JP2857116B2 - Automatic welding support - Google Patents

Automatic welding support

Info

Publication number
JP2857116B2
JP2857116B2 JP9041974A JP4197497A JP2857116B2 JP 2857116 B2 JP2857116 B2 JP 2857116B2 JP 9041974 A JP9041974 A JP 9041974A JP 4197497 A JP4197497 A JP 4197497A JP 2857116 B2 JP2857116 B2 JP 2857116B2
Authority
JP
Japan
Prior art keywords
weight
base material
welding
glass fiber
ceramic base
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 - Lifetime
Application number
JP9041974A
Other languages
Japanese (ja)
Other versions
JPH1024395A (en
Inventor
武 秀 鄭
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.)
Individual
Original Assignee
Individual
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Filing date
Publication date
Application filed by Individual filed Critical Individual
Publication of JPH1024395A publication Critical patent/JPH1024395A/en
Application granted granted Critical
Publication of JP2857116B2 publication Critical patent/JP2857116B2/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Classifications

    • BPERFORMING OPERATIONS; TRANSPORTING
    • B23MACHINE TOOLS; METAL-WORKING NOT OTHERWISE PROVIDED FOR
    • B23KSOLDERING OR UNSOLDERING; WELDING; CLADDING OR PLATING BY SOLDERING OR WELDING; CUTTING BY APPLYING HEAT LOCALLY, e.g. FLAME CUTTING; WORKING BY LASER BEAM
    • B23K37/00Auxiliary devices or processes, not specially adapted to a procedure covered by only one of the preceding main groups
    • B23K37/06Auxiliary devices or processes, not specially adapted to a procedure covered by only one of the preceding main groups for positioning the molten material, e.g. confining it to a desired area
    • CCHEMISTRY; METALLURGY
    • C04CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
    • C04BLIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
    • C04B2235/00Aspects relating to ceramic starting mixtures or sintered ceramic products
    • C04B2235/70Aspects relating to sintered or melt-casted ceramic products
    • C04B2235/96Properties of ceramic products, e.g. mechanical properties such as strength, toughness, wear resistance
    • C04B2235/9607Thermal properties, e.g. thermal expansion coefficient
    • CCHEMISTRY; METALLURGY
    • C04CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
    • C04BLIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
    • C04B35/00Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products
    • C04B35/01Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products based on oxide ceramics
    • C04B35/14Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products based on oxide ceramics based on silica
    • CCHEMISTRY; METALLURGY
    • C04CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
    • C04BLIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
    • C04B38/00Porous mortars, concrete, artificial stone or ceramic ware; Preparation thereof
    • C04B38/0051Porous mortars, concrete, artificial stone or ceramic ware; Preparation thereof characterised by the pore size, pore shape or kind of porosity

Description

【発明の詳細な説明】DETAILED DESCRIPTION OF THE INVENTION

【0001】[0001]

【発明の属する技術分野】本発明は、自動溶接用支持具
に関し、特に母材補助具としてガラス繊維体が母材面に
積層された、母材材質が改善された自動溶接用支持具に
関する。
BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a support for automatic welding, and more particularly, to a support for automatic welding in which a glass fiber body is laminated on a base material surface as a base material auxiliary tool and the material of the base material is improved.

【0002】[0002]

【従来の技術】一般に自動溶接は、高電流(850〜
1,250A)、高電圧で行われる溶接手法であり、セ
ラミックス製溶接用支持具の母材自体は耐熱性及び耐熱
衝撃性に優れていることが望ましい。
2. Description of the Related Art Generally, automatic welding is performed at a high current (850 to 850).
1,250 A), which is a welding method performed at a high voltage, and it is desirable that the base material of the ceramic welding support has excellent heat resistance and thermal shock resistance.

【0003】しかしながら、従来の自動アーク溶接用支
持具として用いられてきた、鋳物砂にフェノール樹脂を
覆い180℃前後の低温で熱硬化させた固形フラックス
には、溶接時の高熱(約1,550℃前後)により支持
具の鋳物砂を覆っているフェノール樹脂が完全に分解燃
焼するという欠点があった。
[0003] However, the solid flux which has been used as a conventional support for automatic arc welding, which is obtained by covering a phenolic resin with a casting sand and thermally hardening it at a low temperature of about 180 ° C, has a high heat during welding (about 1,550). (Approx. ° C.), the phenol resin covering the molding sand of the support tool has a disadvantage that it is completely decomposed and burned.

【0004】これにより結合力を失った鋳物砂は、溶接
後多量の粉塵を発生させる原因となり、また鋼板に固形
フラックスを取り付けるために第2図のようなマグネチ
ッククランプ2aを用いるが、これは劣悪の勤労条件に
つながり、生産性低下及び原価上昇要因となる。
[0004] The foundry sand which has lost the bonding force thereby causes a large amount of dust after welding, and a magnetic clamp 2a as shown in Fig. 2 is used to attach a solid flux to a steel sheet. This leads to poor working conditions, which leads to lower productivity and higher costs.

【0005】また固形フラックスの形状は、一個当りの
長さ(EA)600mmと完全に規格化されているので、
曲面部のように溶接が難しい部位には適用できない。
Since the shape of the solid flux is completely standardized to a length (EA) of 600 mm per piece,
It cannot be applied to parts where welding is difficult, such as curved surfaces.

【0006】[0006]

【発明が解決しようとする課題】本発明は、粉塵発生が
なく、マグネチッククランプを使用せず、曲面部溶接も
可能な自動溶接用支持具を提供することを目的とする。
SUMMARY OF THE INVENTION An object of the present invention is to provide an automatic welding support which does not generate dust, does not use a magnetic clamp, and is capable of welding a curved surface portion.

【0007】[0007]

【課題を解決するための手段】本発明の自動溶接用支持
具は、70〜95重量%のSiO2 、2〜15重量%の
Al23 、1〜5重量%のMgO、1.2〜8重量%
のNa2 O及び/またはK2 O並びに0.01〜0.5
重量%の水分を含む、気孔率25〜48%及び耐火度
1,435〜1,670℃のセラミック母材、並びに該
母材上に積層された40〜70重量%のSiO2 、5〜
20重量%のAl23 、3〜15重量%のB23
8〜28重量%のCaO、0.5〜4重量%のアルカリ
金属酸化物及び0.01〜0.5重量%の水分を含む、
厚さ0.3〜1.5mmのガラス繊維体を含むことを特徴
とする。
Automatic welding support of the present invention According to an aspect of the 70 to 95% by weight of SiO 2, 2 to 15 wt% of Al 2 0 3, 1 to 5 wt% of MgO, 1.2 ~ 8% by weight
Na 2 O and / or K 2 O and 0.01 to 0.5
A ceramic base material having a porosity of 25 to 48% and a fire resistance of 1,435 to 1,670 ° C, containing 40% by weight of water, and 40 to 70% by weight of SiO 2 ,
20 wt% of Al 2 O 3, 3~15 wt% B 2 O 3,
Comprising 8 to 28% by weight of CaO, 0.5 to 4% by weight of an alkali metal oxide and 0.01 to 0.5% by weight of water;
It is characterized by containing a glass fiber body having a thickness of 0.3 to 1.5 mm.

【0008】また、本発明の自動溶接用支持具は、前記
の母材が、石英、トリジマイト及び/またはクリストバ
ライトを含有していてもよい。
Further, in the support for automatic welding according to the present invention, the base material may contain quartz, tridymite and / or cristobalite.

【0009】[0009]

【発明の実施の形態】本発明に係るセラミック母材の主
成分であるSiO2 は、セラミック母材中に70〜95
重量%含まれる。この範囲に規定した理由は、70重量
%未満では耐熱性が低下し、過大スラグを発生してイン
ナービードを生成し、また溶解物が多いのでアーク熱が
不安定になり、アンダーカット、スパッタリングという
融点欠陥をもたらし、また95重量%を超える場合はス
ラグの流動性が少なくなるので均一のインナービードが
生成できず、スラグの剥離性が低下され、スラグの巻か
れ現象等が発生するからである。
DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENTS SiO 2 which is a main component of the ceramic base material according to the present invention contains 70 to 95% in the ceramic base material.
% By weight. The reason specified in this range is that if the content is less than 70% by weight, heat resistance is reduced, excessive slag is generated to form an inner bead, and since there is a large amount of dissolved material, arc heat becomes unstable, and the undercut and sputtering are performed. Melting point defects are caused, and when the content exceeds 95% by weight, the fluidity of the slag is reduced, so that a uniform inner bead cannot be formed, the removability of the slag is reduced, and the slag winding phenomenon occurs. .

【0010】次に、本発明に係るセラミック母材中に含
まれるAl23 の含有量は、セラミック母材の耐火度
を高めて自動溶接時の高熱に耐えられるようにし、溶接
時に生成されるスラグの粘性を高めて均一バックビード
を有するように2〜15重量%の範囲である。この範囲
に規定した理由は、2重量%未満ではスラグの剥離性が
弱く、溶接の後バックガウジングを行う必要があり、1
5重量%を超える場合は耐火度が高くなりすぎ、スラグ
の粘性が低くなりスラグの巻かれ現象であるアンダーカ
ットが発生し、またスパッタリング、オーバーラップ等
のような溶接欠陥も発生するからである。
Next, the content of Al 2 O 3 contained in the ceramic base material according to the present invention increases the fire resistance of the ceramic base material so that it can withstand high heat during automatic welding, and is generated during welding. The range is from 2 to 15% by weight to increase the viscosity of the slag and to have a uniform back bead. The reason defined in this range is that if the content is less than 2% by weight, the slag peelability is weak, and it is necessary to perform back gouging after welding.
If the content is more than 5% by weight, the fire resistance becomes too high, the viscosity of the slag becomes low, the undercut which is a slag winding phenomenon occurs, and welding defects such as sputtering and overlap also occur. .

【0011】また、本発明に係るセラミック母材中に含
まれるMgOは、作用的にはAl23 と類似する成分
であり、セラミック母材の耐熱性を高め、スラグの薄性
を良好にする成分である。ここでMgOの含有量は1〜
5重量%であり、この範囲に規定した理由は、1重量%
未満では溶融金属の粘性が低くなりスラグの剥離性が低
下し、多量のアンダーカット及びオーバーラップ等が生
じ、また5重量%を超える場合は溶融金属の粘性が過大
になりガス放出が困難になりフローフォール、スパッタ
リング、くぼみ等の溶接欠陥の発生を招くからである。
Further, MgO contained in the ceramic base material according to the present invention is a component functionally similar to Al 2 O 3, and enhances the heat resistance of the ceramic base material and improves the thinness of the slag. It is a component that does. Here, the content of MgO is 1 to
5% by weight, and the reason specified in this range is 1% by weight.
If it is less than 5%, the viscosity of the molten metal becomes low, and the slag removability decreases, and a large amount of undercut and overlap occur. If it exceeds 5% by weight, the viscosity of the molten metal becomes excessive and gas release becomes difficult. This is because welding defects such as flow fall, sputtering, and dents are caused.

【0012】次に、本発明に係るセラミック母材中に含
まれるNa2 OやK2 Oは、セラミック母材内でフラッ
クス作用とセラミック母材の塑性範囲を広げる作用をす
る成分である。ここでNa2 OやK2 Oの含有量は1.
2〜8重量%であり、この範囲に規定した理由は、1.
2重量%未満ではスラグの粘性が低くなりスラグの剥離
性が缺如し、生成されたインナービードの巻かれ現象す
なわち多量のアンダーカットという溶接欠陥が発生する
反面、8重量%を超える場合はセラミック母材をガラス
化し、急熱、急冷の際の熱衝撃抵抗性を低下させるから
である。
Next, Na 2 O or K 2 O contained in the ceramic base material according to the present invention is a component that has a flux function and a function of expanding the plastic range of the ceramic base material in the ceramic base material. Here, the content of Na 2 O or K 2 O is 1.
2 to 8% by weight, and the reason specified in this range is as follows.
If the content is less than 2% by weight, the viscosity of the slag becomes low, the slag peeling property is lacking, and the generated inner bead is wrapped, that is, a large amount of undercut occurs. This is because the base material is vitrified to reduce the thermal shock resistance during rapid heating and rapid cooling.

【0013】また、本発明に係るセラミック母材中に含
まれる水分は、0.01〜0.5重量%であるが、この
範囲に規定した理由は、セラミック母材の水分含量が溶
接時のフローホールやくぼみに大きな影響を与えるから
であり、0.5重量%を超える水分がセラミック母材内
に存在する場合には溶接時に瞬間的にセラミック母材か
らの水分を溶融金属が吸湿しバックビード内に多量の微
細気孔を発生させるからである。なお、この水分は、大
気中の水分を吸収することにより、セラミック母材表面
や気孔中に存在するものである。
The moisture contained in the ceramic base material according to the present invention is 0.01 to 0.5% by weight, but the reason specified in this range is that the water content of the ceramic base material at the time of welding is limited. This is because it has a great effect on the flow holes and depressions. If moisture exceeding 0.5% by weight is present in the ceramic base material, the molten metal absorbs moisture from the ceramic base material instantaneously during welding and backs up. This is because a large amount of fine pores are generated in the bead. The moisture is present on the surface of the ceramic base material and in the pores by absorbing moisture in the atmosphere.

【0014】次に、本発明に係るセラミック母材の気孔
率は、25〜48%である。この範囲に規定することに
より、セラミック母材の急熱や急冷による熱衝撃抵抗力
が増加し、特に溶接時にセラミック母材が破損すること
なく溶融金属の支持が可能となる。気孔率が25%未満
の場合、セラミック母材が緻密すぎてセラミックスがガ
ラス化し、ガスが容易には放出されなくなり、熱衝撃に
よりセラミックスが破損し易くなり、反対に48%以上
の場合、セラミック母材の機械的強度が低下して外部衝
撃による破損が生じる恐れがあり、大気中に存在する水
分を吸収して溶接時のバックビード内微細気孔を形成さ
せる原因となる。なお、この気孔率は、次式で定義され
る。 気孔率=(W3 −W1)/(W3 −W2)×100 (W1 :乾燥重量、W2 :水中重量、W3 :水から引き
上げたときの飽水重量)
Next, the porosity of the ceramic base material according to the present invention is 25 to 48%. By defining this range, the thermal shock resistance due to rapid heating and rapid cooling of the ceramic base material increases, and it is possible to support the molten metal without damaging the ceramic base material particularly during welding. When the porosity is less than 25%, the ceramic base material is too dense and the ceramic vitrifies, gas is not easily released, and the ceramic is liable to be damaged by thermal shock. There is a possibility that the mechanical strength of the material is reduced and the material is damaged by an external impact, and absorbs moisture existing in the atmosphere to form fine pores in the back bead during welding. The porosity is defined by the following equation. Porosity = (W 3 −W 1 ) / (W 3 −W 2 ) × 100 (W 1 : dry weight, W 2 : water weight, W 3 : saturated water weight when pulled up from water)

【0015】本発明に係るセラミック母材の耐火度は、
1,435〜1,670℃(SK15〜30番)であ
る。一般的に自動溶接は約1,550℃前後の高温で行
われるが、1,435℃(SK15番)以下の耐火度の
場合はスラグを過剰発生して溶融金属内部へセラミック
構成成分が溶入してしまうために溶接鋼の純度が低下す
る反面、1,670℃(SK30番)以上の耐火度の場
合はスラグ発生が抑制されすぎ溶接後にセラミック母材
がスラグに貼り付いて鋼から剥離せず、そのためにバッ
クガウジングという二重作業をする必要があるからであ
る。
The fire resistance of the ceramic base material according to the present invention is as follows:
1,435 to 1,670 ° C (SK15 to 30). Generally, automatic welding is performed at a high temperature of about 1,550 ° C. However, in the case of a fire resistance of 1,435 ° C or less (SK15) or less, slag is excessively generated and ceramic components penetrate into the molten metal. Although the purity of the welded steel is reduced due to this, on the other hand, in the case of a fire resistance of 1,670 ° C. (SK30) or more, the generation of slag is suppressed too much and the ceramic base material sticks to the slag after welding and peels off from the steel. This is because, for that purpose, it is necessary to perform double work called back gouging.

【0016】その他、本発明に係るセラミック母材は、
Fe23 、TiO2 、Li2 O、CaO、ZrO2
のような金属酸化物の1種以上を0.5〜5重量%含有
していてもよい。
In addition, the ceramic base material according to the present invention comprises:
Fe 2 O 3, TiO 2, Li 2 O, CaO, 1 or more may contain 0.5 to 5 wt% of a metal oxide such as ZrO 2 and the like.

【0017】本発明に係るガラス繊維体は、SiO2
含有し、その含有量は40〜70重量%である。この範
囲に規定した理由は、40重量%では耐熱性が低下し、
ガラス繊維が過大に溶融し、多量のガスが発生し、スラ
グの過剰生成によるスラグの剥離低下、フローホール、
くぼみ等の溶接欠陥の原因となり、また70重量%を超
える場合はガラス繊維の弾性が低下し、曲がり強度が著
しく低下し、ガラス繊維の破壊により溶接時のセラミッ
ク母材が溶融金属から保護されず、スラグの流動性が低
下して多量のアンダーカットやオーバーラップ等の欠陥
が発生するからである。
The glass fiber according to the present invention contains SiO 2 and its content is 40 to 70% by weight. The reason specified in this range is that the heat resistance is reduced at 40% by weight,
Glass fiber is excessively melted, and a large amount of gas is generated.
If the content exceeds 70% by weight, the elasticity of the glass fiber is reduced and the bending strength is significantly reduced. If the glass fiber is broken, the ceramic base material at the time of welding is not protected from the molten metal. This is because the fluidity of the slag decreases and a large amount of defects such as undercut and overlap occur.

【0018】次に本発明に係るガラス繊維体中に含まれ
るAl23 の含有量は、5〜20重量%である。この
範囲に規定した理由は、5重量%未満では耐熱性が低す
ぎ多量の溶融金属とスラグ生成を起こしガス放出を困難
にし、スラグの剥離低下及びフローホールのような欠陥
をもたらす反面、20重量%を超える場合はガラス繊維
体の耐火度が高すぎてスラグの流動性低下を招き、アン
ダーカットのような溶接欠陥が発生するからである。
Next, the content of Al 2 O 3 contained in the glass fiber body according to the present invention is 5 to 20% by weight. The reason specified in this range is that if the content is less than 5% by weight, the heat resistance is too low, a large amount of molten metal is generated and slag is generated, which makes gas release difficult, resulting in reduced slag separation and defects such as flow holes. %, The fire resistance of the glass fiber body is too high, which causes a decrease in the fluidity of the slag, and causes welding defects such as undercut.

【0019】また、本発明に係るガラス繊維体中に含ま
れるB23 の含有量は、3〜15重量%である。この
範囲に規定した理由は、B23 はガラス繊維内でフラ
ックス作用をしてガラス繊維の塑性範囲を広げる役割を
するが、3重量%未満ではスラグの流動性が低下してス
ラグの剥離性が缺如し、生成したインナービードの巻か
れ現象が発生する反面、15重量%を超える場合はガラ
ス繊維の曲がり強度が低下し、ガラス繊維が細砕し、バ
ックビード形状が必要以上広く深く形成され、ワイヤが
多量消耗されて原価上昇を招くからである。
The content of B 2 O 3 contained in the glass fiber according to the present invention is 3 to 15% by weight. The reason defined in this range is that B 2 O 3 has a function of expanding the plastic range of the glass fiber by performing a flux action in the glass fiber, but if it is less than 3% by weight, the fluidity of the slag is reduced and the slag is separated. Insufficiency and the resulting inner bead winding phenomenon occurs. On the other hand, if it exceeds 15% by weight, the bending strength of the glass fiber decreases, the glass fiber is crushed, and the back bead shape is wider and deeper than necessary. This is because the wires are formed and a large amount of wire is consumed, resulting in an increase in cost.

【0020】次に、本発明に係るガラス繊維体中に含ま
れるCaOの含有量は、8〜28重量%である。作用的
にはCaOはB23 と類似する成分であり、ガラス繊
維体の耐熱性、機械的強度、塑性範囲等を調節する。こ
こで、含有量をこの範囲に規定した理由は、8重量%未
満ではスラグの流動性が低下し、スラグの剥離性が缺如
し、インナービード巻かれ現象によってアンダーカット
が発生する等の溶接欠陥を招く反面、28重量%を超え
る場合は耐火度が低くなるため溶融物が過大となりスラ
グが過剰生成してガスが大量発生し、そのガスの一部が
水分と化学反応を起こして溶接後にビード内に気泡をも
たらし、致命的な溶接欠陥を招くからである。
Next, the content of CaO contained in the glass fiber body according to the present invention is 8 to 28% by weight. Functionally, CaO is a component similar to B 2 O 3 and regulates the heat resistance, mechanical strength, plastic range, etc. of the glass fiber body. Here, the reason why the content is specified in this range is that if the content is less than 8% by weight, the fluidity of the slag is reduced, the peelability of the slag is lacking, and the undercut is generated due to the inner bead winding phenomenon. On the other hand, when the content exceeds 28% by weight, the refractory becomes low and the melt becomes excessively large, the slag is excessively generated and a large amount of gas is generated when the content exceeds 28% by weight. This is because air bubbles are generated in the bead, resulting in fatal welding defects.

【0021】また、本発明に係るガラス繊維体は、Na
2 O、K2 O、Li2 Oのアルカリ金属酸化物を含有し
ていてもよく、好ましくはその含有量は0.5〜4重量
%である。アルカリ金属酸化物は、ガラス繊維の引張強
度、圧縮強度、曲がり強度等のような機械的性質及び成
形性に関して重要な成分である。
Further, the glass fiber according to the present invention comprises Na
It may contain an alkali metal oxide of 2 O, K 2 O, or Li 2 O, and its content is preferably 0.5 to 4% by weight. Alkali metal oxides are important components for mechanical properties such as tensile strength, compressive strength, bending strength and the like of glass fibers and moldability.

【0022】次に、本発明に係るガラス繊維体の水分含
有量は、0.01〜0.5重量%である。この範囲に規
定した理由は、水分含有量はセラミック母材と同様に溶
接欠陥に影響を及ぼすが、0.5重量%を超える場合は
溶接時のバックビード内に多量の水分が浸透し、溶接
後、ビード内に多量の微細気孔が発生するからである。
なお、この水分は、大気中の水分を吸収することによ
り、ガラス繊維体表面や気孔(繊維組織間を含む)中に
存在するものである。
Next, the water content of the glass fiber according to the present invention is 0.01 to 0.5% by weight. The reason specified in this range is that the water content affects welding defects as in the case of the ceramic base material, but if it exceeds 0.5% by weight, a large amount of water permeates into the back bead during welding, Later, a large amount of fine pores are generated in the bead.
The moisture is present on the surface of the glass fiber body and in the pores (including between fiber tissues) by absorbing moisture in the atmosphere.

【0023】また、本発明に係るガラス繊維体の厚さ
は、0.3〜1.5mmであるのが好ましい。ガラス繊維
体はアーク熱により発生するガスの放出を容易にし、溶
接欠陥を防ぐ役割をするが、その際、ガラス繊維の厚さ
により作用効果が異なる。0.3mm以下の場合は鋼とセ
ラミック母材との緩衝作用が得られず、また、溶接の際
早い段階で溶融してしまいセラミック母材の露出及びガ
ス放出が困難となり、バックビード内にくぼみが露出し
スラグの剥離を低下させる反面、1.5mmを超える場合
はガス放出が容易となるが、厚すぎるため、溶接後、ガ
ラス繊維がセラミック母材上に残存し、バックビードの
広さ及び深さ等の調節が困難になる。
The thickness of the glass fiber according to the present invention is preferably 0.3 to 1.5 mm. The glass fiber body facilitates the release of gas generated by the arc heat and prevents welding defects. At this time, the effect differs depending on the thickness of the glass fiber. If the thickness is less than 0.3 mm, the buffering effect between the steel and the ceramic base material cannot be obtained, and it will melt at an early stage during welding, making it difficult to expose the ceramic base material and release gas, and to dent in the back bead. While exposing and lowering the slag peeling, if it exceeds 1.5 mm, outgassing becomes easy, but because it is too thick, the glass fiber remains on the ceramic base material after welding, and the width of the back bead and It becomes difficult to adjust the depth and the like.

【0024】また、このガラス繊維体は、ガラス繊維を
1重または多重にしたものでもよい。
The glass fiber body may be a single or multiple glass fiber.

【0025】次に、本発明に係るセラミック母材の製造
方法を説明する。先ず、使用する原料は、例えば60〜
80メッシュの粒度分布を有するα−石英、トリジマイ
トやクリストバライトを用いる。また、天然のこれら鉱
物は、SiO2 、Al23 、MgO、Na2 O、Fe
23 、TiO2 、Li2 OやZrO2 等を含有してい
るものもあるので、この場合はこれらを利用すれば準備
すべき原料の種類が減り好ましい。
Next, a method of manufacturing a ceramic base material according to the present invention will be described. First, the raw materials used are, for example, 60 to
Α-quartz, tridymite or cristobalite having a particle size distribution of 80 mesh is used. In addition, these natural minerals include SiO 2 , Al 2 O 3 , MgO, Na 2 O, Fe
Some of them contain 2 O 3 , TiO 2 , Li 2 O, ZrO 2, etc. In this case, it is preferable to use these materials because the types of raw materials to be prepared are reduced.

【0026】また、各成分に対応した複数の原料を用い
てもよい。例えば、SiO2 源として、シリカ、カオリ
ン、長石、雲母、滑石、ムライト等、Al23 源とし
て、アルミナ、カオリン、ムライト、ボーキサイト等、
MgO源として、コージェライト、酸化マグネシウム、
滑石等、Na2 O源として、ソーダ長石、酸化ナトリウ
ム、水ガラス等、K2 O源として、カリ長石、チタン酸
カルシウム、カリ物ガラス等が挙げられる。その他の成
分に関しては、Li酸化物、酸化鉄、チタン酸バリウ
ム、チタニウム、ルチル、珪酸ジルコン及びジルコニア
等を用いてもよい。
Also, a plurality of raw materials corresponding to each component may be used. For example, as a SiO 2 source, silica, kaolin, feldspar, mica, talc, mullite, etc., as an Al 2 O 3 source, alumina, kaolin, mullite, bauxite, etc.
Cordierite, magnesium oxide,
Examples of Na 2 O sources such as talc include soda feldspar, sodium oxide, and water glass, and examples of K 2 O sources include potassium feldspar, calcium titanate, and potassium glass. As for other components, Li oxide, iron oxide, barium titanate, titanium, rutile, zircon silicate, zirconia, or the like may be used.

【0027】このような原料から、既知の製造方法によ
りセラミック母材を製造する。例えばシリカを60〜8
0メッシュに粉砕し、ソーダ長石、カリ長石、アルミナ
を所定の比率で配合し325メッシュ以下へ粉砕し、両
者を混合する。
From such raw materials, a ceramic base material is manufactured by a known manufacturing method. For example, if silica is 60-8
The mixture is pulverized to 0 mesh, soda feldspar, potassium feldspar, and alumina are mixed at a predetermined ratio, pulverized to 325 mesh or less, and both are mixed.

【0028】その後、例えば、この原料粉末に、ポリビ
ニルアルコール(PVA205)、ステアリン酸、パラ
フィンワックス、ナフタリンやおがくず等の添加物を加
え、オーブンにより90〜110℃で8〜24時間乾燥
し、40トンの機械圧力により一個当り成形圧力10〜
30kgf/cm2 で所定形態により圧搾成形した後、再度オ
ーブンにより90〜110℃で24時間乾燥し、1,1
80〜1,350℃で6〜14時間塑性する。なお、水
分量は、気孔率の調節により所望の範囲に調節しうる。
また、水分含量の測定は、KSL5502試験方法に準
じて行い、乾燥機で110℃に加熱し2時間後に測定す
る〔水分量=(当初重量−乾燥重量)/乾燥重量×10
0%〕。その後に包装する。
Thereafter, for example, additives such as polyvinyl alcohol (PVA205), stearic acid, paraffin wax, naphthalene, and sawdust are added to the raw material powder, and the mixture is dried in an oven at 90 to 110 ° C. for 8 to 24 hours. The molding pressure per piece is 10
After compression molding in a predetermined form at 30 kgf / cm 2 , it was dried again in an oven at 90 to 110 ° C. for 24 hours.
Plasticize at 80-1,350 ° C for 6-14 hours. The amount of water can be adjusted to a desired range by adjusting the porosity.
The moisture content is measured according to the KSL5502 test method, and is measured after heating at 110 ° C. in a dryer for 2 hours [moisture content = (initial weight−dry weight) / dry weight × 10
0%]. Then package.

【0029】次に、本発明に係るガラス繊維体の製造方
法を説明する。SiO2 :40〜70%、Al23
5〜20%、B23 :3〜15%、CaO:8〜28
%にNa2 O、K2 O、Li2 O等のようなもう一つア
ルカリ金属酸化物1種以上を0.5〜4%重量%を含み
ながら編織されたガラス繊維シートを1重〜10重に重
ねて0.3〜1.5mmの厚さとし、水分含量が0.01
〜0.5%としてガラス繊維積層板を製造する。なお、
水分量は、気孔率の調節により所望の範囲に調節しう
る。
Next, a method for producing a glass fiber body according to the present invention will be described. SiO 2: 40~70%, Al 2 O 3:
5~20%, B 2 O 3: 3~15%, CaO: 8~28
% In Na 2 O, K 2 O, another alkali metal oxide of one or more of the glass fiber sheets knitting or weaving while containing 0.5 to 4% by weight% singlet 10 as Li 2 O, etc. 0.3 to 1.5 mm thick with a water content of 0.01
Manufacture glass fiber laminates with ~ 0.5%. In addition,
The amount of water can be adjusted to a desired range by adjusting the porosity.

【0030】ここで上記のSiO2 、Al23 、B2
3 、CaOとNa2 O、K2 O、Li2 O中1種以上
の純粋原料となったガラス繊維のかわりに上記の組成成
分の各々を含有している鉱物質を混合使用して、本発明
ガラスを製造することができる。
Here, the above SiO 2 , Al 2 O 3 , B 2
O 3 , CaO and Na 2 O, K 2 O, Li 2 O are mixed and used in place of one or more pure glass fibers in place of minerals containing each of the above components, The glass of the present invention can be manufactured.

【0031】原料としては例えば、SiO2 、Al2
3 源としては前記のセラミック母材で挙げたものがあ
り、B23 源として硼砂や硼酸等が挙げられ、CaO
源としては石灰石、白雲石、消石灰、蛍石、珪石灰等が
挙げられる。
As raw materials, for example, SiO 2 , Al 2 O
Examples of the three sources include those described above for the ceramic base material, and examples of the B 2 O 3 source include borax and boric acid.
Sources include limestone, dolomite, slaked lime, fluorite, silica lime and the like.

【0032】このような原料を用いて、既知の製造方法
によりガラス繊維体を製造する。以上のように製造され
た上記のセラミック母材(1)を通常のアルミニウムテ
ープ(2)上に密着させ、上記のガラス繊維積層板
(3)を上記のセラミック母材(1)の上面に密着さ
せ、本発明の自動溶接支持具を有する。
Using such a raw material, a glass fiber body is manufactured by a known manufacturing method. The above-described ceramic base material (1) manufactured as described above is adhered to a normal aluminum tape (2), and the glass fiber laminate (3) is adhered to the upper surface of the ceramic base material (1). And has the automatic welding support of the present invention.

【0033】上記にしたがい、製造されたセラミック母
材の上面に、上記にしたがい製造されたガラス繊維体を
密着させ、更にアルミニウムテープをセラミック母材に
密着させる。このようにして、図1に示すような本発明
の自動溶接用支持具が得られる。
According to the above, the glass fiber body manufactured according to the above is adhered to the upper surface of the manufactured ceramic base material, and further, the aluminum tape is closely adhered to the ceramic base material. Thus, the support for automatic welding of the present invention as shown in FIG. 1 is obtained.

【0034】本発明の自動溶接用支持具において、セラ
ミック母材は溶融金属を保護し、一定の幅と深さ等を有
するバックビードを形成する役割をし、ガラス繊維は鋼
材にセラミック母材が完全に密着するような緩衝材とし
て働き、溶接時に発生するガスを容易に放出し、アンダ
ーカット、スパッタリング、オーバーラップ等とような
溶接欠陥を防止して、良好なバックビード及び形状を有
するよう補助する役割をする。
In the support for automatic welding according to the present invention, the ceramic base material serves to protect the molten metal and form a back bead having a fixed width and depth, and the glass fiber is made of a steel material made of a ceramic base material. Acts as a cushioning material for perfect adhesion, easily releases gas generated at the time of welding, prevents welding defects such as undercut, sputtering, overlap, etc., and helps to have a good back bead and shape Play a role.

【0035】[0035]

【実施例】表1及び表3に示すように、本発明に係る自
動溶接用支持具のセラミック母材とガラス繊維体の組成
成分を変えて各種試験を行った。図1に示すように、通
常の鋼に支持具を取り付ける役割をし、かつ溶接時に発
生するガスを放出するテークホールを多数有するアルミ
ニウムテープ(2)をセラミック母材(1)の低面に取
り付け、またセラミック母材(1)の上部面にはガラス
繊維体(3)を取り付け、下記の溶接条件の下で各種試
験を行い、その結果を表2及び表4に示した。
EXAMPLES As shown in Tables 1 and 3, various tests were conducted by changing the composition of the ceramic base material and the glass fiber body of the support for automatic welding according to the present invention. As shown in FIG. 1, an aluminum tape (2) serving to attach a support to ordinary steel and having a large number of take holes for releasing gas generated during welding is attached to the lower surface of the ceramic base material (1). A glass fiber body (3) was attached to the upper surface of the ceramic base material (1), and various tests were conducted under the following welding conditions. The results are shown in Tables 2 and 4.

【0036】[0036]

【表1】 [Table 1]

【0037】[0037]

【表2】 [Table 2]

【0038】[0038]

【表3】 [Table 3]

【0039】[0039]

【表4】 [Table 4]

【0040】溶接条件: (1)溶接ワイヤ及びフラックス ・L−8*S−707 ・US−40*MF−100N ・Y−B*YB−150 (2)溶接電圧(V): 33 (3)溶接電流(A):900 (4)鋼厚さ : 16mm (5)鋼線突出長さ : 15mm (6)適正ギャップ :2〜3mm (7)溶接姿勢 :下向き姿勢Welding conditions: (1) Welding wire and flux L-8 * S-707 US-40 * MF-100N YB * YB-150 (2) Welding voltage (V): 33 (3) Welding current (A): 900 (4) Steel thickness: 16 mm (5) Steel wire protrusion length: 15 mm (6) Proper gap: 2-3 mm (7) Welding posture: Downward posture

【0041】表2の試験結果によれば、セラミック母材
が本発明の範囲内に属する例4〜9では、溶接ビード外
観とスラグ剥離性及びその他溶接欠陥が全く発生してい
ない溶接ビードを有することが判明した。
According to the test results shown in Table 2, in Examples 4 to 9 in which the ceramic base material falls within the scope of the present invention, the weld bead has a weld bead appearance, slag releasability, and no weld defect at all. It has been found.

【0042】その反面、本発明の範囲外である例1〜3
及び例10は多くの欠陥を有するものである。例1〜3
については、Al23 、MgO量が多く、相対的にS
iO2 量が少ないため、セラミック母材の耐火度が必要
以上高くなり溶融金属の粘性が低下した。したがって、
溶接後スラグ巻かれ現象やビード外観のくぼみ形状等の
溶接上の欠陥を招き、また気孔率が低くセラミック母材
の耐熱衝撃性が低下したため、溶接後セラミック母材が
容易に破損した。また、例10については、溶接ビード
形状及び外観は比較的良好であったが、SiO2 添加量
が過剰であるためセラミック母材の機械的強度が著しく
低下し、セラミック母材の一部が熱衝撃及び外圧に対し
て容易に破損し、溶接後粉塵が発生した。また、水分含
量が高すぎ、溶接時に水分がビード内に微細気孔として
存在し溶接欠陥を招いた。
On the other hand, Examples 1 to 3 which are outside the scope of the present invention
And Example 10 has many defects. Examples 1-3
With respect to the amount of Al 2 O 3 and MgO,
Since the amount of iO 2 was small, the fire resistance of the ceramic base material was increased more than necessary, and the viscosity of the molten metal was reduced. Therefore,
After welding, defects in welding such as slag winding phenomenon and bead appearance hollow shape were caused, and the ceramic base material was easily damaged after welding because the porosity was low and the thermal shock resistance of the ceramic base material was reduced. In Example 10, although the weld bead shape and appearance were relatively good, the mechanical strength of the ceramic base material was significantly reduced due to the excessive amount of SiO 2 added, and a portion of the ceramic base material was thermally degraded. It was easily damaged by impact and external pressure, and dust was generated after welding. In addition, the water content was too high, and water was present as fine pores in the bead during welding, causing welding defects.

【0043】また、表4の試験結果によれば、ガラス繊
維体が本発明の範囲に属する例14〜18では、自動溶
接用支持具として良好の溶接ビードを有することが判明
した。その反面、本発明の範囲外である例11〜13及
び例19〜22では、多くの溶接欠陥が発生した。例1
1〜13については、SiO2 量が少なく、Al23
及びB23 量が多いため、ガラス繊維体の機械的強度
である曲がり強度が低下し、著しい高耐熱性を示した。
そのため、ガラス繊維が細砕し、バックビード形状が必
要以上に広く深く形成され、また、ガラス繊維体の耐熱
性向上によるスラグの粘性の低下によりスラグの巻かれ
現象やオーバーラップ等の溶接欠陥が生じた。また、例
19では、SiO2 量が多く、Al23 及びB23
量が少ないのでガラス繊維体の耐熱性が低下し、そのた
めスラグが過剰発生し、ガス放出が困難になり、フロー
ホール、スパッタリング、スラグの剥離低下等の溶接欠
陥が生じた。また例20では、ガラス繊維体の厚さが薄
すぎて溶接時に発生するガス放出が困難になり、くぼみ
やスラグの剥離性低下等の溶接欠陥を招き、例21及び
例22では、ガラス繊維厚さが必要以上厚すぎてバック
ビードの広さや深さ等を調節するのが困難であり、溶接
時にガラス繊維体がセラミック母材上に残存し、オーバ
ーラップ、スラグの巻かれ現象、フローホール等のよう
な溶接欠陥を招いた。
Further, according to the test results in Table 4, it was found that in Examples 14 to 18 in which the glass fiber body falls within the scope of the present invention, the glass fiber body had a good welding bead as a support for automatic welding. On the other hand, in Examples 11 to 13 and Examples 19 to 22, which are outside the scope of the present invention, many welding defects occurred. Example 1
For, SiO 2 amount is less 1~13, Al 2 O 3
Also, since the amount of B 2 O 3 was large, the bending strength, which was the mechanical strength of the glass fiber body, was reduced, and remarkable high heat resistance was exhibited.
Therefore, the glass fiber is crushed, the back bead shape is formed wider and deeper than necessary, and welding defects such as slag winding phenomenon and overlap due to lowering of slag viscosity due to improvement in heat resistance of the glass fiber body are caused. occured. In Example 19, the amount of SiO 2 was large, and Al 2 O 3 and B 2 O 3
Since the amount was small, the heat resistance of the glass fiber body was reduced, and therefore, slag was excessively generated, gas was difficult to be released, and welding defects such as flow holes, sputtering, and reduced peeling of the slag occurred. Further, in Example 20, the thickness of the glass fiber body was too thin to make it difficult to release gas generated at the time of welding, leading to welding defects such as depressions and reduced slag peelability. In Examples 21 and 22, the glass fiber thickness was reduced. It is difficult to adjust the width and depth of the back bead because it is too thick, and the glass fiber body remains on the ceramic base material during welding, causing overlap, slag winding, flow holes, etc. Such as welding defects.

【図面の簡単な説明】[Brief description of the drawings]

【図1】本発明に係る自動溶接用支持具である。FIG. 1 is a support for automatic welding according to the present invention.

【図2】従来の自動溶接用支持具である。FIG. 2 is a conventional support for automatic welding.

【符号の説明】[Explanation of symbols]

1 セラミック母材 2 アルミニウムテープ 2a マグネチッククランプ 3 ガラス繊維体 4 鋼材 DESCRIPTION OF SYMBOLS 1 Ceramic base material 2 Aluminum tape 2a Magnetic clamp 3 Glass fiber body 4 Steel material

───────────────────────────────────────────────────── フロントページの続き (58)調査した分野(Int.Cl.6,DB名) B23K 37/06 C04B 35/00──────────────────────────────────────────────────続 き Continued on front page (58) Field surveyed (Int.Cl. 6 , DB name) B23K 37/06 C04B 35/00

Claims (2)

(57)【特許請求の範囲】(57) [Claims] 【請求項1】 70〜95重量%のSiO2 、2〜15
重量%のAl23、1〜5重量%のMgO、1.2〜
8重量%のNa2 O及び/またはK2 O並びに0.01
〜0.5重量%の水分を含む、気孔率25〜48%及び
耐火度1,435〜1,670℃のセラミック母材、並
びに該母材上に積層された40〜70重量%のSiO
2 、5〜20重量%のAl23 、3〜15重量%のB2
3 、8〜28重量%のCaO、0.5〜4重量%の
アルカリ金属酸化物及び0.01〜0.5重量%の水分
を含む、厚さ0.3〜1.5mmのガラス繊維体を含むこ
とを特徴とする自動溶接用支持具。
1. A composition comprising 70 to 95% by weight of SiO 2 , 2 to 15% by weight.
Wt% of Al 2 0 3, 1~5 wt% of MgO, 1 .2 to
8% by weight of Na 2 O and / or K 2 O and 0.01
Ceramic matrix having a porosity of 25 to 48% and a fire resistance of 1,435 to 1,670 ° C., containing water of 0.5 to 0.5% by weight, and 40 to 70% by weight of SiO laminated on the matrix.
2, 5 to 20 wt% of Al 2 O 3, 3 to 15 wt% of B 2
O 3, 8 to 28 wt% of CaO, including 0.5-4% by weight of alkali metal oxide and 0.01 to 0.5% by weight of water, glass fibers having a thickness of 0.3~1.5mm A support for automatic welding comprising a body.
【請求項2】 該母材が、石英、トリジマイト及び/ま
たはクリストバライトを含有する、請求項1記載の自動
溶接用支持具。
2. The automatic welding support according to claim 1, wherein the base material contains quartz, tridymite and / or cristobalite.
JP9041974A 1996-02-27 1997-02-26 Automatic welding support Expired - Lifetime JP2857116B2 (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
KR1019960004813A KR0163265B1 (en) 1996-02-27 1996-02-27 Supporter for auto-welding
KR4813/1996 1996-02-27

Publications (2)

Publication Number Publication Date
JPH1024395A JPH1024395A (en) 1998-01-27
JP2857116B2 true JP2857116B2 (en) 1999-02-10

Family

ID=19451879

Family Applications (1)

Application Number Title Priority Date Filing Date
JP9041974A Expired - Lifetime JP2857116B2 (en) 1996-02-27 1997-02-26 Automatic welding support

Country Status (2)

Country Link
JP (1) JP2857116B2 (en)
KR (1) KR0163265B1 (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN100424036C (en) * 2004-04-16 2008-10-08 郑武秀 Ceramic substrate material and welding support rack using said material

Families Citing this family (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
KR100492144B1 (en) * 1997-07-25 2005-08-31 삼성중공업 주식회사 Ceramic backing material for bar joint CO2 welding and butt joint CO2 welding method using the same
KR100966402B1 (en) * 2007-08-28 2010-06-28 대우조선해양 주식회사 Displacement minimum welding method of PCTC main plate welding
JP2011194449A (en) * 2010-03-23 2011-10-06 Sumitomo Metal Pipeline & Piping Ltd Mag welding method
KR102337795B1 (en) * 2015-07-01 2021-12-08 대우조선해양 주식회사 Welding structure for thin plate

Family Cites Families (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5140989B2 (en) * 1971-08-12 1976-11-06
JPS57154399A (en) * 1981-03-20 1982-09-24 Kobe Steel Ltd Backing strip for one-side welding
JPS62244597A (en) * 1986-04-16 1987-10-24 Kobe Steel Ltd Backing strip for welding
JPS643593U (en) * 1987-06-27 1989-01-10
JP2968166B2 (en) * 1994-03-02 1999-10-25 品川白煉瓦株式会社 Method of manufacturing silica brick

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN100424036C (en) * 2004-04-16 2008-10-08 郑武秀 Ceramic substrate material and welding support rack using said material

Also Published As

Publication number Publication date
KR0163265B1 (en) 1999-01-15
KR970061433A (en) 1997-09-12
JPH1024395A (en) 1998-01-27

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