JPH04240660A - Method for fixing color copied image - Google Patents
Method for fixing color copied imageInfo
- Publication number
- JPH04240660A JPH04240660A JP3007064A JP706491A JPH04240660A JP H04240660 A JPH04240660 A JP H04240660A JP 3007064 A JP3007064 A JP 3007064A JP 706491 A JP706491 A JP 706491A JP H04240660 A JPH04240660 A JP H04240660A
- Authority
- JP
- Japan
- Prior art keywords
- toner
- resin
- molecular weight
- heating roller
- fixing
- 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 11
- 229920005989 resin Polymers 0.000 claims abstract description 18
- 239000011347 resin Substances 0.000 claims abstract description 18
- 239000011230 binding agent Substances 0.000 claims abstract description 9
- 230000003746 surface roughness Effects 0.000 claims abstract description 6
- 238000010438 heat treatment Methods 0.000 claims description 25
- 239000000155 melt Substances 0.000 claims description 10
- 230000000704 physical effect Effects 0.000 abstract description 2
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical group C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 9
- 230000000052 comparative effect Effects 0.000 description 8
- 229920001225 polyester resin Polymers 0.000 description 8
- 239000004645 polyester resin Substances 0.000 description 8
- 229920005792 styrene-acrylic resin Polymers 0.000 description 8
- 229920006026 co-polymeric resin Polymers 0.000 description 6
- 239000003086 colorant Substances 0.000 description 6
- 238000011156 evaluation Methods 0.000 description 6
- 229920001909 styrene-acrylic polymer Polymers 0.000 description 6
- OFOBLEOULBTSOW-UHFFFAOYSA-N Malonic acid Chemical compound OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 5
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 description 4
- 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 4
- 239000000049 pigment Substances 0.000 description 4
- 229920002379 silicone rubber Polymers 0.000 description 4
- 239000004945 silicone rubber Substances 0.000 description 4
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 3
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 3
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 3
- 239000003795 chemical substances by application Substances 0.000 description 3
- 230000003247 decreasing effect Effects 0.000 description 3
- ARCGXLSVLAOJQL-UHFFFAOYSA-N trimellitic acid Chemical compound OC(=O)C1=CC=C(C(O)=O)C(C(O)=O)=C1 ARCGXLSVLAOJQL-UHFFFAOYSA-N 0.000 description 3
- UAJRSHJHFRVGMG-UHFFFAOYSA-N 1-ethenyl-4-methoxybenzene Chemical compound COC1=CC=C(C=C)C=C1 UAJRSHJHFRVGMG-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
- SOGAXMICEFXMKE-UHFFFAOYSA-N Butylmethacrylate Chemical compound CCCCOC(=O)C(C)=C SOGAXMICEFXMKE-UHFFFAOYSA-N 0.000 description 2
- VZCYOOQTPOCHFL-OWOJBTEDSA-N Fumaric acid Chemical compound OC(=O)\C=C\C(O)=O VZCYOOQTPOCHFL-OWOJBTEDSA-N 0.000 description 2
- BAPJBEWLBFYGME-UHFFFAOYSA-N Methyl acrylate Chemical compound COC(=O)C=C BAPJBEWLBFYGME-UHFFFAOYSA-N 0.000 description 2
- 239000004809 Teflon Substances 0.000 description 2
- 229920006362 Teflon® Polymers 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
- 239000000654 additive Substances 0.000 description 2
- WNLRTRBMVRJNCN-UHFFFAOYSA-N adipic acid Chemical compound OC(=O)CCCCC(O)=O WNLRTRBMVRJNCN-UHFFFAOYSA-N 0.000 description 2
- WTNDADANUZETTI-UHFFFAOYSA-N cyclohexane-1,2,4-tricarboxylic acid Chemical compound OC(=O)C1CCC(C(O)=O)C(C(O)=O)C1 WTNDADANUZETTI-UHFFFAOYSA-N 0.000 description 2
- 230000007547 defect Effects 0.000 description 2
- QQVIHTHCMHWDBS-UHFFFAOYSA-N isophthalic acid Chemical compound OC(=O)C1=CC=CC(C(O)=O)=C1 QQVIHTHCMHWDBS-UHFFFAOYSA-N 0.000 description 2
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 description 2
- 239000002245 particle Substances 0.000 description 2
- XNGIFLGASWRNHJ-UHFFFAOYSA-N phthalic acid Chemical compound OC(=O)C1=CC=CC=C1C(O)=O XNGIFLGASWRNHJ-UHFFFAOYSA-N 0.000 description 2
- 229920005862 polyol Polymers 0.000 description 2
- 150000003077 polyols Chemical class 0.000 description 2
- YPFDHNVEDLHUCE-UHFFFAOYSA-N propane-1,3-diol Chemical compound OCCCO YPFDHNVEDLHUCE-UHFFFAOYSA-N 0.000 description 2
- NHARPDSAXCBDDR-UHFFFAOYSA-N propyl 2-methylprop-2-enoate Chemical compound CCCOC(=O)C(C)=C NHARPDSAXCBDDR-UHFFFAOYSA-N 0.000 description 2
- CXMXRPHRNRROMY-UHFFFAOYSA-N sebacic acid Chemical compound OC(=O)CCCCCCCCC(O)=O CXMXRPHRNRROMY-UHFFFAOYSA-N 0.000 description 2
- 229920002545 silicone oil Polymers 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
- 238000002834 transmittance Methods 0.000 description 2
- XVOUMQNXTGKGMA-OWOJBTEDSA-N (E)-glutaconic acid Chemical compound OC(=O)C\C=C\C(O)=O XVOUMQNXTGKGMA-OWOJBTEDSA-N 0.000 description 1
- BJQFWAQRPATHTR-UHFFFAOYSA-N 1,2-dichloro-4-ethenylbenzene Chemical compound ClC1=CC=C(C=C)C=C1Cl BJQFWAQRPATHTR-UHFFFAOYSA-N 0.000 description 1
- QOVCUELHTLHMEN-UHFFFAOYSA-N 1-butyl-4-ethenylbenzene Chemical compound CCCCC1=CC=C(C=C)C=C1 QOVCUELHTLHMEN-UHFFFAOYSA-N 0.000 description 1
- KTZVZZJJVJQZHV-UHFFFAOYSA-N 1-chloro-4-ethenylbenzene Chemical compound ClC1=CC=C(C=C)C=C1 KTZVZZJJVJQZHV-UHFFFAOYSA-N 0.000 description 1
- DMADTXMQLFQQII-UHFFFAOYSA-N 1-decyl-4-ethenylbenzene Chemical compound CCCCCCCCCCC1=CC=C(C=C)C=C1 DMADTXMQLFQQII-UHFFFAOYSA-N 0.000 description 1
- WJNKJKGZKFOLOJ-UHFFFAOYSA-N 1-dodecyl-4-ethenylbenzene Chemical compound CCCCCCCCCCCCC1=CC=C(C=C)C=C1 WJNKJKGZKFOLOJ-UHFFFAOYSA-N 0.000 description 1
- 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
- NVZWEEGUWXZOKI-UHFFFAOYSA-N 1-ethenyl-2-methylbenzene Chemical compound CC1=CC=CC=C1C=C NVZWEEGUWXZOKI-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
- LCNAQVGAHQVWIN-UHFFFAOYSA-N 1-ethenyl-4-hexylbenzene Chemical compound CCCCCCC1=CC=C(C=C)C=C1 LCNAQVGAHQVWIN-UHFFFAOYSA-N 0.000 description 1
- LUWBJDCKJAZYKZ-UHFFFAOYSA-N 1-ethenyl-4-nonylbenzene Chemical compound CCCCCCCCCC1=CC=C(C=C)C=C1 LUWBJDCKJAZYKZ-UHFFFAOYSA-N 0.000 description 1
- HLRQDIVVLOCZPH-UHFFFAOYSA-N 1-ethenyl-4-octylbenzene Chemical compound CCCCCCCCC1=CC=C(C=C)C=C1 HLRQDIVVLOCZPH-UHFFFAOYSA-N 0.000 description 1
- QEDJMOONZLUIMC-UHFFFAOYSA-N 1-tert-butyl-4-ethenylbenzene Chemical compound CC(C)(C)C1=CC=C(C=C)C=C1 QEDJMOONZLUIMC-UHFFFAOYSA-N 0.000 description 1
- JAHNSTQSQJOJLO-UHFFFAOYSA-N 2-(3-fluorophenyl)-1h-imidazole Chemical compound FC1=CC=CC(C=2NC=CN=2)=C1 JAHNSTQSQJOJLO-UHFFFAOYSA-N 0.000 description 1
- JKNCOURZONDCGV-UHFFFAOYSA-N 2-(dimethylamino)ethyl 2-methylprop-2-enoate Chemical compound CN(C)CCOC(=O)C(C)=C JKNCOURZONDCGV-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
- WHBAYNMEIXUTJV-UHFFFAOYSA-N 2-chloroethyl prop-2-enoate Chemical compound ClCCOC(=O)C=C WHBAYNMEIXUTJV-UHFFFAOYSA-N 0.000 description 1
- WDQMWEYDKDCEHT-UHFFFAOYSA-N 2-ethylhexyl 2-methylprop-2-enoate Chemical compound CCCCC(CC)COC(=O)C(C)=C WDQMWEYDKDCEHT-UHFFFAOYSA-N 0.000 description 1
- 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
- JLBJTVDPSNHSKJ-UHFFFAOYSA-N 4-Methylstyrene Chemical compound CC1=CC=C(C=C)C=C1 JLBJTVDPSNHSKJ-UHFFFAOYSA-N 0.000 description 1
- JTHZUSWLNCPZLX-UHFFFAOYSA-N 6-fluoro-3-methyl-2h-indazole Chemical compound FC1=CC=C2C(C)=NNC2=C1 JTHZUSWLNCPZLX-UHFFFAOYSA-N 0.000 description 1
- HRPVXLWXLXDGHG-UHFFFAOYSA-N Acrylamide Chemical compound NC(=O)C=C HRPVXLWXLXDGHG-UHFFFAOYSA-N 0.000 description 1
- NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 description 1
- JIGUQPWFLRLWPJ-UHFFFAOYSA-N Ethyl acrylate Chemical compound CCOC(=O)C=C JIGUQPWFLRLWPJ-UHFFFAOYSA-N 0.000 description 1
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical group [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 1
- VVQNEPGJFQJSBK-UHFFFAOYSA-N Methyl methacrylate Chemical compound COC(=O)C(C)=C VVQNEPGJFQJSBK-UHFFFAOYSA-N 0.000 description 1
- GYCMBHHDWRMZGG-UHFFFAOYSA-N Methylacrylonitrile Chemical compound CC(=C)C#N GYCMBHHDWRMZGG-UHFFFAOYSA-N 0.000 description 1
- KDYFGRWQOYBRFD-UHFFFAOYSA-N Succinic acid Natural products OC(=O)CCC(O)=O KDYFGRWQOYBRFD-UHFFFAOYSA-N 0.000 description 1
- YIMQCDZDWXUDCA-UHFFFAOYSA-N [4-(hydroxymethyl)cyclohexyl]methanol Chemical compound OCC1CCC(CO)CC1 YIMQCDZDWXUDCA-UHFFFAOYSA-N 0.000 description 1
- MZVQCMJNVPIDEA-UHFFFAOYSA-N [CH2]CN(CC)CC Chemical group [CH2]CN(CC)CC MZVQCMJNVPIDEA-UHFFFAOYSA-N 0.000 description 1
- 229920006243 acrylic copolymer Polymers 0.000 description 1
- 239000001361 adipic acid Substances 0.000 description 1
- 235000011037 adipic acid Nutrition 0.000 description 1
- AZDRQVAHHNSJOQ-UHFFFAOYSA-N alumane Chemical group [AlH3] AZDRQVAHHNSJOQ-UHFFFAOYSA-N 0.000 description 1
- 239000000038 blue colorant Substances 0.000 description 1
- CDQSJQSWAWPGKG-UHFFFAOYSA-N butane-1,1-diol Chemical compound CCCC(O)O CDQSJQSWAWPGKG-UHFFFAOYSA-N 0.000 description 1
- LOGBRYZYTBQBTB-UHFFFAOYSA-N butane-1,2,4-tricarboxylic acid Chemical compound OC(=O)CCC(C(O)=O)CC(O)=O LOGBRYZYTBQBTB-UHFFFAOYSA-N 0.000 description 1
- KDYFGRWQOYBRFD-NUQCWPJISA-N butanedioic acid Chemical compound O[14C](=O)CC[14C](O)=O KDYFGRWQOYBRFD-NUQCWPJISA-N 0.000 description 1
- CQEYYJKEWSMYFG-UHFFFAOYSA-N butyl acrylate Chemical compound CCCCOC(=O)C=C CQEYYJKEWSMYFG-UHFFFAOYSA-N 0.000 description 1
- HNEGQIOMVPPMNR-IHWYPQMZSA-N citraconic acid Chemical compound OC(=O)C(/C)=C\C(O)=O HNEGQIOMVPPMNR-IHWYPQMZSA-N 0.000 description 1
- 229940018557 citraconic acid Drugs 0.000 description 1
- 210000000078 claw Anatomy 0.000 description 1
- 239000000306 component Substances 0.000 description 1
- XCJYREBRNVKWGJ-UHFFFAOYSA-N copper(II) phthalocyanine Chemical compound [Cu+2].C12=CC=CC=C2C(N=C2[N-]C(C3=CC=CC=C32)=N2)=NC1=NC([C]1C=CC=CC1=1)=NC=1N=C1[C]3C=CC=CC3=C2[N-]1 XCJYREBRNVKWGJ-UHFFFAOYSA-N 0.000 description 1
- 230000007423 decrease Effects 0.000 description 1
- 230000006866 deterioration Effects 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
- 239000000975 dye Substances 0.000 description 1
- 229920001971 elastomer Polymers 0.000 description 1
- SUPCQIBBMFXVTL-UHFFFAOYSA-N ethyl 2-methylprop-2-enoate Chemical compound CCOC(=O)C(C)=C SUPCQIBBMFXVTL-UHFFFAOYSA-N 0.000 description 1
- 239000001530 fumaric acid Substances 0.000 description 1
- 238000004898 kneading Methods 0.000 description 1
- PBOSTUDLECTMNL-UHFFFAOYSA-N lauryl acrylate Chemical compound CCCCCCCCCCCCOC(=O)C=C PBOSTUDLECTMNL-UHFFFAOYSA-N 0.000 description 1
- 235000010187 litholrubine BK Nutrition 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
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- HNEGQIOMVPPMNR-NSCUHMNNSA-N mesaconic acid Chemical compound OC(=O)C(/C)=C/C(O)=O HNEGQIOMVPPMNR-NSCUHMNNSA-N 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- AWJZTPWDQYFQPQ-UHFFFAOYSA-N methyl 2-chloroprop-2-enoate Chemical compound COC(=O)C(Cl)=C AWJZTPWDQYFQPQ-UHFFFAOYSA-N 0.000 description 1
- YLGXILFCIXHCMC-JHGZEJCSSA-N methyl cellulose Chemical compound COC1C(OC)C(OC)C(COC)O[C@H]1O[C@H]1C(OC)C(OC)C(OC)OC1COC YLGXILFCIXHCMC-JHGZEJCSSA-N 0.000 description 1
- LVHBHZANLOWSRM-UHFFFAOYSA-N methylenebutanedioic acid Natural products OC(=O)CC(=C)C(O)=O LVHBHZANLOWSRM-UHFFFAOYSA-N 0.000 description 1
- HNEGQIOMVPPMNR-UHFFFAOYSA-N methylfumaric acid Natural products OC(=O)C(C)=CC(O)=O HNEGQIOMVPPMNR-UHFFFAOYSA-N 0.000 description 1
- 239000006082 mold release agent Substances 0.000 description 1
- 239000000178 monomer Substances 0.000 description 1
- HMZGPNHSPWNGEP-UHFFFAOYSA-N octadecyl 2-methylprop-2-enoate Chemical compound CCCCCCCCCCCCCCCCCCOC(=O)C(C)=C HMZGPNHSPWNGEP-UHFFFAOYSA-N 0.000 description 1
- NZIDBRBFGPQCRY-UHFFFAOYSA-N octyl 2-methylprop-2-enoate Chemical compound CCCCCCCCOC(=O)C(C)=C NZIDBRBFGPQCRY-UHFFFAOYSA-N 0.000 description 1
- ANISOHQJBAQUQP-UHFFFAOYSA-N octyl prop-2-enoate Chemical compound CCCCCCCCOC(=O)C=C ANISOHQJBAQUQP-UHFFFAOYSA-N 0.000 description 1
- HDBWAWNLGGMZRQ-UHFFFAOYSA-N p-Vinylbiphenyl Chemical compound C1=CC(C=C)=CC=C1C1=CC=CC=C1 HDBWAWNLGGMZRQ-UHFFFAOYSA-N 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
- QIWKUEJZZCOPFV-UHFFFAOYSA-N phenyl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OC1=CC=CC=C1 QIWKUEJZZCOPFV-UHFFFAOYSA-N 0.000 description 1
- WRAQQYDMVSCOTE-UHFFFAOYSA-N phenyl prop-2-enoate Chemical compound C=CC(=O)OC1=CC=CC=C1 WRAQQYDMVSCOTE-UHFFFAOYSA-N 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 229920001343 polytetrafluoroethylene Polymers 0.000 description 1
- 239000004810 polytetrafluoroethylene Substances 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- PNXMTCDJUBJHQJ-UHFFFAOYSA-N propyl prop-2-enoate Chemical compound CCCOC(=O)C=C PNXMTCDJUBJHQJ-UHFFFAOYSA-N 0.000 description 1
- 238000010298 pulverizing process Methods 0.000 description 1
- 239000001062 red colorant Substances 0.000 description 1
- 230000003578 releasing effect Effects 0.000 description 1
- 238000004904 shortening Methods 0.000 description 1
- 230000008961 swelling Effects 0.000 description 1
- ZIBGPFATKBEMQZ-UHFFFAOYSA-N triethylene glycol Chemical compound OCCOCCOCCO ZIBGPFATKBEMQZ-UHFFFAOYSA-N 0.000 description 1
Landscapes
- Developing Agents For Electrophotography (AREA)
- Fixing For Electrophotography (AREA)
- Color Electrophotography (AREA)
Abstract
Description
【0001】0001
【産業上の利用分野】本発明はカラー複写画像の定着方
法に関する。BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a method for fixing color copy images.
【0002】0002
【従来の技術】従来より、カラー複写機における複写画
像の定着は、定着されたトナー自体が優れた透光性、例
えばOHPシート上のカラートナー画像の透光性(以下
、OHP透光性という)と同程度の透光性を必要とする
。この優れた透光性を確保するために、低溶融粘度でシ
ャープメルトのトナーをシリコーンゴム系加熱ローラに
用いるシステムでなされている。なお、このOHP透光
性の確保には、表面平滑性の高い加熱ローラを使用して
トナー画像の表面を均一な面とすることを必要とする。2. Description of the Related Art Conventionally, in the fixation of copied images in color copying machines, the fixed toner itself has excellent translucency, for example, the translucency of color toner images on OHP sheets (hereinafter referred to as OHP translucency). ) requires the same level of translucency. In order to ensure this excellent light transmittance, a system is used in which a sharp melt toner with a low melt viscosity is used in a silicone rubber heating roller. In order to ensure this OHP transparency, it is necessary to use a heating roller with a high surface smoothness to make the surface of the toner image uniform.
【0003】また、上記システムでは、加熱ローラ表面
をシリコーンゴムで構成するとともに低溶融粘度のトナ
ーを使用するので、トナーが加熱ローラ表面に付着して
オフセットが発生しやすい。このため、加熱ローラ表面
に、シリコーンゴムとの親和性が大きく比較的安価なシ
リコーンオイルなどの多量の離型剤を塗布する必要があ
る。Furthermore, in the above system, the surface of the heating roller is made of silicone rubber and a toner with a low melting viscosity is used, so that the toner easily adheres to the surface of the heating roller and offset occurs. Therefore, it is necessary to apply a large amount of a mold release agent such as silicone oil, which has a high affinity with silicone rubber and is relatively inexpensive, to the surface of the heating roller.
【0004】0004
【発明が解決しようとする課題】ところが、上記従来の
システムでは、低溶融粘度でシャープメルトのトナーを
使用しているので、トナーの機械的強度が低く、またト
ナーの凝集力が急に低下する。このため、トナーと記録
紙との定着性が低下したり、トナーと加熱ローラとの離
型性が低下してオフセットが発生しやすいといった問題
がある。[Problems to be Solved by the Invention] However, since the above-mentioned conventional system uses a sharp melt toner with a low melt viscosity, the mechanical strength of the toner is low and the cohesive force of the toner suddenly decreases. . For this reason, there are problems in that the fixing property between the toner and the recording paper is reduced, and the releasing property between the toner and the heating roller is reduced, making it easy for offset to occur.
【0005】また、離型性をよくするために多量のシリ
コーンオイルを使用しているため、オイル膨潤、オイル
によりゴム劣化が発生して、加熱ローラの寿命が短くな
るという問題もある。ところで、白黒用複写機において
主流をなすテフロンローラ定着システムは、テフロンが
トナーとの離型性に優れるため、離型剤をローラ表面に
塗布する必要がない。このため、上記オイルによる問題
が発生することもなく、加熱ローラの寿命の点からは有
利である。[0005] Furthermore, since a large amount of silicone oil is used to improve mold releasability, there is also the problem that oil swelling and rubber deterioration occur due to the oil, shortening the life of the heating roller. By the way, in the Teflon roller fixing system that is the mainstream in black-and-white copying machines, there is no need to apply a release agent to the roller surface because Teflon has excellent release properties from toner. Therefore, the problem caused by the oil does not occur, which is advantageous in terms of the life of the heating roller.
【0006】本発明は上記実情に鑑みてなされたもので
あり、その技術課題は、耐久面で有利なフッ素樹脂系の
加熱ローラを用いてOHP透光性を確保することのでき
るカラー複写画像の定着方法を提供することにある。The present invention has been made in view of the above-mentioned circumstances, and its technical problem is to create a color copy image that can ensure OHP transparency using a fluororesin-based heating roller that is advantageous in terms of durability. The purpose is to provide a fixation method.
【0007】[0007]
【課題を解決するための手段】本発明のカラー画像の定
着方法は、表面がフッ素樹脂よりなりRz3.0μm以
下の表面粗さをもつ加熱ローラ、及び該加熱ローラに圧
接する加圧ローラ間にトナー画像を保持する記録紙を該
トナー画像面が該加熱ローラに面するように通過させる
ことにより該トナー画像を該記録紙上に定着させるカラ
ー複写画像の定着方法において、100℃における溶融
粘度が5×105 〜3×106 poise 、分子
量分布(Mw /Mn 、Mw :重量平均分子量、M
n :数平均分子量)が45以上、数平均分子量(Mn
)が1000〜4000である樹脂をバインダ成分と
して含むカラートナーを使用することを特徴とするもの
である。[Means for Solving the Problems] The color image fixing method of the present invention includes a heating roller whose surface is made of fluororesin and has a surface roughness of Rz 3.0 μm or less, and a pressure roller that is in pressure contact with the heating roller. In a color copy image fixing method in which the toner image is fixed on the recording paper by passing the recording paper holding the toner image so that the toner image side faces the heating roller, the melt viscosity at 100°C is 5. ×105 to 3×106 poise, molecular weight distribution (Mw/Mn, Mw: weight average molecular weight, M
n: number average molecular weight) is 45 or more, number average molecular weight (Mn
) is from 1,000 to 4,000 as a binder component.
【0008】上記カラートナーのバインダ成分となる樹
脂は、スチレン−アクリル系共重合樹脂、ポリエステル
系樹脂とすることができる。スチレン−アクリル系共重
合樹脂とポリエステル系樹脂とを比較すると、両者が同
じ溶融粘度の場合、耐熱性、樹脂の機械的強度の点でポ
リエステル系樹脂の方が優れている。このため、トナー
樹脂としてはポリエステル系樹脂を用いることが好まし
い。なお、スチレン−アクリル系共重合樹脂を使用する
場合は、上記数平均分子量(Mn )を3000〜40
00とすることが好ましい。また、ポリエステル系樹脂
を使用する場合は、数平均分子量(Mn )を1000
〜4000とすることができる。なお、ポリエステル系
樹脂を用いて数平均分子量(Mn )を3000〜40
00とすると、特に樹脂の機械的強度を確保することが
可能となる。The resin serving as the binder component of the color toner can be a styrene-acrylic copolymer resin or a polyester resin. When comparing a styrene-acrylic copolymer resin and a polyester resin, when both have the same melt viscosity, the polyester resin is superior in terms of heat resistance and mechanical strength of the resin. For this reason, it is preferable to use a polyester resin as the toner resin. In addition, when using styrene-acrylic copolymer resin, the above number average molecular weight (Mn) is 3000 to 40.
It is preferable to set it to 00. In addition, when using polyester resin, the number average molecular weight (Mn) should be 1000.
~4000. In addition, using polyester resin, the number average molecular weight (Mn) is 3000 to 40.
When it is set to 00, it becomes possible to particularly ensure the mechanical strength of the resin.
【0009】上記スチレン−アクリル系共重合樹脂を構
成するスチレン系モノマーとしては、例えば、スチレン
、o−メチルスチレン、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−n−ブチルスチレン、p−tert−ブチ
ルスチレン、p−n−ヘキシルスチレン、p−n−オク
チルスチレン、p−n−ノニルスチレン、p−n−デシ
ルスチレン、p−n−ドデシルスチレン、p−メトキシ
スチレン、p−フェニルスチレン、p−クロルスチレン
、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、その中でもスチレンが最も好ましい。Examples of the styrene monomer constituting the styrene-acrylic copolymer resin include styrene, o-methylstyrene, m-methylstyrene, p-methylstyrene, p-ethylstyrene, and 2,4-dimethylstyrene. , p-n-butylstyrene, p-tert-butylstyrene, p-n-hexylstyrene, p-n-octylstyrene, p-n-nonylstyrene, p-n-decylstyrene, p-n-dodecylstyrene, Examples include styrene and its derivatives, such as p-methoxystyrene, p-phenylstyrene, p-chlorostyrene, and 3,4-dichlorostyrene, among which styrene is most preferred.
【0010】上記スチレン−アクリル系共重合樹脂を構
成するアクリル系モノマーとしては、アクリル酸、アク
リル酸メチル、アクリル酸エチル、アクリル酸n−ブチ
ル、アクリル酸イソブチル、アクリル酸プロピル、アク
リル酸n−オクチル、アクリル酸ドデシル、アクリル酸
2−エチルヘキシル、アクリル酸ステアリル、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
アクリル酸メチル等のアクリル酸及びその誘導体、メタ
クリル酸、メタクリル酸メチル、メタクリル酸エチル、
メタクリル酸プロピル、メタクリル酸n−ブチル、メタ
クリル酸イソブチル、メタクリル酸プロピル、メタクリ
ル酸n−オクチル、メタクリル酸ドデシル、メタクリル
酸2−エチルヘキシル、メタクリル酸ステアリル、メタ
クリル酸フェニル、メタクリル酸ジメチルアミノエチル
、メタクリル酸ジエチルアミノエチル等のメタクリル酸
及びその誘導体、アクリロニトリル、メタクリロニトリ
ル、アクリルアミドなどのような(メタ)アクリル酸誘
導体等を挙げることができる。The acrylic monomers constituting the styrene-acrylic copolymer resin include acrylic acid, methyl acrylate, ethyl acrylate, n-butyl acrylate, isobutyl acrylate, propyl acrylate, and n-octyl acrylate. , acrylic acid and its derivatives such as dodecyl acrylate, 2-ethylhexyl acrylate, stearyl acrylate, 2-chloroethyl acrylate, phenyl acrylate, methyl α-chloroacrylate, methacrylic acid, methyl methacrylate, ethyl methacrylate,
Propyl methacrylate, n-butyl methacrylate, isobutyl methacrylate, propyl methacrylate, n-octyl methacrylate, dodecyl methacrylate, 2-ethylhexyl methacrylate, stearyl methacrylate, phenyl methacrylate, dimethylaminoethyl methacrylate, methacrylic acid Examples include methacrylic acid and its derivatives such as diethylaminoethyl, (meth)acrylic acid derivatives such as acrylonitrile, methacrylonitrile, acrylamide, and the like.
【0011】上記ポリエステル樹脂は、例えばポリオー
ル成分とジカルボン酸から合成されるが、ポリオール成
分としては、エチレングリコール、トリエチレングリコ
ール、1,2−プロピレングリコール、1,3−プロピ
レングリコール、1,4−ブタンジオール、1,4−ビ
ス(ヒドロキシメチル)シクロヘキサン、ビスフェノー
ルA、水素添加ビスフェノールA、ポリオキシエチレン
化ビスフェノールA等が使用でき、またジカルボン酸成
分としては、マレイン酸、フマール酸、メサコニン酸、
シトラコン酸、イタコン酸、グルタコン酸、フタール酸
、イソフタール酸、テレフタール酸、コハク酸、アジピ
ン酸、セバチン酸、マロン酸、1,2,4−ベンゼント
リカルボン酸、1,2,5−ベンゼントリカルボン酸、
1,2,4−シクロヘキサントリカルボン酸、1,2,
5−シクロヘキサントリカルボン酸、1,2,4−ブタ
ントリカルボン酸、1,3−ジカルボキシ−2−メチル
−2−メチルカルボキシプロパンテトラ(メチルカルボ
キシ)メタン等が使用できる。The above polyester resin is synthesized from, for example, a polyol component and dicarboxylic acid, and the polyol component includes ethylene glycol, triethylene glycol, 1,2-propylene glycol, 1,3-propylene glycol, and 1,4-propylene glycol. Butanediol, 1,4-bis(hydroxymethyl)cyclohexane, bisphenol A, hydrogenated bisphenol A, polyoxyethylated bisphenol A, etc. can be used, and as dicarboxylic acid components, maleic acid, fumaric acid, mesaconic acid,
Citraconic acid, itaconic acid, glutaconic acid, phthalic acid, isophthalic acid, terephthalic acid, succinic acid, adipic acid, sebacic acid, malonic acid, 1,2,4-benzenetricarboxylic acid, 1,2,5-benzenetricarboxylic acid,
1,2,4-cyclohexanetricarboxylic acid, 1,2,
5-cyclohexanetricarboxylic acid, 1,2,4-butanetricarboxylic acid, 1,3-dicarboxy-2-methyl-2-methylcarboxypropanetetra(methylcarboxy)methane, etc. can be used.
【0012】また、上記カラートナーに使用される着色
剤としては、例えば、黄色着色剤としてC.I.ピグメ
ントイエロー12、C.I.ピグメントイエロー13等
を、赤色着色剤としC.I.ピグメントレッド122、
C.I.ピグメントレッド57:1等、青色着色剤とし
てC.I.ピグメントブルー15等を挙げることができ
るが、それらの着色剤に限定されることなく、従来透光
性カラートナーに用いられている各色の顔料、染料等を
用いることができる。なお、上記カラートナーには着色
剤以外に、帯電制御剤等の所望の添加剤を添加してもよ
い。そして、これらの着色剤、その他の必要な添加剤の
添加量は、従来と同様とすることができる。[0012] Further, as the coloring agent used in the above color toner, for example, C.I. I. Pigment Yellow 12, C. I. Pigment Yellow 13 etc. as a red colorant and C.I. I. pigment red 122,
C. I. Pigment Red 57:1, C.I. as a blue colorant. I. Pigment Blue 15 and the like can be mentioned, but the colorant is not limited to these, and pigments, dyes, etc. of various colors conventionally used in translucent color toners can be used. In addition to the coloring agent, desired additives such as a charge control agent may be added to the color toner. The amounts of these colorants and other necessary additives can be the same as conventional ones.
【0013】上記トナーは、混練、粉砕法等で通常、平
均粒径が4〜25μmのトナーとして調製される。なお
、本発明の定着方法は、OHP透光性確保、及び高耐久
性の要求に応えるために、表面平滑性が高い(Rz3.
0μm以下)フッ素樹脂系の加熱ローラを用いる。[0013] The above-mentioned toner is usually prepared as a toner having an average particle size of 4 to 25 μm by kneading, pulverization, or the like. Note that the fixing method of the present invention has high surface smoothness (Rz3.
(0 μm or less) Use a fluororesin heating roller.
【0014】[0014]
【作用】本発明のカラー画像の定着方法では、使用する
カラートナーのバインダ成分となる樹脂の分子量分布が
45以上と極めて広範囲である。これにより、離型性を
確保してオフセットを防止するために及び樹脂の凝集力
を確保してトナーの定着強度を維持するために高分子側
を広げつつ、低溶融粘度のものとしてOHP透光性を確
保するために全体としては低分子化される。なお、10
0℃での溶融粘度が5×105 poise より小さ
い場合、又は樹脂としてスチレン−アクリル系共重合樹
脂を用いた場合の数平均分子量が3000より小さいか
若しは樹脂としてポリエステル系樹脂を用いた場合の数
平均分子量が1000より小さい場合は、樹脂の凝集力
が確保できず定着性が低下するとともに、離型性が悪化
して耐オフセット性が低下する。また、100℃での溶
融粘度が3×106 poise より大きい場合、又
は数平均分子量が4000より大きい場合は、OHP透
光性を確保することができない。[Operation] In the color image fixing method of the present invention, the molecular weight distribution of the resin serving as the binder component of the color toner used is over a very wide range of 45 or more. As a result, the polymer side is widened in order to ensure mold releasability and prevent offset, and to ensure the cohesive force of the resin and maintain the fixing strength of the toner. In order to ensure its properties, the overall molecular weight is reduced. In addition, 10
When the melt viscosity at 0°C is less than 5 x 105 poise, or when a styrene-acrylic copolymer resin is used as the resin, the number average molecular weight is less than 3000, or when a polyester resin is used as the resin. If the number average molecular weight is less than 1000, the cohesive force of the resin cannot be ensured, resulting in lower fixing properties, as well as poorer releasability and lower offset resistance. Further, when the melt viscosity at 100° C. is larger than 3×10 6 poise or when the number average molecular weight is larger than 4000, OHP translucency cannot be ensured.
【0015】なお、分子量分布が47であるスチレン−
アクリル系共重合樹脂の100℃での溶融粘度と数平均
分子量との関係を図2に示す。本発明のカラー画像の定
着方法は、このように物性が規定されたトナー樹脂をバ
インダ成分としてもつカラートナーを使用するので、O
HP透光性、定着性及び耐オフセット性を確保すること
ができる。[0015] Furthermore, styrene having a molecular weight distribution of 47
FIG. 2 shows the relationship between the melt viscosity at 100° C. and the number average molecular weight of the acrylic copolymer resin. The color image fixing method of the present invention uses a color toner having a toner resin with defined physical properties as a binder component.
HP transparency, fixing properties, and offset resistance can be ensured.
【0016】[0016]
【実施例】以下、本発明の実施例を説明する。(実施例
1)スチレン−アクリル樹脂(Mn ≒3500、Mw
/Mn =47)を100部、着色剤(大日精化製、
Seikafast Red.8040)を5部、荷
電制御剤(オリエント化学製、ボントロンE−81)を
2部、低分子量PPワックス(三洋化成製、ビスコール
330P)を4部の組成分を三本ロールミルで加熱混練
後、粉砕、分級して粒径12μmのカラートナーを得た
。[Examples] Examples of the present invention will be described below. (Example 1) Styrene-acrylic resin (Mn≒3500, Mw
/Mn = 47), 100 parts of colorant (manufactured by Dainichiseika,
Seikafast Red. 8040), 2 parts of a charge control agent (Bontron E-81, manufactured by Orient Chemical Co., Ltd.), and 4 parts of low molecular weight PP wax (Viscol 330P, manufactured by Sanyo Chemical Co., Ltd.) were heated and kneaded in a three-roll mill. The powder was crushed and classified to obtain a color toner having a particle size of 12 μm.
【0017】このトナーを降下式フローテスタ溶融粘度
測定器にて100℃の溶融粘度を測定したところ2×1
06 poise であった。上記トナーを図1に示す
定着装置を装着したミノルタ製複写機(EP−5400
)に投入し、OHPシート上に作像して定着後、透光性
、定着性、及び耐オフセット性の評価を行った。この結
果を表1に示す。表中、OHP透光性の評価で○はクリ
アな色で透光性が良好であったこと、×は黒ずんでいた
ことを示す。また、定着性の評価で○は折り曲げた部分
のみ白く欠損していたこと、×は折り曲げた周辺部まで
白く欠損していたことを示す。また、耐オフセット性の
評価で○はオフセットが発生しなかったこと、×はオフ
セットが発生したことを示す。The melt viscosity of this toner at 100° C. was measured using a descending flow tester melt viscosity measuring device, and the result was 2×1.
It was 06 poise. The above toner was transferred to a Minolta copier (EP-5400) equipped with the fixing device shown in Figure 1.
), and after forming an image on an OHP sheet and fixing it, the light transmittance, fixing property, and offset resistance were evaluated. The results are shown in Table 1. In the table, in the evaluation of OHP translucency, ◯ indicates that the color was clear and the translucency was good, and × indicates that it was darkened. Further, in the evaluation of fixability, ○ indicates that white defects were present only in the folded portion, and × indicates that white defects were observed in the folded portion. Further, in the evaluation of offset resistance, ◯ indicates that no offset occurred, and × indicates that offset occurred.
【0018】なお、上記定着装置は、ヒータ11を内蔵
する加熱ローラ1と加圧ローラ2とから構成されており
、両ローラは付勢バネ3により片方で30kg、両方で
60kgの圧力で圧着されている。加熱ローラ1はアル
ミニウム製芯金12(外径39.6mm、長さ318m
m)の表面を30μm厚さのPTFE系フッ素樹脂層1
3で被覆して形成されている。そして、加熱ローラ1の
表面粗さはRz2.5μmに研磨調整されている。また
、加熱ローラ1の表面には検温素子4及び分離爪5が設
置されている。一方、加圧ローラ2は鉄製芯金21(外
径30mm、長さ320mm)の表面を5mm厚さのシ
リコーンゴム層22で被覆して形成されている。この定
着装置における定着速度は110mm/secである。
(比較例1)上記実施例1の加熱ローラの表面粗さをR
z3.5μmとすること以外は実施例1と同一条件で上
記と同様の評価を行った。その結果を併せて表1に示す
。(比較例2)上記実施例1のスチレン−アクリル樹脂
のMn を2500(Mw /Mn ≒47)に変更し
たトナーを作成し、上記実施例1と同一条件で同様の評
価を行った。その結果を併せて表1に示す。なお、この
スチレン−アクリル樹脂の100℃での溶融粘度は1.
1×106poiseであった。(比較例3)上記実施
例1のスチレン−アクリル樹脂のMn を3500、M
w /Mn ≒40に変更したトナーを作成し、上記実
施例1と同一条件で同様の評価を行った。その結果を併
せて表1に示す。なお、このスチレン−アクリル樹脂の
100℃での溶融粘度は1.3×106 poise
であった。(比較例4)上記実施例1のスチレン−アク
リル樹脂のMn を4200,Mw /Mn ≒45に
変更したトナーを作成し、上記実施例1と同一条件で同
様の評価を行った。その結果を併せて表1に示す。
なお、このスチレン−アクリル樹脂の100℃での溶融
粘度は3.5×106 poise であった。The above-mentioned fixing device is composed of a heating roller 1 having a built-in heater 11 and a pressure roller 2, and both rollers are pressed together by a biasing spring 3 with a pressure of 30 kg on one side and 60 kg on both rollers. ing. The heating roller 1 is made of an aluminum core 12 (outer diameter 39.6 mm, length 318 m).
PTFE-based fluororesin layer 1 with a thickness of 30 μm on the surface of
It is coated with 3. The surface roughness of the heating roller 1 is polished to Rz 2.5 μm. Further, a temperature measuring element 4 and a separating claw 5 are installed on the surface of the heating roller 1. On the other hand, the pressure roller 2 is formed by covering the surface of an iron core metal 21 (outer diameter 30 mm, length 320 mm) with a silicone rubber layer 22 having a thickness of 5 mm. The fixing speed in this fixing device is 110 mm/sec. (Comparative Example 1) The surface roughness of the heating roller of Example 1 was set to R
The same evaluation as above was performed under the same conditions as in Example 1 except that z was set to 3.5 μm. The results are also shown in Table 1. (Comparative Example 2) A toner was prepared in which the Mn of the styrene-acrylic resin of Example 1 was changed to 2500 (Mw/Mn≈47), and the same evaluation as in Example 1 was performed under the same conditions. The results are also shown in Table 1. The melt viscosity of this styrene-acrylic resin at 100°C is 1.
It was 1×106 poise. (Comparative Example 3) Mn of the styrene-acrylic resin of Example 1 was 3500, M
A toner with w/Mn≈40 was prepared and evaluated in the same manner as in Example 1 above. The results are also shown in Table 1. The melt viscosity of this styrene-acrylic resin at 100°C is 1.3 x 106 poise
Met. (Comparative Example 4) A toner was prepared in which the Mn of the styrene-acrylic resin of Example 1 was changed to 4200 and Mw /Mn ≈45, and the same evaluation as in Example 1 was performed under the same conditions. The results are also shown in Table 1. The melt viscosity of this styrene-acrylic resin at 100°C was 3.5 x 106 poise.
【0019】[0019]
【表1】
本実施例1では、加熱ローラにオイルを塗布するこ
となしに、OHP透光性及び定着性が良好となり、また
オフセットが発生することもなかった。[Table 1] In Example 1, OHP translucency and fixing properties were good without applying oil to the heating roller, and no offset occurred.
【0020】一方、比較例1では、加熱ローラの表面粗
さがRz3.5μmと粗いため、OHPシート上に定着
されたトナー表面が不均一となり、光の反射等の影響に
よりOHP透光性が低下した。また、比較例2では、カ
ラートナーのバインダ成分としての樹脂の数平均分子量
が2500と小さい。このため、樹脂の凝集力が小さく
トナーとOHPシートとの定着性が低下し、また、トナ
ーと加熱ローラとの離型性が低下してオフセットが発生
した。On the other hand, in Comparative Example 1, since the surface roughness of the heating roller is as rough as Rz 3.5 μm, the surface of the toner fixed on the OHP sheet becomes uneven, and the OHP translucency deteriorates due to the influence of light reflection, etc. decreased. Further, in Comparative Example 2, the number average molecular weight of the resin as a binder component of the color toner is as small as 2,500. For this reason, the cohesive force of the resin was low, and the fixing ability between the toner and the OHP sheet was reduced, and the releasability between the toner and the heating roller was also reduced, causing offset.
【0021】また、比較例3では、カラートナーのバイ
ンダ成分としての樹脂の分子量分布が40と小さい。こ
のため凝集力が小さくなり、オフセットが発生した。さ
らに、比較例4では、カラートナーのバインダ成分とし
ての樹脂の数平均分子量が4200と大きく、また10
0℃での溶融粘度も3.5×106と大きい。このため
、トナーの溶融が不完全でフィルム状とならないため、
OHP透光性が低下した。Furthermore, in Comparative Example 3, the molecular weight distribution of the resin as a binder component of the color toner was as small as 40. As a result, the cohesive force decreased and offset occurred. Furthermore, in Comparative Example 4, the number average molecular weight of the resin as a binder component of the color toner was as large as 4200, and 10
The melt viscosity at 0°C is also as high as 3.5 x 106. For this reason, the toner is not completely melted and does not form a film.
OHP translucency decreased.
【0022】[0022]
【発明の効果】以上詳述したように、本発明のカラー複
写画像の定着方法は、耐久面で有利なフッ素樹脂系の熱
ローラ定着システムで、OHP透光性、定着性、及び耐
オフセット性を確保することが可能となった。したがっ
て、長期間にわたって信頼性の高い画像定着を行うこと
ができる。As described in detail above, the color copy image fixing method of the present invention uses a fluororesin-based hot roller fixing system that is advantageous in terms of durability, and has excellent OHP translucency, fixing performance, and offset resistance. It became possible to secure the Therefore, highly reliable image fixing can be performed for a long period of time.
【図1】実施例で使用した定着装置の側面図である。FIG. 1 is a side view of a fixing device used in an example.
【図2】スチレン−アクリル樹脂の100℃での溶融粘
度と数平均分子量との関係を示すグラフである。FIG. 2 is a graph showing the relationship between melt viscosity at 100° C. and number average molecular weight of styrene-acrylic resin.
1は加熱ローラ、2は加圧ローラ2、13はフッ素樹脂
層である。1 is a heating roller, 2 is a pressure roller 2, and 13 is a fluororesin layer.
Claims (1)
μm以下の表面粗さをもつ加熱ローラ、及び該加熱ロー
ラに圧接する加圧ローラ間にトナー画像を保持する記録
紙を該トナー画像面が該加熱ローラに面するように通過
させることにより該トナー画像を該記録紙上に定着させ
るカラー複写画像の定着方法において、100℃におけ
る溶融粘度が5×105 〜3×106 poise
、分子量分布(Mw /Mn 、Mw :重量平均分子
量、Mn :数平均分子量)が45以上、数平均分子量
(Mn )が1000〜4000である樹脂をバインダ
成分として含むカラートナーを使用することを特徴とす
るカラー複写画像の定着方法。[Claim 1] The surface is made of fluororesin and Rz3.0
By passing a recording paper holding a toner image between a heating roller having a surface roughness of μm or less and a pressure roller that is in pressure contact with the heating roller so that the toner image surface faces the heating roller, the toner can be removed. In a color copy image fixing method for fixing an image onto the recording paper, the melt viscosity at 100°C is 5 x 105 to 3 x 106 poise.
, a color toner containing a resin as a binder component having a molecular weight distribution (Mw/Mn, Mw: weight average molecular weight, Mn: number average molecular weight) of 45 or more and a number average molecular weight (Mn) of 1000 to 4000 is used. A method for fixing a color copy image.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP3007064A JPH04240660A (en) | 1991-01-24 | 1991-01-24 | Method for fixing color copied image |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP3007064A JPH04240660A (en) | 1991-01-24 | 1991-01-24 | Method for fixing color copied image |
Publications (1)
Publication Number | Publication Date |
---|---|
JPH04240660A true JPH04240660A (en) | 1992-08-27 |
Family
ID=11655640
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP3007064A Pending JPH04240660A (en) | 1991-01-24 | 1991-01-24 | Method for fixing color copied image |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH04240660A (en) |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0593052A1 (en) * | 1992-10-15 | 1994-04-20 | Canon Kabushiki Kaisha | Magnetic developer for developing electrostatic images |
WO2013058279A1 (en) | 2011-10-21 | 2013-04-25 | 日華化学株式会社 | Non-crystalline polyester resin, and binder resin and binder resin dispersion for toner |
JP2015090378A (en) * | 2013-11-05 | 2015-05-11 | シャープ株式会社 | Image forming apparatus and design method thereof |
-
1991
- 1991-01-24 JP JP3007064A patent/JPH04240660A/en active Pending
Cited By (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0593052A1 (en) * | 1992-10-15 | 1994-04-20 | Canon Kabushiki Kaisha | Magnetic developer for developing electrostatic images |
US5364720A (en) * | 1992-10-15 | 1994-11-15 | Canon Kabushiki Kaisha | Magnetic developer for developing electrostatic images |
WO2013058279A1 (en) | 2011-10-21 | 2013-04-25 | 日華化学株式会社 | Non-crystalline polyester resin, and binder resin and binder resin dispersion for toner |
US9234072B2 (en) | 2011-10-21 | 2016-01-12 | Nicca Chemical Co., Ltd. | Non-crystalline polyester resin, and binder resin and binder resin dispersion for toner |
JP2015090378A (en) * | 2013-11-05 | 2015-05-11 | シャープ株式会社 | Image forming apparatus and design method thereof |
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