EP1881090A1 - Electrolyte composition und process for the deposition of a zinc-nickel alloy layer on a cast iron or steel substrate - Google Patents
Electrolyte composition und process for the deposition of a zinc-nickel alloy layer on a cast iron or steel substrate Download PDFInfo
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- EP1881090A1 EP1881090A1 EP06014519A EP06014519A EP1881090A1 EP 1881090 A1 EP1881090 A1 EP 1881090A1 EP 06014519 A EP06014519 A EP 06014519A EP 06014519 A EP06014519 A EP 06014519A EP 1881090 A1 EP1881090 A1 EP 1881090A1
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- electrolyte composition
- zinc
- substrate
- nickel
- alloy layer
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- 239000003792 electrolyte Substances 0.000 title claims abstract description 45
- 239000000203 mixture Substances 0.000 title claims abstract description 32
- 239000000758 substrate Substances 0.000 title claims abstract description 28
- 229910000990 Ni alloy Inorganic materials 0.000 title claims abstract description 20
- 239000010959 steel Substances 0.000 title claims abstract description 10
- QELJHCBNGDEXLD-UHFFFAOYSA-N nickel zinc Chemical compound [Ni].[Zn] QELJHCBNGDEXLD-UHFFFAOYSA-N 0.000 title claims description 21
- 229910001018 Cast iron Inorganic materials 0.000 title claims description 11
- 230000008021 deposition Effects 0.000 title claims description 11
- 238000000034 method Methods 0.000 title claims description 9
- 229910001208 Crucible steel Inorganic materials 0.000 title claims description 7
- DHMQDGOQFOQNFH-UHFFFAOYSA-N Glycine Chemical compound NCC(O)=O DHMQDGOQFOQNFH-UHFFFAOYSA-N 0.000 claims abstract description 19
- 229960002449 glycine Drugs 0.000 claims abstract description 8
- 235000013905 glycine and its sodium salt Nutrition 0.000 claims abstract description 8
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 claims abstract description 6
- 229910052700 potassium Inorganic materials 0.000 claims abstract description 3
- 239000011591 potassium Substances 0.000 claims abstract description 3
- 238000000151 deposition Methods 0.000 claims description 19
- WCUXLLCKKVVCTQ-UHFFFAOYSA-M Potassium chloride Chemical compound [Cl-].[K+] WCUXLLCKKVVCTQ-UHFFFAOYSA-M 0.000 claims description 17
- VMHLLURERBWHNL-UHFFFAOYSA-M Sodium acetate Chemical compound [Na+].CC([O-])=O VMHLLURERBWHNL-UHFFFAOYSA-M 0.000 claims description 7
- 239000001103 potassium chloride Substances 0.000 claims description 7
- 235000011164 potassium chloride Nutrition 0.000 claims description 7
- KGBXLFKZBHKPEV-UHFFFAOYSA-N boric acid Chemical compound OB(O)O KGBXLFKZBHKPEV-UHFFFAOYSA-N 0.000 claims description 6
- 239000004327 boric acid Substances 0.000 claims description 6
- SCVFZCLFOSHCOH-UHFFFAOYSA-M potassium acetate Chemical compound [K+].CC([O-])=O SCVFZCLFOSHCOH-UHFFFAOYSA-M 0.000 claims description 6
- 239000001632 sodium acetate Substances 0.000 claims description 5
- 235000017281 sodium acetate Nutrition 0.000 claims description 5
- 235000011056 potassium acetate Nutrition 0.000 claims description 3
- -1 potassium halide Chemical class 0.000 claims description 3
- USFZMSVCRYTOJT-UHFFFAOYSA-N Ammonium acetate Chemical compound N.CC(O)=O USFZMSVCRYTOJT-UHFFFAOYSA-N 0.000 claims description 2
- 239000005695 Ammonium acetate Substances 0.000 claims description 2
- 235000019257 ammonium acetate Nutrition 0.000 claims description 2
- 229940043376 ammonium acetate Drugs 0.000 claims description 2
- 239000003513 alkali Substances 0.000 claims 1
- 150000004820 halides Chemical class 0.000 claims 1
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 abstract description 18
- 229910052759 nickel Inorganic materials 0.000 abstract description 9
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 abstract description 5
- 229910052708 sodium Inorganic materials 0.000 abstract description 4
- 239000011734 sodium Substances 0.000 abstract description 4
- 229910000831 Steel Inorganic materials 0.000 abstract description 3
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 abstract description 2
- VEQPNABPJHWNSG-UHFFFAOYSA-N Nickel(2+) Chemical compound [Ni+2] VEQPNABPJHWNSG-UHFFFAOYSA-N 0.000 abstract 1
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 abstract 1
- PTFCDOFLOPIGGS-UHFFFAOYSA-N Zinc dication Chemical compound [Zn+2] PTFCDOFLOPIGGS-UHFFFAOYSA-N 0.000 abstract 1
- 229910001453 nickel ion Inorganic materials 0.000 abstract 1
- 238000000926 separation method Methods 0.000 abstract 1
- NLXLAEXVIDQMFP-UHFFFAOYSA-N Ammonia chloride Chemical compound [NH4+].[Cl-] NLXLAEXVIDQMFP-UHFFFAOYSA-N 0.000 description 14
- JIAARYAFYJHUJI-UHFFFAOYSA-L zinc dichloride Chemical compound [Cl-].[Cl-].[Zn+2] JIAARYAFYJHUJI-UHFFFAOYSA-L 0.000 description 9
- BWHOZHOGCMHOBV-BQYQJAHWSA-N trans-benzylideneacetone Chemical compound CC(=O)\C=C\C1=CC=CC=C1 BWHOZHOGCMHOBV-BQYQJAHWSA-N 0.000 description 8
- BWHOZHOGCMHOBV-UHFFFAOYSA-N Benzalacetone Natural products CC(=O)C=CC1=CC=CC=C1 BWHOZHOGCMHOBV-UHFFFAOYSA-N 0.000 description 7
- 235000019270 ammonium chloride Nutrition 0.000 description 7
- 238000005260 corrosion Methods 0.000 description 7
- 230000007797 corrosion Effects 0.000 description 7
- QMMRZOWCJAIUJA-UHFFFAOYSA-L nickel dichloride Chemical compound Cl[Ni]Cl QMMRZOWCJAIUJA-UHFFFAOYSA-L 0.000 description 7
- KBPLFHHGFOOTCA-UHFFFAOYSA-N 1-Octanol Chemical compound CCCCCCCCO KBPLFHHGFOOTCA-UHFFFAOYSA-N 0.000 description 6
- KJCVRFUGPWSIIH-UHFFFAOYSA-N 1-naphthol Chemical compound C1=CC=C2C(O)=CC=CC2=C1 KJCVRFUGPWSIIH-UHFFFAOYSA-N 0.000 description 6
- XAEFZNCEHLXOMS-UHFFFAOYSA-M potassium benzoate Chemical compound [K+].[O-]C(=O)C1=CC=CC=C1 XAEFZNCEHLXOMS-UHFFFAOYSA-M 0.000 description 6
- 229910021586 Nickel(II) chloride Inorganic materials 0.000 description 4
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 4
- 238000000576 coating method Methods 0.000 description 4
- 239000002351 wastewater Substances 0.000 description 4
- 229910052725 zinc Inorganic materials 0.000 description 4
- 239000011701 zinc Substances 0.000 description 4
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 3
- 229910052751 metal Inorganic materials 0.000 description 3
- 239000002184 metal Substances 0.000 description 3
- CVHZOJJKTDOEJC-UHFFFAOYSA-N saccharin Chemical compound C1=CC=C2C(=O)NS(=O)(=O)C2=C1 CVHZOJJKTDOEJC-UHFFFAOYSA-N 0.000 description 3
- 150000003839 salts Chemical class 0.000 description 3
- 238000004065 wastewater treatment Methods 0.000 description 3
- 239000011592 zinc chloride Substances 0.000 description 3
- 235000005074 zinc chloride Nutrition 0.000 description 3
- FPYUJUBAXZAQNL-UHFFFAOYSA-N 2-chlorobenzaldehyde Chemical compound ClC1=CC=CC=C1C=O FPYUJUBAXZAQNL-UHFFFAOYSA-N 0.000 description 2
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 2
- PVNIIMVLHYAWGP-UHFFFAOYSA-N Niacin Chemical compound OC(=O)C1=CC=CN=C1 PVNIIMVLHYAWGP-UHFFFAOYSA-N 0.000 description 2
- 230000002378 acidificating effect Effects 0.000 description 2
- 229910045601 alloy Inorganic materials 0.000 description 2
- 239000000956 alloy Substances 0.000 description 2
- 238000009826 distribution Methods 0.000 description 2
- 238000010348 incorporation Methods 0.000 description 2
- KZVLNAGYSAKYMG-UHFFFAOYSA-N pyridine-2-sulfonic acid Chemical compound OS(=O)(=O)C1=CC=CC=N1 KZVLNAGYSAKYMG-UHFFFAOYSA-N 0.000 description 2
- 230000001105 regulatory effect Effects 0.000 description 2
- 229940081974 saccharin Drugs 0.000 description 2
- 235000019204 saccharin Nutrition 0.000 description 2
- 239000000901 saccharin and its Na,K and Ca salt Substances 0.000 description 2
- YGSDEFSMJLZEOE-UHFFFAOYSA-N salicylic acid Chemical compound OC(=O)C1=CC=CC=C1O YGSDEFSMJLZEOE-UHFFFAOYSA-N 0.000 description 2
- HEMHJVSKTPXQMS-UHFFFAOYSA-M sodium hydroxide Inorganic materials [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 2
- 239000002253 acid Substances 0.000 description 1
- 230000004913 activation Effects 0.000 description 1
- 229910001508 alkali metal halide Inorganic materials 0.000 description 1
- 150000008045 alkali metal halides Chemical class 0.000 description 1
- 229910052793 cadmium Inorganic materials 0.000 description 1
- BDOSMKKIYDKNTQ-UHFFFAOYSA-N cadmium atom Chemical compound [Cd] BDOSMKKIYDKNTQ-UHFFFAOYSA-N 0.000 description 1
- 239000011248 coating agent Substances 0.000 description 1
- 230000000536 complexating effect Effects 0.000 description 1
- 239000008139 complexing agent Substances 0.000 description 1
- 239000004035 construction material Substances 0.000 description 1
- 238000011161 development Methods 0.000 description 1
- 230000018109 developmental process Effects 0.000 description 1
- 238000009713 electroplating Methods 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- LGQLOGILCSXPEA-UHFFFAOYSA-L nickel sulfate Chemical compound [Ni+2].[O-]S([O-])(=O)=O LGQLOGILCSXPEA-UHFFFAOYSA-L 0.000 description 1
- 229910000363 nickel(II) sulfate Inorganic materials 0.000 description 1
- 229960003512 nicotinic acid Drugs 0.000 description 1
- 235000001968 nicotinic acid Nutrition 0.000 description 1
- 239000011664 nicotinic acid Substances 0.000 description 1
- FJKROLUGYXJWQN-UHFFFAOYSA-N papa-hydroxy-benzoic acid Natural products OC(=O)C1=CC=C(O)C=C1 FJKROLUGYXJWQN-UHFFFAOYSA-N 0.000 description 1
- 238000007747 plating Methods 0.000 description 1
- 229960004889 salicylic acid Drugs 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 238000011144 upstream manufacturing Methods 0.000 description 1
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
- C25D3/565—Electroplating: Baths therefor from solutions of alloys containing more than 50% by weight of zinc
-
- C—CHEMISTRY; METALLURGY
- C23—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
- C23C—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; SURFACE TREATMENT OF METALLIC MATERIAL BY DIFFUSION INTO THE SURFACE, BY CHEMICAL CONVERSION OR SUBSTITUTION; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL
- C23C18/00—Chemical coating by decomposition of either liquid compounds or solutions of the coating forming compounds, without leaving reaction products of surface material in the coating; Contact plating
- C23C18/16—Chemical coating by decomposition of either liquid compounds or solutions of the coating forming compounds, without leaving reaction products of surface material in the coating; Contact plating by reduction or substitution, e.g. electroless plating
- C23C18/48—Coating with alloys
- C23C18/50—Coating with alloys with alloys based on iron, cobalt or nickel
Definitions
- the present invention relates to an electrolyte composition for depositing a zinc-nickel alloy layer on a substrate, particularly a cast iron or steel substrate.
- ammonium chloride-containing, low-acid baths for the deposition of zinc-nickel alloy layers allow the deposition of corrosion-resistant layers with nickel incorporation rates in the range of 10 to 15 mass%, but have the typical disadvantage of acidic electrolytes, often to produce uneven metal distributions in the layers.
- the ammonium ions present in the electrolyte are environmentally relevant and pollute the waste water strongly.
- the ammonium concentration in the waste water of electroplating plants are strictly regulated and subject to constant control. In order to comply with the regulatory requirements therefore complicated and expensive wastewater treatment must be carried out.
- Ammonium chloride-containing zinc-nickel electrolytes for depositing corresponding alloy layers are known, for example, from US Pat U.S. Patents US 4388160 and US 4765871 known.
- ammonium chloride-containing electrolyte based on nickel chloride or nickel sulfate as a nickel metal salt carrier.
- the aforementioned electrolytes typically have ammonium chloride in a concentration of up to 300 g / l, which necessitates extensive wastewater treatment.
- the zinc-nickel alloy layers deposited from such alkaline zinc-nickel electrolytes typically exhibit incorporation rates of 10 to 15 mass% nickel.
- a typical electrolyte of this kind as in the US 4765871 6 to 17 g / l of zinc, 0.8 to 2.3 g / l of nickel and 112 to 186 g / l of sodium or potassium hydroxide.
- an electrolyte composition for depositing a zinc-nickel alloy layer on a substrate which is characterized in that the electrolyte composition comprises aminoacetic acid.
- the electrolyte compositions according to the invention are based on an alkali metal halide, preferably a potassium halide, more preferably potassium chloride as conductive salt and furthermore have an acetate of the group consisting of sodium acetate, potassium acetate or ammonium acetate or mixtures thereof.
- an alkali metal halide preferably a potassium halide, more preferably potassium chloride as conductive salt and furthermore have an acetate of the group consisting of sodium acetate, potassium acetate or ammonium acetate or mixtures thereof.
- the electrolyte composition of the present invention has a molar acetate: aminoacetic acid ratio of about 0.35 to about 0.91.
- the electrolyte composition according to the invention comprises boric acid and a brightener system consisting of saccharin, benzalacetone, orthochlorobenzaldehyde, octanol ethoxylate and a potassium salt of a sulfopropylated polyalkoxylated naphthol.
- the brightener system preferably used comprises between 2 to 4 g / l of sodium saccharin, 0.025 to 0.2 g / l of benzalacetone, 0.006 to 0.01 g / l of orthochlorobenzaldehyde, 0.8 to 1.2 g / l of octanol ethoxylate and 2.5 to 3.2 g / l of potassium salt of the sulfopropylated polyalkoxylated naphthol.
- the brightener system may have 0.5 to 1.0 g / L pyridine sulfonic acid.
- the potassium chloride preferably used as the conductive salt in the electrolyte composition may be contained in the composition at a concentration of about 190 to 220 g / L.
- the aminoacetic acid added according to the invention may be present in a concentration of between 10 and 50 g / l, preferably approximately 30 g / l, in the electrolyte composition.
- the object is achieved by a method for depositing a zinc-nickel alloy layer on a substrate, in particular a cast iron or steel substrate, in which the substrate to be coated, in particular a cast iron or iron substrate under application of a current with the electrolyte composition according to the invention will be contacted.
- the temperature of the electrolyte composition between about 20 ° C and about 60 ° C, preferably between 30 ° C and 40 ° C.
- the current density to be set for the deposition of the layer can be adjusted between about 0.5 and about 5 A / dm 2 , preferably between 1.0 and 3.5 A / dm 2 .
- the pH of the electrolyte composition described herein is between 5 and 6.
- the pH of the electrolyte composition described herein is between 5 and 6.
- a current density between 0.5 and 1.0 A / dm 2 was set.
- the pH of the electrolyte composition was between 5 and 6.
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- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Materials Engineering (AREA)
- Metallurgy (AREA)
- Organic Chemistry (AREA)
- Electrochemistry (AREA)
- General Chemical & Material Sciences (AREA)
- Mechanical Engineering (AREA)
- Electroplating And Plating Baths Therefor (AREA)
- Electroplating Methods And Accessories (AREA)
Abstract
Description
Die vorliegende Erfindung betrifft eine Elektrolytzusammensetzung zur Abscheidung einer Zink-Nickel-Legierungsschicht auf einem Substrat, insbesondere einem Gußeisen- oder Stahlsubstrat.The present invention relates to an electrolyte composition for depositing a zinc-nickel alloy layer on a substrate, particularly a cast iron or steel substrate.
Zur Verbesserung der Oberflächeneigenschaften von Substraten insbesondere hinsichtlich ihres Korrosionswiderstandes werden diese mit galvanischen Überzügen beschichtet. Aus dem Stand der Technik sind eine Vielzahl von unterschiedlichen Beschichtungsverfahren zur Abscheidung unterschiedlichster Metallschichten auf Substratoberflächen bekannt. Aufgrund der Tatsache, daß Zink-Nickel-Legierungen einen verbesserten Korrosionsschutz gegenüber reinen Zinkschichten aufweisen, besteht ein starkes Interesse daran, Zink-Nickel-Legierungen zur Verbesserung des Korrosionswiderstandes auf Substratoberflächen abzuscheiden.To improve the surface properties of substrates, in particular with regard to their corrosion resistance, they are coated with galvanic coatings. The prior art discloses a multiplicity of different coating methods for depositing a wide variety of metal layers on substrate surfaces. Due to the fact that zinc-nickel alloys have improved corrosion protection over pure zinc layers, there is a strong interest in depositing zinc-nickel alloys on substrate surfaces to improve corrosion resistance.
Insbesondere um den gesteigerten Korrosionsschutzanforderungen auf Gußeisen- und Stahloberflächen und dem seitens der Automobil- und Flugzeugindustrie geforderten Verzicht auf Kadmium nachzukommen, wurden in den letzten Jahren unterschiedliche Verfahren zur Abscheidung von Zink-Nickel-Legierungsschichten auf solchen Substratoberflächen entwickelt. Gemeinsames Ziel dieser Entwicklungen war es, Zink-Nickel-Legierungen mit einem definierten Nickelanteil abzuscheiden. Mit den aus dem Stand der Technik bekannten Verfahren werden in der Regel Nickelanteile zwischen 10 bis 15% abgeschieden, was einen größtmöglichen Korrosionsschutz bietet.In particular, in order to meet the increased corrosion protection requirements for cast iron and steel surfaces and the waiver of cadmium demanded by the automotive and aerospace industries, different processes for the deposition of zinc-nickel alloy layers on such substrate surfaces have been developed in recent years. The common goal of these developments was to deposit zinc-nickel alloys with a defined nickel content. With the methods known from the prior art usually deposited nickel shares between 10 to 15%, which offers the greatest possible corrosion protection.
Um solche Zink-Nickel-Legierungen abzuscheiden, werden nach dem Stand der Technik im wesentlichen zwei unterschiedliche Elektrolyten verwendet. Diese sind zum einen alkalische Zink-Nickel-Legierungsbäder und zum anderen leichtsaure ammoniumchloridhaltige Bäder. Beide Badtypen weisen jedoch erhebliche Nachteile auf.In order to deposit such zinc-nickel alloys, essentially two different electrolytes are used in the prior art. These are on the one hand alkaline zinc-nickel alloy baths and on the other hand acidic ammonium chloride-containing baths. Both bath types, however, have significant disadvantages.
Bei der Anwendung alkalischer Bäder lassen sich nur niedrige Abscheidegeschwindigkeiten erreichen und es ergeben sich insbesondere Schwierigkeiten bei der Abscheidung auf Gußeisen- oder Stahlsubstraten. Ein weiterer Nachteil besteht darin, daß diese Bäder hohe Konzentrationen an stark komplexbildenden Stoffen enthalten, was zu einer Belastung der Abwässer mit diesen oftmals organischen Komplexbildnern führt und somit zusätzliche Abwasseraufbereitungsschritte erfordert.When using alkaline baths only low deposition rates can be achieved and there are difficulties especially in the deposition on cast iron or steel substrates. Another disadvantage is that these baths contain high concentrations of highly complexing substances, which leads to a pollution of the waste water with these often organic complexing agents and thus requires additional wastewater treatment steps.
Ammoniumchloridhaltige, leichtsaure Bäder zur Abscheidung von Zink-Nickel-Legierungsschichten ermöglichen zwar die Abscheidung korrosionsfester Schichten mit Nickeleinbauraten im Bereich von 10 bis 15 Massen-%, weisen aber den typischen Nachteil saurer Elektrolyten auf, oftmals ungleichmäßige Metallverteilungen in den Schichten zu erzeugen. Darüber hinaus sind die in den Elektrolyten befindlichen Ammoniumionen umweltrelevant und belasten die Abwässer stark. Die Ammoniumkonzentration in den Abwässern von Galvanobetrieben sind streng reguliert und unterliegen steter Kontrolle. Um den behördlichen Vorgaben Genüge zu leisten müssen daher aufwendige und teure Abwasserreinigungen vorgenommen werden. Ammoniumchloridhaltige Zink-Nickel-Elektrolyten zur Abscheidung entsprechender Legierungsschichten sind beispielsweise aus den
Aufgrund der allgemeinen schlechten Schichtdicken- und Legierungselementverteilung, die beim Einsatz solcher ammoniumchloridhaltiger Elektrolyten erzielt werden und der mit dem Einsatz von Ammoniumchlorid einhergehenden Abwasserproblematik, wurden alkalisch arbeitende Zink-Nickel-Elektrolyte entwickelt.Due to the general poor Schichtdicken- and alloy element distribution, which are achieved in the use of such ammonium chloride-containing electrolytes and associated with the use of ammonium chloride wastewater problem, alkaline zinc-nickel electrolytes have been developed.
Die aus solchen alkalischen Zink-Nickel-Elektrolyten abgeschiedenen Zink-Nickel-Legierungsschichten zeigen typischerweise Einbauraten von 10 bis 15 Massen-% Nickel.The zinc-nickel alloy layers deposited from such alkaline zinc-nickel electrolytes typically exhibit incorporation rates of 10 to 15 mass% nickel.
Ein typischer Elektrolyt dieser Art, wie er auch in der
Solche Elektrolyten erweisen sich jedoch als wenig geeignet für die Beschichtung von Gußeisen oder hochfesten Stählen, wie sie beispielsweise als Konstruktionsmaterialien für Bremssättel in der Automobilindustrie eingesetzt werden. Nur nach aufwendigen Oberflächenaktivierungsmaßnahmen und/oder vorgeschalteten Zinkabscheidungen lassen sich solche Materialien in hinreichender Qualität mit einer Zink-Nickel-Legierungsschicht aus einem alkalischen Elektrolyten abgeschieden beschichten. Neben diesen Problemen verringert aber auch die geringe Abscheidegeschwindigkeit das ökonomische Ergebnis solcher Beschichtungsverfahren.However, such electrolytes prove to be less suitable for the coating of cast iron or high strength steels, such as are used as construction materials for calipers in the automotive industry. Only after elaborate surface activation measures and / or upstream zinc deposits can such materials be deposited in sufficient quality with a zinc-nickel alloy layer deposited from an alkaline electrolyte. In addition to these problems, however, the low deposition rate also reduces the economic result of such coating processes.
Aus der
Unter Berücksichtigung des zuvor Ausgeführten ist es daher die Aufgabe der vorliegenden Erfindung, eine Elektrolytzusammensetzung sowie ein Verfahren zur Abscheidung einer Zink-Nickel-Legierungsschicht auf einem Substrat, insbesondere einem Gußeisen- oder Stahlsubstrat, zur Verfügung zu stellen, welches die aus dem Stand der Technik bekannten Probleme zu überwinden vermag.In view of the above, it is therefore an object of the present invention to provide an electrolyte composition and a method for depositing a zinc-nickel alloy layer on a substrate, in particular a cast iron or steel substrate, which can overcome the problems known from the prior art.
Gelöst wird diese Aufgabe hinsichtlich der Elektrolytzusammensetzung durch eine Elektrolytzusammensetzung zur Abscheidung einer Zink-Nickel-Legierungsschicht auf einem Substrat welche dadurch gekennzeichnet ist, daß die Elektrolytzusammensetzung Aminoessigsäure aufweist.This object is achieved with respect to the electrolyte composition by an electrolyte composition for depositing a zinc-nickel alloy layer on a substrate which is characterized in that the electrolyte composition comprises aminoacetic acid.
Der Zusatz von Aminoessigsäure zu einem Zink und Nickel aufweisenden Elektrolyten führt überraschenderweise zur Abscheidung von Zink-Nickel-Legierungsschichten, welche einen Nickel-Anteil von 10 bis 18 Massen-% aufweisen und nahezu keine innere Spannung besitzen.The addition of aminoacetic acid to a zinc and nickel-containing electrolyte surprisingly leads to the deposition of zinc-nickel alloy layers, which have a nickel content of 10 to 18 mass% and have almost no internal stress.
Die erfindungsgemäßen Elektrolytzusammensetzungen basieren auf einem Alkalihalogenit, vorzugsweise einem Kaliumhalogenit, besonders bevorzugt Kaliumchlorid als Leitsalz und weisen darüber hinaus ein Acetat der Gruppe bestehend aus Natriumacetat, Kaliumacetat oder Ammoniumacetat oder Mischungen derselben auf.The electrolyte compositions according to the invention are based on an alkali metal halide, preferably a potassium halide, more preferably potassium chloride as conductive salt and furthermore have an acetate of the group consisting of sodium acetate, potassium acetate or ammonium acetate or mixtures thereof.
Die erfindungsgemäße Elektrolytzusammensetzung weist ein molares Acetat: Aminoessigsäureverhältnis von etwa 0,35 bis etwa 0,91 auf.The electrolyte composition of the present invention has a molar acetate: aminoacetic acid ratio of about 0.35 to about 0.91.
Weiterhin weist die erfindungsgemäße Elektrolytzusammensetzung Borsäure und ein Glanzbildnersystem bestehend aus Saccharin, Benzalaceton, Orthochlorbenzaldehyd, Oktanolethoxylat sowie einem Kaliumsalz eines sulfopropylierten polyalkoxylierten Naphtols auf.Furthermore, the electrolyte composition according to the invention comprises boric acid and a brightener system consisting of saccharin, benzalacetone, orthochlorobenzaldehyde, octanol ethoxylate and a potassium salt of a sulfopropylated polyalkoxylated naphthol.
Hierbei kann die Konzentration der Borsäure in einem Bereich zwischen ungefähr 10 und 30, bevorzugt zwischen 15 bis 20 g/l liegen.Here, the concentration of boric acid in a range between about 10 and 30, preferably between 15 to 20 g / l.
Das bevorzugt eingesetzte Glanzbildnersystem weist zwischen 2 bis 4 g/l Natriumsaccharin, 0,025 bis 0,2 g/l Benzalaceton, 0,006 bis 0,01 g/l Orthochlorbenzaldehyd, 0,8 - 1,2 g/l Oktanolethoxylat sowie 2,5 bis 3,2 g/l Kaliumsalz des sulfopropylierten polyalkoxylierten Naphthols auf. Darüber hinaus kann das Glanzbildnersystem 0,5 bis 1,0 g/l Pyridinsulfonsäure aufweisen.The brightener system preferably used comprises between 2 to 4 g / l of sodium saccharin, 0.025 to 0.2 g / l of benzalacetone, 0.006 to 0.01 g / l of orthochlorobenzaldehyde, 0.8 to 1.2 g / l of octanol ethoxylate and 2.5 to 3.2 g / l of potassium salt of the sulfopropylated polyalkoxylated naphthol. In addition, the brightener system may have 0.5 to 1.0 g / L pyridine sulfonic acid.
Das bevorzugt als Leitsalz in der Elektrolytzusammensetzung eingesetzte Kaliumchlorid kann in einer Konzentration zwischen ungefähr 190 bis 220 g/l in der Zusammensetzung enthalten sein.The potassium chloride preferably used as the conductive salt in the electrolyte composition may be contained in the composition at a concentration of about 190 to 220 g / L.
Die erfindungsgemäß zugesetzte Aminoessigsäure kann in Abhängigkeit des Elektrolytsystems in einer Konzentration zwischen 10 bis 50 g/l, bevorzugt ca. 30 g/l in der Elektrolytzusammensetzung enthalten sein.Depending on the electrolyte system, the aminoacetic acid added according to the invention may be present in a concentration of between 10 and 50 g / l, preferably approximately 30 g / l, in the electrolyte composition.
Hinsichtlich des Verfahrens wird die Aufgabe durch ein Verfahren zur Abscheidung einer Zink-Nickel-Legierungsschicht auf einem Substrat, insbesondere einem Gußeisen- oder Stahlsubstrat gelöst, bei welchem das zu beschichtende Substrat, insbesondere ein Gußeisen- oder Eisensubstrat unter Anlegung eines Stroms mit der erfindungsgemäßen Elektrolytzusammensetzung kontaktiert wird.With regard to the method, the object is achieved by a method for depositing a zinc-nickel alloy layer on a substrate, in particular a cast iron or steel substrate, in which the substrate to be coated, in particular a cast iron or iron substrate under application of a current with the electrolyte composition according to the invention will be contacted.
Hierbei kann die Temperatur der Elektrolytzusammensetzung zwischen ca. 20°C und ca. 60°C, bevorzugt zwischen 30°C und 40°C betragen.Here, the temperature of the electrolyte composition between about 20 ° C and about 60 ° C, preferably between 30 ° C and 40 ° C.
Die zur Abscheidung der Schicht einzustellende Stromdichte kann zwischen ca. 0,5 und ca. 5 A/dm2, bevorzugt zwischen 1,0 und 3,5 A/dm2 eingestellt werden.The current density to be set for the deposition of the layer can be adjusted between about 0.5 and about 5 A / dm 2 , preferably between 1.0 and 3.5 A / dm 2 .
Die Erfindung soll beispielhaft anhand der nachfolgenden Ausführungsbeispiele erläutert werden, ohne daß sich die Erfindung jedoch auf diese beschränken läßt.The invention will be explained by way of example with reference to the following embodiments, but without the invention can be limited to this.
Ein Gußeisensubstrat wird bei einer Temperatur zwischen 33 und 36° C und bei einer eingestellten Stromdichte von 1,0 bis 3,5 A/dm2 mit einer Elektrolytzusammensetzung der nachfolgenden Art kontaktiert:
- Zinkchlorid:
- 60-70 g/l
- Nickelchlorid x 6 H20:
- 100 - 130 g/l
- Kaliumchlorid:
- 190 - 220 g/l
- Borsäure:
- 15 - 20 g/l
- Natriumacetat * 3H2O:
- 25 g/l
- Aminoessigsäure:
- 30 g/l
- Natriumsaccharin:
- 2 - 4 g/l
- Benzalaceton:
- 0,025 - 0,20 g/l
- Orthochlorbenzaldehyd:
- 0,006 - 0,01 g/l
- Oktanolethoxylat:
- 0,8 - 1,2 g/l
- Zinc chloride:
- 60-70 g / l
- Nickel chloride x 6 H20:
- 100-130 g / l
- Potassium chloride:
- 190-220 g / l
- boric acid:
- 15-20 g / l
- Sodium acetate * 3H 2 O:
- 25 g / l
- aminoacetic:
- 30 g / l
- sodium:
- 2 - 4 g / l
- benzalacetone:
- 0.025-0.20 g / l
- Orthochlorbenzaldehyd:
- 0.006 - 0.01 g / l
- Oktanolethoxylat:
- 0.8-1.2 g / l
Der pH-Wert der hier beschriebenen Elektrolytzusammensetzung liegt zwischen 5 und 6.The pH of the electrolyte composition described herein is between 5 and 6.
Ein Gußeisensubstrat wird bei einer Temperatur zwischen 33 und 36° C und bei einer eingestellten Stromdichte von 1,0 bis 3,5 A/dm2 mit einer Elektrolytzusammensetzung der nachfolgenden Art kontaktiert:
- Zinkchlorid:
- 60 - 70 g/l
- Nickelchlorid x 6 H20:
- 100 - 130 g/l
- Kaliumchlorid:
- 190 - 220 g/l
- Borsäure:
- 15 - 20 g/l
- Natriumacetat * 3H2O:
- 25 g/l
- Aminoessigsäure:
- 30 g/l
- Natriumsaccharin:
- 2 - 4 g/l
- Benzalacetone:
- 0,025 - 0,050 g/l
- Pyridinsulfonsäure:
- 0,5- 1,0 g/l
- Oktanolethoxylate:
- 0,8 - 1,2 g/l
- Zinc chloride:
- 60 - 70 g / l
- Nickel chloride x 6 H20:
- 100-130 g / l
- Potassium chloride:
- 190-220 g / l
- boric acid:
- 15-20 g / l
- Sodium acetate * 3H 2 O:
- 25 g / l
- aminoacetic:
- 30 g / l
- sodium:
- 2 - 4 g / l
- Benzalacetone:
- 0.025-0.050 g / l
- pyridinesulfonic:
- 0.5-1.0 g / l
- Oktanolethoxylate:
- 0.8-1.2 g / l
Der pH-Wert der hier beschriebenen Elektrolytzusammensetzung liegt zwischen 5 und 6.The pH of the electrolyte composition described herein is between 5 and 6.
Stahlsubstrate und Stahlsubstrate für das Trommelgalvanisieren wurden bei einer Temperatur zwischen 33 und 35°C mit einer Elektrolytzusammensetzung der nachfolgenden Art kontaktiert.
- Zinkchlorid:
- 60 - 76 g/l
- Nickelchlorid x 6 H20:
- 100 - 130 g/l
- Kaliumchlorid:
- 190 - 220 g/l
- Borsäure:
- 15 - 20 g/l
- Kaliumacetat:
- 25 g/l
- Aminoessigsäure:
- 30 g/l
- Natriumsaccharin:
- 2 - 4 g/l
- Benzalacetone:
- 0,025 - 0,050 g/l
- Orthochlorbenzaldehyd:
- 0,008 - 0,012 g/l
- Oktanolethoxylate:
- 0,8 - 1,2 g/l
- Zinc chloride:
- 60 - 76 g / l
- Nickel chloride x 6 H20:
- 100-130 g / l
- Potassium chloride:
- 190-220 g / l
- boric acid:
- 15-20 g / l
- potassium acetate:
- 25 g / l
- aminoacetic:
- 30 g / l
- sodium:
- 2 - 4 g / l
- Benzalacetone:
- 0.025-0.050 g / l
- Orthochlorbenzaldehyd:
- 0.008-0.012 g / l
- Oktanolethoxylate:
- 0.8-1.2 g / l
Hierbei wurde eine Stromdichte zwischen 0,5 und 1,0 A/dm2 eingestellt. Der pH-Wert der Elektrolytzusammensetzung lag zwischen 5 und 6.Here, a current density between 0.5 and 1.0 A / dm 2 was set. The pH of the electrolyte composition was between 5 and 6.
Claims (9)
Priority Applications (6)
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HUE06014519A HUE026918T2 (en) | 2006-07-13 | 2006-07-13 | Electrolyte composition und process for the deposition of a zinc-nickel alloy layer on a cast iron or steel substrate |
ES06014519.0T ES2553730T3 (en) | 2006-07-13 | 2006-07-13 | Electrolyte composition and procedure for the deposition of a layer of zinc-nickel alloy on a cast iron or cast steel substrate |
PL06014519T PL1881090T3 (en) | 2006-07-13 | 2006-07-13 | Electrolyte composition und process for the deposition of a zinc-nickel alloy layer on a cast iron or steel substrate |
EP06014519.0A EP1881090B1 (en) | 2006-07-13 | 2006-07-13 | Electrolyte composition und process for the deposition of a zinc-nickel alloy layer on a cast iron or steel substrate |
PT60145190T PT1881090E (en) | 2006-07-13 | 2006-07-13 | Electrolyte composition und process for the deposition of a zinc-nickel alloy layer on a cast iron or steel substrate |
US11/778,011 US8435398B2 (en) | 2006-07-13 | 2007-07-13 | Electrolyte composition and method for the deposition of a zinc-nickel alloy layer on a cast iron or steel substrate |
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EP06014519.0A EP1881090B1 (en) | 2006-07-13 | 2006-07-13 | Electrolyte composition und process for the deposition of a zinc-nickel alloy layer on a cast iron or steel substrate |
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Country | Link |
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US (1) | US8435398B2 (en) |
EP (1) | EP1881090B1 (en) |
ES (1) | ES2553730T3 (en) |
HU (1) | HUE026918T2 (en) |
PL (1) | PL1881090T3 (en) |
PT (1) | PT1881090E (en) |
Cited By (1)
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DE102008007133A1 (en) * | 2008-01-31 | 2009-08-06 | Metallveredelung Huber Gmbh | Coating for galvanically applying on fittings as corrosion support, comprises a first alkaline zinc layer applied on raw material, a second acid zinc-nickel layer applied on the zinc layer, and a transparent passivation |
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FR2956123B1 (en) * | 2010-02-08 | 2017-10-27 | Dalic | METHOD FOR PROTECTING A METAL SUBSTRATE AGAINST CORROSION AND ABRASION, AND METAL SUBSTRATE OBTAINED BY THIS METHOD. |
EP2784188B2 (en) * | 2013-03-26 | 2018-04-25 | ATOTECH Deutschland GmbH | Process for corrosion protection of iron containing materials |
CN104651888B (en) * | 2015-03-04 | 2017-03-22 | 武汉风帆电化科技股份有限公司 | High corrosion resistance zinc-nickel alloy electroplating additive with weak acidity to neutrality and electroplating liquid |
Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
SU524866A1 (en) * | 1975-04-10 | 1976-08-15 | Предприятие П/Я А-7697 | Electrolyte for deposition of zinc-nickel alloys |
GB1498212A (en) * | 1974-03-18 | 1978-01-18 | Mcgean Chem Co Inc | Electroplating bath for producing zinc-copper alloys |
US4861442A (en) * | 1988-02-26 | 1989-08-29 | Okuno Chemical Industries Co., Ltd. | Zinc-nickel alloy plating bath and plating method |
US5718745A (en) * | 1995-08-09 | 1998-02-17 | Japan Kanigen Co., Ltd. | Electroless plating bath for forming black coatings and process for forming the coatings |
EP1295967A2 (en) * | 2001-09-21 | 2003-03-26 | Enthone Inc. | Process for depositing a zinc-nickel alloy from an electrolyte |
Family Cites Families (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4146441A (en) * | 1977-10-06 | 1979-03-27 | R. O. Hull & Company, Inc. | Additive compositions, baths, and methods for electrodepositing bright zinc deposits |
US4388160A (en) * | 1980-02-20 | 1983-06-14 | Rynne George B | Zinc-nickel alloy electroplating process |
US4765871A (en) * | 1981-12-28 | 1988-08-23 | The Boeing Company | Zinc-nickel electroplated article and method for producing the same |
US4543166A (en) * | 1984-10-01 | 1985-09-24 | Omi International Corporation | Zinc-alloy electrolyte and process |
US4825009A (en) * | 1985-12-23 | 1989-04-25 | Shell Oil Company | Preparation of nonionic surfactants |
US4832802A (en) * | 1988-06-10 | 1989-05-23 | Mcgean-Rohco, Inc. | Acid zinc-nickel plating baths and methods for electrodepositing bright and ductile zinc-nickel alloys and additive composition therefor |
US6238542B1 (en) * | 1998-09-15 | 2001-05-29 | Thomas Helden | Water soluble brighteners for zinc and zinc alloy electrolytes |
CN101273157A (en) * | 2005-06-20 | 2008-09-24 | 百富可公司 | Zinc-nickel alloy electroplating system |
-
2006
- 2006-07-13 EP EP06014519.0A patent/EP1881090B1/en active Active
- 2006-07-13 HU HUE06014519A patent/HUE026918T2/en unknown
- 2006-07-13 ES ES06014519.0T patent/ES2553730T3/en active Active
- 2006-07-13 PL PL06014519T patent/PL1881090T3/en unknown
- 2006-07-13 PT PT60145190T patent/PT1881090E/en unknown
-
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- 2007-07-13 US US11/778,011 patent/US8435398B2/en active Active
Patent Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB1498212A (en) * | 1974-03-18 | 1978-01-18 | Mcgean Chem Co Inc | Electroplating bath for producing zinc-copper alloys |
SU524866A1 (en) * | 1975-04-10 | 1976-08-15 | Предприятие П/Я А-7697 | Electrolyte for deposition of zinc-nickel alloys |
US4861442A (en) * | 1988-02-26 | 1989-08-29 | Okuno Chemical Industries Co., Ltd. | Zinc-nickel alloy plating bath and plating method |
US5718745A (en) * | 1995-08-09 | 1998-02-17 | Japan Kanigen Co., Ltd. | Electroless plating bath for forming black coatings and process for forming the coatings |
EP1295967A2 (en) * | 2001-09-21 | 2003-03-26 | Enthone Inc. | Process for depositing a zinc-nickel alloy from an electrolyte |
Non-Patent Citations (1)
Title |
---|
DATABASE WPI Section Ch Week 197723, Derwent World Patents Index; Class M11, AN 1977-41161Y, XP002411924, "Electrolytic plate zinc nickel alloy steel contain acetic acid salt add amino" * |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE102008007133A1 (en) * | 2008-01-31 | 2009-08-06 | Metallveredelung Huber Gmbh | Coating for galvanically applying on fittings as corrosion support, comprises a first alkaline zinc layer applied on raw material, a second acid zinc-nickel layer applied on the zinc layer, and a transparent passivation |
Also Published As
Publication number | Publication date |
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US8435398B2 (en) | 2013-05-07 |
EP1881090B1 (en) | 2015-09-16 |
HUE026918T2 (en) | 2016-07-28 |
PT1881090E (en) | 2015-12-01 |
PL1881090T3 (en) | 2016-03-31 |
ES2553730T3 (en) | 2015-12-11 |
US20080110762A1 (en) | 2008-05-15 |
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