JPH06148926A - Method for forming image - Google Patents
Method for forming imageInfo
- Publication number
- JPH06148926A JPH06148926A JP4322266A JP32226692A JPH06148926A JP H06148926 A JPH06148926 A JP H06148926A JP 4322266 A JP4322266 A JP 4322266A JP 32226692 A JP32226692 A JP 32226692A JP H06148926 A JPH06148926 A JP H06148926A
- Authority
- JP
- Japan
- Prior art keywords
- toner
- image forming
- developer
- image
- forming method
- 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.)
- Withdrawn
Links
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- 238000004140 cleaning Methods 0.000 claims abstract description 37
- 238000012546 transfer Methods 0.000 claims abstract description 15
- 239000000178 monomer Substances 0.000 claims description 28
- 239000011347 resin Substances 0.000 claims description 19
- 229920005989 resin Polymers 0.000 claims description 19
- YBJHBAHKTGYVGT-ZKWXMUAHSA-N (+)-Biotin Chemical compound N1C(=O)N[C@@H]2[C@H](CCCCC(=O)O)SC[C@@H]21 YBJHBAHKTGYVGT-ZKWXMUAHSA-N 0.000 claims description 16
- FEPMHVLSLDOMQC-UHFFFAOYSA-N virginiamycin-S1 Natural products CC1OC(=O)C(C=2C=CC=CC=2)NC(=O)C2CC(=O)CCN2C(=O)C(CC=2C=CC=CC=2)N(C)C(=O)C2CCCN2C(=O)C(CC)NC(=O)C1NC(=O)C1=NC=CC=C1O FEPMHVLSLDOMQC-UHFFFAOYSA-N 0.000 claims description 16
- 239000011164 primary particle Substances 0.000 claims description 13
- 239000000203 mixture Substances 0.000 claims description 12
- 238000003825 pressing Methods 0.000 claims description 7
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- 230000005684 electric field Effects 0.000 claims description 4
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- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 2
- SJIXRGNQPBQWMK-UHFFFAOYSA-N 2-(diethylamino)ethyl 2-methylprop-2-enoate Chemical compound CCN(CC)CCOC(=O)C(C)=C SJIXRGNQPBQWMK-UHFFFAOYSA-N 0.000 description 2
- JKNCOURZONDCGV-UHFFFAOYSA-N 2-(dimethylamino)ethyl 2-methylprop-2-enoate Chemical compound CN(C)CCOC(=O)C(C)=C JKNCOURZONDCGV-UHFFFAOYSA-N 0.000 description 2
- SOGAXMICEFXMKE-UHFFFAOYSA-N Butylmethacrylate Chemical compound CCCCOC(=O)C(C)=C SOGAXMICEFXMKE-UHFFFAOYSA-N 0.000 description 2
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- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 2
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 2
- BAPJBEWLBFYGME-UHFFFAOYSA-N Methyl acrylate Chemical compound COC(=O)C=C BAPJBEWLBFYGME-UHFFFAOYSA-N 0.000 description 2
- XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 description 2
- ADCOVFLJGNWWNZ-UHFFFAOYSA-N antimony trioxide Chemical compound O=[Sb]O[Sb]=O ADCOVFLJGNWWNZ-UHFFFAOYSA-N 0.000 description 2
- CQEYYJKEWSMYFG-UHFFFAOYSA-N butyl acrylate Chemical compound CCCCOC(=O)C=C CQEYYJKEWSMYFG-UHFFFAOYSA-N 0.000 description 2
- 239000006229 carbon black Substances 0.000 description 2
- 239000003086 colorant Substances 0.000 description 2
- 238000007334 copolymerization reaction Methods 0.000 description 2
- GMSCBRSQMRDRCD-UHFFFAOYSA-N dodecyl 2-methylprop-2-enoate Chemical compound CCCCCCCCCCCCOC(=O)C(C)=C GMSCBRSQMRDRCD-UHFFFAOYSA-N 0.000 description 2
- 239000000975 dye Substances 0.000 description 2
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- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 2
- 230000002209 hydrophobic effect Effects 0.000 description 2
- 238000005286 illumination Methods 0.000 description 2
- PBOSTUDLECTMNL-UHFFFAOYSA-N lauryl acrylate Chemical compound CCCCCCCCCCCCOC(=O)C=C PBOSTUDLECTMNL-UHFFFAOYSA-N 0.000 description 2
- 229910052749 magnesium Inorganic materials 0.000 description 2
- 239000011777 magnesium Substances 0.000 description 2
- 238000005259 measurement Methods 0.000 description 2
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- 125000005395 methacrylic acid group Chemical group 0.000 description 2
- 125000002347 octyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 2
- 239000003921 oil Substances 0.000 description 2
- 238000010298 pulverizing process Methods 0.000 description 2
- 150000003242 quaternary ammonium salts Chemical class 0.000 description 2
- 238000000926 separation method Methods 0.000 description 2
- 229920002050 silicone resin Polymers 0.000 description 2
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- 239000004945 silicone rubber Substances 0.000 description 2
- 239000011734 sodium Substances 0.000 description 2
- 229910052708 sodium Inorganic materials 0.000 description 2
- RPACBEVZENYWOL-XFULWGLBSA-M sodium;(2r)-2-[6-(4-chlorophenoxy)hexyl]oxirane-2-carboxylate Chemical compound [Na+].C=1C=C(Cl)C=CC=1OCCCCCC[C@]1(C(=O)[O-])CO1 RPACBEVZENYWOL-XFULWGLBSA-M 0.000 description 2
- 239000007787 solid Substances 0.000 description 2
- 238000012360 testing method Methods 0.000 description 2
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 2
- 229910000859 α-Fe Inorganic materials 0.000 description 2
- DNIAPMSPPWPWGF-GSVOUGTGSA-N (R)-(-)-Propylene glycol Chemical compound C[C@@H](O)CO DNIAPMSPPWPWGF-GSVOUGTGSA-N 0.000 description 1
- IQBLWPLYPNOTJC-FPLPWBNLSA-N (z)-4-(2-ethylhexoxy)-4-oxobut-2-enoic acid Chemical compound CCCCC(CC)COC(=O)\C=C/C(O)=O IQBLWPLYPNOTJC-FPLPWBNLSA-N 0.000 description 1
- WBYWAXJHAXSJNI-VOTSOKGWSA-M .beta-Phenylacrylic acid Natural products [O-]C(=O)\C=C\C1=CC=CC=C1 WBYWAXJHAXSJNI-VOTSOKGWSA-M 0.000 description 1
- BJQFWAQRPATHTR-UHFFFAOYSA-N 1,2-dichloro-4-ethenylbenzene Chemical compound ClC1=CC=C(C=C)C=C1Cl BJQFWAQRPATHTR-UHFFFAOYSA-N 0.000 description 1
- KTZVZZJJVJQZHV-UHFFFAOYSA-N 1-chloro-4-ethenylbenzene Chemical compound ClC1=CC=C(C=C)C=C1 KTZVZZJJVJQZHV-UHFFFAOYSA-N 0.000 description 1
- OEVVKKAVYQFQNV-UHFFFAOYSA-N 1-ethenyl-2,4-dimethylbenzene Chemical compound CC1=CC=C(C=C)C(C)=C1 OEVVKKAVYQFQNV-UHFFFAOYSA-N 0.000 description 1
- NVZWEEGUWXZOKI-UHFFFAOYSA-N 1-ethenyl-2-methylbenzene Chemical compound CC1=CC=CC=C1C=C NVZWEEGUWXZOKI-UHFFFAOYSA-N 0.000 description 1
- JZHGRUMIRATHIU-UHFFFAOYSA-N 1-ethenyl-3-methylbenzene Chemical compound CC1=CC=CC(C=C)=C1 JZHGRUMIRATHIU-UHFFFAOYSA-N 0.000 description 1
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- QEDJMOONZLUIMC-UHFFFAOYSA-N 1-tert-butyl-4-ethenylbenzene Chemical compound CC(C)(C)C1=CC=C(C=C)C=C1 QEDJMOONZLUIMC-UHFFFAOYSA-N 0.000 description 1
- JAHNSTQSQJOJLO-UHFFFAOYSA-N 2-(3-fluorophenyl)-1h-imidazole Chemical compound FC1=CC=CC(C=2NC=CN=2)=C1 JAHNSTQSQJOJLO-UHFFFAOYSA-N 0.000 description 1
- QHVBLSNVXDSMEB-UHFFFAOYSA-N 2-(diethylamino)ethyl prop-2-enoate Chemical compound CCN(CC)CCOC(=O)C=C QHVBLSNVXDSMEB-UHFFFAOYSA-N 0.000 description 1
- DPBJAVGHACCNRL-UHFFFAOYSA-N 2-(dimethylamino)ethyl prop-2-enoate Chemical compound CN(C)CCOC(=O)C=C DPBJAVGHACCNRL-UHFFFAOYSA-N 0.000 description 1
- GOXQRTZXKQZDDN-UHFFFAOYSA-N 2-Ethylhexyl acrylate Chemical compound CCCCC(CC)COC(=O)C=C GOXQRTZXKQZDDN-UHFFFAOYSA-N 0.000 description 1
- WHBAYNMEIXUTJV-UHFFFAOYSA-N 2-chloroethyl prop-2-enoate Chemical compound ClCCOC(=O)C=C WHBAYNMEIXUTJV-UHFFFAOYSA-N 0.000 description 1
- UEHVUTURFVAVOU-UHFFFAOYSA-M 2-ethenyl-1-ethylpyridin-1-ium;chloride Chemical compound [Cl-].CC[N+]1=CC=CC=C1C=C UEHVUTURFVAVOU-UHFFFAOYSA-M 0.000 description 1
- GFHWCDCFJNJRQR-UHFFFAOYSA-M 2-ethenyl-1-methylpyridin-1-ium;chloride Chemical compound [Cl-].C[N+]1=CC=CC=C1C=C GFHWCDCFJNJRQR-UHFFFAOYSA-M 0.000 description 1
- WDQMWEYDKDCEHT-UHFFFAOYSA-N 2-ethylhexyl 2-methylprop-2-enoate Chemical compound CCCCC(CC)COC(=O)C(C)=C WDQMWEYDKDCEHT-UHFFFAOYSA-N 0.000 description 1
- RUMACXVDVNRZJZ-UHFFFAOYSA-N 2-methylpropyl 2-methylprop-2-enoate Chemical compound CC(C)COC(=O)C(C)=C RUMACXVDVNRZJZ-UHFFFAOYSA-N 0.000 description 1
- CFVWNXQPGQOHRJ-UHFFFAOYSA-N 2-methylpropyl prop-2-enoate Chemical compound CC(C)COC(=O)C=C CFVWNXQPGQOHRJ-UHFFFAOYSA-N 0.000 description 1
- KGIGUEBEKRSTEW-UHFFFAOYSA-N 2-vinylpyridine Chemical compound C=CC1=CC=CC=N1 KGIGUEBEKRSTEW-UHFFFAOYSA-N 0.000 description 1
- JLBJTVDPSNHSKJ-UHFFFAOYSA-N 4-Methylstyrene Chemical compound CC1=CC=C(C=C)C=C1 JLBJTVDPSNHSKJ-UHFFFAOYSA-N 0.000 description 1
- JTHZUSWLNCPZLX-UHFFFAOYSA-N 6-fluoro-3-methyl-2h-indazole Chemical compound FC1=CC=C2C(C)=NNC2=C1 JTHZUSWLNCPZLX-UHFFFAOYSA-N 0.000 description 1
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- 229910017518 Cu Zn Inorganic materials 0.000 description 1
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- 229920000297 Rayon Polymers 0.000 description 1
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- 238000005411 Van der Waals force Methods 0.000 description 1
- MCUSVUGKVLTTBA-UHFFFAOYSA-N [3-(dimethylamino)phenyl] prop-2-enoate Chemical compound CN(C)C1=CC=CC(OC(=O)C=C)=C1 MCUSVUGKVLTTBA-UHFFFAOYSA-N 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
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- 150000004996 alkyl benzenes Chemical class 0.000 description 1
- 150000005215 alkyl ethers Chemical class 0.000 description 1
- 125000000217 alkyl group Chemical group 0.000 description 1
- XYLMUPLGERFSHI-UHFFFAOYSA-N alpha-Methylstyrene Chemical compound CC(=C)C1=CC=CC=C1 XYLMUPLGERFSHI-UHFFFAOYSA-N 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
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 1
- 125000003277 amino group Chemical group 0.000 description 1
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- 125000003118 aryl group Chemical group 0.000 description 1
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- 229910002113 barium titanate Inorganic materials 0.000 description 1
- JRPBQTZRNDNNOP-UHFFFAOYSA-N barium titanate Chemical compound [Ba+2].[Ba+2].[O-][Ti]([O-])([O-])[O-] JRPBQTZRNDNNOP-UHFFFAOYSA-N 0.000 description 1
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- TVZPLCNGKSPOJA-UHFFFAOYSA-N copper zinc Chemical compound [Cu].[Zn] TVZPLCNGKSPOJA-UHFFFAOYSA-N 0.000 description 1
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- SUPCQIBBMFXVTL-UHFFFAOYSA-N ethyl 2-methylprop-2-enoate Chemical compound CCOC(=O)C(C)=C SUPCQIBBMFXVTL-UHFFFAOYSA-N 0.000 description 1
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- 125000001153 fluoro group Chemical group F* 0.000 description 1
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- 238000010438 heat treatment Methods 0.000 description 1
- 125000000623 heterocyclic group Chemical group 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 238000010191 image analysis Methods 0.000 description 1
- 229910052742 iron Inorganic materials 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
- MOUPNEIJQCETIW-UHFFFAOYSA-N lead chromate Chemical compound [Pb+2].[O-][Cr]([O-])(=O)=O MOUPNEIJQCETIW-UHFFFAOYSA-N 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 239000000696 magnetic material Substances 0.000 description 1
- 229940002712 malachite green oxalate Drugs 0.000 description 1
- VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 description 1
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- 238000002844 melting Methods 0.000 description 1
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- FQPSGWSUVKBHSU-UHFFFAOYSA-N methacrylamide Chemical compound CC(=C)C(N)=O FQPSGWSUVKBHSU-UHFFFAOYSA-N 0.000 description 1
- WBYWAXJHAXSJNI-UHFFFAOYSA-N methyl p-hydroxycinnamate Natural products OC(=O)C=CC1=CC=CC=C1 WBYWAXJHAXSJNI-UHFFFAOYSA-N 0.000 description 1
- 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
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- YLGYACDQVQQZSW-UHFFFAOYSA-N n,n-dimethylprop-2-enamide Chemical compound CN(C)C(=O)C=C YLGYACDQVQQZSW-UHFFFAOYSA-N 0.000 description 1
- VQGWOOIHSXNRPW-UHFFFAOYSA-N n-butyl-2-methylprop-2-enamide Chemical compound CCCCNC(=O)C(C)=C VQGWOOIHSXNRPW-UHFFFAOYSA-N 0.000 description 1
- YRVUCYWJQFRCOB-UHFFFAOYSA-N n-butylprop-2-enamide Chemical compound CCCCNC(=O)C=C YRVUCYWJQFRCOB-UHFFFAOYSA-N 0.000 description 1
- CNWVYEGPPMQTKA-UHFFFAOYSA-N n-octadecylprop-2-enamide Chemical compound CCCCCCCCCCCCCCCCCCNC(=O)C=C CNWVYEGPPMQTKA-UHFFFAOYSA-N 0.000 description 1
- JCCGSOVTBIJRGP-UHFFFAOYSA-N n-piperidin-1-ylprop-2-enamide Chemical compound C=CC(=O)NN1CCCCC1 JCCGSOVTBIJRGP-UHFFFAOYSA-N 0.000 description 1
- HMZGPNHSPWNGEP-UHFFFAOYSA-N octadecyl 2-methylprop-2-enoate Chemical compound CCCCCCCCCCCCCCCCCCOC(=O)C(C)=C HMZGPNHSPWNGEP-UHFFFAOYSA-N 0.000 description 1
- NZIDBRBFGPQCRY-UHFFFAOYSA-N octyl 2-methylprop-2-enoate Chemical compound CCCCCCCCOC(=O)C(C)=C NZIDBRBFGPQCRY-UHFFFAOYSA-N 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- BMMGVYCKOGBVEV-UHFFFAOYSA-N oxo(oxoceriooxy)cerium Chemical compound [Ce]=O.O=[Ce]=O BMMGVYCKOGBVEV-UHFFFAOYSA-N 0.000 description 1
- RVTZCBVAJQQJTK-UHFFFAOYSA-N oxygen(2-);zirconium(4+) Chemical compound [O-2].[O-2].[Zr+4] RVTZCBVAJQQJTK-UHFFFAOYSA-N 0.000 description 1
- HDBWAWNLGGMZRQ-UHFFFAOYSA-N p-Vinylbiphenyl Chemical compound C1=CC(C=C)=CC=C1C1=CC=CC=C1 HDBWAWNLGGMZRQ-UHFFFAOYSA-N 0.000 description 1
- 239000012188 paraffin wax Substances 0.000 description 1
- PNJWIWWMYCMZRO-UHFFFAOYSA-N pent‐4‐en‐2‐one Natural products CC(=O)CC=C PNJWIWWMYCMZRO-UHFFFAOYSA-N 0.000 description 1
- 230000002093 peripheral effect Effects 0.000 description 1
- QIWKUEJZZCOPFV-UHFFFAOYSA-N phenyl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OC1=CC=CC=C1 QIWKUEJZZCOPFV-UHFFFAOYSA-N 0.000 description 1
- WRAQQYDMVSCOTE-UHFFFAOYSA-N phenyl prop-2-enoate Chemical compound C=CC(=O)OC1=CC=CC=C1 WRAQQYDMVSCOTE-UHFFFAOYSA-N 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 229920000435 poly(dimethylsiloxane) Polymers 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 229920000098 polyolefin Polymers 0.000 description 1
- USHAGKDGDHPEEY-UHFFFAOYSA-L potassium persulfate Chemical compound [K+].[K+].[O-]S(=O)(=O)OOS([O-])(=O)=O USHAGKDGDHPEEY-UHFFFAOYSA-L 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 230000002265 prevention Effects 0.000 description 1
- NHARPDSAXCBDDR-UHFFFAOYSA-N propyl 2-methylprop-2-enoate Chemical compound CCCOC(=O)C(C)=C NHARPDSAXCBDDR-UHFFFAOYSA-N 0.000 description 1
- PNXMTCDJUBJHQJ-UHFFFAOYSA-N propyl prop-2-enoate Chemical compound CCCOC(=O)C=C PNXMTCDJUBJHQJ-UHFFFAOYSA-N 0.000 description 1
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- 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
- 239000004172 quinoline yellow Substances 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 238000005488 sandblasting Methods 0.000 description 1
- 238000007790 scraping Methods 0.000 description 1
- HBMJWWWQQXIZIP-UHFFFAOYSA-N silicon carbide Chemical compound [Si+]#[C-] HBMJWWWQQXIZIP-UHFFFAOYSA-N 0.000 description 1
- 229910010271 silicon carbide Inorganic materials 0.000 description 1
- 238000001694 spray drying Methods 0.000 description 1
- VEALVRVVWBQVSL-UHFFFAOYSA-N strontium titanate Chemical compound [Sr+2].[O-][Ti]([O-])=O VEALVRVVWBQVSL-UHFFFAOYSA-N 0.000 description 1
- 150000003440 styrenes Chemical class 0.000 description 1
- 125000003011 styrenyl group Chemical group [H]\C(*)=C(/[H])C1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 description 1
- 125000000020 sulfo group Chemical group O=S(=O)([*])O[H] 0.000 description 1
- BDHFUVZGWQCTTF-UHFFFAOYSA-M sulfonate Chemical compound [O-]S(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-M 0.000 description 1
- OGIDPMRJRNCKJF-UHFFFAOYSA-N titanium oxide Inorganic materials [Ti]=O OGIDPMRJRNCKJF-UHFFFAOYSA-N 0.000 description 1
- 235000013799 ultramarine blue Nutrition 0.000 description 1
- 229910052720 vanadium Inorganic materials 0.000 description 1
- 229920002554 vinyl polymer Polymers 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
- 239000011701 zinc Substances 0.000 description 1
- 229910052725 zinc Inorganic materials 0.000 description 1
- 239000011787 zinc oxide Substances 0.000 description 1
- 229910001928 zirconium oxide Inorganic materials 0.000 description 1
Landscapes
- Cleaning In Electrography (AREA)
- Developing Agents For Electrophotography (AREA)
Abstract
Description
【0001】[0001]
【産業上の利用分野】本発明は、ブレードを備えたクリ
ーニング装置によって像形成体上の転写残留トナーを除
去する工程を含む画像形成方法に関する。BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to an image forming method including a step of removing transfer residual toner on an image forming body by a cleaning device equipped with a blade.
【0002】[0002]
【従来の技術】従来において、小型かつ低コストで操作
性に優れた装置を用い、解像度の高い高画質の画像を形
成することが可能な技術として、現像剤量規制体の押圧
力を利用して現像剤搬送担持体上に付着した現像剤を薄
層化し、この現像剤の薄層を像形成体に対して非接触で
現像する現像方法が紹介されている(特開昭60−76
766号公報等参照)。特に、この特開昭60−767
66号公報によって開示された多色画像形成方法は、現
像剤が像形成体に非接触で搬送されるため、像形成体上
の画像が現像剤によって乱されることがなく、画像の高
画質化が可能な優れた現像方法である。2. Description of the Related Art Conventionally, as a technique capable of forming a high-quality and high-resolution image by using a device which is small in size, low in cost and excellent in operability, the pressing force of a developer amount regulator is utilized. A developing method has been introduced in which the developer adhered on the developer carrying carrier is thinned and the thin layer of the developer is developed in a non-contact manner with respect to the image forming body (JP-A-60-76).
766, etc.). In particular, this JP-A-60-767
In the multicolor image forming method disclosed in Japanese Patent Publication No. 66, since the developer is conveyed to the image forming body in a non-contact manner, the image on the image forming body is not disturbed by the developer and the image quality is high. It is an excellent development method that can be realized.
【0003】[0003]
【発明が解決しようとする課題】(1)クリーニング不
良 しかして、解像度が高くて鮮鋭性に優れた画像を得るた
めには、小粒径のトナーを用いることが必須の条件であ
る。しかし、小粒径のトナー粒子ほど付着性が大きくな
るため、画像形成プロセスにおける転写工程の終了後、
像形成体上に付着残留している当該トナー粒子をクリー
ニングブレードによって除去しきれないという問題(ク
リーニング不良)が発生し、これが画像乱れ等画像不良
の原因となる。クリーニング不良の問題は、使用するト
ナー粒子の形状が球形に近いほど、また、トナー粒子の
表面に存在する凹凸が少ないほど発生しやすいことが知
られている。これは、球形に近くて凹凸が少ないトナー
粒子ほど、ブレードから擦り抜けやすいからであると考
えられる。一方、このようなクリーニング不良の問題を
解決するため、トナー粒子の歪係数〔(最大長)2 ×π
/(面積×4)×100〕の平均値およびトナー粒子の
凹凸係数〔(周長)2 /(面積×4π)×100〕の平
均値が、それぞれ特定の範囲にあるトナーを用いる技術
が紹介されている(特開昭61−279864号公報参
照)。しかしながら、本発明者らが検討したところ、凹
凸係数の小さいトナー粒子が一定の割合で存在している
場合には、トナー粒子の凹凸係数や歪係数の平均値があ
る程度大きくてもクリーニング不良の発生を十分に防止
できないことが確認された。(1) Poor cleaning However, in order to obtain an image having high resolution and excellent sharpness, it is an essential condition to use a toner having a small particle size. However, the smaller the toner particles, the greater the adhesion, so after the transfer step in the image forming process is completed,
A problem (cleaning failure) occurs in which the toner particles remaining on the image forming body cannot be completely removed by the cleaning blade, which causes image defects such as image distortion. It is known that the problem of cleaning failure is more likely to occur as the shape of the toner particles used is closer to a spherical shape and the unevenness on the surface of the toner particles is smaller. It is considered that this is because toner particles that are closer to a sphere and have less irregularities are more likely to rub through the blade. On the other hand, in order to solve the problem of such cleaning failure, the distortion coefficient of the toner particles [(maximum length) 2 × π
/ (Area x 4) x 100] and the unevenness coefficient of the toner particles [(perimeter) 2 / (area x 4π) x 100] average value are in specific ranges. (See Japanese Patent Laid-Open No. 61-279864). However, as a result of studies by the present inventors, when toner particles having a small unevenness coefficient are present at a constant ratio, cleaning failure occurs even if the average value of the unevenness coefficient and the distortion coefficient of the toner particles is large to some extent. It was confirmed that the above cannot be sufficiently prevented.
【0004】(2)選択現象 上述のように、凹凸度の大きいトナーを用いることはク
リーニング性の向上を図る観点からは好ましい。しかし
ながら、現像剤量規制体の押圧力を利用して現像剤搬送
担持体上に薄層を形成する工程を含む画像形成プロセス
において、凹凸度の大きなトナー粒子を用いると、薄層
形成時に付与される現像剤量規制体からの押圧力によっ
て当該トナー粒子が粉砕されて微細粒子を発生しやす
く、この微細粒子が、現像剤搬送担持体に対して強固に
付着して現像されにくくなる問題(選択現像)を生じ、
この選択現像によって、形成される画像の画像濃度が低
下してしまう。そして、トナー粒子の凹凸度を小さくす
ることはクリーニング性の向上を図る上で制限があり、
また、本発明者らが検討したところ、凹凸係数の大きい
トナー粒子が一定の割合で存在している場合には、トナ
ー粒子の凹凸係数や歪係数の平均値がある程度小さくて
も、選択現像による画像濃度の低下を十分に防止するこ
とができないことが確認された。(2) Selection Phenomenon As described above, it is preferable to use a toner having a large unevenness from the viewpoint of improving the cleaning property. However, in the image forming process including the step of forming a thin layer on the developer transport carrier by using the pressing force of the developer amount regulating member, if toner particles having a large unevenness are used, the toner particles are provided at the time of forming the thin layer. Due to the pressing force from the developer amount regulating body, the toner particles are easily crushed to generate fine particles, and the fine particles adhere firmly to the developer carrying carrier and are difficult to develop (selection). Development)
By this selective development, the image density of the formed image is reduced. Further, there is a limit to reducing the unevenness of the toner particles in order to improve the cleaning property,
In addition, as a result of examination by the present inventors, when toner particles having a large unevenness coefficient are present at a constant ratio, even if the average value of the unevenness coefficient and the distortion coefficient of the toner particles is small to some extent, the selective development It was confirmed that the reduction of the image density cannot be sufficiently prevented.
【0005】(3)画像不良 特開昭61−279864号公報に記載されている技
術、すなわち、使用するトナー粒子の歪係数および凹凸
係数について、各々の平均値を考慮する技術において、
これらの係数が過大である粒子または過小である粒子が
含有されている場合には、上記クリーニング不良の問題
および選択現像の問題を解決できないばかりか、トナー
粒子の帯電分布が広くなり過ぎて、形成される画像にカ
ブリ等の画像不良を発生させる。(3) Image Defect In the technique described in Japanese Patent Laid-Open No. 61-279864, that is, the technique in which the respective average values of the distortion coefficient and unevenness coefficient of the toner particles used are considered,
If the particles containing these coefficients are too large or too small, not only the above problems of cleaning failure and the problems of selective development cannot be solved but also the charge distribution of the toner particles becomes too wide, resulting in formation. An image defect such as a fog is generated in the formed image.
【0006】一方、流動性や帯電特性の向上等を図るべ
く、トナーおよびキャリアの凹凸係数やトナーの歪係数
等について規定した技術が紹介されている(特開平1−
185654号公報参照)。しかしながら、この技術に
おいても、凹凸係数や歪係数を算出するための最大長、
周長および面積は、それぞれ平均値として求められたも
のであって、上記の問題を解決する手段として十分な技
術であるといえない。On the other hand, in order to improve the fluidity and the charging property, a technique has been introduced which defines the unevenness coefficient of the toner and carrier, the distortion coefficient of the toner, etc.
185654). However, even in this technique, the maximum length for calculating the unevenness coefficient and the distortion coefficient,
The perimeter and the area are each obtained as an average value, and cannot be said to be a sufficient technique as a means for solving the above problems.
【0007】本発明は、以上のような事情に基いてなさ
れたものであって、本発明の第1の目的は、ブレードを
備えた装置によるクリーニング工程を含む画像形成方法
であって、クリーニング不良を発生させない画像形成方
法を提供することにある。本発明の第2の目的は、上記
のクリーニング工程および非接触現像工程を含む画像形
成方法であって、選択現像に起因する画像濃度の低下を
発生させない画像形成方法を提供することにある。本発
明の第3の目的は、カブリ等の画像不良を発生させない
画像形成方法を提供することにある。The present invention has been made under the above circumstances, and a first object of the present invention is an image forming method including a cleaning step by an apparatus equipped with a blade, which is defective in cleaning. An object of the present invention is to provide an image forming method which does not generate A second object of the present invention is to provide an image forming method including the above cleaning step and non-contact developing step, which does not cause a decrease in image density due to selective development. A third object of the present invention is to provide an image forming method that does not cause image defects such as fog.
【0008】[0008]
【課題を解決するための手段】本発明者らは、クリーニ
ング不良を招きやすい粒子形状および選択現像を招きや
すい粒子形状について、それぞれ個別に検討し、かつ、
トナー粒子全体の平均的な形状ではなくて粒子形状の分
布状態に着目した結果、特定の形状係数(凹凸係数)を
有する粒子のトナー粒子全体に対する個数比率を制御す
ることにより、クリーニング不良、選択現像を発生させ
ず、カブリ等の画像不良のない高画質の画像が得られる
ことを見出し、斯かる検知に基いて本発明を完成するに
至った。DISCLOSURE OF THE INVENTION The inventors of the present invention have individually examined the particle shape that tends to cause poor cleaning and the particle shape that tend to cause selective development, and
As a result of focusing on the distribution state of the particle shape rather than the average shape of the entire toner particle, cleaning failure and selective development can be performed by controlling the number ratio of particles having a specific shape coefficient (concave factor) to the entire toner particle. It was found that a high-quality image free of image defects such as fogging can be obtained without causing the above-mentioned problems, and the present invention has been completed based on such detection.
【0009】すなわち、本発明の画像形成方法は、ブレ
ードを備えたクリーニング装置によって像形成体上の転
写残留トナーを除去する工程を含む画像形成方法におい
て、この画像形成方法に用いる現像剤を構成するトナー
が下記の条件を満たすことを特徴とする。 <条件>形状係数Sを、S=(周長)2 /(面積×4
π)×100と定義するときに、 S<116となるトナー粒子のトナー粒子全体に対
する個数比率Aが30%以下であること。 S>145となるトナー粒子のトナー粒子全体に対
する個数比率Bが30%以下であること。 個数比率Aと個数比率Bとの合計が40%以下であ
ること。That is, the image forming method of the present invention constitutes a developer used in the image forming method in the image forming method including a step of removing the transfer residual toner on the image forming body by a cleaning device equipped with a blade. The toner is characterized by satisfying the following conditions. <Condition> The shape factor S is S = (perimeter) 2 / (area × 4)
When defined as π) × 100, the number ratio A of the toner particles with S <116 to the entire toner particles is 30% or less. The number ratio B of the toner particles with S> 145 to the entire toner particles is 30% or less. The total of the number ratio A and the number ratio B is 40% or less.
【0010】また、本発明の画像形成方法は、現像剤量
規制体の押圧力を利用することによって現像剤搬送担持
体上に付着した現像剤を薄層化し、この現像剤の薄層
を、像形成体に対して非接触となる状態で現像領域に搬
送し、前記現像剤搬送担持体に交流バイアス電圧を印加
して得られる振動電界下で像形成体上の静電潜像を現像
する工程と、ブレードを備えたクリーニング装置によっ
て像形成体上の転写残留トナーを除去する工程とを含む
画像形成方法において、この画像形成方法に用いる現像
剤を構成するトナーが上記の条件を満たすトナーである
ことを特徴とする。Further, in the image forming method of the present invention, by utilizing the pressing force of the developer amount regulating member, the developer adhering to the developer carrying carrier is thinned and the thin layer of the developer is The electrostatic latent image on the image forming body is developed under the oscillating electric field obtained by conveying the developing medium in a non-contact state to the image forming body and applying an AC bias voltage to the developer conveying carrier. In the image forming method including a step and a step of removing the transfer residual toner on the image forming body by a cleaning device equipped with a blade, the toner constituting the developer used in the image forming method is a toner satisfying the above conditions. It is characterized by being.
【0011】また、本発明の画像形成方法は、重合性単
量体を含む重合性組成物を水性媒体中で重合反応させて
得られる平均粒径0.1〜3μmの1次粒子が相互に会
合してなる平均粒径2〜6μmの2次粒子からなるトナ
ーと、樹脂被覆キャリアとを混合することにより製造さ
れる現像剤を用いることを特徴とする。In the image forming method of the present invention, primary particles having an average particle size of 0.1 to 3 μm, which are obtained by subjecting a polymerizable composition containing a polymerizable monomer to a polymerization reaction in an aqueous medium, are mutually separated. A developer produced by mixing a toner composed of secondary particles having an average particle diameter of 2 to 6 μm which are associated with each other and a resin-coated carrier is used.
【0012】[0012]
【作用】(1)凹凸係数の小さなトナー粒子が一定の割
合で存在している場合には、トナー粒子の凹凸係数の平
均値がある程度大きくてもクリーニング不良の発生を十
分に防止することはできない。本発明者らは、転写工程
の終了後に像形成体上に付着残留しているトナー粒子に
ついて、その粒子形状を観察したところ、特定形状のト
ナー粒子のみが残留していることを発見した。このこと
は、画像形成に用いたトナー粒子全体の平均的な形状に
関わらず、特定形状のトナー粒子のみがクリーニング不
良の発生に関与していることを意味する。そこで、本発
明者らは、当該特定形状のトナー粒子について着目すれ
ば、クリーニング不良の発生を抑制できるものと考え、
像形成体上に付着残留している特定形状のトナー粒子に
ついて、その形状係数S〔S=(周長)2 /(面積×4
π)×100〕を測定した。その結果、像形成体上に付
着残留しているトナー粒子の大部分は、形状係数Sが1
16未満の粒子であった。更に、トナー粒子全体に対す
る特定形状のトナー粒子の含有割合(個数比率)とクリ
ーニング性との関係について検討した結果、形状係数S
が116未満のトナー粒子の個数比率Aを30個数%以
下に制御することにより、良好なクリーニング性が発揮
されることを見出した。(1) When toner particles having a small unevenness coefficient are present at a constant ratio, it is not possible to sufficiently prevent defective cleaning even if the average value of the unevenness coefficient of the toner particles is large to some extent. . The present inventors have found that the toner particles adhering and remaining on the image forming body after the completion of the transfer step are observed for the particle shape, and that only the toner particles having a specific shape remain. This means that regardless of the average shape of the entire toner particles used for image formation, only the toner particles of a specific shape are involved in the occurrence of cleaning failure. Therefore, the inventors of the present invention think that the occurrence of cleaning failure can be suppressed by paying attention to the toner particles having the specific shape.
The shape factor S [S = (perimeter) 2 / (area × 4)
π) × 100] was measured. As a result, most of the toner particles remaining on the image forming body have a shape factor S of 1.
The particles were less than 16. Further, as a result of examining the relationship between the content ratio (number ratio) of the toner particles of a specific shape to the entire toner particles and the cleaning property, the shape factor S
It has been found that by controlling the number ratio A of the toner particles having a ratio of less than 116 to 30 number% or less, good cleaning properties are exhibited.
【0013】(2)凹凸係数の大きなトナー粒子が一定
の割合で存在している場合には、トナー粒子の凹凸係数
の平均値がある程度小さくても、選択現像による画像濃
度の低下を十分に防止することができない。そこで、本
発明者らが、用いるトナー粒子の形状係数Sと、現像剤
量規制体の押圧力による粉砕容易性との関係を検討した
ところ、形状係数Sが145を超える粒子を含有する場
合にトナー粒子の粉砕による微細粒子が発生しやすく、
形状係数Sが145を超えるトナー粒子の個数比率Bを
30個数%以下に制御することにより、選択現像等の発
生が防止されて適正な画像濃度を有する画像が形成され
ることを見出した。(2) In the case where toner particles having a large unevenness coefficient are present at a constant ratio, even if the average value of the unevenness coefficient of the toner particles is small to some extent, the decrease in image density due to selective development is sufficiently prevented. Can not do it. Therefore, the present inventors have examined the relationship between the shape factor S of the toner particles to be used and the easiness of crushing due to the pressing force of the developer amount regulating member. As a result, when the shape factor S contains particles exceeding 145, Fine particles are likely to be generated by crushing toner particles,
It has been found that by controlling the number ratio B of toner particles having a shape factor S exceeding 145 to 30% or less, the occurrence of selective development and the like is prevented and an image having an appropriate image density is formed.
【0014】(3)本発明においては、S<116とな
る粒子の個数比率Aと、S>145となる粒子の個数比
率Bとの合計(A+B)が40個数%以下であるので、
クリーニング不良の発生防止および選択現像の防止とい
う両目的をバランスよく満足するとともに、トナー粒子
の帯電分布がシャープとなり、形成される画像にカブリ
等の画像不良を発生させない。(3) In the present invention, the total (A + B) of the number ratio A of particles satisfying S <116 and the number ratio B of particles satisfying S> 145 is 40 number% or less.
Both the objectives of preventing the occurrence of defective cleaning and the prevention of selective development are satisfied in a well-balanced manner, and the charge distribution of toner particles becomes sharp, so that image defects such as fog do not occur in the formed image.
【0015】以下、本発明を具体的に説明する。 〔トナーの説明〕本発明においては、現像剤を構成する
トナー粒子の形状(凹凸度)分布が特定の範囲に規定さ
れている点に特徴を有するものである。具体的には、形
状係数Sを、「S=(周長)2 /(面積×4π)×10
0」と定義するときに、 S<116となるトナー粒
子の個数比率Aが30%以下、 S>145となるト
ナー粒子個数比率Bが30%以下、 個数比率(A+
B)が40%以下であることが条件とされる。The present invention will be specifically described below. [Description of Toner] The present invention is characterized in that the shape (irregularity) distribution of the toner particles constituting the developer is defined in a specific range. Specifically, the shape factor S is calculated as “S = (perimeter) 2 / (area × 4π) × 10
0 ", the toner particle number ratio A with S <116 is 30% or less, the toner particle number ratio B with S> 145 is 30% or less, and the number ratio (A +
The condition is that B) is 40% or less.
【0016】S<116となるトナー粒子の個数比率A
が30%以下であれば、他のクリーニング性が良好なト
ナー粒子(S≧116)が、研磨剤のように作用する結
果、ブレードによる良好なクリーニング性が発現され
る。しかし、個数比率Aが30%を超えると、このクリ
ーニング性が減殺されクリーニング不良が発生する。ま
た、S>145となるトナー粒子個数比率Bが30%以
下であれば現像性への影響も少ないが、この個数比率B
が30%を超えると、トナー粒子の粉砕による選択現像
が発生しやすくなり、形成される画像の画像濃度低下を
招くようになる。更に、個数比率(A+B)が40%を
超える場合には、摩擦帯電面積がトナー粒子間で極端に
異なるものとなって帯電分布がブロードとなる結果、カ
ブリ、トナー飛散等が発生しやすくなる。Number ratio A of toner particles with S <116
Is 30% or less, other toner particles having good cleaning properties (S ≧ 116) act like an abrasive, and as a result, good cleaning properties with a blade are exhibited. However, when the number ratio A exceeds 30%, this cleaning property is diminished and cleaning failure occurs. Further, if the toner particle number ratio B with S> 145 is 30% or less, the influence on the developing property is small, but this number ratio B
When it exceeds 30%, selective development due to pulverization of toner particles is likely to occur, resulting in a decrease in image density of an image formed. Further, when the number ratio (A + B) exceeds 40%, the triboelectrification areas become extremely different among the toner particles and the charge distribution becomes broad, so that fogging, toner scattering, etc. are likely to occur.
【0017】ここで形状係数Sは、トナー粒子の凹凸度
を表現するものであり、凹凸のない完全球形のトナー粒
子にあってはS=100となる。形状係数Sの測定は、
先ず、走査型電子顕微鏡を用いてトナー粒子の電子顕微
鏡写真を撮影し、次いで、ビデオカメラを用いて当該電
子顕微鏡写真を画像解析装置「SPICCA」(日本ア
ビオニクス(株)製)に入力し、例えば500個のトナ
ー粒子について、周長、面積を測定することにより行
う。なお、本発明においては、各トナー粒子ごとに周長
および面積を測定して個々の粒子について形状係数Sを
求める。Here, the shape factor S represents the degree of unevenness of the toner particles, and S = 100 for a perfectly spherical toner particle having no unevenness. The shape factor S is measured by
First, an electron micrograph of toner particles is taken using a scanning electron microscope, and then the electron micrograph is input to an image analyzer "SPICCA" (manufactured by Nippon Avionics Co., Ltd.) using a video camera. The measurement is performed by measuring the perimeter and area of 500 toner particles. In the present invention, the peripheral length and area of each toner particle are measured to obtain the shape factor S of each particle.
【0018】斯かるトナーを製造する方法としては、上
記の形状分布を満足するものが得られるのであれば特に
限定されるものではないが、目的とする形状や粒径を有
するトナー粒子を効率的に得られるという観点から、会
合型重合によって製造することが好ましい。具体的に
は、重合性単量体を含む重合性組成物を水性媒体中で重
合反応させて平均粒径0.1〜3μmの1次粒子を得、
次いで、この1次粒子を相互に会合させることにより、
平均粒径2〜6μmの2次粒子よりなるトナーを製造す
る方法を挙げることができる。この会合型重合によって
トナーを製造する場合においては、会合条件(時間)等
を調整することにより、得られるトナー粒子の形状係数
Sを上記の好適な範囲に制御することができる。The method for producing such a toner is not particularly limited as long as a toner satisfying the above-mentioned shape distribution can be obtained, but toner particles having a desired shape and particle diameter are efficiently used. From the viewpoint that it can be obtained, it is preferable to manufacture by associative polymerization. Specifically, a polymerizable composition containing a polymerizable monomer is subjected to a polymerization reaction in an aqueous medium to obtain primary particles having an average particle size of 0.1 to 3 μm,
Then, by associating these primary particles with each other,
A method of producing a toner composed of secondary particles having an average particle diameter of 2 to 6 μm can be mentioned. In the case of producing a toner by this associative polymerization, the shape factor S of the obtained toner particles can be controlled within the above-mentioned preferable range by adjusting the associating conditions (time) and the like.
【0019】前記1次粒子は、例えば乳化重合法によっ
て得られる。また、前記2次粒子は1次粒子同士がイオ
ン性結合、水素結合、金属配位結合、弱酸−弱塩基結
合、ファンデルワールス力による結合等によって接合し
ている粒子である。1次粒子を得るための単量体として
は、スチレン系単量体、アクリル系単量体、極性基を有
するその他の単量体等が挙げられる。The primary particles are obtained, for example, by an emulsion polymerization method. The secondary particles are particles in which the primary particles are bonded to each other by an ionic bond, a hydrogen bond, a metal coordination bond, a weak acid-weak base bond, a bond by Van der Waals force, or the like. Examples of the monomer for obtaining the primary particles include styrene-based monomers, acrylic-based monomers, and other polar group-containing monomers.
【0020】スチレン系単量体としては、スチレン、o
−メチルスチレン、m−メチルスチレン、p−メチルス
チレン、α−メチルスチレン、p−エチルスチレン、
2,4−ジメチルスチレン、p−n−ブチルスチレン、
p−tert−ブチルスチレン、p−n−ヘキシルスチ
レン、p−n−オクチルスチレン、p−n−ノニルスチ
レン、p−n−デシルスチレン、p−n−ドデシルスチ
レン、p−メトキシスチレン、p−フェニルスチレン、
p−クロルスチレン、3,4−ジクロルスチレン等が挙
げられる。アクリル系単量体としては、アクリル酸メチ
ル、アクリル酸エチル、アクリル酸n−ブチル、アクリ
ル酸イソブチル、アクリル酸プロピル、アクリル酸n−
オクチル、アクリル酸ドデシル、アクリル酸ラウリル、
アクリル酸−2−エチルヘキシル、アクリル酸ステアリ
ル、アクリル酸−2−クロルエチル、アクリル酸フェニ
ル、α−クロルアクリル酸メチル、メタクリル酸メチ
ル、メタクリル酸エチル、メタクリル酸プロピル、メタ
クリル酸n−ブチル、メタクリル酸イソブチル、メタク
リル酸n−オクチル、メタクリル酸ドデシル、メタクリ
ル酸ラウリル、メタクリル酸−2−エチルヘキシル、メ
タクリル酸ステアリル、メタクリル酸フェニル、メタク
リル酸ジメチルアミノエチル、メタクリル酸ジエチルア
ミノエチル等が挙げられる。The styrene-based monomer is styrene, o
-Methyl styrene, m-methyl styrene, p-methyl styrene, α-methyl styrene, p-ethyl styrene,
2,4-dimethylstyrene, pn-butylstyrene,
p-tert-butylstyrene, pn-hexylstyrene, pn-octylstyrene, pn-nonylstyrene, pn-decylstyrene, pn-dodecylstyrene, p-methoxystyrene, p-phenyl styrene,
Examples thereof include p-chlorostyrene and 3,4-dichlorostyrene. Acrylic monomers include methyl acrylate, ethyl acrylate, n-butyl acrylate, isobutyl acrylate, propyl acrylate, n-acrylate.
Octyl, dodecyl acrylate, lauryl acrylate,
2-ethylhexyl acrylate, stearyl acrylate, 2-chloroethyl acrylate, phenyl acrylate, α-chloromethyl acrylate, methyl methacrylate, ethyl methacrylate, propyl methacrylate, n-butyl methacrylate, isobutyl methacrylate , N-octyl methacrylate, dodecyl methacrylate, lauryl methacrylate, 2-ethylhexyl methacrylate, stearyl methacrylate, phenyl methacrylate, dimethylaminoethyl methacrylate, diethylaminoethyl methacrylate and the like.
【0021】極性基を有するその他の単量体としては、
下記のものが挙げられる。 (1)酸性極性基を有するもの アクリル酸、メタクリル酸、フマール酸、マレイン
酸、イタコン酸、ケイ皮酸、マレイン酸モノブチルエス
テル、マレイン酸モノオクチルエステル、またはこれら
の金属(Na,Zn等)塩類等のカルボキシル基(−C
OOH)を有するα,β−エチレン不飽和化合物。 スルホン化スチレンまたはそのNa塩、アリルスル
ホコハク酸、アリルスルホコハク酸オクチルまたはその
Na塩等のスルホン基(−SO3 H)を有するα,β−
エチレン性不飽和化合物。Other monomers having a polar group include
The following are listed. (1) Having acidic polar group Acrylic acid, methacrylic acid, fumaric acid, maleic acid, itaconic acid, cinnamic acid, maleic acid monobutyl ester, maleic acid monooctyl ester, or metal thereof (Na, Zn, etc.) Carboxyl group (-C
Α, β-ethylenically unsaturated compound having OOH). Α, β- having a sulfo group (-SO 3 H) such as sulfonated styrene or its Na salt, allylsulfosuccinic acid, octyl allylsulfosuccinate or its Na salt
Ethylenically unsaturated compounds.
【0022】(2)塩基性極性基を有するもの ジメチルアミノエチルアクリレート、ジメチルアミ
ノエチルメタクリレート、ジエチルアミノエチルアクリ
レート、ジエチルアミノエチルメタクリレート、これら
の化合物の四級アンモニウム塩、3−ジメチルアミノフ
ェニルアクリレート、2−ヒドロキシ−3−メタクリル
オキシプロピルトリメチルアンモニウム塩等のアミン基
または四級アンモニウム塩基を有する炭素原子数1〜1
2の脂肪族アルコールの(メタ)アクリル酸エステル。 アクリルアミド、N−ブチルアクリルアミド、N,
N−ジブチルアクリルアミド、ピペリジルアクリルアミ
ド、メタクリルアミド、N−ブチルメタクリルアミド、
N,N−ジメチルアクリルアミド、N−オクタデシルア
クリルアミド等の(メタ)アクリル酸アミドまたはN上
で随意モノマーもしくはジ−アルキル置換された(メ
タ)アクリル酸アミド。 ビニールピリジン、ビニールピロリドン、ビニール
N−メチルピリジニウムクロリド、ビニールN−エチル
ピリジニウムクロリド等のNを環員として有する複素環
基で置換されたビニール化合物。 N,N−ジアリルメチルアンモニウムクロリド、
N,N−ジアリルエチルアンモニウムクロリド等のN,
N−ジアリルアルキルアミン。(2) Having a basic polar group: dimethylaminoethyl acrylate, dimethylaminoethyl methacrylate, diethylaminoethyl acrylate, diethylaminoethyl methacrylate, quaternary ammonium salts of these compounds, 3-dimethylaminophenyl acrylate, 2-hydroxy. -3-Methacryloxypropyltrimethylammonium salt or other amine group or quaternary ammonium salt group having 1 to 1 carbon atoms
(Meth) acrylic acid ester of aliphatic alcohol of 2. Acrylamide, N-butyl acrylamide, N,
N-dibutyl acrylamide, piperidyl acrylamide, methacrylamide, N-butyl methacrylamide,
(Meth) acrylic acid amides such as N, N-dimethylacrylamide, N-octadecylacrylamide or (meth) acrylic acid amides optionally substituted on N or di-alkyl. A vinyl compound substituted with a heterocyclic group having N as a ring member such as vinyl pyridine, vinyl pyrrolidone, vinyl N-methylpyridinium chloride and vinyl N-ethylpyridinium chloride. N, N-diallylmethylammonium chloride,
N, such as N, N-diallylethylammonium chloride,
N-diallylalkylamine.
【0023】1次粒子を得るための単量体において、ス
チレン系単量体とアクリル系単量体の配合割合 (重量
比) は、90〜20:10〜80が好ましく、特に70
〜30:30〜70が好ましい。極性基を有するその他
の単量体の配合割合は、スチレン系単量体とアクリル系
単量体の合計100重量部に対して、0.05〜30重
量部が好ましく、特に1〜20重量部が好ましい。In the monomer for obtaining the primary particles, the mixing ratio (weight ratio) of the styrene monomer and the acrylic monomer is preferably 90 to 20:10 to 80, and particularly 70
-30: 30-70 is preferable. The mixing ratio of the other monomer having a polar group is preferably 0.05 to 30 parts by weight, particularly 1 to 20 parts by weight, based on 100 parts by weight of the total of the styrene-based monomer and the acrylic-based monomer. Is preferred.
【0024】1次粒子を得るための重合用組成物中に
は、必要に応じて種々の添加剤が含有されていてもよ
い。かかる添加剤としては、着色剤、離型剤、荷電制御
剤等を挙げることができる。着色剤としては、カーボン
ブラック、ニグロシン染料、アニリンブルー、カルコオ
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、ランプブラック、ローズベンガ
ル、これらの混合物、その他が挙げられる。離型剤とし
ては、低軟化点のポリオレフィン、高融点パラフィンワ
ックス、シリコーンワニス、脂肪族エステル類またはそ
の部分ケン化物類、脂肪族アミド系化合物、高級アルコ
ール等が挙げられる。荷電制御剤としては、金属錯体系
染料、ニグロシン系染料、アンモニウム塩系化合物等が
挙げられる。If desired, various additives may be contained in the composition for polymerization for obtaining the primary particles. Examples of such additives include colorants, release agents, charge control agents, and the like. As the colorant, carbon black, nigrosine dye, aniline blue, chalco oil blue, chrome yellow, ultramarine blue,
DuPont Oil Red, Quinoline Yellow, Methylene Blue Chloride, Phthalocyanine Blue, Malachite Green Oxalate, Lamp Black, Rose Bengal, mixtures thereof and the like. Examples of the releasing agent include low softening point polyolefin, high melting point paraffin wax, silicone varnish, aliphatic ester or partially saponified product thereof, aliphatic amide compound, and higher alcohol. Examples of the charge control agent include metal complex dyes, nigrosine dyes, ammonium salt compounds, and the like.
【0025】また、以上のようにして得られたトナーに
無機微粒子等の外部添加剤を添加してもよい。無機微粒
子としては、例えばシリカ、アルミナ、酸化チタン、チ
タン酸バリウム、チタン酸マグネシウム、チタン酸カル
シウム、チタン酸ストロンチウム、酸化亜鉛、酸化クロ
ム、酸化セリウム、三酸化アンチモン、酸化ジルコニウ
ム、炭化ケイ素等の微粒子が挙げられる。中でも、シリ
カが好ましい。また、耐久性の観点からは、表面が疎水
化処理された無機微粒子が好ましい。Further, external additives such as inorganic fine particles may be added to the toner obtained as described above. Examples of the inorganic fine particles include fine particles of silica, alumina, titanium oxide, barium titanate, magnesium titanate, calcium titanate, strontium titanate, zinc oxide, chromium oxide, cerium oxide, antimony trioxide, zirconium oxide, silicon carbide and the like. Is mentioned. Of these, silica is preferable. Further, from the viewpoint of durability, inorganic fine particles whose surface is subjected to a hydrophobic treatment are preferable.
【0026】〔キャリアの説明〕本発明に用いるキャリ
アとしては特に限定されるものではないが、芯材粒子の
表面が樹脂により被覆されてなる樹脂被覆キャリアであ
ることが好ましい。キャリアの被覆用樹脂としては、特
に限定されず、例えばシリコーン系樹脂、フッ素系樹
脂、スチレン−アクリル系樹脂等が代表的なものとして
挙げられる。[Explanation of Carrier] The carrier used in the present invention is not particularly limited, but a resin-coated carrier in which the surface of core material particles is coated with a resin is preferable. The resin for coating the carrier is not particularly limited, and typical examples thereof include silicone resins, fluorine resins, styrene-acrylic resins and the like.
【0027】シリコーン系樹脂としては、シリコーンワ
ニス、シリコーンゴム、シリコーン樹脂等が挙げられる
が、構成単位としてアルキル基、芳香族基等の有機基を
有するものが好ましく、特にメチル基、フェニル基等の
有機基を有するものが好ましい。かかる有機基を有する
シリコーン系樹脂を得るための化合物としては、ジメチ
ルポリシロキサン、メチルフェニルポリシロキサン、ジ
フェニルポリシロキサン、これらの変性体等が挙げられ
る。特に、メチル基またはフェニル基を有するポリシロ
キサンは、優れた負帯電性を有する。また、上記有機基
において、メチル基、フェニル基の含有割合を適宜選択
することにより、キャリアの被覆層の硬度、強靱性、摩
擦帯電性等の特性を調整することができ、従って、樹脂
被覆キャリアと組み合わせて用いるトナーに必要とされ
る条件が相当に緩和され、トナーの選択範囲が広範とな
る。Examples of the silicone-based resin include silicone varnish, silicone rubber, silicone resin and the like, but those having an organic group such as an alkyl group or an aromatic group as a constitutional unit are preferable, and a methyl group or a phenyl group is particularly preferable. Those having an organic group are preferable. Examples of the compound for obtaining the silicone-based resin having such an organic group include dimethylpolysiloxane, methylphenylpolysiloxane, diphenylpolysiloxane, and modified products thereof. In particular, polysiloxane having a methyl group or a phenyl group has an excellent negative charging property. Further, in the above organic group, by appropriately selecting the content ratios of the methyl group and the phenyl group, it is possible to adjust the characteristics such as hardness, toughness, and triboelectricity of the coating layer of the carrier. The conditions required for the toner used in combination with are considerably relaxed, and the selection range of the toner becomes wide.
【0028】シリコーンワニスの市販品としては、SR
2101、SH997、SH994、SR2202、S
E9140、SH643、SH2047、JCR610
0、JCR6101(以上、トーレ・シリコーン社
製)、KR271、KR272、KR274、KR21
6、KR280、KR282、KR261、KR26
0、KR255、KR266、KR251、KR15
5、KR152、KR214、KR220、X−4040
−171、KR201、SA−4、KR5202、KR
3093、EC1001 (以上、信越化学工業社製) 等
が挙げられる。シリコーンゴムの市販品としては、SH
410、SH432、SH433、SH740、SH3
5U、SH75U、SH841U、SH1125U、S
H1603U、SH665U、SE955U、SH50
2U、SRX−440U(以上、トーレ・シリコーン社
製)等が挙げられる。Commercially available products of silicone varnish are SR
2101, SH997, SH994, SR2202, S
E9140, SH643, SH2047, JCR610
0, JCR6101 (above, manufactured by Toray Silicone Co., Ltd.), KR271, KR272, KR274, KR21
6, KR280, KR282, KR261, KR26
0, KR255, KR266, KR251, KR15
5, KR152, KR214, KR220, X-4040
-171, KR201, SA-4, KR5202, KR
3093, EC1001 (above, manufactured by Shin-Etsu Chemical Co., Ltd.) and the like. Commercially available silicone rubber is SH
410, SH432, SH433, SH740, SH3
5U, SH75U, SH841U, SH1125U, S
H1603U, SH665U, SE955U, SH50
2U, SRX-440U (above, made by Toray Silicone Co., Ltd.), etc. are mentioned.
【0029】フッ素系樹脂としては、フッ素原子が含ま
れている樹脂であれば特に限定されず、例えば下記化1
の一般式(1)または(2)で表される単量体を重合し
てなる重合体、フッ化ビニリデン−四フッ化エチレン共
重合体等が挙げられる。The fluorine-based resin is not particularly limited as long as it is a resin containing a fluorine atom, and for example, the following chemical formula 1
And a polymer obtained by polymerizing the monomer represented by the general formula (1) or (2), a vinylidene fluoride-tetrafluoroethylene copolymer, and the like.
【0030】[0030]
【化1】 [Chemical 1]
【0031】(式中、R1 ,R2 はそれぞれ水素原子ま
たはメチル基を表し、n,pはそれぞれ1〜8の整数を
表し、m,qはそれぞれ1〜19の整数を表す。)上記
一般式(1)または(2)で示される単量体のうち、特
に摩擦帯電性の点において下記化2の一般式(3)また
は(4)で表される単量体が好ましい。(In the formula, R 1 and R 2 each represent a hydrogen atom or a methyl group, n and p each represent an integer of 1 to 8, and m and q each represent an integer of 1 to 19). Among the monomers represented by the general formula (1) or (2), the monomer represented by the general formula (3) or (4) of the following chemical formula 2 is preferable in terms of triboelectric charging property.
【0032】[0032]
【化2】 [Chemical 2]
【0033】(式中、R3 ,R4 はそれぞれ水素原子ま
たはメチル基を表し、rは1〜2の整数を表し、sは2
〜4の整数を表す。)また、前記一般式(1)または
(2)で示される単量体のうち、特に、メタクリル酸−
1,1−ジヒドロパーフルオロエチル、メタクリル酸−
1,1,3−トリヒドロパーフルオロ−n−プロピル等
が好ましい。また、フッ化ビニリデン−四フッ化エチレ
ン共重合体を用いる場合においては、これらの共重合モ
ル比は75:25〜95:5の範囲が好ましく、特に7
5:25〜87.5:12.5の範囲が好ましい。この
ような範囲にあれば、被覆層の形成に用いられる被覆液
の調製が容易となり、また得られる被覆層の機械的強度
が大きくて耐久性の優れた樹脂被覆キャリアが得られ
る。フッ素系樹脂の具体例としては下記化3および化4
に掲げるものが挙げられるが、これらに限定されるもの
ではない。なお、以下の具体例においてnは1以上の整
数を表す。(In the formula, R 3 and R 4 each represent a hydrogen atom or a methyl group, r represents an integer of 1 to 2, and s represents 2
Represents an integer of 4; In addition, among the monomers represented by the general formula (1) or (2), methacrylic acid-
1,1-dihydroperfluoroethyl, methacrylic acid-
1,1,3-trihydroperfluoro-n-propyl and the like are preferable. When a vinylidene fluoride-tetrafluoroethylene copolymer is used, the copolymerization molar ratio of these is preferably 75:25 to 95: 5, particularly 7
The range of 5:25 to 87.5: 12.5 is preferable. Within such a range, the coating solution used for forming the coating layer can be easily prepared, and a resin-coated carrier having a large mechanical strength and excellent durability can be obtained. Specific examples of the fluorine-based resin include the following chemical formulas 3 and 4
However, the present invention is not limited to these. In the following specific examples, n represents an integer of 1 or more.
【0034】[0034]
【化3】 [Chemical 3]
【0035】[0035]
【化4】 [Chemical 4]
【0036】スチレン−アクリル系樹脂は、スチレン系
単量体とアクリル系単量体から合成される。スチレン系
単量体およびアクリル系単量体としては、トナーにおけ
る1次粒子を得るための単量体として例示したスチレン
系単量体、アクリル系単量体と同様のものが用いられ
る。スチレン系単量体と、アクリル系単量体の組成比
は、重量比で9:1〜1:9であることが好ましい。ス
チレン成分は被覆層を硬くし、アクリル成分は被覆層を
強靱なものとする。また、これらの組成比を適宜変更す
ることにより、樹脂被覆キャリアとトナーとの摩擦帯電
におけるトナーの帯電量を相当程度制御することができ
る。また、スチレン−アクリル系樹脂の分子量は、被覆
層の固着強度を高めて耐久性の向上を図る観点から、重
量平均分子量Mwが30,000〜200,000であ
ることが好ましい。The styrene-acrylic resin is synthesized from a styrene monomer and an acrylic monomer. As the styrene-based monomer and the acrylic-based monomer, those similar to the styrene-based monomer and the acrylic-based monomer exemplified as the monomer for obtaining the primary particles in the toner are used. The weight ratio of the styrene-based monomer to the acrylic-based monomer is preferably 9: 1 to 1: 9. The styrene component makes the coating layer hard and the acrylic component makes the coating layer tough. Further, by appropriately changing the composition ratio of these, it is possible to considerably control the charge amount of the toner in the frictional charging between the resin-coated carrier and the toner. Further, the molecular weight of the styrene-acrylic resin is preferably a weight average molecular weight Mw of 30,000 to 200,000 from the viewpoint of enhancing the fixing strength of the coating layer and improving the durability.
【0037】樹脂被覆キャリアは、被覆用樹脂を有機溶
媒に溶解して被覆液を調製し、この被覆液を例えば浸漬
法、スプレードライ法、流動化ベッド法等の方法により
キャリアの芯材粒子の表面に塗布して被覆層を形成した
後、さらに加熱または放置等によって形成することがで
きる。また、特開昭63−235959号公報に示され
た乾式コーティング法によっても形成することができ
る。樹脂被覆キャリアの芯材粒子としては、従来公知の
材料が用いられ、例えばフェライト、マグネタイト、鉄
等の強磁性体材料が好ましく用いられる。樹脂被覆キャ
リアの重量平均粒径は、通常10〜300μmが好まし
く、特に20〜100μmが好ましい。The resin-coated carrier is prepared by dissolving a coating resin in an organic solvent to prepare a coating solution, and using this coating solution, for example, a dipping method, a spray drying method, a fluidized bed method, etc. The coating layer can be formed by applying it to the surface to form a coating layer, and then further heating or standing. It can also be formed by the dry coating method disclosed in JP-A-63-235959. As the core particles of the resin-coated carrier, conventionally known materials are used, and for example, ferromagnetic materials such as ferrite, magnetite and iron are preferably used. The weight average particle diameter of the resin-coated carrier is usually preferably 10 to 300 μm, and particularly preferably 20 to 100 μm.
【0038】〔画像形成プロセスの説明〕図1は、本発
明に使用することができる像形成装置の一例を示す概略
説明図である。この像形成装置においては、原稿台10
が移動することにより、照明光源11で照射された原稿
像がミラー12、レンズ13を介して像形成体14上に
照射され、これにより静電潜像が形成される。この静電
潜像は現像装置Hにより現像され、トナー像が形成され
る。次いで、このトナー像は、露光ランプ15により除
電されて転写されやすくされた後、転写極16により記
録紙Pに転写される。トナー像が転写された記録紙Pは
分離極17により像形成体14から分離され、定着器3
1で定着される。一方、像形成体14上の転写残トナー
は除電極32およびクリーニング装置33により除去さ
れる。このクリーニング装置33は、転写残トナーを掻
き取るブレード34と、掻き取られたトナーを捕集する
ローラ36とにより構成されている。[Description of Image Forming Process] FIG. 1 is a schematic explanatory view showing an example of an image forming apparatus that can be used in the present invention. In this image forming apparatus, the document table 10
Is moved, the original image emitted from the illumination light source 11 is emitted onto the image forming body 14 via the mirror 12 and the lens 13, thereby forming an electrostatic latent image. This electrostatic latent image is developed by the developing device H to form a toner image. Next, the toner image is discharged by the exposure lamp 15 to facilitate transfer, and then transferred to the recording paper P by the transfer pole 16. The recording paper P on which the toner image has been transferred is separated from the image forming body 14 by the separation pole 17, and the fixing device 3
It is fixed at 1. On the other hand, the transfer residual toner on the image forming body 14 is removed by the removing electrode 32 and the cleaning device 33. The cleaning device 33 includes a blade 34 for scraping off the transfer residual toner and a roller 36 for collecting the scraped toner.
【0039】図2は、上記の像形成装置に搭載される非
接触現像装置の構成を示す概略説明図である。同図にお
いて、20は現像剤搬送担持体であり、この現像剤搬送
担持体20は、矢印方向に回転するN,S交互の磁極8
極を有する磁石ロール21と、この磁石ロール21と反
対方向に回転して現像剤層を現像領域Kに搬送する現像
スリーブ22とにより構成されている。23は、現像ス
リーブ22を押圧して現像剤層の層厚を規制する弾性圧
接板からなる現像剤量規制体、24は、振動電界を形成
するための交流バイアス電源、25および26は、矢印
方向に回転する攪拌装置、27はトナー補給ローラ、2
8はトナーホッパ、Tは補給用トナーである。磁石ロー
ル21の現像領域における磁極の強さ(磁束密度)は5
00〜1500ガウスとされ、この磁石ロール21は、
現像スリーブ22と同方向に回転されてもよく、固定さ
れてもよい。また、磁極数は4〜20 極の範囲で適宜選
定されてよいが、現像剤をむらなく搬送する観点から6
極以上とすることが好ましい。現像スリーブ22は、
銅、アルミニウム、マグネシウム等の非磁石材料から構
成されるものであることが好ましく、必要により、サン
ドブラスト等により表面を粗面とし、また、表面を高抵
抗としてもよい。現像剤量規制体23の押圧力としては
0.1〜5g/cmとされ、2成分現像剤からなる現像
剤層の非接触現像を行う際に望まれる20〜500μm
の薄い現像剤層を形成する上で好適なものとされる。な
お、現像領域Kにおいて、矢印方向に回転する像形成体
14と現像スリーブ22との間隙は現像剤層厚より大き
く、通常100〜1000μmとされ、振動電界下での
非接触現像を可能にするように設定される。交流バイア
ス電源24により、通常100Hz〜10kHz、好ま
しくは1〜5kHzの周波数で、通常0.2〜3.0K
V(P−P)、好ましくは1.0〜2.0KV(P−
P)のバイアスが印加される。さらに、カブリの発生を
防止するため、正規現像の場合には、静電潜像と同極性
の直流バイアスが50〜500V重畳して印加され、反
転現像の場合には、静電潜像電位に近い直流バイアスが
印加される。攪拌装置25,26には、それぞれの回転
軸に傾斜した攪拌羽根が複数設けられ、かつ、それぞれ
の攪拌羽根は互いに衝突することなく同一領域を重複し
て回転するように設計されている。従って、現像剤は回
転軸方向およびその直角方向に移動攪拌され、現像剤の
摩擦帯電および均一な混合が十分に達成される。FIG. 2 is a schematic explanatory view showing the structure of a non-contact developing device mounted on the above image forming apparatus. In the figure, reference numeral 20 denotes a developer carrying carrier, and this developer carrying carrier 20 has N and S alternating magnetic poles 8 which rotate in the arrow direction.
It is composed of a magnet roll 21 having a pole and a developing sleeve 22 which rotates in the opposite direction to the magnet roll 21 and conveys the developer layer to the developing area K. Reference numeral 23 is a developer amount regulating body composed of an elastic pressure contact plate that presses the developing sleeve 22 to regulate the layer thickness of the developer layer, 24 is an AC bias power source for forming an oscillating electric field, and 25 and 26 are arrows. Agitating device that rotates in a direction, 27 is a toner replenishing roller, 2
Reference numeral 8 is a toner hopper, and T is a replenishment toner. The magnetic pole strength (magnetic flux density) in the developing area of the magnet roll 21 is 5
This magnet roll 21 is set to have a Gauss of from 0 to 1500 gauss.
It may be rotated in the same direction as the developing sleeve 22 or may be fixed. Further, the number of magnetic poles may be appropriately selected within the range of 4 to 20 poles, but it is 6 from the viewpoint of evenly conveying the developer.
It is preferable that the number is extremely high. The developing sleeve 22 is
It is preferably made of a non-magnetic material such as copper, aluminum or magnesium. If necessary, the surface may be roughened by sandblasting or the like, and the surface may have high resistance. The pressing force of the developer amount regulator 23 is set to 0.1 to 5 g / cm and is desired to be 20 to 500 μm when performing non-contact development of a developer layer composed of a two-component developer.
It is suitable for forming a thin developer layer. In the developing area K, the gap between the image forming body 14 rotating in the direction of the arrow and the developing sleeve 22 is larger than the developer layer thickness and is usually 100 to 1000 μm, which enables non-contact development under an oscillating electric field. Is set as follows. With an AC bias power supply 24, usually at a frequency of 100 Hz to 10 kHz, preferably 1 to 5 kHz, usually 0.2 to 3.0 K
V (PP), preferably 1.0 to 2.0 KV (PP-
The bias of P) is applied. Further, in order to prevent the occurrence of fog, in the case of regular development, a DC bias of the same polarity as that of the electrostatic latent image is applied by being superposed by 50 to 500 V, and in the case of reversal development, the electrostatic latent image potential is applied. A close DC bias is applied. The stirring devices 25 and 26 are provided with a plurality of stirring blades inclined to their respective rotation axes, and each stirring blade is designed so as to rotate in the same region in an overlapping manner without colliding with each other. Therefore, the developer is moved and agitated in the direction of the rotation axis and in the direction perpendicular thereto, and the triboelectrification and uniform mixing of the developer are sufficiently achieved.
【0040】[0040]
【実施例】以下、本発明の実施例について説明するが、
本発明はこれらの実施例に限定されるものではない。な
お、以下において「部」は重量部を表す。EXAMPLES Examples of the present invention will be described below.
The invention is not limited to these examples. In addition, "part" represents a weight part below.
【0041】〔トナーの製造〕 (1)トナー1 水100部と、ポリオキシエチレンアルキルエーテル1
部と、アルキルベンゼンスルホン酸ナトリウム1.5部
と、過硫酸カリウム0.5部との水溶液混合物に、スチ
レン60部と、アクリル酸ブチル40部と、アクリル酸
8部とからなるモノマー混合物(重合性組成物)を添加
し、撹拌下70℃で8時間重合させて固形分濃度50%
の1次粒子のエマルジョンを得た。前記1次粒子のエマ
ルジョン120部と、ニグロシン5部と、顔料(カーボ
ンブラック)4部と、水380部との混合物をスラッシ
ャーで分散撹拌しながら約30℃で2時間保持した。そ
の後、さらに撹拌しながら70℃に加温して3時間保持
した。この間顕微鏡で観察して、1次粒子が会合して2
次粒子が得られるのが確認された。その後、冷却して、
得られた液状分散物をブフナー濾過、水洗し、50℃で
10時間にわたり真空乾燥を行い、トナー1を得た。[Production of Toner] (1) Toner 1 100 parts of water and polyoxyethylene alkyl ether 1
Part, 1.5 parts of sodium alkylbenzene sulfonate, and 0.5 parts of potassium persulfate in an aqueous solution mixture, 60 parts of styrene, 40 parts of butyl acrylate, and 8 parts of acrylic acid as a monomer mixture (polymerizable). Composition) and polymerized at 70 ° C. for 8 hours with stirring to obtain a solid content of 50%.
An emulsion of primary particles was obtained. A mixture of 120 parts of the primary particle emulsion, 5 parts of nigrosine, 4 parts of pigment (carbon black), and 380 parts of water was held at about 30 ° C. for 2 hours while being dispersed and stirred with a slasher. Then, the temperature was raised to 70 ° C. with further stirring, and the temperature was maintained for 3 hours. During this time, when observed with a microscope, the primary particles associate
It was confirmed that secondary particles were obtained. Then cool down,
The obtained liquid dispersion was subjected to Buchner filtration, washed with water, and vacuum dried at 50 ° C. for 10 hours to obtain toner 1.
【0042】(2)比較トナー1 トナー1の製造において、70℃における保持時間を1
時間に変更したこと以外は同様にして、比較トナー1を
得た。 (3)比較トナー2 トナー1の製造において、70℃における保持時間を7
時間に変更したこと以外は同様にして、比較トナー2を
得た。 (4)比較トナー3 前記比較トナー1と比較トナー2とを適宜混合して、比
較トナー3を得た。(2) Comparative Toner 1 In the production of Toner 1, the holding time at 70 ° C. is 1
Comparative Toner 1 was obtained in the same manner except that the time was changed. (3) Comparative Toner 2 In the production of Toner 1, the holding time at 70 ° C. was set to 7
Comparative Toner 2 was obtained in the same manner except that the time was changed. (4) Comparative Toner 3 The comparative toner 1 and the comparative toner 2 were appropriately mixed to obtain a comparative toner 3.
【0043】〔形状係数Sの測定〕上記のようにして得
られたトナー1および比較トナー1〜3の各々につい
て、走査型電子顕微鏡を用いてトナー粒子の電子顕微鏡
写真(倍率3500倍)を撮影した。次いで、ビデオカ
メラ(倍率4.5倍)を用いて当該電子顕微鏡写真を画
像解析装置「SPICCA」(日本アビオニクス(株)
製)に入力し、500個のトナー粒子の各々について、
周長、面積を測定して形状係数Sを求めた。これらのト
ナーの平均粒径および形状係数Sの個数比率を表1に示
す。[Measurement of Shape Coefficient S] With respect to each of Toner 1 and Comparative Toners 1 to 3 obtained as described above, an electron microscope photograph (magnification 3500 times) of toner particles is taken by using a scanning electron microscope. did. Then, using a video camera (magnification: 4.5 times), the electron micrograph is taken and the image analysis device "SPICCA" (Japan Avionics Co., Ltd.)
Manufactured) and for each of the 500 toner particles,
The shape factor S was obtained by measuring the circumference and the area. Table 1 shows the average particle size and the number ratio of the shape factor S of these toners.
【0044】[0044]
【表1】 [Table 1]
【0045】〔キャリアの製造〕通常の混合攪拌装置を
用いて、Cu−Znフェライト粒子と、フッ化ビニリデ
ン−四フッ化エチレン共重合体「VT−100」(共重
合モル比:80:20,ダイキン工業社製)と、メタク
リル酸メチル共重合体「アクリペットMF」(三菱レイ
ヨン社製)とを混合攪拌し、次いで得られた混合物を通
常の衝撃式粉砕装置を改良した装置に仕込み、当該装置
を通常の粉砕を行うときの約1/10程度の回転数で駆
動して、当該混合物に衝撃力を15分間にわたり繰り返
して付与して樹脂被覆キャリアを得た。[Production of Carrier] Cu—Zn ferrite particles and a vinylidene fluoride-tetrafluoroethylene copolymer “VT-100” (copolymerization molar ratio: 80:20, using a conventional mixing and stirring device). (Manufactured by Daikin Industries, Ltd.) and a methyl methacrylate copolymer “Acrypet MF” (manufactured by Mitsubishi Rayon Co., Ltd.) were mixed and stirred, and then the obtained mixture was charged into an apparatus improved from an ordinary impact pulverization apparatus. The device was driven at a rotation speed of about 1/10 of that during normal crushing, and impact force was repeatedly applied to the mixture for 15 minutes to obtain a resin-coated carrier.
【0046】〔現像剤の調製〕 (1)現像剤1 トナー1の50部に、疎水性シリカ1.2部を加え、こ
れをヘンシェルミキサーにより混合することによりトナ
ー粒子の表面に無機微粒子を保持させた後、これに前記
樹脂被覆キャリア950部を添加混合して本発明用の現
像剤1を調製した。 (2)比較現像剤1〜3 トナー1に代えて比較トナー1〜3を用いたこと以外は
現像剤1の調製方法と同様にして比較現像剤1〜3を調
製した。[Preparation of Developer] (1) Developer 1 To 50 parts of Toner 1, 1.2 parts of hydrophobic silica is added and mixed with a Henschel mixer to retain inorganic fine particles on the surface of the toner particles. After that, 950 parts of the above resin-coated carrier was added and mixed to prepare a developer 1 for the present invention. (2) Comparative Developers 1 to 3 Comparative Developers 1 to 3 were prepared in the same manner as the developer 1 except that Comparative Toners 1 to 3 were used instead of Toner 1.
【0047】〔実施例1〕現像剤として前記現像剤1を
用い、非接触式反転現像型の画像形成装置「DC902
8」(コニカ(株)製)改造機により、像形成体上にブ
ラックのトナー像を形成し、このトナー像を転写紙に転
写し、次いで定着して定着画像を形成する実写テストを
2万回にわたって行い、画像濃度安定性、クリーニング
性、カブリの発生の有無について評価した。[Embodiment 1] A non-contact reversal development type image forming apparatus "DC902" using the developer 1 as a developer.
8 "(manufactured by Konica Corp.) modified machine to form a black toner image on the image forming body, transfer the toner image onto transfer paper, and then fix it to form a fixed image. The image density stability, the cleaning property, and the presence or absence of fog were evaluated.
【0048】〔比較例1〜3〕現像剤1に代えて比較現
像剤1〜3の各々を用いたこと以外は実施例1と同様に
して実写テストを行い、画像濃度安定性、クリーニング
性、カブリの発生の有無について評価した。なお、比較
例2については100回の画像形成で、比較例3につい
ては300回の画像形成で実写テストを中止した。[Comparative Examples 1 to 3] An actual copying test was conducted in the same manner as in Example 1 except that the comparative developers 1 to 3 were used instead of the developer 1, and the image density stability, cleaning property, and The presence or absence of fog was evaluated. The image-forming test was stopped after 100 times of image formation in Comparative Example 2 and 300 times of image formation in Comparative Example 3.
【0049】 画像濃度安定性 画像形成初期および2万回形成後における画像濃度を測
定することにより、画像濃度安定性を評価した。画像濃
度の測定としては、黒色ベタ画像を形成し、この画像の
任意の8点をマクベス濃度計「マクベスRD918」に
より測定して反射濃度を求めて、その平均値を画像濃度
とした。 クリーニング性 ブレードを備えた装置によりクリーニングされた直後の
像形成体の表面を目視により観察し、当該像形成体の表
面における付着物の有無を観察した。この観察は100
回の画像形成ごとに行い、多くの付着物が認められ、画
像乱れ等実用的に問題が発生した時点のコピー回数を測
定した。 カブリ マクベス濃度計「マクベスRD918」を用いて非画像
部分の濃度を100コピーごとに測定し、濃度が0.0
1以上になった時点をカブリの発生とし、その時点での
コピー回数を測定した。これらの評価結果を表2に示
す。Image Density Stability Image density stability was evaluated by measuring the image density at the initial stage of image formation and after 20,000 times formation. The image density was measured by forming a black solid image, measuring arbitrary 8 points of this image with a Macbeth densitometer "Macbeth RD918" to obtain the reflection density, and taking the average value as the image density. Cleanability The surface of the image forming body immediately after being cleaned by a device equipped with a blade was visually observed to observe the presence or absence of deposits on the surface of the image forming body. This observation is 100
The number of copies was measured at each time when image formation was repeated and many deposits were observed, and when practical problems such as image distortion occurred. The density of the non-image area was measured every 100 copies using the Kaburi Macbeth densitometer "Macbeth RD918".
Fog was defined as the time when the number became 1 or more, and the number of copies at that time was measured. The results of these evaluations are shown in Table 2.
【0050】[0050]
【表2】 [Table 2]
【0051】なお、比較例1において、2万回形成後に
おいて測定されたトナー粒子の平均粒径は3.0μmで
あり、トナー粒子の粉砕が確認された。また、その際に
発生した微粉によって1万回コピー以降ではカブリが発
生した。In Comparative Example 1, the average particle diameter of the toner particles measured after forming 20,000 times was 3.0 μm, and it was confirmed that the toner particles were crushed. Further, fine particles generated at that time caused fog after 10,000 copies.
【0052】[0052]
【発明の効果】本発明の方法によれば、画像形成に用い
るトナー粒子について、形状係数Sの個数分布を特定の
範囲に規定しているので、トナーの粒子形状に起因する
クリーニング不良や画像濃度の低下を発生させることな
く、また、トナー粒子の帯電分布もシャープとなってカ
ブリ等の画像不良を発生させない。According to the method of the present invention, with respect to the toner particles used for image formation, the number distribution of the shape factor S is regulated within a specific range. Therefore, cleaning failure and image density due to the toner particle shape are caused. Does not occur, and the charge distribution of the toner particles becomes sharp, and image defects such as fog do not occur.
【図1】本発明に使用することができる像形成装置の一
例を示す概略説明図である。FIG. 1 is a schematic explanatory view showing an example of an image forming apparatus that can be used in the present invention.
【図2】像形成装置に搭載される非接触現像装置の構成
を示す概略説明図である。FIG. 2 is a schematic explanatory diagram showing a configuration of a non-contact developing device mounted on the image forming apparatus.
10 原稿台 11 照明光源 12 ミラー 12 レンズ 14 像形成体 15 露光ランプ 16 転写極 17 分離極 20 現像剤搬送担持体 21 磁石ロール 22 現像スリーブ 23 現像剤量規
制体 24 交流バイアス電源 25 攪拌装置 26 攪拌装置 27 トナー補給
ローラ 28 トナーホッパ 31 定着器 32 除電極 33 クリーニン
グ装置 34 ブレード 36 ローラ10 Document Plate 11 Illumination Light Source 12 Mirror 12 Lens 14 Image Forming Body 15 Exposure Lamp 16 Transfer Electrode 17 Separation Electrode 20 Developer Conveying Carrier 21 Magnet Roll 22 Developing Sleeve 23 Developer Amount Regulator 24 AC Bias Power Supply 25 Stirrer 26 Stirrer Device 27 Toner supply roller 28 Toner hopper 31 Fixing device 32 Eliminating electrode 33 Cleaning device 34 Blade 36 Roller
───────────────────────────────────────────────────── フロントページの続き (72)発明者 田中 真由美 東京都八王子市石川町2970番地コニカ株式 会社内 ─────────────────────────────────────────────────── ─── Continuation of the front page (72) Inventor Mayumi Tanaka 2970 Ishikawa-cho, Hachioji-shi, Tokyo Konica Stock Company
Claims (3)
って像形成体上の転写残留トナーを除去する工程を含む
画像形成方法において、 この画像形成方法に用いる現像剤を構成するトナーが下
記の条件を満たすことを特徴とする画像形成方法。 <条件>形状係数Sを、S=(周長)2 /(面積×4
π)×100と定義するときに、 S<116となるトナー粒子のトナー粒子全体に対
する個数比率Aが30%以下であること S>145となるトナー粒子のトナー粒子全体に対
する個数比率Bが30%以下であること 個数比率Aと個数比率Bとの合計が40%以下であ
ること1. An image forming method including a step of removing transfer residual toner on an image forming body by a cleaning device equipped with a blade, wherein a toner constituting a developer used in this image forming method satisfies the following conditions. And an image forming method. <Condition> The shape factor S is S = (perimeter) 2 / (area × 4)
π) × 100, the number ratio A of toner particles satisfying S <116 to the entire toner particles is 30% or less, and the number ratio B of toner particles satisfying S> 145 to the entire toner particles is 30%. The total of the number ratio A and the number ratio B is 40% or less
によって現像剤搬送担持体上に付着した現像剤を薄層化
し、この現像剤の薄層を、像形成体に対して非接触とな
る状態で現像領域に搬送し、前記現像剤搬送担持体に交
流バイアス電圧を印加して得られる振動電界下で像形成
体上の静電潜像を現像する工程と、ブレードを備えたク
リーニング装置によって像形成体上の転写残留トナーを
除去する工程とを含む画像形成方法において、 この画像形成方法に用いる現像剤を構成するトナーが請
求項1に記載されたトナーであることを特徴とする画像
形成方法。2. A thin layer of the developer adhered on the developer transport carrier is utilized by utilizing the pressing force of the developer amount regulator, and the thin layer of the developer is not in contact with the image forming body. And a developing blade to develop the electrostatic latent image on the image forming body under an oscillating electric field obtained by applying an AC bias voltage to the developer carrying carrier, and cleaning with a blade. An image forming method including a step of removing transfer residual toner on an image forming body by an apparatus, wherein the toner constituting the developer used in this image forming method is the toner according to claim 1. Image forming method.
媒体中で重合反応させて得られる平均粒径0.1〜3μ
mの1次粒子が相互に会合してなる平均粒径2〜6μm
の2次粒子からなるトナーと、樹脂被覆キャリアとを混
合することにより製造される現像剤を用いることを特徴
とする請求項1または請求項2に記載の画像形成方法。3. An average particle size of 0.1 to 3 μm obtained by polymerizing a polymerizable composition containing a polymerizable monomer in an aqueous medium.
average particle diameter of 2 to 6 μm in which primary particles of m are associated with each other.
3. The image forming method according to claim 1 or 2, wherein a developer produced by mixing the toner composed of the secondary particles described above with a resin-coated carrier is used.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP4322266A JPH06148926A (en) | 1992-11-09 | 1992-11-09 | Method for forming image |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP4322266A JPH06148926A (en) | 1992-11-09 | 1992-11-09 | Method for forming image |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| JPH06148926A true JPH06148926A (en) | 1994-05-27 |
Family
ID=18141730
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP4322266A Withdrawn JPH06148926A (en) | 1992-11-09 | 1992-11-09 | Method for forming image |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPH06148926A (en) |
Cited By (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5935753A (en) * | 1997-08-21 | 1999-08-10 | Fuji Xerox Co., Ltd. | Toner and developer for electrostatic latent image development and image forming method using the same |
| JP2000284534A (en) * | 1999-04-01 | 2000-10-13 | Tomoegawa Paper Co Ltd | Electrostatic toner and method for producing the same |
| JP2002023408A (en) * | 2000-07-10 | 2002-01-23 | Konica Corp | Electrostatic latent image developing toner, method for image formation and device for image formation |
| US6393250B1 (en) * | 1996-11-29 | 2002-05-21 | Canon Kabushiki Kaisha | Cleaning apparatus and image forming apparatus |
| US8372569B2 (en) | 2006-11-17 | 2013-02-12 | Ricoh Company, Ltd. | Toner, and image forming method and process cartridge using the toner |
-
1992
- 1992-11-09 JP JP4322266A patent/JPH06148926A/en not_active Withdrawn
Cited By (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US6393250B1 (en) * | 1996-11-29 | 2002-05-21 | Canon Kabushiki Kaisha | Cleaning apparatus and image forming apparatus |
| US5935753A (en) * | 1997-08-21 | 1999-08-10 | Fuji Xerox Co., Ltd. | Toner and developer for electrostatic latent image development and image forming method using the same |
| JP2000284534A (en) * | 1999-04-01 | 2000-10-13 | Tomoegawa Paper Co Ltd | Electrostatic toner and method for producing the same |
| JP2002023408A (en) * | 2000-07-10 | 2002-01-23 | Konica Corp | Electrostatic latent image developing toner, method for image formation and device for image formation |
| US8372569B2 (en) | 2006-11-17 | 2013-02-12 | Ricoh Company, Ltd. | Toner, and image forming method and process cartridge using the toner |
| US9256147B2 (en) | 2006-11-17 | 2016-02-09 | Ricoh Company, Ltd. | Toner, and image forming method and process cartridge using the toner |
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| A300 | Withdrawal of application because of no request for examination |
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