US3015562A - Receiving sheet for use in photographic silver transfer process - Google Patents
Receiving sheet for use in photographic silver transfer process Download PDFInfo
- Publication number
- US3015562A US3015562A US733505A US73350558A US3015562A US 3015562 A US3015562 A US 3015562A US 733505 A US733505 A US 733505A US 73350558 A US73350558 A US 73350558A US 3015562 A US3015562 A US 3015562A
- Authority
- US
- United States
- Prior art keywords
- silver halide
- transfer process
- image
- silver
- maleic anhydride
- 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
- 239000004332 silver Substances 0.000 title claims description 26
- 229910052709 silver Inorganic materials 0.000 title claims description 26
- 238000000034 method Methods 0.000 title claims description 16
- BQCADISMDOOEFD-UHFFFAOYSA-N Silver Chemical compound [Ag] BQCADISMDOOEFD-UHFFFAOYSA-N 0.000 title description 6
- 239000000463 material Substances 0.000 claims description 28
- -1 SILVER HALIDE Chemical class 0.000 claims description 24
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 16
- 239000003795 chemical substances by application Substances 0.000 claims description 15
- 229920001577 copolymer Polymers 0.000 claims description 11
- 230000002209 hydrophobic effect Effects 0.000 claims description 9
- 239000000203 mixture Substances 0.000 claims description 9
- 229920005989 resin Polymers 0.000 claims description 8
- 239000011347 resin Substances 0.000 claims description 8
- GGCZERPQGJTIQP-UHFFFAOYSA-N sodium;9,10-dioxoanthracene-2-sulfonic acid Chemical compound [Na+].C1=CC=C2C(=O)C3=CC(S(=O)(=O)O)=CC=C3C(=O)C2=C1 GGCZERPQGJTIQP-UHFFFAOYSA-N 0.000 claims description 7
- 230000003287 optical effect Effects 0.000 claims description 4
- 230000001131 transforming effect Effects 0.000 claims description 2
- 239000011888 foil Substances 0.000 description 16
- 238000000576 coating method Methods 0.000 description 12
- 239000011248 coating agent Substances 0.000 description 11
- 229920002554 vinyl polymer Polymers 0.000 description 9
- 239000002585 base Substances 0.000 description 8
- 229920002301 cellulose acetate Polymers 0.000 description 8
- QIGBRXMKCJKVMJ-UHFFFAOYSA-N Hydroquinone Chemical compound OC1=CC=C(O)C=C1 QIGBRXMKCJKVMJ-UHFFFAOYSA-N 0.000 description 6
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 6
- SQGYOTSLMSWVJD-UHFFFAOYSA-N silver(1+) nitrate Chemical compound [Ag+].[O-]N(=O)=O SQGYOTSLMSWVJD-UHFFFAOYSA-N 0.000 description 6
- 239000002904 solvent Substances 0.000 description 5
- 239000002253 acid Substances 0.000 description 4
- 125000004433 nitrogen atom Chemical group N* 0.000 description 4
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
- 108010010803 Gelatin Proteins 0.000 description 3
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- 239000003513 alkali Substances 0.000 description 3
- 150000001450 anions Chemical class 0.000 description 3
- 230000018109 developmental process Effects 0.000 description 3
- 238000001035 drying Methods 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
- FPYJFEHAWHCUMM-UHFFFAOYSA-N maleic anhydride Chemical compound O=C1OC(=O)C=C1 FPYJFEHAWHCUMM-UHFFFAOYSA-N 0.000 description 3
- 229910052757 nitrogen Inorganic materials 0.000 description 3
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 description 3
- 229920003023 plastic Polymers 0.000 description 3
- 229910001961 silver nitrate Inorganic materials 0.000 description 3
- UZKWTJUDCOPSNM-UHFFFAOYSA-N 1-ethenoxybutane Chemical compound CCCCOC=C UZKWTJUDCOPSNM-UHFFFAOYSA-N 0.000 description 2
- HZAXFHJVJLSVMW-UHFFFAOYSA-N 2-Aminoethan-1-ol Chemical compound NCCO HZAXFHJVJLSVMW-UHFFFAOYSA-N 0.000 description 2
- XLLIQLLCWZCATF-UHFFFAOYSA-N 2-methoxyethyl acetate Chemical compound COCCOC(C)=O XLLIQLLCWZCATF-UHFFFAOYSA-N 0.000 description 2
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 2
- PAYRUJLWNCNPSJ-UHFFFAOYSA-N Aniline Chemical compound NC1=CC=CC=C1 PAYRUJLWNCNPSJ-UHFFFAOYSA-N 0.000 description 2
- 229920002284 Cellulose triacetate Polymers 0.000 description 2
- QCZAWDGAVJMPTA-RNFRBKRXSA-N ClC1=CC=CC(=N1)C1=NC(=NC(=N1)N[C@@H](C(F)(F)F)C)N[C@@H](C(F)(F)F)C Chemical compound ClC1=CC=CC(=N1)C1=NC(=NC(=N1)N[C@@H](C(F)(F)F)C)N[C@@H](C(F)(F)F)C QCZAWDGAVJMPTA-RNFRBKRXSA-N 0.000 description 2
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 2
- NNLVGZFZQQXQNW-ADJNRHBOSA-N [(2r,3r,4s,5r,6s)-4,5-diacetyloxy-3-[(2s,3r,4s,5r,6r)-3,4,5-triacetyloxy-6-(acetyloxymethyl)oxan-2-yl]oxy-6-[(2r,3r,4s,5r,6s)-4,5,6-triacetyloxy-2-(acetyloxymethyl)oxan-3-yl]oxyoxan-2-yl]methyl acetate Chemical compound O([C@@H]1O[C@@H]([C@H]([C@H](OC(C)=O)[C@H]1OC(C)=O)O[C@H]1[C@@H]([C@@H](OC(C)=O)[C@H](OC(C)=O)[C@@H](COC(C)=O)O1)OC(C)=O)COC(=O)C)[C@@H]1[C@@H](COC(C)=O)O[C@@H](OC(C)=O)[C@H](OC(C)=O)[C@H]1OC(C)=O NNLVGZFZQQXQNW-ADJNRHBOSA-N 0.000 description 2
- 150000008064 anhydrides Chemical class 0.000 description 2
- 239000011324 bead Substances 0.000 description 2
- JHIVVAPYMSGYDF-UHFFFAOYSA-N cyclohexanone Chemical compound O=C1CCCCC1 JHIVVAPYMSGYDF-UHFFFAOYSA-N 0.000 description 2
- 238000009792 diffusion process Methods 0.000 description 2
- 238000002845 discoloration Methods 0.000 description 2
- DQJJMWZRDSGUJP-UHFFFAOYSA-N ethenoxyethene;furan-2,5-dione Chemical compound C=COC=C.O=C1OC(=O)C=C1 DQJJMWZRDSGUJP-UHFFFAOYSA-N 0.000 description 2
- 229920001600 hydrophobic polymer Polymers 0.000 description 2
- 125000001570 methylene group Chemical group [H]C([H])([*:1])[*:2] 0.000 description 2
- 230000006911 nucleation Effects 0.000 description 2
- 238000010899 nucleation Methods 0.000 description 2
- 239000003960 organic solvent Substances 0.000 description 2
- 239000004033 plastic Substances 0.000 description 2
- 229920002037 poly(vinyl butyral) polymer Polymers 0.000 description 2
- IOLCXVTUBQKXJR-UHFFFAOYSA-M potassium bromide Chemical compound [K+].[Br-] IOLCXVTUBQKXJR-UHFFFAOYSA-M 0.000 description 2
- 230000033458 reproduction Effects 0.000 description 2
- GEHJYWRUCIMESM-UHFFFAOYSA-L sodium sulfite Chemical compound [Na+].[Na+].[O-]S([O-])=O GEHJYWRUCIMESM-UHFFFAOYSA-L 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- 238000011282 treatment Methods 0.000 description 2
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 1
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 description 1
- JMOGPBKCUKFZIE-UHFFFAOYSA-N C1(C=C/C(=O)O1)=O.C(C(C)C)OCC(C)C Chemical compound C1(C=C/C(=O)O1)=O.C(C(C)C)OCC(C)C JMOGPBKCUKFZIE-UHFFFAOYSA-N 0.000 description 1
- 229920008347 Cellulose acetate propionate Polymers 0.000 description 1
- DQEFEBPAPFSJLV-UHFFFAOYSA-N Cellulose propionate Chemical compound CCC(=O)OCC1OC(OC(=O)CC)C(OC(=O)CC)C(OC(=O)CC)C1OC1C(OC(=O)CC)C(OC(=O)CC)C(OC(=O)CC)C(COC(=O)CC)O1 DQEFEBPAPFSJLV-UHFFFAOYSA-N 0.000 description 1
- GRYLNZFGIOXLOG-UHFFFAOYSA-N Nitric acid Chemical compound O[N+]([O-])=O GRYLNZFGIOXLOG-UHFFFAOYSA-N 0.000 description 1
- 229920002319 Poly(methyl acrylate) Polymers 0.000 description 1
- 239000004793 Polystyrene Substances 0.000 description 1
- FOIXSVOLVBLSDH-UHFFFAOYSA-N Silver ion Chemical compound [Ag+] FOIXSVOLVBLSDH-UHFFFAOYSA-N 0.000 description 1
- QYKIQEUNHZKYBP-UHFFFAOYSA-N Vinyl ether Chemical compound C=COC=C QYKIQEUNHZKYBP-UHFFFAOYSA-N 0.000 description 1
- 150000001241 acetals Chemical class 0.000 description 1
- 230000032683 aging Effects 0.000 description 1
- 125000000217 alkyl group Chemical group 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 238000004061 bleaching Methods 0.000 description 1
- 125000004432 carbon atom Chemical group C* 0.000 description 1
- 229920006217 cellulose acetate butyrate Polymers 0.000 description 1
- 229920001727 cellulose butyrate Polymers 0.000 description 1
- 229920006218 cellulose propionate Polymers 0.000 description 1
- 235000015165 citric acid Nutrition 0.000 description 1
- KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid group Chemical class C(CC(O)(C(=O)O)CC(=O)O)(=O)O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 description 1
- 230000007547 defect Effects 0.000 description 1
- 239000000839 emulsion Substances 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- DDSRCCOGHFIQDX-UHFFFAOYSA-N furan-2,5-dione;methoxymethane Chemical compound COC.O=C1OC(=O)C=C1 DDSRCCOGHFIQDX-UHFFFAOYSA-N 0.000 description 1
- 150000004820 halides Chemical class 0.000 description 1
- 125000000623 heterocyclic group Chemical group 0.000 description 1
- 230000007062 hydrolysis Effects 0.000 description 1
- 238000006460 hydrolysis reaction Methods 0.000 description 1
- 230000003301 hydrolyzing effect Effects 0.000 description 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
- 229910052500 inorganic mineral Inorganic materials 0.000 description 1
- XJRBAMWJDBPFIM-UHFFFAOYSA-N methyl vinyl ether Chemical compound COC=C XJRBAMWJDBPFIM-UHFFFAOYSA-N 0.000 description 1
- 239000011707 mineral Substances 0.000 description 1
- 229910017604 nitric acid Inorganic materials 0.000 description 1
- CMCWWLVWPDLCRM-UHFFFAOYSA-N phenidone Chemical compound N1C(=O)CCN1C1=CC=CC=C1 CMCWWLVWPDLCRM-UHFFFAOYSA-N 0.000 description 1
- 229920002959 polymer blend Polymers 0.000 description 1
- 229920002223 polystyrene Polymers 0.000 description 1
- 150000003254 radicals Chemical class 0.000 description 1
- 150000003378 silver Chemical class 0.000 description 1
- CQLFBEKRDQMJLZ-UHFFFAOYSA-M silver acetate Chemical compound [Ag+].CC([O-])=O CQLFBEKRDQMJLZ-UHFFFAOYSA-M 0.000 description 1
- 229940071536 silver acetate Drugs 0.000 description 1
- 229940071575 silver citrate Drugs 0.000 description 1
- 229940100890 silver compound Drugs 0.000 description 1
- 150000003379 silver compounds Chemical class 0.000 description 1
- 229960001516 silver nitrate Drugs 0.000 description 1
- 235000010265 sodium sulphite Nutrition 0.000 description 1
- AKHNMLFCWUSKQB-UHFFFAOYSA-L sodium thiosulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=S AKHNMLFCWUSKQB-UHFFFAOYSA-L 0.000 description 1
- 235000019345 sodium thiosulphate Nutrition 0.000 description 1
- 229920003002 synthetic resin Polymers 0.000 description 1
- 239000000057 synthetic resin Substances 0.000 description 1
- UMGDCJDMYOKAJW-UHFFFAOYSA-N thiourea group Chemical group NC(=S)N UMGDCJDMYOKAJW-UHFFFAOYSA-N 0.000 description 1
- QUTYHQJYVDNJJA-UHFFFAOYSA-K trisilver;2-hydroxypropane-1,2,3-tricarboxylate Chemical compound [Ag+].[Ag+].[Ag+].[O-]C(=O)CC(O)(CC([O-])=O)C([O-])=O QUTYHQJYVDNJJA-UHFFFAOYSA-K 0.000 description 1
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 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
- G03C8/00—Diffusion transfer processes or agents therefor; Photosensitive materials for such processes
- G03C8/24—Photosensitive materials characterised by the image-receiving section
- G03C8/26—Image-receiving layers
- G03C8/28—Image-receiving layers containing development nuclei or compounds forming such nuclei
Definitions
- This invention relates to the reproduction of photographic images wherein a silver halide image is transferred imagewise to a receiving sheet for development and particularly to the constitution of such a receiving sheet.
- the exposed negative material is then treated with a developer composition containing a silver halide solvent and a silver halide developing agent after which the wet, exposed negative material is contacted with a receiving material comprising a piece of paper or foil containing a fogging agent and silver halide solvents.
- the devolper composition causes the development of the negative latent image in the negative paper; the silver halide solvents in said developer composition react with the unexposed silver halide to form soluble silver complexes which are transferred by diffusion to the receiving material and are there acted upon by the fogging agent therein, whereupon said silver halide complexes are transformed to metallic silver or silver compounds of high optical density.
- the receiving materials made in accordance with the above US. patent are prepared by coating gelatin from a water solution onto a base. This use of water, as the solvent, leads to problems such as long drying periods at fairly high temperatures and the tackiness so prevalent in such receiving materials is most likely due to its gelatin layer.
- a plastic foil base such as that from cellulose acetate, polystyrene, or the like, is coated with a solution comprising organic solvents together with a copolymer of maleic anhydride and an alkyl vinyl ether, a normally hydrophobic polymer such as cellulose acetate, vinyl acetate, or the like, a silver halide developing agent such as hydroquinone or paminophenol, a silver halide fogging agent such as Z-hydroxyethylallylthiourea, a water soluble silver salt such as silver nitrate, silver acetate, silver citrate, or the like, which, quite likely, aid in the nucleation needed to form dense images.
- a solution comprising organic solvents together with a copolymer of maleic anhydride and an alkyl vinyl ether, a normally hydrophobic polymer such as cellulose acetate, vinyl acetate, or the like
- a silver halide developing agent such as hydroquinone or paminophenol
- traces of an acid corresponding to the anion of the H 0 soluble silver salt are included in our coating solution such as nitric, acetic, citric acids, or the like.
- the function of the acid is to prevent the silver ion from being reduced by the developing agent before the coated foil has been dried.
- the polymer mixture used in coating the foil base is normally hydrophobic and, as such, Will not be evenly Wet with the aqueous developing solution used in processing.
- hydrophobic coatings when treated with certain hydrolytic agents, i.e., a moist nitrogen containing base, are transformed into hydrophilic films and, in this connection, reference is made to US. Patent 2,756,163 to Herrick and Amon.
- the foil coating readily accepts the developer compositions used after exposure.
- the surface hydrolysis of the alkyl vinyl ethermaleic anhydride copolymer coating With a water soluble nitrogenous base also neutralizes any mineral acid present.
- the foil base coated as above may also be coated on the back side with a solvent solution containing the alkyl vinyl ether-maleic anhydride copolymer and the hydrophobic polymer.
- alkyl vinyl ether-maleic anhydride copolymers contemplated for use are those described, for example, in US. Patent 2,772,972 and in US. application Serial No. 669,942, filed July 5, 1957, entitled Positive Working and Photomechanical Printing Plates.
- Such copolymers include those from maleic anhydride, on the one hand,
- the hydrophobic resin may be cellulose propionate, cellulose butyrate, mixed esters such as cellulose acetate propionate, cellulose acetate butyrate, polyvinyl acetals such as polyvinyl butyral, polymethyl acrylate, polymethylrnethacrylate, and the like.
- Alternates of the silver halide fogging agent may be employed and are described in US. Patent 2,755,185 and include N-allyl-4-morpholinethiocarbamate, 1-allyl-3- ethyl-Z-thiourea, 1-benzyl-3- 8-hydroxyethyl-2-thiourea, and the like.
- our new transfer foil produces, in a surprisingly short time, high contrast positive copies of originals with completely haze-free backgrounds free from-yellow discoloration.
- the moist foil is completely tack free and dries in a few seconds to a copy very suitable for use in producing further reproductions by, for instance, the diazotype copying process or for use as a master for producing printing plates in a photomechamcal repro-
- the use of the moist organic solvent system from which our transfer material is coated material ly speeds up coating operation with a subsequent saving in cost.
- our new receiving material possesses all of the properties and uses of the receiving material of the prior art.
- the photographic images formed on our receiving material may be given any of the subsequent treatments employed in photography such as intensification, reduction, toning, color development, build up of color images by silver bleaching, and the like.
- Example I Solution A is made by dissolving 50 g. of polyvinyl methyl ether-maleic anhydride (PVM/MA) with a specific viscosity in 2-butanone at 20 C. of 1.0-1.5, and 25 g. of low viscosity cellulose acetate containing 56% combined acetic acid in a mixture of acetone (3000 ml.) and methyl cellosolve acetate (250 ml).
- PVM/MA polyvinyl methyl ether-maleic anhydride
- Solution B contains methanol (1750 ml.), nitric acid (1.75 ml.), hydroquinone (5.0 g.) and 2-hydroxyethylallylthiourea (2.5 g.). To this is added silver nitrate (2.5 g.) dissolved in 5.0 ml. of water.
- Solution B is added to solution A and the resulting mixture is applied by reverse roll bead coating to give a concentration of about 5 ml. per sq. ft. to a cellulose triacetate film base. 7
- the foil After drying, the foil is overcoated with a solution of monoet-hanolamine (10% in water) using the reverse roll bead methodat a rate of 5.5 feet per minute and kept wet for about 1 minute before entering a drying chamber.
- the back side of the foil is now coated by reverse roll head with a solution formulated as solution A but containing methanol (1750 ml.) in addition. This too is overcoated with 10% monoethanolamine as described above.
- a piece of silver halide negative paper is exposed reflex-wise in a light box using an opaque original.
- the negative paper and receiving foil described above are passed through a developing device.
- the exposed negative and receiving foil are pressed face to' face in the presence of a developer solution containing a silv'er halide developing agent and a fixer such as hypo.
- a few seconds after emerging from the developing device image transfer from the negative to the receiving material is complete and the two sheets are peeled apart.
- the receiving foil only slightly damp, contains a completely clear black and white positive of the opaque original. 7
- a developing composition suitable for use in the above developing device is as follows:
- Example 11 4 A receiving .foil was prepared according to Example '1' except that the low viscosity cellulose acetate used therein for solution A was replaced by a vinyl acetate resin.
- Example Ill particular vinyl' acetate employedhad an intrinsic vis--' 4
- Example IV Using polyethyl vinyl ether-maleic anhydride in lieu of PVM/ MA, the procedure in this example was carried out as given in Example I.
- Example V Example VI Using 25.0 g. of a low viscosity, low hydroxyl polyvinyl butyral having a viscosity of 23 cps. (5% in ethanol) in lieu of the cellulose acetate, a cellulose acetate receiving foil was prepared, exposed and developed as in Example I. A clear black and white positive image of the opaque copy material was obtained.
- Example VII The procedure of Example I was carried out using polybutyl vinyl ether-maleic anhydride in lieu of PVM/ MA. The results were parallel to those obtained in Example 1.
- Example VIII The procedure of Example I was carried out using polyvinyl isobutyl ether-maleic anhydride in lieu of 'PVM/MA. The results were parallel to those obtained in Example I.
- Example IX The procedure of Example I was carried out using poly-2-methoxyethyl vinyl ether-maleic anhydride in lieu of 'PVM/ MA. The results were parallel to those obtained v in Example I.
- a receiving material for use in the photographic difiusion-transfer process comprising a support having thereon a water receptive layer comprising an alkali treated mixture of a polyalkyl vinyl ether-maleic anhydride co-polymer and a hydrophobic resin compatible therewith, a silver halide developing agent, a fogging agent capable of transforming a soluble silver halide image into an image of high optical opacity and a water soluble silver salt.
- polyalkyl vinyl ether-maleic anhydride co-polymer is polyvinyl methyl ether-maleic anhydride co-polymer.
- the fogging agent is a thiourea derivative, one nitrogen atom of which is joined through a methylene group to a grouping of carbon atoms containing a :C radical directly linked to said methylene group, and the other nitrogen atom of which is'strongly basic by virtue of a chemical structure selected from the class consisting of those in which the nitrogen atom is substituted by an aliphatic radical and those in which the nitrogen atom forms part of a saturated heterocyclic ring.
Landscapes
- Physics & Mathematics (AREA)
- General Physics & Mathematics (AREA)
- Silver Salt Photography Or Processing Solution Therefor (AREA)
- Non-Silver Salt Photosensitive Materials And Non-Silver Salt Photography (AREA)
Priority Applications (4)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
BE578365D BE578365A (en(2012)) | 1958-05-07 | ||
DENDAT1073306D DE1073306B (de) | 1958-05-07 | Bildempfangsmaterial zur Verwendung im photographischen Silbersalzdiffusions-Ubertragungsverfahren und Verfahren zu dessen Herstellung | |
US733505A US3015562A (en) | 1958-05-07 | 1958-05-07 | Receiving sheet for use in photographic silver transfer process |
GB14146/59A GB856792A (en) | 1958-05-07 | 1959-04-24 | Receiving sheet for use in photographic silver transfer process |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US733505A US3015562A (en) | 1958-05-07 | 1958-05-07 | Receiving sheet for use in photographic silver transfer process |
Publications (1)
Publication Number | Publication Date |
---|---|
US3015562A true US3015562A (en) | 1962-01-02 |
Family
ID=24947891
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US733505A Expired - Lifetime US3015562A (en) | 1958-05-07 | 1958-05-07 | Receiving sheet for use in photographic silver transfer process |
Country Status (4)
Country | Link |
---|---|
US (1) | US3015562A (en(2012)) |
BE (1) | BE578365A (en(2012)) |
DE (1) | DE1073306B (en(2012)) |
GB (1) | GB856792A (en(2012)) |
Cited By (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3257205A (en) * | 1960-10-12 | 1966-06-21 | Gevaert Photo Prod Nv | Method for heat development |
US3630734A (en) * | 1969-03-12 | 1971-12-28 | Eastman Kodak Co | Photographic diffusion transfer product and process |
FR2130719A1 (en(2012)) * | 1971-03-26 | 1972-11-03 | Fuji Photo Film Co Ltd | |
FR2184794A1 (en(2012)) * | 1972-05-15 | 1973-12-28 | Fuji Photo Film Co Ltd | |
US4038077A (en) * | 1974-04-04 | 1977-07-26 | Polaroid Corporation | Process comprising diffusion transfer silver image removal |
Families Citing this family (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
NL259197A (en(2012)) * | 1960-12-17 | |||
BE635438A (en(2012)) * | 1962-07-28 | |||
US4029849A (en) | 1974-11-05 | 1977-06-14 | Eastman Kodak Company | Cover sheets with timing layer comprising cellulose acetate and copolymer of maleic anhydride |
JP2000509374A (ja) | 1996-04-19 | 2000-07-25 | アルファ セラピュティック コーポレイション | 凍結乾燥した血液タンパク質のウイルス不活性化方法 |
Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2704721A (en) * | 1954-04-22 | 1955-03-22 | Polaroid Corp | Photographic diffusion transfer reversal processes |
US2751300A (en) * | 1954-07-15 | 1956-06-19 | Eastman Kodak Co | Photographic solvent transfer reproduction process |
US2756163A (en) * | 1952-01-04 | 1956-07-24 | Gen Aniline & Film Corp | Resinous layers having a selected degree of water sensitivity and method of making same |
US2882151A (en) * | 1955-10-31 | 1959-04-14 | Eastman Kodak Co | Photographic roll film transfer process |
-
0
- BE BE578365D patent/BE578365A/xx unknown
- DE DENDAT1073306D patent/DE1073306B/de active Pending
-
1958
- 1958-05-07 US US733505A patent/US3015562A/en not_active Expired - Lifetime
-
1959
- 1959-04-24 GB GB14146/59A patent/GB856792A/en not_active Expired
Patent Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2756163A (en) * | 1952-01-04 | 1956-07-24 | Gen Aniline & Film Corp | Resinous layers having a selected degree of water sensitivity and method of making same |
US2704721A (en) * | 1954-04-22 | 1955-03-22 | Polaroid Corp | Photographic diffusion transfer reversal processes |
US2751300A (en) * | 1954-07-15 | 1956-06-19 | Eastman Kodak Co | Photographic solvent transfer reproduction process |
US2882151A (en) * | 1955-10-31 | 1959-04-14 | Eastman Kodak Co | Photographic roll film transfer process |
Cited By (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3257205A (en) * | 1960-10-12 | 1966-06-21 | Gevaert Photo Prod Nv | Method for heat development |
US3630734A (en) * | 1969-03-12 | 1971-12-28 | Eastman Kodak Co | Photographic diffusion transfer product and process |
FR2130719A1 (en(2012)) * | 1971-03-26 | 1972-11-03 | Fuji Photo Film Co Ltd | |
FR2184794A1 (en(2012)) * | 1972-05-15 | 1973-12-28 | Fuji Photo Film Co Ltd | |
US4038077A (en) * | 1974-04-04 | 1977-07-26 | Polaroid Corporation | Process comprising diffusion transfer silver image removal |
Also Published As
Publication number | Publication date |
---|---|
DE1073306B (de) | 1960-01-14 |
GB856792A (en) | 1960-12-21 |
BE578365A (en(2012)) |
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