Security document printing ink.

FIELD OF THE INVENTION

This invention belongs to the field of printing inks. More specifically, it is related to printing inks con­taining volatile substances and which are to be used in the method of engraved steel die printing for the print­ing of security documents such as checks, shares, air­line tickets, banknotes, etc.

DESCRIPTION OF THE PRIOR ART

Security documents need to be printed. The printings must be of outstanding high quality and be safe against falsification and counterfeiting.

Security documents are generally printed by a special intaglio printing process. The term "intaglio printing", as a general term, comprises the use of printing ink carrying surfaces, typically printing cylinders or printing plates, where the pattern to be printed is engraved and the engravings are filled with printing ink to be transferred to the printing substrate in order to create the document. The term "intaglio printing" as used in this application shall only define as the engra­ved steel die printing process where chromium plated, engraved steel or nickel plates or cylinders are used, and shall not include the well known rotogravure or gravure printing process.

Furthermore this invention does not relate to low vis­cous printing inks for the conventional gravure printing where a totally different concept of ink formulation is necessary. It is rather related to printing inks in paste form for engraved steel die printing.

In engraved steel die rotary printing, a rotating engra­ved steel cylinder is supplied with ink by one ore more template inking cylinders by which a pattern of inks of different colour is transferred to the printing cylinder. Any excess of ink on the plain surface of the printing cylinder is then wiped off by a rotating wiper cylinder covered by a plastisol, using diluted aqueous sodium hydroxyde as an emulsifying medium for the wiped-off ex­cess ink, or a paper/calico wiping device. Then, the printing pattern in the engravings of the printing cylinder is transferred, under a pressure up to about 500 bars, on the substrate to be printed which may be paper or plastic material in sheet or web form. These steps and the machines used for engraved steel die printing are known in the art.

The main requirements for printing inks to be used to print security documents by the engraved steel die method on modern, presently used sheet fed presses or web machinery are the following: - correct rheological properties at the moment of ink transfer to the printing cylinder and at the moment of printing. - The ability of the excess ink to be easely and quantitatively removed from the non printing areas of the die surface by a PVC-plastisol or rubber wiping cylinder (wipeability). - The ease of cleaning the wiping cylinder by means of a solution of 0.1 to 1 % of caustic soda in water or even pure water (detergability); - Stability of the ink on the inking rollers and until the moment of printing: this means the control of the evaporation of volatile matter during the printing process. - Film forming characteristics allowing further manipulation of sheets or webs carrying printed films of up to 200 microns thickness 24 hours after printing or respectively immediately after printing. - Non-offseting properties: In case of web printing with hot air drying devi­ces (as supplied e.g. from TEC-Systems, W.R. Grace & Co.) web speeds of up to 150 m/min., when using engravings of up to 200 microns, have to be assured. On sheet fed presses 500 to 10,000 sheets, de­pending on printing substrate and depth of en­graving, have to be stackable in piles right after printing without interleaving; - outstanding chemical and mechanical resistance of the printing according to specifications estab­lished by INTERPOL at the 5th International Con­ference on Currency and Counterfeiting in 1969 or the Bureau of Engraving and Printing test methods as stated in BEP-88-214 (TN) section M5.

Typically, a conventional engraved steel die printing ink for security documents has the following composi­tion, all percentages being by weight and referring to the total of the inks: <tables id="tabl0001" num="0001"><img file="EP0340163A2_D0001.tif" /></tables> and polymerization initiators, curing agents and other auxiliary agents in minor amounts.

The applicant has actively been involved in the creation and manufacturing of the above mentioned materials dur­ing the last 20 years. For instance, the move from the so called "trichloroethylene wiping intaglio printing inks" for the engraved steel die printing press to the "waterwiping technology" using intaglio inks which can easily be removed from the PVC wiping roller with a so­lution containing 1% NaOH and 1% sulfonated castor oil, was prepared and strongly influenced by the Assignee Sicpa SA. This change allowed to abandon the use of high­ly toxic solvents such as chlorinated hydrocarbons and has to be considered as a major advancement in the pro­tection of environment.

The volatile organic solvents used are typically mixtu­res of mineral oils (hydrocarbons) having a boiling range of from about 180^o to about 300^oC, and low molecu­lar glycol ethers.

It has already been tried to reduce the concentration of volatile organic substances in the printing ink for en­graved die printing. Thus, U.S. Patent No. 4,764,215 (Rudolph) suggests to incorporate into a conventional water-wipe intaglio ink a drying oil soap, namely the combination of a metal hydroxide, a hydroxyamine such as triethanol amine, and a drying oil. Although the only Example for the manufacture of such a drying oil soap does not disclose a metal hydroxide, it is believed that the drying oil soaps are metal soaps of unsaturated fatty acids stabilized against micelle formation by the hydroxyamine. It is certain that these soaps are low mo­lecular compounds or compositions.

Though such soaps may be effective in allowing the re­duction of the hydrocarbon solvents content of the prin­ting inks, Applicant has found that they do not allow a stable incorporation of even very low amounts of water. Furthermore, printing inks which contain said drying oil soaps in amounts of from 10 to 60 % by weight, with or without reduction of the solvents content, do not suffi­ciently dry after printing, even not after a ten day's period. The inks are not resistant against the action of alkali, and the general resistance or fastness proper­ties are not acceptable.

There is therefore still a need for printing inks having reduced solvent contents but which behave the same as more solvent containing inks or even better.

OBJECTS OF THE INVENTION

In most countries, the Environmental Protection Laws do no longer permit the use of most of organic solvents.

In the printing industry, solvents can often not or not fully be recovered from the exhaust air streams which are emitted from the printing/dryer installations. En­vironmental air and also the air in the printing houses are thus contaminated by solvent vapours. The solvents typically used in engraved steel die printing such as high-boiling mineral oils, glycol ethers, etc., are con­sidered to be dangerous for the human health.

Therefore, there is a first and major object of this in­vention to provide engraved steel die printing inks wherein the amount of the organic solvents is drastical­ly reduced and optionally replaced in part or totally by water.

Another object of the invention is to provide engraved steel die printing inks which do not contain more than about 15% and even less than 12% by weight of volatile organic solvents.

Still another object of this invention is to provide en­graved steel die printing inks for the printing of secu­rity documents which fulfill all requirements regarding the processability and the printing results which are characteristic for organic solvent-based inks.

Another object of the invention is to provide engraved steel die printing inks which can perfectly be emulsi­fied in even weaker solutions of caustic soda or even in pure water.

A further object of the invention is to provide engraved steel die printing inks which can easily be wiped off a chromium plated nickel cylinder or plate at low tempera­tures by means of a plastisol wiping cylinder or a pa­per/calico wiping device. Still another object of the invention is to provide engraved steel die printing inks which give better non-offsetting properties on sheet fed presses allowing to increase the number of sheets stack­able when using heavily engraved plates.

A further object of the invention is to provide steel die printing inks to be used on web presses which allow to increase printing speed up to 150 m/min. when using a hot air drying device at an air temperature of 100 to 180^oC. Still a further object of the invention is to provide engraved steel die printing inks with improved mechanical resistance to crumpling and flexing and hav­ing outstanding adhesion to highly specified banknote paper carrying gelatin or PVOH-sizing.

SUMMARY OF THE INVENTION

The above mentioned objects and still others are attai­ned by the invention which, in its broadest aspect, is characterized by the fact that the amount of volatile organic solvents in the printing ink is reduced to about 15% by weight or less, referred to the total weight of the ink, typically but not necessarily by the introduc­tion of water.

This has become possible by replacing part of the oleo­resinous compounds in the conventional compositions by resinous matter having a certain degree of hydrophilic properties, due to the presence of polar groups of ionic or nonionic nature. Details will be explained later. This was surprising since one would expect serious dif­ficulties in printing and unacceptable characteristics of the printings obtained on security documents when the resinous phase in the well-balanced overall composition of conventional inks is modified.

DETAILED DESCRIPTION OF THE INVENTION

The printing ink of this invention contemplates composi­tions wherein the solvent concentration, compared to the inks presently available, is reduced. This solvent re­duction may be achieved as such, i.e. in incorporating less solvent than before into a printing ink or in repla­cing part of the amount of organic solvent normally used in known inks by water, or by the combination of these two features.

The applicant has first tried to reduce the solvent con­ tent of printing inks for engraved steel die printing, by replacing the difference in the amount of volatile organic solvents by water or by adding low molecular, well known tensides or soaps, i.e. surface active agents of anionic, nonionic or cationic nature. However, these attempts have been unsuccessful since the required chemi­cal resistances, drying characteristics and non-offsett­ing properties of the printings could never be achieved, and stabilization of water in the ink was impossible.

Now, in trying to facilitate the removal of ink from the wiping cylinders by means of aqueous cleansing composi­tions, which are currently used in the method of en­graved steel die printing, it has surprisingly been found that such oleoresinous components of conventional engraved steel die printing inks which have some weak hydrophilic properties, can in part or even totally be replaced by hydrophilic macromolecular surface active agents or surfactants of different chemical nature. These macromolecular surface active compounds have to be film formers by themselves. They should be compatible with the film forming resins of the ink and should loose most of their hydrophilic properties after the physical and chemical drying of the ink. It has further been found that the film forming reactions allowing to achie­ve this mandatory loss of hydrophilic properties, in or­der to assure the required chemical resistance of the final prints, are oxypolymerisation, interpolymer neutra­lisation and formation of three dimensional interpenet­rating networks. These macromolecular surfactants can be obtained by polymerisation, polyaddition or polyconden­sation reactions. Their synthesis is well known in the art and does not belong to this invention.

The hydrophilic macromolecular surfactants to be used according to this invention are nonionic, anionic or ca­tionic as well as zwitterionic ones. The functional groups attached to these macromolecules are for example carboxylic or sulfonic acid groups, hydroxyl groups, ether groups or primary, secondary, tertiary or quater­nary amino groups. The acid groups may be neutralized with amines, alcanolamines or preferably inorganic bases, or combinations thereof. Primary, secondary and tertiary amino groups may be neutralized with inorganic or or­ganic acids such as sulfonic acids, formic acid, acetic acid, trifluoroacetic acid and others.

Zwitteronic compounds comprise equivalent numbers of acidic and basic groups.

The term "macromolecular surfactant" as used herein shall to be understood as defined e.g. by M.B. Rosen in "Surfactants and Interfacial Phenomena" (John Wiley + Sons 1978) but shall also comprise materials beyond this definition behaving merely as protective colloids. The materials may be used in concentrations up to about 30% by weight of the ink formulation and act at the surface and interface of the numerous components of the ink which are present as solids or liquids.

The macromolecular surfactants which are used according to the invention, have a number average molecular weight in the range from 1000 to 150,000, preferably of from 3000 to 20,000. They may be selected from the hereafter listed classes of surfactants and their mixtures. In particular, the following groups of surfactants are pre­ferred: <ul id="ul0001" list-style="none"><li>A. Nonionic macromolecular surfactants,</li><li>B. Anionic macromolecular surfactants,</li><li>C. Cationic macromolecular surfactants,</li><li>D. Equivalent or non-equivalent mixtures of groups (B) and (C)</li><li>E. Mixtures of macromolecular surfactants of group (A) with such of group (D),</li><li>F. Mixtures of macromolecular surfactants of group (A) with such of group (B) or (C).</li><li>G. Macromolecular surfactants of group A-F with monomolecular surfactants of nonionic, anionic or cationic nature.</li></ul>

The correct selection of the particular macromolecular surfactant composition will depend upon the particular ink composition and may easily be determined by the one skilled in the art by few and simple tests.

Examples of macromolecular surfactants which may be used in the inks of this invention are:

Anionic macromolecular surfactants

These materials are obtained by neutralisation with or­ganic or inorganic bases of the following polymers. <ul id="ul0002" list-style="none"><li>1. Addition reaction products of fumaric acid or maleic anhydride to unsaturated vegetable oils, adducts of phenolic resins and vegetable oils, or polybutadiene type resins (acid number comprised between 10 and 250 mg KOH/g resin), polyamides, polyethers.</li><li>2. Alkyd resins and modified alkyd resins (phenolic, epoxy, urethane, silicone, acrylic or vinylic modi­fied alkyd resins). The acid number is comprised bet­ ween 10 and 150 mg KOH/g resin.</li><li>3. Epoxy resins and modified epoxy resins carrying car­boxylic acid groups. The acid number is comprised bet­ween 30 and 200 mg KOH/g resin.</li><li>4. Saturated polyester resins and modified saturated polyester resins (acid number between 50 and 250 mg KOH/g resin).</li><li>5. Polymers and copolymers containing between 2 and 100% of acrylic acid and/or methacrylic acid and/or maleic acid and/or styrene sulfonic acid (acid number bet­ween 20 and 150 mg KOH/g resin).</li><li>6. Condensation reaction products of rosin and rosin esters with vegetable oils and/or phenolic type re­sins.</li><li>7. Anionic type cellulose ethers.</li></ul>

Nonionic macromolecular surfactants

<ul id="ul0003" list-style="none"><li>1. Block copolymers containing polyether or polyamine sections.</li><li>2. Copolymers based on vinylacetate and other vinyl­monomers of different molecular weight and degree of hydrolysis.</li><li>3. Polyethers and adducts of amines with polyethers.</li><li>4. Polyamines.</li><li>5. Acrylamide type polymers or copolymers.</li><li>6. Polysaccarides and nonionic cellulose derivatives.</li></ul>

Cationic macromolecular surfactants

<ul id="ul0004" list-style="none"><li>1. Salts of epoxy resins or modified epoxy resins carry­ing tertiary or secondary amino groups.</li><li>2. Salts of secondary and tertiary polyamines.</li></ul>

When such macromolecular surfactants are incorporated into the inks of this invention where they replace a portion or the whole of the normally used weakly hydro­philic oleo-resinous compounds, several new effects have been found:

Firstly, relatively high amounts of a water can be in­corporated into the ink in replacement of a portion of the normally used amount of volatile organic solvents, in such proportions that the ink contains up to 30% of water, referred to the total weight of the ink. (All percentages given below refer to that total weight of the printing ink if not otherwise indicated.) It is be­lieved that the macromolecular surfactants act as solu­bilizers or compatibility enhancers for the water to be incorporated. At the same time, and this has already been described, the amount of organic solvent which is typically from 20 to 30%, could be lowered under the mark of 15% and even below 12% and 10% by weight.

The use of a mixture of cationic and anionic macromole­cular surfactants which is accompanied by interpolymer neutralization, is believed to contribute to the complex mechanism of stabilizing water in the ink matrix so as to obtain the necessary rheology for the engraved steel die printing process.

Secondly, it has been found and this was surprising, that the concentration of the aqueous sodium hydroxyde solution used to clean the plastisol or rubber covered wiping cylinder which wipes off the excess ink from the non-image areas of the engraved steel die before print­ ing, can drastically be reduced. For example, when an aqueous NaOH solution of 0.3 to 1% NaOH is typically used, this amount may be reduced to about 0.1% by weight or the solution may even be replaced by deionized water. This advantage of the invention reduces the consumption of hazardous and expensive substances and renders the solution less agressive.

Thirdly, it has been found that in most cases, depending on the nature and the viscosity of the macromolecular hydrophilic surfactants of the invention added to the ink, the amount of solvent in the ink can be reduced without the addition of water. This fact has been highly surprising and can be explained by the particular pig­ment wetting characteristics of the macromolecular film forming surfactants which lead to higher tinctorial strenght and diminish the interactions between the oleo­resinous compounds serving as supplement binder. In some cases, when the rheology and viscosity of the low sol­vent, water-free printing ink should be improved, the high boiling hydrocarbon should partly be replaced by appropriate glycol ethers or other solvents, and/or the content of very high molecular oleoresinous components should slightly be reduced.

Fourthly, it has been proven that the usage of the afore­said macromolecular surfactants allows to improve the bonding of the hardened ink film to highly specified banknote grade papers such as produced by Crane &amp; Co, Portals Ltd., Arjomari, Louisenthal and other specia­lized companies.

Furthermore it was found that the presence of water fa­cilitates the release of the solvent phase after print­ ing favours precipitation of the ink on paper in leaving behind a rather tack free solid. This allows to increase the number of sheets stackable right after printing or respectively to increase machine speed on web presses up to 150 m/min. Furthermore and surprisingly, no interleav­ing is necessary.

Laboratory studies and printing trials on typical prin­ting machines, such as Superintagliocolor 8 or Nota web presses manufactured by König &amp; Bauer, Würzburg, West Germany, for De La Rue Giori, showed clearly that the careful choice of type and quantity of film forming macromolecular surfactants will determine stability of inks on press.

For the printing of paper sheets or the continuous print­ing of paper webs, an ink of the invention contains up to 20% by weight of a solvent phase, 1% to about 8% by weight thereof being water with organic solvents as the remainder, the total amount of organic solvent being not more than 15%, preferably 12% by weight of the ink.

For the printing of paper sheets, another ink of the in­vention contains up to 30% by weight of a solvent phase, about 8% to about 20% by weight thereof being water, with organic solvents as the remainder, the total amount of organic solvent being not more than 12%, preferably less than 10% by weight of the ink.

For the continuous printing of paper webs, an ink of the invention contains up to 35% of a solvent phase, about 8% to about 30% by weight thereof being water, with or­ganic solvents as the remainder, the total amount of or­ganic solvent being not more than 15%, preferably 12%, most preferably 5% by weight of the ink.

The inks of this invention are generally prepared as follows. All parts are by weight:

10 to 80 parts, preferably 10 to 40 parts, more specifi­cally 15 parts of oleoresinous ink binder (I) are mixed with 10 to 60 parts, preferably 20 parts of a film form­ing macromolecular surfactant selected from the aforena­med classes A to G to form an ink base (II) which will be used for grinding of pigments and extenders.

20 to 50 parts of this base (II) are premixed with 50 to 80 parts of pigments and/or extenders on a butterfly mixer as e.g. manufactured by Bühler in Switzerland or Molteni in Italy.

This premixed paste is then transferred to a grinding equipment such as three roll-mills e.g. 1300 SDVE as manufactured by Bühler of Switzerland or any other grinding equipment such as continuously working ball or bead mills such as cobal mill MS50 manufactured by Fryma in Rheinfelden, Switzerland. The grinding process is stopped as soon as a fineness of less than 10 microns is obtained. The pigment paste is then transferred to a heavy duty mixer as e.g. a Vollrath VDDX 80, manufactu­red by Vollrath in West-Germany for the optional intro­duction of deionized water and other ink additives such as wax compounds, drying catalysts, antioxydants and other ingredients known to be useful in printing ink fomulations.

The manufacturing process finishes with a 30 to 40 minu­tes mixing operation under vacuum of 0.01 to 0.1 bar in order to take out any dispersed air. At this stage the paste ink is presented to the laboratory of quality as­surance for final check of colour characteristics, rheo­logy and printing performance. The necessary equipment is the same as for conventional printing inks and does not need to be described here.

Generally the viscosity of this new type of intaglio inks for the engraved steel die printing process is com­prised within 1 to 15, more specifically within 3 to 8 Pa.s at 40^oC and a shear rate of 1000 sec⁻¹.

The water containing intaglio inks manufactured in the now described manner are products being stable in time at temperatures within -30 to + 50^oC for more than 1 year.

As oleoresinous compounds (I) the following types of re­sins can be used: medium to long oil content alkyd re­sins, vinyl-acrylic, siloxane, phenolic resin or ure­thane modified alkyd resins, addition products of pheno­lic resin or rosin esters to vegetable oils or polybuta­dien derivatives, mineral oil soluble copolymers, epoxi­de resins, epoxide esters of fatty esters or any other film forming conventional binder useful for printing ink formulation.

The remaining components of the engraved steel die print­ing inks of the invention are substantially the same as in the inks known heretobefore, with the exception of the reduced amount of oleoresinous components and of the presence of a polar phase as part of the oleoresinous component, allowing stabilisation of water within the ink system without altering chemical and mechanical re­ sistances of the final print. The level of these resis­tances has been strictly recommended by the fifth Inter­national Conference on currency and counterfeiting by the International Criminal Police Organization (INTERPOL).

The invention now permits to fit in even with the most stringent legislation in that the content of volatile organic solvents of the printing ink could be decreased under the mark of 12%, even 10%, by weight.

The following Examples are only given for the purpose of a better understanding of this invention. They will not limit the scope thereof. All parts are by weight.

Example I Sheet fed intaglio ink

Part I

Preparation of the macromolecular surfactant (rosin modi­fied phenolic type):

60 parts of rosin modified phenolic resin are first re­acted with 25 parts of raw tung oil at 220^oC for two hours. The product is then dissolved in 15 parts of a mineral oil (boiling range 170 - 260^oC). The acid number is situated between 75 and 90 mg KOH/g resin. The number average molecular weight, determined by GPC analysis, is 2000 g/mol. Finally, the product is neutralized with an aqueous solution of 25% potassium hydroxyde to a pH of 8. The final acid value is below 10 mg KOH/g resin.

Part II

A water containing, non-interleaving intaglio ink is manufactured according to the following formula: <tables id="tabl0002" num="0002"><table frame="all"><tgroup cols="2" colsep="1" rowsep="0"><colspec colnum="1" colname="col1" colwidth="78.75mm" /><colspec colnum="2" colname="col2" colwidth="78.75mm" /><tbody valign="top"><row><entry namest="col1" nameend="col1" align="right">15</entry><entry namest="col2" nameend="col2" align="left">parts of macromolecular surfactant as described in part I.</entry></row><row><entry namest="col1" nameend="col1" align="right">8</entry><entry namest="col2" nameend="col2" align="left">parts of alkylphenolic tung oil adduct diluted in a high boiling point oil (Magie 500) to a solids content of 80%.</entry></row><row><entry namest="col1" nameend="col1" align="right">10</entry><entry namest="col2" nameend="col2" align="left">parts of long oil alkyd resin diluted in a high boiling print mineral oil (Magie 500) to a solids content of 80%.</entry></row><row><entry namest="col1" nameend="col1" align="right">2</entry><entry namest="col2" nameend="col2" align="left">parts of the sodium salt of sulfonated castor oil in water (solids content 60%).</entry></row><row><entry namest="col1" nameend="col1" align="right">2</entry><entry namest="col2" nameend="col2" align="left">parts of micronized polyethylene wax.</entry></row><row><entry namest="col1" nameend="col1" align="right">3</entry><entry namest="col2" nameend="col2" align="left">parts of a high boiling point mineral oil (Magie 500).</entry></row><row><entry namest="col1" nameend="col1" align="right">8</entry><entry namest="col2" nameend="col2" align="left">parts of pigment blue 15 (IRGALITHE blue BL, Ciba-Geigy).</entry></row><row><entry namest="col1" nameend="col1" align="right">35</entry><entry namest="col2" nameend="col2" align="left">parts of calcium carbonate.</entry></row><row><entry namest="col1" nameend="col1" align="right">2</entry><entry namest="col2" nameend="col2" align="left">parts of a multi metallic dryer (octoacte salts of cobalt, manganese and zirconium diluted in a high boiling point mineral oil to a solids content of 85%).</entry></row><row><entry namest="col1" nameend="col1" align="right"><u style="single">15</u></entry><entry namest="col2" nameend="col2" align="left">parts of deionized water thickened with a cellulose ether.</entry></row><row rowsep="1"><entry namest="col1" nameend="col1" align="right">100</entry><entry namest="col2" nameend="col2" /></row></tbody></tgroup></table></tables>

All the components except dryer and water are mixed to­gether for 20 minutes at room temperature on a Molteni mixer, then ground on a three roller-mill in order to achieve a fineness below 10 µm. Then the dryer and the water are added, mixed for 15 mn, and deaerated under vacuum on a Molteni mixer. The viscosity of the ink is 10 Pa.s at 40^oC and the volatile organic content does not exceed 8%. The ink shows a very easy wipability and detergability, excellent non-offsetting properties, and dries perfectly over a period of 24 hours. The prints show excellent chemical and mechanical resistances.

Example II Sheet fed intaglio ink

Part I

Preparation of the macromolecular surfactant - acrylic modified alkyd type:

An alkyd resin containing pentaerythritol, ethylene gly­col and glycerol monoallyl ether as polyols, isophtalic acid and maleic anhydride as polyacids, and tall oil fatty acid as fatty acid is prepared by polycondensation at 220^oC to an acid number of 10 mg KOH/g. The product is then diluted to a solids content of 60% with methyl ethyl ketone. Acrylic acid, butyl methacrylate, and ben­zoyl peroxide are then added, and the mixture is heated to 80^oC - 120^oC for three hours. Methyl ethyl ketone is removed, and the product is diluted with a high boiling point mineral oil (Magie 500) to a solids content of 80%. The final acid value is between 40 and 50 mg KOH/g resin, and the number average molecular weight, determi­ned by GPC analysis, is about 3500 g/mol. Finally the product is neutralized with a 10% lithium hydroxyde aqueous solution to a pH of 7.5. The final acid value is below 15 mg KOH/g.

Part II

A water containing, non interleaving intaglio ink is manufactured according to the following formula: <tables id="tabl0003" num="0003"><img file="EP0340163A2_D0002.tif" /></tables>

All the components except dryer and water are mixed to­gether for 20 minutes at room temperature on a Molteni mixer, then ground on a three roller mill in order to achieve a fineness below 10 µm. Then the dryer and the water are added, mixed in for 15 mn and deaerated under vacuum on Molteni mixer. The viscosity of the ink is about 8 Pa.s at 40^oC and the product shows excellent machine performance and fulfills all requirements for security document printing.

Example III Heat set intaglio ink

Part I

Preparation of the macromolecular surfactant:

A medium length alkyd resin carrying carboxylic groups is synthesized by polycondensation at 220^oC of penta­erythritol, phthalic anhydride and linseed oil fatty acids to an acid number below 10 mg KOH/g resin and further addition of phthalic anhydride at 150^oC which is allowed to react for one hour to an acid number of 60 mg KOH/g resin. The product is then diluted in a high boiling point mineral oil (Magie 500) to a solids con­tent of 80%. The number average molecular weight, deter­mined by GPC, is about 3000 g/mol. The product is then neutralized with a 20% aqueous solution of lithium hydroxyde to a final pH of 8.

Part II

A heat-set, water-containing intaglio ink is manufactu­red according to the following formula: <tables id="tabl0004" num="0004"><table frame="all"><tgroup cols="2" colsep="1" rowsep="0"><colspec colnum="1" colname="col1" colwidth="78.75mm" /><colspec colnum="2" colname="col2" colwidth="78.75mm" /><tbody valign="top"><row><entry namest="col1" nameend="col1" align="char" char=".">20</entry><entry namest="col2" nameend="col2" align="left">parts macromolecular surfactant as described in Part I,</entry></row><row><entry namest="col1" nameend="col1" align="char" char=".">11</entry><entry namest="col2" nameend="col2" align="left">parts high melting point, rosin modified phenolic resin dissolved in a long oil alkyd resin and high boiling point mineral oil (Magie 500) to a solids content of 60%,</entry></row><row><entry namest="col1" nameend="col1" align="char" char=".">2</entry><entry namest="col2" nameend="col2" align="left">parts high boiling point mineral oil (Magie 500),</entry></row><row><entry namest="col1" nameend="col1" align="char" char=".">8</entry><entry namest="col2" nameend="col2" align="left">parts pigment blue 15 (Irgalithe blue BL-Ciba-Geigy),</entry></row><row><entry namest="col1" nameend="col1" align="char" char=".">32</entry><entry namest="col2" nameend="col2" align="left">parts calcium carbonate,</entry></row><row><entry namest="col1" nameend="col1" align="char" char=".">3</entry><entry namest="col2" nameend="col2" align="left">parts sodium salt of sulfonated castor oil in water (solids content 60%),</entry></row><row><entry namest="col1" nameend="col1" align="char" char=".">2</entry><entry namest="col2" nameend="col2" align="left">parts micronized polyethlene wax,</entry></row><row><entry namest="col1" nameend="col1" align="char" char=".">1.5</entry><entry namest="col2" nameend="col2" align="left">parts multi-metallic dryer (octoacte salts of cobalt, manganese and zirconium dissolved in a high boiling point mineral oil to a solids content of 85%), and</entry></row><row><entry namest="col1" nameend="col1" align="char" char="."><u style="single">20.5</u></entry><entry namest="col2" nameend="col2" align="left">parts deionized water.</entry></row><row rowsep="1"><entry namest="col1" nameend="col1" align="char" char=".">100</entry><entry namest="col2" nameend="col2" /></row></tbody></tgroup></table></tables> The manufacturing process is the same as given in Example I.

The new inks of the invention are used in the same man­ner as the inks known before. They are valuable composi­tions for the printing of security documents, such as banknotes, checks, traveller checks, credit cards, stamps, shares, passports, airline tickets, lables and similar documents for which measures against counter­feiting and forgery are necessary or indicated.

The preceding description clearly shows the surprising compositions of this invention. It is evident that the practical realization of the invention in the context of the claimed matter may be varied or modified according to the knowledge of the man skilled in the art without departing from the principles and the scope of this in­vention. Particularly in the field of printing, numerous modifications and improvements are possible in the for­mulation of printing inks. However, such modifications and improvements are comprised in the scope of protec­tion of this invention.