JPH0588262B2 - - Google Patents
Info
- Publication number
- JPH0588262B2 JPH0588262B2 JP60090534A JP9053485A JPH0588262B2 JP H0588262 B2 JPH0588262 B2 JP H0588262B2 JP 60090534 A JP60090534 A JP 60090534A JP 9053485 A JP9053485 A JP 9053485A JP H0588262 B2 JPH0588262 B2 JP H0588262B2
- Authority
- JP
- Japan
- Prior art keywords
- resin product
- treatment
- plasma
- bumper
- polyolefin resin
- 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 - Lifetime
Links
Landscapes
- Application Of Or Painting With Fluid Materials (AREA)
- Treatments Of Macromolecular Shaped Articles (AREA)
Description
(産業上の利用分野)
本発明はポリエチレン(PE)或いはポリプ
ロピレン(PP)等のポリオレフイン系樹脂製
品の塗装前処理方法に関する。
(従来の技術)
ポリエチレン或いはポリプロピレン等は樹脂
自体に着色を施すことが可能であるため、一般
的には塗装する必要はない。しかしながら、例
えば自動車用バンパーを上記樹脂を成形するこ
とで得るようにした場合、自動車用バンパーの
一部を他の部分との関係で塗布したり、色分け
塗装を施すことが必要となる場合がある。
一方、オレフイン系樹脂は表面エネルギーが
低く塗膜接着力が極めて弱い。そこで、従来か
ら、トリクロルエチレン等の塩素系有機溶剤に
よつて樹脂製品の表面を処理した後、プライマ
ーを塗装したり、或いは特開昭57−15870号に
開示されるように、トリクロルエチレンによつ
て表面処理した後、酸化性低温プラズマ処理を
行う塗装前処理方法が提案されている。
(発明が解決しようとする問題点)
上述した方法、つまりトリクロルエチレン等
の塩素系有機溶剤によつてポリオレフイン系樹
脂表面を処理する方法にあつては、トリクロル
エチレン等は毒性が強く、洗浄用水の排水及び
操業上の管理に細心の注意を払わなければなら
ず、更にトリクロルエチレン等の有機溶剤にて
表面処理を施した場合には樹脂製品表面が粗面
化され過ぎ、プラズマ処理を施す場合には所謂
オーバーエツチングを呈し、却つて塗膜の剥離
強度が低下する不都合がある。
(問題点を解決するための手段)
上記問題点を解決すべく本発明は、トリクロ
ルエチレン等の塩素系有機溶剤の代りに、水溶
性の無機溶剤からなる脱脂剤を用いて、ポリオ
レフイン系樹脂製品の表面を脱脂した後、O2
プラズマによつて該表面を処理し、樹脂製品表
面の塗膜接着力を高めるようにした。
(作用)
ポリオレフイン系樹脂製品の表面を水溶性の
無機溶剤からなる脱脂剤で処理することによ
り、樹脂製品表面の油類の除去が簡単に行わ
れ、又、有機溶剤で処理するような不具合、す
なわち極端な粗面化によるオーバーエツチング
の状態を避けることが出来る。
又、排水処理も洗浄用水を中和するだけで済
むために処理容易であり、しかも、例えば有機
溶剤のような蒸発に起因する大気汚染、引火等
の危険性もなく操業上の管理も容易である。
又、蒸発に伴う不足分を再供給する必要もな
く、いわゆるランニングコストが安価である。
(実施例)
以下に本発明の実施例を添付図面を参照しつ
つ説明する。尚、実施例にあつてはポリオレフ
イン系樹脂製品として自動車用バンパーを示し
た。
先ず本発明にあつては第1図に示す如く、成
形後の自動車用バンパー1を脱脂槽2内に浸漬
してバンパー1表面の脱脂を行う。ここでバン
パー1を構成するポリオレフイン系樹脂として
は、例えばポリエチレン、ポリプロピレン、ポ
リエチレンホモポリマ、ポリプロピレンホモポ
リマ、エチレン酢酸ビニルコポリマ、エチレン
アクリレートコポリマ、エチレンプロピレンコ
ポリマ及びこれらの単体もしくはこれらの混合
物に熱可塑性エラストマー、無機フイラー、ガ
ラス繊維等を混入させたものが挙げられる。
また、脱脂剤としては水溶性の無機溶剤から
なる脱脂剤、具体的にはメタケイ酸ソーダ等を
用いる。尚、実施例にあつては、ハンガー3に
よつてバンパー1を吊下げ支持した状態で脱脂
槽2内に浸漬するようにしたが、スプレーガン
等によつてバンパー1表面に脱脂剤を吹付ける
ようにしてもよい。
このようにして、バンパー1表面の脱脂処理
が終了したならば、第2図に示す如く、バンパ
ー1を台4に載置したままプラズマ処理装置5
内に搬入し、バンパー1表面をO2プラズマで
処理する。すると、ポリオレフイン系樹脂の如
く酸素を含まない高分子は活性な酸素ラジカル
をカルボニル結合として高分子中に多量に取込
み、表面エネルギーが高まり、塗膜の接着力が
大巾に高まる。
ここでプラズマ処理の条件としては、プラズ
マ処理槽、処理される製品形状等により異なる
が、酸素ガスを処理ガスとして用いる場合に
は、真空度を0.3〜5.0Torr、周波数を2450±
10MHz、処理時間を5〜300秒とするのが好ま
しい。
而る後、第3図に示す如くスプレーガン6に
てウレタン系二液型の塗料7を上塗りして製品
を得る。
次に具体的な実験結果を「表」に示し、従来
例と比較する。
(Field of Industrial Application) The present invention relates to a method for pre-painting a polyolefin resin product such as polyethylene (PE) or polypropylene (PP). (Prior Art) Since polyethylene, polypropylene, etc. can be colored themselves, there is generally no need to paint them. However, for example, if an automobile bumper is obtained by molding the above-mentioned resin, it may be necessary to paint or color code a part of the automobile bumper in relation to other parts. . On the other hand, olefin resins have low surface energy and extremely weak coating film adhesion. Therefore, conventional methods have been to treat the surface of resin products with a chlorinated organic solvent such as trichlorethylene and then apply a primer, or to treat the surface with trichlorethylene as disclosed in JP-A-57-15870. A pre-painting treatment method has been proposed in which surface treatment is carried out using oxidizing low-temperature plasma treatment. (Problems to be Solved by the Invention) In the method described above, that is, the method of treating the surface of a polyolefin resin with a chlorinated organic solvent such as trichlorethylene, trichlorethylene is highly toxic and Careful attention must be paid to drainage and operational management.Furthermore, if the surface is treated with an organic solvent such as trichlorethylene, the surface of the resin product will become too rough, and if plasma treatment is applied, This results in so-called over-etching, which has the disadvantage of decreasing the peel strength of the coating film. (Means for Solving the Problems) In order to solve the above problems, the present invention uses a degreasing agent made of a water-soluble inorganic solvent instead of a chlorinated organic solvent such as trichlorethylene to produce polyolefin resin products. After degreasing the surface of O 2
The surface was treated with plasma to increase the adhesion of the coating on the surface of the resin product. (Function) By treating the surface of polyolefin resin products with a degreasing agent made of a water-soluble inorganic solvent, oils on the surface of the resin product can be easily removed, and problems caused by treatment with organic solvents can be avoided. In other words, over-etching due to extreme surface roughening can be avoided. In addition, wastewater treatment is easy because it only requires neutralizing the washing water, and there is no danger of air pollution or ignition caused by evaporation of organic solvents, and operational management is also easy. be.
In addition, there is no need to resupply the shortage due to evaporation, and so-called running costs are low. (Example) Examples of the present invention will be described below with reference to the accompanying drawings. In the examples, an automobile bumper is shown as a polyolefin resin product. First, in the present invention, as shown in FIG. 1, a molded automobile bumper 1 is immersed in a degreasing tank 2 to degrease the surface of the bumper 1. Here, the polyolefin resin constituting the bumper 1 includes, for example, polyethylene, polypropylene, polyethylene homopolymer, polypropylene homopolymer, ethylene vinyl acetate copolymer, ethylene acrylate copolymer, ethylene propylene copolymer, and a thermoplastic elastomer in a single substance or a mixture thereof. Examples include those mixed with inorganic fillers, glass fibers, etc. Further, as the degreasing agent, a degreasing agent made of a water-soluble inorganic solvent, specifically, sodium metasilicate or the like is used. In the example, the bumper 1 was suspended and supported by the hanger 3 and immersed in the degreasing tank 2, but a degreasing agent was sprayed onto the surface of the bumper 1 using a spray gun or the like. You can do it like this. When the degreasing process on the surface of the bumper 1 is completed in this way, as shown in FIG.
The bumper 1 surface is treated with O 2 plasma. Then, a polymer that does not contain oxygen, such as a polyolefin resin, incorporates a large amount of active oxygen radicals into the polymer as carbonyl bonds, increasing the surface energy and greatly increasing the adhesive strength of the coating film. The conditions for plasma processing here vary depending on the plasma processing tank, the shape of the product being processed, etc., but when using oxygen gas as the processing gas, the degree of vacuum is 0.3 to 5.0 Torr, and the frequency is 2450±.
It is preferable to use 10 MHz and a processing time of 5 to 300 seconds. Thereafter, as shown in FIG. 3, a two-component urethane paint 7 is applied as a top coat using a spray gun 6 to obtain a product. Next, specific experimental results are shown in a table and compared with conventional examples.
【表】
尚、実験におけるプラズマ処理の条件は以下
の通りである。
マイクロ波出力…2450MHz×1.5Kw
処理ガス…O2 97%、N2 3%
処理ガス流量…2/min
処理時間…20sec
圧力…0.8〜1.0Torr
また、塗膜剥離強度(Kg/cm)は、いわゆる
ピーリング強度と呼ばれ、焼付乾燥48時間後の
塗膜を1cm幅で30mm/分の速度で剥がすのに必
要な力を横型荷重測定機で測定したものであ
る。
〔表〕からも明らかなように本発明方法によ
れば、塗膜の剥離強度において、従来であれ
ば、予め接着性を向上させるためのプライマー
を塗布して下地処理したのと同程度の強度が得
られており、従来に比較して大幅に向上してい
ることが分る。
(発明の効果)
以上の説明から明らかな如く本発明に係る塗
装前処理方法によれば、水溶性の無機溶剤から
なる脱脂剤を用いてポリオレフイン系樹脂製品
の表面処理を行うようにしたので、後にプラズ
マ処理した場合にオーバーエツチングされるこ
とがなく、樹脂製品表面の塗膜接着力が向上す
る。また、トリクロルエチレン等を用いる場合
に比べ排水処理及び操業管理、安全管理等の面
においても極めて有利となる。[Table] The conditions for plasma treatment in the experiment are as follows. Microwave output…2450MHz×1.5Kw Processing gas…O 2 97%, N 2 3% Processing gas flow rate…2/min Processing time…20sec Pressure…0.8~1.0Torr Also, the coating peel strength (Kg/cm) is as follows: This is called peeling strength, and is the force required to peel off a 1cm wide coating at a speed of 30mm/min after 48 hours of baking drying, measured using a horizontal load measuring machine. As is clear from the table, according to the method of the present invention, the peel strength of the paint film is comparable to that of the conventional method, which was prepared by applying a primer in advance to improve adhesion. It can be seen that this is a significant improvement compared to the conventional method. (Effects of the Invention) As is clear from the above description, according to the painting pretreatment method according to the present invention, the surface treatment of polyolefin resin products is performed using a degreasing agent made of a water-soluble inorganic solvent. There is no over-etching when plasma treatment is performed later, and the adhesion of the coating film on the surface of the resin product is improved. Furthermore, it is extremely advantageous in terms of wastewater treatment, operational management, safety management, etc. compared to the case of using trichlorethylene or the like.
第1図は樹脂製品の脱脂工程を示す図、第2
図は脱脂処理された樹脂製品をプラズマ処理装
置へ搬入する図、第3図は樹脂製品に塗装を施
している図である。
尚、図面中1は樹脂製品であるバンパー、2
は脱脂槽、5はプラズマ処理装置である。
Figure 1 shows the degreasing process for resin products, Figure 2
The figure shows the degreased resin product being carried into the plasma processing apparatus, and FIG. 3 shows the resin product being painted. In addition, 1 in the drawing is a bumper which is a resin product, 2
5 is a degreasing tank, and 5 is a plasma processing device.
Claims (1)
の無機溶剤からなる脱脂剤によつて処理した
後、この樹脂製品を酸素ガスを主体とした処理
ガス雰囲気のプラズマ処理室にセツトし、次い
でプラズマ処理室内を減圧するとともにプラズ
マを発生せしめることで処理ガスを活性化せし
めて樹脂製品表面を処理するようにしたことを
特徴とする塗装前処理方法。1. After treating the surface of a polyolefin resin product with a degreasing agent made of a water-soluble inorganic solvent, the resin product is placed in a plasma treatment chamber with a treatment gas atmosphere mainly consisting of oxygen gas, and then the inside of the plasma treatment chamber is A pre-painting treatment method characterized in that the surface of a resin product is treated by activating a treatment gas by reducing the pressure and generating plasma.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP9053485A JPS61247740A (en) | 1985-04-26 | 1985-04-26 | Pre-painting treatment method |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP9053485A JPS61247740A (en) | 1985-04-26 | 1985-04-26 | Pre-painting treatment method |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS61247740A JPS61247740A (en) | 1986-11-05 |
| JPH0588262B2 true JPH0588262B2 (en) | 1993-12-21 |
Family
ID=14001074
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP9053485A Granted JPS61247740A (en) | 1985-04-26 | 1985-04-26 | Pre-painting treatment method |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS61247740A (en) |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5344462A (en) * | 1992-04-06 | 1994-09-06 | Plasma Plus | Gas plasma treatment for modification of surface wetting properties |
Family Cites Families (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS6034969B2 (en) * | 1980-06-30 | 1985-08-12 | 豊田合成株式会社 | Pre-painting treatment method for polyolefin products |
| JPS57158233A (en) * | 1981-03-26 | 1982-09-30 | Tokuyama Soda Co Ltd | Production of roughened polypropylene film |
-
1985
- 1985-04-26 JP JP9053485A patent/JPS61247740A/en active Granted
Also Published As
| Publication number | Publication date |
|---|---|
| JPS61247740A (en) | 1986-11-05 |
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