EP2610371B1 - Verfahren zum Herstellen von Rhenium-Nickellegierungen - Google Patents

Verfahren zum Herstellen von Rhenium-Nickellegierungen Download PDF

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Publication number
EP2610371B1
EP2610371B1 EP12460097.4A EP12460097A EP2610371B1 EP 2610371 B1 EP2610371 B1 EP 2610371B1 EP 12460097 A EP12460097 A EP 12460097A EP 2610371 B1 EP2610371 B1 EP 2610371B1
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EP
European Patent Office
Prior art keywords
rhenium
nickel
cathode
electrodeposition
vii
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.)
Active
Application number
EP12460097.4A
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English (en)
French (fr)
Other versions
EP2610371A1 (de
Inventor
Dorota Kopyto
Mieczyslaw Kwarcinski
Andrzej Chmielarz
Grzegorz Benke
Krystyna Anyszkiewicz
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.)
Instytut Metali Niezelaznych
Instytut Nawozow Sztucznych
Original Assignee
Instytut Metali Niezelaznych
Instytut Nawozow Sztucznych
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Application filed by Instytut Metali Niezelaznych, Instytut Nawozow Sztucznych filed Critical Instytut Metali Niezelaznych
Priority to PL12460097T priority Critical patent/PL2610371T3/pl
Publication of EP2610371A1 publication Critical patent/EP2610371A1/de
Application granted granted Critical
Publication of EP2610371B1 publication Critical patent/EP2610371B1/de
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Classifications

    • C—CHEMISTRY; METALLURGY
    • C25—ELECTROLYTIC OR ELECTROPHORETIC PROCESSES; APPARATUS THEREFOR
    • C25D—PROCESSES FOR THE ELECTROLYTIC OR ELECTROPHORETIC PRODUCTION OF COATINGS; ELECTROFORMING; APPARATUS THEREFOR
    • C25D3/00—Electroplating: Baths therefor
    • C25D3/02—Electroplating: Baths therefor from solutions
    • C25D3/56—Electroplating: Baths therefor from solutions of alloys
    • C—CHEMISTRY; METALLURGY
    • C25—ELECTROLYTIC OR ELECTROPHORETIC PROCESSES; APPARATUS THEREFOR
    • C25D—PROCESSES FOR THE ELECTROLYTIC OR ELECTROPHORETIC PRODUCTION OF COATINGS; ELECTROFORMING; APPARATUS THEREFOR
    • C25D3/00—Electroplating: Baths therefor
    • C25D3/02—Electroplating: Baths therefor from solutions
    • C25D3/56—Electroplating: Baths therefor from solutions of alloys
    • C25D3/562—Electroplating: Baths therefor from solutions of alloys containing more than 50% by weight of iron or nickel or cobalt

Definitions

  • the subject of this invention is a method for producing homogeneous rhenium - nickel alloys by electrodeposition from aqueous solutions.
  • Rhenium being a high-melting metal, with a number of unique properties, is gaining on significance as a high quality engineering material. Properties of rhenium promote its application in many areas of technology, such as aviation, space engineering, nuclear engineering, electrical engineering, biomedicine.
  • the application of rhenium as a component of superalloys used, for instance, in the manufacture of jet engine turbine blades, is quickly expanding. Addition of 3 to 6% Re to nickel superalloys enables engine operation at higher temperatures, at higher speed, improving thereby both engine performance and fuel economy.
  • the two currently applied methods of producing metallic rhenium include powder metallurgy (PM) and chemical vapour deposition (CVD). These processes are expensive, complex and energy-consuming. Electrodeposition of rhenium and its alloys, carried out at low temperatures and in nontoxic aqueous solutions, requiring low energy input, may be an alternative to methods applied hitherto.
  • the dense, metallic and uniform cathodic deposits constitute an excellent material for preliminary alloys for creating rhenium-containing special alloys or superalloys.
  • a method of forming high temperature resistant rhenium alloy coating films described in patent specification US 7368048 consists in the use of an electrolyte that contains ions of rhenate(VII), alloy metal selected from the group consisting of Ni, Co, Fe and Cr(III), Li and Na, and an organic acid selected from the group consisting of carboxylic acids or aminocarboxylic acids (e.g. citric acid), acting as a complexing agent.
  • This method enables obtaining 10 to 30 ⁇ m thick plated films of appropriate quality at a current density of 10 A/dm 2 .
  • Patent specification US 3668083 presents a method of electrodeposition of rhenium and its alloys in the form of low-stressed coating films from rhenium bath containing additionally one or more chemical compounds selected from the group consisting of the following salts: magnesium sulphate, magnesium sulphamate, aluminium sulphate and aluminium sulphamate.
  • the agents that provided formation of good quality coating films were additives to the electrolyte in the form of conducting salts, complexing compounds, salts that stabilized processes in the near-electrode zones, or sulphamate ions rendering formation of fine-crystalline deposits of high plasticity and low stress.
  • These processes relate to the forming of thin coatings, rather than to bulk production of solid rhenium alloys.
  • the method of preparing electrolytic rhenium - nickel alloys according to this invention consists in the use of a sulphate nickel electrolyte, comprising nickel(II) sulphate, sodium sulphate and boric acid, supplemented by ammonium rhenate(VII) added in an amount of 2 to 100 g/dm 3 .
  • the cathodic process of depositing the rhenium-nickel alloy proceeds on a centrally arranged cathode. Insoluble anodes are placed on both sides of the cathode. The process is conducted under conditions of stabilizing pH in the near-cathode zone.
  • the method of preparing rhenium-nickel alloys according to the invention consists in electrodepositing them at temperatures of from 10 to 80°C and at current density ⁇ 5 A/dm 2 and pH of the electrolytic bath of from 1 to 8. Under these conditions the obtained rhenium - nickel alloy deposit has a dense, metallic, smooth, uniform structure, and it is produced at a high current efficiency of ⁇ 95% and low specific power consumption of within 2.0 to 2.5 kWh per kg of alloy.
  • the cathodic alloy deposits obtained after 48 hours of the electrodeposition process have a thickness > 1.5 mm and the following content of the main components:
  • the advantage of the invention presented is that a dense and uniform deposit of rhenium-nickel alloy is obtained in the form of a solid solution containing up to 80 wt% rhenium.
  • the latter can be used for the production of special alloys.
  • the method according to the invention is illustrated in the examples below.
  • An electrolytic tank is filled with nickel - rhenium electrolytic bath containing 11.5 g/dm 3 rhenium in the form of ammonium rhenate(VII), 40.0 g/dm 3 nickel in the form of nickel(II) sulphate, 10.0 g/dm 3 boric acid and 80.0 g/dm 3 sodium sulphate.
  • the process of rhenium - nickel alloy electrodeposition is conducted without electrolyte flow, making up for evaporation losses and for rhenium and nickel ions consumption caused by deposition of the alloy on the cathode, at the temperature of 55°C, at cathodic current density of 1.2 A/dm 2 and pH of the electrolytic bath of from 1.8 to 4.1.
  • the rhenium - nickel alloy deposit obtained on a copper cathode had a thickness of ca. 1.5 mm; it was dense, metallic, lustrous; it adhered tightly to the core, contained 47.9 wt% rhenium (22.5 atomic %) and 51.9 wt% nickel (77.5 atomic %).
  • the current efficiency of depositing the alloy of the above composition was 99.0%, with specific power consumption amounting to 2.15 kWh per kg of alloy.
  • the process of rhenium - nickel alloy electrodeposition was conducted in a flow electrolyzer, wherein the electrolyte was fed to the bottom of the electrolyzer and was carried away through a weir in the top part of the electrolyzer.
  • the flow of electrolyte was laminar, parallel to the surfaces of the cathode and of the anodes, stabilizing thereby pH in the cathode area and carrying excess hydrogen ions away from the electrolyzer.
  • the nickel - rhenium electrolyte used contained 13.6 g/dm 3 rhenium in the form of ammonium rhenate(VII), 47.8 g/dm 3 nickel in the form of nickel(II) sulphate, 10.0 g/dm 3 boric acid and 80.0 g/dm 3 sodium sulphate.
  • the process was conducted at the temperature of 55°C, at cathodic current density of 1.5 A/dm 2 and pH of the electrolyte of from 2.4 to 3.6.
  • Linear flow velocity of the electrolyte was 3.0 cm/min, and the volumetric charge density was 3.0 Ah/dm 3 .
  • cathodic rhenium - nickel alloy deposit was lustrous, metallic, fine-crystalline, with no cracks or dendrites; its thickness was ca. 1.5 mm; it contained 46.1 wt% rhenium (21.4 atomic %) and 53.5 wt% nickel (78.6 atomic %).
  • the current efficiency of depositing this alloy was 99.9%, with specific power consumption amounting to 2.13 kWh per kg of alloy.

Landscapes

  • Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Electrochemistry (AREA)
  • Materials Engineering (AREA)
  • Metallurgy (AREA)
  • Organic Chemistry (AREA)
  • Electroplating And Plating Baths Therefor (AREA)
  • Electrolytic Production Of Metals (AREA)

Claims (1)

  1. Die Gewinnungsart homogener Rhenium-Nickel-Legierungen durch Elektroabscheidung aus Wasserlösungen, die sich dadurch charakterisiert, dass in ein Nickelsulfat-Elektrolytenbad, das zur Herstellung von Nickelkathoden verwendet wird, 2 bis 100 g/dm3 Rhenium in Form von Rhenat(VII)-Ionen am besten als Ammonium(VII)-Rhenat eingeführt werden und bei einer Temperatur von 10 bis 80°C, am besten bei ca. 55°C an einer im Elektrolyseur zentral angebrachten Kathode an deren beiden Seiten unlösliche Anoden, um besten Titananoden mit Metalloxiden beschichtet, anzubrigen sind die
    Elektroabscheidung einer Rhenium-Nickel-Legierung erfolgt. Dabei sind die Kathodenstromdichte von ≤ 5 A/dm2 und der pH-Wert des Elektrolyten 1 bis 8 anzupassen. Der laminare Elektrolyten-Durchfluss hat mit einer Lincargeschwindigkeit von 1 bis 5 cm/min für die elektrische Ladangschichte von 1 bis 5 Ah/dm3 zu erfolgen.
EP12460097.4A 2011-12-27 2012-12-27 Verfahren zum Herstellen von Rhenium-Nickellegierungen Active EP2610371B1 (de)

Priority Applications (1)

Application Number Priority Date Filing Date Title
PL12460097T PL2610371T3 (pl) 2011-12-27 2012-12-27 Sposób otrzymywania stopów ren - nikiel

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
PL397508A PL216443B1 (pl) 2011-12-27 2011-12-27 Sposób otrzymywania homogenicznych stopów ren-nikiel

Publications (2)

Publication Number Publication Date
EP2610371A1 EP2610371A1 (de) 2013-07-03
EP2610371B1 true EP2610371B1 (de) 2014-05-14

Family

ID=47603183

Family Applications (1)

Application Number Title Priority Date Filing Date
EP12460097.4A Active EP2610371B1 (de) 2011-12-27 2012-12-27 Verfahren zum Herstellen von Rhenium-Nickellegierungen

Country Status (3)

Country Link
EP (1) EP2610371B1 (de)
ES (1) ES2477328T3 (de)
PL (2) PL216443B1 (de)

Family Cites Families (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE1771763A1 (de) 1967-07-03
FR2770277A1 (fr) * 1997-10-29 1999-04-30 Framatome Sa Procede de reparation par chemisage d'un tube et utilisation du procede
WO2003062501A1 (fr) 2002-01-18 2003-07-31 Japan Science And Technology Agency Procede pour former un film de revetement en alliage de re ayant une teneur elevee en re par electroplacage

Also Published As

Publication number Publication date
EP2610371A1 (de) 2013-07-03
PL2610371T3 (pl) 2014-08-29
PL397508A1 (pl) 2013-03-18
PL216443B1 (pl) 2014-04-30
ES2477328T3 (es) 2014-07-16

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