JPH04333854A - Production of toner for pressure fixing - Google Patents
Production of toner for pressure fixingInfo
- Publication number
- JPH04333854A JPH04333854A JP3105728A JP10572891A JPH04333854A JP H04333854 A JPH04333854 A JP H04333854A JP 3105728 A JP3105728 A JP 3105728A JP 10572891 A JP10572891 A JP 10572891A JP H04333854 A JPH04333854 A JP H04333854A
- Authority
- JP
- Japan
- Prior art keywords
- toner
- inner core
- resin
- resin particles
- pressure 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
- 238000004519 manufacturing process Methods 0.000 title claims description 14
- 229920005989 resin Polymers 0.000 claims abstract description 82
- 239000011347 resin Substances 0.000 claims abstract description 82
- 239000002245 particle Substances 0.000 claims abstract description 67
- 239000011247 coating layer Substances 0.000 claims abstract description 30
- 239000002904 solvent Substances 0.000 claims abstract description 21
- 238000000034 method Methods 0.000 claims abstract description 20
- 238000009826 distribution Methods 0.000 claims abstract description 6
- 238000007639 printing Methods 0.000 claims description 9
- 239000000463 material Substances 0.000 claims description 8
- 238000004040 coloring Methods 0.000 claims description 6
- 238000003825 pressing Methods 0.000 claims description 2
- 230000002776 aggregation Effects 0.000 abstract description 7
- 238000004220 aggregation Methods 0.000 abstract description 6
- 239000003086 colorant Substances 0.000 abstract description 5
- 230000015572 biosynthetic process Effects 0.000 abstract 1
- 239000002356 single layer Substances 0.000 abstract 1
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 9
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 9
- -1 polyethylene Polymers 0.000 description 8
- 239000001993 wax Substances 0.000 description 8
- 238000001694 spray drying Methods 0.000 description 7
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 6
- 229920001577 copolymer Polymers 0.000 description 6
- 239000003094 microcapsule Substances 0.000 description 6
- 239000011248 coating agent Substances 0.000 description 5
- 238000000576 coating method Methods 0.000 description 5
- 238000004898 kneading Methods 0.000 description 5
- 239000010410 layer Substances 0.000 description 5
- 239000000843 powder Substances 0.000 description 5
- 230000000052 comparative effect Effects 0.000 description 4
- 229920000642 polymer Polymers 0.000 description 4
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 3
- WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 description 3
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 3
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 3
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 3
- 241000519995 Stachys sylvatica Species 0.000 description 3
- 239000003795 chemical substances by application Substances 0.000 description 3
- 238000004090 dissolution Methods 0.000 description 3
- 239000010419 fine particle Substances 0.000 description 3
- 239000006247 magnetic powder Substances 0.000 description 3
- 238000002156 mixing Methods 0.000 description 3
- 239000000203 mixture Substances 0.000 description 3
- 239000012188 paraffin wax Substances 0.000 description 3
- 108091008695 photoreceptors Proteins 0.000 description 3
- 229920002037 poly(vinyl butyral) polymer Polymers 0.000 description 3
- 229920000058 polyacrylate Polymers 0.000 description 3
- 229920000193 polymethacrylate Polymers 0.000 description 3
- 150000003839 salts Chemical class 0.000 description 3
- AZQWKYJCGOJGHM-UHFFFAOYSA-N 1,4-benzoquinone Chemical compound O=C1C=CC(=O)C=C1 AZQWKYJCGOJGHM-UHFFFAOYSA-N 0.000 description 2
- PAYRUJLWNCNPSJ-UHFFFAOYSA-N Aniline Chemical compound NC1=CC=CC=C1 PAYRUJLWNCNPSJ-UHFFFAOYSA-N 0.000 description 2
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 2
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 2
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 2
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 2
- 239000004698 Polyethylene Substances 0.000 description 2
- 239000004743 Polypropylene Substances 0.000 description 2
- 239000004793 Polystyrene Substances 0.000 description 2
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
- 229920007962 Styrene Methyl Methacrylate Polymers 0.000 description 2
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 2
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 2
- 239000004359 castor oil Substances 0.000 description 2
- 235000019438 castor oil Nutrition 0.000 description 2
- 239000012461 cellulose resin Substances 0.000 description 2
- MVPPADPHJFYWMZ-UHFFFAOYSA-N chlorobenzene Chemical compound ClC1=CC=CC=C1 MVPPADPHJFYWMZ-UHFFFAOYSA-N 0.000 description 2
- JHIVVAPYMSGYDF-UHFFFAOYSA-N cyclohexanone Chemical compound O=C1CCCCC1 JHIVVAPYMSGYDF-UHFFFAOYSA-N 0.000 description 2
- 239000002270 dispersing agent Substances 0.000 description 2
- 239000006185 dispersion Substances 0.000 description 2
- 238000001035 drying Methods 0.000 description 2
- 150000002148 esters Chemical class 0.000 description 2
- HYBBIBNJHNGZAN-UHFFFAOYSA-N furfural Chemical compound O=CC1=CC=CO1 HYBBIBNJHNGZAN-UHFFFAOYSA-N 0.000 description 2
- ZEMPKEQAKRGZGQ-XOQCFJPHSA-N glycerol triricinoleate Natural products CCCCCC[C@@H](O)CC=CCCCCCCCC(=O)OC[C@@H](COC(=O)CCCCCCCC=CC[C@@H](O)CCCCCC)OC(=O)CCCCCCCC=CC[C@H](O)CCCCCC ZEMPKEQAKRGZGQ-XOQCFJPHSA-N 0.000 description 2
- SZVJSHCCFOBDDC-UHFFFAOYSA-N iron(II,III) oxide Inorganic materials O=[Fe]O[Fe]O[Fe]=O SZVJSHCCFOBDDC-UHFFFAOYSA-N 0.000 description 2
- 150000002576 ketones Chemical class 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- ADFPJHOAARPYLP-UHFFFAOYSA-N methyl 2-methylprop-2-enoate;styrene Chemical compound COC(=O)C(C)=C.C=CC1=CC=CC=C1 ADFPJHOAARPYLP-UHFFFAOYSA-N 0.000 description 2
- 239000004200 microcrystalline wax Substances 0.000 description 2
- 235000019808 microcrystalline wax Nutrition 0.000 description 2
- 239000003595 mist Substances 0.000 description 2
- 239000012170 montan wax Substances 0.000 description 2
- LQNUZADURLCDLV-UHFFFAOYSA-N nitrobenzene Chemical compound [O-][N+](=O)C1=CC=CC=C1 LQNUZADURLCDLV-UHFFFAOYSA-N 0.000 description 2
- 229920001225 polyester resin Polymers 0.000 description 2
- 239000004645 polyester resin Substances 0.000 description 2
- 229920000573 polyethylene Polymers 0.000 description 2
- 229920013716 polyethylene resin Polymers 0.000 description 2
- 229920001155 polypropylene Polymers 0.000 description 2
- 229920002223 polystyrene Polymers 0.000 description 2
- VZGDMQKNWNREIO-UHFFFAOYSA-N tetrachloromethane Chemical compound ClC(Cl)(Cl)Cl VZGDMQKNWNREIO-UHFFFAOYSA-N 0.000 description 2
- 229920005992 thermoplastic resin Polymers 0.000 description 2
- SCYULBFZEHDVBN-UHFFFAOYSA-N 1,1-Dichloroethane Chemical compound CC(Cl)Cl SCYULBFZEHDVBN-UHFFFAOYSA-N 0.000 description 1
- RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 description 1
- XNWFRZJHXBZDAG-UHFFFAOYSA-N 2-METHOXYETHANOL Chemical compound COCCO XNWFRZJHXBZDAG-UHFFFAOYSA-N 0.000 description 1
- DKPFZGUDAPQIHT-UHFFFAOYSA-N Butyl acetate Natural products CCCCOC(C)=O DKPFZGUDAPQIHT-UHFFFAOYSA-N 0.000 description 1
- 239000004215 Carbon black (E152) Substances 0.000 description 1
- VYZAMTAEIAYCRO-UHFFFAOYSA-N Chromium Chemical compound [Cr] VYZAMTAEIAYCRO-UHFFFAOYSA-N 0.000 description 1
- 235000000177 Indigofera tinctoria Nutrition 0.000 description 1
- 238000012695 Interfacial polymerization Methods 0.000 description 1
- 239000004166 Lanolin Substances 0.000 description 1
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 1
- NRCMAYZCPIVABH-UHFFFAOYSA-N Quinacridone Chemical compound N1C2=CC=CC=C2C(=O)C2=C1C=C1C(=O)C3=CC=CC=C3NC1=C2 NRCMAYZCPIVABH-UHFFFAOYSA-N 0.000 description 1
- PJANXHGTPQOBST-VAWYXSNFSA-N Stilbene Natural products C=1C=CC=CC=1/C=C/C1=CC=CC=C1 PJANXHGTPQOBST-VAWYXSNFSA-N 0.000 description 1
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 1
- 239000006230 acetylene black Substances 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 238000005054 agglomeration Methods 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 125000001931 aliphatic group Chemical group 0.000 description 1
- 125000005210 alkyl ammonium group Chemical group 0.000 description 1
- 150000001408 amides Chemical class 0.000 description 1
- 239000012164 animal wax Substances 0.000 description 1
- 239000003945 anionic surfactant Substances 0.000 description 1
- PYKYMHQGRFAEBM-UHFFFAOYSA-N anthraquinone Natural products CCC(=O)c1c(O)c2C(=O)C3C(C=CC=C3O)C(=O)c2cc1CC(=O)OC PYKYMHQGRFAEBM-UHFFFAOYSA-N 0.000 description 1
- 150000004056 anthraquinones Chemical class 0.000 description 1
- 235000013871 bee wax Nutrition 0.000 description 1
- 239000012166 beeswax Substances 0.000 description 1
- HFACYLZERDEVSX-UHFFFAOYSA-N benzidine Chemical compound C1=CC(N)=CC=C1C1=CC=C(N)C=C1 HFACYLZERDEVSX-UHFFFAOYSA-N 0.000 description 1
- 230000005540 biological transmission Effects 0.000 description 1
- 239000004204 candelilla wax Substances 0.000 description 1
- 235000013868 candelilla wax Nutrition 0.000 description 1
- 229940073532 candelilla wax Drugs 0.000 description 1
- 239000006229 carbon black Substances 0.000 description 1
- 235000019241 carbon black Nutrition 0.000 description 1
- 150000001735 carboxylic acids Chemical class 0.000 description 1
- 239000004203 carnauba wax Substances 0.000 description 1
- 235000013869 carnauba wax Nutrition 0.000 description 1
- 239000003093 cationic surfactant Substances 0.000 description 1
- 239000006231 channel black Substances 0.000 description 1
- 229910052804 chromium Inorganic materials 0.000 description 1
- 239000011651 chromium Substances 0.000 description 1
- 239000000084 colloidal system 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
- 230000007547 defect Effects 0.000 description 1
- 238000010586 diagram Methods 0.000 description 1
- MHDVGSVTJDSBDK-UHFFFAOYSA-N dibenzyl ether Chemical compound C=1C=CC=CC=1COCC1=CC=CC=C1 MHDVGSVTJDSBDK-UHFFFAOYSA-N 0.000 description 1
- 235000014113 dietary fatty acids Nutrition 0.000 description 1
- HPNMFZURTQLUMO-UHFFFAOYSA-N diethylamine Chemical compound CCNCC HPNMFZURTQLUMO-UHFFFAOYSA-N 0.000 description 1
- PPSZHCXTGRHULJ-UHFFFAOYSA-N dioxazine Chemical compound O1ON=CC=C1 PPSZHCXTGRHULJ-UHFFFAOYSA-N 0.000 description 1
- 238000007599 discharging Methods 0.000 description 1
- 238000012674 dispersion polymerization Methods 0.000 description 1
- 239000000975 dye Substances 0.000 description 1
- 238000007720 emulsion polymerization reaction Methods 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 239000005038 ethylene vinyl acetate Substances 0.000 description 1
- 239000000194 fatty acid Substances 0.000 description 1
- 229930195729 fatty acid Natural products 0.000 description 1
- 150000004665 fatty acids Chemical class 0.000 description 1
- 238000001914 filtration Methods 0.000 description 1
- 239000012530 fluid Substances 0.000 description 1
- 238000000227 grinding Methods 0.000 description 1
- 150000008282 halocarbons Chemical class 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- IUJAMGNYPWYUPM-UHFFFAOYSA-N hentriacontane Chemical compound CCCCCCCCCCCCCCCCCCCCCCCCCCCCCCC IUJAMGNYPWYUPM-UHFFFAOYSA-N 0.000 description 1
- FUZZWVXGSFPDMH-UHFFFAOYSA-N hexanoic acid Chemical compound CCCCCC(O)=O FUZZWVXGSFPDMH-UHFFFAOYSA-N 0.000 description 1
- 229930195733 hydrocarbon Natural products 0.000 description 1
- 150000002430 hydrocarbons Chemical class 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 229940097275 indigo Drugs 0.000 description 1
- COHYTHOBJLSHDF-UHFFFAOYSA-N indigo powder Natural products N1C2=CC=CC=C2C(=O)C1=C1C(=O)C2=CC=CC=C2N1 COHYTHOBJLSHDF-UHFFFAOYSA-N 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- 235000019388 lanolin Nutrition 0.000 description 1
- 229940039717 lanolin Drugs 0.000 description 1
- 239000000696 magnetic material Substances 0.000 description 1
- 239000012184 mineral wax Substances 0.000 description 1
- LKKPNUDVOYAOBB-UHFFFAOYSA-N naphthalocyanine Chemical compound N1C(N=C2C3=CC4=CC=CC=C4C=C3C(N=C3C4=CC5=CC=CC=C5C=C4C(=N4)N3)=N2)=C(C=C2C(C=CC=C2)=C2)C2=C1N=C1C2=CC3=CC=CC=C3C=C2C4=N1 LKKPNUDVOYAOBB-UHFFFAOYSA-N 0.000 description 1
- 229910052759 nickel Inorganic materials 0.000 description 1
- 150000004767 nitrides Chemical class 0.000 description 1
- 229910017464 nitrogen compound Inorganic materials 0.000 description 1
- 150000002830 nitrogen compounds Chemical class 0.000 description 1
- 239000002736 nonionic surfactant Substances 0.000 description 1
- 125000002524 organometallic group Chemical group 0.000 description 1
- 125000002080 perylenyl group Chemical group C1(=CC=C2C=CC=C3C4=CC=CC5=CC=CC(C1=C23)=C45)* 0.000 description 1
- CSHWQDPOILHKBI-UHFFFAOYSA-N peryrene Natural products C1=CC(C2=CC=CC=3C2=C2C=CC=3)=C3C2=CC=CC3=C1 CSHWQDPOILHKBI-UHFFFAOYSA-N 0.000 description 1
- 239000012169 petroleum derived wax Substances 0.000 description 1
- 235000019381 petroleum wax Nutrition 0.000 description 1
- 238000005191 phase separation Methods 0.000 description 1
- IEQIEDJGQAUEQZ-UHFFFAOYSA-N phthalocyanine Chemical compound N1C(N=C2C3=CC=CC=C3C(N=C3C4=CC=CC=C4C(=N4)N3)=N2)=C(C=CC=C2)C2=C1N=C1C2=CC=CC=C2C4=N1 IEQIEDJGQAUEQZ-UHFFFAOYSA-N 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 229920001200 poly(ethylene-vinyl acetate) Polymers 0.000 description 1
- 125000003367 polycyclic group Chemical group 0.000 description 1
- 238000006116 polymerization reaction Methods 0.000 description 1
- 238000010298 pulverizing process Methods 0.000 description 1
- HNJBEVLQSNELDL-UHFFFAOYSA-N pyrrolidin-2-one Chemical compound O=C1CCCN1 HNJBEVLQSNELDL-UHFFFAOYSA-N 0.000 description 1
- WVIICGIFSIBFOG-UHFFFAOYSA-N pyrylium Chemical compound C1=CC=[O+]C=C1 WVIICGIFSIBFOG-UHFFFAOYSA-N 0.000 description 1
- 238000004904 shortening Methods 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 239000007779 soft material Substances 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 239000007921 spray Substances 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- PJANXHGTPQOBST-UHFFFAOYSA-N stilbene Chemical compound C=1C=CC=CC=1C=CC1=CC=CC=C1 PJANXHGTPQOBST-UHFFFAOYSA-N 0.000 description 1
- 235000021286 stilbenes Nutrition 0.000 description 1
- 238000010557 suspension polymerization reaction Methods 0.000 description 1
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 1
- 150000003568 thioethers Chemical class 0.000 description 1
- JOUDBUYBGJYFFP-FOCLMDBBSA-N thioindigo Chemical compound S\1C2=CC=CC=C2C(=O)C/1=C1/C(=O)C2=CC=CC=C2S1 JOUDBUYBGJYFFP-FOCLMDBBSA-N 0.000 description 1
- ANRHNWWPFJCPAZ-UHFFFAOYSA-M thionine Chemical compound [Cl-].C1=CC(N)=CC2=[S+]C3=CC(N)=CC=C3N=C21 ANRHNWWPFJCPAZ-UHFFFAOYSA-M 0.000 description 1
- OGIDPMRJRNCKJF-UHFFFAOYSA-N titanium oxide Inorganic materials [Ti]=O OGIDPMRJRNCKJF-UHFFFAOYSA-N 0.000 description 1
- 239000012178 vegetable wax Substances 0.000 description 1
- 239000008096 xylene Substances 0.000 description 1
- 229910000859 α-Fe Inorganic materials 0.000 description 1
Landscapes
- Developing Agents For Electrophotography (AREA)
Abstract
Description
【0001】0001
【産業上の利用分野】本発明は電子写真法により画像を
形成するプリンター、複写機、ファクシミリ等に用いる
トナーの製造方法に関し、特に圧力定着用トナーの製造
方法に関する。BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a method for producing toner for use in printers, copying machines, facsimile machines, etc. that form images by electrophotography, and particularly relates to a method for producing toner for pressure fixing.
【0002】0002
【従来の技術】従来、電子写真法としては米国特許第2
297691号、米国特許第2874063号、特公昭
42−23910号公報、特公昭43−24748号公
報等に数多く記載されているが、一般的には感光体上に
静電的潜像を形成し、続いてトナーにより静電的潜像を
顕像、印刷紙にトナーを転写した後、加熱、加圧、ある
いは溶剤により定着して印刷物を得ている。[Prior Art] Conventionally, as an electrophotographic method, US Pat.
No. 297691, U.S. Patent No. 2874063, Japanese Patent Publication No. 42-23910, Japanese Patent Publication No. 43-24748, etc., but in general, an electrostatic latent image is formed on a photoreceptor, Subsequently, the electrostatic latent image is developed with toner, the toner is transferred to printing paper, and then fixed by heating, pressure, or a solvent to obtain a printed matter.
【0003】種々提案されている定着方法の中で圧力に
よる定着方法は、省エネルギー、無公害、火災に対する
安全性、装置の電源を入れてから待ち時間無く印刷が行
えるなど利点が多く、米国特許第3269626号、特
公昭46−15876号公報等が提案されている。Among the various fixing methods that have been proposed, the pressure fixing method has many advantages such as energy saving, no pollution, safety against fire, and the ability to print without any waiting time after the device is turned on. No. 3269626, Japanese Patent Publication No. 46-15876, etc. have been proposed.
【0004】さらに、圧力定着法に使用するトナーは、
例えば特公昭44−9880号公報には脂肪族成分と熱
可塑性樹脂からなる圧力定着用トナー、特開昭48−7
5033号公報には粘り強い重合体と軟質重合体のブロ
ック重合体からなるトナー、特公昭49−1588号公
報、特公昭51−35867号公報、特公昭54−81
04号公報、特公昭59−1190号公報などの明細書
には内核に軟質物質を含んだマイクロカプセル型の圧力
定着用トナーが記載されている。Furthermore, the toner used in the pressure fixing method is
For example, Japanese Patent Publication No. 44-9880 discloses a pressure fixing toner comprising an aliphatic component and a thermoplastic resin;
Japanese Patent Publication No. 5033 describes toners made of block polymers of a tenacious polymer and a soft polymer, Japanese Patent Publications No. 1588-1988, Japanese Patent Publication No. 35867-1987, and Japanese Patent Publication No. 54-81.
Specifications such as Japanese Patent Publication No. 04 and Japanese Patent Publication No. 59-1190 describe microcapsule-type pressure fixing toners containing a soft material in the inner core.
【0005】[0005]
【発明が解決しようとする課題】しかし、軟質の結着成
分から構成されている特公昭44−9880号公報およ
び特開昭48−75033号公報記載の圧力定着用トナ
ーは、圧力定着は可能であるが、組成物が柔らかいため
に加圧定着装置や現像装置、感光体へのオフセットを起
こし易く、またトナー同士も粘着して凝集やケーキ化を
起こし易い問題点がある。[Problems to be Solved by the Invention] However, the pressure fixing toners described in Japanese Patent Publication No. 44-9880 and Japanese Patent Application Laid-Open No. 48-75033, which are composed of a soft binding component, are not capable of pressure fixing. However, since the composition is soft, it tends to cause offset to the pressure fixing device, developing device, and photoreceptor, and the toners also tend to stick to each other, causing aggregation and caking.
【0006】この問題点を解決するために、特公昭49
−1588号公報、特公昭51−35867号公報、特
公昭54−8104号公報、特公昭59−1190公報
に軟質の結着成分からなるトナーを硬質の樹脂被覆層で
覆ったマイクロカプセルトナーが提案されている。硬質
の樹脂被覆層で軟質のトナ−を覆うことにより、組成物
の柔らかさに起因する粘着性が減少し、現像装置や感光
体へのオフセット、トナー同士の凝集やケーキ化を減ら
すことができる。[0006] In order to solve this problem,
Microcapsule toner in which a toner made of a soft binding component is covered with a hard resin coating layer is proposed in Japanese Patent Publication No. 1588, Japanese Patent Publication No. 51-35867, Japanese Patent Publication No. 54-8104, and Japanese Patent Publication No. 59-1190. has been done. By covering the soft toner with a hard resin coating layer, the tackiness caused by the softness of the composition is reduced, and offset to the developing device and photoreceptor, as well as aggregation and caking of toner particles, can be reduced. .
【0007】マイクロカプセル型の圧力定着用トナーを
使用して均一で良好な定着像を得るためには、加圧時の
トナーの割れ方を一定にすることが望ましく、樹脂被覆
層の膜厚を均一にすることが必要である。また、定着時
の印加圧力を低くするためには、トナー表面の樹脂被覆
層を薄くする必要があるが、樹脂被覆層が斑に付着して
いたり、極端に薄い箇所があると、そこを起点としてオ
フセットや凝集が始まり、トナーの安定性を低下させる
。このため樹脂被覆層は、薄く、かつ均一な厚みが必要
となる。In order to obtain a uniform and good fixed image using a microcapsule type toner for pressure fixing, it is desirable that the toner cracks during pressurization be constant, and the thickness of the resin coating layer should be adjusted. It is necessary to make it uniform. In addition, in order to lower the pressure applied during fixing, it is necessary to make the resin coating layer on the toner surface thinner, but if the resin coating layer adheres to spots or has extremely thin spots, the resin coating layer may become a starting point. Offset and agglomeration begin as a result, reducing toner stability. Therefore, the resin coating layer needs to be thin and uniform in thickness.
【0008】しかし、前記公報の明細書に記載されてい
る、スプレードライ法、相分離法、界面重合法等の従来
のマイクロカプセル作成方法は、樹脂被覆層の付着量制
御が難しく、薄く均一な樹脂被覆層が得られにくい。そ
のため斑や極端に薄い箇所がない樹脂被覆層を得るため
には、膜厚を厚くしなければならず、定着には高い圧力
が必要になる。また、樹脂被覆層の膜厚が不均一なため
、定着画像には定着時の圧力ムラによるボイド等の欠陥
が生じ易く、画像品質が低下するという問題点がある。However, conventional microcapsule production methods such as spray drying, phase separation, and interfacial polymerization described in the specification of the above-mentioned publication have difficulty controlling the amount of deposited resin coating layer, and do not produce thin and uniform microcapsules. It is difficult to obtain a resin coating layer. Therefore, in order to obtain a resin coating layer without spots or extremely thin spots, the film must be thick, and high pressure is required for fixing. Further, since the thickness of the resin coating layer is non-uniform, defects such as voids are likely to occur in the fixed image due to uneven pressure during fixing, resulting in a problem in that the image quality is degraded.
【0009】さらに、トナーと被覆層の材料の組み合わ
せが限定され、材料の選択幅が狭い、トナーと樹脂被覆
層の密着性が低いために、わずかな衝撃でも被覆層が剥
離しやすくトナーの寿命が短いという問題点も挙げられ
ている。Furthermore, the combinations of materials for the toner and the coating layer are limited, the selection range of materials is narrow, and the adhesion between the toner and the resin coating layer is low, so the coating layer is likely to peel off even with the slightest impact, shortening the life of the toner. Another problem is that the length is too short.
【0010】従って本発明は、トナーオフセットやトナ
ー凝集が生じない、トナー寿命が長い、さらに均一で良
好な定着像が得られる圧力定着用トナーの製造方法を提
供する事を目的としている。SUMMARY OF THE INVENTION Accordingly, an object of the present invention is to provide a method for producing a toner for pressure fixing, which does not cause toner offset or aggregation, has a long toner life, and provides a uniform and good fixed image.
【0011】[0011]
【課題を解決するための手段】本発明の圧力定着用トナ
ーの製造方法は、少なくとも結着成分と着色材からなる
トナー内核を作成する工程と、トナー内核表面に粒子径
が0.05〜0.5μmの範囲、かつ尖度が10000
以上の極めて狭い粒子径分布を有する樹脂粒子を一層付
着する工程と、前記工程により得られる樹脂粒子付着ト
ナー内核を溶剤に接触し、トナー内核表面に樹脂被覆層
を形成してマイクロカプセル化する工程からなることを
特徴とする。[Means for Solving the Problems] The method for producing a toner for pressure fixing according to the present invention includes a step of creating a toner inner core consisting of at least a binding component and a coloring material, and a particle size of 0.05 to 0 on the surface of the toner inner core. .5μm range and kurtosis 10000
A step of attaching a layer of resin particles having an extremely narrow particle size distribution as described above, and a step of contacting the resin particle-attached toner inner core obtained in the above step with a solvent to form a resin coating layer on the surface of the toner inner core to microcapsule it. It is characterized by consisting of.
【0012】0012
【作用】本発明の圧力定着用トナーの製造方法における
トナー内核への樹脂粒子の付着は、メカノケミカル法、
樹脂粒子と共存下でのスプレードライ法、溶媒分散下で
のヘテロ凝集法等により行うため、一層付着が均一に出
来る。また、樹脂粒子層から樹脂被覆層の形成は、樹脂
粒子を溶剤で溶解してトナー内核表面に樹脂溶液層を形
成し、さらに溶液層から溶剤を乾燥除去して行っている
。このため、形成する樹脂被覆層の厚みは、樹脂粒子の
粒子径の調整により制御可能であり、さらに用いる樹脂
粒子の粒子径分布が極めて狭いために樹脂被覆層の膜厚
ムラを極めて小さくするこができる。この結果、薄く、
かつ均一な厚みの樹脂層を有する圧力定着用マイクロカ
プセルトナーを作成することができ、トナーオフセット
やトナー凝集が生じない、トナー寿命が長い、さらに均
一で良好な定着像が得られる圧力定着用トナーの製造方
法を提供する事が可能になる。[Function] In the method for producing a toner for pressure fixing of the present invention, resin particles can be attached to the toner inner core by a mechanochemical method,
Since it is carried out by a spray drying method in the coexistence of resin particles, a heteroaggregation method in a solvent dispersion, etc., the adhesion can be made more uniform. The resin coating layer is formed from the resin particle layer by dissolving the resin particles with a solvent to form a resin solution layer on the surface of the toner inner core, and then drying and removing the solvent from the solution layer. Therefore, the thickness of the resin coating layer to be formed can be controlled by adjusting the particle size of the resin particles, and since the particle size distribution of the resin particles used is extremely narrow, it is possible to extremely reduce unevenness in the thickness of the resin coating layer. Can be done. As a result, thin
A toner for pressure fixing that can create a microcapsule toner for pressure fixing that has a resin layer with a uniform thickness, does not cause toner offset or aggregation, has a long toner life, and provides a uniform and good fixed image. It becomes possible to provide a manufacturing method for
【0013】以下、実施例により本発明を詳細に説明す
る。The present invention will be explained in detail below with reference to Examples.
【0014】[0014]
【実施例】図1に本発明による圧力定着用トナーの製造
方法を実施するためのフローチャートの一例を示す。DESCRIPTION OF THE PREFERRED EMBODIMENTS FIG. 1 shows an example of a flowchart for carrying out the method for producing a pressure fixing toner according to the present invention.
【0015】結着成分1は、ワックス、樹脂類が用いら
れ、キャンデリラワックス、カルナバワックス等の植物
系ワックス、みつろう、ラノリン等の動物系ワックス、
モンタンワックス等の鉱物系ワックス、パラフィンワッ
クス、マイクロクリスタリンワックス等の石油系ワック
ス、ポリエチレンワックス、フィッシャートロプスワッ
クス等の合成炭化水素系ワックス、モンタンワックス誘
導体、パラフィンワックス誘導体などの変性ワックス、
硬化ひまし油、硬化ひまし油誘導体等の水素化ワックス
、脂肪酸、酸アミド、エステル、ケトン等の合成ワック
ス類、およびポリアクリレート誘導体、ポリメタクリレ
ート誘導体、ポリスチレン誘導体、ブチラール樹脂、ポ
リエステル樹脂、セルロース樹脂、ポリエチレン樹脂、
ポリプロピレン樹脂、酢酸ビニル樹脂、さらにこれらの
共重合体の熱可塑性樹脂が使用され、これらが単独また
は複数混合されて使用される。As the binding component 1, waxes and resins are used, including vegetable waxes such as candelilla wax and carnauba wax, animal waxes such as beeswax and lanolin,
Mineral waxes such as montan wax, petroleum waxes such as paraffin wax and microcrystalline wax, synthetic hydrocarbon waxes such as polyethylene wax and Fischer-Trops wax, modified waxes such as montan wax derivatives and paraffin wax derivatives,
Hydrogenated waxes such as hydrogenated castor oil and hydrogenated castor oil derivatives, synthetic waxes such as fatty acids, acid amides, esters, and ketones, and polyacrylate derivatives, polymethacrylate derivatives, polystyrene derivatives, butyral resins, polyester resins, cellulose resins, polyethylene resins,
Polypropylene resin, vinyl acetate resin, and thermoplastic resins such as copolymers thereof are used, and these may be used alone or in combination.
【0016】着色材2は、カーボンブラック類、アゾ系
、アズレニウム系、アントラキノン系、インジゴ系、チ
オインジゴ系、キナクリドン系、多環キノン系、シアニ
ン系、ジオキサジン系、スクアリリウム系、スチルベン
系、ピリリウム系、フタロシアニン系、ナフタロシアニ
ン系、ピリジノポルフィラジン系、ペリレン系、ベンジ
ジン系などの染顔料が使用される。Colorant 2 includes carbon blacks, azo, azulenium, anthraquinone, indigo, thioindigo, quinacridone, polycyclic quinone, cyanine, dioxazine, squarylium, stilbene, pyrylium, Phthalocyanine-based, naphthalocyanine-based, pyridinoporphyrazine-based, perylene-based, benzidine-based dyes and pigments are used.
【0017】樹脂粒子3は、ポリアクリレート誘導体、
ポリメタクリレート誘導体、ポリスチレン誘導体、ポリ
エチレン樹脂、ポリプロピレン樹脂、酢酸ビニル樹脂、
およびこれらの共重合体からなり、乳化重合、懸濁重合
、分散重合等の重合法で作成される。また、ポリエステ
ル樹脂、セルロース樹脂、ブチラール樹脂等の微粉砕ま
たは噴霧乾燥により作成した樹脂粒子を使用することも
可能である。粒子径は、0.05〜0.5μmの範囲が
好ましく、トナーの外周に形成する樹脂被覆層の膜厚に
応じて粒子径が調整される。[0017] The resin particles 3 are made of a polyacrylate derivative,
Polymethacrylate derivatives, polystyrene derivatives, polyethylene resins, polypropylene resins, vinyl acetate resins,
and a copolymer thereof, and is produced by polymerization methods such as emulsion polymerization, suspension polymerization, and dispersion polymerization. It is also possible to use resin particles prepared by finely pulverizing or spray drying polyester resin, cellulose resin, butyral resin, etc. The particle size is preferably in the range of 0.05 to 0.5 μm, and is adjusted depending on the thickness of the resin coating layer formed on the outer periphery of the toner.
【0018】粒子径分布は、[0018] The particle size distribution is
【0019】[0019]
【数1】Σ(di4・ηi)/{Σ(di2・ηi)}
4di:平均粒子径との差
ηi:頻度比率
で定義される尖度が10000以上のものが望ましい。[Math. 1] Σ(di4・ηi)/{Σ(di2・ηi)}
4di: difference from average particle diameter ηi: kurtosis defined by frequency ratio is preferably 10,000 or more.
【0020】溶剤4は、樹脂粒子3を溶解してトナー内
核表面に樹脂被覆層を形成するために用いられ、ジクロ
ロメタン、クロロホルム、四塩化炭素、ジクロロエタン
、クロロベンゼン等のハロゲン化炭化水素類、メタノー
ル、メチルセルソルブ、ベンジルアルコール等のアルコ
ール類、ジオキサン、テトラヒドロフラン、ベンジルエ
ーテル等のエーテル類等、酢酸エチル、酢酸ブチル等の
エステル類、フルフラール、アセトン、メチルエチルケ
トン、シクロヘキサノン等のケトン類、ベンゼン、トル
エン、キシレン等の芳香族類、ニトロベンゼン、アセト
ニトリル、ジエチルアミン、アニリン、ジメチルホルム
アミド、ピロリドン等の窒素化合物の中から、樹脂粒子
3を構成する樹脂の種類により適宜選択される。樹脂粒
子3と溶剤4の組み合わせは、N.M.Bikales
,Encyclopediaof Polymer
Science and Technology
,Vol.12,P600〜625 (1970)記
載に従って、溶解度パラメーターと溶剤の水素結合力を
指標に選択できる。The solvent 4 is used to dissolve the resin particles 3 and form a resin coating layer on the surface of the inner core of the toner, and includes halogenated hydrocarbons such as dichloromethane, chloroform, carbon tetrachloride, dichloroethane, and chlorobenzene, methanol, Alcohols such as methyl cellosolve and benzyl alcohol, ethers such as dioxane, tetrahydrofuran and benzyl ether, esters such as ethyl acetate and butyl acetate, ketones such as furfural, acetone, methyl ethyl ketone and cyclohexanone, benzene, toluene and xylene. and nitrogen compounds such as nitrobenzene, acetonitrile, diethylamine, aniline, dimethylformamide, and pyrrolidone, depending on the type of resin constituting the resin particles 3. The combination of resin particles 3 and solvent 4 is N. M. Bikales
, Encyclopedia of Polymer
Science and Technology
, Vol. 12, P600-625 (1970), it can be selected using the solubility parameter and the hydrogen bonding strength of the solvent as indicators.
【0021】混練5は、連続式ではスクリュー押し出し
機、バッチ式ではバンバリーミキサー等、湿式混練では
ホモジナイザー、コロイドミル、ボールミル等が使用さ
れる。微粉砕6は、ジェットミル、カッターミル、オン
グミル、ボールミル等により粒径5〜30μmの微粉体
に粉砕され、トナー内核7が得られる。For kneading 5, a screw extruder is used for continuous kneading, a Banbury mixer or the like is used for batch kneading, and a homogenizer, colloid mill, ball mill, etc. is used for wet kneading. The finely pulverized powder 6 is pulverized into a fine powder having a particle size of 5 to 30 μm using a jet mill, a cutter mill, an angular mill, a ball mill, or the like, and the toner inner core 7 is obtained.
【0022】電子写真式現像方法に磁性現像法を用いる
場合は、トナー内核7にはフェライト、マグネタイト、
鉄、クロム、ニッケル等の磁性材料からなる磁性粉が添
加される。また、着色材2、磁性粉を結着成分1に分散
するためにアニオン性界面活性剤類、カチオン性界面活
性剤類、ノニオン性界面活性剤類、ポリアクリル酸塩誘
導体、ポリメタクリル酸塩誘導体、無水マレイン酸共重
合体等のポリカルボン酸塩類、ソルスパース系超分散剤
などの分散剤を添加することも可能である。When a magnetic development method is used in the electrophotographic development method, the toner inner core 7 contains ferrite, magnetite,
Magnetic powder made of magnetic materials such as iron, chromium, and nickel is added. In addition, anionic surfactants, cationic surfactants, nonionic surfactants, polyacrylate derivatives, polymethacrylate derivatives are used to disperse colorant 2 and magnetic powder in binding component 1. It is also possible to add a dispersant such as polycarboxylic acid salts such as , maleic anhydride copolymer, and Solsperse super dispersant.
【0023】続いて、トナー内核7に樹脂粒子3を付着
処理8して樹脂粒子付着トナー内核9が得られる。付着
処理8は、ボールミル、シェーカー、オングミル等を使
用したメカノケミカル法、樹脂粒子と共存下でのスプレ
ードライ法、溶媒分散下でのヘテロ凝集法などが用いら
れる。Subsequently, resin particles 3 are attached to the toner inner core 7 in a process 8 to obtain a resin particle-attached toner inner core 9. For the adhesion treatment 8, a mechanochemical method using a ball mill, a shaker, an ong mill, etc., a spray drying method in coexistence with resin particles, a heteroaggregation method under solvent dispersion, etc. are used.
【0024】樹脂粒子付着トナー内核9は、溶剤4によ
り被膜処理10して圧力定着用トナー11が作成される
。The toner inner core 9 to which the resin particles are attached is subjected to a coating treatment 10 with a solvent 4 to produce a toner 11 for pressure fixing.
【0025】被膜処理10は、溶解速度が遅い樹脂粒子
/溶剤系では樹脂粒子付着トナー内核9を溶剤に分散し
、濾過乾燥もしくはスプレードライ法により作成する。
溶解速度が早い系では樹脂粒子付着トナー内核9の溶剤
蒸気処理、溶剤ミスト処理して被膜化する方法等が上げ
られ、スプレードライヤーやディスパーコート(日清エ
ンジニアリング製)、コートマイザー(フロイント産業
製)等の粉体−液体混合ノズルを有するコーティング装
置により行われる。In the case of a resin particle/solvent system having a slow dissolution rate, the coating treatment 10 is performed by dispersing the toner inner core 9 to which the resin particles are attached in a solvent, and performing filtration drying or spray drying. For systems with a fast dissolution rate, there are methods in which the toner inner core 9 with resin particles is treated with solvent vapor or solvent mist to form a film, such as spray dryer, Disper Coat (manufactured by Nisshin Engineering), Coat Mizer (manufactured by Freund Sangyo), etc. This is carried out using a coating device having a powder-liquid mixing nozzle such as .
【0026】また、電子写真法による現像を安定化し、
トナー流動性を改善するために荷電制御剤、流動性向上
剤等の機能性付与剤を添加、外添する事も可能である。
荷電制御剤としては、ニグロシン等の有機金属錯塩類、
アルキルアンモニウム塩類等の有機塩類、高分子カルボ
ン酸類等が用いられ、流動性向上剤としては、酸化チタ
ン、シリカ等の酸化物、窒化物、硫化物、ポリフルオロ
ビニリデン等のフッ素樹脂類の微粉末が用いられる。[0026] It also stabilizes development by electrophotography,
In order to improve toner fluidity, it is also possible to add or externally add functional agents such as charge control agents and fluidity improvers. As charge control agents, organometallic complex salts such as nigrosine,
Organic salts such as alkylammonium salts, polymeric carboxylic acids, etc. are used, and as fluidity improvers, fine powders of oxides such as titanium oxide and silica, nitrides, sulfides, and fluororesins such as polyfluorovinylidene are used. is used.
【0027】本発明を以下の実施例によりさらに詳細に
説明する。The present invention will be explained in more detail by the following examples.
【0028】(実施例1)
結着成分 ポリエチレンワックス
30 g
エチレン−酢酸ビニル
共重合体 27 g
着色材 チャンネルブラック
3 g
磁性粉 マグネタイト
4
0 g上記をバッチ式混練機により混合混練を行い、
ジェットミルにより10〜15μmの微粒子に微粉砕し
てトナー内核を作成した。(Example 1) Binding component polyethylene wax
30g
Ethylene-vinyl acetate copolymer 27 g
Coloring material channel black
3g
magnetic powder magnetite
4
0 g The above was mixed and kneaded using a batch type kneader,
The powder was pulverized into fine particles of 10 to 15 μm using a jet mill to prepare a toner inner core.
【0029】トナー内核全量に対して
樹脂粒子 スチレン−メチルメタクリレ
ート共重合体(粒径0.3μm)
23
gを混合、オングミルにより付着処理を行い、続い
て分級処理によりトナー内核に付着していない樹脂粒子
を除去し、樹脂粒子付着トナー内核を作成した。Based on the total amount of toner core: Resin particles Styrene-methyl methacrylate copolymer (particle size 0.3 μm)
23
g was mixed, subjected to an adhesion treatment using an ong mill, and then subjected to a classification treatment to remove resin particles not attached to the toner inner core, thereby creating a toner inner core with resin particles attached thereto.
【0030】樹脂粒子付着トナー内核を粉体供給ノズル
から吐出しながら、同時に樹脂粒子を溶解する溶剤とし
てトルエンを2流体ノズルからミスト状で吹き付けて被
膜処理を行い、樹脂粒子の溶解と被覆層の形成を行って
圧力定着用トナーを作成した。これを「トナー1」とす
る。While discharging the toner inner core with resin particles from the powder supply nozzle, coating treatment is performed by spraying toluene as a solvent for dissolving the resin particles in a mist form from a two-fluid nozzle, thereby dissolving the resin particles and forming the coating layer. Forming was performed to create a pressure fixing toner. This is referred to as "toner 1".
【0031】(実施例2)
結着成分 マイクロクリスタリンワック
ス 50 g
ブチラール樹脂
47
g 着色材 アセチレンブラック
3
g上記をバッチ式混練機により混練を行い、ジェッ
トミルにより10〜15μmの微粒子に微粉砕してトナ
ー内核を作成した。(Example 2) Binding component Microcrystalline wax 50 g
butyral resin
47
G Colorant Acetylene black
3
g The above mixture was kneaded using a batch type kneader and pulverized into fine particles of 10 to 15 μm using a jet mill to prepare a toner inner core.
【0032】トナー内核全量に対して
樹脂粒子 スチレン−ブチルメタクリレ
ート共重合体(粒径0.4μm)
36
gを混合、ボールミルにより付着処理を行い、続い
て分級処理によりトナー内核に未付着の樹脂粒子を除去
して樹脂粒子付着トナー内核を作成した。Based on the total amount of toner core: Resin particles Styrene-butyl methacrylate copolymer (particle size 0.4 μm)
36
g was mixed, an adhesion treatment was performed using a ball mill, and then resin particles not attached to the toner inner core were removed by a classification treatment to create a toner inner core with resin particles attached.
【0033】樹脂粒子付着トナー内核を、粉体−液体混
合ノズルに供給しながら樹脂粒子を溶解する溶剤として
メチルエチルケトンを供給して被膜処理を行い、圧力定
着用トナーを作成した。これを「トナ−2」とする。The inner core of the toner with resin particles attached thereto was supplied to a powder-liquid mixing nozzle, and methyl ethyl ketone was supplied as a solvent for dissolving the resin particles to perform a coating treatment, thereby producing a toner for pressure fixing. This will be referred to as "toner 2".
【0034】(実施例3)
結着成分 パラフィンワックス
48 g
エチレン−無水マレ
イン酸共重合体 47 g
着色材 フタロシアニンブルー
5 g上記
をバッチ式混練機により混練を行い、ジェットミルによ
り10〜15μmの微粒子に微粉砕してトナー内核を作
成した。(Example 3) Binding component paraffin wax
48g
Ethylene-maleic anhydride copolymer 47 g
Coloring material Phthalocyanine blue
5 g of the above was kneaded using a batch type kneader and pulverized into fine particles of 10 to 15 μm using a jet mill to prepare a toner inner core.
【0035】トナー内核全量に対して
樹脂粒子 メチルメタクリレート−ブチ
ルメタクリレート共重合体
(粒径0.1μm)
10 gを混合、メカノフー
ジョンにより付着処理を行い、続いて分級処理によりト
ナー内核に未付着の樹脂粒子を除去して樹脂粒子付着ト
ナー内核を作成した。Resin particles Methyl methacrylate-butyl methacrylate copolymer based on the total amount of toner core
(particle size 0.1μm)
10 g were mixed and subjected to adhesion treatment using mechanofusion, followed by classification treatment to remove resin particles not attached to the toner inner core to create a resin particle-attached toner inner core.
【0036】樹脂粒子付着トナー内核を、樹脂粒子が溶
解するメチルエチルケトンと溶解しないメタノールを混
合して溶解速度を遅くした溶剤に分散し、スプレードラ
イ法により樹脂粒子の溶解と被覆層の形成を行って圧力
定着用トナーを作成した。これを「トナ−3」とする。The inner core of the toner with resin particles attached thereto is dispersed in a solvent in which the dissolution rate is slowed by mixing methyl ethyl ketone, which dissolves the resin particles, and methanol, which does not dissolve the resin particles, and the resin particles are dissolved and a coating layer is formed by a spray drying method. A toner for pressure fixing was created. This will be referred to as "toner 3".
【0037】(比較例1)実施例1に従って作成したト
ナー内核全量を、スチレン−メチルメタクリレート共重
合体の3%トルエン溶液に分散し、スプレードライ法を
行って樹脂被覆層を形成して圧力定着用トナーを作成し
た。これを「トナー4」とする。(Comparative Example 1) The entire amount of the inner core of the toner prepared according to Example 1 was dispersed in a 3% toluene solution of styrene-methyl methacrylate copolymer, and a resin coating layer was formed by spray drying, followed by pressure fixing. I created a toner for. This will be referred to as "toner 4."
【0038】トナー1から4について、断面の透過電子
顕微鏡観察を行い樹脂被覆層の平均厚みを求めた結果を
表1に示す。For Toners 1 to 4, cross sections were observed with a transmission electron microscope to determine the average thickness of the resin coating layer. Table 1 shows the results.
【0039】[0039]
【表1】[Table 1]
【0040】本発明のトナー1、2、3は、付着した樹
脂粒子の粒子径に依存した厚みの樹脂被覆層が、トナー
全周に渡って均一に形成されていた。ただし、樹脂粒子
の粒子径から計算される厚みより若干薄い傾向が認めら
れた。これに対して比較例1のトナー4では、0.02
μm以下の厚みであり、膜厚も不均一であった。In Toners 1, 2, and 3 of the present invention, a resin coating layer having a thickness depending on the particle diameter of the attached resin particles was uniformly formed over the entire circumference of the toner. However, it was observed that the thickness tended to be slightly thinner than that calculated from the particle size of the resin particles. On the other hand, in Toner 4 of Comparative Example 1, 0.02
The thickness was less than μm, and the film thickness was also non-uniform.
【0041】次に、トナー1から4を電子写真式の印刷
装置により印刷試験を行い、現像定着性、凝集性の比較
した結果を表2に示す。現像定着性は、10000枚印
刷時の印刷紙上の白抜け、濃度ムラ等の有無から判断し
た。凝集性は、10時間印刷せずに印刷装置を作動させ
、作動前後のトナーの平均粒子径と安息角の変化から判
断した。Next, toners 1 to 4 were subjected to a printing test using an electrophotographic printing device, and Table 2 shows the results of a comparison of development and fixing properties and cohesive properties. The development and fixing properties were judged from the presence or absence of white spots, density unevenness, etc. on the printed paper when 10,000 sheets were printed. Cohesiveness was determined by operating the printing apparatus for 10 hours without printing, and from changes in the average particle diameter and angle of repose of the toner before and after operation.
【0042】[0042]
【表2】[Table 2]
【0043】表2に示す様に、本発明のトナー1、2、
3は、現像定着時に白抜け等の印刷ムラがなく、濃度が
均一で良好な印刷物が得られた。これに対して比較例の
トナー4の印刷物には、白スジや白点が認められ、凝集
トナーの発生や定着不良が生じている。さらに黒ベタ部
分の濃度ムラも顕著であった。As shown in Table 2, toners 1, 2, and
In Sample No. 3, there was no printing unevenness such as white spots during development and fixation, and a good printed matter with uniform density was obtained. On the other hand, in the printed matter of Comparative Example Toner 4, white streaks and white spots were observed, and the occurrence of agglomerated toner and poor fixing occurred. Furthermore, density unevenness in solid black areas was also noticeable.
【0044】また、凝集性についてもトナー1、2、3
では、10時間の印刷装置の作動前後でのトナーの平均
粒子径と安息角の変化が少なく、凝集性は認められなか
った。これに対して比較例のトナー4は、平均粒子径が
拡大し、安息角が上昇しており、トナーが強く凝集して
いる。[0044] Regarding the cohesive property, toners 1, 2, and 3
In this case, there was little change in the average particle diameter and angle of repose of the toner before and after the operation of the printing device for 10 hours, and no cohesiveness was observed. On the other hand, in Toner 4 of Comparative Example, the average particle diameter is increased, the angle of repose is increased, and the toner is strongly aggregated.
【0045】[0045]
【発明の効果】以上述べたように本発明によれば、トナ
ー画像を有する印刷紙に圧力を加えてトナー画像の定着
を行う方法に使用する圧力定着用トナーの製造方法にお
いて、少なくとも結着成分と着色材からなるトナー内核
を作成する工程と、トナー内核表面に粒子径が0.05
〜0.5μmの範囲、かつ尖度が10000以上の極め
て狭い粒子径分布を有する樹脂粒子を一層付着する工程
と、前記工程により得られる樹脂粒子付着トナー内核を
溶剤に接触し、トナー内核表面に樹脂被覆層を形成して
マイクロカプセル化する工程からなることにより、樹脂
被覆層を薄く、かつ均一な厚みで形成することが可能に
なり、トナーオフセットやトナー凝集が生じない、トナ
ー寿命が長い、さらに均一で良好な定着像が得られる圧
力定着用トナーの製造方法を提供する事が可能になった
。As described above, according to the present invention, in a method for producing a pressure fixing toner used in a method of fixing a toner image by applying pressure to printing paper having a toner image, at least the binding component and a step of creating a toner inner core consisting of a coloring material, and a step of creating a toner inner core consisting of a colorant and a particle size of 0.05 on the surface of the toner inner core.
A step of further adhering resin particles having an extremely narrow particle size distribution in the range of ~0.5 μm and a kurtosis of 10,000 or more, and contacting the resin particle-attached toner inner core obtained by the above step with a solvent to coat the surface of the toner inner core. By forming a resin coating layer and microcapsulating it, it is possible to form a thin and uniform resin coating layer, which eliminates toner offset and aggregation, and provides long toner life. Furthermore, it has become possible to provide a method for producing a pressure fixing toner that provides a uniform and good fixed image.
【図1】本発明による圧力定着用トナーの製造方法を実
施するためのフローチャートの一例を示す図。FIG. 1 is a diagram showing an example of a flowchart for carrying out a method for manufacturing a pressure fixing toner according to the present invention.
1 結着成分 2 着色材 3 樹脂粒子 4 溶剤 5 混練 6 微粉砕 7 トナー内核 8 付着処理 9 樹脂粒子付着トナー内核 10 被膜処理 11 圧力定着用トナー 1. Binding component 2 Coloring material 3 Resin particles 4 Solvent 5 Kneading 6 Fine grinding 7 Toner inner core 8 Adhesion treatment 9 Toner inner core with resin particles attached 10 Film treatment 11 Pressure fixing toner
Claims (1)
えてトナー画像の定着を行う方法に使用する圧力定着用
トナーの製造方法において、少なくとも結着成分と着色
材からなるトナー内核を作成する工程と、トナー内核表
面に粒子径が0.05〜0.5μmの範囲、かつ尖度が
10000以上の極めて狭い粒子径分布を有する樹脂粒
子を一層付着する工程と、前記工程により得られる樹脂
粒子付着トナー内核を溶剤に接触し、トナー内核表面に
樹脂被覆層を形成してマイクロカプセル化する工程から
なることを特徴とする圧力定着用トナーの製造方法。1. A method for producing a pressure fixing toner used in a method of fixing a toner image by applying pressure to printing paper having a toner image, the step of creating a toner inner core consisting of at least a binding component and a coloring material. , a step of further adhering resin particles having an extremely narrow particle size distribution with a particle size in the range of 0.05 to 0.5 μm and a kurtosis of 10,000 or more on the surface of the inner core of the toner; and a step of adhering the resin particles obtained by the above step. 1. A method for producing a toner for pressure fixing, comprising the steps of contacting a toner inner core with a solvent, forming a resin coating layer on the surface of the toner inner core, and microcapsulating the toner core.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP3105728A JPH04333854A (en) | 1991-05-10 | 1991-05-10 | Production of toner for pressure fixing |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP3105728A JPH04333854A (en) | 1991-05-10 | 1991-05-10 | Production of toner for pressure fixing |
Publications (1)
Publication Number | Publication Date |
---|---|
JPH04333854A true JPH04333854A (en) | 1992-11-20 |
Family
ID=14415362
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP3105728A Pending JPH04333854A (en) | 1991-05-10 | 1991-05-10 | Production of toner for pressure fixing |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH04333854A (en) |
-
1991
- 1991-05-10 JP JP3105728A patent/JPH04333854A/en active Pending
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