US1990800A - Photographic developer - Google Patents
Photographic developer Download PDFInfo
- Publication number
- US1990800A US1990800A US626203A US62620332A US1990800A US 1990800 A US1990800 A US 1990800A US 626203 A US626203 A US 626203A US 62620332 A US62620332 A US 62620332A US 1990800 A US1990800 A US 1990800A
- Authority
- US
- United States
- Prior art keywords
- borax
- compounds
- boron
- alkali
- caustic
- 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
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- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 51
- 239000003513 alkali Substances 0.000 description 28
- 229910021538 borax Inorganic materials 0.000 description 24
- 239000004328 sodium tetraborate Substances 0.000 description 24
- 235000010339 sodium tetraborate Nutrition 0.000 description 24
- 150000001875 compounds Chemical class 0.000 description 20
- 235000011121 sodium hydroxide Nutrition 0.000 description 17
- ZOXJGFHDIHLPTG-UHFFFAOYSA-N Boron Chemical compound [B] ZOXJGFHDIHLPTG-UHFFFAOYSA-N 0.000 description 12
- 239000002253 acid Substances 0.000 description 12
- 229910052796 boron Inorganic materials 0.000 description 12
- 239000003518 caustics Substances 0.000 description 12
- 239000003795 chemical substances by application Substances 0.000 description 12
- 239000000126 substance Substances 0.000 description 11
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 9
- KGBXLFKZBHKPEV-UHFFFAOYSA-N boric acid Chemical compound OB(O)O KGBXLFKZBHKPEV-UHFFFAOYSA-N 0.000 description 9
- 235000010338 boric acid Nutrition 0.000 description 8
- 229960002645 boric acid Drugs 0.000 description 8
- 150000001639 boron compounds Chemical class 0.000 description 8
- 239000004327 boric acid Substances 0.000 description 7
- WMFOQBRAJBCJND-UHFFFAOYSA-M Lithium hydroxide Chemical compound [Li+].[OH-] WMFOQBRAJBCJND-UHFFFAOYSA-M 0.000 description 6
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 6
- 239000001301 oxygen Substances 0.000 description 6
- 229910052760 oxygen Inorganic materials 0.000 description 6
- 150000003839 salts Chemical class 0.000 description 6
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 4
- IOLCXVTUBQKXJR-UHFFFAOYSA-M potassium bromide Chemical compound [K+].[Br-] IOLCXVTUBQKXJR-UHFFFAOYSA-M 0.000 description 4
- 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 3
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 3
- 150000007513 acids Chemical class 0.000 description 3
- 150000001447 alkali salts Chemical class 0.000 description 3
- 239000007789 gas Substances 0.000 description 3
- 239000000203 mixture Substances 0.000 description 3
- 150000002926 oxygen Chemical class 0.000 description 3
- 235000011118 potassium hydroxide Nutrition 0.000 description 3
- 239000011734 sodium Substances 0.000 description 3
- 229910052708 sodium Inorganic materials 0.000 description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 3
- VHUUQVKOLVNVRT-UHFFFAOYSA-N Ammonium hydroxide Chemical compound [NH4+].[OH-] VHUUQVKOLVNVRT-UHFFFAOYSA-N 0.000 description 2
- BTBUEUYNUDRHOZ-UHFFFAOYSA-N Borate Chemical compound [O-]B([O-])[O-] BTBUEUYNUDRHOZ-UHFFFAOYSA-N 0.000 description 2
- BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate Chemical compound [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 0.000 description 2
- QIGBRXMKCJKVMJ-UHFFFAOYSA-N Hydroquinone Chemical compound OC1=CC=C(O)C=C1 QIGBRXMKCJKVMJ-UHFFFAOYSA-N 0.000 description 2
- 239000000908 ammonium hydroxide Substances 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- 239000001569 carbon dioxide Substances 0.000 description 2
- 229910002092 carbon dioxide Inorganic materials 0.000 description 2
- 239000000839 emulsion Substances 0.000 description 2
- 230000003993 interaction Effects 0.000 description 2
- BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Chemical compound [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 description 2
- 229940093932 potassium hydroxide Drugs 0.000 description 2
- 239000010802 sludge Substances 0.000 description 2
- 159000000000 sodium salts Chemical class 0.000 description 2
- 239000007787 solid Substances 0.000 description 2
- 239000000243 solution Substances 0.000 description 2
- HDGMAACKJSBLMW-UHFFFAOYSA-N 4-amino-2-methylphenol Chemical compound CC1=CC(N)=CC=C1O HDGMAACKJSBLMW-UHFFFAOYSA-N 0.000 description 1
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 description 1
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 description 1
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 1
- LSNNMFCWUKXFEE-UHFFFAOYSA-N Sulfurous acid Chemical compound OS(O)=O LSNNMFCWUKXFEE-UHFFFAOYSA-N 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 125000004429 atom Chemical group 0.000 description 1
- 239000002585 base Substances 0.000 description 1
- 230000009286 beneficial effect Effects 0.000 description 1
- 150000001638 boron Chemical class 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 230000003247 decreasing effect Effects 0.000 description 1
- UQGFMSUEHSUPRD-UHFFFAOYSA-N disodium;3,7-dioxido-2,4,6,8,9-pentaoxa-1,3,5,7-tetraborabicyclo[3.3.1]nonane Chemical compound [Na+].[Na+].O1B([O-])OB2OB([O-])OB1O2 UQGFMSUEHSUPRD-UHFFFAOYSA-N 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 1
- 125000002768 hydroxyalkyl group Chemical group 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 239000011591 potassium Substances 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- 229910000027 potassium carbonate Inorganic materials 0.000 description 1
- 235000011181 potassium carbonates Nutrition 0.000 description 1
- JVUYWILPYBCNNG-UHFFFAOYSA-N potassium;oxido(oxo)borane Chemical compound [K+].[O-]B=O JVUYWILPYBCNNG-UHFFFAOYSA-N 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- RBWOKKSOBWYZQH-UHFFFAOYSA-N s-octyl benzenecarbothioate Chemical compound CCCCCCCCSC(=O)C1=CC=CC=C1 RBWOKKSOBWYZQH-UHFFFAOYSA-N 0.000 description 1
- 229910000029 sodium carbonate Inorganic materials 0.000 description 1
- 235000017550 sodium carbonate Nutrition 0.000 description 1
- NVIFVTYDZMXWGX-UHFFFAOYSA-N sodium metaborate Chemical compound [Na+].[O-]B=O NVIFVTYDZMXWGX-UHFFFAOYSA-N 0.000 description 1
- 239000001488 sodium phosphate Substances 0.000 description 1
- RYFMWSXOAZQYPI-UHFFFAOYSA-K trisodium phosphate Chemical compound [Na+].[Na+].[Na+].[O-]P([O-])([O-])=O RYFMWSXOAZQYPI-UHFFFAOYSA-K 0.000 description 1
- 229910000406 trisodium phosphate Inorganic materials 0.000 description 1
- 235000019801 trisodium phosphate Nutrition 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
- G03C5/00—Photographic processes or agents therefor; Regeneration of such processing agents
- G03C5/26—Processes using silver-salt-containing photosensitive materials or agents therefor
- G03C5/29—Development processes or agents therefor
- G03C5/305—Additives other than developers
Definitions
- Borax and boric acid have been used in developers of various kinds for some years. In most of the formulae thus far proposed, however, the amount of borax or boric acid has been rela-;' tively small and in most cases where borax was used no other alkali was present. It is, of course, well known that borax has an alkaline reaction. In most of these prior formula, for example,
- borax was used ata concentration of less than 10 grams per liter.
- the substances which I use for the preparation of these alkalies in dry form are, first, a substance containing the radical of one of the oxygen acids of boron and, second, a strong alkali.
- borax or boric acid are particularly useful.
- the second group useful substances are caustic soda (sodium hydroxide), caustic potash (potassiumhydroxide), ammonium hydroxide, lithium hydroxide, sodium carbonate, potassium carbonate, and tri-sodium phosphate.
- Compounds or mixtures of compounds varying in alkalinity from the alkalinity of born to that of caustic soda itself may be prepared by the addition of caustic soda to a solution ofborax.
- caustic soda For example, grams of borax and 50 grams of caustic soda are dissolved in '75 cc. of hot water. on cooling, a white crystalline solid sepa rates which, dried in air free from carbon dioxide, is not as deliquescent as caustic soda, andis very 0 etc.
- caustic soda grams are required for one gram of borax. I prepared with quantities of caustic varying from 0.1 gram to 1.0 gram per gram of borax. Similar compounds may be prepared by the addition of diflerent quantities of caustic soda to boric acid. Other alkalies such as potassium hydroxide, lithium hydroxide or ammonium hydroxide may be substituted for sodium hydroxide or caustic soda in most cases.
- the substance containing the radical of one of the oxy gen acids of boron and the strong alkali may be added separately.
- the following formula is analogous to the formula above but contains the substances separately instead of the compound:
- the compounds of the type I have described prepared by the addition of strong alkali to a,suitable boron compound exert bufiering action on the alkalinity of the developer, that is, they tend to maintain the solution at a fixed degree of alkalinity.
- This characteristic is in itself a valuable advantage-
- a further advantage in the use of developers such as I have described is that they reduce the possibility of ,blisters forming on photographic prints and films during the usual processing steps. As is well understood, blisters are likely to be formed when aphotographic print, for example,
- a photographic developer comprising a developing agent, a sulflte, and a metaborate.
- a photographic developer comprising-a silver-halide developing agent, a sulfite and a chemical product selected from the products resulting fromthe interaction of sodium hydroxide and borax where the proportion of sodium hydroxide to borax lies between one tenth and unity.
- a photographic developer comprising a silver-halide developing agent and potassium metaborate.
- a photographic developer comprising a developing agent and ammonium metaborate.
- a photographic developer comprising a silyer-halide developing agent, an alkaline-reacting salt of an oxygen acid of boron, a caustic alkali, the proportion of the alkaline-reacting salt of an oxygen acid of boron'to the caustic alkali being between 1:1 and 10:1.
- a photographic developer comprising a silver-halide developing agent, an alkaline-reacting salt of an oxygen acid of boron, a caustic alkali, the proportionof the alkaline-reacting salt of an oxygen acid of boron to the caustic alkali being between 1:1 and .10:1, said alkaline-reacting a metaborate.
- a photographic developer comprising a siling salt of an oxygen acid of boron, and a caustic ver-halide developing agent and a metaborate. alkali, the proportion of the alkaline-reacting salt 9.
- a photographic developer comprising a silof an oxygen acid of boron to the caustic alkali ver-halide developing agent and. an alkali meta- ,being approximately 2:1;
- a photographic developer comprising a sil- 5 10.
- a photographic developer comprising a ver-halide developing agent, borax, and a caustic silver-halide developing agent and an alkali metaalkali, the proportion of the borax to the caustic borate, in aqueous solution. alkali being approximately 2:1.
- a photographic developer comprising a 1Q silver-halide developing agent; an alkaline-react- HAROLD D. RUSSELL. 10
Landscapes
- Physics & Mathematics (AREA)
- General Physics & Mathematics (AREA)
- Silver Salt Photography Or Processing Solution Therefor (AREA)
Description
Patented Feb. 12, 1935 1,990,800 rno'roeaarmc naviipom .Harold D. Russell, Rochester, N. Y., allignor to Eastman Kodak Company. Rochester, N. Y a corporation of New York No Drawing. Application July 39, 1982, Serial N0. 626,203
12 Claims. (01. 95-48) F This invention relates to photographic developers and particularly to alkalies for use in developers.
Borax and boric acid have been used in developers of various kinds for some years. In most of the formulae thus far proposed, however, the amount of borax or boric acid has been rela-;' tively small and in most cases where borax was used no other alkali was present. It is, of course, well known that borax has an alkaline reaction. In most of these prior formula, for example,
, borax was used ata concentration of less than 10 grams per liter.
I have found, that excellent developers may be made if much greater concentrations of borax or boric acidare used together with suitable and relatively large amounts of strong alkalies. I have further found that the boron compound and the alkali may be prepared in the form of a dry substance which is a product of the interaction of the alkali ,and the boron compound. Such'a compound in dry form of itself ofiers many advantages. Compounds of any degree of alkalinity ranging from that of borax itself,
which is a relatively weak alkali, to that of caustic 1 soda, for example, may be prepared. These com- 7 pounds will then provide in a single dry harmless substance all the alkali that is needed for any formula. They offer marked advantages in use over 'the stronger alkalies such as caustic soda, particularly in handling. Other advantages will also appear from the following specification.
The substances which I use for the preparation of these alkalies in dry form are, first, a substance containing the radical of one of the oxygen acids of boron and, second, a strong alkali. Of the first group borax or boric acid are particularly useful. Of'the second group useful substances are caustic soda (sodium hydroxide), caustic potash (potassiumhydroxide), ammonium hydroxide, lithium hydroxide, sodium carbonate, potassium carbonate, and tri-sodium phosphate.
A number of oxygen acids of boron are known, the alkali salts ofany of which would be useful for making compounds more alkaline than Various alkali salts of these acids have been described in the literature. with the exception of boric acid (orth'o boric, H4301) and borax (sodium tetraborate, NfiaBiOLl-OHIO), none of these compounds, have found any application in photographic developers.
It will be understood in what follows that the alkali salts of any of these acids are useful in the manner described. Of the sodium salts, I employ only those which are more alkaline than borax. It is also true that in using these substances in various proportions with the alkalies as indicated a large variety and mixtures of compounds may be formed. It is not essential, of course, for the carrying out of my invention to ascertain the definite identity of the compounds present.
Of the various satisfactory acids vof boron any one may be used interchangeably for another,
and each can be evaluated in terms of equivalents of another. Equivalents are calculated on the basis of the boron content. Thus, referring to the preceding list, the following are equivalent weights, based on molecular weights:
Compounds of theacids of boron which are, as satisfactory as any formy purpose are those made from borax and caustic soda and I will illustrate my invention by their use, though not being limited in any way by the particular example given.
Compounds or mixtures of compounds varying in alkalinity from the alkalinity of born to that of caustic soda itself may be prepared by the addition of caustic soda to a solution ofborax. For example, grams of borax and 50 grams of caustic soda are dissolved in '75 cc. of hot water. on cooling, a white crystalline solid sepa rates which, dried in air free from carbon dioxide, is not as deliquescent as caustic soda, andis very 0 etc.
alkaline when dissolved in water. Instead of allowing to crystallize, the mixture may be evaporated to dryness. L
Similar substances may be preparedby the addition of more or less caustic soda. For the formation of the sodium salt of ortho boric acid (H3303) which contains the greatest number of hydrogen atoms per 'atom of borax. 1.05
grams of caustic soda are required for one gram of borax. I prepared with quantities of caustic varying from 0.1 gram to 1.0 gram per gram of borax. Similar compounds may be prepared by the addition of diflerent quantities of caustic soda to boric acid. Other alkalies such as potassium hydroxide, lithium hydroxide or ammonium hydroxide may be substituted for sodium hydroxide or caustic soda in most cases.
' These compounds may be used as alkalies in White crystalline solids have been photographic developers and as stated, developers with widely varying activities may be prepared with them. The following is an example of a developer containing one oi these compounds. A compound as described is formed from grams. of borax and 50 grams 0! caustic soda. This is then used in the following developer formula:
Monosmethyl p-amino phenol sulfate; 1 gram Hydroqinnone 5 grams Sodium sulflte 50 grams Borax-caustic compoimd 20 grams Potassium bromide 1 gram Wa'Lterto 1 liter As already stated a large number of the borax-caustic compounds can be prepared and they may be used in varying proportions to give developers of quite a wide range in characteristics. The particular one just described is given by way of example only.
Instead of using the dry compounds the substance containing the radical of one of the oxy gen acids of boron and the strong alkali may be added separately. The following formula is analogous to the formula above but contains the substances separately instead of the compound:
Mono-methyl p-amino phenol sulfate- 1 gram Hydroquinone 5 grams Sodium sulflte 50 grams Borax 20 grams Sodium hydroxide 5 grams Potassium bromide 1 gram Water to 1 liter secondary bases, and the hydroxy alkyl substituted amines such as those described in my copending application Ser. No. 590,517 flled Febru-' ary 2, 1932, and that of M. L. Dundon Ser. No. 590,520 filed February 2,1932, which has niatured into Patent1,925,55'7, granted Sept. 5, 1933. It is to be pointed out that the compounds of the type I have described prepared by the addition of strong alkali to a,suitable boron compound exert bufiering action on the alkalinity of the developer, that is, they tend to maintain the solution at a fixed degree of alkalinity. This was not true in the prior use of borax or boric acid in developers where the concentration of borax, for example, was relatively low with a concentration of another alkali. This characteristic is in itself a valuable advantage- A further advantage in the use of developers such as I have described is that they reduce the possibility of ,blisters forming on photographic prints and films during the usual processing steps. As is well understood, blisters are likely to be formed when aphotographic print, for example,
is developed in a. developer containing a soluble carbonate and is then passed over into an acid fixing'bath. A certain amount of the carbonate is carried over with the print and on reaction with the acid of the fixing bath forms carbon dioxide gas (002). A certain amount of this I bonates.
Developers containing the compounds described or, larger amounts of the boron compounds and gas may become entran emul sion and as it expands mi its formation win form Most or the compounds of the type a blister. described do not liberate CO: or any other gas and the tendency to blister is thereby eliminated. The only. compoundswhich might liberate C0:
are those made with sodium or potassium carthe alkalies separately also have another advantage which has only recently been discovered. In the copending application, Serial No. 588,502, filed January 22, 1932 by R. S. Becker is described a. fixing hardening bath containing boric acid and the acetate ion. It was found that-such fixing baths show greatly increased hardening life and a greatly decreased tendencyto sludge. It has now been found that the small amounts of the boron compounds which are carried over from developers of the kind here under consideration by films and'prints into the fixing bath are also suflicient to exert this very beneficial influence on the hardening life and 'sludging properties. In other words, prints or films developed in developers containing larger amounts-of the boron compounds as indicated, briefly rinsed, and then placed in the usual type of acid hardening bath carry over in the emulsion sufilcient of the boron compounds to materially increase the.
hardening life of the bath and-to decrease the tendency to sludge. This in itself is an important tion is possible not only in the making of the compounds between the substances containing the radical of the boron acids and the alkalies but also in the formula: of developers containing them or the boron compounds and alkalies separately.
I consider as included in my invention .a variations and modifications coming within the scope of the appended claims.
What I claim is: I
1. A photographic developer comprising a developing agent, a sulflte, and a metaborate.
2. A photographic developer comprising-a silver-halide developing agent, a sulfite and a chemical product selected from the products resulting fromthe interaction of sodium hydroxide and borax where the proportion of sodium hydroxide to borax lies between one tenth and unity.
3. A photographic developer'comprisinga silver-halide developing agent and sodium metaborate.
4. A photographic developer comprising a silver-halide developing agent and potassium metaborate.
5. A photographic developer comprising a developing agent and ammonium metaborate.
6. A photographic developer comprising a silyer-halide developing agent, an alkaline-reacting salt of an oxygen acid of boron, a caustic alkali, the proportion of the alkaline-reacting salt of an oxygen acid of boron'to the caustic alkali being between 1:1 and 10:1.
'7. A photographic developer comprising a silver-halide developing agent, an alkaline-reacting salt of an oxygen acid of boron, a caustic alkali, the proportionof the alkaline-reacting salt of an oxygen acid of boron to the caustic alkali being between 1:1 and .10:1, said alkaline-reacting a metaborate.
1,'cao,soo 3' 8. A photographic developer comprising a siling salt of an oxygen acid of boron, and a caustic ver-halide developing agent and a metaborate. alkali, the proportion of the alkaline-reacting salt 9. A photographic developer comprising a silof an oxygen acid of boron to the caustic alkali ver-halide developing agent and. an alkali meta- ,being approximately 2:1;
5 borate. 12. A photographic developer comprising a sil- 5 10. A photographic developer comprising a ver-halide developing agent, borax, and a caustic silver-halide developing agent and an alkali metaalkali, the proportion of the borax to the caustic borate, in aqueous solution. alkali being approximately 2:1.
11. A photographic developer comprising a 1Q silver-halide developing agent; an alkaline-react- HAROLD D. RUSSELL. 10
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US626203A US1990800A (en) | 1932-07-29 | 1932-07-29 | Photographic developer |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US626203A US1990800A (en) | 1932-07-29 | 1932-07-29 | Photographic developer |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US1990800A true US1990800A (en) | 1935-02-12 |
Family
ID=24509392
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US626203A Expired - Lifetime US1990800A (en) | 1932-07-29 | 1932-07-29 | Photographic developer |
Country Status (1)
| Country | Link |
|---|---|
| US (1) | US1990800A (en) |
Cited By (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2657137A (en) * | 1947-07-14 | 1953-10-27 | Grinten Chem L V D | Developer for the positive diazotype-process containing a borate, a polyhydroxy alcohol, and a coupler component |
| US2706157A (en) * | 1951-07-21 | 1955-04-12 | Grant Photo Products Inc | Processing photographic paper and film |
| US2825647A (en) * | 1954-10-28 | 1958-03-04 | Robert E Fuller | Photographic developer |
| FR2408855A1 (en) * | 1977-11-09 | 1979-06-08 | Polaroid Corp | NEW PHOTOGRAPHIC TREATMENT COMPOSITION |
-
1932
- 1932-07-29 US US626203A patent/US1990800A/en not_active Expired - Lifetime
Cited By (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2657137A (en) * | 1947-07-14 | 1953-10-27 | Grinten Chem L V D | Developer for the positive diazotype-process containing a borate, a polyhydroxy alcohol, and a coupler component |
| US2706157A (en) * | 1951-07-21 | 1955-04-12 | Grant Photo Products Inc | Processing photographic paper and film |
| US2825647A (en) * | 1954-10-28 | 1958-03-04 | Robert E Fuller | Photographic developer |
| FR2408855A1 (en) * | 1977-11-09 | 1979-06-08 | Polaroid Corp | NEW PHOTOGRAPHIC TREATMENT COMPOSITION |
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