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
  • C25D3/38—Electroplating: Baths therefor from solutions 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
  • C25D5/00—Electroplating characterised by the process; Pretreatment or after-treatment of workpieces
  • C25D5/18—Electroplating using modulated, pulsed or reversing current
• • C—CHEMISTRY; METALLURGY
  • C25—ELECTROLYTIC OR ELECTROPHORETIC PROCESSES; APPARATUS THEREFOR
  • C25D—PROCESSES FOR THE ELECTROLYTIC OR ELECTROPHORETIC PRODUCTION OF COATINGS; ELECTROFORMING; APPARATUS THEREFOR
  • C25D5/00—Electroplating characterised by the process; Pretreatment or after-treatment of workpieces
  • C25D5/60—Electroplating characterised by the structure or texture of the layers
  • C25D5/605—Surface topography of the layers, e.g. rough, dendritic or nodular layers
  • C25D5/611—Smooth layers
• • C—CHEMISTRY; METALLURGY
  • C25—ELECTROLYTIC OR ELECTROPHORETIC PROCESSES; APPARATUS THEREFOR
  • C25D—PROCESSES FOR THE ELECTROLYTIC OR ELECTROPHORETIC PRODUCTION OF COATINGS; ELECTROFORMING; APPARATUS THEREFOR
  • C25D5/00—Electroplating characterised by the process; Pretreatment or after-treatment of workpieces
  • C25D5/627—Electroplating characterised by the visual appearance of the layers, e.g. colour, brightness or mat appearance

Definitions

• This invention relates to the use of pulse reverse plating to deposit copper from acid solutions onto decorative substrates, to produce a more even distribution of the copper deposit.
• One of these applications is plating aluminium alloy automobile wheels, whereby the aluminium alloy surface is cleaned and degreased prior to immersion in a zincate solution, which leaves a thin zinc coating on the alloy surface. Because of the acidic nature of the copper plating solution, the zincate film would be destroyed upon immersion. To avoid destruction of the zincate film, a thin nickel coating is normally electrodeposited from a mildly acidic bath onto the zincate film, and then copper is subsequently deposited onto the nickel by electroplating from the highly acidic copper solution. The zincate/nickel treatment facilitates the plating of the copper onto aluminium alloy substrates, which cannot be electroplated directly. In the specific example of aluminium alloy automobile wheels, it is common practice to deposit a relatively thick copper film, which is usually subjected to a polishing operation prior to electrodeposition of the final nickel and chromium finish.
• the deposition of copper serves two purposes: (1) it can have levelling properties and thus can be used to hide blemishes in the cast aluminium wheel, and (2) it is soft and easily polished. Polishing of the copper surface leaves a smooth finish that looks attractive when the final finish is applied. In addition, polishing the surface spreads the soft copper and effectively seals any pores in the copper deposit, thus improving the corrosion resistance of the deposit.
• One of the drawbacks of the current technique is that a minimum thickness of copper must be deposited onto the aluminium base to ensure that no areas of the copper deposit are removed completely during the polishing operation, and to provide adequate protection of the aluminium during subsequent processing stages.
• the distribution of the copper plate is generally uneven. To achieve the required minimum thickness in recesses, excess copper is plated onto the more exposed areas of the wheel, which is very wasteful and costly for the plater.
• Another application for copper deposition is electroplating onto plastic substrates, which is very common in the automotive industry.
• the plastic substrate is pre-treated to allow it to accept a thin nickel deposit that is deposited by electroless means.
• a substantial layer of copper is applied before the final finish of nickel and chromium is applied.
• a minimum copper thickness is normally specified by the end-user of the plated part, for example the automotive manufacturer. Due to the poor distribution of copper metal deposited from conventional decorative electrolytes, achieving this minimum copper thickness in the recesses of complex-shaped parts results in excessive amounts of copper deposited on the exposed areas.
• Treeing and burning are familiar terms well known to those skilled in the electroplating art and describe faults in the plated deposit that can occur on exposed areas of an electroplated article.
• the basic chemistry of the additives used for electronics applications, and their performance under pulse reverse current plating conditions as compared to direct current conditions is explained by T. Pearson, “Effect of Pulsed Current On The Electrodeposition of Chromium and Copper”, PhD thesis, Aston University, United Kingdom, 1989, the subject matter of which is herein incorporated by reference in it is entirety.
• the additives are broadly similar to those used in general rack plating applications, and broadly comprise a sulphopropyl sulphide and a polyalkylene glycol that operate in conjunction with chloride ion.
• the use of pulse reverse current with these additives results in an electrochemical effect that causes an improved metal distribution. It is this effect that is utilised to plate copper into the holes on circuit boards. These holes are typically 0.5 mm diameter and 2-3 mm deep. The effective current density in these holes is extremely low and outside of the normal range expected in a general rack plating applications such as plating of alloy wheels.
• plating bath compositions formulated for printed circuit board applications are generally very simple and do not provide a fully bright and levelled copper deposit. Conversely, in general rack plating applications, it is the appearance of the copper deposit that is of prime importance. Because pulse plating is not used, the effect of further levellers and brightening agents on this distribution effect is inconsequential.
• the base composition of the electrolyte used for electronics applications is also different from that used in a typical rack plating application.
• a plating bath used for electronic/circuit board applications will contain 75 g/l of copper sulphate pentahydrate, 115 ml/l of concentrated sulphuric acid, 40 mg/l of chloride ion, and proprietary additives (a “low-metal/high acid bath”).
• a bath used for general-purpose rack plating typically contains 220 g/l of copper sulphate pentahydrate, 35 ml/l of concentrated sulphuric acid, 80 mg/l of chloride ion and proprietary additives (a “high-metal/low acid” bath).
• the inventors have surprisingly found that the pulse reverse current plating techniques used for printed circuit boards can translate very well to the application of plating copper in general rack plating applications including the aforementioned aluminium alloy automobile wheels and plastic substrates. This is surprising in that the current density range is very different from that applied to printed circuit boards.
• the inventors have found that the use of pulse reverse current plating in general rack plating applications causes less waste of copper as compared to conventional baths in various applications where articles are plated to a minimum thickness.
• the copper plating stage may consist of a period of pulse reverse electrolysis followed by a period of direct current electrolysis to leave the final deposit brighter than if pulse reverse electrolysis only had been applied.
• the low current density regions of an article plated with pulse reverse electrolysis retain a bright appearance when suitable proprietary additives are used, thus leaving a bright appearance across the whole item.
• the use of the pulse reverse current technique is ideally suited to applications where a more even distribution of the copper deposit is desirable, for example when plating to a minimum thickness specification, such as for alloy wheels or when plating plastic parts for automotive use.
• pulse reverse plating to deposit copper can be used for a method of plating decorative articles in an acidic copper electroplating bath comprising the steps of:
• the acid copper-plating bath further comprises a polyether and a divalent sulphur compound.
• the present invention utilizes pulse-reverse current for plating decorative articles with copper in an acidic copper plating bath to produce a desired thickness of copper on the surfaces of the decorative articles.
• the present invention is particularly useful for plating a more uniform thickness of copper onto aluminium alloy wheels and plastic parts for automotive use.
• the acidic copper plating bath of the invention generally comprises copper ions, a source of counter ions, and chloride ions. Other additives may also be added to the bath to improve the copper deposit.
• Copper ions are present in the plating bath at a concentration of about 10 to 50 g/l.
• Copper sulphate pentahydrate is an example of a copper compound that is useful in the baths of the present invention, although other copper compounds would also be known to one skilled in the art.
• the plating bath generally comprises copper sulphate pentahydrate at a concentration of about 50 to 100 g/l, preferably about 75 g/l.
• the source of counter ions in the plating bath is generally sulphate ions or methanesulphonate/methanesulphonic acid.
• a preferred source of sulphate ions is sulphuric acid.
• the counter ion is present in the plating bath at a concentration of about 50-250 ml/l, preferably about 100-150 ml/l, and most preferably about 115 ml/l.
• Chloride ions are present in the plating bath at a concentration of about 10-500 mg/l, preferably about 50-150 mg/l.
• the plating bath of the present invention further comprises a polyether and a divalent sulphur compound.
• the polyether is generally present in the plating bath at a concentration of about 50-5,000 mg/l, preferably about 300 mg/l.
• the polyether generally has a molecular weight of between 500 and 100,000.
• Preferred polyethers include polyethylene glycol and an ethylene oxide/propylene oxide co-polymer.
• the divalent sulphur compound is generally present in the plating bath at a concentration of about 1-150 mg/l, preferably about 30-50 mg/l.
• Preferred divalent sulphur compounds include mercatopropanesulponic acid or an alkali metal salt thereof, bis-(propane-3-sulphonic acid)disulphide or an alkali metal salt thereof, and bis-(ethane-2-sulphuric acid)disulphide or an alkali metal salt thereof.
• levelling compounds and brighteners may also be added to the plating bath compositions of the instant invention.
• the brighteners and levellers are added to enhance the visual performance of the deposit produced from the plating bath.
• the pulse plating regime of the plating bath consists of alternating cathodic and anodic pulses.
• the cathodic pulse time is generally between 5 and 100 ms, and the anodic pulse time is generally between 0.1 and 10 ms.
• the plating regime may comprise a final cathodic period of extended time, up to about 1 hour.
• the average applied current density is generally between 0.5-5.0 A/dm 2 .
• the current density during the anodic pulse is typically between 1 and 5 times the current density during the cathodic pulse.
• the Hull cell tests were done with a steel panel in order for the copper deposit thickness to be measured by X-ray fluorescence (XRF) technique.
• XRF X-ray fluorescence
• the panels were first plated with a minimal thickness of copper (approximately 0.1-0.2 ⁇ m) from a cyanide copper solution before being transferred to the Hull cell. All Hull cell tests were carried out at 25° C. using a “sulfast” copper anode.
• the pulse current regime was 10 ms cathodic, 0.5 ms anodic, which is a normal pulse regime for printed circuit board applications.
• Examples 1-5 are illustrative of the prior art and represent the current technology for general acid copper plating.
• the compositions and plating conditions used in these examples are set forth below in Table 1.
• TABLE 1 Prior art acid copper plating conditions Example 1
• Example 2 Example 3
• Example 4 Example 5
• Additive 30 mg/l disodium salt 2 Type of plating Direct current Pulse reverse Direct current Pulse reverse Direct current Current 1 amp 1 amp 1 amp 1 amp Plat
• a solution was prepared containing 210 ⁇ l copper sulphate pentahydrate, 32 ml/l sulphuric acid and 85 mg/l of chloride ion.
• Proprietary additives (Cumac 8000SL, a MacDermid process for general rack acid copper plating) were added.
• a Hull cell panel was plated at 1 amp for 15 minutes with direct current. The thickness was measured at points on the panel corresponding to primary current densities of 2.0 A/dm 2 and 0.1 A/dm 2 . The thickness at 2.0 A/dm 2 was divided by the thickness at 0.1 A/dm 2 to give a thickness ratio 6.07:1. The panel appearance was bright across the whole range.
• a solution was prepared as in example 1 and a Hull cell panel was plated for 15 minutes using a pulse reverse current regime with an average current of 1 amp and an anodic:cathodic current density of approximately 3:1. The thickness ratio was calculated as before and was 6.8:1. The panel appearance was smooth matte in high current density areas and bright in low current density areas.
• a solution was prepared containing 75 g/l of copper sulphate pentahydrate, 115 ml/l of sulphuric acid, 85 mg/l of chloride ion and Cumac 8000SL additives.
• a Hull cell panel was plated at 1 amp for 15 minutes using direct current and the thickness ratio was calculated as 4.0:1. The deposit was fully bright across the whole panel.
• a solution was prepared as in example 3 and a Hull cell panel was plated for 15 minutes using a pulse reverse current regime with an average current of 1 amp and an anodic:cathodic current density of approximately 2:1. The thickness ratio was calculated as before and was 3.0:1. The deposit was smooth matte in high current density areas and bright in low current density areas.
• a solution was prepared containing 75 g/l of copper sulphate pentahydrate, 115 ml/l of sulphuric acid and 75 mg/l of chloride ion. 300 mg/l of a polyalkyleneglycol and 30 mg/l of bis-(ethane-2-sulphate)disulphide disodium salt was added. A Hull cell panel was plated at 1 amp for 15 minutes using direct current and the thickness ratio was calculated as 4.0:1. The deposit was semi-bright across the whole range.
• Examples 6-12 illustrate non-limiting plating baths of the instant invention.
• the compositions and plating conditions used in these examples are set forth below in Tables 2-3. TABLE 2 Various copper plating baths of the instant invention
• Example 6 Example 7
• Example 8 Example 9 Copper sulphate 75 g/l 75 g/l 75 g/l 75 g/l pentahydrate Sulfuric acid 115 ml/l 115 ml/l 115 ml/l 115 ml/l Chloride ion 75 mg/l 75 mg/l 150 mg/l 150 mg/l Additive 300 mg/l PAG 1 MacuSpec PPR 300 mg/l PAG 300 mg/l PAG Additive 30 mg/l disodium salt 2 30 mg/l disodium salt 3 50 mg/l disodium salt 3 Type of plating Pulse reverse Pulse reverse Pulse reverse Pulse reverse Current 1 amp 1 amp 1 amp 1 amp Plating time 15 minutes 15 minutes 15 minutes 15 minutes Thickness ratio 2.20:1
• Example 10 Copper sulphate 75 g/l 75 g/l 75 g/l pentahydrate Sulfuric acid 115 ml/l 115 ml/l 115 ml/l Chloride ion 75 mg/l 75 mg/l 75 mg/l Additive 300 mg/l PAG 1 300 mg/l PAG 300 mg/l PAG Additive 30 mg/l disodium salt 2 30 mg/l disodium salt 3 30 mg/l disodium salt 3 Additive 40 mg/l levelling compound A 50 mg/l levelling compound B 40 mg/l levelling compound A Type of plating Pulse reverse Pulse reverse Pulse reverse Current 1 amp 1 amp 1 amp Plating time 15 minutes 15 minutes 15 minutes Thickness ratio 1.70:1 2.20:1 2.15:1
• a solution was prepared containing 75 g/l of copper sulphate pentahydrate, 115 ml/l of sulphuric acid and 75 mg/l of chloride ion. 300 mg/l of a polyalkyleneglycol and 30 mg/l of bis-(ethane-2-sulphate)disulphide disodium salt was added.
• a Hull cell panel was plated for 15 minutes using a pulse reverse current regime with an average current of 1 amp and an anodic:cathodic current density of approximately 2:1. The thickness ratio was calculated as 2.20:1. The panel was smooth matte in high current density areas and semi-bright in low current density areas.
• a solution was prepared containing 75 g/l copper sulphate pentahydrate, 115 ml/l sulphuric acid and 75 mg/l of chloride ion.
• Proprietary additives MacuSpec PPR, a MacDermid process for plating of printed circuit boards
• Hull cell panel was plated for 15 minutes using a pulse reverse current regime with an average current of 1 amp and an anodic:cathodic current density of approximately 2:1.
• the thickness ratio was calculated as 1.9:1.
• the deposit was smooth matte in high current density areas and semi-bright in low current density areas.
• a solution was prepared containing 75 g/l copper sulphate pentahydrate, 115 ml/l sulphuric acid and 150 mg/l of chloride ion. 300 mg/l of polyalkyleneglycol and 30 mg/l of bis-(3-sulphopropyl)disulphide disodium salt were added.
• a Hull cell panel was plated for 15 minutes using a pulse reverse current regime with an average current of 1 amp and an anodic:cathodic current density of approximately 2:1. The thickness ratio was calculated as 2.20:1. The deposit was smooth matte in high current density areas and semi-bright in low current density areas.
• a solution was prepared containing 75 g/l copper sulphate pentahydrate, 115 ml/l sulphuric acid and 150 mg/l of chloride ion. 300 mg/l of polyalkyleneglycol and 50 mg/l of bis-(3-sulphopropyl)disulphide disodium salt were added.
• a Hull cell panel was plated for 15 minutes using a pulse reverse current regime with an average current of 1 amp and an anodic:cathodic current density of approximately 2:1. The thickness ratio was calculated as 2.15:1. The deposit was smooth matte in high current density areas and semi-bright in low current density areas.
• a solution was prepared containing 75 g/l copper sulphate pentahydrate, 115 ml/l sulphuric acid and 75 mg/l of chloride ion. 300 mg/l of polyalkyleneglycol, 30 mg/l of bis-(ethane-2-sulphate)disulphide disodium salt and 40 mg/l of commercially available levelling compound A were added.
• a Hull cell panel was plated for 15 minutes using a pulse reverse current regime with an average current of 1 amp and an anodic:cathodic current density of approximately 2:1. The thickness ratio was calculated as 1.70:1. The deposit was smooth matte in high current density areas and fully bright in low current density areas.
• a solution was prepared containing 75 g/l copper sulphate pentahydrate, 115 ml/l sulphuric acid and 75 mg/l of chloride ion. 300 mg/l of polyalkyleneglycol, 30 mg/l of bis-(3-sulphopropyl)disulphide disodium salt and 50 mg/l of commercially available levelling compound B were added.
• a Hull cell panel was plated for 15 minutes using a pulse reverse current regime with an average current of 1 amp and an anodic:cathodic current density of approximately 2:1. The thickness ratio was calculated as 2.20:1. The deposit was smooth matte in high current density areas and fully bright in low current density areas.
• a solution was prepared containing 75 g/l copper sulphate pentahydrate, 115 ml/l sulphuric acid and 75 mg/l of chloride ion. 300 mg/l of polyalkyleneglycol, 30 mg/l of bis-(3-sulphopropyl)disulphide disodium salt and 40 mg/l of commercially available levelling compound A were added.
• a Hull cell panel was plated for 15 minutes using a pulse reverse current regime with an average current of 1 amp and an anodic:cathodic current density of approximately 2:1, followed by 1 amp for 5 minutes of direct current. The thickness ratio was calculated as 2.15:1. The deposit was bright across the entire panel.

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• 2002
  • 2002-10-21 US US10/274,634 patent/US20040074775A1/en not_active Abandoned
• 2003
  • 2003-08-06 WO PCT/US2003/024498 patent/WO2004038070A2/fr not_active Ceased
  • 2003-08-06 AU AU2003265370A patent/AU2003265370A1/en not_active Abandoned
  • 2003-08-20 TW TW092122858A patent/TWI261075B/zh not_active IP Right Cessation

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