JPS61162568A - Removal of film - Google Patents

Removal of film

Info

Publication number
JPS61162568A
JPS61162568A JP60001445A JP144585A JPS61162568A JP S61162568 A JPS61162568 A JP S61162568A JP 60001445 A JP60001445 A JP 60001445A JP 144585 A JP144585 A JP 144585A JP S61162568 A JPS61162568 A JP S61162568A
Authority
JP
Japan
Prior art keywords
film
aqueous solution
substrate
temperature
polyfunctional acrylic
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.)
Granted
Application number
JP60001445A
Other languages
Japanese (ja)
Other versions
JP2599902B2 (en
Inventor
Hiroshi Imuda
伊牟田 博
Shozo Hieda
省三 稗田
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.)
Mitsui Petrochemical Industries Ltd
Original Assignee
Mitsui Petrochemical Industries Ltd
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 Petrochemical Industries Ltd filed Critical Mitsui Petrochemical Industries Ltd
Priority to JP60001445A priority Critical patent/JP2599902B2/en
Publication of JPS61162568A publication Critical patent/JPS61162568A/en
Application granted granted Critical
Publication of JP2599902B2 publication Critical patent/JP2599902B2/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

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  • Application Of Or Painting With Fluid Materials (AREA)
  • Coating Of Shaped Articles Made Of Macromolecular Substances (AREA)
  • Treatments Of Macromolecular Shaped Articles (AREA)
  • Paints Or Removers (AREA)

Abstract

PURPOSE:To accomplish the titled removal by immersing into an aqueous alkali solution of specific concentration a base body having an its surface multifunctional acrylic cured film to perfectly eliminate said film without damaging the body, thus leading to giving coating film entirely similar to that of new article on coating again. CONSTITUTION:A base body having an its surface multifunctional acrylic cured film is immersed into an aqueous alkali solution of a concentration >=5wt% (pref. 10-30wt%) at, for example, 50-80 deg.C (e.g. derived from LiOH, NaOH, KOH, Mg(OH)2, or Ca(OH)2), thus accomplishing the separation of the film from the body.

Description

【発明の詳細な説明】[Detailed description of the invention]

〔産業上の利用分野〕 本発明は、多官能アクリル系の硬化被膜を表面に有して
いる基体において、たとえば綺麗な硬化被膜の形成に失
敗し硬化被膜の再形成を行いたい時に、一度形成した硬
化被膜を基体より除去し、再度被膜形成を行う場合に適
用できる硬化被膜の除去方法に関する。 〔従来の技術〕 一般に、熱可塑性樹脂、熱硬化性樹脂などの成形体は、
金属製品、ガラス製品などにくらべて軽量で耐衝撃性に
優れているばかりでなく、安価で成形加工が容易である
などの種々の利点を有しており、自動車、オートバイ。 家庭用電化製品1日用雑貨品、その多の多くの分野にお
いて、これらの材質に代わって広く使用されている。し
かし、これらの樹脂などの成形体は金属やガラス等にく
らべて表面硬度が低く、引掻きゃ摩擦に対しても弱いた
めに表面に傷が生じ易いという欠点がある0たとえば、
成形体の部品の取付作業または輸送作業あるいは製品の
使用中に接触、衝突、引掻きなどにより表面に損傷を受
易いなどの表面特性に欠点があるためにこれらの成形体
の利用が著しく制限されている。 このような樹脂などの成形体基本表面の前述の欠点を改
善する方法として多くの提案がなされており、その−例
として1分子中に2つ以上のCメタ)アクリロイル基を
持つ多官能アクリル化合物を表面に塗布したのち、熱ま
たは光によって架橋させ、硬い被膜を形成させる方法が
知られている。 ところで、前記の方法を実際に工業的規模で適用すると
、多官能アクリル化合物を成形体基本に塗布する際に、
たとえば空気中に浮遊している粉塵などが塗装表面に紛
れ込み、硬化被膜に微小な空孔や突起
[Industrial Application Field] The present invention is applicable to a substrate having a polyfunctional acrylic cured film on its surface, for example, when the formation of a beautiful cured film fails and it is desired to re-form the cured film. The present invention relates to a method for removing a cured film that can be applied when the cured film is removed from a substrate and the film is formed again. [Prior art] Generally, molded bodies of thermoplastic resin, thermosetting resin, etc.
Compared to metal products, glass products, etc., it is not only lightweight and has excellent impact resistance, but also has various advantages such as being cheaper and easier to mold. It is widely used in place of these materials in many fields such as household electrical appliances and daily necessities. However, molded bodies made of these resins have lower surface hardness than metals, glass, etc., and are weak against scratches and friction, so they have the disadvantage of being easily scratched on the surface.For example,
The use of these molded bodies is severely limited due to defects in their surface properties, such as susceptibility to surface damage due to contact, collision, scratching, etc., during installation or transportation of molded parts, or during use of the product. There is. Many proposals have been made to improve the above-mentioned drawbacks of the basic surface of molded products such as resins, and one example is a polyfunctional acrylic compound having two or more C meth)acryloyl groups in one molecule. There is a known method in which a hard film is formed by applying a material to a surface and then crosslinking it with heat or light. By the way, when the above method is actually applied on an industrial scale, when applying a polyfunctional acrylic compound to a molded body,
For example, dust floating in the air can get into the painted surface, causing minute holes and protrusions in the hardened film.

【所謂プツ)が発
生して、製品価値を無くしてしまうケースがしばしば生
じる。さらに別には、製品を使用中に何かの弾みで表面
に傷が付いた場合、補修してもとにもどすことが消費者
側から強い要望として存在する。従来、このような場合
に対処する手段としては、塗装置−直す部分を研摩して
再塗装する方法、傷口部分上にそのまま再塗装する方法
、硬化被膜を溶解する特殊溶剤を用いて被膜を溶解除去
したのも再塗装する方法が知られている。しかし、第1
の方法は、被膜が一般塗料の被膜に比べて非常に硬いた
め、均一な研摩が行い難く、シかも残留している古い被
膜上に塗布してできた新しい被膜の密着性も劣る。第2
の方法は、上記の如く重ね塗り被膜の密着性が悪いうえ
、厚肉となった被膜の物性低下の問題がある。第5の方
法は、溶剤によって基本である合成樹脂自身が侵されて
しまうという問題がある。 〔発明が解決しようとする問題点〕 本発明者らは1以上の実情を踏まえ、多官能アクリル系
の硬化被膜を、基本を傷めることなく完全に除去するこ
とができ、かつ除去後に再塗装しても新品に塗装した場
合と何ら変わりないような除去表面が得られる除去方法
がないか研究を重ねた。 〔問題点を解決するための手段〕 すなわち、本発明は表面に多官能アクリル系硬化被膜を
有する基体を、室温以上で基体が変形する温度より低い
温度範囲にある濃度5%以上のアルカリ水溶液中に浸漬
して、硬化被膜と基体とを分離することを特徴とする被
膜の除去方法に関する。 〔作 用〕 本発明は、多官能アクリル系硬化被膜を基本から除去す
るために、含浸などの手段によって特定濃度のアルカリ
水溶液と特¥温度で接触させるのであるが斯様な簡単な
手段によって、従来剥離が困難視されていた多官能アク
リル系の硬化被膜を綺麗に除去できることは実に驚くべ
きことである。 すなわち、本発明の方法を適用する多官能アクリル系硬
化被膜は、同じような表面保護作用を示すシリコン系硬
化被膜と異なり、耐薬品性(耐アルカリ性]が優れてい
ると認識されており、事実各種報告もその点が強調され
ている。たとえば雑誌「塗装と塗料」塗料出版社発行、
A357゜P59〜48には、低濃度の水酸化す) I
Jウム水溶液に4時間部分接触させても硬化被膜に異常
がなかったという記載がある。同様の報告はこの他にも
「高分子加工J@32巻5号P5ろ〜59、 [日化協
月報J  1983年4月号pis〜26および「工業
材料」第50巻4号P68〜72などにも見られ、いず
れも多官能アクリル系の硬化被膜は耐薬品性が良いこと
を支持している。このように、従来の当業者間では1本
発明の如く特定温度下で特定濃度のアルカリ水溶液によ
って多官能アクリル系硬化被膜をいとも簡単に溶解除去
できるとは予想もし得ないことであり、ましてや除去さ
れた基体面上に再塗装すると、再び新品同様の硬化被膜
が形成されることが可能であるとは全く予期し得なかっ
たのである。 本発明の方法を適用し得る多官能アクリル系硬化被膜を
形成する塗料は、1分子中に2つ以上の(メタ)アクリ
ロイル基をもつ化合物を主体にするものであれば如何な
るものでもよく、とくに制限されるものではない。この
ような塗料の例はたとえば前掲した各文献の記載のもの
のほか、特許出願公告46−16091.51−286
77.55−45553.54−1742.56−44
011.特許出願公開49−”+0466.50−11
0477.52−126474.53−102936.
54−30466.54−62269.54−8398
5.54−134795.59−20515.59−2
5840.59−30810.59−53511.59
−16115.59−41566.59−56462.
59−58035.59−6641 Q、59−664
62.59−68317.59−68375.59−7
1535.59−78242.59−78245.59
−80472.59−81563.5 ’?−8492
6,59−84952,59−86631,59−86
666,59−86667,59−86661L 59
−89531.59−89332.59−89367.
59−93715.59−95755.59−9811
5.59−124961の各公報に開示されているもの
などを1例として挙げることができる。 前記の多官能アクリル系の塗料を塗装する基体は、金属
、ガラス、セラミックスなどの無機物、合成樹脂成形体
などの有櫛物等であり、室温以上のアルカリ水溶液に侵
されないものであれば如何なるものでもよい。とくに従
来剥離除去が困難視されていた熱可塑性樹脂や熱硬化性
樹脂などの合成樹脂成形体は、本発明の方法によって簡
単に除去できる。合成樹脂の1例としては、ポリメチル
メタクリレート、ポリカーボネート、ポリエチレン、ポ
リプロピレン、ポリ4−メチルペンテン−1などを承げ
ることができるが、何もこれらの樹脂に限定されるもの
ではない。アルカリ水溶液は、アルカリ金属またはアル
カリ土類金属の水酸化物の水溶液であり、たとえば水酸
化リチウム、水酸化ナトリウム、水酸化カリウム、水酸
化マグネシウム、水酸化カルシウムなどの水溶液を挙げ
ることができる。水溶液の濃度は少なくとも5(重量2
%以上であり、作業上の取扱い性及び安全性の面からは
5〜30%、とくに工業上の連続生産性の面からは10
〜20%が好ましい。5%未満、とくに10%未満の濃
度であると、硬化被膜の溶解剥離に時間がかかりすぎ、
生産性が低下する。アルカリ水溶液の温度は、室温以上
であって基体が変形する温度よりも低い温度範囲であれ
ばよい。しかし、温度が100℃を越えると加圧下に作
業をしなくてはならないので、好ましくは100”C未
満、とくには50〜80’C5更には60〜75℃の範
囲が安全性。 取扱い性に優れかつ基本−とくに合成樹脂の基体に対し
て影響がないので好ましい。室温よりも低い温度である
と、硬化被膜の溶解剥離に時間がかかりすぎ、事実上全
く溶解しないのと同じになる。 基本上の多官能アクリル系硬化被膜を除去するには基体
ごと前記のアルカリ水溶液中に浸清し、水溶液の温度を
前記の温度範囲、好ましくは50〜80”C1とくに6
0〜75℃の範囲内になるように一定に保ち続け、基本
上の多官能アクリル系硬化被膜を溶解剥離して除去する
。含浸時間はとくに制限がなくて、被膜が完全に除去さ
れるまでであるが、水溶液の温度が50″C以上であれ
ば多くが2時間以内とくに1時間以内で除去可能である
。 硬化被膜を除去されたX木は、必要に応じ再塗装されて
硬化被膜を再形成15てもよく、この場合再形成の硬化
被膜は、#r品に形成、させた硬化被膜と比べて何らそ
の性能上の差違はない。 〔実施例〕 以下に本発明の好適な例を実施例として示すが、本発明
はとくに断わりのない限り何らこれらの例に限定される
ものではない。 実施例1〜5および比較例1〜2 多官能アクリルモノマーとしてトリス(アクロイルオキ
シエチル)イソシアヌレートを主成分とし、これと光重
合開始剤、無機充填材および有機溶剤とから紫外線硬化
型多官能アクリル系被覆組成物を作製した。 一方、ポリプロピレン〔三井石油化学工業KK製、商品
名、三井石油化学ポリプロ、r、140r群青を1.2
鳴入れて青色に着色したもの)以下、ppと略称〕から
作製した射出角板C厚み2mm)を1゜1.1− トリ
クロルエタン蒸気に30秒間さらし、その後室温下1分
乾燥した後に各種被覆用組成物をエアースプレー(吐出
圧5kg7cm )にて塗布し、5分間セツティングを
行った後に80℃で5分間乾燥を行った。ついでこの試
験片を3KW高圧水銀灯下。 151の距離で紫外線を約50秒間照射し、外被膜を硬
化させた。 この様にして被覆した射出成形角板を表1に示す剥離液
に50分間浸漬し、被膜層の剥離状況を観察した。結果
を表1に示す。尚、表1には後述する実施例6〜8の結
果も併記する。 実施例6 ボリ4−メチル−1−ペンテンC三井石油化学製、商品
名: TPX■MX−004,以下TPXと略称)の2
mm厚の射出成形角板を無水マレイン酸変性EPR(無
水マレイン酸含量ニア、7+重量)%〕の15 g/1
28度のトルエン溶液中に10秒間浸漬し、プライマー
処理を行った。室温で5分間放置後、実施例1に記載の
方法により外被膜層を形成した。 この様にして被覆した射出成形角板を70℃に保った1
5%の水酸化す) IJウム水溶液に50分間浸漬した
ところ、被覆膜は完全に溶解除去された。 実施例7〜8 表面被覆ポリマーシートとして、多官能アクリル系紫外
線硬化型ハードコート被覆を行ったポリカーボネートc
以下、PCと略称】シート(三菱レイヨン製、商品名:
ダイアライト■AR)およびポリメチルメタアクリレー
トc以下、PMMAと略称)シート(三菱レイヨン製、
商品名ニアクリライト■AR)より試験片を切り出し、
実施例1に記載された方法により水酸化ナトリウム水溶
液に浸漬したところ被膜層はいずれも完全に溶解除去さ
れた。 表1(続き) 実施例9 実施例1で被膜を除去した基材に、再度実施例1と同様
にして硬化被膜を形成した。得られた被膜の物性を新品
の基材に形成した硬化被覆と比較して表2に示す。 表    2 *1 JIS  K  5400−1979中のゴバン
目テストに圀じて行った。 *1 JIS  K  5400−1979中の60度
鏡面光沢度に準じて行った。 〔発明の効果〕 以と述べた始く、本発明の方法によれば(1)従来剥離
が困睡とされていた多官能アクリル系硬化被膜を除去す
ることができる、 (2)剥離対象の硬化被膜を確実かつ完全に除去するこ
とかできる、 (3)基体には全く影響を与えない。 (4)アルカリ水溶液中に浸漬するだけなので作業が簡
単である、 (5)硬化被膜除宏後の基本表面上は綺麗であり、した
がって再塗装後の硬化被膜の性能も良い、といった優れ
た効果を示す。
[So-called puttu] often occurs and the value of the product is lost. Furthermore, there is a strong demand from consumers to repair and restore the product to its original condition if the surface of the product is damaged by some force during use. Conventionally, methods for dealing with such cases include methods such as sanding and repainting the area where the paint has been replaced, methods of repainting directly on the scratched area, and methods of dissolving the film using a special solvent that dissolves the hardened film. There is a known method of repainting the removed part. However, the first
In this method, the film is much harder than that of ordinary paints, so it is difficult to polish uniformly, and the adhesion of the new film formed by applying it over the old film that remains is also poor. Second
As mentioned above, this method has problems in that the adhesion of the overcoated film is poor and the physical properties of the thick film deteriorate. The fifth method has a problem in that the basic synthetic resin itself is attacked by the solvent. [Problems to be Solved by the Invention] Based on one or more actual circumstances, the present inventors have developed a method that allows a polyfunctional acrylic hardened film to be completely removed without damaging the base, and that can be repainted after removal. We conducted repeated research to find a removal method that would yield a surface that would be no different from a newly painted surface. [Means for Solving the Problems] That is, the present invention provides a substrate having a polyfunctional acrylic cured coating on its surface in an alkaline aqueous solution with a concentration of 5% or more at a temperature range above room temperature but below the temperature at which the substrate deforms. The present invention relates to a method for removing a coating, which comprises separating the cured coating from the substrate by immersing the substrate in water. [Function] In the present invention, in order to remove the polyfunctional acrylic cured coating from the base, it is brought into contact with an alkaline aqueous solution of a specific concentration at a specific temperature by means such as impregnation. It is truly surprising that a polyfunctional acrylic cured film, which has traditionally been considered difficult to remove, can be removed cleanly. In other words, the polyfunctional acrylic cured coating to which the method of the present invention is applied is recognized to have excellent chemical resistance (alkali resistance), unlike silicone cured coatings that exhibit a similar surface protection effect. Various reports also emphasize this point. For example, the magazine "Painting and Paints" published by Paint Publishing Co., Ltd.
A357゜P59-48 contains a low concentration of hydroxide) I
There is a statement that there was no abnormality in the cured film even after partial contact with a Jium aqueous solution for 4 hours. Similar reports are also available in "Polymer Processing J @ Vol. 32 No. 5 P5-59, [JCIA Monthly Report J April 1983 issue pis-26 and "Industrial Materials" Vol. 50 No. 4 P68-72 Both of these studies support the fact that polyfunctional acrylic cured coatings have good chemical resistance. As described above, it is impossible for those skilled in the art to predict that a polyfunctional acrylic cured coating could be so easily dissolved and removed using an alkaline aqueous solution of a specific concentration at a specific temperature as in the present invention, and even more so. It was completely unexpected that a cured film as good as new could be formed again by recoating on the surface of the substrate. The coating material forming a polyfunctional acrylic cured film to which the method of the present invention can be applied may be any coating material as long as it is mainly composed of a compound having two or more (meth)acryloyl groups in one molecule. There are no restrictions. Examples of such paints include those described in the above-mentioned documents, as well as patent application publication No. 46-16091.51-286.
77.55-45553.54-1742.56-44
011. Patent application publication 49-”+0466.50-11
0477.52-126474.53-102936.
54-30466.54-62269.54-8398
5.54-134795.59-20515.59-2
5840.59-30810.59-53511.59
-16115.59-41566.59-56462.
59-58035.59-6641 Q, 59-664
62.59-68317.59-68375.59-7
1535.59-78242.59-78245.59
-80472.59-81563.5'? -8492
6, 59-84952, 59-86631, 59-86
666, 59-86667, 59-86661L 59
-89531.59-89332.59-89367.
59-93715.59-95755.59-9811
Examples include those disclosed in each publication of No. 5.59-124961. The substrate to which the polyfunctional acrylic paint is applied may be any inorganic material such as metal, glass, or ceramics, or a combed material such as a synthetic resin molding, as long as it is not attacked by an alkaline aqueous solution at room temperature or above. But that's fine. In particular, synthetic resin molded bodies such as thermoplastic resins and thermosetting resins, which have conventionally been considered difficult to peel and remove, can be easily removed by the method of the present invention. Examples of synthetic resins include polymethyl methacrylate, polycarbonate, polyethylene, polypropylene, poly-4-methylpentene-1, etc., but are not limited to these resins. The alkaline aqueous solution is an aqueous solution of an alkali metal or alkaline earth metal hydroxide, and examples thereof include aqueous solutions of lithium hydroxide, sodium hydroxide, potassium hydroxide, magnesium hydroxide, calcium hydroxide, and the like. The concentration of the aqueous solution is at least 5 (weight 2
% or more, from 5 to 30% in terms of workability and safety, and in particular 10% in terms of industrial continuous productivity.
~20% is preferred. If the concentration is less than 5%, especially less than 10%, it will take too long for the cured film to dissolve and peel off.
Productivity decreases. The temperature of the alkaline aqueous solution may be within a range of room temperature or higher and lower than the temperature at which the substrate deforms. However, if the temperature exceeds 100°C, the work must be carried out under pressure, so it is safe to operate preferably below 100'C, especially in the range of 50 to 80'C5, and even 60 to 75°C. Excellent and Basic - This is particularly preferred as it has no effect on synthetic resin substrates.If the temperature is lower than room temperature, it will take too long for the cured film to dissolve and peel off, which is practically the same as not dissolving at all.Basics To remove the polyfunctional acrylic cured coating, the substrate is immersed in the alkali aqueous solution mentioned above, and the temperature of the aqueous solution is adjusted to the above temperature range, preferably 50 to 80" C1, especially 6
The temperature is kept constant within the range of 0 to 75°C, and the basic polyfunctional acrylic cured coating is removed by dissolving and peeling. There is no particular restriction on the impregnation time, and it is until the film is completely removed, but if the temperature of the aqueous solution is 50"C or higher, most of the time can be removed within 2 hours, especially within 1 hour. The removed X wood may be repainted as necessary to re-form the hardened film15, and in this case, the re-formed hardened film has no performance improvement compared to the hardened film formed on the #r product. There is no difference. [Example] Preferred examples of the present invention are shown below as Examples, but the present invention is not limited to these examples in any way unless otherwise specified. Examples 1 to 5 and Comparative Examples 1 to 2 A UV-curable polyfunctional acrylic coating composition was prepared from tris(acroyloxyethyl)isocyanurate as the main component as a polyfunctional acrylic monomer, a photopolymerization initiator, an inorganic filler, and an organic solvent. On the other hand, polypropylene [manufactured by Mitsui Petrochemical Industries KK, trade name, Mitsui Petrochemical Polypro, R, 140r Gunjo] was mixed with 1.2
An injection square plate C (thickness: 2 mm) made from 1°1.1-trichloroethane vapor (hereinafter abbreviated as PP) was exposed to 1°1.1-trichloroethane vapor for 30 seconds, then dried for 1 minute at room temperature, and then coated with various coatings. The composition was applied by air spray (discharge pressure: 5 kg, 7 cm), and after setting for 5 minutes, it was dried at 80° C. for 5 minutes. Next, this test piece was placed under a 3KW high-pressure mercury lamp. The outer coating was cured by irradiating it with ultraviolet light for about 50 seconds at a distance of 151 mm. The injection molded square plate coated in this manner was immersed in the stripping solution shown in Table 1 for 50 minutes, and the peeling status of the coating layer was observed. The results are shown in Table 1. Note that Table 1 also shows the results of Examples 6 to 8, which will be described later. Example 6 Poly-4-methyl-1-pentene C manufactured by Mitsui Petrochemicals, product name: TPX MX-004 (hereinafter abbreviated as TPX)-2
A mm-thick injection-molded square plate was prepared with 15 g/1 of maleic anhydride-modified EPR (maleic anhydride content near, 7 + weight)%].
Primer treatment was performed by immersing it in a toluene solution at 28 degrees for 10 seconds. After standing at room temperature for 5 minutes, an outer coating layer was formed by the method described in Example 1. The injection molded square plate coated in this way was kept at 70°C.
When it was immersed in a 5% hydroxide aqueous solution for 50 minutes, the coating film was completely dissolved and removed. Examples 7-8 Polycarbonate c coated with a polyfunctional acrylic ultraviolet curable hard coat as a surface-coated polymer sheet
Hereinafter abbreviated as PC] Sheet (manufactured by Mitsubishi Rayon, product name:
Dialite ■AR) and polymethyl methacrylate c (hereinafter abbreviated as PMMA) sheet (manufactured by Mitsubishi Rayon,
Cut out a test piece from the product name Niacrylite ■AR).
When immersed in an aqueous sodium hydroxide solution using the method described in Example 1, all of the coating layers were completely dissolved and removed. Table 1 (Continued) Example 9 A cured film was again formed in the same manner as in Example 1 on the base material from which the film had been removed in Example 1. The physical properties of the resulting coating are shown in Table 2 in comparison with those of a cured coating formed on a new substrate. Table 2 *1 This was carried out in conjunction with the burrow test in JIS K 5400-1979. *1 Performed according to 60 degree specular gloss in JIS K 5400-1979. [Effects of the Invention] As described above, according to the method of the present invention, (1) it is possible to remove a polyfunctional acrylic cured film, which has conventionally been difficult to remove; (2) it is possible to remove the The cured film can be removed reliably and completely. (3) It does not affect the substrate at all. (4) It is easy to work as it only needs to be immersed in an alkaline aqueous solution. (5) The basic surface after removal of the cured film is clean, and therefore the performance of the cured film after repainting is also good. shows.

Claims (4)

【特許請求の範囲】[Claims] (1)表面に多官能アクリル系硬化被膜を有する基体を
、室温以上で基体が変形する温度より低い温度範囲にあ
る濃度5%以上のアルカリ水溶液中に浸漬して、硬化被
膜と基体とを分離することを特徴とする被膜の除去方法
(1) Separate the cured film from the substrate by immersing the substrate with a polyfunctional acrylic cured coating on the surface in an alkaline aqueous solution with a concentration of 5% or more at a temperature range above room temperature but below the temperature at which the substrate deforms. A film removal method characterized by:
(2)アルカリ水溶液の温度が50〜80℃である特許
請求の範囲第1項記載の被膜の除去方法。
(2) The method for removing a film according to claim 1, wherein the temperature of the alkaline aqueous solution is 50 to 80°C.
(3)アルカリ水溶液の濃度が10〜30%である特許
請求の範囲第1項または第2項に記載の被膜の除去方法
(3) The method for removing a film according to claim 1 or 2, wherein the concentration of the alkaline aqueous solution is 10 to 30%.
(4)アルカリ水溶液が水酸化リチウム、水酸化ナトリ
ウム、水酸化カリウム、水酸化マグネシウム、水酸化カ
ルシウムの水溶液から選ばれる特許請求の範囲第1項な
いし第5項のいずれかに記載の被膜の除去方法。
(4) Removal of the film according to any one of claims 1 to 5, wherein the alkaline aqueous solution is selected from aqueous solutions of lithium hydroxide, sodium hydroxide, potassium hydroxide, magnesium hydroxide, and calcium hydroxide. Method.
JP60001445A 1985-01-10 1985-01-10 Removal method of cured film Expired - Lifetime JP2599902B2 (en)

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Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB2271356A (en) * 1992-09-25 1994-04-13 Nissan Motor Method of removing coating films
JP2015077541A (en) * 2013-10-16 2015-04-23 地方独立行政法人山口県産業技術センター Coating film removal method and coating film removal device

Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5226549A (en) * 1975-08-26 1977-02-28 Adeka Argus Chem Co Ltd Halogen-containing resin compositions
JPS56129273A (en) * 1980-02-15 1981-10-09 Sterling Drug Inc Coating grade aqueous composition for peeling paint
JPS57163236A (en) * 1981-03-31 1982-10-07 Hitachi Chem Co Ltd Peeling solution for use in photocured film

Patent Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5226549A (en) * 1975-08-26 1977-02-28 Adeka Argus Chem Co Ltd Halogen-containing resin compositions
JPS56129273A (en) * 1980-02-15 1981-10-09 Sterling Drug Inc Coating grade aqueous composition for peeling paint
JPS57163236A (en) * 1981-03-31 1982-10-07 Hitachi Chem Co Ltd Peeling solution for use in photocured film

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB2271356A (en) * 1992-09-25 1994-04-13 Nissan Motor Method of removing coating films
GB2271356B (en) * 1992-09-25 1996-01-31 Nissan Motor Method of removing coating films from resin substrates
US5542982A (en) * 1992-09-25 1996-08-06 Nissan Motor Co., Ltd. Method of removing coating films
DE4332642B4 (en) * 1992-09-25 2004-07-29 Mitsui Chemicals, Inc. Process for removing coating films
JP2015077541A (en) * 2013-10-16 2015-04-23 地方独立行政法人山口県産業技術センター Coating film removal method and coating film removal device

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