JPH059419A - Agent and process for releasing and removing coating resin film - Google Patents

Agent and process for releasing and removing coating resin film

Info

Publication number
JPH059419A
JPH059419A JP3185834A JP18583491A JPH059419A JP H059419 A JPH059419 A JP H059419A JP 3185834 A JP3185834 A JP 3185834A JP 18583491 A JP18583491 A JP 18583491A JP H059419 A JPH059419 A JP H059419A
Authority
JP
Japan
Prior art keywords
resin
peeling
coating
compound
agent
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
JP3185834A
Other languages
Japanese (ja)
Other versions
JP2924323B2 (en
Inventor
Kaoru Asakawa
薫 浅川
Atsushi Kato
淳 加藤
Hiroki Nagayama
啓樹 永山
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.)
Nissan Motor Co Ltd
Original Assignee
Nissan Motor Co 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 Nissan Motor Co Ltd filed Critical Nissan Motor Co Ltd
Priority to JP3185834A priority Critical patent/JP2924323B2/en
Priority to US07/856,794 priority patent/US5256210A/en
Priority to GB9226893A priority patent/GB2273715B/en
Priority claimed from GB9226893A external-priority patent/GB2273715B/en
Priority to DE4244355A priority patent/DE4244355C2/en
Publication of JPH059419A publication Critical patent/JPH059419A/en
Application granted granted Critical
Publication of JP2924323B2 publication Critical patent/JP2924323B2/en
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

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  • Paints Or Removers (AREA)

Abstract

PURPOSE:To provide an agent for releasing and removing a coating resin film which has a performance of effectively removing a coating film, good workability and high environmental safety, and a process for releasing and removing a coating resin film. CONSTITUTION:An agent for releasing and removing a coating resin film comprising 10-90wt.% compound A having an unsaturation between a carbon atom and an atom of a different kind, such as an aprotic solvent, an imide or a ketone, and 10-90wt.% compound B comprising an at least monohydric alcohol having a boiling point of 250 deg.C or below and being normally liquid or its derivative. This agent is sprayed onto or applied to a coated part at 50-150 deg.C or this part is immersed in the agent to release and remove the resin film from the part.

Description

【発明の詳細な説明】Detailed Description of the Invention

【0001】[0001]

【産業上の利用分野】樹脂塗装の加工工程、またはリサ
イクル材の前処理工程において、効果的な塗装除去性
能、良好な作業性、高い環境安全性を有する、樹脂部品
の塗装除去剤及び塗装除去法が求められている。この発
明はオゾン層破壊等を引き起こさず、かつ取扱い性に優
れる、樹脂塗膜の剥離除去剤、およびこの剥離除去剤を
使用する樹脂塗膜の剥離除去方法に関するものである。
[Industrial application] Coating removal agents and coating removal for resin parts that have effective coating removal performance, good workability, and high environmental safety in resin coating processing or pretreatment of recycled materials. Law is required. The present invention relates to a resin film peeling and removing agent that does not cause ozone layer destruction and the like and is excellent in handleability, and a resin coating film peeling and removing method using the peeling and removing agent.

【0002】[0002]

【従来の技術】従来の樹脂塗膜の剥離剤としては、クロ
ロペンタフルオロプロパン/1,1ジクロロ−1−トリ
フルオロエタン混合溶剤組成物(特開平2−286795号公
報)およびクロロペンタフルオロプロパン/ジクロロト
リフルオロエタン混合溶剤組成物(特開平2−286796号
公報)等が提示されている。また、発明者らは既に、樹
脂塗装剥離除去剤組成液および除去法(特願平3−8300
9号)にて物理または化学的に塗膜を剥離できる溶剤ま
たは溶液組成を提示した。さらに、塩化メチレンの如き
通常のハロゲン系溶剤あるいは、強アルカリ溶液あるい
は、強酸溶液がよく知られている。
2. Description of the Related Art As conventional stripping agents for resin coatings, chloropentafluoropropane / 1,1 dichloro-1-trifluoroethane mixed solvent composition (JP-A-2-286795) and chloropentafluoropropane / A mixed solvent composition of dichlorotrifluoroethane (JP-A-2-286796) is proposed. In addition, the inventors have already disclosed a resin coating peeling remover composition liquid and a removing method (Japanese Patent Application No. 3-8300).
No. 9) presented a solvent or solution composition that can physically or chemically remove the coating film. Further, a normal halogen-based solvent such as methylene chloride, a strong alkaline solution, or a strong acid solution is well known.

【0003】[0003]

【発明が解決しようとする課題】前記特開平2−286795
号公報および同2−286796号公報に開示されている混合
溶剤組成物は、対油脂洗浄力に優れ、オゾン層破壊の危
険性が低いという特徴を持つ反面、特殊な溶剤を用いる
ため電気部品等の用途に限定されること、かつ、分子鎖
に多数のハロゲン原子(F,C1)を含有するため、環
境衛生上取扱いに注意をようすることなどの問題点があ
った。また通常のハロゲン系溶剤の使用は環境衛生を悪
化させると同時に、オゾン層破壊を引き起こすという問
題があった。強アルカリ溶液、強酸溶液の使用において
も、作業安全性、環境安全上の問題と共に、中和等の後
処理工程が必須であるなどの煩雑さがあった。また、前
記特願平3− 83009号明細書に記載した混合溶剤組成物
は、塗膜樹脂の組成種により塩素化ポリオレフィン等か
ら成るプライマー面の剥離が十分でないものがあった。
プライマー面の剥離が不十分な材料を用いて混練り等を
行った場合、加工機器の接触表面に腐食を引き起こす等
の問題があった。
DISCLOSURE OF THE INVENTION Problems to be Solved by the Invention
The mixed solvent composition disclosed in JP-A No. 2-286796 and JP-A No. 2-286796 has the characteristics that it is excellent in detergency against fats and oils and has a low risk of depleting the ozone layer. However, since the molecular chain contains a large number of halogen atoms (F, C1), there are problems such as being careful in handling in terms of environmental hygiene. In addition, there is a problem that use of a normal halogen-based solvent deteriorates environmental hygiene and, at the same time, causes ozone layer depletion. Even when a strong alkaline solution or a strong acid solution is used, there are problems in work safety and environmental safety, and there are complications such as the necessity of a post-treatment step such as neutralization. Further, in some of the mixed solvent compositions described in the above-mentioned Japanese Patent Application No. 3-83009, the primer surface made of chlorinated polyolefin or the like was not sufficiently peeled off depending on the composition of the coating resin.
When kneading or the like is performed using a material whose peeling of the primer surface is insufficient, there is a problem such as causing corrosion on the contact surface of the processing equipment.

【0004】この発明は従来のこのような問題点に着目
してなされたもので、非プロトン性溶媒、或いはイミン
類またはケトン類などの異種原子間に不飽和結合を有す
る化合物Aを10〜90重量%、好ましくは20〜80重量%
と、沸点が250 ℃以下の常温で液体状態を呈する、一価
以上のアルコール類或いはその誘導体から成る化合物B
を10〜90重量%、好ましくは20〜80重量%から成る剥離
除去剤を50℃〜150℃、好ましくは50〜100 ℃の温度で
樹脂塗装処理樹脂部品に塗布するか、或いは前記剥離除
去剤に上記樹脂部品を浸漬することにより上記問題点を
解決したものである。
The present invention has been made by paying attention to such a conventional problem, and 10 to 90% of a compound A having an unsaturated bond between different atoms such as an aprotic solvent or imines or ketones is used. % By weight, preferably 20-80% by weight
And a compound B consisting of a monohydric or higher alcohol or its derivative, which has a boiling point of 250 ° C. or lower and is in a liquid state at room temperature.
Of 10 to 90% by weight, preferably 20 to 80% by weight, is applied to the resin-coated resin parts at a temperature of 50 ° C to 150 ° C, preferably 50 to 100 ° C. The above-mentioned problems are solved by immersing the above-mentioned resin component in.

【0005】本発明の樹脂塗膜剥離除去剤は、非プロト
ン性溶媒、或いはイミン類またはケトン類などの異種原
子間に不飽和結合を有する化合物Aを10〜90重量%、好
ましくは20〜80重量%と、沸点が250 ℃以下の常温で液
体状態を呈する、一価以上のアルコール類或いはその誘
導体から成る化合物Bを10〜90重量%、好ましくは20〜
80重量%から成ることを特徴とするものである。
The resin coating film peeling / removing agent of the present invention contains 10 to 90% by weight, preferably 20 to 80% by weight of an aprotic solvent or a compound A having an unsaturated bond between different atoms such as imines or ketones. 10 to 90% by weight, preferably 20 to 90% by weight, of the compound B composed of a monohydric or higher alcohol or its derivative, which is in a liquid state at room temperature with a boiling point of 250 ° C or less.
It is characterized by comprising 80% by weight.

【0006】上記異種原子間に不飽和結合を有するか化
合物Aの非プロトン性溶媒としては次式
Is an aprotic solvent of the above compound A having an unsaturated bond between the above-mentioned heteroatoms:

【化1】 〔式中のR1 は水素原子またはメチル基を示し、R2
NH2 基またはN(CH3)2 基を示す] および次式
[Chemical 1] [Wherein R 1 represents a hydrogen atom or a methyl group, and R 2 represents an NH 2 group or an N (CH 3 ) 2 group] and the following formula

【化2】 〔式中のR3 は-C3H6-N(CH3)- 或いは、-C3H6-NH- 或い
は、-N(CH3)-C2H4-N(CH3)- 或いは、-N(CH3)-C2H4-N(C
H3)- を示す] で表されるアミド類、次式
[Chemical 2] [Wherein R 3 is -C 3 H 6 -N (CH 3 )-or -C 3 H 6 -NH- or -N (CH 3 ) -C 2 H 4 -N (CH 3 )-or , -N (CH 3 ) -C 2 H 4 -N (C
H 3 )-], represented by the following formula

【化3】 〔式中のR4 およびR5 はCn H2n+1( n=1 〜4)〕で
表されるスルホキシド類が用いられる。
[Chemical 3] Sulfoxides represented by the formula [R 4 and R 5 in the formula are C n H 2 n + 1 (n = 1 to 4)] are used.

【0007】これらの非プロトン性溶媒としてはホルム
アミド、N,N−ジメチルホルムアミド、N−メチルピ
ロリドン、1,3−ジメチル−2−イミダゾリジノン、
ジメチルスルホキシド等が好ましく用いられる。また上
記化合物Aのケトン類としては次式
These aprotic solvents include formamide, N, N-dimethylformamide, N-methylpyrrolidone, 1,3-dimethyl-2-imidazolidinone,
Dimethyl sulfoxide and the like are preferably used. Further, as the ketones of the above compound A, the following formula

【化4】 〔式中のR6 およびR7 はCn 2n+1 (n =1 〜10) ま
たは芳香族基を示す] で表されるケトン類が用いられ、
この内メチルエチルケトン等が好ましく用いられる。さ
らに上記化合物Aのイミン類としては R8 −N=C=N−R9 (式中のR8 およびR9 はC6 11を示す) で表される
イミン等が用いられる。
[Chemical 4] [Wherein R 6 and R 7 in the formula represent C n H 2n + 1 (n = 1 to 10) or an aromatic group],
Of these, methyl ethyl ketone and the like are preferably used. Further, as the imine of the compound A, an imine represented by R 8 —N═C═N—R 9 (R 8 and R 9 in the formula represent C 6 H 11 ) and the like are used.

【0008】また上記化合物Bとしては、次式 R10−OH 〔式中のR10はCn H2n+1 (n=1 〜10) 又は芳香族基
を示す〕で表されるモノオール類、次式 HO−R11−OH 〔式中のR11はCn H2n (n=1 〜10) 又は芳香族基を
示す〕で表されるジオール類、次式 R12−SH 〔式中のR12はCn H2n+1 (n=1 〜10) 又は芳香族基
を示す〕で表されるチオール類( モノチオール) が用い
られる。
Further, as the compound B, monools represented by the following formula R 10 --OH [wherein R 10 represents C n H 2 n + 1 (n = 1 to 10) or an aromatic group] diols represented by the following formula HO-R 11 -OH [R 11 in the formula have C n H2 n (n = 1 ~10) or an aromatic group], the formula R 12 -SH wherein R 12 of C n H2 n + 1 (n = 1 to 10) or an aromatic group] is used as the thiol (monothiol).

【0009】[0009]

【作用】上記化合物Aは主にプライマー樹脂に拡散/浸
透し、プライマー樹脂の膨潤、膨脹させ、それを剥離せ
しめる。そのため、化合物Aの濃度が10重量%未満の場
合、プライマー樹脂を十分膨潤、膨脹させるに至らず、
塗装が剥離しない。また、化合物Aが90重量%より大き
くなると塗装樹脂の膨潤が不十分で塗装が剥離しない場
合がある。上記塗膜剥離除去剤に対して樹脂塗装樹脂部
品が膨潤した場合、質量変化率が20%未満の場合、塗装
樹脂の膨潤が不十分であり、塗装樹脂を剥離せしめるこ
とができない。一方、上記樹脂塗膜の剥離除去剤は、モ
ノ、ジオール若しくはその誘導体を有する前記化合物B
を10〜90重量%、望ましくは20〜80重量%含有する。化
合物Bは主に塗装樹脂を拡散/浸透し、塗装樹脂を膨
潤、膨脹せしめると共に、化合物Aの拡散/浸透を促進
する。さらに化合物Bは親水性および親油性基を有する
ため、塗装樹脂/プライマー樹脂/樹脂部品の界面から
の上記塗膜剥離除去剤浸透に対する効果もある。
The above-mentioned compound A mainly diffuses / penetrates into the primer resin, swells and swells the primer resin, and separates it. Therefore, when the concentration of the compound A is less than 10% by weight, the primer resin is not sufficiently swollen and expanded,
The paint does not peel off. On the other hand, when the amount of the compound A is more than 90% by weight, the swelling of the coating resin may be insufficient and the coating may not be peeled off. When the resin-coated resin component swells with respect to the coating film peeling remover and the mass change rate is less than 20%, the swelling of the coating resin is insufficient and the coating resin cannot be peeled off. On the other hand, the above-mentioned peeling remover for the resin coating film is the compound B having mono, diol or its derivative.
10 to 90% by weight, preferably 20 to 80% by weight. The compound B mainly diffuses / penetrates the coating resin, swells and expands the coating resin, and promotes the diffusion / permeation of the compound A. Further, since the compound B has hydrophilic and lipophilic groups, it has an effect on the penetration of the above-mentioned coating film peeling / removing agent from the interface of coating resin / primer resin / resin part.

【0010】しかし、炭素連鎖長が10以上の化合物Aを
用いると、沸点が250 ℃を越え、液の粘度も上昇すると
共に、親油性が増加し、水に対する溶解度が著しく低下
し、樹脂剥離除去剤よる塗膜濡れ性および拡散/浸透
性、並びに乾燥工程等の作業性を損なうことから、n−
ドデシルアルコール等は使用に適さない。また、化合物
Bを90重量%より多く使用した場合、プライマー樹脂を
十分に膨潤、膨脹せしめることができず、塗装樹脂が剥
離しないことがある。
However, when the compound A having a carbon chain length of 10 or more is used, the boiling point exceeds 250 ° C., the viscosity of the liquid increases, the lipophilicity increases, the solubility in water decreases remarkably, and the resin peels off. Since the coating film wettability and diffusion / permeability due to the agent impair the workability in the drying step, etc.
Dodecyl alcohol is not suitable for use. Further, when the compound B is used in an amount of more than 90% by weight, the primer resin cannot be sufficiently swollen and expanded, and the coating resin may not be peeled off.

【0011】以上説明してきた本発明の樹脂塗膜の剥離
除去剤はアクリル系、メラミン系或いはウレタン系樹脂
塗料処理樹脂部品の樹脂塗膜の剥離除去に特に好ましく
用いられる。剥離除去は前記の如く剥離除去剤を樹脂塗
料部品に噴霧若しくは塗布するか、或いは剥離除去剤に
樹脂塗装部品を浸漬することにより行うことができる。
The above-described resin film peeling and removing agent of the present invention is particularly preferably used for peeling and removing the resin coating film of the acrylic, melamine or urethane resin coating treated resin parts. The peeling removal can be performed by spraying or applying the peeling remover to the resin paint component as described above, or by immersing the resin coated component in the peeling remover.

【0012】次に本発明を図面により説明する。図1は
樹脂塗装部品の断面を示す図である。塗装表面側から、
塗装樹脂層1、次にプライマー樹脂層2、最下層の樹脂
基材3から構成される。本発明の樹脂塗膜の剥離除去剤
および剥離除去方法を使用し、上記樹脂塗装部品から、
塗装を剥離除去する際の3タイプの剥離機構を図2(a),
(b), (c) に示した。図2(a) は主に化合物Bの作用に
より塗装樹脂層1がプライマー樹脂層2に較べて著しく
膨潤、膨脹し塗装樹脂層1/プライマー樹脂層2の界面
付近4で剥離することを示す。逆に、図2(b) では主に
化合物Aの作用により、プライマー樹脂2が塗装樹脂層
1に比べて、著しく膨潤、膨脹し塗装樹脂層1/プライ
マー樹脂層2またはプライマー樹脂層2/樹脂基材3の
界面付近4で剥離することを示す。次に、図2(c) では
化合物A,B両方の作用により、塗装樹脂層1とプライ
マー樹脂層2が膨潤、膨脹するが硬化度の低いプライマ
ー層2の膨潤が著しく進行してプライマー樹脂層2/樹
脂基材3の界面付近4で剥離するに至ることを示す。
Next, the present invention will be described with reference to the drawings. FIG. 1 is a view showing a cross section of a resin coated component. From the painted surface side,
The coating resin layer 1, then the primer resin layer 2 and the resin base material 3 as the lowermost layer. Using the resin film peeling removal agent and peeling removal method of the present invention, from the resin coated parts,
Fig. 2 (a) shows three types of peeling mechanism for peeling and removing the coating.
Shown in (b) and (c). FIG. 2A shows that the coating resin layer 1 swells and swells remarkably as compared with the primer resin layer 2 due to the action of the compound B, and peels off at the interface vicinity 4 of the coating resin layer 1 / primer resin layer 2. On the contrary, in FIG. 2 (b), the primer resin 2 is significantly swollen and expanded as compared with the coating resin layer 1 mainly due to the action of the compound A, and thus the coating resin layer 1 / primer resin layer 2 or the primer resin layer 2 / resin It shows that peeling occurs near the interface 4 of the base material 3. Next, in FIG. 2 (c), the coating resin layer 1 and the primer resin layer 2 swell due to the action of both the compounds A and B, and the swelling of the primer layer 2 having a low degree of curing progresses remarkably and the primer resin layer 2 2 shows that peeling occurs at the vicinity 4 of the interface of the resin base material 3.

【0013】図2(a), (b), (c) の全剥離機構において
も、塗装樹脂層1、或いはプライマー樹脂層2のいずれ
かが膨潤度(ΔWs)20重量%以上に膨潤した場合に塗
装剥離が観察される。また、上記塗装剥離において、樹
脂基材3の膨潤、膨脹はまったく認められない。尚、膨
潤度(ΔWs)を下記のように定義する。 ΔWs(%) =100(Ws−Wo) /Wo Wo: 塗膜剥離除去剤による膨潤、膨脹前の塗装樹脂層1
或いはプライマー樹脂層2の重量 Ws: 塗膜剥離除去剤による膨潤、膨脹後(温度:50〜 1
50℃、処理時間:15分) の塗装樹脂層1或いはプライマ
ー樹脂層2の重量
2 (a), 2 (b) and 2 (c), when either the coating resin layer 1 or the primer resin layer 2 swells to a swelling degree (ΔWs) of 20% by weight or more. Paint peeling is observed. In addition, the swelling or swelling of the resin base material 3 is not recognized at all in the above-mentioned coating peeling. The degree of swelling (ΔWs) is defined as follows. ΔWs (%) = 100 (Ws−Wo) / Wo Wo: Swelling by the paint remover, coating resin layer 1 before expansion
Alternatively, the weight of the primer resin layer 2 Ws: swelling by the paint removal agent, after swelling (temperature: 50 to 1
Weight of coating resin layer 1 or primer resin layer 2 at 50 ℃, processing time: 15 minutes)

【0014】次に、前記樹脂塗膜の剥離除去剤の使用温
度としては50〜150℃、望ましくは60〜 100℃である。5
0℃より低い使用温度では前記剥離除去剤が塗装樹脂お
よびプライマー樹脂に十分速く、拡散/浸透しないた
め、実用的な時間で塗装樹脂、プライマー樹脂の剥離が
起こらない。一方、温度 150度より高い場合では、樹脂
部品本体の溶融および熱劣化、酸化劣化を引き起こして
しまう。本発明の樹脂塗膜の剥離除去方法において、前
記剥離除去剤による処理方法は、工業的観点から、前記
剥離除去剤に上記樹脂部品を浸漬するか、あるいは前記
剥離除去剤の蒸気に、上記樹脂部品をさらすことにより
実施可能である。
Next, the use temperature of the stripping and removing agent for the resin coating film is 50 to 150 ° C, preferably 60 to 100 ° C. Five
At a use temperature lower than 0 ° C., the peeling / removing agent does not diffuse / permeate into the coating resin and the primer resin sufficiently quickly, so that the coating resin and the primer resin do not peel in a practical time. On the other hand, if the temperature is higher than 150 ° C, melting, heat deterioration and oxidative deterioration of the resin component body will occur. In the method for peeling and removing the resin coating film of the present invention, the treatment method using the peeling and removing agent is, from an industrial viewpoint, immersing the resin component in the peeling and removing agent, or in the vapor of the peeling and removing agent, the resin. This can be done by exposing the parts.

【0015】[0015]

【実施例】以下本発明を実施例および比較例により説明
する。樹脂塗膜の剥離除去剤の調製例 室温で前記化合物A(液体)およびB(液体)を各々の
ビーカーに注ぎ、自動天秤にて所定重量秤量し、二液を
混合後、マグネチックスターラー、攪拌子を用いて攪拌
して、樹脂塗膜の剥離除去剤を調製した。
EXAMPLES The present invention will be described below with reference to examples and comparative examples. Preparation Example of Peeling Remover for Resin Coatings At room temperature, the above compounds A (liquid) and B (liquid) were poured into respective beakers and weighed with an automatic balance to a predetermined weight. After mixing the two liquids, a magnetic stirrer and stirring were performed. A peeling remover for the resin coating film was prepared by stirring with a child.

【0016】表1、表2の塗膜剥離除去評価結果に具体
的な塗膜剥離除去剤の調製例を示した。尚、工業的に
は、前記化合物A、Bの密度を利用し、重量換算した体
積を秤量して前記樹脂塗装分解除去剤を調製することも
可能である。
The results of the coating film peeling removal evaluations in Tables 1 and 2 show specific preparation examples of the coating film peeling remover. Incidentally, industrially, it is possible to prepare the resin coating decomposition remover by utilizing the densities of the compounds A and B and weighing the volume in terms of weight.

【0017】樹脂塗膜分解除去評価試験例 次に、前記樹脂塗膜の剥離除去剤を適量(約100ml)ナス
型フラスコに取りマグネチックスターラー攪拌子にて、
設定温度(50/150 ℃)になるまで、還流した。前記剥離
除去剤を設定温度に保持した後、樹脂塗装処理樹脂部品
から、切り出した横約10mm×縦約10mm×厚約2mmの割断
片5個を、フラスコ内に投入し、前記分解除去剤に浸漬
し、30分間放置、観察した。その後、フラスコより割断
片を取りだし、目視にて、樹脂塗装分解除去状態を判定
した。
Test Example for Degradation and Removal of Resin Coating Film Next, an appropriate amount (about 100 ml) of the above-described resin coating peeling and removing agent was placed in a round-bottomed flask with a magnetic stirrer stirrer.
Reflux was carried out until the temperature reached the set temperature (50/150 ° C). After holding the peeling remover at the set temperature, 5 pieces of the cut pieces of about 10 mm in width × about 10 mm in length × about 2 mm in thickness cut out from the resin part treated with the resin coating are put into the flask to be the decomposition removing agent. It was immersed, left for 30 minutes and observed. Then, the split pieces were taken out from the flask, and the state of decomposition and removal of the resin coating was visually determined.

【0018】表1、表2の塗装剥離除去評価において、
具体的な評価試験例を示した。尚、評価試験に供した樹
脂塗装処理樹脂の種類は、2種(I,II)で両者は、
塗装樹脂、プライマー樹脂の化学組成が異なる。表1、
表2中、評価試験後、塗装樹脂、プライマー樹脂に変化
が観察された場合、プライマー樹脂が分解または膨潤剥
離された場合は◎印、塗装樹脂が分解または膨潤剥離さ
れた場合は○印、一部溶解または分解または膨潤剥離が
認められた場合はΔ印、変化が認められない場合は×印
の覧にそれぞれ変化した個数を示した(試験試料はそれ
ぞれ5個とした)。
In the coating peeling removal evaluation of Table 1 and Table 2,
A specific evaluation test example was shown. The types of resin coating resin used in the evaluation test are two types (I, II).
The coating resin and primer resin have different chemical compositions. Table 1,
In Table 2, after the evaluation test, when a change was observed in the coating resin and the primer resin, when the primer resin was decomposed or swelled and peeled off, ∘, and when the coating resin was decomposed or swelled and peeled, ◯, one When partial dissolution or decomposition or swelling and peeling were observed, Δ mark was shown, and when no change was observed, the number of changed was shown in the mark of X mark (5 test samples were used respectively).

【0019】実施例1 樹脂塗膜の剥離除去剤(N,N−ジメチルホルムアミド
/エタノール=10重量%/90重量%)の約100ml を200m
l のナス型フラスコに取り、ウォーターバス上、マグネ
チックスターラーを用いて攪拌し、所定温度(50 ℃、80
℃又は100 ℃)になるまで還流した。次に、樹脂塗装部
品(塗装品I,II)の割断片(横×縦×厚=10×10×
2mm) を各5個切り出し、フラスコ中の樹脂塗膜剥離除
去剤液中へ浸漬し、30分間処理した。その後、フラスコ
の内容物をビーカーに取り出し、割断片の樹脂塗装、プ
ライマー樹脂の分解程度を目視にて確認した。得た結果
は表1に示す通りである。実施例2〜31、比較例1〜14 表1に示す実施例2〜31、表2に示す比較例1〜14の各
樹脂塗膜の剥離除去剤を使用し、所定温度を表1に示す
温度(ウォーターバス又は、オイルバス加温)とした以
外は、実施例1と同様にして樹脂塗装部品の割断片を処
理し、各割断片の塗装樹脂、プライマー樹脂の剥離状態
を目視にて確認した。得た結果は表1、表2に示す通り
である。
Example 1 About 100 ml of a stripping and removing agent for resin coating (N, N-dimethylformamide / ethanol = 10% by weight / 90% by weight) was added to 200 m.
Transfer to a l-shaped eggplant-shaped flask, stir on a water bath using a magnetic stirrer, and stir at the specified temperature (50 ℃, 80
The mixture was refluxed until the temperature reached ℃ or 100 ℃. Next, split pieces (horizontal x vertical x thickness = 10 x 10 x) of resin coated parts (painted items I and II)
Five pieces each of 2 mm) were cut out, immersed in the resin coating film peeling remover liquid in the flask, and treated for 30 minutes. Then, the contents of the flask were taken out into a beaker, and the resin coating of the split pieces and the degree of decomposition of the primer resin were visually confirmed. The obtained results are as shown in Table 1. Examples 2 to 31, Comparative Examples 1 to 14 The peeling and removing agents for the resin coatings of Examples 2 to 31 shown in Table 1 and Comparative Examples 1 to 14 shown in Table 2 are used, and the predetermined temperatures are shown in Table 1. Except for the temperature (water bath or oil bath heating), the split pieces of the resin-coated parts were treated in the same manner as in Example 1, and the peeling state of the coating resin and primer resin of each split piece was visually confirmed. did. The obtained results are as shown in Tables 1 and 2.

【0020】[0020]

【表1】 [Table 1]

【0021】[0021]

【表2】 [Table 2]

【0022】[0022]

【発明の効果】以上説明してきたように、本発明の樹脂
剥離分解除去剤は10〜90重量%の濃度を有する化合物A
と10〜90重量%の化合物Bとから構成したことにより、
50乃至150 ℃の温度で、該剥離除去剤を樹脂塗装処理樹
脂部品に噴霧若しくは塗布するか、或いは該分解除去剤
に浸漬/塗布するか、或いは除去剤の蒸気にさらすこと
により環境衛生を悪化させることも、オゾン層破壊を引
き起こすこともなく好首尾にまた、効率的に樹脂塗膜を
分解除去することができるという効果が得られる。ま
た、プライマー面も同時に除去されることからこれらの
材料を用いて混練り等を行った場合、加工機器の接触表
面の腐食等も防止される。
As described above, the resin peeling decomposition removing agent of the present invention has the compound A having a concentration of 10 to 90% by weight.
And 10 to 90% by weight of Compound B,
Deterioration of environmental hygiene by spraying or applying the exfoliation remover to resin coating treated resin parts, dipping / applying to the decomposition remover, or exposing to the vapor of the remover at a temperature of 50 to 150 ° C. By doing so, it is possible to obtain an effect that the resin coating film can be decomposed and removed efficiently and successfully without causing ozone layer destruction. Further, since the primer surface is also removed at the same time, when kneading or the like using these materials, the corrosion of the contact surface of the processing equipment is prevented.

【図面の簡単な説明】[Brief description of drawings]

【図1】樹脂塗装処理樹脂部品の断面図である。FIG. 1 is a cross-sectional view of a resin-coated resin component.

【図2】(a) 樹脂塗装処理樹脂部品の塗膜を本発明の一
例の樹脂塗膜の剥離除去剤によって剥離した状態を示す
説明図であり、(b) 樹脂塗装処理樹脂部品の塗膜を本発
明の他の例の樹脂塗膜の剥離除去剤によって剥離した状
態を示す説明図であり、(c) 樹脂塗装処理樹脂部品の塗
膜を本発明の他の例の樹脂塗膜の剥離除去剤によって剥
離した状態を示す説明図である。
FIG. 2 (a) is an explanatory view showing a state in which a coating film of a resin coating treated resin part is peeled off by a peeling remover for a resin coating film of an example of the present invention, and (b) a coating film of a resin coating treated resin part. It is an explanatory view showing a state of peeling by a peeling remover of the resin coating film of another example of the present invention, (c) peeling of the coating film of the resin coating treated resin component of the resin coating film of another example of the present invention It is explanatory drawing which shows the state peeled by the remover.

【符号の説明】[Explanation of symbols]

1 塗装樹脂層 2 プライマー樹脂層 3 樹脂基材 4 塗膜剥離部 1 Coating resin layer 2 Primer resin layer 3 resin base material 4 Coating film peeling part

Claims (3)

【特許請求の範囲】[Claims] 【請求項1】 非プロトン性溶媒、或いはイミン類また
はケトン類などの異種原子間に不飽和結合を有する化合
物Aを10〜90重量%、および沸点が250 ℃以下の常温で
液体状態を呈する、一価以上のアルコール類或いはその
誘導体から成る化合物Bを10〜90重量%含有することを
特徴とする樹脂塗膜の剥離除去剤。
1. An aprotic solvent, or 10 to 90% by weight of a compound A having an unsaturated bond between different atoms such as imines or ketones, and a liquid state at room temperature having a boiling point of 250 ° C. or lower, A peeling remover for a resin coating film, which comprises 10 to 90% by weight of a compound B consisting of a monohydric or higher alcohol or its derivative.
【請求項2】 50〜150 ℃の温度でアクリル系或いはメ
ラミン系或いはウレタン系樹脂塗料に対して、化合物A
及び化合物Bの混合溶液から成る樹脂塗膜の剥離除去剤
で膨潤させた場合、膨潤率(ΔWs)20%以上になるこ
とを特徴とする請求項1の樹脂塗膜の剥離除去剤。
2. A compound A for acrylic, melamine or urethane resin coating at a temperature of 50 to 150.degree.
The swelling ratio (ΔWs) is 20% or more when swollen with a resin film stripping and removing agent consisting of a mixed solution of the compound B and the compound B.
【請求項3】 50〜150 ℃で請求項1記載の樹脂塗膜の
剥離除去剤を樹脂塗装部品に噴霧若しくは塗布するか、
或いは前記樹脂塗膜の剥離除去剤に樹脂塗装部品を浸漬
することを特徴とする樹脂塗膜の剥離除去方法。
3. A method for peeling and removing the resin coating film according to claim 1 at 50 to 150.degree.
Alternatively, a method for peeling and removing a resin coating film, which comprises immersing a resin coated part in the above-mentioned resin film peeling and removing agent.
JP3185834A 1991-03-25 1991-07-01 Removal agent and method for removing resin film Expired - Fee Related JP2924323B2 (en)

Priority Applications (4)

Application Number Priority Date Filing Date Title
JP3185834A JP2924323B2 (en) 1991-07-01 1991-07-01 Removal agent and method for removing resin film
US07/856,794 US5256210A (en) 1991-03-25 1992-03-24 Stripping composition for resin paint material and a method of removing resin paint materials
GB9226893A GB2273715B (en) 1991-03-25 1992-12-23 A stripping composition for resin paint material and a method of removing resin paint materials
DE4244355A DE4244355C2 (en) 1991-03-25 1992-12-28 Resin paint material stripping composition and resin paint material removal method

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
JP3185834A JP2924323B2 (en) 1991-07-01 1991-07-01 Removal agent and method for removing resin film
GB9226893A GB2273715B (en) 1991-03-25 1992-12-23 A stripping composition for resin paint material and a method of removing resin paint materials
DE4244355A DE4244355C2 (en) 1991-03-25 1992-12-28 Resin paint material stripping composition and resin paint material removal method

Publications (2)

Publication Number Publication Date
JPH059419A true JPH059419A (en) 1993-01-19
JP2924323B2 JP2924323B2 (en) 1999-07-26

Family

ID=27204618

Family Applications (1)

Application Number Title Priority Date Filing Date
JP3185834A Expired - Fee Related JP2924323B2 (en) 1991-03-25 1991-07-01 Removal agent and method for removing resin film

Country Status (1)

Country Link
JP (1) JP2924323B2 (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH0593157A (en) * 1991-07-01 1993-04-16 Nissan Motor Co Ltd Method of stripping resin coating and method of post-treatment
JP2015217332A (en) * 2014-05-15 2015-12-07 Jfeエンジニアリング株式会社 Peeling method of coating film and coating film peeling agent

Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS4945945A (en) * 1972-09-07 1974-05-02
JPS63163457A (en) * 1986-12-26 1988-07-06 Asahi Chem Ind Co Ltd Peeling composition for photoresist
JPH04293974A (en) * 1991-03-25 1992-10-19 Nissan Motor Co Ltd Liquid releasing composition for separating coating resin film and method for separation
JPH04293975A (en) * 1991-03-25 1992-10-19 Nissan Motor Co Ltd Liquid composition for removing coating resin film and method for removal
JPH0593157A (en) * 1991-07-01 1993-04-16 Nissan Motor Co Ltd Method of stripping resin coating and method of post-treatment

Patent Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS4945945A (en) * 1972-09-07 1974-05-02
JPS63163457A (en) * 1986-12-26 1988-07-06 Asahi Chem Ind Co Ltd Peeling composition for photoresist
JPH04293974A (en) * 1991-03-25 1992-10-19 Nissan Motor Co Ltd Liquid releasing composition for separating coating resin film and method for separation
JPH04293975A (en) * 1991-03-25 1992-10-19 Nissan Motor Co Ltd Liquid composition for removing coating resin film and method for removal
JPH0593157A (en) * 1991-07-01 1993-04-16 Nissan Motor Co Ltd Method of stripping resin coating and method of post-treatment

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH0593157A (en) * 1991-07-01 1993-04-16 Nissan Motor Co Ltd Method of stripping resin coating and method of post-treatment
JP2015217332A (en) * 2014-05-15 2015-12-07 Jfeエンジニアリング株式会社 Peeling method of coating film and coating film peeling agent

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