JP4430387B2 - Cleaning agent before welding - Google Patents
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- JP4430387B2 JP4430387B2 JP2003409393A JP2003409393A JP4430387B2 JP 4430387 B2 JP4430387 B2 JP 4430387B2 JP 2003409393 A JP2003409393 A JP 2003409393A JP 2003409393 A JP2003409393 A JP 2003409393A JP 4430387 B2 JP4430387 B2 JP 4430387B2
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- 238000003466 welding Methods 0.000 title claims description 85
- 239000012459 cleaning agent Substances 0.000 title claims description 50
- 235000014113 dietary fatty acids Nutrition 0.000 claims description 28
- 229930195729 fatty acid Natural products 0.000 claims description 28
- 239000000194 fatty acid Substances 0.000 claims description 28
- 150000004665 fatty acids Chemical class 0.000 claims description 26
- -1 alicyclic amine Chemical class 0.000 claims description 25
- 239000007788 liquid Substances 0.000 claims description 21
- YNAVUWVOSKDBBP-UHFFFAOYSA-N Morpholine Chemical compound C1COCCN1 YNAVUWVOSKDBBP-UHFFFAOYSA-N 0.000 claims description 20
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 18
- 239000002736 nonionic surfactant Substances 0.000 claims description 17
- 239000002738 chelating agent Substances 0.000 claims description 15
- 150000003839 salts Chemical class 0.000 claims description 14
- 239000002518 antifoaming agent Substances 0.000 claims description 11
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 10
- OFOBLEOULBTSOW-UHFFFAOYSA-N Malonic acid Chemical compound OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 claims description 8
- 150000003333 secondary alcohols Chemical class 0.000 claims description 8
- KCXVZYZYPLLWCC-UHFFFAOYSA-N EDTA Chemical compound OC(=O)CN(CC(O)=O)CCN(CC(O)=O)CC(O)=O KCXVZYZYPLLWCC-UHFFFAOYSA-N 0.000 claims description 6
- QPCDCPDFJACHGM-UHFFFAOYSA-N N,N-bis{2-[bis(carboxymethyl)amino]ethyl}glycine Chemical compound OC(=O)CN(CC(O)=O)CCN(CC(=O)O)CCN(CC(O)=O)CC(O)=O QPCDCPDFJACHGM-UHFFFAOYSA-N 0.000 claims description 5
- 229920000570 polyether Polymers 0.000 claims description 5
- 239000004721 Polyphenylene oxide Substances 0.000 claims description 3
- 238000006386 neutralization reaction Methods 0.000 claims 2
- 238000004140 cleaning Methods 0.000 description 33
- 239000002184 metal Substances 0.000 description 18
- 229910052751 metal Inorganic materials 0.000 description 18
- 230000007547 defect Effects 0.000 description 14
- 239000000344 soap Substances 0.000 description 14
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 10
- 238000010894 electron beam technology Methods 0.000 description 8
- 239000003599 detergent Substances 0.000 description 7
- 230000000694 effects Effects 0.000 description 7
- 239000003921 oil Substances 0.000 description 7
- 150000001875 compounds Chemical class 0.000 description 5
- 229910052742 iron Inorganic materials 0.000 description 5
- JEIPFZHSYJVQDO-UHFFFAOYSA-N iron(III) oxide Inorganic materials O=[Fe]O[Fe]=O JEIPFZHSYJVQDO-UHFFFAOYSA-N 0.000 description 5
- 239000007921 spray Substances 0.000 description 5
- 239000000126 substance Substances 0.000 description 5
- 125000002091 cationic group Chemical group 0.000 description 4
- 239000003795 chemical substances by application Substances 0.000 description 4
- 230000001747 exhibiting effect Effects 0.000 description 4
- WWZKQHOCKIZLMA-UHFFFAOYSA-N octanoic acid Chemical compound CCCCCCCC(O)=O WWZKQHOCKIZLMA-UHFFFAOYSA-N 0.000 description 4
- 239000004071 soot Substances 0.000 description 4
- 239000002253 acid Substances 0.000 description 3
- 125000004432 carbon atom Chemical group C* 0.000 description 3
- 230000002950 deficient Effects 0.000 description 3
- 238000010790 dilution Methods 0.000 description 3
- 239000012895 dilution Substances 0.000 description 3
- 238000007654 immersion Methods 0.000 description 3
- 238000004519 manufacturing process Methods 0.000 description 3
- 238000002156 mixing Methods 0.000 description 3
- 238000004506 ultrasonic cleaning Methods 0.000 description 3
- HZAXFHJVJLSVMW-UHFFFAOYSA-N 2-Aminoethan-1-ol Chemical compound NCCO HZAXFHJVJLSVMW-UHFFFAOYSA-N 0.000 description 2
- HHPDFYDITNAMAM-UHFFFAOYSA-N 2-[cyclohexyl(2-hydroxyethyl)amino]ethanol Chemical compound OCCN(CCO)C1CCCCC1 HHPDFYDITNAMAM-UHFFFAOYSA-N 0.000 description 2
- 239000005635 Caprylic acid (CAS 124-07-2) Substances 0.000 description 2
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 description 2
- 229920002359 Tetronic® Polymers 0.000 description 2
- 150000001412 amines Chemical class 0.000 description 2
- PAFZNILMFXTMIY-UHFFFAOYSA-N cyclohexylamine Chemical compound NC1CCCCC1 PAFZNILMFXTMIY-UHFFFAOYSA-N 0.000 description 2
- ZBCBWPMODOFKDW-UHFFFAOYSA-N diethanolamine Chemical compound OCCNCCO ZBCBWPMODOFKDW-UHFFFAOYSA-N 0.000 description 2
- 238000004945 emulsification Methods 0.000 description 2
- 239000000839 emulsion Substances 0.000 description 2
- 230000002349 favourable effect Effects 0.000 description 2
- 239000007789 gas Substances 0.000 description 2
- 230000007257 malfunction Effects 0.000 description 2
- 229910021645 metal ion Inorganic materials 0.000 description 2
- 239000007769 metal material Substances 0.000 description 2
- 238000000034 method Methods 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- 229960002446 octanoic acid Drugs 0.000 description 2
- 125000004430 oxygen atom Chemical group O* 0.000 description 2
- 229920001983 poloxamer Polymers 0.000 description 2
- 239000000843 powder Substances 0.000 description 2
- 230000002265 prevention Effects 0.000 description 2
- 229910052710 silicon Inorganic materials 0.000 description 2
- 239000010703 silicon Substances 0.000 description 2
- 239000004094 surface-active agent Substances 0.000 description 2
- XZOYHFBNQHPJRQ-UHFFFAOYSA-N 7-methyloctanoic acid Chemical compound CC(C)CCCCCC(O)=O XZOYHFBNQHPJRQ-UHFFFAOYSA-N 0.000 description 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
- 241000519995 Stachys sylvatica Species 0.000 description 1
- 230000002159 abnormal effect Effects 0.000 description 1
- 239000012190 activator Substances 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 125000001931 aliphatic group Chemical group 0.000 description 1
- 238000002485 combustion reaction Methods 0.000 description 1
- 238000005520 cutting process Methods 0.000 description 1
- 230000007423 decrease Effects 0.000 description 1
- 238000005238 degreasing Methods 0.000 description 1
- 150000001991 dicarboxylic acids Chemical class 0.000 description 1
- 238000007865 diluting Methods 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 238000011156 evaluation Methods 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 238000011835 investigation Methods 0.000 description 1
- 230000001678 irradiating effect Effects 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 239000005416 organic matter Substances 0.000 description 1
- 229960003330 pentetic acid Drugs 0.000 description 1
- 229920001281 polyalkylene Polymers 0.000 description 1
- 229920000768 polyamine Polymers 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 229920002503 polyoxyethylene-polyoxypropylene Polymers 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 230000003449 preventive effect Effects 0.000 description 1
- 239000003566 sealing material Substances 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
Landscapes
- Detergent Compositions (AREA)
Description
本発明は、溶接前洗浄剤に関し、特に、電子ビーム溶接等の前処理において被溶接物表面に付着した有機物を洗浄、除去するのに好適な溶接前洗浄剤に関する。 The present invention relates to a pre-weld cleaning agent, and more particularly to a pre-weld cleaning agent suitable for cleaning and removing organic substances adhering to the surface of an object to be welded in a pretreatment such as electron beam welding.
金属部品の溶接には、電子ビーム溶接、レーザー溶接等の種々の溶接法が用いられる。例えば、電子ビーム溶接では、真空室の中で高速の電子ビームを金属部品に照射して溶接を行う。この際、被溶接物である金属部品の表面に加工油、乳化油等の有機物が付着していると、溶接時の熱により該有機物がガス化する。溶融状態の金属内部からガスが噴出することで、ブローホールやスパッタを生じる。このように、被溶接物の表面に付着した有機物は、溶接不良を引き起こす原因となる。そのため、溶接前には、被溶接物の表面を洗浄することが必要となる。 For welding metal parts, various welding methods such as electron beam welding and laser welding are used. For example, in electron beam welding, welding is performed by irradiating a metal part with a high-speed electron beam in a vacuum chamber. At this time, if an organic substance such as processing oil or emulsified oil adheres to the surface of the metal part to be welded, the organic substance is gasified by heat during welding. Blow holes and spatter are generated by gas jetting from inside the molten metal. Thus, the organic matter adhering to the surface of the workpiece is a cause of poor welding. Therefore, it is necessary to clean the surface of the workpiece before welding.
被溶接物の表面洗浄に用いる洗浄剤として、種々の成分のものが提案されている。例えば、特許文献1には、所定の構造を有する界面活性剤と、カチオン系油水分離剤であるポリアルキレンポリアミンジシアンアンモニウムクロライドとを含む水溶性洗浄剤が示されている。また、特許文献2には、少なくともモルホリン、ポリオキシエチレンポリオキシプロピレンブロックポリマー、炭素数6〜12の脂肪族酸、炭素数6〜18のジカルボン酸、水からなる洗浄剤が示されている。
上記特許文献1に示された水溶性洗浄剤は、カチオン系油水分離剤を配合し、洗浄液の油水分離性を向上させている。つまり、被洗浄物表面から加工油を除去するとともに、除去された加工油と界面活性剤とが結合したエマルジョンを洗浄液から分離、除去し易くし、エマルジョンの被洗浄物への再付着を抑制している。 The water-soluble cleaning agent disclosed in Patent Document 1 contains a cationic oil / water separating agent to improve the oil / water separating property of the cleaning liquid. In other words, the processing oil is removed from the surface of the object to be cleaned, and the emulsion in which the removed processing oil and the surfactant are combined is easily separated and removed from the cleaning liquid, and the reattachment of the emulsion to the object to be cleaned is suppressed. ing.
しかし、カチオン系油水分離剤は、被洗浄物である金属材料に吸着し易いため、洗浄後に被洗浄物の表面に残留し易い。残留したカチオン系油水分離剤は、溶接時の熱によりガス化して、ブローホールやスパッタの原因となる。また、燃焼後に煤やヤニ等の燃えかすが残り、それにより溶接不良が引き起こされるおそれもある。 However, since the cationic oil-water separator is easily adsorbed on the metal material that is the object to be cleaned, it tends to remain on the surface of the object to be cleaned after cleaning. The remaining cationic oil-water separating agent is gasified by heat during welding and causes blowholes and spatter. In addition, there is a risk that soot and spear remain after combustion, which may cause poor welding.
電子ビーム溶接の際にスパッタが発生すると、それにより真空室のシール材が劣化して空気漏れが生じる。真空度が低下すると、アーキング(異常放電)を招くおそれがある。加えて、溶接時に煤等が生じると、真空ポンプが汚染され不具合を生じる。 If spatter occurs during electron beam welding, the sealing material in the vacuum chamber deteriorates and air leakage occurs. When the degree of vacuum decreases, there is a risk of causing arcing (abnormal discharge). In addition, if flaws or the like are generated during welding, the vacuum pump is contaminated and causes a malfunction.
また、上記特許文献2に示された洗浄剤は、アミンとしてモルホリンを含む。遊離アミンがモルホリンのみとなるため、臭気がひどく、実用性に乏しい。また、同洗浄剤に含まれる粉末状のジカルボン酸は、モルホリンとの結合力が弱いため、洗浄後の乾燥によりもとの粉末に戻ってしまう。そのため、被洗浄物表面には白いシミが残り、溶接不良を引き起こす。 Moreover, the cleaning agent disclosed in Patent Document 2 contains morpholine as an amine. Since the free amine is only morpholine, it has a bad odor and is not practical. Moreover, since the powdery dicarboxylic acid contained in the detergent has a weak binding force with morpholine, it returns to the original powder by drying after washing. For this reason, white spots remain on the surface of the object to be cleaned, causing poor welding.
このように、洗浄剤の成分により、溶接不良や溶接装置の不具合が引き起こされる場合がある。したがって、溶接前の洗浄に使用する洗浄剤は、溶接不良等の原因となり得る成分をできるだけ含まないことが望ましい。換言すれば、該洗浄剤を、溶接性を阻害し難い成分で構成することが望ましい。 As described above, the components of the cleaning agent may cause poor welding or defects in the welding apparatus. Therefore, it is desirable that the cleaning agent used for cleaning before welding does not contain as much components as possible that may cause welding defects. In other words, it is desirable that the cleaning agent is composed of a component that is difficult to inhibit weldability.
さらに、被洗浄物の表面には、金属石鹸が付着していることが多い。金属石鹸は、金属イオンと脂肪酸との化合物である。金属石鹸は、被洗浄物の切削加工時に用いられる加工油剤に含まれることが多く、それが被洗浄物の表面に付着する。また、水中の金属イオンと洗浄剤中の脂肪酸とから生成される場合もある。本発明者が、溶接時に生成したブローホール内部の気体成分を分析した結果、その約90%は水素であることがわかった。これより、ブローホールの多くは、被洗浄物の表面に付着した金属石鹸が、溶接時にガス化することで生成されると考えられる。したがって、被洗浄物の表面に金属石鹸が付着している場合には、その金属石鹸を除去することが重要となる。しかし、上記特許文献1、2に示された洗浄剤を含めて、従来の水溶性洗浄剤では、被洗浄物の表面に付着した金属石鹸を充分に除去することはできない。 Further, metal soap often adheres to the surface of the object to be cleaned. Metal soap is a compound of metal ions and fatty acids. Metal soap is often contained in a processing oil used when cutting an object to be cleaned, and adheres to the surface of the object to be cleaned. Moreover, it may be produced | generated from the metal ion in water and the fatty acid in a cleaning agent. As a result of analysis of the gas component inside the blowhole generated by the inventor by the present inventor, it was found that about 90% is hydrogen. From this, it is considered that many blow holes are generated by gasifying the metal soap attached to the surface of the object to be cleaned during welding. Therefore, when metal soap adheres to the surface of the object to be cleaned, it is important to remove the metal soap. However, the conventional water-soluble cleaning agents including the cleaning agents disclosed in Patent Documents 1 and 2 cannot sufficiently remove the metal soap adhered to the surface of the object to be cleaned.
本発明は、このような実状に鑑みてなされたものであり、溶接前の洗浄に使用しても、溶接不良や溶接装置の不具合を引き起こし難い溶接前洗浄剤を提供することを課題とする。加えて、被洗浄物の表面に付着した金属石鹸をも除去することのできる溶接前洗浄剤を提供することを課題とする。 The present invention has been made in view of such a situation, and it is an object of the present invention to provide a pre-welding cleaning agent that is unlikely to cause welding failure or failure of a welding apparatus even when used for cleaning before welding . In addition, it is an object of the present invention to provide a pre-welding cleaning agent that can also remove metal soap adhered to the surface of an object to be cleaned.
本発明の溶接前洗浄剤は、モルホリンを含む脂環式アミン1〜40wt%と、液状脂肪酸1〜20wt%と、非イオン界面活性剤1〜5wt%と、水残部とを主剤とし、粉末状のジカルボン酸を含まないことを特徴とする。本発明の溶接前洗浄剤は、洗浄成分として非イオン界面活性剤を含み、被洗浄物表面の有機物を効果的に除去する。また、脂環式アミンと液状脂肪酸とを含むため、被洗浄物表面の錆止め作用をも有する。すなわち、本発明の溶接前洗浄剤で洗浄すると、脂環式アミンと液状脂肪酸との中和塩からなる皮膜が被洗浄物の表面に形成される。その結果、被洗浄物表面における錆の発生が効果的に抑制される。 The pre-weld cleaning agent of the present invention is mainly composed of 1 to 40 wt% of alicyclic amine containing morpholine, 1 to 20 wt% of liquid fatty acid, 1 to 5 wt% of nonionic surfactant, and the remainder of water, and is in powder form It is characterized by not containing any dicarboxylic acid . The pre-welding cleaning agent of the present invention contains a nonionic surfactant as a cleaning component, and effectively removes organic substances on the surface of the object to be cleaned. Moreover, since it contains an alicyclic amine and a liquid fatty acid, it also has a rust preventive action on the surface of the object to be cleaned. That is, when washed with the pre-welding detergent of the present invention, a film made of a neutralized salt of an alicyclic amine and a liquid fatty acid is formed on the surface of the object to be cleaned. As a result, generation of rust on the surface of the object to be cleaned is effectively suppressed.
本発明者は、脂環式アミンおよび液状脂肪酸について、溶接時の燃えかす(煤、ヤニ)生成の有無、および燃焼性を調査した。燃焼性は、被洗浄物となる金属材料の一例として鉄を想定し、鉄が溶融する前にガス化し易いかどうかを調べた。鉄の溶融前にガス化して無くなれば、ブローホールやスパッタの原因となり難いといえる。調査結果を、通常、洗浄剤に用いられる他の化合物と比較して、下記表1、表2に示す。各表中の燃焼性を示す記号は、試料に着火した後に火種を遠ざけた場合、◎:燃焼し続け最後まで燃え切る、○:燃焼し続けるが燃え残りが有る、△:しばらくして火が消え燃え残りが多い、×:すぐに火が消え燃え残りが多い、を示す。また、総合判断を示す記号は、◎:好適、○:適、×:不適、を示す。 This inventor investigated the presence or absence of flaming (soot, spear) production | generation at the time of welding, and combustibility about alicyclic amine and liquid fatty acid. As for the combustibility, iron was assumed as an example of a metal material to be cleaned, and it was examined whether or not it was easily gasified before the iron melted. If it is not gasified before melting of iron, it can be said that it is difficult to cause blowholes and spatter. The investigation results are shown in Tables 1 and 2 below in comparison with other compounds usually used in cleaning agents. Symbols indicating flammability in each table indicate that when the sample is ignited and the fire type is moved away, ◎: Continue to burn and burn to the end, ○: Continue to burn but have unburned, △: Fire after a while Excessive burn-out remaining, x: Indicates that the fire is extinguished immediately and there is much unburned residue. In addition, symbols indicating comprehensive judgment indicate ◎: suitable, ○: suitable, ×: inappropriate.
表1に示すように、脂環式アミンでは、エタノールアミン等と比較して、ヤニの生成が無く、燃焼性も良好であった。また、表2に示すように、液状脂肪酸でも、粉末状のジカルボン酸と比較して、煤およびヤニの生成が少なく、燃焼性も良好であった。つまり、脂環式アミンおよび液状脂肪酸は、洗浄後に被洗浄物の表面に残存しても、溶接不良等を引き起こし難いといえる。これに対して粉末状のジカルボン酸は、燃えかすが多く、燃焼性も悪いので、被洗浄物の表面に残存すると溶接不良等を引き起こす原因となる。 As shown in Table 1, in the alicyclic amine, there was no generation | occurrence | production of a spear and favorable combustibility compared with ethanolamine etc. Further, as shown in Table 2, even in the case of liquid fatty acids, generation of soot and spears was small and combustibility was good as compared with powdered dicarboxylic acids . That is, it can be said that even if the alicyclic amine and the liquid fatty acid remain on the surface of the object to be cleaned after cleaning, it is difficult to cause poor welding or the like. On the other hand, powdered dicarboxylic acid often burns and has poor flammability, and if it remains on the surface of the object to be cleaned, it causes a welding failure or the like.
したがって、脂環式アミンと液状脂肪酸とを含み、粉末状のジカルボン酸を含まない本発明の溶接前洗浄剤を用いて洗浄すれば、その後の溶接において、溶接不良や溶接装置の不具合の発生を低減することができる。 Therefore, if cleaning is performed using the pre-welding cleaning agent of the present invention that contains an alicyclic amine and a liquid fatty acid and does not contain a powdered dicarboxylic acid , in the subsequent welding, welding defects or defects in the welding apparatus may occur. Can be reduced.
本発明の溶接前洗浄剤は、上記主剤に加え、さらにキレート剤を含んで構成すると好適である。上述したように、被洗浄物の表面には、金属石鹸が付着していることが多い。キレート剤を配合することで、金属石鹸を錯化合物として効果的に除去することができる。したがって、キレート剤を含む態様の本発明の溶接前洗浄剤を用いて洗浄すれば、溶接不良や溶接装置の不具合の発生をより低減することができる。 The pre-welding cleaning agent of the present invention preferably contains a chelating agent in addition to the main agent. As described above, metal soap is often attached to the surface of the object to be cleaned. By blending the chelating agent, the metal soap can be effectively removed as a complex compound. Therefore, if it wash | cleans using the cleaning agent before welding of this invention of the aspect containing a chelating agent, generation | occurrence | production of the welding defect and the malfunction of a welding apparatus can be reduced more.
本発明の溶接前洗浄剤は、脂環式アミンと、液状脂肪酸と、非イオン界面活性剤とを主剤とし、粉末状のジカルボン酸を含まない。本発明の溶接前洗浄剤は、溶接性を阻害し難い成分で構成されるため、溶接前の洗浄に使用しても、溶接不良や溶接装置の不具合を引き起こし難い。また、さらにキレート剤を配合することにより、被洗浄物表面に付着した金属石鹸を効果的に除去することができる。その結果、洗浄後の溶接における溶接不良や溶接装置の不具合の発生を、より抑制することができる。 The pre-welding cleaning agent of the present invention mainly comprises an alicyclic amine, a liquid fatty acid, and a nonionic surfactant, and does not contain a powdered dicarboxylic acid . Since the pre-weld cleaning agent of the present invention is composed of components that do not easily impair weldability, even when used for cleaning before welding, it is difficult to cause poor welding or problems with the welding apparatus. Moreover, the metal soap adhering to the to-be-washed | cleaned object surface can be effectively removed by mix | blending a chelating agent further. As a result, it is possible to further suppress the occurrence of defective welding and defects in the welding apparatus in the weld after cleaning.
以下、本発明の溶接前洗浄剤について詳細に説明する。なお、本発明の溶接前洗浄剤は、下記の実施形態に限定されるものではない。本発明の溶接前洗浄剤は、本発明の要旨を逸脱しない範囲において、当業者が行い得る変更、改良等を施した種々の形態にて実施することができる。 Hereinafter, the pre-welding detergent of the present invention will be described in detail. In addition, the cleaning agent before welding of this invention is not limited to the following embodiment. The pre-welding cleaning agent of the present invention can be implemented in various forms that have been modified or improved by those skilled in the art without departing from the scope of the present invention.
本発明の溶接前洗浄剤は、脂環式アミンと、液状脂肪酸と、非イオン界面活性剤とを主剤とし、粉末状のジカルボン酸を含まずに構成される。脂環式アミンは、水溶性のものであるとよい。脂環式アミンは、モルホリンを含み、その他の脂環式アミンを含んでもよい。その他の脂環式アミンは、水溶性のものであればその種類が特に限定されるものではなく、例えば、N−シクロヘキシルジエタノールアミン、シクロヘキシルアミン等が挙げられる。これら脂環式アミンの一種を単独で、また二種以上を混合して用いればよい。なかでも、分子内に酸素原子を含む化合物は、鉄が溶融する前にガス化し易く、燃焼性が良好であるため好適である。特に、モルホリンのように、環の中に酸素原子を含む化合物を用いるとよい。この場合、モルホリンは液状脂肪酸との中和塩として存在するため、上述した臭気の問題はない。 The pre-welding cleaning agent of the present invention is composed mainly of an alicyclic amine, a liquid fatty acid, and a nonionic surfactant and does not contain a powdered dicarboxylic acid . The alicyclic amine is preferably water-soluble. The alicyclic amine contains morpholine and may contain other alicyclic amines. The type of other alicyclic amine is not particularly limited as long as it is water-soluble, and examples thereof include N-cyclohexyldiethanolamine and cyclohexylamine. These alicyclic amines may be used alone or in combination of two or more. Especially, the compound which contains an oxygen atom in a molecule | numerator is suitable since it is easy to gasify before iron melt | dissolves and combustibility is favorable. In particular, a compound containing an oxygen atom in the ring, such as morpholine, may be used. In this case, since morpholine exists as a neutralized salt with liquid fatty acid, there is no problem of odor described above.
本発明の溶接前洗浄剤における脂環式アミンの含有割合は、1〜40wt%である。防錆効果を効果的に発揮させるという観点から、脂環式アミンの含有割合を1wt%以上とする。防錆効果を高くしたい場合には、脂環式アミンの含有割合を高くすればよい。しかし、コスト等の実用性を考慮すれば、脂環式アミンの含有割合を40wt%以下とする。特に、溶接不良等をより少なくするという観点からは、25wt%以下とすることが望ましい。10wt%以下とするとより好適である。 The content rate of the alicyclic amine in the cleaning agent before welding of this invention is 1-40 wt%. From the viewpoint of effectively exhibiting the anticorrosive effect, the content of the alicyclic amine shall be the 1 wt% or more. In order to increase the rust prevention effect, the content of the alicyclic amine may be increased. However, considering practicality such as cost, the content of the alicyclic amine is set to 40 wt% or less . In particular, from the viewpoint of reducing welding defects and the like, it is desirable that the content be 25 wt% or less. More preferably, it is 10 wt% or less.
なお、本明細書では、本発明の溶接前洗浄剤を水で1%以上3%以下の濃度に希釈して使用することを前提として、各成分の好適な含有割合を示す。したがって、使用する際の希釈率が上記範囲と異なる場合には、希釈率に応じて、各成分の含有割合を適宜調整すればよい。 In addition, in this specification, the suitable content rate of each component is shown on the assumption that the cleaning agent before welding of the present invention is diluted with water to a concentration of 1% or more and 3% or less. Therefore, when the dilution rate at the time of use differs from the said range, what is necessary is just to adjust the content rate of each component suitably according to a dilution rate.
液状脂肪酸の種類は、特に限定されるものではない。例えば、炭素数が9以下のカプリル酸、イソノナン酸等が挙げられる。これら液状脂肪酸の一種を単独で、また二種以上を混合して用いればよい。 The type of liquid fatty acid is not particularly limited. Examples thereof include caprylic acid having 9 or less carbon atoms and isononanoic acid. These liquid fatty acids may be used alone or in combination of two or more.
本発明の溶接前洗浄剤における液状脂肪酸の含有割合は、1〜20wt%とする。防錆効果を効果的に発揮させるという観点から、液状脂肪酸の含有割合を1wt%以上とする。一方、コストなどの実用性を考慮すれば、液状脂肪酸の含有割合を20wt%以下とする。特に、溶接不良等をより少なくするという観点からは、10wt%以下とすることが望ましい。5wt%以下とするとより好適である。 The content rate of the liquid fatty acid in the cleaning agent before welding of this invention shall be 1-20 wt%. From the viewpoint of effectively exhibiting the rust prevention effect, the content ratio of the liquid fatty acid is 1 wt% or more . On the other hand, in consideration of practicality such as cost, the content ratio of the liquid fatty acid is set to 20 wt% or less . In particular, from the viewpoint of reducing welding defects and the like, it is desirable that the content be 10 wt% or less. More preferably, it is 5 wt% or less.
非イオン系界面活性剤は、既に公知の活性剤を用いればよい。例えば、高級アルコールエトキシレート、プルロニックタイプ、テトロニックタイプ、脂肪族アミンエトキシレート、ソルビタン脂肪酸エステルエトキシレート、脂肪酸ポリエーテル、セカンダリアルコールエトキシレート等が挙げられる。これら非イオン系界面活性剤の一種を単独で、また二種以上を混合して用いればよい。 As the nonionic surfactant, a known activator may be used. Examples include higher alcohol ethoxylates, pluronic types, tetronic types, aliphatic amine ethoxylates, sorbitan fatty acid ester ethoxylates, fatty acid polyethers, secondary alcohol ethoxylates, and the like. One kind of these nonionic surfactants may be used alone, or two or more kinds may be mixed and used.
本発明者は、各種非イオン系界面活性剤について、上記環式アミン等と同様に、溶接時の燃えかす(煤、ヤニ)生成の有無、および燃焼性を調査した。調査結果を表3に示す。なお、各表中の総合判断における記号は、◎:好適、○:適、△:やや問題有りを示す。 The present inventor investigated the presence or absence of flaming (soot, spear) generation and flammability of various nonionic surfactants in the same manner as the cyclic amines described above. The survey results are shown in Table 3. In addition, the symbol in the comprehensive judgment in each table | surface shows (double-circle): suitable, (circle): suitable, (triangle | delta): Somewhat problematic.
表3に示すように、高級アルコールエトキシレートおよび脂肪酸ポリエーテルでは、燃えかすがほとんどなく、燃焼性も良好であった。これより、両者は溶接性の観点では好適であることがわかる。また、プルロニックタイプ、テトロニックタイプ、およびセカンダリアルコールエトキシレートでは、ヤニの生成が少々有り、高級アルコールエトキシレートおよび脂肪酸ポリエーテルより燃焼性が劣る結果となった。なお、セカンダリアルコールエトキシレートを用いると、乳化特性が向上し、化学的な脱脂性能を向上させることができる。このため、スプレー洗浄以外の、物理的な洗浄力の乏しい超音波洗浄や浸漬洗浄を行う場合には、セカンダリアルコールエトキシレートを用いるとよい。 As shown in Table 3, the higher alcohol ethoxylate and the fatty acid polyether had almost no burnout and good combustibility. This shows that both are suitable from the viewpoint of weldability. In addition, the Pluronic type, Tetronic type, and secondary alcohol ethoxylate produced a small amount of spear, resulting in inferior combustibility compared with higher alcohol ethoxylate and fatty acid polyether. In addition, when a secondary alcohol ethoxylate is used, an emulsification characteristic will improve and chemical degreasing performance can be improved. For this reason, when performing ultrasonic cleaning or immersion cleaning with poor physical cleaning power other than spray cleaning, secondary alcohol ethoxylate may be used.
一方、脂肪族アミンエトキシレートおよびソルビタン脂肪酸エステルエトキシレートでは、燃えかすが少々残り、燃焼性は良好ではなかった。そのため、溶接性の観点では、やや問題有りという結果となった。以上より、非イオン界面活性剤は、高級アルコールエトキシレート、脂肪酸ポリエーテル、セカンダリアルコールエトキシレートから選ばれる一種以上を含む態様が望ましいといえる。 On the other hand, with the aliphatic amine ethoxylate and sorbitan fatty acid ester ethoxylate, a slight amount of burnt residue remained, and the flammability was not good. For this reason, there was a slight problem in terms of weldability. From the above, it can be said that the nonionic surfactant preferably includes at least one selected from higher alcohol ethoxylates, fatty acid polyethers, and secondary alcohol ethoxylates.
本発明の溶接前洗浄剤における非イオン界面活性剤の含有割合は、1〜5wt%とする。実用上の洗浄効果を発揮させるという観点から、非イオン界面活性剤の含有割合を1wt%以上とする。一方、コスト等の実用性を考慮すれば、物理的な洗浄力に長けたスプレー洗浄等の場合、非イオン界面活性剤の含有割合を5wt%以下とする。特に、3wt%程度が好適である。 The content ratio of the nonionic surfactant in the pre-welding detergent of the present invention is 1 to 5 wt%. From the viewpoint of exhibiting the cleaning effect of the practical, the content of the nonionic surfactant shall be the 1 wt% or more. On the other hand, if practicality such as cost is taken into consideration, the content ratio of the nonionic surfactant is set to 5 wt% or less in the case of spray cleaning or the like with excellent physical cleaning power . In particular, about 3 wt% is preferable.
本発明の溶接前洗浄剤は、上記主剤に加え、さらにキレート剤を含んで構成すると好適である。この場合、被洗浄物の表面に付着した金属石鹸を、効果的に除去することができる。使用するキレート剤の種類は、特に限定されるものではない。例えば、EDTA(エチレンジアミン四酢酸)無機中和塩、EDTA有機中和塩、DTPA(ジエチレントリアミン五酢酸)無機中和塩、DTPA有機中和塩、ポリカルボン酸無機中和塩、ポリカルボン酸有機中和塩等が挙げられる。これらキレート剤の一種を単独で、また二種以上を混合して用いればよい。なかでも、EDTA有機中和塩およびDTPA有機中和塩は、他のものと比べて燃えかすが少なく、燃焼性が良好であるため好適である。 The pre-welding cleaning agent of the present invention preferably contains a chelating agent in addition to the main agent. In this case, the metal soap adhering to the surface of the object to be cleaned can be effectively removed. The kind of chelating agent to be used is not particularly limited. For example, EDTA (ethylenediaminetetraacetic acid) inorganic neutralized salt, EDTA organic neutralized salt, DTPA (diethylenetriaminepentaacetic acid) inorganic neutralized salt, DTPA organic neutralized salt, polycarboxylic acid inorganic neutralized salt, polycarboxylic acid organic neutralized salt Examples include salts. One kind of these chelating agents may be used alone, or two or more kinds may be mixed and used. Among these, the EDTA organic neutralized salt and the DTPA organic neutralized salt are preferable because they are less combustible than other materials and have good combustibility.
本発明の溶接前洗浄剤におけるキレート剤の含有割合は、特に限定されるものではない。金属石鹸の除去効果を効果的に発揮させるという観点から、キレート剤の含有割合を1wt%以上とすることが望ましい。一方、コスト等の実用性を考慮すれば、キレート剤の含有割合を20wt%以下とすることが望ましい。特に、溶接不良等をより少なくするという観点からは、10wt%以下とすることが望ましい。5wt%以下とするとより好適である。 The content ratio of the chelating agent in the pre-welding detergent of the present invention is not particularly limited. From the viewpoint of effectively exhibiting the effect of removing the metal soap, the content of the chelating agent is preferably 1 wt% or more. On the other hand, in view of practicality such as cost, it is desirable that the content of the chelating agent is 20 wt% or less. In particular, from the viewpoint of reducing welding defects and the like, it is desirable that the content be 10 wt% or less. More preferably, it is 5 wt% or less.
また、本発明の溶接前洗浄剤は、必要に応じて上記以外の種々の添加剤を含めることができる。例えば、消泡剤等を含めることができる。ここで、消泡剤には、シリコン系消泡剤、アルコール系消泡剤等が挙げられる。しかし、シリコン系消泡剤の燃焼性は悪く、溶接時には燃えかすが多く残存する。そのため、溶接性を考慮した場合には、燃えかすが残らず、かつ燃焼性が良好なアルコール系消泡剤を用いることが望ましい。消泡剤を添加する場合、その含有割合は特に限定されるものではない。消泡効果を発揮させるには、1wt%以下で充分である。0.5wt%程度とすると好適である。 Moreover, the cleaning agent before welding of this invention can contain various additives other than the above as needed. For example, an antifoaming agent etc. can be included. Here, examples of the antifoaming agent include a silicon-based antifoaming agent and an alcohol-based antifoaming agent. However, the flammability of the silicon-based antifoaming agent is poor, and many burnouts remain during welding. Therefore, in consideration of weldability, it is desirable to use an alcohol-based antifoaming agent that does not leave flaming and has good flammability. When adding an antifoamer, the content rate is not specifically limited. In order to exhibit the defoaming effect, 1 wt% or less is sufficient. About 0.5 wt% is preferable.
本発明の溶接前洗浄剤は、上記所定の成分と、溶媒である水とを混合して調製される。そして、必要に応じて水で希釈して使用する。希釈率は、所望の効果が得られる範囲で適宜設定することができる。例えば、本発明の溶接前洗浄剤を水で1%以上3%以下の濃度に希釈して使用すればよい。本発明の溶接前洗浄剤は、スプレー洗浄、超音波洗浄、浸漬洗浄等、種々の洗浄方法に用いることができる。また、本発明の溶接前洗浄剤は、電子ビーム溶接、レーザー溶接等の種々の溶接の前洗浄に好適である。 The pre-welding cleaning agent of the present invention is prepared by mixing the predetermined component and water as a solvent. And it dilutes with water as needed and uses it. The dilution rate can be appropriately set as long as a desired effect is obtained. For example, the pre-weld cleaning agent of the present invention may be used after diluting with water to a concentration of 1% or more and 3% or less. The pre-welding cleaner of the present invention can be used in various cleaning methods such as spray cleaning, ultrasonic cleaning, and immersion cleaning. Further, the pre-weld cleaning agent of the present invention is suitable for pre-cleaning of various weldings such as electron beam welding and laser welding.
以下、本発明の溶接前洗浄剤の好適な態様を示す。
(1)脂環式アミン :1wt%以上5wt%以下
液状脂肪酸 :1wt%以上5wt%以下
非イオン界面活性剤:1wt%以上5wt%以下
キレート剤 :1wt%以上5wt%以下
消泡剤 :1wt%以下
水 :残部
本態様では、被洗浄物表面に付着した金属石鹸を効果的に除去することができ、洗浄後の溶接においても、溶接不良や溶接装置の不具合の発生を抑制することができる。
(2)脂環式アミン :10wt%以上20wt%以下
液状脂肪酸 :3wt%以上5wt%以下
非イオン界面活性剤:3wt%以上5wt%以下
キレート剤 :1wt%以上5wt%以下
消泡剤 :1wt%以下
水 :残部
本態様は、脂環式アミンの含有割合が高いため、洗浄後の部品における錆の発生をより抑制したい場合に好適である。
(3)脂環式アミン :1wt%以上5wt%以下
液状脂肪酸 :1wt%以上5wt%以下
非イオン界面活性剤(セカンダリアルコールエトキシレート)
:10wt%以上15wt%以下
キレート剤 :1wt%以上5wt%以下
消泡剤 :1wt%以下
水 :残部
本態様では、非イオン界面活性剤として乳化特性に優れるセカンダリアルコールエトキシレートを使用している。よって、物理的な洗浄力に乏しい超音波洗浄や浸漬洗浄を行う場合に好適である。
Hereinafter, the suitable aspect of the cleaning agent before welding of this invention is shown.
(1) Alicyclic amine: 1 wt% to 5 wt% Liquid fatty acid: 1 wt% to 5 wt% Nonionic surfactant: 1 wt% to 5 wt% Chelating agent: 1 wt% to 5 wt% Antifoam: 1 wt% Hereinafter, water: remainder In this embodiment, the metal soap adhering to the surface of the object to be cleaned can be effectively removed, and it is possible to suppress the occurrence of poor welding and defects in the welding apparatus even in welding after cleaning.
(2) Alicyclic amine: 10 wt% to 20 wt% Liquid fatty acid: 3 wt% to 5 wt% Nonionic surfactant: 3 wt% to 5 wt% Chelating agent: 1 wt% to 5 wt% Antifoam: 1 wt% Hereinafter, water: balance This embodiment is suitable when the content of alicyclic amine is high and it is desirable to further suppress the occurrence of rust in the cleaned parts.
(3) Alicyclic amine: 1 wt% or more and 5 wt% or less Liquid fatty acid: 1 wt% or more and 5 wt% or less Nonionic surfactant (secondary alcohol ethoxylate)
: 10 wt% or more and 15 wt% or less Chelating agent: 1 wt% or more and 5 wt% or less Antifoaming agent: 1 wt% or less Water: Remaining In this aspect, the secondary alcohol ethoxylate which is excellent in an emulsification characteristic is used as a nonionic surfactant. Therefore, it is suitable when performing ultrasonic cleaning and immersion cleaning with poor physical cleaning power.
上記実施形態に基づいて、本発明の溶接前洗浄剤を調製した。調製した溶接前洗浄剤を用いて、電子ビーム溶接の前洗浄を行い、その後の溶接における溶接不良および溶接装置の不具合の発生を調査した。以下、順に説明する。 Based on the said embodiment, the cleaning agent before welding of this invention was prepared. Using the prepared pre-weld cleaning agent, pre- cleaning of electron beam welding was performed, and the occurrence of welding defects and defects in the welding apparatus in subsequent welding was investigated. Hereinafter, it demonstrates in order.
(1)溶接前洗浄剤の調製
以下の組成および含有割合の溶接前洗浄剤を調製した。
N−シクロヘキシルジエタノールアミン:2.5wt%
モルホリン :2.5wt%
カプリル酸 :3wt%
高級アルコールエトキシレート :3wt%
EDTA有機中和塩 :3wt%
アルコール系消泡剤 :0.5wt%
水 :残部
(2)洗浄
上記溶接前洗浄剤を、水で約1%の濃度に希釈し、希釈洗浄剤とした。この希釈洗浄剤を使用して、スプレー洗浄装置にて、鉄製のデフケースを洗浄した。洗浄条件は、希釈洗浄剤温度60〜80℃、スプレー圧力0.3MPa、洗浄時間25秒とした。
(1) was prepared before welding detergent composition and content of the following preparation of pre-weld cleaning agent.
N-cyclohexyldiethanolamine: 2.5 wt%
Morpholine: 2.5 wt%
Caprylic acid: 3wt%
Higher alcohol ethoxylate: 3wt%
EDTA organic neutralized salt: 3wt%
Alcohol-based antifoaming agent: 0.5 wt%
Water: remainder (2) Cleaning The pre-welding cleaning agent was diluted with water to a concentration of about 1% to obtain a diluted cleaning agent. Using this diluted cleaning agent, the iron differential case was cleaned with a spray cleaning device. The cleaning conditions were a diluted cleaning agent temperature of 60 to 80 ° C., a spray pressure of 0.3 MPa, and a cleaning time of 25 seconds.
(3)溶接性の評価
上記洗浄後のデフケースを電子ビーム溶接し、ブローホールの発生等による溶接不良品の発生率、および溶接装置の故障頻度を調査した。その結果、従来の洗浄剤(商品名「ケミーライトCP−60MK(T)」、島田化成株式会社製)で洗浄した場合と比較して、溶接不良品の発生率は半減した。また、溶接装置の故障頻度は60%以上低減した。
(3) Evaluation of weldability The differential case after the cleaning was electron beam welded, and the occurrence rate of defective welds due to the occurrence of blowholes and the failure frequency of the welding apparatus were investigated. As a result, the incidence of defective welds was reduced by half compared to the case of cleaning with a conventional cleaning agent (trade name “Chemite Light CP-60MK (T)”, manufactured by Shimada Kasei Co., Ltd.). Moreover, the failure frequency of the welding apparatus was reduced by 60% or more.
以上より、本発明の溶接前洗浄剤を用いて洗浄することにより、その後の溶接における溶接不良や溶接装置の不具合の発生を低減できることが確認された。 From the above, it has been confirmed that by using the pre-weld cleaning agent of the present invention for cleaning, it is possible to reduce the occurrence of welding defects and defects in the welding apparatus in subsequent welding.
Claims (5)
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2003409393A JP4430387B2 (en) | 2003-12-08 | 2003-12-08 | Cleaning agent before welding |
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