JP2012081492A - Spatter adhesion preventive agent - Google Patents
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Abstract
Description
本発明は、鋼材等を溶接する際に飛散するスパッタが、溶接箇所の周辺部に付着するのを防止するための溶接スパッタ付着防止剤に関する。 TECHNICAL FIELD The present invention relates to a welding spatter adhesion preventive agent for preventing spatter scattered when welding a steel material or the like from adhering to a peripheral portion of a welding location.
溶接を行う際に発生する溶接スパッタが製品、または治具に付着し、溶接後にスパッタを剥離する作業が必要となる。
特許文献1にはケイ酸のアルカリ金属塩から選択される1種または2種以上の塩;フッ化物イオン、炭酸水素イオン;および不可溶のアルコール類またはその誘導体を水に配合し、適宜その他の添加物を加えた溶接スパッタ付着防止剤が提供されている。
特許文献2には無機物又は無機化合物の微粉末を含む溶接スパッタ付着防止剤で、更に、水;ジカルボン酸;金属水素化物;トリアゾール類、キレート剤、飽和脂肪酸、及び不飽和脂肪酸からなる群より選択される1以上の物質を含んで成る混合液を含む溶接スパッタ付着防止剤が提案されている。
特許文献3には、セラミックス被膜を形成する組成物および金属酸化物フィラーを添加したスパッタ付着防止剤が提案されている。
The welding spatter generated during welding adheres to the product or jig, and it is necessary to peel off the spatter after welding.
In Patent Document 1, one or more salts selected from alkali metal salts of silicic acid; fluoride ions, hydrogen carbonate ions; and insoluble alcohols or derivatives thereof are blended in water, and other types are appropriately added. Weld spatter adhesion inhibitors with additives are provided.
Patent Document 2 discloses a weld spatter adhesion inhibitor containing fine powders of inorganic substances or inorganic compounds, and further selected from the group consisting of water; dicarboxylic acids; metal hydrides; triazoles, chelating agents, saturated fatty acids, and unsaturated fatty acids. There has been proposed a weld spatter deposition inhibitor comprising a mixed liquid comprising one or more of the above-described substances.
Patent Document 3 proposes a composition for forming a ceramic film and a spatter adhesion preventing agent to which a metal oxide filler is added.
アーク溶接、スポット溶接、レーザー溶接などを行う際に、スパッタが飛び散り、製品及び周辺部材へ付着し、後工程にて付着したスパッタを取り除かなくてはならない。特に製品に付着しては、製品としての外観が損なわれるだけでなく、その製品を組み込んで最終製品として使用の際に付着したスパッタにより不具合の原因となり安定した製品製造ができない可能性がある。また、周辺部材に付着した際は、特に位置決めをする治具へ付着した場合、溶接の際に正確な位置決めができず、不良品を出す可能性が高くなる。したがって、ある程度溶接を行った後、タガネ等を用いて手作業にてスパッタを取り除く作業が実施されており、その除去作業に費やされる工数は甚大なものとなっているのが現状である。
特許文献1では製品への溶接スパッタの付着防止には効果があるが、周辺部材への付着防止効果には持続性がそれ程無いため、継続的、高頻度でのスパッタ付着防止剤の塗布が必要となる。
特許文献2では特許文献1よりもスパッタの付着防止効果に対してより強化されているものの、周辺部材への付着防止効果には持続性に関しては特に変わらない。
特許文献3ではスパッタ付着防止効果に対して強化されているが、溶接部近傍のより過酷な溶接条件ではその効果は低くなり、持続性はそれに伴い短くなってしまう。また、ケイ素を用いたスパッタ付着防止剤においては、塗装ハジキなどの他工程への悪影響が懸念され、使用現場では敬遠されやすい。
When performing arc welding, spot welding, laser welding, etc., spatter scatters and adheres to the product and peripheral members, and the spatter adhered in the subsequent process must be removed. In particular, when the product adheres to the product, not only the appearance of the product is impaired, but there is a possibility that the product may not be stably manufactured due to the spatter that is attached when the product is incorporated and used as a final product. Moreover, when adhering to a peripheral member, especially when adhering to a jig for positioning, accurate positioning cannot be performed at the time of welding, and the possibility of producing a defective product increases. Therefore, after performing welding to some extent, an operation of removing spatters manually using a chisel or the like is performed, and the number of man-hours spent for the removal operation is enormous.
Patent Document 1 is effective in preventing welding spatter from adhering to products, but the effect of preventing adhering to peripheral members is not very durable, so it is necessary to continuously and frequently apply an anti-spatter agent. It becomes.
In Patent Document 2, although the effect of preventing spatter adhesion is strengthened compared to Patent Document 1, the effect of preventing adhesion to peripheral members is not particularly changed with respect to sustainability.
In Patent Document 3, the effect of preventing spatter adhesion is strengthened, but the effect becomes lower under severer welding conditions in the vicinity of the welded portion, and the sustainability is shortened accordingly. In addition, the spatter adhesion preventive agent using silicon is likely to be adversely affected on other processes such as paint repelling, and is easily avoided at the site of use.
上記問題点を解決するため、本発明は、無機系被膜形成液を含む、スパッタ付着防止剤を提供する。 In order to solve the above-mentioned problems, the present invention provides a spatter adhesion preventing agent containing an inorganic film forming liquid.
本発明において用いられる無機系被膜形成液としては、式(1)で表される化合物の加水分解・重縮合物を含む無機系被膜形成液が含まれる。
Mp+(OR1)qR2 p−q (1)
(式中、Mは、Al、Zr及びTiからなる群から選択される少なくとも1種の元素であり;R1は炭素数1〜5個の炭化水素基、アルコキシアルキル基、又はアシル基であり;R2はビニル、アミノ、イミノ、エポキシ、アクリロイルオキシ、メタクリロイルオキシ、フェニル、メルカプト及びアルキル基からなる群から選択される少なくとも1種の有機基であり;pはMの価数を表し;qはOR1基の数を表し;p及びqはいずれも整数であり;p≧qである。)
The inorganic film forming liquid used in the present invention includes an inorganic film forming liquid containing a hydrolysis / polycondensate of the compound represented by the formula (1).
M p + (OR 1 ) q R 2 p-q (1)
Wherein M is at least one element selected from the group consisting of Al, Zr and Ti; R 1 is a hydrocarbon group having 1 to 5 carbon atoms, an alkoxyalkyl group, or an acyl group R 2 is at least one organic group selected from the group consisting of vinyl, amino, imino, epoxy, acryloyloxy, methacryloyloxy, phenyl, mercapto and alkyl groups; p represents the valence of M; Represents the number of OR 1 groups; p and q are both integers; p ≧ q.)
上記Mp+(OR1)qR2 p−qで表される化合物のうち、MがAlである化合物としては、アルミニウムトリイソプロポキシド、アルミニウムn−ブトキシド、アルミニウムトリt−ブトシキド、アルミニウムトリエトキシドなどが挙げられ、MがZrである化合物としては、ジルコニウムn−プロポキシド、ジルコニウムn−ブトキシド、ジルコニウムi−ブトキシド、ジルコニウムt−ブトキシド、ジルコニウムジメタクリレートジブトキシドなどが挙げられ、MがTiである化合物としては、チタンテトライソプロポキシド、チタンテトラn−ブトキシド、チタンテトラi−ブトキシド、チタンメタクリレートトリイソプロポキシド、チタンテトラメトキシプロポキシド、チタンテトラn−プロポキシド、チタンテトラエトキシドなどが挙げられる。これらの化合物のうち1種類だけを用いてよいが、二種類以上を混合してもかまわない。
式(1)の化合物の加水分解・重縮合反応は、例えば特開2001−214093に記載されているような公知の方法によって行うことができる。
加水分解・重縮合反応を行うために添加する水の量は、式(1)の化合物1モルに対して0.1モル以上が好ましい。
式(1)の化合物を加水分解・縮重合する際には、既知の触媒などを添加して加水分解・縮重合を促進しても良い。この場合、添加する触媒としては、酢酸、プロピオン酸、酪酸などの有機酸や、硝酸、塩酸、リン酸、硫酸などの無機酸を用いることができる。
Among the compounds represented by M p + (OR 1 ) q R 2 p-q , the compound in which M is Al includes aluminum triisopropoxide, aluminum n-butoxide, aluminum tri-t-butoxide, aluminum triethoxy. Examples of the compound in which M is Zr include zirconium n-propoxide, zirconium n-butoxide, zirconium i-butoxide, zirconium t-butoxide, zirconium dimethacrylate dibutoxide, and the like. Some compounds include titanium tetraisopropoxide, titanium tetra n-butoxide, titanium tetra i-butoxide, titanium methacrylate triisopropoxide, titanium tetramethoxypropoxide, titanium tetra n-propoxide, titanium tetraeth Sid and the like. Only one of these compounds may be used, but two or more may be mixed.
The hydrolysis and polycondensation reaction of the compound of the formula (1) can be performed by a known method as described in, for example, JP-A-2001-214093.
The amount of water added to perform the hydrolysis / polycondensation reaction is preferably 0.1 mol or more per 1 mol of the compound of the formula (1).
When the compound of formula (1) is subjected to hydrolysis / condensation polymerization, a known catalyst or the like may be added to promote hydrolysis / condensation polymerization. In this case, as the catalyst to be added, organic acids such as acetic acid, propionic acid and butyric acid, and inorganic acids such as nitric acid, hydrochloric acid, phosphoric acid and sulfuric acid can be used.
上記Mp+(OR1)qR2 p−qの加水分解・重縮合物は、好ましくは液状である。しかし、固体状の加水分解・重縮合物でも溶媒添加により液状となるものであれば使用することができる。 The hydrolysis / polycondensation product of M p + (OR 1 ) q R 2 p-q is preferably liquid. However, solid hydrolyzate / polycondensate can be used as long as it becomes liquid by addition of a solvent.
スパッタ付着防止剤を上記のような組成とすることにより、次のような有利な効果が得られる。すなわち、スパッタ付着防止剤を塗布した際には図1に示すような構造で有機基が残っており、その後の除去する際には有機溶剤類で除去が可能である。また溶接の近傍でスパッタが当たる部分では被膜に熱がかかり、セラミックス被膜が形成されて強度が向上し耐久性が高くなる。 By setting the spatter adhesion preventing agent to the above composition, the following advantageous effects can be obtained. That is, when the spatter adhesion preventing agent is applied, the organic group remains in the structure as shown in FIG. 1 and can be removed with an organic solvent during subsequent removal. Further, heat is applied to the coating at the portion where the spatter hits in the vicinity of welding, and a ceramic coating is formed to improve the strength and increase the durability.
また、上記スパッタ付着防止剤へ助剤としてセラミックスフィラーもしくはセラミックスゾルを適宜添加しても良い。セラミックスフィラーとして、アルミナ、ジルコニア、チタニア等の酸化物や窒化ホウ素、窒化アルミニウム等の窒化物及び炭化ケイ素、タングステンカーバイト等炭化物などがあり、1種以上組み合わせて添加してもよい。フィラーは単体で添加しても良いし、分散液(スラリー)の状態で添加しても良い。また、セラミックスフィラーの分散性を向上させるため、界面活性剤などの分散剤を添加しても良い。セラミックスゾルとしてはシリカゾル、アルミナゾル、チタニアゾル、ジルコニアゾル等があり、1種以上組み合わせて添加してもよい。 Further, a ceramic filler or a ceramic sol may be appropriately added as an auxiliary agent to the spatter adhesion preventing agent. Examples of the ceramic filler include oxides such as alumina, zirconia, and titania, nitrides such as boron nitride and aluminum nitride, and carbides such as silicon carbide and tungsten carbide, and one or more may be added in combination. The filler may be added alone or in the form of a dispersion (slurry). In order to improve the dispersibility of the ceramic filler, a dispersant such as a surfactant may be added. Examples of the ceramic sol include silica sol, alumina sol, titania sol, zirconia sol, and the like.
また、スパッタ付着防止剤の溶媒としては、特に指定されるものではないが、塗布後の乾燥性を考慮し、エタノール、イソプロパノール、1−プロパノール等のアルコール類、アルコキシエタノール類、エチレングリコールモノアルキルエーテル類、プロピレングリコール類、等が好ましい。 Moreover, the solvent for the spatter adhesion preventing agent is not particularly specified, but considering the drying property after coating, alcohols such as ethanol, isopropanol and 1-propanol, alkoxyethanols, ethylene glycol monoalkyl ether And propylene glycols are preferred.
さらに、スパッタ付着防止剤の塗布性・作業性の向上のため、粘度を調整してもよい。粘度調整の方法としては、フィラー濃度で調整してもよいし、溶媒種類で調整してもよい。また増粘剤を適量添加してもよい。 Furthermore, the viscosity may be adjusted in order to improve the coating property and workability of the spatter adhesion preventing agent. As a method for adjusting the viscosity, the viscosity may be adjusted by the filler concentration or the solvent type. An appropriate amount of thickener may be added.
スパッタ付着防止剤の塗布方法は特に指定されるものではないが、必要な箇所へ刷毛塗り、スプレー塗布等が好ましい。また、このスパッタ付着防止剤はエアゾール化も可能であり、前もってエアゾール化することにより溶接機の設置環境によらず塗布が可能となる。 The method for applying the spatter adhesion preventing agent is not particularly specified, but brushing, spraying, etc. are preferably applied to the necessary portions. Further, the spatter adhesion preventing agent can be aerosolized, and can be applied regardless of the installation environment of the welding machine by aerosolizing in advance.
また上記スパッタ付着防止剤に着色を施してもよい。溶接現場での注意喚起や製造工程上の識別等のために、塗布した部分に着色を施し区別する必要がある際にコート被膜に着色してあると識別とスパッタ付着防止の2つの効果を同時に付与することができる。例えば、着色を施す方法として着色剤を添加し所望の色を加える。着色剤として無機顔料、有機顔料及び有機染料などが挙げられる。有機顔料や有機染料ではスパッタにより一部燃焼してしまい色褪せや焦げ付きなどが発生するが、再度塗布するタイミングを計る上での参考となる。 Further, the spatter adhesion preventing agent may be colored. When it is necessary to color and distinguish the applied part for alerting at the welding site or identification in the manufacturing process, the coating film is colored and the two effects of identification and spatter adhesion prevention are simultaneously achieved. Can be granted. For example, as a method of coloring, a colorant is added and a desired color is added. Examples of the colorant include inorganic pigments, organic pigments, and organic dyes. Organic pigments and organic dyes burn partly due to spattering and cause fading or scorching. This is useful for measuring the timing of re-application.
本発明のスパッタ付着防止剤を用いれば、溶接にて発生するスパッタの製品及び周辺部材へ付着を防止することができる。 If the spatter adhesion preventing agent of the present invention is used, it is possible to prevent adhesion to sputtered products and peripheral members generated by welding.
本発明のスパッタ付着防止剤を製品及び周辺部材へ塗布・乾燥することにより、セラミックス被膜を形成し、溶接スパッタが付着しにくくなる。そのため、セラミックス被膜が破壊され取り除かれない限り、スパッタ付着防止効果が持続する。 By applying and drying the spatter adhesion preventive agent of the present invention to the product and peripheral members, a ceramic film is formed and welding spatter is less likely to adhere. Therefore, as long as the ceramic coating is not destroyed and removed, the effect of preventing spatter adhesion continues.
しかしながら、このセラミックス被膜は乾燥しているが焼き付け工程を通してないため、アルコール類やケトン類、グリコールエーテル類などの有機溶剤により簡単に除去できる。したがって、製品へスパッタ付着防止剤を塗布してもその後に除去が可能となり製品の後工程に影響を与えることがない。 However, since this ceramic film is dry but does not pass through the baking process, it can be easily removed with an organic solvent such as alcohols, ketones or glycol ethers. Therefore, even if the spatter adhesion preventing agent is applied to the product, it can be removed thereafter without affecting the subsequent process of the product.
したがって、溶接機の周辺部材だけでなく、製品への適用も可能であり、スパッタが飛来する箇所の部材全てに適している。 Therefore, it can be applied not only to the peripheral members of the welding machine but also to products, and is suitable for all members where spatters fly.
また、本来は透明な被膜を形成するが、無機材料粒子を添加することにより、有色化するため塗布した際に塗布部を認識することができる。有色化を嫌う場合には、添加フィラーを無くしても良いし、ナノサイズのフィラーを添加することにより透明を維持したままのスパッタ付着防止剤が調製できる。 In addition, a transparent film is originally formed, but by adding inorganic material particles, the coated portion can be recognized when coated for coloring. When coloration is disliked, the additive filler may be eliminated, and by adding a nano-size filler, a spatter adhesion preventing agent that maintains transparency can be prepared.
以上のように、本発明のスパッタ付着防止剤は上述の従来の問題点をすべて解決するものである。 As described above, the spatter adhesion preventive agent of the present invention solves all the conventional problems described above.
以下に例を挙げるが、それらは本発明の説明を目的とするものであって、本発明をこれらの態様に限定することを意図するものではない。 The following examples are given for the purpose of illustrating the invention and are not intended to limit the invention to these embodiments.
<スパッタ付着性の評価>
スパッタ付着性の評価は図2に示す概略図のように塗布部から10mm離れた部分をアーク溶接し、溶接スパッタが付着するまで繰り返し実施した。溶接条件としてはわざとスパッタが多く出るように条件設定をした(表1)。被着体としてSPCC鋼材を用いて、一般鋼材としてSS鋼材を用いた。
<Evaluation of spatter adhesion>
As shown in the schematic diagram of FIG. 2, the sputter adherence evaluation was repeatedly performed until a portion 10 mm away from the coating portion was arc-welded and welding spatter adhered. The welding conditions were intentionally set so that a lot of spatter was generated (Table 1). SPCC steel was used as the adherend, and SS steel was used as the general steel.
<実施例1>
ジエタノールアミン18.4gに1−プロパノール(以下、nPAという)49.7g加え攪拌した後、ジルコニウムn−プロポキシド/nPA(70%/30%)溶液を49.7g加え更に攪拌した。そこへnPAとイオン交換水を重量比10:1で混合した溶液を22.3g加え、更に予めnPA28.4gに窒化ホウ素フィラー7.1gを添加し、ヒドロキシプロピルセルロース1.8gを溶解した溶液36.1gを加え攪拌した。その後ろ過を行い、スパッタ付着防止剤を得た。このスパッタ付着防止剤を市販の霧吹きノズルにて被着体へ塗布し、常温にて10分間乾燥を行った。
<Example 1>
After 49.7 g of 1-propanol (hereinafter referred to as nPA) was added to 18.4 g of diethanolamine and stirred, 49.7 g of a zirconium n-propoxide / nPA (70% / 30%) solution was added and further stirred. 22.3 g of a solution in which nPA and ion-exchanged water were mixed at a weight ratio of 10: 1 was added thereto, and 7.1 g of boron nitride filler was added to 28.4 g of nPA in advance to dissolve 1.8 g of hydroxypropylcellulose. 0.1 g was added and stirred. Thereafter, filtration was performed to obtain a spatter adhesion preventing agent. This spatter adhesion inhibitor was applied to an adherend with a commercially available spray nozzle and dried at room temperature for 10 minutes.
<実施例2>
実施例1と同様に調製したスパッタ付着防止剤をスプレー缶へ採取し、同体積のジメチルエーテルを充填し、エアゾール型スパッタ付着防止剤を得た。このエアゾール型スパッタ付着防止剤は噴射ガス(ジメチルエーテル)と混合した際に分離や凝集することなく、スプレーすることができた。このスパッタ付着防止剤を被着体へ塗布し、常温にて10分間乾燥を行った。
<Example 2>
The spatter adhesion inhibitor prepared in the same manner as in Example 1 was collected in a spray can and filled with the same volume of dimethyl ether to obtain an aerosol type spatter adhesion inhibitor. This aerosol-type spatter adhesion inhibitor could be sprayed without separation or aggregation when mixed with a propellant gas (dimethyl ether). This spatter adhesion preventing agent was applied to the adherend and dried at room temperature for 10 minutes.
<実施例3>
チタンテトライソプロポキシド156.3gにジエタノールアミン115.65gを加え、nPAで630mlまでメスアップを行った。その後100℃で3時間攪拌を行い、nPAとイオン交換水を重量比10:1で混合した溶液を200ml添加し更に攪拌を行った。その後、アルミナ粒子(粒径0.2μm)を25g添加し、ボールミル(ジルコニアボール2mmφ)で5時間分散処理を実施し、ろ過を行い、スパッタ付着防止剤を得た。このスパッタ付着防止剤を刷毛で被着体へ塗布し、常温にて10分間乾燥した。
<Example 3>
115.65 g of diethanolamine was added to 156.3 g of titanium tetraisopropoxide, and the volume was increased to 630 ml with nPA. Thereafter, the mixture was stirred at 100 ° C. for 3 hours, and 200 ml of a solution in which nPA and ion-exchanged water were mixed at a weight ratio of 10: 1 was added and further stirred. Thereafter, 25 g of alumina particles (particle size: 0.2 μm) was added, and dispersion treatment was performed for 5 hours with a ball mill (zirconia ball 2 mmφ), followed by filtration to obtain a spatter adhesion preventive agent. This spatter adhesion preventing agent was applied to the adherend with a brush and dried at room temperature for 10 minutes.
<比較例1>
特許文献3に記載の実施例1と同様に、グリシドキシプロピルトリメトキシシラン9.5gにメチルトリエトキシシラン17.8g及びオルトケイ酸テトラエチル20.8gを加え、その後酸性アルミナゾル(日産化学製)を41.4g加え、ボールミルにて24時間攪拌・分散を実施した。こうして得られたスパッタ付着防止剤を他の実施例と同様に溶接を実施し評価した。また、市販されている霧吹きノズルで塗布を行い、常温にて30分乾燥した。
<Comparative Example 1>
Similarly to Example 1 described in Patent Document 3, 17.8 g of methyltriethoxysilane and 20.8 g of tetraethyl orthosilicate were added to 9.5 g of glycidoxypropyltrimethoxysilane, and then acidic alumina sol (manufactured by Nissan Chemical Co., Ltd.) was added. 41.4 g was added and the mixture was stirred and dispersed in a ball mill for 24 hours. The sputter adhesion inhibitor thus obtained was evaluated by welding as in the other examples. Moreover, it apply | coated with the commercially available spray nozzle and dried for 30 minutes at normal temperature.
<比較例2>
市販のエアゾールタイプのスパッタ付着防止剤(トラスコ中山製、αスパッタクリン トーチノズル用)を被着体へ塗布し、他の実施例と同様に溶接を実施し評価した。
<Comparative example 2>
A commercially available aerosol type anti-sputtering agent (manufactured by Trusco Nakayama, for α-sputter clean torch nozzle) was applied to the adherend, and welding was performed and evaluated in the same manner as in the other examples.
表2より、実施例1〜3では繰り返し回数は20回以上でも溶接スパッタの付着は見られない。比較例では数回の繰り返しで溶接スパッタが付着しており、従来に比べ格段にスパッタ付着防止性が向上していることが確認できた。 From Table 2, in Examples 1 to 3, adhesion of weld spatter is not observed even when the number of repetitions is 20 times or more. In the comparative example, welding spatter was adhered several times, and it was confirmed that the spatter adhesion preventing property was remarkably improved as compared with the conventional example.
Claims (4)
Mp+(OR1)qR2 p−q
(式中、MはAl、Zr及びTiからなる群から選択される少なくとも1種の元素であり;pはMの価数を表わし;R1は炭素数1〜5の炭化水素基、アルコキシアルキル基またはアシル基であり;R2はビニル、アミノ、イミノ、エポキシ、アクリロイルオキシ、メタクリロイルオキシ、フェニル、メルカプト及びアルキル基からなる群から選択される少なくとも1種の有機基であり;qはOR1基の数を表し;p及びqはいずれも整数であり;p≧qである。)
で表わされる化合物の加水分解・重縮合物を含む、請求項1記載のスパッタ付着防止剤 The inorganic film forming liquid is
M p + (OR 1 ) q R 2 p-q
Wherein M is at least one element selected from the group consisting of Al, Zr and Ti; p represents the valence of M; R 1 is a hydrocarbon group having 1 to 5 carbon atoms, alkoxyalkyl R 2 is at least one organic group selected from the group consisting of vinyl, amino, imino, epoxy, acryloyloxy, methacryloyloxy, phenyl, mercapto and alkyl groups; q is OR 1 Represents the number of groups; p and q are both integers; p ≧ q.)
The spatter adhesion preventing agent according to claim 1, comprising a hydrolyzate / polycondensate of the compound represented by the formula:
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WO2019221117A1 (en) | 2018-05-18 | 2019-11-21 | オムロン株式会社 | Electronic article and method for forming film on electronic article |
CN111215774A (en) * | 2020-01-10 | 2020-06-02 | 汎宇化学(昆山)有限公司 | Method for preventing welding slag in welding process |
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CN112118962A (en) * | 2018-05-18 | 2020-12-22 | 欧姆龙株式会社 | Electronic article and film forming method for electronic article |
CN111215774A (en) * | 2020-01-10 | 2020-06-02 | 汎宇化学(昆山)有限公司 | Method for preventing welding slag in welding process |
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