US3368891A - Process for the manufacture of photographic material containing oxidized polysaccharides - Google Patents
Process for the manufacture of photographic material containing oxidized polysaccharides Download PDFInfo
- Publication number
- US3368891A US3368891A US350686A US35068664A US3368891A US 3368891 A US3368891 A US 3368891A US 350686 A US350686 A US 350686A US 35068664 A US35068664 A US 35068664A US 3368891 A US3368891 A US 3368891A
- Authority
- US
- United States
- Prior art keywords
- layer
- pigment
- photographic material
- pigment layer
- manufacture
- 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
- 229920001282 polysaccharide Polymers 0.000 title description 27
- 239000005017 polysaccharide Substances 0.000 title description 27
- 238000000034 method Methods 0.000 title description 15
- 230000008569 process Effects 0.000 title description 12
- 239000000463 material Substances 0.000 title description 10
- 238000004519 manufacturing process Methods 0.000 title description 6
- 150000004676 glycans Chemical class 0.000 title 1
- 239000000049 pigment Substances 0.000 description 41
- 150000004804 polysaccharides Chemical class 0.000 description 26
- 239000005018 casein Substances 0.000 description 12
- BECPQYXYKAMYBN-UHFFFAOYSA-N casein, tech. Chemical compound NCCCCC(C(O)=O)N=C(O)C(CC(O)=O)N=C(O)C(CCC(O)=N)N=C(O)C(CC(C)C)N=C(O)C(CCC(O)=O)N=C(O)C(CC(O)=O)N=C(O)C(CCC(O)=O)N=C(O)C(C(C)O)N=C(O)C(CCC(O)=N)N=C(O)C(CCC(O)=N)N=C(O)C(CCC(O)=N)N=C(O)C(CCC(O)=O)N=C(O)C(CCC(O)=O)N=C(O)C(COP(O)(O)=O)N=C(O)C(CCC(O)=N)N=C(O)C(N)CC1=CC=CC=C1 BECPQYXYKAMYBN-UHFFFAOYSA-N 0.000 description 12
- 235000021240 caseins Nutrition 0.000 description 12
- 108010073771 Soybean Proteins Proteins 0.000 description 11
- 235000019710 soybean protein Nutrition 0.000 description 11
- 239000003513 alkali Substances 0.000 description 10
- 150000001447 alkali salts Chemical class 0.000 description 10
- 150000003863 ammonium salts Chemical class 0.000 description 10
- 239000011230 binding agent Substances 0.000 description 9
- TZCXTZWJZNENPQ-UHFFFAOYSA-L barium sulfate Chemical compound [Ba+2].[O-]S([O-])(=O)=O TZCXTZWJZNENPQ-UHFFFAOYSA-L 0.000 description 8
- 125000003172 aldehyde group Chemical group 0.000 description 7
- 125000003198 secondary alcohol group Chemical group 0.000 description 7
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 6
- 239000004332 silver Substances 0.000 description 6
- 229910052709 silver Inorganic materials 0.000 description 6
- 229920000945 Amylopectin Polymers 0.000 description 5
- 239000007864 aqueous solution Substances 0.000 description 5
- ZNZYKNKBJPZETN-WELNAUFTSA-N Dialdehyde 11678 Chemical class N1C2=CC=CC=C2C2=C1[C@H](C[C@H](/C(=C/O)C(=O)OC)[C@@H](C=C)C=O)NCC2 ZNZYKNKBJPZETN-WELNAUFTSA-N 0.000 description 4
- 229920002085 Dialdehyde starch Polymers 0.000 description 4
- 108010010803 Gelatin Proteins 0.000 description 4
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 4
- 238000009792 diffusion process Methods 0.000 description 4
- 229920000159 gelatin Polymers 0.000 description 4
- 239000008273 gelatin Substances 0.000 description 4
- 235000019322 gelatine Nutrition 0.000 description 4
- 235000011852 gelatine desserts Nutrition 0.000 description 4
- 239000000203 mixture Substances 0.000 description 4
- 239000000243 solution Substances 0.000 description 4
- 239000000725 suspension Substances 0.000 description 4
- VHUUQVKOLVNVRT-UHFFFAOYSA-N Ammonium hydroxide Chemical compound [NH4+].[OH-] VHUUQVKOLVNVRT-UHFFFAOYSA-N 0.000 description 3
- BQCADISMDOOEFD-UHFFFAOYSA-N Silver Chemical compound [Ag] BQCADISMDOOEFD-UHFFFAOYSA-N 0.000 description 3
- 229920002472 Starch Polymers 0.000 description 3
- 230000009471 action Effects 0.000 description 3
- QGZKDVFQNNGYKY-UHFFFAOYSA-N ammonia Natural products N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 3
- 239000007900 aqueous suspension Substances 0.000 description 3
- 238000001035 drying Methods 0.000 description 3
- 239000004848 polyfunctional curative Substances 0.000 description 3
- 150000003839 salts Chemical class 0.000 description 3
- -1 silver halides Chemical class 0.000 description 3
- 239000008107 starch Substances 0.000 description 3
- 235000019698 starch Nutrition 0.000 description 3
- 239000000126 substance Substances 0.000 description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 3
- 239000000839 emulsion Substances 0.000 description 2
- 230000002209 hydrophobic effect Effects 0.000 description 2
- 230000003647 oxidation Effects 0.000 description 2
- 238000007254 oxidation reaction Methods 0.000 description 2
- JQWHASGSAFIOCM-UHFFFAOYSA-M sodium periodate Chemical compound [Na+].[O-]I(=O)(=O)=O JQWHASGSAFIOCM-UHFFFAOYSA-M 0.000 description 2
- 230000007480 spreading Effects 0.000 description 2
- OGIDPMRJRNCKJF-UHFFFAOYSA-N titanium oxide Inorganic materials [Ti]=O OGIDPMRJRNCKJF-UHFFFAOYSA-N 0.000 description 2
- 244000215068 Acacia senegal Species 0.000 description 1
- 229920002134 Carboxymethyl cellulose Polymers 0.000 description 1
- 244000287680 Garcinia dulcis Species 0.000 description 1
- 229920000084 Gum arabic Polymers 0.000 description 1
- 241001527806 Iti Species 0.000 description 1
- 229920002230 Pectic acid Polymers 0.000 description 1
- 239000000205 acacia gum Substances 0.000 description 1
- 235000010489 acacia gum Nutrition 0.000 description 1
- 230000002411 adverse Effects 0.000 description 1
- 239000000783 alginic acid Substances 0.000 description 1
- 235000010443 alginic acid Nutrition 0.000 description 1
- 229920000615 alginic acid Polymers 0.000 description 1
- 229960001126 alginic acid Drugs 0.000 description 1
- 150000004781 alginic acids Chemical class 0.000 description 1
- 238000003490 calendering Methods 0.000 description 1
- 239000001768 carboxy methyl cellulose Substances 0.000 description 1
- 235000010948 carboxy methyl cellulose Nutrition 0.000 description 1
- 239000008112 carboxymethyl-cellulose Substances 0.000 description 1
- 230000015271 coagulation Effects 0.000 description 1
- 238000005345 coagulation Methods 0.000 description 1
- 239000011248 coating agent Substances 0.000 description 1
- 238000000576 coating method Methods 0.000 description 1
- 239000000084 colloidal system Substances 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 230000001419 dependent effect Effects 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- 230000006872 improvement Effects 0.000 description 1
- 230000001788 irregular Effects 0.000 description 1
- 229920002521 macromolecule Polymers 0.000 description 1
- WSFSSNUMVMOOMR-NJFSPNSNSA-N methanone Chemical compound O=[14CH2] WSFSSNUMVMOOMR-NJFSPNSNSA-N 0.000 description 1
- 229920000609 methyl cellulose Polymers 0.000 description 1
- 239000001923 methylcellulose Substances 0.000 description 1
- 235000010981 methylcellulose Nutrition 0.000 description 1
- LCLHHZYHLXDRQG-ZNKJPWOQSA-N pectic acid Chemical compound O[C@@H]1[C@@H](O)[C@@H](O)O[C@H](C(O)=O)[C@@H]1OC1[C@H](O)[C@@H](O)[C@@H](OC2[C@@H]([C@@H](O)[C@@H](O)[C@H](O2)C(O)=O)O)[C@@H](C(O)=O)O1 LCLHHZYHLXDRQG-ZNKJPWOQSA-N 0.000 description 1
- 230000000149 penetrating effect Effects 0.000 description 1
- KHIWWQKSHDUIBK-UHFFFAOYSA-N periodic acid Chemical compound OI(=O)(=O)=O KHIWWQKSHDUIBK-UHFFFAOYSA-N 0.000 description 1
- 239000010318 polygalacturonic acid Substances 0.000 description 1
- 150000003214 pyranose derivatives Chemical group 0.000 description 1
- 239000004408 titanium dioxide Substances 0.000 description 1
- 229920001221 xylan Polymers 0.000 description 1
- 150000004823 xylans Chemical class 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
- G03C8/42—Structural details
- G03C8/52—Bases or auxiliary layers; Substances therefor
-
- 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
- G03C1/00—Photosensitive materials
- G03C1/76—Photosensitive materials characterised by the base or auxiliary layers
- G03C1/775—Photosensitive materials characterised by the base or auxiliary layers the base being of paper
- G03C1/79—Macromolecular coatings or impregnations therefor, e.g. varnishes
-
- 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
- G03G5/14—Inert intermediate or cover layers for charge-receiving layers
- G03G5/142—Inert intermediate layers
Definitions
- the pigment layer contains as a binding agent an alkali or ammonium salt of casein or soybean protein and is hardened by means of a polysaccharide which has at least some, preferably 50-100%, of its secondary alcohol groups converted into aldehyde groups, or water-soluble derivatives of such polysaccharides.
- Photographic paper is generally composed of the following layers.
- a so-called pigment layer usually coated from a dispersion of a pigment such as barium sulfate, titanium dioxide, etc., in a hydrophilic or hydrophobic colloid as binding agent,
- the actual image-layer which may be a light-sensitive layer or a layer containing development nuclei wherein an image can be formed according to the silver complex diffusion transfer process.
- all pigments applied in the paper industry for sized paper may be used for the pigment layer with the proviso, however, that said pigments do not adversely affect the light-sensitive layer or the development nuclei.
- the photographic paper may still comprise other layers, e.g., a subbing layer improving the adhesion of the light-sensitive layer to the pigment layer containing a hydrophobic binding agent, a filter layer, etc.
- light-sensitive layer used in the description and the claims is meant not only light-sensitive layers on the basis of silver halides or other light-sensitive compounds but also layers containing photoconductive pigments for use in electrophotography.
- the properties of the photographic material are dependent on the quality of the light-sensitive layer or of the layer containing development nuclei, of the pigment layer and of the paper support.
- the physical irregularities of the surface of the pigment layer are reproduced in the light-sensitive layer and after processing said irregular ities, often enlarged, can be observed in the light-sensitive layer since they prevent to obtain a light-sensitive layer of uniform thickness. Therefore the surface of the pigment layer should be as uniform as possible in view of obtaining a product of maximum quality.
- hydrophilic binding agent for the pigment layer is generally used gelatin in the presence of formaldehyde.
- formaldehyde for preventing the aqueous gelatin solution from penetrating too strongly into the paper support the gelatin is gelled by cooling which also facilitates the further treatment of the sized paper support.
- gelatin hardened by means of formaldehyde however, entails some disadvantages on the pigment layer among others:
- the process according to the invention for the manufacture of photographic material comprising a paper support and a pigment layer applied thereto, is characterized in that said pigment layer is formed from a suspension of a pigment in an aqueous solution of an alkali or ammonium salt of casein or of soybean protein to which anaqueous solution of an oxidized polysaccharide or of a water-soluble derivative of an oxidized polysaccharide has been added.
- .oxidized polysacharides stands for oxidized polysaccharides as well as for their water-soluble derivatives.
- the oxidized polysaccharides are obtained by treating polysaccharides With an aqueous solution of a periodate such an sodium periodate. By this treatment the secondary alcohol groups of the pyranose units of the polysaccharide are at least partially converted into aldehyde groups. Best results are obtained when from 50 to of the secondary alcohol groups are converted into aldehyde groups.
- Polysaccharides which are especially suited for being oxidized and used according to the present invention are; starch, watersolu ble polysaccharides such as carboxymethyl cellulose, water-soluble methyl cellulose, watersoluble derivatives of starch, polysaccharides the dialdehyde derivatives of which are water-soluble such as amylopectine, further alginic acid and salts thereof, pectic acid and salt thereof, gum arabic and xylan.
- the hardening action of the oxidized polysaccharide upon the alkali or ammonium salt of casein or of soybean protein increases with the concentration of oxidized polysaccharide and with the number of aldehyde groups present in its macromolecule.
- the amount 'of oxidized polysaccharide added depends on the hardening degree. desired; it lies, however, generally between 0.5 and 50% by weight and preferably between 1 and 7% by weight relative to the amount of dry alkali or ammonium salt of casein or of soybean protein.
- the amount of alkali or ammonium salt itself lies between 5 and 50%, preferably between 6 and 10% by weight relative to the amount of dry pigment.
- photographically inert pigment barium sulphate is preferably used although titanium oxide and other inert pigments are also suited.
- the suspension of pigment in alkali or ammonium salt 0 of casein or of soybean protein, together with oxidized polysaccharide is coated onto the paper web in such a way that after uniformly spreading out and drying from 10 to 3 60 g. per sq. m. of dry substance is present. Occasionally the amount of dry substance may fall outside these limits.
- the pigment suspension may be applied as a layer to the paper support by means of an air knife, brushes or any other spreading machine.
- the pigment layer according to the invention may successfully be coated upon paper supports destined for the manufacture of photographic paper.
- Onto said pigment layer one or more light-sensitive photographic layers may be coated, for instance one or more light-sensitive gelatino silver halide emulsion layers.
- the pigment layer described above may also be successfully applied in photographic papers destined for electrophotographic applications. In that case the pigment layer or a layer applied thereto should contain photoconductive substances of use in electrophotography.
- the pigment layer may further be applied in non-light-sensitive photographic paper, for instance in the positive image-receiving material destined for producing images according to the silver complex diffusion transfer process.
- Example I To a paper web a pigment layer is applied from the following composition according to known methods:
- the dialdehyde amylopectin was obtained by oxidation into aldehyde groups of 55% of the secondary alcohol groups of the amylopectin.
- Example 3 To a paper web a pigment layer is applied from the following composition according to known methods;
- the dialdehyde starch was obtained by oxidation of 78% of the secondary alcohol groups of starch.
- the smoothness of the surface and the hardening are favourably influenced by calendering at elevated temperatures for instance at 60 C.
- a process for manufacturing photographic material comprising a paper support and a pigment layer carried on said support, the improvement which comprises forming said pigment layer from a suspension of a pigment in an aqueous solution of an alkali or ammonium salt of casein or soybean protein, said aqueous solution having incorporated therein a polysaccharide having the secondary alcohol groups thereof at least partially converted into aldehyde groups or a water-soluble derivative of said aldehyde-modified polysaccharide.
- aldehyde-modified polysaccharide is dialdehyde amylopectin.
- Photographic material according to claim 1 wherein at least one light-sensitive silver halide emulsion layer is applied to the pigment layer.
- Photographic material obtained according to claim 1 for use in electrophotography wherein a layer selected from said pigment layer and a layer applied thereto contains photoconductive pigments.
Landscapes
- Physics & Mathematics (AREA)
- General Physics & Mathematics (AREA)
- Engineering & Computer Science (AREA)
- Architecture (AREA)
- Structural Engineering (AREA)
- Spectroscopy & Molecular Physics (AREA)
- Chemical & Material Sciences (AREA)
- Materials Engineering (AREA)
- Paper (AREA)
- Photoreceptors In Electrophotography (AREA)
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
BE629458 | 1963-03-12 |
Publications (1)
Publication Number | Publication Date |
---|---|
US3368891A true US3368891A (en) | 1968-02-13 |
Family
ID=3845449
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US350686A Expired - Lifetime US3368891A (en) | 1963-03-12 | 1964-03-10 | Process for the manufacture of photographic material containing oxidized polysaccharides |
Country Status (4)
Country | Link |
---|---|
US (1) | US3368891A (enrdf_load_stackoverflow) |
BE (1) | BE629458A (enrdf_load_stackoverflow) |
DE (1) | DE1447688A1 (enrdf_load_stackoverflow) |
GB (1) | GB1040376A (enrdf_load_stackoverflow) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4542093A (en) * | 1983-07-26 | 1985-09-17 | Fuji Photo Film Co., Ltd. | Photographic silverhalide material containing two subbing layers |
US5254450A (en) * | 1992-12-09 | 1993-10-19 | Eastman Kodak Company | Hydrophobically substituted amylose starch-sized photographic paper support and photographic element containing same |
Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB891221A (en) * | 1957-04-08 | 1962-03-14 | Gevaert Photo Production N V | Improvements in or relating to the production of hardened gelatin layers in materials for photographic purposes |
-
0
- BE BE629458D patent/BE629458A/xx unknown
-
1964
- 1964-03-10 US US350686A patent/US3368891A/en not_active Expired - Lifetime
- 1964-03-12 DE DE19641447688 patent/DE1447688A1/de active Pending
- 1964-03-12 GB GB10557/64A patent/GB1040376A/en not_active Expired
Patent Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB891221A (en) * | 1957-04-08 | 1962-03-14 | Gevaert Photo Production N V | Improvements in or relating to the production of hardened gelatin layers in materials for photographic purposes |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4542093A (en) * | 1983-07-26 | 1985-09-17 | Fuji Photo Film Co., Ltd. | Photographic silverhalide material containing two subbing layers |
US5254450A (en) * | 1992-12-09 | 1993-10-19 | Eastman Kodak Company | Hydrophobically substituted amylose starch-sized photographic paper support and photographic element containing same |
Also Published As
Publication number | Publication date |
---|---|
BE629458A (enrdf_load_stackoverflow) | |
DE1447688A1 (de) | 1969-01-23 |
GB1040376A (en) | 1966-08-24 |
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