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JPH05239587A - Ticn-based cermet alloy - Google Patents

Ticn-based cermet alloy

Info

Publication number
JPH05239587A
JPH05239587A JP4075298A JP7529892A JPH05239587A JP H05239587 A JPH05239587 A JP H05239587A JP 4075298 A JP4075298 A JP 4075298A JP 7529892 A JP7529892 A JP 7529892A JP H05239587 A JPH05239587 A JP H05239587A
Authority
JP
Japan
Prior art keywords
ticn
based cermet
cermet alloy
binder phase
alloy
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
Application number
JP4075298A
Other languages
Japanese (ja)
Inventor
Yusuke Iyori
裕介 井寄
Nobuhiko Shima
順彦 島
Toshinao Takahashi
利尚 高橋
Susumu Toyoda
進 豊田
Akio Washimi
暁夫 鷲見
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.)
Moldino Tool Engineering Ltd
Original Assignee
Hitachi Tool Engineering Ltd
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 Hitachi Tool Engineering Ltd filed Critical Hitachi Tool Engineering Ltd
Priority to JP4075298A priority Critical patent/JPH05239587A/en
Publication of JPH05239587A publication Critical patent/JPH05239587A/en
Pending legal-status Critical Current

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  • Cutting Tools, Boring Holders, And Turrets (AREA)

Abstract

PURPOSE:To obtain a TiCN-based cermet alloy having both high strength and high toughness by specifying the amts. of Ti, W and Mo and the ratio among them allowed to enter into solid soln. in a binding phase in a TiCN-based cermet alloy. CONSTITUTION:When a TiCN-based cermet alloy is produced by substituting one or more kinds of carbides or carbonitrides of groups IVa, Va and VIa metals other than Ti for part of TiCN as a base and carrying out bonding with an Fe family metal, the amts. of W, Mo and Ti allowed to enter into solid soln. in the binding phase are regulated so as to satisfy conditions represented by Ti+W+Mo>=6.0 and (W+Mo)/Ti>=1.0 in the case where the amt. of the binding phase is expressed as 100. The objective TiCN-based cermet alloy having remarkably improved heat resistance, especially toughness at high temp. while maintaining the same hardness is obtd.

Description

【発明の詳細な説明】Detailed Description of the Invention

【0001】[0001]

【産業上の利用分野】発明は、炭窒化チタン(以後「T
iCN」と言う)基サーメット合金に関し、特に結合相
を強化することにより高強度、高靱性を兼備したTiC
N基サーメット合金に関するものである。
BACKGROUND OF THE INVENTION The invention relates to titanium carbonitride (hereinafter referred to as "T
iCN ")-based cermet alloy, especially TiC that has both high strength and high toughness by strengthening the binder phase.
It relates to an N-based cermet alloy.

【0002】[0002]

【従来の技術】現在、窒素を含有する炭窒化チタン(以
後、TiCNと記す)基合金が工具用サーメット合金と
して主流をなしている。このTiCN基サーメット合金
は、従来のTiC基サーメット合金、超硬合金に比べ、
室温強度、耐酸化性、ならびに切削性能が改良されてい
る。
2. Description of the Related Art At present, a nitrogen-containing titanium carbonitride (hereinafter referred to as TiCN) base alloy is mainly used as a cermet alloy for tools. This TiCN-based cermet alloy, compared to the conventional TiC-based cermet alloy and cemented carbide,
Room temperature strength, oxidation resistance, and cutting performance are improved.

【0003】TiCN基サーメット合金はともに芯部
(TiW)C、(TiWTa)CNとこれを取り囲む周
辺組織(それぞれ(TiWTa)C、(TiWTa)C
Nからなる有芯構造の粒子により硬質相を形成し、強度
を向上させ、TiCN基サーメット合金は粒子径が窒素
含有によって微細化されている。さらにTiCN基サー
メット合金は、複炭窒化物中にZr、Hf等を固溶させ
ることにより、優れた高温強度を有することなども知ら
れている。
Both of the TiCN-based cermet alloys have a core (TiW) C, (TiWTa) CN and surrounding structures ((TiWTa) C and (TiWTa) C, respectively.
The core phase particles of N form a hard phase to improve the strength, and the TiCN-based cermet alloy has a fine particle size due to the nitrogen content. Further, it is also known that the TiCN-based cermet alloy has excellent high temperature strength by solid solution of Zr, Hf, etc. in the double carbonitride.

【0005】[0005]

【発明が解決しようとする問題点】以上のようにTiC
N基サーメット合金はTiC基サーメット、超硬等に比
較し硬質相は優れた特性を有しているが、結合相に関し
ては超硬の延長線上にありCo、Ni等に濡れ性を改善
するためMoを添加するか、または金属間化合物を分散
させることが行われている程度である。そのため結合相
の強化、とくに結合相の組成にに着目し、強度とくに耐
熱的特性を向上させるべき検討を行った。
Problems to be Solved by the Invention As described above, TiC
N-based cermet alloys have superior characteristics in hard phase compared to TiC-based cermets and cemented carbides, but the binder phase is on the extension line of cemented carbide to improve wettability to Co, Ni, etc. To the extent that Mo is added or an intermetallic compound is dispersed. Therefore, we focused on the strengthening of the binder phase, especially the composition of the binder phase, and conducted studies to improve the strength, especially the heat resistance.

【0006】この耐熱性については、物性とくに高温強
度に大きく影響し、クリープ試験、切削試験等に於いて
現れる。クリープ試験は高温、応力下において塑性変形
を起こしにくくし、この現象はある程度の高速切削を行
う場合に相関する。そのため本発明は、TiCN基サー
メット合金の結合相に着目しその強化を計ることによ
り、高温での靱性を向上させるとともに、特に優れた硬
さを有するTiCN基サーメット合金の提供を目的とす
る。
This heat resistance greatly affects the physical properties, especially the high temperature strength, and appears in the creep test, cutting test and the like. The creep test makes it difficult for plastic deformation to occur under high temperature and stress, and this phenomenon correlates with high-speed cutting to some extent. Therefore, an object of the present invention is to provide a TiCN-based cermet alloy that has particularly excellent hardness while improving the toughness at high temperatures by paying attention to the binder phase of the TiCN-based cermet alloy and measuring its strengthening.

【0007】[0007]

【問題を解決するための手段】結合相の強化には、Mo
の固溶量を増加させれば容易であることは当業者で有れ
ば周知の事柄であるが、TiCN基サーメット合金の場
合、特に高速切削に対応するような用途には耐熱性に優
れるW固溶量を増加させることができないことには、耐
熱性を向上させることが出来ない。
[Means for Solving the Problems] To strengthen the binder phase, Mo is used.
It is well known by those skilled in the art that it is easy to increase the solid solution amount of W. However, in the case of TiCN-based cermet alloy, W which has excellent heat resistance is used especially for applications corresponding to high speed cutting. If the amount of solid solution cannot be increased, heat resistance cannot be improved.

【0008】そこで本発明者は、TICNを基とし、そ
の一部をTiを除く4a、5a、6a族の炭化物または
炭窒化物1種または2種以上で置換し、Fe族金属で結
合して成るTiCN基サーメット合金において、結合相
に固溶されるためのW供給源を炭化物(WC)、複炭化
物、金属Wとすることについて詳細な検討を行った結
果、結合相中のW固溶量は増加させるには、単に結合相
中のW固溶量が増加するのみではなく、W、Mo、Ti
の固溶量と所定の関係にある場合に結合相強化が図ら
れ、その結果TiCN基サーメット合金の強度、特に熱
的な強度が改善することができることがわかった。
Therefore, the present inventor has substituted a part of a TICN-based carbide or carbonitride of the 4a, 5a, and 6a groups excluding Ti with one or two or more kinds, and bonding with a Fe group metal. In a TiCN-based cermet alloy consisting of the following, as a result of a detailed study on the use of carbide (WC), double carbide, and metal W as the W supply source for forming a solid solution in the binder phase, the solid solution amount of W in the binder phase In order to increase W, not only the solid solution amount of W in the binder phase increases, but W, Mo, Ti
It has been found that the binder phase is strengthened when it has a predetermined relationship with the solid solution amount of, and as a result, the strength, particularly the thermal strength, of the TiCN-based cermet alloy can be improved.

【0009】本発明者はこの知見に基づきなされたもの
で、TiCNを主体とする硬質相及びCo、Ni等から
なる結合相とからなり、結合相中Ti、WおよびMo含
有量が 6.0≦Ti+W+Mo 1.0≦(W+Mo)/Ti の条件を満足することを特徴とするTiCN基サーメッ
ト合金である。以下数値限定した理由について詳細に説
明する。
The present inventor has been made on the basis of this finding, and comprises a hard phase mainly composed of TiCN and a binder phase composed of Co, Ni, etc., and the Ti, W and Mo contents in the binder phase are 6.0. The TiCN-based cermet alloy is characterized by satisfying the condition of ≦ Ti + W + Mo 1.0 ≦ (W + Mo) / Ti. The reason for limiting the numerical values will be described in detail below.

【0010】本発明において、結合相中のTi、Wおよ
びMo含有量が6wt%以上とするのは、結合相強化の
ために最低限必要な量だからである。ここで、Ti、W
およびMo含有量は、結合相中における重量%であり、
後述の実施例で詳述するICP(inductivel
y coupled plasma)発光分析法により
求めることができる。
In the present invention, the content of Ti, W and Mo in the binder phase is 6 wt% or more because it is the minimum amount necessary for strengthening the binder phase. Where Ti, W
And Mo content are% by weight in the binder phase,
ICP (inductive) which will be described in detail in the examples below.
y coupled plasma) optical emission spectrometry.

【0011】優れた靱性、硬さを兼備するためには、結
合相中TiおよびMo含有量の総量を上記範囲とするだ
けでなく、W、MoとTiの量比が1.0≦W+Mo/
Tiの条件を満足する必要がある。それは、後述の実施
例で示すように1.0未満では靱性の改善が図れないか
らである。結合相は、CoおよびNiの1種または2種
を主体とし、その強化元素として硬質相の構成元素であ
るTi、W、Mo、Zr、Hf及び不可避不純物を含有
する。
In order to have both excellent toughness and hardness, not only the total content of Ti and Mo in the binder phase is set within the above range, but also the W, Mo and Ti content ratio is 1.0≤W + Mo /
It is necessary to satisfy the Ti condition. This is because the toughness cannot be improved when the ratio is less than 1.0 as shown in Examples described later. The binder phase is mainly composed of one or two of Co and Ni, and contains Ti, W, Mo, Zr, Hf, which are the constituent elements of the hard phase, and unavoidable impurities as its strengthening elements.

【0012】[0012]

【実施例】配合に使用した原料は市販のTiCN粉末
(平均粒度1.0μm) 、WC粉末(同1.0μm)
、TaC粉末(同1.0μm) 、また上記粉末を使用
してWC−TiC−TiN−TaCの固溶体を作成し
た。固溶体は WC/TiC/TiN /Ta=2/3
/3/2となるよう配合し、乾燥後、1600℃ 2時
間、N雰囲気中で固溶化処理し、粒度調整を行い、平均
粒度0.8μmの粉末を作成した。
[Examples] The raw materials used for blending were commercially available TiCN powder (average particle size 1.0 μm) and WC powder (1.0 μm).
, TaC powder (1.0 μm in the same), and a solid solution of WC-TiC-TiN-TaC was prepared using the above powder. The solid solution is WC / TiC / TiN / Ta = 2/3
It was blended so as to be ⅔ / 2, dried and then subjected to solution treatment at 1600 ° C. for 2 hours in an N atmosphere to adjust the particle size to prepare a powder having an average particle size of 0.8 μm.

【0013】これらの粉末を表1に示す様に種々な組成
で混合し、乾燥し、TEE433のスローアウェイチッ
プをプレス成形し、真空中1500℃1hr 焼結した
のち、所定の形状に加工した。なお固溶体はTa量を基
本としTi、WはTiCN、TiC、TiN、WC等を
用いて添加した。
As shown in Table 1, these powders were mixed in various compositions, dried, and press-molded with a throw away tip of TEE433, sintered at 1500 ° C. for 1 hr in vacuum, and then processed into a predetermined shape. The solid solution was based on the amount of Ta, and Ti and W were added by using TiCN, TiC, TiN, WC, or the like.

【0014】次に物性を確認するため上記チップを研
磨、ラップした後、ビッカース硬度、靱性を表すクラッ
ク抵抗(kg/mm)、結合相中の元素の固溶量(結合
相中の溶解量を100%として求めた)を求めた。ビッ
カース硬度は、JIS規格に準じダイアモンド圧子で3
0kgの荷重をかけ、対角線長さを測定し硬度換算表よ
り求めた。クラック抵抗(kg/mm)は、ビッカース
硬度と同じ様にダイアモンド圧子で50kgの荷重をか
け、圧痕の4角に生ずるクラックの距離を計り、荷重/
クラックの長さの和 により求めた。
Next, after polishing and lapping the above chips to confirm the physical properties, Vickers hardness, crack resistance (kg / mm) indicating toughness, solid solution amount of elements in the binder phase (dissolved amount in the binder phase, It was calculated as 100%). Vickers hardness is 3 with diamond indenter according to JIS standard
A load of 0 kg was applied and the diagonal length was measured and determined from the hardness conversion table. The crack resistance (kg / mm) is determined by applying a load of 50 kg with a diamond indenter as in the Vickers hardness and measuring the distance of cracks generated at the four corners of the indentation.
It was calculated by summing the lengths of cracks.

【0015】結合相中の元素固溶量は、結合相を混酸水
溶液で溶解、抽出し、ICP(inductively
coupled plasma)発光分析法によって
結合相中の各元素を定量することにより求めた。表2に
ビッカーズ硬度、靱性をクラック抵抗(kg/mm)、
結合相中のTi+W+Mo量(wt%)、Mo+W/T
iを示す。さらに下記の切削諸元により試験を行った。 切削速度 200m/min 送り 0.08mm/刃 切込み 1.0mm 被削材 SCM440 チップ形状 TEE433 カッター形状 φ80 1枚刃 その結果を表3に示す。切削試験は、切削時のヒートサ
イクルにより生ずる熱亀裂より、チッヒ゜ンク゛に至るまでの
摩耗量と時間を測定した。
The amount of elemental solid solution in the binder phase is determined by dissolving and extracting the binder phase with an aqueous mixed acid solution, and measuring ICP (inductively).
It was determined by quantifying each element in the binding phase by coupled plasma emission spectrometry. Table 2 shows Vickers hardness and toughness, crack resistance (kg / mm),
Ti + W + Mo content (wt%) in binder phase, Mo + W / T
indicates i. Further, a test was conducted according to the following cutting specifications. Cutting speed 200 m / min Feed 0.08 mm / blade Cutting 1.0 mm Work material SCM440 Tip shape TEE433 Cutter shape φ80 1-blade The results are shown in Table 3. In the cutting test, the amount of wear and the time required to reach chipping from the thermal crack generated by the heat cycle during cutting were measured.

【0016】[0016]

【表1】 試番 TiC TiN WC TaC Mo Co Ni 本発明例 1 27.0 27.0 21.0 10.0 - 7.5 7.5 本発明例 2 27.0 27.0 19.0 10.0 2.0 7.5 7.5 本発明例 3 27.0 27.0 16.0 10.0 5.0 7.5 7.5 本発明例 4 40.5 13.5 16.0 10.0 5.0 7.5 7.5 本発明例 5 40.5 13.5 16.0 10.0 5.0 7.5 7.5 比較例 6 35.0 35.0 - 10.0 5.0 7.5 7.5[Table 1] Sample number TiC TiN WC TaC Mo Co Co Ni Present invention example 1 27.0 27.0 21.0 10.0-7.5 7.5 Present invention example 2 27.0 27.0 19.0 10.0 2.0 7.5 7.5 Present invention example 3 27.0 27.0 16.0 10.0 5.0 7.5 7.5 Present invention example 4 40.5 13.5 16.0 10.0 5.0 7.5 7.5 Inventive Example 5 40.5 13.5 16.0 10.0 5.0 7.5 7.5 Comparative Example 6 35.0 35.0-10.0 5.0 7.5 7.5

【0017】[0017]

【表2】 試番 サーメットの結合相分布(WT%) W+Mo Ti+Mo+W (W+Mo)/Ti 硬さ クラック抵 抗 Ti W Mo Co Ni Hv Kg/mm 1 3.0 3.5 - 46 bal 3.5 6.5 1.1 1420 105 2 3.2 2.3 4.4 45 bal 5.5 9.9 3.1 1460 102 3 2.3 1.7 6.0 45 bal 4.0 10.0 1.7 1460 110 4 1.2 1.5 5.5 46 bal 7.0 8.2 5.8 1490 113 5 1.2 1.0 4.8 46 bal 5.8 7.0 4.8 1490 102 6 1.0 - 4.0 47 bal 5.0 7.0 2.5 1410 105[Table 2] Bonded phase distribution (WT%) of the sample number Cermet W + Mo Ti + Mo + W (W + Mo) / Ti hardness Crack resistance Ti W Mo Co Ni Hv Kg / mm 1 3.0 3.5-46 bal 3.5 6.5 1.1 1420 105 2 3.2 2.3 4.4 45 bal 5.5 9.9 3.1 1460 102 3 2.3 1.7 6.0 45 bal 4.0 10.0 1.7 1460 110 4 1.2 1.5 5.5 46 bal 7.0 8.2 5.8 1490 113 5 1.2 1.0 4.8 46 bal 5.8 7.0 4.8 1490 102 6 1.0-4.0 47 bal 5.0 7.0 2.5 1410 105

【0018】[0018]

【表3】 試番 切削時間(min) 逃げ面最大摩耗量 備考 1 45 0.38 2 40 0.29 3 45 0.31 4 50 0.32 5 38 0.38 6 20 0.05 切り刃脱落あり[Table 3] Trial No. Cutting time (min) Maximum flank wear amount Remarks 1 45 0.38 2 40 0.29 3 45 0.31 4 50 0.32 5 38 0.38 6 20 0.05 Cutting edge removal Yes

【0019】表3の結果より、比較サーメットではチッ
ピングを生じた後、欠損に至り寿命となったのに対し、
本発明サーメットでは超硬合金P系と同様、ある程度、
欠損を生ぜずに熱疲労亀裂が発生しても切削が可能であ
った。また、これらの切削試験において、本発明例は欠
損が生じにくい為長寿命化が達成された。
From the results of Table 3, in the comparative cermet, after chipping occurred, chipping occurred and the life reached.
In the cermet of the present invention, similar to the cemented carbide P system,
It was possible to cut even if a thermal fatigue crack occurred without causing defects. In addition, in these cutting tests, the examples of the present invention were less prone to chipping, so that a longer life was achieved.

【0020】[0020]

【発明の効果】以上のように、本発明によるTiCN基
サーメット合金は結合相中のTi、W、Moの固溶量と
その比率を特定することにより、同等の硬さを有しつつ
耐熱性とくに高温での靱性を著しく改善したTiCN基
サーメット合金を得ることができ、切削においても優れ
た性能を示した。
As described above, the TiCN-based cermet alloy according to the present invention has the same hardness and heat resistance by specifying the solid solution amounts of Ti, W and Mo in the binder phase and their ratios. In particular, a TiCN-based cermet alloy with significantly improved toughness at high temperatures could be obtained, and excellent performance was exhibited in cutting.

フロントページの続き (72)発明者 豊田 進 千葉県成田市新泉13番地の2 日立ツール 株式会社成田工場内 (72)発明者 鷲見 暁夫 千葉県成田市新泉13番地の2 日立ツール 株式会社成田工場内Front Page Continuation (72) Inventor Susumu Toyota Susumu Narita, Chiba Prefecture 2 13 Narita Factory Hitachi Tool Co., Ltd. (72) Inventor Akio Washi 13 Narita Chiba Prefecture 2 Niizumi Hitachi Tool Co., Ltd. Narita Factory

Claims (1)

【特許請求の範囲】[Claims] 【請求項1】 TiCNを基とし、その一部をTiを除
く4a、5a、6a族の炭化物または炭窒化物1種また
は2種以上で置換し、Fe族金属で結合して成るTiC
N基サーメット合金において、結合相に固溶されるW、
Mo、Tiの固溶量が、結合相を100とした時に 6.0≦Ti+W+Mo 1.0≦(W+Mo)/Ti の条件を満足することを特徴とするTiCN基サーメッ
ト合金。
1. TiC based on TiCN, part of which is replaced by one or more of 4a, 5a, and 6a carbides or carbonitrides other than Ti, and bonded with an Fe group metal.
In an N-based cermet alloy, W dissolved in the binder phase,
A TiCN-based cermet alloy, characterized in that the solid solution amounts of Mo and Ti satisfy the condition of 6.0 ≦ Ti + W + Mo 1.0 ≦ (W + Mo) / Ti when the binder phase is 100.
JP4075298A 1992-02-26 1992-02-26 Ticn-based cermet alloy Pending JPH05239587A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP4075298A JPH05239587A (en) 1992-02-26 1992-02-26 Ticn-based cermet alloy

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP4075298A JPH05239587A (en) 1992-02-26 1992-02-26 Ticn-based cermet alloy

Publications (1)

Publication Number Publication Date
JPH05239587A true JPH05239587A (en) 1993-09-17

Family

ID=13572206

Family Applications (1)

Application Number Title Priority Date Filing Date
JP4075298A Pending JPH05239587A (en) 1992-02-26 1992-02-26 Ticn-based cermet alloy

Country Status (1)

Country Link
JP (1) JPH05239587A (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2008183708A (en) * 1995-11-30 2008-08-14 Sandvik Intellectual Property Ab Coated insert for milling and its manufacturing method
US8497340B2 (en) 2006-06-21 2013-07-30 Daikin Industries, Ltd. Fluorosilicone mold release composition

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2008183708A (en) * 1995-11-30 2008-08-14 Sandvik Intellectual Property Ab Coated insert for milling and its manufacturing method
US8497340B2 (en) 2006-06-21 2013-07-30 Daikin Industries, Ltd. Fluorosilicone mold release composition

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