JPS5855832B2 - How to cover the side seams of welded cans - Google Patents
How to cover the side seams of welded cansInfo
- Publication number
- JPS5855832B2 JPS5855832B2 JP5440678A JP5440678A JPS5855832B2 JP S5855832 B2 JPS5855832 B2 JP S5855832B2 JP 5440678 A JP5440678 A JP 5440678A JP 5440678 A JP5440678 A JP 5440678A JP S5855832 B2 JPS5855832 B2 JP S5855832B2
- Authority
- JP
- Japan
- Prior art keywords
- resin
- paint
- coating
- film
- slurry paint
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired
Links
- 238000000576 coating method Methods 0.000 claims description 60
- 239000011248 coating agent Substances 0.000 claims description 55
- 239000003973 paint Substances 0.000 claims description 46
- 239000002002 slurry Substances 0.000 claims description 29
- 229920005989 resin Polymers 0.000 claims description 17
- 239000011347 resin Substances 0.000 claims description 17
- 238000000034 method Methods 0.000 claims description 15
- 239000000126 substance Substances 0.000 claims description 8
- 238000002844 melting Methods 0.000 claims description 7
- 230000008018 melting Effects 0.000 claims description 7
- 239000000463 material Substances 0.000 claims description 6
- 239000003822 epoxy resin Substances 0.000 claims description 4
- 229920000647 polyepoxide Polymers 0.000 claims description 4
- 239000005011 phenolic resin Substances 0.000 claims description 3
- 229920006230 thermoplastic polyester resin Polymers 0.000 claims description 3
- 229920000178 Acrylic resin Polymers 0.000 claims description 2
- 239000004925 Acrylic resin Substances 0.000 claims description 2
- 239000004593 Epoxy Substances 0.000 claims description 2
- 239000004721 Polyphenylene oxide Substances 0.000 claims description 2
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 claims description 2
- 229920000180 alkyd Polymers 0.000 claims description 2
- 229920003180 amino resin Polymers 0.000 claims description 2
- 150000002148 esters Chemical class 0.000 claims description 2
- 229920006122 polyamide resin Polymers 0.000 claims description 2
- 229920005668 polycarbonate resin Polymers 0.000 claims description 2
- 239000004431 polycarbonate resin Substances 0.000 claims description 2
- 229920000570 polyether Polymers 0.000 claims description 2
- 229920005672 polyolefin resin Polymers 0.000 claims description 2
- 229920005749 polyurethane resin Polymers 0.000 claims description 2
- 229920000915 polyvinyl chloride Polymers 0.000 claims description 2
- 239000004800 polyvinyl chloride Substances 0.000 claims description 2
- 229920002050 silicone resin Polymers 0.000 claims description 2
- 229920002554 vinyl polymer Polymers 0.000 claims description 2
- 239000002245 particle Substances 0.000 description 15
- 239000000843 powder Substances 0.000 description 13
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 13
- 238000010438 heat treatment Methods 0.000 description 10
- 229910000831 Steel Inorganic materials 0.000 description 7
- 239000000853 adhesive Substances 0.000 description 7
- 230000001070 adhesive effect Effects 0.000 description 7
- 239000010959 steel Substances 0.000 description 7
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 6
- ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 description 6
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 5
- 238000004519 manufacturing process Methods 0.000 description 5
- 238000012856 packing Methods 0.000 description 5
- 239000007787 solid Substances 0.000 description 5
- 239000002904 solvent Substances 0.000 description 5
- 230000007547 defect Effects 0.000 description 4
- 238000003912 environmental pollution Methods 0.000 description 4
- QQVIHTHCMHWDBS-UHFFFAOYSA-N isophthalic acid Chemical compound OC(=O)C1=CC=CC(C(O)=O)=C1 QQVIHTHCMHWDBS-UHFFFAOYSA-N 0.000 description 4
- 238000003860 storage Methods 0.000 description 4
- 239000004094 surface-active agent Substances 0.000 description 4
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 3
- 241000758993 Equisetidae Species 0.000 description 3
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
- 238000005260 corrosion Methods 0.000 description 3
- 238000007602 hot air drying Methods 0.000 description 3
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 3
- 239000003960 organic solvent Substances 0.000 description 3
- 238000007581 slurry coating method Methods 0.000 description 3
- 239000005029 tin-free steel Substances 0.000 description 3
- 239000005028 tinplate Substances 0.000 description 3
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 2
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 2
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 2
- -1 aliphatic alcohols Chemical class 0.000 description 2
- IISBACLAFKSPIT-UHFFFAOYSA-N bisphenol A Chemical compound C=1C=C(O)C=CC=1C(C)(C)C1=CC=C(O)C=C1 IISBACLAFKSPIT-UHFFFAOYSA-N 0.000 description 2
- 125000004432 carbon atom Chemical group C* 0.000 description 2
- 230000000052 comparative effect Effects 0.000 description 2
- 238000007796 conventional method Methods 0.000 description 2
- 230000007797 corrosion Effects 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- 239000002184 metal Substances 0.000 description 2
- 229910052751 metal Inorganic materials 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- 229920000728 polyester Polymers 0.000 description 2
- 238000007665 sagging Methods 0.000 description 2
- 229920005992 thermoplastic resin Polymers 0.000 description 2
- 229920001187 thermosetting polymer Polymers 0.000 description 2
- IDWKZTXLMMMQAJ-UHFFFAOYSA-N 1-butoxybutane formaldehyde urea Chemical compound C(CCC)OCCCC.C=O.NC(=O)N IDWKZTXLMMMQAJ-UHFFFAOYSA-N 0.000 description 1
- BRLQWZUYTZBJKN-UHFFFAOYSA-N Epichlorohydrin Chemical compound ClCC1CO1 BRLQWZUYTZBJKN-UHFFFAOYSA-N 0.000 description 1
- 241000195955 Equisetum hyemale Species 0.000 description 1
- 229910001335 Galvanized steel Inorganic materials 0.000 description 1
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical group [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 1
- JHWNWJKBPDFINM-UHFFFAOYSA-N Laurolactam Chemical compound O=C1CCCCCCCCCCCN1 JHWNWJKBPDFINM-UHFFFAOYSA-N 0.000 description 1
- 229920000299 Nylon 12 Polymers 0.000 description 1
- 239000004698 Polyethylene Substances 0.000 description 1
- BCKXLBQYZLBQEK-KVVVOXFISA-M Sodium oleate Chemical compound [Na+].CCCCCCCC\C=C/CCCCCCCC([O-])=O BCKXLBQYZLBQEK-KVVVOXFISA-M 0.000 description 1
- 229920001807 Urea-formaldehyde Polymers 0.000 description 1
- 150000001338 aliphatic hydrocarbons Chemical class 0.000 description 1
- 229910052782 aluminium Inorganic materials 0.000 description 1
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
- 229910000147 aluminium phosphate Inorganic materials 0.000 description 1
- 238000005452 bending Methods 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- QHIWVLPBUQWDMQ-UHFFFAOYSA-N butyl prop-2-enoate;methyl 2-methylprop-2-enoate;prop-2-enoic acid Chemical compound OC(=O)C=C.COC(=O)C(C)=C.CCCCOC(=O)C=C QHIWVLPBUQWDMQ-UHFFFAOYSA-N 0.000 description 1
- KRVSOGSZCMJSLX-UHFFFAOYSA-L chromic acid Substances O[Cr](O)(=O)=O KRVSOGSZCMJSLX-UHFFFAOYSA-L 0.000 description 1
- 238000002485 combustion reaction Methods 0.000 description 1
- 239000007859 condensation product Substances 0.000 description 1
- 239000008367 deionised water Substances 0.000 description 1
- 229910021641 deionized water Inorganic materials 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 239000000428 dust Substances 0.000 description 1
- AWJWCTOOIBYHON-UHFFFAOYSA-N furo[3,4-b]pyrazine-5,7-dione Chemical compound C1=CN=C2C(=O)OC(=O)C2=N1 AWJWCTOOIBYHON-UHFFFAOYSA-N 0.000 description 1
- 239000008397 galvanized steel Substances 0.000 description 1
- LNEPOXFFQSENCJ-UHFFFAOYSA-N haloperidol Chemical compound C1CC(O)(C=2C=CC(Cl)=CC=2)CCN1CCCC(=O)C1=CC=C(F)C=C1 LNEPOXFFQSENCJ-UHFFFAOYSA-N 0.000 description 1
- 150000002576 ketones Chemical class 0.000 description 1
- 239000002655 kraft paper Substances 0.000 description 1
- FPYJFEHAWHCUMM-UHFFFAOYSA-N maleic anhydride Chemical compound O=C1OC(=O)C=C1 FPYJFEHAWHCUMM-UHFFFAOYSA-N 0.000 description 1
- 239000012046 mixed solvent Substances 0.000 description 1
- 229920001568 phenolic resin Polymers 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 239000007921 spray Substances 0.000 description 1
- 238000007592 spray painting technique Methods 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
- 229920001169 thermoplastic Polymers 0.000 description 1
- 239000004416 thermosoftening plastic Substances 0.000 description 1
- 238000004065 wastewater treatment Methods 0.000 description 1
- 238000003466 welding Methods 0.000 description 1
- 238000009736 wetting Methods 0.000 description 1
Landscapes
- Application Of Or Painting With Fluid Materials (AREA)
Description
【発明の詳細な説明】
本発明は、溶接缶の側面つぎ四部の欠陥を補正する為の
鉄部の被覆方法に関する。DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a method of coating iron parts for correcting defects on the side edges of a welded can.
溶接缶の缶胴は、通常、方形に切断した鋼板材を筒形に
曲げ、該方形の対向辺部を重ね合わせてつぎ四部とし、
このつぎ四部を溶接する方法によって作る。The can body of a welded can is usually made by bending a steel plate cut into a rectangle into a cylindrical shape, overlapping the opposite sides of the rectangle to form four parts, and
It is made by welding the next four parts.
従ってそのつぎ四部には、缶素材としてティンフリース
チールのような防食処理を施した鋼材を用いる場合でも
、素材の切断端部(カットエツジ)或いは溶接金属等か
ら腐食が発生する可能性があり、従って何等かの手段に
より、これを防止する必要がある。Therefore, even if anti-corrosion treated steel such as tin-free steel is used as the material for the can, corrosion may occur from the cut edges of the material or the welded metal. It is necessary to prevent this by some means.
上記の腐食防止の手段として、従来、塗膜形成物質を有
機溶剤に溶解又は分散させた溶液型塗料、或いは粉体塗
料を用いて該つぎ四部を被覆する方法は知られている。As a means for preventing the above-mentioned corrosion, it is conventionally known to coat these four parts with a solution-type paint or a powder paint in which a film-forming substance is dissolved or dispersed in an organic solvent.
しかしながら溶接缶のつぎ四部には、缶素材のカットエ
ツジ部の重ね合わせによる段差があり、溶液型塗料或い
は粉体塗料を使用して、この段差を完全に被覆できる程
度の膜厚に塗装すると、塗膜に種々の欠陥を生じる。However, there is a level difference in the next four parts of the welded can due to the overlapping of the cut edges of the can material, and if you use solution-based paint or powder paint to coat this level difference completely, the coating will not work. This causes various defects in the film.
即ち、溶液型塗料は、厚塗りすると、10〜20μ程度
の膜厚でさえ、塗膜焼付けの際の加熱時に泡が発生し、
又、フレ或いは流下が生じてカットエツジを充分に被覆
することができない。In other words, when solution-based paints are applied thickly, even with a film thickness of about 10 to 20 microns, bubbles are generated during heating during coating baking.
Further, the cut edge cannot be sufficiently covered due to the occurrence of deflection or flow.
粉体塗料も、30〜70μ程度の厚塗りに対して成膜性
が充分でなく、ピンホールを発生し易い。Powder coatings also do not have sufficient film-forming properties for thick coatings of about 30 to 70 μm, and pinholes are likely to occur.
その他、溶液型塗料においては、溶剤による火災の危険
及び環境汚染のおそれがあり、その防止の為に特別な設
備を必要とする。In addition, solution-based paints pose a risk of fire and environmental pollution due to the solvent, and special equipment is required to prevent them.
粉体塗料の場合にも粉塵による環境汚染の問題を回避す
る為に設備を要し、又、粉体を高速かつ安定に輸送する
ことが困難であるという欠点を有する。Powder coatings also require equipment to avoid the problem of environmental pollution due to dust, and also have the disadvantage that it is difficult to transport the powder at high speed and stably.
従って本発明の目的は、溶接缶のつぎ四部の段差を、ピ
ンホールのような欠陥のない被膜で完全に被覆する方法
を提供するにある。SUMMARY OF THE INVENTION Accordingly, it is an object of the present invention to provide a method for completely covering the four steps of a welded can with a coating free of defects such as pinholes.
更に本発明の目的は、火災或いは環境汚染のおそれがな
く簡単容易に、溶接缶つぎ四部に被覆を施す方法を提供
するにある。A further object of the present invention is to provide a method for simply and easily coating the four parts of a welded can without the risk of fire or environmental pollution.
本発明者等は、上記目的を達成する為に、研究の結果、
溶接缶の側面つぎ白部をスラリー塗料の塗膜で被覆する
ならば、タレを生じることなく、かつ、塗膜に、泡、ハ
ジキ、ひび割れ等の欠陥を発生することなく、溶接缶側
面のつぎ白部の段差を完全に被覆するに充分な膜厚で被
覆でき、カットエツジの補正も完全に行い得る、という
ことを見出した。In order to achieve the above purpose, the present inventors, as a result of research,
If the white part of the side of the welded can is coated with a coating film of slurry paint, the next part of the side of the welded can can be coated without sagging or defects such as bubbles, cissing, and cracks in the coating. It has been found that the film can be coated with a film thickness sufficient to completely cover the steps in the white area, and that the cut edge can also be completely corrected.
即ち、本発明は溶接缶の側面つぎ白部を被覆する方法に
おいて、該つぎ白部にスラリー塗料を適用した塗料を乾
燥及び/又はセットし、次いで該乾燥及び/又はセット
したスラリー塗料の塗膜形成物質の融点又は軟化点以上
に加熱して、膜厚10〜100μの塗膜を形成せしめる
ことを特徴とする方法である。That is, the present invention provides a method for coating a white part of a welded can by drying and/or setting a slurry paint applied to the white part, and then applying a coating film of the dried and/or set slurry paint to the white part. This method is characterized by forming a coating film with a thickness of 10 to 100 μm by heating the material to a temperature higher than its melting point or softening point.
本明細書において、スラリー塗料とは、0.1〜5.0
μの粒径に粉体化された塗膜形成物質を、液状媒体中に
懸濁状に分散させた塗料を意味する。In this specification, slurry paint refers to 0.1 to 5.0
It means a paint in which a film-forming substance powdered to a particle size of μ is dispersed in a liquid medium in a suspension state.
本発明においては、公知の、任意のスラリー塗料を使用
することができる。In the present invention, any known slurry paint can be used.
本発明において使用し得るスラリー塗料の好ましい例は
、例えば熱可塑性ポリエステル樹脂、アクリル樹脂、ポ
リオレフィン樹脂、ポリ塩化ビニル樹脂、ポリアミド樹
脂、酢酸ビニル樹脂、ポリビニルアセクール樹脂、ポリ
エーテル樹脂、ポリカーボネート樹脂、エポキシ樹脂、
アルキド樹脂ホリウレタン樹脂、エポキシエステル樹脂
、フェノール樹脂、アミノ樹脂、及びケイ素樹脂のよう
な熱可塑性又は熱硬化性樹脂の、0.1〜50μ、好ま
しくは0.2〜20μ、更に好ましくは0.5〜10μ
の粒径を有する粒子を、水中に分散させた水性スラリー
塗料である。Preferred examples of slurry coatings that can be used in the present invention include thermoplastic polyester resins, acrylic resins, polyolefin resins, polyvinyl chloride resins, polyamide resins, vinyl acetate resins, polyvinyl acecool resins, polyether resins, polycarbonate resins, and epoxy resins. resin,
0.1-50μ, preferably 0.2-20μ, more preferably 0.1-50μ, more preferably 0.1-50μ, more preferably 0.1-50μ, preferably 0.2-20μ, more preferably 0.1-50μ, more preferably 0.1-50μ, preferably 0.2-20μ, more preferably 0.1-50μ, more preferably 0.1-50μ, more preferably 0.1-50μ, more preferably 0.2-20μ, more preferably 0.1-50μ, more preferably 0.2-20μ, more preferably 0.1-50μ, more preferably 0.1-50μ, more preferably 0.1-50μ, more preferably 0.1-50μ, more preferably 0.2-20μ, more thermoplastic or thermosetting resins such as alkyd resins, polyurethane resins, epoxy ester resins, phenolic resins, amino resins, and silicone resins. 5~10μ
This is an aqueous slurry paint made by dispersing particles with a particle size of .
該水性スラリー塗料は、少量の界面活性剤及び。The water-based slurry paint contains a small amount of surfactant and.
又は少量の水可溶性有機溶剤を含有することができる。Alternatively, it may contain a small amount of a water-soluble organic solvent.
界面活性剤を塗膜形成物質粒子の分散を助け、塗料の安
定性を改善する作用をし、有機溶剤は、塗料のヌレ及び
成膜性を高める。The surfactant helps disperse the film-forming substance particles and improves the stability of the paint, and the organic solvent improves the wetting and film-forming properties of the paint.
しかしながら本発明においては、前記例示のような樹脂
粒子を溶解しない有機液体、例えば、ブタノール、プロ
パツールのような、炭素数1〜5の脂肪族アルコール類
、ヘキサンのような炭素数6〜8の脂肪族炭化水素類又
はアセトンのようなケトン類を媒体とするスラリー塗料
を使用することもできる。However, in the present invention, organic liquids that do not dissolve the resin particles, such as aliphatic alcohols having 1 to 5 carbon atoms such as butanol and propatool, and 6 to 8 carbon atoms such as hexane, are used. Slurry coatings based on aliphatic hydrocarbons or ketones such as acetone can also be used.
本発明において使用されるスラリー塗料の固形分濃度は
通常5〜70重量%、好ましくは10〜50重量%、更
に好ましくは20〜40重量%である。The solid content concentration of the slurry paint used in the present invention is usually 5 to 70% by weight, preferably 10 to 50% by weight, and more preferably 20 to 40% by weight.
本発明においては、上述のスラリー塗料を、最終塗膜の
膜厚が10〜100μ、好ましくは20〜80μ、より
好ましくは30〜70μとなる厚さに、溶接缶側面のつ
ぎ白部に適用され、セットされる。In the present invention, the above-mentioned slurry paint is applied to the white part of the welded can side surface to a thickness such that the final coating film has a thickness of 10 to 100μ, preferably 20 to 80μ, more preferably 30 to 70μ. , is set.
塗膜の膜厚が10μ以下では、段差のカットエツジが補
正されないで露出部分が生じるおそれがある。If the thickness of the coating film is 10 μm or less, there is a risk that the cut edge of the step will not be corrected and an exposed portion will be formed.
100μ以上の膜厚がしようとする泡が発生し易く、タ
レも生じ易くなる。If the film thickness is 100 μm or more, bubbles are likely to occur and sagging is also likely to occur.
スラリー塗料を、溶接缶側面のつぎ白部に適用する方法
自体には格別制限はなく、公知の任意の方法、例えばエ
アスプレー、エアレススプレーロールコート、又は等の
方法が随時使用できる。There are no particular restrictions on the method of applying the slurry paint to the white area on the side surface of the welded can, and any known method such as air spraying, airless spray roll coating, or the like can be used at any time.
上述のようにして、被塗物表面に適用され、セットされ
た塗料は、次いで、必要に応じ乾燥を行なった後、塗膜
形成工程に付される。The paint that has been applied and set on the surface of the object to be coated as described above is then dried if necessary, and then subjected to a film forming step.
塗膜形成工程は、使用するスラリー塗料の塗膜形成物質
が熱可塑性樹脂である場合には、その融点以上の温度、
そして塗膜形成物質が熱硬化性樹脂である場合には、そ
の軟化点以上の温度に、セットされた塗料を加熱するこ
とにより行われる。When the coating film forming substance of the slurry paint used is a thermoplastic resin, the coating film forming process is carried out at a temperature higher than the melting point of the thermoplastic resin,
When the coating film-forming substance is a thermosetting resin, the coating is heated to a temperature equal to or higher than its softening point.
この加熱温度は使用する塗料の塗膜形成物質樹脂の種類
により異なり、例えば、熱可塑性ポリエステル樹脂を塗
膜形成物質とするスラリー塗料の場合には100°〜5
00℃の温度、好ましくは1200〜350°、更に好
ましくは150°〜300℃の温度である。This heating temperature varies depending on the type of film-forming substance resin in the paint used; for example, in the case of a slurry paint whose film-forming substance is thermoplastic polyester resin, it is 100° to 5°C.
00°C, preferably 1200° to 350°C, more preferably 150° to 300°C.
この塗膜形成の為の加熱手段については、例えば、熱風
炉加熱、ガスバーナー加熱、赤外線加熱又は高周波加熱
等の公知の加熱手段が随時使用でき、格別の制限はない
。As for the heating means for forming the coating film, any known heating means such as hot air oven heating, gas burner heating, infrared heating, or high frequency heating can be used as needed, and there are no particular limitations.
しかしながら、ガスバーナーによる直接局部加熱が有利
である。However, direct local heating with gas burners is advantageous.
スラリー塗料を用いる本発明の溶接缶側面のつぎ白部の
被覆方法は、従来の溶液型塗料或いは粉体塗料を用いる
被覆方法に比べ、泡、ノ・ジキ、ピンホール又はひ又割
れのような欠陥のない優れた塗膜が厚膜で得られ、従っ
てつぎ白部が欠陥のない塗膜により完全に被覆されると
いう効果を有する他、被塗物に対し、高速適用が可能で
あり、火災の危険或いは環境汚染のおそれがなく、従っ
て特別の排気燃焼設備を要せず、未使用塗料の回収や、
排水処理が容易であり、更に、溶剤型塗料の塗装設備を
そのま又使用して一回塗りで厚膜の塗膜を得ることがで
きる等の利点が得られる。The coating method of the present invention using a slurry coating for the white area on the side surface of a welded can is more effective than the coating method using a conventional solution-type coating or powder coating, since it does not cause problems such as bubbles, chips, pinholes, or cracks. In addition to being able to obtain a thick, defect-free and excellent coating film, which ensures that the next white area is completely covered with a defect-free coating film, it is also possible to apply the coating at high speed to the object being coated, and to prevent fires. There is no risk of danger or environmental pollution, therefore, there is no need for special exhaust combustion equipment, and it is possible to collect unused paint,
It has advantages such as easy wastewater treatment and the ability to obtain a thick coating film in one coat using solvent-based coating equipment.
本発明の溶接缶の側面つぎ四部被覆方法は、任意の金属
缶、例えば、ブリキ材、ティンフリースティール材(ク
ロムメッキ鋼板)、ブラックプレート材(未処理鋼板)
、アルミ材、クロム酸、リン酸で化学処理した鋼板、亜
鉛メッキ鋼板、等を素材とする溶接缶に適用することが
できる。The method of covering the sides and four parts of a welded can according to the present invention can be applied to any metal can, such as tinplate, tin-free steel (chrome-plated steel), black plate (untreated steel).
It can be applied to welded cans made of materials such as aluminum, steel sheets chemically treated with chromic acid or phosphoric acid, and galvanized steel sheets.
以下に実施例をおけて本発明を更に説明する。The present invention will be further explained below with reference to Examples.
参考例 1
(水スラリー塗料Aの製造)
数平均分子量55000、融点130℃の無水マレイン
酸クラフトポリエチレンを粉砕して、平均粒径3μ(最
大粒径10μ)の粉体とし、これを脱イオン水中に、界
面活性剤(オレイン酸ソーダ)0.1部と共に加えて強
制分散させ、水スラリー塗料Aを得た。Reference Example 1 (Manufacture of water slurry paint A) Maleic anhydride kraft polyethylene with a number average molecular weight of 55,000 and a melting point of 130°C is ground into a powder with an average particle size of 3 μm (maximum particle size of 10 μm), and this is poured into deionized water. A water slurry paint A was obtained by adding 0.1 part of a surfactant (sodium oleate) and forcibly dispersing the mixture.
固形分は48%で、粒度は33 cps (25℃)で
あった。The solids content was 48% and the particle size was 33 cps (25°C).
参考例 2
(水スラリー塗料Bの製造)
イソフタル酸とプロピレングリコールの縮合物である、
数平均分子量62000、融点132℃のポリエステル
を粉砕し、平均粒径2μ(最大粒径16μ)の粉体とし
、これを界面活性剤(モダンロー・モンサント化成会社
製)0゜2部と共に、脱イオン水中に加えて強制分散さ
せ、水スラリー塗料Bを得た。Reference Example 2 (Manufacture of water slurry paint B) A condensate of isophthalic acid and propylene glycol,
Polyester with a number average molecular weight of 62,000 and a melting point of 132°C is ground into a powder with an average particle size of 2μ (maximum particle size of 16μ), which is deionized together with 0°2 parts of a surfactant (Modern Law Monsanto Chemical Co., Ltd.). It was added to water and forcedly dispersed to obtain water slurry paint B.
固形分は40%で、粒度は29cps (25℃)であ
った。The solids content was 40% and the particle size was 29 cps (25°C).
参考例 3
(溶剤スラリー塗料Cの製造)
平均分子量53000.融点172℃のナイロン12樹
脂を粉砕し、平均粒径4μ(最大粒径18μ)の粉体を
得、n−ブチルアルコール中に分散せしめ、固形分35
%の溶剤スラリー塗料Cを得た。Reference Example 3 (Manufacture of solvent slurry paint C) Average molecular weight 53000. Nylon 12 resin with a melting point of 172°C was crushed to obtain a powder with an average particle size of 4 μm (maximum particle size of 18 μm), and dispersed in n-butyl alcohol to reduce the solid content to 35 μm.
% solvent slurry paint C was obtained.
参考例 4
(溶液型塗料りの製造)
ビスフェノールAとエピクロルヒドリンとの縮合生成物
で、数平均分子量2900のエポキシ樹脂(エピコー)
1007・シェル化学社製)75部と、ブチルエーテル
尿素ホルムアルデヒド樹脂(スーパーベッカミンP−1
38・犬日本インキ製)25部を、メチルエチルケトン
50部、トルエン50部の混合溶剤に溶解させて、固形
分25%の溶液型塗料りを得た。Reference Example 4 (Production of solution-type paint) Epoxy resin (Epicor) which is a condensation product of bisphenol A and epichlorohydrin and has a number average molecular weight of 2900.
1007 manufactured by Shell Chemical Co., Ltd.) and 75 parts of butyl ether urea formaldehyde resin (Super Beckamine P-1
38 (manufactured by Inu Nippon Ink) was dissolved in a mixed solvent of 50 parts of methyl ethyl ketone and 50 parts of toluene to obtain a solution-type paint with a solid content of 25%.
参考例 5
(粉体塗料Eの製造)
イソフタル酸とプロピレングリコールの縮合物である、
数平均分子量62000.融点132℃のポリエステル
を粉砕し、平均粒径15μ(最大粒径80μ)の粉体塗
料Eを得た。Reference Example 5 (Manufacture of powder coating E) A condensate of isophthalic acid and propylene glycol,
Number average molecular weight 62000. A polyester having a melting point of 132° C. was ground to obtain a powder coating E having an average particle size of 15 μm (maximum particle size of 80 μm).
実施例 1
板厚(0,26mm)のブリキ板に、エポキシフェノー
ル系塗料(エポキシ系樹脂とフェノール樹脂の比率1:
1の混合物)を、缶胴のつぎ目部分にあたる場所を除い
て、焼付後の膜厚が内面側5ミクロン、外面側3ミクロ
ンになるようにマージン塗装し、200℃の熱風乾燥炉
中で10分間焼付硬化させて得られた、前記ブリキ材の
塗装板を、さげ4号缶のボデーブランク(ブランクレン
グス238.33mm、ブランクバイト122.22m
m)に切断し、ロールフォーマ−により円筒状にし、そ
の側端を0.4mm重ね合わせ、溶接加工して缶胴を作
成した。Example 1 A tin plate with a thickness of 0.26 mm was coated with epoxyphenol paint (the ratio of epoxy resin to phenol resin was 1:
1 mixture) was coated on the margins of the can body, except for the seam area, so that the film thickness after baking was 5 microns on the inner surface and 3 microns on the outer surface, and then dried in a hot air drying oven at 200°C for 10 minutes. The painted tin plate obtained by baking and hardening for a minute was used to make a body blank for a No. 4 can (blank length 238.33 mm, blank bite 122.22 m).
m) was cut into a cylindrical shape using a roll former, and the side ends were overlapped by 0.4 mm and welded to create a can body.
前記方法で得られた缶胴の内面及び外面のつぎ目部分を
、エアレスガンにより巾10mm、乾燥塗膜の厚みが4
0〜60ミクロンになるように、参考例1の水スラリー
塗料Aをスプレィ塗装した後、180℃の熱風乾燥炉中
で3分間焼付け、つぎ目隣接部分上に接着性線条被覆物
を作成した。The seam portions of the inner and outer surfaces of the can body obtained by the above method were coated with an airless gun to a width of 10 mm and a dry coating thickness of 4 mm.
After spray painting the water slurry paint A of Reference Example 1 to a thickness of 0 to 60 microns, it was baked in a hot air drying oven at 180°C for 3 minutes to create an adhesive striped coating on the area adjacent to the seam. .
そして、上記被覆物の塗膜状態を観察し、硫酸鋼溶液に
よってカットエツジカバレージ性を調べた。Then, the coating state of the above coating was observed, and the cut edge coverage was examined using a sulfuric acid steel solution.
更に、上記方法によって得られた缶胴を常法によりフラ
ンジ加工した後、同じく常法により得られた、内外面に
エポキシフェノール系塗膜を有する301径のブリキ蓋
を二重巻締めし、得られた空缶にさげ水煮をパックし、
上記301径と同様のブリキ蓋を二重巻締めし、それぞ
れ121℃で90分間レトルト処理を行った。Furthermore, the can body obtained by the above method was flanged by a conventional method, and then a 301 diameter tin lid, which was also obtained by a conventional method and had an epoxyphenol coating on the inner and outer surfaces, was double-sealed. Pack the samurai in empty cans.
A tin lid similar to the above 301 diameter was double-sealed, and retort treatment was performed at 121° C. for 90 minutes.
上記レトルト処理を行ったパック缶(各200缶)を、
レトルト処理直後及び50℃1年間貯蔵した後開缶し、
缶胴つぎ目部分の塗膜状態を観察した。Packed cans (200 cans each) that have undergone the above retort treatment,
Open the can immediately after retorting and after storing it at 50℃ for 1 year.
The condition of the coating film on the joint part of the can body was observed.
それぞれの結果を下記表1に示す。The respective results are shown in Table 1 below.
実施例 2
実施例1と同様な方法で得られたブリキ缶胴の内面及び
外面のつぎ目部分に、エアレスガンにより実施例工と同
様な条件で、参考例2の水スラリー塗料Bを塗装し、前
記缶胴つぎ目隣接部分上に接着性線条被覆物を作成した
。Example 2 Water slurry paint B of Reference Example 2 was applied to the seam parts of the inner and outer surfaces of a tin can body obtained in the same manner as in Example 1 using an airless gun under the same conditions as in the Example. An adhesive striped coating was created on the can body adjacent to the seam.
実施例1と同様、前記缶胴つぎ目部分の塗膜状態、カッ
トエツジカバレージ性を調べ、更にさげ水煮をパックし
、レトルト直後及び50°C11年間貯蔵後の塗膜状態
を観察した。In the same manner as in Example 1, the state of the coating film at the seam of the can body and the cut edge coverage were examined, and the state of the coating film was also observed immediately after retorting and after storing at 50° C. for 11 years after packing the samurai in water.
それぞれの結果を下記表1に示す。実施例 3
実施例1と同様な方法で得られたブリキ缶胴の内面及び
外面のつぎ目部分に、エアレスガンにより実施例1と同
様な条件で、参考例3の・溶剤スラリー塗料Cを塗装し
、前記缶胴つぎ目隣接部分上に接着性線条被覆物を作成
した。The respective results are shown in Table 1 below. Example 3 Solvent slurry paint C of Reference Example 3 was applied to the seam parts of the inner and outer surfaces of a tin can body obtained in the same manner as in Example 1 using an airless gun under the same conditions as in Example 1. , an adhesive striped coating was created on the portion adjacent to the can body seam.
実施例1と同様、前記缶胴つぎ目部分の塗膜状態、カッ
トエツジのカバレージ性を調べ、更に、さげ水煮をパッ
クし、レトルト直後及び50℃、1年間貯蔵後の塗膜状
態を観察した。In the same manner as in Example 1, the state of the coating film at the seam of the can body and the coverage of the cut edges were examined, and the state of the coating film was also observed after packing the boiled horsetails and observing them immediately after retorting and after storage at 50°C for one year. .
それぞれの結果を下記表1に示す。The respective results are shown in Table 1 below.
実施例 4
板厚(0,26mm)のティンフリースチール板を、実
施例1と同様な方法で溶接加工し、得られた缶胴の内面
及び外面のつぎ目部分に、エアレスガンにより実施例1
と同様な条件で、参考例1の水スラリー塗料Aを塗装し
、前記缶胴つぎ目隣接部分上に接着性線条被覆物を作成
した。Example 4 A tin-free steel plate with a thickness of 0.26 mm was welded in the same manner as in Example 1, and the seams of the inner and outer surfaces of the resulting can body were welded using an airless gun.
Under the same conditions as above, the water slurry paint A of Reference Example 1 was applied to form an adhesive striped coating on the portion adjacent to the seam of the can body.
実施例1と同様、前記缶胴つぎ目部分の塗膜状態、カッ
トエツジのカバレージ性を調べ、更に、さげ水煮をパッ
クし、レトルト直後及び50℃、1年間貯蔵後の塗膜状
態を観察した。In the same manner as in Example 1, the state of the coating film at the seam of the can body and the coverage of the cut edges were examined, and the state of the coating film was also observed after packing the boiled horsetails and observing them immediately after retorting and after storage at 50°C for one year. .
それぞれの結果を下記表1に示す。The respective results are shown in Table 1 below.
実施例 5
板厚(0,26mm)のブラックプレート(未処理オ哀
鋼板)板を、実施例1と同様な方法で溶接加工し、得ら
れた缶胴の内面及び外面のつぎ目部分に、エアレスガン
により実施例1と同様な条件で、参考例1の水スラリー
塗料Aを塗装し、前記缶胴つぎ置部隣接部分上に接着性
線条被覆物を作成した。Example 5 A black plate (untreated steel plate) with a thickness of 0.26 mm was welded in the same manner as in Example 1, and the joints on the inner and outer surfaces of the resulting can body were coated with the following: The water slurry paint A of Reference Example 1 was applied using an airless gun under the same conditions as in Example 1 to create an adhesive striped coating on the area adjacent to the can body splicing area.
実施例1と同様、前記缶胴つぎ目部分の塗膜状態、カッ
トエツジのカバレージ性を調べ、更に、さげ水煮をどく
ツクし、レトルト直後及び50℃、1年間貯蔵後の塗膜
状態を観察した。In the same manner as in Example 1, the state of the coating film at the seam of the can body and the coverage of the cut edge were investigated, and the state of the coating film was further observed after boiling in water and after retorting and after storage at 50°C for one year. did.
それぞれの結果を下記表1に示す。The respective results are shown in Table 1 below.
比較例 1
実施例1と同様な方法で得られたブリキ缶胴の内面及び
外面のつぎ目部分に、エアレスガンにより実施例1と同
様な条件で、参考例4の溶液型塗料を塗装し、前記缶胴
つぎ目隣接部分上に接着性線条被覆物を作成した。Comparative Example 1 The solution-type paint of Reference Example 4 was applied to the seam portions of the inner and outer surfaces of a tin can body obtained in the same manner as in Example 1 using an airless gun under the same conditions as in Example 1. An adhesive striation coating was created on the can body adjacent to the seam.
実施例1と同様、前記缶胴つぎ目部分の塗膜状態、カッ
トエツジのカバレージ性を調べ、更に、さげ水煮をパッ
クし、レトルト直後及び50℃、1年間貯蔵後の塗膜状
態を観察した。In the same manner as in Example 1, the state of the coating film at the seam of the can body and the coverage of the cut edges were examined, and the state of the coating film was also observed after packing the boiled horsetails and observing them immediately after retorting and after storage at 50°C for one year. .
それぞれの結果を下記表1に示す。比較例 2
実施例1と同様な方法で得られたブリキ缶胴の、内面の
つぎ目部分に、粉体塗装ガンにより巾10關、乾燥塗膜
の厚みが30〜50ミクロンになるように、参考例5の
粉体塗料Eを塗装した後、180°Cの熱風乾燥炉中で
15分間焼付け、つぎ目隣接部分上に接着性線条被覆物
を作成した。The respective results are shown in Table 1 below. Comparative Example 2 A tin can body obtained in the same manner as in Example 1 was coated with a powder coating gun on the seam part of the inner surface so that the width was 10 mm and the thickness of the dried coating was 30 to 50 microns. After applying the powder coating E of Reference Example 5, it was baked for 15 minutes in a hot air drying oven at 180°C to form an adhesive striped coating on the area adjacent to the seam.
実施例1と同様、前記缶胴つぎ目部分の塗膜状態、カッ
トエツジのカバレージ性を調べ、更に、さげ水煮をパッ
クし、レトルト直後及び50°c、1年間貯蔵後の塗膜
状態を観察した。As in Example 1, the state of the coating on the seam of the can body and the coverage of the cut edges were examined, and the state of the coating was further observed after packing the boiled horsetail and storing it immediately after retorting and at 50°C for one year. did.
それぞれの結果を下記表1に示す。The respective results are shown in Table 1 below.
Claims (1)
該?ぎ四部にスラリー塗料を適用し、適用した塗料を乾
燥及び/又はセットし、次いで該乾燥及び/又はセット
したスラリー塗料の塗膜形ff物質の融点または軟化点
以上に加熱して膜厚10〜100μの塗膜を形成せしめ
ることを特徴とする方法。 2 スラリー塗料の塗膜形成物質が、熱可塑性ポリエス
テル樹脂、アクリル樹脂、ポリオレフィン樹脂、ポリ塩
化ビニル樹脂、ポリアミド樹脂、酢酸ビニル樹脂、ポリ
ビニルアセクール樹脂、ポリエーテル樹脂、ポリカーボ
ネート樹脂、エポキシ樹脂、アルキド樹脂、ポリウレタ
ン樹脂、エポキシエステル樹脂、フェノール樹脂、アミ
ノ樹脂及びケイ素樹脂からなる群の少くとも一つから選
ばれる特許請求の範囲第1項記載の方法。 3 スラリー塗料が水性スラリー塗料である特許請求の
範囲第1項又は第2項記載の方法。[Claims] 1. A method for covering four parts of a side seam of a welded can,
Applicable? A slurry paint is applied to the four parts, the applied paint is dried and/or set, and then the dried and/or set slurry paint is heated to a temperature higher than the melting point or softening point of the film-forming material of the slurry paint to form a film with a thickness of 10 to 10. A method characterized by forming a coating film of 100μ. 2 The film-forming substance of the slurry paint is a thermoplastic polyester resin, acrylic resin, polyolefin resin, polyvinyl chloride resin, polyamide resin, vinyl acetate resin, polyvinyl acecool resin, polyether resin, polycarbonate resin, epoxy resin, alkyd resin. 2. The method according to claim 1, wherein the resin is selected from at least one of the group consisting of polyurethane resin, epoxy ester resin, phenol resin, amino resin, and silicone resin. 3. The method according to claim 1 or 2, wherein the slurry paint is an aqueous slurry paint.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP5440678A JPS5855832B2 (en) | 1978-05-10 | 1978-05-10 | How to cover the side seams of welded cans |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP5440678A JPS5855832B2 (en) | 1978-05-10 | 1978-05-10 | How to cover the side seams of welded cans |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS54146836A JPS54146836A (en) | 1979-11-16 |
| JPS5855832B2 true JPS5855832B2 (en) | 1983-12-12 |
Family
ID=12969811
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP5440678A Expired JPS5855832B2 (en) | 1978-05-10 | 1978-05-10 | How to cover the side seams of welded cans |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS5855832B2 (en) |
Families Citing this family (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS5674436A (en) * | 1979-11-19 | 1981-06-19 | Toyo Seikan Kaisha Ltd | Welded can and its manufacture |
| JPS6049425B2 (en) * | 1980-06-12 | 1985-11-01 | 東洋製罐株式会社 | Tein-free steel welded can with coated seams |
| JPS5768344A (en) * | 1980-10-04 | 1982-04-26 | Hokkai Can | Inner surface correction welding can body and its manufacture |
| JPS5780045A (en) * | 1980-11-06 | 1982-05-19 | Dainichi Seikan Kk | Method of forming drum of high corrosion-resisting can |
-
1978
- 1978-05-10 JP JP5440678A patent/JPS5855832B2/en not_active Expired
Also Published As
| Publication number | Publication date |
|---|---|
| JPS54146836A (en) | 1979-11-16 |
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