JPS6339050B2 - - Google Patents
Info
- Publication number
- JPS6339050B2 JPS6339050B2 JP56038146A JP3814681A JPS6339050B2 JP S6339050 B2 JPS6339050 B2 JP S6339050B2 JP 56038146 A JP56038146 A JP 56038146A JP 3814681 A JP3814681 A JP 3814681A JP S6339050 B2 JPS6339050 B2 JP S6339050B2
- Authority
- JP
- Japan
- Prior art keywords
- toner
- magnetic
- weight
- parts
- sno
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired
Links
- 239000000843 powder Substances 0.000 claims description 19
- 229910006404 SnO 2 Inorganic materials 0.000 claims description 18
- 239000006247 magnetic powder Substances 0.000 claims description 13
- 239000011230 binding agent Substances 0.000 claims description 9
- 238000000034 method Methods 0.000 description 24
- 239000011347 resin Substances 0.000 description 10
- 229920005989 resin Polymers 0.000 description 10
- 230000007613 environmental effect Effects 0.000 description 9
- 230000007423 decrease Effects 0.000 description 7
- 238000011161 development Methods 0.000 description 7
- 230000018109 developmental process Effects 0.000 description 7
- -1 for example Substances 0.000 description 6
- 238000012360 testing method Methods 0.000 description 6
- SZVJSHCCFOBDDC-UHFFFAOYSA-N iron(II,III) oxide Inorganic materials O=[Fe]O[Fe]O[Fe]=O SZVJSHCCFOBDDC-UHFFFAOYSA-N 0.000 description 4
- 229910052751 metal Inorganic materials 0.000 description 4
- 239000002184 metal Substances 0.000 description 4
- 150000002739 metals Chemical class 0.000 description 4
- 238000002156 mixing Methods 0.000 description 4
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 3
- 238000007792 addition Methods 0.000 description 3
- 239000003795 chemical substances by application Substances 0.000 description 3
- 239000008119 colloidal silica Substances 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- 239000000463 material Substances 0.000 description 3
- 239000002245 particle Substances 0.000 description 3
- 239000000126 substance Substances 0.000 description 3
- 238000012546 transfer Methods 0.000 description 3
- 229910002012 Aerosil® Inorganic materials 0.000 description 2
- 239000004698 Polyethylene Substances 0.000 description 2
- 229910010413 TiO 2 Inorganic materials 0.000 description 2
- 230000000052 comparative effect Effects 0.000 description 2
- 239000000975 dye Substances 0.000 description 2
- 239000010419 fine particle Substances 0.000 description 2
- 230000002209 hydrophobic effect Effects 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- 108091008695 photoreceptors Proteins 0.000 description 2
- 239000000049 pigment Substances 0.000 description 2
- 229920000573 polyethylene Polymers 0.000 description 2
- 229920000642 polymer Polymers 0.000 description 2
- 239000002904 solvent Substances 0.000 description 2
- 238000003860 storage Methods 0.000 description 2
- 150000003505 terpenes Chemical class 0.000 description 2
- 235000007586 terpenes Nutrition 0.000 description 2
- 239000001993 wax Substances 0.000 description 2
- RSWGJHLUYNHPMX-UHFFFAOYSA-N Abietic-Saeure Natural products C12CCC(C(C)C)=CC2=CCC2C1(C)CCCC2(C)C(O)=O RSWGJHLUYNHPMX-UHFFFAOYSA-N 0.000 description 1
- 239000004952 Polyamide Substances 0.000 description 1
- 239000004743 Polypropylene Substances 0.000 description 1
- 239000004793 Polystyrene 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
- 230000002378 acidificating effect Effects 0.000 description 1
- 125000001931 aliphatic group Chemical group 0.000 description 1
- 229920001400 block copolymer Polymers 0.000 description 1
- CSYSJPRFLYSSOB-UHFFFAOYSA-N butyl 2-methylprop-2-enoate;furan-2,5-dione;styrene Chemical compound O=C1OC(=O)C=C1.C=CC1=CC=CC=C1.CCCCOC(=O)C(C)=C CSYSJPRFLYSSOB-UHFFFAOYSA-N 0.000 description 1
- 229910000420 cerium oxide Inorganic materials 0.000 description 1
- 238000004581 coalescence Methods 0.000 description 1
- 239000011248 coating agent Substances 0.000 description 1
- 238000000576 coating method Methods 0.000 description 1
- 235000014113 dietary fatty acids Nutrition 0.000 description 1
- 239000000194 fatty acid Substances 0.000 description 1
- 229930195729 fatty acid Natural products 0.000 description 1
- UPBDXRPQPOWRKR-UHFFFAOYSA-N furan-2,5-dione;methoxyethene Chemical compound COC=C.O=C1OC(=O)C=C1 UPBDXRPQPOWRKR-UHFFFAOYSA-N 0.000 description 1
- 230000004927 fusion Effects 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 239000011810 insulating material Substances 0.000 description 1
- 229920000554 ionomer Polymers 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 239000000696 magnetic material Substances 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 229910044991 metal oxide Inorganic materials 0.000 description 1
- 150000004706 metal oxides Chemical class 0.000 description 1
- 239000000025 natural resin Substances 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- BMMGVYCKOGBVEV-UHFFFAOYSA-N oxo(oxoceriooxy)cerium Chemical compound [Ce]=O.O=[Ce]=O BMMGVYCKOGBVEV-UHFFFAOYSA-N 0.000 description 1
- 239000012188 paraffin wax Substances 0.000 description 1
- WXZMFSXDPGVJKK-UHFFFAOYSA-N pentaerythritol Chemical compound OCC(CO)(CO)CO WXZMFSXDPGVJKK-UHFFFAOYSA-N 0.000 description 1
- 239000003208 petroleum Substances 0.000 description 1
- 239000005011 phenolic resin Substances 0.000 description 1
- 229920002647 polyamide Polymers 0.000 description 1
- 229920000728 polyester Polymers 0.000 description 1
- 229920001155 polypropylene Polymers 0.000 description 1
- 229920002223 polystyrene Polymers 0.000 description 1
- 229920000036 polyvinylpyrrolidone Polymers 0.000 description 1
- 239000001267 polyvinylpyrrolidone Substances 0.000 description 1
- 235000013855 polyvinylpyrrolidone Nutrition 0.000 description 1
- 238000003825 pressing Methods 0.000 description 1
- 238000012827 research and development Methods 0.000 description 1
- 239000007779 soft material Substances 0.000 description 1
- 229920003002 synthetic resin Polymers 0.000 description 1
- 239000000057 synthetic resin Substances 0.000 description 1
- 229920005992 thermoplastic resin Polymers 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
- 229910000859 α-Fe Inorganic materials 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
- G03G9/097—Plasticisers; Charge controlling agents
- G03G9/09708—Inorganic compounds
Description
【発明の詳細な説明】
本発明は電子写真法或いは静電印刷法などに於
いて、電気的潜像または磁気的潜像を現像するの
に用いられる磁性トナーに関するものである。DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a magnetic toner used for developing an electrical latent image or a magnetic latent image in electrophotography or electrostatic printing.
従来、電子写真法としては米国特許第2297691
号明細書、特公昭42―23910号公報及び特公昭43
―24748号公報等に記載されている如く、多数の
方法が知られているが、一般には光導電性物質を
利用し、種々の手段により感光体上に電気的潜像
を形成し、次いで該潜像をトナーを用いて現像
し、必要に応じて紙等の転写材にトナー画像を転
写した後、加熱、圧力或いは溶剤蒸気などにより
定着し複写物を得るものである。 Conventionally, as an electrophotographic method, U.S. Patent No. 2297691
Specification, Special Publication No. 42-23910 and Special Publication No. 43
A number of methods are known, as described in Japanese Patent Application No. 24748, etc., but in general, a photoconductive substance is used to form an electrical latent image on a photoreceptor by various means, and then the photoreceptor is A latent image is developed using toner, and after the toner image is transferred to a transfer material such as paper as necessary, it is fixed by heat, pressure, solvent vapor, etc. to obtain a copy.
また、電気的潜像をトナーを用いて可視化する
方法も種々知られている。例えば米国特許第
2874063号明細書に記載されている磁気ブラシ法、
同2618552号明細書に記載されているカスケード
現像法及び同2221776号明細書に記載されている
粉末雲法及びフアーブラシ現像法、液体現像法等
多数の現像法が知られている。これらの現像法等
に用いられるトナーとしては、従来、天然或いは
合成樹脂中に染料、顔料を分散させた微粉末が使
用されている。更に、第3物質を種々の目的で添
加した現像微粉末を使用することも知られてい
る。 Various methods are also known for visualizing electrical latent images using toner. For example, US Patent No.
The magnetic brush method described in specification No. 2874063,
A large number of development methods are known, such as the cascade development method described in No. 2,618,552, the powder cloud method, the fur brush development method, and the liquid development method described in No. 2,221,776. Toners used in these developing methods have conventionally been fine powders in which dyes and pigments are dispersed in natural or synthetic resins. Furthermore, it is also known to use fine developing powder to which a third substance is added for various purposes.
現像されたトナー画像は、必要に応じて紙など
の転写材に転写され定着される。 The developed toner image is transferred and fixed onto a transfer material such as paper, if necessary.
トナー画像の定着方法としては、トナーをヒー
ター或いは熱ローラー等により加熱焙融して支持
体に融着固化させる方法、有機溶剤によりトナー
のバインダー樹脂を軟化或いは溶解し支持体に定
着する方法、加圧によりトナーを支持体に定着す
る方法等が知られている。 Methods for fixing toner images include heating and melting the toner with a heater or hot roller to fuse and solidify it to the support, softening or dissolving the binder resin of the toner with an organic solvent, and fixing it to the support. A method of fixing toner on a support by pressure is known.
トナーは夫々の定着法に適するように材料を選
択され、特定の定着法に使用されるトナーは他の
定着法に使用できないのが一般的である。特に、
従来広く行なわれているヒーターによる熱融着定
着法に用いるトナーを熱ローラー定着法、溶剤定
着法、圧力定着法などに転用することはほとんど
不可能である。従つて、夫々の定着法に適したト
ナーが研究開発されている。 Toner materials are selected to be suitable for each fixing method, and toners used for a particular fixing method generally cannot be used for other fixing methods. especially,
It is almost impossible to transfer the toner used in the conventionally widely used heat fusion fixing method using a heater to a hot roller fixing method, a solvent fixing method, a pressure fixing method, or the like. Therefore, toners suitable for each fixing method are being researched and developed.
トナーを加圧により定着する方法は米国特許第
3269626号明細書、特公昭46―15876号公報などに
記載されており、省エネルギー、無公害、複写機
の電源を入れれば待時間なしで複写が行えるこ
と、コピーの焼け焦げの危険もないこと、高速定
着が可能なこと及び定着装置が簡単であることな
ど利点が多い。 The method of fixing toner by applying pressure is based on US Patent No.
It is described in specification No. 3269626, Japanese Patent Publication No. 46-15876, etc., and is energy saving, non-polluting, copying can be done without waiting time when the copying machine is turned on, there is no risk of burning copies, and high speed. It has many advantages such as being able to be fixed and having a simple fixing device.
しかし、トナーの定着性、加圧ローラーへのオ
フセツト現像など問題点もあり、加圧定着法の改
善の為に種々の研究開発が行われている。例えば
特公昭44―9880号公報には脂肪族成分と熱可塑性
樹脂を含む圧力定着トナーが記載されており、特
開昭48―75032号、同48―78931号、同49―17739
号、同52―108134号などには核に軟質物質を含ん
だカプセル型の圧力定着トナーが記載されてお
り、また特開昭48―75033号には粘り強い重合体
と軟質重合体のブロツク共重合体を用いた圧力定
着トナーが記載されている。 However, there are problems such as toner fixability and offset development to the pressure roller, and various research and developments are being carried out to improve the pressure fixing method. For example, Japanese Patent Publication No. 44-9880 describes a pressure fixing toner containing an aliphatic component and a thermoplastic resin;
No. 52-108134 describes a capsule-type pressure fixing toner containing a soft material in the core, and JP-A-48-75033 describes a block copolymer of a tenacious polymer and a soft polymer. Pressure-fixed toners using coalescence have been described.
しかし、製造が容易であり、加圧定着性能が充
分であり、加圧ローラーへのオフセツト現象を起
さず、繰り返し使用に対して現像性能、定着性能
が安定しており、キヤリヤー、金属スリーブ、感
光体表面への癒着を起さず、保存中に凝集、ケー
キ化しない保存安定性の良好である実用的な圧力
定着トナーは得られていない。 However, it is easy to manufacture, has sufficient pressure fixing performance, does not cause any offset phenomenon to the pressure roller, and has stable development performance and fixing performance even after repeated use. No practical pressure fixing toner has been obtained that does not adhere to the surface of a photoconductor, does not aggregate or form cakes during storage, and has good storage stability.
更に最近では本出願人が提案した特開昭54―
42141及び特開昭55―18656の如くトナー中に磁性
微粒子を含有せしめてキヤリヤー粒子を用いない
一成分系現像剤で静電潜像を現像する方法が行わ
れているが、この場合にはトナー結着樹脂は磁性
微粒子との分散性、密着性及びトナーの耐衝撃
性、流動性などが要求される。また、この一成分
系現像剤と現像スリーブローラーとの摩擦帯電に
よつて現像するとき、衝撃あるいは経時的使用等
により絶縁性物質が分離し、トリボ作用でスリー
ブローラーに付着して蓄積されて著しく耐久性に
劣るなど、一成分現像剤も多くの問題点を残して
いる。 More recently, the present applicant has proposed JP-A-54-
42141 and Japanese Patent Application Laid-open No. 18656/1983, there is a method of developing an electrostatic latent image with a one-component developer containing magnetic fine particles in the toner and using no carrier particles. The binder resin is required to have good dispersibility and adhesion with the magnetic fine particles, as well as impact resistance and fluidity of the toner. In addition, when developing by frictional charging between this one-component developer and the developing sleeve roller, insulating materials may separate due to impact or use over time, adhere to the sleeve roller due to triboelectric action, and accumulate, resulting in significant damage. One-component developers also have many problems, such as poor durability.
本発明は以上の如き要望を有利に解消したもの
であり、本発明の特徴はバインダー及び磁性粉よ
りなる磁性トナー100重量部に対してSnO2系微粉
末0.1〜10重量部を外添混合したことを特徴とす
る一成分系磁性現像剤に関するものであり、特に
前述の如き欠点を皆無にすることができ更に圧力
定着性の向上、環境安定性の向上等に有効な磁性
現像剤に関するものである。 The present invention advantageously satisfies the above-mentioned needs, and the feature of the present invention is that 0.1 to 10 parts by weight of SnO 2 -based fine powder is externally added to 100 parts by weight of a magnetic toner consisting of a binder and magnetic powder. The present invention relates to a one-component magnetic developer characterized by the following characteristics, and particularly relates to a magnetic developer which can completely eliminate the above-mentioned drawbacks and is effective in improving pressure fixing properties, improving environmental stability, etc. be.
圧力定着性の向上については磁性トナーは通常
バインダー磁性粉が含有されており、この磁性粉
の含有量が圧力定着性に大きく影響するものであ
る。即ち磁性粉含有量が多いと、トリボが発生せ
ず特開昭55―18656の如き現像方法では現像が不
可になり、また定着性が極めて不良であるために
磁性粉含有量は最少必要量に抑えることは必須で
ある。しかし乍ら少量にすると画像に“濃度ム
ラ”が生じる結果となる。これは現像スリーブ上
に形成するトナーの塗布膜厚が乱れるためであ
る。 Regarding the improvement of pressure fixability, magnetic toner usually contains a binder magnetic powder, and the content of this magnetic powder greatly influences the pressure fixability. In other words, if the magnetic powder content is large, triboelectricity will not occur and development will not be possible using the developing method of JP-A-18656, and the fixing properties will be extremely poor, so the magnetic powder content will be reduced to the minimum required amount. It is essential to suppress it. However, if the amount is small, "density unevenness" will occur in the image. This is because the thickness of the toner coating formed on the developing sleeve is disturbed.
即ち磁性粉含有量が極めて少ないとスリーブに
は、極めてトリボの高いトナーが吸引されもはや
磁場によるスリーブ上の搬送力が失なわれるため
である。従つてバインダーに対する磁性粉の含有
量は最適量が存在する。本発明はこのように磁性
粉含有量が少なくとも(言い換えるならば圧力定
着性が良好である)画像の濃度ムラを生じない効
果を表わすものとして、SnO2系の微粉末を見い
出したものである。 That is, if the magnetic powder content is extremely low, toner with extremely high triboelectricity will be attracted to the sleeve, and the magnetic field will no longer have the ability to convey the toner on the sleeve. Therefore, there is an optimum amount of magnetic powder contained in the binder. The present invention has thus discovered a SnO 2 -based fine powder that exhibits the effect of not causing density unevenness in images with at least a magnetic powder content (in other words, good pressure fixing properties).
また同時に環境安定性の向上が挙げられる。前
述の如きスリーブとの摩擦によるトナーは通常低
湿雰囲気ではトリボ量は高く高湿雰囲気では低
い。従つて低湿では画像濃度(Dmaxと略する)
が高いがトリボが高いので画像の“濃度ムラ”が
生じ、逆に高湿雰囲気ではDmaxの低下をもたら
すものである。 At the same time, environmental stability can be improved. Toner caused by friction with the sleeve as described above usually has a high tribo amount in a low humidity atmosphere and a low amount in a high humidity atmosphere. Therefore, at low humidity, the image density (abbreviated as Dmax)
However, since the triboelectricity is high, "density unevenness" occurs in the image, and conversely, in a high humidity atmosphere, Dmax decreases.
本発明の磁性現像剤は、このような欠点を皆無
にすることができたものであり、即ち本発明に於
て外添混合するSnO2系の微粉末はトリボコント
ロール剤として働きあらゆる雰囲気の環境で安定
化しているものと推察される。 The magnetic developer of the present invention can completely eliminate these drawbacks. In other words, the SnO 2 -based fine powder externally mixed in the present invention acts as a tribocontrol agent and can be used in any atmospheric environment. It is presumed that it has stabilized.
従つて外添混合するSnO2系微粉末の効果とし
て
1 環境安定性が向上され、低湿による画像の
“濃度ムラ”を生じない、且つ高湿においても
Dmaxの低下がない事が挙げられる。 Therefore, the effects of the externally added SnO 2 -based fine powder are as follows: 1. Environmental stability is improved, and "density unevenness" in images due to low humidity does not occur, and even in high humidity.
One example is that there is no decrease in Dmax.
2 磁性粉の含有量を少なくできるため圧力定着
性が向上する。2. Pressure fixing properties are improved because the content of magnetic powder can be reduced.
また本発明の特徴である磁性現像剤はトナーと
SnO2系微粉末を外添混合するところにある。 In addition, the magnetic developer, which is a feature of the present invention, is compatible with toner.
This is where SnO 2 -based fine powder is externally added and mixed.
SnO2系微粉末はトナーバインダーの中に添加
した(換言すると、内添する)場合本発明の特徴
が充分に発揮できない。何故ならば外添混合は内
添混合に比べ少量で充分な効果が発揮できるから
であり内添混合ではかえつて圧力定着性の向上を
阻害するものである。 When the SnO 2 -based fine powder is added into the toner binder (in other words, added internally), the features of the present invention cannot be fully exhibited. This is because mixing with external additions can achieve a sufficient effect with a smaller amount than mixing with internal additions, and mixing with internal additions actually hinders the improvement of pressure fixing properties.
また本発明においてはSnO2系としてSnO2―
TiO2系、SnO2―BaSO4系等も含むものとする。 In addition, in the present invention, SnO 2 -
It also includes TiO 2 series, SnO 2 -BaSO 4 series, etc.
SnO2系微粉末のの混合比についてはトナー100
重量部に対して0.1〜10重量部が適当で好ましく、
さらに0.3〜5重量部が良好である。即ち0.1部以
下では画像の“濃度ムラ”が発生し、10部以上で
は圧力定着性の向上が阻害されるばかりではな
く、高湿におけるDmax低下をもたらすものであ
る。 Regarding the mixing ratio of SnO 2 -based fine powder, toner 100
Appropriately and preferably 0.1 to 10 parts by weight,
Furthermore, 0.3 to 5 parts by weight is good. That is, if it is less than 0.1 part, "density unevenness" will occur in the image, and if it is more than 10 parts, not only will the improvement in pressure fixability be inhibited, but also a decrease in Dmax will occur at high humidity.
次に本発明の磁性現像剤について説明する。バ
インダーとして例えばワツクス、脂肪酸塩、ポリ
エチレン、ポリプロピレン弗素化樹脂、アイオノ
マー樹脂、テルペン樹脂、ロジン、フエノール変
性テルペン樹脂、ポリアミド、ポリエステル、低
分子ポリスチレン、マレイン酸性フエノール樹
脂、メチルビニルエーテル―無水マレイン酸樹
脂、ポリビニルピロリドン、塩素化パラフイン、
石油樹脂、ペンタエリスリトール樹脂等単独又は
混合して用いられる。また磁性粉はマグネタイ
ト、Znフエライト、C0マグネタイト等の金属酸
化物等従来より磁性材料として知られているもの
が用いられ、更に従来よりトナーに用いられてい
る公知の染顔料荷電制御剤を適当量添加してもよ
い。この磁性粉含有量はバインダー100重量部に
対して、20〜60重量部が適当であり、40〜60重量
部が好ましい。トナー化した後本発明の特徴であ
るSnO2系微粉末を外添する外に必要に応じてコ
ロイダルシリカ、酸化セリウム等流動性向上剤、
研磨剤を適宜混合してもよい。以下実施例により
具体的に述べる。 Next, the magnetic developer of the present invention will be explained. As a binder, for example, wax, fatty acid salt, polyethylene, polypropylene fluorinated resin, ionomer resin, terpene resin, rosin, phenol-modified terpene resin, polyamide, polyester, low molecular weight polystyrene, maleic acidic phenol resin, methyl vinyl ether-maleic anhydride resin, polyvinyl pyrrolidone, chlorinated paraffin,
Petroleum resin, pentaerythritol resin, etc. can be used alone or in combination. As the magnetic powder, conventionally known magnetic materials such as metal oxides such as magnetite, Zn ferrite, and C0 magnetite are used, and known dye/pigment charge control agents conventionally used in toners are also used. You may add a certain amount. The content of the magnetic powder is suitably 20 to 60 parts by weight, preferably 40 to 60 parts by weight, based on 100 parts by weight of the binder. After forming a toner, in addition to externally adding SnO 2 -based fine powder, which is a feature of the present invention, fluidity improvers such as colloidal silica and cerium oxide are added as necessary.
An abrasive may be mixed as appropriate. This will be described in detail below with reference to Examples.
実施例 1
ポリエチレンワツクス(ヘキスト社製商品名
PE130) 100重量部
磁性粉マグネタイト 50重量部
上記の混合物を150℃に加熱されたロールミル
を用いて10分間混練し冷却後ジエツトミルを用い
て粉砕した後5〜25μに分級しトナーを得た。次
にこのトナー100重量部に対して、疎水性コロイ
ダルシリカ(日本アエロジル(株)商品名R972)0.6
重量部、SnO2系微粉末(三菱金属製商品名T―
1)1.2重量部をコーヒーミル(柴田理化製小型
粉砕機)を用いて30秒間混合し現像剤を得た。次
に電子複写機(キヤノン製NP―120)に入れて
環境試験を行なつた。15℃10%及び35℃85%RH
の雰囲気でDmax低下は認められず画像に“濃度
ムラ”を生じなかつた。Example 1 Polyethylene wax (trade name manufactured by Hoechst)
PE130) 100 parts by weight Magnetic powder magnetite 50 parts by weight The above mixture was kneaded for 10 minutes using a roll mill heated to 150°C, cooled, pulverized using a jet mill, and classified into 5-25μ particles to obtain a toner. Next, 0.6 parts of hydrophobic colloidal silica (trade name R972, manufactured by Nippon Aerosil Co., Ltd.) is added to 100 parts by weight of this toner.
Part by weight, SnO 2 -based fine powder (Mitsubishi Metals product name T-
1) 1.2 parts by weight were mixed for 30 seconds using a coffee mill (small pulverizer manufactured by Shibata Rika) to obtain a developer. Next, I placed it in an electronic copying machine (Canon NP-120) and conducted an environmental test. 15℃10% and 35℃85%RH
No decrease in Dmax was observed in this atmosphere, and no "density unevenness" occurred in the image.
比較例として実施例1のSnO2系微粉末を外添
しない磁性現像剤を用いて実施例1と同様環境試
験を行なつたところ15℃10%で画像に“濃度のム
ラ”を生じた。 As a comparative example, an environmental test was conducted in the same manner as in Example 1 using a magnetic developer to which the SnO 2 -based fine powder of Example 1 was not externally added, and "density unevenness" occurred in the image at 15°C and 10%.
実施例 2
実施例1のSnO2微粉末をsnO2―BaSO4系(三
菱金属商品名T―10)微粉末0.8部に変える以外
実施例1と同様に処理を施こした。この磁性現像
剤を実施例1と同様にして環境試験を行なつたと
ころ15℃10%及び35℃85%RHの雰囲気でDmax
の低下及び画像の“濃度ムラ”の発生は認められ
なかつた。Example 2 The same treatment as in Example 1 was carried out except that the SnO 2 fine powder in Example 1 was replaced with 0.8 part of snO 2 -BaSO 4 type (Mitsubishi Metals trade name T-10) fine powder. This magnetic developer was subjected to an environmental test in the same manner as in Example 1, and the Dmax was found to be max.
No decrease in image quality or occurrence of "density unevenness" was observed.
実施例 3
実施例1のSnO2系微粉末をSnO2―TiO2系(三
菱金属製商品名W―10)1.0部に変える以外実施
例1と同様に処理を施こした。この磁性現像剤を
実施例1と同様環境試験を行なつたところ15℃10
%及び35℃85%RHの雰囲気でDmaxの低下及び
画像の“濃度ムラ”の発生は認められなかつた。Example 3 The same treatment as in Example 1 was carried out except that the SnO 2 -based fine powder in Example 1 was replaced with 1.0 part of SnO 2 -TiO 2 -based product (trade name W-10, manufactured by Mitsubishi Metals). This magnetic developer was subjected to an environmental test in the same manner as in Example 1.
% and in an atmosphere of 35°C and 85% RH, no decrease in Dmax or occurrence of "density unevenness" in images was observed.
実施例 4
スチレン―メタクリル酸ブチル―無水マレイ
ン酸樹脂(星光化学商品名ハイロスC―700)
100重量部
マグネタイト 60重量部
荷電制御剤 2重量部
上記の混合物を160℃に加熱されたロールミル
を用いて10分間混練し冷却後ジエツトミルを用い
て粉砕した後5〜25μに分級しトナーを得た。次
にこのトナー100重量部に対して疎水性コロイダ
ルシリカ(日本アエロジル社商品名R972)0.3重
量部SnO2系微粉末(三菱金属商品名T―1)2
重量部をコーヒーミルを用いて30秒間混合して現
像剤を得た。次に電子複写機(キヤノン製
NP200J)に入れて環境試験を行なつた。15℃10
%及び35℃85%RHの雰囲気でDmaxの低下は認
められず画像に“濃度のムラ”も生じなかつた。Example 4 Styrene-butyl methacrylate-maleic anhydride resin (Seiko Chemical product name Hyros C-700)
100 parts by weight Magnetite 60 parts by weight Charge control agent 2 parts by weight The above mixture was kneaded for 10 minutes using a roll mill heated to 160°C, cooled, pulverized using a jet mill, and classified into 5 to 25μ particles to obtain a toner. . Next, to 100 parts by weight of this toner, 0.3 parts by weight of hydrophobic colloidal silica (Japan Aerosil Co., Ltd. trade name R972) 0.3 parts by weight SnO 2 type fine powder (Mitsubishi Metals trade name T-1) 2
The weight parts were mixed for 30 seconds using a coffee mill to obtain a developer. Next, an electronic copying machine (manufactured by Canon)
NP200J) and conducted an environmental test. 15℃10
% and in an atmosphere of 35°C and 85% RH, no decrease in Dmax was observed, and no "density unevenness" occurred in the image.
比較例として実施例4のSnO2系微粉末を外添
しない磁性現像剤を用いて実施例4と同様環境試
験を行なつたところ15℃10%で画像に“濃度のム
ラ”を生じた。 As a comparative example, an environmental test was conducted in the same manner as in Example 4 using a magnetic developer to which the SnO 2 -based fine powder of Example 4 was not externally added, and "density unevenness" occurred in the image at 15°C and 10%.
Claims (1)
100重量部に対してSnO2系の微粉末0.1〜10重量
部を外添混合したことを特徴とする一成分系磁性
現像剤。1 Magnetic toner containing binder and magnetic powder
A one-component magnetic developer characterized in that 0.1 to 10 parts by weight of SnO 2 -based fine powder is externally added to 100 parts by weight.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP56038146A JPS57151952A (en) | 1981-03-17 | 1981-03-17 | Magnetic developer |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP56038146A JPS57151952A (en) | 1981-03-17 | 1981-03-17 | Magnetic developer |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS57151952A JPS57151952A (en) | 1982-09-20 |
JPS6339050B2 true JPS6339050B2 (en) | 1988-08-03 |
Family
ID=12517274
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP56038146A Granted JPS57151952A (en) | 1981-03-17 | 1981-03-17 | Magnetic developer |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS57151952A (en) |
Families Citing this family (9)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS6123160A (en) * | 1984-07-12 | 1986-01-31 | Fuji Xerox Co Ltd | One-component developer |
JPH0640223B2 (en) * | 1984-07-12 | 1994-05-25 | 富士ゼロックス株式会社 | One component developer |
JPS6159452A (en) * | 1984-08-31 | 1986-03-26 | Canon Inc | Positive-chargeable toner for electrophotography |
DE69028976T2 (en) * | 1989-12-08 | 1997-03-06 | Sharp Kk | Developer for electrophotography |
DE60111436T2 (en) | 2000-02-21 | 2006-05-11 | Canon K.K. | Developer, image production process and process cartridge |
DE60115737T2 (en) | 2000-02-21 | 2006-07-27 | Canon K.K. | Magnetic toner and image forming method using the same |
CA2337087C (en) | 2000-03-08 | 2006-06-06 | Canon Kabushiki Kaisha | Magnetic toner, process for production thereof, and image forming method, apparatus and process cartridge using the toner |
DE60126461T2 (en) | 2000-11-15 | 2007-10-25 | Canon K.K. | Image forming method and image forming apparatus |
JP3997065B2 (en) | 2001-08-20 | 2007-10-24 | キヤノン株式会社 | Process cartridge and image forming apparatus |
Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS51101535A (en) * | 1975-03-04 | 1976-09-08 | Toyo Ink Mfg Co | |
JPS53147541A (en) * | 1977-05-30 | 1978-12-22 | Ricoh Co Ltd | Electrophotographic toner |
-
1981
- 1981-03-17 JP JP56038146A patent/JPS57151952A/en active Granted
Patent Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS51101535A (en) * | 1975-03-04 | 1976-09-08 | Toyo Ink Mfg Co | |
JPS53147541A (en) * | 1977-05-30 | 1978-12-22 | Ricoh Co Ltd | Electrophotographic toner |
Also Published As
Publication number | Publication date |
---|---|
JPS57151952A (en) | 1982-09-20 |
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