EP0119958A1 - Desensitizing ink for wet offset printing - Google Patents
Desensitizing ink for wet offset printing Download PDFInfo
- Publication number
- EP0119958A1 EP0119958A1 EP84810115A EP84810115A EP0119958A1 EP 0119958 A1 EP0119958 A1 EP 0119958A1 EP 84810115 A EP84810115 A EP 84810115A EP 84810115 A EP84810115 A EP 84810115A EP 0119958 A1 EP0119958 A1 EP 0119958A1
- Authority
- EP
- European Patent Office
- Prior art keywords
- alkanoxylated
- ink
- nucleophilic compound
- ink according
- bridged
- Prior art date
- 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.)
- Granted
Links
- 238000007645 offset printing Methods 0.000 title claims abstract description 10
- 150000001875 compounds Chemical class 0.000 claims abstract description 17
- 230000000269 nucleophilic effect Effects 0.000 claims abstract description 17
- 229920000728 polyester Polymers 0.000 claims abstract description 13
- 239000000126 substance Substances 0.000 claims abstract description 7
- 239000004814 polyurethane Substances 0.000 claims abstract 5
- 229920002635 polyurethane Polymers 0.000 claims abstract 5
- 229920001228 polyisocyanate Polymers 0.000 claims abstract 2
- 239000005056 polyisocyanate Substances 0.000 claims abstract 2
- 125000003118 aryl group Chemical group 0.000 claims description 8
- 238000007639 printing Methods 0.000 claims description 8
- 239000002253 acid Substances 0.000 claims description 7
- 125000001931 aliphatic group Chemical group 0.000 claims description 7
- 229920000180 alkyd Polymers 0.000 claims description 7
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 7
- 235000014113 dietary fatty acids Nutrition 0.000 claims description 5
- 229930195729 fatty acid Natural products 0.000 claims description 5
- 239000000194 fatty acid Substances 0.000 claims description 5
- 150000004665 fatty acids Chemical class 0.000 claims description 5
- 239000010685 fatty oil Substances 0.000 claims description 5
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 4
- 239000003921 oil Substances 0.000 claims description 4
- 230000015572 biosynthetic process Effects 0.000 claims description 3
- 238000005809 transesterification reaction Methods 0.000 claims description 2
- 239000000976 ink Substances 0.000 description 33
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 14
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 14
- 239000002966 varnish Substances 0.000 description 9
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 7
- 229910000019 calcium carbonate Inorganic materials 0.000 description 7
- 229910052814 silicon oxide Inorganic materials 0.000 description 7
- 239000004408 titanium dioxide Substances 0.000 description 7
- JOXIMZWYDAKGHI-UHFFFAOYSA-N toluene-4-sulfonic acid Chemical compound CC1=CC=C(S(O)(=O)=O)C=C1 JOXIMZWYDAKGHI-UHFFFAOYSA-N 0.000 description 6
- KXGFMDJXCMQABM-UHFFFAOYSA-N 2-methoxy-6-methylphenol Chemical class [CH]OC1=CC=CC([CH])=C1O KXGFMDJXCMQABM-UHFFFAOYSA-N 0.000 description 5
- 238000000518 rheometry Methods 0.000 description 5
- 238000006243 chemical reaction Methods 0.000 description 4
- 239000005022 packaging material Substances 0.000 description 4
- 229920001451 polypropylene glycol Polymers 0.000 description 4
- 229920005989 resin Polymers 0.000 description 4
- 239000011347 resin Substances 0.000 description 4
- RPNUMPOLZDHAAY-UHFFFAOYSA-N Diethylenetriamine Chemical compound NCCNCCN RPNUMPOLZDHAAY-UHFFFAOYSA-N 0.000 description 3
- 229910052799 carbon Inorganic materials 0.000 description 3
- KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 description 3
- 239000011248 coating agent Substances 0.000 description 3
- 238000000576 coating method Methods 0.000 description 3
- 125000004836 hexamethylene group Chemical group [H]C([H])([*:2])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[*:1] 0.000 description 3
- 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
- 241000209504 Poaceae Species 0.000 description 2
- 239000002202 Polyethylene glycol 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
- KKEYFWRCBNTPAC-UHFFFAOYSA-N Terephthalic acid Chemical compound OC(=O)C1=CC=C(C(O)=O)C=C1 KKEYFWRCBNTPAC-UHFFFAOYSA-N 0.000 description 2
- ZJCCRDAZUWHFQH-UHFFFAOYSA-N Trimethylolpropane Chemical compound CCC(CO)(CO)CO ZJCCRDAZUWHFQH-UHFFFAOYSA-N 0.000 description 2
- JXCHMDATRWUOAP-UHFFFAOYSA-N diisocyanatomethylbenzene Chemical compound O=C=NC(N=C=O)C1=CC=CC=C1 JXCHMDATRWUOAP-UHFFFAOYSA-N 0.000 description 2
- 238000010438 heat treatment Methods 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- 230000007935 neutral effect Effects 0.000 description 2
- 230000003472 neutralizing effect Effects 0.000 description 2
- QQVIHTHCMHWDBS-UHFFFAOYSA-N perisophthalic acid Natural products OC(=O)C1=CC=CC(C(O)=O)=C1 QQVIHTHCMHWDBS-UHFFFAOYSA-N 0.000 description 2
- 229920001515 polyalkylene glycol Polymers 0.000 description 2
- 229920001223 polyethylene glycol Polymers 0.000 description 2
- WBHHMMIMDMUBKC-XLNAKTSKSA-N ricinelaidic acid Chemical compound CCCCCC[C@@H](O)C\C=C\CCCCCCCC(O)=O WBHHMMIMDMUBKC-XLNAKTSKSA-N 0.000 description 2
- 229960003656 ricinoleic acid Drugs 0.000 description 2
- FEUQNCSVHBHROZ-UHFFFAOYSA-N ricinoleic acid Natural products CCCCCCC(O[Si](C)(C)C)CC=CCCCCCCCC(=O)OC FEUQNCSVHBHROZ-UHFFFAOYSA-N 0.000 description 2
- 238000003756 stirring Methods 0.000 description 2
- KDYFGRWQOYBRFD-UHFFFAOYSA-N succinic acid Chemical compound OC(=O)CCC(O)=O KDYFGRWQOYBRFD-UHFFFAOYSA-N 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
- WRIDQFICGBMAFQ-UHFFFAOYSA-N (E)-8-Octadecenoic acid Natural products CCCCCCCCCC=CCCCCCCC(O)=O WRIDQFICGBMAFQ-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
- QSBYPNXLFMSGKH-UHFFFAOYSA-N 9-Heptadecensaeure Natural products CCCCCCCC=CCCCCCCCC(O)=O QSBYPNXLFMSGKH-UHFFFAOYSA-N 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-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
- 239000004359 castor oil Substances 0.000 description 1
- 235000019438 castor oil Nutrition 0.000 description 1
- 239000003054 catalyst Substances 0.000 description 1
- 238000004090 dissolution Methods 0.000 description 1
- 230000008030 elimination Effects 0.000 description 1
- 238000003379 elimination reaction Methods 0.000 description 1
- 239000000839 emulsion Substances 0.000 description 1
- 150000002148 esters Chemical class 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
- 230000002209 hydrophobic effect Effects 0.000 description 1
- QXJSBBXBKPUZAA-UHFFFAOYSA-N isooleic acid Natural products CCCCCCCC=CCCCCCCCCC(O)=O QXJSBBXBKPUZAA-UHFFFAOYSA-N 0.000 description 1
- ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid Chemical compound CCCCCCCC\C=C/CCCCCCCC(O)=O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 description 1
- 230000035939 shock Effects 0.000 description 1
- 239000001384 succinic acid Substances 0.000 description 1
Classifications
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B41—PRINTING; LINING MACHINES; TYPEWRITERS; STAMPS
- B41M—PRINTING, DUPLICATING, MARKING, OR COPYING PROCESSES; COLOUR PRINTING
- B41M5/00—Duplicating or marking methods; Sheet materials for use therein
- B41M5/124—Duplicating or marking methods; Sheet materials for use therein using pressure to make a masked colour visible, e.g. to make a coloured support visible, to create an opaque or transparent pattern, or to form colour by uniting colour-forming components
- B41M5/128—Desensitisers; Compositions for fault correction, detection or identification of the layers
-
- 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]
- Y10T428/31551—Of polyamidoester [polyurethane, polyisocyanate, polycarbamate, etc.]
Definitions
- the subject of the invention is a desensitizing ink for wet offset printing on an acceptor surface of a carbonless chemical assembly, comprising at least two superimposed sheets, the facing faces of which have, one an electrophilic acceptor coating, and the another a nucleophilic coating capable of producing a chromogenic reaction with said accepting electrophilic coating.
- the owner of the present invention has produced a desensitizing ink, based on polyalkylene glycol or other high molecular weight alkanoxylated nucleophilic compounds, making it possible to print the acceptor surface of a set chemical carbonless by wet offset printing, following alkanoxylation to a degree such that their hydrophilic-lipophilic balance (HLB) is between 2 and 9 in order to allow, on the one hand, a continuous transfer of the ink rollers. inkers on the hydrophobic areas of the printing plate moistened with an offset press, and, on the other hand, to neutralize corresponding areas of the acceptor surface of the carbonless chemical assembly.
- HLB hydrophilic-lipophilic balance
- the alkanoxylated nucleophilic compound is bridged by an aliphatic or aromatic polyisocianate derivative or by an aliphatic or aromatic polyacid derivative, which also makes it possible to improve the transfer of the ink onto the inking train of the wet offset press. This also results in an ink flow of constant thickness by the rollers of the inking train.
- This ink film is particularly resistant to the shock resulting from the emulsion of fountain water in the ink before being transferred successively to the offset printing plate, then to the blanket and finally in the form of a layer of desensitizing ink, at a rate of 1.5 to 5 gr / m2, on a paper support.
- a desensitizing ink according to the invention for wet offset printing of the acceptor surface of a carbonless carbon assembly, can be formulated as follows.
- 70 parts of a varnish obtained by reaction of 63 parts of polypropylene glycol (PM 2550) with 5 parts of hexamethylene triisocyanate and addition of 32 parts of acid modified phenolic resin, with 13 parts, are mixed on a three-cylinder grinder. parts of titanium dioxide, 1 part of silicon oxide and 6 parts of calcium carbonate.
- HLB Hydrophilic Lipophilic Balance: 4 [i 1]
- polyester varnish 67 parts are mixed on a 3-cylinder mill with 10 parts of titanium dioxide, 2 parts of silicon oxide, 6 parts of calcium carbonate and 13 parts of liquid citric polyester.
- the ink thus obtained has good neutralizing properties in wet offset (HLB: 4 [ ⁇ 11), a viscosity of 110 poises and an initial draft of 155 units.
- the polyester can be synthesized with an aromatic polyacid such as isophthalic or terephthalic acid.
- polyester from propoxylated diethylene triamine of similar molecular weight.
- part or all of the water required to ensure saturation of these areas can be emulsified in the ink mass.
Landscapes
- Inks, Pencil-Leads, Or Crayons (AREA)
- Color Printing (AREA)
Abstract
Un composé nucléophile alcanoylé est ponté sous forme de polyuréthanne par un dérivé polyisocyanate ou sous forme de polyester par un dérivé polyacide. On obtient ainsi une encre désensibilisante pour impression en offset humide sur une surface acceptrice d'un ensemble autocopiant chimique.An alkanoylated nucleophilic compound is bridged in the form of polyurethane by a polyisocyanate derivative or in the form of polyester by a polyacid derivative. A desensitizing ink for wet offset printing is thus obtained on an acceptor surface of a carbonless chemical assembly.
Description
L'invention a pour objet une encre désensibilisante pour impression en offset humide sur une surface acceptrice d'un ensemble autocopiant chimique, comprenant au-moins deux feuilles superposées dont les faces en regard présentent, l'une un enduit électrophile accepteur, et l'autre un enduit nucléophile susceptible de produire une réaction chromogène avec ledit enduit électrophile accepteur.The subject of the invention is a desensitizing ink for wet offset printing on an acceptor surface of a carbonless chemical assembly, comprising at least two superimposed sheets, the facing faces of which have, one an electrophilic acceptor coating, and the another a nucleophilic coating capable of producing a chromogenic reaction with said accepting electrophilic coating.
Par le brevet anglais N° 1.433-469, on connaît déjà des encres désen- sibilisantes contenant du polypropylène glycol de poids moléculaire compris entre 400 et 5000 permettant d'imprimer en typographie, flexographie ou hélio-. graphie la surface acceptrice d'un ensemble autocopiant et d'empêcher ainsi toute formation colorée dans les zones ainsi imprimées, lors d'une écriture ou frappe subséquente sur l'ensemble autocopiant.For the English Patent No. 1433-469, are already known DESEN inks - sibilisantes containing molecular weight polypropylene glycol of between 400 and 5000 for printing letterpress, flexographic or helio-. prints the acceptor surface of a carbonless assembly and thus prevents any colored formation in the areas thus printed, during a subsequent writing or typing on the carbonless assembly.
Comme indiqué dans le brevet anglais N° 1.525.269, la titulaire du brevet anglais N° 1.433.469 n'avait toutefois pas réussi à formuler une encre à base de polyalkylène glycol permettant d'imprimer en offset humide la surface acceptrice d'un ensemble autocopiant chimique.As indicated in the English patent N ° 1.525.269, the owner of the English patent N ° 1.433.469 had however not succeeded in formulating an ink based on polyalkylene glycol allowing to print in wet offset the acceptor surface of a carbonless chemical assembly.
Comme décrit dans le brevet suisse N° 628.288, la titulaire de la présente invention a réalisé une encre désensibilisante, à base de polyalkylène glycol ou d'autre composés nucléophiles alcanoxylés de poids moléculaire élevé, permettant d'imprimer la surface acceptrice d'un ensemble autocopiant chimique par impression en offset humide, à la suite d'une alcanoxylation à un degré tel que leur équilibre hydrophile-lipophile (HLB) soit compris entre 2 et 9 afin de permettre, d'une part, un transfert continu de l'encre des rouleaux. encreurs sur les zones hydrophobes de la plaque d'impression humidifiée d'une presse offset, et, d'autre part, de neutraliser des zones correspondantes de la surface acceptrice de l'ensemble autocopiant chimique.As described in Swiss Patent No. 628,288, the owner of the present invention has produced a desensitizing ink, based on polyalkylene glycol or other high molecular weight alkanoxylated nucleophilic compounds, making it possible to print the acceptor surface of a set chemical carbonless by wet offset printing, following alkanoxylation to a degree such that their hydrophilic-lipophilic balance (HLB) is between 2 and 9 in order to allow, on the one hand, a continuous transfer of the ink rollers. inkers on the hydrophobic areas of the printing plate moistened with an offset press, and, on the other hand, to neutralize corresponding areas of the acceptor surface of the carbonless chemical assembly.
Afin d'augmenter le poids moléculaire du composant désensibilisant l'encre selon l'invention, est caractérisée en ce que le composé nucléophile alcanoxylé est ponté par un dérivé polyisocianate aliphatique ou aromatique ou encore par un derive polyacide aliphatique ou aromatique, qui permet en plus d'améliorer le transfert de l'encre sur le train d'encrage de la presse offset humide. Il en résulte encore un débit d'encre d'épaisseur constante par les rouleaux du train d'encrage. Ce film d'encre résiste particulièrement bien au choc résultant de l'émulsion de l'eau de mouillage dans l'encre avant d'être transféré successivement sur la plaque d'impression offset, puis sur le blanchet et finalement sous forme d'une couche d'encre désensibilisante, à raison de 1,5 à 5 gr/m2, sur un support de papier.In order to increase the molecular weight of the ink desensitizing component according to the invention, is characterized in that the alkanoxylated nucleophilic compound is bridged by an aliphatic or aromatic polyisocianate derivative or by an aliphatic or aromatic polyacid derivative, which also makes it possible to improve the transfer of the ink onto the inking train of the wet offset press. This also results in an ink flow of constant thickness by the rollers of the inking train. This ink film is particularly resistant to the shock resulting from the emulsion of fountain water in the ink before being transferred successively to the offset printing plate, then to the blanket and finally in the form of a layer of desensitizing ink, at a rate of 1.5 to 5 gr / m2, on a paper support.
Une encre désensibilisante selon l'invention, pour impression en offset humide de la surface acceptrice d'un ensemble autocopiant chimique, peut être formulée de la façon suivante.A desensitizing ink according to the invention, for wet offset printing of the acceptor surface of a carbonless carbon assembly, can be formulated as follows.
On mélange sur une broyeuse à trois cylindres, 70 parties d'un vernis obtenu par réaction de 63 parties de polypropylène-glycol (P.M. 2550) avec 5 parties de triisocyanate d'hexaméthylène et adjonction de 32 parties de résine phénolique modifiée acide, avec 13 parties de dioxyde de titane, 1 partie d'oxyde de silicium et 6 parties de carbonate de calcium.70 parts of a varnish obtained by reaction of 63 parts of polypropylene glycol (PM 2550) with 5 parts of hexamethylene triisocyanate and addition of 32 parts of acid modified phenolic resin, with 13 parts, are mixed on a three-cylinder grinder. parts of titanium dioxide, 1 part of silicon oxide and 6 parts of calcium carbonate.
A cette encre broyée on ajoute 12 parties de dérivé alcanoxylé. La valeur HLB de l'encre s'élève à 3 ( - 1). Cette encre possède une rhéologie adéquate pour l'impression en offset humide.To this ground ink 12 parts of alkanoxylated derivative are added. The HLB value of the ink is 3 (- 1). This ink has a rheology suitable for printing in wet offset.
On mélange sur une broyeuse à trois cylindres, 68 parties d'un vernis obtenu par réaction de 66 parties de diéthylène triamine propoxylé (P.M. 2500) avec 9 parties de triméthylolpropane isocyanuré par 3 moles de di-isocyanate de toluylène et adjonction de 25 parties de résine phénolique modifié acide, avec 12 parties de dioxyde de titane, 2 parties d'oxyde de silicium et 6 parties de carbonate de calcium.68 parts of a varnish obtained by reacting 66 parts of propoxylated diethylene triamine (PM 2500) with 9 parts of trimethylolpropane isocyanated with 3 moles of toluylene diisocyanate and addition of 25 parts of a three-cylinder mill is mixed on a three-cylinder mill acid modified phenolic resin, with 12 parts of titanium dioxide, 2 parts of silicon oxide and 6 parts of calcium carbonate.
A cette encre broyée on ajoute 12 parties de dérivé alcanoxylé. La valeur HLB de l'encre s'élève à 4 ( ±1). Cette encre possède une rhéologie adéquate pour l'impression en offset humide.To this ground ink 12 parts of alkanoxylated derivative are added. The HLB value of the ink is 4 ( ± 1). This ink has a rheology suitable for printing in wet offset.
On mélange sur une broyeuse à trois cylindres, 60 parties d'un vernis obtenu par réaction de 58 parties de polypropylène glycol (P.M. 2500) avec 8 parties d'acide ricinoléique et 10 parties de triméthylolpropane isocyanuré par 3 moles60 parts of a varnish obtained by reaction of 58 parts of polypropylene glycol (P.M. 2500) with 8 parts of ricinoleic acid and 10 parts of isocyanurized trimethylolpropane per 3 moles are mixed on a three-roller mill
de di-isocyanate de toluylène et adjonction de 24 parties de résine de collophane esterifiée neutre, avec 20 parties de dioxyde de titane, 2 parties d'oxyde de silicium et 6 parties de carbonate de calcium.of toluylene diisocyanate and addition of 24 parts of neutral esterified rosin resin, with 20 parts of titanium dioxide, 2 parts of silicon oxide and 6 parts of calcium carbonate.
A cette encre broyée on ajoute 12 parties de dérivé alcanoxylé. La valeur HLB de l'encre s'élève à 3 ( fi). Cette encre possède une rhéologie adéquate pour l'impression en offset humide.To this ground ink 12 parts of alkanoxylated derivative are added. The HLB value of the ink is 3 (fi). This ink has a rheology suitable for printing in wet offset.
On mélange sur une broyeuse à trois cylindres, 60 parties d'un vernis obtenu par réaction de 72 parties de diéthylène triamine propoxylé (P.M. 2500) avec 5 parties d'huile de ricin et 5 parties de tri-isocyanate d'hexaméthylène et adjonction de 18 parties de résine de collophane estérifiée neutre, avec 20 parties de dioxyde de titane, 2 parties d'oxyde de silicium et 6 parties de carbonate de calcium.60 parts of a varnish obtained by reacting 72 parts of propoxylated diethylene triamine (PM 2500) with 5 parts of castor oil and 5 parts of hexamethylene triisocyanate and addition of 18 parts of neutral esterified rosin resin, with 20 parts of titanium dioxide, 2 parts of silicon oxide and 6 parts of calcium carbonate.
A cette encre broyée on ajoute 12 parties de dérivé alcanoxylé. La valeur HLB de l'encre s'élève à 4 (±1). Cette encre possède une rhéologie adéquate pour l'impression en offset humide.To this ground ink 12 parts of alkanoxylated derivative are added. The HLB value of the ink is 4 (± 1). This ink has a rheology suitable for printing in wet offset.
On mélange sur une broyeuse à trois cylindres, 68 parties d'un vernis obtenu par réaction de 75 parties de polypropylène glycol (P.M. 2500) avec 5 parties d'alkyde longue en huile et 5 parties de tri-isocyanate d'hexaméthylène et adjonction de 15 parties de résine phénolique modifiée acide, avec 12 parties de dioxyde de titane, 2 parties d'oxyde de silicium et 6 parties de carbonate de calcium.68 parts of a varnish obtained by reacting 75 parts of polypropylene glycol (PM 2500) with 5 parts of long alkyd in oil and 5 parts of hexamethylene triisocyanate and addition of 15 parts of acid modified phenolic resin, with 12 parts of titanium dioxide, 2 parts of silicon oxide and 6 parts of calcium carbonate.
A cette encre broyée on ajoute 12 parties de dérivé alcanoxylé. La valeur HLB de l'encre s'élève à 3 ( ± 1). Cette encre possède une rhéologie adéquate pour l'impression en offset humide.To this ground ink 12 parts of alkanoxylated derivative are added. The HLB value of the ink is 3 (± 1). This ink has a rheology suitable for printing in wet offset.
Dans l'encre désensibilisante telle que formulée aux exemples 3, 4 et 5 on a substitué soit un acide gras porteur de groupes hydroxyles (exemple 3), soit une huile grasse (exemple 4) soit un alkyde long en huile (exemple 5) à une partie du composé mucléophile alcanoxylé, ce qui permet d'augmenter la viscosité de l'encre.In the desensitizing ink as formulated in Examples 3, 4 and 5, either a fatty acid carrying hydroxyl groups (Example 3) or a fatty oil (Example 4) or a long oil alkyd (Example 5) has been substituted for part of the alkanoxylated muclophilic compound, which makes it possible to increase the viscosity of the ink.
Au dérivé alcanoxylé qui peut s'écrire HO (R) OH on peut ajouter une quantité stoechiométrique de diacide. En présence d'acide p-toluène-sulfonique en tant que catalyseur on obtient ainsi un polyester. Comme la température de réaction est supérieure à 100°C, la formation d'ester s'accompagne d'élimination d'eau récupérable dans une colonne Dean-Starke. Le produit augmente de poids moléculaire qui se traduit par une augmentation de viscosité.To the alkanoxylated derivative which can be written HO (R) OH, a stoichiometric amount of diacid can be added. In the presence of p-toluenesulfonic acid as a catalyst, a polyester is thus obtained. As the reaction temperature is above 100 ° C, the formation of ester is accompanied by elimination nation of recoverable water in a Dean-Starke column. The product increases in molecular weight which results in an increase in viscosity.
On fait réagir à une température supérieure à 100°C et en présence de 0,2 parties d'acide p-toluène-sulfonique, 96 parties de polyèthylène glycol avec 4 parties d'acide succinique et on obtient le polyester succinique. A 65 parties de polyester succinique on ajoute sous agitation 35 parties de résine phénolique modifiée acide, puis on chauffe jusqu'à dissolution complète de la résine. Le vernis ainsi obtenu possède une vicosité de 120 poises (mesuré à 25°C sur viscosimètre cône-plaque de Haake).Reacted at a temperature above 100 ° C and in the presence of 0.2 parts of p-toluene sulfonic acid, 96 parts of polyethylene glycol with 4 parts of succinic acid and the polyester succinic is obtained. To 65 parts of succinic polyester is added with stirring 35 parts of acid modified phenolic resin, then heating until complete dissolution of the resin. The varnish thus obtained has a viscosity of 120 poises (measured at 25 ° C. on a Haake cone-plate viscometer).
-On mélange sur une broyeuse à 3 cylindres, 70 parties de ce vernis polyester avec 10 parties de dioxyde de titane, 2 parties d'oxyde de silicium, 6 parties de carbonate de calcium et 10 parties de polyester succinique liquide.- 70 parts of this polyester varnish are mixed on a 3-cylinder grinder with 10 parts of titanium dioxide, 2 parts of silicon oxide, 6 parts of calcium carbonate and 10 parts of liquid succinic polyester.
L'encre ainsi obtenue présente de bonne propriétés neutralisantes, un bon équilibre eau/encre (HLB=Hydrophilic Lipophilic Balance: 4 [i 1]), une viscosité de 120 poises, un tirant initial de 150 unités (mesuré sur Tack-OScope de Test- print à une vitesse de 100 m/min. à 25°C) et un bon transfert sur le train d'encrage.The ink thus obtained has good neutralizing properties, a good water / ink balance (HLB = Hydrophilic Lipophilic Balance: 4 [i 1]), a viscosity of 120 poises, an initial draft of 150 units (measured on Tack-OScope of Test-print at a speed of 100 m / min at 25 ° C) and good transfer to the inking train.
On fait réagir à une température supérieure à 100°C et en présence de 0,2 parties d'acide p-toluène-sulfonique, 94 parties de polyéthylène glycol avec 6 parties d'acide citrique et on obtient le polyester citrique.Reacted at a temperature above 100 ° C and in the presence of 0.2 parts of p-toluene sulfonic acid, 94 parts of polyethylene glycol with 6 parts of citric acid and the citric polyester is obtained.
A 68 parties de polyester citrique on ajoute sous agitation 38 parties de résine phénolique modifiée acide, puis on chauffe jusqu'à dissolution complète de la résine. Le vernis ainsi obtenu possède une viscosité de 140 poises à 25°C.To 68 parts of citric polyester 38 parts of acid modified phenolic resin are added with stirring, then heating until the resin is completely dissolved. The varnish thus obtained has a viscosity of 140 poises at 25 ° C.
On mélange sur une broyeuse à 3 cylindres, 67 parties de vernis polyester avec 10 parties de dioxyde de titane, 2 parties d'oxyde de silicium, 6 parties de carbonate de calcium et 13 parties de polyester citrique liquide.67 parts of polyester varnish are mixed on a 3-cylinder mill with 10 parts of titanium dioxide, 2 parts of silicon oxide, 6 parts of calcium carbonate and 13 parts of liquid citric polyester.
L'encre ainsi obtenue présente de bonnes propriétés neutralisantes en offset humide (HLB: 4 [± 11), une viscosité de 110 poises et un tirant initial de 155 unités.The ink thus obtained has good neutralizing properties in wet offset (HLB: 4 [± 11), a viscosity of 110 poises and an initial draft of 155 units.
Selon une variante, on peut faire la synthese du polyester avec un polyacide aromatique tel que l'acide isophtalique ou téréphtalique.Alternatively, the polyester can be synthesized with an aromatic polyacid such as isophthalic or terephthalic acid.
Selon une autre variante, on peut faire la synthèse de polyester à partir de diéthylène triamine propoxylée de poids moléculaire analogue.According to another variant, it is possible to synthesize polyester from propoxylated diethylene triamine of similar molecular weight.
On peut encore substituer une partie du polyacide aliphatique ou aromatique par :
- - soit des acides gras tels que l'acide ricinoléique, l'acide oléique, etc.
- - soit des huiles grasse qui réagissent vers 250°C par transestérification,
- - soit avec les alkydes grasses porteuses de groupes acides.
- - or fatty acids such as ricinoleic acid, oleic acid, etc.
- - or fatty oils which react around 250 ° C by transesterification,
- - either with fatty alkyds carrying acid groups.
Afin de rendre l'humidification des zones hydrophiles de la plaque 'd'impression en offset humide plus aisée, on peut émulsionner dans la masse d'encre une partie ou la totalité de l'eau requise pour assurer la saturation de ces zones.In order to make the moistening of the hydrophilic areas of the wet offset printing plate easier, part or all of the water required to ensure saturation of these areas can be emulsified in the ink mass.
Claims (13)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CH1443/83A CH653049A5 (en) | 1983-03-16 | 1983-03-16 | DESENSITIZING INK FOR WET OFFSET PRINTING. |
| CH1443/83 | 1983-03-16 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| EP0119958A1 true EP0119958A1 (en) | 1984-09-26 |
| EP0119958B1 EP0119958B1 (en) | 1989-05-24 |
Family
ID=4210579
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| EP84810115A Expired EP0119958B1 (en) | 1983-03-16 | 1984-03-07 | Desensitizing ink for wet offset printing |
Country Status (9)
| Country | Link |
|---|---|
| US (1) | US4599111A (en) |
| EP (1) | EP0119958B1 (en) |
| JP (1) | JPS60500759A (en) |
| AU (1) | AU568854B2 (en) |
| CA (1) | CA1216388A (en) |
| CH (1) | CH653049A5 (en) |
| DE (1) | DE3478293D1 (en) |
| PH (1) | PH20466A (en) |
| WO (1) | WO1984003663A1 (en) |
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP0333645A1 (en) * | 1988-02-16 | 1989-09-20 | Sicpa Holding S.A. | Desensitising ink for a chemical-duplicating sheet |
| JP2008529823A (en) * | 2004-12-09 | 2008-08-07 | シクパ・ホールディング・ソシエテ・アノニム | Security element with a viewing angle dependent appearance |
Families Citing this family (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4988563A (en) * | 1988-05-10 | 1991-01-29 | Wehr Mary A | Thermal transfer ribbon with protective layer |
| DE4105767C1 (en) * | 1991-02-23 | 1992-05-27 | Drescher Geschaeftsdrucke Gmbh, 7255 Rutesheim, De | |
| CN104364225A (en) * | 2012-06-06 | 2015-02-18 | 格雷斯公司 | Polyurethane-based waterproofing composition for the water-proofing of concrete structures |
Citations (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB2032932A (en) * | 1978-09-30 | 1980-05-14 | Mitsubishi Paper Mills Ltd | Carbonless pressure sensitive copying paper and a desensitizing ink composition therefor |
Family Cites Families (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS551919B2 (en) * | 1973-08-08 | 1980-01-17 | ||
| JPS5163710A (en) * | 1974-11-26 | 1976-06-02 | Fuji Photo Film Co Ltd |
-
1983
- 1983-03-16 CH CH1443/83A patent/CH653049A5/en not_active IP Right Cessation
-
1984
- 1984-03-07 EP EP84810115A patent/EP0119958B1/en not_active Expired
- 1984-03-07 DE DE8484810115T patent/DE3478293D1/en not_active Expired
- 1984-03-07 CA CA000449033A patent/CA1216388A/en not_active Expired
- 1984-03-12 US US06/668,379 patent/US4599111A/en not_active Expired - Lifetime
- 1984-03-12 JP JP59501826A patent/JPS60500759A/en active Pending
- 1984-03-12 WO PCT/EP1984/000122 patent/WO1984003663A1/en unknown
- 1984-03-12 AU AU28635/84A patent/AU568854B2/en not_active Expired
- 1984-03-15 PH PH30402A patent/PH20466A/en unknown
Patent Citations (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB2032932A (en) * | 1978-09-30 | 1980-05-14 | Mitsubishi Paper Mills Ltd | Carbonless pressure sensitive copying paper and a desensitizing ink composition therefor |
Non-Patent Citations (3)
| Title |
|---|
| CHEMICAL ABSTRACTS, vol. 97, no. 26, 27 décembre 1982, page 784, no. 227562m, Columbus, Ohio, US; & JP-A-57 075 894 (TOYO INK MFG. CO., LTD.) 12-05-1982 82 * |
| PATENT ABSTRACTS OF JAPAN, vol. 6, no. 65 (M-124)[943], 24 avril 1982; & JP-A-57 004 793 (TOYO INK SEIZO K.K.) 11-01-1982 * |
| PATENT ABSTRACTS OF JAPAN, vol. 6, no. 89 (M-132)[967], 27 mai 1982; & JP-A-57 025 991 (TOYO INK SEIZO K.K.) 10-02-1982 * |
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP0333645A1 (en) * | 1988-02-16 | 1989-09-20 | Sicpa Holding S.A. | Desensitising ink for a chemical-duplicating sheet |
| JP2008529823A (en) * | 2004-12-09 | 2008-08-07 | シクパ・ホールディング・ソシエテ・アノニム | Security element with a viewing angle dependent appearance |
| US8211531B2 (en) | 2004-12-09 | 2012-07-03 | Sicpa Holding Sa | Security element having a viewing-angel dependent aspect |
Also Published As
| Publication number | Publication date |
|---|---|
| EP0119958B1 (en) | 1989-05-24 |
| CH653049A5 (en) | 1985-12-13 |
| AU568854B2 (en) | 1988-01-14 |
| US4599111A (en) | 1986-07-08 |
| DE3478293D1 (en) | 1989-06-29 |
| AU2863584A (en) | 1984-10-09 |
| PH20466A (en) | 1987-01-14 |
| JPS60500759A (en) | 1985-05-23 |
| CA1216388A (en) | 1987-01-06 |
| WO1984003663A1 (en) | 1984-09-27 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| US4401470A (en) | Intaglio printing ink and method of employing the same | |
| US4193806A (en) | Viscosity increasing additive for printing inks | |
| US4056453A (en) | Uv-curing printing inks | |
| US4627876A (en) | Printing ink | |
| JP2002012831A (en) | Coating for ink jet printing medium | |
| EP0119958A1 (en) | Desensitizing ink for wet offset printing | |
| JPS62277420A (en) | Urethane modified rosin ester | |
| DE2624674A1 (en) | FLAT PRINT INKS | |
| EP0037477A2 (en) | Copying system and method for its manufacture, and offset or printing dyes useful in this system | |
| US4654082A (en) | Antioxidant gravure printing inks and process of employing the same | |
| EP0088466A1 (en) | Desensitizing ink for emulsion lithographic printing | |
| US5000092A (en) | Printing processes | |
| EP0333645B1 (en) | Desensitising ink for a chemical-duplicating sheet | |
| FR2554013A1 (en) | POLYETHYLENE-OXY GROUP STABLE EMULSIFIER AND SUCCINIC ANHYDRIDE COMPOSITION SUBSTITUTE CONTAINING THE SAME | |
| DE2512285A1 (en) | METHOD OF DESENSITIZATION USING A DESENSITIZING MASS | |
| US4990185A (en) | Lithographic ink compositions | |
| US3427967A (en) | Method of printing with low condensate printing ink | |
| US6265481B1 (en) | Rapidly absorbed printing inks and their use | |
| US2824812A (en) | Hectograph composition | |
| FI64626B (en) | FOERFARANDE FOER FOERSNABBNING AV TORKNING AV OFFSET-TRYCKFAERGER | |
| CH628288A5 (en) | PROCESS FOR DESENSITIZING AN ACCEPTING SURFACE OF A CHEMICAL SELF-COPYING ASSEMBLY. | |
| DE2651100B2 (en) | Printing ink | |
| EP0027804A1 (en) | Printing inks | |
| SU1350044A1 (en) | Method of lithography without wetting | |
| SU926136A1 (en) | Book binding material |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| PUAI | Public reference made under article 153(3) epc to a published international application that has entered the european phase |
Free format text: ORIGINAL CODE: 0009012 |
|
| AK | Designated contracting states |
Designated state(s): BE DE FR GB IT SE |
|
| 17P | Request for examination filed |
Effective date: 19850301 |
|
| 17Q | First examination report despatched |
Effective date: 19860311 |
|
| GRAA | (expected) grant |
Free format text: ORIGINAL CODE: 0009210 |
|
| AK | Designated contracting states |
Kind code of ref document: B1 Designated state(s): BE DE FR GB IT SE |
|
| ITF | It: translation for a ep patent filed |
Owner name: JACOBACCI & PERANI S.P.A. |
|
| GBT | Gb: translation of ep patent filed (gb section 77(6)(a)/1977) | ||
| REF | Corresponds to: |
Ref document number: 3478293 Country of ref document: DE Date of ref document: 19890629 |
|
| PLBE | No opposition filed within time limit |
Free format text: ORIGINAL CODE: 0009261 |
|
| STAA | Information on the status of an ep patent application or granted ep patent |
Free format text: STATUS: NO OPPOSITION FILED WITHIN TIME LIMIT |
|
| 26N | No opposition filed | ||
| ITTA | It: last paid annual fee | ||
| EAL | Se: european patent in force in sweden |
Ref document number: 84810115.0 |
|
| REG | Reference to a national code |
Ref country code: GB Ref legal event code: IF02 |
|
| PGFP | Annual fee paid to national office [announced via postgrant information from national office to epo] |
Ref country code: FR Payment date: 20030217 Year of fee payment: 20 |
|
| PGFP | Annual fee paid to national office [announced via postgrant information from national office to epo] |
Ref country code: GB Payment date: 20030305 Year of fee payment: 20 Ref country code: BE Payment date: 20030305 Year of fee payment: 20 |
|
| PGFP | Annual fee paid to national office [announced via postgrant information from national office to epo] |
Ref country code: SE Payment date: 20030318 Year of fee payment: 20 |
|
| PGFP | Annual fee paid to national office [announced via postgrant information from national office to epo] |
Ref country code: DE Payment date: 20030521 Year of fee payment: 20 |
|
| PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: GB Free format text: LAPSE BECAUSE OF EXPIRATION OF PROTECTION Effective date: 20040306 |
|
| BE20 | Be: patent expired |
Owner name: S.A. *SICPA HOLDING Effective date: 20040307 |
|
| REG | Reference to a national code |
Ref country code: GB Ref legal event code: PE20 |
|
| EUG | Se: european patent has lapsed |