JP3968964B2 - Steel plate for heat shrink band - Google Patents
Steel plate for heat shrink band Download PDFInfo
- Publication number
- JP3968964B2 JP3968964B2 JP2000198653A JP2000198653A JP3968964B2 JP 3968964 B2 JP3968964 B2 JP 3968964B2 JP 2000198653 A JP2000198653 A JP 2000198653A JP 2000198653 A JP2000198653 A JP 2000198653A JP 3968964 B2 JP3968964 B2 JP 3968964B2
- Authority
- JP
- Japan
- Prior art keywords
- steel
- magnetic
- permeability
- less
- content
- 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 - Fee Related
Links
Images
Classifications
-
- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22C—ALLOYS
- C22C38/00—Ferrous alloys, e.g. steel alloys
- C22C38/02—Ferrous alloys, e.g. steel alloys containing silicon
-
- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22C—ALLOYS
- C22C38/00—Ferrous alloys, e.g. steel alloys
- C22C38/002—Ferrous alloys, e.g. steel alloys containing In, Mg, or other elements not provided for in one single group C22C38/001 - C22C38/60
-
- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22C—ALLOYS
- C22C38/00—Ferrous alloys, e.g. steel alloys
- C22C38/004—Very low carbon steels, i.e. having a carbon content of less than 0,01%
-
- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22C—ALLOYS
- C22C38/00—Ferrous alloys, e.g. steel alloys
- C22C38/04—Ferrous alloys, e.g. steel alloys containing manganese
-
- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22C—ALLOYS
- C22C38/00—Ferrous alloys, e.g. steel alloys
- C22C38/60—Ferrous alloys, e.g. steel alloys containing lead, selenium, tellurium, or antimony, or more than 0.04% by weight of sulfur
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01J—ELECTRIC DISCHARGE TUBES OR DISCHARGE LAMPS
- H01J29/00—Details of cathode-ray tubes or of electron-beam tubes of the types covered by group H01J31/00
- H01J29/86—Vessels; Containers; Vacuum locks
- H01J29/867—Means associated with the outside of the vessel for shielding, e.g. magnetic shields
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01J—ELECTRIC DISCHARGE TUBES OR DISCHARGE LAMPS
- H01J29/00—Details of cathode-ray tubes or of electron-beam tubes of the types covered by group H01J31/00
- H01J29/86—Vessels; Containers; Vacuum locks
- H01J29/87—Arrangements for preventing or limiting effects of implosion of vessels or containers
-
- C—CHEMISTRY; METALLURGY
- C21—METALLURGY OF IRON
- C21D—MODIFYING THE PHYSICAL STRUCTURE OF FERROUS METALS; GENERAL DEVICES FOR HEAT TREATMENT OF FERROUS OR NON-FERROUS METALS OR ALLOYS; MAKING METAL MALLEABLE, e.g. BY DECARBURISATION OR TEMPERING
- C21D8/00—Modifying the physical properties of ferrous metals or ferrous alloys by deformation combined with, or followed by, heat treatment
- C21D8/02—Modifying the physical properties of ferrous metals or ferrous alloys by deformation combined with, or followed by, heat treatment during manufacturing of plates or strips
- C21D8/0221—Modifying the physical properties of ferrous metals or ferrous alloys by deformation combined with, or followed by, heat treatment during manufacturing of plates or strips characterised by the working steps
- C21D8/0226—Hot rolling
-
- C—CHEMISTRY; METALLURGY
- C21—METALLURGY OF IRON
- C21D—MODIFYING THE PHYSICAL STRUCTURE OF FERROUS METALS; GENERAL DEVICES FOR HEAT TREATMENT OF FERROUS OR NON-FERROUS METALS OR ALLOYS; MAKING METAL MALLEABLE, e.g. BY DECARBURISATION OR TEMPERING
- C21D8/00—Modifying the physical properties of ferrous metals or ferrous alloys by deformation combined with, or followed by, heat treatment
- C21D8/02—Modifying the physical properties of ferrous metals or ferrous alloys by deformation combined with, or followed by, heat treatment during manufacturing of plates or strips
- C21D8/0221—Modifying the physical properties of ferrous metals or ferrous alloys by deformation combined with, or followed by, heat treatment during manufacturing of plates or strips characterised by the working steps
- C21D8/0236—Cold rolling
Landscapes
- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Mechanical Engineering (AREA)
- Metallurgy (AREA)
- Organic Chemistry (AREA)
- Heat Treatment Of Sheet Steel (AREA)
- Soft Magnetic Materials (AREA)
- Manufacturing Of Steel Electrode Plates (AREA)
Description
【0001】
【発明の属する技術分野】
本発明は、カラー陰極線管のパネル周囲を緊締するヒートシュリンクバンド用鋼板に関するものである。
【0002】
【従来の技術】
カラー陰極線管(以下、CRTと称す)では、管体内が1.0×10-7Torr程度の高真空状態であることから、パネル面の変形防止および管体の内爆防止といった処理を必要としている。このような処理としては、バンド状に成形した鋼板からなるヒートシュリンクバンド(以下、HSバンドと称す)を400℃から600℃程度の温度で数秒〜数十秒間加熱・膨張させ、CRTガラスパネルにはめ込み、冷却・収縮によって張力を付与する、いわゆる焼ばめ処理によってパネル面の変形を補正する方法が挙げられる。
【0003】
従来、上記焼ばめ処理に使用されるHSバンド材は軽量でかつ所定の強度と延性を具備することが課題とされ、HSバンド材としてはメッキを施した板厚0.8〜2mmの冷延鋼板が使用されていた。ところがその後、HSバンド材に地磁気等の外部磁界の遮蔽効果を付与することで、電子ビームの着弾地のずれにより生じる色ずれを大幅に低減できることが見いだされ、磁気シールド性が新たな鋼板性能として着目されている。
【0004】
上記のようにHSバンド材に高い強度を持たせながら高い磁気シールド性も付与する方法として、例えば特開平11−86755号公報には、Siを1〜2%含有させてSiの固溶強化を活用するとともに、地磁気レベルの透磁率を向上させる方法が、また、特開平11−158549号公報にはSi含有鋼の介在物組成を適正化して保磁力を向上させるとともに、結晶粒径を適正化して高強度化を図る方法がそれぞれ開示されている。
【0005】
【発明が解決しようとする課題】
最近ではTV受像管のさらなる軽量化が指向され、HSバンド材の薄肉化に対する要望が益々強くなりつつある。一方、テレビの大画面化や平面化、コンピュータモニタの高精細化に伴い、磁気シールド性(すなわち高透磁率化等の磁気特性)への要求も厳しくなり、HSバンド材では磁気特性向上も切望されている。このように、HSバンド材にはさらなる高強度化および磁気特性向上(高透磁率化)が強く求められているのが現状である。
【0006】
しかしながら、上記従来技術では、強度と透磁率を向上させる方法として、Si、Mn、P等の元素を多量に含有させる方法、および結晶粒径を適正化する方法をとっているが、特開平11−86755号公報記載の方法では溶接性や製造コストの面からさらにSi、Mn、P等の含有量を増加させることは難しく、これ以上の高強度、高透磁率化は難しいといえる。また、特開平11−158549号公報記載の方法では、細粒化により高強度化は図られるものの、同時に透磁率の低下を招くので、所望の強度レベルを達成しようとすれば透磁率が不十分となる。
【0007】
以上のように、従来技術では最近のニーズに応えるべく優れた強度と磁気特性を兼ね備えた鋼板は得られていない。
【0008】
本発明はこのような事情に鑑みなされたものであり、強度と透磁率とのバランスに優れた鋼板を提供することを目的とする。
【0009】
【課題を解決するための手段】
本発明者らは、粗大な析出物を形成しやすいBに着目して、HSバンド材の高強度、高透磁率化を図るべく鋭意研究を重ねた。その結果、以下の知見を得た。
【0010】
▲1▼磁気特性の向上に有効な元素であるBは、Oとの親和力が強いので、鋳造時に微細介在物であるB2O5を生成しやすい。
【0011】
▲2▼スラブ加熱時には表層でBの酸化が進行してBの枯渇層が生じやすい。
【0012】
▲3▼さらに、BはNとの親和力も強いのでスラブ加熱時や焼鈍時に表層窒化が生じやすく、Nと結合して粗大な析出物を形成しやすい。
【0013】
▲4▼上記のようなB2O5、Bの枯渇層及び表層窒化が生じると、B添加の効果が十分活かされない。
【0014】
▲5▼B2O5、Bの枯渇層及び表層窒化の生成を防ぎ、B添加の効果を十分活かすためには、鋳造時のO含有量を一定量以下にまで十分低減し、なおかつSbをBと複合して適量添加することが有効である。
【0015】
本発明はかかる知見に基づきなされたもので、以下の構成を有する。
[1]mass%で、C:0.005%以下、Si:0.5〜4%、Mn:2%以下、sol.Al:0.2 %以下、S:0.04%以下、P:0.2%以下、N:0.01%以下、B:0.0003〜0.004%、T.O.:0.005%以下、Sb:0.002〜0.1%を含有し、残部Fe および不可避不純物からなるヒートシュリンクバンド用鋼板。
【0016】
[2] 上記[1]において、B量とN量がB/N:0.2〜1を満足することを特徴とするヒートシュリンクバンド用鋼板。
【0017】
なお、本明細書において、鋼の成分を示す%はすべてmass%である。
【0018】
【発明の実施の形態】
以下、本発明の詳細をその限定理由とともに説明する。
まず、種々のB含有鋼について抽出残渣の化学分析、透過電子顕微鏡観察等を行い、析出物、介在物の詳細調査を行った。その結果、B含有鋼では、窒化物以外に酸化物であるB2O5が生じており、この酸化物生成量が比較的多い鋼において透磁率が劣る傾向が認められた。そして、電子顕微鏡観察の結果、この酸化物の大きさは比較的微細であることが判明し、この酸化物自体が透磁率に悪影響を及ぼしていると推定された。Bは酸素との親和力が強いので、溶鋼の鋳造時に十分溶存酸素が低減されていないと、酸化物であるB2O5が形成されるものと考えられる。
【0019】
そこで、B含有鋼の磁気特性向上を目的に、磁気特性に及ぼす酸素含有量を調査した。
【0020】
C:0.002%、Si:1.2%、Mn:1%、P:0.07%、S:0.004%、sol.Al:tr.または0.01%、N:0.002%、B:0.0016%、とし、T.O.を0.001〜0.01%と変化させた鋼を溶製した。ここで、T.O.量(酸素含有量)は、SiまたはAlを添加してからの脱ガス処理時間を調節することにより調整し、Bは、溶存酸素量が高い段階で添加すると鋳造前の段階で酸化物として消費される可能性があるので、それを防止するために、Si、Alを添加し、その後、溶鋼を鋳造する直前に添加した。次いで、熱間圧延および板厚1.2mmまで冷間圧延を施し、680〜730℃で焼鈍を行うことにより結晶粒径を調整し、強度レベル:YP=330〜340MPaの供試材を得た。
【0021】
得られた供試材から25cmエプスタインサンプルを採取して磁気特性を測定した。なお、磁気特性(透磁率)は、23.9A/m(0.3エールステッド)まで磁化したときの比透磁率で評価した。また、酸素含有量は、熱延板と最終焼鈍板にほとんど差が認められないことを事前に確認して、ここでは板厚1.2mmの最終焼鈍板から採取したサンプルについて調査した結果を用いた。
【0022】
図1に、このようにして得られた供試材の酸素含有量(T.O.)と比透磁率の関係を示す。なお、図1において、sol.Al:tr.の鋼の磁気特性を○で、sol.Al:0.01%の鋼の磁気特性を●で示す。
【0023】
図1より、B含有鋼の比透磁率は鋼の酸素含有量と密接に関係しており、sol.Al:tr.の供試材(図中○)、 sol.Al:0.01%の供試材(図中●)ともに、T.O.を0.005%以下に低減すると高い比透磁率が得られることが判明した。 また、T.O.が0.005%以下の鋼板について析出物、介在物の調査を実施したところ、Bはほぼ完全に窒化物として存在しており、酸化物はsol.Al:tr.鋼ではSiO2、sol.Al:0.01%鋼ではAl2O3が主体となっていることが確認された。
【0024】
以上の結果より、酸素含有量(T.O.)は0.005%以下とする。
次に、B含有鋼におけるSb添加の効果について調査した。
本発明鋼では透磁率を向上させる目的で、Cの含有量を0.005%以下としている。このような、いわゆる極低炭素鋼では、スラブの加熱時あるいは焼鈍時に表層でのC以外の元素の酸化が生じやすくなる。この原因は必ずしも明らかではないが、Cが十分存在する場合にはCが優先酸化されるが、Cの含有量が少ないとその効果が十分得られず、他の元素の酸化が生じてしまうものと考えられる。本発明鋼では、B含有鋼を用いているため、表層でのBの酸化反応が進行しやすいと考えられる。
【0025】
また、BはNとの親和力も強いので、スラブ加熱時、焼鈍時等において、表層で炉内雰囲気成分として存在する窒素と結合しやすく、鋼板表層では窒化が生じやすいと考えられる。
【0026】
そこで、表層でのBの酸化、窒化防止を目的に、B含有鋼へのSbの複合添加を検討した。C:0.002%、Si:1.2%、Mn:1%、P:0.07%、S:0.004%、sol.Al:0.02%、N:0.002%、B:tr.または0.0015%、T.O.:0.002%とし、Sbをtr.〜0.2%と変化させた鋼を溶製し、図1と同様の条件で熱延、冷延、焼鈍を施し供試材を得た。
【0027】
次いで、得られた供試材から25cmエプスタインサンプルを採取して磁気特性を測定した。なお、磁気特性(透磁率)の測定及び酸素含有量の測定は、図1と同様の方法にて行った。
【0028】
図2にこのようにして得られた供試材のSb添加量と比透磁率の関係を示す。なお、図2において、B:tr.の鋼の比透磁率を●で、B:0.0015%の鋼(B含有鋼)の比透磁率を○で示した。
【0029】
図2により、B含有鋼(図中○)ではSbを0.002〜0.1%の範囲で含有させることにより、さらに比透磁率が向上することがわかる。
【0030】
B含有鋼のSb:tr.材と、Sb:0.02%材について表層からの深さ方向にB、Nの化学分析を行ったところ、Sb:tr.材では表層からの深さ50μm付近までの領域でBの含有量が減少していることが判明した。これは、Bが鋼の表層で優先酸化され、Bの含有量が減少したものと推測される。また、表層からの深さ30μm付近までの領域ではNの含有量が鋼板内部と比べてわずかに増加しており、窒化も生じていることが判明した。
【0031】
一方、Sb:0.02%材では酸化、窒化ともに軽減されていた。Sb:0.02%材では鋼の表層での酸化、窒化が防止されて磁気特性が向上したものと考えられる。
【0032】
以上の理由により、Sbの添加量は0.002〜0.1%とする。
次に、さらに磁気特性を向上させるために、B含有量と磁気特性の関係を調査した。C:0.002%、Si:1.2%、Mn:1%、P:0.07%、S:0.004%、sol.Al:0.01%、N:0.003%としBをtr.〜0.006%と変化させ、さらにT.O.およびSbの含有量を、T.O.:0.006%、Sb:tr.に調整した鋼、T.O.:0.002%、Sb:tr.に調整した鋼、T.O.:0.002%、Sb:0.01%に調整した鋼に図1と同様の条件で溶製、熱延、冷延、焼鈍を施し供試材を得た。
【0033】
次いで、得られた供試材から25cmエプスタインサンプルを採取して磁気特性を測定した。なお、磁気特性(透磁率)の測定及び酸素含有量の測定は、図1と同様の方法にて行った。
【0034】
図3にこのようにして得られた供試材のB含有量、B/Nと比透磁率の関係を示す。なお、図3において、T.O.:0.006%、Sb:tr.に調整した鋼の比透磁率を▲で、T.O.:0.002%、Sb:tr.を含有する鋼の比透磁率を●で、T.O.:0.002%、Sb:0.01%を含有する鋼の比透磁率を○で示した。
【0035】
図3より、T.O:0.006%、Sb:tr.に調整した鋼(図中▲)では、比透磁率の値にやや多くのばらつきを有しており、B/N=1.2付近で極大をとる。また、T.O:0.002%、Sb:tr.に調整した鋼(図中●)では、比透磁率のばらつきがT.O.:0.006%を含有する鋼より改善されるとともに、その値も向上し、比透磁率はB/N=0.9付近で極大となる。
【0036】
一方、T.O.:0.002%、Sb:0.01%に調整した鋼(図中○)では、BとSbの複合添加の効果により、 T.O:0.002%、Sb:tr.鋼よりさらに比透磁率が向上し、B/N=0.7付近で極大となる。以上のように、酸素含有量を適正化した鋼にBとSbを複合して添加することにより、比透磁率が大幅に向上し、さらにB/Nを適正範囲にすることによりさらに比透磁率が向上することがわかる。
【0037】
以上の理由により、Bの含有量は、磁気特性の向上効果が認められる0.0003〜0.004%の範囲とする。また、より磁気特性を向上させるためには、BとNをB/Nで0.2〜1の範囲とすることが好ましい。
【0038】
次に、他の成分の限定理由について説明する。
C:0.005%を超えて含有するとカーバイドが析出し、透磁率を劣化させる。したがって、Cは0.005%以下とする。
【0039】
Si:強度を増加させると同時に透磁率を向上させる重要な元素である。Si添加による強度上昇および透磁率向上の効果を発揮させるには、0.5%以上の添加が必要である。一方、Siを4%超えで添加しても透磁率の改善効果は小さくいたずらにコスト上昇を招く。さらには、溶接性の劣化、脆化等も招く。したがって、Siの含有量は、0.5〜4%とする。
【0040】
Mn:透磁率の劣化が比較的小さく、なおかつ固溶体強化により強度を上昇させる元素である。したがって、Mnは強度を確保するために適量添加することが望ましい。ただし、2%を超えて添加すると磁気特性が劣化する。以上より、Mnは2%以下とする。
【0041】
P:透磁率の劣化が小さく、なおかつ微量でも固溶体強化能が大きい元素である。したがって、積極的に活用することが望ましい元素である。ただし、0.2%超えで添加すると溶接性が著しく劣化するので0.2%以下とする。
【0042】
sol.Al:添加は必須では無いが、T.O.を低減する目的で含有させることが望ましい。しかし、0.2%を超えて含有させると、B含有の効果が得られず、いたずらにコストアップを招くので、0.2%以下とする。また、酸化物を安定してSiO2とするためには0.001%以下、もしくはAl2O3とするためには0.005%以上含有させることが望ましい。
【0043】
N:析出物を形成しやすく、磁気特性を劣化させる元素である。したがって、0.01%以下とする。
【0044】
また、本発明においては、Sbと比べてその効果は非常に小さいものの、酸化、窒化を防止する目的で、例えば、Sn:0.003〜0.15%、Cu:0.05〜0.2%等を1種または2種以上で複合して添加してもよい。
【0045】
次に本発明のヒートシュリンクバンド用鋼板の製造方法について説明する。
本発明においては、本発明で規定する成分が本発明の範囲内であればよく、本発明の鋼板を得るには、例えば、転炉で吹練した溶鋼を脱ガス処理し所定の成分に調整し、引き続き鋳造、熱間圧延を行う。熱間圧延時の仕上焼鈍温度、巻取り温度は特に規定する必要はなく、通常でかまわない。また、熱間圧延後の熱延板焼鈍は行っても良いが必須ではない。次いで一回の冷間圧延、もしくは中間焼鈍をはさんだ2回以上の冷間圧延により所定の板厚とした後に、最終(仕上)焼鈍を行う。
【0046】
なお、HSバンド材として、耐食性の観点からメッキを施してもよい。メッキ種は特に限定されるものではなく、例えば、Zn、Zn−Ni合金、Zn−Al合金、Ni、Al、Sn、Crなどの単層メッキ、またはこれらの復層メッキ、あるいはメッキと地鉄とを一部または全部合金化させたメッキなどが適用可能である。
また、鋼板表面あるいはメッキ表面に各種の化成処理皮膜を形成してもよい。
【0047】
【実施例】
転炉で吹練した溶鋼を脱ガス処理し、所定の成分に鋳造後、1150℃×1hrのスラブ加熱を行った後、板厚3.2mmまで熱間圧延を行った。ここで、巻き取り温度は680℃とした。その後、酸洗を行い、引き続き、板厚1.2mmまで冷間圧延を行い、10%H2−90%N2雰囲気で680℃〜820℃×60secの仕上焼鈍を行った。また、一部の鋼板については、焼鈍後に伸長率:0.5〜1.5%のスキンパス圧延を行った。
仕上焼鈍後の鋼板の化学成分を表1に示す。
【0048】
【表1】
【0049】
得られた各鋼板の機械特性及び磁気特性を表2に示す。
ここで、機械特性(YPEL)の測定はJIS5号引張試験片にて行い、磁気測定は25cmエプスタイン試験片を用いて行った。なお、磁気特性は23.9A/mまで磁化したときの透磁率で評価した。
【0050】
【表2】
【0051】
表2より、鋼板成分を本発明範囲に制御した本発明例では、良好な磁気特性および高い強度を有する鋼板が得られていることがわかる。一方、比較例では、強度が劣っているかもしくは透磁率が低いことがわかる。
【0052】
【発明の効果】
以上述べたように、本発明によれば、磁気特性と強度とのバランスに優れたHSバンド用鋼板を得ることができる。
【0053】
また、本発明は、結晶粒の粗大化等の手段を用いない為、透磁率を向上させてもほとんど強度低下を伴わないので、強度レベルを維持しつつ透磁率の向上を図ることができる。
【図面の簡単な説明】
【図1】酸素含有量と比透磁率の関係を示すグラフ。
【図2】Sb含有量と比透磁率の関係を示すグラフ。
【図3】B含有量、B/Nと比透磁率の関係を示すグラフ。[0001]
BACKGROUND OF THE INVENTION
The present invention relates to a steel plate for a heat shrink band that tightens around the panel of a color cathode ray tube.
[0002]
[Prior art]
In a color cathode ray tube (hereinafter referred to as CRT), since the inside of the tube is in a high vacuum state of about 1.0 × 10 −7 Torr, processing such as prevention of deformation of the panel surface and prevention of internal explosion of the tube is required. Yes. As such a treatment, a heat shrink band (hereinafter referred to as an HS band) made of a steel plate formed into a band shape is heated and expanded at a temperature of about 400 ° C. to 600 ° C. for several seconds to several tens of seconds to form a CRT glass panel. A method of correcting the deformation of the panel surface by a so-called shrink fitting process in which tension is applied by fitting, cooling / shrinking may be mentioned.
[0003]
Conventionally, HS band materials used for the above-mentioned shrink-fitting treatment have been required to be lightweight and have a predetermined strength and ductility. As HS band materials, cold plated plates with a thickness of 0.8 to 2 mm are used. A rolled steel sheet was used. However, after that, it was found that by giving the HS band material the shielding effect of the external magnetic field such as geomagnetism, the color shift caused by the shift of the landing spot of the electron beam can be greatly reduced, and the magnetic shielding property is a new steel plate performance. It is attracting attention.
[0004]
As a method for imparting high magnetic shielding properties while giving high strength to the HS band material as described above, for example, in Japanese Patent Application Laid-Open No. 11-86755, Si is included in a solid solution strengthening by containing 1 to 2%. A method for improving the magnetic permeability at the geomagnetic level is disclosed in JP-A-11-158549. The inclusion composition of Si-containing steel is optimized to improve the coercive force, and the crystal grain size is optimized. A method for increasing the strength is disclosed.
[0005]
[Problems to be solved by the invention]
Recently, further weight reduction of TV picture tubes has been aimed at, and the demand for thinner HS band materials is becoming stronger. On the other hand, the demand for magnetic shielding (that is, magnetic properties such as high permeability) has become stricter with the increase in screen size and flatness of televisions and the increase in definition of computer monitors. Has been. As described above, the HS band material is strongly demanded to further increase the strength and improve the magnetic characteristics (high permeability).
[0006]
However, in the above prior art, as a method for improving the strength and the magnetic permeability, a method of containing a large amount of elements such as Si, Mn, and P and a method of optimizing the crystal grain size are employed. In the method described in Japanese Patent No. -86755, it is difficult to further increase the content of Si, Mn, P and the like from the viewpoint of weldability and manufacturing cost, and it can be said that higher strength and higher permeability are difficult. Further, in the method described in JP-A No. 11-158549, although the strength can be increased by making fine particles, the magnetic permeability is lowered at the same time, so that the magnetic permeability is insufficient if an attempt is made to achieve a desired strength level. It becomes.
[0007]
As described above, in the prior art, a steel sheet having excellent strength and magnetic properties to meet recent needs has not been obtained.
[0008]
This invention is made | formed in view of such a situation, and it aims at providing the steel plate excellent in the balance of an intensity | strength and magnetic permeability.
[0009]
[Means for Solving the Problems]
The inventors of the present invention have made extensive studies in order to increase the strength and permeability of the HS band material while paying attention to B that easily forms coarse precipitates. As a result, the following knowledge was obtained.
[0010]
{Circle around (1)} B, which is an element effective in improving the magnetic properties, has a strong affinity for O, so it is easy to produce B 2 O 5 that is a fine inclusion during casting.
[0011]
(2) When the slab is heated, oxidation of B proceeds on the surface layer, and a B depleted layer is likely to occur.
[0012]
(3) Further, since B has a strong affinity for N, surface layer nitriding is likely to occur during slab heating or annealing, and it is easy to bond with N to form coarse precipitates.
[0013]
{Circle around (4)} When the B 2 O 5 and B depletion layers and surface nitridation as described above occur, the effect of B addition is not fully utilized.
[0014]
(5) In order to prevent the formation of B 2 O 5 and B depletion layers and surface nitriding and to fully utilize the effect of B addition, the O content during casting is sufficiently reduced to a certain amount or less, and Sb is reduced. It is effective to add an appropriate amount in combination with B.
[0015]
This invention is made | formed based on this knowledge, and has the following structures.
[1] In mass%, C: 0.005% or less, Si: 0.5 to 4%, Mn: 2% or less, sol. Al: 0.2% or less, S: 0.04% or less, P: 0.2% or less, N: 0.01% or less, B: 0.0003 to 0.004%, T.P. O. : 0.005% or less, Sb: 0.002 to 0.1%, a steel sheet for heat shrink band made of the remaining Fe and inevitable impurities .
[0016]
[2] A steel sheet for heat shrink band according to [1], wherein the B content and the N content satisfy B / N: 0.2 to 1.
[0017]
In addition, in this specification, all% which shows the component of steel is mass%.
[0018]
DETAILED DESCRIPTION OF THE INVENTION
Hereinafter, the details of the present invention will be described together with the reasons for limitation.
First, various B-containing steels were subjected to chemical analysis of the extraction residue, observation with a transmission electron microscope, and the like, and a detailed investigation of precipitates and inclusions was performed. As a result, in the B-containing steel, B 2 O 5 , which is an oxide, was generated in addition to the nitride, and a tendency for the permeability to be inferior in steel having a relatively large amount of oxide generation was recognized. As a result of observation with an electron microscope, the size of the oxide was found to be relatively fine, and it was estimated that the oxide itself had an adverse effect on the magnetic permeability. Since B has a strong affinity for oxygen, it is considered that B 2 O 5, which is an oxide, is formed if the dissolved oxygen is not sufficiently reduced during casting of molten steel.
[0019]
Then, the oxygen content which influences a magnetic characteristic was investigated for the purpose of the magnetic characteristic improvement of B containing steel.
[0020]
C: 0.002%, Si: 1.2%, Mn: 1%, P: 0.07%, S: 0.004%, sol. Al: tr. Or 0.01%, N: 0.002%, B: 0.0016%. O. The steel was changed from 0.001 to 0.01%. Here, T.W. O. The amount (oxygen content) is adjusted by adjusting the degassing time after adding Si or Al, and B is consumed as an oxide at the stage before casting when added at a stage where the dissolved oxygen amount is high. In order to prevent this, Si and Al were added, and then added immediately before casting the molten steel. Subsequently, hot rolling and cold rolling to a sheet thickness of 1.2 mm were performed, and the crystal grain size was adjusted by annealing at 680 to 730 ° C. to obtain a test material having a strength level of YP = 330 to 340 MPa. .
[0021]
A 25 cm Epstein sample was taken from the obtained test material, and the magnetic properties were measured. The magnetic properties (permeability) were evaluated by the relative permeability when magnetized to 23.9 A / m (0.3 alested). In addition, the oxygen content was confirmed in advance that there was almost no difference between the hot-rolled sheet and the final annealed sheet. Here, the results obtained by examining a sample collected from the final annealed sheet having a thickness of 1.2 mm were used. It was.
[0022]
FIG. 1 shows the relationship between the oxygen content (TO) and the relative permeability of the test material thus obtained. In FIG. 1, sol. Al: tr. The magnetic properties of the steels of No. Al: Magnetic properties of 0.01% steel are indicated by ●.
[0023]
From FIG. 1, the relative permeability of B-containing steel is closely related to the oxygen content of the steel. Al: tr. Test material (circle in the figure), sol. Al: 0.01% of the test material (● in the figure) O. It has been found that a high relative magnetic permeability can be obtained when the content is reduced to 0.005% or less. T. O. When the precipitates and inclusions were investigated for a steel sheet with 0.005% or less, B was almost completely present as a nitride, and the oxide was sol. Al: tr. For steel, SiO 2 , sol. It was confirmed that Al: 0.01% steel is mainly composed of Al 2 O 3 .
[0024]
From the above results, the oxygen content (TO) is made 0.005% or less.
Next, the effect of Sb addition in B-containing steel was investigated.
In the steel of the present invention, the C content is set to 0.005% or less for the purpose of improving the magnetic permeability. In such a so-called ultra-low carbon steel, oxidation of elements other than C in the surface layer is likely to occur during heating or annealing of the slab. The cause of this is not necessarily clear, but when C is sufficiently present, C is preferentially oxidized, but if the C content is low, the effect cannot be obtained sufficiently, and oxidation of other elements occurs. it is conceivable that. Since the steel according to the present invention uses B-containing steel, it is considered that the oxidation reaction of B on the surface layer is likely to proceed.
[0025]
In addition, since B has a strong affinity for N, it is considered that it easily binds to nitrogen existing as a furnace atmosphere component in the surface layer during slab heating or annealing, and nitriding is likely to occur in the steel sheet surface layer.
[0026]
Therefore, for the purpose of preventing oxidation and nitridation of B at the surface layer, the combined addition of Sb to the B-containing steel was examined. C: 0.002%, Si: 1.2%, Mn: 1%, P: 0.07%, S: 0.004%, sol. Al: 0.02%, N: 0.002%, B: tr. Or 0.0015%, T.I. O. : 0.002%, Sb is tr. The steel changed to ˜0.2% was melted and subjected to hot rolling, cold rolling and annealing under the same conditions as in FIG.
[0027]
Next, a 25 cm Epstein sample was collected from the obtained test material, and the magnetic properties were measured. In addition, the measurement of a magnetic characteristic (magnetic permeability) and the measurement of oxygen content were performed by the method similar to FIG.
[0028]
FIG. 2 shows the relationship between the Sb addition amount and the relative magnetic permeability of the test material thus obtained. In FIG. 2, B: tr. The relative magnetic permeability of steel No. is indicated by ●, and the relative permeability of B: 0.0015% steel (B-containing steel) is indicated by ○.
[0029]
From FIG. 2, it can be seen that the B-containing steel (◯ in the figure) further improves the relative permeability by containing Sb in a range of 0.002 to 0.1%.
[0030]
B-containing steel Sb: tr. When B and N were subjected to chemical analysis in the depth direction from the surface layer of the Sb: 0.02% material and Sb: tr. In the material, it was found that the B content decreased in the region from the surface layer to a depth of about 50 μm. This is presumed that B was preferentially oxidized in the steel surface layer and the B content was reduced. Further, it was found that in the region from the surface layer to a depth of about 30 μm, the N content slightly increased compared to the inside of the steel sheet, and nitriding occurred.
[0031]
On the other hand, in the Sb: 0.02% material, both oxidation and nitridation were reduced. The Sb: 0.02% material is considered to have improved magnetic properties by preventing oxidation and nitriding on the steel surface layer.
[0032]
For the above reasons, the amount of Sb added is set to 0.002 to 0.1%.
Next, in order to further improve the magnetic characteristics, the relationship between the B content and the magnetic characteristics was investigated. C: 0.002%, Si: 1.2%, Mn: 1%, P: 0.07%, S: 0.004%, sol. Al: 0.01%, N: 0.003%, and B is tr. -0.006%, and T.I. O. And the content of Sb, T. O. : 0.006%, Sb: tr. Steel adjusted to T. O. : 0.002%, Sb: tr. Steel adjusted to T. O. : Steel adjusted to 0.002% and Sb: 0.01% were melted, hot-rolled, cold-rolled and annealed under the same conditions as in Fig. 1 to obtain test materials.
[0033]
Next, a 25 cm Epstein sample was collected from the obtained test material, and the magnetic properties were measured. In addition, the measurement of a magnetic characteristic (magnetic permeability) and the measurement of oxygen content were performed by the method similar to FIG.
[0034]
FIG. 3 shows the relationship between the B content, B / N, and relative permeability of the test material thus obtained. In FIG. O. : 0.006%, Sb: tr. The relative permeability of the steel adjusted to ▲ is T. O. : 0.002%, Sb: tr. The relative permeability of the steel containing でO. : The relative magnetic permeability of steel containing 0.002% and Sb: 0.01% is indicated by ◯.
[0035]
From FIG. O: 0.006%, Sb: tr. The steel adjusted to (▲ in the figure) has a somewhat large variation in the value of relative permeability, and has a maximum near B / N = 1.2. T. O: 0.002%, Sb: tr. In the steel adjusted to (● in the figure), the variation in relative permeability is T.V. O. : It is improved from the steel containing 0.006%, the value is also improved, and the relative magnetic permeability becomes a maximum in the vicinity of B / N = 0.9.
[0036]
On the other hand, T.W. O. : Steel adjusted to 0.002% and Sb: 0.01% (◯ in the figure), due to the combined addition of B and Sb, O: 0.002%, Sb: tr. The relative permeability is further improved than that of steel, and becomes maximum near B / N = 0.7. As described above, by adding B and Sb in combination with steel with an optimized oxygen content, the relative permeability is greatly improved, and further by setting B / N within an appropriate range, the relative permeability is further increased. Can be seen to improve.
[0037]
For the above reasons, the B content is set to a range of 0.0003 to 0.004% where an effect of improving magnetic properties is recognized. In order to further improve the magnetic characteristics, it is preferable that B and N are in the range of 0.2 to 1 in terms of B / N.
[0038]
Next, the reason for limiting other components will be described.
C: When the content exceeds 0.005%, carbide precipitates and the magnetic permeability is deteriorated. Therefore, C is 0.005% or less.
[0039]
Si: An important element that increases the strength and simultaneously improves the magnetic permeability. In order to exhibit the effect of increasing the strength and improving the magnetic permeability by adding Si, it is necessary to add 0.5% or more. On the other hand, even if Si is added in excess of 4%, the effect of improving the magnetic permeability is small, and the cost is increased. Furthermore, deterioration of weldability, embrittlement and the like are also caused. Therefore, the Si content is 0.5-4%.
[0040]
Mn: An element that has a relatively low magnetic permeability deterioration and increases the strength by solid solution strengthening. Therefore, it is desirable to add an appropriate amount of Mn in order to ensure strength. However, if added over 2%, the magnetic properties deteriorate. Accordingly, Mn is set to 2% or less.
[0041]
P: An element having a small magnetic permeability deterioration and a large solid solution strengthening ability even in a small amount. Therefore, it is an element that should be actively utilized. However, if added over 0.2%, the weldability is significantly deteriorated, so the content is made 0.2% or less.
[0042]
sol. Al: Although addition is not essential, T.I. O. It is desirable to make it contain for the purpose of reducing. However, if the content exceeds 0.2%, the effect of containing B cannot be obtained, and the cost is unnecessarily increased, so the content is made 0.2% or less. Further, it is desirable to contain 0.001% or less in order to stably make the oxide SiO 2 or 0.005% or more in order to make Al 2 O 3 .
[0043]
N: An element that easily forms precipitates and deteriorates magnetic properties. Therefore, it is 0.01% or less.
[0044]
In the present invention, the effect is very small compared with Sb, but for the purpose of preventing oxidation and nitridation, for example, Sn: 0.003 to 0.15%, Cu: 0.05 to 0.2 % Or a combination of two or more of them may be added.
[0045]
Next, the manufacturing method of the steel plate for heat shrink bands of this invention is demonstrated.
In the present invention, the components specified in the present invention need only be within the scope of the present invention. To obtain the steel sheet of the present invention, for example, the molten steel blown in a converter is degassed and adjusted to a predetermined component. Subsequently, casting and hot rolling are performed. The finish annealing temperature and the coiling temperature during hot rolling need not be specified and may be normal. Moreover, although hot-rolled sheet annealing after hot rolling may be performed, it is not essential. Next, after a predetermined sheet thickness is obtained by one or more cold rollings or two or more cold rollings with intermediate annealing, final (finishing) annealing is performed.
[0046]
The HS band material may be plated from the viewpoint of corrosion resistance. The type of plating is not particularly limited. For example, Zn, Zn—Ni alloy, Zn—Al alloy, single layer plating such as Ni, Al, Sn, Cr, etc., or their reverse layer plating, or plating and ground iron It is possible to apply plating in which these are partially or wholly alloyed.
Moreover, you may form various chemical conversion treatment films on the steel plate surface or the plating surface.
[0047]
【Example】
The molten steel blown in the converter was degassed, cast into predetermined components, slab heated at 1150 ° C. × 1 hr, and then hot-rolled to a thickness of 3.2 mm. Here, the winding temperature was 680 ° C. Then, pickling was performed, followed by cold rolling to a plate thickness of 1.2 mm, followed by finish annealing at 680 ° C. to 820 ° C. × 60 sec in a 10% H 2 -90% N 2 atmosphere. In addition, some steel plates were subjected to skin pass rolling with an elongation of 0.5 to 1.5% after annealing.
Table 1 shows the chemical composition of the steel sheet after finish annealing.
[0048]
[Table 1]
[0049]
Table 2 shows the mechanical properties and magnetic properties of the obtained steel sheets.
Here, the measurement of mechanical properties (YPEL) was performed using a JIS No. 5 tensile test piece, and the magnetic measurement was performed using a 25 cm Epstein test piece. The magnetic characteristics were evaluated by the magnetic permeability when magnetized to 23.9 A / m.
[0050]
[Table 2]
[0051]
From Table 2, it can be seen that in the present invention example in which the steel plate components are controlled within the range of the present invention, a steel plate having good magnetic properties and high strength is obtained. On the other hand, in a comparative example, it turns out that intensity | strength is inferior or magnetic permeability is low.
[0052]
【The invention's effect】
As described above, according to the present invention, it is possible to obtain a steel sheet for HS band excellent in balance between magnetic properties and strength.
[0053]
In addition, since the present invention does not use means such as coarsening of crystal grains, even if the magnetic permeability is improved, there is almost no decrease in strength, so that the magnetic permeability can be improved while maintaining the strength level.
[Brief description of the drawings]
FIG. 1 is a graph showing the relationship between oxygen content and relative permeability.
FIG. 2 is a graph showing the relationship between Sb content and relative permeability.
FIG. 3 is a graph showing the relationship between B content, B / N, and relative permeability.
Claims (2)
Priority Applications (6)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2000198653A JP3968964B2 (en) | 2000-06-30 | 2000-06-30 | Steel plate for heat shrink band |
| PCT/JP2001/005002 WO2002002838A1 (en) | 2000-06-30 | 2001-06-13 | Steel sheet for heat shrink band |
| CNB018014569A CN1196805C (en) | 2000-06-30 | 2001-06-13 | Steel sheet for heat shrink band |
| EP01941027A EP1310576A4 (en) | 2000-06-30 | 2001-06-13 | Steel sheet for heat shrink band |
| KR10-2002-7001360A KR100468298B1 (en) | 2000-06-30 | 2001-06-13 | Steel Sheet for heat shrink band |
| US10/056,153 US20020139450A1 (en) | 2000-06-30 | 2002-01-24 | Steel sheet for heat shrink band |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2000198653A JP3968964B2 (en) | 2000-06-30 | 2000-06-30 | Steel plate for heat shrink band |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JP2002012942A JP2002012942A (en) | 2002-01-15 |
| JP3968964B2 true JP3968964B2 (en) | 2007-08-29 |
Family
ID=18696787
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2000198653A Expired - Fee Related JP3968964B2 (en) | 2000-06-30 | 2000-06-30 | Steel plate for heat shrink band |
Country Status (6)
| Country | Link |
|---|---|
| US (1) | US20020139450A1 (en) |
| EP (1) | EP1310576A4 (en) |
| JP (1) | JP3968964B2 (en) |
| KR (1) | KR100468298B1 (en) |
| CN (1) | CN1196805C (en) |
| WO (1) | WO2002002838A1 (en) |
Families Citing this family (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US20050167006A1 (en) * | 2003-01-06 | 2005-08-04 | Jfe Steel Corporation | Steel sheet for high strength heat shrink band for cathode-ray tube and high strength heat shrink band |
| GB0317557D0 (en) | 2003-07-26 | 2003-08-27 | Univ Manchester | Microporous polymer material |
| CA2496212C (en) * | 2004-02-25 | 2010-01-12 | Jfe Steel Corporation | High strength cold rolled steel sheet and method for manufacturing the same |
| KR100961569B1 (en) * | 2005-02-10 | 2010-06-04 | 신닛뽄세이테쯔 카부시키카이샤 | Aluminum-based galvanized steel sheet and explosion-proof band using the same |
| CN114150211A (en) * | 2021-11-29 | 2022-03-08 | 中山市中圣金属板带科技有限公司 | Production method of steel plate for electromagnetic shielding and steel plate for electromagnetic shielding |
Family Cites Families (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2925598B2 (en) * | 1989-10-27 | 1999-07-28 | 川崎製鉄株式会社 | Material for shadow mask with excellent etching and workability |
| JPH06145797A (en) * | 1992-10-29 | 1994-05-27 | Nippon Steel Corp | Manufacturing method of electromagnetic thick plate for magnetic shield structure |
| JP3446275B2 (en) * | 1993-12-28 | 2003-09-16 | Jfeスチール株式会社 | Semi-process non-oriented electrical steel sheet with low iron loss and high magnetic permeability |
| JP2998676B2 (en) * | 1997-01-27 | 2000-01-11 | 日本鋼管株式会社 | High workability high silicon steel sheet manufactured by Si diffusion and infiltration treatment method |
| JP3987888B2 (en) * | 1997-01-29 | 2007-10-10 | ソニー株式会社 | Steel plate for heat shrink band, method for producing the same, heat shrink band and cathode ray tube device equipped with the same |
| JP3348398B2 (en) * | 1997-11-21 | 2002-11-20 | 新日本製鐵株式会社 | Cold rolled steel sheet for TV CRT shrink band |
| JP3627840B2 (en) * | 1998-05-08 | 2005-03-09 | Jfeスチール株式会社 | Steel plate for TV mask frame |
| JP3852227B2 (en) * | 1998-10-23 | 2006-11-29 | Jfeスチール株式会社 | Non-oriented electrical steel sheet and manufacturing method thereof |
| US6436199B1 (en) * | 1999-09-03 | 2002-08-20 | Kawasaki Steel Corporation | Non-oriented magnetic steel sheet having low iron loss and high magnetic flux density and manufacturing method therefor |
-
2000
- 2000-06-30 JP JP2000198653A patent/JP3968964B2/en not_active Expired - Fee Related
-
2001
- 2001-06-13 EP EP01941027A patent/EP1310576A4/en not_active Withdrawn
- 2001-06-13 WO PCT/JP2001/005002 patent/WO2002002838A1/en not_active Ceased
- 2001-06-13 CN CNB018014569A patent/CN1196805C/en not_active Expired - Fee Related
- 2001-06-13 KR KR10-2002-7001360A patent/KR100468298B1/en not_active Expired - Fee Related
-
2002
- 2002-01-24 US US10/056,153 patent/US20020139450A1/en not_active Abandoned
Also Published As
| Publication number | Publication date |
|---|---|
| US20020139450A1 (en) | 2002-10-03 |
| KR100468298B1 (en) | 2005-01-27 |
| CN1196805C (en) | 2005-04-13 |
| KR20020044133A (en) | 2002-06-14 |
| CN1380912A (en) | 2002-11-20 |
| EP1310576A4 (en) | 2005-06-29 |
| WO2002002838A1 (en) | 2002-01-10 |
| EP1310576A1 (en) | 2003-05-14 |
| JP2002012942A (en) | 2002-01-15 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| RU2109839C1 (en) | Cold-rolled steel sheet for shadow mask and method for its production | |
| JP2022513132A (en) | Aluminum-iron alloy plated steel sheets for hot forming with excellent corrosion resistance and heat resistance, hot press-formed members, and manufacturing methods thereof. | |
| JPH05214492A (en) | Fe-Ni alloy having excellent adhesion seizure prevention property and gas emission property during annealing, and method for producing the same | |
| JP3968964B2 (en) | Steel plate for heat shrink band | |
| JP3720185B2 (en) | Copper-plated steel sheet for double-wound pipes excellent in copper penetration resistance and workability, etc. and method for producing the same | |
| JPH09227998A (en) | Cold rolled steel sheet for color picture tube color separating electrode structural body and its production | |
| EP1335034A1 (en) | Low-carbon steel sheet for mask of tension type cathode ray tube with bridge and mask and cathode ray tube | |
| JP3756833B2 (en) | CRT inner frame, ferritic stainless steel plate therefor, and manufacturing method thereof | |
| WO2001012863A1 (en) | Steel sheet for heat shrink band and method for producing the same | |
| JP3892312B2 (en) | Method for manufacturing high-strength steel sheet for CRT frame | |
| US6641682B1 (en) | Method for manufacturing an aperture grill material for color picture tube | |
| KR102451003B1 (en) | High strength hot-dip galvanized steel sheet having exceelent coating adhesion and spot weldability and method of manufacturing the same | |
| JP2000256786A (en) | Cold rolled steel sheet with small in-plane anisotropy and excellent bake hardenability and aging resistance | |
| JP3775215B2 (en) | Magnetic shield material, steel plate for magnetic shield material and method for producing the same | |
| JP2003221648A (en) | High-strength hot-rolled steel sheet for picture tube frame, method for producing same, and picture tube frame | |
| JPS60255924A (en) | Manufacture of steel plate used for magnetic shielding member | |
| JP3339343B2 (en) | Manufacturing method of high workability soft hot rolled steel sheet | |
| JP3146939B2 (en) | Steel sheet with excellent blackening properties | |
| JP3360033B2 (en) | Fe-Ni alloy for shadow mask and method for producing the same | |
| JP2004059937A (en) | Material for magnetic shield for color picture tube, its manufacturing method, magnetic shielding material for color picture tube, and color picture tube | |
| JP2000169945A (en) | Material for inner shield and its production | |
| JPH08269569A (en) | Rpoduction of steel sheet stock for aperture grill | |
| JP3007662B2 (en) | Manufacturing method of hot rolled mild steel sheet with excellent longitudinal crack resistance | |
| JP2001240946A (en) | High strength heat shrink band steel sheet excellent in geomagnetic shielding properties and method of manufacturing the same | |
| JP3741246B2 (en) | Steel plate for TV mask frame |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| RD01 | Notification of change of attorney |
Free format text: JAPANESE INTERMEDIATE CODE: A7421 Effective date: 20060921 |
|
| A131 | Notification of reasons for refusal |
Free format text: JAPANESE INTERMEDIATE CODE: A131 Effective date: 20061205 |
|
| A131 | Notification of reasons for refusal |
Free format text: JAPANESE INTERMEDIATE CODE: A131 Effective date: 20070220 |
|
| A521 | Request for written amendment filed |
Free format text: JAPANESE INTERMEDIATE CODE: A523 Effective date: 20070413 |
|
| 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: 20070515 |
|
| A61 | First payment of annual fees (during grant procedure) |
Free format text: JAPANESE INTERMEDIATE CODE: A61 Effective date: 20070528 |
|
| R150 | Certificate of patent or registration of utility model |
Free format text: JAPANESE INTERMEDIATE CODE: R150 |
|
| LAPS | Cancellation because of no payment of annual fees |