JPH03200978A - Developer - Google Patents
DeveloperInfo
- Publication number
- JPH03200978A JPH03200978A JP2049513A JP4951390A JPH03200978A JP H03200978 A JPH03200978 A JP H03200978A JP 2049513 A JP2049513 A JP 2049513A JP 4951390 A JP4951390 A JP 4951390A JP H03200978 A JPH03200978 A JP H03200978A
- Authority
- JP
- Japan
- Prior art keywords
- carrier
- developer
- toner
- resin
- range
- 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
- 239000011248 coating agent Substances 0.000 claims abstract description 22
- 238000000576 coating method Methods 0.000 claims abstract description 22
- 229920002050 silicone resin Polymers 0.000 claims abstract description 11
- 239000002245 particle Substances 0.000 claims description 46
- 108091008695 photoreceptors Proteins 0.000 claims description 42
- 150000001412 amines Chemical class 0.000 claims description 13
- 239000011162 core material Substances 0.000 claims description 5
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 claims description 4
- OGIDPMRJRNCKJF-UHFFFAOYSA-N titanium oxide Inorganic materials [Ti]=O OGIDPMRJRNCKJF-UHFFFAOYSA-N 0.000 claims description 4
- 229920005989 resin Polymers 0.000 abstract description 28
- 239000011347 resin Substances 0.000 abstract description 28
- 238000005513 bias potential Methods 0.000 description 19
- 239000000049 pigment Substances 0.000 description 16
- 239000003086 colorant Substances 0.000 description 13
- 239000000969 carrier Substances 0.000 description 9
- 229910000859 α-Fe Inorganic materials 0.000 description 9
- 239000003795 chemical substances by application Substances 0.000 description 8
- 241000254158 Lampyridae Species 0.000 description 6
- 241000519995 Stachys sylvatica Species 0.000 description 6
- 239000010410 layer Substances 0.000 description 6
- 239000000463 material Substances 0.000 description 6
- 238000009826 distribution Methods 0.000 description 5
- 229920001296 polysiloxane Polymers 0.000 description 5
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 description 4
- 238000010586 diagram Methods 0.000 description 4
- 229910052751 metal Inorganic materials 0.000 description 4
- 239000002184 metal Substances 0.000 description 4
- 238000000034 method Methods 0.000 description 4
- 239000011669 selenium Substances 0.000 description 4
- 229910052710 silicon Inorganic materials 0.000 description 4
- 239000010703 silicon Substances 0.000 description 4
- 229920000178 Acrylic resin Polymers 0.000 description 3
- 239000004925 Acrylic resin Substances 0.000 description 3
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 3
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 3
- 238000005520 cutting process Methods 0.000 description 3
- 239000011572 manganese Substances 0.000 description 3
- 230000000704 physical effect Effects 0.000 description 3
- 239000002904 solvent Substances 0.000 description 3
- RSWGJHLUYNHPMX-UHFFFAOYSA-N Abietic-Saeure Natural products C12CCC(C(C)C)=CC2=CCC2C1(C)CCCC2(C)C(O)=O RSWGJHLUYNHPMX-UHFFFAOYSA-N 0.000 description 2
- 229910000805 Pig iron Inorganic materials 0.000 description 2
- XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 description 2
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 2
- QVQLCTNNEUAWMS-UHFFFAOYSA-N barium oxide Chemical compound [Ba]=O QVQLCTNNEUAWMS-UHFFFAOYSA-N 0.000 description 2
- WGQKYBSKWIADBV-UHFFFAOYSA-N benzylamine Chemical compound NCC1=CC=CC=C1 WGQKYBSKWIADBV-UHFFFAOYSA-N 0.000 description 2
- 235000013339 cereals Nutrition 0.000 description 2
- 238000011109 contamination Methods 0.000 description 2
- 239000012050 conventional carrier Substances 0.000 description 2
- 230000006866 deterioration Effects 0.000 description 2
- 210000005069 ears Anatomy 0.000 description 2
- 230000005415 magnetization Effects 0.000 description 2
- 229910052748 manganese Inorganic materials 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- 229910052759 nickel Inorganic materials 0.000 description 2
- 239000000843 powder Substances 0.000 description 2
- 150000003839 salts Chemical class 0.000 description 2
- 229910052711 selenium Inorganic materials 0.000 description 2
- 239000000344 soap Substances 0.000 description 2
- JIAARYAFYJHUJI-UHFFFAOYSA-L zinc dichloride Chemical compound [Cl-].[Cl-].[Zn+2] JIAARYAFYJHUJI-UHFFFAOYSA-L 0.000 description 2
- SMKKEOQDQNCTGL-ZETCQYMHSA-N (2s)-2-[(2-nitrophenoxy)methyl]oxirane Chemical compound [O-][N+](=O)C1=CC=CC=C1OC[C@H]1OC1 SMKKEOQDQNCTGL-ZETCQYMHSA-N 0.000 description 1
- DZNJMLVCIZGWSC-UHFFFAOYSA-N 3',6'-bis(diethylamino)spiro[2-benzofuran-3,9'-xanthene]-1-one Chemical compound O1C(=O)C2=CC=CC=C2C21C1=CC=C(N(CC)CC)C=C1OC1=CC(N(CC)CC)=CC=C21 DZNJMLVCIZGWSC-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
- QMPUCZGGNKXEQF-UHFFFAOYSA-N 4-cyclohexyl-2-[[4-[1-[4-[(5-cyclohexyl-2-hydroxyphenyl)diazenyl]-3-methylphenyl]cyclohexyl]-2-methylphenyl]diazenyl]phenol Chemical compound C1(CCCCC1)(C1=CC(=C(C=C1)N=NC1=C(C=CC(=C1)C1CCCCC1)O)C)C1=CC(=C(C=C1)N=NC1=C(C=CC(=C1)C1CCCCC1)O)C QMPUCZGGNKXEQF-UHFFFAOYSA-N 0.000 description 1
- XCKGFJPFEHHHQA-UHFFFAOYSA-N 5-methyl-2-phenyl-4-phenyldiazenyl-4h-pyrazol-3-one Chemical compound CC1=NN(C=2C=CC=CC=2)C(=O)C1N=NC1=CC=CC=C1 XCKGFJPFEHHHQA-UHFFFAOYSA-N 0.000 description 1
- VJUKWPOWHJITTP-UHFFFAOYSA-N 81-39-0 Chemical compound C1=CC(C)=CC=C1NC1=CC=C2C3=C1C(=O)C1=CC=CC=C1C3=CC(=O)N2C VJUKWPOWHJITTP-UHFFFAOYSA-N 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- 229910052688 Gadolinium Inorganic materials 0.000 description 1
- UQSXHKLRYXJYBZ-UHFFFAOYSA-N Iron oxide Chemical compound [Fe]=O UQSXHKLRYXJYBZ-UHFFFAOYSA-N 0.000 description 1
- PWHULOQIROXLJO-UHFFFAOYSA-N Manganese Chemical compound [Mn] PWHULOQIROXLJO-UHFFFAOYSA-N 0.000 description 1
- 239000004952 Polyamide Substances 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
- BUGBHKTXTAQXES-UHFFFAOYSA-N Selenium Chemical compound [Se] BUGBHKTXTAQXES-UHFFFAOYSA-N 0.000 description 1
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 1
- 229910001035 Soft ferrite Inorganic materials 0.000 description 1
- 241000209140 Triticum Species 0.000 description 1
- 235000021307 Triticum Nutrition 0.000 description 1
- 239000005083 Zinc sulfide Substances 0.000 description 1
- JHNCXGXWSIOXSX-UHFFFAOYSA-N [Nd+3].[O-2].[Fe+2] Chemical compound [Nd+3].[O-2].[Fe+2] JHNCXGXWSIOXSX-UHFFFAOYSA-N 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- -1 acrylic silicon Chemical class 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 150000003973 alkyl amines Chemical class 0.000 description 1
- 229910021417 amorphous silicon Inorganic materials 0.000 description 1
- GHPGOEFPKIHBNM-UHFFFAOYSA-N antimony(3+);oxygen(2-) Chemical compound [O-2].[O-2].[O-2].[Sb+3].[Sb+3] GHPGOEFPKIHBNM-UHFFFAOYSA-N 0.000 description 1
- 150000004982 aromatic amines Chemical class 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- 239000000987 azo dye Substances 0.000 description 1
- 239000011230 binding agent Substances 0.000 description 1
- 230000008033 biological extinction Effects 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 229910052980 cadmium sulfide Inorganic materials 0.000 description 1
- BAXLMRUQFAMMQC-UHFFFAOYSA-N cadmium(2+) iron(2+) oxygen(2-) Chemical compound [Cd+2].[O-2].[Fe+2].[O-2] BAXLMRUQFAMMQC-UHFFFAOYSA-N 0.000 description 1
- UHYPYGJEEGLRJD-UHFFFAOYSA-N cadmium(2+);selenium(2-) Chemical compound [Se-2].[Cd+2] UHYPYGJEEGLRJD-UHFFFAOYSA-N 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 239000012876 carrier material Substances 0.000 description 1
- 229920006026 co-polymeric resin Polymers 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 238000013329 compounding Methods 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 229910052802 copper Inorganic materials 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
- 230000003247 decreasing effect Effects 0.000 description 1
- 230000007547 defect Effects 0.000 description 1
- 235000014113 dietary fatty acids Nutrition 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- ZBFOLPMOGPIUGP-UHFFFAOYSA-N dizinc;oxygen(2-);titanium(4+) Chemical compound [O-2].[O-2].[O-2].[O-2].[Ti+4].[Zn+2].[Zn+2] ZBFOLPMOGPIUGP-UHFFFAOYSA-N 0.000 description 1
- 239000000975 dye Substances 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 239000000194 fatty acid Substances 0.000 description 1
- 229930195729 fatty acid Natural products 0.000 description 1
- 150000004665 fatty acids Chemical class 0.000 description 1
- UIWYJDYFSGRHKR-UHFFFAOYSA-N gadolinium atom Chemical compound [Gd] UIWYJDYFSGRHKR-UHFFFAOYSA-N 0.000 description 1
- 230000009477 glass transition Effects 0.000 description 1
- 230000005484 gravity Effects 0.000 description 1
- 229910052736 halogen Inorganic materials 0.000 description 1
- 150000002367 halogens Chemical class 0.000 description 1
- 229930195733 hydrocarbon Natural products 0.000 description 1
- 150000002430 hydrocarbons Chemical class 0.000 description 1
- 230000002209 hydrophobic effect Effects 0.000 description 1
- 230000006698 induction Effects 0.000 description 1
- MHKWSJBPFXBFMX-UHFFFAOYSA-N iron magnesium Chemical compound [Mg].[Fe] MHKWSJBPFXBFMX-UHFFFAOYSA-N 0.000 description 1
- JEIPFZHSYJVQDO-UHFFFAOYSA-N iron(III) oxide Inorganic materials O=[Fe]O[Fe]=O JEIPFZHSYJVQDO-UHFFFAOYSA-N 0.000 description 1
- 229910052746 lanthanum Inorganic materials 0.000 description 1
- FZLIPJUXYLNCLC-UHFFFAOYSA-N lanthanum atom Chemical compound [La] FZLIPJUXYLNCLC-UHFFFAOYSA-N 0.000 description 1
- 229910000464 lead oxide Inorganic materials 0.000 description 1
- 229910052749 magnesium Inorganic materials 0.000 description 1
- 239000011777 magnesium Substances 0.000 description 1
- 239000000155 melt Substances 0.000 description 1
- 239000011859 microparticle Substances 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 239000000178 monomer Substances 0.000 description 1
- VKWNTWQXVLKCSG-UHFFFAOYSA-N n-ethyl-1-[(4-phenyldiazenylphenyl)diazenyl]naphthalen-2-amine Chemical compound CCNC1=CC=C2C=CC=CC2=C1N=NC(C=C1)=CC=C1N=NC1=CC=CC=C1 VKWNTWQXVLKCSG-UHFFFAOYSA-N 0.000 description 1
- 239000003921 oil Substances 0.000 description 1
- 230000003287 optical effect Effects 0.000 description 1
- 239000012860 organic pigment Substances 0.000 description 1
- 230000001151 other effect Effects 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- YEXPOXQUZXUXJW-UHFFFAOYSA-N oxolead Chemical compound [Pb]=O YEXPOXQUZXUXJW-UHFFFAOYSA-N 0.000 description 1
- 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 1
- 229940067265 pigment yellow 138 Drugs 0.000 description 1
- 229920000058 polyacrylate Polymers 0.000 description 1
- 229920002647 polyamide Polymers 0.000 description 1
- 229920001225 polyester resin Polymers 0.000 description 1
- 239000004645 polyester resin Substances 0.000 description 1
- 238000006116 polymerization reaction Methods 0.000 description 1
- 229920005749 polyurethane resin Polymers 0.000 description 1
- 239000011253 protective coating Substances 0.000 description 1
- 238000010298 pulverizing process Methods 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 125000003748 selenium group Chemical group *[Se]* 0.000 description 1
- 239000002356 single layer Substances 0.000 description 1
- 238000005245 sintering Methods 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 239000012798 spherical particle Substances 0.000 description 1
- LXMSZDCAJNLERA-ZHYRCANASA-N spironolactone Chemical compound C([C@@H]1[C@]2(C)CC[C@@H]3[C@@]4(C)CCC(=O)C=C4C[C@H]([C@@H]13)SC(=O)C)C[C@@]21CCC(=O)O1 LXMSZDCAJNLERA-ZHYRCANASA-N 0.000 description 1
- 229920001909 styrene-acrylic polymer Polymers 0.000 description 1
- 229920005792 styrene-acrylic resin Polymers 0.000 description 1
- 239000012756 surface treatment agent Substances 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
- 238000011144 upstream manufacturing Methods 0.000 description 1
- 239000012463 white pigment Substances 0.000 description 1
- 239000001060 yellow colorant Substances 0.000 description 1
- 239000001052 yellow pigment Substances 0.000 description 1
- 229910052725 zinc Inorganic materials 0.000 description 1
- 239000011701 zinc Substances 0.000 description 1
- 239000011592 zinc chloride Substances 0.000 description 1
- 235000005074 zinc chloride Nutrition 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
- G03G9/0821—Developers with toner particles characterised by physical parameters
- G03G9/0823—Electric parameters
-
- 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
- G03G9/10—Developers with toner particles characterised by carrier particles
- G03G9/113—Developers with toner particles characterised by carrier particles having coatings applied thereto
- G03G9/1132—Macromolecular components of coatings
- G03G9/1135—Macromolecular components of coatings obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
- G03G9/1136—Macromolecular components of coatings obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds containing silicon atoms
Abstract
Description
【発明の詳細な説明】
(産業上の利用分野)
本発明は電子複写等の現像、剤に関するものであり、よ
り詳細には、 トナーと磁性キャリヤとから成る二成分
系の現像剤であって、導電率の低いトナーを用いた場合
であっても高濃度画像が良好に得られる現像剤に関する
。[Detailed Description of the Invention] (Industrial Application Field) The present invention relates to a developer and agent for electronic copying, etc., and more specifically to a two-component developer consisting of a toner and a magnetic carrier. , relates to a developer that can produce high-density images satisfactorily even when using toner with low conductivity.
(従来技術)
商業的な電子複写の分野では、静電像の現像に、二成分
系磁性現像剤を用いる磁気ブラシ現像が広く使用されて
いる。二成分系磁性現像剤としては。(Prior Art) In the field of commercial electronic copying, magnetic brush development using a two-component magnetic developer is widely used to develop electrostatic images. As a two-component magnetic developer.
銖粉或いは焼結フェライト粒子等から成る磁性キャリヤ
と、定着性樹脂中に着色剤、電荷制御剤等の配合剤を分
散させて戒るトナー粒子との混合物が広く使用されてい
る。A mixture of a magnetic carrier made of powder, sintered ferrite particles, etc., and toner particles in which additives such as a colorant and a charge control agent are dispersed in a fixing resin is widely used.
現像剤が用いられる通常の現像機構部としては、第1図
に糸すような構造となっており、現像機構部2にはボッ
クス状のトナー供給機構4が設けられ、その上方からト
ナー6が供給される。 トナー6はフィーダー付き供給
口8を介して下方の現像器10内に供給され、現像器1
0内のキャリヤと共に撹拌機12.12によって撹拌さ
れて二成分系現像剤14を形威している。A normal developing mechanism section that uses developer has a structure as shown in FIG. Supplied. The toner 6 is supplied into the lower developing device 10 through the supply port 8 with a feeder, and the toner 6 is supplied into the developing device 10 below.
A two-component developer 14 is formed by being agitated with the carrier in the developer 12 by an agitator 12.12.
現像1)10内には多数の極磁を備えた現像スリーブ(
現像剤担持体)16が配せられ、現像スリーブ16には
トナーが摩擦電荷を得たのちの現像剤14が供給され、
更にスリーブ表面には現像剤によって磁気ブラシ18が
形威される。Ia&気ブラシ18は穂切り機構20によ
って穂立長が調整され、電子写真感光体ドラム(Ik担
持体)22の表面感光層24とのニップ位置まで搬送さ
れる。感光体ドラム22は現像スリーブ16からの距離
Do−sを置いて配せられ、現像スリーブ16及び感光
体ドラム22は撹拌(図示せず)に回転可能に支持され
てニップ位置における移動方向(矢印)が同方向(回転
方向は互いに逆方向)となるように能動される。Development 1) Inside the development sleeve 10 is a development sleeve (
A developer carrying member) 16 is disposed, and the developer 14 after the toner has acquired a triboelectric charge is supplied to the developing sleeve 16.
Furthermore, a magnetic brush 18 is formed on the sleeve surface by the developer. The Ia & air brush 18 is adjusted in its standing length by the ear cutting mechanism 20, and is conveyed to the nip position with the surface photosensitive layer 24 of the electrophotographic photosensitive drum (Ik carrier) 22. The photosensitive drum 22 is arranged at a distance Do-s from the developing sleeve 16, and the developing sleeve 16 and the photosensitive drum 22 are rotatably supported by an agitator (not shown) and are moved in the direction of movement (arrow) at the nip position. ) are activated so that they are in the same direction (rotation directions are opposite to each other).
感光体ドラム22の周囲には、可変高電圧電源24に接
続されたコロナチャージャー26及び露光用光学系28
が前記現像器10の上流側に配せられて所定の表面電位
の静電潜像を形成し得るようになっている。また、感光
ドラム22と現像スリーブ12との間には、電圧調節機
構30を備えたバイアス電[33が接続され、感光層2
4上に表面電位と同極でしかも該表面電位よりも低い任
意の411 (バイアス電位)が印加できる様になって
いる。更に、感光層24の周囲で現Ik部の下流にはト
ナー餘を複写機に転写するための転写機構34が設けら
れている。A corona charger 26 connected to a variable high voltage power supply 24 and an exposure optical system 28 are arranged around the photoreceptor drum 22.
is disposed upstream of the developing device 10 to form an electrostatic latent image with a predetermined surface potential. Furthermore, a bias voltage 33 equipped with a voltage adjustment mechanism 30 is connected between the photosensitive drum 22 and the developing sleeve 12, and the photosensitive layer 2
An arbitrary bias potential 411 (bias potential) which is the same polarity as the surface potential and lower than the surface potential can be applied to the surface potential. Further, a transfer mechanism 34 is provided around the photosensitive layer 24 and downstream of the current Ik portion for transferring the toner mass to the copying machine.
このような構成において、現像剤14は現像スリーブ1
8上で磁気ブラシ18を形威し、ニップ位置で感光層2
4の静電潜像と反応して感光層24上にトナーの可視1
&36を形式する。形成可視像36は転写機構34で転
写材に転写し、次いでトナー懺を定着することにより直
像形式を行っている。In such a configuration, the developer 14 is transferred to the developing sleeve 1.
Apply a magnetic brush 18 on the photosensitive layer 2 at the nip position.
A visible toner 1 is formed on the photosensitive layer 24 by reacting with the electrostatic latent image 4.
Format &36. The formed visible image 36 is transferred to a transfer material by a transfer mechanism 34, and then the toner smear is fixed, thereby performing a direct image format.
(発明が解決しようとする課題〉
ところで1両会形成に際しては、カーボン等の黒色顔料
に比べて、白色トナーや有彩色トナーに使用される酸化
チタンや有彩色顔料等は、電気抵抗(導電率の逆)が高
<、シかもその帯電量が多くなる傾向にあり、 トナー
の画像濃度(1,D)を高濃度に維持できない場合が生
じる。従来、このような問題を解決するため、磁性キャ
リヤ表面の樹脂コート量を少なくしてその低抵抗化を図
りトナーの帯電量を下げることが考えられている。(Problems to be Solved by the Invention) By the way, when forming a single layer, titanium oxide and chromatic pigments used in white toners and chromatic toners have lower electrical resistance (conductivity) than black pigments such as carbon. If the toner (the opposite of the It has been considered to reduce the amount of resin coating on the carrier surface to lower its resistance and thereby reduce the amount of charge on the toner.
しかしながら、従来の磁性キャリヤはアクリル樹脂がコ
ートされており、低抵抗化を図るために樹脂コート量を
0.01%未満の薄層とすると、キャリヤコアの表面の
被覆保護が十分にされず、キャリヤコアの酸化等により
トナーが汚染される虞がある。特に、白色トナーを用い
た現像剤の場合には、得られる画像が黄色味を帯び、白
色度の乏しいものとなってしまう。However, conventional magnetic carriers are coated with acrylic resin, and if the resin coating amount is less than 0.01% in order to lower the resistance, the surface of the carrier core will not be sufficiently protected. There is a risk that the toner may be contaminated due to oxidation of the carrier core. In particular, in the case of a developer using white toner, the resulting image has a yellowish tinge and has poor whiteness.
また、a性キャリヤの抵抗が低く、 トナーの抵抗が高
い現像剤では、トナー濃度(T/D)(現像剤中のトナ
ー重量分率)に対する現像剤の抵抗値の変化が大となり
、このため、T/D値が若干下がったときでも画像に白
ヌケが見られる。しかも上記のような白ヌケを改良する
ためにキャリヤの粒径を大にすることが考えられるが、
これが過ぎると画質が悪くなってトナーのW4etも多
くなる。また一方、キャリヤの粒径を小とし過ぎると。In addition, in a developer where the resistance of the a-type carrier is low and the resistance of the toner is high, the resistance value of the developer changes greatly with respect to the toner concentration (T/D) (toner weight fraction in the developer). , white spots can be seen in the image even when the T/D value has decreased slightly. Moreover, it is conceivable to increase the particle size of the carrier in order to improve the white spots mentioned above.
If this is exceeded, the image quality will deteriorate and the amount of toner W4et will increase. On the other hand, if the particle size of the carrier is too small.
磁性キャリヤの低抵抗化と相まってホタルやキャリヤ引
きを誘発する不具合が生じてくる。Coupled with the reduction in the resistance of magnetic carriers, problems that induce fireflies and carrier attraction occur.
また、近年、電子写真用感光体として、加工性がよ<I
llココスト面で有利であると共に、機能設計の自由度
が大きな有機感光体が使用されている。このような有機
感光体には負帯電形式のものと正帯電形式のものがある
が、負帯電形式のものは複写環境の汚染を誘発し、感光
体をすぐに劣化させることから好ましくなく、主に正帯
電有機感光体(OPC)の使用が細待されている。In addition, in recent years, it has been used as a photoreceptor for electrophotography because it has good processability.
Organic photoreceptors are used, which are advantageous in terms of cost and have a large degree of freedom in functional design. There are two types of organic photoreceptors: negatively charged types and positively charged types.Negatively charged types are undesirable because they cause contamination of the copying environment and quickly deteriorate the photoreceptor. The use of positively charged organic photoconductors (OPC) is eagerly awaited.
しかしながら、このような正帯電有機感光体は残留電位
が従来のSs系悪感光体比較して大きくなる傾向にあり
、正帯電有機感光体を使用する場合にはバイアス電位を
250V以上で使用しなければならない、バイアス電位
の上昇は磁性キャリヤと現像スリーブとの荷電的反発を
高め、キャリヤ引きを発生しやすくする。従って、正帯
電有機感光体と白色トナーや有彩色トナーを用いた画像
形成に於いては、キャリヤ引きと画質の改善が問題とな
っている。However, the residual potential of such positively charged organic photoreceptors tends to be larger than that of conventional Ss-based negative photoreceptors, and when using positively charged organic photoreceptors, the bias potential must be 250 V or higher. An increase in the bias potential increases charge repulsion between the magnetic carrier and the developing sleeve, making carrier attraction more likely to occur. Therefore, in image formation using a positively charged organic photoreceptor and white toner or chromatic toner, there are problems in carrier attraction and improvement in image quality.
更に、バイアス電位の上昇に伴うW*の品質低下を改善
するため、前述したno−a間を狭めた場合には、現像
剤にストレスがかかり、キャリヤ引きを発生しやすくす
る。Furthermore, in order to improve the quality deterioration of W* caused by an increase in the bias potential, if the above-described distance between no and a is narrowed, stress is applied to the developer, making carrier attraction more likely to occur.
よって1本発明の目的は、導電率の低い白色トナーや有
彩色トナーを用いた場合でも、現像剤の帯電量を適正範
囲に安定化でき、高濃度画像の再現性が豊かな現像剤を
提供することにある。Therefore, one object of the present invention is to provide a developer that can stabilize the amount of charge of the developer within an appropriate range even when using white toner or chromatic toner with low conductivity, and has rich reproducibility of high-density images. It's about doing.
本発明の目的はまた、導電率の低い白色トナーや有彩色
トナーを用い、白ヌケ、ホタル、キャリヤ引き等の不具
合の生じない、高濃度画像を得ることのできる現像剤を
提供することにある。Another object of the present invention is to provide a developer that uses white toner or chromatic toner with low conductivity and is capable of producing high-density images without problems such as white spots, fireflies, and carrier drag. .
本発明の目的は更に、鮮明な白色画体が得られる白色現
像剤を提供することにある。A further object of the present invention is to provide a white developer from which clear white images can be obtained.
本発明はまた。正帯電有機感光体に適用することが好ま
しい現像剤を提供することにある。The present invention also includes: It is an object of the present invention to provide a developer that is preferably applied to positively charged organic photoreceptors.
(課題を解決するための手段)
本発明によれば、導電率が3.5 X 10 ” sl
am以下のカラー現像用トナーと、アミン含有シリコン
樹脂が被覆された磁性キャリヤと、から威ることを特徴
とするカラー現像剤が提供される。(Means for Solving the Problems) According to the present invention, the electrical conductivity is 3.5 x 10” sl
There is provided a color developer characterized by comprising a color developing toner having a particle size of less than am and a magnetic carrier coated with an amine-containing silicone resin.
本発明では、 前記トナーの導電率が2.OX 101
0乃至3.OX 10−” 5acsの範囲を満たすも
のであり、且つ磁性キャリヤの電流値が0.5乃至5μ
Aであることを特徴とすることができる。In the present invention, the conductivity of the toner is 2. OX101
0 to 3. satisfies the range of OX 10-” 5acs, and the current value of the magnetic carrier is 0.5 to 5μ
A.
本発明はまた、前記アミン含有シリコン樹脂が被覆され
たキャリヤの樹脂の被覆量がキャリヤコア材に対して0
.01乃至0.5%であることを特徴とすることができ
る。The present invention also provides that the amount of resin coating of the carrier coated with the amine-containing silicone resin is 0 with respect to the carrier core material.
.. 01 to 0.5%.
本発明では更に、前記キャリヤの重量平均粒径の50%
径 D5゜が70乃至90μmの範囲を満たすことを特
徴とすることができる。In the present invention, 50% of the weight average particle size of the carrier is further provided.
It can be characterized in that the diameter D5° satisfies the range of 70 to 90 μm.
本発明ではまた。前記キャリヤの重量平均粒径の50%
径 D50が80乃至120μmの範囲を満たし、餘担
持体−現像剤担持体間が1■未満で、且つ現像電位差が
500v以下の条件で°用いられることを特徴とするこ
とができ、前記像担持体が正帯電有機感光体とすること
ができる。Also in the present invention. 50% of the weight average particle size of the carrier
It can be characterized in that it is used under the conditions that the diameter D50 satisfies the range of 80 to 120 μm, the distance between the weight carrier and the developer carrier is less than 1 μm, and the development potential difference is 500 V or less, and the image carrier The body can be a positively charged organophotoreceptor.
本発明によれば、トナーが酸化チタンを含有する白色ト
ナーに適用することができる。According to the present invention, the toner can be applied to a white toner containing titanium oxide.
(作用)
本発明は、導電率の低いトナーと、アくン含有シリコン
樹脂をコート樹脂とする磁性キャリヤとを組み合わせて
現像剤としたことにより、そのコートキャリヤに不都合
が生じることがなく、且つその現像剤が極めて良好な高
濃度画像を提供し得るという知見に基づくものである。(Function) The present invention provides a developer by combining a toner with low conductivity and a magnetic carrier whose coat resin is a silicone resin containing aphne, thereby causing no inconvenience to the coat carrier. This is based on the knowledge that the developer can provide extremely good high-density images.
本発明はまた。上記コート樹脂を用いた磁性キャリヤの
粒径を一定の範囲に揃えてgu+iすることにより、キ
ャリヤの低抵抗化によって生じ易くなる現像の際のキャ
リヤ引き、ホタル等の誘発を防止できるという知見にも
基づいている。尚1本明細書において、キャリヤ引きと
は静電潜体がトナーだけでなく、キャリヤによっても現
像されることをいい、ホタルとは静電潜像以外の転写面
にトナーがランダムにスポット状に転写されることをい
う。The present invention also includes: It is also known that by aligning the particle size of the magnetic carrier using the above-mentioned coat resin within a certain range and performing gu+i, it is possible to prevent carrier pull during development and the induction of fireflies, etc., which tend to occur due to the lower resistance of the carrier. Based on. 1 In this specification, carrier attraction refers to the fact that the electrostatic latent material is developed not only by toner but also by carrier, and firefly refers to the fact that toner is randomly spotted on the transfer surface other than the electrostatic latent image. It means to be transcribed.
白色トナーや有彩色トナー等は、その導電率が3−5
X I Q−1o以下、特に3.OX 10−10以下
のものが多くみられる。このようにトナーの導電率が低
くなるのは、 トナー中の着色剤に起因するからである
。前記導電率の範囲内を満たすトナーに於ける着色剤は
有機顔料として多種存在しているが、逆に前記範囲以外
のトナーでは、その着色剤の選択性が乏しいため十分に
好みの色調が得られない、したがって1本発明に於いて
は、 トナー原料として選ぶ場合には全く不自由がなく
、現像剤の色調の輻を広げ豊かにすることができる。The conductivity of white toner and chromatic toner is 3-5.
X I Q-1o or below, especially 3. Many have an OX of 10-10 or less. This low conductivity of toner is due to the colorant in the toner. There are many types of colorants in the form of organic pigments that can be used in toners that satisfy the above range of conductivity, but conversely, in toners that fall outside the above range, the selectivity of the colorant is poor, making it difficult to obtain a desired color tone. Therefore, in the present invention, there is no inconvenience when selecting it as a toner raw material, and it is possible to widen and enrich the color tone of the developer.
しかしながら、このように導電率が3.5×1Q−10
以下、特に3.OX 10−”以下のトナーでは、通常
のキャリヤと組み合わせて使用した場合、トナー帯電量
の増大によって高濃度画像が得難くなる。However, in this way the conductivity is 3.5×1Q-10
Below, especially 3. When a toner of OX 10-'' or less is used in combination with a normal carrier, it becomes difficult to obtain a high-density image due to an increase in the amount of toner charge.
本発明の磁性キャリヤは前述のようにトナー導電率に起
因する帯電量の差を補うため、特定のコート樹脂を使用
してトナー帯電量を適正範囲に安定化させるものである
。As described above, the magnetic carrier of the present invention uses a specific coating resin to stabilize the toner charge amount within an appropriate range in order to compensate for the difference in charge amount caused by the toner conductivity.
即ち、本発明の磁性キャリヤはコート樹脂にア且ン含有
シリコンを用いることによって、コート量を少なくする
ことなく適正トナー帯電量に調整できるものである。That is, in the magnetic carrier of the present invention, by using arn-containing silicon as the coating resin, the amount of toner charge can be adjusted to an appropriate amount without reducing the amount of coating.
第2図に示すように従来のアクリル樹脂コートした磁性
キャリヤでは、そのコート量はせいぜいで0.05%以
下でしか用いることができなかったのに対して、アミン
含有シリコン樹脂の磁性キャリヤでは0.1%までコー
ト量を増量しても帯電量に問題が生じないことが理解さ
れる。したがって、本発明のように、アミン含有シリコ
ンを磁性キャリヤのコート樹脂にした場合には、磁性キ
ャリヤの帯電量を下げ、且つ十分な保護コート層を形成
し得るものである。この樹脂の変更使用による磁性キャ
リヤの帯電量の減少は、トナー帯電量の増加を抑制し、
且つコート量の増加を可能にするものである。As shown in Figure 2, with conventional magnetic carriers coated with acrylic resin, the amount of coating could be used at most 0.05% or less, whereas with magnetic carriers made of amine-containing silicone resin, the amount of coating could be no more than 0.05%. It is understood that even if the coating amount is increased to .1%, no problem arises in the amount of charge. Therefore, when amine-containing silicon is used as the coating resin for the magnetic carrier as in the present invention, the amount of charge on the magnetic carrier can be reduced and a sufficient protective coating layer can be formed. The reduction in the amount of charge on the magnetic carrier due to the changed use of this resin suppresses the increase in the amount of charge on the toner,
Moreover, it is possible to increase the amount of coating.
また、磁性キャリヤの電流値は、キャリヤ材と樹脂コー
ト量と密接に関係しており、m性キャリヤの電流値は0
.1乃至70μAの範囲を満たすように調整することが
望ましい、特に、 Se系感光体を用いる場合は0.
5乃至3μAの範囲がよく、正帯電有機感光体を用いる
場合は30乃至40μAの範囲を満たすものがよい、こ
のように組み合わせた1!14IA剤に於いて得られる
画像は白ヌケのような濃度低下といったものがなく、優
れた高濃度画像が得られる0本明細書において、電流値
とはキャリヤが現像スリーブ上で磁気ブラシを形威し、
且つ移動している状態で200Vの直流電源に接続した
ときの電流値を意味する。尚、白ヌケとは。Furthermore, the current value of the magnetic carrier is closely related to the carrier material and the amount of resin coating, and the current value of the m-type carrier is 0.
.. It is desirable to adjust it so that it satisfies the range of 1 to 70 μA, especially when using a Se-based photoreceptor.
The range of 5 to 3 μA is good, and if a positively charged organic photoreceptor is used, the range of 30 to 40 μA is good.The image obtained with the 1!14 IA agent combined in this way has a density like a white spot. Excellent high-density images can be obtained without any deterioration. In this specification, the current value refers to the current value when the carrier forms a magnetic brush on the developing sleeve.
It also means the current value when connected to a 200V DC power supply while moving. By the way, what is white nuke?
特に潜体のベタ部において、キャリヤがドラム等に付着
してトナーの転写がしない部分をいう。Particularly in the solid portion of the latent material, it refers to the portion where the carrier adheres to the drum or the like and the toner is not transferred.
本発明に於いて、キャリヤの粒径は重量平均粒径の50
%径D5゜が70乃至120 p m、 特にSe系
感光体を使用する際は70乃至90μm、正帯電有機感
光体を使用する際は80乃至120μmのvanを満た
すようにキャリヤの粒径を揃え、前記コート樹脂と組み
合わせて実施することがよい。In the present invention, the particle size of the carrier is 50% of the weight average particle size.
Adjust the particle size of the carrier so that the % diameter D5゜ satisfies the van of 70 to 120 pm, especially 70 to 90 μm when using a Se-based photoreceptor, and 80 to 120 μm when using a positively charged organic photoreceptor. , it is preferable to carry out in combination with the above-mentioned coating resin.
前記範囲内にキャリヤの粒径を揃えた場合にはホタルや
キャリヤ引きが生じ難くなる。即ち、磁性キャリヤの粒
径が前記範囲を下回ると、比較的粒径の小さいキャリヤ
が低抵抗化と相まってホタルやキャリヤ引き等を誘発す
る。一方1粒径が前記IIRHを上回ると、 トナーの
消11Jiが大となる。When the particle size of the carrier is made uniform within the above range, fireflies and carrier attraction are less likely to occur. That is, when the particle size of the magnetic carrier falls below the above range, the relatively small particle size of the carrier causes fireflies, carrier attraction, etc. in combination with a low resistance. On the other hand, if the particle size exceeds the above-mentioned IIRH, the extinction 11Ji of the toner becomes large.
前記キャリヤの粒径の重量平均粒径の50%径D50と
は1重量の小さい粒径のキャリヤを順次カウントしてい
き、この量が全体の50%に達したときに、そのときの
キャリヤの中心粒径の値をいい、カウント方法としては
所定のメツシュの篩にかけて行うことができる。The 50% diameter D50 of the weight average particle size of the carrier particles is defined as the diameter D50 of carriers at which one weight of carriers with a small particle size is sequentially counted and when this amount reaches 50% of the total. It refers to the value of the central particle diameter, and counting can be carried out by passing it through a predetermined mesh sieve.
また1本発明の現像剤はバイアス電位250 V。Further, the developer of the present invention has a bias potential of 250V.
特に280V以上で用いることができる。バイアス電位
を上げることは、感光体の残留電位の影響を少な、くす
ることができる、即ち残留電位が少なくとも150V!
1度の高電位であっても、その感光体はキャリヤ引きを
起こすことなく優れた画質を提供することができる。こ
の場合、キャリヤの粒径は80μm乃至120μmとす
るのがよい。In particular, it can be used at 280V or higher. Increasing the bias potential can reduce or eliminate the influence of the residual potential of the photoreceptor, ie, the residual potential is at least 150V!
Even at one high potential, the photoreceptor can provide excellent image quality without carrier attraction. In this case, the particle size of the carrier is preferably 80 μm to 120 μm.
第3図は従来のキャリヤと本発明のキャリヤとを用いた
現像剤のキャリヤ引き状態とバイアス電位の関係線図で
ある1本発明のキャリヤ粒子群は前記範囲の粒径に揃え
られ、250メツシユ以下のキャリヤが8重量%以下と
なっている。 3113図に示すように従来の現像剤
は、キャリヤ引きがバイアス電位の増加に応じて増大し
ている。これは磁性キャリヤが現像スリーブとの荷電的
反発を徐々に高めるため、キャリヤが感光体に移行し易
くなることが理解される。しかし、本発明の現像剤は磁
性キャリヤの粒径を前記範囲を満たすようにnwiする
ことにより、バイアス電位が増加してもキャリヤ引きが
著しく抑えられている。FIG. 3 is a diagram showing the relationship between the carrier attraction state and the bias potential of the developer using a conventional carrier and the carrier of the present invention. The following carriers are 8% by weight or less. As shown in Figure 3113, in the conventional developer, carrier attraction increases as the bias potential increases. It is understood that this is because the magnetic carrier gradually increases the charge repulsion with the developing sleeve, making it easier for the carrier to transfer to the photoreceptor. However, in the developer of the present invention, by controlling the particle size of the magnetic carrier to satisfy the above range, carrier attraction is significantly suppressed even when the bias potential increases.
また、このような残留電位の高い感光体として、正帯電
有機感光体(o p c)等があげられるが、この正帯
電有機感光体は本発明の現像剤が好適に用いられる条件
を備えているものである。また、バイアス電位の上昇は
、その電位の表面電位との差で与えられる現像電位差を
低下させ、場合によっては低電位現像が強いられる。こ
のような低電位現像では画像濃度を悪くする。しかしな
がら、前述のDo−s巾が1.2m未満、特に1.0■
未満の現像条件とすれば、階調性、W像濃度とも優れた
ものに維持され、キャリヤ引きも生じない、このことか
らも本発明の現像剤は正帯電有機感光体に適用すること
が可能である。In addition, examples of such photoreceptors with a high residual potential include positively charged organic photoreceptors (OPC), which positively charged organic photoreceptors are provided with conditions for suitably using the developer of the present invention. It is something that exists. Further, an increase in the bias potential lowers the development potential difference given by the difference between this potential and the surface potential, and in some cases, low potential development is forced. Such low potential development deteriorates image density. However, the above-mentioned Do-s width is less than 1.2 m, especially 1.0
Under developing conditions below, excellent gradation and W image density are maintained, and carrier attraction does not occur.For this reason, the developer of the present invention can be applied to positively charged organic photoreceptors. It is.
(発明の好ましい実施態様)
以下、本発明に係る現像剤の好ましい実施態様を説明す
る。(Preferred Embodiments of the Invention) Preferred embodiments of the developer according to the present invention will be described below.
本発明の現像剤は磁性キャリヤとトナーとの二成分系現
像剤であり、磁性キャリヤ、 トナー、及び現像剤につ
いて順次解説する。The developer of the present invention is a two-component developer consisting of a magnetic carrier and a toner, and the magnetic carrier, toner, and developer will be explained in turn.
匙艷土工亙ユ
本発明においては、磁性キャリヤとして、前述したよう
にアミン含有シリコン樹脂をコーテングしたフェライト
粒子等の使用が好適で、粒径分布が前述した範囲内にあ
ることが望ましい。In the present invention, as the magnetic carrier, it is preferable to use ferrite particles coated with an amine-containing silicone resin as described above, and it is desirable that the particle size distribution is within the range described above.
即ち、アえン含有シリコンとしては、アミンを含有して
いるものであり、その含有量は0.1乃至10重量%、
特に0.1乃至5重量%のI[Nを満たすことが望まし
く、アクリル系シリコン等のような炭化水素だけのもの
やハロゲン元素等のみを含有したものは含まれない、ま
たフェライト粒子に対するコート量は0.01乃至1.
0%、特に0.02乃至0.7%の範囲を満たすものが
望ましく、樹脂コート量がこの範囲より少ない場合には
フェライト粒子表面の錆等を充分に防止できず、また前
記範囲より多い場合には磁性キャリヤの帯電量が増大し
好ましくない。That is, the amine-containing silicon contains amine, and the content thereof is 0.1 to 10% by weight.
In particular, it is desirable to satisfy 0.1 to 5% by weight of I[N, and do not include those containing only hydrocarbons such as acrylic silicon, or those containing only halogen elements, and the amount of coating on ferrite particles. is 0.01 to 1.
It is desirable that the amount of resin coating satisfies the range of 0%, especially 0.02 to 0.7%.If the resin coating amount is less than this range, rust etc. on the surface of the ferrite particles cannot be sufficiently prevented, and if it is more than the above range. This is undesirable because the amount of charge on the magnetic carrier increases.
具体的なアミン含有シリコンとしては、アルキルアミン
系、芳香翼アζン系シリコンが好ましく。As specific amine-containing silicones, alkylamine-based and aromatic winged amine-based silicones are preferred.
特にベンジルアミン系シリコンのような芳香属系アミン
が望ましい。In particular, aromatic amines such as benzylamine silicone are preferred.
フェライトとして、具体的なものは例えば酸化#亜鉛(
ZnFezOn)、Il化峡イツトリウム(Y3Fas
O+z)。Specific examples of ferrite include #zinc oxide (
ZnFezOn), Y3Fas
O+z).
酸化鉄カドミニウム(CdFe、On) 、 l[化畝
ガドリニウム(GdFe20.2)、酸化銃鉛(PdF
es20+*) 、 II化麩ニッケル(NiFe20
t3、酸化鉄ネオジウム(NdFeOs)、酸化麩バリ
ウム(BaFelzOss) 、 lk化銑鉄マグネシ
ウムMgFe2O4) 、 liI化畝マンガン(Mn
Fe204) 、II化銑鉄ランタンLaFeOs)等
の1種或いは2種以上からなる組成の焼結フェライト粒
子が使用されており。Cadmium iron oxide (CdFe, On), gadolinium (GdFe20.2), lead oxide (PdF
es20+*), II-based wheat nickel (NiFe20
t3, neodymium iron oxide (NdFeOs), barium oxide (BaFelzOss), pig iron magnesium MgFe2O4), liI manganese (Mn)
Sintered ferrite particles having a composition consisting of one or more of Fe204), lanthanum II pig iron oxide (LaFeOs), etc. are used.
特にCu、 Zn、 Hl、 Mn、 及びNiから
戒る群より選ばれた金属成分の少なくとも1種、好適に
は2種以上を含有するソフトフェライト、例えば綱−亜
鉛−マグネシウムフェライト等が使用できる。In particular, soft ferrite containing at least one, preferably two or more metal components selected from the group consisting of Cu, Zn, Hl, Mn, and Ni, such as steel-zinc-magnesium ferrite, can be used.
本発明において、上記樹脂コートした磁性キャリヤ粒子
は球状のものが流動性の点から望ましく、そのキャリヤ
粒子群においては重量平均中心粒径の50%径り、。が
前述の範囲を満たすことが重要である。このような範囲
の粒径の調整はそれ自体公知の方法で行うことができ、
フェライトの焼結時に調整してもよく、また、コート樹
脂を施した後に調整することができる。このような範囲
にキャリヤ粒子群を揃えることは 前記したように白ヌ
ケ等の不具合やトナーの転写率の向上を図ることができ
る。In the present invention, the resin-coated magnetic carrier particles are preferably spherical from the viewpoint of fluidity, and in the carrier particle group, the diameter is 50% of the weight average median particle diameter. It is important that the value satisfies the aforementioned range. Adjustment of the particle size in such a range can be performed by a method known per se,
The adjustment may be made during sintering of the ferrite, or after the coating resin is applied. Arranging the carrier particles in such a range can prevent problems such as white spots and improve the toner transfer rate, as described above.
更に、キャリヤ粒子群を前述の粒径に揃えると共に1重
量平均中心粒怪の25%径D25と75%径I)tsと
の差がO乃至20μmの範囲を満たすように揃えた場合
は1粒径分布が更にシャープとなり、後述する。−5巾
を1m未満から更に短縮してもキャリヤ引きがない状態
となる。*た。バイアス電位の高い状態であってもキャ
リヤ引きが防止される。更に、このような粒度分布の磁
性キャリヤでは1画慟濃度の向上がみられ、キャリヤ粒
度分布のシャープ化に基づく粒径の底上げは、像担持体
と現像剤担持体がドラム形式の場合において、トルクを
軽減し、 ドラム周擦力を軽減する。Furthermore, if the carrier particles are arranged to have the above-mentioned particle size and the difference between the 25% diameter D25 and the 75% diameter I) ts of the 1 weight average center grain is within the range of 0 to 20 μm, then 1 grain. The diameter distribution becomes even sharper, which will be described later. -5 Even if the width is further shortened from less than 1 m, there will be no carrier pull. *Ta. Carrier attraction is prevented even when the bias potential is high. Furthermore, with a magnetic carrier having such a particle size distribution, an improvement in the per-image density is observed, and the increase in particle size based on the sharpening of the carrier particle size distribution is achieved when the image carrier and developer carrier are in the form of a drum. Reduces torque and drum circumferential friction.
更に、キャリヤ引きを充分に防止するものとして、25
0メツシユ以下の微小粒径キャリヤの排除が望ましい1
粒度分布で250メツシユ以下のキャリヤ量は8重量%
以下、特番こ5重量%以下の範囲を満たすものが望まし
く、このような範囲を満たす現体剤では、バイアス電位
の高い状態であってもキャリヤ引きを充分に防止し、鮪
述以外の効果としてカブリ等を少なくする。Furthermore, as a material that sufficiently prevents carrier pull, 25
It is desirable to eliminate carriers with a microparticle size of 0 mesh or less1
The amount of carrier with a particle size distribution of 250 mesh or less is 8% by weight.
Below, it is desirable to use a developer that satisfies the range of 5% by weight or less.A developer that satisfies this range sufficiently prevents carrier attraction even in a state where the bias potential is high, and has other effects other than those mentioned above. Reduce fog etc.
磁性キャリヤの飽和磁化は50乃至7 Q emu/z
の範囲を満たすものが用いられ、特に55乃至65e鵬
u/gの範囲のものは従来の現像剤用キャリヤの飽和磁
化より低く抑えられ、この磁性キャリヤは従来のキャリ
ヤと比較して磁気ブラシに於ける穂のソフト化を促し、
穂のソフト化はドラムストレスを減少させるものである
。特にDo−g巾を1.21未満としたとき、更には1
.0 mm未満としたときに望ましい、また1本発明に
用いられるキャリヤの流動波は15乃至35 sec/
50 g、特に20乃至30sec150gの範囲を
満たすものが望ましい。The saturation magnetization of the magnetic carrier is 50 to 7 Q emu/z
In particular, those in the range of 55 to 65 u/g have a saturation magnetization lower than that of conventional developer carriers, and this magnetic carrier is more sensitive to magnetic brushes than conventional carriers. Promote the softening of the ears,
Softening the ears reduces drum stress. Especially when the dog width is less than 1.21,
.. The flow wave of the carrier used in the present invention is preferably less than 0 mm, and the flow wave of the carrier is 15 to 35 sec/
50 g, especially one that satisfies the range of 150 g for 20 to 30 seconds.
トナー
本発明に用いるトナーは、定着用樹脂媒質中に白色や有
彩色の着色剤及び電荷制御剤或いは更にそれ自体周知の
トナー用配合剤を配合したものであり、トナーの導電率
は3.5 X 10−” s/an以下。Toner The toner used in the present invention is a fixing resin medium containing a white or chromatic colorant, a charge control agent, or a well-known toner compound, and has an electrical conductivity of 3.5. X 10-” s/an or less.
特に3.OX I Q ” s/m以下、 2.OX
10−” s10以上の晩囲を満たすものである。ト
ナー用の定着用樹脂媒質、着色剤、電荷制御剤及びその
他のトナー用配合剤については、上記特性を備えた範囲
で適宜に組み合わせて使用される。Especially 3. OX IQ ” s/m or less, 2.OX
The fixing resin medium, colorant, charge control agent, and other compounding agents for toner may be used in appropriate combinations within the range that has the above characteristics. be done.
定着用樹脂媒体としては、スチレン系樹脂、アクリル系
樹脂或いはスチレン−アクリル系樹脂、ポリエステル樹
脂、ポリウレタン樹脂、シリコン樹脂、ボリアミド、変
性ロジン等が使用される。As the fixing resin medium, styrene resin, acrylic resin, styrene-acrylic resin, polyester resin, polyurethane resin, silicone resin, polyamide, modified rosin, etc. are used.
スチレン−アクリル系共重合体樹脂は、樹脂媒質として
好適なものの一つであり、スチレン系単量体(A)とア
クリル系単量体(B)とは、A:B=50: 50乃
至90:10、特に60:40乃至85:15の範囲と
するのがよい、また、用いる樹脂は、一般にO乃至25
の酸価を有するのが好ましい、また、定着性の見地から
50乃至65℃のガラス転移温度(Tg)を有するのが
よい。Styrene-acrylic copolymer resin is one of the suitable resin media, and the styrene monomer (A) and acrylic monomer (B) have a ratio of A:B=50:50 to 90. :10, especially preferably in the range of 60:40 to 85:15, and the resin used is generally O to 25
In addition, from the viewpoint of fixing properties, it is preferable to have a glass transition temperature (Tg) of 50 to 65°C.
樹脂中に含有させる着色剤としては、この分野で従来よ
り使用されている公知のものであるが、これ等の導電率
は前記範囲のものが使用される。The coloring agent to be contained in the resin is a known coloring agent that has been conventionally used in this field, and those having electrical conductivity within the above range are used.
着色剤はホワイト系、シアン系、マゼンタ系、イエロー
系顔料に大きく大別することまた、これらの着色剤は前
記結着樹脂に対して、1重量%乃至20重量%の範囲で
含有させることが望ましい。Coloring agents are broadly classified into white pigments, cyan pigments, magenta pigments, and yellow pigments.Furthermore, these colorants may be contained in a range of 1% to 20% by weight based on the binder resin. desirable.
次に、具体的な着色剤について示す、具体的な着色剤と
しては、
例えば、マゼンタ系着色剤としては、C,1,ピグメン
トレッド81. C,1,ピグメントレッド122、
C,1,ピグメントレッド57、C,1,ソルベントレ
ッド49. C,1,ソルベントレッド19、C,1
,ソルベントレッド52、C,1,ベシック(Basi
c)レッド10、C,1,ディスバーズ(Disper
se)レッド15等が挙げられ、シアン系着色剤として
は、 C,1,ピグメントブルー15. C,1,
ピグメントブルー16. C,1,ソルベントブルー
25、C,1,ソルベントブルー55゜C,!、ソルベ
ントブルーフ0、C,1,ダイレクトブルー86.
C,1,ダイレクトブルー25等が挙げられ。Next, as specific colorants, for example, as a magenta colorant, C, 1, Pigment Red 81. C, 1, Pigment Red 122,
C,1, Pigment Red 57, C,1, Solvent Red 49. C,1, Solvent Red 19, C,1
,Solvent Red 52,C,1,Basi
c) Red 10, C, 1, Disper
se) Red 15, etc., and cyan colorants include C,1, Pigment Blue 15. C,1,
Pigment Blue 16. C, 1, Solvent Blue 25, C, 1, Solvent Blue 55°C,! , Solvent Blue 0, C, 1, Direct Blue 86.
Examples include C, 1, Direct Blue 25, etc.
イエロー系着色剤としてはC,1,ピグメントイエロー
17. C,1,ピグメントイエロー12.C,1,
ピグメントイエロー1、C,1,ピグメントイエロー9
7゜C,1,ピグメントイエロー138. C,1,
ピグメントイエロー12.c、1.ピグメントイエロー
73、C,1,ピグメントイエロー13、C,1,ソル
ベントイエロー29、C,1,ソルベントイエロー16
2゜C1・工、ソルベントイエロー93等が挙げられ、
また白色顔料としては、亜鉛華 m化チタン、アンチモ
ン白、硫化亜鉛等であり、特に酸化チタン等が挙げられ
る。Yellow colorants include C.1, Pigment Yellow 17. C, 1, Pigment Yellow 12. C,1,
Pigment Yellow 1, C, 1, Pigment Yellow 9
7°C, 1, Pigment Yellow 138. C,1,
Pigment Yellow 12. c.1. Pigment Yellow 73, C,1, Pigment Yellow 13, C,1, Solvent Yellow 29, C,1, Solvent Yellow 16
Examples include 2゜C1・Work, Solvent Yellow 93, etc.
Examples of the white pigment include zinc titanium oxide, antimony white, and zinc sulfide, particularly titanium oxide.
次に電荷制御剤としてはそれ自体公知の任意の電荷制御
剤、例えばニグロシンベース(CI 50415)。The charge control agent can then be any charge control agent known per se, such as nigrosine base (CI 50415).
オイルブラック(CI 26150)、 スピロンブ
ラック等の油溶性染料、含金属アゾ染料、ナフテン酸金
属塩、アルキリルサリチル酸の金属塩、脂肪酸や石鹸、
樹脂酸石鹸等が使用される。Oil black (CI 26150), oil-soluble dyes such as spirone black, metal-containing azo dyes, naphthenic acid metal salts, alkylsalicylic acid metal salts, fatty acids and soaps,
Resin acid soap etc. are used.
トナー粒子の粒径は、コールタ−カウンターで測定した
粒径は体積基準メジアン系で8乃至14μm、特に10
乃至12μmの範囲にあるのがよく、また粒子形状は溶
融混線・粉砕法で製造された不定形のものでも、また分
散乃至闇濁重合法で製造された球状のものでもよい、ま
た、 トナーの表面には、疎水性シリカ微粒子や樹脂粉
等のそれ自体公知表面処理剤をまぶして、その流動性を
向上させてもよい。The particle size of the toner particles is 8 to 14 μm on a volume basis, especially 10 μm as measured by a Coulter counter.
It is preferable that the particle size is in the range of 12 μm to 12 μm, and the particle shape may be an amorphous particle produced by a melt mixing/pulverization method, or a spherical particle produced by a dispersion or cloud polymerization method. The surface may be sprinkled with a surface treatment agent known per se such as hydrophobic silica particles or resin powder to improve its fluidity.
髪皇1
現像剤は前述の磁性キャリヤとトナーとが通常99:
l乃至90:10、特に98: 2乃至95:5の重量
比で混合して使用するのが望ましい。Hair Emperor 1 The developer usually contains the above-mentioned magnetic carrier and toner in a ratio of 99:
It is desirable to mix and use them at a weight ratio of 1 to 90:10, particularly 98:2 to 95:5.
また、現像剤の初期帯電量は、ブローオフ法で測定して
5乃至25μc / g、特に10乃至20μc /
gの範囲を満たすことが望ましい。現像剤のゆるみ見掛
比重としては1.7乃至2.1(g/c朧き)、特に1
.8乃至2.0 (z/cm’)の範囲を満たすものが
本発明の目的に好ましい。In addition, the initial charge amount of the developer is 5 to 25 μc/g, especially 10 to 20 μc/g, as measured by the blow-off method.
It is desirable to satisfy the range of g. The loose apparent specific gravity of the developer is 1.7 to 2.1 (g/c hazy), especially 1
.. Those satisfying the range of 8 to 2.0 (z/cm') are preferred for the purpose of the present invention.
本発明の現像剤はこの分野における通常の現像条件で行
われるが、特に画*a度を向上させたい場合には、像担
持体−現像剤担持体距離Do−aが1.2m未満で、且
つ現像電位差が500V以下の条件のもとで用いること
が望ましい、使用現像機構の像担持体及び現像剤担持体
は、平面的な形式或いは第1図に示されるドラム形式で
あってよく。The developer of the present invention is used under the usual developing conditions in this field, but when it is particularly desired to improve the image *a degree, the image carrier-developer carrier distance Do-a is less than 1.2 m. The image carrier and developer carrier of the developing mechanism to be used, which is preferably used under the condition that the developing potential difference is 500 V or less, may be of a flat type or a drum type as shown in FIG.
DD−Bが前記範囲を満たすことが望ましい。It is desirable that DD-B satisfies the above range.
D o−s巾が1.2m未満、特に1m未満の現像条件
にある現像剤は、低電位現像においても#間伐。Developers under development conditions where the D o-s width is less than 1.2 m, especially less than 1 m, are #thinned even in low potential development.
カラー画像濃度の優れたものを提供し得るものであり、
前記キャリヤの要件を加味したものはキャリヤ引き等も
生じさせない、更に、 Do−a巾の縮小に応じて穂
切り中を0.5乃至1.5 wIL、特に0.7乃至1
.2mの範囲に設けることが望ましい。It can provide excellent color image density,
If the above carrier requirements are taken into account, carrier pull etc. will not occur, and furthermore, depending on the reduction of the Do-a width, the wIL during ear cutting will be 0.5 to 1.5, especially 0.7 to 1.
.. It is desirable to provide it within a range of 2 m.
また、本発明の現像剤は現像電位差を500V、特に4
80v以下の条件とすると、感光体ドラムの表面電位が
750乃至850Vに印加される場合には、バイアス電
位を250乃至350Vに印加した感光体ドラム等の使
用が可能となる。このようなバイアス電位の上昇におい
て、感光体ドラムはその残留電位が150V以上程度、
特に200V程度の場合でも用いることができる。Further, the developer of the present invention has a development potential difference of 500V, especially 4
Under the condition of 80V or less, if the surface potential of the photoreceptor drum is applied to 750 to 850V, it becomes possible to use a photoreceptor drum or the like to which a bias potential of 250 to 350V is applied. In such a rise in bias potential, the residual potential of the photoreceptor drum is approximately 150V or more,
In particular, it can be used even when the voltage is about 200V.
感光体としては、従来の電子写真法に使用されている感
光体、例えばセレン感光体、非晶質シリコン感光体、欧
化亜鉛感光体、セレン化カドミニウム感光体、硫化カド
粟ニウム感光体等を用いることができるが4本発明では
現像剤をセレン系膿光体及び正帯電有機感光体(opc
)に用いることが望ましい、正帯電有機感光体は電荷発
生材料と電荷輸送材料とが主に一層中に混在されている
ため、その−層中で電子と正孔を移動し、どちらかのも
のがトラップとなり、残留電位が大きくなる傾向にある
。このような感光体はバイアス電位を少なくとも250
V以上、場合によっては280V以上で使用しなければ
ならない0本発明の現像剤はこのようなバイアス電位に
おいても優れた画像を提供し、且つキャリヤ引きを生じ
させない。As the photoreceptor, a photoreceptor used in conventional electrophotography, such as a selenium photoreceptor, an amorphous silicon photoreceptor, a zinc chloride photoreceptor, a cadmium selenide photoreceptor, a cadmium sulfide photoreceptor, etc. is used. However, in the present invention, the developer is a selenium-based photoreceptor and a positively charged organic photoreceptor (OPC).
The positively charged organic photoreceptor, which is preferably used for becomes a trap, and the residual potential tends to increase. Such a photoreceptor has a bias potential of at least 250
The developer of the present invention provides excellent images even at such bias potentials and does not cause carrier attraction.
具体的な正帯電有機感光体としては1周知の電荷発生材
および電荷輸送材を組み合わせた感光体を用いることが
でき、特に、先に提案した特WW@62−27158号
公報、の有機感光体等が望ましい。As a specific positively charged organic photoreceptor, a photoreceptor in which a well-known charge generating material and a charge transporting material are combined can be used, and in particular, the organic photoreceptor proposed earlier in Japanese Patent Application Publication No. 62-27158 can be used. etc. is desirable.
(発明の効果)
本発明によれば、導電率が3.5 X I Q −”
s/国以下、特に2.OX 10−10乃至3−OX
10−” aI国の範囲を満たすカラートナーを用い、
且つキャリヤの樹脂コートにアミン含有シリコンを用い
たので、磁性キャリヤの被覆に不具合を生じることなく
、高濁度の画像を提供することができる。(Effect of the invention) According to the invention, the electrical conductivity is 3.5
s/country or less, especially 2. OX 10-10 to 3-OX
Using color toner that meets the range of 10-”aI countries,
Furthermore, since amine-containing silicone is used for the resin coating of the carrier, a highly turbid image can be provided without causing any defects in the coating of the magnetic carrier.
また、白色現像剤においては、キャリヤコアの酸化物に
よ°るトナーの汚染が防止され、白色度の高い鮮明な白
色画像を提供することができる。In addition, in the case of a white developer, contamination of the toner by oxides of the carrier core is prevented, and a clear white image with high whiteness can be provided.
更にキャリヤの粒径を選定することにより、白ヌケやキ
ャリヤ引きなどの現像の際の不都合を解消することがで
きると共に、l!像条件の変更を行うことにより1本発
明は更に画像濃度を向上させることができる。しかも、
最近頻用される傾向にある有機感光体用の現像剤、特に
正帯電型の感光体用に現像剤として十分に適用すること
ができる。Furthermore, by selecting the particle size of the carrier, it is possible to eliminate inconveniences during development such as white spots and carrier drag, and also to improve l! By changing the image conditions, the present invention can further improve the image density. Moreover,
It can be satisfactorily applied as a developer for organic photoreceptors, which have recently been frequently used, particularly for positively charged type photoreceptors.
(実施例)
以下、実施例及び比較例を示す、尚、本発明は実施例の
範囲に限るものではない。(Example) Examples and comparative examples will be shown below, but the present invention is not limited to the scope of the examples.
現像剤の成分及び現像条件をつ「の様に設定し東ゑ
磁性キャリヤは球状のアミン含有シリコンコートフェラ
イトキャリヤ、アクリル系重合体を用い、その物性を表
1に示した。The components of the developer and the developing conditions were set as follows. The Toe magnetic carrier was a spherical amine-containing silicone coated ferrite carrier and an acrylic polymer, and its physical properties are shown in Table 1.
トナーは粒径、顔料成分、導電率等の知られているもの
を使用した。その物性を表1に示した。A toner with known particle size, pigment components, electrical conductivity, etc. was used. Its physical properties are shown in Table 1.
現像剤はトナーとキャリヤを重量比4.5: 95.5
で混合し、基本物性を表1に示した。The developer has a weight ratio of toner and carrier of 4.5:95.5.
The basic physical properties are shown in Table 1.
現像条件
りゎ−6巾、穂切り巾、現像電位差、バイアス電位及び
感光体を表1に示した。Table 1 shows the developing conditions: width-6 width, cutting width, developing potential difference, bias potential, and photoreceptor.
以上の条件及び成分の現像剤を用いて現像した結果(キ
ャリヤ引き、画像濃度〉を表1に示す。Table 1 shows the results of development (carrier attraction, image density) using the developer with the above conditions and components.
111図は現像機構部の説明図、
112図は樹脂コ
ート量とキャリヤの帯電量との関係線図。
jlI3図
はバイアス電位とキャリヤ引きの関係を示した特性線図
である。FIG. 111 is an explanatory diagram of the developing mechanism section, and FIG. 112 is a diagram showing the relationship between the amount of resin coating and the amount of charge on the carrier. Figure jlI3 is a characteristic diagram showing the relationship between bias potential and carrier attraction.
Claims (7)
のカラー現像用トナーと、アミン含有シリコン樹脂が被
覆された磁性キャリヤと、から成ることを特徴とするカ
ラー現像剤。(1) A color developer comprising a color developing toner having an electrical conductivity of 3.5×10^-^1^0 s/cm or less and a magnetic carrier coated with an amine-containing silicone resin.
乃至3.0×10^−^1^0s/cmの範囲を満たす
ものであり、且つ磁性キャリヤの電流値が0.5乃至5
μAであることを特徴とする請求項第1項記載の現像剤
。(2) The conductivity of the toner is 2.0×10^-^1^0
The current value of the magnetic carrier is 0.5 to 5.
2. The developer according to claim 1, wherein the developer is μA.
ヤの樹脂の被覆量がキャリヤコア材に対して0.01乃
至0.5%であることを特徴とする請求項第1項乃至第
2項記載の現像剤。(3) The coating amount of the carrier coated with the amine-containing silicone resin is 0.01 to 0.5% based on the carrier core material. developer.
0が70乃至90μmの範囲を満たすことを特徴とする
請求項第1項乃至第3項記載の現像剤。(4) 50% diameter D_5_ of the weight average particle diameter of the carrier
4. The developer according to claim 1, wherein 0 satisfies a range of 70 to 90 μm.
0が80乃至120μmの範囲を満たし、像担持体−現
像剤担持体間が1mm未満で、且つ現像電位差が500
V以下の条件で用いられることを特徴とする請求項第1
項乃至第3項記載の現像剤。(5) 50% diameter D_5_ of the weight average particle diameter of the carrier
0 satisfies the range of 80 to 120 μm, the distance between the image carrier and the developer carrier is less than 1 mm, and the development potential difference is 500 μm.
Claim 1 is characterized in that it is used under the conditions of V or less.
The developer according to items 1 to 3.
徴とする請求項第5項記載の現像剤。(6) The developer according to claim 5, wherein the image carrier is a positively charged organic photoreceptor.
あることを特徴とする請求項第1項乃至第6項記載の現
像剤。(7) The developer according to any one of claims 1 to 6, wherein the toner is a white toner containing titanium oxide.
Priority Applications (5)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2049513A JP2648221B2 (en) | 1989-10-09 | 1990-03-02 | Magnetic brush development method using white toner |
DE1990616913 DE69016913T2 (en) | 1989-10-09 | 1990-10-09 | Developer and development process. |
ES90311048T ES2071037T3 (en) | 1989-10-09 | 1990-10-09 | DEVELOPING AGENT AND DEVELOPMENT PROCESS USING SUCH DEVELOPING AGENT. |
EP19900311048 EP0422892B1 (en) | 1989-10-09 | 1990-10-09 | Developer and developing process using said developer |
US07/838,325 US5258253A (en) | 1989-10-09 | 1992-02-20 | Magnetic carrier for electronic reproduction coated with a nitrogen containing silicone resin |
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP1-262243 | 1989-10-09 | ||
JP26224389 | 1989-10-09 | ||
JP2049513A JP2648221B2 (en) | 1989-10-09 | 1990-03-02 | Magnetic brush development method using white toner |
Publications (2)
Publication Number | Publication Date |
---|---|
JPH03200978A true JPH03200978A (en) | 1991-09-02 |
JP2648221B2 JP2648221B2 (en) | 1997-08-27 |
Family
ID=26389909
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP2049513A Expired - Lifetime JP2648221B2 (en) | 1989-10-09 | 1990-03-02 | Magnetic brush development method using white toner |
Country Status (4)
Country | Link |
---|---|
EP (1) | EP0422892B1 (en) |
JP (1) | JP2648221B2 (en) |
DE (1) | DE69016913T2 (en) |
ES (1) | ES2071037T3 (en) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2000187359A (en) * | 1998-12-24 | 2000-07-04 | Kyocera Mita Corp | Electrostatic latent image developing carrier and electrostatic latent image developer |
JP2016184164A (en) * | 2015-03-25 | 2016-10-20 | コニカミノルタ株式会社 | Image forming method, electrostatic charge image developer set, and image forming apparatus |
Families Citing this family (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH11143129A (en) * | 1997-11-11 | 1999-05-28 | Brother Ind Ltd | Dyed toner |
Citations (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS58168056A (en) * | 1982-03-15 | 1983-10-04 | ゼロツクス・コ−ポレ−シヨン | Organoalkoxysilane carrier covering agent |
JPS59105652A (en) * | 1982-12-09 | 1984-06-19 | Konishiroku Photo Ind Co Ltd | Toner for developing electrostatic charge image |
JPS59139056A (en) * | 1983-01-31 | 1984-08-09 | Mita Ind Co Ltd | Magnetic brush developing method |
JPS59228261A (en) * | 1983-06-09 | 1984-12-21 | Fuji Xerox Co Ltd | Two-component type developer for electrophotography |
JPS6159361A (en) * | 1984-08-31 | 1986-03-26 | Mita Ind Co Ltd | Formation of negative and positive image by electrophotography |
JPS62125370A (en) * | 1985-11-27 | 1987-06-06 | Mita Ind Co Ltd | High-speed developing method for amorphous silicon photoconductive layer |
JPS64574A (en) * | 1987-02-26 | 1989-01-05 | Mita Ind Co Ltd | White toner |
Family Cites Families (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5913027B2 (en) * | 1975-11-26 | 1984-03-27 | 株式会社リコー | Fukushimai Fukushiyahouhou |
JPS6350866A (en) * | 1986-08-21 | 1988-03-03 | Minolta Camera Co Ltd | Electrostatic latent image developing carrier |
-
1990
- 1990-03-02 JP JP2049513A patent/JP2648221B2/en not_active Expired - Lifetime
- 1990-10-09 ES ES90311048T patent/ES2071037T3/en not_active Expired - Lifetime
- 1990-10-09 DE DE1990616913 patent/DE69016913T2/en not_active Expired - Fee Related
- 1990-10-09 EP EP19900311048 patent/EP0422892B1/en not_active Expired - Lifetime
Patent Citations (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS58168056A (en) * | 1982-03-15 | 1983-10-04 | ゼロツクス・コ−ポレ−シヨン | Organoalkoxysilane carrier covering agent |
JPS59105652A (en) * | 1982-12-09 | 1984-06-19 | Konishiroku Photo Ind Co Ltd | Toner for developing electrostatic charge image |
JPS59139056A (en) * | 1983-01-31 | 1984-08-09 | Mita Ind Co Ltd | Magnetic brush developing method |
JPS59228261A (en) * | 1983-06-09 | 1984-12-21 | Fuji Xerox Co Ltd | Two-component type developer for electrophotography |
JPS6159361A (en) * | 1984-08-31 | 1986-03-26 | Mita Ind Co Ltd | Formation of negative and positive image by electrophotography |
JPS62125370A (en) * | 1985-11-27 | 1987-06-06 | Mita Ind Co Ltd | High-speed developing method for amorphous silicon photoconductive layer |
JPS64574A (en) * | 1987-02-26 | 1989-01-05 | Mita Ind Co Ltd | White toner |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2000187359A (en) * | 1998-12-24 | 2000-07-04 | Kyocera Mita Corp | Electrostatic latent image developing carrier and electrostatic latent image developer |
JP2016184164A (en) * | 2015-03-25 | 2016-10-20 | コニカミノルタ株式会社 | Image forming method, electrostatic charge image developer set, and image forming apparatus |
US9897935B2 (en) | 2015-03-25 | 2018-02-20 | Konica Minolta, Inc. | Image forming method, electrostatic charge image developer set, and image forming apparatus |
Also Published As
Publication number | Publication date |
---|---|
ES2071037T3 (en) | 1995-06-16 |
EP0422892A3 (en) | 1991-05-29 |
EP0422892A2 (en) | 1991-04-17 |
DE69016913T2 (en) | 1995-06-08 |
JP2648221B2 (en) | 1997-08-27 |
EP0422892B1 (en) | 1995-02-15 |
DE69016913D1 (en) | 1995-03-23 |
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