JPS6334571A - Copying method - Google Patents
Copying methodInfo
- Publication number
- JPS6334571A JPS6334571A JP61177759A JP17775986A JPS6334571A JP S6334571 A JPS6334571 A JP S6334571A JP 61177759 A JP61177759 A JP 61177759A JP 17775986 A JP17775986 A JP 17775986A JP S6334571 A JPS6334571 A JP S6334571A
- Authority
- JP
- Japan
- Prior art keywords
- image
- toner
- depth
- intermediate transfer
- transfer medium
- 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.)
- Pending
Links
- 238000000034 method Methods 0.000 title claims description 49
- 238000012546 transfer Methods 0.000 claims abstract description 82
- 230000003746 surface roughness Effects 0.000 claims abstract description 10
- 238000010438 heat treatment Methods 0.000 claims abstract description 7
- 238000011161 development Methods 0.000 abstract description 7
- 238000003825 pressing Methods 0.000 abstract description 3
- 229920001577 copolymer Polymers 0.000 description 30
- 239000000543 intermediate Substances 0.000 description 29
- 108091008695 photoreceptors Proteins 0.000 description 25
- 229920005989 resin Polymers 0.000 description 18
- 239000011347 resin Substances 0.000 description 18
- 150000001336 alkenes Chemical class 0.000 description 16
- 230000005291 magnetic effect Effects 0.000 description 14
- 239000000178 monomer Substances 0.000 description 13
- 239000000463 material Substances 0.000 description 12
- -1 polytetrafluoroethylene Polymers 0.000 description 12
- 235000014113 dietary fatty acids Nutrition 0.000 description 11
- 239000000194 fatty acid Substances 0.000 description 11
- 229930195729 fatty acid Natural products 0.000 description 11
- 239000002245 particle Substances 0.000 description 11
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 10
- 239000003795 chemical substances by application Substances 0.000 description 9
- 150000004665 fatty acids Chemical class 0.000 description 9
- 239000010410 layer Substances 0.000 description 9
- 150000001408 amides Chemical class 0.000 description 8
- 229910052751 metal Inorganic materials 0.000 description 8
- 239000002184 metal Substances 0.000 description 8
- 229920000098 polyolefin Polymers 0.000 description 8
- 229920006015 heat resistant resin Polymers 0.000 description 7
- JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 description 7
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 7
- 229920002554 vinyl polymer Polymers 0.000 description 7
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical class [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 6
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- 239000000203 mixture Substances 0.000 description 6
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- 238000004140 cleaning Methods 0.000 description 5
- 239000003086 colorant Substances 0.000 description 5
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- 230000003068 static effect Effects 0.000 description 5
- BAPJBEWLBFYGME-UHFFFAOYSA-N Methyl acrylate Chemical compound COC(=O)C=C BAPJBEWLBFYGME-UHFFFAOYSA-N 0.000 description 4
- 239000011230 binding agent Substances 0.000 description 4
- 230000000052 comparative effect Effects 0.000 description 4
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- IPCSVZSSVZVIGE-UHFFFAOYSA-N hexadecanoic acid Chemical compound CCCCCCCCCCCCCCCC(O)=O IPCSVZSSVZVIGE-UHFFFAOYSA-N 0.000 description 4
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- 239000006082 mold release agent Substances 0.000 description 4
- 239000000049 pigment Substances 0.000 description 4
- 150000003839 salts Chemical class 0.000 description 4
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 3
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical class [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 3
- 239000004734 Polyphenylene sulfide Substances 0.000 description 3
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 3
- 239000002253 acid Substances 0.000 description 3
- 150000001298 alcohols Chemical class 0.000 description 3
- 239000006229 carbon black Substances 0.000 description 3
- 239000010941 cobalt Substances 0.000 description 3
- 229910017052 cobalt Inorganic materials 0.000 description 3
- GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt atom Chemical class [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 description 3
- 229910052802 copper Inorganic materials 0.000 description 3
- 239000010949 copper Chemical class 0.000 description 3
- 238000010586 diagram Methods 0.000 description 3
- SUPCQIBBMFXVTL-UHFFFAOYSA-N ethyl 2-methylprop-2-enoate Chemical compound CCOC(=O)C(C)=C SUPCQIBBMFXVTL-UHFFFAOYSA-N 0.000 description 3
- 229910052742 iron Inorganic materials 0.000 description 3
- 229910052759 nickel Inorganic materials 0.000 description 3
- 229920006122 polyamide resin Polymers 0.000 description 3
- 239000009719 polyimide resin Substances 0.000 description 3
- 229920000069 polyphenylene sulfide Polymers 0.000 description 3
- 229920001296 polysiloxane Polymers 0.000 description 3
- 229920002379 silicone rubber Polymers 0.000 description 3
- 239000004945 silicone rubber Substances 0.000 description 3
- WRIDQFICGBMAFQ-UHFFFAOYSA-N (E)-8-Octadecenoic acid Natural products CCCCCCCCCC=CCCCCCCC(O)=O WRIDQFICGBMAFQ-UHFFFAOYSA-N 0.000 description 2
- VXNZUUAINFGPBY-UHFFFAOYSA-N 1-Butene Chemical compound CCC=C VXNZUUAINFGPBY-UHFFFAOYSA-N 0.000 description 2
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 2
- OEPOKWHJYJXUGD-UHFFFAOYSA-N 2-(3-phenylmethoxyphenyl)-1,3-thiazole-4-carbaldehyde Chemical compound O=CC1=CSC(C=2C=C(OCC=3C=CC=CC=3)C=CC=2)=N1 OEPOKWHJYJXUGD-UHFFFAOYSA-N 0.000 description 2
- LQJBNNIYVWPHFW-UHFFFAOYSA-N 20:1omega9c fatty acid Natural products CCCCCCCCCCC=CCCCCCCCC(O)=O LQJBNNIYVWPHFW-UHFFFAOYSA-N 0.000 description 2
- JLBJTVDPSNHSKJ-UHFFFAOYSA-N 4-Methylstyrene Chemical compound CC1=CC=C(C=C)C=C1 JLBJTVDPSNHSKJ-UHFFFAOYSA-N 0.000 description 2
- QSBYPNXLFMSGKH-UHFFFAOYSA-N 9-Heptadecensaeure Natural products CCCCCCCC=CCCCCCCCC(O)=O QSBYPNXLFMSGKH-UHFFFAOYSA-N 0.000 description 2
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical class [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 2
- 239000004215 Carbon black (E152) Substances 0.000 description 2
- 229920000089 Cyclic olefin copolymer Polymers 0.000 description 2
- UQSXHKLRYXJYBZ-UHFFFAOYSA-N Iron oxide Chemical compound [Fe]=O UQSXHKLRYXJYBZ-UHFFFAOYSA-N 0.000 description 2
- 239000005639 Lauric acid Substances 0.000 description 2
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 2
- CERQOIWHTDAKMF-UHFFFAOYSA-M Methacrylate Chemical compound CC(=C)C([O-])=O CERQOIWHTDAKMF-UHFFFAOYSA-M 0.000 description 2
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 description 2
- VVQNEPGJFQJSBK-UHFFFAOYSA-N Methyl methacrylate Chemical compound COC(=O)C(C)=C VVQNEPGJFQJSBK-UHFFFAOYSA-N 0.000 description 2
- 239000005642 Oleic acid Substances 0.000 description 2
- ZQPPMHVWECSIRJ-UHFFFAOYSA-N Oleic acid Natural products CCCCCCCCC=CCCCCCCCC(O)=O ZQPPMHVWECSIRJ-UHFFFAOYSA-N 0.000 description 2
- 235000021314 Palmitic acid Nutrition 0.000 description 2
- 239000004642 Polyimide Substances 0.000 description 2
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
- 235000021355 Stearic acid Nutrition 0.000 description 2
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 2
- QYKIQEUNHZKYBP-UHFFFAOYSA-N Vinyl ether Chemical class C=COC=C QYKIQEUNHZKYBP-UHFFFAOYSA-N 0.000 description 2
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 2
- 239000000654 additive Substances 0.000 description 2
- 229910052782 aluminium Inorganic materials 0.000 description 2
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical class [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 2
- 229910052793 cadmium Inorganic materials 0.000 description 2
- BDOSMKKIYDKNTQ-UHFFFAOYSA-N cadmium atom Chemical class [Cd] BDOSMKKIYDKNTQ-UHFFFAOYSA-N 0.000 description 2
- 229910052791 calcium Inorganic materials 0.000 description 2
- 239000011575 calcium Chemical class 0.000 description 2
- NOPFSRXAKWQILS-UHFFFAOYSA-N docosan-1-ol Chemical compound CCCCCCCCCCCCCCCCCCCCCCO NOPFSRXAKWQILS-UHFFFAOYSA-N 0.000 description 2
- UKMSUNONTOPOIO-UHFFFAOYSA-N docosanoic acid Chemical compound CCCCCCCCCCCCCCCCCCCCCC(O)=O UKMSUNONTOPOIO-UHFFFAOYSA-N 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 229920001971 elastomer Polymers 0.000 description 2
- 230000005684 electric field Effects 0.000 description 2
- 239000003822 epoxy resin Substances 0.000 description 2
- 150000002148 esters Chemical class 0.000 description 2
- FJKIXWOMBXYWOQ-UHFFFAOYSA-N ethenoxyethane Chemical compound CCOC=C FJKIXWOMBXYWOQ-UHFFFAOYSA-N 0.000 description 2
- 239000003302 ferromagnetic material Substances 0.000 description 2
- 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 2
- BXWNKGSJHAJOGX-UHFFFAOYSA-N hexadecan-1-ol Chemical compound CCCCCCCCCCCCCCCCO BXWNKGSJHAJOGX-UHFFFAOYSA-N 0.000 description 2
- 229930195733 hydrocarbon Natural products 0.000 description 2
- 150000002430 hydrocarbons Chemical class 0.000 description 2
- QXJSBBXBKPUZAA-UHFFFAOYSA-N isooleic acid Natural products CCCCCCCC=CCCCCCCCCC(O)=O QXJSBBXBKPUZAA-UHFFFAOYSA-N 0.000 description 2
- 238000004898 kneading Methods 0.000 description 2
- 239000011133 lead Substances 0.000 description 2
- SFIHQZFZMWZOJV-HZJYTTRNSA-N linoleamide Chemical compound CCCCC\C=C/C\C=C/CCCCCCCC(N)=O SFIHQZFZMWZOJV-HZJYTTRNSA-N 0.000 description 2
- 239000000314 lubricant Substances 0.000 description 2
- 229910052749 magnesium Inorganic materials 0.000 description 2
- 239000011777 magnesium Substances 0.000 description 2
- 150000002739 metals Chemical class 0.000 description 2
- 125000005395 methacrylic acid group Chemical group 0.000 description 2
- WQEPLUUGTLDZJY-UHFFFAOYSA-N n-Pentadecanoic acid Natural products CCCCCCCCCCCCCCC(O)=O WQEPLUUGTLDZJY-UHFFFAOYSA-N 0.000 description 2
- GLDOVTGHNKAZLK-UHFFFAOYSA-N octadecan-1-ol Chemical compound CCCCCCCCCCCCCCCCCCO GLDOVTGHNKAZLK-UHFFFAOYSA-N 0.000 description 2
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 2
- OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 description 2
- HMZGPNHSPWNGEP-UHFFFAOYSA-N octadecyl 2-methylprop-2-enoate Chemical compound CCCCCCCCCCCCCCCCCCOC(=O)C(C)=C HMZGPNHSPWNGEP-UHFFFAOYSA-N 0.000 description 2
- WWZKQHOCKIZLMA-UHFFFAOYSA-N octanoic acid Chemical compound CCCCCCCC(O)=O WWZKQHOCKIZLMA-UHFFFAOYSA-N 0.000 description 2
- ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid Chemical compound CCCCCCCC\C=C/CCCCCCCC(O)=O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 description 2
- 229960002969 oleic acid Drugs 0.000 description 2
- 229920000647 polyepoxide Polymers 0.000 description 2
- 238000006116 polymerization reaction Methods 0.000 description 2
- 239000000843 powder Substances 0.000 description 2
- WBHHMMIMDMUBKC-XLNAKTSKSA-N ricinelaidic acid Chemical compound CCCCCC[C@@H](O)C\C=C\CCCCCCCC(O)=O WBHHMMIMDMUBKC-XLNAKTSKSA-N 0.000 description 2
- 229960003656 ricinoleic acid Drugs 0.000 description 2
- FEUQNCSVHBHROZ-UHFFFAOYSA-N ricinoleic acid Natural products CCCCCCC(O[Si](C)(C)C)CC=CCCCCCCCC(=O)OC FEUQNCSVHBHROZ-UHFFFAOYSA-N 0.000 description 2
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- 238000012360 testing method Methods 0.000 description 2
- HLZKNKRTKFSKGZ-UHFFFAOYSA-N tetradecan-1-ol Chemical compound CCCCCCCCCCCCCCO HLZKNKRTKFSKGZ-UHFFFAOYSA-N 0.000 description 2
- TUNFSRHWOTWDNC-HKGQFRNVSA-N tetradecanoic acid Chemical compound CCCCCCCCCCCCC[14C](O)=O TUNFSRHWOTWDNC-HKGQFRNVSA-N 0.000 description 2
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- WTARULDDTDQWMU-RKDXNWHRSA-N (+)-β-pinene Chemical compound C1[C@H]2C(C)(C)[C@@H]1CCC2=C WTARULDDTDQWMU-RKDXNWHRSA-N 0.000 description 1
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- BJQFWAQRPATHTR-UHFFFAOYSA-N 1,2-dichloro-4-ethenylbenzene Chemical compound ClC1=CC=C(C=C)C=C1Cl BJQFWAQRPATHTR-UHFFFAOYSA-N 0.000 description 1
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- OEVVKKAVYQFQNV-UHFFFAOYSA-N 1-ethenyl-2,4-dimethylbenzene Chemical compound CC1=CC=C(C=C)C(C)=C1 OEVVKKAVYQFQNV-UHFFFAOYSA-N 0.000 description 1
- JZHGRUMIRATHIU-UHFFFAOYSA-N 1-ethenyl-3-methylbenzene Chemical compound CC1=CC=CC(C=C)=C1 JZHGRUMIRATHIU-UHFFFAOYSA-N 0.000 description 1
- WHFHDVDXYKOSKI-UHFFFAOYSA-N 1-ethenyl-4-ethylbenzene Chemical compound CCC1=CC=C(C=C)C=C1 WHFHDVDXYKOSKI-UHFFFAOYSA-N 0.000 description 1
- CTXUTPWZJZHRJC-UHFFFAOYSA-N 1-ethenylpyrrole Chemical compound C=CN1C=CC=C1 CTXUTPWZJZHRJC-UHFFFAOYSA-N 0.000 description 1
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- IGGDKDTUCAWDAN-UHFFFAOYSA-N 1-vinylnaphthalene Chemical class C1=CC=C2C(C=C)=CC=CC2=C1 IGGDKDTUCAWDAN-UHFFFAOYSA-N 0.000 description 1
- GOXQRTZXKQZDDN-UHFFFAOYSA-N 2-Ethylhexyl acrylate Chemical compound CCCCC(CC)COC(=O)C=C GOXQRTZXKQZDDN-UHFFFAOYSA-N 0.000 description 1
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- RUMACXVDVNRZJZ-UHFFFAOYSA-N 2-methylpropyl 2-methylprop-2-enoate Chemical compound CC(C)COC(=O)C(C)=C RUMACXVDVNRZJZ-UHFFFAOYSA-N 0.000 description 1
- CFVWNXQPGQOHRJ-UHFFFAOYSA-N 2-methylpropyl prop-2-enoate Chemical compound CC(C)COC(=O)C=C CFVWNXQPGQOHRJ-UHFFFAOYSA-N 0.000 description 1
- YHQXBTXEYZIYOV-UHFFFAOYSA-N 3-methylbut-1-ene Chemical compound CC(C)C=C YHQXBTXEYZIYOV-UHFFFAOYSA-N 0.000 description 1
- FEIQOMCWGDNMHM-UHFFFAOYSA-N 5-phenylpenta-2,4-dienoic acid Chemical compound OC(=O)C=CC=CC1=CC=CC=C1 FEIQOMCWGDNMHM-UHFFFAOYSA-N 0.000 description 1
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- 239000005635 Caprylic acid (CAS 124-07-2) Substances 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
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- OYHQOLUKZRVURQ-HZJYTTRNSA-N Linoleic acid Chemical compound CCCCC\C=C/C\C=C/CCCCCCCC(O)=O OYHQOLUKZRVURQ-HZJYTTRNSA-N 0.000 description 1
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- 239000002033 PVDF binder Substances 0.000 description 1
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- 101100101028 Pseudomonas aeruginosa (strain ATCC 15692 / DSM 22644 / CIP 104116 / JCM 14847 / LMG 12228 / 1C / PRS 101 / PAO1) tse3 gene Proteins 0.000 description 1
- WTARULDDTDQWMU-UHFFFAOYSA-N Pseudopinene Natural products C1C2C(C)(C)C1CCC2=C WTARULDDTDQWMU-UHFFFAOYSA-N 0.000 description 1
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- 229920007962 Styrene Methyl Methacrylate Polymers 0.000 description 1
- ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 description 1
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 description 1
- BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 description 1
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- 230000000996 additive effect Effects 0.000 description 1
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- 125000000217 alkyl group Chemical group 0.000 description 1
- 239000000956 alloy Substances 0.000 description 1
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- XCPQUQHBVVXMRQ-UHFFFAOYSA-N alpha-Fenchene Natural products C1CC2C(=C)CC1C2(C)C XCPQUQHBVVXMRQ-UHFFFAOYSA-N 0.000 description 1
- 229910052787 antimony Inorganic materials 0.000 description 1
- WATWJIUSRGPENY-UHFFFAOYSA-N antimony atom Chemical compound [Sb] WATWJIUSRGPENY-UHFFFAOYSA-N 0.000 description 1
- 150000004982 aromatic amines Chemical class 0.000 description 1
- CXOWYMLTGOFURZ-UHFFFAOYSA-N azanylidynechromium Chemical compound [Cr]#N CXOWYMLTGOFURZ-UHFFFAOYSA-N 0.000 description 1
- SKKMWRVAJNPLFY-UHFFFAOYSA-N azanylidynevanadium Chemical compound [V]#N SKKMWRVAJNPLFY-UHFFFAOYSA-N 0.000 description 1
- IRERQBUNZFJFGC-UHFFFAOYSA-L azure blue Chemical compound [Na+].[Na+].[Na+].[Na+].[Na+].[Na+].[Na+].[Na+].[Al+3].[Al+3].[Al+3].[Al+3].[Al+3].[Al+3].[S-]S[S-].[O-][Si]([O-])([O-])[O-].[O-][Si]([O-])([O-])[O-].[O-][Si]([O-])([O-])[O-].[O-][Si]([O-])([O-])[O-].[O-][Si]([O-])([O-])[O-].[O-][Si]([O-])([O-])[O-] IRERQBUNZFJFGC-UHFFFAOYSA-L 0.000 description 1
- 229910052788 barium Chemical class 0.000 description 1
- DSAJWYNOEDNPEQ-UHFFFAOYSA-N barium atom Chemical class [Ba] DSAJWYNOEDNPEQ-UHFFFAOYSA-N 0.000 description 1
- 235000013527 bean curd Nutrition 0.000 description 1
- 229940116226 behenic acid Drugs 0.000 description 1
- 229910052790 beryllium Inorganic materials 0.000 description 1
- ATBAMAFKBVZNFJ-UHFFFAOYSA-N beryllium atom Chemical compound [Be] ATBAMAFKBVZNFJ-UHFFFAOYSA-N 0.000 description 1
- 229930006722 beta-pinene Natural products 0.000 description 1
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Landscapes
- Fixing For Electrophotography (AREA)
- Dry Development In Electrophotography (AREA)
- Electrostatic Charge, Transfer And Separation In Electrography (AREA)
Abstract
Description
【発明の詳細な説明】
[産業上の利用分野]
本発明は、電子写真、静電記録等の後方画像形成方法に
関する。更に詳しく言えば、本発明は中間転写体を用い
て転写を2工程実施して高品位の画像を得る複写方法に
関する。DETAILED DESCRIPTION OF THE INVENTION [Industrial Field of Application] The present invention relates to a method for forming a backward image such as electrophotography or electrostatic recording. More specifically, the present invention relates to a copying method that uses an intermediate transfer member to perform two transfer steps to obtain high-quality images.
[従来の技術]
電子写真方法においては、導電性基板上に形成された光
導電層を一様に帯電し、次いで露光操作により画像状に
除電して静電潜像を形成する。[Prior Art] In an electrophotographic method, a photoconductive layer formed on a conductive substrate is uniformly charged, and then the charge is removed imagewise by an exposure operation to form an electrostatic latent image.
この潜像はトナーと呼ばれる着色樹脂によって可視化さ
れる。この可視化された現像像は紙等の転写紙に静電的
な吸引力により転移せられ、次いで定着ロールを経て転
写紙上に溶融固着され永久画像が得られる。This latent image is made visible with a colored resin called toner. This visualized developed image is transferred to a transfer paper such as paper by electrostatic attraction, and then melted and fixed onto the transfer paper via a fixing roll to obtain a permanent image.
転写工程では、コロトロンあるいはバイアスが印加され
たロールが一般的に用いられている。In the transfer process, a corotron or a roll to which a bias is applied is generally used.
このような復写法では、最終定着画像の品質の低下は多
くの場合、転写工程時における像の乱れに起因すること
が知られている。In such reproduction methods, it is known that the quality of the final fixed image is often degraded due to image disturbance during the transfer process.
この点に鑑み、静電的な転写工程を省略した複写方法も
12案されている。In view of this point, 12 copying methods that omit the electrostatic transfer step have been proposed.
例えば、特公昭37−11646号には感光体上に形成
されたトナー像を転写紙に直接重ね合わせて加熱ロール
等で転写定着する方法が開示されている。For example, Japanese Patent Publication No. 37-11646 discloses a method in which a toner image formed on a photoreceptor is directly superimposed on a transfer paper and then transferred and fixed using a heating roll or the like.
また特公昭46−41679号にはシリコンラバー等に
より形成された中間転写媒体を利用し、一旦感光体上に
形成されたトナー像を非静電的に中間転写媒体に転移(
一種の粘着転写)させ、次いで中間転写媒体と加熱ロー
ルを転写紙を介して接触させ、転写紙に中間転写媒体上
のトナー像を転移させると同時に定着させる複写方法が
開示されている。Furthermore, in Japanese Patent Publication No. 46-41679, an intermediate transfer medium made of silicone rubber or the like is used to non-electrostatically transfer a toner image formed on a photoreceptor to the intermediate transfer medium.
A copying method is disclosed in which a toner image on the intermediate transfer medium is simultaneously transferred and fixed to the transfer paper by bringing an intermediate transfer medium into contact with a heating roll via a transfer paper.
更に、特公昭48−22763号には導電性磁性トナー
とシリコンラバーの中間転写媒体を組合わせた熱転写定
着法が開示されている。Furthermore, Japanese Patent Publication No. 48-22763 discloses a thermal transfer fixing method that combines a conductive magnetic toner and a silicone rubber intermediate transfer medium.
更に、特開昭56−138742号では耐熱性樹脂から
なる電荷保持層とシリコンラバー等の中間転写媒体を用
いた熱転写定着法が開示されている。Further, JP-A-56-138742 discloses a thermal transfer fixing method using a charge retention layer made of a heat-resistant resin and an intermediate transfer medium such as silicone rubber.
これらの複写方法は、プロセスの簡易化を自差してスタ
ートしたものであるが、次第に複写画像の品質の向上、
すなわち従来のコロトロン等による静電気力を利用した
複写方法において転写紙上でトナー像の乱れが発生し、
最終定着画像においてライン像周辺の乱れ、解像度の低
下、ソリッド像の粒状性の低下を招く欠点を回避するた
めの手段として注目されてきたものである。These copying methods started with the aim of simplifying the process, but gradually improved the quality of copied images and
In other words, in conventional copying methods that utilize electrostatic force using corotrons, etc., disturbances occur in the toner image on the transfer paper.
This method has been attracting attention as a means for avoiding defects that cause disturbances around line images, reduction in resolution, and reduction in graininess of solid images in the final fixed image.
[発明が解決しようとする問題点]
従来技術では、単に転写工程のみを非静電的な手段とす
ることによって複写画像の品質を高めようとしているが
、本発明の目的は画像形成システム全体、覆なわち潜像
形成、現像、転写、定着という一連のプロセスを通して
、高品質な画像、特に100〜200線/インチの網点
画像をその階調性を損うことなく原稿に忠実に再坦でき
る複写方法を提供することにある。[Problems to be Solved by the Invention] In the prior art, an attempt has been made to improve the quality of copied images by simply using non-electrostatic means for the transfer process. Through a series of processes including latent image formation, development, transfer, and fixing, high-quality images, especially halftone images of 100 to 200 lines/inch, can be reproduced faithfully to the original without losing gradation. The objective is to provide a copying method that is possible.
[問題点を解決するための手段]
本発明は表面が平滑な記録媒体上に原稿に忠実な静電潜
像を形成する工程、前記の静電潜像を導電性トナーによ
り均一薄層状態で現像する工程、得られたトナー像を表
面が平滑な中間転写媒体に非静電的に転写する工程、中
間転写媒体上のトナー像を記録シートを介在させて加熱
ロールにて押圧し記録シートに転写定着する工程からな
る複写方法を提供したものである。[Means for Solving the Problems] The present invention involves a step of forming an electrostatic latent image faithful to an original on a recording medium with a smooth surface, and forming the electrostatic latent image into a uniform thin layer using conductive toner. A step of developing, a step of non-electrostatically transferring the obtained toner image to an intermediate transfer medium with a smooth surface, and a step of pressing the toner image on the intermediate transfer medium with a heating roll with a recording sheet interposed therebetween to form a recording sheet. The present invention provides a copying method comprising a step of transferring and fixing.
第1図に示すように本発明の複写方法では、例えば感光
体ベルト1にまずコロトロンにて均一帯電を施しく第1
図(a))、次いで画像露光して静電潜像を形成しく第
1図(b))、この静電潜像を高抵抗トナーにより現像
しく第1図(C))、得られたトナー像を一旦中間転写
媒体2に非静電的に押圧ロール13にて一次転写しく第
1図(d))、次いで一次転写像を記録シート3に加熱
ロール15を用いて二次転写定着して永久画像が形成さ
れる(第1図(e))。As shown in FIG. 1, in the copying method of the present invention, for example, a photoreceptor belt 1 is first uniformly charged with a corotron, and a first
(a)), then imagewise exposure is performed to form an electrostatic latent image (FIG. 1(b)), and this electrostatic latent image is developed with a high resistance toner (FIG. 1(C)), and the resulting toner is The image is first transferred to the intermediate transfer medium 2 non-electrostatically using the pressure roll 13 (FIG. 1(d)), and then the primary transfer image is secondarily transferred and fixed onto the recording sheet 3 using the heating roll 15. A permanent image is formed (FIG. 1(e)).
以下第2図に示す本発明の方法を実施する複写システム
例を参照しながら本発明の詳細な説明する。The present invention will now be described in detail with reference to an example of a copying system implementing the method of the present invention shown in FIG.
(1)潜像の形成工程
感光体を均一帯電した後に画像露光して静電潜像を形成
する。第2図のシステムでは、a方向に移動するベルト
状感光体1を帯電器4により帯電した後露光5によって
潜像が形成される。(1) Step of forming a latent image After the photoreceptor is uniformly charged, it is imagewise exposed to form an electrostatic latent image. In the system shown in FIG. 2, a latent image is formed by exposure 5 after the belt-shaped photoreceptor 1 moving in the direction a is charged by a charger 4.
感光体は必ずしもベルト状でなくてもよく、ドラム状の
ものも使用可能である。The photoreceptor does not necessarily have to be belt-shaped; a drum-shaped one can also be used.
感光体の材料としては、無機系の非晶質材料としてSe
、Se/As、As2 Se3 、Se/Te、Si、
S、結晶性材料としてCdS、CdSe、7nO,Ti
O2、有機系のビスアゾ顔料、フタロシアニン顔料、ス
クェアリウム顔料等の電荷発生材料と芳香族アミン、ヒ
ドラゾン等の電荷輸送材料とからなるものが使用可能で
ある。As the material for the photoreceptor, Se is used as an inorganic amorphous material.
, Se/As, As2 Se3 , Se/Te, Si,
S, CdS, CdSe, 7nO, Ti as crystalline materials
A material comprising a charge generating material such as O2, an organic bisazo pigment, a phthalocyanine pigment, or a squareium pigment, and a charge transporting material such as an aromatic amine or hydrazone can be used.
高品質な複写画像を得るための感光体への要求特性とし
テハ、表面形状、PI D C(Photo In−d
uced Decay Curve >特性、表面抵抗
が挙げられる。The characteristics required for a photoconductor to obtain high-quality copied images are photoreceptor, surface shape, PIDC
uced Decay Curve >Characteristics, surface resistance.
表面形状に関しては、例えばZnOの如き分散型の感光
体では、その表面粗さが深さ0.5μ以上の凹凸の周波
数5cycle/mm、深さ7μと粗く、感光体上にト
ナー像を形成した場合、その凹部にトナー粒子が入り込
み中間転写媒体への一次転写において、感光体の凹部に
埋まり込んだトナー粒子は中間転写媒体に転移される画
像の白恢けを発生させるばかりでなく、感光体のクリー
ニングにおいても負荷を生ずる。Regarding the surface shape, for example, in a dispersion-type photoreceptor such as ZnO, the surface roughness is rough with a frequency of 5 cycles/mm and a depth of 7μ with unevenness of 0.5μ or more, and a toner image is formed on the photoreceptor. In this case, toner particles enter the recesses, and during the primary transfer to the intermediate transfer medium, the toner particles embedded in the recesses of the photoreceptor not only cause blurring of the image transferred to the intermediate transfer medium, but also cause the image to be transferred to the intermediate transfer medium. Cleaning also creates a load.
3e系のような蒸着型の感光体では、非常に良好な一次
転写特性が1りられるが、ZnOのような分散型の感光
体でもその表面を平滑処理することにより良好な一次転
写特性を1qることかできる。Vapor-deposited photoreceptors such as 3e type photoreceptors have very good primary transfer characteristics, but even dispersion type photoreceptors such as ZnO can have good primary transfer characteristics by smoothing the surface. I can do that.
実験的には表面粗さが深さ0,5μ以上の凹凸の周波数
1 cycle/m以下、深さ1μ以下の場合にほぼ1
00%の一次転写が達成できることが確認された。Experimentally, the frequency of irregularities with a surface roughness of 0.5μ or more in depth is 1 cycle/m or less, and when the depth is 1μ or less, the frequency is approximately 1.
It was confirmed that 0.00% primary transfer could be achieved.
PIDC特性に関しては、特に網点再現には急峻な、す
なわち2値的特性のものが好ましい。Regarding the PIDC characteristic, a steep one, that is, a binary characteristic is preferable, especially for halftone dot reproduction.
PIDC特性(センシメトリー〉は感光体への露光量、
帯電電位等の制御により調節が可能である。PIDC characteristics (sensimetry) is the amount of exposure to the photoreceptor,
Adjustment is possible by controlling the charging potential, etc.
表面抵抗に関しては、特に現像剤との絡みで潜像電荷の
リークを抑えるため、光導電層上に誘電フィルムあるい
はスプレー塗布による絶縁性皮膜を形成することが好ま
しい。また皮膜中に導電性金属微粉を混入し、その抵抗
を制011vることも可能である。Regarding the surface resistance, it is preferable to form a dielectric film or an insulating film by spray coating on the photoconductive layer, particularly in order to suppress leakage of latent image charges due to entanglement with the developer. It is also possible to mix conductive metal fine powder into the film to control its resistance.
また耐熱性という観点からはa−3iが好ましく、同様
に無機系光導電性材料、例えばCdS、Cd53e、
Cd3e、Zn5e、ZnCd5、TiO2、Zn0X
CdS−CdCO3を耐熱性樹脂中に分散させたものが
適用できる。耐熱性樹脂としてはフッ素系樹脂、ポリイ
ミド樹脂、ポリアミド樹脂、ポリイミドアミド樹脂、ポ
リアリールスルホン樹脂、ポリフェニレンサルファイド
樹脂、熱硬化性アクリル樹脂、熱硬化性アルキッド樹脂
、エポキシ樹脂、およびこれらの混合物等、この分野で
耐熱性樹脂として広く用いられるものが用いられる。In addition, from the viewpoint of heat resistance, a-3i is preferable, and similarly inorganic photoconductive materials such as CdS, Cd53e,
Cd3e, Zn5e, ZnCd5, TiO2, Zn0X
CdS-CdCO3 dispersed in a heat-resistant resin can be used. Heat-resistant resins include fluorine resins, polyimide resins, polyamide resins, polyimide amide resins, polyarylsulfone resins, polyphenylene sulfide resins, thermosetting acrylic resins, thermosetting alkyd resins, epoxy resins, and mixtures thereof. A material widely used as a heat-resistant resin in the field is used.
これらの耐熱性樹脂の具体例としで、含フツ素樹脂とし
てはポリー四フッ化エチレン、四フフ化エチレンー六−
フツ化プロピレン共重合体、ポリ−(三フッ化塩化エチ
レン)、ポリ−フッ化ビニリデン、三フッ化塩化エチレ
ンーフッ化ビニリデン共重合体、ポリ−パーフルオロア
ルキレン(PP八〉、ボリーヒ′ニルヘプタフルオロブ
チレートアミジン(ナイロン6)、ザイデル(ナイロン
66)、カプトン(ポリイミド樹脂)、ライドンpps
v−iタイプ[ポリフェニレンサルファイド樹脂、採土
ガ谷化学U製]、アストレルー560[ボリアリールス
ルホン樹脂、3M社製コが挙げられる。前記した耐熱性
樹脂の中でもフッ素系樹脂、ポリイミド樹脂、ポリアミ
ド樹脂、ポリイミドアミド樹脂またはポリフェニレンサ
ルファイド樹脂、あるいはこれらの混合物が好ましい。Specific examples of these heat-resistant resins include polytetrafluoroethylene, tetrafluoroethylene-6-
Propylene fluoride copolymer, poly(ethylene chloride trifluoride), polyvinylidene fluoride, ethylene chloride trifluoride-vinylidene fluoride copolymer, poly-perfluoroalkylene (PP8), polyhinylheptafluorobutylene Rateamidine (nylon 6), Seidel (nylon 66), Kapton (polyimide resin), Rydon pps
Examples include v-i type [polyphenylene sulfide resin, manufactured by Idogatani Kagaku U] and Astrelu 560 [boaryaryl sulfone resin, manufactured by 3M Company]. Among the heat-resistant resins mentioned above, fluororesins, polyimide resins, polyamide resins, polyimide amide resins, polyphenylene sulfide resins, or mixtures thereof are preferred.
潜像の形成工程においては、透過原稿を用いた密着透過
露光が好ましいが、原稿作成の繁雑さ、密着精度を増す
だめの吸引等の装置が必要となり装置の複雑化、大型化
から制約を受ける。実用的には、トラッキングエラー、
ベロシティ−エラー等を抑えるためにベルト状の感光体
を使用し、平面を利用した静止露光あるいは原稿との相
対位置が変わらないとみなせる状態での露光が好ましい
。In the process of forming a latent image, contact transmission exposure using a transparent original is preferable, but it is restricted by the complexity of creating the original, the need for suction equipment to increase contact accuracy, and the complexity and size of the equipment. . In practical terms, tracking error,
In order to suppress velocity errors and the like, it is preferable to use a belt-shaped photoreceptor and perform static exposure using a flat surface or exposure in a state where the relative position with respect to the original can be considered unchanged.
高速化を考慮した場合、ベルト状感光体でのフラッシュ
露光が特に適している。When considering high speed, flash exposure using a belt-shaped photoreceptor is particularly suitable.
(2)現像工程
原稿に忠実な潜像を形成した後は現像Ia6によりトナ
ー現像が行われる。(2) Developing process After forming a faithful latent image on the original, toner development is performed by the developer Ia6.
この現像工程では一次工程である転写での像の拡がり、
潰れを考慮し、薄層均一現像を行うことが必須である。In this development process, the image spreads in the primary process of transfer,
It is essential to take uniform development into a thin layer in consideration of crushing.
特にトナーの粒径よりもトナー像の高さくパイルハイド
)が重要でおり、実験的には10〜20μの範囲がライ
ン像の拡がり、網点画像の場合はハイライトからシャド
ー域にわたるドツトの拡がり、潰れを抑える事が可能で
あることをつきとめた。In particular, the height of the toner image (pile hide) is more important than the toner particle size, and experimentally the range of 10 to 20μ is the spread of line images, and in the case of halftone images, the spread of dots from highlights to shadows. We found that it is possible to suppress the collapse.
上記均一薄層現像の具体的方法としては、導電性−成分
トナーが良好な結果をもたらり。As a specific method for developing the uniform thin layer, conductive component toners yield good results.
トナーの電気抵抗値としては、実験的に103v /
cmの電場で103〜1011Ω” cmのものか好ま
しいことが確認された。The electrical resistance value of toner is experimentally 103v/
It was confirmed that 10 3 to 10 11 Ω” cm is preferable in an electric field of cm.
また磁性、非磁性トナーを問わず使用づることができる
が、搬送供給の簡便さからは磁性トナーか、カラー化の
観点からは非磁性トナーか好ましい。Although either magnetic or non-magnetic toner can be used, magnetic toner is preferred from the viewpoint of ease of transport and supply, and non-magnetic toner is preferred from the viewpoint of coloring.
磁性トナーの場合は磁気ブラシ現像法あるいは磁気テー
プ等を用いて磁性トナーをテープ上に薄層に塗イl、、
タッヂダウンあるいはジャンピングを行なう現像法か適
用できる。In the case of magnetic toner, use a magnetic brush development method or magnetic tape to apply a thin layer of magnetic toner onto the tape.
A developing method that performs step-down or jumping can be applied.
非磁性トナーの場合は、10〜1014Ω・cm稈度の
ドナーロールに対し、金属の薄板を押しつけ、トナーの
薄層を形成する方式、あるいはインプレッション方式等
が適用できる。In the case of non-magnetic toner, a method in which a thin metal plate is pressed against a donor roll having a culm of 10 to 1014 Ω·cm to form a thin layer of toner, or an impression method can be applied.
トナーとしては粒度(平均粒径)が10μ以下、好まし
くは1〜5μのものかよいことが実験的に確認された。It has been experimentally confirmed that the toner has a particle size (average particle size) of 10 microns or less, preferably 1 to 5 microns.
印刷用インク、液体現像剤の粒子ナイスを考慮すれば画
質の向−ヒ(特に低濃度ソリッド像の粒状性、解像性の
向上、網点画像のドツトの形状、DmilXの向上)に
は細かいものほど好結果が19られるが、製造面からの
制約およびハンドリング等から限界かある。Considering the particle size of printing ink and liquid developer, it is important to improve image quality (particularly graininess of low-density solid images, improvement of resolution, dot shape of halftone images, and improvement of DmilX). Although very good results have been achieved, there are limits due to manufacturing constraints and handling.
粒度弁イ[は、選択用像、あるいは−次転写、二次転写
での転移〈即ち、押圧力が各トナー粒子に均一に作用す
ることが望ましいこと)を考慮すると狭い方が良く、実
験的に分布の指標dqo/d、。It is better to have a narrower particle size in consideration of the selection image, or the transfer during the next transfer or secondary transfer (that is, it is desirable that the pressing force acts uniformly on each toner particle), and the experimental The distribution index dqo/d.
で2〜4か良好な結果を与えることを見い出した。It was found that 2 to 4 gave good results.
トナー材料としては、−次転写での感光体へのオフセッ
ト防止、二次転写での中間転写媒体へのオフセット防1
の観点からトナー中に離型剤を添加してもよい。The toner material is used to prevent offset to the photoconductor during secondary transfer, and to prevent offset to intermediate transfer medium during secondary transfer.
From this point of view, a release agent may be added to the toner.
この離型剤はトノ゛−用結看樹脂に離型性を付与したも
のであってもよいし、離型剤として添加してもよい。This mold release agent may be one that imparts mold release properties to the toner binding resin, or may be added as a mold release agent.
トナー用結椙樹脂に離型性を付与したものとしては、ス
チレン系中量体の重合体、仙のビニル系単ω体の重合体
、またはスチレン系中量体と他のビニル系単量体との共
重合体が挙げられる。Examples of resins for toners that have releasable properties include polymers of styrene-based intermediates, vinyl mono-omega polymers, or styrene-based intermediates and other vinyl monomers. Examples include copolymers with
スチレン系中量体としては、例えばスチレン、m−メチ
ルスチレン、p−メチルスチレン、p−エチルスチレン
、2,4−ジメチルスチレン、p−tert−ブヂルス
チレン、p−0−へキシルスチレン、p−メ]〜キシス
チレン、p−フェニルスチレン、3,4−ジクロルスチ
レン等のスチレン及びその誘導体が挙げられ、スチレン
単量体が最も好ましい。伯のビニル系単量体としては、
例えばエチレン、プロピレン、ブチレン、イソブチレン
などのエチレン系不飽和モノオレフィン類;塩化ビニル
、塩化ビニリデンなどのハロゲン化ビニル類:酢酸ビニ
ル、ベンジェ酸ビニル、醋酸ビニルなどのビニルエステ
ル類、アクリル酸メチル、アクリル酸エチル、アクリル
酸イソブブル、アクリル酸ドデシル、アクリル酸2−エ
チルヘキシル、アクリル酸2−クロルエチル、アクリル
酸フェニル、α−クロルアクリル酸メチル、メタクリル
酸メチル、メタクリル酸エチル、メタクリル酸イソブヂ
ル、メタクリル酸2−エチルヘキシル、メタアクリル酸
ステアリル、メタアクリル酸フェニル、メタアクリル酸
ジメヂルアミンエチル、メタアクリル酸ジエブルアミノ
エチルなどのα−メチレン脂肪族モノカルボン酸エステ
ル類;アクリロニトリル、アクリルアミドなどのアクリ
ル酸もしくはメタアクリルrti誘導体;ビニルエチル
エーテルなどのビニルエーテル類:ビニルメチルクドン
などのビニルケトン類;N−ビニルピロール、N−ビニ
ルカルバゾールなどのN−ビニル化合物:ビニルナフタ
リン類などを挙げることができる。Examples of styrenic intermediates include styrene, m-methylstyrene, p-methylstyrene, p-ethylstyrene, 2,4-dimethylstyrene, p-tert-butylstyrene, p-0-hexylstyrene, and p-methylstyrene. ] to styrene and its derivatives such as xystyrene, p-phenylstyrene, and 3,4-dichlorostyrene, and styrene monomers are most preferred. As Haku's vinyl monomers,
For example, ethylenically unsaturated monoolefins such as ethylene, propylene, butylene, and isobutylene; vinyl halides such as vinyl chloride and vinylidene chloride; vinyl esters such as vinyl acetate, vinyl benzoate, and vinyl acetate; methyl acrylate, and acrylic Ethyl acid, isobutyl acrylate, dodecyl acrylate, 2-ethylhexyl acrylate, 2-chloroethyl acrylate, phenyl acrylate, methyl α-chloroacrylate, methyl methacrylate, ethyl methacrylate, isobutyl methacrylate, 2-ethyl methacrylate α-methylene aliphatic monocarboxylic acid esters such as ethylhexyl, stearyl methacrylate, phenyl methacrylate, dimethylamine ethyl methacrylate, and diebruaminoethyl methacrylate; acrylic acid or methacrylic acid such as acrylonitrile and acrylamide Examples include rti derivatives; vinyl ethers such as vinyl ethyl ether; vinyl ketones such as vinyl methylbutone; N-vinyl compounds such as N-vinylpyrrole and N-vinylcarbazole; and vinylnaphthalenes.
共重合体の具体例としてはスチレン−酢酸ビニル共重合
体、スチレン−メタクリル酸メチル共重合体、スチレン
−アクリル酸メチル共重合体、スチレン−メタクリル酸
2−エチルヘキシル共重合体、スチレン−アクリル酸2
−クロルエチル共手合体もしくはスチレン−メタクリル
酸フェニル共重合体が挙げられる。そしてこれらの重合
体は重量平均分子量で3,000以上、好ましくは3.
000〜500、000の分子量を有することか好まし
い。Specific examples of copolymers include styrene-vinyl acetate copolymer, styrene-methyl methacrylate copolymer, styrene-methyl acrylate copolymer, styrene-2-ethylhexyl methacrylate copolymer, and styrene-acrylic acid 2 copolymer.
-chloroethyl copolymer or styrene-phenyl methacrylate copolymer. These polymers have a weight average molecular weight of 3,000 or more, preferably 3.
It is preferable to have a molecular weight of 000 to 500,000.
ざらにこれらの重合体は重量平均分子ffi/vl平均
分子串平均分子塩上でおることか好ましい。It is generally preferred that these polymers have a weight average molecular weight ffi/vl average molecular weight average molecular salt.
添加剤としての離型剤としては、例えば低分子量オレフ
ィン重合体、脂肪酸の金属塩、高級脂肪酸、脂肪酸アミ
ド、高級アルコール、炭化水素系滑剤、脂肪酸エステル
が挙げられる。Examples of the mold release agent as an additive include low molecular weight olefin polymers, metal salts of fatty acids, higher fatty acids, fatty acid amides, higher alcohols, hydrocarbon lubricants, and fatty acid esters.
本発明の現像剤において使用される低分子量オレフィン
重合体は、単量体成分としてオレフィンのみを含有する
オレフィン単合体または単量体成分としてオレフィン以
外の単量体を含有するオレフィン共重合体であって、低
分子のものである。The low molecular weight olefin polymer used in the developer of the present invention is an olefin monopolymer containing only an olefin as a monomer component or an olefin copolymer containing a monomer other than olefin as a monomer component. It is a low-molecular substance.
単量体成分としてのオレフィンには、たとえばエチレン
、プロピレン、ブテン−1、オクテン−1もしくは不飽
和結合の位置を異にするそれらの同hX体または、たと
えば3−メチル−1−ブテン、3−プロピル−5−メチ
ル−2−ヘキセン等のそれらに分岐鎖としてアルキル基
を導入されたもの等あらゆるオレフィンが包含される。Olefins as monomer components include, for example, ethylene, propylene, butene-1, octene-1 or their hX forms with different positions of unsaturated bonds, or, for example, 3-methyl-1-butene, 3- All kinds of olefins such as propyl-5-methyl-2-hexene and the like having an alkyl group introduced as a branched chain are included.
また、オレフィンとともに共重合体を形成する単量体成
分としてオレフィン以外の単量体としては、たとえばビ
ニルメチルエーテル、ビニルフェニルエーテル等のビニ
ルエーテル類、たとえば酢酸ビニル等のビニルエステル
類、たとえばテトラクロロエチレン、塩化ビニル、塩化
ビニリデン、テトラクロロエチレン等のハロオレフィン
類、たとえばアクリル酸メチル、アクリル酸エチル、メ
タアクリル酸メチル、メタアクリル酸エチル、メタアク
リル酸ロー1チル、メタアクリル酸ステアリル、メタア
クリルll!N、N−ジメチルアミノエチル、メタアク
リルlt−ブチルアミノエチル等のアクリル酸エステル
類もしくはメタアクリル酸エステル類、たとえばアクリ
[]ニトリル、N、N−ジメチルアクリルアミド等のア
クリル型誘導体、たとえばアクリル酸、メタアクリル酸
等の有機酸類、ジエチルフマレ−1・、β−ピネン等種
々のものをあげることができる。In addition, examples of monomers other than olefins that form copolymers with olefins include vinyl ethers such as vinyl methyl ether and vinyl phenyl ether, vinyl esters such as vinyl acetate, tetrachloroethylene, chloride, etc. Haloolefins such as vinyl, vinylidene chloride, and tetrachloroethylene, such as methyl acrylate, ethyl acrylate, methyl methacrylate, ethyl methacrylate, rho-1-tyl methacrylate, stearyl methacrylate, and methacrylic! Acrylic acid esters or methacrylic acid esters such as N,N-dimethylaminoethyl and methacrylic lt-butylaminoethyl; for example, acryl[]nitrile; acrylic type derivatives such as N,N-dimethylacrylamide; for example, acrylic acid; Various organic acids such as methacrylic acid, diethyl fumare-1., and β-pinene can be mentioned.
低分子量オレフィン重合体は、前記の如きオレフィンを
少なくとも2種以−ヒ単量体成分として含有するオレフ
ィンのみからなるオレフィン重合体、たとえば′エチレ
ンープロピレン共重合体、エヂレンーブテン共重合体、
エチレン−ペンテン共重合体、プロピレン−ブテン共重
合体、プロピレン−ペンテン共重合体、エチレン−3−
メチル−1−ブテン共重合体、エチレン−プロピレン−
ブテン共重合体等または前記の如きオレフィンの少なく
とも1種と前記のごときオレフィン以外の単量体の少な
くとも1種とを単量体成分として含(1するオレフィン
共重合体、たとえばエチレン−ビニルアセテート共重合
体、エチレンーヒニルメチルエーテル共重合体、エチレ
ン−塩化ビニル共重合体、Tチレンーアクリル酸メチル
共重合体、エチレン−メタアクリル酸メチル共重合体、
エチレン−アクリル酸共重合体、プロピレン−M!ビニ
ル共重合体、プロピレン−ビニルエチルエーテル共重合
体、プロピレン−アクリル酸エチル共重合体、プロピレ
ン−メタアクリル酸共重合体、ブテン−メタアクリル酸
メチル共重合体、ペンテン−酢酸ビニル共重合体、ヘキ
セン−酢酸ビニル共重合体、エチレン−プロピレン−酢
酸ビニル共重合体、エチレン酢酸ビニル−ビニルメチル
エーテル共重合体等でおる。Low molecular weight olefin polymers are olefin polymers consisting only of olefins containing at least two of the above-mentioned olefins as monomer components, such as ethylene-propylene copolymers, ethylene-butene copolymers,
Ethylene-pentene copolymer, propylene-butene copolymer, propylene-pentene copolymer, ethylene-3-
Methyl-1-butene copolymer, ethylene-propylene
An olefin copolymer, such as ethylene-vinyl acetate, containing as a monomer component at least one of the above-mentioned olefins and at least one monomer other than the above-mentioned olefins. polymer, ethylene-hinyl methyl ether copolymer, ethylene-vinyl chloride copolymer, T-tyrene-methyl acrylate copolymer, ethylene-methyl methacrylate copolymer,
Ethylene-acrylic acid copolymer, propylene-M! Vinyl copolymer, propylene-vinylethyl ether copolymer, propylene-ethyl acrylate copolymer, propylene-methacrylate copolymer, butene-methyl methacrylate copolymer, pentene-vinyl acetate copolymer, Hexene-vinyl acetate copolymer, ethylene-propylene-vinyl acetate copolymer, ethylene-vinyl acetate-vinyl methyl ether copolymer, etc.
低分子量オレフィン重合体のうち単量体成分としてオレ
フィン以外の単量体を含有するものにおいては、共重合
体中に含有するオレフィン成分はできるだけ多いものが
望ましい。なぜなら一般にオレフィン成分の含有量が小
になるほど離型性か小さくなり、またトナーの流動性、
画像性等の特性が劣化する傾向があるからである。Among low-molecular-weight olefin polymers that contain monomers other than olefins as monomer components, it is desirable that the copolymer contain as many olefin components as possible. This is because, in general, the smaller the content of the olefin component, the lower the releasability, and the lower the fluidity of the toner.
This is because characteristics such as image quality tend to deteriorate.
このため共重合体中のオレフィン成分の含有間はできる
だけ多いものが望ましく、とくに約50モル%以上のオ
レフィン成分を含有するものが有効に使用される。For this reason, it is desirable that the content of the olefin component in the copolymer be as large as possible, and in particular, a copolymer containing about 50 mol% or more of the olefin component is effectively used.
低分子量オレフィン重合体の分子量は通常の高分子化合
物で言う低分子量の概念に含まれるものであればよいが
、一般的には手早平均分子量で1.000〜45,00
0.好ましくは2,000〜6,000のものである。The molecular weight of the low molecular weight olefin polymer may be anything that is included in the concept of low molecular weight in ordinary polymer compounds, but it is generally a quick average molecular weight of 1.000 to 45,00.
0. Preferably it is 2,000 to 6,000.
低分子量オレフィン重合体は軟化点が100〜180’
C,特に130〜160°Cを有するものか好ましい。Low molecular weight olefin polymers have a softening point of 100-180'
C, especially those having a temperature of 130 to 160°C are preferred.
低分子量オレフィン重合体の使用量はトナーの樹脂成分
100重量当り1〜20重量部、好ましくは3〜15重
量部であり、1重量部以下では充分な離型性付与効果を
有しない場合かあり、また20手量部以上ではトナーの
他の性質を低下させる傾向かおることかあるので好まし
くない。The amount of the low molecular weight olefin polymer used is 1 to 20 parts by weight, preferably 3 to 15 parts by weight, per 100 parts by weight of the resin component of the toner, and if it is less than 1 part by weight, it may not have a sufficient effect of imparting release properties. If the amount is more than 20 parts by weight, it may tend to deteriorate other properties of the toner, which is not preferable.
本発明の現像剤に使用される離型剤の他の例としては、
脂肪酸の金属塩として、ラウリン酸、ミリスチン酸、パ
ルミチン酸、ステアリン酸、アラキン酸、ベヘン酸、オ
レイン酸、カプリル酸、力プロン酸、リノール酸、リシ
ノール酸またはりシルイン酸の鉛、亜鉛、マグネシウム
、コバルト、銅、カルシウム、カドミウム、鉄、ニッケ
Jし、アルミニウムまたはバリウムの金属塩か挙げられ
、高級脂肪酸として通常炭素原子数8以上のデカン酸、
ラウリン酸、ミリスチン酸、パルミチン酸、ステアリン
酸、オレイン酸、リノール酸またはリシノール酸か挙げ
られ、脂肪酸アミドとして、ラウリン酸アミド、ミリス
チン酸アミド、パルミチン酸アミド、ステアリン酸アミ
ド、アラキン酸アミド、ベヘン酸アミド、オレイン酸ア
ミド、リノール酸アミド、リノール酸アミド、ガドレン
酸アミド、エルカ酸アミド、セラコレイン酸アミド:ビ
ス脂肪酸アミドとしては、ビスラウリン酸アミド、ヒス
ミリスチン酸アミド、ヒスパルミチン酸アミド、ビスス
テアリン酸アミド、N、N’−シトデカノイル−エチレ
ンジアミンが挙げられ、高級アルコールとして、ラウリ
ルアルコール、ミリスチルアルコール、セチルアルコー
ル、ステアリルアルコール、ベヘニルアルコールまたは
オレイルアルコールが挙げられ、脂肪酸エステルとして
、脂肪酸と一価アルコールとのエステルまたは脂肪酸と
多価アルコールとの全エステルもしくは部分エステルが
挙げられ、そして炭化水素系滑剤として、天然パラフィ
ン、合成パラフィン、マイクロワックス、塩素化パラフ
ィンが挙げられる。Other examples of release agents used in the developer of the present invention include:
Metal salts of fatty acids include lead, zinc, magnesium, lauric acid, myristic acid, palmitic acid, stearic acid, arachic acid, behenic acid, oleic acid, caprylic acid, cyproproic acid, linoleic acid, ricinoleic acid or ricylic acid, Examples include metal salts of cobalt, copper, calcium, cadmium, iron, nickel, aluminum or barium; higher fatty acids include decanoic acid, which usually has 8 or more carbon atoms;
Examples include lauric acid, myristic acid, palmitic acid, stearic acid, oleic acid, linoleic acid or ricinoleic acid; fatty acid amides such as lauric acid amide, myristic acid amide, palmitic acid amide, stearic acid amide, arachidic acid amide, behenic acid Amide, oleic acid amide, linoleic acid amide, linoleic acid amide, gadolenic acid amide, erucic acid amide, ceracoleic acid amide: As bis fatty acid amide, bislauric acid amide, hismyristic acid amide, hispalmitic acid amide, bisstearic acid amide , N,N'-cytodecanoyl-ethylenediamine; higher alcohols include lauryl alcohol, myristyl alcohol, cetyl alcohol, stearyl alcohol, behenyl alcohol, and oleyl alcohol; fatty acid esters include esters of fatty acids and monohydric alcohols; Examples include full or partial esters of fatty acids and polyhydric alcohols, and hydrocarbon lubricants include natural paraffins, synthetic paraffins, microwaxes, and chlorinated paraffins.
これらの離型剤の現像剤に対する添Iノ[1量は現像剤
に対して0.1〜65手量%、好ましくは0.2〜20
重量%である。The amount of these release agents added to the developer is 0.1 to 65% by weight, preferably 0.2 to 20% by weight based on the developer.
Weight%.
現像剤の一般的添加剤および製造方法について述l〈る
。General developer additives and manufacturing methods will be described below.
トナーは前記した離型剤を含有する他、トナー用結着樹
脂をも含有覆る。これらの樹脂は前記した離型性を有す
るものであってもよく、離型性を有しない、例えばエポ
キシ樹脂、ポリエステル樹脂、ポリアミド樹脂であって
もよい。In addition to containing the above-mentioned release agent, the toner also contains a binder resin for toner. These resins may have the above-mentioned mold releasability, or may not have mold releasability, such as epoxy resins, polyester resins, and polyamide resins.
本発明に係るトナーには必要に応じて顔料、染料等の任
意の着色剤を添加することができる。これらの着色剤は
公知のものであって、例えばカーボンブラック、ニグロ
シン染料、アニリンブルー、カルフォイルブル−、クロ
ムイエロー、ウルトラマリンブルー、デュポンオイルレ
ッド、キノリンイエロー、メチレンブルークロリド、フ
タロシアニンブルー、マラカイトグリーンオギザレート
、ランプブラック、オイルブラック、アゾオイルブラッ
ク、ローズペンカル及びそれらの混合物でおる。又、印
書された文書の従来のゼログラフ複写か所望されている
所では、トナーは、例えばカーボンブラックの如き黒色
染料又はアマプラストブラック染料の如き、黒色染料か
ら製造されてしよい。Any coloring agent such as a pigment or dye can be added to the toner according to the present invention, if necessary. These coloring agents are known ones, such as carbon black, nigrosine dye, aniline blue, carfoil blue, chrome yellow, ultramarine blue, DuPont oil red, quinoline yellow, methylene blue chloride, phthalocyanine blue, malachite green ogyza. black, lamp black, oil black, azo oil black, rose pencal and mixtures thereof. Also, where conventional xerographic reproduction of printed documents is desired, the toner may be made from a black dye, such as a black dye such as carbon black or an amaplast black dye.
本発明のトナーに用いられる着色剤の添加量は幅広く採
用されるが、通常、トナー用結着樹脂100重早部に対
して1〜20重量部である。The amount of the colorant used in the toner of the present invention can be widely adopted, but it is usually 1 to 20 parts by weight based on 100 parts by weight of the toner binder resin.
トナーを一成分系埠像剤として用いる時には任意の磁性
体を添加することかでさる。When the toner is used as a one-component imaging agent, an arbitrary magnetic material may be added thereto.
使用できる磁性体としては、磁場によってその方向に強
く磁化する物質であり、好ましくは黒色で、1台・1脂
中に良く分散して化学的に安定であり、史に粒径として
は1μ以下の微粒子状のものか容易に得られることが望
ましく、マグネタイト(四三酸化鉄)が最も好ましい。The magnetic material that can be used is a material that is strongly magnetized in the direction of a magnetic field, preferably black in color, well dispersed in one unit/one fat, chemically stable, and with a particle size of 1μ or less. It is desirable that the material be easily obtained in the form of fine particles, and magnetite (triiron tetroxide) is the most preferred.
代表的な磁性又は磁化可能な材料としては、コバルト、
鉄、ニッケルのような金属ニアルミニウム、コバルト、
銅、鉄、鉛、マグネシウム、ニッケル、スズ、亜鉛、ア
ンチモン、ベリリウム、ビスマス、カドミウム、カルシ
ウム、マンカン、セレン、チタン、タングステン、バナ
ジウムのような金属の合金及びその混合物;酸化アルミ
ニウム、酸化鉄、酸化銅、酸化ニッケル、酸化亜鈍)、
酸化ブタン及び酸化マグネシウムのような金属酸化物を
含む金属化合物:チツ化バナジウム、チツ化クロムのよ
うな耐火性チッ化物;炭化タングステン及び炭化シリカ
のような炭化物;フェライト及びそれらの混合物が使用
される。これらの強磁性体は平均粒径が0.1〜1μ程
度のものが望ましく、トナー中に含有させる吊はトナー
用粘着樹脂成分100重ω部に対し約50〜500重量
部である事が望ましく、特に好ましくは樹脂成分100
重早部に対し80〜200申吊部でおる。Typical magnetic or magnetizable materials include cobalt,
Metals like iron, nickel, aluminum, cobalt,
Alloys and mixtures of metals such as copper, iron, lead, magnesium, nickel, tin, zinc, antimony, beryllium, bismuth, cadmium, calcium, mankan, selenium, titanium, tungsten, vanadium; aluminum oxide, iron oxide, oxide copper, nickel oxide, annealed oxide),
Metal compounds including metal oxides such as butane oxide and magnesium oxide; refractory nitrides such as vanadium nitride, chromium nitride; carbides such as tungsten carbide and silica carbide; ferrites and mixtures thereof are used. . These ferromagnetic materials preferably have an average particle size of about 0.1 to 1 μm, and the amount of ferromagnetic material contained in the toner is preferably about 50 to 500 parts by weight per 100 parts by weight of the adhesive resin component for toner. , particularly preferably resin component 100
It is 80 to 200 times lower than the heavy early part.
トナーには、その他電荷制御剤、流動化剤等を適宜添加
してもよい。Other charge control agents, fluidizing agents, etc. may be added to the toner as appropriate.
トナーはいわゆる練肉法、重合法等の任意の製造方法に
より製造される。The toner is manufactured by any manufacturing method such as the so-called kneading method and polymerization method.
練肉法とは、例えばトナー用結着樹脂、離型剤、着色剤
、電荷制御剤、磁性体等を混合し、溶融練肉、冷却、粉
砕し製造する方法である。The kneading method is a method of manufacturing by mixing, for example, a binder resin for toner, a mold release agent, a coloring agent, a charge control agent, a magnetic material, etc., melting the mixture, cooling it, and pulverizing it.
一方、重合法とは、トナー用結着樹脂の11量体に離型
剤、着色剤、電荷制御剤、磁性体等を混合し、例えば懸
濁重合により一挙にトナーを製造する方法である。On the other hand, the polymerization method is a method in which a release agent, a colorant, a charge control agent, a magnetic material, etc. are mixed with a 11-mer binder resin for toner, and a toner is produced all at once by, for example, suspension polymerization.
(3)−次転写工程
感光体ベルト上のトナー像は次にb方向に移動する中間
転写媒体2に、非静電的方法、すなわら支持ロール12
と押圧ロール13との間を感光体ベルトと中間転写ベル
トを重ねて通す方法によって一次転写される。(3)-Next transfer process The toner image on the photoreceptor belt is then transferred to the intermediate transfer medium 2 moving in the b direction by a non-electrostatic method, i.e. by the support roll 12.
The primary transfer is performed by passing the photoreceptor belt and the intermediate transfer belt overlappingly between the press roll 13 and the press roll 13 .
この−次転写で使用する中間転写媒体は、−次転写、二
次転写での転移率、画像部の抜け(中間転写媒体の凹部
に一次転写でトナー粒子が入り込み、二次転写で転写と
の接触部が不充分となり、最終画像上で白扱けとなる。The intermediate transfer medium used in this -next transfer has the following characteristics: -next transfer, transfer rate in the secondary transfer, omission of image areas (toner particles enter the recesses of the intermediate transfer medium in the primary transfer, The contact area will be insufficient and will appear white on the final image.
この現象は網点画像の場合ドツトのDIIlaxを低下
させ階調性を損なう原因となる。)、更に中間転写媒体
のクリーニングの容易さを考慮するとその表面の平滑性
か重要である。In the case of a halftone image, this phenomenon lowers the DIIlax of the dots and causes a loss of gradation. ), and considering the ease of cleaning the intermediate transfer medium, the smoothness of its surface is important.
実験によって、中間転写媒体の表面粗さか、深さ0.5
μ以上の凹凸の周波数2cycle/m以下、深さ3μ
以下で良好な結果をもたらすことか判明した。Experiments have shown that the surface roughness of the intermediate transfer medium or the depth of 0.5
Frequency of unevenness of μ or more: 2 cycles/m or less, depth: 3μ
It was found that the following gave good results.
このような表面粗さの中間転写媒体としては耐熱性樹脂
フィルム上に、各種のエラストマー、ゴム材料の層を設
けたものか用いられる。表面層の具体例を挙げると、東
芝シリコーンネ1製の、TSE387RTV、TSE3
88W、TSE389C(以−ヒ商品名)、信越化学社
製の、KI?271. KR272,KE 130.に
E136−V、 KE12RrV。As an intermediate transfer medium having such a rough surface, a heat-resistant resin film with layers of various elastomers or rubber materials is used. Specific examples of the surface layer include TSE387RTV and TSE3 manufactured by Toshiba Silicone 1.
88W, TSE389C (trade name), manufactured by Shin-Etsu Chemical Co., Ltd., KI? 271. KR272, KE 130. E136-V, KE12RrV.
にE17RTV、にE/12RTV、KE113RTV
、 KF1800ABCRTV等(以上商品名)、東し
シリコーン社製の、Sl+−780,5E9140.3
8850,5H748V、 5RX475V、5H16
03V等(以−ヒ商品名)、バイエル社製(7)EVW
−1018,EV−1840等(LX上商品名)、日本
ポリウレタン社製のコロネートC−4046,ニラポラ
ン4038等(以上商品名)などである。E17RTV, E/12RTV, KE113RTV
, KF1800ABCRTV, etc. (all above product names), manufactured by Toshi Silicone Co., Ltd., Sl+-780, 5E9140.3
8850, 5H748V, 5RX475V, 5H16
03V etc. (hereinafter referred to as product name), manufactured by Bayer (7) EVW
-1018, EV-1840, etc. (trade names on LX), Coronate C-4046, Niraporan 4038, etc. (trade names listed above) manufactured by Nippon Polyurethane Co., Ltd., and the like.
更に帯電防止の目的でカーボンブラック、金属粉を分散
させてもよい。Furthermore, carbon black or metal powder may be dispersed for the purpose of preventing static electricity.
一次転写工程では、非静電的に転写を行なう上で転写前
に除電器]1によって中間転写媒体の除電を行なう。In the primary transfer step, the transfer is performed non-electrostatically, and the intermediate transfer medium is neutralized by a static eliminator 1 before the transfer.
(4)二次転写定着工程
次に一次転写トナー像をC方向に移動する転写紙3を介
在させて加熱定着[1−ル15を支持ロール14に押圧
し転写定着を行う。(4) Secondary transfer fixing step Next, the primary transfer toner image is heated and fixed with the transfer paper 3 moving in the C direction interposed. [1-Rule 15 is pressed against the support roll 14 to transfer and fix the image.
この転写定着工程では、中間転写媒体上のトナー像を予
熱器9によって加熱し、また転写紙も予熱器16によっ
て加熱する。In this transfer fixing process, the toner image on the intermediate transfer medium is heated by a preheater 9, and the transfer paper is also heated by a preheater 16.
二次転写定着後の中間転写媒体はクリーニング装置10
によってクリーニングされて次のサイクルに備えられる
。The intermediate transfer medium after the secondary transfer and fixing is cleaned by a cleaning device 10.
is cleaned and prepared for the next cycle.
また−次転写後の感光体ベルトも除電器7で除電後クリ
ーニング装置8でクリーニングされ、次の接写リイクル
に移行する。Further, the photoreceptor belt after the next transfer is also cleaned by the cleaning device 8 after being neutralized by the static eliminator 7, and then transferred to the next close-up recycle.
[実施例] 以下、実施例および比較例を挙げて本発明を説明する。[Example] The present invention will be described below with reference to Examples and Comparative Examples.
実施例
感光体としてSe系感光体(表面粗さか、深さ0.5μ
以上の凹凸周波数1cycle/m、深さ0.5μ:5
LOAN叶にTAK[により測定)、露光系として富士
写真フィルム社製静電印刷マスター“ELP280”、
現像条1′Fとして、−成分磁性トナー(d 50=
4.8μ、d9o/d、o= 3.5.抵抗率: 10
3v/cmの電場で、1.4Nff/−で作成したトナ
ーディスクの値として2X103Ω・cm)を用いる磁
気ブラシ現像法を採用し、中間転写媒体として、シリコ
ーンRTV (信越化学社製、厚み100μ、表面粗
さが深さ0.5μ以上の凹凸周波数1CVC1e/繭、
深さ2.5μ)を用い、h0熱定着ロールの表面温度を
180 ’(1:とじて複写テストを行ったところ、網
点原稿の階調再現性にすぐれた高品質の複写画像か得ら
れた。The example photoreceptor was a Se-based photoreceptor (surface roughness or depth of 0.5 μm).
Above unevenness frequency 1 cycle/m, depth 0.5μ: 5
TAK [measured by LOAN Kano], Fuji Photo Film Co., Ltd.'s electrostatic printing master "ELP280" as the exposure system,
-component magnetic toner (d50=
4.8μ, d9o/d, o=3.5. Resistivity: 10
A magnetic brush development method was adopted using a toner disk (2X103Ωcm) created with an electric field of 3V/cm and 1.4Nff/-, and silicone RTV (manufactured by Shin-Etsu Chemical Co., Ltd., thickness 100μ, Concave and convex frequency 1CVC1e/cocoon with surface roughness of depth 0.5μ or more,
When a copying test was carried out using a 2.5μ depth) and a surface temperature of the h0 heat fixing roll of 180' (1:1), a high quality copy image with excellent gradation reproducibility of halftone originals was obtained. Ta.
比較例
感光体としてZnO系感光体(表面粗さが、深さ0.5
μ以上の凹凸周波数6 Cyc l e/m、深さ8μ
:〉、露光系としてレンズミラースキャン方式(roK
o )IAsTERFAX ) ヲ採用し、現像条件お
よび一次転写、二次転写定着条件は実施例と全く同じ条
件で複写テストを行なったところ、網点原稿のシャド一
部の漬れがa察され、また最大画像濃度(DmaX)が
低く、全体的に軟調な感じの画像がjqられた。A ZnO-based photoreceptor (surface roughness: 0.5 in depth) was used as a comparative example photoreceptor.
Concave and convex frequency of μ or more 6 Cycl e/m, depth 8μ
:〉, lens mirror scan method (roK
o)IAsTERFAX) When a copying test was conducted using the same developing conditions, primary transfer, and secondary transfer fixing conditions as in the example, it was observed that some shadows of the halftone original were soaked, and The maximum image density (DmaX) was low, and the image had a soft overall feel.
第3図に実施例および比較例の網点画像における階調性
(175線/インチの原稿濃度と複写画像温度との関係
)を示す。FIG. 3 shows the gradation (relationship between original density of 175 lines/inch and copy image temperature) in halftone images of Examples and Comparative Examples.
[発明の効果]
本発明は中間転写媒体を用いてトナー像を非静電的に一
旦一次転写した後、記録紙に転写定着する複写方法にお
いて、潜像形成、導電性トナーを用いる均一薄層現像、
−次転写、二次転写定着の一連のプロセスを組合わけて
、高品質の最終画像を17ることができる新規な複写方
法を提供したものである。[Effects of the Invention] The present invention relates to a copying method in which a toner image is first transferred non-electrostatically using an intermediate transfer medium, and then transferred and fixed onto a recording paper. developing,
- A novel copying method is provided which is capable of producing a high quality final image by combining a series of processes of secondary transfer and secondary transfer and fixing.
第1図は、本発明の複写方法における作像プロセスの説
明図、第2図は本発明の複写方法を実施するシステム例
の概要図、第3図は実施例および比較例の線点再現にお
ける階調性を示すグラフである。
図中符号:
1・・・感光体ベルト; 2・・・中間転写ベルト:3
・・・転写紙: 4・・・帯電器; 5・・・露光:6
・・・現像機ニア、11・・・除電器:8.10・・・
クリーニング装置; 9・・・トフー予熱器: 12゜
14・・・支持ロール: 13・・・押圧ロール;15
・・・IJ11熱ロール; 16・・・転写紙予熱器;
a、b、c・・・移動方向。
第1図((1)
第1図(b)
第1図(C)
第1図(d)
第1図(e)
第2図FIG. 1 is an explanatory diagram of the image forming process in the copying method of the present invention, FIG. 2 is a schematic diagram of an example of a system implementing the copying method of the present invention, and FIG. 3 is a diagram showing line point reproduction in the example and comparative example. It is a graph showing gradation. Symbols in the figure: 1... Photoreceptor belt; 2... Intermediate transfer belt: 3
...Transfer paper: 4...Charger; 5...Exposure: 6
...Developer near, 11...Static eliminator: 8.10...
Cleaning device; 9... Tofu preheater: 12° 14... Support roll: 13... Press roll; 15
...IJ11 heat roll; 16...transfer paper preheater;
a, b, c...Movement direction. Figure 1 ((1) Figure 1 (b) Figure 1 (C) Figure 1 (d) Figure 1 (e) Figure 2
Claims (1)
形成する工程、その静電潜像を導電性トナーにより均一
薄層状態で現像する工程、得られたトナー像を表面が平
滑な中間転写媒体に非静電的に転写する工程、中間転写
媒体上のトナー像を記録シートを介在させて加熱ロール
にて押圧し記録シートに転写定着する工程からなること
を特徴とする複写方法。 2)記録媒体表面粗さが、深さ0.5μ以上の凹凸の周
波数1cycle/m以下、深さ1μ以下である特許請
求の範囲第1項に記載の複写方法。 3)現像工程において記録媒体上に形成されるトナー層
の厚みが20μ以下である特許請求の範囲第1項記載の
複写方法。 4)中間転写媒体の表面粗さが、深さ0.5μ以上の凹
凸の周波数2cycle/mm以下、深さ3μ以下であ
る特許請求の範囲第1項に記載の複写方法。[Claims] 1) A step of forming an electrostatic latent image faithful to the original on a recording medium with a smooth surface, a step of developing the electrostatic latent image in a uniform thin layer with conductive toner, The toner image is transferred non-electrostatically to an intermediate transfer medium with a smooth surface, and the toner image on the intermediate transfer medium is transferred and fixed onto the recording sheet by being pressed with a heating roll with a recording sheet interposed. A copying method characterized by: 2) The copying method according to claim 1, wherein the surface roughness of the recording medium is such that the frequency of irregularities of 0.5 μm or more in depth is 1 cycle/m or less and the depth is 1 μm or less. 3) The copying method according to claim 1, wherein the thickness of the toner layer formed on the recording medium in the developing step is 20 μm or less. 4) The copying method according to claim 1, wherein the surface roughness of the intermediate transfer medium is such that the frequency of irregularities of 0.5 μm or more in depth is 2 cycles/mm or less and the depth is 3 μm or less.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP61177759A JPS6334571A (en) | 1986-07-30 | 1986-07-30 | Copying method |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP61177759A JPS6334571A (en) | 1986-07-30 | 1986-07-30 | Copying method |
Publications (1)
Publication Number | Publication Date |
---|---|
JPS6334571A true JPS6334571A (en) | 1988-02-15 |
Family
ID=16036631
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP61177759A Pending JPS6334571A (en) | 1986-07-30 | 1986-07-30 | Copying method |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS6334571A (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US7215912B2 (en) | 2004-03-19 | 2007-05-08 | Ricoh Company Limited | Intermediate transfer medium and image forming apparatus using the intermediate transfer medium |
Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5919980A (en) * | 1982-07-22 | 1984-02-01 | シ−・アイ・アイ・ハネウエル・ブル | Apparatus for removing excessive developer particle on surface of recording element |
JPS59202477A (en) * | 1983-05-04 | 1984-11-16 | Konishiroku Photo Ind Co Ltd | Recording device utilizing intermediate transfer body |
JPS59206855A (en) * | 1983-05-10 | 1984-11-22 | Konishiroku Photo Ind Co Ltd | Recorder |
JPS6136752A (en) * | 1984-07-30 | 1986-02-21 | Canon Inc | Recording medium of electrostatic recorder |
-
1986
- 1986-07-30 JP JP61177759A patent/JPS6334571A/en active Pending
Patent Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5919980A (en) * | 1982-07-22 | 1984-02-01 | シ−・アイ・アイ・ハネウエル・ブル | Apparatus for removing excessive developer particle on surface of recording element |
JPS59202477A (en) * | 1983-05-04 | 1984-11-16 | Konishiroku Photo Ind Co Ltd | Recording device utilizing intermediate transfer body |
JPS59206855A (en) * | 1983-05-10 | 1984-11-22 | Konishiroku Photo Ind Co Ltd | Recorder |
JPS6136752A (en) * | 1984-07-30 | 1986-02-21 | Canon Inc | Recording medium of electrostatic recorder |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US7215912B2 (en) | 2004-03-19 | 2007-05-08 | Ricoh Company Limited | Intermediate transfer medium and image forming apparatus using the intermediate transfer medium |
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