US3218169A - Method of preparing photographic emulsions - Google Patents
Method of preparing photographic emulsions Download PDFInfo
- Publication number
- US3218169A US3218169A US117818A US11781861A US3218169A US 3218169 A US3218169 A US 3218169A US 117818 A US117818 A US 117818A US 11781861 A US11781861 A US 11781861A US 3218169 A US3218169 A US 3218169A
- Authority
- US
- United States
- Prior art keywords
- gelatin
- polymer
- silver halide
- dispersion
- water
- 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
- 238000000034 method Methods 0.000 title claims description 29
- 239000000839 emulsion Substances 0.000 title description 52
- 229920000159 gelatin Polymers 0.000 claims description 54
- 229920000642 polymer Polymers 0.000 claims description 54
- 239000008273 gelatin Substances 0.000 claims description 53
- 229910052709 silver Inorganic materials 0.000 claims description 46
- 239000004332 silver Substances 0.000 claims description 46
- 108010010803 Gelatin Proteins 0.000 claims description 44
- 235000019322 gelatine Nutrition 0.000 claims description 44
- 235000011852 gelatine desserts Nutrition 0.000 claims description 44
- -1 SILVER HALIDE Chemical class 0.000 claims description 39
- 239000006185 dispersion Substances 0.000 claims description 33
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 24
- 229910052739 hydrogen Inorganic materials 0.000 claims description 16
- 239000001257 hydrogen Substances 0.000 claims description 16
- 239000007767 bonding agent Substances 0.000 claims description 13
- 239000002244 precipitate Substances 0.000 claims description 13
- BQCADISMDOOEFD-UHFFFAOYSA-N Silver Chemical compound [Ag] BQCADISMDOOEFD-UHFFFAOYSA-N 0.000 claims description 12
- 239000007864 aqueous solution Substances 0.000 claims description 12
- 239000000084 colloidal system Substances 0.000 claims description 10
- 229920002554 vinyl polymer Polymers 0.000 claims description 10
- 239000000203 mixture Substances 0.000 claims description 8
- 239000007795 chemical reaction product Substances 0.000 claims description 7
- 150000004820 halides Chemical class 0.000 claims description 7
- 239000007788 liquid Substances 0.000 claims description 7
- 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 claims description 7
- 230000001112 coagulating effect Effects 0.000 claims description 5
- 238000002156 mixing Methods 0.000 claims description 5
- 229920003169 water-soluble polymer Polymers 0.000 claims description 5
- 150000001412 amines Chemical class 0.000 claims description 4
- 150000005207 1,3-dihydroxybenzenes Chemical class 0.000 claims description 3
- IZXIZTKNFFYFOF-UHFFFAOYSA-N 2-Oxazolidone Chemical compound O=C1NCCO1 IZXIZTKNFFYFOF-UHFFFAOYSA-N 0.000 claims description 3
- 159000000032 aromatic acids Chemical class 0.000 claims description 3
- 150000002989 phenols Chemical class 0.000 claims description 3
- 150000003000 phloroglucinols Chemical class 0.000 claims description 3
- 238000009877 rendering Methods 0.000 claims description 3
- 150000004893 oxazines Chemical class 0.000 claims description 2
- 229920000036 polyvinylpyrrolidone Polymers 0.000 claims description 2
- 239000000243 solution Substances 0.000 description 17
- 150000003839 salts Chemical class 0.000 description 13
- SQGYOTSLMSWVJD-UHFFFAOYSA-N silver(1+) nitrate Chemical compound [Ag+].[O-]N(=O)=O SQGYOTSLMSWVJD-UHFFFAOYSA-N 0.000 description 12
- NLKNQRATVPKPDG-UHFFFAOYSA-M potassium iodide Inorganic materials [K+].[I-] NLKNQRATVPKPDG-UHFFFAOYSA-M 0.000 description 11
- 238000002360 preparation method Methods 0.000 description 11
- 238000005406 washing Methods 0.000 description 10
- FVAUCKIRQBBSSJ-UHFFFAOYSA-M sodium iodide Chemical compound [Na+].[I-] FVAUCKIRQBBSSJ-UHFFFAOYSA-M 0.000 description 9
- 239000000463 material Substances 0.000 description 8
- 239000000047 product Substances 0.000 description 8
- 239000003795 chemical substances by application Substances 0.000 description 7
- JHJLBTNAGRQEKS-UHFFFAOYSA-M sodium bromide Chemical compound [Na+].[Br-] JHJLBTNAGRQEKS-UHFFFAOYSA-M 0.000 description 7
- 238000013019 agitation Methods 0.000 description 6
- IOLCXVTUBQKXJR-UHFFFAOYSA-M potassium bromide Inorganic materials [K+].[Br-] IOLCXVTUBQKXJR-UHFFFAOYSA-M 0.000 description 6
- 230000008569 process Effects 0.000 description 6
- GHMLBKRAJCXXBS-UHFFFAOYSA-N resorcinol Chemical compound OC1=CC=CC(O)=C1 GHMLBKRAJCXXBS-UHFFFAOYSA-N 0.000 description 6
- 229910001961 silver nitrate Inorganic materials 0.000 description 6
- 239000003518 caustics Substances 0.000 description 5
- IWZKICVEHNUQTL-UHFFFAOYSA-M potassium hydrogen phthalate Chemical compound [K+].OC(=O)C1=CC=CC=C1C([O-])=O IWZKICVEHNUQTL-UHFFFAOYSA-M 0.000 description 5
- 230000005070 ripening Effects 0.000 description 5
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 4
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 4
- 239000008139 complexing agent Substances 0.000 description 4
- 238000001816 cooling Methods 0.000 description 4
- 235000009518 sodium iodide Nutrition 0.000 description 4
- 238000003756 stirring Methods 0.000 description 4
- 239000000126 substance Substances 0.000 description 4
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- WPYMKLBDIGXBTP-UHFFFAOYSA-N benzoic acid Chemical compound OC(=O)C1=CC=CC=C1 WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 description 3
- 239000006227 byproduct Substances 0.000 description 3
- 239000000701 coagulant Substances 0.000 description 3
- 150000001875 compounds Chemical class 0.000 description 3
- 125000000623 heterocyclic group Chemical group 0.000 description 3
- 238000004519 manufacturing process Methods 0.000 description 3
- 238000002844 melting Methods 0.000 description 3
- 230000008018 melting Effects 0.000 description 3
- 235000007715 potassium iodide Nutrition 0.000 description 3
- 230000001681 protective effect Effects 0.000 description 3
- 239000006228 supernatant Substances 0.000 description 3
- AZQWKYJCGOJGHM-UHFFFAOYSA-N 1,4-benzoquinone Chemical compound O=C1C=CC(=O)C=C1 AZQWKYJCGOJGHM-UHFFFAOYSA-N 0.000 description 2
- IMSODMZESSGVBE-UHFFFAOYSA-N 2-Oxazoline Chemical compound C1CN=CO1 IMSODMZESSGVBE-UHFFFAOYSA-N 0.000 description 2
- BCHZICNRHXRCHY-UHFFFAOYSA-N 2h-oxazine Chemical compound N1OC=CC=C1 BCHZICNRHXRCHY-UHFFFAOYSA-N 0.000 description 2
- PAYRUJLWNCNPSJ-UHFFFAOYSA-N Aniline Chemical compound NC1=CC=CC=C1 PAYRUJLWNCNPSJ-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
- KDLHZDBZIXYQEI-UHFFFAOYSA-N Palladium Chemical compound [Pd] KDLHZDBZIXYQEI-UHFFFAOYSA-N 0.000 description 2
- 239000004952 Polyamide Substances 0.000 description 2
- 239000002253 acid Substances 0.000 description 2
- 229910052782 aluminium Inorganic materials 0.000 description 2
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 2
- 239000011248 coating agent Substances 0.000 description 2
- 238000000576 coating method Methods 0.000 description 2
- 238000005189 flocculation Methods 0.000 description 2
- 230000016615 flocculation Effects 0.000 description 2
- LEQAOMBKQFMDFZ-UHFFFAOYSA-N glyoxal Chemical compound O=CC=O LEQAOMBKQFMDFZ-UHFFFAOYSA-N 0.000 description 2
- 150000002343 gold Chemical class 0.000 description 2
- 239000012535 impurity Substances 0.000 description 2
- 230000020477 pH reduction Effects 0.000 description 2
- 239000000123 paper Substances 0.000 description 2
- 239000002245 particle Substances 0.000 description 2
- XNGIFLGASWRNHJ-UHFFFAOYSA-N phthalic acid Chemical compound OC(=O)C1=CC=CC=C1C(O)=O XNGIFLGASWRNHJ-UHFFFAOYSA-N 0.000 description 2
- BASFCYQUMIYNBI-UHFFFAOYSA-N platinum Chemical compound [Pt] BASFCYQUMIYNBI-UHFFFAOYSA-N 0.000 description 2
- 229920002647 polyamide Polymers 0.000 description 2
- 239000011591 potassium Substances 0.000 description 2
- 230000001376 precipitating effect Effects 0.000 description 2
- HNJBEVLQSNELDL-UHFFFAOYSA-N pyrrolidin-2-one Chemical compound O=C1CCCN1 HNJBEVLQSNELDL-UHFFFAOYSA-N 0.000 description 2
- 239000000376 reactant Substances 0.000 description 2
- 239000011734 sodium Substances 0.000 description 2
- NESLWCLHZZISNB-UHFFFAOYSA-M sodium phenolate Chemical compound [Na+].[O-]C1=CC=CC=C1 NESLWCLHZZISNB-UHFFFAOYSA-M 0.000 description 2
- PFNFFQXMRSDOHW-UHFFFAOYSA-N spermine Chemical compound NCCCNCCCCNCCCN PFNFFQXMRSDOHW-UHFFFAOYSA-N 0.000 description 2
- 238000012360 testing method Methods 0.000 description 2
- TXUICONDJPYNPY-UHFFFAOYSA-N (1,10,13-trimethyl-3-oxo-4,5,6,7,8,9,11,12,14,15,16,17-dodecahydrocyclopenta[a]phenanthren-17-yl) heptanoate Chemical compound C1CC2CC(=O)C=C(C)C2(C)C2C1C1CCC(OC(=O)CCCCCC)C1(C)CC2 TXUICONDJPYNPY-UHFFFAOYSA-N 0.000 description 1
- QGKMIGUHVLGJBR-UHFFFAOYSA-M (4z)-1-(3-methylbutyl)-4-[[1-(3-methylbutyl)quinolin-1-ium-4-yl]methylidene]quinoline;iodide Chemical compound [I-].C12=CC=CC=C2N(CCC(C)C)C=CC1=CC1=CC=[N+](CCC(C)C)C2=CC=CC=C12 QGKMIGUHVLGJBR-UHFFFAOYSA-M 0.000 description 1
- LUMLZKVIXLWTCI-NSCUHMNNSA-N (e)-2,3-dichloro-4-oxobut-2-enoic acid Chemical compound OC(=O)C(\Cl)=C(/Cl)C=O LUMLZKVIXLWTCI-NSCUHMNNSA-N 0.000 description 1
- YXIWHUQXZSMYRE-UHFFFAOYSA-N 1,3-benzothiazole-2-thiol Chemical class C1=CC=C2SC(S)=NC2=C1 YXIWHUQXZSMYRE-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
- HXFNRRNDWNSKFM-UHFFFAOYSA-N 3-ethenyl-5-methyl-1,3-oxazolidin-2-one Chemical compound CC1CN(C=C)C(=O)O1 HXFNRRNDWNSKFM-UHFFFAOYSA-N 0.000 description 1
- OCVLSHAVSIYKLI-UHFFFAOYSA-N 3h-1,3-thiazole-2-thione Chemical class SC1=NC=CS1 OCVLSHAVSIYKLI-UHFFFAOYSA-N 0.000 description 1
- UZAAWTQDNCMMEX-UHFFFAOYSA-N 4,4-dimethyl-2-prop-1-en-2-yl-5h-1,3-oxazole Chemical compound CC(=C)C1=NC(C)(C)CO1 UZAAWTQDNCMMEX-UHFFFAOYSA-N 0.000 description 1
- 239000005711 Benzoic acid Substances 0.000 description 1
- ZETHHMPKDUSZQQ-UHFFFAOYSA-N Betulafolienepentol Natural products C1C=C(C)CCC(C(C)CCC=C(C)C)C2C(OC)OC(OC)C2=C1 ZETHHMPKDUSZQQ-UHFFFAOYSA-N 0.000 description 1
- FERIUCNNQQJTOY-UHFFFAOYSA-M Butyrate Chemical compound CCCC([O-])=O FERIUCNNQQJTOY-UHFFFAOYSA-M 0.000 description 1
- FERIUCNNQQJTOY-UHFFFAOYSA-N Butyric acid Natural products CCCC(O)=O FERIUCNNQQJTOY-UHFFFAOYSA-N 0.000 description 1
- 229920008347 Cellulose acetate propionate Polymers 0.000 description 1
- 229920002284 Cellulose triacetate Polymers 0.000 description 1
- 102000008186 Collagen Human genes 0.000 description 1
- 108010035532 Collagen Proteins 0.000 description 1
- RPNUMPOLZDHAAY-UHFFFAOYSA-N Diethylenetriamine Chemical compound NCCNCCN RPNUMPOLZDHAAY-UHFFFAOYSA-N 0.000 description 1
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 1
- 239000005977 Ethylene Substances 0.000 description 1
- 229910002651 NO3 Inorganic materials 0.000 description 1
- NHNBFGGVMKEFGY-UHFFFAOYSA-N Nitrate Chemical compound [O-][N+]([O-])=O NHNBFGGVMKEFGY-UHFFFAOYSA-N 0.000 description 1
- 239000004677 Nylon Substances 0.000 description 1
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 1
- 229920002845 Poly(methacrylic acid) Polymers 0.000 description 1
- 239000002202 Polyethylene glycol Substances 0.000 description 1
- XBDQKXXYIPTUBI-UHFFFAOYSA-M Propionate Chemical compound CCC([O-])=O XBDQKXXYIPTUBI-UHFFFAOYSA-M 0.000 description 1
- KJTLSVCANCCWHF-UHFFFAOYSA-N Ruthenium Chemical compound [Ru] KJTLSVCANCCWHF-UHFFFAOYSA-N 0.000 description 1
- 229910021607 Silver chloride Inorganic materials 0.000 description 1
- 229910021612 Silver iodide Inorganic materials 0.000 description 1
- PCSMJKASWLYICJ-UHFFFAOYSA-N Succinic aldehyde Chemical compound O=CCCC=O PCSMJKASWLYICJ-UHFFFAOYSA-N 0.000 description 1
- 229910021626 Tin(II) chloride Inorganic materials 0.000 description 1
- BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 description 1
- AVMNFQHJOOYCAP-UHFFFAOYSA-N acetic acid;propanoic acid Chemical compound CC(O)=O.CCC(O)=O AVMNFQHJOOYCAP-UHFFFAOYSA-N 0.000 description 1
- 125000002777 acetyl group Chemical class [H]C([H])([H])C(*)=O 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 150000001299 aldehydes Chemical class 0.000 description 1
- 239000003513 alkali Substances 0.000 description 1
- 229910001508 alkali metal halide Inorganic materials 0.000 description 1
- 150000008045 alkali metal halides Chemical class 0.000 description 1
- 235000011126 aluminium potassium sulphate Nutrition 0.000 description 1
- 230000008901 benefit Effects 0.000 description 1
- 235000010233 benzoic acid Nutrition 0.000 description 1
- 239000011230 binding agent Substances 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 229920002678 cellulose Polymers 0.000 description 1
- 239000001913 cellulose Substances 0.000 description 1
- 229920002301 cellulose acetate Polymers 0.000 description 1
- 229920006217 cellulose acetate butyrate Polymers 0.000 description 1
- 229920001727 cellulose butyrate Polymers 0.000 description 1
- 229920006218 cellulose propionate Polymers 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 239000003638 chemical reducing agent Substances 0.000 description 1
- OIDPCXKPHYRNKH-UHFFFAOYSA-J chrome alum Chemical compound [K]OS(=O)(=O)O[Cr]1OS(=O)(=O)O1 OIDPCXKPHYRNKH-UHFFFAOYSA-J 0.000 description 1
- 229920001436 collagen Polymers 0.000 description 1
- 230000000536 complexating effect Effects 0.000 description 1
- 239000013078 crystal Substances 0.000 description 1
- 238000010908 decantation Methods 0.000 description 1
- 238000000354 decomposition reaction Methods 0.000 description 1
- 238000000586 desensitisation Methods 0.000 description 1
- HEOKFDGOFROELJ-UHFFFAOYSA-N diacetal Natural products COc1ccc(C=C/c2cc(O)cc(OC3OC(COC(=O)c4cc(O)c(O)c(O)c4)C(O)C(O)C3O)c2)cc1O HEOKFDGOFROELJ-UHFFFAOYSA-N 0.000 description 1
- 238000009826 distribution Methods 0.000 description 1
- 238000010981 drying operation Methods 0.000 description 1
- 239000000975 dye Substances 0.000 description 1
- 125000004494 ethyl ester group Chemical group 0.000 description 1
- 238000001704 evaporation Methods 0.000 description 1
- 230000008020 evaporation Effects 0.000 description 1
- 239000000499 gel Substances 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 229940015043 glyoxal Drugs 0.000 description 1
- PCHJSUWPFVWCPO-UHFFFAOYSA-N gold Chemical compound [Au] PCHJSUWPFVWCPO-UHFFFAOYSA-N 0.000 description 1
- 229910052737 gold Inorganic materials 0.000 description 1
- 239000010931 gold Substances 0.000 description 1
- 230000008676 import Effects 0.000 description 1
- 238000011065 in-situ storage Methods 0.000 description 1
- 230000005764 inhibitory process Effects 0.000 description 1
- 230000003993 interaction Effects 0.000 description 1
- 150000002500 ions Chemical class 0.000 description 1
- 229910052741 iridium Inorganic materials 0.000 description 1
- GKOZUEZYRPOHIO-UHFFFAOYSA-N iridium atom Chemical compound [Ir] GKOZUEZYRPOHIO-UHFFFAOYSA-N 0.000 description 1
- 150000002576 ketones Chemical class 0.000 description 1
- 239000011159 matrix material Substances 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
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- WSFSSNUMVMOOMR-NJFSPNSNSA-N methanone Chemical compound O=[14CH2] WSFSSNUMVMOOMR-NJFSPNSNSA-N 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- ZAKLKBFCSHJIRI-UHFFFAOYSA-N mucochloric acid Natural products OC1OC(=O)C(Cl)=C1Cl ZAKLKBFCSHJIRI-UHFFFAOYSA-N 0.000 description 1
- 229920001220 nitrocellulos Polymers 0.000 description 1
- 229910000510 noble metal Inorganic materials 0.000 description 1
- 235000012149 noodles Nutrition 0.000 description 1
- 229920001778 nylon Polymers 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 229910052763 palladium Inorganic materials 0.000 description 1
- 230000000737 periodic effect Effects 0.000 description 1
- 229910052697 platinum Inorganic materials 0.000 description 1
- 229920000728 polyester Polymers 0.000 description 1
- 229920001223 polyethylene glycol Polymers 0.000 description 1
- 235000013855 polyvinylpyrrolidone Nutrition 0.000 description 1
- GRLPQNLYRHEGIJ-UHFFFAOYSA-J potassium aluminium sulfate Chemical compound [Al+3].[K+].[O-]S([O-])(=O)=O.[O-]S([O-])(=O)=O GRLPQNLYRHEGIJ-UHFFFAOYSA-J 0.000 description 1
- 239000003755 preservative agent Substances 0.000 description 1
- 125000001453 quaternary ammonium group Chemical group 0.000 description 1
- 230000005855 radiation Effects 0.000 description 1
- 230000009467 reduction Effects 0.000 description 1
- 230000001172 regenerating effect Effects 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- 230000004044 response Effects 0.000 description 1
- 239000000837 restrainer Substances 0.000 description 1
- 229910052703 rhodium Inorganic materials 0.000 description 1
- 239000010948 rhodium Substances 0.000 description 1
- MHOVAHRLVXNVSD-UHFFFAOYSA-N rhodium atom Chemical compound [Rh] MHOVAHRLVXNVSD-UHFFFAOYSA-N 0.000 description 1
- 229910052707 ruthenium Inorganic materials 0.000 description 1
- 230000001235 sensitizing effect Effects 0.000 description 1
- ADZWSOLPGZMUMY-UHFFFAOYSA-M silver bromide Chemical compound [Ag]Br ADZWSOLPGZMUMY-UHFFFAOYSA-M 0.000 description 1
- ZUNKMNLKJXRCDM-UHFFFAOYSA-N silver bromoiodide Chemical compound [Ag].IBr ZUNKMNLKJXRCDM-UHFFFAOYSA-N 0.000 description 1
- 229940045105 silver iodide Drugs 0.000 description 1
- HKZLPVFGJNLROG-UHFFFAOYSA-M silver monochloride Chemical compound [Cl-].[Ag+] HKZLPVFGJNLROG-UHFFFAOYSA-M 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- WXMKPNITSTVMEF-UHFFFAOYSA-M sodium benzoate Chemical compound [Na+].[O-]C(=O)C1=CC=CC=C1 WXMKPNITSTVMEF-UHFFFAOYSA-M 0.000 description 1
- 239000004299 sodium benzoate Substances 0.000 description 1
- 235000010234 sodium benzoate Nutrition 0.000 description 1
- 239000002195 soluble material Substances 0.000 description 1
- 229940063675 spermine Drugs 0.000 description 1
- 239000003381 stabilizer Substances 0.000 description 1
- 239000001119 stannous chloride Substances 0.000 description 1
- 235000011150 stannous chloride Nutrition 0.000 description 1
- 238000003860 storage Methods 0.000 description 1
- 150000003460 sulfonic acids Chemical class 0.000 description 1
- 150000003464 sulfur compounds Chemical class 0.000 description 1
- ILJSQTXMGCGYMG-UHFFFAOYSA-N triacetic acid Chemical compound CC(=O)CC(=O)CC(O)=O ILJSQTXMGCGYMG-UHFFFAOYSA-N 0.000 description 1
- 229920003176 water-insoluble polymer Polymers 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
- G03C1/04—Silver halide emulsions; Preparation thereof; Physical treatment thereof; Incorporation of additives therein with macromolecular additives; with layer-forming substances
Definitions
- This invention relates to photography and, more particularly, to novel photosensitive products and processes for the fabrication of same.
- One object of this invention is to provide novel methods for the fabrication of silver halide photographic emulsions.
- Another object of this invention is to prepare certain specified dispersions of silver halides useful in the preparation of photographic silver halide emulsions.
- Another object of this invention is to provide a novel means of flocking the gelatin in the preparation of photographic silver halide emulsions.
- Another object of this invention is to provide a dispersion of silver halides from which the water-soluble by-products may be readily removed.
- Still another object of the present invention is to provide a method of washing specified silver halide dispersions in which substantially all of the liquid may be removed, thus providing a substantially complete removal of any water-soluble impurities therein.
- the invention accordingly comprises the several steps and the relation and order of one or more such steps with respect to each of the others, and the product possessing the features, properties and the relation of elements which are exemplified in the following detailed disclosure, and the scope of the application of which will be indicated in the claims.
- the most common method of preparing photographic silver halide emulsions is by reacting a water-soluble silver salt, such as silver nitrate, with at least one watersoluble halide, such as potassium or sodium bromide, preferably together with potassium or sodium iodide, in an aqueous solution of a gelatin colloid peptizing agent.
- a water-soluble silver salt such as silver nitrate
- at least one watersoluble halide such as potassium or sodium bromide, preferably together with potassium or sodium iodide
- the dispersion of silver halide thus formed contains water-soluble salts as a by-product of the double decomposition reaction, in addition to an unreacted excess of either of the initial salts. It has been considered desirable in the case of photographic emulsions that the water-soluble salts present in the emulsion be reduced in concentration.
- gelatin has been used as a protective colloid, to remove the soluble material therefrom by setting the gelatin dispersion by means of chilling, noodling the soset dispersion, and washing the noodles with cold Water or
- a gelatin derivative has been employed coagulating the gelatin derivative, separating the coagulant from the supernatant liquor, and washing the separated coagulant with water at such temperature as to keep the coagulant from melting.
- the present invention is concerned with the preparartion of photographic emulsions having silver halide as the sensitive material and wherein the silver halide is prepared and dispersed in an aqueous solution of gelatin.
- a soluble polymer which possesses the property of being insolu'bilized upon complexing with a hydrogen bonding complexant, is added to the dispersion.
- the hydrogen bonding compound is added as a complexing agent.
- Such complexing agents render the polymer insoluble in situ whereby the polymer complex precipitates causing the gelatin to iloc, probably as a co-precipitate due to a physical chain entanglement of the polymer and the gelatin.
- the gelatin and polymercomplexant are then removed from the supernatant liquor and washed with cold water and/ or dilute, cold caustic solution to remove the Water-soluble by-products and other impurities including the polymer and the polymercomplexant.
- the silver halide-gelatin agglomerates may then be formulated into a photographic emulsion by redispersion in a gelatin or the like matrix or vehicle.
- gelatin as utilized herein is intended to signify the art-accepted designation of the photographic colloid binder derived from collagen and comprising a proteinaceaus substance.
- the term is intended to include both acid and alkali process gelatins.
- the silver halide is prepared in an aqueous solution of gelatin as the peptizer.
- the silver halide is preferably prepared by reacting a water-soluble silver salt, preferably silver nitrate, with at least one Water-soluble halide salt, preferably sodium or potassium bromide, most preferably in combination with sodium or potassium iodides, in an aqueous solution of a gelatin colloid peptizing agent.
- a water-soluble polymer capable of being precipitated with hydrogen bonding complexing agents preferably a polyvinyl heterocyclic polymer, e.g., oxazine, oxazoline, oxazolidinone or pyrollidone polymer
- a suitable complexant, Le a hydrogen bonding agent that will precipitate the polymer, e.g., an aromatic acid or aromatic hydroxyl compound, is added, thereby rendering the polymer insoluble and causing the gelatin-silver halide dispersion to fioc, entrapped by the precipitating polymer.
- the flocked material can then be readily separated and washed with water.
- the water-soluble salts and lay-products are thereby readily removed along with the complexed and uncomplexed polymer. Preparation of the emulsion can then be continued in the conventional manner.
- the silver halide crystals may be prepared in the gelatin peptizing agent in any of the normal methods for the preparation of silver halide dispersions, as for example by introducing a stream of an aqueous solution of silver nitrate and a stream of an aqueous solution of at least one alkali-metal halide, preferably potassium or sodium bromide, and potassium or sodium iodide, into a constantly agitated solution of the peptizing agent.
- the gelatin solution may be combined with one of the reactants and the other reactants may be introduced with stirring. After the silver halide has formed, any ripening desirable may be effected.
- the solution is cooled, preferably to a temperature of 30 to 35 C.
- the polymer is then dissolved and thoroughly dispersed in the solution.
- the precipitating polymer carries down the silver halide-gelatin dispersion.
- the coagulum substantially a physical combination of silver halide-gelatin and complexed polymer, uncomplexed polymer and various salts, may then be readily separated from the liquid by any one of several techniques.
- the supernatant liquid may be removed by decantation.
- the coagulum may then be washed by cold Water.
- the coagulum consists of silver halide and gelatin, any other Watersoluble materials which may be present, and a small amount of residual salts dissolved in any water trapped in the coagulum. in addition, a small amount of polymer or polymer complex may be physically trapped by the flocked gelatin.
- the photographic utility of the silver halide-gelatin coagulum has not been deleteriously affected by such a residue. For example, in testing emulsions made by the method of this invention, fog levels were low, no desensitization was apparent, and, when treated with gold sensitizer, good speed response was found.
- the preferred polymer employed in the preparation of the emulsion of this invention is a cold Watersoluble, alkali-soluble, polyvinyl heterocyclic polymer capable of being precipitated by a complexant that is a hydrogen bonding agent.
- such polymers contain a nethyl-2-oxazolidinone ring, e.g., poly-N- vinyl-5-methyl-2-oxazolidinone.
- Polymers of this type are commercially available from the Dow Chemical Com pany, Midland, Michigan, under the trade name Devlex Resins. As an example of such a polymer mention may be made of a polymer of the formula:
- the polymers of the aforementioned type readily complex with hydrogen bonding agents and precipitate quantitatively.
- flocking can be carried out easily and quickly using the process of this invention.
- hydrogen bonding agents used as complexants mention may be made of aromatic hydroxyl compounds such as phenols, resorcinols, phloroglucinols, amines, aromatic acids such as benzoic acid and sulfonic acids, mercaptobenzothiazoles, thiocarbanilides, etc.
- the concentration of complexant necessary to fiocculate is determined on the basis of the particular complexing agent used, but should be at least approximately 2% of the total emulsion on a weight/volume basis, i.e., 2 grams/100 cc. of total emulsion.
- the temperature of the silver halide-gelatin dispersion should preferably be maintained below this point to ensure complete solubility and adequate distribution of the polymer on its addition to the dispersion.
- agitation is continued to provide the necessary interaction between the polymer and complexant. The agitation is then stopped and the fioc allowed to settle. In order to prevent the formation of a gummy mass of gelatin particles, before the agitation is stopped and the fioc allowed to settle, the temperature of the dispersion should be below the melting point of the gelatin.
- the complexant and polymer may be desirable to add at temperatures high enough to provide for thermal agitation of the dispersion with the resulting chain entanglement of the polymer and gelatin and still floc at temperatures below the melting point of the gelatin.
- This may be accomplished by adding the complexant in salt form, e.g., sodium phenate, sodium benzoate or potassium acid phthalate, which does not form an insoluble complex with the polymer, cooling the solution to the desired temperature, and then carrying out the flocculation by regenerating the complexant by acidification whereby it will readily complex with the polymer.
- sodium phenate or potassium acid phthalate will not insolubilize the polymer, but when converted to phenol or phthalic acid by acidification by sulfuric acid, for example, the regenerated complexant will precipitate the polymer.
- the polymer is preferably added to the silver halidegelatin dispersion as a 10% solution in a ratio of 5 to 35 parts of polymer to 10 parts of gelatin. In a preferred embodiment, the ratio is 6 parts of polymer to 10 parts of gelatin, on an air dry Weight basis.
- agitation of the dispersion iscarried on for 2 to 5 minutes. tinuing agitation and cooling. The coagulum then settles and is ready to be separated and washed.
- the precipitated coagulum may be washed with cold water to remove lay-products, excess soluble salts, as well as the polymer and polymer complex. Since the polymer complex is water-insoluble, its removal is accomplished by a stream of cold Water which displaces the polymerpolymer complex equilibrium; It may be desirable, therefore, in order to accelerate the washing process, to precede the cold water wash with an initial caustic wash to remove the Water-insoluble polymer complex.
- polymer complex is intended to signify the reaction product of the polymer and the hydrogen bonding agent complexant.
- this invention provides a novel process for the preparation of photosensitive emulsions that does not involve the use of gelatin derivatives and their attendant disadvantages or any treatment of the gelatin that might interfere with the photographic employment of the emulsion.
- a minimum of steps is necessary in an easy and rapid process that utilizes materials that can be substantially removed from the silver halidegelatin emulsion by a simple wash.
- any small amount of materials remaining entrapped in the emulsion after washing does not interfere with the photographic employment of the emulsion.
- one advantage of the flocculation technique for the preparation of photographic emulsions described herein is that the concentration of silver halide in the final emulsion may be adjusted to any desired value without reference to the quantity of water, silver halide and gelatin employed in the initial reaction for the preparation of the silver halide dispersion.
- concentrated emulsions may be readily prepared.
- Dried emulsions may be prepared for storage and shipment without any necessity of extensive evaporation of water or reduction of the water content of the dispersed silver halide and without the necessity of using concentrated salt solu-
- the complexant is then added with coni tions or organic solvents.
- the coagulum prepared is especially suitable for the preparation of dried emulsions, since it may be obtained in a state nearly free of excess water, and therefore the drying operation is simplified and rendered less expensive.
- the coagulum either prior to or subsequent to restoration of its gel properties, thus may be obtained in a suitable form for this purpose, and the dried coagulum may be readily redispersed at any time.
- Example A To a solution of 230 ml. of water, 34 g. of potassium bromide, 2 g. of potassium iodide and 7 g. of gelatin, maintained at a temperature of 64 C., were added over a one-minute period, 234 ml. of a solution comprising 410 ml. of water and 42 g. of silver nitrate. Another 184 ml. of the silver nitrate solution were added over a 25- minute period. The emulsion was then cooled to 50 C. and ripened for 30 minutes. Ripening was then reduced by cooling the solution to between 30 and 35 C.
- Example I To the emulsion in Example A, there was added, at a temperature of 35 C., 42 ml. of a solution of poly N vinyl-5-methyl-2-oxazolidinone (commercially available from the Dow Chemical Company, Midland, Michigan, under the trade name Devlex 130) and the mixture was stirred for 3 minutes. 180 ml. of 10% potassium acid phthalate solution were then added and stirring continued for 3 minutes. With continued stirring the solution was then cooled below 20 C. The pH was then adjusted to 2.8 with 2 N sulfuric acid. The resulting coagulum was then separated and washed with 1500 ml. of cold water C. or lower) to which had been added 100 ml. of 1 N sodium hydroxide. A cold water wash was then carried out.
- poly N vinyl-5-methyl-2-oxazolidinone commercially available from the Dow Chemical Company, Midland, Michigan, under the trade name Devlex 130
- Example II To 100 ml. of the emulsion prepared as in Example A, there was added, at a temperature of 35 C., 6.5 ml. of a 10% solution of 4,4-dimethyl-2-isopropenyl-oxazoline and the mixture was stirred for 5 minutes. After cooling the emulsion to between 15 and C., ml. of a 10% resorcinol solution were added with stirring. The precipitate was allowed to settle, separated and washed as in Example I.
- the resultant emulsions were sensitized, the desired additives incorporated therein, and the emulsions coated and processed according to conventional procedures known in the emulsion manufacturing art.
- the emulsions of this invention may be coated onto various types of rigid or flexible supports, for example, glass, paper, metal, polymeric films of both the synthetic types and those derived from naturally occurring products, etc.
- suitable materials include paper; aluminum; polymethacrylic acid methyl and ethyl esters; vinyl chloride polymers; polyvinyl acetals; polyamides such as nylon; polyesters such as the polymeric films derived from ethylene glycolterephthalic acid; and cellulose derivatives such as cellulose acetate, triacetate, nitrate, propionate, butyrate, acetate-propionate, or acetatebutyrate.
- the light-sensitive material of the photographic emulsions comprises a compound of silver, for example, one or more of the silver halides of which silver chloride, silver bromide and silver iodide are examples.
- the preferred silver halide emulsion comprises a silver iodobromide emulsion. It will be understood that preferred silver halide emulsions of varying halide concentration may be advantageously employed.
- the emulsions of the present invention may be chemically sensitized by any of the accepted procedures.
- the emulsions may be digested with naturally 6 active gelatin, or sulfur compounds can be added such as those described in US. Patents Nos. 1,574,944, 1,623,- 499 and 2,410,689.
- the emulsions may also be treated with salts of the noble metals such as ruthenium, rhodium, palladium, iridium, and platinum, all of which belong to Group VIII of the Periodic Table of Elements and have an atomic weight greater than 100.
- the salts may be used for sensitizing in amounts below that which produces any substantial fog inhibition, as described in US. Patent No. 2,448,060, and as antifoggants in higher amounts, as described in US. Patents Nos. 2,566,245 and 2,566,- 263.
- the emulsions may also be chemically sensitized with gold salts as described in Us. Patent No. 2,399,083 or stabilized with gold salts as described in US. Patents Nos. 2,597,856 and 2,597,915.
- the emulsions may also be chemically sensitized with reducing agents such as stannous chloride as described in US. Patent No. 2,487,850; amines such as diethylenetriamine as described in US. Patent No. 2,518,698; polyamides such as spermine as described in US. Patent No. 2,521,925; or bis-(fl-aminoethyl)-sulfide and its watersoluble salts as described in US. Patent No. 2,521,926.
- reducing agents such as stannous chloride as described in US. Patent No. 2,487,850; amines such as diethylenetriamine as described in US. Patent No. 2,518,698; polyamides such as spermine as described in US. Patent No. 2,521,925; or bis-(fl-aminoethyl)-sulfide and its watersoluble salts as described in US. Patent No. 2,521,926.
- the emulsions may also be stabilized with the mercury compounds of US. Patents Nos. 2,728,663, 2,728,664 and 2,728,665.
- the emulsions may also be optically sensitized with cyanine and merocyanine dyes as described in U.S. Patents Nos. 1,846,301, 1,846,302, 1,942,854, 1,990,507, 2,112,- 140, 2,165,338, 2,493,747, 2,493,748, 2,503,776, 2,519,- 001, 2,666,761, 2,734,900, 2,739,149 and 2,739,964.
- the emulsions may also contain speed-increasing compounds of the quaternary ammonium type as described in US. Patents Nos. 2,271,623, 2,288,226 and 2,334,864; and of the polyethylene glycol type as described in US. Patent No. 2,708,162.
- suitable antifoggants may be included in the composition of the emulsions.
- Hardening agents such as inorganic agents providing polyvalent metallic atoms, especially polyvalent aluminum or chronium ions, for example, potash alum and chrome alum [K Cr (SO -24H O] and organic agents of the aldehyde type such as formaldehyde, glyoxal, mucochloric acid, etc., the ketone type such as diacetal, and the quinone type, may be incorporated in the emulsions according to procedures well known in the art.
- inorganic agents providing polyvalent metallic atoms especially polyvalent aluminum or chronium ions
- organic agents of the aldehyde type such as formaldehyde, glyoxal, mucochloric acid, etc.
- the ketone type such as diacetal
- quinone type may be incorporated in the emulsions according to procedures well known in the art.
- photosensitive and other terms of similar import are herein employed in the generic sense to describe materials possessing physical and chemical properties which enable them to form usable images when exposed to actinic radiation.
- any residue of polymer that may remain in the silver halide gelatin particles after washing due to physical entrapment does not deleteriously interfere with the photographic employment of the emulsion.
- speed-increasing and fog-depressing characteristics were imparted to test emulsions, by the presence of such polymer.
- a method of preparing silver halide dispersions which comprises the steps of mixing together a watersoluble silver salt and at least one soluble halide in an aqueous solution of a gelatin peptizing colloid, thereby forming a silver halide-gelatin dispersion, adding a watersoluble polymer selected from the group consisting of polyvinyl oxazines, polyvinyl ozazolines, polyvinyl oxazolidinones and polyvinyl pyrrolidones to said silver halide dispersion in gelatin and coagulating the mixture by adding a hydrogen bonding agent selected from the group consisting of phenols, resorcinols, aromatic acids, amines, mercaptothiazoles, phloroglucinols and thiocarbanilides, whereby a water-insoluble reaction product of said water-soluble polymer and said hydrogen bonding agent is formed, separating the resulting percipitate from the liquid portion of the mass, and washing the separated precipitate
- a method as defined in claim 1 wherein said Watersoluble halide is selected from the group consisting of sodium bromide, sodium iodide and potassium iodide.
- polymerto-gelatin ratio is within the range of about 5 to 35 parts of polymer to 10 parts of gelatin.
- a method as defined in claim 1 including the step of mixing said separated precipitate with a polymeric protective colloid for said silver halide gelatin.
- a method as defined in claim 7 including the step of coating said mixture on a support.
- a method of preparing a silver halide dispersion which comprises thesteps of mixing together a watersoluble silver salt and at least one soluble halide in an aqueous solution of a gelatin peptizing colloid, thereby forming a silver halide-gelatin dispersion, adding an aqueous solution of poly-N-vinyl-5-methyl-2-oxazolidinone and potassium acid pht-halate to said silver halide dispersion in gelatin, coagulating the dispersion by acidifying and separating the resulting precipitate from the liquid portion of the mass, and washing said precipitate With an initial caustic wash, followed by a cold water wash, thereby removing substantially all of the reaction product of said poly-N-vinyl-S-methyl-2-oxazolidinone and said potassium acid phthalate.
- a method of preparing a silver halide dispersion which comprises the steps of mixing together a watersoluble silver salt and at least one soluble halide in an aqueous solution of a gelatin peptizing colloid, thereby forming silver halide-gelatin dispersion, adding an aqueous solution of poly-4,4-dimethyl-2-isopropenyl-oxazoline to the silver halide dispersion in gelatin, coagulating by adding resorcinol to said dispersion, separating the resulting precipitate from the liquid portion of the mass, and Washing said precipitate with an initial caustic wash, followed by a cold water wash, thereby removing substantially all of the reaction product of said poly-4,4dimethyl-2- isopropenyl-oxazoline and said resorcinol.
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Description
3,218,169 METHQD F PREPARING PHOTQGRAPHIC EMULSIONS Walter D. Kelly, In, Wellesley Hills, Peter H. Roth, Wa-
tertown, and Lloyd 1). Taylor, Everett, Mass., assignors to Polaroid Corporation, Cambridge, Mass, a corporation of Delaware No Drawing. Filed June 19, 1961, Ser. No. 117,818
11 Claims. (Cl. 96114) This invention relates to photography and, more particularly, to novel photosensitive products and processes for the fabrication of same.
One object of this invention is to provide novel methods for the fabrication of silver halide photographic emulsions.
Another object of this invention is to prepare certain specified dispersions of silver halides useful in the preparation of photographic silver halide emulsions.
Another object of this invention is to provide a novel means of flocking the gelatin in the preparation of photographic silver halide emulsions.
Another object of this invention is to provide a dispersion of silver halides from which the water-soluble by-products may be readily removed.
Still another object of the present invention is to provide a method of washing specified silver halide dispersions in which substantially all of the liquid may be removed, thus providing a substantially complete removal of any water-soluble impurities therein.
Other objects of the invention will in part be obvious and will in part appear hereinafter.
The invention accordingly comprises the several steps and the relation and order of one or more such steps with respect to each of the others, and the product possessing the features, properties and the relation of elements which are exemplified in the following detailed disclosure, and the scope of the application of which will be indicated in the claims.
The most common method of preparing photographic silver halide emulsions is by reacting a water-soluble silver salt, such as silver nitrate, with at least one watersoluble halide, such as potassium or sodium bromide, preferably together with potassium or sodium iodide, in an aqueous solution of a gelatin colloid peptizing agent. The dispersion of silver halide thus formed contains water-soluble salts as a by-product of the double decomposition reaction, in addition to an unreacted excess of either of the initial salts. It has been considered desirable in the case of photographic emulsions that the water-soluble salts present in the emulsion be reduced in concentration. It has generally been the practice, Where gelatin has been used as a protective colloid, to remove the soluble material therefrom by setting the gelatin dispersion by means of chilling, noodling the soset dispersion, and washing the noodles with cold Water or Where a gelatin derivative has been employed coagulating the gelatin derivative, separating the coagulant from the supernatant liquor, and washing the separated coagulant with water at such temperature as to keep the coagulant from melting.
The present invention is concerned with the preparartion of photographic emulsions having silver halide as the sensitive material and wherein the silver halide is prepared and dispersed in an aqueous solution of gelatin. Subsequent to ripening of the emulsion for the desired length of time, a soluble polymer, Which possesses the property of being insolu'bilized upon complexing with a hydrogen bonding complexant, is added to the dispersion. After distributing the polymer throughout the dispersion to ensure sufiicient chain entanglenited States Patent ice ment with the gelatin, the hydrogen bonding compound is added as a complexing agent. Such complexing agents render the polymer insoluble in situ whereby the polymer complex precipitates causing the gelatin to iloc, probably as a co-precipitate due to a physical chain entanglement of the polymer and the gelatin. The gelatin and polymercomplexant are then removed from the supernatant liquor and washed with cold water and/ or dilute, cold caustic solution to remove the Water-soluble by-products and other impurities including the polymer and the polymercomplexant. The silver halide-gelatin agglomerates may then be formulated into a photographic emulsion by redispersion in a gelatin or the like matrix or vehicle.
The term gelatin as utilized herein is intended to signify the art-accepted designation of the photographic colloid binder derived from collagen and comprising a proteinaceaus substance. The term is intended to include both acid and alkali process gelatins.
The term gelatin is also intended to include any other product substantially identical therewith, as for example, where such product is produced synthetically. In carrying out the present invention, the silver halide is prepared in an aqueous solution of gelatin as the peptizer. The silver halide is preferably prepared by reacting a water-soluble silver salt, preferably silver nitrate, with at least one Water-soluble halide salt, preferably sodium or potassium bromide, most preferably in combination with sodium or potassium iodides, in an aqueous solution of a gelatin colloid peptizing agent. Subsequent to ripening for the desired length of time, a water-soluble polymer capable of being precipitated with hydrogen bonding complexing agents, preferably a polyvinyl heterocyclic polymer, e.g., oxazine, oxazoline, oxazolidinone or pyrollidone polymer, is dispersed in the solution. A suitable complexant, Le, a hydrogen bonding agent that will precipitate the polymer, e.g., an aromatic acid or aromatic hydroxyl compound, is added, thereby rendering the polymer insoluble and causing the gelatin-silver halide dispersion to fioc, entrapped by the precipitating polymer. The flocked material can then be readily separated and washed with water. The water-soluble salts and lay-products are thereby readily removed along with the complexed and uncomplexed polymer. Preparation of the emulsion can then be continued in the conventional manner.
The silver halide crystals may be prepared in the gelatin peptizing agent in any of the normal methods for the preparation of silver halide dispersions, as for example by introducing a stream of an aqueous solution of silver nitrate and a stream of an aqueous solution of at least one alkali-metal halide, preferably potassium or sodium bromide, and potassium or sodium iodide, into a constantly agitated solution of the peptizing agent. Alternatively, the gelatin solution may be combined with one of the reactants and the other reactants may be introduced with stirring. After the silver halide has formed, any ripening desirable may be effected. Subsequent to ripening, the solution is cooled, preferably to a temperature of 30 to 35 C. The polymer is then dissolved and thoroughly dispersed in the solution. Upon addition of the complexant, the precipitating polymer carries down the silver halide-gelatin dispersion. The coagulum, substantially a physical combination of silver halide-gelatin and complexed polymer, uncomplexed polymer and various salts, may then be readily separated from the liquid by any one of several techniques.
In simplest form, the supernatant liquid may be removed by decantation. The coagulum may then be washed by cold Water. After washing, the coagulum consists of silver halide and gelatin, any other Watersoluble materials which may be present, and a small amount of residual salts dissolved in any water trapped in the coagulum. in addition, a small amount of polymer or polymer complex may be physically trapped by the flocked gelatin. However, it has been found that the photographic utility of the silver halide-gelatin coagulum has not been deleteriously affected by such a residue. For example, in testing emulsions made by the method of this invention, fog levels were low, no desensitization was apparent, and, when treated with gold sensitizer, good speed response was found.
The preferred polymer employed in the preparation of the emulsion of this invention is a cold Watersoluble, alkali-soluble, polyvinyl heterocyclic polymer capable of being precipitated by a complexant that is a hydrogen bonding agent. In a preferred embodiment, such polymers contain a nethyl-2-oxazolidinone ring, e.g., poly-N- vinyl-5-methyl-2-oxazolidinone. Polymers of this type are commercially available from the Dow Chemical Com pany, Midland, Michigan, under the trade name Devlex Resins. As an example of such a polymer mention may be made of a polymer of the formula:
1 *i --CHCH s: (E \C=O As examples of other suitable polyvinyl heterocyclic polymers useful in this invention mention may be made of oxazine, oxazoline and pyrrolidone polymers, for example, polymers of the formulae:
I on-om The polymers of Formulae 2 and 3 are disclosed in US. Patent No. 2,897,182, issued July 28, 1959. Polymers of Formula 4 are commercially available from General Aniline and Film Corp, Binghamton, New York.
The polymers of the aforementioned type readily complex with hydrogen bonding agents and precipitate quantitatively. Thus, flocking can be carried out easily and quickly using the process of this invention. As examples of hydrogen bonding agents used as complexants, mention may be made of aromatic hydroxyl compounds such as phenols, resorcinols, phloroglucinols, amines, aromatic acids such as benzoic acid and sulfonic acids, mercaptobenzothiazoles, thiocarbanilides, etc. The concentration of complexant necessary to fiocculate is determined on the basis of the particular complexing agent used, but should be at least approximately 2% of the total emulsion on a weight/volume basis, i.e., 2 grams/100 cc. of total emulsion.
Since the polymers suitable for use in this invention are very soluble in cold water and generally become increasingly insoluble in water above 40 C., the temperature of the silver halide-gelatin dispersion should preferably be maintained below this point to ensure complete solubility and adequate distribution of the polymer on its addition to the dispersion. After the addition of the complexant to the dispersion, agitation is continued to provide the necessary interaction between the polymer and complexant. The agitation is then stopped and the fioc allowed to settle. In order to prevent the formation of a gummy mass of gelatin particles, before the agitation is stopped and the fioc allowed to settle, the temperature of the dispersion should be below the melting point of the gelatin.
In the preparation of some emulsions it may be desirable to add the complexant and polymer at temperatures high enough to provide for thermal agitation of the dispersion with the resulting chain entanglement of the polymer and gelatin and still floc at temperatures below the melting point of the gelatin. This may be accomplished by adding the complexant in salt form, e.g., sodium phenate, sodium benzoate or potassium acid phthalate, which does not form an insoluble complex with the polymer, cooling the solution to the desired temperature, and then carrying out the flocculation by regenerating the complexant by acidification whereby it will readily complex with the polymer. For example, sodium phenate or potassium acid phthalate will not insolubilize the polymer, but when converted to phenol or phthalic acid by acidification by sulfuric acid, for example, the regenerated complexant will precipitate the polymer.
The polymer is preferably added to the silver halidegelatin dispersion as a 10% solution in a ratio of 5 to 35 parts of polymer to 10 parts of gelatin. In a preferred embodiment, the ratio is 6 parts of polymer to 10 parts of gelatin, on an air dry Weight basis. After addition of the polymer, agitation of the dispersion iscarried on for 2 to 5 minutes. tinuing agitation and cooling. The coagulum then settles and is ready to be separated and washed.
As described above the precipitated coagulum may be washed with cold water to remove lay-products, excess soluble salts, as well as the polymer and polymer complex. Since the polymer complex is water-insoluble, its removal is accomplished by a stream of cold Water which displaces the polymerpolymer complex equilibrium; It may be desirable, therefore, in order to accelerate the washing process, to precede the cold water wash with an initial caustic wash to remove the Water-insoluble polymer complex.
As used herein, the term polymer complex is intended to signify the reaction product of the polymer and the hydrogen bonding agent complexant.
It can be readily seen that this invention provides a novel process for the preparation of photosensitive emulsions that does not involve the use of gelatin derivatives and their attendant disadvantages or any treatment of the gelatin that might interfere with the photographic employment of the emulsion. A minimum of steps is necessary in an easy and rapid process that utilizes materials that can be substantially removed from the silver halidegelatin emulsion by a simple wash. In addition, any small amount of materials remaining entrapped in the emulsion after washing does not interfere with the photographic employment of the emulsion.
It is apparent that one advantage of the flocculation technique for the preparation of photographic emulsions described herein is that the concentration of silver halide in the final emulsion may be adjusted to any desired value without reference to the quantity of water, silver halide and gelatin employed in the initial reaction for the preparation of the silver halide dispersion. Thus, concentrated emulsions may be readily prepared. Dried emulsions may be prepared for storage and shipment without any necessity of extensive evaporation of water or reduction of the water content of the dispersed silver halide and without the necessity of using concentrated salt solu- The complexant is then added with coni tions or organic solvents. The coagulum prepared is especially suitable for the preparation of dried emulsions, since it may be obtained in a state nearly free of excess water, and therefore the drying operation is simplified and rendered less expensive. The coagulum, either prior to or subsequent to restoration of its gel properties, thus may be obtained in a suitable form for this purpose, and the dried coagulum may be readily redispersed at any time.
The following non-limiting examples illustrate the preparation of the emulsions within this invention.
Example A To a solution of 230 ml. of water, 34 g. of potassium bromide, 2 g. of potassium iodide and 7 g. of gelatin, maintained at a temperature of 64 C., were added over a one-minute period, 234 ml. of a solution comprising 410 ml. of water and 42 g. of silver nitrate. Another 184 ml. of the silver nitrate solution were added over a 25- minute period. The emulsion was then cooled to 50 C. and ripened for 30 minutes. Ripening was then reduced by cooling the solution to between 30 and 35 C.
Example I To the emulsion in Example A, there was added, at a temperature of 35 C., 42 ml. of a solution of poly N vinyl-5-methyl-2-oxazolidinone (commercially available from the Dow Chemical Company, Midland, Michigan, under the trade name Devlex 130) and the mixture was stirred for 3 minutes. 180 ml. of 10% potassium acid phthalate solution were then added and stirring continued for 3 minutes. With continued stirring the solution was then cooled below 20 C. The pH was then adjusted to 2.8 with 2 N sulfuric acid. The resulting coagulum was then separated and washed with 1500 ml. of cold water C. or lower) to which had been added 100 ml. of 1 N sodium hydroxide. A cold water wash was then carried out.
Example II To 100 ml. of the emulsion prepared as in Example A, there was added, at a temperature of 35 C., 6.5 ml. of a 10% solution of 4,4-dimethyl-2-isopropenyl-oxazoline and the mixture was stirred for 5 minutes. After cooling the emulsion to between 15 and C., ml. of a 10% resorcinol solution were added with stirring. The precipitate was allowed to settle, separated and washed as in Example I.
The resultant emulsions were sensitized, the desired additives incorporated therein, and the emulsions coated and processed according to conventional procedures known in the emulsion manufacturing art.
The emulsions of this invention may be coated onto various types of rigid or flexible supports, for example, glass, paper, metal, polymeric films of both the synthetic types and those derived from naturally occurring products, etc. Especially suitable materials include paper; aluminum; polymethacrylic acid methyl and ethyl esters; vinyl chloride polymers; polyvinyl acetals; polyamides such as nylon; polyesters such as the polymeric films derived from ethylene glycolterephthalic acid; and cellulose derivatives such as cellulose acetate, triacetate, nitrate, propionate, butyrate, acetate-propionate, or acetatebutyrate.
The light-sensitive material of the photographic emulsions comprises a compound of silver, for example, one or more of the silver halides of which silver chloride, silver bromide and silver iodide are examples. The preferred silver halide emulsion comprises a silver iodobromide emulsion. It will be understood that preferred silver halide emulsions of varying halide concentration may be advantageously employed.
The emulsions of the present invention may be chemically sensitized by any of the accepted procedures. For example, the emulsions may be digested with naturally 6 active gelatin, or sulfur compounds can be added such as those described in US. Patents Nos. 1,574,944, 1,623,- 499 and 2,410,689.
The emulsions may also be treated with salts of the noble metals such as ruthenium, rhodium, palladium, iridium, and platinum, all of which belong to Group VIII of the Periodic Table of Elements and have an atomic weight greater than 100. The salts may be used for sensitizing in amounts below that which produces any substantial fog inhibition, as described in US. Patent No. 2,448,060, and as antifoggants in higher amounts, as described in US. Patents Nos. 2,566,245 and 2,566,- 263.
The emulsions may also be chemically sensitized with gold salts as described in Us. Patent No. 2,399,083 or stabilized with gold salts as described in US. Patents Nos. 2,597,856 and 2,597,915.
The emulsions may also be chemically sensitized with reducing agents such as stannous chloride as described in US. Patent No. 2,487,850; amines such as diethylenetriamine as described in US. Patent No. 2,518,698; polyamides such as spermine as described in US. Patent No. 2,521,925; or bis-(fl-aminoethyl)-sulfide and its watersoluble salts as described in US. Patent No. 2,521,926.
The emulsions may also be stabilized with the mercury compounds of US. Patents Nos. 2,728,663, 2,728,664 and 2,728,665.
The emulsions may also be optically sensitized with cyanine and merocyanine dyes as described in U.S. Patents Nos. 1,846,301, 1,846,302, 1,942,854, 1,990,507, 2,112,- 140, 2,165,338, 2,493,747, 2,493,748, 2,503,776, 2,519,- 001, 2,666,761, 2,734,900, 2,739,149 and 2,739,964.
The emulsions may also contain speed-increasing compounds of the quaternary ammonium type as described in US. Patents Nos. 2,271,623, 2,288,226 and 2,334,864; and of the polyethylene glycol type as described in US. Patent No. 2,708,162.
Where desired, suitable antifoggants, restrainers, accelerators, preservatives, coating aids, and/or stabilizers may be included in the composition of the emulsions.
Hardening agents such as inorganic agents providing polyvalent metallic atoms, especially polyvalent aluminum or chronium ions, for example, potash alum and chrome alum [K Cr (SO -24H O] and organic agents of the aldehyde type such as formaldehyde, glyoxal, mucochloric acid, etc., the ketone type such as diacetal, and the quinone type, may be incorporated in the emulsions according to procedures well known in the art.
The term photosensitive and other terms of similar import are herein employed in the generic sense to describe materials possessing physical and chemical properties which enable them to form usable images when exposed to actinic radiation.
It has been stated above that any residue of polymer that may remain in the silver halide gelatin particles after washing due to physical entrapment does not deleteriously interfere with the photographic employment of the emulsion. In fact, speed-increasing and fog-depressing characteristics were imparted to test emulsions, by the presence of such polymer.
Since certain changes may be made in the above process and product without departing from the scope of the invention herein involved, it is intended that all matter contained in the above description shall be interpreted as illustrative and not in a limiting sense.
What is claimed is:
1. A method of preparing silver halide dispersions which comprises the steps of mixing together a watersoluble silver salt and at least one soluble halide in an aqueous solution of a gelatin peptizing colloid, thereby forming a silver halide-gelatin dispersion, adding a watersoluble polymer selected from the group consisting of polyvinyl oxazines, polyvinyl ozazolines, polyvinyl oxazolidinones and polyvinyl pyrrolidones to said silver halide dispersion in gelatin and coagulating the mixture by adding a hydrogen bonding agent selected from the group consisting of phenols, resorcinols, aromatic acids, amines, mercaptothiazoles, phloroglucinols and thiocarbanilides, whereby a water-insoluble reaction product of said water-soluble polymer and said hydrogen bonding agent is formed, separating the resulting percipitate from the liquid portion of the mass, and washing the separated precipitate with a cold water wash, thereby rendering it substantially free of said reaction product of said polymer and said hydrogen bonding agent.
2. A method as described in claim 1 wherein said water-soluble silver salt comprises silver nitrate.
3. A method as defined in claim 1 wherein said Watersoluble halide is selected from the group consisting of sodium bromide, sodium iodide and potassium iodide.
4. A method as defined in claim 1 wherein the polymerto-gelatin ratio is within the range of about 5 to 35 parts of polymer to 10 parts of gelatin.
5. A method as defined in claim 1 wherein said cold water wash is immediately preceded by a caustic wash.
6. A method as defined in claim 1 wherein said hydrogen bonding agent is added to said mixture as a salt thereof and free hydrogen bonding agent is provided by acidifying said mixture.
7. A method as defined in claim 1 including the step of mixing said separated precipitate with a polymeric protective colloid for said silver halide gelatin.
8. A method as defined in claim 7 including the step of coating said mixture on a support.
9. A method as defined in claim 7 wherein said polymeric protective colloid comprises gelatin.
10. A method of preparing a silver halide dispersion Which comprises thesteps of mixing together a watersoluble silver salt and at least one soluble halide in an aqueous solution of a gelatin peptizing colloid, thereby forming a silver halide-gelatin dispersion, adding an aqueous solution of poly-N-vinyl-5-methyl-2-oxazolidinone and potassium acid pht-halate to said silver halide dispersion in gelatin, coagulating the dispersion by acidifying and separating the resulting precipitate from the liquid portion of the mass, and washing said precipitate With an initial caustic wash, followed by a cold water wash, thereby removing substantially all of the reaction product of said poly-N-vinyl-S-methyl-2-oxazolidinone and said potassium acid phthalate.
11. A method of preparing a silver halide dispersion which comprises the steps of mixing together a watersoluble silver salt and at least one soluble halide in an aqueous solution of a gelatin peptizing colloid, thereby forming silver halide-gelatin dispersion, adding an aqueous solution of poly-4,4-dimethyl-2-isopropenyl-oxazoline to the silver halide dispersion in gelatin, coagulating by adding resorcinol to said dispersion, separating the resulting precipitate from the liquid portion of the mass, and Washing said precipitate with an initial caustic wash, followed by a cold water wash, thereby removing substantially all of the reaction product of said poly-4,4dimethyl-2- isopropenyl-oxazoline and said resorcinol.
References Cited by the Examiner UNITED STATES PATENTS 1/1950 Bolton 96-94 7/1962 Forsgard 96-114 OTHER REFERENCES NORMAN G. TORCHIN, Primary Examiner.
HAROLD N. BURNSTEIN, Examiner.
Claims (1)
1. A METHOD OF PREPARING SILVER HALIDE DISPERSIONS WHICH COMPRISES THE STEPS OF MIXING TOGETHER A WATERSOLUBLE SILVER SALT AND AT LEASST ONE SOLUBLE HALIDE IN AN AQUEOUS SOLUTION OF A GELATIN PEPTIZING COLLOID, THEREBY FORMING A SILVER HALIDE-GELATIN DISPERSION, ADDIDDNG A WATERSOLUBLE POLYMER SELECTED FROM THE GROUP CONSISTING OF POLYVINYL OXAZINES, POLYVINYL OZAZOLINES, POLYVINYL OXAZOLIDINONES AND POLYVINYL PYRROLIDONES TO SAID SILVER HALIDE DISPERSION IN GELATIN AND COAGULATING THE MIXTURE BY ADDING A HYDROGEN BONDING AGENT SELECTED FROM THE GROUP CONSISTING OF PHENOLS, RESORCINOLS, AROMATIC ACIDS, AMINES, MERCAPTOTHIAZOLES, PHLOROGLUCINOLS AND THIOCARBANILIDES, WHEREBY A WATER-INSOLUBLE REACTION PRODUCT OF SAID WATER-SOLUBLE POLYMER AND SAID HYDROGEN BONDING AGENT IS FORMED, SEPARATING THE RESULTING PERCIPITATE FROM THE LIQUID PORTION OF THE MASS, AND WASHING THE SEPARATED PRECIPITATE WITH A COLD WATER WASH, THEREBY RENDERING IT SUBSTANTIALLY FREE OF SAID REACTION PRODUCT OF SAID POLYMER AND SAID HYDROGEN BONDING AGENT.
Priority Applications (4)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US117818A US3218169A (en) | 1961-06-19 | 1961-06-19 | Method of preparing photographic emulsions |
GB22720/62A GB981251A (en) | 1961-06-19 | 1962-06-13 | Process for preparing a silver halide-gelatin coagulum |
FR900758A FR1331614A (en) | 1961-06-19 | 1962-06-14 | Process for preparing emulsions used in photography |
BE619075A BE619075A (en) | 1961-06-19 | 1962-06-18 | Process for preparing emulsions used in photography. |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US117818A US3218169A (en) | 1961-06-19 | 1961-06-19 | Method of preparing photographic emulsions |
Publications (1)
Publication Number | Publication Date |
---|---|
US3218169A true US3218169A (en) | 1965-11-16 |
Family
ID=22374993
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US117818A Expired - Lifetime US3218169A (en) | 1961-06-19 | 1961-06-19 | Method of preparing photographic emulsions |
Country Status (3)
Country | Link |
---|---|
US (1) | US3218169A (en) |
BE (1) | BE619075A (en) |
GB (1) | GB981251A (en) |
Cited By (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3367777A (en) * | 1964-01-14 | 1968-02-06 | Gen Aniline & Film Corp | Prevention of silver occlusion in color photography |
US3518086A (en) * | 1967-04-18 | 1970-06-30 | Gaf Corp | Silver halide emulsions for lithography |
US3522053A (en) * | 1965-02-06 | 1970-07-28 | Fuji Photo Film Co Ltd | Process for the preparation of photographic emulsions |
US6048906A (en) * | 1997-01-10 | 2000-04-11 | Agfa Gevaert N.V. | Preparation of finely-divided, homodisperse suspensions |
WO2013001096A1 (en) | 2011-06-30 | 2013-01-03 | Dsm Ip Assets B.V. | Silicone-containing monomer |
Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2495918A (en) * | 1948-08-28 | 1950-01-31 | Du Pont | Poly-n-vinyl lactam photographic silver halide emulsions |
US3043697A (en) * | 1958-08-27 | 1962-07-10 | Du Pont | Photographic gelatin-n-vinyllactam silver halide emulsions containing phenolic antifoggants |
-
1961
- 1961-06-19 US US117818A patent/US3218169A/en not_active Expired - Lifetime
-
1962
- 1962-06-13 GB GB22720/62A patent/GB981251A/en not_active Expired
- 1962-06-18 BE BE619075A patent/BE619075A/en unknown
Patent Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2495918A (en) * | 1948-08-28 | 1950-01-31 | Du Pont | Poly-n-vinyl lactam photographic silver halide emulsions |
US3043697A (en) * | 1958-08-27 | 1962-07-10 | Du Pont | Photographic gelatin-n-vinyllactam silver halide emulsions containing phenolic antifoggants |
Cited By (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3367777A (en) * | 1964-01-14 | 1968-02-06 | Gen Aniline & Film Corp | Prevention of silver occlusion in color photography |
US3522053A (en) * | 1965-02-06 | 1970-07-28 | Fuji Photo Film Co Ltd | Process for the preparation of photographic emulsions |
US3518086A (en) * | 1967-04-18 | 1970-06-30 | Gaf Corp | Silver halide emulsions for lithography |
US6048906A (en) * | 1997-01-10 | 2000-04-11 | Agfa Gevaert N.V. | Preparation of finely-divided, homodisperse suspensions |
WO2013001096A1 (en) | 2011-06-30 | 2013-01-03 | Dsm Ip Assets B.V. | Silicone-containing monomer |
Also Published As
Publication number | Publication date |
---|---|
BE619075A (en) | 1962-12-18 |
GB981251A (en) | 1965-01-20 |
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