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Publication numberUS2566263 A
Publication typeGrant
Publication dateAug 28, 1951
Filing dateDec 19, 1947
Priority dateAug 30, 1945
Also published asUS2566245
Publication numberUS 2566263 A, US 2566263A, US-A-2566263, US2566263 A, US2566263A
InventorsSmith William F, Trivelli Adrian P H
Original AssigneeEastman Kodak Co
Export CitationBiBTeX, EndNote, RefMan
External Links: USPTO, USPTO Assignment, Espacenet
Stabilizing photographic emulsions with chloropalladites and chloroplatinites
US 2566263 A
Abstract  available in
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Claims  available in
Description  (OCR text may contain errors)

Patented Aug. 28, 1951 ST'AEILIZING rnorrodngi nio iifMULfsi'oNs WITH CHLOROPALLADITES. AND" CHLORO- PLATiNITEs Adrian P. H. Trivelliand William-F. Smith-Rochester, N.;Y., assignors to Eastman Kodak Company, Rochester, N. Y., acorporation of New Jersey No Drawing. Applicationfiecmber 19, 1947,

Serial No. 7925842 7 4 Claims.

This invention relates to fog-inhibiting agents and stabilizers for photographic emulsions and to photographic emulsions containing them.

This application is a continuation-impart of our application Serial No. 687,239, filed July 30,

1946, now abandoned. It is known that photo-x graphic emulsions, particularly ultra-sensitive emulsions or those containing coloring serisitiz'ers exhibit a tendency to form a deposit of silver in the'emulsion. This deposit extendsmore' or less uniformly over the entire emulsion and is known as fog. Photographic fog is of two types: local and general. Local fog is formed by exposure of the film or plate at undesired points as by a little leak in the camera. General fog orasit is some- (ores-i) adverse conditions of temperature and humidity by the use of compounds of the formulas:

R'zMXi' and R3MX6 'in R is hydrogen or an 2.1km metai in cl'iiding" ammonium, M is'platinum or palladi M" is iridium or rhodium and is ahawgem Compounds suitable for use according" toour invention are those of :the abovegeneralformulas in which R is hydrogen or an alkali metal such as potassium or sodium, or ammonium; M

platinum or palladium; M is iridium or rhodium;

and X is a halogen atom such as chier nexor times known chemical fog is formed in a number of ways. It may be caused by the conditions under which the film or plate is stored, such as conditions of high temperature or humidity or unusually long time of storage; The" nature of the emulsion may also produce chemical fogas br'omirie; Suitable compounds are ammonium chloropalladite, (NH4)2(PdC14) ammonium chloroplatinite (NI-I4) zPtCli; ammonium chloroiridite 1 (NHLQBIICIQ and ammonium chlororhodite well as the conditions of development of the emulsion as by development for protracted periods of time or at temperatures above. normal. Highly sensitive emulsions are more likely to fog than those of lower sensitivity. wears primarily concerned with general or chemicaliog.

of silver halide emulsions at or close to initial optimum values under conditions of high temperature and humidity. Thefog inhibitors which we propose to use are added to the emulsion General fog and loss of sensitivity of the emulsion are especially likely occur when the sensitive material is stored under conditions other than ideal, that is, under conditions of high temperature and humidity as tropical regions.

It is an object of the invention to provide novel anti-fogging or fog-inhibiting compounds for emulsions. A further object is to provideantifogging agents which stabilize the initial sensitivity of the emulsion. A still further" object is to provide anti-fogging agents which improve the keeping of the emulsion in. tropical regions. Other objects will appear from the followingdescription of our invention.

In our prior application, Serial No. 765,818Lfi1ed August '2, 1947, We described the use as foginhibitors of compounds of the general formula:

of which ammonium ohloropalladate is aneuample. We have now foundthat the sensitivity d fog of nhotqgraphic mul iee may em mw tained at or'close to initial optimum values'under during" the process of manufacture to avoid-lossof sensitivityfand to inhibit' thef growth of chem'a-g ical fog withpassage of time under non-ideal con j ditioiis of storage. Theseconditions freque exist where photographic emulsionsare' used tropical countries or on naval vessels or manufacturing plafits'wlie're adverse keeping conditions" prevail. The advantages of our discovery reside a widerange of climatic conditions.

A solution of ammonium chlorop-alladite or a other fog inhibitor used according to our invention, when added in suitable concentration lie" 40.

unsensitized or optically sensitized photograph emulsions before coating, does not eifecttlie sen-Q sitometric values for sensitivity and fog when.

measurements are made soon after coating.

When sensitcmetric masurements are mad}; after appreeiame intervals of time under tropical 6r dry conditions or storage at elevated tempera:

tures, however, these compounds do" stabilize plie tcgraphic speed andina'i'ntain reg at a' iewiev The preparation of s'iwr halide exams-ion in volves three separate operations (l') theemulsiii By the use of the compounds oi our invention, it is possible to maintain the sensitivity and fog.

3 cation 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 in- The fog inhibiting agents which we have described may be used in various kinds of photographic emulsions. In addition to being useful in ordinary non-sensitized emulsions, they may also creased e v y e y Of the 5 be used in ortho-chromatic, panchromatic and Photographic P 1912)- We prefer to add X-ray emulsions. If used with sensitizing dyes, h f nhi n mp n af r the final they may be added to the emulsion before or digestion after-ripening, although they may after the dyes are added. Various silver salts may be added prior to the fin e p- Useful be used as the-sensitive salt, such as silver broconcentrations are from 0.25 to .9 gram o o mide, silver iodide, silver chloride and mixtures inhibitor per kilogram of silver nitrate converted of t Th dispersing agents may be gelatin to Silver halide in ma t emlllSiOIl- "or other colloid, such as collodion, alubumen, The fog inhibiting d Stabilizing action of 0111 cellulose organic derivatives or synthetic resins. compounds was determined by incubation of the t 1 be understood t t we contemplate as emulsions with simulated tropical conditions an 5 included within our invention all modifications also y incubation in dry heat at and equivalents falling Within the scope of the apous lengths of time from 12 days to 2 months. pended 1 The results of these tests are tabulated below and w claim; are compared with the initial Speed, gamma and 1. A stabilized silver halide emulsion containfog of the emulsions with and Withou? the Stabi' ing silver halide as the sole sensitive ingredient 112mg compounfi- The tests from Whlcl} the and containing from 0.25 gram to 3.9 grams per IOWmg tabulatlon was made used a hlgh'speed kilogram of silver nitrate converted to silver negative silver halide emulslon exposed on an halide in making the emulsion, f a compound Eastman type IIB sensitometer and developed for having the Structure five minutes in a developer of the following composition: R2MX4 Grams where R is selected from the group consisting of Monomethyl paramtnophenol Sulfate ydrogen, alkali metals and ammonium, M is sesodium White (desmcated) 30 lected from the group consisting of platinum and g i 3 palladium and X is a halogen atom. gg i g z i gfi g 0 5 2. A. stabilized gelatino-silver halide emulsion Water to one liter containing sliver halide as the sole sensitive ingredient and containing from 0.25 gram to 3.9 The results are as follows: grams per kilogram of silver nitrate converted to Routine 12 da. at 120 F. 8 wks. Tropical V (N HdlalPdgh grams g. g ig 5 Gamma Fog ig Gamma Fog ig Gamma Fog Routine 12 da. at 120 F 8 wks Tropical (NHmPtghfigroam PM g a ig Q Gamma Fog ig 5 Gamma Fog i g Gamma Fog Routine 12 (is. at 120 F 8 wks Tropical (N H1) QIIOIQ gram per kg'AgN ig Gamma Fog ig h Gamma Fog ig Gamma Fog None 710 1.48 .08 300 1.51 is 193 1.34 .41 .434 890 1.35 .10 575 1.29 .20 198 1,40 .30 1,380 1.17 .11 490 1.33 .22 218 1. 39 .31 935 1.35 .10 535 1.30 20 210 1. 30 .30 370 1.39 .09 343 1.40 19 153 1.37 .52

The fog inhibiting agents of our invention are useful principally with emulsions which are desflverhhahde m gmkmg the emulslon' of ammom' veloped with organic developing agents not conum c taining metals. Such developing agents are hygelatmo'snver hahde 82311151011 droquinone, para aminophenol and its deriva containing silver halide as the sole sensitive intives, pyrogallol, paraphenylenediamine and its gredlent and 00111121111112 from gram to 3.9 derivatives, phenylhydroxylamine, etc. grams per kilogram of silver nitrate converted to silver halide in making the emulsion, of ammonium chloroplatinite.

4. The method of stabilizing the speed and reducing the amount of fog produced upon development of a silver halide emulsion containingisilver halide as the sole sensitive ingredient, which comprises incorporating in said emulsion from 0.25 gram to 3.9 grams per kilogram of silver nitrate converted to silver halide in making the emulsion, of a compound having the structure where X is a halogen atom, R is selected from the group consisting of hydrogen, alkali metals and ammonium, and M is selected from the group 15 1,120,580

. 6 consisting of platinum and palladium, and developing said emulsion after exposure with an organic developing agent free of a metallic element.

ADRIAN P. H. TRIVELLI. WILLIAM F. SMITH.

REFERENCES CITED The following references are of record in the file of this patent:

UNITED STATES PATENTS Number I Name Date 1,120,429 Willis Dec. 8, 1914 Willis Dec. :8, 1914

Patent Citations
Cited PatentFiling datePublication dateApplicantTitle
US1120429 *Jun 2, 1914Dec 8, 1914William WillisProcess for the production of photographic prints.
US1120580 *Sep 22, 1913Dec 8, 1914William WillisSensitive photographic paper and process of making the same.
Referenced by
Citing PatentFiling datePublication dateApplicantTitle
US3508925 *Sep 8, 1967Apr 28, 1970Eastman Kodak CoMethod for preparing gelatino emulsions containing latexes and polyvalent salts and products obtained thereby
US4102312 *Oct 30, 1975Jul 25, 1978Toyota Jidosha Kogyo Kabushiki KaishaThermally developable light-sensitive materials
US4617258 *Mar 25, 1986Oct 14, 1986Konishiroku Photo Industry Co., Ltd.Silver halide photographic material
US4892808 *May 12, 1989Jan 9, 1990Eastman Kodak CompanyPhotographic material protected against hydrogen cyanide gas
US4902611 *Jan 6, 1989Feb 20, 1990Leubner Ingo HPreparation of silver halide emulsions containing iridium
US5314670 *Oct 30, 1991May 24, 1994Eastman Kodak CompanyRecovery of rhodium values
US5492803 *Jan 6, 1995Feb 20, 1996Minnesota Mining And Manufacturing CompanyHydrazide redox-dye-releasing compounds for photothermographic elements
US5492804 *Jun 30, 1994Feb 20, 1996Minnesota Mining And Manufacturing CompanyChromogenic leuco redox-dye-releasing compounds for photothermographic elements
US5492805 *Jun 30, 1994Feb 20, 1996Minnesota Mining And Manufacturing CompanyBlocked leuco dyes for photothermographic elements
US5582957 *Mar 28, 1995Dec 10, 1996Eastman Kodak CompanyResuspension optimization for photographic nanosuspensions
US5696289 *Nov 16, 1995Dec 9, 1997Minnesota Mining And Manufacturing CompanyBlocked leuco dyes for photothermographic elements
US5705676 *Nov 16, 1995Jan 6, 1998Minnesota Mining And Manufacturing CompanyChromogenic leuco redox-dye-releasing compounds for photothermographic elements
US5891615 *Apr 8, 1997Apr 6, 1999Imation Corp.Chemical sensitization of photothermographic silver halide emulsions
US5928857 *Dec 18, 1996Jul 27, 1999Minnesota Mining And Manufacturing CompanyPhotothermographic element with improved adherence between layers
US5939249 *Jun 24, 1997Aug 17, 1999Imation Corp.Photothermographic element with iridium and copper doped silver halide grains
US6060231 *Mar 22, 1999May 9, 2000Eastman Kodak CompanyPhotothermographic element with iridium and copper doped silver halide grains
US6117624 *Aug 24, 1999Sep 12, 2000Eastman Kodak CompanyInfrared sensitized, photothermographic article
US6197485 *Sep 27, 1993Mar 6, 2001Minnesota Mining & Manufacturing CompanyPhotographic assemblage comprising a silver halide photographic element sealed in a closed vessel
US7163785Nov 20, 2002Jan 16, 2007Konica Minolta Photo Imaging, Inc.Silver halide photosensitive material and image forming method therefor
US7524621Sep 21, 2007Apr 28, 2009Carestream Health, Inc.Method of preparing silver carboxylate soaps
US7622247Jan 14, 2008Nov 24, 2009Carestream Health, Inc.Protective overcoats for thermally developable materials
EP0124795A2Apr 11, 1984Nov 14, 1984Fuji Photo Film Co., Ltd.Silver halide photographic emulsion
WO1989012847A1 *Jun 12, 1989Dec 28, 1989Eastman Kodak CoPhotographic material protected against hydrogen cyanide gas
WO2012035314A1Sep 7, 2011Mar 22, 2012Fujifilm Imaging Colorants LimitedPhotographic paper
Classifications
U.S. Classification430/448, 430/608
International ClassificationG03C1/09
Cooperative ClassificationG03C1/09
European ClassificationG03C1/09