EP0653985B1 - Farbstoffgebende schicht für wärmeempfindliches farbstoffübertragungssystem - Google Patents
Farbstoffgebende schicht für wärmeempfindliches farbstoffübertragungssystem Download PDFInfo
- Publication number
- EP0653985B1 EP0653985B1 EP93918687A EP93918687A EP0653985B1 EP 0653985 B1 EP0653985 B1 EP 0653985B1 EP 93918687 A EP93918687 A EP 93918687A EP 93918687 A EP93918687 A EP 93918687A EP 0653985 B1 EP0653985 B1 EP 0653985B1
- Authority
- EP
- European Patent Office
- Prior art keywords
- film
- porous
- dye
- donor
- dyes
- 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.)
- Expired - Lifetime
Links
- 239000000975 dye Substances 0.000 claims abstract description 77
- 238000009792 diffusion process Methods 0.000 claims abstract description 20
- 239000011148 porous material Substances 0.000 claims abstract description 16
- 239000011230 binding agent Substances 0.000 claims abstract description 13
- -1 polyethylene Polymers 0.000 claims description 32
- 239000004743 Polypropylene Substances 0.000 claims description 23
- 229920001155 polypropylene Polymers 0.000 claims description 23
- 238000000034 method Methods 0.000 claims description 10
- 239000004698 Polyethylene Substances 0.000 claims description 8
- 229920000573 polyethylene Polymers 0.000 claims description 8
- 239000000463 material Substances 0.000 claims description 7
- 239000011241 protective layer Substances 0.000 claims description 6
- 238000010438 heat treatment Methods 0.000 claims description 3
- 230000008542 thermal sensitivity Effects 0.000 abstract description 6
- 239000010408 film Substances 0.000 description 94
- 239000010410 layer Substances 0.000 description 35
- 239000000243 solution Substances 0.000 description 26
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 18
- 230000000052 comparative effect Effects 0.000 description 15
- 230000003287 optical effect Effects 0.000 description 12
- 239000000203 mixture Substances 0.000 description 10
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 9
- 229920002799 BoPET Polymers 0.000 description 6
- 239000002904 solvent Substances 0.000 description 6
- 239000004372 Polyvinyl alcohol Substances 0.000 description 5
- 238000001035 drying Methods 0.000 description 5
- 229920000642 polymer Polymers 0.000 description 5
- 229920002451 polyvinyl alcohol Polymers 0.000 description 5
- 235000019422 polyvinyl alcohol Nutrition 0.000 description 5
- 239000000758 substrate Substances 0.000 description 5
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 4
- 229920000139 polyethylene terephthalate Polymers 0.000 description 4
- 239000005020 polyethylene terephthalate Substances 0.000 description 4
- 239000004800 polyvinyl chloride Substances 0.000 description 4
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
- 230000015572 biosynthetic process Effects 0.000 description 3
- 238000003475 lamination Methods 0.000 description 3
- 229920000915 polyvinyl chloride Polymers 0.000 description 3
- 238000002360 preparation method Methods 0.000 description 3
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
- 239000002981 blocking agent Substances 0.000 description 2
- 239000003795 chemical substances by application Substances 0.000 description 2
- 239000011248 coating agent Substances 0.000 description 2
- 238000000576 coating method Methods 0.000 description 2
- 238000011156 evaluation Methods 0.000 description 2
- 239000004519 grease Substances 0.000 description 2
- 238000003384 imaging method Methods 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 239000011259 mixed solution Substances 0.000 description 2
- 239000003960 organic solvent Substances 0.000 description 2
- 229920000515 polycarbonate Polymers 0.000 description 2
- 239000004417 polycarbonate Substances 0.000 description 2
- 229920000728 polyester Polymers 0.000 description 2
- 230000035945 sensitivity Effects 0.000 description 2
- 239000007787 solid Substances 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- 239000001043 yellow dye Substances 0.000 description 2
- 239000004952 Polyamide Substances 0.000 description 1
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 description 1
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 1
- BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 description 1
- 230000005540 biological transmission Effects 0.000 description 1
- 229920002301 cellulose acetate Polymers 0.000 description 1
- 238000010276 construction Methods 0.000 description 1
- 229920001577 copolymer Polymers 0.000 description 1
- 238000007598 dipping method Methods 0.000 description 1
- 230000002708 enhancing effect Effects 0.000 description 1
- 235000019441 ethanol Nutrition 0.000 description 1
- 230000004927 fusion Effects 0.000 description 1
- 230000009477 glass transition Effects 0.000 description 1
- 238000010030 laminating Methods 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- AJDUTMFFZHIJEM-UHFFFAOYSA-N n-(9,10-dioxoanthracen-1-yl)-4-[4-[[4-[4-[(9,10-dioxoanthracen-1-yl)carbamoyl]phenyl]phenyl]diazenyl]phenyl]benzamide Chemical compound O=C1C2=CC=CC=C2C(=O)C2=C1C=CC=C2NC(=O)C(C=C1)=CC=C1C(C=C1)=CC=C1N=NC(C=C1)=CC=C1C(C=C1)=CC=C1C(=O)NC1=CC=CC2=C1C(=O)C1=CC=CC=C1C2=O AJDUTMFFZHIJEM-UHFFFAOYSA-N 0.000 description 1
- MTZWHHIREPJPTG-UHFFFAOYSA-N phorone Chemical compound CC(C)=CC(=O)C=C(C)C MTZWHHIREPJPTG-UHFFFAOYSA-N 0.000 description 1
- 229920002647 polyamide Polymers 0.000 description 1
- 229920006289 polycarbonate film Polymers 0.000 description 1
- 239000011112 polyethylene naphthalate Substances 0.000 description 1
- 229920001721 polyimide Polymers 0.000 description 1
- 238000006116 polymerization reaction Methods 0.000 description 1
- 229920000036 polyvinylpyrrolidone Polymers 0.000 description 1
- 239000001267 polyvinylpyrrolidone Substances 0.000 description 1
- 235000013855 polyvinylpyrrolidone Nutrition 0.000 description 1
- 238000003825 pressing Methods 0.000 description 1
- 230000001681 protective effect Effects 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- 229910052710 silicon Inorganic materials 0.000 description 1
- 239000010703 silicon Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 239000010409 thin film Substances 0.000 description 1
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
- 229920002554 vinyl polymer Polymers 0.000 description 1
Images
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
- B41M5/382—Contact thermal transfer or sublimation processes
- B41M5/38278—Contact thermal transfer or sublimation processes using ink-containing structures, e.g. porous or microporous layers, alveoles or cellules
Definitions
- This invention relates to a binder-less porous donor for producing a dye diffusion thermal transfer image.
- a dye diffusion thermal transfer system is broadly used because it can produce an image in a completely dry process with a non-impact system using digitalized image information, the produced image having a high continuous gradation.
- image formation has hitherto been carried out by bringing a donor layer comprised of dyes and a macromolecular binder fixed on a donor substrate film in contact with a receptor layer on which an image is to be formed, bringing a thermal head into contact with the surface of the donor substrate film opposite the surface on which donor layer is placed, diffusing the dyes in the donor layer onto the receptor layer perpendicularly to the surface of the receptor layer by the thermal energy supplied from the thermal head, and then fixing the dyes thereon.
- This system is schematically illustrated in Fig. 1.
- Such systems are disclosed, for example, in Japanese Unexamined Patent Publication (Kokai) Nos. 3-13386, 3-65394, 3-65395, and 3-86589.
- a high affinity between the dyes and the binder is required in order to sufficiently diffuse the dyes in the donor layer. If the affinity is high, a high thermal energy is required for diffusing the dyes into the receptor layer. An energy threshold of diffusion of the dyes also exists. Thus, it is difficult to form an image having both a high continuous gradation and a high optical density at a low thermal energy.
- US 4 847 144 discloses a film suitable for producing a dye diffusion thermal transfer image comprising dyes localized in pores of a porous ink layer comprising a binder which is a thermofusible material solid at room temperature.
- the present invention provides a donor film that allows the dyes to be diffused at a low thermal energy, entails no energy threshold to the thermal diffusion of dyes, and is capable of forming an image having a high continuous gradation even in a wide optical density range.
- a donor layer is formed by physically locating diffusible dyes in the pores of a porous film having a pore size between 20 and 400 Gurley.
- the porous film of the present invention allows the dyes contained therein to be diffused onto the receptor layer at a low thermal energy without entailing any thermal threshold.
- the present invention provides a film for producing a dye diffusion thermal transfer image comprising diffusible dyes physically located in the pores of a porous film having a pore size between 20 and 400 Gurley and wherein the porous film contains no binder.
- the present invention further provides a process for the thermal diffusion transfer of a color image, comprising placing a color thermal diffusion dye donor sheet in intimate association with a receptor sheet, and heating said donor sheet in a desired pattern at a sufficient temperature (and pressure) to transfer the dyes from the donor sheet to the receptor sheet.
- the donor sheet comprises a porous polymeric material having a thermally diffusible dye located within the pores of the said porous material.
- the donor sheet contains no binder.
- Fig. 1 shows a construction of a general donor film and a comparative image forming system.
- Fig. 2 shows the lamination condition of the type 1 laminated film of this invention during the course of production.
- Fig. 3 shows one embodiment of the image forming system to which the donor film of this invention is applied.
- Fig. 4 shows another embodiment of the image forming system to which the donor film of this invention is applied.
- Fig. 5 shows a relation between burn time and the image density obtained in.Example 1.
- Fig. 6 shows a relation between burn time and the image density obtained in Comparative Example 1.
- Fig. 7 shows a relation between burn time and the image density obtained in Comparative Example 2.
- Fig. 8 shows a relation between burn time and the image density obtained in Example 2.
- Fig. 9 shows a relation between burn time and the image density obtained in Comparative Example 3.
- Fig. 10 shows a relation between burn time and the image density obtained in Comparative Example 4.
- Fig. 11 shows a relation between burn time and the image density obtained in Comparative Example 5.
- Fig. 12 shows a relation between burn time and the image density obtained in Comparative Example 6.
- Fig. 13 shows a relation between burn time and the image density obtained in Example 3.
- Fig. 14 shows a relation between burn time and the image density obtained in Example 4.
- Fig. 15 shows a relation between burn time and the image density obtained in Example 5.
- Fig. 16 shows a relation between burn time and the image density obtained in Example 6.
- Fig. 17 shows a relation between burn time and the image density obtained in Example 7.
- Fig. 18 shows a relation between burn time and the image density obtained in Example 8.
- Fig. 19 shows a relation between burn time and the image density obtained in Example 9.
- Fig. 20 shows a relation between burn time and the image density obtained in Example 10.
- Fig. 21 shows a relation between burn time and the image density obtained in Example 11.
- Fig. 22 shows a relation between burn time and the image density obtained in Example 12.
- the porous films which can be used in this invention include, for example, films made out of polyethylene, polypropylene, polyester, and polycarbonate, and thin paper.
- the film thickness is in the range of 10 ⁇ m to 25 ⁇ m, preferably 14 ⁇ m to 20 ⁇ m.
- the pore size expressed in a Gurley value is in the range of 20-400.
- Typical examples of the porous films which can be used are Polyethylene film #06106-5, Polypropylene film 17770-28, Polypropylene film #77O-2S, Polypropylene film #77O-3S, Polypropylene film #77O-4S, Polypropylene film #77O-6S, Polypropylene film #739-2B (all produced by 3M Company), and the like.
- the pore size of the porous film is between 20 and 400 Gurley. If this value is more than 400, it becomes difficult to introduce dyes into the pores. If this value is less than 20, the resolution of the image is lowered.
- cyan dyes, magenta dyes, yellow dyes, and any other conventional dyes can be used.
- these dyes may be dissolved in an appropriate solvent such as an organic solvent, e.g. tetrahydrofuran, methylethylketone, or ethyl alcohol, the solution being applied on one or both sides of the film by any conventional means, such as a Meyer barTM or a knife coater.
- the porous film may be immersed in a dye solution. Subsequent drying for the removal of the solvent accomplishes the formation of the donor layer. Since the solvent does not contain a binder, the dyes are not accompanied by a binder.
- the overall concentration of dyes in the above-mentioned dye solution depends on the type of dye, but is generally in the range of 1-10% by weight, preferably 2-7% by weight.
- a protective layer is placed on the surface of the above-mentioned porous film opposite the surface on which the donor layer is placed (in the case where the donor-layer is formed on only one of the surfaces of the porous film).
- the protective layer may be very thin, and have a thickness in the range of 1 ⁇ m to 10 ⁇ m, preferably 1 ⁇ m to 3 ⁇ m.
- the protective layer serves to prevent thermal influences from the thermal head, i.e., to prevent the thermal fusion of the porous film, and can be formed by applying a solution of polymer having a high glass transition temperature on the surface of the porous film opposite the surface having the donor layer placed thereon, followed by drying.
- the polymers that can be used for this purpose are polyvinyl alcohol, polyvinylpyrrolidone, and the like. Any solvent can be used for this purpose as long as it can dissolve the polymer to be used. For example, water, a mixture of water with a hydrophilic organic solvent, or the like can be used.
- the concentration of the polymer in the solvent is 1-10% by weight, preferably 3-5% by weight.
- the protective layer may also be formed by laminating a thin film on the porous film.
- a polyethylene terephthalate (PET) film, a polyethylene naphthalate (PEN) film, a polyimide film, a polyamide film, a polycarbonate film, or the like can be used.
- the receptor film which can be applied to the donor film of this invention is comprised of a substrate film and a receptor layer formed on the surface thereof.
- the receptor layer is, for example, comprised of a layer of polyvinyl chloride, a copolymer of vinyl chloride and vinyl acetate, polyester, polycarbonate, etc.
- the receptor layer can be formed by dissolving one of these materials in an appropriate solvent, and then applying the solution on the substrate film, followed by drying. Any conventional substrate film can be used.
- the porous donor film of the present invention allows the diffusion of dyes to be carried out at a low thermal energy.
- an image with a high continuous gradation, even in the case of a low optical density, can be formed.
- the service life of the thermal head can be extended.
- Dye mixtures were prepared by dissolving the following dyes in tetrahydrofuran (THF) and then mixing them, respectively. Each concentration of the dye was adjusted to 5% by weight. Each of the dye formulas are set forth below.
- Table 1 Material Tm (°C) Thickness ( ⁇ m) Gurley (s/50cm 3 cc air) Polyethylene film #06101-5 124-131 14 19 Polypropylene film #770-28 163-167 20 10 Polypropylene film #770-2S 159-163 25 400 Polypropylene film #770-3S 158-163 17 240 Polypropylene film #770-4S 158-162 15 400 Polypropylene film #770-6S 155-160 10 - Polypropylene film #739-2B 158-162 20 34 Paper - 22 -
- Porous polyethylene film #0610-5 (from 3M, U.S.A) was placed on a paper, and a solution of dye mixture in THF was coated on the film using a #lO Meyer barTM. After being dried at 65°C for 20 minutes, an aqueous 5% by weight solution of polyvinyl alcohol having a polymerization degree of 2000 was coated on the surface which was not dye-coated using a #lO Meyer barTM, and dried again under the same conditions.
- a porous donor film using porous polyethylene film #O6lO-5 (from 3M, U.S.A) was prepared in the same manner as that in type 1.
- a 3.5 ⁇ m thick PET film was laminated thereon instead of coating it with polyvinyl alcohol.
- the lamination was carried out using a laminator produced by Gunma Ushio at 110°C at a speed of 9.5 mm/s.
- the film lamination process is shown in Fig. 2.
- a porous polyethylene film #06101-5 (from 3M, U.S.A) was placed on a 3.5 ⁇ m thick PET film, and a dye mixture in THF was coated on the surface thereof using a #lO Meyer barTM. It was then dried at 65°C for 20 minutes.
- a porous polyethylene film #06101-5 (from 3M, U.S.A) was dipped in a solution of magenta dye mixture in THF. After dried at 65°C for 20 minutes, the 3.5 mm thick PET film was laminated on a surface thereof as mentioned under type 2.
- Porous polypropylene films (#770-28, #77O-2S, #77O-3S, #77O-4S, #77O-6S, and #739-2B, all from 3M, U.S.A) were prepared in the same manner as that in type 1.
- a porous polypropylene film #77O-2S was prepared in the same manner as that in type 1, but the film did not have the PVOH film layer. Furthermore, when printing, neither an anti-stick agent nor a slipping agent for the thermal head was used.
- a donor film was prepared by using thin paper, and it was evaluated.
- a polyvinyl chloride (PVC) resin from Mitsubishi Kasei Vinyl was dissolved in tetrahydrofuran (THF) to prepare a 5% weight PVC solution.
- a solution of an anti-blocking agent (5% by weight of FC430TM, from 3M, U.S.A., in THF) was prepared.
- the mixed solution prepared therefrom (10 g of the PVC solution + 0.5 g of the FC430TM solution) was coated on the surface of a 4 mil (0.1mm) thick polyethyleneterephthalate (PET) film using a #2O Meyer barTM. After being dried at 65°C for 20 minutes, this film was used as a receptor film.
- FIG. 1 A thermal printer having a 200 dpi (500 dots per cm), 13.4 cm width thermal head (from 3M, U.S.A.) was employed to carry out printing evaluations. For applying pressure, a 1.95 kg weight was placed on the thermal head.
- Fig. 1, Fig. 3 and Fig. 4 schematically show the various imaging configurations used to carry out the examples and comparative examples set forth below. Figs 3 and 4 are in accordance with the present invention. The imaging process was carried out in eight steps by varying the voltage applied to the thermal head. The burn times and thermal energies are shown in the following table 2.
- a densitometer (Macbeth TR924TM, from Macbeth Process Measurement, U.S.A.) was utilized. A type filters were used.
- the porous donor films (type 1) were tested using a thermal printer at an applied voltage of 11.5 volts, and a linear image gradation was attained. The result is shown in Fig. 5. When more than 11.5 volts was applied, the donor films were partially melted by the heat. These donor films did not stick nor did they cause transfer of the dye mixture to the receptor layer upon the application of pressure only.
- ink ribbon having different dyes (cyan, magenta, and yellow) were produced.
- dye solutions comprised of dyes, cellulose acetate, an anti-blocking agent and MEK were coated on the surface of a 6 ⁇ m thick PET film using a #10 Meyer barTM, and then dried at 60°C for 10 minutes in an oven.
- an ink ribbon which is a donor layer of 5 nm thickness was evaluated in the same manner as that of Example 1. They showed a low sensitivity to the applied thermal energy in comparison with those of the donor films (type 1). The result is shown in Fig. 6. As illustrated, they required higher energies for dye diffusion in comparison with type 1 films.
- the magenta ink ribbon carried out the transfer of the color material to the receptor by the application of pressure only.
- type 2 donor films were chosen.
- the printing conditions were the same as those of Example 1, except for applied voltage, the voltage being increased from 11.4 volts to 14.0 volts.
- the optical densities of the printed images are clearly in a good linear relation to the thermal energy applied from the thermal head as in Example 1. The results are shown in Fig. B.
- Fig. 9 Three types of ink ribbons as shown in Fig. l were prepared using the same dyes and examined in the same manner as in Example 2. The result is shown in Fig. 9.
- the magenta ink ribbon showed a better thermal sensitivity than the others, but the dye transfer to the receptor layer because of pressure was shown and, thus, the Dmin was raised.
- the cyan ink ribbon was sticking to the receptor layer at the 7th or more level. Their total thermal sensitivities were lower than that of type 2 donor film.
- Example 12 Three commercially available ink ribbons (from C company) were examined in the same manner as in Example 2. The result is shown in Fig. 12. They also had low thermal sensitivities, and covered a narrow image density range.
- Porous donor films (type 3) were prepared to increase the range between Dmax and Dmin of the image production.
- the printing conditions were the same as those of Example 2.
- Their optical densities are in a linear relation to the applied thermal energy.
- the energy requirement for the cyan image was 5.1 Joule/cm 2 and those for the magenta and yellow images were 5.9 Joule/cm 2 .
- the result is shown in Fig. 13. These values are quite a bit smaller than those of the commercially available type donor films.
- Porous donor films (type 4) were examined in the same manner as that in Example 2. The image gradation was also observed. The result is shown in Fig. 14. From this example, it can be considered that there is no need for a special coater for producing the donor films. Only the process of dipping the porous film into the dye solution is required.
- Porous polypropylene film (type 5, #770-28, from 3M, U.S.A.) was evaluated in the same manner as that in Example 1, except that the applied voltage was increased to 17.0 volts. As a result, it was found that the optical densities on a receptor layer were in linear relation to the applied thermal energy during the printing. The result is shown in Fig. 15.
- Porous polypropylene films (type 5, #77O-2S, from 3M, U.S.A.), were evaluated in the same manner as that in Example 5. The result demonstrates that the optical densities of the printed images on a receptor layer showed gradation. Furthermore, they were changed in linear relation to the applied thermal energy. The result is shown in Fig. 16.
- Type 7 magenta dye-coated thin papers were evaluated in the same manner as that in Example 5. The results are shown in Fig. 22, demonstrating that a film not entailing deformation, shrinkage, or melting of minute pores due to the heat application can also be used as a donor containing no binder.
Landscapes
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Physics & Mathematics (AREA)
- Optics & Photonics (AREA)
- Thermal Transfer Or Thermal Recording In General (AREA)
Claims (5)
- Film zur Herstellung eines Thermo-Farbdiffusions-Wärmeübertragungsbildes mit thermisch diffundierbaren Farben, die physisch in Poren eines porösen Films angeordnet sind, dadurch gekennzeichnet, daß der Gurley-Wert des porösen Films zwischen 20 und 400 Sekunden pro 50 Kubikzentimeter Luft beträgt, wobei der poröse Film kein Bindemittel enthält.
- Film nach Anspruch 1, bei dem der poröse Film ein poröser Polyethylenfilm oder ein poröser Polypropylenfilm ist.
- Film nach Anspruch 1 oder 2, bei dem eine Schutzschicht auf eine Fläche des porösen Films aufgebracht oder laminiert ist.
- Verfahren zur Thermodiffusionsübertragung eines Farbbildes, mit den Schritten des Anordnens einer Farb-Thermodiffusions-Farbstoffgeberbahn in enger Verbindung mit einer Rezeptorbahn und des Enwärmens der Farbstoffgeberbahn nach einem gewünschten Muster mit einer für die Übertragung der Farben von der Farbstoffgeberbahn auf die Rezeptorbahn ausreichenden Temperatur, wobei das Verfahren dadurch gekennzeichnet ist, daß die Farbstoffgeberbahn ein poröses polymeres Material nach einem der Ansprüche 1 bis 3 aufweist.
- Verfahren zur Thermodiffusionsübertragung eines Farbbildes, mit den Schritten des Anordnens einer Farb-Thermodiffusions-Farbstoffgeberbahn in enger Verbindung mit einer Rezeptorbahn und des Erwärmens der Farbstoffgeberbahn nach einem gewünschten Muster mit einer für die Übertragung der Farben von der Farbstoffgeberbahn auf die Rezeptorbahn ausreichenden Temperatur und einem solchen Druck, wobei das Verfahren dadurch gekennzeichnet ist, daß die Farbstoffgeberbahn ein poröses polymeres Material nach einem der Ansprüche 1 bis 3 aufweist
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP4210307A JPH0699668A (ja) | 1992-08-06 | 1992-08-06 | 染料拡散型熱転写画像作製用バインダーレス多孔性ドナーフィルム |
JP210307/92 | 1992-08-06 | ||
PCT/US1993/007418 WO1994003334A1 (en) | 1992-08-06 | 1993-08-06 | Dye-donor film for thermosensitive dye-transfer system |
Publications (2)
Publication Number | Publication Date |
---|---|
EP0653985A1 EP0653985A1 (de) | 1995-05-24 |
EP0653985B1 true EP0653985B1 (de) | 1996-10-09 |
Family
ID=16587246
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
EP93918687A Expired - Lifetime EP0653985B1 (de) | 1992-08-06 | 1993-08-06 | Farbstoffgebende schicht für wärmeempfindliches farbstoffübertragungssystem |
Country Status (4)
Country | Link |
---|---|
EP (1) | EP0653985B1 (de) |
JP (1) | JPH0699668A (de) |
DE (1) | DE69305354T2 (de) |
WO (1) | WO1994003334A1 (de) |
Families Citing this family (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
IL135736A (en) | 2000-04-18 | 2004-07-25 | Polysack Plastic Ind R A C S L | Net for protecting plants from light |
Family Cites Families (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4784905A (en) * | 1985-03-01 | 1988-11-15 | Ricoh Company, Ltd. | Thermosensitive image transfer recording medium |
JPS63246281A (ja) * | 1986-11-01 | 1988-10-13 | Ricoh Co Ltd | 転写記録媒体 |
-
1992
- 1992-08-06 JP JP4210307A patent/JPH0699668A/ja active Pending
-
1993
- 1993-08-06 DE DE69305354T patent/DE69305354T2/de not_active Expired - Fee Related
- 1993-08-06 WO PCT/US1993/007418 patent/WO1994003334A1/en active IP Right Grant
- 1993-08-06 EP EP93918687A patent/EP0653985B1/de not_active Expired - Lifetime
Also Published As
Publication number | Publication date |
---|---|
WO1994003334A1 (en) | 1994-02-17 |
DE69305354D1 (de) | 1996-11-14 |
EP0653985A1 (de) | 1995-05-24 |
DE69305354T2 (de) | 1997-05-15 |
JPH0699668A (ja) | 1994-04-12 |
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