Patent Grant
10662542
This disclosure relates generally to electrodeposition processes, including electrodeposition processes that are suitable for use in the fabrication of coatings and claddings made of brass alloys that exhibit high stiffness and tensile strength.
Embodiments of this disclosure provide an electrodeposition process for forming an article, or a coating or cladding that is non-toxic or less toxic than coatings or claddings formed with toxic materials such as nickel, chromium, and alloys thereof.
Other embodiments of this disclosure provide an electrodeposition process that forms a deposited layered brass alloy having high stiffness and a high modulus of elasticity.
Other embodiments of this disclosure provide nanolaminated brass coatings on a plastic or polymeric substrate that have an ultimate tensile strength, flexural modulus, modulus of elasticity, and/or stiffness ratio that is greater than the ultimate tensile strength, flexural modulus, modulus of elasticity, and/or stiffness ratio of said conductive plastic or polymeric substrate upon which has been electrodeposited a homogenous brass coating having a thickness and composition substantially equivalent to the thickness and composition of the nanolaminated brass coating. Other embodiments describe methods for the preparation of those coatings.
Other embodiments provide an electrodeposition process that is useful for depositing a nanolaminated brass alloy coating onto a plastic or polymeric substrate at about 100 microns thick. Such coatings are useful for reinforcing plastic or polymeric substrates.
Other embodiments provide a layered brass alloy (coating) formed using an electrodeposition layering process. Where the layered brass alloy is formed on a mandrel from which it can be separated, the layered brass alloy or coating can be an article or a component of an article independent of the mandrel upon which it was formed.
Other embodiments provide an article (e.g., part) having a coating or cladding made of an electrodeposited layered brass alloy, including a coating or cladding deposited onto a plastic or polymeric substrate.
Other embodiments provide a coating or cladding that provides a protective barrier between an underlying substrate or object and an external environment or a person, serving to protect the person or environment from potential damage caused by, or a toxic property of, the substrate or object.
Other embodiments provide a coating or cladding that provides a protective barrier between an underlying substrate or object and an external environment or a person, serving to protect the substrate or object from damage, a toxic property of the external environment, wear and tear, or misuse.
Yet other embodiments of this disclosure provide electrodeposition processes that may be carried out at or near ambient temperatures. Such electrodeposition processes produce articles comprising nanolaminated brass components and/or substrates with nanolaminated brass coatings that have an increase in ultimate tensile strength, modulus of elasticity, and/or flexural modulus compared with the same component or coated substrate prepared with a homogeneous brass alloy having the same composition as the nanolaminated brass component or coating.
Electrodeposition provides a process for forming a thin coating or cladding that can reinforce or protect an underlying substrate or base component, and for forming a part or component with a coating or cladding. It has been found that an electrodeposited brass coating or cladding provides satisfactory reinforcement and protective properties, and that those properties are further enhanced when the electrodeposition forms a layered structure having multiple nanoscale layers that periodically vary in electrodeposited species or electrodeposited species microstructures. Electrodeposition also provides a process for forming (e.g., electroforming) an article comprising a component or electroforming a component, such as on a mandrel, from which it can be removed.
As a process, the use of electrodeposition to form articles/components and/or coatings having multiple laminated layers or multiple laminated “nanolayers” (i.e., nanolamination) offers a variety of advantages. Nanolamination processes enhance the overall material properties of the bulk material by providing alternating layers of differing compositions on a nano-scale that significantly increases the material properties. The material can be strengthened by controlling grain size within each laminate and by also pinning nanolayers between interfaces of dissimilar compositions. Cracks or faults that arise are forced to propagate across hundreds or thousands of interfaces, which hardens and toughens the material by hindering dislocation motion.
In an embodiment of an electrodeposition process, the electrodeposition process involves (a) placing at least a portion of a mandrel or a substrate to be coated in a first electrolyte containing metal ions of zinc and copper, and other metals as desired, (b) applying electric current and varying in time one or more of: the amplitude of the electrical current, the electrolyte temperature, an electrolyte additive concentration, or agitation of the electrolyte to produce periodic layers of electrodeposited species or periodic layers of electrodeposited species microstructures, (c) growing a nanolaminated (multilayer) coating under such conditions, and (d) optionally selectively etching the nanolaminated coating, until the desired thickness and finish of the nanolaminated coating is achieved. That process can further involve (e) removing the mandrel or the substrate from the bath and rinsing.
Electrodeposition can be conducted on a plastic or polymeric substrate that has been rendered conductive. In one embodiment, a plastic or polymeric substrate is rendered conductive by electroless metal deposition. Thus, for example, electroless copper can be applied to a plastic such as a polyamide plastic substrate in order to render the polyamide substrate conductive for subsequent electrodeposition processes. In one embodiment, electroless copper can be applied as a 2-3 micron layer onto a polymer frame. In other embodiments, non-conductive substrates such as plastic or polymeric substrates can be made conductive by application of any suitable metal by electroless processes including, but not limited to, electroless application of: nickel (see, e.g., U.S. Pat. No. 6,800,121), platinum, silver, zinc or tin.
In other embodiments a substrate formed from a non-conductive plastic or polymeric substance can be rendered conductive by the incorporation of conductive materials, such as graphite, into the plastic or polymeric composition (see, e.g., U.S. Pat. No. 4,592,808 for graphite reinforced epoxy composites).
Where necessary or desirable, substrates, and particularly plastic substrates, may be roughened to increase the adherence and/or peel resistance. Roughening may be accomplished by any relevant means including abrading the surface by sanding or sandblasting. Alternatively, surfaces, and particularly plastic surfaces, may be etched with various acids, or bases. In addition, etching processes using ozone (see e.g., U.S. Pat. No. 4,422,907), or vapor-phase sulphonation processes may be employed.
In one embodiment, where electrodeposition is to be conducted on a plastic or polymeric substrate, the plastic or polymeric substrate may comprise one or more of: ABS, ABS/polyamide blend, ABS/polycarbonate blend, a polyamide, a polyethyleneimine, a poly ether ketone, a polyether ether ketone, a poly aryl ether ketone, an epoxy, an epoxy blend, a polyethylene, a polycarbonate or mixtures thereof. In an embodiment, the process involves the electrodeposition of a layered zinc and copper alloy (brass alloy) onto a plastic substrate. The process involves first providing a basic electrolyte containing a copper salt and a zinc salt. The electrolyte can be a cyanide-containing electrochemical deposition bath. Next, a conductive polymeric substrate, upon which zinc, copper, and alloys thereof may be electrodeposited is provided, and at least a portion of the substrate is immersed in the electrolyte. A varying electric current is then passed through the immersed portion of the substrate. The electric current is controlled between a first electrical current that is effective to electrodeposit an alloy that has a specific concentration of zinc and copper and another electrical current that is effective to electrodeposit another alloy of zinc and copper. This varying electrical current may be repeated or additional electrical currents that are effective to electrodeposit other alloys of zinc and copper may be applied. The varying electric currents thereby produce a layered alloy having adjacent layers of different brass alloys on the immersed surface of the substrate or mandrel. A finishing waveform, which may include a reverse pulse, may be introduced in order to improve the surface finish as well as change the relative alloy composition at the surface.
In another embodiment, the electric current may be controlled between a first sequence of electrical pulses that is effective to electrodeposit an alloy that has a specific concentration of zinc and copper and a specific roughness, and another series of electrical pulses that is effective to electrodeposit another alloy of zinc and copper and a specific roughness. These distinct pulse sequences may be repeated to produce an electrodeposit with overall thickness that is greater than 5 microns. Any of the distinct sequences of electric pulses may include a reverse pulse that serves to reduce the surface roughness, to reactivate the surface of the electrodeposit or to permit the deposition of a brass laminate with thickness greater than 5 microns and with a substantially smooth surface.
In another embodiment, a process of electrodepositing multiple layers of brass as an article or component of an article (e.g., formed on a mandrel) or as a coating comprises: (a) providing a mandrel or a plastic or polymeric substrate treated to render it a conductive plastic or polymeric substrate; (b) contacting at least a portion of the mandrel or the conductive plastic or polymeric substrate with an electrolyte containing metal ions of zinc and copper, and optionally containing additional metal ions , wherein said conductive media is in contact with an anode; and (c) applying an electric current across the mandrel or the plastic or polymeric substrate and the anode and varying in time one or more of: the amplitude of the electrical current, electrolyte temperature, electrolyte additive concentration, or electrolyte agitation, in order to produce the nanolaminated brass coating having a desired thickness and periodic layers of electrodeposited species and/or periodic layers of electrodeposited species microstructures on the mandrel or as a coating on the plastic or polymeric substrate.
The electrodeposition can be controlled by, among other things, the application of current in the electrodeposition process. The current may be applied continuously or, alternatively, according to a predetermined pattern such as a waveform. In particular, the waveform (e.g., sine waves, square waves, sawtooth waves, or triangle waves) may be applied intermittently to promote the electrodeposition process, to intermittently reverse the electrodeposition process, to increase or decrease the rate of deposition, to alter the composition of the material being deposited, and/or to provide for a combination of such techniques to achieve a specific layer thickness or a specific pattern of differing layers. The current density (or the voltage use for plating) and the period of the waveforms may be varied independently and need not remain constant during the plating of different layers, but may be increased or decreased for the deposition of different layers. For example, current density may be continuously or discretely varied within the range between 0.5 and 2000 mA/cm2. Other ranges for current densities are also possible, for example, a current density may be varied within the range between: about 1 and 20 mA/cm2, about 5 and 50 mA/cm2, about 30 and 70 mA/cm2, 1 and 25 mA/cm2, 25 and 50 mA/cm2, 50 and 75 mA/cm2, 75 and 100 mA/cm2, 100 and 150 mA/cm2, 150 and 200 mA/cm2, 200 and 300 mA/cm2, 300 and 400 mA/cm2, 400 and 500 mA/cm2, 500 and 750 mA/cm2, 750 and 1000 mA/cm2, 1000 and 1250 mA/cm2, 1250 and 1500 mA/cm2, 1500 and 1750 mA/cm2, 1750 and 2000 mA/cm2, 0.5 and 500 mA/cm2, 100 and 2000 mA/cm2, greater than about 500 mA/cm2, and about 15 and 40 mA/cm2 based on the surface area of the substrate or mandrel to be coated. In another example, the frequency of the waveforms may be from about 0.01 Hz to about 50 Hz. In yet other examples, the frequency can be from: about 0.5 to about 10 Hz, 0.5 to 10 Hz, 10 to 20 Hz, 20 to 30 Hz, 30 to 40 Hz, 40 to 50 Hz, 0.02 to about 1 Hz, about 2 to 20 Hz, or about 1 to about 5 Hz. In one embodiment the method used to prepare the nanolaminated brass coatings on a mandrel or plastic or polymeric substrate comprises (i) applying a first cathodic current density of about 35 to about 47 mA/cm2 for a time from about 1 to 3 sec followed by (ii) a rest period of about 0.1 to about 5 seconds; and repeating (i) and (ii) for a total time from about 2 minutes to 20 minutes. Following the application of the first cathodic current, the method continues with the steps of (iii) applying a second cathodic current from about 5 to 40 mA/cm2 for about 3 to about 18 seconds, followed by (iv) applying a third cathodic current of about 75 to about 300 mA/cm2 for about 0.2 to about 2 second, which is followed by (v) an anodic current about −75 to about −300 mA/cm2 for about 0.1 to about 1 second; and repeating (iii) to (v) for time from about 3 to about 9 hours. The process may be repeated to obtain multiple layers of nanolaminated brass coatings. For example by repeating steps (i)-(v) as described above.
The electrical potential may also be varied to control layering and the composition of individual layers. For example, an electrical potential employed to prepare the coatings may be in the range of 0.5 V and 20 V. In another example, the electrical potential may be within a range selected from 1 V to 20 V, 0.50 to 5 V, 5 to 10 V, 10 to 15 V, 15 to 20 V, 2 to 3 V, 3 to 5 V, 4 V to 6 V, 2.5V to 7.5 V, 0.75 to 5 V, 1 V to 4 V, and 2 to 5 V.
In an embodiment, of the coating or cladding, an electrodeposited, layered brass alloy is formed to have multiple nanoscale layers that periodically vary in electrodeposited species or electrodeposited microstructures, with variations in the layers of electrodeposited species or electrodeposited species microstructure providing a material with high modulus of elasticity. Another embodiment provides an electrodeposition process that forms a laminated brass alloy that varies in the concentration of alloying elements from layer-to-layer. Yet another embodiment is an electrodeposited, nanolaminated brass alloy coating or bulk material having multiple nanoscale layers that vary in electrodeposited species microstructure with layer variations resulting in a material with a high modulus of elasticity.
In another embodiment, a nanolaminated component or coating having a plurality of layers of brass alloys is provided. The layers are of the same thickness or of different thicknesses. Each of the layers, referred to herein as nanoscale layers and/or periodic layers, has a thickness of from approximately 2 nm to approximately 2,000 nm.
In one embodiment, a brass component comprised of nanolaminated brass exhibits an ultimate tensile strength that is at least 10%, 20% or 30% greater than a brass component formed from a homogeneous brass alloy that has a composition substantially equivalent to the composition of said nanolaminated brass coating.
In another embodiment, a plastic or polymeric substrate, or a portion thereof, can be coated with a nanolaminated brass coating. The coated substrate is stronger than the uncoated substrate or the substrate when coated with a homogeneous brass alloy that has a thickness and composition substantially equivalent to (or equivalent to) the thickness and composition of the nanolaminated brass coating. In some embodiments the ultimate tensile strength of the coated plastic or polymeric substrate is increased by greater than 10, 20, or 30% relative to the homogeneously coated plastic or polymeric substrate. In other embodiments the ultimate tensile strength of the coated plastic or polymeric substrate is increased by greater than 100%, 200%, 300%, 400% or 500% relative to the uncoated plastic or polymeric substrate.
In one embodiment, a nanolaminated brass coating present on a plastic or polymeric substrate exhibit more than a three-fold increase in flexural modulus relative to said plastic or polymeric substrate without said coating, when the nanolaminated brass coating has a cross-sectional area of 5% of the total cross-sectional area of the coated substrate. In another embodiment, a nanolaminated brass coating present on a plastic or polymeric substrate provides more than a four-fold increase in flexural modulus relative to the plastic or polymeric substrate without the coating, when the nanolaminated brass coating has a cross-sectional area of 10%.
In other embodiments, components comprised of nanolaminated brass have a modulus of elasticity greater than about 60, 65, 70, 75, 80, 90, 100, 110, 120, 130, 140, 150, 160, 180, 200, 220, 240, 250, or 300 GPa. In another embodiment, the nanolaminated brass coating has a modulus of elasticity greater than 60, 65, 70, 75, 80, 90, 100, 110, 120, 130, 140, 150, 160, 180, 200, 220, 240, 250, or 300 GPa. In another embodiment, the nanolaminated brass component or the nanolaminated brass coating has a modulus of elasticity expressed in giga Pascals (GPa) from about 60 to about 100, or from about 80 to about 120, or from about 100 to about 140, or from about 120 to about 140, or from about 130 to about 170, or from about 140 to about 200, or from about 150 to about 225, or from about 175 to about 250, or from about 200 to about 300 GPa.
In one embodiment, the coating increases the stiffness of a plastic or polymeric substrate. In such an embodiment, relative to an uncoated substrate, a nanolaminated brass-coated plastic or polymeric substrate exhibits more than about a 2.8-fold increase in stiffness when the nanolaminated brass coating has a cross-sectional area of about 10% of the total cross-sectional area of the coated substrate. In another embodiment, a more than 4-fold increase in stiffness is observed when said coating has a cross-sectional area of about 15% of the total cross-sectional area of the coated substrate. In another embodiment, a more than 7-fold increase in stiffness is observed when said coating has a cross-sectional area of about 20% of the total cross-sectional area of the coated substrate.
In one embodiment, where a nanolaminated brass coating is present on at least a portion of a surface of a plastic or polymeric substrate, the article, or the portion of the article bearing the coating, exhibits an ultimate tensile strength that is at least 267% greater than the uncoated substrate. In another embodiment, the article is a nanolaminated brass-coated plastic or polymeric substrate that exhibits an ultimate tensile strength that is at least 30% greater than the ultimate tensile strength of the plastic or polymeric substrate coated with a homogeneous brass alloy that has a thickness and composition substantially equivalent to the thickness and composition of said nanolaminated brass coating.
As used herein a thickness is substantially equivalent to one or more other thickness(es) if it is with the range from 95% to 105% of the one or more other thickness(es).
As used herein, a composition is substantially equivalent to a nanolaminated brass coating composition when (i) it contains all of the components of the nanolaminate brass coating that are present at more than 0.05 weight percent (i.e., 0.5% based on the weight of the nanolaminate coating) and (ii) each said component is present in an amount that is from 95% to 105% of the weight percent appearing in the nanolaminate brass coating. For example, if a component of a nanolaminate coating is present at about 2% by weight (based on the weight and composition of all layers of the nanolaminate coating) then in an equivalent composition (e.g., a homogeneous coating) the component would be required to be present in an amount from 1.9% to 2.1% by weight.
The electrodeposition process can be controlled to selectively apply coating to only portions of the substrate. For example, a masking product can be applied with a brush or application technique to cover portions of the substrate to prevent coating during a subsequent electrodeposition process.
Embodiments of the method can be conducted at or near ambient temperatures, i.e., temperatures of approximately 20 degrees C., to temperatures of approximately 155 degrees C. Conducting the electrodeposition of the nanolaminated coating at or near ambient temperatures reduces the likelihood of introducing flaws as a result of temperature-related deformation of a polymeric substrate or mandrel onto which the alloy is deposited.
As used herein, “metal” means any metal, metal alloy or other composite containing a metal. In an example, these metals may comprise one or more of Ni, Zn, Fe, Cu, Au, Ag, Pt, Pd, Sn, Mn, Co, Pb, Al, Ti, Mg, and Cr. When metals are deposited, the percentage of each metal may independently be selected. Individual metals may be present at about 0.001, 0.005, 0.01, 0.05, 0.1, 0.5, 1, 5, 10, 15, 20, 25, 30, 30, 35, 40, 45, 50, 55, 60, 65, 70, 75, 80, 85, 90, 95, 98, 99, 99.9, 99.99, 99.999, or 100 percent of the electrodeposited species/composition.
The nanolaminated brass described herein comprises layers (periodic layers) with a zinc content that varies between 1% and 90% and a copper content that varies between 10 and 90% on a weight basis. In one embodiment, at least one of the periodic layers comprises a brass alloy with a zinc concentration that varies between 1% and 90%. In another embodiment, at least half of the periodic layers comprise a brass alloy with a zinc concentration that varies between 1% and 90%. In another embodiment, all of the periodic layers comprise a brass alloy with a zinc concentration that varies between 1% and 90%. In one embodiment, the zinc content is about 50% to about 68%, about 72% to about 80%, about 60% to about 80%, about 65% to about 75%, about 66% to about 74%, about 68% to about 72%, about 60%, about 65%, about 70%, about 75% or about 80% by weight. Where additional metals or metalloids (such as silicon) are present in one or more layers (periodic layers) of said nanolaminated brass articles/components or coatings, the additional metals will typically comprise between 0.01% and 15% of the layer composition by weight. In one embodiment, the total amount of additional metals and/or metalloids is less than 15%, 12%, 10%, 8%, 6%, 5%, 4%, 3%, 2%, 1%, 0.5%, 0.2%, 0.1%, 0.05%, or 0.02% but in each instance greater than about 0.01% by weight.
In an embodiment, the coating can have a coating thickness that varies according to properties of the material that is to be protected by the coating, or according to the environment to which the coating is subjected. In one embodiment the overall thickness of the nanolaminated brass coating (e.g., the desired thickness) is between 10 nanometers and 100,000 nanometers (100 microns), 10 nanometers and 400 nanometers, 50 nanometers and 500 nanometers, 100 nanometers and 1,000 nanometers, 1 micron to 10 microns, 5 microns to 50 microns, 20 microns to 200 microns, 40 microns to 100 microns, 50 microns to 100 microns, 50 microns to 150 microns, 60 microns to 160 microns, 70 microns to 170 microns, 80 microns to 180 microns, 200 microns to 2 millimeters (mm), 400 microns to 4 mm, 200 microns to 5 mm, 1 mm to 6.5 mm, 5 mm to 12.5 mm, 10 mm to 20 mm, and 15 mm to 30 mm.
In an embodiment, the coating is sufficiently thick to provide a surface finish. In one embodiment, the overall thickness of a nanolaminated brass coating on a plastic substrate is between 50 and 90 microns. In another embodiment, the overall thickness of a nanolaminated brass coating on a plastic substrate is between 40 and 100 microns or 40 and 200 microns. The surface finish can be modified by polishing methods, such as mechanical polishing, electropolishing, and acid exposure. The polishing can be mechanical and remove less than approximately 20 microns from the coating thickness. In one embodiment, the thickness of the brass coating on a plastic or polymeric substrate is less than 100 microns, for example, ranging between 45 and 80 microns across the layers of the coating and, for example, providing an average thickness of 70-80 microns. In one embodiment, the nanolaminated brass coating is polished or electropolished to a surface having an arithmetic average roughness (Ra) less than about 25, 12, 10, 8, 6, 4, 2, 1, 0.5, 0.2, 0.1, 0.05, 0.025, or 0.01 microns. In another embodiment, the average surface roughness is less than about 4, 2, 1, 0.5, 0.2, 0.1, 0.05, 0.025, or 0.01 microns. In another embodiment, the average surface roughness is less than about 2, 1, 0.5, 0.2, 0.1, or 0.05 microns
Nanolaminated brass coatings, articles or components of articles may contain any number of desired layers (e.g., 2 to 100,000 layers) of suitable thickness. In some embodiments the coatings will comprise 2, 3, 4, 5, 6, 7, 8, 9, 10, 12, 14, 16, 18, 20, 22, 24, 26, 28, 30, 35, 40, 45, 50, 60, 70, 80, 90, 100, 150, 200, 250, 300, 350, 400, 450, 500, 600, 700, 800, 900, 1,000, 1,500, 2,000, 2,500, 3,000, 4,000, 5,000, 7,500, 1,000, 2,000, 4,000, 6,000, 8,000, 10,000, 20,000, 40,000, 60,000, 80,000, or 100,000 or more layers of electrodeposited materials, where each layer may be from about 2 nm-2,000nm (2 microns). In some embodiments, the individual layers have a thickness from about 2 nm-10 nm, 5 nm-15 nm, 10 nm -20 nm, 15 nm-30 nm, 20 nm-40 nm, 30 nm-50 nm, 40 nm-60 nm, 50 nm-70 nm, 50 nm-75nm, 75 nm-100 nm, 5 nm-30 nm, 15 nm-50 nm, 25 nm-75 nm, or 5 nm-100 nm. In other embodiments, the individual layers have a thickness of about 2 nm to 1,000 nm, or 5 nm to 200 nm, or 10 nm to 200 nm, or 20 nm to 200 nm, 30 nm to 200 nm, or 40 nm to 200 nm, or 50 nm to 200 nm.
Nanolaminated brass coatings, articles, or components of articles, may contain a series of layers that may be organized in a variety of ways. In some embodiments, layers that differ from each other in the electrodeposited species (metal and/or metalloid composition) and/or the microstructure of the electrodeposited species are deposited in repeated patterns. Although a type of layer may recur more than once in a coating or article, the thickness of that type of layer may or may not be the same in each instance where it appears. Nanolaminated brass coatings, articles, or components of articles may comprise two, three, four, five or more types of layers that may or may not repeat in a specific pattern.
By way of non-limiting example, layers designated a, b, c, d, and e that differ in the electrodeposited species (metal and/or metalloid composition) and/or the microstructure of the electrodeposited species may be organized in an alternating pattern such as a binary (a,b,a,b,a,b,a,b, . . . ), ternary (a,b,c,a,b,c,a,b,c,a,b,c, . . . ), quaternary (a,b,c,d,a,b,c,d,a,b,c,d,a,b,c,d, . . . ), quinary (a,b,c,d,e,a,b,c,d,e,a,b,c,d,e,a,b,c,d,e, . . . ) and so on. Other arrangements are also possible such as (c,a,b,a,b,c,a,b,a,b,c, . . . ), (c,a,b,a,b,e,c,a,b,a,b,e, . . . ) etc.
In some embodiments the nanolaminated brass prepared by the methods of electrodeposition described herein comprises 2, 3, 4, 5, or 6 or more layers of different composition having different electrodeposited species and/or different amounts of electrodeposited species. In some embodiments the nanolaminated brass prepared by the methods of electrodeposition described herein comprises 2, 3, 4, 5, 6 or more layers with different microstructures.
In other embodiments, the nanolaminated brass comprises a combination of different layers that have different compositions and different microstructures. Thus, for example, in some embodiments, the nanolaminated brass coatings and components prepared as described herein have a first layer and contain (i) at least one layer that differs from the first layer in the amounts/types of electrodeposited species, and (ii) at least one layer that differs from the first layer in microstructure, where the layers differing in electrodeposited species and microstructure may be the same or different layers.
In some embodiments, the nanolaminated brass has a first layer and contains (i) at least two layers that differ from the first layer and each other in the amounts and/or types of electrodeposited species, and (ii) at least one layer that differs from the first layer in microstructure. In some embodiments, the nanolaminated brass has a first layer and contains at least (i) one layer that differs from the first layer in the amounts and/or types of electrodeposited species, and (ii) at least two layers that differ from the first layer and each other in microstructure. In other embodiments, the nanolaminated brass has a first layer and contains (i) at least two layers that differ from the first layer, and each other in the amounts and/or types of electrodeposited species, and (ii) at least two layers that differ from the first layer and each other in microstructure. In each instance, the layers differing in electrodeposited species and/or microstructure may be the same or different layers.
In other embodiments, the nanolaminated brass has a first layer and contains (i) at least three layers that differ from the first layer and each other in the amounts and/or types of electrodeposited species, and (ii) at least two layers that differ from the first layer and each other in microstructure. In other embodiments, the nanolaminated brass has a first layer and contains (i) at least two layers that differ from the first layer and each other in the amounts and/or types of electrodeposited species, and (ii) at least three layers that differ from the first layer and each other in microstructure. In other embodiments, the nanolaminated brass has a first layer and contains (i) at least three layers that differ from the first layer and each other in the amounts and/or types of electrodeposited species, and (ii) at least three layers that differ from the first layer and each other in microstructure. In each instance, the layers differing in electrodeposited species and/or microstructure may be the same or different layers
In other embodiments, the nanolaminated brass has a first layer and contains (i) at least four layers that differ from the first layer and each other in the amounts and/or types of electrodeposited species, and (ii) at least four layers that differ from the first layer and each other in the first layer in microstructure. In other embodiments, the nanolaminated brass has a first layer and contains (i) at least five layers that differ from the first layer and each other in the amounts and/or types of electrodeposited species, and (ii) at least five layers that differ from the first layer and each other in the first layer in microstructure. In each instance, the layers differing in electrodeposited species and/or microstructure may be the same or different layers
The following example describes a method for the preparation of an electrodeposited nanolaminated brass coating or cladding that can be deposited on a plastic or polymeric substrate.
Prior to the electrolytic deposition of any metals on the surface of a plastic or polymeric substrate the substrate is electrolessly plated with a commercial electroless nickel (or electroless copper) solution to form a conductive coating typically 2-3 microns thick. The e-nickel coated substrate is then immersed in 50% aqueous saturated HCl (approximately 10.1% HCl) for two minutes or until bubble formation is noted. The substrate is then washed with water.
The substrate is immersed in a commercial cyanide copper-zinc electroplating bath (E-Brite B-150 Bath from Electrochemical Products Inc. (EPI)) comprising CuCN (29.95 g/l), ZnCN (12.733 g/l), free cyanide (14.98 g/l), NaOH (1.498 g/l), Na2CO3 (59.92 g/l) E-Brite™ B-150 1% by volume, Electrosolv™ 5% by volume, E-Wet™ 0.1% by volume. The pH of the bath ranged from 10.2 to 10.4, temperature for plating was from 90-120 degrees F. The anode to cathode ratio was from 2:1 to 2.6 to 1 with an anode of alloy 260 or Rolled or extruded 70/30 (copper/zinc) brass. Agitation was provided either by cathode movement at 15 ft/minute or by air sparging using a flow rate of 2 cubic feet per minute of air per foot of sparging pipe.
Electrodeposition is commenced by applying a waveform consisting of a 42.2 mA/cm2 pulse held for 1.9 seconds, followed by a 0 mA/cm2 pulse (rest period) applied for 0.25 sec. for a total of 10 minutes. Immediately following the ten minute period where the preceding waveform is applied, a second waveform is applied for 6 hours and 40 minutes, consisting of a 20 mA/cm2 pulse applied for 9 seconds, followed by a 155 mA/cm2 pulse applied for 1 sec, followed by a −155 mA/cm2 stripping (reverse) pulse applied for 0.4 seconds. During electrodeposition the anodes were cleaned as necessary to prevent the passivization of the anodes. Where necessary, anodes were cleaned at two hour intervals, which required pausing the electrodeposition process.
The process applies a nanolaminated brass coating to the substrate having a periodic layers with a thickness of 40 to 50 nm (about 44 nm). The total thickness of the coating was about 100 microns.
Nanolaminated brass-coated polymeric dog bone specimens were tested using ASTM D638. Tensile specimens were prepared by laser-cutting dog bones from acrylonitrile butadiene styrene (ABS) sheet to the geometry specified in the ASTM standard. These substrates were subsequently coated using the method described in Example 1. An Instron Model 4202 test frame was used to conduct the tensile testing.
The resulting ultimate tensile strength results are depicted in
Tensile testing also produced elastic modulus (stiffness) data.
Specimen substrates were cut from ABS sheets of differing thickness (⅛ and 1/16 of an inch) and coated as described in Example 1 with a nanolaminated brass coating 100 microns thick. The flexural modulus was tested according to ASTM D5023. The results are shown in
To quantify the difference between nanolaminated brass coating and homogeneous brass alloy coating, a control sample, in this case a plastic frame part, was electroplated using a direct current (DC) at a specified average current density. At the completion of a plating period that was sufficient to produce an 80-micron thick nanolaminated brass coating on a part produced in accordance with an embodiment, the DC control plastic frame was coated with only 30 microns of non-laminated brass. This lesser thickness of the control was due to the fact that a DC plating of brass proceeds at a significantly slower plating rate that slows and becomes thickness-limited over the time the plating proceeds. Therefore, a DC-plated homogeneous brass part could not be created at the desired thickness for comparison. Accordingly, a homogeneous (not laminated) brass-coated part was fabricated using a pulse plating technique to achieve the desired thickness of 80 microns, and to provide a homogeneous-coated part for comparison to the part with the 80-micron nanolaminated brass coating.
The homogeneous-coated part having a coating thickness of 80 microns, the part having a nanolaminated brass coating with a thickness of 80 microns, and an uncoated plastic part were evaluated and compared using ASTM D5023, modified to accommodate the unique part geometry. The load results show that, for a constant 0.10 inch deflection, the part coated with nanolaminated brass had an increase of about 270% in ultimate tensile strength relative to the uncoated part, and a 20% increase in ultimate tensile strength relative to the part with the homogenous brass coating. The test results are shown in the following table:
The load results demonstrate that layer modulation of the nanolaminated coating significantly increases the strength as compared to a homogeneous coating.
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| 20180016692 A1 | Jan 2018 | US |
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| 61366924 | Jul 2010 | US |
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| Parent | 13747020 | Jan 2013 | US |
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| Number | Date | Country | |
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| Parent | PCT/US2011/045128 | Jul 2011 | US |
| Child | 13747020 | US |
