CA2193559C - Substrate with protective coating thereon - Google Patents
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- CA2193559C CA2193559C CA 2193559 CA2193559A CA2193559C CA 2193559 C CA2193559 C CA 2193559C CA 2193559 CA2193559 CA 2193559 CA 2193559 A CA2193559 A CA 2193559A CA 2193559 C CA2193559 C CA 2193559C
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Abstract
An article is coated with a multilayer coating comprising a nickel layer deposited on the surface of the article, a palladium layer deposited on the nickel layer, a ruthenium layer deposited on the palladium layer, a refractory metal, preferably zirconium, layer deposited on the ruthenium layer, and a refractory metal compound, preferably zirconium nitride, deposited on the refractory metal layer. The coating provides the color of polished brass to the article and also provides abrasion and corrosion protection.
Description
2193~~9 SUBSTRATE WITH PROTECTIVE
COATING THEREON
Field of the Invention The instant invention relates to metallic substrates such as brass coated with a protective multilayer metallic coating.
Background of the Invention It is currently the practice with various brass articles such as lamps, trivets, candlesticks, door knobs and handles and the like to first buff and polish the surface of the article to a high gloss and to then apply a protective organic coating, such as one comprised of acrylics, urethanes, epoxies, and the like, onto this polished surface. While this system is generally quite satisfactory it has the drawback that the buffing and polishing operation, particularly if the article is of a complex shape, is labor intensive. Also, the known organic coatings are not always as durable as desired, particularly in outdoor applications where the articles they are exposed to the elements and ultraviolet radiation. It would, therefore, be quite advantageous if brass articles, or indeed other metallic articles, could be provided with a coating which gave the article the appearance of highly polished brass and also provided wear resistance and corrosion protection.
The present invention provides such a coating.
Summary of the Invention The present invention is directed to a metallic substrate having a multi-layer coating disposed or deposited on its surface.
More particularly, it is directed to a metallic substrate, particularly brass, having deposited on its surface multiple 2193J~9 superposed metallic layers of certain specific types of metals or metal compounds. The coating is decorative and also provides corrosion and wear resistance. The coating simulates the appearance of highly polished brass, i.e. has a brass color tone.
Thus, an article surface having the coating thereon simulates a highly polished brass surface.
This invention relates to an article comprising a metallic substrate having disposed on at least a portion of its surface a multi-layer coating simulating brass comprising: at least one layer comprised of nickel over at least a portion of said surface of said substrate; a layer comprised of palladium over at least a portion of said layer comprised of nickel; a layer comprised of ruthenium over at least a portion of said layer comprised of palladium; a layer comprised of zirconium or titanium over at least a portion of said layer comprised of ruthenium; and a layer comprised of zirconium compound or titanium compound over at least a portion of said layer comprised of zirconium or titanium.
This invention also relates to an article comprising a subst rate having on at least a port ion of its surface a coat ing simulating brass which comprises a first layer comprised of nickel;
a second layer on at least a portion of said second layer comprised of palladium; a third layer on at least a portion of said second layer comprised of ruthenium; a fourth layer on at least a portion of said third layer comprised of zirconium or titanium; and a fifth layer on at least a portion of said fourth layer comprised of a 219~J~~9 zirconium compound or titanium compound.
A first layer deposited directly on the surface of the substrate is comprised of nickel. Disposed over the nickel layer is a layer comprised of palladium. This palladium layer is thinner than the nickel layer. Over the palladium layer is a layer comprised of ruthenium. Over the ruthenium layer is a layer comprised of a non-precious refractory metal such as zirconium, t itanium, hafnium or tantalum, preferably zirconium or t itanium. A
top layer comprised of a zirconium compound, titanium compound, hafnium compound or tantalum compound, preferably a titanium compound or a zirconium compound such as zirconium nitride or titanium nitride, is disposed over the refractory metal layer, preferably zirconium layer.
The nickel, palladium and ruthenium layers are applied by electroplating. The refractory metal layer such as zirconium layer and refractory metal compound layer such as zirconium compound layer are applied by vapor deposition such as sputter ion deposition.
Brief Description of the Drawings FIG. 1 is a cross-sectional view of a portion of the substrate having the multi-layer coating deposited on its surface.
2a Description of the Preferred Embodiment The substrate 12 can be any metal or metallic alloy substrate such as copper, steel, brass, tungsten, nickel alloys, and the like. In a preferred embodiment the substrate is brass.
The nickel layer 13 is deposited on the surface of the substrate 12 by conventional and well known plating processes.
These processes include electroplating processes using conventional and well known electroplating baths such as, for example, a Watts bath as the plating solution. Typically such baths contain nickel sulfate, nickel chloride, and boric acid dissolved in water. All chloride, sulfamate and fluoroborate plating solutions can also be used. These baths can optionally include a number of well known and conventionally used compounds such as leveling agents, brighteners, and the like. To produce specularly bright nickel layer at least one brightener from class I and at least one brightener from class II is added to the plating solution. Class I brighteners are organic compounds which contain sulfur. Class II brighteners are organic compounds which do not contain sulfur. Class II brighteners can also cause leveling and, when added to the plating bath without the sulfur-containing class I brighteners, result in semi-bright nickel deposits. These class I brighteners include alkyl naphthalene and benzene sulfonic acids, the benzene and naphthalene di- and trisulfonic acids, benzene and naphthalene sulfonamides, and sulfonamides such as saccharin, vinyl and allyl sulfonamides and sulfonic acids. The class II
brighteners generally are unsaturated organic materials such as, for example, acetylenic or ethylenic alcohols, ethoxylated and propoxylated acetylenic alcohols, coumarins, and aldehydes. These Class I and Class II brighteners are well known to those skilled in the art and are readily commercially available. They are described, inter alia, in U.S. Patent No. 4,421,611.
The nickel layer is preferably comprised of semi-bright nickel or bright nickel, more preferably bright nickel. The thickness~of the nickel layer is a thickness which is effective to provide improved corrosion protection to the underlying substrate.
Generally this average thickness is from at least about 100 millionths (0.0001) of an inch, preferably at least about 150 millionths (0.00015) of an inch, and more preferably at least about 200 millionths (0.0002) of an inch. The upper thickness limit is generally not critical and is governed by secondary considerations such as cost, appearance, and the like. Generally, however, an average thickness of about 3,500 millionths (0.0035), preferably about 3,000 millionths of an inch, and more preferably about 2,500 millionths (0.0025) of an inch should not be exceeded.
As is well known in the art before the nickel layer is deposited on the substrate the substrate is subjected to said activation by being placed in a conventional and well known acid bath.
In a more preferred embodiment the nickel layer 13 is comprised of~two different nickel layers 14 and 16. Layer 14 is comprised of bright nickel. The bright plate 13 is deposited by conventional electroplating processes directly on the surface of substrate 12.
Disposed on the nickel, preferably bright nickel layer 13 is a relatively thin layer comprised of palladium. The palladium strike layer 18 may be deposited on the nickel layer 13 by conventional and well known palladium electroplating techniques.
Thus for example, the anode can be an inert platinized titanium while the cathode is the substrate 12 having the nickel layer 13 thereon. The palladium is present in the bath as a palladium salt or complex ion. Some of the complexing agents include polyamines such as described in U.S. patent Nv. 4,486,274.
Some other palladium complexes such as palladium tetra-amine complex used as the source of palladium in a number of palladium electroplating processes are described in U.S. patent Nos. 4,622,110; 4,552,628; and 4,628,165, Same palladium electroplating processes are described in U.S. patent Nos. 4,487,665; 4,491,507 and 4,545,869.
The palladium layer 18 generally has an average thickness of at least about 0.25 millionths (0.00000025) of an inch, preferably at least about 0.5 millionths (0.0000005) of an inch, and more preferably at least about one millionth (0.000001) of an inch.
Generally, the upper range of thickness is not critical and is determined by secondary considerations such as cost. However, the thickness of~the palladium strike layer should generally not exceed about 50 millionths (0.00005) of an inch, preferably 15 millionths (0.000015) of an inch,'and more preferably 10 millionths (0.000010) of an inch.
The ruthenium layer 20 is deposited on the palladium layer 18 in a variety of conventional and well known ways such as for example by plating, sputtering, vacuum deposition, and depositing the ruthenium metal as a finely divided dispersion in an organic vehicle. The ruthenium is preferably deposited by plating, preferably electroplating.
The ruthenium electroplating processes and plating baths are conventional and well known. They are described, for example, in the Journal of the Chemical Society of London, 1971 edition, page 839, by C.D. Burke and J.O. 0'Meardi and Electrodeposition of Alloys, Vol. II, pp. 4-29, Abner Brenner (1963). The Ruthenium electroplating baths may be acidic or nonacidic. Some illustrative examples of nonacidic ruthenium electroplating baths are described in U.S. Patent Nos. 4,297,178 and 4,507,183.
Some illustrative examples of acid ruthenium plating baths are described in U.S. Patent No.
3,793,162. Some other ruthenium plating baths are disclosed in U.S. Patent Nos.-3,576,724 and 4,377,448. The ruthenium plating baths includes the nitrous salt baths and the sulfamate baths.
The ruthenium may be electroplated by use of continuous direct current densities or by use of pulse current plating, i.e., where a current is generated for a first time period and is absent during a second time period, the first .and second time period reoccur cyclically. Pulse current plating of ruthenium is described, for example, in U.S. Patent No. 4,082,622, The average thickness of the ruthenium layer 20 is at least about 2 millionths (0.000002) of an inch, preferably at least about millionths (0.000005) of an inch, and more preferably at leas t about 8 millionths (0.000008) of an inch. The upper thickness range is not critical and is generally dependent on economic considerations. Generally, an average thickness of about 100 millionths (0.0001) of an inch, preferably about 75 millionths (0.000075), and more preferably about 50 millionths (0.00005) of an inch should not be exceeded.
Disposed over the ruthenium layer 20 is a layer 22 comprised of a non-precious refractory metal such as hafnium, tantalum, zirconium or titanium, preferably zirconium or titanium, and more preferably zirconium.
Layer 20 serves, inter alia, to improve or enhance the adhesion of layer 24 to layer 20. Layer 22 is deposited on the ruthenium layer 20 by conventional and well known techniques such as vacuum coating, physical vapor deposition such as ion sputtering, and the like. Ion sputtering techniques and equipment are disclosed, inter alia, in T. Van Vorous, "Planar Magnetron Sputtering; A New Industrial Coating Technique", Solid State Technology " Dec. 1976, pp 62-66; U. Kapacz and S. Schulz, "Industrial Application of Decorative Coatings - Principle and Advantages of the Sputter Ion Plating Process", Soc. Vac. Coat., Proc. 34th Ara. Techn. Conf., Philadelphia, U.S.A., 1991, 48-61;
and U.S. patent Nos. 4,162,954, and 4,591,418, Briefly, in the sputter ion deposition process the refractory metal such as titanium or zirconium target, which is the cathode, and the substrate are placed in a vacuum chamber. The air in the chamber is evacuated to produce vacuum conditions in the chamber.
An inert gas, such as Argon, is introduced into the chamber. The gas particles are ionized and are accelerated to the target to dislodge titanium or zirconium atoms. The dislodged target material is then typically deposited as a coating film on the substrate.
Layer 22 has a thickness which is at least effective to improve the adhesion of layer 24 to layer 20. Generally, this thickness is at Ieast about 0.25 millionths (0.00000025) of an inch, preferably at least about 0.5 millionths (0.0000005) of an inch, and more preferably at least about one millionth (0.000001) of an inch. The upper thickness range is not critical and is generally dependent upon considerations such as cost. Generally, however, layer 22 should not be thicker than about 50 millionths (0.00005) of an inch, preferably about 15 millionths (0.000015) of an inch, and more preferably about 10 millionths (0.000010) of an inch.
? ~ ~3~~~
In a preferred embodiment of the present invention layer 22 is comprised of titanium or zirconium, preferably zirconium, and is deposited by sputter ion plating.
Layer 24 is comprised of a hafnium compound, a tantalum compound, a titanium compound or a zirconium compound, preferably a titanium compound or a zirconium compound, and more preferably a zirconium compound. The titanium compound is selected from titanium nitride, titanium carbide, and titanium carbonitride, with titanium nitride being preferred. The zirconium compound is selected from zirconium nitride, zirconium carbonitride, and zirconium carbide, with zirconium nitride being preferred.
Layer 24 provides wear and abrasion resistance and the desired color or appearance, such as for example, of polished brass. Layer 24 is deposited on layer 22 by any of the well known and conventional plating or deposition processes such as vacuum coating, reactive sputter ion plating, and the like. The preferred method is reactive ion sputter plating.
Reactive ion sputter is generally similar to ion sputter deposition except that a reactive gas which reacts with the dislodged target material is introduced into the chamber. Thus, in the case where zirconium nitride is the top layer 24, the target is comprised of zirconium and nitrogen gas is the reactive gas introduced into the chamber. By controlling the amount of nitrogen available to react with the zirconium, the color of the zirconium nitride can be made to be similar to that of brass of various hues.
Layer 24 has a thickness at least effective to provide abrasion resistance. Generally, this thickness is at least 2 millionths (0.000002) of an inch, preferably at least 4 millionths (0.000004) of an inch, and more preferably at least 6 millionths (0.000006) of an inch. The upper thickness range is generally not critical and is dependent upon considerations such as cost.
Generally a thickness of about 30 millionths (0.00003) of an inch, preferably about 25 millionths (0.000025) of an inch, and more preferably about 20 millionths (0.000020) of an inch should not be exceeded.
Zirconium nitride is the preferred coating material as it most closely provides the appearance of polished brass.
In order that the invention may be more readily understood the following example is provided. The example is illustrative and does not limit the invention thereto.
Brass door escutcheons are placed in a conventional soak cleaner bath containing the standard and well known soaps, detergents, defloculants and the like which is maintained at a pH
of 8.9 - 9.2 and a temperature of 180 - 200oF for 30 minutes. The brass escutcheons are then placed for six minutes in-a conventional ultrasonic alkaline cleaner bath. The ultrasonic cleaner bath has a pH of 8.9 - 9.2, is maintained at a temperature of about 160 -180oF, and contains the conventional and well known soaps, detergents, defloculants and the like. After the ultrasonic cleaning the escutcheons are rinsed and placed in a conventional ~v 2 ~ 9 3 X59 alkaline electro cleaner bath for about two minutes. The electro cleaner bath contains an insoluble submerged steel anode, is maintained at a temperature of about 140 - 180oF, a pH of about 10.5 - 11.5, and contains standard and conventional detergents.
The escutcheons are then rinsed twice and placed in a conventional acid activator bath for about one minute. The acid activator bath has a pH of about 2.0 - 3.0, is at an ambient temperature, and contains a sodium fluoride based acid salt. The escutcheons are then rinsed twice and placed in a bright nickel plating bath for about 24 minutes. The bright nickel bath is generally a conventional bath which is maintained at a temperature of about 130 - 150oF, a pH of about 4.0 - 4.8, contains NiS04, NiCLz, boric acid, and brighteners. A bright nickel layer of an average thickness of about 750 millionths (0.00075) of an inch is deposited on the semi-bright nickel layer. The bright nickel plated escutcheons are rinsed three times and placed for about one and a half minutes in a conventional palladium plating bath. The palladium bath utilizes an insoluble platinized niobium anode, is maintained at a temperature of about 95 - 140oF, a pH of about 3.7 - 4.5, contains from about 1-5 grams per liter of palladium (as metal), and about 50-100 grams per liter of sodium chloride. A palladium layer of an average thickness of about three millionths (0.000003) of an inch is deposited on the bright nickel layer. The palladium plated escutcheons are then rinsed twice.
2 ~ ~3~59 The palladium plated escutcheons are then placed into a conventional ruthenium plating bath for about ten minutes. The ruthenium bath utilizes insoluble platinized titanium anodes, is maintained at a temperature of about 150-170 deg F, a pH of about 1.0-2.0, and contains about 3 grams per liter of ruthenium. A
ruthenium layer of an average thickness of about 10 millionths of an inch is deposited over the palladium layer. The escutcheons are then thoroughly rinsed and dried.
The ruthenium plated escutcheons are placed ir1 a sputter ion plating vessel. This vessel is a stainless steel vacuum vessel marketed by Leybold A.G. of Germany. The vessel is generally a cylindrical enclosure containing a vacuum chamber which is adapted to be evacuated by means of pumps. A source of argon gas is connected to the chamber by an adjustable valve for varying the rate of flow of argon into the chamber. In addition, two sources of nitrogen gas are connected to the chamber by an adjustable valve for varying the rate of flow of nitrogen into the chamber.
Two pairs of magnetron-type target assemblies are mounted in a spaced apart relationship in the chamber and connected to negative outputs of variable D.C. power supplies. ~ The targets constitute cathodes and the chamber wall is an anode common to the target cathodes. The target material comprises zirconium.
A substrate carrier which carries the substrates, i.e., escutcheons, is provided, e.g., it may be suspended from the top of the chamber, and is rotated by a variable speed motor to carry the substrates between each pair of magnetron target assemblies. The 219~~~9 carrier is conductive and is electrically connected to the negative output of a variable D.C. power supply.
The ruthenium plated escutcheons are mounted onto the substrate carrier in the sputter ion plating vessel. The vacuum chamber is evacuated to a pressure of about 5x10'3 millibar and is heated to about 400oC via a radiative electric resistance heater.
The target material is sputter cleaned to remove contaminants from its surface. Sputter cleaning is carried out for about one half minute by applying power to the cathodes sufficient to achieve a current flow of about 18 amps and introducing argon gas at the rate of about 200 standard cubic centimeters per minute. A pressure of about 3x10'3 millibars is maintained during sputter cleaning.
The escutcheons are then cleaned by a low pressure etch process. The low pressure etch process is carried on for about five minutes and involves applying a negative D.C. potential which increases over a one minute period from about 1200 to about 1400 volts to the escutcheons and applying D.C. power to the cathodes to achieve a current flow of about 3.6 amps. Argon gas is introduced at a rate which increases over a one minute period from about 800 to about 1000 standard cubic centimeters per minute, and the pressure is maintained at about 1.1x10' millibars. The escutcheons are rotated between the magnetron target assemblies at a rate of one revolution per minute. The escutcheons are then subjected to a high pressure etch cleaning process for about 15 minutes. In the high pressure etch process argon gas is introduced into the vacuum chamber at a rate which increases over a 10 minute period from ~? 9359 about 500 to 650 standard cubic centimeters per minute (i.e., at the beginning the flow rate is 500 sccm and after ten minutes the flow rate is 650 sccm and remains 650 sccm during the remainder of the high pressure etch process), the pressure is maintained at about 2x10'1 millibars, and a negative potential which increases over a ten minute period from about 1400 to 2000 volts is applied to the escutcheons. The escutcheons are rotated between the magnetron target assemblies at about one revolution per minute.
The pressure in the vessel is maintained at about 2x10'1 millibar.
The escutcheons are then subjected to another low pressure etch cleaning process for about five minutes. During this low pressure etch cleaning process a negative potential of about 1400 volts is applied to the escutcheons, D.C. power is applied to the cathodes to achieve a current flow of about 2.6 amps, and argon gas is introduced into the vacuum chamber at a rate which increases over a five minute period from about 800 sccm (standard cubic centimeters per minute) to about 1000 sccm. The pressure is maintained at about 1.1x10'2 millibar and the escutcheons are rotated at about one rpm.
The target material is again sputter cleaned for about one minute by applying power to the cathodes sufficient to achieve a current flow of about 18 amps, introducing argon gas at a rate of about 150 sccm, and maintaining a pressure of about 3x10'3 millibars.
21.93559 During the cleaning process shields are interposed between the escutcheons and the magnetron target assemblies to prevent deposition of the target material onto the escutcheons.
The shields are removed and a layer of zirconium having an average thickness of about 3 millionths (0.000003) of an inch is deposited on the ruthenium layer of the escutcheons during a four minute period. This sputter deposition process comprises applying D.C. power to the cathodes to achieve a current flow of about 18 amps, introducing argon gas into the vessel at about 450 sccm, maintaining the pressure in the vessel at about 6x10'3 millibar, and rotating the escutcheons at about 0.7 revolutions per minute.
After the zirconium layer is deposited a zirconium nitride layer having an average thickness of about 14 millionths (0.000014) of an inch is deposited on the zirconium layer by reactive ion sputtering over a 14 minute period. A negative potential of about 200 volts D.C. is applied to the escutcheons while D.C. power is applied to the cathodes to achieve a current flow of about 18 amps.
Argon gas is introduced at a flow rate of about 500 sccm. Nitrogen gas is introduced into the vessel from two sources. One source introduces nitrogen at a generally steady flow rate of about 40 sccm. The other source is variable. The variable source is regulated so as to maintain a partial ion current of 6.3x10'11 amps, with the variable flow of nitrogen being increased or decreased as necessary to maintain the partial ion current at this predetermined value.
~193~5~
The pressure in-the vessel is maintained at about 7.5x10'3 millibar.
The zirconium-nitride coated escutcheons are then subjected to low pressure cool down, where the heating is discontinued, pressure is increased from about 1.1x10'z millibar to about 2x10'1 millibar, and argon gas is introduced at a rate of 950 sccm.
Although the present invention has been ~ described in conjunction with a preferred embodiment, it is to be understood that modifications and variations may be resorted to without departing from the spirit and scope of the invention as those skilled in the art will readily understand. Such modifications and variations are considered to be within the purview and scope of the invention and appended claims.
COATING THEREON
Field of the Invention The instant invention relates to metallic substrates such as brass coated with a protective multilayer metallic coating.
Background of the Invention It is currently the practice with various brass articles such as lamps, trivets, candlesticks, door knobs and handles and the like to first buff and polish the surface of the article to a high gloss and to then apply a protective organic coating, such as one comprised of acrylics, urethanes, epoxies, and the like, onto this polished surface. While this system is generally quite satisfactory it has the drawback that the buffing and polishing operation, particularly if the article is of a complex shape, is labor intensive. Also, the known organic coatings are not always as durable as desired, particularly in outdoor applications where the articles they are exposed to the elements and ultraviolet radiation. It would, therefore, be quite advantageous if brass articles, or indeed other metallic articles, could be provided with a coating which gave the article the appearance of highly polished brass and also provided wear resistance and corrosion protection.
The present invention provides such a coating.
Summary of the Invention The present invention is directed to a metallic substrate having a multi-layer coating disposed or deposited on its surface.
More particularly, it is directed to a metallic substrate, particularly brass, having deposited on its surface multiple 2193J~9 superposed metallic layers of certain specific types of metals or metal compounds. The coating is decorative and also provides corrosion and wear resistance. The coating simulates the appearance of highly polished brass, i.e. has a brass color tone.
Thus, an article surface having the coating thereon simulates a highly polished brass surface.
This invention relates to an article comprising a metallic substrate having disposed on at least a portion of its surface a multi-layer coating simulating brass comprising: at least one layer comprised of nickel over at least a portion of said surface of said substrate; a layer comprised of palladium over at least a portion of said layer comprised of nickel; a layer comprised of ruthenium over at least a portion of said layer comprised of palladium; a layer comprised of zirconium or titanium over at least a portion of said layer comprised of ruthenium; and a layer comprised of zirconium compound or titanium compound over at least a portion of said layer comprised of zirconium or titanium.
This invention also relates to an article comprising a subst rate having on at least a port ion of its surface a coat ing simulating brass which comprises a first layer comprised of nickel;
a second layer on at least a portion of said second layer comprised of palladium; a third layer on at least a portion of said second layer comprised of ruthenium; a fourth layer on at least a portion of said third layer comprised of zirconium or titanium; and a fifth layer on at least a portion of said fourth layer comprised of a 219~J~~9 zirconium compound or titanium compound.
A first layer deposited directly on the surface of the substrate is comprised of nickel. Disposed over the nickel layer is a layer comprised of palladium. This palladium layer is thinner than the nickel layer. Over the palladium layer is a layer comprised of ruthenium. Over the ruthenium layer is a layer comprised of a non-precious refractory metal such as zirconium, t itanium, hafnium or tantalum, preferably zirconium or t itanium. A
top layer comprised of a zirconium compound, titanium compound, hafnium compound or tantalum compound, preferably a titanium compound or a zirconium compound such as zirconium nitride or titanium nitride, is disposed over the refractory metal layer, preferably zirconium layer.
The nickel, palladium and ruthenium layers are applied by electroplating. The refractory metal layer such as zirconium layer and refractory metal compound layer such as zirconium compound layer are applied by vapor deposition such as sputter ion deposition.
Brief Description of the Drawings FIG. 1 is a cross-sectional view of a portion of the substrate having the multi-layer coating deposited on its surface.
2a Description of the Preferred Embodiment The substrate 12 can be any metal or metallic alloy substrate such as copper, steel, brass, tungsten, nickel alloys, and the like. In a preferred embodiment the substrate is brass.
The nickel layer 13 is deposited on the surface of the substrate 12 by conventional and well known plating processes.
These processes include electroplating processes using conventional and well known electroplating baths such as, for example, a Watts bath as the plating solution. Typically such baths contain nickel sulfate, nickel chloride, and boric acid dissolved in water. All chloride, sulfamate and fluoroborate plating solutions can also be used. These baths can optionally include a number of well known and conventionally used compounds such as leveling agents, brighteners, and the like. To produce specularly bright nickel layer at least one brightener from class I and at least one brightener from class II is added to the plating solution. Class I brighteners are organic compounds which contain sulfur. Class II brighteners are organic compounds which do not contain sulfur. Class II brighteners can also cause leveling and, when added to the plating bath without the sulfur-containing class I brighteners, result in semi-bright nickel deposits. These class I brighteners include alkyl naphthalene and benzene sulfonic acids, the benzene and naphthalene di- and trisulfonic acids, benzene and naphthalene sulfonamides, and sulfonamides such as saccharin, vinyl and allyl sulfonamides and sulfonic acids. The class II
brighteners generally are unsaturated organic materials such as, for example, acetylenic or ethylenic alcohols, ethoxylated and propoxylated acetylenic alcohols, coumarins, and aldehydes. These Class I and Class II brighteners are well known to those skilled in the art and are readily commercially available. They are described, inter alia, in U.S. Patent No. 4,421,611.
The nickel layer is preferably comprised of semi-bright nickel or bright nickel, more preferably bright nickel. The thickness~of the nickel layer is a thickness which is effective to provide improved corrosion protection to the underlying substrate.
Generally this average thickness is from at least about 100 millionths (0.0001) of an inch, preferably at least about 150 millionths (0.00015) of an inch, and more preferably at least about 200 millionths (0.0002) of an inch. The upper thickness limit is generally not critical and is governed by secondary considerations such as cost, appearance, and the like. Generally, however, an average thickness of about 3,500 millionths (0.0035), preferably about 3,000 millionths of an inch, and more preferably about 2,500 millionths (0.0025) of an inch should not be exceeded.
As is well known in the art before the nickel layer is deposited on the substrate the substrate is subjected to said activation by being placed in a conventional and well known acid bath.
In a more preferred embodiment the nickel layer 13 is comprised of~two different nickel layers 14 and 16. Layer 14 is comprised of bright nickel. The bright plate 13 is deposited by conventional electroplating processes directly on the surface of substrate 12.
Disposed on the nickel, preferably bright nickel layer 13 is a relatively thin layer comprised of palladium. The palladium strike layer 18 may be deposited on the nickel layer 13 by conventional and well known palladium electroplating techniques.
Thus for example, the anode can be an inert platinized titanium while the cathode is the substrate 12 having the nickel layer 13 thereon. The palladium is present in the bath as a palladium salt or complex ion. Some of the complexing agents include polyamines such as described in U.S. patent Nv. 4,486,274.
Some other palladium complexes such as palladium tetra-amine complex used as the source of palladium in a number of palladium electroplating processes are described in U.S. patent Nos. 4,622,110; 4,552,628; and 4,628,165, Same palladium electroplating processes are described in U.S. patent Nos. 4,487,665; 4,491,507 and 4,545,869.
The palladium layer 18 generally has an average thickness of at least about 0.25 millionths (0.00000025) of an inch, preferably at least about 0.5 millionths (0.0000005) of an inch, and more preferably at least about one millionth (0.000001) of an inch.
Generally, the upper range of thickness is not critical and is determined by secondary considerations such as cost. However, the thickness of~the palladium strike layer should generally not exceed about 50 millionths (0.00005) of an inch, preferably 15 millionths (0.000015) of an inch,'and more preferably 10 millionths (0.000010) of an inch.
The ruthenium layer 20 is deposited on the palladium layer 18 in a variety of conventional and well known ways such as for example by plating, sputtering, vacuum deposition, and depositing the ruthenium metal as a finely divided dispersion in an organic vehicle. The ruthenium is preferably deposited by plating, preferably electroplating.
The ruthenium electroplating processes and plating baths are conventional and well known. They are described, for example, in the Journal of the Chemical Society of London, 1971 edition, page 839, by C.D. Burke and J.O. 0'Meardi and Electrodeposition of Alloys, Vol. II, pp. 4-29, Abner Brenner (1963). The Ruthenium electroplating baths may be acidic or nonacidic. Some illustrative examples of nonacidic ruthenium electroplating baths are described in U.S. Patent Nos. 4,297,178 and 4,507,183.
Some illustrative examples of acid ruthenium plating baths are described in U.S. Patent No.
3,793,162. Some other ruthenium plating baths are disclosed in U.S. Patent Nos.-3,576,724 and 4,377,448. The ruthenium plating baths includes the nitrous salt baths and the sulfamate baths.
The ruthenium may be electroplated by use of continuous direct current densities or by use of pulse current plating, i.e., where a current is generated for a first time period and is absent during a second time period, the first .and second time period reoccur cyclically. Pulse current plating of ruthenium is described, for example, in U.S. Patent No. 4,082,622, The average thickness of the ruthenium layer 20 is at least about 2 millionths (0.000002) of an inch, preferably at least about millionths (0.000005) of an inch, and more preferably at leas t about 8 millionths (0.000008) of an inch. The upper thickness range is not critical and is generally dependent on economic considerations. Generally, an average thickness of about 100 millionths (0.0001) of an inch, preferably about 75 millionths (0.000075), and more preferably about 50 millionths (0.00005) of an inch should not be exceeded.
Disposed over the ruthenium layer 20 is a layer 22 comprised of a non-precious refractory metal such as hafnium, tantalum, zirconium or titanium, preferably zirconium or titanium, and more preferably zirconium.
Layer 20 serves, inter alia, to improve or enhance the adhesion of layer 24 to layer 20. Layer 22 is deposited on the ruthenium layer 20 by conventional and well known techniques such as vacuum coating, physical vapor deposition such as ion sputtering, and the like. Ion sputtering techniques and equipment are disclosed, inter alia, in T. Van Vorous, "Planar Magnetron Sputtering; A New Industrial Coating Technique", Solid State Technology " Dec. 1976, pp 62-66; U. Kapacz and S. Schulz, "Industrial Application of Decorative Coatings - Principle and Advantages of the Sputter Ion Plating Process", Soc. Vac. Coat., Proc. 34th Ara. Techn. Conf., Philadelphia, U.S.A., 1991, 48-61;
and U.S. patent Nos. 4,162,954, and 4,591,418, Briefly, in the sputter ion deposition process the refractory metal such as titanium or zirconium target, which is the cathode, and the substrate are placed in a vacuum chamber. The air in the chamber is evacuated to produce vacuum conditions in the chamber.
An inert gas, such as Argon, is introduced into the chamber. The gas particles are ionized and are accelerated to the target to dislodge titanium or zirconium atoms. The dislodged target material is then typically deposited as a coating film on the substrate.
Layer 22 has a thickness which is at least effective to improve the adhesion of layer 24 to layer 20. Generally, this thickness is at Ieast about 0.25 millionths (0.00000025) of an inch, preferably at least about 0.5 millionths (0.0000005) of an inch, and more preferably at least about one millionth (0.000001) of an inch. The upper thickness range is not critical and is generally dependent upon considerations such as cost. Generally, however, layer 22 should not be thicker than about 50 millionths (0.00005) of an inch, preferably about 15 millionths (0.000015) of an inch, and more preferably about 10 millionths (0.000010) of an inch.
? ~ ~3~~~
In a preferred embodiment of the present invention layer 22 is comprised of titanium or zirconium, preferably zirconium, and is deposited by sputter ion plating.
Layer 24 is comprised of a hafnium compound, a tantalum compound, a titanium compound or a zirconium compound, preferably a titanium compound or a zirconium compound, and more preferably a zirconium compound. The titanium compound is selected from titanium nitride, titanium carbide, and titanium carbonitride, with titanium nitride being preferred. The zirconium compound is selected from zirconium nitride, zirconium carbonitride, and zirconium carbide, with zirconium nitride being preferred.
Layer 24 provides wear and abrasion resistance and the desired color or appearance, such as for example, of polished brass. Layer 24 is deposited on layer 22 by any of the well known and conventional plating or deposition processes such as vacuum coating, reactive sputter ion plating, and the like. The preferred method is reactive ion sputter plating.
Reactive ion sputter is generally similar to ion sputter deposition except that a reactive gas which reacts with the dislodged target material is introduced into the chamber. Thus, in the case where zirconium nitride is the top layer 24, the target is comprised of zirconium and nitrogen gas is the reactive gas introduced into the chamber. By controlling the amount of nitrogen available to react with the zirconium, the color of the zirconium nitride can be made to be similar to that of brass of various hues.
Layer 24 has a thickness at least effective to provide abrasion resistance. Generally, this thickness is at least 2 millionths (0.000002) of an inch, preferably at least 4 millionths (0.000004) of an inch, and more preferably at least 6 millionths (0.000006) of an inch. The upper thickness range is generally not critical and is dependent upon considerations such as cost.
Generally a thickness of about 30 millionths (0.00003) of an inch, preferably about 25 millionths (0.000025) of an inch, and more preferably about 20 millionths (0.000020) of an inch should not be exceeded.
Zirconium nitride is the preferred coating material as it most closely provides the appearance of polished brass.
In order that the invention may be more readily understood the following example is provided. The example is illustrative and does not limit the invention thereto.
Brass door escutcheons are placed in a conventional soak cleaner bath containing the standard and well known soaps, detergents, defloculants and the like which is maintained at a pH
of 8.9 - 9.2 and a temperature of 180 - 200oF for 30 minutes. The brass escutcheons are then placed for six minutes in-a conventional ultrasonic alkaline cleaner bath. The ultrasonic cleaner bath has a pH of 8.9 - 9.2, is maintained at a temperature of about 160 -180oF, and contains the conventional and well known soaps, detergents, defloculants and the like. After the ultrasonic cleaning the escutcheons are rinsed and placed in a conventional ~v 2 ~ 9 3 X59 alkaline electro cleaner bath for about two minutes. The electro cleaner bath contains an insoluble submerged steel anode, is maintained at a temperature of about 140 - 180oF, a pH of about 10.5 - 11.5, and contains standard and conventional detergents.
The escutcheons are then rinsed twice and placed in a conventional acid activator bath for about one minute. The acid activator bath has a pH of about 2.0 - 3.0, is at an ambient temperature, and contains a sodium fluoride based acid salt. The escutcheons are then rinsed twice and placed in a bright nickel plating bath for about 24 minutes. The bright nickel bath is generally a conventional bath which is maintained at a temperature of about 130 - 150oF, a pH of about 4.0 - 4.8, contains NiS04, NiCLz, boric acid, and brighteners. A bright nickel layer of an average thickness of about 750 millionths (0.00075) of an inch is deposited on the semi-bright nickel layer. The bright nickel plated escutcheons are rinsed three times and placed for about one and a half minutes in a conventional palladium plating bath. The palladium bath utilizes an insoluble platinized niobium anode, is maintained at a temperature of about 95 - 140oF, a pH of about 3.7 - 4.5, contains from about 1-5 grams per liter of palladium (as metal), and about 50-100 grams per liter of sodium chloride. A palladium layer of an average thickness of about three millionths (0.000003) of an inch is deposited on the bright nickel layer. The palladium plated escutcheons are then rinsed twice.
2 ~ ~3~59 The palladium plated escutcheons are then placed into a conventional ruthenium plating bath for about ten minutes. The ruthenium bath utilizes insoluble platinized titanium anodes, is maintained at a temperature of about 150-170 deg F, a pH of about 1.0-2.0, and contains about 3 grams per liter of ruthenium. A
ruthenium layer of an average thickness of about 10 millionths of an inch is deposited over the palladium layer. The escutcheons are then thoroughly rinsed and dried.
The ruthenium plated escutcheons are placed ir1 a sputter ion plating vessel. This vessel is a stainless steel vacuum vessel marketed by Leybold A.G. of Germany. The vessel is generally a cylindrical enclosure containing a vacuum chamber which is adapted to be evacuated by means of pumps. A source of argon gas is connected to the chamber by an adjustable valve for varying the rate of flow of argon into the chamber. In addition, two sources of nitrogen gas are connected to the chamber by an adjustable valve for varying the rate of flow of nitrogen into the chamber.
Two pairs of magnetron-type target assemblies are mounted in a spaced apart relationship in the chamber and connected to negative outputs of variable D.C. power supplies. ~ The targets constitute cathodes and the chamber wall is an anode common to the target cathodes. The target material comprises zirconium.
A substrate carrier which carries the substrates, i.e., escutcheons, is provided, e.g., it may be suspended from the top of the chamber, and is rotated by a variable speed motor to carry the substrates between each pair of magnetron target assemblies. The 219~~~9 carrier is conductive and is electrically connected to the negative output of a variable D.C. power supply.
The ruthenium plated escutcheons are mounted onto the substrate carrier in the sputter ion plating vessel. The vacuum chamber is evacuated to a pressure of about 5x10'3 millibar and is heated to about 400oC via a radiative electric resistance heater.
The target material is sputter cleaned to remove contaminants from its surface. Sputter cleaning is carried out for about one half minute by applying power to the cathodes sufficient to achieve a current flow of about 18 amps and introducing argon gas at the rate of about 200 standard cubic centimeters per minute. A pressure of about 3x10'3 millibars is maintained during sputter cleaning.
The escutcheons are then cleaned by a low pressure etch process. The low pressure etch process is carried on for about five minutes and involves applying a negative D.C. potential which increases over a one minute period from about 1200 to about 1400 volts to the escutcheons and applying D.C. power to the cathodes to achieve a current flow of about 3.6 amps. Argon gas is introduced at a rate which increases over a one minute period from about 800 to about 1000 standard cubic centimeters per minute, and the pressure is maintained at about 1.1x10' millibars. The escutcheons are rotated between the magnetron target assemblies at a rate of one revolution per minute. The escutcheons are then subjected to a high pressure etch cleaning process for about 15 minutes. In the high pressure etch process argon gas is introduced into the vacuum chamber at a rate which increases over a 10 minute period from ~? 9359 about 500 to 650 standard cubic centimeters per minute (i.e., at the beginning the flow rate is 500 sccm and after ten minutes the flow rate is 650 sccm and remains 650 sccm during the remainder of the high pressure etch process), the pressure is maintained at about 2x10'1 millibars, and a negative potential which increases over a ten minute period from about 1400 to 2000 volts is applied to the escutcheons. The escutcheons are rotated between the magnetron target assemblies at about one revolution per minute.
The pressure in the vessel is maintained at about 2x10'1 millibar.
The escutcheons are then subjected to another low pressure etch cleaning process for about five minutes. During this low pressure etch cleaning process a negative potential of about 1400 volts is applied to the escutcheons, D.C. power is applied to the cathodes to achieve a current flow of about 2.6 amps, and argon gas is introduced into the vacuum chamber at a rate which increases over a five minute period from about 800 sccm (standard cubic centimeters per minute) to about 1000 sccm. The pressure is maintained at about 1.1x10'2 millibar and the escutcheons are rotated at about one rpm.
The target material is again sputter cleaned for about one minute by applying power to the cathodes sufficient to achieve a current flow of about 18 amps, introducing argon gas at a rate of about 150 sccm, and maintaining a pressure of about 3x10'3 millibars.
21.93559 During the cleaning process shields are interposed between the escutcheons and the magnetron target assemblies to prevent deposition of the target material onto the escutcheons.
The shields are removed and a layer of zirconium having an average thickness of about 3 millionths (0.000003) of an inch is deposited on the ruthenium layer of the escutcheons during a four minute period. This sputter deposition process comprises applying D.C. power to the cathodes to achieve a current flow of about 18 amps, introducing argon gas into the vessel at about 450 sccm, maintaining the pressure in the vessel at about 6x10'3 millibar, and rotating the escutcheons at about 0.7 revolutions per minute.
After the zirconium layer is deposited a zirconium nitride layer having an average thickness of about 14 millionths (0.000014) of an inch is deposited on the zirconium layer by reactive ion sputtering over a 14 minute period. A negative potential of about 200 volts D.C. is applied to the escutcheons while D.C. power is applied to the cathodes to achieve a current flow of about 18 amps.
Argon gas is introduced at a flow rate of about 500 sccm. Nitrogen gas is introduced into the vessel from two sources. One source introduces nitrogen at a generally steady flow rate of about 40 sccm. The other source is variable. The variable source is regulated so as to maintain a partial ion current of 6.3x10'11 amps, with the variable flow of nitrogen being increased or decreased as necessary to maintain the partial ion current at this predetermined value.
~193~5~
The pressure in-the vessel is maintained at about 7.5x10'3 millibar.
The zirconium-nitride coated escutcheons are then subjected to low pressure cool down, where the heating is discontinued, pressure is increased from about 1.1x10'z millibar to about 2x10'1 millibar, and argon gas is introduced at a rate of 950 sccm.
Although the present invention has been ~ described in conjunction with a preferred embodiment, it is to be understood that modifications and variations may be resorted to without departing from the spirit and scope of the invention as those skilled in the art will readily understand. Such modifications and variations are considered to be within the purview and scope of the invention and appended claims.
Claims (42)
1. An article comprising a metallic substrate having disposed on at least a portion of its surface a multi-layer coating simulating brass comprising:
at least one layer comprised of nickel over at least a portion of said surface of said substrate;
a layer comprised of palladium over at least a portion of said layer comprised of nickel;
a layer comprised of ruthenium over at least a portion of said layer comprised of palladium;
a layer comprised of zirconium or titanium over at least a portion of said layer comprised of ruthenium;
and a layer comprised of zirconium compound or titanium compound over at least a portion of said layer comprised of zirconium or titanium.
at least one layer comprised of nickel over at least a portion of said surface of said substrate;
a layer comprised of palladium over at least a portion of said layer comprised of nickel;
a layer comprised of ruthenium over at least a portion of said layer comprised of palladium;
a layer comprised of zirconium or titanium over at least a portion of said layer comprised of ruthenium;
and a layer comprised of zirconium compound or titanium compound over at least a portion of said layer comprised of zirconium or titanium.
2. The article of claim 1 wherein said layer comprised of nickel is comprised of bright nickel.
3. The article of claim 2 wherein said layer comprised of zirconium or titanium is comprised of zirconium.
4. The article of claim 3 wherein said layer comprised of zirconium compound or titanium compound is comprised of zirconium compound.
5. ~The article of claim 4 wherein said zirconium compound is zirconium nitride.
6. ~The article of claim 1 wherein said layer comprised of zirconium or titanium is comprised of zirconium.
7. ~The article of claim 6 wherein said layer comprised of zirconium compound or titanium. compound is comprised of zirconium compound.
8. ~The article of claim 7 wherein said zirconium compound is comprised of zirconium nitride.
9. ~The article of claim 8 wherein said metallic substrate is comprised of brass.
10. ~The article of claim 1 wherein said metallic substrate is comprised of brass.
11. ~An article comprising a substrate having on at least a portion of its surface a coating simulating brass which comprises a first layer comprised of nickel;
a second layer on at least a portion of said first layer comprised of palladium;
a third layer on at least a portion of said second layer comprised of ruthenium;
a fourth layer on at least a portion of said third layer comprised of zirconium or titanium; and a fifth layer on at least a portion of said fourth layer comprised of a zirconium compound or titanium compound.
a second layer on at least a portion of said first layer comprised of palladium;
a third layer on at least a portion of said second layer comprised of ruthenium;
a fourth layer on at least a portion of said third layer comprised of zirconium or titanium; and a fifth layer on at least a portion of said fourth layer comprised of a zirconium compound or titanium compound.
12. The article of claim 11 wherein said substrate is comprised of brass.
13. The article of claim 12 wherein said first layer is comprised of bright nickel.
14. The article of claim 13 wherein said fourth layer is comprised of zirconium.
15. The article of claim 14 wherein said fifth layer is comprised of zirconium compound.
16. The article of claim 15 wherein said fifth layer is comprised of zirconium nitride.
17. The article of claim 16 wherein said substrate is brass.
18. The article of claim 11 wherein said fourth layer is comprised of zirconium.
19 19. The article of claim 18 wherein said fifth layer is comprised of zirconium compound.
20. The article of claim 17 wherein said zirconium is comprised of zirconium nitride.
21. An article comprising a metallic substrate having disposed on at least a portion of its surface a multi-layer coating comprising:
a first layer comprised of nickel;
a second layer comprised of palladium;
a third layer comprised of ruthenium;
a fourth layer comprised of zirconium or titanium; and a fifth layer comprised of zirconium compound or titanium compound.
a first layer comprised of nickel;
a second layer comprised of palladium;
a third layer comprised of ruthenium;
a fourth layer comprised of zirconium or titanium; and a fifth layer comprised of zirconium compound or titanium compound.
22. The article of claim 21 wherein said layer comprised of nickel is comprised of bright nickel.
23. The article of claim 22 wherein said layer comprised of zirconium or titanium is comprised of zirconium.
24. The article of claim 23 wherein said layer comprised of zirconium compound or titanium compound is comprised of zirconium compound.
25. The article of claim 24 wherein said zirconium compound is comprised of zirconium nitride.
26. The article of claim 25 wherein said metallic substrate is comprised of brass.
27. The article of claim 21 wherein said substrate is comprised of brass.
28. The article of claim 21 wherein said layer comprised of zirconium or titanium is comprised of zirconium.
29. The article of claim 28 wherein said layer comprised of zirconium compound or titanium compound is comprised of zirconium compound.
30. The article of claim 29 wherein said zirconium compound is comprised of zirconium nitride.
31. The article of claim 30 wherein said metallic substrate is comprised of brass.
32. An article comprising a substrate having on at least a portion of its surface a multi-layered coating comprising a first layer comprised of nickel;
a second layer on at least a portion of said first layer comprised of palladium;
a third layer on at least a portion of said second layer comprised of ruthenium;
a fourth layer on at least a portion of said third layer comprised of zirconium or titanium; and a fifth layer on at least a portion of said fourth layer comprised of a zirconium compound or titanium compound.
a second layer on at least a portion of said first layer comprised of palladium;
a third layer on at least a portion of said second layer comprised of ruthenium;
a fourth layer on at least a portion of said third layer comprised of zirconium or titanium; and a fifth layer on at least a portion of said fourth layer comprised of a zirconium compound or titanium compound.
33. ~The article of claim 32 wherein said first layer is comprised of bright nickel.
34. ~The article of claim 32 wherein said fourth layer is comprised of zirconium.
35. ~The article of claim 34 wherein said fifth layer is comprised of zirconium compound.
36. ~The article of claim 35 wherein said zirconium compound is zirconium nitride.
37. ~The article of claim 36 wherein said substrate is comprised of brass.
38. ~The article of claim 32 wherein said fourth layer is comprised of zirconium.
39. ~The article of claim 38 wherein said fifth layer is comprised of zirconium compound.
40. The article of Claim 39 wherein said zirconium compound is zirconium nitride.
41. The article of claim 40 wherein said substrate is comprised of brass.
42. The article of claim 32 wherein said substrate is comprised of brass.
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US57688695A | 1995-12-22 | 1995-12-22 | |
| US08/576,886 | 1995-12-22 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| CA2193559A1 CA2193559A1 (en) | 1997-06-23 |
| CA2193559C true CA2193559C (en) | 2002-05-28 |
Family
ID=24306415
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CA 2193559 Expired - Fee Related CA2193559C (en) | 1995-12-22 | 1996-12-20 | Substrate with protective coating thereon |
Country Status (2)
| Country | Link |
|---|---|
| CA (1) | CA2193559C (en) |
| MX (1) | MX9700185A (en) |
-
1996
- 1996-12-20 CA CA 2193559 patent/CA2193559C/en not_active Expired - Fee Related
-
1997
- 1997-01-07 MX MX9700185A patent/MX9700185A/en unknown
Also Published As
| Publication number | Publication date |
|---|---|
| CA2193559A1 (en) | 1997-06-23 |
| MX9700185A (en) | 1997-06-28 |
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