JPS59150666A - Anti-spatter agent - Google Patents

Anti-spatter agent

Info

Publication number
JPS59150666A
JPS59150666A JP2573883A JP2573883A JPS59150666A JP S59150666 A JPS59150666 A JP S59150666A JP 2573883 A JP2573883 A JP 2573883A JP 2573883 A JP2573883 A JP 2573883A JP S59150666 A JPS59150666 A JP S59150666A
Authority
JP
Japan
Prior art keywords
zirconium
zirconium oxide
compd
welding
oxide
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
JP2573883A
Other languages
Japanese (ja)
Inventor
Masakazu Tokuoka
徳岡 優和
Kazuo Tsuruoka
鶴岡 和男
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.)
NOF Corp
Original Assignee
NOF Corp
Nippon Oil and Fats Co 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 NOF Corp, Nippon Oil and Fats Co Ltd filed Critical NOF Corp
Priority to JP2573883A priority Critical patent/JPS59150666A/en
Publication of JPS59150666A publication Critical patent/JPS59150666A/en
Pending 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
    • B23K9/00Arc welding or cutting
    • B23K9/32Accessories

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  • Engineering & Computer Science (AREA)
  • Physics & Mathematics (AREA)
  • Plasma & Fusion (AREA)
  • Mechanical Engineering (AREA)
  • Nonmetallic Welding Materials (AREA)

Abstract

PURPOSE:To prevent sticking of spatter during welding at a high temp., multi- layer build-up welding and melt cutting by using an anti-spatter agent contg. zirconium oxide or a zirconium compd. forming zirconium oxide when heated as an effective component. CONSTITUTION:The reason for using zirconium oxide or a zirconium compd. lies in that the zirconium oxide has a high m.p. and does not change physically at the temp. generated in welding and that the zirconium oxide has the same coefft. of thermal expansion as metals and when said zirconium is coated on a steel plate, the coated film thereof is hardly strippable and has good adhesion. The zirconium oxide has small affinity to metals, has weak adhesion power to a molten metal so that the removal thereof is easy. The zirconium compd. stabilizes the arc and permits easy formation of slag. The zirconium compd. is exemplified by zirconium hydroxide, basic zirconium carbonate, zirconium stearate, etc. The zirconium oxide or zirconium compd. is used by using other inorg. pigment according to need in 50-90w% zirconium oxide or zirconium compd., compounding water, a solvent and a synthetic resin therewith and preparing the mixture into a past or paint form.

Description

【発明の詳細な説明】 本発明は、金属材料の溶接または溶断を行うときに発生
する、溶接周辺部のスパッタの付着を防止する耐熱性ス
パッタ付着防止剤に関する。
DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a heat-resistant spatter adhesion inhibitor that prevents adhesion of spatter around the welding area that occurs when welding or fusing metal materials.

船舶、橋梁、建築、その他各種の機械を製造する過程で
、溶接、溶断を行い製造する際に、溶融金属が飛散して
溶接、溶断の周辺部に付着すると、その付着した部分は
錆が発生しやすく、さらにその上に塗料を塗装しても、
錆の発生を防止することができないため取り除く必要が
あるが、付着が強固であるため、ディスクグラインダー
やタガネ等の工具を使用して取り除かなくてはならない
。。
During the manufacturing process of ships, bridges, buildings, and other types of machinery, when welding and cutting are performed, if molten metal scatters and adheres to the area around the welding or cutting, rust will occur in the attached area. It is easy to paint, and even if you apply paint on top of it,
Since rust cannot be prevented from forming, it must be removed, but since the adhesion is strong, tools such as a disc grinder or chisel must be used to remove it. .

この作業はかなりの労力と時間を要するため、予め鋼板
上にスパッタ付着防止剤を塗布1また後、溶接、溶断を
行なうことが通常行われている。
Since this work requires a considerable amount of labor and time, it is common practice to apply a spatter adhesion prevention agent to the steel plate in advance, and then weld and fuse the plate.

従来このようカスバッタ付着防止剤には、一般に酸性白
土や酸化チタン、炭酸カルシウムのような無機顔料と樹
脂溶液の分散物、あるいは樹脂を不燃溶剤または水に溶
解、分散したものが使用されているが、これらは耐熱性
に全く欠ける点があり、耐熱用、多層盛用に適していな
い。
Conventionally, such scum locust adhesion prevention agents have generally used a dispersion of an inorganic pigment such as acid clay, titanium oxide, or calcium carbonate and a resin solution, or a resin dissolved or dispersed in a nonflammable solvent or water. , these have a complete lack of heat resistance and are not suitable for heat resistance or multilayer applications.

耐熱用、多層盛用などとしては、無機顔料として二硫化
モリブデンを用いる方法が特開昭53−6274号公報
として公開されているが、二硫化モリブデンは希ガス中
で450℃になると昇華する性質があり、溶接時の高温
により昇華17た二硫化モリブデンが、金属の融けてい
る溶接部分へ容易に入り込み、溶接部分の硫黄成分を増
加させて脆化原因となる欠点がある。また黒鉛を用いる
特公昭48−30533号公報の方法では、黒鉛が主成
分く10〜90%)の塗膜であるため、溶接熱によって
黒鉛の塗膜が・・り離し、金属が融けている溶接部分に
混入すると、m着金属の炭素量を点がある。
For heat-resistant and multi-layer applications, a method using molybdenum disulfide as an inorganic pigment has been disclosed in JP-A-53-6274, but molybdenum disulfide has the property of sublimating at 450°C in a rare gas. There is a drawback that molybdenum disulfide, which sublimes due to the high temperature during welding, easily enters the welded part where the metal is molten, increasing the sulfur content of the welded part and causing embrittlement. In addition, in the method disclosed in Japanese Patent Publication No. 48-30533 that uses graphite, since the coating film is mainly composed of graphite (10 to 90%), the graphite coating peels off due to welding heat and the metal melts. If mixed into the welded part, the amount of carbon in the deposited metal will be reduced.

本発明者は、上記問題について鋭意研究した結果、無機
顔料としてジルコニウム化合物を用いた場合、効果があ
ることが判明し本発明を完成した。
As a result of intensive research into the above-mentioned problem, the present inventor found that the use of a zirconium compound as an inorganic pigment is effective and completed the present invention.

すなわち本発明は 酸化ジルコニウムまたは加熱によって酸化ジルコニウム
を生成するジルコニウム化合物を有効酸化合物を用いる
理由は、生成した酸化ジルコニウムは融点が2700℃
と高く、溶接周辺部で発生する温度(約800〜150
0℃)では物理的変化を生じないうえ、金属と熱膨張係
数がほとんど同一であり、金属の伸縮と同じに伸縮する
ため、鋼板に塗布され密着した酸化ジルコニウム塗膜は
剥れ難く密着性が良い。また、酸化ジルコニウムは金属
との親和性が小さく、溶融金属との付着力が弱くて除去
が容易であるため、重ねて溶接を行なう多層盛溶接では
溶接作業が容易である。さらに酸化ジルコニウムは、溶
接に際しアークを安定させ、スラグの形成を容易にする
性質があるため、開先面に付着しても溶接作業に支障を
与えず、むしろ好結果を生ずるため溶接時に特別な配慮
を必要としない特徴があるからである。
That is, the reason why the present invention uses zirconium oxide or a zirconium compound that produces zirconium oxide by heating as an effective acid compound is that the produced zirconium oxide has a melting point of 2700°C.
The temperature generated around the welding area is as high as 800~150℃.
At 0°C), there is no physical change, and the coefficient of thermal expansion is almost the same as that of metal, so it expands and contracts in the same way as metal, so the zirconium oxide coating that is applied to the steel plate and adheres to it is difficult to peel off and has good adhesion. good. In addition, zirconium oxide has a low affinity with metals, has a weak adhesion to molten metal, and is easy to remove, so welding work is easy in multilayer welding in which welding is performed in layers. Furthermore, zirconium oxide has the property of stabilizing the arc during welding and facilitating the formation of slag, so even if it adheres to the groove surface, it does not interfere with welding work, and in fact produces good results, so it is necessary to use special materials during welding. This is because it has characteristics that do not require consideration.

酸化ジルコニウム以外に本発明で使用する溶接、溶断時
の加熱で酸化ジルコニウムとなるジルコニウム化合物々
しては、水酸化ジルコニウム、塩基性炭酸ジルコニウム
、ジルコニウムステアレート等であって、例えば水酸化
ジルコニウムは塩基性炭酸ジルコニウムは 500〜600℃ 3ZrO2・CO2@nH2O3zr02ジルコニウム
ステアレートハ のどとく酸化ジルコニウムとなって、前記酸化ジルコニ
ウムの持つ効果を発揮する。
In addition to zirconium oxide, zirconium compounds that become zirconium oxide when heated during welding or fusing include zirconium hydroxide, basic zirconium carbonate, zirconium stearate, etc. For example, zirconium hydroxide is a basic zirconium compound. At 500-600°C, 3ZrO2.CO2@nH2O3zr02 zirconium stearate becomes zirconium oxide and exhibits the effects of the zirconium oxide.

のであって、必要により他の無機顔料を併用し、水や溶
剤、合成樹脂を配合してペースト状または塗料状として
使用される。
It is used in the form of a paste or paint by adding other inorganic pigments and water, a solvent, or a synthetic resin if necessary.

本発明で酸化ジルコニウムまたはジルコニウム化合物と
併用される無機顔料は、炭酸カルシウム、シリカ、酸化
チタン、硅酸カルシウム等であって1〜50%使用され
る。これら炭酸塩、酸化物、硅酸塩はスパッタ付着防止
剤の密着性を助長する効果があり、不用意に溶接部位に
付着しても剥離樹脂は、フェノール変性アルキド樹脂、
アクリル樹脂、エポキシ樹脂、メチルセルローズ、尿素
樹脂、メラミン樹脂、ポリウレタン樹脂等であって1〜
10%使用する。
The inorganic pigment used in combination with zirconium oxide or a zirconium compound in the present invention is calcium carbonate, silica, titanium oxide, calcium silicate, etc., and is used in an amount of 1 to 50%. These carbonates, oxides, and silicates have the effect of promoting the adhesion of the spatter adhesion prevention agent, and even if it accidentally adheres to the welding area, the peeling resin can be removed by phenol-modified alkyd resin,
Acrylic resin, epoxy resin, methyl cellulose, urea resin, melamine resin, polyurethane resin, etc. 1 to
Use 10%.

スパッタ付着防止剤に流動性を与え、ペースト状、塗料
状とするための溶媒としては、水または溶剤を用いるが
、溶剤としては安全性の点から引 5− 人件のない1,1.1 )リクロルエタン、トリクロル
エチレン、テトラクロロ−1,2ジクロロエタン、1゜
1.2トリクロロフロロエタンなどが好ましい。
Water or a solvent is used as a solvent to impart fluidity to the spatter adhesion preventive agent and make it into a paste or paint form, but water or a solvent is not used for safety reasons. Lichloroethane, trichloroethylene, tetrachloro-1,2 dichloroethane, 1°1.2 trichlorofluoroethane and the like are preferred.

またその配合量は上記ペースト状、塗料状となす条件を
満たす範囲で任意に配合する。
Further, the amount thereof to be blended can be arbitrarily determined within a range that satisfies the above-mentioned conditions for forming the paste-like or paint-like composition.

本発明のスパッタ付着防止剤の製法は、合成樹脂を使用
しないペーストの場合、水または溶剤中に顔料が均一に
分散するまで撹拌し、塗料状の場合、水または溶剤の中
へ合成樹脂を加えて溶解した樹脂溶液に顔料を加え、顔
料が均一に分散するまで撹拌し製造する。
The method for producing the spatter adhesion prevention agent of the present invention is to stir the pigment in water or a solvent until it is uniformly dispersed in the case of a paste that does not use a synthetic resin, and to add the synthetic resin to water or a solvent in the case of a paint. The pigment is added to the dissolved resin solution and stirred until the pigment is uniformly dispersed.

かくして得られた本発明のスパッタ付着防止剤は、特殊
鋼々どの予熱を必要とする高温時の溶接、多層盛溶接ま
たは溶断などの特に耐熱性を必要とする用途に対し、充
分な付着防止効果を与えるものである。
The thus obtained spatter adhesion inhibitor of the present invention has a sufficient adhesion prevention effect for applications that require particularly heat resistance, such as welding special steels at high temperatures that require preheating, multilayer welding, and fusing. It gives

以下実施例を挙げてこの発明の効果を具体的に説明する
The effects of the present invention will be specifically explained below with reference to Examples.

実施例1 撹拌機を備えた容量50(1+m!の容器を用い、酸 
6− 化ジルコニウム1502を容器に入れ、次に1,1゜1
トリクロルエタン80fを容器に入れ、撹拌を40分間
行い、1,1.1 )ジクロルエタンと酸化ジルコニウ
ムを混練させる。次に残りの1.1.1 )ジクロルエ
タン46Fを入れて、撹拌を15分間行い、充分懸濁さ
せ、スパッタ付着防止剤を得た。
Example 1 Using a container with a capacity of 50 (1+ m!) equipped with a stirrer, acid
6- Put zirconium 1502 oxide in a container, then 1,1°1
80f of trichloroethane is placed in a container and stirred for 40 minutes to knead 1,1.1) dichloroethane and zirconium oxide. Next, the remaining 1.1.1) dichloroethane 46F was added and stirred for 15 minutes to sufficiently suspend the mixture to obtain a sputter adhesion inhibitor.

実施例2 実施例1と同じ設備を用い、酸化ジルコニウム231g
、炭酸カルシウム(粒径01〜1μm)152を容器に
入れ、次に水1202を加えて、撹拌を40分間行った
後、次にアロロン580(アルキッドエマルジョン、商
品名、日本触媒化学工業■製)15fと防錆剤159を
入れて撹拌を15分間行い充分懸濁させ、スパッタ付着
防止剤を得た。
Example 2 Using the same equipment as Example 1, 231 g of zirconium oxide
, put calcium carbonate (particle size 01-1 μm) 152 into a container, then add water 1202, stir for 40 minutes, and then add Aloron 580 (alkyd emulsion, trade name, manufactured by Nippon Shokubai Chemical Industry Co., Ltd.) 15f and Rust Preventive Agent 159 were added and stirred for 15 minutes to fully suspend the mixture to obtain a spatter adhesion inhibitor.

実施例3 実施例1と同じ設備を用い、水酸化ジルコニウム150
S’、シリカ151Fを容器に入れ、次に水9931を
加えて、撹拌を40分間行い、充分混練を行った後、次
に2号ケイ酸ソーダ(JIS規格品)37と次にアロロ
ン580(前出)257Vを加えて撹拌を15分間行い
、充分懸濁させ、スパッタ付着防止剤を得た。
Example 3 Using the same equipment as in Example 1, zirconium hydroxide 150
S' and silica 151F were placed in a container, and then water 9931 was added, stirred for 40 minutes, and thoroughly kneaded. 257V (as described above) was added and stirred for 15 minutes to sufficiently suspend the mixture to obtain a sputter adhesion inhibitor.

実施例4 実施例1と同じ設備を用い、塩基性炭酸ジルコニウム1
202を容器に入れ、次に水9Qfを加えて、撹拌を4
0分間行い充分混線を行った後、1号ケイ酸カリ(JT
S規格品)39とアロロン580(前出)252と水5
7gを加え、15分間撹拌を行い懸濁させ、スパッタ付
着防止剤を得た。
Example 4 Using the same equipment as in Example 1, basic zirconium carbonate 1
202 in a container, then add 9Qf of water and stir for 4 hours.
After 0 minutes and sufficient crosstalk, No. 1 potassium silicate (JT
S standard product) 39, Aroron 580 (mentioned above) 252 and water 5
7 g was added and stirred for 15 minutes to suspend, thereby obtaining a sputter adhesion inhibitor.

実施例5 実施例1と同じ設備を用い、酸化ジルコニウム807、
重質炭酸カルシウム79りを容器に入れ、1.1.1 
)ジクロルエタン90fを加えて、撹拌を40分間行い
充分混練を行った後、残りの1.1.1トリクロルエタ
ン30f1ベツカサイト1100(アルキル変性樹脂、
商品名、大日本インキ化学工業柩)製)241を加え、
15分間撹拌を行い懸濁させ、スパッタ付着防止剤を得
た。
Example 5 Using the same equipment as in Example 1, zirconium oxide 807,
Put 79 grams of heavy calcium carbonate into a container, 1.1.1
) Add 90 f of dichloroethane, stir for 40 minutes, and thoroughly knead.
Add product name, Dainippon Ink Kagaku Kogyo Hitsugi) 241,
The suspension was stirred for 15 minutes to obtain a sputter adhesion inhibitor.

実施例6 実施例1と同じ設備を用い、酸化ジルコニウム45f1
重質炭酸カルシウム451を容器に入れ、トリクロルエ
チレン1202を加えて、撹拌を40分間行い充分混線
を行った後、トリクロルエチレン6847、ベラカサイ
ト1100(前出)17.12を加え15分間撹拌を行
い懸濁させ、スパッタ付着防止剤を得た。
Example 6 Using the same equipment as Example 1, zirconium oxide 45f1
Place heavy calcium carbonate 451 in a container, add trichlorethylene 1202, stir for 40 minutes to ensure sufficient crosstalk, then add trichlorethylene 6847 and veracasite 1100 (mentioned above) 17.12 and stir for 15 minutes and suspend. The mixture was made cloudy to obtain a sputter adhesion inhibitor.

実施例7 実施例1と同じ設備を用い、水酸化ジルコニウム48.
9f、塩基性炭酸ジルコニウム48.9f。
Example 7 Using the same equipment as in Example 1, zirconium hydroxide 48.
9f, basic zirconium carbonate 48.9f.

重質炭酸カルシウム6fを容器に入れ、1,1.1 ト
リクロルエタン1209を加えて、撹拌を40分間行い
充分混練を行った後、1,1.1 ) IJジクロルタ
ン58.5 f、ベラカサイト1100(前出)17.
IVを加え、15分間撹拌を行い懸濁させ、スパッタ付
着防止剤を得た。
Place 6 f of heavy calcium carbonate in a container, add 1,1.1 trichloroethane 1209, stir for 40 minutes and thoroughly knead, then add 1,1.1) IJ dichlorothane 58.5 f, veracasite 1100 ( Previous) 17.
IV was added and stirred for 15 minutes to suspend the mixture to obtain a sputter adhesion inhibitor.

実施例8 実施例1と同じ設備を用い、酸化ジルコニウム402、
水酸化ジルコニウム40f1シリカ26−9 = y、酸化チタン62、重質炭酸カルシウム20y1チレ
ン302、ペラカサイト1100(前出)27Vを加え
、15分間撹拌を行い懸濁させ、スパッタ付着防止剤を
得た。
Example 8 Using the same equipment as in Example 1, zirconium oxide 402,
Zirconium hydroxide 40f1 silica 26-9=y, titanium oxide 62, heavy calcium carbonate 20y1 tyrene 302, and peracasite 1100 (described above) 27V were added and stirred for 15 minutes to suspend, thereby obtaining a spatter adhesion inhibitor.

比較例1 実施例1と同じ設備を用い、酸化マグネシウム150 
f、酸化チタン302、重質炭酸カルシウム1.59を
容器に入れ、水1202を加えて、撹拌を50分間行い
充分混練を行い懸濁させ、スパッタ付着防止剤を得た。
Comparative Example 1 Using the same equipment as Example 1, magnesium oxide 150
f, 302 kg of titanium oxide, and 1.59 kg of heavy calcium carbonate were placed in a container, 120 kg of water was added, and the mixture was stirred for 50 minutes to thoroughly knead and suspend to obtain a spatter adhesion preventive agent.

2、ペラカサイト1100(前出)60ノを容器に入れ
、1,1.1 )ジクロルエタン180rを加、tて、
撹拌を50分間行い充分混練させ、スパッタ付着防止剤
を得た。
2.Pour 60 liters of Perakasite 1100 (mentioned above) into a container, add 180 liters of 1,1.1) dichloroethane, and
Stirring was performed for 50 minutes to thoroughly knead the mixture to obtain a spatter adhesion inhibitor.

スパッタ付着防止剤の性能評価試験 表面をサンダー加工した、大きさが400X165−1
0= ×19間の軟鋼(8841)を母材として用い、突き合
せた母材の両側約150咽と開先部に実施例1〜8、比
較例1〜2のスパッタ付着防止剤をそれぞれ塗布し、風
乾1時間の後、溶接ワイヤ(JIS  Y  eW、径
1.2鱈φ)を用いて、溶接電流260 A、溶接電圧
25v1溶着金属6層の溶接条件で炭酸ガスアーク溶接
を行なった。溶接完了後、スパッタ付着防止剤塗布面の
塗膜状況および全長400喘にわたる溶接線付近のスパ
ッタ付着数を調べ、さらに開先面に塗布したスパッタ付
着防止剤の影響を、X線透過法によって溶着金属中のピ
ット、ブロホールの数を測定して調べた。これらの結果
は表1に示す通りである。
Performance evaluation test of anti-spatter adhesion agent Surface sanded, size 400 x 165-1
Mild steel (8841) between 0 = ×19 was used as the base material, and the anti-spatter adhesion agents of Examples 1 to 8 and Comparative Examples 1 to 2 were applied to approximately 150 mm on both sides of the butted base material and the groove part. After air-drying for 1 hour, carbon dioxide arc welding was performed using a welding wire (JIS Y eW, diameter 1.2 φ) under welding conditions of 260 A welding current, 25v1 welding voltage, and 6 layers of deposited metal. After welding is completed, the condition of the coating film on the surface coated with spatter adhesion prevention agent and the number of spatter adhesion near the weld line over the entire length of 400 mm are investigated, and the influence of the spatter adhesion prevention agent applied to the groove surface is investigated using X-ray transmission method. The number of pits and blowholes in the metal was measured and investigated. These results are shown in Table 1.

表1に示されるように実施例1〜8は、塗膜のはく離が
無く密着性が良好で、又スパッタの付着もなく、また溶
着金属のピット、ブロホールも々くX線透過試験は1級
であった。
As shown in Table 1, Examples 1 to 8 had good adhesion with no peeling of the paint film, no adhesion of spatter, and no pits or blowholes in the weld metal, and the X-ray transmission test was grade 1. Met.

比較例1〜2は、溶接線付近に部分はく離や一部はく離
があり、スパッタも付着して除去が困難であった。また
、比較例2は良好であったが比較例1は溶着金属にピッ
ト、ブロホールがありX線透過試験は2級であった。
In Comparative Examples 1 and 2, there was partial peeling and peeling near the weld line, and spatter was also attached and difficult to remove. Further, Comparative Example 2 had good results, but Comparative Example 1 had pits and blowholes in the welded metal, and the X-ray transmission test was grade 2.

表  1 *I  JIS  Z  2343による特許出願人 
 日本油脂株式会社
Table 1 *I Patent applicant according to JIS Z 2343
Nihon Yushi Co., Ltd.

Claims (1)

【特許請求の範囲】[Claims] 酸化ジルコニウムまたは加熱によって酸化ジルコニウム
を生成するジルコニウム化合物を有効成分とするスパッ
タ付着防止剤
A sputter adhesion prevention agent whose active ingredient is zirconium oxide or a zirconium compound that generates zirconium oxide when heated.
JP2573883A 1983-02-18 1983-02-18 Anti-spatter agent Pending JPS59150666A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP2573883A JPS59150666A (en) 1983-02-18 1983-02-18 Anti-spatter agent

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP2573883A JPS59150666A (en) 1983-02-18 1983-02-18 Anti-spatter agent

Publications (1)

Publication Number Publication Date
JPS59150666A true JPS59150666A (en) 1984-08-28

Family

ID=12174155

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2573883A Pending JPS59150666A (en) 1983-02-18 1983-02-18 Anti-spatter agent

Country Status (1)

Country Link
JP (1) JPS59150666A (en)

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS62103923A (en) * 1985-10-30 1987-05-14 オムロン株式会社 Limit switch
EP1385636A1 (en) * 2001-03-30 2004-02-04 J & G Chemical Specialties Barrier coatings
WO2007050689A1 (en) * 2005-10-25 2007-05-03 Nd Industries, Inc. Protective coating and coated welding tip and nozzle assembly
JP2012081492A (en) * 2010-10-08 2012-04-26 Tsuchiya Co Ltd Spatter adhesion preventive agent
JP2014126060A (en) * 2012-12-25 2014-07-07 Pdm Co Ltd Adhesive insulation composition

Cited By (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS62103923A (en) * 1985-10-30 1987-05-14 オムロン株式会社 Limit switch
EP1385636A1 (en) * 2001-03-30 2004-02-04 J & G Chemical Specialties Barrier coatings
US6811821B2 (en) 2001-03-30 2004-11-02 J & G Chemical Specialities, Llc Barrier coatings
EP1385636A4 (en) * 2001-03-30 2005-07-13 J & G Chemical Specialties Barrier coatings
WO2007050689A1 (en) * 2005-10-25 2007-05-03 Nd Industries, Inc. Protective coating and coated welding tip and nozzle assembly
JP2012081492A (en) * 2010-10-08 2012-04-26 Tsuchiya Co Ltd Spatter adhesion preventive agent
JP2014126060A (en) * 2012-12-25 2014-07-07 Pdm Co Ltd Adhesive insulation composition

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