US2279309A - Material for producing photographic multicolor images - Google Patents
Material for producing photographic multicolor images Download PDFInfo
- Publication number
- US2279309A US2279309A US282324A US28232439A US2279309A US 2279309 A US2279309 A US 2279309A US 282324 A US282324 A US 282324A US 28232439 A US28232439 A US 28232439A US 2279309 A US2279309 A US 2279309A
- Authority
- US
- United States
- Prior art keywords
- image
- dye
- dyes
- light
- images
- 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
- 239000000463 material Substances 0.000 title description 10
- 239000000975 dye Substances 0.000 description 39
- 238000000034 method Methods 0.000 description 10
- 239000002250 absorbent Substances 0.000 description 9
- 230000002745 absorbent Effects 0.000 description 9
- BQCADISMDOOEFD-UHFFFAOYSA-N Silver Chemical compound [Ag] BQCADISMDOOEFD-UHFFFAOYSA-N 0.000 description 7
- 238000004519 manufacturing process Methods 0.000 description 7
- 229910052709 silver Inorganic materials 0.000 description 7
- 239000004332 silver Substances 0.000 description 7
- 238000010521 absorption reaction Methods 0.000 description 4
- 238000004043 dyeing Methods 0.000 description 4
- 238000001429 visible spectrum Methods 0.000 description 4
- 108010010803 Gelatin Proteins 0.000 description 3
- 239000000980 acid dye Substances 0.000 description 3
- 229920000159 gelatin Polymers 0.000 description 3
- 239000008273 gelatin Substances 0.000 description 3
- 235000019322 gelatine Nutrition 0.000 description 3
- 235000011852 gelatine desserts Nutrition 0.000 description 3
- 230000003595 spectral effect Effects 0.000 description 3
- ANRHNWWPFJCPAZ-UHFFFAOYSA-M thionine Chemical compound [Cl-].C1=CC(N)=CC2=[S+]C3=CC(N)=CC=C3N=C21 ANRHNWWPFJCPAZ-UHFFFAOYSA-M 0.000 description 3
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Natural products CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 2
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 2
- 239000000981 basic dye Substances 0.000 description 2
- IOJUPLGTWVMSFF-UHFFFAOYSA-N benzothiazole Chemical compound C1=CC=C2SC=NC2=C1 IOJUPLGTWVMSFF-UHFFFAOYSA-N 0.000 description 2
- 230000008878 coupling Effects 0.000 description 2
- 238000010168 coupling process Methods 0.000 description 2
- 238000005859 coupling reaction Methods 0.000 description 2
- 229910052700 potassium Inorganic materials 0.000 description 2
- 239000011591 potassium Substances 0.000 description 2
- IOLCXVTUBQKXJR-UHFFFAOYSA-M potassium bromide Chemical compound [K+].[Br-] IOLCXVTUBQKXJR-UHFFFAOYSA-M 0.000 description 2
- OLSOUGWNONTDCK-UHFFFAOYSA-J tetrasodium 5-amino-3-[[4-[4-[(8-amino-1-hydroxy-3,6-disulfonatonaphthalen-2-yl)diazenyl]-3-methoxyphenyl]-2-methoxyphenyl]diazenyl]-4-hydroxynaphthalene-2,7-disulfonate Chemical compound [Na+].[Na+].[Na+].[Na+].C1=C(S([O-])(=O)=O)C=C2C=C(S([O-])(=O)=O)C(N=NC3=CC=C(C=C3OC)C=3C=C(C(=CC=3)N=NC=3C(=CC4=CC(=CC(N)=C4C=3O)S([O-])(=O)=O)S([O-])(=O)=O)OC)=C(O)C2=C1N OLSOUGWNONTDCK-UHFFFAOYSA-J 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- ATNOAWAQFYGAOY-UHFFFAOYSA-J Evans blue 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=C3C)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)C)=CC=C21 ATNOAWAQFYGAOY-UHFFFAOYSA-J 0.000 description 1
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 1
- SJEYSFABYSGQBG-UHFFFAOYSA-M Patent blue Chemical compound [Na+].C1=CC(N(CC)CC)=CC=C1C(C=1C(=CC(=CC=1)S([O-])(=O)=O)S([O-])(=O)=O)=C1C=CC(=[N+](CC)CC)C=C1 SJEYSFABYSGQBG-UHFFFAOYSA-M 0.000 description 1
- SMWDFEZZVXVKRB-UHFFFAOYSA-N Quinoline Chemical compound N1=CC=CC2=CC=CC=C21 SMWDFEZZVXVKRB-UHFFFAOYSA-N 0.000 description 1
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 1
- 229940037003 alum Drugs 0.000 description 1
- 239000000987 azo dye Substances 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 239000000298 carbocyanine Substances 0.000 description 1
- 230000006378 damage Effects 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- CHMBIJAOCISYEW-UHFFFAOYSA-N n-(4-aminophenyl)acetamide Chemical compound CC(=O)NC1=CC=C(N)C=C1 CHMBIJAOCISYEW-UHFFFAOYSA-N 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
- IWDCLRJOBJJRNH-UHFFFAOYSA-N p-cresol Chemical compound CC1=CC=C(O)C=C1 IWDCLRJOBJJRNH-UHFFFAOYSA-N 0.000 description 1
- 238000012797 qualification Methods 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 231100000489 sensitizer Toxicity 0.000 description 1
- ADZWSOLPGZMUMY-UHFFFAOYSA-M silver bromide Chemical compound [Ag]Br ADZWSOLPGZMUMY-UHFFFAOYSA-M 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 238000001228 spectrum Methods 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
- 239000001043 yellow dye Substances 0.000 description 1
Classifications
-
- G—PHYSICS
- G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
- G03C—PHOTOSENSITIVE MATERIALS FOR PHOTOGRAPHIC PURPOSES; PHOTOGRAPHIC PROCESSES, e.g. CINE, X-RAY, COLOUR, STEREO-PHOTOGRAPHIC PROCESSES; AUXILIARY PROCESSES IN PHOTOGRAPHY
- G03C7/00—Multicolour photographic processes or agents therefor; Regeneration of such processing agents; Photosensitive materials for multicolour processes
- G03C7/28—Silver dye bleach processes; Materials therefor; Preparing or processing such materials
Definitions
- Chromogen, Incorporated a corporation of Nevada No Drawing. Application June 30, 1939, Serial No. 282,324. In Germany-July 11, 1938 3 Claims.
- the present invention relates to a process for the manufacture of photographic materials.
- the dye for the production of photographic multi-color the image.
- the dye as is known, can be destroyed at the places where silver is present in the photographic image formed by developing and a positive dye-image is obtained in the taking material.
- a tanning ormordanting process and an image-like dyeing is used for the dyeing of the uppermost layer in most of the known processes.
- the present invention relates to an improvement of this known process for the purpose of producing master images.
- One object of the present invention is the production of multicolor master images the'part-images of which consist of dyes with widely separatedspectral absorption and which therefore permit the use of printing lights from widely separated spectral regions.
- Another object of the present invention is the processing of a taking material to a master-image from which the part-image in the uppermost layer can be printed with infra-red light, from which a second part-image can be printed with light from the extreme short-wave part of the visible spectrum or with ultra-violet light, and from which the third part-image can be printed with light lying between the other two printing lights and widely separated from at least one of them.
- the process of the present invention consists in the production of positive dye-images in the two pre-dyed layers of the taking material and converting the negative silver image originally produced in the uppermost layer into a positive dye-image; for the image in the uppermost layer a dye is used which absorbs infra-red light but is substantially transparent for visible light.
- a dye which absorbs infra-red light but is substantially transparent for visible light.
- the use of such dyes increases the qualification of the images so produced as master images. For printing there is required for each individual color-component-image a light which is of dverent color than the light necessary for printing the other component images, and the master images produced according to the process have the advantage that the printing lights can be chosen in part ranges of the spectrum lying far apart.
- light of wave lengths of 350 to 450 pp, 520 to 620 l and 780 to 800 up. may be used.
- the choice of such widely separated printing lights has the advantage that printing lights of those wave lengths which are not abso'rbedselectively by the dyes present in the master image but are absorbed by several of these dyes can be avoided.
- such dyes can be chosen whose absorption extends over a broader spectral range than is otherwise possible and therefore for the printing a broader spectral range can be used and better light yields are obtained.
- the process has the important advantage that the master images can be used for the printing onto multi-layer materials which contain an infra-red sensitive printing layer.
- the limits for the transparency and absorption of the dyes and the limits for the selectivity of the sensitisers in the printing material are greater than in the case of printing with light of wave length ranges which lie close together.
- Suitable infra-red absorbing dyes for the process are especially cyanine dyes. If the dyes are basic cyanine dyes then the procedure is such that the photographic layer ishardened or tanned at the places of the original silver negatives and the.
- the dye is subsequently used for dyeing the unhardened parts of the gelatin in which the dye penetrates its surface so that only one dye-image corresponding to the uppermost component image is formed.
- the dye can also be subsequently fixed in the layer in the known manner by means of salt formation or mordanting.
- acid dyes can be used which are capable of dyeing gelatin. It is also possible to bathe a weakly colored acid dye uniformly into the layer and to use it for the uniform fixing of a basic dye of good infra-red absorption and which in its unfixed state can be washed out from the layer.
- the uniformly dyed layer can be treated together with the other colored layers by means of the dye destroying solution whereby the acid dye is destroyed in accordance with the image and the basic dye can be washed out at these places.
- those dyes are preferably used which contain no salt-forming groups, 1. e. insoluble azo dyes, for example, the yellow dye obtainable by coupling diazotized p-acetylamino-aniline with p-kresol or the magenta dye obtainable by coupling diazotized u-naphthylamine with p-naphthol. Accordingly, a taking material can be used whose front layer is'colorat the place of the silver image.
- a taking material can be used whose front layer is'colorat the place of the silver image.
- a taking material can be used whose front layer is'colorat the place of the silver image.
- a taking material can be used whose front layer is'colorat the place of the silver image.
- a taking material can be
- the film is bathed for a few minutes in a bath of the following composition:
- the process can also be carried out in such proportional to the arate prints comprising three diiierently colored image records in superposition on a single support, one image record being formed of a dye predominately absorbent for light 01' a wave length shorter than 450 an. another image record being formed of a cyanine dye predominately absorbent for intra-red light but substantially transmittant for visible light, the third image record being formed of a dye which is absorbent for light rays oi the visible spectrum chiefly transmitted by both of the first mentioned dyes and which is substantially transmittant for light rays predominately absorbed 'by said first mentioned dyes.
- benzthiotricarbocyanines instead of the benzthiotricarbocyanines above referred .to pentacar-bocyanines can also be used and instead oi the benzthiazole dyes also the corresponding chinoline dyes or similar inira-red absorbing dyes can be used. v
- a master image for the production oi separate prints comprisingthree differently colored image records in superposition on a single support, one image record being formed of a dye predominantly absorbent for light of a wave- -20 length shorter than 450 another image record being formed or a dye predominantly absorbent for infra-red light but substantially transmittant for visible light, the third image record being formed oi a dye which is absorbent for light rays or the visible spectrum chiefly transmitted by both of the first mentioned dyes and which is substantially transmittant for light rays predominantly absorbed by said first mentioned dyes.
- a master image for the production of separate prints comprising three differently colored image records in superposition 'on a single support, one image record being formed of a dye predominantly absorbent for light of a wavelength shorter than 450 F11, another image record being formed oi a dye predominantly absorbent for light of a wave-length longer than 780 ms, both of said dyes being substantially transmittant for light rays having wave-lengths between 520 and 620 m the third image record 'being formed of a dye which is absorbent for light rays of the visible spectrum chiefly transmitted by both of the first mentioned dyes and which is substantially transmittant for light rays predominantly absorbed by said first mentioned dy s- BELA GASPAR.
Landscapes
- Physics & Mathematics (AREA)
- General Physics & Mathematics (AREA)
- Thermal Transfer Or Thermal Recording In General (AREA)
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE2279309X | 1938-07-11 |
Publications (1)
Publication Number | Publication Date |
---|---|
US2279309A true US2279309A (en) | 1942-04-14 |
Family
ID=7993502
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US282324A Expired - Lifetime US2279309A (en) | 1938-07-11 | 1939-06-30 | Material for producing photographic multicolor images |
Country Status (3)
Country | Link |
---|---|
US (1) | US2279309A (enrdf_load_stackoverflow) |
BE (1) | BE435120A (enrdf_load_stackoverflow) |
FR (1) | FR857660A (enrdf_load_stackoverflow) |
-
0
- BE BE435120D patent/BE435120A/xx unknown
-
1939
- 1939-06-30 US US282324A patent/US2279309A/en not_active Expired - Lifetime
- 1939-07-11 FR FR857660D patent/FR857660A/fr not_active Expired
Also Published As
Publication number | Publication date |
---|---|
BE435120A (enrdf_load_stackoverflow) | |
FR857660A (fr) | 1940-09-24 |
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