JPH0329961A - Liquid developer for magnetography - Google Patents
Liquid developer for magnetographyInfo
- Publication number
- JPH0329961A JPH0329961A JP1164576A JP16457689A JPH0329961A JP H0329961 A JPH0329961 A JP H0329961A JP 1164576 A JP1164576 A JP 1164576A JP 16457689 A JP16457689 A JP 16457689A JP H0329961 A JPH0329961 A JP H0329961A
- Authority
- JP
- Japan
- Prior art keywords
- carrier liquid
- magnetic
- magnetography
- solvent
- magnetic toner
- 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.)
- Pending
Links
- 239000007788 liquid Substances 0.000 title claims abstract description 84
- 239000002904 solvent Substances 0.000 claims abstract description 26
- 239000011230 binding agent Substances 0.000 claims abstract description 19
- 239000003086 colorant Substances 0.000 claims abstract description 12
- 239000006249 magnetic particle Substances 0.000 claims abstract description 9
- 239000000696 magnetic material Substances 0.000 claims description 4
- 239000000126 substance Substances 0.000 claims description 2
- 229920000642 polymer Polymers 0.000 abstract description 17
- 239000002270 dispersing agent Substances 0.000 abstract description 16
- 239000006185 dispersion Substances 0.000 abstract description 11
- 238000001704 evaporation Methods 0.000 abstract description 4
- 230000008020 evaporation Effects 0.000 abstract description 4
- 125000002252 acyl group Chemical group 0.000 abstract description 2
- 125000000217 alkyl group Chemical group 0.000 abstract description 2
- 239000000203 mixture Substances 0.000 description 19
- 238000000034 method Methods 0.000 description 7
- 238000004898 kneading Methods 0.000 description 6
- 239000002245 particle Substances 0.000 description 6
- 229920005989 resin Polymers 0.000 description 6
- 239000011347 resin Substances 0.000 description 6
- 239000004094 surface-active agent Substances 0.000 description 6
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 5
- -1 etc. Substances 0.000 description 5
- 229920000620 organic polymer Polymers 0.000 description 5
- 239000000843 powder Substances 0.000 description 4
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 3
- 150000001298 alcohols Chemical class 0.000 description 3
- 229910052799 carbon Inorganic materials 0.000 description 3
- 229920006026 co-polymeric resin Polymers 0.000 description 3
- 239000000975 dye Substances 0.000 description 3
- 239000000945 filler Substances 0.000 description 3
- 238000010438 heat treatment Methods 0.000 description 3
- 238000004519 manufacturing process Methods 0.000 description 3
- 239000000463 material Substances 0.000 description 3
- 239000003973 paint Substances 0.000 description 3
- 239000007787 solid Substances 0.000 description 3
- 238000001238 wet grinding Methods 0.000 description 3
- 229920000178 Acrylic resin Polymers 0.000 description 2
- 239000004925 Acrylic resin Substances 0.000 description 2
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 2
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 2
- 239000000020 Nitrocellulose Substances 0.000 description 2
- 239000004743 Polypropylene Substances 0.000 description 2
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 2
- 150000001338 aliphatic hydrocarbons Chemical class 0.000 description 2
- 150000004945 aromatic hydrocarbons Chemical class 0.000 description 2
- 235000014113 dietary fatty acids Nutrition 0.000 description 2
- POULHZVOKOAJMA-UHFFFAOYSA-N dodecanoic acid Chemical compound CCCCCCCCCCCC(O)=O POULHZVOKOAJMA-UHFFFAOYSA-N 0.000 description 2
- 239000003814 drug Substances 0.000 description 2
- 229940079593 drug Drugs 0.000 description 2
- 239000000194 fatty acid Substances 0.000 description 2
- 229930195729 fatty acid Natural products 0.000 description 2
- 150000004665 fatty acids Chemical class 0.000 description 2
- 238000003384 imaging method Methods 0.000 description 2
- 229910052751 metal Inorganic materials 0.000 description 2
- 239000002184 metal Substances 0.000 description 2
- 229920001220 nitrocellulos Polymers 0.000 description 2
- 239000000049 pigment Substances 0.000 description 2
- 229920001155 polypropylene Polymers 0.000 description 2
- 238000000926 separation method Methods 0.000 description 2
- 239000000377 silicon dioxide Substances 0.000 description 2
- 229920003051 synthetic elastomer Polymers 0.000 description 2
- 239000005061 synthetic rubber Substances 0.000 description 2
- ANRHNWWPFJCPAZ-UHFFFAOYSA-M thionine Chemical compound [Cl-].C1=CC(N)=CC2=[S+]C3=CC(N)=CC=C3N=C21 ANRHNWWPFJCPAZ-UHFFFAOYSA-M 0.000 description 2
- 229910000859 α-Fe Inorganic materials 0.000 description 2
- LZDKZFUFMNSQCJ-UHFFFAOYSA-N 1,2-diethoxyethane Chemical compound CCOCCOCC LZDKZFUFMNSQCJ-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
- RBTBFTRPCNLSDE-UHFFFAOYSA-N 3,7-bis(dimethylamino)phenothiazin-5-ium Chemical compound C1=CC(N(C)C)=CC2=[S+]C3=CC(N(C)C)=CC=C3N=C21 RBTBFTRPCNLSDE-UHFFFAOYSA-N 0.000 description 1
- FEIQOMCWGDNMHM-UHFFFAOYSA-N 5-phenylpenta-2,4-dienoic acid Chemical compound OC(=O)C=CC=CC1=CC=CC=C1 FEIQOMCWGDNMHM-UHFFFAOYSA-N 0.000 description 1
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 1
- YCKRFDGAMUMZLT-UHFFFAOYSA-N Fluorine atom Chemical compound [F] YCKRFDGAMUMZLT-UHFFFAOYSA-N 0.000 description 1
- 239000005639 Lauric acid Substances 0.000 description 1
- 241000208202 Linaceae Species 0.000 description 1
- 235000004431 Linum usitatissimum Nutrition 0.000 description 1
- 229910001289 Manganese-zinc ferrite Inorganic materials 0.000 description 1
- 229910001053 Nickel-zinc ferrite Inorganic materials 0.000 description 1
- 239000004677 Nylon Substances 0.000 description 1
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 1
- 239000004372 Polyvinyl alcohol Substances 0.000 description 1
- OZBDFBJXRJWNAV-UHFFFAOYSA-N Rimantadine hydrochloride Chemical compound Cl.C1C(C2)CC3CC2CC1(C(N)C)C3 OZBDFBJXRJWNAV-UHFFFAOYSA-N 0.000 description 1
- 239000002174 Styrene-butadiene Substances 0.000 description 1
- WGLPBDUCMAPZCE-UHFFFAOYSA-N Trioxochromium Chemical compound O=[Cr](=O)=O WGLPBDUCMAPZCE-UHFFFAOYSA-N 0.000 description 1
- 229920002433 Vinyl chloride-vinyl acetate copolymer Polymers 0.000 description 1
- 229910001308 Zinc ferrite Inorganic materials 0.000 description 1
- JIYIUPFAJUGHNL-UHFFFAOYSA-N [O--].[O--].[O--].[O--].[O--].[O--].[O--].[O--].[O--].[O--].[O--].[O--].[O--].[O--].[O--].[O--].[O--].[O--].[O--].[O--].[Mn++].[Mn++].[Mn++].[Fe+3].[Fe+3].[Fe+3].[Fe+3].[Fe+3].[Fe+3].[Fe+3].[Fe+3].[Fe+3].[Fe+3].[Zn++].[Zn++] Chemical compound [O--].[O--].[O--].[O--].[O--].[O--].[O--].[O--].[O--].[O--].[O--].[O--].[O--].[O--].[O--].[O--].[O--].[O--].[O--].[O--].[Mn++].[Mn++].[Mn++].[Fe+3].[Fe+3].[Fe+3].[Fe+3].[Fe+3].[Fe+3].[Fe+3].[Fe+3].[Fe+3].[Fe+3].[Zn++].[Zn++] JIYIUPFAJUGHNL-UHFFFAOYSA-N 0.000 description 1
- 229920000180 alkyd Polymers 0.000 description 1
- HSFWRNGVRCDJHI-UHFFFAOYSA-N alpha-acetylene Natural products C#C HSFWRNGVRCDJHI-UHFFFAOYSA-N 0.000 description 1
- 235000012745 brilliant blue FCF Nutrition 0.000 description 1
- MTAZNLWOLGHBHU-UHFFFAOYSA-N butadiene-styrene rubber Chemical compound C=CC=C.C=CC1=CC=CC=C1 MTAZNLWOLGHBHU-UHFFFAOYSA-N 0.000 description 1
- 239000006229 carbon black Substances 0.000 description 1
- 230000015556 catabolic process Effects 0.000 description 1
- 229920003086 cellulose ether Polymers 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 229910000423 chromium oxide Inorganic materials 0.000 description 1
- 229920001577 copolymer Polymers 0.000 description 1
- 238000007334 copolymerization reaction Methods 0.000 description 1
- 229910052802 copper Inorganic materials 0.000 description 1
- 239000010949 copper Substances 0.000 description 1
- 238000006731 degradation reaction Methods 0.000 description 1
- 238000004090 dissolution Methods 0.000 description 1
- 125000003438 dodecyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 125000002534 ethynyl group Chemical group [H]C#C* 0.000 description 1
- 238000004299 exfoliation Methods 0.000 description 1
- 239000011737 fluorine Substances 0.000 description 1
- 229910052731 fluorine Inorganic materials 0.000 description 1
- 230000004907 flux Effects 0.000 description 1
- 238000010559 graft polymerization reaction Methods 0.000 description 1
- 239000008187 granular material Substances 0.000 description 1
- 229910052742 iron Inorganic materials 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
- 238000001459 lithography Methods 0.000 description 1
- 239000000113 methacrylic resin Substances 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- 229960000907 methylthioninium chloride Drugs 0.000 description 1
- 239000000178 monomer Substances 0.000 description 1
- 231100000956 nontoxicity Toxicity 0.000 description 1
- 229920001778 nylon Polymers 0.000 description 1
- 239000012860 organic pigment Substances 0.000 description 1
- 229920001225 polyester resin Polymers 0.000 description 1
- 239000004645 polyester resin Substances 0.000 description 1
- 229920002959 polymer blend Polymers 0.000 description 1
- 238000006116 polymerization reaction Methods 0.000 description 1
- 229920005672 polyolefin resin Polymers 0.000 description 1
- 229920005749 polyurethane resin Polymers 0.000 description 1
- 229920002451 polyvinyl alcohol Polymers 0.000 description 1
- 238000007639 printing Methods 0.000 description 1
- 238000010298 pulverizing process Methods 0.000 description 1
- 239000004576 sand Substances 0.000 description 1
- 239000000344 soap Substances 0.000 description 1
- 239000003381 stabilizer Substances 0.000 description 1
- 239000011115 styrene butadiene Substances 0.000 description 1
- 229920003048 styrene butadiene rubber Polymers 0.000 description 1
- 150000005846 sugar alcohols Polymers 0.000 description 1
- 229920002803 thermoplastic polyurethane Polymers 0.000 description 1
- 230000000007 visual effect Effects 0.000 description 1
- 239000008096 xylene Substances 0.000 description 1
- WGEATSXPYVGFCC-UHFFFAOYSA-N zinc ferrite Chemical compound O=[Zn].O=[Fe]O[Fe]=O WGEATSXPYVGFCC-UHFFFAOYSA-N 0.000 description 1
Landscapes
- Liquid Developers In Electrophotography (AREA)
Abstract
Description
【発明の詳細な説明】
く産業上の利用分野〉
本発明は、マグ不1−グラフイー用液体現像剤に関し、
特に磁性トナーの分散安定性が良く、かつキャリア液体
の葎発が極めて遅い、高解像度の画像が得られるマグネ
トグラフィー用液体現像剤に関する。[Detailed Description of the Invention] Industrial Application Fields The present invention relates to a liquid developer for magnetic flux graphics.
In particular, the present invention relates to a liquid developer for magnetography that has good dispersion stability of magnetic toner, extremely slow exfoliation of carrier liquid, and is capable of producing high-resolution images.
く従来技術〉
マグネトグラフィーは、一般に表面に磁性体を有する磁
気記録媒体に磁気ヘッドを走査し磁気潜像を形威し、こ
の磁気潜像を磁性トナーで現像化後、被転写物に加圧あ
るいは、静電気的に転写し、定着することにより可視像
を得る。特に、1回の潜像形或で、現像・転写工程を繰
り返すことにより、複数枚の可視像を効率よく得られる
長所を有している。Conventional technology> Magnetography generally scans a magnetic recording medium with a magnetic material on the surface to form a magnetic latent image, and after developing this magnetic latent image with magnetic toner, pressure is applied to the transferred object. Alternatively, a visible image is obtained by electrostatically transferring and fixing. In particular, it has the advantage that a plurality of visible images can be efficiently obtained by repeating the development and transfer steps in one latent image form.
このマグネトグラフィーにおいて、可視像の品質、特に
、解像度は、用いる磁性トナーの特性により決定される
。In this magnetography, the quality of the visible image, especially the resolution, is determined by the properties of the magnetic toner used.
ところで、静電写真方式では、高解像度の可視像を得る
ために、液体現像剤が開発され、一部実用化されている
。静電写真用液体現像剤は、カーボンブランク・有機顔
料・染料等よりなる71色剤とアクリル樹脂・フェノー
ル変性アルキント樹脂・合或ゴム等の有機高分子よりな
る結着剤を主威分とし、これにレシチン・アマ二油・金
属セソケン・高級脂肪酸等の極性制御剤を添加した1・
ナーを高分子分散剤を熔解したキャリア液体中に分散し
たものである。静電写真用液体現像剤は、1・ナ表面に
静電荷を有する必要上、キャリア液体は高絶縁性・低誘
電率の溶媒である必要があり、芳香族炭化水素、あるい
は脂肪族炭化水素、例えばアイソパー(エクソン社製)
が一般に用いられている。By the way, in the electrostatic photography method, liquid developers have been developed in order to obtain high-resolution visible images, and some of them have been put into practical use. Liquid developers for electrostatic photography mainly consist of 71 colorants made of carbon blanks, organic pigments, dyes, etc., and binders made of organic polymers such as acrylic resins, phenol-modified alkint resins, and synthetic rubbers. To this, polarity control agents such as lecithin, linseed oil, metal sesoken, and higher fatty acids were added.
This is a carrier liquid in which a polymeric dispersant is dissolved. Liquid developers for electrostatic photography need to have an electrostatic charge on their surface, so the carrier liquid needs to be a solvent with high insulating properties and low dielectric constant, such as aromatic hydrocarbon, aliphatic hydrocarbon, For example, Isopar (manufactured by Exxon)
is commonly used.
静電写真用液体現像剤に用いられているこれらのキャリ
ア液体は、溶剤の極性が低く、溶解性が極め”(低いた
め、用いられる高分子分散剤の種類が限定され、1・ナ
ーの分散性が悪く、さらに揮発性でありその臭気が問題
である。These carrier liquids used in electrostatographic liquid developers have low solvent polarity and extremely high solubility (low solubility), which limits the types of polymeric dispersants that can be used and It has poor properties, is volatile, and has a problem with its odor.
マグ不1・グラフィーに液体現像剤を用いると高解像度
の可視像を効率良く得られることが期待される。しかし
、マグ不1・グラフィー用液体現像剤に関する開発例は
極めて少なく、例えば、特公昭50−40622号公報
には、磁気作用と静電気作用との組合せによる磁気印写
装置において、静電写真用液体現像剤に用いている;}
・ヤリア液体をマグネ1−グラフィー用液体現像剤のキ
ャリア液体に適用している例がある程度である。It is expected that high-resolution visible images can be efficiently obtained by using a liquid developer in magnetic imaging. However, there have been very few examples of development regarding liquid developers for magfography.For example, in Japanese Patent Publication No. 50-40622, a liquid developer for electrostatic photography was developed in a magnetic printing device that uses a combination of magnetic action and electrostatic action. Used in developer; }
- There are some cases in which Yaria liquid is used as a carrier liquid for liquid developers for magnetography.
〈発明が解決しようとする課題〉
本発明は、従来知られているマグネ1−グラフィにおい
て、液体現像剤の組威を検J・1ずることにより、適度
な極性溶剤であり、磁性トナーの分散安定性が良く、か
つキャリア液体の華発が極めて遅く、かつ高解像度の可
視像が得られるマグ不1〜グラフィー用液体現像剤に関
するものである。<Problems to be Solved by the Invention> The present invention has been developed by examining the composition strength of a liquid developer in conventionally known magnetography. The present invention relates to a liquid developer for magnetic graphics that has good stability, extremely slow blooming of the carrier liquid, and provides visible images with high resolution.
〈課題を解失するための手段〉
本発明は、上述の現状に鑑メてなされたものであり、具
体的には、一般r(の
H 3 C −0 −C 一( C I .),l−C
−O −C II .1111
0 0 ・・■
で示される溶媒八を主威分とするキャリア液体中に、磁
性粒子と着色剤および結合剤を主戒分とする磁性l・ナ
ーを分散してなるマグネ1・グラフィーJTI /Pj
.体現像剤を提供するものであり、磁性1−ナーの分散
安定性が良く、かつキャリア液体の蒸発が極めて遅く、
高解像度の可視像が得られるマグネI・グラフィー用液
体現像剤を提仇ずるものである。<Means for Solving the Problems> The present invention has been made in view of the above-mentioned current situation, and specifically, H3C-0-C1(CI.) of general r(), l-C
-O-C II. 1111 0 0 . . . Magne 1 GRAPH JTI, which is made by dispersing magnetic particles, a coloring agent, and a binder as main components in a carrier liquid whose main components are a solvent 8 represented by /Pj
.. The magnetic 1-ner has good dispersion stability, and the carrier liquid evaporates very slowly.
The present invention proposes a liquid developer for Magne I graphics that can provide high-resolution visible images.
〈発明の詳述〉 以下本発明をさらに詳細に説明する。<Detailed description of the invention> The present invention will be explained in more detail below.
木発明によるマグ不トグラフィー用液体現像剤の代表的
構成は、キャリア?夜体 このキャリア液体に溶解する
有機高分子からなる高分子分散剤・磁性トナー・分散助
剤である。What is the typical composition of the liquid developer for mag lithography invented by Kiyoshi? Night Body Polymer dispersant, magnetic toner, and dispersion aid made of organic polymers that dissolve in this carrier liquid.
本発明における最も重要な横成部分であるキャリア液体
は、安全性・低揮発性・非毒性・低臭性を満足し、かつ
磁性トナーの分散安定性を保つ必要がある。また、磁性
トナーが静電荷を持つ必要がなく、従来の静電写真用液
体現像剤に用いられている高絶縁性・低誘電率の脂肪族
炭化水素や芳香族炭化水素系溶媒である必要はない。The carrier liquid, which is the most important component in the present invention, must satisfy safety, low volatility, nontoxicity, and low odor, and must maintain dispersion stability of the magnetic toner. In addition, the magnetic toner does not need to have an electrostatic charge, and it does not need to be a highly insulating, low dielectric constant aliphatic hydrocarbon or aromatic hydrocarbon solvent used in conventional electrostatic photographic liquid developers. do not have.
本発明者は、上記の要件を満たすべく種々の溶剤を検利
した結果、マグ不トグラフィー用液体現像剤に用いるキ
ャリア液体は、一般弐の1−13 C−○−C −(
C I .). 一C −0 −C Ii .1111
0 0 ・・■
で示される溶媒八を主威分とするキャリア液体が最適で
あることを見出した。As a result of testing various solvents to meet the above requirements, the present inventor found that the carrier liquid used in the liquid developer for mag nontography is general 2 1-13 C-○-C-(
CI. ). 1C -0 -C Ii. 1111 0 0...■
It has been found that a carrier liquid containing the solvent 8 as the main component is optimal.
一般弐ので示される溶媒八を主成分とする−1−ヤリア
液体は、分子内に非極性基のアルキル基を有し、かつ極
性基のアシル基を有している。このため、キャリア液体
の極性が制御でき、磁性1・ナーの分散性が極めてよい
。また、一般式ので示される溶剤Aは、揮発性が低く、
さらに有機高分子の溶解性も適度にあり、磁性1・ナー
の分散に最も適する高分子分散剤を選択する事が可能で
ある。The -1-Yaria liquid, which is mainly composed of solvent 8 shown in General 2, has an alkyl group, which is a nonpolar group, and an acyl group, which is a polar group, in the molecule. Therefore, the polarity of the carrier liquid can be controlled, and the dispersibility of the magnetic 1.ner is extremely good. In addition, solvent A represented by the general formula has low volatility,
Furthermore, the solubility of the organic polymer is moderate, and it is possible to select a polymer dispersant most suitable for dispersing magnetic 1.ner.
上述のキャリア液体は、用いる磁性トナーの構成および
用いるマグネトグラフィーの用途により適宜選択される
必要がある。また、2種類以上の一般式ので示される溶
媒を混合して用いること、一般式■で示される溶媒と高
級アルコールおよび高級アルコール誘導体、一般式ので
示される溶媒と多価アルコールおよびその誘導体の混合
物をキャリア液体に用いることにより、キャリア液体の
揮発速度・溶解能・磁性1・ナーの分散安定性を制御す
るのに有効である。The carrier liquid described above needs to be appropriately selected depending on the composition of the magnetic toner used and the application of the magnetography used. In addition, it is also possible to use a mixture of two or more solvents represented by the general formula, mixtures of the solvent represented by the general formula (1) and higher alcohols and higher alcohol derivatives, and mixtures of the solvent represented by the general formula and polyhydric alcohols and their derivatives. When used in a carrier liquid, it is effective in controlling the volatilization rate, dissolution ability, magnetic 1, and dispersion stability of the carrier liquid.
磁性1・ナーは、磁性粒子・顔料および染料からなる着
色剤・有機高分子からなる結着剤を主或分とする。Magnetic 1-ner mainly consists of magnetic particles, a coloring agent made of pigments and dyes, and a binder made of an organic polymer.
磁性粒子は、鉄・コハルト・酸化クロム・ニノケルジン
クフエライト、マンガンジンクフエライト等の各種フエ
ライl・等一般に知られている磁性体が用いられ、その
粒子径は、用いる磁性トナーの用途により決定されるが
、0,01μrn〜10μm好ましくは、0.03μm
〜1.0μmである。As the magnetic particles, commonly known magnetic materials such as iron, cohardt, chromium oxide, various ferrites such as nylon zinc ferrite, manganese zinc ferrite, etc. are used, and the particle size is determined depending on the purpose of the magnetic toner used. However, 0.01 μrn to 10 μm, preferably 0.03 μm
~1.0 μm.
また、着色剤は、本発明において特に指定されるもので
はなく、静電写真用トナーに用いられている様な公知の
各種顔料および染料を使用することができる。イ列えば
、アセチレンフ゛ラ・冫ク・ケノヂエンフ゛ラソク等の
カーボンフ゛ラ・冫ク、ニグロシン、メチレンブルー
フタ口シアニンブルーなどが挙げられる。Further, the colorant is not particularly specified in the present invention, and various known pigments and dyes such as those used in electrostatic photographic toners can be used. For example, acetylene filler/drug, carbon filler/drug such as chenodiene filler, nigrosine, methylene blue.
Examples include lid cyanine blue.
結着剤は、上述のキャリア液体に熔解せず、被転写物に
対し転写定着性を有する必要があり、ウレタン樹脂・セ
ルロースエーテル樹脂・ポリエステル樹脂・アクリル樹
脂・メタクリル樹脂・スチレン樹脂・ポリオレフィン樹
脂・フェノール変性アルキッド樹脂・合成ゴム等、ある
いは、これらのポリマーブレンドおよび共重合樹脂等、
一般に用いられている有機高分子から選択できる。The binder must not be dissolved in the above-mentioned carrier liquid and must have transfer-fixing properties to the transferred material, such as urethane resin, cellulose ether resin, polyester resin, acrylic resin, methacrylic resin, styrene resin, polyolefin resin, etc. Phenol-modified alkyd resin, synthetic rubber, etc., or their polymer blends and copolymer resins, etc.
It can be selected from commonly used organic polymers.
高分子分散剤は、キャリア液体の種類および、上述の様
に構成した磁性1・ナーの種類により、適宜決定される
。一般に高分子分散剤は、キャリア液体に可溶なセグメ
ントと難溶性のセグメン1・を有するブロックボリマー
、あるいは、共重合ボリマーが好適である。特にこの難
溶性セグメン1・が磁性1・ナーの結着剤と類似の化学
構造を有するものが、磁性トナーを安定に分散さ一已る
。また、この高分子分敗剤が磁性1・ナーの表面に吸着
あるいは、化学結合、または、磁性1・ナーに練り込ま
れている場合、高分子分散剤の立体的反発力により磁性
トナーを安定に分散出来る。この高分子分散剤は、各種
のモノマーの共重合・グラフト重合・ブロック重合によ
り得られるが、これらの方法に限定されるものではなく
種々の方法が考えられる。The polymeric dispersant is appropriately determined depending on the type of carrier liquid and the type of magnetic 1-ner configured as described above. Generally, the polymer dispersant is preferably a block polymer or a copolymer polymer having a segment soluble in the carrier liquid and a segment 1 that is sparingly soluble in the carrier liquid. In particular, when the poorly soluble segment 1. has a chemical structure similar to the binder of the magnetic 1.ner, the magnetic toner can be stably dispersed. In addition, if this polymeric dispersing agent is adsorbed to the surface of the magnetic 1-toner, chemically bonded, or kneaded into the magnetic 1-toner, the steric repulsion of the polymeric dispersant stabilizes the magnetic toner. It can be dispersed into This polymer dispersant can be obtained by copolymerization, graft polymerization, or block polymerization of various monomers, but the method is not limited to these methods and various methods can be used.
さらに、磁性1〜ナーがキャリア肢体中に良好に分散し
ている場合、高分子分敗安定剤を添加する必要↓4ない
。Furthermore, if the magnetic materials are well dispersed in the carrier body, there is no need to add polymeric degradation stabilizers.
また、分敗助剤は、磁性1・ナーの分散性を向」ニさせ
るものであり、各種界面活性剤、低級アルコルおよびこ
の誘導体、金属セッケン、アマ二泊、高級脂肪酸、シリ
カ微粉末等が用いられる。In addition, the separation aids are those that improve the dispersibility of the magnetic 1-ner, and include various surfactants, lower alcohols and their derivatives, metal soaps, flax, higher fatty acids, and fine silica powder. used.
さらに、キャリア液体に可溶な高分子を添加し、磁性ト
ナーの被転写物への転写定着性を向上さーl゛ることも
可能である。Furthermore, it is also possible to add a soluble polymer to the carrier liquid to improve the transfer and fixing properties of the magnetic toner to the transferred object.
本発明によるマグ不I・グラフィー用液体現像剤の製造
方法は、従来公知の静電写真用液体現像剤の製造方法が
適用できる。以下その製造方法の一例を示す。As the method for producing the liquid developer for magnetic imaging according to the present invention, a conventionally known method for producing a liquid developer for electrostatic photography can be applied. An example of the manufacturing method will be shown below.
上述の磁性粒子・着色剤・結着剤、また必要があれば界
面活性剤を添加し、この結着剤のm溶媒中で、ボールミ
ル・ロールミル・ペイントシエ−カー・3本ロール等の
混練機によりl昆練後l昆練物を得、該親溶媒を加熱等
により除去し7昆合物を得る。あるいは、前記混練物を
該結着剤を溶解しない溶媒に注入し、該結着剤の析出に
より、混合物を得る。あるいは、磁性拉子・着色剤・結
着剤また、必要があれば界面活性剤を該結着剤の軟化点
以上で加熱しながら、ニーダー・3本ロール等の混練機
により混練後混合物を得る。この様にして得られた混合
物を乾式粉砕法、あるい6J.溶媒とともに粉砕する湿
式粉砕法により磁性1・ナーを得る。湿式粉砕時の溶媒
は、本発明のキャリア液体を用いても良く、また、前記
結着剤の親溶媒を1〜20部添加しても良い。Add the above-mentioned magnetic particles, colorant, binder, and if necessary a surfactant, and knead in a ball mill, roll mill, paint shaker, three-roll, etc. solvent in the binder. After 1 kneading, a 1 kneaded product is obtained, and the parent solvent is removed by heating or the like to obtain a 7 kneaded product. Alternatively, the kneaded material is poured into a solvent that does not dissolve the binder, and the binder is precipitated to obtain a mixture. Alternatively, the mixture is obtained after kneading with a kneader such as a kneader or three rolls while heating the magnetic spatula, colorant, binder, and, if necessary, a surfactant above the softening point of the binder. . The mixture thus obtained is subjected to dry pulverization method or 6J. A magnetic 1.ner is obtained by a wet grinding method in which the material is ground together with a solvent. As the solvent for wet grinding, the carrier liquid of the present invention may be used, or 1 to 20 parts of the parent solvent of the binder may be added.
この様にして得られた磁性1〜ナーに、本発明のキャリ
ア液体と必要ならば」一述した高分子分散剤・分散助剤
・キャリア液体に可溶な高分子を添加し、マグネ1・グ
ラフィー用液体現像剤を得る。高分子分散剤、・分敗助
剤の添加方法は、上記方法以外にl昆練時あるいは、湿
式粉砕時に添加しても良く、それらを併用しても良い。The carrier liquid of the present invention and, if necessary, the above-mentioned polymeric dispersant, dispersion aid, and polymer soluble in the carrier liquid are added to the thus obtained Magnetic 1 to 1. A liquid developer for graphics is obtained. In addition to the methods described above, the polymer dispersant and the separation aid may be added during kneading or wet grinding, or they may be added in combination.
マグネトグラフィー用液体現像剤中の磁性]ヘナーの濃
度は特に限定されないが、本発明のキャリア液体に対し
0.01wt%〜1.Owt%程度である。また、高分
子分散剤の濃度は、使用時においてO.OO1wt%〜
Q,lwt%に調整するのが好ましいが、特に限定され
るものではなく、適宜決定される。The concentration of [Magnetic] hener in the liquid developer for magnetography is not particularly limited, but is 0.01 wt% to 1.0 wt% with respect to the carrier liquid of the present invention. It is about Owt%. In addition, the concentration of the polymer dispersant is O. OO1wt%~
Although it is preferable to adjust Q, lwt%, it is not particularly limited and can be determined as appropriate.
〈作用〉
本発明による、マグネトグラフィー用液体現像剤におい
て、液体現像剤の組或を検討することにより、トナーの
分散安定性が良く、かつキャリア液体の華発が極めて遅
く、かつ高解像度の可視像が得られるマグ不トグラフィ
ー用液体現像剤が得られる。<Function> In the liquid developer for magnetography according to the present invention, by considering the composition of the liquid developer, it is possible to achieve good toner dispersion stability, extremely slow blooming of the carrier liquid, and high resolution. A liquid developer for mag atonography from which a visual image can be obtained is obtained.
〈実施例〉 以下実施例により具体的に説明する。<Example> This will be explained in detail below using Examples.
実施例1.
結着剤
・スヂレンーアクリル酸エステル共重合樹脂75重量部
・メラ旦ン樹脂 10重量部・塩素
化ボリプロビレン I5重量部着色剤
・カーボンブラック 10重量部磁性粒
子
ニッケルジンクフエライト微粉末
(平均粒径0.03μm) I O重量部界面活性剤
・弗素系界面活性剤 0,1重量部をメチ
ルエチルケトンを用いペイントシェーカーにより混練後
、示性式
H.C一〇一C 一( C H Z) 2−C −0
−C H I+l111
00
で示される溶媒剤よりなるキャリア液体500m1を添
加し、加熱によりメチルエチルゲ1・ンを華発させ、混
合物Aを得た。この混合物Aをさらにペイントシェーカ
ーにより湿式粉砕し、平均顆径0.36μmの磁性トナ
ーを得た。Example 1. Binder: 75 parts by weight of styrene-acrylic acid ester copolymer resin, 10 parts by weight of Meradan resin, 5 parts by weight of chlorinated polypropylene I Colorant: 10 parts by weight Carbon black Magnetic particles Nickel zinc ferrite fine powder (average particles) After kneading 0.1 parts by weight of IO surfactant and fluorine-based surfactant in a paint shaker using methyl ethyl ketone, it was mixed with the following formula H. C101C 1 (C H Z) 2-C -0
500 ml of a carrier liquid consisting of a solvent represented by -C H I+l111 00 was added, and methyl ethylgein was ignited by heating to obtain a mixture A. This mixture A was further wet-pulverized using a paint shaker to obtain a magnetic toner having an average granule diameter of 0.36 μm.
さらに、ラウリル酸で部分ケン化したポリビニルアルコ
ールからなる高分子分散剤を溶解した前記キャリア液体
500mlを添加後、シリヵ微粉末(粒径0.03μm
)2gよりなる分散助剤を添加し、固形分濃度1.5w
t%になるようにキヤリア液体で調整し、マグネトグラ
フィー用液体現像剤を得た。Furthermore, after adding 500 ml of the carrier liquid in which a polymeric dispersant made of polyvinyl alcohol partially saponified with lauric acid was added, fine silica powder (particle size 0.03 μm) was added.
) 2g of dispersion aid was added to make the solid content concentration 1.5w.
A liquid developer for magnetography was obtained by adjusting with a carrier liquid so that the developer was t%.
上述のマグネトグラフィー用液体現像剤は、30日間経
過後の磁性トナーの再分散が良く、さらにキャリア液体
の舊発も5%以下であった。また、湿式マグネトグラフ
ィー現像機により、5μmの細線を顕像できた。The above-mentioned liquid developer for magnetography showed good redispersion of magnetic toner after 30 days, and expulsion of carrier liquid was 5% or less. Furthermore, a fine line of 5 μm could be developed using a wet magnetography developing machine.
実施例2.
結着剤
・マレイン酸変性ポリプロピレン 100重量部着色剤
・カーポンブランク 10重量部・銅フ
タ口シアニン 1重量部磁性粒子
・フェライ1〜微粉末(平均粒径0,12μm)】0重
量部
を3本ロールで混練し、混合物Bを得た。Example 2. Binder - 100 parts by weight of maleic acid-modified polypropylene Colorant - 10 parts by weight Carpon blank - 1 part by weight of copper cap cyanine Mixture B was obtained by kneading with a roll.
二の混合物Bに結着剤に対し親溶媒のキシレン5重量部
と、示性式
で示される溶媒剤よりなるキャリア液体500m1を加
え、ボールくルにより45時間粉砕し、平均粒径0.6
0μmの磁性トナーを得た。5 parts by weight of xylene, which is a parent solvent, and 500 ml of a carrier liquid consisting of a solvent shown by the formula for the binder were added to the second mixture B, and the mixture was ground with a ball mill for 45 hours, and the average particle size was 0.6.
A magnetic toner with a diameter of 0 μm was obtained.
さらに、スチレン−ブタジエンブロックボリマからなる
高分子分散剤・ニトロセルロースよりなるキャリア液体
に可溶な高分子を添加し、固形分濃度l,5wt%にな
るように前記キャリア液体で調整し、マグネトグラフィ
ー用液体現像剤を得た。Furthermore, a soluble polymer is added to a polymer dispersant made of styrene-butadiene block polymer and a carrier liquid made of nitrocellulose, and the solid content is adjusted to 1.5 wt% with the carrier liquid. A liquid developer for graphics was obtained.
上述のマグネトグラフィー用液体現像剤は、30日間経
過後の磁性トナーの再分散が良く、さらにキャリア液体
の舊発も5%以下であった。また、湿式マグネトグラフ
ィー現像機により、5μmの細線を顕像できた。The above-mentioned liquid developer for magnetography showed good redispersion of magnetic toner after 30 days, and expulsion of carrier liquid was 5% or less. Furthermore, a fine line of 5 μm could be developed using a wet magnetography developing machine.
実施例3.
結着剤
・ポリウレタン樹脂 80重量部・エボ
キシ系樹脂 20重量部・塩ビ−酢酸
ビニル共重合樹脂 lO重景部着色剤
・カーボンプラック 10重量部・メヂ
レンブル− 1重量部磁性粒子
・フエライト微粉末(平均粒径0.l2μm)10重量
部
界面活性剤
・弗素系界面活性剤 0.1重量部にエチ
レングリコールジエチルエーテル500重量部を加え、
サンドξルで混練し、混合物Cを得た。Example 3. Binder - Polyurethane resin 80 parts by weight - Eboxy resin 20 parts by weight - Vinyl chloride-vinyl acetate copolymer resin IO heavy area Colorant - Carbon plaque 10 parts by weight - Medielene blue - 1 part by weight Magnetic particles - Fine ferrite powder (average Add 500 parts by weight of ethylene glycol diethyl ether to 0.1 parts by weight of surfactant/fluorosurfactant (particle size: 0.12 μm),
Mixture C was obtained by kneading in a sand mill.
この混合物Cに示性式
で示される溶媒剤よりなるキャリア液体1000mlを
添加し、サントミルにより粉砕し、平均粒径0.34μ
mの磁性1・ナーを得た。To this mixture C, 1000 ml of a carrier liquid consisting of a solvent shown by the formula was added, and the mixture was pulverized with a Santo mill, and the average particle size was 0.34μ.
A magnetic 1·ner of m was obtained.
さらに、ラウリルメタクリレ−1・と2−ヒドロキシル
メタクリレ−1・の共重合樹脂からなる高分子分散剤・
ニトロセルロースよりなるキャリア液体に可溶な高分子
を添加し、固形分濃度1−5wt%になるように前記キ
ャリア液体で調整し、マグネトグラフィー用液体現像剤
を得た。Furthermore, a polymer dispersant consisting of a copolymer resin of lauryl methacrylate-1 and 2-hydroxyl methacrylate-1
A soluble polymer was added to a carrier liquid made of nitrocellulose, and the solid content concentration was adjusted to 1-5 wt% with the carrier liquid to obtain a liquid developer for magnetography.
上述のマグネトグラフィー用液体現像剤は、30日間経
過後の磁性トナーの再分散が良《、さらにキャリア液体
の蒸発も5%以下であった。また、湿式マグネトグラフ
ィー現像機により、5μmの細線を顕像できた。The above liquid developer for magnetography showed good redispersion of the magnetic toner after 30 days, and evaporation of the carrier liquid was 5% or less. Furthermore, a fine line of 5 μm could be developed using a wet magnetography developing machine.
く発明の効果〉
本発明は、上述の如くであり、マグネトグラフィー用液
体現像剤において、液体現像剤の組成を検討することに
より、トナーの分散安定性が良く、かつキャリア液体の
蒸発が極めて遅く、かつ高解像度の可視像が得られるマ
グネ1・グラフィー用液体現像剤を提供できた。Effects of the Invention> The present invention is as described above, and by considering the composition of the liquid developer in a liquid developer for magnetography, the dispersion stability of the toner is good and the evaporation of the carrier liquid is extremely slow. We were able to provide a liquid developer for magnetography that can provide a high-resolution visible image.
Claims (1)
非画線部とからなる磁気潜像をマグネトグラフィー用液
体現像剤で現像し、被転写物に転写定着し、可視像を得
るマグネトグラフィーにおいて、このマグネトグラフィ
ー用液体現像剤が、一般式(1) ▲数式、化学式、表等があります▼・・・(1) で示される溶媒Aを主成分とするキャリア液体中に、磁
性粒子と着色剤および結合剤を主成分とする磁性トナー
を分散してなるマグネトグラフィー用液体現像剤。(1) A magnetic latent image consisting of a magnetized image area and a non-magnetized non-image area is developed on a magnetic material using a liquid developer for magnetography, and is transferred and fixed onto the transfer target, resulting in a visible image. In magnetography, the liquid developer for magnetography is mixed into a carrier liquid containing solvent A as the main component represented by general formula (1) ▲Mathematical formula, chemical formula, table, etc. , a liquid developer for magnetography comprising a magnetic toner containing magnetic particles, a colorant, and a binder as main components dispersed therein.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP1164576A JPH0329961A (en) | 1989-06-27 | 1989-06-27 | Liquid developer for magnetography |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP1164576A JPH0329961A (en) | 1989-06-27 | 1989-06-27 | Liquid developer for magnetography |
Publications (1)
Publication Number | Publication Date |
---|---|
JPH0329961A true JPH0329961A (en) | 1991-02-07 |
Family
ID=15795795
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP1164576A Pending JPH0329961A (en) | 1989-06-27 | 1989-06-27 | Liquid developer for magnetography |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH0329961A (en) |
Cited By (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2008045063A (en) * | 2006-08-18 | 2008-02-28 | Fuji Xerox Co Ltd | Printing liquid for image formation and image formation apparatus |
JP2008063552A (en) * | 2006-08-08 | 2008-03-21 | Fuji Xerox Co Ltd | Image-forming recording liquid and image-forming device |
JP2009271132A (en) * | 2008-04-30 | 2009-11-19 | Fuji Xerox Co Ltd | Liquid developing agent, process cartridge, and image forming device |
US8304154B2 (en) | 2009-03-27 | 2012-11-06 | Fuji Xerox Co., Ltd. | Particle dispersion liquid, particles, particle dispersion liquid cartridge, process cartridge, image forming apparatus, and image forming method |
WO2017142065A1 (en) * | 2016-02-19 | 2017-08-24 | 東洋インキScホールディングス株式会社 | Liquid developer and method for producing printed material using same |
-
1989
- 1989-06-27 JP JP1164576A patent/JPH0329961A/en active Pending
Cited By (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2008063552A (en) * | 2006-08-08 | 2008-03-21 | Fuji Xerox Co Ltd | Image-forming recording liquid and image-forming device |
US7722711B2 (en) | 2006-08-08 | 2010-05-25 | Fuji Xerox Co., Ltd. | Image-forming recording liquid and image-forming device |
JP2008045063A (en) * | 2006-08-18 | 2008-02-28 | Fuji Xerox Co Ltd | Printing liquid for image formation and image formation apparatus |
JP2009271132A (en) * | 2008-04-30 | 2009-11-19 | Fuji Xerox Co Ltd | Liquid developing agent, process cartridge, and image forming device |
US8304154B2 (en) | 2009-03-27 | 2012-11-06 | Fuji Xerox Co., Ltd. | Particle dispersion liquid, particles, particle dispersion liquid cartridge, process cartridge, image forming apparatus, and image forming method |
WO2017142065A1 (en) * | 2016-02-19 | 2017-08-24 | 東洋インキScホールディングス株式会社 | Liquid developer and method for producing printed material using same |
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