US3708294A - Process for preparing a photoconductive fiber sheet - Google Patents
Process for preparing a photoconductive fiber sheet Download PDFInfo
- Publication number
- US3708294A US3708294A US00050899A US3708294DA US3708294A US 3708294 A US3708294 A US 3708294A US 00050899 A US00050899 A US 00050899A US 3708294D A US3708294D A US 3708294DA US 3708294 A US3708294 A US 3708294A
- Authority
- US
- United States
- Prior art keywords
- photoconductive
- fiber sheet
- lewis acid
- sheet
- sensitizing
- 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
- 239000000835 fiber Substances 0.000 title abstract description 77
- 238000004519 manufacturing process Methods 0.000 title description 15
- 230000001235 sensitizing effect Effects 0.000 abstract description 54
- 150000007517 lewis acids Chemical class 0.000 abstract description 42
- 239000002841 Lewis acid Substances 0.000 abstract description 41
- 238000004043 dyeing Methods 0.000 abstract description 15
- 229920005594 polymer fiber Polymers 0.000 abstract description 2
- 238000000034 method Methods 0.000 description 33
- 238000004040 coloring Methods 0.000 description 32
- 239000003795 chemical substances by application Substances 0.000 description 21
- 239000000463 material Substances 0.000 description 20
- 239000000126 substance Substances 0.000 description 14
- 239000004744 fabric Substances 0.000 description 13
- 238000001228 spectrum Methods 0.000 description 10
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 9
- 239000002904 solvent Substances 0.000 description 7
- 206010034972 Photosensitivity reaction Diseases 0.000 description 6
- 230000036211 photosensitivity Effects 0.000 description 6
- -1 polyethylene terephthalate Polymers 0.000 description 6
- 239000002861 polymer material Substances 0.000 description 6
- 230000003595 spectral effect Effects 0.000 description 6
- 238000002166 wet spinning Methods 0.000 description 6
- 238000010306 acid treatment Methods 0.000 description 5
- 239000000203 mixture Substances 0.000 description 5
- 229920000642 polymer Polymers 0.000 description 5
- 229920005989 resin Polymers 0.000 description 5
- 239000011347 resin Substances 0.000 description 5
- 230000035945 sensitivity Effects 0.000 description 5
- 238000009987 spinning Methods 0.000 description 5
- 239000002253 acid Substances 0.000 description 4
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 4
- 150000001875 compounds Chemical class 0.000 description 4
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 3
- OFOBLEOULBTSOW-UHFFFAOYSA-N Propanedioic acid Natural products OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 3
- 229910052782 aluminium Inorganic materials 0.000 description 3
- 125000003118 aryl group Chemical group 0.000 description 3
- 239000011230 binding agent Substances 0.000 description 3
- 238000000354 decomposition reaction Methods 0.000 description 3
- 230000002349 favourable effect Effects 0.000 description 3
- 239000011888 foil Substances 0.000 description 3
- 239000007788 liquid Substances 0.000 description 3
- WFKWXMTUELFFGS-UHFFFAOYSA-N tungsten Chemical compound [W] WFKWXMTUELFFGS-UHFFFAOYSA-N 0.000 description 3
- 229910052721 tungsten Inorganic materials 0.000 description 3
- 239000010937 tungsten Substances 0.000 description 3
- 230000000007 visual effect Effects 0.000 description 3
- 238000009941 weaving Methods 0.000 description 3
- VZCYOOQTPOCHFL-OWOJBTEDSA-N Fumaric acid Chemical compound OC(=O)\C=C\C(O)=O VZCYOOQTPOCHFL-OWOJBTEDSA-N 0.000 description 2
- 239000002879 Lewis base Substances 0.000 description 2
- LGRFSURHDFAFJT-UHFFFAOYSA-N Phthalic anhydride Natural products C1=CC=C2C(=O)OC(=O)C2=C1 LGRFSURHDFAFJT-UHFFFAOYSA-N 0.000 description 2
- KKEYFWRCBNTPAC-UHFFFAOYSA-N Terephthalic acid Chemical compound OC(=O)C1=CC=C(C(O)=O)C=C1 KKEYFWRCBNTPAC-UHFFFAOYSA-N 0.000 description 2
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 2
- DZBUGLKDJFMEHC-UHFFFAOYSA-N acridine Chemical compound C1=CC=CC2=CC3=CC=CC=C3N=C21 DZBUGLKDJFMEHC-UHFFFAOYSA-N 0.000 description 2
- 230000004888 barrier function Effects 0.000 description 2
- ISAOCJYIOMOJEB-UHFFFAOYSA-N benzoin Chemical compound C=1C=CC=CC=1C(O)C(=O)C1=CC=CC=C1 ISAOCJYIOMOJEB-UHFFFAOYSA-N 0.000 description 2
- IISBACLAFKSPIT-UHFFFAOYSA-N bisphenol A Chemical compound C=1C=C(O)C=CC=1C(C)(C)C1=CC=C(O)C=C1 IISBACLAFKSPIT-UHFFFAOYSA-N 0.000 description 2
- 229920001577 copolymer Polymers 0.000 description 2
- 230000007547 defect Effects 0.000 description 2
- WOZVHXUHUFLZGK-UHFFFAOYSA-N dimethyl terephthalate Chemical compound COC(=O)C1=CC=C(C(=O)OC)C=C1 WOZVHXUHUFLZGK-UHFFFAOYSA-N 0.000 description 2
- DMBHHRLKUKUOEG-UHFFFAOYSA-N diphenylamine Chemical group C=1C=CC=CC=1NC1=CC=CC=C1 DMBHHRLKUKUOEG-UHFFFAOYSA-N 0.000 description 2
- 239000003822 epoxy resin Substances 0.000 description 2
- 230000004927 fusion Effects 0.000 description 2
- 238000010438 heat treatment Methods 0.000 description 2
- 150000007527 lewis bases Chemical class 0.000 description 2
- 238000002074 melt spinning Methods 0.000 description 2
- TXXHDPDFNKHHGW-UHFFFAOYSA-N muconic acid Chemical compound OC(=O)C=CC=CC(O)=O TXXHDPDFNKHHGW-UHFFFAOYSA-N 0.000 description 2
- 229920000620 organic polymer Polymers 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
- 229920000647 polyepoxide Polymers 0.000 description 2
- 229920000728 polyester Polymers 0.000 description 2
- 239000004848 polyfunctional curative Substances 0.000 description 2
- 238000000859 sublimation Methods 0.000 description 2
- 230000008022 sublimation Effects 0.000 description 2
- 239000000725 suspension Substances 0.000 description 2
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 2
- JNELGWHKGNBSMD-UHFFFAOYSA-N xanthone Chemical compound C1=CC=C2C(=O)C3=CC=CC=C3OC2=C1 JNELGWHKGNBSMD-UHFFFAOYSA-N 0.000 description 2
- PMNMPRXRQYSFRP-UPHRSURJSA-N (z)-2,3-dibromobut-2-enedioic acid Chemical compound OC(=O)C(\Br)=C(\Br)C(O)=O PMNMPRXRQYSFRP-UPHRSURJSA-N 0.000 description 1
- WBYWAXJHAXSJNI-VOTSOKGWSA-M .beta-Phenylacrylic acid Natural products [O-]C(=O)\C=C\C1=CC=CC=C1 WBYWAXJHAXSJNI-VOTSOKGWSA-M 0.000 description 1
- RTNLUFLDZOAXIC-UHFFFAOYSA-N 1,2,3,4,5,6,7,8-octachloronaphthalene Chemical compound ClC1=C(Cl)C(Cl)=C(Cl)C2=C(Cl)C(Cl)=C(Cl)C(Cl)=C21 RTNLUFLDZOAXIC-UHFFFAOYSA-N 0.000 description 1
- RXKOKVQKECXYOT-UHFFFAOYSA-N 1,2,4,5-tetrabromo-3,6-dimethylbenzene Chemical group CC1=C(Br)C(Br)=C(C)C(Br)=C1Br RXKOKVQKECXYOT-UHFFFAOYSA-N 0.000 description 1
- WZCQRUWWHSTZEM-UHFFFAOYSA-N 1,3-phenylenediamine Chemical compound NC1=CC=CC(N)=C1 WZCQRUWWHSTZEM-UHFFFAOYSA-N 0.000 description 1
- AZQWKYJCGOJGHM-UHFFFAOYSA-N 1,4-benzoquinone Chemical compound O=C1C=CC(=O)C=C1 AZQWKYJCGOJGHM-UHFFFAOYSA-N 0.000 description 1
- GQBQDMFMXMUHAA-UHFFFAOYSA-N 1,4-dinitronaphthalene Chemical compound C1=CC=C2C([N+](=O)[O-])=CC=C([N+]([O-])=O)C2=C1 GQBQDMFMXMUHAA-UHFFFAOYSA-N 0.000 description 1
- ZBQZXTBAGBTUAD-UHFFFAOYSA-N 1,5-dichloronaphthalene Chemical compound C1=CC=C2C(Cl)=CC=CC2=C1Cl ZBQZXTBAGBTUAD-UHFFFAOYSA-N 0.000 description 1
- BVEIKFLZWBDLJG-UHFFFAOYSA-N 1-butylanthracene-9,10-dione Chemical class O=C1C2=CC=CC=C2C(=O)C2=C1C=CC=C2CCCC BVEIKFLZWBDLJG-UHFFFAOYSA-N 0.000 description 1
- HJRJRUMKQCMYDL-UHFFFAOYSA-N 1-chloro-2,4,6-trinitrobenzene Chemical compound [O-][N+](=O)C1=CC([N+]([O-])=O)=C(Cl)C([N+]([O-])=O)=C1 HJRJRUMKQCMYDL-UHFFFAOYSA-N 0.000 description 1
- WPMHMYHJGDAHKX-UHFFFAOYSA-N 1-ethenylpyrene Chemical compound C1=C2C(C=C)=CC=C(C=C3)C2=C2C3=CC=CC2=C1 WPMHMYHJGDAHKX-UHFFFAOYSA-N 0.000 description 1
- XFLONXIGNOXKCG-UHFFFAOYSA-N 2,7-dinitroanthracene-9,10-dione Chemical compound C1=C([N+]([O-])=O)C=C2C(=O)C3=CC([N+](=O)[O-])=CC=C3C(=O)C2=C1 XFLONXIGNOXKCG-UHFFFAOYSA-N 0.000 description 1
- KUBDPQJOLOUJRM-UHFFFAOYSA-N 2-(chloromethyl)oxirane;4-[2-(4-hydroxyphenyl)propan-2-yl]phenol Chemical compound ClCC1CO1.C=1C=C(O)C=CC=1C(C)(C)C1=CC=C(O)C=C1 KUBDPQJOLOUJRM-UHFFFAOYSA-N 0.000 description 1
- XUGNJOCQALIQFG-UHFFFAOYSA-N 2-ethenylquinoline Chemical compound C1=CC=CC2=NC(C=C)=CC=C21 XUGNJOCQALIQFG-UHFFFAOYSA-N 0.000 description 1
- KXYAVSFOJVUIHT-UHFFFAOYSA-N 2-vinylnaphthalene Chemical compound C1=CC=CC2=CC(C=C)=CC=C21 KXYAVSFOJVUIHT-UHFFFAOYSA-N 0.000 description 1
- LWFUFLREGJMOIZ-UHFFFAOYSA-N 3,5-dinitrosalicylic acid Chemical compound OC(=O)C1=CC([N+]([O-])=O)=CC([N+]([O-])=O)=C1O LWFUFLREGJMOIZ-UHFFFAOYSA-N 0.000 description 1
- IARXLBTXILYASE-UHFFFAOYSA-N 3,6-dinitro-9h-carbazole Chemical compound C1=C([N+]([O-])=O)C=C2C3=CC([N+](=O)[O-])=CC=C3NC2=C1 IARXLBTXILYASE-UHFFFAOYSA-N 0.000 description 1
- RBTBFTRPCNLSDE-UHFFFAOYSA-N 3,7-bis(dimethylamino)phenothiazin-5-ium Chemical compound C1=CC(N(C)C)=CC2=[S+]C3=CC(N(C)C)=CC=C3N=C21 RBTBFTRPCNLSDE-UHFFFAOYSA-N 0.000 description 1
- MOMUQFPOZNRJCZ-UHFFFAOYSA-N 3-chloro-9-ethenylcarbazole Chemical compound C1=CC=C2C3=CC(Cl)=CC=C3N(C=C)C2=C1 MOMUQFPOZNRJCZ-UHFFFAOYSA-N 0.000 description 1
- FKDIWXZNKAZCBY-UHFFFAOYSA-N 9,10-dichloroanthracene Chemical compound C1=CC=C2C(Cl)=C(C=CC=C3)C3=C(Cl)C2=C1 FKDIWXZNKAZCBY-UHFFFAOYSA-N 0.000 description 1
- LSIKFJXEYJIZNB-UHFFFAOYSA-N 9-Nitroanthracene Chemical compound C1=CC=C2C([N+](=O)[O-])=C(C=CC=C3)C3=CC2=C1 LSIKFJXEYJIZNB-UHFFFAOYSA-N 0.000 description 1
- ZIRVQSRSPDUEOJ-UHFFFAOYSA-N 9-bromoanthracene Chemical compound C1=CC=C2C(Br)=C(C=CC=C3)C3=CC2=C1 ZIRVQSRSPDUEOJ-UHFFFAOYSA-N 0.000 description 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 1
- WBYWAXJHAXSJNI-SREVYHEPSA-N Cinnamic acid Chemical compound OC(=O)\C=C/C1=CC=CC=C1 WBYWAXJHAXSJNI-SREVYHEPSA-N 0.000 description 1
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 1
- JIGUQPWFLRLWPJ-UHFFFAOYSA-N Ethyl acrylate Chemical compound CCOC(=O)C=C JIGUQPWFLRLWPJ-UHFFFAOYSA-N 0.000 description 1
- 229920000877 Melamine resin Polymers 0.000 description 1
- TXXHDPDFNKHHGW-CCAGOZQPSA-N Muconic acid Natural products OC(=O)\C=C/C=C\C(O)=O TXXHDPDFNKHHGW-CCAGOZQPSA-N 0.000 description 1
- QLZHNIAADXEJJP-UHFFFAOYSA-N Phenylphosphonic acid Chemical class OP(O)(=O)C1=CC=CC=C1 QLZHNIAADXEJJP-UHFFFAOYSA-N 0.000 description 1
- 239000004693 Polybenzimidazole Substances 0.000 description 1
- 239000004642 Polyimide Substances 0.000 description 1
- 239000004793 Polystyrene Substances 0.000 description 1
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 description 1
- 244000028419 Styrax benzoin Species 0.000 description 1
- 235000000126 Styrax benzoin Nutrition 0.000 description 1
- 235000008411 Sumatra benzointree Nutrition 0.000 description 1
- UATJOMSPNYCXIX-UHFFFAOYSA-N Trinitrobenzene Chemical compound [O-][N+](=O)C1=CC([N+]([O-])=O)=CC([N+]([O-])=O)=C1 UATJOMSPNYCXIX-UHFFFAOYSA-N 0.000 description 1
- JSQFXMIMWAKJQJ-UHFFFAOYSA-N [9-(2-carboxyphenyl)-6-(ethylamino)xanthen-3-ylidene]-diethylazanium;chloride Chemical compound [Cl-].C=12C=CC(=[N+](CC)CC)C=C2OC2=CC(NCC)=CC=C2C=1C1=CC=CC=C1C(O)=O JSQFXMIMWAKJQJ-UHFFFAOYSA-N 0.000 description 1
- 238000000862 absorption spectrum Methods 0.000 description 1
- QLDHWVVRQCGZLE-UHFFFAOYSA-N acetyl cyanide Chemical compound CC(=O)C#N QLDHWVVRQCGZLE-UHFFFAOYSA-N 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- BGLGAKMTYHWWKW-UHFFFAOYSA-N acridine yellow Chemical compound [H+].[Cl-].CC1=C(N)C=C2N=C(C=C(C(C)=C3)N)C3=CC2=C1 BGLGAKMTYHWWKW-UHFFFAOYSA-N 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- RGCKGOZRHPZPFP-UHFFFAOYSA-N alizarin Chemical compound C1=CC=C2C(=O)C3=C(O)C(O)=CC=C3C(=O)C2=C1 RGCKGOZRHPZPFP-UHFFFAOYSA-N 0.000 description 1
- 150000008064 anhydrides Chemical class 0.000 description 1
- KEQZHLAEKAVZLY-UHFFFAOYSA-N anthracene-9-carbonitrile Chemical compound C1=CC=C2C(C#N)=C(C=CC=C3)C3=CC2=C1 KEQZHLAEKAVZLY-UHFFFAOYSA-N 0.000 description 1
- PYKYMHQGRFAEBM-UHFFFAOYSA-N anthraquinone Natural products CCC(=O)c1c(O)c2C(=O)C3C(C=CC=C3O)C(=O)c2cc1CC(=O)OC PYKYMHQGRFAEBM-UHFFFAOYSA-N 0.000 description 1
- 150000004056 anthraquinones Chemical class 0.000 description 1
- 239000004760 aramid Substances 0.000 description 1
- 229920003235 aromatic polyamide Polymers 0.000 description 1
- WURBFLDFSFBTLW-UHFFFAOYSA-N benzil Chemical compound C=1C=CC=CC=1C(=O)C(=O)C1=CC=CC=C1 WURBFLDFSFBTLW-UHFFFAOYSA-N 0.000 description 1
- LHMRXAIRPKSGDE-UHFFFAOYSA-N benzo[a]anthracene-7,12-dione Chemical compound C1=CC2=CC=CC=C2C2=C1C(=O)C1=CC=CC=C1C2=O LHMRXAIRPKSGDE-UHFFFAOYSA-N 0.000 description 1
- 229960002130 benzoin Drugs 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- JHIWVOJDXOSYLW-UHFFFAOYSA-N butyl 2,2-difluorocyclopropane-1-carboxylate Chemical compound CCCCOC(=O)C1CC1(F)F JHIWVOJDXOSYLW-UHFFFAOYSA-N 0.000 description 1
- 150000001244 carboxylic acid anhydrides Chemical class 0.000 description 1
- VYXSBFYARXAAKO-WTKGSRSZSA-N chembl402140 Chemical compound Cl.C1=2C=C(C)C(NCC)=CC=2OC2=C\C(=N/CC)C(C)=CC2=C1C1=CC=CC=C1C(=O)OCC VYXSBFYARXAAKO-WTKGSRSZSA-N 0.000 description 1
- 229930016911 cinnamic acid Natural products 0.000 description 1
- 235000013985 cinnamic acid Nutrition 0.000 description 1
- 230000001112 coagulating effect Effects 0.000 description 1
- 239000000470 constituent Substances 0.000 description 1
- 238000007334 copolymerization reaction Methods 0.000 description 1
- 239000013078 crystal Substances 0.000 description 1
- 230000006866 deterioration Effects 0.000 description 1
- 230000001627 detrimental effect Effects 0.000 description 1
- 150000005690 diesters Chemical class 0.000 description 1
- PAYWCKGMOYQZAW-UHFFFAOYSA-N dimethyl 2-nitrobenzene-1,4-dicarboxylate Chemical compound COC(=O)C1=CC=C(C(=O)OC)C([N+]([O-])=O)=C1 PAYWCKGMOYQZAW-UHFFFAOYSA-N 0.000 description 1
- GMSCBRSQMRDRCD-UHFFFAOYSA-N dodecyl 2-methylprop-2-enoate Chemical compound CCCCCCCCCCCCOC(=O)C(C)=C GMSCBRSQMRDRCD-UHFFFAOYSA-N 0.000 description 1
- 238000000578 dry spinning Methods 0.000 description 1
- IINNWAYUJNWZRM-UHFFFAOYSA-L erythrosin B Chemical compound [Na+].[Na+].[O-]C(=O)C1=CC=CC=C1C1=C2C=C(I)C(=O)C(I)=C2OC2=C(I)C([O-])=C(I)C=C21 IINNWAYUJNWZRM-UHFFFAOYSA-L 0.000 description 1
- 229940011411 erythrosine Drugs 0.000 description 1
- 235000012732 erythrosine Nutrition 0.000 description 1
- 239000004174 erythrosine Substances 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- AIJZIRPGCQPZSL-UHFFFAOYSA-N ethylenetetracarboxylic acid Chemical compound OC(=O)C(C(O)=O)=C(C(O)=O)C(O)=O AIJZIRPGCQPZSL-UHFFFAOYSA-N 0.000 description 1
- 239000001530 fumaric acid Substances 0.000 description 1
- 235000019382 gum benzoic Nutrition 0.000 description 1
- 150000002366 halogen compounds Chemical class 0.000 description 1
- LNEPOXFFQSENCJ-UHFFFAOYSA-N haloperidol Chemical compound C1CC(O)(C=2C=CC(Cl)=CC=2)CCN1CCCC(=O)C1=CC=C(F)C=C1 LNEPOXFFQSENCJ-UHFFFAOYSA-N 0.000 description 1
- 238000013007 heat curing Methods 0.000 description 1
- 125000000623 heterocyclic group Chemical group 0.000 description 1
- 125000000468 ketone group Chemical group 0.000 description 1
- 229940018564 m-phenylenediamine Drugs 0.000 description 1
- 229940107698 malachite green Drugs 0.000 description 1
- FDZZZRQASAIRJF-UHFFFAOYSA-M malachite green Chemical compound [Cl-].C1=CC(N(C)C)=CC=C1C(C=1C=CC=CC=1)=C1C=CC(=[N+](C)C)C=C1 FDZZZRQASAIRJF-UHFFFAOYSA-M 0.000 description 1
- 229940002712 malachite green oxalate Drugs 0.000 description 1
- VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 description 1
- 239000011976 maleic acid Substances 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- PHOYNPDEAQEHQR-UHFFFAOYSA-N methyl anthracene-9-carboxylate Chemical compound C1=CC=C2C(C(=O)OC)=C(C=CC=C3)C3=CC2=C1 PHOYNPDEAQEHQR-UHFFFAOYSA-N 0.000 description 1
- WBYWAXJHAXSJNI-UHFFFAOYSA-N methyl p-hydroxycinnamate Natural products OC(=O)C=CC1=CC=CC=C1 WBYWAXJHAXSJNI-UHFFFAOYSA-N 0.000 description 1
- 229960000907 methylthioninium chloride Drugs 0.000 description 1
- 125000004108 n-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- KKFHAJHLJHVUDM-UHFFFAOYSA-N n-vinylcarbazole Chemical compound C1=CC=C2N(C=C)C3=CC=CC=C3C2=C1 KKFHAJHLJHVUDM-UHFFFAOYSA-N 0.000 description 1
- ZNPWYAMBOPRTHW-UHFFFAOYSA-N naphthalene-1,2-dicarbonitrile Chemical compound C1=CC=CC2=C(C#N)C(C#N)=CC=C21 ZNPWYAMBOPRTHW-UHFFFAOYSA-N 0.000 description 1
- 150000002828 nitro derivatives Chemical class 0.000 description 1
- PNJWIWWMYCMZRO-UHFFFAOYSA-N pent‐4‐en‐2‐one Natural products CC(=O)CC=C PNJWIWWMYCMZRO-UHFFFAOYSA-N 0.000 description 1
- 239000012466 permeate Substances 0.000 description 1
- 229920001568 phenolic resin Polymers 0.000 description 1
- 230000002165 photosensitisation Effects 0.000 description 1
- 239000003504 photosensitizing agent Substances 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- OXNIZHLAWKMVMX-UHFFFAOYSA-N picric acid Chemical compound OC1=C([N+]([O-])=O)C=C([N+]([O-])=O)C=C1[N+]([O-])=O OXNIZHLAWKMVMX-UHFFFAOYSA-N 0.000 description 1
- 239000004014 plasticizer Substances 0.000 description 1
- 229920002006 poly(N-vinylimidazole) polymer Polymers 0.000 description 1
- 229920002480 polybenzimidazole Polymers 0.000 description 1
- 229920002577 polybenzoxazole Polymers 0.000 description 1
- 229920000515 polycarbonate Polymers 0.000 description 1
- 239000004417 polycarbonate Substances 0.000 description 1
- 229920000139 polyethylene terephthalate Polymers 0.000 description 1
- 239000005020 polyethylene terephthalate Substances 0.000 description 1
- 229920001721 polyimide Polymers 0.000 description 1
- 238000006116 polymerization reaction Methods 0.000 description 1
- 229920002223 polystyrene Polymers 0.000 description 1
- 229920002635 polyurethane Polymers 0.000 description 1
- 239000004814 polyurethane Substances 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 150000004053 quinones Chemical class 0.000 description 1
- PYWVYCXTNDRMGF-UHFFFAOYSA-N rhodamine B Chemical compound [Cl-].C=12C=CC(=[N+](CC)CC)C=C2OC2=CC(N(CC)CC)=CC=C2C=1C1=CC=CC=C1C(O)=O PYWVYCXTNDRMGF-UHFFFAOYSA-N 0.000 description 1
- 229940043267 rhodamine b Drugs 0.000 description 1
- 229910052710 silicon Inorganic materials 0.000 description 1
- 239000010703 silicon Substances 0.000 description 1
- 238000004513 sizing Methods 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- UGNWTBMOAKPKBL-UHFFFAOYSA-N tetrachloro-1,4-benzoquinone Chemical compound ClC1=C(Cl)C(=O)C(Cl)=C(Cl)C1=O UGNWTBMOAKPKBL-UHFFFAOYSA-N 0.000 description 1
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 1
- JBWKIWSBJXDJDT-UHFFFAOYSA-N triphenylmethyl chloride Chemical compound C=1C=CC=CC=1C(C=1C=CC=CC=1)(Cl)C1=CC=CC=C1 JBWKIWSBJXDJDT-UHFFFAOYSA-N 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 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
- G03G5/09—Sensitisors or activators, e.g. dyestuffs
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
- D06M23/00—Treatment of fibres, threads, yarns, fabrics or fibrous goods made from such materials, characterised by the process
-
- 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
-
- 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
- G03G5/07—Polymeric photoconductive materials
Definitions
- a photoconductive fiber sheet is produced by dyeing with a sensitizing coloring matter a fiber sheet made of organic high polymer fibers capable of acting as a Lewis base against a Lewis acid and forming a charge transfer complex with the Lewis acid and then treating the fiber sheet with the Lewis acid.
- This invention relates to a process for preparing a photoconductive fiber sheet which fulfills multipurpose applications.
- Conventional electrophotographic photosensitive members generally comprise a supporting body and a photconductive layer laid thereon, in which the photoconductive layer consists either solely of a photoconductive substance or of a photoconductive substance and a binder resin. Therefore, to prepare the photosensitive member, a photoconductive substance or, when required, a mixture of the photoconductive substance and a binder resin was coated on one surface of a support such as a metal plate, paper, etc. by an ordinary layer forming method.
- a support such as a metal plate, paper, etc.
- the solution or suspension system which mainly contains the photoconductive substance, permeates into the supporting body.
- the photoconductive layer has a weak mechanical strength. These factors have caused the photosensitive member to have a short service life and a low sensitivity to light.
- peeling of the photoconductive layer is often caused by external force or, due to nonuniformity in adhesiveness, partial unevenness in photosensitivity is produced which results in the so-called fog.
- the thickness of the photoconductive layer becomes substantially uneven and consequently gives a photosensitive member which has a partially different dark resistance. This also results in the drop of photosensitivity. Still further, since the mechanical strength of the above-mentioned photoconductive layer is generally weak and its surface is easily damaged by the repeated rubbing when the layer is used in the electrophotographic copying process, the service life of the photosensitive member is reduced remarkably.
- the first purpose of this invention is to offer a process by which the still insufiicient practicality of organic photoconductive bodies can be drastically increased.
- the sensitizing agents used are usually assigned with a heavy limitation.
- the organic photoconductive materials to be made in a fiber form are usually polymers, selection of soluble and insoluble solvents is normally a very diflicult matter and, for this reason, the wet spinning method has limitation in its function. As a result, iits not an easy task to obtain an optimum combination of organic photoconductive material and sensitizing agent in the wet spinning method. Further, a wet spinning method can not be applied to some materials. In addition, in almost all wet spinning processes a heat curing is essential at the final stage so that the use of sensitizing agents encounters a difiiculty as in the case of the melt spinning method.
- Another object of this invention is to offer an extremely economical process for preparing a photoconductive fiber sheet by improving the conventional photoconductive fiber sheet forming technique, by assuring a high photoconductivity, and by admitting a free selective use of sensitizing agent, etc.
- a further object of this invention is to ofler a process for preparing a photoconductive fiber sheet having an excellent performance in multicolor reproduction process.
- a still further object of this invention is to offer a process for preparing a photoconductive fiber sheet in which the photoconductivity is given in the form of a pattern.
- This invention relates to a process for preparing a photoconductive fiber sheet which comprises dyeing a fiber sheet made of an organic high polymer material as the main material with a sensitizing coloring matter and then treating it with Lewis acid.
- the organic high polymer material is a substance which has the property of assuming the property of a Lewis base against the Lewis acid and forming with it a charge transfer complex.
- the fiber sheet is a paper or cloth made or woven from fibers composed of an organic high polymer material.
- the technical feature of this invention may be explained by two factors. One is to dye the fiber sheet with a sensitizing coloring matter and the other is the joint use of a sensitizing coloring matter and a Lewis acid as the sensitizing agent.
- the greatest feature of this invention is that quite an excellent sensitizing effect for the photoconductivity of the sheet is obtained by treating the fiber sheet with a sensitizing coloring matter and by further treating it with a Lewis acid.
- the dyeing step can be effected on the sheet after it is formed, it is not required to choose a particular kind of high polymer material and a spinning method in order to prepare a fiber sheet. In other words, it is possible to form a fiber sheet by using a most desired material with a most suitable method.
- the sensitivity of the fiber sheet dyed in such a way is increased remarkably by treating it With a Lewis acid.
- the characteristics of the photoconductive fiber sheet obtained according to the present invention are remarkably excellent as compared with those of conventional photoconductive fiber sheets obtained by adding a sensitizing agent preliminarily.
- the photoconductive fiber sheet is free from various disadvantages such as loss of the sensitizing agent caused by decomposition or sublimation, and lowering of photosensitivity caused by detrimental substance produced by decomposition. Therefore, the sensitivity of the photoconductive fiber can be increased to a practical level.
- the sensitizing agent particularly a Lewis acid, is liable to cause deterioration of the physical property of the fiber itself during the melt spinning process while in the present invention the sensitizing agent is not present in the spinning process.
- the sensitizing agent is uniformly absorbed to the fiber in an appropriate amount.
- organic polymers which form the fiber sheet Polymers having aromatic rings or heterocyclic rings such as polyethylene terephthalate, polyester of bisphenol A and terephthalic acid, polyester of 9-ethylcarbazole-3,6-dibutanic acid and ethylene glycol, aromatic polyamides, polydiphenylene oxide, polybenzimidazole,
- polybenzoxazole give favorable results in this invention.
- Other polymers that can be used in this invention are: Phenolformaldehyde resins, epoxy resins, polycarbonates, melamine resins, polyimides, polyurethanes, aromatic silicon resins, polystyrene, poly (2-vinyl quinoline), poly-(3, 3-dimethyl-diphenylene-4,4), polyvinylxylene, poly (2- vinyl-naphthalene), polyindene, polyvinylimidazole, poly (3-vinyl-pyrene).
- Lewis acids As representative examples of Lewis acids, the following compounds give very favorable results: Anthraquinone-B-carboxylic acid ester, anthraquinone-fi-carboxylic acid-sec-amyl ester, Z-nitrofiuorenoncarboxylic acid-n-butyl ester, and anthraquinone-fl-carboxylic acid-n-butyl ester. Furthermore, the following compounds may be used:
- Nitro compounds such as 1,3,5-trinitrobenzene, picric acid, picryl chloride, 3,5-dinitrosalicylic acid, 1,4-dinitronaphthalene, 9-nitro-anthracene, 2,7-dinitroanthraquinone, 3,6-dinitrocarbazole, and S-nitrobarbitalic acid.
- Cyanic compounds such as acetic cyanide, tetracyanethylene, dicyanonaphthalene, and 9-cyano-anthracene.
- Acids such as acetodicarboxylic acid, fumaric acid, maleic acid, dibromomaleic acid, malonic acid, muconic acid, phthalic acid, cinnamic acid, and phenylphosphonic acid derivatives.
- Carboxylic anhydrides such as phthalic anhydride, tetra halogenated phthalic anhydride, hexabromonaphthalie anhydride, and chrycene-2,4,8,9-tetracarboxylic anhydride.
- Esters such as ethylenetetracarboxylic acid tetraethyl acetylester, terephthalic acid dimethylester, nitroterephthalic acid dimethylester, phthalic diester, and anthracene-9-carboxylic methylester.
- Halogen compounds such as 1,5-dichloronaphthalene, tetrabromo-p-xylene, triphenylchloromethane, octachloronaphthalene, 9-bromo-anthracene, and 9,10-dichloroanthracene.
- Quinones such as benzoquinone, l,4-naphthoquinone, anthraquinone, 1,2-benzanthraquinone, aromatic 1,2-quinones, and chloranil.
- Keto compounds such as pyrene-B-aldehyde, benzil, benzoin, 2-nitroindandione-1,3, 9-propyonylanthracene, and xanthone.
- A20 compounds such as acridine, azophenanthrene, and l-azo-pyrene.
- the sensitizing coloring matters used in this invention are common spectrum sensitizers and are not limited by any other conditions.
- Some of the examples of sensitizing coloring matter other than those disclosed in the examples shown later are Rhodamine B, Malachite Green Chloride, Crystal Violet, Rhodamine G extra. Malachite Green Oxalate, Rose Bengal, Erythrosine, Alizarin Red, Brilliant Green, Rhodamine 6G, Methylene Blue, and Acridine Yellow.
- a sheet can be formed by employing an ordinary paper making or spinning process.
- a typical process comprises firstly dissolving or, in particular cases, suspending the source material for sheet forming in an appropriate solvent, agitating, adding a hardener or softener, when required, and, in the case of dry spinning, the resulting solution is ejected through a spinnerette and then the solvent is evaporated by means of hot air to form a fiber.
- the solution is ejected through the spinnerette, and introduced to a coagulating solution to form a fiber. The fiber thus made is beaten and then made into paper, or the above-mentioned fiber is woven into cloth to form a sheet.
- the sheet may be formed optionally by employing a hitherto known method. It is also allowed to add various kinds of additives such as sizing agents, electric resistance controlling agents, plasticizers, and other resins in order to make the property of the sheet more favorable.
- the dyeing of the fiber sheet with sensitizing coloring matter is effected by using under such conditions as heating a solution prepared by dissolving or dispersing the sensitizing coloring matter in an appropriate solvent. In this invention, it is particularly preferable and simple to carry out the dyeing simultaneously with the treatment with a Lewis acid. When treatment with the Lewis acid is effected separately, it is preferable to dissolve the Lewis acid in an appropriate solvent in which the sheet is not soluble and treat the sheet with the resulting Lewis acid solution. However, when the Lewis acid in its normal state is in a liquid form, the acid can be used as it is.
- the sheet is preferably required to have an affinity to the Lewis acid solution or liquid Lewis acid sufiicient to wet the surface of the sheet and some degree of hygroscopicity.
- the dyeing treatment and Lewis acid treatment are carried out after forming a fiber sheet. Therefore, this invention is, of course, applicable to any desirable combination of an organic polymer for forming a fiber sheet, sensitizing coloring matter, and Lewis acid.
- the fiber sheet is only a material in this invention, and the actual photoconductive fiber sheet can be formed by treating the material normally only once. This enables various kinds of sheets to be made freely and very economically.
- the photoconductive fiber sheet is obtained by using two or more kinds of sensitizing coloring matters so as to impart a panchromatic photosensitivity over the visual spectrum wavelength region to offer a photosensitive sheet which is suited to forming color copy image.
- the fiber in the stage previous to the fiber sheet is divided, for example, into three blocks. Each block is dyed separately with a sensitizing coloring matter so as to impart a photosensitive wavelength characteristic corresponding to red, blue and green (Lewis acid treatment may be carried out during this step), and then the same quantity of the fibers having the above-mentioned different photosensitive wavelength characteristics respectively is collected together to be woven into cloth.
- the photoconductive fiber sheet thus obtained can also offer a photosensitive sheet suitable for color copy image formation.
- a photoconductive fiber sheet having sensitized photoconductive patterns by first dyeing the fiber sheet with a sensitizing coloring matter and then treating it with Lewis acid in such a way that the treated portion forms a pattern during treatment.
- the photoconductive fiber sheet offers a photosensitive sheet capable of accepting electrostatic printing as shown in the example described later. Examples of this invention are given below. It should be understood, however, that these are given for illustrating this invention, but not for limiting this invention.
- Dye bath [I] Methanol solution containing a sensitizing coloring matter which afi'ords photosensitive wavelength characteristic mainly corresponding to blue spectrum and a Lewis acid.
- the Lewis acid is anthraquinone-fi-carboxylic acid-n-butylester (the same compound is used in the dye baths [II] and [III]) and the sensitizing coloring matter is a substance represented by the following structural formula.
- Dye bath [II] Methanol solution containing a sensitizing coloring matter affording photosensitive wavelength characteristic mainly corresponding to red spectrum and the Lewis acid as used in dye bath [I].
- the sensitizing coloring matter is diphenylamine blue.
- Dye bath [III] Methanol solution containing a sensitizing coloring matter affording photosensitive wavelength characteristic mainly corresponding to green spectrum and the Lewis acid as used in dye bath [I].
- the above-mentioned fiber was divided into 3 equal groups. One of the groups was subjected to treatment with the dye bath [1], the second group with the dye bath [II], and the remaining group with the dye bath [III] and each was treated with the Lewis acid simultaneously with the dyeing. In this way, 3 kinds of fibers having photosensitive wavelength characteristics corresponding to blue, red, and green, respectively were prepared. These fibers were mixed and woven into cloth by an ordinary method.
- EXAMPLE 2 A copolymer of 3-chloro-9-vinylcarbazole and ethyl acrylate (polymerization molecular ratio :15) was melted and spun at about 270 C. and the resulting fiber was woven into cloth. The cloth was subjected to treatment with the mixture of dye baths [I], [II], and [III] of Example 3 to produce a photoconductive cloth. Then, the cloth thus produced was used for reproduction under the same conditions as in Example 3. A clear color image was obtained was an exposure time of 2.5 seconds.
- EXAMPLE 3 45 g. of Epikote 1001 (Trade name, supplied by Shell Petroleum Co., epoxy resin) and 0.8 g. of resin hardener, m-phenylenediamine were dissolved in ml. of tetrahydrofuran. The resulting solution was injected into water at a rate of 20 ml. per second with stirring to separate the fine fibers in a rather lump form. The fine fibers were then collected and made into paper of about 5 ,u in thickness, final heating being at 100 C. for 10 minutes. The surface of the paper was treated with a mixture of the dye baths [1], [II] and [III] used in Example 1, dyed with sensitizing coloring matters and then treated with a Lewis acid.
- Epikote 1001 Trade name, supplied by Shell Petroleum Co., epoxy resin
- resin hardener 0.8 g. of resin hardener, m-phenylenediamine
- the paper thus prepared was charged by a charging device to which was applied a high voltage of about 5.5 kv. to obtain a uniform negative charge of about 1,000 v. on the electrostatic image forming surface.
- a positive original film was laid on the above-mentioned paper in close contact and, by an exposure device having a watt tungsten lamp as a light source was placed at 10 cm. away from the film, an exposure was made for about 4 seconds.
- the film was then developed by dipping it into a positive liquid developer. A good positive image with fidelity to the original was obtained.
- the above-mentioned paper was first subjected to a dyeing process by means of a dye bath containing only the sensitizing coloring matter, instead of a simultaneous application of the dyeing process and the Lewis acid process, and next subjected to the Lewis acid processing and, in this Lewis acid processing, a piece of aluminum foil cut into a pattern form was laid on the surface of the paper in close contact and then a Lewis acid (anthraquinone-fl-carboxylic acid-n-butylester) solution was applied to the paper covered with the aluminum foil.
- a Lewis acid anthraquinone-fl-carboxylic acid-n-butylester
- this paper was charged under the same condition as above followed by whole surface exposure made by the exposure device having a 150 w. tungsten lamp as the light source for about 3.5 seconds at a distance of 100 cm.
- the paper was then developed by a magnet brush method using a positively charged toner, and fixed by heat. As a result, a clear negative image which followed the pattern was obtained.
- the photoconductive paper that followed the above-mentioned pattern was wound around an aluminum metal drum, and visual image obtained by conducting the above-mentioned charging, whole surface exposure and development was subjected to copy image forming process which transfers the image to paper. It was found that a clear pattern image was allowed to be transferred to the paper more than 5000 times.
- a process for preparing a photoconductive fiber sheet which comprises preparing a fiber sheet comprising an organic high polymer material; treating said sheet with a Lewis acid capable of reacting with said material to form a photoconductive charge transfer complex and dyeing said sheet with a spectral sensitizing coloring matter.
- the spectral sensitizing coloring matter is a mixture of two or more coloring matters having different absorption spectrum characteristics so as to impart a panchromatic photosensitive property for the visual spectrum wavelength region to the fiber sheet.
- the photosensitizing coloring matter is a mixture of a spectral sensitizing coloring matter capable of imparting to the fiber sheet a photosensitive wavelength characteristic mainly corresponding to red spectrum, a spectral sensitizing coloring matter capable of imparting to the fiber sheet a photosensitive wavelength characteristic mainly corresponding to blue spectrum, and a spectral sensitizing coloring matter capable of imparting to the fiber sheet a photosensitive wavelength characteristic mainly corresponding to green spectrum.
- a process for preparing a photoconductive fiber sheet which comprises preparing a fiber sheet comprising an organic high polymer material, treating said sheet with a Lewis acid capable of reacting with said material to form a photoconductive charge transfer complex and dyeing said sheet with a spectral sensitizing coloring matter wherein the treatment with the Lewis acid is carried out in such a manner that the region treated with said Lewis acid forms a photoconductive pattern capable of accepting electrostatic printing.
Landscapes
- Physics & Mathematics (AREA)
- General Physics & Mathematics (AREA)
- Engineering & Computer Science (AREA)
- Textile Engineering (AREA)
- Photoreceptors In Electrophotography (AREA)
- Coloring (AREA)
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP44052266A JPS4823452B1 (enrdf_load_stackoverflow) | 1969-07-02 | 1969-07-02 |
Publications (1)
Publication Number | Publication Date |
---|---|
US3708294A true US3708294A (en) | 1973-01-02 |
Family
ID=12909952
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US00050899A Expired - Lifetime US3708294A (en) | 1969-07-02 | 1970-06-29 | Process for preparing a photoconductive fiber sheet |
Country Status (4)
Country | Link |
---|---|
US (1) | US3708294A (enrdf_load_stackoverflow) |
JP (1) | JPS4823452B1 (enrdf_load_stackoverflow) |
DE (1) | DE2032656A1 (enrdf_load_stackoverflow) |
GB (1) | GB1317013A (enrdf_load_stackoverflow) |
Families Citing this family (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS55145650U (enrdf_load_stackoverflow) * | 1979-04-06 | 1980-10-20 | ||
JPS56174549U (enrdf_load_stackoverflow) * | 1980-05-28 | 1981-12-23 |
-
1969
- 1969-07-02 JP JP44052266A patent/JPS4823452B1/ja active Pending
-
1970
- 1970-06-29 US US00050899A patent/US3708294A/en not_active Expired - Lifetime
- 1970-06-30 GB GB3165670A patent/GB1317013A/en not_active Expired
- 1970-07-01 DE DE19702032656 patent/DE2032656A1/de active Granted
Also Published As
Publication number | Publication date |
---|---|
GB1317013A (en) | 1973-05-16 |
DE2032656B2 (enrdf_load_stackoverflow) | 1974-03-28 |
JPS4823452B1 (enrdf_load_stackoverflow) | 1973-07-13 |
DE2032656C3 (enrdf_load_stackoverflow) | 1974-10-31 |
DE2032656A1 (de) | 1971-01-28 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
US3155503A (en) | Electrophotographic material | |
US3287123A (en) | Process for the sensitization of photoconductors | |
US3159483A (en) | Process for the preparation of electrophotographic reversed images | |
US4388392A (en) | Laminated photosensitive plate for electrophotography having an electron donative polymer and phenanthrene charge transport layer | |
US3488705A (en) | Thermally unstable organic acid salts of triarylmethane dyes as sensitizers for organic photoconductors | |
JPS61109056A (ja) | 積層型電子写真感光体 | |
US3287120A (en) | Process for the sensitization of photoconductors | |
JPS609259B2 (ja) | 電子写真用感光材料 | |
US4284698A (en) | Layered electrophotographic photoconductor | |
US3890146A (en) | Organic photoconductive materials derived from reacting a photoconductive compound with a color compound | |
US3933664A (en) | Organic photoconductive toner materials | |
US3708294A (en) | Process for preparing a photoconductive fiber sheet | |
US3287114A (en) | Process for the sensitization of photoconductors | |
US3287119A (en) | Process for the sensitization of photoconductors | |
US3448028A (en) | N-substituted - 8,13-dioxodinaphtho (2,1-b; 2',3'-d)-furan - 6 - carboxamides as electrically photosensitive materials in electrophotographic processes | |
US3169060A (en) | Photoconductive layers for electrophotographic purposes | |
JPS6251462B2 (enrdf_load_stackoverflow) | ||
EP0089603A1 (de) | Elektrophotographisches Aufzeichnungsmaterial | |
JPS5962861A (ja) | 電子写真用感光体 | |
US3984378A (en) | Process for manufacturing nitropyrene-formaldehyde resin | |
US3287115A (en) | Process for the sensitization of photoconductors | |
US3287116A (en) | Process for the sensitization of photoconductors | |
US3287113A (en) | Process for the sensitization of photoconductors | |
JPS6239585A (ja) | 光導電性組成物用テルラン系増感剤 | |
US5248579A (en) | Electrophotographic recording material |