EP0119958A1 - Desensitizing ink for wet offset printing - Google Patents

Desensitizing ink for wet offset printing Download PDF

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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
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EP
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Prior art keywords
alkanoxylated
ink
nucleophilic compound
ink according
bridged
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EP84810115A
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German (de)
French (fr)
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EP0119958B1 (en
Inventor
Albert Amon
Roger Weil
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SICPA Holding SA
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SICPA Holding SA
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    • BPERFORMING OPERATIONS; TRANSPORTING
    • B41PRINTING; LINING MACHINES; TYPEWRITERS; STAMPS
    • B41MPRINTING, DUPLICATING, MARKING, OR COPYING PROCESSES; COLOUR PRINTING
    • B41M5/00Duplicating or marking methods; Sheet materials for use therein
    • B41M5/124Duplicating 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
    • B41M5/128Desensitisers; Compositions for fault correction, detection or identification of the layers
    • YGENERAL 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
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10TTECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T428/00Stock material or miscellaneous articles
    • Y10T428/31504Composite [nonstructural laminate]
    • Y10T428/31551Of 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.

Exemple 1Example 1

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.

Exemple 2Example 2

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.

Exemple 3Example 3

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.

Exemple 4Example 4

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.

Exemple 5Example 5

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.

Exemple 6Example 6

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.

Exemple 7Example 7

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.
It is also possible to substitute part of the aliphatic or aromatic polyacid by:
  • - 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)

1. Encre désensibilisante pour impression en offset humide sur une surface acceptrice d'un ensemble autocopiant chimique, comprenant un composé nucléophile alcanoxylé caractérisée en ce que le composé nucléophile alcanoxylé est ponté de façon à augmenter son poids moléculaire et améliorer le transfert de l'encre sur le train d'encrage.1. Desensitizing ink for wet offset printing on an acceptor surface of a carbonless chemical assembly, comprising an alkanoxylated nucleophilic compound characterized in that the alkanoxylated nucleophilic compound is bridged so as to increase its molecular weight and improve the transfer of ink on the inking train. 2. Encre selon la revendication 1, caractérisée en ce que le composé nucléophile alcanoxylé est ponté sous forme de polyuréthane par un dérivé polyisocyanate aliphatique ou aromatique.2. Ink according to claim 1, characterized in that the alkanoxylated nucleophilic compound is bridged in the form of polyurethane by an aliphatic or aromatic polyisocyanate derivative. 3. Encre selon la revendication 1, caractérisée en ce que le composé nucléophile alcanoxylé est ponté sous forme de polyester par un dérivé polyacide.3. Ink according to claim 1, characterized in that the alkanoxylated nucleophilic compound is bridged in the form of polyester by a polyacid derivative. 4. Encre selon la revendication 1, caractérisée en ce qu'elle contient de l'eau émulsionnée dans la masse d'encre.4. Ink according to claim 1, characterized in that it contains water emulsified in the ink mass. 5. Encre selon les revendications 1 et 4, caractérisée en ce que la quantité d'eau émulsionnée dans la masse d'encre est suffisante pour humidifier partiellement les zones hydrophiles d'une plaque d'impression en offset humide.5. Ink according to claims 1 and 4, characterized in that the amount of water emulsified in the ink mass is sufficient to partially moisten the hydrophilic areas of a wet offset printing plate. 6. Encre selon les revendications 1 et 4, caractérisée en ce que la quantité d'eau émulsionnée dans la masse d'encre est suffisante pour assurer une saturation optimale des zones hydrophiles d'une plaque d'impression en offset humide.6. Ink according to claims 1 and 4, characterized in that the amount of water emulsified in the ink mass is sufficient to ensure optimal saturation of the hydrophilic areas of a printing plate in wet offset. 7. Encre selon les revendications 1 et 2, caractérisée en ce qu'une partie du composé nucléophile alcanoxylé est substitué par un acide gras porteur d'au-moins un groupe OH, le composé nucléophile alcanoxylé et l'acide gras étant pontés sous forme de polyuréthane par un dérivé polyisocianate aliphatique ou aromatique.7. Ink according to claims 1 and 2, characterized in that a part of the alkanoxylated nucleophilic compound is substituted by a fatty acid carrying at least one OH group, the alkanoxylated nucleophilic compound and the fatty acid being bridged in the form polyurethane by an aliphatic or aromatic polyisocianate derivative. 8. Encre selon les revendications 1 et 2, caractérisée en ce qu'une partie du composé nucléophile alcanoxylé est substitué par de l'huile grasse porteuse d'au-moins un groupe OH, le composé nucléophile alcanoxylé et l'huile grasse étant pontés sous forme de polyuréthane par un dérivé polyisocianate aliphatique ou aromatique.8. Ink according to claims 1 and 2, characterized in that a part of the alkanoxylated nucleophilic compound is substituted by fatty oil carrying at least one OH group, the alkanoxylated nucleophilic compound and the fatty oil being bridged in the form of polyurethane by an aliphatic or aromatic polyisocianate derivative. 9. Encre selon les revendications 1 et 2, caractérisée en ce qu'une partie du composé nucléophile alcanoxylé est substitué par une alkyde longue en huile porteuse d'au-moins un groupe OH, le composé nucléophile alcanoxylé et l'alkyde longue en huile étant pontés sous forme de polyuréthane par un dérivé polyisocianate aliphatique ou aromatique.9. Ink according to claims 1 and 2, characterized in that a part of the alkanoxylated nucleophilic compound is substituted by a long oil alkyd carrying at least one OH group, the alkanoxylated nucleophilic compound and the long alkyd in oil being bridged in the form of polyurethane by an aliphatic or aromatic polyisocianate derivative. 10. Encre selon les revendications 1 et 3, caractérisée en ce que le composé nucléophile alcanoxylé est ponté par un dérivé polyacide et un acide gras.10. Ink according to claims 1 and 3, characterized in that the alkanoxylated nucleophilic compound is bridged by a polyacid derivative and a fatty acid. 11. Encre selon les revendications 1 et 3, caractérisée en ce que le composé nucléophile alcanoxylé est ponté par un dérivé polyacide et une huile grasse réagissant par transestérification.11. Ink according to claims 1 and 3, characterized in that the alkanoxylated nucleophilic compound is bridged by a polyacid derivative and a fatty oil reacting by transesterification. 12. Encre selon les revendications 1 et 3, caractérisée en ce que le composé nucléophile alcanoxylé est ponté par un dérivé polyacide et une alkyde grasse porteuse de groupes acides.12. Ink according to claims 1 and 3, characterized in that the alkanoxylated nucleophilic compound is bridged by a polyacid derivative and a fatty alkyd carrying acid groups. 13. Utilisation de l'encre selon l'une des revendications 2 à 12 pour l'impression en offset humide de la surface acceptrice d'un ensemble autocopiant chimique pour empêcher toute formation colorée dans les zones ainsi imprimées lors d'une écriture ou frappe subséquente sur l'ensemble autocopiant.13. Use of the ink according to one of claims 2 to 12 for the wet offset printing of the acceptor surface of a chemical carbonless assembly to prevent any colored formation in the areas thus printed during writing or typing. subsequent on the carbonless assembly.
EP84810115A 1983-03-16 1984-03-07 Desensitizing ink for wet offset printing Expired EP0119958B1 (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
CH1443/83 1983-03-16
CH1443/83A CH653049A5 (en) 1983-03-16 1983-03-16 DESENSITIZING INK FOR WET OFFSET PRINTING.

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EP0119958A1 true EP0119958A1 (en) 1984-09-26
EP0119958B1 EP0119958B1 (en) 1989-05-24

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EP84810115A Expired EP0119958B1 (en) 1983-03-16 1984-03-07 Desensitizing ink for wet offset printing

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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)

* Cited by examiner, † Cited by third party
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)

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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
KR20150020540A (en) * 2012-06-06 2015-02-26 더블유.알. 그레이스 앤드 캄파니-콘. Polyurethnae-based waterproofing composition for the water-proofing of concrete structures

Citations (1)

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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

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JPS551919B2 (en) * 1973-08-08 1980-01-17
JPS5163710A (en) * 1974-11-26 1976-06-02 Fuji Photo Film Co Ltd

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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)

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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)

* Cited by examiner, † Cited by third party
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
AU568854B2 (en) 1988-01-14
US4599111A (en) 1986-07-08
JPS60500759A (en) 1985-05-23
DE3478293D1 (en) 1989-06-29
CA1216388A (en) 1987-01-06
WO1984003663A1 (en) 1984-09-27
AU2863584A (en) 1984-10-09
PH20466A (en) 1987-01-14
CH653049A5 (en) 1985-12-13

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