JPH04338970A - Electrophotographic dry developer - Google Patents
Electrophotographic dry developerInfo
- Publication number
- JPH04338970A JPH04338970A JP3143314A JP14331491A JPH04338970A JP H04338970 A JPH04338970 A JP H04338970A JP 3143314 A JP3143314 A JP 3143314A JP 14331491 A JP14331491 A JP 14331491A JP H04338970 A JPH04338970 A JP H04338970A
- Authority
- JP
- Japan
- Prior art keywords
- toner
- fine powder
- developer
- weight
- toner particles
- 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
- 239000002245 particle Substances 0.000 claims abstract description 71
- 239000000843 powder Substances 0.000 claims abstract description 58
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims abstract description 34
- 239000010457 zeolite Substances 0.000 claims abstract description 19
- 229910021536 Zeolite Inorganic materials 0.000 claims abstract description 17
- HNPSIPDUKPIQMN-UHFFFAOYSA-N dioxosilane;oxo(oxoalumanyloxy)alumane Chemical compound O=[Si]=O.O=[Al]O[Al]=O HNPSIPDUKPIQMN-UHFFFAOYSA-N 0.000 claims abstract description 17
- 229920005989 resin Polymers 0.000 claims abstract description 16
- 239000011347 resin Substances 0.000 claims abstract description 16
- 239000003086 colorant Substances 0.000 claims abstract description 10
- 239000011230 binding agent Substances 0.000 claims abstract description 7
- 239000003205 fragrance Substances 0.000 claims description 11
- 239000010419 fine particle Substances 0.000 claims description 4
- 239000002304 perfume Substances 0.000 abstract description 5
- 230000000052 comparative effect Effects 0.000 description 38
- 238000012360 testing method Methods 0.000 description 27
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 26
- 238000000034 method Methods 0.000 description 25
- 229920001577 copolymer Polymers 0.000 description 20
- 235000019645 odor Nutrition 0.000 description 13
- SESFRYSPDFLNCH-UHFFFAOYSA-N benzyl benzoate Chemical compound C=1C=CC=CC=1C(=O)OCC1=CC=CC=C1 SESFRYSPDFLNCH-UHFFFAOYSA-N 0.000 description 12
- 229910052681 coesite Inorganic materials 0.000 description 12
- 229910052906 cristobalite Inorganic materials 0.000 description 12
- 230000001953 sensory effect Effects 0.000 description 12
- 239000000377 silicon dioxide Substances 0.000 description 12
- 235000012239 silicon dioxide Nutrition 0.000 description 12
- 229910052682 stishovite Inorganic materials 0.000 description 12
- 229910052905 tridymite Inorganic materials 0.000 description 12
- FUJCRWPEOMXPAD-UHFFFAOYSA-N Li2O Inorganic materials [Li+].[Li+].[O-2] FUJCRWPEOMXPAD-UHFFFAOYSA-N 0.000 description 11
- XUCJHNOBJLKZNU-UHFFFAOYSA-M dilithium;hydroxide Chemical compound [Li+].[Li+].[OH-] XUCJHNOBJLKZNU-UHFFFAOYSA-M 0.000 description 11
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 10
- 229910052593 corundum Inorganic materials 0.000 description 10
- 239000000126 substance Substances 0.000 description 10
- 229910001845 yogo sapphire Inorganic materials 0.000 description 10
- 229910000859 α-Fe Inorganic materials 0.000 description 10
- NOOLISFMXDJSKH-KXUCPTDWSA-N (-)-Menthol Chemical compound CC(C)[C@@H]1CC[C@@H](C)C[C@H]1O NOOLISFMXDJSKH-KXUCPTDWSA-N 0.000 description 7
- -1 chloropolystyrene Polymers 0.000 description 7
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 6
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 6
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 6
- 229960002903 benzyl benzoate Drugs 0.000 description 6
- 238000010438 heat treatment Methods 0.000 description 6
- TWNQGVIAIRXVLR-UHFFFAOYSA-N oxo(oxoalumanyloxy)alumane Chemical compound O=[Al]O[Al]=O TWNQGVIAIRXVLR-UHFFFAOYSA-N 0.000 description 6
- OGIDPMRJRNCKJF-UHFFFAOYSA-N titanium oxide Inorganic materials [Ti]=O OGIDPMRJRNCKJF-UHFFFAOYSA-N 0.000 description 6
- NOOLISFMXDJSKH-UHFFFAOYSA-N DL-menthol Natural products CC(C)C1CCC(C)CC1O NOOLISFMXDJSKH-UHFFFAOYSA-N 0.000 description 5
- 239000006229 carbon black Substances 0.000 description 5
- 238000002156 mixing Methods 0.000 description 5
- BYFGZMCJNACEKR-UHFFFAOYSA-N aluminium(i) oxide Chemical compound [Al]O[Al] BYFGZMCJNACEKR-UHFFFAOYSA-N 0.000 description 4
- 239000000975 dye Substances 0.000 description 4
- RRAFCDWBNXTKKO-UHFFFAOYSA-N eugenol Chemical compound COC1=CC(CC=C)=CC=C1O RRAFCDWBNXTKKO-UHFFFAOYSA-N 0.000 description 4
- 239000000203 mixture Substances 0.000 description 4
- 241000220317 Rosa Species 0.000 description 3
- 238000011161 development Methods 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- 238000009472 formulation Methods 0.000 description 3
- 239000000178 monomer Substances 0.000 description 3
- SATCULPHIDQDRE-UHFFFAOYSA-N piperonal Chemical compound O=CC1=CC=C2OCOC2=C1 SATCULPHIDQDRE-UHFFFAOYSA-N 0.000 description 3
- 239000011164 primary particle Substances 0.000 description 3
- 229920005992 thermoplastic resin Polymers 0.000 description 3
- OOCCDEMITAIZTP-QPJJXVBHSA-N (E)-cinnamyl alcohol Chemical compound OC\C=C\C1=CC=CC=C1 OOCCDEMITAIZTP-QPJJXVBHSA-N 0.000 description 2
- FKUPPRZPSYCDRS-UHFFFAOYSA-N Cyclopentadecanolide Chemical compound O=C1CCCCCCCCCCCCCCO1 FKUPPRZPSYCDRS-UHFFFAOYSA-N 0.000 description 2
- GLZPCOQZEFWAFX-UHFFFAOYSA-N Geraniol Chemical compound CC(C)=CCCC(C)=CCO GLZPCOQZEFWAFX-UHFFFAOYSA-N 0.000 description 2
- PMGCQNGBLMMXEW-UHFFFAOYSA-N Isoamyl salicylate Chemical compound CC(C)CCOC(=O)C1=CC=CC=C1O PMGCQNGBLMMXEW-UHFFFAOYSA-N 0.000 description 2
- 241000234435 Lilium Species 0.000 description 2
- 239000004743 Polypropylene Substances 0.000 description 2
- 239000004793 Polystyrene Substances 0.000 description 2
- 230000004913 activation Effects 0.000 description 2
- IGODOXYLBBXFDW-UHFFFAOYSA-N alpha-Terpinyl acetate Chemical compound CC(=O)OC(C)(C)C1CCC(C)=CC1 IGODOXYLBBXFDW-UHFFFAOYSA-N 0.000 description 2
- USIUVYZYUHIAEV-UHFFFAOYSA-N diphenyl ether Chemical compound C=1C=CC=CC=1OC1=CC=CC=C1 USIUVYZYUHIAEV-UHFFFAOYSA-N 0.000 description 2
- 235000013399 edible fruits Nutrition 0.000 description 2
- 238000004898 kneading Methods 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- GVOWHGSUZUUUDR-UHFFFAOYSA-N methyl N-methylanthranilate Chemical compound CNC1=CC=CC=C1C(=O)OC GVOWHGSUZUUUDR-UHFFFAOYSA-N 0.000 description 2
- ZRSNZINYAWTAHE-UHFFFAOYSA-N p-methoxybenzaldehyde Chemical compound COC1=CC=C(C=O)C=C1 ZRSNZINYAWTAHE-UHFFFAOYSA-N 0.000 description 2
- 229920001155 polypropylene Polymers 0.000 description 2
- 229920002223 polystyrene Polymers 0.000 description 2
- 239000011148 porous material Substances 0.000 description 2
- XLOMVQKBTHCTTD-UHFFFAOYSA-N zinc oxide Inorganic materials [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 description 2
- SDOFMBGMRVAJNF-KVTDHHQDSA-N (2r,3r,4r,5r)-6-aminohexane-1,2,3,4,5-pentol Chemical compound NC[C@@H](O)[C@@H](O)[C@H](O)[C@H](O)CO SDOFMBGMRVAJNF-KVTDHHQDSA-N 0.000 description 1
- OFHHDSQXFXLTKC-UHFFFAOYSA-N 10-undecenal Chemical compound C=CCCCCCCCCC=O OFHHDSQXFXLTKC-UHFFFAOYSA-N 0.000 description 1
- DNRJTBAOUJJKDY-UHFFFAOYSA-N 2-Acetyl-3,5,5,6,8,8-hexamethyl-5,6,7,8- tetrahydronaphthalene Chemical compound CC(=O)C1=C(C)C=C2C(C)(C)C(C)CC(C)(C)C2=C1 DNRJTBAOUJJKDY-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
- FLUWAIIVLCVEKF-UHFFFAOYSA-N 2-Methyl-1-phenyl-2-propanyl acetate Chemical compound CC(=O)OC(C)(C)CC1=CC=CC=C1 FLUWAIIVLCVEKF-UHFFFAOYSA-N 0.000 description 1
- ACYXOHNDKRVKLH-UHFFFAOYSA-N 5-phenylpenta-2,4-dienenitrile prop-2-enoic acid Chemical compound OC(=O)C=C.N#CC=CC=CC1=CC=CC=C1 ACYXOHNDKRVKLH-UHFFFAOYSA-N 0.000 description 1
- 229910002012 Aerosil® Inorganic materials 0.000 description 1
- 238000004438 BET method Methods 0.000 description 1
- 239000005973 Carvone Substances 0.000 description 1
- NPBVQXIMTZKSBA-UHFFFAOYSA-N Chavibetol Natural products COC1=CC=C(CC=C)C=C1O NPBVQXIMTZKSBA-UHFFFAOYSA-N 0.000 description 1
- WTEVQBCEXWBHNA-UHFFFAOYSA-N Citral Natural products CC(C)=CCCC(C)=CC=O WTEVQBCEXWBHNA-UHFFFAOYSA-N 0.000 description 1
- 241000207199 Citrus Species 0.000 description 1
- 235000005979 Citrus limon Nutrition 0.000 description 1
- 244000131522 Citrus pyriformis Species 0.000 description 1
- 244000060011 Cocos nucifera Species 0.000 description 1
- 235000013162 Cocos nucifera Nutrition 0.000 description 1
- 241000612152 Cyclamen hederifolium Species 0.000 description 1
- 239000005770 Eugenol Substances 0.000 description 1
- 239000005792 Geraniol Substances 0.000 description 1
- GLZPCOQZEFWAFX-YFHOEESVSA-N Geraniol Natural products CC(C)=CCC\C(C)=C/CO GLZPCOQZEFWAFX-YFHOEESVSA-N 0.000 description 1
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 1
- 244000178870 Lavandula angustifolia Species 0.000 description 1
- 235000010663 Lavandula angustifolia Nutrition 0.000 description 1
- 229920001890 Novodur Polymers 0.000 description 1
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 1
- 239000004698 Polyethylene Substances 0.000 description 1
- UVMRYBDEERADNV-UHFFFAOYSA-N Pseudoeugenol Natural products COC1=CC(C(C)=C)=CC=C1O UVMRYBDEERADNV-UHFFFAOYSA-N 0.000 description 1
- 229910052581 Si3N4 Inorganic materials 0.000 description 1
- 229920007962 Styrene Methyl Methacrylate Polymers 0.000 description 1
- 244000297179 Syringa vulgaris Species 0.000 description 1
- 235000004338 Syringa vulgaris Nutrition 0.000 description 1
- 229910007541 Zn O Inorganic materials 0.000 description 1
- 230000003213 activating effect Effects 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 239000000853 adhesive Substances 0.000 description 1
- 230000001070 adhesive effect Effects 0.000 description 1
- 239000012790 adhesive layer Substances 0.000 description 1
- 230000002411 adverse Effects 0.000 description 1
- 150000001299 aldehydes Chemical class 0.000 description 1
- OOCCDEMITAIZTP-UHFFFAOYSA-N allylic benzylic alcohol Natural products OCC=CC1=CC=CC=C1 OOCCDEMITAIZTP-UHFFFAOYSA-N 0.000 description 1
- SOGAXMICEFXMKE-UHFFFAOYSA-N alpha-Methyl-n-butyl acrylate Natural products CCCCOC(=O)C(C)=C SOGAXMICEFXMKE-UHFFFAOYSA-N 0.000 description 1
- 239000012298 atmosphere Substances 0.000 description 1
- IRERQBUNZFJFGC-UHFFFAOYSA-L azure blue Chemical compound [Na+].[Na+].[Na+].[Na+].[Na+].[Na+].[Na+].[Na+].[Al+3].[Al+3].[Al+3].[Al+3].[Al+3].[Al+3].[S-]S[S-].[O-][Si]([O-])([O-])[O-].[O-][Si]([O-])([O-])[O-].[O-][Si]([O-])([O-])[O-].[O-][Si]([O-])([O-])[O-].[O-][Si]([O-])([O-])[O-].[O-][Si]([O-])([O-])[O-] IRERQBUNZFJFGC-UHFFFAOYSA-L 0.000 description 1
- JRPBQTZRNDNNOP-UHFFFAOYSA-N barium titanate Chemical compound [Ba+2].[Ba+2].[O-][Ti]([O-])([O-])[O-] JRPBQTZRNDNNOP-UHFFFAOYSA-N 0.000 description 1
- 229910002113 barium titanate Inorganic materials 0.000 description 1
- 239000011324 bead Substances 0.000 description 1
- 210000000988 bone and bone Anatomy 0.000 description 1
- 238000012662 bulk polymerization Methods 0.000 description 1
- 239000012876 carrier material Substances 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- WJSDHUCWMSHDCR-VMPITWQZSA-N cinnamyl acetate Natural products CC(=O)OC\C=C\C1=CC=CC=C1 WJSDHUCWMSHDCR-VMPITWQZSA-N 0.000 description 1
- 229940043350 citral Drugs 0.000 description 1
- 235000020971 citrus fruits Nutrition 0.000 description 1
- 239000003245 coal Substances 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- XCJYREBRNVKWGJ-UHFFFAOYSA-N copper(II) phthalocyanine Chemical compound [Cu+2].C12=CC=CC=C2C(N=C2[N-]C(C3=CC=CC=C32)=N2)=NC1=NC([C]1C=CC=CC1=1)=NC=1N=C1[C]3C=CC=CC3=C2[N-]1 XCJYREBRNVKWGJ-UHFFFAOYSA-N 0.000 description 1
- 239000013078 crystal Substances 0.000 description 1
- 229930186364 cyclamen Natural products 0.000 description 1
- 229940019836 cyclamen aldehyde Drugs 0.000 description 1
- 230000001877 deodorizing effect Effects 0.000 description 1
- 229940095104 dimethyl benzyl carbinyl acetate Drugs 0.000 description 1
- 230000005611 electricity Effects 0.000 description 1
- 238000007720 emulsion polymerization reaction Methods 0.000 description 1
- 239000003822 epoxy resin Substances 0.000 description 1
- 229920006244 ethylene-ethyl acrylate Polymers 0.000 description 1
- 229960002217 eugenol Drugs 0.000 description 1
- 238000001704 evaporation Methods 0.000 description 1
- 238000010528 free radical solution polymerization reaction Methods 0.000 description 1
- 238000007429 general method Methods 0.000 description 1
- WTEVQBCEXWBHNA-JXMROGBWSA-N geranial Chemical compound CC(C)=CCC\C(C)=C\C=O WTEVQBCEXWBHNA-JXMROGBWSA-N 0.000 description 1
- HIGQPQRQIQDZMP-UHFFFAOYSA-N geranil acetate Natural products CC(C)=CCCC(C)=CCOC(C)=O HIGQPQRQIQDZMP-UHFFFAOYSA-N 0.000 description 1
- 229940113087 geraniol Drugs 0.000 description 1
- HIGQPQRQIQDZMP-DHZHZOJOSA-N geranyl acetate Chemical compound CC(C)=CCC\C(C)=C\COC(C)=O HIGQPQRQIQDZMP-DHZHZOJOSA-N 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 230000007062 hydrolysis Effects 0.000 description 1
- 238000006460 hydrolysis reaction Methods 0.000 description 1
- 229910052500 inorganic mineral Inorganic materials 0.000 description 1
- 229920000554 ionomer Polymers 0.000 description 1
- 125000001972 isopentyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])C([H])([H])* 0.000 description 1
- 150000002576 ketones Chemical class 0.000 description 1
- 239000001102 lavandula vera Substances 0.000 description 1
- 235000018219 lavender Nutrition 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
- 229940107698 malachite green Drugs 0.000 description 1
- FDZZZRQASAIRJF-UHFFFAOYSA-M malachite green Chemical compound [Cl-].C1=CC(N(C)C)=CC=C1C(C=1C=CC=CC=1)=C1C=CC(=[N+](C)C)C=C1 FDZZZRQASAIRJF-UHFFFAOYSA-M 0.000 description 1
- 150000002689 maleic acids Chemical class 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 239000001683 mentha spicata herb oil Substances 0.000 description 1
- 229910021645 metal ion Inorganic materials 0.000 description 1
- 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 1
- 239000011707 mineral Substances 0.000 description 1
- 239000000025 natural resin Substances 0.000 description 1
- 230000009965 odorless effect Effects 0.000 description 1
- 230000003287 optical effect Effects 0.000 description 1
- 230000001590 oxidative effect Effects 0.000 description 1
- CSZZVSAEGFJSQO-UHFFFAOYSA-N phenyl 2-methylprop-2-enoate;styrene Chemical compound C=CC1=CC=CC=C1.CC(=C)C(=O)OC1=CC=CC=C1 CSZZVSAEGFJSQO-UHFFFAOYSA-N 0.000 description 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
- 108091008695 photoreceptors Proteins 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 229940081310 piperonal Drugs 0.000 description 1
- 229920002037 poly(vinyl butyral) polymer Polymers 0.000 description 1
- 229920000647 polyepoxide Polymers 0.000 description 1
- 229920001225 polyester resin Polymers 0.000 description 1
- 239000004645 polyester resin Substances 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 238000006116 polymerization reaction Methods 0.000 description 1
- 229920005749 polyurethane resin Polymers 0.000 description 1
- 238000010298 pulverizing process Methods 0.000 description 1
- 150000003242 quaternary ammonium salts Chemical class 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 229930187593 rose bengal Natural products 0.000 description 1
- AZJPTIGZZTZIDR-UHFFFAOYSA-L rose bengal Chemical compound [K+].[K+].[O-]C(=O)C1=C(Cl)C(Cl)=C(Cl)C(Cl)=C1C1=C2C=C(I)C(=O)C(I)=C2OC2=C(I)C([O-])=C(I)C=C21 AZJPTIGZZTZIDR-UHFFFAOYSA-L 0.000 description 1
- 229940081623 rose bengal Drugs 0.000 description 1
- STRXNPAVPKGJQR-UHFFFAOYSA-N rose bengal A Natural products O1C(=O)C(C(=CC=C2Cl)Cl)=C2C21C1=CC(I)=C(O)C(I)=C1OC1=C(I)C(O)=C(I)C=C21 STRXNPAVPKGJQR-UHFFFAOYSA-N 0.000 description 1
- 238000007789 sealing 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
- HQVNEWCFYHHQES-UHFFFAOYSA-N silicon nitride Chemical compound N12[Si]34N5[Si]62N3[Si]51N64 HQVNEWCFYHHQES-UHFFFAOYSA-N 0.000 description 1
- 229910052814 silicon oxide Inorganic materials 0.000 description 1
- 229920002050 silicone resin Polymers 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 235000019721 spearmint oil Nutrition 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 229920003048 styrene butadiene rubber Polymers 0.000 description 1
- 238000010557 suspension polymerization reaction Methods 0.000 description 1
- 229920003002 synthetic resin Polymers 0.000 description 1
- 239000000057 synthetic resin Substances 0.000 description 1
- 235000013799 ultramarine blue Nutrition 0.000 description 1
- 229920006337 unsaturated polyester resin Polymers 0.000 description 1
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
- 229920002554 vinyl polymer Polymers 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 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
- 239000002023 wood Substances 0.000 description 1
- ZFNVDHOSLNRHNN-UHFFFAOYSA-N xi-3-(4-Isopropylphenyl)-2-methylpropanal Chemical compound O=CC(C)CC1=CC=C(C(C)C)C=C1 ZFNVDHOSLNRHNN-UHFFFAOYSA-N 0.000 description 1
- 239000008096 xylene Substances 0.000 description 1
Abstract
Description
【0001】0001
【産業上の利用分野】本発明は、電子写真乾式現像剤の
改良に関する。FIELD OF THE INVENTION This invention relates to improvements in electrophotographic dry developers.
【0002】0002
【従来の技術】従来電子写真法としては米国特許第22
97691号明細書、特公昭49−23910号公報及
び特公昭43−24748号公報等に各種の方法が記載
されているが、一般には光導電性物質を利用し、種々の
手段により感光体に電気的潜像を形成し、次いで該潜像
をトナーを用いて現像し、必要に応じて紙等に粉像を転
写した後、加熱あるいは溶剤蒸気等により定着しコピー
を得るものである。[Prior Art] As a conventional electrophotographic method, US Pat.
Various methods are described in Japanese Patent Publication No. 97691, Japanese Patent Publication No. 49-23910, Japanese Patent Publication No. 43-24748, etc., but generally a photoconductive substance is used and electricity is applied to the photoreceptor by various means. This process forms a latent image, then develops the latent image using toner, transfers the powder image to paper or the like as required, and then fixes it by heating or solvent vapor to obtain a copy.
【0003】電気的潜像を現像する方式には大別して絶
縁性有機液体中に各種の顔料や染料を微細に分散させた
現像剤を用いる液体現像方式とカスケード法、磁気ブラ
シ法、パウダークラウド法等のように天然又は合成樹脂
にカーボンブラック等の着色剤を分散せしめたトナーを
用いる所謂乾式現像方式とがあり、更にトナーのみから
なる一成分系現像剤と、トナーと、鉄粉、フェライト、
ガラスビーズ等の担体物質とを併用する二成分系現像剤
に分けられる。[0003] Methods for developing electrical latent images are broadly divided into liquid development methods using a developer in which various pigments and dyes are finely dispersed in an insulating organic liquid, cascade methods, magnetic brush methods, and powder cloud methods. There is a so-called dry development method that uses toner in which a colorant such as carbon black is dispersed in natural or synthetic resin, and there is also a one-component developer consisting only of toner, toner, iron powder, ferrite, etc.
It is divided into two-component developers that are used in combination with carrier materials such as glass beads.
【0004】一般的な乾式現像用トナーの製造方法とし
ては、熱可塑性樹脂、着色剤、荷電制御剤、その他必要
に応じて添加剤等を予備混合し、この混合物を加熱ロー
ル、加熱ニーダー、エクストルーダー等により溶融混練
し、得られた塊状物をジェットミル、I式ミル等の機械
的粉砕手段により粉砕し、その後分級して所望の粒径を
有するトナーを製造していた。[0004] A general method for manufacturing toner for dry development involves premixing a thermoplastic resin, a colorant, a charge control agent, and other additives as necessary, and then applying this mixture to a heating roll, a heating kneader, or an extruder. The resulting agglomerates are melted and kneaded using a ruder or the like, and the resulting agglomerates are pulverized using a mechanical pulverizing means such as a jet mill or an I-type mill, and then classified to produce toner having a desired particle size.
【0005】しかし、これらの従来技術によって製造さ
れたトナーには以下に述べるような問題点がある。However, the toners produced by these conventional techniques have the following problems.
【0006】まず、トナーの主原料である熱可塑性樹脂
は重合によって得られる高分子量物質が主であるため残
存モノマーが存在する。First, since the thermoplastic resin, which is the main raw material of the toner, is mainly a high molecular weight substance obtained by polymerization, residual monomers exist.
【0007】この残存モノマーは特に結着樹脂として広
く一般的に使用されているビニル系高分子の場合、悪臭
が著しい。又、残存モノマーの量がごく微量でも定着に
よる加熱時には悪臭が発生する。[0007] This residual monomer has a significant odor, especially in the case of vinyl polymers which are widely and generally used as binder resins. Further, even if the amount of residual monomer is extremely small, a bad odor is generated during heating during fixing.
【0008】この加熱による悪臭の発生は定着時だけで
はなく、これらのトナーを補給用として複写機内に入れ
ておいた場合、光学系や定着部の発熱により複写機内の
温度が上昇することによっても発生する。[0008] The occurrence of bad odor due to this heating occurs not only during fixing, but also when the toner is stored in the copying machine for replenishment, the temperature inside the copying machine rises due to the heat generated by the optical system and fixing section. Occur.
【0009】これらの欠点を解決するため下記に示すよ
うに種々の提案がなされている。[0009] In order to solve these drawbacks, various proposals have been made as shown below.
【0010】(1)特開昭48−65945号公報では
トナー中に香料を添加後混練する方法が、(2)特開昭
52−113737号公報では、香料の微粉末をトナー
中に混合し、トナー表面にこれを保持する方法が、(3
)特開昭62−141567号公報ではマイクロカプセ
ル化した香料をトナーに添加する方法が、(4)特開昭
62−210474号ではトナー中に香料を封止する方
法が、それぞれ提案されている。(1) Japanese Patent Application Laid-Open No. 48-65945 discloses a method in which a fragrance is added to the toner and then kneaded. (2) Japanese Patent Application Laid-Open No. 52-113737 discloses a method in which a fine powder of a fragrance is mixed into a toner. , the method of holding this on the toner surface is (3
) JP-A No. 62-141567 proposes a method of adding a micro-encapsulated fragrance to a toner, and (4) JP-A No. 62-210474 proposes a method of sealing a fragrance in a toner. .
【0011】(1)の方法では、一般的に香料は化学構
造的に非常に不安定であり、混練時の撹拌や熱により、
分解又は蒸発してしまい満足する効果は得られない。こ
れを解決するために提案されたのが(2)の方法である
が、例えば二成分現像剤として使用した場合、香料微粉
末がキャリア側へ移行してしまい、充分な効果が期待で
きない。又、(3)(4)は共に定着時の圧力や熱によ
り、香料が外部に飛び出し、効果が出るようになってい
るが、複写気内の温度上昇などにより発生する悪臭に対
する効果はない。[0011] In the method (1), fragrances are generally very unstable chemically, so stirring and heat during kneading may cause
It decomposes or evaporates, and a satisfactory effect cannot be obtained. Method (2) has been proposed to solve this problem, but when used, for example, as a two-component developer, the perfume fine powder migrates to the carrier side, and a sufficient effect cannot be expected. In addition, (3) and (4) are both effective because the fragrance is ejected to the outside by the pressure and heat during fixing, but they are not effective against bad odors generated due to temperature rise in the copying atmosphere.
【0012】本発明はこれらの問題点を解決しようとす
るもので、その目的は複写機内や定着時において悪臭の
発生しない電子写真用乾式現像剤を提供することにある
。The present invention aims to solve these problems, and its purpose is to provide a dry developer for electrophotography that does not generate bad odor in a copying machine or during fixing.
【0013】[0013]
【課題を解決するための手段】本発明は結着樹脂および
着色剤を主成分とするトナー粒子と、香料により、その
表面を処理された微粉末とを含有したことを特徴とする
電子写真乾式現像剤である。[Means for Solving the Problems] The present invention provides an electrophotographic dry method characterized by containing toner particles whose main components are a binder resin and a colorant, and a fine powder whose surface is treated with a fragrance. It is a developer.
【0014】本発明は又、結着樹脂および着色剤を主成
分とするトナー粒子と活性炭、無機質ゲルおよびゼオラ
イトから選択された微粉末を含有したことを特徴とする
電子写真乾式現像剤である。The present invention also provides an electrophotographic dry developer characterized in that it contains toner particles containing a binder resin and a colorant as main components, and a fine powder selected from activated carbon, inorganic gel, and zeolite.
【0015】トナー粒子と上記各微粉末とは予め混合し
ておくことがよいが、トナー粒子表面に微粉末を固着せ
しめることもよい。固着の例としては、母体粒子の表面
に接着剤を介して微粉末が接着されているもの、あるい
はトナー表面に微粉末の一部を埋設しているもの等が挙
げられる。固着せしめる方法としては、トナー母体粒子
表面に薄い接着層を設け、これに微粉末を接着せしめる
方法、あるいは母体粒子の表面に微粉末を強い力で、例
えば、機械的な衝撃力で押し込む方法等がある。製造性
及びトナーとしての特性上後者の方法を採用することが
好ましい。It is preferable to mix the toner particles and each of the above-mentioned fine powders in advance, but it is also preferable to have the fine powders adhere to the surface of the toner particles. Examples of adhesion include those in which the fine powder is adhered to the surface of the base particle via an adhesive, or those in which a part of the fine powder is embedded in the toner surface. The fixing method includes a method of providing a thin adhesive layer on the surface of the toner base particles and adhering the fine powder to this, or a method of pushing the fine powder onto the surface of the base particles with strong force, such as mechanical impact force. There is. It is preferable to employ the latter method in terms of manufacturability and toner properties.
【0016】本発明に使用される結着樹脂の例としては
、例えば、ポリスチレン、クロロポリスチレン、ポリ−
α−スチルスチレン、スチレン−クロロスチレン共重合
体、スチレン−プロピレン共重合体、スチレン−ブタジ
エン共重合体、スチレン−塩化ビニル共重合体、スチレ
ン−酢酸ビニル共重合体、スチレン−マレイン酸共重合
体、スチレン−アクリル酸エステル共重合体、(スチレ
ン−アクリル酸メチル共重合体、スチレン−アクリル酸
エチル共重合体、スチレン−アクリル酸ブチル共重合体
、スチレン−アクリル酸オクチル共重合体、スチレン−
アクリル酸フェニル共重合体等)、スチレン−メタクリ
ル酸エステル共重合体(スチレン−メタクリル酸メチル
共重合体、スチレン−メタクリル酸エチル共重合体、ス
チレン−メタクリル酸ブチル共重合体、スチレン−メタ
クリル酸フェニル共重合体)、スチレン−α−クロルア
クリル酸メチル共重合体、スチレン−アクリロニトリル
−アクリル酸エステル共重合体等のスチレン系樹脂(ス
チレン又はスチレン置換体を含む単重合体又は共重合体
)、塩化ビニル樹脂、スチレン−酢酸ビニル共重合体、
ロジン変性マレイン酸樹脂、フェニール樹脂、エポキシ
樹脂、ポリエステル樹脂、低分子量ポリエチレン、低分
子量ポリプロピレン、アイオノマー樹脂、ポリウレタン
樹脂、シリコーン樹脂、ケトン樹脂、エチレン−エチル
アクリレート共重合体、キシレン樹脂、ポリビニルブチ
ラール樹脂等があるが、これらの樹脂は単独使用に限ら
ず、二種以上併用することもできる。Examples of the binder resin used in the present invention include polystyrene, chloropolystyrene, and polystyrene.
α-Stylstyrene, styrene-chlorostyrene copolymer, styrene-propylene copolymer, styrene-butadiene copolymer, styrene-vinyl chloride copolymer, styrene-vinyl acetate copolymer, styrene-maleic acid copolymer , styrene-acrylate copolymer, (styrene-methyl acrylate copolymer, styrene-ethyl acrylate copolymer, styrene-butyl acrylate copolymer, styrene-octyl acrylate copolymer, styrene-
(phenyl acrylate copolymer, etc.), styrene-methacrylate ester copolymer (styrene-methyl methacrylate copolymer, styrene-ethyl methacrylate copolymer, styrene-butyl methacrylate copolymer, styrene-phenyl methacrylate) styrenic resins (unipolymers or copolymers containing styrene or styrene substitutes), styrene-α-methyl chloroacrylate copolymers, styrene-acrylonitrile-acrylic acid ester copolymers, chlorinated Vinyl resin, styrene-vinyl acetate copolymer,
Rosin-modified maleic acid resin, phenyl resin, epoxy resin, polyester resin, low molecular weight polyethylene, low molecular weight polypropylene, ionomer resin, polyurethane resin, silicone resin, ketone resin, ethylene-ethyl acrylate copolymer, xylene resin, polyvinyl butyral resin, etc. However, these resins are not limited to single use, but can also be used in combination of two or more types.
【0017】又、これらの製造方法も特に限定されるも
のではなく、塊状重合、溶液重合、乳化重合、懸濁重合
いずれも利用できる。[0017] The manufacturing method for these is also not particularly limited, and any of bulk polymerization, solution polymerization, emulsion polymerization, and suspension polymerization can be used.
【0018】本発明の母体トナー粒子は必要に応じて各
種着色剤を用いることができ、具体的にはカーボンブラ
ック、ニグロシン系染料、アニリンブルー、ウルトラマ
リンブルー、フタロシアニンブルー、クロムイエロー、
マラカイトグリーン、ローズベンガル等が単独又は混合
して使用できる。着色剤の添加量は樹脂成分 100重
量部に対し1〜30重量部、好ましくは5〜15重量部
である。[0018] The base toner particles of the present invention may contain various colorants as required, and specifically include carbon black, nigrosine dye, aniline blue, ultramarine blue, phthalocyanine blue, chrome yellow,
Malachite green, rose bengal, etc. can be used alone or in combination. The amount of the colorant added is 1 to 30 parts by weight, preferably 5 to 15 parts by weight, per 100 parts by weight of the resin component.
【0019】又、四三酸化鉄、フェライト粉末等の磁性
体を添加してもよい。Further, magnetic substances such as triiron tetroxide and ferrite powder may be added.
【0020】本発明の母体トナー粒子は公知の方法で得
られ、例えば熱可塑性樹脂、着色剤等をよく混合し、次
に加圧ニーダー、加熱二本ロール、エクストルーダー等
で混練し、その後冷却固化、粉砕、分級することにより
得られる。The base toner particles of the present invention are obtained by a known method, for example, by thoroughly mixing a thermoplastic resin, a colorant, etc., then kneading with a pressure kneader, heated twin rolls, extruder, etc., and then cooling. Obtained by solidifying, crushing, and classifying.
【0021】香料としては香気を発する物質は全て使用
できるが具体的には次のようなものがある。[0021] As the fragrance, any substance that emits an aroma can be used, but specifically, the following substances are available.
【0022】(1) 安息香酸ベンジル(ほとんど無臭
、多少バルサムよう)
(2) 桂皮アルコール=シンナミルアルコール(ヒヤ
シンスふう)
(3) シクロペンタデカノリド(じゃ香よう)(4)
ジフェニルエーテル(ゼラニウムよう、バラよう)(
5) トナリド(果実よう)
(6) β−ナフチルアルキルエーテル(果実よう)(1) Benzyl benzoate (almost odorless, somewhat balsam-like) (2) Cinnamyl alcohol (hyacinth-like) (3) Cyclopentadecanolide (jako-like) (4)
Diphenyl ether (geranium-like, rose-like) (
5) Tonalid (fruit-like) (6) β-naphthyl alkyl ether (fruit-like)
【
0023】[
0023
【化1】[Chemical formula 1]
【0024】(7) ヘリオトロピン=ピペロナール(
ヘルオトロープ花よう)
(8) N−メチルアントラニル酸メチル(果実よう)
(9) l−メントール(薄荷)
(10)サリチル酸イソアミル(蘭よう)(11)ゲラ
ニオール(ばらの花よう)(12)l−カルボン(スペ
アミント油よう)(13)ウンデシレンアルデヒド(ロ
ーズよう、シトラスよう)
(14)オイゲノール(丁字よう)
(15)イン吉草酸イソアミル(果実よう)(16)ア
ニスアルデヒド(山査子よう)(17)酢酸ゲラニル(
バラの花よう)(18)酢酸シンナミル(花のかおり)
(7) Heliotropin=piperonal (
Helotrope flower) (8) Methyl N-methylanthranilate (fruit)
(9) L-Menthol (10) Isoamyl salicylate (11) Geraniol (Rose) (12) L-Carvone (Spearmint oil) (13) Undecylenaldehyde (Rose, Citrus) ) (14) Eugenol (15) Isoamyl invalerate (fruit) (16) Anisaldehyde (Yamasako) (17) Geranyl acetate (
(rose scent) (18) Cinnamyl acetate (flower scent)
【0025】[0025]
【化2】[Case 2]
【0026】(19)酢酸テルピニル(ラベンダーの花
よう)
(20)酢酸ジメチルベンジルカルビニル(ライラック
よう、リリーよう)
(21)p−t−ブチル−α−メチルハイドロシンナミ
ックアルデヒド(百合の花よう)
(22)シトラール(レモンよう)
(23)シクラメンアルデヒド(シクラメンよう)これ
らの物質は1種でも2種以上で用いられてもかまわない
。香料によって表面を処理される微粉末としては従来よ
り広く用いられている公知の材料が使用でき、例えば、
酸化ケイ素、酸化チタン、酸化アルミニウム、炭化ケイ
素、窒化ケイ素、チタン酸バリウム等が挙げられる。(19) Terpinyl acetate (like lavender) (20) Dimethylbenzylcarbinyl acetate (like lilac, like lily) (21) pt-butyl-α-methylhydrocinnamic aldehyde (like like lily) ) (22) Citral (like lemon) (23) Cyclamenaldehyde (like cyclamen) These substances may be used alone or in combination of two or more. As the fine powder whose surface is treated with perfume, known materials that have been widely used can be used, for example,
Examples include silicon oxide, titanium oxide, aluminum oxide, silicon carbide, silicon nitride, barium titanate, and the like.
【0027】微粉末の表面を香料によって処理する方法
は、アルコール等に香料を溶解し、それに微粉末を浸漬
後、アルコール等を蒸発させれば得られる。[0027] The surface of the fine powder can be treated with a perfume by dissolving the perfume in alcohol or the like, immersing the fine powder in it, and then evaporating the alcohol or the like.
【0028】母体トナー粒子に対するこれらの香料によ
り表面処理された微粉末の添加量は母体トナー粒子 1
00重量部に対して 0.1〜10.0重量部であり、
好ましくは 0.3〜3.0 重量部である。又、母体
トナー粒子とこれらの香料により表面処理された微粉末
との混合には各種ミキサーを用いることができる。The amount of the fine powder surface-treated with these fragrances added to the base toner particles is 1
0.1 to 10.0 parts by weight,
Preferably it is 0.3 to 3.0 parts by weight. Further, various mixers can be used to mix the base toner particles and the fine powder whose surface has been treated with these fragrances.
【0029】活性炭は、木材、ヤシガラ、パームカーネ
ルシェル、石炭、タール、骨、その他炭化する物質を賦
活(表面積を大きくする、すなわちミクロポアな部分を
多くする)することにより製造される。Activated carbon is produced by activating (increasing the surface area, ie, increasing the number of micropores) wood, coconut shell, palm kernel shell, coal, tar, bone, and other substances that can be carbonized.
【0030】活性炭の消臭機構は、賦活という操作によ
って生じたミクロポア部内に臭気物質が捕捉されること
であり、活性炭の性能はこの賦活という操作によって生
成するミクロポアの状態によって決まる。The deodorizing mechanism of activated carbon is that odor substances are trapped within the micropores created by the activation operation, and the performance of activated carbon is determined by the state of the micropores created by the activation operation.
【0031】活性炭の比表面積は500〜2000m2
/g(BET法)のものが使用できる。これらの活性炭
はジェット粉砕機などの粉砕機により微粉砕され、粒径
としては5.0μ以下、好ましくは0.01〜2.0μ
である。[0031] The specific surface area of activated carbon is 500 to 2000 m2
/g (BET method) can be used. These activated carbons are finely pulverized by a pulverizer such as a jet pulverizer, and the particle size is 5.0μ or less, preferably 0.01 to 2.0μ.
It is.
【0032】母体粒子に対する活性炭微粉末の添加量は
、母体粒子100重量部に対して0.1〜10.0重量
部であり、好ましくは0.3〜3.0重量部である。又
、母体粒子と活性炭微粉末との混合には各種ミキサーを
用いることができる。The amount of activated carbon fine powder added to the base particles is 0.1 to 10.0 parts by weight, preferably 0.3 to 3.0 parts by weight, per 100 parts by weight of the base particles. Moreover, various mixers can be used to mix the base particles and the activated carbon fine powder.
【0033】無機質ゲルとしては、SiO2・Al2O
3・ZnO・Li2O・Ag+の微粉末が用いられる。
このSiO2・Al2O3・ZnO・Li2O・Ag+
微粉末は加水分解法により製造された金属イオンを含有
する大表面積の微粒子であり、臭気に対して吸着と酸化
分解を同時に行い消臭する。[0033] As the inorganic gel, SiO2/Al2O
A fine powder of 3.ZnO.Li2O.Ag+ is used. This SiO2・Al2O3・ZnO・Li2O・Ag+
Fine powder is fine particles with a large surface area that contain metal ions produced by a hydrolysis method, and deodorizes odors by simultaneously adsorbing and oxidizing them.
【0034】SiO2・Al2O3・ZnO・Li2O
・Ag+の一次粒子の平均粒径は1.0μ以下が望まし
い。母体トナー粒子に対するSiO2・Al2O3・Z
nO・Li2O・Ag+微粉末の添加量は母体トナー粒
子100重量部に対し、0.1〜10.0重量部であり
、好ましくは、0.3〜5.0重量部である。これらの
粒子の混合には各種ミキサーを用いることができる。[0034]SiO2・Al2O3・ZnO・Li2O
- The average particle diameter of Ag+ primary particles is preferably 1.0 μm or less. SiO2・Al2O3・Z for base toner particles
The amount of nO.Li2O.Ag+fine powder added is 0.1 to 10.0 parts by weight, preferably 0.3 to 5.0 parts by weight, based on 100 parts by weight of the base toner particles. Various mixers can be used to mix these particles.
【0035】ゼオライトは、天然と合成があり、独特の
結晶構造により他の鉱物には見られない空洞と孔路を持
つ。通常この部分には多量の結晶水が含まれているが、
加熱、減圧により容易に除去でき、水の取れた状態のゼ
オライトは外部から孔路に入ってきた物質を吸着するこ
とができ、この機能が消臭の役割になる。これらゼオラ
イトはジェット粉砕機などの粉砕機により微粉砕され、
粒径としては5.0μ以下、好ましくは0.01〜2.
0μである。Zeolites come in both natural and synthetic forms, and have cavities and pores that are not found in other minerals due to their unique crystal structure. Normally, this part contains a large amount of crystallized water,
Zeolite can be easily removed by heating and depressurizing, and in its dehydrated state, zeolite can adsorb substances that enter its pores from the outside, and this function serves as a deodorizer. These zeolites are finely pulverized using a pulverizer such as a jet pulverizer.
The particle size is 5.0 μm or less, preferably 0.01 to 2.0 μm.
It is 0μ.
【0036】ゼオライト微粉末を母体粒子表面に固着す
る方法は、ゼオライト微粉末と母体粒子を回転体を備え
た密閉容器に入れ、高速回転による衝撃力や摩擦力など
の機械的衝撃エネルギーを与えることにより固着させる
方法などがある。母体粒子に対するゼオライト微粉末の
添加量は、母体粒子100重量部に対して0.1〜15
.0重量部であり、好ましくは0.5〜5.0重量部で
ある。[0036] The method of fixing the fine zeolite powder to the surface of the base particles is to place the fine zeolite powder and the base particles in an airtight container equipped with a rotating body, and apply mechanical impact energy such as impact force or friction force due to high-speed rotation. There are methods to make it stick. The amount of zeolite fine powder added to the base particles is 0.1 to 15 parts by weight per 100 parts by weight of the base particles.
.. 0 parts by weight, preferably 0.5 to 5.0 parts by weight.
【0037】[0037]
【実施例】次に実施例並びに比較例によって本発明を説
明する。[Examples] Next, the present invention will be explained with reference to Examples and Comparative Examples.
【0038】実施例1
スチレン−n−ブチルメタクリレート共重合体
88.0重量部 第4級アンモニウム塩
2.0重量部 カーボンブラック(#4
4:三菱化成製) 10.
0重量部 以上の処方でエクストルーダーを用いて混
練を行い、体積平均粒径10μの母体トナー粒子を得た
。Example 1 Styrene-n-butyl methacrylate copolymer
88.0 parts by weight Quaternary ammonium salt
2.0 parts by weight Carbon black (#4
4: Made by Mitsubishi Kasei) 10.
A formulation containing 0 parts by weight or more was kneaded using an extruder to obtain base toner particles having a volume average particle diameter of 10 μm.
【0039】次に安息香酸ベンジルの3%アルコール溶
液に酸化チタン(P−25:日本アエロジル)を浸漬後
アルコールを蒸発させ安息香酸ベンジルにより表面処理
された酸化チタン微粉末を得た。母体トナー粒子98重
量部に対し、表面処理された酸化チタン2重量部をミキ
サーにて混合し、本発明の現像剤(トナー)を得た。こ
のトナーを用いて現像剤を作成(キャリア:100μフ
ェライトキャリア)し、複写機(リコー社製FT−48
20)にて1000枚の連続コピーを行った。補給トナ
ーは300g複写機内にセットした。このとき20人の
モニターによる官能テストを行った。Next, titanium oxide (P-25: Nippon Aerosil) was immersed in a 3% alcohol solution of benzyl benzoate, and the alcohol was evaporated to obtain fine titanium oxide powder whose surface had been treated with benzyl benzoate. A developer (toner) of the present invention was obtained by mixing 2 parts by weight of surface-treated titanium oxide with 98 parts by weight of the base toner particles in a mixer. A developer was prepared using this toner (carrier: 100μ ferrite carrier), and a copying machine (FT-48 manufactured by Ricoh Co., Ltd.) was used.
20), 1000 sheets were continuously copied. 300 g of replenishment toner was set in the copying machine. At this time, a sensory test was conducted by 20 monitors.
【0040】比較例1
実施例1において、安息香酸ベンジルにより処理してい
ないP−25による現像剤(トナー)を作成して実施例
1と同様のテストを行った。Comparative Example 1 In Example 1, a developer (toner) using P-25 which was not treated with benzyl benzoate was prepared and the same test as in Example 1 was conducted.
【0041】結果をまとめて表1に示す。[0041] The results are summarized in Table 1.
【0042】なお、1000枚コピー後の画像は実施例
1、比較例1ともに差はなかった。Note that there was no difference in the images after copying 1000 sheets between Example 1 and Comparative Example 1.
【0043】[0043]
【表1】[Table 1]
【0044】実施例2
不飽和ポリエステル樹脂 88.0重量部ニ
グロシン染料 2.0重
量部カーボンブラック(#44) 10.0重量
部以上の処方でエクストルーダーを用いて混練を行い、
体積平均粒径10μの母体トナー粒子を得た。Example 2 Unsaturated polyester resin 88.0 parts by weight Nigrosine dye 2.0 parts by weight Carbon black (#44) 10.0 parts by weight or more was kneaded using an extruder.
Base toner particles having a volume average particle diameter of 10 μm were obtained.
【0045】次にl−メントールの 5%アルコール溶
液に酸化アルミニウム(メカノックスUB−10:上村
工業製)を浸漬後、アルコールを蒸発させl−メントー
ルにより表面処理された酸化アルミニウム微粉末を得た
。Next, aluminum oxide (Mechanox UB-10, manufactured by Uemura Industries) was immersed in a 5% alcohol solution of l-menthol, and the alcohol was evaporated to obtain fine aluminum oxide powder surface-treated with l-menthol. .
【0046】母体トナー粒子95重量部に対し、表面処
理された酸化アルミニウム 5重量部をミキサーにて混
合し、本発明の現像剤(トナー)を得た。A developer (toner) of the present invention was obtained by mixing 5 parts by weight of surface-treated aluminum oxide with 95 parts by weight of the base toner particles in a mixer.
【0047】比較例2
又、比較のためl−メントールにより処理していないメ
カノックスUB−10による現像剤(トナー)も作成し
た。Comparative Example 2 For comparison, a developer (toner) made of Mechanox UB-10 which was not treated with l-menthol was also prepared.
【0048】上記実施例2並びに比較例2によって得た
トナーを用いて実施例1と同様のテストを行った。結果
を表2に示す。なお1000枚コピー後の画像は実施例
2、比較例2共に差はなかった。The same test as in Example 1 was conducted using the toners obtained in Example 2 and Comparative Example 2 above. The results are shown in Table 2. Note that there was no difference in the images after copying 1000 sheets between Example 2 and Comparative Example 2.
【0049】[0049]
【表2】[Table 2]
【0050】実施例3並びに比較例3
実施例1と同様にして母体トナー粒子並びに表面処理さ
れた酸化チタン微粉末を得た。この母体トナー粒子20
0gと安息香酸ベンジルにより表面処理された酸化チタ
ン微粉末1.0gを直径50cm、内部に回転羽根を設
置した密閉容器に入れ、回転羽根の回転数を5000r
pm、容器温度を45℃に保ち、5分間運転し本発明の
現像剤(トナー)を得た。このトナーを用いて現像剤を
作成(キャリア:100μフェライトキャリア)し、複
写機(リコー社製FT−4820)にて1000枚の連
続コピーを行った。補給トナーは300g複写機内にセ
ットした。このとき20人のモニターによる官能テスト
を行った。又、比較のため安息香酸ベンジルにより処理
していないP−25による現像剤(トナー)も作成(比
較例3)して同様のテストを行った。Example 3 and Comparative Example 3 Base toner particles and surface-treated fine titanium oxide powder were obtained in the same manner as in Example 1. This base toner particle 20
0g and 1.0g of titanium oxide fine powder surface-treated with benzyl benzoate were placed in a sealed container with a diameter of 50cm and a rotating blade installed inside, and the rotation speed of the rotating blade was set to 5000 r.
pm, the container temperature was maintained at 45° C., and the operation was continued for 5 minutes to obtain the developer (toner) of the present invention. A developer was prepared using this toner (carrier: 100μ ferrite carrier), and 1000 sheets were continuously copied using a copying machine (FT-4820 manufactured by Ricoh). 300 g of replenishment toner was set in the copying machine. At this time, a sensory test was conducted by 20 monitors. For comparison, a developer (toner) made of P-25 which was not treated with benzyl benzoate was also prepared (Comparative Example 3) and the same test was conducted.
【0051】[0051]
【表3】[Table 3]
【0052】実施例4並びに比較例4
実施例2と同様にして母体トナー粒子並びに表面処理さ
れた酸化アルミニウム微粉末を得た。この母体トナー粒
子200gとl−メントールにより表面処理された酸化
アルミニウム微粉末2.0gを実施例3と同様の方法で
固着処理を行った。ただし、回転羽根の回転数は400
0rpm 、容器の温度は35℃とし、本発明の現像剤
(トナー)を得た。又、比較のため、l−メントールに
より処理していないメカノックスUB−10による現像
剤(トナー)も作成した(比較例4)。これら2種類の
現像剤(トナー)を実施例3と同様のテストを行った。Example 4 and Comparative Example 4 In the same manner as in Example 2, base toner particles and surface-treated aluminum oxide fine powder were obtained. 200 g of the base toner particles and 2.0 g of fine aluminum oxide powder whose surface had been treated with l-menthol were fixed in the same manner as in Example 3. However, the rotation speed of the rotating blade is 400
The developer (toner) of the present invention was obtained at 0 rpm and at a container temperature of 35°C. For comparison, a developer (toner) made of Mechanox UB-10 which was not treated with l-menthol was also prepared (Comparative Example 4). These two types of developers (toners) were tested in the same manner as in Example 3.
【0053】[0053]
【表4】[Table 4]
【0054】実施例5並びに比較例5
実施例1と同様にして母体トナー粒子を得た。この母体
トナー粒子95.0重量部に対し、ジェット粉砕機にて
1.0μに粉砕した活性炭微粉末5.0重量部をミキサ
ーにて混合し本発明の現像剤(トナー)を得た。このト
ナーを用いて現像剤を作成(キャリア: 100μフェ
ライトキャリア)し、複写機(リコー社製FT−482
0)にて1000枚の連続コピーを行った。このとき2
0人のモニターによる官能テストを行った。又、比較の
ため活性炭微粉末の添加していない現像剤(比較例5)
も作成して同様のテストを行った。Example 5 and Comparative Example 5 Base toner particles were obtained in the same manner as in Example 1. A developer (toner) of the present invention was obtained by mixing 95.0 parts by weight of the base toner particles with 5.0 parts by weight of activated carbon fine powder pulverized to 1.0 μm using a jet pulverizer using a mixer. A developer was prepared using this toner (carrier: 100μ ferrite carrier), and a copying machine (FT-482 manufactured by Ricoh Co., Ltd.) was used.
0), 1000 sheets were continuously copied. At this time 2
A sensory test was conducted with 0 monitors. Also, for comparison, a developer without the addition of activated carbon fine powder (Comparative Example 5)
I also created one and conducted a similar test.
【0055】[0055]
【表5】[Table 5]
【0056】実施例6並びに比較例6
トナー処方
スチレン・2−エチルヘキシルアクリレート・
n−ブチルメタ
クリレート共重合体 86.0重量部 低分子
量ポリプロピレン
3.0重量部 ニ
グロシン系染料
1.0重
量部 カーボンブラック
10.0重量部 以上の処方でエクストルーダーを用
いて混練を行い、体積平均粒径10μの母体トナー粒子
を得た。この母体トナー粒子97.0重量部に対し、ジ
ェット粉砕機にて0.7μに粉砕した活性炭微粉末3.
0重量部をミキサーにて混合し、本発明の現像剤(トナ
ー)を得た。このトナーを用いて実施例5と同様100
0枚の連続コピーを行い、20人のモニターによる臭気
の官能テストを行った。又、比較のため活性炭微粉末の
添加していない現像剤(トナー)(比較例6)も作成し
て同様のテストを行った。Example 6 and Comparative Example 6 Toner formulation Styrene/2-ethylhexyl acrylate/
n-Butyl methacrylate copolymer 86.0 parts by weight Low molecular weight polypropylene
3.0 parts by weight Nigrosine dye
1.0 parts by weight carbon black
10.0 parts by weight The above formulation was kneaded using an extruder to obtain base toner particles having a volume average particle diameter of 10 μm. To 97.0 parts by weight of the base toner particles, 3.
0 parts by weight were mixed in a mixer to obtain a developer (toner) of the present invention. Using this toner, 100
A series of 0 copies were made, and an odor sensory test was conducted by 20 monitors. For comparison, a developer (toner) (Comparative Example 6) to which no activated carbon fine powder was added was also prepared and the same test was conducted.
【0057】[0057]
【表6】[Table 6]
【0058】実施例7並びに比較例7
実施例1と同様にして母体トナー粒子を得た。この母体
トナー粒子 200gとジェット粉砕機にて1.0μに
粉砕した活性炭微粉末 5gを直径50cm、内部に回
転羽根を設置した密閉容器に入れ、回転羽根の回転数を
5000rpm、容器温度を45℃に保ち、 5分間運
転し本発明の現像剤(トナー)を得た。このトナーを用
いて現像剤を作成(キャリア:100μフェライトキャ
リア)し、複写機(リコー社製FT−4820)にて1
000枚の連続コピーを行った。このとき20人のモニ
ターによる官能テストを行った。又、比較のため活性炭
微粉末の添加していない現像剤(トナ−)(比較例7)
も作成し、同様のテストを行った。Example 7 and Comparative Example 7 Base toner particles were obtained in the same manner as in Example 1. 200g of the base toner particles and 5g of activated carbon fine powder crushed to 1.0μ with a jet pulverizer were placed in a sealed container with a diameter of 50cm and a rotating blade installed inside, the rotation speed of the rotating blade was set at 5000 rpm, and the temperature of the container was set at 45°C. The developer (toner) of the present invention was obtained by maintaining the temperature at A developer was prepared using this toner (carrier: 100μ ferrite carrier), and a copying machine (FT-4820 manufactured by Ricoh) was used to create a developer.
000 copies were made continuously. At this time, a sensory test was conducted by 20 monitors. Also, for comparison, a developer (toner) without the addition of activated carbon fine powder (Comparative Example 7)
I also created one and conducted a similar test.
【0059】[0059]
【表7】[Table 7]
【0060】実施例8並びに比較例8
実施例7と同様にして母体トナー粒子を得た。この母体
トナー粒子 200gとジェット粉砕機にて0.7μに
粉砕した活性炭微粉末2gを実施例7と同様の方法で固
着処理を行った。ただし、回転羽根の回転数は4000
rpm、容器の温度は40℃とし、本発明の現像剤(ト
ナー)を得た。
このトナーを用いて実施例7と同様1000枚の連続コ
ピーを行い、20人のモニターによる臭気の官能テスト
を行った。又、比較のため活性炭微粉末の添加していな
い現像剤(トナー)(比較例8)も作成して同様のテス
トを行った。Example 8 and Comparative Example 8 Base toner particles were obtained in the same manner as in Example 7. 200 g of the base toner particles and 2 g of activated carbon fine powder ground to 0.7 μm using a jet grinder were subjected to a fixation treatment in the same manner as in Example 7. However, the rotation speed of the rotating blade is 4000
The developer (toner) of the present invention was obtained at rpm and container temperature of 40°C. Using this toner, 1000 copies were made continuously in the same manner as in Example 7, and a sensory odor test was conducted by 20 monitors. For comparison, a developer (toner) (Comparative Example 8) to which no activated carbon fine powder was added was also prepared and the same test was conducted.
【0061】[0061]
【表8】[Table 8]
【0062】実施例9並びに比較例9
実施例1と同様にして母体トナー粒子を得た。この母体
トナー粒子96重量部に対し、SiO2・Al2O3・
ZnO・Li2O・Ag+微粉末(一次粒子平均粒径1
.0μ以下)4重量部をミキサーにて混合し、本発明の
現像剤トナーを得た。このトナーを用いて現像剤を作成
(キャリア:100μフェライトキャリア)し、複写機
(リコー社製FT−4820)にて1000枚の連続コ
ピーを行った。補給用トナーは300g複写機内にセッ
トした。このとき20人のモニターによる官能テストを
行った。又、比較のため、SiO2・Al2O3・Zn
O・Li2O・Ag+微粉末の添加していないトナー(
比較例9)すなわち母体トナー粒子も同様のテストを行
ったExample 9 and Comparative Example 9 Base toner particles were obtained in the same manner as in Example 1. For 96 parts by weight of the base toner particles, SiO2, Al2O3,
ZnO・Li2O・Ag+fine powder (primary particle average particle size 1
.. 0μ or less) were mixed in a mixer to obtain a developer toner of the present invention. A developer was prepared using this toner (carrier: 100μ ferrite carrier), and 1000 sheets were continuously copied using a copying machine (FT-4820 manufactured by Ricoh). 300 g of replenishment toner was set in the copying machine. At this time, a sensory test was conducted by 20 monitors. Also, for comparison, SiO2・Al2O3・Zn
O・Li2O・Ag+Toner without the addition of fine powder (
Comparative Example 9) In other words, the base toner particles were also subjected to the same test.
【0063】[0063]
【表9】[Table 9]
【0064】1000枚コピー後の画像は実施例9、比
較例9ともに差はなかった。There was no difference in the images after copying 1000 sheets between Example 9 and Comparative Example 9.
【0065】実施例10並びに比較例10実施例2と同
様にして母体トナー粒子を得た。この母体トナー粒子9
9重量部に対し、SiO2・Al2O3・ZnO・Li
2O・Ag+微粉末(一次粒子平均粒径1.0μ以下)
1重量部をミキサーにて混合し、本発明の現像剤(トナ
ー)を得た。又、比較のため、SiO2・Al2O3・
ZnO・Li2O・Ag+微粉末の添加していないトナ
ー(比較例10)すなわち母体トナー粒子もテストを行
う。これら2種類のトナーを用い、実施例10と同様の
テストを行った。Example 10 and Comparative Example 10 Base toner particles were obtained in the same manner as in Example 2. This base toner particle 9
For 9 parts by weight, SiO2・Al2O3・ZnO・Li
2O・Ag+fine powder (primary particle average particle size 1.0μ or less)
1 part by weight was mixed in a mixer to obtain a developer (toner) of the present invention. Also, for comparison, SiO2・Al2O3・
A toner without the addition of ZnO.Li2O.Ag+fine powder (Comparative Example 10), ie, base toner particles, is also tested. A test similar to that in Example 10 was conducted using these two types of toner.
【0066】[0066]
【表10】[Table 10]
【0067】1000枚コピー後の画像は実施例10、
比較例10ともに差はなかった。[0067] The images after copying 1000 sheets are Example 10,
There was no difference in Comparative Example 10.
【0068】実施例11並びに比較例11実施例1と同
様にして母体トナー粒子を得た。この母体トナー粒子
200gと、SiO2・Al2O3・ZnO・Li2O
・Ag+微粒子4gを直径50cm、内部に回転羽根を
設置した密閉容器に入れ、回転羽根の回転数を5000
rpm、容器温度を45℃に保ち、5分間運転し、本発
明の現像剤(トナー)を得た。このトナーを用いて現像
剤を作成(キャリア:100μフェライトキャリア)し
、複写機(リコー社製FT−4820)にて1000枚
の連続コピーを行った。補給用トナーは300g複写機
内にセットした。このとき20人のモニターによる官能
テストを行った。又、比較のため、SiO2・Al2O
3・ZnO・Li2O・Ag+微粉末の添加していない
トナー(比較例11)すなわち母体トナー粒子も同様の
テストを行った。Example 11 and Comparative Example 11 Base toner particles were obtained in the same manner as in Example 1. This base toner particle
200g and SiO2, Al2O3, ZnO, Li2O
・Pour 4 g of Ag + fine particles into a sealed container with a diameter of 50 cm and a rotating blade installed inside, and rotate the rotating blade at 5000 rotations.
The rpm and container temperature were maintained at 45° C., and the operation was continued for 5 minutes to obtain a developer (toner) of the present invention. A developer was prepared using this toner (carrier: 100μ ferrite carrier), and 1000 sheets were continuously copied using a copying machine (FT-4820 manufactured by Ricoh). 300 g of replenishment toner was set in the copying machine. At this time, a sensory test was conducted by 20 monitors. Also, for comparison, SiO2・Al2O
3.ZnO.Li2O.Ag+Toner to which no fine powder was added (Comparative Example 11), ie, base toner particles, was also subjected to the same test.
【0069】[0069]
【表11】[Table 11]
【0070】1000枚コピー後の画像は実施例11、
比較例11ともに差はなかった。[0070] The images after copying 1000 sheets are Example 11,
There was no difference in Comparative Example 11.
【0071】実施例12並びに比較例12実施例2と同
様にして母体トナー粒子を得た。この母体トナー粒子2
00gと、SiO2・Al2O3・ZnO・Li2O・
Ag+微粒子2gを実施例11と同様の方法で固着処理
を行った。ただし、回転羽根の回転数は 4000rp
m、容器の温度は35℃とし、本発明の現像剤(トナー
)を得た。又、比較のため、SiO2・Al2O3・Z
nO・Li2O・Ag+微粉末の添加していないトナー
(比較例12)すなわち母体トナー粒子もテストを行う
。これら2種類のトナーを用い、実施例11と同様のテ
ストを行った。Example 12 and Comparative Example 12 Base toner particles were obtained in the same manner as in Example 2. This base toner particle 2
00g and SiO2・Al2O3・ZnO・Li2O・
2 g of Ag+fine particles were fixed in the same manner as in Example 11. However, the rotation speed of the rotating blade is 4000 rpm.
m, the temperature of the container was 35° C., and a developer (toner) of the present invention was obtained. Also, for comparison, SiO2・Al2O3・Z
A toner without the addition of nO.Li2O.Ag+fine powder (Comparative Example 12), ie, base toner particles, is also tested. A test similar to that in Example 11 was conducted using these two types of toner.
【0072】[0072]
【表12】[Table 12]
【0073】1000枚コピー後の画像は実施例12、
比較例12ともに差はなかった。[0073] The images after copying 1000 sheets are Example 12,
There was no difference in Comparative Example 12.
【0074】実施例13並びに比較例13実施例1と同
様にして母体トナー粒子を得た。この母体トナー粒子
200gと、ジェット粉砕機にて1.0μに粉砕したゼ
オライト微粉末5gを直径50cm、内部に回転羽根を
設置した密閉容器に入れ、回転羽根の回転数を5000
rpm 、容器温度を45℃に保ち、 5分間運転し、
本発明の現像剤(トナー)を得た。このトナーを用いて
現像剤を作成(キャリア:100μフェライトキャリア
)し、複写機(リコー社製FT−4820)にて100
0枚の連続コピーを行った。このとき20人のモニター
による官能テストを行った。又、比較のため、ゼオライ
ト微粉末の添加していないトナー(比較例13)も作成
し、同様のテストを行った。Example 13 and Comparative Example 13 Base toner particles were obtained in the same manner as in Example 1. This base toner particle
200g and 5g of zeolite fine powder crushed to 1.0μ with a jet crusher were placed in a sealed container with a diameter of 50cm and a rotating blade installed inside, and the rotation speed of the rotating blade was set to 5000.
rpm, keep the container temperature at 45°C, run for 5 minutes,
A developer (toner) of the present invention was obtained. A developer was prepared using this toner (carrier: 100μ ferrite carrier), and a 100μ
Continuous copying of 0 sheets was performed. At this time, a sensory test was conducted by 20 monitors. For comparison, a toner (Comparative Example 13) to which no zeolite fine powder was added was also prepared, and the same test was conducted.
【0075】[0075]
【表13】[Table 13]
【0076】実施例14並びに比較例14実施例6と同
様にして母体トナー粒子を得た。この母体トナー粒子
200gとジェット粉砕機にて 0.7μに粉砕したゼ
オライト微粉末 2gを実施例1と同様の方法で固着処
理を行った。ただし、回転羽根の回転数は4000rp
m、容器の温度は40℃とし、本発明の現像剤(トナー
)を得た。このトナーを用いて実施例13と同様100
0枚の連続コピーを行い、20人のモニターによる臭気
の官能テストを行った。又、比較のためゼオライト微粉
末の添加していない現像剤(トナー)(比較例14)も
作成して同様のテストを行った。Example 14 and Comparative Example 14 Base toner particles were obtained in the same manner as in Example 6. This base toner particle
A fixation treatment was performed in the same manner as in Example 1 using 200 g and 2 g of zeolite fine powder crushed to 0.7 μm using a jet crusher. However, the rotation speed of the rotating blade is 4000 rpm.
m, the temperature of the container was 40° C., and a developer (toner) of the present invention was obtained. Using this toner, 100
A series of 0 copies were made, and an odor sensory test was conducted by 20 monitors. For comparison, a developer (toner) (Comparative Example 14) to which no zeolite fine powder was added was also prepared and the same test was conducted.
【0077】[0077]
【表14】[Table 14]
【0078】実施例15並びに比較例15実施例1と同
様にして母体トナー粒子を得た。この母体トナー粒子9
5.0重量部に対し、ジェット粉砕機にて1.0μに粉
砕したゼオライト微粉末 5.0重量部をミキサーにて
混合し、本発明の現像剤(トナー)を得た。このトナー
を用いて現像剤を作成(キャリア:100μフェライト
キャリア)し、複写機(リコー社製FT−4820)に
て1000枚の連続コピーを行った。このとき20人の
モニターによる官能テストを行った。又、比較のためゼ
オライト微粉末の添加していないトナー(比較例15)
も作成して同様のテストを行ったExample 15 and Comparative Example 15 Base toner particles were obtained in the same manner as in Example 1. This base toner particle 9
A developer (toner) of the present invention was obtained by mixing 5.0 parts by weight of zeolite fine powder pulverized to 1.0 μm with a jet pulverizer in a mixer. A developer was prepared using this toner (carrier: 100μ ferrite carrier), and 1000 sheets were continuously copied using a copying machine (FT-4820 manufactured by Ricoh). At this time, a sensory test was conducted by 20 monitors. Also, for comparison, a toner without the addition of zeolite fine powder (Comparative Example 15)
I also created and ran a similar test.
【0079】[0079]
【表15】[Table 15]
【0080】実施例16並びに比較例16実施例2と同
様にして母体トナー粒子を得た。この母体トナー粒子9
7.0重量部に対し、ジェット粉砕機にて0.7μに粉
砕したゼオライト微粉末 3.0重量部をミキサーにて
混合し、本発明のトナーを得た。このトナーを用いて実
施例1と同様1000枚の連続コピーを行い、20人の
モニターによる臭気の官能テストを行った。又、比較の
ためゼオライト微粉末の添加していない現像剤(トナー
)(比較例16)も作成して同様のテストを行った。Example 16 and Comparative Example 16 Base toner particles were obtained in the same manner as in Example 2. This base toner particle 9
To 7.0 parts by weight, 3.0 parts by weight of fine zeolite powder ground to 0.7 μm using a jet pulverizer was mixed in a mixer to obtain the toner of the present invention. Using this toner, 1000 sheets were continuously copied in the same manner as in Example 1, and an odor sensory test was conducted by 20 monitors. For comparison, a developer (toner) (Comparative Example 16) to which no zeolite fine powder was added was also prepared and the same test was conducted.
【0081】[0081]
【表16】[Table 16]
【0082】[0082]
【発明の効果】本発明の現像剤は複写機内や定着時にお
いて特有の好ましい香気を放ちあるいは不快臭を吸着、
分解するので、不快臭を感ずることがなく、事務室内の
執務環境が良くなり、しかも複写画像が悪影響を受ける
ことがない。Effects of the Invention The developer of the present invention emits a unique pleasant aroma or absorbs unpleasant odors in the copying machine or during fixing.
Since it decomposes, there is no unpleasant odor, the working environment in the office is improved, and the copied images are not adversely affected.
Claims (4)
トナー粒子と、香料によりその表面を処理された微粉末
とを含有したことを特徴とする電子写真乾式現像剤。1. An electrophotographic dry developer comprising toner particles whose main components are a binder resin and a colorant, and a fine powder whose surface is treated with a fragrance.
求項1記載の電子写真乾式現像剤。2. The electrophotographic dry developer according to claim 1, wherein fine powder is adhered to toner particles.
トナー粒子と、活性炭、無機質ゲルおよびゼオライトか
ら選択された微粉末とを含有したことを特徴とする電子
写真乾式現像剤。3. An electrophotographic dry developer comprising toner particles containing a binder resin and a colorant as main components, and a fine powder selected from activated carbon, inorganic gel, and zeolite.
びゼオライトから選択された微粒子が固着してなる請求
項3記載の電子写真乾式現像剤。4. The electrophotographic dry developer according to claim 3, wherein fine particles selected from activated carbon, inorganic gel, and zeolite are fixed to the toner particles.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP3143314A JPH04338970A (en) | 1990-06-29 | 1991-06-14 | Electrophotographic dry developer |
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP17132490 | 1990-06-29 | ||
JP2-171324 | 1990-06-29 | ||
JP3143314A JPH04338970A (en) | 1990-06-29 | 1991-06-14 | Electrophotographic dry developer |
Publications (1)
Publication Number | Publication Date |
---|---|
JPH04338970A true JPH04338970A (en) | 1992-11-26 |
Family
ID=26475076
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP3143314A Pending JPH04338970A (en) | 1990-06-29 | 1991-06-14 | Electrophotographic dry developer |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH04338970A (en) |
Cited By (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US6057072A (en) * | 1997-03-31 | 2000-05-02 | Eastman Kodak Company | Toner compositions containing activated carbons |
EP1482382A1 (en) * | 2003-04-04 | 2004-12-01 | Kao Corporation | Toner for electrostatic image development |
US7252916B2 (en) | 2003-09-01 | 2007-08-07 | Samsung Electronics Co., Ltd. | Electro-photographic developing agent |
CN103149811A (en) * | 2012-11-09 | 2013-06-12 | 广州市科密办公科技有限公司 | Aroma type powdered ink and preparation method thereof |
JP2015075742A (en) * | 2013-10-11 | 2015-04-20 | 京セラドキュメントソリューションズ株式会社 | Toner for electrophotographic device |
-
1991
- 1991-06-14 JP JP3143314A patent/JPH04338970A/en active Pending
Cited By (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US6057072A (en) * | 1997-03-31 | 2000-05-02 | Eastman Kodak Company | Toner compositions containing activated carbons |
EP1482382A1 (en) * | 2003-04-04 | 2004-12-01 | Kao Corporation | Toner for electrostatic image development |
US7252916B2 (en) | 2003-09-01 | 2007-08-07 | Samsung Electronics Co., Ltd. | Electro-photographic developing agent |
CN103149811A (en) * | 2012-11-09 | 2013-06-12 | 广州市科密办公科技有限公司 | Aroma type powdered ink and preparation method thereof |
JP2015075742A (en) * | 2013-10-11 | 2015-04-20 | 京セラドキュメントソリューションズ株式会社 | Toner for electrophotographic device |
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