US3003877A - Spot prevention in photographic emulsions and colloid layers - Google Patents

Spot prevention in photographic emulsions and colloid layers Download PDF

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US3003877A
US3003877A US668316A US66831657A US3003877A US 3003877 A US3003877 A US 3003877A US 668316 A US668316 A US 668316A US 66831657 A US66831657 A US 66831657A US 3003877 A US3003877 A US 3003877A
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synthetic
gelatin
tannic acid
acid
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Leonard T Mclaughlin
Bill R Burks
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Eastman Kodak Co
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    • GPHYSICS
    • G03PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
    • G03CPHOTOSENSITIVE MATERIALS FOR PHOTOGRAPHIC PURPOSES; PHOTOGRAPHIC PROCESSES, e.g. CINE, X-RAY, COLOUR, STEREO-PHOTOGRAPHIC PROCESSES; AUXILIARY PROCESSES IN PHOTOGRAPHY
    • G03C1/00Photosensitive materials
    • G03C1/005Silver halide emulsions; Preparation thereof; Physical treatment thereof; Incorporation of additives therein
    • G03C1/06Silver halide emulsions; Preparation thereof; Physical treatment thereof; Incorporation of additives therein with non-macromolecular additives
    • G03C1/38Dispersants; Agents facilitating spreading
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10STECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10S430/00Radiation imagery chemistry: process, composition, or product thereof
    • Y10S430/152Making camera copy, e.g. mechanical negative

Definitions

  • This invention relates to improved photographic coatings comprising a synthetic spreading agent and tannic acid.
  • saponin can be used in gelatin coating compositions for the purpose of obtaining uniform coatings substantially free of bare spots and other surface imperfections. It is also known that commercial saponin varies considerably from batch to batch, such variations making it quite difficult at times to obtain uniform results in the coatings.
  • Certain photographic coating solutions contain minute metallic iron or iron compounds as impurities and when photographic coatings containing such impurities and the synthetic coating aids are processed in the normal manner, small desensitized areas, or areas of reduced density appear in the course of the process. These small areas of reduced density show up as white spots, thus producing a rather serious defect in the final photographic print.
  • tannic acid can be added directlyv to ordinary gelatino-silver-halide emulsions containing synthetic spreading agents as coating aids, or to other photographic gelatin coating vsolutions containing no light-sensitive material, such as the coatings generally employed in imbibition printing blanks.
  • tannic acid can be added to gelatin Alternatively, the
  • the synthetic coating aids used as a replacement for commercial saponin are generally compounds containing a hydrophobic moiety, such as a long-chain alkyl group, in combination with a hydrophilic moiety, such as sulfonic acid salt groups or carboxylic acid salt groups. These synthetic coating aids frequently have an amide group somewhere in the chain. These synthetic coating aids can be classified generically as water-soluble salts of sulfonic or carboxylic acids containing an amido group. While representative synthetic coating aids or spreading agents are illustrated below, it is to be understood that other synthetic agents can be employed to equal advantage in accomplishing the beneficial results afiorded by the tannic acid of our invention. Typical coating aids include those represented by the following general formulas:
  • R-C-N-CHaGHaSOaM E nt-xl-ii-N-omoHio-o-NHdn oHi)d-ioo0M oHioHi0-oNHoH(OHi)d-i 3ooM' l
  • R represents an aliphatic hydrocarbon radical containing at least 8 carbon atoms (e.g., n-octyl, n-decyl, n-myristyl, n-cetyl, oleyl, linoleyl, etc.)
  • R represents an aliphatic radical containing not more than about 4 carbon atoms (e.g., methyl, ethyl, n-propyl, n-butyl, etc.), a cycloalkyl group (e.g., cyclopentyl, cyclohexyl, etc.), or an aryl group (e.g., phenyl, tolyl,
  • R represents the carbocyclic nucleus of a rosin acid, such as'rosinyl, hyro- ,rosinyl, dihydrorosinyl, etc., radicals
  • R represents a lower alkyl group (e.g.,
  • At least 8 carbon atoms such as those radicals listed above with respect to R
  • an' alkaryl group the alkyl portion of which contains at least-8 carbon atoms (e.g.,
  • M represents an alkali metal atom '(e.g., sodium, potassium, etc.), ammonium or organic ammonium (i.e., derivatives where a salt has been formed between the sulfonic acid and an organic amine, such as pyridine, triethylamine, triethanolamine, etc.),
  • n represents a positive integer from 1 to 12
  • x represents a posisi ese o from 1 o .4, m rep en a pc ti e in of from 1 to 2
  • d represents a positive integer of from to 3
  • the synthetic spreading agents represented by Formula 1 above can be prepared as described in US. Patent 2,739,891.
  • the useful synthetic spreading agents 'sclosed in the patent are the alkali metal salts of oleoyl methyl taurine.
  • the synthetic spreading agents represented by Formula II above can be prepared according to the method described in application Serial No. 556,044 mentioned above, as well as US. application Serial No. 600,679.
  • Useful synthetic spreading agents shown in these applications include N-(carbo-p-tertiary octyl phenoxy pentath x glutamate i d m salt, N- ar c-fiamid ethoxy aspartic acid sodium salt, etc.
  • the synthetic spreading agents represented by Formula III above can be prepared as described in Serial No. 603,195 mentioned above.
  • Typical of such synthetic spreading agents are sodium N-carbo-abityl oxy glutamate, N-carbo-abityl-oxy polyethoxy glycine sodium salt, etc.
  • the synthetic spreading agents represented by Forinulas IV an'd V above can be prepared as described in Serial No. 600,679 mentioned above.
  • Typical spreading agents include 3,8,l3-triaza-4,l2-dioxo-5,1l-dioxa-S-lauroyl pentadecane-1,l5-dioic acid sodium salt, etc.
  • oleoyl methyl taurine can be used in an amount varying from about .0055 to .5%, based on the amount of dry gelatin in the coating composition.
  • the most useful amount for a given spreading agent can be determined by running a series of test coatings, wherein the amounts of spreading agent are varied. The point at which the uniform spreading occurs without the formation of dry areas in the coating can be readily observed.
  • the amount of tannic acid used in our invention can be varied, depending upon the source of the gelatin, particular spreading agent being used, and the like. In general, we have found that from about .065 gram to .65 gram per 100 Square feet of coated area is sufiicient for the purposes of our invention.
  • gelatino-silver-halide emulsions When used in gelatino-silver-halide emulsions, it has been noted that particularly useful results have been obtained with the so-called paper emulsions containing silver chlorobromide.
  • gelatino-silverhalide emulsions such as silver chloride, silver bromiodide, silver chlorobromicdide, etc. emulsions can also. be treated according to our invention.
  • Example An ordinary gelatino-silver-chlorobromide emulsion was divided into several batches, and these batches treated with the amounts of tannic acid shown in the following table. Certain of the batches contained sufficient spreading agent to insure uniform coating, these spreading agents being identified in the table.
  • the various emulsions were then coated on an ordinary photographic paper support and the coatings dried and processed in the usual manner. The number of white spots per 8" by 10" sheet were measured for the fresh coatings, as well as for the coatings after incubation for eight days at 120 F. and three months under storage under ambient conditions. The number of white spots for each of the three conditions 1s given in the following table.
  • Example 2 The same emulsion batch used in Example 1 above was divided into two portions. To one of these portions was added a 3% solution'of soap bark extract, sufroom temperature and'coatings which had been aged for three months at room temperature. The following results were obtained.
  • Example 3 The same emulsion used in Example 1 was treated with the spreading agents indicated below and the white (11 A WhlFte Sgots, slghltelspots, 8 ran 11 ant res ay ueu ap g g tion(F.)
  • SMP used in the above examples means the sodium salt of maleopimaric acid.
  • Example 4 In the manner illustrated in Example 1, an ordinary gelatino-silver-chlorobromide emulsion was divided into several batches, and each of these batches treated with a. spreading agent as identified in the table, alone and in combination with tannic acid. The emulsions were then coated on a paper support and processed as described above. The number of white spots per 8" by 10" sheet were measured for the fresh coatings, as well as for the coatings after incubation for eight days at 120 F. and three months storage under room conditions. The number of white spots for each of the coatings is given in the following table.
  • OMT means oleoyl methyl taurine
  • N-methyl-p-aminophenol sulfate 1.5 Sodium sulfite, anhydrous 22.5 Hydroquinone 6.3 Sodium carbonate, anhydrous 15.0 Potassium bromide 1.5
  • Such color couplers include the oil-soluble couplers, such as l-phenyl- ⁇ 3-[2-(2,4diamylphenoxy) -5 (Z-suifobenZamido)benzamido ⁇ -5 pyrazolone.
  • oil-soluble couplers such as l-phenyl- ⁇ 3-[2-(2,4diamylphenoxy) -5 (Z-suifobenZamido)benzamido ⁇ -5 pyrazolone.
  • Such emulsions can contain conventional gelatin hardening agents, such as mucochloric acid, although it has been found that bis-esters of methane sulfonic acid of the type hardening agents are 1,5-di(methane sulfonoxy)-pentano 1,2-di (methane sulfonoxy) ethane, etc.
  • a gelatin coating composition comprising (1) gelatin, (2) a synthetic spreading agent selected from those represented by the following general formula:
  • R-ii-N-CHrOHzSOsM wherein R represents an aliphatic hydrocarbon radical containing at least eight carbon atoms, R represents a. member selected from the group consisting of an aliphatic radical containing one to four carbon atoms, a cycloalkyl group and an aryl group, and M represents a member selected from the group consisting of an alkali metal atom, an ammonium group and an organic ammonium group, and (3) tannic acid.
  • gelatin coating composition comprising (1) gelatin, (2) a synthetic spreading agent selected from those represented by the following general formula:
  • R represents a memberselected from the group consisting of a hydrogen atom, a lower alkyl group, a water-soluble carboxylic acid group and a water-soluble carboxyl alkyl group
  • R represents a member selected from the group consisting of a hydrogen atom and an alkyl group containing from 5 to 18 carbon atoms
  • M represents a water-soluble cation
  • n represents a positive integer of from 1 to 12
  • x represents a positive integer of from 1 to 4, and (3) tannic acid.
  • a gelatin coating composition comprising (1) gelatin, (2) a synthetic spreading agent selected from those represented by the following general formula:
  • R represents an aliphatic hydrocarbon radical containing at least 8 carbon atoms
  • R represents a member selected from the group consisting of a lower alkyl group, a water-soluble carboxylic acid salt group and a water-soluble carboxy alkyl group
  • M represents a watersoluble cation
  • X represents a member selected from the group consisting of a divalent oxygen atom
  • n represents a positive integer of from 1 to 12
  • d represents a positive integer of from 1 to 3
  • tannic acid
  • a gelatin coating composition comprising (1) gelatin, (2) a synthetic spreading agent selected from those represented by the following general formula:
  • R represents a member selected from the group consisting of a lower alkyl group, a water-soluble carboxylic acid salt group, and a water-soluble carboxy alkyl group
  • R represents a member selected from the group consisting of an aliphatic hydrocarbon radical containing at least 8 carbon atoms and an aryl group, the alkyl portion of which contains at least 8 carbon atoms
  • X represents the member selected from the group consisting of a divalent oxygen atom, a -CONHCHgCH30- 7 group and a s-.-O(CH CH group, n represents a positive integer of from 1 to 12, M represents a watersoluble cation and d represents a positive integer of from 1 to 3, and (3) tannic acid.
  • a gelatin coating composition comprising (1) gelatin, (2) oleoyl methyl taurine, and (3) tannic acid.
  • a gelatin coating composition comprising (1) gelatin, (2) sodium maleopimarate, and (3) tannic acid.
  • a gelatin coating composition comprising (1) gelatin, (2) N-(carbo-p-tertiary octyl phenoxy pentaethoxy) glutamate disodium salt, and (3) tannic acid.
  • a gelatin coating composition comprising (1) gelatin, (2) tetrasodium maleopimaroyl glutamate, and (3) tannic acid.
  • a photographic gelatino-silver-halide emulsion comprising (1) a synthetic spreading agent selected from those represented by the following general formula:
  • R represents a member selected from the group consisting of a hydrogen atom, a lower alkyl group, a water-soluble carboxylic acid group and a water-soluble carboxy alkyl group
  • R represents a member selected from the group consisting of a hydrogen atom and an alkyl group containing from 5 to 18 carbon atoms
  • M represents a water-soluble cation
  • n represents a positive integer of from 1 to 12
  • x represents a positive integer of from 1 to 4, and (2) tannic acid.
  • a photographic gelatino-silver-halide emulsion comprising (1) a synthetic spreading agent selected from those represented by the following general formula:
  • R represents an aliphatic hydrocarbon radical containing at least 8 carbon atoms
  • R represents a memher selected from the group consisting of a lower alkyl group, a water-soluble carboxylic acid salt group and a Water-soluble carboxy alkyl group
  • M represents a watersoluble cation
  • X represents a member selected from the group consisting of a divalent oxygen atom, a
  • n represents a positive integer of from 1 to 12
  • :1 represents a positive integer of from 1 to 3
  • (2) tannic acid
  • a photographic gelatino-silverhalide emulsion comprising (1) a synthetic spreading agent selected from those represented by the following general formula:
  • R represents a member selected from the group consisting of a lower alkyl group, a water-soluble carboxylic acid salt group, and a water-soluble carboxy alkyl group
  • R represents a member selected from the group consisting of an aliphatic hydrocarbon radical containing at least 8 carbon atoms and an alkaryl group, the alkyl portion of which contains at least 8 carbon atoms
  • X represents the member selected from the group consisting of a divalent oxygen atom, a
  • a photographic gelatino-silver-halide emulsion containing sodium maleopimarate and tannic acid 14.
  • a photographic gelatino-silver-halide emulsion containing oleoyl methyl taurine and tannic acid 15.

Description

. 1 3,003,877 SPOT PREVENTION IN PHOTOGRAPHIC EMUL- SIONS AND COLLOID LAYERS Leonard T. McLaughlin, Avon, and Bill R. Burks, Rochester, N.Y., assignors to Eastman Kodak Company, Rochester, N.Y., a Corporation of New Jersey No Drawing. Filed June 27, 1957, Ser. No. 668,316
' 16 Claims. (CI. 9694) This invention relates to improved photographic coatings comprising a synthetic spreading agent and tannic acid.
It is known that saponin can be used in gelatin coating compositions for the purpose of obtaining uniform coatings substantially free of bare spots and other surface imperfections. It is also known that commercial saponin varies considerably from batch to batch, such variations making it quite difficult at times to obtain uniform results in the coatings.
It has been previously proposed to replace commercial saponin or soap bark extract with certain synthetic coating aids which can be manufactured to give uniform results in the coatings. For example, Knox et al. U.S. Patent 2,739,891, issued March 27, 1956, describes a class of aminosulfonic acid salts which can be used to replace the conventional saponin coating aid. Other synthetic coating aids are described in Knox et al. U.S. application Serial No. 556,044, filed December 29, 1955; Knox et a1. U.S. application Serial N0. 600,679, filed July 30, 1956, and Wilson et a1. U.S. application Serial No. 603,195, filed August 9, 1956.
While such synthetic coating agents have provided material benefits not obtainable with commercial saponin,
they generally lack certain of the desirable properties contributed by the tannic acid of the extract. Certain photographic coating solutions contain minute metallic iron or iron compounds as impurities and when photographic coatings containing such impurities and the synthetic coating aids are processed in the normal manner, small desensitized areas, or areas of reduced density appear in the course of the process. These small areas of reduced density show up as white spots, thus producing a rather serious defect in the final photographic print.
An effort has been made to overcome the undesirable effect produced by the metallic iron or iron compounds by using various chelating agents, such as derivatives of ethylenediamine tetracetic acid and the like. However, these chclating agents have not been effective in eliminating the small areas of reduced density or white spots. We have found that the aforementioned benefits of the synthetic spreading agents can be retained, while eliminating their serious side effects by adding small amounts of tannic acid to the coating solution. By tannic acid we mean mdigallic acid (approx. C H O M.W=322.23).
It is, therefore, an object of our invention to provide an improved means of obtaining uniform gelatin coatings for photographic use. Another object is to provide a means of avoiding reduced density areas when synthetic spreading agents are used in preparing photographic gelatin coatings. Other objects will become apparent from a consideration of the following examples and description.
We have found that tannic acid can be added directlyv to ordinary gelatino-silver-halide emulsions containing synthetic spreading agents as coating aids, or to other photographic gelatin coating vsolutions containing no light-sensitive material, such as the coatings generally employed in imbibition printing blanks. tannic acid can be added to gelatin Alternatively, the
coating solutions United States Patentp v acid in a layer contiguous to the light-sensitive layer, it
is generally desirable to use a larger quantity of tannic acid in the coating solution.
The synthetic coating aids used as a replacement for commercial saponin are generally compounds containing a hydrophobic moiety, such as a long-chain alkyl group, in combination with a hydrophilic moiety, such as sulfonic acid salt groups or carboxylic acid salt groups. These synthetic coating aids frequently have an amide group somewhere in the chain. These synthetic coating aids can be classified generically as water-soluble salts of sulfonic or carboxylic acids containing an amido group. While representative synthetic coating aids or spreading agents are illustrated below, it is to be understood that other synthetic agents can be employed to equal advantage in accomplishing the beneficial results afiorded by the tannic acid of our invention. Typical coating aids include those represented by the following general formulas:
R-C-N-CHaGHaSOaM E nt-xl-ii-N-omoHio-o-NHdn oHi)d-ioo0M oHioHi0-oNHoH(OHi)d-i 3ooM' l wherein R represents an aliphatic hydrocarbon radical containing at least 8 carbon atoms (e.g., n-octyl, n-decyl, n-myristyl, n-cetyl, oleyl, linoleyl, etc.), R represents an aliphatic radical containing not more than about 4 carbon atoms (e.g., methyl, ethyl, n-propyl, n-butyl, etc.), a cycloalkyl group (e.g., cyclopentyl, cyclohexyl, etc.), or an aryl group (e.g., phenyl, tolyl, etc.), R represents a hydrogen atom, a lower alkyl group (e.g., methyl, ethyl, etc.), a water-soluble carboxylic acid group or a watersoluble carboxyalkyl group (e.g., carboxymethyl, carboxyethyl, etc.), R represents a hydrogen atom or an alkyl group containing at least 5 carbon atoms (e.g.,
'n-amyl, n-octyl, etc., such as alkyl groups containing from 5 to 18 carbon atoms, so that the total number of carbon atoms in the R groups is at least 10)," R represents the carbocyclic nucleus of a rosin acid, such as'rosinyl, hyro- ,rosinyl, dihydrorosinyl, etc., radicals, R represents a lower alkyl group (e.g.,
methyl, ethyl, etc.), an aryl group (e.g., phenyl, tolyl, etc.), a water-soluble carboxylic acid salt group or a water-soluble'salt of a carboxycarboxymethyl, carboXyetl-iyl, etc.), R
at least 8 carbon atoms (such as those radicals listed above with respect to R) or an' alkaryl group, the alkyl portion of which contains at least-8 carbon atoms (e.g.,
O n-octyl, n-decyl, etc.), M represents an alkali metal atom '(e.g., sodium, potassium, etc.), ammonium or organic ammonium (i.e., derivatives where a salt has been formed between the sulfonic acid and an organic amine, such as pyridine, triethylamine, triethanolamine, etc.), n represents a positive integer from 1 to 12, x represents a posisi ese o from 1 o .4, m rep en a pc ti e in of from 1 to 2, d represents a positive integer of from to 3, X p sen s a m t n Q Y r p (-CH2 a me hy ne mi ro p H2 H-) r t e g up -CH O(CH CH O)', where n has the values given ab e. an X1 nts a d len xy n a m. the O( HsCHa)n where n has the values given above.
The synthetic spreading agents represented by Formula 1 above can be prepared as described in US. Patent 2,739,891. Among the useful synthetic spreading agents 'sclosed in the patent are the alkali metal salts of oleoyl methyl taurine.
The synthetic spreading agents represented by Formula II above can be prepared according to the method described in application Serial No. 556,044 mentioned above, as well as US. application Serial No. 600,679. Useful synthetic spreading agents shown in these applications include N-(carbo-p-tertiary octyl phenoxy pentath x glutamate i d m salt, N- ar c-fiamid ethoxy aspartic acid sodium salt, etc.
The synthetic spreading agents represented by Formula III above can be prepared as described in Serial No. 603,195 mentioned above. Typical of such synthetic spreading agents are sodium N-carbo-abityl oxy glutamate, N-carbo-abityl-oxy polyethoxy glycine sodium salt, etc.
The synthetic spreading agents represented by Forinulas IV an'd V above can be prepared as described in Serial No. 600,679 mentioned above. Typical spreading agents include 3,8,l3-triaza-4,l2-dioxo-5,1l-dioxa-S-lauroyl pentadecane-1,l5-dioic acid sodium salt, etc.
Other synthetic spreading agents useful in our invention include the alkali metal salts of maleopimaric acid, which is disclosed in US. Patent 2,628,226. The use of this particular type of synthetic spreading agent is disclosed in Serial No. 556,044 mentioned above.
Other synthetic spreading agents, which can be used in place of saponin to provide the useful results illustrated below, are tetrasodium maleopimaroyl glutamate, tetrasodium maleopimaroyl aspartate and similar maleopimaroyl derivatives of amino aliphatic polycarboxylic acids.
The amounts of synthetic spreading agents useful in our invention are well known to those skilled in the art. The useful amounts of these agents have been previously described in the references referred to above. For example, oleoyl methyl taurine can be used in an amount varying from about .0055 to .5%, based on the amount of dry gelatin in the coating composition. The most useful amount for a given spreading agent can be determined by running a series of test coatings, wherein the amounts of spreading agent are varied. The point at which the uniform spreading occurs without the formation of dry areas in the coating can be readily observed.
In like manner, the amount of tannic acid used in our invention can be varied, depending upon the source of the gelatin, particular spreading agent being used, and the like. In general, we have found that from about .065 gram to .65 gram per 100 Square feet of coated area is sufiicient for the purposes of our invention.
When used in gelatino-silver-halide emulsions, it has been noted that particularly useful results have been obtained with the so-called paper emulsions containing silver chlorobromide. However, other gelatino-silverhalide emulsions, such as silver chloride, silver bromiodide, silver chlorobromicdide, etc. emulsions can also. be treated according to our invention.
The following examples will serve to illustrate more fully the manner of practicing our invention.
sons
Example An ordinary gelatino-silver-chlorobromide emulsion was divided into several batches, and these batches treated with the amounts of tannic acid shown in the following table. Certain of the batches contained sufficient spreading agent to insure uniform coating, these spreading agents being identified in the table. The various emulsions were then coated on an ordinary photographic paper support and the coatings dried and processed in the usual manner. The number of white spots per 8" by 10" sheet were measured for the fresh coatings, as well as for the coatings after incubation for eight days at 120 F. and three months under storage under ambient conditions. The number of white spots for each of the three conditions 1s given in the following table.
Whlte Spreading White Spots, White g.l sq.lt.'1annic acid Agent Spots, 8 day Spots,
Fresh Incuba- 3 Months tion soap bark 2 7 21 .....do. 1% 2 3 1 0 l 1 1 (1 4 35 7B 1% 2 o 2 I5 2 l. l 1 1 1 Extract.
Example 2 The same emulsion batch used in Example 1 above was divided into two portions. To one of these portions was added a 3% solution'of soap bark extract, sufroom temperature and'coatings which had been aged for three months at room temperature. The following results were obtained.
White White White Soap Bark Extract Spots, Spots, Spats,
Fresh 6 Weeks 3 Months 5 1 s 20 as This example shows that some ingredient present in soap bark extract has the property of preventing white spots in photographic paper emulsions during processing. Of course, the coatings of this example suffered from the ordinary defects accompanying the use of commercial saponin.
Example 3 The same emulsion used in Example 1 was treated with the spreading agents indicated below and the white (11 A WhlFte Sgots, slghltelspots, 8 ran 11 ant res ay ueu ap g g tion(F.)
sMP 21 is? Soap bark extract (clarified) v 3 65 Commercial saponln 1 51 Tannic acid can be added to coatings containing clarified soap bark extract to improve the properties of such coatings, insofar as the prevention of white spots during processing is concerned. The following tabulation will show this effect, the number of white spots given in the table being based on an 8" by 10" sheet.
The abbreviation SMP used in the above examples means the sodium salt of maleopimaric acid.
Example 4 In the manner illustrated in Example 1, an ordinary gelatino-silver-chlorobromide emulsion was divided into several batches, and each of these batches treated with a. spreading agent as identified in the table, alone and in combination with tannic acid. The emulsions were then coated on a paper support and processed as described above. The number of white spots per 8" by 10" sheet were measured for the fresh coatings, as well as for the coatings after incubation for eight days at 120 F. and three months storage under room conditions. The number of white spots for each of the coatings is given in the following table.
'Ifngic gvhitte lslllhizte gvhitte S readin A out 01 p s, p0 s, po s p g g g./l06 Fresh 8 dayin- 3mont .5
sq. ft. cubation In the above table, OMT means oleoyl methyl taurine,
G. N-methyl-p-aminophenol sulfate 1.5 Sodium sulfite, anhydrous 22.5 Hydroquinone 6.3 Sodium carbonate, anhydrous 15.0 Potassium bromide 1.5
Water to make 1 liter.
While our invention has been described with reference particularly to gelatino-silver-ha-lide emulsions intended for black-and-white photography, it is to he understood that our invention can also be applied to gelatin compositions intended for use in color photography. Thus, tannic acid can be used in combination with conventional synthetic spreading agents of the type described above, these ingredients being incorporated in a gelatino-si-lverhalide emulsion containing color-forming compounds or couplers. Such couplers are generally non-ditfusing in the photographic treating solutions customarily employed in color photography. Such color couplers include the oil-soluble couplers, such as l-phenyl-{3-[2-(2,4diamylphenoxy) -5 (Z-suifobenZamido)benzamido}-5 pyrazolone. Such emulsions can contain conventional gelatin hardening agents, such as mucochloric acid, although it has been found that bis-esters of methane sulfonic acid of the type hardening agents are 1,5-di(methane sulfonoxy)-pentano 1,2-di (methane sulfonoxy) ethane, etc.
What we claim as our invention and desire secured by Letters Patent of the United States is:
1. A gelatin coating composition comprising (1) gelatin, (2) a synthetic spreading agent selected from those represented by the following general formula:
0 R-ii-N-CHrOHzSOsM wherein R represents an aliphatic hydrocarbon radical containing at least eight carbon atoms, R represents a. member selected from the group consisting of an aliphatic radical containing one to four carbon atoms, a cycloalkyl group and an aryl group, and M represents a member selected from the group consisting of an alkali metal atom, an ammonium group and an organic ammonium group, and (3) tannic acid.
2. A gelatin coating composition comprising (1) gelatin, (2) a synthetic spreading agent selected from those represented by the following general formula:
0 0(CH2CHzOh-i-NHGH-COOM in 3)! wherein R represents a memberselected from the group consisting of a hydrogen atom, a lower alkyl group, a water-soluble carboxylic acid group and a water-soluble carboxyl alkyl group, R represents a member selected from the group consisting of a hydrogen atom and an alkyl group containing from 5 to 18 carbon atoms, M represents a water-soluble cation, n represents a positive integer of from 1 to 12, and x represents a positive integer of from 1 to 4, and (3) tannic acid.
3. A gelatin coating composition comprising (1) gelatin, (2) a synthetic spreading agent selected from those represented by the following general formula:
0 RX1g-NHCH(CHz) dl c 0 0M t wherein R represents an aliphatic hydrocarbon radical containing at least 8 carbon atoms, R represents a member selected from the group consisting of a lower alkyl group, a water-soluble carboxylic acid salt group and a water-soluble carboxy alkyl group, M represents a watersoluble cation, X represents a member selected from the group consisting of a divalent oxygen atom, a
group and a -O(CH CH O),, group, n represents a positive integer of from 1 to 12, and d represents a positive integer of from 1 to 3, and (3) tannic acid.
4. A gelatin coating composition comprising (1) gelatin, (2) a synthetic spreading agent selected from those represented by the following general formula:
wherein R represents a member selected from the group consisting of a lower alkyl group, a water-soluble carboxylic acid salt group, and a water-soluble carboxy alkyl group, R represents a member selected from the group consisting of an aliphatic hydrocarbon radical containing at least 8 carbon atoms and an aryl group, the alkyl portion of which contains at least 8 carbon atoms, X, represents the member selected from the group consisting of a divalent oxygen atom, a -CONHCHgCH30- 7 group and a s-.-O(CH CH group, n represents a positive integer of from 1 to 12, M represents a watersoluble cation and d represents a positive integer of from 1 to 3, and (3) tannic acid.
5. A gelatin coating composition comprising (1) gelatin, (2) oleoyl methyl taurine, and (3) tannic acid.
6. A gelatin coating composition comprising (1) gelatin, (2) sodium maleopimarate, and (3) tannic acid.
7. A gelatin coating composition comprising (1) gelatin, (2) N-(carbo-p-tertiary octyl phenoxy pentaethoxy) glutamate disodium salt, and (3) tannic acid.
8. A gelatin coating composition comprising (1) gelatin, (2) tetrasodium maleopimaroyl glutamate, and (3) tannic acid.
9. A photographic gelatino-silver-halide emulsion comprising (1) a synthetic spreading agent selected from those represented by the following general formula:
I 0 (CHzCHaOh--NH$H.COOM
wherein R represents a member selected from the group consisting of a hydrogen atom, a lower alkyl group, a water-soluble carboxylic acid group and a water-soluble carboxy alkyl group, R represents a member selected from the group consisting of a hydrogen atom and an alkyl group containing from 5 to 18 carbon atoms, M represents a water-soluble cation, n represents a positive integer of from 1 to 12, and x represents a positive integer of from 1 to 4, and (2) tannic acid.
11. A photographic gelatino-silver-halide emulsion comprising (1) a synthetic spreading agent selected from those represented by the following general formula:
wherein R represents an aliphatic hydrocarbon radical containing at least 8 carbon atoms, R represents a memher selected from the group consisting of a lower alkyl group, a water-soluble carboxylic acid salt group and a Water-soluble carboxy alkyl group, M represents a watersoluble cation, X represents a member selected from the group consisting of a divalent oxygen atom, a
group and a -O(CH CH O) group, n represents a positive integer of from 1 to 12, and :1 represents a positive integer of from 1 to 3, and (2) tannic acid.
12. A photographic gelatino-silverhalide emulsion comprising (1) a synthetic spreading agent selected from those represented by the following general formula:
wherein R represents a member selected from the group consisting of a lower alkyl group, a water-soluble carboxylic acid salt group, and a water-soluble carboxy alkyl group, R represents a member selected from the group consisting of an aliphatic hydrocarbon radical containing at least 8 carbon atoms and an alkaryl group, the alkyl portion of which contains at least 8 carbon atoms, X represents the member selected from the group consisting of a divalent oxygen atom, a
CONHCH CH O-- group and a O(CH CH O),, group, n represents a positive integer of from 1 to 12, M represents a watersoluble cation and d represents a positive integer of from 1 to 3, and (2) tannic acid.
13. A photographic gelatino-silver-halide emulsion containing sodium maleopimarate and tannic acid.
14. A photographic gelatino-silver-halide emulsion containing N-(carbo-p-tertiaryoctyl phenoxy pentaethoxy) glutamate disodium salt and tannic acid.
15. A photographic gelatino-silver-halide emulsion containing oleoyl methyl taurine and tannic acid.
16. A photographic gelatino-silver-halide emulsion containing tetrasodium maleopimaroyl glutamate and tannic acid.
References Cited in the file of this patent UNITED STATES PATENTS 2,389,292 Bjorksten Nov. 20, 1945 2,481,650 Fierke Sept. 13, 1949 2,532,390 Bennett et al. Dec. 5, 1950 2,739,891 Knox Mar. 27, 1956 OTHER REFERENCES Sheppard: Gelatin in Photography, vol. 1, 1923, pp. 11 and 12, pub. Van Nostrand Co., NY.
UNITED STATES PATENT OFFICE CERTIFICATION OF CORRECTION Patent No. 3,003,877 October 10 1961 Leonard T, McLaughlin et al.
ppeers in the above numbered pat- It is hereby certified that error a id Letters Patent should read as ent requiring correction and that the sa corrected below.
Column 6, line 72 for "aryl" read alkaryl column 8, lines 14 to 19 the formula should appear as shown below instead of as in the patent:
O I 0 R I! II I cn ca o-fi-matlzmca -cooM Signed and sealed this 17th day of April 1962 (SEAL) Attest:
ESTON G, JOHNSON DAVID L, LADD Commissioner of Patents Attesting Officer

Claims (1)

  1. 9. A PHOTOGRAPHIC GELATINO-SILVER-HALIDE EMULSION COMPRISING (1) A SYNTHETIC SPREADING AGENT SELECTED FROM THOSE REPRESENTED BY THE FOLLOWING GENERAL FORMULA:
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Cited By (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3165409A (en) * 1962-02-07 1965-01-12 Eastman Kodak Co Derivatives of certain highly branched chain acids as coating aids
US3169870A (en) * 1961-12-04 1965-02-16 Eastman Kodak Co Photographic gelatin layers containing the salts of various alkyl and alkenyl succinamates as coating aids
US3663229A (en) * 1966-10-12 1972-05-16 Agfa Gevaert Nv Photographic elements containing carboxyalkyl polyglycol ethers and esters
US3769022A (en) * 1969-12-31 1973-10-30 Agfa Gevaert Nv Photosensitive silver halide emulsions comprising coating aids
US3778268A (en) * 1969-05-28 1973-12-11 Konishiroku Photo Ind Light-sensitive silver halide photographic material
US3907573A (en) * 1970-08-21 1975-09-23 Minnesota Mining & Mfg Silver halide photographic emulsions with improved physical characteristics
USD979656S1 (en) 2020-12-11 2023-02-28 Kids Ii Hape Joint Venture Limited Toy drum
USD985677S1 (en) 2021-01-11 2023-05-09 Kids Ii Hape Joint Venture Limited Toy guitar

Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2389292A (en) * 1945-02-08 1945-11-20 Bjorksten Johan Preparation of protein compositions and masses having improved physical characteristics
US2481650A (en) * 1948-01-10 1949-09-13 Eastman Kodak Co Removing soluble salts from photographic emulsions
US2532390A (en) * 1945-05-28 1950-12-05 Preparation of a printing surface
US2739891A (en) * 1953-07-17 1956-03-27 Eastman Kodak Co Method of preparing photographic products

Patent Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2389292A (en) * 1945-02-08 1945-11-20 Bjorksten Johan Preparation of protein compositions and masses having improved physical characteristics
US2532390A (en) * 1945-05-28 1950-12-05 Preparation of a printing surface
US2481650A (en) * 1948-01-10 1949-09-13 Eastman Kodak Co Removing soluble salts from photographic emulsions
US2739891A (en) * 1953-07-17 1956-03-27 Eastman Kodak Co Method of preparing photographic products

Cited By (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3169870A (en) * 1961-12-04 1965-02-16 Eastman Kodak Co Photographic gelatin layers containing the salts of various alkyl and alkenyl succinamates as coating aids
US3165409A (en) * 1962-02-07 1965-01-12 Eastman Kodak Co Derivatives of certain highly branched chain acids as coating aids
US3663229A (en) * 1966-10-12 1972-05-16 Agfa Gevaert Nv Photographic elements containing carboxyalkyl polyglycol ethers and esters
US3778268A (en) * 1969-05-28 1973-12-11 Konishiroku Photo Ind Light-sensitive silver halide photographic material
US3769022A (en) * 1969-12-31 1973-10-30 Agfa Gevaert Nv Photosensitive silver halide emulsions comprising coating aids
US3907573A (en) * 1970-08-21 1975-09-23 Minnesota Mining & Mfg Silver halide photographic emulsions with improved physical characteristics
USD979656S1 (en) 2020-12-11 2023-02-28 Kids Ii Hape Joint Venture Limited Toy drum
USD985677S1 (en) 2021-01-11 2023-05-09 Kids Ii Hape Joint Venture Limited Toy guitar

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