US3469979A - Electrophotographic recording element with increased speed - Google Patents
Electrophotographic recording element with increased speed Download PDFInfo
- Publication number
- US3469979A US3469979A US510089A US3469979DA US3469979A US 3469979 A US3469979 A US 3469979A US 510089 A US510089 A US 510089A US 3469979D A US3469979D A US 3469979DA US 3469979 A US3469979 A US 3469979A
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- US
- United States
- Prior art keywords
- thiourea
- recording element
- coating
- hypersensitizer
- dye
- 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
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- XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 description 26
- UMGDCJDMYOKAJW-UHFFFAOYSA-N thiourea Chemical compound NC(N)=S UMGDCJDMYOKAJW-UHFFFAOYSA-N 0.000 description 23
- 239000000975 dye Substances 0.000 description 22
- 238000000576 coating method Methods 0.000 description 20
- 239000011248 coating agent Substances 0.000 description 19
- 229910052757 nitrogen Inorganic materials 0.000 description 13
- 239000011787 zinc oxide Substances 0.000 description 13
- 238000000034 method Methods 0.000 description 9
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Natural products NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 8
- -1 Thiourea 1,3 bis (carboxypentyl) thiourea Chemical compound 0.000 description 7
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 7
- 239000000203 mixture Substances 0.000 description 6
- 230000001235 sensitizing effect Effects 0.000 description 6
- ZQGWBPQBZHMUFG-UHFFFAOYSA-N 1,1-dimethylthiourea Chemical compound CN(C)C(N)=S ZQGWBPQBZHMUFG-UHFFFAOYSA-N 0.000 description 4
- RYYXDZDBXNUPOG-UHFFFAOYSA-N 4,5,6,7-tetrahydro-1,3-benzothiazole-2,6-diamine;dihydrochloride Chemical compound Cl.Cl.C1C(N)CCC2=C1SC(N)=N2 RYYXDZDBXNUPOG-UHFFFAOYSA-N 0.000 description 4
- 239000000654 additive Substances 0.000 description 4
- 230000000996 additive effect Effects 0.000 description 4
- 239000011230 binding agent Substances 0.000 description 4
- 125000004177 diethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 4
- 125000000118 dimethyl group Chemical group [H]C([H])([H])* 0.000 description 4
- 238000009472 formulation Methods 0.000 description 4
- 125000003944 tolyl group Chemical group 0.000 description 4
- 125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 description 3
- PDQAZBWRQCGBEV-UHFFFAOYSA-N Ethylenethiourea Chemical compound S=C1NCCN1 PDQAZBWRQCGBEV-UHFFFAOYSA-N 0.000 description 3
- 125000002252 acyl group Chemical group 0.000 description 3
- 125000001931 aliphatic group Chemical group 0.000 description 3
- 125000003118 aryl group Chemical group 0.000 description 3
- UDIUIXIBBPOQKL-UHFFFAOYSA-N aziridine-1-carbothioamide Chemical compound NC(=S)N1CC1 UDIUIXIBBPOQKL-UHFFFAOYSA-N 0.000 description 3
- 125000000623 heterocyclic group Chemical group 0.000 description 3
- 229910052739 hydrogen Inorganic materials 0.000 description 3
- 239000001257 hydrogen Substances 0.000 description 3
- 125000004435 hydrogen atom Chemical class [H]* 0.000 description 3
- 239000002245 particle Substances 0.000 description 3
- 239000011347 resin Substances 0.000 description 3
- 229920005989 resin Polymers 0.000 description 3
- AZERQDZCGIDXHT-UHFFFAOYSA-N 1,1-dicyclohexylthiourea Chemical compound C1CCCCC1N(C(=S)N)C1CCCCC1 AZERQDZCGIDXHT-UHFFFAOYSA-N 0.000 description 2
- SNQABJUAAUNSEJ-UHFFFAOYSA-N 1,3-bis(4-fluorophenyl)thiourea Chemical compound C1=CC(F)=CC=C1NC(=S)NC1=CC=C(F)C=C1 SNQABJUAAUNSEJ-UHFFFAOYSA-N 0.000 description 2
- KREOCUNMMFZOOS-UHFFFAOYSA-N 1,3-di(propan-2-yl)thiourea Chemical compound CC(C)NC(S)=NC(C)C KREOCUNMMFZOOS-UHFFFAOYSA-N 0.000 description 2
- LTMHEXFMSAISLN-UHFFFAOYSA-N 1,3-ditert-butylthiourea Chemical compound CC(C)(C)NC(=S)NC(C)(C)C LTMHEXFMSAISLN-UHFFFAOYSA-N 0.000 description 2
- XNWFRZJHXBZDAG-UHFFFAOYSA-N 2-METHOXYETHANOL Chemical compound COCCO XNWFRZJHXBZDAG-UHFFFAOYSA-N 0.000 description 2
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- SGHZXLIDFTYFHQ-UHFFFAOYSA-L Brilliant Blue Chemical compound [Na+].[Na+].C=1C=C(C(=C2C=CC(C=C2)=[N+](CC)CC=2C=C(C=CC=2)S([O-])(=O)=O)C=2C(=CC=CC=2)S([O-])(=O)=O)C=CC=1N(CC)CC1=CC=CC(S([O-])(=O)=O)=C1 SGHZXLIDFTYFHQ-UHFFFAOYSA-L 0.000 description 2
- KQJQICVXLJTWQD-UHFFFAOYSA-N N-Methylthiourea Chemical compound CNC(N)=S KQJQICVXLJTWQD-UHFFFAOYSA-N 0.000 description 2
- IPCRBOOJBPETMF-UHFFFAOYSA-N N-acetylthiourea Chemical compound CC(=O)NC(N)=S IPCRBOOJBPETMF-UHFFFAOYSA-N 0.000 description 2
- XGEGHDBEHXKFPX-UHFFFAOYSA-N N-methylthiourea Natural products CNC(N)=O XGEGHDBEHXKFPX-UHFFFAOYSA-N 0.000 description 2
- SMWDFEZZVXVKRB-UHFFFAOYSA-N Quinoline Chemical compound N1=CC=CC2=CC=CC=C21 SMWDFEZZVXVKRB-UHFFFAOYSA-N 0.000 description 2
- XYLMUPLGERFSHI-UHFFFAOYSA-N alpha-Methylstyrene Chemical compound CC(=C)C1=CC=CC=C1 XYLMUPLGERFSHI-UHFFFAOYSA-N 0.000 description 2
- 235000010290 biphenyl Nutrition 0.000 description 2
- 239000004305 biphenyl Substances 0.000 description 2
- 125000006267 biphenyl group Chemical group 0.000 description 2
- 229910052799 carbon Inorganic materials 0.000 description 2
- 150000001875 compounds Chemical class 0.000 description 2
- 125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 description 2
- 239000006185 dispersion Substances 0.000 description 2
- SEACYXSIPDVVMV-UHFFFAOYSA-L eosin Y Chemical compound [Na+].[Na+].[O-]C(=O)C1=CC=CC=C1C1=C2C=C(Br)C(=O)C(Br)=C2OC2=C(Br)C([O-])=C(Br)C=C21 SEACYXSIPDVVMV-UHFFFAOYSA-L 0.000 description 2
- GNBHRKFJIUUOQI-UHFFFAOYSA-N fluorescein Chemical compound O1C(=O)C2=CC=CC=C2C21C1=CC=C(O)C=C1OC1=CC(O)=CC=C21 GNBHRKFJIUUOQI-UHFFFAOYSA-N 0.000 description 2
- 125000006203 morpholinoethyl group Chemical group [H]C([H])(*)C([H])([H])N1C([H])([H])C([H])([H])OC([H])([H])C1([H])[H] 0.000 description 2
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 2
- ZUOUZKKEUPVFJK-UHFFFAOYSA-N phenylbenzene Natural products C1=CC=CC=C1C1=CC=CC=C1 ZUOUZKKEUPVFJK-UHFFFAOYSA-N 0.000 description 2
- 230000005855 radiation Effects 0.000 description 2
- 230000035945 sensitivity Effects 0.000 description 2
- JUSFFZFOIIGLRP-UHFFFAOYSA-N 1,1-dimethyl-3-phenylthiourea Chemical compound CN(C)C(=S)NC1=CC=CC=C1 JUSFFZFOIIGLRP-UHFFFAOYSA-N 0.000 description 1
- WZEWAUCURBRHGN-UHFFFAOYSA-N 1-methoxy-1-phenylthiourea Chemical compound CON(C(N)=S)C1=CC=CC=C1 WZEWAUCURBRHGN-UHFFFAOYSA-N 0.000 description 1
- BCHZICNRHXRCHY-UHFFFAOYSA-N 2h-oxazine Chemical compound N1OC=CC=C1 BCHZICNRHXRCHY-UHFFFAOYSA-N 0.000 description 1
- MNOJRWOWILAHAV-UHFFFAOYSA-N 3-bromophenol Chemical compound OC1=CC=CC(Br)=C1 MNOJRWOWILAHAV-UHFFFAOYSA-N 0.000 description 1
- RBLUJIWKMSZIMK-UHFFFAOYSA-N 4-n-(4-methoxyphenyl)benzene-1,4-diamine Chemical class C1=CC(OC)=CC=C1NC1=CC=C(N)C=C1 RBLUJIWKMSZIMK-UHFFFAOYSA-N 0.000 description 1
- HVXJATBZGHEZIQ-UHFFFAOYSA-N 6-(5-carboxypentylcarbamothioylamino)hexanoic acid Chemical compound OC(=O)CCCCCNC(=S)NCCCCCC(O)=O HVXJATBZGHEZIQ-UHFFFAOYSA-N 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- RZSYLLSAWYUBPE-UHFFFAOYSA-L Fast green FCF Chemical compound [Na+].[Na+].C=1C=C(C(=C2C=CC(C=C2)=[N+](CC)CC=2C=C(C=CC=2)S([O-])(=O)=O)C=2C(=CC(O)=CC=2)S([O-])(=O)=O)C=CC=1N(CC)CC1=CC=CC(S([O-])(=O)=O)=C1 RZSYLLSAWYUBPE-UHFFFAOYSA-L 0.000 description 1
- KFFQABQEJATQAT-UHFFFAOYSA-N N,N'-dibutylthiourea Chemical compound CCCCNC(=S)NCCCC KFFQABQEJATQAT-UHFFFAOYSA-N 0.000 description 1
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 1
- PJANXHGTPQOBST-VAWYXSNFSA-N Stilbene Natural products C=1C=CC=CC=1/C=C/C1=CC=CC=C1 PJANXHGTPQOBST-VAWYXSNFSA-N 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- ZXGIHDNEIWPDFW-UHFFFAOYSA-M acid red 4 Chemical compound [Na+].COC1=CC=CC=C1N=NC1=CC(S([O-])(=O)=O)=C(C=CC=C2)C2=C1O ZXGIHDNEIWPDFW-UHFFFAOYSA-M 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- UDSAIICHUKSCKT-UHFFFAOYSA-N bromophenol blue Chemical compound C1=C(Br)C(O)=C(Br)C=C1C1(C=2C=C(Br)C(O)=C(Br)C=2)C2=CC=CC=C2S(=O)(=O)O1 UDSAIICHUKSCKT-UHFFFAOYSA-N 0.000 description 1
- 150000001721 carbon Chemical group 0.000 description 1
- 238000007600 charging Methods 0.000 description 1
- 239000008199 coating composition Substances 0.000 description 1
- BASONKABNAOEDG-UHFFFAOYSA-L disodium;5-[(1-anilino-1,3-dioxobutan-2-yl)diazenyl]-2-[4-[(1-anilino-1,3-dioxobutan-2-yl)diazenyl]-5-methyl-2-sulfonatophenyl]-4-methylbenzenesulfonate Chemical compound [Na+].[Na+].C=1C=CC=CC=1NC(=O)C(C(=O)C)N=NC(C(=C1)C)=CC(S([O-])(=O)=O)=C1C(C(=C1)S([O-])(=O)=O)=CC(C)=C1N=NC(C(C)=O)C(=O)NC1=CC=CC=C1 BASONKABNAOEDG-UHFFFAOYSA-L 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000007786 electrostatic charging Methods 0.000 description 1
- YQGOJNYOYNNSMM-UHFFFAOYSA-N eosin Chemical compound [Na+].OC(=O)C1=CC=CC=C1C1=C2C=C(Br)C(=O)C(Br)=C2OC2=C(Br)C(O)=C(Br)C=C21 YQGOJNYOYNNSMM-UHFFFAOYSA-N 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 125000001434 methanylylidene group Chemical group [H]C#[*] 0.000 description 1
- CXKWCBBOMKCUKX-UHFFFAOYSA-M methylene blue Chemical compound [Cl-].C1=CC(N(C)C)=CC2=[S+]C3=CC(N(C)C)=CC=C3N=C21 CXKWCBBOMKCUKX-UHFFFAOYSA-M 0.000 description 1
- 229960000907 methylthioninium chloride Drugs 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- FZIOOTTWDRFBKU-UHFFFAOYSA-N n,4-dimethylbenzamide Chemical compound CNC(=O)C1=CC=C(C)C=C1 FZIOOTTWDRFBKU-UHFFFAOYSA-N 0.000 description 1
- SNICXCGAKADSCV-UHFFFAOYSA-N nicotine Chemical compound CN1CCCC1C1=CC=CN=C1 SNICXCGAKADSCV-UHFFFAOYSA-N 0.000 description 1
- 125000004433 nitrogen atom Chemical group N* 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 229920000058 polyacrylate Polymers 0.000 description 1
- 235000012752 quinoline yellow Nutrition 0.000 description 1
- IZMJMCDDWKSTTK-UHFFFAOYSA-N quinoline yellow Chemical compound C1=CC=CC2=NC(C3C(C4=CC=CC=C4C3=O)=O)=CC=C21 IZMJMCDDWKSTTK-UHFFFAOYSA-N 0.000 description 1
- 229940051201 quinoline yellow Drugs 0.000 description 1
- 239000004172 quinoline yellow Substances 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 239000000992 solvent dye Substances 0.000 description 1
- PJANXHGTPQOBST-UHFFFAOYSA-N stilbene Chemical compound C=1C=CC=CC=1C=CC1=CC=CC=C1 PJANXHGTPQOBST-UHFFFAOYSA-N 0.000 description 1
- 235000021286 stilbenes Nutrition 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 125000001424 substituent group Chemical group 0.000 description 1
- 229910052717 sulfur Inorganic materials 0.000 description 1
- 125000004434 sulfur atom Chemical group 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
- MPCYPRXRVWZKGF-UHFFFAOYSA-J tetrasodium 5-amino-3-[[4-[4-[(8-amino-1-hydroxy-3,6-disulfonatonaphthalen-2-yl)diazenyl]phenyl]phenyl]diazenyl]-4-hydroxynaphthalene-2,7-disulfonate Chemical compound [Na+].[Na+].[Na+].[Na+].C1=C(S([O-])(=O)=O)C=C2C=C(S([O-])(=O)=O)C(N=NC3=CC=C(C=C3)C3=CC=C(C=C3)N=NC3=C(C=C4C=C(C=C(C4=C3O)N)S([O-])(=O)=O)S([O-])(=O)=O)=C(O)C2=C1N MPCYPRXRVWZKGF-UHFFFAOYSA-J 0.000 description 1
- 150000003585 thioureas Chemical class 0.000 description 1
- 229910052725 zinc Inorganic materials 0.000 description 1
Classifications
-
- G—PHYSICS
- G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
- G03G—ELECTROGRAPHY; ELECTROPHOTOGRAPHY; MAGNETOGRAPHY
- G03G5/00—Recording members for original recording by exposure, e.g. to light, to heat, to electrons; Manufacture thereof; Selection of materials therefor
- G03G5/02—Charge-receiving layers
- G03G5/04—Photoconductive layers; Charge-generation layers or charge-transporting layers; Additives therefor; Binders therefor
- G03G5/06—Photoconductive layers; Charge-generation layers or charge-transporting layers; Additives therefor; Binders therefor characterised by the photoconductive material being organic
- G03G5/0664—Dyes
-
- G—PHYSICS
- G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
- G03G—ELECTROGRAPHY; ELECTROPHOTOGRAPHY; MAGNETOGRAPHY
- G03G5/00—Recording members for original recording by exposure, e.g. to light, to heat, to electrons; Manufacture thereof; Selection of materials therefor
- G03G5/02—Charge-receiving layers
- G03G5/04—Photoconductive layers; Charge-generation layers or charge-transporting layers; Additives therefor; Binders therefor
- G03G5/06—Photoconductive layers; Charge-generation layers or charge-transporting layers; Additives therefor; Binders therefor characterised by the photoconductive material being organic
- G03G5/0601—Acyclic or carbocyclic compounds
- G03G5/062—Acyclic or carbocyclic compounds containing non-metal elements other than hydrogen, halogen, oxygen or nitrogen
-
- G—PHYSICS
- G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
- G03G—ELECTROGRAPHY; ELECTROPHOTOGRAPHY; MAGNETOGRAPHY
- G03G5/00—Recording members for original recording by exposure, e.g. to light, to heat, to electrons; Manufacture thereof; Selection of materials therefor
- G03G5/02—Charge-receiving layers
- G03G5/04—Photoconductive layers; Charge-generation layers or charge-transporting layers; Additives therefor; Binders therefor
- G03G5/06—Photoconductive layers; Charge-generation layers or charge-transporting layers; Additives therefor; Binders therefor characterised by the photoconductive material being organic
- G03G5/0622—Heterocyclic compounds
- G03G5/0624—Heterocyclic compounds containing one hetero ring
- G03G5/0627—Heterocyclic compounds containing one hetero ring being five-membered
- G03G5/0631—Heterocyclic compounds containing one hetero ring being five-membered containing two hetero atoms
-
- G—PHYSICS
- G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
- G03G—ELECTROGRAPHY; ELECTROPHOTOGRAPHY; MAGNETOGRAPHY
- G03G5/00—Recording members for original recording by exposure, e.g. to light, to heat, to electrons; Manufacture thereof; Selection of materials therefor
- G03G5/02—Charge-receiving layers
- G03G5/04—Photoconductive layers; Charge-generation layers or charge-transporting layers; Additives therefor; Binders therefor
- G03G5/06—Photoconductive layers; Charge-generation layers or charge-transporting layers; Additives therefor; Binders therefor characterised by the photoconductive material being organic
- G03G5/0622—Heterocyclic compounds
- G03G5/0624—Heterocyclic compounds containing one hetero ring
- G03G5/0635—Heterocyclic compounds containing one hetero ring being six-membered
- G03G5/0638—Heterocyclic compounds containing one hetero ring being six-membered containing two hetero atoms
-
- G—PHYSICS
- G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
- G03G—ELECTROGRAPHY; ELECTROPHOTOGRAPHY; MAGNETOGRAPHY
- G03G5/00—Recording members for original recording by exposure, e.g. to light, to heat, to electrons; Manufacture thereof; Selection of materials therefor
- G03G5/02—Charge-receiving layers
- G03G5/04—Photoconductive layers; Charge-generation layers or charge-transporting layers; Additives therefor; Binders therefor
- G03G5/09—Sensitisors or activators, e.g. dyestuffs
Definitions
- This invention relates to electrophotography and has for its principal object provision of photoconductive recording elements and recording processes with increased speed of discharge upon exposure to light.
- Electrophotography is well known and involves generally the electrostatic charging in the dark of a photoconductive layer of a recording element, and exposing the layer to a pattern of light to which the photoconductor is sensitive, thereby forming a latent image as an electrostatic charge pattern in areas not receiving light.
- the resulting image can be electronically scanned or displayed but is usually developed to a visible image with electroscopic colored particles. The particles can then be fixed, if desired, either to the recording element itself or to a receiving surface to which they are transferred.
- Recording elements comprising finely divided photoconductive particles dispersed in insulating resinous binders are known and are disclosed in US. Patent No. 3,121,006. Photoconductive zinc oxide in a binder is generally used and such recording elements are more specifically disclosed in US. Patent No. 3,052,539. Such recording elements are known to be sensitive to ultraviolet radiation at wavelengths of 3-800 angstroms or lower. Sensitivity refers to the capacity of the photoconductor of the recording element to dissipate electrostatic charges on its surface by a lowering of its resistivity at specified wave lengths of light.
- the recording elements be sensitive to light at visible Wavelengths includingSOOO to 5500 angstroms. This can be accomplished by adding dye of known type as disclosed for example in the above two patents. However, dyes or a United States Patent 0 3,469,979 Patented Sept. 30, 1969:
- hypersensitization permits use of a lesser amount of dye, a greater variety of dyes, and permits formulation of zinc oxide coatings which are more nearly White in appearance.
- the amount of the hypersensitizer additive is not critical and the nature of the N substituents, provided they are substantially non-reactive in the coating, is not important, a large number including substantially all types currently available having been found to be useful.
- the present invention comprises an improved electrophotographic recording element comprising a backing and a coating of finely-divided zinc oxide and finely divided sensitizing dye therefor dispersed in an insulating binder wherein the improvement consists in the dispersion within the coating of an eflective amount of a hypersensitizer for increasing the speed of discharge of the coating when electrostatically charged and exposed to light, said sensitizer consisting essentially of (a) thiourea dioxide, or (b) a compound of the structure wherein each of R R R R3 or R is selected from the group consisting of hydrogen, lower aliphatic, lower cycloaliphatic, lower acyl, aryl, and heterocyclic monovalent radicals and R and R are lower divalent aliphatic radicals.
- the invention comprises the method of producing a latent electrostatic image comprising applying a uniform electrostatic charge to the above improved recording element in the dark, that is, the absence of radiation to which the photoconductor is sensitive, and exposing the element to a pattern of light to which the photoconductor is sensitive.
- the effect of the hypersensitizer is shown in the following examples, the compositions stated being coated onto paper 0.0022 inch in thickness and having a resistivity at 20% relative humidity of 1000 megohms.
- the coating compositions were applied and dried to a thickness of about 0.0008 inch. After storage in the dark at 20% R.H., they were charged to approximately 500 volts using a negative corona at 7.4 kv. grounded with a positive corona of 3.0 kv.
- the discharge time was the time in seconds to discharge to 5 volts upon exposure to 2.0 foot candles of light from a General Electric Photo flood lamp EPR of 375 watts. The time lapse between charging' and exposure in each case was about 8 seconds. Voltages were measured as apparent surface voltage with the equipment and procedure described in E. Giamo, RCA Review, volume XXII, No. 4, pages 780-790 of December 1961. All parts are by weight except where otherwise indicated.
- N,N -ethylenethiourea N methyl thiourea N,N dimethyl thiourea 1,3 diethyl, 2 thiourea 1,3 dibutyl thiourea N acetyl thiourea. 1 allyl, 2 thiourea 3 allyl1,1 diethyl, 2 thiourea 1 phenyl, 2 thiourea 1,1 diphenyl, 2 thiourea N,N dicyclohexyl thiourea.
- N,N dimethyl N (p tolyl) thiourea Thiourea dioxide 23-- O methoxyphenyl thiourea 24 N,N dimethyl thiourea
- the zinc oxide was Florence Green Seal No. 8 of the New Jersey Zinc Co.
- Acryloid B-82 as a 40% solution in toluene of an acrylic polymer from Rohm and Haas Co.
- the alpha-methyl styrene was 4 Resin 276 V2 of the Dow Chemical Company
- the sensitizing dye solution had the following composition:
- Eosin 0 Acid Red 87 (a hydroxyphthalein dye), 1% Calco fiuorescein, Acid Yellow 73, 1% Brom phenol blue (3,3,3,5-tetrabrorno-phenol sulphionphthalein), 1% 0.26 Brilliant Yellow 6G, 1% 0.84
- the samples were prepared by dispersing the zinc oxide in the solvent, adding the resins, dye solution, and hypersensitizer, the resulting suspension coated onto the paper base and the coating dried, for example for one minute at C.
- Examples 25-33 were prepared using the Zinc oxide and resin formulation and procedure of Examples 1-24 but substituting the indicated dyes and additive in the quantity of toluene solvent indicated in ml. Exposure time was the time in seconds to discharge to 5 volts apparent surface voltage.
- Hypersensi- Initial Exposure Solvent Dye tizer charge time The dye employed in Examples 25-33 was a 1% solution of Calco Florescein of the American Cyanamid Co. in methyl Cellosolve, the amounts indicated being in ml.
- the hypersensitizer was 2 mercapto imidazoline, the amount being in grams. At 3 ml. of dye solution, the zinc oxide coating exhibited some color. While these data show that amount is not critical, Example 29 with 1.0 part by weight hypersensitizer per parts zinc oxide with minimum dye is preferred.
- Examples 34 to 61 were prepared using Formula B of Examples 1 to 24 together with the dyes indicated in the following Examples 34 to 61, the dye amounts being in ml. of a 1% solution of the dye in methyl Cellosolve.
- An improved electrophotographic recording element comprising a backing and a coating thereon of finely divided photoconductive zinc oxide and sensitizing dyes therefor dispersed in an insulating binder wherein the improvement consists in the dispersion within the coating of an effective amount of a hypersensitizer for increasing the speed of discharge of the coating when electrostatically charged and exposed to light, said hypersensitizer selected from the group consisting essentially of (a) thiourea dioxide or (b) a compound having the structure wherein each of R R R R and R is selected from the group consisting of hydrogen, lower aliphatic, lower cycloaliphatic, lower acyl, aryl, and heterocyclic monovalent radicals and R and R are lower divalent aliphatic radicals, said heterocyclic radical consisting essentially of a six-membered ring of carbon, nitrogen and oxygen.
- a hypersensitizer selected from the group consisting essentially of (a) thiourea dioxide or (b) a compound having the
- a recording element wherein said backing is paper and said hypersensitizer is selected from the group consisting of N,N-ethylenethiourea; N methyl thiourea; N,N dimethyl thiourea; 1,3 diethyl, 2 thiourea; 1,3 dibutyl thiourea; N acetyl thiourea; 1 allyl, 2 thiourea; 3 allyl 1, 1 diethyl, 2 thiourea; 1 phenyl, 2 thiourea; 1,1 diphenyl, 2 thiourea; N,N dicyclohexyl thiourea; 1 cyclohexyl, 3(2 morpholinoethyl) thiourea; thiourea; 1,3 bis (carboxypentyl) thiourea; N,N bis (4 fluorophenyl) thiourea; N,N di tert-butyl thioure
- the method of producing a latent electrostatic image which comprises applying a uniform electrostatic charge in the dark to the coating of the recording element of claim 1 and exposing the coating to a pattern of light.
- the method of producing a latent electrostatic image which comprises applying a uniform electrostatic charge in the dark to the coating of the recording element of claim 2 and exposing the coating to a pattern of light.
- the method of producing a latent electrostatic image which comprises applying a uniform electrostatic charge in the dark to the coating of the recording element of claim 3 and exposing the coating to a pattern of light.
- the method of producing a latent electrostatic image which comprises applying a uniform electrostatic charge in the dark to the coating of the recording element of claim 4 and exposing the coating to a pattern of light.
Landscapes
- Physics & Mathematics (AREA)
- General Physics & Mathematics (AREA)
- Photoreceptors In Electrophotography (AREA)
- Heat Sensitive Colour Forming Recording (AREA)
- Non-Silver Salt Photosensitive Materials And Non-Silver Salt Photography (AREA)
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US51008965A | 1965-11-26 | 1965-11-26 |
Publications (1)
Publication Number | Publication Date |
---|---|
US3469979A true US3469979A (en) | 1969-09-30 |
Family
ID=24029334
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US510089A Expired - Lifetime US3469979A (en) | 1965-11-26 | 1965-11-26 | Electrophotographic recording element with increased speed |
Country Status (6)
Country | Link |
---|---|
US (1) | US3469979A (enrdf_load_html_response) |
BE (1) | BE690270A (enrdf_load_html_response) |
DE (1) | DE1522576B2 (enrdf_load_html_response) |
FR (1) | FR1501634A (enrdf_load_html_response) |
GB (1) | GB1128479A (enrdf_load_html_response) |
NL (1) | NL6616727A (enrdf_load_html_response) |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4820620A (en) * | 1986-07-17 | 1989-04-11 | Minnesota Mining And Manufacturing Company | Supersensitization of and reduction of dark decay rate in photoconductive films |
US4911999A (en) * | 1988-12-13 | 1990-03-27 | E. I. Du Pont De Nemours And Company | Electrostatic master containing thiourea or thioamide electrostatic decay additive for high speed xeroprinting |
US5185227A (en) * | 1990-08-28 | 1993-02-09 | Oji Paper Co., Ltd. | Electrophotographic lithograph printing plate material |
Families Citing this family (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5865438A (ja) * | 1981-10-15 | 1983-04-19 | Fuji Photo Film Co Ltd | 光導電性組成物およびそれを用いた電子写真感光材料 |
Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3031301A (en) * | 1959-03-30 | 1962-04-24 | Gen Electric | Photosensitive resin compositions |
US3352670A (en) * | 1964-02-14 | 1967-11-14 | Minnesota Mining & Mfg | Supersensitizers for optically sensitized photoconductive layers |
-
1965
- 1965-11-26 US US510089A patent/US3469979A/en not_active Expired - Lifetime
-
1966
- 1966-11-25 BE BE690270D patent/BE690270A/xx unknown
- 1966-11-25 FR FR85106A patent/FR1501634A/fr not_active Expired
- 1966-11-25 GB GB52821/66A patent/GB1128479A/en not_active Expired
- 1966-11-25 DE DE19661522576 patent/DE1522576B2/de active Pending
- 1966-11-28 NL NL6616727A patent/NL6616727A/xx unknown
Patent Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3031301A (en) * | 1959-03-30 | 1962-04-24 | Gen Electric | Photosensitive resin compositions |
US3352670A (en) * | 1964-02-14 | 1967-11-14 | Minnesota Mining & Mfg | Supersensitizers for optically sensitized photoconductive layers |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4820620A (en) * | 1986-07-17 | 1989-04-11 | Minnesota Mining And Manufacturing Company | Supersensitization of and reduction of dark decay rate in photoconductive films |
US4911999A (en) * | 1988-12-13 | 1990-03-27 | E. I. Du Pont De Nemours And Company | Electrostatic master containing thiourea or thioamide electrostatic decay additive for high speed xeroprinting |
US5185227A (en) * | 1990-08-28 | 1993-02-09 | Oji Paper Co., Ltd. | Electrophotographic lithograph printing plate material |
Also Published As
Publication number | Publication date |
---|---|
DE1522576A1 (de) | 1970-02-26 |
NL6616727A (enrdf_load_html_response) | 1967-05-29 |
FR1501634A (fr) | 1967-11-10 |
BE690270A (enrdf_load_html_response) | 1967-05-25 |
GB1128479A (en) | 1968-09-25 |
DE1522576B2 (de) | 1971-04-29 |
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