JPH0812490B2 - 静電写真用液体現像剤 - Google Patents

静電写真用液体現像剤

Info

Publication number: JPH0812490B2
Authority: JP; Japan
Prior art keywords: monomer; group; resin; same; general formula
Prior art date: 1986-01-20
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 - Fee Related

Application number

JP61009729A

Other languages

English (en)

Japanese (ja)

Other versions

JPS62166362A (ja

Inventor

栄一加藤

誠之團

寛石橋

一夫石井

英史世羅

Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)

Fujifilm Holdings Corp

Original Assignee

Fuji Photo Film Co Ltd

Priority date (The priority date 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 date listed.)

1986-01-20

Filing date

1986-01-20

Publication date

1996-02-07

1986-01-20 Application filed by Fuji Photo Film Co Ltd filed Critical Fuji Photo Film Co Ltd

1986-01-20 Priority to JP61009729A priority Critical patent/JPH0812490B2/ja

1987-01-20 Priority to DE19873701487 priority patent/DE3701487A1/de

1987-07-22 Publication of JPS62166362A publication Critical patent/JPS62166362A/ja

1996-02-07 Publication of JPH0812490B2 publication Critical patent/JPH0812490B2/ja

2011-02-07 Anticipated expiration legal-status Critical

Status Expired - Fee Related legal-status Critical Current

Links

239000007788 liquid Substances 0.000 title claims description 36
229920005989 resin Polymers 0.000 claims description 94
239000011347 resin Substances 0.000 claims description 94
239000000178 monomer Substances 0.000 claims description 81
125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 21
125000004432 carbon atom Chemical group C* 0.000 claims description 18
125000000217 alkyl group Chemical group 0.000 claims description 17
238000006116 polymerization reaction Methods 0.000 claims description 17
229920000642 polymer Polymers 0.000 claims description 13
239000003125 aqueous solvent Substances 0.000 claims description 10
239000002904 solvent Substances 0.000 claims description 10
239000003960 organic solvent Substances 0.000 claims description 9
150000002430 hydrocarbons Chemical class 0.000 claims description 8
-1 -OH Chemical group 0.000 claims description 7
229910052799 carbon Inorganic materials 0.000 claims description 7
125000005843 halogen group Chemical group 0.000 claims description 7
125000001931 aliphatic group Chemical group 0.000 claims description 6
125000005842 heteroatom Chemical group 0.000 claims description 5
125000005647 linker group Chemical group 0.000 claims description 5
229930195733 hydrocarbon Natural products 0.000 claims description 4
230000000379 polymerizing effect Effects 0.000 claims description 4
125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims description 3
229920006026 co-polymeric resin Polymers 0.000 claims description 3
125000000524 functional group Chemical group 0.000 claims description 3
239000004215 Carbon black (E152) Substances 0.000 claims description 2
125000004429 atom Chemical group 0.000 claims description 2
125000001183 hydrocarbyl group Chemical group 0.000 claims 6
239000002245 particle Substances 0.000 description 66
239000006185 dispersion Substances 0.000 description 61
238000004519 manufacturing process Methods 0.000 description 40
IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 24
238000000034 method Methods 0.000 description 24
SGVYKUFIHHTIFL-UHFFFAOYSA-N 2-methylnonane Chemical compound CCCCCCCC(C)C SGVYKUFIHHTIFL-UHFFFAOYSA-N 0.000 description 18
150000001875 compounds Chemical class 0.000 description 16
238000007639 printing Methods 0.000 description 16
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239000011259 mixed solution Substances 0.000 description 15
239000000243 solution Substances 0.000 description 15
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238000007645 offset printing Methods 0.000 description 10
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238000001816 cooling Methods 0.000 description 9
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239000007787 solid Substances 0.000 description 9
230000000087 stabilizing effect Effects 0.000 description 9
YAAYJRKCGZQWCB-UHFFFAOYSA-N 2-(1-cyanopropyldiazenyl)butanenitrile Chemical compound CCC(C#N)N=NC(CC)C#N YAAYJRKCGZQWCB-UHFFFAOYSA-N 0.000 description 8
XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 8
238000006243 chemical reaction Methods 0.000 description 8
230000000052 comparative effect Effects 0.000 description 8
SNRUBQQJIBEYMU-UHFFFAOYSA-N dodecane Chemical compound CCCCCCCCCCCC SNRUBQQJIBEYMU-UHFFFAOYSA-N 0.000 description 7
239000004816 latex Substances 0.000 description 7
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235000014113 dietary fatty acids Nutrition 0.000 description 6
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239000000194 fatty acid Substances 0.000 description 6
SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 5
NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 5
OMPJBNCRMGITSC-UHFFFAOYSA-N Benzoylperoxide Chemical compound C=1C=CC=CC=1C(=O)OOC(=O)C1=CC=CC=C1 OMPJBNCRMGITSC-UHFFFAOYSA-N 0.000 description 5
CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 description 5
WHNWPMSKXPGLAX-UHFFFAOYSA-N N-Vinyl-2-pyrrolidone Chemical compound C=CN1CCCC1=O WHNWPMSKXPGLAX-UHFFFAOYSA-N 0.000 description 5
125000003342 alkenyl group Chemical group 0.000 description 5
235000019400 benzoyl peroxide Nutrition 0.000 description 5
LDHQCZJRKDOVOX-NSCUHMNNSA-N crotonic acid Chemical compound C\C=C\C(O)=O LDHQCZJRKDOVOX-NSCUHMNNSA-N 0.000 description 5
238000011161 development Methods 0.000 description 5
238000007865 diluting Methods 0.000 description 5
239000000463 material Substances 0.000 description 5
239000000049 pigment Substances 0.000 description 5
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238000011105 stabilization Methods 0.000 description 5
LDHQCZJRKDOVOX-UHFFFAOYSA-N trans-crotonic acid Natural products CC=CC(O)=O LDHQCZJRKDOVOX-UHFFFAOYSA-N 0.000 description 5
238000012546 transfer Methods 0.000 description 5
CNPVJWYWYZMPDS-UHFFFAOYSA-N 2-methyldecane Chemical compound CCCCCCCCC(C)C CNPVJWYWYZMPDS-UHFFFAOYSA-N 0.000 description 4
PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 4
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 4
125000003710 aryl alkyl group Chemical group 0.000 description 4
DIOQZVSQGTUSAI-UHFFFAOYSA-N decane Chemical compound CCCCCCCCCC DIOQZVSQGTUSAI-UHFFFAOYSA-N 0.000 description 4
238000009826 distribution Methods 0.000 description 4
150000004665 fatty acids Chemical class 0.000 description 4
229910052751 metal Inorganic materials 0.000 description 4
239000002184 metal Substances 0.000 description 4
238000003860 storage Methods 0.000 description 4
FXNDIJDIPNCZQJ-UHFFFAOYSA-N 2,4,4-trimethylpent-1-ene Chemical group CC(=C)CC(C)(C)C FXNDIJDIPNCZQJ-UHFFFAOYSA-N 0.000 description 3
QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 3
OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
239000000654 additive Substances 0.000 description 3
150000001338 aliphatic hydrocarbons Chemical class 0.000 description 3
229920000180 alkyd Polymers 0.000 description 3
ZCGHEBMEQXMRQL-UHFFFAOYSA-N benzyl 2-carbamoylpyrrolidine-1-carboxylate Chemical compound NC(=O)C1CCCN1C(=O)OCC1=CC=CC=C1 ZCGHEBMEQXMRQL-UHFFFAOYSA-N 0.000 description 3
239000006229 carbon black Substances 0.000 description 3
150000001735 carboxylic acids Chemical class 0.000 description 3
239000003086 colorant Substances 0.000 description 3
125000004093 cyano group Chemical group *C#N 0.000 description 3
238000010438 heat treatment Methods 0.000 description 3
239000011976 maleic acid Substances 0.000 description 3
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 3
VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 3
229940094933 n-dodecane Drugs 0.000 description 3
239000000025 natural resin Substances 0.000 description 3
HMZGPNHSPWNGEP-UHFFFAOYSA-N octadecyl 2-methylprop-2-enoate Chemical compound CCCCCCCCCCCCCCCCCCOC(=O)C(C)=C HMZGPNHSPWNGEP-UHFFFAOYSA-N 0.000 description 3
239000003208 petroleum Substances 0.000 description 3
150000003839 salts Chemical class 0.000 description 3
229920003002 synthetic resin Polymers 0.000 description 3
239000000057 synthetic resin Substances 0.000 description 3
229920002818 (Hydroxyethyl)methacrylate Polymers 0.000 description 2
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 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
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 2
OMIGHNLMNHATMP-UHFFFAOYSA-N 2-hydroxyethyl prop-2-enoate Chemical compound OCCOC(=O)C=C OMIGHNLMNHATMP-UHFFFAOYSA-N 0.000 description 2
GTJOHISYCKPIMT-UHFFFAOYSA-N 2-methylundecane Chemical compound CCCCCCCCCC(C)C GTJOHISYCKPIMT-UHFFFAOYSA-N 0.000 description 2
NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 description 2
KAKZBPTYRLMSJV-UHFFFAOYSA-N Butadiene Chemical compound C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 description 2
FERIUCNNQQJTOY-UHFFFAOYSA-N Butyric acid Chemical compound CCCC(O)=O FERIUCNNQQJTOY-UHFFFAOYSA-N 0.000 description 2
WOBHKFSMXKNTIM-UHFFFAOYSA-N Hydroxyethyl methacrylate Chemical compound CC(=C)C(=O)OCCO WOBHKFSMXKNTIM-UHFFFAOYSA-N 0.000 description 2
UQSXHKLRYXJYBZ-UHFFFAOYSA-N Iron oxide Chemical compound [Fe]=O UQSXHKLRYXJYBZ-UHFFFAOYSA-N 0.000 description 2
NHTMVDHEPJAVLT-UHFFFAOYSA-N Isooctane Chemical compound CC(C)CC(C)(C)C NHTMVDHEPJAVLT-UHFFFAOYSA-N 0.000 description 2
RRHGJUQNOFWUDK-UHFFFAOYSA-N Isoprene Chemical compound CC(=C)C=C RRHGJUQNOFWUDK-UHFFFAOYSA-N 0.000 description 2
MZRVEZGGRBJDDB-UHFFFAOYSA-N N-Butyllithium Chemical compound [Li]CCCC MZRVEZGGRBJDDB-UHFFFAOYSA-N 0.000 description 2
OFOBLEOULBTSOW-UHFFFAOYSA-N Propanedioic acid Natural products OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 2
235000010724 Wisteria floribunda Nutrition 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
150000007513 acids Chemical class 0.000 description 2
125000002723 alicyclic group Chemical group 0.000 description 2
125000005907 alkyl ester group Chemical group 0.000 description 2
XYLMUPLGERFSHI-UHFFFAOYSA-N alpha-Methylstyrene Chemical compound CC(=C)C1=CC=CC=C1 XYLMUPLGERFSHI-UHFFFAOYSA-N 0.000 description 2
230000009435 amidation Effects 0.000 description 2
238000007112 amidation reaction Methods 0.000 description 2
125000003277 amino group Chemical group 0.000 description 2
150000008064 anhydrides Chemical class 0.000 description 2
150000004945 aromatic hydrocarbons Chemical class 0.000 description 2
239000011324 bead Substances 0.000 description 2
150000001721 carbon Chemical group 0.000 description 2
239000003795 chemical substances by application Substances 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
239000000470 constituent Substances 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
NNBZCPXTIHJBJL-UHFFFAOYSA-N decalin Chemical compound C1CCCC2CCCCC21 NNBZCPXTIHJBJL-UHFFFAOYSA-N 0.000 description 2
JVSWJIKNEAIKJW-UHFFFAOYSA-N dimethyl-hexane Natural products CCCCCC(C)C JVSWJIKNEAIKJW-UHFFFAOYSA-N 0.000 description 2
XBDQKXXYIPTUBI-UHFFFAOYSA-N dimethylselenoniopropionate Natural products CCC(O)=O XBDQKXXYIPTUBI-UHFFFAOYSA-N 0.000 description 2
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VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 description 2
FPYJFEHAWHCUMM-UHFFFAOYSA-N maleic anhydride Chemical compound O=C1OC(=O)C=C1 FPYJFEHAWHCUMM-UHFFFAOYSA-N 0.000 description 2
QYZFTMMPKCOTAN-UHFFFAOYSA-N n-[2-(2-hydroxyethylamino)ethyl]-2-[[1-[2-(2-hydroxyethylamino)ethylamino]-2-methyl-1-oxopropan-2-yl]diazenyl]-2-methylpropanamide Chemical compound OCCNCCNC(=O)C(C)(C)N=NC(C)(C)C(=O)NCCNCCO QYZFTMMPKCOTAN-UHFFFAOYSA-N 0.000 description 2
125000004433 nitrogen atom Chemical group N* 0.000 description 2
ZCYXXKJEDCHMGH-UHFFFAOYSA-N nonane Chemical compound CCCC[CH]CCCC ZCYXXKJEDCHMGH-UHFFFAOYSA-N 0.000 description 2
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150000003440 styrenes Chemical class 0.000 description 2
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JAHNSTQSQJOJLO-UHFFFAOYSA-N 2-(3-fluorophenyl)-1h-imidazole Chemical compound FC1=CC=CC(C=2NC=CN=2)=C1 JAHNSTQSQJOJLO-UHFFFAOYSA-N 0.000 description 1
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125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 description 1
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125000002947 alkylene group Chemical group 0.000 description 1
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230000015572 biosynthetic process Effects 0.000 description 1
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125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 description 1
125000001309 chloro group Chemical group Cl* 0.000 description 1
FOCAUTSVDIKZOP-UHFFFAOYSA-N chloroacetic acid Chemical compound OC(=O)CCl FOCAUTSVDIKZOP-UHFFFAOYSA-N 0.000 description 1
239000011362 coarse particle Substances 0.000 description 1
238000007334 copolymerization reaction Methods 0.000 description 1
238000004132 cross linking Methods 0.000 description 1
125000000753 cycloalkyl group Chemical group 0.000 description 1
GTBGXKPAKVYEKJ-UHFFFAOYSA-N decyl 2-methylprop-2-enoate Chemical compound CCCCCCCCCCOC(=O)C(C)=C GTBGXKPAKVYEKJ-UHFFFAOYSA-N 0.000 description 1
238000004043 dyeing Methods 0.000 description 1
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238000002474 experimental method Methods 0.000 description 1
238000001879 gelation Methods 0.000 description 1
238000004128 high performance liquid chromatography Methods 0.000 description 1
239000012456 homogeneous solution Substances 0.000 description 1
XMBWDFGMSWQBCA-UHFFFAOYSA-N hydrogen iodide Chemical compound I XMBWDFGMSWQBCA-UHFFFAOYSA-N 0.000 description 1
239000003999 initiator Substances 0.000 description 1
239000001023 inorganic pigment Substances 0.000 description 1
238000009413 insulation Methods 0.000 description 1
125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
150000002689 maleic acids Chemical class 0.000 description 1
LVHBHZANLOWSRM-UHFFFAOYSA-N methylenebutanedioic acid Natural products OC(=O)CC(=C)C(O)=O LVHBHZANLOWSRM-UHFFFAOYSA-N 0.000 description 1
125000004123 n-propyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
239000003921 oil Substances 0.000 description 1
235000019198 oils Nutrition 0.000 description 1
JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 description 1
239000012860 organic pigment Substances 0.000 description 1
229920005749 polyurethane resin Polymers 0.000 description 1
239000000843 powder Substances 0.000 description 1
235000019260 propionic acid Nutrition 0.000 description 1
IUVKMZGDUIUOCP-BTNSXGMBSA-N quinbolone Chemical compound O([C@H]1CC[C@H]2[C@H]3[C@@H]([C@]4(C=CC(=O)C=C4CC3)C)CC[C@@]21C)C1=CCCC1 IUVKMZGDUIUOCP-BTNSXGMBSA-N 0.000 description 1
238000007348 radical reaction Methods 0.000 description 1
238000004062 sedimentation Methods 0.000 description 1
230000035945 sensitivity Effects 0.000 description 1
239000000344 soap Substances 0.000 description 1
230000007928 solubilization Effects 0.000 description 1
238000005063 solubilization Methods 0.000 description 1
235000015096 spirit Nutrition 0.000 description 1
230000002269 spontaneous effect Effects 0.000 description 1
125000001424 substituent group Chemical group 0.000 description 1
125000000542 sulfonic acid group Chemical group 0.000 description 1
239000002344 surface layer Substances 0.000 description 1
229920003051 synthetic elastomer Polymers 0.000 description 1
239000005061 synthetic rubber Substances 0.000 description 1
230000001988 toxicity Effects 0.000 description 1
231100000419 toxicity Toxicity 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
PXXNTAGJWPJAGM-UHFFFAOYSA-N vertaline Natural products C1C2C=3C=C(OC)C(OC)=CC=3OC(C=C3)=CC=C3CCC(=O)OC1CC1N2CCCC1 PXXNTAGJWPJAGM-UHFFFAOYSA-N 0.000 description 1
LLWJPGAKXJBKKA-UHFFFAOYSA-N victoria blue B Chemical compound [Cl-].C1=CC(N(C)C)=CC=C1C(C=1C=CC(=CC=1)N(C)C)=C(C=C1)C2=CC=CC=C2C1=[NH+]C1=CC=CC=C1 LLWJPGAKXJBKKA-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
239000011345 viscous material Substances 0.000 description 1
239000011787 zinc oxide Substances 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)

JP61009729A 1986-01-20 1986-01-20 静電写真用液体現像剤 Expired - Fee Related JPH0812490B2 (ja)

Priority Applications (2)

Application Number	Priority Date	Filing Date	Title
JP61009729A JPH0812490B2 (ja)	1986-01-20	1986-01-20	静電写真用液体現像剤
DE19873701487 DE3701487A1 (de)	1986-01-20	1987-01-20	Elektrostatographischer suspensionsentwickler

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
JP61009729A JPH0812490B2 (ja)	1986-01-20	1986-01-20	静電写真用液体現像剤

Publications (2)

Publication Number	Publication Date
JPS62166362A JPS62166362A (ja)	1987-07-22
JPH0812490B2 true JPH0812490B2 (ja)	1996-02-07

Family

ID=11728400

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
JP61009729A Expired - Fee Related JPH0812490B2 (ja)	1986-01-20	1986-01-20	静電写真用液体現像剤

Country Status (2)

Country	Link
JP (1)	JPH0812490B2 (de)
DE (1)	DE3701487A1 (de)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
CN108064253A (zh) *	2015-07-02	2018-05-22	生命技术公司	由羧基官能丙烯酰胺形成的聚合物基质

Families Citing this family (4)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
JP2614051B2 (ja) *	1987-09-07	1997-05-28	富士写真フイルム株式会社	電子写真用液体現像剤の製造法
JP2752621B2 (ja) *	1987-09-09	1998-05-18	文化シャッター株式会社	シャッタの管理制御装置
JPH02116859A (ja) *	1988-10-27	1990-05-01	Fuji Photo Film Co Ltd	静電写真用液体現像剤
DE68925353T2 (de) *	1988-12-27	1996-06-13	Fuji Photo Film Co Ltd	Flüssiger Entwickler für elektrostatische Photographie

Family Cites Families (1)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
JPS60185963A (ja) *	1984-03-05	1985-09-21	Fuji Photo Film Co Ltd	静電写真用液体現像剤

1986
- 1986-01-20 JP JP61009729A patent/JPH0812490B2/ja not_active Expired - Fee Related
1987
- 1987-01-20 DE DE19873701487 patent/DE3701487A1/de not_active Withdrawn

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
CN108064253A (zh) *	2015-07-02	2018-05-22	生命技术公司	由羧基官能丙烯酰胺形成的聚合物基质
CN108064253B (zh) *	2015-07-02	2020-09-15	生命技术公司	由羧基官能丙烯酰胺形成的聚合物基质

Also Published As

Publication number	Publication date
JPS62166362A (ja)	1987-07-22
DE3701487A1 (de)	1987-07-23

Publication	Publication Date	Title
JPH0431109B2 (de)	1992-05-25
US4665002A (en)	1987-05-12	Liquid developer for electrostatic photography
JPH0640229B2 (ja)	1994-05-25	静電写真用液体現像剤
JPH0629994B2 (ja)	1994-04-20	静電写真用液体現像剤
JP3567238B2 (ja)	2004-09-22	静電写真用の液体現像剤
JPH0812490B2 (ja)	1996-02-07	静電写真用液体現像剤
JPS6325665A (ja)	1988-02-03	液体静電現像剤用の帯電可能な樹脂
JPH0417430B2 (de)	1992-03-25
JPH01237668A (ja)	1989-09-22	静電写真用液体現像剤
JPS60185962A (ja)	1985-09-21	静電写真用液体現像剤
JPH0812491B2 (ja)	1996-02-07	静電写真用液体現像剤
JPS6015063B2 (ja)	1985-04-17	電子写真用混合液体ト−ナ−
JPS616662A (ja)	1986-01-13	静電写真用液体現像剤
JPH0431108B2 (de)	1992-05-25
JP3057510B2 (ja)	2000-06-26	静電潜像現像用湿式現像剤
JP2614038B2 (ja)	1997-05-28	静電写真用液体現像剤
JP2597187B2 (ja)	1997-04-02	静電写真用液体現像剤
JPS63110463A (ja)	1988-05-14	静電写真用液体現像剤
JPH087470B2 (ja)	1996-01-29	静電写真用液体現像剤
JP2822245B2 (ja)	1998-11-11	静電潜像現像用湿式現像剤
JPS61217069A (ja)	1986-09-26	静電写真用液体現像剤
JP2652237B2 (ja)	1997-09-10	静電写真用液体現像剤
JP2655348B2 (ja)	1997-09-17	静電写真用液体現像剤
JPH02103057A (ja)	1990-04-16	静電写真用液体現像剤
JP3158463B2 (ja)	2001-04-23	静電写真用液体現像剤

Legal Events

Date	Code	Title	Description
2004-02-07	LAPS	Cancellation because of no payment of annual fees