JPH0240433B2 - - Google Patents
Info
- Publication number
- JPH0240433B2 JPH0240433B2 JP60290028A JP29002885A JPH0240433B2 JP H0240433 B2 JPH0240433 B2 JP H0240433B2 JP 60290028 A JP60290028 A JP 60290028A JP 29002885 A JP29002885 A JP 29002885A JP H0240433 B2 JPH0240433 B2 JP H0240433B2
- Authority
- JP
- Japan
- Prior art keywords
- flux
- protective film
- water glass
- intermetallic compound
- corrosion resistance
- 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
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- Nonmetallic Welding Materials (AREA)
Description
[産業上の利用分野]
本発明は、被覆アーク溶接棒、SAW用焼結型
フラツクス、フラツクス入りワイヤ、被覆消耗ノ
ズル等に適用される溶接用フラツクス原料の1つ
として使用される金属間化合物に関し、特に水ガ
ラス耐食性の優れた金属間化合物に関するもので
ある。
[従来の技術]
上述の溶接用フラツクスは、アーク安定剤やス
ラグ生成剤等種々のフラツクス原料を配合し、こ
れに水ガラス等の固着剤を加え、必要により造
粒・焼結して製造されている。そしてこの様な溶
接用フラツクス中に脱酸成分あるいは合金元素添
加成分等としてフエロアロイ(Fe−Si、Fe−Al、
Fe−Ti等)やCa−Si、REM−Ca−Si、Al−Mg
等の金属間化合物が使用されている。
ところで上記金属間化合物と水ガラスを混合す
ると両者が反応してH2が発生し、このH2によつ
て混練フラツクスの内部が空疎なものとなりフラ
ツクスの固着強度低下を招く原因となつているこ
とが指摘されており、次の様な問題が発生してい
る。即ち被覆アーク溶接棒や被覆消耗ノズルにお
いてはフラツクスの耐脱落性能が悪化し製品の歩
留りが低下する。又SAWフラツクスにおいては
フラツクスの粉化率が高くなつて、繰返し使用で
きる回数が減少し製品々質の悪化を招く。更にフ
ラツクス入りワイヤにおいては造粒フラツクスの
粉化によりフラツクス充填時のシントロン性に不
均一を生じシース内のフラツクス成分の偏析が発
生し、ひいては溶接作業性の悪化やビード品質の
悪化等を招く。
そこでこうした問題を解決する為にフラツク原
料である金属間化合物を焙焼して表面に酸化皮膜
を形成したり、化学的処理(乾式あるいは湿式)
により表面に保護皮膜を形成する等の対策が講じ
られており、該表面皮膜によつて金属間化合物素
地と水ガラスとの反応を防止している。
[発明が解決しようとする問題点]
しかるに焙焼及び化学的処理による保護皮膜
は、金属間化合物表面に不均一に形成されること
が多く、十分な保護機能を付与する為には処理時
間を長くしたり、多量の薬品を使用しなければな
らない等の不都合がある。又この様にして形成さ
れた保護皮膜は下地である金属間化合物素地との
密着性が必ずしも良好ではなく、フラツクス原料
の混練操作中にフラツクス原料同士の摩擦によつ
て保護皮膜が剥離し、保護皮膜としての機能を果
たさなくなる。即ち保護皮膜が剥離すると素地が
露出して化学的な活性度が増大するので水ガラス
や水との反応が起こりH2が生成する。その結果
生成H2により混合フラツクスが膨張し、フラツ
クス粒子同士の接触面積が低下して乾燥後におけ
るフラツクス固着強度の低下に至るものと考えら
れる。
本発明はこうした事情に着目してなされたもの
であつて、上記保護皮膜の分布不均一性及び易剥
離性等の欠点が解消され、水ガラスに対する耐食
性が良好である様なフラツクス原料としての金属
間化合物を提供しようとするものである。
[問題点を解決するための手段]
しかして上記目的を達成した本発明の金属間化
合物とは、Bを0.1〜8%(重量%の意味、以下
同じ)含有する点に要旨を有するものである。
[作用]
焙焼や化学的処理等の後処理によつて金属間化
合物表面に形成した保護皮膜では処理条件を種々
変更しても前述の欠点を抜本的に解消するに至ら
ない。そこで本発明者等は、金属間化合物表面に
均一で且つ素地との密着性の高い保護皮膜を形成
するには上述のような強制的手段によるのではな
く、金属Al表面のAl2O3皮膜の如く自然に生成し
たものでなければならないのではないかと考え
た。即ち自然生成保護皮膜であればその生成態様
は金属間化合物表面全体に均一且つ緻密に生成
し、素地との密着性も高いのではないかとの考察
をなすに至り種々研究を重ねた結果前記構成に到
達した。
即ち本発明のBを含有する金属間化合物はBの
易酸化性に基づき、その表面にB酸化物の皮膜を
自然に生成する。その結果酸化皮膜の形成態様は
分布が均一で且つ緻密でありしかも素地との密着
性も強固である。こうして金属間化合物表面は安
定で且つ均質なB酸化物皮膜で覆われ、不活性と
なるので、水ガラスと接触してもこれによつて腐
食されることがなく、その耐食性能はフラツクス
の混合時等の摩擦程度では容易に低下することが
ない。
上記作用効果を有効に発揮させる為には金属間
化合物中にBを0.1〜8%含有させる必要があり、
B量が0.1%未満の場合にはB添加量が不足する
為に保護皮膜厚さが不十分であり、水ガラス耐食
性の良好な金属間化合物が得られない。一方B量
が8%を超えると金属間化合物表面に形成される
保護皮膜が厚くなりすぎ、その為に保護皮膜と下
地との密着性が悪化してフラツクス原料混合時の
摩擦・衝突により剥離することが多くなる。即ち
水ガラス耐食性が悪化する。
本発明の基本構成は上記の通りであるが、本発
明に係る金属間化合物は高温における耐熱性(耐
高温酸化性)が良く、高温雰囲気中で酸化皮膜厚
さが不必要に増大することがない他、例えば非造
粒フラツクスを充填したフラツクス入りワイヤに
おいてはワイヤ外皮を焼鈍した際の金属間化合物
の酸化が少ないといつた特長をも有している。従
つて本発明に係る金属間化合物は水ガラスを使用
しない溶接用フラツクスに対しても有用である。
尚上記の様な本発明に係るB含有金属間化合物
を製造するに当たつては、Fe−Si、Fe−Mn、
Ca−Si等を溶製する際に金属B若しくはB化合
物(酸化物、炭化物、窒化物等)を原料として添
加すればよい。溶製後の処理は、常法即ち造塊→
粉砕→篩分けの処理に従えばよい。
[実施例]
実施例 1
第2表に示す各B濃度のFe−Siを用い、第1
表に示すフラツクス組成の被覆アーク溶接棒を常
法に従つて製造した。但し、用いた心線は、4mm
φ×400ml、フラツクスの乾燥条件は、400℃×30
分とした。又、水ガラスの添加量は原料フラツク
ス100g当たり14mlとした。
この実験において、被覆剤の乾燥割れ状況を比
較すると共に、乾燥割れのない製品の歩留り、耐
脱落性能を調べたところ第2表に示す結果が得ら
れた。
[Field of Industrial Application] The present invention relates to an intermetallic compound used as one of the welding flux raw materials applied to coated arc welding rods, sintered fluxes for SAW, flux-cored wires, coated consumable nozzles, etc. In particular, it relates to intermetallic compounds with excellent water glass corrosion resistance. [Prior Art] The above-mentioned welding flux is manufactured by blending various flux raw materials such as arc stabilizers and slag forming agents, adding a fixing agent such as water glass, and granulating and sintering as necessary. ing. Ferroalloys (Fe-Si, Fe-Al, Fe-Si, Fe-Al,
Fe-Ti, etc.), Ca-Si, REM-Ca-Si, Al-Mg
Intermetallic compounds such as are used. By the way, when the above-mentioned intermetallic compound and water glass are mixed, the two react to generate H 2 , and this H 2 makes the inside of the kneaded flux void and causes a decrease in the fixing strength of the flux. It has been pointed out that the following problems have occurred. That is, in coated arc welding rods and coated consumable nozzles, the flux drop-off resistance deteriorates, resulting in a decrease in product yield. Furthermore, in the case of SAW flux, the pulverization rate of the flux increases, reducing the number of times it can be used repeatedly, leading to deterioration of product quality. Furthermore, in flux-cored wires, the pulverization of granulated flux causes non-uniform syntron properties during flux filling, causing segregation of flux components within the sheath, which in turn leads to deterioration of welding workability and deterioration of bead quality. Therefore, in order to solve these problems, the intermetallic compounds that are raw materials for the flakes are roasted to form an oxide film on the surface, and chemical treatments (dry or wet) are used.
Measures have been taken to form a protective film on the surface, and this surface film prevents the reaction between the intermetallic compound base and water glass. [Problems to be solved by the invention] However, the protective film formed by roasting and chemical treatment is often formed unevenly on the surface of the intermetallic compound, and in order to provide a sufficient protective function, it is necessary to take a long treatment time. There are inconveniences such as having to take a long time and using a large amount of chemicals. In addition, the protective film formed in this way does not necessarily have good adhesion to the underlying intermetallic compound base, and the protective film peels off due to friction between the flux raw materials during the kneading operation of the flux raw materials. It no longer functions as a film. That is, when the protective film peels off, the base material is exposed and its chemical activity increases, causing a reaction with water glass and water to generate H 2 . As a result, the mixed flux expands due to the generated H2 , and the contact area between the flux particles decreases, which is thought to lead to a decrease in the fixation strength of the flux after drying. The present invention has been made in view of these circumstances, and provides a metal as a raw material for a flux that eliminates the disadvantages such as non-uniform distribution and easy peelability of the protective film and has good corrosion resistance against water glass. The aim is to provide intermediate compounds. [Means for Solving the Problems] The intermetallic compound of the present invention that achieves the above object is characterized by containing 0.1 to 8% B (meaning % by weight, the same applies hereinafter). be. [Function] In the case of a protective film formed on the surface of an intermetallic compound by post-treatment such as roasting or chemical treatment, the above-mentioned drawbacks cannot be completely eliminated even if the treatment conditions are variously changed. Therefore, in order to form a uniform protective film on the surface of the intermetallic compound and with high adhesion to the substrate, the present inventors decided to use an Al 2 O 3 film on the surface of the metal Al, instead of using the above-mentioned forced means. I thought that it must be something that was naturally generated, like this. In other words, after conducting various studies, we came to the conclusion that a naturally occurring protective film would form uniformly and densely over the entire surface of the intermetallic compound, and would have a high degree of adhesion to the substrate. reached. That is, the B-containing intermetallic compound of the present invention naturally forms a B oxide film on its surface based on the oxidizability of B. As a result, the oxide film is formed in a manner that the distribution is uniform and dense, and the adhesion to the substrate is strong. In this way, the surface of the intermetallic compound is covered with a stable and homogeneous B oxide film and becomes inert, so it will not be corroded even when it comes into contact with water glass, and its corrosion resistance is improved by the flux mixture. It does not easily decrease due to friction due to time, etc. In order to effectively exhibit the above effects, it is necessary to contain 0.1 to 8% of B in the intermetallic compound.
If the amount of B is less than 0.1%, the thickness of the protective film will be insufficient because the amount of B added will be insufficient, and an intermetallic compound with good water glass corrosion resistance will not be obtained. On the other hand, if the amount of B exceeds 8%, the protective film formed on the surface of the intermetallic compound becomes too thick, which deteriorates the adhesion between the protective film and the substrate and causes it to peel off due to friction and collision when mixing the flux raw materials. It happens a lot. That is, water glass corrosion resistance deteriorates. The basic structure of the present invention is as described above, but the intermetallic compound according to the present invention has good heat resistance at high temperatures (high temperature oxidation resistance), and the oxide film thickness does not increase unnecessarily in a high temperature atmosphere. In addition, for example, a flux-cored wire filled with non-granulated flux has the advantage that intermetallic compounds are less likely to be oxidized when the wire sheath is annealed. Therefore, the intermetallic compound according to the present invention is also useful for welding fluxes that do not use water glass. In addition, in producing the B-containing intermetallic compound according to the present invention as described above, Fe-Si, Fe-Mn,
Metal B or a B compound (oxide, carbide, nitride, etc.) may be added as a raw material when melting Ca-Si or the like. Processing after melting is the usual method, that is, ingot formation →
Just follow the process of crushing → sieving. [Example] Example 1 Using Fe-Si with each B concentration shown in Table 2, the first
Coated arc welding rods having the flux composition shown in the table were manufactured according to a conventional method. However, the core wire used is 4mm.
φ×400ml, flux drying conditions are 400℃×30
It was a minute. The amount of water glass added was 14 ml per 100 g of raw material flux. In this experiment, the dry cracking conditions of the coating materials were compared, and the yield and shedding resistance of products without dry cracking were investigated, and the results shown in Table 2 were obtained.
【表】【table】
【表】【table】
【表】【table】
【表】
第2表に示す様にNo.1、2はB濃度が低い為、
Fe−Si表面に保護皮膜が十分に形成されずFe−
Siの水ガラス耐食度が十分でない例であり、製品
歩留、耐脱落性能共に不良であつた。No.9、10
は、B濃度が高すぎる為、保護皮膜が厚く生成
し、保護皮膜と、下地との密着性が悪くなり、フ
ラツクス粒子同士の摩擦衝突により保護皮膜の剥
離が起こり、Fe−Siの水ガラス耐食度は却つて
悪くなつた。又実験No.9、10の製品歩留及び耐脱
落性能は共に不良であつた。
これらに反し本発明例であるNo.3〜8は、製品
歩留、耐脱落性能がいずれも良好であつた。
実施例 2
第4表に示す各B濃度のFe−Mnを用い第3表
に示すフラツクス組成の被覆アーク溶接棒を、実
施例1と同様にして製造した。
この実験において被覆剤の乾燥割れ状況を比較
すると共に、乾燥割れのない製品の歩留、耐脱落
性能を調べたところ第4表に示す結果が得られ
た。[Table] As shown in Table 2, No. 1 and 2 have low B concentration, so
A protective film is not sufficiently formed on the Fe−Si surface and Fe−
This is an example of Si having insufficient water glass corrosion resistance, and both product yield and drop-off resistance were poor. No.9, 10
Because the B concentration is too high, the protective film is formed thickly, the adhesion between the protective film and the substrate becomes poor, and the protective film peels off due to frictional collisions between flux particles, resulting in water glass corrosion resistance of Fe-Si. My condition actually got worse. Moreover, both the product yield and the falling-off resistance performance of Experiment Nos. 9 and 10 were poor. On the contrary, Nos. 3 to 8, which are examples of the present invention, had good product yield and anti-dropping performance. Example 2 Coated arc welding rods having the flux compositions shown in Table 3 were manufactured in the same manner as in Example 1 using Fe-Mn of each B concentration shown in Table 4. In this experiment, the drying cracking of the coating materials was compared, and the yield and shedding resistance of products without drying cracking were investigated, and the results shown in Table 4 were obtained.
【表】【table】
【表】【table】
【表】【table】
【表】
*1、*2、*3 第2表に同じ
第4表に示す様に、No.1、2は、B濃度が低い
為、フエロマンガン表面に保護皮膜が十分に形成
されず、フエロマンガンの耐食性が十分でない例
であり、製品歩留、耐脱落性能共に不良であつ
た。No.8は、B濃度が高すぎる例であり、実施例
1の場合と同様、生成した厚い保護皮膜と下地と
の密着性が悪い為、混練に伴うフラツクス粒子同
士の摩擦・衝突により、保護皮膜の剥離が起こ
り、フエロマンガンの耐食性がかえつて悪くなつ
た。又No.8の製品歩留、耐脱落性能は不良であつ
た。
これらに反し、No.3〜7は全て本発明条件を満
足しており、良好な製品歩留、耐脱落性能が得ら
れた。
実施例 3
第6表に示す各B濃度のAl−Mgを用い、第5
表に示すフラツクス組成のフラツクス入りワイヤ
用充填フラツクスを常法に従つて造粒し製造し
た。
水ガラス添加量は、原料フラツクス100g当た
り13ml、造粒フラツクスの乾燥条件は、350℃×
1時間、粒度は20×65メツシユとした。
この実験において、粒度調整されたフラツクス
がシースに充填される迄に粉化される割合、即ち
粉化率を調査したところ第6表に示す結果が得ら
れた。粉化率が高いもの程、シントロン性が悪
く、フラツクスの偏析が生じやすい。[Table] *1, *2, *3 Same as Table 2 As shown in Table 4, Nos. 1 and 2 have a low B concentration, so a protective film is not sufficiently formed on the ferromanganese surface, and the ferromanganese This is an example of insufficient corrosion resistance, and both product yield and drop-off resistance were poor. No. 8 is an example in which the B concentration is too high, and as in the case of Example 1, the adhesion between the thick protective film formed and the base is poor, so the friction and collision between flux particles during kneading prevents protection. The film peeled off, and the corrosion resistance of ferromanganese worsened. Moreover, the product yield and anti-dropping performance of No. 8 were poor. On the contrary, all Nos. 3 to 7 satisfied the conditions of the present invention, and good product yield and drop-off resistance were obtained. Example 3 Using Al-Mg with each B concentration shown in Table 6,
A filling flux for a flux-cored wire having the flux composition shown in the table was granulated and manufactured according to a conventional method. The amount of water glass added was 13ml per 100g of raw material flux, and the drying conditions for the granulated flux were 350℃
The particle size was 20×65 mesh for 1 hour. In this experiment, the rate at which the particle size-adjusted flux was pulverized before it was filled into the sheath, ie, the pulverization rate, was investigated, and the results shown in Table 6 were obtained. The higher the pulverization rate, the worse the syntron properties and the more likely flux segregation will occur.
【表】【table】
【表】
第6表に示す様にNo.1、2は、B濃度が低い為
Al−Mgの水ガラス耐食性が悪く造粒フラツクス
粒子の粉化率が悪かつた例である。
No.9は、B濃度が高すぎた例であり、形成され
た厚い保護皮膜は、下地との密着性が悪く、その
為フラツクス混練時にフラツクス粒子同士の摩
擦・衝突により、保護皮膜の剥離が起こり、Al
−Mgの耐食性が改善されず、粉化率も悪い結果
が得られた。
これらに反しNo.3〜8は、全て本発明条件を満
足しており、Al−Mgに添加されたBにより、Al
−Mgの水ガラス耐食性が改善され、低レベルの
粉化率を示した。
実施例 4
第8表に示す各B濃度のREM Ca−Siを用い、
第7表に示すフラツクス組成の潜弧溶接用焼成型
フラツクスを常法に従つて製造した。
水ガラス添加量は原料フラツクス100g当たり
13ml、造粒フラツクスの焼成条件は450℃×2時
間、製品フラツクスの粒度調整は、12×65メツシ
ユとした。
この実験において、潜弧溶接用フラツクスの造
粒歩留り及び繰返し使用回数を調査したところ、
第8表に示す結果が得られた。[Table] As shown in Table 6, No. 1 and 2 have low B concentration.
This is an example of poor water glass corrosion resistance of Al-Mg and poor pulverization rate of granulated flux particles. No. 9 is an example in which the B concentration was too high, and the thick protective film that was formed had poor adhesion to the base, and as a result, the protective film could be peeled off due to friction and collision between flux particles during flux kneading. Happens, Al
- The corrosion resistance of Mg was not improved and the powdering rate was also poor. On the contrary, Nos. 3 to 8 all satisfied the conditions of the present invention, and B added to Al-Mg caused Al
- The water glass corrosion resistance of Mg was improved and showed a low level of powdering rate. Example 4 Using REM Ca-Si with each B concentration shown in Table 8,
Sintered fluxes for submerged arc welding having the flux composition shown in Table 7 were manufactured according to a conventional method. The amount of water glass added is per 100g of raw material flux.
The firing conditions for the 13 ml granulated flux were 450°C x 2 hours, and the particle size adjustment of the product flux was 12 x 65 mesh. In this experiment, the granulation yield and number of repeated uses of flux for submerged arc welding were investigated.
The results shown in Table 8 were obtained.
【表】【table】
【表】
第8表に示す様にNo.1、2は、B濃度が低い為
にREM Ca−Si表面に保護皮膜が十分に形成さ
れず、REM Ca−Siの水ガラス耐食性が改善さ
れなかつた例であり、製品歩留、繰返し使用回数
共に悪い結果が得られた。
No.9は、B濃度が高すぎた例であり、実施例1
〜3の場合と同様高いB濃度の為に、保護皮膜が
厚くなり、保護皮膜と下地との密着性が悪化し、
混練→造粒に伴うフラツクス粒子同士の摩擦・衝
突により保護皮膜が剥離し、REM Ca−Siの水
ガラス耐食性がかえつて悪くなり、造粒歩留、繰
返し使用回数は共にやはり悪い結果が得られた。
これらに反しNo.3〜8は全て本発明条件を満た
しており、造粒歩留、繰返し使用回数共良好な結
果が得られた。
[発明の効果]
本発明は以上の様に構成されており、水ガラス
耐食性の優れたフラツクス原料用金属間化合物を
提供することができ、この結果固着強度の優れた
各種溶接用フラツクスを提供することができる様
になつた。[Table] As shown in Table 8, in Nos. 1 and 2, due to the low B concentration, a protective film was not sufficiently formed on the REM Ca-Si surface, and the water glass corrosion resistance of REM Ca-Si was not improved. In this example, poor results were obtained in terms of product yield and number of repeated uses. No. 9 is an example in which the B concentration was too high, and Example 1
As in case 3, the protective film becomes thick due to the high B concentration, and the adhesion between the protective film and the base deteriorates.
The protective film peels off due to friction and collision between flux particles during kneading and granulation, and the water glass corrosion resistance of REM Ca-Si worsens, resulting in poor results in terms of granulation yield and number of repeated uses. Ta. On the contrary, Nos. 3 to 8 all satisfied the conditions of the present invention, and good results were obtained in terms of granulation yield and number of repeated uses. [Effects of the Invention] The present invention is configured as described above, and it is possible to provide an intermetallic compound for flux raw materials that has excellent water glass corrosion resistance, and as a result, provides various welding fluxes that have excellent bonding strength. I am now able to do this.
第1図は実施例4の実験における開先形状を示
す模式図である。
FIG. 1 is a schematic diagram showing the groove shape in the experiment of Example 4.
Claims (1)
間化合物であつて、Bを0.1〜8重量%含有する
ことを特徴とする水ガラス耐食性の優れた金属間
化合物。1. An intermetallic compound used as a raw material for welding flux, which is characterized by containing 0.1 to 8% by weight of B and having excellent water glass corrosion resistance.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP29002885A JPS62148099A (en) | 1985-12-23 | 1985-12-23 | Intermetallic compound having excellent corrosion resistance to water glass |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP29002885A JPS62148099A (en) | 1985-12-23 | 1985-12-23 | Intermetallic compound having excellent corrosion resistance to water glass |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS62148099A JPS62148099A (en) | 1987-07-02 |
| JPH0240433B2 true JPH0240433B2 (en) | 1990-09-11 |
Family
ID=17750848
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP29002885A Granted JPS62148099A (en) | 1985-12-23 | 1985-12-23 | Intermetallic compound having excellent corrosion resistance to water glass |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS62148099A (en) |
Families Citing this family (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP4672563B2 (en) * | 2006-02-02 | 2011-04-20 | 日鐵住金溶接工業株式会社 | Iron-based Mn-B alloy powder for flux cored wire |
| JP4680082B2 (en) * | 2006-02-09 | 2011-05-11 | 日鐵住金溶接工業株式会社 | Flux-cored wire for gas shielded arc welding |
Family Cites Families (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS5853393A (en) * | 1981-09-26 | 1983-03-29 | Nippon Steel Corp | Covered arc welding rod generating low hydrogen atmosphere |
| JPS6032559A (en) * | 1983-08-01 | 1985-02-19 | Mitsubishi Mining & Cement Co Ltd | Electric winding and manufacture thereof |
-
1985
- 1985-12-23 JP JP29002885A patent/JPS62148099A/en active Granted
Also Published As
| Publication number | Publication date |
|---|---|
| JPS62148099A (en) | 1987-07-02 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| LAPS | Cancellation because of no payment of annual fees |