This invention is concerned with ink containing reactive diluent which comprises oxidatively curable ester containing addition polymerizable ethylenic unsaturation and drying oil residue, methods of printing using the ink and substrates marked with cured ink.

Lithography is usually reserved for high quality printing, such as advertising, books, publications, and packaging. Lithographic inks are divided basically into two types; so-called heat-set and quick-set.

Lithographic ink users consider that suitable resins and components for heat-set inks and quick-set inks should have the following characteristics:

• 1) Magie Oil solvent (aliphatic hydrocarbon) solubility
• 2) Fast-drying without excessive energy input
• 3) Compatability with resinous ink vehicles
• 4) Low odor
• 5) Pigment dispersing and wetting capability
• 6) Good transfer properties
• 7) Stability on the press (antiskinning and viscosity stability)
• 8) Water immiscibility
• 9) Gloss
• 10) Low tendency to attack rubber printing rolls and blankets
• 11) Resistance to rubbing

Commercial lithographic inks are high viscosity paste inks, mainly comprising colored pigment, binder resin, or resinous vehicle and solvent, usually high boiling aliphatic petroleum cuts known as "ink oils." Solvent content is from about 30% to 50% by weight. Minor additives include natural and synthetic waxes, metal salt driers, antioxidants, antiskinning agents, "sweetening" stronger solvents such as tridecyl alcohol (U.S. patent No. 3,257,344), and gelling or bodying agents such as aluminum ortho esters (U.S. patent No. 3,531,302). The resins are usually high melting (_>60°C) so as to yield hard, non-offsetting, block-resistant and rub-resistant films. Suitable resins are hydrocarbon polymers, rosin derivatives, alkyds, acrylics, styrene-acrylics, and other conventional binders.

"Quick-set" lithographic inks frequently use the higher boiling of the ink oils, such as Magie Oil 535 as solvent and dry at ambient temperature by a combination of evaporation, wicking into paper, and precipitation via design for marginal resin compatibility "Heat-set" types use lower boiling solvent such as Magie Oil 470 to achieve faster setting, and are dried at very high speeds in ovens, usually gas fired. These "oils" consist essentially of aliphatic hydrocarbons and are described below.

In the heat-set area especially, the printing industry is under increasing regulatory agency pressure to drastically reduce polluting solvent emission. ink solvent emission is particularly noxious because the high boiling point ink oil solvents required for long term viscosity stability on the press yield dense smoke plumes from the stacks.

U.S. Patents 3,766,110 and 3,776,867 disclose solvent-free printing inks based on acid catalysed urea or melamine formaldehyde resins with hydroxyl functionality. They are certainly free of solvent emission but do emit noxious and toxic formaldehyde cure. Moreover, it is well know that such systems have limited shelf life, especially with the strong acid catalysts required for acceptably low cure temperatures.

U.S. Patent No, 3,284,385 discloses the preparation of and anionic polymerization of methacryloxyethyl linoleate, acryloxyethyl linoleate, and drying oil fatty acid analogs. Also, U.S. Patent No, 2,160,532 discloses the preparation of monomeric mixed esters of polyhydric alcohols such as diols, glycols, etc., with methacrylic acid and drying oil acids. Specifically disclosed are soybean oil diglyceride monomethacrylate, soybean oil monoglyceride dimethacrylate, glycol laurate methacrylate (lauryl alcohol is a saturated alcohol), and related materials. These are used in coatings with peroxide initiators or metal salt driers or with other resins. U.S. Patent No. 2,593,444 discloses esters of acrylic or methacrylic acid and alcohols derived from drying oils. The use of heat settable inks containing drying oil functionality is also known. See for example Chem. Abstr. 82, 141786R.

We have now found certain oxidatively curable liquid reactive diluents having low viscosity and low volatility which may be used to prepare high solids lithographic inks. The inks may have exceptional storage stability and, by avoiding the use of volatile solvent, reduce atmospheric pollution by such solvents and conserve them, saving valuable raw materials. By "high solids" is meant the materials which remain in the cured ink; thus, the reactive diluent is calculated as part of the "solids".

According to the invention there is provided a lithographic ink containing colorant, binder resin and reactive diluent, wherein the diluent comprises oxidatively curable ester produced by the reaction of:

• (a) drying oil fatty acid, or transesterifiable ester thereof, with
• (b) hydroxyl-containing reaction product of at least one polyol with addition polymerizable carboxylic acid, or transesterifiable ester thereof; or by the reaction of:
• (c) addition polymerizable carboxylic acid, or transesterifiable ester thereof, with
• (d) hydroxyl-containing reaction product of at least one polyol with drying oil fatty acid, or transesterifiable ester thereof; provided that when component (a) comprises drying oil fatty acid, the other component may be
• (e) other hydroxy-containing addition polymerizable compound.

Preferably, the reactive diluent comprises one or more acryloxy alkyl or methacryloxy alkyl drying oil fatty acid esters.

Preferred ink compositions of the invention contain liquid reactive diluents preferably of the formula:

where -R¹ is -H or -CH3 R² is an aliphatic radical, preferably linear hydrocarbyl, having 11-23 carbon atoms and containing at least one olefinic double bond, or mixtures thereof, -R², being free of terminal double bonds, and -X- is either -OR³0- in which R is an aliphatic or cycloaliphatic hydrocarbon residue containing from 2 to 10 carbon atoms, or -O(CH₂CHR⁴O)_n- where R⁴ is -H or -CE₃ and n is an integer from 2-10, or mixtures thereof.

Preferably, X is -OR³0- in which R³ is -CH₂CH₂-or

and -R is linear hydrocarbyl, is at least in part polyunsaturated, more preferably predominantly polyunsaturated, and is a mixture of moieties derived from one or more drying oils.

While those compounds of the given formula are preferred, as will be explained hereinafter, not only derivatives of acrylic or methacrylic acid are useful, but also compounds based on α,β -olefinically unsaturated hydroxyalkyl monocarboxylic or polycarboxylic acids, and hydroxyalkyl vinyl sulfides and ethers, and the like, are also included. Thus, in its broader aspects, the reactive diluent may be considered to be the drying oil fatty acid ester of any addition polymerizable olefinically unsaturated hydroxyl-containing compound. Thus, one way of making the reactive diluents is by esterification of an addition polymerizable olefinically unsaturated hydroxy-containing compound with drying oil fatty acids. Suitable hydroxy-containing compounds include the following materials, which can be used to prepare reactive diluents of the formula given above, directed to the acrylic acid or methacrylic acid derivatives, as well as those which are less preferred but are also useful: 2-hydroxyethyl acrylate, methyl α(hydroxymethyl)-acrylate, ethyl α(hydroxymethyl)-acrylate, butyl (2-hydroxyethyl)-acrylate, 2-hydroxypropyl acrylate or methacrylate, 3-hydroxypropyl acrylate or methacrylate, methyl (2-hydroxypropyl)-acrylate., ethyl -(3-hydroxypropyl)-acrylate, 4-hydroxybutyl acrylate, 5-hydroxyamyl acrylate, 6-hydroxyhexyl acrylate, 7-hydroxyheptyl acrylate, 8-hydroxyoctyl acrylate, 9-hydroxynonyl acrylate, 10-hydroxydecyl acrylate, 2-hydroxyethyl methacrylate, 6-hydroxyhexyl methacrylate, 8-hydroxyoctyl methacrylate, 10-hydroxydecyl methacrylate, 3-hydroxyprcpyl crotonate, 5-hydroxyamyl crotonate, S-hydroxyhexyl crotonate, 7-hydroxypheptyl crotonate, 10-hydroxydecyl crotonate, di(2-hydroxyethyl)maleate, di(4-hydroxybutyl)-maleate, di(6-hydroxyhexyl)maleate, di(9-hydroxynonyl)maleate, di(10-hydroxydecyl)maleate, di(2-hydroxyethyl)fumarate, di(4-hydroxybutyl)fumarate, di(6-hydroxyhexyl)fumarate, di(10-hydroxydecyl)fumarate, and the like Additionally, other substituents may be incorporated into the alkyl chain, including secondary hydroxy groups, halide radicals, nitrile radicals, and the like, such as 2,3-dihydroxypropel acrylate, 3,5-dihydroxyamyl crotonate, 6,10-dihydroxycecyl methacrylate, di-2,6-dihydroxyhexyl maleate, di-2-cnloco 7-hydroxyheptyl fumarate and the like In all cases, the hydroxyl of each hydroxyalkyl is at least two carbon atoms removed from the carbon atom of the adjacent -COO- radical in the ester.

A broader definition of the diluents useful in the invention is that they are esters of drying oil fatty acids with hydroxyalkyl esters of α,β -olefinically unsaturated, addition polymerizable, monocarboxylic or polycarboxylic acids. In addition, olefinically unsaturated hydroxyalkyl vinyl sulfides and vinyl ethers may be used to form esters with the drying oil fatty acids to give useful reactive diluents.

Examples of the vinyl sulfides and vinyl ethers include:

• f-Bydroxyetheyl vinyl sulfide
• p-Hydroxyethyl vinyl ether
• β-Hydroxypropyl vinyl sulfide
• 5-Hydroxypentyl vinyl ether
• 6-Hydroxyhexyl vinyl ether
• 8-Hydroxyoctyl vinyl ether
• 10-Hydroxydecyl vinyl ether
• Diethyleneglycol monovinyl ether

Kirk-Othmer, "Encyclopedia of Chemical Technology", Volume 8, pages 395-398, Interscience, New York (1952), discusses the mechanism of oxidative drying. It is indicated that peroxides are formed, that conjugation of the double bonds in the oils occurs at least to some extent, followed by crosslinking of the oils in the film. It is believed that such peroxides cause addition polymerization of the α,β -ethylenic unsaturation in the reactive diluents of the invention. Thus, while it is important that some polyunsaturated drying oil acids be present in order for peroxides to be formed, once the peroxides are present to act as free radical initiators for the addition polymerization, the adducts of, e.g., hydroxyethyl methacrylate with any of oleic, palmitic, or stearic acids are believed to undergo addition polymerization. This theory is confirmed by I. R spectroscopic analysis, which shows no residual methacrylate unsaturation, for instance, in the fully cured ink. Of course, it is possible to add a free conventional radical initiator, but such material is not needed.

The reactive diluents of the present invention are highly compatible with common ink resins and may be used to replace some or all of the volatile solvent. They are virtually non-volatile for the times and at the temperatures commonly used in heat setting and they cure in air with transition metal driers or siccatives, such as cobalt and manganese salts, to become a part of the film forming mass. Inks of the invention containing metal drier salts and low levels of volatile inhibitors such as oximes, may have exceptional shelf stability. The inks may also provide excellent pigment wetting and high ink gloss, and low tendency to swell Neoprene and Buna N press blankets and rollers used extensively in the industry. The reactive diluent preferably comprises frcm 5% to 50% by weight of the comblned welghts of the reaotive diluent and binder resin.

While the reactive is preferably the sole diluent in the inks of this invention, it can be mixed with conventional volatile solvents. Sucn cnnventional solvents have a Kauri-butanol (KB) value of between 18 and 31, preferably between 21 and 28. Typical products have a minimum of about 70% paraffins, i.e., consisting essentially of saturated aliphatic or cycloaliphatic hydrocarbons, with no more than abour 25% romaies, on a weight basis. They may contain small percentages of aliphatic olefins, such as less thar 10% preferably less than about 5%. The averarge molecular waight is preferably between 160 and 270. Usually they have an initial boiling point of between about 204°C (400°P) and about 315°C (600°F) with a final boiling point of between about 246°C (475°F) and 371°C (700°F). The preferred initial boiling point is between about 204°C (400°F) and 26₀°C (500⁰F) with a final boiling point of between 246°C (475°F) and 315°C (600°F). The aniline point is between about 65°C (150°F) and 104°C (220°F). Suitable products are available from Magie Bros. Oil Company, 9101 Fullerton Avenue, Franklin Park, Illinois 60131, United States of America. Suitable products are sold as Magie Oil 400, 405, 415, 440, Deo 440, 470, 4600, 500, Deo 520, 535, 5300, 590, 625, and Deo 620. Other boiling ranges are usable provided the KB value is as specified. The kauri-butanol value is the number of milliliters of the hydrocarbon or other liquid required to cause cloudiness when added to 20g of a solution in which there is lOOg of kauri gum and 500g of butyl alcohol. This is basically ASTM method D-1133, Volume 20.

Any of the conventional ink colorants may be used in the inks of this invention, for example carbon black, phthalocyanine blue, titanium dioxide, lithol rubine reds, ultramarine blue and hansa yellow. A suitable colorant or pigment:binder resin plus reactive diluent ratio is from 0.01:1 to 2:1, on a weight basis.

Typically, lithographic inks are soft to medium to heavy pastes, having a viscosity of from 5,000 cps to 500,000 cps at 25°C.

Preferably the ink of the invention is free of inert of volatile solvent.

The solid binder vehicle may contain conventional resins. Fossil resins such as gilsonite, rosin esters of glycerol or pentaerythritol, limed rosin, maleic modified rosin, alkyds, phenolic resins, hydrocarbon resins and acrylic polymers are useful. Among the conventional ink resins are rosin-derived resins such as the phthalate esters of hydroabietyl alcohol, wood rosin, polymerized rosin, /maleic-modified rosin, and phenolic modified rosin. Also useful are aromatic and aliphatic hydrocarbon resins and copolymers such as vinyl toluene and -methyl stvrene, These are available from the Resins Division nf Heroules Inc., Wilmington, Del. 19859, United States of America, Acrylics such as those disclosed in Belgian Patent No. 863,624 are useful. These are low molecular weight (Mw 1,000-15,000) acrylic polymers of 1-40% by weight isobornyl methacrylate and one or more of isobutyl methacrylate, tert-butylaminoethyl acrylate, methacrylic acid, dimethylaminoethyl methacrylate, dimethylaminoethyl acrylate, acrylic acid, maleic anhydride, itaconic acid, oxazolidinyl ethyl methacrylate and styrene. Other suitable comonomers include dicyclopentenyl methacrylate and acrylate, dicyclopentenylethoxy methacrylate and acrylate, butyl methacrylate, dicyclopentenylneopentoxy methacrylate and acrylate, isobornyl acrylate and other vinyl aromatics such as α-chlorostyrene,α-methyl styrene, t-butyl styrene and vinyl toluene. Typically, a small amount of carboxylic acid monomer such as acrylic acid and/or methacrylic acid is included. Typieal polymers are isobutyl methacrylate/isobornyl methacrylate/methacrylic acid in the weight ratio 66/29/2; isobutyl methacrylate/isobornyl methacrylate/t-butyl amiroethyl methacrylate/methacrylic acid in the weight ratio 68/28/3/1; isobutyl methacrylate/vinyl toluene/methacrylic acid in the weight ratio 29/69/2; and s-butyl methacrylate/ methacrylic acid in the weight ratio 98/2.

The reactive diluents in this invention may be prepared by any of the methods taught by U.S. Patent No. 3,284,385 or U.S. Patent No. 2,160,532. As an alternative to esterifying the hydroxyl compound, e.c., hydroxyethyl methacrylate, with the fatty acid, the fatty acid may first be converted to the monoester of a glycol, followed by esterification with, e.g., methacrylic acid or transesterification with methyl methacrylate.

This alternative method of preparing the reactive diluent entails a two-stage esterification in which the fatty acid is first reacted with a large excess of glycol and the resultant product then esterified with , e.g., acrylic or methacrylic acid. An excess of glycol is required in order to prevent the formation of the bis (fatty acid) ester, R²C0₂R³0₂CR³. The reverse sequence, esterification of the polymerizable acid first, is preferred, since such products are commercially available. Transesterifications of lower alkyl esters of the acids may be employed as well at each stage of either process. The alternative procedure is illustrated by the equations:

It thus is to be understood that when reference is made, e.g., to an ester of the drying oil acids with an unsaturated hydroxyl-containing acid, esters made by this alternative method are included. Another way of describing the preferred reactive diluents of the invention is to define them as the mixed esters of (1) mixed natural drying oil fatty acids and (2) an α,β ethylenically unsaturated acid with a polyol.

Typical examples of unsaturated acids useful in the invention, particularly as naturally occuring mixtures, are:

• 9,12 linoleic acid,

  Linolenic acid,

  Arachidonic acid,

  Licanic acid,

  Parinaric acid,

  Eleosteric acid,

  Palmitoleic acid,

  Oleic acid,

  Petroselinic acid,

  Vaccenic acid,

  Cetoleic acid,

The polyunsaturated drying oil acid moieties are preferred. These acids are obtained by the well known catalytic hydrolysis of the corresponding natural or synthetic fatty esters. Of course, mixtures of the acids are commonly used, because there is no need to separate the acids obtained from a given drying oil. Mixtures of acids from more than one drying oil are also useful.

It may be noted that in these mono-olefinic and poly-olefinic R²COOH- groups, there is no terminal CH2=C < structure. Instead, the terminal group is a -CH₃ group. Moreover, the first double bond in the structure is removed from the oxygen from of its esters by at least 4 carbon atoms and by as many as 14 carbon atoms, and therefore are nor activated by the ester structure. Furthermore, the first double bonds are removed by at least 1 carbon atom from the terminal -CH₃ group which is not an activating group. Finally there may be 1 to 4 or more -CH=CH - groups in the fatty acid residue.

Table 1 gives the percentage composition of the fatty acids in a number of drying oils, which on hydrolysis produce relative proportions of the corresponding acids.

It will be noted in Table 1 that all of the oils have measurable amounts of compounds having one or mere than one double bond in the fatty acid, and therefore, the derived acids have a substantial amount of suitable mcnc- and poly-unsaturation suitable for the purposes of this invention.

Among the drying oils from which the drying oil fatty acid is derived are linseed, tung, tall, safflower, perilla, soya, dehydrated castor, maleinized or fumarized linseed, oiticica, palm, peanut, corn, walnut, menhaden, dehydrated castor, and cottonseed oils, and similar oils, as well as acids not derived from drying oils and of a synthetic origin, with a carbon chain preferably of about 23 carbon atcms or less and having unsaturation therein which can be caused to air cure in a manner analogous to linseed oil. Preferred sources cf the drying oil acids are tung, linseed, safflower, soybean and dehydrated castor oils.

At times it is beneficial to include a polyolefinieally unsaturated addition polymerizable crosslinker in the ink along with the reactive diluent. Suitable polyunsaturated copolymerizable cross-linking compounds include; divinylbenzene, divinylpyridine, divinyltoluenes, divinylnaphthalenes, diallyl phthalate, ethylene glycol diacrylate, ethylene glycol dimethacrylate, divinylxylene, divinylethylbenzene, divinylsulfone, divinylketone, divinylsulfide, allyl acrylate, diallyl maleate, diallyl fumarate, diallyl succinate, diallyl carbonate, diallyl malonate, diallyl oxalate, diallyl adipate, diallyl sebacate, divinyl sebacate, diallyl tartrate, diallyl silicate, triallyl tricarballylate, triallyl aconitate, triallyl citrate, triallyl phosphate, N,N'-methylenediacrylamide, N,N'-methylene dimethyacrylamide, a 1,3-butylene glycol di(meth)acrylate, a trimethylol propane tri(meth)-acrylate, N,N'-ethylenediacrylamide, trivinylbenzene, trivinylnaphthalene, polyvinylanthracenes and the polyallyl and polyvinyl ethers of glycol, alycerol, pentaerythritol, resorcinol and the monothio or dithio derivatives of glycols. The proportion of crosslinker is frcm 0% to 50%, preferably 0.05% to 30% of the weight or the reactive diluent.

In making the hydroxyl-containing addition polymerizable compound or the drying oil fatty acid monoester of a diol, various diols are useful. These include ethylene glycol, diethylene glycol, triethylene glycol, tetraethylene glycol, propylene glycol, dipropylene glycol, 1,3-butanediol, 1,4-butanediol, 2,3-butanediol, 2-butene-l,4-diol, 1,5-pentanediol (pentanediols), 1,6-hexanediol (hexanediols), heptanediols, 1,8-octanediol (octanediols), nonanediols, decanediols, 2,2,4-trimethyl-1,3-pentanediol, 2,2-diethyl-l,3-butanediol, 2-ethyl-l,4-butanediol, 3,3-diethyl-l,5-pentanediol, 2,2-dimethyl-1,3-propanediol, 2,2-dimethyl-l,3-hexanediol, 2-ethyl-1,3-hexanediol, 2,2-diethyl-l,3-propanediol, 3-methyl-1,4-pentanediol, 1,2-cyclohexanediol, 1,4-cyclohexanediol () cyclohexanedineethanol bisphenol A, hyde malet lspenol A, etc. or mixtures thereof.

Any of the conventional driers or siccatives, such as the linoleates, naphthenates, and rasinatas of cobalt, zirconium, manganese, lead, ceriam chromium, iron, nickel, uranium, and zinc are suitable for curing the inks of the invention. Inorganic acid salts can also be used.

The amount of drier if used, based on the weight of the reactive diluent, can be as low as 0.001% to as high as 3% or more. Good results are often obtained with combinations of driers, such as zinc naphthenate and cobalt naphthenate in quite small amounts, for example, from .01% to 0.5% of the zinc naphthenate together with 0.01% to 0.1% cobalt naphthenate. Co⁺⁺ is also useful, alone or with compounds providing Mn⁺⁺ Zn⁺⁺Zr⁺⁺ , or pb⁺⁺ .

The drier may be added to the link composition prior to storage. If a volatile stabilizer is included in the composition to inhibit or prevent the oxidizing action of the drier, the composition is preferably placed in closed storage containers to prevent volatilization of the stabilizer. The stabilizer may be used in a proportion of 0 to 2% by weight based on the weight of the binder and reactive diluent. The stabilizer is generally a volatile ketone-oxime or aldehyde-oxime. Specific examples are methyl ethyl ketone-oxime, methyl butyl ketone-oxime, 5-methyl-3-heptancne-oxime, cyclohexanone-oxime, and butyraldehyde-oxime. Addition of such inhibitors is not essential to long stability and pot life of the inks. In some cases, antioxidants such as hydroquinone can be included without seriously inhibiting the cure of the ink

One embodiment of the invention provides a method cf printing by lithography which comprises applying ink of the invention to a printing device, transferring at least some of the ink from the device to a substrate and curing the ink or allowing it to cure.

The ink of this invention may be applied to a substrate and after absorption by the substrate, such as paper, and evaporation of volatile solvent, if used, the ink is cured by oxidative drying.

Other substrates than paper are useful for making printed articles. Such materials include plastics, such as polyolefins, metals and other cellulosic materials.

The invention also provides a printed article bearing the ink of the invention in cured form.

Another method of caring the take of the invention is by the ase of wave energy such as ultraviolet light. In that method, the ink includes a small amount of a conventional photoinitiator such as Michler's ketane, a benzoin ether, or benzophenone.

The monomers included herein are of commercial purity; that is, they may contain small amounts of other materials. For example, hydroxymethyl methacrylate (ethylene glycol mono- methacrylate) normally contains small amounts of the dimethacrylate. This may even be an advantage, since, as noted above, small amounts of polyunsaturated orosslinkers are often useful.

Typical analyses of hydroxyethyl methacrylate (HEMA) and hydroxypropyl methacrylate (HPMA) show that normally the products contain small amounts of methacrylic acid, hydroxyalkoxyalkyl methacrylate, and dimethacrylates (ethylene dimethacrylate in HEMA and propylene dimethacrylate in HPMA). Typical analyses (not specifications) are:

HPMA is a mixture in which the hydroxyalkyl methacrylate is principally 2-hydroxypropyl methacrylate, with some 1-methyl-2-hydroxyethyl methacrylate. While it can be done, it is not necessary to further purify the raw materials used to make the reactive diluents. The polymerization inhibitors usually present need not be removed.

Some preferred embodiments of the invention will now be more particularly described in and by the following examples, in which all and percentages are by weight unless eitherweise stated

Example A

Preparation of Methacrvloxyethyl Linseed Oil Fatty Acid Esters

A 5000 ml four-necked flask, equipped with a thermometer, air ebullator, mechanical stirrer, Dean-Stark trap and condenser, was charged with 1366.9 g linseed oil fatty acids (Procter and Gamble L-31D, eq. wt: 267 g, 7.0 equiv.), 960.0 g hydroxyethyl methacrylate (7.0 equiv., inhibited with about 1,000 ppm of the methyl ester of hydroquinone), 6.72 g methane-sulfonic acid (0.07 equiv.) 0.47 g phenothiazine, and 450 g heptane. The mixture was heated to reflux and water generated in the reaction was removed by azeotropic distillation. Upon completion of the reaction (4-5 hours), the flask was cooled to 50°C and the catalyst was neutralized with 11.6 g of a 50% sodium hydroxide solution. Removal of the heptane in vacuo and filtration of the residue through Celite 545 afforded 2525 g of dark red product (93.3%), Brookfield Viscosity: 15 cps. at 25°C.

Example 1 - Preparation and Use of a Rich Solids Heat Set Lithographic Ink

A base ink vehicle solution is prepared, for convenience, by dissolving 60 parts of a hard synthetic rosin ester resin (Pentalyn® G) in a mixture of 20 parts of Magie Oil 470 ink solvent and 20 parts of the 2-hydroxyethyl methacrylate esters of linseed oil fatty acids, as prepared in Example A as the non-volatile reactive diluent.

A blue ink is prepared by pigmenting and formulating the above vehicle solution with aid of a Hoover Automatic Muller (Hoover Color Corporation) using 150 pounds pressure for 300 cycles. Approximately 7 parts of the following recipe are charged:

The solids content of the ink is 83 percent by weight. If the ink is made in conventional fashion, i.e., by replacing the linseed oil fatty ester with volatile ink oil, the solids content is only 57% by weight.

Proofs of the high solids ink are made on web paper stock using a "Little Joe" Offset Color Swatching Press, Model S-77. The ink exhibits excellent wetting and transfer. The proofs are dried in a laboratory heat set oven ("Sinvatrol" Tester, Sinclair & Valentine Co.), at speeds up to 50 feet per minute at an air temperature of 149°C (300°F). The proofs dry to a non-offsetting condition, and cure to yield films having excellent rub resistance. They also exhibit excellent gloss and tint strength, indicative of good pigment wetting and hold-cut on the paper. Moreover, the wet ink exhibits excellent storage stability.

Pentalyn® G (Hercules Incorporated), is a dibasic acid modified rosin ester having an estimated softening point of 126°C by ASTM ring-and-ball method E28-67; an acid number of 14 , and a specific gravity of 1.10 at 25°C.

Magie Oil 470 is a heat set ink hydrocarbon solvent having the following characteristics: specific gravity, 0.8076; refractive index, 1.4483; flash point 110°C (230°F); K.F.No. 26.9; aniline point 77°C (170°F); aromatics, 10%; olefins, 5%, liquid paraffins, 85%; molecular weight (UOP 375-59), 205; initial/50%/final boiling pcints, 243°C/252°C/268°C (470°F/485°F/515°F).

Example 2

Example 1 is repeated using an aliphatic hydrocarbon ink resin in place of the rosin ester resin. The resin used in this example is a polymeric hydrocarbon resin having a ring-and-ball softening point of 165°C, an acid number of less than 1, a saponification number of less than 2, a bromine number of 21.5, and an iodine number of 113. It has a specific gravity of 1.05 at 25°C, a flash point exceeding 299°C, and a melt viscosity of 10/100/1000 poise at 237°C/208°C/189°C respectively (available as Piccovar® AB-165, Hercules

Incorporated). Essentially identical results to those of Example 1 are obtained.

Example 3-9

In order to evaluate other compounds, the methacryloxyethyl esters (Exs 3-7) and acryloxyethyl esters (Exs 8 and 9) of the acids in the following table were prepared in a manner similar to Example A. Cobalt naphthenate, 0.06% cobalt based on the weight of the ester, was added, and 6g of the liquid was stored in the dark in an aluminum dish having a diameter of about two inches (5 cm), and exposed to the air at room temperature (about 22° + 2°C). The materials were examined periodically. The time for development of a "skin" on the liquid sample is an indicia of the rate of cure the material would have in a formulated ink.

When examined three weeks later. the characterials had cured throughout to form a hard flim. This illustrates that even a minor amount or polyunsatunated ester is effective to induce complete curing. As indicated elsewhere herein, if the fatty acids comprise polyunsaturated ones, the peroxides formed initiate addition polymerization of the CH₂=C< groups of the mixed esters of the oleates, stearates, palmitates, when such groups are present in the reactive diluents.

A mixture of the methacryloxyethyl esters of stearic and palmitic acids is solid, but if liguefied, would no doubt act similarly to the oleates.