US2983609A - Chemical sensitization of photographic emulsions - Google Patents
Chemical sensitization of photographic emulsions Download PDFInfo
- Publication number
- US2983609A US2983609A US629459A US62945956A US2983609A US 2983609 A US2983609 A US 2983609A US 629459 A US629459 A US 629459A US 62945956 A US62945956 A US 62945956A US 2983609 A US2983609 A US 2983609A
- Authority
- US
- United States
- Prior art keywords
- silver halide
- emulsions
- sulfinic acid
- formamidine sulfinic
- photographic silver
- 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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- 239000000839 emulsion Substances 0.000 title claims description 60
- 206010070834 Sensitisation Diseases 0.000 title description 5
- 230000008313 sensitization Effects 0.000 title description 5
- 239000000126 substance Substances 0.000 title description 4
- -1 SILVER HALIDE Chemical class 0.000 claims description 37
- 229910052709 silver Inorganic materials 0.000 claims description 34
- 239000004332 silver Substances 0.000 claims description 34
- NYYSPVRERVXMLJ-UHFFFAOYSA-N 4,4-difluorocyclohexan-1-one Chemical compound FC1(F)CCC(=O)CC1 NYYSPVRERVXMLJ-UHFFFAOYSA-N 0.000 claims description 24
- 230000001235 sensitizing effect Effects 0.000 claims description 15
- 230000035945 sensitivity Effects 0.000 description 13
- 239000000975 dye Substances 0.000 description 11
- 239000000463 material Substances 0.000 description 9
- 238000000034 method Methods 0.000 description 9
- 238000000576 coating method Methods 0.000 description 7
- 230000001965 increasing effect Effects 0.000 description 7
- 150000001875 compounds Chemical class 0.000 description 6
- 239000010410 layer Substances 0.000 description 6
- 230000029087 digestion Effects 0.000 description 5
- 230000003287 optical effect Effects 0.000 description 5
- 239000002253 acid Substances 0.000 description 4
- 239000011248 coating agent Substances 0.000 description 4
- 230000005070 ripening Effects 0.000 description 4
- 230000003595 spectral effect Effects 0.000 description 4
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 3
- 229920000159 gelatin Polymers 0.000 description 3
- 239000008273 gelatin Substances 0.000 description 3
- 238000010348 incorporation Methods 0.000 description 3
- 229910052700 potassium Inorganic materials 0.000 description 3
- 239000011591 potassium Substances 0.000 description 3
- 150000003455 sulfinic acids Chemical class 0.000 description 3
- RYYXDZDBXNUPOG-UHFFFAOYSA-N 4,5,6,7-tetrahydro-1,3-benzothiazole-2,6-diamine;dihydrochloride Chemical compound Cl.Cl.C1C(N)CCC2=C1SC(N)=N2 RYYXDZDBXNUPOG-UHFFFAOYSA-N 0.000 description 2
- 108010010803 Gelatin Proteins 0.000 description 2
- 229910052783 alkali metal Inorganic materials 0.000 description 2
- 239000000084 colloidal system Substances 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 235000019322 gelatine Nutrition 0.000 description 2
- 235000011852 gelatine desserts Nutrition 0.000 description 2
- 238000002360 preparation method Methods 0.000 description 2
- 150000003839 salts Chemical class 0.000 description 2
- 230000006641 stabilisation Effects 0.000 description 2
- 238000011105 stabilization Methods 0.000 description 2
- PNKUSGQVOMIXLU-UHFFFAOYSA-N Formamidine Chemical compound NC=N PNKUSGQVOMIXLU-UHFFFAOYSA-N 0.000 description 1
- 206010067482 No adverse event Diseases 0.000 description 1
- 229910021607 Silver chloride Inorganic materials 0.000 description 1
- 239000006096 absorbing agent Substances 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 230000002411 adverse Effects 0.000 description 1
- 125000004429 atom Chemical group 0.000 description 1
- 230000006399 behavior Effects 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- 239000000298 carbocyanine 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
- 230000015271 coagulation Effects 0.000 description 1
- 238000005345 coagulation Methods 0.000 description 1
- 230000008878 coupling Effects 0.000 description 1
- 238000010168 coupling process Methods 0.000 description 1
- 238000005859 coupling reaction Methods 0.000 description 1
- 239000002270 dispersing agent Substances 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 238000004945 emulsification Methods 0.000 description 1
- 230000002708 enhancing effect Effects 0.000 description 1
- RQIFXTOWUNAUJC-UHFFFAOYSA-N ethanesulfinic acid Chemical compound CCS(O)=O RQIFXTOWUNAUJC-UHFFFAOYSA-N 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 150000002343 gold Chemical class 0.000 description 1
- PCHJSUWPFVWCPO-UHFFFAOYSA-N gold Chemical compound [Au] PCHJSUWPFVWCPO-UHFFFAOYSA-N 0.000 description 1
- 239000010931 gold Substances 0.000 description 1
- 229910052737 gold Inorganic materials 0.000 description 1
- 150000002344 gold compounds Chemical class 0.000 description 1
- RJHLTVSLYWWTEF-UHFFFAOYSA-K gold trichloride Chemical compound Cl[Au](Cl)Cl RJHLTVSLYWWTEF-UHFFFAOYSA-K 0.000 description 1
- 125000000623 heterocyclic group Chemical group 0.000 description 1
- 239000011229 interlayer Substances 0.000 description 1
- DZVCFNFOPIZQKX-LTHRDKTGSA-M merocyanine Chemical compound [Na+].O=C1N(CCCC)C(=O)N(CCCC)C(=O)C1=C\C=C\C=C/1N(CCCS([O-])(=O)=O)C2=CC=CC=C2O\1 DZVCFNFOPIZQKX-LTHRDKTGSA-M 0.000 description 1
- XNEFVTBPCXGIRX-UHFFFAOYSA-N methanesulfinic acid Chemical compound CS(O)=O XNEFVTBPCXGIRX-UHFFFAOYSA-N 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 125000004433 nitrogen atom Chemical group N* 0.000 description 1
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N phenol group Chemical group C1(=CC=CC=C1)O ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 1
- 229920000915 polyvinyl chloride Polymers 0.000 description 1
- JEXVQSWXXUJEMA-UHFFFAOYSA-N pyrazol-3-one Chemical compound O=C1C=CN=N1 JEXVQSWXXUJEMA-UHFFFAOYSA-N 0.000 description 1
- 239000001397 quillaja saponaria molina bark Substances 0.000 description 1
- 229930182490 saponin Natural products 0.000 description 1
- 150000007949 saponins Chemical class 0.000 description 1
- 238000001228 spectrum Methods 0.000 description 1
- 238000006467 substitution reaction Methods 0.000 description 1
- BUUPQKDIAURBJP-UHFFFAOYSA-N sulfinic acid Chemical compound OS=O BUUPQKDIAURBJP-UHFFFAOYSA-N 0.000 description 1
- 229920003002 synthetic resin Polymers 0.000 description 1
- 239000000057 synthetic resin Substances 0.000 description 1
- ANRHNWWPFJCPAZ-UHFFFAOYSA-M thionine Chemical compound [Cl-].C1=CC(N)=CC2=[S+]C3=CC(N)=CC=C3N=C21 ANRHNWWPFJCPAZ-UHFFFAOYSA-M 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 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
- G03C1/08—Sensitivity-increasing substances
- G03C1/09—Noble metals or mercury; Salts or compounds thereof; Sulfur, selenium or tellurium, or compounds thereof, e.g. for chemical sensitising
Definitions
- This invention relates to photographic silver halide emulsions, and more particularly, to a means for chemically sensitizing such photographic silver halide emulsions.
- an object of our invention to provide photographic silver halide emulsions which have been chemically sensitized. Another object is to provide a method of preparing such sensitized emulsions. Still another object of our invention is to provide photographic silver halide emulsions which have increased sensitivity, without concomitant increases in log, or poor keeping qualities, to a degree which might seriously affect the usefulness of the sensitized emulsions. Other objects will become apparent from a consideration of the following description and examples.
- Formamidine sulfinic acid is sometimes known as thiourea dioxide, depending upon the particular tautomeric form in which the compound is written.
- Formamidine sulfinic acid (or thiourea dioxide) can be represented as existing in the following state of equilibrium:
- the preparation of silver halide emulsions involves three separate operations: (1) the emulsification and digestion or ripening of the silver halide, (2) the freeing of the emulsion from excess soluble salts, usually by washing, and (3) the second digestion or after-ripening to obtain increased sensitivity. (Mees, The Theory of the Photographic Process, 1942). We prefer to add the sensitizing compound of our invention before the final digestion or after-ripening, although it can also be added after digestion.
- the quantity of formamidine sulfinic acid added to the photographic silver halide emulsions can be varied, depending upon the particular effect desired, degree of ripening, silver halide content of the emulsion, etc. We have found that generally from about 0.05 to about 20 mg. of formamidine sulfinic acid per mole of silver halide is quite satisfactory to accomplish the sensitization of the emulsions. We have further found. that increased sensitization can be obtained, and that larger quantities of formamidine sulfinic acid can be employed, in cases where the final ripening of the silver halide emulsion is carried out for longer periods of time than normal, but at lower ripening temperatures.
- the photographic silver halide emulsions used in practicing our invention are generally of the developing-out type. It is to be understood that the amount of silver halide in the emulsions can be varied, depending upon the particular purpose for which the emulsion is to be employed. Particularly useful results can be obtained when formamidine sulfinic acid is employed in conjunction with gelatino-silver-bromiodide emulsions, although it can also be advantageously employed in sensitizing other silver halide emulsions, such as gelatino-silverchloride, -bromide, -chl0robromide, -chiorobromiodide, etc., emulsions.
- the photographic silver halide emulsions used in practicing our invention can also be optically sensitized by means of the dyes customarily employed in photography, such as cyanine dyes, carbocyanine dyes, dicarbocyanine dyes, merocyanine dyes, holopolar dyes, etc.
- the sensitizing effect obtained in our invention is not completely independent of the optical or spectral sensitizing dyes commonly used, although no adverse effects have been noted in using emulsions which have been optically sensitized.
- the formamidine sulfinic acid of our invention can be employed in conjunction with other chemical sensitizers.
- the photographic silver halide emulsions employed in practicing our invention can also contain antifoggants or materials known to stabilize the emulsions against loss of speed under adverse keeping conditions, such as those customarily encountered in the tropics.
- antifoggants include, for example, those described in Allen et al. U.S. application Serial No. 586,654, filed May 23, 1956, as well as many of the antifoggant compounds which can be generally classed as polyazaindenes.
- polyazaindenes have been described in US. Patents 2,444- 604-9; 2,743,181; 2,735,769; etc.
- the photographic silver halide emulsions employed in our invention can be used in the preparation of materials, such as multilayer materials, intended for use in color photography, where a number of separate silver halide emulsion layers are sensitized for a particular region of the spectrum.
- materials such as multilayer materials, intended for use in color photography, where a number of separate silver halide emulsion layers are sensitized for a particular region of the spectrum.
- multilayer color materials generally have a red-sensitive layer coated on a support,
- These light-sensitive layers can contain color-forming materials of the type customarily employed in color photography, such as coupling compounds containing reactive ketomethylene groups, phenolic groups, or heterocyclic groups, such as pyrazolone. See, for example, US. Patent 2,640,776. These color-forming compounds can be incorporated in water-insoluble, low molecular weight, organic, crystalloidal materials having a boiling point above about 175 C., such materials being. of the type described in US. Patent 2,322,027.
- the chemical sensitizer of our invention is useful in combination with emulsions which have been sensitized with gold salts, such as those described in Waller and Dodd US. Patent 2,399,038, or Damschroder US. Patent 2,597,856 or Yutzy and Leermakers US. Patent 2,597,915 (e.g., potassium chloroaun'te, potassium aurithiocyanate, potassium chloroaurate, auric trichloride, 2-aurosulfobenzothiazole methochloride, etc.). Also, emulsions which have been sulfur-sensitized, such as by the procedures shown in Sheppard US. Patent 1,574,944 or US.
- gold salts such as those described in Waller and Dodd US. Patent 2,399,038, or Damschroder US. Patent 2,597,856 or Yutzy and Leermakers US. Patent 2,597,915 (e.g., potassium chloroaun'te, potassium aurithiocyan
- Patent 1,623,499 or Sheppard and Brigham US. Patent 2,410,689 can be employed in our invention.
- Such sulfur-sensitized emulsions can additionally contain gold sensitizers of the type mentioned above, or gold compounds intended primarily for stabilization purposes.
- Example 1 A fine-grain, low-gelatin, positive speed bromiodide emulsion was prepared and washed by the acid coagulation method described in US. Patent 2,614,928. The pH of the emulsion was then adjusted to 6.0 and the emulsion held for 50 minutes at 60 C., both in the absence and presence of formamidine sulfinic acid. Additional gelatin and a coating aid, such as saponin, were then added and the emulsion coated on a suitable support, such as glass, cellulose acetate film, polyvinyl resin film, etc. After drying, the coatings were exposed for 1/25 second positive on an Eastman Type lb sensitometer and developed for 6 minutes at 70 F. in a developer having the following composition:
- formamidine sulfinic acid of our invention when employing the formamidine sulfinic acid of our invention in alkaline photographic silver halide emulsions, it is to be understood that an alkali metal salt thereof may be formed and that the alkali metal salt exists in ionic form.
- the probability of salt formation under such alkaline conditions is well understood by those skilled in the art and it is to be understood that the reference in the foregoing specification, and in the follow-ing claims, to formamidine sulfinic acid includes the use of such material in acid or alkaline emulsions.
- these photographic emulsions can be sensitized or not, by means of optical sensitizing dyes.
- Such photographic emulsions can be orthochromatic, panchromatic, or X-ray emulsions.
- the formamidine sulfinic acid can be added to the emulsion before or after such dyes are added.
- Suitable dispersing agents for the silver halide emulsions sensitized according to our invention comprise gelatin, or other colloids, such as collodion, albumen, cellulose organic derivatives, synthetic resins, etc.
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- Physics & Mathematics (AREA)
- Chemical & Material Sciences (AREA)
- Spectroscopy & Molecular Physics (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- General Physics & Mathematics (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Description
Unite This invention relates to photographic silver halide emulsions, and more particularly, to a means for chemically sensitizing such photographic silver halide emulsions.
A number of methods have been previously proposed for increasing the sensitivity of photographic silver halide emulsions, other than methods of optical or spectral sensitization which involve the incorporation of certain dyes in the emulsions. in the emulsions increases the optical range of sensitivity, whereas the incorporation of other materials known as chemical sensitizers increases the speed and generally the gamma of the emulsion without materially affecting the optical range of sensitivity. Many of the prior methods of enhancing sensitivity, other than the methods of spectral sensitization, leave much to be desired because the increase of sensitivity may be quite small or the increase in sensitivity is accompanied by excessive fog and/ or excessively poor keeping qualities of the sensitized emulsions.
We have now found a method of increasing the sensitivity of photographic silver halide emulsions wherein the speed increases are quite substantial, while the fog and keeping qualities are not excessively affected, considering the magnitude of the increases in speed and gamma or contrast obtained.
It is, therefore, an object of our invention to provide photographic silver halide emulsions which have been chemically sensitized. Another object is to provide a method of preparing such sensitized emulsions. Still another object of our invention is to provide photographic silver halide emulsions which have increased sensitivity, without concomitant increases in log, or poor keeping qualities, to a degree which might seriously affect the usefulness of the sensitized emulsions. Other objects will become apparent from a consideration of the following description and examples.
According to our invention, We have found that the sensitivity of photographic silver halide emulsions can be materially increased by incorporating formamidine sulfinic acid therein. Formamidine sulfinic acid is sometimes known as thiourea dioxide, depending upon the particular tautomeric form in which the compound is written. Formamidine sulfinic acid (or thiourea dioxide) can be represented as existing in the following state of equilibrium:
It has been previously proposed to incorporate various sulfinic acids in photographic silver halide emulsions for the purpose of increasing the stability thereof. For example, U.S. Patent 2,057,764 suggests the addition of alkane sulfinic acids, such as methane sulfinic acid, ethane sulfinic acid, etc., to photographic silver halide emulsions for the purpose of stabilization. However, as noted in this patent, these sulfinic acids have no detectable eifect upon the sensitivity characteristics of the photographic silver halide emulsions. Contrasted with this behavior, the formamidine sulfinic acid of our invention has a profound effect upon the sensitivity characteristics of the photographic silver halide emulsions. Moreover, we have found that even more closely related acids than States Patent T The incorporation of dyes Patented May 9, 1961 the sulfinic acids of US. Patent 2,057,764 fail to eflFectively increase the sensitivity of photographic silver halide emulsions. For example, various types of substitution on the nitrogen atom or atoms of formamidine sulfinic acid appears to materially decrease or destroy the sensitizing characteristics of the parent compound.
The preparation of silver halide emulsions involves three separate operations: (1) the emulsification and digestion or ripening of the silver halide, (2) the freeing of the emulsion from excess soluble salts, usually by washing, and (3) the second digestion or after-ripening to obtain increased sensitivity. (Mees, The Theory of the Photographic Process, 1942). We prefer to add the sensitizing compound of our invention before the final digestion or after-ripening, although it can also be added after digestion.
The quantity of formamidine sulfinic acid added to the photographic silver halide emulsions can be varied, depending upon the particular effect desired, degree of ripening, silver halide content of the emulsion, etc. We have found that generally from about 0.05 to about 20 mg. of formamidine sulfinic acid per mole of silver halide is quite satisfactory to accomplish the sensitization of the emulsions. We have further found. that increased sensitization can be obtained, and that larger quantities of formamidine sulfinic acid can be employed, in cases where the final ripening of the silver halide emulsion is carried out for longer periods of time than normal, but at lower ripening temperatures.
The photographic silver halide emulsions used in practicing our invention are generally of the developing-out type. It is to be understood that the amount of silver halide in the emulsions can be varied, depending upon the particular purpose for which the emulsion is to be employed. Particularly useful results can be obtained when formamidine sulfinic acid is employed in conjunction with gelatino-silver-bromiodide emulsions, although it can also be advantageously employed in sensitizing other silver halide emulsions, such as gelatino-silverchloride, -bromide, -chl0robromide, -chiorobromiodide, etc., emulsions.
The photographic silver halide emulsions used in practicing our invention can also be optically sensitized by means of the dyes customarily employed in photography, such as cyanine dyes, carbocyanine dyes, dicarbocyanine dyes, merocyanine dyes, holopolar dyes, etc. The sensitizing effect obtained in our invention is not completely independent of the optical or spectral sensitizing dyes commonly used, although no adverse effects have been noted in using emulsions which have been optically sensitized. Also, the formamidine sulfinic acid of our invention can be employed in conjunction with other chemical sensitizers.
The photographic silver halide emulsions employed in practicing our invention can also contain antifoggants or materials known to stabilize the emulsions against loss of speed under adverse keeping conditions, such as those customarily encountered in the tropics. Such antifoggants include, for example, those described in Allen et al. U.S. application Serial No. 586,654, filed May 23, 1956, as well as many of the antifoggant compounds which can be generally classed as polyazaindenes. Such polyazaindenes have been described in US. Patents 2,444- 604-9; 2,743,181; 2,735,769; etc.
The photographic silver halide emulsions employed in our invention can be used in the preparation of materials, such as multilayer materials, intended for use in color photography, where a number of separate silver halide emulsion layers are sensitized for a particular region of the spectrum. Such multilayer color materials generally have a red-sensitive layer coated on a support,
followed by a green-sensitive layer, a blue light-absorb-- i i 3 ing layer, and a blue-sensitive layer, together with one or more interlayers comprisinggelatin or some other colloid having various addenda, such as ultraviolet absorbing agents, etc, incorporated therein. These light-sensitive layers can contain color-forming materials of the type customarily employed in color photography, such as coupling compounds containing reactive ketomethylene groups, phenolic groups, or heterocyclic groups, such as pyrazolone. See, for example, US. Patent 2,640,776. These color-forming compounds can be incorporated in water-insoluble, low molecular weight, organic, crystalloidal materials having a boiling point above about 175 C., such materials being. of the type described in US. Patent 2,322,027.
It has been found that the chemical sensitizer of our invention is useful in combination with emulsions which have been sensitized with gold salts, such as those described in Waller and Dodd US. Patent 2,399,038, or Damschroder US. Patent 2,597,856 or Yutzy and Leermakers US. Patent 2,597,915 (e.g., potassium chloroaun'te, potassium aurithiocyanate, potassium chloroaurate, auric trichloride, 2-aurosulfobenzothiazole methochloride, etc.). Also, emulsions which have been sulfur-sensitized, such as by the procedures shown in Sheppard US. Patent 1,574,944 or US. Patent 1,623,499 or Sheppard and Brigham US. Patent 2,410,689 can be employed in our invention. Such sulfur-sensitized emulsions can additionally contain gold sensitizers of the type mentioned above, or gold compounds intended primarily for stabilization purposes.
The following examples will serve to illustrate more fully the manner of practicing our invention:
. Example 1 A fine-grain, low-gelatin, positive speed bromiodide emulsion was prepared and washed by the acid coagulation method described in US. Patent 2,614,928. The pH of the emulsion was then adjusted to 6.0 and the emulsion held for 50 minutes at 60 C., both in the absence and presence of formamidine sulfinic acid. Additional gelatin and a coating aid, such as saponin, were then added and the emulsion coated on a suitable support, such as glass, cellulose acetate film, polyvinyl resin film, etc. After drying, the coatings were exposed for 1/25 second positive on an Eastman Type lb sensitometer and developed for 6 minutes at 70 F. in a developer having the following composition:
N-methyl-p-aminophenol sulfate 0.3 Hydroquinone 6.0 Sodium sulfite (dry) 38.0 Sodium bisulfite 1.5 Sodium carbonate monohydrate 22.0 Sodium bromide 0.78 Citric acid 0.7
Water to make one liter.
The speed contrast and fog for each of the emulsion coatings was measured, comparison being made between the coating containing no formamidine sulfinic acid, and coatings containing formamidine sulfinic acid in the quantities indicated below (the amount being on the basis of per mole of silver halide present). The results follow:
A fine-grain emulsion prepared in exactly the manner shown in Example 1, except that the final digestion was for 1 hour at 40 C., was treated in the presence and absence of 'formamidine sulfinic acid in the amounts inresults follow:
Formainidine sulfinic acid (mg/mole .AgX)
30/E Gamma Speed Coating Fog tizer was then compared with an identical batch contain-.
ing the sensitizer in the amounts indicated below. Exposure and development was identical to that of Ex: ample l. The results follow:
Formamidine sulfinic acid (mg/mole AgX) Coating 30/E Gamma Fog Speed None (1;) 6. 0
When employing the formamidine sulfinic acid of our invention in alkaline photographic silver halide emulsions, it is to be understood that an alkali metal salt thereof may be formed and that the alkali metal salt exists in ionic form. The probability of salt formation under such alkaline conditions is well understood by those skilled in the art and it is to be understood that the reference in the foregoing specification, and in the follow-ing claims, to formamidine sulfinic acid includes the use of such material in acid or alkaline emulsions. As indicated above, these photographic emulsions can be sensitized or not, by means of optical sensitizing dyes. Such photographic emulsions can be orthochromatic, panchromatic, or X-ray emulsions. If used with spectral sensitizing dyes, the formamidine sulfinic acid can be added to the emulsion before or after such dyes are added. Suitable dispersing agents for the silver halide emulsions sensitized according to our invention comprise gelatin, or other colloids, such as collodion, albumen, cellulose organic derivatives, synthetic resins, etc.
What We claim as our invention and desire secured by Letters Patent of the United States is:
1. An unexposed photographic silver halide emulsion containing a sensitizing amount of formamidine sulfinic acid.
2. An unexposed photographic gelatino-silver-halide developing-out emulsion containing a sensitizing amount of formamidine sulfinic acid.
3. An unexposed photographic gelatino-silver bromiodide developing-out emulsion containing a sensitizing amount of formamidine sulfinic acid.
4. An unexposed photographic silver halide emulsion containing a sensitizing amount of formamidine sulfinic acid and a sulfur-sensitizer.
5. An unexposed gold-sensitized photographic silver halide emulsion containing a sensitizing amount of formamidine sulfinic acid.
6. An unexposed acid photographic silver halide emulsion containing a sensitizing amount of formamidine Scase et al Nov. 11, 1941 Weber et a1. Jan. 18, 1944 Weber May 15, 1945
Claims (1)
1. AN UNEXPOSED PHOTOGRAPHIC SILVER HALIDE EMULSION CONTAINING A SENSITIZING AMOUNT OF FORMAMIDINE SULFINIC ACID.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US629459A US2983609A (en) | 1956-12-20 | 1956-12-20 | Chemical sensitization of photographic emulsions |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US629459A US2983609A (en) | 1956-12-20 | 1956-12-20 | Chemical sensitization of photographic emulsions |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US2983609A true US2983609A (en) | 1961-05-09 |
Family
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Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US629459A Expired - Lifetime US2983609A (en) | 1956-12-20 | 1956-12-20 | Chemical sensitization of photographic emulsions |
Country Status (1)
| Country | Link |
|---|---|
| US (1) | US2983609A (en) |
Cited By (16)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3295969A (en) * | 1961-04-12 | 1967-01-03 | Eastman Kodak Co | Photographic spirit duplicating process |
| US3466173A (en) * | 1965-11-30 | 1969-09-09 | Keuffel & Esser Co | Silver halide element containing a developer and aromatic sulfinic acid stabilizers |
| FR2320581A1 (en) * | 1975-08-02 | 1977-03-04 | Konishiroku Photo Ind | PROCESS FOR FORMING A COLOR PHOTOGRAPHIC IMAGE |
| EP0106306A2 (en) | 1982-10-14 | 1984-04-25 | Fuji Photo Film Co., Ltd. | Silver halide color photographic materials |
| EP0115351A2 (en) | 1983-01-28 | 1984-08-08 | Fuji Photo Film Co., Ltd. | Silver halide light-sensitive material |
| EP0147854A2 (en) | 1983-12-29 | 1985-07-10 | Fuji Photo Film Co., Ltd. | Silver halide photographic light-sensitive materials |
| EP0200206A2 (en) | 1985-04-30 | 1986-11-05 | Konica Corporation | Silver halide photographic light-sensitive material |
| EP0201027A2 (en) | 1985-04-30 | 1986-11-12 | Konica Corporation | Silver halide photographic light-sensitive material |
| EP0202784A2 (en) | 1985-04-23 | 1986-11-26 | Konica Corporation | Silver halide photographic light-sensitive material |
| EP0209118A2 (en) | 1985-07-17 | 1987-01-21 | Konica Corporation | Silver halide photographic material |
| EP0228084A2 (en) | 1985-12-25 | 1987-07-08 | Fuji Photo Film Co., Ltd. | Image forming process |
| EP0239363A2 (en) | 1986-03-25 | 1987-09-30 | Konica Corporation | Light-sensitive silver halide photographic material feasible for high speed processing |
| EP0476327A1 (en) | 1990-08-20 | 1992-03-25 | Fuji Photo Film Co., Ltd. | Data-retainable photographic film product and process for producing color print |
| EP0580041A2 (en) | 1992-07-10 | 1994-01-26 | Fuji Photo Film Co., Ltd. | Method of processing silver halide photographic material and composition for processing |
| EP0589460A1 (en) | 1992-09-24 | 1994-03-30 | Fuji Photo Film Co., Ltd. | Method for processing a black & white silver halide light-sensitive material |
| US6040129A (en) * | 1999-04-09 | 2000-03-21 | Eastman Kodak Company | Photographic emulsion having an improved speed, photographic element containing said emulsion, and method |
Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2262055A (en) * | 1940-01-25 | 1941-11-11 | Du Pont Film Mfg Corp | Method of color photography |
| US2339309A (en) * | 1941-09-25 | 1944-01-18 | Du Pont | Photographic reducing composition and process |
| US2376297A (en) * | 1944-01-14 | 1945-05-15 | Du Pont | Process of color photography |
-
1956
- 1956-12-20 US US629459A patent/US2983609A/en not_active Expired - Lifetime
Patent Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2262055A (en) * | 1940-01-25 | 1941-11-11 | Du Pont Film Mfg Corp | Method of color photography |
| US2339309A (en) * | 1941-09-25 | 1944-01-18 | Du Pont | Photographic reducing composition and process |
| US2376297A (en) * | 1944-01-14 | 1945-05-15 | Du Pont | Process of color photography |
Cited By (16)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3295969A (en) * | 1961-04-12 | 1967-01-03 | Eastman Kodak Co | Photographic spirit duplicating process |
| US3466173A (en) * | 1965-11-30 | 1969-09-09 | Keuffel & Esser Co | Silver halide element containing a developer and aromatic sulfinic acid stabilizers |
| FR2320581A1 (en) * | 1975-08-02 | 1977-03-04 | Konishiroku Photo Ind | PROCESS FOR FORMING A COLOR PHOTOGRAPHIC IMAGE |
| EP0106306A2 (en) | 1982-10-14 | 1984-04-25 | Fuji Photo Film Co., Ltd. | Silver halide color photographic materials |
| EP0115351A2 (en) | 1983-01-28 | 1984-08-08 | Fuji Photo Film Co., Ltd. | Silver halide light-sensitive material |
| EP0147854A2 (en) | 1983-12-29 | 1985-07-10 | Fuji Photo Film Co., Ltd. | Silver halide photographic light-sensitive materials |
| EP0202784A2 (en) | 1985-04-23 | 1986-11-26 | Konica Corporation | Silver halide photographic light-sensitive material |
| EP0201027A2 (en) | 1985-04-30 | 1986-11-12 | Konica Corporation | Silver halide photographic light-sensitive material |
| EP0200206A2 (en) | 1985-04-30 | 1986-11-05 | Konica Corporation | Silver halide photographic light-sensitive material |
| EP0209118A2 (en) | 1985-07-17 | 1987-01-21 | Konica Corporation | Silver halide photographic material |
| EP0228084A2 (en) | 1985-12-25 | 1987-07-08 | Fuji Photo Film Co., Ltd. | Image forming process |
| EP0239363A2 (en) | 1986-03-25 | 1987-09-30 | Konica Corporation | Light-sensitive silver halide photographic material feasible for high speed processing |
| EP0476327A1 (en) | 1990-08-20 | 1992-03-25 | Fuji Photo Film Co., Ltd. | Data-retainable photographic film product and process for producing color print |
| EP0580041A2 (en) | 1992-07-10 | 1994-01-26 | Fuji Photo Film Co., Ltd. | Method of processing silver halide photographic material and composition for processing |
| EP0589460A1 (en) | 1992-09-24 | 1994-03-30 | Fuji Photo Film Co., Ltd. | Method for processing a black & white silver halide light-sensitive material |
| US6040129A (en) * | 1999-04-09 | 2000-03-21 | Eastman Kodak Company | Photographic emulsion having an improved speed, photographic element containing said emulsion, and method |
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