US3737313A - Paper radiographic element containing silver halide grains rhodium salt sensitized,thioether ripened and polyvalent metal ion stabilized - Google Patents
Paper radiographic element containing silver halide grains rhodium salt sensitized,thioether ripened and polyvalent metal ion stabilized Download PDFInfo
- Publication number
- US3737313A US3737313A US00154164A US3737313DA US3737313A US 3737313 A US3737313 A US 3737313A US 00154164 A US00154164 A US 00154164A US 3737313D A US3737313D A US 3737313DA US 3737313 A US3737313 A US 3737313A
- Authority
- US
- United States
- Prior art keywords
- pat
- issued
- silver halide
- radiographic
- elements
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Lifetime
Links
- -1 silver halide Chemical class 0.000 title abstract description 72
- 229910052709 silver Inorganic materials 0.000 title abstract description 58
- 239000004332 silver Substances 0.000 title abstract description 58
- 150000003568 thioethers Chemical class 0.000 title abstract description 13
- 229910021645 metal ion Inorganic materials 0.000 title abstract description 11
- 150000003283 rhodium Chemical class 0.000 title description 7
- 238000000034 method Methods 0.000 abstract description 37
- 239000000084 colloidal system Substances 0.000 abstract description 22
- 238000000576 coating method Methods 0.000 abstract description 21
- 230000008569 process Effects 0.000 abstract description 18
- 239000003795 chemical substances by application Substances 0.000 abstract description 16
- 239000011248 coating agent Substances 0.000 abstract description 16
- BQCADISMDOOEFD-UHFFFAOYSA-N Silver Chemical compound [Ag] BQCADISMDOOEFD-UHFFFAOYSA-N 0.000 abstract description 12
- 238000009659 non-destructive testing Methods 0.000 abstract description 12
- 239000000839 emulsion Substances 0.000 description 49
- 230000005855 radiation Effects 0.000 description 19
- 150000003839 salts Chemical class 0.000 description 17
- 239000000975 dye Substances 0.000 description 16
- 239000000463 material Substances 0.000 description 16
- 108010010803 Gelatin Proteins 0.000 description 15
- 229920000159 gelatin Polymers 0.000 description 15
- 239000008273 gelatin Substances 0.000 description 15
- 235000019322 gelatine Nutrition 0.000 description 15
- 235000011852 gelatine desserts Nutrition 0.000 description 15
- 238000012545 processing Methods 0.000 description 12
- 239000000243 solution Substances 0.000 description 11
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 9
- 239000007864 aqueous solution Substances 0.000 description 9
- 150000001875 compounds Chemical class 0.000 description 9
- 229920000642 polymer Polymers 0.000 description 9
- 238000002601 radiography Methods 0.000 description 9
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 description 8
- 239000011230 binding agent Substances 0.000 description 8
- 229910052751 metal Inorganic materials 0.000 description 8
- 239000002184 metal Substances 0.000 description 8
- 238000012360 testing method Methods 0.000 description 8
- 229920001577 copolymer Polymers 0.000 description 7
- 239000000203 mixture Substances 0.000 description 7
- BASFCYQUMIYNBI-UHFFFAOYSA-N platinum Chemical compound [Pt] BASFCYQUMIYNBI-UHFFFAOYSA-N 0.000 description 6
- 230000035945 sensitivity Effects 0.000 description 6
- ZUNKMNLKJXRCDM-UHFFFAOYSA-N silver bromoiodide Chemical compound [Ag].IBr ZUNKMNLKJXRCDM-UHFFFAOYSA-N 0.000 description 6
- 238000012546 transfer Methods 0.000 description 6
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 5
- 239000011358 absorbing material Substances 0.000 description 5
- 125000000217 alkyl group Chemical group 0.000 description 5
- 239000000460 chlorine Substances 0.000 description 5
- PCHJSUWPFVWCPO-UHFFFAOYSA-N gold Chemical class [Au] PCHJSUWPFVWCPO-UHFFFAOYSA-N 0.000 description 5
- 229910052737 gold Inorganic materials 0.000 description 5
- 239000010931 gold Chemical class 0.000 description 5
- 229910001385 heavy metal Inorganic materials 0.000 description 5
- 230000001235 sensitizing effect Effects 0.000 description 5
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 5
- 239000002245 particle Substances 0.000 description 4
- 230000003595 spectral effect Effects 0.000 description 4
- 230000000087 stabilizing effect Effects 0.000 description 4
- 239000000126 substance Substances 0.000 description 4
- CNHDIAIOKMXOLK-UHFFFAOYSA-N toluquinol Chemical compound CC1=CC(O)=CC=C1O CNHDIAIOKMXOLK-UHFFFAOYSA-N 0.000 description 4
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 3
- 229910052693 Europium Inorganic materials 0.000 description 3
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 3
- 238000010521 absorption reaction Methods 0.000 description 3
- 238000005282 brightening Methods 0.000 description 3
- 229920002678 cellulose Polymers 0.000 description 3
- 230000007547 defect Effects 0.000 description 3
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- 125000000623 heterocyclic group Chemical group 0.000 description 3
- 238000004519 manufacturing process Methods 0.000 description 3
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 3
- 229910052697 platinum Inorganic materials 0.000 description 3
- 229920002401 polyacrylamide Polymers 0.000 description 3
- 239000004848 polyfunctional curative Substances 0.000 description 3
- NLKNQRATVPKPDG-UHFFFAOYSA-M potassium iodide Chemical compound [K+].[I-] NLKNQRATVPKPDG-UHFFFAOYSA-M 0.000 description 3
- 230000005070 ripening Effects 0.000 description 3
- 230000006641 stabilisation Effects 0.000 description 3
- 238000011105 stabilization Methods 0.000 description 3
- 229910052717 sulfur Inorganic materials 0.000 description 3
- 239000011593 sulfur Substances 0.000 description 3
- 239000002023 wood Substances 0.000 description 3
- 150000005206 1,2-dihydroxybenzenes Chemical class 0.000 description 2
- 150000005208 1,4-dihydroxybenzenes Chemical class 0.000 description 2
- DNJRKFKAFWSXSE-UHFFFAOYSA-N 1-chloro-2-ethenoxyethane Chemical compound ClCCOC=C DNJRKFKAFWSXSE-UHFFFAOYSA-N 0.000 description 2
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 2
- CDAWCLOXVUBKRW-UHFFFAOYSA-N 2-aminophenol Chemical class NC1=CC=CC=C1O CDAWCLOXVUBKRW-UHFFFAOYSA-N 0.000 description 2
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 description 2
- CIWBSHSKHKDKBQ-JLAZNSOCSA-N Ascorbic acid Chemical compound OC[C@H](O)[C@H]1OC(=O)C(O)=C1O CIWBSHSKHKDKBQ-JLAZNSOCSA-N 0.000 description 2
- CPELXLSAUQHCOX-UHFFFAOYSA-M Bromide Chemical compound [Br-] CPELXLSAUQHCOX-UHFFFAOYSA-M 0.000 description 2
- JIGUQPWFLRLWPJ-UHFFFAOYSA-N Ethyl acrylate Chemical compound CCOC(=O)C=C JIGUQPWFLRLWPJ-UHFFFAOYSA-N 0.000 description 2
- 206010073306 Exposure to radiation Diseases 0.000 description 2
- 229910052688 Gadolinium Inorganic materials 0.000 description 2
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 2
- QIGBRXMKCJKVMJ-UHFFFAOYSA-N Hydroquinone Chemical compound OC1=CC=C(O)C=C1 QIGBRXMKCJKVMJ-UHFFFAOYSA-N 0.000 description 2
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 2
- 150000000996 L-ascorbic acids Chemical class 0.000 description 2
- KDLHZDBZIXYQEI-UHFFFAOYSA-N Palladium Chemical compound [Pd] KDLHZDBZIXYQEI-UHFFFAOYSA-N 0.000 description 2
- 229910021607 Silver chloride Inorganic materials 0.000 description 2
- 229920002472 Starch Polymers 0.000 description 2
- 229910052771 Terbium Inorganic materials 0.000 description 2
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 2
- XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 description 2
- 239000002253 acid Substances 0.000 description 2
- 239000012190 activator Substances 0.000 description 2
- 150000001299 aldehydes Chemical class 0.000 description 2
- 125000005250 alkyl acrylate group Chemical group 0.000 description 2
- 125000002947 alkylene group Chemical group 0.000 description 2
- 229910052785 arsenic Inorganic materials 0.000 description 2
- RQNWIZPPADIBDY-UHFFFAOYSA-N arsenic atom Chemical class [As] RQNWIZPPADIBDY-UHFFFAOYSA-N 0.000 description 2
- 239000011324 bead Substances 0.000 description 2
- 150000001661 cadmium Chemical class 0.000 description 2
- KPWJBEFBFLRCLH-UHFFFAOYSA-L cadmium bromide Chemical compound Br[Cd]Br KPWJBEFBFLRCLH-UHFFFAOYSA-L 0.000 description 2
- YKYOUMDCQGMQQO-UHFFFAOYSA-L cadmium dichloride Chemical compound Cl[Cd]Cl YKYOUMDCQGMQQO-UHFFFAOYSA-L 0.000 description 2
- 125000004181 carboxyalkyl group Chemical group 0.000 description 2
- 239000001913 cellulose Substances 0.000 description 2
- ZYGHJZDHTFUPRJ-UHFFFAOYSA-N coumarin Chemical compound C1=CC=C2OC(=O)C=CC2=C1 ZYGHJZDHTFUPRJ-UHFFFAOYSA-N 0.000 description 2
- 230000003247 decreasing effect Effects 0.000 description 2
- 238000001514 detection method Methods 0.000 description 2
- 238000011161 development Methods 0.000 description 2
- 230000029087 digestion Effects 0.000 description 2
- 150000002081 enamines Chemical class 0.000 description 2
- 239000011888 foil Substances 0.000 description 2
- 150000004676 glycans Chemical class 0.000 description 2
- XMBWDFGMSWQBCA-UHFFFAOYSA-N hydrogen iodide Chemical compound I XMBWDFGMSWQBCA-UHFFFAOYSA-N 0.000 description 2
- NWVVVBRKAWDGAB-UHFFFAOYSA-N hydroquinone methyl ether Natural products COC1=CC=C(O)C=C1 NWVVVBRKAWDGAB-UHFFFAOYSA-N 0.000 description 2
- 125000002768 hydroxyalkyl group Chemical group 0.000 description 2
- 230000006872 improvement Effects 0.000 description 2
- 229910052741 iridium Inorganic materials 0.000 description 2
- GKOZUEZYRPOHIO-UHFFFAOYSA-N iridium atom Chemical compound [Ir] GKOZUEZYRPOHIO-UHFFFAOYSA-N 0.000 description 2
- 239000006224 matting agent Substances 0.000 description 2
- 150000002739 metals Chemical class 0.000 description 2
- 230000003287 optical effect Effects 0.000 description 2
- 239000003960 organic solvent Substances 0.000 description 2
- 150000002916 oxazoles Chemical class 0.000 description 2
- 230000035515 penetration Effects 0.000 description 2
- PNJWIWWMYCMZRO-UHFFFAOYSA-N pent‐4‐en‐2‐one Natural products CC(=O)CC=C PNJWIWWMYCMZRO-UHFFFAOYSA-N 0.000 description 2
- 150000004986 phenylenediamines Chemical class 0.000 description 2
- 229920001515 polyalkylene glycol Polymers 0.000 description 2
- 229920001282 polysaccharide Polymers 0.000 description 2
- 239000005017 polysaccharide Substances 0.000 description 2
- IOLCXVTUBQKXJR-UHFFFAOYSA-M potassium bromide Chemical compound [K+].[Br-] IOLCXVTUBQKXJR-UHFFFAOYSA-M 0.000 description 2
- 238000001556 precipitation Methods 0.000 description 2
- 230000001681 protective effect Effects 0.000 description 2
- NDGRWYRVNANFNB-UHFFFAOYSA-N pyrazolidin-3-one Chemical class O=C1CCNN1 NDGRWYRVNANFNB-UHFFFAOYSA-N 0.000 description 2
- 229910052761 rare earth metal Inorganic materials 0.000 description 2
- 229920005989 resin Polymers 0.000 description 2
- 239000011347 resin Substances 0.000 description 2
- MHOVAHRLVXNVSD-UHFFFAOYSA-N rhodium atom Chemical class [Rh] MHOVAHRLVXNVSD-UHFFFAOYSA-N 0.000 description 2
- 239000000377 silicon dioxide Substances 0.000 description 2
- ADZWSOLPGZMUMY-UHFFFAOYSA-M silver bromide Chemical compound [Ag]Br ADZWSOLPGZMUMY-UHFFFAOYSA-M 0.000 description 2
- HKZLPVFGJNLROG-UHFFFAOYSA-M silver monochloride Chemical compound [Cl-].[Ag+] HKZLPVFGJNLROG-UHFFFAOYSA-M 0.000 description 2
- SQGYOTSLMSWVJD-UHFFFAOYSA-N silver(1+) nitrate Chemical compound [Ag+].[O-]N(=O)=O SQGYOTSLMSWVJD-UHFFFAOYSA-N 0.000 description 2
- 239000011734 sodium Substances 0.000 description 2
- 229910052708 sodium Inorganic materials 0.000 description 2
- 239000002904 solvent Substances 0.000 description 2
- 239000008107 starch Substances 0.000 description 2
- 235000019698 starch Nutrition 0.000 description 2
- 125000004964 sulfoalkyl group Chemical group 0.000 description 2
- BDHFUVZGWQCTTF-UHFFFAOYSA-M sulfonate Chemical compound [O-]S(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-M 0.000 description 2
- 239000004094 surface-active agent Substances 0.000 description 2
- 229920002554 vinyl polymer Polymers 0.000 description 2
- ONDPHDOFVYQSGI-UHFFFAOYSA-N zinc nitrate Chemical compound [Zn+2].[O-][N+]([O-])=O.[O-][N+]([O-])=O ONDPHDOFVYQSGI-UHFFFAOYSA-N 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
- PSBDWGZCVUAZQS-UHFFFAOYSA-N (dimethylsulfonio)acetate Chemical group C[S+](C)CC([O-])=O PSBDWGZCVUAZQS-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
- VZYDKJOUEPFKMW-UHFFFAOYSA-N 2,3-dihydroxybenzenesulfonic acid Chemical class OC1=CC=CC(S(O)(=O)=O)=C1O VZYDKJOUEPFKMW-UHFFFAOYSA-N 0.000 description 1
- PDHFSBXFZGYBIP-UHFFFAOYSA-N 2-[2-(2-hydroxyethylsulfanyl)ethylsulfanyl]ethanol Chemical compound OCCSCCSCCO PDHFSBXFZGYBIP-UHFFFAOYSA-N 0.000 description 1
- JKFYKCYQEWQPTM-UHFFFAOYSA-N 2-azaniumyl-2-(4-fluorophenyl)acetate Chemical compound OC(=O)C(N)C1=CC=C(F)C=C1 JKFYKCYQEWQPTM-UHFFFAOYSA-N 0.000 description 1
- UGWULZWUXSCWPX-UHFFFAOYSA-N 2-sulfanylideneimidazolidin-4-one Chemical compound O=C1CNC(=S)N1 UGWULZWUXSCWPX-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
- WSGURAYTCUVDQL-UHFFFAOYSA-N 5-nitro-1h-indazole Chemical compound [O-][N+](=O)C1=CC=C2NN=CC2=C1 WSGURAYTCUVDQL-UHFFFAOYSA-N 0.000 description 1
- 241001479434 Agfa Species 0.000 description 1
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- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 1
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 1
- 229920002307 Dextran Polymers 0.000 description 1
- 229920002085 Dialdehyde starch Polymers 0.000 description 1
- RWSOTUBLDIXVET-UHFFFAOYSA-N Dihydrogen sulfide Chemical class S RWSOTUBLDIXVET-UHFFFAOYSA-N 0.000 description 1
- 239000004593 Epoxy Chemical class 0.000 description 1
- CTKINSOISVBQLD-UHFFFAOYSA-N Glycidol Chemical compound OCC1CO1 CTKINSOISVBQLD-UHFFFAOYSA-N 0.000 description 1
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- RVUMMKAOECEYND-UHFFFAOYSA-N [Na].Cc1cc(O)n2ncnc2n1 Chemical compound [Na].Cc1cc(O)n2ncnc2n1 RVUMMKAOECEYND-UHFFFAOYSA-N 0.000 description 1
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- 150000008055 alkyl aryl sulfonates Chemical class 0.000 description 1
- 229910052782 aluminium Inorganic materials 0.000 description 1
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- 150000004820 halides Chemical class 0.000 description 1
- 125000001188 haloalkyl group Chemical group 0.000 description 1
- 229910052736 halogen Inorganic materials 0.000 description 1
- 150000002366 halogen compounds Chemical class 0.000 description 1
- 150000002367 halogens Chemical group 0.000 description 1
- 150000002429 hydrazines Chemical class 0.000 description 1
- ZMZDMBWJUHKJPS-UHFFFAOYSA-N hydrogen thiocyanate Natural products SC#N ZMZDMBWJUHKJPS-UHFFFAOYSA-N 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-M hydroxide Chemical compound [OH-] XLYOFNOQVPJJNP-UHFFFAOYSA-M 0.000 description 1
- 125000004356 hydroxy functional group Chemical group O* 0.000 description 1
- 150000002443 hydroxylamines Chemical class 0.000 description 1
- 238000005213 imbibition Methods 0.000 description 1
- 150000002460 imidazoles Chemical class 0.000 description 1
- 229920000831 ionic polymer Polymers 0.000 description 1
- 150000002500 ions Chemical class 0.000 description 1
- 239000012948 isocyanate Substances 0.000 description 1
- 150000002513 isocyanates Chemical class 0.000 description 1
- 150000002576 ketones Chemical class 0.000 description 1
- 150000002602 lanthanoids Chemical group 0.000 description 1
- 229910052746 lanthanum Inorganic materials 0.000 description 1
- FZLIPJUXYLNCLC-UHFFFAOYSA-N lanthanum atom Chemical compound [La] FZLIPJUXYLNCLC-UHFFFAOYSA-N 0.000 description 1
- 230000002045 lasting effect Effects 0.000 description 1
- 239000004816 latex Substances 0.000 description 1
- 229920000126 latex Polymers 0.000 description 1
- 238000002386 leaching Methods 0.000 description 1
- 239000000314 lubricant Substances 0.000 description 1
- 238000004020 luminiscence type Methods 0.000 description 1
- CUONGYYJJVDODC-UHFFFAOYSA-N malononitrile Chemical compound N#CCC#N CUONGYYJJVDODC-UHFFFAOYSA-N 0.000 description 1
- 150000002696 manganese Chemical class 0.000 description 1
- 239000011159 matrix material Substances 0.000 description 1
- 238000010297 mechanical methods and process Methods 0.000 description 1
- 150000002730 mercury Chemical class 0.000 description 1
- 150000002731 mercury compounds Chemical class 0.000 description 1
- DZVCFNFOPIZQKX-LTHRDKTGSA-M merocyanine Chemical compound [Na+].O=C1N(CCCC)C(=O)N(CCCC)C(=O)C1=C\C=C\C=C/1N(CCCS([O-])(=O)=O)C2=CC=CC=C2O\1 DZVCFNFOPIZQKX-LTHRDKTGSA-M 0.000 description 1
- 150000002734 metacrylic acid derivatives Chemical class 0.000 description 1
- 125000001434 methanylylidene group Chemical group [H]C#[*] 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 150000002823 nitrates Chemical class 0.000 description 1
- 229910052762 osmium Inorganic materials 0.000 description 1
- SYQBFIAQOQZEGI-UHFFFAOYSA-N osmium atom Chemical compound [Os] SYQBFIAQOQZEGI-UHFFFAOYSA-N 0.000 description 1
- 150000002918 oxazolines Chemical class 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
- 230000000737 periodic effect Effects 0.000 description 1
- CMCWWLVWPDLCRM-UHFFFAOYSA-N phenidone Chemical compound N1C(=O)CCN1C1=CC=CC=C1 CMCWWLVWPDLCRM-UHFFFAOYSA-N 0.000 description 1
- NMHMNPHRMNGLLB-UHFFFAOYSA-N phloretic acid Chemical compound OC(=O)CCC1=CC=C(O)C=C1 NMHMNPHRMNGLLB-UHFFFAOYSA-N 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 239000004014 plasticizer Substances 0.000 description 1
- 229920003229 poly(methyl methacrylate) Polymers 0.000 description 1
- 229920002037 poly(vinyl butyral) polymer Polymers 0.000 description 1
- 239000004417 polycarbonate Substances 0.000 description 1
- 229920000515 polycarbonate Polymers 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 229920005596 polymer binder Polymers 0.000 description 1
- 239000002491 polymer binding agent Substances 0.000 description 1
- 239000004926 polymethyl methacrylate Substances 0.000 description 1
- 229920001155 polypropylene Polymers 0.000 description 1
- 229920003225 polyurethane elastomer Polymers 0.000 description 1
- 230000002035 prolonged effect Effects 0.000 description 1
- 108090000623 proteins and genes Proteins 0.000 description 1
- 102000004169 proteins and genes Human genes 0.000 description 1
- 150000003222 pyridines Chemical class 0.000 description 1
- 150000003236 pyrrolines Chemical class 0.000 description 1
- 125000001453 quaternary ammonium group Chemical group 0.000 description 1
- 239000001397 quillaja saponaria molina bark Substances 0.000 description 1
- 150000002910 rare earth metals Chemical class 0.000 description 1
- 238000012827 research and development Methods 0.000 description 1
- 229910052703 rhodium Inorganic materials 0.000 description 1
- 239000010948 rhodium Substances 0.000 description 1
- SONJTKJMTWTJCT-UHFFFAOYSA-K rhodium(iii) chloride Chemical compound [Cl-].[Cl-].[Cl-].[Rh+3] SONJTKJMTWTJCT-UHFFFAOYSA-K 0.000 description 1
- KZUNJOHGWZRPMI-UHFFFAOYSA-N samarium atom Chemical compound [Sm] KZUNJOHGWZRPMI-UHFFFAOYSA-N 0.000 description 1
- 229930182490 saponin Natural products 0.000 description 1
- 150000007949 saponins Chemical class 0.000 description 1
- 229910052711 selenium Inorganic materials 0.000 description 1
- 239000011669 selenium Substances 0.000 description 1
- 230000008313 sensitization Effects 0.000 description 1
- 235000012239 silicon dioxide Nutrition 0.000 description 1
- 229920002050 silicone resin Polymers 0.000 description 1
- 229940045105 silver iodide Drugs 0.000 description 1
- 229910001961 silver nitrate Inorganic materials 0.000 description 1
- 159000000000 sodium salts Chemical class 0.000 description 1
- GGCZERPQGJTIQP-UHFFFAOYSA-N sodium;9,10-dioxoanthracene-2-sulfonic acid Chemical compound [Na+].C1=CC=C2C(=O)C3=CC(S(=O)(=O)O)=CC=C3C(=O)C2=C1 GGCZERPQGJTIQP-UHFFFAOYSA-N 0.000 description 1
- UOULCEYHQNCFFH-UHFFFAOYSA-M sodium;hydroxymethanesulfonate Chemical compound [Na+].OCS([O-])(=O)=O UOULCEYHQNCFFH-UHFFFAOYSA-M 0.000 description 1
- 238000001228 spectrum Methods 0.000 description 1
- 238000003892 spreading Methods 0.000 description 1
- 230000007480 spreading Effects 0.000 description 1
- 239000003381 stabilizer Substances 0.000 description 1
- 229910001220 stainless steel Inorganic materials 0.000 description 1
- 239000010935 stainless steel Substances 0.000 description 1
- 150000001629 stilbenes Chemical class 0.000 description 1
- 235000021286 stilbenes Nutrition 0.000 description 1
- 125000005504 styryl group Chemical group 0.000 description 1
- 150000005846 sugar alcohols Polymers 0.000 description 1
- 150000003460 sulfonic acids Chemical class 0.000 description 1
- 229920001059 synthetic polymer Polymers 0.000 description 1
- 150000003498 tellurium compounds Chemical class 0.000 description 1
- 238000010998 test method Methods 0.000 description 1
- 150000003557 thiazoles Chemical class 0.000 description 1
- 150000003549 thiazolines Chemical class 0.000 description 1
- ANRHNWWPFJCPAZ-UHFFFAOYSA-M thionine Chemical compound [Cl-].C1=CC(N)=CC2=[S+]C3=CC(N)=CC=C3N=C21 ANRHNWWPFJCPAZ-UHFFFAOYSA-M 0.000 description 1
- UMGDCJDMYOKAJW-UHFFFAOYSA-N thiourea Chemical class NC(N)=S UMGDCJDMYOKAJW-UHFFFAOYSA-N 0.000 description 1
- 239000004408 titanium dioxide Substances 0.000 description 1
- 238000007738 vacuum evaporation Methods 0.000 description 1
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
- 230000000007 visual effect Effects 0.000 description 1
- 229920003176 water-insoluble polymer Polymers 0.000 description 1
- 229910052725 zinc Inorganic materials 0.000 description 1
- 239000011701 zinc Substances 0.000 description 1
- 239000011787 zinc oxide Substances 0.000 description 1
Classifications
-
- G—PHYSICS
- G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
- G03C—PHOTOSENSITIVE MATERIALS FOR PHOTOGRAPHIC PURPOSES; PHOTOGRAPHIC PROCESSES, e.g. CINE, X-RAY, COLOUR, STEREO-PHOTOGRAPHIC PROCESSES; AUXILIARY PROCESSES IN PHOTOGRAPHY
- G03C1/00—Photosensitive materials
- G03C1/005—Silver halide emulsions; Preparation thereof; Physical treatment thereof; Incorporation of additives therein
- G03C1/06—Silver halide emulsions; Preparation thereof; Physical treatment thereof; Incorporation of additives therein with non-macromolecular additives
- G03C1/42—Developers or their precursors
-
- G—PHYSICS
- G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
- G03C—PHOTOSENSITIVE MATERIALS FOR PHOTOGRAPHIC PURPOSES; PHOTOGRAPHIC PROCESSES, e.g. CINE, X-RAY, COLOUR, STEREO-PHOTOGRAPHIC PROCESSES; AUXILIARY PROCESSES IN PHOTOGRAPHY
- G03C1/00—Photosensitive materials
- G03C1/005—Silver halide emulsions; Preparation thereof; Physical treatment thereof; Incorporation of additives therein
- G03C1/06—Silver halide emulsions; Preparation thereof; Physical treatment thereof; Incorporation of additives therein with non-macromolecular additives
- G03C1/08—Sensitivity-increasing substances
- G03C1/09—Noble metals or mercury; Salts or compounds thereof; Sulfur, selenium or tellurium, or compounds thereof, e.g. for chemical sensitising
-
- 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
- G03C1/34—Fog-inhibitors; Stabilisers; Agents inhibiting latent image regression
-
- 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
- G03C5/00—Photographic processes or agents therefor; Regeneration of such processing agents
- G03C5/16—X-ray, infrared, or ultraviolet ray processes
Definitions
- This invention relates to radiographic image-recording elements and to processes employing such materials.
- this invention relates to radiographic elements comprising single-sided silver halide coatings and optionally containing luminescent intensifying screens.
- this invention relates to radiographic recording systems primarily designed for non-destructive testing and industrial use, which systems contain low silver content which unexpectedly provides improved characteristics to said systems.
- radiographic material has been selected primarily on the basis of balancing the opposing factors of high quality in the image recorded and short exposure time to the object being tested.
- a high quality film requires a slower, finer grained element and where a short exposure time is sought, a faster element would be required.
- this demand for high radiographic quality or short exposure time has found general acceptance by employing radiographic films usually coated on a cellulose acetate support and coated on each side with a radiation sensitive material, such as silver halide. With the increased cost of silver and the great need for more routine testing of mass produced items, cost becomes an important factor along with the faithful reproduction of the object tested.
- an image of lasting quality is an essential requirement so that good contrast and high photographic quality are important aspects in industrial radiographic elements.
- radiographic films having the qualities of good definition, high contrast, maximum density and moderate developing time.
- fine grain, high contrast films such as Kodak Industrial X-ray film Type M have been developed for use in direct exposure or with lead foil screens having a silver coverage on each side of their supports of about 900 milligrams/ft.
- the best type of industrial radiographic element is one which is thickly coated with a fine grain silver halide in order to give high contrast and reduce the general exposure time.
- radiographic element particularly suitable for nondestructive testing, which element is relatively inexpensive, highly sensitive to direct and screen type exposure and is capable of providing readily accessible images of high quality on site, that is, away from the laboratory darkroom.
- high contrast and fast emulsions can be utilized for radiographic applications.
- high speed projection emulsions such as thoseparticularly useful in photographic printing papers like enlarging papers, or designed for typesetting use, such as those disclosed in Sidebotham (US. 3,488,709) are unsuited for radiographic use because emulsion streaking and structure and quantum mottle, unobjectional for enlargements and noncontact application, are wholly intolerable for reproducing radiographic images in nondestructive testing.
- an improved photographic image-recording element which comprises a support bearing one sided thereof a radiation sensitive silver halide layer of low coating density dispersed in a hydrophilic colloid of a proportionately higher coating density.
- the element described herein is possessed of high speed, high contrast, and extraordinary physical characteristics which render it uniquely adaptable to industrial radiography and in particular the nondestructive testing of metal objects.
- the element sodescribed can contain an incorporated developer and likewise can comprise an integral or non-integral luminescent intensitfying screen to enhance the image forming process. This element provides unexpected improvements in the marked decrease in quantum mottle without impairing the intricately balanced system of'speed, image sharpness and contrast at the expense of prolonged exposure to radiation such as X-rays and gamma rays.
- a radiographic element comprising an incorporated developer layer, a radiation sensitive layer comprising (a) a thioether ripened silver halide emulsion precipitated in the presence of a rhodium salt and (b) a stabilizing amount of a polyvalent metal salt, i.e., divalent, trivalent or tetravalent metal salt, and a hydrophilic colloid containing overcoat layer.
- a polyvalent metal salt i.e., divalent, trivalent or tetravalent metal salt
- the rhodium salts useful in this invention can be any suitable rhodium salt including ammonium chlororhodate, rhodium chloride, and the like.
- still other salts such as K IrCl Bi(NO -5H O; H PtCl K IrCl and K O Cl are effective as are other salts of arsenic, gold, antimony and various mixtures thereof.
- the polyvalent metals such as those di-, tri-, and tetravalent metals and their salts which enhance the sensitivity and speed of the silver halide grains include trivalent antimony, bismuth, arsenic, gold, iridium, rhodium and the like.
- Tetravalent metal ions include platinum, osmium, iridium and the like.
- Divalent metal ions include cadmium such as cadmium chloride, cadmium nitrate, and zinc, like zinc nitrate and various manganese salts and the like
- the element so-described comprises a support bearing a radiaiton sensitive layer containing silver halide grains dispersed in a hydrophilic colloid and precipitated in the presence of a rhodium salt, and added to said already formed grains, a stabilizing concentration of a salt of a poly-valent i.e. a di-, trior tetra valent metal ion, the improvement comprising employing a coating concentration of from about 350 to about 450 ing/ft. of said hydrophilic colloid and from 100 to about 200 mg./ft.
- a photographic element and particularly a radiographic element, i.e. one which is radiation sensitive comprising a support bearing a layer comprising a hy r philic colloid in a. concentration from about 350 to about 450 rug/ft. in which is dispersed a concentration of silver in a coverage i.e. a coating density of less than about 200 mg./ft. but in a concentration suflicient to provide radiation sensitivity.
- This improved radiographic element of high image quality comprises a support bearing a high speed, high contrast low silver halide containing layer, said silver halide dispersed in a hydrophilic colloid coated at a density of about 350 to about 450 mg./ft.
- high contrast is meant that value equal to the difference between the densities of two areas of the sensitive layer after exposure and processing.
- the contrast is about 4 to about 9 and preferably about 4.5 to about 5.5.
- the above described radiographic element provides a high speed, high contrast image in a short time by incorporating in the above described element suitable developing agents.
- a process for obtaining a high quality radiographic image of a test subject which comprises exposing to a radiation source, said subject in proximate contact, i.e. indirect contact or in close relation therewith, a radiographic element comprising a support hearing a layer comprising a hydrophilic colloid laid down in a coating concentration of from about 350 to about 450 mg./ft. in which is dispersed a radiation sensitive amount of silver halide in a coverage of less than about 200 mg./ ft. and preferably from about mg./ft. to about mg./ft.
- a coarse or large size radiation sensitive silver halide grain such as a silver bromoiodide grain, in order to provide a fast, light sensitive element so that the exposure to radiation is minimized to the patient. From this, one can readily see that the light or energy absorption requirements of that type of radiation-sensitive element is lower, than the type of element customarily used heretofore for industrial radiography. In particular, the industrial radiograph used of element customarily used heretofore for industrial radiography.
- the industrial radiograph used heretofore comprises a fine grain silver halide emulsion or layer containing said fine grains and, in view of the requirement for absorbing as much X-ray or gamma-ray as possible, the element necessarily contains a very high coating density of silver in order to absorb said radiation.
- the present invention becomes all the more unobvious in that it uses (a) a radiation-sensitive element having coarse silver halide grains typically used for medical radiography and (b) employs said coarse grain in a very light coating density quite unlike heretofore uses elements and processes for industrial radiographs.
- Mottle is actually believed to be the combination of various components observed in radiographic elements.
- quantum mottle the major contributing factor, results from statistical fluctuations in the spatial distribution of the number of photons in the X-ray image while structure mottle results from irregularities in the screen structure.
- the combination of both of these unwanted defects is called screen mottle and they are particularly apparent whenever a fast-image forming system is used and also as the radiation energy is increased, such as in the high exposure time required in industrial radiography.
- radiation it will be understood to mean the transmission of energy through space such as the diffusion of or transfer of energy through matter.
- it relates to the stream of X-rays, gamma-rays and the like of (1) relatively short Wave lengths, such as 0.062 A. and (2) hard X-rays of shorter wave lengths of higher penetration, i.e. 0.19-0.43 A. and (3) soft X-rays of low penetration having a wave length of from about 11.9 to about 13.6 A.
- the silver halide layers and emulsions used with this invention can comprise silver chloride, silver bromide, silver bromoiodide, silver chlorobromoiodide or mixtures thereof.
- the emulsions are generally coarse grain, i.e., having a grain size of 0.54.0 1 and can be prepared by any of the well-known procedures, e.g. single jet emulsions, double jet emulsions, such as Lippman emulsions, ammoniacal emulsions, thiocyanate or thioether ripened emulsions such as those described in Nietz et al. U.S. Pat. 2,222,264 issued Nov. 19, 1940; Illingsworth U.S. Pat.
- the silver halide is preferably unfogged and contains at least about 50% bromide, less than about 10% iodide and less than about 50% chloride on a molar basis.
- the silver halide is a silver bromoiodide containing about 95% to about 99% bromide, i.e., about 5% to about 1% iodide.
- Surface image emulsions can be used or internal image emulsions such as those described in Davey et al. U.S. Pat. 2,592,250 issued May 8, 1952; Porter et al. U.S. Pat. 3,206,313 issued Sept.
- Negative type emulsions can be used or direct positive emulsions such as those described in Leerrnakers US. Pat. 2,184,013 issued Dec. 19, 1939; Kendall et al. U.S. Pat. 2,541,472 issued Feb. 13, 1951; Berriman U.S. Pat. 3,367,778 issued Feb. 6, 1968; Schouwenaars British Pat. 723,019 issued Feb. 2, 1955; Illingsworth et al. French Pat. 1,520,821 issued Mar. 4, 1968; Ives U.S. Pat.
- the emulsions can be regular grain emulsions such as the type described in Klein and Moisar, J. Phot. Sci., vol. 12, No. 5, September/October 1964, pp. 242251.
- the silver halide layers and emulsions used with this invention can be unwashed or washed to remove soluble salts.
- the soluble salts are removed by chill-setting and leaching or the emulsion can be coagulation washed, e.g. by the procedures described in Hewitson et al. U.S. Pat. 2,618,556 issued Nov. 18, 1952; Yutzy et al. U.S. Pat. 2,614,928 issued Oct. 21, 1952; Yackel U.S. Pat. 2,565,418 issued Aug. 21, 1951; Hart et al. U.S. Pat. 3,241,969 issued Mar. 22, 1966; and Waller et al. U.S. Pat. 2,489,341 issued Nov. 29, 1949.
- the silver halide layers and emulsions used with this invention can be sensitized with chemical sensitizers, such as with reducing agents; sulfur, selenium or tellurium compounds; gold, platinum or palladium compounds; or combinations of these.
- chemical sensitizers such as with reducing agents; sulfur, selenium or tellurium compounds; gold, platinum or palladium compounds; or combinations of these.
- Suitable procedures are described 6 in Sheppard et al. U.S. Pat. 1,623,499 issued Apr. 5, 1927; Waller et al. U.S. Pat. 2,399,083 issued Apr. 23, 1946; McVeigh U.S. Pat. 3,297,447 issued Jan. 10, 1967; and Dunn U.S. Pat. 3,297,446 issued Jan. 10, 1967.
- This silver halide layers and emulsions used with this invention can contain speed increasing compounds such as polyalkylene glycols, cationic surface active agents and thioethers or combinations of these as described in Piper U.S. Pat. 2,886,437 issued May 12, 1959; Damn et al. U.S. Patent 3,046,134 issued July 24, 1962; Carrol et al. U.S. Pat. 2,944,900 issued July 12, 1960; and Golfe U.S. Pat. 3,294,540 issued Dec. 27, 1966.
- speed increasing compounds such as polyalkylene glycols, cationic surface active agents and thioethers or combinations of these as described in Piper U.S. Pat. 2,886,437 issued May 12, 1959; Damn et al. U.S. Patent 3,046,134 issued July 24, 1962; Carrol et al. U.S. Pat. 2,944,900 issued July 12, 1960; and Golfe U.S. Pat. 3,294,540 issued Dec. 27, 1966.
- the silver halide layers and emulsions used in the practice of this invention can be protected against the production of fog and can be stabilized against loss of sensitivity during keeping.
- Suitable antifoggants and stabilizers each used alone or in combination include thiazolium salts described in Brooker et al. U.S. Pat. 2,131,038 issued Sept. 27, 1938, and Allen et al. U.S. Pat. 2,694,716 issued Nov. 16, 1954; the azaindenes described in Piper U.S. Pat. 2,886,437 issued May 12, 1959; and Heimbach et al. U.S. Pat. 2,444,605 issued July 6, 1948; the mercury salts as described in Allen et al. U.S. 2,728,663 issued Dec.
- the radiographic elements of this invention can contain an incorporated developer comprising one or more developing agents such as hydroquinones, catechols, aminophenols, 3-pyrazolidones, ascorbic acid and its derivatives, reductones and phenylenediamines. Combinations of developing agents can be employed in the practice of the invention.
- the developing agents can be in a silver halide emulsion and/ or in an other suitable location in the photographic element.
- the developing agents can be added from suitable solvents or in the form of dispersions as described. in Yackel U.S. Pat. 2,592,368 issued Apr. 8, 1952 and Dunn et al., French Pat. 1,505,778.
- the radiographic and other hardenable layers used in the practice of this invention can be hardened by various organic or inorganic hardeners, alone or in combination, such as the aldehydes, and blocked aldehydes, ketones, carboxylic and carbonic acid derivatives, sulfo nate esters sulfonyl halides and vinyl sulfonyl ethers, active halogen compounds, epoxy compounds, aziridines, active olefines, isocyanates, carbodiirnides, mixed function hardeners and polymeric hardeners such as oxidized polysaccharides like dialdehyde starch and oxyguar gum and the like.
- various organic or inorganic hardeners such as the aldehydes, and blocked aldehydes, ketones, carboxylic and carbonic acid derivatives, sulfo nate esters sulfonyl halides and vinyl sulfonyl ethers, active halogen compounds, epoxy compounds,
- radiographic emulsions and elements described in the practice of this invention can contain various colloids alone or in combination as vehicles, binding agents and various layers.
- Suitable hydrophilic materials include both naturally-occurring substances such as proteins, for example, gelatin, gelatin derivatives, cellulose derivatives, polysaccharides such as dextran, gum arabic and the like; and synthetic polymeric substances such as water soluble polyvinyl compounds like poly(vinylpyrrolidone), acrylamide polymers and the like.
- radiographic emulsion layers and other layers of a photographic element employed in the practice of this invention can also contain alone or in combination with hydrophilic water permeable colloids, other synthet is polymeric compounds such as dispersed vinyl compounds such as in latex form and particularly those which increase the dimensional stability of the photographic materials.
- Suitable synthetic polymers include those described, for example, in Nottorf U.S. Pat. 3,142,568 issued July 28, 1964; White U.S. Pat. 3,193,386 issued July 6, 1965; Houck et a1. U.S. Pat. 3,062,674 issued Nov. 6, 1962; Houck et al. U.S. Pat. 3,220,844 issued Nov. 30, 1965; Ream et al. U.S. Pat.
- the radiographic elements used with this invention can contain antistatic or conducting layers, such layers can comprise soluble salts, e.g. chlorides, nitrates, etc., evaporated metal layers, ionic polymers such as those described in Minsk U.S. Pat. 2,861,056 issued Nov. 18, 1958 and Sterman et al., U.S. Patent 3,206,312 issued Sept. 14, 1965 or insoluble inorganic salts such as those described in Trevoy U.S. Pat. 3,428,451 issued Feb. 18, 1969.
- soluble salts e.g. chlorides, nitrates, etc.
- evaporated metal layers ionic polymers
- U.S. Patent 3,206,312 issued Sept. 14, 1965
- insoluble inorganic salts such as those described in Trevoy U.S. Pat. 3,428,451 issued Feb. 18, 1969.
- the radiographic layers employed in the practice of this invention can contain plasticizers and lubricants such as polyalcohols, e.g. glycerin and diols of the type described in Milton et al., U.S. Patent 2,960,404 issued Nov. 1, 1966; fatty acids or esters such as those described in Robijns U.S. Pat. 2,588,765 issued Apr. 11, 1952, and Duane U.S. Pat. 3,121,060 issued Feb. 11, 1964; and silicone resins such as those described in Du Pont British Patent 955,061 issued Apr. 15, 1964.
- plasticizers and lubricants such as polyalcohols, e.g. glycerin and diols of the type described in Milton et al., U.S. Patent 2,960,404 issued Nov. 1, 1966; fatty acids or esters such as those described in Robijns U.S. Pat. 2,588,765 issued Apr. 11, 1952, and Duane U.S. Pat. 3,121,060 issued
- the radiographic layers employed in the practice of this invention can contain surfactants such as saponin; anionic compounds such as the alkyl aryl sulfonates described in Baldsiefen U.S. Pat. 2,600,831 issued June 17, 1952; amphoteric compounds such as those described in Ben-Ezra U.S. Pat. 3,133,816 issued May 19, 1964; and water soluble adducts of glycidol and an alkyl phenol such as those described in Olin Mathieson British Pat. 1,022,878 issued Mar. 16, 1966.
- surfactants such as saponin
- anionic compounds such as the alkyl aryl sulfonates described in Baldsiefen U.S. Pat. 2,600,831 issued June 17, 1952
- amphoteric compounds such as those described in Ben-Ezra U.S. Pat. 3,133,816 issued May 19, 1964
- water soluble adducts of glycidol and an alkyl phenol such as those
- radiographic elements employed in the practice of this invention can contain matting agents such as starch, titanium dioxide, zinc oxide, silica, polymeric beads including beads of the type described in Jelley et al., U.S. 'Pat. 2,992,101 issued July 11, 1961 and Lynn U.S. Pat. 2,701,245, issued Feb. 1, 1955.
- matting agents such as starch, titanium dioxide, zinc oxide, silica, polymeric beads including beads of the type described in Jelley et al., U.S. 'Pat. 2,992,101 issued July 11, 1961 and Lynn U.S. Pat. 2,701,245, issued Feb. 1, 1955.
- the radiographic elements used in this invention can contain brightening agents including stilbenes, tniazines, oxazoles and coumarin brightening agents.
- Brightening agents including stilbenes, tniazines, oxazoles and coumarin brightening agents.
- Water soluble brightening agents can be used such as those described in Alberz et al., German Pat. 972,067 and McFall et al., U.S. Pat. 2,933,390 issued Apr. 19, 1960 or dispersions of brighteners may be used such as those described in Jansen German Pat. 1,150,274, Oetiker et al., U.S. Pat. 3,406,070 issued Oct. 15, 1968 and Heidke French Pat. 1,530,244.
- Spectral sensitizing dyes can be used conveniently to confer additional sensitivity to the radiation sensitive silver halide emulsion of the radiographic elements of the invention.
- additional spectral sensitization can be obtained by treating the emulsion with a solution of a sensitizing dye in an organic solvent or the dye can be 'added in the form of a dispersion as described in Owens et al. British Pat. 1,154,781 issued June 11, 1969.
- the dye is either added to the emulsion as a final step or at some earlier stage.
- Spectral sensitizers which can be used include the cyanines, merocyanines, complex (tri or tetranuclear) merocyanines, complex (tri or tetranuclear) cyanines, holopolar cyanines, styryls, hemicyanines (e.g. enamine hemicyanines), oxonols and hemioxonols.
- Dyes of the cyanine classes can contain such basic nuclei as the thiazolines, oxazolines, pyrrolines, pyridines, oxazoles, thiazoles, selenazoles and imidazoles.
- Such nuclei can contain alkyl, 'alkylene, hydroxyalkyl, sulfoalkyl, carboxyalkyl, aminoalkyl and enamine groups and can be fused to carbocyclic or heterocyclic ring systems either unsubstituted or substituted with halogen, phenyl, alkyl, haloalkyl, cyano, or alkoxy groups.
- the dyes can be symmetrical or unsymmetrical and can contain alkyl, phenyl, enamine or heterocyclic substitutents on the methine or polymethine chain.
- the merocyanine dyes can contain the basic nuclei mentioned above as Well as acid nuclei such as thiohydantoins,
- .rhodanines oxazolidenediones, thiazolidenediones, barbituric acids, thiazolineones, and malononitrile.
- These acid nuclei can be substituted with alkyl, alkylene, phenyl, carboxyalkyl, sulfoalkyl, hydroxyalkyl, alkoxyalkyl, alkylamino groups, or heterocyclic nuclei. Combinations of these days can be used, if desired.
- supersensitizing addenda which do not absorb visible light
- addenda which do not absorb visible light
- ascorbic acid derivatives for instance, ascorbic acid derivatives, azaindenes, cadmium salts, and organic sulfonic acids as described in McFall et al., U.S. Pat. 2,933,390 issued Apr. 19, 1960, and Jones et al. U.S. Pat. 2,937,089 issued May 17, 1960.
- the various layers, including the radiographic layers, employed in the practice of this invention can contain light absorbing materials and filter dyes such as those described in Sawdey U.S. Pat. 3,253,921 issued May 31, 1966; Gaspar U.S. Pat. 2,274,782 issued Mar. 3, 1942; Silberstein et al. U.S. Pat. 2,527,583 issued Oct. 31, 1950, and VanCampen U.S. Pat. 2,956,879 issued Oct. 18, 1960.
- the dyes can be mordanted, for example, as described in Milten et al., U.S. Pat. 3,282,699 issued Nov. 1, 1966.
- the sensitizing dyes and other addenda used in the practice of this invention can be added from water solutions or suitable organic solvent solutions can be used.
- the compounds can be added using various procedures including those described in Collins et al., U.S. Pat. 2,912,343 issued Nov. 10, 1959; McCrossen et al., U.S. Pat. 3,342,605 issued Sept. 19, 1967; Audran U.S. Pat. 2,996,287 issued Aug. 15, 1961 and Johnson et al., U.S. Pat. 3,425,835 issued Feb. 4, 1969.
- radiographic layers used in the practice of this invention can be coated by various coating procedures including dip coating, air knife coating, curtain coating, or extrusion coating using hoppers of the type described in Beguin U.S. Pat. 2,681,294 issued June 15, 1954. If desired, two or more layers may be coated simultaneously by the procedures described in Russell U.S. Pat. 2,761,791 issued Sept. 4, 1956 and Wynn British Pat. 837,095.
- This invention also can be used for silver halide layers coated by vacuum evaporation as described in British Pat. 968,- 453 and LuValle et al., U.S. Pat. 3,219,451 issued Nov. 23, 1965. a
- This invention can be used with elements designed for color photography, for example, elements containing color-forming couplers such as those described in Frohlich et al., U.S. Pat. 2,376,679 issued May 22, 1945; Jelley et al., U.S. Pat. 2,322,027 issued June 15, 1943; Fierke et al., U.S. Pat. 2,801,171 issued July 30, 1957; Godowsky U.S. Pat. 2,698,794 issued Jan. 4, 1955; Barr et al., U.S. Pat. 3,227,554 issued Jan. 4, 1966; and Graham et al., U.S. Pat.
- Radiographic elements prepared according to this invention can be processed by various methods including processing in alkaline solutions containing conventional developing agents such as hydroquinones, catechols, aminophenols, 3-pyrazolidones, phenylenediamines, ascorbic acid derivatives, hydroxylamines, hydrazines, reductones and the like; web processing such as described in Tregillus et al. U.S. Pat. 3,179,517 issued Apr. 20, 1965; stabilization processing as described in Russell et al. Stabilization Processing of Films and Papers, PSA Journal, vol. 163, August 1950; monobath processing as described in Levy Combined Development and Fixation of Photographic Images with Monobaths, Phot. Sci. and Eng., vol. 2, No.
- conventional developing agents such as hydroquinones, catechols, aminophenols, 3-pyrazolidones, phenylenediamines, ascorbic acid derivatives, hydroxylamines, hydrazines, reductones and the like
- web processing such as
- the photographic elements of this invention can be processed in hardening developers such as those described in Allen et al. U.S. Pat. 3,232,761 issued Feb. 1, 1966; in roller transport processors such as those described in Russell et al. U.S. Pat. 3,025,779 issued Mar. 20, 1962; or by surface application processing as described in Example 3 of Kitze U.S. Pat. 3,418,132 issued Dec. 24, 1968.
- This invention can be used with elements designed for colloid transfer processes such as described in Yutzy et al., U.S. Pat. 2,716,059 issued Aug. 23, 1953; silver salt ditfusion transfer processes such as described in Rott U.S. Pat. 2,352,014 issued June 20, 1944; Land U.S. Pat. 2,543,181 issued Feb. 27, 1951; Yackel et al. U.S. Pat. 3,020,155 issued Feb. 6, 1962; and Land U.S. Pat. 2,861,- 885 issued Nov. 25, 1958; color image transfer processes such as described in Rogers U.S. Pats. 3,087,817 issued Apr.
- This invention may be used in elements designed for recording print out images as described in Fallesen U.S. Pat. 2,369,449 issued Feb. 13, 1945 or Bacon et al. U.S. Pat. 3,447,927 issued June 3, 1969; elements designed for processing by heat as described in Sorensen et al. U.S. Pat. 3,152,904 issued Oct. 13, 1964; Morgan et al. U.S. Pat. 3,457,075 issued July 22, 1969; Stewart et al. U.S. Pat. 3,312,550 issued Apr. 4, 1967 and Colt U.S. Pat. 3,418,122 issued Dec. 24, 1968.
- This invention can be used in elements designed for physical development such as those described in Agfa British Pat. 920,277 and Gilrnan et al. British Pat. 1,131,238.
- Hydrophilic colloid materials which can be used in the practice of the invention include various waterpermeable binder vehicles which materials can be suspended in colloidal dispersions.
- Hydrophilic colloids suitable as binder vehicles and layers include proteinaceous compounds such as, for example, gelatin, colloidal albumin and other hydrophilic colloids such as, for example, polyvinyl compounds, cellulose derivatives, acrylamide polymers, etc., though gelatin materials are preferred.
- the high molecular weight materials for binder vehicles and layers which are generally consider soluble in aqueous solutions and do not form small discrete particles when mixed with an aqueous gelatin emulsion, as can be determined upon observation of a photomicrograph, can be considered hydrophilic colloids for purposes of this invention.
- the phosphors in the X-ray intensifying screens possess the characteristic of having a substantial part, that is, more than half, of their total spectral emission at less than about 410 nm. This emission is substantially in the ultraviolet range of the spectrum and it has been found that a host matrix comprising at least one of certain heavy metal phosphors are particularly useful therefor. Such phosphors have a physical density greater than at least about 3.5 and preferably greater than 3.9.
- heavy metal phosphors including those made from the lanthanide group of the periodic table.
- the latter rare earth elements have an atomic number in the range of between 58 to 71 and include lanthanum, cerium, Samarium, gadolinium and the like.
- Particularly eifective heavy metal phosphors are those such as lanthanideor leadactivated BaSO and BaSrSO such as europium activated BaSrSO lead-activated barium silicates, gadolinium-activated yttrium oxide, and barium fluoride, barium fluoride chloride and the like. Said phosphors can be further activated by rare earth activators alone and in combination. These phosphors can be prepared by a number of ways, such as set forth in Belgian Pat. 703,998 issued Mar. 18, 1969 to Luckey; in Buchanan et al. J. Applied Physics, vol. 39, pp.
- a preferred use of the radiographic elements necessary to the invention herein is in combination with radiographic intensifying screens particularly because the absorption of X-rays by the phosphor host is so high.
- the absorption of X-ray energy by the radiographic screens comprising certain phosphors is so high that single sided radiographic systems can be employed which systems form part of the present invention.
- These single-sided radiographic systems provide such extraordinary sharpness and high speed that they are equal or superior to similar results obtained by conventional double-sided systems.
- the various phosphors exhibiting the desirable luminescence is the terbium-activated lanthanum oxysulfide which has a negligible after-glow and whose green emission makes it particularly suitable for fluoroscopic and radiographic application.
- the intensifying fluorescent screens which can form part of the radiographic element of our invention, consist essentially of phosphors which can be dispersed or suspended in a suitable binder such as those set forth in U.S. Pats. 3,300,310 and 3,300,311 supra. which employ a water-soluble copolymer of alkylacrylate and acrylic acid, copolymers of vinyl chloride and vinyl acrylate, polyvinyl butyral as set forth in German Pat. 1,186,332 issued I an.
- a coherent film-forming macromolecular polymer binder such as resins, polymers or copolymers of polycarbonate which comprise recurring carbonate units in the polymer chain, and the like, polymers of acrylic acid esters containing small percentages of a chlorine-containing derivative, such as acrylonitrile copolymers such as Hycar (a trademark of BF. Goodrich Chemical Company for the thus-described dry rubber polymers).
- binders include those screenbinders including blends of copolymers of ethyl acrylate, chloro ethyl vinyl ether with a poly alkyl methacrylate and polyurethane elastomers.
- the phosphors can be present in the binder in a wide variety of ratios such as, for example, from about 30:1 to about 4:1 and preferably in the range of about 16:1 to about 6:1.
- the coverage of the phosphor can vary over a wide range. Effective coverage can be determined through experimentation.
- a preferred coverage of said phosphor in the screen is in a range from about 15 to about 150 grams/ftF. With respect to general purpose screens good results are achieved with a coverage in the range of about 50 to grams/ft. and with respect to high definition screens a coverage of from about 15 to 35 grams/ft? yields good results.
- these screens can be coated in a variety of ways such as directly over the photographic layer or on both sides of a double coated or single coated element.
- Intermediate 1 l layers such as stripping layers, protective or overcoat layers, can likewise be employed between or over the X-ray emulsion layer and the intensifying screen.
- Said layers can comprise hydrophilic colloid material such as gelatin, gelatin derivatives, cellulose esters, alkyl acrylatecontaining polymers and the like.
- the radiographic elements of our invention employ, in addition to the phosphor-containing intensifying screen, a suitably supported image recording layer such as one comprising silver halide as disclosed hereinbefore.
- a suitably supported image recording layer such as one comprising silver halide as disclosed hereinbefore.
- the radiographic elements and combinations so described can be constructed such that the photographic elements are either separate, i.e. non-integral or integral, i.e. as a separate distinct layer of an element comprising a silver halide emulsion coated onto a support with the intensifying screen.
- Said silver halide can be present in a layer or coating such as a single coating on one side of a support.
- Suitable supports are those having the properties to permit their ready passage through a rapid automatic processor if desired.
- Said support should, therefore, be reasonably flexible and preferably able to maintain the dimensional stability and integrity of the various coatings thereon.
- Typical supports are fibrous materials used as supports such as cards or paper which are coated with ocolefin polymers, particularly polymers of a-olefins containing two to ten carbon atoms, as exemplified by polyethylene, polypropylene, ethylene-butene copolymers, and the like, give good results.
- said supports can comprise light absorbing materials either within the support itself, on a layer over and/or under said support, or both.
- the thickness of said support can vary as is well-known in the art in order to practice effectively our invention.
- the silver halide can comprise varying amounts of silver chloride, silver iodide, silver bromide, silver chlorobromide, silver brornoiodide and the like. Particularly good results are obtained with gelatino silver bromoiodide emulsions in which the average grain size of the silver brornoiodide crystals is in the range of about 0.5 to about 5 microns. These layers are applied by means well-known in the art.
- the photographic silver halide coatings can also contain additional additives, particularly those known to be beneficial in photographic emulsions.
- they can contain speed-increasing compounds, for example, onium salts, such as quaternary ammonium or ternary sulfonium salts, polyalkylene glycols, thioethers and the like.
- the photographic silver halide coatings can be stabilized with mercury compounds, azaindenes, quaternary benzothiazolium compounds, hydroxy substituted aromatic compounds, and the like.
- the photographic silver halide elements which are part of the radiographic combinations described herein provide very good results in image sharpness without absolute need for any dyes or other light absorbing materials. While there is no need for employing dyes or other light absorbing materials in either the film, the screen, or both, extraordinary results can be obtained by using such dyes and light absorbing materials.
- light absorbing dyes and materials can be in the emulsion layer or in an auxiliary layer such as a layer coated between the support and the emulsion layer, or the light absorbing dyes and materials can be included in both the emulsion and the auxiliary layer.
- These elements can also contain inert particles such as those often employed as matting agents in photographic elements. Suitable materials of this type include, for example, particles of silicon dioxide, glass, starch, polymethyl methacrylate and the like. Such inert particles are often included in an emulsion layer alone and in combination.
- These elements can likewise contain various protective overcoats such as those which comprise colloidal silica in an overcoat comprising gelatin and at least another hydrophilic colloid, including gelatin-compatible acrylic.
- Processing can be elfected'not only by utilizing the incorporated developer system but also in a variety of other ways including the multi-tank manual methods but preferably in a unidirectional, multi-roller high speed processing apparatus described in Belgian Patent 700,301 issued Aug. 31, 1967, to Barnes et a1. These processes can be eifected and the combinations of this invention can be processed respectively according to US. Patent 3,232,761 issued Feb. 1, 1966, to Allen and Burness, Reissue 26,601. Y
- the silver-containing film-screen combinations of our invention can likewise be used with unexpectedly good radiographic results in solvent transfer systems such as where single and double coatings are employed. In addition where positive images are so obtained they are easily converted to negative microfilm images either during or after processing. Equally good results are obtained when these novel combinations contain color couplers, such as those described in British Patent 799,588 issued Aug. 13, 1958, to Whitmore and Elins, and by using these novel combinations and processes in color film-containing systems. 3
- radiographic combinations are used effectively in recording X-ray images, and there is unexpectedly provided screen-film combinations having improved sharpness, and with vastly increased speed.
- EXAMPLE 1 A typical coarse-grained, silver brornoiodide (99:1) emulsion suitable for use in X-ray film elements is prepared by employing the double-jet" technique. An aqueous solution of potassium bromide and potassium iodide and another aqueous solution of silver nitrate are added simultaneously over a period of 10 minutes to an aqueous gelatin solution at 65.6 C. A thioether ripening agent, 1,8-dihydroxy-3,6-dithiooctane (10.9 g./mole Ag) is added to the precipitated emulsion which is then digested for approximately 30 minutes, salt 'coagulated, washed thoroughly, redispersed and sulfur and gold sensitized. The chemically sensitized emulsion is combined with the following solutions:
- the bottom layer is coated on paper support at 6.90 g. solution/ft therefore resulting in an incorporated developer layer containing approximately 222 mg. gelatin/ ft. 76 mg. methyl hydroquinone/ft. and 15 mg. 1- phenyl-3-pyrazolidone/ft.
- the radiographic element is then overcoated with a gelatin containing composition at 5.85 g. solution/fe thereby resulting in a layer containing approximately 53 mg. gelatin/ft?
- the dried multilayer radiographic element is exposed to X-ray radiation (110 kv., 10 ma.) for 15 seconds at a distance of 3 feet and then processed by passing the exposed element through an Eastman Kodak Ektamatic Processor which activates the incorporated developer element and stabilize it.
- the processed element is assigned a relative speed of 100 and is equal in speed to Eastman Kodak Industrial X-Ray Film, Type M which has been exposed in the same manner and processed in an Elonhydroquinone developer for 5 min. at 20 C.
- EXAMPLE 2 A coarse-grained silver bromoiodide (99:1) emulsion is prepared according to the procedure described in Example except that the precipitation is carried out in the presence of 0.01 mg. ammonium chlororhodate/mole Ag. After the digestion step (30 min.), which is carried out in the presence of the above-described thioether ripening agent, the emulsion is salt coagulated, washed thoroughly, redispersed, sulfur and gold sensitized and then stabilized by the addition of a cadmium salt as shown below.
- the speed of the present element is determined and compared to the speed of Kodak Industrial Radiographie Film Type AA.
- the former has a speed of 600 and the latter 100.
- ASA speed is calculated from the customarily used formula +a s We) At an exposure of microsecond to white light, the ASA value is about 8000, of the present element.
- EXAMPLE 4 Employing a non-integral lead foil Du Pont Industrial Type luminescent screen, comparative tests are conducted on processed Eastman Kodak Industrial X-Ray Film Type M, an extra fine grain emulsion of high contrast but not thioether ripened emulsion and the radiographic element of the present invention after exposure. Processing is accomplished for M Type film in an Elon-hydroquinone developer for 5 minutes at 20 C. in order to obtain optimum speed. The present element is processed utilizing its incorporated developer system and the speed comparisons indicate a 60 fold increase in speed of the paper element of the invention over the Type M film. The mottle and physical characteristics of the present element is likewise superior.
- a suitable binder comprising a blend of copolymers of ethyl acrylate, chloroethyl vinyl ether with a poly(alkyl methacrylate) in a coating coverage of about 14.1 parts of pigment, i.e., phosphor, to hinder.
- a photographic element comprising an opaque paper support coated with a radiation sensitive layer comprising from about 350 to about 450 mg./ft. of a hydrophilic colloid and from about 100 to about 200 mg./ft. of silver halide grains precipitated in the presence of a rhodium salt and thioether ripened, and, added to said grains, a stabilizing concentration of a salt of a polyvalent metal ion and a luminescent screen comprising a heavy metal containing luminescent phosphor.
- the element of claim 1 further comprising one or more silver halide developing agents.
- a process for obtaining a high quality radiographic image of a subject which comprises exposing to X-rays or gamma-rays said subject in proximate contact with a radiographic element comprising an opaque paper support, a radiation sensitive layer comprising a hydrophilic colloid in a coating concentration of from about 350 to about 400 mg./ft. in which is dispersed a radiation-sensitive amount of silver halide in a coverage of from about 100 to about 200 mg./ft. said silver halide precipitated in the presence of a rhodium salt thioether ripened and added to said grains, a stabilizing concentration of a salt of a polyvalent metal ion.
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Abstract
DISCLOSED ARE IMPROVED RADIATION-SENSITIVE IMAGE RECORDING ELEMENTS PARTICULARLY USEFUL IN NON-DESTRUCTIVE TESTING WHICH ELEMENTS COMPRISE A SUPPORT CARRYING A THIOETHER RIPENED, POLYVALENT METAL ION STABILIZED RADIATIONSENSITIVE SILVER HALIDE LAYER OF LOW COATING DENSITY DISPERSED IN A HYDROPHILIC COLLOID LAYER OF SUBSTANTIALLY HIGHER COATING DENSITY. THE SILVER HALIDE GRAINS ARE COARSE GRAINED AND THE ELEMENTS CAN OPTIONALLY CONTAIN INCORPORATED DEVELOPER AGENTS AND CAN OPTIONALLY BE COMBINED WITH INTEGRAL OR NON-INTEGRAL LUMINESCENT PHOSPHOR-CONTAINING INTENSIFYING SCREENS. PROCESS FOR NON-DESTRUCTIVE TESTING AND IMAGE RECORDING ARE LIKEWISE DISCLOSED.
Description
United States Patent 3,737,313 PAPER RADIOGRAPHIC ELEMENT CONTAINING SILVER HALIDE GRAINS RHODIUM SALT SEN- SITIZED, THIOETHER RIPENED AND POLY- VALENT METAL ION STABILIZED William J. Rosecrants, Brockport, and Frederick A. Pomeroy, Rochester, N.Y., assignors to Eastman Kodak Company, Rochester, N.Y. No Drawing. Filed June 17, 1971, Ser. No. 154,164
Int. Cl. G03c 1/92, 5/04 US. Cl. 9627 R 8 Claims ABSTRACT OF THE DISCLOSURE Disclosed are improved radiation-sensitive image recording elements particularly useful in non-destructive testing which elements comprise a support carrying a thioether ripened, polyvalent metal ion stabilized radiationsensitive silver halide layer of low coating density d1spersed in a hydrophilic colloid layer of substantially higher coating density. The silver halide grains are coarse grained and the elements can optionally contain incorporated developer agents and can optionally be combined with integral or non-integral luminescent phosphor-containing intensifying screens. Processes for non-destructive testing and image recording are likewise disclosed.
BACKGROUND OF THE INVENTION Field of the invention This invention relates to radiographic image-recording elements and to processes employing such materials. In one aspect this invention relates to radiographic elements comprising single-sided silver halide coatings and optionally containing luminescent intensifying screens. In another aspect this invention relates to radiographic recording systems primarily designed for non-destructive testing and industrial use, which systems contain low silver content which unexpectedly provides improved characteristics to said systems.
Description of the prior art In recent years the growth of mass production methods and trends toward automation of industrial processes have made necessary the rapid and large scale examination and testing of components and assemblies produced by such methods. By such testing, a manufactured item of equipment can be examined in order to determine the nature of its future use and to provide an estimate of its expected working life. One particular method of testing involves the examination of articles by procedures which do not impair the usefulness for future applications of the article itself. This nondestructive testing includes the use of radiological methods, mechanical methods, electrical and magnetic methods, visual methods, and the like. Regardless of the type of testing employed, they are all interested in defect detection and location. The composition, size and location of components and the particular physical state of the article under test likewise play an important role in the selection of testing methods employed. While the versatility of radiography as an inspectional method is a most outstanding feature, there have been substantial limitations on its use, which limitations have been primarily determined by the types of material examined and the type of flaw sought to be detected.
As a practical matter, however, radiographic material has been selected primarily on the basis of balancing the opposing factors of high quality in the image recorded and short exposure time to the object being tested. For example, a high quality film requires a slower, finer grained element and where a short exposure time is sought, a faster element would be required. In the past, this demand for high radiographic quality or short exposure time has found general acceptance by employing radiographic films usually coated on a cellulose acetate support and coated on each side with a radiation sensitive material, such as silver halide. With the increased cost of silver and the great need for more routine testing of mass produced items, cost becomes an important factor along with the faithful reproduction of the object tested. Furthermore, an image of lasting quality is an essential requirement so that good contrast and high photographic quality are important aspects in industrial radiographic elements. Heretofore, the emphasis on critical examination of large and sometimes inaccessible metal objects has been largely accomplished by employing radiographic films having the qualities of good definition, high contrast, maximum density and moderate developing time. It is not surprising therefore that fine grain, high contrast films such as Kodak Industrial X-ray film Type M have been developed for use in direct exposure or with lead foil screens having a silver coverage on each side of their supports of about 900 milligrams/ft. This has led to a general acceptance that the best type of industrial radiographic element is one which is thickly coated with a fine grain silver halide in order to give high contrast and reduce the general exposure time.
Nevertheless, there has been a continuing and unsatisfied need for a radiographic element particularly suitable for nondestructive testing, which element is relatively inexpensive, highly sensitive to direct and screen type exposure and is capable of providing readily accessible images of high quality on site, that is, away from the laboratory darkroom.
It could not have been expected that an improved radiographic system could be achieved by employing a thinner, that is, less densely coated silver halide element having extremely good contrast and high speed. This unexpected aspect is particularly so in the utilization of single sided elements rather than the widely used double coated elements.
It has been known to use improved precipitation methods and stabilization methods along with techniques in ripening stages in order to produce high speed, high contrast emulsions. For example, in US. Patent 3,531,289, issued Sept. 29, 1970 to Wood various thioether and rhodium salts are utilized during the emulsification step and the digestion step to provide an improved process for making developing-out type photographic emulsions. Likewise, in US. Patent 3,488,709, issued Jan. 6, 1970 to Sidebotham and in US. Pat. 3,574,625, issued Apr. 13, 1971 to Bacon, various polyvalent metal ions such as divalent, trivalent and tetravalent metal ions are utilized to stabilize the silver halide emulsions after the halide has been precipitated.
Those skilled in the art will readily appreciate that not all high contrast and fast emulsions can be utilized for radiographic applications. For example, high speed projection emulsions such as thoseparticularly useful in photographic printing papers like enlarging papers, or designed for typesetting use, such as those disclosed in Sidebotham (US. 3,488,709) are unsuited for radiographic use because emulsion streaking and structure and quantum mottle, unobjectional for enlargements and noncontact application, are wholly intolerable for reproducing radiographic images in nondestructive testing.
SUMMARY OF THE INVENTION In accordance with the present invention there is provided an improved photographic image-recording element which comprises a support bearing one sided thereof a radiation sensitive silver halide layer of low coating density dispersed in a hydrophilic colloid of a proportionately higher coating density. The element described herein is possessed of high speed, high contrast, and extraordinary physical characteristics which render it uniquely adaptable to industrial radiography and in particular the nondestructive testing of metal objects. The element sodescribed can contain an incorporated developer and likewise can comprise an integral or non-integral luminescent intensitfying screen to enhance the image forming process. This element provides unexpected improvements in the marked decrease in quantum mottle without impairing the intricately balanced system of'speed, image sharpness and contrast at the expense of prolonged exposure to radiation such as X-rays and gamma rays.
It is one object of the present invention to reduce the quantum mottle of radiographic products and systems without impairing sharpness or speed of said elements.
It is another object of this invention to provide improved photographic elements and, in particular, radiographic elements and processes employing said elements by providing unexpectedly superior image recording characteristics therein.
It is yet another object of this invention to provide a unique product for the nondestructive testing of materials which product comprises a combination of thickened hydrophilic colloid layer having dispersed therein a decreased coverage of light sensitive silver halide.
It is yet another object of this invention to provide a vastly improved nondestructive testing device for indus trial radiography which comprises a paper radiographic element capable of producing a high quality image quickly, conveniently, inexpensively and accurately.
Still other objects of this invention will become apparent to those skilled in the art from the reading of the specification and examples which follow.
DESCRIPTION OF PREFERRED EMBODIMENTS In accordance with this invention the above and other objects are attained with a radiographic element comprising an incorporated developer layer, a radiation sensitive layer comprising (a) a thioether ripened silver halide emulsion precipitated in the presence of a rhodium salt and (b) a stabilizing amount of a polyvalent metal salt, i.e., divalent, trivalent or tetravalent metal salt, and a hydrophilic colloid containing overcoat layer. The thioether-ripened silver halide grains useful in the present invention include those described in U.S. Pat. 3,271,157 issued Sept. 6, 1966 to McBride and those disclosed in U.S. Pat. 3,531,289, issued Sept. 29, 1970 to Wood. The rhodium salts useful in this invention can be any suitable rhodium salt including ammonium chlororhodate, rhodium chloride, and the like. In addition, still other salts such as K IrCl Bi(NO -5H O; H PtCl K IrCl and K O Cl are effective as are other salts of arsenic, gold, antimony and various mixtures thereof.
The polyvalent metals such as those di-, tri-, and tetravalent metals and their salts which enhance the sensitivity and speed of the silver halide grains include trivalent antimony, bismuth, arsenic, gold, iridium, rhodium and the like. Tetravalent metal ions include platinum, osmium, iridium and the like. Divalent metal ions include cadmium such as cadmium chloride, cadmium nitrate, and zinc, like zinc nitrate and various manganese salts and the like, The element so-described comprises a support bearing a radiaiton sensitive layer containing silver halide grains dispersed in a hydrophilic colloid and precipitated in the presence of a rhodium salt, and added to said already formed grains, a stabilizing concentration of a salt of a poly-valent i.e. a di-, trior tetra valent metal ion, the improvement comprising employing a coating concentration of from about 350 to about 450 ing/ft. of said hydrophilic colloid and from 100 to about 200 mg./ft. of said silver halide. Particularly good results are obtained with a photographic element, and particularly a radiographic element, i.e. one which is radiation sensitive comprising a support bearing a layer comprising a hy r philic colloid in a. concentration from about 350 to about 450 rug/ft. in which is dispersed a concentration of silver in a coverage i.e. a coating density of less than about 200 mg./ft. but in a concentration suflicient to provide radiation sensitivity. This improved radiographic element of high image quality comprises a support bearing a high speed, high contrast low silver halide containing layer, said silver halide dispersed in a hydrophilic colloid coated at a density of about 350 to about 450 mg./ft. By high contrast is meant that value equal to the difference between the densities of two areas of the sensitive layer after exposure and processing. In the present invention the contrast is about 4 to about 9 and preferably about 4.5 to about 5.5. In a preferred embodiment it has been found that the above described radiographic element provides a high speed, high contrast image in a short time by incorporating in the above described element suitable developing agents.
In yet another embodiment of the present invention there is provided a process for obtaining a high quality radiographic image of a test subject which comprises exposing to a radiation source, said subject in proximate contact, i.e. indirect contact or in close relation therewith, a radiographic element comprising a support hearing a layer comprising a hydrophilic colloid laid down in a coating concentration of from about 350 to about 450 mg./ft. in which is dispersed a radiation sensitive amount of silver halide in a coverage of less than about 200 mg./ ft. and preferably from about mg./ft. to about mg./ft.
In the typical radiographic element designed for medical application, there is generally provided a coarse or large size radiation sensitive silver halide grain such as a silver bromoiodide grain, in order to provide a fast, light sensitive element so that the exposure to radiation is minimized to the patient. From this, one can readily see that the light or energy absorption requirements of that type of radiation-sensitive element is lower, than the type of element customarily used heretofore for industrial radiography. In particular, the industrial radiograph used of element customarily used heretofore for industrial radiography. In particular, the industrial radiograph used heretofore comprises a fine grain silver halide emulsion or layer containing said fine grains and, in view of the requirement for absorbing as much X-ray or gamma-ray as possible, the element necessarily contains a very high coating density of silver in order to absorb said radiation. Given these minimal requirements for nondestructive testing, the present invention becomes all the more unobvious in that it uses (a) a radiation-sensitive element having coarse silver halide grains typically used for medical radiography and (b) employs said coarse grain in a very light coating density quite unlike heretofore uses elements and processes for industrial radiographs. It is known in the art that by employing paper elements, such as developing paper, printing paper and radiographic paper, it is not possible to utilize extraordinarily high silver coverage, and so when said coverage is reduced, one would normally expect to obtain a dramatic loss of image quality, in view of the fact that the speed is decreased and the D is lowered. As will be seen from the examples hereafter quite the contrary results are achieved in the practice of the present invention. The fact that paper radiographs have historically suffered from inferior sensitivity and poor latitude and difliculty in reproducing copies from an original print is borne out in the text, X-rays in Practice, Sproull (1946) McGraw- Hill, pp. 175 et seq. wherein is stated the chief advantage of X-ray paper over film is that of lesser cost. This conclusion, emphasizing the disadvantages of paper radiographs in that they lack contrast, and that their sensitivity of the flaw detection is poorer than that of film is likewise borne out in An assessment of X-ray Papers for Industrial Radiography Armament Research and Development Establishment, Great Britain, June (1955), Ludgater. Heretofore it has been believed well accepted that the use of fine grain X-ray film was vastly superior for all purposes and particularly in obtaining image sharpness when compared with photographic paper, substituted for said films in radiography.
Mottle is actually believed to be the combination of various components observed in radiographic elements. For example, quantum mottle, the major contributing factor, results from statistical fluctuations in the spatial distribution of the number of photons in the X-ray image while structure mottle results from irregularities in the screen structure. The combination of both of these unwanted defects is called screen mottle and they are particularly apparent whenever a fast-image forming system is used and also as the radiation energy is increased, such as in the high exposure time required in industrial radiography.
By the use of term, radiation, it will be understood to mean the transmission of energy through space such as the diffusion of or transfer of energy through matter. As applied to the present invention, it relates to the stream of X-rays, gamma-rays and the like of (1) relatively short Wave lengths, such as 0.062 A. and (2) hard X-rays of shorter wave lengths of higher penetration, i.e. 0.19-0.43 A. and (3) soft X-rays of low penetration having a wave length of from about 11.9 to about 13.6 A.
The silver halide layers and emulsions used with this invention can comprise silver chloride, silver bromide, silver bromoiodide, silver chlorobromoiodide or mixtures thereof. The emulsions are generally coarse grain, i.e., having a grain size of 0.54.0 1 and can be prepared by any of the well-known procedures, e.g. single jet emulsions, double jet emulsions, such as Lippman emulsions, ammoniacal emulsions, thiocyanate or thioether ripened emulsions such as those described in Nietz et al. U.S. Pat. 2,222,264 issued Nov. 19, 1940; Illingsworth U.S. Pat. 3,320,069 issued May 16, 1967; and McBride U.S. Pat. 3,271,157 issued Sept. 6, 1966. The silver halide is preferably unfogged and contains at least about 50% bromide, less than about 10% iodide and less than about 50% chloride on a molar basis. Preferably the silver halide is a silver bromoiodide containing about 95% to about 99% bromide, i.e., about 5% to about 1% iodide. Surface image emulsions can be used or internal image emulsions such as those described in Davey et al. U.S. Pat. 2,592,250 issued May 8, 1952; Porter et al. U.S. Pat. 3,206,313 issued Sept. 14, 1965; Berriman U.S. Pat. 3,367,778 issued Feb. 6, 1968; and Bacon et al. U.S. Pat. 3,447,927 issued June 3, 1969. Negative type emulsions can be used or direct positive emulsions such as those described in Leerrnakers US. Pat. 2,184,013 issued Dec. 19, 1939; Kendall et al. U.S. Pat. 2,541,472 issued Feb. 13, 1951; Berriman U.S. Pat. 3,367,778 issued Feb. 6, 1968; Schouwenaars British Pat. 723,019 issued Feb. 2, 1955; Illingsworth et al. French Pat. 1,520,821 issued Mar. 4, 1968; Ives U.S. Pat. 2,563,785 issued Aug. 7, 1951; Knott et al. U.S. Pat. 2,456,953 issued Dec. 21, 1948, and Land U.S. Pat. 2,861,885 issued Nov. 25, 1958. The emulsions can be regular grain emulsions such as the type described in Klein and Moisar, J. Phot. Sci., vol. 12, No. 5, September/October 1964, pp. 242251.
The silver halide layers and emulsions used with this invention can be unwashed or washed to remove soluble salts. In the latter case the soluble salts are removed by chill-setting and leaching or the emulsion can be coagulation washed, e.g. by the procedures described in Hewitson et al. U.S. Pat. 2,618,556 issued Nov. 18, 1952; Yutzy et al. U.S. Pat. 2,614,928 issued Oct. 21, 1952; Yackel U.S. Pat. 2,565,418 issued Aug. 21, 1951; Hart et al. U.S. Pat. 3,241,969 issued Mar. 22, 1966; and Waller et al. U.S. Pat. 2,489,341 issued Nov. 29, 1949.
The silver halide layers and emulsions used with this invention can be sensitized with chemical sensitizers, such as with reducing agents; sulfur, selenium or tellurium compounds; gold, platinum or palladium compounds; or combinations of these. Suitable procedures are described 6 in Sheppard et al. U.S. Pat. 1,623,499 issued Apr. 5, 1927; Waller et al. U.S. Pat. 2,399,083 issued Apr. 23, 1946; McVeigh U.S. Pat. 3,297,447 issued Jan. 10, 1967; and Dunn U.S. Pat. 3,297,446 issued Jan. 10, 1967.
This silver halide layers and emulsions used with this invention can contain speed increasing compounds such as polyalkylene glycols, cationic surface active agents and thioethers or combinations of these as described in Piper U.S. Pat. 2,886,437 issued May 12, 1959; Damn et al. U.S. Patent 3,046,134 issued July 24, 1962; Carrol et al. U.S. Pat. 2,944,900 issued July 12, 1960; and Golfe U.S. Pat. 3,294,540 issued Dec. 27, 1966.
The silver halide layers and emulsions used in the practice of this invention can be protected against the production of fog and can be stabilized against loss of sensitivity during keeping. Suitable antifoggants and stabilizers each used alone or in combination include thiazolium salts described in Brooker et al. U.S. Pat. 2,131,038 issued Sept. 27, 1938, and Allen et al. U.S. Pat. 2,694,716 issued Nov. 16, 1954; the azaindenes described in Piper U.S. Pat. 2,886,437 issued May 12, 1959; and Heimbach et al. U.S. Pat. 2,444,605 issued July 6, 1948; the mercury salts as described in Allen et al. U.S. 2,728,663 issued Dec. 27, 1955; the urazoles described in Anderson et al. U.S. Pat. 3,287,135 issued Nov. 22, 1966; the sulfocatechols described in Kennard et al. U.S. Pat. 3,236,652 issued Feb. 22, 1966; the oximes described in Carroll et al. British Pat. 623,448 issued May 18, 1949; nitron; nitroindazoles; the mercaptotetrazoles described in Kendall et al. U.S. Pat. 2,403,927 issued July 16, 1946; Kennard et al. U.S. Pat. 3,266,897 issued Aug. 16, 1966, and Luckey et al. U.S. Pat. 3,397,987 issued Aug. 20, 1968; the polyvalent metal salts described in Jones U.S. Pat. 2,839,405 issued June 17, 1958; the thiuronium salts described in Herz et al. U.S. Pat. 3,220,839 issued Nov. 30, 1965; the palladium, platinum and gold salts described in Trivelli et al. U.S. Pat. 2,566,263 issued Aug. 28, 1951, and Yutzy et al. U.S. Pat. 2,597,915 issued May 27, 1952.
The radiographic elements of this invention can contain an incorporated developer comprising one or more developing agents such as hydroquinones, catechols, aminophenols, 3-pyrazolidones, ascorbic acid and its derivatives, reductones and phenylenediamines. Combinations of developing agents can be employed in the practice of the invention. The developing agents can be in a silver halide emulsion and/ or in an other suitable location in the photographic element. The developing agents can be added from suitable solvents or in the form of dispersions as described. in Yackel U.S. Pat. 2,592,368 issued Apr. 8, 1952 and Dunn et al., French Pat. 1,505,778.
The radiographic and other hardenable layers used in the practice of this invention can be hardened by various organic or inorganic hardeners, alone or in combination, such as the aldehydes, and blocked aldehydes, ketones, carboxylic and carbonic acid derivatives, sulfo nate esters sulfonyl halides and vinyl sulfonyl ethers, active halogen compounds, epoxy compounds, aziridines, active olefines, isocyanates, carbodiirnides, mixed function hardeners and polymeric hardeners such as oxidized polysaccharides like dialdehyde starch and oxyguar gum and the like.
The radiographic emulsions and elements described in the practice of this invention can contain various colloids alone or in combination as vehicles, binding agents and various layers. Suitable hydrophilic materials include both naturally-occurring substances such as proteins, for example, gelatin, gelatin derivatives, cellulose derivatives, polysaccharides such as dextran, gum arabic and the like; and synthetic polymeric substances such as water soluble polyvinyl compounds like poly(vinylpyrrolidone), acrylamide polymers and the like.
The described radiographic emulsion layers and other layers of a photographic element employed in the practice of this invention can also contain alone or in combination with hydrophilic water permeable colloids, other synthet is polymeric compounds such as dispersed vinyl compounds such as in latex form and particularly those which increase the dimensional stability of the photographic materials. Suitable synthetic polymers include those described, for example, in Nottorf U.S. Pat. 3,142,568 issued July 28, 1964; White U.S. Pat. 3,193,386 issued July 6, 1965; Houck et a1. U.S. Pat. 3,062,674 issued Nov. 6, 1962; Houck et al. U.S. Pat. 3,220,844 issued Nov. 30, 1965; Ream et al. U.S. Pat. 3,287,289 issued Nov. 22, 1966; and Dykstra US. Pat. 3,411,911 issued Nov. 19, 1968; particularly effective are those water-insoluble polymers of alkyl acrylates and methylacrylates, acrylic acid, sulfoalkyl acrylates or methacrylates, those which have crosslinking sites which facilitate hardening or curing, those having recurring sulfobetaine units as described in Dykstra Canadian Pat. 774,054.
The radiographic elements used with this invention can contain antistatic or conducting layers, such layers can comprise soluble salts, e.g. chlorides, nitrates, etc., evaporated metal layers, ionic polymers such as those described in Minsk U.S. Pat. 2,861,056 issued Nov. 18, 1958 and Sterman et al., U.S. Patent 3,206,312 issued Sept. 14, 1965 or insoluble inorganic salts such as those described in Trevoy U.S. Pat. 3,428,451 issued Feb. 18, 1969.
The radiographic layers employed in the practice of this invention can contain plasticizers and lubricants such as polyalcohols, e.g. glycerin and diols of the type described in Milton et al., U.S. Patent 2,960,404 issued Nov. 1, 1966; fatty acids or esters such as those described in Robijns U.S. Pat. 2,588,765 issued Apr. 11, 1952, and Duane U.S. Pat. 3,121,060 issued Feb. 11, 1964; and silicone resins such as those described in Du Pont British Patent 955,061 issued Apr. 15, 1964.
The radiographic layers employed in the practice of this invention can contain surfactants such as saponin; anionic compounds such as the alkyl aryl sulfonates described in Baldsiefen U.S. Pat. 2,600,831 issued June 17, 1952; amphoteric compounds such as those described in Ben-Ezra U.S. Pat. 3,133,816 issued May 19, 1964; and water soluble adducts of glycidol and an alkyl phenol such as those described in Olin Mathieson British Pat. 1,022,878 issued Mar. 16, 1966.
The radiographic elements employed in the practice of this invention can contain matting agents such as starch, titanium dioxide, zinc oxide, silica, polymeric beads including beads of the type described in Jelley et al., U.S. 'Pat. 2,992,101 issued July 11, 1961 and Lynn U.S. Pat. 2,701,245, issued Feb. 1, 1955.
The radiographic elements used in this invention can contain brightening agents including stilbenes, tniazines, oxazoles and coumarin brightening agents. Water soluble brightening agents can be used such as those described in Alberz et al., German Pat. 972,067 and McFall et al., U.S. Pat. 2,933,390 issued Apr. 19, 1960 or dispersions of brighteners may be used such as those described in Jansen German Pat. 1,150,274, Oetiker et al., U.S. Pat. 3,406,070 issued Oct. 15, 1968 and Heidke French Pat. 1,530,244.
Spectral sensitizing dyes can be used conveniently to confer additional sensitivity to the radiation sensitive silver halide emulsion of the radiographic elements of the invention. For instance, additional spectral sensitization can be obtained by treating the emulsion with a solution of a sensitizing dye in an organic solvent or the dye can be 'added in the form of a dispersion as described in Owens et al. British Pat. 1,154,781 issued June 11, 1969. For optimum results, the dye is either added to the emulsion as a final step or at some earlier stage.
'Sensitizing dyes useful in sensitizing such emulsions are described, for example, in Brooker et al. U.S. Pat. 2,526,- 632 issued Oct. 24, 1950; Sprague U.S. Pat. 2,503,776 issued Apr. 11, 1950; Brooker et al. U.S. Pat. 2,493,748 issued J an. 10, 1950; and Faber et al. U.S. Pat. 3,384,486 issued May 21, 1968. Spectral sensitizers which can be used include the cyanines, merocyanines, complex (tri or tetranuclear) merocyanines, complex (tri or tetranuclear) cyanines, holopolar cyanines, styryls, hemicyanines (e.g. enamine hemicyanines), oxonols and hemioxonols.
Dyes of the cyanine classes can contain such basic nuclei as the thiazolines, oxazolines, pyrrolines, pyridines, oxazoles, thiazoles, selenazoles and imidazoles. Such nuclei can contain alkyl, 'alkylene, hydroxyalkyl, sulfoalkyl, carboxyalkyl, aminoalkyl and enamine groups and can be fused to carbocyclic or heterocyclic ring systems either unsubstituted or substituted with halogen, phenyl, alkyl, haloalkyl, cyano, or alkoxy groups. The dyes can be symmetrical or unsymmetrical and can contain alkyl, phenyl, enamine or heterocyclic substitutents on the methine or polymethine chain.
The merocyanine dyes can contain the basic nuclei mentioned above as Well as acid nuclei such as thiohydantoins,
.rhodanines, oxazolidenediones, thiazolidenediones, barbituric acids, thiazolineones, and malononitrile. These acid nuclei can be substituted with alkyl, alkylene, phenyl, carboxyalkyl, sulfoalkyl, hydroxyalkyl, alkoxyalkyl, alkylamino groups, or heterocyclic nuclei. Combinations of these days can be used, if desired. In addition, supersensitizing addenda which do not absorb visible light can be included, for instance, ascorbic acid derivatives, azaindenes, cadmium salts, and organic sulfonic acids as described in McFall et al., U.S. Pat. 2,933,390 issued Apr. 19, 1960, and Jones et al. U.S. Pat. 2,937,089 issued May 17, 1960.
The various layers, including the radiographic layers, employed in the practice of this invention can contain light absorbing materials and filter dyes such as those described in Sawdey U.S. Pat. 3,253,921 issued May 31, 1966; Gaspar U.S. Pat. 2,274,782 issued Mar. 3, 1942; Silberstein et al. U.S. Pat. 2,527,583 issued Oct. 31, 1950, and VanCampen U.S. Pat. 2,956,879 issued Oct. 18, 1960. If desired, the dyes can be mordanted, for example, as described in Milten et al., U.S. Pat. 3,282,699 issued Nov. 1, 1966.
The sensitizing dyes and other addenda used in the practice of this invention can be added from water solutions or suitable organic solvent solutions can be used. The compounds can be added using various procedures including those described in Collins et al., U.S. Pat. 2,912,343 issued Nov. 10, 1959; McCrossen et al., U.S. Pat. 3,342,605 issued Sept. 19, 1967; Audran U.S. Pat. 2,996,287 issued Aug. 15, 1961 and Johnson et al., U.S. Pat. 3,425,835 issued Feb. 4, 1969.
The radiographic layers used in the practice of this invention can be coated by various coating procedures including dip coating, air knife coating, curtain coating, or extrusion coating using hoppers of the type described in Beguin U.S. Pat. 2,681,294 issued June 15, 1954. If desired, two or more layers may be coated simultaneously by the procedures described in Russell U.S. Pat. 2,761,791 issued Sept. 4, 1956 and Wynn British Pat. 837,095. This invention also can be used for silver halide layers coated by vacuum evaporation as described in British Pat. 968,- 453 and LuValle et al., U.S. Pat. 3,219,451 issued Nov. 23, 1965. a
This invention can be used with elements designed for color photography, for example, elements containing color-forming couplers such as those described in Frohlich et al., U.S. Pat. 2,376,679 issued May 22, 1945; Jelley et al., U.S. Pat. 2,322,027 issued June 15, 1943; Fierke et al., U.S. Pat. 2,801,171 issued July 30, 1957; Godowsky U.S. Pat. 2,698,794 issued Jan. 4, 1955; Barr et al., U.S. Pat. 3,227,554 issued Jan. 4, 1966; and Graham et al., U.S. Pat. 3,046,129 issued July 24, 1962; or elements to be developed in solutions containing color-forming couples such as those described in Mannes et al., U.S. Pat. 2,252,718 issued Aug. 19, 1941; Carroll et al., U.S. Pat. 2,592,243 issued Apr. 18, 1952; and Schwan et al., U.S. Pat. 2,950,970 issued Aug. 30, 1966; and in false-sensitized color materials such as those described in Hanson U.S. Pat. 2,763,549 issued Sept. 18, 1956.
Radiographic elements prepared according to this invention can be processed by various methods including processing in alkaline solutions containing conventional developing agents such as hydroquinones, catechols, aminophenols, 3-pyrazolidones, phenylenediamines, ascorbic acid derivatives, hydroxylamines, hydrazines, reductones and the like; web processing such as described in Tregillus et al. U.S. Pat. 3,179,517 issued Apr. 20, 1965; stabilization processing as described in Russell et al. Stabilization Processing of Films and Papers, PSA Journal, vol. 163, August 1950; monobath processing as described in Levy Combined Development and Fixation of Photographic Images with Monobaths, Phot. Sci. and Eng., vol. 2, No. 3, October 1958, and Barnes et al. U.S. Pat. 3,392,019 issued July 9, 1968. If desired, the photographic elements of this invention can be processed in hardening developers such as those described in Allen et al. U.S. Pat. 3,232,761 issued Feb. 1, 1966; in roller transport processors such as those described in Russell et al. U.S. Pat. 3,025,779 issued Mar. 20, 1962; or by surface application processing as described in Example 3 of Kitze U.S. Pat. 3,418,132 issued Dec. 24, 1968.
This invention can be used with elements designed for colloid transfer processes such as described in Yutzy et al., U.S. Pat. 2,716,059 issued Aug. 23, 1953; silver salt ditfusion transfer processes such as described in Rott U.S. Pat. 2,352,014 issued June 20, 1944; Land U.S. Pat. 2,543,181 issued Feb. 27, 1951; Yackel et al. U.S. Pat. 3,020,155 issued Feb. 6, 1962; and Land U.S. Pat. 2,861,- 885 issued Nov. 25, 1958; color image transfer processes such as described in Rogers U.S. Pats. 3,087,817 issued Apr. 30, 1963; 3,185,567 issued May 25, 1965; and 2,983,606 issued May 9, 1961; Weyerts et al. U.S. Pat. 3,253,915 issued May 31, 1966; Whitmore et a1 U.S. Pat. 3,227,550 issued Jan. 4, 1966; Barr et al. U.S. Pat. 3,277,- 551 issued Jan. 4, 1966; Whitmore et al. U.S. Pat. 3,227,552 issued Jan. 5 ,1966; and Land U.S. Pats. 3,415,- 644 issued Dec. 10, 1968; 3,415,645 issued Dec. 10, 1968; and 3,415,646 issued Dec. 10, 1968; and imbibition transfer processes as described in Minsk U.S. Pat. 2,882,156 issued Apr. 14, 1959.
This invention may be used in elements designed for recording print out images as described in Fallesen U.S. Pat. 2,369,449 issued Feb. 13, 1945 or Bacon et al. U.S. Pat. 3,447,927 issued June 3, 1969; elements designed for processing by heat as described in Sorensen et al. U.S. Pat. 3,152,904 issued Oct. 13, 1964; Morgan et al. U.S. Pat. 3,457,075 issued July 22, 1969; Stewart et al. U.S. Pat. 3,312,550 issued Apr. 4, 1967 and Colt U.S. Pat. 3,418,122 issued Dec. 24, 1968.
This invention can be used in elements designed for physical development such as those described in Agfa British Pat. 920,277 and Gilrnan et al. British Pat. 1,131,238.
Hydrophilic colloid materials which can be used in the practice of the invention include various waterpermeable binder vehicles which materials can be suspended in colloidal dispersions. Hydrophilic colloids suitable as binder vehicles and layers include proteinaceous compounds such as, for example, gelatin, colloidal albumin and other hydrophilic colloids such as, for example, polyvinyl compounds, cellulose derivatives, acrylamide polymers, etc., though gelatin materials are preferred. The high molecular weight materials for binder vehicles and layers which are generally consider soluble in aqueous solutions and do not form small discrete particles when mixed with an aqueous gelatin emulsion, as can be determined upon observation of a photomicrograph, can be considered hydrophilic colloids for purposes of this invention.
The phosphors in the X-ray intensifying screens possess the characteristic of having a substantial part, that is, more than half, of their total spectral emission at less than about 410 nm. This emission is substantially in the ultraviolet range of the spectrum and it has been found that a host matrix comprising at least one of certain heavy metal phosphors are particularly useful therefor. Such phosphors have a physical density greater than at least about 3.5 and preferably greater than 3.9. However, particularly effective novel combinations in the practice of this invention use heavy metal phosphors, including those made from the lanthanide group of the periodic table. The latter rare earth elements have an atomic number in the range of between 58 to 71 and include lanthanum, cerium, Samarium, gadolinium and the like. Particularly eifective heavy metal phosphors are those such as lanthanideor leadactivated BaSO and BaSrSO such as europium activated BaSrSO lead-activated barium silicates, gadolinium-activated yttrium oxide, and barium fluoride, barium fluoride chloride and the like. Said phosphors can be further activated by rare earth activators alone and in combination. These phosphors can be prepared by a number of ways, such as set forth in Belgian Pat. 703,998 issued Mar. 18, 1969 to Luckey; in Buchanan et al. J. Applied Physics, vol. 39, pp. 4342-4347 (1968) and in Clapp and Ginth'er, 1., of the Optical Soc. of America, vol. 37, No. 1, pp. 355-62 (1947). These phosphors can be used in screens which are either integral or non-integral with radiographic image forming elements which elements have single coated light sensitive layers.
A preferred use of the radiographic elements necessary to the invention herein is in combination with radiographic intensifying screens particularly because the absorption of X-rays by the phosphor host is so high. In fact, the absorption of X-ray energy by the radiographic screens comprising certain phosphors is so high that single sided radiographic systems can be employed which systems form part of the present invention. These single-sided radiographic systems provide such extraordinary sharpness and high speed that they are equal or superior to similar results obtained by conventional double-sided systems. Among the various phosphors exhibiting the desirable luminescence is the terbium-activated lanthanum oxysulfide which has a negligible after-glow and whose green emission makes it particularly suitable for fluoroscopic and radiographic application.
The intensifying fluorescent screens, which can form part of the radiographic element of our invention, consist essentially of phosphors which can be dispersed or suspended in a suitable binder such as those set forth in U.S. Pats. 3,300,310 and 3,300,311 supra. which employ a water-soluble copolymer of alkylacrylate and acrylic acid, copolymers of vinyl chloride and vinyl acrylate, polyvinyl butyral as set forth in German Pat. 1,186,332 issued I an. 28, 1965, to Patten et al., a coherent film-forming macromolecular polymer binder such as resins, polymers or copolymers of polycarbonate which comprise recurring carbonate units in the polymer chain, and the like, polymers of acrylic acid esters containing small percentages of a chlorine-containing derivative, such as acrylonitrile copolymers such as Hycar (a trademark of BF. Goodrich Chemical Company for the thus-described dry rubber polymers). Among preferred binders are those screenbinders including blends of copolymers of ethyl acrylate, chloro ethyl vinyl ether with a poly alkyl methacrylate and polyurethane elastomers. The phosphors can be present in the binder in a wide variety of ratios such as, for example, from about 30:1 to about 4:1 and preferably in the range of about 16:1 to about 6:1. The coverage of the phosphor can vary over a wide range. Effective coverage can be determined through experimentation. A preferred coverage of said phosphor in the screen is in a range from about 15 to about 150 grams/ftF. With respect to general purpose screens good results are achieved with a coverage in the range of about 50 to grams/ft. and with respect to high definition screens a coverage of from about 15 to 35 grams/ft? yields good results. Likewise, these screens can be coated in a variety of ways such as directly over the photographic layer or on both sides of a double coated or single coated element. Intermediate 1 l layers, such as stripping layers, protective or overcoat layers, can likewise be employed between or over the X-ray emulsion layer and the intensifying screen. Said layers can comprise hydrophilic colloid material such as gelatin, gelatin derivatives, cellulose esters, alkyl acrylatecontaining polymers and the like.
The radiographic elements of our invention employ, in addition to the phosphor-containing intensifying screen, a suitably supported image recording layer such as one comprising silver halide as disclosed hereinbefore. The radiographic elements and combinations so described can be constructed such that the photographic elements are either separate, i.e. non-integral or integral, i.e. as a separate distinct layer of an element comprising a silver halide emulsion coated onto a support with the intensifying screen. Said silver halide can be present in a layer or coating such as a single coating on one side of a support. Suitable supports are those having the properties to permit their ready passage through a rapid automatic processor if desired. Said support should, therefore, be reasonably flexible and preferably able to maintain the dimensional stability and integrity of the various coatings thereon. Typical supports are fibrous materials used as supports such as cards or paper which are coated with ocolefin polymers, particularly polymers of a-olefins containing two to ten carbon atoms, as exemplified by polyethylene, polypropylene, ethylene-butene copolymers, and the like, give good results. In addition, if desired, said supports can comprise light absorbing materials either within the support itself, on a layer over and/or under said support, or both.
The thickness of said support can vary as is well-known in the art in order to practice effectively our invention.
The silver halide can comprise varying amounts of silver chloride, silver iodide, silver bromide, silver chlorobromide, silver brornoiodide and the like. Particularly good results are obtained with gelatino silver bromoiodide emulsions in which the average grain size of the silver brornoiodide crystals is in the range of about 0.5 to about 5 microns. These layers are applied by means well-known in the art.
The photographic silver halide coatings can also contain additional additives, particularly those known to be beneficial in photographic emulsions. For example, they can contain speed-increasing compounds, for example, onium salts, such as quaternary ammonium or ternary sulfonium salts, polyalkylene glycols, thioethers and the like. The photographic silver halide coatings can be stabilized with mercury compounds, azaindenes, quaternary benzothiazolium compounds, hydroxy substituted aromatic compounds, and the like.
The photographic silver halide elements which are part of the radiographic combinations described herein provide very good results in image sharpness without absolute need for any dyes or other light absorbing materials. While there is no need for employing dyes or other light absorbing materials in either the film, the screen, or both, extraordinary results can be obtained by using such dyes and light absorbing materials. Where used, light absorbing dyes and materials can be in the emulsion layer or in an auxiliary layer such as a layer coated between the support and the emulsion layer, or the light absorbing dyes and materials can be included in both the emulsion and the auxiliary layer. These elements can also contain inert particles such as those often employed as matting agents in photographic elements. Suitable materials of this type include, for example, particles of silicon dioxide, glass, starch, polymethyl methacrylate and the like. Such inert particles are often included in an emulsion layer alone and in combination.
These elements can likewise contain various protective overcoats such as those which comprise colloidal silica in an overcoat comprising gelatin and at least another hydrophilic colloid, including gelatin-compatible acrylic.
. 12 polymers which improve various physical characteristics and optical clarity.
Processing can be elfected'not only by utilizing the incorporated developer system but also in a variety of other ways including the multi-tank manual methods but preferably in a unidirectional, multi-roller high speed processing apparatus described in Belgian Patent 700,301 issued Aug. 31, 1967, to Barnes et a1. These processes can be eifected and the combinations of this invention can be processed respectively according to US. Patent 3,232,761 issued Feb. 1, 1966, to Allen and Burness, Reissue 26,601. Y
The silver-containing film-screen combinations of our invention can likewise be used with unexpectedly good radiographic results in solvent transfer systems such as where single and double coatings are employed. In addition where positive images are so obtained they are easily converted to negative microfilm images either during or after processing. Equally good results are obtained when these novel combinations contain color couplers, such as those described in British Patent 799,588 issued Aug. 13, 1958, to Whitmore and Elins, and by using these novel combinations and processes in color film-containing systems. 3
As a result of our novel phosphors and screens containing them, radiographic combinations are used effectively in recording X-ray images, and there is unexpectedly provided screen-film combinations having improved sharpness, and with vastly increased speed.
EXAMPLE 1 A typical coarse-grained, silver brornoiodide (99:1) emulsion suitable for use in X-ray film elements is prepared by employing the double-jet" technique. An aqueous solution of potassium bromide and potassium iodide and another aqueous solution of silver nitrate are added simultaneously over a period of 10 minutes to an aqueous gelatin solution at 65.6 C. A thioether ripening agent, 1,8-dihydroxy-3,6-dithiooctane (10.9 g./mole Ag) is added to the precipitated emulsion which is then digested for approximately 30 minutes, salt 'coagulated, washed thoroughly, redispersed and sulfur and gold sensitized. The chemically sensitized emulsion is combined with the following solutions:
Amt./ 1.14 moles Ag, ml. Methanol solution containing 0.1% by weight anhydro 5,6 dichloro 1,3 diethyl 3 (3- sulfopropyl)benzimidazolooxacarbocyanine hydroxide 40.0 Aqueous solution containing 0.67% by weight 4- hydroxy 6 methyl-l,3,3a,7-tetraazindene sodium salt 75.0 Aqueous solution containing 2.8% by weight p-toctylphenoxyethoxyethyl sodium sulfonate 100.0
The bottom layer is coated on paper support at 6.90 g. solution/ft therefore resulting in an incorporated developer layer containing approximately 222 mg. gelatin/ ft. 76 mg. methyl hydroquinone/ft. and 15 mg. 1- phenyl-3-pyrazolidone/ft.
The radiographic element is then overcoated with a gelatin containing composition at 5.85 g. solution/fe thereby resulting in a layer containing approximately 53 mg. gelatin/ft? The dried multilayer radiographic element is exposed to X-ray radiation (110 kv., 10 ma.) for 15 seconds at a distance of 3 feet and then processed by passing the exposed element through an Eastman Kodak Ektamatic Processor which activates the incorporated developer element and stabilize it. The processed element is assigned a relative speed of 100 and is equal in speed to Eastman Kodak Industrial X-Ray Film, Type M which has been exposed in the same manner and processed in an Elonhydroquinone developer for 5 min. at 20 C.
EXAMPLE 2 A coarse-grained silver bromoiodide (99:1) emulsion is prepared according to the procedure described in Example except that the precipitation is carried out in the presence of 0.01 mg. ammonium chlororhodate/mole Ag. After the digestion step (30 min.), which is carried out in the presence of the above-described thioether ripening agent, the emulsion is salt coagulated, washed thoroughly, redispersed, sulfur and gold sensitized and then stabilized by the addition of a cadmium salt as shown below.
Amt/1.14 moles Ag., Ml. Aqueous solution containing 5.67% by weight 4- hydroxy-6-methyl-1,3,3a,7-tetrazaindene sodium salt 75.0 Aqueous solution containing 30.5% by Weight cadmium bromide 200.0 Polyacrylamide 200.0 Aqueous solution containing 2.8% by weight p t octylphenoxyethoxyethyl sodium sulfonate spreading agent 10.0
and coated with 403 mg. gelatin and 150 mg. Ag/ft. over an incorporated developer layer which originated from a composition containing the following compounds and solutions:
Gelatin g Aqueous solution containing 6.43% by weight sodium formaldehyde bisulfite, 3.38% by weight hydroquinone and 3.0% by weight methyl hydroquinone liters Aqueous methanol solution containing 1.0% by weight l-phenyl-3-pyrazolidone, 0.28% by weight 5-nitro-1H-indazole and 66.8% methanol liters EXAMPLE 3 The photographic elements described in previous Example 2 and in US. Patent 3,488,709 issued to Sidebotham Jan. 6, 1970, are radiographically exposed and then processed in the same manner as described in Example 2. These elements are compared with the following results:
Ratings: 1=highest, acceptable; 2=motlerate; 3=low; and 4=lo\vest, unsatisfactory.
The speed of the present element is determined and compared to the speed of Kodak Industrial Radiographie Film Type AA. The former has a speed of 600 and the latter 100. ASA speed is calculated from the customarily used formula +a s We) At an exposure of microsecond to white light, the ASA value is about 8000, of the present element.
EXAMPLE 4 Employing a non-integral lead foil Du Pont Industrial Type luminescent screen, comparative tests are conducted on processed Eastman Kodak Industrial X-Ray Film Type M, an extra fine grain emulsion of high contrast but not thioether ripened emulsion and the radiographic element of the present invention after exposure. Processing is accomplished for M Type film in an Elon-hydroquinone developer for 5 minutes at 20 C. in order to obtain optimum speed. The present element is processed utilizing its incorporated developer system and the speed comparisons indicate a 60 fold increase in speed of the paper element of the invention over the Type M film. The mottle and physical characteristics of the present element is likewise superior. The exposure is made against various aluminum castings and a honeycombed stainless steel grid to determine the presence of latent defects. Of the fractures discovered, the prior art film could only show those of a gross nature and in poor contrast while the present element showed various undetected hairline fractures in addition thereto and with considerably good contrast. Equally good results are obtained in the process of recording a radiographic image by employing a variety of luminescent phosphor screens comprising the heavy metal ion and an activator element, e.g., (1) europium activated barium lead sulfate, (2) europium activated gadolinium oxide, (3) and terbium activated lanthanum oxysulfide. All are prepared according to the process described in Belgian Patent 703,998 issued Mar. 18, 1969, to Luekey and are dispersed in a suitable binder comprising a blend of copolymers of ethyl acrylate, chloroethyl vinyl ether with a poly(alkyl methacrylate) in a coating coverage of about 14.1 parts of pigment, i.e., phosphor, to hinder.
The invention has been described in detail 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.
We claim:
1. A photographic element comprising an opaque paper support coated with a radiation sensitive layer comprising from about 350 to about 450 mg./ft. of a hydrophilic colloid and from about 100 to about 200 mg./ft. of silver halide grains precipitated in the presence of a rhodium salt and thioether ripened, and, added to said grains, a stabilizing concentration of a salt of a polyvalent metal ion and a luminescent screen comprising a heavy metal containing luminescent phosphor.
2. The element of claim 1 further comprising one or more silver halide developing agents.
3. The element of claim 1 in which said paper support is resin coated.
4. The element of claim 1 in which said hydrophilic colloid is gelatin.
peed
5. The film screen combination of claim 1 in which said screen is integrally combined with said film.
6. The element of claim 1 in which said silver halide is present as coarse grains of silver bromoiodide.
7. A process for obtaining a high quality radiographic image of a subject which comprises exposing to X-rays or gamma-rays said subject in proximate contact with a radiographic element comprising an opaque paper support, a radiation sensitive layer comprising a hydrophilic colloid in a coating concentration of from about 350 to about 400 mg./ft. in which is dispersed a radiation-sensitive amount of silver halide in a coverage of from about 100 to about 200 mg./ft. said silver halide precipitated in the presence of a rhodium salt thioether ripened and added to said grains, a stabilizing concentration of a salt of a polyvalent metal ion.
8. The process of claim 7 in which said element further comprises one or more silver halide developing agents.
16 References Cited UNITED STATES PATENTS 3,488,709 1/1970 Sidebotham 96-1 10 3,531,290 '9/1970 Litzerman 96-l08 2,887,379 5/1959 Blake et a1 9645.l X 3,531,289 9/1970 Wood 96108 :NORMAN G. TORCHIN, Primary Examiner 10 W. H. LOUIE, JR., Assistant Examiner US. Cl. X.R.
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US15416471A | 1971-06-17 | 1971-06-17 |
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US00154164A Expired - Lifetime US3737313A (en) | 1971-06-17 | 1971-06-17 | Paper radiographic element containing silver halide grains rhodium salt sensitized,thioether ripened and polyvalent metal ion stabilized |
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Cited By (16)
Publication number | Priority date | Publication date | Assignee | Title |
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US3901711A (en) * | 1972-08-31 | 1975-08-26 | Mitsubishi Paper Mills Ltd | Silver halide photographic emulsion containing a gold salt and a polyalkylene oxide |
US3953215A (en) * | 1973-07-16 | 1976-04-27 | Fuji Photo Film Co., Ltd. | Silver halide photographic emulsions |
US4130429A (en) * | 1972-11-03 | 1978-12-19 | Agfa-Gevaert, N.V. | Combination of photosensitive elements suited for use in radiography |
US4130428A (en) * | 1971-11-05 | 1978-12-19 | Agfa-Gevaert, N.V. | Combination of photosensitive elements suited for use in radiography |
US4140531A (en) * | 1975-09-10 | 1979-02-20 | Minnesota Mining And Manufacturing Company | Light-handleable photographic materials |
US4180402A (en) * | 1977-11-28 | 1979-12-25 | Vsesojuzny Gosudarstvenny Nauchno-Issiedovatelsky I Proekthyinstitut Khimo-Forograficheskoi Promyshlennosti | Process for obtaining half-tone picture of irregular structure |
US4232116A (en) * | 1979-01-31 | 1980-11-04 | Minnesota Mining And Manufacturing Company | Light-handleable photographic materials |
EP0023661A2 (en) * | 1979-08-02 | 1981-02-11 | Agfa-Gevaert AG | Photographic silver halide emulsion with a stabilizer, process for its production, photographic recording materials and method of making photographic images |
EP0198634A2 (en) | 1985-04-04 | 1986-10-22 | EASTMAN KODAK COMPANY (a New Jersey corporation) | Quaternized tellurium salt fog inhibiting agents for silver halide photography |
US4973548A (en) * | 1988-08-05 | 1990-11-27 | Eastman Kodak Company | Photographic silver bromoiodide emulsions, elements and processes |
US5248577A (en) * | 1990-08-13 | 1993-09-28 | Eastman Kodak Company | Reactant concentration control method and apparatus for precipitation reactions |
EP0616254A1 (en) * | 1993-03-16 | 1994-09-21 | Minnesota Mining And Manufacturing Company | Rapid-access medical x-ray film and process |
EP0699944A1 (en) | 1994-08-26 | 1996-03-06 | Eastman Kodak Company | Tabular grain emulsions with sensitization enhancements |
EP0699949A1 (en) | 1994-08-26 | 1996-03-06 | Eastman Kodak Company | Ultrathin tabular grain emulsions with dopants at selected locations |
EP0699950A1 (en) | 1994-08-26 | 1996-03-06 | Eastman Kodak Company | Ultrathin tabular grain emulsions with novel dopant management |
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1971
- 1971-06-17 US US00154164A patent/US3737313A/en not_active Expired - Lifetime
Cited By (18)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4130428A (en) * | 1971-11-05 | 1978-12-19 | Agfa-Gevaert, N.V. | Combination of photosensitive elements suited for use in radiography |
US3901711A (en) * | 1972-08-31 | 1975-08-26 | Mitsubishi Paper Mills Ltd | Silver halide photographic emulsion containing a gold salt and a polyalkylene oxide |
US4130429A (en) * | 1972-11-03 | 1978-12-19 | Agfa-Gevaert, N.V. | Combination of photosensitive elements suited for use in radiography |
US3953215A (en) * | 1973-07-16 | 1976-04-27 | Fuji Photo Film Co., Ltd. | Silver halide photographic emulsions |
US4140531A (en) * | 1975-09-10 | 1979-02-20 | Minnesota Mining And Manufacturing Company | Light-handleable photographic materials |
US4180402A (en) * | 1977-11-28 | 1979-12-25 | Vsesojuzny Gosudarstvenny Nauchno-Issiedovatelsky I Proekthyinstitut Khimo-Forograficheskoi Promyshlennosti | Process for obtaining half-tone picture of irregular structure |
US4232116A (en) * | 1979-01-31 | 1980-11-04 | Minnesota Mining And Manufacturing Company | Light-handleable photographic materials |
EP0023661A3 (en) * | 1979-08-02 | 1981-06-03 | Agfa-Gevaert Aktiengesellschaft | Photographic emulsion comprising a stabilizer, preparation process, photographic materials and method of making photographic images |
EP0023661A2 (en) * | 1979-08-02 | 1981-02-11 | Agfa-Gevaert AG | Photographic silver halide emulsion with a stabilizer, process for its production, photographic recording materials and method of making photographic images |
EP0198634A2 (en) | 1985-04-04 | 1986-10-22 | EASTMAN KODAK COMPANY (a New Jersey corporation) | Quaternized tellurium salt fog inhibiting agents for silver halide photography |
US4973548A (en) * | 1988-08-05 | 1990-11-27 | Eastman Kodak Company | Photographic silver bromoiodide emulsions, elements and processes |
US5248577A (en) * | 1990-08-13 | 1993-09-28 | Eastman Kodak Company | Reactant concentration control method and apparatus for precipitation reactions |
EP0616254A1 (en) * | 1993-03-16 | 1994-09-21 | Minnesota Mining And Manufacturing Company | Rapid-access medical x-ray film and process |
US5578411A (en) * | 1993-03-16 | 1996-11-26 | Imation Corp. | Rapid-access medical X-ray film and process |
EP0699944A1 (en) | 1994-08-26 | 1996-03-06 | Eastman Kodak Company | Tabular grain emulsions with sensitization enhancements |
EP0699949A1 (en) | 1994-08-26 | 1996-03-06 | Eastman Kodak Company | Ultrathin tabular grain emulsions with dopants at selected locations |
EP0699950A1 (en) | 1994-08-26 | 1996-03-06 | Eastman Kodak Company | Ultrathin tabular grain emulsions with novel dopant management |
EP1271239A2 (en) | 2001-06-28 | 2003-01-02 | Eastman Kodak Company | Portal imaging assembly with pair of asymmetric screens and method of use |
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