JPH0934285A - Heat fixing method - Google Patents
Heat fixing methodInfo
- Publication number
- JPH0934285A JPH0934285A JP18688195A JP18688195A JPH0934285A JP H0934285 A JPH0934285 A JP H0934285A JP 18688195 A JP18688195 A JP 18688195A JP 18688195 A JP18688195 A JP 18688195A JP H0934285 A JPH0934285 A JP H0934285A
- Authority
- JP
- Japan
- Prior art keywords
- fixing
- recording material
- roller
- silicone oil
- fluorine
- 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 35
- 239000000463 material Substances 0.000 claims abstract description 65
- 229920002545 silicone oil Polymers 0.000 claims abstract description 42
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 claims abstract description 40
- 229910000019 calcium carbonate Inorganic materials 0.000 claims abstract description 20
- 239000011248 coating agent Substances 0.000 claims abstract description 12
- 238000000576 coating method Methods 0.000 claims abstract description 12
- 239000011164 primary particle Substances 0.000 claims abstract description 8
- 125000003709 fluoroalkyl group Chemical group 0.000 claims abstract description 4
- 125000003118 aryl group Chemical group 0.000 claims abstract description 3
- 125000001183 hydrocarbyl group Chemical group 0.000 claims abstract 2
- 229910052731 fluorine Inorganic materials 0.000 claims description 28
- YCKRFDGAMUMZLT-UHFFFAOYSA-N Fluorine atom Chemical compound [F] YCKRFDGAMUMZLT-UHFFFAOYSA-N 0.000 claims description 27
- 239000011737 fluorine Substances 0.000 claims description 27
- 238000010438 heat treatment Methods 0.000 claims description 19
- 125000004432 carbon atom Chemical group C* 0.000 claims description 5
- 238000002844 melting Methods 0.000 claims description 3
- 230000008018 melting Effects 0.000 claims description 3
- 238000003825 pressing Methods 0.000 claims description 2
- 229930195734 saturated hydrocarbon Natural products 0.000 claims description 2
- 229920001577 copolymer Polymers 0.000 abstract description 6
- JZZIHCLFHIXETF-UHFFFAOYSA-N dimethylsilicon Chemical compound C[Si]C JZZIHCLFHIXETF-UHFFFAOYSA-N 0.000 abstract description 2
- 230000015556 catabolic process Effects 0.000 abstract 1
- 238000006731 degradation reaction Methods 0.000 abstract 1
- LAQFLZHBVPULPL-UHFFFAOYSA-N methyl(phenyl)silicon Chemical compound C[Si]C1=CC=CC=C1 LAQFLZHBVPULPL-UHFFFAOYSA-N 0.000 abstract 1
- 239000002245 particle Substances 0.000 description 13
- 230000000694 effects Effects 0.000 description 9
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 6
- 150000001875 compounds Chemical class 0.000 description 6
- 125000000217 alkyl group Chemical group 0.000 description 5
- 239000011347 resin Substances 0.000 description 5
- 229920005989 resin Polymers 0.000 description 5
- 238000012546 transfer Methods 0.000 description 5
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 4
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 4
- -1 alkenyl succinic anhydride Chemical compound 0.000 description 4
- 150000001349 alkyl fluorides Chemical class 0.000 description 4
- 239000003795 chemical substances by application Substances 0.000 description 4
- 125000000118 dimethyl group Chemical group [H]C([H])([H])* 0.000 description 4
- 238000011156 evaluation Methods 0.000 description 4
- 238000004519 manufacturing process Methods 0.000 description 4
- 239000005995 Aluminium silicate Substances 0.000 description 3
- 239000000654 additive Substances 0.000 description 3
- 150000001348 alkyl chlorides Chemical class 0.000 description 3
- 235000012211 aluminium silicate Nutrition 0.000 description 3
- 238000010586 diagram Methods 0.000 description 3
- 239000010419 fine particle Substances 0.000 description 3
- 229910052742 iron Inorganic materials 0.000 description 3
- NLYAJNPCOHFWQQ-UHFFFAOYSA-N kaolin Chemical compound O.O.O=[Al]O[Si](=O)O[Si](=O)O[Al]=O NLYAJNPCOHFWQQ-UHFFFAOYSA-N 0.000 description 3
- 239000006249 magnetic particle Substances 0.000 description 3
- 238000005259 measurement Methods 0.000 description 3
- 230000007246 mechanism Effects 0.000 description 3
- 108091008695 photoreceptors Proteins 0.000 description 3
- 229920002379 silicone rubber Polymers 0.000 description 3
- 239000000454 talc Substances 0.000 description 3
- 229910052623 talc Inorganic materials 0.000 description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 3
- 238000004804 winding Methods 0.000 description 3
- 229910000859 α-Fe Inorganic materials 0.000 description 3
- 239000004925 Acrylic resin Substances 0.000 description 2
- 229920000178 Acrylic resin Polymers 0.000 description 2
- ODINCKMPIJJUCX-UHFFFAOYSA-N Calcium oxide Chemical compound [Ca]=O ODINCKMPIJJUCX-UHFFFAOYSA-N 0.000 description 2
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 2
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 description 2
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 2
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 2
- 239000006229 carbon black Substances 0.000 description 2
- 230000008859 change Effects 0.000 description 2
- 238000004140 cleaning Methods 0.000 description 2
- 230000000052 comparative effect Effects 0.000 description 2
- 235000014113 dietary fatty acids Nutrition 0.000 description 2
- 239000000194 fatty acid Substances 0.000 description 2
- 229930195729 fatty acid Natural products 0.000 description 2
- 150000004665 fatty acids Chemical class 0.000 description 2
- 239000000945 filler Substances 0.000 description 2
- 125000001153 fluoro group Chemical group F* 0.000 description 2
- 239000011121 hardwood Substances 0.000 description 2
- 230000002209 hydrophobic effect Effects 0.000 description 2
- 238000005470 impregnation Methods 0.000 description 2
- 239000000696 magnetic material Substances 0.000 description 2
- 229910052751 metal Inorganic materials 0.000 description 2
- 239000002184 metal Substances 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- 230000004048 modification Effects 0.000 description 2
- 238000012986 modification Methods 0.000 description 2
- 230000007935 neutral effect Effects 0.000 description 2
- 239000003921 oil Substances 0.000 description 2
- 238000005498 polishing Methods 0.000 description 2
- 229920001225 polyester resin Polymers 0.000 description 2
- 239000004645 polyester resin Substances 0.000 description 2
- 229920001721 polyimide Polymers 0.000 description 2
- 238000007639 printing Methods 0.000 description 2
- 229910052710 silicon Inorganic materials 0.000 description 2
- 239000000377 silicon dioxide Substances 0.000 description 2
- LAIRCTXAVVHREG-UHFFFAOYSA-N 1-chlorobutane 1-chloropropane Chemical compound C(CCC)Cl.ClCCC LAIRCTXAVVHREG-UHFFFAOYSA-N 0.000 description 1
- IICCLYANAQEHCI-UHFFFAOYSA-N 4,5,6,7-tetrachloro-3',6'-dihydroxy-2',4',5',7'-tetraiodospiro[2-benzofuran-3,9'-xanthene]-1-one Chemical compound O1C(=O)C(C(=C(Cl)C(Cl)=C2Cl)Cl)=C2C21C1=CC(I)=C(O)C(I)=C1OC1=C(I)C(O)=C(I)C=C21 IICCLYANAQEHCI-UHFFFAOYSA-N 0.000 description 1
- 235000019738 Limestone Nutrition 0.000 description 1
- AZTTYKSNKVFVIW-UHFFFAOYSA-N N=C=O.C1NC1 Chemical class N=C=O.C1NC1 AZTTYKSNKVFVIW-UHFFFAOYSA-N 0.000 description 1
- 239000004697 Polyetherimide Substances 0.000 description 1
- 239000004642 Polyimide Substances 0.000 description 1
- 239000004743 Polypropylene Substances 0.000 description 1
- 229920001131 Pulp (paper) Polymers 0.000 description 1
- 239000006087 Silane Coupling Agent Substances 0.000 description 1
- 239000004809 Teflon Substances 0.000 description 1
- 229920006362 Teflon® Polymers 0.000 description 1
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 description 1
- QYKIQEUNHZKYBP-UHFFFAOYSA-N Vinyl ether Chemical compound C=COC=C QYKIQEUNHZKYBP-UHFFFAOYSA-N 0.000 description 1
- 230000002378 acidificating effect Effects 0.000 description 1
- 230000000996 additive effect Effects 0.000 description 1
- 229910052782 aluminium Inorganic materials 0.000 description 1
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-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
- CCDWGDHTPAJHOA-UHFFFAOYSA-N benzylsilicon Chemical compound [Si]CC1=CC=CC=C1 CCDWGDHTPAJHOA-UHFFFAOYSA-N 0.000 description 1
- 239000011230 binding agent Substances 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 239000000292 calcium oxide Substances 0.000 description 1
- 235000012255 calcium oxide Nutrition 0.000 description 1
- 239000001569 carbon dioxide Substances 0.000 description 1
- 229910002092 carbon dioxide Inorganic materials 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 125000001309 chloro group Chemical group Cl* 0.000 description 1
- NEHMKBQYUWJMIP-NJFSPNSNSA-N chloro(114C)methane Chemical compound [14CH3]Cl NEHMKBQYUWJMIP-NJFSPNSNSA-N 0.000 description 1
- HRYZWHHZPQKTII-UHFFFAOYSA-N chloroethane Chemical compound CCCl HRYZWHHZPQKTII-UHFFFAOYSA-N 0.000 description 1
- 239000003086 colorant Substances 0.000 description 1
- 239000004020 conductor Substances 0.000 description 1
- 238000010276 construction Methods 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
- 239000007822 coupling agent Substances 0.000 description 1
- 238000002425 crystallisation Methods 0.000 description 1
- 230000008025 crystallization Effects 0.000 description 1
- 125000004122 cyclic group Chemical group 0.000 description 1
- 230000007547 defect Effects 0.000 description 1
- 239000002761 deinking Substances 0.000 description 1
- MROCJMGDEKINLD-UHFFFAOYSA-N dichlorosilane Chemical class Cl[SiH2]Cl MROCJMGDEKINLD-UHFFFAOYSA-N 0.000 description 1
- 239000004205 dimethyl polysiloxane Substances 0.000 description 1
- 235000013870 dimethyl polysiloxane Nutrition 0.000 description 1
- BPYFPNZHLXDIGA-UHFFFAOYSA-N diphenylsilicon Chemical compound C=1C=CC=CC=1[Si]C1=CC=CC=C1 BPYFPNZHLXDIGA-UHFFFAOYSA-N 0.000 description 1
- KPUWHANPEXNPJT-UHFFFAOYSA-N disiloxane Chemical class [SiH3]O[SiH3] KPUWHANPEXNPJT-UHFFFAOYSA-N 0.000 description 1
- 229920001971 elastomer Polymers 0.000 description 1
- 230000007613 environmental effect Effects 0.000 description 1
- RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Substances CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 1
- 229960003750 ethyl chloride Drugs 0.000 description 1
- 239000004744 fabric Substances 0.000 description 1
- 150000002222 fluorine compounds Chemical class 0.000 description 1
- 238000009472 formulation Methods 0.000 description 1
- 230000004927 fusion Effects 0.000 description 1
- 150000002430 hydrocarbons Chemical group 0.000 description 1
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 1
- 230000007062 hydrolysis Effects 0.000 description 1
- 238000006460 hydrolysis reaction Methods 0.000 description 1
- 229910052809 inorganic oxide Inorganic materials 0.000 description 1
- 230000003993 interaction Effects 0.000 description 1
- SZVJSHCCFOBDDC-UHFFFAOYSA-N iron(II,III) oxide Inorganic materials O=[Fe]O[Fe]O[Fe]=O SZVJSHCCFOBDDC-UHFFFAOYSA-N 0.000 description 1
- 230000001788 irregular Effects 0.000 description 1
- MOUPNEIJQCETIW-UHFFFAOYSA-N lead chromate Chemical compound [Pb+2].[O-][Cr]([O-])(=O)=O MOUPNEIJQCETIW-UHFFFAOYSA-N 0.000 description 1
- 239000006028 limestone Substances 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 229940002712 malachite green oxalate Drugs 0.000 description 1
- CXKWCBBOMKCUKX-UHFFFAOYSA-M methylene blue Chemical compound [Cl-].C1=CC(N(C)C)=CC2=[S+]C3=CC(N(C)C)=CC=C3N=C21 CXKWCBBOMKCUKX-UHFFFAOYSA-M 0.000 description 1
- 125000000325 methylidene group Chemical group [H]C([H])=* 0.000 description 1
- 239000010893 paper waste Substances 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- 229920000435 poly(dimethylsiloxane) Polymers 0.000 description 1
- 229920000728 polyester Polymers 0.000 description 1
- 229920001601 polyetherimide Polymers 0.000 description 1
- 238000006116 polymerization reaction Methods 0.000 description 1
- 229920000098 polyolefin Polymers 0.000 description 1
- 229920001155 polypropylene Polymers 0.000 description 1
- 229920001343 polytetrafluoroethylene Polymers 0.000 description 1
- 239000004810 polytetrafluoroethylene Substances 0.000 description 1
- 239000004172 quinoline yellow Substances 0.000 description 1
- 229940051201 quinoline yellow Drugs 0.000 description 1
- 235000012752 quinoline yellow Nutrition 0.000 description 1
- IZMJMCDDWKSTTK-UHFFFAOYSA-N quinoline yellow Chemical compound C1=CC=CC2=NC(C3C(C4=CC=CC=C4C3=O)=O)=CC=C21 IZMJMCDDWKSTTK-UHFFFAOYSA-N 0.000 description 1
- 229940081623 rose bengal Drugs 0.000 description 1
- 229930187593 rose bengal Natural products 0.000 description 1
- STRXNPAVPKGJQR-UHFFFAOYSA-N rose bengal A Natural products O1C(=O)C(C(=CC=C2Cl)Cl)=C2C21C1=CC(I)=C(O)C(I)=C1OC1=C(I)C(O)=C(I)C=C21 STRXNPAVPKGJQR-UHFFFAOYSA-N 0.000 description 1
- 229940058287 salicylic acid derivative anticestodals Drugs 0.000 description 1
- 150000003872 salicylic acid derivatives Chemical class 0.000 description 1
- 239000010703 silicon Substances 0.000 description 1
- 239000004945 silicone rubber Substances 0.000 description 1
- 238000004513 sizing Methods 0.000 description 1
- 239000011122 softwood Substances 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 229920005792 styrene-acrylic resin Polymers 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 239000000758 substrate Substances 0.000 description 1
- 229940014800 succinic anhydride Drugs 0.000 description 1
- BFKJFAAPBSQJPD-UHFFFAOYSA-N tetrafluoroethene Chemical group FC(F)=C(F)F BFKJFAAPBSQJPD-UHFFFAOYSA-N 0.000 description 1
- 239000010936 titanium Substances 0.000 description 1
- 229910052719 titanium Inorganic materials 0.000 description 1
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 description 1
- 235000013799 ultramarine blue Nutrition 0.000 description 1
- 230000000007 visual effect Effects 0.000 description 1
- XOSXWYQMOYSSKB-LDKJGXKFSA-L water blue Chemical compound CC1=CC(/C(\C(C=C2)=CC=C2NC(C=C2)=CC=C2S([O-])(=O)=O)=C(\C=C2)/C=C/C\2=N\C(C=C2)=CC=C2S([O-])(=O)=O)=CC(S(O)(=O)=O)=C1N.[Na+].[Na+] XOSXWYQMOYSSKB-LDKJGXKFSA-L 0.000 description 1
- 239000001993 wax Substances 0.000 description 1
- 230000037303 wrinkles Effects 0.000 description 1
Landscapes
- Fixing For Electrophotography (AREA)
Abstract
Description
【0001】[0001]
【産業上の利用分野】本発明は熱定着方法に関し、特に
紙との接着性が良好で定着効率の良い熱定着方法に関す
るものである。BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a heat fixing method, and more particularly to a heat fixing method having good adhesion to paper and good fixing efficiency.
【0002】[0002]
【従来の技術】従来、電子写真法においては、記録材上
に担持されたトナー像の熱効率が良く、高速定着に適す
る等の理由から熱ローラ定着方法が賞用されてきた。こ
の熱ローラ定着方法は、加熱源を内蔵した定着ローラー
と圧着ローラーとの間をトナー像を担持した記録紙を通
過させ、トナーを記録紙へ熱溶融定着させる方法であ
る。2. Description of the Related Art Conventionally, in electrophotography, a heat roller fixing method has been favored because it has a high thermal efficiency of a toner image carried on a recording material and is suitable for high speed fixing. This heat roller fixing method is a method in which a recording paper carrying a toner image is passed between a fixing roller having a built-in heat source and a pressure roller to heat and fix the toner on the recording paper.
【0003】この熱ローラ定着方法は、上記長所を有す
る反面、負帯電性の高い転写紙を用いた場合には静電的
な反発があり、ローラーに対する密着性は低くくなりこ
の結果、紙に対する熱の伝達が不足し熱定着率が悪くな
る。This heat roller fixing method has the above-mentioned advantages, but on the other hand, when a transfer paper having a high negative charging property is used, there is electrostatic repulsion, and the adhesion to the roller becomes low. The heat transfer is insufficient and the heat fixing rate becomes poor.
【0004】又、熱ローラ定着方法のオフセット現象発
生防止のため、従来定着ローラ表面にジメチルシリコン
オイルを供給する技術が提案されているが、ジメチルシ
リコンオイルは正帯電性を有し、中性紙に填料として用
いられる炭酸カルシウムは正帯電性を有するものである
為、中性紙が反発しやすくなり、この結果、紙の定着装
置に対する密着性が低下するため、定着効率が低下する
傾向にある。In order to prevent the occurrence of the offset phenomenon in the heat roller fixing method, a technique of supplying dimethyl silicone oil to the surface of the fixing roller has been proposed in the past. However, dimethyl silicone oil has a positive charging property and is a neutral paper. Since calcium carbonate used as a filler in the toner has a positive charging property, the neutral paper is likely to repel, and as a result, the adhesiveness of the paper to the fixing device is reduced, so that the fixing efficiency tends to be reduced. .
【0005】近年、定着ローラに対する濡れ性が良好で
均一な塗布が可能であることから、含フッ素系シリコン
オイルを用いる熱定着方法が提案されているが、該含フ
ッ素系シリコンオイルは負帯電性が強く、酸性紙に填料
として一般的に使用されるカオリン、タルク等は負帯電
性を有するものであり、この結果、これらを用いた紙は
負帯電性を有するものとなる為、該含フッ素系シリコン
オイルを用いた定着装置に対する静電気的な反発で紙の
定着装置に対する密着性が低下し、この場合も定着性の
低下を招いてしまうという問題を有している。又、紙の
定着装置に対する密着性を良くすると定着ローラー及び
フィルム傷の発生が起こることも分かった。In recent years, a thermal fixing method using a fluorine-containing silicone oil has been proposed because it has good wettability to a fixing roller and uniform coating is possible. However, the fluorine-containing silicone oil has a negative charging property. Since kaolin, talc, etc., which are generally used as a filler in acidic papers, have a negative charge property, and as a result, the papers using these have a negative charge property, the fluorine-containing There is a problem in that the adhesion of paper to the fixing device is reduced due to electrostatic repulsion to the fixing device using the system silicone oil, and in this case also the fixing property is reduced. It has also been found that when the adhesion of the paper to the fixing device is improved, the fixing roller and the film are damaged.
【0006】[0006]
【発明が解決しようとする課題】本発明の目的は、上記
問題を鑑み、含フッ素系シリコンオイルを用いた熱定着
方法において、定着部での静電的な反発による、紙の定
着装置に対する密着性の低下が無く、定着効率に優れ、
且つ定着ローラー及びフィルム傷の発生の無い熱定着方
法を提供することにある。SUMMARY OF THE INVENTION In view of the above problems, an object of the present invention is to provide a thermal fixing method using a fluorine-containing silicone oil, and to adhere the paper to the fixing device by electrostatic repulsion at the fixing section. With excellent fixing efficiency
Another object of the present invention is to provide a fixing roller and a thermal fixing method that does not cause film scratches.
【0007】[0007]
【課題を解決するための手段】本発明の上記目的は、以
下の構成により達成される。The above object of the present invention is achieved by the following constitution.
【0008】1.移動する定着部材、該定着部材に移動
する記録材を圧接する圧着部材及び該定着部材を介し
て、該記録材上のトナー像を熱熔融する加熱手段を設け
てなる熱定着方法において、前記定着部材の記録材と接
触する側の表面に、下記一般式〔I〕で示される構造単
位を有する含フッ素系シリコンオイル塗膜を形成し、且
つ記録材が数平均一次粒子径0.1〜3.0μmの炭酸
カルシウムを含有することを特徴とする熱定着方法。[0008] 1. In the thermal fixing method, a moving fixing member, a pressure-bonding member for pressing a moving recording material to the fixing member, and a heating unit for melting the toner image on the recording material through the fixing member are provided. A fluorine-containing silicone oil coating film having a structural unit represented by the following general formula [I] is formed on the surface of the member that contacts the recording material, and the recording material has a number average primary particle diameter of 0.1 to 3 A heat fixing method characterized by containing calcium carbonate of 0.0 μm.
【0009】[0009]
【化2】 Embedded image
【0010】式中、Xは炭素数1〜4の飽和炭化水素基
又はアリール基を示し、Rfは炭素原子数2〜10のフ
ルオロアルキル基を示し、nは1〜4の整数を示す。In the formula, X represents a saturated hydrocarbon group having 1 to 4 carbon atoms or an aryl group, R f represents a fluoroalkyl group having 2 to 10 carbon atoms, and n represents an integer of 1 to 4.
【0011】2.前記定着部材が、前記加熱手段を内蔵
した定着ローラーであることを特徴とする前記1記載の
熱定着方法。2. 2. The heat fixing method according to the above 1, wherein the fixing member is a fixing roller having the heating unit built therein.
【0012】この構成では紙自体の帯電性を正帯電化す
ることにより、特に特定構造を有する含フッ素系シリコ
ンオイルを用いた定着装置に対する密着性を向上するこ
とができ、定着率を上げることができるものと推定して
いる。In this construction, by positively charging the chargeability of the paper itself, it is possible to improve the adhesion to a fixing device using a fluorine-containing silicone oil having a specific structure, thereby increasing the fixing rate. It is estimated to be possible.
【0013】以下、本発明を詳細に述べる。The present invention will be described in detail below.
【0014】本発明のシリコンオイルは前記一般式
〔I〕で示される構造の繰り返し単位を有していること
が必須であるが、ジメチルシリコン、フェニルメチルシ
リコン、ジフェニルシリコン等と共重合体構造を有して
いてもよい。本発明の含フッ素系シリコンオイルは使用
時において適度な粘度を有する液状のものであることが
好ましい。このため、本発明の含フッ素系シリコンオイ
ルは25℃における粘度が20〜l000CSが好まし
く、更に好ましくはl00〜500CSの粘度を有するも
のがよい。Although it is essential that the silicone oil of the present invention has a repeating unit having the structure represented by the above general formula [I], it has a copolymer structure with dimethylsilicon, phenylmethylsilicon, diphenylsilicon or the like. You may have. The fluorinated silicone oil of the present invention is preferably a liquid having an appropriate viscosity when used. Therefore, fluorine-containing silicone oil of the present invention is preferably viscosity 20~L000 CS at 25 ° C., more preferably be those having a viscosity of l00~500 CS.
【0015】この粘度の調整は重合度を調整することで
制御することができる。この粘度は動的粘度を示し、A
STMD445−46T、或いはJ1SZ8808に準
拠し、ウッベローデ粘度計により測定されるものであ
る。The adjustment of the viscosity can be controlled by adjusting the degree of polymerization. This viscosity indicates the dynamic viscosity, A
According to STMD445-46T or J1SZ8808, it is measured by an Ubbelohde viscometer.
【0016】本発明の含フッ素系シリコンオイルが共重
合体である場合、本発明の諸目的達成度から、本発明の
一般式〔I〕で示される構造単位が20〜99.9%含
まれていればよい。20%未満であると本発明の含フッ
素系シリコンオイルの効果が発揮されず、他の成分の影
響、即ち本発明の含フッ素系シリコンオイルの効果が低
下してしまう。When the fluorine-containing silicone oil of the present invention is a copolymer, the structural unit represented by the general formula [I] of the present invention is contained in an amount of 20 to 99.9% in view of the achievement of various objects of the present invention. If you have. If it is less than 20%, the effect of the fluorinated silicone oil of the present invention will not be exhibited, and the effect of other components, that is, the effect of the fluorinated silicone oil of the present invention will decrease.
【0017】本発明の含フッ素系シリコンオイルの製造
方法は、通常のシリコンオイルの製造方法と同様にジア
ルキル置換ジクロロシランを珪素と塩化アルキルとの反
応で調製し、これを用いて加水分解することでシロキサ
ンとなし、ついで環状オリゴマー或いは線状オリゴマー
を形成した後にこれらを重合することで合成される。In the method for producing a fluorine-containing silicone oil of the present invention, a dialkyl-substituted dichlorosilane is prepared by the reaction of silicon with an alkyl chloride, and hydrolysis is carried out using the same, as in the ordinary silicone oil production method. To form a siloxane, and then to form a cyclic oligomer or a linear oligomer, and then polymerize these to synthesize.
【0018】本発明の含フッ素系シリコンオイル化合物
は側鎖にフッ化アルキル基を有しているものであるが、
この場合には塩化アルキルの代わりに末端にクロロ基を
有するフッ素系化合物、例えば下記一般式で示す構造の
ものを用いることで容易に製造される。Although the fluorine-containing silicone oil compound of the present invention has a fluorinated alkyl group in its side chain,
In this case, it can be easily produced by using a fluorine compound having a chloro group at the terminal, for example, one having a structure represented by the following general formula, instead of alkyl chloride.
【0019】Z−(CF2)m(CH2)nCl ここで、mは2〜10の整数を示し、nは1〜4の整数
を示す。また、Zは水素原子又はフッ素原子を示す。Z- (CF 2 ) m (CH 2 ) nCl Here, m represents an integer of 2 to 10 and n represents an integer of 1 to 4. Z represents a hydrogen atom or a fluorine atom.
【0020】具体的には下記に示す構造の化合物があげ
られる。Specific examples include compounds having the structures shown below.
【0021】(A)CF3CF2CH2Cl (B)CF3CF2CF2CH2Cl (C)CF3CF2CF2(CH2)2Cl (D)CF3CF2CF2CF2(CH2)2Cl (E)CF3CF2CF2CF2CF2CH2Cl (F)CF3CF2CF2CF2CF2(CH2)3Cl (G)CF3CF2CF2CF2CF2CF2CH2Cl (H)CF3CF2CF2CF2CF2CF2CF2CH2Cl (l)HCF2CF2CH2Cl (J)HCF2CF2CF2CH2Cl (K)HCF2CF2CF2(CH2)2Cl (L)HCF2CF2CF2CF2CH2Cl (M)HCF2CF2CF2CF2(CH2)2Cl (N)HCF2CF2CF2CF2(CH2)4Cl (O)HCF2CF2CF2CF2CF2(CH2)3cl (P)HCF2CF2CF2CF2CF2CF2CH2Cl なお、本発明においてフッ化アルキル基以外のアルキル
基を導入する塩化アルキルとしては塩化メチル、塩化エ
チル、塩化プロピル、塩化ブチルをあげることができ
る。(A) CF 3 CF 2 CH 2 Cl (B) CF 3 CF 2 CF 2 CH 2 Cl (C) CF 3 CF 2 CF 2 (CH 2 ) 2 Cl (D) CF 3 CF 2 CF 2 CF 2 (CH 2) 2 Cl ( E) CF 3 CF 2 CF 2 CF 2 CF 2 CH 2 Cl (F) CF 3 CF 2 CF 2 CF 2 CF 2 (CH 2) 3 Cl (G) CF 3 CF 2 CF 2 CF 2 CF 2 CF 2 CH 2 Cl (H) CF 3 CF 2 CF 2 CF 2 CF 2 CF 2 CF 2 CH 2 Cl (l) HCF 2 CF 2 CH 2 Cl (J) HCF 2 CF 2 CF 2 CH 2 Cl (K) HCF 2 CF 2 CF 2 (CH 2) 2 Cl (L) HCF 2 CF 2 CF 2 CF 2 CH 2 Cl (M) HCF 2 CF 2 CF 2 CF 2 (CH 2) 2 Cl (N ) HCF 2 CF 2 CF 2 CF 2 (CH 2) 4 Cl (O) HCF 2 CF 2 CF 2 CF 2 CF 2 (C 2) 3 cl (P) HCF 2 CF 2 CF 2 CF 2 CF 2 CF 2 CH 2 Cl As the alkyl chloride to introduce an alkyl group other than fluorinated alkyl group in the present invention include methyl chloride, ethyl chloride, propyl chloride Butyl chloride can be mentioned.
【0022】本発明においてはこのフッ化アルキル置換
されたシリコンオイルを用いることで、フッ素系樹脂を
被覆された定着ロールに均一に付着させ本発明の効果を
発揮させるためには、フッ化アルキルで置換されたシリ
コンオイルのフッ素原子の数が大きく寄与する。従って
フッ化アルキルの炭素数は1〜10であり、珪素原子に
直接結合する部分はメチレン鎖である。更に、フッ化ア
ルキルの好ましい範囲は2〜8である。このフッ化アル
キル炭素数が過多となると熱が加わった場合の流動特性
に問題を生じる。また、フッ化アルキルを有しない場合
にはフッ素系樹脂を被覆した熱ロール表面に対する濡れ
性の向上が無く、均一なオイル膜の形成ができない。In the present invention, in order to exert the effect of the present invention by uniformly attaching the fluororesin to the fixing roll coated by using the silicone oil substituted with the fluoroalkyl, the alkyl fluoride is used. The number of fluorine atoms in the substituted silicone oil contributes greatly. Therefore, the alkyl fluoride has 1 to 10 carbon atoms, and the portion directly bonded to the silicon atom is a methylene chain. Furthermore, the preferable range of alkyl fluoride is 2-8. If the number of fluorinated alkyl carbons is excessive, there will be a problem in the flow characteristics when heat is applied. Further, when the fluorinated alkyl is not contained, the wettability with respect to the surface of the heat roll coated with the fluororesin is not improved, and a uniform oil film cannot be formed.
【0023】本発明の一般式〔I〕で示される含フッ素
系シリコンオイルの構造を下記に示す。The structure of the fluorine-containing silicone oil represented by the general formula [I] of the present invention is shown below.
【0024】[0024]
【化3】 Embedded image
【0025】[0025]
【化4】 Embedded image
【0026】なお、ここで、a及びbは1以上の整数を
示し、好ましくは10〜2000の整数であり、更に好
ましくは100〜1000である。Here, a and b represent integers of 1 or more, preferably 10 to 2000, and more preferably 100 to 1000.
【0027】1.熱定着方法 本発明の熱定着方法は熱ローラ定着方法と移動するフィ
ルム材を加熱して行う方法に大別される。1. Heat Fixing Method The heat fixing method of the present invention is roughly classified into a heat roller fixing method and a method of heating a moving film material.
【0028】以下本発明に好適に適用される熱定着方法
について説明する。The heat fixing method preferably applied to the present invention will be described below.
【0029】本発明の熱ローラー定着方法を図1に従っ
て説明すると、表面2に例えばテトラフルオロエチレン
やポリテトラフルオロエチレン−パーフルオロアルキル
ビニルエーテル共重合体類等を被覆した鉄やアルミニウ
ム等で構成される金属シリンダ3内部に加熱源4を有す
る上ローラー1とシリコンゴム等で形成された下ローラ
ー5とから形成されているものである。詳しくは、加熱
源4として線状のヒーターを有し、上ローラー1の表面
温度を約110〜220℃程度に加熱させるものであ
る。この上ローラー1と下ローラー5との間を本発明の
トナー画像7を担持した記録材6を通過させ、トナー画
像7を記録材上に熱溶融固着させる。従来の熱ローラー
定着方法では、溶融したトナーの一部が上ローラー1に
融着し、一回転後、この上ローラー1に融着したトナー
が記録材の別の部分に固着されるオフセット現象が発生
し、甚だしき場合は、上ローラー1に融着したトナー
は、記録材から離れず記録材と共に上ローラー1に巻き
付く、所謂巻き付き現象が発生すると共に定着ローラー
表面が汚れるという問題を提起していた。定着部に於い
ては上ローラー1と下ローラー5間に圧力を加え、下ロ
ーラー5を変形させ、いわゆるニップを形成する。ニッ
プ幅としては1〜10mm、好ましくは1.5〜7mm
である。定着線速度は40〜400mm/secが好ま
しい。ニップ幅が狭い場合には熱を均一にトナーに付与
することができなくなり、定着のムラを発生し易くな
る。一方でニップ幅が広い場合にはトナーの溶融が促進
され、オフセット現象が発生しやすくなる。The hot roller fixing method of the present invention will be described with reference to FIG. 1. The surface 2 is made of iron, aluminum or the like coated with, for example, tetrafluoroethylene or polytetrafluoroethylene-perfluoroalkyl vinyl ether copolymers. It is formed of an upper roller 1 having a heating source 4 inside a metal cylinder 3 and a lower roller 5 made of silicon rubber or the like. Specifically, a linear heater is provided as the heating source 4, and the surface temperature of the upper roller 1 is heated to about 110 to 220 ° C. The recording material 6 carrying the toner image 7 of the present invention is passed between the upper roller 1 and the lower roller 5 to fix the toner image 7 on the recording material by heat fusion. In the conventional heat roller fixing method, a part of the melted toner is fused to the upper roller 1, and after one rotation, the toner fused to the upper roller 1 is fixed to another portion of the recording material. If the toner is generated and is extremely heavy, the toner fused to the upper roller 1 is not separated from the recording material and is wound around the upper roller 1 together with the recording material. This causes a so-called wrapping phenomenon and stains the surface of the fixing roller. It was In the fixing section, pressure is applied between the upper roller 1 and the lower roller 5 to deform the lower roller 5 and form a so-called nip. The nip width is 1 to 10 mm, preferably 1.5 to 7 mm
It is. The fixing linear velocity is preferably 40 to 400 mm / sec. If the nip width is narrow, heat cannot be uniformly applied to the toner, and uneven fixing tends to occur. On the other hand, when the nip width is wide, toner melting is promoted, and the offset phenomenon is likely to occur.
【0030】本発明の熱ローラー定着方法においては、
上ローラー1の表面2上には本発明の含フッ素系シリコ
ンオイル塗膜が形成されており、この塗膜と本発明の記
録材との相互作用によって、本発明の諸目的は効率的に
達成される。この本発明の含フッ素系シリコンオイル塗
膜の上ローラー1の表面2での形成は、一例として以下
の通りに行われる。In the heat roller fixing method of the present invention,
A fluorine-containing silicone oil coating film of the present invention is formed on the surface 2 of the upper roller 1, and the various objects of the present invention are efficiently achieved by the interaction between the coating film and the recording material of the present invention. To be done. The formation of the fluorine-containing silicone oil coating film of the present invention on the surface 2 of the upper roller 1 is performed as follows, for example.
【0031】即ち、上ローラー1の長手方向の表面2に
は、含浸ローラー8が圧接され、矢印方向に回転してい
る。この含浸ローラー8には、予め本発明の含フッ素系
シリコンオイルを含浸させておき、定着に際して、上ロ
ーラー1の回転に従って極少量ずつ含浸ローラー8から
上ローラー1の表面に含フッ素系シリコンオイルが供給
されて、結果として上ローラー1の表面2上には、本発
明の含フッ素系シリコンオイル塗膜が形成されることに
なる。That is, the impregnating roller 8 is pressed against the longitudinal surface 2 of the upper roller 1 and rotates in the direction of the arrow. The impregnating roller 8 is impregnated with the fluorine-containing silicone oil of the present invention in advance, and at the time of fixing, the impregnating roller 8 is coated with a small amount of fluorine-containing silicone oil on the surface of the upper roller 1 as the upper roller 1 rotates. As a result, the fluorine-containing silicone oil coating film of the present invention is formed on the surface 2 of the upper roller 1.
【0032】又、後者の定着方法は、図2に従って説明
すると装置に固定支持された低熱容量ライン状加熱体1
5は、厚さ0.2〜5.0mm、好ましくは0.5〜
3.5mm、幅10〜15mm、長手方向の長さ240
〜400mmのアルミナ基板17に抵抗材料を1.0〜
2.5mmに塗布したもので両端より通電されるもので
ある。通電はDC100Vの周期25msecのパルス
波形で温度センサ16により制御された温度を、エネル
ギー放出量に応じたパルス幅に変化させて与える。低熱
容量ライン状加熱体15において温度センサ16で検出
された温度T1の場合、抵抗材料に対向するフィルム材
14の表面温度T2は温度T1よりも低い温度となる。
ここで温度T1は110〜220℃が好ましく、T2の
温度はT1の温度と比較して0.5〜10℃低いことが
好ましい。また、フィルム材14がトナー定着表面より
剥離する部分におけるフィルム材表面温度T3はT2と
ほぼ同等である。この様にエネルギー制御、温度制御さ
れた加熱体に当接してフィルム材は記録材と同じ方向に
移動する。このフィルム材14としては、厚みにして1
0〜35μmの耐熱フィルム、例えば、ポリエステル、
ポリパーフルオロアルキルビニルエーテル、ポリイミ
ド、ポリエーテルイミドに少なくともテフロン等のフッ
素樹脂に導電材を添加した離型材層を5〜15μm被覆
させたフィルムであることが好ましく、更に好ましくは
エンドレスフィルム材である。一般的には総厚10〜1
00μm、フィルム材14の駆動はフィルム材駆動ロー
ラー11とフィルム材従動ローラー12による駆動とテ
ンションによりシワ、ヨレがなく搬送される。加圧ロー
ラー13はシリコンゴム等の離型性の高いゴム弾性層を
有し、総圧2〜30kgでフィルム材14を介して低熱
容量ライン状加熱体15と加圧し、矢印方向に圧接回転
し、このフィルム材14と加圧ローラー13との間をト
ナー像を担持した記録材を通過させることによって、低
熱容量ライン状加熱体15を通過させて、トナー像を記
録材に溶融固着させる。The latter fixing method will be described with reference to FIG. 2. The low heat capacity linear heating element 1 fixedly supported by the apparatus.
5 has a thickness of 0.2 to 5.0 mm, preferably 0.5 to
3.5 mm, width 10-15 mm, longitudinal length 240
〜400mm alumina substrate 17 with 1.0〜resistive material
It is applied to 2.5 mm and is energized from both ends. The energization is given by changing the pulse width according to the amount of energy released, the temperature controlled by the temperature sensor 16 with a pulse waveform of DC 100V with a cycle of 25 msec. In the case of the temperature T1 detected by the temperature sensor 16 in the low heat capacity linear heating element 15, the surface temperature T2 of the film material 14 facing the resistance material is lower than the temperature T1.
Here, the temperature T1 is preferably 110 to 220 ° C., and the temperature T2 is preferably 0.5 to 10 ° C. lower than the temperature T1. The film material surface temperature T3 at the portion where the film material 14 is peeled off from the toner fixing surface is almost equal to T2. In this way, the film material moves in the same direction as the recording material by coming into contact with the heating element whose energy and temperature are controlled. The film material 14 has a thickness of 1
0 to 35 μm heat resistant film, for example, polyester,
The film is preferably a film obtained by coating a release material layer of polyperfluoroalkyl vinyl ether, polyimide or polyether imide with a conductive material added to at least a fluororesin such as Teflon for 5 to 15 μm, and more preferably an endless film material. Generally a total thickness of 10-1
The film material 14 is driven by the film material drive roller 11 and the film material driven roller 12 and tensioned so that the film material 14 is conveyed without wrinkles or twists. The pressure roller 13 has a rubber elastic layer having a high releasability such as silicon rubber, presses the low heat capacity linear heating element 15 through the film material 14 at a total pressure of 2 to 30 kg, and press-rotates in the arrow direction. By passing the recording material carrying the toner image between the film material 14 and the pressure roller 13, the low heat capacity linear heating element 15 is passed to melt and fix the toner image on the recording material.
【0033】図2において、図1に示した場合と同様に
含浸ローラー8がフィルム材14の長手方向に渡って、
それを介してフィルム材従動ローラー12に圧接し、矢
印方向に回転している。図2において、フィルム材14
の移動に従って極少量ずつ含浸ローラー8からフィルム
材14の表面に含フッ素系シリコンオイルが供給され
て、その結果フィルム材14の加圧ローラー13側表面
上には本発明の含フッ素系シリコンオイル塗膜が形成さ
れる。In FIG. 2, the impregnating roller 8 extends in the longitudinal direction of the film material 14 as in the case shown in FIG.
It is pressed against the film material driven roller 12 through it and is rotated in the direction of the arrow. In FIG. 2, the film material 14
The fluorine-containing silicone oil is supplied to the surface of the film material 14 from the impregnating roller 8 little by little in accordance with the movement of the film. A film is formed.
【0034】後者の定着方法の他の例を図3を用いて説
明する。この図3の例は、図2の例が、フィルム材がエ
ンドレスであったのに対し、有端なフィルム材の例であ
る。Another example of the latter fixing method will be described with reference to FIG. The example of FIG. 3 is an example of a film material having an end, whereas the example of FIG. 2 is an endless film material.
【0035】即ち、図2の様にシート送り出し軸21及
び巻き取り軸22に有端フィルム材24を巻き付け、定
着毎に少しずつフィルム材24を矢印方向へ移動させ
る。この場合は巻き取り軸22で駆動する。13,1
5,16,17は図2のそれらと同じである。That is, as shown in FIG. 2, the end film material 24 is wound around the sheet feeding shaft 21 and the winding shaft 22, and the film material 24 is gradually moved in the direction of the arrow for each fixing. In this case, the winding shaft 22 drives. 13, 1
5, 16 and 17 are the same as those in FIG.
【0036】巻き取り軸22で駆動により送り出し軸2
1に巻き取られていた有端フィルム材24は定着毎に少
しずつ駆り出され、この有端フィルム材24と加圧ロー
ラー13との間をトナー像を担持した記録材を通過さ
せ、低熱容量ライン状加熱体15を通過させることによ
ってトナー像を記録材に溶融固着させる。The feeding shaft 2 is driven by the winding shaft 22.
The edged film material 24 wound around 1 is ejected little by little at each fixing, and the recording material carrying the toner image is passed between the edged film material 24 and the pressure roller 13, and the low heat capacity line The toner image is melted and fixed to the recording material by passing through the heating element 15.
【0037】図3において、本発明の含フッ素系シリコ
ンオイルを含浸させた含浸ローラー(図示せず)を、シ
ート送り出し軸21へ有端フィルム材24を介して圧接
させ、有端フィルム材の加圧ローラー側表面に本発明の
含フッ素系シリコンオイル塗膜が形成される。In FIG. 3, an impregnating roller (not shown) impregnated with the fluorine-containing silicone oil of the present invention is brought into pressure contact with the sheet delivery shaft 21 via the end film material 24 to apply the end film material. The fluorine-containing silicone oil coating film of the present invention is formed on the surface of the pressure roller side.
【0038】図示した例においては含浸ローラーを使用
した含フッ素系シリコンオイル塗膜形成方法を開示した
が、その他に含フッ素系シリコンオイルを含浸させたパ
ッド、ウェッブ等を使用してもよい。In the illustrated example, a method for forming a fluorine-containing silicone oil coating film using an impregnating roller is disclosed, but a pad, a web or the like impregnated with fluorine-containing silicone oil may be used.
【0039】2.記録材の構成 本発明の記録材は、前述した炭酸カルシウムを含有した
転写紙である。2. Structure of Recording Material The recording material of the present invention is the above-mentioned transfer paper containing calcium carbonate.
【0040】本発明で使用される炭酸カルシウムはタル
クやカオリン等と比較して正帯電性を有しており、紙が
搬送される際の摩擦や感光体との摩擦帯電によって正帯
電が炭酸カルシウムに付与され、効果として紙自体が正
帯電性化されるものと推定される。更に、帯電性の変化
が無く好ましく、この理由はタルクやカオリンと比較し
て炭酸カルシウムは結晶水を含有する事がなく、環境変
動で水分を吸水することが無いためと推定される。The calcium carbonate used in the present invention has a positive electrification property as compared with talc, kaolin and the like, and the positive electrification is calcium carbonate due to friction when the paper is conveyed and frictional electrification with the photoconductor. It is presumed that the paper itself becomes positively charged as an effect. Further, there is no change in chargeability, which is preferable, and it is presumed that calcium carbonate does not contain water of crystallization as compared with talc and kaolin and does not absorb water due to environmental changes.
【0041】炭酸カルシウムが帯電性を発生するメカニ
ズムは明確でないが、感光体等との相互摩擦或いは紙同
士の摩擦帯電によるものと推定される。本発明におい
て、数平均一次粒子径が0.1〜3.0μmであること
が必要であるが炭酸カルシウムは硬度が高いため、数平
均一次粒子径3.0μmを越える炭酸カルシウムを用い
た場合には帯電の発生効果は高いが、感光体を傷つけや
すくなり、画像欠陥を発生する問題を有すること、ま
た、数平均一次粒子径で0.1μm未満の炭酸カルシウ
ムは摩擦帯電性が低下し、正帯電性付与効果が減少する
ためと推定される。Although the mechanism by which calcium carbonate generates charging properties is not clear, it is presumed that it is due to mutual friction with the photoconductor or the like or frictional charging between papers. In the present invention, it is necessary that the number average primary particle diameter is 0.1 to 3.0 μm, but since calcium carbonate has high hardness, when calcium carbonate having a number average primary particle diameter of more than 3.0 μm is used, Has a high effect of charging, but has a problem that it easily damages the photoreceptor and causes image defects, and that calcium carbonate having a number average primary particle diameter of less than 0.1 μm lowers the triboelectric charging property. It is presumed that this is because the effect of imparting electrostatic properties is reduced.
【0042】この数平均一次粒子径は走査型電子顕微鏡
観察で10000倍に拡大し画像解析装置で測定された
値を示す。The number average primary particle diameter is a value measured with an image analyzer after being magnified 10,000 times by observation with a scanning electron microscope.
【0043】炭酸カルシウムの転写紙中の含有量は、
2.0〜10.0重量%が好ましい。特に好ましくは
3.0〜8.0%である。含有量が10.0重量%を越
えると炭酸カルシウムの遊離が過多となり、感光体の研
磨量が増加し耐久性の低下の問題を発生する。一方で添
加量が2.0%重量未満であると感光体に対する付着量
が少なくなり、感光体の研磨効果が低くなることがあ
る。The content of calcium carbonate in the transfer paper is
2.0 to 10.0% by weight is preferable. Particularly preferably, it is 3.0 to 8.0%. If the content exceeds 10.0% by weight, the liberation of calcium carbonate becomes excessive, the polishing amount of the photoconductor increases, and the durability deteriorates. On the other hand, if the addition amount is less than 2.0% by weight, the amount attached to the photoconductor is reduced, and the polishing effect of the photoconductor may be reduced.
【0044】炭酸カルシウムとしては通常の石灰岩を解
砕して得られる重質炭酸カルシウムと生石灰と炭酸ガス
とから調製される軽質炭酸カルシウムがあるが、重質炭
酸カルシウムは形状が不定形であるため感光体に対して
傷を発生しやすいことから、軽質炭酸カルシウムが好ま
しい。この場合、粒子の形状としては紡錘状、針状、粒
状等種々のものが得られるが、何れも不定形の形状では
ないことから、感光体に対する傷の発生がなく好まし
い。As calcium carbonate, there are heavy calcium carbonate obtained by crushing ordinary limestone and light calcium carbonate prepared from quicklime and carbon dioxide, but since heavy calcium carbonate has an indefinite shape. Light calcium carbonate is preferable because it easily scratches the photoreceptor. In this case, various particles such as a spindle shape, a needle shape, and a granular shape can be obtained. However, none of them has an irregular shape, which is preferable because no scratch is generated on the photoreceptor.
【0045】紙を構成するために使用されるパルプとし
ては広葉樹から得られるパルプ及び針葉樹から得られる
パルプ、更には脱墨して得られる古紙パルプの何れを使
用しても良い。しかし、フルカラー面像を形成するため
には紙として白色度の高い紙が高い品位をえることがで
きるため、広葉樹から得られるパルプが好ましい。As the pulp used for constituting the paper, any of pulp obtained from hardwood, pulp obtained from softwood, and waste paper pulp obtained by deinking may be used. However, in order to form a full-color surface image, a paper having a high whiteness can be obtained as a high quality paper, and thus a pulp obtained from hardwood is preferable.
【0046】転写紙には、上記炭酸カルシウムの他、公
知の添加剤が使用される。In addition to the above calcium carbonate, known additives are used in the transfer paper.
【0047】例えば、紙中に添加されるサイズ剤として
はアルケニルコハク酸無水物、アルキルケテンダイマ
ー、脂肪酸無水物、イソシアナートアジリジン誘導体が
あげられる。Examples of the sizing agent added to the paper include alkenyl succinic anhydride, alkyl ketene dimer, fatty acid anhydride, and isocyanate aziridine derivative.
【0048】紙の物性としては表面の抵抗を22℃/6
5%環境下で放置後に1×109〜1×1012Ωとする
ことが好ましい(JIS−C−211)。平滑度は表面
(ワイヤー面)で21秒〜40秒とする事が好ましい
(JIS−P−8119)。紙中に存在する水分量はカ
ールの影響を小さくするために、4.0〜6.0%に調
整されていることが好ましい(JIS−P−812
5)。更に、白色度は80〜90%が好ましい(JIS
−P−8128)。As the physical properties of paper, the surface resistance is 22 ° C./6.
It is preferably set to 1 × 10 9 to 1 × 10 12 Ω after standing in a 5% environment (JIS-C-211). The smoothness is preferably 21 seconds to 40 seconds on the surface (wire surface) (JIS-P-8119). The amount of water present in the paper is preferably adjusted to 4.0 to 6.0% in order to reduce the influence of curling (JIS-P-812.
5). Further, the whiteness is preferably 80 to 90% (JIS
-P-8128).
【0049】3.現像剤の構成 本発明のトナーは特に限定されない。平均粒径は体積平
均粒径で1〜30μmが好ましく、更に好ましくは5〜
20μmである。トナーを構成する結着樹脂としては特
に限定されず、従来公知の種々の樹脂が用いられる。例
えば、スチレン系樹脂、アクリル系樹脂、スチレン/ア
クリル系樹脂、ポリエステル樹脂等が挙げられる。トナ
ーを構成する着色剤としては特に限定されず、従来公知
の種々の材料が使用される。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、カルコイルブルー、
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ライ
ド、フタロシアニンブルー、マラカイトグリーンオクサ
レート、ローズベンガル等が挙げられる。その他の添加
剤としては例えばサリチル酸誘導体、アゾ系金属錯体等
の荷電制御剤等が挙げられる。また、磁性トナーを得る
場合には着色粒子に添加剤として磁性体粒子が含有され
る。磁性体粒子としては平均一次粒子径が0.1〜2.
0μmのフェライト・マグネタイト等の粒子が好ましく
用いられる。磁性体粒子の添加量は着色粒子中の20〜
70重量%であることが好ましい。3. Structure of Developer The toner of the present invention is not particularly limited. The volume average particle diameter is preferably 1 to 30 μm, more preferably 5 to
It is 20 μm. The binder resin that constitutes the toner is not particularly limited, and various conventionally known resins can be used. For example, a styrene resin, an acrylic resin, a styrene / acrylic resin, a polyester resin, and the like can be given. The colorant that constitutes the toner is not particularly limited, and various conventionally known materials are used. For example, carbon black,
Nigrosine dye, aniline blue, calcoil blue,
Examples include chrome yellow, ultramarine blue, DuPont oil red, quinoline yellow, methylene blue chloride, phthalocyanine blue, malachite green oxalate, and rose bengal. Examples of other additives include salicylic acid derivatives, charge control agents such as azo metal complexes, and the like. Further, when a magnetic toner is obtained, magnetic particles are added to the colored particles as an additive. The magnetic particles have an average primary particle diameter of 0.1 to 2.
Particles of 0 .mu.m ferrite, magnetite or the like are preferably used. The amount of the magnetic particles added is 20 to 20% of the colored particles.
Preferably, it is 70% by weight.
【0050】また、流動性付与の観点から、無機微粒子
を添加してもよい。無機微粒子としてはシリカ、チタニ
ア、アルミナ等の無機酸化物粒子が好ましく、更に、こ
れら無機微粒子はシランカップリング剤やチタンカップ
リング剤等によって疎水化処理されていることが好まし
い。From the viewpoint of imparting fluidity, inorganic fine particles may be added. As the inorganic fine particles, inorganic oxide particles such as silica, titania, and alumina are preferable, and these inorganic fine particles are preferably subjected to a hydrophobic treatment with a silane coupling agent, a titanium coupling agent, or the like.
【0051】トナーはキャリアと混合され、二成分現像
剤として使用されるか、或いは磁性トナーである場合は
該磁性トナーのみにより一成分現像剤として使用され
る。The toner is mixed with a carrier and used as a two-component developer or, in the case of a magnetic toner, only the magnetic toner is used as a one-component developer.
【0052】二成分現像剤を構成するキャリアとしては
鉄、フェライト等の磁性材料粒子のみで構成される非被
覆キャリア、磁性材料粒子表面を樹脂等によって被覆し
た樹脂被覆キャリアの何れを使用してもよい。このキャ
リアの平均粒径は体積平均粒径で30〜150μmが好
ましい。As the carrier constituting the two-component developer, either an uncoated carrier composed only of magnetic material particles such as iron or ferrite, or a resin coated carrier in which the magnetic material particle surfaces are coated with a resin or the like is used. Good. The average particle size of the carrier is preferably 30 to 150 μm in volume average particle size.
【0053】一方で離型剤を添加してもよい。この離型
剤としては低分子量ポリオレフィン類、脂肪酸アミド
類、天然ワックス類等があげられる。これらの添加量は
トナー中に1〜5重量%添加されていることが好まし
い。On the other hand, a release agent may be added. Examples of the releasing agent include low molecular weight polyolefins, fatty acid amides and natural waxes. The addition amount of these is preferably 1 to 5% by weight in the toner.
【0054】[0054]
【実施例】以下、実施例を挙げて本発明を詳細に説明す
るが、本発明の態様はこれに限定されない。The present invention will be described in detail below with reference to examples, but the embodiments of the present invention are not limited thereto.
【0055】紙製造例1 下記表に示す配合で紙を調製した。Paper Production Example 1 Paper was prepared with the formulations shown in the table below.
【0056】[0056]
【表1】 [Table 1]
【0057】[0057]
【表2】 [Table 2]
【0058】(現像剤製造例)ポリエステル樹脂(PE
S)100部、カーボンブラック5部、低分子量ポリプ
ロピレン3部を加えて熔融、混練を行い、粉砕分級した
後に体積平均粒径が8.3μmの着色粒子を得た。つい
で、このものに疎水性シリカを0.8%添加しトナーを
得た。(Production Example of Developer) Polyester Resin (PE
S) 100 parts, carbon black 5 parts, and low molecular weight polypropylene 3 parts were added, and the mixture was melted and kneaded, and pulverized and classified to obtain colored particles having a volume average particle diameter of 8.3 μm. Then, 0.8% of hydrophobic silica was added to this product to obtain a toner.
【0059】また、これらトナーに対してスチレン−ア
クリル樹脂を被覆した体積平均粒径が62μmのフェラ
イトキャリアを混合し、トナー濃度が7重量%である現
像剤を調製した。Further, a styrene-acrylic resin-coated ferrite carrier having a volume average particle size of 62 μm was mixed with these toners to prepare a developer having a toner concentration of 7% by weight.
【0060】*評価機としてコニカ(株)製複写機コニ
カ3035を改造した図1に示したものと概要が同じ定
着器を使用した。下記に定着条件に関する改造内容を示
す。A fixing device having the same outline as that shown in FIG. 1, which is a modified copy machine Konica 3035 manufactured by Konica Corporation, was used as an evaluation machine. Below are the details of the modification related to the fixing conditions.
【0061】なお、上記評価紙はA4に調整して使用し
た。The evaluation paper was used after being adjusted to A4 size.
【0062】・熱ローラー定着条件 熱ローラー方式として、表面2をテトラフルオロエチレ
ン−パーフルオロアルキルビニルエーテル共重合体で被
覆した直径30mmφの加熱源4を中央部に内蔵した円
柱状の鉄を上ローラー1として有し、表面が同様にテト
ラフルオロエチレン−パーフルオロアルキルエーテル共
重合体で被覆したシリコンゴムで構成された直径30m
mφの下ローラー5を有している。線圧は0.8kg/
cmに設定され、ニップの幅は4.3mmとした。この
定着器を使用して、印字の線達を250mm/secに
設定した。なお、定着器のクリーニング機構としては以
下の本発明の含フッ素系シリコンオイル例示化合物を含
浸した含浸ローラー8を装着して使用した。例示化合物
(3)、(7)、(8)、(9)を用い、これら熱ロー
ラー状定着装置をR−1、R−2、R−3、R−4とす
る。Heat roller fixing conditions As a heat roller method, a cylindrical iron having a heating source 4 having a diameter of 30 mm and having a surface 2 coated with a tetrafluoroethylene-perfluoroalkyl vinyl ether copolymer in the central portion is used as the upper roller 1. The diameter of which is 30 m and which is composed of silicone rubber whose surface is also coated with a tetrafluoroethylene-perfluoroalkyl ether copolymer.
It has a lower roller 5 of mφ. Linear pressure is 0.8 kg /
cm, and the width of the nip was 4.3 mm. This fixing device was used to set the printing stroke to 250 mm / sec. As the cleaning mechanism of the fixing device, the impregnating roller 8 impregnated with the fluorine-containing silicone oil exemplified compound of the present invention was attached and used. Using the exemplified compounds (3), (7), (8) and (9), these heat roller fixing devices are designated as R-1, R-2, R-3 and R-4.
【0063】また、定着器は、上ローラー1の表面温度
を可変(110〜230℃)できるものを用いた。As the fixing device, one which can change the surface temperature of the upper roller 1 (110 to 230 ° C.) was used.
【0064】・フィルム定着条件 定着装置を図2に示す、エンドレスシート定着器(フィ
ルム定着装置)を用い、定着の条件を下記に設定した。Film Fixing Conditions The fixing conditions were set as follows using the endless sheet fixing device (film fixing device) shown in FIG.
【0065】定着条件:加熱体15の温度T1=110
〜230℃ フィルム材14の移動速度=250mm/sec 加熱体15・加圧ローラー13間層圧=15kg 加圧ローラー13・フィルム材14間ニップ=3mm フィルム材14:表面に導電性物質を分散したポリテト
ラフルオロエチレンを被覆した厚みがl5umのポリイ
ミドフィルム材 なお、定着器のクリーニング機構としては以下の本発明
の含フッ素系シリコンオイル例示化合物を含浸した含浸
ローラー8を装着して使用した。例示化合物(3)、
(7)、(8)、(9)を用い、これらフィルム定着装
置をF−1、F−2、F−3、F−4とする。Fixing condition: Temperature T1 of heating element 15 = 110
~ 230 ° C Moving speed of film material 14 = 250 mm / sec Layer pressure between heating element 15 and pressure roller 13 = 15 kg Nip between pressure roller 13 and film material 14 = 3 mm Film material 14: Conductive substance dispersed on surface A polyimide film material having a thickness of 15 um and coated with polytetrafluoroethylene was used. As a cleaning mechanism of the fixing device, an impregnating roller 8 impregnated with the following compound of the fluorine-containing silicone oil of the present invention was mounted and used. Exemplified compound (3),
Using (7), (8), and (9), these film fixing devices are designated as F-1, F-2, F-3, and F-4.
【0066】一方、比較用定着装置として、ジメチルポ
リシロキサンからなるシリコンオイル(ジメチルシリコ
ンオイル)を前述の含浸ローラー8に含浸したものと、
特開昭52−124338号に記載されている側鎖のフ
ッ化アルキルが単なるトリフルオロメチルであるフッ素
系シリコンオイル(FS−1265:ダウコーニング社
製)を含浸ローラー8に含浸したものを使用した。ジメ
チルシリコンオイル使用熱ローラー状定着装置をR−比
1、フィルム定着装置をF−比1とし、本発明外のフッ
素系シリコンオイルを用いた定着装置をそれぞれ、R−
比2、F−比2とする。On the other hand, as a comparative fixing device, a device in which the above-mentioned impregnating roller 8 is impregnated with silicone oil (dimethyl silicone oil) made of dimethylpolysiloxane,
The impregnation roller 8 was impregnated with a fluorine-based silicone oil (FS-1265: manufactured by Dow Corning Co., Ltd.) in which the side chain alkyl fluoride described in JP-A-52-124338 is simply trifluoromethyl. . The heat roller type fixing device using dimethyl silicone oil has an R-ratio of 1, the film fixing device has an F-ratio of 1, and a fixing device using a fluorine-based silicone oil other than the present invention is R-ratio.
Ratio 2 and F-ratio 2.
【0067】(評価) ・定着率評価 定着率は上記現像剤を用いてベタ黒面像を現像しその後
前述の本発明及び比較用紙に対して転写を行い、10℃
/10%RHの環境下で、定着温度を5℃単位で120
℃〜200℃まで定着温度を変化させた上記定着装置を
用いて定着し、測定を行った。測定は定着された画像を
折り曲げ、その後に摩擦堅牢度試験器を用いて布で摩擦
を10回繰り返し、その前後の反射濃度をRD−918
にて測定し、その差から下記式に従って定着率を測定し
た。なお、初期画像濃度は紙の濃度を0とした相対反射
濃度で1.40に調整して測定を実施した。(Evaluation) Evaluation of Fixing Rate The fixing rate was 10 ° C. by developing a solid black surface image using the above-mentioned developer and then transferring to the above-mentioned invention and comparative paper.
/ 10% RH environment, fixing temperature 120 in 5 ℃ increments
The fixing was carried out using the above fixing device in which the fixing temperature was changed from ℃ to 200 ℃, and the measurement was carried out. For the measurement, the fixed image was bent, and thereafter, rubbing with a cloth was repeated 10 times using a friction fastness tester, and the reflection density before and after the rubbing was measured with RD-918.
And the fixing ratio was measured from the difference according to the following formula. The initial image density was adjusted to 1.40 by the relative reflection density with the density of the paper being 0, and the measurement was performed.
【0068】[0068]
【数1】 [Equation 1]
【0069】定着率が70%以上であると実用上問題無
いレベルであることから、この定着率になる定着装置の
表面温度を評価した。下記表に70%の定着率を示す温
度を示す。更に画素率2%の画像を低温低湿環境(10
℃/20%RH)にて5万枚の印字を行い、定着ローラ
ー或いはフィルムの傷の有無を判定した。下記表に傷の
有無について目視で判定した結果を示す。傷があるもの
を×、傷の発生の無いものを○で評価した。When the fixing rate is 70% or more, there is no problem in practical use. Therefore, the surface temperature of the fixing device having this fixing rate was evaluated. The table below shows the temperatures at which a fixing ratio of 70% is obtained. Furthermore, an image with a pixel ratio of 2% is displayed in a low temperature and low humidity environment (10
Printing was performed on 50,000 sheets at (° C./20% RH), and the presence or absence of scratches on the fixing roller or the film was determined. The following table shows the results of visual judgment for the presence of scratches. Those with scratches were evaluated as x, and those without scratches were evaluated as o.
【0070】[0070]
【表3】 [Table 3]
【0071】[0071]
【表4】 [Table 4]
【0072】[0072]
【発明の効果】本発明による熱定着方法は含フッ素系シ
リコンオイルを用いた熱定着方法において、定着部での
静電的な反発による、紙の定着装置対する密着性の低下
が無く、定着効率に優れ且つ、定着ローラー及びフィル
ム傷の発生の無い優れた効果を示す。The heat fixing method according to the present invention is a heat fixing method using a fluorine-containing silicone oil, and the fixing efficiency of the paper does not deteriorate due to electrostatic repulsion at the fixing section. It also has an excellent effect in that it does not cause the fixing roller and film scratches.
【図1】本発明の一例を示す熱ローラー定着方法の概略
構成例を示す図である。FIG. 1 is a diagram showing a schematic configuration example of a heat roller fixing method showing an example of the present invention.
【図2】本発明の他の一例であるフィルム材を介して加
熱体と記録材とを接触させる熱定着方法の概略構成例を
示す図である。FIG. 2 is a diagram showing a schematic configuration example of a heat fixing method of bringing a heating body and a recording material into contact with each other via a film material which is another example of the present invention.
【図3】図2に示した熱定着方法の変形例を示す概略構
成例を示す図である。FIG. 3 is a diagram showing a schematic configuration example showing a modification of the heat fixing method shown in FIG.
1 上ローラー 4 加熱源 5 下ローラー 6 記録材 8 含浸ローラー 11 フィルム材駆動ローラー 12 フィルム材従動ローラー 14 フィルム材 15 低熱容量ライン状加熱体 1 Upper Roller 4 Heating Source 5 Lower Roller 6 Recording Material 8 Impregnation Roller 11 Film Material Drive Roller 12 Film Material Driven Roller 14 Film Material 15 Low Heat Capacity Linear Heating Body
Claims (2)
る記録材を圧接する圧着部材及び該定着部材を介して、
該記録材上のトナー像を熱熔融する加熱手段を設けてな
る熱定着方法において、前記定着部材の記録材と接触す
る側の表面に、下記一般式〔I〕で示される構造単位を
有する含フッ素系シリコンオイル塗膜を形成し、且つ記
録材が数平均一次粒子径0.1〜3.0μmの炭酸カル
シウムを含有することを特徴とする熱定着方法。 【化1】 〔式中、Xは炭素数1〜4の飽和炭化水素基又はアリー
ル基を示し、Rfは炭素原子数2〜10のフルオロアル
キル基を示し、nは1〜4の整数を示す。〕1. A moving fixing member, a pressure-bonding member for pressing a recording material moving to the fixing member, and the fixing member,
In a thermal fixing method comprising a heating means for thermally melting a toner image on the recording material, the surface of the fixing member in contact with the recording material contains a structural unit represented by the following general formula [I]. A heat fixing method, wherein a fluorine-based silicone oil coating film is formed, and the recording material contains calcium carbonate having a number average primary particle diameter of 0.1 to 3.0 μm. Embedded image [In the formula, X represents a saturated hydrocarbon group having 1 to 4 carbon atoms or an aryl group, R f represents a fluoroalkyl group having 2 to 10 carbon atoms, and n represents an integer of 1 to 4. ]
た定着ローラーであることを特徴とする請求項1記載の
熱定着方法。2. The heat fixing method according to claim 1, wherein the fixing member is a fixing roller having the heating unit built therein.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP18688195A JPH0934285A (en) | 1995-07-24 | 1995-07-24 | Heat fixing method |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP18688195A JPH0934285A (en) | 1995-07-24 | 1995-07-24 | Heat fixing method |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| JPH0934285A true JPH0934285A (en) | 1997-02-07 |
Family
ID=16196321
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP18688195A Pending JPH0934285A (en) | 1995-07-24 | 1995-07-24 | Heat fixing method |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPH0934285A (en) |
-
1995
- 1995-07-24 JP JP18688195A patent/JPH0934285A/en active Pending
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