JPS62151558A - Member having corrosion resistant alloy film - Google Patents

Member having corrosion resistant alloy film

Info

Publication number
JPS62151558A
JPS62151558A JP29042685A JP29042685A JPS62151558A JP S62151558 A JPS62151558 A JP S62151558A JP 29042685 A JP29042685 A JP 29042685A JP 29042685 A JP29042685 A JP 29042685A JP S62151558 A JPS62151558 A JP S62151558A
Authority
JP
Japan
Prior art keywords
film
base material
coating
resistant alloy
corrosion resistant
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
Application number
JP29042685A
Other languages
Japanese (ja)
Inventor
Toshihiko Odohira
尾土平 俊彦
Ryuichiro Ebara
江原 隆一郎
Tetsuyoshi Wada
哲義 和田
Hiroshi Nakajima
宏 中嶋
Yoshikiyo Nakagawa
義清 中川
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.)
Mitsubishi Heavy Industries Ltd
Original Assignee
Mitsubishi Heavy Industries 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 Mitsubishi Heavy Industries Ltd filed Critical Mitsubishi Heavy Industries Ltd
Priority to JP29042685A priority Critical patent/JPS62151558A/en
Publication of JPS62151558A publication Critical patent/JPS62151558A/en
Pending legal-status Critical Current

Links

Landscapes

  • Turbine Rotor Nozzle Sealing (AREA)
  • Laminated Bodies (AREA)
  • Physical Vapour Deposition (AREA)

Abstract

PURPOSE:To provide a titled member which prevents the material deterioration of the member by the high temp. during the formation of the film and has the improved adhesiveness of the film by having the corrosion resistant alloy film essentially consisting of Co, Cr and W by vacuum deposition on the surface of a base material. CONSTITUTION:An alloy essentially consisting of Co, Cr and W is evaporated in the vacuum in which the partial pressure of Ar and the partial pressure of C2H2 are respectively specified to deposit the vapor of the above-mentioned alloy by ion plating in the vacuum on the surface of the base material (e.g.; SUS410J-1) heated and held to and at 500 deg.C. the film consisting of, for example, Co and the balance 28wt% Cr, 5.1wt% W and 0.9wt% Co is coated on the surface of the base material. The material deterioration of the base material by the formation of the corrosion resistant alloy film is thereby prevented and the adhesiveness of said film is improved. As a result, the life of the member having the corrosion resistant alloy film is considerably extended.

Description

【発明の詳細な説明】 (産業上の利用分野) 本発明はCo 、 Or 、 Wを主成分とする耐浸食
性合金被膜を有する部材に関する。
DETAILED DESCRIPTION OF THE INVENTION (Field of Industrial Application) The present invention relates to a member having an erosion-resistant alloy coating containing Co, Or, and W as main components.

(従来の技術) 従来、蒸気タービンのブレード、パルグミルノスクリュ
ー、工/ヂンバルプ等の機械部品の表面は、例えば、ブ
レードでは湿)蒸気によるドレンエロージョン、スクリ
ュー−p ハ/l/ 7” ハg食と摩耗のように浸食
(エロージョン)作用によって劣化している。この劣化
の対策として、従来は機械部品の表面に耐浸食性に優れ
たGo。
(Prior art) Conventionally, the surfaces of mechanical parts such as steam turbine blades, pargum screws, and mechanical parts have been exposed to condensate erosion due to steam (for example, wet blades), screw erosion, etc. The deterioration occurs due to the action of erosion, such as corrosion and wear.As a countermeasure to this deterioration, conventionally, Go, which has excellent erosion resistance, was applied to the surfaces of mechanical parts.

(jr、 Wを主成分とする合金板をロウ付は法によっ
て、張シ付けたり、前記合金成分の棒や粉末を肉盛溶接
法や、溶射法によって初覆し、対応している。
(Jr, W-based alloy plates are brazed or stretched using a brazing method, or bars or powder of the alloy components are initially overlaid using overlay welding or thermal spraying methods.

従来のロウ付は法ならび肉盛溶接法、溶射法によって被
αさnた部材には以下のような問題がある。即ち、上記
各施工法に2いては、金属である基材ならびに被覆材が
溶融する程の高温加熱によって施工が行わnておシ、こ
のために、基材の材質によっては疲労限が低下して強度
設計上の制約が厳しくなる。また、基材と被機材との合
金層において成分金属元素の濃度偏析が生じ、靭性の劣
化や強度低下を生じることがある。さらに、上記施工法
は殆んどの場合手作業で行わnておシ、多大な労力が必
要であり、品質性能のバラツキが生じて、製品の均質性
に欠ける問題がある。
There are the following problems with parts that have been subjected to conventional brazing, overlay welding, and thermal spraying. That is, in each of the above-mentioned construction methods, the construction is performed by heating at a high enough temperature that the base material and coating material, which are metals, melt.As a result, the fatigue limit may be lowered depending on the material of the base material. Therefore, restrictions on strength design become stricter. In addition, concentration segregation of component metal elements may occur in the alloy layer between the base material and the substrate, resulting in deterioration of toughness and strength. Furthermore, the construction method described above is carried out manually in most cases and requires a great deal of labor, resulting in variations in quality performance and a problem of lack of homogeneity of the product.

(発明が解決しようとする問題点〕 本発明は従来の耐浸食性合金被膜を有する部材の欠点を
解消し、被膜形成時の高温による部材の材質的劣化を防
止し、かつ、級換の密着性を向上させた耐浸食性合金被
膜を有する部材を提供しようとするものである。
(Problems to be Solved by the Invention) The present invention eliminates the drawbacks of conventional members having corrosion-resistant alloy coatings, prevents material deterioration of the member due to high temperatures during coating formation, and improves adhesion during grading. The object of the present invention is to provide a member having an corrosion-resistant alloy coating with improved properties.

(問題点を解決するための手段) 本発明は基材表面に真空蒸着によって形成したCo 、
 Cr 、’Wを主成分とする耐浸食性合金被膜を有す
ることを特徴とする部材、及び基材表面に真空蒸着によ
って形成したOr  被膜と、該被膜の上に真空蒸着に
よp形成したCo、Or、Wを主成分とする耐浸食性合
金被膜とを有することを特徴とする部材である。
(Means for Solving the Problems) The present invention provides Co formed on the surface of a base material by vacuum evaporation,
A member characterized by having an erosion-resistant alloy coating containing Cr, 'W as the main components, an Or coating formed on the surface of the base material by vacuum evaporation, and a Co coating formed on the coating by vacuum evaporation. , Or, and an erosion-resistant alloy coating containing W as main components.

(作用〕 本発明は真空蒸着法により沙展の形成を行なうために、
基材は例えば、500C程度の比較的低温で加熱を行な
うことが可能となシ、部材の強度低下を来すことがない
。また、被膜形成をする基材表面が処理前に不活性な酸
化i膜を形成していたシ被膜形成の真空雰囲気中の水蒸
気分圧が高い場合には活性に仕上げ九基材表面が酸化さ
れ不活性になることかめシ、その結果、耐浸食性合金被
膜の密着性が低下することがあるが、酸素との親和性の
弛いOr  破膜を基材表面に形成することにより、仮
に基材表面が不活性な酸化被膜を形成している場合に2
いても、基材とOr  被膜との強い結合性を確保でき
、更には、Cr被験のOrは耐浸食性合金被膜の構成成
分の一部であるために、両被膜の結合性も強いものとな
る。
(Function) In order to form a sand layer by vacuum evaporation method, the present invention has the following steps:
The base material can be heated at a relatively low temperature of about 500 C, for example, without causing a decrease in the strength of the member. In addition, if the surface of the substrate on which the film is to be formed has formed an inactive oxide film before the treatment, and the partial pressure of water vapor in the vacuum atmosphere during film formation is high, the surface of the substrate will be oxidized. The adhesion of the corrosion-resistant alloy coating may decrease as a result of becoming inert, but by forming a broken film on the surface of the substrate that has a loose affinity for oxygen, 2 when the material surface forms an inert oxide film.
However, since the Or in the Cr test is a component of the corrosion-resistant alloy coating, the bond between the two coatings is also strong. Become.

(実施例1) Are圧3 X 10  Torr 、 C2H2分圧
1x10″″4Torr  で形成される真空中におい
てQo、Or、Wを主成分とする合金を蒸発させ、50
0Cに加熱保持した基材(SUS 410 J −1)
の表面に上記合金の蒸気をイオンブレーティングによっ
て真空蒸着し、Co、残部、 Or 28 wt%、 
W 5,1wt%、C0,9wt%の被膜をコーティン
グした。
(Example 1) An alloy mainly composed of Qo, Or, and W was evaporated in a vacuum formed with an Are pressure of 3 x 10 Torr and a C2H2 partial pressure of 1 x 10''4 Torr.
Base material heated and maintained at 0C (SUS 410 J-1)
Vapor of the above alloy was vacuum deposited on the surface of the alloy by ion blasting, and Co, the balance, Or 28 wt%,
A film containing 5.1 wt% W and 0.9 wt% CO was coated.

第1図は基材であるSUS 410 J −1の無処理
材とこの材料に本発明コーティングを施工した場合の基
材ならびに従来法のロウ付法を施工した場合の基材の疲
労強度を比較した結果である。なお、従来法は、真空蒸
着によシ薔模した被膜と同一組成の厚さ0.81)の板
材を、5US410J−1の基材表面に850Cに加熱
してロウ付けを行なった。第1図では無処理材と本発明
は変化がないが、従来法は特に疲労強度が低下し、材質
的劣化が生じていることが判明した。
Figure 1 compares the fatigue strength of the untreated base material SUS 410 J-1, the base material when the coating of the present invention is applied to this material, and the base material when the conventional brazing method is applied. This is the result. In the conventional method, a plate material having a thickness of 0.81 mm and having the same composition as the vacuum-deposited rose-like coating was brazed onto the surface of a 5US410J-1 base material by heating it to 850C. In FIG. 1, there is no difference between the untreated material and the present invention, but it was found that the conventional method had a particularly low fatigue strength and material deterioration.

同様に、第1表はキャビテーションエロージョン試験に
よる。コーティング表向の重量減少量を測定した結果で
ある。なお、キャビテτジョンエロージョン試騒は水中
にて周波数18.3KRz掘幅40μm の超音波を発
振させて気泡を発生させ、この気泡を破膜表面に衝突さ
せて被膜の剥離a度を試験するもので破膜の密着性試験
の18!である。このデータにおいても本発明法は無処
理のGo −Or −W合金に匹敵する良好な結果が得
らnた。
Similarly, Table 1 is from the cavitation erosion test. These are the results of measuring the amount of weight loss on the surface of the coating. In addition, the cavity τ John erosion test is a test in which an ultrasonic wave with a frequency of 18.3 KRz and a depth of 40 μm is oscillated underwater to generate bubbles, and the bubbles collide with the surface of the broken membrane to test the degree of peeling of the membrane. 18 of the ruptured membrane adhesion test! It is. In this data as well, the method of the present invention yielded good results comparable to the untreated Go-Or-W alloy.

第1表 単位(ダ) (実施例2) 第2図は本発明のコーティング被膜構成の1fl k示
す。戻りち1は被コーテイング材であり、2はCjrの
コーティング抜脱であシ、3はGo。
Table 1 Unit (Da) (Example 2) FIG. 2 shows 1flk of the coating structure of the present invention. Return 1 is the material to be coated, 2 is the Cjr coating removal, and 3 is Go.

Or、W、Fe  Cを含有する合金の耐浸食性コーテ
ィング被膜である。抜脱2および被膜、3のコーティン
グは次のように行なった。
It is an erosion-resistant coating film of an alloy containing Or, W, Fe C. Extraction 2 and coating 3 were performed as follows.

圧力2X10Torrの真空中にあ・いて、5US4j
OJ−1の被コーテイング材1を5000に加熱保持し
、この真空中にAr  ガスを供給し、このAr  ガ
スの分圧を3X10Torrになるよう保持して、Or
  を加熱蒸発させ、イオンプレ−ティングによって厚
さ6μmのOrのコーティング破膜2を被コーテイング
材1の表面に形成した。続いてCr  の蒸発を停止し
、直ちにこの真空中1CCHを供給し、このC2H2の
分圧を1X 10−”Torrになるよう保持し、Or
  の蒸発、Wの蒸発、COとFe成分を調整した合金
とからCOとFeを蒸発させそれぞれの蒸発量を調節し
て、前記被膜2の表面にイオンブレーティングによって
被膜3を形成した。この被膜3の合金組成はCio残部
、Cr 28 wt%、W 5.5 wt%、Fe1.
0wt%、C2H2の放電によって形成したCI、4w
t%で形成されておシ厚さは10μm である。
5US4j in a vacuum with a pressure of 2X10 Torr
The material to be coated 1 of OJ-1 is heated and maintained at 5000℃, Ar gas is supplied into this vacuum, and the partial pressure of this Ar gas is maintained at 3X10 Torr.
was heated and evaporated, and a 6 μm thick Or coating rupture film 2 was formed on the surface of the material to be coated 1 by ion plating. Subsequently, evaporation of Cr is stopped, 1CCH is immediately supplied in this vacuum, the partial pressure of this C2H2 is maintained at 1X 10-'' Torr, and Or
A coating 3 was formed on the surface of the coating 2 by ion blasting by evaporating CO and Fe from an alloy with adjusted CO and Fe components and adjusting the amount of each evaporation. The alloy composition of this coating 3 is Cio balance, Cr 28 wt%, W 5.5 wt%, Fe1.
CI formed by discharging 0wt%, C2H2, 4w
t% and has a thickness of 10 μm.

第3図は以上のような2層コーティング被膜Aと比較例
としてOr  コーティング被&2が存在しない被膜3
と同組成のコーティング被膜10μm の厚さのamB
、  さらに比較例として被膜3と同組成を溶製で製作
した合金Cの各々のキャビテーションエロージョン試験
の結果を示す。この結果によnば本発明Aは合金Cと同
程度の重量減少を呈し、優れた耐浸食性を示しているが
、比較例Bは沙腹自体の浸食はA、 0と同程度である
が破膜の密着力が弱く剥離したため、被コーテイング材
が浸食された。なお、浸食区数は純水中にコーチインク
w!腹部を浸漬し、これに周波数I B、5 Kム、振
幅40μm の超音波振動を純水を介して与え、その時
に発生する気泡が被膜部の表面に衝突し、破裂すること
によるキャビテーションエロージョン′Ijr:測定す
るものである。
Figure 3 shows the above two-layer coating film A and, as a comparative example, film 3 in which Or coating film &2 does not exist.
A coating film with the same composition as amB with a thickness of 10 μm
Furthermore, as a comparative example, the results of cavitation erosion tests are shown for alloy C, which was produced by melting and having the same composition as coating 3. According to the results, Invention A exhibits a weight loss comparable to that of Alloy C and exhibits excellent corrosion resistance, but Comparative Example B exhibits the same degree of erosion of the sandbari itself as Alloy A. However, the adhesion of the ruptured membrane was weak and it peeled off, resulting in erosion of the coated material. In addition, the number of eroded areas is coach ink in pure water lol! Cavitation erosion occurs when the abdomen is immersed and subjected to ultrasonic vibrations with a frequency of 5 Km and an amplitude of 40 μm through pure water, and the bubbles generated at that time collide with the surface of the coating and burst. Ijr: Something to be measured.

(発明の効果) 本発明は、上記構成を採用することによシ、耐浸食性合
金破膜の形成による基材の材質的劣化が防止され、該被
膜の密着性が向上し、その結果として、耐浸食性合金被
膜を有する部材の寿命を大巾に延長することができた。
(Effects of the Invention) By adopting the above configuration, the present invention prevents material deterioration of the base material due to the formation of an erosion-resistant alloy fractured film, improves the adhesion of the film, and as a result, , it was possible to significantly extend the life of a member having an erosion-resistant alloy coating.

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

第1図は本発明の1実施例と比較例の部材についての疲
労強度試験結果の図、第2図は本発明の1つの被膜構成
例を示す図、第3図は本発明の実施例と比較例の部材に
ついてのキャビテーションエロージョン試験結果の図で
ある。 復代理人 内 1)  明 復代理人 萩 原 亮 − 復代理人 安 西 篤 夫 曲(ず2・力(K!j/mす 貢 晋 減/l)(mg)
Fig. 1 is a diagram showing fatigue strength test results for members of an embodiment of the present invention and a comparative example, Fig. 2 is a diagram showing an example of a coating structure of the present invention, and Fig. 3 is a diagram showing an example of the structure of a coating of the present invention. It is a figure of the cavitation erosion test result about the member of a comparative example. Sub-Agents 1) Meifuku Agent Ryo Hagiwara - Sub-Agent Atsushi Anzai Fukyoku (Z2・Power (K!j/msu Mitsugu Susumu/l) (mg)

Claims (2)

【特許請求の範囲】[Claims] (1)基材表面に真空蒸着によって形成したCo、Cr
、Wを主成分とする耐浸食性合金被膜を有することを特
徴とする部材。
(1) Co, Cr formed on the surface of the base material by vacuum deposition
, a member characterized by having an erosion-resistant alloy coating containing W as a main component.
(2)基材表面に真空蒸着により形成したCr被膜と、
該被膜の上に真空蒸着により形成したCo、Cr、Wを
主成分とする耐浸食性合金被膜とを有することを特徴と
する部材。
(2) a Cr coating formed on the surface of the base material by vacuum deposition;
A member characterized in that it has an erosion-resistant alloy coating mainly composed of Co, Cr, and W formed by vacuum deposition on the coating.
JP29042685A 1985-12-25 1985-12-25 Member having corrosion resistant alloy film Pending JPS62151558A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP29042685A JPS62151558A (en) 1985-12-25 1985-12-25 Member having corrosion resistant alloy film

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP29042685A JPS62151558A (en) 1985-12-25 1985-12-25 Member having corrosion resistant alloy film

Publications (1)

Publication Number Publication Date
JPS62151558A true JPS62151558A (en) 1987-07-06

Family

ID=17755879

Family Applications (1)

Application Number Title Priority Date Filing Date
JP29042685A Pending JPS62151558A (en) 1985-12-25 1985-12-25 Member having corrosion resistant alloy film

Country Status (1)

Country Link
JP (1) JPS62151558A (en)

Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS57202302A (en) * 1981-06-08 1982-12-11 Mitsubishi Acetate Co Ltd Preparation of carrageenan
JPS5898047A (en) * 1981-12-09 1983-06-10 Mitsubishi Acetate Co Ltd Preparation of carrageenan
JPS5996102A (en) * 1982-11-24 1984-06-02 Mitsubishi Acetate Co Ltd Production of carrageenan
JPS59113002A (en) * 1982-12-21 1984-06-29 Mitsubishi Acetate Co Ltd Production of carrageenan

Patent Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS57202302A (en) * 1981-06-08 1982-12-11 Mitsubishi Acetate Co Ltd Preparation of carrageenan
JPS5898047A (en) * 1981-12-09 1983-06-10 Mitsubishi Acetate Co Ltd Preparation of carrageenan
JPS5996102A (en) * 1982-11-24 1984-06-02 Mitsubishi Acetate Co Ltd Production of carrageenan
JPS59113002A (en) * 1982-12-21 1984-06-29 Mitsubishi Acetate Co Ltd Production of carrageenan

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