JPH026966A - Developer for electrostatic latent image - Google Patents
Developer for electrostatic latent imageInfo
- Publication number
- JPH026966A JPH026966A JP63156846A JP15684688A JPH026966A JP H026966 A JPH026966 A JP H026966A JP 63156846 A JP63156846 A JP 63156846A JP 15684688 A JP15684688 A JP 15684688A JP H026966 A JPH026966 A JP H026966A
- Authority
- JP
- Japan
- Prior art keywords
- latent image
- electrostatic latent
- developer
- compd
- resins
- 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
- 239000003086 colorant Substances 0.000 claims abstract description 27
- 239000007787 solid Substances 0.000 claims abstract description 10
- 150000002894 organic compounds Chemical class 0.000 claims description 12
- 239000000463 material Substances 0.000 abstract description 11
- 239000000203 mixture Substances 0.000 abstract description 5
- 239000001993 wax Substances 0.000 abstract description 5
- 230000015572 biosynthetic process Effects 0.000 abstract description 3
- 239000003989 dielectric material Substances 0.000 abstract description 3
- 238000000034 method Methods 0.000 description 26
- 239000000758 substrate Substances 0.000 description 15
- 229920005989 resin Polymers 0.000 description 12
- 239000011347 resin Substances 0.000 description 12
- 239000002245 particle Substances 0.000 description 9
- -1 silver halide Chemical class 0.000 description 9
- 229910052751 metal Inorganic materials 0.000 description 7
- 239000002184 metal Substances 0.000 description 7
- 150000003839 salts Chemical class 0.000 description 7
- 239000000975 dye Substances 0.000 description 6
- 239000000049 pigment Substances 0.000 description 5
- XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 description 4
- 239000007788 liquid Substances 0.000 description 4
- 229920003227 poly(N-vinyl carbazole) Polymers 0.000 description 4
- RSWGJHLUYNHPMX-UHFFFAOYSA-N Abietic-Saeure Natural products C12CCC(C(C)C)=CC2=CCC2C1(C)CCCC2(C)C(O)=O RSWGJHLUYNHPMX-UHFFFAOYSA-N 0.000 description 3
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 3
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
- 229920000180 alkyd Polymers 0.000 description 3
- 239000003795 chemical substances by application Substances 0.000 description 3
- 229920001577 copolymer Polymers 0.000 description 3
- 239000003623 enhancer Substances 0.000 description 3
- 238000010438 heat treatment Methods 0.000 description 3
- 238000002844 melting Methods 0.000 description 3
- 230000008018 melting Effects 0.000 description 3
- PYWVYCXTNDRMGF-UHFFFAOYSA-N rhodamine B Chemical compound [Cl-].C=12C=CC(=[N+](CC)CC)C=C2OC2=CC(N(CC)CC)=CC=C2C=1C1=CC=CC=C1C(O)=O PYWVYCXTNDRMGF-UHFFFAOYSA-N 0.000 description 3
- XDOFQFKRPWOURC-UHFFFAOYSA-N 16-methylheptadecanoic acid Chemical compound CC(C)CCCCCCCCCCCCCCC(O)=O XDOFQFKRPWOURC-UHFFFAOYSA-N 0.000 description 2
- 239000004925 Acrylic resin Substances 0.000 description 2
- 229920000178 Acrylic resin Polymers 0.000 description 2
- 229910002012 Aerosil® Inorganic materials 0.000 description 2
- 229910000967 As alloy Inorganic materials 0.000 description 2
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 2
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 2
- KHPCPRHQVVSZAH-HUOMCSJISA-N Rosin Natural products O(C/C=C/c1ccccc1)[C@H]1[C@H](O)[C@@H](O)[C@@H](O)[C@@H](CO)O1 KHPCPRHQVVSZAH-HUOMCSJISA-N 0.000 description 2
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 2
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 2
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 2
- 239000011324 bead Substances 0.000 description 2
- 229910052799 carbon Inorganic materials 0.000 description 2
- 230000007423 decrease Effects 0.000 description 2
- 239000006185 dispersion Substances 0.000 description 2
- POULHZVOKOAJMA-UHFFFAOYSA-N dodecanoic acid Chemical compound CCCCCCCCCCCC(O)=O POULHZVOKOAJMA-UHFFFAOYSA-N 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 229920001971 elastomer Polymers 0.000 description 2
- 239000010419 fine particle Substances 0.000 description 2
- YBMRDBCBODYGJE-UHFFFAOYSA-N germanium dioxide Chemical compound O=[Ge]=O YBMRDBCBODYGJE-UHFFFAOYSA-N 0.000 description 2
- 239000011521 glass Substances 0.000 description 2
- 239000000944 linseed oil Substances 0.000 description 2
- 235000021388 linseed oil Nutrition 0.000 description 2
- LQERIDTXQFOHKA-UHFFFAOYSA-N nonadecane Chemical compound CCCCCCCCCCCCCCCCCCC LQERIDTXQFOHKA-UHFFFAOYSA-N 0.000 description 2
- 239000012860 organic pigment Substances 0.000 description 2
- 239000003973 paint Substances 0.000 description 2
- 239000012188 paraffin wax Substances 0.000 description 2
- 235000019271 petrolatum Nutrition 0.000 description 2
- 229920001568 phenolic resin Polymers 0.000 description 2
- 239000005011 phenolic resin Substances 0.000 description 2
- 229920000642 polymer Polymers 0.000 description 2
- 150000003097 polyterpenes Chemical class 0.000 description 2
- 239000005060 rubber Substances 0.000 description 2
- 239000004065 semiconductor Substances 0.000 description 2
- KHPCPRHQVVSZAH-UHFFFAOYSA-N trans-cinnamyl beta-D-glucopyranoside Natural products OC1C(O)C(O)C(CO)OC1OCC=CC1=CC=CC=C1 KHPCPRHQVVSZAH-UHFFFAOYSA-N 0.000 description 2
- 239000002699 waste material Substances 0.000 description 2
- 239000011787 zinc oxide Substances 0.000 description 2
- QGKMIGUHVLGJBR-UHFFFAOYSA-M (4z)-1-(3-methylbutyl)-4-[[1-(3-methylbutyl)quinolin-1-ium-4-yl]methylidene]quinoline;iodide Chemical compound [I-].C12=CC=CC=C2N(CCC(C)C)C=CC1=CC1=CC=[N+](CCC(C)C)C2=CC=CC=C12 QGKMIGUHVLGJBR-UHFFFAOYSA-M 0.000 description 1
- WRIDQFICGBMAFQ-UHFFFAOYSA-N (E)-8-Octadecenoic acid Natural products CCCCCCCCCC=CCCCCCCC(O)=O WRIDQFICGBMAFQ-UHFFFAOYSA-N 0.000 description 1
- BFRLRGJQKQUFHK-UHFFFAOYSA-N 2,2-bis(hydroxymethyl)propane-1,3-diol;phthalic acid Chemical compound OCC(CO)(CO)CO.OC(=O)C1=CC=CC=C1C(O)=O BFRLRGJQKQUFHK-UHFFFAOYSA-N 0.000 description 1
- CNPVJWYWYZMPDS-UHFFFAOYSA-N 2-methyldecane Chemical compound CCCCCCCCC(C)C CNPVJWYWYZMPDS-UHFFFAOYSA-N 0.000 description 1
- LQJBNNIYVWPHFW-UHFFFAOYSA-N 20:1omega9c fatty acid Natural products CCCCCCCCCCC=CCCCCCCCC(O)=O LQJBNNIYVWPHFW-UHFFFAOYSA-N 0.000 description 1
- HNNQYHFROJDYHQ-UHFFFAOYSA-N 3-(4-ethylcyclohexyl)propanoic acid 3-(3-ethylcyclopentyl)propanoic acid Chemical compound CCC1CCC(CCC(O)=O)C1.CCC1CCC(CCC(O)=O)CC1 HNNQYHFROJDYHQ-UHFFFAOYSA-N 0.000 description 1
- BTXXTMOWISPQSJ-UHFFFAOYSA-N 4,4,4-trifluorobutan-2-one Chemical compound CC(=O)CC(F)(F)F BTXXTMOWISPQSJ-UHFFFAOYSA-N 0.000 description 1
- NKFIBMOQAPEKNZ-UHFFFAOYSA-N 5-amino-1h-indole-2-carboxylic acid Chemical compound NC1=CC=C2NC(C(O)=O)=CC2=C1 NKFIBMOQAPEKNZ-UHFFFAOYSA-N 0.000 description 1
- QSBYPNXLFMSGKH-UHFFFAOYSA-N 9-Heptadecensaeure Natural products CCCCCCCC=CCCCCCCCC(O)=O QSBYPNXLFMSGKH-UHFFFAOYSA-N 0.000 description 1
- BQACOLQNOUYJCE-FYZZASKESA-N Abietic acid Natural products CC(C)C1=CC2=CC[C@]3(C)[C@](C)(CCC[C@@]3(C)C(=O)O)[C@H]2CC1 BQACOLQNOUYJCE-FYZZASKESA-N 0.000 description 1
- 229910002016 Aerosil® 200 Inorganic materials 0.000 description 1
- LSNNMFCWUKXFEE-UHFFFAOYSA-M Bisulfite Chemical compound OS([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-M 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- 241000254173 Coleoptera Species 0.000 description 1
- 229920000742 Cotton Polymers 0.000 description 1
- 244000043261 Hevea brasiliensis Species 0.000 description 1
- 239000005639 Lauric acid Substances 0.000 description 1
- 239000005642 Oleic acid Substances 0.000 description 1
- ZQPPMHVWECSIRJ-UHFFFAOYSA-N Oleic acid Natural products CCCCCCCCC=CCCCCCCCC(O)=O ZQPPMHVWECSIRJ-UHFFFAOYSA-N 0.000 description 1
- 239000004264 Petrolatum Substances 0.000 description 1
- 240000004713 Pisum sativum Species 0.000 description 1
- 235000010582 Pisum sativum Nutrition 0.000 description 1
- 239000005062 Polybutadiene Substances 0.000 description 1
- 239000004698 Polyethylene Substances 0.000 description 1
- 239000004743 Polypropylene Substances 0.000 description 1
- 229920000297 Rayon Polymers 0.000 description 1
- BUGBHKTXTAQXES-UHFFFAOYSA-N Selenium Chemical compound [Se] BUGBHKTXTAQXES-UHFFFAOYSA-N 0.000 description 1
- 235000021355 Stearic acid Nutrition 0.000 description 1
- ULUAUXLGCMPNKK-UHFFFAOYSA-N Sulfobutanedioic acid Chemical class OC(=O)CC(C(O)=O)S(O)(=O)=O ULUAUXLGCMPNKK-UHFFFAOYSA-N 0.000 description 1
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical class CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 1
- 239000005083 Zinc sulfide Substances 0.000 description 1
- QLNFINLXAKOTJB-UHFFFAOYSA-N [As].[Se] Chemical compound [As].[Se] QLNFINLXAKOTJB-UHFFFAOYSA-N 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 125000000217 alkyl group Chemical group 0.000 description 1
- 229910000147 aluminium phosphate Inorganic materials 0.000 description 1
- 239000012164 animal wax 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
- ZCGHEBMEQXMRQL-UHFFFAOYSA-N benzyl 2-carbamoylpyrrolidine-1-carboxylate Chemical compound NC(=O)C1CCCN1C(=O)OCC1=CC=CC=C1 ZCGHEBMEQXMRQL-UHFFFAOYSA-N 0.000 description 1
- LKVJLQKCWWNRJC-UHFFFAOYSA-N buta-1,3-diene prop-2-enylbenzene Chemical compound C=CC=C.C(C1=CC=CC=C1)C=C LKVJLQKCWWNRJC-UHFFFAOYSA-N 0.000 description 1
- VLLYOYVKQDKAHN-UHFFFAOYSA-N buta-1,3-diene;2-methylbuta-1,3-diene Chemical compound C=CC=C.CC(=C)C=C VLLYOYVKQDKAHN-UHFFFAOYSA-N 0.000 description 1
- QHIWVLPBUQWDMQ-UHFFFAOYSA-N butyl prop-2-enoate;methyl 2-methylprop-2-enoate;prop-2-enoic acid Chemical compound OC(=O)C=C.COC(=O)C(C)=C.CCCCOC(=O)C=C QHIWVLPBUQWDMQ-UHFFFAOYSA-N 0.000 description 1
- 239000001030 cadmium pigment Substances 0.000 description 1
- 125000004432 carbon atom Chemical group C* 0.000 description 1
- 239000004203 carnauba wax Substances 0.000 description 1
- 235000013869 carnauba wax Nutrition 0.000 description 1
- IRPXADUBAQAOKL-UHFFFAOYSA-N chembl1408927 Chemical compound C1=CC=C2C(N=NC3=C4C=CC(=CC4=CC(=C3O)S(O)(=O)=O)S(O)(=O)=O)=CC=C(S(O)(=O)=O)C2=C1 IRPXADUBAQAOKL-UHFFFAOYSA-N 0.000 description 1
- 239000001031 chromium pigment Substances 0.000 description 1
- 239000011248 coating agent Substances 0.000 description 1
- 238000000576 coating method Methods 0.000 description 1
- 239000001032 cobalt pigment Substances 0.000 description 1
- XCJYREBRNVKWGJ-UHFFFAOYSA-N copper(II) phthalocyanine Chemical compound [Cu+2].C12=CC=CC=C2C(N=C2[N-]C(C3=CC=CC=C32)=N2)=NC1=NC([C]1C=CC=CC1=1)=NC=1N=C1[C]3C=CC=CC3=C2[N-]1 XCJYREBRNVKWGJ-UHFFFAOYSA-N 0.000 description 1
- 230000000593 degrading effect Effects 0.000 description 1
- 238000010586 diagram Methods 0.000 description 1
- 235000014113 dietary fatty acids Nutrition 0.000 description 1
- NJDNXYGOVLYJHP-UHFFFAOYSA-L disodium;2-(3-oxido-6-oxoxanthen-9-yl)benzoate Chemical compound [Na+].[Na+].[O-]C(=O)C1=CC=CC=C1C1=C2C=CC(=O)C=C2OC2=CC([O-])=CC=C21 NJDNXYGOVLYJHP-UHFFFAOYSA-L 0.000 description 1
- 125000003438 dodecyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 238000003379 elimination reaction Methods 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 230000005496 eutectics Effects 0.000 description 1
- 239000000194 fatty acid Substances 0.000 description 1
- 229930195729 fatty acid Natural products 0.000 description 1
- 150000004665 fatty acids Chemical class 0.000 description 1
- 235000010985 glycerol esters of wood rosin Nutrition 0.000 description 1
- 150000008282 halocarbons Chemical class 0.000 description 1
- 239000001023 inorganic pigment Substances 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- QXJSBBXBKPUZAA-UHFFFAOYSA-N isooleic acid Natural products CCCCCCCC=CCCCCCCCCC(O)=O QXJSBBXBKPUZAA-UHFFFAOYSA-N 0.000 description 1
- PBOSTUDLECTMNL-UHFFFAOYSA-N lauryl acrylate Chemical compound CCCCCCCCCCCCOC(=O)C=C PBOSTUDLECTMNL-UHFFFAOYSA-N 0.000 description 1
- 238000012423 maintenance Methods 0.000 description 1
- 229910044991 metal oxide Inorganic materials 0.000 description 1
- 150000004706 metal oxides Chemical class 0.000 description 1
- 125000005395 methacrylic acid group Chemical group 0.000 description 1
- 239000004200 microcrystalline wax Substances 0.000 description 1
- 235000019808 microcrystalline wax Nutrition 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 239000000178 monomer Substances 0.000 description 1
- 229920003052 natural elastomer Polymers 0.000 description 1
- 239000000025 natural resin Substances 0.000 description 1
- 229920001194 natural rubber Polymers 0.000 description 1
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 1
- OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-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
- 229940065472 octyl acrylate Drugs 0.000 description 1
- ANISOHQJBAQUQP-UHFFFAOYSA-N octyl prop-2-enoate Chemical compound CCCCCCCCOC(=O)C=C ANISOHQJBAQUQP-UHFFFAOYSA-N 0.000 description 1
- 239000003921 oil Substances 0.000 description 1
- 235000019198 oils Nutrition 0.000 description 1
- ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid Chemical compound CCCCCCCC\C=C/CCCCCCCC(O)=O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 description 1
- TWNQGVIAIRXVLR-UHFFFAOYSA-N oxo(oxoalumanyloxy)alumane Chemical compound O=[Al]O[Al]=O TWNQGVIAIRXVLR-UHFFFAOYSA-N 0.000 description 1
- 235000019809 paraffin wax Nutrition 0.000 description 1
- 229940066842 petrolatum Drugs 0.000 description 1
- 239000012169 petroleum derived wax Substances 0.000 description 1
- 235000019381 petroleum wax Nutrition 0.000 description 1
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N phenol group Chemical group C1(=CC=CC=C1)O ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 1
- 239000012165 plant wax Substances 0.000 description 1
- 229920006122 polyamide resin Polymers 0.000 description 1
- 229920002857 polybutadiene Polymers 0.000 description 1
- 229920005668 polycarbonate resin Polymers 0.000 description 1
- 239000004431 polycarbonate resin Substances 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
- 229920000098 polyolefin Polymers 0.000 description 1
- 229920001155 polypropylene Polymers 0.000 description 1
- 229920002689 polyvinyl acetate Polymers 0.000 description 1
- 239000011118 polyvinyl acetate Substances 0.000 description 1
- 239000004800 polyvinyl chloride Substances 0.000 description 1
- 229920000915 polyvinyl chloride Polymers 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 238000001556 precipitation Methods 0.000 description 1
- HJWLCRVIBGQPNF-UHFFFAOYSA-N prop-2-enylbenzene Chemical compound C=CCC1=CC=CC=C1 HJWLCRVIBGQPNF-UHFFFAOYSA-N 0.000 description 1
- 229930195734 saturated hydrocarbon Natural products 0.000 description 1
- 229910052711 selenium Inorganic materials 0.000 description 1
- 239000011669 selenium Substances 0.000 description 1
- 230000001235 sensitizing effect Effects 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 229910052709 silver Inorganic materials 0.000 description 1
- 239000004332 silver Substances 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 241000894007 species Species 0.000 description 1
- 230000003068 static effect Effects 0.000 description 1
- 239000008117 stearic acid Substances 0.000 description 1
- 229920003048 styrene butadiene rubber Polymers 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 229920003051 synthetic elastomer Polymers 0.000 description 1
- 229920003002 synthetic resin Polymers 0.000 description 1
- 239000000057 synthetic resin Substances 0.000 description 1
- 239000005061 synthetic rubber Substances 0.000 description 1
- 229910052714 tellurium Inorganic materials 0.000 description 1
- 235000013799 ultramarine blue Nutrition 0.000 description 1
- 235000015112 vegetable and seed oil Nutrition 0.000 description 1
- 239000008158 vegetable oil Substances 0.000 description 1
- 229910052984 zinc sulfide Inorganic materials 0.000 description 1
- DRDVZXDWVBGGMH-UHFFFAOYSA-N zinc;sulfide Chemical compound [S-2].[Zn+2] DRDVZXDWVBGGMH-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- G—PHYSICS
- G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
- G03G—ELECTROGRAPHY; ELECTROPHOTOGRAPHY; MAGNETOGRAPHY
- G03G9/00—Developers
- G03G9/08—Developers with toner particles
- G03G9/12—Developers with toner particles in liquid developer mixtures
- G03G9/13—Developers with toner particles in liquid developer mixtures characterised by polymer components
-
- G—PHYSICS
- G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
- G03G—ELECTROGRAPHY; ELECTROPHOTOGRAPHY; MAGNETOGRAPHY
- G03G9/00—Developers
- G03G9/08—Developers with toner particles
- G03G9/12—Developers with toner particles in liquid developer mixtures
- G03G9/125—Developers with toner particles in liquid developer mixtures characterised by the liquid
Landscapes
- Physics & Mathematics (AREA)
- General Physics & Mathematics (AREA)
- Liquid Developers In Electrophotography (AREA)
Abstract
Description
【発明の詳細な説明】
〔産業上の利用分野〕
本発明は、電子写真プロセス等において静電潜像を湿式
現像する際に使用される静電潜像現像剤に関するもので
ある。DETAILED DESCRIPTION OF THE INVENTION [Industrial Field of Application] The present invention relates to an electrostatic latent image developer used when wet-developing an electrostatic latent image in an electrophotographic process or the like.
〔従来の技術]
画像形成技術の分野において、−様に帯電させた光導電
体上に画像信号に応し”ζ選択的に光照射を(〒い、形
成された静電潜像を現像する方式は一般に静電写真プロ
セスと呼ばれている。この静電写真プロセスには、大別
して乾式現像法と湿現像法とがある。[Prior Art] In the field of image forming technology, a photoconductor charged in a negative manner is selectively irradiated with light in response to an image signal to develop an electrostatic latent image formed. This method is generally called an electrostatic photographic process.The electrostatic photographic process is broadly divided into a dry developing method and a wet developing method.
乾式現像法は、原理的に静電潜像に単に着色剤の粉末を
散布し付着させるだけなので、取り扱い性および現像ト
ナー剤の保存性に優れるという長所を有している。しか
しながら、電子スチル写真を印画するビデオプリンタ等
に見られるごとく、近年高まりつつある高品位画像への
要望に対応するには、湿式現像法に一歩譲らざるを得な
いのが実情である。The dry development method, in principle, simply scatters and adheres coloring agent powder to the electrostatic latent image, so it has the advantage of being excellent in handling and the storage stability of the developed toner. However, in order to meet the increasing demand for high-quality images that has been increasing in recent years, as seen in video printers that print electronic still photographs, the reality is that we have no choice but to give way to wet developing methods.
これに対して湿式現像法は、着色剤としての染料あるい
は顔料を絶縁性媒体中に分散させた液体現像剤を使用す
る方式である。湿式現像法によれば、銀塩写真に匹敵す
る解像度と階調を得ることが可能であるほか、特に着色
剤として顔料を使用した場合には形成された画像の耐候
性に優れており、各方面で開発が進められている。On the other hand, the wet development method uses a liquid developer in which a dye or pigment as a coloring agent is dispersed in an insulating medium. According to the wet development method, it is possible to obtain resolution and gradation comparable to silver halide photography, and the weather resistance of the formed image is excellent, especially when pigments are used as colorants. Development is underway in this area.
この湿式現像法の原理は第1図により説明される。この
図は便宜上、−枚の長い感光基材(1)に対して各工程
が順次通用されてゆくものとして示しである。まr、帯
電工程にて感光基材(1)がコロナ放電体(2)等の適
当な帯電手段を用いてたとえばマイナスに一様に帯電さ
れる。次の露光工程では、半導体赤外レーザー光源(3
)等の適当な露光手段を用いて画像情報に対応した選択
的な光照射が行われ、露光された部位のマイナス電荷が
消失する。次の現像工程では、上述のようにして静電潜
像の形成された感光基材(1)が現像タンク(4)のト
を通過する。」二記現像タンク(4)の中には、液体状
の絶縁性媒体(5)中にプラスに帯電した着色剤粒子(
6)が分散された静電潜像現像剤が入っており、これが
感光基材(1)と接触すると該着色剤粒子(6)がマ・
イナス電荷のある部位に向かって泳動し付着する。最後
の定着工程において、不要部分に付着した着色剤粒子(
6)が除去され、除電工程を経て感光基材(1)上に画
像が形成される。The principle of this wet development method is explained with reference to FIG. For convenience, this figure is shown assuming that each step is sequentially applied to a long photosensitive substrate (1). In the charging step, the photosensitive substrate (1) is uniformly charged, for example, negatively, using a suitable charging means such as a corona discharger (2). In the next exposure process, a semiconductor infrared laser light source (3
) or the like is used to selectively irradiate light corresponding to the image information, and the negative charge on the exposed area disappears. In the next developing step, the photosensitive substrate (1) on which the electrostatic latent image has been formed as described above passes through the developing tank (4). In the developing tank (4), positively charged colorant particles (
6) is dispersed therein, and when this comes into contact with the photosensitive substrate (1), the colorant particles (6) are dispersed in the colorant particles (6).
It migrates toward a negatively charged site and attaches to it. During the final fixing process, colorant particles (
6) is removed, and an image is formed on the photosensitive substrate (1) through a static elimination process.
ところで従来のン!式現像法において静電潜像現像剤に
使用されている絶縁性媒体は、たとえば飽和炭化水素系
のアイソパーG(エッソ社製)に代表される常温で液体
状の物質であった。しかしながら、かかる静電潜像現像
剤には、本来均一に分散されるべき着色剤粒子が凝集・
沈澱を起こし易いという欠点がある。また、現像工程が
繰り返されて着色剤の濃度が低下すると、保存性が低下
するという問題もある。さらに、上記絶縁性媒体は高分
子有機化合物であり、常に安定した画像形成を実現する
ためにこれを頻繁に交換することは、メンテナンスが煩
雑であるばかりか、廃液処理の観点からも好ましいこと
ではない。By the way, the conventional n! The insulating medium used in the electrostatic latent image developer in the formula development method is a substance that is liquid at room temperature, such as saturated hydrocarbon-based Isopar G (manufactured by Esso). However, in such electrostatic latent image developers, colorant particles that should originally be uniformly dispersed aggregate and
It has the disadvantage of being prone to precipitation. Furthermore, if the concentration of the colorant decreases due to repeated development steps, there is also the problem that storage stability decreases. Furthermore, the above-mentioned insulating medium is a high-molecular organic compound, and replacing it frequently in order to always achieve stable image formation is not only complicated in maintenance, but also undesirable from the perspective of waste liquid treatment. do not have.
そこで本発明は、上述のような不都合を生ずることなく
、取り扱い性に優れ、常に安定した画像形成を可能とす
る静電潜像現像剤の堤供を目的とする。SUMMARY OF THE INVENTION Therefore, the present invention aims to provide an electrostatic latent image developer which does not cause the above-mentioned inconveniences, is easy to handle, and enables stable image formation at all times.
〔課題を解決するための手段]
本発明者らは、上述の目的を達成するために鋭意検討を
行った結果、従来の液体状の電気絶縁性媒体に代わり、
常温で固体であり、平均分子量2000以下の電気絶縁
性有機化合物に着色剤を分散させることが有効であるこ
とを見出し、本発明に至ったものである。[Means for Solving the Problems] As a result of intensive studies to achieve the above-mentioned object, the present inventors have developed a method that replaces the conventional liquid electrically insulating medium.
The inventors have discovered that it is effective to disperse a colorant in an electrically insulating organic compound that is solid at room temperature and has an average molecular weight of 2000 or less, leading to the present invention.
すなわち本発明にかかる静電潜像現像剤は、常温で固体
であり、平均分子12000以下の電気絶縁性有機化合
物に着色剤が分散されてなることを特徴とするものであ
る。That is, the electrostatic latent image developer according to the present invention is solid at room temperature and is characterized by being made of an electrically insulating organic compound having an average molecular weight of 12,000 or less and a colorant dispersed therein.
本発明において使用される電気絶縁性有機化合物は、少
なくとも常温で固体である平均分子量2000未満の有
機化合物である。平均分子種の下限は特に規定されるも
のではないが、実用的には通常の使用環境において揮発
しなければ良いのでおよそ200である。融点は通常の
使用環境や取り扱い性を考慮して30°C以上とし、よ
り好ましくは40°C以上である。融点の上限は特に規
定されるものではないが、実用的にはおよそ100 ’
C1より好ましくは80°C以下である。これは、あま
り高過ぎても加熱に余分なエネルギーを消費すること、
上記絶縁性有機化合物を使用して調製される静電潜像現
像剤をたとえばシート状の基材の上に形成して使用する
場合に、基材として一般に使用される材料の耐熱温度を
越えてはならないこと等を考慮するからである。The electrically insulating organic compound used in the present invention is an organic compound that is solid at least at room temperature and has an average molecular weight of less than 2,000. The lower limit of the average molecular species is not particularly defined, but practically it is approximately 200 as long as it does not volatilize in the normal usage environment. The melting point is set to be 30°C or higher, more preferably 40°C or higher, taking into consideration the normal use environment and ease of handling. The upper limit of the melting point is not particularly defined, but practically it is around 100'
The temperature is more preferably 80°C or less than C1. This means that even if the temperature is too high, extra energy will be consumed for heating.
When an electrostatic latent image developer prepared using the above-mentioned insulating organic compound is used, for example, by forming it on a sheet-like base material, the temperature exceeds the heat-resistant temperature of the material generally used as the base material. This is because consideration must be given to things that should not be done.
これらの要求を満たす材料としては、パラフィン類、ロ
ウ類、およびこれらの混合物が挙げられる。まずパラフ
ィン類としては、ノナデカンからヘキサコンクンに至る
炭素数19〜60の各種の正パラフィンがある。またロ
ウ類としては、カルナウバロウ1綿ロウ等の植物ロウ、
ミツ1コウ等の動物ロウ、オシケライト、およびパラフ
ィンロウ、微晶ロウ、ペトロラタム等の石油ロウ等が挙
げられる。これらの材料は、誘電率εが1.9〜2.3
程度の誘電体である。Materials that meet these requirements include paraffins, waxes, and mixtures thereof. First, as paraffins, there are various normal paraffins having 19 to 60 carbon atoms, ranging from nonadecane to hexaconcune. In addition, waxes include plant waxes such as carnauba wax 1 cotton wax,
Examples include animal waxes such as beetle wax, osichelite, and petroleum waxes such as paraffin wax, microcrystalline wax, and petrolatum. These materials have a dielectric constant ε of 1.9 to 2.3.
It is a dielectric material of about
上記電気絶縁性有機化合物に分散される着色剤としては
、従来公知の無機顔料、有Ja顔料、染料およびこれら
の混合物が使用できる。As the coloring agent dispersed in the electrically insulating organic compound, conventionally known inorganic pigments, Ja-containing pigments, dyes, and mixtures thereof can be used.
たとえば無ms料としては、クロム系顔料、カドミウム
系顔料、鉄系顔料、コバルト系顔料、群青、紺青等が挙
げられる。また、有機顔料や染料としでは、ハンザイエ
ロー(C,1,11680)、ヘンジジンイエローG
(C,1,21090)、ヘンジジンオレンジ(C,1
,21110)、ファーストレッド(C91,3708
5)、ブリリアントカーミツ3 B (C,f、16
015−Lake)、フタロシアニンブルー(C,1,
74160) 、ビクトリアブルー(C,1,4259
5−1、ake) 、スピリットブラック(C,1,5
0415) 、オイルブルー(C,1,74350)、
アルカリブルー(C,1,42770^)、ファースト
スカーレット (C,1,12315)、ローダミン6
B (C,1,45160)、ローダミンレーキ (
C,1,45160−Lake) 、ファーストスカイ
ブルー(C,1,74200−Lake) 、ニグロシ
ン(C,1,50415) 、カーボンブラ7り等が挙
げられる。For example, non-ms pigments include chromium pigments, cadmium pigments, iron pigments, cobalt pigments, ultramarine blue, navy blue, and the like. In addition, as organic pigments and dyes, Hansa Yellow (C, 1, 11680), Henjijin Yellow G
(C, 1, 21090), Hengejin Orange (C, 1
, 21110), Fast Red (C91, 3708)
5), Brilliant Karmitsu 3 B (C, f, 16
015-Lake), Phthalocyanine Blue (C, 1,
74160), Victoria Blue (C, 1,4259
5-1, ake), Spirit Black (C, 1, 5
0415), Oil Blue (C, 1,74350),
Alkaline Blue (C, 1,42770^), First Scarlet (C, 1, 12315), Rhodamine 6
B (C,1,45160), rhodamine lake (
C, 1,45160-Lake), Fast Sky Blue (C, 1,74200-Lake), Nigrosine (C, 1,50415), Carbon Blur 7, and the like.
これらは単独でも2種以上の混合物としても用いること
ができる。These can be used alone or as a mixture of two or more.
本発明にかかる静電潜像現像には、上述の電気絶縁性有
機化合物と着色剤のほか、分散性や着色剤の定着性を向
上させる目的で樹脂を併用しても良い。かかる樹脂とし
ては公知の材料を適宜選択して使用することができ、例
示すればブタジェンゴム スチレン−ブタジェンゴム2
環化ゴム、天然ゴム等のゴム類、スチレン系樹脂、ビニ
ルトルエン系樹脂、アクリル系樹脂、メタクリル系樹脂
。In the electrostatic latent image development according to the present invention, in addition to the above-mentioned electrically insulating organic compound and colorant, a resin may be used in combination for the purpose of improving the dispersibility and fixing properties of the colorant. As such resin, known materials can be selected and used as appropriate, examples include butadiene rubber, styrene-butadiene rubber 2
Rubbers such as cyclized rubber and natural rubber, styrene resins, vinyltoluene resins, acrylic resins, and methacrylic resins.
ポリエステル系樹脂、ポリカーボネート系樹脂5ポリ酢
酸ビニル系樹脂等の合成樹脂類、ロジン系樹脂、水素添
加ロジン系樹脂、アマニ油変成アルキド樹脂等の変成ア
ルキドを含むアルキド樹脂類、ポリテルペン類等の天然
樹脂類等が挙げられる。Synthetic resins such as polyester resins, polycarbonate resins, polyvinyl acetate resins, alkyd resins including modified alkyds such as rosin resins, hydrogenated rosin resins, linseed oil modified alkyd resins, and natural resins such as polyterpenes. etc.
その他、フェノール樹脂類、フェノールホルマリン樹脂
等の変成フェノール樹脂類、フタル酸ペンタエリトリッ
ト、クマロン−インデン樹脂類、エステルガム樹脂類、
植物油ポリアミド樹脂類等もを用であるし、ポリ塩化ビ
ニル、塩素化ポリプロピレン等のようなハロゲン化炭化
水素重合体類、ビニルトルエン−ブタジェン、ブタジェ
ン−イソプレン等の合成ゴム#11i、2−エチルへキ
シルメタクリレ−1・、ラウリルメククリレ−1・、ス
テアリルメククリレート、ラウリルアクリレート、オク
チルアクリレート等の長鎖アルキル基を持つアクリル糸
上ツマ−の重合体類もしくはそれらと他の重合性モノマ
ーとの共重合体類(たとえば、スチレン−ラウリルメタ
クリレート共重合体、アクリル酸−ラウリルメタクリレ
ート共重合体等)、ポリエチレン等のポリオレフィン類
、ポリテルペン類等も使用できる。In addition, phenolic resins, modified phenolic resins such as phenol-formalin resin, pentaerythritol phthalate, coumaron-indene resins, ester gum resins,
Vegetable oil polyamide resins etc. can also be used, halogenated hydrocarbon polymers such as polyvinyl chloride, chlorinated polypropylene etc., synthetic rubbers such as vinyltoluene-butadiene, butadiene-isoprene etc. #11i, 2-ethyl Polymers of acrylic yarns having long-chain alkyl groups such as xyl methacrylate-1, lauryl methacrylate-1, stearyl methacrylate, lauryl acrylate, and octyl acrylate, or these and other polymerizable monomers Copolymers with (for example, styrene-lauryl methacrylate copolymer, acrylic acid-lauryl methacrylate copolymer, etc.), polyolefins such as polyethylene, polyterpenes, etc. can also be used.
さらに、上記静電潜像現像剤には通常は電荷供与剤が添
加され、本発明もその例外ではない。使用される電荷供
与剤は、たとえばナフテン酸、オクテン酸、オレイン酸
、ステアリン酸、イソステアリン酸あるいはラウリン酸
等の脂肪酸の金属塩、スルホコハク酸エステル類の金属
塩、油溶性スルホン酸金属塩、リン酸エステル金属塩、
アビエチン酸等の金属塩、芳香族カルボン酸金属塩、芳
香族スルホン酸金属塩等である。Further, a charge donor is usually added to the electrostatic latent image developer, and the present invention is no exception to this. The charge-donating agents used are, for example, metal salts of fatty acids such as naphthenic acid, octenoic acid, oleic acid, stearic acid, isostearic acid or lauric acid, metal salts of sulfosuccinic acid esters, oil-soluble sulfonic acid metal salts, and phosphoric acid. ester metal salt,
These include metal salts such as abietic acid, metal salts of aromatic carboxylic acids, metal salts of aromatic sulfonic acids, and the like.
また、着色剤のIF電電荷を向上させるために、S i
oz、AlzO:+、Ti0z、ZnO,GazOz。Additionally, in order to improve the IF charge of the colorant, Si
oz, AlzO:+, TiOz, ZnO, GazOz.
I nzoz、GeO2,5nOz、Pbog、MgO
等の金属酸化物微粒子やこれらの混合物を電荷増強剤と
して添加しても良い。Inzoz, GeO2, 5nOz, Pbog, MgO
Fine particles of metal oxides such as these or mixtures thereof may be added as a charge enhancer.
上述の各成分の配合比であるが、まず着色剤は電気絶縁
性有機化合物の溶融状態11に対して通常0.01〜1
00 g、好ましくは0.1〜logである。Regarding the blending ratio of each component mentioned above, first, the coloring agent is usually 0.01 to 1 to 11 in the melted state of the electrically insulating organic compound.
00 g, preferably 0.1 to log.
また電荷供与剤は同しく1j2に対して通常0.001
〜log、好ましくは0.01〜Igの範囲である。さ
らに電荷増強剤は、着色剤に対して重量比で2倍以下、
好ましくは同量以下の範囲で添加される。Also, the charge donor is usually 0.001 for 1j2.
-log, preferably 0.01-Ig. Furthermore, the charge enhancer is not more than twice the weight ratio of the colorant,
Preferably, it is added in the same amount or less.
このような静電潜像現像剤は、適当な容器に入れて直接
使用するか、あるいは適当な支持体に塗布あるいは含浸
させる等の方法で使用することができる。使用の際には
静電潜像現像剤が溶融状態に保たれるよう、前述の第1
図に示した現像タンク(4)あるいは上記支持体に対し
て適当な加熱手段を設けることが必要である。Such an electrostatic latent image developer can be used directly by placing it in a suitable container, or by coating or impregnating a suitable support. In order to keep the electrostatic latent image developer in a molten state during use,
It is necessary to provide suitable heating means for the developing tank (4) shown in the figure or for the support described above.
本発明にかかる静電潜像現像剤が適用される静電潜像の
現像プロセスは、通常行われているものであればいかな
るものでも良く、静電潜像の形成方法や感光基材の種類
を問わない。たとえば感光基材に関して言えば、周知の
有機光導電体もしくは無機光導電体からなる感光基材に
対して用いることができる。適用される有機光導電体と
しては、周知の広範囲の有機光導電体が挙げられ、実用
化されでいるものとしてはポリ−N−ビニルカルバゾー
ルと24.7−hリニトロフルオレン−9オンとからな
る′電子写真感光基材、ポリ−Nビニルカルバゾールを
ビリリウム塩基色素で増感したもの、ポリ−N−ビニル
カルバゾールをシアニン系色素で増感したもの、有機顔
料を主成分とする電子写真感光基材、染料と樹脂とから
なる共晶錯体を主体とする電子写真感光基材等が例示さ
れる。無機光!7ilt体としては、酸化亜鉛、硫化亜
鉛、硫化力[ミウム、セレン、セレン−テルル台上、セ
レン−砒素合金、セレン−テルル−砒素合金、非晶質ケ
イソ系)A料等が挙げられる。The electrostatic latent image developing process to which the electrostatic latent image developer according to the present invention is applied may be any commonly used process, including the method of forming the electrostatic latent image and the type of photosensitive substrate. No questions asked. For example, with respect to photosensitive substrates, it can be used for photosensitive substrates made of well-known organic or inorganic photoconductors. The applicable organic photoconductors include a wide range of well-known organic photoconductors, and those that have been put into practical use include poly-N-vinylcarbazole and 24.7-h linitrofluoren-9one. Electrophotographic photosensitive substrates, poly-N-vinylcarbazole sensitized with biryllium base dyes, poly-N-vinylcarbazole sensitized with cyanine-based dyes, electrophotographic photosensitive bases containing organic pigments as main components. Examples include electrophotographic photosensitive substrates mainly composed of eutectic complexes consisting of materials, dyes, and resins. Inorganic light! Examples of the 7ilt material include zinc oxide, zinc sulfide, sulfuric acid (mium, selenium, selenium-tellurium base, selenium-arsenic alloy, selenium-tellurium-arsenic alloy, amorphous siliceous material) A material, and the like.
また、本発明の静電潜像現像剤は感光以夕1の手段、た
とえば帯電↑1−により誘電体の・:1)電等で生じさ
l”だ静電潜像を現像する際にも適用できる。The electrostatic latent image developer of the present invention can also be used when developing an electrostatic latent image generated by photosensitive means, such as charging ↑1-, on a dielectric material. Applicable.
本発明にかかる静電潜像現像剤では、常温で固体である
電気絶縁性有機化合物中に着色剤が均一に分散されてい
る。この静電層像現像剤は使用時には適当な加熱手段に
て溶融状態に保持されており、これに静電潜像の形成さ
れた感光基材が接触すると、その電荷にしたがって選択
的に静電潜像現像剤が付着して画像が形成される。この
静電潜像現像剤は使用時以外は固体であるため、取り扱
い性や保存性に優れている。したがって、メンテナンス
が容易で常に安定した画像形成能を発揮する静電潜像現
像剤の提供が可能となる。In the electrostatic latent image developer according to the present invention, a colorant is uniformly dispersed in an electrically insulating organic compound that is solid at room temperature. This electrostatic layer image developer is kept in a molten state by an appropriate heating means during use, and when it comes into contact with a photosensitive substrate on which an electrostatic latent image has been formed, it selectively generates an electrostatic charge according to its charge. A latent image developer adheres to form an image. Since this electrostatic latent image developer is solid except when in use, it has excellent handling and storage stability. Therefore, it is possible to provide an electrostatic latent image developer that is easy to maintain and always exhibits stable image forming ability.
〔実施例] 以下、本発明の好適な実施例について説明する。〔Example] Hereinafter, preferred embodiments of the present invention will be described.
実施例1
4ζ実施例はシアン色の静電潜像現像剤を調製した例で
ある。Example 1 4ζ Example is an example in which a cyan electrostatic latent image developer was prepared.
まず、着色剤であるリオノール ブルーl<XFl(東
洋インキ社製) 0.625 gおよびイソパラフィン
系溶剤(出光石油社製、商品名I P2825)0.5
gをツーバー・マーシー法により小粒子化し、ペースト
を得た。次に、このペーストを別のイソパラフィン系溶
剤(エノン社製。商品名アイソパーII ) 50 m
p、中に分散し、電荷増強剤としてアルミナ微粒子(
ロ木アエロジル社製、商品名アルミニウムオキサイドC
)0.05gを添加してアルミナビーズと共にペイント
シェーカー中で12時間分散処理を行った。さらに、ア
クリル樹脂(三菱レーヨン社製、商品名FRIOI)の
50%トルエン溶液0.5g、および電荷供与剤となる
ナフテン酸ジルコニウム0.025gとナフテン酸カル
ソウム0.025gを添加し、!a Ifl現像液を得
た。First, 0.625 g of the coloring agent Lionol Blue l
g was made into small particles by the Zuber-Mercy method to obtain a paste. Next, this paste was mixed with 50 m of another isoparaffinic solvent (manufactured by Enon Co., Ltd., trade name: Isopar II).
p, dispersed in alumina fine particles (
Manufactured by Roki Aerosil Co., Ltd., product name Aluminum Oxide C
) 0.05g was added and a dispersion treatment was performed for 12 hours in a paint shaker together with alumina beads. Furthermore, 0.5 g of a 50% toluene solution of acrylic resin (manufactured by Mitsubishi Rayon Co., Ltd., trade name FRIOI), and 0.025 g of zirconium naphthenate and 0.025 g of calcium naphthenate, which serve as charge-donating agents, are added, and! a Ifl developer was obtained.
次に、融点42〜44゛Cのパラフィン120m1を予
め70’Cにて溶融し、上記fA濃縮現像液mj2をご
の中・\分散させて青色の静電潜像現像剤を調製した。Next, 120 ml of paraffin having a melting point of 42 to 44°C was melted in advance at 70°C, and the fA concentrated developer mj2 was dispersed in a bowl to prepare a blue electrostatic latent image developer.
実施例2
本実施例はイエロー色の静電潜像現像剤を調製した例で
ある。Example 2 In this example, a yellow electrostatic latent image developer was prepared.
まず、着色剤であるシミ1ラー・ファスト・イエロー8
GF (大目ドインキ社製)0.5gおよびイソパラフ
ィン系)容剤(出光石油社製、商品名I P2825)
0.5 gをツーバー・マーシー法により小粒子化し
、ペース1−を得た。次に、このペーストを別のイソバ
ラつイン系7容剤(エノソ社製、商品名アイソベー)口
50m2中に分散し、電荷増強剤として超微粒子状無水
シリカ(日本アエロジル社製、商品名アエロジル200
) 0.01 gを添加してガラスビー・ズと共にペイ
ントシェーカー中で18時間分散処理を行った。以下、
濃縮現像液と静電潜像「見像剤の調製方法は実施例1に
記載した方法と同様である。First, the colorant Stain 1 Color Fast Yellow 8
GF (manufactured by Daime Doinki Co., Ltd.) 0.5 g and isoparaffin type) container (manufactured by Idemitsu Oil Co., Ltd., trade name I P2825)
0.5 g was made into small particles by the Zuber-Mercy method to obtain Pace 1-. Next, this paste was dispersed in another 50 m2 of isobaratuine-based 7-container (manufactured by Enoso Co., Ltd., trade name: Isobe), and ultrafine particulate anhydrous silica (manufactured by Nippon Aerosil Co., Ltd., trade name: Aerosil 200) was used as a charge enhancer.
) 0.01 g was added and dispersed in a paint shaker with glass beads for 18 hours. below,
Concentrated developer and electrostatic latent image The method for preparing the viewing agent was the same as that described in Example 1.
実施例3
本実施例はマゼンタ色の静電潜像現像剤を調製した例で
ある。Example 3 In this example, a magenta electrostatic latent image developer was prepared.
まず、着色剤であるシミュラー・ローダミンY1・〜j
−−F(大日本インキ社製)0.8gおよび亜麻仁油0
.5gをツーバー・マーシー法により小粒子化し、ペー
ストを得た。次に、このペーストを別のイソパラフィン
系)容剤(エノン社製。商品名アイソパーI! ) 5
0m !!、中に分散し、ガラスピーズと共にベイン1
ノエーカー中で18時間分散処理を行った。以下、濃縮
現像液と静電潜像現像剤の調製方法は実施例1に記載1
−だ方法と同様である。First, the colorant Simular Rhodamine Y1.~j
--F (manufactured by Dainippon Ink Co., Ltd.) 0.8g and linseed oil 0
.. 5 g was made into small particles by the Zuber-Marsey method to obtain a paste. Next, add this paste to another isoparaffin-based container (manufactured by Enon Co., Ltd., trade name: Isopar I!) 5
0m! ! , dispersed inside, along with glass peas, Bain 1
Dispersion treatment was carried out in Noacre for 18 hours. The method for preparing the concentrated developer and electrostatic latent image developer is described in Example 1 below.
- This is the same as the method.
これら実施例1ないし実施例3において調製された各色
の静電潜像現像剤を使用して、フルカラー画イ象の形成
を試みた。ごこで使用した感光基材は、変成酢酸ビニル
樹脂からなるシー1−(膜厚50μm)の丑に、感光剤
としてポリビニルカルバゾール1t3.増感側として、
/アユ2色累(1]本感光色素社製、商品名N K21
1i92) 0.2m gを含む感光層(1模w−2
00/7 m )が形成されたものである。なお、J−
記感光基材と静電潜像現像剤が接触後直らに固化すると
画像品位を低下させる虞れがあるため、感光基材を固定
するステージを55°Cに加温した。Using the electrostatic latent image developers of each color prepared in Examples 1 to 3, an attempt was made to form a full-color image. The photosensitive substrate used here was C1- (film thickness 50 μm) made of modified vinyl acetate resin, and polyvinyl carbazole 1t3. As the sensitizing side,
/ Ayu 2-color combination (1) Manufactured by Honkokoshiki Co., Ltd., product name N K21
1i92) Photosensitive layer containing 0.2 m g (1 model w-2
00/7 m) was formed. In addition, J-
If the photosensitive substrate and the electrostatic latent image developer solidify immediately after contact, there is a risk of degrading the image quality, so the stage for fixing the photosensitive substrate was heated to 55°C.
ごの結果、解像度、精彩塵に優れた良好な画像が安定し
て得られた。As a result, good images with excellent resolution and sharpness were stably obtained.
(発明の効果〕
以」二の説明からも明らかなように、本発明にかかる静
電潜像現像剤には常温で固体である電気絶縁性有機化合
物が使用されているため、取り扱い性、保存性、および
着色剤その他の添加剤の分散性に優れている。したがっ
て、高品質の画像を安定して得ることができる。また、
使用後には固体状態で廃棄することができるため、廃棄
物処理の観点からも好ましい。(Effects of the Invention) As is clear from the explanation below, since the electrostatic latent image developer according to the present invention uses an electrically insulating organic compound that is solid at room temperature, it is easy to handle and store. It has excellent dispersibility of colorants and other additives.Therefore, it is possible to stably obtain high-quality images.Also,
Since it can be disposed of in a solid state after use, it is also preferable from the viewpoint of waste disposal.
第1図は湿式現像法の原理を説明するための模式図であ
る。
2 ・・
3 ・・・
4 ・・・
5 ・・・
6 ・
感光基材
コrJす放電体
半導体赤外レーザー光源
現像タンク
絶縁性媒体
着色剤粒子
手続十市正書(自発)
平成1年3月31日FIG. 1 is a schematic diagram for explaining the principle of the wet development method. 2 ・・ 3 ・ 4 ・ 5 ・ 6 ・ Photosensitive substrate Correct discharge body Semiconductor Infrared laser light source Developing tank Insulating medium Colorant particles Procedure Toichi official book (self-produced) March 1999 31st of the month
Claims (1)
性有機化合物に着色剤が分散されてなることを特徴とす
る静電潜像現像剤。An electrostatic latent image developer comprising a colorant dispersed in an electrically insulating organic compound that is solid at room temperature and has an average molecular weight of 2,000 or less.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP63156846A JPH026966A (en) | 1988-06-27 | 1988-06-27 | Developer for electrostatic latent image |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP63156846A JPH026966A (en) | 1988-06-27 | 1988-06-27 | Developer for electrostatic latent image |
Publications (1)
Publication Number | Publication Date |
---|---|
JPH026966A true JPH026966A (en) | 1990-01-11 |
Family
ID=15636651
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP63156846A Pending JPH026966A (en) | 1988-06-27 | 1988-06-27 | Developer for electrostatic latent image |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH026966A (en) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5187955A (en) * | 1991-09-20 | 1993-02-23 | G. A. Braun, Inc. | Center shaft dye injection apparatus |
US5783350A (en) * | 1995-12-14 | 1998-07-21 | Fuji Xerox Co., Ltd. | Developer for electrostatic photography and image forming method |
-
1988
- 1988-06-27 JP JP63156846A patent/JPH026966A/en active Pending
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5187955A (en) * | 1991-09-20 | 1993-02-23 | G. A. Braun, Inc. | Center shaft dye injection apparatus |
US5783350A (en) * | 1995-12-14 | 1998-07-21 | Fuji Xerox Co., Ltd. | Developer for electrostatic photography and image forming method |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
US5045425A (en) | Electrophotographic liquid developer composition and novel charge directors for use therein | |
JP3489032B2 (en) | Liquid developer containing charge control agent for electrostatic photography | |
US3772199A (en) | Liquid developer used for electrophotography | |
EP0278502A2 (en) | Inorganic metal salt as adjuvant for negative liquid electrostatic developers | |
US3909433A (en) | Liquid electrophotographic developing compositions | |
US5071727A (en) | Positively chargeable electrostatic toner containing organic metal complex or organic nitrogen, phosphino or metal compound | |
US4780389A (en) | Inorganic metal salt as adjuvant for negative liquid electrostatic developers | |
JP2674104B2 (en) | Electrostatic latent image developing method | |
JPH026966A (en) | Developer for electrostatic latent image | |
JPH0548468B2 (en) | ||
US3971659A (en) | Color electrophotographic process using photoconductive particles in liquid developer | |
JPH08160675A (en) | Wet toner and manufacture thereof | |
JP2764950B2 (en) | Image forming method | |
JP2764940B2 (en) | Image forming method | |
JP3077184B2 (en) | Wet developer for electrostatic latent image development | |
US6335136B1 (en) | Developer compositions and processes | |
US4618558A (en) | Liquid developer for use in electrostatic photography | |
JPH01172845A (en) | Liquid developer for developing electrostatic latent image | |
US4183818A (en) | Color electrophotographic liquid developer of colored particles and zinc oxide | |
JPH02205853A (en) | Image forming material | |
JPS6254276A (en) | Positive chargeability toner | |
JPH03196152A (en) | Wet developer for developing electrostatic latent image | |
JPH01257860A (en) | Liquid developer for developing electrostatic latent image | |
CA2172434C (en) | Electrophotographic toner and developer compositions and color reproduction processes using same | |
JPH063850A (en) | Electrophotographic developer |