EP4298270A1 - Procédé d'électrodéposition galvanique et bain galvanique associé - Google Patents

Procédé d'électrodéposition galvanique et bain galvanique associé

Info

Publication number
EP4298270A1
EP4298270A1 EP21716861.6A EP21716861A EP4298270A1 EP 4298270 A1 EP4298270 A1 EP 4298270A1 EP 21716861 A EP21716861 A EP 21716861A EP 4298270 A1 EP4298270 A1 EP 4298270A1
Authority
EP
European Patent Office
Prior art keywords
comprised
solution
per liter
grams per
aqueous solution
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
EP21716861.6A
Other languages
German (de)
English (en)
Inventor
Luca CAPACCIOLI
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.)
Italfimet SRL
Original Assignee
Italfimet SRL
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 Italfimet SRL filed Critical Italfimet SRL
Publication of EP4298270A1 publication Critical patent/EP4298270A1/fr
Pending legal-status Critical Current

Links

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
    • C25D3/62—Electroplating: Baths therefor from solutions of alloys containing more than 50% by weight of gold
    • C—CHEMISTRY; METALLURGY
    • C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
    • C22C—ALLOYS
    • C22C5/00—Alloys based on noble metals
    • C22C5/02—Alloys based on gold
    • C—CHEMISTRY; METALLURGY
    • C25—ELECTROLYTIC OR ELECTROPHORETIC PROCESSES; APPARATUS THEREFOR
    • C25D—PROCESSES FOR THE ELECTROLYTIC OR ELECTROPHORETIC PRODUCTION OF COATINGS; ELECTROFORMING; APPARATUS THEREFOR
    • C25D1/00—Electroforming
    • C25D1/02—Tubes; Rings; Hollow bodies
    • 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
    • C25D3/58—Electroplating: Baths therefor from solutions of alloys containing more than 50% by weight of copper
    • C—CHEMISTRY; METALLURGY
    • C25—ELECTROLYTIC OR ELECTROPHORETIC PROCESSES; APPARATUS THEREFOR
    • C25D—PROCESSES FOR THE ELECTROLYTIC OR ELECTROPHORETIC PRODUCTION OF COATINGS; ELECTROFORMING; APPARATUS THEREFOR
    • C25D7/00—Electroplating characterised by the article coated
    • C25D7/005—Jewels; Clockworks; Coins

Definitions

  • the present invention relates to a process for galvanic electrodeposition and to the associated galvanic bath, and also to a yellow gold alloy and to a use thereof.
  • the process provides an electrolytic reaction in a tank (galvanic bath), in which the object to be coated (which acts as a cathode) is immersed in an aqueous solution of the metal to be deposited.
  • the anode can be constituted by the metal itself to be deposited or also by an inert metal or by graphite.
  • a potential difference to the two electrodes by applying a potential difference to the two electrodes, a flow of ions of the metal to be deposited is generated and the metal progressively accumulates on the cathode, forming indeed the desired layer.
  • Yellow gold alloys are also known which comprise gold, copper and silver (and therefore lack cadmium); however, these alloys are soft and therefore unsuitable for uses in the field of electroforming. Moreover, it is substantially impossible to obtain a production with a constant gold fineness and therefore they are not used in commerce.
  • the aim of the present invention is to solve the problems described above, by providing a process for galvanic electrodeposition and/or a galvanic bath that allow to provide layers made of a 1N-3N yellow gold alloy, which have good solderability and high mechanical strength.
  • an object of the invention is to provide a process for galvanic electrodeposition and/or a galvanic bath that allow to obtain by electroforming shells or self-supporting objects made of a 1N-3N yellow gold alloy, with adequate metallic properties.
  • Another object of the invention is to provide a 1N-3N yellow gold alloy that can be used to provide shells or self-supporting objects obtained by electroforming.
  • Another object of the invention is to provide a process for galvanic electrodeposition and/or a galvanic bath that allow to obtain by electroforming shells or self-supporting objects made of a 1N-3N yellow gold alloy without resorting to silver and without using cadmium or other toxic substances.
  • Another object of the invention is to provide a process for galvanic electrodeposition and/or a galvanic bath that ensure high reliability in operation.
  • Another object of the invention is to provide an alloy and propose a process for preparing said alloy that can be obtained and executed easily starting from commonly commercially available elements and materials.
  • Another object of the invention is to provide an alloy and a process for preparing said alloy that have low costs and are safe in application.
  • the galvanic electrodeposition process comprises a step in which at least one object immersed in a galvanic bath which in turn comprises an aqueous solution is coated with a layer of yellow gold alloy.
  • the process is performed by applying a potential difference to two electrodes immersed in the bath: one electrode, the cathode, is constituted by the object to be coated, while the other one, the anode, can be constituted by the metal to be deposited, by an inert metal, by graphite, or others.
  • the flow of ions of the metal generated by the application of the potential difference causes the accumulation of said ions on the object, so as to obtain progressively the forming of the desired coating layer.
  • the possibility is provided to immerse a number of objects at will (of any shape and size), insofar as allowed by the dimensions of the tank filled with the aqueous solution and by the limitations and the technical requirements of each specific situation.
  • the process according to the invention can be used to deposit a protective layer intended to constitute an external layer or an underlayer (substrate) of the finished product that one wishes to obtain.
  • a protective layer intended to constitute an external layer or an underlayer (substrate) of the finished product that one wishes to obtain.
  • the process according to the invention is intended to be performed in the field of the technique also known as electroforming, according to which the object (core) that is coated during the process is subsequently removed, leaving a sort of self-supporting shell (electroformed product) which is indeed the actual goal of the process.
  • process according to the invention is intended to be have a preferred application in the field of fashion, leatherwear or jewelry, although other uses, which are in any case within the protective scope claimed herein, to provide finished products (or intermediate products) intended for other product markets are not excluded.
  • the aqueous solution comprises at least gold in a quantity comprised between 1 gram and 10 gram per liter of solution, in the form of alkaline cyanide.
  • the gold is preferably in the form of a potassium dicyanoaurate complex, but other practical choices (tetrachloroaurate, potassium tetracyanoaurate, or others still) are not excluded.
  • the aqueous solution comprises at least copper in a quantity comprised between 30 grams and 70 gram per liter of solution, in the form of an alkaline cyanide compound (and preferably in the form of cuprous cyanide).
  • the copper is preferably in the form of cuprous cyanide, but other practical choices (cuprous chloride, copper iodide, copper carbonate) are not excluded.
  • the aqueous solution comprises indium in a quantity comprised between 100 milligrams and 2 gram per liter of solution, in the form of a soluble compound (and preferably in the form of a soluble complex).
  • the aqueous solution comprises at least zinc in a quantity comprised between 100 milligrams and 2 grams per liter of solution, in the form of a soluble compound (and preferably in the form of a zinc complex).
  • the bath (and therefore the aqueous solution) is kept at a constant temperature comprised between 50°C and 80°C.
  • the solution is kept at a pH between 8 and 12.
  • the current density that is applied is comprised between 0,2 A/dm 2 e 1,5 A/dm 2 .
  • the bath (the aqueous solution) can be enriched with various other additives, some of which are mentioned by way of non-limiting example. With reference to these additives, it is specified that the solution can provide just one or several types among the ones that will be identified hereinafter, and that within the same type one or more different substances among the ones listed (or others still) might be present.
  • the aqueous solution can comprise free cyanide in a quantity comprised between 10 grams and 50 grams per liter of solution.
  • the aqueous solution can furthermore comprise a complexing agent, preferably in a quantity comprised between 5 grams and 30 grams per liter of solution.
  • a complexing agent is chosen from the group constituted by a carboxylic acid, an amino acid, a polyamine, an amine, and a phosphonic acid.
  • the aqueous solution can furthermore comprise a conducting salt, preferably in a quantity comprised between 10 grams and 100 grams per liter of solution.
  • the conducting salt is chosen in the group constituted by a citrate, a tartrate, an oxalate, a gluconate, a carbonate, a phosphate, and a sulfate.
  • the aqueous solution may furthermore comprise a wetting agent, preferably in a quantity comprised between 0.05 grams and 10 grams per liter of solution.
  • the wetting agent is chosen preferably in the group constituted by lauryl sulfate and a quaternary ammonium salt.
  • the aqueous solution can furthermore comprise also a grain refiner and/or a brightener.
  • the grain refiner and/or the brightener are preferably chosen from the group constituted by zirconium, iridium, selenium, antimony, tin, gallium, tellurium, germanium, bismuth, titanium, and silver.
  • the aqueous solution may furthermore comprise additional metals or elements in traces, which derive from the technical products used for its provision and preferably comprised in the group constituted by: silver, arsenic, selenium, germanium, and gallium.
  • a subject matter of the present description is also a galvanic bath intended for the execution of a galvanic electrodeposition process (of the type just described).
  • This galvanic bath comprises an aqueous solution and is adapted to coat with a layer of yellow gold alloy at least one object immersed in said solution.
  • the aqueous solution comprises at least:
  • the bath according to the invention can comprise one or more of the specifications related to the bath itself and to the aqueous solution described in the preceding paragraphs in relation to the galvanic electrodeposition process.
  • the aqueous solution thus comprises: gold in a quantity equal to 5 grams per liter of solution, copper in a quantity equal to 55 grams per liter of solution, indium and zinc in quantities (each) equal to 0.5 grams per liter of solution. Furthermore, in the electrodeposition process which uses a galvanic bath with the formulation indicated above said bath is kept at a constant temperature equal to 60 °C, the solution is kept at pH 10.5, and a current density equal to 0.5 A/dm 2 is applied. Moreover, said formulation is enriched with:
  • the present description also relates to a yellow gold alloy, which (preferably but not necessarily) is obtained indeed by means of the process and/or the bath described in the preceding pages.
  • said alloy comprises at least:
  • the yellow gold alloy comprises:
  • the alloy comprises:
  • the present description also relates to the use of a gold alloy as described in the preceding paragraphs to provide self-supporting shells which can be used in particular in the fields of clothing, jewelry, costume jewelry, shoes and leatherwear (and other sectors such as fashion, faucets, eyewear and also electronics).
  • the process provides, according to per se traditional manners, for applying a potential difference to the electrodes immersed in the galvanic bath, wherein the object (each object) to be coated with a protective layer acts as a cathode.
  • the object each object to be coated with a protective layer acts as a cathode.
  • One of the particularities of the invention which allows to overcome the limitations of known processes, is indeed the composition of the aqueous solution of the bath (in which the object to be coated is indeed immersed).
  • aqueous solution of which comprises (in the indicated ranges) gold and copper in the form of alkaline cyanides, indium and zinc in the form of soluble compounds in fact allows to deposit a layer of quaternary gold alloy (comprising gold, copper, indium and zinc) with high mechanical strength, both with low thicknesses and with high thicknesses, so as to be able to constitute a self-supporting shell (but also, if so desired, an effective coating layer).
  • quaternary gold alloy comprising gold, copper, indium and zinc
  • zinc in the form of a soluble complex is of extreme practical interest.
  • the obtained layer has high solderability, understood indeed as the capacity to withstand successive soldering treatments (which are for example necessary to close the openings provided in order to remove the internal core and indeed obtain the self-supporting shell).
  • the deposited layer is free from residual tensions, proving itself resilient (not fragile) and therefore capable of withstanding impacts and stresses without generating cracks and failures.
  • the invention is furthermore very versatile and allows to obtain yellow gold alloys with a number of carats comprised between for example 8 and 23.
  • the chosen composition ensures the capability to keep the fineness constant, as a further assurance of the reliability and repeatability of the process and of the strength of the alloy obtained.
  • the invention allows to obtain the results described above without using and without resorting to silver (except in traces or as a grain refiner or brightener) and especially without cadmium or other metals and substances that are potentially toxic, thereby revealing itself to be of extreme practical interest.
  • the materials used, as well as the dimensions, may be any according to the requirements and the state of the art.

Landscapes

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

Abstract

Procédé d'électrodéposition galvanique comprenant une étape consistant à revêtir, d'une couche d'alliage d'or jaune, au moins un objet immergé dans un bain galvanique contenant une solution aqueuse. La solution aqueuse comprend au moins : de l'or en une quantité comprise entre 1 gramme et 10 grammes par litre de solution, sous forme de cyanure alcalin ; du cuivre en une quantité comprise entre 30 grammes et 70 grammes par litre de solution, sous forme de composé de cyanure alcalin ; de l'indium en une quantité comprise entre 100 milligrammes et 2 grammes par litre de solution, sous forme de composé soluble ; du zinc en une quantité comprise entre 100 milligrammes et 2 grammes par litre de solution, sous forme de composé soluble.
EP21716861.6A 2021-02-23 2021-02-23 Procédé d'électrodéposition galvanique et bain galvanique associé Pending EP4298270A1 (fr)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
PCT/IT2021/000006 WO2022180650A1 (fr) 2021-02-23 2021-02-23 Procédé d'électrodéposition galvanique et bain galvanique associé

Publications (1)

Publication Number Publication Date
EP4298270A1 true EP4298270A1 (fr) 2024-01-03

Family

ID=75396836

Family Applications (1)

Application Number Title Priority Date Filing Date
EP21716861.6A Pending EP4298270A1 (fr) 2021-02-23 2021-02-23 Procédé d'électrodéposition galvanique et bain galvanique associé

Country Status (3)

Country Link
EP (1) EP4298270A1 (fr)
CN (1) CN116917549A (fr)
WO (1) WO2022180650A1 (fr)

Family Cites Families (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CH662583A5 (fr) 1985-03-01 1987-10-15 Heinz Emmenegger Bain galvanique pour le depot electrolytique d'alliages d'or-cuivre-cadmium-zinc.
US5085744A (en) 1990-11-06 1992-02-04 Learonal, Inc. Electroplated gold-copper-zinc alloys
GB9314292D0 (en) * 1993-07-10 1993-08-25 Johnson Matthey Plc Gold alloy
EP0904765A2 (fr) * 1997-09-25 1999-03-31 Ivoclar Ag Alliage dentaire de couleur d'or
DE60105987D1 (de) * 2001-05-30 2004-11-04 Leg Or S R L Goldlegierungen und Vorlegierungen zu deren Herstellung
EP1983077B1 (fr) 2007-04-19 2016-12-28 Enthone, Inc. Électrolyte et procédé pour le dépôt électrolytique d'alliages or-cuivre
ITFI20120208A1 (it) * 2012-10-12 2014-04-13 Bluclad S R L Soluzione per l'elettrodeposizione di una lega di oro e la lega da essa derivante.
DE102013109400A1 (de) * 2013-08-29 2015-03-05 Harting Kgaa Kontaktelement mit Goldbeschichtung

Also Published As

Publication number Publication date
WO2022180650A1 (fr) 2022-09-01
CN116917549A (zh) 2023-10-20

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