EP0111004A1 - Vaporizable dye composition and sheet containing same - Google Patents

Vaporizable dye composition and sheet containing same Download PDF

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Publication number
EP0111004A1
EP0111004A1 EP83901632A EP83901632A EP0111004A1 EP 0111004 A1 EP0111004 A1 EP 0111004A1 EP 83901632 A EP83901632 A EP 83901632A EP 83901632 A EP83901632 A EP 83901632A EP 0111004 A1 EP0111004 A1 EP 0111004A1
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EP
European Patent Office
Prior art keywords
dye
parts
binder
vaporizable
resin
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Withdrawn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
EP83901632A
Other languages
German (de)
French (fr)
Other versions
EP0111004A4 (en
Inventor
H. Dainichiseika Color & Chemi Nakano
Osamu Sony Corporation Majima
N. Dainichiseika Color & Chemi Fukushima
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.)
Dainichiseika Color and Chemicals Mfg Co Ltd
Sony Corp
Original Assignee
Dainichiseika Color and Chemicals Mfg Co Ltd
Sony Corp
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 Dainichiseika Color and Chemicals Mfg Co Ltd, Sony Corp filed Critical Dainichiseika Color and Chemicals Mfg Co Ltd
Publication of EP0111004A1 publication Critical patent/EP0111004A1/en
Publication of EP0111004A4 publication Critical patent/EP0111004A4/en
Withdrawn legal-status Critical Current

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Classifications

    • BPERFORMING OPERATIONS; TRANSPORTING
    • B41PRINTING; LINING MACHINES; TYPEWRITERS; STAMPS
    • B41MPRINTING, DUPLICATING, MARKING, OR COPYING PROCESSES; COLOUR PRINTING
    • B41M5/00Duplicating or marking methods; Sheet materials for use therein
    • B41M5/26Thermography ; Marking by high energetic means, e.g. laser otherwise than by burning, and characterised by the material used
    • B41M5/382Contact thermal transfer or sublimation processes
    • B41M5/392Additives, other than colour forming substances, dyes or pigments, e.g. sensitisers, transfer promoting agents
    • B41M5/395Macromolecular additives, e.g. binders

Definitions

  • the present invention relates to a vaporizable dye composition used to manufacture a dye carrier sheet material which is used to form on a printing paper a clear picture image of excellent resolution and a sheet containing the same.
  • a coupler used for such system is a dye which is vaporizable and dyed on the printing paper by heating.
  • this coupler is formed on the surface of a sheet base material such as paper or the like with a synthetic resin binder.
  • the above sheet material is superposed on the printing paper and then heated by a thermal print head in response to the picture signal.
  • the dye is vaporized and then transferred to the printing paper.
  • the present inventors succeeded in obtaining a vaporizable dye composition which'can obviate the above defects inherent in the prior art technique and which can make a dye carrier sheet.
  • the present invention relates to a vaporizable dye composition consisting of vaporizable dye, binder and solvent in which a part or whole of the binder is made of curable resin.
  • a vaporizable dye used in the present invention is an organic dye of a relatively small molecular weight (for example, about 200 to 400) which is contained much in a well-known sublimation dye and a dispersing dye. And, this vaporizable dye is vaporized from solid or liquid state at temperature ranging from approximately 100 to 200°C (under atmospheric pressure), which can be dyed on a hydrophobic synthetic resin material such as polyester, polypropyrene, acetate and the like.
  • One example of the binder used in the present invention is made of natural or synthetic resin material containing a reactive functional group and a curing agent.
  • the reactive functional group there are hydroxyl group, carboxyl group, amino group, isocianate group, epoxy group or the like which are main ones.
  • the resin material containing hydroxyl group there are cellulose derivative, gum arabic, tragacanth gum, starch derivative, alginic acid derivative, polyvinyl alcohol, polyvinyl alcohol derivative, acrylpolyol, alkyd resin and the like.
  • As the resin material containing carboxyl group there are alkyd resin, cellulose derivative,-polymer.or copolymer of unsaturated carboxylic acid.
  • the resin material containing amino group there are melamine resin, urea resin or the like.
  • the resin material containing isocianate group there are polyisocianate compounds of various kinds, isocianate terminated prepolymer and the like.
  • the resin material containing epoxy group there are various epoxy resins.
  • the above resin having the functional group which can be reacted with the functional group of the resin selected from the above resin materials can be used as the-curing agent as it is.
  • the curing agents formed of - various kinds of silane coupling agent, titanate coupling agent, zirconium chelate agent, aluminium chelate agent, metal compound such as Mg, Ca, Zn, Pb or the like, organic acid, inorganic acid, various kinds of inorganic and organic salts, metal soap, various kinds of polyamine and the like.
  • resin is made of monomer, prepolymer or polymer or a mixture of them which contain in its structure at least one polymerizable unsaturated double bonds. If necessary, such resin contains photo-polymerization initiator.
  • the binder in the present invention may be the above curable resin only. However, when such binder is the above curable resin only, if the curing is advanced too much thereafter, frequently the dye contained therein is not vaporized smoothly. Therefore, it is desired to vaporize the dye smoothly by properly adjusting the using amount of the curing agent or by adding the conventional thermo-plastic resin or proper plasticizers of various kinds to the above curable resin.
  • thermo-plastic resin there may be non-reactive cellulose derivative, vinyl polymer, polyester, polyamide and the like.
  • a well-known plasticizer may be used. When such thermo-plastic resin and plasticizer are used, its amount must be selected so as to share less than approximately 30 weight % of the whole amount of the binder. If it exceeds the above amount, the object of the present invention can not be attained sufficiently.
  • solvents of various kinds such as alcohol-series, ester-series, ketone-series, aromatic-series, aliphatic-series, naphthene-series, isoparafin-series and the like solely or as a mixture thereof.
  • composition according to the present invention is the same as described .above, and if necessary, various kinds of well-known additives and filler can be used.
  • the composition of the present invention is produced by mixing the above components at a suitable ratio and carrying out the ordinary dispersing treatment therefor.
  • the ratio of each component used in the composition is preferably selected such that the dye is approximately 1 to 20 weight %, the binder is approximately 2 to 40 weight % and the solvent is approximately 40 to 97 weight % for the total amount of 100 weight %.
  • the dye composition of the present invention is a liquid-phase composition and is then coated on desirably a sheet-like base material such as a thin paper with an amount ranging from approximately 0.1 to 2 g/m 2 (as the amount of dye) by well-known coating means such as blade coater, air knife coater, roll coater, curtain coater, bar coater, gravure coater and the like. Then, it is cured by heating and drying or irradiating the radiant energy, which is further heated, if necessary, to thereby produce the dye carrier sheet material. As described above, the binder contained in the composition is cross-linked and the resin is formed of three dimensional network structure.
  • the binder in the dye layer can be prevented from being softened excessively and being adhesive by the heating of the thermal print head.
  • the dye carrier sheet and the printing paper can be prevented from being bonded to each other excessively and also the binder itself can be prevented from being transferred to the printing paper thus a clear picture image being made.
  • an example of the most preferable curing binder which does not prevent the vaporization of the dye and is not bonded to the printing paper excessively was a mixture of cellulose-series derivative and melamine series resin.
  • the heating is not required upon curing thereof and the curing thereof are completed in several seconds to several minutes so that the fugacity of the vaporizable dye does not occur at all.
  • This binder is also preferable for the aspect of productivity.
  • KAYASET RED B manufactured by NIPPON KAYAKU CO., LTD.
  • 15 parts of cellulose acetate propyonate, 2 parts of silica, 73 parts of toluene and 3 parts of xylylene diisocianate are used to produce the vaporizable dye composition of the present invention.
  • PTB-67 which is the dye for blue color and manufactured by MITSUBISHI CHEMICAL INDUSTRIES CO., LTD., 15 parts of ethyl cellulose, 1 part of silica and 74 parts of toluene are mixed together, dispersed by a centrifugal mill and added with 2 parts of methylol melamine and 0.5 parts of paratoluene sulfonic acid, thus the vaporizable dye composition of the present invention being made.
  • KAYASET BLUE 906 manufactured by NIPPON KAYAKU CO., LTD.
  • 20 parts of epoxy resin, 30 parts of toluene, 38 parts of diacetone alcohol and 2 parts of silica are mixed, dispersed by an attrition mill and added with 5 parts of methylol'melamine and 2 parts by weight of diethylene triamine, thus the vaporizable dye composition of the present invention being made.
  • compositions of the present invention according to the examples 1 to 8 are used to thereby produce the dye carrier sheet materials under the conditions tabulated on the following table 1.
  • the comparative example 1 on the above table 1 is the example in which xylenediisocianate is not used in the afore-described example 2, while the comparative example 2 is the example in which methylol melamine and paratoluene sulfonic acid are not used in the afore-described example 4.

Abstract

A vaporizable dye composition for preparing heat- sensitive recording sheet forming images with excellent resolution on photographic paper, and a sheet containing it. The composition comprises a vaporizable dye, a binder, and a solvent, with part or the whole of the binder being a crosslinking resin.

Description

    TECHNICAL FIELD
  • The present invention relates to a vaporizable dye composition used to manufacture a dye carrier sheet material which is used to form on a printing paper a clear picture image of excellent resolution and a sheet containing the same.
  • BACKGROUND ART
  • In the prior art, such a system has been developed that a picture picked up by a video camera or a still picture and the like from a television receiver, a VTR, a video disc and a computer is directly reproduced with full color on a printing paper. A coupler used for such system is a dye which is vaporizable and dyed on the printing paper by heating. Generally, this coupler is formed on the surface of a sheet base material such as paper or the like with a synthetic resin binder. The above sheet material is superposed on the printing paper and then heated by a thermal print head in response to the picture signal. Thus, the dye is vaporized and then transferred to the printing paper. Although such sheet material coated with vaporizable dye is well known in the field of the heat transfer printing technique, such well-known sheet material can not be used as the dye carrier sheet material for the above system. The reasons are as follows. While in the conventional heat transfer printing system, the sheet material is superposed on the textile and then heated for a relatively long time, the above new system admits quite short time of heating,with a relatively high temperature. Also, the material to which the dye is transferred is not the textile material but the sheet material (the printing paper) with the smooth surface, so that the dye carrier sheet material is melted on the printing paper, alternatively, the dye as well as the binder itself is transferred to the printing paper. Thus, the resolution is lowered, the clearness of the picture is lost and it is difficult to present the gradation thereof.
  • DISCLOSURE OF INVENTION
  • After various vigorous researches for removing the above defects, the present inventors succeeded in obtaining a vaporizable dye composition which'can obviate the above defects inherent in the prior art technique and which can make a dye carrier sheet.
  • The present invention relates to a vaporizable dye composition consisting of vaporizable dye, binder and solvent in which a part or whole of the binder is made of curable resin.
  • BEST MODE FOR CARRYING OUT THE INVENTION
  • The present invention will be described in detail. A vaporizable dye used in the present invention is an organic dye of a relatively small molecular weight (for example, about 200 to 400) which is contained much in a well-known sublimation dye and a dispersing dye. And, this vaporizable dye is vaporized from solid or liquid state at temperature ranging from approximately 100 to 200°C (under atmospheric pressure), which can be dyed on a hydrophobic synthetic resin material such as polyester, polypropyrene, acetate and the like. In view of the chemical structure, it is made of mainly dye such as azo-series, anthraquinone- series, styryl-series, quinophthalol-series, nitrodiphenyl amine-series and so on.
  • One example of the binder used in the present invention is made of natural or synthetic resin material containing a reactive functional group and a curing agent. As the reactive functional group, there are hydroxyl group, carboxyl group, amino group, isocianate group, epoxy group or the like which are main ones. As the resin material containing hydroxyl group, there are cellulose derivative, gum arabic, tragacanth gum, starch derivative, alginic acid derivative, polyvinyl alcohol, polyvinyl alcohol derivative, acrylpolyol, alkyd resin and the like. As the resin material containing carboxyl group, there are alkyd resin, cellulose derivative,-polymer.or copolymer of unsaturated carboxylic acid. As the resin material containing amino group, there are melamine resin, urea resin or the like. As the resin material containing isocianate group, there are polyisocianate compounds of various kinds, isocianate terminated prepolymer and the like. As the resin material containing epoxy group, there are various epoxy resins.
  • As the curing agent which is used together with the resins as described above, the above resin having the functional group which can be reacted with the functional group of the resin selected from the above resin materials can be used as the-curing agent as it is. In addition, there can be used well-known curing agents formed of - various kinds of silane coupling agent, titanate coupling agent, zirconium chelate agent, aluminium chelate agent, metal compound such as Mg, Ca, Zn, Pb or the like, organic acid, inorganic acid, various kinds of inorganic and organic salts, metal soap, various kinds of polyamine and the like.
  • As an example of other curable resin which can be used in the present invention, there is a resin which is hardened or cross-linked by irradiation.of radiation energy such as ultraviolet rays, electron beam and the like. Such resin is made of monomer, prepolymer or polymer or a mixture of them which contain in its structure at least one polymerizable unsaturated double bonds. If necessary, such resin contains photo-polymerization initiator. These curable resins themselves are well known.
  • The binder in the present invention may be the above curable resin only. However, when such binder is the above curable resin only, if the curing is advanced too much thereafter, frequently the dye contained therein is not vaporized smoothly. Therefore, it is desired to vaporize the dye smoothly by properly adjusting the using amount of the curing agent or by adding the conventional thermo-plastic resin or proper plasticizers of various kinds to the above curable resin. As such well-known thermo-plastic resin, there may be non-reactive cellulose derivative, vinyl polymer, polyester, polyamide and the like. Moreover, a well-known plasticizer may be used. When such thermo-plastic resin and plasticizer are used, its amount must be selected so as to share less than approximately 30 weight % of the whole amount of the binder. If it exceeds the above amount, the object of the present invention can not be attained sufficiently.
  • As the solvent used in the present invention, there can be used, in addition to water, solvents of various kinds such as alcohol-series, ester-series, ketone-series, aromatic-series, aliphatic-series, naphthene-series, isoparafin-series and the like solely or as a mixture thereof.
  • The fundamental component of the composition according to the present invention is the same as described .above, and if necessary, various kinds of well-known additives and filler can be used.
  • The composition of the present invention is produced by mixing the above components at a suitable ratio and carrying out the ordinary dispersing treatment therefor. The ratio of each component used in the composition is preferably selected such that the dye is approximately 1 to 20 weight %, the binder is approximately 2 to 40 weight % and the solvent is approximately 40 to 97 weight % for the total amount of 100 weight %.
  • The dye composition of the present invention thus obtained is a liquid-phase composition and is then coated on desirably a sheet-like base material such as a thin paper with an amount ranging from approximately 0.1 to 2 g/m2 (as the amount of dye) by well-known coating means such as blade coater, air knife coater, roll coater, curtain coater, bar coater, gravure coater and the like. Then, it is cured by heating and drying or irradiating the radiant energy, which is further heated, if necessary, to thereby produce the dye carrier sheet material. As described above, the binder contained in the composition is cross-linked and the resin is formed of three dimensional network structure. In consequence, even when this dye carrier sheet is superposed on the printing paper and the vaporizable dye is transferred to the printing paper by the thermal print head driven in accordance with a video signal to provide a picture image, the binder in the dye layer can be prevented from being softened excessively and being adhesive by the heating of the thermal print head. And, the dye carrier sheet and the printing paper can be prevented from being bonded to each other excessively and also the binder itself can be prevented from being transferred to the printing paper thus a clear picture image being made.
  • According to the detailed researches done by the present inventors, it was found out that an example of the most preferable curing binder which does not prevent the vaporization of the dye and is not bonded to the printing paper excessively was a mixture of cellulose-series derivative and melamine series resin.
  • Particularly when a radiation curable resin is used as the-binder, the heating is not required upon curing thereof and the curing thereof are completed in several seconds to several minutes so that the fugacity of the vaporizable dye does not occur at all. This binder is also preferable for the aspect of productivity.
  • Now, the present invention will be described more specifically with reference to examples. In the description below, the reference of "part" or "%" is weight.
  • Example 1
  • 5 parts of KAYASET YELLOW AG (manufactured by NIPPON KAYAKU CO., LTD.), 3 parts of carboxymethyl cellulose, 4 parts of polyvinyl alcohol, 0.1 parts of antifoaming agent and 88 parts of water are mixed, dispersed in a ball mill and added with 1 part of methylol melamine (curing agent) and 0.1 part of ammonium chloride to provide the vaporizable dye composition of the present invention.
  • Example 2
  • 10 parts of KAYASET RED B (manufactured by NIPPON KAYAKU CO., LTD.), 15 parts of cellulose acetate propyonate, 2 parts of silica, 73 parts of toluene and 3 parts of xylylene diisocianate are used to produce the vaporizable dye composition of the present invention.
  • Example 3
  • Instead of the xylylene diisocianate in the example 2, 1 part of tetrabenzyltitanate is used. As the solvent, 50 parts of toluene and 23 parts of isopropyl alcohol are used and other components are selected to be the same as those in the example 2, thus the vaporizable dye composition of the present invention being made.
  • Example 4
  • 10 parts of PTB-67 (which is the dye for blue color and manufactured by MITSUBISHI CHEMICAL INDUSTRIES CO., LTD.,) 15 parts of ethyl cellulose, 1 part of silica and 74 parts of toluene are mixed together, dispersed by a centrifugal mill and added with 2 parts of methylol melamine and 0.5 parts of paratoluene sulfonic acid, thus the vaporizable dye composition of the present invention being made.
  • Example 5
  • 10 parts of KAYASET BLUE 906 (manufactured by NIPPON KAYAKU CO., LTD.), 20 parts of epoxy resin, 30 parts of toluene, 38 parts of diacetone alcohol and 2 parts of silica are mixed, dispersed by an attrition mill and added with 5 parts of methylol'melamine and 2 parts by weight of diethylene triamine, thus the vaporizable dye composition of the present invention being made.
  • Example 6
  • 10 parts of KAYASET YELLOW AG, 50 parts of polyester acrylate, 5 parts of silica and 35 parts of toluene are mixed together and dispersed by a sand mill to thereby produce the vaporizable dye composition of the present invention.
  • Example 7
  • 10 parts of KAYASET RED B (manufactured by NIPPON KAYAKU CO., LTD.),`60 parts of trimethylolpropane triacrylate, 3 parts of benzophenone, 3 parts of methyldiethanol amine, 2 parts of silica and 22 parts of xylene are mixed together and dispersed by the attrition mill to thereby produce the vaporizable dye composition of the present invention.
  • Example 8
  • 10 parts of PTB-67, 20 parts of polyester acrylate, 10 parts of cellulose acetate propyonate, 1 part of benzoinisobutylether, 19 parts of isopropyl alcohol and 40 parts of toluene are used to produce the vaporizable dye composition of the present invention in the same way as in the example 7.
  • Example of use
  • The compositions of the present invention according to the examples 1 to 8 are used to thereby produce the dye carrier sheet materials under the conditions tabulated on the following table 1.
    Figure imgb0001
  • The comparative example 1 on the above table 1 is the example in which xylenediisocianate is not used in the afore-described example 2, while the comparative example 2 is the example in which methylol melamine and paratoluene sulfonic acid are not used in the afore-described example 4.

Claims (10)

1. A vaporizable dye composition comprising a vaporizable dye, a binder and a solvent in which said binder is partly or fully made of a curable resin.
2. A vaporizable dye composition according to claim 1, wherein said curable resin is made of natural or synthetic resin containing a reactive functional group and a curing agent.
3. A vaporizable dye composition according to claim 1, wherein said curable resin is a radiation curable resin.
4. A vaporizable dye composition according to claim 1, wherein the amount of said binder is selected to be 2 to 40 parts by weight relative to 1 to 20 parts by weight of vaporizable dye.
5. A dye carrier sheet comprising a base material and a dye layer formed on said base material and containing a vaporizable dye, said dye layer consisting of mainly a vaporizable dye and a binder and at least a part of said binder being made of a curable resin.
6. A dye carrier sheet according to claim 5, wherein said curable resin is made of a natural or synthetic resin containing a reactive functional group and a curing agent.
7. A dye carrier sheet according to claim 5, wherein said curable resin is a radiation curable resin.
8. A dye carrier sheet according to claim 5, wherein the amount of said binder is selected to be 2 to 40 parts by weight relative to 1 to 20 parts by weight of the vaporizable dye.
9. A vaporizable dye composition according to claim 1, wherein less than 30 weight % in the whole amount of said binder is thermoplastic resin.
10. A dye carrier sheet according to claim 5, wherein less than 30 weight % in the whole amount of said binder is thermoplastic resin.
EP19830901632 1982-06-08 1983-05-27 Vaporizable dye composition and sheet containing same. Withdrawn EP0111004A4 (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
JP98230/82 1982-06-08
JP57098230A JPS58215397A (en) 1982-06-08 1982-06-08 Volatile coloring matter composition

Publications (2)

Publication Number Publication Date
EP0111004A1 true EP0111004A1 (en) 1984-06-20
EP0111004A4 EP0111004A4 (en) 1985-06-06

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EP19830901632 Withdrawn EP0111004A4 (en) 1982-06-08 1983-05-27 Vaporizable dye composition and sheet containing same.

Country Status (3)

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EP (1) EP0111004A4 (en)
JP (1) JPS58215397A (en)
WO (1) WO1983004394A1 (en)

Cited By (25)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS61227092A (en) * 1985-04-01 1986-10-09 Mitsubishi Chem Ind Ltd Azo dyestuff for thermal transfer recording
US4725284A (en) * 1985-07-23 1988-02-16 Imperial Chemical Industries Plc Thermal transfer printing with z-alkyl-phenoxy anthraquinone dye mixture
US4822643A (en) * 1987-06-30 1989-04-18 Minnesota Mining And Manufacturing Company Thermal transfer imaging system
US4859651A (en) * 1987-08-04 1989-08-22 Imperial Chemical Industries Plc Thermal transfer printing
US4939118A (en) * 1988-06-15 1990-07-03 Basf Aktiengesellschaft Transfer of azo dyes having a pyridine coupling component
US4940692A (en) * 1988-04-12 1990-07-10 Basf Aktiengesellschaft Transfer of dyes
US5037798A (en) * 1988-05-31 1991-08-06 Basf Aktiengesellschaft Transfer of AZO dyes
EP0444325A1 (en) * 1990-03-01 1991-09-04 Agfa-Gevaert N.V. Modified dextran binder for use in thermal dye transfer
US5079365A (en) * 1989-09-07 1992-01-07 Basf Aktiengesellschaft Triazolopyridine dyes and thermal transfer of methine dyes
US5101035A (en) * 1989-08-26 1992-03-31 Basf Aktiengesellschaft Merocyanine-like thiazole dyes and thermal transfer thereof
US5118658A (en) * 1989-10-26 1992-06-02 Dai Nippon Insatsu Kabushiki Kaisha Heat transfer sheet
US5132438A (en) * 1990-02-15 1992-07-21 Basf Aktiengesellschaft Bichromophoric methine and azamethine dyes and process for transferring them
US5151506A (en) * 1989-08-16 1992-09-29 Basf Aktiengesellschaft Phenoneazo dyes
US5155089A (en) * 1990-12-14 1992-10-13 Basf Aktiengesellschaft Anthraquinone dyes for thermal transfer printing
US5202176A (en) * 1989-10-04 1993-04-13 Dai Nippon Insatsu Kabushiki Kaisha Heat transfer recording materials
US5281572A (en) * 1990-02-15 1994-01-25 Basf Aktiengesellschaft Bichromorphic methine and azamethine dyes and process for transferring them
US5312926A (en) * 1990-03-30 1994-05-17 Basf Aktiengesellschaft Indonaphthol dyes and thermal transfer thereof
US5352653A (en) * 1994-02-16 1994-10-04 Eastman Kodak Company Crosslinked dye-donor binder for thermal dye transfer systems
US5369079A (en) * 1989-10-04 1994-11-29 Dai Nippon Insatsu Kabushiki Kaisha Process for making a heat-transferred imaged article
US5371266A (en) * 1990-02-15 1994-12-06 Basf Aktiengesellschaft Bichromophoric cyano-containing methine dyes and transfer thereof
EP0701907A1 (en) 1994-09-13 1996-03-20 Agfa-Gevaert N.V. A dye donor element for use in a thermal dye transfer process
EP0792757A1 (en) 1996-02-27 1997-09-03 Agfa-Gevaert N.V. Dye donor element for use in thermal transfer printing
EP0798128A1 (en) * 1996-03-25 1997-10-01 Ncr International Inc. Thermal transfer medium with phase isolated reactive components
GB2325529A (en) * 1997-05-21 1998-11-25 Ncr Int Inc Thermal transfer medium
US6790493B2 (en) 2001-12-21 2004-09-14 Ncr Corporation Epoxy curing agent emulsification for TTR application

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Cited By (31)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH0513077B2 (en) * 1985-04-01 1993-02-19 Mitsubishi Chem Ind
JPS61227092A (en) * 1985-04-01 1986-10-09 Mitsubishi Chem Ind Ltd Azo dyestuff for thermal transfer recording
US4725284A (en) * 1985-07-23 1988-02-16 Imperial Chemical Industries Plc Thermal transfer printing with z-alkyl-phenoxy anthraquinone dye mixture
US4822643A (en) * 1987-06-30 1989-04-18 Minnesota Mining And Manufacturing Company Thermal transfer imaging system
US4859651A (en) * 1987-08-04 1989-08-22 Imperial Chemical Industries Plc Thermal transfer printing
US4940692A (en) * 1988-04-12 1990-07-10 Basf Aktiengesellschaft Transfer of dyes
US5037798A (en) * 1988-05-31 1991-08-06 Basf Aktiengesellschaft Transfer of AZO dyes
US4939118A (en) * 1988-06-15 1990-07-03 Basf Aktiengesellschaft Transfer of azo dyes having a pyridine coupling component
US5151506A (en) * 1989-08-16 1992-09-29 Basf Aktiengesellschaft Phenoneazo dyes
US5101035A (en) * 1989-08-26 1992-03-31 Basf Aktiengesellschaft Merocyanine-like thiazole dyes and thermal transfer thereof
US5079365A (en) * 1989-09-07 1992-01-07 Basf Aktiengesellschaft Triazolopyridine dyes and thermal transfer of methine dyes
US5369079A (en) * 1989-10-04 1994-11-29 Dai Nippon Insatsu Kabushiki Kaisha Process for making a heat-transferred imaged article
US5202176A (en) * 1989-10-04 1993-04-13 Dai Nippon Insatsu Kabushiki Kaisha Heat transfer recording materials
US5118658A (en) * 1989-10-26 1992-06-02 Dai Nippon Insatsu Kabushiki Kaisha Heat transfer sheet
US5132438A (en) * 1990-02-15 1992-07-21 Basf Aktiengesellschaft Bichromophoric methine and azamethine dyes and process for transferring them
US5371266A (en) * 1990-02-15 1994-12-06 Basf Aktiengesellschaft Bichromophoric cyano-containing methine dyes and transfer thereof
US5281572A (en) * 1990-02-15 1994-01-25 Basf Aktiengesellschaft Bichromorphic methine and azamethine dyes and process for transferring them
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EP0111004A4 (en) 1985-06-06
JPS58215397A (en) 1983-12-14
WO1983004394A1 (en) 1983-12-22

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