JPS604756B2 - Fluororesin coating method - Google Patents

Fluororesin coating method

Info

Publication number
JPS604756B2
JPS604756B2 JP3501480A JP3501480A JPS604756B2 JP S604756 B2 JPS604756 B2 JP S604756B2 JP 3501480 A JP3501480 A JP 3501480A JP 3501480 A JP3501480 A JP 3501480A JP S604756 B2 JPS604756 B2 JP S604756B2
Authority
JP
Japan
Prior art keywords
layer
ceramic
fluororesin
film
base material
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
Application number
JP3501480A
Other languages
Japanese (ja)
Other versions
JPS56130276A (en
Inventor
幸治 船越
恒雄 柴田
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.)
Panasonic Holdings Corp
Original Assignee
Matsushita Electric Industrial 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 Matsushita Electric Industrial Co Ltd filed Critical Matsushita Electric Industrial Co Ltd
Priority to JP3501480A priority Critical patent/JPS604756B2/en
Publication of JPS56130276A publication Critical patent/JPS56130276A/en
Publication of JPS604756B2 publication Critical patent/JPS604756B2/en
Expired legal-status Critical Current

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Description

【発明の詳細な説明】 本発明はアルミニウム基材表面に溶融贋霧法を用いてセ
ラミックと樹脂の混合皮膜を形成し、この皮膜内に含ま
れる樹脂を加熱分解して除去することにより弗素樹脂コ
ーティングに適した下地処理を形成する方法に関するも
のである。
Detailed Description of the Invention The present invention forms a mixed film of ceramic and resin on the surface of an aluminum base material using a melt atomization method, and removes the resin contained in this film by thermal decomposition. The present invention relates to a method for forming a base treatment suitable for coating.

弗素樹脂皮膜は他の高分子材料皮膜と比較して、耐熱性
、耐食性、非粘着性、低摩擦性、電気絶縁性が優れ非常
に広範な分野でこれらの特性を生かした用い方がなされ
ている。
Fluororesin coatings have superior heat resistance, corrosion resistance, non-adhesiveness, low friction, and electrical insulation properties compared to other polymeric material coatings, and are used in a wide range of fields to take advantage of these properties. There is.

例えば家庭用機器としてホットプレート、アイロンなど
では耐熱性、非粘着性、低摩擦性が生かされており、軸
受け表面では低摩擦性をうまく活用している。弗素樹脂
の中でもポリ四弗化エチレンは他のポリ三弗化塩化エチ
レン、四弗化エチレン−6発化プロピレン共重合体等と
比較して上記の特性が優れており、非常によく用いられ
ているが、これらのポリ四弗化エチレンをはじめとする
発素樹脂は低摩擦性を有する反面、接着力が弱いという
短所を持つている。また弗素樹脂自体硬度が低く、機器
として長期間使用した場合皮膜が摩耗したり金筑などで
摩擦すると皮膜が破れ金属素地が露出し、基材の腐食・
皮膜剥離を生じる。これに対し、弗素樹脂と基材の接着
性を向上させ、かつ弗素樹脂皮膜の摩耗を少なくするた
ため次の様な処理が通常なされている。
For example, household appliances such as hot plates and irons take advantage of their heat resistance, non-adhesiveness, and low friction properties, and bearing surfaces make good use of their low friction properties. Among fluororesins, polytetrafluoroethylene has superior properties as compared to other polytrifluorochloroethylenes, tetrafluoroethylene-6-propylene copolymers, etc., and is very commonly used. However, although these resins such as polytetrafluoroethylene have low friction properties, they have the disadvantage of weak adhesive strength. In addition, fluororesin itself has low hardness, and when used as a device for a long period of time, the coating will wear out, or if it is rubbed against metal chips, the coating will tear and the metal base will be exposed, causing corrosion of the base material.
Causes film peeling. In order to improve the adhesion between the fluororesin and the base material and to reduce the wear of the fluororesin film, the following treatments are usually carried out.

基材との接着性をあげる手段としては、塩酸処理等によ
る化学的エッチング法とサンドブラストの様な機械的方
法とがある。
Means for improving adhesion to the base material include chemical etching methods such as hydrochloric acid treatment and mechanical methods such as sandblasting.

ところが化学的処理方法の場合には、例えば塩酸処理の
様に酸が基村を腐食させるため処理後に十分な洗浄を必
要とし、特にダィカスト製基材の場合には巣内部等に腐
食液が浸透し、洗浄後も腐食の進行が生じたりしやすい
However, in the case of chemical treatment methods, such as hydrochloric acid treatment, the acid corrodes the base material, so sufficient cleaning is required after treatment, and especially in the case of die-cast base materials, the corrosive liquid may penetrate into the cavities, etc. However, corrosion is likely to continue even after cleaning.

また腐食しやすい金属を鋳込んだダィカスト基材の場合
、酸処理を行なうに当って鋳込まれた金属の露出部が処
理液に触れぬようにシールしなければならないため工程
が複雑になる欠点がある。また、機械的処理を施した場
合基板表面に極度の凹凸をもたせることは困難であり弗
素樹脂皮膜に対する技描効果に限度がある。
In addition, in the case of die-cast base materials in which metals that are easily corroded are cast, the process becomes complicated because the exposed parts of the cast metal must be sealed so that they do not come into contact with the treatment liquid during acid treatment. There is. Further, when mechanical treatment is applied, it is difficult to make the substrate surface extremely uneven, and there is a limit to the technical drawing effect on the fluororesin film.

従って基材と皮膜との接着性を良くするためにクロム酸
塩または酸化鉄等のバインダーを含むプラィマー層の前
処理コーティングを通常行っている。一方、皮膜の機械
的耐摩耗性を向上させる手段として、兼素樹脂皮膜の下
地処理にセラミック、硬質金属の溶射皮膜層を設けたり
、アルミニウム基材表面にアルマイト層を設け、このア
ルマイト層の割れ目内に弗素樹脂を喰い込ませたりして
いる。しかしながら、溶射皮膜層を設ける方法では、溶
射層表面の凹凸部に弗素樹脂層を食い込ませているが、
単に没描効果だけでは接着力が弱く溶射層と弗素樹脂層
の間にプラィマー層を必要とする。
Therefore, a pretreatment coating of a primer layer containing a binder such as chromate or iron oxide is usually used to improve the adhesion of the coating to the substrate. On the other hand, as a means to improve the mechanical abrasion resistance of the coating, a ceramic or hard metal thermal spray coating layer is provided as a base treatment for the dual-component resin coating, or an alumite layer is provided on the surface of the aluminum base material, and the cracks in this alumite layer are Fluorine resin is embedded inside. However, in the method of providing a thermal sprayed coating layer, the fluororesin layer digs into the irregularities on the surface of the thermal sprayed layer.
A mere immersion effect has weak adhesion and requires a primer layer between the sprayed layer and the fluororesin layer.

またアルミニウム表面を陽極酸化させ硬質アルマイトを
形成させる方法は発素樹脂を接着させる方法として硬質
アルマイト層に熱衝撃を加えクラックを生じさせ、この
クラック内部に※素樹脂ディスパージョンを合浸してい
るがこの含浸工程に手間を要する。
In addition, the method of anodizing the aluminum surface to form hard alumite is a method of adhering the emitting resin by applying thermal shock to the hard alumite layer to create cracks, and then injecting the base resin dispersion into the inside of these cracks. This impregnation process requires time and effort.

また皮膜厚も厚くするのに限度がある。上記の如く弗素
樹脂被覆を行う場合、特に耐摩耗性を要求される使用条
件においては、被覆のための下地処理工程および被覆工
程が複雑になるのが現状である。
There is also a limit to how thick the film can be made. When coating with a fluororesin as described above, the current situation is that the base preparation process and coating process for coating are complicated, especially under usage conditions that require abrasion resistance.

これに対し本発明は弗素樹脂と基材との接着性が良く、
かつ製造工程的にも簡易な被覆方法を提供するものであ
る。以下に被覆方法および構成を説明する。
In contrast, the present invention has good adhesion between the fluororesin and the base material,
Moreover, it provides a coating method that is simple in terms of manufacturing process. The coating method and structure will be explained below.

第1図に示す如く基材1表面をブラスト処理し、その後
セラミック材料を用いた溶射層2を形成する。ブラスト
材粒度としては#8鼠蓮度のものが表面の凹凸として適
当であり、溶射材としては種々の材料が可能だが特にA
I203−Ti02成分のものが基材との密着性、コス
トの点で適している。一例としてAI203−Ti02
を用いプラズマ溶射を行なった場合の熔射条件は、アー
ク電圧40V、アーク電流1000A、アークガス(A
r十日e)、粉末供給速度3夕/秒であり、皮膜厚は2
0りの前後が望ましい。このAI203−Ti02層の
上にセラミックと有機樹脂の混在する溶射層3を形成す
る。この時のセラミック材は熱膨張係数を合わせるため
に前記のセラミック層の材料と同一のものを用いる。有
機材料としてはエポキシ、ポリエチレン、ナイロン、ポ
リァミド等を用いる。セラミックと有機材料とでは融点
が異なるためこの両者を混合して同時に港射することは
できず個々に溶融させ頃霧させなければならない。プラ
ズマ溶射を用いた場合では、溶射ガンを2台設置し、セ
ラミックと有機樹脂を各々の溶射ガンから同時に曙覆さ
せる。セラミックと有機樹脂の混合皮膜内の有機樹脂比
率は5〜20%程度が適切であり有機樹脂が多くなると
皮膜の密着性が悪くなる。皮膜厚はN203一Ti02
層と同様20ム肌程度で厚くすると剥離を生ずる。この
セラミック・有機樹脂の混合港射層を形成した後、基板
全体を加熱処理し有機樹脂を加熱分解し気化させる。加
熱温度は高温な程、樹脂の分解は促進されるが基材の融
点および溶射層と基材の熱膨張の点から制限される。基
村をAI、セラミック材にAI203一Ti02を用い
た場合400〜500qoが最適温度である。この加熱
処理により、溶射層内の樹脂分4は分解され層内が多孔
質5となる。この多孔質5は混合綾射層3表面にも無数
にでき表面を没樹効果の優れた凹凸にする。加熱分解後
に若干樹脂の残留物が付着しているがエアーで表面残留
物を除去する。その後、弗素樹脂ディスパージョンを塗
布し、焼成することにより弗素樹脂皮膜6を形成する。
なお第1図において基材1をブラストした後、その上に
セラミック溶射層2を形成し、さらにその上にセラミッ
ク・有機材料の混合層3を設ける。
As shown in FIG. 1, the surface of the base material 1 is subjected to a blast treatment, and then a thermal spray layer 2 made of a ceramic material is formed. The particle size of the blasting material is #8, which is suitable for the roughness of the surface, and various materials are possible as the thermal spraying material, but especially A.
The I203-Ti02 component is suitable in terms of adhesion to the base material and cost. As an example AI203-Ti02
The conditions for plasma spraying are: arc voltage 40V, arc current 1000A, arc gas (A
r10daye), the powder supply rate was 3 m/sec, and the film thickness was 2
Preferably around 0. A sprayed layer 3 containing a mixture of ceramic and organic resin is formed on this AI203-Ti02 layer. The ceramic material at this time is the same as that of the ceramic layer described above in order to match the coefficient of thermal expansion. Epoxy, polyethylene, nylon, polyamide, etc. are used as the organic material. Since ceramic and organic materials have different melting points, they cannot be mixed and sprayed at the same time, but must be melted individually and then atomized. When plasma spraying is used, two spray guns are installed, and the ceramic and organic resin are simultaneously sprayed from each spray gun. The appropriate ratio of organic resin in the mixed film of ceramic and organic resin is about 5 to 20%, and as the amount of organic resin increases, the adhesion of the film deteriorates. Film thickness is N203-Ti02
As with the layer, if the thickness is about 20 mm, peeling will occur. After forming this mixed radiation layer of ceramic and organic resin, the entire substrate is heat-treated to thermally decompose and vaporize the organic resin. The higher the heating temperature, the more accelerated the decomposition of the resin, but it is limited by the melting point of the base material and the thermal expansion of the sprayed layer and the base material. When Motomura is made of AI and the ceramic material is made of AI203-Ti02, the optimum temperature is 400 to 500 qo. By this heat treatment, the resin component 4 in the sprayed layer is decomposed and the layer becomes porous 5. This porous material 5 is also formed on the surface of the mixed traverse layer 3, making the surface uneven with an excellent tree-killing effect. After thermal decomposition, some resin residue remains on the surface, but remove it with air. Thereafter, a fluororesin dispersion is applied and fired to form a fluororesin film 6.
In FIG. 1, after the base material 1 is blasted, a ceramic sprayed layer 2 is formed thereon, and a mixed layer 3 of ceramic and organic material is further provided thereon.

4は混合層内の有機材料を示す。4 indicates the organic material in the mixed layer.

セラミック層は基材と混合層との間に緩衝層として密着
性をあげるために設けられている。第2図は第1図の基
板全体を加熱処理し、混合層3内の樹脂を除去させて空
孔5を作った後、弗素樹脂皮膜6を形成したものである
。この加熱処理により混合層表面に樹脂の除去した跡の
無数の凹凸ができ、弗素樹脂の接着力を強固にしている
。本被覆方法を用いれば、化学的エッチングおよび陽極
酸化にみられる様な基材の腐食促進作用が全くなく、か
つプラィマー層を必要としないで接着性の良い耐摩耗皮
膜を得ることができる。
The ceramic layer is provided as a buffer layer between the base material and the mixed layer to improve adhesion. In FIG. 2, the entire substrate shown in FIG. 1 is heat-treated to remove the resin in the mixed layer 3 and create pores 5, and then a fluororesin film 6 is formed. This heat treatment creates numerous irregularities on the surface of the mixed layer, which are traces of resin removal, and strengthens the adhesive strength of the fluororesin. By using this coating method, it is possible to obtain a wear-resistant coating with good adhesion without causing any corrosion-promoting effect on the base material as seen in chemical etching and anodizing, and without requiring a primer layer.

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

第1図は本発明による方法による加熱処理前の基村の断
面図、第2図は同弗素樹脂被覆し加熱処理後の基材の断
面図である。 1……基材、2,3……溶射層、4……樹脂分、5・・
・・・・多孔質、6・・・・・・弗素樹脂皮膜。
FIG. 1 is a sectional view of a base material before heat treatment according to the method of the present invention, and FIG. 2 is a sectional view of a base material coated with the same fluororesin and after heat treatment. 1... Base material, 2, 3... Thermal spray layer, 4... Resin component, 5...
...Porous, 6...Fluororesin film.

Claims (1)

【特許請求の範囲】[Claims] 1 粗面化された金属表面に硬質セラミツクを溶融噴霧
して皮膜層を形成し、この皮膜上に有機材料とセラミツ
クの混在した皮膜層を溶融噴霧により形成した後、この
皮膜内の有機材料が熱分解する温度以上で加熱し、表面
の熱分解物を除去した後、多孔質となったセラミツク表
面に弗素樹脂デイスパージヨンを塗布・焼成させたこと
を特徴とする弗素樹脂被覆方法。
1. After forming a film layer by melt-spraying hard ceramic on a roughened metal surface, and forming a film layer containing a mixture of organic material and ceramic on this film by melt-spraying, the organic material in this film is A fluororesin coating method characterized by heating at a temperature above pyrolysis to remove pyrolyzed products on the surface, then applying and firing a fluororesin dispersion onto the porous ceramic surface.
JP3501480A 1980-03-18 1980-03-18 Fluororesin coating method Expired JPS604756B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP3501480A JPS604756B2 (en) 1980-03-18 1980-03-18 Fluororesin coating method

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP3501480A JPS604756B2 (en) 1980-03-18 1980-03-18 Fluororesin coating method

Publications (2)

Publication Number Publication Date
JPS56130276A JPS56130276A (en) 1981-10-13
JPS604756B2 true JPS604756B2 (en) 1985-02-06

Family

ID=12430210

Family Applications (1)

Application Number Title Priority Date Filing Date
JP3501480A Expired JPS604756B2 (en) 1980-03-18 1980-03-18 Fluororesin coating method

Country Status (1)

Country Link
JP (1) JPS604756B2 (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH0540310Y2 (en) * 1985-12-06 1993-10-13

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH0540310Y2 (en) * 1985-12-06 1993-10-13

Also Published As

Publication number Publication date
JPS56130276A (en) 1981-10-13

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