JPS61132293A - Adhesion preventing medium of welding spatter - Google Patents

Adhesion preventing medium of welding spatter

Info

Publication number
JPS61132293A
JPS61132293A JP25423184A JP25423184A JPS61132293A JP S61132293 A JPS61132293 A JP S61132293A JP 25423184 A JP25423184 A JP 25423184A JP 25423184 A JP25423184 A JP 25423184A JP S61132293 A JPS61132293 A JP S61132293A
Authority
JP
Japan
Prior art keywords
welding
adhesion
spatter
water
resin
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
JP25423184A
Other languages
Japanese (ja)
Inventor
Masayuki Kawamoto
川本 誠之
Kazuyuki Hamada
浜田 和行
Shiro Isozaki
磯崎 志郎
Makoto Yaegashi
誠 八重樫
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.)
Mitsui Toatsu Chemicals Inc
Original Assignee
Mitsui Toatsu Chemicals Inc
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 Mitsui Toatsu Chemicals Inc filed Critical Mitsui Toatsu Chemicals Inc
Priority to JP25423184A priority Critical patent/JPS61132293A/en
Publication of JPS61132293A publication Critical patent/JPS61132293A/en
Pending legal-status Critical Current

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  • Paints Or Removers (AREA)
  • Nonmetallic Welding Materials (AREA)
  • Compositions Of Macromolecular Compounds (AREA)

Abstract

PURPOSE:To show an excellent effect in preventing a rust and spatter adhesion by making a welding spatter adhesion preventing medium from the water insoluble acrylic ester or metacrylic ester polymer body resin emulsion of specified composition. CONSTITUTION:It is the preventing medium from the adhesion of welding spatters containing 3-50wt% lower alkyl alcohol and consisting of the water insoluble acrylic ester or metacrylic ester polymer body resin emulsion of 3-50wt% solid part resin. By coating this welding spatters adhesion preventing material on the part to be welded of a steel material prior to the welding an elaborate film is formed and the spatter adhesion preventing effect excellent at welding time having an excellent rust prevention effect is brought on.

Description

【発明の詳細な説明】 (産業上の利用分野) 本発明は、鋼材の溶接作業時に用いられる溶接スパッタ
ーの付着防止剤に関する。
DETAILED DESCRIPTION OF THE INVENTION (Field of Industrial Application) The present invention relates to a weld spatter adhesion prevention agent used during welding work of steel materials.

(従来の技術) 従来、溶接スパッターの付着を防止する方法としてはス
ケ−リングツ・ンマーなどによる手作業によっていた。
(Prior Art) Conventionally, as a method for preventing the adhesion of welding spatter, manual operation using a scaling tool or the like has been used.

しかし、この方法では作業時間、作業効率、作業員の疲
労などの点で箸し℃・欠点を有 。
However, this method has disadvantages in terms of work time, work efficiency, worker fatigue, etc.

している。また鋼材の被溶接部周辺に塗布してスパッタ
ーの付着防止を行うような処理剤として次のような例が
ある。例えばフェノール系、アルキッド系、ポリウレタ
ン系、尿素系、メラミン系等の合成樹脂と有機溶剤とを
配合した塗料状のスパッター付着防止剤(特公昭42−
129Lアルキツド樹脂に酸化カルシウムと酸化第二鉄
の複合焼結粉末体を添加したスパッター付着防止剤(特
開昭52−44745)など合成樹脂を溶剤に溶解させ
た、或いはそれらに耐熱性を持たせるため無機フィラー
を添加したもの等である。したがって、これらの組成物
を使用すると、塗布時の有機溶剤の飛散による火災の発
生、臭気による作業環境の悪化等の問題が生じる。一方
、上記のような問題点を解決するため、不燃性である水
を溶媒としたスパッター付着防止剤がある。例えば、胡
粉、タルクに水溶性フェノール樹脂と界面活性剤とを配
合したペースト状のスパッター付着防止剤(特公昭46
−13810)、界面活性剤と防錆剤と一価アルコール
と水とを混合したスパッター付着防止剤(特公昭52−
23899)、特定のアルキッド樹脂またはアクリル樹
脂を相溶剤とともに水に可溶化したスパッター付着防止
剤(特開昭57−131270)である。
are doing. Further, there are the following examples of treatment agents that are applied to the periphery of the welded parts of steel materials to prevent spatter from adhering. For example, a paint-like spatter adhesion prevention agent containing a synthetic resin such as a phenol type, an alkyd type, a polyurethane type, a urea type, a melamine type, and an organic solvent (Special Publication No.
Synthetic resins are dissolved in solvents, such as sputter adhesion prevention agent (JP-A-52-44745), which is made by adding composite sintered powder of calcium oxide and ferric oxide to 129L alkyd resin, or they are made heat resistant. For this purpose, inorganic fillers are added. Therefore, when these compositions are used, problems such as fires caused by scattering of organic solvents during coating and deterioration of the working environment due to odors occur. On the other hand, in order to solve the above-mentioned problems, there is a sputter adhesion prevention agent using nonflammable water as a solvent. For example, a paste-like spatter adhesion prevention agent made by blending chalk, talc, water-soluble phenolic resin, and surfactant (Special Publication No. 46)
-13810), a sputter adhesion prevention agent mixed with a surfactant, a rust preventive, a monohydric alcohol, and water (Special Publication No. 52-
23899), a sputter adhesion prevention agent made by solubilizing a specific alkyd resin or acrylic resin in water together with a compatibilizer (Japanese Unexamined Patent Publication No. 57-131270).

(発明が解決しようとする問題点) 溶接においては被溶接面が錆びていな℃・ことが重要で
、錆びている場合は溶接強度が低下する等の不都合が生
じる。この点において前記の水を溶媒としたスパッター
付着防止剤は、鋼材へのスパッターの付着を防止する機
能は有するものの、水溶性のため、塗膜が水を保持しや
すく、その為溶接前に発錆して溶接に悪影響を及ぼす。
(Problems to be Solved by the Invention) In welding, it is important that the surface to be welded is not rusted, and if it is rusted, problems such as a decrease in welding strength will occur. In this regard, although the above-mentioned spatter adhesion prevention agent using water as a solvent has the function of preventing spatter adhesion to steel materials, since it is water-soluble, the coating film tends to retain water, so it is difficult to prevent spatter from forming before welding. It rusts and has a negative effect on welding.

また、上記したスパッター付着防止剤のうち、フィラー
を含むものは、塗膜表面が荒れているので、溶接後項材
表面を塗装する場合、スパッター付着防止剤を除去する
必要がある。
In addition, among the above-mentioned sputter adhesion preventive agents, those containing fillers have a rough coating surface, so when painting the surface of the material after welding, it is necessary to remove the spatter adhesion preventive agent.

本発明は、被溶接部に塗布することによりスパッターの
付着を防止し、形成された塗膜により発錆を防止し、さ
らに溶接後スパッター付着防止剤を除去することなく塗
装できるような溶接スパッター付着防止剤を提供するこ
とを目的とする。
The present invention prevents adhesion of spatter by applying it to the part to be welded, prevents rust from forming with the formed coating film, and further prevents adhesion of welding spatter so that it can be painted without removing the anti-spatter agent after welding. The purpose is to provide an inhibitor.

(問題点を解決するための手段) 本発明者は鋭意研究を重ねた結果、特定のアクリル41
4 脂エマルジョンに特定のアルコールを添加した組成
物を被溶接部に塗布すると、機密な皮膜が形成され、良
好なスパッター付着防止効果があり、防錆力を有し、さ
らに溶接後除去することな−く塗装し5ることを見出し
て本発明を完成するに至った。即ち本発明は3〜50重
量%の低級アルキルアルコールを含み、かつ樹脂固形分
が3〜50重唱[%である、水不溶性のアクリル酸エス
テル又はメタクリル酸エステル重合体樹脂エマルジョン
よりなる溶接スパッターの付着防止剤である。
(Means for solving the problem) As a result of extensive research, the inventor has found that a specific acrylic 41
4 When a composition made by adding a specific alcohol to a fat emulsion is applied to the part to be welded, a secret film is formed, which has a good spatter adhesion prevention effect, has anti-corrosion properties, and does not need to be removed after welding. The present invention has been completed by discovering that it is possible to coat the surface of the surface of the surface of the surface of the surface of the surface of the surface. That is, the present invention provides a method for welding spatter adhesion made of a water-insoluble acrylic ester or methacrylic ester polymer resin emulsion containing 3 to 50% by weight of lower alkyl alcohol and having a resin solid content of 3 to 50% by weight. It is an inhibitor.

本発明の付着防止剤を製造するには、例えばアクリル酸
エステル又はメタクリル酸エステル重合体樹脂エマルジ
ョンにアルコール、必要であればさらに水を加えること
によって得ることができる。
The anti-adhesive agent of the present invention can be produced, for example, by adding alcohol and, if necessary, water to an acrylic ester or methacrylic ester polymer resin emulsion.

このようなアクリル酸エステル又はメタクリル酸エステ
ル重合体樹脂エマルジョンは例えばアクリル酸メチル、
アクリル酸エチル、アクリル酸n−ブチル、アクリル酸
2−エチルヘキシル等のアクリル酸アルキルエステル、
メタクリル酸メチル、メタクリル酸エチル、メタクリル
en−ブチル、メタクリル酸2−エチルヘキシル等のメ
タクリル譚アルキルエステル、メタクリル酸グリシジル
、アクリル酸2−ヒドロキシエチル、メタクリル酸2−
ヒドロキシエチル等のアクリル酸エステル、メタクリル
酸エステルモノマーの単独重合体又は2種以上の共重合
体樹脂エマルジョン、又は前記モノマーと共重合し得る
ビニルモノマー、例えばスチレン、ビニルトルエン等の
芳香族ビニル化合物、α、β−不飽和カルボン酸、イタ
コン酸、マレイン酸、フマル酸等のα、β−不砲和二塩
基酸およびそのエステル化合物、酢酸ビニル、プロピオ
ン酸ビニル等のビニルアルコールのエステル化合物、ア
クリルアミド、メタクリルアミド、塩化ビニル等との共
重合体樹脂エマルジョンがあげられる。またこれらの重
合体、共重合体はそのガラス転移温度(以FT?と略称
する)が、0〜50℃であるものより選ばれるのが好ま
しい。T2がこの範囲であれば成膜性が優れ、塗膜の表
面が平滑となる。これらの重合体又は共重合体樹脂は水
不溶性であることが必要で、水溶性の場合には本発明の
目的である溶接前の防錆効果が発現しない。
Such acrylic ester or methacrylic ester polymer resin emulsions include, for example, methyl acrylate,
Acrylic acid alkyl esters such as ethyl acrylate, n-butyl acrylate, and 2-ethylhexyl acrylate;
Methyl methacrylate, ethyl methacrylate, en-butyl methacrylate, methacrylic tan alkyl esters such as 2-ethylhexyl methacrylate, glycidyl methacrylate, 2-hydroxyethyl acrylate, 2-methacrylate
A homopolymer or copolymer resin emulsion of two or more acrylic ester or methacrylic ester monomers such as hydroxyethyl, or a vinyl monomer that can be copolymerized with the above monomers, such as an aromatic vinyl compound such as styrene or vinyltoluene, α,β-unsaturated carboxylic acids, itaconic acid, maleic acid, fumaric acid and other α,β-unionated dibasic acids and their ester compounds; vinyl alcohol ester compounds such as vinyl acetate and vinyl propionate; acrylamide; Examples include copolymer resin emulsions with methacrylamide, vinyl chloride, etc. Further, these polymers and copolymers are preferably selected from those having a glass transition temperature (hereinafter abbreviated as FT?) of 0 to 50°C. If T2 is within this range, film forming properties will be excellent and the surface of the coating will be smooth. These polymer or copolymer resins must be water-insoluble; if they are water-soluble, they will not exhibit the rust-preventing effect before welding, which is the object of the present invention.

上記の樹脂エマルジョンは通常の乳化重合で得ることが
できる。乳化重合に際して用いられる乳化剤としては、
例えば、ラウリル硫酸ソーダ、ドデシルベンゼンスルホ
ン酸ンーダ等の陰イオン性乳化剤、あるいはポリオキシ
エチレンノニルフェニルエーテノペ、オキシエチレンオ
キシプロピレン共重合体等の非イオン性乳化剤等、通常
の乳化剤でよい。また重合開始剤としては通常のラジカ
ル重合開始剤が使用され、例えば過は化ベンゾイルで代
表されるような有機過酸化物、過硫酸アンモニウム、過
硫酸カリウム等の過硫酸塩、アゾビスイノブチロニトリ
ル等が代表的にあげられ、またメタ重亜硫酸カリウムや
チオ硫酸ナトリウム等の還元剤とともに使用するレドッ
クス系触媒でもよ(゛。
The above resin emulsion can be obtained by conventional emulsion polymerization. Emulsifiers used during emulsion polymerization include:
For example, conventional emulsifiers may be used, such as anionic emulsifiers such as sodium lauryl sulfate and dodecylbenzenesulfonate, or nonionic emulsifiers such as polyoxyethylene nonyl phenyl ether, oxyethylene oxypropylene copolymer, and the like. In addition, as the polymerization initiator, ordinary radical polymerization initiators are used, such as organic peroxides such as benzoyl peroxide, persulfates such as ammonium persulfate and potassium persulfate, and azobisinobutyronitrile. etc. are typical examples, and redox catalysts used together with reducing agents such as potassium metabisulfite and sodium thiosulfate may also be used.

本発明における低級アルキルアルコールとしてはメタノ
ール、エタノール、フロビルアルコールがあげられ、こ
れらは単独でも2種以上併用してもよし・。アルコール
の量は3〜50重量%(以下%は全て重量%とする)、
好ましくは5〜30%で、3%未満ではアルコール類に
よる成膜時の乾燥速度を早める効果がなくなり、逆て5
0%を越えると、アクリル嗣脂エマルジョンを安定に存
在させることができなくなる。なお必要に応じメチルエ
チルケト/等の低沸点溶剤をアルコールとともに使用し
てもよい。また塗膜の平滑性を良好にする目的でセロソ
ルフ゛、フ゛チルセロソルブール、ブチルカルピトール
、キシレン、ベンジルアルコール、プロピレングリコー
ルなどの中すいし高沸点溶剤を加えてもよし・。
Examples of lower alkyl alcohols in the present invention include methanol, ethanol, and flobyl alcohol, and these may be used alone or in combination of two or more. The amount of alcohol is 3 to 50% by weight (all percentages below are by weight),
Preferably it is 5 to 30%; if it is less than 3%, the effect of alcohols on accelerating the drying speed during film formation is lost;
If it exceeds 0%, the acrylic clot emulsion will not be able to exist stably. Note that, if necessary, a low boiling point solvent such as methyl ethyl keto/etc. may be used together with alcohol. In addition, medium to high boiling point solvents such as cellosol, methylcellosorbul, butylcarpitol, xylene, benzyl alcohol, and propylene glycol may be added to improve the smoothness of the coating film.

本発明の付着防止剤はその樹脂固形分が3〜50%であ
ることが必要である。3%未満では塗膜が薄くなるため
充分な防錆効果がでない。また50%をこえると粘度が
高くなり、塗工性が悪くなり、実用的でない。好ましい
樹脂固形分の範囲は5〜30%である。
The anti-adhesion agent of the present invention needs to have a resin solid content of 3 to 50%. If it is less than 3%, the coating film will become thin and will not have sufficient rust prevention effect. Moreover, if it exceeds 50%, the viscosity becomes high and coating properties deteriorate, making it impractical. The preferred range of resin solids is 5-30%.

本発明の付着防止剤を製造するには前記の樹脂エマルジ
ョンに前記アルコールを必要量加え、必要に応じ攪拌す
ればよい。樹脂エマルジョン中の1剥脂固形分は予め測
定しておき、最終的に付着防止剤の樹脂固形分濃度が所
定の範囲になるように水で調整する。
In order to produce the anti-adhesion agent of the present invention, the required amount of the alcohol may be added to the resin emulsion, and the mixture may be stirred if necessary. The solid content of 1 oil removed in the resin emulsion is measured in advance, and finally adjusted with water so that the resin solid content concentration of the anti-adhesion agent falls within a predetermined range.

本発明の付着防止剤は溶接前に吹き付けや刷毛塗り等、
通常の方法で被溶接部に塗工、乾燥して使用する。
The anti-adhesion agent of the present invention can be applied by spraying or brushing before welding.
Apply it to the part to be welded in the usual way, dry it, and use it.

(作 用) 上記した如(、本発明の溶接スパッター付着防止剤は、
それを鋼材の溶接に先立って、鋼材の被溶接部に塗布す
ることにより数奇な膜を形成し、防錆効果におし・て優
れ、溶接時においてすぐれたスパッター付着防止効果を
もたらすとともに、溶接後、該膜を除去することなく、
その上に塗装することを可能にした。特に水不溶性のア
クリル酸エステル又はメタクリル酸二。ステル重合体又
は共重合体樹脂のエマルジョンを主成分とする為、鋼材
に対する密着性がよ(、かつ塗膜は吸湿性が小さく、防
錆効果が一段と優れている。
(Function) As described above, the welding spatter adhesion inhibitor of the present invention
By applying it to the part of the steel material to be welded prior to welding, it forms a strange film that has an excellent rust prevention effect and provides an excellent spatter adhesion prevention effect during welding. After that, without removing the film,
It was possible to paint over it. Especially water-insoluble acrylic acid esters or dimethacrylic acid esters. Since the main component is an emulsion of stell polymer or copolymer resin, it has good adhesion to steel materials (and the coating film has low hygroscopicity, making it even more effective in preventing rust).

(実施例) 以下に実施例で説明する。なお試験片の作成および性能
試験は以下の方法で行った。
(Example) Examples will be described below. Note that the preparation of the test pieces and the performance test were conducted in the following manner.

樹脂固形分 JisK−s4ooに規定する乾燥残分の測定法に準じ
て測定した。
The resin solid content was measured according to the method for measuring dry residue specified in JISK-s4oo.

安定性 付着防止剤を60日間静置しエマルジョンが二層分離す
る程度により判定した。
The stability of the anti-adhesive agent was evaluated based on the extent to which the emulsion separated into two layers after being allowed to stand for 60 days.

乾燥性 刷毛塗り後の塗膜の乾燥速度を肉眼で観察した。dryness The drying speed of the coating film after brush application was observed with the naked eye.

針入法により測定した。It was measured by the needle penetration method.

受膜平滑性 試験片を肉眼で観察し判定した。membrane smoothness The test piece was visually observed and judged.

密着強度 試験片の塗膜に1u間隔で縦横各11本の切り込みを℃
・れ、セロノ・/テープを密着後、勢℃・よくはがして
、100イ固の盲目のうちはがれないものの割合を示し
た。
11 vertical and horizontal cuts were made in the coating film of the adhesion strength test piece at 1u intervals at °C.
・After adhering the tape, the tape was carefully peeled off and the percentage of 100 pieces of tape that did not come off was shown.

耐水性 試験片を48時間水に浸漬して、塗膜の白化状態を観察
した。
The water resistance test piece was immersed in water for 48 hours, and the whitening state of the coating film was observed.

発錆性 試験片を20°C、65%RHの雰囲気に放置し、1昼
夜経過後及び7昼夜経過後の錆の発生状況を観察した。
The rust development test pieces were left in an atmosphere of 20°C and 65% RH, and the state of rust generation was observed after one day and night and after seven days and nights.

塗装性 試験片の塗膜に市販の下塗り塗料を塗布して乾燥し、前
記の密着強度の試験に準じて、付着防止剤の塗膜と下塗
り塗料との密着強度を測定するとともに、塗膜の表面状
態を観察した。
A commercially available undercoat paint was applied to the paint film of the paintability test piece, dried, and the adhesion strength between the anti-adhesion agent paint film and the undercoat paint was measured according to the adhesion strength test described above. The surface condition was observed.

スパッター付着防止性 厚さ10朋の鋼板を突合せて開先面を形成させ、スパッ
ター付着防止剤を鋼板表面に塗布、乾燥し、低水素系溶
接棒を使用して、溶接電流150A、溶接電圧30V、
溶接速度1 ’5 0 mx1分で手溶接を行った。溶
接後、溶接部100uあたりのスパッター付着側数を測
定した。
Spatter adhesion prevention Steel plates with a thickness of 10 mm are butted together to form a groove surface, a spatter adhesion prevention agent is applied to the steel plate surface, dried, and a low hydrogen welding rod is used to weld at a welding current of 150 A and a welding voltage of 30 V. ,
Manual welding was performed at a welding speed of 1'50 m x 1 minute. After welding, the number of spatter-attached sides per 100 u of welded area was measured.

なお以下の実施例、比較例で部、%、割合は全て重量基
準とする。
In the following Examples and Comparative Examples, all parts, percentages, and ratios are based on weight.

実施例1 温度計、還流冷却器、攪拌機、モノマーチャージ器をつ
けた214ツロフラスコに水800部を入れ窒素気流下
70℃に昇温した。乳化剤としてラウリル硫酸ソーダ5
部、重合開始剤として過硫酸カリウム5部を加え、これ
にスチレン700部、アクリル酸ブチル470部、メタ
クリルl¥J!50部の混合モノマーを、3時間にわた
って連続的にフラスコ中に滴下した。その後さらに同温
度で2時間反応せしめ重合を完結させた。さらにアンモ
ニアおよびジメチルエタノールアミンによりpH9,0
とした。
Example 1 800 parts of water was placed in a 214 Turow flask equipped with a thermometer, reflux condenser, stirrer, and monomer charger, and the temperature was raised to 70° C. under a nitrogen stream. Sodium lauryl sulfate 5 as an emulsifier
1 part, 5 parts of potassium persulfate was added as a polymerization initiator, and to this were added 700 parts of styrene, 470 parts of butyl acrylate, and methacrylic l\J! 50 parts of mixed monomers were added dropwise into the flask continuously over a period of 3 hours. Thereafter, the reaction was further carried out at the same temperature for 2 hours to complete the polymerization. Furthermore, ammonia and dimethylethanolamine were added to pH 9.0.
And so.

得られたアクリル樹脂エマルジョンは、樹脂濃度60%
で、粘度s、oooセンチポイズ、T120℃であった
The obtained acrylic resin emulsion has a resin concentration of 60%.
The viscosity was s, ooo centipoise, and T120°C.

コノエマルションと水、メタノール、ブチルセロソルブ
を表1に示す割合で混合し、樹脂固形分が45%のスパ
ッターの付着防止剤を得た。この付着防止剤の性能は表
1のとおりであった。
Cono emulsion, water, methanol, and butyl cellosolve were mixed in the proportions shown in Table 1 to obtain a sputter adhesion inhibitor having a resin solid content of 45%. The performance of this anti-adhesion agent was as shown in Table 1.

実施例2〜6及び比較例1〜2 実施例1においてエマルジョンと水が表1の割合で、樹
脂固形分が異る以外は実施例1と同様にしてスパッター
の付着防止剤を得た。これらの性能は表1に示したとお
りであった。なお、園脂固形分が50%をこえる比較例
2の付着防止剤は粘度が高く、鋼板にうまく塗布するこ
とができなかったので、以後の試験は行わなかった。
Examples 2 to 6 and Comparative Examples 1 to 2 A sputter adhesion prevention agent was obtained in the same manner as in Example 1 except that the emulsion and water were in the proportions shown in Table 1 and the resin solid content was different. Their performance was as shown in Table 1. The anti-adhesion agent of Comparative Example 2, in which the solid content of resin exceeds 50%, had a high viscosity and could not be successfully applied to the steel plate, so further tests were not conducted.

&イ1)Hrq= vヤ9h+−3i刺馬7・為コ4比
鮫例1は発錆性、スパッター付着防止性が悪いが、本発
明の範囲内である実施例1〜6はいずれも性能が優れ、
特に実施例3〜5は優れているのがわかる。
&i1) Hrq=vya9h+-3iSashima7・Tameko4HisameExample 1 has poor rusting and spatter adhesion prevention properties, but Examples 1 to 6 which are within the scope of the present invention all have Excellent performance,
It can be seen that Examples 3 to 5 are particularly excellent.

実施例7〜11及び比較例3〜4 実施例3においてメタノールと水の割合が表2に示す以
外は実施例3と同様にしてスパッターの付着防止剤を得
た。性能は表2に示すとおりであった。
Examples 7 to 11 and Comparative Examples 3 to 4 Sputter adhesion inhibitors were obtained in the same manner as in Example 3, except that the ratios of methanol and water in Example 3 are shown in Table 2. The performance was as shown in Table 2.

表2よりメタノールが6%未満では乾燥性が悪くなり、
50%をこえると付着防止剤の安定性が悪くなることが
明らかである。
From Table 2, if methanol is less than 6%, drying performance becomes poor.
It is clear that when it exceeds 50%, the stability of the anti-adhesion agent deteriorates.

実施例12〜13 アルコールがメタノールのかわりに実施例12テはエタ
ノール、実施例16ではイソプロピルアルコールである
以外は実施例6と同様にして付着防止剤を得た。性能は
表〆のとおりであった。
Examples 12 to 13 An anti-adhesion agent was obtained in the same manner as in Example 6, except that the alcohol was ethanol in Example 12 and isopropyl alcohol in Example 16 instead of methanol. The performance was as shown in the table.

表  5 実施例14〜17 水及びモノマー組成が表4に示したとおりで、乳化剤が
ドデシルベンゼンスルホン酸ソーダである以外は実施例
1と同様にしてアクリル樹脂又はメタクリル樹脂エマル
ジョンを得た。樹脂固形分、T1は表4のとおりであっ
た。
Table 5 Examples 14 to 17 Acrylic resin or methacrylic resin emulsions were obtained in the same manner as in Example 1 except that the water and monomer compositions were as shown in Table 4 and the emulsifier was sodium dodecylbenzenesulfonate. The resin solid content and T1 were as shown in Table 4.

これらのアクリル樹脂エマルジョ/と水、メタノール、
ブチルセロソルブを表4に示す割合で混合しスパッター
の付着防止剤を得た。これらの性能は表4に示すとおり
で、いずれも良好であった。
These acrylic resin emulsion/water, methanol,
Butyl cellosolve was mixed in the proportions shown in Table 4 to obtain a sputter adhesion inhibitor. These performances are shown in Table 4, and all were good.

比較例5 樹脂固形分20%、粘度500センチボイズ、PH8,
0のポリアクリル酸アンモニウム塩50部、メタノール
10部、水40部を混合して、スパッター付着防止剤を
得た。
Comparative Example 5 Resin solid content 20%, viscosity 500 centivoise, PH8,
A sputter adhesion inhibitor was obtained by mixing 50 parts of polyacrylic acid ammonium salt of No. 0, 10 parts of methanol, and 40 parts of water.

性能等は次のとおりであった。Performance etc. were as follows.

粘度(センチボイズ)23 樹脂固形分開     10 乾燥性        良 塗膜平滑性      良 密着強度       80/100 耐水性         不良(完全に溶解)発錆性 
1昼夜後   やや有 7昼夜後   有 塗装性        70/100 スパツタ一付着防止性 12 (発明の効果) 以上より本発明のスパッター付着防止剤は防錆効果に優
れ、スパッターの付着は少くその意義は大きい。
Viscosity (centivoise) 23 Resin solid content 10 Drying property Good coating smoothness Good adhesion strength 80/100 Water resistance Poor (completely dissolved) Rust resistance
After 1 day and night Slightly Yes After 7 days and nights Paintability 70/100 Spatter adhesion prevention property 12 (Effect of the invention) From the above, the spatter adhesion preventive agent of the present invention has an excellent rust prevention effect and has little spatter adhesion, which is of great significance. .

Claims (1)

【特許請求の範囲】[Claims] 3〜50重量%の低級アルキルアルコールを含み、かつ
樹脂固形分が3〜50重量%である、水不溶性のアクリ
ル酸エステル又はメタクリル酸エステル重合体樹脂エマ
ルジョンよりなる溶接スパッターの付着防止剤。
A welding spatter adhesion inhibitor comprising a water-insoluble acrylic ester or methacrylic ester polymer resin emulsion containing 3 to 50% by weight of lower alkyl alcohol and having a resin solid content of 3 to 50% by weight.
JP25423184A 1984-12-03 1984-12-03 Adhesion preventing medium of welding spatter Pending JPS61132293A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP25423184A JPS61132293A (en) 1984-12-03 1984-12-03 Adhesion preventing medium of welding spatter

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP25423184A JPS61132293A (en) 1984-12-03 1984-12-03 Adhesion preventing medium of welding spatter

Publications (1)

Publication Number Publication Date
JPS61132293A true JPS61132293A (en) 1986-06-19

Family

ID=17262081

Family Applications (1)

Application Number Title Priority Date Filing Date
JP25423184A Pending JPS61132293A (en) 1984-12-03 1984-12-03 Adhesion preventing medium of welding spatter

Country Status (1)

Country Link
JP (1) JPS61132293A (en)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
AT402268B (en) * 1994-07-25 1997-03-25 Hoffmann Hans NON-STICK AGAINST WELDING SPLASH
US6811821B2 (en) 2001-03-30 2004-11-02 J & G Chemical Specialities, Llc Barrier coatings
CN103480986A (en) * 2013-09-22 2014-01-01 河南师范大学 Anti-splattering welding agent and preparation method thereof

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
AT402268B (en) * 1994-07-25 1997-03-25 Hoffmann Hans NON-STICK AGAINST WELDING SPLASH
US6811821B2 (en) 2001-03-30 2004-11-02 J & G Chemical Specialities, Llc Barrier coatings
CN103480986A (en) * 2013-09-22 2014-01-01 河南师范大学 Anti-splattering welding agent and preparation method thereof

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