JPH02157067A - Method for peeling coating film - Google Patents

Method for peeling coating film

Info

Publication number
JPH02157067A
JPH02157067A JP31105088A JP31105088A JPH02157067A JP H02157067 A JPH02157067 A JP H02157067A JP 31105088 A JP31105088 A JP 31105088A JP 31105088 A JP31105088 A JP 31105088A JP H02157067 A JPH02157067 A JP H02157067A
Authority
JP
Japan
Prior art keywords
coating film
peeling
amine salt
solvent
heat treatment
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
JP31105088A
Other languages
Japanese (ja)
Inventor
Toshiyuki Ota
敏行 太田
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.)
Individual
Original Assignee
Individual
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 Individual filed Critical Individual
Priority to JP31105088A priority Critical patent/JPH02157067A/en
Publication of JPH02157067A publication Critical patent/JPH02157067A/en
Pending legal-status Critical Current

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Abstract

PURPOSE:To peel off even a strong crosslinking film efficiently, securely and stably by applying to a material with a coating film the treatment of peeling solution containing amine salt having 2 - 16 carbon numbers of fluoric acid, and more adequately heat treatment. CONSTITUTION:A material with a coating film is treated with peeling solution containing amine salt having 2 - 16 carbon atoms of fluoric acid and the coating film is peeled off. As the suitable examples of amine, trimethylamine, triethylamine, butylamine and the like are used, and 0.1 - 20wt.% amine salt is preferably used. Methylene chloride, fluorinated solvent and the like are the suitable examples of organic solvents for prepating a peeling solution. Peeling can be increased in the peeling solution by heat treatment, and the heat treatment at the temperature of boiling point or under of the solvent to be used is suitable.

Description

【発明の詳細な説明】 (産業上の利用分野) 本発明は塗膜の剥離法に関するものである。[Detailed description of the invention] (Industrial application field) The present invention relates to a method for removing paint films.

(従来技術) 塗装はアルミニウム系、鉄系その他の各種金属製品、そ
の他の素材製品の保護、防食、美装等を図るための手段
として不可欠である。この塗装としては、素地との密着
性や分子間の凝集力の面から架橋塗膜が優れているが、
塗料それ自体や塗装作業の不具合などなんらかの理由で
不良が発生した場合や、古い塗膜を新たにする場合には
、塗り直しのため金属素材から塗膜を剥すことが必要で
ある。ところが、架橋塗膜は分子が3次元結合している
ため強固である。このような塗膜の剥離法として、メチ
レンクロライドを主体とし、これに少量のギ酸又は弗化
アンモニウムを加えた溶剤性の液で処理する方法が知ら
れているが、ギ酸又は弗化アンモニウムは水溶性である
ため、非水溶性のメチレンクロライドとの相溶性が悪く
、このため両者の相乗効果が現れず、夫々単独に作用し
ており、剥離に時間がかかり、又剥離効果の安定性が乏
しいという欠点があり、その改善が強く要望されている
(Prior Art) Painting is indispensable as a means for protecting, anticorrosion, and beautifying aluminum-based, iron-based, and other various metal products, as well as other material products. Cross-linked coatings are superior in terms of adhesion to the substrate and cohesive force between molecules, but
If a defect occurs due to some reason such as a defect in the paint itself or the painting process, or if an old paint film is to be replaced with a new one, it is necessary to remove the paint film from the metal material for repainting. However, crosslinked coatings are strong because their molecules are three-dimensionally bonded. A known method for removing such paint films is to treat them with a solvent-based solution consisting mainly of methylene chloride and a small amount of formic acid or ammonium fluoride; however, formic acid or ammonium fluoride is water-soluble. Because of its chemical properties, it has poor compatibility with water-insoluble methylene chloride, and as a result, there is no synergistic effect between the two, and each acts independently, resulting in long peeling times and poor stability of the peeling effect. However, there is a strong demand for its improvement.

本発明は前記のような問題点を解決するために創案され
たもので、その目的とするところは、強固な架橋塗膜を
も効率良く確実に安定して剥離することができるこの種
塗膜剥離法を提供することにある。
The present invention was devised to solve the above-mentioned problems, and its purpose is to provide a coating film of this type that can efficiently, reliably and stably remove even strong cross-linked coatings. The object of the present invention is to provide a peeling method.

(問題を解決するための手段) 上記目的を達成するため本発明は、塗膜を有する金属等
の素材を、弗酸のC2〜C16のアミン塩を含有する剥
離液で処理、特に加熱処理することで塗膜を剥離するよ
うにしたものである。
(Means for solving the problem) In order to achieve the above object, the present invention treats a material such as a metal having a coating film with a stripping solution containing a C2 to C16 amine salt of hydrofluoric acid, in particular heat treatment. This allows the paint film to be peeled off.

具体的に説明すると、本発明の特徴は、弗酸のC2〜C
16のアミン塩を使用することである。この弗酸のC2
〜C16のアミン塩は、有機溶剤との良好な相溶性を有
し、これを併用することにより、架橋塗膜を膨潤させて
塗膜内に迅速に浸透し、3次元結合状態の塗膜分子を破
壊すると共に、金属等の素地をエッチングするため、塗
膜剥離が極めて容易、確実となり、剥離液の安定性も大
になる。
Specifically, the feature of the present invention is that C2 to C of hydrofluoric acid
16 amine salts are used. C2 of this hydrofluoric acid
The ~C16 amine salt has good compatibility with organic solvents, and when used together, it swells the crosslinked coating film and quickly penetrates into the coating film, forming coating molecules in a three-dimensionally bonded state. Since it destroys the metal and etches the base material such as metal, the coating film can be removed extremely easily and reliably, and the stability of the remover is also increased.

このために、弗酸のC2〜C16のアミン塩は不可欠で
ある。C1以下では有機溶剤との相溶性が悪くなるため
上記効果が現れず、C16を超えると弗酸との反応が遅
くなるため不適当である。
For this purpose, a C2 to C16 amine salt of hydrofluoric acid is essential. If it is less than C1, the above effect will not be achieved because the compatibility with the organic solvent will be poor, and if it exceeds C16, the reaction with hydrofluoric acid will be slow, which is inappropriate.

弗酸のC2〜C16のアミン塩としては、トリメチルア
ミン、トリエチルアミン、ジエチルアミン、ブチルアミ
ン、ヘキシルアミン、オクチルアミン、ラウリルアミン
などが代表的である。
Typical C2-C16 amine salts of hydrofluoric acid include trimethylamine, triethylamine, diethylamine, butylamine, hexylamine, octylamine, and laurylamine.

なお、C2〜C16のアミンは、アルカノールアミンを
含むものであり、その例としては、ジエタノールアミン
、トリエタノールアミンなどが挙げられる。
Note that the C2 to C16 amine includes alkanolamine, and examples thereof include diethanolamine, triethanolamine, and the like.

上記弗酸のC2〜C16のアミン酸の量は、重量比で大
体0.1%〜20%が適当である。0.1%未満では実
質的に剥離効果が望めなくなり、20%を超える量とす
ると剥離効果は大になるが、金属等の素材に対するエッ
チング性も大になるため好ましいとはいえない。
The amount of the C2 to C16 amine acid in the hydrofluoric acid is preferably about 0.1% to 20% by weight. If the amount is less than 0.1%, no peeling effect can be expected, and if it exceeds 20%, the peeling effect will be greater, but the etching property for materials such as metals will also be greater, which is not preferable.

有機溶剤は塗膜を膨潤させやすいものが好しく、メチレ
ンクロライド、トリクロルエチレン、パークロルエチレ
ン、弗素系溶剤、ケトン系溶剤、アノン系溶剤、ベンゾ
ール、トルオール等が普通であるが、メチレンクロライ
ドが膨潤性が大きく代表的である。
The organic solvent is preferably one that easily swells the coating film, and methylene chloride, trichloroethylene, perchloroethylene, fluorine solvents, ketone solvents, anone solvents, benzol, toluol, etc. are common, but methylene chloride swells the coating film easily. gender is highly representative.

しかし、本発明では、剥離液を加熱することにより、こ
の加熱の助けにより、剥離を著しく大にすることができ
るため、他の有機溶剤を使用することができる。加熱温
度は剥離液、特に使用溶剤の沸点以下であることが適当
である。
However, in the present invention, other organic solvents can be used since by heating the stripping solution, stripping can be significantly increased with the aid of this heating. The heating temperature is suitably below the boiling point of the stripping solution, especially the solvent used.

剥離液を使用中、液中の溶剤の蒸発はどうしても避けら
れない。特に加熱すると、この傾向が更に大になる。こ
のために溶剤を補給しなければならない。
When using a stripping solution, evaporation of the solvent in the solution is unavoidable. Especially when heated, this tendency becomes even more pronounced. For this purpose, solvent must be replenished.

この対策として、少量のパラフィンを加えて液面をシー
ルする方法が行れている。
As a countermeasure to this problem, a method is used to seal the liquid surface by adding a small amount of paraffin.

ところが、パラフィンが一部ハンガーヌは塗膜剥離した
金属等の素材に付着して電着塗料に混ざつて塗料に浮び
、塗装後の塗膜に付着して塗膜不良を生じ問題になって
いる。
However, some of the paraffin attached to materials such as metals from which the paint film has peeled off, mixed with the electrodeposited paint, floated on the paint, and adhered to the paint film after painting, causing paint film defects and causing problems. .

そこで、パラフィンの代りに水層でシールしたところ、
パラフィンによる塗膜不良はなくなるが、今度は剥離液
中の水溶性の蟻酸、弗化アンモニウムを水層が吸収して
しまい、非水溶性のメチレンクロライドのみが残存し、
剥離性が著しく弱くなつて使用不能になった。
So, when we sealed it with a water layer instead of paraffin,
Although the paint film defect caused by paraffin disappears, the water layer absorbs the water-soluble formic acid and ammonium fluoride in the stripping solution, leaving only water-insoluble methylene chloride.
The removability became extremely weak and it became unusable.

本発明はこの問題をも、剥離液として、弗酸のC2〜C
16のアミン塩と水より比重が重く、非水溶性の有機溶
剤、たとえば、メチレンクロライド、トリクロルエチレ
ン、パークロルエチレン、弗素系溶剤等を使用し、その
上に水層を設けてシールしても、弗酸のC2〜C16の
アミン塩は有機溶剤と良く相溶するため、水層に吸収さ
れる問題は著しく改善され、有機溶剤の使用量が大きく
節約され、剥離性が弱くなることもなくなる。
The present invention also solves this problem by using hydrofluoric acid as a C2-C
Even if the amine salt of No. 16 and a water-insoluble organic solvent with a specific gravity heavier than water, such as methylene chloride, trichloroethylene, perchloroethylene, or fluorine-based solvent, are used, a water layer is formed on top of the organic solvent, and the sealing is performed. , C2-C16 amine salts of hydrofluoric acid are well compatible with organic solvents, so the problem of absorption into the water layer is significantly improved, the amount of organic solvent used is greatly reduced, and the peelability is no longer weakened. .

特に加熱することにより剥離性が更に著しく大になる。In particular, heating significantly increases the releasability.

加熱は使用溶剤の沸点以下でしかも水の沸点以下が適切
である。
It is appropriate that the heating be carried out at a temperature below the boiling point of the solvent used and below the boiling point of water.

溶剤に溶解する重合触媒、たとえば、ベソゾイルパーオ
キサイド、過酸化ラウリル、アゾビスイソブチロニトリ
ル、t−ブチルパーオキサイド等を一部溶剤に加えると
剥離性が更に大になる。
If a portion of a polymerization catalyst soluble in the solvent, such as besozoyl peroxide, lauryl peroxide, azobisisobutyronitrile, t-butyl peroxide, etc. is added to the solvent, the releasability will be further enhanced.

なお、ギ酸は本発明の必須成分ではない。しかし、これ
の使用を不可とするものではなく、本発明の剥離液によ
りギ酸の有機溶剤に対する相溶性が大になり、剥離性が
より大になる。添加量は大体0.1〜20%が適当であ
る。
Note that formic acid is not an essential component of the present invention. However, this does not preclude its use, and the stripping solution of the present invention increases the compatibility of formic acid with organic solvents, resulting in greater stripping properties. The appropriate amount to add is approximately 0.1 to 20%.

上記剥離液による処理方法は、公知のものと同様に、容
器に剥離液を満たし、これに塗膜を有する金属等の素材
を浸漬することなど実施すれば良い。
The above-mentioned treatment method using the stripping solution may be carried out in the same manner as known methods, such as filling a container with the stripping solution and immersing a material such as metal having a coating film therein.

素材は金属が一般的であるが、セラミックス、本発明の
剥離液で剥離した時、実質上塗膜のみが剥する素材にも
適用できる。
The material is generally metal, but it can also be applied to ceramics, a material from which only the paint film is substantially removed when removed with the stripping solution of the present invention.

(発明の効果) 上記本発明によれば、従来法に比し、著しく短時間で強
固な架橋塗膜を確実に剥離することができ、しかも長時
間の処理によっても性能の低下が少なく、安定した剥離
性能を発揮することができるという優れた効果が得られ
る。
(Effects of the Invention) According to the present invention, it is possible to reliably remove a strong crosslinked coating film in a significantly shorter time than with conventional methods, and there is little deterioration in performance even with long-term treatment, resulting in stable The excellent effect of being able to exhibit excellent peeling performance can be obtained.

実施例1 弗酸のオクチルアミン塩6部メチレンクロライド94部
からなる剥離液に水を加えて約5cmの水層を設けて、
上層が水層、下層が剥離液層からなる複合層を作る。こ
れを約35°に熱する。
Example 1 Water was added to a stripping solution consisting of 6 parts of octylamine salt of hydrofluoric acid and 94 parts of methylene chloride to form a water layer of about 5 cm.
Create a composite layer consisting of an upper layer of water and a lower layer of stripping liquid. Heat this to about 35°.

次に架橋塗膜として約10ミクロン厚のアクリルメラミ
ンレジン電着塗膜を有するアルマイトサッシを前記剥離
液に浸漬した後水洗して清浄にした。塗装品は2分で完
全に剥離した。
Next, an alumite sash having an electrodeposited acrylic melamine resin coating film with a thickness of about 10 microns as a crosslinked coating film was immersed in the stripping solution, and then washed with water to clean it. The painted product was completely peeled off in 2 minutes.

次いで前記条件を持続させて5日間放置し、適宜水を加
えて、約5cmの水層を保持させた。
Next, the above conditions were maintained for 5 days, and water was added as appropriate to maintain a water layer of about 5 cm.

次いで、前記のとおり、塗装品を浸漬したところ、2分
で完全に剥離した。
Then, as described above, the coated product was immersed, and it was completely peeled off in 2 minutes.

更に同様に、5日間放置し、3回目の剥離したところ、
2分で完全に剥離した。
Similarly, after leaving it for 5 days and peeling it off for the third time,
It was completely peeled off in 2 minutes.

比較のため、弗酸のオクチルアミン塩の代りに弗化アン
モニウム又はギ酸とし、液温は25℃にした他は全く同
一にしてテストした。
For comparison, tests were conducted under the same conditions except that ammonium fluoride or formic acid was used instead of the octylamine salt of hydrofluoric acid and the liquid temperature was 25°C.

これは、いずれも約5分で完全に剥離したが、2回目は
30分浸漬しても殆ど剥離しなかつた。
In both cases, it completely peeled off in about 5 minutes, but almost no peeling occurred even after 30 minutes of immersion the second time.

3回目は全く剥離しなかつた。The third time, it did not peel off at all.

従って、本発明法は従来法に比し、極めて優れており、
問題にならなかった。
Therefore, the method of the present invention is extremely superior to the conventional method,
It wasn't a problem.

実施例2 弗酸のトリブチルアミン塩5部メチレンクロライド90
部トリクロルエチレン5部からなる剥離液を作る。
Example 2 Tributylamine salt of hydrofluoric acid 5 parts methylene chloride 90
A stripping solution consisting of 5 parts trichlorethylene is prepared.

次に架橋塗膜として約10ミクロン厚のアクリルメラミ
ンレジン電着塗膜を有するアルマイトサッシを浸漬した
ところ、2分で完全に剥離した。
Next, an alumite sash having an electrodeposited acrylic melamine resin coating with a thickness of about 10 microns as a crosslinked coating was immersed, and it was completely peeled off in 2 minutes.

この剥離操作を24時間繰り返し行ったが、剥離に要す
る処理時間は操作開始時と終了時で全く差がなかった。
This peeling operation was repeated for 24 hours, but there was no difference in the processing time required for peeling between the start and end of the operation.

比較のため、弗酸のトリブチルアミンの代りにギ酸とし
た他は全く同一にしてテストした。
For comparison, the same test was conducted except that formic acid was used instead of tributylamine in hydrofluoric acid.

その結果は、24時間剥離開始時で35分間の浸漬を要
し、終了時では38分間の浸漬を要した。
The results showed that 35 minutes of immersion was required at the beginning of the 24-hour peeling, and 38 minutes of immersion was required at the end of the 24-hour peeling.

作業中の剥離液の減少は溶剤を加えて調節した。The decrease in stripping solution during operation was controlled by adding a solvent.

従って、本発明によれば、従来の行18倍の剥離性能を
有していることがわかる。
Therefore, it can be seen that according to the present invention, the peeling performance is 18 times higher than that of the conventional row.

Claims (1)

【特許請求の範囲】 1、塗膜を有する素材を、弗酸のC_2〜C_1_6の
アミン塩を含有する剥離液で処理、特に加熱処理するこ
とを特徴とする塗膜剥離法。 2、塗膜を有する素材を、弗酸のC_2〜C_1_6の
アミン塩と水より比重の大きい溶剤からなる剥離液の上
部に水層を設けた複合液中び浸漬処理、特に加熱処理す
ることを特徴とする塗膜剥離法。
[Scope of Claims] 1. A method for removing a coating film, which comprises treating a material having a coating film with a stripping solution containing an amine salt of C_2 to C_1_6 of hydrofluoric acid, particularly heat-treating the material. 2. The material with the coating film is immersed in a composite solution consisting of a C_2 to C_1_6 amine salt of hydrofluoric acid and a solvent with a higher specific gravity than water, with an aqueous layer on top, and in particular heat treatment. Characteristic paint film removal method.
JP31105088A 1988-12-09 1988-12-09 Method for peeling coating film Pending JPH02157067A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP31105088A JPH02157067A (en) 1988-12-09 1988-12-09 Method for peeling coating film

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP31105088A JPH02157067A (en) 1988-12-09 1988-12-09 Method for peeling coating film

Publications (1)

Publication Number Publication Date
JPH02157067A true JPH02157067A (en) 1990-06-15

Family

ID=18012506

Family Applications (1)

Application Number Title Priority Date Filing Date
JP31105088A Pending JPH02157067A (en) 1988-12-09 1988-12-09 Method for peeling coating film

Country Status (1)

Country Link
JP (1) JPH02157067A (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5399202A (en) * 1991-12-19 1995-03-21 Hitachi, Ltd. Resist-peeling liquid and process for peeling a resist using the same
US6250317B1 (en) * 1997-02-12 2001-06-26 Kansai Paint Co. Ltd Method of removal of applied film

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5399202A (en) * 1991-12-19 1995-03-21 Hitachi, Ltd. Resist-peeling liquid and process for peeling a resist using the same
US6250317B1 (en) * 1997-02-12 2001-06-26 Kansai Paint Co. Ltd Method of removal of applied film

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