US3904415A - Phosphine sensitized photographic silver halide emulsions and elements - Google Patents
Phosphine sensitized photographic silver halide emulsions and elements Download PDFInfo
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- US3904415A US3904415A US492956A US49295674A US3904415A US 3904415 A US3904415 A US 3904415A US 492956 A US492956 A US 492956A US 49295674 A US49295674 A US 49295674A US 3904415 A US3904415 A US 3904415A
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- Prior art keywords
- silver halide
- emulsion
- phosphine
- photographic
- tris
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- 239000000839 emulsion Substances 0.000 title claims abstract description 132
- -1 silver halide Chemical class 0.000 title claims abstract description 104
- XYFCBTPGUUZFHI-UHFFFAOYSA-N Phosphine Chemical compound P XYFCBTPGUUZFHI-UHFFFAOYSA-N 0.000 title claims abstract description 101
- 229910052709 silver Inorganic materials 0.000 title claims abstract description 101
- 239000004332 silver Substances 0.000 title claims abstract description 101
- 229910000073 phosphorus hydride Inorganic materials 0.000 title claims abstract description 54
- PCHJSUWPFVWCPO-UHFFFAOYSA-N gold Chemical compound [Au] PCHJSUWPFVWCPO-UHFFFAOYSA-N 0.000 claims abstract description 24
- 229910052737 gold Inorganic materials 0.000 claims abstract description 24
- 239000010931 gold Substances 0.000 claims abstract description 24
- 230000001235 sensitizing effect Effects 0.000 claims abstract description 23
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims abstract description 22
- 229910052717 sulfur Inorganic materials 0.000 claims abstract description 22
- 239000011593 sulfur Substances 0.000 claims abstract description 22
- 239000007983 Tris buffer Substances 0.000 claims abstract description 18
- 238000000576 coating method Methods 0.000 claims description 13
- 239000011248 coating agent Substances 0.000 claims description 12
- 125000004432 carbon atom Chemical group C* 0.000 claims description 11
- 150000003003 phosphines Chemical class 0.000 claims description 11
- 150000001875 compounds Chemical class 0.000 claims description 10
- FDIOSTIIZGWENY-UHFFFAOYSA-N n-[bis(diethylamino)phosphanyl]-n-ethylethanamine Chemical compound CCN(CC)P(N(CC)CC)N(CC)CC FDIOSTIIZGWENY-UHFFFAOYSA-N 0.000 claims description 7
- 230000003595 spectral effect Effects 0.000 claims description 6
- URQFNWOYQMPPKL-UHFFFAOYSA-N n-bis(dibutylamino)phosphanyl-n-butylbutan-1-amine Chemical compound CCCCN(CCCC)P(N(CCCC)CCCC)N(CCCC)CCCC URQFNWOYQMPPKL-UHFFFAOYSA-N 0.000 claims description 4
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical group [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims 2
- 125000004663 dialkyl amino group Chemical group 0.000 abstract description 3
- 239000010410 layer Substances 0.000 description 9
- 239000000126 substance Substances 0.000 description 9
- 125000000217 alkyl group Chemical group 0.000 description 7
- 229910052698 phosphorus Inorganic materials 0.000 description 7
- 235000014786 phosphorus Nutrition 0.000 description 7
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 description 6
- 206010070834 Sensitisation Diseases 0.000 description 6
- 239000011574 phosphorus Substances 0.000 description 6
- 230000008313 sensitization Effects 0.000 description 6
- BQCADISMDOOEFD-UHFFFAOYSA-N Silver Chemical compound [Ag] BQCADISMDOOEFD-UHFFFAOYSA-N 0.000 description 4
- 238000010348 incorporation Methods 0.000 description 4
- 238000000034 method Methods 0.000 description 4
- BASFCYQUMIYNBI-UHFFFAOYSA-N platinum Chemical compound [Pt] BASFCYQUMIYNBI-UHFFFAOYSA-N 0.000 description 4
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- 230000000052 comparative effect Effects 0.000 description 3
- 238000011161 development Methods 0.000 description 3
- 150000003018 phosphorus compounds Chemical class 0.000 description 3
- 238000002360 preparation method Methods 0.000 description 3
- ADZWSOLPGZMUMY-UHFFFAOYSA-M silver bromide Chemical compound [Ag]Br ADZWSOLPGZMUMY-UHFFFAOYSA-M 0.000 description 3
- RIOQSEWOXXDEQQ-UHFFFAOYSA-N triphenylphosphine Chemical class C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1 RIOQSEWOXXDEQQ-UHFFFAOYSA-N 0.000 description 3
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 2
- 108010010803 Gelatin Proteins 0.000 description 2
- KDLHZDBZIXYQEI-UHFFFAOYSA-N Palladium Chemical compound [Pd] KDLHZDBZIXYQEI-UHFFFAOYSA-N 0.000 description 2
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 2
- ORILYTVJVMAKLC-UHFFFAOYSA-N adamantane Chemical group C1C(C2)CC3CC1CC2C3 ORILYTVJVMAKLC-UHFFFAOYSA-N 0.000 description 2
- 125000002947 alkylene group Chemical group 0.000 description 2
- 239000003795 chemical substances by application Substances 0.000 description 2
- 239000000975 dye Substances 0.000 description 2
- 229920000159 gelatin Polymers 0.000 description 2
- 239000008273 gelatin Substances 0.000 description 2
- 235000019322 gelatine Nutrition 0.000 description 2
- 235000011852 gelatine desserts Nutrition 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- 229910052697 platinum Inorganic materials 0.000 description 2
- 239000011591 potassium Substances 0.000 description 2
- 229910052700 potassium Inorganic materials 0.000 description 2
- 150000003839 salts Chemical class 0.000 description 2
- ZUNKMNLKJXRCDM-UHFFFAOYSA-N silver bromoiodide Chemical compound [Ag].IBr ZUNKMNLKJXRCDM-UHFFFAOYSA-N 0.000 description 2
- 239000003381 stabilizer Substances 0.000 description 2
- CWGBFIRHYJNILV-UHFFFAOYSA-N (1,4-diphenyl-1,2,4-triazol-4-ium-3-yl)-phenylazanide Chemical compound C=1C=CC=CC=1[N-]C1=NN(C=2C=CC=CC=2)C=[N+]1C1=CC=CC=C1 CWGBFIRHYJNILV-UHFFFAOYSA-N 0.000 description 1
- DZKXDEWNLDOXQH-UHFFFAOYSA-N 1,3,5,2,4,6-triazatriphosphinine Chemical compound N1=PN=PN=P1 DZKXDEWNLDOXQH-UHFFFAOYSA-N 0.000 description 1
- JAAIPIWKKXCNOC-UHFFFAOYSA-N 1h-tetrazol-1-ium-5-thiolate Chemical class SC1=NN=NN1 JAAIPIWKKXCNOC-UHFFFAOYSA-N 0.000 description 1
- OWIRCRREDNEXTA-UHFFFAOYSA-N 3-nitro-1h-indazole Chemical class C1=CC=C2C([N+](=O)[O-])=NNC2=C1 OWIRCRREDNEXTA-UHFFFAOYSA-N 0.000 description 1
- 101100391545 Mus musculus Fxyd3 gene Proteins 0.000 description 1
- KFVIGFHJAWWJDZ-UHFFFAOYSA-N N-butyl-N-phosphanylbutan-1-amine Chemical compound C(CCC)N(CCCC)P KFVIGFHJAWWJDZ-UHFFFAOYSA-N 0.000 description 1
- 238000001016 Ostwald ripening Methods 0.000 description 1
- 239000002202 Polyethylene glycol Substances 0.000 description 1
- BUGBHKTXTAQXES-UHFFFAOYSA-N Selenium Chemical compound [Se] BUGBHKTXTAQXES-UHFFFAOYSA-N 0.000 description 1
- 229910021607 Silver chloride Inorganic materials 0.000 description 1
- ZMZDMBWJUHKJPS-UHFFFAOYSA-M Thiocyanate anion Chemical compound [S-]C#N ZMZDMBWJUHKJPS-UHFFFAOYSA-M 0.000 description 1
- SJOOOZPMQAWAOP-UHFFFAOYSA-N [Ag].BrCl Chemical compound [Ag].BrCl SJOOOZPMQAWAOP-UHFFFAOYSA-N 0.000 description 1
- HOLVRJRSWZOAJU-UHFFFAOYSA-N [Ag].ICl Chemical compound [Ag].ICl HOLVRJRSWZOAJU-UHFFFAOYSA-N 0.000 description 1
- PXBKYPOTLZKEFR-UHFFFAOYSA-N [Au].[S].P Chemical compound [Au].[S].P PXBKYPOTLZKEFR-UHFFFAOYSA-N 0.000 description 1
- 125000003545 alkoxy group Chemical group 0.000 description 1
- 238000013459 approach Methods 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- 125000004429 atom Chemical group 0.000 description 1
- 125000002091 cationic group Chemical group 0.000 description 1
- 239000000084 colloidal system Substances 0.000 description 1
- 229940000425 combination drug Drugs 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 230000000593 degrading effect Effects 0.000 description 1
- 230000008021 deposition Effects 0.000 description 1
- 230000029087 digestion Effects 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 239000007888 film coating Substances 0.000 description 1
- 238000009501 film coating Methods 0.000 description 1
- 230000006870 function Effects 0.000 description 1
- 150000002343 gold Chemical class 0.000 description 1
- 229910001385 heavy metal Inorganic materials 0.000 description 1
- XMBWDFGMSWQBCA-UHFFFAOYSA-N hydrogen iodide Chemical compound I XMBWDFGMSWQBCA-UHFFFAOYSA-N 0.000 description 1
- ZMZDMBWJUHKJPS-UHFFFAOYSA-N hydrogen thiocyanate Natural products SC#N ZMZDMBWJUHKJPS-UHFFFAOYSA-N 0.000 description 1
- 239000011229 interlayer Substances 0.000 description 1
- 239000000314 lubricant Substances 0.000 description 1
- 150000002730 mercury Chemical class 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 125000000325 methylidene group Chemical group [H]C([H])=* 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 239000003607 modifier Substances 0.000 description 1
- XVDBWWRIXBMVJV-UHFFFAOYSA-N n-[bis(dimethylamino)phosphanyl]-n-methylmethanamine Chemical compound CN(C)P(N(C)C)N(C)C XVDBWWRIXBMVJV-UHFFFAOYSA-N 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 150000002923 oximes Chemical class 0.000 description 1
- 229910052763 palladium Inorganic materials 0.000 description 1
- 150000002941 palladium compounds Chemical class 0.000 description 1
- AQSJGOWTSHOLKH-UHFFFAOYSA-N phosphite(3-) Chemical class [O-]P([O-])[O-] AQSJGOWTSHOLKH-UHFFFAOYSA-N 0.000 description 1
- 150000004714 phosphonium salts Chemical class 0.000 description 1
- PTMHPRAIXMAOOB-UHFFFAOYSA-N phosphoramidic acid Chemical compound NP(O)(O)=O PTMHPRAIXMAOOB-UHFFFAOYSA-N 0.000 description 1
- 125000004437 phosphorous atom Chemical group 0.000 description 1
- 239000004014 plasticizer Substances 0.000 description 1
- 229920001223 polyethylene glycol Polymers 0.000 description 1
- 239000004848 polyfunctional curative Substances 0.000 description 1
- 235000020004 porter Nutrition 0.000 description 1
- 238000012545 processing Methods 0.000 description 1
- 229910052711 selenium Inorganic materials 0.000 description 1
- 239000011669 selenium Substances 0.000 description 1
- HKZLPVFGJNLROG-UHFFFAOYSA-M silver monochloride Chemical compound [Cl-].[Ag+] HKZLPVFGJNLROG-UHFFFAOYSA-M 0.000 description 1
- AKHNMLFCWUSKQB-UHFFFAOYSA-L sodium thiosulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=S AKHNMLFCWUSKQB-UHFFFAOYSA-L 0.000 description 1
- 235000019345 sodium thiosulphate Nutrition 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- 150000003464 sulfur compounds Chemical class 0.000 description 1
- DHCDFWKWKRSZHF-UHFFFAOYSA-N sulfurothioic S-acid Chemical compound OS(O)(=O)=S DHCDFWKWKRSZHF-UHFFFAOYSA-N 0.000 description 1
- 150000003498 tellurium compounds Chemical class 0.000 description 1
- 150000003568 thioethers Chemical class 0.000 description 1
- UMGDCJDMYOKAJW-UHFFFAOYSA-N thiourea Chemical class NC(N)=S UMGDCJDMYOKAJW-UHFFFAOYSA-N 0.000 description 1
- 238000012546 transfer Methods 0.000 description 1
Classifications
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- 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
- G03C1/28—Sensitivity-increasing substances together with supersensitising substances
-
- 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
- G03C1/10—Organic substances
-
- Y—GENERAL 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
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S430/00—Radiation imagery chemistry: process, composition, or product thereof
- Y10S430/151—Matting or other surface reflectivity altering material
Definitions
- a photographic silver halide emulsion is disclosed incorporating a sensitizing amount of a tris(dialkylamino)-phosphine or a tris(dialkylaminoalkylene)- phosphine.
- Gold and/or sulfur sensitizers can also be present as well as antifoggants, such as azaindenes.
- phosphorus compounds While varied phosphorus containing compounds have been recognized to be sensitizers for photographic silver halide emulsions, it should not be assumed that phosphorus compounds are, in general, useful as silver halide sensitizers. Phosphorus compounds, in fact, cover the full gamut of performance characteristics, ranging from densensitizers to sensitizers. Even among those classes of phosphorus compounds known to be sensitizers unexplained variations in performance are observable.
- One difficulty with many phosphorus sensitizers has been their ineffectiveness and/or incompatibility with other chemical sensitizers. For example, some phosphorus sensitizers in combination with heavy metal sensitizers, such as gold sensitizers, produce no additional speed increase while others produce prohibitively large increases in fog.
- phosphine compounds to be useful as sensitizers for silver halide emulsions. More surprisingly I have found these compounds to be capable of producing additional increases in photographic speed when employed in combination with conventional chemical sensitizers. Still further, silver halide emulsions containing these compounds as sensitizers either alone or in combination with other chemical sensitizers show surprisingly low fog levels. By contrast, I have observed distinctly inferior comparative performance for certain closely related and homologous phosphine compounds.
- my invention is directed to a photographic silver halide emulsion comprised of silver halide grains, a vehicle for dispersing said grains and a sensitizing amount of a tri(dialkylamino)phosphine or a tri(dialkylaminoalkylcne )phosphine in which each of the alkyl groups contains at least two carbom atoms and each alkylene group contains from one to three carbon atoms.
- my invention is directed to a photographic element incorporating such a photographic emulsion.
- the phosphine compounds which I employ in the practice of my invention are those having three dialkylamino groups attached directly to the phosphorus atom or through an intervening methylene linkage of up to three carbon atoms.
- the alkyl groups can be independently chosen, but in each instance include at least two carbon atoms.
- Preferred phosphine compounds of this type are those represented by the following structural formula:
- R and R are alkyl groups having from 2 to 8 carbon atoms, preferably 2 to 5 carbon atoms, and n is an integer of from 0 to 3 inclusive.
- Exemplary preferred phosphine compounds useful in the practice of this invention are set forth in Table I.
- the silver halide emulsions used in accordance with the sensitizers of my invention can comprise, for example, silver chloride, silver bromide, silver bromoiodide, silver chlorobromide, silver chloroiodide, silver chlorobromoiodide and mixtures thereof.
- the emulsions can be coarse or fine grain emulsions prepared by any of the well-known techniques, e.g., single jet emulsions, such as those described in Trivelli and Smith, The Photographic Journal, Vol. LXXIX, May, 1939 (pp 330-338); double jet emulsions, such as those described in Glafkides, Photographic Chemistry, Vol.
- the silver halide emulsions utilized in this invention can be surface sensitized and/or internally sensitized.
- One convenient approach for forming internally sensitized emulsions is to sensitize the grain surfaces of an emulsion to be employed as a core emulsion followed by the further deposition of silver halide on the sensitized surfaces of the grains.
- Exemplary of internal image forming silver halide emulsions which can be used in the practice of this invention with phosphine sensitizers are those sensitized predominantly on the interior of the silver halide grains as described in Porter et al. US. Pat. No. 3,206,313, issued Sept. 14, 1965; Porter et a1.
- the silver halide emulsions can be regular grain emulsions such as the type described in Klein and Moisar, J. Plml. S011, Vol. 12, No. 5, Sept./Oct., 1964, pp 242251 and German Patent 2,107,] 18.
- Negative type emulsions can be utilized, as well as direct-positive emulsions described in lllingsworth U.S. Pat. No. 3,501,307, issued Mar. 17, 1970 and Berriman US, Pat. No. 3,367,778, issued Feb. 6, 1968', such emulsions being surface fogged in addition to being internally sensitized.
- silver halide emulsions employed in the practice of my invention are preferably chemically sensitized according to conventional practice in addition to including the phosphine sensitizers.
- My silver halide emulsions can be usefully sensitized with chemical sensitizers, such as with sulfur, selenium or tellurium compounds; gold, platinum or palladium compounds; or combinations of these. Procedures for chemically sensitizing silver halide emulsions are described in Sheppard et al. US. Pat. No. 1,623,499, issued Apr. 15, 1927; Waller et a1.
- My phosphine sensitizers can be added in a variety of ways to photographic emulsions and at various stages in the preparation thereof; however, I prefer to introduce the phosphine sensitizers of my invention immediately after chemical sensitization by conventional techniques has been completed and before other addenda have been incorporated into the emulsion.
- the sensitizers can be added with useful effects at the completion of Ostwald ripening and prior to one or more of the final digestion operations.
- the sensitizers are preferably added to the silver halide emulsion after the silver halide grains are substantially in their final size and shape.
- the phosphine sensitizers can be added in methanol,
- the silver halide emulsion not be maintained above a temperature of about 50 to C for an extended period in preparation steps subsequent to phosphine incorporation.
- Effective phosphine sensitization can be obtained by holding the emulsion at an elevated temperature of up to about 40C or more for a period ranging from a few minutes to an hour or" more-preferably 10 to 40 minutes.
- any sensitizing amount of the phosphine compounds of this invention can be usefully incorporated into the silver halide emulsion. Typically concentrations of from about 0.1 to mg of phosphine sensitizer per mole of silver halide, preferably 0.5 to 50 mg of phosphine sensitizer per mole of silver halide, can be employed.
- the maximum concentrations of the phosphine sensitizers is a function of (a) the amount of background fog compatible with the particular photographic application and (b) whether or not an antifoggant is incorporated in the silver halide emulsion. While the phosphine sensitizers are generally compatible with known antifoggants and stabilizers, I have found the phosphine sensitizers employed in the practice of this invention to be particularly effective in combination with known azaindene antifoggants, most preferably tetrazaindene antifoggants. Exemplary antifoggants and stabilizers, each used alone or in combination include the following:
- the silver halide emulsions include a vehicle for dispersing the silver halide grains.
- the vehicle is typically a hydrophilic colloid, such as gelatin, but can take any conventional form.
- the silver halide emulsion can contain any one or a variety of conventional photographic emulsion addenda, such as hardeners, spectral sensitizers, brighteners, coating aids, plasticizers and lubricants, absorbing and filter dyes, developing agents, development modifiers, etc.
- Typical conventional vehicles and addenda of this type useful in the practice of this invention are disclosed in Product Licensing Index, Vol. 92, December 1971, publication 9232, pages 107 through 1 10, here incorporated by reference.
- the photographic emulsions according to my invention can be employed as coatings in single and multilayer photographic elements. Such elements typically include a conventional photographic support of the type disclosed specifically in paragraph X of Product Licensing Index, cited above.
- the photographic emulsion layers can be employed in combination with subbing, interlayers, Carey Lea silver layers, antihalation layers, etc., as is well understood in the art.
- the photographic elements according to my invention can be applied to a variety of applications.
- the photographic elements can be used with X-rays or can be orthochromatic, panchromatic or infrared sensitive.
- the photographic elements can be employed to form black-and-white images or to form colored or multicolored images in one or a plurality of layers as taught specifically in paragraph XXll of Product Licensing Indcx, cited above.
- the photographic elements can be of a type which form images upon development in conventional silver halide developing solutions, which form images by dry physical development, which form images by image transfer, etc.
- the photographic elements can be employed as lithographic printing plates as taught in paragraph XXIV of Product Licensing Index, cited above.
- the photographic elements can be formed to produce positive or negative images and can be formed to be of the direct print type, as specifically disclosed in paragraph XXV of Product Licensing Index, cited above.
- a silver bromide emulsion having a mean grain size of 0.4 micron in diameter was prepared using a conventional double jet technique.
- the emulsion was separated into equal portions and chemically sensitized to a maximum obtainable speed using none, one, or a combination of the sulfur sensitizer sodium thiosulfate and- /or the gold sensitizer potassium chloraurate, as shown below in Table 11.
- the emulsion samples were finished as shown in Table 11, and the phosphine compound was then added as a coating addenda at the concentration shown in Table 11.
- the phosphine sensitizer was added at 40C and the emulsion sample was held at this temperature for 20 minutes.
- the emulsion samples were then coated on a film support at 20 mg silver per square decimeter, exposed, developed for 4 minutes in Kodak Developer D-19 (the composition of which is set forth at page 43 of Kodak Advanced Data Book .l-l, titled Processing Chemicals and Formulas for Black-and- White Photography, 6th edition, published 1963), fixed, washed and dried.
- Kodak Developer D-19 the composition of which is set forth at page 43 of Kodak Advanced Data Book .l-l, titled Processing Chemicals and Formulas for Black-and- White Photography, 6th edition, published 1963
- Example 1 in comparing Example 1 with Control 1 it is apparent that the phosphine sensitizer more than doubled the speed of the emulsion.
- Example 2 and 3 in comparing Examples 2 and 3 with Controls 2 and 3 it is apparent that the phosphine sensitizer in combination with the sulfer sensitizer produced an emulsion more than 3 times faster than the emulsion containing the sulfur sensitizer alone.
- the phosphine sensitizer PS-3 increased fog by 0.01 or less in all instances, even when TABLE [1 Fin. Conditions Fresh Sensitizers (mg/Ag mole) Time Temp. Relative Example No. Phosphine Sulfur Gold (Minutes) (C] Speed Gamma Fog Control-l None None None 20 40 100 3.1 0.04 l 30 (PS-3) None None 20 40 224 3.4 0.04 Contro
- the emulsion was separated into equal portions, and phosphine compounds as set forth in Table IV were added to separate portions.
- the emulsion portions were at 55C at the time the phosphine compound was added and were then reduced in temperature to 40C and held for minutes. The results are summarized below in Table IV.
- a photographic silver halide emulsion comprising photographic silver halide grains, a vehicle for dispersing said silver halide grains and a sensitizing amount of a tris(dialkylamino)phosphine or a tris(dialkylaminoalkylene )phosphine in which each of the alkyl groups contain at least two carbon atoms and the alkylene group contains from one to three carbon atoms.
- a photographic silver halide emulsion comprising a sensitizing amount of a compound of the formula wherein R and R are alkyl groups having from 2 to 8 carbon atoms and n is an integer of from 0 to 3.
- a photographic silver halide emulsion comprising photographic silver halide grains
- a photographic element comprised of a sup port and, as a coating on said support, a layer com prised of a photographic silver halide emulsion, the improvement in which said photographic silver halide emulsion is defined by claim 1.
- said silver halide emulsion is additionally sensitized with gold sensitizing means, sulfur sensitizing means or a combination of gold and sulfur sensitizing means.
- a photographic element comprised of a support and, as a coating on said support, a layer comprised of a photographic silver halide emulsion
- said emulsion is comprised of a sensitizing amount of a compound of the formula NqCH n wherein R and R are alkyl groups having from 2 to 5 carbon atoms and n is O or 1
- said emulsion additionally includes a amount of gold sensitizing means.
- a photographic element according to claim 16 the further improvement in which said emulsion contains a sensitizing amount of at least one of tris(diethylamino)phosphine, tris(dibutylamino)phosphine or tris(diethylaminomethylene) phosphinel 18.
- said phosphine sensitizer is present in an amount of from 0.1 to 100 mg per mole of silver halide.
- a photographic element comprised of a support and, as a coating on said support, a layer comprised ofa photographic silver halide emulsion, the imsensitizing provement in which said emulsion contains from 0.5 to 50 mg per mole of silver halide of tris(diethylamino)- phosphine.
- a photographic element comprised of a support and, as a coating on said support, a layer comprised ofa photographic silver halide emulsion, the improvement in which said emulsion contains from 0.5 to 50 mg per mole of silver halide of tris(di-nbutylamino )phosphine.
- a photographic element comprised of a support and, as a coating on said support, a layer comprised ofa photographic silver halide emulsion, the improvement in which said emulsion contains from 0.5 to 50 mg per mole of silver halide of tris( diethylaminomethylene )phosphine.
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- Chemical & Material Sciences (AREA)
- Spectroscopy & Molecular Physics (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- General Physics & Mathematics (AREA)
- Silver Salt Photography Or Processing Solution Therefor (AREA)
Abstract
A photographic silver halide emulsion is disclosed incorporating a sensitizing amount of a tris(dialkylamino)-phosphine or a tris(dialkylaminoalkylene)phosphine. Gold and/or sulfur sensitizers can also be present as well as antifoggants, such as azaindenes.
Description
United States Patent [1 1 Ottedahl [451 Sept. 9, 1975 I PHOSPHINE SENSITIZED PHOTOGRAPHIC SILVER HALIDE EMULSIONS AND ELEMENTS [75] Inventor: Edwin N. Oftedahl, Rochester, NY.
[73] Assignee: Eastman Kodak Company,
Rochester, NY.
[22] Filed: July 29, 1974 [21] Appl No.: 492,956
FOREIGN PATENTS OR APPLICATIONS 1,295,463 11/1972 United Kingdom 96/107 195,872 7/1967 U.S.S.R 96/107 OTHER PUBLICATIONS Stauebe et al.: J. Am. Chem. Soc., Vol. 78, pages 976-977 (1956).
Primary Examiner-Won H. Louie, Jr. Attorney, Agent, or Firm-C. 0. Thomas 5 7 ABSTRACT A photographic silver halide emulsion is disclosed incorporating a sensitizing amount of a tris(dialkylamino)-phosphine or a tris(dialkylaminoalkylene)- phosphine. Gold and/or sulfur sensitizers can also be present as well as antifoggants, such as azaindenes.
21 Claims, No Drawings PHOSPHINE SENSITIZED PHOTOGRAPHIC SILVER HALIDE EMULSIONS AND ELEMENTS My invention relates to phosphine sensitized silver halide emulsions which can be further sensitized with chemical sensitizers and to photographic elements including such emulsions.
The use of phosphorus and its compounds as sensitizers for photographic silver halide emulsions and elements is known in the art. For example, British Patent 1,057,949, published Feb. 18, 1967, teaches the sensitization of silver bromide emulsions by developing in the presence of an amido-phosphoric acid polyethylene glycol ester. British Patent [295,463, published Nov. 8, 1972, teaches that silver halide emulsions can be sensitized through the use of gelatin which has been treated with phosphine or white phosphorus. Thurston US. Pat. No. 3,338.712, issued Aug. 29, l967, teaches sensitizing emulsions containing labile sulfur compounds by the incorporation of organic phosphites. Carroll et al. US. Pat. No. 2,27l,622, issued Feb. 3, 1942, teaches the sensitization of silver halide emulsions using cationic surface-active phosphonium salts. Lowe et al. US. Pat. No. 3,523,023, issued Aug. 4, 1970, teaches the sensitization of silver halide emulsions with hydroxyalkyl phosphonium salts. Willems et al U.S. Pat. No. 3,552,968, issued Jan. 5, 1971, teaches sensitization with phosphonitrile trimer and tetramer derivatives. Russian Patent l95,872, published July 1 l, 1967, discloses to be sensitizers for silver halide emulsions triphenyl phosphines, including those having alkyl, aryl, alkoxy or dialkylamino phenyl substituents.
While varied phosphorus containing compounds have been recognized to be sensitizers for photographic silver halide emulsions, it should not be assumed that phosphorus compounds are, in general, useful as silver halide sensitizers. Phosphorus compounds, in fact, cover the full gamut of performance characteristics, ranging from densensitizers to sensitizers. Even among those classes of phosphorus compounds known to be sensitizers unexplained variations in performance are observable. One difficulty with many phosphorus sensitizers has been their ineffectiveness and/or incompatibility with other chemical sensitizers. For example, some phosphorus sensitizers in combination with heavy metal sensitizers, such as gold sensitizers, produce no additional speed increase while others produce prohibitively large increases in fog.
I have discovered quite unexpectedly a class of phosphine compounds to be useful as sensitizers for silver halide emulsions. More surprisingly I have found these compounds to be capable of producing additional increases in photographic speed when employed in combination with conventional chemical sensitizers. Still further, silver halide emulsions containing these compounds as sensitizers either alone or in combination with other chemical sensitizers show surprisingly low fog levels. By contrast, I have observed distinctly inferior comparative performance for certain closely related and homologous phosphine compounds.
In one aspect then, my invention is directed to a photographic silver halide emulsion comprised of silver halide grains, a vehicle for dispersing said grains and a sensitizing amount of a tri(dialkylamino)phosphine or a tri(dialkylaminoalkylcne )phosphine in which each of the alkyl groups contains at least two carbom atoms and each alkylene group contains from one to three carbon atoms. In another aspect, my invention is directed to a photographic element incorporating such a photographic emulsion.
My invention may be better understood and appreciated by reference to the following detailed description:
The phosphine compounds which I employ in the practice of my invention are those having three dialkylamino groups attached directly to the phosphorus atom or through an intervening methylene linkage of up to three carbon atoms. The alkyl groups can be independently chosen, but in each instance include at least two carbon atoms.
Preferred phosphine compounds of this type are those represented by the following structural formula:
ii- (CH P wherein, R and R are alkyl groups having from 2 to 8 carbon atoms, preferably 2 to 5 carbon atoms, and n is an integer of from 0 to 3 inclusive.
Exemplary preferred phosphine compounds useful in the practice of this invention are set forth in Table I. The first two phosphine compounds listed in Table I, though closely structurally related to those that follow, form no part of my invention, but are included solely for purposes of comparison.
'IABLEEL l tr iphenyl phosphine tris{ dime Lhylainino lpnosphine tris din octylaminomethylene)phosphine The preparation of compounds of this type is generally well known in the art. For example, an exemplarly technique suitable for preparing these compounds is disclosed by Carl Stauebe and Herman P. Lankelma in J. Am. Chem. Soc, Volume 78, pages 976 through 977 (1956), in an article entitled Hexaalkyl Phosphoru Phosphoric and Phosphoricthioic Triamides."
The silver halide emulsions used in accordance with the sensitizers of my invention can comprise, for example, silver chloride, silver bromide, silver bromoiodide, silver chlorobromide, silver chloroiodide, silver chlorobromoiodide and mixtures thereof. The emulsions can be coarse or fine grain emulsions prepared by any of the well-known techniques, e.g., single jet emulsions, such as those described in Trivelli and Smith, The Photographic Journal, Vol. LXXIX, May, 1939 (pp 330-338); double jet emulsions, such as those described in Glafkides, Photographic Chemistry, Vol. 1, Chapter 28, Fountain Press, London, 1958; ammoniacal, thiocyanate or thioether ripened emulsions such as those described in Nietz et a1. U.S. Pat. No. 2,222,264, issued Nov. 19, 1940; lllingsworth U.S. Pat. No. 3,320,069, issued May 16, 1967 and Jones U.S. Pat. No. 3,574,628, issued Apr. 13, 1971.
The silver halide emulsions utilized in this invention can be surface sensitized and/or internally sensitized. One convenient approach for forming internally sensitized emulsions is to sensitize the grain surfaces of an emulsion to be employed as a core emulsion followed by the further deposition of silver halide on the sensitized surfaces of the grains. Exemplary of internal image forming silver halide emulsions which can be used in the practice of this invention with phosphine sensitizers are those sensitized predominantly on the interior of the silver halide grains as described in Porter et al. US. Pat. No. 3,206,313, issued Sept. 14, 1965; Porter et a1. U.S. Pat. No. 3,317,322, issued May 2, 1967; Spence et al. U.S. Pat. No. 3,690,891, issued Sept. 12, 1972; and Evans U.S. Pat. No. 3,761,276, issued Sept. 25, 1973.
The silver halide emulsions can be regular grain emulsions such as the type described in Klein and Moisar, J. Plml. S011, Vol. 12, No. 5, Sept./Oct., 1964, pp 242251 and German Patent 2,107,] 18. Negative type emulsions can be utilized, as well as direct-positive emulsions described in lllingsworth U.S. Pat. No. 3,501,307, issued Mar. 17, 1970 and Berriman US, Pat. No. 3,367,778, issued Feb. 6, 1968', such emulsions being surface fogged in addition to being internally sensitized.
Inasmuch as the phosphine sensitizers of my inven tion produce further enhanced photographic speeds when employed in combination with known chemical sensitizers, silver halide emulsions employed in the practice of my invention are preferably chemically sensitized according to conventional practice in addition to including the phosphine sensitizers. My silver halide emulsions can be usefully sensitized with chemical sensitizers, such as with sulfur, selenium or tellurium compounds; gold, platinum or palladium compounds; or combinations of these. Procedures for chemically sensitizing silver halide emulsions are described in Sheppard et al. US. Pat. No. 1,623,499, issued Apr. 15, 1927; Waller et a1. U.S. Pat. No. 2,399,083, issued Apr. 23, 1946; McVeigh U.S. Pat. No. 3,297,447, issued Jan. 10, 1967, and Dunn U.S. Pat. No. 3,297,446, issued Jan. 10, 1967.
My phosphine sensitizers can be added in a variety of ways to photographic emulsions and at various stages in the preparation thereof; however, I prefer to introduce the phosphine sensitizers of my invention immediately after chemical sensitization by conventional techniques has been completed and before other addenda have been incorporated into the emulsion. The sensitizers can be added with useful effects at the completion of Ostwald ripening and prior to one or more of the final digestion operations. The sensitizers are preferably added to the silver halide emulsion after the silver halide grains are substantially in their final size and shape.
The phosphine sensitizers can be added in methanol,
acetone or other innocuous organic solvents. To avoid thermally degrading the phosphine sensitizers it is generally preferred that the silver halide emulsion not be maintained above a temperature of about 50 to C for an extended period in preparation steps subsequent to phosphine incorporation. Effective phosphine sensitization can be obtained by holding the emulsion at an elevated temperature of up to about 40C or more for a period ranging from a few minutes to an hour or" more-preferably 10 to 40 minutes.
Any sensitizing amount of the phosphine compounds of this invention can be usefully incorporated into the silver halide emulsion. Typically concentrations of from about 0.1 to mg of phosphine sensitizer per mole of silver halide, preferably 0.5 to 50 mg of phosphine sensitizer per mole of silver halide, can be employed.
Since higher concentrations of the phosphine sensitizers can raise fog levels, the maximum concentrations of the phosphine sensitizers is a function of (a) the amount of background fog compatible with the particular photographic application and (b) whether or not an antifoggant is incorporated in the silver halide emulsion. While the phosphine sensitizers are generally compatible with known antifoggants and stabilizers, I have found the phosphine sensitizers employed in the practice of this invention to be particularly effective in combination with known azaindene antifoggants, most preferably tetrazaindene antifoggants. Exemplary antifoggants and stabilizers, each used alone or in combination include the following:
a. thiazolium salts described in Brooker et al. US. Pat. No. 2,131,038, issued Sept. 27, 1938 and Allen et a1. U.S. Pat. No. 2,694,716, issued Nov, 16, 1954;
b. the azaindenes described in Piper US, Pat. No. 2,886,437, issued May 12, 1959 and Heimbach et al. US. Pat. No. 2,444,605, issued July 6, 1948;
c. the mercury salts as described in Allen et a1. U.S. Pat No. 2,728,633, issued Dec. 27, 1955;
d. the urazoles described in Anderson et al. U.S. Pat.
No. 3,287,135, issued Nov. 22, 1966',
e. the sulfocutechols described in Kennard et a1. U.S. Pat No. 3,326,652, issued Feb. 22, 1966;
f. the oximes described in Carroll et al. British Patent 623,448, issued May 18, 1949',
g. nitron;
h. nitroindazoles',
i. mercaptotetrazoles described in Kendall et al. U.S. Pat. No. 2,403,927, issued July 16, 1946; Kennard et al. U.S. Pat. No. 3,266,897, issued Aug. 16, 1966', and Luckey et al. U.S. Pat. 3,397,987, issued Aug. 20, 1968;
j. the polyvalent metal salts described in Jones U.S. Pat. No. 2,829,405, issued June 17, 1958;
k. the thiuronium salts described in Herz et a1. U.S. Pat. No. 3,220,839, issued Nov. 30, 1965; and
l. the palladium, platinum and gold salts described in Trivelli et al. U.S. Pat. No. 2,566,263, issued Aug. 28, 1951; and Yutzy et al. U.S. Pat. No. 2,597,915, issued May 27, 1952.
In addition to the components above mentioned the silver halide emulsions include a vehicle for dispersing the silver halide grains. The vehicle is typically a hydrophilic colloid, such as gelatin, but can take any conventional form. In addition, the silver halide emulsion can contain any one or a variety of conventional photographic emulsion addenda, such as hardeners, spectral sensitizers, brighteners, coating aids, plasticizers and lubricants, absorbing and filter dyes, developing agents, development modifiers, etc. Typical conventional vehicles and addenda of this type useful in the practice of this invention are disclosed in Product Licensing Index, Vol. 92, December 1971, publication 9232, pages 107 through 1 10, here incorporated by reference.
The photographic emulsions according to my invention can be employed as coatings in single and multilayer photographic elements. Such elements typically include a conventional photographic support of the type disclosed specifically in paragraph X of Product Licensing Index, cited above. The photographic emulsion layers can be employed in combination with subbing, interlayers, Carey Lea silver layers, antihalation layers, etc., as is well understood in the art.
The photographic elements according to my invention can be applied to a variety of applications. The photographic elements can be used with X-rays or can be orthochromatic, panchromatic or infrared sensitive. The photographic elements can be employed to form black-and-white images or to form colored or multicolored images in one or a plurality of layers as taught specifically in paragraph XXll of Product Licensing Indcx, cited above. The photographic elements can be of a type which form images upon development in conventional silver halide developing solutions, which form images by dry physical development, which form images by image transfer, etc. The photographic elements can be employed as lithographic printing plates as taught in paragraph XXIV of Product Licensing Index, cited above. The photographic elements can be formed to produce positive or negative images and can be formed to be of the direct print type, as specifically disclosed in paragraph XXV of Product Licensing Index, cited above.
The following examples are intended to further illustrate my invention.
EXAMPLES 1 THROUGH 10 A silver bromide emulsion having a mean grain size of 0.4 micron in diameter was prepared using a conventional double jet technique. The emulsion was separated into equal portions and chemically sensitized to a maximum obtainable speed using none, one, or a combination of the sulfur sensitizer sodium thiosulfate and- /or the gold sensitizer potassium chloraurate, as shown below in Table 11. The emulsion samples were finished as shown in Table 11, and the phosphine compound was then added as a coating addenda at the concentration shown in Table 11. The phosphine sensitizer was added at 40C and the emulsion sample was held at this temperature for 20 minutes. The emulsion samples were then coated on a film support at 20 mg silver per square decimeter, exposed, developed for 4 minutes in Kodak Developer D-19 (the composition of which is set forth at page 43 of Kodak Advanced Data Book .l-l, titled Processing Chemicals and Formulas for Black-and- White Photography, 6th edition, published 1963), fixed, washed and dried.
in comparing Example 1 with Control 1 it is apparent that the phosphine sensitizer more than doubled the speed of the emulsion. In comparing Examples 2 and 3 with Controls 2 and 3 it is apparent that the phosphine sensitizer in combination with the sulfer sensitizer produced an emulsion more than 3 times faster than the emulsion containing the sulfur sensitizer alone. Comparing Examples 4, 5 and 6 with Controls 4, 5 and 6, adding the phosphine sensitizer to the sulfur and gold sensitized emulsion produced a greater than two-fold speed increase. Finishing the sulfur and gold sensitized emulsions improved speed, but was not essential to achieving further speed increases with the phosphine sensitizers. The phosphine sensitizer PS-3 increased fog by 0.01 or less in all instances, even when TABLE [1 Fin. Conditions Fresh Sensitizers (mg/Ag mole) Time Temp. Relative Example No. Phosphine Sulfur Gold (Minutes) (C] Speed Gamma Fog Control-l None None None 20 40 100 3.1 0.04 l 30 (PS-3) None None 20 40 224 3.4 0.04 Contro|2 None 6.0 None 3 3.4 0.04 2 30 (PS-3) 6.0 None 3 75 363 3.4 0.04 Control-3 None 6.0 None 30 75 l4l 4.3 0.04 3 30 (PS-3) 6.0 None 30 75 575 4.5 0.04 Control-4 None 3.0 3.0 0 75 468 3.2 0.04 4 3 (PS-3) 3.0 3.0 0 75 I260 2.9 0.05 Control-5 None 3.0 3.0 30 75 l 100 3.2 0.06 5 3 (PS3) 3.0 3 0 30 75 2190 3.3 0.07 Control-6 None None 3.0 K 75 490 2. l 0.13 (1 3 (PS3) None 3.1) 8 75 H00 1.6 0.]4
TABLE ll-continucd Fin. Conditions Fresh Sensitizers (mg/Ag mole) Time Temp. Relative Example No. Phosphine Sulfur Gold (Minutes) (T) Speed Gamma Fog Control-7.8 None 3.0 l.(] 5 75 725 3. 2 [L06 7 3 (P83) 3.0 l.(J 5 75 I260 2.6 0.06
8 3 (PS-7) 3.0 l.(] 5 75 lSSU 3.0 0.24 Control-LN! None 3.0 l.() 30 75 l IOU 2.6 0.08 9 3 (PS3) 31) l.() 30 75 l7OU 2.7 0.08 ll] 3 (PS-7) 3.0 l.(] 31) 75 l7RU 3.0 (H7 employed in combination with the gold sensitizer. While the phosphine sensitizer PS-7 in combination with the sulfur and gold sensitizer increased fog, this was by less than 0.20 and therefore clearly acceptable for many photographic applications.
EXAMPLES ll THROUGH 26 certain of the samples as indicated in Table [ll followed by holding for l0 minutes at C. An antifoggant, 4- hydroxy-o-methyl-l,3,3a,7-tetrazaindene, was then added to certain of the emulsion samples, as indicated in Table [I]. The emulsion samples were coated as in Example I. A portion of each film coating was exposed on an Eastman 1B sensitometer through a continuous step wedge and through either a Wratten 35 38A (Blue) filter or a Wratten l6 (Minus Blue) filter and processed as in Example 1. The results, summarized in Table lll. show that both the blue and minus blue speeds of the spectrally sensitized silver halide emulsions are enhanced by the phosphine sensitizers of this invention used in combination with sulfur and gold sensitizers. Fog levels are not prohibitively high without the antifoggant being present, but are reduced to very low levels through the incorporation of the antifoggant.
TABLE [II Relative Rel. Minus Example Phosphine Cmpd. Spectral Sens. Antifoggant Blue Blue Gamma Fog No. mg/Ag mole mg/Ag mole g/Ag mole Speed Speed [Blue/Minus Blue] Control-l l None None None lUO l.6/* (llO/Ullli Control-l 2 None 2 HKA] ZHB] None ll() lOtl 2.()/2.l (].(J7/ll.[l7 ControH 3 None 2IU(AJ 21(8) 2.95 l 10 I07 2.0/2.7 ODS/0.08 l 1 (PS3) L3 None None 2(19 l.3/* O.l l/l].l() l2 (PS-3) 1.3 None 2.95 182 l.S/* 006/0116 I] (PS3) 1.3 2l()(A)+2l(B) None I35 95 l.6/l.7 O.l(]/0.IU l4 (PS-3] l.3 210(A) 2|(B) 2.95 l 148 l.7/l.8 (109/009 15 (PS3) [.U None None 209 l.4/* (l. l 0/1). l0 l6 (PS-3) l.l| None 2.95 l74 l.5/* O.(l6/U.l)fi l7 (PS-3) l.(] ZHHA) +2l(B| None I35 ll5 l.7/l.8 (J.O9/(l.l)9 l8 (PS-3) l.(l 2lll(A] 'i-ZHB) 2.95 [48 l32 l.7/l.7 (109/009 Control-1 4 None None None I (it) l.4/* 008/008 l9 (PS-5| l5 None 2.95 257 l.3/* 0.2 U022 20 (PS-5) 15 None 2.95 246 l.6/* 010/0. 1U 21 (PS-5) 30 None None 269 l.4/* U.4l/().4tl 2.! (PS-5) 30 None 2.95 282 l.S/* [).l(l/().ll ControIlS None 386(C) 33(D) None Hi5 l(lU l.3/l.3 (LOB/0.08 Controldh None 386(C) 33( D) 2.95 I29 l l 5 l.5/l.7 (lilo/0.06 23 (PS-5) l5 386((1 +33(D) None I4] I26 l.4/l.7 (129/028 24 (PS-5) 15 386((] 33( D] 2.95 148 l4l l.3/l.4 (lilo/(1.26 :5 (PS-5) 30 386K) 33 D None ll() I15 0.8/0.9 0.581055 26 [PS5] 30 386(C) 33(D) 295 Ml l4] L01] .0 OAK/(L55 Not A licable EXAMPLES 27 AND 28 A silver bromoiodide emulsion containing 6 mole percent iodide was chemically sensitized to a maximum attainable speed using 12.0 mg of soidum thiosulfate and 4.4 mg of potassium chloroaurate per mole of silver. The emulsion was separated into equal portions, and phosphine compounds as set forth in Table IV were added to separate portions. The emulsion portions were at 55C at the time the phosphine compound was added and were then reduced in temperature to 40C and held for minutes. The results are summarized below in Table IV.
in comparing Control 17 with the Comparative Examples employing triphenyl phosphine and tris(dimethylamino)phosphine, it is apparent that the properties of the emulsions are only marginally modified, if at all, by the incorporation of these phosphine compounds. On the other hand, when the phosphine sensitizer of this invention, tris( diethylamino)phosphine, is incorporated in the emulsion a very significant increase in the relative blue speed is apparent. This result could not be predicted from the comparative examples.
In addition to the phosphorus containing sensitizers disclosed herein, I have also discovered phosphorus imides of adamantane structure to be useful chemical sensitizers. These are disclosed in my commonly assigned, concurrently filed US. patent application Ser. No. 492,792, titled SILVER HALIDE EMULSIONS AND ELEMENTS INCLUDING SENSITIZERS OF ADA MANTANE STRUCTURE.
The invention has been described with particular reference to preferred embodiments thereof but it will be understood that variations and modifications can be effected within the spirit and scope of the invention.
I claim:
1. A photographic silver halide emulsion comprising photographic silver halide grains, a vehicle for dispersing said silver halide grains and a sensitizing amount of a tris(dialkylamino)phosphine or a tris(dialkylaminoalkylene )phosphine in which each of the alkyl groups contain at least two carbon atoms and the alkylene group contains from one to three carbon atoms.
2. A photographic silver halide emulsion according to claim 1, in which said emulsion is additionally sensitizcd with a gold sensitizer, a sulfur sensitizer or a com bination of gold and sulfur sensitizers.
3. A photographic silver halide emulsion according to claim 2 in which said emulsion additionally includes an antifoggant.
4. A photographic silver halide emulsion according to claim 2 in which said emulsion additionally includes at least one spectral sensitizer.
5. A photographic silver halide emulsion comprising a sensitizing amount of a compound of the formula wherein R and R are alkyl groups having from 2 to 8 carbon atoms and n is an integer of from 0 to 3.
6. A photographic silver halide emulsion according to claim 5 in which n is O or 1.
7. A photographic silver halide emulsion according to claim 5 in which said emulsion is additionally sensitized with a gold sensitizer, a sulfur sensitizer or a combination of gold and sulfur sensitizers.
8. A photographic silver halide emulsion according to claim 7 in which said emulsion additionally includes an azaindene antifoggant.
9. A photographic silver halide emulsion according to claim 8 in which said emulsion additionally includes a spectral sensitizing dye.
10. A photographic silver halide emulsion according to claim 5 in which R and R' each contain from 2 to 5 carbon atoms.
11. A photographic silver halide emulsion according to claim 1 in which said phosphine sensitizer is present in an amount of from 0.1 to mg per mole of silver halide.
12. A photographic silver halide emulsion comprising photographic silver halide grains,
a vehicle for dispersing said silver halide grains and from 0.5 to 50 mg per mole of silver halide of tris(- diethylamino )phosphine tris( di-n-butylamino phosphine, tris(diethylaminomethylene)phosphine or a combination of at least two of said phosphines.
13. [n a photographic element comprised of a sup port and, as a coating on said support, a layer com prised of a photographic silver halide emulsion, the improvement in which said photographic silver halide emulsion is defined by claim 1.
14. in a photographic element according to claim 13 the further improvement in which said silver halide emulsion is additionally sensitized with gold sensitizing means, sulfur sensitizing means or a combination of gold and sulfur sensitizing means.
15. In a photographic element according to claim 14 the further improvement in which said emulsion includes antifoggant means.
16. In a photographic element comprised of a support and, as a coating on said support, a layer comprised of a photographic silver halide emulsion, the improvement in which said emulsion is comprised of a sensitizing amount of a compound of the formula NqCH n wherein R and R are alkyl groups having from 2 to 5 carbon atoms and n is O or 1, and said emulsion additionally includes a amount of gold sensitizing means.
17. In a photographic element according to claim 16, the further improvement in which said emulsion contains a sensitizing amount of at least one of tris(diethylamino)phosphine, tris(dibutylamino)phosphine or tris(diethylaminomethylene) phosphinel 18. [n a photographic element according to claim 13, the further improvement in which said phosphine sensitizer is present in an amount of from 0.1 to 100 mg per mole of silver halide.
19. In a photographic element comprised of a support and, as a coating on said support, a layer comprised ofa photographic silver halide emulsion, the imsensitizing provement in which said emulsion contains from 0.5 to 50 mg per mole of silver halide of tris(diethylamino)- phosphine.
20. In a photographic element comprised of a support and, as a coating on said support, a layer comprised ofa photographic silver halide emulsion, the improvement in which said emulsion contains from 0.5 to 50 mg per mole of silver halide of tris(di-nbutylamino )phosphine.
21. In a photographic element comprised of a support and, as a coating on said support, a layer comprised ofa photographic silver halide emulsion, the improvement in which said emulsion contains from 0.5 to 50 mg per mole of silver halide of tris( diethylaminomethylene )phosphine.
Claims (21)
1. A PHOTORGRAPHIC SILVER HALIDE EMULSION COMPRISING PHOTOGRAPHIC SILVER HALIDE GRAINS, A VEHICLE FOR DISPERSING SAID SILVER HALIDE GRAINS AND A SENSITIZING AMOUNT OF A TRIS(DIALKYLAMINO)PHOTSPHINE OR A TRIS(DIALKYLAMINOALKYLENE) PHOSPHINE IN WHICH EACH OF THE ALKYL GROUPS CONTAIN AT LEAST TWO CARBON ATOMS AND THE ALKYLENE GROUP CONTAINS FROM ONE TO THREE CARBON ATOMS.
2. A photographic silver halide emulsion according to claim 1, in which said emulsion is additionally sensitized with a gold sensitizer, a sulfur sensitizer or a combination of gold and sulfur sensitizers.
3. A photographic silver halide emulsion according to claim 2 in which said emulsion additionally includes an antifoggant.
4. A photographic silver halide emulsion according to claim 2 in which said emulsion additionally includes at least one spectral sensitizer.
5. A photographic silver halide emulsion comprising a sensitizing amount of a compound of the formula
6. A photographic silver halide emulsion according to claim 5 in which n is 0 or 1.
7. A photographic silver halide emulsion according to claim 5 in which said emulsion is additionally sensitized with a gold sensitizer, a sulfur sensitizer or a combination of gold and sulfur sensitizers.
8. A photographic silver halide emulsion according to claim 7 in which said emulsion additionally includes an azaindene antifoggant.
9. A photographic silver halide emulsion according to claim 8 in which said emulsion additionally includes a spectral sensitizing dye.
10. A photographic silver halide emulsion according to claim 5 in which R and R'' each contain from 2 to 5 carbon atoms.
11. A photographic silver halide emulsion according to claim 1 in which said phosphine sensitizer is present in an amount of from 0.1 to 100 mg per mole of silver halide.
12. A photographic silver halide emulsion comprising photographic silver halide grains, a vehicle for dispersing said silver halide grains and from 0.5 to 50 mg per mole of silver halide of tris(diethylamino)phosphine, tris(di-n-butylamino)phosphine, tris(diethylaminomethylene)phosphine or a combination of at least two of said phosphines.
13. In a photographic element comprised of a support and, as a coating on said support, a layer comprised oF a photographic silver halide emulsion, the improvement in which said photographic silver halide emulsion is defined by claim 1.
14. In a photographic element according to claim 13 the further improvement in which said silver halide emulsion is additionally sensitized with gold sensitizing means, sulfur sensitizing means or a combination of gold and sulfur sensitizing means.
15. In a photographic element according to claim 14 the further improvement in which said emulsion includes antifoggant means.
16. In a photographic element comprised of a support and, as a coating on said support, a layer comprised of a photographic silver halide emulsion, the improvement in which said emulsion is comprised of a sensitizing amount of a compound of the formula
17. In a photographic element according to claim 16, the further improvement in which said emulsion contains a sensitizing amount of at least one of tris(diethylamino)phosphine, tris(dibutylamino)phosphine or tris(diethylaminomethylene) phosphine.
18. In a photographic element according to claim 13, the further improvement in which said phosphine sensitizer is present in an amount of from 0.1 to 100 mg per mole of silver halide.
19. In a photographic element comprised of a support and, as a coating on said support, a layer comprised of a photographic silver halide emulsion, the improvement in which said emulsion contains from 0.5 to 50 mg per mole of silver halide of tris(diethylamino)phosphine.
20. In a photographic element comprised of a support and, as a coating on said support, a layer comprised of a photographic silver halide emulsion, the improvement in which said emulsion contains from 0.5 to 50 mg per mole of silver halide of tris(di-n-butylamino)phosphine.
21. In a photographic element comprised of a support and, as a coating on said support, a layer comprised of a photographic silver halide emulsion, the improvement in which said emulsion contains from 0.5 to 50 mg per mole of silver halide of tris(diethylaminomethylene)phosphine.
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CA228,974A CA1037761A (en) | 1974-07-29 | 1975-06-10 | Phosphine sensitized photographic silver halide emulsions and elements |
GB31741/75A GB1507359A (en) | 1974-07-29 | 1975-07-29 | Photographic silver halide emulsions |
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Cited By (11)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS52101025A (en) * | 1976-02-20 | 1977-08-24 | Ricoh Co Ltd | Diazo copying material |
US4092171A (en) * | 1976-02-20 | 1978-05-30 | E. I. Du Pont De Nemours And Company | Organophosphine chelates of platinum and palladium as sensitizers |
US4346154A (en) * | 1981-06-22 | 1982-08-24 | Eastman Kodak Company | Antistain agent or antistain agent precursor in photographic silver halide element |
EP0562476A1 (en) | 1992-03-19 | 1993-09-29 | Fuji Photo Film Co., Ltd. | A silver halide photographic emulsion and a photographic light-sensitive material |
EP0563985A1 (en) | 1992-04-03 | 1993-10-06 | Fuji Photo Film Co., Ltd. | Silver halide color photographic material |
US5415992A (en) * | 1993-11-30 | 1995-05-16 | Eastman Kodak Company | Heat stabilized silver chloride photographic emulsions containing phosphine compounds |
EP0772079A2 (en) | 1995-10-31 | 1997-05-07 | Eastman Kodak Company | Light-sensitive silber halide emulsions and processes for their preparation |
EP0777153A1 (en) | 1995-11-30 | 1997-06-04 | Fuji Photo Film Co., Ltd. | Silver halide color photographic light-sensitive material |
EP1624337A2 (en) | 2004-08-02 | 2006-02-08 | Fuji Photo Film Co., Ltd. | Silver halide holographic sensitive material and system for taking holographic images by using the same |
EP1691237A2 (en) | 2005-02-15 | 2006-08-16 | Fuji Photo Film Co., Ltd. | Holographic recording material and holographic recording method |
EP1980908A1 (en) | 2007-04-13 | 2008-10-15 | FUJIFILM Corporation | Silver halide photographic material and image forming method using the same |
Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
SU195872A1 (en) * | 1966-07-08 | 1967-05-04 | METHOD FOR PRODUCING HALOGEN-SILVER FILM PHOTO MATERIALS | |
GB1295463A (en) * | 1969-03-12 | 1972-11-08 |
-
1974
- 1974-07-29 US US492956A patent/US3904415A/en not_active Expired - Lifetime
-
1975
- 1975-06-10 CA CA228,974A patent/CA1037761A/en not_active Expired
- 1975-07-29 GB GB31741/75A patent/GB1507359A/en not_active Expired
Patent Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
SU195872A1 (en) * | 1966-07-08 | 1967-05-04 | METHOD FOR PRODUCING HALOGEN-SILVER FILM PHOTO MATERIALS | |
GB1295463A (en) * | 1969-03-12 | 1972-11-08 |
Non-Patent Citations (1)
Title |
---|
Stauebe et al.: J. Am. Chem. Soc., Vol. 78, pages 976-977 (1956) * |
Cited By (11)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS52101025A (en) * | 1976-02-20 | 1977-08-24 | Ricoh Co Ltd | Diazo copying material |
US4092171A (en) * | 1976-02-20 | 1978-05-30 | E. I. Du Pont De Nemours And Company | Organophosphine chelates of platinum and palladium as sensitizers |
US4346154A (en) * | 1981-06-22 | 1982-08-24 | Eastman Kodak Company | Antistain agent or antistain agent precursor in photographic silver halide element |
EP0562476A1 (en) | 1992-03-19 | 1993-09-29 | Fuji Photo Film Co., Ltd. | A silver halide photographic emulsion and a photographic light-sensitive material |
EP0563985A1 (en) | 1992-04-03 | 1993-10-06 | Fuji Photo Film Co., Ltd. | Silver halide color photographic material |
US5415992A (en) * | 1993-11-30 | 1995-05-16 | Eastman Kodak Company | Heat stabilized silver chloride photographic emulsions containing phosphine compounds |
EP0772079A2 (en) | 1995-10-31 | 1997-05-07 | Eastman Kodak Company | Light-sensitive silber halide emulsions and processes for their preparation |
EP0777153A1 (en) | 1995-11-30 | 1997-06-04 | Fuji Photo Film Co., Ltd. | Silver halide color photographic light-sensitive material |
EP1624337A2 (en) | 2004-08-02 | 2006-02-08 | Fuji Photo Film Co., Ltd. | Silver halide holographic sensitive material and system for taking holographic images by using the same |
EP1691237A2 (en) | 2005-02-15 | 2006-08-16 | Fuji Photo Film Co., Ltd. | Holographic recording material and holographic recording method |
EP1980908A1 (en) | 2007-04-13 | 2008-10-15 | FUJIFILM Corporation | Silver halide photographic material and image forming method using the same |
Also Published As
Publication number | Publication date |
---|---|
CA1037761A (en) | 1978-09-05 |
GB1507359A (en) | 1978-04-12 |
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