JP2009176960A - Magnetoplumbite type ferrite particle powder for bond magnet, method of manufacturing same, and resin composition, bond magnet, and magnet roll using magnetoplumbite type ferrite particle powder - Google Patents

Magnetoplumbite type ferrite particle powder for bond magnet, method of manufacturing same, and resin composition, bond magnet, and magnet roll using magnetoplumbite type ferrite particle powder Download PDF

Info

Publication number
JP2009176960A
JP2009176960A JP2008014219A JP2008014219A JP2009176960A JP 2009176960 A JP2009176960 A JP 2009176960A JP 2008014219 A JP2008014219 A JP 2008014219A JP 2008014219 A JP2008014219 A JP 2008014219A JP 2009176960 A JP2009176960 A JP 2009176960A
Authority
JP
Japan
Prior art keywords
particle powder
ferrite particle
magnet
type ferrite
powder
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Granted
Application number
JP2008014219A
Other languages
Japanese (ja)
Other versions
JP5267771B2 (en
Inventor
Yasushi Nishio
靖士 西尾
Yasuhiko Fujii
泰彦 藤井
Yosuke Koyama
陽介 小山
Tokuhiro Fukushina
徳浩 福品
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Toda Kogyo Corp
Original Assignee
Toda Kogyo Corp
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Toda Kogyo Corp filed Critical Toda Kogyo Corp
Priority to JP2008014219A priority Critical patent/JP5267771B2/en
Publication of JP2009176960A publication Critical patent/JP2009176960A/en
Application granted granted Critical
Publication of JP5267771B2 publication Critical patent/JP5267771B2/en
Expired - Fee Related legal-status Critical Current
Anticipated expiration legal-status Critical

Links

Landscapes

  • Compounds Of Iron (AREA)
  • Magnetic Ceramics (AREA)
  • Hard Magnetic Materials (AREA)
  • Manufacturing Cores, Coils, And Magnets (AREA)

Abstract

<P>PROBLEM TO BE SOLVED: To provide magnetoplumbite type ferrite particle powder for a bond magnet and a method of manufacturing the same, excellent in the magnetic characteristics and in the mechanical strength, and at the same time, capable of obtaining a bond magnet excellent in a coercive force iHc. <P>SOLUTION: Ferrite particle powder, in which the calcium content of magnetoplumbite type ferrite particle powder is 900 to 2,500 mg/kg as Ca, the pH is 10.5 to 12.5, and the average particle diameter is 1.0 to 3.0 μm, is obtained by blending and mixing raw material powder, temporarily baking the obtained raw material mixture power in the atmosphere at temperatures 900 to 1,250°C, and then, cracking and processing with water, adding Ca compound, and subjecting it to anneal heating processing in the atmosphere at temperatures 700 to 1,100°C. <P>COPYRIGHT: (C)2009,JPO&INPIT

Description

本発明は、磁気特性に優れ、機械的強度に優れると共に、保磁力iHcに優れたボンド磁石を得ることができるボンド磁石用マグネトプランバイト型フェライト粒子粉末及びその製造法に関するものであり、該マグネトプランバイト型フェライト粒子粉末を用いたボンド磁石用樹脂組成物、ボンド磁石並びにマグネットロールに関する。   The present invention relates to a magnetoplumbite-type ferrite particle powder for bonded magnets that can provide a bonded magnet with excellent magnetic properties, excellent mechanical strength, and excellent coercive force iHc, and a method for producing the same. The present invention relates to a resin composition for bonded magnets using a plumbite type ferrite particle powder, a bonded magnet, and a magnet roll.

周知の通り、ボンド磁石は、焼結磁石に比べ、軽量で、寸法精度が良く、複雑な形状も容易に量産化できる等の利点があるため、玩具用、事務用具用、音響機器用等の各種用途に広く使用されている。   As is well known, bonded magnets have advantages such as light weight, good dimensional accuracy, and easy mass production of complex shapes compared to sintered magnets. Widely used in various applications.

ボンド磁石に用いられる磁性粉末として、Nd−Fe−B系に代表される希土類磁石粉末やフェライト粒子粉末が知られている。希土類磁石粉末は高い磁気特性を有する反面、価格も高価であって、使用できる用途が制限されている。一方、フェライト粒子粉末は希土類磁石粉末に比べて磁気特性の面では劣っているが、安価であり化学的に安定であるため幅広い用途に用いられている。   As magnetic powders used in bond magnets, rare earth magnet powders and ferrite particle powders typified by Nd—Fe—B are known. Although rare earth magnet powder has high magnetic properties, it is also expensive and has limited uses. On the other hand, ferrite particle powder is inferior in terms of magnetic properties as compared with rare earth magnet powder, but it is inexpensive and chemically stable, so it is used in a wide range of applications.

ボンド磁石は、一般に、ゴム又はプラスチックス材料と磁性粉末とを混練した後、磁場中で成形するか、或いは機械的手段により成形することにより製造されている。   Bond magnets are generally manufactured by kneading a rubber or plastics material and magnetic powder and then molding them in a magnetic field or by mechanical means.

近年、各分野における用具や機器の小型化・軽量化に伴って、使用されるボンド磁石の高性能化とともに機械的強度に優れることが要求されている。   In recent years, along with the downsizing and weight reduction of tools and equipment in various fields, it is required that the bonded magnets used have high performance and excellent mechanical strength.

即ち、小型化された機器内のボンド磁石は過酷な条件で使用されることが多くなり、機械的な強度が要求される。例えば、コピー機、プリンター等では、マグネットロールが使用されているが、装置の長寿命化、及び、高速回転で用いられるため、機械的強度が高いことが強く要求されている。   That is, bond magnets in downsized equipment are often used under severe conditions, and mechanical strength is required. For example, although a magnet roll is used in a copying machine, a printer, and the like, it is strongly required to have a high mechanical strength because it is used for extending the life of the apparatus and rotating at high speed.

そこで、ボンド磁石に用いるマグネトプランバイト型フェライト粒子粉末においても、前記要求を満たすことができるフェライト粒子粉末が要求されている。   Therefore, there is a demand for a ferrite particle powder that can satisfy the above-described requirements also in the magnetoplumbite type ferrite particle powder used for the bond magnet.

これまで、ボンド磁石用フェライト粒子粉末について種々の改良が行われており、例えば、アルカリ金属化合物又はアルカリ土類金属化合物を融剤として用いてフェライト粒子粉末を製造する方法(特許文献1)、フェライト粒子粉末をアルカリ処理した後、カップリング剤で表面処理する方法(特許文献2)、フェライト仮焼粉末にCaO及びSiOを添加し焼結してフェライト磁石を得る方法(特許文献3)、フェライト粒子粉末の粒度分布を制御する方法(特許文献4)等が知られている。 So far, various improvements have been made to ferrite particle powders for bonded magnets. For example, a method of producing ferrite particle powder using an alkali metal compound or an alkaline earth metal compound as a flux (Patent Document 1), ferrite A method in which the particle powder is alkali-treated and then surface-treated with a coupling agent (Patent Document 2), a method in which CaO and SiO 2 are added to the calcined ferrite powder and sintered to obtain a ferrite magnet (Patent Document 3), ferrite A method for controlling the particle size distribution of the particle powder (Patent Document 4) is known.

特開昭55−145303号公報JP 55-145303 A 特開平5−41314号公報JP-A-5-41314 特開平5−275221号公報JP-A-5-275221 特開平4−224116号公報JP-A-4-224116

前記要求を満たすボンド磁石用マグネトプランバイト型フェライト粒子粉末は現在、最も要求されているところであるが、前記要求を十分に満たすものは未だ得られていない。   Magnetplumbite type ferrite particle powders for bonded magnets that satisfy the above requirements are currently in the most demanded state, but those that sufficiently satisfy the above requirements have not yet been obtained.

即ち、前出特許文献1乃至4に記載されたフェライト粒子粉末を用いたボンド磁石は、機械的強度に優れているとは言い難いものである。   That is, it is difficult to say that the bonded magnet using the ferrite particle powder described in the aforementioned Patent Documents 1 to 4 is excellent in mechanical strength.

そこで、本発明は、機械的強度に優れたボンド磁石が得られるボンド磁石用マグネトプランバイト型フェライト粒子粉末を得ることを技術的課題とする。   Then, this invention makes it a technical subject to obtain the magnetoplumbite type ferrite particle powder for bonded magnets from which the bonded magnet excellent in mechanical strength is obtained.

前記技術的課題は、次の通り本発明によって達成できる。   The technical problem can be achieved by the present invention as follows.

即ち、本発明は、マグネトプランバイト型フェライト粒子粉末のカルシウムの含有量が、Caとして900〜2500mg/kg(0.09〜0.25重量%)であり、pHが10.5〜12.5であり、平均粒径が1.0〜3.0μmであることを特徴とするボンド磁石用マグネトプランバイト型フェライト粒子粉末である(本発明1)。   That is, according to the present invention, the calcium content of the magnetoplumbite type ferrite particle powder is 900 to 2500 mg / kg (0.09 to 0.25 wt%) as Ca, and the pH is 10.5 to 12.5. And a magnetoplumbite type ferrite particle powder for bonded magnets, characterized in that the average particle size is 1.0 to 3.0 μm (Invention 1).

また、本発明は、原料粉末を配合・混合し、得られた原料混合粉末を大気中、900〜1250℃の温度範囲で仮焼した後、粉砕、水洗処理し、次いで、大気中、700〜1100℃の温度範囲でアニール加熱処理するボンド磁石用マグネトプランバイト型フェライト粒子粉末材料の製造方法において、前記仮焼以降のいずれかの工程におけるマグネトプランバイト型フェライト粒子粉末に対して、Ca化合物を前記フェライト粒子粉末に対して、1500〜30000mg/kg(0.15〜3.00重量%)添加することを特徴とする請求項1記載のボンド磁石用マグネトプランバイト型フェライト粒子粉末材料の製造方法である(本発明2)。   Moreover, this invention mix | blends and mixes raw material powder, After calcining the obtained raw material mixed powder in the temperature range of 900-1250 degreeC in air | atmosphere, it grind | pulverizes and water-washes, Then, in air | atmosphere, 700- In the manufacturing method of the magnetoplumbite type ferrite particle powder material for bonded magnet that is annealed and heated in a temperature range of 1100 ° C., a Ca compound is added to the magnetoplumbite type ferrite particle powder in any step after the calcination. The method for producing a magnetoplumbite-type ferrite particle powder material for bonded magnets according to claim 1, wherein 1500 to 30000 mg / kg (0.15 to 3.00 wt%) is added to the ferrite particle powder. (Invention 2).

また、本発明は、前記ボンド磁石用マグネトプランバイト型フェライト粒子粉末を用いた樹脂組成物である(本発明3)。   Moreover, this invention is a resin composition using the said magnetoplumbite-type ferrite particle powder for bonded magnets (this invention 3).

また、本発明は、前記ボンド磁石用マグネトプランバイト型フェライト粒子粉末を用いたボンド磁石である(本発明4)。   Moreover, this invention is a bonded magnet using the said magnetoplumbite type ferrite particle powder for bonded magnets (this invention 4).

また、本発明は、前記ボンド磁石用マグネトプランバイト型フェライト粒子粉末を用いたマグネットロールである(本発明5)。   Moreover, this invention is a magnet roll using the magnetoplumbite type ferrite particle powder for said bonded magnets (this invention 5).

本発明に係るボンド磁石用フェライト粒子粉末は、カルシウムをCa換算で900〜2500mg/kg(0.09〜0.25重量%)含有しており、その一部若しくは全部はフェライト粒子に化学吸着または化学結合しており、有機バインダー及び/又はシランカップリング剤と相互作用する磁性粉末であり、ボンド磁石用磁性粉末として好適である。   The ferrite particle powder for bonded magnet according to the present invention contains 900 to 2500 mg / kg (0.09 to 0.25% by weight) of calcium in terms of Ca. A magnetic powder that is chemically bonded and interacts with an organic binder and / or a silane coupling agent, and is suitable as a magnetic powder for a bond magnet.

本発明に係る樹脂組成物は、強度に優れた成形体が得られるので、ボンド磁石用として好適である。   The resin composition according to the present invention is suitable as a bonded magnet because a molded body having excellent strength can be obtained.

本発明に係るマグネットロールは、機械的強度に優れるので、好適である。   The magnet roll according to the present invention is suitable because it is excellent in mechanical strength.

以下、本発明を詳細に説明する。   Hereinafter, the present invention will be described in detail.

先ず、本発明に係るボンド磁石用マグネトプランバイト型フェライト粒子粉末(以下、「フェライト粒子粉末」という。)について説明する。   First, the magnetoplumbite type ferrite particle powder for bonded magnets according to the present invention (hereinafter referred to as “ferrite particle powder”) will be described.

本発明に係るフェライト粒子粉末の組成は、特に限定されるものではなく、Sr系フェライト粒子粉末、Ba系フェライト粒子粉末のいずれでもよい。また、La、Nd、Pr、Co、Zn等の異種元素を含有してもよい。また、等方性、異方性フェライトのどちらを使用しても良いが、マグネットロールなどの成型体表面の磁力を大きくするためには異方性フェライトを使用することが好ましい。   The composition of the ferrite particle powder according to the present invention is not particularly limited, and may be either Sr-based ferrite particle powder or Ba-based ferrite particle powder. Moreover, you may contain dissimilar elements, such as La, Nd, Pr, Co, Zn. Either isotropic or anisotropic ferrite may be used, but it is preferable to use anisotropic ferrite in order to increase the magnetic force on the surface of a molded body such as a magnet roll.

本発明に係るフェライト粒子粉末のカルシウム含有量は、Ca換算で900〜2500mg(0.09〜0.25重量%)である。Ca存在量が900mg/kg(0.09重量%)未満の場合、樹脂との反応性が低いため、機械的強度に優れた成形体が得られない。2500mg/kg(0.25重量%)を越える場合には、樹脂との反応性が高くなり過ぎることで、機械的強度に優れた成形体が得られない。好ましくは900〜2000mg/kg(0.09〜0.20重量%)である。   The calcium content of the ferrite particle powder according to the present invention is 900 to 2500 mg (0.09 to 0.25% by weight) in terms of Ca. When the Ca abundance is less than 900 mg / kg (0.09% by weight), since the reactivity with the resin is low, a molded article having excellent mechanical strength cannot be obtained. If it exceeds 2500 mg / kg (0.25% by weight), the reactivity with the resin becomes too high, so that a molded article having excellent mechanical strength cannot be obtained. It is preferably 900 to 2000 mg / kg (0.09 to 0.20% by weight).

本発明に係るフェライト粒子粉末の平均粒径は1.0〜3.0μmである。平均粒径が1.0〜3.0μmの範囲以外の場合には、ボンド磁石にする際に高充填ができなくなる為、高い磁気特性を有するボンド磁石を得ることが困難となる。より好ましくは1.0〜2.5μm、更により好ましくは1.0〜2.0μmである。   The average particle diameter of the ferrite particle powder according to the present invention is 1.0 to 3.0 μm. When the average particle size is outside the range of 1.0 to 3.0 μm, it becomes difficult to obtain a bonded magnet having high magnetic properties because high filling cannot be performed when the bonded magnet is formed. More preferably, it is 1.0-2.5 micrometers, More preferably, it is 1.0-2.0 micrometers.

本発明に係るフェライト粒子粉末の粉体pHは10.5〜12.5である。フェライト粒子粉末の粉体pHが前記範囲外の場合には、ボンド磁石にした際に、機械的強度に優れた成形体が得られない。より好ましくは10.5〜12.0である。   The powder pH of the ferrite particle powder according to the present invention is 10.5 to 12.5. When the powder pH of the ferrite particle powder is out of the above range, a molded body having excellent mechanical strength cannot be obtained when a bonded magnet is formed. More preferably, it is 10.5 to 12.0.

本発明に係るフェライト粒子粉末のBET比表面積値は1.0〜3.0m/gが好ましい。より好ましくは1.0〜2.5m/gである。 The BET specific surface area value of the ferrite particle powder according to the present invention is preferably 1.0 to 3.0 m 2 / g. More preferably, it is 1.0-2.5 m < 2 > / g.

本発明に係るフェライト粒子粉末の圧縮密度CDは、3000〜3500kg/m(3.00〜3.50g/cm)が好ましい。圧縮密度が3000kg/m(3.00g/cm)未満の場合には、充填性が低下するため、高い磁気特性を有するボンド磁石が得られない。圧縮密度が3500kg/m(3.50g/cm)を超える場合には、磁気特性などに問題はないが工業的には安定生産が困難である。フェライト粒子粉末の圧縮密度はより好ましくは3100〜3500kg/m(3.00〜3.50g/cm)であり、さらに好ましくは3200〜3450kg/m(3.00〜3.45g/cm)である。 The compression density CD of the ferrite particle powder according to the present invention is preferably 3000 to 3500 kg / m 3 (3.00 to 3.50 g / cm 3 ). When the compression density is less than 3000 kg / m 3 (3.00 g / cm 3 ), the filling property is lowered, so that a bonded magnet having high magnetic properties cannot be obtained. When the compression density exceeds 3500 kg / m 3 (3.50 g / cm 3 ), there is no problem in magnetic properties and the like, but industrially stable production is difficult. The compression density of the ferrite particle powder is more preferably 3100 to 3500 kg / m 3 (3.00 to 3.50 g / cm 3 ), and further preferably 3200 to 3450 kg / m 3 (3.00 to 3.45 g / cm 3 ). 3 ).

本発明に係るフェライト粒子粉末の飽和磁化値σは65.0〜73.0Am/kg(65.0〜73.0emu/g)が好ましく、保磁力iHcは、135〜279kA/m(1700〜3500Oe)が好ましい。 The saturation magnetization value σ s of the ferrite particle powder according to the present invention is preferably 65.0 to 73.0 Am 2 / kg (65.0 to 73.0 emu / g), and the coercive force iHc is 135 to 279 kA / m (1700). ~ 3500 Oe) is preferred.

次に、本発明に係るフェライト粒子粉末の製造法について述べる。   Next, a method for producing a ferrite particle powder according to the present invention will be described.

本発明に係るフェライト粒子粉末は、所定の配合割合で原料粉末を配合・混合して、得られた原料混合粉末を大気中、900〜1250℃の温度範囲で仮焼した後、粉砕、水洗処理し、次いで、大気中、700〜1100℃の温度範囲でアニール加熱処理する製造法において、Ca化合物を1500〜30000mg/kg(0.15〜3.00重量%)添加することにより得ることができる。尚、Ca化合物の添加は仮焼工程以降であればどの工程で行ってもよい。   The ferrite particle powder according to the present invention is prepared by mixing and mixing raw material powder at a predetermined mixing ratio, and calcining the obtained raw material mixed powder in the air at a temperature range of 900 to 1250 ° C. Then, in the production method of annealing and heating in the temperature range of 700 to 1100 ° C. in the atmosphere, it can be obtained by adding 1500 to 30000 mg / kg (0.15 to 3.00 wt%) of the Ca compound. . The Ca compound may be added in any process as long as it is after the calcination process.

原料粉末としては、マグネトプランバイト型フェライトを形成する各種金属の酸化物粉末、水酸化物粉末、炭酸塩粉末、硝酸塩粉末、硫酸塩粉末、塩化物粉末等の中から適宜選択すればよい。なお、仮焼時における反応性の向上を考慮すれば、粒子径は2.0μm以下が好ましい。   The raw material powder may be appropriately selected from oxide powders, hydroxide powders, carbonate powders, nitrate powders, sulfate powders, chloride powders and the like of various metals forming magnetoplumbite-type ferrite. In consideration of improvement in reactivity during calcination, the particle size is preferably 2.0 μm or less.

Ca化合物としては、Ca(OH)、CaO、CaCOなど特に制限するものではないが、反応性に優れるCa(OH)、CaOが好ましく、Ca(OH)がより好ましい。 The Ca compound is not particularly limited, such as Ca (OH) 2 , CaO, CaCO 3 , but Ca (OH) 2 and CaO excellent in reactivity are preferable, and Ca (OH) 2 is more preferable.

また、本発明においては、原料混合粉末に融剤を添加して仮焼することが好ましい。融剤としては、各種融剤を用いることができ、例えば、SrCl・2HO、CaCl・2HO、MgCl、KCl、NaCl、BaCl・2HO及びNaである。添加量は、原料混合粉末100重量部に対してそれぞれ1〜10重量部が好ましい。より好ましくは1〜8重量部である。 Moreover, in this invention, it is preferable to calcine by adding a flux to raw material mixed powder. As the flux, various fluxes can be used, for example, SrCl 2 · 2H 2 O, CaCl 2 · 2H 2 O, MgCl 2 , KCl, NaCl, BaCl 2 · 2H 2 O and Na 2 B 4 O 7. It is. The addition amount is preferably 1 to 10 parts by weight per 100 parts by weight of the raw material mixed powder. More preferably, it is 1 to 8 parts by weight.

また、本発明においてはBiを原料混合粉末又は仮焼後の粉砕粉末に添加・混合してもよい。 In the present invention, Bi 2 O 3 may be added to and mixed with the raw material mixed powder or the pulverized powder after calcination.

なお、本発明においては、粒度分布制御の点から、大粒子と小粒子とを混合してもよい。   In the present invention, large particles and small particles may be mixed from the viewpoint of particle size distribution control.

Ca化合物の添加量は、フェライト粒子粉末に対して1500〜30000mg/kg(0.15〜3.00重量%)である。Ca添加量が1500mg(0.15重量%)未満の場合、得られるフェライト粒子粉末を使用した成形体は、樹脂との反応性が低いため、機械的強度が十分とは言い難い。30000mg(3.00重量%)を越える場合には、樹脂との反応性が高くなり過ぎることで、機械的強度に優れた成形体が得られない。より好ましくは3000〜20000mg/kg(0.30〜2.00重量%)である。   The addition amount of Ca compound is 1500-30000 mg / kg (0.15-3.00 weight%) with respect to ferrite particle powder. When the amount of Ca added is less than 1500 mg (0.15% by weight), the molded body using the obtained ferrite particle powder has a low reactivity with the resin, so it is difficult to say that the mechanical strength is sufficient. When it exceeds 30000 mg (3.00% by weight), the reactivity with the resin becomes too high, so that a molded article having excellent mechanical strength cannot be obtained. More preferably, it is 3000-20000 mg / kg (0.30-2.00 weight%).

次に、本発明に係るフェライト粒子粉末を用いたボンド磁石用組成物について述べる。   Next, the composition for bonded magnets using the ferrite particle powder according to the present invention will be described.

本発明に係るボンド磁石組成物は、ボンド磁石用組成物中における前記フェライト粒子粉末の割合が70〜95重量部と有機バインダー成分およびシランカップリング剤成分を総量で5〜30重量部になるように、混合混練したものである。   In the bonded magnet composition according to the present invention, the ratio of the ferrite particle powder in the bonded magnet composition is 70 to 95 parts by weight, and the total amount of the organic binder component and the silane coupling agent component is 5 to 30 parts by weight. And kneaded.

有機バインダーとしては従来のボンド磁石に使用されているものであれば特に制限はなく、ゴム、塩化ビニル樹脂、エチレン−酢酸ビニル共重合体樹脂、エチレンーエチルアクリレート共重合樹脂、PPS樹脂、ポリアミド(ナイロン)樹脂、ポリアミドエラストマー、重合脂肪酸系ポリアミド等から用途に応じて選択・使用できる。また、必要に応じてステアリン酸亜鉛、ステアリン酸カルシウム等の公知の離型剤を添加することができる。   The organic binder is not particularly limited as long as it is used in conventional bonded magnets. Rubber, vinyl chloride resin, ethylene-vinyl acetate copolymer resin, ethylene-ethyl acrylate copolymer resin, PPS resin, polyamide ( Nylon) resin, polyamide elastomer, polymerized fatty acid polyamide and the like can be selected and used according to the application. Moreover, well-known mold release agents, such as a zinc stearate and a calcium stearate, can be added as needed.

本発明に係るボンド磁石の残留磁束密度Brは230mT(2300G)以上が好ましく、より好ましくは235mT(2350G)以上である。保磁力iHcは119〜279kA/m(1500〜3500Oe)が好ましく、より好ましくは127〜259kA/m(1600〜3250Oe)である。最大エネルギー積BHmaxは10.3kJ/m(1.30MGOe)以上が好ましく、より好ましくは10.7kJ/m(1.35MGOe)以上である。 The residual magnetic flux density Br of the bonded magnet according to the present invention is preferably 230 mT (2300 G) or more, more preferably 235 mT (2350 G) or more. The coercive force iHc is preferably 119 to 279 kA / m (1500 to 3500 Oe), more preferably 127 to 259 kA / m (1600 to 3250 Oe). The maximum energy product BHmax is preferably 10.3 kJ / m 3 (1.30 MGOe) or more, more preferably 10.7 kJ / m 3 (1.35 MGOe) or more.

次に、本発明に係るフェライト粒子粉末、樹脂バインダー、シランカップリング剤を用いたボンド磁石用組成物の製造法について述べる。   Next, a method for producing a bonded magnet composition using the ferrite particle powder, resin binder, and silane coupling agent according to the present invention will be described.

本発明に係るボンド磁石は、周知のボンド磁石の製造法によって得ることができ、例えば、本発明に係るフェライト粒子粉末と前記結合樹脂とを混合した後、混練押出機などを用いて溶融混練し、混練物を粒状、ペレット状に粉砕または切断することによって得られる。   The bond magnet according to the present invention can be obtained by a known bond magnet manufacturing method. For example, the ferrite particle powder according to the present invention and the binding resin are mixed and then melt-kneaded using a kneading extruder or the like. It can be obtained by crushing or cutting the kneaded product into a granular or pellet form.

次に、マグネットロールに関して記載する。   Next, it describes about a magnet roll.

マグネットロールは、ボンド磁石用フェライト磁性粉と有機バインダー成分等を予め混合、および/または、それらを混合後に溶融混練まで実施してペレット状に粉砕または切断してボンド磁石組成物として、溶融状態で金型のキャビティーの磁場中に射出し、磁性粉を配向させる所謂磁場射出成型において周面上に複数の磁極を有する柱状の本体部と、この本体部の両端面に設けられた軸部とを一体して成型することによって得た。なお、成型体は直径13.6mmで長さが220mmの胴体部と直径5mm(円心は直径13.6mmの胴体部と同一)の軸部を両端に有する一体成型したものである。   The magnet roll is prepared by mixing ferrite magnetic powder for bonded magnet and organic binder component in advance, and / or carrying out the process up to melt kneading after mixing them, and pulverizing or cutting them into a pellet to obtain a bonded magnet composition in a molten state. Columnar body portions having a plurality of magnetic poles on the peripheral surface in so-called magnetic field injection molding that is injected into the magnetic field of the mold cavity and orients the magnetic powder, and shaft portions provided on both end faces of the body portion; Was obtained by integrally molding. The molded body is integrally molded having a body portion having a diameter of 13.6 mm and a length of 220 mm and a shaft portion having a diameter of 5 mm (the center is the same as the body portion having a diameter of 13.6 mm) at both ends.

<作用>
本発明に係るフェライト粒子粉末がCaを含有することで、該フェライト粒子粉末を含んだ成型体の機械的強度が優れることについては未だ明らかではないが、本発明者は次のように推定している。
<Action>
Although it is not yet clear that the ferrite particles powder according to the present invention contains Ca and the mechanical strength of the molded body containing the ferrite particles powder is excellent, the present inventor presumes as follows: Yes.

本発明に係るボンド磁石用フェライト粒子粉末は、Caを含有することで有機バインダー成分とシランカップリング剤の反応性が向上して、フェライト粒子粉末、有機バインダー及びシランカップリング剤の3成分の相溶性が相乗的に向上したため、フェライト粒子粉末及び有機バインダーが強固に結合したためと推定している。   The ferrite particle powder for bonded magnet according to the present invention improves the reactivity of the organic binder component and the silane coupling agent by containing Ca, and the three-component phase of the ferrite particle powder, the organic binder and the silane coupling agent. It is presumed that the ferrite particles powder and the organic binder were firmly bonded because the solubility was synergistically improved.

本発明の代表的な実施の形態は次の通りである。   A typical embodiment of the present invention is as follows.

本発明に係るフェライト粒子粉末の平均粒径は、「粉体比表面積測定装置SS−100」(島津製作所(株)製)を用いて測定した。   The average particle size of the ferrite particle powder according to the present invention was measured using “Powder Specific Surface Area Measuring Device SS-100” (manufactured by Shimadzu Corporation).

本発明に係るフェライト粒子粉末のBET比表面積は、「4検体全自動比表面積測定装置4ソーブU2」(湯浅アイオニクス(株)製)を用いて測定した。   The BET specific surface area of the ferrite particle powder according to the present invention was measured using “4 specimen fully automatic specific surface area measuring device 4 Sorb U2” (manufactured by Yuasa Ionics Co., Ltd.).

本発明に係るフェライト粒子粉末の圧縮密度には、粒子粉末を1t/cmの圧力で圧縮したときの密度を採用した。 As the compression density of the ferrite particle powder according to the present invention, the density when the particle powder was compressed at a pressure of 1 t / cm 2 was adopted.

本発明に係るフェライト粒子粉末の粉体pHは、JIS K5101−17−1に準拠して「ガラス電極式水素イオン濃度計M8E」((株)堀場製作所製)を用いて測定した。   The powder pH of the ferrite particle powder according to the present invention was measured using a “glass electrode type hydrogen ion concentration meter M8E” (manufactured by Horiba, Ltd.) in accordance with JIS K5101-17-1.

ボンド磁石組成物の成型密度は、ボンド磁石組成物を25mmφ、10.5mmの高さの金型内で溶融状態にして成型したコアを「電子比重計EW−120SG」((株)安田精機製作所製)で測定して求めた。   The molding density of the bonded magnet composition is such that the core formed by melting the bonded magnet composition in a mold with a diameter of 25 mmφ and 10.5 mm is “electronic hydrometer EW-120SG” (Yasuda Seiki Seisakusho Co., Ltd.) Measured).

ボンド磁石組成物の磁気特性(残留磁束密度Br、保磁力iHc、保磁力bHc、最大エネルギー積BHmax)は、ボンド磁石組成物を25mmφ、10.5mmの高さの金型内で溶融状態として、4kOeで磁場配向した後、「直流磁化特性自動記録装置3257」(横川北辰電気(株)製)を用いて14kOeの磁界中で測定して求めた。   The magnetic properties (residual magnetic flux density Br, coercive force iHc, coercive force bHc, maximum energy product BHmax) of the bonded magnet composition are as follows. The bonded magnet composition is melted in a mold having a height of 25 mmφ and 10.5 mm. After magnetic field orientation at 4 kOe, measurement was performed in a magnetic field of 14 kOe using a “DC magnetization characteristic automatic recording device 3257” (manufactured by Yokogawa Hokushin Electric Co., Ltd.).

ボンド磁石組成物を用いた射出成型は、(株)日本製鋼所製の射出成形機110ELII型を用いて、直径13.6mmで長さが220mmの胴体部と直径5mm(円心は直径13.6mmの胴体部と同一)の軸部を両端に有する一体成型として、射出成型機内で胴体部にS1、S2、N1、N2のように4極に着磁した後、冷却してマグネットロールとして取り出した。
また、金型の設定温度は100℃として、マグネットロール表面温度も100℃近傍まで冷却した。
The injection molding using the bonded magnet composition was performed using an injection molding machine 110ELII manufactured by Nippon Steel Co., Ltd., and a body portion having a diameter of 13.6 mm and a length of 220 mm and a diameter of 5 mm (the center of the diameter is 13. (Same as 6mm body part) Shaft part is integrally molded at both ends, and the body part is magnetized to 4 poles like S1, S2, N1, N2 in the injection molding machine, then cooled and taken out as a magnet roll It was.
The set temperature of the mold was 100 ° C., and the surface temperature of the magnet roll was also cooled to near 100 ° C.

マグネットロールの機械的強度は、大気中で24時間放置した後、マグネットロール本体部の3点曲げ強度をオートグラフAG−Iシリーズ」((株)島津製作所製)で測定して曲げ強度として求めた。   The mechanical strength of the magnet roll is determined as the bending strength after being left in the atmosphere for 24 hours and then measuring the three-point bending strength of the magnet roll body with the Autograph AG-I series (manufactured by Shimadzu Corporation). It was.

実施例1
<フェライト粒子粉末の製造>
粉末状のα−Fe、SrCOを組成がSrO・nFe[n=6.3]となるように秤量して、湿式アトライターで30分間混合した後、濾過、乾燥した(第一湿式混合粉砕工程)。
得られた混合粉末にSrCl及びNaの混合水溶液を添加してよく混合した後、造粒した。このとき、SrCl及びNaの添加量は、上記原料混合粉末100重量部に対してそれぞれ3重量部、0.5重量部とした。得られた造粒物を大気中1200℃で2時間仮焼した(仮焼工程)。
得られた仮焼物を粗粉砕した後に、湿式アトライターで30分間粉砕し、水洗、濾過、脱水した。その後、Ca(OH)を添加し、湿式アトライターで5分間混合粉砕し、濾過、脱水した(第二湿式混合粉砕工程)。このとき、Ca(OH)の添加量は、上記粗粉砕物100重量部に対して0.5重量部とした。
その後、更に、振動ミルで30分間粉砕した(乾式混合粉砕工程)。得られた粉砕物を大気中900℃で1.5時間アニール加熱処理し(熱処理工程)、次いでヘンシェルミキサーにて10分間均一混合した(均一混合工程)。
Example 1
<Manufacture of ferrite particle powder>
Powdered α-Fe 2 O 3 and SrCO 3 were weighed so that the composition was SrO · nFe 2 O 3 [n = 6.3], mixed for 30 minutes with a wet attritor, filtered and dried. (First wet mixing and grinding step).
A mixed aqueous solution of SrCl 2 and Na 2 B 4 O 7 was added to the obtained mixed powder and mixed well, followed by granulation. At this time, the addition amounts of SrCl 2 and Na 2 B 4 O 7 were 3 parts by weight and 0.5 parts by weight, respectively, with respect to 100 parts by weight of the raw material mixed powder. The obtained granulated material was calcined in the atmosphere at 1200 ° C. for 2 hours (calcination step).
The obtained calcined product was roughly pulverized and then pulverized with a wet attritor for 30 minutes, washed with water, filtered and dehydrated. Thereafter, Ca (OH) 2 was added, mixed and pulverized with a wet attritor for 5 minutes, filtered and dehydrated (second wet mixed pulverization step). At this time, the addition amount of Ca (OH) 2 was 0.5 parts by weight with respect to 100 parts by weight of the coarsely pulverized product.
Thereafter, the mixture was further pulverized with a vibration mill for 30 minutes (dry mixing and pulverizing step). The obtained pulverized product was annealed and heated in the atmosphere at 900 ° C. for 1.5 hours (heat treatment step), and then uniformly mixed with a Henschel mixer for 10 minutes (uniform mixing step).

得られたフェライト粒子粉末の保磁力iHcは214.1kA/m(2690Oe)であった。平均粒径Psは1.57μmであり、BET比表面積は1.30m/gであった。圧縮密度CDは3420kg/m(3.42g/cm)であった。pHは10.8であった。また、Ca含有量は1000mg/kg(0.10wt%)であった。 The obtained ferrite particle powder had a coercive force iHc of 214.1 kA / m (2690 Oe). The average particle size Ps was 1.57 μm, and the BET specific surface area was 1.30 m 2 / g. The compression density CD was 3420 kg / m 3 (3.42 g / cm 3 ). The pH was 10.8. Moreover, Ca content was 1000 mg / kg (0.10 wt%).

実施例2〜5、比較例1〜4:
組成、仮焼時間、Ca化合物の種類、添加量及び添加時期、粉砕時間などを種々変化させた以外は、前記実施例1と同様にしてフェライト粒子粉末を作成した。作成したフェライト粒子粉末の特性を表1に示す。
Examples 2-5, Comparative Examples 1-4:
Ferrite particle powder was prepared in the same manner as in Example 1 except that the composition, calcining time, type of Ca compound, addition amount and addition time, pulverization time, and the like were variously changed. Table 1 shows the properties of the prepared ferrite particle powder.

実施例6
<ボンド磁石用組成物の製造>
得られたフェライト粒子粉末を乾式混合機に25000g入れ、シランカップリング剤をフェライトに対して0.6重量部添加して1時間均一になるまで混合し、さらに、6−ナイロン樹脂を2507g投入した後、さらに1時間混合してボンド磁石用組成物用の混合物を用意した。
Example 6
<Manufacture of composition for bonded magnet>
25,000 g of the obtained ferrite particle powder was put in a dry mixer, 0.6 parts by weight of a silane coupling agent was added to ferrite and mixed until uniform for 1 hour, and 2507 g of 6-nylon resin was added. Then, it further mixed for 1 hour and prepared the mixture for the composition for bond magnets.

得られたボンド磁石組成物用の混合物を2軸の混練機に定量フィードして6−ナイロンが溶融する温度において混練して、混練物をストランド状にして取り出し2mmφ×3mmの大きさのペレット状に切断してボンド磁石用組成物を得た。   The obtained mixture for the bonded magnet composition is quantitatively fed to a biaxial kneader and kneaded at a temperature at which 6-nylon is melted. The kneaded product is taken out into a strand shape and taken out as a pellet having a size of 2 mmφ × 3 mm. The composition for bonded magnets was obtained by cutting.

このボンド磁石の残留磁束密度Brは294mT(2940G)であり、保磁力iHcは208.5kA/m(2620Oe)であり、最大エネルギー積BHmaxは16.7kJ/m(2.10MGOe)であった。 The bond magnet had a residual magnetic flux density Br of 294 mT (2940 G), a coercive force iHc of 208.5 kA / m (2620 Oe), and a maximum energy product BHmax of 16.7 kJ / m 3 (2.10 MGOe). .

<マグネットロールの成形>
得られたボンド磁石用樹脂組成物を100℃で8時間乾燥した後、射出成型機においてボンド磁石用樹脂組成物を290℃で溶融し、射出時間1.8秒で100℃に設定された金型に射出成形して、直径13.6mmで長さが220mmの胴体部と直径5.0mm(軸心は直径13.6mmの胴体部と同一)の軸部を両端に有する一体成型マグネットロールを用意した。
<Molding of magnet roll>
The obtained bonded magnet resin composition was dried at 100 ° C. for 8 hours, and then the bonded magnet resin composition was melted at 290 ° C. in an injection molding machine, and the injection time was set to 100 ° C. in 1.8 seconds. An integrally molded magnet roll having a diameter of 13.6 mm and a length of 220 mm and a shaft having a diameter of 5.0 mm (the axis is the same as that of the diameter of 13.6 mm) are formed at both ends. Prepared.

得られた一体成型マグネットロールの曲げ強度は、752Nであった。   The bending strength of the obtained integrally molded magnet roll was 752N.

実施例7〜10、比較例5〜8:
<ボンド磁石用組成物の製造>
各種フェライト粒子粉末と6−ナイロン樹脂、シランカップリング剤からなるボンド磁石用樹脂組成物を前記実施例6と同様にして作成した。
Examples 7-10, Comparative Examples 5-8:
<Manufacture of composition for bonded magnet>
Resin compositions for bonded magnets comprising various ferrite particle powders, 6-nylon resin, and silane coupling agent were prepared in the same manner as in Example 6.

ボンド磁石用樹脂組成物の特性を表2に示す。   Table 2 shows the properties of the resin composition for bonded magnets.

<マグネットロールの成形>
種々のボンド磁石用樹脂組成物を用いて、前記実施例6と同様にしてマグネットロールを作成した。マグネットロールの特性を表2に示す。
<Molding of magnet roll>
Magnet rolls were prepared in the same manner as in Example 6 using various resin compositions for bonded magnets. Table 2 shows the characteristics of the magnet roll.

Figure 2009176960
Figure 2009176960

Figure 2009176960
Figure 2009176960

本発明に係るフェライト粒子粉末を用いて製造したボンド磁石は曲げ強度に優れるので、ボンド磁石、特にマグネットロール用のフェライト粒子粉末として好適である。
Since the bonded magnet manufactured using the ferrite particle powder according to the present invention is excellent in bending strength, it is suitable as a bonded magnet, particularly as a ferrite particle powder for a magnet roll.

Claims (5)

マグネトプランバイト型フェライト粒子粉末のカルシウムの含有量が、Caとして900〜2500mg/kg(0.09〜0.25重量%)であり、pHが10.5〜12.5であり、平均粒径が1.0〜3.0μmであることを特徴とするボンド磁石用マグネトプランバイト型フェライト粒子粉末。 The magnetoplumbite type ferrite particle powder has a calcium content of 900 to 2500 mg / kg (0.09 to 0.25 wt%) as Ca, a pH of 10.5 to 12.5, and an average particle size. A magnetoplumbite type ferrite particle powder for bonded magnets, characterized in that is 1.0 to 3.0 μm. 原料粉末を配合・混合し、得られた原料混合粉末を大気中、900〜1250℃の温度範囲で仮焼した後、粉砕、水洗処理し、次いで、大気中、700〜1100℃の温度範囲でアニール加熱処理するボンド磁石用マグネトプランバイト型フェライト粒子粉末材料の製造方法において、前記仮焼以降のいずれかの工程におけるマグネトプランバイト型フェライト粒子粉末に対して、Ca化合物を前記フェライト粒子粉末に対して、1500〜30000mg/kg(0.15〜3.00重量%)添加することを特徴とする請求項1記載のボンド磁石用マグネトプランバイト型フェライト粒子粉末材料の製造方法。 After mixing and mixing the raw material powder, the obtained raw material mixed powder was calcined in the temperature range of 900 to 1250 ° C. in the atmosphere, then pulverized and washed, and then in the temperature range of 700 to 1100 ° C. in the air. In the manufacturing method of the magnetoplumbite type ferrite particle powder material for bonded magnet to be annealed and heated, the Ca compound is added to the ferrite particle powder with respect to the magnetoplumbite type ferrite particle powder in any step after the calcination. The method for producing a magnetoplumbite-type ferrite particle powder material for bonded magnets according to claim 1, wherein 1500 to 30000 mg / kg (0.15 to 3.00% by weight) is added. 請求項1記載のボンド磁石用マグネトプランバイト型フェライト粒子粉末を用いた樹脂組成物。 A resin composition using the magnetoplumbite type ferrite particle powder for bonded magnets according to claim 1. 請求項1記載のボンド磁石用マグネトプランバイト型フェライト粒子粉末を用いたボンド磁石。 A bonded magnet using the magnetoplumbite type ferrite particle powder for bonded magnet according to claim 1. 請求項1記載のボンド磁石用マグネトプランバイト型フェライト粒子粉末を用いたマグネットロール。
A magnet roll using the magnetoplumbite type ferrite particle powder for bonded magnets according to claim 1.
JP2008014219A 2008-01-24 2008-01-24 Magnetoplumbite type ferrite particle powder for bonded magnet and method for producing the same, resin composition using the magnetoplumbite type ferrite particle powder, bonded magnet and magnet roll Expired - Fee Related JP5267771B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP2008014219A JP5267771B2 (en) 2008-01-24 2008-01-24 Magnetoplumbite type ferrite particle powder for bonded magnet and method for producing the same, resin composition using the magnetoplumbite type ferrite particle powder, bonded magnet and magnet roll

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP2008014219A JP5267771B2 (en) 2008-01-24 2008-01-24 Magnetoplumbite type ferrite particle powder for bonded magnet and method for producing the same, resin composition using the magnetoplumbite type ferrite particle powder, bonded magnet and magnet roll

Publications (2)

Publication Number Publication Date
JP2009176960A true JP2009176960A (en) 2009-08-06
JP5267771B2 JP5267771B2 (en) 2013-08-21

Family

ID=41031743

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2008014219A Expired - Fee Related JP5267771B2 (en) 2008-01-24 2008-01-24 Magnetoplumbite type ferrite particle powder for bonded magnet and method for producing the same, resin composition using the magnetoplumbite type ferrite particle powder, bonded magnet and magnet roll

Country Status (1)

Country Link
JP (1) JP5267771B2 (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
KR20150138200A (en) * 2013-04-03 2015-12-09 도다 고교 가부시끼가이샤 Ferrite particle powder for bonded magnet, resin composition for bonded magnet, and molded body using same
US11823823B2 (en) 2013-10-02 2023-11-21 Toda Kogyo Corporation Ferrite particles for bonded magnets, resin composition for bonded magnets, and molded product using the same

Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH0480903A (en) * 1990-07-24 1992-03-13 Kawasaki Steel Corp Manufacture of forming material for bonded magnet
JPH11195517A (en) * 1997-09-19 1999-07-21 Tdk Corp Hexagonal-ferrite magnet powder and manufacture of hexagonal-ferrite sintered magnet
JPH11283819A (en) * 1998-03-31 1999-10-15 Nippon Bengara Kogyo Kk Ferrite magnetic powder for bonded magnet and its manufacture
JP2003048772A (en) * 2001-06-01 2003-02-21 Tdk Corp Method for producing ferritic sintered magnet
JP2006117515A (en) * 2004-09-21 2006-05-11 Tdk Corp Method for producing ferrite magnetic material

Patent Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH0480903A (en) * 1990-07-24 1992-03-13 Kawasaki Steel Corp Manufacture of forming material for bonded magnet
JPH11195517A (en) * 1997-09-19 1999-07-21 Tdk Corp Hexagonal-ferrite magnet powder and manufacture of hexagonal-ferrite sintered magnet
JPH11283819A (en) * 1998-03-31 1999-10-15 Nippon Bengara Kogyo Kk Ferrite magnetic powder for bonded magnet and its manufacture
JP2003048772A (en) * 2001-06-01 2003-02-21 Tdk Corp Method for producing ferritic sintered magnet
JP2006117515A (en) * 2004-09-21 2006-05-11 Tdk Corp Method for producing ferrite magnetic material

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
KR20150138200A (en) * 2013-04-03 2015-12-09 도다 고교 가부시끼가이샤 Ferrite particle powder for bonded magnet, resin composition for bonded magnet, and molded body using same
EP2983178A4 (en) * 2013-04-03 2016-10-26 Toda Kogyo Corp Ferrite particle powder for bonded magnet, resin composition for bonded magnet, and molded body using same
KR102231072B1 (en) * 2013-04-03 2021-03-22 도다 고교 가부시끼가이샤 Ferrite particle powder for bonded magnet, resin composition for bonded magnet, and molded body using same
US11820055B2 (en) 2013-04-03 2023-11-21 Toda Kogyo Corp. Ferrite particles for bonded magnets, resin composition for bonded magnets, and molded product using the same
US11823823B2 (en) 2013-10-02 2023-11-21 Toda Kogyo Corporation Ferrite particles for bonded magnets, resin composition for bonded magnets, and molded product using the same

Also Published As

Publication number Publication date
JP5267771B2 (en) 2013-08-21

Similar Documents

Publication Publication Date Title
JP5393989B2 (en) Ferrite particle powder for bonded magnet, resin composition for bonded magnet, and molded body using them
JP4877513B2 (en) Ferrite particle powder for bonded magnet, resin composition for bonded magnet, and molded body using them
US11823823B2 (en) Ferrite particles for bonded magnets, resin composition for bonded magnets, and molded product using the same
JP6459963B2 (en) Ferrite particle powder for bonded magnet, resin composition for bonded magnet, and molded body using them
CN106795006B (en) Ferrite particle powder for bonded magnet, resin composition for bonded magnet, and molded body using same
JP5360445B2 (en) Ferrite particle powder for bonded magnet, resin composition for bonded magnet, and molded body using them
JP5267771B2 (en) Magnetoplumbite type ferrite particle powder for bonded magnet and method for producing the same, resin composition using the magnetoplumbite type ferrite particle powder, bonded magnet and magnet roll
JP4893680B2 (en) Ferrite particle powder for bonded magnet, resin composition for bonded magnet, and molded body using them

Legal Events

Date Code Title Description
A621 Written request for application examination

Free format text: JAPANESE INTERMEDIATE CODE: A621

Effective date: 20101110

A521 Written amendment

Free format text: JAPANESE INTERMEDIATE CODE: A523

Effective date: 20111020

A977 Report on retrieval

Free format text: JAPANESE INTERMEDIATE CODE: A971007

Effective date: 20120713

A131 Notification of reasons for refusal

Free format text: JAPANESE INTERMEDIATE CODE: A131

Effective date: 20120725

TRDD Decision of grant or rejection written
A01 Written decision to grant a patent or to grant a registration (utility model)

Free format text: JAPANESE INTERMEDIATE CODE: A01

Effective date: 20130410

A61 First payment of annual fees (during grant procedure)

Free format text: JAPANESE INTERMEDIATE CODE: A61

Effective date: 20130423

R150 Certificate of patent or registration of utility model

Free format text: JAPANESE INTERMEDIATE CODE: R150

Ref document number: 5267771

Country of ref document: JP

Free format text: JAPANESE INTERMEDIATE CODE: R150

R250 Receipt of annual fees

Free format text: JAPANESE INTERMEDIATE CODE: R250

R250 Receipt of annual fees

Free format text: JAPANESE INTERMEDIATE CODE: R250

R250 Receipt of annual fees

Free format text: JAPANESE INTERMEDIATE CODE: R250

R250 Receipt of annual fees

Free format text: JAPANESE INTERMEDIATE CODE: R250

R250 Receipt of annual fees

Free format text: JAPANESE INTERMEDIATE CODE: R250

S531 Written request for registration of change of domicile

Free format text: JAPANESE INTERMEDIATE CODE: R313531

R350 Written notification of registration of transfer

Free format text: JAPANESE INTERMEDIATE CODE: R350

LAPS Cancellation because of no payment of annual fees