EP0816116A1 - Compositions pour l'impression par transfert thermique - Google Patents

Compositions pour l'impression par transfert thermique Download PDF

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Publication number
EP0816116A1
EP0816116A1 EP97304195A EP97304195A EP0816116A1 EP 0816116 A1 EP0816116 A1 EP 0816116A1 EP 97304195 A EP97304195 A EP 97304195A EP 97304195 A EP97304195 A EP 97304195A EP 0816116 A1 EP0816116 A1 EP 0816116A1
Authority
EP
European Patent Office
Prior art keywords
thermal transfer
photochromic
coating formulation
compounds
derivatives
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Withdrawn
Application number
EP97304195A
Other languages
German (de)
English (en)
Inventor
Joseph D. Roth
Maurice W. Lewis
Yaoping Tan
John C. Rosenbaum
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
NCR International Inc
Original Assignee
NCR International Inc
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by NCR International Inc filed Critical NCR International Inc
Publication of EP0816116A1 publication Critical patent/EP0816116A1/fr
Withdrawn legal-status Critical Current

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Classifications

    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B41—PRINTING; LINING MACHINES; TYPEWRITERS; STAMPS
    • B41M—PRINTING, DUPLICATING, MARKING, OR COPYING PROCESSES; COLOUR PRINTING
    • B41M5/00—Duplicating or marking methods; Sheet materials for use therein
    • B41M5/26—Thermography ; Marking by high energetic means, e.g. laser otherwise than by burning, and characterised by the material used
    • B41M5/40—Thermography ; Marking by high energetic means, e.g. laser otherwise than by burning, and characterised by the material used characterised by the base backcoat, intermediate, or covering layers, e.g. for thermal transfer dye-donor or dye-receiver sheets; Heat, radiation filtering or absorbing means or layers; combined with other image registration layers or compositions; Special originals for reproduction by thermography
    • B41M5/46—Thermography ; Marking by high energetic means, e.g. laser otherwise than by burning, and characterised by the material used characterised by the base backcoat, intermediate, or covering layers, e.g. for thermal transfer dye-donor or dye-receiver sheets; Heat, radiation filtering or absorbing means or layers; combined with other image registration layers or compositions; Special originals for reproduction by thermography characterised by the light-to-heat converting means; characterised by the heat or radiation filtering or absorbing means or layers
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B41—PRINTING; LINING MACHINES; TYPEWRITERS; STAMPS
    • B41M—PRINTING, DUPLICATING, MARKING, OR COPYING PROCESSES; COLOUR PRINTING
    • B41M5/00—Duplicating or marking methods; Sheet materials for use therein
    • B41M5/26—Thermography ; Marking by high energetic means, e.g. laser otherwise than by burning, and characterised by the material used
    • B41M5/382—Contact thermal transfer or sublimation processes
    • B41M5/385—Contact thermal transfer or sublimation processes characterised by the transferable dyes or pigments
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B41—PRINTING; LINING MACHINES; TYPEWRITERS; STAMPS
    • B41M—PRINTING, DUPLICATING, MARKING, OR COPYING PROCESSES; COLOUR PRINTING
    • B41M5/00—Duplicating or marking methods; Sheet materials for use therein
    • B41M5/26—Thermography ; Marking by high energetic means, e.g. laser otherwise than by burning, and characterised by the material used
    • B41M5/382—Contact thermal transfer or sublimation processes
    • B41M5/392—Additives, other than colour forming substances, dyes or pigments, e.g. sensitisers, transfer promoting agents
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B41—PRINTING; LINING MACHINES; TYPEWRITERS; STAMPS
    • B41M—PRINTING, DUPLICATING, MARKING, OR COPYING PROCESSES; COLOUR PRINTING
    • B41M5/00—Duplicating or marking methods; Sheet materials for use therein
    • B41M5/26—Thermography ; Marking by high energetic means, e.g. laser otherwise than by burning, and characterised by the material used
    • B41M5/382—Contact thermal transfer or sublimation processes
    • B41M5/385—Contact thermal transfer or sublimation processes characterised by the transferable dyes or pigments
    • B41M5/3852—Anthraquinone or naphthoquinone dyes

Definitions

  • the present invention relates to thermal transfer printing wherein images are formed on a receiving substrate by heating extremely precise areas of a print ribbon with thin film resistors. This heating of the localized area causes transfer of ink or other sensible material from the ribbon to the receiving substrate.
  • Sensible material is typically a pigment or dye which can be detected optically or magnetically.
  • the present invention is directed to coating formulations (thermal transfer ink formulations) and thermal transfer media (ribbons) obtained therefrom which produce printed images with photochromic properties.
  • Thermal transfer printing has displaced impact printing in many applications due to advances such as the relatively low noise levels which are attained during the printing operation.
  • Thermal transfer printing is widely used in special applications such as in the printing of machine readable bar codes and magnetic alpha-numeric characters.
  • the thermal transfer process provides great flexibility in generating images and allows for broad variations in style, size and color of the printed image.
  • Photochromic compounds have been employed in various articles such as window glasses, sunglasses and films. It would be advantageous to provide images having photochromic properties (photochromism) which are generated by thermal transfer printing.
  • Photochromism means such characteristics of a material that the material develops a color under irradiation with excitation rays such as ultraviolet rays and returns to the initial uncolored state when allowing the material to stand. That is, photochromism means that the material is reversibly colored and discolored repeatedly.
  • a coating formulation for a thermal transfer layer which transfers an image basis to a receiving substrate when exposed to heat
  • said coating formulation comprises wax, binder resin, solvent and a sensible material which comprises a photochromic pigment, a mixture of photochromic pigments, a photochromic dye, a mixture of photochromic dyes or a combination of one or more photochromic pigments and one or more photochromic dyes in an amount sufficient to change the color of the image basis upon subsequent exposure to U.V. light.
  • thermo transfer medium comprising a flexible substrate and a thermal transfer layer positioned thereon, said layer having a softening point in the range of 40°C to 250°C, said layer comprises a coating formulation according to any preceding claim.
  • an article carrying an image basis said image basis changing colour when subsequently exposed to U.V. light so as to produce an image, characterized in that said image basis is produced from a thermal transfer medium.
  • Thermal transfer ribbon 20 comprises substrate 22 of a flexible material which is preferably a thin smooth paper or plastic-like material.
  • Tissue type paper materials such as 30-40 gauge capacitor tissue, manufactured by Glatz and polyester-type plastic materials such as 14-35 gauge polyester film manufactured by Dupont under the trademark Mylar® are suitable.
  • Polyethylene naphthalate films, polyamide films such as nylon, polyolefin films such as polypropylene film, cellulose films such as triacetate film and polycarbonate films are also suitable.
  • the substrates should have high tensile strength to provide ease in handling and coating and preferably provide these properties at minimum thickness and low heat resistance to prolong the life of heating elements within thermal print heads.
  • the thickness is preferably 3 to 10 ⁇ m.
  • the substrate or base film may be provided with a backcoating (not shown) on the surface opposite the thermal transfer layer.
  • thermal transfer layer 24 Positioned on substrate 22 is thermal transfer layer 24, also referred to as a functional layer.
  • the thermal sensitivity of thermal transfer layer 24 is determined by the softening point of the wax and binder resin therein.
  • This thermal transfer layer has a softening point below 250°C, preferably below 200°C and most preferably from 50°C to 125°C. Softening temperatures within this range enable the thermal transfer medium to be used in conventional thermal transfer printers, which typically have print heads which operate at temperatures in the range of 50°C to 300°C, more typically, temperatures in the range of 60°C to 125°C.
  • the thermal transfer layer 24 contains a wax and binder resin which are preferably compatible so that exposure to heat from print head 30 uniformly transfers thermal transfer layer 24 from substrate 22 to synthetic resin receiving substrate 28 and forms image 32.
  • the coating formulation of this invention comprises the components of conventional coating formulations such as one or more waxes, binder resins and solvents.
  • the sensible material (pigment or dye) employed is a photochromic dye, a mixture of photochromic dyes, a photochromic pigment, a mixture of photochromic pigments or a combination of one or more photochromic dyes and one or more photochromic pigments.
  • Photochromic compounds suitable for use in this invention are those classified as organic photochromic compounds. Many of such compounds are known to be homogeneously mixed with organic high molecular weight compounds in the preparation of photochromic films and laminates .
  • Suitable photochromic compounds include the spiro compounds of formula V disclosed by Takahashi et al. in U.S. Patent No. 5,266,447. These include spiroxazine compounds, spiropyran compounds and thiopyran compounds of the formulae in columns 5-6 of U.S. Patent No. 5,266,447.
  • photochromic compounds include the benzopyran compounds disclosed by Kumar in U.S. Patent No. 5,429,774, the benzothioxanthone oxides disclosed by Fischer et al. in U.S. Patent No. 5,177,218, the dinitrated spiropyrans disclosed by Hibino et al. in U.S. Patent No. 5,155,230, the naphthacenequinones disclosed by Fischer et al. in U.S. Patent No. 5,206,395 and U.S. Patent No. 5,407,885, the naphthopyran compounds disclosed by Knowles in U.S. Patent No.
  • the photochromic pigments/dyes are preferably added to the formulation in manner consistent with conventional methods for introducing conventional pigments or dyes. However, alternative (non-conventional) methods for preparing the coating formulations of this invention may also suitable.
  • the photochromic dye/pigment is employed in an amount sufficient to change the color of the thermal transfer layer formed therefrom when exposed U.V. light.
  • the photochromic dye/pigment is typically employed in an amount in the range of about .01 to 50 wt.%, preferably 0.1-25 wt.% based on the of dry components. More preferably the amount employed ranges from about 1 to 10 wt. % and most preferably about 1 wt. % based on dry components.
  • the coating formulation of the present invention can be prepared in conventional equipment.
  • the preferred method is to mix the solvent, wax components and binder resin at an elevated temperature, preferably about 65°C.
  • the photochromic pigment/dye is added and the resulting mixture mixed at an elevated temperature, preferably from about 60°C to 65°C.
  • the pigments are typically ground in an attritor.
  • the coating formulation comprises wax as a main dry component.
  • Suitable waxes provide temperature sensitivity and flexibility. Examples include natural waxes such as carnauba wax, rice bran wax, bees wax, lanolin, candelilla wax, motan wax and ceresine wax; petroleum waxes such as paraffin wax and microcrystalline waxes; synthetic hydrocarbon waxes such as low molecular weight polyethylene and Fisher-Tropsch wax; higher fatty acids such as lauric acid, myristic acid, palmitic acid, stearic acid and behenic acid; higher aliphatic alcohol such as stearyl alcohol and esters such as sucrose fatty acid esters, sorbitane fatty acid esters and amides.
  • the wax-like substances have a melting point less than 200°C and preferably from 40°C to 130°C.
  • the amount of wax in the coating formulation is preferably above 25 wt.% and most preferably ranges from 25 to 85 percent by weight, based on the weight of dry ingredients.
  • the coating formulation of this invention also comprises a binder resin.
  • Suitable binder resins are those conventionally used in coating formulations. These include thermoplastic resins and reactive resins such as epoxy resins.
  • thermoplastic binder resins include those described in U.S. Patent Nos. 5,240,781 and U.S. 5,348,348 which have a melting point of less than 300°C, preferably from 40°C to 225°C.
  • suitable thermoplastic resins include polyvinyl chloride, polyvinyl acetate, vinyl chloride-vinyl acetate copolymers, polyethylene, polypropylene, polyacetal, ethylene-vinyl acetate copolymers, ethylene alkyl (meth)acrylate copolymers, ethylene-ethyl acetate copolymers, polystyrene, styrene copolymers, polyamide, ethylcellulose, epoxy resin, xylene resin, ketone resin, petroleum resin, terpene resin, polyurethane resin, polyvinyl butyryl, styrene-butadiene rubber, saturated polyesters, styrene-alkyl (meth)acrylate copo
  • Suitable reactive binder components include epoxy resins and a polymerization initiator (crosslinker).
  • Suitable epoxy resins include those that have at least two oxirane groups such as epoxy novolak resins obtained by reacting epichlorohydrin with phenol/formaldehyde condensates or cresol/formaldehyde condensates.
  • Another preferred epoxy resin is polyglycidyl ether polymers obtained by reaction of epichlorohydrin with a polyhydroxy monomer such as 1,4 butanediol.
  • a specific example of suitable epoxy novolak resin is Epon 164 available from Shell Chemical Company.
  • a specific example of the polyglycidyl ether is available from Ciba-Geigy Corporation under the trade name Araldite® GT 7013.
  • the epoxy resins are preferably employed with a crosslinker which activates upon exposure to the heat from a thermal print head.
  • Preferred crosslinkers include polyamines with at least two primary or secondary amine groups. Examples being Epi-cure P101 and Ancamine 2014FG available from Shell Chemical Company and Air Products, respectively. Accelerators such as triglycidylisocyanurate can be used with the crosslinker to accelerate the reaction.
  • the epoxy resins typically comprise more than 25 wt.% of the coating formulation based on dry components in view of their low viscosity. Waxes are typically not necessary when reactive epoxy resins form the binder.
  • the solvents employed in coating formulations of this invention can vary widely and are dependent on the solubility of the binder resin.
  • a preferred solvent is mineral spirits.
  • Other suitable solvents include esters, ketones, ethers, alcohols, aliphatics and aromatics.
  • the solids content of the coating formulation is typically within the range of 15 to 100 wt.% (hot melt), depending on the viscosity of the dry components therein.
  • the coating formulation may also contain another sensible material or pigment in addition to the photochromic pigments/dye discussed above. These are preferably colorless pigments used as filler or light in color so as not to interfere with the photochromic effect.
  • the photochromic pigments may be used to change the color of light colored pigments.
  • the additional sensible material is typically a coloring agent, such as a dye or pigment or magnetic particles; however any coloring agent used in conventional ink ribbons is suitable, including carbon black and a variety of organic and inorganic coloring pigments and dyes, examples of which include phthalocyanine dyes, fluorescent naphthalimide dyes and others such as cadmium, primrose, chrome yellow, ultra marine blue, titanium dioxide, zinc oxide, iron oxide, cobalt oxide, nickel oxide, etc.
  • Examples of sensible materials include those described in U.S. 3,663,278 and U.S. 4,923,749. Reactive dyes such as leuco dyes are also suitable.
  • the thermal transfer layer includes a magnetic pigment or particles for use in imaging to enable optical human or machine reading of the characters.
  • the additional sensible material or pigment is typically used in an amount of from 0 to 40 parts by weight based on the total dry ingredients of the coating formulation.
  • the coating formulations may contain conventional additives such as plasticizers, viscosity modifiers, tackifiers, etc.
  • a preferred formulation is that containing a mixture of rice bran wax in an amount ranging from 60 to 95 wt.% based on the total dry ingredients, an ethyl vinyl acetate copolymer binder resin and the photochromic pigment.
  • Mineral spirits are a preferred solvent. This preferred formulation is made by mixing the solution of mineral spirits, rice bran wax and ethyl vinyl acetate copolymer binder resin for about 15 minutes at a temperature of about 65°C, after which the photochromic dye is added at about 60°C to 70°C for about two hours.
  • the thermal transfer ribbon of the present invention comprises a substrate as described above, preferably polyethylene terephthalate, and a thermal transfer layer comprised of wax, binder resin, sometimes residual solvent and a photochromic pigment.
  • the thermal transfer layer is preferably obtained from the coating formulation of the present invention. Suitable waxes, binder resins and photochromic pigments are as described above.
  • the thermal transfer layer (functional layer) preferably has a softening point within the range of about 50°C to 250°C which enables transfer at normal print head energies which range from about 100°C to 250°C and more typically from about 100°C to 150°C.
  • the thermal transfer ribbon of the present invention can be prepared from formulations of the present invention in the form of either a solution, dispersion or emulsion.
  • the ribbons can be prepared by conventional techniques and equipment such as a Meyer Rod or like wire round doctor bar set up on a conventional coating machine to provide the coating weights described above.
  • the coating weight of the thermal transfer layer typically ranges from 1.9 to 4.3 g/m 2 .
  • a temperature of about 65°C is maintained during the entire coating process.
  • the thermal transfer layer can be fully transferred onto a receiving substrate such as paper or synthetic resin at a temperature in the range of 75°C to 200°C.
  • the thermal transfer ribbon of the present invention provides the advantages of thermal printing.
  • the thermal transfer layer softens and transfers from the ribbon to the receiving substrate with some of the silicone resin backcoating therein.
  • the images of this invention are preferably derived from the thermal transfer ribbons of this invention and comprise a single layer of the wax, binder resin and photochromic pigments/dyes, as described above, transferred from the thermal transfer layer onto a substrate.
  • the images of this invention are preferably transparent until exposed to U.V. light which is achieved by excluding colored pigments.
  • the images can be patterned in fine detail as shown in Fig. 3, which is an image 100 of this invention in the pattern of a bar code. When transparent, this image enables the identification of goods or authentication of articles without disrupting the appearance/packaging of the goods or articles.
  • the image 100 can also be a decorative pattern for novelty items such as cards shirts, etc. as shown in Fig. 4.
  • a coating formulation of the present invention is prepared by mixing mineral spirits, wax and binder resin in the proportions indicated in Table 1 and heating the mixture to 60°C for 15 minutes.
  • a mixture of photochromic dyes available from Xytronyx Inc. in the amount indicated in Table 1 is added to the resultant mixture at a temperature of from about 140°F to 150°F for about 2 hours.
  • a thermal transfer medium of the present invention is prepared by coating a formulation as defined above onto a 4.5 ⁇ m Polyester Mylar Film by E. I. Dupont de Nemours & Co., Incorporated at a coat weight of from 1.9 to 4.3 g/m 2 .
  • the solution is coated onto the mylar film at 70°C using a doctor bar and subsequently dried.

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  • Physics & Mathematics (AREA)
  • Optics & Photonics (AREA)
  • Thermal Transfer Or Thermal Recording In General (AREA)
  • Impression-Transfer Materials And Handling Thereof (AREA)
  • Paints Or Removers (AREA)
EP97304195A 1996-06-27 1997-06-16 Compositions pour l'impression par transfert thermique Withdrawn EP0816116A1 (fr)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US67105296A 1996-06-27 1996-06-27
US671052 1996-06-27

Publications (1)

Publication Number Publication Date
EP0816116A1 true EP0816116A1 (fr) 1998-01-07

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EP97304195A Withdrawn EP0816116A1 (fr) 1996-06-27 1997-06-16 Compositions pour l'impression par transfert thermique

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EP (1) EP0816116A1 (fr)
JP (1) JPH10114156A (fr)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6613403B2 (en) * 1998-12-21 2003-09-02 Ncr Corporation Ink with near infrared fluorophores and U.V. absorbers
US7645719B2 (en) 2004-10-13 2010-01-12 Ncr Corporation Thermal paper with security features
WO2013063593A1 (fr) * 2011-10-27 2013-05-02 Chromatic Technologies, Inc. Encres photochromiques

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB2458262B (en) 2008-02-29 2012-11-07 Illinois Tool Works Improvements in thermal transfer printing
CN101850671B (zh) * 2010-05-31 2011-09-28 杭州天地数码科技有限公司 热熔涂布的混合基热转印色带及其生产方法

Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS6438283A (en) * 1987-08-05 1989-02-08 Toyo Ink Mfg Co Thermal transfer material
JPH0361084A (ja) * 1989-07-28 1991-03-15 Toyo Ink Mfg Co Ltd 感熱転写材
US5244524A (en) * 1990-04-09 1993-09-14 Brother Kogyo Kabushiki Kaisha Printing method for thermally transferring image section of print sheet to image receiving member
US5516590A (en) * 1993-07-15 1996-05-14 Ncr Corporation Fluorescent security thermal transfer printing ribbons

Patent Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS6438283A (en) * 1987-08-05 1989-02-08 Toyo Ink Mfg Co Thermal transfer material
JPH0361084A (ja) * 1989-07-28 1991-03-15 Toyo Ink Mfg Co Ltd 感熱転写材
US5244524A (en) * 1990-04-09 1993-09-14 Brother Kogyo Kabushiki Kaisha Printing method for thermally transferring image section of print sheet to image receiving member
US5516590A (en) * 1993-07-15 1996-05-14 Ncr Corporation Fluorescent security thermal transfer printing ribbons

Non-Patent Citations (2)

* Cited by examiner, † Cited by third party
Title
DATABASE WPI Section Ch Week 8912, Derwent World Patents Index; Class A89, AN 89-088805, XP002035860 *
DATABASE WPI Section Ch Week 9117, Derwent World Patents Index; Class A89, AN 91-121702, XP002035861 *

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6613403B2 (en) * 1998-12-21 2003-09-02 Ncr Corporation Ink with near infrared fluorophores and U.V. absorbers
US7645719B2 (en) 2004-10-13 2010-01-12 Ncr Corporation Thermal paper with security features
WO2013063593A1 (fr) * 2011-10-27 2013-05-02 Chromatic Technologies, Inc. Encres photochromiques
US9187668B2 (en) 2011-10-27 2015-11-17 Chromatic Technologies, Inc. Photochromic inks
US9738825B2 (en) 2011-10-27 2017-08-22 Chromatic Technologies, Inc. Photochromic inks

Also Published As

Publication number Publication date
JPH10114156A (ja) 1998-05-06

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