US3520689A - Color developing process utilizing pyridinium salts - Google Patents
Color developing process utilizing pyridinium salts Download PDFInfo
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- US3520689A US3520689A US557610A US3520689DA US3520689A US 3520689 A US3520689 A US 3520689A US 557610 A US557610 A US 557610A US 3520689D A US3520689D A US 3520689DA US 3520689 A US3520689 A US 3520689A
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- color
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- silver
- developing
- aminophenol
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- 238000000034 method Methods 0.000 title description 13
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical class C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 title description 7
- PLIKAWJENQZMHA-UHFFFAOYSA-N 4-aminophenol Chemical compound NC1=CC=C(O)C=C1 PLIKAWJENQZMHA-UHFFFAOYSA-N 0.000 description 23
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 23
- 238000004061 bleaching Methods 0.000 description 17
- 229910052709 silver Inorganic materials 0.000 description 16
- 239000004332 silver Substances 0.000 description 16
- BQCADISMDOOEFD-UHFFFAOYSA-N Silver Chemical compound [Ag] BQCADISMDOOEFD-UHFFFAOYSA-N 0.000 description 15
- 238000011109 contamination Methods 0.000 description 15
- 150000001875 compounds Chemical class 0.000 description 13
- 238000012545 processing Methods 0.000 description 13
- 229910052708 sodium Inorganic materials 0.000 description 12
- 239000011734 sodium Substances 0.000 description 12
- 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 11
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 11
- 229910052700 potassium Inorganic materials 0.000 description 11
- 239000011591 potassium Substances 0.000 description 11
- 150000001767 cationic compounds Chemical class 0.000 description 9
- 230000000694 effects Effects 0.000 description 8
- 239000000203 mixture Substances 0.000 description 8
- ZFIQGRISGKSVAG-UHFFFAOYSA-N 4-methylaminophenol Chemical compound CNC1=CC=C(O)C=C1 ZFIQGRISGKSVAG-UHFFFAOYSA-N 0.000 description 6
- 125000000217 alkyl group Chemical group 0.000 description 5
- 239000000839 emulsion Substances 0.000 description 5
- ZUNKMNLKJXRCDM-UHFFFAOYSA-N silver bromoiodide Chemical compound [Ag].IBr ZUNKMNLKJXRCDM-UHFFFAOYSA-N 0.000 description 5
- CBCKQZAAMUWICA-UHFFFAOYSA-N 1,4-phenylenediamine Chemical compound NC1=CC=C(N)C=C1 CBCKQZAAMUWICA-UHFFFAOYSA-N 0.000 description 4
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 4
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 4
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
- 229920002301 cellulose acetate Polymers 0.000 description 3
- 239000003795 chemical substances by application Substances 0.000 description 3
- NLKNQRATVPKPDG-UHFFFAOYSA-M potassium iodide Chemical compound [K+].[I-] NLKNQRATVPKPDG-UHFFFAOYSA-M 0.000 description 3
- -1 silver halide Chemical class 0.000 description 3
- AEEZXQFUVDKVFT-UHFFFAOYSA-N 2-(benzylamino)phenol Chemical compound OC1=CC=CC=C1NCC1=CC=CC=C1 AEEZXQFUVDKVFT-UHFFFAOYSA-N 0.000 description 2
- SRYYOKKLTBRLHT-UHFFFAOYSA-N 4-(benzylamino)phenol Chemical compound C1=CC(O)=CC=C1NCC1=CC=CC=C1 SRYYOKKLTBRLHT-UHFFFAOYSA-N 0.000 description 2
- 229940126062 Compound A Drugs 0.000 description 2
- NLDMNSXOCDLTTB-UHFFFAOYSA-N Heterophylliin A Natural products O1C2COC(=O)C3=CC(O)=C(O)C(O)=C3C3=C(O)C(O)=C(O)C=C3C(=O)OC2C(OC(=O)C=2C=C(O)C(O)=C(O)C=2)C(O)C1OC(=O)C1=CC(O)=C(O)C(O)=C1 NLDMNSXOCDLTTB-UHFFFAOYSA-N 0.000 description 2
- 125000004432 carbon atom Chemical group C* 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- 125000000325 methylidene group Chemical group [H]C([H])=* 0.000 description 2
- 230000035945 sensitivity Effects 0.000 description 2
- 229910000029 sodium carbonate Inorganic materials 0.000 description 2
- VPMMJSPGZSFEAH-UHFFFAOYSA-N 2,4-diaminophenol;hydrochloride Chemical compound [Cl-].NC1=CC=C(O)C([NH3+])=C1 VPMMJSPGZSFEAH-UHFFFAOYSA-N 0.000 description 1
- CDAWCLOXVUBKRW-UHFFFAOYSA-N 2-aminophenol Chemical class NC1=CC=CC=C1O CDAWCLOXVUBKRW-UHFFFAOYSA-N 0.000 description 1
- XBTWVJKPQPQTDW-UHFFFAOYSA-N 4-n,4-n-diethyl-2-methylbenzene-1,4-diamine Chemical compound CCN(CC)C1=CC=C(N)C(C)=C1 XBTWVJKPQPQTDW-UHFFFAOYSA-N 0.000 description 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 1
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 1
- 235000014443 Pyrus communis Nutrition 0.000 description 1
- VXVXRJJWYPVNLM-UHFFFAOYSA-N [2-(methylamino)phenyl] hydrogen sulfate Chemical compound CNC1=CC=CC=C1OS(O)(=O)=O VXVXRJJWYPVNLM-UHFFFAOYSA-N 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 125000006367 bivalent amino carbonyl group Chemical group [H]N([*:1])C([*:2])=O 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 230000007812 deficiency Effects 0.000 description 1
- 230000003993 interaction Effects 0.000 description 1
- 150000004682 monohydrates Chemical class 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- JUJWROOIHBZHMG-UHFFFAOYSA-O pyridinium Chemical compound C1=CC=[NH+]C=C1 JUJWROOIHBZHMG-UHFFFAOYSA-O 0.000 description 1
- WFKWXMTUELFFGS-UHFFFAOYSA-N tungsten Chemical compound [W] WFKWXMTUELFFGS-UHFFFAOYSA-N 0.000 description 1
- 229910052721 tungsten Inorganic materials 0.000 description 1
- 239000010937 tungsten Substances 0.000 description 1
- 125000004417 unsaturated alkyl group Chemical group 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D213/00—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
- C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
- C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D213/06—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom containing only hydrogen and carbon atoms in addition to the ring nitrogen atom
- C07D213/16—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom containing only hydrogen and carbon atoms in addition to the ring nitrogen atom containing only one pyridine ring
- C07D213/20—Quaternary compounds thereof
-
- 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
- G03C7/00—Multicolour photographic processes or agents therefor; Regeneration of such processing agents; Photosensitive materials for multicolour processes
- G03C7/30—Colour processes using colour-coupling substances; Materials therefor; Preparing or processing such materials
- G03C7/407—Development processes or agents therefor
- G03C7/413—Developers
Definitions
- An improved color developer is prepared by combining a p-phenylene diamine with (A) a cationic compound selected from the group consisting of a cationic compound having a pyridinium group represented by the general formula and a cationic compound having the pyridinium group represented by the general formula:
- A represents an atomic group consisting of a methylene chain and a group selected from O, --NHCO-, and OCO
- B represents a member selected from a saturated alkyl group, an unsaturated alkyl group and a hydrogen atom
- R and R represent a member selected from a hydrogen atom and an alkyl group having 1 to 5 carbon atoms
- X- represents a member selected from 2C1, 2Br-, SO and 2ClO
- Y- represents a member selected from Cl", Br, and C 1 and (B) at least one member selected from a group consisting of N-methyl-p-aminophenol, o,p-diamino phenol, N-benzyl-p-aminophenol and p-aminophenol.
- the present invention relates generally to a color developing process for a silver halide color photographic element and more particularly to a color developing process using a cationic compound of a pyridinium salt type and p-aminophenol or its derivatives thereof to promote the color developing, reducing the deficiency in silver bleaching and color contamination while improving picture quality.
- the presence of the developing accelerator in a bleaching process for developed silver after the color development frequently reduce the oxidation speed of silver, that is, causes the phenomenon of co-called insuflicient silver bleaching.
- an object of the present invention is to accelerate the color developing speed and increase the color density.
- Another object of the present invention is to improve the silver-bleaching in color photographic processing.
- Still a further object of the present invention is to reduce or prevent the contamination or color contamination in color photography.
- pyridinium-type cationic compounds to be used in the present invention may be represented by the following general formulas:
- the p-aminophenol derivatives used in the present invention are N-methylaminophenol sulfate metol), o,pdiaminophenol hydrochloride (amidol), and N-benzyl-paminophenol. Although the effect may be slightly less than those of the above-mentioned aminophenol derivatives, p-arninophenol may be also used in this invention. In this respect, it must be understood that the use of p-aminophenol or its derivatives among black and white developing agents is important in this invention since the use of other black and white developing agents together with the abovementioned developing accelerators increases, on the contrary, the contamination or color contamination.
- a suitable amount of p-aminophenol or its derivatives thereof to be added in the developer is 0.1 to 1 g./l.
- the amount may be less or higher than the range but if the amount is less than 0.1 g./l. the effect of the addition thereof becomes insufficient and if higher than 1 -g./l. the color density tends to be reduced on the contrary.
- Two or more kinds of the above-mentioned p-aminophenol and its derivatives thereof may be used in this invention.
- the present invention may be generally applied to color photographic materials using a color developer containing p-phenylenediamine or its derivatives thereof, such as color negative films, photographic color papers, photographic color reversal films and the like.
- a color developer containing p-phenylenediamine or its derivatives thereof such as color negative films, photographic color papers, photographic color reversal films and the like.
- the most effective results of this invention can be obtained in the case of conducting this invention about a yellow color developer for photographic color reversal film having technical difiiculties in silver bleaching and color contamination.
- EXAMPLE 1 A test sample which had been prepared by applying a blue-sensitive gelatino silver bromo-iodide emulsion to a cellulose acetate film was exposed by means of a sensitometer and subjected to the following processings:
- compositions of the processing baths were as follows:
- the color density and the silver-bleaching elfect were measured in this processing as about the same as when using the pyridinium compounds, the p-aminophenol derivatives or both, the results of which are shown in Table 1.
- the color density is shown by the value by measuring the maximum density range of thus processed film using a blue filter light and the silver bleaching effect is shown by the value of the blackened density (D by the remaining silver measured by using a red filter light divided by the color density value (D obtained from measuring by using a blue filter light.
- EXAMPLE 2 To a cellulose acetate film were applied a red-sensitive gelatino silver bromo-iodide emulsion, a green-sensitive gelatino silverbromo-iodide emulsion, a yellow filter layer composed of colloidal silver for absorbing blue light, and a blue-sensitive silver bromo-iodide emulsion in the order to provide a multilayer color photographic film, which was exposed using a sensitometer and subjected to the following processings:
- compositions of the first developer and the second black and white developer were the same as the composition of the first developer in Example 1.
- Other compositions of the processing solutions were as follows:
- the composition of the yellow developer was same as that of the color developer in Example 1.
- compositions of the bleaching solution and the fixing solution were the same as those in Example 1.
- the effect of the addition of the compounds of this invention to the yellow color developer in the above processings is shown in Table 2.
- the color density (D ) was measured by a blue filter light.
- the silver bleaching was measured about samples exposed to yellow patch.
- the color contamination (1) shows the ratio of the color density (D obtained by measuring with green filter light a sample exposed to yellow patch to the color density (D obtained by measuring it with blue filter light, that is, the ratio of unnecessary magenta color components in the yellow image
- the color contamination (2) shows the ratio of the color density (D obtained by measuring with blue filter light a sample exposed to magenta patch to the color density (D- obtained by measuring it with green filter light, that is, the ratio of unnecessary yellow components in the magenta image.
- EXAMPLE 4 A gelatino silver bromo-iodide emulsion containing a yellow coupler was applied to a cellulose acetate film to provide a test sample, which was exposed by means of a NSG sensitorneter and then subjected to the following processings:
- compositions of the processing solutions were as follows:
- Fixing solution (first) Sodium sulfiteg. Sodium thiosulfate-ISO g. Acetic acid (28% )-48 ml. Boric acid-7 g. Potassium alum15 g. Water to make 1 liter.
- a color developing process for color photographic silver halide materials using a color developer containing a member selected from the group consisting of p-phenylenediamine and the derivatives thereof the improvement which comprises using said color developer having added therein -(A) a member selected from the group consisting of a'cationic compound having the pyridinium group represented by the general formula and a cationic compound having the pyridinium group represented by the general formula wherein A represents an atomic group consisting of a methylene chain and a group selected from O--, NHCO-, and- OCO-; B represents a member selected from a saturated alkyl group, an unsaturted alkyl group and a hydrogen atom; R and R represent a member selected from a hydrogen atom and an alkyl group having 1 to 5 carbon atoms; X- represents a member selected from 2Cl*, 2Br, 80.;- and 200;; and Y- represents a member selected from Ch, Br" and 010 and (
Description
United States Patent .0
US. Cl. 96-55 Claims ABSTRACT OF THE DISCLOSURE An improved color developer is prepared by combining a p-phenylene diamine with (A) a cationic compound selected from the group consisting of a cationic compound having a pyridinium group represented by the general formula and a cationic compound having the pyridinium group represented by the general formula:
wherein A represents an atomic group consisting of a methylene chain and a group selected from O, --NHCO-, and OCO; B represents a member selected from a saturated alkyl group, an unsaturated alkyl group and a hydrogen atom; R and R represent a member selected from a hydrogen atom and an alkyl group having 1 to 5 carbon atoms; X- represents a member selected from 2C1, 2Br-, SO and 2ClO Y- represents a member selected from Cl", Br, and C 1 and (B) at least one member selected from a group consisting of N-methyl-p-aminophenol, o,p-diamino phenol, N-benzyl-p-aminophenol and p-aminophenol. Use of these compounds in the color developing process results in a film having reduced color contamination, increased color density, and improved silver bleaching.
The present invention relates generally to a color developing process for a silver halide color photographic element and more particularly to a color developing process using a cationic compound of a pyridinium salt type and p-aminophenol or its derivatives thereof to promote the color developing, reducing the deficiency in silver bleaching and color contamination while improving picture quality.
Since a conventional color developer containing as a color developing agent p-phenylencdiamine or its derivatives is low in developing po'wer compared with that of a general black and white developer, the pH value of the processing solution has been raised or the developing procedure has been conducted for a very long period of time. Accordingly, there have hitherto been employed color developing accelerators, but the use of such conventional color developing accelerators frequently causes fogging at unexposed areas resulting in contaminating the picture or images. Further, if the developing time is shortened for preventing the formation of fog, no increase in the color density of the image portions is observed and hence the color developing processing cannot be conducted effectively.
In particular, in a color developing process using a 3,520,689 Patented July 14, 1970 color developer containing couplers therein, the use of accelerators frequently causes undesirable color fogging or color contamination.
Further, the presence of the developing accelerator in a bleaching process for developed silver after the color development frequently reduce the oxidation speed of silver, that is, causes the phenomenon of co-called insuflicient silver bleaching.
Thus, there are presently very few color development accelerators having excellent properties in the above mentioned points.
Accordingly, an object of the present invention is to accelerate the color developing speed and increase the color density.
Another object of the present invention is to improve the silver-bleaching in color photographic processing.
Still a further object of the present invention is to reduce or prevent the contamination or color contamination in color photography.
It has been found that by using a color developer containing p-phenylenediamine or its derivatives added with a pyridinium type cationic compound and p-aminophenol or its derivatives, the color developing speed can be remarkably increased as Well as the silver bleaching improved and hence contamination or color contamination can be reduced to improve the quality of photographic pictures.
It has been known that the use of pyridinium-type cationic compounds alone accelerate developing speed, but it gives at the same time undesirable results in contamination or color contamination. Further, if some kinds of couplers are present at color development, the use of such a developing accelerator will cause insufficient silver bleaching. However, if the developing accelerator is used together with p-aminophenol or its derivatives thereof in color development, the developing speed is accelerated more effectively as compared with the case of using the developing accelerator alone as well as the abovementioned various faults are reduced.
The pyridinium-type cationic compounds to be used in the present invention may be represented by the following general formulas:
M- kx L X- and pear and if it is too small, the effect of the addition there of will be weak. Therefore, the amount of 0.03 g./l. to
0.5 g./l. is preferable.
The p-aminophenol derivatives used in the present invention are N-methylaminophenol sulfate metol), o,pdiaminophenol hydrochloride (amidol), and N-benzyl-paminophenol. Although the effect may be slightly less than those of the above-mentioned aminophenol derivatives, p-arninophenol may be also used in this invention. In this respect, it must be understood that the use of p-aminophenol or its derivatives among black and white developing agents is important in this invention since the use of other black and white developing agents together with the abovementioned developing accelerators increases, on the contrary, the contamination or color contamination. Further, if the above-mentioned p-aminophenol or its derivatives are added alone in a color developer, a black and white development occurs together with a color development, which results in the reduction of color density and only if the amount thereof is properly selected some extent of the increase in color density is observed in a limited range of exposure and developing time. However, if the abovementioned pyridinium salt compounds are present together with the p-aminophenol derivative or p-aminophenol in a color developer, the color density can be remarkably increased without increasing color fog.
A suitable amount of p-aminophenol or its derivatives thereof to be added in the developer is 0.1 to 1 g./l. The amount may be less or higher than the range but if the amount is less than 0.1 g./l. the effect of the addition thereof becomes insufficient and if higher than 1 -g./l. the color density tends to be reduced on the contrary. Two or more kinds of the above-mentioned p-aminophenol and its derivatives thereof may be used in this invention.
Thus, by using the above-mentioned two compounds according to the present invention, said two compounds being impracticable individually owing to their drawbacks, the faults of the two compounds are compensated by each other to make possible the practical use thereof as well as an unexpected remarkable development accelerating effect from the interaction of them.
The present invention may be generally applied to color photographic materials using a color developer containing p-phenylenediamine or its derivatives thereof, such as color negative films, photographic color papers, photographic color reversal films and the like. In particular, the most effective results of this invention can be obtained in the case of conducting this invention about a yellow color developer for photographic color reversal film having technical difiiculties in silver bleaching and color contamination.
The following examples illustrate but do not limit the present invention:
EXAMPLE 1 A test sample which had been prepared by applying a blue-sensitive gelatino silver bromo-iodide emulsion to a cellulose acetate film was exposed by means of a sensitometer and subjected to the following processings:
First development-3 min. at 27 C.
Water rinsing4 min.
Reversal exposure (tungsten lamp)-20O CMS Color development-5 min.
Water rinsing-- 4 min.
Bleaching-2 min.
Water rinsing1 min.
Fixing-2 min.
Water rinsing2 min.
The compositions of the processing baths were as follows:
First developer:
N-Methyl-p-aminophenol sulfate-2.0 g. Sodium sulfite90.0 g. Hydroquinone8.0 g.
Sodium carbonate (monohydrate)52.5 g. Potassium bromide-5 .0 g.
Potassium thiocyanate1.0 g.
Water to make 1 liter.
Color developer:
Sodium sulfite--5.* g. p-Amino-N,N-diethylaniline sulfite2.5 g. Potassium bromide1.0 g. Potassium iodide (0.1% aq. soln.) ml. 1-w-benzoyl-4- p-toluene sulfonamido) acetanilide-1.2 g.
Sodium hydroxideg. Water to make 1 liter.
Bleaching solution Potassium ferricyanide100 g. Potassium bromide-10 g. Borax-2 g. Boric acid-l g. Water to make 1 liter.
Fixing solution Sodium thiosulfate--l50 g. Sodium sulfitel0 g. Water to make 1 liter.
The color density and the silver-bleaching elfect were measured in this processing as about the same as when using the pyridinium compounds, the p-aminophenol derivatives or both, the results of which are shown in Table 1. The color density is shown by the value by measuring the maximum density range of thus processed film using a blue filter light and the silver bleaching effect is shown by the value of the blackened density (D by the remaining silver measured by using a red filter light divided by the color density value (D obtained from measuring by using a blue filter light.
TABLE 1 Compound added in color developer Compound A Benzylamino- Color density Silver bleaching (g./l.) phenol (g./l.) D B max. efiect D /D From the table, it is clear that a yellow color image having high color density and high transparency was obtained by using Compound (A) and benzylaminophenol together as comparedwith the cases of using Compound (A) or benzylaminophenol individually.
EXAMPLE 2 To a cellulose acetate film were applied a red-sensitive gelatino silver bromo-iodide emulsion, a green-sensitive gelatino silverbromo-iodide emulsion, a yellow filter layer composed of colloidal silver for absorbing blue light, and a blue-sensitive silver bromo-iodide emulsion in the order to provide a multilayer color photographic film, which was exposed using a sensitometer and subjected to the following processings:
First development-4 min., at 27 C. Water rinsing--4 min.
Reversal red exposure-100 CMS Cyan color development-5 min. Water rinsing 2 min.
Reversal blue exposure-200 CMS Yellow color development-5 min. Second black and white development--2 min. Water rinsing-2 min.
Reversal white exposure-2000 CMS Magenta color development-5 min. Water rinsing-4 min.
Bleaching-2 min.
Water rinsing-1 min.
Fixing-2 min. Water rinsing-2 min.
The compositions of the first developer and the second black and white developer were the same as the composition of the first developer in Example 1. Other compositions of the processing solutions were as follows:
Cyan color developer:
Sodium sulfite5.0 g. 4-arnino-3-methyl-N.N-diethylaniline hydrochloridel.5 g.
Sodium carbonate (mono-hydrate)-15.0 g. Potassium bromide1.0 g. Potassium iodide (0.1% aq. soln.)-2 ml. 1,S-dihydroxy-Z,6-dibromonaphthalenel.2 g. Sodium hydroxide-2.0 g. Water to make 1 liter.
The composition of the yellow developer was same as that of the color developer in Example 1.
Magenta color developer:
4-amino-3-methyl-N,N-diethylaniline hydrochloride-2.0 g.
Potassium bromide-0.2 g.
1-phenyl-3-(m-nitrobenzoylamino) -5-pyraz0lone-- Sodium hydroxide2.5 g.
n-Butylamine5 ml.
Water to make 1 liter.
The compositions of the bleaching solution and the fixing solution were the same as those in Example 1.
The effect of the addition of the compounds of this invention to the yellow color developer in the above processings is shown in Table 2. In the table, the color density (D )was measured by a blue filter light. The silver bleaching was measured about samples exposed to yellow patch. The color contamination (1) shows the ratio of the color density (D obtained by measuring with green filter light a sample exposed to yellow patch to the color density (D obtained by measuring it with blue filter light, that is, the ratio of unnecessary magenta color components in the yellow image and the color contamination (2) shows the ratio of the color density (D obtained by measuring with blue filter light a sample exposed to magenta patch to the color density (D- obtained by measuring it with green filter light, that is, the ratio of unnecessary yellow components in the magenta image.
TABLE 2 Silver Color con Color eon- Addltion compounds Color bleaching tarninatarninaensity effect tion (1) tion (2) Compound A Metol (D (DB/D a) R/D a) B/ o) O 3. 0 0. l3 0. 83 0. 35 0 3. 2 0. 15 0. 60 0. 36 0. 2 3. 15 0. 08 0. 44 0. 32 0. l5 3. 25 0. 10 0. 52 0. 32 0. 2 3. 65 0. 08 0. 42 0. 32 0. 3 3. 5 0. 06 0. 37 0. 32
EXAMPLE 3 By repeating the procedure in Example 2 using a standard composition as the yellow color developer while added the compounds of this invention in the cyan color developer, the results shown in Table 3 were obtained.
7 necessary yellow components in the cyan color patch and the color contamination (2) shows unnecessary cyan color components inthe yellow patch.
EXAMPLE 4 A gelatino silver bromo-iodide emulsion containing a yellow coupler was applied to a cellulose acetate film to provide a test sample, which was exposed by means of a NSG sensitorneter and then subjected to the following processings:
Color development-S min, at 24 C. Water rinsing-30 sec.
First fixing-4 min.
Water rinsing-5 min.
Bleaching-4 min.
Water rinsing-5 min.
Second fixing4 min.
Water rinsing5 min.
The compositions of the processing solutions were as follows:
Fixing solution: (first) Sodium sulfiteg. Sodium thiosulfate-ISO g. Acetic acid (28% )-48 ml. Boric acid-7 g. Potassium alum15 g. Water to make 1 liter.
Bleaching solution:
Potassium bromideg. Potassium dichromate5 g. Potassium alum-40 g. Sodium acetate--8 g. Acetic acid57 ml. Water to make 1 liter.
Fixing solution (second):
Sodium thiosulfate150 g. Sodium sulfite--15 g. Potassium alum-15 g. Water to make 1 liter.
The results of adding the compounds of this invention in the color developer in the above processings are shown in Table 4.
TABLE 4 Silver Addition Compound Color bleaching density Relative effect Compound B Metol (D sensitivity (D /D Color fog In the table, the relative sensitivity was shown by the relative value of the logarithmic exposure amount at the point where the density reaches fog +0.2.
We claim:
1. In a color developing process for color photographic silver halide materials using a color developer containing a member selected from the group consisting of p-phenylenediamine and the derivatives thereof, the improvement which comprises using said color developer having added therein -(A) a member selected from the group consisting of a'cationic compound having the pyridinium group represented by the general formula and a cationic compound having the pyridinium group represented by the general formula wherein A represents an atomic group consisting of a methylene chain and a group selected from O--, NHCO-, and- OCO-; B represents a member selected from a saturated alkyl group, an unsaturted alkyl group and a hydrogen atom; R and R represent a member selected from a hydrogen atom and an alkyl group having 1 to 5 carbon atoms; X- represents a member selected from 2Cl*, 2Br, 80.;- and 200;; and Y- represents a member selected from Ch, Br" and 010 and (B) at least one member selected from N-methyl-p-aminophenol, o,p-diaminophenol, N-benzyl p aminophenol and paminophenol, o,p.-diaminophenol,. N-lbenxyl-p-aminophee nol and p-aminophenol.
2. The color developing process as in claim 1, wherein the amount of said component (B) to the color developer is 0.1-1 g./liter.
3. The color developing process as in claim 1, wherein the amount of said component (A) to the color developer is 0.03( ).5 g./liter.
4. The color developing process as in claim 1, wherein said color developer containing said component (A) and said component (B) is a color developer with or without couplers for processing color photographic elements.
5. The color developing process as in claim 4, wherein said color photographic element is a photographic reversal color film to be processed in a coupler containing developer.
I References Cited UNITED STATES PATENTS 2,648,604 8/1953 Welliver etal. ,96-66.3' 3,062,645 11/1962 Carroll 96-55 3,300,305 1/196-7 Pesch et al. -9622 J. TRAVIS BROWN, Primary Examiner US. Cl. XJR.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP3583565 | 1965-06-16 |
Publications (1)
Publication Number | Publication Date |
---|---|
US3520689A true US3520689A (en) | 1970-07-14 |
Family
ID=12453011
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US557610A Expired - Lifetime US3520689A (en) | 1965-06-16 | 1966-06-15 | Color developing process utilizing pyridinium salts |
Country Status (4)
Country | Link |
---|---|
US (1) | US3520689A (en) |
BE (1) | BE682559A (en) |
DE (1) | DE1547844A1 (en) |
GB (1) | GB1112538A (en) |
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US3813244A (en) * | 1972-07-24 | 1974-05-28 | Eastman Kodak Co | 'onium indo-n-arylsulfoaniline |
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US2648604A (en) * | 1951-12-28 | 1953-08-11 | Gen Aniline & Film Corp | Photographic developer containing a pyridinium salt and process of development |
US3062645A (en) * | 1957-11-27 | 1962-11-06 | Eastman Kodak Co | Sensitization of photographic emulsions to be developed with p-phenylenediamine developing agents |
US3300305A (en) * | 1962-10-25 | 1967-01-24 | Eastman Kodak Co | Color developers containing competing developing agents |
-
1966
- 1966-06-15 US US557610A patent/US3520689A/en not_active Expired - Lifetime
- 1966-06-15 BE BE682559D patent/BE682559A/xx unknown
- 1966-06-15 GB GB26733/66A patent/GB1112538A/en not_active Expired
- 1966-06-16 DE DE19661547844 patent/DE1547844A1/en active Pending
Patent Citations (3)
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US2648604A (en) * | 1951-12-28 | 1953-08-11 | Gen Aniline & Film Corp | Photographic developer containing a pyridinium salt and process of development |
US3062645A (en) * | 1957-11-27 | 1962-11-06 | Eastman Kodak Co | Sensitization of photographic emulsions to be developed with p-phenylenediamine developing agents |
US3300305A (en) * | 1962-10-25 | 1967-01-24 | Eastman Kodak Co | Color developers containing competing developing agents |
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Also Published As
Publication number | Publication date |
---|---|
BE682559A (en) | 1966-11-14 |
DE1547844A1 (en) | 1970-02-19 |
GB1112538A (en) | 1968-05-08 |
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