JPH03200266A - Liquid developer for electrostatic charge image - Google Patents
Liquid developer for electrostatic charge imageInfo
- Publication number
- JPH03200266A JPH03200266A JP1342245A JP34224589A JPH03200266A JP H03200266 A JPH03200266 A JP H03200266A JP 1342245 A JP1342245 A JP 1342245A JP 34224589 A JP34224589 A JP 34224589A JP H03200266 A JPH03200266 A JP H03200266A
- Authority
- JP
- Japan
- Prior art keywords
- acid amide
- solvent
- erucic acid
- added
- liquid developer
- 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
- 239000007788 liquid Substances 0.000 title claims abstract description 27
- 239000011347 resin Substances 0.000 claims abstract description 27
- 229920005989 resin Polymers 0.000 claims abstract description 27
- 239000002904 solvent Substances 0.000 claims abstract description 21
- 239000003086 colorant Substances 0.000 claims abstract description 20
- 229920001296 polysiloxane Polymers 0.000 claims abstract description 6
- 239000002245 particle Substances 0.000 claims abstract description 4
- YCKRFDGAMUMZLT-UHFFFAOYSA-N Fluorine atom Chemical compound [F] YCKRFDGAMUMZLT-UHFFFAOYSA-N 0.000 claims abstract description 3
- 229910052731 fluorine Inorganic materials 0.000 claims abstract description 3
- 239000011737 fluorine Substances 0.000 claims abstract description 3
- -1 erucic acid amide compound Chemical class 0.000 claims description 23
- 150000001338 aliphatic hydrocarbons Chemical class 0.000 claims description 4
- UAUDZVJPLUQNMU-KTKRTIGZSA-N erucamide Chemical compound CCCCCCCC\C=C/CCCCCCCCCCCC(N)=O UAUDZVJPLUQNMU-KTKRTIGZSA-N 0.000 abstract description 14
- 229930195733 hydrocarbon Natural products 0.000 abstract description 7
- 150000002430 hydrocarbons Chemical class 0.000 abstract description 7
- 239000000203 mixture Substances 0.000 abstract description 7
- 239000004215 Carbon black (E152) Substances 0.000 abstract description 6
- 239000011230 binding agent Substances 0.000 abstract description 4
- 230000003247 decreasing effect Effects 0.000 abstract 1
- 230000003311 flocculating effect Effects 0.000 abstract 1
- 238000004519 manufacturing process Methods 0.000 description 16
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 15
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 14
- 239000000049 pigment Substances 0.000 description 13
- 238000011010 flushing procedure Methods 0.000 description 12
- 238000000034 method Methods 0.000 description 10
- 239000004698 Polyethylene Substances 0.000 description 8
- 229920000573 polyethylene Polymers 0.000 description 8
- 239000004021 humic acid Substances 0.000 description 7
- QJZYHAIUNVAGQP-UHFFFAOYSA-N 3-nitrobicyclo[2.2.1]hept-5-ene-2,3-dicarboxylic acid Chemical compound C1C2C=CC1C(C(=O)O)C2(C(O)=O)[N+]([O-])=O QJZYHAIUNVAGQP-UHFFFAOYSA-N 0.000 description 6
- 239000000243 solution Substances 0.000 description 6
- 229910052710 silicon Inorganic materials 0.000 description 5
- 238000010438 heat treatment Methods 0.000 description 4
- 238000004898 kneading Methods 0.000 description 4
- 239000000463 material Substances 0.000 description 4
- 239000003921 oil Substances 0.000 description 4
- 239000012188 paraffin wax Substances 0.000 description 4
- 235000019809 paraffin wax Nutrition 0.000 description 4
- 235000019271 petrolatum Nutrition 0.000 description 4
- 239000000126 substance Substances 0.000 description 4
- CNPVJWYWYZMPDS-UHFFFAOYSA-N 2-methyldecane Chemical compound CCCCCCCCC(C)C CNPVJWYWYZMPDS-UHFFFAOYSA-N 0.000 description 3
- 239000003795 chemical substances by application Substances 0.000 description 3
- 229920001577 copolymer Polymers 0.000 description 3
- 239000000178 monomer Substances 0.000 description 3
- 239000010703 silicon Substances 0.000 description 3
- 238000012360 testing method Methods 0.000 description 3
- MYRTYDVEIRVNKP-UHFFFAOYSA-N 1,2-Divinylbenzene Chemical compound C=CC1=CC=CC=C1C=C MYRTYDVEIRVNKP-UHFFFAOYSA-N 0.000 description 2
- 229920000178 Acrylic resin Polymers 0.000 description 2
- 239000004925 Acrylic resin Substances 0.000 description 2
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 description 2
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 2
- 229910052799 carbon Inorganic materials 0.000 description 2
- 239000011248 coating agent Substances 0.000 description 2
- 238000000576 coating method Methods 0.000 description 2
- 238000004040 coloring Methods 0.000 description 2
- 230000000052 comparative effect Effects 0.000 description 2
- 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 2
- 230000000694 effects Effects 0.000 description 2
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 2
- BKIMMITUMNQMOS-UHFFFAOYSA-N nonane Chemical compound CCCCCCCCC BKIMMITUMNQMOS-UHFFFAOYSA-N 0.000 description 2
- TVMXDCGIABBOFY-UHFFFAOYSA-N octane Chemical compound CCCCCCCC TVMXDCGIABBOFY-UHFFFAOYSA-N 0.000 description 2
- RVZRBWKZFJCCIB-UHFFFAOYSA-N perfluorotributylamine Chemical compound FC(F)(F)C(F)(F)C(F)(F)C(F)(F)N(C(F)(F)C(F)(F)C(F)(F)C(F)(F)F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)F RVZRBWKZFJCCIB-UHFFFAOYSA-N 0.000 description 2
- IEQIEDJGQAUEQZ-UHFFFAOYSA-N phthalocyanine Chemical compound N1C(N=C2C3=CC=CC=C3C(N=C3C4=CC=CC=C4C(=N4)N3)=N2)=C(C=CC=C2)C2=C1N=C1C2=CC=CC=C2C4=N1 IEQIEDJGQAUEQZ-UHFFFAOYSA-N 0.000 description 2
- 229920000098 polyolefin Polymers 0.000 description 2
- 150000003839 salts Chemical class 0.000 description 2
- 229920002545 silicone oil Polymers 0.000 description 2
- 239000011734 sodium Substances 0.000 description 2
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 2
- 229920002554 vinyl polymer Polymers 0.000 description 2
- QIVUCLWGARAQIO-OLIXTKCUSA-N (3s)-n-[(3s,5s,6r)-6-methyl-2-oxo-1-(2,2,2-trifluoroethyl)-5-(2,3,6-trifluorophenyl)piperidin-3-yl]-2-oxospiro[1h-pyrrolo[2,3-b]pyridine-3,6'-5,7-dihydrocyclopenta[b]pyridine]-3'-carboxamide Chemical compound C1([C@H]2[C@H](N(C(=O)[C@@H](NC(=O)C=3C=C4C[C@]5(CC4=NC=3)C3=CC=CN=C3NC5=O)C2)CC(F)(F)F)C)=C(F)C=CC(F)=C1F QIVUCLWGARAQIO-OLIXTKCUSA-N 0.000 description 1
- QBZIEGUIYWGBMY-FUZXWUMZSA-N (5Z)-5-hydroxyimino-6-oxonaphthalene-2-sulfonic acid iron Chemical compound [Fe].O\N=C1/C(=O)C=Cc2cc(ccc12)S(O)(=O)=O.O\N=C1/C(=O)C=Cc2cc(ccc12)S(O)(=O)=O.O\N=C1/C(=O)C=Cc2cc(ccc12)S(O)(=O)=O QBZIEGUIYWGBMY-FUZXWUMZSA-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
- GTJOHISYCKPIMT-UHFFFAOYSA-N 2-methylundecane Chemical compound CCCCCCCCCC(C)C GTJOHISYCKPIMT-UHFFFAOYSA-N 0.000 description 1
- KGIGUEBEKRSTEW-UHFFFAOYSA-N 2-vinylpyridine Chemical compound C=CC1=CC=CC=N1 KGIGUEBEKRSTEW-UHFFFAOYSA-N 0.000 description 1
- DWDURZSYQTXVIN-UHFFFAOYSA-N 4-[(4-aminophenyl)-(4-methyliminocyclohexa-2,5-dien-1-ylidene)methyl]aniline Chemical compound C1=CC(=NC)C=CC1=C(C=1C=CC(N)=CC=1)C1=CC=C(N)C=C1 DWDURZSYQTXVIN-UHFFFAOYSA-N 0.000 description 1
- DBCAQXHNJOFNGC-UHFFFAOYSA-N 4-bromo-1,1,1-trifluorobutane Chemical compound FC(F)(F)CCCBr DBCAQXHNJOFNGC-UHFFFAOYSA-N 0.000 description 1
- IYHIFXGFKVJNBB-UHFFFAOYSA-N 5-chloro-2-[(2-hydroxynaphthalen-1-yl)diazenyl]-4-methylbenzenesulfonic acid Chemical compound C1=C(Cl)C(C)=CC(N=NC=2C3=CC=CC=C3C=CC=2O)=C1S(O)(=O)=O IYHIFXGFKVJNBB-UHFFFAOYSA-N 0.000 description 1
- 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 1
- 102100040440 Adenylate kinase isoenzyme 5 Human genes 0.000 description 1
- 101710168711 Adenylate kinase isoenzyme 5 Proteins 0.000 description 1
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical class N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 1
- VVAVKBBTPWYADW-UHFFFAOYSA-L Biebrich scarlet Chemical compound [Na+].[Na+].OC1=CC=C2C=CC=CC2=C1N=NC(C(=C1)S([O-])(=O)=O)=CC=C1N=NC1=CC=C(S([O-])(=O)=O)C=C1 VVAVKBBTPWYADW-UHFFFAOYSA-L 0.000 description 1
- DPUOLQHDNGRHBS-UHFFFAOYSA-N Brassidinsaeure Natural products CCCCCCCCC=CCCCCCCCCCCCC(O)=O DPUOLQHDNGRHBS-UHFFFAOYSA-N 0.000 description 1
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 1
- 241000557626 Corvus corax Species 0.000 description 1
- XDTMQSROBMDMFD-UHFFFAOYSA-N Cyclohexane Chemical compound C1CCCCC1 XDTMQSROBMDMFD-UHFFFAOYSA-N 0.000 description 1
- UAUDZVJPLUQNMU-UHFFFAOYSA-N Erucasaeureamid Natural products CCCCCCCCC=CCCCCCCCCCCCC(N)=O UAUDZVJPLUQNMU-UHFFFAOYSA-N 0.000 description 1
- URXZXNYJPAJJOQ-UHFFFAOYSA-N Erucic acid Natural products CCCCCCC=CCCCCCCCCCCCC(O)=O URXZXNYJPAJJOQ-UHFFFAOYSA-N 0.000 description 1
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 1
- 235000000177 Indigofera tinctoria Nutrition 0.000 description 1
- SGVYKUFIHHTIFL-UHFFFAOYSA-N Isobutylhexyl Natural products CCCCCCCC(C)C SGVYKUFIHHTIFL-UHFFFAOYSA-N 0.000 description 1
- NHTMVDHEPJAVLT-UHFFFAOYSA-N Isooctane Chemical compound CC(C)CC(C)(C)C NHTMVDHEPJAVLT-UHFFFAOYSA-N 0.000 description 1
- LTGPFZWZZNUIIK-LURJTMIESA-N Lysol Chemical compound NCCCC[C@H](N)CO LTGPFZWZZNUIIK-LURJTMIESA-N 0.000 description 1
- CERQOIWHTDAKMF-UHFFFAOYSA-M Methacrylate Chemical compound CC(=C)C([O-])=O CERQOIWHTDAKMF-UHFFFAOYSA-M 0.000 description 1
- 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 1
- 239000002174 Styrene-butadiene Substances 0.000 description 1
- 239000004234 Yellow 2G Substances 0.000 description 1
- YFCGDEUVHLPRCZ-UHFFFAOYSA-N [dimethyl(trimethylsilyloxy)silyl]oxy-dimethyl-trimethylsilyloxysilane Chemical compound C[Si](C)(C)O[Si](C)(C)O[Si](C)(C)O[Si](C)(C)C YFCGDEUVHLPRCZ-UHFFFAOYSA-N 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 229920006243 acrylic copolymer Polymers 0.000 description 1
- 239000008346 aqueous phase Substances 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 235000013871 bee wax Nutrition 0.000 description 1
- 239000012166 beeswax Substances 0.000 description 1
- MTAZNLWOLGHBHU-UHFFFAOYSA-N butadiene-styrene rubber Chemical compound C=CC=C.C=CC1=CC=CC=C1 MTAZNLWOLGHBHU-UHFFFAOYSA-N 0.000 description 1
- 229910052791 calcium Inorganic materials 0.000 description 1
- 239000011575 calcium Substances 0.000 description 1
- PZTQVMXMKVTIRC-UHFFFAOYSA-L chembl2028348 Chemical compound [Ca+2].[O-]S(=O)(=O)C1=CC(C)=CC=C1N=NC1=C(O)C(C([O-])=O)=CC2=CC=CC=C12 PZTQVMXMKVTIRC-UHFFFAOYSA-L 0.000 description 1
- ZLFVRXUOSPRRKQ-UHFFFAOYSA-N chembl2138372 Chemical compound [O-][N+](=O)C1=CC(C)=CC=C1N=NC1=C(O)C=CC2=CC=CC=C12 ZLFVRXUOSPRRKQ-UHFFFAOYSA-N 0.000 description 1
- 239000010779 crude oil Substances 0.000 description 1
- 239000004148 curcumin Substances 0.000 description 1
- 239000003085 diluting agent Substances 0.000 description 1
- JVSWJIKNEAIKJW-UHFFFAOYSA-N dimethyl-hexane Natural products CCCCCC(C)C JVSWJIKNEAIKJW-UHFFFAOYSA-N 0.000 description 1
- FTZLWXQKVFFWLY-UHFFFAOYSA-L disodium;2,5-dichloro-4-[3-methyl-5-oxo-4-[(4-sulfonatophenyl)diazenyl]-4h-pyrazol-1-yl]benzenesulfonate Chemical compound [Na+].[Na+].CC1=NN(C=2C(=CC(=C(Cl)C=2)S([O-])(=O)=O)Cl)C(=O)C1N=NC1=CC=C(S([O-])(=O)=O)C=C1 FTZLWXQKVFFWLY-UHFFFAOYSA-L 0.000 description 1
- 239000006185 dispersion Substances 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
- 229920001971 elastomer Polymers 0.000 description 1
- DPUOLQHDNGRHBS-KTKRTIGZSA-N erucic acid Chemical compound CCCCCCCC\C=C/CCCCCCCCCCCC(O)=O DPUOLQHDNGRHBS-KTKRTIGZSA-N 0.000 description 1
- STVZJERGLQHEKB-UHFFFAOYSA-N ethylene glycol dimethacrylate Substances CC(=C)C(=O)OCCOC(=O)C(C)=C STVZJERGLQHEKB-UHFFFAOYSA-N 0.000 description 1
- 238000009472 formulation Methods 0.000 description 1
- 229920000578 graft copolymer Polymers 0.000 description 1
- 229940097275 indigo Drugs 0.000 description 1
- COHYTHOBJLSHDF-UHFFFAOYSA-N indigo powder Natural products N1C2=CC=CC=C2C(=O)C1=C1C(=O)C2=CC=CC=C2N1 COHYTHOBJLSHDF-UHFFFAOYSA-N 0.000 description 1
- 238000002347 injection Methods 0.000 description 1
- 239000007924 injection Substances 0.000 description 1
- 239000001023 inorganic pigment Substances 0.000 description 1
- VKPSKYDESGTTFR-UHFFFAOYSA-N isododecane Natural products CC(C)(C)CC(C)CC(C)(C)C VKPSKYDESGTTFR-UHFFFAOYSA-N 0.000 description 1
- 235000010187 litholrubine BK Nutrition 0.000 description 1
- FDZZZRQASAIRJF-UHFFFAOYSA-M malachite green Chemical compound [Cl-].C1=CC(N(C)C)=CC=C1C(C=1C=CC=CC=1)=C1C=CC(=[N+](C)C)C=C1 FDZZZRQASAIRJF-UHFFFAOYSA-M 0.000 description 1
- 229940107698 malachite green Drugs 0.000 description 1
- 150000002688 maleic acid derivatives Chemical class 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 239000012046 mixed solvent Substances 0.000 description 1
- AYOOGWWGECJQPI-NSHDSACASA-N n-[(1s)-1-(5-fluoropyrimidin-2-yl)ethyl]-3-(3-propan-2-yloxy-1h-pyrazol-5-yl)imidazo[4,5-b]pyridin-5-amine Chemical compound N1C(OC(C)C)=CC(N2C3=NC(N[C@@H](C)C=4N=CC(F)=CN=4)=CC=C3N=C2)=N1 AYOOGWWGECJQPI-NSHDSACASA-N 0.000 description 1
- VOVZXURTCKPRDQ-CQSZACIVSA-N n-[4-[chloro(difluoro)methoxy]phenyl]-6-[(3r)-3-hydroxypyrrolidin-1-yl]-5-(1h-pyrazol-5-yl)pyridine-3-carboxamide Chemical compound C1[C@H](O)CCN1C1=NC=C(C(=O)NC=2C=CC(OC(F)(F)Cl)=CC=2)C=C1C1=CC=NN1 VOVZXURTCKPRDQ-CQSZACIVSA-N 0.000 description 1
- JMXROTHPANUTOJ-UHFFFAOYSA-H naphthol green b Chemical compound [Na+].[Na+].[Na+].[Fe+3].C1=C(S([O-])(=O)=O)C=CC2=C(N=O)C([O-])=CC=C21.C1=C(S([O-])(=O)=O)C=CC2=C(N=O)C([O-])=CC=C21.C1=C(S([O-])(=O)=O)C=CC2=C(N=O)C([O-])=CC=C21 JMXROTHPANUTOJ-UHFFFAOYSA-H 0.000 description 1
- PYUYQYBDJFMFTH-WMMMYUQOSA-N naphthol red Chemical compound CCOC1=CC=CC=C1NC(=O)C(C1=O)=CC2=CC=CC=C2\C1=N\NC1=CC=C(C(N)=O)C=C1 PYUYQYBDJFMFTH-WMMMYUQOSA-N 0.000 description 1
- CTIQLGJVGNGFEW-UHFFFAOYSA-L naphthol yellow S Chemical compound [Na+].[Na+].C1=C(S([O-])(=O)=O)C=C2C([O-])=C([N+]([O-])=O)C=C([N+]([O-])=O)C2=C1 CTIQLGJVGNGFEW-UHFFFAOYSA-L 0.000 description 1
- 239000000025 natural resin Substances 0.000 description 1
- CXQXSVUQTKDNFP-UHFFFAOYSA-N octamethyltrisiloxane Chemical compound C[Si](C)(C)O[Si](C)(C)O[Si](C)(C)C CXQXSVUQTKDNFP-UHFFFAOYSA-N 0.000 description 1
- 239000012860 organic pigment Substances 0.000 description 1
- 239000003208 petroleum Substances 0.000 description 1
- 239000011164 primary particle 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
- 229920003987 resole Polymers 0.000 description 1
- 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 1
- 239000005060 rubber Substances 0.000 description 1
- 239000002002 slurry Substances 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 239000011115 styrene butadiene Substances 0.000 description 1
- 229920003048 styrene butadiene rubber Polymers 0.000 description 1
- JOUDBUYBGJYFFP-FOCLMDBBSA-N thioindigo Chemical compound S\1C2=CC=CC=C2C(=O)C/1=C1/C(=O)C2=CC=CC=C2S1 JOUDBUYBGJYFFP-FOCLMDBBSA-N 0.000 description 1
- 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 1
- KMIOJWCYOHBUJS-HAKPAVFJSA-N vorolanib Chemical compound C1N(C(=O)N(C)C)CC[C@@H]1NC(=O)C1=C(C)NC(\C=C/2C3=CC(F)=CC=C3NC\2=O)=C1C KMIOJWCYOHBUJS-HAKPAVFJSA-N 0.000 description 1
- 239000001993 wax Substances 0.000 description 1
- 235000019235 yellow 2G Nutrition 0.000 description 1
Landscapes
- Liquid Developers In Electrophotography (AREA)
Abstract
Description
【発明の詳細な説明】
(産業上の分野)
本発明は、電子写真、静電記録、静電印刷等に用いられ
る熱ロール定着用の液体現像剤に関する。DETAILED DESCRIPTION OF THE INVENTION (Industrial Field) The present invention relates to a liquid developer for hot roll fixing used in electrophotography, electrostatic recording, electrostatic printing, and the like.
[従来の技術1
熱ロール定着ロール用の液体現像剤として、特開昭63
−301966〜301969号公報、同64−500
62〜50067号、同64−52167号、同64−
142560〜142561号公報などがある。これら
は脂肪族炭化水素が主成分の担体液のため、その脂肪族
炭化水素のガスが複写機外に排出される、定着ロールに
塗布するためのシリコンオイルを供給しなければならず
、そのために複写機が複雑になったり、消耗品点数が増
すなどの問題があった。[Prior art 1: As a liquid developer for a heat roll fixing roll,
-301966 to 301969, 64-500
No. 62-50067, No. 64-52167, No. 64-
142560-142561, etc. Since these are carrier liquids mainly composed of aliphatic hydrocarbons, the aliphatic hydrocarbon gas is discharged outside the copying machine, and silicone oil must be supplied to apply to the fixing roll. There were problems such as the copying machine becoming more complex and the number of consumables increasing.
[本発明の目的1
複写機から発生する炭化水素系の溶剤ガスの低減を目的
とする。[Objective 1 of the present invention] An object of the present invention is to reduce hydrocarbon solvent gas generated from a copying machine.
液体現像剤を使用した熱ロール定着装置において、定着
ロールへのオイル塗布装置の除去を可能とし、またオイ
ル供給の手間を省く。To make it possible to remove an oil application device to a fixing roll in a hot roll fixing device using a liquid developer, and to save the trouble of oil supply.
不燃性の液剤をある割合で混入させることにより引火な
どの危険を少なくする。By mixing in a certain proportion of nonflammable liquid, the risk of ignition is reduced.
]発明の構成】
近年、熱効率が高く高速定着が可能な液体現像剤の定着
方法として、熱ロール定着が提案されている。担体液(
こ炭化水素系の溶剤を使用し、この定着方法採用すると
、従来より使用されている雰囲気定着に比べ、若干単位
枚数あたりの溶剤ガス排出量が減少するが、高速で多数
枚複写をしたときには大量の溶剤ガスが発生する。また
、トナー層と定着ロールとの離型性を上げるためシリコ
ンオイルの塗布が必要であった。本発明は、担体液とし
てフッ素系溶剤を含有させることにより、上記欠点を改
良するとともに、トナーの凝集力を上げ、いわゆる″ホ
ットオフセット°ゝを防止する点にある。[Structure of the Invention] In recent years, hot roll fixing has been proposed as a method for fixing liquid developers that has high thermal efficiency and enables high-speed fixing. Carrier liquid (
By using this hydrocarbon solvent and adopting this fixing method, the amount of solvent gas emitted per unit number of sheets is slightly reduced compared to the conventional atmosphere fixing method, but when copying a large number of sheets at high speed, a large amount of gas is emitted. of solvent gas is generated. Furthermore, it was necessary to apply silicone oil to improve the releasability between the toner layer and the fixing roll. The present invention aims to improve the above-mentioned drawbacks, increase the cohesive force of the toner, and prevent so-called "hot offset" by containing a fluorine-based solvent as a carrier liquid.
本発明に使用されるフッ素系の溶剤としては、フロリナ
ートFC−77、FC−40、FC−43、FC−70
(以上住人3M社’JJ> 、アフルード、E−10,
E−16、E−18(以上旭硝子社製)等が挙げられる
。また、同時に使用されてもよいシリコーン系の溶剤と
しては、KF96(信越シリコン)、5H200%5l
−1344(東しシリコン)、TSF451 (東芝
シリコン)などが挙げられ、その他デカメチルテトラシ
ロキサン、オクタメチルトリシロキサン等を使用しても
よい。また、脂肪族炭化水素溶液としてシクロヘキサン
、n−ヘキサン、n−へブタン、n−オクタン、n−ノ
ナン、イソオクタン、イソドデカン、リグロイン及びそ
れらの混合物などの石油系炭化水素(市販品としてエク
ソンケミカル社製アイソパーE、G、H,L、に、Vや
シェル石油社製シェルゾール71.ソルッペッソ150
、等がある)が挙げられこれらを適宜混合して使用する
。転写用剤を低減するために、担体液は1ocst以下
、好ましくは3cst以下がよい。Fluorinated solvents used in the present invention include Fluorinert FC-77, FC-40, FC-43, FC-70
(3M Company'JJ>, Afroud, E-10,
Examples include E-16 and E-18 (all manufactured by Asahi Glass Co., Ltd.). In addition, examples of silicone-based solvents that may be used at the same time include KF96 (Shin-Etsu Silicon), 5H200% 5L
-1344 (Toshiba Silicon), TSF451 (Toshiba Silicon), etc., and decamethyltetrasiloxane, octamethyltrisiloxane, etc. may also be used. In addition, as an aliphatic hydrocarbon solution, petroleum hydrocarbons such as cyclohexane, n-hexane, n-hebutane, n-octane, n-nonane, isooctane, isododecane, ligroin, and mixtures thereof (commercially available products manufactured by Exxon Chemical Co., Ltd. Isopar E, G, H, L, V and Shell Oil Co., Ltd. Shell Sol 71. Solupesso 150
, etc.), and these may be mixed and used as appropriate. In order to reduce the transfer agent, the carrier liquid should be 1 ocst or less, preferably 3 cst or less.
本発明においてはトナーの凝集力を上げる手段としてエ
ルカ酸アミド化合物を添加使用するものである。In the present invention, an erucic acid amide compound is added as a means for increasing the cohesive force of the toner.
本発明の静電写真用液体現像剤は着色剤及び結着樹脂か
ら構成されるトナー粒子をシリコーン系溶剤を主成分と
する担体液中に分散させてなる現像液中にエルカ酸アミ
ド化合物を添加含有せしめたものであり、必要に応じ極
性制御剤などが更に添加して構成されている。The electrostatic photographic liquid developer of the present invention has an erucic acid amide compound added to a developer prepared by dispersing toner particles composed of a colorant and a binder resin in a carrier liquid mainly composed of a silicone solvent. A polarity control agent and the like may be further added as necessary.
エルカ酸アミド化合物は下記式
%式%)
を有するものであり、液体現像剤100重量部に対し0
.01−10重量部好ましくは0.1〜5重量部の範囲
で添加される。The erucic acid amide compound has the following formula:
.. It is added in an amount of 0.1 to 10 parts by weight, preferably 0.1 to 5 parts by weight.
電p写真用液体現像剤にエルカ酸アミド化合物が添加さ
れていると、エルカ酸アミド化合物がトナー粒子に吸着
されたり分散溶媒(担体w1)に溶解したりして、金属
製加熱定着ローラに対し剥離剤、耐ブロツキング特性と
して作用するようになり、その結果、トナーが定着ロー
ラに付着しにくくなる。また、エルカ酸アミド化合物は
現像・転写特性をも向上させる効果が認められる。When an erucic acid amide compound is added to a liquid developer for electrophotography, the erucic acid amide compound is adsorbed to the toner particles or dissolved in the dispersion solvent (carrier w1), and the erucic acid amide compound is attached to the metal heating fixing roller. It acts as a release agent and anti-blocking property, making it difficult for toner to adhere to the fixing roller. Furthermore, the effect of the erucic acid amide compound in improving the development and transfer characteristics is also recognized.
本発明に使用する着色材としては、プリンテックスV、
プリンテックスU、プリンテックスG、スペシャルブラ
ック15、スペシャルブラック4、スペシャルブラック
4−B(以上デグサ社製)、三菱#44、#30、MR
−11%MA−100(以上三菱化成社製)、シーベン
1035.ラーベン1252.ニュースペクト■ (以
上コロンビアカーボン社製)、リーガル400.660
、ブラックバール900.1100,1300、モーガ
ルしく以上キャボット社!81)などの無機顔料および
フタロシアニンブルー、フタロシアニングリーン、スカ
イブルー、ローダミンレーキ、マラカイトグリーンレー
キ、メチルバイオレットレーキ、ピーコックブルーレー
キ、ナフトールグリーンB、ナフトールグリーンY、ナ
フトールイエローS、ナフトールレッド、リソールファ
ーストイエロー2G、パーマネントレッド4R,ブリリ
アントファーストスカーレット、ハンザイエロー、ベン
ジジンイエロー、リソールレッド、レーキレッドCル−
キレッドD1ブリリアントカーミン6B、パーマネント
レッドF5R、ビグメントスカーレット3Bインジゴ、
チオインジゴオイルピンクおよびボルドー10Bなどの
有機顔料があげられる。The coloring materials used in the present invention include Printex V,
Printex U, Printex G, Special Black 15, Special Black 4, Special Black 4-B (manufactured by Degussa), Mitsubishi #44, #30, MR
-11% MA-100 (manufactured by Mitsubishi Chemical Corporation), Sieben 1035. Raven 1252. New Spect■ (manufactured by Columbia Carbon), Regal 400.660
, Black Bar 900, 1100, 1300, Mogul and more Cabot! 81) and inorganic pigments such as Phthalocyanine Blue, Phthalocyanine Green, Sky Blue, Rhodamine Lake, Malachite Green Lake, Methyl Violet Lake, Peacock Blue Lake, Naphthol Green B, Naphthol Green Y, Naphthol Yellow S, Naphthol Red, Lysol Fast Yellow 2G , Permanent Red 4R, Brilliant First Scarlet, Hansa Yellow, Benzidine Yellow, Resole Red, Lake Red C Ru-
Killed D1 Brilliant Carmine 6B, Permanent Red F5R, Pigment Scarlet 3B Indigo,
Examples include organic pigments such as Thioindigo Oil Pink and Bordeaux 10B.
本発明においては、これら顔料を予じめ樹脂等で被覆処
理をして用いてもよい。被覆樹脂として、液体現像剤の
製造で従来より使用されていた樹脂の全てが適用し得る
。代表的なものとしては、ポリオレフィン、アクリル樹
脂、ロジン変性樹脂、スチレンブタジェン樹脂、天然樹
脂、オレフイン−アクリル共重合体、パラフィンワック
スなどがあげられる。これらは単独でも2種以上が併覆
されてもよく、更には、これらの樹脂に他の樹脂類を混
合することもできる。In the present invention, these pigments may be used after being coated with a resin or the like in advance. As the coating resin, all resins conventionally used in the production of liquid developers can be used. Typical examples include polyolefins, acrylic resins, rosin-modified resins, styrene-butadiene resins, natural resins, olefin-acrylic copolymers, and paraffin waxes. These resins may be used alone or in combination of two or more, and furthermore, other resins may be mixed with these resins.
例えばパラフィンワックス、ポリオレフィンでは次のよ
うなものをあげることができる。For example, paraffin wax and polyolefin include the following.
メーカー 銘 柄 軟化点アライド
ACポリエチレン 170285℃ケミカル
ACポリエチレン617,617A 102ACポリ
エチレン 9.9A 117ACポリエチレン43
0 60
ACポリエチレン4o595
^Cポリエチレン 40+ 102ACポリエチL
/ン540 108
ACポリエチレン58olo8
エボレン N−14105
エボレン E−1596
サンワツクス 13+−P 108サンワツクス
+51−P 107コダツク
工注化成
サンワックス 16+−P Illサンワックス
165−P 107サンワツクス +71−P
105サンワツクス E−250P 102サン
ワックスE−300P 98
純正薬品 パラフィンワックス 40−90ヘキ
スト PED 521 +04
PED 543 110PED 、1
53 98安原油脂 ニオレックスL
105ニオレツクスE 100
被覆処理としては特に、顔料を一次粒子にまで分散し、
階調性、解像力、画像濃度などを一層向上せしめるため
にフラッシング法が有効である。Manufacturer Brand Softening point Allied AC polyethylene 170285℃ Chemical
AC polyethylene 617, 617A 102AC polyethylene 9.9A 117AC polyethylene 43
0 60 AC polyethylene 4o595 ^C polyethylene 40+ 102AC polyethylene L
/n 540 108 AC polyethylene 58olo8 Evolen N-14105 Evolen E-1596 Sunwax 13+-P 108 Sunwax +51-P 107 Kodak injection chemical sunwax 16+-P Ill Sunwax
165-P 107 Sunwax +71-P
105 Sunwax E-250P 102 Sunwax E-300P 98 Genuine chemicals Paraffin wax 40-90 Hoechst PED 521 +04
PED 543 110PED, 1
53 98 cheap crude oil Niolex L
105 Niolex E 100 In particular, the coating treatment involves dispersing the pigment down to the primary particles,
A flushing method is effective for further improving gradation, resolution, image density, etc.
フラッシング法とは、顔料又は顔料の含水ペーストを樹
脂溶液又は樹脂とともにフラッシャ−と呼ばれるニーダ
−に入れよく混合しくこの過程で顔料の囲りに存在する
水が樹脂溶液又は樹脂により置換される。)、これをニ
ーダ−より取出し水相を捨て、樹脂溶液又は樹脂中に顔
料が加熱又は常温で混線分散されたものを乾燥し溶剤を
除去した後、得られた塊状物を粉砕するというものであ
る。このものを本発明においては「フラッシング顔料」
と称することにする。なお、ニーダ−で混練しながら減
圧により水、溶剤を除去するような手当が採られてもか
まわない。フラッシング処理にあたっては、顔料のみな
らず染料も水とともに泥状に練り使用することで顔料と
ほぼ同等の結果が得られることから、本発明ではフラッ
シング処理される染料もトナー成分として採用すること
が可能である。フラッシングする際の染顔料と樹脂との
割合は樹脂100重量部に対して染顔料10〜60重量
部が適当である。また、フラッシング処理はフミン酸、
フミン酸塩(Na塩、NH4塩など)又はフミン酸誘導
体の存在下に行なうのがとくに有利である。これら添加
されるフミン酸類の量は染顔料含水液の0.1〜30重
量%程度が適当である。In the flashing method, a pigment or a water-containing paste of the pigment is mixed well together with a resin solution or resin in a kneader called a flasher, and in this process, water existing around the pigment is replaced by the resin solution or resin. ), this is taken out from the kneader, the aqueous phase is discarded, the resin solution or the pigment mixed and dispersed in the resin by heating or at room temperature is dried, the solvent is removed, and the resulting lump is pulverized. be. In the present invention, this material is referred to as "flushing pigment".
I will call it . Incidentally, measures may be taken to remove water and solvent under reduced pressure while kneading with a kneader. In the flushing process, by kneading not only the pigment but also the dye into a slurry with water, almost the same results as the pigment can be obtained. Therefore, in the present invention, the dye that is subjected to the flushing process can also be used as a toner component. It is. The appropriate ratio of dye and pigment to resin during flushing is 10 to 60 parts by weight of dye and pigment to 100 parts by weight of resin. In addition, flushing treatment uses humic acid,
It is particularly advantageous to carry out in the presence of humates (Na salts, NH4 salts, etc.) or humic acid derivatives. The appropriate amount of these humic acids to be added is about 0.1 to 30% by weight of the dye and pigment aqueous solution.
フラッシングするのに用いられる樹脂としては、従来か
ら湿式トナー用結着樹脂とされてきたものがいずれも適
用しつるが、特に、本発明では、これにエルカ酸アミド
化合物を加えてフラッシング法により製造されたものが
好適である。この場合、エルカ酸アミド化合物の使用量
は、最終的に液体現像剤が調整された際、その液体現像
剤100重量部に対して0.01−10重量部の範囲で
あることはいうまでもない。As the resin used for flushing, any of the binder resins conventionally used as binder resins for wet toners can be used, but in particular, in the present invention, an erucic acid amide compound is added to this resin and the resin is manufactured by the flushing method. It is preferable that the In this case, it goes without saying that the amount of the erucic acid amide compound used is in the range of 0.01-10 parts by weight per 100 parts by weight of the liquid developer when the liquid developer is finally prepared. do not have.
このフラッシング処理された着色剤の製造例を幾つかあ
げれば次のとおりである。Some examples of the production of colorants subjected to flushing treatment are as follows.
着色剤製造例−l
ガロンニーダに水200g、フミン酸アンモニウム塩2
0gをよく溶解した中にカーボン(三菱#44)250
gを入れ、ニーダ−中でよく混合分散した。次に、エボ
レンE−15(コダック社製)750g及びエルカ酸ア
ミド500gを入れ、約100℃に加温混合し、水を分
離した。Colorant production example-l 200g of water and 2 humic acid ammonium salts in a gallon kneader
Carbon (Mitsubishi #44) 250 in 0g well dissolved
g was added and thoroughly mixed and dispersed in a kneader. Next, 750 g of Evolen E-15 (manufactured by Kodak) and 500 g of erucic acid amide were added and mixed while heating to about 100° C. to separate water.
更に約12o℃で4時間混線後、真空乾燥し、冷却、粉
砕してフラッシング着色剤を得た。After further mixing at about 12° C. for 4 hours, the mixture was vacuum dried, cooled, and pulverized to obtain a flushing colorant.
着色剤製造例−2
ガロンニーダに水200g、フミン酸ナトリウム塩lo
gをよく溶解した中にカーボン(モーガルΔ、コロンビ
アカーボン社製)2.50gをいれ、ニーダ−中でよく
混合分散した。次に、サンワックス+5IP600g及
びエルカ酸アミド100gを入れ、約150℃に加温混
練した。更に120℃で2時間混練後、真空乾燥し、冷
却、粉砕してフラッシング着色剤を製造した。Colorant production example-2 200g of water, sodium humate salt lo in a gallon kneader
2.50 g of carbon (Mogal Δ, manufactured by Columbia Carbon Co., Ltd.) was added to the well-dissolved solution, and the mixture was thoroughly mixed and dispersed in a kneader. Next, 600 g of Sunwax +5IP and 100 g of erucic acid amide were added and kneaded while heating to about 150°C. After further kneading at 120° C. for 2 hours, the mixture was vacuum dried, cooled, and pulverized to produce a flushing colorant.
n:I配着色剤製造例−1の手順に従って以下着色剤製
造例−3〜10のフラッシング着色剤を製造した。Flushing colorants of Colorant Production Examples 3 to 10 below were produced according to the procedure of n:I Coloring Agent Production Example-1.
着色剤製造例−3
プリンテックス■300重量部
I) E D521 500エルカ酸アミ
ド 80〃
フミン酸アンモニウム 25
水 150 〃着色剤製
造例−4
プリンテックスv300重呈部
サンワックス250P 300エルカ酸アミド
too nフミン酸アンモニウム
水
着色剤製造例−5
リーガル400
みつろう
エルカ酸アミド
フミン酸アンモニウム
水
着色剤製造例−6
リーガル400
パラフィンワックス(64℃)
エルカ酸アミド
フミン酸
水
着色剤製造例−7
フタロシアニンブルー
ロジン変性マレイン酸樹脂
エルカ酸アミド
フミン酸
水
5
50
300重量部
500〃
500〃
25〃
50
300重量部
400〃
0
0
250〃
250重量部
400 〃
100 〃
50 〃
00
着色剤製造例−8
フタロシアニングリーン
サンワックス171P
エルカ酸アミド
フミン酸
水
着色剤製造例−9
チオインジゴイド
環化ゴム
エルカ酸アミド
水
着色剤製造例−1O
プリンテックスG
アルカリブルー
アクリル樹脂
エルカ酸アミド
フミン酸カルシウム
水
250重量部
280 〃
300 N
50 〃
100 7
300重量部
300 〃
100 #
100 #
250重量部
0
800〃
100〃
5 〃
100〃
本発明に使用することが好ましい分散用樹脂としては
一般式
%式%
(R,はHまたはC113を、nは6〜20の整数を表
わす、)
であられされるビニルモノマ−Aと
一般式
%式%
)
で表わされるビニルモノマー及びビニルピリジン、ビニ
ルとロリドン、エチレングリコールジメタクリレート、
スチレン、ジビニルベンゼン、ビニルトルエンより選ば
れるモノマーBの各一種づつもしくは、数種の共重合体
、グラフト共重合体があげられる。Coloring agent production example-3 Printex ■ 300 parts by weight I) E D521 500 erucic acid amide 80 Ammonium humate 25 Water 150 Coloring agent production example-4 Printex v300 superimposed part Sunwax 250P 300 erucic acid amide too n Production example of ammonium humate water colorant-5 Regal 400 Beeswax erucic acid amide humic acid water colorant production example-6 Regal 400 Paraffin wax (64°C) Production example of erucic acid amide humic acid water colorant-7 Phthalocyanine blue rosin modified maleic acid Resin erucic acid amide humic acid water 5 50 300 parts by weight 500 500 25 50 300 parts by weight 400 0 0 250 250 parts by weight 400 100 50 00 Colorant production example-8 Phthalocyanine green sun wax 171P Erucic acid Amidohumic acid water coloring agent production example-9 Thioindigoid cyclized rubber erucic acid amide water coloring agent manufacturing example-1O Printex G Alkaline blue acrylic resin Calcium erucamide humic acid water 250 parts by weight 280 〃 300 N 50 〃 100 7 300 parts by weight 300 〃 100 # 100 # 250 parts by weight 0 800 100 5 100 The dispersing resin preferably used in the present invention has the general formula % (R, represents H or C113, and n represents 6 to 20). (representing an integer) Vinyl monomer A represented by the general formula %) and vinyl pyridine, vinyl and lolidone, ethylene glycol dimethacrylate,
Examples include copolymers and graft copolymers of each type of monomer B selected from styrene, divinylbenzene, and vinyltoluene, or several types of monomers.
またシリコーン溶剤を担持液として含むときには、分散
性を上げるためにアクロイル基を有するシリコン材料、
信越シリコン社製のL S 4080などを共重合させ
ても良いし、同様に東亜合成化学社製のAK−5、チッ
ソ社製のTMO701,1”M0711、FMO721
、FMO725を使用しても良い。In addition, when a silicone solvent is included as a supporting liquid, a silicone material having an acroyl group is used to improve dispersibility.
L S 4080 manufactured by Shin-Etsu Silicon Co., Ltd., etc. may be copolymerized, and similarly, AK-5 manufactured by Toagosei Chemical Co., Ltd., TMO701, 1"M0711, FMO721 manufactured by Chisso Corporation, etc. may be copolymerized.
, FMO725 may also be used.
これらの着色材、樹脂、担体液をボールミル、キティー
ミル、ディスクミル、ビンミルなどの分散機に投入、分
散、混練を行い濃縮トナーを調製し、これを本発明の担
持液中に分散させることにより現像液を得ることができ
る。By putting these coloring materials, resins, and carrier liquid into a dispersing machine such as a ball mill, kitty mill, disk mill, bottle mill, etc., dispersing and kneading them to prepare a concentrated toner, and dispersing this in the carrier liquid of the present invention. A developer can be obtained.
(実施例1 以下の実施例中「部」は全て「重喰部」を表わす。(Example 1 In the following examples, all "parts" represent "heavy parts".
実施例1
着色剤(tA造例=1) 50部メタ
アクリレート(80/101515)共重合体のアイソ
パー820%溶液 too部アイソパー
H(EXXSON社商品名) 2001をボー
ルミルに入れて24時間分散後、さらにアイソパーHを
300部加え、1時間分散し、これを濃縮トナーとした
。これを200 g取り、FC−72(住人3M社製)
50%とKPO3(信越シリコン社製、粘度3cst)
50%との混合溶媒lQ中に希釈し、現像剤とした。Example 1 Colorant (tA formulation example = 1) 50 parts Isopar 820% solution of methacrylate (80/101515) copolymer Too part Isopar H (trade name of EXXSON) 2001 was placed in a ball mill and dispersed for 24 hours, and then Furthermore, 300 parts of Isopar H was added and dispersed for 1 hour to obtain a concentrated toner. Take 200 g of this and add FC-72 (manufactured by 3M)
50% and KPO3 (manufactured by Shin-Etsu Silicon Co., Ltd., viscosity 3cst)
It was diluted in a mixed solvent 1Q with 50% and used as a developer.
実施例2
着色剤(製造例−2) 60部アイソ
バート1
100部
これを実施例1と同様にして現像剤を得た。Example 2 Colorant (Production Example-2) 60 parts Isovert 1 100 parts A developer was obtained in the same manner as in Example 1.
実施例3
着色剤として、製造例−3のものに代えた他は実施例1
と同様にして現像剤を調製した。Example 3 Same as Example 1 except that the coloring agent was replaced with that of Production Example-3.
A developer was prepared in the same manner as above.
実施例4
スペシャルブラック−4300
部ラウリルメタクリレートルアクリル
(85/+5)共重合体 80部ア
イソパーL、 200部エ
ルカ酸アミド 5o部をアトラ
イターに入れて24時間分散後、さらにアイソパー1(
を300部加え、1時間分散し、これを濃縮トナーとし
、実施例1と同様にした現像剤を調製した。Example 4 Special Black - 4300 parts lauryl methacrylate toluacrylic (85/+5) copolymer 80 parts Isopar L, 200 parts erucic acid amide 50 parts were placed in an attritor, dispersed for 24 hours, and then further mixed with Isopar 1 (
A developer was prepared in the same manner as in Example 1 by adding 300 parts of the mixture and dispersing it for 1 hour to obtain a concentrated toner.
比較例
実施例1〜3において希釈剤をアイソパーHとした以外
は同様にして、それぞれ比較現像剤l〜3を得た。Comparative Example Comparative developers 1 to 3 were obtained in the same manner as in Examples 1 to 3 except that Isopar H was used as the diluent.
リコー!81 C75085の定着部を熱ロール定着に
改良した試験機でオイルレスで定着試験を行った。その
結果は次表の通りであった。Ricoh! An oil-less fixing test was conducted using a testing machine in which the fixing section of 81 C75085 was improved to a hot roll fixer. The results are shown in the table below.
以上の結果より明らかなとおり、本発明現像剤によりオ
フセット現象を示さない熱ローラ定着可能な範囲の温度
中が得られ、熱ローラ定着が可能であることがわかる。As is clear from the above results, it can be seen that the developer of the present invention provides a temperature within the range in which heat roller fixation is possible without an offset phenomenon, and that heat roller fixation is possible.
また密閉された室内で、試験複写機を用い連続コピーを
行い、溶剤ガス濃度を測定したところ、比較現像剤を用
いた場合はいずれも300〜360pp+eに対し1本
発明現像剤ではいずれも80〜150ppmと半減して
いた。Continuous copying was carried out using a test copying machine in a closed room, and the solvent gas concentration was measured. When the comparison developer was used, the concentration of solvent gas was 300 to 360 pp+e, whereas when the developer of the present invention was used, it was 80 to The concentration had been halved to 150 ppm.
(効果1
本発明現像剤を用いることによ番ハ定着ロールにオイル
塗布を行わなくても、オフセット現象を起こすことなく
、熱ロール定着が可能となり、コンパクトな複写機で高
速、かつ低エネルギ一定着が可能となった。また、複写
機より発生する炭化水素系ガス量も低減した。(Effect 1) By using the developer of the present invention, it is possible to perform hot roll fixing without causing an offset phenomenon without applying oil to the fixing roll, and it is possible to use a compact copying machine at high speed and with constant low energy. The amount of hydrocarbon gas generated by copying machines has also been reduced.
Claims (1)
たはシリコン系溶剤との混合液体からなる高抵抗低誘電
率の担体液中に、着色剤と樹脂とからなるトナー粒子を
分散してなる静電写真用液体現像剤において、エルカ酸
アミド化合物を添加含有せしめてなることを特徴とする
静電荷像用液体現像剤。(1) Toner particles made of a colorant and resin are dispersed in a carrier liquid of high resistance and low dielectric constant made of a mixed liquid of a fluorine-based solvent, an aliphatic hydrocarbon solvent, and/or a silicone-based solvent. A liquid developer for electrostatic images, characterized in that the liquid developer for electrostatic images contains an erucic acid amide compound.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP1342245A JP2826872B2 (en) | 1989-12-28 | 1989-12-28 | Liquid developer for electrostatic image |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP1342245A JP2826872B2 (en) | 1989-12-28 | 1989-12-28 | Liquid developer for electrostatic image |
Publications (2)
Publication Number | Publication Date |
---|---|
JPH03200266A true JPH03200266A (en) | 1991-09-02 |
JP2826872B2 JP2826872B2 (en) | 1998-11-18 |
Family
ID=18352232
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP1342245A Expired - Fee Related JP2826872B2 (en) | 1989-12-28 | 1989-12-28 | Liquid developer for electrostatic image |
Country Status (1)
Country | Link |
---|---|
JP (1) | JP2826872B2 (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2014174258A (en) * | 2013-03-07 | 2014-09-22 | Fuji Xerox Co Ltd | Liquid developer, developer cartridge, process cartridge, image forming apparatus, and image forming method |
-
1989
- 1989-12-28 JP JP1342245A patent/JP2826872B2/en not_active Expired - Fee Related
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2014174258A (en) * | 2013-03-07 | 2014-09-22 | Fuji Xerox Co Ltd | Liquid developer, developer cartridge, process cartridge, image forming apparatus, and image forming method |
Also Published As
Publication number | Publication date |
---|---|
JP2826872B2 (en) | 1998-11-18 |
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