JPH03200263A - Liquid developer for electrostatic charge image - Google Patents
Liquid developer for electrostatic charge imageInfo
- Publication number
- JPH03200263A JPH03200263A JP1342242A JP34224289A JPH03200263A JP H03200263 A JPH03200263 A JP H03200263A JP 1342242 A JP1342242 A JP 1342242A JP 34224289 A JP34224289 A JP 34224289A JP H03200263 A JPH03200263 A JP H03200263A
- Authority
- JP
- Japan
- Prior art keywords
- erucic acid
- acid amide
- liquid developer
- added
- compd
- 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 28
- 239000011347 resin Substances 0.000 claims abstract description 27
- 229920005989 resin Polymers 0.000 claims abstract description 27
- -1 erucic acid amine Chemical class 0.000 claims abstract description 23
- 239000003086 colorant Substances 0.000 claims abstract description 22
- 239000002904 solvent Substances 0.000 claims abstract description 16
- 229920001296 polysiloxane Polymers 0.000 claims abstract description 8
- 239000002245 particle Substances 0.000 claims abstract description 5
- 239000000654 additive Substances 0.000 claims 1
- 230000000996 additive effect Effects 0.000 claims 1
- 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 6
- 150000002430 hydrocarbons Chemical class 0.000 abstract description 6
- 239000004215 Carbon black (E152) Substances 0.000 abstract description 5
- 239000011230 binding agent Substances 0.000 abstract description 4
- 239000003795 chemical substances by application Substances 0.000 abstract description 4
- 229910052751 metal Inorganic materials 0.000 abstract description 2
- 239000002184 metal Substances 0.000 abstract description 2
- DPUOLQHDNGRHBS-UHFFFAOYSA-N Brassidinsaeure Natural products CCCCCCCCC=CCCCCCCCCCCCC(O)=O DPUOLQHDNGRHBS-UHFFFAOYSA-N 0.000 abstract 1
- URXZXNYJPAJJOQ-UHFFFAOYSA-N Erucic acid Natural products CCCCCCC=CCCCCCCCCCCCC(O)=O URXZXNYJPAJJOQ-UHFFFAOYSA-N 0.000 abstract 1
- 230000000903 blocking effect Effects 0.000 abstract 1
- 230000003247 decreasing effect Effects 0.000 abstract 1
- 239000002612 dispersion medium Substances 0.000 abstract 1
- 238000004519 manufacturing process Methods 0.000 description 17
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 13
- 239000000049 pigment Substances 0.000 description 13
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 13
- 238000011010 flushing procedure Methods 0.000 description 12
- 238000000034 method Methods 0.000 description 9
- 239000004698 Polyethylene Substances 0.000 description 8
- 229920000573 polyethylene Polymers 0.000 description 8
- 239000007789 gas Substances 0.000 description 7
- 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
- 239000000463 material Substances 0.000 description 4
- 239000000203 mixture Substances 0.000 description 4
- 239000003921 oil Substances 0.000 description 4
- 239000012188 paraffin wax Substances 0.000 description 4
- 239000010703 silicon Substances 0.000 description 4
- CNPVJWYWYZMPDS-UHFFFAOYSA-N 2-methyldecane Chemical compound CCCCCCCCC(C)C CNPVJWYWYZMPDS-UHFFFAOYSA-N 0.000 description 3
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical class N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 3
- 150000001338 aliphatic hydrocarbons Chemical class 0.000 description 3
- 230000000052 comparative effect Effects 0.000 description 3
- 238000010438 heat treatment Methods 0.000 description 3
- 239000000178 monomer Substances 0.000 description 3
- 150000003839 salts Chemical class 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
- UAUDZVJPLUQNMU-UHFFFAOYSA-N Erucasaeureamid Natural products CCCCCCCCC=CCCCCCCCCCCCC(N)=O UAUDZVJPLUQNMU-UHFFFAOYSA-N 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
- 229920001577 copolymer Polymers 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
- 239000006185 dispersion Substances 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 238000004898 kneading Methods 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
- 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
- 229920002545 silicone oil Polymers 0.000 description 2
- 239000011734 sodium Substances 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- BIIBYWQGRFWQKM-JVVROLKMSA-N (2S)-N-[4-(cyclopropylamino)-3,4-dioxo-1-[(3S)-2-oxopyrrolidin-3-yl]butan-2-yl]-2-[[(E)-3-(2,4-dichlorophenyl)prop-2-enoyl]amino]-4,4-dimethylpentanamide Chemical compound CC(C)(C)C[C@@H](C(NC(C[C@H](CCN1)C1=O)C(C(NC1CC1)=O)=O)=O)NC(/C=C/C(C=CC(Cl)=C1)=C1Cl)=O BIIBYWQGRFWQKM-JVVROLKMSA-N 0.000 description 1
- 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
- FFRBMBIXVSCUFS-UHFFFAOYSA-N 2,4-dinitro-1-naphthol Chemical compound C1=CC=C2C(O)=C([N+]([O-])=O)C=C([N+]([O-])=O)C2=C1 FFRBMBIXVSCUFS-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
- HFGHRUCCKVYFKL-UHFFFAOYSA-N 4-ethoxy-2-piperazin-1-yl-7-pyridin-4-yl-5h-pyrimido[5,4-b]indole Chemical compound C1=C2NC=3C(OCC)=NC(N4CCNCC4)=NC=3C2=CC=C1C1=CC=NC=C1 HFGHRUCCKVYFKL-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-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 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
- 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
- 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
- 241000692870 Inachis io Species 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
- WHNWPMSKXPGLAX-UHFFFAOYSA-N N-Vinyl-2-pyrrolidone Chemical compound C=CN1CCCC1=O WHNWPMSKXPGLAX-UHFFFAOYSA-N 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
- 229920006243 acrylic copolymer Polymers 0.000 description 1
- AOADSHDCARXSGL-ZMIIQOOPSA-M alkali blue 4B Chemical compound CC1=CC(/C(\C(C=C2)=CC=C2NC2=CC=CC=C2S([O-])(=O)=O)=C(\C=C2)/C=C/C\2=N\C2=CC=CC=C2)=CC=C1N.[Na+] AOADSHDCARXSGL-ZMIIQOOPSA-M 0.000 description 1
- 239000008346 aqueous phase Substances 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- HEQCHSSPWMWXBH-UHFFFAOYSA-L barium(2+) 1-[(2-carboxyphenyl)diazenyl]naphthalen-2-olate Chemical compound [Ba++].Oc1ccc2ccccc2c1N=Nc1ccccc1C([O-])=O.Oc1ccc2ccccc2c1N=Nc1ccccc1C([O-])=O HEQCHSSPWMWXBH-UHFFFAOYSA-L 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
- 239000004020 conductor Substances 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
- 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
- STVZJERGLQHEKB-UHFFFAOYSA-N ethylene glycol dimethacrylate Substances CC(=C)C(=O)OCCOC(=O)C(C)=C STVZJERGLQHEKB-UHFFFAOYSA-N 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
- 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
- 125000002496 methyl group Chemical group [H]C([H])([H])* 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
- 239000000025 natural resin Substances 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
- 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
- XULSCZPZVQIMFM-IPZQJPLYSA-N odevixibat Chemical compound C12=CC(SC)=C(OCC(=O)N[C@@H](C(=O)N[C@@H](CC)C(O)=O)C=3C=CC(O)=CC=3)C=C2S(=O)(=O)NC(CCCC)(CCCC)CN1C1=CC=CC=C1 XULSCZPZVQIMFM-IPZQJPLYSA-N 0.000 description 1
- 239000012860 organic pigment Substances 0.000 description 1
- 235000012736 patent blue V Nutrition 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
- 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
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
- 229920002554 vinyl polymer Polymers 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
- 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1
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 1) 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 heat roll fixing roll, JP-A-63
-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 is to reduce hydrocarbon-based solvent gases generated from copying machines.
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1
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。担体液に
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
シリコーン系溶剤を用い、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”を防止する点にある。Arrangement 1 of the Invention In recent years, hot roll fixing has been proposed as a method of fixing a liquid developer with high thermal efficiency and capable of high-speed fixing. If a hydrocarbon solvent is used as the carrier liquid and this fixing method is adopted,
Compared to conventional atmospheric fixing, the amount of solvent gas emitted per unit number of sheets is slightly reduced, but a large amount of solvent gas is generated when a large number of sheets are copied at high speed. Also,
It was necessary to apply silicone oil to improve the releasability between the toner layer and the fixing roll. The present invention uses a silicone solvent as a carrier liquid to improve the above-mentioned drawbacks, increase the cohesive force of the toner, and prevent so-called "hot offset".
本発明に使用されるシリコーン系の溶剤としては、KF
96 (信越シリコン)、5H200,5H344(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、ソルツベツソ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3
Cst以下がよい。The silicone solvent used in the present invention includes KF
96 (Shin-Etsu Silicon), 5H200, 5H344 (Toshi Silicon), TSF451 (Toshiba Silicon), etc. In addition, decamethyltetrasiloxane, octamethyltrisiloxane, etc. may 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. In addition to Isopar E, G, H, and L, there are V, Shell Sol 71 manufactured by Shell Oil Co., and Salt Betsu So 150, etc.), and these may be used by appropriately mixing them. To reduce the transfer agent, the carrier liquid should be less than 1 ocst, preferably 3 ocst.
Cst or less is preferable.
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
.0l−10fi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 0l-10fi parts, preferably 0.1-5 parts by weight.
電子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(担体液)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す、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 liquid), causing it to peel off against the metal heat fixing roller. The agent acts as an anti-blocking property, so that toner is less likely to adhere to the fuser 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)、ラーベン
1035、シーベン1252.ニユースペクトn (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L(以上キャボット社製)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Y1ナフト
ールイエロー81ナフトールレッド、リソ−シフアース
トイエロー2G、パーマネントレツド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、レーキ
レッドD、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 Kasei Corporation), Raven 1035, Sieben 1252. New Spect N (manufactured by Columbia Carbon), Regal 400.660
, Black Var 900, 1100, 1300, Mogul L (manufactured by Cabot) and other inorganic pigments, and phthalocyanine blue, phthalocyanine green, sky blue, rhodamine lake, malachite green lake,
Methyl violet lake, peacock blue lake,
Naphthol Green B, Naphthol Green Y1 Naphthol Yellow 81 Naphthol Red, Litho-Siferst Yellow 2G, Permanent Red 4R, Brilliant First Scarlet, Hansa Yellow, Benzidine Yellow, Lysole Red, Lake Red C, Lake Red D, Brilliant Carmine 6B, Examples include organic pigments such as Permanent Red F5R, Pigment Scarlet 3B Indigo, 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、オレフィン−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 polyolefin, acrylic resin, rosin-modified resin, styrene-butadiene resin, natural resin, olefin-acrylic copolymer, paraffin wax, and the like. 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
アライド
ケミカル
コダック
工注化成
純正薬品
ヘキスト
銘柄
ACポリエチレン 1702
ACポリエチレン617,617A
八Cポリエチレン 9,9A
ACポリエチレン 430
ACポリエチレン 405
ACポリエチレン 401
ACポリエチレン 540
ACポリエチレン 580
エボレン N−14
エポレン 1シー15
サンワックス +31−P
サンワックス 151=P
サンワックス +61−P
サンワックス 165−P
サンワックス +71−P
サンワックス E−250r’
サンワックス E−300P
パラフィンワックス
PED 521
PED 543 110PED
153 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 Allied Chemical Kodak Kosei Chemicals Genuine Hoechst Brand AC Polyethylene 1702 AC Polyethylene 617,617A 8C Polyethylene 9,9A AC Polyethylene 430 AC Polyethylene 405 AC Polyethylene 401 AC Polyethylene 540 AC Polyethylene 580 Evolen N-14 Epolene 1 Sea 15 Sunwax +31-P Sunwax 151=P Sunwax +61-P Sunwax 165-P Sunwax +71-P Sunwax E-250r' Sunwax E-300P Paraffin wax PED 521 PED 543 110PED
153 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)又はフミン酸銹導
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 crushed. be. In the present invention, this material is referred to as "flushing pigment".
I will call it . Note that it is also possible to take measures such as removing 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 undergoes 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 salt conductors. 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 to 10 parts by weight based on 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−1
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-1 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120℃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 120° C. for 4 hours, the mixture was vacuum dried, cooled, and crushed 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A、コロンビ
アカーボン社製)250gをいれ、ニーダ−中でよく混
合分散した。次に、サンワックス151P600g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時間混線後、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
250 g of carbon (Mogul A, 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 151P and 100 g of erucic acid amide were added and kneaded while heating to about 150°C. After further mixing at 120° C. for 2 hours, the mixture was vacuum dried, cooled, and pulverized to produce a flushing colorant.
前記着色剤製造例−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 Colorant Production Example 1.
着色剤製造例−3
プリンテックスV
P E 0521
300fft量部
500 〃
80 〃
25 〃
150 〃
エルカ酸アミド
フミン酸アンモニウム
水
着色剤製造例−4
プリンテックスV
サンワックス250P
エルカ酸アミド
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
300重量部
00
100 n
5
150 〃
300ff!量部
00
500 〃
25 〃
250 〃
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
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
300重量部
00
0 tt
5Q //
50
250重量部
00
00
5Q tt
100 〃
250重量部
80
00
50 〃
100 /7
300重量部
環化ゴム
エルカ酸アミド
水
着色剤製造例−10
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
00
100 〃
too lI
250重量部
50 〃
800 〃
100 〃
5 〃
100 II
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%
nは6〜20の整数を表
わす。)
であられされるビニルモノマー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
ルピロリドン、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 V P E 0521 300 fft parts 500 〃 80 〃 25〃 150 〃 Erucic acid amide humate ammonium water coloring agent manufacturing example-4 Printex V Sunwax 250P Erucic acid amide humic acid ammonium water coloring agent production Example-5 Regal 400 Beeswax ammonium erucate humate water 300 parts by weight 00 100 n 5 150 〃 300ff! Parts 00 500 〃 25 〃 250 〃 Coloring agent production example-6 Regal 400 Paraffin wax (64°C) Erucic acid amide humic acid water coloring agent production example-7 Phthalocyanine blue rosin modified maleic acid resin Erucic acid amide humic acid water coloring agent manufacturing example -8 Phthalocyanine green sunwax 171P Erucic acid amide humic acid water colorant production example -9 Thioindigoid 300 parts by weight 00 0 tt 5Q // 50 250 parts by weight 00 00 5Q tt 100 〃 250 parts by weight 80 00 50 〃 100 /7 300 parts by weight Partially cyclized rubber erucamide water coloring agent production example-10 Printex G Alkali blue acrylic resin erucamide calcium humate water 00 100 Too lI 250 parts by weight 50 800 100 5 100 II Use in the present invention A preferred dispersing resin is the general formula %, where n represents an integer from 6 to 20. ) Vinyl monomer A represented by the general formula %) and vinyl pyridine, vinyl pyrrolidone, 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.
またシリコン溶剤への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LS40
80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、FM07
11、FMO721、FMO725を使用しても良い。In addition, in order to improve dispersibility in silicone solvents, silicone material with an acroyl group, LS40 manufactured by Shin-Etsu Silicon Co., Ltd.
Similarly, AK-5 manufactured by Toagosei Kagaku Co., Ltd., TMO701 manufactured by Chisso Co., Ltd., and FM07 may be copolymerized.
11, FMO721 and FMO725 may be used.
これらの着色材、樹脂、担体液をボールミル、キテイー
ミル、ディスクミル、ビンミルなどの分散機に投入、分
散、混線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。These coloring materials, resins, and carrier liquids are put into a dispersing machine such as a ball mill, kitty mill, disk mill, and bottle mill, and then dispersed and mixed to prepare a concentrated toner, which is then dispersed in the carrier liquid of the present invention for development. liquid can be obtained.
(実施例1 以下の実施例中[部」は全て「重量部」を表わす。(Example 1 In the following examples, all "parts" represent "parts by weight."
実施例1
着色剤(製造例−1) 50部アイソ
パー820%溶液 100部アイソパー
H(EXXSON社商品名)200部をボールミルに入
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2
00g取り、KPO3(信越シリコン製、粘度3cst
)IQ中に希釈し、現像剤とした。Example 1 Colorant (Production Example-1) 50 parts Isopar 820% solution 100 parts 200 parts Isopar H (trade name of EXXSON) was placed in a ball mill and dispersed for 24 hours, then 300 parts of Isopar H was added and dispersed for 1 hour. This was used as a concentrated toner. This 2
00g taken, KPO3 (manufactured by Shin-Etsu Silicone, viscosity 3cst)
) It was diluted in IQ and used as a developer.
実施例2
着色剤(製造例−2) 60部ステア
リルメタクリレート/メチルメタアイソバート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 Stearyl methacrylate/methyl metaisobate 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
(85/15)共重合体 80部ア
イソパーL200部
エルカ酸アミド 50部をア
トライターに入れて24時間分散後、さらにアイソバー
トI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200g取り、KPO3(信越シリコン
製、粘度3cst)IQ中に希釈し、現像剤とした。Example 4 Special Black - 4300 parts lauryl methacrylate toluacrylic (85/15) copolymer 80 parts Isopar L 200 parts Erucic acid amide 50 parts were placed in an attritor and dispersed for 24 hours, then 300 parts of Isovert I was added and 1 After time dispersion, this was made into a concentrated toner. 200 g of this was taken and diluted in KPO3 (manufactured by Shin-Etsu Silicon, viscosity 3 cst) IQ to prepare a developer.
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1〜3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!ICT5085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 with the fixing section of ICT5085 improved to a hot roll fixer. The results are shown in the table below.
であることがわかる。It can be seen that it is.
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300〜360ppmに対し、本発
明現像剤ではいずれも80〜150ppmと半減してい
た。Continuous copying was performed using a test copying machine in a closed room, and the solvent gas concentration was measured. When using the comparative developer, the concentration of solvent gas was 300 to 360 ppm, whereas with the developer of the present invention, it was 80 to 360 ppm. 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り、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 applying oil to the fixing roll and without causing an offset phenomenon, allowing a compact copying machine to achieve high speed and constant fixation with low energy. The amount of hydrocarbon gas generated by copying machines has also been reduced.
Claims (1)
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) In an electrostatographic liquid developer in which toner particles made of a colorant and resin are dispersed in a high-resistance, low-permittivity carrier liquid containing a silicone solvent as a main component, an erucic acid amide compound is used. A liquid developer for electrostatic images characterized by containing an additive.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP1342242A JP2826870B2 (en) | 1989-12-28 | 1989-12-28 | Liquid developer for electrostatic image |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP1342242A JP2826870B2 (en) | 1989-12-28 | 1989-12-28 | Liquid developer for electrostatic image |
Publications (2)
Publication Number | Publication Date |
---|---|
JPH03200263A true JPH03200263A (en) | 1991-09-02 |
JP2826870B2 JP2826870B2 (en) | 1998-11-18 |
Family
ID=18352210
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP1342242A Expired - Fee Related JP2826870B2 (en) | 1989-12-28 | 1989-12-28 | Liquid developer for electrostatic image |
Country Status (1)
Country | Link |
---|---|
JP (1) | JP2826870B2 (en) |
-
1989
- 1989-12-28 JP JP1342242A patent/JP2826870B2/en not_active Expired - Fee Related
Also Published As
Publication number | Publication date |
---|---|
JP2826870B2 (en) | 1998-11-18 |
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