JPH02223962A - Magnetite carrier particle and its production - Google Patents
Magnetite carrier particle and its productionInfo
- Publication number
- JPH02223962A JPH02223962A JP1044903A JP4490389A JPH02223962A JP H02223962 A JPH02223962 A JP H02223962A JP 1044903 A JP1044903 A JP 1044903A JP 4490389 A JP4490389 A JP 4490389A JP H02223962 A JPH02223962 A JP H02223962A
- Authority
- JP
- Japan
- Prior art keywords
- flame
- magnetite
- saturation magnetization
- particle size
- particles
- 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
- 239000002245 particle Substances 0.000 title claims abstract description 29
- 238000004519 manufacturing process Methods 0.000 title claims abstract description 18
- SZVJSHCCFOBDDC-UHFFFAOYSA-N iron(II,III) oxide Inorganic materials O=[Fe]O[Fe]O[Fe]=O SZVJSHCCFOBDDC-UHFFFAOYSA-N 0.000 title claims description 23
- UQSXHKLRYXJYBZ-UHFFFAOYSA-N Iron oxide Chemical compound [Fe]=O UQSXHKLRYXJYBZ-UHFFFAOYSA-N 0.000 claims abstract description 22
- 239000007789 gas Substances 0.000 claims abstract description 15
- 229910052760 oxygen Inorganic materials 0.000 claims abstract description 15
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims abstract description 14
- 239000001301 oxygen Substances 0.000 claims abstract description 14
- 230000005415 magnetization Effects 0.000 claims abstract description 12
- 239000012798 spherical particle Substances 0.000 claims abstract description 8
- 238000002485 combustion reaction Methods 0.000 claims abstract description 6
- 238000001816 cooling Methods 0.000 claims abstract description 5
- 239000011347 resin Substances 0.000 claims abstract description 3
- 229920005989 resin Polymers 0.000 claims abstract description 3
- 239000002994 raw material Substances 0.000 claims description 10
- 229910000831 Steel Inorganic materials 0.000 claims description 7
- 239000010959 steel Substances 0.000 claims description 7
- 239000011248 coating agent Substances 0.000 claims description 3
- 238000000576 coating method Methods 0.000 claims description 3
- 239000012535 impurity Substances 0.000 claims description 3
- 239000000463 material Substances 0.000 claims description 3
- 239000000203 mixture Substances 0.000 claims description 3
- 239000002253 acid Substances 0.000 claims 1
- 238000007885 magnetic separation Methods 0.000 claims 1
- 238000005406 washing Methods 0.000 claims 1
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 abstract description 15
- 239000000969 carrier Substances 0.000 abstract description 15
- 239000000843 powder Substances 0.000 abstract description 14
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 abstract description 7
- 229910052742 iron Inorganic materials 0.000 abstract description 4
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 abstract description 3
- 229910052757 nitrogen Inorganic materials 0.000 abstract description 2
- 238000000034 method Methods 0.000 description 19
- ATUOYWHBWRKTHZ-UHFFFAOYSA-N Propane Chemical compound CCC ATUOYWHBWRKTHZ-UHFFFAOYSA-N 0.000 description 18
- 239000007921 spray Substances 0.000 description 13
- 239000001294 propane Substances 0.000 description 9
- 229910000859 α-Fe Inorganic materials 0.000 description 7
- 238000011161 development Methods 0.000 description 6
- 238000005469 granulation Methods 0.000 description 5
- 230000003179 granulation Effects 0.000 description 5
- 238000001354 calcination Methods 0.000 description 4
- 238000010304 firing Methods 0.000 description 4
- 238000004898 kneading Methods 0.000 description 4
- 229910001873 dinitrogen Inorganic materials 0.000 description 3
- 238000010586 diagram Methods 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 238000000635 electron micrograph Methods 0.000 description 2
- 239000002737 fuel gas Substances 0.000 description 2
- 238000010438 heat treatment Methods 0.000 description 2
- 239000006247 magnetic powder Substances 0.000 description 2
- 238000005554 pickling Methods 0.000 description 2
- 239000002344 surface layer Substances 0.000 description 2
- BUGBHKTXTAQXES-UHFFFAOYSA-N Selenium Chemical compound [Se] BUGBHKTXTAQXES-UHFFFAOYSA-N 0.000 description 1
- ATRMIFNAYHCLJR-UHFFFAOYSA-N [O].CCC Chemical compound [O].CCC ATRMIFNAYHCLJR-UHFFFAOYSA-N 0.000 description 1
- HSFWRNGVRCDJHI-UHFFFAOYSA-N alpha-acetylene Natural products C#C HSFWRNGVRCDJHI-UHFFFAOYSA-N 0.000 description 1
- 238000010923 batch production Methods 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 239000002131 composite material Substances 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 239000013078 crystal Substances 0.000 description 1
- 230000007423 decrease 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
- 238000011156 evaluation Methods 0.000 description 1
- 239000010419 fine particle Substances 0.000 description 1
- 239000012530 fluid Substances 0.000 description 1
- 239000012634 fragment Substances 0.000 description 1
- 239000008187 granular material Substances 0.000 description 1
- 238000007689 inspection Methods 0.000 description 1
- 229910001337 iron nitride Inorganic materials 0.000 description 1
- 238000011031 large-scale manufacturing process Methods 0.000 description 1
- 239000010410 layer Substances 0.000 description 1
- 230000007774 longterm Effects 0.000 description 1
- 239000000155 melt Substances 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 239000011812 mixed powder Substances 0.000 description 1
- 229920000620 organic polymer Polymers 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 108091008695 photoreceptors Proteins 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- 238000007639 printing Methods 0.000 description 1
- 229910052711 selenium Inorganic materials 0.000 description 1
- 239000011669 selenium Substances 0.000 description 1
- 229920002545 silicone oil Polymers 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 238000012360 testing method Methods 0.000 description 1
- 238000012546 transfer Methods 0.000 description 1
Landscapes
- Developing Agents For Electrophotography (AREA)
- Compounds Of Iron (AREA)
Abstract
Description
【発明の詳細な説明】
〔産業上の利用分野〕
本発明は、電子写真法、静電記録法あるいは静電印刷法
等に使用される静電荷像現像剤用キャリアに関するもの
である。DETAILED DESCRIPTION OF THE INVENTION [Field of Industrial Application] The present invention relates to a carrier for an electrostatic image developer used in electrophotography, electrostatic recording, electrostatic printing, or the like.
電子複写の現像方法としては、湿式現像法と乾式現像法
に大別できるが、前者は有機溶媒をキャリアとし、て使
用するため、操作性・臭気公害等の問題が指摘され、現
在では米国特許Nα2786439号公明細書(195
a)に記載の乾式現像法である磁気ブラシ現像法が主流
となっている。この磁気ブラシ現像法では、可視像化す
るための現像剤として、磁性キャリアとトナーの混合粉
体である二成分系現像剤が使用され、キャリアとしては
現在、球形または不定形の鉄粉キャリア(例えば特公昭
47−19398号公報)、フェライトキャリア(例え
ば特公昭53−15040号公報)、複合キャリア(例
えば特開昭56−167150号公報)、マグネタイト
キャリア(例えば特公昭61−151551号公報)が
用いられ、さらにその表層を有機重合体で被覆すること
が行われている。Development methods for electronic copying can be roughly divided into wet development methods and dry development methods, but since the former uses an organic solvent as a carrier, problems such as operability and odor pollution have been pointed out, and it is currently covered by a U.S. patent. Nα2786439 Publication (195
The magnetic brush development method, which is the dry development method described in a), is the mainstream. In this magnetic brush development method, a two-component developer, which is a mixed powder of magnetic carrier and toner, is used as a developer for visualizing images, and the carrier is currently a spherical or irregularly shaped iron powder carrier. (for example, Japanese Patent Publication No. 47-19398), ferrite carriers (for example, Japanese Patent Publication No. 53-15040), composite carriers (for example, Japanese Patent Publication No. 167150/1982), magnetite carriers (for example, Japanese Patent Publication No. 151551/1982) is used, and its surface layer is further coated with an organic polymer.
しかし、鉄粉キャリアは嵩密度が大きく、また窒化鉄等
で表層を安定化しているため、長期間の使用に伴い、キ
ャリア表面の安定層が破壊したり、キャリア表面にトナ
ー被膜(俗に言うスペントトナー)が形成し、キャリア
粒子の抵抗が大幅に変化して摩擦帯電量が不安定となり
、その結果画像の濃度が低下したり、カブリが増大する
という欠点があった。However, iron powder carriers have a large bulk density and the surface layer is stabilized with iron nitride, etc., so with long-term use, the stable layer on the carrier surface may be destroyed or a toner film (commonly called (spent toner) is formed, the resistance of the carrier particles changes significantly, and the amount of triboelectric charging becomes unstable, resulting in a disadvantage that the density of the image decreases and fog increases.
そこで、鉄粉キャリアの代わりに内部まで組成が均一で
、表面も実用環境下で化学変化を受けず安定である、別
名r鉄フェライト1と呼ばれるマグネタイトキャリアが
開発された。マグネタイトキャリアは、飽和磁化がフェ
ライトキャリアより大きく鉄粉キャリアより小さいため
、鉄粉とフェライトの中間をいくキャリアとして注目さ
れている。Therefore, instead of the iron powder carrier, a magnetite carrier, also known as r-iron ferrite 1, was developed, which has a uniform composition even inside and whose surface is stable without undergoing chemical changes in a practical environment. Magnetite carriers have a saturation magnetization larger than that of ferrite carriers and smaller than that of iron powder carriers, so they are attracting attention as carriers that fall between iron powder and ferrite.
しかしながら、従来のマグネタイトキャリアは、第一に
酸化鉄粉を原料とした混練・造粒・焼成・解砕等に代表
されるフェライト製造法によって製造されるため、原料
を混練するための混練機、所要の球形に造粒するための
造粒機、フェライト反応を進めるための焼成炉、焼成中
に粒子が焼結するために生成したクラスターを解砕する
解砕機が必要であり、しかもこれらの工程がバッチ処理
のため大量生産には不向きであり、結果的に鉄粉キャリ
アに比較して製造コストが割高となる欠点があった。第
二に従来の造粒・焼成法では、上述した如く焼成中に粒
子が焼結しクラスターを生成するが、この現象は50n
以下の小粒径はど顕著であり、さらに後工程の解砕工程
では、50−以下の粒径範囲では破砕された破片と健全
なキャリアを分離することが事実上不可能なため、従来
法では50μ以下のキャリア製造は困難であった。第三
に解砕工程ではキャリアの基本仕様である球形粒子を破
砕してしまうので、歩留り低下と球状化率が悪化すると
いう難点があった。また、第四に原料が酸化鉄Cpet
os) 100%であるためフェライトキャリアのよう
に飽和磁化を任意に変化させることかできないという欠
点があった。However, since conventional magnetite carriers are first manufactured by a ferrite manufacturing method represented by kneading, granulation, firing, and crushing using iron oxide powder as a raw material, a kneader for kneading the raw materials, A granulator is required to granulate the particles into the desired spherical shape, a calcination furnace is required to advance the ferrite reaction, and a pulverizer is required to crush the clusters that are generated as the particles sinter during calcination. However, since it is a batch process, it is not suitable for mass production, and as a result, the production cost is higher than that of iron powder carriers. Second, in the conventional granulation and firing method, particles sinter and form clusters during firing as described above, but this phenomenon
In addition, in the subsequent crushing process, it is virtually impossible to separate crushed fragments from healthy carriers in the particle size range of 50- or less, so conventional methods Therefore, it was difficult to manufacture carriers with a thickness of 50 μm or less. Thirdly, in the crushing process, the spherical particles, which are the basic specifications of the carrier, are crushed, which has the disadvantage of lowering the yield and worsening the spheroidization rate. In addition, the fourth raw material is iron oxide Cpet.
os) 100%, so there was a drawback that the saturation magnetization could only be changed arbitrarily like a ferrite carrier.
従って、本発明の目的は、上述した問題点に対し、鉄鋼
製造工程の鋼材から発生するFeO−Fe、O。Therefore, an object of the present invention is to solve the above-mentioned problems by reducing FeO-Fe, O generated from steel materials during the steel manufacturing process.
を主組成とする酸化鉄を原料とした溶射火炎法を導入す
ることにより、従来の混練・造粒・焼成・解砕工程を必
要としない全く新しい連続製造方法を提供し、本製造方
法によって65n以下の粒径で、表面平滑度が高く高球
状化率で、磁気制御が可能なマグネタイトキャリア粒子
を提供することにある。By introducing a thermal spray flame method using iron oxide as a raw material, we have provided a completely new continuous manufacturing method that does not require the conventional kneading, granulation, calcination, and crushing steps. The object of the present invention is to provide magnetite carrier particles having the following particle diameters, high surface smoothness, high sphericity, and magnetic control.
本発明の前記課題は、第一に従来の酸化鉄粉原料に対し
て、鉄鋼製造工程、例えば加熱炉等で大量に発生するP
eOFe5Oaを主組成とする安価なミルスケールを原
料とすることで原料コストの低減を可能ならしめ、この
ミルスケール粉体の不純物を例えば酸洗処理等で除去し
た後乾燥し、所定粒度に粉砕後、輸送ガスと共に燃焼火
炎ガス中に投入・溶融し表面張力で球状粒子にするとい
う溶射火炎法を導入することにより、従来必要であった
混練・造粒・焼成・解砕工程を全く必要としない極めて
シンプルな工程で球形粒子を連続かつ大量・安価に生産
することを可能ならしめ、また第二に溶射火炎法を用い
ることにより小粒径範囲においても焼結クラスターが皆
無となることから、事前に原料を所定の粒径に粉砕する
ことによって65μm以下のキャリアを容易に製造なら
しめ、第三に解砕工程が不要であることから、表面平滑
度が高く高球状化率のキャリア粒子の製造を可能ならし
め、第四に溶射火炎処理中の火炎温度及び火炎中の酸素
濃度を制御することにより、飽和磁化の制御を可能なら
しめることによって解決することができる。The above-mentioned problems of the present invention are as follows: Firstly, compared to conventional iron oxide powder raw materials, a large amount of P is generated in the steel manufacturing process, for example, in a heating furnace.
It is possible to reduce the raw material cost by using inexpensive mill scale, which has eOFe5Oa as the main composition, and remove impurities from this mill scale powder by, for example, pickling treatment, dry it, and grind it to a predetermined particle size. By introducing a thermal spray flame method in which particles are put into a combustion flame gas together with a transport gas and melted into spherical particles using surface tension, the kneading, granulation, calcination, and crushing processes that were previously required are completely unnecessary. This makes it possible to produce spherical particles continuously, in large quantities, and at low cost using an extremely simple process.Secondly, by using the thermal spray flame method, there are no sintered clusters even in the small particle size range, so it is possible to produce spherical particles in advance. Firstly, carrier particles of 65 μm or less can be easily manufactured by crushing the raw materials to a predetermined particle size. Thirdly, since a crushing process is not required, carrier particles with high surface smoothness and high sphericity can be manufactured. Fourthly, by controlling the flame temperature and oxygen concentration in the flame during thermal spray flame treatment, the problem can be solved by making it possible to control the saturation magnetization.
本発明のマグネタイトキャリアは、一般に以下の方法で
得ることができる。The magnetite carrier of the present invention can generally be obtained by the following method.
第1図(a)は本発明に係わるマグネタイトキャリア粒
子の製造方法の実施装置を示す概略図、同図(b)は同
実施装置における溶射バーナーの正面図である。FIG. 1(a) is a schematic diagram showing an apparatus for implementing the method for manufacturing magnetite carrier particles according to the present invention, and FIG. 1(b) is a front view of a thermal spray burner in the same implementing apparatus.
第1図(b)に示す如く、溶射バーナー1の正面には、
二つの同心円周上に配列された火炎孔10の列の間に、
同じく同心円周上に配列された粉体孔11の列がサンド
ウィッチ状に配列されている。As shown in FIG. 1(b), on the front of the thermal spray burner 1,
Between the rows of flame holes 10 arranged on two concentric circles,
Similarly, rows of powder holes 11 arranged on concentric circles are arranged in a sandwich shape.
火炎孔10からは、酸素−プロパンによる火炎2が、粉
体孔11からは酸化鉄粉3が気体と共に噴出する。酸化
鉄粉は、ホッパー5に貯蔵されており、例えば窒素ガス
と共に粉体輸送管4を通じて溶射バーナー1に供給され
る。一方、支燃ガス及び燃料ガスとしては、酸素及びプ
ロパン(またはアセチレン)が、制御装置8を経由して
、酸素供給管6、プロパン供給管7を通じて溶射バーナ
ー1に供給される。酸素供給管6、プロパン供給管7は
溶射バーナー1の内部で合流しているので、酸素−プロ
パンの混合気体が生成し、この混合気体が火炎孔10よ
り噴出し、火炎2を形成する。A flame 2 of oxygen-propane is ejected from the flame hole 10, and iron oxide powder 3 is ejected together with gas from the powder hole 11. The iron oxide powder is stored in a hopper 5, and is supplied to the thermal spray burner 1 through the powder transport pipe 4 together with, for example, nitrogen gas. On the other hand, as combustion supporting gas and fuel gas, oxygen and propane (or acetylene) are supplied to the thermal spray burner 1 through the oxygen supply pipe 6 and the propane supply pipe 7 via the control device 8 . Since the oxygen supply pipe 6 and the propane supply pipe 7 meet inside the thermal spray burner 1, a mixed gas of oxygen and propane is generated, and this mixed gas is ejected from the flame hole 10 to form the flame 2.
形成した火炎2の熱により、窒素ガスと共に噴出した酸
化鉄粉3が溶融し、火炎2中に残存している酸素と反応
し、Fe、04に変化すると同時に表面張力によって球
状化する0球状化した磁性粉は冷却容器13内の水12
中に落下して急冷凝固され、この凝固した磁性粉を回収
後、酸洗し規格外キャリアを除去することによって、大
量のマグネタイトキャリアを製造することができる。更
に本製造方法では、ミルスケールの選択及び酸素/プロ
パン比を調節することによりFe、 PeO+FezO
a+FezO+等の生成割合を自由に制御することが可
能となる。Due to the heat of the formed flame 2, the iron oxide powder 3 ejected together with nitrogen gas melts, reacts with the oxygen remaining in the flame 2, changes to Fe, 04, and at the same time becomes spherical due to surface tension. The magnetic powder is poured into the water 12 in the cooling container 13.
A large quantity of magnetite carriers can be produced by collecting the solidified magnetic powder, which is then pickled to remove non-standard carriers. Furthermore, in this production method, by selecting the mill scale and adjusting the oxygen/propane ratio, Fe, PeO + FezO
It becomes possible to freely control the generation rate of a+FezO+, etc.
本発明を以下の実施例でさらに詳細に説明する。 The invention will be explained in further detail in the following examples.
実施例−1
鋳片加熱炉で発生したミルスケールを酸洗・乾燥後・乾
式粉砕機で100Al11以下の粒度に粉砕したものを
原料とし、燃料ガスにプロパン(15Nnf/hr)
、支燃ガスに酸素(75Nrrr/hr) 。Example-1 Mill scale generated in a slab heating furnace was pickled, dried, and ground to a particle size of 100Al11 or less using a dry grinder as a raw material, and propane (15Nnf/hr) was used as fuel gas.
, oxygen (75Nrrr/hr) as combustion supporting gas.
粉体輸送ガスに窒素(22N rd /hr)を使用し
、ミルスケール(304cg/hr)を第1図(a)に
示す装置で溶射火炎処理し、酸洗1分級1晶質検査を実
施し、所定のマグネタイトキャリアを製造した。Using nitrogen (22 N rd / hr) as the powder transport gas, mill scale (304 cg / hr) was subjected to thermal spray flame treatment with the equipment shown in Figure 1 (a), and pickling and 1 classification and 1 crystal quality inspection were carried out. , produced a given magnetite carrier.
製造したマグネタイトキャリアの特性値を第1表に示す
。第2図にマグネタイトキャリアの表面電子顕微鏡写真
を、第3図に同断面写真を示す。第2図から表面が極め
て平滑であり球状化率95%以上の球形粒子であること
が判る。また第3図から内部まで緻密で均一な組織が形
成されていることが理解できる。また、市販の現像機に
キャリア400ccを充填し、マグネットロールを12
0rp■でコピ−2万枚相当時間回転させた結果、キャ
リアの破壊は全く認められなかった。Table 1 shows the characteristic values of the produced magnetite carrier. FIG. 2 shows a surface electron micrograph of the magnetite carrier, and FIG. 3 shows a cross-sectional photograph of the same. From FIG. 2, it can be seen that the surface is extremely smooth and the particles are spherical with a sphericity of 95% or more. Furthermore, it can be seen from FIG. 3 that a dense and uniform structure is formed throughout the interior. In addition, a commercially available developing machine was filled with 400cc of carrier, and a magnetic roll of 12
As a result of rotating the carrier at 0 rpm for a time equivalent to 20,000 copies, no damage to the carrier was observed.
実施例−2
実施例−1と同様に作成した試料にシリコーンオイルを
転勤・流動コーティング装置を用いて1重量%表面被覆
した。本現像剤をセレン感光体を使用している複写機で
電子写真学会テストチャートを用いて画像評価を実施し
たところ、キャリア飛散もなく、解像度・べた黒・81
11性の良好な画像が得られた。Example 2 A sample prepared in the same manner as in Example 1 was coated with 1% by weight of silicone oil using a transfer/fluid coating device. When this developer was used in a copying machine that uses a selenium photoreceptor, image evaluation was carried out using the electrophotographic society test chart, and there was no carrier scattering, and the resolution was 81.
A good image with 11 characteristics was obtained.
実施例−3
実施例−1の条件をベースに、酸素/プロパン比を4〜
5の範囲で調節し、マグネタイトキャリアを製造した。Example-3 Based on the conditions of Example-1, the oxygen/propane ratio was changed from 4 to
A magnetite carrier was manufactured by adjusting the temperature within a range of 5.
結果を第2表に示す、この表から酸素/プロパン比の制
御によりマグネタイトキャリアの飽和磁化が制御可能で
あることが理解できる。The results are shown in Table 2. From this table, it can be understood that the saturation magnetization of the magnetite carrier can be controlled by controlling the oxygen/propane ratio.
第 2 表
〔発明の効果〕
以上説明したように、本発明によるマグネタイトキャリ
ア粒子は、鉄鋼製造工程の鋼材から発生する酸化鉄を原
料とし、不純物を酸洗し、乾燥し、100n以下の粒度
に粉砕後、輸送用ガスと共に燃焼火炎ガス中に投入し、
火炎中で溶融球状化すると共にガス中の酸素濃度を制御
することによりFe3O4生成比率を制御し、急冷し、
必要に応じて表面を樹脂で′被膜するという特徴を有し
た製法をとるため、保磁力500e以下、飽和磁化40
emu/ g以上、電気抵抗率104Ω・1以上、嵩密
度3g/cd以下である物性を有したマグネタイト組成
からなる上に、尚且つ球状化率95%以上で、表面平滑
度が高く、平均粒径が65μm以下の球形粒子で、飽和
磁化が40emu/g〜90emu/gの間制御可能で
あるという特徴を有し、次のような効果が得ら本る。Table 2 [Effects of the Invention] As explained above, the magnetite carrier particles according to the present invention are made from iron oxide generated from steel materials in the steel manufacturing process, pickled to remove impurities, dried, and reduced to a particle size of 100 nm or less. After crushing, it is put into combustion flame gas together with transportation gas,
The Fe3O4 production ratio is controlled by melting and spheroidizing in the flame and controlling the oxygen concentration in the gas, followed by rapid cooling.
Because the manufacturing method is characterized by coating the surface with resin as necessary, the coercive force is less than 500e and the saturation magnetization is 40.
It is composed of magnetite with physical properties of emu/g or more, electrical resistivity of 104 Ω・1 or more, and bulk density of 3 g/cd or less, and has a spheroidization rate of 95% or more, high surface smoothness, and an average grain size. It is a spherical particle with a diameter of 65 μm or less, and has the characteristics that the saturation magnetization can be controlled between 40 emu/g and 90 emu/g, and the following effects can be obtained.
(1)安価なミルスケールが使用でき、また混線・造粒
・焼成・解砕工程を全く必要としないシンプルな工程で
連続かつ大量に生産できるため、製造コストが安価とな
る。(1) Manufacturing costs are low because inexpensive mill scales can be used and continuous, large-scale production can be achieved through a simple process that does not require any cross-wire, granulation, firing, or crushing steps.
(2)65n以下の微細粒子であるため、解像度・緻密
性・べた黒均−性が向上した現像剤となる。(2) Since the particles are fine particles of 65 nm or less, the developer has improved resolution, density, and solid black uniformity.
(3ン 溶射火炎法を用いることにより、従来品より
表面平滑度が高く高球状化率のキャリア粒子が得られる
ため、現像剤トルクが低減し、スペントトナーの発生量
が減少し、長期間の現像性及び画像濃度の安定性に優れ
た現像剤となる。(3) By using the thermal spray flame method, carrier particles with higher surface smoothness and higher sphericity than conventional products can be obtained, which reduces developer torque, reduces the amount of spent toner, and reduces the amount of spent toner. It becomes a developer with excellent developability and stability of image density.
(4)飽和磁化の制御が可能なため、複写機現像エンジ
ンの設計自由度が大きくなる。(4) Since the saturation magnetization can be controlled, the degree of freedom in designing the copying machine developing engine is increased.
第1図(a)は本発明の実施装置の概略図、第1図(b
)は本発明の実施装置における溶射バーナーの正面図、
第2図は本発明によって得られたマグネタイトキャリア
粒子構造の表面電子顕微鏡写真図、第3図は同断面写真
図である。
l・・・溶射バーナー、2・・・火炎、3・・・酸化鉄
粉、4・・・粉体輸送管、5・・・ホッパー、6・・・
酸素供給管、7・・・プロパン供給管、8・・・制御装
置、9・・・窒素ガス供給管、10・・・火炎孔、11
・・・粉体孔、12・・・水、13・・・冷却容器。FIG. 1(a) is a schematic diagram of an implementation apparatus of the present invention, FIG. 1(b)
) is a front view of a thermal spray burner in an apparatus for implementing the present invention,
FIG. 2 is a surface electron micrograph of the magnetite carrier particle structure obtained by the present invention, and FIG. 3 is a cross-sectional photograph of the same. l... Thermal spray burner, 2... Flame, 3... Iron oxide powder, 4... Powder transport pipe, 5... Hopper, 6...
Oxygen supply pipe, 7... Propane supply pipe, 8... Control device, 9... Nitrogen gas supply pipe, 10... Flame hole, 11
...Powder hole, 12...Water, 13...Cooling container.
Claims (2)
上、電気抵抗率10^4Ω・cm以上、嵩密度3g/c
m^3以下のマグネタイト粒子において、球状化率が9
5%以上で、表面平滑度が高く、平均粒径が65μm以
下の球形粒子で、飽和磁化が40emu/g〜90em
u/gの間制御可能であることを特徴とするマグネタイ
トキャリア粒子。(1) Coercive force 500e or less, saturation magnetization 40emu/g or more, electrical resistivity 10^4Ω・cm or more, bulk density 3g/c
For magnetite particles of m^3 or less, the spheroidization rate is 9
5% or more, spherical particles with high surface smoothness, average particle size of 65 μm or less, and saturation magnetization of 40 emu/g to 90 em
Magnetite carrier particles characterized in that they are controllable between u/g.
3O_4を主組成とする酸化鉄原料を、輸送ガスと共に
燃焼火炎ガス中に投入し、火炎中で球状化すると共に、
急冷して製造するマグネタイトの製造方法において、原
料を事前に粉砕することで製品粒径を制御すること、火
炎温度及び火炎中の酸素濃度を制御することで生成する
Fe_3O_4比率を制御すること、酸洗または磁選に
よって不純物を除去すること、及び必要に応じて表面を
樹脂で被覆することを特徴とするマグネタイトキャリア
粒子の製造方法。(2) FeO-Fe_ generated from steel materials during the steel manufacturing process
An iron oxide raw material whose main composition is 3O_4 is put into combustion flame gas together with a transport gas, and while it is spheroidized in the flame,
In the manufacturing method of magnetite produced by rapid cooling, the product particle size is controlled by crushing the raw material in advance, the Fe_3O_4 ratio produced by controlling the flame temperature and the oxygen concentration in the flame, and the acid A method for producing magnetite carrier particles, which comprises removing impurities by washing or magnetic separation, and coating the surface with a resin if necessary.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP1044903A JPH02223962A (en) | 1989-02-23 | 1989-02-23 | Magnetite carrier particle and its production |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP1044903A JPH02223962A (en) | 1989-02-23 | 1989-02-23 | Magnetite carrier particle and its production |
Publications (1)
Publication Number | Publication Date |
---|---|
JPH02223962A true JPH02223962A (en) | 1990-09-06 |
Family
ID=12704431
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP1044903A Pending JPH02223962A (en) | 1989-02-23 | 1989-02-23 | Magnetite carrier particle and its production |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH02223962A (en) |
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---|---|---|---|---|
EP0580135A1 (en) * | 1992-07-22 | 1994-01-26 | Canon Kabushiki Kaisha | Carrier for use in electrophotography, two component-type developer and image forming method |
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JP2008249855A (en) * | 2007-03-29 | 2008-10-16 | Powdertech Co Ltd | Resin-coated ferrite carrier for electrophotographic developer and electrophotographic developer using the resin-coated ferrite carrier |
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JP2009180941A (en) * | 2008-01-31 | 2009-08-13 | Powdertech Co Ltd | Carrier core material for electrophotographic developer, carrier, and electrophotographic developer using the same (carrier) |
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-
1989
- 1989-02-23 JP JP1044903A patent/JPH02223962A/en active Pending
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EP0580135A1 (en) * | 1992-07-22 | 1994-01-26 | Canon Kabushiki Kaisha | Carrier for use in electrophotography, two component-type developer and image forming method |
EP0584555A1 (en) * | 1992-07-28 | 1994-03-02 | Canon Kabushiki Kaisha | Carrier for use in electrophotography, two component-type developer and image forming method |
EP1349014A2 (en) * | 2002-03-26 | 2003-10-01 | Powdertech Co. Ltd. | Carrier for electrophotographic developer and process of producing the same |
EP1349014A3 (en) * | 2002-03-26 | 2005-01-12 | Powdertech Co. Ltd. | Carrier for electrophotographic developer and process of producing the same |
US7824833B2 (en) | 2005-11-30 | 2010-11-02 | Powdertech Co., Ltd. | Resin-coated ferrite carrier for electrophotographic developer, its production method, and electrophotographic developer using the resin-coated ferrite carrier |
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US8067141B2 (en) | 2006-09-14 | 2011-11-29 | Ricoh Company, Ltd. | Electrographic carrier, developer, developing method, image forming apparatus, and process cartridge |
JP2008216339A (en) * | 2007-02-28 | 2008-09-18 | Powdertech Co Ltd | Core material of electrophotographic ferrite carrier and method of manufacturing resin coated ferrite carrier |
JP2008249855A (en) * | 2007-03-29 | 2008-10-16 | Powdertech Co Ltd | Resin-coated ferrite carrier for electrophotographic developer and electrophotographic developer using the resin-coated ferrite carrier |
US8247148B2 (en) * | 2007-03-29 | 2012-08-21 | Powdertech Co., Ltd. | Resin-coated ferrite carrier for electrophotographic developer and electrophotographic developer using the resin-coated ferrite carrier |
EP2133750A4 (en) * | 2007-03-30 | 2011-04-20 | Dowa Electronics Materials Co Ltd | Carrier core material for elctrophotographic developing agent, process for producing the core material, carrier for elctrophotographic developing agent, and electrophotographic developing agent. |
EP2133750A1 (en) * | 2007-03-30 | 2009-12-16 | DOWA Electronics Materials Co., Ltd. | Carrier core material for elctrophotographic developing agent, process for producing the core material, carrier for elctrophotographic developing agent, and electrophotographic developing agent. |
JP2009046384A (en) * | 2007-07-23 | 2009-03-05 | Hosokawa Funtai Gijutsu Kenkyusho:Kk | Metal oxide production device |
JP2009180941A (en) * | 2008-01-31 | 2009-08-13 | Powdertech Co Ltd | Carrier core material for electrophotographic developer, carrier, and electrophotographic developer using the same (carrier) |
JP2010083739A (en) * | 2008-10-02 | 2010-04-15 | Dowa Electronics Materials Co Ltd | Magnetic particle, carrier core material and manufacturing method of the same, and carrier and developer |
JP2012207817A (en) * | 2011-03-29 | 2012-10-25 | Taiyo Nippon Sanso Corp | Combustion burner |
WO2020104866A1 (en) * | 2018-11-23 | 2020-05-28 | Tata Steel Limited | A method of producing spherical iron powder and products thereof |
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