GB558710A - Improvements in and relating to sensitive photographic materials - Google Patents
Improvements in and relating to sensitive photographic materialsInfo
- Publication number
- GB558710A GB558710A GB271/42A GB27142A GB558710A GB 558710 A GB558710 A GB 558710A GB 271/42 A GB271/42 A GB 271/42A GB 27142 A GB27142 A GB 27142A GB 558710 A GB558710 A GB 558710A
- Authority
- GB
- United Kingdom
- Prior art keywords
- prepared
- bis
- perchlorate
- toluenesulphonate
- ethylene
- 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
Links
- 239000000463 material Substances 0.000 title abstract 2
- VLTRZXGMWDSKGL-UHFFFAOYSA-M perchlorate Inorganic materials [O-]Cl(=O)(=O)=O VLTRZXGMWDSKGL-UHFFFAOYSA-M 0.000 abstract 17
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 abstract 15
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 abstract 15
- 238000010438 heat treatment Methods 0.000 abstract 15
- VLTRZXGMWDSKGL-UHFFFAOYSA-N perchloric acid Chemical compound OCl(=O)(=O)=O VLTRZXGMWDSKGL-UHFFFAOYSA-N 0.000 abstract 15
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 abstract 9
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 abstract 9
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 abstract 8
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 abstract 7
- 239000005977 Ethylene Substances 0.000 abstract 7
- -1 silver halide Chemical class 0.000 abstract 7
- VUQUOGPMUUJORT-UHFFFAOYSA-N methyl 4-methylbenzenesulfonate Chemical compound COS(=O)(=O)C1=CC=C(C)C=C1 VUQUOGPMUUJORT-UHFFFAOYSA-N 0.000 abstract 6
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 abstract 5
- 238000010992 reflux Methods 0.000 abstract 5
- GTQHJCOHNAFHRE-UHFFFAOYSA-N 1,10-dibromodecane Chemical compound BrCCCCCCCCCCBr GTQHJCOHNAFHRE-UHFFFAOYSA-N 0.000 abstract 4
- BSKHPKMHTQYZBB-UHFFFAOYSA-N 2-methylpyridine Chemical compound CC1=CC=CC=N1 BSKHPKMHTQYZBB-UHFFFAOYSA-N 0.000 abstract 4
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 abstract 4
- 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 abstract 4
- WNAHIZMDSQCWRP-UHFFFAOYSA-N dodecane-1-thiol Chemical compound CCCCCCCCCCCCS WNAHIZMDSQCWRP-UHFFFAOYSA-N 0.000 abstract 4
- 150000004714 phosphonium salts Chemical class 0.000 abstract 4
- 150000003839 salts Chemical class 0.000 abstract 4
- 229910052708 sodium Inorganic materials 0.000 abstract 4
- 239000011734 sodium Substances 0.000 abstract 4
- HLHLVGDUYHHOQC-UHFFFAOYSA-N 1-(chloromethylsulfanyl)nonane Chemical compound C(CCCCCCCC)SCCl HLHLVGDUYHHOQC-UHFFFAOYSA-N 0.000 abstract 3
- XKTYXVDYIKIYJP-UHFFFAOYSA-N 3h-dioxole Chemical compound C1OOC=C1 XKTYXVDYIKIYJP-UHFFFAOYSA-N 0.000 abstract 3
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 abstract 3
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 abstract 3
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 abstract 3
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 abstract 3
- RWSOTUBLDIXVET-UHFFFAOYSA-O sulfonium Chemical compound [SH3+] RWSOTUBLDIXVET-UHFFFAOYSA-O 0.000 abstract 3
- BGJSXRVXTHVRSN-UHFFFAOYSA-N 1,3,5-trioxane Chemical group C1OCOCO1 BGJSXRVXTHVRSN-UHFFFAOYSA-N 0.000 abstract 2
- PAMIQIKDUOTOBW-UHFFFAOYSA-N 1-methylpiperidine Chemical compound CN1CCCCC1 PAMIQIKDUOTOBW-UHFFFAOYSA-N 0.000 abstract 2
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 abstract 2
- WTJNKEIBDJTBNP-UHFFFAOYSA-N C1(=CC=C(C=C1)S(=O)(=O)[O-])C.C(CCCCCCCCCCC)C[SH2+] Chemical compound C1(=CC=C(C=C1)S(=O)(=O)[O-])C.C(CCCCCCCCCCC)C[SH2+] WTJNKEIBDJTBNP-UHFFFAOYSA-N 0.000 abstract 2
- SRUXSLLKUMVACM-UHFFFAOYSA-N C1(=CC=C(C=C1)S(=O)(=O)[O-])C.C[SH+]CCCCCCCCC Chemical compound C1(=CC=C(C=C1)S(=O)(=O)[O-])C.C[SH+]CCCCCCCCC SRUXSLLKUMVACM-UHFFFAOYSA-N 0.000 abstract 2
- AFLZFDFEEJQDFX-UHFFFAOYSA-N N-ethyl-N-(nonylsulfanylmethyl)ethanamine Chemical compound C(C)N(CSCCCCCCCCC)CC AFLZFDFEEJQDFX-UHFFFAOYSA-N 0.000 abstract 2
- 150000001875 compounds Chemical class 0.000 abstract 2
- JQVDAXLFBXTEQA-UHFFFAOYSA-N dibutylamine Chemical compound CCCCNCCCC JQVDAXLFBXTEQA-UHFFFAOYSA-N 0.000 abstract 2
- XXBDWLFCJWSEKW-UHFFFAOYSA-N dimethylbenzylamine Chemical compound CN(C)CC1=CC=CC=C1 XXBDWLFCJWSEKW-UHFFFAOYSA-N 0.000 abstract 2
- 235000019441 ethanol Nutrition 0.000 abstract 2
- XYFCBTPGUUZFHI-UHFFFAOYSA-N phosphine group Chemical group P XYFCBTPGUUZFHI-UHFFFAOYSA-N 0.000 abstract 2
- 125000001453 quaternary ammonium group Chemical group 0.000 abstract 2
- 150000003242 quaternary ammonium salts Chemical class 0.000 abstract 2
- 150000003512 tertiary amines Chemical class 0.000 abstract 2
- RXJKFRMDXUJTEX-UHFFFAOYSA-N triethylphosphine Chemical compound CCP(CC)CC RXJKFRMDXUJTEX-UHFFFAOYSA-N 0.000 abstract 2
- 238000010792 warming Methods 0.000 abstract 2
- ZBXKJRQZMCTEQZ-UHFFFAOYSA-N 1,1-bis(nonylsulfanylmethylsulfanyl)decane Chemical compound C(CCCCCCCC)SCSC(CCCCCCCCC)SCSCCCCCCCCC ZBXKJRQZMCTEQZ-UHFFFAOYSA-N 0.000 abstract 1
- PAAZPARNPHGIKF-UHFFFAOYSA-N 1,2-dibromoethane Chemical compound BrCCBr PAAZPARNPHGIKF-UHFFFAOYSA-N 0.000 abstract 1
- HXUJKRYVDADXPR-UHFFFAOYSA-N 1,2-dichloro-4-(3,4-dichlorobutoxy)butane Chemical compound ClCC(Cl)CCOCCC(Cl)CCl HXUJKRYVDADXPR-UHFFFAOYSA-N 0.000 abstract 1
- VEFLKXRACNJHOV-UHFFFAOYSA-N 1,3-dibromopropane Chemical compound BrCCCBr VEFLKXRACNJHOV-UHFFFAOYSA-N 0.000 abstract 1
- ZXBDFBWCRWBMOP-UHFFFAOYSA-N 1,4-bis(nonylsulfanylmethyl)benzene Chemical compound C(CCCCCCCC)SCC1=CC=C(C=C1)CSCCCCCCCCC ZXBDFBWCRWBMOP-UHFFFAOYSA-N 0.000 abstract 1
- ULTHEAFYOOPTTB-UHFFFAOYSA-N 1,4-dibromobutane Chemical compound BrCCCCBr ULTHEAFYOOPTTB-UHFFFAOYSA-N 0.000 abstract 1
- GZEIRSGJNSRLGQ-UHFFFAOYSA-N 1,4-dichloro-1-(1,4-dichlorobutoxy)butane Chemical compound ClCCCC(Cl)OC(CCCCl)Cl GZEIRSGJNSRLGQ-UHFFFAOYSA-N 0.000 abstract 1
- APEXSWAVQWVHTI-UHFFFAOYSA-N 1-(5-methyl-1-phenyl-1H-pyrazol-1-ium-4-yl)ethanone perchlorate Chemical compound Cl(=O)(=O)(=O)[O-].C1(=CC=CC=C1)[NH+]1N=CC(=C1C)C(C)=O APEXSWAVQWVHTI-UHFFFAOYSA-N 0.000 abstract 1
- FZEDJUVQMGBVRC-UHFFFAOYSA-N 1-(5-methyl-1-phenylpyrazol-4-yl)ethanone Chemical compound CC1=C(C(=O)C)C=NN1C1=CC=CC=C1 FZEDJUVQMGBVRC-UHFFFAOYSA-N 0.000 abstract 1
- XFIOOAZXKCGTTG-UHFFFAOYSA-N 1-[2-(dodecylsulfanylmethoxy)ethoxymethylsulfanyl]dodecane Chemical compound C(COCSCCCCCCCCCCCC)OCSCCCCCCCCCCCC XFIOOAZXKCGTTG-UHFFFAOYSA-N 0.000 abstract 1
- CNDHHGUSRIZDSL-UHFFFAOYSA-N 1-chlorooctane Chemical compound CCCCCCCCCl CNDHHGUSRIZDSL-UHFFFAOYSA-N 0.000 abstract 1
- GXWIEXDPIRBOGG-UHFFFAOYSA-M 1-ethylpyridin-1-ium;perchlorate Chemical compound [O-]Cl(=O)(=O)=O.CC[N+]1=CC=CC=C1 GXWIEXDPIRBOGG-UHFFFAOYSA-M 0.000 abstract 1
- GXSAYTBMJSREAH-UHFFFAOYSA-M 1-methylpyridin-1-ium;perchlorate Chemical compound [O-]Cl(=O)(=O)=O.C[N+]1=CC=CC=C1 GXSAYTBMJSREAH-UHFFFAOYSA-M 0.000 abstract 1
- PLZKUGNPZXCRBY-UHFFFAOYSA-N 1-nonylpyridin-1-ium Chemical compound CCCCCCCCC[N+]1=CC=CC=C1 PLZKUGNPZXCRBY-UHFFFAOYSA-N 0.000 abstract 1
- RDBONSWKYPUHCS-UHFFFAOYSA-N 1-undecyl-4,5-dihydroimidazole Chemical compound CCCCCCCCCCCN1CCN=C1 RDBONSWKYPUHCS-UHFFFAOYSA-N 0.000 abstract 1
- SCVJRXQHFJXZFZ-KVQBGUIXSA-N 2-amino-9-[(2r,4s,5r)-4-hydroxy-5-(hydroxymethyl)oxolan-2-yl]-3h-purine-6-thione Chemical compound C1=2NC(N)=NC(=S)C=2N=CN1[C@H]1C[C@H](O)[C@@H](CO)O1 SCVJRXQHFJXZFZ-KVQBGUIXSA-N 0.000 abstract 1
- LAMUXTNQCICZQX-UHFFFAOYSA-N 3-chloropropan-1-ol Chemical compound OCCCCl LAMUXTNQCICZQX-UHFFFAOYSA-N 0.000 abstract 1
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 abstract 1
- CPELXLSAUQHCOX-UHFFFAOYSA-M Bromide Chemical compound [Br-] CPELXLSAUQHCOX-UHFFFAOYSA-M 0.000 abstract 1
- CRWCMVFTFBJHCM-UHFFFAOYSA-N C1(=CC=C(C=C1)S(=O)(=O)[O-])C.C(CCCCCCCC)[NH+]1CCNCC1 Chemical compound C1(=CC=C(C=C1)S(=O)(=O)[O-])C.C(CCCCCCCC)[NH+]1CCNCC1 CRWCMVFTFBJHCM-UHFFFAOYSA-N 0.000 abstract 1
- JJEVXNCIHOTENL-UHFFFAOYSA-N C1(=CC=C(C=C1)S(=O)(=O)[O-])C.C(CCCCCCCCCCC)[SH+]C Chemical compound C1(=CC=C(C=C1)S(=O)(=O)[O-])C.C(CCCCCCCCCCC)[SH+]C JJEVXNCIHOTENL-UHFFFAOYSA-N 0.000 abstract 1
- XZXWZSNHYUMRLC-UHFFFAOYSA-N Cl(=O)(=O)(=O)[O-].[NH2+]1C=CC=C1.C1(=CC=CC=C1)C=1C(OC=CC1)=N Chemical compound Cl(=O)(=O)(=O)[O-].[NH2+]1C=CC=C1.C1(=CC=CC=C1)C=1C(OC=CC1)=N XZXWZSNHYUMRLC-UHFFFAOYSA-N 0.000 abstract 1
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 abstract 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 abstract 1
- VMHLLURERBWHNL-UHFFFAOYSA-M Sodium acetate Chemical compound [Na+].CC([O-])=O VMHLLURERBWHNL-UHFFFAOYSA-M 0.000 abstract 1
- UCKMPCXJQFINFW-UHFFFAOYSA-N Sulphide Chemical compound [S-2] UCKMPCXJQFINFW-UHFFFAOYSA-N 0.000 abstract 1
- 239000002253 acid Substances 0.000 abstract 1
- 150000001335 aliphatic alkanes Chemical class 0.000 abstract 1
- 125000005907 alkyl ester group Chemical group 0.000 abstract 1
- 125000000217 alkyl group Chemical group 0.000 abstract 1
- IYABWNGZIDDRAK-UHFFFAOYSA-N allene Chemical group C=C=C IYABWNGZIDDRAK-UHFFFAOYSA-N 0.000 abstract 1
- 125000003118 aryl group Chemical group 0.000 abstract 1
- 238000009835 boiling Methods 0.000 abstract 1
- 239000001273 butane Substances 0.000 abstract 1
- 239000007795 chemical reaction product Substances 0.000 abstract 1
- 125000004651 chloromethoxy group Chemical group ClCO* 0.000 abstract 1
- UOQACRNTVQWTFF-UHFFFAOYSA-N decane-1,10-dithiol Chemical compound SCCCCCCCCCCS UOQACRNTVQWTFF-UHFFFAOYSA-N 0.000 abstract 1
- HPNMFZURTQLUMO-UHFFFAOYSA-N diethylamine Chemical compound CCNCC HPNMFZURTQLUMO-UHFFFAOYSA-N 0.000 abstract 1
- ATUOYWHBWRKTHZ-UHFFFAOYSA-N dimethylmethane Natural products CCC ATUOYWHBWRKTHZ-UHFFFAOYSA-N 0.000 abstract 1
- 239000000839 emulsion Substances 0.000 abstract 1
- 150000002148 esters Chemical class 0.000 abstract 1
- HCFPRFJJTHMING-UHFFFAOYSA-N ethane-1,2-diamine;hydron;chloride Chemical compound [Cl-].NCC[NH3+] HCFPRFJJTHMING-UHFFFAOYSA-N 0.000 abstract 1
- 238000001914 filtration Methods 0.000 abstract 1
- 150000002430 hydrocarbons Chemical group 0.000 abstract 1
- XMBWDFGMSWQBCA-UHFFFAOYSA-N hydrogen iodide Chemical compound I XMBWDFGMSWQBCA-UHFFFAOYSA-N 0.000 abstract 1
- KFZMGEQAYNKOFK-UHFFFAOYSA-N isopropyl alcohol Natural products CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 abstract 1
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Natural products C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 abstract 1
- 125000001570 methylene group Chemical group [H]C([H])([*:1])[*:2] 0.000 abstract 1
- 239000000203 mixture Substances 0.000 abstract 1
- QAORMLJQCDFQBB-UHFFFAOYSA-N n,n-diethylethanamine;perchloric acid Chemical compound [O-]Cl(=O)(=O)=O.CC[NH+](CC)CC QAORMLJQCDFQBB-UHFFFAOYSA-N 0.000 abstract 1
- DXTFDUQLVRLXLM-UHFFFAOYSA-N n,n-dimethyldodecan-1-amine;perchloric acid Chemical compound OCl(=O)(=O)=O.CCCCCCCCCCCCN(C)C DXTFDUQLVRLXLM-UHFFFAOYSA-N 0.000 abstract 1
- ZWRDBWDXRLPESY-UHFFFAOYSA-N n-benzyl-n-ethylethanamine Chemical compound CCN(CC)CC1=CC=CC=C1 ZWRDBWDXRLPESY-UHFFFAOYSA-N 0.000 abstract 1
- DIOQZVSQGTUSAI-UHFFFAOYSA-N n-butylhexane Natural products CCCCCCCCCC DIOQZVSQGTUSAI-UHFFFAOYSA-N 0.000 abstract 1
- LDELZSZVJXFFIE-UHFFFAOYSA-N n-ethyl-n-methylethanamine;4-methylbenzenesulfonic acid Chemical compound CCN(C)CC.CC1=CC=C(S(O)(=O)=O)C=C1 LDELZSZVJXFFIE-UHFFFAOYSA-N 0.000 abstract 1
- OFBQJSOFQDEBGM-UHFFFAOYSA-N n-pentane Natural products CCCCC OFBQJSOFQDEBGM-UHFFFAOYSA-N 0.000 abstract 1
- ZVEZMVFBMOOHAT-UHFFFAOYSA-N nonane-1-thiol Chemical compound CCCCCCCCCS ZVEZMVFBMOOHAT-UHFFFAOYSA-N 0.000 abstract 1
- BKUGMZHCBXZVJB-UHFFFAOYSA-N nonyl 4-methylbenzenesulfonate Chemical compound CCCCCCCCCOS(=O)(=O)C1=CC=C(C)C=C1 BKUGMZHCBXZVJB-UHFFFAOYSA-N 0.000 abstract 1
- RGSFGYAAUTVSQA-UHFFFAOYSA-N pentamethylene Natural products C1CCCC1 RGSFGYAAUTVSQA-UHFFFAOYSA-N 0.000 abstract 1
- 125000004817 pentamethylene group Chemical group [H]C([H])([*:2])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[*:1] 0.000 abstract 1
- 229910000073 phosphorus hydride Inorganic materials 0.000 abstract 1
- JRRBJSPQEVZLPI-UHFFFAOYSA-N piperazin-1-ium;hydroxide Chemical compound O.C1CNCCN1 JRRBJSPQEVZLPI-UHFFFAOYSA-N 0.000 abstract 1
- 229960003641 piperazine hydrate Drugs 0.000 abstract 1
- 230000001376 precipitating effect Effects 0.000 abstract 1
- 239000000047 product Substances 0.000 abstract 1
- 239000001294 propane Substances 0.000 abstract 1
- 239000004332 silver Substances 0.000 abstract 1
- 229910052709 silver Inorganic materials 0.000 abstract 1
- 239000001632 sodium acetate Substances 0.000 abstract 1
- 235000017281 sodium acetate Nutrition 0.000 abstract 1
- ODZPKZBBUMBTMG-UHFFFAOYSA-N sodium amide Chemical compound [NH2-].[Na+] ODZPKZBBUMBTMG-UHFFFAOYSA-N 0.000 abstract 1
- 150000005846 sugar alcohols Polymers 0.000 abstract 1
- JOXIMZWYDAKGHI-UHFFFAOYSA-M toluene-4-sulfonate Chemical compound CC1=CC=C(S([O-])(=O)=O)C=C1 JOXIMZWYDAKGHI-UHFFFAOYSA-M 0.000 abstract 1
- PRYDGNPXVINHFJ-UHFFFAOYSA-N triethylphosphane;hydrobromide Chemical compound [Br-].CC[PH+](CC)CC PRYDGNPXVINHFJ-UHFFFAOYSA-N 0.000 abstract 1
- 125000003258 trimethylene group Chemical group [H]C([H])([*:2])C([H])([H])C([H])([H])[*:1] 0.000 abstract 1
- 125000006839 xylylene group Chemical group 0.000 abstract 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
- G03C1/08—Sensitivity-increasing substances
- G03C1/10—Organic substances
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B65—CONVEYING; PACKING; STORING; HANDLING THIN OR FILAMENTARY MATERIAL
- B65B—MACHINES, APPARATUS OR DEVICES FOR, OR METHODS OF, PACKAGING ARTICLES OR MATERIALS; UNPACKING
- B65B19/00—Packaging rod-shaped or tubular articles susceptible to damage by abrasion or pressure, e.g. cigarettes, cigars, macaroni, spaghetti, drinking straws or welding electrodes
- B65B19/02—Packaging cigarettes
- B65B19/04—Arranging, feeding, or orientating the cigarettes
- B65B19/10—Arranging cigarettes in layers each comprising a predetermined number
Landscapes
- Engineering & Computer Science (AREA)
- Physics & Mathematics (AREA)
- Chemical & Material Sciences (AREA)
- Mechanical Engineering (AREA)
- Spectroscopy & Molecular Physics (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Materials Engineering (AREA)
- General Physics & Mathematics (AREA)
- Silver Salt Photography Or Processing Solution Therefor (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Pyridine Compounds (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US321594A US2288226A (en) | 1940-02-29 | 1940-02-29 | Photographic emulsion |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| GB558710A true GB558710A (en) | 1944-01-18 |
Family
ID=23251222
Family Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| GB272/42A Expired GB557178A (en) | 1940-02-29 | 1942-01-07 | Improvements in and relating to photographic sensitive emulsions |
| GB271/42A Expired GB558710A (en) | 1940-02-29 | 1942-01-07 | Improvements in and relating to sensitive photographic materials |
Family Applications Before (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| GB272/42A Expired GB557178A (en) | 1940-02-29 | 1942-01-07 | Improvements in and relating to photographic sensitive emulsions |
Country Status (4)
| Country | Link |
|---|---|
| US (1) | US2288226A (enrdf_load_stackoverflow) |
| BE (1) | BE463680A (enrdf_load_stackoverflow) |
| FR (2) | FR949230A (enrdf_load_stackoverflow) |
| GB (2) | GB557178A (enrdf_load_stackoverflow) |
Cited By (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2944902A (en) * | 1956-07-30 | 1960-07-12 | Eastman Kodak Co | Sensitization of photographic emulsions with ionic polyalkylene oxide salts |
| US3113026A (en) * | 1959-01-19 | 1963-12-03 | Gen Aniline & Film Corp | Polyvinyl alcohol photographic silver halide emulsions |
| EP0124795A3 (en) * | 1983-04-11 | 1988-01-13 | Fuji Photo Film Co., Ltd. | Silver halide photographic emulsion |
| GB2230263A (en) * | 1989-04-10 | 1990-10-17 | Tobishi Pharmaceutical Co | Quaternary ammonium compounds having muscle relaxation activity |
Families Citing this family (22)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2449153A (en) * | 1944-04-03 | 1948-09-14 | Urbach Franz | Photographic silver bromide emulsion sensitized with cysteine |
| BE514795A (enrdf_load_stackoverflow) * | 1951-10-17 | |||
| US2784090A (en) * | 1952-11-08 | 1957-03-05 | Eastman Kodak Co | Stabilization of emulsions sensitized with onium compounds |
| BE553032A (enrdf_load_stackoverflow) * | 1955-12-01 | |||
| US2944900A (en) * | 1956-12-10 | 1960-07-12 | Eastman Kodak Co | Sensitization of photographic emulsions with ionic polyalkyene oxide salts |
| US3062645A (en) * | 1957-11-27 | 1962-11-06 | Eastman Kodak Co | Sensitization of photographic emulsions to be developed with p-phenylenediamine developing agents |
| US2940851A (en) * | 1957-11-27 | 1960-06-14 | Eastman Kodak Co | Sensitization of photographic emulsions |
| US3100704A (en) * | 1958-07-24 | 1963-08-13 | Gen Aniline & Film Corp | Photographic materials containing carbodhmides |
| US3046135A (en) * | 1958-12-12 | 1962-07-24 | Eastman Kodak Co | Sensitization of photographic silver halide emulsions with sulfur-containing polymers |
| BE620339A (enrdf_load_stackoverflow) * | 1961-07-18 | |||
| US3330658A (en) * | 1963-12-20 | 1967-07-11 | Eastman Kodak Co | Photographic silver halide diffusion transfer process |
| US3893862A (en) * | 1973-09-24 | 1975-07-08 | Eastman Kodak Co | Reduced pyridine compounds |
| GB1491902A (en) * | 1974-02-28 | 1977-11-16 | Agfa Gevaert | Development of exposed lith-emulsions |
| JPS59116647A (ja) | 1982-12-13 | 1984-07-05 | Konishiroku Photo Ind Co Ltd | ハロゲン化銀写真感光材料 |
| JPS59142541A (ja) * | 1983-02-02 | 1984-08-15 | Fuji Photo Film Co Ltd | ハロゲン化銀写真乳剤 |
| JPS60136738A (ja) * | 1983-12-22 | 1985-07-20 | Fuji Photo Film Co Ltd | ハロゲン化銀写真感光材料 |
| US5013622A (en) * | 1986-12-12 | 1991-05-07 | Minnesota Mining And Manufacturing Company | Supersensitization of silver halide emulsions |
| US4873184A (en) * | 1988-02-05 | 1989-10-10 | Minnesota Mining And Manufacturing Company | Supersensitization of silver halide photothermographic emulsions |
| US5536634A (en) * | 1994-09-30 | 1996-07-16 | Eastman Kodak Company | Silver halide emulsions spectrally sensitized in the presence of low N-alkyl pyridinium ions |
| EP0967086B1 (de) | 1998-06-18 | 2001-03-21 | ILFORD Imaging Switzerland GmbH | Aufzeichnungsmaterialien für den Tintenstrahldruck |
| US6071688A (en) * | 1998-07-29 | 2000-06-06 | Eastman Kodak Company | Providing additives to a coating composition by vaporization |
| CN112154757B (zh) * | 2020-09-30 | 2022-08-30 | 福建泉智生物科技有限公司 | 枇杷有机-无机质平衡施肥方法 |
-
0
- BE BE463680D patent/BE463680A/xx unknown
-
1940
- 1940-02-29 US US321594A patent/US2288226A/en not_active Expired - Lifetime
-
1942
- 1942-01-07 GB GB272/42A patent/GB557178A/en not_active Expired
- 1942-01-07 GB GB271/42A patent/GB558710A/en not_active Expired
-
1945
- 1945-08-11 FR FR949230D patent/FR949230A/fr not_active Expired
-
1947
- 1947-05-05 FR FR949680D patent/FR949680A/fr not_active Expired
Cited By (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2944902A (en) * | 1956-07-30 | 1960-07-12 | Eastman Kodak Co | Sensitization of photographic emulsions with ionic polyalkylene oxide salts |
| US3113026A (en) * | 1959-01-19 | 1963-12-03 | Gen Aniline & Film Corp | Polyvinyl alcohol photographic silver halide emulsions |
| EP0124795A3 (en) * | 1983-04-11 | 1988-01-13 | Fuji Photo Film Co., Ltd. | Silver halide photographic emulsion |
| GB2230263A (en) * | 1989-04-10 | 1990-10-17 | Tobishi Pharmaceutical Co | Quaternary ammonium compounds having muscle relaxation activity |
| US5093370A (en) * | 1989-04-10 | 1992-03-03 | Tobishi Yakuhin Kogyo Kabushiki Kaisha | Quaternary ammonium compounds having muscle relaxation activity |
Also Published As
| Publication number | Publication date |
|---|---|
| GB557178A (en) | 1943-11-09 |
| US2288226A (en) | 1942-06-30 |
| FR949230A (fr) | 1949-08-24 |
| FR949680A (fr) | 1949-09-06 |
| BE463680A (enrdf_load_stackoverflow) |
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