JPH026965A - Developing material for developing electrostatic latent image - Google Patents
Developing material for developing electrostatic latent imageInfo
- Publication number
- JPH026965A JPH026965A JP63156849A JP15684988A JPH026965A JP H026965 A JPH026965 A JP H026965A JP 63156849 A JP63156849 A JP 63156849A JP 15684988 A JP15684988 A JP 15684988A JP H026965 A JPH026965 A JP H026965A
- Authority
- JP
- Japan
- Prior art keywords
- developer
- developing
- electrostatic latent
- latent image
- substrate
- 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.)
- Granted
Links
- 239000000463 material Substances 0.000 title claims abstract description 28
- 239000003086 colorant Substances 0.000 claims abstract description 25
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- 239000007788 liquid Substances 0.000 claims abstract description 13
- 239000007787 solid Substances 0.000 claims abstract description 8
- 238000001816 cooling Methods 0.000 claims abstract description 5
- 239000000758 substrate Substances 0.000 claims description 47
- 238000011161 development Methods 0.000 claims description 14
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- WZCQRUWWHSTZEM-UHFFFAOYSA-N 1,3-phenylenediamine Chemical compound NC1=CC=CC(N)=C1 WZCQRUWWHSTZEM-UHFFFAOYSA-N 0.000 description 3
- 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
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 3
- 229920000180 alkyd Polymers 0.000 description 3
- 229910052799 carbon Inorganic materials 0.000 description 3
- 239000003795 chemical substances by application Substances 0.000 description 3
- 239000000975 dye Substances 0.000 description 3
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- XOLBLPGZBRYERU-UHFFFAOYSA-N tin dioxide Chemical compound O=[Sn]=O XOLBLPGZBRYERU-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
- LSNNMFCWUKXFEE-UHFFFAOYSA-M Bisulfite Chemical compound OS([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-M 0.000 description 2
- 229920000742 Cotton Polymers 0.000 description 2
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 2
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- 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
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 2
- 125000000217 alkyl group Chemical group 0.000 description 2
- 239000000919 ceramic Substances 0.000 description 2
- POULHZVOKOAJMA-UHFFFAOYSA-N dodecanoic acid Chemical compound CCCCCCCCCCCC(O)=O POULHZVOKOAJMA-UHFFFAOYSA-N 0.000 description 2
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- LQERIDTXQFOHKA-UHFFFAOYSA-N nonadecane Chemical compound CCCCCCCCCCCCCCCCCCC LQERIDTXQFOHKA-UHFFFAOYSA-N 0.000 description 2
- 239000011368 organic material Substances 0.000 description 2
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- 229920001155 polypropylene Polymers 0.000 description 2
- 150000003097 polyterpenes Chemical class 0.000 description 2
- 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 2
- 239000005060 rubber 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
- 238000012546 transfer Methods 0.000 description 2
- WRIDQFICGBMAFQ-UHFFFAOYSA-N (E)-8-Octadecenoic acid Natural products CCCCCCCCCC=CCCCCCCC(O)=O WRIDQFICGBMAFQ-UHFFFAOYSA-N 0.000 description 1
- OSNILPMOSNGHLC-UHFFFAOYSA-N 1-[4-methoxy-3-(piperidin-1-ylmethyl)phenyl]ethanone Chemical compound COC1=CC=C(C(C)=O)C=C1CN1CCCCC1 OSNILPMOSNGHLC-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
- WDQMWEYDKDCEHT-UHFFFAOYSA-N 2-ethylhexyl 2-methylprop-2-enoate Chemical group CCCCC(CC)COC(=O)C(C)=C WDQMWEYDKDCEHT-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
- 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
- 229920000178 Acrylic resin Polymers 0.000 description 1
- 239000004925 Acrylic resin Substances 0.000 description 1
- 244000025254 Cannabis sativa Species 0.000 description 1
- 235000012766 Cannabis sativa ssp. sativa var. sativa Nutrition 0.000 description 1
- 235000012765 Cannabis sativa ssp. sativa var. spontanea Nutrition 0.000 description 1
- 229920008712 Copo Polymers 0.000 description 1
- 244000043261 Hevea brasiliensis Species 0.000 description 1
- 239000005639 Lauric acid Substances 0.000 description 1
- 241001465754 Metazoa Species 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
- 229930182556 Polyacetal Natural products 0.000 description 1
- 239000005062 Polybutadiene Substances 0.000 description 1
- 229920005830 Polyurethane Foam Polymers 0.000 description 1
- BQCADISMDOOEFD-UHFFFAOYSA-N Silver Chemical compound [Ag] BQCADISMDOOEFD-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
- 239000002253 acid Substances 0.000 description 1
- WLDHEUZGFKACJH-UHFFFAOYSA-K amaranth Chemical compound [Na+].[Na+].[Na+].C12=CC=C(S([O-])(=O)=O)C=C2C=C(S([O-])(=O)=O)C(O)=C1N=NC1=CC=C(S([O-])(=O)=O)C2=CC=CC=C12 WLDHEUZGFKACJH-UHFFFAOYSA-K 0.000 description 1
- 239000012164 animal wax Substances 0.000 description 1
- 125000003118 aryl group Chemical group 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
- 235000013871 bee wax Nutrition 0.000 description 1
- 239000012166 beeswax Substances 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
- 235000009120 camo Nutrition 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
- 235000005607 chanvre indien Nutrition 0.000 description 1
- 239000000460 chlorine Substances 0.000 description 1
- 229910052801 chlorine Inorganic materials 0.000 description 1
- VNNRSPGTAMTISX-UHFFFAOYSA-N chromium nickel Chemical compound [Cr].[Ni] VNNRSPGTAMTISX-UHFFFAOYSA-N 0.000 description 1
- 239000001031 chromium pigment Substances 0.000 description 1
- 239000001032 cobalt pigment Substances 0.000 description 1
- 238000004040 coloring Methods 0.000 description 1
- 239000002131 composite material Substances 0.000 description 1
- 229920001940 conductive polymer Polymers 0.000 description 1
- 230000000593 degrading effect Effects 0.000 description 1
- 238000000151 deposition Methods 0.000 description 1
- 238000010586 diagram Methods 0.000 description 1
- 239000003989 dielectric material Substances 0.000 description 1
- 235000014113 dietary fatty acids Nutrition 0.000 description 1
- GMSCBRSQMRDRCD-UHFFFAOYSA-N dodecyl 2-methylprop-2-enoate Chemical compound CCCCCCCCCCCCOC(=O)C(C)=C GMSCBRSQMRDRCD-UHFFFAOYSA-N 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
- 238000010292 electrical insulation Methods 0.000 description 1
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- 239000004744 fabric Substances 0.000 description 1
- 239000000194 fatty acid Substances 0.000 description 1
- 229930195729 fatty acid Natural products 0.000 description 1
- 150000004665 fatty acids Chemical class 0.000 description 1
- 239000010419 fine particle Substances 0.000 description 1
- 239000006260 foam Substances 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 235000010985 glycerol esters of wood rosin Nutrition 0.000 description 1
- 239000011487 hemp Substances 0.000 description 1
- 229920001519 homopolymer Polymers 0.000 description 1
- 229910010272 inorganic material Inorganic materials 0.000 description 1
- 239000011147 inorganic material Substances 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- 230000001678 irradiating effect Effects 0.000 description 1
- QXJSBBXBKPUZAA-UHFFFAOYSA-N isooleic acid Natural products CCCCCCCC=CCCCCCCCCC(O)=O QXJSBBXBKPUZAA-UHFFFAOYSA-N 0.000 description 1
- 235000021388 linseed oil Nutrition 0.000 description 1
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- 238000012423 maintenance Methods 0.000 description 1
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- 125000005395 methacrylic acid group Chemical group 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
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- 239000012811 non-conductive material Substances 0.000 description 1
- 239000004745 nonwoven fabric Substances 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
- 238000010422 painting Methods 0.000 description 1
- 239000012188 paraffin wax Substances 0.000 description 1
- 235000019809 paraffin wax Nutrition 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- 229940066842 petrolatum Drugs 0.000 description 1
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- 229920001568 phenolic resin Polymers 0.000 description 1
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- 150000003014 phosphoric acid esters Chemical class 0.000 description 1
- 229920002401 polyacrylamide Polymers 0.000 description 1
- 229920000058 polyacrylate Polymers 0.000 description 1
- 229920006122 polyamide resin Polymers 0.000 description 1
- 229920002857 polybutadiene Polymers 0.000 description 1
- 229920000515 polycarbonate Polymers 0.000 description 1
- 239000004417 polycarbonate Substances 0.000 description 1
- 229920005668 polycarbonate resin Polymers 0.000 description 1
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- 229920000728 polyester Polymers 0.000 description 1
- 229920001225 polyester resin Polymers 0.000 description 1
- 239000004645 polyester resin Substances 0.000 description 1
- 229920000139 polyethylene terephthalate Polymers 0.000 description 1
- 239000005020 polyethylene terephthalate Substances 0.000 description 1
- 229920006254 polymer film Polymers 0.000 description 1
- 229920000098 polyolefin Polymers 0.000 description 1
- 229920006324 polyoxymethylene Polymers 0.000 description 1
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- 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
- HJWLCRVIBGQPNF-UHFFFAOYSA-N prop-2-enylbenzene Chemical compound C=CCC1=CC=CC=C1 HJWLCRVIBGQPNF-UHFFFAOYSA-N 0.000 description 1
- 238000011160 research Methods 0.000 description 1
- 230000000717 retained effect Effects 0.000 description 1
- 229910001220 stainless steel Inorganic materials 0.000 description 1
- 239000010935 stainless steel Substances 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
- 229920003051 synthetic elastomer Polymers 0.000 description 1
- 239000012209 synthetic fiber Substances 0.000 description 1
- 229920002994 synthetic fiber 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
- 229910001887 tin oxide Inorganic materials 0.000 description 1
- 235000013799 ultramarine blue Nutrition 0.000 description 1
- 238000007740 vapor deposition Methods 0.000 description 1
- 235000015112 vegetable and seed oil Nutrition 0.000 description 1
- 239000008158 vegetable oil Substances 0.000 description 1
- 239000012178 vegetable wax Substances 0.000 description 1
- 235000013311 vegetables Nutrition 0.000 description 1
- 239000002699 waste material Substances 0.000 description 1
- 210000002268 wool Anatomy 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
- G03G9/097—Plasticisers; Charge controlling agents
- G03G9/09708—Inorganic compounds
-
- G—PHYSICS
- G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
- G03G—ELECTROGRAPHY; ELECTROPHOTOGRAPHY; MAGNETOGRAPHY
- G03G13/00—Electrographic processes using a charge pattern
- G03G13/01—Electrographic processes using a charge pattern for multicoloured copies
- G03G13/013—Electrographic processes using a charge pattern for multicoloured copies characterised by the developing step, e.g. the properties of the colour developers
- G03G13/0131—Electrographic processes using a charge pattern for multicoloured copies characterised by the developing step, e.g. the properties of the colour developers developing using a step for liquid development, e.g. plural liquid color developers
-
- G—PHYSICS
- G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
- G03G—ELECTROGRAPHY; ELECTROPHOTOGRAPHY; MAGNETOGRAPHY
- G03G13/00—Electrographic processes using a charge pattern
- G03G13/06—Developing
-
- G—PHYSICS
- G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
- G03G—ELECTROGRAPHY; ELECTROPHOTOGRAPHY; MAGNETOGRAPHY
- G03G13/00—Electrographic processes using a charge pattern
- G03G13/22—Processes involving a combination of more than one step according to groups G03G13/02 - G03G13/20
-
- G—PHYSICS
- G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
- G03G—ELECTROGRAPHY; ELECTROPHOTOGRAPHY; MAGNETOGRAPHY
- G03G15/00—Apparatus for electrographic processes using a charge pattern
- G03G15/06—Apparatus for electrographic processes using a charge pattern for developing
-
- 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
- G03G9/09—Colouring agents for toner particles
- G03G9/0902—Inorganic compounds
-
- 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
- G03G9/09—Colouring agents for toner particles
- G03G9/0906—Organic dyes
-
- 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
- G03G9/097—Plasticisers; Charge controlling agents
- G03G9/09708—Inorganic compounds
- G03G9/09725—Silicon-oxides; Silicates
-
- 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
-
- G—PHYSICS
- G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
- G03G—ELECTROGRAPHY; ELECTROPHOTOGRAPHY; MAGNETOGRAPHY
- G03G13/00—Electrographic processes using a charge pattern
- G03G13/01—Electrographic processes using a charge pattern for multicoloured copies
- G03G13/013—Electrographic processes using a charge pattern for multicoloured copies characterised by the developing step, e.g. the properties of the colour developers
- G03G13/0133—Electrographic processes using a charge pattern for multicoloured copies characterised by the developing step, e.g. the properties of the colour developers developing using a step for deposition of subtractive colorant developing compositions, e.g. cyan, magenta and yellow
Landscapes
- Physics & Mathematics (AREA)
- General Physics & Mathematics (AREA)
- Chemical & Material Sciences (AREA)
- Inorganic Chemistry (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より形成された静電潜
像を湿式現像する静電潜像現像用現像材に関するもので
あり、特に21式現像剤でありながらテープ、シート等
として取り汲える新規な静電潜像現像用現像材に関する
ものである。DETAILED DESCRIPTION OF THE INVENTION [Field of Industrial Application] The present invention relates to a developer for developing an electrostatic latent image by wet developing an electrostatic latent image formed by an electrophotographic process, etc. The present invention relates to a novel developer for developing electrostatic latent images that can be used as a tape, sheet, etc. although it is a developer.
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じて選択的に光照射を行い、形成さ
れた静電潜像を現像する方式は、−71に静電写真プロ
セスと呼ばれている。In the field of image forming technology, a method of selectively irradiating light on a photoconductor charged in the negative direction according to an image signal and developing the formed electrostatic latent image is known as -71 electrostatic photography. called a process.
かかる静電写真プロセスにおいて、特に静電潜像を現像
する手法としては、乾式現像法と湿式現像法とが知られ
ており、“それぞれ長所、短所を有することから用途等
に応じて使い分けているのが現状である。In such an electrostatic photographic process, dry development methods and wet development methods are known as methods for developing electrostatic latent images, and "each has advantages and disadvantages, so they are used depending on the purpose etc." is the current situation.
例えば、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、取り扱い性及び
トナーの保存性に優れるという長所を有する反面、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。For example, the dry development method, in principle, simply scatters and adheres colorant powder to the electrostatic latent image, so it has the advantage of being easy to handle and has excellent toner storage stability. The reality is that in order to meet the increasing demand for high-quality images in recent years, as seen in printers, etc., we have no choice but to give way to wet developing methods.
一方、湿式現像法は、着色剤としての染料あるいは顔料
を絶縁性液杖媒体中に分散させた液体現像剤を使用する
方式であって、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が耐候性に優れたものとなる
等の利点を有するものの、現像剤が液体であることから
、例えば常に安定した画像形成を実現するためには頻繁
なメンテナンスが必要になる等、取り扱い性の点で非常
に不利である。On the other hand, the wet development method uses a liquid developer in which dyes or pigments as colorants are dispersed in an insulating liquid medium, and it is possible to obtain resolution and gradation comparable to silver halide photography. In addition, the use of pigments as colorants has the advantage that the formed image has excellent weather resistance, but since the developer is a liquid, it is not possible to produce images that are always stable, for example. In order to realize this formation, frequent maintenance is required, which is very disadvantageous in terms of ease of handling.
ところで、乾式現像法、湿式現像法のいずれにしろ、使
用する現像装置は一般に装置構成が複雑で大掛かりなも
のとなる傾向にあり、例えば一般家庭用等の民生用の画
像形成装置に採用するのは難しい。Incidentally, regardless of whether the dry developing method or the wet developing method is used, the developing devices used generally tend to have complicated and large-scale device configurations, and are not suitable for use in, for example, consumer image forming devices such as those for home use. is difficult.
このような状況から、例えば前述のビデオプリンタ等で
は、装置構成を簡略化を図るために、昇華性インクをザ
ーマルヘソドによって気化させて記録紙に転写する昇華
型熱転写方式やインクジェット方式等によるものが多い
。Under these circumstances, in order to simplify the device configuration, for example, in the video printers mentioned above, many use a sublimation thermal transfer method or inkjet method, in which sublimation ink is vaporized by a thermal head and transferred to recording paper. .
しかしながら、これらの方式は当然のことながら解像度
1階調性等の点で前述の静電写真プロセスには及ばず、
ましてや銀塩写真に匹敵する画像の形成はほとんど不可
能である。However, these methods naturally fall short of the electrostatic photographic process mentioned above in terms of resolution, single gradation, etc.
Furthermore, it is almost impossible to form an image comparable to silver halide photography.
そこで本発明は、かかる従来の実情に鑑みて提案された
ものであって、湿式現像による高画像品位と県華型熱転
写方式等と同等の取り扱い性の良さを併せ持つ新規な静
電潜像現像用現像材を提供するごとを目的とする。Therefore, the present invention has been proposed in view of the conventional situation, and is a novel method for developing electrostatic latent images that has both the high image quality achieved by wet development and the ease of handling equivalent to that of the Kenka type thermal transfer method. The purpose is to provide developing materials.
さらに本発明は、バイアス電圧の印加により画像の4度
1階調性1色バランス等をコントロールすることが可能
な静電潜像現像用現像+4を提供することを目的とする
。A further object of the present invention is to provide a developer +4 for developing an electrostatic latent image, which is capable of controlling the 4 degrees, 1 gradation, 1 color balance, etc. of an image by applying a bias voltage.
本発明者等は、上述の目的を達成するために鋭意研究を
重ねた結果、従来の液体状の電気絶縁性媒体に代わり、
常温で固体であり加熱冷却によって固液変化する有機物
を使用することで、ン易式現像剤をシート化、テープ化
することができ、その取り扱い性を大幅に改善すること
ができること、さらにシート化、テープ化する際に基体
に導電性を持たせることで現像に際して容易にバイアス
電圧を印加することができること、等を知見するに至っ
た。As a result of extensive research in order to achieve the above-mentioned objective, the present inventors have discovered that, in place of the conventional liquid electrically insulating medium,
By using organic substances that are solid at room temperature and change into solid-liquid when heated and cooled, easy-to-use developers can be made into sheets or tapes, which greatly improves their handling. They have discovered that by making the substrate conductive when it is made into a tape, it is possible to easily apply a bias voltage during development.
本発明は、かかる知見に基づいて完成されたものであっ
て、少なくとも常温で固体であり加熱冷却により固液変
化する電気絶縁性有機物に着色剤が分散されてなる現像
剤が導電性を有する基体に保持されていることを特徴と
するものである。The present invention has been completed based on such knowledge, and a developer comprising a coloring agent dispersed in an electrically insulating organic material that is solid at least at room temperature and changes into a solid-liquid upon heating and cooling is a conductive substrate. It is characterized by being held in
ここで、導電性を有する基体とは、基体自体が導電性を
有する材料で形成されたものであってもよいし、非導電
性材料よりなるベース材に導電層を形成したものであっ
てもよい。Here, the conductive substrate may be one in which the substrate itself is made of a conductive material, or one in which a conductive layer is formed on a base material made of a non-conductive material. good.
また、基体に保持される現像剤は、単色であってもよい
し、例えばイエロー、マゼンタ、シアン。Further, the developer held on the substrate may be of a single color, such as yellow, magenta, or cyan.
さらには必要に応じてブランク等、互いに異なる色の着
色剤が分散されたものであってもよい。Furthermore, if necessary, a blank or the like in which colorants of mutually different colors are dispersed may be used.
後者の場合、各色の現像剤を所定の領域で塗り分けるよ
うにすればよく、これら各領域の現像剤で順次静電潜像
を現像するようにすれば、フルカラー画像の形成が可能
である。In the latter case, a full-color image can be formed by applying developer of each color separately in predetermined areas, and by sequentially developing an electrostatic latent image with the developer in each area.
さらに、複数色の現像剤領域を形成した場合、特に加熱
により液状となったときの各現像剤間の混色を防止する
ために、各現像剤領域間に何らかの混色防止層を設けて
もよい。Furthermore, when developer regions of multiple colors are formed, some kind of color mixture prevention layer may be provided between each developer region in order to prevent color mixing between the developer materials, especially when the developer becomes liquid due to heating.
本発明の静電潜像現像用現像材において、基体に保持さ
れた現像剤は、加熱冷却によって固液変化し、加熱状態
で静電潜像に接触せしめることで湿式現像剤として機能
する。In the developer for developing electrostatic latent images of the present invention, the developer held on the substrate changes into a solid-liquid by heating and cooling, and functions as a wet developer by bringing it into contact with the electrostatic latent image in a heated state.
また、前記現像剤は、基体に保持されているので、昇華
型インクフィルム等と同様シート状、テープ状等で取り
扱われ、その取り扱い性や保存性が格段に向上する。Furthermore, since the developer is held on the substrate, it can be handled in the form of a sheet, tape, etc., similar to a sublimation ink film, and its handling and storage stability are greatly improved.
さらに、基体が導電性を有することから、現像に際して
バイアス電圧が容易に印加され、着色剤の付着の度合が
制御されて濃度1階調性1色バランス等が調整される。Further, since the substrate is conductive, a bias voltage can be easily applied during development, the degree of adhesion of the colorant is controlled, and the density, single gradation, single color balance, etc. can be adjusted.
以下、本発明を適用した具体的な実施例について図面を
参照しながら説明する。Hereinafter, specific embodiments to which the present invention is applied will be described with reference to the drawings.
先ず、実施例の説明に先立って、各実施例で使用される
現像剤について説明する。First, prior to explaining the examples, the developer used in each example will be explained.
本発明で使用される現像剤は、少なくとも常温で固体で
あり加熱冷却により固液変化する電気絶縁性有機物に着
色剤が分散されてなるものである。The developer used in the present invention is made by dispersing a colorant in an electrically insulating organic substance that is solid at least at room temperature and changes into a solid-liquid state when heated and cooled.
ここで、電気絶縁性有機物は、少なくとも常温で固体で
ある有機物である。融点は通常の使用環境や取り扱い性
を考慮して30℃以上とし、より好ましくは40℃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℃、より好ましくは80℃以下
である。これは、融点が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、基体上に形成して使用する
場合に基体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してのことである。Here, the electrically insulating organic substance is an organic substance that is solid at least at room temperature. The melting point is set to be 30°C or higher, more preferably 40°C or higher, taking into consideration the normal usage environment and ease of handling. The upper limit of the melting point is not particularly specified, but
Practically, the temperature is about 100°C, more preferably 80°C or less. This is done considering the following considerations: even if the melting point is too high, extra energy will be consumed for heating, and when forming on a substrate, it must not exceed the heat-resistant temperature of the material generally used as the substrate. That's what it means.
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、ノナデカンからへ;1−サコンタンに
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、綿ロウ等の植物ロ
ウ、ミツロウ等の動物ロウ、オヅケライト、およびパラ
フィンロウ、微晶し1つ1ペトロラタム等の石油ロウ等
が挙げられる。これらの14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 1-sacontane. Examples of waxes include vegetable waxes such as carnauba wax and cotton wax, animal waxes such as beeswax, ozucerite, paraffin wax, and petroleum waxes such as microcrystalline petrolatum. These 14 materials have a dielectric constant ε of 1.9 to
It is a dielectric material of about 2.3.
さらには、ポリエチレン、ポリアクリルアミドや、ポリ
n−ステアリルアクリレート、ポリnステアリルメタク
リレート等のポリアクリレートのホモポリマーあるいは
コポリマー(例えばコポ17 n−ステアリルアクリレ
ートエチルメタクリレート等)等の側鎖に長いアルキル
基を有する結晶性高分子も使用可能であるが、加熱時の
粘度等を考慮すると先のパラフィン類1 ロウ類が好適
である。Furthermore, polyethylene, polyacrylamide, and homopolymers or copolymers of polyacrylates such as poly n-stearyl acrylate and poly n-stearyl methacrylate (e.g., Copo 17 n-stearyl acrylate ethyl methacrylate, etc.) have long alkyl groups in their side chains. Although crystalline polymers can also be used, the above-mentioned paraffins 1 and waxes are preferable in consideration of viscosity upon heating.
また、上記電気絶縁性有機物ζこ分散される着色剤とし
ては、従来公知の無機顔料、有機顔料、染料おびこれら
の混合物が使用できる。Further, as the colorant to be dispersed in the electrically insulating organic substance ζ, conventionally known inorganic pigments, organic pigments, dyes, and mixtures thereof can be used.
たとえば無機顔料としては、クロム系顔料、カドミウム
系顔料、鉄系顔料、コバルト系顔ネ4、群青、紺青等が
挙げられる。また、有機顔料や染料としては、ハンザイ
エロー(C,1,1)680)、ベンジジンイエローG
(C,1,21090)、ヘンジジンオレンジ(C,
1,21)10)、ファーストレッド(C,I 、37
(185)、ブリリアントカーミツ3 B (C,1,
16015−Lake)、フクロシアニンブルー (C
,1,74160)、ビクトリアブルー(C,1,42
595−Lake) 、スピリットブラック(C,1,
50415) 、オイルブルー(C,1,74350)
、アルカリブルー(C,1,4277OA) 、ファー
ストスカーレノト(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) 、カーボンブランク等が
挙げられる。Examples of inorganic pigments include chromium pigments, cadmium pigments, iron pigments, cobalt pigments, ultramarine blue, and navy blue. In addition, organic pigments and dyes include Hansa Yellow (C, 1, 1) 680), Benzidine Yellow G
(C, 1, 21090), Hengejin Orange (C,
1,21) 10), Fast Red (C,I, 37
(185), Brilliant Karmitsu 3 B (C, 1,
16015-Lake), Fuclocyanine Blue (C
, 1,74160), Victoria Blue (C, 1,42
595-Lake), Spirit Black (C, 1,
50415), oil blue (C, 1,74350)
, Alkali Blue (C, 1,4277OA), First Scarlenote (C, 1, 12315), Rhodamine 6 B (C, 1, 45160), Rhodamine Lake (C, 1, 45160-Lake), First Sky Blue ( C, 1,74200-Lake), nigrosine (C, 1,50415), carbon blank, and the like.
これらはt独でも2種以上の混合物としても用いること
ができ、所望の発色を有するものを選択して使用すれば
よい。These can be used alone or as a mixture of two or more types, and those having the desired color development may be selected and used.
現像剤には、これら電気絶縁性有機物や着色剤のほか、
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、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、ポリエステル系樹脂、ポ
リカーボネート系樹脂、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。In addition to these electrically insulating organic substances and colorants, the developer contains
A resin may be used in combination for the purpose of improving dispersibility and fixing properties of the colorant. As such resin, known materials can be selected and used as appropriate; examples include butadiene rubber,
Rubbers such as styrene-butadiene rubber, cyclized rubber, and natural rubber; synthetic resins such as styrene resins, vinyltoluene resins, acrylic resins, methacrylic resins, polyester resins, polycarbonate resins, and polyvinyl acetate resins. , rosin resins, hydrogenated rosin resins, alkyd resins containing modified alkyds such as linseed oil modified alkyd resins, and natural resins such as polyterpenes.
その他、フェノール樹JIWffl、フェノールホルマ
リン樹脂等のi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有用であるし、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類、2−エチルへ
キシルメタクリレート、ラウリルメタクリレート、ステ
アリルメタクリレート、ラウリルアクリレ−1・、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系
モノマーの重合体もしくはそれらと他の重合性七ツマ−
との共重合体ji (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−1・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 such as JIWffl, phenol-formalin resin, pentaerythritol phthalate, coumaron-indene resins, ester gum resins, and vegetable oil polyamide resins are also useful, and polyvinyl chloride and chlorine halogenated hydrocarbon polymers such as polypropylene, vinyltoluene-butadiene,
Synthetic rubbers such as butadiene-isoprene, polymers of acrylic monomers with long chain alkyl groups such as 2-ethylhexyl methacrylate, lauryl methacrylate, stearyl methacrylate, lauryl acrylate-1, octyl acrylate, or these and other Polymerizable nanatsumer
Copolymers ji (for example, styrene-lauryl methacrylate copolymer, acrylic acid-lauryl methacrylate-1 copolymer, etc.), polyolefins such as polyethylene, polyterpenes, etc. can also be used.
さらに、上記現像剤にはim常は電荷供与剤が添加され
、ここで使用される現像剤もその例外ではない。使用さ
れる型間供与剤は、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。Furthermore, a charge donating agent is usually added to the developer described above, and the developer used here is no exception. The intermold donor agents used are, for example, naphthenic acid, octenoic acid,
Metal salts of fatty acids such as oleic acid, stearic acid, isostearic acid or lauric acid, metal salts of sulfosuccinates, oil-soluble sulfonic acid metal salts, phosphoric acid ester metal salts, metal salts such as abietic acid, metal aromatic carboxylic acids salts, aromatic sulfonic acid metal salts, etc.
また、着色剤の帯電電荷を向上させるために、Sin、
、A#、O,、Tie、、Zn○、Ga!Off。In addition, in order to improve the electrostatic charge of the colorant, Sin,
,A#,O,,Tie,,Zn○,Ga! Off.
I n203.GQOz、SnO,P b()z、Mg
O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。I n203. GQOz, SnO, Pb()z, Mg
Fine particles of metal oxide such as O or a mixture thereof may be added as a charge enhancer.
−L述の各成分の配合比であるが、着色剤は電気絶縁性
を機動の溶融状M1)に対して0.01〜100gであ
ることが好ましく、より好ましくは0.1〜10gであ
る。また電荷供与剤は同じ<2に対して通常0.001
〜10g、好ましくは0.01〜1g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。Regarding the blending ratio of each component described in -L, the coloring agent is preferably 0.01 to 100 g, more preferably 0.1 to 10 g, based on the molten M1) for electrical insulation. . In addition, the charge donor is usually 0.001 for the same <2
-10g, preferably 0.01-1g. 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.
…■述の現像剤を導電性を有する基体に保持させて静電
潜像現像用現像材とするわけであるが、以下各実施例の
構成を説明する。The developer described in (1) is held on a conductive substrate to form a developer for developing an electrostatic latent image, and the structure of each example will be explained below.
第1図は1)本発明を適用した現像材のうち最も単純な
構成を有ずろものであって、それ自体が導電性を有する
シート状の導電性基体(1)上に先の現像剤(2)を全
面に塗布したものである。FIG. 1 shows 1) the one having the simplest structure among the developing materials to which the present invention is applied, in which the previous developer ( 2) is applied to the entire surface.
導電性基体(1)の材質は、この場合には導電性を有す
る必要があり、したがってたとえばAI。The material of the conductive substrate (1) needs to be conductive in this case and is therefore, for example, AI.
Cu、ステンレス、Ni、NiCr、Ag等の金属や、
導電性セラミクス、カーボン、5iC1■To (In
dium Tin 0xide) 、S n O2、さ
らには導電性高分子等が使用される。Metals such as Cu, stainless steel, Ni, NiCr, Ag,
Conductive ceramics, carbon, 5iC1■To (In
(dium Tin Oxide), SnO2, conductive polymers, etc. are used.
また、基体自体が導電性を持たない場合には、第2図に
示すように1.基体(3)の表面に導電材層(4)を形
成した後、この上に現像剤(2)を形成するようにして
もよい。In addition, if the base itself does not have conductivity, 1. as shown in FIG. After forming the conductive material layer (4) on the surface of the base (3), the developer (2) may be formed thereon.
この場合、導電材層(4)は、蒸着、スパノタメ、キ等
の手法により金属等を直接膜付けすることにより形成し
てもよいし、銀ペーストのようにR電性粒子が分散され
た材料を塗布することにより形成するようにしてもよい
。In this case, the conductive material layer (4) may be formed by directly depositing a film of metal, etc., using methods such as vapor deposition, spanotame, and ki, or may be formed using a material in which R conductive particles are dispersed, such as silver paste. It may be formed by applying.
また、導電性を持たない基体(3)としては、ポリエチ
レンテレフタレート、ポリプロピし・ン、ポリカーボネ
ート、ポリアミド等の高分子フィルム、紙(天然紙1合
成紙等)、及びこれらの複合材等が使用され、通常は可
撓性を有するものが使用されるが、必ずしも可撓性をイ
fする必要はない。In addition, as the non-conductive substrate (3), polymer films such as polyethylene terephthalate, polypropylene, polycarbonate, polyamide, paper (natural paper, synthetic paper, etc.), and composite materials thereof are used. Generally, a flexible material is used, but it is not necessarily necessary to have flexibility.
第3図は、多孔質よりなる基体を使用した例で、多孔質
基板(5)に現像剤(2)が含浸固化された形で保持さ
れている。この例では、多孔’![板(5)の裏面側に
導電材層(4)が形成され、導電性が確保されている。FIG. 3 shows an example in which a porous substrate is used, and the developer (2) is impregnated and held in a solidified form on the porous substrate (5). In this example, porous'! [A conductive material layer (4) is formed on the back side of the plate (5) to ensure conductivity.
多孔質基板(5)は、前記現像剤(2)が染み込みIJ
るものであれば如何なるものであってもよく、天然紙1
合成紙等の紙の他、木綿、麻等に代表される植物繊維や
組、羊毛に代表される動物繊維等の天然繊維、ポリアミ
ド、ポリエステル、ポリアセタール、ポリウレタン等の
有機物やガラス、セラミクス、カーボン等の無機物等よ
りなる合成繊維で作られた布、不織布等が使用可能であ
る。さらには、金属、n機高分子のメツシュや、ポリウ
レタンフォーム等の高分子発泡体等であってもよい。The porous substrate (5) is impregnated with the developer (2) and the IJ
Any paper may be used as long as it is natural paper1
In addition to paper such as synthetic paper, vegetable fibers such as cotton and hemp, natural fibers such as animal fibers such as wool, organic materials such as polyamide, polyester, polyacetal, and polyurethane, glass, ceramics, carbon, etc. Fabrics made of synthetic fibers made of inorganic materials, non-woven fabrics, etc. can be used. Furthermore, it may be a metal, an n-machine polymer mesh, a polymer foam such as polyurethane foam, or the like.
この現像剤(2)が含浸同化された多孔質基板(5)は
、第4図に示すように、導電性を有するシート状の導電
性基体(1)で裏打ちし、補強するとともに!、導電性
を確保するようにしてもよい。The porous substrate (5) in which the developer (2) has been impregnated and assimilated is lined and reinforced with a sheet-like conductive substrate (1) having conductivity, as shown in FIG. , conductivity may be ensured.
さらには、第5図に示すように、現像剤(2)が含浸固
化された多孔質基板(5)を導電材層(4)が設けられ
た基体(3)と積層するようにL7てもよい。Furthermore, as shown in FIG. 5, the porous substrate (5) impregnated and solidified with the developer (2) is laminated with the base (3) provided with the conductive material layer (4) at L7. good.
また、基体に保持される現像剤を複数色に対応したもの
となし、各色領域を一基体上に塗り分けて形成するよう
にしてもよい。Alternatively, the developer held on the substrate may be compatible with a plurality of colors, and each color region may be formed by separately painting on one substrate.
例えば第6図は、導電材層(4)が形成された基体(3
)トにイエロー色の現像剤層Y、マゼンタ色の現像剤層
M、シアン色の現像剤層Cを形成したもので、フルカラ
ー画像形成を可能とするものである。なお、フルカラー
画像形成する場合、先のイエロー色、マゼシタ色、シア
ン色の他、黒色の現像剤層の領域を必要に応じて付加し
てもよい。For example, FIG. 6 shows a substrate (3) on which a conductive material layer (4) is formed.
) A yellow developer layer Y, a magenta developer layer M, and a cyan developer layer C are formed on the top, making it possible to form a full-color image. In addition, when forming a full-color image, in addition to the above-mentioned yellow, mazeshita, and cyan colors, a black developer layer region may be added as necessary.
同様に、第7図に示すように、導電jtA層(4)が形
成された基体(3)に積層された多孔質基体(5)に対
してもイエロー色の現像剤Y、マゼンタ色の現像剤M、
シアン色の現像剤Cを各領域毎に含浸同化してもよく、
勿論第8図に示すように、これらイエロー色の現像剤Y
、マゼンク色の現像剤M。Similarly, as shown in FIG. 7, yellow developer Y and magenta developer are applied to the porous substrate (5) laminated on the substrate (3) on which the conductive jtA layer (4) is formed. agent M,
A cyan developer C may be impregnated and assimilated in each region,
Of course, as shown in FIG.
, Mazenk color developer M.
シアン色の現像剤Cが含浸同化された多孔質基体(5)
をそのまま静電潜像現像用現像材として扱うこともでき
る。ただし、後者の場合、多孔質基体(5)の裏面に導
電材層(4)を形成し導電性を確保する必要がある。Porous substrate impregnated with cyan developer C (5)
can also be used as is as a developer for developing electrostatic latent images. However, in the latter case, it is necessary to form a conductive material layer (4) on the back surface of the porous substrate (5) to ensure conductivity.
ところで、前述のように同一基体上に複数色の現像剤領
域を形成した場合、特に加熱溶融時に混色が起こる可能
性がある。By the way, when developer regions of a plurality of colors are formed on the same substrate as described above, there is a possibility that color mixing may occur particularly during heating and melting.
そこで、例えば第9図に示すように、各色の現像剤Y、
M、Cよりなる領域間に混色防止層(6)を設けるよう
にしてもよい。Therefore, as shown in FIG. 9, for example, the developer Y of each color,
A color mixture prevention layer (6) may be provided between the M and C regions.
この混色防止IN(6)は、屯なるスペーシングの役割
を果たすものであ4つば如何なるものであってもよいが
、特に吸液性祠14 (例えば1j1)述の多孔質基体
(5)と同様の4A1)1 )や18液性材l:I等を
使用するごとが好ましい。This color mixture prevention IN (6) plays the role of spacing and may be of any type, but is particularly suitable for use with the porous substrate (5) described in the liquid-absorbing shrine 14 (for example, 1j1). It is preferable to use similar 4A1)1) or 18 liquid material l:I.
また、第7図あるいは第8図に示すように、多孔質1.
v体(5)に各色の現像剤Y、 M、 Cを含浸固化
した場合、これら各色の現像剤領域を所定間隔をもって
形成すれば、各領域間の多孔質基体(5a)が!j’f
3[!m混色防止層して機能することになる。Moreover, as shown in FIG. 7 or FIG. 8, porous 1.
When the V body (5) is impregnated and solidified with the developers Y, M, and C of each color, if the developer regions of each color are formed at predetermined intervals, the porous substrate (5a) between each region is formed! j'f
3[! It functions as a color mixture prevention layer.
前述の静電潜像現像用現像材を用いて静電潜像の現像を
行うには、次のような手法によればよい。The following method may be used to develop an electrostatic latent image using the above-mentioned developer for developing an electrostatic latent image.
以ド、第2図に示す実施例のものを例にして静電潜像の
現像方法を説明する。Hereinafter, a method of developing an electrostatic latent image will be explained using the embodiment shown in FIG. 2 as an example.
感光基材(7)は、第9図に示すように、例えばシート
状の基体(7a)の上に感光層(7b)が形成されてな
るもので、当該感光層f7b)には、帯電工程及び露光
工程により画像情報に応したマイナス電荷の潜像が形成
される。As shown in FIG. 9, the photosensitive substrate (7) is formed by forming a photosensitive layer (7b) on, for example, a sheet-like substrate (7a), and the photosensitive layer (7b) is subjected to a charging process. A latent image of negative charge corresponding to the image information is formed by the exposure step.
ここで、本実施例の現像+Aにより前記マイナス電(1
;fの潜像が形成さね涜感光基材(7)を現像するには
1.現像剤(2)が感光層(7b)と接触するように車
ね合わせ、加熱1段を設けた1コール(8)によって押
圧しながら送り出すだけで良い。Here, the negative charge (1
To develop the photosensitive substrate (7) on which a latent image of f is formed: 1. It is sufficient to simply align the wheels so that the developer (2) comes into contact with the photosensitive layer (7b), and send it out while being pressed by a single call (8) provided with one heating stage.
このように現仰1f’!(2) と感光層(71′l
)とを接触さ・已ロール(8) L::J、って加熱す
ると、前記現像剤(2)が液状とな・′ツ、当該現像剤
(2)に含まれる着色剤(9)がンイ十ノ、電荷のある
部位に向か−、て床動じ付着する。しかる後、不要部分
に付着した着色剤(9)を除去し、除電工程、定着工程
等を経ることで、感光基材(7)上に画像が形成される
。In this way, the truth is 1f'! (2) and photosensitive layer (71'l
) When the roll (8) L::J is heated, the developer (2) becomes liquid and the colorant (9) contained in the developer (2) is heated. Then move towards the charged area and attach it to the floor. Thereafter, an image is formed on the photosensitive substrate (7) by removing the colorant (9) adhering to unnecessary portions and performing a static elimination process, a fixing process, etc.
なお、現像に際して、感光基材(7)と現像剤(2)と
が接触後直ちに固化すると画像品位を低下する虞れがあ
るため、感光基材(7)自体、あるいは感光基材(7)
を固定するステージ等にも加熱手段を設り加温すること
が好ましい。In addition, during development, if the photosensitive substrate (7) and the developer (2) solidify immediately after contact, there is a risk of degrading the image quality.
It is preferable that a heating means is also provided on the stage etc. on which the material is fixed to heat it.
また、基体(3)に導電材層(4)が形成されることか
ら、この>5電+4’f?M(4) ニ直)ん電a(1
0)全接続し、現像の際にバイアス電圧を印加すること
ができる。Moreover, since the conductive material layer (4) is formed on the base (3), this >5 electric +4'f? M(4)
0) All connections can be made and a bias voltage can be applied during development.
このバイアス電圧を印加すると、静電潜像の相対的な電
位をコントロールすることができ、着色材(9)の静電
潜像への付着の度合をコントロールすることができる。By applying this bias voltage, the relative potential of the electrostatic latent image can be controlled, and the degree of adhesion of the coloring material (9) to the electrostatic latent image can be controlled.
前記導電材層(4)には、バイアス電圧を印加すると同
時に交流電圧を印加し、それ自体を発熱体として利用す
ることで、ロール(8)の加熱手段を省略することもで
きる。また、当該導電材層(4)は、金属等の熱伝導性
の良いもので形成されることから、現像剤(2)に対す
る加熱温度が均一になり、この点でも有利である。The heating means for the roll (8) can be omitted by applying an AC voltage to the conductive material layer (4) at the same time as applying a bias voltage, and using the conductive material layer itself as a heating element. Further, since the conductive material layer (4) is formed of a material with good thermal conductivity such as metal, the heating temperature for the developer (2) becomes uniform, which is also advantageous.
実際、本発明者等が前述の如きシート状の現像材を作製
し、静電潜像の現像を試みたところ、解像度、精彩度に
優れ、銀塩写真に匹敵する良好な画像が安定して得られ
た。In fact, when the present inventors produced a sheet-like developing material as described above and attempted to develop an electrostatic latent image, they were able to stably produce images with excellent resolution and sharpness, comparable to silver halide photography. Obtained.
以」−5本発明の実施例について説明したが、本発明が
これら実施例に限定されるものでないことは当然であり
、本発明の要旨を逸脱しない範囲での材料、形状等の変
更が可能である。5 Examples of the present invention have been described, but it goes without saying that the present invention is not limited to these examples, and changes in materials, shapes, etc. can be made without departing from the gist of the present invention. It is.
静電潜像を現像すれば、湿式現像法と同様の画像品位を
得ることができ、使用後にはそのまま廃棄できる等、廃
棄物処理の観点等からも好適である。If an electrostatic latent image is developed, it is possible to obtain the same image quality as the wet development method, and it is suitable from the viewpoint of waste disposal, such as being able to be disposed of as is after use.
さらには、本発明の静電潜像現像用現像材においては基
体が導電性を有することから、現像に際してバイアス電
圧を印加することができ、画像の濃度1階調性1色バラ
ンス等を調整することができる。Furthermore, in the developing material for developing electrostatic latent images of the present invention, since the substrate has conductivity, a bias voltage can be applied during development, and the density, single gradation, single color balance, etc. of the image can be adjusted. be able to.
また、基体を導電性とすることで、外的な加熱手段の省
略を図ったり、加熱温度を均一にすることができる等、
付帯的なメリットも大きい。In addition, by making the base conductive, external heating means can be omitted, heating temperature can be made uniform, etc.
There are also great additional benefits.
以上の説明からも明らかなように、本発明の静電潜像現
像用現像材は、基体に現像剤を保持させたものであるの
で、例えば昇華性インクリボン等と同様極めて取り扱い
性に優れたものであり、現像操作や現像装置の大幅な簡
略化を図ることが可能である。As is clear from the above description, the developer material for developing electrostatic latent images of the present invention has a developer retained in the base material, so it is extremely easy to handle, similar to, for example, sublimation ink ribbons. Therefore, it is possible to greatly simplify the developing operation and the developing device.
また、本発明の静電潜像現像用現像材を用いてFurthermore, using the developer material for developing electrostatic latent images of the present invention,
第1図は導電性基体を用いた実施例を示す要部拡大断面
図であり、第2図は導電)イ層ををする基体を用いた実
施例の要部拡大断面図、第3図は多孔質基体を用い導電
材層を形成した実施例を示す要部拡大断面図、第4図は
多孔質基体に導電性基体を裏打ちした実施例を示す要部
拡大断面図、第5図は多孔質基体に導電材層を有する基
体を裏打ちした実施例を示す要部拡大断面図である。
第6図は導電材層を有する基体上に複数の現像剤?ij
i域を形成した実施例を示す要部拡大断面図であり、第
7図は導電材層を有する基体を裏打ちした多孔質基体に
複数の現像剤領域を形成した実施例を示す要部拡大断面
図、第8図は複数の現像剤領域が形成された多孔質基体
に導電材層を設は現像材とした実施例を示す要部拡大断
面図、第9図は混色防止層を設けた実施例を示す要部拡
大断面図である。
第1O図は本発明の現像材による静電潜像の現像方法を
説明する模式図である。
■・・・導電性基体
2・・・現像剤
3・・・多孔質基体
4・・・導電材層
6・・・混色防止層
第1図
第2図
ぢ
第3図
ぢFIG. 1 is an enlarged sectional view of the main part of an embodiment using a conductive substrate, FIG. 2 is an enlarged sectional view of the main part of an embodiment using a substrate with a conductive layer, and FIG. FIG. 4 is an enlarged sectional view of the main part showing an example in which a conductive material layer is formed using a porous substrate. FIG. 4 is an enlarged sectional view of the main part showing an example in which a porous substrate is lined with a conductive material layer. FIG. 2 is an enlarged cross-sectional view of a main part showing an example in which a solid substrate is lined with a substrate having a conductive material layer. Figure 6 shows multiple developers on a substrate having a conductive material layer? ij
FIG. 7 is an enlarged cross-sectional view of a main part showing an example in which an i-area is formed, and FIG. Figure 8 is an enlarged cross-sectional view of main parts showing an example in which a conductive material layer is provided on a porous substrate in which a plurality of developer regions are formed and a developer material is used, and Figure 9 is an embodiment in which a color mixing prevention layer is provided. FIG. 2 is an enlarged sectional view of a main part showing an example. FIG. 1O is a schematic diagram illustrating a method of developing an electrostatic latent image using the developing material of the present invention. ■...Conductive substrate 2...Developer 3...Porous substrate 4...Conductive material layer 6...Color mixture prevention layer Figure 1 Figure 2 Figure 3
Claims (3)
変化する電気絶縁性有機物に着色剤が分散されてなる現
像剤が導電性を有する基体に保持されていることを特徴
とする静電潜像現像用現像材。(1) An electrostatic latent image characterized in that a developer comprising a coloring agent dispersed in an electrically insulating organic substance that is solid at least at room temperature and changes into a solid-liquid upon heating and cooling is held on an electrically conductive substrate. Developing material for development.
像剤が領域を異にして導電性を有する基体に保持されて
いることを特徴とする請求項1記載の静電潜像現像用現
像材。(2) A developer for developing an electrostatic latent image according to claim 1, characterized in that a plurality of developers in which colorants of different color development are dispersed are held on a conductive substrate in different areas. Material.
ことを特徴とする請求項2記載の静電潜像現像用現像材
。(3) The developer for developing an electrostatic latent image according to claim 2, further comprising a color mixture prevention layer formed between the developer in each region.
Priority Applications (6)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP63156849A JP2674106B2 (en) | 1988-06-27 | 1988-06-27 | Developer for electrostatic latent image development |
CA000603237A CA1335047C (en) | 1988-06-27 | 1989-06-19 | Electrophotographic process |
DE68918996T DE68918996T2 (en) | 1988-06-27 | 1989-06-23 | Electrophotographic process. |
EP89111483A EP0348844B1 (en) | 1988-06-27 | 1989-06-23 | Electrophotographic process |
KR1019890008780A KR0138118B1 (en) | 1988-06-27 | 1989-06-26 | Electrography dealing process |
US07/869,888 US5229235A (en) | 1988-06-27 | 1992-04-14 | Electrophotographic process using melted developer |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP63156849A JP2674106B2 (en) | 1988-06-27 | 1988-06-27 | Developer for electrostatic latent image development |
Publications (2)
Publication Number | Publication Date |
---|---|
JPH026965A true JPH026965A (en) | 1990-01-11 |
JP2674106B2 JP2674106B2 (en) | 1997-11-12 |
Family
ID=15636721
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP63156849A Expired - Fee Related JP2674106B2 (en) | 1988-06-27 | 1988-06-27 | Developer for electrostatic latent image development |
Country Status (1)
Country | Link |
---|---|
JP (1) | JP2674106B2 (en) |
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5352557A (en) * | 1992-12-11 | 1994-10-04 | Fuji Xerox Co., Ltd. | Liquid developer for electrostatic photography |
US5529874A (en) * | 1993-05-07 | 1996-06-25 | Fuji Xerox Co., Ltd. | Liquid developer for electrophotography |
US5622804A (en) * | 1994-05-30 | 1997-04-22 | Fuji Xerox Co., Ltd. | Liquid developer for electrophotography, process for producing the same, and process for image formation using the same |
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 JP63156849A patent/JP2674106B2/en not_active Expired - Fee Related
Cited By (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5723250A (en) * | 1909-05-30 | 1998-03-03 | Fuji Xerox Co., Ltd. | Process for image formation using liquid developer |
US5352557A (en) * | 1992-12-11 | 1994-10-04 | Fuji Xerox Co., Ltd. | Liquid developer for electrostatic photography |
US5529874A (en) * | 1993-05-07 | 1996-06-25 | Fuji Xerox Co., Ltd. | Liquid developer for electrophotography |
US5622804A (en) * | 1994-05-30 | 1997-04-22 | Fuji Xerox Co., Ltd. | Liquid developer for electrophotography, process for producing the same, and process for image formation using the same |
US5783350A (en) * | 1995-12-14 | 1998-07-21 | Fuji Xerox Co., Ltd. | Developer for electrostatic photography and image forming method |
Also Published As
Publication number | Publication date |
---|---|
JP2674106B2 (en) | 1997-11-12 |
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