EP1114206A1 - Bain alcalin aqueux exempt de cyanure s'utilisant pour le depot par galvanisation de revetements en zinc ou en alliage de zinc - Google Patents

Bain alcalin aqueux exempt de cyanure s'utilisant pour le depot par galvanisation de revetements en zinc ou en alliage de zinc

Info

Publication number
EP1114206A1
EP1114206A1 EP99936607A EP99936607A EP1114206A1 EP 1114206 A1 EP1114206 A1 EP 1114206A1 EP 99936607 A EP99936607 A EP 99936607A EP 99936607 A EP99936607 A EP 99936607A EP 1114206 A1 EP1114206 A1 EP 1114206A1
Authority
EP
European Patent Office
Prior art keywords
zinc
bath
bath according
amount
coatings
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.)
Granted
Application number
EP99936607A
Other languages
German (de)
English (en)
Other versions
EP1114206B1 (fr
Inventor
Birgit Sonntag
Udo Grieser
Barrie Sydney James
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.)
Atotech Deutschland GmbH and Co KG
Original Assignee
Atotech Deutschland GmbH and Co KG
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 Atotech Deutschland GmbH and Co KG filed Critical Atotech Deutschland GmbH and Co KG
Publication of EP1114206A1 publication Critical patent/EP1114206A1/fr
Application granted granted Critical
Publication of EP1114206B1 publication Critical patent/EP1114206B1/fr
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

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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
    • C25D3/22—Electroplating: Baths therefor from solutions of zinc
    • 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

Definitions

  • Cyanide-free zinc electrolyte baths can be divided into two bath types, namely weakly acidic zinc electrolytes (containing zinc chloride or zinc sulfate) and alkaline zincate electrolytes.
  • a uniformly shiny zinc layer is deposited from weakly acidic zinc baths, so that this process could quickly assert a strong market share.
  • this method has the disadvantage that its current efficiency is always 100% over a wide current density range.
  • the ratio of zinc layer thickness in the high current density range to zinc layer thickness in the low current density range is called the layer thickness distribution and should ideally be 1.
  • Zinc and zinc alloy baths have to meet ever higher demands. Accordingly, a zinc layer on the object to be coated should have the same layer thickness everywhere and have a high gloss.
  • a good layer thickness distribution can be achieved by lowering the current efficiency in the high current density range, while maintaining the current efficiency in the low current density range.
  • Alkaline zinc plating baths are generally based on an aqueous solution of zinc ions in sodium or potassium hydroxide. The use of these baths makes it possible to deposit zinc layers with a high gloss (DE 25 25 264, US 3 884 774), but these zinc layers do not have a uniform layer thickness distribution.
  • No. 5,435,898 describes a similar compound with the trade name Mirapol WT as an additive for zinc and zinc alloy electroplating baths, which is also said to greatly improve the layer thickness distribution.
  • DE 195 09 713 describes a diallylammonium sulfur dioxide copolymer as an additive for zinc and zinc alloy plating baths, which is intended to give the zinc layer a uniform layer thickness.
  • US Pat. No. 4,030,987 likewise describes a diallylammonium-sulfur dioxide copolymer as an additive for zinc and zinc alloy electroplating baths, which is intended to give the zinc layer a uniform layer thickness.
  • the invention is therefore based on the object of overcoming the shortcomings of the prior art and, in particular, of providing an aqueous cyanide-free alkaline bath for the electrodeposition of zinc and zinc alloy coatings, with which coatings of zinc or zinc alloys can be obtained, in which even after prolonged use Storage there is no tendency to form flaking.
  • the advantages of these baths with regard to a uniform layer thickness, a high gloss and the uniformity of the alloy components in the coating are to be maintained over a wide range of current densities. It has now been found that the addition of a special type of quaternary ammonium polymer to aqueous alkaline cyanide-free zinc baths improves the layer thickness distribution of the coatings obtained and reduces the blistering of the coatings.
  • the invention therefore relates to an aqueous alkaline, cyano-free bath for the galvanic deposition of zinc or zinc alloy coatings on substrate surfaces, which is characterized in that it
  • n is 2 or 3
  • n is at least 2
  • R x , R 2 , R 3 and R which may be the same or different, each represent methyl, ethyl, hydroxyethyl
  • p is in the range of 3 to 12 and X "stands for Cl “ , Br “ and / or I "
  • the soluble polymer of the general formula A contained in the bath according to the invention can be obtained by reacting N, N'-bis [3- (Dialkylamino) alkyl] ureas with 1, ⁇ -Dihaiogenalkanen he will keep.
  • This reaction can be represented by the following reaction scheme, where the radicals R ! -R 4 , X and m and n are as defined above:
  • the reaction of the starting products can be carried out, for example, in aqueous solution and at temperatures of 20 to 100 ° C.
  • the polymers of formula A used according to the invention can be obtained in which the amino urea units are connected by hydrocarbon bridges.
  • the degree of polymerization of these polymers is 2-80.
  • the starting materials of the general formulas D and E are known per se.
  • the diaminoureas of the formula D are described, for example, in JP 04-198160.
  • the other starting products for the preparation of the polymers used according to the invention are l, ⁇ -dihaloalkanes of the general formula E. Individual examples of these l, ⁇ -dihaloalkanes are 1,3-dichloropropane, 1,4-dichlorobutane, 1,5-di- chloropentane, 1, 6-dichlorohexane.
  • the polymer of formula A is contained in the bath according to the invention in an amount of 0.1 to 50 g / 1, preferably 0.25 to 10 g / 1.
  • the degree of polymerization of polymer A plays no role in avoiding the formation of bubbles and improving the layer thickness distribution; only the required solubility of the polymer in the galvanic bath places an upper limit on the degree of polymerization.
  • the bath contains as a further additive a quaternary derivative of a pyridine-3-carboxylic acid of the formula B and / or a quaternary derivative of a pyridine-3-carboxylic acid of the formula C.
  • R 6 is a saturated or unsaturated, aliphatic, aromatic or araliphatic hydrocarbon radical having 1 to 12 carbon atoms.
  • the amount of this additional additive in the bath according to the invention is 0.005 to 0.5 g / l, preferably 0.01 to 0.2 g / l.
  • the quaternary derivatives of a pyridine-3-carboxylic acid of Formula 3 or C are used as further additives in the inventive bath are compounds known per se and at ⁇ play, in BS James, M Phil Thesis, Aston University. 1979 or DE 40 38 721. These derivatives are generally prepared by reacting nicotinic acid with aliphatic, aromatic or araliphatic hydrogen halides.
  • the baths according to the invention can also contain further polymers, such as, for example, the polymers mentioned in the abovementioned publications.
  • the cyanide-free zinc baths according to the invention correspond to the customary aqueous alkaline cyanide-free baths, such as those used for the deposition of zinc or Zinc alloy coatings can be used on various substrates. Standard baths of this type are described, for example, in DE 25 25 264 and US 3,884,774.
  • the baths according to the invention contain the usual sources of zinc ions, such as zinc metal, zinc salts and zinc oxide, but preference is given to zinc oxide which is present as zincate in alkaline solution.
  • the concentration of the zinc in the baths according to the invention is in the range of 0.2 to 20 g / 1, preferably 5 to 20 g / 1, which is customary for such baths.
  • the baths contain a source of additional metal ions.
  • additional metal ions cobalt, nickel, manganese and / or iron ions are preferred.
  • Salts of the corresponding metals, preferably of the metals described above, optionally also in a mixture, are preferably used as sources for these additional metal ions.
  • Suitable salts are nickel sulfate, iron sulfate, cobalt sulfate and manganese chloride.
  • the concentration of the metal ions in the baths according to the invention can vary within a wide range and is preferably 0.01 to 100 g / l. Since a different alloy content is required for different alloy types, for example to improve corrosion protection, this concentration differs from metal ion to metal ion.
  • the baths preferably contain zinc in an amount of 0.2 to 20 g / 1, cobalt in an amount of 10 to 120 mg / 1, nickel in an amount of 0.3 to 3 g / 1, manganese in an amount of 10 up to 100 g / 1 and iron in an amount of 10 to 120 mg / 1. These concentrations relate to the amount of metal ions contained in the bath. Corresponding conversions provide the amounts of the salts of these metals to be used in each case.
  • baths according to the invention contain the above-mentioned additional metal ions, then it is expedient to add complexing agents which are matched to these additional metal ions in order to control the deposition potentials and to enable a joint reduction with the zinc ions present.
  • Chelating agents are preferred as such complexing agents.
  • suitable chelating agents are hydroxycarboxylates, such as sodium gluconate, amino alcohols, such as triethanolamine, polyamines, such as polyethylene diamine, aminocarboxyates, such as ⁇ DTA, amine phosphonates, such as amino-tris (ethylene phosphonic acid), and polyhydric alcohols, such as sorbitol or sucrose.
  • the chelating agent can be contained individually or as a mixture in the 3-baths according to the invention, the amount of which is preferably in the range from 2 to 200 g / l.
  • the baths according to the invention like the corresponding baths of the prior art - contain a hydroxide ion source, preferably an alkali metal hydroxide.
  • a hydroxide ion source preferably an alkali metal hydroxide.
  • Sodium hydroxide is usually used in a concentration of 80 to 250 g / l; however, other alkali and alkaline earth metal hydroxides and mixtures thereof are also suitable for use in the bath according to the invention. So show by using e.g. Potassium hydroxide increases the gloss of the zinc layer.
  • the baths according to the invention can contain known levelers, such as 3-mercapto-1,2,4,4-triazole and / or thiourea, thiourea being preferred.
  • concentration of the leveler is the usual concentration of zinc baths and is, for example, 0.01 to 0.50 g / 1.
  • Other additives for the baths according to the invention are aromatic aldehydes or their bisulfite adducts.
  • Preferred aromatic aldehydes are selected from the group 4-hydroxybenzaldehyde, 4-hydroxy-3-methoxybenzaldehyde (vanillin), 3, 4-dimethoxybenzaldehyde, 3, 4-methylenedioxybenzaldehyde, 2-hydroxybenzaldehyde and 4-hydroxybenzaldehyde or mixtures thereof.
  • These additives the concentration of which is in the range from 0.005 to 1.0 g / 1, preferably from 0.01 to 0.50 g / 1, act in a manner known per se as brighteners.
  • a particularly preferred example of such a brightener is vanillin.
  • the bath according to the invention can also act as a brightener, such as substances selected from the group consisting of sulfur compounds, aldehydes, ketones, amines, polyvinyl alcohol, polyvinyl pyrrolidone, proteins or reaction products of halohydrins with aliphatic or aromatic amines, polyamines or heterocyclic nitrogen compounds and mixtures thereof.
  • a brightener such as substances selected from the group consisting of sulfur compounds, aldehydes, ketones, amines, polyvinyl alcohol, polyvinyl pyrrolidone, proteins or reaction products of halohydrins with aliphatic or aromatic amines, polyamines or heterocyclic nitrogen compounds and mixtures thereof.
  • the baths according to the invention can also contain water-softening agents, since such additives reduce the sensitivity of the bath according to the invention to foreign metal ions, in particular calcium and magnesium from tap water.
  • water softening agents are EDTA, sodium silicates and tartaric acid.
  • conventional conductive substrates made of metal can be provided with a coating of zinc or a zinc alloy.
  • Another object of the invention is therefore a method for the galvanic deposition of zinc coatings or zinc alloy coatings on conventional substrates, which is characterized in that a bath with the above composition is used as the bath.
  • the coatings are preferably deposited at a current density in the range from 0.01 to 10 A / dm and at a temperature in the range from 15 to 45 ° C.
  • the method according to the invention can be carried out, for example, as a drum electroplating process and for deposition on larger workpieces as a rack electroplating process.
  • Anodes are used that can be soluble, such as zinc anodes, which also serve as a source of zinc ions, so that the zinc deposited on the cathode is recovered by dissolving zinc at the anode.
  • insoluble anodes such as, for example, iron anodes, can also be used, the zinc ions extracted from the electrolyte having to be added again in another way, for example using a zinc dissolving container.
  • the process according to the invention can also be operated with air blowing in, with movement of goods or without movement, without this resulting in any disadvantages for the coatings obtained.
  • Trilon D trisodium salt of hydroxyethylethylenediaminetriacetic acid; from BASF, 40% solution
  • a coated Zn anode serves as the anode. It works with strong air injection (1 1 / min), which flows out of an L-shaped plastic tube with 6 small holes (3 on each side) below the inserted cathode.
  • the cathode sheet (18.5 cm x 5 cm) is bent at the lower end and coated at 2.8 A for 35 min.
  • the bath should have a temperature of 20 ° C, as bubbles occur especially at low temperatures.
  • the sheet is rinsed off, lightened for 10 s in 0.3% by volume of HNO 3 , rinsed again and dried under compressed air. Then the sheet is carefully bent straight until it takes on an elongated shape and stored at room temperature. It must be checked daily for blisters.
  • the cathode sheet is coated at 1A for 15 minutes.
  • the bath should have a temperature of 28 ° C.
  • the sheet is rinsed off, lightened for 10 s in 0.3% by volume of HNO 3 , rinsed again and dried under compressed air.
  • the layer thickness is measured at two points 3 cm from the bottom
  • the layer thickness distribution corresponds to the ratio of the measured values for the layer thickness at high (hcd) and low current density (icd).
  • a bath with the following composition is used:
  • the layer thickness measurement is carried out at two points 3 cm from the lower edge and 2.5 cm from the right and left side edge at high (2.8 A / dm 2 ) and low current density (0.5 A / dm).
  • XRF is used to measure at four points at the respective position in order to keep the measurement error as low as possible.
  • the layer thickness distribution corresponds to the ratio of the measured values for the layer thickness at high (hcd) and low current density (Icd).
  • Trilon D trisodium salt of hydroxyethylethylenediaminetriacetic acid; from BASF, 40% solution
  • aqueous electrolyte was produced which is suitable for the galvanic deposition of a zinc layer.
  • the electrolyte had the following composition: 10 g / 1 ZnO 120 g / 1 KOH
  • a steel sheet (5 cm x 5 cm) was deposited at 2 A / dm and 30 ° C for 30 minutes.
  • the steel sheet was rinsed and chromated in a commercially available blue chromating (Corrotriblue, Atotech).
  • the chromated sheet had a standard commercially available.
  • the zinc layer showed no tendency to form bubbles, even tempering in a circulating air cabinet at 220 ° C for 30 minutes and subsequent quenching in tap water at room temperature did not lead to flaking.
  • aqueous electrolyte was produced which is suitable for the galvanic deposition of a zinc layer.
  • the electrolyte had the following composition:
  • the Hull cell sheet was rinsed and chromatized in a commercially available yellow chromation (Tridur Yellow Liquid, Atot ⁇ ch).
  • the chromated sheet had a slight iridescence and standard commercially available.
  • the layer thickness distribution was measured according to the test described above, it was 1.30.
  • the zinc layer showed no signs of blistering, even after 30 minutes in the circulating air cabinet at 220 ° C. and subsequent quenching in tap water from room temperature.
  • aqueous electrolyte was produced which is suitable for the galvanic deposition of a zinc layer.
  • the electrolyte had the following composition:
  • Steel screws were galvanized in a drum with a current density of 0.1 - 1 A / dm and room temperature.
  • aqueous electrolyte was produced which is suitable for the galvanic deposition of a zinc-nickel layer.
  • the electrolyte had the following composition:
  • a steel sheet (5 cm x 5 cm) was deposited at 3 A / dm 2 and 30 ° C for 30 minutes.
  • a uniform, shiny zinc-nickel layer was deposited.
  • the zinc-nickel layer showed no signs of blistering, even after 30 minutes of tempering in a circulating air cabinet at 220 ° C. and subsequent quenching in tap water at room temperature.
  • aqueous electrolyte was produced which is suitable for the galvanic deposition of a zinc-iron layer.
  • the electrolyte had the following composition:
  • a steel sheet (5 cm x 5 cm) was deposited at 2 A / dm "and room temperature for 30 minutes. A uniform, shiny zinc-iron-cobalt layer was deposited.
  • the zinc-iron-cobalt layer showed no sign of blistering, even after 30 minutes of tempering in a circulating air cabinet at 220 ° C. and subsequent quenching in tap water at room temperature.
  • aqueous electrolyte was produced which is suitable for the galvanic deposition of a zinc-manganese layer.
  • the electrolyte had the following composition:
  • a Hullzellbl ⁇ ch was deposited at 1 ampere and room temperature for 15 minutes.
  • the Hull cell sheet was rinsed and lightened in 0.3 vol% HN0 3 for 10 s.
  • the layer thickness distribution was measured according to the test described above; it was 1.41.
  • the manganese incorporation was measured with XRF at the same positions at which the layer thickness was also measured. at 60 mg / 1 iron (as FeSC 4 • 7 H 2 0) 25 g / 1 sodium gluconate
  • a Hull cell sheet was deposited at 1 amp and room temperature for 15 minutes.
  • the Hull cell sheet was rinsed and chromated in a commercially available black chromation for zinc-iron layers (Tridur Schwarz Liquid ZnFe, Atot ⁇ ch).
  • the chromated sheet had a very good black color.
  • the layer thickness distribution was measured according to the test described above, it was 1.50.
  • the zinc-iron layer showed no signs of blistering, not even after 30 minutes' tempering in a circulating air cabinet at 220 ° C. and subsequent quenching in tap water at room temperature.
  • aqueous electrolyte was produced which is suitable for the galvanic deposition of a zinc-iron-cobalt layer.
  • the electrolyte had the following composition:
  • a bath with the following composition is used:
  • the layer thickness is measured at two points 3 cm from the lower edge and 2.5 cm from the right and left side edge at high (2.8 A / dm " ) and low current density (0.5 A / dm). Measurements are also taken XRF at four positions at the respective position in order to keep the measurement error as low as possible
  • the layer thickness distribution corresponds to the ratio of the measured values for the layer thickness at higher (hcd) and lower current density (icd).
  • a bath with the following composition is used:
  • A.l's anode is a coated Zn anode. It will be at strong air injection (1 1 / min) worked, which flows out of an L-shaped plastic tube with 6 ki ⁇ in ⁇ n holes (3 on each side) below the inserted cathode.
  • the cathode sheet (18.5 cm x 5 cm) is bent at the lower end and coated at 2.8 A for 35 min.
  • the bath should have a temperature of 20 ° C, since bubbles occur especially at low temperatures.
  • the sheet is rinsed off, lightened for 10 s in 0.3% by volume of HNO 3 , rinsed again and dried under compressed air. Thereafter, the sheet is carefully straightened until it assumes an elongated shape and stored at room temperature. It must be examined daily for blisters.

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  • 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)
  • Pyridine Compounds (AREA)
  • Electrodes For Compound Or Non-Metal Manufacture (AREA)
EP99936607A 1998-09-02 1999-07-26 Bain alcalin aqueux exempt de cyanure s'utilisant pour le depot par galvanisation de revetements en zinc ou en alliage de zinc Expired - Lifetime EP1114206B1 (fr)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
DE19840019A DE19840019C1 (de) 1998-09-02 1998-09-02 Wäßriges alkalisches cyanidfreies Bad zur galvanischen Abscheidung von Zink- oder Zinklegierungsüberzügen sowie Verfahren
DE19840019 1998-09-02
PCT/EP1999/005318 WO2000014305A1 (fr) 1998-09-02 1999-07-26 Bain alcalin aqueux exempt de cyanure s'utilisant pour le depot par galvanisation de revetements en zinc ou en alliage de zinc

Publications (2)

Publication Number Publication Date
EP1114206A1 true EP1114206A1 (fr) 2001-07-11
EP1114206B1 EP1114206B1 (fr) 2003-02-26

Family

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Family Applications (1)

Application Number Title Priority Date Filing Date
EP99936607A Expired - Lifetime EP1114206B1 (fr) 1998-09-02 1999-07-26 Bain alcalin aqueux exempt de cyanure s'utilisant pour le depot par galvanisation de revetements en zinc ou en alliage de zinc

Country Status (9)

Country Link
US (1) US6652728B1 (fr)
EP (1) EP1114206B1 (fr)
JP (1) JP4263363B2 (fr)
AT (1) ATE233329T1 (fr)
CA (1) CA2342219C (fr)
DE (2) DE19840019C1 (fr)
ES (1) ES2193728T3 (fr)
PT (1) PT1114206E (fr)
WO (1) WO2000014305A1 (fr)

Cited By (4)

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Publication number Priority date Publication date Assignee Title
LT5481B (lt) 2006-07-11 2008-03-26 Chemijos Institutas Šarminis cinko-kobalto lydinio dangų nusodinimo elektrolitas
EP2096193A1 (fr) 2008-02-21 2009-09-02 Atotech Deutschland Gmbh Processus de préparation de zinc résistant à la corrosion et linéair platiné en zinc-nickel ou pièces formées complexes
CN102171386A (zh) * 2008-10-17 2011-08-31 麦克德米德股份有限公司 锌合金的电镀浴及方法
US9322107B2 (en) 2009-09-08 2016-04-26 Atotech Deutschland Gmbh Polymers having terminal amino groups and use thereof as additives for zinc and zinc alloy electrodeposition baths

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DE10026956A1 (de) * 2000-05-30 2001-12-13 Walter Hillebrand Galvanotechn Zink-Legierungsbad
GB0017741D0 (en) * 2000-07-20 2000-09-06 Macdermid Canning Plc Zinc and zinc alloy electroplating additives and electroplating methods
JP2003049282A (ja) * 2001-08-06 2003-02-21 Hitachi Ltd 車載電装品及び電機機械並びにそれらの製造法
US6790265B2 (en) * 2002-10-07 2004-09-14 Atotech Deutschland Gmbh Aqueous alkaline zincate solutions and methods
US6830674B2 (en) * 2002-11-05 2004-12-14 Columbia Chemical Corporation Brightener additive and bath for alkaline cyanide-free zinc electroplating
US8377283B2 (en) * 2002-11-25 2013-02-19 Coventya, Inc. Zinc and zinc-alloy electroplating
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US7442286B2 (en) 2004-02-26 2008-10-28 Atotech Deutschland Gmbh Articles with electroplated zinc-nickel ternary and higher alloys, electroplating baths, processes and systems for electroplating such alloys
US7964083B2 (en) * 2004-03-04 2011-06-21 Taskem, Inc. Polyamine brightening agent
CZ300264B6 (cs) * 2004-08-02 2009-04-01 Atotech Cz, A.S. Dusíkatá polymerní prísada pro elektrolytické vylucování zinku a slitin zinku, zpusob její výroby a její použití
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ATE429528T1 (de) * 2005-04-26 2009-05-15 Atotech Deutschland Gmbh Alkalisches galvanikbad mit einer filtrationsmembran
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DE102005060030A1 (de) 2005-12-15 2007-06-21 Coventya Gmbh Quervernetzte Polymere, diese enthaltende Galvanisierungsbäder sowie deren Verwendung
EP1870495A1 (fr) * 2006-06-21 2007-12-26 Atotech Deutschland Gmbh Bain aqueux alcalin, exempt de cyanide, pour la déposition galvanique de couches de Zinc et alliages de Zinc
US8691346B2 (en) * 2008-05-09 2014-04-08 Birchwood Laboratories, Inc. Methods and compositions for coating aluminum substrates
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EP2175048A1 (fr) 2008-10-13 2010-04-14 Atotech Deutschland Gmbh Composition de placage métallique pour le dépôt d'alliages d'étain et de zinc sur un substrat
JP4849186B2 (ja) * 2009-10-28 2012-01-11 Ｊｆｅスチール株式会社 熱間プレス部材およびその製造方法
JP5630692B2 (ja) * 2010-07-20 2014-11-26 日本表面化学株式会社 亜鉛−鉄合金めっき液
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JP5551094B2 (ja) * 2011-01-31 2014-07-16 ディップソール株式会社 アルカリ性亜鉛及び亜鉛合金めっき浴
EP2489763A1 (fr) 2011-02-15 2012-08-22 Atotech Deutschland GmbH Matériau de couche d'alliage de zinc et de fer
CN105908226B (zh) 2011-06-07 2018-07-17 杰富意钢铁株式会社 热压用钢板
JP5747359B2 (ja) * 2012-10-09 2015-07-15 ユケン工業株式会社 ジンケート型亜鉛系めっき浴、ジンケート型亜鉛系めっき浴用添加剤および亜鉛系めっき部材の製造方法
IN2015DN02108A (fr) 2012-10-31 2015-08-14 Jfe Steel Corp
EP2784189A1 (fr) 2013-03-28 2014-10-01 Coventya SAS Bain d'électrodéposition d'alliages zinc-fer, procédé de dépôt d'alliage zinc-fer sur un dispositif et ledit dispositif
EP2801640A1 (fr) 2013-05-08 2014-11-12 ATOTECH Deutschland GmbH Bain électrolytique de nickel galvanique ou d'alliage de nickel pour déposer un alliage de nickel ou de nickel mi-lustré
CN103320821B (zh) * 2013-07-12 2016-08-10 贵阳华科电镀有限公司 一种碱性锌钴合金电镀液
CN105683250B (zh) * 2013-11-06 2019-04-12 罗门哈斯电子材料有限责任公司 作为调平剂的含氮聚合物
CN103952733B (zh) * 2013-12-23 2017-06-20 韶关美妥维志化工有限公司 用于碱性镀锌或锌合金电镀液中的载体光亮剂前体及载体光亮剂和电镀液
WO2016001317A1 (fr) 2014-07-04 2016-01-07 Basf Se Additif pour zingage alcalin
US10718060B2 (en) 2015-06-25 2020-07-21 Basf Se Additive for alkaline zinc plating
CN109642337B (zh) * 2016-05-24 2021-07-13 科文特亚股份有限公司 三元锌-镍-铁合金和用于电镀这种合金的碱性电解液
JP7002548B2 (ja) * 2016-12-22 2022-01-20 カール・フロイデンベルク・カー・ゲー 金属ピース品の表面に亜鉛含有皮膜を析出させるための水性アルカリ電解液
CN107513733A (zh) * 2017-09-08 2017-12-26 湖北吉和昌化工科技有限公司 一种新的无氰碱性镀锌配位剂
US11661666B2 (en) * 2019-10-10 2023-05-30 The Boeing Company Electrodeposited zinc and iron coatings for corrosion resistance
KR102173164B1 (ko) * 2020-05-20 2020-11-02 주식회사 지에스켐텍 징케이트 도금액용 혼합 광택제 및 이를 포함하는 징케이트 도금액
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CN121204749A (zh) * 2025-11-28 2025-12-26 山东力净环保科技有限公司 碱性体系多阶段电流-界面协同调控锌电极制备方法

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DE19840019C1 (de) 2000-03-16
JP2002524662A (ja) 2002-08-06
DE59904390D1 (de) 2003-04-03
WO2000014305A9 (fr) 2000-08-24
CA2342219A1 (fr) 2000-03-16
PT1114206E (pt) 2003-07-31
ES2193728T3 (es) 2003-11-01
JP4263363B2 (ja) 2009-05-13
ATE233329T1 (de) 2003-03-15
WO2000014305A1 (fr) 2000-03-16
CA2342219C (fr) 2008-09-23
EP1114206B1 (fr) 2003-02-26
US6652728B1 (en) 2003-11-25

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