JP2924323B2 - Removal agent and method for removing resin film - Google Patents
Removal agent and method for removing resin filmInfo
- Publication number
- JP2924323B2 JP2924323B2 JP3185834A JP18583491A JP2924323B2 JP 2924323 B2 JP2924323 B2 JP 2924323B2 JP 3185834 A JP3185834 A JP 3185834A JP 18583491 A JP18583491 A JP 18583491A JP 2924323 B2 JP2924323 B2 JP 2924323B2
- Authority
- JP
- Japan
- Prior art keywords
- resin
- coating
- stripping
- removing agent
- compound
- 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 - Fee Related
Links
Landscapes
- Paints Or Removers (AREA)
Description
【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。BACKGROUND OF THE INVENTION Paint removal agent and paint removal for resin parts with effective paint removal performance, good workability, and high environmental safety in the resin coating processing process or the pretreatment process for recycled materials. Law is required. The present invention relates to a stripping / removing agent for a resin coating which does not cause destruction of the ozone layer and is excellent in handleability, and a method for stripping / removing a resin coating using the stripping / 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 Conventional stripping agents for resin coatings include chloropentafluoropropane / 1,1-dichloro-1-trifluoroethane mixed solvent composition (JP-A-2-286795) and chloropentafluoropropane / solvent. A dichlorotrifluoroethane mixed solvent composition (JP-A-2-286796) and the like have been proposed. In addition, the inventors have already prepared a resin coating stripping / removing agent composition solution and a removing method (Japanese Patent Application No. 3-8300).
No. 9) presented a solvent or solution composition capable of physically or chemically stripping the coating. Further, ordinary halogen solvents such as methylene chloride, strong alkaline solutions or strong acid solutions are 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。SUMMARY OF THE INVENTION The above-mentioned Japanese Patent Application Laid-Open No. 2-286795.
The mixed solvent compositions disclosed in Japanese Patent Application Laid-Open Nos. 2-286796 and 2002-286796 are excellent in detergency against oils and fats and have a low risk of destruction of the ozone layer. And the use of a large number of halogen atoms (F, C1) in the molecular chain, there is a problem that attention must be paid to handling in terms of environmental hygiene. In addition, there is a problem that the use of a normal halogen-based solvent deteriorates environmental hygiene and also causes ozone layer destruction. Even in the use of a strong alkaline solution or a strong acid solution, there are problems such as work safety and environmental safety, as well as complication that a post-treatment step such as neutralization is essential. Further, in the mixed solvent composition described in the specification of Japanese Patent Application No. 3-83009, the peeling of the primer surface made of chlorinated polyolefin or the like was insufficient depending on the composition of the coating resin.
When kneading or the like is performed using a material with insufficient primer surface peeling, there is a problem that corrosion occurs 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、1,3−ジメチル−2−イミダゾ
リジノンを10〜90重量%、好ましくは20〜80重量%およ
び沸点が250 ℃以下の常温で液体状態を呈する、モノオ
ール類、ジオール類又はチオール類から成る化合物Bを
10〜90重量%、好ましくは20〜80重量%含有することを
特徴とするプライマー樹脂層と塗装樹脂層を有する樹脂
塗装処理部品の樹脂塗膜の剥離除去剤を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 in view of such a conventional problem, and 10-90% by weight, preferably 20-80% by weight of 1,3-dimethyl-2-imidazolidinone and a boiling point of 1,3-dimethyl-2-imidazolidinone. Compound B consisting of monools, diols or thiols, which is in a liquid state at a normal temperature of 250 ° C. or less,
10 to 90% by weight, preferably 20 to 80% by weight of a resin coating component having a primer resin layer and a coating resin layer.
Preferably, the above-mentioned problems are solved by applying the resin component to a resin-coated resin part at a temperature of 50 to 100 ° C. or by immersing the resin part in the peeling-off.
【0005】本発明のプライマー樹脂層と塗装樹脂層を
有する樹脂塗装処理部品の樹脂塗膜の樹脂塗膜剥離除去
剤は、1,3−ジメチル−2−イミダゾリジノン化合物
Aを10〜90重量%、好ましくは20〜80重量%および沸点
が250 ℃以下の常温で液体状態を呈する、モノオール
類、ジオール類又はチオール類から成る化合物Bを10〜
90重量%、好ましくは20〜80重量%含有することを特徴
とする。[0005] The resin coating film peeling and removing agent of the resin coating film of the resin-coated part having the primer resin layer and the coating resin layer of the present invention is 1,3-dimethyl-2-imidazolidinone compound A in an amount of 10 to 90% by weight. %, Preferably 20 to 80% by weight and a compound B consisting of a monool, diol or thiol, which is in a liquid state at room temperature having a boiling point of 250 ° C. or less.
It is characterized by containing 90% by weight, preferably 20-80% by weight.
【0006】[0006]
【0007】本発明の樹脂塗膜の剥離除去剤を構成する
化合物Aとしては、非プロトン性溶剤である1,3−ジ
メチル−2−イミダゾリジノンが用いられる。As the compound A constituting the stripping / removing agent of the resin coating film of the present invention, 1,3-dimethyl-2-imidazolidinone which is an aprotic solvent is 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。The compound B includes 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 represents C n H 2 n + 1 (n = 1 to 10) or an aromatic group].
【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 compound A mainly diffuses / permeates into the primer resin, swells and swells the primer resin, and peels it off. Therefore, when the concentration of Compound A is less than 10% by weight, the primer resin does not sufficiently swell and expand,
The paint does not peel. On the other hand, when the amount of the compound A is more than 90% by weight, the swelling of the coating resin is insufficient and the coating may not be peeled off. When the resin-coated resin component swells with respect to the above-mentioned coating film peeling remover, and when the mass change rate is less than 20%, the swelling of the coating resin is insufficient and the coating resin cannot be peeled. On the other hand, the above-mentioned compound B having a mono-, diol or derivative thereof is used as the release remover for the resin coating film.
Is contained in an amount of 10 to 90% by weight, preferably 20 to 80% by weight. Compound B mainly diffuses / permeates the coating resin, swells and swells the coating resin, and promotes diffusion / permeation of compound A. Further, since compound B has a hydrophilic and lipophilic group, it also has an effect on the penetration of the coating film peeling remover from the interface of the coating resin / primer resin / resin part.
【0010】しかし、炭素連鎖長が10以上の化合物B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 B having a carbon chain length of 10 or more is used, the boiling point exceeds 250 ° C., the viscosity of the solution increases, the lipophilicity increases, the solubility in water decreases significantly, and the resin is removed and removed. Since the film wettability and diffusion / penetration by the agent and the workability such as the drying step are impaired, n-
Dodecyl alcohol is not suitable for use. On the other hand, 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 stripping / removing agent for resin coatings of the present invention is particularly preferably used for stripping / removing resin coatings from acrylic-, melamine- or urethane-based resin paint-treated resin parts. The peeling removal can be carried out by spraying or applying the peeling remover to the resin paint part as described above, or by immersing the resin paint part in the peel 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 diagram showing a cross section of a resin-coated part. From the painted surface side,
It comprises a coating resin layer 1, a primer resin layer 2, and a lowermost resin base material 3. Using the resin film peeling remover and the peeling removal method of the present invention, from the resin coated parts,
Fig. 2 (a) shows three types of peeling mechanisms for removing and removing paint.
(b) and (c). FIG. 2A shows that the coating resin layer 1 swells and expands significantly as compared to the primer resin layer 2 mainly due to the action of the compound B, and peels off near the interface 4 between the coating resin layer 1 and the primer resin layer 2. Conversely, in FIG. 2 (b), the primer resin 2 swells and expands significantly compared to the coating resin layer 1 mainly due to the action of the compound A, and the coating resin layer 1 / primer resin layer 2 or the primer resin layer 2 / resin This indicates that the separation occurs near the interface 4 of the substrate 3. Next, in FIG. 2 (c), the coating resin layer 1 and the primer resin layer 2 swell and swell due to the action of both the compounds A and B, but the swelling of the primer layer 2 having a low degree of curing remarkably progresses, and 2 / It is shown that peeling occurs near the interface 4 of the resin substrate 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. In addition, paint peeling is observed. In addition, in the above-mentioned coating peeling, no swelling or swelling of the resin base material 3 is observed. The degree of swelling (ΔWs) is defined as follows. ΔWs (%) = 100 (Ws−Wo) / Wo Wo: Swelling with paint film removing agent, coating resin layer 1 before swelling
Alternatively, the weight of the primer resin layer 2 Ws: after swelling and swelling with the coating film peeling and removing agent (temperature: 50 to 1
Weight of coating resin layer 1 or primer resin layer 2 (50 ° C, treatment 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 / removing agent for the resin film is 50 to 150 ° C., preferably 60 to 100 ° C. Five
At a use temperature lower than 0 ° C., the peeling-off remover does not diffuse / permeate into the coating resin and the primer resin sufficiently quickly, so that the peeling of the coating resin and the primer resin does not occur in a practical time. On the other hand, if the temperature is higher than 150 degrees, the resin component body will be melted, thermally degraded and oxidized. In the method for stripping and removing a resin coating film of the present invention, the treatment method using the stripping and removing agent may be, from an industrial viewpoint, immersing the resin component in the stripping or removing agent or vaporizing the stripping and removing agent with 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。The present invention will be described below with reference to examples and comparative examples. Preparation example of resin film peeling and removing agent The compounds A (liquid) and B (liquid) were poured into each beaker at room temperature, weighed by an automatic balance to a predetermined weight, and the two liquids were mixed. The mixture was agitated with a sliver to prepare a peeling remover for the resin coating film.
【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。Tables 1 and 2 show the results of the evaluation of the removal of the coating film, and specific preparation examples of the coating film removing agent are shown. In addition, industrially, it is also possible to prepare the resin coating decomposition removal agent by weighing the volume in terms of weight using the density of the compounds A and B.
【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。[0017] In the resin coating film decomposed and removed Evaluation Test Examples proper amount of peel removal agent of the resin film (about 100ml) placed in a round-bottom flask magnetic stirrer stirring element,
The mixture was refluxed until the set temperature (50/150 ° C.) was reached. After keeping the peeling remover at a set temperature, five pieces of about 10 mm wide × about 10 mm long × about 2 mm thick cut out from the resin-coated resin part are put into a flask, and the decomposition remover It was immersed, left for 30 minutes, and observed. Thereafter, the split pieces were taken out of 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 evaluation of removal of paint peeling in Tables 1 and 2,
Specific evaluation test examples are shown. In addition, the kind of resin coating treatment resin used for the evaluation test was two kinds (I, II), and both were:
The chemical compositions of the coating resin and primer resin are different. Table 1,
In Table 2, when a change was observed in the coating resin and the primer resin after the evaluation test, a mark ◎ indicates that the primer resin was decomposed or swelled and peeled, and a mark ○ indicates that the coating resin was decomposed or swelled and peeled. When partial dissolution, decomposition, or swelling and peeling were observed, the number of changes was shown in the list of Δ marks, and in the case of no change, the number of changed pieces was shown in the list (5 test samples each).
【0019】実施例1 樹脂塗膜の剥離除去剤(1,3−ジメチル−2−イミダ
ゾリジノン/エタノール=10重量%/90重量%)の約10
0ml を200ml 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2〜5、比較例1〜14 表1に示す実施例2〜5、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 10% of a stripping and removing agent (1,3-dimethyl-2-imidazolidinone / ethanol = 10% by weight / 90% by weight) of a resin coating film
Take 0 ml into a 200 ml eggplant-shaped flask, stir on a water bath with a magnetic stirrer,
(50 ° C., 80 ° C. or 100 ° C.). next,
Cut out 5 pieces (width × length × thickness = 10 × 10 × 2 mm) of each of the resin-coated parts (painted products I and II), immerse them in the resin film peeling / removal agent in the flask, and treat for 30 minutes did. Thereafter, 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 checked. The results obtained are as shown in Table 1. Examples 2 to 5 and Comparative Examples 1 to 14 Table 1 shows the predetermined temperatures using the stripping and removing agents for the resin coatings of Examples 2 to 5 shown in Table 1 and Comparative Examples 1 to 14 shown in Table 2. Except that the temperature (water bath or oil bath heating) was used, the split pieces of the resin-coated part 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 checked. 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 stripping / decomposing / removing agent of the present invention has a concentration of 10 to 90% by weight of compound A.
And 10 to 90% by weight of Compound B,
At a temperature of 50 to 150 ° C., the delamination-removing agent is sprayed or applied to the resin-coated resin parts, or is immersed / applied to the decomposition-removing agent, or is exposed to the vapor of the removing agent, thereby deteriorating environmental health. Also, the effect that the resin coating film can be efficiently decomposed and removed without causing ozone layer destruction can be obtained successfully. In addition, since the primer surface is also removed at the same time, when kneading or the like is performed using these materials, corrosion of the contact surface of the processing equipment is prevented.
【図面の簡単な説明】[Brief description of the drawings]
【図1】樹脂塗装処理樹脂部品の断面図である。FIG. 1 is a sectional view of a resin part subjected to a resin coating treatment.
【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 the coating film of the resin coating-treated resin part is peeled off by the peeling and removing agent of the resin coating film of one example of the present invention, and (b) the coating film of the resin coating-treated resin part. It is an explanatory view showing a state in which the resin coating film of another example of the present invention is peeled off by a resin film peeling and removing agent of another example of the present invention, It is explanatory drawing which shows the state peeled by the removing agent.
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 Reference Signs List 1 coating resin layer 2 primer resin layer 3 resin substrate 4 coating film peeling part
フロントページの続き (56)参考文献 特開 昭63−163457(JP,A) 特開 昭49−45945(JP,A) 特開 平4−293974(JP,A) 特開 平4−293975(JP,A) 特開 平5−93157(JP,A) 特公 昭45−12925(JP,B1) (58)調査した分野(Int.Cl.6,DB名) C09D 9/00 - 9/04 Continuation of the front page (56) References JP-A-63-163457 (JP, A) JP-A-49-45945 (JP, A) JP-A-4-293974 (JP, A) JP-A-4-293975 (JP) , A) JP-A-5-93157 (JP, A) JP-B-45-12925 (JP, B1) (58) Fields investigated (Int. Cl. 6 , DB name) C09D 9/00-9/04
Claims (3)
ン化合物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、モノオール類、ジオール類又
はチオール類から成る化合物Bを10〜90重量%含有する
ことを特徴とするプライマー樹脂層と塗装樹脂層を有す
る樹脂塗装処理部品の樹脂塗膜の剥離除去剤。1. A monool, diol or thiol, which is in a liquid state at 10 to 90% by weight of 1,3-dimethyl-2-imidazolidinone compound A and a boiling point of 250 ° C. or less at room temperature. A stripping / removing agent for a resin coating of a resin-coated part having a primer resin layer and a coating resin layer, comprising 10 to 90% by weight of Compound B.
ラミン系或いはウレタン系樹脂塗料に対して、請求項1
記載の化合物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. An acrylic, melamine or urethane resin paint at a temperature of 50 to 150 ° C.
When swelled with a stripping and removing agent for a resin coating consisting of a mixed solution of the described compound A and compound B, the swelling ratio (ΔWs)
% Or more.
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. The method according to claim 1, wherein the resin coating stripping and removing agent is sprayed or applied to the resin-coated part at 50 to 150 ° C.
Alternatively, a method for stripping and removing a resin coating film, comprising immersing a resin-coated component in the stripping and removing agent for the resin coating film.
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 JPH059419A (en) | 1993-01-19 |
| JP2924323B2 true 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) |
Families Citing this family (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH0593157A (en) * | 1991-07-01 | 1993-04-16 | Nissan Motor Co Ltd | Resin coating peeling removal method and post-treatment method |
| JP2015217332A (en) * | 2014-05-15 | 2015-12-07 | Jfeエンジニアリング株式会社 | Coating film peeling method and coating film peeling agent |
Family Cites Families (5)
| 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 |
| JP2910292B2 (en) * | 1991-03-25 | 1999-06-23 | 日産自動車株式会社 | Resin coating remover composition liquid and removal method |
| JP2861451B2 (en) * | 1991-03-25 | 1999-02-24 | 日産自動車株式会社 | Resin coating release agent composition liquid and release method |
| JPH0593157A (en) * | 1991-07-01 | 1993-04-16 | Nissan Motor Co Ltd | Resin coating peeling removal method and post-treatment method |
-
1991
- 1991-07-01 JP JP3185834A patent/JP2924323B2/en not_active Expired - Fee Related
Also Published As
| Publication number | Publication date |
|---|---|
| JPH059419A (en) | 1993-01-19 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| DE69433895T2 (en) | An aqueous stripping composition containing hydroxylamine and an alkanolamine and their use. | |
| EP1016699B1 (en) | Use of a solvent composition comprising an oxyisobutyric acid ester as a cleaning agent | |
| US4640719A (en) | Method for printed circuit board and/or printed wiring board cleaning | |
| JP2924323B2 (en) | Removal agent and method for removing resin film | |
| JPH03505349A (en) | Compositions for stripping tin or tin-lead alloys from copper surfaces, including alkanesulfonic acid and ferric nitrate, and methods for stripping tin or tin-lead alloys | |
| US5053256A (en) | Sodium hypochlorite surface treatment to improve the adhesion of paints to polydicyclopentadiene | |
| CH617229A5 (en) | ||
| JP2910337B2 (en) | Decomposition / removal agent for resin coating and method for decomposition / removal of resin coating | |
| KR0156084B1 (en) | Remover composition for photoresist removal and method for removing photoresist using same | |
| JP2861451B2 (en) | Resin coating release agent composition liquid and release method | |
| JP2003282518A (en) | Organic film removal method and remover | |
| US20030192572A1 (en) | Method of removing organic materials using aqueous cleaning solutions | |
| JPH1121482A (en) | Coating release agent composition | |
| CN115261860B (en) | Aluminum alloy surface corrosion scavenger and preparation method and application thereof | |
| JPS6084373A (en) | Stripping agent composition | |
| DE4244355C2 (en) | Resin paint material stripping composition and resin paint material removal method | |
| JPH0593157A (en) | Resin coating peeling removal method and post-treatment method | |
| US5165962A (en) | Masking film composition and method of masking an article using same | |
| JPH10292138A (en) | Composition for peeling coating film | |
| FR2801893A1 (en) | COMPOSITION FOR COATING BY CHEMICAL GRAFTING, METHOD FOR USING SAME AND PRODUCT OBTAINED | |
| EP0688860A1 (en) | Process for producing clean article | |
| JPH0427298B2 (en) | ||
| CN1103964A (en) | Glue removing composition agent | |
| JP2910292B2 (en) | Resin coating remover composition liquid and removal method | |
| JPH06336598A (en) | Cleaning composition |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| LAPS | Cancellation because of no payment of annual fees |