JPH0582941B2 - - Google Patents
Info
- Publication number
- JPH0582941B2 JPH0582941B2 JP60218600A JP21860085A JPH0582941B2 JP H0582941 B2 JPH0582941 B2 JP H0582941B2 JP 60218600 A JP60218600 A JP 60218600A JP 21860085 A JP21860085 A JP 21860085A JP H0582941 B2 JPH0582941 B2 JP H0582941B2
- Authority
- JP
- Japan
- Prior art keywords
- resin
- formula
- present
- chemical formula
- 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.)
- Expired - Lifetime
Links
- 239000007788 liquid Substances 0.000 claims description 28
- 229920005989 resin Polymers 0.000 claims description 27
- 239000011347 resin Substances 0.000 claims description 27
- 229920001577 copolymer Polymers 0.000 claims description 13
- 239000000178 monomer Substances 0.000 claims description 11
- IWTYTFSSTWXZFU-UHFFFAOYSA-N 3-chloroprop-1-enylbenzene Chemical compound ClCC=CC1=CC=CC=C1 IWTYTFSSTWXZFU-UHFFFAOYSA-N 0.000 claims description 8
- 239000000126 substance Substances 0.000 claims description 5
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 4
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims description 2
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims description 2
- 125000000217 alkyl group Chemical group 0.000 claims description 2
- 125000003710 aryl alkyl group Chemical group 0.000 claims description 2
- 125000003118 aryl group Chemical group 0.000 claims description 2
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 2
- 229910052799 carbon Inorganic materials 0.000 claims description 2
- 125000004432 carbon atom Chemical group C* 0.000 claims description 2
- 239000000470 constituent Substances 0.000 claims description 2
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 2
- 125000004433 nitrogen atom Chemical group N* 0.000 claims description 2
- 229910052760 oxygen Inorganic materials 0.000 claims description 2
- 239000001301 oxygen Substances 0.000 claims description 2
- 239000011593 sulfur Substances 0.000 claims description 2
- 229910052717 sulfur Inorganic materials 0.000 claims description 2
- 229920000642 polymer Polymers 0.000 description 26
- 239000002245 particle Substances 0.000 description 14
- -1 N,N-dimethylamino-methoxymethylstyrene Chemical compound 0.000 description 13
- 239000003086 colorant Substances 0.000 description 13
- 230000015572 biosynthetic process Effects 0.000 description 10
- 238000000034 method Methods 0.000 description 10
- 238000003786 synthesis reaction Methods 0.000 description 10
- 229910052751 metal Inorganic materials 0.000 description 7
- 239000002184 metal Substances 0.000 description 7
- 150000003839 salts Chemical class 0.000 description 7
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 6
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 6
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 6
- 150000001875 compounds Chemical class 0.000 description 6
- 239000002904 solvent Substances 0.000 description 6
- CNPVJWYWYZMPDS-UHFFFAOYSA-N 2-methyldecane Chemical compound CCCCCCCCC(C)C CNPVJWYWYZMPDS-UHFFFAOYSA-N 0.000 description 5
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 5
- 230000000052 comparative effect Effects 0.000 description 5
- 239000000203 mixture Substances 0.000 description 5
- 229920000178 Acrylic resin Polymers 0.000 description 4
- 239000004925 Acrylic resin Substances 0.000 description 4
- 239000006229 carbon black Substances 0.000 description 4
- 239000003795 chemical substances by application Substances 0.000 description 4
- 239000000975 dye Substances 0.000 description 4
- 230000000694 effects Effects 0.000 description 4
- 239000011521 glass Substances 0.000 description 4
- 229910052757 nitrogen Inorganic materials 0.000 description 4
- 108091008695 photoreceptors Proteins 0.000 description 4
- 229920003048 styrene butadiene rubber Polymers 0.000 description 4
- RSWGJHLUYNHPMX-UHFFFAOYSA-N Abietic-Saeure Natural products C12CCC(C(C)C)=CC2=CCC2C1(C)CCCC2(C)C(O)=O RSWGJHLUYNHPMX-UHFFFAOYSA-N 0.000 description 3
- 239000005062 Polybutadiene Substances 0.000 description 3
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 3
- 229920000180 alkyd Polymers 0.000 description 3
- 239000011324 bead Substances 0.000 description 3
- 239000002270 dispersing agent Substances 0.000 description 3
- 239000000025 natural resin Substances 0.000 description 3
- 239000003973 paint Substances 0.000 description 3
- 239000000049 pigment Substances 0.000 description 3
- 229920002857 polybutadiene Polymers 0.000 description 3
- 238000006116 polymerization reaction Methods 0.000 description 3
- 238000011160 research Methods 0.000 description 3
- 229920003002 synthetic resin Polymers 0.000 description 3
- 239000000057 synthetic resin Substances 0.000 description 3
- XDOFQFKRPWOURC-UHFFFAOYSA-N 16-methylheptadecanoic acid Chemical compound CC(C)CCCCCCCCCCCCCCC(O)=O XDOFQFKRPWOURC-UHFFFAOYSA-N 0.000 description 2
- OZAIFHULBGXAKX-UHFFFAOYSA-N 2-(2-cyanopropan-2-yldiazenyl)-2-methylpropanenitrile Chemical compound N#CC(C)(C)N=NC(C)(C)C#N OZAIFHULBGXAKX-UHFFFAOYSA-N 0.000 description 2
- KXGFMDJXCMQABM-UHFFFAOYSA-N 2-methoxy-6-methylphenol Chemical compound [CH]OC1=CC=CC([CH])=C1O KXGFMDJXCMQABM-UHFFFAOYSA-N 0.000 description 2
- BTXXTMOWISPQSJ-UHFFFAOYSA-N 4,4,4-trifluorobutan-2-one Chemical class CC(=O)CC(F)(F)F BTXXTMOWISPQSJ-UHFFFAOYSA-N 0.000 description 2
- 229910000967 As alloy Inorganic materials 0.000 description 2
- LSNNMFCWUKXFEE-UHFFFAOYSA-M Bisulfite Chemical compound OS([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-M 0.000 description 2
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 2
- 244000043261 Hevea brasiliensis Species 0.000 description 2
- RRHGJUQNOFWUDK-UHFFFAOYSA-N Isoprene Chemical compound CC(=C)C=C RRHGJUQNOFWUDK-UHFFFAOYSA-N 0.000 description 2
- KHPCPRHQVVSZAH-HUOMCSJISA-N Rosin Natural products O(C/C=C/c1ccccc1)[C@H]1[C@H](O)[C@@H](O)[C@@H](O)[C@@H](CO)O1 KHPCPRHQVVSZAH-HUOMCSJISA-N 0.000 description 2
- XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 description 2
- 239000002253 acid Substances 0.000 description 2
- 239000000654 additive Substances 0.000 description 2
- POULHZVOKOAJMA-UHFFFAOYSA-N dodecanoic acid Chemical compound CCCCCCCCCCCC(O)=O POULHZVOKOAJMA-UHFFFAOYSA-N 0.000 description 2
- 238000010438 heat treatment Methods 0.000 description 2
- 238000004898 kneading Methods 0.000 description 2
- 238000005259 measurement Methods 0.000 description 2
- PPMXDDJEXJDFMT-UHFFFAOYSA-N n,n-diethyl-3-phenylprop-2-en-1-amine Chemical compound CCN(CC)CC=CC1=CC=CC=C1 PPMXDDJEXJDFMT-UHFFFAOYSA-N 0.000 description 2
- 229920003052 natural elastomer Polymers 0.000 description 2
- 229920001194 natural rubber Polymers 0.000 description 2
- WXZMFSXDPGVJKK-UHFFFAOYSA-N pentaerythritol Chemical compound OCC(CO)(CO)CO WXZMFSXDPGVJKK-UHFFFAOYSA-N 0.000 description 2
- 239000003208 petroleum Substances 0.000 description 2
- 239000005011 phenolic resin Substances 0.000 description 2
- 229920001568 phenolic resin Polymers 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
- 229920003227 poly(N-vinyl carbazole) Polymers 0.000 description 2
- 150000003097 polyterpenes Chemical class 0.000 description 2
- 239000002244 precipitate Substances 0.000 description 2
- 239000000047 product Substances 0.000 description 2
- 238000010298 pulverizing process Methods 0.000 description 2
- 238000004062 sedimentation Methods 0.000 description 2
- 229920003051 synthetic elastomer Polymers 0.000 description 2
- 239000005061 synthetic 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
- WRIDQFICGBMAFQ-UHFFFAOYSA-N (E)-8-Octadecenoic acid Natural products CCCCCCCCCC=CCCCCCCC(O)=O WRIDQFICGBMAFQ-UHFFFAOYSA-N 0.000 description 1
- PAFMWEOWHZKACA-UHFFFAOYSA-N 1-(2-phenylethenyl)piperidine Chemical compound C1CCCCN1C=CC1=CC=CC=C1 PAFMWEOWHZKACA-UHFFFAOYSA-N 0.000 description 1
- ZJNARIDKWBUMOZ-UHFFFAOYSA-N 1-(3-phenylprop-2-enyl)piperidine Chemical compound C1CCCCN1CC=CC1=CC=CC=C1 ZJNARIDKWBUMOZ-UHFFFAOYSA-N 0.000 description 1
- VXHDACRESIRJOF-UHFFFAOYSA-N 1-[2-(3-phenylprop-2-enoxy)ethyl]piperidine Chemical compound C=1C=CC=CC=1C=CCOCCN1CCCCC1 VXHDACRESIRJOF-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
- IIZPXYDJLKNOIY-JXPKJXOSSA-N 1-palmitoyl-2-arachidonoyl-sn-glycero-3-phosphocholine Chemical compound CCCCCCCCCCCCCCCC(=O)OC[C@H](COP([O-])(=O)OCC[N+](C)(C)C)OC(=O)CCC\C=C/C\C=C/C\C=C/C\C=C/CCCCC IIZPXYDJLKNOIY-JXPKJXOSSA-N 0.000 description 1
- VHQGURIJMFPBKS-UHFFFAOYSA-N 2,4,7-trinitrofluoren-9-one Chemical compound [O-][N+](=O)C1=CC([N+]([O-])=O)=C2C3=CC=C([N+](=O)[O-])C=C3C(=O)C2=C1 VHQGURIJMFPBKS-UHFFFAOYSA-N 0.000 description 1
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 1
- KHOWOELMJACONO-UHFFFAOYSA-N 2-(3-phenylprop-2-enoxy)ethanamine Chemical compound NCCOCC=CC1=CC=CC=C1 KHOWOELMJACONO-UHFFFAOYSA-N 0.000 description 1
- SJIXRGNQPBQWMK-UHFFFAOYSA-N 2-(diethylamino)ethyl 2-methylprop-2-enoate Chemical compound CCN(CC)CCOC(=O)C(C)=C SJIXRGNQPBQWMK-UHFFFAOYSA-N 0.000 description 1
- JKNCOURZONDCGV-UHFFFAOYSA-N 2-(dimethylamino)ethyl 2-methylprop-2-enoate Chemical compound CN(C)CCOC(=O)C(C)=C JKNCOURZONDCGV-UHFFFAOYSA-N 0.000 description 1
- OBMRSUNAEQGDLK-UHFFFAOYSA-N 2-(dipropylamino)ethyl 2-methylprop-2-enoate Chemical compound CCCN(CCC)CCOC(=O)C(C)=C OBMRSUNAEQGDLK-UHFFFAOYSA-N 0.000 description 1
- WDQMWEYDKDCEHT-UHFFFAOYSA-N 2-ethylhexyl 2-methylprop-2-enoate Chemical compound 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
- WUPHOULIZUERAE-UHFFFAOYSA-N 3-(oxolan-2-yl)propanoic acid Chemical compound OC(=O)CCC1CCCO1 WUPHOULIZUERAE-UHFFFAOYSA-N 0.000 description 1
- CVDBTODNFIHEQA-UHFFFAOYSA-N 3-phenyl-n,n-dipropylprop-2-en-1-amine Chemical compound CCCN(CCC)CC=CC1=CC=CC=C1 CVDBTODNFIHEQA-UHFFFAOYSA-N 0.000 description 1
- XVODXZBINOXIOP-UHFFFAOYSA-N 3-phenyl-n-propylprop-2-en-1-amine Chemical compound CCCNCC=CC1=CC=CC=C1 XVODXZBINOXIOP-UHFFFAOYSA-N 0.000 description 1
- XWLLGMTXHZNRDQ-UHFFFAOYSA-N 4-(2-phenylethenyl)morpholine Chemical compound C1COCCN1C=CC1=CC=CC=C1 XWLLGMTXHZNRDQ-UHFFFAOYSA-N 0.000 description 1
- UDSHBISYNCGDRX-UHFFFAOYSA-N 4-(3-phenylprop-2-enyl)morpholine Chemical compound C1COCCN1CC=CC1=CC=CC=C1 UDSHBISYNCGDRX-UHFFFAOYSA-N 0.000 description 1
- PUMKCXCVIKEBIA-UHFFFAOYSA-N 4-[2-(3-phenylprop-2-enoxy)ethyl]morpholine Chemical compound C=1C=CC=CC=1C=CCOCCN1CCOCC1 PUMKCXCVIKEBIA-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
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 1
- 239000005639 Lauric acid Substances 0.000 description 1
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 description 1
- VMWQICMOAJXNQI-UHFFFAOYSA-N N-ethyl-N-[2-(3-phenylprop-2-enoxy)ethyl]anthracen-1-amine Chemical compound C1(=CC=CC2=CC3=CC=CC=C3C=C12)N(CC)CCOCC=CC1=CC=CC=C1 VMWQICMOAJXNQI-UHFFFAOYSA-N 0.000 description 1
- JXFKERKDYKOFTI-UHFFFAOYSA-N N-ethyl-N-[2-(3-phenylprop-2-enoxy)ethyl]phenanthren-1-amine Chemical compound C1(=CC=CC=2C3=CC=CC=C3C=CC12)N(CC)CCOCC=CC1=CC=CC=C1 JXFKERKDYKOFTI-UHFFFAOYSA-N 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
- 229910019142 PO4 Inorganic materials 0.000 description 1
- 206010034972 Photosensitivity reaction Diseases 0.000 description 1
- 239000004698 Polyethylene Substances 0.000 description 1
- BUGBHKTXTAQXES-UHFFFAOYSA-N Selenium Chemical compound [Se] BUGBHKTXTAQXES-UHFFFAOYSA-N 0.000 description 1
- 229920013623 Solprene Polymers 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
- 229910001215 Te alloy Inorganic materials 0.000 description 1
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 1
- 239000005083 Zinc sulfide Substances 0.000 description 1
- QLNFINLXAKOTJB-UHFFFAOYSA-N [As].[Se] Chemical compound [As].[Se] QLNFINLXAKOTJB-UHFFFAOYSA-N 0.000 description 1
- 238000004220 aggregation Methods 0.000 description 1
- 230000002776 aggregation Effects 0.000 description 1
- 150000001338 aliphatic hydrocarbons Chemical class 0.000 description 1
- 125000005250 alkyl acrylate group Chemical group 0.000 description 1
- 150000003973 alkyl amines Chemical class 0.000 description 1
- 150000003863 ammonium salts Chemical class 0.000 description 1
- 150000004945 aromatic hydrocarbons Chemical class 0.000 description 1
- ZCGHEBMEQXMRQL-UHFFFAOYSA-N benzyl 2-carbamoylpyrrolidine-1-carboxylate Chemical compound NC(=O)C1CCCN1C(=O)OCC1=CC=CC=C1 ZCGHEBMEQXMRQL-UHFFFAOYSA-N 0.000 description 1
- LKVJLQKCWWNRJC-UHFFFAOYSA-N buta-1,3-diene prop-2-enylbenzene Chemical compound C=CC=C.C(C1=CC=CC=C1)C=C LKVJLQKCWWNRJC-UHFFFAOYSA-N 0.000 description 1
- 229910052980 cadmium sulfide Inorganic materials 0.000 description 1
- 159000000007 calcium salts Chemical class 0.000 description 1
- 150000001735 carboxylic acids Chemical class 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- XCJYREBRNVKWGJ-UHFFFAOYSA-N copper(II) phthalocyanine Chemical compound [Cu+2].C12=CC=CC=C2C(N=C2[N-]C(C3=CC=CC=C32)=N2)=NC1=NC([C]1C=CC=CC1=1)=NC=1N=C1[C]3C=CC=CC3=C2[N-]1 XCJYREBRNVKWGJ-UHFFFAOYSA-N 0.000 description 1
- 238000011161 development Methods 0.000 description 1
- 239000003989 dielectric material Substances 0.000 description 1
- 235000014113 dietary fatty acids Nutrition 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
- DAZQAVUGEAWJSC-UHFFFAOYSA-N dodecyl 2-methylprop-2-enoate;prop-2-enoic acid Chemical compound OC(=O)C=C.CCCCCCCCCCCCOC(=O)C(C)=C DAZQAVUGEAWJSC-UHFFFAOYSA-N 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 229920001971 elastomer Polymers 0.000 description 1
- 239000003822 epoxy resin Substances 0.000 description 1
- MEGHWIAOTJPCHQ-UHFFFAOYSA-N ethenyl butanoate Chemical compound CCCC(=O)OC=C MEGHWIAOTJPCHQ-UHFFFAOYSA-N 0.000 description 1
- GLVVKKSPKXTQRB-UHFFFAOYSA-N ethenyl dodecanoate Chemical compound CCCCCCCCCCCC(=O)OC=C GLVVKKSPKXTQRB-UHFFFAOYSA-N 0.000 description 1
- 230000005496 eutectics Effects 0.000 description 1
- 229930195729 fatty acid Natural products 0.000 description 1
- 239000000194 fatty acid Substances 0.000 description 1
- 150000004665 fatty acids Chemical class 0.000 description 1
- 238000005189 flocculation Methods 0.000 description 1
- 230000016615 flocculation Effects 0.000 description 1
- 238000010528 free radical solution polymerization reaction Methods 0.000 description 1
- 238000001879 gelation Methods 0.000 description 1
- VOZRXNHHFUQHIL-UHFFFAOYSA-N glycidyl methacrylate Chemical compound CC(=C)C(=O)OCC1CO1 VOZRXNHHFUQHIL-UHFFFAOYSA-N 0.000 description 1
- 229920000578 graft copolymer Polymers 0.000 description 1
- 150000008282 halocarbons Chemical class 0.000 description 1
- 229930195733 hydrocarbon Natural products 0.000 description 1
- 150000002484 inorganic compounds Chemical class 0.000 description 1
- 229910010272 inorganic material Inorganic materials 0.000 description 1
- QXJSBBXBKPUZAA-UHFFFAOYSA-N isooleic acid Natural products CCCCCCCC=CCCCCCCCCC(O)=O QXJSBBXBKPUZAA-UHFFFAOYSA-N 0.000 description 1
- PBOSTUDLECTMNL-UHFFFAOYSA-N lauryl acrylate Chemical compound CCCCCCCCCCCCOC(=O)C=C PBOSTUDLECTMNL-UHFFFAOYSA-N 0.000 description 1
- 239000000787 lecithin Substances 0.000 description 1
- 229940067606 lecithin Drugs 0.000 description 1
- 235000010445 lecithin Nutrition 0.000 description 1
- 235000021388 linseed oil Nutrition 0.000 description 1
- 239000000944 linseed oil Substances 0.000 description 1
- 150000002689 maleic acids Chemical class 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- YPLIFKZBNCNJJN-UHFFFAOYSA-N n,n-bis(ethylamino)ethanamine Chemical compound CCNN(CC)NCC YPLIFKZBNCNJJN-UHFFFAOYSA-N 0.000 description 1
- UTZZQBFESNQSTK-UHFFFAOYSA-N n,n-diethyl-2-(3-phenylprop-2-enoxy)ethanamine Chemical compound CCN(CC)CCOCC=CC1=CC=CC=C1 UTZZQBFESNQSTK-UHFFFAOYSA-N 0.000 description 1
- DPLUMPJQXVYXBH-UHFFFAOYSA-N n,n-diethyl-2-phenylethenamine Chemical compound CCN(CC)C=CC1=CC=CC=C1 DPLUMPJQXVYXBH-UHFFFAOYSA-N 0.000 description 1
- IUDPMKQNEYFFLW-UHFFFAOYSA-N n,n-dimethyl-2-(3-phenylprop-2-enoxy)ethanamine Chemical compound CN(C)CCOCC=CC1=CC=CC=C1 IUDPMKQNEYFFLW-UHFFFAOYSA-N 0.000 description 1
- SDYRIBONPHEWCT-UHFFFAOYSA-N n,n-dimethyl-2-phenylethenamine Chemical compound CN(C)C=CC1=CC=CC=C1 SDYRIBONPHEWCT-UHFFFAOYSA-N 0.000 description 1
- SYUYXOYNRMMOGW-UHFFFAOYSA-N n,n-dimethyl-3-phenylprop-2-en-1-amine Chemical compound CN(C)CC=CC1=CC=CC=C1 SYUYXOYNRMMOGW-UHFFFAOYSA-N 0.000 description 1
- ULYMQEQTNPDBHB-UHFFFAOYSA-N n,n-dimethyl-4-(3-phenylprop-2-enoxy)butan-1-amine Chemical compound CN(C)CCCCOCC=CC1=CC=CC=C1 ULYMQEQTNPDBHB-UHFFFAOYSA-N 0.000 description 1
- UBHHTPOLMACCDD-UHFFFAOYSA-N n,n-dimethyl-4-phenylbut-3-en-1-amine Chemical compound CN(C)CCC=CC1=CC=CC=C1 UBHHTPOLMACCDD-UHFFFAOYSA-N 0.000 description 1
- XZHRQOFGAXGNET-UHFFFAOYSA-N n,n-dimethyl-6-(3-phenylprop-2-enoxy)hexan-1-amine Chemical compound CN(C)CCCCCCOCC=CC1=CC=CC=C1 XZHRQOFGAXGNET-UHFFFAOYSA-N 0.000 description 1
- GBCKRQRXNXQQPW-UHFFFAOYSA-N n,n-dimethylprop-2-en-1-amine Chemical compound CN(C)CC=C GBCKRQRXNXQQPW-UHFFFAOYSA-N 0.000 description 1
- IOIBLAONWZJMSB-UHFFFAOYSA-N n-(2-phenylethenyl)-n-propylpropan-1-amine Chemical compound CCCN(CCC)C=CC1=CC=CC=C1 IOIBLAONWZJMSB-UHFFFAOYSA-N 0.000 description 1
- XHQDITQWCPKZNE-UHFFFAOYSA-N n-(2-phenylethenyl)butan-1-amine Chemical compound CCCCNC=CC1=CC=CC=C1 XHQDITQWCPKZNE-UHFFFAOYSA-N 0.000 description 1
- DGXVARBOCWKYLN-UHFFFAOYSA-N n-(2-phenylethenyl)dodecan-1-amine Chemical compound CCCCCCCCCCCCNC=CC1=CC=CC=C1 DGXVARBOCWKYLN-UHFFFAOYSA-N 0.000 description 1
- ICNCTFBROVUZMU-UHFFFAOYSA-N n-(2-phenylethenyl)octan-1-amine Chemical compound CCCCCCCCNC=CC1=CC=CC=C1 ICNCTFBROVUZMU-UHFFFAOYSA-N 0.000 description 1
- FRAASECWAYKGFK-UHFFFAOYSA-N n-(2-phenylethenyl)propan-1-amine Chemical compound CCCNC=CC1=CC=CC=C1 FRAASECWAYKGFK-UHFFFAOYSA-N 0.000 description 1
- AZZYKBHEGUJORL-UHFFFAOYSA-N n-(3-phenylprop-2-enyl)butan-1-amine Chemical compound CCCCNCC=CC1=CC=CC=C1 AZZYKBHEGUJORL-UHFFFAOYSA-N 0.000 description 1
- AERVVKZMWTVTOJ-UHFFFAOYSA-N n-(3-phenylprop-2-enyl)dodecan-1-amine Chemical compound CCCCCCCCCCCCNCC=CC1=CC=CC=C1 AERVVKZMWTVTOJ-UHFFFAOYSA-N 0.000 description 1
- PUINGCLHDWQAHU-UHFFFAOYSA-N n-(3-phenylprop-2-enyl)octan-1-amine Chemical compound CCCCCCCCNCC=CC1=CC=CC=C1 PUINGCLHDWQAHU-UHFFFAOYSA-N 0.000 description 1
- XNEZOERGZGNRHC-UHFFFAOYSA-N n-[2-(3-phenylprop-2-enoxy)ethyl]-n-propylpropan-1-amine Chemical compound CCCN(CCC)CCOCC=CC1=CC=CC=C1 XNEZOERGZGNRHC-UHFFFAOYSA-N 0.000 description 1
- LGDKAZWSTVXTLD-UHFFFAOYSA-N n-[2-(3-phenylprop-2-enoxy)ethyl]butan-1-amine Chemical compound CCCCNCCOCC=CC1=CC=CC=C1 LGDKAZWSTVXTLD-UHFFFAOYSA-N 0.000 description 1
- VJPVWYMYGMIZSN-UHFFFAOYSA-N n-[2-(3-phenylprop-2-enoxy)ethyl]dodecan-1-amine Chemical compound CCCCCCCCCCCCNCCOCC=CC1=CC=CC=C1 VJPVWYMYGMIZSN-UHFFFAOYSA-N 0.000 description 1
- IPTKNUSOWAYGAL-UHFFFAOYSA-N n-[2-(3-phenylprop-2-enoxy)ethyl]propan-1-amine Chemical compound CCCNCCOCC=CC1=CC=CC=C1 IPTKNUSOWAYGAL-UHFFFAOYSA-N 0.000 description 1
- FZWLMRCYGIRJHR-UHFFFAOYSA-N n-benzyl-n-ethyl-2-(3-phenylprop-2-enoxy)ethanamine Chemical compound C=1C=CC=CC=1CN(CC)CCOCC=CC1=CC=CC=C1 FZWLMRCYGIRJHR-UHFFFAOYSA-N 0.000 description 1
- OARCFNQARHZCPD-UHFFFAOYSA-N n-benzyl-n-ethyl-2-phenylethenamine Chemical compound C=1C=CC=CC=1C=CN(CC)CC1=CC=CC=C1 OARCFNQARHZCPD-UHFFFAOYSA-N 0.000 description 1
- QZQCEOPYBRKLSV-UHFFFAOYSA-N n-benzyl-n-ethyl-3-phenylprop-2-en-1-amine Chemical compound C=1C=CC=CC=1CN(CC)CC=CC1=CC=CC=C1 QZQCEOPYBRKLSV-UHFFFAOYSA-N 0.000 description 1
- AYDLVCHMZVPNEM-UHFFFAOYSA-N n-benzyl-n-methyl-2-(3-phenylprop-2-enoxy)ethanamine Chemical compound C=1C=CC=CC=1CN(C)CCOCC=CC1=CC=CC=C1 AYDLVCHMZVPNEM-UHFFFAOYSA-N 0.000 description 1
- ADHFEFURXGIMRA-UHFFFAOYSA-N n-benzyl-n-methyl-2-phenylethenamine Chemical compound C=1C=CC=CC=1C=CN(C)CC1=CC=CC=C1 ADHFEFURXGIMRA-UHFFFAOYSA-N 0.000 description 1
- VCFSFBCCSGVCHZ-UHFFFAOYSA-N n-benzyl-n-methyl-3-phenylprop-2-en-1-amine Chemical compound C=1C=CC=CC=1CN(C)CC=CC1=CC=CC=C1 VCFSFBCCSGVCHZ-UHFFFAOYSA-N 0.000 description 1
- LKBJBKVZFZPKRL-UHFFFAOYSA-N n-butyl-n-(2-phenylethenyl)butan-1-amine Chemical compound CCCCN(CCCC)C=CC1=CC=CC=C1 LKBJBKVZFZPKRL-UHFFFAOYSA-N 0.000 description 1
- TTWJFBWTJAOFAJ-UHFFFAOYSA-N n-butyl-n-(3-phenylprop-2-enyl)butan-1-amine Chemical compound CCCCN(CCCC)CC=CC1=CC=CC=C1 TTWJFBWTJAOFAJ-UHFFFAOYSA-N 0.000 description 1
- IVNQZTAKCPLGIP-UHFFFAOYSA-N n-butyl-n-[2-(3-phenylprop-2-enoxy)ethyl]butan-1-amine Chemical compound CCCCN(CCCC)CCOCC=CC1=CC=CC=C1 IVNQZTAKCPLGIP-UHFFFAOYSA-N 0.000 description 1
- KZXALWJOWSWIEU-UHFFFAOYSA-N n-dodecyl-n-(2-phenylethenyl)dodecan-1-amine Chemical compound CCCCCCCCCCCCN(CCCCCCCCCCCC)C=CC1=CC=CC=C1 KZXALWJOWSWIEU-UHFFFAOYSA-N 0.000 description 1
- CHHKYGYNEUBCAF-UHFFFAOYSA-N n-dodecyl-n-(3-phenylprop-2-enyl)dodecan-1-amine Chemical compound CCCCCCCCCCCCN(CCCCCCCCCCCC)CC=CC1=CC=CC=C1 CHHKYGYNEUBCAF-UHFFFAOYSA-N 0.000 description 1
- WBAMNCSDJQKWNM-UHFFFAOYSA-N n-ethyl-2-phenylethenamine Chemical compound CCNC=CC1=CC=CC=C1 WBAMNCSDJQKWNM-UHFFFAOYSA-N 0.000 description 1
- DIMUXHUOCLCTEV-UHFFFAOYSA-N n-ethyl-3-phenylprop-2-en-1-amine Chemical compound CCNCC=CC1=CC=CC=C1 DIMUXHUOCLCTEV-UHFFFAOYSA-N 0.000 description 1
- MCUPREGIRWCZLQ-UHFFFAOYSA-N n-ethyl-n-(2-phenylethenyl)aniline Chemical compound C=1C=CC=CC=1N(CC)C=CC1=CC=CC=C1 MCUPREGIRWCZLQ-UHFFFAOYSA-N 0.000 description 1
- ZEHPRMOGMMPUIN-UHFFFAOYSA-N n-ethyl-n-(2-phenylethenyl)anthracen-1-amine Chemical compound C=1C=CC2=CC3=CC=CC=C3C=C2C=1N(CC)C=CC1=CC=CC=C1 ZEHPRMOGMMPUIN-UHFFFAOYSA-N 0.000 description 1
- ACYGUOHCNODRSW-UHFFFAOYSA-N n-ethyl-n-(2-phenylethenyl)naphthalen-1-amine Chemical compound C=1C=CC2=CC=CC=C2C=1N(CC)C=CC1=CC=CC=C1 ACYGUOHCNODRSW-UHFFFAOYSA-N 0.000 description 1
- LOFLTXVHYVBYNR-UHFFFAOYSA-N n-ethyl-n-(2-phenylethenyl)phenanthren-1-amine Chemical compound C=1C=CC(C2=CC=CC=C2C=C2)=C2C=1N(CC)C=CC1=CC=CC=C1 LOFLTXVHYVBYNR-UHFFFAOYSA-N 0.000 description 1
- BNEFXFLBCVPKAZ-UHFFFAOYSA-N n-ethyl-n-(3-phenylprop-2-enyl)aniline Chemical compound C=1C=CC=CC=1N(CC)CC=CC1=CC=CC=C1 BNEFXFLBCVPKAZ-UHFFFAOYSA-N 0.000 description 1
- SQPBDUZHFXXJOH-UHFFFAOYSA-N n-ethyl-n-(3-phenylprop-2-enyl)anthracen-1-amine Chemical compound C=1C=CC2=CC3=CC=CC=C3C=C2C=1N(CC)CC=CC1=CC=CC=C1 SQPBDUZHFXXJOH-UHFFFAOYSA-N 0.000 description 1
- QBKDYUNPTCJWLX-UHFFFAOYSA-N n-ethyl-n-(3-phenylprop-2-enyl)naphthalen-1-amine Chemical compound C=1C=CC2=CC=CC=C2C=1N(CC)CC=CC1=CC=CC=C1 QBKDYUNPTCJWLX-UHFFFAOYSA-N 0.000 description 1
- ATNBQRMMPAAMAK-UHFFFAOYSA-N n-ethyl-n-(3-phenylprop-2-enyl)phenanthren-1-amine Chemical compound C=1C=CC(C2=CC=CC=C2C=C2)=C2C=1N(CC)CC=CC1=CC=CC=C1 ATNBQRMMPAAMAK-UHFFFAOYSA-N 0.000 description 1
- YRCITLUPWRTDDM-UHFFFAOYSA-N n-ethyl-n-[2-(3-phenylprop-2-enoxy)ethyl]aniline Chemical compound C=1C=CC=CC=1N(CC)CCOCC=CC1=CC=CC=C1 YRCITLUPWRTDDM-UHFFFAOYSA-N 0.000 description 1
- JXUPIBRLTLILIB-UHFFFAOYSA-N n-hexyl-n-(2-phenylethenyl)hexan-1-amine Chemical compound CCCCCCN(CCCCCC)C=CC1=CC=CC=C1 JXUPIBRLTLILIB-UHFFFAOYSA-N 0.000 description 1
- NCNWQVIJVIAHEY-UHFFFAOYSA-N n-hexyl-n-(3-phenylprop-2-enyl)hexan-1-amine Chemical compound CCCCCCN(CCCCCC)CC=CC1=CC=CC=C1 NCNWQVIJVIAHEY-UHFFFAOYSA-N 0.000 description 1
- JHWQVZVPLILUIM-UHFFFAOYSA-N n-methyl-2-(3-phenylprop-2-enoxy)ethanamine Chemical compound CNCCOCC=CC1=CC=CC=C1 JHWQVZVPLILUIM-UHFFFAOYSA-N 0.000 description 1
- CSEKTVJPPOKBEY-UHFFFAOYSA-N n-methyl-2-phenylethenamine Chemical compound CNC=CC1=CC=CC=C1 CSEKTVJPPOKBEY-UHFFFAOYSA-N 0.000 description 1
- RHPMSSCVPPONDM-UHFFFAOYSA-N n-methyl-3-phenylprop-2-en-1-amine Chemical compound CNCC=CC1=CC=CC=C1 RHPMSSCVPPONDM-UHFFFAOYSA-N 0.000 description 1
- WKXRVIFGACQFED-UHFFFAOYSA-N n-methyl-n-(2-phenylethenyl)aniline Chemical compound C=1C=CC=CC=1N(C)C=CC1=CC=CC=C1 WKXRVIFGACQFED-UHFFFAOYSA-N 0.000 description 1
- FYMQJTGNKFOYTD-UHFFFAOYSA-N n-methyl-n-(3-phenylprop-2-enyl)aniline Chemical compound C=1C=CC=CC=1N(C)CC=CC1=CC=CC=C1 FYMQJTGNKFOYTD-UHFFFAOYSA-N 0.000 description 1
- NSHYDDFRLRMWIA-UHFFFAOYSA-N n-methyl-n-[2-(3-phenylprop-2-enoxy)ethyl]aniline Chemical compound C=1C=CC=CC=1N(C)CCOCC=CC1=CC=CC=C1 NSHYDDFRLRMWIA-UHFFFAOYSA-N 0.000 description 1
- KOJVVMXIIKGIRV-UHFFFAOYSA-N n-octadecyl-n-(2-phenylethenyl)octadecan-1-amine Chemical compound CCCCCCCCCCCCCCCCCCN(CCCCCCCCCCCCCCCCCC)C=CC1=CC=CC=C1 KOJVVMXIIKGIRV-UHFFFAOYSA-N 0.000 description 1
- HMNLVJAACLFSOT-UHFFFAOYSA-N n-octadecyl-n-(3-phenylprop-2-enyl)octadecan-1-amine Chemical compound CCCCCCCCCCCCCCCCCCN(CCCCCCCCCCCCCCCCCC)CC=CC1=CC=CC=C1 HMNLVJAACLFSOT-UHFFFAOYSA-N 0.000 description 1
- GSZPZZQVYQGLRK-UHFFFAOYSA-N n-octyl-n-(2-phenylethenyl)octan-1-amine Chemical compound CCCCCCCCN(CCCCCCCC)C=CC1=CC=CC=C1 GSZPZZQVYQGLRK-UHFFFAOYSA-N 0.000 description 1
- ARVJBKOYSHWGCT-UHFFFAOYSA-N n-octyl-n-(3-phenylprop-2-enyl)octan-1-amine Chemical compound CCCCCCCCN(CCCCCCCC)CC=CC1=CC=CC=C1 ARVJBKOYSHWGCT-UHFFFAOYSA-N 0.000 description 1
- QPJHHONQEGCLDE-UHFFFAOYSA-N n-octyl-n-[2-(3-phenylprop-2-enoxy)ethyl]octan-1-amine Chemical compound CCCCCCCCN(CCCCCCCC)CCOCC=CC1=CC=CC=C1 QPJHHONQEGCLDE-UHFFFAOYSA-N 0.000 description 1
- 239000002736 nonionic surfactant Chemical class 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
- 235000014593 oils and fats 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
- 239000012860 organic pigment Substances 0.000 description 1
- 239000010452 phosphate Substances 0.000 description 1
- 150000003014 phosphoric acid esters Chemical class 0.000 description 1
- 230000036211 photosensitivity Effects 0.000 description 1
- 229920000647 polyepoxide Polymers 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 229920000098 polyolefin Polymers 0.000 description 1
- 235000013855 polyvinylpyrrolidone Nutrition 0.000 description 1
- 229920000036 polyvinylpyrrolidone Polymers 0.000 description 1
- 239000001267 polyvinylpyrrolidone Substances 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
- WVIICGIFSIBFOG-UHFFFAOYSA-N pyrylium Chemical class C1=CC=[O+]C=C1 WVIICGIFSIBFOG-UHFFFAOYSA-N 0.000 description 1
- 238000010992 reflux Methods 0.000 description 1
- 238000001226 reprecipitation Methods 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
- 229910052711 selenium Inorganic materials 0.000 description 1
- 239000011669 selenium Substances 0.000 description 1
- 239000008117 stearic acid Substances 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 238000003860 storage Methods 0.000 description 1
- 150000003440 styrenes Chemical class 0.000 description 1
- 150000005846 sugar alcohols Polymers 0.000 description 1
- 150000003460 sulfonic acids Chemical class 0.000 description 1
- 239000004094 surface-active agent Substances 0.000 description 1
- 238000010558 suspension polymerization method Methods 0.000 description 1
- 230000002194 synthesizing effect Effects 0.000 description 1
- 230000001988 toxicity Effects 0.000 description 1
- 231100000419 toxicity Toxicity 0.000 description 1
- RBKBGHZMNFTKRE-UHFFFAOYSA-K trisodium 2-[(2-oxido-3-sulfo-6-sulfonatonaphthalen-1-yl)diazenyl]benzoate Chemical compound C1=CC=C(C(=C1)C(=O)[O-])N=NC2=C3C=CC(=CC3=CC(=C2[O-])S(=O)(=O)O)S(=O)(=O)[O-].[Na+].[Na+].[Na+] RBKBGHZMNFTKRE-UHFFFAOYSA-K 0.000 description 1
- 229920001567 vinyl ester resin Polymers 0.000 description 1
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
- 239000011787 zinc oxide Substances 0.000 description 1
- 229910052984 zinc sulfide Inorganic materials 0.000 description 1
- DRDVZXDWVBGGMH-UHFFFAOYSA-N zinc;sulfide Chemical compound [S-2].[Zn+2] DRDVZXDWVBGGMH-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- G—PHYSICS
- G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
- G03G—ELECTROGRAPHY; ELECTROPHOTOGRAPHY; MAGNETOGRAPHY
- G03G9/00—Developers
- G03G9/08—Developers with toner particles
- G03G9/12—Developers with toner particles in liquid developer mixtures
- G03G9/13—Developers with toner particles in liquid developer mixtures characterised by polymer components
- G03G9/131—Developers with toner particles in liquid developer mixtures characterised by polymer components obtained by reactions only involving carbon-to-carbon unsaturated bonds
Landscapes
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Physics & Mathematics (AREA)
- General Physics & Mathematics (AREA)
- Liquid Developers In Electrophotography (AREA)
Priority Applications (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP60218600A JPS6278571A (ja) | 1985-10-01 | 1985-10-01 | 静電荷像用液体現像剤 |
| US06/913,277 US4734351A (en) | 1985-09-30 | 1986-09-30 | Liquid developer for electrostatic charge image |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP60218600A JPS6278571A (ja) | 1985-10-01 | 1985-10-01 | 静電荷像用液体現像剤 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS6278571A JPS6278571A (ja) | 1987-04-10 |
| JPH0582941B2 true JPH0582941B2 (enrdf_load_stackoverflow) | 1993-11-24 |
Family
ID=16722497
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP60218600A Granted JPS6278571A (ja) | 1985-09-30 | 1985-10-01 | 静電荷像用液体現像剤 |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS6278571A (enrdf_load_stackoverflow) |
-
1985
- 1985-10-01 JP JP60218600A patent/JPS6278571A/ja active Granted
Also Published As
| Publication number | Publication date |
|---|---|
| JPS6278571A (ja) | 1987-04-10 |
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