US3420732A - Transfer film and process of using same - Google Patents
Transfer film and process of using same Download PDFInfo
- Publication number
- US3420732A US3420732A US504055A US3420732DA US3420732A US 3420732 A US3420732 A US 3420732A US 504055 A US504055 A US 504055A US 3420732D A US3420732D A US 3420732DA US 3420732 A US3420732 A US 3420732A
- Authority
- US
- United States
- Prior art keywords
- polyamide
- retouchable
- electrophotographic
- layer
- 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
- 238000000034 method Methods 0.000 title description 8
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 claims description 70
- 239000004952 Polyamide Substances 0.000 claims description 38
- 229920002647 polyamide Polymers 0.000 claims description 38
- 239000000853 adhesive Substances 0.000 claims description 15
- 230000001070 adhesive effect Effects 0.000 claims description 15
- 239000010410 layer Substances 0.000 description 22
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 19
- 239000000243 solution Substances 0.000 description 10
- -1 nitrogen containing organic compounds Chemical class 0.000 description 9
- 239000011248 coating agent Substances 0.000 description 6
- 238000000576 coating method Methods 0.000 description 6
- 238000009877 rendering Methods 0.000 description 5
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 3
- 239000004743 Polypropylene Substances 0.000 description 3
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 3
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
- 238000010521 absorption reaction Methods 0.000 description 3
- 239000007864 aqueous solution Substances 0.000 description 3
- 230000003287 optical effect Effects 0.000 description 3
- 229920001155 polypropylene Polymers 0.000 description 3
- 108010010803 Gelatin Proteins 0.000 description 2
- 239000004698 Polyethylene Substances 0.000 description 2
- 230000004913 activation Effects 0.000 description 2
- 239000012790 adhesive layer Substances 0.000 description 2
- 230000015556 catabolic process Effects 0.000 description 2
- 238000010276 construction Methods 0.000 description 2
- 238000006731 degradation reaction Methods 0.000 description 2
- JBKVHLHDHHXQEQ-UHFFFAOYSA-N epsilon-caprolactam Chemical compound O=C1CCCCCN1 JBKVHLHDHHXQEQ-UHFFFAOYSA-N 0.000 description 2
- 239000008273 gelatin Substances 0.000 description 2
- 229920000159 gelatin Polymers 0.000 description 2
- 235000019322 gelatine Nutrition 0.000 description 2
- 235000011852 gelatine desserts Nutrition 0.000 description 2
- 238000003475 lamination Methods 0.000 description 2
- 238000002844 melting Methods 0.000 description 2
- 230000008018 melting Effects 0.000 description 2
- 229920000728 polyester Polymers 0.000 description 2
- 229920000573 polyethylene Polymers 0.000 description 2
- 239000004926 polymethyl methacrylate Substances 0.000 description 2
- 239000002904 solvent Substances 0.000 description 2
- UFFRSDWQMJYQNE-UHFFFAOYSA-N 6-azaniumylhexylazanium;hexanedioate Chemical compound [NH3+]CCCCCC[NH3+].[O-]C(=O)CCCCC([O-])=O UFFRSDWQMJYQNE-UHFFFAOYSA-N 0.000 description 1
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 1
- VVQNEPGJFQJSBK-UHFFFAOYSA-N Methyl methacrylate Chemical compound COC(=O)C(C)=C VVQNEPGJFQJSBK-UHFFFAOYSA-N 0.000 description 1
- 239000004677 Nylon Substances 0.000 description 1
- 229920002302 Nylon 6,6 Polymers 0.000 description 1
- 239000004820 Pressure-sensitive adhesive Substances 0.000 description 1
- XSTXAVWGXDQKEL-UHFFFAOYSA-N Trichloroethylene Chemical group ClC=C(Cl)Cl XSTXAVWGXDQKEL-UHFFFAOYSA-N 0.000 description 1
- 241001147416 Ursus maritimus Species 0.000 description 1
- 239000004957 Zytel Substances 0.000 description 1
- 229920006102 Zytel® Polymers 0.000 description 1
- 238000005299 abrasion Methods 0.000 description 1
- 239000003929 acidic solution Substances 0.000 description 1
- 150000001768 cations Chemical class 0.000 description 1
- BPHHNXJPFPEJOF-UHFFFAOYSA-J chembl296966 Chemical compound [Na+].[Na+].[Na+].[Na+].[O-]S(=O)(=O)C1=CC(S([O-])(=O)=O)=C(N)C2=C(O)C(N=NC3=CC=C(C=C3OC)C=3C=C(C(=CC=3)N=NC=3C(=C4C(N)=C(C=C(C4=CC=3)S([O-])(=O)=O)S([O-])(=O)=O)O)OC)=CC=C21 BPHHNXJPFPEJOF-UHFFFAOYSA-J 0.000 description 1
- 239000008119 colloidal silica Substances 0.000 description 1
- 239000003086 colorant Substances 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- YWJUZWOHLHBWQY-UHFFFAOYSA-N decanedioic acid;hexane-1,6-diamine Chemical compound NCCCCCCN.OC(=O)CCCCCCCCC(O)=O YWJUZWOHLHBWQY-UHFFFAOYSA-N 0.000 description 1
- 150000004985 diamines Chemical class 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 238000009472 formulation Methods 0.000 description 1
- 239000000499 gel Substances 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- GBMDVOWEEQVZKZ-UHFFFAOYSA-N methanol;hydrate Chemical compound O.OC GBMDVOWEEQVZKZ-UHFFFAOYSA-N 0.000 description 1
- 125000004184 methoxymethyl group Chemical group [H]C([H])([H])OC([H])([H])* 0.000 description 1
- 238000005065 mining Methods 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- JQZWHMOVSQRYRN-UHFFFAOYSA-M n-(2-chloroethyl)-n-ethyl-3-methyl-4-[2-(1,3,3-trimethylindol-1-ium-2-yl)ethenyl]aniline;chloride Chemical compound [Cl-].CC1=CC(N(CCCl)CC)=CC=C1C=CC1=[N+](C)C2=CC=CC=C2C1(C)C JQZWHMOVSQRYRN-UHFFFAOYSA-M 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- IJGRMHOSHXDMSA-UHFFFAOYSA-N nitrogen Substances N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 1
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 description 1
- 229920001778 nylon Polymers 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- 229920003229 poly(methyl methacrylate) Polymers 0.000 description 1
- 229920000139 polyethylene terephthalate Polymers 0.000 description 1
- 239000005020 polyethylene terephthalate Substances 0.000 description 1
- 229920002689 polyvinyl acetate Polymers 0.000 description 1
- 239000011118 polyvinyl acetate Substances 0.000 description 1
- 230000001681 protective effect Effects 0.000 description 1
- 230000005855 radiation Effects 0.000 description 1
- 230000033458 reproduction Effects 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 239000012748 slip agent Substances 0.000 description 1
- FTUYQIPAPWPHNC-UHFFFAOYSA-M sodium;4-[[4-[benzyl(ethyl)amino]phenyl]-[4-[benzyl(ethyl)azaniumylidene]cyclohexa-2,5-dien-1-ylidene]methyl]benzene-1,3-disulfonate Chemical compound [Na+].C=1C=C(C(=C2C=CC(C=C2)=[N+](CC)CC=2C=CC=CC=2)C=2C(=CC(=CC=2)S([O-])(=O)=O)S([O-])(=O)=O)C=CC=1N(CC)CC1=CC=CC=C1 FTUYQIPAPWPHNC-UHFFFAOYSA-M 0.000 description 1
- 239000004094 surface-active agent Substances 0.000 description 1
- UBOXGVDOUJQMTN-UHFFFAOYSA-N trichloroethylene Natural products ClCC(Cl)Cl UBOXGVDOUJQMTN-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- G—PHYSICS
- G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
- G03G—ELECTROGRAPHY; ELECTROPHOTOGRAPHY; MAGNETOGRAPHY
- G03G13/00—Electrographic processes using a charge pattern
- G03G13/22—Processes involving a combination of more than one step according to groups G03G13/02 - G03G13/20
-
- G—PHYSICS
- G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
- G03G—ELECTROGRAPHY; ELECTROPHOTOGRAPHY; MAGNETOGRAPHY
- G03G17/00—Electrographic processes using patterns other than charge patterns, e.g. an electric conductivity pattern; Processes involving a migration, e.g. photoelectrophoresis, photoelectrosolography; Processes involving a selective transfer, e.g. electrophoto-adhesive processes; Apparatus essentially involving a single such process
- G03G17/02—Electrographic processes using patterns other than charge patterns, e.g. an electric conductivity pattern; Processes involving a migration, e.g. photoelectrophoresis, photoelectrosolography; Processes involving a selective transfer, e.g. electrophoto-adhesive processes; Apparatus essentially involving a single such process with electrolytic development
-
- G—PHYSICS
- G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
- G03G—ELECTROGRAPHY; ELECTROPHOTOGRAPHY; MAGNETOGRAPHY
- G03G5/00—Recording members for original recording by exposure, e.g. to light, to heat, to electrons; Manufacture thereof; Selection of materials therefor
- G03G5/12—Recording members for multicolour processes
-
- G—PHYSICS
- G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
- G03G—ELECTROGRAPHY; ELECTROPHOTOGRAPHY; MAGNETOGRAPHY
- G03G8/00—Layers covering the final reproduction, e.g. for protecting, for writing thereon
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/14—Layer or component removable to expose adhesive
- Y10T428/1467—Coloring agent
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/28—Web or sheet containing structurally defined element or component and having an adhesive outermost layer
- Y10T428/2813—Heat or solvent activated or sealable
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/31504—Composite [nonstructural laminate]
- Y10T428/31725—Of polyamide
- Y10T428/31739—Nylon type
- Y10T428/31743—Next to addition polymer from unsaturated monomer[s]
- Y10T428/31746—Polymer of monoethylenically unsaturated hydrocarbon
Definitions
- This invention relates to an electrophotographic copysheet which can be retouched with water soluble dyestuffs. In one aspect this invention relates to color retouchable electrolytic electrophotographic full color prints. In another aspect this invention relates to a transfer film for providing a retouchable surface on an electrophotographic print.
- One electrophotographic method for providing full color reproductions of a light image utilizes electrolytic electrophotographic techniques. As described in US. 3,010,884 and 3,130,655 successive deposits of subtractive primary colors may be applied to the light exposed surface of an electrolytically developable photoconductive copysheet.
- Particularly suitable color developers include basic nitrogen containing organic compounds which are soluble in an aqueous acidic solution and which are insoluble in water at a pH above 7, as shown in US. 3,172,827.
- Another class of outstanding color developers are the water soluble oniurn cations which decompose electrolytically to form water insoluble compounds, as shown in US. 3,172,826.
- Another object of this invention is to provide a transfer film suitable for application to the surface of an electrophotographic print to provide a retouchable surface.
- a further object of this invention is to provide a method for rendering an electrophotographic print retouchable with water soluble dyestuffs.
- an electrophotographic copysheet having a visible image thereon can be rendered readily retouchable with water soluble dyestuffs without loss of other desirable physical properties if a layer of an essentially colorless methanol soluble synthetic polyamide is bonded to the image bearing copysheet surface.
- a preferred class of methanol soluble polyamides is the nitrogen substituted polyamides, particularly the N-alkoxymethyl polyamides, as described in US. 2,412,993, 2,430,860, 2,430,907 and 2,441,057.
- Other suitable methanol soluble synthetic polyamides include polyamides prepared with the use of certain diamines, e.g. triglycoldiamine, and multicomponent systems, e.g.
- methanol soluble polyamide a polyamide which can exist as at least a percent solution or gel in methanol at 25" C.
- the methanol soluble polyamides provide a retouchable surface for electrophotographic prints without the problems of curl and tackiness encountered in conventional prints. In the form of a retouchable layer having a thickness below about 5 mils they improve color saturation and appearance of the image and serve also to protect the print from abrasion, water spotting and degradation by actinic light.
- the retouchable layer may be prepared by coating the electrophotographic print with a methanol-water solution of the methanol soluble polyamide.
- a transfer film which comprises a transparent layer of methanol soluble polyamide on a releasable or strippable backing.
- Various backing materials with dry releasability from the polyamide may be used, such as a polypropylene film with or without a silica slip agent, polyethylene terephthalate, polypropylene coated paper, polyethylene coated paper, polyethylene film and poly-methyl methacrylate coated paper.
- a suitable essentially colorless adhesive system e.g.
- solvent and/or heat activatable adhesives and pressure sensitive adhesives can be employed.
- a heat activatable adhesive it should generally be capable of activation at a temperature below about C., preferably below 95 C., to avoid degradation of the print.
- the adhesive may be coated directly onto the print surface before application of the retouchable film or it may be carried on the surface of the retouchable film and form an integral component of the transfer film construction. Because of its relative ease in application the adhesive containing transfer film is preferred, generally with a releasable outer layer or liner to protect the adhesive prior to use if a pressure sensitive formulation is utilized.
- the surface of the retouchable film can be varied in texture from glossy to matte by selecting a release backing with the desired finish or by incorporating colloidal silica into the retouchable layer. Frequently it is desirable to include a surfactant into the retouchable layer or into the solution of retouching dyestutf to improve the rate and uniformitv of dye absorption.
- Example 1 A methanol soluble polyamide (B.C.I. nylon 819, N-methoxymethyl polyhexamethylene adipamide, 500- 600% ultimate elongation, 3400-3600 p.s.i. tensile strength, 12.4% water absorption, melting range 140- 148 C., tack point C.) was coated from the following solution onto a 5 mil polypropylene film to provide a dry filrn of one mil thickness.
- B.C.I. nylon 819 N-methoxymethyl polyhexamethylene adipamide, 500- 600% ultimate elongation, 3400-3600 p.s.i. tensile strength, 12.4% water absorption, melting range 140- 148 C., tack point C.
- Example 2 A polymethyl methacrylate coated paper was coated with the following solution to give a dry film thickness of one mil.
- a colorless polyester high strength adhesive (Du Pont 46950 polyester adhesive) was coated onto the po1yamide surface (dry coating thickness of one mil). The resulting construction was laminated by means of heated squeeze rolls at a temperature of about 80 C. to an electrophotographic print. After lamination the methylmethacrylate coated paper was stripped from the print leaving a surface with a pleasing semigloss texture.
- Example 3 A retouchable layer was prepared by coating an electrophotographic print with the following solution:
- a dimensionally stable, electrophotographic print having bonded to its image bearing surface an essentially colorless, methanol soluble, synthetic polyamide layer.
- an electrophotographic print which comprises an essentially colorless, methanol soluble, synthetic polyamide layer bonded to the surface of said print, said layer being retouchable with water soluble dyestuffs.
- a transfer film for rendering an electrophotographic print retouchable with water soluble dyestuffs which comprises an essentially colorless, methanol soluble, synthetic polyamide film releasably bonded to a support sheet.
- the process for rendering an electrophotographic print retouchable with water soluble dyestuffs which comprises (1) contacting the print surface with a transfer film comprising a layer of an essentially colorless, methanol soluble, synthetic polyamide releasably bonded to a support sheet, said support sheet being furthermost from said print surface, 2) bonding said polyamide layer to said print surface, and (3) removing said support sheet from said polyamide layer without breaking the bond between said print surface and said polyamide layer.
Landscapes
- Physics & Mathematics (AREA)
- General Physics & Mathematics (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Electrochemistry (AREA)
- Molecular Biology (AREA)
- Photoreceptors In Electrophotography (AREA)
- Printing Plates And Materials Therefor (AREA)
- Photosensitive Polymer And Photoresist Processing (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US50405565A | 1965-10-23 | 1965-10-23 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US3420732A true US3420732A (en) | 1969-01-07 |
Family
ID=24004671
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US504055A Expired - Lifetime US3420732A (en) | 1965-10-23 | 1965-10-23 | Transfer film and process of using same |
Country Status (4)
| Country | Link |
|---|---|
| US (1) | US3420732A (enExample) |
| BE (1) | BE688657A (enExample) |
| DE (1) | DE1522665B2 (enExample) |
| GB (1) | GB1144140A (enExample) |
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2018171873A1 (en) * | 2017-03-21 | 2018-09-27 | Hp Indigo B.V. | Liquid electrophotographic adhesive composition |
| CN114148109A (zh) * | 2021-11-09 | 2022-03-08 | 焦作卓立膜材料有限责任公司 | 一种可降解碳带及其制备方法 |
Citations (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3143416A (en) * | 1959-10-02 | 1964-08-04 | Azoplate Corp | Light sensitive coatings for screen printing comprising a light sensitive material with a condensate of a omega, omega'-diamine and a omega, omega'-dicarboxylic acid |
-
1965
- 1965-10-23 US US504055A patent/US3420732A/en not_active Expired - Lifetime
-
1966
- 1966-08-17 GB GB36918/66A patent/GB1144140A/en not_active Expired
- 1966-08-30 DE DE19661522665 patent/DE1522665B2/de active Pending
- 1966-10-21 BE BE688657D patent/BE688657A/xx unknown
Patent Citations (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3143416A (en) * | 1959-10-02 | 1964-08-04 | Azoplate Corp | Light sensitive coatings for screen printing comprising a light sensitive material with a condensate of a omega, omega'-diamine and a omega, omega'-dicarboxylic acid |
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2018171873A1 (en) * | 2017-03-21 | 2018-09-27 | Hp Indigo B.V. | Liquid electrophotographic adhesive composition |
| US10859937B2 (en) | 2017-03-21 | 2020-12-08 | Hp Indigo B.V. | Liquid electrophotographic adhesive composition |
| CN114148109A (zh) * | 2021-11-09 | 2022-03-08 | 焦作卓立膜材料有限责任公司 | 一种可降解碳带及其制备方法 |
Also Published As
| Publication number | Publication date |
|---|---|
| GB1144140A (en) | 1969-03-05 |
| DE1522665A1 (de) | 1969-10-16 |
| BE688657A (enExample) | 1967-04-21 |
| DE1522665B2 (de) | 1971-01-07 |
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