Patent Application
20180147874
This invention relates to laser markable articles, in particular to colour laser markable security documents.
Security cards are widely used for various applications such as identification purposes (ID cards) and financial transfers (credit cards). Such cards typically consist of a laminated structure consisting of various paper or plastic laminates and layers wherein some of them may carry alphanumeric data and a picture of the card holder. So called ‘smart cards’ can also store digital information by including an electronic chip in the card body. A principal objective of such security cards is that they cannot be easily modified or reproduced in such a way that the modification or reproduction is difficult to distinguish from the original.
Two techniques frequently used for preparing security documents are laser marking and laser engraving. In literature, laser engraving is often incorrectly used for laser marking. In laser marking, a colour change is observed by local heating of material, while in laser engraving material is removed by laser ablation.
Well known in the field of laser markable security documents is the use of laser markable polymeric supports. Laser marking produces a colour change from white to black in a laser markable support through carbonization of the polymer, usually polycarbonate as disclosed in e.g. EP-A 2181858 (AGFA GEVAERT).
During the past last years, there is an increased interest of using laser markable layers. The advantage of using a laser markable layer coated on a support instead of a laser markable support, is that a support can be used which has better physical properties than the laser markable supports, such as for example a higher flexibility than a polycarbonate support as disclosed in e.g. EP-A 2567825 (AGFA GEVAERT).
There is also an increased interest in using laser marking to produce coloured images in a security document. Therefore, laser markable layers are used which are composed of colour forming compounds (also called “leuco-dyes”) which can change from essentially colourless or pale-coloured to coloured when exposed to for example heat, such as disclosed in for example EP-A 2648920.
The colour laser markable layers may comprise an infrared absorbing dye (IR dye) or an infrared absorbing pigment (IR pigment), both absorbing the IR radiation and converting it into heat.
An advantage of using IR dyes is that the absorption spectrum of an IR dye tends to be narrower than that of an IR pigment. This allows the production of multicoloured articles and security documents from precursors having a plurality of laser markable layers containing different IR dyes and colour forming compounds. The IR dyes having a different maximum absorption wavelength can then be adressed by IR lasers with corresponding emmision wavelengths causing colour formation only in the laser markable layer of the adressed IR dye. Such multicolour articles have been disclosed in for example U.S. Pat. No. 4,720,449, EP-A 2719540 and EP-A 2719541.
A problem of colour laser markable materials comprising an IR dye and a leuco dye is often their poor daylight stability. When such materials, for example security documents, are exposed to daylight for a long time, a background stain becomes more and more pronounced.
Another disadvantage of colour laser markable materials disclosed in for example EP-A 2719541 is the fact that the colour laser markable layers comprising a leuco dye and an IR dye are prepared from non-aqueous coating solutions making their production more cumbersome regarding health and safety regulations.
Preferred embodiments of the present invention provide a colour laser markable article that has an improved daylight stability.
Further preferred embodiments of the present invention provide a colour laser markable article that may be produced in more safe and environmentally friendly conditions.
These advantages and benefits are realized by the laser markable article as defined below.
Further advantages and embodiments of the present invention will become apparent from the following description.
In
The terms polymeric support and foil, as used herein, mean a self-supporting polymer-based sheet, which may be associated with one or more adhesion layers, e.g. subbing layers. Supports and foils are usually manufactured through extrusion.
The term layer as used herein, is considered not to be self-supporting and is manufactured by coating it on a (polymeric) support or foil.
The term leuco dye as used herein refers to compounds which can change from essentially colourless or pale-coloured to coloured when irradiated with UV light, IR light and/or heated.
PET is an abbreviation for polyethylene terephthalate.
PETG is an abbreviation for polyethylene terephthalate glycol, the glycol indicating glycol modifiers which are incorporated to minimize brittleness and premature aging that occur if unmodified amorphous polyethylene terephthalate (APET) would be used in the production of cards.
PET-C is an abbreviation for crystalline PET, i.e. a biaxially stretched polyethylene terephthalate. Such a polyethylene terephthalate support has excellent properties of dimensional stability.
The definitions of security features correspond with the normal definition as adhered to in the Glossary of Security Documents—Security features and other related technical terms as published by the Consilium of the Council of the European Union on Aug. 25, 2008 (Version: v.10329.02.b.en) on its website: http://www.consilium.europa.eu/prado/EN/glossaryPopup.html.
The term security document precursor as used herein refers to the fact that one or more security features still have to be applied to the precursor, for example laser marking, in order to obtain the final security document.
The term alkyl means all variants possible for each number of carbon atoms in the alkyl group i.e. methyl, ethyl, for three carbon atoms: n-propyl and isopropyl; for four carbon atoms: n-butyl, isobutyl and tertiary-butyl; for five carbon atoms: n-pentyl, 1,1-dimethyl-propyl, 2,2-dimethylpropyl and 2-methyl-butyl etc.
The term alkoxy means all variants possible for each number of carbon atoms in the alkyl group i.e. methoxy, ethoxy, for three carbon atoms: n-propoxy and isopropoxy; for four carbon atoms: n-butoxy, isobutoxy and tertiary-butoxy etc.
The term aryloxy means Ar—C— wherein Ar is an optionally substituted aryl group.
Unless otherwise specified a substituted or unsubstituted alkyl group is preferably a C1 to C6-alkyl group.
Unless otherwise specified a substituted or unsubstituted alkenyl group is preferably a C2 to C6-alkenyl group.
Unless otherwise specified a substituted or unsubstituted alkynyl group is preferably a C2 to C6-alkynyl group.
Unless otherwise specified a substituted or unsubstituted aralkyl group is preferably a phenyl group or a naphthyl group including one, two, three or more C1 to C6-alkyl groups.
Unless otherwise specified a substituted or unsubstituted alkaryl group is preferably a C1 to C6-alkyl group including an aryl group, preferably a phenyl group or naphthyl group.
Unless otherwise specified a substituted or unsubstituted aryl group is preferably a substituted or unsubstituted phenyl group or naphthyl group.
A cyclic group includes at least one ring structure and may be a monocyclic- or polycyclic group, meaning one or more rings fused together.
A heterocyclic group is a cyclic group that has atoms of at least two different elements as members of its ring(s).The counterparts of heterocyclic groups are homocyclic groups, the ring structures of which are made of carbon only. Unless otherwise specified a substituted or unsubstituted heterocyclic group is preferably a five- or six-membered ring substituted by one, two, three or four heteroatoms, preferably selected from oxygen atoms, nitrogen atoms, sulphur atoms, selenium atoms or combinations thereof.
An alicyclic group is a non-aromatic homocyclic group wherein the ring atoms consist of carbon atoms.
The term heteroaryl group means a monocyclic- or polycyclic aromatic ring comprising carbon atoms and one or more heteroatoms in the ring structure, preferably, 1 to 4 heteroatoms, independently selected from nitrogen, oxygen, selenium and sulphur. Preferred examples of heteroaryl groups include, but are not limited to, pyridinyl, pyridazinyl, pyrimidyl, pyrazyl, triazinyl, pyrrolyl, pyrazolyl, imidazolyl, (1,2,3,)- and (1,2,4)-triazolyl, pyrazinyl, pyrimidinyl, tetrazolyl, furyl, thienyl, isoxazolyl, thiazolyl, isoxazolyl, and oxazolyl. A heteroaryl group can be unsubstituted or substituted with one, two or more suitable substituents. Preferably, a heteroaryl group is a monocyclic ring, wherein the ring comprises 1 to 5 carbon atoms and 1 to 4 heteroatoms.
The term substituted, in e.g. substituted alkyl group means that the alkyl group may be substituted by other atoms than the atoms normally present in such a group, i.e. carbon and hydrogen. For example, a substituted alkyl group may include a halogen atom or a thiol group. An unsubstituted alkyl group contains only carbon and hydrogen atoms.
Unless otherwise specified a substituted alkyl group, a substituted alkenyl group, a substituted alkynyl group, a substituted aralkyl group, a substituted alkaryl group, a substituted aryl, a substituted heteroaryl and a substituted heterocyclic group are preferably substituted by one or more substituents selected from the group consisting of methyl, ethyl, n-propyl, isopropyl, n-butyl, 1-isobutyl, 2-isobutyl and tertiary-butyl, ester, amide, ether, thioether, ketone, aldehyde, sulfoxide, sulfone, sulfonate ester, sulphonamide, —Cl, —Br, —I, —OH, —SH, —CN and —NO2.
The laser markable article according to a preferred embodiment of the present invention comprises at least a first and a second laser markable layer comprising respectively a first infrared dye IR-1 having an absorption maximum in the infrared region λmax(IR-1) and a second infrared dye IR-2 having an absorption maximum in the infrared region λmax(IR-2), characterized in that the colour laser markable layers further comprise a Diffusion Hindered Molecular Assembly (DHMA) which contains a leuco dye.
The diffusion of the leuco dye in the DHMA is limited to such an extent that before exposure to IR radiation substantially no colour formation occurs. The limited diffusion of the leuco dye results in substantially no reaction of the leuco dye with for example acid present in the laser markable layer.
In a preferred embodiment the DHMA is a capsule composed of a polymeric shell surrounding a core which contains a leuco dye.
In another preferred embodiment the DHMA is a polymer particle charged with a leuco dye.
Another preferred embodiment of the DHMA is a Composite Particle Dispersion containing a leuco dye.
The colour laser markable layers are preferably prepared from aqueous coating solutions.
The infrared dyes may be solubilized or dispersed into the aqueous coating solutions. Preferably however, the infrared dyes are also present in the laser markable layers as part of a DHMA.
DHMA's containing both a leuco dye and an IR dye or different DHMA's containing respectively a leuco dye and an infrared dye may be used in preparing the laser markable layers.
DHMA's containing more than one leuco dye may be used to optimize the colour obtained upon laser marking.
Upon absorption of infrared radiation, the infrared dye converts that radiation into heat. The heat then disrupts the Diffusion Hindered Molecular Assemblies whereupon the leuco dye comes into reactive contact with a so-called developer which then triggers the colour formation.
For example in the embodiment wherein the Diffusion Hindered Molecular Assembly is a capsule composed of a polymeric shell surrounding a core which contains a leuco dye, the heat breaks open de capsules, whereupon the leuco dye comes into reactive contact with a developer which is present in the laser markable layer resulting in colour formation.
The laser markable layers may further comprise a binder, an acid scavenger, and other ingredients to further optimize its properties.
The laser markable layers may be provided onto a support by co-extrusion or any conventional coating technique, such as dip coating, knife coating, extrusion coating, spin coating, spray coating, slide hopper coating and curtain coating. Preferably the laser markable layer is coated with a slide hopper coater or a curtain coater.
The laser markable layers may also be provided onto a support by inkjet printing. Using inkjet printing is preferred when only a part or several parts of a support has to be provided with a laser markable layer.
The dry thickness of the laser markable layers is preferably between 1 and 50 g/m2, more preferably between 2 and 25 g/m2, and most preferably between 3 and 15 g/m2.
A preferred laser markable article includes three laser markable layers, a first laser markable layer containing a first infrared dye IR-1 having an absorption maximum in the infrared region λmax(IR-1), a second laser markable layer containing a second infrared dye IR-2 having an absorption maximum in the infrared region λmax(IR-2), and a third laser markable layer containing a third infrared dye IR-3 having an absorption maximum in the infrared region λmax(IR-3), wherein the colour laser markable layers further comprise a Diffusion Hindered Molecular Assembly which contains a leuco dye.
In a preferred colour laser markable article, the conditions a) and b) are fulfilled:
λmax(IR-1)>λmax(IR-2)>λmax(IR-3); and a)
λmax(IR-1)>1100 nm and λmax(IR-3)<1000 nm. b)
In a particularly preferred colour laser markable article the condition c) is also fulfilled:
λmax(IR-2) differs by at least 60 nm from λmax(IR-1) and λmax(IR-3). c)
In another preferred colour laser markable article, λmax(IR-3)≥830 nm and λmax(IR-1)≥1125 nm.
In a preferred embodiment, the colour laser markable article comprises three colour laser markable layers each including a different leuco dye for forming a colour having an absorption maximum of respectively λmax(VIS-1), λmax(VIS-2), and λmax(VIS-3) in the visible spectrum of 400 nm to 700 nm, wherein all the relations a) to c) are fulfilled:
400 nm<λmax(VIS-1)<500 nm; a)
500 nm<λmax(VIS-2)<600 nm; and b)
600 nm<λmax(VIS-3)<700 nm. c)
A preferred laser markable material includes the laser markable layers as described above applied on a support. A preferred support is a polymeric support, a particularly preferred support is a transparent polymeric support.
The laser markable article may in addition to the laser markable layers contain additional layers, such as for example subbing layers to improve the adhesion towards a support, an outer layer that is suitable as a receiver layer for dyes applied by thermal dye sublimation or inkjet printing, or intermediate layers between the laser markable layers to prevent colour contamination.
In a preferred embodiment, the laser markable article is provided, for example laminated, on a core support, preferably on both sides of the core support (see
In a preferred embodiment, the colour laser marked document is a security document, preferably selected from the group consisting of a passport, a personal identification card and a product identification document.
The colour laser markable document preferably also contains electronic circuitry, more preferably the electronic circuitry includes a RFID chip with an antenna and/or a contact chip. The security document is preferably a “smart card”, meaning an identification card incorporating an integrated circuit. In a preferred embodiment the smart card includes a radio frequency identification or RFID-chip with an antenna. Inclusion of electronic circuitry makes forgery more difficult.
The colour laser markable document preferably has a format as specified by ISO 7810. ISO 7810 specifies three formats for identity cards: ID-1 with the dimensions 85.60 mm×53.98 mm, a thickness of 0.76 mm is specified in ISO 7813, as used for bank cards, credit cards, driving licences and smart cards; ID-2 with the dimensions 105 mm×74 mm, as used in German identity cards, with typically a thickness of 0.76 mm; and ID-3 with the dimensions 125 mm×88 mm, as used for passports and visa's. When the security cards include one or more contactless integrated circuits then a larger thickness is tolerated, e.g. 3 mm according to ISO 14443-1.
In another preferred embodiment, the colour laser markable document is a product identification document which is usually attached to the packaging material of the product or to the product itself. The product identification document not only allows to verify the authenticity of the product, but also to maintain the attractive look of a product (packaging).
In a particularly preferred embodiment of the present invention, the Diffusion Hindered Molecular Assembly is a capsule having a polymeric shell surrounding a core containing a leuco dye and preferably an infrared dye.
Upon exposure, a rupture of the capsule, for example by heat produced by the sensitizer upon absorption of IR radiation, results in a reaction between the leuco dye and a developer which then trigger colour formation.
The morphology of capsules and their preparation methods have been reviewed, for example, by Jyothi Sri. S in the International Journal of Pharma and Bio Sciences (Vol. 3, Issue 1, January-March 2012).
The capsules typically have an average particle size between 3 and 5 μm, or smaller. Such capsules are often referred to as microcapsules. More preferably, the average particle size of the capsules is from 0.05 to 2 μm, more preferably from 0.10 to 1 μm.
The capsules may have different morphologies, dependent on the preparation method of the capsules. For example mononuclear capsules have a shell around a core while polynuclear capsules have multiple cores enclosed within the shell. Matrix encapsulation refers to a core material which is homogeneously distributed into the shell.
Hydrophilic polymers, surfactants and/or polymeric dispersants may be used to obtain stable dispersions of the capsules in an aqueous medium and to control the particle size and the particle size distribution of the capsules.
In a preferred embodiment, the capsules are dispersed in the aqueous medium using a dispersing group covalently bonded to the polymeric shell. The dispersing group is preferably selected from a group consisting of a carboxylic acid or salt thereof, a sulfonic acid or salt thereof, a phosphoric acid ester or salt thereof, a phosphonic acid or salt thereof, an ammonium group, a sulfonium group, a phosphonium group and a polyethylene oxide group.
The dispersing groups stabilize the aqueous dispersion by electrostatic stabilization. For example, a slightly alkaline aqueous medium will turn the carboxylic acid groups covalently bonded to the polymeric shell into ionic groups, whereafter the negatively charged capsules have no tendency to agglomerate. If sufficient dispersing groups are covalently bonded to the polymeric shell, the capsule becomes a so-called self-dispersing capsule. Other dispersing groups such as sulfonic acid groups tend to be dissociated even in acid aqueous medium and thus do not require the addition of an alkali.
The dispersing group can be used in combination with a polymeric dispersant in order to accomplish steric stabilization. For example, the polymeric shell may have covalently bonded carboxylic acid groups that interact with amine groups of a polymeric dispersant. However, in a more preferred embodiment, no polymeric dispersant is used and dispersion stability is accomplished solely by electrostatic stabilization.
The capsules may also be stabilized by solid particles which adsorb onto the shell. Preferred solid particles are colloidal silica.
There is no real limitation on the type of polymer used for the polymeric shell of the capsule. Preferably, the polymer used in the polymeric shell is crosslinked. By crosslinking, more rigidity is built into the capsules allowing a broader range of temperatures and pressures for handling the colour laser markable article.
Preferred examples of the polymeric shell material include polyureas, polyurethanes, polyesters, polycarbonates, polyamides, melamine based polymers and mixtures thereof, with polyureas and polyurethanes being especially preferred.
Capsules can be prepared using both chemical and physical methods. Suitable encapsulation methodologies include complex coacervation, liposome formation, spray drying and polymerization methods.
In a preferred embodiment of the present invention, preferably a polymerization method is used as it allows the highest control in designing the capsules. More preferably interfacial polymerization is used to prepare the capsules used in the invention. This technique is well-known and has recently been reviewed by Zhang Y. and Rochefort D. (Journal of Microencapsulation, 29(7), 636-649 (2012) and by Salitin (in Encapsulation Nanotechnologies, Vikas Mittal (ed.), chapter 5, 137-173 (Scrivener Publishing LLC (2013)).
Interfacial polymerisation is a particularly preferred technology for the preparation of capsules according to a preferred embodiment of the present invention. In interfacial polymerization, such as interfacial polycondensation, two reactants meet at the interface of the emulsion droplets and react rapidly.
In general, interfacial polymerisation requires the dispersion of an oleophilic phase in an aqueous continuous phase or vice versa. Each of the phases contains at least one dissolved monomer (a first shell component) that is capable of reacting with another monomer (a second shell component) dissolved in the other phase. Upon polymerisation, a polymer is formed that is insoluble in both the aqueous and the oleophilic phase. As a result, the formed polymer has a tendency to precipitate at the interface of the oleophilic and aqueous phase, hereby forming a shell around the dispersed phase, which grows upon further polymerisation. The capsules according to a preferred embodiment of the present invention are preferably prepared from an oleophilic dispersion in an aqueous continuous phase.
Typical polymeric shells, formed by interfacial polymerisation are selected from the group consisting of polyamides, typically prepared from di- or oligoamines as first shell component and di- or poly-acid chlorides as second shell component; polyurea, typically prepared from di- or oligoamines as first shell component and di- or oligoisocyanates as second shell component; polyurethanes, typically prepared from di- or oligoalcohols as first shell component and di- or oligoisocyanates as second shell component; polysulfonamides, typically prepared from di- or oligoamines as first shell component and di- or oligosulfochlorides as second shell component; polyesters, typically prepared from di- or oligoalcohols as first shell component and di- or oligo-acid chlorides as second shell component; and polycarbonates, typically prepared from di- or oligoalcohols as first shell component and di- or oligo-chloroformates as second shell component. The shell can be composed of combinations of these polymers.
In a further embodiment, polymers, such as gelatine, chitosan, albumin and polyethylene imine can be used as first shell components in combination with a di- or oligo-isocyanate, a di- or oligo acid chloride, a di- or oligo-chloroformate and an epoxy resin as second shell component.
In a particularly preferred embodiment, the shell is composed of a polyurethane, a polyurea or a combination thereof.
In a further preferred embodiment, a water immiscible solvent is used in the dispersion step, which is removed by solvent stripping before or after the shell formation. In a particularly preferred embodiment, the water immiscible solvent has a boiling point below 100° C. at normal pressure. Esters are particularly preferred as water immiscible solvent. A preferred organic solvent is ethyl acetate, because it also has a low flammability hazard compared to other organic solvents.
A water immiscible solvent is an organic solvent having low miscibility in water. Low miscibility is defined as any water solvent combination forming a two phase system at 20° C. when mixed in a one over one volume ratio.
The method for preparing a dispersion of capsules preferably includes the following steps:
Capsules containing an infrared dye in its core can be made in an analogous way by replacing the leuco dye in step a) of the method described above by an infrared dye.
Capsules containing both a leuco dye and an infrared dye can be prepared by using a leuco dye and an infrared dye in step a) of the method described above.
Capsules containing more than one leuco dye may be used to optimize the colour obtained upon laser marking.
The capsule containing a leuco dye and preferably an infrared dye can then be dispersed in an aqueous medium.
In another preferred embodiment of the present invention, the Diffusion Hindered Molecular Assembly is a polymer particle charged with a leuco dye and/or an infrared dye.
The polymer particles are preferably latex particles, i.e. polymer particles with which a stable aqueous dispersion may be formed. The polymeric particles are preferably nanoparticles. The term “polymer nanoparticles” means that at least part of the polymer particles has a particle diameter less than 1 μm as determined by Laser Diffraction. The polymer nanoparticles preferably have an average diameter smaller than 1 μm.
There is no real limitation on the chemical nature of the polymer particles. Suitable examples of the polymer of the polymer particles include a vinyl polymer and a condensed polymer (e.g., an epoxy resin, polyester, polyurethane, polyamide, cellulose, polyether, polyurea, polyimide, and polycarbonate). Among the above, a vinyl polymer and a polyurethane polymer or copolymer are particularly preferred.
The polymer particles are preferably self-dispersible polymer particles. In preparing a self-dispersing polymer latex, preferably a monomer is used selected from the group consisting of a carboxylic acid monomer, a sulfonic acid monomer, and a phosphoric acid monomer.
Specific examples of the unsaturated carboxylic acid monomer include acrylic acid, methacrylic acid, crotonic acid, itaconic acid, maleic acid, fumaric acid, citraconic acid, and 2-methacryloyloxy methylsuccinic acid. Specific examples of the unsaturated sulfonic acid monomer include styrene sulfonic acid, 2-acrylamido-2-methyl propane sulfonic acid, 3-sulfopropyl (meth)acrylate, and bis-(3-sulfopropyl)-itaconate. Specific examples of the unsaturated phosphoric acid monomer include vinyl phosphoric acid, vinyl phosphate, and bis(methacryloxyethyl)phosphate. Such monomers may be incorporated into polyurethane copolymers which include a (meth)acrylate polymeric chain.
For polyurethane polymer particles, the self-dispersing group may be incorporated via a diol and/or a diamine having any of phosphate group, a sulfonic acid group, a N,N-disubstituted amino group, a carboxyl group, a neutralized phosphate group, a neutralized sulfonic acid group, a neutralized N,N-disubstituted amino group and a neutralized carboxyl group. Specific examples thereof include trimethylolpropane monophosphate, trimethylolpropane monosulfate, a polyester diol where at least a part of the dibasic acid component is sodium sulfosuccinate or sodium sulfo-isophthalate, N-methyldiethanolamine, diaminocarboxylic acid such as lysine, cystine or 3,5-diaminocarboxylic acid, 2,6-dihydroxybenzoic acid, 3,5-dihydroxy-benzoic acid, dihydroxyalkylalkanoic acid such as 2,2-bis(hydroxymethyl)propionic acid, 2,2-bis(hydroxyethyl)propionic acid, 2,2-bis(hydroxypropyl)-propionic acid, bis(hydroxymethyl)acetic acid or 2,2-bis(hydroxymethyl)butanoic acid, bis(4-hydroxyphenyl)-acetic acid, 2,2-bis(4-hydroxyphenyl)pentanoic acid, tartaric acid, N,N-hydroxyethylglycine, N,N-bis(2-hydroxyethyl)-3-carboxypropionamide and a carboxyl group-containing polycaprolactone diol where a lactone compound such as ε-caprolactone is added to dihydroxyalkylalkanoic acid.
Manufacturing methods for polyurethane polymer or copolymer particles are well-known. Generally a compound having a salt group, a polyisocyanate compound having two or more isocyanate groups, and a polyol compound are reacted to form a polyurethane polymer. Then the salt group is neutralized at 50° C. or lower using a basic compound. The obtained polyurethane polymer or copolymer is then dispersed in an aqueous medium followed by evaporation of organic solvent.
Examples of the above di- and higher functional polyisocyanate compound include an aliphatic diisocyanate such as 1,6-hexamethylene diisocyanate, 2,2,4-trimethyl-hexamethylene diisocyanate or lysine diisocyanate; an aliphatic polyisocyanate such as a trimer of the above aliphatic diisocyanate or an adduct of low-molecular triol with the above aliphatic isocyanate; an alicyclic diisocyanate such as isophorone diisocyanate, hydrogenated MDI, hydrogenated tolylene diisocyanate, methyl-cyclohexylene diisocyanate, isopropylidenecyclohexyl-4,4′-diisocyanate or norbornene diisocyanate; an alicyclic polyisocyanate such as a trimer of the above alicyclic diisocyanate or an adduct of low-molecular triol with the above alicyclic isocyanate; an aromato-aliphatic diisocyanate such as xylylene diisocyanate; an aromatic alicyclic polyisocyanate such as a trimer of xylylene diisocyanate or an adduct of low-molecular triol with the above aromato-aliphatic isocyanate; an aromatic diisocyanate such as 4,4′-diphenylmethane diisocyanate or tolylene diisocyanate; an aromatic polyisocyanate such as triphenylmethane triisocyanate, a trimer of the above aromatic diisocyanate or an adduct of low-molecular triol with the above aromatic isocyanate; a tri- or higher functional polyisocyanate such as polymethylene polyphenyl isocyanate; and a polyisocyanate compound having a carbodiimide group such as Cosmonate LL (manufactured by Mitsui Chemical; a mixture of carbodiimidated 4,4′-diphenylmethane diisocyanate with 4,4′-diphenyl-methane diisocyanate) or Carbodilide V-05 (manufactured by Nisshinbo; a terminal aliphatic polyisocyanate compound having a polycarbodiimide group). It is also possible that two or more of the above polyisocyanate compounds are mixed and used.
Examples of the above polyol compound include ethylene glycol, propylene glycol, diethylene glycol, cyclohexane-1,4-dimethanol, 1,3-butylene glycol, 1,4-butylene glycol, neopentyl glycol, 1,6-hexanediol, 3-methyl-1,5-pentanediol, 2-ethyl-1,3-hexanediol, 2-butyl-2-ethyl-1,3-propanediol, 2-methyl-1,8-octanediol, 1,9-nonanediol, cyclohexyl dimethanol, bisphenol A, bisphenol F, hydrogenated bisphenol A, hydrogenated bisphenol F, castor oil modified diol and castor oil modified polyol.
For charging a leuco dye and/or infrared dye onto polymer nanoparticles, the leuco dye and/or infrared dye are first dissolved in a water-immiscible organic solvent having a boiling point of lower than 100° C. This solvent mixture is then finely dispersed in water or an aqueous medium, for example by a homogenizer, a microfluidizer or very high speed stirring in order to form an “oil-in-water” emulsion. This emulsion is then under stirring added to an aqueous medium containing dispersed polymer particles. The organic solvent is then distilled therefrom so that the leuco dye and/or infrared dye are transferred from the organic solvent phase to the polymer particles as they becomes insoluble in the aqueous phase.
In order to obtain more concentrated charged polymer nanoparticle dispersions, the following method is used. The leuco dye and/or infrared dye are first dissolved in a water-immiscible organic solvent having a boiling point of lower than 100° C. This solvent mixture is then added to an aqueous medium containing dispersed polymer nanoparticles under very high speed stirring or by using a homogenizer or a microfluidizer. The organic solvent is distilled there from so that the leuco dye and/or infrared dye are transferred from the organic solvent phase to the polymer nanoparticles as they become insoluble in the aqueous phase.
Examples of an organic solvent having boiling point of lower than 100° C. include acetone, methyl ethyl ketone, tetrahydrofuran, ethyl ether, n-propyl ether, isopropyl ether, n-butyl methyl ether, tert-butyl methyl ether, n-butyl ethyl ether, tert-butyl ethyl ether, ethyl acetate, isopropyl acetate, methyl propionate and acetonitrile although they are non-limitative. In addition, each of them may be used solely or they may be used jointly by mixing them. Among those ones, ethyl acetate and methyl ethyl ketone are preferred.
In another embodiment of the present invention, the Diffusion Hindered Molecular Assembly is a Composite Particle Dispersion of a leuco dye and/or an infrared dye. The term “Composite Particle Dispersion” of a leuco dye and/or infrared dye as used herein means a dispersion of the leuco dye and/or infrared dye in an aqueous medium. The term “Composite Particle Dispersion” refers to the fact that the particles may contain, in addition to the leuco dye, other ingredients such as surfactants, polymeric resins, polymeric dispersants, or water-immiscible organic solvents.
A preferred embodiment of such a Composite Particle Dispersion of a leuco dye is prepared by first dissolving the leuco dye in organic solvent. The organic solvent may be a volatile organic solvent, a non-volatile organic solvent or preferably a mixture of a volatile and non-volatile organic solvent. This solution is then added to an aqueous medium, preferably under very high speed stirring or by using a homogenizer or a microfluidizer. When a volatile organic solvent is present, it is preferably removed from the system, preferably by heating. When a non-volatile organic solvent is used, the result is an oil-in-water emulsion wherein the leuco dye is present in the oil phase of the emulsion. This oil-in-water emulsion is however also referred to herein as a composite particle dispersion.
The organic solvent is a liquid at room temperature, water immiscible and capable of dissolving the leuco dye. Low miscibility is defined as any water solvent combination forming a two phase system at 20° C. when mixed in a one over one volume ratio.
Examples of suitable volatile organic solvent are the organic solvents having a boiling point below 100° C. described above for preparing the Capsules and the Polymer particles containing a leuco dye.
Examples of the non-volatile organic solvents are phosphates, phthalates, (meth)acrylates, fatty acid amides, alkylated biphenyls, alkylated terphenyls, alkylated naphthalenes, diarylethanes, chlorinated paraffins, alcohol solvents, phenolic solvents, ether solvents, monoolefin solvents and epoxy solvents. Preferred examples are high boiling solvents such as tricresyl phosphate, trioctyl phosphate, octyldiphenyl phosphate, tricyclohexyl phosphate, dibutylphthalate, dioctyl phthalate, dilauryl phthalate, dicyclohexyl phthalate, diethylene glycol benzoate, dioctyl cebacate, dibutyl cebacate, dioctyl adipate, trioctyl trimellitate, acetyltriethyl citrate, octyl maleate, dibutyl maleate, isoamylbiphenyl, chlorinated paraffin, diisopropylnaphthalene, 1,1′-ditolylethane, monoisopropylbiphenyl, diisopropylbiphenyl, 2,4-ditertiary-amylphenol, N,N-dibutyl-2-butoxy-5-tertiary-octylaniline, 2-ethylhexyl hydroxybenzoate, and polyethylene glycol.
The non-volatile organic solvent described above may be at least partially replaced by a non-crystalline polymer.
The distillation of the organic solvent having a boiling point of lower than 100° C. is preferably carried out under reduced pressure to avoid decomposition of the leuco dye. Under reduced pressure, the temperature may be lowered, for example to 70° C. or lower, during the distillation step.
Hydrophilic polymers, surfactants and/or polymeric dispersants may be used to obtain stable dispersions of the composite particles in an aqueous medium and to control the particle size and the particle size distribution of the composite particle.
Polymeric dispersants typically have anchoring groups, which adsorb on the surface of the composite particles. The polymeric dispersant added to the aqueous medium containing the composite particles preferably includes one more functional groups selected from a carboxylic acid or salt thereof, a sulfonic acid or salt thereof, a phosphoric acid ester or salt thereof, a phosphonic acid or salt thereof, an ammonium group, a sulfonium group, a phosphonium group and a polyethylene oxide group. In a more preferred embodiment, the polymeric dispersant added to the aqueous medium containing the composite particles preferably includes one more functional groups selected from the group consisting of: —COO−M+, —SO3−M+, —O—PO3−M+, —O—SO3−M+, —PO3−M+; wherein M+ represents H+ or a cation selected from the group consisting of Na+, Li+, K+ and NH4+.
When surfactants are used, non-ionic and anionic surfactants are preferred.
Suitable non-ionic surfactants are disclosed in WO2005/111727 page 7, ln.24 to page 8, ln.5).
Suitable anionic surfactants are disclosed in WO2005/111727 page 6, ln.32 to page 7, ln.23).
These surfactants may be used in combination with a polymeric dispersant described above.
To obtain the right colour, for example a specific blue colour, typically more than one leuco dye is used. For each leuco dye, a different Composite Particle Dispersion may be prepared as described above. However, it may be advantageous, especially regarding the stability of the dispersions, to make a single Composite Particle Dispersion containing the different leuco dyes.
A Composite Particle Dispersion of an infrared dye may be prepared in the same way as described above for a leuco dye.
A Composite Particle Disperson of both a leuco dye and an infrared dye may be prepared by dissolving both a leuco dye and an infrared dye in the organic solvent and then further carrying out the preparation method described above.
Upon absorption of infrared radiation, the infrared dye converts that radiation into heat. The heat than disrupts the Diffusion Hindered Molecular Assemblies whereupon the leuco dye comes into reactive contact with a so-called developer which then triggers the colour formation.
Various electron accepting substances may be used as developers in the present invention. Examples thereof include phenolic compounds, organic or inorganic acidic compounds and esters or salts thereof.
Specific examples include bisphenol A; tetrabromobisphenol A; gallic acid; salicylic acid; 3-isopropyl salicylate; 3-cyclohexyl salicylate; 3-5-di-tert-butylsalicylate; 3,5-di-α-methyl benzyl salicylate; 4,4′-isopropylidenediphenol; 1,1′-isopropylidene bis(2-chlorophenol); 4,4′-isopropylene bis(2,6-dibromo-phenol); 4,4′-isopropylidene bis(2,6-dichlorophenol); 4,4′-isopropylidene bis(2-methyl phenol); 4,4′-isopropylidene bis(2,6-dimethyl phenol); 4,4′-isopropylidene bis(2-tert-butyl phenol); 4,4′-sec-butylidene diphenol; 4,4′-cyclohexylidene bisphenol; 4,4′-cyclohexylidene bis(2-methyl phenol); 4-tert-butyl phenol; 4-phenyl phenol; 4-hydroxy diphenoxide; α-naphtholnaphthol; β-naphtol; 3,5-xylenol; thymol; methyl-4-hydroxybenzoate; 4-hydroxy-acetophenone; novolak phenol resins; 2,2′-thio bis(4,6-dichloro phenol); catechol; resorcin; hydroquinone; pyrogallol; fluoroglycine; fluoroglycine carboxylate; 4-tert-octyl catechol; 2,2′-methylene bis(4-chlorophenol); 2,2′-methylene bis(4-methyl-6-tert-butyl phenol); 2,2′-dihydroxy diphenyl; ethyl p-hydroxybenzoate; propyl p-hydroxybenzoate; butyl p-hydroxy-benzoate; benzyl p-hydroxybenzoate; p-hydroxybenzoate-p-chlorobenzyl; p-hydroxybenzoate-o-chlorobenzyl; p-hydroxybenzoate-p-methylbenzyl; p-hydroxybenzoate-n-octyl; benzoic acid; zinc salicylate; 1-hydroxy-2-naphthoic acid; 2-hydroxy-6-naphthoic acid; 2-hydroxy-6-zinc naphthoate; 4-hydroxy diphenyl sulphone; 4-hydroxy-4′-chloro diphenyl sulfone; bis(4-hydroxy phenyl)sulphide; 2-hydroxy-p-toluic acid; 3,5-di-tert-zinc butyl salicylate; 3,5-di-tert-tin butyl salicylate; tartaric acid; oxalic acid; maleic acid; citric acid; succinic acid; stearic acid; 4-hydroxyphthalic acid; boric acid; thiourea derivatives; 4-hydroxy thiophenol derivatives; bis(4-hydroxyphenyl) acetate; bis(4-hydroxyphenyl)ethyl acetate; bis(4-hydroxyphenyl)acetate-n-propyl; bis(4-hydroxyphenyl) acetate-n-butyl; bis(4-hydroxyphenyl)phenyl acetate; bis(4-hydroxyphenyl)benzyl acetate; bis(4-hydroxyphenyl)phenethyl acetate; bis(3-methyl-4-hydroxyphenyl)acetate; bis(3-methyl-4-hydroxy-phenyl)methyl acetate; bis(3-methyl-4-hydroxyphenyl)acetate-n-propyl; 1,7-bis(4-hydroxyphenylthio)3,5-dioxaheptane; 1,5-bis(4-hydroxy-phenylthio)3-oxaheptane; 4-hydroxy phthalate dimethyl; 4-hydroxy-4′-methoxy diphenyl sulfone; 4-hydroxy-4′-ethoxy diphenyl sulfone; 4-hydroxy-4′-isopropoxy diphenyl sulfone; 4-hydroxy-4′-propoxy diphenyl sulfone; 4-hydroxy-4′-butoxy diphenyl sulfone; 4-hydroxy-4′-isopropoxy diphenyl sulfone; 4-hydroxy-4′-sec-butoxy diphenyl sulfone; 4-hydroxy-4′-tert-butoxy diphenyl sulfone; 4-hydroxy-4′-benzyloxy diphenyl sulfone; 4-hydroxy-4′-phenoxy diphenyl sulfone; 4-hydroxy-4′-(m-methyl benzoxy)diphenyl sulfone; 4-hydroxy-4′-(p-methyl benzoxy)diphenyl sulfone; 4-hydroxy-4′-(o-methyl benzoxy)diphenyl sulfone; 4-hydroxy-4′-(p-chloro benzoxy)diphenyl sulfone and 4-hydroxy-4′-oxyaryl diphenyl sulfone.
A preferred developer is a metal salt of salicylate, for example zinc salicylate. A particularly preferred zinc salicylate is zinc 3,5-bis(α-methylbenzyl) salicylate.
The developer may be present in the continuous phase of the laser markable layer or may also be added as a Diffusion Hindered Molecular Assembly of the developer, for example as a capsule containing the developer in its core.
Thermal acid generating compounds are compounds that generate an acid at higher temperatures, for example upon exposure to infrared radiation when an infrared absorbing dye is present which converts the infrared radiation into heat. Such thermal acid generating compounds may also be used in the present invention to catalyze or amplify the colour formation.
Because these compounds become a developer, i.e. an acid, upon exposure to infrared radiation, they may be present in a DHMA together with a leuco dye. However, they may also be present in the laser markable layer, outside the DHMA.
Preferred thermal acid generating compounds have a structure according to Formula (I) or Formula (II):
wherein
Suitable alkyl groups include 1 or more carbon atoms such as for example C1 to C22-alkyl groups, more preferably C1 to C12-alkyl groups and most preferably C1 to C6-alkyl groups. The alkyl group may be lineair or branched such as for example methyl, ethyl, propyl (n-propyl, isopropyl), butyl (n-butyl, isobutyl, t-butyl), pentyl, 1,1-dimethyl-propyl, 2,2-dimethylpropyl and 2-methyl-butyl, or hexyl.
Suitable cyclic alkyl groups include cyclopentyl, cyclohexyl or adamantyl.
Suitable heterocyclic alkyl groups include tetrahydrofuryl, piperidinyl, pyrrolidinyl, dioxyl, tetrahydrothiophenyl, silolanyl, or thianyl oxanyl.
Suitable aryl groups include for example phenyl, naphthyl, benzyl, tolyl, ortho- meta- or para-xylyl, anthracenyl or phenanthrenyl.
Suitable heteroaryl groups include monocyclic- or polycyclic aromatic rings comprising carbon atoms and one or more heteroatoms in the ring structure. Preferably 1 to 4 heteroatoms independently selected from nitrogen, oxygen, selenium and sulphur and/or combinations thereof. Examples include pyridyl, pyrimidyl, pyrazoyl, triazinyl, imidazolyl, (1,2,3,)- and (1,2,4)-triazolyl, tetrazolyl, furyl, thienyl, isoxazolyl, thiazolyl and carbazoyl.
Suitable alkoxy groups include those containing from 1 to 18, preferably 2 to 8 carbon atoms, such as ethoxide, propoxide, isopropoxide, butoxide, isobutoxide and tert-butoxide.
Suitable aryloxy groups include phenoxy and naphthoxy.
The alkyl, (hetero)cyclic alkyl, aralkyl, (hetero)aryl, alkoxy, (hetero)cyclic alkoxy, or (hetero)aryloxy groups may include one or more substituents. The optional substituents are preferably selected from an alkyl group such as a methyl, ethyl, n-propyl, isopropyl, n-butyl, 1-isobutyl, 2-isobutyl and tertiary-butyl group; an ester, amide, ether, thioether, ketone, aldehyde, sulfoxide, sulfone, sulfonate ester or sulphonamide group, a halogen such as fluorine, chlorine, bromine or iodine, —OH, —SH, —CN and —NO2, and/or combinations thereof.
R1 preferably represents a C1 to C22-alkyl group, an aliphatic alkoxide group containing 2 to 8 carbons, a phenyl group or a tolyl group. R1 most preferably represents a tolyl group.
R2 preferably represents a C1 to C22-alkyl group or a (hetero)cyclic alkyl group. R2 most preferably represents a cyclohexyl group.
R3 preferably represents a C1 to C22-alkyl group, an aliphatic alkoxide group containing 2 to 8 carbons or a benzyl group.
In a preferred embodiment, R4 and R5 independently represent a C1 to C22-alkyl group. In a preferred embodiment, R4 and R5 represent independently an isobutyl, t-butyl, isopropyl, 2-ethylhexyl or a linear C2 to C8-alkyl group.
The compound used in a preferred embodiment of the present invention can be a monomer, an oligomer (i.e. a structure including a limited amount of monomers such as two, three or four repeating units) or a polymer (i.e. a structure including more than four repeating units).
The compound used in a preferred embodiment of the present invention contains at least one moiety according to Formula I and/or Formula II, preferably 1 to 150 moieties according to Formula I and/or Formula II. According to a preferred embodiment, the compound according to Formula I or Formula II may be present in a side chain of a polymer
In the embodiment wherein the compound according to Formula I or Formula II is present in the side chain of a polymer, the following moiety (Formula III, IV or V) is preferably attached to the polymer:
wherein
In the embodiment wherein the compound according to Formula I is present in the side chain of a polymer, the polymer is more preferably obtained from the coupling of a polymer or copolymer bearing side chains with alcohol groups and a sulfonyl chloride.
In the embodiment wherein the compound according to Formula I is present in the side chain of a polymer, the polymer is most preferably obtained from the coupling of a polymer or copolymer bearing side chains with alcohol groups and tosyl chloride. Useful polymers bearing side chains with alcohol include for example polyvinyl alcohol, polyvinyl butyral, cellulose derivatives, homo- and copolymers of 2-hydroxyethyl methacrylate, 2-hydroxyethyl acrylate, polysiloxane derivatives such as copolymers of hydroxyalkyl-methylsiloxane, and novolac resins.
Examples of acid generating compounds according to the present invention are shown in Table 1.
Other classes of photo- and thermal acid generators are iodonium salts, sulfonium salts, ferrocenium salts, sulfonyl oximes, halomethyl triazines, halomethylarylsulfone, α-haloacetophenones, sulfonate esters, t-butyl esters, allyl substituted phenols, t-butyl carbonates, sulfate esters, phosphate esters and phosphonate esters.
The infrared dyes in the different colour laser markable layers of the colour laser markable article differ in wavelength of maximum absorption λmax so that they can be addressed by different infrared lasers with corresponding wavelengths causing colour formation only in the colour laser markable layer of the addressed infrared dye.
The colour laser markable article according to a preferred embodiment of present invention comprises at least two, preferably at least three, colour laser markable layers having different infrared dyes and different leuco dyes. The different infrared dyes have an absorption maximum in the infrared region which differs preferably by at least 60 nm, more preferably at least 80 nm and most preferably at least 90 nm.
Suitable examples of infrared dyes (IR dyes) include, but are not limited to, polymethyl indoliums, metal complex IR dyes, indocyanine green, polymethine dyes, croconium dyes, cyanine dyes, merocyanine dyes, squarylium dyes, chalcogenopyryloarylidene dyes, metal thiolate complex dyes, bis(chalcogenopyrylo)polymethine dyes, oxyindolizine dyes, bis(aminoaryl)polymethine dyes, indolizine dyes, pyrylium dyes, quinoid dyes, quinone dyes, phthalocyanine dyes, naphthalocyanine dyes, azo dyes, (metalized) azomethine dyes and combinations thereof.
Preferred infrared dyes having an absorption maximum of more than 1100 nm are those disclosed in EP-A 2722367, paragraphs [0044] to [0083] and the unpublished EP-A 14166498.7 (filed on Apr. 30, 2014).
Infrared dyes having an absorption maximum between 1000 nm and 1100 nm are preferably selected from the group consisting of quinoline dyes, indolenine dyes, especially a benzo[cd]indoline dye. A particularly preferred infrared dye is 5-[2,5-bis[2-[1-(1-methylbutyl)-benz[cd]indol-2(1H)-ylidene]ethylidene]cyclopentylidene]-1-butyl-3-(2-methoxy-1-methylethyl)-2,4,6(1H,3H,5H)-pyrimidinetrione (CASRN 223717-84-8) represented by the Formula IR-1:
The infrared dye IR-1 has an absorption maximum λmax of 1052 nm making it very suitable for a Nd-YAG laser having an emission wavelength of 1064 nm.
Infrared dyes having an absorption maximum between 830 nm and 1000 nm are preferably selected from the group consisting of quinoline dyes, indolenine dyes, especially benzo[e]indolenine dyes, and benzo[f]indolenine dyes.
The amount of the IR dyes is preferably between 0.005 and 1.000 g/m2, more preferably between 0.010 and 0.500 g/m2, most preferably between 0.015 and 0.050 g/m2. Enough IR dye has to be present to ensure sufficient colour density formation upon exposure to IR radiation. However, using too much IR dye may result in unwanted background colouration of the laser markable materials.
Inorganic infrared absorbing pigments, such as carbon black, may be used in combination with the infrared dyes, such as disclosed in the unpublished EP-A 14172285.0 (filed on Jun. 13, 2014).
In another embodiment of the invention, a first and a second laser markable layer of the colour laser markable article comprise respectively an infrared absorbing dye and an infrared absorbing pigment.
The first and the second laser markable layer may be individually addressed by lasers having a different operation mode. For example when an infrared absorbing pigment is used in the first laser markable layer and an infrared dye in the second laser markable layer, the layer containing the pigment may be addressed by a laser working in a pulsed mode while the layer containing the infrared dye may be addressed by a laser working in a continuous mode.
Suitable examples of infrared absorbing pigments include but are not limited to carbon black such as acetylene black, channel black, furnace black, lamp black, and thermal black; oxides, hydroxides, sulfides, sulfates and phosphates of metals such as copper, bismuth, iron, nickel, tin, zinc, manganese, zirconium, tungsten, lanthanum, and antimony including lanthane hexaboride, indium tin oxide (ITO) and antimony tin oxide, titanium black and black iron oxide.
The infrared dye classes disclosed above may also be used as infrared absorbing pigments, for example cyanine pigment, merocyanine pigment, etc.
A preferred infrared absorbing pigment is carbon black.
The particle size of the pigment is preferably from 0.01 to 5 μm, more preferably from 0.05 to 1 μm.
The amount of the infrared absorbing pigment is between 10 and 1000 ppm, preferably between 25 and 750 ppm, more preferably between 50 and 500 ppm, most preferably between 100 and 250 ppm, all relative to the total dry weight of the laser markable layer. An amount of infrared absorbing pigment above 1000 ppm results in a too high background density of the laser markable article.
All publicly-known leuco dyes can be used and are not restricted. They are for example widely used in conventional pressure-sensitive, photosensitive or thermally-sensitive recording materials. For more information about leuco dyes, see for example Chemistry and Applications of Leuco Dyes, Ramaiah Muthyala, Plenum Press, 1997.
A number of classes of leuco dyes may be used as colour forming compounds in the present invention, such as for example: spiropyran leuco dyes such as spirobenzopyrans (e.g. spiroindolinobenzopyrans, spirobenzo-pyranobenzopyrans, 2,2-dialkylchromenes), spironaphtooxazine and spirothiopyran; leuco quinone dyes; azines such as oxazines, diazines, thiazines and phenazine; phthalide- and phthalimidine-type leuco dyes such as triarylmethane phtalides (e.g. crystal violet lactone), diarylmethane phthalides, monoarylmethane phthalides, heterocyclic substituted phthalides, alkenyl substituted phthalides, bridged phthalides (e.g. spirofluorene phthalides and spirobenzanthracene phthalides) and bisphthalides; fluoran leuco dyes such as fluoresceins, rhodamines and rhodols; triarylmethanes such as leuco crystal violet; ketazines; barbituric acid leuco dyes and thiobarbituric acid leuco dyes.
The laser markable layer(s) may comprise more then one leuco dye, typically to obtain a specific desired colour.
The leuco dye is preferably present in the laser markable layer in an amount of 0.05 to 5.00 g/m2, more preferably in an amount of 0.10 to 3.00 g/m2, most preferably in an amount of 0.20 to 1.00 g/m2.
The following reaction mechanisms and leuco dyes are suitable to form a coloured dye.
The reaction mechanism can be represented by:
Leuco-dye+acid generator→Leuco-dye+acid→Coloured Dye
All publicly-known photo- and thermal acid generators can be used for the present invention. They can optionally be combined with a photosensitizing dye. Photo- and thermal acid generators are for example widely used in conventional photoresist material. For more information see for example “Encyclopaedia of polymer science”, 4th edition, Wiley or “Industrial Photoinitiators, A Technical Guide”, CRC Press 2010.
Preferred classes of photo- and thermal acid generators are iodonium salts, sulfonium salts, ferrocenium salts, sulfonyl oximes, halomethyl triazines, halomethylarylsulfone, α-haloacetophenones, sulfonate esters, t-butyl esters, allyl substituted phenols, t-butyl carbonates, sulfate esters, phosphate esters and phosphonate esters.
Preferred Leuco Dyes are phthalide- and phthalimidine-type leuco dyes such as triarylmethane phtalides, diarylmethane phthalides, monoarylmethane phthalides, heterocyclic substituted phthalides, alkenyl substituted phthalides, bridged phthalides (e.g. spirofluorene phthalides and spirobenzanthracene phthalides) and bisphthalides; and fluoran Leuco Dyes such as fluoresceins, rhodamines and rhodols.
In a more preferred embodiment of the present invention, a combination is used of at least one compound selected from the group consisting of CASRN 50292-95-0, CASRN 89331-94-2, CASRN1552-42-7 (crystal violet lactone), CASRN148716-90-9, CASRN 630-88-6, CASRN 36889-76-7 or CASRN 132467-74-4 as the Leuco Dye and at least one compound selected from the group consisting of CASRN 58109-40-3, CASRN 300374-81-6, CASRN 1224635-68-0, CASRN 949-42-8, CASRN 69432-40-2, CASRN 3584-23-4, CASRN 74227-35-3, CASRN 953-91-3 or CASRN6542-67-2 as acid generator.
The reaction mechanism can be represented by:
wherein R1, R2 and R3 each independently represent an amino group, an optionally substituted mono- or dialkylamino group, a hydroxyl group or an alkoxy group. R1 and R3 also each independently represent a hydrogen atom or an optionally substituted alkyl, aryl, or heteroaryl group. A preferred leuco dye for the present invention is leuco crystal violet (CASRN 603-48-5).
The reaction mechanism can be represented by
wherein X represents an oxygen atom or an optionally substituted amino or methine group.
The reaction mechanism can be represented by:
Leuco Dye−FG→Dye
wherein FG represents a fragmenting group.
Preferred leuco dyes are oxazines, diazines, thiazines and phenazine. A particularly preferred leuco dye (CASRN104434-37-9) is shown in EP 174054 (POLAROID) which discloses a thermal imaging method for forming colour images by the irreversible unimolecular fragmentation of one or more thermally unstable carbamate moieties of an organic compound to give a visually discernible colour shift from colourless to coloured.
The fragmentation of a leuco dye may be catalyzed or amplified by acids, photo acid generators, and thermal acid generators.
The reaction mechanism can be represented by:
wherein X1 represents an oxygen atom, an amino group, a sulphur atom or a selenium atom and X2 represents an optionally substituted methine group or a nitrogen atom.
The preferred spiropyran leuco dyes for the present invention are spiro-benzopyrans such as spiroindolinobenzopyrans, spirobenzopyranobenzopyrans, 2,2-dialkylchromenes; spironaphtooxazines and spirothiopyrans. In a particularly preferred embodiment, the spiropyran leuco dyes are CASRN 160451-52-5 or CASRN 393803-36-6. The ring opening of a spiropyran leuco dye may be catalyzed or amplified by acids, photo acid generators, and thermal acid generators.
IR-leuco Dyes are leuco dyes which have a main absorption in the Infrared. Preferred IR-Leuco Dyes are disclosed in EP-A 1736312 and have a structure according to formula I
wherein at least one of the Rd groups is a group which is transformed by a chemical reaction, induced by exposure to IR radiation or heat, into a group which is a stronger electron-donor than said Rd; or wherein at least one of the Ra groups is a group which is transformed by a chemical reaction, induced by exposure to IR-radiation or heat, into a group which is a stronger electron acceptor than said Ra.
Even more preferred IR-Leuco Dyes are the N-meso substituted cyanine, merocyanine or oxonole dyes wherein the N-meso substituents comprises electron withdrawing groups, disclosed in EP-A 2234964. The most preferred IR-Leuco Dyes are cyanine dyes with —NCH3—CO—OC(CH3)3, —NCH3—SO2—CF3 or —NCH3—SO2—C6H4—CH3 meso substituted cyanine dyes. Specific structures of IR-Leuco Dyes are
The reaction mechanism, as described in US20070212643, can be represented by the transformation of an IR cyanine dye with partial structure represented by formula (3-1) into a coloured compound with a partial structure represented by formula (3-2):
wherein X represents a hydrogen atom, a halogen atom, a hydroxyl group, an amino group, a nitro group, a mercapto group, a sulfonic acid group a phosphoric acid group or a monovalent organic group. X preferably represents a diphenylamino group. A particularly preferred IR-Leuco Dye for the present invention has the following structure:
In a preferred embodiment of a laser markable layer for producing a cyan colour, the cyan colour forming compound has a structure according to Formulae CCFC1, CCFC2 or CCFC3.
In a preferred embodiment of a laser markable layer for producing a magenta colour, the magenta colour forming compound has a structure according to Formula MCFC2:
In a preferred embodiment of a laser markable layer for producing a red colour, the red colour forming compound has a structure according to Formula RCFC:
In a preferred embodiment of a laser markable layer for producing a yellow colour, the yellow colour forming compound has a structure according to Formula YCFC:
wherein R, R′ are independently selected from a group consisting of a linear alkyl group, a branched alkyl group, an aryl and aralkyl group.
In one embodiment, the yellow colour forming compound has a structure according to Formula YCFC, wherein R and R′ independently represent a linear alkyl group, a branched alkyl group, an aryl or an aralkyl group substituted by at least one functional group containing an oxygen atom, a sulphur atom or a nitrogen atom.
A particularly preferred yellow colour forming compound is the compound according to Formula YCFC wherein both R and R′ are methyl.
In a most preferred embodiment of a laser markable layer for producing a yellow colour, the yellow colour forming compound has a structure according to Formulae YCFC1 or YCFC2
In a preferred embodiment of a laser markable layer for producing a black colour, the black colour forming compound has a structure according to Formula BCFC
wherein Me=methyl and Et=Ethyl.
The laser markable layer may include a polymeric binder. In principle any suitable polymeric binder that does not prevent the colour formation in the laser markable layer(s) may be used. The polymeric binder may be a polymer, a copolymer or a combination thereof.
The laser markable layer preferably includes a water soluble or dispersible binder.
Examples of water soluble or dispersible binder are homopolymers and copolymers of vinyl alcohol, (meth)acrylamide, methylol (meth)acrylamide, (meth)acrylic acid, hydroxyethyl (meth) acrylate, maleic anhydride/vinylmethylether copolymers, copolymers of (meth)acrylic acid or vinylalcohol with styrene sulphonic acid, vinyl alcohol/vinylacetate copolymers, carboxy-modified polyvinyl alcohol, carboxymethyl cellulose, hydroxyethyl cellulose, cellulose sulfate, polyethylene oxides, gelatin, cationic starch, casein, sodium polyacrylate, styrene-maleic anhydride copolymer sodium salt, sodium polystyrene sulfonate.
Preferred vinyl alcohol-vinyl acetate copolymers are disclosed in EP-A 2103736, paragraph [79]-[82].
Other preferred water soluble or dispersible binders are the copolymers comprising alkylene and vinyl alcohol units disclosed in EP-A 2457737 paragraph [0013] to [0023] such as the Exceval™ type polymers from Kuraray.
The polymeric binder is preferably present in the colour forming layer in an amount of 1 to 30 g/m2, more preferably in an amount of 2 to 20 g/m2, most preferably in an amount of 3 to 10 g/m2.
The laser markable layer or another layer of the laser markable article may contain one or more acid scavengers.
Acid scavengers include organic or inorganic bases. Examples of the inorganic bases include hydroxides of alkali metals or alkaline earth metals; secondary or tertiary phosphates, borates, carbonates; quinolinates and metaborates of alkali metals or alkaline earth metals; a combination of zinc hydroxide or zinc oxide and a chelating agent (e.g., sodium picolinate); hydrotalcite such as Hycite 713 from Clariant; ammonium hydroxide; hydroxides of quaternary alkylammoniums; and hydroxides of other metals. Examples of the organic bases include aliphatic amines (e.g., trialkylamines, hydroxylamines and aliphatic polyamines); aromatic amines (e.g., N-alkyl-substituted aromatic amines, N-hydroxylalkyl-substituted aromatic amines and bis[p-(dialkylamino)phenyl]-methanes), heterocyclic amines, amidines, cyclic amidines, guanidines and cyclic guanidines.
Other preferred acid scavangers are HALS compounds. Example of suitable HALS include Tinuvin™ 292, Tinuvin™ 123, Tinuvin™ 1198, Tinuvin™ 1198 L, Tinuvin™ 144, Tinuvin™ 152, Tinuvin™ 292, Tinuvin™ 292 HP, Tinuvin™ 5100, Tinuvin™ 622 SF, Tinuvin™ 770 DF, Chimassorb™ 2020 FDL, Chimassorb™ 944 LD from BASF; Hostavin 3051, Hostavin 3050, Hostavin N 30, Hostavin N321, Hostavin N 845 PP, Hostavin PR 31 from Clariant.
Further examples of acid scavengers are salts of weak organic acids such as carboxylates (e.g. calcium stearate).
A preferred acid scavenger is an organic base, more preferably an amine.
A particular preferred acid scavenger is an organic base having a pKb of less than 7.
The laser markable article may also comprise an UV-absorber. The UV-absorber may be present in a laser markable layer or may also be present in another layer, for example an outer layer or an intermediate layer.
Examples of suitable UV-absorbers include 2-hydroxyphenyl-benzophenones (BP) such as Chimassorb™ 81 and Chimassorb™ 90 from BASF; 2-(2-hydroxyphenyl)-benzotriazoles (BTZ) such as Tinuvin™ 109, Tinuvin™ 1130, Tinuvin™ 171, Tinuvin™ 326, Tinuvin™ 328, Tinuvin™ 384-2, Tinuvin™ 99-2, Tinuvin™ 900, Tinuvin™ 928, Tinuvin™ Carboprotect™, Tinuvin™ 360, Tinuvin™ 1130, Tinuvin™ 327, Tinuvin™ 350, Tinuvin™ 234 from BASF, Mixxim™ BB/100 from FAIRMOUNT, Chiguard 5530 from Chitec; 2-hydroxy-phenyl-s-triazines (HPT) such as Tinuvin™ 460, Tinuvin™ 400, Tinuvin™ 405, Tinuvin™ 477, Tinuvin™ 479, Tinuvin™ 1577 ED, Tinuvin™ 1600 from BASF, 2-(2,4-dihydroxyphenyl)-4,6-bis-(2,4-dimethylphenyl)-s-triazine (CASRN1668-53-7) from Capot Chemical Ltd and 4-[4,6-bis(2-methyl-phenoxy)-1,3,5-triazin-2-yl]-1,3-benzenediol (CASRN13413-61-1); titanium dioxide such as Solasorb 100F from from Croda Chemicals; zink oxide such as Solasorb 200F from Croda Chemicals; benzoxazines such as Cyasorb UV-3638 F, CYASORB™ UV-1164 from CYTEC; and oxamides such as Sanduvor VSU from Clariant.
Preferred UV absorbers have in the wavelength region between 300 and 400 nm a maximum absorption above 330 nm, more preferably above 350 nm.
Particular preferred UV absorbers are hydroxyphenyl benzotriazoles and 2-hydroxyphenyl-s-triazines having a maximum absorption above 350 nm in the wavelength region 300-400 nm.
The colour laser markable material preferably includes a support, more preferably a transparent polymeric support, more preferably a transparent axially stretched polyester support. The laser markable layer is coated directly on the polymeric support or on a subbing layer present on the polymeric support for improving adhesion of the laser markable layer, thereby preventing falsification through delamination.
Suitable transparent polymeric supports include cellulose acetate propionate or cellulose acetate butyrate, polyesters such as polyethylene terephthalate and polyethylene naphthalate, polyamides, polycarbonates, polyimides, polyolefins, polyvinylchlorides, polyvinylacetals, polyethers and polysulphonamides.
In the most preferred embodiment, the transparent polymeric support is a biaxially stretched polyethylene terephthalate foil (PET-C foil) to be very durable and resistant to scratches and chemical substances.
The support preferably is a single component extrudate, but may also be a co-extrudate. Examples of suitable co-extrudates are PET/PETG and PET/PC.
Polyester supports and especially polyethylene terephthalate supports are preferred because of their excellent properties of dimensional stability. When polyester is used as the support material, a subbing layer is preferably employed to improve the bonding of layers, foils and/or laminates to the support.
The manufacturing of PET-C foils and supports is well-known in the art of preparing suitable supports for silver halide photographic films. For example, GB 811066 (ICI) teaches a process to produce biaxially oriented polyethylene terephthalate foils and supports.
The polyethylene terephthalate is preferably biaxially stretched with a stretching factor of at least 2.0, more preferably at least 3.0 and most preferably a stretching factor of about 3.5. The temperature used during stretching is preferably about 160° C.
Methods to obtain opaque polyethylene terephthalate and biaxially oriented films thereof of have been disclosed in, e.g. US2008/238086.
The polymeric support may be provided with one or more subbing layers. This has the advantage that the adhesion between the laser markable layer and the polymeric support is improved.
Useful subbing layers for this purpose are well known in the photographic art and include, for example, polymers of vinylidene chloride such as vinylidene chloride/acrylonitrile/acrylic acid terpolymers or vinylidene chloride/methyl acrylate/itaconic acid terpolymers.
Suitable vinylidene chloride copolymers include: the copolymer of vinylidene chloride, N-tert.-butylacrylamide, n-butyl acrylate, and N-vinyl pyrrolidone (e.g.70:23:3:4), the copolymer of vinylidene chloride, N-tert.-butylacrylamide, n-butyl acrylate, and itaconic acid (e.g. 70:21:5:2), the copolymer of vinylidene chloride, N-tert.-butylacrylamide, and itaconic acid (e.g. 88:10:2), the copolymer of vinylidene chloride, n-butylmaleimide, and itaconic acid (e.g. 90:8:2), the copolymer of vinyl chloride, vinylidene chloride, and methacrylic acid (e.g. 65:30:5), the copolymer of vinylidene chloride, vinyl chloride, and itaconic acid (e.g. 70:26:4), the copolymer of vinyl chloride, n-butyl acrylate, and itaconic acid (e.g. 66:30:4), the copolymer of vinylidene chloride, n-butyl acrylate, and itaconic acid (e.g. 80:18:2), the copolymer of vinylidene chloride, methyl acrylate, and itaconic acid (e.g.90:8:2), the copolymer of vinyl chloride, vinylidene chloride, N-tert.-butylacrylamide, and itaconic acid (e.g. 50:30:18:2). All the ratios given between brackets in the above-mentioned copolymers are ratios by weight.
In a preferred embodiment, the transparent oriented polyester support is provided with a subbing layer including a binder based on a polyester-urethane copolymer.
In a more preferred embodiment, the polyester-urethane copolymer is an ionomer type polyester urethane, preferably using polyester segments based on terephthalic acid and ethylene glycol and hexamethylene diisocyanate.
A suitable polyester-urethane copolymer is Hydran™ APX101 H from DIC Europe GmbH.
The application of subbing layers is well-known in the art of manufacturing polyester supports for silver halide photographic films. For example, the preparation of such subbing layers is disclosed in U.S. Pat. No. 3,649,336 (AGFA) and GB 1441591 (AG FA);
In a preferred embodiment, the subbing layer has a dry thickness of no more than 0.2 μm or preferably no more than 200 mg/m2.
The laser markable material may in addition to the laser markable layer or layers contain additional layers, such as for example subbing layers, an outer layer that is suitable as a receiver layer for dyes applied by thermal dye sublimation or even inkjet printing, or intermediate layers between the laser markable layer and the support to improve the adhesion.
The laser markable material preferably comprises an intermediate layer between the laser markable layers to prevent colour contamination. Such an intermediate layer may be a polymeric film such as disclosed in EP-A 2719541 but is preferably a coated layer, preferably a layer coated from an aqueous coating solution.
These intermediate layers preferably contain an acid scavenger as disclosed above to prevent diffusion of an acid from one laser markable layer to another.
The intermediate layers preferably also contain an UV absorber as disclosed above to improve the daylight stability of the laser markable materials.
A preferred embodiment of a laser markable material according to the present invention is shown in
Another preferred embodiment of a laser markable material, a security document precursor, is shown in
The colour laser markable document precursor or document may include a core support. The core support may be transparent or opaque. The core support is preferably an opaque white core support. The advantage of an opaque white core support is that any information present on the document is more easily readable and that a colour image is more appealing by having a white background.
Preferred opaque white core supports include resin coated paper supports, such as polyethylene coated paper and polypropylene coated paper, and synthetic paper supports such as Synaps™ synthetic paper of Agfa-Gevaert NV.
Other examples of useful high-quality polymeric supports for the present invention include opaque white polyesters and extrusion blends of polyethylene terephthalate and polypropylene. Also Teslin™ may be used as support.
Instead of a white support, a white opacifying layer can be coated onto a transparent polymeric support, such as those disclosed above. The opacifying layer preferably contains a white pigment with a refractive index greater than 1.60, preferably greater than 2.00, and most preferably greater than 2.60. The white pigments may be employed singly or in combination. Suitable white pigments include C. I. Pigment White 1, 3, 4, 5, 6, 7, 10, 11, 12, 14, 17, 18, 19, 21, 24, 25, 27, 28 and 32. Preferably titanium dioxide is used as pigment with a refractive index greater than 1.60. Titanium oxide occurs in the crystalline forms of anatase type, rutile type and brookite type. In the present invention the rutile type is preferred because it has a very high refractive index, exhibiting a high covering power.
A method for preparing a laser marked article according to a preferred embodiment of the present invention uses at least two infrared lasers L-1 and L-2 having respectively a laser emission wavelength of λ(L-1) and λ(L-2) comprising the steps of:
A particluar preferred method for preparing a laser marked article uses three infrared lasers L-1, L-2 and L-3 having respectively a laser emission wavelength of λ(L-1), λ(L-2) and λ(L-3) comprising the step:
In a preferred embodiment, the emission wavelengths of the infrared lasers L-1, L-2 and L-3 are selected to fulfill the following conditions: a) λ(L-1)>1100 nm; b) 1000 nm<λ(L-2)<1100 nm; and c) λ(L-3)<1000 nm.
In a very preferred embodiment, the emission wavelength of the infrared laser L-1 is between 1125 nm and 1200 nm.
Colour fogging is minimized by using the lasers in a wavelength range near the absorption maximum of the corresponding infrared dye. Preferably the laser emission wavelengths λ(L-1), λ(L-2) and λ(L-3) differ by no more than 30 nm from the infrared red dye absorption maxima λmax(IR-1), λmax(IR-2) and respectively λmax(IR-3).
The methods described above may be used to laser mark any surface or support which is provided with the laser markable layers described above.
In a preferred embodiment, the laser marked article is a security document selected from the group consisting of a passport, a personal identification card and a product identification document.
The laser markable article is preferably combined with one or more other security features to increase the difficulty for falsifying the document.
To prevent forgeries of identification documents, different means of securing are used. One solution consists in superimposing lines or guilloches on an identification picture such as a photograph. In that way, if any material is printed subsequently, the guilloches appear in white on added black background. Other solutions consist in adding security elements such as information printed with ink that reacts to ultraviolet radiation, micro-letters concealed in an image or text etc.
Suitable other security features such as anti-copy patterns, guilloches, endless text, miniprint, microprint, nanoprint, rainbow colouring, 1D-barcode, 2D-barcode, coloured fibres, fluorescent fibres and planchettes, fluorescent pigments, OVD and DOVID (such as holograms, 2D and 3D holograms, kinegrams™, overprint, relief embossing, perforations, metallic pigments, magnetic material, Metamora colours, microchips, RFID chips, images made with OVI (Optically Variable Ink) such as iridescent and photochromic ink, images made with thermochromic ink, phosphorescent pigments and dyes, watermarks including duotone and multitone watermarks, ghost images and security threads.
All materials used in the following examples were readily available from standard sources such as ALDRICH CHEMICAL Co. (Belgium) and ACROS (Belgium) unless otherwise specified. The water used was deionized water.
Takenate D11ON is a aliphatic polyisocyanate adduct prepolymer commercially available from Mitsui.
Mowiol 4 88 is a polyvinyl alcohol commercially available from Hoechst.
Olfine E1010 is a wetting agent commercially available from Shin-Etsu Chemical Company.
Arlo is a 15 wt % aqueous solution of Marlon A365, commercially available from Brenntag.
Proxel Ultra 5 is a biocide, commercially available from Avecia.
Ralox 46 is a sterically hindered phenolix antioxidant from Raschig.
Tinuvin 928 is an UV absorber commercially available from BASF.
DISFLAMOLL TKP is a low volatility halogen free phosphate plasticer from Lanxess.
Proxelk is an 5 wt % aqueous solution of 1,2-benzisothiazoline-3-one potassium salt (CASRN 127553-58-6, commercially available from Prom Chem).
MOW is an aqueous solution of bearing 15 wt % Mowiol 4 88 and 2 wt % Proxelk.
CCE is Bayhydrol H 2558, an anionic polyester urethane (37.3%) from BAYER.
Resorcinol is commercially available from Sumitomo Chemicals.
Par is a dimethyltrimethylolamine formaldehyde resin from Cytec industries.
PAR-sol is a 40 wt % aqueous solution of Par.
PEA is Tospearl™ 120 from Momentive Performance materials.
PEA-sol is a 10 wt % (50/50) aqueous/ethanol dispersion of PEA.
Dowfax™ 2A1 from Pilot Chemicals C is a Alkyldiphenyloxide disulfonate (4.5% wt).
MEK is an abbreviation used for methylethylketone.
Solvin™ 557RB is a vinylchloride-vinylacetate copolymer with 11% vinyl acetate, provided by SOLVAY.
SolvinSol is a 12.5 wt % solution of Solvin™ 557RB in MEK.
Vinnol™ H40/55 is a copolymer of 62 wt % vinyl chloride and 38 wt % of vinyl acetate provided by Wacker AG.
VinnolSol is a 12.5 wt % solution of Vinnol™ H40/55 in MEK.
HDP is the hydrogen donor-precursor CASRN 129104-70-7 prepared according to the synthesis given on page 31 of EP 605149 A (JUJO PAPER) for the compound (19).
DOW-sol is a 2.5wt % solution of Dowfax™ 2A1 in isopropanol.
Surfynol™ 420 from Air Products is a non ionic surfactant.
Surfynsol is a 2.5wt % solution of Surfynol™ 420 in isopropanol.
CORE is a 500 μm opaque PETG core available as PET-G 500 type 9311 from WOLFEN.
920IRsol is a 0.15 wt % solution in MEK of the infrared dye 920IR.
1064IRsol is a 0.15 wt % solution in MEK of the infrared dye 1064IR.
1150IR2sol is a 0.15 wt % solution in MEK of the infrared dye 1150IR2.
YLD1 is a leuco dye prepared as follows:
55 g fluorescein, disodium salt (Acros Chemicals) and 55 g potassium hydroxide were dissolved in 110 ml water. 150 g 1-bromohexane (Sigma-Aldrich) and 3 g tetrabutylammonium bromide (Merck) were added to the solution. The reaction mixture was stirred under reflux during 24 h. 200 g toluene and 80 g water were added to the reaction mixture which was further stirred under reflux for 30 minutes. The organic phase was dried with sodium sulphate and evaporated under reduced pressure. The desired product was recrystallised from isopropanol. The compound was analyzed using TLC-chromatography (TLC Silica gel 60 Partisil KC18F; supplied by Whatman, eluent: methanol, Rf: 0.4).
YLD2 is a leuco dye with the following formula commercially available from TCI.
BLD1 is a leuco dye with the following formula commercially available from Mitsui.
BLD2 is a leuco dye with the following formula commercially available from Mitsui.
BLD3 is a leuco dye with the following formula commercially available from Yamada Chemical Co.
MLD1 is a leuco dye with the following formula commercially available from Mitsui.
MLD2 is a leuco dye with the following formula commercially available from Connect Chemical.
MLD3is a leuco dye with the following formula commercially available from BASF
1150IR1 is an IR dye prepared as follows:
The synthesis of intermediate INT-2 was performed as disclosed in [0157] of EP 2463109 A (AGFA). The synthesis of intermediate INT-1 was performed as follows. 10 mol of dimethylformamide and 3 mol phosphoryl chloride were heated up to 65° C. Then 1 mol of cyclopentanon was dropped to this mixture. After one hour of stirring at 60° C., the reaction mixture was poured into 2 1 water containing 7 mol sodium acetate. INT-1 was filtered and dried. The yield was 60%. The compound was analyzed using TLC-chromatography (TLC Silica gel 60 F254; supplied by Merck, eluent: methylene chloride/methanol 90/10, Rf: 0.75).
To a stirred mixture of INT-1 containing 23% water (10.3 g; 0.05 mol) and INT-2 (36.5 g; 0.1 mol) in methanol (250 mL) was added a mixture of acetic acid (10.1 g; 0.1 mol) and triethylamine (18 g; 0.3 mol) over a 1 hour period. Stirring (under nitrogen) was continued for 1 hour at room temperature. The black precipitate was filtered and digested consecutively with 2×20 mL of methanol and 2×50 mL of methyl tertiary butylether (MTBE) and dried in vacuum. Yield of INT-3 (black powder): 27 g (74.6%). The compound was analyzed using TLC-chromatography (TLC Silica gel 60 F254; supplied by Merck, eluent: methanol/acetone 75/25, Rf: 0.4).
To a stirred suspension of INT-3 (500 mg; 0.69 mmol) in a mixture of ethanol (9 mL) and water (1 mL) at room temperature was added sodium benzenesulfonate (CASRN873-55-2; 135 mg; 0.82 mmol). After stirring for 15 minutes, the black precipitate was filtered, digested with a mixture of ethanol (4.5 mL) and water (0.5 mL) and dried in vacuo. The yield of 1150IR1 (black powder) was 467 mg (81%).
The absorption maximum measured in methanol was 1104 nm. The absorption maximum of 1150IR1 measured in CH2Cl2 including 6.5×10−6 wt % of methanesulfonic acid was 1120 nm using a SHIMADZU UV-2101 PC spectrophotometer.
1150IR2 is an IR dye prepared as follows:
The synthesis of intermediate INT-1 was performed as follows. 10 mol of dimethylformamide and 3 mol phosphoryl chloride were heated up to 65° C. Then 1 mol of cyclopentanon was dropped to this mixture. After one hour of stirring at 60° C., the reaction mixture was poured into 2 1 water containing 7 mol sodium acetate. INT-1 was filtered and dried. The yield was 60%. The compound was analyzed using TLC-chromatography (TLC Silica gel 60 F254; supplied by Merck, eluent: methylene chloride/methanol 90/10, Rf: 0.75).
INT-7 was purchased from Spectrum Info ltd. And can be synthesized according to Ukrainskii khimicheskii zhurnal, 74, p105-113, 2008 and the references their in (Ukrainskii khimicheskii zhurnal, 73, p 120-125, 2007 and U.S. Pat. No. 2,108,879).
To a stirred mixture of 3.83 g INT-7 and 0.86 g INT-1 in methanol (25 ml) at room temperature under nitrogen were added consecutively triethylamine (1 g) and acetic acid (1.8 g). The reaction was stirred for 4 hours at room temperature. The product was isolated by filtration, washed with methanol and methyl t-butyl ether. The product was dried at room temperature under reduced pressure and stored at 4° C.). The compound was analyzed using TLC-chromatography (TLC Silica gel 60 F254; supplied by Merck, eluent: methylene chloride/methanol 90/10, Rf: 0.35).
To a stirred suspension of INT-8 (1.6 g) in acetone (15 ml), 0.49 g sodium benzenesulfinate (CASRN873-55-2) and 0.64 g tetrabutyl ammonium bromide was added at room temperature. The suspension was stirred for 1 hour. The product was isolated by filtration and washed with acetone, water and methyl t-butyl ether. The product was dried at room temperature under reduced pressure and stored at 4° C.). The compound was analyzed using TLC-chromatography (TLC Silica gel 60 F254; supplied by Merck, eluent: methylene chloride/methanol 90/10, Rf: 0.4).
1064IR is an IR dye with the following formula and synthesized as disclosed in paragraphs [0150] to [0159] of EP-A 2463109.
920IR is an IR dye prepared as follows:
The intermediate INT-1 was prepared in the same manner as described here above. The synthesis of the intermediate INT-4 was performed as described by paragraphs [0097] and [0098] of US20040182268 A1 (AGFA). To a stirred mixture of INT-1 (4.75 g; 30 mmol) and INT-4 (20.8 g; 60 mmol) in ethanol (100 mL) at room temperature were added consecutively triethylamine (12.1 g; 120 mmol) and acetic acid anhydride (12.2 g; 120 mmol). After heating to 50° C. for 1 hour, the reaction mixture was cooled to 20° C. and isopropanol (100 mL) was added. After 1 hour the precipitated IR-absorber was isolated by filtration, washed with EtOAc (20 mL) and dried in vacuo. Yield (crude) of INT-5 was 16 g (73%).
The absorption maximum of INT-5 measured in methanol was 844 nm using a SHIMADZU UV-2101 PC spectrophotometer.
To a stirred suspension of INT-5 (16 g; 22 mmol) in acetonitrile (200 mL) was added potassium nonafluorobutanesulfonate (CASRN29420-49-3 from TCI Europe N. V.; 8.1 g; 24 mmol) and this mixture was heated at 70° C. for 15 minutes. After cooling to room temperature, water (100 mL) was drop wise added and after stirring for 2 hours the precipitated IR-absorber was isolated by filtration, washed consecutively with a mixture of acetonitrile/water 2/1 (20 mL), methyl t-butyl ether (20 mL) and dried in vacuum. The yield of INT-6 was 14 g (67%). The absorption maximum of INT-8 measured in methanol was 844 nm using a SHIMADZU UV-2101 PC spectrophotometer.
To a stirred suspension of INT-6 (1.65 g; 1.73 mmol) in methanol (15 mL) under nitrogen at room temperature is added sodium benzenesulfinate (CASRN873-55-2 from Aldrich; 0.297 g; 1.81 mmol). After stirring for 2 hours the precipitated IR-absorber was isolated by filtration, washed with MTBE (5 mL) and dried in vacuum. The yield of 920IR was 1.2 g (65%). The absorption maximum measured in methanol was 910 nm. The absorption maximum of IR-3 measured in CH2Cl2 including 6.5×10−6 wt % of methanesulfonic acid was 923 nm using a SHIMADZU UV-2101 PC spectrophotometer.
YDISP is a dispersion prepared as follows:
10 g YLD1 was added to 32 g ethyl acetate. 30.8 g Takenate D110N was added to the mixture. The mixture was stirred at 70° C. during 10 minutes in order to dissolve the components. The mixture was brought at 25° C. 0.15 g 1150IR1 dissolved in 3 ml methylene chloride was added to the mixture.
In a separate flask, 0.06 g Olfine E1010 was added to 77 g of a 12 wt % solution of Mowiol 4 88 in water.
The ethyl acetate-based solution was added to the aqueous solution. The mixture was emulsified using a T25 digital Ultra-turrax® with a 18N rotor commercially available from IKA at 19000 rpm during 5 minutes. The emulsion was stirred at 25° C. and 76.39 g water was added.
Ethyl acetate was removed under reduced pressure by following procedure: successively 5 minutes at 150 mbar at room temperature, 10 minutes at 120 mbar and 50° C. and 10 minutes at 100 mbar and 50° C. The mixture was brought at room temperature and 20 ml water was added. The mixture was stirred during 1 hour at 60° C. and 20 hours at 45° C. Large particles were removed by filtering the mixture using a cloth filter with 30 μm pores.
BDISP is a dispersion prepared as follows:
6 g BLD1 and 4 g BLD2 was added to 32 g ethyl acetate. 30.8 g Takenate D110N was added to the mixture. The mixture was stirred at 70° C. during 10 minutes in order to dissolve the components. The mixture was brought at 25° C. 0.1 g 1064IR dissolved in 3 ml methylene chloride was added to the mixture.
In a separate flask, 0.06 g Olfine E1010 was added to 77 g of a 12 wt % solution of Mowiol 4 88 in water.
The ethyl acetate-based solution was added to the aqueous solution. The mixture was emulsified using a T25 digital Ultra-turrax® with a 18N rotor commercially available from IKA at 19000 rpm during 5 minutes. The emulsion was stirred at 25° C. and 76.44 g water was added.
Ethyl acetate was removed under reduced pressure by following procedure: successively 5 minutes at 150 mbar at room temperature, 10 minutes at 120 mbar and 50° C. and 10 minutes at 100 mbar and 50° C. The mixture was brought at room temperature and 20 ml water was added. The mixture was stirred during 1 hour at 60° C. and 20 hours at 45° C. Large particles were removed by filtering the mixture using a cloth filter with 30 μm pores.
MDISP is a dispersion prepared as follows:
6 g MLD1 and 4 g MLD2 was added to 32 g ethyl acetate. 30.8 g Takenate D110N was added to the mixture. The mixture was stirred at 70° C. during 10 minutes in order to dissolve the components. The mixture was brought at 25° C. 0.2 g 920IR dissolved in 3 ml methylene chloride was added to the mixture.
In a separate flask, 0.06 g Olfine E1010 was added to 77 g of a 12 wt % solution of Mowiol 4 88 in water.
The ethyl acetate-based solution was added to the aqueous solution. The mixture was emulsified using a T25 digital Ultra-turrax® with a 18N rotor commercially available from IKA at 19000 rpm during 5 minutes. The emulsion was stirred at 25° C. and 76.34 g water was added.
Ethyl acetate was removed under reduced pressure by following procedure: successively 5 minutes at 150 mbar at room temperature, 10 minutes at 120 mbar and 50° C. and 10 minutes at 100 mbar and 50° C. The mixture was brought at room temperature and 20 ml water was added. The mixture was stirred during 1 hour at 60° C. and 20 hours at 45° C. Large particles were removed by filtering the mixture using a cloth filter with 30 μm pores.
DEVELOP is a dispersion prepared as follows:
In Pot A, 55 g of Arlo, 4.4 g Proxel Ultra 5 (commercially available from Avecia) and 366.674 MOW were added to 524.601 g water. The mixture was stirred for 5 minutes at 50° C. in order to dissolve all components.
In Pot B, 10.725 g 4,4′-Thiobis(6-tert-butyl-m-cresol) (commercially available from TCI Europe), 10.725 g Ralox 46 (commercially available from Raschig), 33 g Tinuvin 928 (commercially available from BASF), 8.25 g DISFLAMOLL TKP (commercially available from Lanxess), 4.125 g Ethyl Maleate (commercially available from TCI Europe) and 181.5 g Zinc 3,5-bis(alpha methylbenzyl) salicylate (CASRN53770-52-8, commercially available from Sanko Europe) were added to 495 g Ethyl acetate. The mixture was stirred for 30 minutes at 50° C. in order to dissolve all components.
While Pot A was stirred with a HOMO-REX high speed homogenizing mixer the solution in Pot B was added to Pot A. The mixture was further stirred during 5 minutes with the HOMO-REX mixer. Ethyl acetate was removed from the mixture under reduced pressure.
A coating composition SUB-1 was prepared by mixing the components according to Table 2 using a dissolver.
A 1100 μm thick polyethylene terephthalate sheet was first longitudinally stretched and then coated on both sides with the coating composition SUB-1 at a wet coating thickness of 10 μm. After drying, the longitudinally stretched and coated polyethylene terephthalate sheet was transversally stretched to produce a double side subbed 63 μm thick sheet PET-C, which was transparent and glossy.
15 ml DEVELOP was added to 10 ml YDISP. The mixture was stirred during 5 minutes at room temperature with a magnetic stirrer. The mixture was coated with an Elcometer Bird Film Applicator (from ELCOMETER INSTRUMENTS) on a PET-C support at a wet coating thickness of 60 μm and dried at 50° C. for 10 minutes in a circulation oven.
15 ml DEVELOP was added to 10 ml MDISP. The mixture was stirred during 5 minutes at room temperature with a magnetic stirrer. The mixture was coated with an Elcometer Bird Film Applicator (from ELCOMETER INSTRUMENTS) on a PET-C support at a wet coating thickness of 60 μm and dried at 50° C. for 10 minutes in a circulation oven.
15 ml DEVELOP was added to 10 ml BDISP. The mixture was stirred during 5 minutes at room temperature with a magnetic stirrer. The mixture was coated with an Elcometer Bird Film Applicator (from ELCOMETER INSTRUMENTS) on a PET-C support at a wet coating thickness of 60 μm and dried at 50° C. for 10 minutes in a circulation oven.
An assembly was made of, in order, a white opaque core support CORE, the laser markable inner laminate YL, the laser markable laminate BL and the laser markable laminate ML, wherein the side coated of the Laser Markable Laminate YL, BL and ML faces the white opaque core support CORE.
The lamination was performed using a Photonex-325 LSI laminator at a temperature of 120° C. and speed mode 5.
The laser markable article LMA was then laser marked with three infrared lasers of different emission wavelength. The optical density was measured in reflection using a spectrodensitometer Type GretagMacbeth SPM50 using a visual filter.
A first optically pumped semiconductor laser emitting at 920 nm (Genesis MX 920-4000 MTM from COHERENT) was used for producing a magenta coloured wedge of 0.6 cm×0.6 cm square boxes of increasing optical density up to a maximum optical density of 2.99 in the laser markable layer coated from ML. The laser was used at a power level of 1.92 W, a dither of 0.025, a scan speed of 100 mm/s and at a pulse repetition rate of 1.2 kHz.
A second optically pumped semiconductor laser emitting at 1064 nm (Genesis MX 1064-10000 MTM from COHERENT) was used for producing a blue coloured wedge of 0.6 cm×0.6 cm square boxes of increasing optical density up to a maximum optical density of 1.84 in the laser markable layer coated from BL. The laser was used at a power level of 2.43 W (21.8 A), a dither of 0.025, a scan speed of 100 mm/s and at a pulse repetition rate of 1.2 kHz.
A third optically pumped semiconductor laser emitting at 1154 nm (Genesis MX 1154-6000 MTM from COHERENT) was used for producing a yellow coloured wedge of 0.6 cm×0.6 cm square boxes of increasing optical density up to a maximum optical density of 1.23 in the laser markable layer coated from YL. The laser was used at a power level of 4.1 W, a dither of 0.025, a scan speed of 100 mm/s and at a pulse repetition rate of 1.2 kHz.
No colour contamination was observed in the different coloured wedges. This means that none of the three lasers caused any colour formation in a laser markable layer other than the one for which it was intended. For example, the 920 nm laser caused no blue respectively yellow colour formation in the laser markable layers coated from BL and YL.
The light stability was evaluated by measuring the OD of the security documents after exposing them to a suntest using an Atlas™ Suntest with a xenon-lamp for 5 hours at 765 W/m2. The optical density was measured in reflection using a spectrodensitometer Type GretagMacbeth SPM50 using a visual filter. The OD before the suntest was 0.37, after the suntest 0.40. In other words, the suntest resulted in an OD increase of 0.03.
The coating compositions BCOL and YCOL were prepared by mixing the components according to Table 3 using a dissolver.
The coating composition BCOL was coated with an Elcometer Bird Film Applicator (from ELCOMETER INSTRUMENTS) on one side of the PET-C support at a coating thickness of 100 μm and subsequently dried for 2 minutes at 20° C. on the film applicator and for a further 15 minutes in an oven at 75° C.
Then the coating composition YCOL was coated with an Elcometer Bird Film Applicator (from ELCOMETER INSTRUMENTS) on the opposite side of the PET-C support coated with BCOL at a coating thickness of 100 μm and subsequently dried for 2 minutes at 20° C. on the film applicator and for a further 15 minutes in an oven at 75° C. to deliver the laser markable inner laminate IL.
The coating composition MCOL was prepared by mixing the components according to Table 4 using a dissolver.
The coating composition MCOL was coated with an Elcometer Bird Film Applicator (from ELCOMETER INSTRUMENTS) on the subbed side of the PET-C support at a coating thickness of 100 μm and subsequently dried for 2 minutes at 20° C. on the film applicator and for a further 15 minutes in an oven at 75° C. to deliver the laser markable outer laminate OL.
An assembly was made of, in order, a white opaque core support CORE, the laser markable inner laminate IL, and the laser markable outer laminate OL, wherein the side coated with YCOL of the laser markable inner laminate IL and the side coated with MCOL of the laser markable outer laminate OL faces the white opaque core support.
The assembly was then laminated into a laser markable article LMA-02 using an Oasys™ OLA6/7 plate laminator with the settings: LPT=130° C., LP=40, Hold=210 sec, HPT=130° C. , HP=40 and ECT=50° C.
The laser markable article LMA-02 was then laser marked with three infrared lasers of different emission wavelength, as described above for LMA-01. The optical density was measured in reflection using a spectrodensitometer Type GretagMacbeth SPM50 using a visual filter.
No colour contamination was observed in the different coloured wedges. This means that none of the three lasers caused any colour formation in a laser markable layer other than the one for which it was intended. For example, the 920 nm laser caused no blue respectively yellow colour formation in the laser markable layers coated from BCOL and YCOL.
The light stability was evaluated by measuring the OD of the security documents after exposing them to a suntest using an Atlas™ Suntest with a xenon-lamp for 5 hours at 765 W/m2. The optical density was measured in reflection using a spectrodensitometer Type GretagMacbeth SPM50 using a visual filter. The OD before the suntest was 0.44, after the suntest 1.58. In other words, the suntest resulted in an OD increase of 1.14.
When comparing the suntest results of LMA-01, the inventive 3-colour Capsule Laser Markable Article, and those of LMA-02, the comparative 3-colour Non-Capsule Laser Markable Article, it is clear that the daylight stability of LMA-01 is much better the one of LMA-02.
Another advantage of the LMA-01, wherein the leuco dyes and the infrared dyes are encapsulated, is the fact that all laser markable layers were coated from aqueous coating solutions.
This application is a 371 National Stage Application of PCT/EP2015/060996, filed May 19, 2015, which is incorporated by reference herein in its entirety.
| Filing Document | Filing Date | Country | Kind |
|---|---|---|---|
| PCT/EP2015/060996 | 5/19/2015 | WO | 00 |
