US2315966A - Photographic emulsion - Google Patents
Photographic emulsion Download PDFInfo
- Publication number
- US2315966A US2315966A US387446A US38744641A US2315966A US 2315966 A US2315966 A US 2315966A US 387446 A US387446 A US 387446A US 38744641 A US38744641 A US 38744641A US 2315966 A US2315966 A US 2315966A
- Authority
- US
- United States
- Prior art keywords
- emulsion
- resin
- photographic
- developing agent
- grams
- 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
- 239000000839 emulsion Substances 0.000 title description 52
- 239000011347 resin Substances 0.000 description 36
- 229920005989 resin Polymers 0.000 description 36
- QIGBRXMKCJKVMJ-UHFFFAOYSA-N Hydroquinone Chemical compound OC1=CC=C(O)C=C1 QIGBRXMKCJKVMJ-UHFFFAOYSA-N 0.000 description 21
- 239000003795 chemical substances by application Substances 0.000 description 21
- 239000000243 solution Substances 0.000 description 13
- 239000000463 material Substances 0.000 description 11
- CPELXLSAUQHCOX-UHFFFAOYSA-M Bromide Chemical compound [Br-] CPELXLSAUQHCOX-UHFFFAOYSA-M 0.000 description 5
- 229920001800 Shellac Polymers 0.000 description 5
- ZLGIYFNHBLSMPS-ATJNOEHPSA-N shellac Chemical compound OCCCCCC(O)C(O)CCCCCCCC(O)=O.C1C23[C@H](C(O)=O)CCC2[C@](C)(CO)[C@@H]1C(C(O)=O)=C[C@@H]3O ZLGIYFNHBLSMPS-ATJNOEHPSA-N 0.000 description 5
- 229940113147 shellac Drugs 0.000 description 5
- 235000013874 shellac Nutrition 0.000 description 5
- 239000004208 shellac Substances 0.000 description 5
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 4
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 4
- 238000000576 coating method Methods 0.000 description 4
- 239000006185 dispersion Substances 0.000 description 4
- 238000004519 manufacturing process Methods 0.000 description 4
- 239000003960 organic solvent Substances 0.000 description 4
- GEHJYWRUCIMESM-UHFFFAOYSA-L sodium sulfite Chemical compound [Na+].[Na+].[O-]S([O-])=O GEHJYWRUCIMESM-UHFFFAOYSA-L 0.000 description 4
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 3
- 239000002585 base Substances 0.000 description 3
- 238000000034 method Methods 0.000 description 3
- IOLCXVTUBQKXJR-UHFFFAOYSA-M potassium bromide Inorganic materials [K+].[Br-] IOLCXVTUBQKXJR-UHFFFAOYSA-M 0.000 description 3
- 150000003839 salts Chemical class 0.000 description 3
- 229910052709 silver Inorganic materials 0.000 description 3
- 239000004332 silver Substances 0.000 description 3
- 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 description 3
- CBCKQZAAMUWICA-UHFFFAOYSA-N 1,4-phenylenediamine Chemical compound NC1=CC=C(N)C=C1 CBCKQZAAMUWICA-UHFFFAOYSA-N 0.000 description 2
- 239000001828 Gelatine Substances 0.000 description 2
- 238000010521 absorption reaction Methods 0.000 description 2
- 239000012670 alkaline solution Substances 0.000 description 2
- 239000011248 coating agent Substances 0.000 description 2
- 235000019441 ethanol Nutrition 0.000 description 2
- 229920000159 gelatin Polymers 0.000 description 2
- 235000019322 gelatine Nutrition 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Chemical compound [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 description 2
- SQGYOTSLMSWVJD-UHFFFAOYSA-N silver(1+) nitrate Chemical compound [Ag+].[O-]N(=O)=O SQGYOTSLMSWVJD-UHFFFAOYSA-N 0.000 description 2
- 235000010265 sodium sulphite Nutrition 0.000 description 2
- 239000002904 solvent Substances 0.000 description 2
- 238000010186 staining Methods 0.000 description 2
- 125000001424 substituent group Chemical group 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- CDAWCLOXVUBKRW-UHFFFAOYSA-N 2-aminophenol Chemical class NC1=CC=CC=C1O CDAWCLOXVUBKRW-UHFFFAOYSA-N 0.000 description 1
- 241000592335 Agathis australis Species 0.000 description 1
- 240000000972 Agathis dammara Species 0.000 description 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 1
- 239000004859 Copal Substances 0.000 description 1
- 229920002871 Dammar gum Polymers 0.000 description 1
- 241000782205 Guibourtia conjugata Species 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
- 101100490488 Mus musculus Add3 gene Proteins 0.000 description 1
- 229920000175 Pistacia lentiscus Polymers 0.000 description 1
- BQCADISMDOOEFD-UHFFFAOYSA-N Silver Chemical compound [Ag] BQCADISMDOOEFD-UHFFFAOYSA-N 0.000 description 1
- 239000003513 alkali Substances 0.000 description 1
- 229920002678 cellulose Polymers 0.000 description 1
- 239000001913 cellulose Substances 0.000 description 1
- 229920002301 cellulose acetate Polymers 0.000 description 1
- 239000000084 colloidal system Substances 0.000 description 1
- 230000007547 defect Effects 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 125000000687 hydroquinonyl group Chemical group C1(O)=C(C=C(O)C=C1)* 0.000 description 1
- 238000007654 immersion Methods 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- 150000004986 phenylenediamines Chemical class 0.000 description 1
- 229910000027 potassium carbonate Inorganic materials 0.000 description 1
- 239000002244 precipitate Substances 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- 229910001961 silver nitrate Inorganic materials 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 230000003019 stabilising effect Effects 0.000 description 1
- LSNNMFCWUKXFEE-UHFFFAOYSA-L sulfite Chemical compound [O-]S([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-L 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
- G03C1/00—Photosensitive materials
- G03C1/005—Silver halide emulsions; Preparation thereof; Physical treatment thereof; Incorporation of additives therein
- G03C1/06—Silver halide emulsions; Preparation thereof; Physical treatment thereof; Incorporation of additives therein with non-macromolecular additives
- G03C1/42—Developers or their precursors
Description
Patented Apr. 6, 1943 PHOTOGRAPHIO EMULSION Edward Bowes Knott, Wealdstone, England, as-
signor to Eastman Kodak Company. Rochester,
N. Y., a corporation of New Jersey No Drawing. Application April 8, 1941, Serial No. 387,446. In Great Britain April 15, 1940 Claims.
This invention relates to the production of sensitive photographic films, plates, papers and similar materials, and is more especially concerned with the production of so-called selfdevelopable photographic materials, that is to say materials which already contain photographic developing agents and which after exposure can be developed simply by treatment with an alkaline solution.
It has long been known to incorporate photographic developing agents such as hydroquinone in sensitive photographic emulsions, so that photographic plates and similar materials coated with the emulsions can be developed by means of simple alkaline solutions, but one difilculty arising in the production of such materials has been that the emulsions are unduly liable to give fogged or stained images owing to the presence of the developing agent.
(me object of my inventionis a self-developing sensitive photographic material which gives images free from stain.
Another object of my invention is a rapid selfdeveloping photographic material.
Another object of my invention is a photographic material containing a developing agent having an improved degree of dispersion.
Another object of my invention is the production of stabilized emulsions by means of resinous shellac fractions.
Other objects will appear hereinafter.
According to my invention there is provided a self-developable photographic silver salt emulsion containing a photographic developing agent and having a pH of less than about 6.5. The pH should not be above about 6.9 and a preferred pH is 6.0.
The amount of developing agent dispersed in the emulsion should be sufficient to give a satisfactory image on developing a fully exposed portion of the emulsion. Such development may be done by immersion in a suitable alkaline bath. Usually the amount of developing agent, such as hydroquinone, should be more than about 3 and preferably more than 6 grams per litre of the usual type of emulsion.
when the emulsion has a pH above '7 before addition of the developing agent, the pH should first be adjusted to a value below 'I, then if addition of the developing agent, such as hydroquinone, produces a lowering of the pH to say 4, it may be re-adjusted to a higher value, say 6.0 before the emulsion is coated, whereas if the addition of the developing agent, such as a para phenylene diamine base, produces a rise in the pH, it is desirable to adjust the pH either before or during the addition of the developing agent so that it never rises above '7.
Whatever the pH value improved results are obtained (especially where plates and films are being made) if a substantially water-insoluble resin is dispersed through the emulsion in addl tion to the developing agent. This can readily be effected by dissolving the resin in a solvent (usually ethyl alcohol, acetone or other organic solvent) and adding the solution to the liquid photographic emulsion so that the resin is precipitated to form a dispersion in the emulsion. The developing agent can be introduced into the emulsion before, during or after addition of the resin, and a good method of procedure is to employ a developing agent soluble in an organic solvent which is also a solvent for the resin and to add a solution of the two in the organic solvent to the emulsion. If desired, the resin solution can be added to a gelatine or similar solution to form a dispersion which is then itself added to the photographic emulsion, and in this case the developing agent can also be incorporated in the gelatine or similar solution, for instance by adding it to the resin solution.
The developing agent is preferably hydroquinone or a derivative thereof, although others can be used, e. g. aminophenols and phenylene diamines and derivatives thereof. Furthermore, the developing agent may be one into the molecule of which has been introduced a substituent (which may be high molecular), although the substituent should preferably not be one which greatly reduces the solubility. It is naturally preferable not to employ developers which give undue staining on account of aerial oxidation for instance; p-phenylene diamine is somewhat liable to this defect, although it can be used if there is no objection to the stain which might be produced.
It will be appreciated that a substantially water-insoluble resin is required in order that a dispersion of the resin (as distinct from a solution) can be formed in the photographic emulsion, which is essentially an aqueous'liquid. Many resins, natural and synthetic, are suitable, for
instance whole shellac, hard shellac, soft shellac, hydrolysed soft shellac,-colophony and glyptal resins. Gum mastic, dammar, sandarach, copal, kauri and eoumarone resins are also suitable,
' although they are not perhaps as good as those given in the last sentence. Sodium and other salts of the resins can also be used, and it is to be understood that such salts are included in the term resins"; if, as is preferable, the final pH value of the emulsion is to be below '7, it may be necessary when using such salts (or when using other resins, for that matter) to ach'ust the pH value after their addition. To obtain a fine precipitate of the resin when it is added in the form of a solution in an organic solvent to the emulsion it is preferable that the concentration of the resin solution should be below about 10% in general, although this depends upon the resin used. The advantageous eifect of the resin appears to depend on the thickness of the emulsion, the greater this thickness the greater the stabilising effect of the resin. With very thin emulsions as used in certain printing papers, for instance, the effect is quite small, and in this case especially a very satisfactory product can be obtained simply by adjusting the pH value to below 7, as described above, without adding any resin at all.
It has been found that while in some cases esj pecially where a paper support is used the presence of the resin is liable to cause a slight loss of speed, this loss can be partly at least made up by incubating the emulsion for a period of say seven days. Furthermore, an antifoggant' can be incorporated in the emulsion, although this is not necessary.
The invention is applicable to self-developable emulsions in general, including those prepared from normal bromide emulsions, unwashed chloride emulsions, cinematograph positive emulsions and mixed emulsions for use in producing A self-developable emulsion for use in coating photographic plates is prepared by adding a solution of 25-125 grams of hydroquinone (preferably 50 grams) and 50-200 grams of soft lac resin (preferably 100 grams) in 1500 cc. of ethyl alcohol (spirit) for each 100 grams of resin to 8 litres of a contrast bromide emulsion of pH value approximately 6 and containing in the 8 litres a silver content equivalent to 200 grams of silver nitrate, and then adjusting the pH value to 6.0. The ratio of lac:hydroquinone used in this example is preferably higher than one.
EXAMPLE 2 Another example of a "self-developable emulsion is one prepared by adding a solution of 50 grams hydroquinone and 50 grams of Glyptal SB 102 resin in 750 cc. of acetone to 8 litres of a contrast bromide emulsion of the characteristics described in Example 1, and then adjusting the pH value to 6.0 as before. In general, less Glyptal SB 102 resin is required than if soft lac resin is used, and less resin is required when thin coatings of the emulsion are to be used.
Emu: 3
Another example of a "self-developable emulsion for paper coatings is one prepared by adding a solution of 200 grams hydroquinone in 500 cc. spirit to 8 litres of a bromide emulsion of the characteristics described in Example 1 and then adjusting the pH value to 6.0 as before. If the emulsion is applied to a paper base an increased hydroquinone content is preferable on account of absorption by the base, although this absorption can be reduced by applying a resinous or other substratum to the paper before applying the emulsion.
The alkaline baths used in developing the self-developable emulsions of the invention can be of various types, and a simple solution of an alkali can be used, although the presence of sulphite is desirable to reduce any tendency to staining and that of bromide to reduce any tendency to fogging, especially if the bath is to be used repeatedly. Two suitable developing baths are given by way of example below:
Developing bath. for rapid development (e. a.
5-15 seconds) Potassium hydroxide grams Sodium sulphite do- Potassium bromide do 10 Water to make cc. 1000 A photographic paper prepared according to the invention can be left in this bath for periods up to some minutes without substantial fogging.
Developing bath for normal development (c. g.
' 2 minutes) I Potassium carbonate grams 250 Sodium sulphite do 40 Potassium bromide do 10 Water to make -cc. 1000 In conclusion, while the invention has been described above with reference to the use of natural and synthetic water-insoluble resins, it has also been found that there may be employed instead other water-insoluble, water-permeable colloids, for instance cellulose acetate and other cellulose derivatives.
I claim:
1. A self-developable photographic emulsion, comprising a gelatino-silver halide emulsion layer containing from about 3 to 15 grams per liter of emulsion of a photographic developing agent and having a substantially waterinsoluble resin dispersed therein, and having a pH of less than about 6.5.
2. A self-developable photographic emulsion, comprising a gelatino-silver halide emulsion layer containing at least 6 grams per liter of emulsion of a photographic developing agent and having at least 12 grams per liter of emulsion of a substantially water-insoluble resin dispersed therein, and having a pH of less than about 6.5.
3. A sensitive photographic material comprising a paper support having thereon a resinous substratum over which there is a layer of a silver salt emulsion in which has been incorporated a photographic developing agent and a substantially water-insoluble resin such that the pH of the layer is less than about 6.5.
4. The method of producing a self-developable sensitive photographic material which comprises incorporating in a sensitive silver salt emulsion whose pH has been adjusted to below 7, a developing agent and a substantially water-insoluble resin so that the pH is between 5 and 6.5 and then coating such emulsion on a support and drying.
5. A self-d'evelopable photographic material comprising a support bearing a layer comprising a sensitive gelatino-silver bromide emulsion containing a substantially water-insoluble resin selected from the group consisting of soft lac rcsins and glyptal resins, and hydroquinone such that 8 liters of emulsion contain about 50 grams of hydroquinone and about grams of the resin.
EDWARD BOWES KNO'I'I.
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB2315966X | 1940-04-15 | ||
| GB678140A GB549956A (en) | 1941-05-14 | 1941-05-14 | Improvements relating to self-developable photographic materials |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US2315966A true US2315966A (en) | 1943-04-06 |
Family
ID=32095168
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US387446A Expired - Lifetime US2315966A (en) | 1940-04-15 | 1941-04-08 | Photographic emulsion |
Country Status (1)
| Country | Link |
|---|---|
| US (1) | US2315966A (en) |
Cited By (32)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2449153A (en) * | 1944-04-03 | 1948-09-14 | Urbach Franz | Photographic silver bromide emulsion sensitized with cysteine |
| US2478400A (en) * | 1945-08-17 | 1949-08-09 | Eastman Kodak Co | Silver halide photographic emulsion with developer and color coupler dispersed therein |
| US2495000A (en) * | 1945-02-24 | 1950-01-17 | Gen Aniline & Film Corp | Production of azo dyestuff images from n-acyl-n-aryl hydrazine developers |
| US2500421A (en) * | 1944-11-03 | 1950-03-14 | Polaroid Corp | Photographic silver halide transfer process |
| US2525720A (en) * | 1947-01-09 | 1950-10-10 | Polaroid Corp | Photographic product |
| US2563342A (en) * | 1947-01-28 | 1951-08-07 | Polaroid Corp | Photographic product and process |
| US2565376A (en) * | 1947-02-19 | 1951-08-21 | Polaroid Corp | Photographic positive-producing light sensitive element and process |
| US2584030A (en) * | 1947-02-07 | 1952-01-29 | Polaroid Corp | Light sensitive silver halide photographic product for image transfer and process utilizing the same |
| US2592368A (en) * | 1947-11-04 | 1952-04-08 | Eastman Kodak Co | Gelatine silver halide emulsion layer containing a dihydroxy diphenyl tanning developing agent |
| US2600996A (en) * | 1946-10-08 | 1952-06-17 | Polaroid Corp | Photographic product comprising a light-sensitive diazonium compound, a coupler and a rupturable containing means holding ammonia under pressure |
| US2603565A (en) * | 1947-01-15 | 1952-07-15 | Polaroid Corp | Photographic film forming image transfer composition |
| US2607685A (en) * | 1946-10-03 | 1952-08-19 | Polaroid Corp | Photographic product comprising a plurality of rupturable containers, each carrying a liquid for processing said product |
| US2616804A (en) * | 1945-08-13 | 1952-11-04 | Polaroid Corp | Sheet material containing a liquid for processing a silver halide layer |
| US2616805A (en) * | 1946-02-21 | 1952-11-04 | Polaroid Corp | Photographic film assembly comprising a photosensitive layer and another layer hingedly connected together |
| US2616807A (en) * | 1946-11-29 | 1952-11-04 | Polaroid Corp | Silver halide developer containing a film-forming plastic and a water insoluble finely comminuted solid substance |
| US2634886A (en) * | 1946-03-07 | 1953-04-14 | Polaroid Corp | Collapsible fluid container |
| US2639233A (en) * | 1944-06-09 | 1953-05-19 | Polaroid Corp | Photographic product for forming a transfer image |
| US2644756A (en) * | 1947-02-08 | 1953-07-07 | Polaroid Corp | Photographic process for forming a positive transfer image |
| US2647049A (en) * | 1947-02-25 | 1953-07-28 | Polaroid Corp | Photographic element for color photography and a process of producing multicolor pictures |
| US2647055A (en) * | 1946-11-06 | 1953-07-28 | Polaroid Corp | Photographic product and process for forming a white image viewable against a dark background |
| US2653872A (en) * | 1947-01-28 | 1953-09-29 | Polaroid Corp | Photographic product comprising a rupturable container carrying a liquid for processing said product |
| US2661292A (en) * | 1947-02-19 | 1953-12-01 | Polaroid Corp | Product for dispensing a liquidcoated sheet |
| US2661293A (en) * | 1946-10-08 | 1953-12-01 | Polaroid Corp | Process of producing a colored photographic image by means of exhaustion of developer |
| US2687072A (en) * | 1950-02-27 | 1954-08-24 | George A Lohr | Photographic lettering device |
| US2698245A (en) * | 1946-04-13 | 1954-12-28 | Polaroid Corp | Photographic product and process for making a positive transfer image |
| US2698238A (en) * | 1947-02-08 | 1954-12-28 | Polaroid Corp | Photographic product and process |
| US2716059A (en) * | 1952-01-21 | 1955-08-23 | Eastman Kodak Co | Photographic transfer process |
| US2774668A (en) * | 1953-05-28 | 1956-12-18 | Polaroid Corp | Process and product for forming color images from complete dyes |
| US2992102A (en) * | 1955-03-29 | 1961-07-11 | Polaroid Corp | Photographic processes and products |
| US3379529A (en) * | 1963-02-28 | 1968-04-23 | Eastman Kodak Co | Photographic inhibitor-releasing developers |
| US3518088A (en) * | 1965-12-17 | 1970-06-30 | Eastman Kodak Co | Developing agent dispersions |
| US4262086A (en) * | 1978-06-22 | 1981-04-14 | F. F. D., Inc. | Photograph developing solution |
-
1941
- 1941-04-08 US US387446A patent/US2315966A/en not_active Expired - Lifetime
Cited By (32)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2449153A (en) * | 1944-04-03 | 1948-09-14 | Urbach Franz | Photographic silver bromide emulsion sensitized with cysteine |
| US2639233A (en) * | 1944-06-09 | 1953-05-19 | Polaroid Corp | Photographic product for forming a transfer image |
| US2500421A (en) * | 1944-11-03 | 1950-03-14 | Polaroid Corp | Photographic silver halide transfer process |
| US2495000A (en) * | 1945-02-24 | 1950-01-17 | Gen Aniline & Film Corp | Production of azo dyestuff images from n-acyl-n-aryl hydrazine developers |
| US2616804A (en) * | 1945-08-13 | 1952-11-04 | Polaroid Corp | Sheet material containing a liquid for processing a silver halide layer |
| US2478400A (en) * | 1945-08-17 | 1949-08-09 | Eastman Kodak Co | Silver halide photographic emulsion with developer and color coupler dispersed therein |
| US2616805A (en) * | 1946-02-21 | 1952-11-04 | Polaroid Corp | Photographic film assembly comprising a photosensitive layer and another layer hingedly connected together |
| US2634886A (en) * | 1946-03-07 | 1953-04-14 | Polaroid Corp | Collapsible fluid container |
| US2698245A (en) * | 1946-04-13 | 1954-12-28 | Polaroid Corp | Photographic product and process for making a positive transfer image |
| US2607685A (en) * | 1946-10-03 | 1952-08-19 | Polaroid Corp | Photographic product comprising a plurality of rupturable containers, each carrying a liquid for processing said product |
| US2600996A (en) * | 1946-10-08 | 1952-06-17 | Polaroid Corp | Photographic product comprising a light-sensitive diazonium compound, a coupler and a rupturable containing means holding ammonia under pressure |
| US2661293A (en) * | 1946-10-08 | 1953-12-01 | Polaroid Corp | Process of producing a colored photographic image by means of exhaustion of developer |
| US2647055A (en) * | 1946-11-06 | 1953-07-28 | Polaroid Corp | Photographic product and process for forming a white image viewable against a dark background |
| US2616807A (en) * | 1946-11-29 | 1952-11-04 | Polaroid Corp | Silver halide developer containing a film-forming plastic and a water insoluble finely comminuted solid substance |
| US2525720A (en) * | 1947-01-09 | 1950-10-10 | Polaroid Corp | Photographic product |
| US2603565A (en) * | 1947-01-15 | 1952-07-15 | Polaroid Corp | Photographic film forming image transfer composition |
| US2563342A (en) * | 1947-01-28 | 1951-08-07 | Polaroid Corp | Photographic product and process |
| US2653872A (en) * | 1947-01-28 | 1953-09-29 | Polaroid Corp | Photographic product comprising a rupturable container carrying a liquid for processing said product |
| US2584030A (en) * | 1947-02-07 | 1952-01-29 | Polaroid Corp | Light sensitive silver halide photographic product for image transfer and process utilizing the same |
| US2644756A (en) * | 1947-02-08 | 1953-07-07 | Polaroid Corp | Photographic process for forming a positive transfer image |
| US2698238A (en) * | 1947-02-08 | 1954-12-28 | Polaroid Corp | Photographic product and process |
| US2565376A (en) * | 1947-02-19 | 1951-08-21 | Polaroid Corp | Photographic positive-producing light sensitive element and process |
| US2661292A (en) * | 1947-02-19 | 1953-12-01 | Polaroid Corp | Product for dispensing a liquidcoated sheet |
| US2647049A (en) * | 1947-02-25 | 1953-07-28 | Polaroid Corp | Photographic element for color photography and a process of producing multicolor pictures |
| US2592368A (en) * | 1947-11-04 | 1952-04-08 | Eastman Kodak Co | Gelatine silver halide emulsion layer containing a dihydroxy diphenyl tanning developing agent |
| US2687072A (en) * | 1950-02-27 | 1954-08-24 | George A Lohr | Photographic lettering device |
| US2716059A (en) * | 1952-01-21 | 1955-08-23 | Eastman Kodak Co | Photographic transfer process |
| US2774668A (en) * | 1953-05-28 | 1956-12-18 | Polaroid Corp | Process and product for forming color images from complete dyes |
| US2992102A (en) * | 1955-03-29 | 1961-07-11 | Polaroid Corp | Photographic processes and products |
| US3379529A (en) * | 1963-02-28 | 1968-04-23 | Eastman Kodak Co | Photographic inhibitor-releasing developers |
| US3518088A (en) * | 1965-12-17 | 1970-06-30 | Eastman Kodak Co | Developing agent dispersions |
| US4262086A (en) * | 1978-06-22 | 1981-04-14 | F. F. D., Inc. | Photograph developing solution |
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