000000007 calcium salts Chemical class 0.000 description 1
150000001721 carbon Chemical group 0.000 description 1
125000002091 cationic group Chemical group 0.000 description 1
ZLFVRXUOSPRRKQ-UHFFFAOYSA-N chembl2138372 Chemical compound [O-][N+](=O)C1=CC(C)=CC=C1N=NC1=C(O)C=CC2=CC=CC=C12 ZLFVRXUOSPRRKQ-UHFFFAOYSA-N 0.000 description 1
239000008199 coating composition Substances 0.000 description 1
239000013068 control sample Substances 0.000 description 1
238000000354 decomposition reaction Methods 0.000 description 1
230000008021 deposition Effects 0.000 description 1
125000000664 diazo group Chemical group [N-]=[N+]=[*] 0.000 description 1
ZBCBWPMODOFKDW-UHFFFAOYSA-N diethanolamine Chemical class OCCNCCO ZBCBWPMODOFKDW-UHFFFAOYSA-N 0.000 description 1
PQZTVWVYCLIIJY-UHFFFAOYSA-N diethyl(propyl)amine Chemical compound CCCN(CC)CC PQZTVWVYCLIIJY-UHFFFAOYSA-N 0.000 description 1
239000000539 dimer Substances 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
125000005066 dodecenyl group Chemical group C(=CCCCCCCCCCC)* 0.000 description 1
125000003438 dodecyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
229910001651 emery Inorganic materials 0.000 description 1
238000004945 emulsification Methods 0.000 description 1
150000002148 esters Chemical class 0.000 description 1
238000005189 flocculation Methods 0.000 description 1
230000016615 flocculation Effects 0.000 description 1
238000009472 formulation Methods 0.000 description 1
239000012458 free base Substances 0.000 description 1
BTCSSZJGUNDROE-UHFFFAOYSA-N gamma-aminobutyric acid Chemical compound NCCCC(O)=O BTCSSZJGUNDROE-UHFFFAOYSA-N 0.000 description 1
238000010438 heat treatment Methods 0.000 description 1
MTNDZQHUAFNZQY-UHFFFAOYSA-N imidazoline Chemical compound C1CN=CN1 MTNDZQHUAFNZQY-UHFFFAOYSA-N 0.000 description 1
239000004615 ingredient Substances 0.000 description 1
QXJSBBXBKPUZAA-UHFFFAOYSA-N isooleic acid Natural products CCCCCCCC=CCCCCCCCCC(O)=O QXJSBBXBKPUZAA-UHFFFAOYSA-N 0.000 description 1
JJWLVOIRVHMVIS-UHFFFAOYSA-N isopropylamine Chemical compound CC(C)N JJWLVOIRVHMVIS-UHFFFAOYSA-N 0.000 description 1
238000011068 loading method Methods 0.000 description 1
229910052748 manganese Inorganic materials 0.000 description 1
239000011572 manganese Substances 0.000 description 1
KFIGICHILYTCJF-UHFFFAOYSA-N n'-methylethane-1,2-diamine Chemical compound CNCCN KFIGICHILYTCJF-UHFFFAOYSA-N 0.000 description 1
MNOIOAHRVYPSPE-UHFFFAOYSA-N n,n-diethyloctadecan-1-amine Chemical compound CCCCCCCCCCCCCCCCCCN(CC)CC MNOIOAHRVYPSPE-UHFFFAOYSA-N 0.000 description 1
YWFWDNVOPHGWMX-UHFFFAOYSA-N n,n-dimethyldodecan-1-amine Chemical compound CCCCCCCCCCCCN(C)C YWFWDNVOPHGWMX-UHFFFAOYSA-N 0.000 description 1
URMJLBKGJTXVGC-UHFFFAOYSA-N n-dodecylpropanamide Chemical compound CCCCCCCCCCCCNC(=O)CC URMJLBKGJTXVGC-UHFFFAOYSA-N 0.000 description 1
NOSILEXHUBACKG-UHFFFAOYSA-N n-octadecylacetamide Chemical compound CCCCCCCCCCCCCCCCCCNC(C)=O NOSILEXHUBACKG-UHFFFAOYSA-N 0.000 description 1
150000005002 naphthylamines Chemical class 0.000 description 1
239000000025 natural resin Substances 0.000 description 1
150000005181 nitrobenzenes Chemical class 0.000 description 1
229910052757 nitrogen Inorganic materials 0.000 description 1
125000004433 nitrogen atom Chemical group N* 0.000 description 1
JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 description 1
FATBGEAMYMYZAF-UHFFFAOYSA-N oleicacidamide-heptaglycolether Natural products CCCCCCCCC=CCCCCCCCC(N)=O FATBGEAMYMYZAF-UHFFFAOYSA-N 0.000 description 1
239000012860 organic pigment Substances 0.000 description 1
239000003960 organic solvent Substances 0.000 description 1
150000002917 oxazolidines Chemical class 0.000 description 1
WOTPFVNWMLFMFW-ISLYRVAYSA-N para red Chemical class OC1=CC=C2C=CC=CC2=C1\N=N\C1=CC=C(N(=O)=O)C=C1 WOTPFVNWMLFMFW-ISLYRVAYSA-N 0.000 description 1
WXZMFSXDPGVJKK-UHFFFAOYSA-N pentaerythritol Chemical class OCC(CO)(CO)CO WXZMFSXDPGVJKK-UHFFFAOYSA-N 0.000 description 1
DOIRQSBPFJWKBE-UHFFFAOYSA-N phthalic acid di-n-butyl ester Natural products CCCCOC(=O)C1=CC=CC=C1C(=O)OCCCC DOIRQSBPFJWKBE-UHFFFAOYSA-N 0.000 description 1
238000001556 precipitation Methods 0.000 description 1
239000002243 precursor Substances 0.000 description 1
150000003856 quaternary ammonium compounds Chemical class 0.000 description 1
150000003242 quaternary ammonium salts Chemical class 0.000 description 1
239000005871 repellent Substances 0.000 description 1
239000011342 resin composition Substances 0.000 description 1
108700004121 sarkosyl Proteins 0.000 description 1
229940016590 sarkosyl Drugs 0.000 description 1
229920006395 saturated elastomer Polymers 0.000 description 1
150000003335 secondary amines Chemical class 0.000 description 1
239000002002 slurry Substances 0.000 description 1
VVNRQZDDMYBBJY-UHFFFAOYSA-M sodium 1-[(1-sulfonaphthalen-2-yl)diazenyl]naphthalen-2-olate Chemical compound [Na+].C1=CC=CC2=C(S([O-])(=O)=O)C(N=NC3=C4C=CC=CC4=CC=C3O)=CC=C21 VVNRQZDDMYBBJY-UHFFFAOYSA-M 0.000 description 1
239000007787 solid Substances 0.000 description 1
239000000126 substance Substances 0.000 description 1
239000003760 tallow Substances 0.000 description 1
150000003510 tertiary aliphatic amines Chemical class 0.000 description 1
150000003512 tertiary amines Chemical class 0.000 description 1
229920001169 thermoplastic Polymers 0.000 description 1
239000004634 thermosetting polymer Substances 0.000 description 1
239000004416 thermosoftening plastic Substances 0.000 description 1
229960001124 trientine Drugs 0.000 description 1
235000013799 ultramarine blue Nutrition 0.000 description 1
238000005406 washing Methods 0.000 description 1
238000005303 weighing Methods 0.000 description 1
238000009736 wetting Methods 0.000 description 1
239000002023 wood 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
- C09D11/00—Inks
- C09D11/02—Printing inks
- C09D11/03—Printing inks characterised by features other than the chemical nature of the binder

Landscapes

Chemical & Material Sciences (AREA)
Chemical Kinetics & Catalysis (AREA)
General Chemical & Material Sciences (AREA)
Life Sciences & Earth Sciences (AREA)
Engineering & Computer Science (AREA)
Materials Engineering (AREA)
Wood Science & Technology (AREA)
Organic Chemistry (AREA)
Inks, Pencil-Leads, Or Crayons (AREA)
Paints Or Removers (AREA)

CA309,088A 1977-08-15 1978-08-10 Methode de preparation d'encres de lithographie a l'epreuve des coulures Expired CA1115871A (fr)

Applications Claiming Priority (4)

Application Number	Priority Date	Filing Date
US82426477A	1977-08-15	1977-08-15
US824,264		1977-08-15
US83544177A	1977-09-21	1977-09-21
US835,441		1977-09-21

Publications (1)

Publication Number	Publication Date
CA1115871A true CA1115871A (fr)	1982-01-05

Family

ID=27124792

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
CA309,088A Expired CA1115871A (fr)	1977-08-15	1978-08-10	Methode de preparation d'encres de lithographie a l'epreuve des coulures

Country Status (7)

Country	Link
JP (1)	JPS5444908A (fr)
CA (1)	CA1115871A (fr)
DE (1)	DE2835650A1 (fr)
DK (1)	DK358378A (fr)
FR (1)	FR2400543A1 (fr)
GB (1)	GB2002797B (fr)
IT (1)	IT7850737A0 (fr)

Families Citing this family (5)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
JPS60115673A (ja) *	1983-11-25	1985-06-22	Mitsubishi Pencil Co Ltd	油性インク
JP2584580B2 (ja) *	1993-04-30	1997-02-26	株式会社大一商会	パチンコ機の管理装置
JP2641154B2 (ja) *	1995-06-07	1997-08-13	株式会社ソフィア	パチンコ遊技店の集中管理装置
JP2688741B2 (ja) *	1996-04-24	1997-12-10	株式会社ソフィア	データ集計装置
US5922123A (en) *	1997-12-17	1999-07-13	Bayer Corporation	Method for conditioning organic pigments

1978
- 1978-08-10 CA CA309,088A patent/CA1115871A/fr not_active Expired
- 1978-08-11 FR FR7823689A patent/FR2400543A1/fr active Granted
- 1978-08-14 DE DE19782835650 patent/DE2835650A1/de not_active Withdrawn
- 1978-08-14 IT IT7850737A patent/IT7850737A0/it unknown
- 1978-08-14 DK DK358378A patent/DK358378A/da unknown
- 1978-08-15 JP JP9942778A patent/JPS5444908A/ja active Pending
- 1978-08-15 GB GB7833328A patent/GB2002797B/en not_active Expired

Also Published As

Publication number	Publication date
GB2002797B (en)	1982-04-07
JPS5444908A (en)	1979-04-09
IT7850737A0 (it)	1978-08-14
FR2400543A1 (fr)	1979-03-16
GB2002797A (en)	1979-02-28
FR2400543B3 (fr)	1981-05-22
DK358378A (da)	1979-02-16
DE2835650A1 (de)	1979-03-01

Legal Events

Date	Code	Title	Description
1999-01-05	MKEX	Expiry

Publication	Publication Date	Title
CA1115872A (fr)	1982-01-05	Methode de preparation d'encres de lithographie a l'epreuve des coulures
CA2079847C (fr)	1998-01-06	Agents stabilisateurs pour compositions de revetement aqueuses
CA1134980A (fr)	1982-11-02	Encres d'imprimerie et mode d'emploi
AU647917B2 (en)	1994-03-31	Low rub printing ink
US4963188A (en)	1990-10-16	Novel water-based ink composition
US5389130A (en)	1995-02-14	Printing ink emulsion having reduced VOC
EP0285359B1 (fr)	1993-12-15	Encres d'imprimerie
NZ298988A (en)	1999-10-28	Aqueous ink composition comprising water and modified carbon products having an organic carbon group directly attached to the carbon
US5182326A (en)	1993-01-26	Rosin and fatty acid based pigment grinding aids for water-based ink formulations
JPH09100431A (ja)	1997-04-15	大豆油ベース凹版インキ及びその製法
CA1115871A (fr)	1982-01-05	Methode de preparation d'encres de lithographie a l'epreuve des coulures
US4462833A (en)	1984-07-31	Process for treating diarylide yellow pigment
EP0761769B1 (fr)	2002-04-17	Compositions de pigments
US5124412A (en)	1992-06-23	Block copolymer from carboxy terminated polyamide and polyol
US5137568A (en)	1992-08-11	Organokaolin pigments in ink formulations
US3375123A (en)	1968-03-26	Pigment preparations
CA2062824C (fr)	2001-01-23	Encre d'imprimerie anti-voltige
US5306342A (en)	1994-04-26	Production of pigments
WO2005066294A1 (fr)	2005-07-21	Encres lithographiques lavables a l'eau a faible teneur en composes organiques volatils
EP0967256A1 (fr)	1999-12-29	Encre en émulsion pour l'impression par stencil
GB2055878A (en)	1981-03-11	Process for treating azo pigments
US6841592B2 (en)	2005-01-11	Waterfastness additives for aqueous jet inks
US7674327B2 (en)	2010-03-09	Flexographic ink compositions
JP3251644B2 (ja)	2002-01-28	減感インキ
EP0473450A2 (fr)	1992-03-04	Liant résineux à dilution améliorée