EP0268202A2 - Thermal transfer ink - Google Patents

Thermal transfer ink Download PDF

Info

Publication number
EP0268202A2
EP0268202A2 EP19870116658 EP87116658A EP0268202A2 EP 0268202 A2 EP0268202 A2 EP 0268202A2 EP 19870116658 EP19870116658 EP 19870116658 EP 87116658 A EP87116658 A EP 87116658A EP 0268202 A2 EP0268202 A2 EP 0268202A2
Authority
EP
European Patent Office
Prior art keywords
viscosity
resin
thermal transfer
wax
solvent
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.)
Granted
Application number
EP19870116658
Other languages
German (de)
French (fr)
Other versions
EP0268202A3 (en
EP0268202B1 (en
Inventor
Shinichiro Yamaguchi
Koichi Sakai
Hiroshi Yashima
Masanori Minato
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.)
Kao Corp
Original Assignee
Kao 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 Kao Corp filed Critical Kao Corp
Publication of EP0268202A2 publication Critical patent/EP0268202A2/en
Publication of EP0268202A3 publication Critical patent/EP0268202A3/en
Application granted granted Critical
Publication of EP0268202B1 publication Critical patent/EP0268202B1/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

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
    • 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

Definitions

  • the present invention relates to a thermal transfer ink necessary to a thermal transfer printer which is expanding the fields of application thereof because it is inexpensive, generates little noize, and is easy to handle.
  • Waxes such as paraffin and carnauba wax are predominantly used as the binders of conventional thermal transfer inks, which have a significantly low melt viscosity.
  • a clear print having a gloss peculiar to thermal transfer can be obtained.
  • various requirements involving printing on a paper having a less surface smoothness printing giving a fast print, printing at a high speed, and repeated printing.
  • the conven­tional ink constituted of wax alone cannot cope with the requirements. Therefore, investigations on inks comprising a resin as the main component are being made in various fields.
  • Known resins include one which promises application to the printing on a paper having a rough surface because of its high cohesive force and high capability of forming film, one which promises application to the printing giving a fast print because of its high strength, one which promises application to the printing with a high transfer sensitivity because of its amorphousness, and one which promises application to the repeated printing because of its strong adhesion.
  • a possibility of application of a resin to a thermal transfer has been developed.
  • resins have a very high melt viscosity as compared with waxes. This tendency is particularly remarkable when they are formed into an ink. In the thermal transfer system, this melt viscosity is an important factor determining formation of a transferred image, thus directly influencing the quality of a print.
  • a resin ink has a low viscosity comparable to that of a wax ink in a heat-molten state, a sufficient contact area is secured, thus achieving printing with a high coverage.
  • an ink containing a resin having a melting point suitable for thermal transfer as the main component does not generally have a low viscosity comparable to that of a wax when thermal transfer is carried out.
  • the inventors of the present invention have made intensive investigations with a view to solving the above-mentioned problems, and as a result, have found that a thermal transfer ink having excellent perform­ances in printing can be obtained by adding an adequate viscosity depressant according to the purpose to any one of various hot-melt resins which have been incapable of being employed because of their high melting points, thereby adjusting the viscosity.
  • a thermal transfer ink having excellent perform­ances in printing can be obtained by adding an adequate viscosity depressant according to the purpose to any one of various hot-melt resins which have been incapable of being employed because of their high melting points, thereby adjusting the viscosity.
  • the present invention has been completed.
  • a thermal transfer ink of a solution type comprising a resin having a melt viscosity of 10,000 to 1,000,000 cps (as measured at 120°C) as the base binder, characterized by containing 5 to 250 parts by weight, based on 100 parts by weight of the base resin, of at least one viscosity depressant selected from the group consisting of resins, waxes, higher fatty acids, higher alcohols, and synthetic esters for the purpose of lowering the melt viscosity, said viscosity depressant having a melt viscosity of 1 to 600 cps, measured at 120°c, and being insoluble in a solvent to use or so partially soluble in the solvent that more than 1 gram of the viscosity depressant may not be soluble in 100 grams of the solvent at 40°c.
  • An ink composition of the invention is useful for the thermal transfer and comprises 100 parts by weight of the above defined high viscosity-having resin and 5 to 250 parts by weight of the above defined viscosity depressant or thinner.
  • the ink composition further comprises a solvent and then the insoluble portion of the depressant stands in the form of fine particles in the emulsion or the slurry. It may contain the solvent in a conventional amount and a coloring matter.
  • the thermal transfer ink of the present invention is obtained by adding a viscosity depressant such as a low-viscosity resin or a wax to a thermal transfer ink having a relatively high melt viscosity and using a resin as the base binder in order to use the thermal transfer ink by lowering its viscosity.
  • a thermal transfer ink obtained by adding a partial insoluble portion of a viscosity depressant such as a wax in the particulate form such as an emulsion, a slurry or a fine powder to a solution type ink.
  • the thermal transfer ink of the present invention is applied to a base with a conventional means such as a gravure coater and dried to obtain a thermal transfer ink sheet without the need of paying attention to the compatibility of a high-viscosity resin with a viscosity depressant such as a wax.
  • any combination of a high-viscosity base resin and a viscosity depressant such as a wax is possible, and any high-­viscosity resin can be used as the thermal transfer ink binder.
  • a resin which can be used as the base binder in the present invention has a melt viscosity of 10,000 to 1,000,000 cps., measured at 120°c.
  • a resin include polyester, polyamide, acrylic, polysty­rene, polystyrene-acrylic, polyvinyl chloride, polyvinyl butyral, epoxy, ethylene-vinyl acetate, polyurethane and polycarbonate resins, and mixtures thereof, said resins having melting points of 60 to 120°C.
  • the viscosity depressant having a low viscosity which can be used in the present invention is at least one member selected from the group consisting of resins, waxes, higher fatty acids, higher alcohols, and synthetic esters, which have a melt viscosity of 1 to 600 cps, measured at 120°c, and being insoluble in a solvent to use or so partially soluble in the solvent that more than 1 gram of the viscosity depressant may not be soluble in 100 grams of the solvent at 40°c. More preferred are resins, waxes, higher fatty acids, higher alcohols, and synthetic esters which have a melt viscosity of 1 to 400 cps at 120°C.
  • any resin can be used as the low-viscosity resin in the present invention in so far as it has a low viscosity.
  • resins include polyethylene, polyester, ketone, ethylene- ⁇ -olefin copolymer ⁇ -olefin-maleic anhydride copolymer resins.
  • waxes can be mentioned as the wax that may be used in the present invention.
  • the waxes include natural plant waxes such as carnauba wax, candelilla wax, ouricury wax, sugarcane wax, and Japan wax; natural animal waxes such as bees­wax, spermaceti, Chinese wax, and wool wax; petroleum waxes such as paraffin wax, microcrystalline wax, oxidized paraffin wax, and oxidized microcrystalline wax; mineral waxes such as montan wax, ozokerite, ceresine, and lignite wax; synthetic waxes such as ketone wax, Fischer-Tropsch wax, castor wax, opal wax, Armor wax, and Acra wax; and modifications thereof.
  • Any higher fatty acid which is usually used can be used in the present invention.
  • Examples of such a higher fatty acid include palmitic acid, stearic acid, margaric acid, and behenic acid.
  • Any higher alcohol can be used in the present invention.
  • Examples of such a higher alcohol include palmityl alcohol, stearyl alcohol, behenyl alcohol, margaryl alcohol, myricyl alcohol, and eicosanol.
  • Examples of synthetic esters that may be used in the present invention include monoesters synthesized from the above-mentioned higher fatty acid and higher alcohol, diesters synthesized from a bifunctional dicarboxylic acid and the above-mentioned higher alcohol, and diesters synthesized from a bifunctional diol and the above-mentioned higher fatty acid.
  • Any solvent which is usually used in an ink or a coating can be used in the present invention.
  • a solvent include alcohols such as ethanol and isopropyl alcohol; ketones such as methyl ethyl ketone and methyl isobutyl ketone; aromatic solvents such as toluene and xylene; and water. These solvents may be used in mixture if necessary.
  • a thermal transfer ink sheet can be produced from the thermal transfer ink of the present invention by applying at least one layer of the thermal transfer ink of the present invention to a base or a coating layer on a base and drying it.
  • a combination of the thermal transfer ink layer with a top coat, a resistance layer for heating by passing electricity therethrough, or an electrically conductive layer may be employed.
  • the thermal transfer ink of the present invention is usually applied to a base with a coater or a printer.
  • a viscosity depressant added is not soluble in a solvent used at all, the interaction between precipitated particles becomes so strong that the structural viscosity is increased, whereby problems of separation of the ink from the gravure meshes in coating or printing and levelling just after the application are presented. Thus, any clean coating film can hardly be obtained.
  • a viscosity depressant to be added is at least partially soluble in a solvent used, so that the structural viscosity can be suppressed. As a result, good applicability or printability is attained.
  • a thermal transfer ink 1 of a solvent type comprising a polyester resin having a softening point of 90°C (melt viscosity at 120°C: 23,000 cps) as the main component and having the following composition was prepared:
  • a solution of a carnauba wax slurry 1 in toluene was prepared.
  • this slurry may be one prepared by completely dissolving carnauba wax in hot toluene and cooling the solution, or a slurry prepared by adding a fine carnauba wax powder and, if necessary, dispersing the mixture.
  • the obtained thermal transfer ink sheet was evaluated as regards obtained prints by using a commercially available thermal transfer printer.
  • the evaluation results are summarized in Table 1. It can be understood from the results that, with an increase in the amount of the carnauba wax slurry, a visocisty lowering effect was developed, whereby a thermally transferred image having a transfer rate and a resolution comparable to those of a wax ink was obtained while keeping the features of the resin, such as fastness.
  • a thermally transferred image was obtained under the same conditions as those of Example 1 by using the ink 1.
  • Solution type inks each comprising as the main component a polyamide resin having a softening point of 86°C (melt viscosity at 120°C: 17,500 cps), a polystyrene­ acrylic resin having a softening point of 102°C (melt viscosity at 120°c: 50,000 cps), or a polystyrene resin having a softening point of 78°C (melt viscosity at 120°c: 11,000 cps) (in a 1/1 solvent mixture of toluene and methyl ethyl ketone) were admixed with 10, 20, 30, 40, and 50%, based on the resin, of a mixed slurry composed of polyethylene wax (melt viscosity at 120°C: 30 cps) and carnauba wax prepared at a ratio of 1:1 in the same manner as that of Example 1 to prepare inks.
  • a slurry of paraffin wax having a melting point of 105°C (melt viscosity at 120°C: 23 cps) in toluene was prepared.
  • the same polyester resin as that described in Example 1 was admixed with 30%, based on the weight of the resin, of the slurry.
  • the evaluation of the obtained prints was made in the same manner as that of Example 1 to obtain results as shown in Table 3.
  • a polyamide resin having a softening point of 106°C (melt viscosity at 120°C: 120,000) was emulsified by the ordinary method to prepare an emulsion ink.
  • a modified microcrystalline wax having a melting point of 87°C (melt viscosity at 120°C: 4 cps) was emulsified with a common emulsifier to prepare an emulsion. 20%, based on the weight of the resin, of the emulsion was added to the above-­ mentioned emulsion ink. Evaluation of the obtained prints was made in the same manner as that of Example 1 to obtain results as shown in Table 3.
  • Example 2 The same resin ink as that used in Example 1 was admixed with 30%, based on the resin, of a polyester resin having a melting point of 78°C (melt viscosity at 120°C: 2,300 cps) to prepare an ink. Evaluation of the obtained prints was made in the same manner as that of Example 1 to obtain results as shown in Table 3.

Landscapes

  • Physics & Mathematics (AREA)
  • Optics & Photonics (AREA)
  • Inks, Pencil-Leads, Or Crayons (AREA)
  • Impression-Transfer Materials And Handling Thereof (AREA)
  • Thermal Transfer Or Thermal Recording In General (AREA)

Abstract

A thermal transfer ink of a solution type comprises a resin having a melt viscosity of 10,000 to 1,000,000 cps (as measured at 120°C) as the base binder, characterized by containing 5 to 250 parts by weight, based on 100 parts by weight of the base resin, of at least one viscosity depressant selected from the group consisting of resins, waxes, higher fatty acids, higher alcohols, and synthetic esters for the purpose of lowering the melt viscosity, said viscosity depres­sant having a melt viscosity of 1 to 600 cps, measured at 120°c, and being insoluble in a solvent to use or so partially soluble in the solvent that more than 1 gram of the viscosity depressant may not be soluble in 100 grams of the solvent at 40°c.

Description

  • The present invention relates to a thermal transfer ink necessary to a thermal transfer printer which is expanding the fields of application thereof because it is inexpensive, generates little noize, and is easy to handle.
  • [Prior Art and the Problems thereof]
  • Waxes such as paraffin and carnauba wax are predominantly used as the binders of conventional thermal transfer inks, which have a significantly low melt viscosity. Thus, when printing is made on a thermal transfer paper having a good smoothness, a clear print having a gloss peculiar to thermal transfer can be obtained. With expansion of the application field, however, there have arisen various requirements involving printing on a paper having a less surface smoothness, printing giving a fast print, printing at a high speed, and repeated printing. Thus, as the level of requirements is enhanced, the conven­tional ink constituted of wax alone cannot cope with the requirements. Therefore, investigations on inks comprising a resin as the main component are being made in various fields.
  • Known resins include one which promises application to the printing on a paper having a rough surface because of its high cohesive force and high capability of forming film, one which promises application to the printing giving a fast print because of its high strength, one which promises application to the printing with a high transfer sensitivity because of its amorphousness, and one which promises application to the repeated printing because of its strong adhesion. Thus, a possibility of application of a resin to a thermal transfer has been developed. In general, however, resins have a very high melt viscosity as compared with waxes. This tendency is particularly remarkable when they are formed into an ink. In the thermal transfer system, this melt viscosity is an important factor determining formation of a transferred image, thus directly influencing the quality of a print. If a resin ink has a low viscosity comparable to that of a wax ink in a heat-molten state, a sufficient contact area is secured, thus achieving printing with a high coverage. However, an ink containing a resin having a melting point suitable for thermal transfer as the main component does not generally have a low viscosity comparable to that of a wax when thermal transfer is carried out.
  • In order to enable the use of a high-viscosity resin ink by lowering its viscosity, a countermeasure such as addition of an oil (e.g. butyl cellosolve or spindle oil) has heretofore been adopted. However, this method presents problems of bleeding out and blocking during storage. Thus, a difficulty is experienced in adding an amount of oil enough to secure a sufficiently low viscosity.
  • Summary of the Invention
  • The inventors of the present invention have made intensive investigations with a view to solving the above-mentioned problems, and as a result, have found that a thermal transfer ink having excellent perform­ances in printing can be obtained by adding an adequate viscosity depressant according to the purpose to any one of various hot-melt resins which have been incapable of being employed because of their high melting points, thereby adjusting the viscosity. Thus the present invention has been completed.
  • Specifically, in accordance with the present invention, there is provided a thermal transfer ink of a solution type comprising a resin having a melt viscosity of 10,000 to 1,000,000 cps (as measured at 120°C) as the base binder, characterized by containing 5 to 250 parts by weight, based on 100 parts by weight of the base resin, of at least one viscosity depressant selected from the group consisting of resins, waxes, higher fatty acids, higher alcohols, and synthetic esters for the purpose of lowering the melt viscosity, said viscosity depressant having a melt viscosity of 1 to 600 cps, measured at 120°c, and being insoluble in a solvent to use or so partially soluble in the solvent that more than 1 gram of the viscosity depressant may not be soluble in 100 grams of the solvent at 40°c.
  • An ink composition of the invention is useful for the thermal transfer and comprises 100 parts by weight of the above defined high viscosity-having resin and 5 to 250 parts by weight of the above defined viscosity depressant or thinner.
  • It is preferable that the ink composition further comprises a solvent and then the insoluble portion of the depressant stands in the form of fine particles in the emulsion or the slurry. It may contain the solvent in a conventional amount and a coloring matter.
  • The thermal transfer ink of the present invention is obtained by adding a viscosity depressant such as a low-viscosity resin or a wax to a thermal transfer ink having a relatively high melt viscosity and using a resin as the base binder in order to use the thermal transfer ink by lowering its viscosity. Particularly preferred is a thermal transfer ink obtained by adding a partial insoluble portion of a viscosity depressant such as a wax in the particulate form such as an emulsion, a slurry or a fine powder to a solution type ink.
  • The thermal transfer ink of the present invention is applied to a base with a conventional means such as a gravure coater and dried to obtain a thermal transfer ink sheet without the need of paying attention to the compatibility of a high-viscosity resin with a viscosity depressant such as a wax.
  • According to the present invention, any combination of a high-viscosity base resin and a viscosity depressant such as a wax is possible, and any high-­viscosity resin can be used as the thermal transfer ink binder.
  • A resin which can be used as the base binder in the present invention has a melt viscosity of 10,000 to 1,000,000 cps., measured at 120°c. Examples of such a resin include polyester, polyamide, acrylic, polysty­rene, polystyrene-acrylic, polyvinyl chloride, polyvinyl butyral, epoxy, ethylene-vinyl acetate, polyurethane and polycarbonate resins, and mixtures thereof, said resins having melting points of 60 to 120°C.
  • The viscosity depressant having a low viscosity which can be used in the present invention is at least one member selected from the group consisting of resins, waxes, higher fatty acids, higher alcohols, and synthetic esters, which have a melt viscosity of 1 to 600 cps, measured at 120°c, and being insoluble in a solvent to use or so partially soluble in the solvent that more than 1 gram of the viscosity depressant may not be soluble in 100 grams of the solvent at 40°c.
    More preferred are resins, waxes, higher fatty acids, higher alcohols, and synthetic esters which have a melt viscosity of 1 to 400 cps at 120°C.
  • Any resin can be used as the low-viscosity resin in the present invention in so far as it has a low viscosity. Examples of such resins include polyethylene, polyester, ketone, ethylene-α-olefin copolymer α-olefin-maleic anhydride copolymer resins.
  • All kinds of waxes can be mentioned as the wax that may be used in the present invention. Examples of the waxes include natural plant waxes such as carnauba wax, candelilla wax, ouricury wax, sugarcane wax, and Japan wax; natural animal waxes such as bees­wax, spermaceti, Chinese wax, and wool wax; petroleum waxes such as paraffin wax, microcrystalline wax, oxidized paraffin wax, and oxidized microcrystalline wax; mineral waxes such as montan wax, ozokerite, ceresine, and lignite wax; synthetic waxes such as ketone wax, Fischer-Tropsch wax, castor wax, opal wax, Armor wax, and Acra wax; and modifications thereof.
  • Any higher fatty acid which is usually used can be used in the present invention. Examples of such a higher fatty acid include palmitic acid, stearic acid, margaric acid, and behenic acid.
  • Any higher alcohol can be used in the present invention. Examples of such a higher alcohol include palmityl alcohol, stearyl alcohol, behenyl alcohol, margaryl alcohol, myricyl alcohol, and eicosanol.
  • Examples of synthetic esters that may be used in the present invention include monoesters synthesized from the above-mentioned higher fatty acid and higher alcohol, diesters synthesized from a bifunctional dicarboxylic acid and the above-mentioned higher alcohol, and diesters synthesized from a bifunctional diol and the above-mentioned higher fatty acid.
  • Any solvent which is usually used in an ink or a coating can be used in the present invention. Examples of such a solvent include alcohols such as ethanol and isopropyl alcohol; ketones such as methyl ethyl ketone and methyl isobutyl ketone; aromatic solvents such as toluene and xylene; and water. These solvents may be used in mixture if necessary.
  • A thermal transfer ink sheet can be produced from the thermal transfer ink of the present invention by applying at least one layer of the thermal transfer ink of the present invention to a base or a coating layer on a base and drying it. A combination of the thermal transfer ink layer with a top coat, a resistance layer for heating by passing electricity therethrough, or an electrically conductive layer may be employed.
  • The thermal transfer ink of the present invention is usually applied to a base with a coater or a printer. When a viscosity depressant added is not soluble in a solvent used at all, the interaction between precipitated particles becomes so strong that the structural viscosity is increased, whereby problems of separation of the ink from the gravure meshes in coating or printing and levelling just after the application are presented. Thus, any clean coating film can hardly be obtained. According to the present invention, however, a viscosity depressant to be added is at least partially soluble in a solvent used, so that the structural viscosity can be suppressed. As a result, good applicability or printability is attained.
  • [Examples]
  • The following Examples will further exemplify the effectiveness of the present invention, but should not be construed as limiting the scope of the invention.
  • Example 1
  • A thermal transfer ink ① of a solvent type comprising a polyester resin having a softening point of 90°C (melt viscosity at 120°C: 23,000 cps) as the main component and having the following composition was prepared:
    Figure imgb0001
  • Separately, a solution of a carnauba wax slurry ① in toluene was prepared. From the aspect of performance, this slurry may be one prepared by completely dissolving carnauba wax in hot toluene and cooling the solution, or a slurry prepared by adding a fine carnauba wax powder and, if necessary, dispersing the mixture.
    Figure imgb0002
  • Inks
    Figure imgb0003
    to
    Figure imgb0004
    were prepared by adding the slurry
    Figure imgb0005
    to the ink
    Figure imgb0006
    .
    Figure imgb0007
  • These inks were each applied to a 3.5 µ-thick polyethylene terephthalate (PET) film and dried to prepare a thermal transfer ink sheet.
  • The obtained thermal transfer ink sheet was evaluated as regards obtained prints by using a commercially available thermal transfer printer. The evaluation results are summarized in Table 1. It can be understood from the results that, with an increase in the amount of the carnauba wax slurry, a visocisty lowering effect was developed, whereby a thermally transferred image having a transfer rate and a resolution comparable to those of a wax ink was obtained while keeping the features of the resin, such as fastness.
  • Comparative Example 1
  • A thermally transferred image was obtained under the same conditions as those of Example 1 by using the ink ①.
  • The evaluation results as to obtained prints are shown in Table 1. In this case, since the ink has a very high viscosity, no sufficient transfer can be secured and hence a transferred image has a low coverage.
    Figure imgb0008
  • Example 2
  • Solution type inks each comprising as the main component a polyamide resin having a softening point of 86°C (melt viscosity at 120°C: 17,500 cps), a polystyrene­ acrylic resin having a softening point of 102°C (melt viscosity at 120°c: 50,000 cps), or a polystyrene resin having a softening point of 78°C (melt viscosity at 120°c: 11,000 cps) (in a 1/1 solvent mixture of toluene and methyl ethyl ketone) were admixed with 10, 20, 30, 40, and 50%, based on the resin, of a mixed slurry composed of polyethylene wax (melt viscosity at 120°C: 30 cps) and carnauba wax prepared at a ratio of 1:1 in the same manner as that of Example 1 to prepare inks.
  • Evaluation of the obtained prints was made in the same manner as that of Example 1. The results as shown in Table 2 were obtained. It was evidently recognized that addition of the slurry provided a viscosity lowering effect.
    Figure imgb0009
  • Example 3
  • A slurry of paraffin wax having a melting point of 105°C (melt viscosity at 120°C: 23 cps) in toluene was prepared. The same polyester resin as that described in Example 1 was admixed with 30%, based on the weight of the resin, of the slurry. The evaluation of the obtained prints was made in the same manner as that of Example 1 to obtain results as shown in Table 3.
  • As is apparent from Table 3, a sufficient viscosity lowering effect was developed and an ink having good performances in printing was obtained. Thus, it was found that even a high-melting wax having a melting point of higher than 100°C exhibited a viscosity lowering effect if the melt viscosity thereof was lowered.
  • Example 4
  • A polyamide resin having a softening point of 106°C (melt viscosity at 120°C: 120,000) was emulsified by the ordinary method to prepare an emulsion ink. Separately, a modified microcrystalline wax having a melting point of 87°C (melt viscosity at 120°C: 4 cps) was emulsified with a common emulsifier to prepare an emulsion. 20%, based on the weight of the resin, of the emulsion was added to the above-­ mentioned emulsion ink. Evaluation of the obtained prints was made in the same manner as that of Example 1 to obtain results as shown in Table 3.
  • As is apparent from Table 3, the emulsion ink having good performances in printing was prepared.
  • Comparative Example 2
  • The same resin ink as that used in Example 1 was admixed with 30%, based on the resin, of a polyester resin having a melting point of 78°C (melt viscosity at 120°C: 2,300 cps) to prepare an ink. Evaluation of the obtained prints was made in the same manner as that of Example 1 to obtain results as shown in Table 3.
  • As is apparent from Table 3, any viscosity lowering effect which will give good performances in printing could not be obtained though some decrease in viscosity was recognized. It was proved that a resin having a melt viscosity outside the scope of the present invention exhibited a remarkably low effect, even though it had a low melting point.
    Figure imgb0010

Claims (3)

1. An ink composition for the thermal transfer which comprises 100 parts by weight of a resin having a melt viscosity of 10,000 to 1,000,000 cps, measured at 120°c, and 5 to 250 parts by weight of a viscosity depressant having a melt viscosity of 1 to 600 cps, measured at 120°c, and being insoluble in a solvent to use or so partially soluble in the solvent that more than 1 gram of the viscosity depressant may not be soluble in 100 grams of the solvent at 40°c, said depressant being selected from a resin, a wax, a higher fatty acid, a higher alcohol and a synthetic ester compound.
2. An ink composition as claimed in Claim 1, which further comprises a solvent.
3. An ink composition as claimed in Claim 2, in which the insoluble portion of the depressant stands in the form of fine particles in the emulsion or the slurry.
EP19870116658 1986-11-19 1987-11-11 Thermal transfer ink Expired - Lifetime EP0268202B1 (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
JP27630586A JP2644999B2 (en) 1986-11-19 1986-11-19 Thermal transfer ink
JP276305/86 1986-11-19

Publications (3)

Publication Number Publication Date
EP0268202A2 true EP0268202A2 (en) 1988-05-25
EP0268202A3 EP0268202A3 (en) 1989-11-29
EP0268202B1 EP0268202B1 (en) 1993-06-09

Family

ID=17567599

Family Applications (1)

Application Number Title Priority Date Filing Date
EP19870116658 Expired - Lifetime EP0268202B1 (en) 1986-11-19 1987-11-11 Thermal transfer ink

Country Status (5)

Country Link
EP (1) EP0268202B1 (en)
JP (1) JP2644999B2 (en)
KR (1) KR920003247B1 (en)
DE (1) DE3786144T2 (en)
ES (1) ES2041254T3 (en)

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO1994025283A1 (en) * 1993-04-30 1994-11-10 E.I. Du Pont De Nemours And Company Laser-induced melt transfer process
EP0780240A3 (en) * 1995-12-18 1998-01-28 Ncr International Inc. Low energy thermal transfer formulation
US5757313A (en) * 1993-11-09 1998-05-26 Markem Corporation Lacer-induced transfer printing medium and method
FR2761927A1 (en) * 1997-04-11 1998-10-16 Ncr Int Inc SUPPORT FOR THERMAL TRANSFER

Families Citing this family (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2823124B2 (en) 1988-05-19 1998-11-11 フジコピアン株式会社 Thermal transfer ink
JP2567039B2 (en) * 1988-06-17 1996-12-25 キヤノン株式会社 Double recording method
JPH0238470A (en) * 1988-07-29 1990-02-07 Dainippon Printing Co Ltd Ink composition and its production
JPH0248628A (en) * 1988-08-11 1990-02-19 Toshiba Corp Endoscopic device

Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0126906A1 (en) * 1983-04-27 1984-12-05 RENKER GmbH & Co. KG Heat-sensitive registration/transfer material
JPS60115487A (en) * 1983-11-29 1985-06-21 Konishiroku Photo Ind Co Ltd Thermal transfer recording medium
JPS60178091A (en) * 1984-02-24 1985-09-12 Fujitsu Ltd Ink sheet for heat transfer recording
JPS60183195A (en) * 1984-02-29 1985-09-18 Fujitsu Ltd Thermal transfer recording sheet

Patent Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0126906A1 (en) * 1983-04-27 1984-12-05 RENKER GmbH & Co. KG Heat-sensitive registration/transfer material
JPS60115487A (en) * 1983-11-29 1985-06-21 Konishiroku Photo Ind Co Ltd Thermal transfer recording medium
JPS60178091A (en) * 1984-02-24 1985-09-12 Fujitsu Ltd Ink sheet for heat transfer recording
JPS60183195A (en) * 1984-02-29 1985-09-18 Fujitsu Ltd Thermal transfer recording sheet

Non-Patent Citations (4)

* Cited by examiner, † Cited by third party
Title
IEEE INTERNATIONAL ELECTRONIC MANUFACTURING TECHNOLOGY SYMPOSIUM, San Fransisco, CA, 15th-17th September 1986, pages 265-269, IEEE, New York, US; T. HARA et al.: "Reusable ribbon for thermal transfer printing" *
PATENT ABSTRACTS OF JAPAN, vol. 10, no. 18 (M-448)[2075], 24th January 1986; & JP-A-60 178 091 (FUJITSU K.K.) 12-09-1985 *
PATENT ABSTRACTS OF JAPAN, vol. 10, no. 25 (M-450)[2082], 31rd January 1986; & JP-A-60 183 195 (FUJITSU K.K.) 18-09-1985 *
PATENT ABSTRACTS OF JAPAN, vol. 9, no. 272 (M-425)[1995], 30th October 1985; & JP-A-60 115 487 (KONISHIROKU SHASHIN KOGYO K.K.) 21-06-1985 *

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO1994025283A1 (en) * 1993-04-30 1994-11-10 E.I. Du Pont De Nemours And Company Laser-induced melt transfer process
US5757313A (en) * 1993-11-09 1998-05-26 Markem Corporation Lacer-induced transfer printing medium and method
EP0780240A3 (en) * 1995-12-18 1998-01-28 Ncr International Inc. Low energy thermal transfer formulation
FR2761927A1 (en) * 1997-04-11 1998-10-16 Ncr Int Inc SUPPORT FOR THERMAL TRANSFER

Also Published As

Publication number Publication date
JPS63128992A (en) 1988-06-01
KR880006333A (en) 1988-07-22
JP2644999B2 (en) 1997-08-25
ES2041254T3 (en) 1993-11-16
DE3786144T2 (en) 1993-12-02
DE3786144D1 (en) 1993-07-15
KR920003247B1 (en) 1992-04-25
EP0268202A3 (en) 1989-11-29
EP0268202B1 (en) 1993-06-09

Similar Documents

Publication Publication Date Title
EP0207752B1 (en) Heat sensitive transferring recording medium
US5866637A (en) Magnetic thermal transfer ribbon with non-metallic magnets
EP0268202A2 (en) Thermal transfer ink
EP0235296B1 (en) Heat-sensitive melt-transfer recording medium
US5843579A (en) Magnetic thermal transfer ribbon with aqueous ferrofluids
US6057028A (en) Multilayered thermal transfer medium for high speed printing
JP3197826B2 (en) Thermal transfer recording medium
JP3090748B2 (en) Thermal transfer recording medium
JP2823124B2 (en) Thermal transfer ink
JP2716907B2 (en) Thermal transfer recording medium
US6231964B1 (en) Thermal transfer ribbons with large size wax or resin particles
US6171690B1 (en) Thermal transfer media with a mixture of non-melting solid particles of distinct sizes
US5866643A (en) High print quality thermal transfer ribbons
EP0830953B1 (en) Multilayered thermal transfer medium from water-based formulations
EP0631882A1 (en) Thermal transfer ink and thermal transfer element using the same
JPS63141786A (en) Manufacture of heat transfer ink dative film
JP3058993B2 (en) Thermal transfer ink sheet that can be used many times
JP2610873B2 (en) Transfer type thermal recording medium
JPH05185754A (en) Hot-melt transfer recording medium
JP2714512B2 (en) Thermal transfer recording medium
JP2002264527A (en) Heat transfer recording medium
JP2706893B2 (en) Thermal transfer recording medium
JP3090740B2 (en) Thermal transfer recording medium
JP2605068B2 (en) Thermal transfer recording medium
JP2744759B2 (en) Thermal transfer media

Legal Events

Date Code Title Description
PUAI Public reference made under article 153(3) epc to a published international application that has entered the european phase

Free format text: ORIGINAL CODE: 0009012

AK Designated contracting states

Kind code of ref document: A2

Designated state(s): DE ES FR GB IT NL

PUAL Search report despatched

Free format text: ORIGINAL CODE: 0009013

AK Designated contracting states

Kind code of ref document: A3

Designated state(s): DE ES FR GB IT NL

17P Request for examination filed

Effective date: 19891213

17Q First examination report despatched

Effective date: 19910718

GRAA (expected) grant

Free format text: ORIGINAL CODE: 0009210

AK Designated contracting states

Kind code of ref document: B1

Designated state(s): DE ES FR GB IT NL

REF Corresponds to:

Ref document number: 3786144

Country of ref document: DE

Date of ref document: 19930715

ET Fr: translation filed
ITF It: translation for a ep patent filed

Owner name: FUMERO BREVETTI S.N.C.

REG Reference to a national code

Ref country code: ES

Ref legal event code: FG2A

Ref document number: 2041254

Country of ref document: ES

Kind code of ref document: T3

PLBE No opposition filed within time limit

Free format text: ORIGINAL CODE: 0009261

STAA Information on the status of an ep patent application or granted ep patent

Free format text: STATUS: NO OPPOSITION FILED WITHIN TIME LIMIT

26N No opposition filed
PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: ES

Payment date: 19971128

Year of fee payment: 11

PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: NL

Payment date: 19971130

Year of fee payment: 11

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: ES

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 19981112

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: NL

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 19990601

NLV4 Nl: lapsed or anulled due to non-payment of the annual fee

Effective date: 19990601

REG Reference to a national code

Ref country code: GB

Ref legal event code: IF02

PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: GB

Payment date: 20021106

Year of fee payment: 16

PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: FR

Payment date: 20021108

Year of fee payment: 16

PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: DE

Payment date: 20021114

Year of fee payment: 16

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: GB

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 20031111

REG Reference to a national code

Ref country code: ES

Ref legal event code: FD2A

Effective date: 19991214

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: DE

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 20040602

GBPC Gb: european patent ceased through non-payment of renewal fee

Effective date: 20031111

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: FR

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 20040730

REG Reference to a national code

Ref country code: FR

Ref legal event code: ST

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: IT

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES;WARNING: LAPSES OF ITALIAN PATENTS WITH EFFECTIVE DATE BEFORE 2007 MAY HAVE OCCURRED AT ANY TIME BEFORE 2007. THE CORRECT EFFECTIVE DATE MAY BE DIFFERENT FROM THE ONE RECORDED.

Effective date: 20051111