JPH032365A - Chemical resistant film - Google Patents
Chemical resistant filmInfo
- Publication number
- JPH032365A JPH032365A JP13284489A JP13284489A JPH032365A JP H032365 A JPH032365 A JP H032365A JP 13284489 A JP13284489 A JP 13284489A JP 13284489 A JP13284489 A JP 13284489A JP H032365 A JPH032365 A JP H032365A
- Authority
- JP
- Japan
- Prior art keywords
- film
- nitride
- base material
- ion plating
- mentioned
- 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.)
- Pending
Links
Landscapes
- Physical Vapour Deposition (AREA)
Abstract
Description
【発明の詳細な説明】
[産業上の利用分野]
本発明は酸、アルカリ等の薬品に対して抵抗性を有する
耐薬品性被膜に関する。DETAILED DESCRIPTION OF THE INVENTION [Field of Industrial Application] The present invention relates to a chemical-resistant coating that is resistant to chemicals such as acids and alkalis.
[従来技術]
耐摩耗性を向上させるためにイオンプレーティング法な
どによりIVa族金属の窒化物である窒化チタン(Ti
N)や窒化ジルコニウム(ZrN)などの被膜を材料表
面に被覆することは知られている。しかしながら、これ
らの金属窒化物は、高濃度の薬品、例えば塩酸、硫酸な
どの酸性のガスあるいは溶液中にさらされると、溶出す
ることが認められる。特に窒化物系のセラミックスは、
硝酸には容易に溶解してしまい、保護膜・耐摩耗性膜と
しての機能を失ってしまう。また湿式のめっきには、種
々の耐食性被膜があるが、上記の強酸には金めつき以外
保護膜として機能するものはない。さらに有機塗料の中
には、強酸に強いものもあるが、反面アルカリには弱い
という欠点を持っている。[Prior art] In order to improve wear resistance, titanium nitride (Ti
It is known to coat the surface of a material with a film such as N) or zirconium nitride (ZrN). However, it has been observed that these metal nitrides are eluted when exposed to highly concentrated chemicals such as acidic gases or solutions such as hydrochloric acid and sulfuric acid. In particular, nitride ceramics
It easily dissolves in nitric acid and loses its function as a protective film and wear-resistant film. Furthermore, although there are various corrosion-resistant coatings for wet plating, there is no such strong acid coating that functions as a protective coating other than gold plating. Furthermore, some organic paints are resistant to strong acids, but have the disadvantage of being weak to alkalis.
従って、従来、耐摩耗性と酸やアルカリ等の薬品に耐久
性のある保護被膜は開発されていなかった。Therefore, no protective coating has been developed that is wear resistant and resistant to chemicals such as acids and alkalis.
[発明が解決しようとする課題]
そこで本発明の目的は、上記問題点を解消するために高
濃度の酸やアルカリ等の薬品中でも耐摩耗性及び耐薬品
性等の機能を失わない被膜を提供することにある。[Problems to be Solved by the Invention] Therefore, an object of the present invention is to provide a coating that does not lose its wear resistance and chemical resistance even in chemicals such as highly concentrated acids and alkalis in order to solve the above problems. It's about doing.
[課題を解決するための手段]
上記目的を達成するために本発明は、ニオブ(Nb)お
よび/またはタンタル(Ta)がイオンプレーティング
法により窒化物として形成されてなる点に特徴がある。[Means for Solving the Problems] In order to achieve the above object, the present invention is characterized in that niobium (Nb) and/or tantalum (Ta) are formed as a nitride by an ion plating method.
[作用]
該被膜をイオンプレーティング法で形成する際、蒸発源
として金属Nbおよび金属Taを用いればよい。[Function] When forming the film by ion plating, metal Nb and metal Ta may be used as evaporation sources.
該被膜を形成する基材は特に限定されず、金属、合金、
プラスチック、セラミックおよびこれらの混合材料等を
挙げることができる。また、これらの基材の表面に別の
被膜、たとえば金属の窒化物、酸化物、炭化物等があら
かじめ形成されていても差し支えない。NbおよびTa
は該基材の表面に窒化物被膜として形成されねばならな
いが、窒化ニオブ(NbN)と窒化タンタル(TaN)
のいずれが下層となってもよく、またNbNとTaNが
混合された状態で被膜形成されてもよい。The base material on which the film is formed is not particularly limited, and may include metals, alloys,
Examples include plastics, ceramics, and mixed materials thereof. Further, another coating, such as a metal nitride, oxide, or carbide, may be previously formed on the surface of these base materials. Nb and Ta
must be formed as a nitride film on the surface of the substrate, but niobium nitride (NbN) and tantalum nitride (TaN)
Either of these may serve as the lower layer, or the film may be formed in a state where NbN and TaN are mixed.
本発明に用いるイオンプレーティング法は公知の装置を
用いればよいが、望ましくは真空アーク放電型が好適で
ある。該イオンプレーティング法でNb、 Taの窒化
物を形成させるときに用いる反応性ガスとしては、窒素
、アンモニアおよびこれらの混合ガスを挙げることがで
き、該反応性ガスをイオンプレーティング装置に導入し
つつ、該基材に負のバイアス電圧を印加し、生成した該
窒化物を該基材表面に形成すればよい。該被膜が耐久性
を有する薬品としては塩酸、硫酸、硝酸等の酸溶液と水
酸化カリウム、水酸化ナトリウム等のアルカリ溶液およ
びこれらのガス等を挙げることができる。For the ion plating method used in the present invention, any known apparatus may be used, but a vacuum arc discharge type is preferably used. Reactive gases used when forming Nb and Ta nitrides by the ion plating method include nitrogen, ammonia, and mixed gases thereof, and the reactive gases are introduced into the ion plating apparatus. At the same time, a negative bias voltage may be applied to the base material, and the generated nitride may be formed on the surface of the base material. Examples of chemicals with which the film is durable include acid solutions such as hydrochloric acid, sulfuric acid, and nitric acid, alkaline solutions such as potassium hydroxide and sodium hydroxide, and gases thereof.
[実施例]
601鳳×301厘、厚み3履鳳のステンレス鋼(SO
3304)基材を有機溶剤で洗浄し、真空アーク放電型
イオンプレーティング装置に取付けた。蒸発源としては
純度99.9%のNbターゲットを用いた。[Example] 601 mm x 301 mm, 3 mm thick stainless steel (SO
3304) The substrate was cleaned with an organic solvent and attached to a vacuum arc discharge type ion plating device. An Nb target with a purity of 99.9% was used as an evaporation source.
まず真空度をI X 10−’Torr以下にした後、
イオン衝撃により、基材の洗浄、加熱を行った。次に反
応性ガスとして窒素ガスを導入して、装置中圧力を30
mTorrとした。製膜では、Nbターゲットに100
Aの電流を流し、真空アーク放電でNbイオンを放出さ
せて、−300Vのバイアス電圧が印加された基材上に
NbNを45分間製膜した。さらに、基材を支持してい
た部分も被覆するため、支持する場所を変えて、45分
間製膜した。さらに、蒸発源として、純度99.9%の
Taターゲットを用い、ターゲットに流す電流値を15
0Aにした以外は、上記と同様におこない基材上にTa
Nを製膜した。First, after reducing the degree of vacuum to I x 10-'Torr or less,
The base material was cleaned and heated by ion bombardment. Next, nitrogen gas was introduced as a reactive gas, and the pressure in the device was increased to 30
mTorr. In film formation, 100% was applied to the Nb target.
A current was applied, Nb ions were released by vacuum arc discharge, and NbN was formed into a film for 45 minutes on the base material to which a bias voltage of -300V was applied. Furthermore, in order to cover the part that was supporting the base material, the supporting location was changed and the film was formed for 45 minutes. Furthermore, a Ta target with a purity of 99.9% was used as an evaporation source, and the current value flowing through the target was 15%.
The same procedure as above was carried out except that the Ta was applied to the base material.
A film of N was formed.
[比較例]
純度99.9%のTi及びZrをそれぞれターゲットと
し、電流値を90Aにした以外は実施例と同様にしてT
iNおよびZrNの被膜を製膜した。[Comparative example] Ti and Zr with a purity of 99.9% were used as targets, respectively, and T was produced in the same manner as in the example except that the current value was set to 90A.
Films of iN and ZrN were formed.
この被膜の耐薬品性を見るため、該被覆材をそれぞれ3
0枚ずつ、100%濃度の塩酸(Hcl)、硝酸(II
NO3) 、リン酸(+1.PO2)、酢酸(C)13
COOH)、アンモニア(N11.0I+)および50
%濃度の硫酸(lItSO*)、■θ%濃度の水酸化ナ
トリウム溶液の以上7種類の薬品中に室温で一週間浸清
させ、溶液中の被膜物質の金属の溶解量を誘導結合プラ
ズマ発光分光分析装置(ICP)により定量した。その
結果、第1表のような数値が得られた。In order to check the chemical resistance of this coating, each coating material was
0 sheets each, 100% concentration hydrochloric acid (Hcl), nitric acid (II
NO3), phosphoric acid (+1.PO2), acetic acid (C)13
COOH), ammonia (N11.0I+) and 50
% concentration of sulfuric acid (lItSO*) and ■θ% concentration of sodium hydroxide solution for one week at room temperature. It was quantified using an analyzer (ICP). As a result, the numerical values shown in Table 1 were obtained.
TiN、 ZrNは、塩酸、硝酸、硫酸などの酸にが
なりの量が溶出しているが、本発明のNbNは、塩酸、
硝酸、リン酸に対してわずかに溶出しているものの、そ
の量はTiNやZrNに比べると少ない。TiN and ZrN are eluted in large amounts by acids such as hydrochloric acid, nitric acid, and sulfuric acid, but the NbN of the present invention is
Although it is slightly eluted with nitric acid and phosphoric acid, the amount is smaller than that of TiN and ZrN.
さらにTaNは、はとんど溶出していない。Furthermore, TaN is hardly eluted.
第1表
[発明の効果]
以上のことから明らかなように、本発明は耐薬品性に優
れた被膜を提供するものであり、化学プラントなどの腐
食環境下での耐摩耗性を要求される部材に好適である。Table 1 [Effects of the Invention] As is clear from the above, the present invention provides a coating with excellent chemical resistance, which requires wear resistance in corrosive environments such as chemical plants. Suitable for parts.
Claims (1)
グ法により窒化物として形成されてなることを特徴とす
る耐薬品性被膜。A chemical-resistant coating characterized in that niobium and/or tantalum is formed as a nitride by an ion plating method.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP13284489A JPH032365A (en) | 1989-05-29 | 1989-05-29 | Chemical resistant film |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP13284489A JPH032365A (en) | 1989-05-29 | 1989-05-29 | Chemical resistant film |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| JPH032365A true JPH032365A (en) | 1991-01-08 |
Family
ID=15090839
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP13284489A Pending JPH032365A (en) | 1989-05-29 | 1989-05-29 | Chemical resistant film |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPH032365A (en) |
Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS5915984A (en) * | 1982-07-19 | 1984-01-27 | 日本電気株式会社 | Display panel driving circuit |
| JPS63192855A (en) * | 1987-02-04 | 1988-08-10 | Kawasaki Steel Corp | Production of low carbon steel sheet and stainless steel sheet coated with ceramic film having superior adhesion, uniformity and corrosion resistance |
-
1989
- 1989-05-29 JP JP13284489A patent/JPH032365A/en active Pending
Patent Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS5915984A (en) * | 1982-07-19 | 1984-01-27 | 日本電気株式会社 | Display panel driving circuit |
| JPS63192855A (en) * | 1987-02-04 | 1988-08-10 | Kawasaki Steel Corp | Production of low carbon steel sheet and stainless steel sheet coated with ceramic film having superior adhesion, uniformity and corrosion resistance |
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