JP2547020B2 - High corrosion resistance amorphous nickel alloy - Google Patents

High corrosion resistance amorphous nickel alloy

Info

Publication number
JP2547020B2
JP2547020B2 JP62134367A JP13436787A JP2547020B2 JP 2547020 B2 JP2547020 B2 JP 2547020B2 JP 62134367 A JP62134367 A JP 62134367A JP 13436787 A JP13436787 A JP 13436787A JP 2547020 B2 JP2547020 B2 JP 2547020B2
Authority
JP
Japan
Prior art keywords
alloy
amorphous
atomic
corrosion resistance
nickel alloy
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
Application number
JP62134367A
Other languages
Japanese (ja)
Other versions
JPS63297532A (en
Inventor
功二 橋本
章 三橋
勝彦 浅見
朝日 川嶋
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 Materials Corp
Original Assignee
Mitsubishi Materials Corp
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
Priority to JP62134367A priority Critical patent/JP2547020B2/en
Application filed by Mitsubishi Materials Corp filed Critical Mitsubishi Materials Corp
Priority to PCT/JP1988/000449 priority patent/WO1988008885A1/en
Priority to DE3853190T priority patent/DE3853190T2/en
Priority to EP88903960A priority patent/EP0314805B1/en
Priority to KR1019890700011A priority patent/KR940004900B1/en
Publication of JPS63297532A publication Critical patent/JPS63297532A/en
Priority to FI890031A priority patent/FI98074C/en
Priority to US07/914,027 priority patent/US5634989A/en
Application granted granted Critical
Publication of JP2547020B2 publication Critical patent/JP2547020B2/en
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

Links

Landscapes

  • Physical Vapour Deposition (AREA)
  • Continuous Casting (AREA)

Description

【発明の詳細な説明】 産業上の利用分野 本発明は、高温濃リン酸のような過酷な腐食性環境に
おける耐食材料として好適な高耐食アモルファスニッケ
ル合金に関するものである。
Description: FIELD OF THE INVENTION The present invention relates to a high corrosion resistant amorphous nickel alloy suitable as a corrosion resistant material in a severe corrosive environment such as high temperature concentrated phosphoric acid.

従来の技術 現在、高温濃厚リン酸プラント用構造材料として30
9、310、446Moステンレス鋼クロムモリブデンチタン
鋼、ハステロイCなどが使われているが、これらといえ
ども高温濃リン酸のような激しい耐食性環境下では十分
な耐食性を備えてはいない。
Conventional technology Currently, as a structural material for high temperature concentrated phosphoric acid plant, 30
9, 310, 446Mo stainless steel chrome molybdenum titanium steel, Hastelloy C, etc. are used, but none of them have sufficient corrosion resistance under the severe corrosion resistance environment such as high temperature concentrated phosphoric acid.

通常、合金は固体状態では結晶化しているが合金組成
を限定して溶融状態から超急冷凝固させるなど、個体形
成の過程で原子配列に長周期的規則性を形成させない方
法を適用すると、結晶構造を持たず、液体に類似したア
モルファス構造が得られ、このような合金をアモルファ
ス合金という。
Normally, alloys are crystallized in the solid state, but applying a method that does not form long-period regularity in the atomic arrangement in the process of solid formation, such as limiting the alloy composition and rapidly quenching and solidifying from the molten state, , And an amorphous structure similar to a liquid is obtained. Such an alloy is called an amorphous alloy.

アモルファス合金は多くは過飽和固溶体の均一な単相
合金であって、従来の実用合金に比べて著しく高い強度
を保有し、かつ組成に応じて異常に高い耐食性をはじめ
種々の特性を示す。本発明者らはこのようなアモルファ
ス合金の特性を活用する研究を行った結果、強酸あるい
は高濃度の塩素イオンを含む水溶液中においても孔食、
隙間腐食および全面腐食を受けない高耐食アモルファス
ニッケル合金を見いだし、先に説く願昭51−132290号と
して出願し、また、沸騰濃度硝酸あるいは更に酸化剤を
含むような過酷な腐食性環境で使用し得る高耐食アモル
ファス合金を見出し、特願昭60−51036号として特許出
願し、更に、沸騰濃硝酸のような過酷な腐食性環境で使
用し得る高耐食アモルファス合金を見出し、特願昭60−
172860号および特願昭60−172861号として特許出願し
た。これらは、いずれもアモルファスニッケル合金であ
る。前述のように濃厚リン酸は沸点が高いために、高温
で特に腐食性が激しく、合金自体が安定な保護皮膜を形
成する能力を持たないと腐食性は得られない。
Amorphous alloys are mostly homogeneous single-phase alloys of supersaturated solid solutions, have significantly higher strength than conventional practical alloys, and exhibit various properties, such as abnormally high corrosion resistance, depending on the composition. The present inventors have conducted research utilizing the properties of such an amorphous alloy, and found that pitting corrosion occurs even in an aqueous solution containing a strong acid or a high concentration of chloride ions.
We have found a highly corrosion-resistant amorphous nickel alloy that does not undergo crevice corrosion and general corrosion, and filed as Japanese Patent Application No. 51-132290, which was previously explained. Found a highly corrosion-resistant amorphous alloy and applied for a patent as Japanese Patent Application No. 60-51036.Furthermore, found a highly corrosion-resistant amorphous alloy that can be used in a severe corrosive environment such as boiling concentrated nitric acid.
Patent applications were filed as 172860 and Japanese Patent Application No. 60-172861. All of these are amorphous nickel alloys. Since concentrated phosphoric acid has a high boiling point as described above, it is particularly corrosive at high temperatures, and corrosiveness cannot be obtained unless the alloy itself has the ability to form a stable protective film.

本発明者らは、アモルファス合金の種々の特性を検討
しながら更に研究を行った結果、前記特願昭51−132290
号、60−51036号、引例1特開昭62−33735号および60−
172861号に記載の合金の中でも特に保護皮膜形成能力の
高い合金あるいは類似の合金に更に保護皮膜形成能力を
高める元素を添加することによって、高温濃厚リン酸の
ような酸化力に乏しく過酷な腐食性酸中でも安定な保護
皮膜を形成して高耐食性を備えたアモルファスニッケル
合金が得られることを見出し、先に特願昭61−225435号
および特願昭61−225436号を出願した。
As a result of further research while studying various characteristics of amorphous alloys, the inventors of the present invention have disclosed the above-mentioned Japanese Patent Application No. 51-132290.
No. 60-51036, Reference 1 JP-A-62-33735 and 60-
Among the alloys described in No. 172861, particularly by adding an element that further enhances the protective film forming ability to an alloy having a high protective film forming ability or a similar alloy, oxidative power such as high temperature concentrated phosphoric acid is poor and severe corrosiveness It was found that an amorphous nickel alloy having a high corrosion resistance can be obtained by forming a stable protective film even in an acid, and previously filed Japanese Patent Application Nos. 61-225435 and 61-225436.

発明が解決しようとする問題点 濃厚リン酸は沸点が高いために高温で特に腐食性が激
しく、通常の市販金属材料で安全に使用し得るものはな
い。このような環境においても前記特願昭61−225435お
よび特願昭61−225436に記載の合金は耐食性を示すが、
通常の金属材料の使用がきわめて困難なこのような腐食
性環境において、使用に耐える更に種々の新しい金属材
料の出現が求められている。
Problems to be Solved by the Invention Since concentrated phosphoric acid has a high boiling point, it is particularly corrosive at high temperatures, and no ordinary commercially available metallic material can be safely used. Even in such an environment, the alloys described in Japanese Patent Application No. 61-225435 and Japanese Patent Application No. 61-225436 exhibit corrosion resistance,
In such a corrosive environment where the use of ordinary metallic materials is extremely difficult, there is a demand for the development of various new metallic materials that can withstand use.

問題点を解決するための手段 本発明の目的は高温濃リン酸のように非酸化性で金属
を不動体化しにくく、かつきわめて過酷な腐食性を備え
た環境に耐える合金を提供することにある。
Means for Solving the Problems An object of the present invention is to provide an alloy which is non-oxidizing such as high temperature concentrated phosphoric acid, which hardly immobilizes metals, and has an environment with extremely severe corrosiveness. .

本発明者らは、アモルファス合金の耐食性に関する研
究を継続した結果、前記特願昭61−225435号ならびに特
願昭61−225436号に記載の合金以外にも、種々の元素の
組合わせによって、高温濃厚リン酸中において高耐食性
を示すアモルファスニッケル合金が得られることを見い
だし、本発明を達成した。
The present inventors, as a result of continuing research on the corrosion resistance of amorphous alloys, in addition to the alloys described in Japanese Patent Application No. 61-225435 and Japanese Patent Application No. 61-225436, by combining various elements, high temperature The present invention has been accomplished by finding that an amorphous nickel alloy having high corrosion resistance can be obtained in concentrated phosphoric acid.

本発明は、特許請求の範囲第1項ないし第4項に示す
第1ないし第4の発明からなるものであるが、次の第1
表にこれら第1ないし第4の発明の構成元素および含有
率を示す。
The present invention comprises the first to fourth inventions set forth in claims 1 to 4, and the following first
The constituent elements and contents of these first to fourth inventions are shown in the table.

作用 上記組成の溶融合金を超急冷凝固させたり、スパッタ
デポジションさせるなどアモルファス合金を作成する種
々の方法によって得られるアモルファス合金は前記各元
素が均一に固溶した単相合金である。そのため、本発明
のアモルファスニッケル合金には、きわめて均一で高耐
食性を保証する保護皮膜が生成する。
Action Amorphous alloys obtained by various methods for producing amorphous alloys, such as ultra-rapid solidification of a molten alloy having the above composition or sputter deposition, are single-phase alloys in which the above elements are uniformly solid-dissolved. Therefore, the amorphous nickel alloy of the present invention forms a protective film that is extremely uniform and guarantees high corrosion resistance.

酸化力の弱い高温濃厚リン酸溶液中で金属材料派、用
意に溶解するため、このような環境で金属材料を使用す
るためには、安全な保護皮膜を生成する能力を金属材料
に付与する必要がある。これは、有効元素を必要量含む
合金を作ることによって実現される。しかし、結晶質金
属の場合、多種多量の合金元素を添加すると、しばしば
化学的性質の異なる多相構造となり、所定の耐食性が実
現し得ないことがある。また、化学的不均一性の発生は
むしろ耐食性に有害である。
In order to use a metal material in such an environment, it is necessary to give the metal material the ability to form a safe protective film because it dissolves easily in a high temperature concentrated phosphoric acid solution with weak oxidizing power. There is. This is achieved by making an alloy containing the required amount of active elements. However, in the case of a crystalline metal, if a large amount of various alloying elements are added, a polyphase structure having different chemical properties is often obtained, and a predetermined corrosion resistance may not be realized. Also, the occurrence of chemical heterogeneity is rather detrimental to corrosion resistance.

これに対し、本発明のアモルフィス合金は均一固溶体
であり、安全な保護皮膜を形成させ得る所定量の有効元
素を均一に含むためのものである。このようなアモルフ
ァスニッケル合金には、均一な保護皮膜が生じ、十分に
高い耐食性を発揮する。
On the other hand, the amorphis alloy of the present invention is a uniform solid solution and is intended to uniformly contain a predetermined amount of effective element capable of forming a safe protective film. Such an amorphous nickel alloy has a uniform protective film, and exhibits sufficiently high corrosion resistance.

すなわち、酸化力の弱い高温の濃リン酸に耐える金属
材料が備えるべき条件は、非酸化性環境で安定な保護皮
膜が材料に均一に生じる高い保護皮膜形成能力を持つこ
とである。これは本発明の合金組成で実現され、また合
金がアモルファス構造を有することは、複雑な組成の合
金を単相固溶体として作成することを可能にし、均一な
保護皮膜形成を保証するものである。
That is, the condition that a metal material having a weak oxidizing power and that can withstand concentrated phosphoric acid at high temperature is to have a high protective film-forming ability that a stable protective film is uniformly formed on the material in a non-oxidizing environment. This is realized by the alloy composition of the present invention, and the fact that the alloy has an amorphous structure allows an alloy having a complicated composition to be prepared as a single-phase solid solution, and ensures uniform formation of a protective film.

次に、本発明における各成分組成を限定する理由を述
べる。
Next, the reasons for limiting the composition of each component in the present invention will be described.

Niは本発明合金の基礎となる元素であって、Moおよび
CrとTaとの合計が所定の量共存する場合にはアモルファ
ス構造を形成する元素であり、またPと共存してもアモ
ルファス構造を形成する元素である。更に、Niは耐食性
を担うTa、Mo、Crの作用を助ける元素である。
Ni is a basic element of the alloy of the present invention, and Mo and
It is an element that forms an amorphous structure when the total amount of Cr and Ta coexists in a predetermined amount, and an element that forms an amorphous structure even when it coexists with P. Further, Ni is an element that assists the actions of Ta, Mo, and Cr, which are responsible for corrosion resistance.

Ta、Mo、Crは何れも保護皮膜を形成して耐食性を担う
元素である。これらのうちTaと他の元素との総和が25−
50原子%であるとき、これらとNiとの金属−金属合金は
アモルファス構造を形成し得るため、本発明の第1項か
ら第6項においてMoおよびCrとTaとの合計は25−50原子
%とする。PはTa、Mo、Crなどの保護皮膜の形成を助け
る有効な元素であるが、金属−金属合金に多量に添加す
るとアモルファス構造が得がたくなるため、本発明の第
3項および第4項においてPは10原子%未満とする。
Ta, Mo, and Cr are elements that form a protective film and play a role in corrosion resistance. Of these, the sum of Ta and other elements is 25-
When the content is 50 atomic%, since the metal-metal alloy of these and Ni can form an amorphous structure, the sum of Mo and Cr and Ta in the first to sixth aspects of the present invention is 25-50 atomic%. And P is an effective element that assists the formation of a protective film such as Ta, Mo, Cr, etc., but if added in a large amount to a metal-metal alloy, it becomes difficult to obtain an amorphous structure, and therefore, the third and fourth aspects of the present invention. In, P is less than 10 atomic%.

また、本発明のアモルファスニッケル合金が10原子%
以下のNb、5原子%以下のTi、Zrを含んでも本発明の目
的に支障はない。
Further, the amorphous nickel alloy of the present invention contains 10 atomic%
Even if the following Nb and 5 atomic% or less of Ti and Zr are included, the object of the present invention is not hindered.

本発明のアモルファス合金の作製には、既に広く用い
られている種々の方法、即ち、液体合金を超急冷凝固さ
せる方法、気相を経てアモルファス合金を形成させる種
々の方法、イオン注入によって固体の長周期構造を破壊
する方法などアモルファス合金を作製するいずれの方法
でもよい。
In the production of the amorphous alloy of the present invention, various methods which are already widely used, that is, a method of rapidly quenching and solidifying a liquid alloy, various methods of forming an amorphous alloy through a gas phase, and a method of forming a solid long by ion implantation are used. Any method of producing an amorphous alloy such as a method of destroying the periodic structure may be used.

一例として本発明のアモルファス合金を作製する装置
を第1図に示す。点線で囲んだ部分は真空にした後、不
活性ガスで満たされる。図において2は下方先端に垂直
ノズル3を有する石英管で、この石英管2の上端に設け
られている送入口1より原料4ならびに原料の酸化を防
止する不活性ガスを送入することができる。前記試料を
加熱するため石英管2の周囲に加熱炉5を設置する。ノ
ズル3の垂直下方に高速回転ロール7を置き、これをモ
ーター6によって回転させる。アモルファス合金の作製
には、所定の組成の原料4を石英管2内に入れ、まず、
装置を10-5Torr程度の真空にした後、不活性ガスを満た
す。次いで、原料4を加熱炉5によって加熱溶融し、こ
の溶融金属をモーター6によって1000−10000r.p.mで高
速回転しているロール7の外周面上に加圧不活性ガスを
用いて噴射させることによって行われる。この方法によ
って、例えば厚さ0.1mm、幅10mm、長さ数m程度の長い
薄板として、本発明のアモルファス合金を得ることがで
きる。
As an example, FIG. 1 shows an apparatus for producing the amorphous alloy of the present invention. The part surrounded by the dotted line is filled with an inert gas after being evacuated. In the figure, reference numeral 2 denotes a quartz tube having a vertical nozzle 3 at a lower end thereof. A raw material 4 and an inert gas for preventing the raw material from being oxidized can be fed from a feed port 1 provided at the upper end of the quartz tube 2. . A heating furnace 5 is provided around the quartz tube 2 to heat the sample. A high-speed rotating roll 7 is placed vertically below the nozzle 3 and rotated by a motor 6. To prepare an amorphous alloy, a raw material 4 having a predetermined composition is placed in a quartz tube 2 and first,
The apparatus is evacuated to about 10 -5 Torr and then filled with an inert gas. Then, the raw material 4 is heated and melted by the heating furnace 5, and the molten metal is sprayed by the motor 6 onto the outer peripheral surface of the roll 7 which is rotating at a high speed of 1000-10000 r.pm by using a pressurized inert gas. Done. By this method, the amorphous alloy of the present invention can be obtained as a long thin plate having a thickness of about 0.1 mm, a width of 10 mm, and a length of about several meters.

実施例 第2表に示す組成となるように原料金属を混合し、ア
ルゴンアーク溶融炉により原料合金を作製した。これら
の合金をアルゴン雰囲気中で再溶融し、図1に示した単
ロール法を用いて超急冷凝固させることにより、厚さ0.
01−0.05mm,幅1−3mm、長さ3−20mのアモルファス合
金薄板を得た。アモルファス構造形成の確認はX線回折
によって行った。これらの合金試料の表面をシリコンカ
ーバイド紙1000番までシクロヘキサン中で研摩した。次
いで所定の長さの合金原料を切り出し、160℃の約63%P
2O5および200℃の72%P2O5溶液に7−10日間浸漬し、浸
漬前後の重量をマイクロバランスを用いて測定した。
Example Raw material metals were mixed so as to have the composition shown in Table 2, and a raw material alloy was produced by an argon arc melting furnace. These alloys were re-melted in an argon atmosphere and were rapidly quenched and solidified using the single roll method shown in FIG.
An amorphous alloy thin plate having a length of 01-0.05 mm, a width of 1-3 mm and a length of 3-20 m was obtained. The formation of the amorphous structure was confirmed by X-ray diffraction. The surfaces of these alloy samples were polished in cyclohexane up to silicon carbide paper No. 1000. Then, cut out the alloy raw material of the specified length, and about 63% P at 160 ℃
It was dipped in a 72% P 2 O 5 solution of 2 O 5 and 200 ° C. for 7 to 10 days, and the weight before and after the immersion was measured using a microbalance.

得られた結果を第3表に示す。 The results obtained are shown in Table 3.

本発明のアモルファス合金の腐食速度はきわめて小さ
い。また、本発明の合金を浸漬試験の後、合金表面をX
線光電子分光法を用いて解析した結果、合金はTaおよび
Moが濃縮した水和オキシ水酸化物保護皮膜が生じてお
り、これが本発明合金の高耐食性の原因であることが判
明した。
The corrosion rate of the amorphous alloy of the present invention is extremely low. After the immersion test of the alloy of the present invention,
As a result of analysis using X-ray photoelectron spectroscopy, the alloy was Ta and
A hydrated oxyhydroxide protective film in which Mo was concentrated was formed, and it was found that this is the cause of the high corrosion resistance of the alloy of the present invention.

発明の効果 以上詳述したとうり、本発明のアモルファスニッケル
合金は、酸化物の乏しい高温リン酸のような激しい腐食
性環境においても安定な保護皮膜を形成して、腐食され
ない高耐食合金である。
Effect of the Invention As described in detail above, the amorphous nickel alloy of the present invention is a highly corrosion-resistant alloy that forms a stable protective film even in a severe corrosive environment such as high-temperature phosphoric acid with poor oxide and is not corroded. .

また、本発明の合金の作製には、既に広く用いられて
いるアモルファス合金作製の技術のいずれをも適用でき
るため、特殊な装置を改めて必要とせず、本発明合金は
実用性にも優れている。
In addition, since the alloy of the present invention can be applied to any of the widely used techniques for producing an amorphous alloy, a special device is not required again, and the alloy of the present invention is excellent in practicality. .

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

第1図は本発明アモルファス合金を作製する装置の一例
を示す概略図である。 1:原料送入口 2:石英管 3:ノズル部 4:原料 5:加熱炉 6:モーター 7:高速回転ロール
FIG. 1 is a schematic view showing an example of an apparatus for producing the amorphous alloy of the present invention. 1: Raw material inlet 2: Quartz tube 3: Nozzle part 4: Raw material 5: Heating furnace 6: Motor 7: High-speed rotating roll

Claims (4)

(57)【特許請求の範囲】(57) [Claims] 【請求項1】Taを10−40原子%とMoとTaの合計量で25−
50原子%含み残部は実質的にNiからなる高耐食アモルフ
ァスニッケル合金。
1. A Ta content of 10-40 atomic% and a total content of Mo and Ta of 25-
Highly corrosion resistant amorphous nickel alloy with 50 atomic% and balance Ni.
【請求項2】Taを10−40原子%とMo、Cr、Taの3元素の
合計量で25−50原子%含み残部は実質的にNiからなる高
耐食アモルファスニッケル合金。
2. A highly corrosion-resistant amorphous nickel alloy containing 10-40 atomic% of Ta and 25-50 atomic% of the total amount of three elements of Mo, Cr and Ta, and the balance being substantially Ni.
【請求項3】Taを10−40原子%とMoをTaとの合計量で25
−50原子%含み更にPを10原子%未満含み残部はNiから
なる高耐食アモルファスニッケル合金。
3. The total amount of Ta is 10-40 atomic% and Mo is 25.
A highly corrosion-resistant amorphous nickel alloy containing -50 atomic% and less than 10 atomic% P and the balance Ni.
【請求項4】Taを10−40原子%とMo、Cr、Taの3元素の
合計量で25−50原子%含み更にPを10原子%未満含み残
部は実質的にNiからなる高耐食アモルファスニッケル合
金。
4. A highly corrosion-resistant amorphous material containing 10-40 atomic% of Ta, 25-50 atomic% of the total amount of three elements of Mo, Cr and Ta, further containing less than 10 atomic% of P and the balance of Ni. Nickel alloy.
JP62134367A 1987-05-07 1987-05-29 High corrosion resistance amorphous nickel alloy Expired - Fee Related JP2547020B2 (en)

Priority Applications (7)

Application Number Priority Date Filing Date Title
JP62134367A JP2547020B2 (en) 1987-05-29 1987-05-29 High corrosion resistance amorphous nickel alloy
DE3853190T DE3853190T2 (en) 1987-05-07 1988-05-07 HIGH CORROSION-RESISTANT AMORPHOUS ALLOY.
EP88903960A EP0314805B1 (en) 1987-05-07 1988-05-07 Highly corrosion-resistant amorphous nickel-based alloy
KR1019890700011A KR940004900B1 (en) 1987-05-07 1988-05-07 Highly corrosion-resistant amorphous alloy
PCT/JP1988/000449 WO1988008885A1 (en) 1987-05-07 1988-05-07 Highly corrosion-resistant amorphous alloy
FI890031A FI98074C (en) 1987-05-07 1989-01-04 Amorphous nickel alloy for use in corrosive environments
US07/914,027 US5634989A (en) 1987-05-07 1992-07-15 Amorphous nickel alloy having high corrosion resistance

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP62134367A JP2547020B2 (en) 1987-05-29 1987-05-29 High corrosion resistance amorphous nickel alloy

Related Child Applications (1)

Application Number Title Priority Date Filing Date
JP33385895A Division JPH08225901A (en) 1995-11-17 1995-11-17 Amorphous nickel alloy high in corrosion resistance

Publications (2)

Publication Number Publication Date
JPS63297532A JPS63297532A (en) 1988-12-05
JP2547020B2 true JP2547020B2 (en) 1996-10-23

Family

ID=15126719

Family Applications (1)

Application Number Title Priority Date Filing Date
JP62134367A Expired - Fee Related JP2547020B2 (en) 1987-05-07 1987-05-29 High corrosion resistance amorphous nickel alloy

Country Status (1)

Country Link
JP (1) JP2547020B2 (en)

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2569331B2 (en) * 1987-05-29 1997-01-08 三菱マテリアル株式会社 High corrosion resistant amorphous nickel alloy for high temperature concentrated sulfuric acid
WO2024046742A1 (en) 2022-08-29 2024-03-07 Universität des Saarlandes Alloy for producing bulk metallic glasses and shaped bodies therefrom

Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS6233735A (en) * 1985-08-06 1987-02-13 Mitsui Eng & Shipbuild Co Ltd Amorphous alloy having high corrosion resistance
JPS63297533A (en) * 1987-05-29 1988-12-05 Mitsubishi Metal Corp High corrosion resistant amorphous nickel alloy for high temperature concentrated sulfuric acid

Patent Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS6233735A (en) * 1985-08-06 1987-02-13 Mitsui Eng & Shipbuild Co Ltd Amorphous alloy having high corrosion resistance
JPS63297533A (en) * 1987-05-29 1988-12-05 Mitsubishi Metal Corp High corrosion resistant amorphous nickel alloy for high temperature concentrated sulfuric acid

Also Published As

Publication number Publication date
JPS63297532A (en) 1988-12-05

Similar Documents

Publication Publication Date Title
US5634989A (en) Amorphous nickel alloy having high corrosion resistance
JPH0676631B2 (en) High corrosion resistance Amorph Asnickel alloy
US4968363A (en) Method of preventing corrosion of a material against hydrochloric acid
Pang et al. Effects of chromium on the glass formation and corrosion behavior of bulk glassy Fe-Cr-Mo-CB alloys
JPS6379931A (en) Highly corrosion-resistant amorphous nickel alloy
Hashimoto What we have learned from studies on chemical properties of amorphous alloys?
Hashimoto et al. Recent progress in corrosion-resistant metastable alloys
Sharma et al. Influence of nitrogen ion implantation on corrosion behavior of Zr55Cu30Ni5Al10 amorphous alloy
JPS63270435A (en) High corrosion resistant amorphous alloy
JPH0615706B2 (en) High corrosion resistant amorphous alloy
JP2937580B2 (en) High corrosion resistant amorphous alloy
Pang et al. Formation of bulk glassy Ni-(Co-) Nb-Ti-Zr alloys with high corrosion resistance
JP2547020B2 (en) High corrosion resistance amorphous nickel alloy
JP2569331B2 (en) High corrosion resistant amorphous nickel alloy for high temperature concentrated sulfuric acid
EP0314805B1 (en) Highly corrosion-resistant amorphous nickel-based alloy
EP0055403B1 (en) Amorphous alloys of nickel, aluminum and boron
JPH0535212B2 (en)
JPH08225901A (en) Amorphous nickel alloy high in corrosion resistance
JPH0465897B2 (en)
JPH07103454B2 (en) High corrosion resistance amorphous alloy
Hashimoto et al. Extremely corrosion-resistant bulk amorphous alloys
JPH0465895B2 (en)
Garg et al. Zr--Re phase diagram between 1866 to 1913/sup 0/K
JPS6379932A (en) Highly corrosion-resistant amorphous alloy
JPH0119457B2 (en)

Legal Events

Date Code Title Description
R250 Receipt of annual fees

Free format text: JAPANESE INTERMEDIATE CODE: R250

LAPS Cancellation because of no payment of annual fees